The Circulation

Text Book of Biology, Part 1: Vertebrata by H. G. Wells, is part of the HackerNoon Books Series. You can jump to any chapter in this book here. The Circulation

The Circulation

Section 34. The next thing to consider is the distribution of the food material absorbed through the walls of the alimentary canal to the living and active parts of the body. This is one of the functions of the series of structures-- heart and blood-vessels, called the circulation, circulatory system, or vascular system. It is not the only function. The blood also carries the oxygen from the lungs to the various parts where work is done and kataboly occurs, and it carries away the katastases to the points where they are excreted-- the carbon dioxide and some water to the lungs, water and urea to the kidneys, sulphur compounds of some kind to the liver.

Section 35. The blood (Figure 4, Sheet 2) is not homogeneous; under the low power of the microscope it may be seen to consist of--

(1.) a clear fluid, the plasma, in which float--

(2.) a few transparent colourless bodies of indefinite and changing shape, and having a central brighter portion, the nucleus with a still brighter dot therein the nucleolus-- the white corpuscles (w.c.), and

(3.) flat round discs, without a nucleus, the red corpuscles (r.c.), greatly more numerous than the white.

Section 36. The chyle of the lacteals passes, as we have said, by the thoracic duct directly into the circulation. It enters the left vena cava superior (l.v.c.s.) near where this joins the jugular vein (ex.j.) (see Figure 1, Sheet 2, th.d.) and goes on at once with the rest of the blood to the heart. The small veins of the villi, however, which also help suck up the soluble nutritive material, are not directly continuous with the other body veins, the systemic veins; they belong to a special system, and, running together into larger and larger branches, form the lieno gastric (l.g.v.) and mesenteric (m.v.) veins, which unite to form the portal vein (p.v.) which enters the liver (l.v.) and there breaks up again into smaller and smaller branches. The very finest ramifications of this spreading network are called the (liver) capillaries, and these again unite to form at last the hepatic vein (h.v.) which enters the vena cava inferior (v.c.i.), a median vessel, running directly to the heart. This capillary network in the liver is probably connected with changes requisite before the recently absorbed materials can enter the general blood current.

Section 37. The student has probably already heard the terms vein and artery employed. In the rabbit a vein is a vessel bringing blood towards the heart, while an artery is a vessel conducting it away. Veins are thin-walled, and therefore flabby, a conspicuous purple when full of blood, and when empty through bleeding and collapsed sometimes difficult to make out in dissection. They are formed by the union of lesser factors. The portal breaks up into lesser branches within the liver. Arteries have thick muscular and elastic walls, thick enough to prevent the blood showing through, and are therefore pale pink or white and keep their round shape.

Section 38. The heart of the rabbit is divided by partitions into four chambers: two upper thin-walled ones, the auricles (au.), and two lower ones, both, and especially the left, with very muscular walls, the ventricles (vn.). The right ventricle (r.vn.) and auricle (r.au.) communicate, and the left ventricle (l.vn.) and auricle (l.au.).

Section 39. The blood coming from all parts of the body, partly robbed of its oxygen and containing much carbon dioxide and other katastases, enters the right auricle of the heart through three great veins, the median vena cava inferior from the posterior parts of the body, and the paired venae cavae superiores from the anterior. With the beating of the heart, described below, it is forced into the right ventricle and from there through the pulmonary artery (p.a.) seen in the figure passing under the loop of the aorta (ao.) to the lungs.

Section 40. The lungs (lg. Figure 1, Sheet 1) are moulded to the shape of the thoracic cavity and heart; they communicate with the pharynx by the trachea (tr. in Figure 1, Sheet 1) or windpipe, and are made up of a tissue of continually branching and diminishing air-tubes, which end at last in small air-sacs, the alveoli. The final branches of the pulmonary arteries, the lung capillaries, lie in the walls of these air-sacs, and are separated from the air by an extremely thin membrane through which the oxygen diffuses into, and the carbon dioxide escapes from, the blood.

Section 41. The mechanism of respiration will be understood by reference to Figure 3, Sheet 2. It will be noted, in dissecting that the lungs have shrunk away from the walls of the thorax; this collapse occurs directly an aperture is made in the thorax wall, and is in part due to their extreme elasticity. In life the cavity of the thorax forms an air-tight box, between which and the lungs is a slight space, the pleural cavity (pl.c.) lined by a moist membrane, which is also reflected, over the lungs. The thorax wall is muscular and bony, and resists the atmospheric pressure on its outer side, so that the lungs before this is cut through are kept distended to the size of the thoracic cavity by the pressure of the air within them. In inspiration (or breathing-in) the ribs are raised by the external intercostal (Anglice, between-ribs, e.i.c.m.) and other allied muscles, and the diaphragm (dia.) contracts and becomes flatter; the air is consequently sucked, in as the lungs follow the movement of the thorax wall. In expiration the intercostals and diaphragm relax and allow the elastic recoil of the lungs to come into play. The thoracic wall is simultaneously depressed by the muscles of the abdominal area, the diaphragm thrust forwards, as the result of the displacement and compression of the alimentary viscera thus brought about. (r.r.r. in the Figure mark ribs.)

Section 42. The oxygen and carbon dioxide are not carried in exactly the same way by the blood. The student will know from his chemical reading that neither of these gases is very soluble, but carbon dioxide is sufficiently so in an alkaline fluid to be conveyed by the liquid plasma. The oxygen however, needs a special portative mechanism in the colouring matter of the red corpuscles, the haemoglobin, with which it combines weakly to form oxy-haemoglobin of a bright red colour, and decomposing easily in the capillaries (the finest vessels between the arteries and veins), to release the oxygen again. The same compound occurs in all true vertebrata, and in the blood-fluid of the worm; in the crayfish a similar substance, haemocyanin, which when oxygenated is blue, and when deoxydized colourless, discharges the same function.

Section 43. The blood returns from the lungs to the left auricle (l.au.) by the pulmonary veins, hidden in the Figure by the heart, passes thence to the thick-walled left ventricle (l.vn.), and on into the aorta (ao.).

Section 44. The beating of the heart is, of course, a succession of contractions and expansions of its muscular wall. The contraction, or systole, commences at the base of the venae cavae and passes to the auricles, driving the blood before it into the ventricles, which then contract sharply and drive it on into the aorta or pulmonary artery; a pause and then a dilatation, the diastole follows. The flow of the blood is determined in one direction by the various valves of the heart. No valves occur in the opening of the superior cavae but an imperfect one, the Eustachian valve, protects the inferior cava; the direction of the heart's contraction prevents any excessive back-flow into the veins, and the onward, tendency is encouraged by the suck of the diastole of the ventricles. Between the left ventricle and auricle is a valve made up of two flaps of skin, the mitral valve, the edges of the flaps being connected with the walls of the ventricle through the intermediation of small muscular threads, the chordae tendinae, which stretch across its cavity to little muscular pillars, the papillary muscles; these attachments prevent the mitral valve from flapping back into the auricle, and as the blood flows into and accumulates in the ventricle it gets behind the flaps of the valve and presses its edges together. When the systole of the ventricle occurs, the increased, tension of the blood only closes the aperture the tighter, and the current passes on into the aorta, where we find three watch-pocket valves, with the pocket turned away from the heart, which are also closed and tightened by any attempt at regurgitation (back-flow). A similar process occurs on the right side of the heart, but here, instead of a mitral valve of two flaps between auricle and ventricle, we have a tricuspid valve with three. The thickness of the muscular walls, in view of the lesser distance through which it has to force the blood, -are- [is] less for the right ventricle than the left.

Section 45. The following are the chief branches of the aorta. The student should be able to follow them with certainty in dissection; they are all displayed in the Figure; but it must not be imagined for a moment that familiarity with this diagram will obviate the necessity for the practical work; (in.) is the innominate artery; it forks into (s.cl.a.) the right subclavian, and (r.c.c.) the right common carotid. Each carotid splits at the angle of the jaw into an internal and an external branch. The left common carotid, (l.c.c.) arises from the base of the innominate,* (l.s.cl.a.) the left subclavian, directly from the aorta. The aorta now curves round to the dorsal middle line, and runs down as seen in Figure 1, Sheet 1 (d.ao.) and Figure 1, Sheet 2 (d.ao.). Small branches are given off to the ribs, and then comes the median coeliac (coe.a.) to the stomach and spleen, the median superior mesenteric (s.mes.a.) to the main portion of the intestine, and the inferior mesenteric (p.m.a.) to the rectum. Note that no veins to the inferior vena cava correspond to these arteries-- the blood they supply going back by the portal vein (p.v.). The paired renal arteries (r.a.) supply the kidneys, and the common iliacs (c.il.a.) the hind legs, splitting into the internal iliacs (i.il.a.) and the femoral (f.).

{Lines from Second Edition only.}
[The student should note that the only arteries in the middle line are those supplying the alimentary canal.]

{Lines from First Edition only.}
* -The figure is inaccurate, and represents the left common carotid as arising from the aortic arch.-

Section 46. The distribution of the veins of the rabbit has only a superficial parallelism with arteries. The chief factors of vena cava inferior are the hepatic vein (h.v.), which receives the liver blood, the renal veins (r.v.), from the kidneys, the ilaeo-lumbar, from the abdominal wall, and the external (e.il.v.) and internal ilias (i.il.v.); with the exception of the renal veins none of these run side by side with arteries. The superior cavae (r. and l.v.c.s.) are formed by the union of internal (i.j.) and external jugular (e.j.) veins with a subclavian (s.cl.v.) from the fore limb. The term pre-caval vein is sometimes used for superior cava. The attention, of the student is called to the small azygos vein (az.) running into the right vena cava superior, and forming the only asymmetrical (not-balancing) feature of the veins in front of the heart; it brings blood back from the ribs of the thorax wall, and is of interest mainly because it answers to an enormous main vessel, the right post-cardinal sinus, in fishes. There are spermatic arteries and veins (s.v. and a.) to the genital organs. All these vessels should be patiently dissected out by the student, and drawn.

Section 47. Between the final branches of the arteries and the first fine factors of the veins, and joining them, come the systemic capillaries. These smallest and ultimate ramifications of the circulation penetrate every living part of the animal, so that if we could isolate the vascular system we should have the complete form of the rabbit in a closely-meshed network. It is in the capillaries that the exchange of gases occurs and that nutritive material passes out to the tissues and katastases in from them; they are the essential factor in the circulatory system of the mammal-- veins, arteries, and heart simply exist to remove and replace their contents. The details of the branching of the pulmonary artery and the pulmonary veins need not detain us now.

Section 48. Summarising the course of the circulation, starting from the right ventricle, we have-- pulmonary artery, pulmonary capillaries, pulmonary vein, left auricle, left ventricle, aorta, arteries, and systemic capillaries. After this, from all parts except the spleen and alimentary canal, the blood returns to systemic veins, superior or inferior cavae, right auricle, and right ventricle. The blood from the stomach spleen, and intestines however, passes via {through} the portal vein to the liver capillaries and then through the hepatic vein to inferior cava, and so on. Material leaves the blood to be excreted in lungs, kidneys, by the skin (as perspiration), and elsewhere. New material enters most conspicuously;

(a) by the portal veins portal veins and

(b) by the thoracic duct and left superior cava.

Section 49. The following table summarises what we have learnt up to the present of the physiology of the Rabbit, considered as a mechanism using up food and oxygen and disengaging energy:--

About HackerNoon Book Series: We bring you the most important technical, scientific, and insightful public domain books.

This book is part of the public domain. H. G. Wells (2007). Text Book of Biology, Part 1: Vertebrata. Urbana, Illinois: Project Gutenberg. Retrieved October 2022, from https://www.gutenberg.org/files/21781/21781-h/21781-h.htm

This eBook is for the use of anyone anywhere at no cost and with almost no restrictions whatsoever. You may copy it, give it away or re-use it under the terms of the Project Gutenberg License included with this eBook or online at www.gutenberg.org, located at https://www.gutenberg.org/policy/license.html.