ANIMAL CHEMISTRY, v /I £ 4 t I > I) * yf , ORGANIC CHEMISTRY I IN ITS APPLICATIONS TO PHYSIOLOaY AND PATHOLOGY. BY JUSTUS LIEBIG, M. D., Ph. D. F. R. S., M. R. I. A., PROFESSOR OF CHEMISTRY IN THE UNIVERSITY OF GIESSEN. EDITED FROM THE AUTHOR'S MANUSCRIPT, WILLIAM GREGORY, M. D., F. R. S. E., M. R. I. A. PROFESSOR OF MEDICINE AND CHEMISTRY IN THE UNIVERSITY AND KING'S COLLEGE, ABERDEEN. ybilaftelpljia: JAMES M. CAMPBELL, 98 CHESTNUT STREET. NEW YORK: SAXTON & MILES, 205 BROADWAY. STEREOTYPED BY C. W. MURRAY & CO. 1845. TO THE BRITISH ASSOCIATION FOR THE ADVANCEMENT OF SCIENCE. At the meeting of the British Association in Glasgow, in 1840,1 had the honour to present the first part of a report on the then present state of Organic Chemistry, in which I endeavoured to develope the doctrines of this science in their bearing on Agriculture and Physiology. It affords me now much gratification to be able to communicate to the meeting of the Association for the present year the second part of my labours; in which I have attempted to trace the application of Organic Chemistry to Animal Physiology and Pathology. * In the present work an extensive series of phenomena have been treated in their chemical relations; and although it would be presumptuous to consider the questions here raised as being definitely resolved, yet those who are familiar with chemistry will perceive that the only method which can lead to their final resolution, namely, the quantitative method, has been employed. The formulae and equations in the second part, therefore, although they are not to be viewed as ascertained truths, and as furnishing a complete, or the only explanation of the vital processes there treated of, are yet true in this sense: that being deduced from facts by logical induction, they must stand as long as no new facts shall be opposed to them. When the chemist shows, for example, that the elements of the bile, added to those of the urate of ammonia, correspond exactly to those of blood, he presents to us a fact which is independent of all hypothesis. It remains for the physiologist to determine, by experiment, whether the conclusions drawn by the chemist from such a fact be accurate or erroneous. And whether this question be answered in the affirmative or in the negative, the fact remains, and will some day find its true explanation. I have now to perform the agreeable duty of expressing my sense of the services rendered to me in the preparation of the English edition by my friend, Dr. Gregory. The distinguished station he occupies as a chemist; the regular education which he has received in the various branches of medicine; and his intimate acquaintance with the German language—all these, taken together, are the best securities that the translation is such as to convey the exact sense of the original; securities, such as are not often united in the same individual. It is my intention to follow this second part with a third, the completion of which, however, cannot be looked for before the lapse of two years. This third part will contain an investigation of the food of man and animals, the analysis of all articles of diet, and the study of the changes which the raw food undergoes in its preparation; as, for example, in fermentation (bread,) baking, roasting, boiling, &c. Already, it is true, many analyses have been made for the proposed work; but the number of objects of investigation is exceedingly large, and in order to determine with accuracy the absolute value of seed, or of flour, or of a species of fodder, 8cc, as food, the ultimate analysis alone is not sufficient; there are required comparative investigations, which present very great difficulties. DR. JUSTUS LIEBIG. Giessen, 3d June. 1842. . (3) NOTE. J would beg leave to refer the chemical as well as the physiological reader particularly to the analyses (in Note (27) Appendix) of the animal tissues, which ought to have been referred to on pages 21 and 42, and which at present are only referred to in Note (7.) Since the work was printed, moreover, there has been added, at the end of the Appendix, an interesting paper by Keller (see page 101,) confirming the very important observation of A. Ure, junior, as to the conversion of benzoic acid into hippuric acid in the human body; a fact which, I perceive, by the Philosophical Magazine for June, has also been confirmed by Mr. Garrod, probably at an earlier period than by M. Keller. The reader will perceive that this fact strengthens materially the argument of the Author on the action of remedies. W. G. PREFACE. By the application to chemistry of the methods which had for centuries been followed by philosophers in ascertaining the causes of natural phenomena in physics—by the observation of weight and measure—Lavoisier laid the foundation of a new science, which, having been cultivated by a host of distinguished men, has, in a sihgularly short period, reached a high degree of perfection. It was the investigation and determination of all the conditions which are essential to an observation or an experiment, and the discovery of the true .principles of scientific research, that protected chemists from error, and conducted them, by a way equally simple and secure, to discoveries which have shed a brilliant light on those natural phenomena which Were previously the most obscure and incomprehensible. The most useful applications to the arts, to industry, and to all branches of knowledge related to chemistry, sprung from the laws thus established; and this influence was not delayed till chemistry had attained its highest perfection, but came into action with each new observation. All existing experience and observation in other departments of science reacted, in like manner, on the improvement and development of chemistry; so that chemistry received from metallurgy and from other industrial arts as much benefit as she had conferred on them. While they simultaneously increased in wealth, they mutually contributed to the development of each other. After mineral chemistry had gradually attained its present state of development, the labours of chemists took a new direction. From the study of the constituent parts of vegetables and animals, new and altered views have arisen; and the present work is an attempt to apply these views to physiology and pathology. In earlier times the attempt has been made, and often with great success, to apply to the objects of the medical art the views derived from an acquaintance with chemical observations. Indeed, the great physicians, wb/o lived towards the end of the seventeenth century, were the founders of chemistry, and in those days the only philosophers acquainted with it. The phlogistic system was the dawn of a new day; it was the victory of philosophy over the rudest empiricism. With all its discoveries, modern chemistry has performed but slender services to physiology and pathology; and we cannot be deceived as to the cause of this failure, if we reflect that it was found impossible to trace any sort of relation between the observations made in inorganic chemistry, the knowledge of the characters of the elementary bodies and of such of their compounds as could be formed in the laboratory, on the one hand, and the living body, with the characters of its constituents, on the other. Physiology took no share in the advancement of chemistry, because for a long period she received from the latter science no assistance in her own development. This state of matters has been entirely changed within five and twenty years. But during this period physiology has also acquired new ways and methods of investigation within her own province; and it is only the exhaustion of these sources of a2 5 PREFACE. VI discovery which has enabled us to look forward to a change in the direction of the labours of physiologists. The time for such a change is now at hand; and a perseverance in the methods lately followed in physiology would now, from the want, which must soon be felt, of fresh points of departure for researches, render physiology more extensive, but neither more profound nor more solid. No one will venture to maintain that the knowledge of the forms and of the phenomena of motion in organized beings is either unnecessary or unprofitable. On the contrary, this knowledge must be considered as altogether indispensable to that of the vital processes. But it embraces only one class of the conditions necessary for the acquisition of that knowledge, and is not of itself sufficient to enable us to attain it. The study of the uses and functions of the different organs, and of their mutual connection in the animal body, was formerly the chief object of physiological researches ; but lately this study has fallen into the back-ground. The greater part of all the modern discoveries has served to enrich comparative anatomy far more than physiology. These researches have yielded the most valuable results in relation to the recognition of the dissimilar forms and conditions to be found in the healthy and in the diseased organism; but they have yielded no conclusions calculated to give us a more profound insight into the essence of the vital processes. The most exact anatomical knowledge of the structure of the tissues cannot teach us their uses; and from the microscopical examination of the most minute reticulations of the vessels we can learn no more as to their functions than we have learned concerning vision from counting the surfaces on the eye of the fly. The most beautiful and elevated problem for the human intellect, the discovery of the laws of vitality, cannot be resolved, nay, cannot even be imagined, without an accurate knowledge of chemical forces ; of those forces which do not act at sensible distances; which are manifested in the same way as those ultimate causes by which the vital phenomena are determined; and which are invariably found active, whenever dissimilar substances come into contact. Physiology, even in the present day, still endeavours, but always after the fashion of the phlogistic chemists (that is, by the qualitative method,) to apply chemical experience to the removal of diseased conditions; but with all these countless experiments we are not one step nearer to the causes and the essence of disease. With proposing well-defined questions, experimenters have placed blood, urine, and all the constituents of the healthy or diseased frame, in contact with acids, alkalies, and all sorts of chemical re-agents; and have drawn, from observation of the changes thus produced, conclusions as to their behaviour in the body. By pursuing this method, useful remedies or modes of treatment might by accident be discovered; but a rational physiology cannot be founded on mere re-actions, and the living body cannot be viewed as a chemical laboratory. In certain diseased conditions, in which the blood acquires a viscid consistence, this state cannot be permanently removed by a chemical action on the fluid circulating in the blood-vessels. The deposit of a sediment from the urine may, perhaps, be prevented by alkalies, while their action has not the remotest tendency to remove the cause of disease. Again, when we observe, in typhus, insoluble salts of ammonia in the fasces, and a change in the globules of the blood similar to that which may be artificially produced by ammonia, we are not, on that account, PREFACE. VII entitled to consider the presence of ammonia in the body as the cause, but only as the effect of a cause. Thus medicine, after the fashion of the Aristotelian philosophy, has formed certain conceptions in regard to nutrition and sanguification; articles of diet have been divided into nutritious and non-nutritious; but these theories, being founded on observations destitute of the conditions most essential to the drawing of just conclusions, could not be received as expressions of the truth. How clear are now to us the relations of the different articles of food to the objects which they serve in the body, since organic chemistry has applied to the investigation her quantitative method of research! When a lean goose, weighing 4 lbs., gains, in thirty-six days, during which it has been fed with 24 lbs. of maize, 5 lbs. in weight and yields 3| lbs. of pure fat, this fat cannot have been contained in the food, ready formed, because maize does not contain the thousandth part of its weight of fat, or of any substance resembling fat. ' And when a certain number of bees, the weight of which is exactly known, being fed with pure honey, devoid of wax, yield one part of wax for every twenty parts of honey consumed, without any change being perceptible in their health or in their weight, it is impossible any longer to entertain doubt as to the formation of fat from sugar in the animal body. We must adopt the method which has thus led to the discovery of the origin of fat, in the investigation of the origin and alteration of the secretions, as well as in the study of all the other phenomena of the animal body. From the moment we begin to look earnestly and conscientiously for the true answers to our questions, that we take the trouble, by means of weight and measure, to fix our observations, and express them in the form of equations, these answers are obtained without difficulty. However numerous our observations may be, yet, if they only bear on one side of a question, they will never enable us to penetrate the essence of a natural phenomenon in its full significance. If we are to derive any advantage from them, they must be directed to a well defined object; and there must be an organized connection between them. Mechanical philosophers and chemists justly ascribe to their methods of research the greater part of the success which has attended their labours. The result of every such investigation, if it bear in any degree the stamp of perfection, may always be given in few words; but these few words are eternal truths, to the discovery of which numberless experiments and questions were essential. The researches themselves, the laborious experiments and complicated apparatus, are forgotten as soon as the truth is ascertained. They were the ladders, the shafts, the tools, which were indispensable to enable us to attain to the rich vein of ore; they were the pillars and air passages which protected the mine from water and from foul air. Every chemical or physical investigation, however insignificant, which lays claim to attention, must in the present day possess this character. From a certain number of observations it must enable us to draw some conclusion, whether it be extended or limited. The imperfection of the method or system of research adopted by physiologists can alone explain the fact, that for the last fifty years they have established so few new and solid truths in regard to a more profound knowledge of the functions of the most important organs, of the spleen, of the liver, and of the numerous glands VIII PREFACE. of the body; and the limited acquaintance of physiologists with the methods of research employed in chemistry will continue to be the chief impediment to the progress of physiology, as well as a reproach which that science cannot escape, Before the time of Lavoisier, Scheele, and Priestley, chemistry was not more closely related to physics than she is now to physiology. At the present day chemistry is so fused, as it were, into physics, that it would be a difficult matter to draw the line between them distinctly. The connection between chemistry and physiology is the same, and in another half century it will be found impossible to separate them. Our questions and our experiments intersect in numberless curved linps the straight line that leads to truth. It is the points of intersection that indicate to us the true direction; but, owing to the imperfection of the human intellect, these curve lines must be pursued. Observers in chemistry and physics have the eye ever fixed on the object which they seek to attain. One may succeed, for a space, in following the direct line; but all are prepared for circuitous paths. Never doubting of the ultimate success of their efforts, provided they exhibit constancy and perseverance, their eagerness and courage are only exalted by difficulties. Detached observations, without connection, are points scattered over the plain, which do not allow us to choose a decided path. For centuries chemistry presented nothing but these points, and sufficient means were available to fill up the intervals between them. But permanent discoveries and real progress were only made when chemists ceased to make use of fancy to connect them. My object in the present work has been to direct attention to the points of intersection of chemistry with physiology, and to point out those parts in which the sciences become, as it were, mixed up together. It contains a collection of problems, such as chemistry at present requires to be resolved; and a number of conclusions drawn according to the rules of that science from such observations as have been made. These questions and problems will be resolved: and we cannot doubt that we shall have in that case a new physiology and a rational pathology. Our sounding line, indeed, is not long enough to measure the depths of the sea, but is not on that account less valuable to us: if it assist us, in the mean time, to avoid rocks and shoals, its use is sufficiently obvious. In the hands of the physiologist, organic chemistry must become an intellectual instrument, by means of which he will be enabled to trace the causes of phenomena invisible, to the bodily sight; and if among the results which I have developed or indicated in this work, one alone shall admit of a useful application, I shall consider the object for which it was written as fully attained. The path which has led to it will open up other paths; and this I consider as the most important object to be gained. JUSTUS LIEBIG. Giessen, April, 1842. 2 IX CONTENTS. Origin of bile in the herbivora . . 47 Origin of bile in the carnivora . . 47 Formation of gelatine . . . .46 Relation of blood or flesh and proteine to the secretions and excretions . 45 The constituents of the urine derived from the metamorphosed tissues . 45 Metamorphoses of blood and flesh . 44 Formula of blood and metamorphoses of bile 44 The secretions contain all the elements of the blood 43 Gelatine contains no proteine, although formed from it 42 Composition of the animal tissues . 42 Composition of proteine . . .41 Source of the nitrogen exhaled from the lungs and skin . . . .39 Use of the saliva 38 Theory of chymification . . .37 It is formed by vegetables alone . . 37 THE METAMORPHOSIS OF TISSUES. Discovery of proteine . . . .36 PART II. But it may serve to nourish the gelatinous tissues 35 Gelatine incapable of serving for nutrition, strictly so called . . .35 Elements of nutrition and of respiration 35 It is formed when oxygen is deficient, and is a source of animal heat. . 33 Its formation is a source of oxygen . 32 Origin of fat in domesticated animals . 31 Assimilation less energetic in the carnivora 31 Importance of agriculture to population 30 Waste of matter very rapid in carnivora 30 The same is true of the class of herbivora 28 The butter, sugar, &c, of its food support respiration . . . .28 Assimilation more energetic in the young animal 27 Amount of bile secreted . . .27 True function of the bile . . .26 The carbon is consumed or burned . 26 Nitrogen in the urine . ... 25 Carbon accumulates in the bile . . 25 Changes of the food in the organism of carnivora 24 Uses of the non-azotized ingredients of food . . . . . .23 The blood of animals is therefore formed by vegetables 23 These products identical with the constituents of blood . . . .22 In the herbivora, depends on the azotized products of vegetables . . 22 Nutrition in the carnivora the most simple 22 Identity of organic composition in fibrine and albumen 21 Nutrition depends on the constituents of blood . ... . . . 21 Nervous and vegetative life . . .20 Amount of animal heat . . .19 Nerves and muscles not the source of animal body , 18 Cause of death in starvation and chronic diseases 17 The process of starvation . . .17 Effects of climate on the appetite . 16 The amount of oxygen regulates that of food. 16 The mutual action of oxygen and carbon in the body is the true source of animal heat 15 Effect of heat on these variations. . 15 The consumption of oxygen varies . 14 in the body 14 It combines with carbon and hydrogen Amount of oxygen inspired by an adult man .14 Nutrition depends on chemical changes 13 Conditions of animal life . . .13 Laws of the vital force . . .13 Vitality independent of consciousness . 12 A ssimilation the result of chem ical forces 12 Distinction between animal and vegetable life 11 Vital force, vis vita% or vitality . .11 PART I. CONTENTS X I Page Phosphorus seems essential to nervous matter 59 Origin of hippuric acid . . .48 Formation of the chief secretions and excretions 48 PART III. Soda essential to the bile . . .49 1. The phenomena of motion in the animal organism . . . .60 Relation of urine to bile . . .50 Relation of starch to bile . . .51 2. The same subject, with particular Uses of common salt . . . .52 reference to the waste and supply or change of matter . . . .69 Certain remedies take a share in trie" vital transformations . . .54 3. Theory of disease . . . .74 Chief qualities of the blood . . .54 4. Theory of respiration . . .77 Modus operandi of organic remedies . 55 All organic poisons contain nitrogen . 56 APPENDIX. Theine identical with caffeine . . 56 Containing the analytical evidence re- Relation of theine and caffeine to bile . 56 ferred to in the sections in which are described the chemical processes of respiration, nutrition, and the metamorphosis of tissues . . .80 Theory of their action . . . .57 Theory of the action of the vegetable alkalies 57 Composition and origin of nervous matter 57 On the conversion of benzoic acid into hippuric acid in the human body, by W.Keller . . . . .101 It is related to that of the vegetable alkalies . . . . . .58 Theory of the action of the latter. . 59 INDEX 103 11 ORGANIC CHEMISTRY APPLIED TO PHYSIOLOGY AND PATHOLOGY. I. In the animal ovum, as well as in the seed of a plant, we recognise a certain remarkable force, the source of growth, or increase in the mass, and of reproduction, or of supply of the matter consumed; a force in a state of rest. By the action of external influences, by impregnation, hy the presence of air and moisture, the condition of static equilibrium of this force is disturbed ; entering into a state of motion or activity, it exhibits itself in the production of a series of forms, which, although occasionally bounded by right lines, are yet widely distinct from geometrical forms, such as we observe in crystallised minerals. This force is called the vital force, or viz vita; vitality. The increase of mass in a plant is determined by the occurrence of a decomposition which takes place in certain parts of the plant under the influence of light and heat. In the vital process, as it goes on in vegetables, it is exclusively inorganic matter which undergoes this decomposition; and if, with the most distinguished mineralogists, we consider atmospherical air and certain other gases as minerals, it may be said that the vital process in vegetables accomplishes the transformation of mineral substances into an organism endued with life; that the mineral becomes part of an organ possessing vital force. The increase of mass in a living plant implies that certain component parts of its nourishment become component parts of the plant; and a comparison of the chemical composition of the plant with that of its nourishment, makes known to us, with positive certainty, which of the component parts of the latter have been assimilated, and which have been rejected. The observations of vegetable physiologists and the researches of chemists have mutually contributed to establish the fact, that the growth and development of vegetables depend on the elimination of oxygen, which is separated from the other component parts of their nourishment. In contradiction to vegetable life, the life of animals exhibits itself in the continual absorption of the oxygen of the air, and its combination with certain component parts of the anima. body. While no part of an organized being can serve as food to vegetables, until, by the processes of putrefaction and decay, it has assumed the form of inorganic matter, the animal organism requires, for its support and development, highly organized atoms. The food of all animals, in all circumstances, consists of parts of organisms. Animals are distinguished from vegetables by the faculty of locomotion, and, in general, by the possession of senses. The existence and activity of these distinguishing faculties depend on certain instruments which are never found in vegetables. Comparative anatomy shows, that the phenomena of motion and sensation depend on certain kinds of apparatus, which have no other relation to each other than this, that they meet in a common centre. The substance of the spinal marrow, the nerves, and the brain, is in its composition, and in its chemical characters, essentially distinct from that of which cellular substance, membranes, muscles, and skin are composed. Every thing in the animal organism, to which the name of motion can be applied, proceeds from the nervous apparatus. The phenomena of motion in vegetables, the circulation of the sap, for example, observed in many of the characeae, and the closing of flowers and leaves, depend on physical and mechanical causes. A plant is destitute of nerves. Heat and light are the remote causes of motion in vegetables; but in animals we recognise in the nervous apparatus a source of power, capable of renewing itself at every moment of their existence. While the assimilation of food in vegetables, and the whole process of their formation, are dependant on certain external influences which produce motion, the development of the animal organism is, to a certain extent, independent of these external influences, just because the animal body can produce within itself that source of motion which is indispensable to the vital process. Assimilation, or the process of formation and growth—in other words, the passage of matter from a state of motion to that of rest ' —goes on in the same way in animals and ANIMAL CHEMISTRY 12 in vegetables. In both, the same cause determines the increase of mass. This constitutes the true vegetative life, which is carried on without consciousness. The activity of vegetative life manifests itself, in vegetables, with the aid of external influences; in animals, by means of influences produced within their organism. Digestion, circulation, - secretion, are no doubt under the influence of the nervous system; hut the force which gives to the germ, the leaf, and the radical fibres of the vegetable the same wonderful properties, is the same as that residing in the secreting membranes and glands of animals, and which enables every animal organ to perform its own proper function. It is only the source of motion that differs in the two great classes of organized beings. While the organs of the vital motions are never wanting in the lowest orders of animals, as in the impregnated germ of the ovum, in which they are developed first of all, we find , in the higher orders of animals, peculiar organs of feeling and sensation, of consciousness and of a higher intellectual existence. Pathology informs us that the true vegetative life is in no way dependant on the presence of this apparatus; that the process of nutrition proceeds in those parts of the body where the nerves of sensation and voluntary motion are paralysed, exactly in the same way as in other parts where these nerves are in the normal condition; and, on the other hand, that the most energetic volition is incapable of exerting any influence on the contractions of the heart, on the motion of the intestines, or on the processes of secretion. The higher phenomena of mental existence cannot, in the present state of science, be referred to their proximate, and still less to their ultimate causes. We only know of them, that they exist; we ascribe them to an immaterial agency, and that, in so far as its manifestations are connected with matter, an agency entirely distinct from the vital force, with which it has nothing in common. It cannot be denied that this peculiar force exercises a certain influence on the activity of vegetative life, just as other immaterial agents, such as Light, Heat, Electricity, and Magnetism do; but this influence is not of a determinative kind, and manifests itself only as an acceleration, a retarding, or a disturbance of the process of vegetative life. In a manner exactly analogous, the vegetative life re-acts on the conscious mental existence. There are thus two forces which are found in activity together; but consciousness and intellect may be absent in animals as they are in living vegetables, without their vitality being otherwise affected than by the want of a peculiar source of increased energy or of disturbance. Except in regard to this, all the vital chemical processes go on precisely in the same way in man and in the lower animals. The efforts of philosophers, constantly renewed, to penetrate the relations of the soul to animal life, have all along retarded the progress of physiology. In this attempt men left the province of philosophical research for that of fancy; physiologists, carried away by imagination, were far from being acquainted with the laws of purely animal life. None of them had a clear conception of the process of development and nutrition, or of the true cause of death. They professed to explain the most obscure psychological phenomena, and yet they were unable to say what fever is, and in what way quinine acts in curing it. For the purpose of investigating' the laws of vital motion in the animal body, only one condition, namely, the knowledge of the apparatus which serves for its production, was ascertained; but the substance of the organs, the changes which food undergoes in the living body, its transformation into portions of organs, and its reconversion into lifeless compounds, the.share which the atmosphere takes in the processes of vitality; all these foundations for future conclusions were still wanting. What has the soul, what have consciousness and intellect to do with the development of the human fetus, or the foetus in a fowl's egg ? not more, surely, than with the development of the seeds of a plant. Let us first endeavour to refer to their ultimate causes those phenomena of life which are not physiological; and let us beware of drawing conclusions before we have a groundwork. We know exactly the mechanism of the eye; but neither anatomy nor chemistry will ever explain how the rays of light act on consciousness, so as to produce vision. Natural science has fixed limits which cannot be passed; and it must always be borne in mind that, with all our discoveries, we shall never know what light, electricity, and magnetism are in their essence, because, even of those things which are material, the human intellect has only conceptions. We can ascertain, however, the laws which regulate their motion and rest, because these are manifested in phenomena. In like manner the laws of vitality, and of all that disturbs, promotes, or alters it, may certainly be discovered, although we shall never learn what life is. Thus the discovery of the laws of gravitation and of the planetary motions led to an entirely new conception of the cause of these phenomena. This conception could not have been formed in all its clearness without a knowledge of phenomena out of which it was evolved; for, considered by itself, gravity, like light to one born blind, is a mere word, devoid of meaning. The modern science of physiology has left the track of Aristotle. To the eternal advantage of science, and to the benefit of mankind, it no longer invents a horror vacui, a quinta essentia, in order to furnish credulous hearers with solutions and explanations CHEMICAL CHANGES. 13 of phenomena, whose true connection with others, whose 'ultimate cause is still unknown. If we assume that all the phenomena exhibited by the organism of plants and animals are to be ascribed to a peculiar cause, different in its manifestations from all other causes which produce motion or change of condition; if, therefore, we regard the vital force as an independent force, then, in the phenomena of organic life, as in all other phenomena ascribed to the action of forces, we have the statics, that is, the state of equilibrium determined by a resistance, and the dynamics, of the vital force. All the parts of the animal body are produced from a peculiar fluid, circulating in its organism, by virtue of an influence residing in every cell, in every organ, or part of an organ. Physiology teaches that all parts of the body were originally blood; or that at least they were brought to the growing organs by means of this fluid. The most ordinary experience farther shows, that at each moment of life, in the animal organism, a continued change of matter, more or less accelerated, is going on; that a part of the structure is transformed into unorganized matter, loses its condition of life, and must be again renewed. Physiology has sufficiently decisive grounds for the opinion, that every motion, every manifestation of force, is the result of a transformation of the structure or of its substance; that every conception, every mental affection, is followed by changes in the chemical nature of the secreted fluids; that every thought, every sensation, is accompanied by a change in the composition of the substance of the brain. In order to keep up the phenomena of life in animals, certain matters are required, parts of organisms, which we call nourishment. In consequence of a series of alterations, they serve either for the increase of the mass (nutrition,) or for the supply of the matter consumed (reproduction,) or, finally, for the production of force. II. If the first condition of animal life be the assimilation of what is commonly called nourishment, the second is a continual absorption of oxygen from the atmosphere. Viewed as an object of scientific research, animal life exhibits itself in a series of phenomena, the connection and recurrence of which are determined by the changes which the food and the oxygen absorbed from the atmosphere undergo in the organism under the influence of the vital force. All vital activity arises from the mutual action of the oxygen of the atmosphere and the elements of the food. In the processes of nutrition and reproduction, we perceive the passage of matter from the state of motion to that of rest (static equilibrium;) under the influence of the nervous system, this matter enters again into a state of motion. The ultimate causes of these different conditions of the vital force are chemical forces. The cause of the state of rest is a resistance, determined by a force of attraction (combination,) which acts between the smallest particles of matter, and is manifested only when these are in actual contact, or at infinitely small distances. To this peculiar kind of attraction we may of course apply different names; but the chemist calls it affinity. The cause of the state of motion is to be found in a series of changes which the food undergoes in the organism, and these are the results of processes of decomposition, to which either the food itself, or the structures formed from it, or parts of organs, are subjected. The distinguishing character of vegetable life is a continued passage of matter from the state of motion to that of static equilibrium. While a plant lives, we cannot perceive any cessation in its growth; no part of an organ in the plant diminishes in size. If decomposition occur, it is the result of assimilation. A plant produces within itself no cause of motion; no part of its structure, from any influence residing in its organism, loses its state of vitality, and is converted into unorganized, amorphous compounds; in a word, no waste occurs in vegetables. Waste, in the animal body, is a change in the state or in the composition of some of its parts, and consequently is the result of chemical actions. The influence of poisons and of remedial agents on the living animal body evidently shows that the chemical decompositions and combinations in the body, which manifest themselves in the phenomena of vitality, may be increased in intensity by chemical forces of analogous character, and retarded or put an end to by those of opposite character ; and that we are enabled to exercise an influence on every part of an organ by means of substances possessing a welldefined chemical action. As, in the closed galvanic circuit, in consequence of certain changes which an inorganic body, a metal, undergoes when placed in contact with an acid, a certain something becomes cognizable by our senses, which we call a current of electricity; so, in the animal body, in consequence of transformations and changes undergone by matter previously constituting a part of the organism, certain phenomena of motion and activity are perceived, and these we call life, or vitality. The electrical current manifests itself in certain phenomena of attraction and repulsion, which it excites in other bodies naturally motionless, and by the phenomena of the formation and decomposition of chemical compounds, which occur every where, when the resistance is not sufficient to arrest the current. It is from this point of view, and from no other, that chemistry ought to contemplate B ANIMAL CHEMISTRY 14 the phenomena of life. Wonders surround us on every side. The formation of a crystal, of an octahedron, is not less incomprehensible than the production of a leaf or of a muscular fibre; and the production of vermilion from mercury and sulphur is as much an enigma as the formation of an eye from the substance of the blood. The first conditions of animal life are nutritious matters and oxygen, introduced into the system. At every moment of his life man is taking oxygen into his system, by means of the organs of respiration; no pause is observable while life continues. The observations of physiologists have shown that the body of an adult man, supplied with sufficient food, has neither increased nor diminished in weight at the end of twenty-four hours; yet the quantity of oxygen taken into the system during this period is very considerable. According to the experiments of Lavoisier, an adult man takes into his system, from the atmosphere, in one year, 746 lbs., according to Menzies, 837 lbs. of oxygen; yet we find his weight, at the beginning and end of the year, either quite the . same, or differing, one way or the other, by at most a few pounds. (1)* What, it may be asked, has become of the enormous weight of oxygen thus introduced, in the course of a year into the human system'? This question may be answered satisfactorily ; no part of this oxygen remains in the system; but it is given out again in the form of a compound of carbon or of hydrogen. The carbon and hydrogen of certain parts of the body have entered into combination with the oxygen introduced through the lungs and through the skin, and have been given out in the forms of carbonic acid gas and the vapour of water. At every moment, with every expiration, certain quantities of its elements separate from the animal organism, after having entered into combination, within the body, with the oxygen of the atmosphere. If we assume, with Lavoisier and Seguin, in order to obtain a foundation for our calculation, that an adult man receives into his system daily (46,037 cubic inches= 15,661 grains, French weight) of oxygen, and that the weight of the whole mass of his blood, of which 80 per cent, is water, is 24 lbs.; it then appears, from the known composition of the blood, that, in order to convert the whole of its carbon and hydrogen into carbonic acid and water, 64,103 grains of oxygen are required. This quantity will be taken into the system of an adult in four days five hours. (2) Whether this oxygen enters into combination with the elements of the blood, or with other parts of the body containing carbon and hydrogen, in either case the conclu- * The Numbers refer to the Appendix. sion is inevitable, that the body of a man, who daily takes into the system 32£ oz. of oxygen, must receive daily in the shape of nourishment, as much carbon and hydrogen as would suffice to supply 24 lbs. of blood with these elements; it being presupposed that the weight of the body remains unchanged, and that it retains its normal condition as to health. This supply is furnished in the food. From the accurate determination of the quantity of carbon daily taken into the system in the food, as well as of that proportion of it which passes out of the body in the faeces and urine, unburned, that is, in some form in which it is not combined with oxygen, it appears that an adult, taking moderate exercise, consumes 13.9 oz. of carbon daily. (3) These 13-A oz. of carbon escape through the skin and lungs as carbonic acid gas. For conversion into carbonic acid gas, oz. of carbon require 37 oz. of oxygen. According to the analyses of Boussingault (Ann. de Ch. et de Ph. LXXI. p. 136) a horse consumes in twenty-four hours 97£ oz. of carbon, a milk cow 69j% oz. The quantities of carbon here mentioned are those given off from the bodies of these animals in the form of carbonic acid; and it appears from them that the horse consumes, in converting carbon into carbonic acid, 13 lbs. oz. in twenty-four hours, and the milk cow 11 lbs. 10| oz. of oxygen in the same time. (4) Since no part of the oxygen taken into the system is again given off in any other form but that of a compound of carbon or hydrogen; since, farther, the carbon and hydrogen given off are replaced by carbon and hydrogen supplied in the food, it is clear that the amount of nourishment required by the animal body must be in a direct ratio to the quantity of oxygen taken into the system. Two animals, which in equal times take up by means of the lungs and skin unequal quantities of oxygen, consume quantities of the same nourishment which are unequal in the same ratio. The consumption of oxygen in equal times may be expressed by the number of respirations; it is clear that, in the same in ¦ dividual, the quantity of nourishment required must vary with the force and number of the respirations. A child, in whom the organs of respiration are naturally very active, requires food oftener than an adult, and bears hunger less easdy. A bird, deprived of food, dies on the third day, while a serpent, with its sluggish respiration, can live without food three months and longer. The number of respirations is smaller in a state of rest than during exercise or work. The quantity of food necessary in both conditions must vary in the same ratio. An excess of food is incompatible with deficiency in respired oxygen, that is, with SOURCE OP ANIMAL HEAT.—RESPIRATION. 15 deficient exercise; just as violent exercise, which implies an increased supply of food, is incompatible with weak digestive organs. In either case the health suffers. * But the quantity of oxygen inspired is also affected by the temperature and density of the atmosphere. The capacity of the chest in an animal is a constant quantity. At every respiration a quantity of air enters, the . volume of which may be considered as uniform; but its weight, and consequently that of the oxygen it contains, is not constant. Air is expanded by heat, and contracted by cold, and therefore equal volumes of hot and cold air contain unequal weights of oxygen. In summer, moreover, atmospherical air contains aqueous vapour, while in winter it is dry; the space occupied by vapour in the warm air is filled up by air itself in winter; that is, it contains, for the same volume, more oxygen in winter than in summer. In summer and in winter, at the pole and at the equator, we respire an equal volume of air; the cold air is warmed during respiration, and acquires the temperature of the body. To introduce into the lungs a given volume of oxygen, less expenditure of force is necessary in winter than in summer ; and for the same expenditure of force, more oxygen is inspired in winter. It is obvious, that in an equal number of respirations we consume more oxygen at the level of the sea than on a mountain. The quantity both of oxygen inspired and of carbonic acid expired, must, therefore, vary with the height of the barometer. The oxygen taken into the system is given out again in the same forms, whether in summer or in winter; hence we expire more carbon in cold weather, and when the barometer is high, than we do in warm weather; and we must consume more or less carbon in our food in the same proportion ; in Sweden more than in Sicily; and in our more temperate climate a full eighth more in winter than in summer. Even when we consume equal weights of food in cold and warm countries, infinite wisdom has so arranged, that the articles of food in different climates .ire most unequal in the proportion of carbon they contain. The fruits on which the natives of the south prefer to feed do not in the fresh state contain more than 12 per cent, of carbon, while the bacon and train oil used by the inhabitants of the arctic regions contain from 66 to 80 per cent, of carbon. It is no difficult matter, in warm climates, to study moderation in eating, and men can bear hunger for a long time under the equator ; but cold and hunger united very soon exhaust the body. The mutual action between the elements of the food and the oxygen conveyed by the circulation of the blood to every part of the body is the source of animal heat. HI. All living creatures, whose existence depends on the absorption of oxygen, pos-, sess within themselves a source of heat independent of surrounding objects. This truth applies to all animals, and extends, besides, to the germination of seeds, to the flowering of plants, and to the maturation of fruits. It is only in those parts of the body to which arterial blood, and with it the oxygen absorbed in respiration, is conveyed, that heat is produced. Hair, wool, or feathers, do not possess an elevated temperature. This high temperature of the animal body, or, as it may be called, disengagement of heat, is uniformly and under all circumstances the result of the combination of a combustible substance with oxygen. In whatever way carbon may Combine with oxygen, the act of combination cannot take place without the disengagement of heat. It is a matter of indifference whether the combination take place rapidly or slowly, at a high or at a low temperature; the amount of heat liberated is a constant quantity. The carbon of the food, which is converted into carbonic acid within the body, must give out exactly as much heat as if it had been directly burnt in the air or in oxygen gas; the only difference is, that the amount of heat produced is diffused over unequal times. In oxygen, the combustion is more rapid, and the heat more intense; in air it is slower, the temperature is not so high, but it continues longer. It is obvious that the amount of heat liberated must increase or diminish with the quantity of oxygen introduced in equal times by respiration. Those animals which respire frequently, and consequently, consume much oxygen, possess a higher temperature than others, which, with a body of equal size to be heated, take into the system less oxygen. The temperature of a child (102°) is higher than that of an adult (99-5°). That of birds (104° to 105-4°) is higher than that of quadrupeds (98 5° to 100*4°) or than that of fishes or amphibia, whose proper temperature is from 27° to 3 - 6° higher than that of the medium in which they live. All animals, strictly speaking are warm-blooded; but in those only which possess lungs is the temperature of the body quite independent of the surrounding medium. (5) The most trustworthy observations prove that in all climates, in the temperate zones as well as at the equator or the poles, the temperature of the body in man, and in what are commonly called warm-blooded animals, is invariably the same; yet how different are the circumstances under which they live! The animal body is a heated mass, which bears the same relation to surrounding objects as any other heated mass. It receives heat when the surrounding objects are hotter, it loses heat when they are colder than itself. We know that the rapidity of cooling in- 16 ANIMAL CHEMISTRY. creases with the difference between the temperature of the heated body and that of the surrounding medium; that is, the colder the surrounding medium the shorter the time required for the cooling of the heated body. How unequal, then, must be the loss of heat in a man at Palermo, where the external temperature is nearly equal to that of the body, and in the polar regions, where the external temperature is from 70° to 90° lower. Yet, notwithstanding this extremely unequal loss of heat, experience has shown that the blood of the inhabitant of the arctic circle has a temperature as high as that of the native of the south, who lives in so different a medium. This fact, when its true significance is perceived, proves that the heat given off to the surrounding medium is restored within the body with great rapidity. This compensation takes place more rapidly in winter than in summer, at the pole than at the equator. Now, in different climates the quantity of oxygen introduced into the system of respiration, as has been already shown, varies according to the temperature of the external air; the quantity of inspired oxygen increases with the loss of heat by external cooling, and the quantity of carbon or hydrogen necessary to combine with this oxygen must be increased in the same ratio. It is evident that the supply of the heat lost by cooling is effected by the mutual action of the elements of the food and the inspired oxygen, which combine together. To make use of a familiar, but not on that account a less just illustration, the animal body acts, in this respect, as a furnace, which we supply with fuel. It signifies nothing what intermediate forms food may assume, what changes it may undergo in the body, the last change is uniformly the conversion of its carbon into carbonic acid, and of its hydrogen into water; the unassimilated nitrogen of the food, along with the unburned or unoxidised carbon, is expelled in the urine or in the solid excrements. In order to keep up in the furnace a constant temperature, we must vary the supply of fuel according to the external temperature, that is, according to the supply of oxygen. In the animal body the food is the fuel; with a proper supply of oxygen we obtain the heat given out during its oxidation or combustion. In winter, when we take exercise in a cold atmosphere, and when consequently, the amount of inspired oxygen increases, the necessity for food containing carbon and hydrogen increases in the same ratio; and by gratifying the appetite thus excited, we obtain the most efficient protection against the most piercing cold. A starving man is soon frozen to death; and every one knows that the animals of prey in the arctic regions far exceed in voracity those of the torrid zone. In cold and temperate climates, the air, which incessantly strives to consume the body, urges man to labourious efforts in order to furnish the means of resistance to its action, while, in hot climates, the necessity of labour to provide food is far less urgent. Our clothing is merely an equivalent for a certain amount of food. The more warmly we are clothed the less urgent becomes the appetite for food, because the loss of heat by cooling, and consequently the amount of heat to be supplied by the food, is diminished. If we were to go naked, like certain savage tribes, or if in hunting or fishing we were exposed to the same degree of cold as the Samoyedes, we should be able with ease to consume 10 lbs. of flesh, and perhaps, a dozen of tallow candles into the bargain, daily, as warmly clad travellers have related with astonishment of these people! We should, then, also be able to take the same quantity of brandy or train oil without bad effects, because the carbon and hydrogen of these substances would only suffice to keep up the equilibrium between the external temperature and that of our bodies. According to the preceding expositions, the quantity of food is regulated by the number of respirations, by the temperature of the air, and by the amount of heat given off to the surrounding medium. No isolated fact, apparently opposed to this statement, can affect the truth of this natural law. Without temporary or permanent injury to health, the Neapolitan cannot take more carbon and hydrogen in the shape of food than he expires as carbonic acid and water; and the Esquimaux cannot expire more carbon and hydrogen than he takes into the system as food, unless in a state of disease or of starvation. Let us examine these states a little more closely. The Englishman in Jamaica sees with regret the disappearance of his appetite, previously a source of frequently recurring enjoyment; and he succeeds by the use of cayenne pepper and the most powerful stimulants, in enabling himself to take as much food as he was accustomed to eat at home. But the whole of the carbon thus introduced into the system is not consumed; the temperature of the air is too high, and the oppressive heat does not allow him to increase the number of respirations by active exercise, and thus to proportion the waste to the amount of food taken; disease of some kind, therefore, ensues. On the other hand, England sends her sick, whose diseased digestive organs have in a greater or less degree lost the power of bringing the food into that state in which it is best adapted for oxidation, and therefore, furnish less resistance to the oxidising agency of the atmosphere than is required in their native climate, to southern regions, where the amount of inspired oxygen is diminished in so great a proportion; and the result, an improvement in the health, is obvious. The diseased organs of diges- EFFECTS OF STARVATION. 17 tion have sufficient power to place the diminished amount of food in equilibrium with the inspired oxygen; in the colder climate, the organs of respiration themselves would have been consumed in furnishing the necessary resistance to the action of the atmospheric oxygen. In our climate, hepatic diseases, or those arising from excess of carbon, prevail in summer; in winter, pulmonic diseases, or those arising from excess of oxygen, are more frequent. The cooling of the body, by whatever cause it may be produced, increases the amount of food necessary. The mere exposure to the open air, in a carriage or on the deck of a ship, by increasing radiation and vaporization, increases the loss of heat, and compels us to eat more than usual. The same is true of those who are accustomed to drink large quantities of cold water, which is given oft' at the temperature of the body, 98-5°. It increases the appetite, and persons of weak constitution find it necessary, by .continued exercise, to supply to the system the oxygen required to restore the heat abstracted by the cold water. Loud and long continued speaking, the crying of infants, moist air, all exert a decided and appreciable influence on the amount of food which is taken. IV. In the foregoing pages, it has been assumed that it is especially carbon and hydrogen which, by combining with oxygen, serve to produce animal heat. In fact, observation proves that the hydrogen of the food plays a not less important part than the carbon. The whole process of respiration appears most clearly developed, when we consider the state of a man, or other animal, totally deprived of food. The first effect of starvation is the disappearance of fat, and this fat cannot be traced in the urine or in the scanty faeces. Its carbon and hydrogen have been given off through the skin and lungs in the form of oxidised products; it is obvious that they have served to support respiration. In the case of a starving man, 32J oz. of oxygen enter the system daily, and are given out again in combination with a part of his body. Currie mentions the case of an individual who was unable to swallow, and whose body lost 100 lbs. in weight during a month; and, according to Martell (Trans. Linn. Soc, vol. xi. p. 411,) a fat pig, overwhelmed in a slip of earth, lived 1G0 days without food, and was found to have diminished in weight, in that time, more than 120 lbs. The whole history of hybernating animals, and the well established facts of the periodical accumulation, in various animals, of fat, which, at other periods, entirely disappears, prove that the oxygen, in the respiratory process, consumes, without exception, all such substances as are capable of entering into combination with it. It combines with 3 whatever is presented to it; and the deficiency of* hydrogen is the only reason why carbonic acid is the chief product; for, at the temperature of the body, the affinity of hydrogen for oxygen far surpasses that of carbon for the same element. We know, in fact, that the graminivora expire a volume of carbonic acid equal to that of the oxygen inspired, while the carnivora, the only class of animals whose food contains fat, inspire more oxygen than is equal in volume to the carbonic acid expired. Exact experiments have shown, that in many cases only half the volume of oxygen is expired in the form of carbonic acid. These observations cannot be gainsaid, and are far more convincing than those arbitrary and artificially produced phenomena, sometimes called experiments; experiments which, made as too often they are, without regard to the necessary and natural conditions, possess no value, and may be entirely dispensed with ; especially when, as in the present case, nature affords the opportunity for observation, and when we make a rational use of that opportunity. In the progress of starvation, however, it is not only the fat which disappears, but also, by degrees, all such of the solids as are capable of being dissolved. In the wasted bodies of those who have suffered starvation, the muscles are shrunk and unnaturally soft, and have lost their contractility ; all those parts of the body which were capable of entering into the state of motion, have served to protect the remainder of the frame from the destructive influence of the atmosphere. Towards the end, the particles of the brain begin to undergo the process of oxidation, and delirium, mania, and death close the scene; that is to say, all resistance to the oxidising power of the atmospheric oxygen ceases, and the chemical process of eremacausis, or decay, commences, in which every part of the body, the bones excepted, enters into combination with oxygen. The time which is required to cause death by starvation depends on the amount of fat in the body, on the degree of exercise, as in labour or exertion of any kind, on the temperature of the air, and finally, on the presence or absence of water. Through the skin and lungs there escapes a certain quantity of water, and as the presence of water is essential to the continuance of the vital motions, its dissipation hastens death. Cases have occurred, in which a full supply of water being accessible to the sufferer, death has not occurred, till after the lapse of twenty days. In one case, life was sustained in this way for the period of sixty days. In all chronic diseases death is produced by the same cause, namely, the chemical action of the atmosphere. When those substances are wanting, whose function in the organism is to support the process of respiration; when the diseased organs are incapable of performing their proper func- b2 18 ANIMAL CHEMISTRY. lion of producing these substances; when they have lost the power of transforming the food into that shape in which it may, by entering into combination with the oxygen of the air, protect the system from its influence, then, the substance of the organs themselves, the fat of the body, the substance of the muscles, the nerves, and the brain, are unavoidably consumed.* The true cause of death in these cases is the respiratory process, that is, the action of the atmosphere. A deficiency of food, and the want of power to convert the food into a part of the organism, are both, equally a want of resistance ; and this is the negative cause of the cessation of the vital process. The flame is extinguished, because the oil is consumed; and it is the oxygen of the air which has consumed it. In many diseases substances are produced which are incapable of assimilation. By the mere deprivation of food, these substances are removed from the body without leaving a trace behind; their elements have entered into combination with the oxygen of the air. From the first moment that the function of the lungs or of the skin is interrupted or disturbed, compounds, rich in carbon, appear in the urine, which acquires a brown colour. Over the whole surface of the body oxygen is absorbed, and combines with all the substances which offer no resistance to. it. In those parts of the body where the access of oxygen is impeded; for example, in the armpits, or in the soles of the feet, peculiar compounds are given out, recognisable by their appearance, or by their odour. These compounds contain much carbon. Respiration is the falling weight, the bent spring, which keeps the clock in motion; the inspirations and expirations are the strokes of the pendulum which regulate it. In our ordinary timepieces, we know with mathematical accuracy the effect produced on their rate of going, by changes in the length of the pendulum, or in the external temperature. Few, however, have a clear conception of the influence of air and temperature on the health of the human body; and yet the research into the conditions necessary to keep it in the nominal state, is not more difficult than in the case of a clock. V. The want of a just conception of force and effect, and of the connection of natural phenomena, has led chemists to attribute a part of the heat generated in the animal body to the action of the nervous system. If this view exclude chemical action, or changes in the arrangement of the elementary particles, as a condition of nervous * For an account of what really takes place in this process, I refer to the considerations on the means by which the change of matter is effected in the body of the carnivora, which will be found farther on. agency, it means nothing else than to derive the presence of motion, the manifestation of a force, from nothing. But no force, no power can come of nothing. No one will seriously deny the share which the nervous apparatus has in the respiratory process; for no change of condition can occur in the body without the nerves; they are essential to all vital motions. Under their influence, the viscera produce those compounds, which, while they protect the organism from the action of the oxygen of the atmosphere, give rise to animal heat; and when the nerves cease to perform their functions, the whole process of the action of oxygen must assume another form. When the pons Varolii is cut through in the dog, or when a stunning blow is inflicted on the back of the head, the animal continues to respire for some time, often more rapidly than in the nominal state; the frequency of the pulse at first rather increases than diminishes, yet the animal cools as rapidly as if sudden death had occurred. Exactly similar observations have been made on the cutting of the spinal chord, and of the par vagum. The respiratory motions continue for a time, but the oxygen does not meet with those substances with which, in the normal state, it would have combined; because the paralysed viscera will no longer furnish them. The singular idea that the nerves produce animal heat, has obviously arisen from the notion that the inspired oxygen combines with carbon, in the blood itself; in which case the temperature of the body, in the above experiments, certainly, ought not to have sunk. But, as we shall afterwards see, there cannot be a more erroneous conception than this. As by the division of the pneumogastric nerves the motion of the stomach and the secretion of the gastric juice are arrested, and an immediate check is thus given to the process of digestion, so the paralysis of the organs of vital motion in the abdominal viscera affects the process of respiration. These processes are most intimately connected; and every disturbance of the nervous system or of the nerves of digestion re-acts visibly on the process of respiration. The observation has been made, that heat is produced by the contraction of the muscles, just as in a piece of caoutchouc, which, when rapidly drawn out, forcibly contracts again, with disengagement of heat. Some have gone so far as to ascribe a part of the animal heat to the mechanical motions of the body, as if these motions could exist without an expenditure of force consumed in producing them; how then, we may ask, is this force produced ? By the combustion of carbon, by the solution of a metal in an acid, by the combination of the two electricities, positive and negative, by the absorption of light, and even by the rubbing of two solid bodies together with a certain degree of rapidity, heat may be produced. GREAT AMOUNT OF ANIMAL HEAT. 19 By a number of causes, in appearance entirely distinct, we can thus produce one and the same effect. In combustion and in the production of galvanic electricity, we have a change of condition in material particles ; when heat is produced by the absorption of light or by friction, we have the conversion of one kind of motion into another, which affects our senses differently. In all such cases we have a something given, which merely takes another form; in all we have a force and its effect. By means of the fire which heats the boiler of a steam engine we can produce every kind of motion, and by certain amount of motion we can produce fire. When we rub a piece of sugar briskly on an iron grater, it undergoes, at the surfaces of contact, the.same change as if exposed to heat; and two pieces of ice, when rubbed together, melt at the point of contact. Let us remember that the most distinguished authorities in physics consider the phenomena of heat as phenomena of motion, because the very conception of the creation of matter, even though imponderable, is absolutely irreconcilable with its production by mechanical causes, such as friction or motion. But, admitting all the influence which electric or magnetic disturbances in the animal body can have on the functions of its organs, still the ultimate cause of all these forces is a change of condition in material particles, which may be expressed by the conversion, within a certain time, of the elements of the food into oxidised products. Such of these elements as do not undergo this process of slow combustion, are given off unburned or incombustible in the exec.rements. Now, it is absolutely impossible that a given amount of carbon or hydrogen, whatever different forms they may assume in the progress of the combustion, can produce more heat than if directly burned into atmospheric air or in oxygen gas. When we kindle a fire under a steam engine, and employ the power obtained to produce heat by friction, it is impossible that the heat thus obtained can ever be greater than that which was required to heat the boiler; and if we use the galvanic current to produce heat, the amount of heat obtained is never in any circumstances, greater than we might have by the combustion of the zinc which has been dissolved in the acid. The contraction of muscles produces heat; but the force necessary for the contraction has manifested itself through the organs of motion, in which it has been excited by chemical changes. The ultimate cause of the heat produced is, therefore, to be found in these chemical changes. By dissolving a metal in an acid, we produce an electrical current; this current, if passed through a wire, converts the wire into a magnet, by means of which, many different effects may be produced. The cause of this phenomena is magnetism; the cause, of the magnetic phenomena is to be found in the electrical current; and the ultimate cause of the electrical current is found to be a chemical change, a chemical action. There are various causes by which force or motion may be produced. A bent spring, a current of air, the fall of water, fire applied to a boiler, the solution of a metal in an acid, —all these different causes of motion may be made to produce the same effect. But in the animal body we recognise as the ultimate cause of all force only one cause, the chemical action which the elements of the food and the oxygen of the air mutually exercises on each other. The only known ultimate cause of vital force, either in animals or in plants, is a chemical process. If this be prevented, the phenomena of life do not manifest themselves, or they cease to be recognisable by our senses. If the chemical action be impeded, the vital phenomena must take new forms. According to the experiments of Despretz, 1 oz. of carbon evolves, during its combustion, as much heat as would raise the temperature of 105 oz. of water at 32° to 167°, that is, by 135 degrees; in all, therefore, 105 times 135°=14207 degrees of heat. Consequently, the 13-9 oz. of carbon which are daily converted into carbonic acid in the body of an adult, evolve 13-9x14207°= 197477-3 degrees of heat. This amount of heat is sufficient to raise the temperature of 1 oz. of water by that number of degrees, or ft;om 32° to 197509-3°; or to cause 136-8 lbs. of water at 32° to boil; or to heat 370 lbs. of water to 98 3° (the temperature of the human body;) or to convert into vapour 24 lbs. of water at 98-3°. If we now assume that the quantity of water vaporized through the skin and lungs in 24 hours amounts to 48 oz. (3 lbs.,) then there will remain, after deducting the necessary amount of heat, 146380-4 degrees of heat, which are dissipated by radiation, by heating the expired air, and in the excrementitious matters. In this calculation, no account has been taken of the heat evolved by the hydrogen of the food, during its conversion into water by oxidation wjiiiin the body. But if we consider that tlW specific heat of the bones, of fat, and of the organs generally, is far less than that of water, and that consequently they require, in order to be heated to 98-3°, much less heat than an equal weight of water, no doubt can be entertained, that when all the concomitant circumstances are included in the calculation, the heat evolved in the process of combustion, to which the food is subjected in the body, is amply sufficient to explain the constant temperature of the body, as well as the evaporation from the skin and lungs. VI. All experiments hitherto made on the quantity of oxygen which an animal consumes in a given time, and also the conclu- 20 ANIMAL CHEMISTRY. sions deduced from them as the origin of animal heat, are destitute of practical value in regard to this question, since we have seen that the quantity of oxygen consumed varies according to the temperature and density of the air, according to the degree of motion, labour, or exercise, to the amount and quality of food, to the comparative warmth of the clothing, and also according to the time within which the food is taken. Prisoners in the Bridewell at Marienschloss (a prison where labour is enforced,) do not consume more than 10-5 oz. of carbon daily; those in the House of Arrest at Giessen, who are deprived of all exercise, consume only 8-5 oz.; (6) and in a family well known to me, consisting of nine individuals, five adults, and four children of different ages, the average daily consumption of carbon for each, is not more than 9 5 oz. of carbon.* We may safely assume, as an approximation, that the quantities of oxygen consumed in these different cases are in the ratio of these numbers; but where the food contains meat, fat, and wine, the proportions are altered by reason of the hydrogen in these kinds of food Avhich is oxidised, and Avhich, in being converted into water, evolves much more heat for equal weights. The attempts to ascertain the amount of heat evolved in an animal for a given consumption of oxygen have been equally unsatisfactory. Animals have been alloAved to respire in close chambers surrounded with cold water; the increase of temperature in the water has been measured by the thermometer, and the quantity of oxygen consumed has been calculated from the analysis of the air before and after the experiment. In experiments thus conducted, it has been found that the animal lost about ¦fo more heat than corresponded to the oxygen consumed; and had the windpipe of the animal been tied, the strange result would have been obtained of a rise in the temperature of the water without any consumption of oxygen. The animal was at the temperature of 98° or 99°, and the water, in the experiments of Despretz, was at 47 - 5°. Such experiments consequently Erove, that when a great difference exists etween the temperature of the animal body, and that of the surrounding medium, and when no motion is allowed, more heat is given off than corresponds to the oxygen consumed. In equal times, with free and unimpeded motion, a much larger quantity of oxygen Avould be consumed without a perceptible increase in the amount of heat lost. The cause of these phenomena is * In this family, the monthly consumption was 151 lbs. of brown bread, 70 lbs. white bread, 132 lbs. meat, 19 lbs. sugar, 159 lbs. butter, 57 maass (about 24 gallons) of milk; the carbon of the potatoes and other vegetables, of the poultry, game, and wine consumed, having been reckoned as equal to that contained in the excrementitious matters, the carbon of the above articles was considered as being converted into carbonic acid. obvious. They appear naturally both in man and animals at certain seasons of the year, and we say in such cases that we are freezing, or experience the sensation of cold. It is plain, that if we were to clothe a man in a metallic dress, and tie up his hands and feet, the loss of heat, for the same consumption of oxygen, would be far greater than if we were to wrap him .up in fur and woollen cloth. Nay, in the latter case, we should see him begin to perspire, and warm water would exude, in drops, through the finest pores of his skin. If to these considerations we add, that decisive experiments are on record, in which animals were made to respire in an unnatural position, as for example, lying on the back, with the limbs tied so as to preclude motion, and that the temperature of their bodies was found to sink in a degree appreciable by the thermometer, we can hardly be at a loss what value we ought to attach to the conclusions drawn from such experiments as those above described. These experiments and the conclusions deduced from them, in short, are incapable of furnishing the smallest support to the opinion that there exists, in the animal body, any other unknown source of heat, besides the mutual chemical action between the elements of the food and the oxygen of the air. The existence of the latter cannot be doubted or denied, and it is amply sufficient to explain all the phenomena. VII. If we designate the production of force, the phenomena of motion in the animal body as nervous life, and the resistance, the condition of static equilibrium, as vegetative life; it is obvious that in all.classes of animals the latter, namely, vegetative life, prevails over the former, nervous life, in the earlier stages of existence. The passage or change of matter from a state of motion to a state of rest appears in an increase of the mass, and in the supply of waste; while the motion itself, or the production of force, appears in the shape of waste of matter. In a young animal, the waste is less than the increase; and the female retains, up to a certain age, this peculiar condition of a more intense vegetative life. This condition does not cease in the female as in the male, Avith the complete development of all the organs of the body. The female in the lower animals, is, at certain seasons, capable of reproduction of the species. The vegetative life in her organism is rendered more intense by certain external conditions, such as temperature, food,&c.; the organism produces more than is wasted, and the result is the capacity of reproduction. In the human species, the female organism is independent of those external causes which increase the intensity of vegetative life. When the organism is fully developed, it is at all times capable of reproduction of the species; and infinite wisdom has given FIBRINE AND ALBUMEN. 21 to the femaie body the power, up to a certain age, of producing all parts of its organization in greater quantity than is required to supply the daily waste. This excess of production can be shown to contain all the elements of a new organism, it is constantly accumulating, and is periodically expelled from the body, until it is expended in reproduction. This periodical discharge ceases when the ovum has been impregnated, and from this time every drop of the superabundant blood goes to produce an organism like that of the mother. Exercise and labour cause a diminution in the quantity of the menstrual discharge; and when it is suppressed in consequence of disease, the vegetative life is manifested in a morbid production of fat. When the equilibrium between the vegetative and nervous life is disturbed in the male, when, as in eunuchs, the intensity of the latter is diminished, the predominance of the former is shown in the same form, in an increased deposit of fat. VIII. If we hold, that increase of mass in the animal body, the development of its organs, and the supply of waste, —that all this is dependent on the blood, that is, on the ingredients of the blood, then only those substances can properly be called nutritious, or considered as food which are capable of conversion into blood. To determine, therefore, what substances are capable of affording nourishment, it is only necessary to ascertain the composition of the food, and to compare it with that of the ingredients of the blood. Two substances require especial consideration as the chief ingredients of the blood"; one of these separates immediately from the blood when withdrawn from the circulation. It is well known that in this case blood coagulates, and separates into a yellowish liquid, the serum of the blood, and a gelatinous mass, which adheres to a rod or stick in soft, elastic fibres, when coagulating blood is briskly stirred. This is the fibrine of the blood, which is identical in all its properties with muscular fibre, when the latter is purified from all foreign matters. The second principal ingredient of the blood is contained in the serum, and gives to this liquid all the properties of the white of eggs, with which it is identical. When heated, it coagulates into a white elastic mass, and the coagulating substance is called albumen. Fibrine and albumen, the chief ingredients of blood, contain, in all, seven chemical elements, among which nitrogen, phosphrus, and sulphur are found. They contain also the earth of bones. The serum retains in solution sea salt and other salts of potash and soda, in which the acids are carbonic, phosphoric, and sulphuric acids. The globules of the blood contain fibrine and albumen, along with a red colouring matter, in which iron is a constant element. Beside these, the blood contains certain fatty bodies in small quantity, which differ from ordinary fats in several of their properties. Chemical analysis has led to the remarkable result, that fibrine and albumen contain the same organic elements united in the same proportion, so that two analyses, the one of fibrine and the other of albumen, do not differ more than two analyses of fibrine or two of albumen respectively do, in the composition of 100 parts. In these two ingredients of blood the particles are arranged in a different order, as is shown by the difference of their external properties; but in chemical composition, in the ultimate proportion of the organic elements, they are identical. This conclusion has lately been beautifully confirmed by a distinguished physiologist (Denis,) who has succeeded in converting fibrine into albumen, that is, in giving it the solubility, and coagulability by heat, which characterize the white of egg. Fibrine and albumen, besides having the same composition, agree also in this, that both dissolve in concentrated muriatic acid, yielding a solution of an intense purple colour. This solution, whether made with fibrine or albumen, has the very same reactions with all substances yet tried. Both albumen and fibrine, in the process of nutrition, are capable of being converted into muscular fibre, and muscular fibre is capable of being reconverted into blood. These facts have long been established by physiologists, and chemistry has merely proved that these metamorphoses can be accomplished under the influence of a certain force, without the aid of a third substance, or of its elements, and without the addition of any foreign element, or the separation of any element previously present in these substances. If we now compare the composition of all organized parts with that of fibrine and albumen, the following relations present themselves : All parts of the animal body which have a decided shape, which forms parts of organs, contain nitrogen. No part of an organ which possesses motion and life is destitute of nitrogen; all of them contain likewise carbon and the elements of water, the latter, however, in no case in the proportion to form water. The chief ingredients of the blood contain nearly 17 per cent, of nitrogen, and no part 6f an organ contains less than 17 per cent, of nitrogen. (7) The most convincing experiments and observations have proved that the animal body is absolutely incapable of producing an elementary body, such as carbon or nitrogen, out of substances which do not contain it; and it obviously follows, that all kinds of food fit for the production either of blood, or of cellular tissue, membranes, skin, hair, muscular fibre, &c, must contain a certain amount of nitrogen, because that element is essential to the composition of 22 ANIMAL CHEMISTRY. the above named organs; because the organs cannot create it from the other elements presented to them; and, finally, because no nitrogen is absorbed from the atmosphere in the vital process. The substance of the brain and nerves contains a large quantity of albumen, and, in addition to this, two peculiar fatty acids, distinguished from other fats by containing phosphorus (phosphoric acid ?) One of these contains nitrogen (Fremy.) Finally, water and common fat are those ingredients of the body which are destitute of nitrogen. Both are amorphus or unorganized, and only so far take part in the vital process as that their presence is required for the due performance of the vital functions. The inorganic constituents of the body are, iron, lime, magnesia, common salt, and the alkalies. IX. The nutritive process in the carnivora is seen in its simplest form. This class of animals lives on the blood and flesh of the graminivora; but this blood and flesh is, in all its properties, identical with their own. Neither chemical nor physiological differences can be discovered. The nutriment of carnivorous animals is derived originally from blood ; in their stomach it becomes dissolved, and capable of reaching all other parts of the body; in its passage it is again converted into blood, and from this blood are reproduced all those parts of their organization which have undergone change or metamorphosis. With the exception of hoofs, hair, feathers, and the earth of bones, every part of the food of carnivorous animals is capable of assimilation. In a chemical sense, therefore, it may be said that a carnivorous animal, in supporting the vital process, consumes itself. That which serves for its nutrition is identical with those parts of its organization which are to be renewed. The process of nutrition in graminivorous animals appear at first sight altogether different. Their digestive organs are less simple, and their food consists of vegetables, the great mass of which contains but little nitrogen. From what substances, it may be asked, is the blood formed, by means of which their organs are developed 1 This question may be answered with certainty. Chemical researches have shown, that all such parts of vegetables as can afford nutri-" ment to animals contain certain constituents which are rich in nitrogen; and the most ordinary experience proves that animals require for their support and nutrition less of these parts of plants in proportion as they abound in the nitrogenized constituents. Animals cannot be fed on matters destitute of these nitrogenized constituents. These important products of vegetation are especially abundant in the seeds of the different kinds of grain, and of pease, beans, and lentils; in the roots and the juices of what are commonly called vegetables. They exist, however, in all plants, without exception, and in every part of plants in larger or smaller quantity. These nitrogenized forms of nutriment in the vegetable kingdom may be reduced to three substances, which are easily distinguished by their external characters. Two of them are soluble in water, the third is insoluble. When the newly expressed juices of vegetables are allowed to stand, a separation takes place in a few minutes. A gelatinous precipitate, commonly of a green tinge, is deposited, and this, when acted on by liquids which remove the colouring matter, leaves a grayish white subtance, well known to druggists as the deposit from vegetable j uices. This is one of the nitrogenized compounds which serves for the nutrition of animals, and has been named vegetable fibrine. The juice of grapes is especially rich in this constituent, but it is most abundant in the seeds of wheat, and of the cerealia. It may be obtained from wheat flour by a mechanical operation, and in a state of tolerable purity; it is then called gluten, but the glutinous property belongs, not to vegetable fibrine, but to a foreign substance, present in small quantity, which is not found in the other cerealia. The method by which it is obtained sufficiently proves that it is insoluble in water j although we cannot doubt that it was originally dissolved in the vegetable juice, from which it afterwards separated, exactly as fibrine does from blood. The second nitrogenized compound remains dissolved in the juice after the separation of the fibrine. It does not separate from the juice at the ordinary temperature, but is instantly coagulated when the liquid containing it is heated to the boiling point. When the clarified juice of nutritious vegetables, such as cauliflower, asparagus, mangel wurzel, or turnips, is made to boil, a coagulum is formed, which it is absolutely impossible to distinguish from the substance which separates as coagulum, when the serum of blood or the white of an egg, diluted with water, are heated to the boiling point. This is vegetable albumen. It is found in the greatest abundance in certain seeds, in nuts, almonds, and others, in which the starch of the graminea? is replaced by oil. The third nitrogenized constituent of the vegetable food of animals isvegetable caseine. It is chiefly found in the seeds of pease, beans, lentils, and similar leguminous seeds. Like vegetable albumen, it is soluble in water, but differs from it in this, that its solution is not coagulated by heat. When the solution is heated or evaporated, a skin forms on its surface, and the addition of an acid causes a coagulum, just as in animal milk. These three nitrogenized compounds, vegetable fibrine, albumen, and caseine, are USES OF THE STARCH, SUGAR, &c. 23 the true nitrogenized constituents of the food of graminivorous animals; all other nitrogenized compounds, occurring in plants, are either rejected by animals, as in the case of the characteristic principles of poisonous and medicinal plants, or else they occur in the food in such very small proportion, that they cannot possibly contribute to the increase of mass in the animal body. The chemical analysis of these three substances has led to the very interesting result that they contain the same organic elements, united in the same proportion by weight; and, what is still more remarkable, that they are identical in composition with the chief constituents of blood, animal fibrine, and albumen. They all three dissolve in concentrated muriatic acid with the same deep purple colour, and even in their physical characters, animal fibrine and albumen are in no respect different from vegetable fibrine and albumen. It is especially to be noticed, that by the phrase, identity of composition we do not here imply mere similarity, but that even in regard to the presence and relative amount of sulphur, phosphorus, and phosphate of lime, no difference can be observed. (8) How beautifully and admirably simple, with the aid of these discoveries, appears the process of nutrition in animals, the formation of their organs, in which vitality chiefly resides ! Those vegetable principles, which in animals are used to form blood, contain the chief constituents of blood, fibrine and albumen, ready formed, as far as regards their composition. All plants, besides, contain a certain quantity of iron, which reappears in the colouring matter of the blood. Vegetable fibrine and animal fibrine, vegetable albumen and animal albumen, hardly differ even in form; if these principles be wanting in the food, the nutrition of the animal is arrested ; and when they are present, the graminivorous animal obtains in its food the very same principles on the presence of which the nutrition of the carnivora entirely depends. Vegetables produce in their organism the blood of all animals, for the carnivora, in consuming the blood and flesh of the graminivora, consume, strictly speaking, only the vegetable principles which have served for the nutrition of the latter. Vegetable fibrine and albumen take the same form in the stomach of the graminivorous animal as animal fibrine and albumen do in that of the carnivorous animal. From what has been said, it follows that the development of the animal organism and its growth are dependent on the reception of certain principles identical with the chief constituents of blood. In this sense we may say that the animal organism gives to blood only its form; that it is incapable of creating blood out of other substances which do not already contain the chief constituents of that fluid. We cannot, indeed, maintain that the animal organism has no power to form other compounds, for we know that it is capable of producing an extensive series of compounds, differing in composition from the chief constituents of blood; but these last, which form the starting point of the series, it cannot produce. The animal organism is a higher kind of vegetable, the development of which begins with those substances, with the production of which the life of an ordinary vegetable ends. As soon as the latter has borne seed, it dies, or a period of its life comes to a termination. In that endless series of compounds, which begins with carbonic acid, ammonia, and water, the sources of the nutrition of vegetables, and includes the most complex constituents of the animal brain, there is no blank, no interruption. The first substance capable of affording nutriment to animals is the last product of the creative energy of vegetables. The substance of cellular tissue and of membranes, of the brain and nerves, these the vegetable cannot produce. The seemingly miraculous in the productive agency of vegetables disappears in a great degree, when we reflect that the production of the constituents of blood cannot appear more surprising than the occurrence of the fat of beef and mutton in cocoa beans, of human fat in olive oil, of the principal ingredient of butter in palm oil, and of horse fat and train oil in certain only seeds. X. While the preceding considerations leave little or no doubt as to the way in which the increase of mass in an animal, that is, its growth, is carried on, there is yet to be resolved a most important question, namely, that of the function performed in the animal system by substances containing no nitrogen, such as sugar, starch, gum, pectine, &c. The most extensive class of animals, the graminivora, cannot live without these substances; their food must contain a certain amount of one or them, and if these compounds are not supplied, death quickly ensues. This important inquiry extends also to the constituents of the food of carnivorous animals in the earliest periods of life; for this food also contains substances which are not necessary for their support in the adult state. The nutrition of the young of carnivora is obviously accomplished by means similar to those by which the graminivora are nourished ; their development is dependant on the supply of a fluid, which the body of the mother secretes in the shape of milk. Milk contains only one nitrogenized constituent, known under the name of caseine ; besides this, its chief ingredients are butter, (fat), and sugar of milk. The blood of the young animal, its muscular fibre, cellular tissue, nervous matter, and bones, must have derived their origin from the nitrogenized constituent of milk, the caseine; for butter and sugar of milk contain no nitrogen. 24 ANIMAL CHEMISTRY. Now, the analysis of caseine has led to the result, which, after the details given in the last section, can hardly excite surprise, that this substance also is identical in composition with the chief constituents of blood, fibrine and albumen. Nay, more, a comparison of its properties with those of vegetable caseine has shown that these two substances are identical in all their properties; insomuch that certain plants, such as peas, beans, and lentils, are capable of producing the same substance which is formed from the blood of the mother, and employed in yielding the blood of the young animal. (9) The young animal, therefore, receives, in the form of caseine, which is distinguished from fibrine and albumen by its great solubility, and by not coagulating when heated, the chief constituent of the mother's blood. To convert caseine into blood no foreign substance is required, and in the conversion of the mother's blood into caseine, no elements of the constituents of the blood have been separated. When chemically examined, caseine is found to contain a much larger proportion of the earth of bones than blood does, and that in a very soluble form, capable of reaching every part of the body. Thus, even in the earliest period of its life, the development of the organs, in which vitality resides, is, in the carnivorous animal, dependant on the supply of a substance, identical in organic composition with the chief constituents of its blood. What, then, is the use of the butter and the sugar of milk? How does it happen that these substances are indispensable to life? Butter and sugar of milk contain no fixed bases, no soda or potash. Sugar of milk has a composition closely allied to that of the other kinds of sugar, of starch, and of gum; all of them contain carbon and the elements of water, the latter precisely in the proportion to form water. There is added, therefore, by means of these compounds, to the nitrogenized constituents of food, a certain amount of carbon, or, as in the case of butter, of carbon and hydrogen; that is, an excess of elements, which cannot possibly be employed in the production of blood, because the nitrogenized substances contained in the food already contain exactly the amount of carbon which is required for the production of fibrine and albumen. The following considerations will show that hardly a doubt can be entertained, that this excess of carbon alone, or of carbon and hydrogen, is expended in the production of animal heat, and serves to protect the organism from the action of the atmospheric oxygen. - XI. In order to obtain a clearer insight into the nature of the nutritive process in both the great classes of animals, let us first consider the changes which the food of the carnivora undergoes in their organism. If we give to an adult serpent, or boa con- stridor, a goat, a rabbit, or a bird, we find that the hair, hoofs, horns, feathers, or bones of these animals, are expelled from the bodyapparently unchanged. They have retained their natural form and aspect, but have become brittle, because of all their component parts they have lost only that one which was capable of solution, namely, the gelatine. Faeces, properly so called, do not occur in serpents any more than in carnivorous birds. We find, moreover, that when the serpent has regained its original weight, every other part of its prey, the flesh, the blood, the brain, and nerves, in short, every thing has disappeared. The only excrement, strictly speaking, is a substance expelled by the urinary passage. When dry, it is pure white, like chalk; it contains much nitrogen, and a small quantity of carbonate and phosphate of lime mixed with the mass. This excrement is urate of ammonia, a chemical compound, in which the nitrogen bears to the carbon the same proportion as in bicarbonate of ammonia. For every equivalent of nitrogen it contains two equivalents of carbon. But muscular fibre, blood membranes, and skin, contain four times as much carbon for the same amount of nitrogen, or eight equivalents to one; and if we add to this the carbon of the fat and nervous substance, it is obvious that the serpent has consumed for every equivalent of nitrogen, much more than eight equivalents of carbon. If now we assume that the urate of ammonia contains all the nitrogen of the animal consumed, then at least six equivalents of carbon, which were in combination with this nitrogen, must have been given out in a different form from the two equivalents which are found in the urate of ammonia. Now we know, with perfect certainty, that this carbon has been given out through the skin and lungs, which could only take place in the form of an oxidized product. The excrements of a buzzard which had been fed with beef, when taken out of the rectum, consisted, according to L. Gmelin and Tiedemann, of urate of ammonia. In like manner, the faices in lions and tigers are scanty and dry, consisting chiefly of bone earth, with mere traces of compounds containing carbon; but their urine contains, not urate of ammonia, but urea, a compound in which carbon and nitrogen are to each other in the same ratio as in neutral carbonate of ammonia. Assuming that their food (flesh, &c.) contains carbon and nitrogen in the ratio of eight equivalents to one, we find these elements in their urine in the ratio of one equivalent to one; a smaller proportion of carbon, therefore, than in serpents, in which respiration is so much less active. The whole of the carbon and hydrogen which the food of these animals contained, beyond the amount which we find in their POOD OF CARNIVORA. 25 excrements, has disappeared, in the process of respiration, as carbonic acid and water. Had the animal food been burned in a furnace, the change produced in it would only have differed in the form of combination assumed by the nitrogen from that which it underwent in the body of the animal. The nitrogen would have appeared, with part of the carbon and hydrogen, as carbonate of ammonia, while the rest of the carbon and hydrogen would have formed carbonic acid and water. The incombustible parts would have taken the form of ashes, and any part of the carbon unconsumed from a deficiency of oxygen would have appeared as soot, or lamp-black. Now the solid excrements are nothing else than the incombustible, or imperfectly burned, parts of the food. In the preceding pages it has been assumed that the elements of the food are converted by the oxygen absorbed in the lungs into oxidized products; the carbon into carbonic acid, the hydrogen into water, and the nitrogen into a compound containing the same elements as carbonate of ammonia. This is only true in appearance; the body, no doubt, after a certain time, acquires its original weight. The amount of carbon, and of the other elements, is not found to be increased—exactly as much carbon, hydrogen, and nitrogen has been given out as was supplied in the food; but nothing is more certain than that the carbon, hydrogen, and nitrogen given out, although equal in amount to what is supplied in that form, do not directly proceed from the food. It would be utterly irrationable to suppose that the necessity of taking food, or the satisfying the appetite, had no other object than the production of urea, uric acid, carbonic acid, and other excrementitious matters—of substances which the system expels, and consequently applies to no useful purpose in the economy. In the adult animal, the food serves to restore the waste of matter; certain parts of its organs have lost the state of vitality, have been expelled from the substance of the organs, and have been metamorphosed into new combinations, which are amorphous and unorganized. The food of the carnivora is at once converted into blood; out of the newly formed blood those parts of organs which have undergone metamorphoses are reproduced. The carbon and nitrogen of the food thus become constituent parts of organs. Exactly as much carbon and nitrogen is supplied to the organs by the blood, that is, ultimately, by the food, as they have lost by the transformations attending the exercise of their functions. What then, it may be asked, becomes of the new compounds produced by the transformations of the organs, of the muscles, of the membranes and cellular tissue of the nerves and brain? These new compounds cannot, owing to 4 their solubility, remain in the situation where they are formed, for a well known force, namely the circulation of the blood, opposes itself to this. By the expansion of the heart, an organ in which two systems of tubes meet, which are ramified in a most minute network of vessels through all parts of the body, there is produced a vacuum, the immediate effect of which is, that all fluids which can penetrate into these vessels are urged with great force towards one side of the heart by the external pressure of the atmosphere. This motion is powerfully assisted by the contraction of the heart, alternating with its expansion, and caused by a force independent of the atmospheric pressure. In a word, the heart is- a forcing pump, which sends arterial blood into all parts of the body; and also a suction pump, by means of which all fluids of whatever kind, as soon as they enter the absorbent vessels which communicate with the veins, are drawn towards the heart. This suction, arising from the vacuum caused by the expansion of the heart, is a purely mechanical act, which extends, as above stated, to fluids of every kind, to saline solutions, poisons, &c. It is obvious, therefore, that by the forcible entrance of arterial blood into the capillary vessels, the fluids contained in these, in other words, the soluble compounds formed by the transformations of organized parts, must be compelled to move towards the heart. These compounds cannot be employed for the reproduction of those tissues from which they are deri ved. They pass through the absorbent and lymphatic vessels into the veins, where their accumulation would speedily put a stop to the nutritive process, were it not that this accumulation is prevented by two contrivances adapted expressly to this purpose, and which may be compared to filtering machines. The venous blood, -before reaching the heart, is made to pass through the liver; the arterial blood, on the other hand, passes through the kidneys; and these organs separate from both all substances incapable of contributing to nutrition. Those new compounds which contain the nitrogen of the transformed organs are collected in the urinary bladder, and being utterly incapable of any further application in the system, are expelled from the body. Those, again, which contain the carbon of the transformed tissues, are collected in the gall bladder in the form of a compound of soda, the bile, which is miscible with water in every proportion, and which, passing into the duodenum, mixes with the chyme. All those parts of the bile which, during the digestive process, do not lose their solubility, return during that process into the circulation in a state of extreme division. The soda of the bile, and those highly carbonized portions which are not precipitated by a weak acid (together making C 26 ANIMAL CHEMISTRY. of the solid contents of the bile,) retain the capacity of resorption by the absorbents of the small and large intestines; nay, this capacity has been directly proved by the administration of enemata containing bile, the whole of the bile disappearing with the injected fluid in the rectum. Thus we know with certainty, that the nitrogenized compounds, produced by the metamorphosis of organized tissues, after being separated from the arterial blood by means of the kidneys, are expelled from the body as utterly incapable of further alteration ; while the compounds, rich in carbon, derived from the same source, return into the system of carnivorous animals. The food of the carnivora is identical with the chief constituents of their bodies, and hence the metamorphoses which their organs undergo must be the same as those which, under the influence of the vital force, take place in the matters which constitute their food. The flesh and blood consumed as food yield their carbon for the support of the respiratory process, while its nitrogen appears as uric acid, ammonia, or urea. But previously to these final changes, the dead flesh and blood become living flesh and blood, and it is, strictly speaking, the carbon of the compounds formed in the metamorphoses of living tissues that serves for the production of animal heat. The food of the carnivora is converted into blood, which is destined for the reproduction of organized tissues; and by means of the circulation a current of oxygen is conveyed to every part of the body. The globules of the blood, which in themselves can be shown to take no share in the nutritive process, serve to transport the oxygen, which they give up in their passage through the capillary vessels. Here the current of oxygen meets with the compounds produced by the transformation of the tissues, and combines with their carbon to form carbonic acid, with their hydrogen to form water. Every portion of these substances which escapes this process of oxidation is sent back into the circulation in the form of the bile, which by degrees completely disappears. In the carnivora the bile contains the carbon of the metamorphosed tissues; this carbon disappears in the animal body, and the bile likewise disappears in the vital process. Its carbon and hydrogen are given out through the skin and lungs as carbonic acid and water; and hence it is obvious that the elements of the bile serve for respiration and for the production of animal heat. Every part of the food of carnivorous animals is capable of forming blood; their excrements, excluding the urine, contain only inorganic substances, such as phosphate of lime; and the small quantity of organic matter which is found mixed with these is derived from excretions, the use of which is to promote their passage through the intes- tines, such as mucus. These excrements contain no bile and no soda; for water extracts from them no trace of any substance resembling bile, and yet bile is very soluble in water, and mixes with it in every proportion. Physiologists can entertain no doubt as to the origin of the constituent parts of the urine and of the bile. When, from the deprivation of food, the stomach contracts itself so as to resemble a portion of intestine, the gall-bladder, for want of the motion which the full stomach gives to it, cannot pour out the bile it contains; hence in animals starved to death we find the gall-bladder distended and full. The secretion of bile and urine goes on during the winter sleep of hybernating animals; and we knoAV that the urine of dogs, fed for three weeks exclusively on pure sugar, contains as much of the most highly nitrogenized constituent, urea, as in the normal condition. (Marchaud. Erdmaun's Journal fur praktische Chemie, XIV. p. 495.) Differences in the quantity of urea secreted in these and similar experiments are explained by the condition of the animal in regard to the amount of the natural motions permitted. Every motion increases the amount of organized tissue which undergoes metamorphosis. Thus after a walk, the secretion of urine in man is invariably increased. The urine of the mammalia, of birds, and of amphibia, contains uric acid or urea; and the excrements of the mollusca, and of insects, as of cantharides and of the butterfly of the silkworm, contain urate of ammonia. This constant occurrence of one or two nitrogenized compounds in the excretions of animals, while so great a difference exists in their food, clearly proves that these compounds proceed from one and the same source. As little doubt can be entertained in regard to the function of the bile in the vital process. When we consider, that the acetate of potash, given in enema, or simply as a bath for the feet, renders the urine strongly alkaline (Rehberger in Tiedemann's Zeitschrift fur Physiologie, ii. 149,) and that the change which the acetic acid here undergoes cannot be conceived without the addition of oxygen, it is obvious, that the soluble constituents of the bile, prone to change in a high degree as we know them to be, and which, as already stated, cannot be employed in the production of blood, must, when returned through the intestines into the circulation, in like manner yield to the influence of the oxygen which they meet. The bile is a compound of soda, the elements of which, with the exception of the soda, disappears in the body of a carnivorous animal. In the opinion of many of the most distinguished physiologists, the bile is intended solely to be excreted; and nothing is more certain, than that a substance containing so very small a proportion of nitrogen can USES OF URINE AND BILE. 27 have no share in the process of nutrition or reproduction of organized tissue. But quantitative physiology must at once and decidedly reject the opinion, that the bile serves no purpose in the economy, and is incapable of further change. No part of any organized structure contains soda; only in the serum of the blood, in the fat of the brain, and in the bile, do we meet with that alkali. When the compounds of soda in the blood are converted into muscular fibre, membrane, or cellular tissue, the soda they contain must enter into new combinations. The blood which is transformed into organized tissue gives up its soda to the compounds formed by the metamorphoses of the previously existing tissues. In the bile we find one of those compounds of soda. Were the bile intended merely for excretion, we should find it, more or less altered, and also the soda it contains, in the solid excrements. But, with the exception of common salt, and of sulphate of soda, which occur in all the animal fluids, only mere traces of soda are to be found in the faeces. The -soda of the bile, therefore, at all events, must have returned from the intestinal canal into the organism, and the same must be true of the organic matters which were in combination with it. According to the observations of physiologists, a man secretes daily from 17 to 24 oz. of bile ; a large dog, 36 oz.; a horse 37 lbs. t Burdach's Physiologie, v. p. 260.) But the faeces of a man do not on an average weigh more than 5 J oz.; and those of a horse 28£ lbs., of which 21 lbs. are water, and 1\ lbs. dry faeces. (Boussingault.) The latter yield to alcohol only uVth part of their weight of soluble matter. If we assume the bile to contain 90 per cent, of water, a horse secretes daily 592 oz. of bile, containing 59 - 2 oz. of solid matter ; while 1\ lbs. or 120 oz. of dried excrement yield only 6 oz. of matter soluble in alcohol, which might possibly be bile. But this matter is not bile; "when the alcohol is dissipated by evaporation, there remains a soft, unctuous mass, altogether insoluble in water, and which, when incinerated, leaves no alkaline ashes, no soda. (10.) During the digestive process, therefore, the soda of the bile, and, along with it, all the soluble parts of that fluid, are returned into the circulation. This soda re-appears in the newly-formed blood, and, finally, we find it in the urine in the form of phosphate, carbonate, and hippurate of soda. Berzelius found in 1,000 parts of fresh human faeces only nine parts of substance similar to bile; 5 ounces, therefore, would contain only 21 grains of dried bile, equivalent to 219 grains of fresh bile. But a man secretes daily from 9,640 to 11,520 grains of fluid bile, that is, from 45 to 56 times as much as can be detected in the matters discharged by the intestinal canal. Whatever opinion we may entertain of the accuracy of the physiological experiments, in regard to the quantity of bile secreted by the different classes of animals; thus much is certain, that even the maximum of supposed secretion, in man and in the horse, does not contain as much carbon as is given out in respiration. With all the fat which is mixed with it, or enters into its composition, dried bile does not contain more than 69 per cent, of carbon. Consequently, if a horse secretes 57 lbs. of bile, this quantity will contain only 40 ounces of carbon. But the horse expires daily nearly twice as much in the form of carbonic acid. A precisely similar proportion holds good in man. Along with the matter destined for the formation or reproduction of organs, the circulation conveys oxygen to all parts of the body. Now, into whatever combination the oxygen may enter in the blood, it must be held as certain, that such of the constituents of blood as are employed for reproduction, are not materially altered by it. In muscular fibre we find fibrine, with all the properties it had in venous blood; the albumen in the blood does not combine with oxygen. The oxygen may possibly serve to convert into the gaseous state some unknown constituent of the blood; but those well-known constituents, which are employed in reproduction, cannot be destined to support the respiratory process; none of their properties can justify such an opinion. Without attempting in this place to exhaust the whole question of the share taken by the bile in the vital operations, it follows, as has been observed, from the simple comparison of those part* of the food of the carnivora which are capable of assimilation, with the ultimate products into which it is converted, that all the carbon of the food, except that portion which is found in the urine, is given out as carbonic acid. But this carbon was ultimately derived from the substance of the metamorphosed tissues; and this being admitted, the question of the necessity of substances containing much carbon and no nitrogen in the food of the young of the carnivora, and in that of the graminivora, is resolved in a strikingly simple manner. XII. It cannot be disputed that in an adult carnivorous animal, which neither gains nor loses weight perceptibly from day to day, its nourishment, the waste of organized tissue, and its consumption of oxygen, stand to each other in a well-defined and fixed relation. The carbon of the carbonic acid given off, with that of the urine; the nitrogen of the urine, and the hydrogen given off as ammonia and water; these elements, taken together, must be exactly equal in weight to the carbon, nitrogen, and hydrogen of the metamorphosed tissues, and since these last are exactly replaced by the food, to the carbon, nitrogen, and hydrogen of the food. Were this not the case, the weight of the 28 ANIMAL CHEMISTRY. animal could not possibly remain unchanged. But, in the young of the carnivora, the weight does not remain unchanged; on the contrary, it increases from day to day by an appreciable quantity. This fact presupposes, that the assimilative process in the young animal is more energetic, more intense, than the process of transformation in the existing tissues. If both processes were equally active, the weight of the body could not increase; and were the waste by transformation greater, the weight of the body would decrease. Now, the circulation in the young animal is not weaker, but, on the contrary, more rapid; the respirations are more frequent; and, for equal bulks, the consumption of oxygen must be greater rather than smaller in the young than in the adult animal. But, since the metamorphosis of organized parts goes on more slowly, there would ensue a deficiency of those substances, the carbon and hydrogen of which are adapted for combination with oxygen ; because, in the carnivora it is the new compounds, produced by the metamorphosis of organized parts, which nature has destined to furnish the necessary resistance to the action of the oxygen, and to produce animal heat. What is wanting for these purposes an infinite wisdom has supplied to the young animal in its natural food. The carbon and hydrogen of butter, and the carbon of the sugar of milk, no part of either of which can yield blood, fibrine, or albumen, are destined for the support of the respiratory process, at an age when a greater resistance is opposed to the metamorphosis of existing organisms; or, in other words, to the production of compounds, which in the adult state are produced in quantity amply sufficient for the purpose of respiration. The young animal receives the constituents of its blood in the caseine of the milk. A metamorphosis of existing organs goes on, for bile and urine are secreted; the matter of the metamorphosed parts is given off in the form of urine, of carbonic acid, and of water; but the butter and sugar of milk also disappear; they cannot be detected in the fasces. The butter and sugar of milk are given out in the form of carbonic acid and water, and their conversion into oxidized products furnishes the clearest proof that far more oxygen is absorbed than is required to convert the carbon and hydrogen of the metamorphosed tissues into carbonic acid and water. The change and metamorphosis of organized tissues going on in the vital process in the young animal, consequently yield, in a given time, much less carbon and hydrogen in the form adapted for the respiratory process than corresponds to the oxygen taken up in the lungs. The substance of its organized parts would undergo a more rapid consump- tion, and would necessarily yield to the action of the oxygen, were not the deficiency of carbon and hydrogen supplied from another source. The continued increase of mass, or growth, and the free and unimpeded developement of the organs of the young animal, are dependent on the presence of foreign substances, which, in the nutritive process, have no other function than to protect the newly-formed organs from the action of the oxygen. It is the elements of these substances which unite with the oxygen; the organs themselves could not do so without being consumed; that is, growth, or increase of mass in the body, the consumption of oxygen remaining the same, would be utterly impossible. The preceding considerations leave no doubt as to the purpose for which Nature has added to the food of the young of carnivorous mammalia substances devoid of nitrogen, which their organism cannot employ for nutrition, strictly so called, that is, for the production of blood; substances which may be entirely dispensed with in their nourishment in the adult state. In the young of carnivorous birds, the want of all motion is an obvious cause of diminished waste in the organized parts; hence, milk is not provided for them. The nutritive process in the carnivora thus presents itself in two distinct forms; one of which we again meet with in the graminivora. XIII. In the class of graminivorous animals, we observe, that during their whole life, their existence depends on the supply of substances having a composition identical with that of sugar of milk, or closely resembling it. Every thing that they consume as food contains a certain quantity of starch, or gum, or sugar, mixed with other matters. The most abundant and widely-extended of the substances of this class is amylon or starch; it occurs in roots, seeds, and stalks, and even in wood, deposited in the form of roundish or oval globules, which differ from each other in size alone, being identical in chemical composition. (11.) In the same plant, in the pea, for example, we find starch, the globules of which differ in size. Those in the expressed juice of the stalks have a diameter of from to of an inch, while those in the seeds are three or four times larger. The globules in arrowroot and in potato starch are distinguished by their large size; those of rice and of wheat are remarkably small. It is well known that starch may be converted into sugar by very different means. This change occurs in the process of germination, as in malting, and it is easily accomplished by the action of acids. The metamorphosis of starch into sugar depends simply, as is proved by analysis, on the addition of the elements of water. (12.) All the carbon of the starch is found in the sugar: none of its elements have been NUTRITION OF THE GRAMINIVORA. 29 separated, and, except the elements of water, no foreign element has been added to it in this transformation. force than the elements of the different kinds of sugar. There is, however, a certain relation between gum and sugar of milk, since both of them, when treated with nitric acid, yield the same oxidized product, namely mucic acid, which cannot, under the same circumstances, be formed from any of the other kinds of sugar. In order to show more distinctly the similarity of composition in these different substances, which perform so important a part in the nutritive process of the graminivora, let us represent one equivalent of carbon by C (=75-8,) and one equivalent of water by aqua (=112*4,) we shall then have for the composition of these substances the following expressions: In many, especially in pulpy fruits, which when unripe are sour and rough to the taste, but when ripe are sweet, as, for example, in apples and pears, the sugar is produced from the starch which the unripe fruit contains. If we rub unripe apples or pears on a grater to a pulp, and wash this with cold water, on a fine sieve, the turpid liquid which passes through deposits a very fine flour of starch, of which not even a trace can be detected in the ripe fruit. Many varieties become sweet while yet on the tree ; these are the summer or early apples and pears. Others, again, become sweet only after having been kept for a certain period after gathering. The after-ripening, as this change is called, is a purely chemical process, entirely independent of the vitality of the plant. When vegetation ceases, the fruit is capable of reproducing the species, that is,"the kernel, stone, or true seed is fully ripe, but the fleshy covering from this period is subjected to the action of the atmosphere. Like all substances in a state of eremacausis, or decay, it absorbs oxygen, and gives off a certain quantity of carbonic acid gas. In the same way as the starch in putrefying paste, in which it is in contact with decaying gluten, is converted into sugar, the starch in the above-named fruits, in a state of decay, or eremacausis, is transformed into grape sugar. The more starch the unripe fruit contains, the sweeter does it become when ripe. A close connexion thus exists between sugar and starch. By means of a variety of chemical actions, which exert no other influence on the elements of starch than that of changing the direction of their mutual attraction, we can convert starch into sugar, but it is always grape sugar. Sugar of milk in many respects resembles starch; (13) it is, by itself, incapable of the vinous fermentation, but it acquires the property of resolving itself into alcohol and carbonic acid when it is exposed to heat in contact with a substance in the state of fermentation (such as putrefying cheese in milk.) In this case, it is first converted into grape sugar; and it undergoes the same transformation, when it is kept in contact with acids—with sulphuric acid, for example—at the ordinary temperature. Gum has the same composition in 100 parts as cane sugar. (14.) It is distinguished from the different varieties of sugar by its not possessing the property of being resolved into alcohol and carbonic acid by the process of putrefaction. When placed in contact with fermenting substances, it undergoes no appreciable change, whence we may conclude, with some degree of probability, that its elements, in the peculiar arrangement according to which they are Starch . . . =12 C+10 aqua. Cane sugar . =12 C+10 aqua+1 aqua. Gum . . . =12 C+10 aqua+1 aqua. Sugar of milk . =12 C+10 aqua+2 aqua. Grape sugar . =12 C+10 aqua+4 aqua. For the same number of equivalents of carbon, starch contains 10 equivalents, cane sugar and gum 11 equivalents, sugar of milk 12 equivalents, and grape-sugar 14 equivalents of water, or the elements of water. XIV. In these different substances, some one of which is never wanting in the food of the graminivora, there is added to the nitrogenized constituents of this food, to the vegetable albumen, fibrine, and caseine, from which their blood is formed, strictly speaking, only a certain excess of carbon, which the animal organism cannot possibly employ to produce fibrine or albumen, because the nitrogenized constituents of the food already contain the carbon necessary for the production of blood, and because the blood in the body of the carnivora is formed without the aid of this excess of carbon. The function formed in the vital process of the graminivora by these substances (sugar, gum, &c.) is indicated in a very clear and convincing manner, when we take into consideration the very small relative amount of the carbon which these animals consume in the nitrogenized constituents of their food, which bears no proportion whatever to the oxygen absorbed through the skin and lungs. A horse, for example, can be kept in a perfectly good condition, if he obtains as food 15 lbs. of hay and 4$ lbs. of oats daily. If we now calculate the whole amount of nitrogen in these matters, as ascertained by analysis (1-5 per cent, in the hay, 2-2 per cent, in the oats,) (15) in the form of blood, that is, as fibrine and albumen, with the due proportion of water in blood, (80 per cent.,) the horse receives daily no more than 4$ oz. of nitrogen, corresponding to about 8 lbs. of blood. But along with this nitrogen, that is, combined with it in the form of fibrine or albumen, the animal receives only about 14 J oz. of carbon. Only about 8 oz. of this can be employed to support respiration, for with united, are held together with a stronger [ the nitrogen expelled in the urine there are 30 ANIMAL CHEMISTRY. combined, in the form of urea, 3 oz., and in the form of hippuric acid, 3£ oz. of carbon. Without going further into the calculation it will readily be admitted, that the volume of air inspired and expired by a horse, the quantity of oxygen consumed, and, as a necessary consequence, the amount of carbonic acid given out by the animal, is much greater than in the respiratory process in man. But an adult man consumes daily about 14 oz. of carbon, and the determination of Boussingault, according to which a horse expires 79 oz. daily, cannot be very far from the truth. In the nitrogenized constituents of -his food, therefore, the horse receives rather less than the fifth part of the carbon which his organism requires for the support of the respiratory process; and we see that the wisdom of the Creator has added to his food the fths which are wanting, in various forms, as, starch, sugar, &c. with which the animal must be supplied, or his organism will be destroyed by the action of the oxygen. It is obvious, that in the system of the graminivora, whose food contains so small a proportion, relatively, of the constituents of blood, the process of metamorphosis in existing tissues, and consequently their restoration or reproduction, must go on far less rapidly than in the carnivora. Were this not the case, a vegetation a thousand times more luxuriant than the actual one would not suffice for their nourishment. Sugar, gum, and starch would no longer be necessary to support life in these animals, because, in that case, the products of the waste, or metamorphosis of the organized tissues, would contain enough of carbon to support the respiratory process. Man, when confined to animal food, requires for his support and nourishment extensive sources of food, even more widely extended than the lion and tiger, because, when he has the opportunity, he kills without eating. A nation of hunters, on a limited space, is utterly incapable of increasing its numbers beyond a certain point, which is soon attained. The carbon necessary for respiration must be obtained from the animals, of which only a limited number can live on the space supposed. These animals collect from the plants the constituents of their organs and of their blood, and yield them, in turn, to the savages who live by the chase alone. They, again, receive this food unaccompanied by those compounds, destitute of nitrogen, which, during the life of the animals, served to support the respiratory process. In such men, confined to an animal diet, it is the carbon of the flesh and of the blood which must take the place of starch and sugar. But 15 lbs. of flesh contain not more carbon than 4 lbs. of starch, (16) and while the savage with one animal and an equal weight of starch could maintain life and health for a certain number of days, he would be com- pelled, if confined to flesh, in order to procure the carbon necessary for respiration, during the same time, to consume five such animals. It is easy to see, from these considerations, how close the connexion is between agriculture and the multiplication of the human species. The cultivation of our crops has ultimately no other object than the production of a maximum of those substances which are adapted for assimilation and respiration, in the smallest possible space. Grain and other nutritious vegetables yield us, not only in starch, sugar, and gum, the carbon which protects our organs from the action of oxygen, and produces in the organism the heat which is essential to life, but also in the form of vegetable fibrine, albumen, and caseine, our blood, from which the other parts of our body are developed. Man, when confined to animal food, respires, like the carnivora, at the expense of the matters produced by the metamorphosis of organized tissues; and, just as the lion, tiger, hyaena, in the cages of a menagerie, are compelled to accelerate the waste of the organized tissues by incessant motion, in order to furnish the matter necessary for respiration, so the savage, for the very same object, is forced to make the most laborious exertions and go through a vast amount of muscular exercise. He is compelled to consume force merely in order to supply matter for respiration. Cultivation is the economy of force. Science teaches us the simplest means of obtaining the greatest effect with the smallest expenditure of power, and with given means to produce a maximum of force. The unprofitable exertion of power, the waste of force in agriculture, in other branches of industry, in science, or in social economy, is characteristic of the savage state, or of the want of cultivation. XV. A comparison of the urine of the carnivora with that of the graminivora shows very clearly, that the process of metamorphosis in the tissues is different, both in form and in rapidity, in the two classes of animals. The urine of carnivorous animals is acid, and contains alkaline bases united with uric, phosphoric, and sulphuric acids. We know perfectly the source of the two latter acids. All the tissues, with the exception of cellular tissue and membrane, contain phosphoric acid and sulphur, which latter element is converted into sulphuric acid by the oxygen of the arterial blood. In the various fluids of the body there are only traces of phosphates or sulphates, except in the urine, where both are found in abundance. It is plain that they are derived from the metamorphosed tissues; they enter into the venous blood in the form of soluble salts, and are separated from it in its passage through the kidneys. The urine of the graminivora is alkaline; it contains alkaline carbonates in abundance, ORIGIN OF FAT IN ANIMALS. 31 and so small a portion of alkaline phosphates as to have been overlooked by most observers. The deficiency or absence of alkaline phosphates in the urine of the graminivora, obviously indicates the slowness with which the tissues in this class of animals are metamorphosed ; for if we assume that a horse consumes a quantity of vegetable fibrine and albumen corresponding to the amount of nitrogen in his daily food (about 4£ oz.,) and that the quantity of tissue metamorphosed is equal to that newly formed, then the quantity of phosphoric acid which on these suppositions would exist in the urine is not so small as not to be easily detected by analysis in the daily secretion of urine (3 lbs. according to Boussingault;) for it would amount to 0.8 per cent. But, as above stated, most observers have been unable to detect phosphoric acid in the urine of the horse. Hence it is obvious that the phosphoric acid which in consequence of the metamorphosis of tissues is produced in the fortn of soluble alkaline phosphates, must re-enter the circulation in this class of animals. It is there employed in forming brain and nervous matter, to which it is essential, and also, no doubt, in contributing to the supply of the earthy part of the bones. It is probable, however, that the greater part of the earth of bones is obtained by the direct assimilation of phosphate of lime, while the soluble phosphates are better adapted for the production of nervous matter. In the graminivora, therefore, whose food contains so small a proportion of phos{)horus or of phosphates, the organism colects all the soluble phosphates produced by the metamorphosis of tissues, and employs them for the developement of the bones and of the phosphorised constituents of the brain ; the organs of excretion do not separate these salts from the blood. The phosphoric acid, which, by the change of matter, is separated in the uncombined state, is not expelled from the body as phosphate of soda; but we find it in the solid excrements in the form of insoluble earthy phosphates. XVT. If we now compare the capacity for increase of mass, the assimilative power in the graminivora and carnivora, the commonest observations indicate a very marked difference. A spider, which sucks with extreme voracity the blood of the first fly, is not disturbed or excited by a second or third. A cat will eat the first, and perhaps the second mouse presented to her, but even if she kills a third, she does not devour it. Exactly similar observations have been made in regard to lions and tigers, which only devour their prey when urged by hunger. Carnivorous animals, indeed, require less food for their mere support, because their skin is destitute of perspiratory pores, and because they consequently lose, for equal bulks, much less heat than graminivorous ani- mals, which are compelled to restore the lost heat by means of food adapted for respiration. How differeut is the energy and intensity of vegetative life in the graminivora. A cow, or a sheep, in the meadow, eats, almost without interruption, as long as the sun is above the horizon. Their system possesses the power of converting into organized tissues all the food they devour beyond the quantity required for merely supplying the waste of their bodies. All the excess of blood produced is converted into cellular and muscular tissue; the graminivorous animal becomes fleshy and plump, while the flesh of the carnivorous animal is always tough and sinewy. If we consider the case of a stag, a roedeer, or a hare, animals which consume the same food as cattle and sheep, it is evident that, when well supplied with food, their growth in size, their fattening, must depend on the quantity of vegetable albumen, fibrine, or caseine, which they consume. With free and unimpeded motion and exercise, enough of oxygen is absorbed to consume the carbon of the gum, sugar, starch, and of all similar soluble . constituents of their food. But all this is very differently arranged in our domestic animals, when with an abundant supply of food, we check the processes of cooling and exhalation, as we do when we feed them in stables, where free motion is impossible. The stall-fed animal eats, and reposes merely for digestion. It devours in the shape of nitrogenized compounds far more food than is required for reproduction, or the supply of waste alone; and at the same time it eats far more of substances devoid of nitrogen than is necessary merely to support respiration and to keep up animal heat. Want of exercise and diminished cooling are equivalent to a deficient supply of oxygen; for when these circumstances occur, the animal absorbs much less oxygen than is required to convert into carbonic acid the carbon of the substances destined for respiration. Only a small part of the excess of carbon thus occasioned is expelled from the body in the horse and ox, in the form of hippuric acid; and all the remainder is employed in the production of a substance which, in the normal state, only occurs in small quantity as a constituent of the nerves and brain. This substance is fat. In the normal condition, as to exercise and labour, the urine of the horse and ox contains benzoic acid (with 14 equivalents of carbon;) but as soon as the animal is kept quiet in the stable, the urine contains hippuric acid, (with 18 equivalents of carbon.) The flesh of wild animals is devoid of fat;, while that of stall-fed animals is covered with that substance. When the fattened animal is allowed to move more 32 ANIMAL CHEMISTRY. freely in the air, or compelled to draw heavy burdens, the fat again disappears. It is evident, therefore, that the formation of fat in the animal body is the result of a want of due proportion between the food taken into the stomach and the oxygen absorbed by the lungs and the skin, A pig, when fed with highly nitrogenized food, becomes full of flesh; when fed with potatoes (starch) it acquires little flesh, but a thick layer of fat. The milk of a cow, when stall-fed, is very rich in butter, but in the meadow is found to contain more caseine, and in the same proportion less butter and sugar of milk. In the human female, beer, and farinaceous diet increase the proportion of butter in the milk; an animal diet yields less milk, but it is richer in caseine. If we reflect, that in the entire class of carnivora, the food of which contains no substance devoid of nitrogen except fat, the production of fat in the body is utterly insignificant; that even in these animals, as in dogs and cats, it increases as soon as they live on a mixed diet; and that we can increase the formation of fat in other domestic animals at pleasure, but only by means of food containing no nitrogen; we can hardly entertain a doubt that such food, in its various forms of starch, sugar, &c, is closely connected with the production of fat. In the natural course of scientific research, we draw conclusions from the food in regard to the tissues or substances formed from it; from the nitrogenized constituents of plants we draw certain inferences as to the nitrogenized constituents of the blood; and it is quite in accordance with this, the natural method, that we should seek to establish the relations of those parts of our food which are devoid of nitrogen and those parts of the body which contain none of that element. It is impossible to overlook the very intimate connexion between them. If we compare the composition of sugar of milk, of starch, and of the other varieties of sugar, with that of mutton and beef suet and of human fat, we find that in all of them the proportion of carbon to hydrogen is the same, and that they only differ in that of oxygen. According to the analyses of Chevreul, mutton fat, human fat, and hogs' lard, contain 29 per cent, of carbon to 11.1, 11.4, and 11.7 per cent, of hydrogen respectively. (16) Starch contains 44.91 carbon to 6.11 hydrogen. Gum and sugar 42.58 carbon to 6.37 hydrogen. (17) It is obvious that these numbers, representing the relative proportions of carbon and hydrogen in starch, gum, and sugar, are in the same ratio as the carbon and hydrogen in the different kinds of fat; {pr 44-91 : 611 =79 : 10-99 42-58 : 6-37 = 79 : 11-80 From which it follows, that sugar, starch, and gum, by the mere separation of a part of their oxygen, may pass into fat, or at least into a substance having exactly the composition of fat. If from the formula of starch, C ,2 H 10 O 10 , we take 9 equivalents of oxygen, there will remain in 100 parts— C 12 - - - 79 4 H'° - - - 10-8 O - - - 9-8 The empirical formula of fat which comes nearest to this is C n H ,0 O, which gives in 100 parts— C» - - - 78-9 H 10 - 1 - 11-6 O ... 95 According to this formula, an equivalent of starch, in order to be changed into fat would lose 1 equivalent of carbonic acid, CO 2 , and 7 equivalents of oxygen. Now the composition of all saponifiable fatty bodies agrees very closely with one or other of these two formulae. If from 3 equivalents of sugar of milk, 3C 12 H 12 0 12 =C 36 H 3 «0 M , we take away four equivalents of water and 31 of oxygen, there will remain a formula which accurately represents the composition of cholesterine, the fat of bile. (18.) Whatever views we may entertain regarding the origin of the fatty constituents of the body, this much at least is undeniable, that the herbs and roots consumed by the cow contain no butter; that in hay or the other fodder of oxen no beef suet exists; that no hogs' lard can be found in the potato refuse given to swine; and that the food of geese or fowls contains no goose fat or capon fat. The masses of fat found in the bodies of these animals are formed in their organism; and when the full value of this fact is recognised, it entitles us to conclude that a certain quantity of oxygen, in some form or other, separates from the constituents of their food; for without such a separation of oxygen, no fat could possibly be formed from any one of these substances. The chemical analysis of the constituents of the food of the graminivora shows in the clearest manner that they contain carbon and oxygen in certain proportions; which, when reduced to equivalents, yield the following series:— In vegetable fibrine, albumen, and caseine, there are contained, for 120 eq. carbon, 36 eq. oxygen. In starch 120 100 In cane sugar 120 110 In gum 120 110 In sugar of milk 120 120 In grape sugar 120 140 Now in all fatty bodies there are contained, on an average — For - 120 eq. carb. only 10 eq. oxygen. Since the carbon of the fatty constituents of the animal body is derived from the food, FORMATION OF FAT. 33 seeing that there is no other source whence it can be derived, it is obvious, if we suppose fat to be formed from albumen, fibrine, or casejne, that, for every 120 equivalents of carbon deposited as fat, 26 equivalents of oxygen must be separated from the elements of these substances; and further, if we conceive fat to be formed from starch, sugar, or sugar of milk, that for the same amount of carbon there must be separated 90, 100, and 110 equivalents of oxygen from these compounds respectively. There is, therefore, but one way in which the formation of fat in the animal body is possible, and this is absolutely the same in which its formation in plants takes place; it is a separation of oxygen from the elements of the food. The carbon which we find deposited in the seeds and fruits of vegetables, in the form of oil and fat, was previously a constituent of the atmosphere, and was absorbed by the plant as carbonic acid. Its conversion into fat was accomplished under the influence of light, by the vital force of the vegetable; and the greater part of the oxygen of this carbonic acid was returned to the atmosphere as oxygen gas.* In contradistinction to this phenomenon of vitality in plants, we know that the animal system absorbs oxygen from the atmosphere, and that this oxygen is again given out in combination with carbon or hydrogen; we know, that in the formation of carbonic acid and water, the heat necessary to sustain the constant temperature of the body is produced, and that a process of oxidation is the only source of animal heat. Whether fat be formed by the decomposition of fibrine and albumen, the chief constituents of blood, or by that of starch, sugar, or gum, this decomposition must be accompanied by the separation of oxygen from the elements of these compounds. But this oxygen is not given out in the free state, because it meets in the organism with substances possessing the property of entering into combination with it. In fact, it is given out in the same forms as that which is absorbed from the atmosphere by the skin and lungs. It is easy to see, from the above considerations, that a very remarkable connexion exists between the formation of fat and the respiratory process. XVIII. The abnormal condition, which causes the deposit of fat in the animal body, depends, as was formerly stated, on a disproportion between the quantity of carbon in the food and that of oxygen, absorbed by the skin and lungs. In the normal condition, the quantity of carbon given out is exactly equal to that which is taken in the food, and the body acquires no increase of weight from the accumulation of substances containing much carbon and no nitrogen. * See Appendix, No. 19, on the formation of wix and honey by the bee. 5 If we increase the supply of highly car. bonized food, then the normal state can only be preserved on the condition that, by exercise and labor, the waste of the body is increased, and the supply of oxygen augmented in the same proportion. The production of fat is always a consequence of a deficient supply of oxygen, for oxygen is absolutely indispensable for the dissipation of the excess of carbon in the food. This excess of carbon, deposited in the form of fat, is never seen in the Bedouin or in the Arab of the desert, who exhibits with pride to the traveller his lean, muscular, sinewy limbs, altogether free from fat; but in prisons and jails it appears as a puffiness in the inmates, fed, as they are, on a poor and scanty diet; it appears in the sedentary females of oriental countries; and finally, it is produced under the well known conditions of the fattening of domestic animals. The formation of fat depends on a deficiency of oxygen ; but in this process, in the formation of fat itself, there is opened up a new source of oxygen, a new cause of animal heat. The oxygen set free in the formation of fat is given out in combination with carbon or hydrogen ; and whether this carbon and hydrogen proceed from the substance that yields the oxygen, or from other compounds, still there must have been generated by this formation of carbonic acid or water as much heat as if an equal weight of carbon or hydrogen had been burned in air or in oxygen gas. If we suppose that from 2 equivalents of starch 18 equivalents of oxygen are disengaged, and that these 18 equivalents of oxygen combine with 9 equivalents of carbon, from the bile, for example, no one can doubt that, in this case, exactly as much heat must be developed, as if these 9 equivalents of carbon had been directly burned. In this form, therefore, the disengagement of heat as a consequence of the formation of fat would be undeniable; and it could only be considered hypothetical, on the supposition that carbon and oxygen were disengaged from one and the same substance, in the proportions to yield carbonic acid. If, for example, we suppose that from 2 atoms of starch, C^H^O 10 , the elements of 9 equivalents of carbonic acid are separated, there will remain a compound containing, for 15 equivalents of carbon, 20 of hydrogen and 2 of oxygen; for C 24H!»O20 m c 9 0 19 -f C^H^O*. Or, if we assume that oxygen is separated from starch in the form both of carbonic acid and water, then, after subtracting the elements of 6 equivalents of water and 6 of carbonic acid, there would remain the compound C 18 H"0 2 ; for C24H20O® = C 6 0 12 + H 6 0 6 4- C 18 H w O*. Assuming, then, the separation of oxygen in either of these forms, it remains to be decided whether the carbonic acid and water 34 ANIMAL CHEMISTRY. given off were contained, as such, in the starch, or not. If they were ready formed in the starch, the separation might occur without the disengagement of heat; but if the carbon and hydrogen were present in any other form in the starch, (or in the compound from which the fat was produced,) it is obvious that a change in the arrangement of the atoms must have occurred, in consequence of which the atoms of the carbon and of the hydrogen have united with those of the oxygen, to form carbonic aeid and water. Now, so far as chemical researches have gone, our knowledge of the constitution of starch, and of the varieties of sugar, will j ustify no other conclusion than this, that these substances contain no ready formed carbonic acid. We are acquainted with a large number of processes of metamorphosis of a similar kind, in which the elements of carbonic acid and water are separated from certain preexisting compounds; and we know with certainty that all these processes are accompanied by a disengagement of heat, exactly as if the carbon and hydrogen combined directly with oxygen. Such a disengagement of carbonic acid, for example, occurs in all processes of fermentation or putrefaction, which are, without exception, accompanied with a generation of heat. In the fermentation of a saccharine solution, in consequence of a new arrangement of the elements of the sugar, a certain part of its carbon and oxygen unite to form carbonic acid, which separates as gas; and as another result of this decomposition, we obtain a volatile combustible liquid, containing little oxygen, namely, alcohol. If we add to 2 equivalents of sugar the elements of 12 equivalents of water, and subtract from the sum of the atoms 24 equivalents of oxygen, there remain 6 equivalents of alcohol. (C 24 R u O u + H 12 0 12 ) —0 24 =C 24 H 3e 0 12 = 6 eq. alcohol. These 24 equivalents of oxygen suffice to oxidize completely a third equivalent of sugar—that is, to convert its carbon into carbonic acid and its hydrogen into water, and by this oxidation we recover the 12 equivalents of water supposed to be added in the former part of the process, exactly as if this water had taken no share in it. C «H 12 0 12 -f-0 24 = 12C0 2 -f- 12H0. According to the ordinary view, 12 equivalents of carbonic acid separate from 3 of sugar, yielding 6 of alcohol—that is, exactly the same amount of these products as if twothirds of the sugar had yielded oxygen to the remaining third, so as completely to oxidize its elements. Q36 H 36 0 38_ C a4H360"+ 12C0 2 * * For an explanation of the formula? and equations employed, see the Introduction to the Appendix. By a comparison of these two methods of representing the same change, it will easily be seen that the division or splitting of a compound like sugar into carbonic acid, on the one hand, and a compound containing a little oxygen on the other, is in its results perfectly equivalent to a separation of oxygen from a certain portion of the compound, and the oxidation or combustion of another portion of it at the expense of this oxygen. It is well known that the temperature of a fermenting liquid rises ; and if we assume that a hogshead of wort, holding 1,200 litres = 2,400 lbs., French weight, contains 16 per cent, of sugar, in all 384 lbs., then, during the fermentation of this sugar, an amount of heat must be generated equal to that which would be produced by the combustion of 51 lbs. of carbon. This is equal to a quantity of heat by which every pound of the liquid might be heated by 297-9°; that is, supposing the decomposition of the sugar to occur in a period of time too short to be measured. This is well known not to be the case; the fermentation lasts five or six davs, and each pound of liquid receives the 297*9 degrees of heat during a period of 120 hours. In each hour there is, therefore, set free an amount of. heat capable of raising the temperature of each pound of liquid 1*4 degree; a rise of temperature which is very powerfully counteracted by external cooling and by the vaporization of alcohol and water. The formation of fat, like other analogous phenomena in which oxygen is separated in the form of carbonic acid, is consequently accompanied by a disengagement of heat. This change supplies to the animal body a certain proportion of the oxygen indispensable to the vital processes; and this especially in those cases in which the oxygen absorbed by the skin and lungs is not sufficient to convert into carbonic acid the whole of the carbon adapted for this combination. This excess of carbon, as it cannot be employed to form a part of any organ, is deposited in the cellular tissue in the form of tallow or oil. At every period of animal life, when there occurs a disproportion between the carbon of the food and the inspired oxygen, the latter being deficient, fat must be formed. Oxygen separates from existing compounds, and this oxygen is given out as carbonic acid or water. The heat generated in the formation of these two products contributes to keep up the temperature of the body. Every pound of carbon which obtains the oxygen necessary to convert it into carbonic acid from substances which thereby pass into fat, must disengage as much heat as would raise the temperature of 200 lbs. of water by 70°,—that is, from 32° to 102°. * Thus, in the formation of fat, the vital force possesses a means of counteracting a deficiency in the supply of oxygen, and con* FORMATION OF FAT. 35 sequently in that of the heat indispensable for the vital process. Experience teaches us that in poultry, the maximum of fat is obtained by tying the feet, and by a medium temperature. These animals in such circumstances may be compared to a plant possessing in the highest degree the power of converting all food into parts of its own structure. The excess of the constituents of blood forms flesh and other organized tissues, while that of starch, sugar, &c, is converted into fat. When animals are fattened on food destitute of nitrogen, only certain parts of their structure increase in size. Thus, in a goose, fattened in the method above alluded to, the liver becomes three or four times larger than in the same animal, when well fed with free motion, while we cannot say that the organized structure of the liver is thereby increased. The liver of a goose fed in the ordinary way is firm and elastic; that of the imprisoned animal is soft and spongy. The difference consists in a greater or less expansion of its cells which are filled with fat. In some diseases, the starch, sugar, &c, of the food obviously do not undergo the changes which enable them to assist in respiration, and consequently to be converted into fat. Thus, in diabetes mellitus, the starch is only converted into grape sugar, which is expelled from the body without further change. In other diseases, as for example in inflammation of the fiver, we find the blood loaded with fat and oil; and in the composition of the bile there is nothing at all inconsistent with the supposition that some of its constituents may be transformed into fat. XIX. According to what has been laid down in the preceding pages, the substances of which the food of man is composed may be divided into two classes j into nitrogenized and non-nitrogenized. The former are capable of conversion into blood; the latter incapable of this transformation. Out of those substances which are adapted to the formation of blood are formed all the organized tissues. The other class of substances, in the normal state of health, serve to support the process of respiration. The former may be called the plastic elements of nutrition; the latter, elements of respiration. Among the former we reckon— Vegetable fibrine. Vegetable albumen. Vegetable caseine. Animal flesh. Animal blood. Among the elements of respiration in our food, are— Fat. Pectine. Starch. Bassorine. Gum. Wine. Cane Sugar. Beer. Grape Sugar. Spirits. Sugar of milk. XX. The most recent and exact researches have established as a universal fact, to which nothing yet known is opposed, that the nitrogenized constituents of vegetable food have a composition identical with that of the constituents of the blood. No nitrogenized compound, the composition of which differs from that of fibrine, albumen, and caseine, is capable of supporting the vital process in animals. The animal organism unquestionably possesses the power of forming, from the constituents of its blood, the substance of its membranes and cellular tissue, of the nerves and brain, of the organic part of cartilages and bones. But the blood must be supplied to it ready formed in every thing but its form—that is, in its chemical composition. If this be not done, a period is rapidly put to the formation of blood, and consequently to life. This consideration enables us easily to explain how it happens that the tissues yielding gelatine or chondrine, as, for example, the gelatine of skin or of bones, are not adapted for the support of the vital process ; for their composition is different from that of fibrine or albumen. It is obvious that this means nothing more than that those parts of the animal organism which form the blood do not possess the power of effecting a transformation in the arrangement of the elements of gelatine, or of those tissues which contain it. The gelatinous tissues, the gelatine of the bones, the membranes, the cells, and the skin, suffer, in the animal body, under the influence of oxygen and moisture, a progressive alteration; a part of these tissues is separated, and must be restored from the blood; but this alteration and restoration is obviously confined within very narrow limits. While, in the body of a starving or sick individual, the fat disappears, and the muscular tissue takes once more the form of blood, we find that the tendons and membranes retain their natural condition; the limbs of the dead body retain their connexions, which depend on the gelatinous tissues. On the other hand, we see that the gelatine of bones devoured by a dog entirely disappears, while only the bone earth is found in his excrements. The same is true of man, when fed on food rich in gelatine, as, for example, strong soup. The gelatine is not to be found either in the urine or in the faeces, and consequently must have undergone a change, and must have served some purpose in the animal economy. It is clear, that the gelatine must be expelled from the body in a form different from that in which it was introduced as food. When we consider the transformation of the albumen of the blood into a part of an organ composed of fibrine, the identity in composition of the two subslances renders the change easily conceivable. Indeed we find the change of a dissolved substance into an insoluble organ of vitality, chemically speaking, natural and easily explained, on 36 ANIMAL CHEMISTRY, account of this very identity of composition. Hence the opinion is not unworthy of a closer investigation, that gelatine, when taken in the dissolved state, is again converted, in the body, into cellular tissue, membrane and cartilage; that it may serve for the reproduction of such parts of these tissues as have been wasted, and for their growth. And when the powers of nutrition in the whole body are affected by a change of the health, then, even should the power of forming blood remain the same, the organic force by which the constituents of the blood are transformed into cellular tissue and membranes must necessarily be enfeebled by sickness. In the sick man, the intensity of the vital force, its power to produce metamorphoses, must be diminished as well in the stomach as in all other parts of the body. In this condition, the uniform experience of practical physicians shows that gelatinous matters in a dissolved state exercise a most decided influence on the state of the health. Given in a form adapted for assimilation, they serve to husband the vital force, just as may be done, in the case of the stomach, by due preparation of the food in general. Brittleness in the bones of graminivorous animals is clearly owing to a weakness in those parts of the organism whose function it is to convert the constituents of the blood into cellular tissue and membrane; and if we can trust to the reports of physicians who have resided in the East, the Turkish women, in their diet of rice, and in the frequent use of enemata of strong soup, have united the conditions necessary for the formation both of cellular tissue and of fat. PART II. THE METAMORPHOSIS OF TISSUES. 1. The absolute identity of composition in the chief constituents of blood and the nitrogenized compounds in vegetable food would, some years ago, have furnished a plausible reason for denying the accuracy of the chemical analysis leading to such a result. At that period, experiment had not as yet demonstrated the existence of numerous compounds, both containing nitrogen and devoid of that element, which with the greatest diversity in external characters, yet possess the very same composition in 100 parts; nay, many of which even contain the same absolute amount of equivalents of each element. Such examples are now very frequent, and are known by the names of isomeric and polymeric compounds. 2. Cyanunc acid, for example, is a nitrogenized compound which crystallizes in beautiful transparent octahedrons, easily soluble in water and in acids, and very permanent. Cyamelide is a second body, absolutely insoluble in water and acids, white and opaque like porcelain or magnesia. Hydrated cyanic acid is a third compound, which is a liquid more volatile than pure acetic acid, which blisters the skin, and cannot be brought in contact with water without being instantaneously resolved into new products. These three substances not only yield, on analysis, absolutely the same relative weights of the same elements, but they may be converted and reconverted into one another, even in hermetically closed vessels —that is, without the aid of any foreign matter. (See Appendix, 21.) Again, among those substances which contain no nitrogen, we have aldehyde, a combustible liquid miscible with water, which boils at the temperature of the hand, attracts oxygen from the atmosphere with avidity, and is thereby changed into acetic acid. This compound cannot be preserved, even in close vessels; for after some hours or days, its consistence, its volatility, and its power of absorbing oxygen, all are changed. It deposits long, hard, needle-shaped crystals, which at 212° are not volatilized, and the supernatant liquid is no longer aldehyde. It now boils at 140°, cannot be mixed with water, and when cooled to a moderate degree crystallizes in a form like ice. Nevertheless, analysis has proved, that these three bodies, so different ID their characters, are identical in composition. (21.) 3. A similar group of three occurs in the case of albumen, fibrine, and caseine. They differ in external character, but contain exactly the same proportions of organic elements. When animal albumen, fibrine, and caseine are dissolved in a moderately strong solution of caustic potash, and the solution is exposed for some time to a high temperature, these substances are decomposed. The addition of acetic acid to the solution causes, in all three, the separation of a gelatinous translucent precipitate, which has exactly the same characters and composition, from whichever of the three substances above mentioned it has been obtained. Mulder, to whom we owe the discovery of this compound, found, by exact and careful analysis, that it contains the same organic elements, and exactly in the same proportion, as the animal matters from which it is prepared; insomuch, that if we deduct from the analysis of albumen, fibrine, and caseine, the ashes they yield when incinerated, as well as the sulphur and phosphorus they contain, and then calculate the remainder for 100 parts, we obtain the same result as DIGESTION COMPARED TO FERMENTATION. 37 in the analysis of the precipitate above described, prepared by potash, which is free from inorganic matter. (22.j) Viewed in this light, the chief constituents of the blood and the caseine of milk may be regarded as compounds of phosphates and other salts, and of sulphur and phosphorus, with a compound of carbon, nitrogen, hydrogen, and oxygen, in which the relative proportion of these elements is invariable; and this compound may be considered as the commencement and starting point of all other animal tissues, because these are all produced from the blood. These considerations induced Mulder to give to this product of the decomposition of albumen, &c, by potash, the name of proteine (from " I take the first rank.") The blood, or the constituents of the blood, are consequently compounds of this proteine with variable proportions of inorganic substances. Mulder further ascertained, that the insoluble nitrogenized constituent of wheat flour (vegetable fibrine,) when treated with potash, yields the very same product, proteine; and it has recently been proved that vegetable albumen and caseine are acted on by potash precisely as animal albumen and caseine are. 4. As far, therefore, as our researches have gone, it may be laid down as a law, founded on experience, that vegetables produce, in their organism, compounds of proteine ; and that out of these compounds of proteine the various tissues and parts of the animal body are developed by the vital force, with the aid of the oxygen of the atmosphere and of the elements of water.* Now, although it cannot be demonstrated that proteine exists ready formed in these vegetable and animal products, and although the difference in their properties seems to indicate that their elements are not arranged in the same manner, yet the hypothesis of the pre-existence of proteine, as a point of departure in developing and comparing their properties, is exceedingly convenient. At all events it is certain that the elements of these compounds assume the same arrangements when acted on by potash at a high temperature. All the organic nitrogenized constituents of the body, how different soever they may be in composition, are derived from proteine. They are formed from it, by the addition or subtraction of the elements of water or of oxygen, and by resolution into two or more compounds. * The experiment of Tiedemann and Gmelin, who found it impossible to sustain the life of geese by means of boiled white of egg, may be easily explained, when we reflect that a graminivorous animal, especially when deprived of free motion, cannot obtain, from the transformation or waste of the tissues alone, enough of carbon for the respiratory process. 2 lbs. of albumen contain only oz. of carbon, of which, among the last products of transformation, a fourth part is given off in the form of uric acid. 5. This proposition must be received as an undeniable truth, when we reflect on the developement of the young animal in the egg of a fowl. The egg can be shown to contain no other nitrogenized compound except albumen. The albumen of the yolk is identical with that of the white; (23) the yolk contains, besides, only a yellow fat, in which cholesterine and iron may be detected. Yet we see in the process of incubation, during which no food and no foreign matter, except the oxygen of the air, is introduced, or can take part in the developement of the animal, that out of the albumen, feathers, claws, globules of the blood, fibrine, membrane and cellular tissue, arteries and veins, are produced. The fat of the yolk may have contributed, to a certain extent, to the formation of the nerves and brain; but the carbon of this fat cannot have been employed to produce the organized tissues in which vitality resides, because the albumen of the white and of the yolk already contains, for the quantity of nitrogen present, exactly the proportion of carbon required for the formation of these tissues. 6. The true starting-point for all the tissues is, consequently, albumen; all nitrogenized articles of food, whether derived from the animal or from the vegetable kingdom, are. converted into albumen before they can take part in the process of nutrition. All the food consumed by an animal becomes in the stomach soluble, and capable of entering into the circulation. In the process by which this solution is effected, only one fluid, besides the oxygen of the air, takes a part; it is that which is secreted by the lining membrane of the stomach. The most decisive experiments of physiologists have shown that the process of chymification is independent of the vital force; that it takes place in virtue of a purely chemical action, exactly similar to those processes of decomposition or transformation which are known as putrefaction, fermentation or decay (eremacausis). 7. When expressed in the simplest form, fermentation, or putrefaction, may be described as a process of transformation—that is, a new arrangement of the elementary particles, or atoms, of a compound, yielding two or more new groups or compounds, and caused by contact with other substances, the elementary particles of which are themselves in a state of transformation or decomposition. It is a communication, or an imparting of a state of motion, which the atoms of a body in a state of motion are capable of producing in other bodies, whose elementary particles are held together only by a feeble attraction. . 8. Thus the clear gastric juice contains a substance in a state of transformation, by the contact of which with those constituents of the food which, by themselves, are insoluble in water, the latter acquire, in virtue of a new grouping of their atoms, the pro- 38 ANIMAL CHEMISTRY. perty of dissolving in that fluid. During digestion, the gastric juice, when separated, i3 found to contain a free mineral acid, the presence of which checks all further change. That the food is rendered soluble quite independently of the vitality of the digestive organs has been proved by a number of the most beautiful experiments. Food, enclosed in perforated metallic tubes, so that it could not come into contact with the stomach, was found to disappear as rapidly, and to be as perfectly digested, as if the covering had been absent; and fresh gastric juice, out of the body, when boiled white of egg, or muscular fibre, were kept in contact with it for a time, at the temperature of the body, caused these substances to lose the solid form and to dissolve in the liquid. 9. It can hardly be doubted that the substance which is present in the gastric juice in a state of change is a product of the transformation of the stomach itself. No substances possess, in so high a degree as those arising from the progressive decomposition of the tissues containing gelatine or chondrine, the property of exciting a change in the arrangement of the elements of other compounds. When the lining membrane of the stomach of any animal, as, for example, that of the calf, is cleaned by continued washing with water, it produces no effect whatever, if brought into contact with a solution of sugar, with milk or other substances. But if the same membrane be exposed for some time to the air, or dried, and then placed in contact with such substances, the sugar is changed, according to the state of decomposition of the animal matter, either into lactic acid, into mannite and mucilage, or into alcohol and carbonic, acid; while milk is instantly coagulated. An ordinary animal bladder retains, when dry, all its properties unchanged; but when exposed to air and moisture, it undergoes a change not indicated by any obvious external signs. If, in this state, it be placed in a solution of sugar of milk, that substance is quickly changed into lactic acid. 10. The fresh lining membrane of the stomach of a calf, digested with weak muriatic acid, gives to this fluid no power of dissolving boiled flesh or coagulated white of egg. But if previously allowed to dry, or if left for a time in water, it then yields, to water acidulated with muriatic acid, a substance in minute quantity, the decomposition of which is already commenced, and is completed in the solution. If coagulated albumen be placed in this solution, the state of decomposition is communicated to it, first at the edges, which become translucent, pass into a mucilage, and finally dissolve. The same change gradually affects the whole mass, and at last it is entirely dissolved, with the exceptiou of fatty particles, which render the solution turbid. Oxygen is conveyed to every part of the body by the arterial blood; moisture is every where present; and thus we have united the chief conditions of ail transformations in the animal body. Thus, as in the germination of seeds, the presence of a body in a state of decomposition or transformation, which has been called diastase, effects the solution of the starch—that is, its conversion into sugar; so, a product of the metamorphosis of the substance of the stomach, being itself in a state of metamorphosis which is completed in the stomach, effects the dissolution of all such parts of the food as are capable of assuming a soluble form. In certain diseases, there are produced from the starch, sugar, &c, of the food, lactic acid and mucilage. (24.) These are the very same products which we can produce out of sugar by means of membrane in a state of decomposition out of the body; but in a normal state of health, no lactic acid is formed in the stomach. 11. The property possessed by many substances, such as starch and the varieties of sugar, by contact Avith animal substances in a state of decomposition, to pass into lactic acid, has induced physiologists, without farther inquiry, to assume the fact of the production of lactic acid during digestion; and the power which this acid has of dissolving phosphate of lime has led them to ascribe to it the character of a general solvent. But neither Prout nor Braconnot could detect lactic acid in the gastric juice; and even Lehmann (see his " Lehrbuch der Physiologischen Chemie," torn. i. p. 285) obtained from the gastric juice of a cat only microscopic crystals, which he took for lactate of zinc, although their chemical character could not be ascertained. The presence of free muriatic acid in the gastric juice, first observed by Prout, has been confirmed by all those chemists who have examined that fluid since. This muriatic acid is obviously derived from common salt, the soda of which plays a very decided part in the conversion of fibrine and caseine into blood. Muriatic acid yields to no other acid in the power of dissolving bone earth, and even acetic acid, in this respect, is equal to lactic acid. There is consequently no proof of the necessity of lactic acid in the digestive process; and we know with certainty, that in artificial digestion it is not formed. Berzelius indeed has found lactic acid in the blood and flesh of animals; but when his experiments were made, chemists were ignorant of the extraordinary facility and rapidity with which this acid is formed from a number of substances containing its elements, when in contact with animal matter. In the gastric juice of a dog, Braconnot found, along with free muriatic acid, distinct traces of a salt of iron, which he at first held to be an accidental admixture. But in the gastric juice of a second dog, collected with the utmost care, the iron was again found. (Ann. de Ch. et de Ph. lix. p. 249.) NITROGEN EXHALED PROM THE LUNGS. 39 This occurrence of iron is full of significance in regard to the formation of the blood. 12. In the action of the gastric juice on the food, no other element takes a share, except the oxygen of the atmosphere and the elements of water. This oxygen is introduced directly into the stomach. During the mastication of the food, there is secreted into the mouth from organs specially destined to this function, a fluid, the saliva, which possesses the remarkable property of enclosing air in the shape of froth, in a far higher degree than even soapsuds. This air, by means of the saliva, reaches the stomach with the food, and there its oxygen enters into combination, while its nitrogen is given out through the skin and lungs. The longer digestion continues, that is, the greater resistance offered to the solvent action by the food, the more saliva, and consequently the more air enters the stomach. Rumination, in certain graminivorous animals, has plainly for one object a renewed and repeated introduction of oxygen; for a more minute mechanical division of the food only shortens the time required for solution. The unequal quantities of air which reach the stomach with the saliva in different classes of animals explain the accurate observations made by physiologists, who have established beyond all doubt the fact, that animals give out pure nitrogen through the skin and lungs, in variable quantity. This fact, is so much the more important, as it furnishes the most decisive proof, that the nitrogen of the air is applied to no use in the animal economy. The fact that nitrogen is given out by the skin and lungs, is explained by the property which animal membranes possess of allowing all gases to permeate them, a property which can be shown to exist by the most simple experiments. A bladder, filled with carbonic acid, nitrogen, or hydrogen gas, if tightly closed and suspended in the air, loses in 24 hours the whole of the enclosed gas; by a kind of exchange, it passes outwards into the atmosphere, while its place is occupied by atmospherical air. A portion of intestine, a stomach, or a piece of skin or membrane, acts precisely as the bladder, if filled with any gas. This permeability to gases is a mechanical property, common to all animal tissues; and it is found in the same degree in the living as in the dead tissue. It is known that in cases of wounds of the lungs a peculiar condition is produced, in which, by the act of inspiration, not only oxygen but atmospherical air, with its whole amount (£ths) 0 f nitrogen, penetrates into the cells of the lungs. This air is carried by the circulation to every part of the body, so that every part is inflated or puffed up with the air, as with water in dropsy. This state ceases, without pain, as soon as the entrance'of the air through the wound is stopped. There can be no doubt that the oxygen of the air, thus accumulated in the cellular tissue, enters into combination, while its nitrogen is expired through the skin and lungs. Moreover, it is well known that in many graminivorous animals, when the digestive organs have been overloaded with fresh juicy vegetables, these substances undergo in the stomach the same decomposition as they would at the same temperature out of the body. They pass into fermentation and putrefaction, whereby so great a quantity of carbonic acid gas and of inflammable gas is generated, that these organs are enormously distended, sometimes even to bursting. From the structure of their stomach or stomachs, these gases cannot escape through the oesophagus ; but in the course of a few hours, the distended body of the animal becomes less swollen, and at the end of twentyfour hours no trace of the gases is left. (25.) Finally, if we consider the fatal accidents which so frequently occur in wine countries from the drinking of what is called featherwhite wine (derfederweisse Wein,) we can no longer doubt that gases of every kind, whether soluble or insoluble in water, possess the property of permeating animal tissues, as water penetrates unsized paper. This poisonous wine is wine still in a state of fermentation, which is increased by the heat of the stomach. The carbonic acid gas which is disengaged penetrates through the parietes of the stomach, through the diaphragm, and through all the intervening membranes, into the air-cells of the lungs, out of which it displaces the atmospherical air. The patient dies with all the symptoms of asphyxia caused by an irrespirable gas; and the surest proof of the presence of the carbonic acid in the lungs is the fact, that the inhalation of ammonia (which combines with it) is recognized as the best antidote against this kind of poisoning. The carbonic acid of effervescing wines and of soda-water, when taken into the stomach, or of water saturated with this gas, administered in the form of enema, is given out again through the skin and lungs ; and this is equally true of the nitrogen which is introduced into the stomach with the food in the saliva. No doubt a part of these gases may enter the venous circulation through the absorbent and lymphatic vessels, and thus reach the lungs, where they are exhaled; but the presence of membranes offers not the slightest obstacle to their passing directly into the cavity of the chest. It is, in fact, difficult to suppose that the absorbents and lymphatics have any peculiar tendency to absorb air, nitrogen or hydrogen, and convey these gases into the circulation, since the intestines, the stomach, and all spaces in the body not filled with solid or liquid matters, contain gases, which only quit their position when their volume exceeds a certain point, and which, consequently, are not absorbed. 40 ANIMAL CHEMISTRY. More especially in reference to nitrogen, we must suppose that it is removed from the stomach by some more direct means, and not by the blood, which fluid must already, in passing through the lungs, have become saturated with that gas, that is, must have absorbed a quantity of it, proportioned to its solvent power, like any other liquid. By the respiratory motions, all the gases which fill the otherwise empty spaces of the body are urged towards the chest; for by the motion of the diaphragm and the expansion of the chest a partial vacuum is produced, in consequence of which air is forced into the chest from all sides by the atmospheric pressure. The equilibrum is, no doubt, restored, for the most part, through the windpipe, but all the gases in the body must, nevertheless, receive an impulse towards the chest. In birds and tortoises these arrangements are reversed. If we assume that a man introduces into the stomach in each minute only £th of a cubic inch of air with the saliva, this makes in eighteen hours 135 cubic inches; and if £th be deducted as oxygen, there will still remain 108 cubic inches of nitrogen, which occupy the space of 3 lbs. of water. Now whatever may be the actual amount of the nitrogen thus swallowed, it is certain that the whole of it is given out again by the mouth, nose, and skin ; and when we consider the very large quantity of nitrogen found in the intestines of executed criminals by Magendie, as well as the entire absence of oxygen in these organs, (26,) we must assume that air, and consequently nitrogen, enters the stomach by resorption through the skin, and is afterwards exhaled by the lungs. When animals are made to respire in gases containing no nitrogen, more of that gas is exhaled, because in this case the nitrogen within the body acts towards the external space as if the latter were a vacuum. (See Graham " On the Diffusion of Gases.") The differences in the amount of expired nitrogen in different classes of animals are thus easily explained; the herbivora swallow with the saliva more air than the carnivora; they expire more nitrogen than the latter, —less when fasting than immediately after taking food. 13. In the same way as muscular fibre, when separated from the body, communicates the state of decomposition existing in its elements to the peroxide of hydrogen, so a certain product, arising by means of the vital process, and in consequence of the transposition of the elements of parts of the stomach and of the other digestive organs, while its own metamorphosis is accomplished in the stomach, acts on the food. The insoluble matters become soluble—they are digested. It is certainly remarkable, that hard-boiled white of egg, or fibrine, when rendered soluble by certain liquids, by organic acids, or weak alkaline solutions, retain all their properties except the solid form (cohesion) without the slightest change. Their elementary molecules, without doubt assume a new arrangement; they do not, however, separate into two or more groups, but remain united together. The very same thing occurs in the digestive process; in the normal state, the food only undergoes a change in its state of cohesion, becoming fluid without any other change of properties. The greatest obstacle to forming a clear conception of the nature of the digestive process, which is here reckoned among those chemical metamorphoses which have been called fermentation and putrefaction, consists in our involuntary recollection of the phenomena which accompany the fermentation of sugar and of animal substances, (putrefaction,) which phenomena we naturally associate with any similar change; but there are numberless cases in which a complete chemical metamorphosis of the elements of a compound occurs without the smallest disengagement of gas, and it is chiefly these which must be borne in mind, if we would acquire a clear and accurate idea of the chemical notion or conception of the digestive process. All substances which can arrest the phenomena of fermentation and putrefaction in liquids, also arrest digestion when taken into the stomach. The action of the empyreumatic matters in coffee and tobacco smoke, of creosote, of mercurials, &c., &c, is on this account worthy of peculiar attention with reference to dietetics. The identity in composition of the chief constituents of blood and of the nitrogenized constituents of vegetable food has certainly furnished, in an unexpected manner, an explanation of the fact that putrefying blood, white of egg, flesh, and cheese produce the same effects in a solution of sugar as yeast or ferment; that sugar, in contact with these substances, according to the particular stage of decomposition in which the putrefying matters may be, yields, at one time, alcohol and carbonic acid; at another, lactic acid, mannite, and mucilage. The explanation is simply this, that ferment, or yeast, is nothing but vegetable fibrine, albumen, or caseine in a state of decomposition, these substances having the same composition with the constituents of flesh, blood, or cheese. The putrefaction of these animal matters is a process identical with the metamorphosis of the vegetable matters identical with them ; it is a separation or splitting up into new and less complex compounds. And if we consider the transformation of the elements of the animal body (the waste of matter in animals) as a chemical process which goes on under the influence of the vital force, then the putrefaction of animal matters out of the body is a division into simpler compounds, in which the vital force takes no share. The action in both cases is the same, only the products differ. The practice of medicine has furnished the COMPOSITION OP FIBRINE &c. 41 most beautiful and interesting observations on the action of empyreumatic substances, such as wood, vinegar, creosote, &c, on malignant wounds and ulcers. In such morbid phenomena two actions are going on together; one metamorphosis, which strives to complete itself under the influence of the vital force, and another, independent of that force. The latter is a chemical process, which is entirely suppressed or arrested by empyreumatic substances; and this effect is precisely opposed to the poisonous influence exercised on the organism by putrefying blood when introduced into a fresh wound. 14. The formula C H 36 N 6 0 M * is that which most accurately expresses the composition of proteine, or the relative proportions of the organic elements in the blood, as ascertained by analysis. Albumen, fibrine, and caseine contain proteine; caseine contains, besides, sulphur, but no phosphorus ; albumen and fibrine contain both these substances chemically combined—the former more sulphur than the latter. We cannot directly ascertain in what form the phosphorus exists. But we have decided proof that the sulphur cannot be in the oxidized state. All these substances, when heated with a moderately strong solution of potash, yield the sulphur which we find in the solution as sulphuret of potassium ; and on the addition of an acid it is given off as sulphuretted hydrogen. When pure fibrine or ordinary albumen is dissolved in a weak solution of potash, and acetate of lead is added to the solution, in such proportion that the whole of the oxide of lead remains dissolved in the potash, the mixture, if heated to the boiling point, becomes black like ink, and sulphuret of lead is deposited as a fine black powder. It is extremely probable, that by the action of the alkali the sulphur is removed as sulphuretted hydrogen, the phosphorus as phosphoric or phosphorus acid. Since, in this case, sulphur and phosphorus are eliminated on the one hand, and oxygen and hydrogen on the other, it might be concluded that fibrine and albumen, when analyzed with their sulphur and phosphorus, would yield a larger proportion of oxygen and hydrogen than is found in proteine. But this cannot be shown in the analysis; for fibrine, for example, has been found to contain 0*36 per cent, of sulphur. Assuming, then, that this sulphur is eliminated by the alkali in combination with hydrogen, proteine would yield 0*0225 per cent, less hydrogen than fibrine; instead of the mean amount of 7"062 per cent, of hydrogen, the proteine should yield 7*04 per cent. In like manner, by the elimination of the phosphorus in combination with oxygen, the amount of oxygen in fibrine would be reduced from 22-715—22 00 per cent, to 22-5— * For the method of converting this and other formula into proportions per cent., see Appendix. 6 21*8 per cent, in proteine. But the limits of error in' our analyses are, on an average, beyond per cent, in the hydrogen, and beyond per cent, in the oxygen ; while in the supposed case the difference in the hydrogen would not be greater than per cent. Finally, if we reflect, that the elimination of oxygen and hydrogen with the sulphur and phosphorus does not exclude the addition of the elements of water, and if we assume that fibrine and albumen, in passing into proteine,- do combine with a certain quantity of water, an occurrence which is highly probable, we shall see that there is no probability that the ultimate analysis of these compounds shall ever enable us to decide such questions, or to fix the chemical view of the relation of proteine to albumen, fibrine, or caseine, farther than has been done above. Some have endeavoured to prove the existence of unoxidized phosphorus in albumen and fibrine from the formation of sulphuret of potassium when they are acted on by potash, supposing the oxygen of the potash to have formed phosphoric acid with the phosphorus; but caseine, which contains no phosphorus, yields sulphuret of potassium, just like the other substances; and here its formation cannot be accounted for, unless we admit the previous production of sulphuretted hydrogen. In the mere boiling of flesh, for the purpose of making soup, sulphuretted hydrogen, as Chevreul has shown, is disengaged. Moreover, the proportion of sulphur, for the same amount of phosphorus, is not the same in fibrine and albumen, from which no other conclusion can be drawn, but that the formation of sulphuret of potassium has no relation to the presence of phosphorus. Sulphuret of potassium is formed from caseine, which is not supposed to contain any uncombined phosphorus; and it is formed, also, from albumen, which contains only half as much phosphorus as fibrine. Every attempt to give the true absolute amount of the atoms in fibrine and albumen in a rational formula, in which the sulphur and phosphorus are taken, not in fractions, but in entire equivalents, must be fruitless, because we are absolutely unable to determine with perfect accuracy the exceedingly minute quantities of sulphur and phosphorus in such compounds; and because a variation in the sulphur or phosphorus, smaller in extent than the usual limit of errors of observation, will affect the number of atoms of carbon, hydrogen, or oxygen to the extent of 10 atoms or more. We must be careful not to deceive ourselves in our expectations of what chemical analysis can do. We know, with certainty, that ihe numbers representing the relative proportions of the organic elements are the same in albumen and fibrine, and hence we conclude that they have the same composition. This conclusion is not affected by the 42 ANIMAL CHEMISTR i fact, that we do not know the absolute number of the atoms of their elements, which have united to form the compound atom. 15. A formula for proteine is nothing more than the nearest and most exact expression in equivalents, of the result of the best analyses; it is a fact established so far, free from doubt, and this alone is, for the present, valuable to us. If we reflect, that from the albumen and fibrine of the body all the other tissues are derived, it is perfectly clear that this can only occur in two ways. Either certain elements have been added to, or removed from, their constituent parts. If we now, for example, lock for an analytical expression of the composition of cellular tissue, of the tissues yielding gelatine, or tendons, of hair, of horn, &c, in which the number of atoms of carbon is made invariably the same as in albumen and fibrine, we can then see at the first glance, in what way the proportion of the other elements has been altered; but this includes all that physiology requires in order to obtain an insight into the true nature of the formative and nutritive processes in the animal body. From the researches of Mulder and Scherer we obtain the following empirical formulae. Composition of organic tissues. Albumen . . . Fibrine . . . C 48 iN 6 H 36 0 14 -|-P-f-2S Caseine . . . C 48 N 6 H 36 0 ,4 -fS Gelatinous tissues, > p 4 8iv7.5T-T4ini8 tendons £ * V iN n U Chondrine. . . C 4S N 6 H 40 O 20 Hair, horn. . . C 48 N 7 H 38 0 1T Arterial membrane . CWH^O 16 The composition of these formula? shows, that when proteine passes into chondrine, (the substance of the cartilages of the ribs,) the elements of water, with oxygen, have been added to it; while in the formation of the serous membranes, nitrogen also has entered into combination. If we represent the formula of proteine, C 48 N 6 H 36 0 14 by Pr, then nitrogen, hydrogen, and oxygen have been added to it in the form of known compounds, and in the following proportions, in forming the gelatinous tissues, hair, horn, arterial membrane, &c. Proteine. Ammonia. Water. Oxygen. Fibrine, Albumen Pr Arterial Membrane Pr . -f-2HO. Chondrine . . Pr . +4HO.+20. Hair, horn . . Pr-f- NH 3 . . +30. Gelatinous tissues 2Pr-f-3NH 3 -}- H0.+70. 17. From this general statement it appears that all the tissues of the body contain, for the same amount of carbon, more oxygen than the constituents of blood. During their formation, oxygen, either from the atmosphere or from the elements of water, has been added to the elements of proteine. In * The quantities of sulphur and phosphorus here expressed by S and P are not equivalents, but only give the relative proportions of these two elements to each other, as found by analysis. hair and gelatinous membrane we observe, farther, an excess of nitrogen and hydrogen, and that in the proportions to form ammonia. Chemists are not yet. agreed on the question, in what manner the elements of sulphate of potash are arranged; it would therefore be going too far, were they to pronounce arterial membrane a hydrate of proteine, chondrine a hydrated oxide of proteine, and hair and membranes compounds of ammonia with oxides of proteine. The above formulae express with precision the differences of composition in the chief constituents of the animal body; they show, that for the same amount of carbon the proportion of the other elements varies, and how much more oxygen or nitrogen one compound contains than another. 18. By means of these formulae we can trace the production of the different compounds from .the constituents of blood; but the explanation of their production may take two forms, and we have to decide which of these comes nearest to the truth. For the same amount of carbon, membranes and the tissues which yield gelatine contain more nitrogen, oxygen, and hydrogen than proteine. It is conceivable that they are formed from albumen by the addition of oxygen, of the elements of water, and of those of ammonia, accompanied by the separation of sulphur and phosphorus; at all events, their composition is entirely different from that of the chief constituents of blood. The action of caustic alkalies on the tissues yielding gelatine shows distinctly that they no longer contain proteine; that substance cannot in any way be obtained from them; and all the products formed by the action of alkalies on them differ entirely from those produced by the compounds of proteine in the same circumstances. Whether proteine exist, ready formed, in fibrine, albumen, and caseine, or not, it is certain that their elements, under the influence of the alkali, arrange themselves so as to form proteine; but this property is wanting in the elements of the tissues which yield gelatine. The other, and perhaps the more probable explanation of the production of these tissues from proteine, is that which makes it dependent on a separation of carbon. If we assume the nitrogen of proteine to remain entire in the gelatinous tissue, then the composition of the latter calculated on 6 equivalents of nitrogen, would be represented by the formula, WW 4 . This formula approaches most closely to the analysis of Scherer, although it is not an exact expression of his results. A formula corresponding more perfectly to the analysis, is C^WH^O 12 ; or calculated according to Mulder's analysis, C^H^O 20 .* * The formula C^NsH^O 20 , adopted by Mul' der, gives, when reduced to 100 parts, too little | nitrogen to be considered an exact expression of 1 his analyses. METAMORPHOSIS OF TISSUES. 43 According to the first formula, carbon and hydrogen have been separated; according to the two last, a certain proportion of all the elements has been removed 19. We must admit, as the most important result of the study of the composition of gelatinous tissue, and as a point undeniably established, that, although formed from compounds of proteine, it no longer belongs to the series of the compounds of proteine. Its chemical characters and composition justify this conclusion. No fact is as yet opposed to the law, deduced from observation, that nature has exclusively destined compounds of proteine for the production of blood. No substance analogous to the tissues yielding gelatine is found in vegetables. The gelatinous substance is not a compound of proteine; it contains no sulphur, no phosphorus, and it contains more nitrogen or less carbon than proteine. The compounds of proteine, under the influence of the vital energy of the organs which form the blood, assume a new form, but are qot altered in composition; while these organs, as far as our experience reaches, do not possess the power of producing compounds of proteine, by virtue of any influence, out of substances which contain no proteine. Animals which are fed exclusively with gelatine, the most highly nitrogenized element of the food of carnivora, died with the symptoms of starvation; in short, the gelatinous tissues are incapable of conversion into blood. But there is no doubt that these tissues are formed from the constituents of the blood; and we can hardly avoid entertaining the supposition, that the fibrine of venous blood, in becoming arterial fibrine, passes through the first stage of conversion into gelatinous tissue. We cannot, with much probability, ascribe to membranes and tendons the power of forming themselves out of matters brought by the blood; for how could any matter become a portion of the cellular tissue, for example, by virtue of a force which has as yet no organ ? An already existing cell may possess the power of reproducing or of multiplying itself, but in both cases the presence of a substance identical in composition with cellular tissue is essential. Such matters are formed in the organism, and nothing can be better fitted for their production than the substance of the cells and membranes which exist in animal food, and become soluble in the stomach during digestion, or which are taken by man in a soluble form. 20. In the following pages I offer to the reader an attempt to develope analytically the principal metamorphoses which occur in the animal body; and, to preclude all misapprehension, I do this with a distinct protest against all conclusions and deductions which may now or at any subsequent period be derived from it in opposition to the views developed in the preceding part of this work, with which it has no manner of connexion. The results here to be described have surprised me no less than they will others, and have excited in my mind the same doubts as others will conceive; but they are not the creations of fancy, and I give them because I entertain the deep conviction that the method which has led to them is the only one by which we can hope to acquire insight into the nature of the organic processes. The numberless qualitative investigations of animal matters which are made are equally worthless for physiology and for chemistry, so long as they are not instituted with a well defined object, or to answer a question clearly put. If we take the letters of a sentence which we wish to decipher, and place them in a fine, we advance not a step towards the discovery of their meaning. To resolve an enigma, we must have a perfectly clear conception of the problem. There are many ways to the highest pinnacle of a mountain; but those only can hope to reach it who keep the summit constantly in view. All our labour and all our efforts, if we strive to attain it through a morass, only serve to cover us more completely with mud; our progress is impeded by difficulties of our own creation, and at last even the greatest strength must give way when so absurdly wasted. 21. If it be true that all parts of the body are formed and developed from the blood or the constituents of the blood, that the existing organs at every moment of life are transformed into new compounds under the influence of the oxygen introduced in the blood, then the animal secretions must of necessity contain the products of the metamorphosis of the tissues. 22. If it be further true, that the urine contains those products of metamorphosis which contain the most nitrogen, and the bile those which are richest in carbon, from all the tissues which in the vital process have been transformed into unorganized compounds, it is clear that the elements of the bile and of the urine, added together, must be equal in the relative proportion of these elements to the composition of the blood. 23. The organs are formed from the blood, and contain the elements of the blood; they become transformed into new compounds, with the addition only of oxygen and of water. Hence the relative proportion of carbon and nitrogen must be the same as in the blood. If then we subtract from the composition of blood the elements of the urine, then the remainder, deducting the oxygon and water which have been added, must give the composition of the bile. Or if from the elements of the blood, we subtract the elements of the bile, the remainder must give the composition of urate of ammonia, or of urea and carbonic acid. It will surely appear remarkable that this manner of viewing the subject has led to the true formula of bile, or, to speak more accu- 44 ANIMAL CHEMISTRY rately, to the most correct empirical expression of its composition; and has furnished the key to its metamorphoses, under the influence of acids and alkalies, which had previously been sought for in vain. 24. When fresh drawn blood is made to trickle over a plate of silver, heated to 140°, it dries to a red, varnish-like matter, easily reduced to powder. Muscular flesh, free from fat, if dried first in a gentle heat, and then at 212°, yields a brown, pulverizable mass. The analyses of Play fair and Boeckmann (28) give for flesh (fibrine, albumen, cellular tissue, and nerves) and for blood, as the most exact expression of their numerical results, one and the same formula, namely, C«N 6 H 39 0 15 . This may be calIed the em _ pirical formula of blood. 25. The chief constituent of bile, according to the researches of Demarcay, is a compound, analogous to soaps, of soda with a peculiar substance, which has been named choleic acid. This acid is obtained in combination with oxide of lead, when bile, purified by means of alcohol from all matters insoluble in that menstruum, is mixed with acetate of lead. Choleic acid is resolved, by the action of muriatic acid, into ammonia, taurine, and a new acid, choloidic acid, which contains no nitrogen. When boiled with caustic potash, choleic acid is resolved into carbonic acid, ammonia, and another new acid, cholic acid (distinct from the cholic acid of Gmelin.) Now it is clear that the true formula of choleic acid must include the analytical expression of these modes of decomposition; in other words, that it must enable us to show that the composition of the products derived from it is related in a clear and simple manner, to the composition of the acid itself. This is the only satisfactory test of a formula; and the analytical expression thus obtained loses nothing of its truth or value, if it should appear, as the researches of Berzelius seem to show, that choleic and choloidic acids are mixtures of different compounds ; for the relative proportions of the elements cannot in any way be altered by this circumstance. 26. In order to develope the metamorphoses which choleic acid suffers under the influence of acids and alkalies, the following formula alone can be adopted as the empirical expression of the results of its analysis, Formula of choleic acid: C^N 8 !! 66 ©**. (29) I repeat, that this formula may express the composition of one, or of two or more compounds; no matter of how many compounds the so-called choleic acid may be made up, the above formula represents the relative proportions of all their elements taken together. If now we subtract from the elements of choleic acid, the products formed by the action of muriatic acid, namely, ammonia and taurine, we obtain the empirical formula of choloidic acid. Thus: from the Formula of choleic acid C'WH^O 8 Substract— 1 at. taurine C 4 NH 7 0 10 1 £ C 4]\-2hioo"> 1 eq. ammonia NH 3 J ( There remains the formula of choloidic acid —C 72 H"O»(30.) 27. Again, if from the formula of choleic acid we subtract the elements of urea and 2 atoms of water (=2 eq. carbonic acid and 2 eq. ammonia,) there will remain the formula and composition of cholic acid. Thus: from the Formula of choleic acid — Substract— 2 eq. car. acid -C«OJ ) _ C a N2 H e Q4 2 eq. ammonia = N 2 H 6 J Remains the formula of cholic acid «=C 74 H 60 O 18 (31.) When we consider the very close coincidence between these formulae and the actual results of analysis (see Appendix, 29, 30, 31,) it is scarcely possible to doubt that the formula above adopted for choleic acid expresses, as accurately as is to be expected in the analysis of such compounds, the relative proportion of its elements, no matter in how many different forms they may be united to produce that acid. 28. Let us now add the half of the numbers which represent the formula of choleic acid, to the elements of the urine of serpents—that is, to neutral urate of ammonia, as follows: i the formula of choleic acid —C««N 1 H M 0 11 Add to this— 1 eq. uric acid *=C 10 N 4 H 4 O 6 ? ruwmvne leq. ammonia — NH 3 $ The sum is —C«N 6 H«0» 29. But this last formula expresses the composition of blood, with the addition of 1 eq. oxygen, and 1 eq. water. Formula of blood .... C 48 N 6 H 39 0 1S 1 eq. water =HO > H 1 O a 1 eq. oxygen = Oj The sum is . . . . — C^^^O' 1 30. If, moreover, we add to the elements of proteine those of 3 eq. water, we obtain, with the exception 1 eq. hydrogen, exactly the same formula. Formula of proteine . . —C«N , H*0 M Add 3 eq. of water . . . — H 3 0 3 The sum is WTO 1 differing only by 1 eq. of hydrogen from the formula above obtained by adding to gether choleic acid and urate of ammonia. 31. If, then, we consider choleic acid and urate of ammonia the products of the transformation of muscular fibre, since no other tissue in the body contains proteine (for albumen passes into tissues, without our being able to say, that in the vital process it is directly resolved into choleic acid, and urate of ammonia,) there exist in fibrine, with the addition of the elements of water, all the elements essential to this metamor URIC ACID AND UREA. 45 phosis; and, except the sulphur and phosphorus, both of which are probably oxidized, no element is separated. This form of metamorphosis is applicable to the vital transformations in the lower classes of amphibia, and perhaps in worms and insects. In the higher classes of animals the uric acid disappears in the urine, and is replaced by urea. The disappearance of uric acid and the production of urea plainly stand in a very close relation to the amount of oxygen absorbed in respiration, and to the quantity of water consumed by different animals in a given time. When uric acid is subjected to the action of oxygen, it is first resolved, as is well known, into alloxan and urea. (32.) A new supply of oxygen acting on the alloxan causes it to resolve itself either into oxalic acid and urea, into oxaluric and parabanic acids, (33,) or into carbonic acid and urea. 32. In the so-called mulberry calculi we find oxalate of lime, in other calculi urate of ammonia, and always in persons, in whom, from want of exercise and labour, or from other causes, the supply of oxygen has been diminished. Calculi containing uric acid or oxalic acid are never found in phthisical patients; and it is a common occurrence in France, among patients suffering from calculous complaints, that when they go to the country, where they take more exercise, the compounds of uric acid, which were deposited in the bladder during their residence in town, are succeeded by oxalates (mulberry calculus,) in consequence of the increased supply of oxygen. With a still greater supply of oxygen they would have yielded, in healthy subjects, only the last product of the oxidation of uric acid, namely, carbonic acid and urea. An erroneous interpretation of the undeniable fact that all substances incapable of farther use in the organism are separated by the kidneys and expelled from the body in the urine, altered or unaltered, has led practical medical men to the idea, that the food, and especially nitrogenized food, may have a direct influence on the formation of urinary calculi. There are no reasons which support this opinion, while those opposed to it are innumerable. It is possible that there may be taken, in the food, a number of matters changed by the culinary art, which, as being no longer adapted to the formation of blood, are expelled in the urine, more or less altered by the respiratory process. But roasting and boiling alter in no way the composition of animal food. (34.) Boiled and roasted flesh is converted at once into blood; while the uric acid and urea are derived from the metamorphosed 5 (C^H^O'^+O 9 "6 atoms hippuric acid, 6 (C 18 P 9 atoms urea . . . 9 (C 2 P ==*l 3 atoms choleic acid . 3 (C 3 *? I 3 atoms ammonia . 8'? P |_3 atoms water . . 3 ( tissues. The quantity of these products increases with the rapidity of transformation in a given time, but bears no proportion to the amount of food taken in the same period. In a starving man who is in any way compelled to undergo severe and continued exertion, more urea is secreted than in the most highly fed individual, if in a state of rest. In fevers and during rapid emaciation the urine contains more urea than in a state of health. (Prout.) 33. In the same way, therefore, as the hippuric acid, present in the urine of the horse when at rest, is converted into benzoate of ammonia and carbonic acid as soon as the animal is compelled to labour, so the uric acid disappears in the urine of man, when he receives, through the skin and lungs, a quantity of oxygen sufficient to oxidize the products of the transformation of the tissues. The use of wine and fat, which are only so far altered in the organism that they combine with oxygen, has a marked influence on the formation of uric acid. The urine, after fat food has been taken, is turbid, and deposits minute crystals of uric acid. (Prout.) The same thing is observed after the use of wines in which the alkali necessary to retain the uric acid in solution is wanting, but never from the use of Rhenish wines, which contain so much tartar. In animals which drink much water, by means of which the sparingly soluble uric acid is kept dissolved, so that the inspired oxygen can act on it, no uric acid is found in the urine, but only urea. In birds, which seldom drink, uric acid predominates. If to one atom of uric acid we add 6 atoms of oxygen and 4 atoms of water, it resolves itself into urea and carbonic acid: 1 atom uric acid C^N 4 !! 4 © 6 4 atoms water £ H 4 0 10 6 atoms oxygen J C'°WH»0 IS < 2 atoms urea - C 4 N 4 H 8 0 4 7 6 atoms carbonic acid C 6 O 12 C M NW« 34. The urine of the herbivora contains no uric acid, but ammonia, urea, and hippuric or benzoic acid. By the addition of 9 atoms of oxygen to the empirical formula of their blood multiplied by 5, we obtain the elements of 6 at. of hippuric acid, 9 at. of urea, 3 at. of choleic acid, 3 at. of water, and 3 at. of ammonia; or, if we suppose 45 atoms of oxygen to be added to the blood during its metamorphoses, then we obtain 6 at. of benzoic acid, 13$ at. of urea, 3 at. of choleic acid, 15 at. of carbonic acid, and 12 at. of water. i) + O 9 = C 240 N 30 H ,95 O 84 6 (C 18 N H* O 5 ) = C ,08 N 6 H^O 30 9 (C 2 N 2 H 4 O 2 ) = C' 8 N^H^O' 8 3 (C M N H M 0 U ) = a^WH 3 NH S )= N 3 H 9 3 ( H 3 O 3 ) = H 3 Q 3 The sum is CPWH'HO" 46 ANIMAL CHEMISTRY. Or— 35. Lastly, let us follow the metamorphosis of the tissues in the fretal calf, considering the proteine furnished in the blood of the mother as the substance which undergoes or has undergone a transformation; it 5 (C 48 N 6 H 39 0 16 ) + O 45 = C 240 N 30 H ,95 O ,2 ° f 6 atoms benzoic acid, 6 (C 14 H 5 O 3 ) = C 84 H^O 18 27I 2 atoms urea . . 27 (C NH 2 O ) m C 27 N 27 H 54 0 27 3 atoms choleic acid 3 = C 114 N 3 H^ 33 15 atoms carbonic acid 15 (C O 2 ) = C 15 O 30 12 atoms water . . 12 ( HO ) = H 12 Q 12 The sum is C^N^H 195 © 120 will appear that 2 at. of proteine without the addition of oxygen or any other foreign element, except 2 at. of water, contain the elements of 6 at. of allantoine and 1 at. of choloidic acid (meconium?) 2 atoms proteine = 2 (C 48 N 6 H 36 0 14 ) + 2 atoms water mi 2H0 = CWH^O 30 _ $ 6 atoms allantoine, 6 (C 4 N 2 H 3 0 3 ) mi C 24 N 12 H 18 0 18 ~" 1 1 atom choloidic acid = C 72 H 56 Q 12 Q96J^12 H 74O30 36. But the elements of the six atoms of exactly to the elements of 2 at. of uric acid, allantoine in the last equation correspond 2 at. of urea, and 2 at. of water. C2 atoms uric acid C 20 N 8 H 8 O 12 6 atoms of allantoine = C 24 N 12 H I8 0 18 = 2 atoms urea C 4 N 4 H 8 0 4 (2 atoms water H 2 0 2 The relations of allantoine, which is found in the urine of the foetal calf, to the nitrogenized constituents of the urine in animals which respire, are, as may be seen by comparing the above formulas, such as cannot be overlooked or doubted. Allantoine contains the elements of uric acid and urea— that is, of the nitrogenized products of the 38. Subtracting from this formula of gelatine the elements of 2 at. of proteine, there remain the elements of urea, uric acid, and C 24 N I2 H 18 0 18 transformation of the compounds of proteine. 37. Further, if to the formula of proteine, multiplied by 3, we add the elements of 4 at. of water, and if we deduct from the sum of all the elements half of the elements of choloidic acid, there remains a formula which expresses very nearly the composition of gelatine. From 3 (CaWEFO 14 ) + 4 HO ... = C 144 N ,8 H n2 0 46 Subtract h atom choloidic acid = C 36 H 28 O 6 There remain .... C 108 N 18 H 84 O 40 (35) water, or of 3 at. of allantoine and 3 at. of water. Thus— Formula of gelatine (Mulder) C^N^H^O 40 Subtract 2 atoms proteine . C 96 N 12 H 72 Q 28 There remain . . . C 12 N 6 H 12 0 12 f 1 atom uric acid C ,0 N 4 H 4 O 6 ") Co « n * • r> nimbus™ —il atom urea . C 2 N 2 H 4 0 2 I « J| a oms WW Q atoms water H 4 Q 4 3 £ 3 atoms water H Q C 12 N 6 H ,2 0 12 C 12 N 6 H 12 0 12 39. The numerical proportions calculated from the above formula differ from those actually obtained in the analyses of Mulder and Sherer in this, that the latter indicate somewhat less of nitrogen in gelatine; but if we assume the formula to be correct, it then appears, from the statement just given, that the elements of two atoms of proteine, plus the nitrogenized products of the transformation of a third atom of proteine (uric acid and urea) and water; or three atoms of proteine, minus the elements of a compound containing no nitrogen, which actually occurs as one of the products of the transformation of choleic acid, yield in both cases a formula closely approaching to the composition of gelatinous tissues. We must, however, attach to such formulae, and to the considerations arising from them, no more importance than justly belongs to them. I would constantly remind the reader that their use is to serve as points of connexion, which may enable us to acquire more accurate views as to the production and decomposition of those compounds which form the animal tissues. They are the first attempts to discover the path which we must follow in order to attain the object of our researches; and this object, the goal we strive to reach, is, and must be, attainable. The experience of all those who have occupied themselves with researches into natural phenomena leads to this general result, that these phenomena are caused or produced, by means far more simple than those previously supposed, or than we even now imagine; and it is precisely their simplicity ORIGIN OF THE BILE. 47 which should most powerfully excite our wonder and admiration. Gelatinous tissue is formed from blood, from compounds of proteine. It may be produced bv the addition, to the elements of proteine, of allantoine and water, or of water, urea, and uric acid ; or by the separation from the elements of proteine of a compound containing no nitrogen. The solution of such problems becomes less difficult, when the problem to be solved, the question 1 to be answered, is matured and clearly put. Every experimental decision of any such question in the negative forms the startingpoint of a new question, the solution of which, when obtained, is the necessary consequence of our having put the first question. 40. In the foregoing sections, no other constituent of the bile, besides choleic acid, has been brought into the calculation; because it alone is known with certainty to contain nitrogen. Now, if it be admitted that its nitrogen is derived from the metamorphosed tissues, it is not improbable that the carbon, and other elements which it contains, are derived from the same source. There cannot be the smallest doubt, that in the carnivora, the constituents of the urine and the bile are derived from the transformation of compounds of proteine; for, except fat, they consume no food but such as contains proteine, or has been formed from that substance. Their food is identical with their blood; and it is a matter of indifference which of the two we select as the starting-point of the chemical developement of the vital metamorphoses. There can be no greater contradiction, with regard to the nutritive process, than to suppose that the nitrogen of the food can pass into the urine as urea, without having previously become part of an organized tissue; for albumen, the only constituent of blood, which, from its amount, ought to be taken into consideration, suffers not the slightest change in passing through the liver or kidneys ; we find it in every part of the body with the same appearance and the same properties. These organs cannot be adapted for the alteration or decomposition of the substance from which all the other organs of the body are to be formed. 41. From the characters of chyle and lymph, it appears with certainty that the soluble parts of the food or of the chyme acquire the form of albumen. Hard-boiled white of egg, boiled or coagulated fibrine, which have again become soluble in the stomach, but have lost their coagulability by the action of air or heat, recover these properties by degrees. In the chyle, the acid reaction of the chyme has already passed into the weak alkaline reaction of the blood; and the chyle, when, after passing through the mesenteric glands, it has reached the thoracic duct, contains albumen coagulable by heat; and, when teft to itself, deposits fibrine. All the compounds of proteine, absorbed dur- ing the passage of the chyme through the intestinal canal, take the form of albumen, which, as the results of incubation in the fowl's egg testify, contains the fundamental elements of all organized tissues, with the exception of iron, which is obtained from other sources. Practical medicine has long ago answered the question, what becomes in man of the compounds of proteine taken in excess, what change is undergone by the superabundant nitrogenized food? The blood-vessels are distended with excess of blood, the other vessels with excess of their fluids, and if the too great supply of food be kept up, and the blood, or other fluids adapted for forming blood, be not applied to their natural purposes, if the soluble matters be not taken up by the proper organs, various gases are disengaged, as in processes of putrefacfaction, the excrements assume an altered quality in colour, smell, &c. Should the fluids in the absorbent and lymphatic vessels undergo a similar decomposition, this is immediately visible in the blood, and the nutritive process then assumes new forms. 42. No one of all these appearances should occur, if the liver and kidneys were capable of effecting the resolution of the superabundant compounds of proteine into urea, uric acid, and bile. All the observations which have been made in reference to the influence of nitrogenized food on the composition of the urine have failed entirely to demonstrate the existence of any direct influence of the kind ; for the phenomena are susceptible of another and a far more simple interpretation, if, along with the food, we consider the mode of life and habits of the individuals who have been the subjects of investigation. Gravel and calculus occur in persons who use very little animal food. Concretions of uric acid have never yet been observed in carnivorous mammalia, living in the wild state,* and among nations which live entirely on flesh, deposits of uric acid concretions in the limbs or in the bladder are utterly unknown. 43. That which must be viewed as an undeniable truth in regard to the origin of the bile, or, more accurately speaking, of choleic acid in the carnivora, cannot hold in regard to all the constituents of the bile secreted by the liver in the herbivora, for with the enormous quantity of bile produced, for example, by the liver of an ox, it is absolutely impossible to suppose that all its carbon is derived from the metamorphosed tissues. Assuming the 59 oz. of dry bile (from 37 lbs. of fresh bile secreted by an ox) to contain the same per centage of nitrogen as choleic acid, (3 - 86 per cent.,) this would amount to nearly 2J oz. of nitrogen; and if this ni- * The occurrence of urate of ammonia in a concretion found in a dog, which was examined by Lassaigne, is to be doubted, unless Lassaigne extracted it himself from the bladder of the animal. 48 ANIMAL CHEMISTRY. trogen proceed from metamorphosed tissues, then, if all the carbon of these tissues passed into the bile, it would yield, at the utmost, a quantity of bile corresponding to 7 - 15 oz. of carbon. This is, however, far below the quantity which, according to observation, is secreted in this class of animals. 44. Other substances, besides compounds of proteine, must inevitably take part in the formation of bile in the organism of the herbivora; and these substances can only be the non-nitrogenized constituents of their food. 45. The sugar of bile of Gmelin (picromel or biline of Berzelius,) which Berzelius considers as the chief constituent of bile, while Demargay assigns that place essentially to choleic acid, burns, when heated in the air, like resin, yields ammoniacal products, and when treated with acids, yields taurine and the products of the decomposition of choleic acid; when acted on by alkalies, it yields ammonia and cholic acid. At all events, the sugar of bile contains nitrogen, and much less oxygen than starch or sugar, but more oxygen than the oily acids. When, in the metamorphosis of sugar of bile or choleic acid by alkalies, we cause the separation of nitrogen, we obtain a crystallized acid, very similar to the oily acids (cholic acid,) and capable of forming with bases salts, which have the general characters of soaps. Nay, we may even consider the chief constituents of the bile, sugar of bile and choleic acid, as compounds of oily acids with organic oxides, like the fat oils, and only differing from these in containing no oxide of glycerule. Choleic acid, for example, may be viewed as a compound of choloidic acid with allantoine and water: Choloid. acid. Allant. Water. Choleic acid. C 72 H 56 0 12 +C 4 N 2 H 3 0 3 +H 7 0 7 =r C 76 N 2 H 66 O i!2 Or as a compound of cholic acid, urea, and water: Cholic acid. Urea. Water. Choleic acid. C«H 60 O 18 +C 2 N 2 H 4 O 2 -f-H 2 O 2 —CWHW 46. If, in point of fact, as can hardly be doubted, the elements of such substances as starch, sugar, &c., take part in the production of bile in the organism of the herbivora, there is nothing opposed to such a view in the composition of the chief constituents of bile, as far as our knowledge at present extends. If starch be the chief agent in this process, it can happen in no other way but this—that, as when it passes into fat, a certain quantity of oxygen is separated from the elements of the starch, which, for the same amount of carbon, (for 72 atoms,) contains five times as much oxygen as choloidic acid. Without the separation of oxygen from the elements of starch, it is impossible to conceive its conversion into bile; and this separation being admitted, its • conversion into a compound intermediate in composition between starch and fat offers no difficulty. 47. Not to render these considerations a mere idle play with formula?, and not to lose sight of our chief object, we observe, therefore, that the consideration of the quantitative proportion of the bile secreted in the herbivora leads to the following conclusions :— The chief constituents of the bile of the J herbivora contain nitrogen, and this nitrogen is derived from compounds of proteine. The bile of this class of animals contains more carbon than corresponds to the quantity of nitrogenized food taken, or to the portion of tissue that has undergone metamorphosis in the vital process. A part of this carbon must, therefore, be derived from the non-nitrogenized parts of the food (starch, sugar, &c.;) and in order to be converted into a nitrogenized constituent of bile, a part of the elements of these bodies must necessarily have combined with a nitrogenized compound derived from a compound of proteine. In reference to this conclusion, it is quite indifferent whether that compound of proteine be derived from the food or from the tissues of the body. 48. It has very lately been stated by A. Ure, that benzoic acid, when administered internally, appears in the urine in the form of hippuric acid. Should this observation be confirmed,* it will acquire great physiological significance, since it would plainly prove that the act of transformation of the tissues in the animal body, under the influence of certain matters taken in the food, assumes a new form with respect to the products which are its result; for hippuric acid contains the elements of lactate of urea, with the addition of those of benzoic acid: 1 at. urea . . C 2 N 2 H 4 0 2 } 1 at. lactic acid . . C 6 H 4 0 4 4S-2 at. benzoic acid . C 28 H 10 O 6 3 2 at. benzoic acid C 36 N 2 H 18Q12 S 2 at. chrystallized hippuric = 2 (C 18 NH 9 0«) 49. If we consider the act of transforma- tion of the tissues in the herbivora as we have done in the carnivora, then the blood of the former must yield, as the last products of the metamorphosis, from all the organs taken together, choleic acid, uric acid, and ammonia (see p. 44;) and if we ascribe to the uric acid an action similar to that of the benzoic acid in Ure's observation—such, namely, that the further transformation, owing to the presence of this acid, assumes another form, the elements of the uric acid being incorporated in the final products—it will appear, for example, that 2 at. of pro- * The analysis of the crystals deposited from the urine on the addition of muriatic acid has not been performed. Besides, the statement of A. Ure, that hippuric acid, dissolved in nitric acid, is reddened by ammonia, is erroneous, and shows that the crystals he obtained must have contained uric acid. SECRETIONS AND EXCRETIONS. 49 teine, with the addition of the elements of 3 at. of uric acid and 2 at. of oxygen, might give rise to the production of hippuric acid and urea. 2 at. proteine, 2 (C^H^O 14 ) = C 06 N M H 72 O ,B 3 at. uric acid, 3 (C 10 N 4 H 4 0 6 ) = C^JN^H^O 13 2 at. oxygen = O 2 Thesumis . . . = C l26 J\ Z4 H 84 0 4S = __ C 6 at. hippuric acid, 6 (C 18 N H 8 0 5 ) = C ,08 i\ 6 H 48 0 30 ~~ l 9 at- urea . . . 9 (C 2 N 2 H 4 0 2 ) =¦ C 18 N^H^O 18 The sum is . ~. '. ', = Que^j^QTs 50. Finally, if we bear in mind, that, in the herbivora, the non-nitrogenized constituents of their food (starch, &c.) must, as we have shown, play an essential part in the formation of the bile; that to their elements must of necessity be added those of a nitrogenized compound, in order to pro- duce the nitrogenized constituents of the bile, the most striking result of the combinations thus suggested is this, that the elements of starch added to those of hippuric acid are equal to the elements of choleic acid, plus, a certain quantity of carbonic acid : 2 at. hippuric acid, 2 (C 18 NH 8 0 s ) _ CPPHW 5 at. starch . . 5 (C 12 H I0 O 10 ) = C 60 H^O 50 2 at. oxygen . . = O 2 The sum is _ C^iNWO 92 _ J 2 at. choleic acid 2 (CTYIW 1 ) — C' f NW I 20 at. carbonic acid 20 (C O 2 ) = C 20 O 40 The sum is . . . . . . = CJN'H^O*"" 51. Now since hippuric acid may be derived, along with urea, from the compounds of proteine, when to the elements of the latter are added those of uric acid (see p. 49;) since, further, uric acid, choleic acid, and ammonia contain the elements of proteine in a proportion almost identical with that of proteine itself (see p. 44;) it is obvious that, if from 5 at. of proteine, with the addition of oxygen and of the elements of water, there be removed the elements of choleic acid and ammonia, the remainder will represent the elements of hippuric acid and of urea; and that if, when this separa- In detail 5 at. proteine ~| f 9 at. choleic acid 15 at. starch II 9 at. urea 12 at. water [ ] 3 at. ammonia 5 at. oxygen J [_60 at. carbonic acid 5 at. proteine, 5 (CWETO 14 ) — C^N^H^O 70 15 at. starch, . 15 (C 12 H 10 O 10 ) — C 180 H ,50 O ,!;0 12 at. water, 12 ( HO ) — H ,2 0 12 5 at. oxygen = O 5 tion occurs, and during the further transformation, the elements of starch be present and enter into the new products, we shall obtain an additional quantity of choleic acid, as well as a certain amount of carbonic acid gas. That is to say — that if the elements of proteine and starch, oxygen and water being also present, undergo transformation together and mutually affect each other, we obtain, as the product of this metamorphosis, urea, choleic acid, ammonia, and carbonic acid, and besides these, no other product whatever. The elements of The sum is . . . . = C 420 N 30 H 342 O 23 ' and— 9 at. choleic acid, 9 (C^NH^O 11 ) = C^WH^O 99 9 at. urea, ... 9 (C 2 N 2 H 4 0 2 ) = C*M? O 19 3 at. ammonia, . 3( NH 5 )= N 3 H 9 60 at. carbonic acid, 60 (C O 2 ) = C 60 O 120 The sum is = c^^H^O 237 The transformation of the compounds of pioteine present in the body is effected by means of the oxygen conveyed by the arterial blood, and if the elements of starch, rendered soluble in the stomach, and thus carried to every part, enter into the newly formed compounds, we have the chief constituents of the animal secretions and excretions ; carbonic acid, the excretion of the lungs, urea and carbonate of ammonia, ex- 7 creted by the kidneys, and choleic acid, secreted by the liver. Nothing, therefore, in the chemical composition of those matters which may be supposed to take a share in these metamorphoses, is opposed to the supposition that a part of the carbon of the non azotized food enters into the composition of the bile. 52. Fat, in the animal body, disappears when the supply of oxygen is abundant. E 50 ANIMAL CHEMISTRY. When that supply is deficient, choleic acid may be converted into hippuric acid, lithofellic acid, (37) and water. Lithofellic acid is known to be the chief constituent of the bezoar stones, which occur in certain herbivorous animals : o . u i • -a n76TVT2U66n22 -» f 2 at. hip. acid C^H^O 10 10 a* tten ° N H H I at. litn. acid C 4 » H"0 8 1U at. oxygen. . at. water . . H' 4 Q 14 C76N2JJ66Q32 C 76 N 2 H 66 0 32 53. For the production of bile in the animal body a certain quantity of soda is, in all circumstances, necessary; without the presence of a compound of sodium no bile can be formed. In the absence of soda, the metamorposis of the tissues composed of proteine can yield only fat and urea. If we suppose fat to be composed according to the empirical formula C n H 10 O, then, by the addition of oxygen and the elements of water, to the elements of proteine, we have the elements of fat, urea, and carbonic acid Proteine. Water. Oxygen. 2 (Cmm^O 1 *) -f 12 HO + 14 O = C^N^H^O 54 = T 6 at. urea . . . = C'W^O 12 =«> Fat = C 66 H^O 6 (.18 at. carbonic acid = C 18 O 36 C^JS^H 84 © 54 The composition of all fats lies between the empirical formulas C n H 10 O and C 12 H ,0 O. If we adopt the latter, then the elements of 2 at. proteine, with the addition of 2 at. oxygen and 12 at. water, will yield 6 at. urea, fat (C^H^O 6 ), and 12 at. carbonic acid. It is worthy of observation, in reference to the production of fat, that the absence of common salt (a compound of sodium which furnishes soda to the animal organism) is favorable to the formation of fat; that the fattening of an animal is rendered impossible, when we add to its food an excess of salt, although short of the quantity required to produce a purgative effect. 54. As a kind of general view of the metamorphoses of the nitrogenized animal secretions, attention may here be very properly directed to the fact, that the nitrogenized products of the transformation of the bile are identical in ultimate composition with the constituents of the urine, if to the latter be added a certain proportion of the elements of water. 1 at. uric acid C ,0 N 4 H 4 O 6 ") 1 at. urea . .. C 2 N 2 H 4 0 2 £ = 22 at. water .. __H 22 0 22 3 C12JX6 H 30Q30 _J3 at. taurine C I8 N s H»O i0 _ 1 3 at. ammonia N 3 H 9 C'WH^O 30 1 at. allantoine C 4 N 2 H s 0 3 ? I at. water . . H 7 0 7 5 C 4 N 2 H io 0 io _ <4 at. taurine C'NH'O 10 I I at. ammonia N H 3 C ? _ r2 /m™ 10 at. water H 10 O 10 f HP&M ) f 2 at. oxalic acid C 4 O 8 1 at. taurine C 4 NH 7 O ,0 =«? 1 at. ammonia NH 3 (4 at. water . . H 4 0 4 C 4 NH 7 0 10 RELATION OF STARCH TO BILE. 51 57. The comparison of the amount of carbon in the bile secreted by an herbivorous animal, with the quantity of carbon of its tissues, or of the nitrogenized constituents of its food, which in consequence of the constant transformations may pass into bile, indicates, as we have just seen, a great difference. The carbon of the bile secreted amounts, at least, to more than five times the quantity of that which could reach the liver in consequence of the change of matter in the body, either from the metamorphosed tissues or from the nitrogenized constituents of the food; and we may regard as well founded the supposition that the non-azotized constituents of the food take a decided share in the production of bile in the herbivora; for neither experience nor observation contradicts this opinion. 58. We have given, in the foregoing paragraphs, the analytical proof, that the nitrogenized products of the transformation of bile, namely, taurine and ammonia, may be formed from all the constituents of the urine, with the exception of urea—that is, from hippuric acid, uric acid,allantoine; and when we bear in mind that, by the mere separation of oxygen and the elements of water, choloidic acid may be formed from starch ; — From 6 at. starch=(C 12 H l0 O 10 )=C 72 H 60 O 60 Subtract 44 at. oxygen ) __ H 4 0 48 4 at. water 5 Remains choloidic acid . . . =C 72 H 56 0 12 ; that, finally, choloidic acid, ammonia, and taurine, if added together, contain the elements of choleic acid; — 1 at. choloidic acid — C 72 H^O 12 1 at. taurine . . . = C 4 N H 7 O 10 1 at. ammonia . . = NH 3 1 at. choleic acid = C 76 N 2 H 66 0 22 ;— if all this be considered, every doubt as to the possibility of these changes is removed. 59. Chemical analysis and the study of the living animal body mutually support each other; and both lead to the conclusion that a certain portion of the carbon of the nonazotized constituents of food (of starch, &c, the elements of respiration) is secreted by the liver in the form of bile; and further, that the nitrogenized products of the transformation of tissues in the herbivora do not, as in the carnivora, reach the kidneys immediately or directly, but that, before their expulsion from the body in the form of urine, they take a share in certain other processes, especially in the formation of the bile. They are conveyed to the liver with the non-azotized constituents of the food; they are returned to the circulation in the form of bile, and are not expelled by the kidneys till they have thus served for the production of the most important of the substances employed in respiration. i 60. When the urine is left to itself, the urea which it contains is converted into carbonate of ammonia; the elements of urea are in such proportion, that by the addition of the elements of water, all its carbon is converted into carbonic acid, and all its nitrogen into ammonia. 1 at. urea C 2 N 2 H 4 0 2 ? 2 at. water H 2 0 2 5 ~~ C 2 N 2 H 6 0 4 ( 2 at. carbonic acid C 2 O 4 ¦"* "l 2 at. ammonia N 2 H 6 C 2 N 2 H 6 0 4 61. Were we able directly to produce taurine and ammonia out of uric acid or allantoine, this might perhaps be considered as an additional proof of the share which has been ascribed to these compounds in the production of bile; it cannot, however, be viewed as any objection to the views above developed on the subject, that, with the means we possess, we have not yet succeeded in effecting these transformations out of the body. Such an objection loses all its force, when we consider that we cannot admit, as proved, the pre-existence of taurine and ammonia in. the bile; nay, that it is not even probable that these compounds, which are only known to us as products of the decomposition of the bile, exist ready formed, as ingredients of that fluid. By the action of muriatic acid on bile, we, in a manner, force its elements to 22 at. water - H^O 16 at. oxygen - - 0 16 j C 18 N 6 H 32 0 42 $4 at. taurine - C 16 i\ 4 H 28 0 4 ° ""Mat. urea - C 2 N 2 H 4 0 2 or— 1 at. theobromine C 18 N 6 H ,0 O 4 ~) 24 at. water - H 24 0 24 £> = 16 at. oxygen - 0 I6 _) • C ,8 J\ 6 H 34 0 44 f 4 at. taurine CWHTO 40 =-?2 at. carbonic acid C 2 O 4 £2 at. ammonia N 2 H 6 C18j\6 H 34Q44 or— 1 at. theobromine C ,8 N 6 H ,0 O 4 } 8 at. water - H 8 0 8 = 14 at. oxygen - 0 14 J C 18 N 6 H 18 0 26 $2 at. taurine C 8 N 2 H 14 0 20 ™11 at. uric acid C'°N 4 H 4 O 6 C 18 N 6 H 18 0 26 88. To see how the action of caffeine, asparagine, theobromine, &c, may be explained, we must call to mind that the chief constituent of the bile contains only 3*8 per cent, of nitrogen, of which only the half, or 1*9 per cent., belongs to the taurine. Bile contains, in its natural state, water and solid matter, in the proportion of 90 parts by weight of the former to 10 of the latter. If we suppose these 10 parts by weight of solid matter to be choleic acid, with 3*87 per cent, of nitrogen, then 100 parts of fresh bile will contain 0-171 parts of nitrogen in .the shape of taurine. Now this quantity is contained in 0-6 parts of caffeine: or grains of caffeine can give to an ounce of bile the nitrogen it contains in the form of taurine. If an infusion of tea contain no more than the of a grain of caffeine, still, if it contribute in point of fact to the formation of bile, the action, even of such a quantity, cannot be looked upon as a nullity. Neither can it be denied that in the case of an excess of nonazotized food and a deficiency of motion, which is required to cause the change of matter in the tissues, and thus to yield the nitrogenized product which enters into the composition of the bile; that in such a condition, the health may be benefited by the use of compounds which are capable of supplying the place of the nitrogenized product produced in the healthy state of the body, and essential to the production of an important element of respiration. In a che- 8 1 mical sense—and it is this alone which the preceding remarks are intended to show— caffeine or theine, asparagine, and theobromine are in virtue of their composition better adapted to this purpose than all other nitrogenized vegetable principles. The action of these substances, in ordinary circumstances, is not obvious, but it unquestionably exists. 89. With respect to the action of the other nitrogenized vegetable principles, such as quinine, or the alkaloids of opium, &c, which manifests itself, not in the processes of secretion, but in phenomena of another kind, physiologists and pathologists entertain no doubt that it is exerted chiefly on the brain and nerves. This action is commonly said to be dynamic—that is, it accelerates, or retards, or alters in some way the phenomena of motion in animal life. If we reflect that this action is exerted by substances which are material, tangible and ponderable; that they disappear in the organism ; that a double dose acts more powerfully than a single one; that, after a time, a fresh dose must be given, if we wish to produce the action a second time; all these considerations, viewed chemically, permit only one form of explanation ; the supposition, namely, that these compounds, by means of their elements, take a share in the formation of new, or the transformation of existing brain and nervous matter. However strange the idea may, at first sight, appear, that the alkaloids of opium or of cinchona bark, the elements of codeine, morphia, quinine, &.c, may be converted into constituents of brain and nervous matter, into organs of vital energy, from which the organic motions of the body derive their origin; that these substances form a constituent of that matter, by the removal of which the seat of intellectual life, of sensation, and of consciousness, is annihilated; it is nevertheless certain, that all these forms of power and activity are most closely dependent, not only on the existence, but also on a certain quality of the substance of the brain, spinal marrow, and nerves; insomuch that all the manifestations of the life or vital energy of these modifications of nervous-matter, which are recognized as the phenomena of motion, sensation, or feeling, assume another form as soon as their composition is altered. The animal organism has produced the brain and nerves out of compounds furnished to it by vegetables; it is the constituents of the food of the animal, which, in consequence of a series of changes, have assumed the properties and the structure which we find in the brain and nerves. 90. If it must be admitted as an undeniable truth, that the substance of the brain and nerves is produced from the elements of vegetable albumen, fibrine and caseine, either alone, or with the aid of the elements of non-azotized food or of the fat formed from the latter, there is nothing absurd in the opinion, that other constituents of vege- 58 ANIMAL CHEMISTRY. tables, intermediate in composition between the fats and the compounds of i proteine, may be applied in the organism to the same purpose. 91. According to the researches of Fremy, the chief constituent of the fat found in the brain is a compound of soda with a peculiar acid, the cerebric acid, which contains, in 100 parts, Carbon 66-7 Hydrogen 106 Nitrogen 2-3 Phosphorus 09 Oxygen 19-5 It is easy to see that the composition of cerebric acid differs entirely, both from that of ordinary fats and of the compounds of proteine. Common fats contain no nitrogen, while the compounds of proteine contain nearly 17 per cent. Leaving the phosphorus out of view, the composition of this acid approaches most nearly to that of choleic acid, although these two compounds are quite distinct. 92. Brain and nervous matter is, at all formed in a manner similar to that in which bile is produced; either by the separation of a highly nitrogenized compound from the elements of blood, or by the combination of a nitrogenized product of the vital process with a non-azotized compound (probably, a fatty body.) All that has been said in the preceding pages on the various possible ways by which the bile might be supposed to be formed, all the conclusions which we attained in regard to the co-operation of azotized and nonazotized elements of food, may be applied with equal justice and equal probability to the formation and production of the nervous substance. We must not forget that, in whatever light we may view the vital operations, the production of nervous matter from blood presupposes a change in the composition and qualities of the constituents of blood. That such a change occurs is as certain as that the existence of the nervous matter cannot be denied. In this sense, we must assume, that from a compound of proteine may be formed a first, second, third, &c, product before a certain number of its elements can become constituents of the nerv- ous matter; and it must be considered as quite certain, that a product of the vital process in a plant, introduced into the blood, will, if its composition be adapted to this purpose, supply the place of the first, second, or third product of the alteration of the compound of proteine. Indeed it cannot be considered merely accidental, that the composition of the most active remedies, namely, the vegetable alkaloids, cannot be shown to be related to that of any constituent of the body, except only the substance of the nerves and brain. All of these con- tain a certain quantity of nitrogen, and, in regard to their composition, they are inter- mediate between the compounds of proteine and the fats. 93. In contradistinction to their chemical character, we find that the substance of the brain exhibits the characters of an acid. It contains far more oxygen than- the organic basis or alkaloids. We observe, that quinine and cinchonine, morphia and codeine, strychnia and brucia, which are, respectively, so nearly alike in composition, if they do not produce absolutely the same effect, yet resemble each other in their action more than those which differ more widely in composition. We find that their energy of action diminishes, as the amount of oxygen they contain increases (as in the case of narcotine,) and that, strictly speaking, no one of them can be entirely replaced by another. There .cannot- be a more decisive proof of the nature of their action than this last fact; it must stand in the closest relation to their composition. If these compounds, in point of fact, are capable of taking a share in the formation or in the alteration of the qualities of brain and nervous matter, their action on the healthy as well as the deceased organism admits of a surprisingly simple explanation. If we are not tempted to deny, that the chief constituent of soup may be applied to a purpose corresponding to its composition in the human body, or that the organic constituent of bones may be so employed in the body of the dog, although that substance (gelantine in both cases) is absolutely incapable of yielding blood ; if, therefore, nitrogenized compounds, totally different from the compounds of proteine, may be employed for purposes corresponding to their composition ; we may thence conclude that a product of vegetable life, also different from proteine, but similar to a constituent of the animal body, may be employed by the organism in the same way and for the same purpose as the natural product, originally formed by the vital energy of the animal organs, and that indeed from a vegetable substance. The time is not long gone by, when we had not the very slightest conception of the cause of the various effects of opium, and when the action of cinchona bark was shrouded in incomprehensible obscurity. Now that we know that these effects are caused by crystallizable compounds, which differ as much in composition as in their action on the system; now that we know the substances to which the medicinal or poisonous energy must be ascribed, it would argue only want of sense to consider the action of these substances inexplicable; and to do so, as many have done, because they act in very minute doses, is as unreasonable as it would be to judge of the sharpness of a razor by its weight. 94. It would serve no purpose to give these considerations a greater extension at present. However hypothetical they may appear, they only deserve attention in so far COMPOSITION OF NERVOUS MATTER. 59 as they point out the way which chemistry pursues, and which she ought not to quit, if she would really be of service to physiology and pathology. The combinations of the chemist relate to the change of matter, forwards and backwards, to the conversion of food into the various tissues and secretions, and to their metamorphosis into lifeless compounds; his investigations ought to tell us what has taken place and what can take place in the body. It is singular that we find medicinal agencies all dependent on certain matters, which differ in composition; and if, by the introduction of a substance, certain abnormal conditions are rendered normal, it will be impossible to reject the opinion, that this phenomenon depends on a change in the composition of the constituents of the diseased organism, a change in which the elements of the remedy take a share; a share similar to that which the vegetable elements of food have taken in the formation of fat, of membranes, of the saliva, of the seminal fluid, &c. Their carbon, hydrogen, or nitrogen, or whatever else belongs to their composition,' are derived from the vegetable organism; and, after all, the action and effects of quinine, morphia, and the vegetable poisons in general, are no hypotheses. 95. Thus, as we may say, in a certain sense, of caffeine, or theine, and asparagine, &c, as well as of the non-azotized elements of food, that they are food for the liver, since they contain the elements, by the presence of which that organ is enabled to perform its functions, so we may consider these nitrogenized compounds, so remarkable for their action on the brain and on the substance of the organs of motion, as elements of food for the organs as yet unknown, which are destined for the metamorphosis of the constituents of the blood into nervous substance and brain. Such organs there must be in the animal body, and if, in the diseased state, an abnormal process of production or transformation of the constituents of cerebral and nervous matter has been established; if, in the organs intended for this purpose, the power of forming that matter out of the constituents of blood, or the power of resisting an abnormal degree of activity in its decomposition or transformation, has been diminished; then, in a chemical sense, there is no objection to the opinion, that substances of a composition analogous to that of nervous or cerebral matter, and, consequently, adapted to form that matter, may be employed, instead of the substances produced from the blood, either to furnish the necessary resistance, or to restore the normal condition. 96. Some physiologists and chemists have expressed doubts of the peculiar and distinct character of cerebric acid, a substance which, from its amount of carbon and hydrogen, and from its external characters, resembles a nitrogenized fatty acid. But a nitrogenized fat, having an acid character, is, in fact, no anomaly. Hippuric acid is in many of its characters very similar to the fatty acids, but is essentially distinguished from them by containing nitrogen. The organic constituents of bile resemble the acid resins in physical characters, and yet contain nitrogen. The organic alkalies are intermediate in their physical characters between the fats and resins, and they all contain nitrogen. A nitrogenized fatty acid is as little improbable as the existence of a nitrogenized resin with the characters of a base. 97. An accurate investigation would probably discover differences in the composition of the brain, spinal marrow and nerves. According to the observations of Valentin, the quality of the cerebral and nervous substance is very rapidly altered from the period of death, and very uncommon precautions would be required for the separation of foreign matters not properly belonging to the substance of the spinal marrow or brain. But, however difficult it may appear, the investigation seems yet to be practicable. We know, in the meantime, that all experience is against the notion of a large amount of carbon and hydrogen in the substance of the brain. The absence of nitrogen as an element of the cerebral and nervous matter, appears, at all events, improbable. This substance, moreover, cannot be classed with ordinary fats, because we find the cerebric acid combined with soda, whereas, all fats are compounds of fatty acids with oxide of glycerule. In regard to the phosphorus of the brain, we can only guess as to the form in which the phosphorus exists. Walchner observed recently that bubbles of spontaneously inflammable phosphuretted hydrogen were disengaged from the trough of a spring in Carlsruhe, on the bottom of which fish had putrefied; and gases containing phosphorus have also been observed among the products of the putrefaction of the brain.* * The curator of the museum,at Geneva gave to M. Leroyer, apothecary, a large quantity of spirit of wine, which had been used for the preservation tf fishes, and which he undertook to purify. He distilled from it a mixture of chloride of calcium and quicklime, and evaporated the residue in the air, over a fire. As soon as the mass had acquired a certain consistence, and a higher temperature, a prodigious quantity of spontaneously inflammable phosphoretted hydrogen was disengaged. (Du.nas, V. 267.) 60 ANIMAL CHEMISTRY. PART III. THE PHENOMENA OF MOTION IN THE ANIMAL ORGANISM. I. It might appear an unprofitable task to add one more to the innumerable forms under which the human intellect has viewed the nature and essence of that peculiar cause which must be considered as the ultimate source of the phenomena which characterize vegetable and animal life, were it not that certain conceptions present themselves as necessary deductions from the views on this subject developed in the introduction to the first part of this work. The following pages will be devoted to a more detailed examination of these deductions. It must be admitted here, that all these conclusions will lose their force and significance, if it can be proved that the cause of vital activity has in its manifestations nothing in common with other known causes which produce motion or change of form and structure in matter. But a comparison of its peculiarities with the modus operandi of these other causes, cannot, at all events, fail to be advantageous, inasmuch as the nature and essence of natural phenomena are recognizable, not by abstraction, but only by comparative observations. If the vital phenomena be considered as manifestations of a peculiar force, then the effects of this force must be regulated by certain laws, which laws may be investigated ; and these laws must be in harmony with the universal laws of resistance and motion, which preserve in their courses the worlds of our own and other systems, and which also determine changes of form and structure in material bodies; altogether independently of the matter in which vital activity appears to reside, or of the form in which vitality is manifested. The vital force in a living animal tissue appears as a cause of growth in the mass, and of resistance to those external agencies which tend to alter the form, structure, and composition of the substance of the tissue in which the vital energy resides. This force further manifests itself as a cause of motion and of change in the form and structure of material substances, by the disturbance and abolition of the state of rest in which those chemical forces exist, by which the elements of the compounds conveyed to the living tissues, in the form of food, are held together. The vital force causes a decomposition of the constituents of food, and destroys the force of attraction which is continually exerted between their molecules; it alters the direction of the chemical forces in such wise, that the elements of the constituents of food arrange themselves in another form, and combine to produce new compounds, either identical in composition with the living tissues, or differing from them; it further changes the direction and force of the attraction of cohesion, destroys the cohesion of the nutritious compounds, and forces the new compounds to assume forms altogether different from those which are the result of the attraction of cohesion when acting freely, that is,, without resistance. The vital force is also manifested as a force of attraction, inasmuch as the new compound produced by the change of form and structure in the food, when it has a composition identical with that of the living tissue, becomes a part of that tissue. Those newly-formed compounds, whose composition differs from that of the living tissue, are removed from the situation in which they are formed, and, in the shape of certain secretions, being carried to other parts of the body, undergo in contact with these a series of analogous changes. The vital force is manifested in the form of resistance, inasmuch as by its presence in the living tissues, their elements acquire the power of withstanding the disturbance and change in their form and composition, which external agencies tend to produce; a power which, simply as chemical compounds, they do not possess. As in the case of other forces, the conception of an unequal intensity of the vital force comprehends not only an unequal capacity for growth in the mass and an unequal power of overcoming chemical resistance, but also an inequality in the amount of that resistance which the parts or constituents of the living tissue oppose to a change in their form and composition, from the action of new external active causes of change; just as the force of cohesion or of affinity is in direct proportion to the resistance which these forces oppose to any external cause, mechanical or chemical, tending to separate the molecules, or the elements of an existing compound. The manifestations of the vital force are dependent on a certain form of the tissue in which it resides, as well as on a fixed composition in the substance of the living tissue. The capacity of growth in a living tissue is determined by the immediate contact with matters adapted to a certain decomposition, or the elements of which are capable of becoming component parts of the tissue in which vitality resides. The phenomenon of growth, or increase in the mass, presupposes that the acting vital force is more powerful that the resistance which the chemical force opposes to the decomposition or transformation of the elements of the food. The manifestations of the vital force are dependent on a certain temperature. Neither in a plant nor in an animal do vital phe- MOTION IN THE ANIMAL ORGANISM. 61 nomena occur when the temperature is lowered to a certain extent. The phenomena of vitality in a living organism diminish in intensity when heat is abstracted, provided the lost heat be not restored by other causes. Deprivation of food soon puts a stop to all manifestations of vitality. The contact of the living tissues with the elements of nutrition is determined in the animal body by a mechanical force produced within the body, which gives to certain organs the power of causing change of place, of producing motion, and of overcoming mechanical resistance. We may communicate motion to a body at rest by means of a number of forces, very different in their manifestations. Thus, a time-piece may be set in motion by a falling weight, (gravitation,) or by a bent spring (elasticity.) Every kind of motion may be produced by the electric or magnetic force, as well as by chemical attraction; while we cannot say, as long as we only consider the manifestation of these forces in the phenomenon or result produced, which of these various causes of change of place has set the body in motion. In the animal organism we are acquainted with only one cause of motion; and this is the same cause which determines the growth of living tissues, and gives them the power of resistance to external agencies j it is the vital force. In order to attain a clear conception of these manifestations of the vital force, so different in form, we must bear in mind, that every knoAvn force is recognized by two conditions of activity, entirely different in the phenomena they offer to the attention of the observer. The force of gravitation inherent in the particles of a stone, gives to them a continual tendency to move towards the centre of the earth. This effect of gravitation becomes inappreciable to the senses when the stone, for example, rests upon a table, the particles of which oppose a resistance to the manifestation of its gravitation. The force of gravity, however, is constantly present, and manifests itself as a pressure on the supporting body; but the stone remains at rest; it has no motion. The manifestation of gravity in the state of rest we call its weight. That which prevents the stone from falling is a resistance produced by the force of attraction, by which the particles of the wood cohere together; a mass of water would not prevent the fall of the stone. If the force which impelled the mass of the stone towards the centre of the earth were greater than the force of cohesion in the particles of the wood, the latter would be overcome ; it would be unable to prevent the fall of the stone. When we remove the support, and with it the force which has prevented the manifestation of the force of gravity, the latter at once appears as the cause of change of place in the stone, which acquires motion, or falls. Resistance is invariably the result of a force in action. According as the stone is allowed to fall during a longer or shorter time, it acquires properties which it had not while at rest; it acquires, for example, the power of overcoming more feebleor more powerful obstacles, or that of communicating motion to bodies in a state of rest. If it fall from a certain height it makes a permanent impression on the spot on which it falls; if it fall from a still greater height (during a longer time) it perforates the table ; its own motion is communicated to a certain number of the particles of the wood which now fall along with the stone itself. The stone, while at rest, possessed none of these properties. The velocity of the,falling body is always the effect of the moving force, and is, ceteris paribus/proportional to the force of gravitation. A body, falling freely, acquires at the end of one second a velocity of 30 feet. The same body, if falling on the moon, would acquire in one second only a velocity of $Vfr m of a foot=l inch, because in the moon the intensity of gravitation (the pressure acting on the body, the moving power) is 360 times smaller. If the pressure continue uniform, the velocity is directly proportional to it; so that, for example, the body falling 360 times slower, will, after 360 seconds, have the same velocity as the other body after one second. Consequently, the effect is proportional, not to the moving force alone, nor to the time alone, but to the pressure multiplied into the time, which is called the momentum of force. In two equal masses the velocity expresses the momentum of force. But under the same pressure a body moves more slowly as its mass is greater; a mass twice as great requires, in order to attain in the same time an equal velocity, twice the pressure; or, under the single pressure, it must continue in motion twice as long. In order, therefore, to have an expression for the whole effect produced, we must multiply the mass into the velocity. This product is called the amount of motion. The amount of motion in a given body must in all cases correspond exactly to the momentum of force. These two, the amount of motion and the momentum of force, are also called simply fvrce ; because we suppose that a less pressure acting, for example, during 10 seconds, is equal to a pressure ten times greater, acting only during one second. The momentum of motion in mechanics signifies the effect of a moving force, without reference to the time (velocity) in which it was manifested. If one man, for example, raises 30 lbs. to a height of 100 feet, and a se F 62 ANIMAL CHEMISTRY. cond one 30 lbs. to a height of 200 feet; then the latter has expended twice as much force as the former. A third who raises 60 lbs. to a height of 50 feet, expends no more force than the first did in raising 30 lbs. to the height of 100 feet. The momentum of motion of the first (30x100) is equal to that of the third (60 x 50) while that of the second (30 X200) is twice as great. Momentum of force and momentum of motion in mechanics are therefore expressions or measures for effects of force, having reference to the velocity attained in a given time, or to a given space; and in this sense may be applied to the effects of all other causes of motion, or of change in form and structure, however great or however small may be the space or the time in which their effects are displayed to the senses. Every force, therefore, exhibits itself in matter either in the form of resistance to external causes of motion, or of change in form and structure; or as a moving force when no resistance is opposed to it; or, finally, in overcoming resistance. One and the same force communicates motion and destroys motion; the former when its manifestations are opposed by no resistance ; the latter, when it puts a stop to the manifestation of some other cause of motion, or of change in form and structure. Equilibrium or rest is that state of activity in which one force or momentum of motion is destroyed by an opposite force or momentum of motion. We observe both these manifestations of activity in that force which gives to the living tissues their peculiar properties. The vital force appears as a moving force or cause of motion when it overcomes the chemical forces (cohesion and affinity) which act between the constituents of food, and when it changes the position or place in which their elements occur; it is manifested as a cause of motion in overcoming the chemical attraction of the constituents of food, and is, further, the cause which compels them to combine in a new arrangement, and to assume new forms. It is plain that a part of the animal body possessed of vitality, which has therefore the power of overcoming resistance, and of giving motion to the elementary particles of the food, by means of the vital force manifested in itself must have a momentum of motion, which is nothing else than the measure of the resulting motion or change in form and structure. We know that this momentum of motion in the vital force, residing in a living part, may be employed in giving motion to bodies at rest, (that is, in causing decomposition, or overcoming resistance,) and if the vital force is analogous in its manifestations to other forces, this momentum of motion must be capable of being conveyed or communicated by matters, which in themselves do not destroy its effect by an opposite manifestation of force. Motion, by whatever cause produced, cannot in itself be annihilated ; it may indeed become inappreciable to the senses, but even when arrested by resistance (by the manifestation of an opposite force J its effect is not annihilated. The falling stone, by means of the amount of motion acquired in its descent, produces an effect when it reaches the table. The impression made on the wood, the velocity communicated by its parts to those of the wood, all this is its effect. If we transfer the conceptions of motion, equilibrium, and resistance, to the chemical forces, which, in their modus operandi, approach to the vital force infinitely nearer than gravitation does, we know with the utmost certainty, that they are active only in the case of immediate contact. We know, also, that the unequal capacity of chemical compounds to offer resistance to external disturbing influences, to those of heat, or of electricity, which tend to separate their particles, as well as their power of overcoming resistance in other compounds (of causing decomposition); that, in a word, the active force in a compound depends on a certain order or arrangement, in which its elementary particles touch each other. The same elements, united in a different order, when in contact with other compounds, exert a most unequal power of offering or overcoming resistance. In one form the force manifested is available (the body is active, an acid, for example); in another not (the body is indifferent, neutral); in a third form, the momentum of force is opposed to that of the first (the body is active, but a base). If we alter the arrangement of the elements, we are able to separate the constituents of a compound by means of another active body; while the same elements, united in their original order, would have opposed an invincible resistance to the action of the decomposing agent. In the same way as two equal inelastic masses, impelled with equal velocity from opposite points, on coming into contact are brought to rest; in the same way, therefore, as two equal and opposite momenta of motion mutually destroy each other; so may the momentum of force in a chemical compound be destroyed in whole or in part by an equal or unequal, and opposite momentum of force in a second compound. But it cannot be annihilated as long as the arrangement of the elementary particles, by which its inherent force was manifested, is not changed. The chemical force of sulphuric acid is present in sulphate of lime as entire as in oil of vitriol. It is not appreciable by the senses; but if the cause be removed which prevented its manifestation, it appears in its full force in the compound in which it properly resides. Thus the force of cohesion in a solid may disappear, to the senses, from the action of a chemical force, (in solution,) or of heat, MOTION IN THE ANIMAL ORGANISM. 63 (in fusion,) without being in reality annihi-, lated or even weakened. If we remove the opposing force or resistance, the force of cohesion appears unchanged in crystallization. By means of the electrical force, or that of heat, we can give the most varied directions to the manifestations of chemical force. By these means we can fix, as it were, the order in which the elementary particles shall unite. Let us remove the cause (heat or electricity) which has turned the balance in favour of the weaker attraction in one direction, and the stronger attraction will show itself continually active in another direction; and if this stronger attraction can overcome the vis inertias of the elementary particles, they will unite in a new form, and a new compound of different properties must be the result. In compounds of this kind, in which, therefore, the free manifestation of the chemical force has been impeded by other forces, a blow, or mechanical friction, or the contact of a substance, the particles of which are in a state of motion (decomposition, transformation,) or any external cause, whose activity is added to the stronger attraction of the elementary particles in another direction, may suffice to give the preponderance to this stronger attraction, to overcome the vis inertia?, to alter the form and structure of the compound, which are the result of foreign causes, and to produce the resolution of the compound into one or more new compounds with altered properties. Transformations, or as they may be called, phenomena of motion, in compounds of this class, may be effected by means of the free and available chemical force of another chemical compound, and that without its manifestation being enfeebled or arrested by resistance. Thus the equilibrium in the attraction between the elements of cane-sugar is destroyed by contact with a very small quantity of sulphuric acid, and it is converted into grape-sugar. In the same way we see the elements of starch, under the same influence, arrange themselves with those of water in a new form, while the sulphuric acid, which has served to produce these transformations, loses nothing of its chemical character. In regard toother substances on which it acts, it remains as active as before, exactly as if it had exerted no sort of influence on the cane-sugar or starch. In contradistinction to the manifestions of the so-called mechanical forces, we have recognized in the chemical forces causes of motion and of change in form and structure, without any observable exhaustion of the force by which these phenomena are produced ; but the origin of the continued manifestation of activity remains still the same; it is the absence of an opposite force (a resistance) capable of neutralizing it or bringing it into the state of equilibrium. As the manifestations of chemical forces (the momentum of force in a chemical compound) seem to depend on a certain order in which the elementary particles are united together, so experience tells us, that the vital phenomena are inseparable from matter; that the manifestations of the vital force in a living part are determined by a certain form of that part, and by a certain arrangement of its elementary particles. If we destroy the form, or alter the composition of the organ, all manifestations of vitality disappear. There is nothing to prevent us from considering the vital force as a peculiar property, which is possessed by certain material bodies, and becomes sensible when their elementary particles are combined in a certain arrangement or form. This supposition takes from the vital phenomena nothing of their wonderful peculiarity; it may therefore be considered as a resting point, from which an investigation into these phenomena, and the laws which regulate them, may be commenced; exactly as we consider the properties and laws of light to be dependent on a certain luminiferous matter, or other, which has no further connexion with the laws ascertained by investigation. Considered under this form, the vital force unites in its manifestations all the peculiarities of chemical forces, and of the not less wonderful cause, which we regard as the ultimate origin of electrical phenomena. The vital force does not act, like the force of gravitation or the magnetic force, at infinite distances, but, like chemical forces, it is active only in the case of immediate contact. It becomes sensible by means of an aggregation of material particles. A. living part acquires, on the above supposition, the capacity of offering and of overcoming resistance, by the combination of its elementary particles in a certain form; and as long as its form and composition are not destroyed by opposing forces, it must retain its energy uninterrupted and unimpaired. When, by the act of manifestation of this energy in a living part, the elements of the food are made to unite in the same form and structure as the living organ possesses, then these elements acquire the same powers. By this combination, the vital force inherent in them is enabled to manifest itself freely, and may be applied in the same way as that of the previously existing tissue. If, now, we bear in mind, that all matters which serve as food to living organisms are compounds of two or more elements, which are kept together by certain chemical forces; if we reflect that in the act of manifestation of force in a living tissue, the elements of the food are made to combine in a new order; —it is quite certain that the momentum of force or of motion in the vital force was more powerful than the chemical attraction existing between the elements of the food.* * The hands of a man, who raises with a rope ANIMAL CHEMISTRY 64 The chemical force which kept the elements together acted as a resistance, which was overcome by the active vital force. Had both forces been equal, no kind of sensible effect would have ensued. Had the chemical force been the stronger, the living part would have undergone a change. If we now suppose that a certain amount of vital force must have been expended in bringing to an equilibrium the chemical force, there must still remain an excess of force, by which the decomposition was effected. This excess constitutes the momentum of force in the living part, by means of which the change was produced; by means of this excess the part acquires a permanent power of causing further decompositions, and of retaining its condition, form, and structure, in opposition to external agencies. We may imagine this excess to be removed, and employed in some other form. This would not of itself endanger the existence of the living part, because the opposing forces would be left in equilibrio; but, by the removal of the excess of force, the part would lose its capacity of growth, its power to cause further decompositions, and its ability to resist external causes of change. If, in this state of equilibrium, oxygen (a chemical agent) should be brought in contact with it, then there would be no resistance to the tendency of the oxygen to combine with some element of the living part, because its power of resistance has been taken away by some other application of its excess of vital force. According to the amount of oxygen brought to it, a certain proportion of the living part would lose its condition of vitality, and take the form of a chemical combination, having a composition different from that of the living tissue. In a word, there would occur a change in the properties of the living compound, or what we have called a change of matter. If we reflect that the capacity of growth or increase of mass in plants is almost unlimited ; that a hundred twigs from a willow tree, if placed in the soil, become a hundred trees; we can hardly entertain a doubt, that with the combination of the elements of the food of the plant so as to form a part of it, a fresh momentum of force is added in the newly* formed part to the previously existing momentum in the plant; insomuch, that with the increase of mass, the sum of vital force is augmented. According to the amount of available vital force, the products formed by its activity from the food are varied. The composition and simple pulley, 30 lbs. to the height of 100 feet, pass over a space of 100 feet, while his muscular energy furnishes the equilibrium to a pressure of 30 lbs. Were the force which the man could exert not greater than would suffice to keep in equilibrium a pressure of 30 lbs., he would be unable to raise the weight to the height mentioned. of the buds, of the radical fibres, of the leaf, of the flower, and of the fruit, are very different one from the other; and the chemical force by which their elements are held together is very different in each of these cases. Of the tion-azotized constituents of plants we may assert, that no part|>f the momentum of force is expendedln maintaining their form and structure, when their elements have once combined in that order in which they become parts of organs endued with vitality. Very different is the character of the azotized vegetable principles; for, when separated from the plant, they pass, as is commonly said, spontaneously, into fermentation and putrefaction. The cause of this decomposition or transformation of their elements is the chemical action which the oxygen of the atmosphere exercises on one of their constituents. Now we know, that as long as the plant exhibits the phenomena of life, oxygen gas is given oft'from its surface ; that this oxygen is altogether without action on the constituents of the living plant, for which, in other circumstances, it has the strongest attraction. It is obvious, therefore, that a certain amount of vital force must be expended, partly to retain the elements of the complex azotized principles in the form, order, and structure which belong to them; and partly as a means of resistance against the incessant tendency of the oxygen of the atmosphere to act on their elements, as well as against that of the oxygen separated in the organism of the plant by the vital process. With the increase of these easily altered compounds, in the flower and in the fruit, for example, the sum of chemical force (the free manifestation of which, counteracted by an equal measure of vital force, is employed to furnish resistance) also increases. The plant increases in mass until the vital force inherent in it conies into equilibrium with all the other causes opposed to its manifestation. From this period, every new cause of disturbance, added to those previously existing (a change of temperature, for example,) deprives it of the power of offering resistance, and it dies down. In perennial plants (in tyees, for example,) the mass of the easily decomposable (azotized) compounds, compared with that of the non-azotized, is so small, that of the whole sum of force, only a minimum is expended as resistance. In animals, this proportion is reversed. During every period of the life of a plant, the available vital force (that which is not neutralized by resistance) is expended only in one form of vital manifestation, that of growth or increase of mass, or the overcoming of resistance. No part of this force is applied to other purposes. In the animal organism, the vital force exhibits itself, as in the plant, in the form of the capacity of growth, and as the means of resistance to external agencies; but both MOTION IN THE ANIMAL ORGANISM. 65 of these manifestations are confined within certain limits. We observe in animals, that the conversion of food into blood, and the contact of the blood with the living tissues, are determined by a mechanical force, whose manifestation proceeds from distinct organs, and is effected by a distinct system of organs, possessing the property of communicating and extending the motion which they receive. We find the power of the animal to change its place and to produce mechanical effects by means of its limbs, dependent on a second similar system of organs or apparatus. Both of these systems of apparatus, as well as the phenomena of motion proceeding from them, are wanting in plants. In order to form a clear conception of the origin and source of the mechanical motions in the animal body, it may be advantageous to reflect on the modus operandi of other forces, which in their manifestations are most closely allied to the vital force. When a number of plates of zinc and copper, arranged in a certain order, are brought into contact with an acid, and when the extremities of the apparatus are joined by means of a metallic wire, a chemical action begins at the surface of the plates ol zinc, and the wire, in consequence of this action, acquires the most singular and wonderful properties. The wire appears as the carrier or con* ductor of a force, which may be conducted and communicated through it in every direction with amazing velocity. It is the conductor or propagator of an uninterrupted series of manifestations of activity. Such a propagation of motion is inconceivable, if in the wire there were a resistance to be overcome; for every resistance would convert a part of the moving force into a force at rest. When the wire is divided in the middle, and its continuity interrupted, the propagation of force ceases, and we observe, that in this case the action between the zinc and the acid is immediately stopped. If the communication be restored, the action which had disappeared reappears with all its original energy. By means of the force present in the wire, we can produce the most varied effects ; we can overcome all kinds of resistance, raise weights, set ships in motion, &c. And, what is still more remarkable, the wire acts as a hollow tube, in which a current of chemical force circulates freely and without hindrance. Those properties which, when firmly attached to certain bodies, we call the strongest and most energetic affinities, we find, to all appearance, free and uncombined in the wire. We can transport them from the wire to other bodies, and thereby give to them an affinity (a power of entering into combination) which in themselves they do not possess. According to the amount of force circulating in the wire, we are able by 9 means of it to decompose compounds, the elements of which have the strongest attraction for each other. Yet the substance of the wire takes not the smallest share in all these manifestations of force ; it is merely the conductor of force. We observe, further, in this wire, phenomena of attraction and repulsion, which we must ascribe to the disturbance of the equilibrium in the electric or magnetic force; and when this equilibrium is restored, the restoration is accompanied by the developement of light and heat, its never-failing companions. All these remarkable phenomena are produced by the chemical action which the zinc and the acid exert on each other; they are accompanied by a change in form and structure, which both undergo. The acid loses its chemical character; the zinc enters into combination with it. The manifestations of force produced in the wire are the immediate consequence of the change in the properties of the acid and the metal. . - One particle of acid after another loses its peculiar chemical character; and we perceive that in the same proportion the wire acquires a chemical, mechanical, galvanic, or magnetic force, whatever name be given to it. According to the number of acid particles which in a given time undergo this change, that is, according to the surface of the zinc, the wire receives a greater or less amount of these forces. The continuance of the current of force depends on the duration of the chemical action ; and the duration of the latter is most closely connected with the carrying away, by conduction, of the force. If we check the propagation of the current of force, the acid retains its chemical character. If we employ it to overcome chemical or mechanical resistance, to decompose chemical compounds, or to produce motion, the chemical action continues; that is to say, one particle of acid after another changes its properties. In the preceding paragraphs we have considered these remarkable phenomena in a form which is independent of the explanations of the schools. Is the force which circulates in the wire the electrical force? Is it chemical affinity? Is it propagated in the conductor like a fluid set in motion, or in the form of a series of momenta of motion, like light and sound, from one particle of the conductor to another ? All this we know not, and we shall never know. All the suppositions which may be employed as explanations of the phenomena have not the slightest influence on the truth of these phenomena; for they refer merely to the form in which they are manifested. On some points, however, there is no doubt; namely, that all the effects which may be produced by the wire are determined by the change of properties in the zinc and in the acid; for the term " chemi- r* 66 ANIMAL CHEMISTRY. cal action" signifies neither more nor less than the act of change in them; that these effects depend on the presence of a conductor, of a substance which propagates in all directions, where it is not neutralized by resistance, the force or momentum produced ; that this force. becomes a momentum of motion, by means of which we can produce mechanical effects, and which, when transferred to other bodies, communicates to them all those properties, the ultimate cause of which is the chemical force itself; for these bodies acquire the power of causing decompositions and combinations, such as, without a supply of force through the conductor, they could not effect. If we employ these well known facts as means to assist us in investigating the ultimate cause of the mechanical effects in the animal organism, observation teaches us, that the motion of the blood and of the other animal fluids proceeds from distinct organs which, as in the case of the heart and intestines, do not generate the moving power in themselves, but receive it from other quarters. We know with certainty that the nerves are the conductors and propagators of mechanical effects; we know, that by means of them motion is propagated in all directions. For each motion we recognize a separate nerve, a peculiar conductor, with the conducting power of which, or with its interruption, the propagation of motion is affected or destroyed. By means of the nerves all parts of the body, all the limbs, receive the moving force which is indispensable to their functions, to change of place, to the production of mechanical effects. Where nerves are not found, motion does not occur. The excess of force generated in one place is conducted to other parts by the nerves. The force which one organ cannot produce in itself is conveyed to it from other quarters; and the vital force which is wanting to it, in order to furnish resistance to external causes of disturbance, it receives in the form of excess from another organ, an excess which that organ cannot consume in itself. We observe further, that the voluntary and involuntary motions, in other words, all mechanical effects in the animal organism, are accompanied by, nay, are dependent on, a peculiar change of form and structure in the substance of certain living parts, the increase or diminution of which change stands in the very closest relation to the measure of motion, or the amount of force consumed in the motions performed. As an immediate effect of the manifestation of mechanical force, we see, that a part of the muscular substance loses its vital properties, its character of life; that this {>ortion separates from the living part, and 06es its capacity of growth and its power of resistance. We find that this change of properties is accompanied by the entrance of a foreign body (oxygen) into the composi- tion of the muscular fibre (just as the acid lost its chemical character by combining with zinc ;) and all experience proves, that this conversion of living muscular fibre into compounds destitute of vitality is accelerated or retarded according to the amount of force employed to produce motion. Nay, it may safely be affirmed, that they are mutually proportional; that a rapid transformation of muscular fibre, or, as it may be called, a rapid change of matter, determines a greater amount of mechanical force; and conversely, that a greater amount of mechanical motion (of mechanical force expended in motion) determines a more rapid change of matter. From this decided relation between the change of matter in the animal body and the force consumed in mechanical motion, no other conclusion can be drawn but this, that the active or available vital force in certain living parts is the cause of the mechanical phenomena in the animal organism. The moving force certainly proceeds from living parts; these parts possessed a momentum of force or of motion, which they lost in proportion as other parts acquired, a momentum of force or of motion; they lose their capacity of growth, and their power to resist external causes of change. It is obvious that the ultimate cause, the vital force, from which they acquired these properties, has served for the production of mechanical force, that is, has been expended in the shape of motion. How, indeed, could we conceive that a living part should lose the condition of life, should become incapable of resisting the action of the oxygen conveyed to it by the aiterial blood, and should be deprived of the power to overcome chemical resistance, unless the momentum of the vital force, which had giyen to it all these properties, had been expended for other purposes'? By the power of the conductors, the nerves to propagate the momentum of force in a living part, or the effect which the active vital force inherent in the part pro» duces on all the surrounding parts, in all directions where the force, or rather its momentum of motion, is consumed without resistance, (for without motion no change of matter occurs, and when motion has begun, there is no longer resistance,) an equilibrium is obviously established in the living part, between the chemical forces and the remaining vital force; which equilibrium would not have occurred had not vital force been expended in producing me-' chanical motion. In this state, any external cause capable of exerting an influence on the form, structure and composition of the organ meets with no further resistance. If oxygen were not conveyed to it, the organ would maintain its condition, but without, any manifestation of vitality. It is only with the commencement of chemical action that the change of matter, that is, the separation of MOTION IN THE ANIMAL ORGANISM. 67 a part of the organ in the form of lifeless compounds, begins. The change of matter, the manfestation of mechanical force, and the absorption of oxygen, are, in the animal body, so closely connected with each other, that we may consider the amount of motion, and the quantity of living tissue transformed, as proportional to the quantity of oxygen inspired and consumed in a given time by the animal. For a certain amount of motion, for a certain proportion of vital force consumed as mechanical force, an equivalent of chemical force is manifested; that is, an equivalent of oxygen enters into combination with the substance of the organ which has lost the vital force; and a corresponding proportion of the substance of the organ is separated from the living tissue in the shape of an oxidized compound. All those parts of the body which nature has destined to effect the change of matter, that is, to the production of mechanical force, are penetrated in all directions by a multitude of the most minute tubes or vessels, in which a current of oxygen continually circulates, in the form of arterial blood. To the above-mentioned separation of part of the elements of these parts, in other words, to the disturbance of their equilibrium, this oxygen is absolutely essential. As long as the vital force of these parts is not conducted away and applied to other purposes, the oxygen of the arterial blood has not the slightest effect on the substance of the organized parts; and in all cases, only so much oxygen is taken up as corresponds to the conducting power, and, consequently to the mechanical effects produced. The oxygen of the atmosphere is the proper, active, external cause of the waste of matter in the animal body; it acts like a force which disturbs and tends to destroy the manifestation of the vital force at every moment. But its effect as a chemical agent, the disturbance proceeding from it, is held in equilibrium by the vital force, which is free and available in the living tissue, or is annihilated by a chemical agency opposed to that of oxygen, the manifestation of which must be considered as dependent on the vital force. In chemical language, to annihilate the chemical action of oxygen, means, to present to it substances, or parts of organs, which are capable of combining with it. The action of oxygen (affinity) is either neutralized by means of the elements of organized parts, which combine with it, (after the free vital force has been conducted away,) or else the organ presents to it the products of other organs, or certain matters formed from the elements of the food, by the vital activity of certain systems of apparatus. It is only the muscular system which, in this sense, produces in itself a resistance to the chemical action of oxygen, and neutralizes it completely. The substance of cellular tissue, of membranes, and of the skin, the minutest particles of which are not in immediate contact with arterial blood, (with oxygen,) are not destined to undergo this change of matter. Whatever changes they may undergo in the vital process, affect, in all cases, only their surface. The gelatinous tissues, mucous membranes, tendons, &c, are not designed to produce mechanical force; they contain in their substance no conductors of mechanical effects. But the muscular system is interwoven with innumerable nerves. The substance of the uterus is in no respect different in chemical composition from the other muscles ; but it is not adapted to the change of matter, to the production of force, and contains no organs for conducting away the moving power. Cellular tissue, gelatinous membranes, and mucous membranes, are far from being destitute of the power of combining with oxygen, when moisture is present; we know that, when moist, they cannot be brought in contact with oxygen without undergoing a progressive alteration. But one surface of the intestines and the cells of the lungs are constantly in contact with oxygen; and it is obvious that they must be as rapidly altered by the chemical action of the oxygen in the body as out of it, were it not that there exists in the organism itself a source of resistance, which completely neutralizes the action of the oxygen. Among the means by which this resistance is furnished we may include all substances which are capable of combining with oxygen, or acquire that property under the influence of the vital force, and which surpass the tissues above mentioned in their power of neutralizing its chemical action. All those constituents of the body which, in themselves, do not possess, in the form of vital force, the power of resisting the action of oxygen, must be far better adapted for the purpose of combining with, and neutralizing it, than those tissues which are under the influence of the vital force, although only through the nerves. In this point of view, we cannot fail to perceive the importance of the bile in regard to the substance of the intestines, and that of the pulmonary cells, as well as that of fat, of mucus, and of the secretions generally. When the membranes are compelled from their own substance to furnish resistance to the action of the oxygen, that is, when there is a deficiency of the substances destined by nature for their protection, they must, since their renewal is confined within narrow limits, yield to the chemical action. The lungs and intestines will always simultaneously suffer abormal changes. From the change of matter itself, from the metamorphosis of the living muscular tissue, these organs receive the means of resistance to the action of oxygen which are indispensable to their preservation. According to the rapidity of this process, the quan- 68 ANIMAL CHEMISTRY. tity of bile secreted increases; while that of the fat present in the body diminishes in the same proportion. For carrying on the involuntary motions in the animal body, a certain amount of vital force is expended at every moment of its existence; and, consequently, an incessant change of matter goes on; but the amount of living tissue, which, in consequence of this form of consumption of vital force, loses its condition of life and its capacity of growth, is confined within narrow limits. It is directly proportional to the force required for these involuntary motions. Now, although we may suppose that the living muscular tissue, with a sufficient supply of food, never loses its capacity of growth; that this form of vital manifestation is continually effective; this cannot apply to those parts of the body whose available vital force has been expended in producing mechanical effects. For the waste of matter, in consequence of motion and laborious exertion, is extremely various in different individuals. If Ave reflect, that the slightest motion of a finger consumes force; that in consequence of the force expended, a corresponding portion of muscle diminishes in volume; it is obvious, that an equilibrium between supply and waste of matter (in living tissues) can only occur when the portion separated or expelled in a lifeless form is, at the same instant in which it loses its vital condition, restored in another part. The capacity of growth or increase in mass depends on the momentum of force belonging to each part; and must be capable of continued manifestation (if there be a sufficient supply of nourishment,) as long as it does not lose this momentum, by expending it, for example, in producing motion. In all circumstances, the growth itself is restricted to the time: that is to say, it cannot be unlimited in a limited time. A living part cannot increase in volume at the same moment in which a portion of it loses the vital condition, and is expelled from the organ in the form of a lifeless compound; on the contrary, its volume must diminish. The continued application of the momentum of force in living tissues to mechanical effects determines, therefore, a continued separation of matter; and only from the period at which the cause of waste ceases to operate, can the capacity of growth be manifested. Now, since, in different individuals, according to the amount of force consumed in producing voluntary mechanical effects, unequal quantities of living tissue are wasted, there must occur, in every individual, unless the phenomena of motion are to cease entirely, a condition in which all voluntary motions are completely checked, in which, therefore, these occasion no waste. This condition is called sleep. The growth of one part, which is not de- prived of its vital force, cannot be in the slightest degree affected by the consumption of the vital force of another part in producing motion. The one may increase in volume, while the other diminishes; and the waste in one can neither increase nor diminish the supply in the other. Now, since the consumption of force for the involuntary motions continues in sleep, it is plain that a waste of matter also continues in that state; and if the original equilibrium is to be restored, we must suppose that, during sleep, an amount of force is accumulated in the form of living tissue, exactly equal to that which was consumed in voluntary and involuntary motion during the preceding waking period. If the equilibrium between waste and supply of matter be in the least degree disturbed, this is instantly seen in the different amount of force available for mechanical purposes. It is further obvious, that if there should occur a disproportion between the conducting power of the nerves of voluntary and involuntary motion, a difference in the phenomena of motion themselves will be perceptible, in the same proportion as the one or the other is capable of propagating the momentum offeree, generated by the change of matter. As the motions of the circulating system and of the intestines increase, the power of producing mechanical effects in the limbs must diminish in the same proportion (as in wasting fevers;) and if, in a given time, more vital force has been consumed for mechanical purposes (labour, running, dancing, &c.,) than is properly available for the voluntary and involuntary motions; if force be expended more rapidly than the change of matter can be effected in the same time; then a part of that force which is necessary for the involuntary motions must be expended in restoring the excess of force consumed in voluntary motion. The motions of the heart and of the intestines, in this case, will be retarded, or will entirely cease. From the unequal degree of conducting power in the nerves, we must deduce those conditions which are termed paralysis, syncope, and spasm. Paralysis of the nerves of voluntary motion may exist without emaciation; but frequently recurring attacks of epilepsy (in which vital force is rapidly wasted in producing mechanical effects) are always accompanied by remarkably rapid emaciation. It ought to excite the highest admiration when we consider with what infinite wisdom the Creator has divided the means by which animals and plants are qualified for their functions, for their peculiar vital manifestations. The living part of a plant requires the whole force and direction of its vital energy from the absence of all conductors of force. By this means the leaf is enabled to overcome the strongest chemical attractions, to MOTION OF ANIMAL ORGANISM. 69 decompose carbonic acid, and to assimilate the elements of its nourishment. In the flower alone does a process similar to the change of matter in the animal body occur. There, phenomena of motion appear ; but the mechanical effects are not propagated to a distance, owing to the absence of conductors of force. The same vital force which we recognize in the plant as an almost unlimited capacity of growth, is converted in the animal body into moving power (into a current of vital force;) and a most wonderful and wise economy has destined for the nourishment of the animal only such compounds as have a composition identical with that of the organs which generate force, that is, with the muscular tissue. The expenditure of force which the living parts of animals require, in order to reproduce themselves from the blood; the resistance of the chemical force which has to be overcome in the azotized constituents of food by the vital agency of the organs destined to convert them into blood; these are as nothing compared to the force with which the elements of carbonic acid are held together. A certain amount of force would necessarily be prevented from assuming the form of moving power, if it were to be expended in overcoming chemical resistance; for the momentum of motion of the vital force is diminished by all obstacles. But the conversion of the constituents of blood into muscular fibre (into an organ which generates force) is only a change of form. Both have the same composition; blood is fluid, muscular fibre is solid blood. We may even suppose that this change takes piace without any expenditure of vital force ; for the mere passage of a fluid body into the solid state requires no manifestation of force, but only the removal of obstacles, which oppose that force (cohesion) which determines the form of matter, in its manifestations, w In what form or in what manner the vital force produces mechanical effects in the animal body is altogether unknown, and is as little to be ascertained by experiment as the connexion of chemical action with the phenomena of motion which we can produce with the galvanic battery. All the explanations which have been attempted are only representations of the phenomenon; they are, more or less, exact descriptions and comparisons of known phenomena with these, whose cause is unknown. In this respect we are like an ignorant man, to whom the rise and fall of an iron rod in a cylinder, in which the eye can perceive nothing, and its connexion with the turning and motion of a thousand wheels at a distance from the piston-rod, appear incomprehensible. We know not how a certain something, invisible and imponderable in itself (heat) gives to certain bodies the power of exerting an enormous pressure on surrounding objects; we knqw not even how this something itself is produced when we burn wood or coals. So is it with the vital force, and with the phenomena exhibited by living bodies. The cause of these phenomena is not chemical force; it is not electricity, nor magnetism; it is a force which has certain properties in common with all causes of motion and of change in form and structure in material substances. It is a peculiar force, because it exhibits manifestations which are found in no other known force. II. In the living plant, the intensity of the vital force far exceeds that of the chemical action of oxygen. We know, with the utmost certainty, that by the influence of the vital force, oxygen is separated from elements to which it has the strongest affinity ; that it is given out in the gaseous form, without exerting the slightest action on the juices of the plant. How powerful, indeed, must the resistance appear which the vital force supplies to leaves charged with oil of turpentine or tannic acid, when we consider the affinity of oxygen for these compounds! This intensity of action or of resistance the plant obtains by means of the sun's light; the effect of which in chemical actions may be, and is, compared to that of a very high temperature (moderate red heat.) During the night an opposite process goes on in the plant; we see then that the constituents of the leaves and green parts combine with the oxygen of the air, a property which in daylight they did not possess. From these facts we can draw no other conclusion but this : that the intensity of the vital force diminishes with the abstraction of light; that with the approach of night a state of equilibrium is established, and that in complete darkness all those constituents of plants which, during the day, possessed the power of separating oxygen from chemical combinations, and of resisting its action, lose their power completely. A precisely similar phenomenon is observed in animals. The living animal body exhibits its peculiar manifestations of vitality only at certain temperatures. When exposed to a certain degree of cold, these vital phenomena entirely cease. The abstraction of heat must, therefore, be viewed as quite equivalent to a diminution of the vital energy; the resistance opposed by the vital force to external causes of disturbance must diminish, in certain temperatures, in the same ratio in which the tendency of the elements of the body to combine with the oxygen of the air increases. By the combination of oxygen with the constituents of the metamorphosed tissues, the temperature necessary to the manifestations of vitality is produced in the carnivora. In the herbivora, again, a certain amount of heat is developed by means of those elements of their non-azotized food which have the property of combining with oxygen. It is obvious that the temperature of an 70 ANIMAL CHEMISTRY. animal body cannot change, if the amount of inspired oxygen increases in the same ratio as the loss of heat by external cooling. Two individuals, carnivora, of equal weight, exposed to unequal degrees of cold, lose, in a given time, by external cooling, unequal quantities of heat. Experience teaches, that if their peculiar temperature and their original weight are to remain unaltered, they require unequal quantities of food; more in the lower temperature than in the higher. The circumstance that the original weight remains the same, with unequal quantities of food, obviously presupposes, that in the same time a quantity of oxygen proportioned to the temperature has been absorbed; more in the lower than in the higher temperature. We find that the weight of both individuals, at the end of 24 hours, is equal to the original weight. But we have assumed that their food is converted into blood; that the blood has served for nutrition; and it is plain, that when the original weight has been restored, a quantity of the constituents of the body, equal in weight to those of the food, has lost its condition of life, and has been expelled in combination with oxygen. The one individual, which, being exposed to the lower temperature, consumed more food, has also absorbed more oxygen; a greater quantity of the constituents of its body has been separated in combination with oxygen; and, in consequence of this combination with oxygen, a greater amount of heat has been liberated, by which means the heat abstracted has been restored, and the proper temperature of the body kept up. Consequently, by the abstraction of heat, provided there be a full supply of food and free access of oxygen, the change of matter must be accelerated; and, along with the augmented transformation, in a given time, of living tissues, a' greater amount of vital force must be rendered available for mechanical purposes. With the external cooling, the respiratory motions become stronger; in a lower temperature more oxygen is conveyed to the blood; the waste of matter increases, and if the supply be not kept in equilibrium with this waste, by means of food, the temperature of the body gradually sinks. But, in a given time, an unlimited supply of oxygen cannot be introduced into the body; onlv a certain amount of living tissue can lose the state of life, and only a limited amount of vital force can be manifested in mechanical phenomena. It is only, therefore, when the cooling, the generation of force, and the absorption of oxygen are in equilibrium together, that the temperature of the body can remain unchanged. If the loss of heat bv cooling go beyond a certain point, the vital phenomena diminish in the same ratio; for the temperature falls, and the temperature must be considered as a uniform condition of their manifestation. Now experience teaches, that when the temperature of the body sinks, the power of the limbs to produce mechanical effects (or the force necessary to the voluntary motions) is also diminished. The condition of sleep ensues, and at last even the involuntary motions (those of the heart and intestines, for example) cease, and apparent death or syncope supervenes. It is obvious that the cause of the generation of force, namely, the change of matter, is diminished, because, with the abstraction of heat, as in the plant by abstraction of light, the intensity of the vital force diminishes. It is also obvious that the momentum of force in a living part depends on its proper temperature; exactly as the effect of a falling body stands in a fixed relation to certain other conditions; for example, to the velocity attained in falling. When the temperature sinks, the vital energy diminishes; when it again rises, the momentum of force in the living parts appears once more in all its original intensity. The production of force for mechanical purposes, and the temperature of the body, must, consequently, bear a fixed relation to the amount of oxygen which can be absorbed in a given time by the animal body. The quantities of oxygen which a whale and a carrier's horse can inspire in a given time are very unequal. The temperature, as well as the quantity of oxygen, is much greater in the horse. The force exerted by a whale, when struck with the harpoon, his body being supported by the surroundinsr medium, and the force exerted by a carrier's horse, which carries its own weight and a heavy burden for eight or ten hours, must both bear the same ratio to the oxygen consumed. If we take into consideration the time during which the force is manifested, it is obvious that the amount of forc£ developed by the horse is far greater tharPin the case of the whale. In climbing high mountains, where, in consequence of the respiration of a highly rarefied atmosphere, much less oxygen is conveyed to the blood, in equal times, than in valleys or at the level of the sea, the change of matter diminishes in the same ratio, and with it the amount of force available for mechanical purposes. For the most part, drowsiness and want of force for mechanical exertions come on; after twenty or thirty steps, fatigue compels us to a fresh accumulation of force by means of rest (absorption of oxygen without waste of force in voluntary motions.) By the absorption of oxygen into the'substance of living tissues, these lose their condition of life, and are separated as lifeless, unorganized compounds; but the whole of the inspired oxygen is not applied to these transformations: the greater part serves to convert into gas and vapour all matters which no longer belong to the organism; and, as formerly mentioned, the combina - tion of the elements of such compounds MOTION IN THE ANIMAL ORGANISM. 71 with the oxygen produces -the temperature proper to the animal organram. The production of heat and the change of matter are closely related to each other: but although heat can be produced in the body without any change of matter in living tissues, yet the change of matter cannot be supposed to take place without the co-operation of oxygen. According to all the observations hitherto made, neither the expired* air nor the perspiration, nor the urine, contains any trace of alcohol, after indulgence in spirituous liquors; and there can be no doubt that the elements of alcohol combine with oxygen in the body; that its carbon and hydrogen are given off as carbonic acid and water. The oxygen which has accomplished this change must have been taken from the arterial blood; for we know of no channel, save the circulation of the blood, by which oxygen can penetrate into the interior of the body. Owing to its volatility, and the ease with which its vapour permeates animal membranes and tissues, alcohol can spread throughout the body in all directions. If the power of the elements of alcohol to combine with oxygen were not greater than that of the compounds formed by the change of matter, or that of the substance of living tissues, they (the elements of alcohol) could not combine with oxygen in the body. It is, consequently, obvious, that by the use of alcohol a limit must rapidly be put to the change of matter in certain parts of the body. The oxygen of the arterial blood, which, in the absence of alcohol, would have combined with the matter of the tissues, or with that formed by the metamorphosis of these tissues, now combines with the elements of. alcohol. The arterial blood becomes venous, without the substance of the muscles having taken any share in the transformation. Now we observe, that the developement of heat in the body, after the use of wine, increases rather than diminishes, without the manifestation of a corresponding amount of mechanical force. A moderate quantity of wine, in women and children unaccustomed to its use, produces, on the contrary, a diminution of the force necessary for voluntary motions. Weariness, feebleness in the limbs, and drowsiness, plainly show that the force available for mechanical purposes, in other words, the change of matter, has been diminished. A diminution of the conducting power of the nerves of voluntary motion may doubtless take a certain share in producing these symptoms; but this must be altogether without influence on the sum of available force. What the conductors of voluntary motion cannot carry away for effects of force, must be taken up by the nerves of involuntary motion, and conveyed to the heart, lungs, and intestines. In this case, the circulation will appear accelerated at the expense of the force available for voluntary motion; but, as was before remarked, without the production of a greater amount of mechanical force by the process of oxidation of the alcohol. Finally, we observe, in hybernating animals, that, during their winter sleep, the capacity of increase in mass (one of the chief manifestations of the vital force,) owing to the absence of food, is entirely suppressed. In several, apparent death occurs in consequence of the low temperature and of the diminution of vital energy thus produced; in others, the involuntary motions continue, and the animal preserves a temperature independent of the surrounding temperature. The respirations go on; oxygen, the condition which determines the production of heat and force, is absorbed now as well as in the former state of the animal; and previous to the winter sleep, we find all those parts of their body, which in themselves are unable to furnish resistance to the action of the oxygen, and which, like the intestines and membranes, are not destined for the change of matter, covered with fat; that is, surrounded by a substance which supplies the want of resistance. If we now suppose, that the oxygen absorbed during the winter sleep combines, not with the elements of living tissues, but with those of the fat, then the living part, although a certain momentum of motion be expended in keeping up the circulation, will not be separated and expelled from the body. With the return of the higher temperature, the capacity of growth increases in the same ratio, and the motion of the blood increases with the absorption of oxygen. Many of these animals become emaciated during the winter sleep, others not till after awaking from it. In hybernating animals the active force of the living parts is exclusively devoted, during hybernation, to the support of the involuntary motions. The expenditure of force in voluntary motion is entirely suppressed. In contradistinction to these phenomena, we know that, in the case of excess of motion and exertion, the active force in living parts may be exclusively and entirely consumed in producing voluntary mechanical effects; in such wise that no force shall remain available for the involuntary motions. A stag may be hunted to death; but this cannot occur without the metamorphosis of all the living parts of its muscular system, and its flesh becomes uneatable. The condition of metamorphosis into which it has been brought by an enormous consumption both of force and of oxygen continues when all phenomena of motion have ceased. In the living tissues, all the resistance offered by the vital force to external agencies of change is entirely destroyed. But however closely the conditions of the ANIMAL CHEMISTRY. 72 production of heat and of force may seem to be connected together, with reference to mechanical effects, yet the disengagement of heat can in no way be considered as in itself the only cause of these effects. All experience proves, that there is, in the organism, only one source of mechanical power; and this source is the conversion of living parts into lifeless, amorphous compounds. Proceeding from this truth, which is independent of all theory, animaL life may be viewed as determined by the mutual action of opposed forces; of which one class must be considered as causes of increase, (of supply of matter,) and the other as causes of diminution (of waste of matter.) The increase of mass is effected in living parts by the vital force; the manifestation of this power is dependent on heat; that is, on a certain temperature peculiar to each specific organism. The cause of waste of matter is the chemical action of oxygen ; and its manifestation is dependent on the abstraction of heat as well as on the expenditure of the vital force for mechanical purposes. The act of waste of matter is called the change of matter; it occurs in consequence of the absorption of oxygen into the substance of living parts. This absorption of oxygen occurs only when the resistance which the vital force of the living parts opposes to. the chemical action of the oxygen is weaker than that chemical action; and this weaker resistance is determined by the abstraction of heat, or by the expenditure in mechanical motions of the available force of living parts. By the combination of the oxygen introduced into the arterial blood with such constituents of the body as offer no resistance to its action, the temperature necessary for the manifestation of vital activity is produced. From the relations between the consumption of oxygen on the one hand and the change of matter and developement of heat on the other, the following general rules maybe deduced. For every proportion of oxygen which enters into combination in the body, a corresponding proportion of heat must be generated. The sum of force available for mechanical purposes must be equal to the sum of vital forces of all tissues adapted to the change of matter. If, in equal times, unequal quantities of oxygen are consumed, the result is obvious, in an unequal amount of heat liberated, and of mechanical force. When unequal amounts of mechanical force are expended, this determines the absorption of corresponding and unequal quantities of oxygen. For the conversion of living tissues into lifeless compounds, and for the combination of oxygen with such constituents of the body as have an affinity for it, time is required. In a given time, only a limited amount of mechanical force can be manifested, and only a limited, amount of heat can be liberated. That which is expended, in mechanical effects, in the shape of velocity, is lost in time; that is to say, the more rapid the motions are, the sooner or the more quickly is the force exhausted. The sum of the mechanical force produced in a given time is equal to the sum of force necessary, during the same time, to produce the voluntary and involuntary motions; that is, all the force which the heart, intestines, &c, require for their motions is lost to the voluntary motions. The amount of azotized food necessary to restore the equilibrium between waste and supply is directly proportional to the amount of tissues metamorphosed. The amount of living matter, which in the body loses the condition of life, is, in equal temperatures, directly proportional to the mechanical effects produced in a given time. The amount of tissue metamorphosed in a given time may be measured by the quantity of nitrogen in the urine. The sum of the mechanical effects produced in two individuals, in the same temperature, is proportional to the amount of nitrogen in their urine; whether the mechanical force has been employed in voluntary or involuntary motions, whether it has been consumed by the limbs or by the heart and other viscera. That condition of the body'which is called health includes the conception of an equilibrium among all the causes of waste and of supply; and thus animal life is recognized as the mutual action of both; and appears as an alternating destruction and restoration of the state of equilibrium. In regard to its absolute amount, the waste and supply of matter is, in the different periods of life, unequal; but, in the state of health, the available vital force must always be considered as a constant quantity, corresponding to the sum of living particles. Growth, or the increase of mass, stands, at every age, in a, fixed relation to the amount of vital force consumed as moving power. The vital force, which is expended for mechanical purposes, is subtracted from the sum of the force available for the purpose of increase of mass. The active force, which is consumed in the body in overcoming resistance (in causing increase of mass) cannot, at the same time, be employed to produce mechanical effects. Hence it follows necessarily, that when, as in childhood, the supply exceeds the waste of matter, the mechanical effects produced must be less in the same proportion. With the increase of mechanical effects MOTION IN THE ANIMAL ORGANISM. 73 produced, the capacity of increase of mass or of the supply of waste in living tissues must diminish in the same proportion. A perfect balance between the consumption of vital force for supply of matter and that for mechanical effects occurs, therefore, only in the adult slate. It is at once recognized in the complete supply of the matter consumed. In old age more is wasted; in childhood more is supplied than wasted. The force available for mechanical purposes in an aduJf man is reckoned, in mechanics, equal to the £th of his own weight, which he can move during eight hours, with a velocity of five feet in two seconds. If the weight of a man be 150 lbs., his force is equal to a weight of 30 lbs. carried by him to a distance of 72,000 feet. For every second his momentum of force is = 30 x2-5=75 lbs.; and for the whole day's work his momentum of motion is = 30 X 72,000 = 216,000. By the restoration of the original weight of his body, the man collects again a sum of force which allows him, next day, to produce, without exhaustion, the same amount of mechanical effects. This supply offorce is furnished in a seven hours' sleep. In manufactories of rolled iron it frequently happens, that the pressure of the engine, going at its ordinary rate, is not sufficient to force a rod of iron of a certain thickness to pass below the cylinders. The workman, in this case, allows the whole force of the steam to act on the revolving wheel, and not until this has acquired a great velocity does he bring the rod under the rollers; when it is instantly flattened with great ease into a plate, while the wheel gradually loses the velocity it had acquired. What the wheel gained in velocity the roller gained in force; by this process force was obviously collected, accumulated in the velocity ; but in this sense force does not accumulate in the living organism. The restoration of force is effected, in the animal body, by the transformation of the separated parts, destined for the production of force, and by the expenditure of the active vital force in causing/ormaiion of new parts ; and, with the restoration of the separated or effete parts, the organism recovers a force equal to that which has been expended. It is plain, that the vital force manifested, during sleep, in the formation of new parts, must be equal to the whole sum of the moving power expended in the waking state in all mechanical effects whatever, plus a certain amount of force, which is required for carrying on those involuntary motions which continue during sleep. From day today, the labouring man, with sufficient food, recovers, in seven hours' sleep, the whole sum of force; and without reckoning the force necessary for the involuntary motions which may be considered equal in all men, we may assume, that the mechanical force available for work is di- 10 rectly proportional to the number of hours of sleep. The adult man sleeps 7 hours, and wakes 17 hours; consequently, if the equilibrium he restored in 24 hours, the mechanical effects produced in 17 hours must be equal to the effects produced during 7 hours in the shape of formation of new parts. An old man sleeps only 3£ hours; and if every thing else be supposed the same as in the case of the adult, he will be able, at all events, to produce half of the mechanical effects produced by an adult of equal weight; is, he will be able to carry only 15 lbs. instead of 30 to the same distance. The infant at the breast sleeps 20 hours and wakes only four; the active force consumed in formation of new parts is, in this case, to that consumed in mechanical effects (in motion of the limbs) as 20 to 4; but his limbs possess no momentum of force, for he cannot yet support his own body. If we assume, that the aged man and infant consume in mechanical effects a quantity of force corresponding to the proportion available in the adult, then the mechanical effects are proportional to the number of waking hours, the formation of new parts to the number of hours of sleep, and we shall have: Force expended in Force expended in mechanical effects, formation of new parts. In the adult . . 17 : 7 In the infant. . 4 : 20 In the old man .20 : 4 In the adult a perfect equilibrium takes place between waste and supply; in the old man and in the infant, waste and supply are not in equilibrium. If we make the consumption of force in the 17 waking hours equal to that required for the restoration of the equilibrium during sleep = 100 =17 waking hours, = 7 hours of sleep, we obtain the following proportions. The mechanical effects are to those in the shape of formation of new parts: In the adult man = 100: 100 In the infant . . = 25 : 250 In the old man . = 125 : 50 Or the increase of mass to the diminution by waste': In the adult man = 100 : 100 In the infant . . = 100 : 10 In the old man . = 100 : 250 It is consequently clear, that if the old man performs an amount of work proportional to the sleeping hours of the adult, the waste will he greater than the supply ; that is, his body will rapidly decrease in weight, if he carry 15 lbs. to the distance of 72,000 feet with a velocity of 2£ feet in the second ; but he will be able, without injury, to carry 6 lbs. to the same distance. In the infant the increase is to the decrease as 10 to 1, and consequently, if we in his case increase the expenditure of force in mechanical effects to ten times its proper amount, there will thus be established only an equilibrium between waste and supply. G 74 ANIMAL CHEMISTRY. The child, indeed, will not grow, but neither will it lose weight. If, in the *adult man, the consumption of force for mechanical purposes in 24 hours be augmented beyond the amount restorable in seven hours of sleep, then, if the equilibrium is to be restored, less force, in the same proportion, must be expended in mechanical effects in the next 24 hours. If this be not done, the mass of the body decreases, and the state characteristic of old age more or less decidedly supervenes. With every hour of sleep the sum of available force increases in the old man, or proaches the state of equilibrium between waste and supply which exists in the adult. It is further evident, that if a part of the force which is available for mechanical purposes, without disturbing the equilibrium, should not be consumed in moving the limbs, in raising weights, or in other labour, it will be available for involuntary motions. If the motion of the heart, of the fluids, and of the intestines (the circulation of the blood and digestion) are accelerated in proportion to the amount of force not consumed in voluntary motions, the weight of the body will neither increase or diminish in 24 hours. The body, therefore, can only increase in mass, if the force accumulated during sleep, and available for mechanical purposes, is employed neither for voluntary nor for involuntary motions. The numerical values above given for the expenditure of force in the human body refer,, as has been expressly stated, only to a given, uniform temperature. In a different temperature, and with deficient nourishment, all these proportions must be changed. If we surround a part of the body with ice or snow, while other parts are left in the natural state, there occurs, more or less quickly, in consequence of the loss of heat, an acceleiated change of matter in the cooled part. . The resistance of the living tissues to the action of oxygen is weaker at the cooled part than in the other parts; and this, in its effects, is equivalent to an increase of resistance in these other parts. The momentum of force of the vitality in the parts which are not cooled is expended, as before, in mechanical motion; but the whole action of the inspired oxygen is exerted on the cooled part. If we imagine an iron cylinder, into which we admit steam under a certain pressure, then if the force with which the f>articles of the iron cohere be equal to the brce which tends to separate them, an equilibrium will result; that is, the whole effect of the steam will be neutralized by the resistance. But if one of the sides of the cylinder be moveable, a piston-rod, for example, and offer to the pressure of the steam a less resistance than other parts, the whole force will be expended in moving this one side—that is, in raising the piston-rod. • If we do not introduce fresh steam (fresh force) an equilibrium will soon be established. The piston-rod resists a certain force without moving, but is raised by an increased pressure. When this excess of force has been consumed in motion, it cannot be raised higher; but if new vapour be continually admitted, the rod will continue to move. In the cooled part of the body, the living tissues offer a less resistance to the chemical action of the inspired oxygen; the power of the oxygen to unite with the elements of the tissues is, at this part, -exalted. When the part has once lost its condition of life, resistance entirely ceases; and in consequence of the combination of the oxygen with the elements of the metamorphosed tissues, a greater amount of heat is liberated. For a given amount of oxygen, the heat produced is, in all cases, exactly the same. In the cooled part, the change of matter, and with it the disengagement of heat, increases ; while in the other parts the change of matter and liberation of heat decrease. But when the cooled part, by the union of oxygen with the elements of the metamorphosed tissues, has recovered its original temperature, the resistance of its living particles to the oxygen conveyed to them again increases, and, as the resistance of other parts is now diminished, a more rapid change of matter now occurs in them, their temperature rises, and along with this, if the cause of the change of matter continues to operate, a larger amount of vital force becomes available for mechanical purposes. Let us now suppose that heat is abstracted from the whole surface of the body; in this case the whole action of the oxygen will be directed to the skin, and in a short time the change of matter must increase throughout the body. Fat, and all such matters as are capable of combining with the oxygen which is brought to them in larger quantity than usual, will be expelled from the body in the form of oxidized compounds. III.—Theory of Disease. Every substance or matter, every chemical or mechanical agency, which changes or disturbs the restoration of the equilibrium between the manifestations of the causes of waste and supply, in such a way as to add its action to the causes of waste, is called a cause of disease. Disease occurs when the sum of vital force, which tends to neutralize all causes of disturbance, (in other words, when the resistance offered by the vital force,) is weaker than the acting cause of disturbance. Death is that condition in which all resistance on the part of the vital force entirely ceases. So long as this condition is not established, the living tissues continue to offer resistance. To the observer, the action of a cause of disease exhibits itself in the disturbance of the proportion between waste and supply which is proper to each period of life. In medicine, every abnormal condition of supply or of waste, in all parts or in a single part of the body, is called disease. THEORY OF DISEASE. 75 It is evident that one and the same cause of disease will produce in the organism very different effects, according to the period of life; and that a certain amount of disturbance, which produces disease in the adult state, may be without influence in childhood or in old age. A cause of disease may, when it is added to the cause of waste in old age, produce death (annihilate all resistance on the part of the vital force;) while in the adult state it may produce only a disproportion between supply and waste; and in infancy, only an equilibrium between supply and waste (the abstract state of health.) A cause of disease which strengthens the causes of supply, either directly or indirectly by weakening the action of the causes of waste, destroys, in the child and in the adult, the relative normal state of health; while in old age it merely brings the waste and supply into equilibrium. A child, lightly clothed, can bear cooling by a low external temperature without injury to health; the force available for mechanical purposes and the temperature of its body increases with the change of matter which follows the cooling; while a higher temperature, which impedes the change of matter, is followed by disease. On the other hand, we see, in hospitals and charitable institutions (in Brussels, for example) in which old people spend the last years of life, when the temperature of the dormitory in winter sinks 2 or 3 degrees below the usual point, that by this slight degree of cooling the death of the oldest and weakest males as well as females is brought about. They are found lying tranquilly in bed, without the slightest symptoms of disease, or of the usual recognizable causes of death. A deficiency of resistance, in a living part, to the cause of waste is, obviously, a deficiency of resistance to the action of the oxygen of the atmosphere. When, from any cause whatever, this resistance diminishes in a living part, the change of matter increases in an equal degree. Now, since the phenomena of motion in the animal body are dependent on the change of matter, the increase of the change of matter in any part is followed by an increase of all motions. According to the conducting power of the nerves, the available force is carried away by the nerves of involuntary motion alone, or by all the nerves together. Consequently, if, in consequence of a diseased transformation of living tissues, a greater amount of force be generated than is required for the production of the normal motions, it is seen in an acceleration of all or some of the involuntary motions, as well as in a higher temperature of the diseased part. This condition is called fever. When a great excess of force is produced by change of matter, the force, since it can only be consumed by motion, extends itself to the apparatus of voluntary motion. This state is called a febrile paroxysm. In consequence of the acceleration of the circulation in the state of fever, a greater amount of arterial blood, and, consequently of oxygen, is conveyed to the diseased part, as well as to all other parts; and if the active force in the healthy parts continue uniform, the whole action of the excess of oxygen must be exerted on the diseased part alone. According as a single organ, or a system of organs, is affected, the change of matter extends to one part alone, or to the whole affected system. Should there be formed, in the diseased parts, in consequence of the change of matter, from the elements of the blood or of the tissue, new products, which the neighbouring parts cannot employ for their own vital functions; —should the surrounding parts, moreover, be unable to convey these products to other parts, where they may undergo transformation, then these new products will suffer, at the place where they have been formed, a process of decomposition analogous to fermentation or putrefaction. In certain cases, medicine removes these diseased conditions, by exciting in the vicinity of the diseased part, or •in any convenient situation, an artificial diseased state (as by blisters, sinapisms, or setons); thus diminishing, by means of artificial disturbance, the resistance offered to the external causes of change in these parts by the vital force. The physician succeeds in putting an end to the original diseased condition, when the disturbance artificially excited (or the diminution of resistance in another part) exceeds in amount the diseased state to be overcome. The accelerated change of matter and the elevated temperature in the diseased part show, that the resistance offered by the vital force to the action of oxygen is feebler than in the healthy state. But this resistance only ceases entirely when death takes place. By the artificial diminution of resistance in another part, the resistance in the diseased organ is not indeed directly strengthened; but the chemical action (the cause of the change of matter) is diminished in the diseased part, being directed to another part, where the physician has succeeded in producing a still more feeble resistance to the change of matter (to the action of oxygen). A complete cure of the original disease occurs, when external action and resistance, in the diseased part, are brought into equilibrium. Health and the restoration of the diseased tissue to its original condition follow, when we are able so far to weaken the disturbing action of oxygen, by any means, that it becomes inferior to the resistance offered by the vital force, which, although enfeebled, has never ceased to act; for this proportion between these causes of change is the uniform and necessary condition of increase of mass in the living organism. 76 ANIMAL CHEMISTRY. In cases of a different kind, where artificial external disturbance produces no effect, the physician adopts other indirect methods to exalt the resistance offered by the vital force. These methods, the result of ages of experience, are such, that the most perfect theory could hardly have pointed them out more acutely or more justly than has been done by the observation of sagacious f>ractitioners. He diminishes, by bloodetting, the number of the carriers of oxygen, (the globules,) and by this means the conditions of change of matter; he excludes from the food all such matters as are capable of conversion into blood; he gives chiefly or entirely non-azotized food, which supports the respiratory process, as well as fruit and vegetables, which contain the alkalies necessary for the secretions. If he succeed, by these means, in diminishing the action of the oxygen in the blood on the diseased part, so far that the vital force of the latter, its resistance, in the smallest degree overcomes the chemical action ; and if he accomplish this, without arresting the functions of the other organs, then restoration to health is certain. To the method of cure adopted in such cases, if employed with sagacity and acute observation^there is added, as we may call it, an ally on the side of the diseased organ, and this is the vital force of the healthy parts. For, when blood is abstracted, the external causes of change are diminished also in them, and their vital force, formerly neutralized by these causes, now obtains the preponderance. The change of matter, indeed, is diminished throughout the body, and with it the phenomena of motion : but the sum of all resisting powers, taken together, increases in proportion as the amount of the oxygen acting on them in the blood is diminished. In the sensation of hunger, this resistance, in a certain sense, makes itself known; and the preponderating vital force exhibits itself, in many patients, when hunger is felt, in the form of an abnormal growth, or in abnormal metamorphosis of certain parts of organs. Sympathy is the transference of diminished resistance from one part, not exactly to the next, but to more distant organs, when the functions of both mutually influence each other. When the action of the diseased organ is connected with that of another—when, for example, the one no longer produces the matters necessary to the performance of the functions of the other—then the diseased condition is transferred, but only apparently, to the latter. In regard to the nature and essence of the vital force, we can hardly deceive ourselves, when we reflect, that it behaves, in all its manifestations, exactly like other natural forces ; that it is devoid of consciousness or of volition, and is subject to the action of a blister. The nerves, which accomplish the voluntary and involuntary motions in the body, ' are, according to the preceding exposition, : not the producers, but only the conductors 1 of the vital force; they propagate motion, and behave towards other causes of motion, which in their manifestations are analogous to the vital force, towards a current of electricity, for example, in a precisely analogous manner. They permit the current to traverse them, and present, as conductors of electricity, all the phenomena which they exhibit as conductors of the vital force. In the present state of our knowledge, no one, probably, will imagine that electricity is to be considered as the cause of the phenomena of motion in the body; but still, the medicinal action of electricity, as well as that of a magnet, which, when placed in contact with the body, produces a current of electricity, cannot be denied. For to the existing force of motion or of disturbance there is added, in the electrical current, a new cause of motion and of change in form and structure, which cannot be considered as altogether inefficient. Practical medicine, in many diseases, makes use of cold in a highly rational manner, as a means of exalting and accelerating, in an unwonted degree, the change of matter. This occurs especially in certain morbid conditions in the substance of the centre of the apparatus of motion 5 when a glowing heat and a rapid current of blood towards the head point out an abnormal metamorphosis of the brain. When this condition continues beyond a certain time, experience teaches that all motions in the body cease. If the change of matter be chiefly confined to the brain, then the change of matter, the generation of force, diminishes in all other parts. By surrounding the head with ice, the temperature is lowered, but the cause of the liberation of heat continues; the metamorphosis, which decides the issue of the disease, is limited to a short period. We must not forget, that the ice melts and absorbs heat fiom the diseased part; that if the ice be removed before the completion of the metamorphosis, the temperature again rises; that far more heat is removed by means of ice than if we were to surround the head with a bad conductor of heat. There has obviously been liberated in an equal time a far larger amount of heat than in the state of health; and this is only rendered possible by an increased supply of oxygen, which* must have determined a more rapid change of matter. The self-regulating steam engines, in which, to produce a uniform motion, the human intellect has shown the most admirable acuteness and sagacity, furnish no unapt image of what occurs in the animal body. Every one knows, that in the tube which conveys the steam to the cylinder where the piston-rod is to be raised, a stop-cock of peculiar construction is placed, through which all the steam must pass. By an arrangement connected with the- regulating THEORY OP RESPIRATION. 77 G wheel, thWftop-cock opens when the wheel moves slower, and closes more or less completely when the wheel moves faster than is required for a uniform motion." When it opens, more steam is admitted, (more force,) and the motion of the machine is accelerated. When it shuts, the steam is more or less cut off, the force acting on the pistonrod diminishes, the tension of the steam increases, and this tension is accumulated for subsequent use. The tension of the vapour, or the force, so to speak, is produced by change of matter, by the combustion of coals in the fire-place. The force increases (the amount of steam generated and its tension increase) with the temperature in the fire-place, which depends on the supply of coals and of air. There are in these engines other arrangements, all intended for regulation. When the tension of steam in the boiler rises beyond a certain point, the passages for admission of air close themselves; the combustion is retarded, the supply of force (of steam) is diminished. When the engine goes slower, more steam is admitted to the cylinder, its tension diminishes, the air passages are opened, and the cause of disengagement of heat (or production of,, force) increases. Another arrangement plies the fire-place incessantly with coals In proportion as they are Wanted. If we now lower the temperature at any part of the boiler, the tension within is diminished; this is immediately seen in the regulators of force, which act precisely as if we had removed from the boiler a certain •quantity of steam (force.) The regulator and the air-passages open, and the machine supplies itself with more coals. The body, in regard to the production of heat and of force, acts just like one of these machines. With the lowering of the external temperature, the respirations become deeper and more frequent; oxygen is supplied in greater quantity and of greater density ; the change of matter is increased, and more food must be supplied, if the temperature of the body is to remain unchanged. It is hardly necessary to mention, that in the body the tension of vapour cannot, any more than an electrical current, be considered the cause of the production of force. From the theory of disease developed in the precqfling pages, it follows obviously, i that a deceased condition once established, < in any part of the body, cannot be made to : disappear by the chemical action of a remedy. A limit may be put by a remedy i to an abnormal process of transformation; i that process may be accelerated or retarded; but this alone does not restore the normal i (healthy) condition. < The art of the physician consists in the knowledge of the means which enable him to exercise an influence on the duration of the disease; and in the removal of all disturbing causes, the action of which strengthens or increases that of the actual cause of disease. It is only by a just application of its principles that any theory can produce really beneficial results. The very same method of cure may restore health in one individual, which, if applied to another, may prove fatal in its effects. Thus in certain inflammatory diseases, and in highly muscular subjects, the antiphlogistic treatment has a very high value; while in other cases blood-letting produces unfavourable results. The vivify-, ing agency of the blood must ever continue to be the most importani condition in the restoration of a disturbed equilibrium, which result is always dependent on the saving of time; and the blood must, therefore, be considered and constantly kept in view, as the ultimate and most powerful cause of a lasting vital resistance, as well in the diseased as in the unaffected parts of the body. It is obvious, moreover, that in all diseases where the formation of contagious matter and of exanthemata is accompanied by fever, two diseased conditions simultaneously exist, and two processes are simultaneously completed ; and that the blood, as it were by re-action (i. e. fever) becomes a means of cure, as being the carrier of that (oxygen) without the aid of which pne diseased products cannot be rendered harmless, destroyed, or expelled from the body; a means of cure by which, in short, neutralization or equilibrium is effected. IV. Theory op Respiration.—During the passage of the venous blood through the lungs, the globules change their colour; and with this change of colour, oxygen is absorbed from the atmosphere. Further, for every volume of oxygen absorbed, an equal volume of carbonic acid is, in most cases, given out. The red globules contain a compound of iron; and no other constituent of the body contains iron. Whatever change the other constituents of the blood undergo in the lungs, thus much is certain, that the globules of venous blood experience a change of colour, and that this change depends on the action of oxygen. Now we observe that the globules of arterial blood retain their colour in the larger vessels, and lose it only during their passage through the capillaries. All those constituents of venous blood, which are capable of combining with oxygen, take up a corresponding quantity of it in the lungs. Experiments made with arterial serum have shown, that when in contact with oxygen it does not diminish the volume of that gas. Venous blood, in contact with oxygen, is reddened, while oxygen is absorbed; and a corresponding quantity of carbonic acid is formed. It is evident that the change of colour in the venous globules depends on the combination of some one of their elements with oxygen; and that this absorption of oxygen is attended with the separation of a, certain quantity of carbonic acid gas. \ ANIMAL CHEMISTRY. 78 This carbonic acid is not separated from the serum; for the serum does not possess the property, when in contact with oxygen, of giving off carbonic acid. On the contrary, when separated from the globules, it absorbs from half its volume to an equal volume of carbonic acid, and, at ordinary temperatures, is not saturated with that gas. (See the article " Blut," in the " Handworterbuch der Chemie, von Poggendorff, Wohler, und Liebig, p. 877.) Arterial blood, when drawn from the body, is soon altered; its florid colour becomes, dark red. The florid blood, which owes its colour to the globules, becomes dark by the action of carbonic acid, and this change of colour affects the globules, for florid blood absorbs a number of gases which do not dissolve in the fluid part of the blood when separated from the globules. It is evident, tlierefore, tluit the globules lutve the power of combining with gases. The globules of the blood change their colour in different gases; and this change may be owing either to a combination or to a decomposition. Sulphuretted hydrogen turns them blackish green and finally black; and the originaL red colour cannot, in this case, be restorer by contact with oxygen. Here a decomposition has obviously taken place. The globules darkened by carbonic acid become again florid in oxygen, with disengagement of carbonic acid. The same thing takes place in nitrous oxide. It is clear that they have here undergone no decomposition, and, consequently, they possess the power of combining with gases, while the compound tluty form with carbonic acid is destroyed by oxygen. When left to themselves, out of the body, the compound formed with oxygen again becomes dark, but does not recover its florid colour a second time by the action of oxygen. The globules of the blood contain a compound of iron. From the never-failing presence of iron in red blood, we must conclude, that it is unquestionably necessary to animal life; and, since physiology has proved, that the globules take no share in the process of nutrition, it cannot be doubted that they play a part in the process of respiration. The compound of iron in the globules has the characters of an oxidized com- Eound; for it is decomposed by sulphuretted ydrogen, exactly in the same way as the oxides or other analogous compounds of iron. By means of diluted mineral acids, peroxide (sesquioxide) of iron may be extracted, at the ordinary temperature, from the fresh or dried red colouring matter of the blood. The characters of the compounds of iron may, perhaps, assist us to explain the share which that metal takes in the respiratory process. No other metal can be compared with iron, for the remarkable properties of its compounds. The compounds of possess the property of depriving other oxidized compounds of oxygen; while the compounds of peroxide of iron, under other circumstances, give up oxygen with the utmost facility. Hydrated peroxide of iron, in contact with organic matters destitute of sulphur, is converted into carbonate of the protoxide. Carbonate of protoxide of iron, in contact with water and oxygen, is decomposed; all the carbonic acid is given off, and, by absorption of oxygen, it passes into the hydrated peroxide, which may again be converted into a compound of the protoxide. Not only the oxides of iron, but also the cyanides of that metal, exhibit similar properties. Prussian blue contains iron in combination with all the organic elements of the bodv; hydrogen and oxygen (water) carbon and nitrogen (cyanogen.) When it is exposed to light, cyanogen is given off, and it becomes white; in the dark it extracts oxygen, and recovers its blue colour. All these observations, taken together, lead to the opinion that the globules of artejial blood contain a compound of iron saturated with oxygen, which, in the. living blood, loses its oxygen during its passage through the capillaries. The same thing occurs when it is separated from the body, and begins to undergo decomposition (to putrefy.) The compound, rich in oxygen, passes, therefore, by the loss of oxygen (reduction) into one far less charged with that element. One of the products of oxidation, formed in this process is carbonic acid. The compound of iron in the venous blood possesses the property of combining with carbonic acid; and it is obvious, that the globules of the arterial blood, after losing a part of their oxygen, will, if they meet with carbonic acid, combine with that substance. When they reach the lungs, they wil' again take up the oxygen they have lost; for every volume of oxygen absorbed, a corresponding volume of carbonic acid will be separated; they will return lo their former state; that is, they will again acquire the power of giving off oxygen. For every volume of oxygen which the globules can give off, there will be formed (as carbonic acid contains its own volume of oxygen, without condensate) neither more nor less than an equal volume of carbonic acid. For every volume of oxygen which the globules are capable of absorbing, no mote carbonic acid can possibly be separated than the volume of oxygen can produce. When carbonate of protoxide of iron, by the absorption of oxygen, passes into the hydrated peroxide, there are given off, for every volume of oxygen necessary to the change from protoxide to peroxide, four volumes of carbonic acid gas. But from one volume of oxygen only one volume of cabronic acid can be produced; THEORY OF RESPIRATION. 79 and the absorption of one volume of oxygen can only cause, directly, the separation of an equal body of carbonic acid. Consequently, the substance or compound which has lost its oxygen, during the passage of arterial into venous blood, must have been capable of absorbing or combining with carbonic acid; and We find, in point of fact, that the living blood is never, in any state, saturated with carbonic acid; that it is capable of taking up an additional quantity, without any apparent disturbance of the function of the globules. Thus, for example, after drinking effervescing wines, beer, or mineral waters, more carbonic acid must necessarily be expired than at other times. In all cases, where the oxygen of the arterial globules has been partly expended, otherwise than in the formation of carbonic acid, the amount of this latter gas expired will correspond exactly with that which has been formed; less, however, will be given out after the use of fat and of still wines, than after champagne. According to the views now developed, the globules of arterial blood, in their passage through the capillaries, yield oxygen to certain constituents of the body. A small portion of this oxygen serves to produce the change of matter, and determines the separation of living parts and their conversion into lifeless compounds, as well as the formation of the secretions and excretions. The greater part, however, of the oxygen is employed in converting into oxidized compounds the newly formed substances, which no longer form part of the living tissues. In their return towards the heart, the globules which have lost their oxygen combine with carbonic acid, producing venous blood; and, when they reach the lungs, an exchange takes place between this carbonic acid and the oxygen of the atmosphere. The organic compound of iron, which exists in venous blood, recovers in the lungs the oxygen it has lost, and, in consequence of this absorption of oxygen, the carbonic acid in combination with it is separated. All the compounds present in venous blood, which have any attraction for oxygen, are converted, in the lungs, like the globules, into more highly oxidized compounds ; a certain amount of carbonic acid is formed, of which a part always remains dissolved in the serum of the blood. The quantity of carbonic acid dissolved, or, of that combined with soda, must be equal in venous and arterial blood, since both have the same temperature; but arterial blood, when drawn, must, after a short time, contain a larger quantity of carbonic acid than venous blood, because the oxygen of the globules is expended in producing that compound. Hence, in the animal organism, two processes of oxidation are going on; one in the lungs, the other in the capillaries. By means of the former, in spite of the degree of cooling, and of the increased evapora- tion which takes place there, the constant temperature of the lungs is kept up; while the heat of the rest of the body is supplied by the latter. A man, who expires daily 13*9 oz. of carbon, in the form of carbonic acid, consumes, in 24 hours, 37 oz. of oxygen, which occupy a space equal to 807 litres=51,648 cubic inches (Hessian.) If we reckon 18 respirations to a minute, we have, in 24 hours, 25,920 respirations ; and, consequently, in each respiration, there are taken into the blood fi§f§=l'99 cubic inch of oxygen. In one minute, therefore, there are added to the constituents of the blood 18 X 1*99= 35-8 cubic inches of oxygen, which, at the ordinary temperature, weigh rather less than 12 grains. If we now assume, that in one minute 10 lbs. of blood pass through the lungs, (Miiller, Physiologie, vol. i. p. 345,) and that this quantity of blood measures 320 cubic inches, then 1 cubic inch of oxygen unites with 9 cubic inches of blood, very nearly. According to the researches of Denis, Richardson, and Nasse (Handworterbuch der Physiologie, vol. i. p. 138,) 10,000 parts of blood contain 8 parts of peroxide of iron. Consequently, 76,800 grains (10 lbs. Hessian) of blood contain 61*54 grains of peroxide of iron in arterial blood, — 55-14 of protoxide in venous blood. Let us now assume that the iron of the globules of venous blood is in the state of protoxide. It follows, that 55-14 grains of protoxide of iron, in passing through the lungs, take up, in one minute, 6-40 grains of oxygen (the quantity necessary to convert it into peroxide.) But since, in the same time, the 10 lbs. of blood have taken up 12 grains of oxygen, there remain 5-60 grains of oxygen, which combine with the other constituents of the blood. Now, 55-14 grains of protoxide of iron combine with 34*8 grains of carbonic acid, which occupy the volume of 73 cubic inches. It is obvious, therefore, that the amount of iron present in the blood, if in the state of protoxide, is sufficient to furnish the means of carrying or transporting twice as much carbonic acid as can possibly be formed by the oxygen absorbed in the lungs. The" hypothesis just developed rests on well-known observations, and, indeed, explains completely the process of respiration, as far as it depends on the globules of the blood. It does not exclude the opinion that carbonic acid may reach the lungs in other ways; that certain other constituents of the blood may give rise to the formation of carbonic acid in the lungs. But all this has no connexion with that vital process by which the heat necessary for the support of life is generated in every part of the body. Now it is this alone which, for the present, can be considered as the object truly worthy of investigation. It is not, indeed, uninteresting to inquire, why dark blood becomes 80 ANIMAL CHEMISTRY. florid by the action of nitre, common salt, &c; but this question has no relation to the natural respiratory process. The frightful effects of sulphuretted hydrogen, and of prussic acid, which, when inspired, put a stop to all the phenomena of motion in a few seconds, are explained in a natural manner by the well-known action of these compounds on those of iron, when alkalies are present; and free alkali is never absent in the blood. Let us suppose that the globules lose their property of absorbing oxygen, and of afterwards giving up this oxygen and carrying off the resulting carbonic acid; such a hypothetical state of disease must instantly become perceptible in the temperature and other vital phenomena of the body. The change of matter will be arrested, while yet the vital motions will not be instantly stopped. The conductors of force, the nerves, will convey, as before, to the heart and intestines the power necessary for their functions. This power they will receive from the muscular system, while, as no change of matter takes place in the latter, the supply must soon fail. As no change of matter occurs, 1 no lifeless compounds are separated, neither bile nor urine can be formed; and the temperature of the body must sink. This state of matters soon puts a stop to the process of nutrition, and sooner or later death must follow, but unaccompanied by febrile symptoms, which in this case is a very important fact. This example has been selected in order to show the importance and probable advantage of an examination of the blood in analogous diseased conditions. It cannot be, in the slightest degree, doubtful that the function ascribed to the blood globules may be considered as fully explained and cleared up, if, in such morbid conditions, we shall discover a change in their form, structure, or chemical characters, a change which must be recognizable by the use of appropriate re-agents. If we consider the force which determines the vital phenomena as a property of certain substances, this view leads of itself to a new and more rigorous consideration of certain singular phenomena, which these very substances exhibit, in circumstances in which they no longer make a part of living organisms. APPENDIX: CONTAINING THE ANALYTICAL EVIDENCE REFERRED TO IN THE SECTIONS IN WHICH ARE DESCRIBED THE CHEMICAL PROCESSES OF RESPIRATION, OF NUTRITION, AND OF THE METAMORPHOSIS OF TISSUES. %* The Notes correspond with the'numbers in parentheses in the text. All the Analyses quoted, which have the mark * attached, have been made in the chemical laboratory of the University of Giessen. INTRODUCTION' TO THE ANALYSES. The method formerly employed to exhibit the differences in composition of different substances, that, namely, of giving the proportions of the various elements in 100 parts, has been long abandoned by chemists; because it affords no insight into the relations which exist between two or more compounds. In order to give some proofs of this statement, we shall here state, in that form, the composition of aldehyde and acetic acid, of oil of bitter almonds and benzoic acid. Acetic acid. Aldehyde. Benzoic acid. Oil of bitter almonds. Carbon 40-00 55 024 69-25 79-56 Hydrogen 667 8-983 4-86 5-56 Oxygen 5333 35993 25.89 1488 Now aldehyde is converted into acetic acid, and oil of bitter almonds into benzoic acid, simply by the addition of oxygen, without any change in regard to the other elements. This important relation cannot be traced in the mere numerical results of analysis as above given; but if the composition of the related compounds be expressed in formulae, according to equivalents, the connexion in each case becomes obvious, even to him who knows no more of chemistry than that C represents an equivalent or combining portion of carbon, H an equivalent of hydrogen, and O an equivalent of oxygen. Formula i ¦— K of acetic acid. of aldehyde. C 4 H 4 0 4 . C 4 H 4 0 2 . Formula , A of benzoic acid. of oil of bitter almonds. C 14 H 6 0 4 . C ,4 H 6 0 2 . APPENDIX.—ANALYTICAL EVIDENCE. 81 These formulae are exact expressions of the results of analysis, which, in each of the two cases quoted, refer to a fixed quantity of carbon; in one to 4 equivalents, in the other to 14. They show, that acetic acid differs from aldehyde, and benzoic acid from oit of bitter almonds, only in the proportion of oxygen. Nor is it more difficult to understand the signification of the following formula. Cyamelide. 1 eq. cyanuric acid. 3 eq. hydrated cyanic acid. C 6 N 3 H 3 0 6 =-Cy 3 (=C 6 N 3 )0 3 3-f-3HO-=3(CyO-r-HO)=-—C6N3H306 6 0 3 H 3 N 6 =C«N 3 H 3 0 6 . (In these formulae, N represents an equivalent of nitrogen, and Cy an equivalent of cyanogen. This latter substance being composed of 2 equivalents of carbon and 1 eq. of nitrogen, Cy = C 2 N.) The first formula (that of Cyamelide) is what is called an empirical formula, in which the relative proportions of the elements are, indeed, exacdy known, but where we have not even a theory, far less any actual knowledge, of the order in which they are arranged. The second formula is intended to express the opinion that 3 eq. of cyanogen (= 6 eq. of carbon + 3 eq. of nitrogen) having united to form a compound atom or molecule, have combined with 3 eq. of oxygen and 3 eq. of water, to form 1 eq. of hydrated cyanuric acid. The third expresses the order in which the elements are supposed to be arranged in hydrated cyanic acid, the whole multiplied by 3. Each equivalent of cyanic acid is formed of 1 eq. of cyanogen, 1 eq. of oxygen, and 1 eq. of water; and hence the same number of atoms of each element, which together formed 1 eq. of cyanuric acid, is here so divided as to yield 3 eq. of cyanic acid. We have here, therefore, the same absolute and relative amount of atoms of each element, arranged in three different ways; yet in each of these the proportions of the elements, calculated for 100 parts, must of course be the same. It is easy, therefore, to see the advantage we possess by the use of formulae ; that, namely, of exhibiting the relations existing between compounds of different composition; and that also of expressing the actual, probable, or possible differences between substances whose composition, in 100 parts, is the same, while their properties, as in the case above quoted, are perfectly distinct. " It does not come within our province here to explain the method or rule by which the composition of a substance, in 100 parts, (as it is always obtained in analysis,) is expressed in a formula; we shall only describe the rule for calculating, from a given formula, the composition in 100 parts. For this purpose it must be noted that C, in a chemical formula, signifies a weight of carbon expressed by the number 76*437 (according to the most recent determinations 75-8 or 75*0, a variation which has no effect whatever on the formulae here adduced, all of which are calculated on the number 76*437) ; that H signifies a weight of hydrogen =-> 12*478; N a weight of nitrogen =177*04; and lastly, O a weight of oxygen = 100. The formula of proteine," C^N 6 !! 38^ 4 , expresses, therefore, 48 times 76*437 — 3668*88 carbon, 6 times 177*040 = 1062*24 nitrogen, 36 times 12*478 = 449*26 hydrogen, 14 times 100*000= 1400*00 oxygen. The sum gives a weight of Therefore— In 6580-38 parts of proteine are contained In 6580-38 ditto In 6580-38 ditto In 6580-38 ditto 6580-38 proteine. In 100 parts. 3668-88 carbon 55-742 1062-24 nitrogen 16-143 449-26 hydrogen 6-827 1400 00 oxygen 21-288 100-000 The actual results of analysis, reduced to 100 parts, when compared with the above numbers, will show how far the assumed formula is corect; or, supposing the formula ascertained, they will show the degree of accuracy displayed by the experimenter. Thus the proportions in 100 parts, calculated from the formula, furnish an important check to the operator, and, conversely, the formula calculated from his results, when compared with other known formulae, supplies a test of his accuracy, or of the purity of the substance analyzed. 11 ANIMAL CHEMISTRY. 82 NOTE (1,) p. 14. CONSUMPTION OP OXYGEN BY AN ADULT. Jin adult man. , » i ¦ s Carbon contained. consumes of oxygen produces of carbonic in the in 24 hours. acid in 24 hours. carbonic acid. According to « * « . • —» cubic in. grains. cubic in. grains. grains. Lavoisier and Seguin 46,037 15,661 14,930 8,584 2,820 French. Menzies .... 51,480 17,625 English. Davy ..... 45,504 15,751 31,680 17,811 4,853 do. Allen and Pepys . . 39,600 13,464 39,600 18,612 5,148 do. NOTE (2,) p. 14. composition of dry blood (see Note 28.) In 100 parts. In 4-8 Ibi. Hessian = 36.864 grains. Carbon. . . 51-96 . . . 19154-5 Hydrogen. . 7-25 . . . 2672-7 Nitrogen . . 1507 . . . 5555-4 Oxygen . . 21-30 . . . 78520 Ashes . . 4-42 . . . 1629-4 10000 36864-0 Grains. Grains. 19154-5 carbon form, with 50539-5 oxygen, carbonic acid. 2672-7 hydrogen do. 21415-8 do. water. Sum = 71955-3 do. Deduct oxygen present ? 7852-0 in blood . . . $ = Remain 64103 3 grains of oxygen, required for the complete combustion of 4-8 lbs. of dry blood. It is assumed in this calculation, that 24 lbs. of blood yield 4*8 lbs. (20 per cent.) of dry residue. The remainder, 80 per cent., is water. NOTE (3,) p. 14. determination op the amount op carbon expired. 1. Analysis op Faces. 2-356 dry faeces left 0-320 ashes (13-58 per cent.) 0-352 dry faeces yielded 0-576 carbonic acid, and 0-218 water. Lentils. 0-566 lentils, dried at 212°, yielded 0 910 carbonic acid, and 0-366 water. Pease. 1-060 pease, dried at 212°, left 0-037 ashes. 0-416 do. do. yielded 0-642 carbonic acid, and 0 241 water. Potatoes. 0-443 dried potatoes yielded 0-704 carbonic acid, and 0-248 water. Black Bread (Schwarzbrod.) 0-302 dried black bread yielded 0-496 carbonic acid, and 0-175 water. 0-241 do. 0-393 do. 0-142 do. From the above, which are the direct results of experiment, the composition in 100 parts is calculated as in the following table. 2. Composition Of Faeces. Of Black Bread. Of PotatoeSi Of Flesh. Playfair.* Boeckmann.* Boussingault. BcBckmann.* Carbon 45-24 ' 45-09 45-41 44-1 43-944 (See note 28.) Hydrogen 688 6-54 6-45 5-8 6-222 Oxvgfnf 3473 45 ' 12 4489 45<1 44-919 Ashes 13-15 3-25 3-25 5-d 4-915 100-00 100-00 100-00 100 0 100 000 Water 300-00 400-00 APPENDIX.—ANALYTICAL EVIDENCE. 83 Of Pease. Of Lentils. Of Beans. Playfair.* Playfair.* Playfair.* Carbon .... 35-743 37-38 38-24 Hydrogen . . . 5-401 554 5-84 Oxygfn } • ' • 39366 37-98 38-10 Ashes .... 3-490 3 20 3-71 Water .... 16-000 15-90 14-11 100-000 100 00 100 00 Fresh Meat. Potatoes. Black Bread. Boeckmann.* Boussingault.* Boeckmann.* Water . . 75 74-8 72-2 73-2 33 31-418 Dry Matter . 25 25-2 27-8 26-8 67 68-592 100 1000 100-0 100-0 100 100000 3. Calculation, with the help of the preceding data, of the amount of carbon expired by an adult*man. The following results are deduced from observations made (see table) on the average daily consumption of food, by from 27 to 30 soldiers in barracks for a month, or by 855 men for one day. The»food, consisting of bread, potatoes, meat, lentils, pease, beans, &,c, was weighed, with the utmost exactness, every day during a month (including even pepper, salt, and butter;) and each article of food was separately subjected to ultimate analysis. The only exceptions, among the men, to the uniform allowance of food, were three soldiers of the guard, who, in addition to the daily allowance of 2 lbs. of bread, received, during each of the periods allotted for the pay of the troops, 2£ lbs. extra; and one drummer who, in the same period, left 2£ lbs. unconsumed. According to an approximative report by the sergeant-major, each soldier consumes daily, on an average, out of barracks, 3 oz. of sausage, £ oz. of butter, £ pint of beer, and A pint of brandy; the carbon of which articles amounts to more than double that of the faeces and urine taken together. In the soldier, the fasces amount daily, on an average, to 5£ oz.; they contain 75 per cent, of water, and the dry residue contains 45-24 per cent, of carbon, and 13-15 per cent, of ashes. 100 parts of fresh faeces consequently contain 11-31 per cent, of carbon, very nearly the same proportion as in fresh meat. In the calculation, the carbon of the faeces and of the urine has been assumed as equal to that of green vegetables, and of the food (sausages, butter, beer, &c.) consumed in the alehouse. From the observations, as recorded in the table, the following conclusions are deduced. Flesh. —Meat devoid of fat, if reckoned at 74 per cent, water, and 26 per cent, dry matter, contains in 100 parts very nearly 13-6 parts of carbon. Ordinary meat contains both fat and cellular tissue, which together amount to of the weight of the meat as bought from the butcher. The number of ounces consumed (by 855 men) was 4,448, consisting, therefore, of 3812-5 oz. of flesh, free from' fat, containing of carbon 518-5 oz. 635-5 oz. of fat and cellular tissue, ditto 449-0 oz. 4448-0 oz. In all, carbon 967-5 oz. With the bones, the meat, as purchased, contains 29 per cent, of fixed matter, including bones ; 4,448 oz. of flesh therefore contain 448 oz. of dry bones. These have not been included in the calculation, although, when boiled, they yield from 8 to 10 per cent, of gelatine, which is taken as food in the soup. Fat. —The amount of fat consumed was 56 oz.; which, the carbon being calculated at 80 per cent., contain in all 44-8 oz. of carbon. Lentils, pease and beans.— -There were consumed 53-5 oz. of lentils, 185 5 oz. of pease and 218 oz. of beans. Assuming the average amount of carbon in these vegetables to be 37 per cent., the total quantity of carbon consumed in this form was 169-1 oz. Potatoes. —100 parts of fresh potatoes contain 12-2 parts of carbon. In the 15-876 oz. of potatoes consumed, therefore, the amount of carbon was 1936-85 oz. Bread. —855 men eat daily 855 times 32 oz., besides 36 lbs. of bread in the soup, which in all amounts to 27,936 oz. 100 oz. of fresh bread contain, on an average, 3015 oz. of carbon ; consequently the carbon consumed in the bread amounts to 8771-5 oz. The total consumption, therefore, was, In the meat . . . . . . 967-50 oz. of carbon In the fat 44-80 ditto In the lentils, pease, and beans . . 16910 ditto In the potatoes 1936-85 ditto In the bread 8771-50 ditto Consumed by 855 men . . . 1188975 ditto Consumed by 1 man . . . . 13 9 ditto 84 ANIMAL CHEMISTRY. TABLE I. (to Note 3.) Containing a Summary of the Victuals consumed during November, 1840,.% a Company of the Body Guard of tlie Grand Duke of Hesse Darmstadt. ta r,h*, S :£'«f*r— *~ Beans, ta B ST period from the with food. . bles ' &c - 3kr.=ld. lbs. lbs. lbs. oz. lbs. oz. lbs. oz. lbs. oz. lbs. lbs. lbs. lbs. lbs. kr. oz. pints. 1st to 5th 139 36 9 147 0 4 15£ 3 71 — 20 12 5 4* 4 21 131 — 6th to 10th 145 37 9 165 6 — — — 16 70 71 5 3i 2l lot — 11th to 15th 136 36 9 153 2 - 3 7i - 16 42 71 41 31 2 8 — 16th to 20th 136 37 9 177 10 3 5 3 7* — 16 12 6 4* 4} 31 131 — Sau-21st to 25th 147 39 Tl 171 8 — . — 3 51 — 36 71 51 51 21 51 11 26th to 30th 152 30 19$ 177 10 3 5 3 1\ — 32 — 2* 4 3j 5? —• Total, 855 215 63 992 4 11 13 14 3 5£ 100 172 36 28 20± 15£ 56~ 1| The average f lbs. lbs. lbs. oz. oz. oz. oz. lbs. oz. lbs. lb. lb. oz. kr. oz. pint. No. of men Monthly 7# 2*f 34 13 6 T V X 7jff ljff 3 11 T V, 6 T ? T l§ ff 11 T V & Iff A daily fed is J ¦ Y/=28£, 1 oz. I|ff lb. oz. oz. oz. oz. oz. oz. lb. lb. oz. , pint, thereforeeach Daily ijh oz . 1 2 ff tffr Iff rVA Hff W Afc If* £ tt't* man had (_ T7 "r ff s** 1 • 1 1 ——¦— w N. B.—As all the weights mentioned in the text of this work are Hessian pounds and ounces, the different articles in this table have been reduced to the same weights, excepting the Pepper and Vinegar, the amount of both of which is so small that they may be omitted, without affecting the general result. For the benefit of those who may wish to reduce these weights to avoirdupois weight, it may here be mentioned, that 1 lb. Hessian=16 oz. Hessian=7680 grains Hessian=7712 grains avoirdupois. Consequently, since the 1 lb. avoirdupois is=7000 grains Troy, 1 lb. avoirdupois : 1 lb. Hessian :: 7000 : 7712, or as 1 :1-1017 j and 1 oz. Hessian=482 grains Troy (1 oz. Troy is=480 grains,) while 1 oz. avoirdupois is— 437 - 5 grains Troy. APPENDIX.—ANALYTICAL EVIDENCE. 85 The faeces of a soldier weigh 55 oz., and contain, in the fresh state, 11 per cent, of carbon. For 86 kreutzer (about 2s. 5d. sterling,) there may be bought, on an average, 172 lbs. of vegetables, such as cabbages, greens, turnips, &c. • 25 maas of sour krout weigh 100 lbs.; and for 48J kreutzer (Is. 5d. sterling,) there are brought, on an average, 24£ lbs. of onions, leeks, celery, &c* 855 men consumed Of green vegetables 2,802 oz. Of sour krout 1,600 Of onions, &c. 388 In all 4,790 And one man 5*6 oz. For this reason, the carbon of the last mentioned articles of food has been assumed as equal to that of the faaces and urine. Sausages, brandy, beer, in short, the small quantity of food taken irregularly in the alehouse, has not been included in the calculation. The daily allowance of bread, being uniformly 2 lbs. per man, with the exceptions formerly mentioned, has not been inserted in the table, which includes only those matters of which, from the daily allowance being variable, an average was required. The small quantity of bread in the table is that given in the soup, which is over and above the daily supply. NOTE (4.) See next page. NOTE (5,) p. 15. TEMPERATURE OF THE BLOOD AND FREQUENCY OF THE PULSE. According to Prevost and Dumas. The frequency The mean < • ' < temperature is of the pulse of the respiration F. in the minute. in the minute. In the Pigeon . . 107-6° . . 136 . .34 Common Fowl . 106-7 . . 140 . . 30 Duck . . . 108-5 . . 170 . . 21 Raven . . . 108-5 . . 110 . . 21 Lark . . . 117-2 . . 200 . .22 Simia Callitriche . 95-9 . . 90 . . 30 Guinea Pig . . 100-4 . . 140 . .36 Dog ... 99-3 . 90 . . 28 Cat ... 101-3 . . 100 . .24 Goat ... 102-5 . . 84 . . 24 Hare .... 1004 . . 120 . .36 Horse . . . 98-2 . 56 . . 16 Man .... 98-6 . . 72 . .18 Man(Liebig) . . 97-7° \ 65 \ . 17 Woman (Liebig) . 98-2 . . 60 . . 15 The temperature of a child is 102-2°. The temperature of the human body, in the mouth or in the rectum, for example, is from 97-7° to 98-6°. That of the blood (Majendie) is from 100-6° to 101-6°. As a mean temperature, 99 5° has been adopted in this work, page 15. NOTE (6,) p. 20. The prisoners in the house of arrest of Giessen receive daily Ij lb. of bread (24 oz.,') which contain 7i oz. of carbon. They receive, besides, 1 lb. of soup daily, .and on each alternate day, 1 lb. of potatoes. li lb. of bread contains .... 7*25 oz. of carbon. 1 lb. of soup contains 0-75 ditto. 4 lb. of potatoes contains . . . . 1*00 ditto. Total 900 ditto.f * In the original table, the quantities of these vegetables are entered according to their value in kreutzers, but they are here calculated by weight from the above data, as this appeared better adapted for comparison in this country than the prices would have been. —Ed. t At page 36 the carbon contained in the of these prisoners is calculated at 8$ oz., and ANIMAL CHEMISTRY. 86 TABLE II.—Note (4,) p. 14. a POOD CONSUMED BY A HORSE IN TWENTY-POUR HOURS. FOOD CONSUMED BY A COW IN TWENTY-FOUR HOURS. Weight Weight ' Salts I Weight Weight Salts" Articles of in the in the jb-jjjU. Hydro- Oxy- Nitro- and Articles of in the in the r . Hydro- Oxy- Nitre - and food. fresh dry. ' gen. gen. gen. earthy food. fresh dry oarDon - g en . g en . g en . earthy state. state. matters. state. state. matters. Hay 7500 6465 2961-0 323-2 2502-0 97-0 581-8 Potatoes 15000 4170 1839-0 241-9 1830-6 50-0 208-5 Oats 2270 1927 977-0 123-3 707-2 42-4 77-1 After Grass 7500 6315 2974-4 353-6 2204-0 151-5 631-5 Water 16000 — — — — — 133 Water 60000 — — — — — 50-0 Total 25770 8392 3938-Q 446-5 3209-2 139-4 672-2 Total 82500 10485 4813-4 595-5 4034-6 201-5 889-0 EXCRETIONS OF A HORSE IN TWENTY-FOUR HOURS. EXCRETIONS OF A COW IN TWENTY-FOUR HOURS. Weight Weight Salts Weight Weight : Salts - Excretions. ™ \ e in , tlae Carbon. H y dr °- °*y- Nitr0 " and Excretions. ? th * in A the Carbon. H y dr °- Nitro " and fresh dry gen. gen. gen. earthy fresh dry aiu " u - g en . g eQ> g en . earthy. state. state. matters. state. state. matters Urine 1330 302 108-7 11-5 34-1 37-8 109-9 Excrements. 28413 4000-0 1712-0 208-0 1508-0 92 0 480-0 Excrements 14250 3525 1364-4 179-8 1328-9 77-6 574-6 Urine 8200 960-8 261-4 25-0 253-7 36-5 384-2 , : — " Milk 8539 1150 6 628-2 99-0 321-0 46-0 56-4 Total 15580 3827 1472-9 191-3 1363-0 115-4 684-5 : : : Total 45152 6111-4 2601-6 332-0 2082-7 174-5 920-6 Total from , tUStf 25770 8392 39380 4465 "» 1394 6722 82500 10485-0 4813-4 595-5 4034-6 201-5 889-0 Table. this Table. Difference 10190 4565 2465-1 255-2 1846-2 24-0 12-3 Difference 37348 4374-6 2211-8 263-5 1951-9 27-0 31-6 + or— — — — — — — -f + or — — — — — — — + a Boussingault, Ann. de Ch. et de Phys., LXX., 136. The weights in this table are given in grammes. 1 gramme— =15-44 grains Troy, very nearly. APPENDIX.—ANALYTICAL EVIDENCE. 87 NOTE (7,) p. 21. COMPOSITION OF THE FIBRINE AND ALBUMEN OF BLOOD. O. Albumen from Serum of Blood. Fibrine. Scherer.* Scherer. Mulder. , A , , V , I. II. III. I. II. III. Carbon . 53850 55-461 56-097 53 671 54-454 54-56 Hydrogen . 6-983 7-201 6-880 6-878 7-069 6 90 Nitrogen . 15 673 15 673 15-681 15-763 15-762 15-72 Oxygen ~) . Sulphur S- 23-494 21-655 22-342 23 688 22715 22 82 Phosphorus j a Annalen der Chem. und Pharm., XXVIII., 74, and XL., 33, 36. For additional analyses of animal fibrine and albumen, see Note (27,) which also contains analyses of the various animal tissues. NOTE (8,) p. 22. composition op vegetable fibrine, vegetable albumen, vegetable caseine, and vegetable gluten. Vegetable fibrine. gluten, As obtained from wheat flour. ShererJones. *b Marcet.c Boussingault. i. ii. in. iv. i. ii. Carbon . 53064 54-603 54-617 53-83 55-7 53-5 Hydrogen . 7 132 7-302 7-491 7-02 14-5 150 Nitrogen 15-359 15-809 15-809 15-58 7-8 7-0 Oxygen ~) Sulphur 5- 24-445 22-285 22083 23-56 22-0 24-5 Phosphorus J b Ann. der Chem. und Pharm., XL., 7. 6 Ibid., XL., 65. c L. Gmelin's Theor. Chemie, II., 1092. VEGETABLE ALBUMEN, «. From Rye. Wheat. Gluten. Almonds. Jones.* Jones.* Varrentrapp & Will.* Jones.* Carbon . . 54-74 5501 54-85 5703 Hydrogen . 7-77 7-23 6-98 7-53 Nitrogen . 15-85 1592 1588 13-48 Oxygen ~) Sulphur 5- 21-64 21-84 2239 21-96 Phosphorus j Boussingault. Varrentrapp and Will:* Carbon . . . 52.7 Hydrogen . . 6-9 Nitrogen . . . 18 4 15 70 Oxygen, &c.. . 22 0 a Ann. der Chem. und Pharm., XL, 66, and XXXIX., 291. VEGETABLE CASEINE.CC Sulphate of Caseine and Potash. Scherer.* Jones.* Varrentrapp and Will. Carbon . . . 54-138 55-05 51-41 51-24' Hydrogen . . .7-156 7-59 7-83 6-77 Nitrogen . . • 15-672 15 89 14-48 13 23 Oxygen, &c. . . . 23-034 21-47 a Ann. der Chem. und Pharm., XXXIX., 291, and XL., 8 and 67. VEGETABLE GLUTEN. Jones. *o Boussingault. Carbon . . . 55-22 5¥? Hydrogen . . . 7-42 7-5 65 Nitrogen . . . 15-98 13-9 189 Oxygen, &c. . . . 21-38 24-4 22 3 a Ann. der Chem. und Pharm., XL., 66. The pure gluten, analyzed by Jones, was that portion of the raw gluten from wheat flour which is soluble in hot alcohol. The insoluble portion is vegetable fibrine, the analysis of which has been already given. ?he appendix in the original makes the number also 8 - 5, apparently by an error in adding up the above numbers, which yield the sum of 9 oz*. Possibly there may be an error in excess in the proportion of carbon calculated for the soup, which, in that case, ought to be 0 25 oz. —Editor. 88 ANIMAL CHEMISTRY. NOTE (9,) p. 24. COMPOSITION OP ANIMAL CASEINE.fl Scherer. x From fresh From sour From milk by Albuminous submilk, milk. acetic acid. stance in milk.6 I. ft. III. IV. V. 1 Carbon . 54-825 54-721 54 665 54-580 54-507 Hydrogen . 7-153 7-239 7-465 7-352 6-913 Nitrogen . 15-628 15-724 15-724 15-696 15-670 Sftffiil ' 22 ' 394 22 316 22 " 146 22-372 22,910 a Ann. der Chem. und Pharm., XL., 40 et seq. b This substance, called, in German, zieger, is contained in the whey of milk after coagulation by an acid. It is coagulated by heat, and very much resembles albumen. Mulder.a Carbon 54-96 Hydrogen 7-15 Nitrogen 15-89 Oxygen 21-73 Sulphur 0-36 a For the analysis of vegetable caseine, see the preceding note. NOTE (10,) p. 27. AMOUNT OF MATTER SOLUBLE IN ALCOHOL IN THE SOLID EXCREMENTS OF THE HORSE AND COW. (WILL.*) 18*3 grammes of dried horse-dung lost, by the action of alcohol, 0-995 gramme. The residue, wnen dry, had the appearance of saw-dust, after it had been deprived, by boiling, of all soluble matter. 14-98 grammes of dry cow-dung lost, by the same treatment, 0*625 gramme. NOTE (11,) p. 28. COMPOSITION OF STARCH. 0 Strecker.* Calculated From From From From C12H10O10. Peas. Lentils. Beans. Buckwheat. Carbon . . 44.91 44-33 44-46 44-16 44-23 Hydrogen . .6-11 6 57 6-54 6-69 6-40 Oxygen . . 4898 49-09 49-00 4915 49-37 Strecker.* f rom maize. From horse-chestnuts. From wheat. From rye. < I Carbon . . . 44-27 44-44 44-26 44-16 Hydrogen . 667 6-47 670 6-64 Oxygen . . 49-06 4908 49 04 4920 Strecker.* * From From From .» From rice. dahlia-roots. unripe apples, unripe pears. Carbon . . 44-69 4413 44-10 44-14 Hydrogen . . 6-36 6-56 6-57 6-75 Oxygen . . 48 95 49-31 49-33 49-11 From potatoes. From arrow-root. From yams.a Berzelius. Gay Lussac & Thenard. Prout. Ortigosa, Carbon . 44-250 43-55 44-40 44-2 Hydrogen . 6-674 6-77 6-18 6-5 Oxygen . 49076 . 49-68 4942 49-3 a The starch employed for the analyses, made by Strecker and Ortigosa, was prepared from the chemical laboratory at Giessen, from the respective seeds, bulbs, and fruits. NOTE (12,) p. 28. COMPOSITION OP GRAPE SUGAR. (STARCH SUGAR.) From grapes.a From starch. b From honey.c Calculated. De Saussure. Prout. C12H14014. Carbon . 36-71 37-29 36-36 36-80 Hydrogen . 6-78 6-84 7-09 7-01 Oxygen . 56-51 5587 56-55 56-19 a Ann. de Chimie, XI., 331. 6 Ann. of Philosophy, VI., 426. c Philosoph. Trans. 1827,373. APPENDIX.—ANALYTICAL EVIDENCE. 89 NOTE (13,) p. 29. COMPOSITION OP SUGAR OP MILK. GayLussac , Calculated and Thenard. Prout. Brunn. Berzelius. Liebir.* C12H13012. Carbon . 38-825 40-00 40-437 39-474 40 00 40-46 Hydrogen 7-341 666 6711 7-167 673 6-61 Oxygen. 53-834 53-34 52-852 53-359 53.27 52-93 NOTE (14,) p. 29. COMPOSITION OP GUM. Gay Lussac Calculated, and Thenard. Goebcl. Berzelius. C12H11011. Carbon • 42*23 42*2 42682 42-58 Hydrogen 6-93 6 6 6 374 6 37 Oxygen ¦ 50 84 51*2 50*944 51*05 NOTE (15,) p. 29. ANALYSIS OP OATS. (Boussingault.) O. 100 parts of oats contain of dry matter . . . 82*9 Ditto water . . . .17-1 1000 100 parts of oats dried at 212° —1177 parts dried at the ordinary temperature, contain Carbon . . 50*7 Hydrogen . . 6*4 Oxygen . . 36-7 Nitrogen . . 2-2 Ashes . . 4*0 100*0 Water . . . 177 Oats dried in the air 1177 contain, in 100 parts, 1-867 of nitrogen. a Ann. de Chimie et de Phys., LXXI., 130. ANALYSIS OP HAY. 100 parts of hay dried in the air contain 86 of dry matter, 14 of water. 100 100 parts of hay dried at 212°=» 116 2 parts dried in air, contain Carbon . . 45-8 Hydrogen . . 50 Oxygen . . 387 Nitrogen . . 1-5 Ashes . ... 90 100-0 16-2 water, 116-2 hay dried in the air. 100*0 of hay dried at the ordinary temperature contain 1-29 of nitrogen. 240 oz. of such hay=15 lbs. contain . . 3-095 oz. of nitrogen. 72 oz. of oats =4J lbs. contain , 1*34 ditto Total . . . 4*435 ditto NOTE (16,) a, p. 30. AMOUNT OP CARBON IN FLESH AND IN STARCH. 100 parts of starch contain 44 of carbon j therefore, 64 oz. (4 lbs.) contain 28*16 oz. of carbon. 100 parts of fresh meat contain 13-6 of carbon (see Note III.;) hence 240 oz. (15 lbs.) contain 32-64 oz. of carbon.* * By an error in calculation in the original, the amount of carbon in 15 lbs. of meat is stated to be 27*64 oz. It follows, that the carbon of 4 lbs. of starch is not equal, as stated in the text, to that of 15 lbs. of flesh, but to that of 13 lbs. This difference, however, is not sufficient to affect the argument at p. 32. —Editor. 12 H 90 ANIMAL CHEMISTRY. NOTE (16,) b, p. 32. COMPOSITION OP Hog's Lard. Mutton fat. Human fat. Chevreul. a Carbon . . .79-098 78-996 79000* Hydrogen . . 11-146 11700 11-416 Oxygen . . . 9-756 . 9-304 9-584 a Recherches Chim., sur les Corps Gras. Paris. 1823. NOTE (17,) p. 32 COMPOSITION OF CANE STTGAB. According to Berzelius. Prout. W.Crun, Liebig. jftgg* ggjgfc Carbon 42-225 42-86 42-14 42-301 42-47 42-58 Hydrogen 6-600 6-35 6-42 6-384 6-90 6-37 Oxygen 51-175 50-79 51-44 51-315 5063 51-05 For the composition of gum and of starch, see Notes (14) and (11) NOTE (18,) p. 32. COMPOSITION OP CHOLESTERINE. According to Chevreul. a Coueroe. 6 Marchand. Calculated C36H320. Carbon . . 85-095 84-895 84-90 84-641 Hydrogen . 11-880 12-099 12-00 12-282 Oxygen . . 3-025 3-006 3-10 3-077 a Recherches sur les Corps Gras, p. 185. b Ann. de Ch. et de Phys. LVI., p. 164. NOTE (19,) p. 33. THE PRODUCTION OF WAX FROM SUGAR.* As soon as the bees have filled their stomach, or what is called the honey bladder, with honey, and cannot deposit it for want of cells, the honey passes gradually in large quantity into the intestinal canal, where it is digested. The greater part is expelled as excrement ; the rest enters the fluids of the bee. In consequence of this great flow of juices a fatty substance is produced, which oozes out on the eight spots formerly mentioned, which occur on the four lower scales of the abdominal rings, and soon hardens into laminae of wax. On the other hand, when the bees can deposit their honey, only so much enters the intestinal canal as is necessary for their support. The honey bladder need not be filled with honey longer than forty hours in order to bring to maturity, on the eight spots, eight lamina? of wax, so that the latter fall off. I made the experiment of giving to bees, which I had enclosed in a box with their queen about the end of September, dissolved sugar candy instead of honey. Out of this food laminae of wax were formed ; but these would not separate and fall off readily, so that the mass, which continued to ooze out, remained, in most of the bees, hanging to the upper laminae: and the laminae of wax became as thick as four under ordinary circumstances. The abdominal scales of the bees were, by means of the wax, distinctly raised, so that the waxen laminae projected between them. On examination, I found that these thick laminae, which under the microscope exhibited several lamellae, had a sloping surface downwards near the head, and upwards in the vicinity of the tail. The first waxen laminae, therefore, must have been pushed downwards by the second, because, where the abdominal scales are attached to the skin, there is no space for two laminae, the second by the third, and thus the inclined surfaces on the sid«s of the thick laminae had been produced. I saw distinctly from this, that the first formed laminae are detached by those which followed. The sugar had been converted into wax by the bees, but it would seem that there was some imperfection in the process, as the laminae did not fall off, but adhered to the succeeding ones. In order to produce wax in the manner described, the bees require no pollen, but only honey. I have placed, even in October, bees in an empty hive, and fed them with honey; they soon formed comb, although the weather was such that they could not leave the hive. I cannot, therefore, believe that pollen furnishes food for the bees, but I think they only swallow it, in order, by mixing it with honey and water, to prepare the liquid food for the grubs. Besides, bees often starve in April, when their stock, of honey is consumed, and when they can obtain in the fields abundance of pollen, but no honey. * From F. W. Gundlach's Natural History of Bees, p. 115. Cassel, 1842 We are acquainted with no more beautiful or convincing proof of the formation of fatty matter from sugar than the following process of the manufacture of wax by the bees, as taken from observation. APPENDIX—ANALYTICAL EVIDENCE. 91 When pressed by hunger they tear the nymphae out of the cells, and gnaw them in order to support life by the sweet juice which they contain. But, if in this condition they are not artificially fed, or if the fields do not soon yield their proper food, they die in the course of a few days. Now, if the pollen were really nourishment for bees, they ought to be able to support life on it, mixed with water. - • Bees never build honeycomb unless they have a queen, or are provided with young out of which they can educate a queen. But if bees be shut up in a hive without a queen, and fed with honey, we can perceive in forty-eight hours that they have laminae of wax on their scales, and that some have even separated. The building of cells is therefore voluntary, and dependent on certain conditions, but the oozing out of wax is involuntary. One might suppose that a large proportion of these laminae must be lost, since the bees may allow them to fall off, out of the hive as well as in it; but the Creator has wisely provided against such, a loss. If we give to bees engaged in building cells honey in a flat dish, and cover the dish with perforated paper, that the bees may not be entangled in the honey, we shall find, after a day, that the honey has disappeared, and that a large number of laminae are lying on the paper. It would appear as if the bees, which have carried off the honey, had let fall the scales; but it is not so. For, if above the paper we lay two small rods, and on these a board, overhanging the dish on every side, so that the bees can creep under the board and obtain the honey, we shall find next day the honey gone, but no laminae on the paper; while laminae will be found in abundance on the board above. The bees, therefore, which go for and bring the honey, do not let fall the laminae of wax, but only those bees which remain hanging to the top of the hive. Repeated experiments of this kind have convinced me that the bees, as soon as their laminae of wax are mature, return to the hive and remain at rest, just as caterpillars do, when about to change. In a swarm that is actively employed in building we may see thousands of bees hanging idly at the top of the hive. These are all bees whose laminae of wax are about to separate. When they have fallen off, the activity of the bee revives, and its place is occupied for the same purpose by another. (From page 28 of the same work.) In order to ascertain how much honey bees require to form wax, and how often, in a swarm engaged in building, the laminae attain maturity and fall off, I made the following experiment, which appears to me not uninteresting. On the 29th of August, 1841, at a time when the bees could obtain in this district no farther supply of honey from the fields, I emptied a small hive, placed the bees in a small wooden hive, having first selected the queen bee, and shut her up in a box, furnished with wires, which I placed in the only door of the hive, so that no embryoes could enter the cells. I then placed the hive in a window, that I might be able to watch it. At 6 p. m. I gave the bees 6 oz. of honey run from the closed cells, which had thus the exact consistence of freshly made honey. This had disappeared next morning. In the evening of the 30th I gave the bees 6 oz. more, which, in like manner, was removed by the next morning; but already some laminae of wax were seen lying on the paper with which the honey was covered. On the 31st August and the 1st September the bees had in the evening 10 oz., and on the 3d of September in the evening 7 oz.; in all, therefore, 1 lb. 13 oz. of honey, which had run cold out of cells which the bees had already closed. On the 5th of September I stupified the bees, by means of puff-ball and counted them. Their number was 2,765, and they weighed 10 oz. I next weighed the hive, the combs of which were well filled with honey, but the cells not yet. closed ; noted the weight, and then allowed the honey to be carried off by a strong swarm of bees. This was completely effected in a few hours. I now weighed it a second time, and found it 12 oz. lighter; consequently the bees still had in the hive 12 oz. of the 29 oz. of honey given to them. I next extracted the combs, and found that their weight was £ of an ounce. I then placed the bees in another box, provided with empty combs, and fed them with the same honey as before. In the first few days they lost daily rather more than 1 oz. in weight, and afterwards half an ounce daily, which was owing to the circumstance, that from the digestion of so much honey, their intestinal canal was loaded with excrements; for 1,170 bees, in autumn, when they have been but a short time confined to the hive, weigh 4 oz.; consequently 2,765 bees should weigh 9 oz. But they actually weighed 10 oz., and therefore had within them 1 oz. of excrement, for their honey bladders were empty. During the night the weight of the box did not diminish at all, because the small quantity of honey the bees had deposited in the cells, having already the proper consistence, could not lose weight by evaporation, and because the bees could not then get rid of their excrements. For this reason, the loss of weight occurred always during the day. If, then, the bees, in seven days, required 3_ oz. of honey to support and nourish their bodies, they must have consumed 13_ oz. of honey in forming $• of an ounce of wax; and consequently, to form 1 lb. of wax, 20 lbs. of honey are required. This is the reason why the strongest swarms in the best honey seasons, when other hives, that have no occasion to build, often gain in one day 3 or 4 lbs. in weight,,hardly become heavier, although their activity is boundless. All that they gain is expended in making wax. 92 ANIMAL CHEMISTRY. This is a hint for those who keep bees, to limit the building of comb. Cnauf has already recommended this, although he was not acquainted with the true relations of the subject. From 1 oz. of wax, bees can build cells enough to contain 1 lb. of honey. 100 lamina; of wax weigh 0-024 gramme (rather more than of a grain,) consequently, 1 kilogramme (=» 15,360 grains) will contain 4,166,666 laminae. Hence, £ of an ounce will contain 81,367 laminae. Now this quantity was produced by 2,765 bees in six days; so that the bee requires for the formation of its 8 laminae (one crop) about thirty-eight hours, which agrees very well with my observations. The laminae, when formed, are as white as bleached wax. The cells also, at first, are quite white, but they are coloured yellow by the honey, and still more by the pollen. When the cold weather comes on, the bees retire to the hive under the honey, and live on the stock they have accumulated. P. 54. Many believe that bees are hybernating animals; but the opinion is quite erroneous. They are lively throughout the winter; and the hive is always warm in consequence of the heat which they generate. The more numerous the bees in a hive, the more heat is developed ; and hence strong hives can resist the most intense cold. It once happened that I forgot to remove from the door, which was unusually large, of a hive in winter, a perforated plate of tinned iron, which I had fastened over the opening to diminish the heat in July; and yet this hive came well through the winter, although the cold was very severe, having been for several days so low as 0°. But I had added to this hive the bees of two other hives! When the cold is very intense, the bees begin to hum. By this means respiration is accelerated and the developement of heat increased. If, in summer, bees without a queen are shut up in a glass box, they become uneasy and begin to hum. So much heat is by this means developed, that the plates of glass become quite hot. If the door be not opened in this case, or if air be not admitted, and if the glass be not cooled by the aid of water, the bees are soon suffocated. COMPOSITION OF BEES 5 WAX. Gay Lussac Calculated and Thenard.a De Saussure.5 Oppermann.c Ettling.d Hess.e C20H20O. Carbon . 81-784 81-607 81-291 81-15 81 52 81-38 Hydrogen . 12-672 13.859 14073 1375 1323 1328 Oxygen . 5-544 4-534 4-636 5 09 5-25 5 34 a Traite de Chimie, par M. Thenard, 6me- Ed. TV., 477. b Ann. de Ch. et de Phys. XIII., 310. c Ibid. XLIX., 224. d Annal. der Pharm., II., 267. e Ibid. XXVII., 6. NOTE (21) a, p. 36. COMPOSITION OP HYDRATED CYANURIC ACID, OR HYDRATED CYANIC ACID, AND OP CYAMELIDE, IN 100 PARTS, ACCORDING TO THE ANALYSIS OP W6HLER AND LIEBIG.*'rt Cyanuric acid, cyanic acid, cyamclide. Carbon 2819 Hydrogen 230 Nitrogen 3263 Oxygen 36-87 a Poggendorff's Annalen, XX., 375 etseq. NOTE (21) b. p. 36. COMPOSITION OP ALDEHYDE, METALDEHYDE, AND ELALDEHYDE.lt Aldehyde. Metaldehyde. Elaldehyde. Calculated Liebig.* Fehling.* C4H402. Carbon . 55,024 ' 54-511- 54-467 ' 55-024 Hydrogen . 8983 9 054 9 248 9 075 8-983 Oxygen . 35-993 36-435 36-132 36-458 35993 a Ann. der Pharm., XIV., 142, und XXVII., 319. NOTE (22,) p. 37. COMPOSITION OF PROTEINE. From the crystalline lens. From albumen. From fibrine. Scherer.a Carbon . . 55-300 55-100 54-848' Hydrogen . . 6940 7-055 6-959 Nitrogen . . 16-216 15966 15 847 Oxygen . . . 21-544 21-819 22 346 * a Ann. der Chem. und Pharm., XL., 43. APPENDIX.—ANALYTICAL EVIDENCE. 93 Scherer.a , * > Calculated From hair. From horn. C48H36N6014. Carbon . . . 54-746 55150 55-408 54-291* 55-742 Hydrogen . . . 7-129 7-197 7-238 7-082 6-827 Nitrogen . . 1-727 15-727 15593 15-593 16143 Oxygen . . . 22-398 21-926 21-761 23034 21-228 a Ann. der Chem. und Pharm., XL;, 43. From vegetable albumen. From fibrine. From albumen. From cheese. Mulder.o Carbon .... 54-99 55-44 55159 Hydrogen .... 6-87 8-95 6-94 7176 Nitrogen . . . 15-66 1605 16-02 15-857 Oxygen .... 22-48 21-56 21-74 21-808 a Ann. de Pharm., XXVIII., 75. NOTE (23,) p. 37. COMPOSITION OF THE ALBUMEN OF THE YOLK AND OF THE WHITE OF THE EGG.a From the yolk. From the white. Jones.* Scherer.* Carbon . . 53-72 53-45 55-000 Hydrogen . . 7-55 766 7-073 Nitrogen . . 13-60 1334 15-920 Oxygen Sulphur £ . 25-13 25-55 22-007 Phosphorus J a Ann. der Chem. und Pharm. XL., 36, ibid. 67. NOTE (24,) p. 38. COMPOSITION OF LACTIC ACID. C6H505, Carbon 4490 Hydrogen 6-11 Oxygen 48-99 NOTE (25,) p. 39. OAS FROM THE ABDOMEN OF COWS AFTER EATING CLOVER TO EXCESS, OBTAINED BY PUNCTURE. a Examined by Lameyran and Fremy. b By Vogel. c By Pflugtj. Air. Carbonic acid. Inflammable gas. Sulphuretted hydrogen. a 5 , 5 — 15 80 Vol. in 100 Vol. b 25 — 27 48 — c — — 60 40 — c — — 20 80 — NOTE (26,) p. 40. M AGENDIE FOUND IN THE STOMACH AND INTESTINES OF EXECUTED CRIMINALS : a In the case of an individual who had taken food in moderation one hour previous to death; b, in the case of one who had done so two hours previously; and c, in the case of a third, who had done so four hours previous to execution. 100 Volumes of the gas contained: Oxygen. Nitrogen. Carbonic acid. Inflammable gas. ("From the stomach 11 -00 Vol. 71-45 14-00 3-55 — small intestines 00 00 20-03 24-39 55-53 t — large intestines 00 00 51-03 43-50 5-47 TFrom the stomach 00-00 00-00 00 00 00-00 bl — small intestines 00-00 8-85 40 00 51-15 t — large intestines 00-00 18-40 70 00 11-60 TFrom the stomach 00 00 00-00 00-00 00-00 c< — small intestines 00 00 66-60 25 00 8-40 t — large intestines 00-00 45 96 42 86 11-18 94 ANIMAL CHEMISTRY. NOTE (27,) referred to in NOTE (7,) p. 21. COMPOSITION OP ANIMAL ALBUMEN AND FIBRINE, AND OF THE DIFFERENT TISSUES OF THE BODY. 1. ALBUMEN. From the serum of blood. From eggs. From yolk of egg. Scherer. *a Jones. *b I. II. III. IV. V. VI. Carbon . 53-850 55-461 55097 55-000 53-72 53-45 Hydrogen . 6-983 7-201 6-880 7-073 7.55 7-66 Nitrogen . 15673 15-673 15-681 15-920 13-60 13-34 Oxygen ~) Sulphur S- 23-494 21-655 22-342 ¦ 22-007 25-13 25-55 Phosphorus 3 a Ann. der Chem. und Pharm., XL., 36. b Ibid. 67. Jones.* Scherer.* t * < From albumen From From congestive From fluid of brain. hydrocele. abscess. From pus. of dropsy. vir. vnr. ix. x. xi. in Carbon . . 55-50 54-921 54-757 54-663 54-101 54-302 Hydrogen . . 7-19 7 077 7-177 7-022 6-947 7-176 Nitrogen . 16-31 15-465 15-848 15839 15-660 15-717 Oxygen ~) Sulphur £ . 21-00 22-537 22-224 22-476 23-292 22-805 Phosphorus _) • Mulder.a Carbon ' 54-84 Hydrogen 7-09 Nitrogen ' 15*83 Oxygen . . . . . . 21*23 Sulphur • 0*68 Phosphorus 0*33 a Ann. der Pharm. XXVIIL, 74. 2. Fibrine. Scherer.*a ' I. II. - III. IV. . V. VL VII. ' Carbon 53*671 54.454 55*002 54*967 53*571 54-686 54-844 Hydrogen 6-878 7-069 7-216 6-867. 6-895 6-835 7-219 Nitrogen 15-763 15-762 15-817 15-913 15-720 15-720 16-065 Oxygen "} Sulphur 23-688 22-715 21*965 22*244 23*814 22*759 21*872 Phosphorus j » a Ann. der Chem. und Pharm., XL., 33. Carbon .... 54*56 Hydrogen . . . . 6-90 Nitrogen .... 15.72 Oxygen . . . .22-13 Sulphur .... 0-33 Phosphorus .... 0-36 a Ann. der Chem. und Pharm., XXVIIL, 74. 3. Gelatinous Tissues. Scherer.*a Isinglass. Tendons of the Tunica Calculated. calf's foot. sclerotica. C48H41N7J018 Carbon 50*557 49*563 50-960 50-774' 50*995 50-207 Hydrogen 6-903 7-148 7-188 7-152 7-075 7-001 Nitrogen 18-790 18-470 18-320 18-320 18-723 18-170 Oxygen 23750 24.819 23-532 23754 23207 24 622 a Ann. der Chem. und Pharm., XL., 46. Mulder. Carbon . . . 50 048 50-048 Hydrogen . . . 6*477 6*643 Nitrogen . . . 18*350 18*388 Oxygen . . . 25*125 24*921 APPENDIX—ANALYTICAL EVIDENCE. 95 4. Tissues containing Chondrine. Scherer. *o Cartilages of the Calculated ribs of the calf. Cornea. C48H40N6O20 Mulder. Carbon 49-496 50-895 49-522 50-745 ' 50-607 Hydrogen 7-133 6-962 7-097 6-904 6-578 Nitrogen 41-908 14-908 14-399 14-692 14-437 Oxygen 28-463 27-235 28-982 27-659 28-378 a Ann. der Chem. und Pharm., XL., 49. 5. Composition of the Middle Membrane of Arteries. Scherer.*a , » » Calculated t II. C48H38N6016 Carbon 53-750 53393 5391 Hydrogen 7-079 6-973 6-96 Nitrogen 15-360 15 360 15 60 Oxygen 23-811 24-274 23-53 a Ann. der Chem. und Pharm., XL., 51. 6. Composition of Horny Tissues. Scherer. *a External skin Hair of Hair of the head, of the sole of the foot, the beard. Fair. Brown. Black. Carbon 51-036 50-752 51-529 50-652 49-345 50-622 49-935 Hydrogen 6-801 6-761 6-687 6-769 6-576 6-613 6-631 Nitrogen 17-225 17-225 17-936 17-936 17-936 17-936 17-936 Suffitrl" 24-938 25-262 23-848 24-643 26-143 24-829 25-498 Scherer.*a * » , Calculated Buflalohorn. Nails. Wool. C48H39N7017 Carbon 51-990 51-162 "5T620~51-546 51-089 50-653 51-718 Hydrogen 6-717 6-597 6-754 6-779 6-824 7-029 6-860 Nitrogen 17-284 17-284 17-284 17-284 16-901 17-710 17-469 Suffiur} 24-009 24-957 24-342 24-397 25-186 24,608 23953 a Ann. der Chem. und Pharm., XL., 53. The composition of the membrane lining the interior of the shell of the egg approaches closely to that of horn. According to Scherer, it contains Scherer. *a Carbon 50;674 Hydrogen . . . . . . 6'608 Nitrogen 16-761 2 x 7f n i . . . . . .25-958 Sulphur ) a Ann. der Chem. und Pharm., XL., 60. The composition of feathers is also nearly the same as that of horn. Scherer.*a Beard of the Quill of the Calculated feather. feather. C4SH39N7016. Carbon . . 50434 52-427 52-457 Hydrogen . . 7-110 7-213 6-958 Nitrogen . . 17-682 17-893 17-719 Oxygen . . . 24-774 22-467 22-866 a Ann. der Chem. und Pharm., XL., 61. The analysis here given of the beard of feathers agrees closely with that of horn, while that of the quill is more accurately represented by the attached-formula, which diners from that-of horn by 1 eq. of oxygen only. 7. Composition of the Pigmentum Nigrum Oculi. Scherer.*o Carbon . . . 58-273 5?673 57-908 Hydrogen . . . 5973 5 962 5-817 Nitrogen ... 13-768 13768 13-768 Oxygen . . . 21-986 21-598 22-507 a Ann. der Chem. und Pharm., XL., 63. 96 ANIMAL CHEMISTRY. NOTE (28,) p. 44. According to the analyses of Playfair and Boeckmann, 0-452 parts of dry muscular flesh gave 0 836 of carbonic acid. 0-407 0-279 of water. 0-242 ...... 0-450 of carb. acid and 0-164 water. 0191 0-360 . . . 0-130 0-305 of dried blood gave 0 575 carbonic acid and 0-202 of water. 0-214 . . . 0-402 . . . 0-138 I 1-471 of dried blood, when calcined, left 0-065 of ashes=4-42 pr. cent. The dried flesh was found to contain of ashes 4-23 pr. cent. 'The nitrogen was found to be to the carbon as 1 to 8 in equivalents. Hence Flesh (beef.) Ox-blood. Blood. Playfair. Boeckmann. Playfair. Boeckmann. Mean of 2 analyses. Carbon 51-83 51-89 51-95 51'-96 51-96 Hydrogen 7-57 7-59 7-17 7-33 7-25 Nitrogen 1501 15-05 15-07 1508 1507 Oxygen 21-37 21-24 2139 21-21 21-30 Ashes 4-23 4-23 4-42 4-42 4-42 Deducting the ashes, or inorganic matter, the composition of the organic part is, Carbon . . . 54-12 54-18 54-19 54-20 Hydrogen . . . 7-89 7-93 7-48 7-65 Nitrogen . . 15-67 15-71 15-72 15-73 Oxygen . . . 22-32 22-18 22-31 22-12 This corresponds to the formula C 48 54-62 H 39 7-24 N« 15-81 ' O w ...... 22-33 NOTE (29,) p. 44. COMPOSITION OF CHOLEIC ACID, tt Calculated Demarcay. Dumas. C76H66N2022. Carbon . . 63-707 63 5 63-24 Hydrogen . . 8 821 9 3 8-97 Nitrogen . . 3-255 3-3 3-86 Oxygen . . 24.217 23-9 23-95 a Ann. der Pharm., XXVII., 284 and 293. NOTE (30,) p. 44. COMPOSITION OF TAURINE AND OF CHOLOIDIC ACID. 1. Taurine, a Calculated. Demargay.* Dumas. C4H7NO!0 Carbon . . 1924 1926 1948 Hydrogen . . 5-78 5-66 5-57 Nitrogen . .11-29 11.19 11-27 Oxygen . . 63-69 63-89 63-68 a Ann. der Pharm., XXVII., 287 and 292. 2. Choloidic Acid, a Demargay.* A Dumas. Calculated. 'J ; Ij 1 C36H56012 Carbon . . 73-301 73-522 73-3 74-4 Hydrogen ' . 9-511 9-577 9-7 94 Oxygen . . 17-188 16901 17-0 162 a Ann. der Pharm., XXVII., 289 and 293. In reference to the researches of Demarcay on the bile I would make the following observations. The matter to which I have given the name of choleic acid is the bile itself separated from the inorganic constituents (salts, soda, &c.) which it contains. By the action of subacetate of lead aided by ammonia, all the organic constituents of the bile are made to unite with oxide of lead, with which they form an insoluble, resinous precipitate. The APPENDIX.—ANALYTICAL EVIDENCE. 97 substance here combined with oxide of lead contains all the carbon and nitrogen of the bile. The substance which I have named choloidic acid is that which is obtained, when the bile, purified by alcohol from the substances insoluble in that fluid, is boiled for some time with an excess of muriatic acid. It contains all the carbon and hydrogen of the bile, except those portion which have separated in the form of taurine and ammonia. The cholic acid contains the elements of bile, minus those of carbonate of ammonia. These three compounds, therefore, contain the products of the metamorphosis of the entire bile; their formulae express the amount of the elements of the constituents of the bile. No one of them exists ready formed in the bile in the shape in which we obtajn it; their elements are combined in a different way from that in which they were united m the bile; but the way in which these elements are arranged has not the slightesf inflence on the determination by analysis of the relative proportions of the elements. In the formula themselves, therefore, is involved no hypothesis; they are simply expressions of the results of analysis. It signifies nothing that the choleic or choloidic acids may be composed of several compounds united together. No matter how many such they may contain, the relative proportions of all the elements taken together is expressed by the formula which is derived from the analysis. The study of the products which are produced from the bile by the action of the atmosphere, or of chemical re-agents, may be of importance in reference to certain pathological conditions; but except as concerns the general character of the bile, the knowledge of these products is of no value to the physiologist; it is only a burthen which impedes his progress. It cannot be maintained of any one of the 38 or 40 substances, into which the bile has been divided or split up, that it exists ready formed in the healthy secretion; on the contrary, we know with certainty that most of them are mere products of the action of the re-agents which are made to act on the bile. The bile contains soda; but it is a most remarkable and singular compound of soda. When we cause that part of the bile which dissolves in alcohol (which contains nearly the organic part) to combine with oxide of lead, thus separating the soda, and then i move the oxide of lead, we obtain a substance, choleic acid, which, when placed in contact with soda, forms a compound similar to bile in its taste; but it is no longer bile; for bile may be mixed with organic acids, nay, even with dilute mineral acids, without becoming turbid or yielding a precipitate; while the new compound, choleate of soda, is decomposed by the feeblest acids, the whole of the choleic acid being separated. Hence, bile cannot be considered, in any sense, as choleate of soda. Further, it may be asked, in what form are the cholesterine, and stearic, and margaric acids, which are found in bile, contained in that fluid 1 Cholesterine is insoluble in water, and not saponifiable by alkalies; and if the two fatty acids just named were really present in the bile as soaps of soda, they would be instantly separated by other acids. Yet diluted acids cause no such separation of stearic and margaric acids in bile. It is possible that, in the course of new and repeated investigations, the composition of the substances obtained from bile may be found different from that which has been given in our analytical developement of this subject. But this, if it should happen, can have but little effect on our formulae; if the relative proportions of carbon and nitrogen be not changed, the differences will be confined to the proportions of oxygen and hydrogen. In that case it will be necessary for the developement of our views in formulae, only to assume that more water and oxygen, or less water and oxygen, have taken a share in the metamorphosis of the tissues; but the truth of the developement of the process itself will not be by this means affected. NOTE (31,) p. 44. COMPOSITION OF CHOLIC ACID, d Dumas. Calculated C74H60O18. Carbon . . . .68-5 . . .68-9 Hydrogen ... 9.7 . . 9.2 Oxygen .... 21.8 . . . 21.9 a Ann. der Pharm. XXVII., 295. NOTE (32,) p. 45. COMPOSITION OF THE CHIEF CONSTITUENTS OF THE URINE OF MEN AND ANIMALS. 1. Uric Acid. Liebig.*a Mitscherlich.6 Calculated C10H4N4O6. Carbon . . 36083 3582 36-00 Hydrogen . . 2-441 238 236 Nitrogen . . 33-361 34-60 33.37 Oxygen . . 28.126 27-20 28-27 AS a Ann. der Pharm., X., 47. b Poggendorff's Ann., XXXIIL, 335. 13 98 ANIMAL CHEMISTRY. 2. Alloxan, a A PRODUCT OF THE OXIDATION OF URIC ACID. Wcehler and Liebig.* Calculated C8H4N2O10, i A S Carbon. . . 30-38 30-18 30-34 Hydrogen . . 2-57 2-48 2-47 Nitrogen . . 17.96 17-96 17-55 Oxygen . . 4909 49-38 49.64 a Ann. der Pharm., XXVI., 260. 3. Urea. Prout. a Wcehler and Liebig. & Calculated C2H4N202 Carbon . . 19-99 20-02 20-192 Hydrogen . 6-65 6-71 6-595 Nitrogen . . 46-65 46-73 46-782 Oxygen . 26-63 26-54 26-425 a Thompson's Annals., XI., 352. 6 Poggend. Ann., XX., 375. 4. Crystallized Hippuric Acid. Liebig.* a Dumas, b Mitscherlich. c Calculated C18H8N05. Carbon 60-742 60-5 60-63 60-76 Hydrogen 4-959 4-9 4-98 4-92 Nitrogen 7-816 7-7 7-90 7-82 Oxygen 26-483 26-9 26-49 26-50 a Ann. der Pharm., XII., 20. 6 Ann. de Ch. et de Phys., LVIL, 327. c Poggend. Ann., XXXIII., 335. 5. Allantoine. a Wcehler and Liebig.* Calculated C8H6N406 Carbon .... 30.60 30 66 Hydrogen . . . 3 83 375 Nitrogen . . . 35-45 35-50 Oxygen . . . 30-12 30-09 a Ann. der Pharm., XXVI., 215. 6. Uric on Xanthic Oxide, a Wcehler and Liebig.* Calculated C5H2N202. Carbon . . . •. 39-28 39-86 Hydrogen. .. . . 2-95 2-60 Nitrogen . . . 36-35 37-72 Oxygen .... 21-24 20 82 a Ann. der Pharm., XXVI., 344. 7. Cystic Oxide, a Thaulow.* Calculated C6H6N0484. - Carbon .... 3001 30-31 Hydrogen ... 5-10 4-94 Nitrogen ... 11-00 11-70 Oxygen. . . . 2838 26-47 Sulphur .... 25-51 26-58 a Ann der Pharm., XXVII., 200. APPENDIX.—ANALYTICAL EVIDENCE. 99 The cystic oxide is distinguished from all the other concretions occurring in the urinary bladder by the sulphur it contains. It can be shown with certainty, that the sulphur is present neither in the oxidized state, nor in combination with cyanogen; and in regard to its origin the remark is not without interest, that four atoms of cystic oxide contain the elements of uric acid; benzoic acid, sulphuretted hydrogen, and water; all of which are substances, the occurrence of which in the body is beyond all doubt 1 atom uric acid . . . C 10 N 4 H 4 O 6 1 atom benzoic acid C 14 H 6 0 3 8 atoms sulphuret- ? tjs «8 ted hydrogen. . . J no 7 atoms water H 7 0 7 4 atoms cystic oxide = C"N 4 H"0 16 S 8 =4 (C 6 NH 6 0 4 S 2 ). An excellent method of detecting the presence of cystic oxide in calculi or gravel is the following: The calculus is dissolved in a strong solution of caustic potash, and to the solution is added so much of a solution of acetate of lead, that all the oxide of lead is retained in solution. "When this mixture is boiled there is formed a black precipitate of sulphuret of lead, which gives to the liquid the aspect of ink. Abundance of ammonia is also disengaged ; and the alkaline fluid is found to contain, among other products, oxalic acid. NOTE (33,) p. 45. COMPOSITION OF OXALIC, OXALITKIC, AND PARABANIC ACIDS. 1. Oxalic Acid (hydrated.) Calculated Gay Lussac & Thenard. Berthollet. C2 03-f-HO Carbon . . 26566 25-13 2666 Hydrogen . . 2-745 3-09 222 Oxygen, . . 70-689 71-78 71-12 2. Oxaluric Acid, o Wcehler and Liebig.* Calculated , < . C6H4N208 Carbon . . 27-600 27-318 27-59 Hydrogen . • 3-122 3-072 300 Nitrogen . . 21-218 21-218 21-29 Oxygen . . 48-060 48-392 48-12 a Ann. der Pharm., XXVI., 286. 3. Parabanic Acid, a Wcehler and Liebig.* Carbon . '31-95 31 -940 31-91 Hydrogen . 2 09 1-876 1-73 Nitrogen . 24-66 24-650 24-62 Oxygen . . 41-30 41-534 41 74 a Ann. de Pharm., XXVI., 286. NOTE (34,) p. 45. COMPOSITION OP ROASTED FLESH. (1.) 0-307 of flesh gave 0-584 of carbonic acid and 0 206 of water. (2.) 0-255 do. 0-485 do. 0-181 do. (3.) 0-179 do. 0-340 do. 0-125 do. Hence— Flesh of roedeer(l.) Flesh of Beef (2.) Flesh of veal (3.) Bceckmann.* Playfair. Carbon . . 52-60 52-590 42-52 Hydrogen . . . 7-45 7-886 7-87 Nitrogen . . 15 23 15-214 14-70 aXST} • • • 24,72 24,310 24,91 ANIMAL CHEMISTRY. 100 NOTE (35,) p. 46. The formula C^H^N 18 © 40 , or C 64 H 42 N 9 0 20 , gives, when reduced to 100 parts, C 64 50-07 H 42 . ... 6-35 N 9 19-32 O 20 24-26 Compare this with the composition of gelatine, as given in Note (27) NOTE (37,) p. 49. COMPOSITION OF DITHOFELLIC ACID.a Ettling and Will.* Wcehler.* c40h!»O8 Carbon . . 7H9 7?80 70-83 7083 Hydrogen . . 10>85 10-78 10-95 10-60 10-48 Oxygen . . 1796 1842 1882 18-57 1869 a Annalen der Chem. und Pharm., XXXIX., 242, and XLI., 154. NOTE (38,) p. 56. COMPOSITION OF SOLANINE FROM THE BUDS OF GERMINATING POTATOES, fit BJanchet. Carbon 62-11 Hydrogen 8-92 Nitrogen 1-64 Oxygen 27-33 a Ann. der Pharm., VII., 150. NOTE (39,) p. 56. COMPOSITION OF PICROTOXINE. (I Francis.* Carbon 60-26 Hydrogen • 5-70 Nitrogen 1-30 Oxygen 32-74 a In another analysis, M. Francis obtained 0-75 per cent, of nitrogen. The picrotoxine employed for these analyses was partly obtained from the manufactory of M. Merck, in Darmstadt, and was partly prepared by M. Francis himself; it was perfectly white, and beautifully crystallized. Regnault, as is well known, found no nitrogen in this compound. NOTE (40,) p. 56. COMPOSITION OF Q.UININE. Liebig.* Calculated C20H12NO2. Carbon 75-76 74-39 Hydrogen .... 7-52 7-25 Nitrogen 8-11 8-52 Oxygen .... 8-62 9-64 NOTE (41,) p. 156. COMPOSITION OF MORPHIA, (t Calculated Liebig.* Regnault. . C35H20NO6 Carbon . . . 72-340 72-41 72-28 Hydrogen . . 6-366 6-86 6-84 6-74 Nitrogen. . . 4-995 5-01 5-01 4-80 Oxygen . . 16299 15-26 1574 16-18 o Ann. der Pharm., XXVI., 23. APPENDIX.—ANALYTICAL EVIDENCE. 101 NOTE (42,) p. 156. COMPOSITION OF CAFFEINE, THEINE, GUARANINE, THEOBROMINE, AND ASPARAGINE. Caffeine, a Theine. 6 Ouaranine. c Calculated Pfaffand Liebig.* Jobst. Martius. C8H5N202 Carbon . . 49-77 50-101 49-679 49-798 Hydrogen . 5-33 5214 5-139 5082 Nitrogen . . 28-78 29-009 29-180 28-832 Oxygen . . 16-12 15-676 16-002 16-288 a Ann. der Pharm., I., 17. 6 Ann. der Pharm., XXV., 63. c Ann. der Pharm., XXVI., 95. Guaranine is the name given to the crystallized principle of the guarana officinalis, till jt was shown to be identical with caffeine and theine, as the above analyses demonstrate. COMPOSITION OF THEOBROMINE, d Calculated Woskreseusky. C9H5N302 Carbon ... '47-21 46W 46-71 46-43 Hydrogen . . 4-53 4-61 4-52 4-20 Nitrogen . . . 35-38 35 38 35 38 35 85 Oxygen . . 12-88 1304 13-39 13-51 a Ann. der Chem. und Pharm., xli., 125. COMPOSITION OF ASPARAGINE. tt Liebig. Calculated C8H8N206 + 2HO Carbon . . . 32-351 32-35 Hydrogen. . . 6844 6-60 Nitrogen , . . 18734 18-73 Oxygen . . . 42021 42-32 a Ann. der Pharm., VII., 146. ON THE CONVERSION OF BENZOIC ACID INTO HIPPURIC ACID.* BY WILHELM KELLER. (From the Annalen der Chemie und Pharmacie.) So early as in the edition of Berzelius* "Lehrbuch der Chemie," published in 1831, Professor Wohler had expressed the opinion, that benzoic acid, during digestion, was probably converted into hippuric acid. This opinion was founded on an experiment which he had made on the passage of benzoic acid into the urine. He found in the urine of a dog which had eaten half a drachm of benzoic acid with his food, an acid crystallizing in needle-shaped prisms, which had the general properties of benzoic acid, and which he then took for benzoic acid. (Tiedemann's Zeitschrift fur Physiologie, i. 142.) These crystals were obviously hippuric acid, as plainly appears from the statements, that they had the aspect of nitre, and, when sublimed, left a residue of carbon. But at that time hippuric acid was not yet discovered ; and it is well known that, till 1829, when these acids were first distinguished from each other by Liebig, it was uniformly confounded with benzoic acid. The recently published statement of A. Ure, that he actually found hippuric acid in the urine of a patient who had taken benzoic acid, recalled this relation, so remarkable in a physiological point of view, and induced me to undertake the following experiments, which, at the suggestion of Professor Wohler, I made on myself. The supposed conversion of benzoic acid into hippuric acid has, by these experiments, been unequivocally established. I took, in the evening before bed-time, about thirty-two grains of pure benzoic acid in syrup. During the night I perspired strongly, which was probably an effect of the acid, as in general I am with great difficulty made to transpire profusely. 1 could perceive no other effect, even when, next day, I took the same dose three times j indeed, even the perspiration did not again occur. The urine passed in the morning had an uncommonly strong acid reaction, it had been evaporated, and had stood for twelve hours. It deposited only the usual sediment of earthy salts. 'But when it was mixed with muriatic acid, and allowed to stand, * To the evidence produced by A. Ure, of the conversion of benzoic acid into hippuric acid in the human body, M. Keller has added some very decisive proofs, which I append to this work on account of their physiological importance. The experiments of M. Keller were made in the laboratory of Professor Wohler, at Gottingen; and they place beyond all doubt the fact that a non-azotized substance taken in the food can take a share, by means of its elements, in the act of transformation of the animal tissues, and in the formation ot a secretion. This fact throws a clear light on the mode of action of the greater number of remedies ; and if the influence of caffeine on the formation of urea or uric acid should admit of being demonstrated in a similar way, we shall then possess the key to the action of quinine and of the other vegetable alkalies. —J. L. 102 ANIMAL CHEMISTRY. there were formed in it long prismatic, brownish crystals, in great quantity, which, eve a in this state, could not be taken for benzoic acid. Another portion, evaporated to the consistence of syrup, formed, when mixed with muriatic acid, a magma of crystalline scales. The crystalline mass was pressed, dissolved in hot water, treated with animal charcoal, and recrystallized. By this means the acid was obtained in colourless prisms, an inch in length. Their crystals were pure hippuric acid. When heated, they melted easily; and when exposed to a still stronger heat, the mass was carbonized, with a smell of oil of bitter almonds, while benzoic acid sublimed. To remove all doubts, I determined the proportion of carbon in the crystals, which I found to be 60*4 per cent. Crystallized hippuric acid, according to the formula C 18 H 8 N0 5 + HO, contains 60-67 per cent, of carbon; crystallized benzoic acid, on the other hand, contains 69 - 10 per cent, of carbon. As long as I continued to take benzoic acid, I was able easily to obtain hippuric acid in large quantity from the urine; and since the benzoic acid seems so devoid of any injurious effect on the health, it would be easy in this way to supply one's self with large quantities of hippuric acid. It would only be necessary to engage a person to continue for some weeks this new species of manufacture. It was of importance to examine the urine which contained hippuric acid, in reference to the two normal chief constituents, urea and uric acid. Both were contained in it, and apparently in the same proportion as in the normal urine. The inspissated urine, after the hippuric acid had been separated by muriatic acid, yielded, on the addition of nitric acid, a large quantity of nitrate of urea. It had previously deposited a powder, the solution of which in nitric acid gave, when evaporated to dryness, the well-known purple colour characteristic of uric acid. This observation is opposed to the statement of Ure; and he is certainly too hasty in recommending benzoic acid as a remedy for the gouty and calculous concretions of uric acid. He seems to suppose that the uric acid has been employed in the conversion of benzoic acid into hippuric acid; but as his observations were made on a gouty patient, it may be supposed that the urine, even without the internal use of benzoic acid, would have been found to contain no uric acid. Finally, it is clear that the hippuric acid existed in the urine in combination with a base, because it only separated after the addition of an acid. THE END. INDEX. A. Acid, Acetic. Composition; and relation to that of aldehyde, 80, 81. Acid, Benzoic. Composition, and relation to that of oil of bitter almonds, 80,81. Converted into hippuric acid in the human body, 48, 101. Acid, Carbonic. Is the form in which the in- spired oxygen and the carbon of the food are given out, 14. Its formation in the body the chief source of animal heat, 15—16. Occurs combined with potash and soda, in the serum of the blood, 21. Formed by the action of oxygen on the products of the metamorphosis of the tissues, 26. Its formation may also be connected with the production of fat from starch, 32—34. Generated by putrefaction of food in the stomach of animals, 39. Also by the fermentation of bad wine in man, when it causes death by penetrating into the lungs, 39. Escapes through both skin and lungs, 39. Produced, along with urea, by the oxidation of uric acid, 45. Produced with several other compounds, by the oxidation of blood, 45. May be formed, along with choleic acid, from hippuric acid, starch and oxygen, 49. Also, along with choleic acid, urea, and ammonia, by the action of water and oxygen on starch and proteine, 49. Produced, along with fat and urea, from proteine, by the action of water and oxygen, in the absence of soda, 49. Combines with the compound of iron present in venous blood, and is given off when oxygen is absorbed, 78. Is absorbed by the serum of blood in all states, 78. Acid, Cerebric. Its composition, 57. Tts properties, 58. Acid, Choleic. Represents the organic portion of the bile, 44. Its formula, 44. Its trans- formations, 42. Half its formula, added to that of urate of ammonia, is equal to the formula of blood -f- a little oxygen and water, 44. Produced in the oxidation of blood, 45. Views which may be taken of its composition, 47. May be formed by the action of oxygen and water on proteine and starch, 48. Products of its oxidation, 49. Various ways in which it may be supposed to be formed in the body, 51. Its composition, 96. Cannot be said to exist ready formed in the bile, 97. Acid, Cholic. Its composition, 98. Derived from choleic acid, 44. Possible relation to choleic acid, 47. Acid, Choloidic. Its composition, 96. Derived from choleic acid, 44. Possible relation to choleic acid, 47. Possible relation to starch, 51. Possible relation to proteine, 46. Acid, Cyanic. Its formula, 81. Acid, Cyanuric. Its formula, 81. Acid, Hippuric. Its composition, 98. Appears in the urine of stall-fed animals, 31. Is de- stroyed by exercise, 31,45. Is probably formed in the oxidation of blood, 45. Is found in the human urine after benzoic acid has been ad- ministered, 48, 101. May be derived from proteine when acted on by oxygen and uric acid, 48. With starch and oxygen, it may produce choleic and carbonic acids, 48. May be derived from the oxidation of choleic acid, 49. Acid, Hydrocyanic or Prussic. Its poisonous action explained, 80. Acid, Lithofellic. Its composition, 100. Probably derived from the oxidation of choleic acid: is the chief constituent of bezoar stones, 49. Acid, Laetic. Its composition, 93. Its origin, 38. Does not exist in the healthy gastric juice, 38. Acid, Margaric. Exists in bile, 97. Acid, Muriatic. Exists in the free state in the gastric juice, 37, 38. Is derived from common salt, 38, 52. Acid, Oxaluric. Analysis of, 99. Acid, Parabanic. Analysis of, 99. Acid, Phosphoric. Exists in the urine of the carnivora in considerable quantity, 30, 52. Its proportion very small in that of the graminivora, 31. Derived from the phosphorus of the tissues, 30. It is retained in the body to form bones and nervous matter, 31. Acid, Sulphuric. Exists in the urine of the carnivora, 30, 52. Derived from the sulphur of the tissues, 30. Acid, Uric. Its composition, 98. Products of its oxidation, alloxan, carbonic acid, oxalic acid, urea, &c, 45. Is probably derived, along with choleic acid, by the action of oxygen and water on blood or muscle, 44. Disappears almost entirely in the system of man and of the higher animals, 24, 41. Appears as calculus, when there is a deficiency of oxygen, 44. Never occurs in phthisical cases, 45. Yields mulberry calculus when the quantity of oxygen is somewhat increased, but only urea and carbonic acid with a full supply of oxygen, 45. Uric acid calculus promoted by the use of fat and of certain wines, 45. Unknown on the Rhine, 45. Uric acid and urea, how related to allantoine, 46; to gelatine, 46. Forms the greater part of the urine of serpents, 24. Yields, with the elements of proteine and oxygen, hippuric acid and urea, 48. How related to taurine, 49. Calculi of it never occur in wild carnivora, but often in men who use little animal food, 47. Affinity, Chemical. Is the ultimate cause of the vital phenomena, 13. Is active only in the case of contact, and depends much on the order in which the particles are arranged, 62. Its equilibrium renders a compound liable to transformations, 63. In producing the vital phenomena, it is modified by other forces, 63. It is not alone the vital force or vitality, but is exerted in subordination to that force, 70. Air. Introduced into the stomach during digestion 103 104 INDEX with the saliva, 38. Effects of its temperature and density, dryness, &c, in respiration, 14,15. Albumen. Animal and vegetable albumen identical, 22, 23. Their composition, 87, 93. Vegetable albumen, how obtained, 22. Is a com* pound of proteine, and in organic composition identical with fibrine and caseine, 36,37. Exists in the yolk as well as the white of eggs, 37. Also in the serum of the blood, 21. Is the true starting point of all the animal tissues, 37. Alcohol. Is hurtful to carnivorous savages, 56. Its mode of action: checks the change of matter, 72. In cold climates serves as an element of respiration, 16. Aldehyde. Its composition; how related to that of acetic acid, 80, 81. Alkalies. Mineral alkalies essential both to vegetable and animal life, 52. Vegetable alkalies all contain nitrogen, all act on the nervous system, and are all poisonous in a moderate dose, 56, 57. Theory of their action: they take a share in the transformation or production of nervous matter, for which they are«adapted by their composition, 57—59. Action of caustic alkalies on bile, or choleic acid, 44. Allantoine. Is found in the urine of the foetal calf. How derived from proteine. How related to uric acid and urea, 46. How related to choleic acid, 47. Its composition, 98. Allen and Pepys. Their calculation of the amount of inspired oxygen, 82. Alloxan. Formed by the oxidation of uric acid, 45. Converted by oxidation into oxalic acid and urea, oxaluric and parabanic acids, or carbonic acid and urea, 45. How related to tau- rine, 50. Seems to act as a diuretic. Recommended for experiment in hepatic diseases, 45. (iiote.) Almonds, Bitter. Oil of. Its composition; how related to benzoic acid, 81. Ammonia. Combined with uric acid it forms the urine of serpents, birds, &c, 24. Its relation to choleic, choloidic, and cholic acids, 44. Is one of the products which may be formed by the oxidation of blood, 45; or of proteine, 48. Its relation to uric acid, urea, and taurine, 49. To allantoine and taurine, 49. To alloxan and taurine, 49. To choleic and choloidic acid and taurine, 50. To urea, water, and carbonic acid, 51. Is found in combination with acids in the urine of the carnivora, 52. Analysis. Of dry blood, 82, 96. Of dried flesh, 96. Of faeces, 83. Of black bread, 83. Of potatoes, 83. Of peas, 83. Of beans, 83. Of lentils, 83. Of fresh meat, 83. Of moist bread, 83. Of moist potatoes, 83. Of the fibrine and albumen of blood, 87, 94. Of vegetable fibrine and albumen, vegetable caseine and gluten, 88. Of animal caseine, 88. Of starch, 88. Of grape or starch sugar, 88. Of sugar of milk, 89. Of gum, 89. Of oats, 89. Of hay, 89. Of fat, 90. Of cane-sugar, 90. Of cholesterine, 90. Of wax, 92. Of cyanic acid, cyanuric acid, and cyamelide, 92. Of aldehyde, metaldehyde, and elaldehyde, 92. Of proteine, 93. Of albumen from the yolk and white of egg, 93. Of lactic acid, 93. Of gas from the stomach of cows after eating to excess, 93. Of gas from stomach and intestines of executed criminals, 93. Of gelatinous tissues, 94. Of tissues containing chondrine, 95. Of arterial membrane, 95. Of horny tissues, 95. Of the lining membrane of the egg, 95. Of feathers, 95. Of the pigmentum nigrum, 95. Of choleic acid, 96. Of taurine, 96. Of choloidic acid, 96. Of cholic acid, 98. Of uric acid, 98. Of alloxan, 98. Of urea, 98. Of hippuric acid, 98. Of allantoine, 98. Of xanthic oxide, 99. Of cystic oxide, 99. Of oxalic acid, 99. Of oxaluric acid, 99. Of parabanic acid, 99. Of roasted flesh, 100. Of )$iofellic acid, 100. Of solanine, 100. Of picrotoxine, 100. Of quinine, 100. Of morphia, 101. Of caffeine, theine, or guaranine, 101. Of theobromine, 101. Of asparagine, 101. Animal Heat. Derived from the combination of oxygen with the carbon and hydrogen of the metamorphosed tissues, which proceed ultimately from the food, 15. Is highest in those animals whose respiration is most active, 15. Is the same in man in all climates, 15, 16. Is kept up by the food in proportion to amount of external cooling, 16. Is not produced either by any direct influence of the nerves, or by muscular contractions, 18, 19. Its amount in man, 19. Chemical action the sole source of it, 20. The formation of fat from starch or sugar must produce heat, 34. The elements of the bile, by combining with oxygen, serve chiefly to produce it, 26. Animal Life. Distinguished from vegetable life by the absorption of oxygen, and the production of carbonic acid, 11. Must not be con- founded with consciousness, 12. Conditions necessary to animal life, 13, 14. Depends on an equilibrium between waste and supply, 72, 74, 75. Antiseptics. They act by putting a stop to fermentation, putrefaction, or other forms of metamorphosis, 54. Their action on wounds and ulcers, 41. Arteries. Composition of their tunica media, 95. How derived from proteine, 42. Arterial Blood. Conveys oxygen to every part of the body, 26, 77. Contains a compound of iron, most probably peroxide, 77. Yields oxygen in passing through the capillaries, 26,79. Contains carbonic acid dissolved or combined with soda, 79. Asparagine. Its composition, 101. Its relation to taurine and bile, 56. Theory of its action on the bile, 57. Assimilation. In animals it is independent of external influences, 11. Depends on the presence in the blood of compounds of proteine, such as fibrine, albumen, or caseine, 21. Is more energetic in the young than in the adult animal, 27. Is also more energetic in the herbivora than, in the carnivora, 31. Atmosphere. See Air. Azotized Products. Of vegetable life, 55—57. Of the metamorphosis of tissues. Necessary for the formation of bile in the herbivora, 51. In man, 53. May be replaced by azotized vegetable compounds, 54. Theory of this, 56— 57. Of the transformation of the bile, or of choleic acid; how related to the constituents of urine, 50. B. Beans. Composition of, 83. Beer. Forms part of the diet of soldiers in Ger« many, 83, 85. INDEX 105 Bees. Their power of forming wax from honey, 90—92. Benzoic Acid. See Acid, Benzoic. Berthollet His analysis of oxalic acid, 99. Berzelius. His analysis of potato starch, 88; of sugar of milk, 89; of gum, 89; of cane sugar, 90. Bezoar stones. See Acid, Lithofellic Blanchet. His analysis of solanine, 100. Bile. In the carnivora is a product of the metamorphosis of the tissues, along with urate of ammonia, 44. May be represented by choleate of soda, with which, however, it is not identical, 97. Products of its transformation, 44, 97. Remarks on these, 96—97. Origin of bile, 26, 46. Starch, &c, contribute to its formation in the herbivora, 47, 48, 51, 53. Soda essential to it, 49, 52. Relation of bile to urine, 50. To starch, 51. To fibrine, 44. To caffeine, &c, asparagine, and theobromine, 57. For the acid substances derived from bile, choleic, choloidic, and cholic acids, see Acid, Choleic, &c. Yields taurine, 44. Contains cholesterine, 32, 97. Also stearic and margaric acids, 97. Its function: to support respiration and produce animal heat by presenting carbon and hydrogen in a very soluble form to the oxygen of the arterial blood, 26,27. Amount secreted by the dog, the horse, and man, 27. It returns entirely into the circulation, and disappears completely, 26, 27. Blood. The fluid from which every part of the body is formed, 13. Its chief constituents, 21. How formed from vegetable food, 22. Can only be formed from compounds of proteine, 23. Is therefore entirely derived from vegetable products in the herbivora, and indirectly also by the carnivora, which feed on the flesh of the former, 23. Its composition identical with that of flesh, 44. Analysis of both, 96. The secretions contain all the elements of the blood, 43. Its relation to bile and urine, 44. Products of the oxidation of blood, 45. Excess of azotized food produces fulness of blood and disease, 47. Soda is present in the blood, 52. Important properties of the blood, 54—55. Venous blood contains iron, probably as protoxide ; arterial blood, probably as peroxide, 79. Theory of the poisonous action of sulphuretted hydrogen and prussic acid: they decompose the compound of iron in the blood, 79. The blood, in analogous morbid states, ought to be chemically examined, 80. Blood-letting. Theory of its mode of action, 78. It may produce opposite effects in different cases, 77. Boeckmann. His analysis of black bread, 83; of potatoes, 83; of dry beef, 96; of dry blood, 96; of roasted flesh, 100. Bones. Phosphoric acid of the food retained to assist in forming them, 31. Gelatine of bones digested by dogs, 35. See, further, Gelatine. Cause of brittleness in bones, 36. Boussingault. His analysis of potatoes, 83. His comparison of the food and excretions in the horse and cow, Table, 86. His analysis of gluten, 87; of vegetable albumen, 87; of vegetable caseine, 88; of oats, 89; of hay, 89. Braconnot. On the presence of lactic acid in gastric juice, 38; of iron in the gastric juice of the dog, 38. Brain. See Acid, Cerebric, and Nervous Matter. 14 Bread. Analysis of, 83. Brund. His analysis of sugar of milk, 89. Buckwheat. Analysis of starch from, 88. Burdach. His statement of the amount of bile secreted by animals, 27. Butter. Forms a part of the food of soldiers in Germany, 83, 84. Buzzard. Its excrements consist of urate of am- monia, 24. C. Caffeine. Identical with theine, 56. Its relation to taurine and bile, 56. Theory of its mode of action, 57. Its composition, 101. Cane Sugar. Its composition, 90. Carbon. Is accumulated in the bile, 21. Is given off as carbonic acid, 14. Excess of carbon causes hepatic diseases, 17. By combining with oxygen, it yields the greater part of the animal heat. See Animal Heat, Bile, and Acid, Carbonic. Amount of carbon oxidized daily in the body of a man, 14. Calculations on which this statement is founded, 82—85. Amount consumed by the horse and cow, 14. Different proportions of carbon in different kinds of food, 15. Carbon of flesh compared with that of starch, showing the advantage of a mixed diet, 30. Calculation on which this statement is founded, 89. Amount of carbon in dry blood calculated, 82. Amount in the food of prisoners calculated, 87. Carbonic Acid. See Acid, Carbonic. Carbonates. They occur in the blood, 21. Calculus, Mulberry. Derived from the imperfect oxidation of uric acid, 45. Uric acid calculus is formed in consequence of deficiency of inspired oxygen, or excess of carbon in the food, 45. See Acid, Uric. Bezoar stones composed of lithofellic acid, 49. Carnivora. Their nutrition the most simple, 22. It is ultimately derived from vegetables, 23. Their young, like graminivora, require nonazotized compounds in their food, 23. Their bile is formed from the metamorphosis of their tissues, 25, 26. The process of assimilation in adult and young carnivora compared, 27. Their urine, 30. The assimilative process in adult carnivora less energetic than in graminivora, 31. They are destitute of fat, 31. They swallow less air with their food than graminivora, 40. Concretions of uric acid are never found in them, 47. Both soda and ammonia found in their urine, 52. Caseine. One of the azotized nutritious products of vegetable life, 22. Abundant in leguminous plants, 22. Identical in organic composition with fibrine and albumen, 22, 23. Animal caseine found in milk and cheese; identical with vegetable caseine, 23. Furnishes blood to the young animal, 24. Is one of the plastic elements of nutrition, 35. Yields proteine, 37. Its relation to proteine, 42. It contains sulphur, 42. Potash essential to its production, 52. Contains more of the earth of bones than blood docs, 24. Its analysis, 88. Cerebric Acid. See Acid, Cerebric. Change of Matter. See Metamorphosis of Tissues. Chemical Attraction. See Affinity. Chevreul. His researches on fat, 32. His ana- lysis of fat, 90; of cholesterine, 90. Chloride of Sodium* See Common Salt Choleic Acid. See Acid, Choleic. 106 INDEX Cholesterine. See Bile. Cholic Acid. See Acid, Cholic. Choloidic Acid. See Acid, Choloidic. Chondrine. Its relation to proteine, 42. Analysis of tissues containing it, 95. Chronic Diseases. The action of inspired oxygen is the cause of death in them, 17, 18. Chyle. When it has reached the thoracic duct, it is alkaline, and contains albumen coagulable by heat, 47. Chyme. It is formed independently of the vital force, by a chemical transformation, 37. The substance which causes this transformation is derived from the living membrane of the stomach, 37. Chyme is acid, 47. Clothing. Warm clothing is a substitute for food to a certain extent, 16. Want of clothing accelerates the rate of cooling, and the respirations, and thus increases the appetite, 16. Cold. Increases the appetite by accelerating the respiration, 16. Is most judiciously employed as a remedy in cerebral inflammation, 76. Concretions. See Calculus, and Acid, Uric; also Acid, Lithofellic. Constituents, Azotized. Of blood: see Fibrine and Albumen. Of vegetables: See Fibrine, Vegetable; Albumen, Vegetable; Caseine, Vegetable; Alkalies, Vegetable; and Caffeine. Of bile: see Acid, Choleic, Cholic, and Cho- loidic. Of urine: see Acid, Uric; Urea, and Allantoine. Cooling. See Cold and Clothing. Couerbe. His analysis of cholesterine, 90. Cow. Amount of carbon expired by the, 14. Comparison of the food with the excretions of the cow, 86. Crum. His analysis of cane sugar, 90. Cultivation. Is the economy of force, 30. Cyamelide. Its formula, 81. Cyanic Acid. See Acid, Cyanic. Cyanide of Iron. Its remarkable properties, 78. Cyanuric Acid. See Acid, Cyanuric. D. Davy. Oxygen consumed by an adult man, 82. Death. Cause of, in chronic diseases, 17, 18. Caused in old people by a slight depression of temperature, 75. Definition of it, 74. Demargay. His analysis of choleic acid, choloidic acid, and taurine, 96. Remarks on his Re- searches on Bile, 97. Denis. His experiments on the conversion of fibrine into albumen, 21. Despretz. His calculation of the heat developed in the combustion of carbon, 19. Diabetes Mellitus. The sugar found in the urine in this disease is grape sugar, and is derived from the starch of the food, 35. Diastase. Analogy between its solvent action on starch, and that of the gastric juice on coagulated albumen, 38. Diffusion of Gases. Explains the fact that nitrogen is given out through the skin of animals, 40; and the poisonous action of feather-white wine, 39. Digestion. Is effected without the aid of the vital force, by a metamorphosis derived from the transformation of a substance proceeding from the lining membrane of the stomach, 37. The oxygen introduced with the saliva assists in the process, 38. Lactic acid has no share in it, 38. Disease. Theory of, 74 et seq. Cause of death in chronic disease, 17. Disease of liver caused by excess of carbon or deficiency of oxygen, 16. Prevails in hot weather, 17. Dog. Amount of bile secreted by, 27. Digests the gelatine of bones, 35. His excrements contain only bone earth, 36. Concretion of urate of ammonia said to have been found by Lassaigne in a dog, doubtful, 47 (note.) Dumas. His analysis of choleic acid, 96; of choloidic acid, 96; of taurine, ib.; of cholic acid, 97; of hippuric acid, 98. E. Eggs. Albumen of the white and of the yolk identical, 37. Analysis of both, 93; of lining membrane, 95. The fat of the yolk may contribute to the formation of nervous matter, 37. This fat contains iron, 37. Elaldehyde. See Aldehyde. Elements. Of nutrition, 35. Of respiration, 35. Empyreumatics. They check transformations, 54. Their action on ulcers, 41. Equilibrium. Between waste and supply of matter is the abstract state of health, 74, 78. Transformations occur in compounds in which the chemical forces are in unstable equilibrium, 37. Ettling. His analysis of wax, 92. Ettling and Will, their analysis of lithofellic acid, 100. Excrements. Contain little or no bile in man and in the herbivora, none at all in the dog and other carnivora, 27. Those of the dog are phosphate of lime, 35. Those of serpents are urate of ammonia, 24. Those of birds also contain that salt, 24. Those of the horse and cow compared with their food, 86. Excretions. Contain, with the secretions, the elements of the blood or of the tissues, 43, 44. Those of the horse and cow compared with their food, 86. Bile is not an excretion, 26. F. Faeces.. Analysis of, 83. Fat. Theory of its production from starch, when oxygen is deficient, 32 et seq. ; from other substances, 32. The formation of fat supplies a new source of oxygen, 33; and produces heat, 33 et seq. Maximum of fat, how obtained, 34. Carnivora have no fat, 31. Fat in stall-fed animals, 33. Occurs in some diseases in the blood, 35. Fat in the women of the East, 36. Composition compared with that of sugar, 32. Analysis of fat, 90. Disappears in starvation, 17. Is an element of respiration, 35. Fattening of Animals. See Fat. Featherwhite Wine. Its poisonous action, 39. Febrile Paroxyism. Definition of, 75. Fehling. His analysis of metaldehyde and elaldehyde, 92. Fermentation. May be produced by any azotized matter in a state of decomposition, 40. Is arrested by empyreumatics, 40. • Is analogous to digestion, 40. Fever. Theory and definition of, 75. Fibre. Muscular. See Flesh. Fibrine. Is an element of nutrition, 35. Animal and vegetable fibrine are identical, 22. Is a compound of proteine, 36. Its relation to proteine, 42. Convertible into albumen, 21. Is derived from albumen during incubation, 37. Its analysis, 87, 94. Vegetable fibrine, how obtained, 22. INDEX 107 Pishes. Yield phosphuretted hydrogen, 59 (note.) Flesh. Consists chiefly of fibrine, but, from the mixture of fat and membrane, has the same formula as blood, 44. Analysis of flesh, 96,100. Amount of carbon in flesh compared with that of starch, 30, 86. - Food. Must contain both elements of nutrition and elements of respiration, 35. Nutritious food, strictly speaking, is that alone which is capable of forming blood, 21. Whether derived from animals or from vegetables, nutritious food contains proteine, 22, 37 et seq. Changes which the food undergoes in of the carnivora, 24 et seq. The f