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COMPOSITION OF THE HUMAN OVUM -i^jj<br />
and altered ovum is in a condition to assume the cleavage necessary to the formation of the blastodermic membrane,<br />
which in the higher vertebrates is the starting-point for the embryo and foetus. The changes which supervene during<br />
the fertilising process bear a certain analogy to those occurring in the foetus itself (Plate xcii., Fig. 1, E, F, G, H, I,<br />
page 396), so that the scheme of reproduction is, from the first, involved and complex, and the outcome of pre-<br />
arrangement and design.<br />
While the matrices of the two pronuclei appear to blend, their chromatin filaments maintain their identity.<br />
The chromatin filaments form two sets of looped-v-shaped fibres of two each, and as these ultimately divide<br />
longitudinally they make two sets of four each. At one stage they flatten and arrange themselves transversely<br />
across the ovum, and so participate in, if they do not actually cause, the division of the ovum into two. They<br />
subsequently open out transversely, and then at right angles, and in conjunction with radiating, concentric, ovoid,<br />
and circular arrangements in the attraction-spheres complete the division of the ovum.<br />
The several points discussed in connection with the maturation, discharge, and fertiUsation of the ovum are<br />
illustrated at Plate xc, Plate xci., and Plate xcii.. Fig. 1, pp. 391, 393, and 396.<br />
§ 72. Parts Entering into the Composition of the Human Ovum.<br />
The human ovum in its entirety consists of the following parts : (1) globular zona pelluoida, otherwise called<br />
zona radiata ; (2) globular vitelline membrane ; (3) globular vitellus or yolk, consisting of protoplasm and nutritive<br />
material ; (4) globular germinal vesicle containing globular germinal spot.<br />
The same parts are encountered in the rabbit.<br />
The several parts of the ovum can only be made out by the aid of the microscope. In Plate Ixxxvi., page 383,<br />
A, the ovum is seen under pressure and is more or less flattened. In B, C, the zona pellucida or radiata,<br />
which has considerable resisting power, is purposely burst ; the protoplasm and nutritive material forming the<br />
vitellus or yolk (6), and the germinal vesicle (c) having escaped. At D, the radiation in the zona pellucida (now<br />
known as zona radiata) is indicated (a), as also the vitellus (6), germinal vesicle (c), and germinal spot {3,). The radiation<br />
of the zona pellucida is beheved to contain pores, which permit the passage of noirrishment to the ovum and<br />
provide entrances to the spermatozoa. The zona pellucida on leaving the Graafian foUicle is invested with a clear,<br />
granular substance resembling the white of egg, which is supposed to contribute to the nourishment of the ovum, and<br />
disappears when the ovum reaches the Fallopian tube. The protoplasm of the ovum on a casual examination is a<br />
clear, apparently structureless, substance. On a closer examination, and when re-agents are employed, it is seen<br />
to consist of a fine reticulum especially observable near the periphery of the ovum and around the germinal vesicle :<br />
in other words, the protoplasm is differentiated. The other ingredients of the ovum (deutoplasm) contribute to<br />
its nourishment.<br />
The germinal spot, which measures -^^ to yj„ of an inch in diameter, consists of a nuclear membrane<br />
containing a clear material, with strands of karyoplasm enclosing one or more nucleoli. If only one nucleolus occurs<br />
it is known as the germinative spot {macula germinativa) . A certain amount of differentiation is also traceable<br />
in the germinal vesicle. The old idea, that protoplasm is identical and structureless, may now be regarded as<br />
exploded. The amount of nutritive material suppUed to the ovum is less in mammals than in fishes, reptiles, and<br />
birds, and Professor F. M. Balfour conveniently divided ova into those with (a) accumulation of nutritive or<br />
yolk matter at one pole (telolecithal ova—fish, reptile, and bird among vertebrates) ; (b) those with the accumulation<br />
of yolk in the middle ovum {centrolecithal ova— ^in arthropods) ; and (c) those with yolk scattered equally and<br />
in small amount through the protoplasm of the ovum {alecithal—mammals, amphioxus, echinoderms). This<br />
distribution of the nutritive material (proto- and deuto-plasm) determines to a large extent the nature of the<br />
segmentation in the several ova.<br />
The development of the ovum after it leaves the ovary is at once intrinsic and extrinsic : intrinsic as regards<br />
changes occurring in itself, and extrinsic as regards changes induced in it by the presence of the spermatozoon or<br />
male element.<br />
The intrinsic changes consist in the extrusion of certain constituents of the nucleus of the ovum known as the<br />
" polar globules " : the extrinsic changes consisting in the intrusion into the nucleus of a spermatozoon or sperm-<br />
cell to take the place of the extruded polar globules. The ovum or female element on its part makes room for the<br />
spermatozoon or male element, and the latter takes full advantage of the arrangement. The male and female<br />
elements come together, and either fuse and merge into each other's substance or, as B. v. Beneden thinks, they<br />
maintain their identity, and mutually produce a double or compound cell, which is the starting-point of the new<br />
being (Plate Ixxxvi., H to S inclusive, page 383).<br />
The fertilisation of the ovum, it will be seen, is brought about by a union of the most intimate kind ;<br />
the male<br />
3 B