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Re: Testing competitive exclusion in birds, bats and pterosaurs
Mike, I wish I were as articulate as you.... :-)
Cloud streets define repeating boundary layer roll vortices, and are a
wonderful source of energy for traveling. Temperature and pressure changes
along those vortices cause the clouds that make them visible. Using them
and microlift, Gary Osoba has set a number of world's distance records in
small sailplanes with size and performance characteristics very similar to
the larger pterosaurs. Non-stop flights of several hundred miles are quite
feasible for these aircraft and for the larger pterosaurs (if appropriately
configured).
In fact, it is even possible to remain aloft all day and to travel with
nothing available but spots of strong SINK. Vertical wind shear is very
effective as a source of energy for soaring, and horizontal shear is not far
behind. You can extract energy anytime the air is pushing you in the
direction you are going, whether that be up, down, or sideways. To stay up
using sink, you need to be flying fairly fast with wings approximately level
and push over downward as you enter the sink (experiencing reduced g loads).
You want the downward moving air to push you downward so that you
accelerate. The sink area needs to be small in horizontal extent so that
you won't overspeed. Then as you exit the far side of the sink, you rapidly
pull up at more than 1g, thereby converting the kinetic energy you gained
back to the potential energy of altitude. You can also use the same
technique along the boundary of any atmospheric 'edge' where shear is
present. You can replace the downward sink with a transient overbank, a
bank greater than 90 degrees, sliding back and forth across the 'edge' to
extract energy from it. This works great, though it makes for a bumpy ride
and vigorous maneuvering. There is one caveat. It needs a fairly high
wingloading and a high aspect ratio. For example, an Anhanguera piscator
with a narrow wing planform scales up consistently in increased weight, wing
loading, and aspect ratio from the wandering albatross, implying the ability
to uses similar sources of atmospheric energy (which include those described
above). The broadwing version of Anhanguera piscator is not so appropriate.
JimC
----- Original Message -----
From: "Michael Habib" <mhabib5@jhmi.edu>
To: <dinosaur@usc.edu>
Sent: Monday, May 07, 2007 10:53 PM
Subject: Re: Testing competitive exclusion in birds, bats and pterosaurs
In addition, the planforms proposed for wings connected to the hindlimb in
pterosaurs tend to be poor even for a terrestrial soaring form, with both
the estimated loadings and aspect ratios often falling well below those
seen in living dedicated thermal soarers. Living raptors and storks do
not have wings nearly as short and broad (nor masses as low) as some
individuals seem to expect. After all, living inland soaring birds use a
number of sources of lift other than thermals, many of which are better
extracted with greater spans and/or higher loadings. Such species also
have to travel between lifting sources at a reasonable rate. Not to
mention that the largest pterodactyloids would be seriously pushing the
limit with regards to being able to stay within a narrow thermal ring,
simply by virtue of total span. Cloud streets would be much more useful
to an animal that size, and I expect that extracting energy from cloud
streets would usually select for a narrow chord planform.
Cheers,
--Mike H.