But it may be questioned, on obvious probability grounds, whether
this way of accounting for the observed absence of intermediates
will really wash. Admitting that every intermediate stage "must
have" a small population, we may nevertheless observe that there
must have been a far greater number of them than of the stable, "
finished" species known to us, since (according to the Darwinist
picture) every species-transition must necessarily pass through
several intermediate stages. That greater number would increase
the likelihood that some intermediate forms, here and there, would
chance to be preserved as fossils. And the dogma further requires
that the larger transitions - between different genera, families,
orders, classes, and even different phyla, must all have come about
in just the same gradual and continuous manner, simply by a long-
continued succession of normal species-transitions! We have all
seen "genealogical trees" drawn by evolutionists, to show the
order in which these taxonomic groups have all come into existence
over a long period, by successive "branchings from a common root".
But it must be asked: Where are all the fossils that should have
been left by the many millions of species that this tree requires
to have once existed on its trunk, boughs, and branches, before
its final branchings took place? Why are none of these seen in
the fossil record of the period during which the evolutionists'
tree requires them to have lived? (That this perhaps surprising
charge does not exaggerate the real situation will be seen under
"First Taxonomic Disconfirmation", where the explicitly contra-
Darwinian testimony of the "transformed cladists" will be
presented.)
Moreover, why have none of this great multitude of Darwinian intermediate
species chanced to survive unchanged to our own time, among the
considerable number of ancient life-forms that, as we know, have
had the luck to do so? You may perhaps have read that that actually
ts the case: the lungfishes, the monotremes (platypus) and the
hoatzin, among others, were at one time said to show us "living
fossils" of "primitive" life at a stage that was still intermediate
to two different later forms, and ancestral to both of them. But
those claims are no longer heard; for, on closer investigation,
all of these creatures turned out to be curious "mosaic" constructions
of a kind that could not rationally be seen as representing the
real historical transitions between one group and another. (See
Denton's book for a detailed exposition of these cases.) The recent
discovery' of that living fossil par excellence, the coelacanth,
was an exciting event for evolutionists, because these "lobe-finned"
fish were supposed to have already begun to "evolve toward amphi-
bians"; but when a well-preserved specimen was obtained, examination
of its fins and its internal organs (previously unknown and only
guessed-at) quashed that fond hope for some real confirmation
of Darwin's ideas, and I think that you will no longer find coelacanths
called "pre-amphibians".....
......The most recent episode of great changes, the advent of the modern
(Cenozoic) mammals after the death of the dinosaurs, is the one
that we should expect to have left the best-preserved fossils
of intermediate species. At the catastrophic end of the Cretaceous,
65 Myr ago, mammals were small nocturnal "tree-shrew"-like animals,
none larger than cats; roughly ten million years later, we find
essentially "modern" bats*, bears, and lions18. "All modern orders
of mammals seem to have arisen independently and at about the
same time": Wesson, p. 40, quoting Bonner 1988 and Carroll 1988.
If these vast changes really proceeded in the manner prescribed
by Darwin, surely many hundreds (at the least!) of intermediate
species in each lineage must once have lived during that protracted
period of radical transmogrification. None of them have ever showed
up in the fossil record.
And not only are all traces
of intermediate species' missing, but anyone who seriously tries
to imagine a believable sequence of viable intermediate animals
between a tree-shrew and a bat-every one of which, according to
Darwin, supplanted its predecessor by virtue of being "better
adapted"! -wiII very soon be convinced that such a sequence is
simply inconceivable: "What use is half a wing?" as everyone since
Mivart (including even Gould) has asked. The reason we have found
no trace of them is simply that they never existed, and the reason
they never existed is that it would be impossible for them to
have done so. It was this unavoidable conclusion that led Simpson
in 1944 20 to publicly acknowledge his heretical conviction that
these megaevolutionary" transformations, at least, must have
occurred in some rapid and entirely non-Darwinian way. For this
he was censured, and forced to recant, but it is safe to assert
that no one has ever been able to sketch out, with even the slightest
semblance of credibility, any Darwinian route to the already-"
modern" bats that appear-twice over! in the early Cenozoic, roughly
55 million years ago.
There are in fact two distinct suborders of bats, the Microchiroptera
and Megachiroptera, so pervasively different in structure that
everyone agrees that they must have "evolved" quite
independenty: Wesson, p.i82.