At the end of the first full paragraph on p. 703, Lauder and colleagues point out that closely related species can differ for two very different reasons. What are these two causes of species differences? I'm confused about what those two reasons are as I can't find the reasons.
Transcribed Image Text: outlines as well as discrete land- being based increasingly on phylo-
marks, and traditional multivariate genetic information. The diversity
of organismal function (and its rela-
tended to deal more effectively with tionship to structure) is a vast area
of unexplored biology. With the in-
shape. In particular, the traditional fusion of historical methods and
concepts from systematics, the fu-
ture promises exciting advances as
not possible with a one- or two-
taxon study.
In many other comparative stud-. statistical methods have been ex-
ies the explicit intent is to address
evolutionary issues such as physi- such biological problems as size and
ological adaptation to an extreme
environment. For such studies, the
choice of species for analysis can be
guided by systematic information domain, with the benefit that many physiologists and morphologists
(Burggren 1991, Garland et al. 1991,
Huey 1987). A comparison of close
relatives reduces, for instance, the
probability that observed differences
between taxa are an artifact of long-
separate phylogenetic history rather statistical tools for the study of
than of adaptation to a particular morphology has had on research on
environmental feature.
bivariate approach to allometry has
been extended into the multivariate
studies of form today, whatever their bring new tools to bear on the analy-
purpose, are multivariate in nature.
It would be difficult to overesti-
mate the impact that the develop-
ment of both data acquisition and
sis of structural and functional di-
versity.
Acknowledgments
We gratefully acknowledge the con-
tributions of the many members of
the last decade has the promise of the original two committees (espe-
cially T. Garland) for Systematics
Agenda 2000 (Quantitative and Evo-
organismal form; in truth, only in
Detecting evolutionary anachro- Thompson's approach to structure
nisms. A systematic and historical
perspective also is useful in detect- study the deformation of one shape lutionary Morphology, Comparative
ing evolutionary anachronisms (i.e.,
traits that evolved in response to largely qualitative and inaccurate
conditions no longer existing). For
example, the giant fruits of some
Neotropical trees might have evolved
as adaptations for dispersal by Pleis-
tocene megafauna (Janzen and Mar- analytical methods used to study ously supported by the National
tin 1982), and the presence of flight form, there is no doubt that the
motor neurons (currently nonfunc-
tional) in flightless crickets probably metrics and phylogenetics has manuscript was supported by: NSF
reflects the evolution of flightless grass- opened up a broad array of new
hoppers from ancestors that could fly questions. It has also raised the stan-
(Dumont and Robertson 1986).
Thus, an appreciation of phylo- (Zelditch et al. 1992, 1995).
genetic history sometimes clarifies
the function-or the lack thereof-
of an otherwise puzzling physiologi-
cal trait (Huey 1987). A phyloge- Physiological and functional traits
netic analysis may reveal that the
traits thought to represent novel evo-
lutionary responses to current envi-
ronments may have been retained sity recognition and preservation has
from an ancestral condition that had
little in common with current envi-
ronmental conditions.
been realized. Early attempts to
into another, for example, were
Physiology and Biochemistry) who
assisted in the preparation of the
and not readily amenable to statisti- original reports that formed the ba-
sis of this article. This article is a
product of the initiative Systemat-
ics Agenda 2000, which was gener-
cal study.
Although vigorous debate con-
tinues on the assumptions of the
Science Foundation through grant
recent rapprochement of morpho- DEB-9396035. Preparation of the
IBN-9119502 to George Lauder,
NSF DEB-9301151 to Ray Huey,
and NSF BSR-8604960 and BSR-
8911433 to Russell Monson.
dards to which answers will be held
Conclusions
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November 1995
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