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Re: bauplan convergence
Neither display nor insulation provides a >primary cause< for the
evolution of feathers. When an organism has no feathers, it cannot use
them for display, for brooding, or for insulation(!). This would require
the organism to predict the future (e.g., "I will need insulation and to
show off, so I'll evolve feathers"). Rather, the first feathers evolved
for some other reason, and as soon as or very shortly after they
appeared, they would have found secondary uses (exaptations) for display
or for insulation (or for parachuting). But the primary cause must have
been something positive and internal. The best suggestion I've read so
far is that feathers appeared as a means of sulfur excretion through
molting. Excess sulfur is used up in the
keratin proteins of the feathers, which are shed from time to time during
the animal's life. The excess sulfur itself may have resulted from a
metabolic shift toward homeothermy in the archosaur lineage.<<<<
I've always been fond of the excess sulfur speculation on the origin of
feathers, although (or is that "because" ;-) it's largely untestable for the
forseeable future. Here's an equally plausible scenario:
Endothermic dinosaur species X has a hard time sheding excess heat in
its warm Mesozoic locale. One individual has elongate scales, which
increases surface area, enhancing cooling behaviors such as sitting in the
shade. It doesn't (much)increase the surface area visible to the sun, so
there is little negative impact on thermodynamics even when dinosaur X is
forced into the midday sun. As the scales continue to elongate, the surface
area for cooling increases, further benifiting our dinosaurs descendants.
(Note that I'm not refering to long spatulate scales as is often pictured in
discussions of feather evolution, but rather thin conical ones that would
develop from elongating roundish pebbled dinosaur skin, rending the annimal
with a bristly appearance not un similar to the proto feathered critter
Luis Rey painted for your "Birds Came First" article in Omni) Further
elongagation of these scales would continue to provide cooling benifits to
descendants, until the scales started to overlap and trap air beneath them,
at which point they could start to serve as insulation. Everyone thinks of
insulation as keeping animals warm, but it was hot in the Mesozoic, and
small animals are more prone to overheating than large animals. A small,
tropical, endothermic dinosaur would have benefitted greatly from protection
against the sun (if only because it would have increased midday foraging
time during the summer), after which its descendants could have exapted it
for use in cooler climates, to look sexy, to fly with, etc.
I admit I'm more or less pulling this out of thin air here, but th idea
does generate testable predictions (i.e. future fossil finds), and there is
an interesting bit of speculation I can pull from feather ontogeny that may
be wonderfully consistent with it. During development, the feather is
encased in a keratinous sheath that is filled with a blood supplied pulp
cavity. As the feather further develops, the pulp cavity leaves behind a
series of division in the calamus (quill) called pulp caps. Of course,
these are filled with air. I mention this because a blood filled epidermal
structure would do a superb job of cooling an animal in the shade, while a
hollow tip would protect the blood supply from direct sunlight, while
simulaneously pre-adapting the structure for insulation once an air layer
could be trapped underneath the pellage.
Just somethin' to think about.
Scott
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