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Re: Paedomorphosis ( Re: BARYONYX' CLAWS )
<< I wish you'd stop calling "swimming" flying. It doesn't help your
argument a bit. These are birds that have exapted their flight anatomy
for the purpose of swimming through water. In becoming more efficient
swimmers, they lost the ability to fly through the air. You noted in a
previous post that there may have been a transitional stage in which the
wings were used both for flying through the air and swimming through the
water. With this I can agree. Likewise with small, arboreal theropods,
there was probably a stage in which the forelimbs were used for grasping
and climbing and for some kind of flying. In later theropods, the
grasping uses prevailed; in later birds, the flying uses prevailed. Why
is this incredibly simple, obvious, and natural idea so difficult for
you to accept?>>
I'm not calling swimming flying. Just because cetaceans swim does
not mean they fly. However, where the swimming birds differ from
cetaceans, swimming birds had volant ancestors and their wings still
take on a function that is similiar to the flight stroke so they are not
"flightless" in the sense of ratites. They still are essentially fiers.
This incredibly simple, obvious, and natural idea is so hard for me to
accept because the submarine fliers still use their forelimbs for the
same functions as flight ( creating thrust, moving the body ). In your
transitional pseudo-phylogeny the small arboreal climbing/gliders would
not use their forelimbs for the same functions as flight ( creating
thrust, etc ). The majority of the work would have to be done with the
hindlimbs. And while this is happening, paedomorphosis would have to
occur for the animal to become completely flightless and the forelimbs
to be freed from their flight motions. And since there is no evidence of
the paedomorphic trends seen in flightless birds in theropods, this
scenario is unlikely.
<<All you're saying here is that theropods would have made lousy
swimmers (if they tried to use their forelimbs for this). With this, I
would probably agree, too.>>
No. Retaining volant characteristics in penguins, auks, and
plotopterids is essential for their type of swimming or flight. Now, if
in theropods, they needed to use their forelimbs for predation : why
wouldn't they lose flight the typical avian way ( paedomorphosis ) and
tweak their forelimbs to work the way it does in phorusrhacids ? ( in
which flight was lost the typical avian way and the forelimbs was
modified ).
>>The basic theropod shoulder girdle is utterly different from the
>>penguin, auk, and plotopterids. And the penguin, auk, and
>>plotopterids still use the same basic flying motions.
<<Of course the basic theropod shoulder girdle is different. The avian
shoulder girdle had not yet evolved when "basic theropods" (whatever
those are) diverged. The "basic theropod" ancestor probably used its
wings for grasping as well as for some kind of flying (certainly not
powered, flapping flight, but perhaps a kind of fluttering--better than
nothing for those moments of free fall when living in the trees).>>
Grasping is not an adaptation that comes easily from the avian
flight apparatus. It goes against the basic movements of the avian
forelimb. In phorusrhacids the forelimb has been remodeled and changed
so the flight apparatus can be made into a grasping organ. Nothing of
the sort was done in theropods, whose forelimbs were of conversative
design. Lets look at the avian flight apparatus ( this would apply for
"primitive" fliers too ) :
The avian flight apparatus has two main muscles, the M pectoralis (
downstroke ) and the M. supracoracoideus ( upstroke and humeral rotation
). Plus the M. biceps branchii ( pulling limb forward ) and the dorsal
elevators ( pulling the humerus back ). Now flight is impossible, even
for primitive fliers, without lift, thrust, and special forelimb
mechanics. For the wing to be exapted for grasping the M. biceps
branchii would have to be hypertrophied ( because the motions of
grasping are basically where the limb is pulled forward ) and the M.
pectoralis and M. supracoracoideus would have to either atrophy or
change their function to work with the M. biceps branchii. Since this
features are not seen in theropods ( features along these lines are seen
in penguins because thrust is the main component of their flight ) it is
unlikely that they came from flying ancestors.
>You're making me ramble.
Rambling is good. It makes people think.
MattTroutman
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