Part 2
That the nucleus is the formative center of the cell is indicated by the following, among many facts: If a unicellular animal, such as =Stylonychia= (Fig. 2), for instance, be broken up into several fragments, it will be observed that some of the fragments are nucleated and others non-nucleated. The nucleated fragments have the power of quickly healing the wounds on them, regenerating the missing parts, and thus restoring the mutilated fragments to perfect individuals. These nucleated fragments have the power to perform all the activities of the perfect animal. The non-nucleated portions, on the other hand, cannot undergo regeneration. They cannot digest food, or grow or secrete substances as the nucleated fragments can. They can simply live for awhile, responding to stimuli and moving about. They finally perish.
Having mentioned in a general way some of the wonderful powers of cells, it will be well now to describe briefly a few of the _unicellular plants and animals_ that can be so easily obtained and studied in warm weather, and which may thus serve as illustrations of the powers of nucleated pieces of protoplasm or cells. Many unicellular plants and animals can be obtained in summer from the superficial ooze on the bottom of slow-running streams and also on the under surfaces of the leaves of water plants, a study of which will be of the greatest value and interest.
=Amœba proteus= (Fig. 3). This little unicellular animal, which belongs to the Rhizopod type, is very common in ponds and streams in warm weather. In the resting state it is spherical in form, but when active its form is as changeable as the fabled =Proteus=, hence its name, _Amœba proteus_. This little creature is a naked piece of protoplasm, with its outer layer differentiated into a firmer and pellucid part called the _ectoplasm_ (Fig. 3, ec); its interior, the _endoplasm_ (en), is quite granular and much more fluid, the granular particles moving quite freely upon one another when the animal changes its shape. The superficial portion of the endoplasm is firmer than its more central parts, and graduates insensibly into the more consistent ectoplasm.
[Illustration: FIG. 3.—Amœba proteus: n, nucleus; cv, contractile vesicle; ec, ectoplasm; en, endoplasm; p, pseudopodia.]
In the periphery of the granular endoplasm, and adherent to the inner surface of the ectoplasm, is a clearly defined _nucleus_ (n). When most distinctly seen, it presents the appearance of a clear vesicle surrounding a solid and more or less spherical nucleolus. A _contractile vacuole_ (cv) is also uniformly present, located in the endoplasm. The creature has the power of putting out projections (p) from the surface called false feet (_pseudopodia_). Sometimes the protrusion consists of ectoplasm alone, but more commonly endoplasm extends into it, when a current of granules will be observed moving from the more central portions of the Amœba into its protrusion, whilst from some other protrusion that is being withdrawn a similar current may set towards the center of the body, and thus the animal moves, in a creeping manner, from place to place. While moving about in this way the little animal comes across other one-celled creatures, such as _Desmids_ and _Diatoms_, seizing them and forcing them through its ectoplasm into the endoplasm, where the nutritious parts are digested and assimilated. After the animal has taken its prey through its ectoplasm, no break in the continuity of the ectoplasm remains, but the parts immediately come together in a perfect manner. After it has abstracted all the nutriment from its prey, the Amœba casts away from it the parts that are indigestible.
[Illustration: FIG. 4.—Rotalia Freyeri: a many-shelled Foraminifer, or a colony of many single-shelled Foraminifera, with pseudopodia extended.]
=Foraminifera.= These are little protoplasmic unicellular animals that have the power of secreting for themselves more or less complex envelopes composed of _limestone_. They may be single, as in _Lagena_, or composed of a number of individuals with the shells cemented together as in Globigerina or _Rotalia_ (Fig. 4). They have played a part of vast importance in the geological development of the world. Their myriads of shells remaining at the bottom of seas millions of years after the little protoplasmic bodies have perished, they have been consolidated into vast expanses of limestone rocks, and finally uplifted into such formations as the huge chalk cliffs of England.
=Osteoblasts and Osteoclasts.= These cells are naked pieces of protoplasm, the latter much the larger and having many nuclei. They are concerned in some of the most interesting phenomena of many growing animals. Just as the Foraminifera have the power of forming complex aggregations of limestone shells, so the Osteoblasts have the power to construct the bones of animals. And when a bone is broken as the result of accident, these little cells do the mending. While the Osteoblasts are _bone-formers_, the Osteoclasts are _bone-destroyers_. It is very curious that little specks of living jelly, like these Osteoclasts, should have the power of destroying hard tissue like bone, but such is the fact. These Osteoclasts can, by their wonderful chemical processes, liquefy and absorb, and by these means destroy, ivory pegs that are driven into living bone. They are the agents by which the roots of children’s milk teeth are destroyed, so that the crowns of the teeth are shed and the way paved for the appearance of the permanent teeth. The wonderful activity of these little Osteoblasts and Osteoclasts is well exemplified in the growth and shedding of the antlers of deer. While these antlers are growing in the spring, they are covered with a delicate skin, technically called “velvet.” This velvet is very sensitive and quite warm from the nutrient blood circulating through it. In it are hundreds and thousands of busy, living Osteoblasts that work together under some mysterious, directing or coördinating agency, to build up the splendid beams, tynes and snags that constitute the antlers, which in many deer of the Rocky Mountains reach such a size that a man may walk under the archway made by setting the shed antlers up on their points. No hive of bees is busier or more replete with active life than the antler of a stag as it grows beneath the warm, soft velvet, through the agency of the Osteoblasts.
The building of the antlers by these little agents continues through the spring and summer. In the autumn the Osteoblasts cease their activity and die; the delicate, sensitive velvet dries and peels off, leaving the dead, hard, bony substance exposed, and they now become weapons adapted for fighting. This is the season when the stags challenge one another to single combat, the hinds standing timidly by to be taken by the victor as his mates. When the loves and battles of the autumn are over and the mating is completed, the antlers no longer serve a useful purpose, and they are shed. The shedding is accomplished through the agency of the bone-destroyers, the little jelly-like cells called Osteoclasts.
=Bacteria= are exceedingly minute specks of naked protoplasm. They are unicellular plants. Some of them are harmless to mankind; some are very useful to him, and others are his deadly enemies. Many of them are concerned in the production of the infectious diseases. They do so by elaborating various chemical products that are virulent poisons, hence these products are called toxines; when taken up by the blood, they are carried to various parts of the body. In this manner they cause the particular symptoms that are characteristic of a special infectious disease. Why is it that some persons, on exposure to an infectious disease, contract the malady while others similarly exposed do not? In other words, what gives immunity to disease? The explanation is probably as follows: Just as the invading bacteria have the power of secreting _toxines_, so the cells of the body, normally, have the power of elaborating chemical products that are antidotes to the toxines, and are appropriately called _antitoxines_. Infectious diseases and immunity from them, are the result of a contest between the invading bacteria and the protecting cells of the body. If the bacteria secrete toxines in greater quantities than can be neutralized by the cells of the body, we have disease; if the reverse occur, we have immunity.
The =white blood-corpuscles= (cells) also take part in this warfare. They have the power of traveling, in virtue of their amœboid movements, from the blood to the part invaded by the bacteria. Here a contest takes place between them, the corpuscle takes the bacteria into its interior, and either kills them or is itself killed. The result of this contest helps to produce either immunity or infection.
=Tetanus bacillus= is a cell shaped like a slender rod. It has the power of secreting a poison which, when introduced into the body, produces convulsions and other symptoms of lockjaw. These much resemble those induced by strychnine poisoning.
=Bacillus diphtheriæ= is an exceedingly small unicellular plant, and has the power of producing a poison called _toxalbumin_, which is analogous to the poison of certain venomous serpents. It is the speck of protoplasm through whose activity diphtheria is caused.
Many useful bacteria have the power of so acting on dead organic bodies as to decompose them, the three most conspicuous end-products of this decomposition being water, carbonic oxide and ammonia. When the dead bodies are decomposed in the soil there are other bacteria, in addition, that have the power of further acting on the ammonia, causing its oxidation and producing nitrous and nitric acids and their salts. The unicellular plants that bring about these changes are the _nitrifying bacteria_. Conspicuous illustrations of the functional activity of these little naked pieces of protoplasm are seen in the immense saltpeter beds of Peru and Chili, where, from the enormous fecal accumulations of sea-fowls, the immense quantities of nitrates are produced that supply the commercial world.
[Illustration: FIG. 5.—Difflugia Pyriformis.]
=Arcella=, of which there are many species, is a unicellular animal whose protoplasmic body has secreted from its surface an enclosing “test” that is composed of a _horny membrane_, resembling very much in constitution the chitin which gives firmness to the integuments of insects. This creature is commonly discoidal in shape, with one face arched and the other flat, an aperture being situated in the center of the flat side through which the creature may thrust its pseudopodia or withdraw them. The surface of the testaceous covering is often marked with a regular but minute and attractive pattern. In =Difflugia= (Fig. 5), the test is somewhat pitcher-shaped, and is mostly made up (by the constructive activity of the protoplasm) of exceedingly small particles of shell and gravel cemented together. Many testaceous amœbans form tests of singular beauty and remarkable regularity. In some of the animals the minute plates of which the tests are formed have been picked up from the surface over which the animals crawl, and are cemented into various charming patterns; and in other cases they are formed by secretion from their own bodies. In =Quadrula symmetrica= the protoplasmic body has constructed a pear-shaped testaceous covering, of complete transparence-like glass, composed of a great number of square plates touching each other by their edges. The protoplasmic body of the animal does not entirely fill the test, the intervening space being occupied by a clear liquid and traversed by bands of protoplasm. A clear, large spherical nucleus is seen in the part farthest from the pseudopodia. It contains a dark and well-defined nucleolus. In front of the nucleus two contractile vesicles are to be observed. The pseudopodia in these creatures, it must be remembered, are not appendages, but lobate protrusions of the protoplasmic body, are few in number, rounded, short and broad.
=Diatoms= are unicellular plants, isolated or aggregated together, that have the power of constructing flint coverings, often of great complexity and charming pattern. The tracings on many of these flint coverings are so constant and small, that they are frequently employed for the purpose of testing the power of modern compound microscopes. In various parts of the world vast deposits of Diatoms have been discovered. The most remarkable of these for extent, as well as for the beauty and number of the species contained in it, is that on which the city of Richmond, in Virginia, is built, which is over thirty feet deep and extends for many miles.
[Illustration: FIG. 6.—Noctiluca miliaris. A, dorsal view; B, side view; n, nucleus; f, flagellum; a, entrance to atrium; b, atrium; o, œsophagus; r, superficial ridge.]
=Noctiluca miliaris= (Fig. 6) is a very large unicellular, flagellate animal. It is spheroidal in form, and has an average diameter of not quite one-half a millimeter. It is just large enough to be observed by the unaided eye when the water in which the animal may be swimming is contained in a glass jar held up to the light. It has a tail-like appendage (flagellum) by which the animal moves about. Along one side of the cell is a meridional groove resembling that of a peach, and leading into a deep depression of the surface termed the atrium (Fig. 6, B, b). It is from the shallow commencement of this depression that the flagellum (Fig. 6, f) originates. At the base of the flagellum the depression sinks down to the mouth (o). A slightly elevated ridge (r) extends along the opposite meridian and commences with a bifurcation at that end of the atrium farthest from the flagellum. The mouth opens into a short œsophagus, which leads down directly to the central protoplasmic mass. The central protoplasmic mass sends off branching prolongations of its substance in all directions, the ramifications of which freely inosculate. The farther these ramifications extend out to the periphery, the thinner they become, until finally a protoplasmic network of extreme tenuity is formed immediately under the enveloping membrane of the cell. In addition to these ramifying prolongations, the central protoplasmic mass sends off a thin, broad, irregular extension to the superficial ridge and coalesces with it. Near the central protoplasmic mass is seen the nucleus (n).
The flagellum is a flattened, whip-like filament, having a striated appearance, and gradually tapers from the base to its extremity. It slowly bends over five or six times a minute to the mouth, and then, more slowly still, bends away again. It is through the movements of the flagellum that particles of food are driven into the mouth and down the œsophagus into the central protoplasmic mass. In this mass and its extensions the food is digested and assimilated.
This little one-celled animal has the power, through its special chemical activities, of manufacturing and emitting light. It is through the agency of myriads of these little creatures that the diffused luminosity of some seas is produced and can be observed at night. The Noctiluca is very transparent, and for this reason it is a particularly favorable subject for the study of its luminosity or phosphorescence. They can be obtained by the tow-net in unlimited quantities from the sea and transferred into a jar of sea water. Here they soon rise to the surface, forming a thick layer. If the jar be placed in the dark and agitated in the slightest degree, there is an instantaneous display of light, which is of a beautiful greenish tint. The light emitted by the Noctiluca is so vivid that it can even be observed in ordinary lamp-light. This phosphorescence is only of an instant’s duration, and a short rest is necessary for its renewal. The special locality for the formation of the phosphorescence is in the very fine protoplasmic network, which lines the external structureless membrane or cell wall. These wonderful little Noctilucæ may well be figuratively called the fire-flies of the ocean.
[Illustration: FIG. 7.—Gromia oviformis with protoplasmic threads (pseudopodia) extended and forming an elaborate network in which a captured unicellular organism is seen; d, diatom captured; p, protoplasm containing captured diatoms; s, shell.]
=Gromia oviformis= (Fig. 7) is often found in fresh water adhering to confervæ and other plants of running streams. The protoplasmic body of this animal is enveloped in a chitinous covering that is egg-shaped and of a brownish-yellow color. It is about two millimeters in diameter. When the animal is quiet, no one would suspect its real nature, so much does it look like the seed of an aquatic plant. The testaceous envelope has a single round orifice at its more pointed end. The animal, when in an active state, pushes out the protoplasmic substance, which speedily gives off ramifying extensions, and these by further ramification and inosculation form a complicated network. The protoplasm of the animal also extends itself in such a way as to form a continuous layer on the external surface of the test. From this layer numerous protoplasmic threads may extend out, forming more or less complicated networks. By the alternate contraction and extension of its protoplasmic threads and networks, minute one-celled plants and animals are entrapped like flies in a spider’s web (d). When caught they are carried, by retraction of the protoplasmic thread-like pseudopodia, into the endoplasm in the test. Here the nutritious parts of the entrapped creatures are abstracted and assimilated. In transparent species, the indigestible parts, such as the silicious valves of diatoms, may be distinguished in the midst of the endoplasm, from which they are ultimately extruded.
When gromia oviformis reproduces by mitosis it gives off a bud (small cell), which finally separates from the parent form and constitutes a distinct individual. This process may be repeated many times, so that a great number of separate individuals may be formed, all of which lead detached and independent lives.
Most of the protozoa, which are produced by fission (cell division by mitosis), separate entirely from each other, as in Gromia; but in many of these unicellular animals, the new creatures produced by fission do not separate from one another, but remain more or less closely connected, and thus form _colonies_ of Protozoans. These colonies are of the greatest interest, for they represent a lower stage of the _cell colonies_ of the Metazoa (multicellular animals). They reproduce, in many cases, in a way which is strongly suggestive of reproduction in the Metazoa.
=Microgromia socialis= is a little unicellular animal, having a thin, nearly globular, calcareous shell that it secretes upon its surface. It multiplies by fission, and forms a number of distinct individuals which have the curious habit of fusing their pseudopodia and uniting into a more or less closely associated colony. The individuals sometimes remain at a distance from one another, but sometimes associate themselves together into a compact colony. These individuals are all alike, performing the same functions. There is no division of labor among the units, but they live practically an independent life. If the individual animals were detached from one another, they would live and build new colonies.
=Codosiga umbellata= is another unicellular animal—a flagellate Protozoan. It has a collar-like extension of its ectoplasm from the anterior extremity of its body, forming a sort of funnel from the bottom of which the thread-like structure (flagellum) arises. The vibrations of this flagellum cause a current of the surrounding fluid to set into the funnel so that particles of food reach the soft protoplasmic substance which serves as a mouth. The nucleus is seen near the base of the collar. Near the posterior extremity of the body two contractile vesicles are to be observed. This posterior extremity of the animal has a cylindrical extension of its ectoplasm by which it attaches itself to an object. This protozoan multiplies by longitudinal fission. In some species the animals separate completely from one another and lead entirely independent lives. But in _Codosiga umbellata_ the fission does not extend through the cylindrical extension, so that a group of animals are associated in a colony.
=Rotalia or Globigerina.= The shelled amœba (_Lagena_) gives off a bud (unseparated cell) which grows to the full size, secretes its calcareous shell and remains connected with the parent form. This process may be repeated a number of times until a colony of shelled amœbæ, of varying pattern in different species, may be formed and permanently associated together (Fig. 4). The individual amœbæ are all alike and perform the same functions. There is no division of labor, no specialization, among them. If the individual animals could be separated from one another they would live and build new colonies.
=Pandorina morum= forms a small colony of sixteen cells (solid sphere) of mulberry-like shape and enclosed in a common gelatinous envelope. Each cell in the mulberry mass bears two flagella on its peripheral end. These project out beyond the surface of the gelatinous envelope, and are agents for locomotion of the colony. The cells in the colony are all alike. There is no division of labor among them. They all act alike. The cells (flagellate protozoans) of the colony may reproduce in two ways. Each animal in the colony may subdivide into sixteen smaller units, each of which by growth and multiplication may form a new mulberry mass, a new colony, each unit of which acquires two flagella. Or two of the small units may amalgamate (conjugate), and then develop (by fission) into a new colony. The conjugating units are nearly of the same size and look very much alike.
=Volvox globator= is a spheroidal shaped colony (hollow sphere) of unicellular flagellate animals, about one-half a millimeter in size. It was formerly supposed to be a fresh-water _Alga_. It is now known to be a colony of _Protozoans_. All the animals in this colony are not alike. There is a division of labor among the cells, for some are merely vegetative, serving purposes of nutrition, and having no reproductive powers; while other members of the colony are purely reproductive animals. Furthermore, there is quite a marked specialization of the reproductive cells. Those reproductive cells that may be spoken of as the female cells are large and non-motile encysted cells. The male cells are small and actively motile, in that they have two flagella developed on them. A small flagellate male cell penetrates the large encysted female cell, and as the result of this conjugation, fission takes place repeatedly, and a new colony of flagellate protozoans (volvox) is formed. Volvox approaches very suggestively towards the type of animals known as Metazoan.
In order to comprehend, in some measure, the transition from _Colonial Protozoa_ to _Metazoa_, it will be well for the reader to study a typical sponge. For a long time the Porifera (Sponges) were looked upon as compound Protozoa (colonial Protozoa), but while they are nearer the Protozoa than any of the other types of Metazoa, their position in the animal series is unquestionably among the Metazoa. The Sponge, like the rest of the Metazoa, develops from a fertilized egg by a process of cell multiplication, differentiation, gastrulation, etc.
CELL REPRODUCTION BY MITOSIS.
The multiplication of cells plays a part of such fundamental importance in Evolution, and therefore in Embryology and studies in Heredity, that it is necessary to study the subject somewhat in detail. It is a wonderful process, and is worthy of very careful attention.
[Illustration: FIG. 8.—Diagram illustrating Mitosis. A, the cell commencing activity; B, C, D, phases in the formation of the spindle and the chromatin loops or V’s, also showing that the mother V’s have split into daughter V’s; D, the chromatin loops forming the equatorial plate, _chr_; E, F, G, separation of the daughter loops (daughter chromosomes) and their passage towards the poles of the spindle, thus forming daughter nuclei; H, I, division of the protoplasm so as to form two daughter cells; at, attraction sphere enclosing a centrosome; n m, nuclear membrane; chr., chromatin threads; p, protoplasm; c w, cell wall; sp, spindle.]