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Re: Epidexipteryx feathers
(Posted in plain text.)
____
Listers,
Without speculating on the possible functional role of the elongate tail
feathers on _Epidexipteryx_, they are inherently interesting. The authors
describe the distal portions of the 'non-ETF" (that is, the body feathers
rather than the tail feathers) as "composed of filamentous parallel
barbs, similar to the condition seen in the non-shafted feathers..." Well
a "non-shafted" feather is usually referred to a down, so there is
probably no reason to introduce a new term here. The parallel
configuration could result from the fact that each was produced
independently and they were preserved in registrar, or they share a
common base, which not was preserved and the barbs ended up preserved in
a comb-like registration. The authors observe that the "free distal barbs
arise from the edge of a membranous structure, an arrangement that has
never been previously reported". This is not quite accurate. In many
tipped feather structures, for example Cedar Waxwings (Brush & Allen,
1963); Scaled Cuckoo (Brush, 1965) and others (Brush, 1967) the barbs are
fused to form a scale-like structure. These structures are always distal
ward on the feather and in some cases individual barbs protrude. the
structure is produced by the fusion of barbs along the selected portion
of the feather and are produced by the follicle as the feather is
produced (this means it begins early in development and then switches to
a standard shaft/barb pattern). The facial shield on the Purple Gallinule
and American Coot appear to be similarly constructed. I suspect, but
obviously cannot proved that the feathers on Epidexipteryx are produced
by a similar mechanism.
The long ribbon-like tail feathers may also have a precedence. In their
chapter on Birds in the "The Jehol Fossils" Zhang and Zhou describe two
such cases. One in the well known _Confuciusornis_ of a pair of elongate
tail feathers which have a racquet-like structure. Similar feathers exist
in extant Motmots and hummingbirds. The mechanism by which they are
produced is known and they are considered to be involved in display. The
second is in the same chapter in the reconstruction of _Protopteryx_ they
indicate the long "central tail feather...may represent the ancestral
type of feather" (pg 144). The implication is that a scale was somehow
reconfigured into a feather. A similar scenario for the origin of
feathers was proposed by P. Regal (1975). This scenario is unlikely as
avian scales develop differently and contain different from extant
reptilian scales. The statement itself disagrees with Zhang and Zhou's
description (pg 123) of the 'current picture of feather evolution" which
is essentially that proposed by Prum & Brush (2002, 2003).
It seems unnecessary to coin new terms to describe the feathers on
_Epidexipteryx_. All the features occur in extant feathers and are
produced by a common mechanism based on the geometry and ontological
processes of the follicle. Fusion of parts (barbs, barbules, etc) not
uncommon is a variety of taxa implying that it is a mechanism capable of
producing a great deal of morphological variety. Apparently these very
early forms were no exception.
Alan H Brush
brushes2@juno.com
92 High Street
Mystic, CT. 06355
(860) 572-1717
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