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Colin Patterson Revisits His Famous Question about Evolution
Origins & Design 17:1
A Colin Patterson Sampler
1977: "The Contribution of Paleontology
to Teleostean Phylogeny," in Major Patterns of
Vertebrate Evolution, eds. M.K. Hecht, P.C. Goody, and B.M.
Hecht (New York: Plenum Press, 1977), pp. 579-643.
A major, well-illustrated paper in Patterson's specialty, the
systematics of fishes, which shows his developing skepticism about
the value of evolutionary theory in systematics. Patterson compares
the practices of pre-Darwinians, e.g., Agassiz, with post-Darwinians:
Where Agassiz refrained from linking the converging bases
of his lineages (Fig. 1) since he
believed that their junction 'may only be sought in the creative
intelligence,' the theory of evolution allows a modern author
to represent a hypothetical ancestral group as having the same
reality as any other major taxon. Yet the search for ancestors
of the teleosts has hardly been successful, for every other major
branch point in Figure 18 is also occupied by hypothetical forms
or question-marks: these ancestors have no more reality than
the abstract synapomorphy-bearers indicated by the open circles
in Figure 17.
1979: Interview with Luther D. Sunderland,
June 30,British Museum of Natural History, ERIC Document
Reproduction Service microfiche ED 228 056 (available at most
public libraries), pp.7-19.
Sunderland, late creationist activist (d. 1987), interviewed
several paleontologists while preparing his book Darwin's Enigma.
This interview is marked by a fair amount of miscommunication,
but also by passages such as the following:
Sunderland: ...How do you see that evolution might explain
the origin of fishes?
Patterson: (Pause)
Sunderland: Then you'd rather not say?
Patterson:Ten years ago I'd have been perfectly willing to
tell you, but it so happens that I know someone who is working
this problem for about 15 years--the starfish end of it--the
echinoderms. He believes that this development could be traced
from the Cambrian with the echinoderms. I could very easily refer
you to his work and say that I agree with him that fish are related
to echinoderms, but I do not think it is obvious.
1980: "Cladistics,"
The Biologist 27: 234-240.
A popular article, drafted as the "transformed cladistics"
controversy was growing to its height. "As the theory of
cladistics has developed," argued Patterson (p. 239), "it
has been realized that more and more of the evolutionary framework
is inessential, and may be dropped. The chief symptom of this
change is the significance attached to nodes in cladistics. In
Hennig's book, as in all early works in cladistics, the nodes
are taken to represent ancestral species. This assumption has
been found to be unnecessary, even misleading, and may be dropped."
"Phylogenies and Fossils,"
Systematic Zoology 29: 216-219.
More skepticism about fossils and phylogeny: "To me, one
of the most astonishing consequences of the furor over cladistics
is the realization that the current account of tetrapod evolution,
shown in a thousand diagrams and everywhere acknowledged as the
centerpiece of historical biology, is a will-o'-the-wisp. For
nowhere can one find a clear statement of how and why the Recent
groups are interrelated, and the textbook stories are replete
with phantoms--extinct, uncharacterizable groups giving rise one
to another" (p. 217).
1981: "Significance of Fossils
in Determining Evolutionary Relationships," Annual
Review of Ecology and Systematics 12: 195-223.
Patterson's classic, critical analysis of the role of fossils
in systematics: "...extinct paraphyletic groups [common in
neo-Darwinian phylogenies before the cladistic revolution] seem
to me to obscure rather than illuminate relationships, for they
exist not in nature but in the minds of evolutionists. Such groups
lead to a sterile inversion of problems of relationships, which
come to depend not on comparative analysis of what is accessible--the
Recent biota--but on juggling with what is inaccessible--uncharacterizable
abstractions from the fossil record" (p. 219).
1982: "Morphological Characters
and Homology," in Problems of Phylogenetic Reconstruction,
eds. K.A. Joysey and A.E. Friday, Systematics Association Special
Vol. No. 21 (New York: Academic Press), pp. 21-74.
Perhaps the most widely-cited paper on homology of the past
two decades, where Patterson discusses five ways of defining homology
(classical, evolutionary, phenetic, cladistic, and utilitarian),
taking issue with "the evolutionists...for here I do expect
disagreement" (p. 62). Patterson's main complaint is with
extinct, paraphyletic groups, which typically play the role of
"transitional forms" in evolutionary reasoning. "Such
groups," Patterson argued, "...are imagined by evolutionists,
those most committed to the confirmation of Darwin's views. The
power of this mystery, extinct paraphyletic groups as the source
of phylogeny, is shown by the fact that we still have no cladogram,
or series of nested homologies, for tetrapods, the group in which
phylogeny is supposed to be best known" (p. 64).
1983: "How does phylogeny differ
from ontogeny?" in Development and Evolution,
eds. B.C. Goodwin, N. Holder and C. Wylie (Cambridge: Cambridge
Univ. Press), pp. 1-31.
A discussion of the bearing of ontogenetic (developmental)
data on phylogeny: "Phylogeny is generalised transformation,
but we have no empirical experience of phylogeny; the only transformations
of which we have empirical evidence are those of ontogeny"
(p. 21).
1988: "Homology in Classical and
Molecular Biology," Molecular Biology and Evolution
5: 603-625.
Patterson applies his 1982 analysis of homology (see above)
to molecular data. This paper is notable for its claim that, at
the molecular level (unlike gross morphology), "there is
no detected molecular equivalent of convergence--or of misleading
similarity--except in the most trivial sense" (p. 618).
1993: "Congruence Between Molecular
and Morphological Phylogenies," Annual Review of
Ecology and Systematics 24: 153-188.
In a review written with fellow British Museum staffers David
Williams and Christopher Humphries, Patterson surveys the congruence
-- or lack thereof -- between molecular and morphological phylogenies.
He and his co-authors conclude:
As morphologists with high hopes of molecular systematics,
we end this survey with our hopes dampened. Congruence between
molecular phylogenies is as elusive as it is in morphology and
as it is between molecules and morphology....Partly because of
morphology's long history, congruence between morphological phylogenies
is the exception rather than the rule. With molecular phylogenies,
all generated within the last couple of decades, the situation
is little better. Many cases of incongruence between molecular
phylogenies are documented above; and when a consensus of all
trees within 1% of the shortest in a parsimony analysis is published...structure
or resolution tends to evaporate (p. 180).
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Copyright © 1996 Paul Nelson. All rights
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File Date: 6.22.96
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