CHAPTER XIX.

THE ELIMINATION OF WASTE SUBSTANCES.

The expenditures of the human body, or the waste products which

arise from the activity of the master tissues, are thrown off by

the excretory tissues, as the lungs, the skin, the kidneys, and the

terminal part of the intestines.

The lungs are hollow organs, and we may consider them as really two

bags containing air, each of which communicates by a separate orifice

with a common air tube, through the upper part of which, the larynx,

they freely communicate with the external atmosphere. The orifice of

the larynx is guarded by muscles, and can be opened or closed at will.

Each lung is partially subdivided into separate portions called

lobes. The right lung has three lobes, and the left lung has two. Each

of these lobes, again, is composed of a large number of minute parts,

called lobules. Each pulmonary lobule may be considered a lung in

miniature, consisting as it does of a branch of a bronchial tube,

air-cells, blood-vessels, nerves, and lymphatics, with a sparing

amount of areolar tissue.

The terminal portion of each lobule is composed of a group of

pouches or air-cells, which communicate with the intercellular air

passages. These cells are of various forms, according to the mutual

pressure to which they are subject. Their cell walls are nearly in

contact, and they vary from 1/50 to 1/90 of an inch in diameter.

Outside the cells a network of pulmonary capillaries is spread out

so densely that the interspaces or meshes are even narrower than the

vessels, which are on an average 1/3000 of an inch in diameter.

Between the atmospheric air in the cells and the blood in the

vessels nothing intervenes but the thin membrane of the cells and the

capillaries, and the delicate epithelium lining the former. And the

exposure of the blood to the air is the more complete because the folds

of membrane between contiguous cells, and often the spaces between

the walls of the same, contain only a single layer of capillaries,

both sides of which are thus at once exposed to the air.

The enlargement of the capacity of the chest in inspiration is a

muscular act; the muscles concerned in producing the effect being

chiefly the diaphragm, the external intercostal muscles, etc.

From the enlargement produced in inspiration, the chest and lungs

return in ordinary tranquil expiration by their elasticity; the

force employed by the inspiratory muscles in distending the chest and

overcoming the elastic resistance of the lungs and chest wall being

returned as an expiratory effort when the muscles are relaxed.

The acts of expansion and of contraction of the chest take up, under

ordinary circumstances, a nearly equal time, and can scarcely be said

to be separated from each other by an intervening pause. The quantity

of air that is changed in the lungs in each act of ordinary tranquil

breathing is variable, but probably 30 to 35 cubic inches are a fair

average in the case of healthy young and middle-aged men. The total

quantity of air which passes into and out of the lungs of an adult,

at rest, in 24 hours, has been estimated to be about 686,000 cubic

inches. This quantity is largely increased by exertion; and it has

been computed that the average amount for a hard-working laborer in

the same time is 1,568,390.

Breathing air is the quantity of air which is habitually and almost

uniformly changed in each act of breathing.

Complemental air is the quantity of air over and above this which a

man can draw into the lungs in the deepest inspiration.

After ordinary expiration, such as that which expels the breathing

air, a certain quantity of air remains in the lungs which may be

expelled by a forcible and deeper expiration; this is termed reserve

air. But even after the most violent expiratory effort, the lungs are

not completely emptied; a certain quantity of air remains in them,

over which there is no voluntary control, which may be called residual

air. Its amount depends, in great measure, on the absolute size of the

chest, and has been variously estimated at from 40 to 200 cubic inches.

Power of Inspiratory Power of Expiratory

Muscles. Muscles.

1.5 inches. weak 2.0 inches.

2.0   ,,    ordinary 2.5   ,,

2.5   ,,    strong 3.5   ,,

3.5   ,,    very strong 4.5   ,,

4.5   ,,    remarkable 5.8   ,,

5.5   ,,    very remarkable 7.0   ,,

6.0   ,,    extraordinary 8.5   ,,

7.0   ,,    very extraordinary 10.0   ,,

The blood as it moves through the respiratory organs is exposed

to the air that alternately moves into and out of the air-cells

and minute bronchial tubes. The blood is propelled from the right

ventricle through the pulmonary capillaries in steady streams, and

slowly enough to permit every minute portion of it to be for a few

seconds exposed to the air, with only the thin walls of the capillary

vessels and air-cells intervening.

The atmosphere we breathe has in every situation in which it has been

examined in its natural state a nearly uniform composition. It is a

mixture of oxygen and nitrogen, carbonic acid, and watery vapor, with

traces of other gases, as ammonia, sulphuretta, hydrogen, etc. Of

every 100 volumes of pure atmospheric air, 79 volumes consist of

nitrogen and 21 of oxygen, about. The proportion of carbonic acid

is extremely small: 10,000 volumes of atmospheric air contains only

about 4 or 5 of carbonic acid. The average quantity of watery vapor

in the atmosphere in this country is about 1.40 per cent.

The changes produced by respiration on the atmosphere are that:

1. It is warmed; 2. Its carbonic acid is increased; 3. Its oxygen is

diminished; 4. Its watery vapor is increased; 5. A minute amount of

organic matter and of free ammonia is added to it.

1. The expired air is hotter than the inspired air. The temperature

varies from 97° to 99 1/2°.

2. Carbonic acid in respired air is always increased; but the

quantity exhaled in a given time is subject to change from various

circumstances. From every volume of air inspired about 4 1/2 per cent

of oxygen is abstracted; while rather a smaller quantity of carbonic

acid is added in its place. Under ordinary circumstances, the quantity

of carbonic acid exhaled into the air breathed by a healthy adult

man amounts to 1,346 inches, or about 636 grains, per hour. It is

estimated that the weight of carbon excreted from the lungs is about

173 grains per hour, or rather more than 8 ounces in 24 hours.

Of course the influence of age, sex, respiratory movements,

external temperature, season of the year, purity of the respired air,

hygrometric state of the atmosphere, period of day, food and drink,

exercise and sleep, have to be taken in consideration.

The oxygen of respired air is always less than in the same air before

respiration, and its diminution is generally proportionate to the

increase of the carbonic acid. It has been shown that for every volume

of carbonic acid exhaled into the air 1.17421 volumes of oxygen are

absorbed from it; and that when the average quantity of carbonic acid,

i.e., 1,346 cubic inches, or 636 grains, is exhaled in the hour, the

quantity of oxygen absorbed in the same time is 1,584 cubic inches,

or 542 grains.

The nitrogen in the atmosphere, in relation to the respiratory process

is supposed to serve only mechanically, by diluting the oxygen,

and moderating the action upon the system.

The most obvious change which the blood undergoes in its passage

through the lungs is that of color, the dark venous blood being

exchanged for the bright scarlet arterial blood. It gains oxygen,

loses carbonic acid, becomes 1° to 2° F. warmer; it coagulates sooner

and more firmly, and contains more fibrine.

The venous blood as it issues from the right ventricle is loaded with

carbonic acid. The oxygen present is insufficient to the whole of the

hæmoglobin of the red corpuscles; much reduced hæmoglobin is present,

hence the purple color of venous blood. As the blood-vessels pass

through the capillaries of the lungs, this reduced hæmoglobin takes

from the pulmonary air its complement of oxygen, all or nearly all

the hæmoglobin of the red corpuscles becomes oxy-hæmoglobin, and the

purple color forthwith shifts into scarlet. The hæmoglobin of arterial

blood is saturated or nearly saturated with oxygen. Passing from

the left ventricle to the capillaries, some of the oxy-hæmoglobin

gives up its oxygen to the tissues, becomes reduced hæmoglobin,

and the blood in consequence becomes once more venous, with a

purple hue. Thus the red corpuscles by virtue of their hæmoglobin

are emphatically oxygen-carriers. Undergoing no intrinsic change in

itself, the hæmoglobin combines in the lungs with oxygen, which it

carries to the tissues; these, more greedy of the oxygen than itself,

rob it of its charge, and the reduced hæmoglobin hurries back to the

lung in venous blood for another portion. Hæmoglobin combines loosely

with carbonic oxide just as it does with oxygen, but the affinity

with the former is greater than with the latter. While carbonic oxide

readily turns out oxygen, oxygen cannot so readily turn out carbonic

acid. This property of carbonic oxide explains its poisonous nature.

Respiratory changes in the tissues. Arterial blood passing through the

several tissues, becomes once more venous. A considerable quantity

of the oxy-hæmoglobin becomes reduced, and a quantity of carbonic

acid passes from the tissue into the blood. The blood which comes

from a contracting muscle, is not only richer in carbonic acid,

but also, though not to a corresponding amount, poorer in oxygen,

than the blood which flows from a muscle at rest.

A muscle is always producing carbonic acid, and when it contracts there

is a sudden and extensive increase of the normal production. Oxygen

is necessary for the life of the muscle. When venous blood instead

of arterial blood is sent through the blood-vessel of a muscle,

the irritability speedily disappears, and unless fresh oxygen be

administered the muscle soon dies.

Our knowledge of the respiratory changes in muscle is more complete

than in the case of any other tissue; but we have no reason to

suppose the phenomena of muscle are exceptional. On the contrary,

all the available evidence goes to show that in all the tissues

the oxidation takes place in the tissues and not in the adjoining

blood. It is a remarkable fact, that lymph, serous fluid, bile, urine,

and the other secretions contain no free or loosely combined oxygen,

while the tension of carbonic acid in peritoneal fluid is as high as

six per cent, and in bile and urine is still higher, etc.

All these facts point to the conclusion, that it is the tissues,

and not the blood, which become primarily loaded with carbonic acid,

the latter simply receiving the gas from the former by diffusion;

and that the oxygen which passes from the blood into the tissues is

at once taken up in the same combinations, so that it is no longer

removable by diminished tension.

The production of carbonic acid in the muscle is not directly dependent

on the consumption of oxygen. The muscles produce carbonic acid in

an atmosphere of hydrogen. What is true of muscle is true also of

other tissues and of the body at large.

Oxygen helps to wind up the vital clock; but once wound up, the clock

will go on for a period without further winding (Pflüger).

To sum up, then, the result of respiration in its chemical aspect. As

the blood passes through the lungs, the low oxygen tension of the

venous blood permits the entrance of oxygen from the air of the

pulmonary alveolus, through the thin alveolar wall, through the thin

capillary sheath, through the thin layer of blood plasma, to the red

corpuscles, and the reduced hæmoglobin of the venous blood becomes

wholly, or all but wholly, oxy-hæmoglobin. Hurried to the tissues,

the oxygen, at a comparatively high tension in the arterial blood,

passes largely into the tissues, in which the oxygen tension is always

kept at an exceedingly low pitch, by the fact that the tissues, in

some way at present unknown to us, pack away, at every moment, into

some stable combination each molecule of oxygen which they receive

from the blood. With much, but not all, of its oxy-hæmoglobin reduced,

the blood passes on as venous blood. How much hæmoglobin is reduced

will depend on the activity of the tissue itself. The quantity of

hæmoglobin in the blood is the measure of limit of the oxidizing power

of the body at large; but within that limit the amount of oxidation

is determined by the tissue, and by the tissue alone.

The skin is an excretory tissue, and consists principally of two

layers, an external covering of epithelium, termed the cuticle or

epidermis, and a layer of vascular tissue, named the corium derma or

cutis vera. The integument serves (1) for the protection of deeper

tissues, (2) as a sensitive organ in the exercise of touch, (3) as an

excretory organ, (4) as an absorbing organ, (5) for regulating the

temperature of the body. Within and beneath the corium are imbedded

several organs with special functions, namely, sudoriferous or sweat

glands, sebaceous or fat glands, and hair follicles; and on its

surface are sensitive papillæ. The so-called appendages of the skin,

the hair and nails, are modifications of the epidermis.

Sudoriferous glands: In the middle of each of the transverse furrows

between the papillæ, and irregularly scattered between the bases

of the papillæ in those parts of the surface of the body in which

there are no furrows between them, are the orifices or ducts of the

sudoriferous, or sweat glands, by which it is probable that a large

portion of the aqueous and gaseous materials excreted by the skin are

separated. Each of these glands consists of a small lobular mass,

which appears formed of a coil of tubular gland-duct surrounded by

blood-vessels and imbedded in the subcutaneous adipose tissue. From

this mass the duct ascends, for a short distance, in a spiral manner

through the deeper parts of the cutis, then passing straight, and

then sometimes again becoming spiral, it runs through the cuticle and

opens by an oblique, valve-like apparatus. The sudoriferous glands

are abundantly distributed over the whole surface of the body; but are

especially numerous, as well as very large, in the skin of the palm of

the hand. They are estimated from 2,738 to 3,528 in each superficial

square inch. They are almost equally abundant and large in the skin

of the sole. The glands by which the peculiar odorous matter of the

axilla is secreted form a nearly complete layer under the cutis, and

are like the ordinary sudoriferous glands, except in being larger

and having very short ducts. In the neck and back, where they are

least numerous, the glands amount to 417 on the square inch. The

total number is estimated, at 2,381,248; and supposing the orifice

of each gland to present a surface of 1/54 of a line in diameter (and

regarding a line as equal to 1/10 of an inch) the whole of the glands

would present an evaporating surface of about eight square inches.

Sebaceous glands secrete a peculiar fatty matter. Like the sudoriferous

glands, they are abundantly distributed over most parts of the body.

The quantity of matter which leaves the human body by way of the skin

is very considerable. It is estimated that while 7 grains pass through

the lungs per minute, as much as 11 escape through the skin. The

amount varies extremely. It is calculated that the total amount of

perspiration excreted from the whole body in 24 hours might range

from 2 to 20 kilos.

The total amount of perspiration is affected not only by the condition

of the atmosphere, but also by the nature and quantity of food taken,

the amount of fluid drunk, and the amount of exercise taken. It is

also influenced by the mental condition, by medicines and poisons, by

disease, and by the relative activity of the other excreting organs,

more particularly the kidneys.

The fluid perspiration or sweat, when collected, is found to be a

clear colorless fluid, with a strong and distinctive odor varying

according to the part of the body from which it is taken. Besides

accidental epidermic scales, it contains no structural elements. Its

reaction is generally acid, but in cases of excessive secretion may

become alkaline. The average amount of solids is about 1.81 per cent,

of which about two-thirds consists of organic substances. The chief

normal constituents are (1) sodium chloride (common salt), with small

quantities of other inorganic salts; (2) various acids of the fatty

series, such as fermic, acetic, butyric acid, with probably other

acids--CH2O2-C2H4O2--C4H8O2; (3) neutral fats and cholestrine; (4)

ammonia (NH3) (urea), and possibly other nitrogenous substances.

The average loss by cutaneous and pulmonary exhalation in a minute

is from 17 to 18 grains; the minimum, 11 grains; the maximum, 32

grains; of the average 18 grains 11 pass by the skin and 7 by the

lungs. The maximum loss by exhalation, cutaneous and pulmonary, in

twenty-four hours is about 3 3/4 pounds; the minimum, about 1 1/2

pounds. Valentine found the whole quantity lost by exhalation from

the respiratory and cutaneous surfaces of a healthy man who consumed

daily 40,000 grains of food and drink to be 19,000 grains, or 2 1/2

pounds. Subtracting from this, for the pulmonary exhalation, 5,000

grains, and for the excess of the weight of the exhaled carbonic acid

over that of the equal volume of the inspired oxygen, 2,256 grains,

the remainder, 11,744 grains, or nearly 1 5/7 pounds, may represent

an average amount of cutaneous exhalation in a day.

The Kidneys, two in number, are excretory organs. They are deeply

seated in the lumbar region, one on each side of the vertebral column,

at the back of the abdominal cavity, and behind the peritoneum. The

kidneys measure about 4 inches in length, 2 1/2 inches in breadth,

and 1 1/2 inches in thickness. The left is usually longer and narrower

than the right one. The weight of the kidney is usually stated to be

about 4 1/2 ounces in the male and somewhat less in the female.

The excretory apparatus consists of fine tubules (the tubuli

urineferi), malpighian bodies, blood-vessels, nerves, and lymphatics,

etc.

The kidneys are highly vascular, and receive their blood from the

renal arteries, which are very large in proportion to the organ they

supply. Each artery breaks up into four or five branches, these

again subdivide and break up into capillaries in the substance of

the kidney. The veins arise by numerous venous radicals from the

capillary network of the kidney, as seen near the surface of the

gland, and collect the blood from the capillary plexus around the

convoluted tubules which mainly compose this part, the smaller veins

joining together and ultimately forming a single vein and ending in

the inferior vena cava.

The kidneys are so arranged by their anatomical structure--that of

the cortical and medullary substance, the tubuli urineferi, pyramids,

malpighian bodies, etc.--that they separate from the blood the solids

in a state of solution. The secretion takes place by the agency of

the gland cells, and equally in all the parts of the urine tubes. The

protoplasmic cells which line at least a large portion of the tubuli

urineferi elaborate from the blood certain substances, and discharge

them into the channels of the tubules. All parts of the tubular

system of the kidney take part in the secretion of urine as a whole,

but there is another provision of vessels for a more simple draining

off of the water from the blood when required.

The large size of the renal arteries and veins permits so rapid

a transit of the blood through the kidneys that the whole of the

blood is purified by them. The secretion of urine is rapid in

comparison with other secretions, and as each portion is secreted,

it propels that which is already in the tubes onwards into the pelvis

of the kidney. Thence, through the ureter, the urine passes into the

bladder, into which its rate and mode of entrance has been watched. The

urine does not enter the bladder at any regular rate, nor is there a

synchronism in its movement through the two ureters. In a recumbent

posture the urine collects for a little time in the ureters, then flows

gently, and if the body is raised, runs from them in a stream till they

are empty. Its flow is increased in deep inspiration, or straining,

and in active exercise, and in fifteen or twenty minutes after meals.

Substances taken into the stomach pass very rapidly through the

circulation. It does not take longer than one minute for ferrocyanide

of potassium to pass through. Vegetable substances pass in from

sixteen to thirty-five. Neutral alkaline salts with vegetable acids,

which were generally decomposed in transitu, made the urine alkaline

in twenty-eight to forty-seven minutes. But the time of passage varied

much; and the transit was always slow when the substances were taken

during digestion.

There are really two distinct parts in the kidney--the actively

secreting part, the epithelium of the secreting tubules; and what

maybe called a filtering part, the malpighian bodies.

The specific gravity of urine is 1020--that is, the average human

urine. Urine varies--in the morning before breakfast it is darker,

urina sanguinis; urine secreted shortly after the introduction

of any considerable quantity of fluid into the body, urina potus;

and the urine evacuated immediately succeeding a solid meal of food,

urina cibi. The last kind contains a larger quantity of solid matter

than either of the others, the first and second being largely diluted

with water.

Specific gravity: The morning urine is best calculated for

analysis. The average healthy range may be stated at 1015 in the

winter to 1025 in the summer, and variations of diet and exercise may

make a great difference. In disease, the variations may be greater;

sometimes descending in albuminaria to 1004, and frequently ascending

in diabetes, when the urine is loaded with sugar, to 1050, or even

to 1060.

The whole quantity of urine secreted in twenty-four hours is subject to

variations according to the amount of fluid drunk, and the proportion

of the latter passing off from skin, lungs, and alimentary canal. The

average quantity voided in twenty-four hours by healthy male adults

from twenty to forty years of age amounts to 52 1/2 fluid ounces.

The chemical composition of urine. The average quantity of each

constituent of the urine in 1,000 parts is:

Water (O H2), 967

Urea (C O N2 H4), 14.239

Uric acid (C5 N4 H4 O3), .468

Coloring matter, mucus, and animal

extractive matter, 10.107

{ Sulphates (soda, potash), } 8.185

Salts. { Bisulphates (lime, soda, }

{ magnesia, ammonia), }

{ Chlorides (sodium, potassium), }

Silica, etc., Traces.

---------

1,000.000

Urea is the principal solid constituent of the urine, forming nearly

one-half of the whole quantity of solid matter. It is also the most

important ingredient, since it is the chief substance by which the

nitrogen of decomposed tissue and superfluous food is excreted from

the body.

The salts excreted by the kidneys in 24 hours are:

Urea (C N2 H4 O), 512 grains.

Chloride of sodium (Na Cl), 177   ,,

Phosphoric acid (H3 P O4), 48   ,,

Sulphuric acid (H2 S O4), 31.11   ,,

Uric acid (C5 N4 H4 O3), 8.53   ,,

The substances excreted consist mainly of carbonic acid gas (C O2),

which is expired by the lungs, and urea (C N2 H4 O), which is expelled

by the urine.

These excretions, or expenditures, or waste products of the human

body, present the carbohydrates--starch, sugars, and fats--and the

proteids--meats and albumen--taken into the system as food.

The daily average loss by the expenditure or waste products of the

body is estimated to be about:

Carbon, 4,500 grains.

Nitrogen, 3 to 500 grains.

Besides salts and water.

Of all the elements of the income and outcome, the nitrogen, the

carbon, and the free oxygen of respiration, are by far the most

important. Since water is of use to the body for merely mechanical

purposes, and not as food in the strict sense of the word, the

hydrogen element becomes a dubious one; the sulphur of the proteids,

and phosphorus of the fats, are insignificant in amount; while the

saline matters stand on a wholly different footing from the other

parts of the food, inasmuch as they are not sources of energy, and

pass through the body with comparatively little change.

The correct income will consist of so much nitrogen, carbon, hydrogen,

oxygen, sulphur, phosphorus, saline matters, and water, contained

in the proteids, fats, carbohydrates, salts, and water of the food,

together with the oxygen absorbed by the lungs, skin, and alimentary

canal.

The outcome will consist of: 1. The respiratory products of the lungs,

skin, and alimentary canal, consisting chiefly of carbonic acid and

water, with small quantities of hydrogen and carburetted hydrogen,

these two latter coming exclusively from the alimentary canal;

2. Perspiration, consisting chiefly of water and salts, with urea by

the skin, and other organic constituents of sweat amounting to very

little; 3. The urine, which contains practically all the nitrogen

really excreted by the body, as well as a large quantity of saline

matter and water.

HEAT AND TEMPERATURE.

The average temperature of the human body in those internal parts which

are more accessible, as the mouth and rectum, is from 98.5° to 99.5° F.

The chief circumstances by which the temperature of the healthy body

is influenced are the following:

Age. The average temperature of the new-born babe is only about 1°

F. above that proper to the adult. In old age the temperature rises

again, and approaches that of infancy.

Sex. In the female slightly higher than in the male.

Exercise. Active exercise raises the temperature of the body, through

muscular contraction, etc.

Climate and season. In passing from a temperate to a hot climate,

the temperature of the human body rises slightly, rarely more than 2°

to 3° F. In summer the temperature of the body is a little higher

than in winter, 1/5° to 1/3° F.

Cold alcoholic drinks depress the temperature 1/2° to 1°F.

Warm alcoholic drinks, as well as warm tea and coffee, raise the

temperature about 1/2° F.

In disease, as in pneumonia and typhus, it occasionally rises as high

as 106° or 107° F.

In Asiatic cholera a thermometer placed in the mouth sometimes rises

only to 77° or 79° F.

The temperature maintained by mammalia of an active state of life

averages 101° F. In birds, the average is as high as 107° F., the

highest temperature, 111.25°, being in the species of the linnets, etc.

The sources and distribution of heat. Wherever metabolism of protoplasm

is going on, heat is being generated. All over the body heat is being

set free; more abundantly in the more active tissues, and most of

all in those tissues the metabolism of which leads to little or no

external work. The metabolism of the tissues (including the blood)

and of the food within the alimentary canal is the source of the heat

of the body. But heat, being continually produced, is as continually

being lost, as we have seen, by the skin, urine, and feces. The blood

passing from one part of the body to another, and carrying warmth from

the tissues where heat is being actively generated, to the tissues or

organs where heat is being lost by conduction or evaporation, tends

to equalize the temperature of the various parts and thus maintain

a constant bodily temperature.

Taking the body as a whole, under normal conditions, the chief sources

of the production of heat are the muscles, and the abdominal viscera,

more especially the liver; and of these the liver deserves attention,

inasmuch as it is always at work, whereas the heat produced by the

muscles is at least largely dependent on their contracting, and they

may remain at rest for a considerable period. The brain, too, may be

regarded as a source of heat, since its temperature is higher than

that of the arterial blood with which it is supplied.

Heat is lost by the skin, respiration, feces, etc. The great regulator,

however, is undoubtedly the skin. The more blood passes through the

skin the greater will be the loss of heat by conduction, radiation,

and evaporation. The working of this heat-regulating mechanism is

well seen in the case of exercise. Since every muscular contraction

gives rise to heat, exercise must increase for the time being the

production of heat; yet the bodily temperature rarely rises as much

as a degree C., if at all. By exercise the respiration is quickened

and the loss of heat by the lungs increased. The circulation of blood

is also quickened, and the cutaneous vascular areas becoming dilated,

a large amount of blood passes through the skin. The expenditure of

heat may be tabulated thus:

By the skin, in conducting, radiating, and

evaporating, 77.5 per cent.

Warming expired air, 5.2  ,,

Evaporating the water of respiration, 14.5  ,,

In warming urine, etc., 2.6   ,,

THE CIRCULATION.

The heart is a hollow muscular organ divided by a longitudinal septum

into a right and a left half, each of which is again subdivided by

a transverse constriction into two compartments communicating with

each other, and named auricle and ventricle.

The heart is inclosed in the pericardium and placed behind the

sternum and costal cartilages on the border end or base, by which it

is attached, being directed upwards, backwards, and to the right,

and extending from the level of the fourth to that of the eighth

dorsal vertebra, the apex downwards, forwards, and to the left.

In size, it is about five inches long, three and a half in its

greatest width, and two in its extreme thickness from the anterior

to the posterior surface. The weight is from nine to ten ounces.

The circulation of the blood.--

The body is divided into two chief cavities, the chest or thorax,

and abdomen, by a curved muscular partition called the diaphragm or

midriff. The chest is almost entirely filled with lungs and heart,

the latter being fitted in, so to speak, between the two lungs, nearer

to the front than the back of the chest, and partly overlapped by them.

In the living body the heart and lungs are in constant rhythmic

movement, the result of which is an unceasing stream of air through

the trachea alternately into and out of the lungs, and an unceasing

stream of blood into and out of the heart.

The blood is conveyed away from the heart by the arteries and returned

to it by the veins; the arteries and veins being continuous with each

other, at one end by means of the heart, and at the other by a fine

network of vessels called capillaries. The blood, therefore, in its

passage from the heart passes first into the arteries, then into the

capillaries, and lastly into the veins, by which it is conveyed back

again to the heart--thus completing a revolution, or circulation.

There are two circulations by which all the blood must pass--the one a

shorter circuit from the heart to the lungs and back again, which is

called the pulmonic; the other the larger circuit, from the heart to

all parts of the body and back again, which is called the systemic;

and a subordinate stream of blood, that has been collected by the

blood-vessels of the intestines, passes by means of the portal vein

through the liver, and is called the portal circulation.

The principal force provided for constantly moving the blood on

this course, is that of the muscular substance of the heart; other

assistant forces are (2) those of the elastic walls of the arteries,

(3) the pressure of the muscles among which some of the veins run,

(4) the movements of the walls of the chest in respiration, and (5)

probably to some extent the interchange of relations between the

blood and the tissues which ensues in the capillary system during

the nutritive processes. The right direction of the blood's course

is determined and maintained by the valves of the heart.

The heart is divided into two chief chambers or cavities--right

and left. Each of these chambers is again divided into an upper and

lower portion called respectively auricle and ventricle, which freely

communicate with each other.

The right auricle communicates on the one hand with the veins of the

general system and on the other with the right ventricle. The valvular

curtain between the right auricle and the right ventricle is named

the tricuspid; by it the auricle is guarded from the ventricle. The

ventricle leads directly into the pulmonary artery and this in turn

into the lungs. The pulmonary artery is guarded by three semilunar

valves. The left auricle again communicates on the one hand with the

pulmonary vein and on the other with the left ventricle, which is

guarded by the mitral or bicuspid valve. The left ventricle leads

directly into the aorta, which is also guarded by three semilunar

valves. The aorta is a large artery which conveys the blood to the

general system.

The arrangement of the heart's valves is such that the blood can pass

only in one definite direction, and this is--from the right auricle the

blood passes into the right ventricle, and thence into the pulmonary

artery, by which it is conveyed to the capillaries of the lungs. From

the lungs, the blood, which is now purified and altered in color, is

gathered by the pulmonary veins and taken to the left auricle. From

the left auricle it passes into the left ventricle, and thence into

the aorta, by which it is distributed to the capillaries in every

portion of the body.

The Heart's action. The heart's action in propelling the blood

consists in the successive alternate contractions and dilatations of

the muscular walls of the two auricles and ventricles. The auricles

contract simultaneously; so do the ventricles; their dilatations also

are severally simultaneous; and the contractions of the one pair of

cavities are synchronous with the dilatations of the other.

Valves--Bi and Tricuspid. During auricular contraction the force of the

blood propelled into the ventricle is transmitted in all directions,

but being insufficient to raise the semilunar valves, it is expended

in distending the ventricle and in raising and gradually closing the

auriculo-ventricular valves (tricuspid and bicuspid valves). These

when the ventricle is full form a complete septum (partition) between

it and the auricle.

The arterial or semilunar valves are brought into action by the

pressure of the arterial blood forced back towards the ventricles, when

the elastic walls of the arteries recoil after being dilated by the

blood propelled into them in the previous contraction of the ventricle.

The sounds. When the ear is placed over the region of the heart two

sounds may be heard at every beat of the heart, which follow in quick

succession, and are succeeded by a pause or a period of silence. The

first sound is dull and prolonged; its commencement coincides with the

impulse of the heart and just precedes the pulse at the wrist. The

second is a shorter and sharper sound, with a somewhat flapping

character, and follows close after the arterial pulse.

First sound. The chief cause of the first sound of the heart appears

to be the vibration of the auriculo-ventricular valve, and also,

but to a less extent, of the ventricular walls, and the coats of the

aorta and pulmonary artery, all of which parts are suddenly put into

a state of tension at the moment of ventricular contraction.

The second sound is more complete than that of the first. It is

probably due entirely to the sudden closure and consequent vibration

of the semilunar valves when they are pressed down across the orifice

of the aorta and pulmonary artery.

Pulse. The heart of a healthy adult man in the middle period of life

acts from seventy to seventy-five times per minute. The frequency of

the heart's action gradually diminishes from the commencement to near

the end of life.

In persons of sanguine temperament, the heart acts somewhat more

frequently than in those of the phlegmatic; and in the female sex

more frequently than in the male; in children, more frequently still.

Capacity. The capacity of the two ventricles is probably exactly the

same. From the mean of various estimates taken, it may be inferred

that each ventricle is able to contain on an average about three

ounces of blood, the whole of which is impelled into the respective

arteries at each contraction.

Every time the ventricles contract three ounces of blood are pumped

out of the heart into the lungs and heart respectively.

Calculating seventy pulses per minute, the quantity of blood passing

through the heart would be about 211 ounces, or 14 1/4 pints per

minute; or 895 pints per hour, or 21,480 pints in 24 hours.

Velocity. The velocity of the stream of blood is greater in the

arteries than in any other part of the circulatory system, and in

them it is greatest in the neighborhood of the heart and during

the ventricular systole; the rate of movement diminishes during the

diastole of the ventricles, and in the parts of the arterial system

most distant from the heart. The rate is calculated to be about from

10 to 12 inches per second in the large arteries near the heart.

THE BLOOD.

Blood is a tissue of which the red corpuscles are the essential and

active elements, while the plasma is the liquid matrix. There are

two kinds of corpuscles, the white and the red. The protoplasm of the

white corpuscles is native indifferentiated protoplasm, in no respect

fitted for any special duty, as far as we know at present. The white

corpuscles are in reality embryonic structures, concerned chiefly in

the production of other forms, such as red corpuscles, and it may be

under certain conditions various elements of the other tissues. The red

corpuscles have a definite respiratory function. But these form a part

only of the blood. The largest portion of the blood, the whole mass

of the plasma, is an unorganized fluid with no proper physiological

(vital) properties of its own. Its function is to serve as the great

medium of exchange between all the tissues of the body. Just as the

whole organism lives on the things around it, its air and its food,

so the several tissues live on the complex fluid by which they are

all bathed and which is to them their immediate air and food.

Blood within the living vessel is a fluid; but when shed, or after

the death of the vessels, becomes solid by the process known as

coagulation. The average specific gravity of human blood is 1056,

varying from 1045 to 1075 within the limits of health. It has an

alkaline reaction, which in shed blood rapidly diminishes up to the

onset of coagulation.

Blood may, in general terms, be considered as consisting by weight of

more than one-third and less than one-half of corpuscles, the rest

being plasma, the corpuscles being supposed to retain the amount of

water proper to them. Human blood: corpuscles 513, plasma 487. The

average quantity of fibrine in the human blood is said to be two

per cent.

Composition of serum: In 100 parts there are in round numbers:

Water, 90 parts.

Proteid substance, 8 to 9   ,,

Fat extractives and saline matter, 2 to 1   ,,

Of the proteid substances the great mass consists of the so-called

serum-albumen.

Composition of red corpuscles: The red corpuscles contain less water

than the serum. In 100 parts of red corpuscle there are:

Water, 56.5

Solid, 43.5

The solids are almost entirely organic matter, the inorganic salts

in the corpuscles amounting to less than 4 per cent. In 100 parts of

dried organic matter of the corpuscles of human blood there are:

Hæmoglobin, 90.54

Proteid substance, 8.67

Lecithin, .54

Cholestrin, .25

The blood is distributed as follows in round numbers:

In the heart, lungs, large arteries and veins, About one-fourth.

In the liver,  ,,      ,,

In the skeletal muscles,  ,,      ,,

In the other organs,  ,,      ,,

The average proportion of the principal constituents of the blood in

1,000 parts is:

Water, 784

Red corpuscles (solid residue), 130

Albumen serum, 70

Saline matter, 6.03

Extractive fatty matter, 7.77

Fibrine, 2.20

The chemical composition of hæmoglobin is:

Carb. Hyd. Iron. Nit. Oxy. Sulph.

54.2 7.2 0.42 16.0 21.5 6.7

Mucine, 52.2 7.0 12.6 28.2

Proteids, 51.5 6.9 15.2 20.9 0.

to 54.5 to 7.3 to 17.0 to 23.5 to 2.0

THE ORGANS OF RESPIRATION.

The principal organs of respiration consist of larynx, trachea,

bronchi, lungs.

The larynx is affixed to the upper end of the windpipe, and is not

only the entrance for air into the respiratory organs from the pharynx,

but also the organ of voice.

The trachea measures from four inches to four inches and a half in

length, and from three-quarters of an inch to one inch in width; but

its length and width are liable to continual variations, according

to the position of the larynx and the direction of the neck.

The trachea divides into two branches, called bronchi, right and

left. The right bronchus, wider and shorter than the left, measuring

about an inch in length, passes outwards almost horizontally into the

root of the right lung on a level with the fourth dorsal vertebra. The

left bronchus, smaller in diameter but longer than the right, being

nearly two inches in length, inclines downwards and outwards to reach

the root of the right lung, which it enters on a level with the fifth

dorsal vertebra--that is, about an inch lower than the right bronchus.

The lungs, placed one on the right and the other on the left of the

heart and large vessels, occupy by far the larger part of the cavity

of the chest, and during life are always in accurate contact with the

internal surface of its walls. Each lung is attached at a comparatively

small part of its flattened inner or median surface by a part named

the root and by a thin membranous fold, which is continued downwards

from it.

The pleuræ are serous membranes forming two shut sacs, quite distinct

from each other, which line the right and left side of the thorax,

forming by their approximation in the middle line the mediastinal

partition, and are reflected each upon the root and over the entire

free surface of the corresponding lung.

The lungs. Each lung is irregularly pyramidal or conical, with its

base downwards, and one side (the inner) much flattened. The broad

concave base is of a semi-lunar form, and rests upon the arch of the

diaphragm. The apex is blunt, and reaches into the root of the neck,

above the first rib, where it is separated from the first portion of

the subclavian artery by the pleural membrane.

The lungs vary much in size and weight, according to the quantity of

blood and mucous or serous fluid they may happen to contain, which

is greatly influenced by the circumstances immediately preceding

death, as well as other causes. The weight of both lungs together,

as generally stated, ranges from 30 to 48 ounces, the more prevalent

weights being found between 36 and 42 ounces. The proportion borne

by the right lung to the left is nearly 22 ounces to 20, taking

the combined weight of the two at 42 ounces. The lungs are not only

absolutely heavier in the male than in the female, but appear to be

heavier in proportion to the weight of the body. The general ratio

between the weight of the lungs and body in the adult fluctuates

between one to thirty-five and one to fifty.

The average weight in twenty-nine cases, male and female:

Male. Female.

Right lung, 24 ounces. 17 ounces.

Left lung, 21   ,,    15   ,,

--------- ---------

45 ounces. 32 ounces.

The proportionate weight of the lungs to the body is:

Male. Female.

1 to 37 1 to 34

The substance of the lungs is of a light porous spongy texture, and

when healthy is buoyant in water. Specific gravity, 0.126; deprived

of air, 1.056.

When pressed between the fingers, the lungs impart a crepitant

sensation, which is accompanied by a peculiar noise, both effects

being caused by the air contained in the tissue. On cutting the lung

the same crepitation is heard.

The pulmonary tissues are endowed with great elasticity, in consequence

of which the lungs collapse to about one-third of their bulk when

the thorax is opened.

The root of each lung consists of bronchi, arteries, and veins,

together with the nerves, lymphatic vessels, and glands, connected

by areolar tissue, and inclosed in a sheath of the pleura.

Respiration consists of an expiration and an inspiration. The air

passes in through the nose or mouth, through the larynx, trachea,

bronchi, into the lungs.

Inspiration: By the contraction of certain muscles, the cavity of the

thorax is enlarged; in consequence the pressure of the air within the

lungs becomes less than that of the air outside the body, and this

difference of pressure causes a rush of air through the trachea into

the lungs until an equilibrium of pressure is established between the

air inside and that outside the lungs. This constitutes inspiration.

Expiration: Upon the relaxation of the inspiratory muscles (the

muscles whose contraction has brought about the thoracic expansion),

the elasticity of the chest walls and lungs, aided by the contraction

of certain muscles and other circumstances, causes the chest to return

to its original size, or even become smaller. In consequence of this

the pressure within the lungs now becomes greater than that outside,

and thus air rushes out of the trachea, until equilibrium is once

more established. This constitutes expiration.

The inspiratory and expiratory act together form a respiration.

The fresh air introduced into the upper part of the pulmonary passages

by the inspiratory movement contains more oxygen and less carbonic

acid than the old air previously present in the lungs. By diffusion the

new or tidal air, as it is frequently called, gives up the oxygen to,

and takes carbonic acid from, the old or stationary air, and thus

when it leaves the chest in expiration has been the means both of

introducing oxygen into and of removing carbonic acid from it. By

this ebb and flow of the tidal air and the diffusion between it and

the stationary air, the air in the lungs is being continually renewed,

through the alternate expansion and contraction of the chest. In what

may be considered normal breathing, the respiratory act is repeated

about seventeen times a minute; and the duration of the inspiration

as compared with that of the expiration and such pause as exists,

is about as ten to twelve.

When the ordinary respiratory movements prove insufficient to effect

the necessary changes in the blood, their rhythm and character become

changed. Normal respiration gives place to labored respiration, and

this in turn to dyspnoea, which unless some restorative event occurs

terminates in asphyxia.

Changes of the air in respiration:

1. The temperature of the expired air is variable, but under ordinary

circumstances is higher than that of the inspired air.

2. The expired air is loaded with aqueous vapor.

3. The expired air contains about 4 to 6 per cent less oxygen and about

4 per cent more carbonic acid than the inspired air, the quantity of

nitrogen suffering but little change. Thus:

Oxygen. Nitrogen. Carbon.

Inspired air contains 20.81 79.15 .04

Expired ,,     ,,    16.033 79.557 4.380

While the air in passing in and out of the lungs is thus robbed of a

portion of its oxygen, and loaded with a certain quantity of carbonic

acid, the blood as it streams along the pulmonary capillaries undergoes

important correlative changes. As it leaves the right ventricle it

is venous blood of a dark purple or maroon color; when the blood

has passed through the lungs and falls into the left auricle, it

is arterial blood of a bright scarlet hue. In passing through the

capillaries of the body from the left to the right side of the heart,

it is again changed from the arterial to the venous condition.

The average composition of this gas in the two kinds of blood is as

follows. From 100 volumes may be obtained:

Oxygen. Carbonic Acid. Nitrogen.

Of arterial blood, 20 (16) vol. 39 (30) vol. 1 to 2 vol.

Of venous blood, 8-12 (6 to 10) 46 (35) vol. 1 to 2 vol.

Oxygen plays a most important role on this terrestrial globe. Life,

health, and food depend on it. This element penetrates, pervades,

everything and everywhere, unites and disunites with all other

elements, preserves and destroys. While its absence from a living

being, whether plant or animal, is death.

When a liquid such as water is exposed to an atmosphere containing a

gas such as oxygen, some of the oxygen will be dissolved in the water,

that is to say will be absorbed from the atmosphere. The quantity which

is so absorbed will depend on the quantity of oxygen which is in the

atmosphere above; that is to say, on the pressure of the oxygen; the

greater the pressure of the oxygen, the larger the amount which will

be absorbed. If, on the other hand, water containing a good deal of

oxygen dissolved in it be exposed to an atmosphere containing little or

no oxygen, the oxygen will escape from the water into the atmosphere.

The Creation of God · 第 10 / 21 章