It seems that in most cases the spermatozoa swim around at random and
that their union with the eggs is assured only by their enormous number;
only in a few cases in plants have there been discovered special stimuli
of a chemical nature, which attract the spermia to the egg.
But we cannot enter here more fully into the physiology of
fertilisation, and shall only remark that its real significance is by no
means clear.[6]
[6] The older theories, attributing to fertilisation (or to
“conjugation,” *i.e.* its equivalent in Protozoa), some sort of
“renovation” or “rejuvenescence” of the race, have been almost
completely given up. (See Calkins, *Arch. für Entwickelungsmechanik*,
xv. 1902). R. Hertwig recently has advocated the view, that abnormal
relations between the amounts of nuclear and of protoplasmatic material
are rectified in some way by those processes. Teleologically, sexual
reproduction has been considered as a means of variability (Weismann),
but also as a means of preserving the type!
THE FIRST DEVELOPMENT PROCESS OF ECHINUS
Turning now definitively to the special kind of organism, chosen of our
type, the common sea-urchin, we properly begin with a few words about
the absolute size of its eggs and spermatozoa. All of you are familiar
with the eggs of birds and possibly of frogs; these are abnormally
large eggs, on account of the very high amount of reserve material they
contain. The almost spherical egg of our Echinus only measures about a
tenth of a millimetre in diameter; and the head of the spermatozoon has
a volume which is only the four-hundred-thousandth part of the volume
of the egg! The egg is about on the extreme limit of what can be seen
without optical instruments; it is visible as a small white point. But
the number of eggs produced by a single female is enormous and may
amount to hundreds of thousands; this is one of the properties which
render the eggs of Echinus so very suitable for experimental research;
you can obtain them whenever and in any quantity you like; and,
moreover, they happen to be very clear and transparent, even in later
stages, and to bear all kinds of operations well.
The spermia enters the egg, and it does so in the open water--another
of the experimental advantages of our type. Only one spermia enters
the egg in normal cases, and only its head goes in, the tail is left
outside. The moment that the head has penetrated the protoplasm of the
egg a thin membrane is formed by the latter. This membrane is very soft
at first, becoming much stronger later on; it is very important for all
experimental work, that by shaking the egg in the first minutes of its
existence the membrane can easily be destroyed without any damage to the
egg itself.
Public-domain text, read in full here on John Shaqi.
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