2007
DOI: 10.1242/jeb.000307
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Sailing the skies: the improbable aeronautical success of the pterosaurs

Abstract: SUMMARY Pterosaur wings bore a striking resemblance to sails, having a bony spar at the leading edge, formed by the forelimb and one enormously elongated digit,and an elastic wing membrane. Such simple wings would be expected to have performed badly due to excessive deformation, membrane flutter and poor control characteristics. Here I discuss how certain anatomical features,specifically a forewing membrane in the inner part of the wing and a system of fibres embedded in the distal part, may hav… Show more

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Cited by 13 publications
(10 citation statements)
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“…After a long period of debate concerning the role of the hindlimb in pterosaur wing structure, it now appears that evidence strongly supports the inclusion of much or all of the hindlimb in the wing membrane [Unwin and Bakhurina, 1994;Unwin, 1999]. Models of pterosaur aerodynamics [Wilkinson et al, 2006;Wilkinson, 2007] could be readily modified to account for potential effects of active hindlimb positioning and membrane stiffness modulation.…”
Section: Allometric Patterning In the Bat Hindlimbmentioning
confidence: 99%
“…After a long period of debate concerning the role of the hindlimb in pterosaur wing structure, it now appears that evidence strongly supports the inclusion of much or all of the hindlimb in the wing membrane [Unwin and Bakhurina, 1994;Unwin, 1999]. Models of pterosaur aerodynamics [Wilkinson et al, 2006;Wilkinson, 2007] could be readily modified to account for potential effects of active hindlimb positioning and membrane stiffness modulation.…”
Section: Allometric Patterning In the Bat Hindlimbmentioning
confidence: 99%
“…By applying the assumed locomotory muscle forces to a 3D reconstruction of the limb of a tetrapod that is placed in a variety of possible orientations relative to the ground, it will be possible to discover which posture and gait minimises the stresses generated in the bones, with the implication that these reflect the animal's normal mode of locomotion in life. Again, as with dinosaur cranial mechanics, the technique will illuminate the functional significance of transitions to radically new modes of locomotion, for example the origin the bipedality of dinosaurs (Hutchinson 2004), parasagittal gait of mammals (Kemp 1978), and the flight of birds (Garner et al 1999;Clarke et al 2006) and pterosaurs (Wilkinson 2007). …”
Section: Computed Tomography and Finite Element Analysismentioning
confidence: 99%
“…Irrespective of its articulation point, however, debates have centred on whether, or not, the pteroid supported the propatagial region of the pterosaur wing in flight by projecting forward in an anterior orientation (e.g. Hankin 1912;Frey & Riess 1981;Unwin et al 1996;Wilkinson et al 2006;Wilkinson 2007Wilkinson , 2008Unwin 2006) (figure 1a), or was orientated more parallel to the edge of the wing in a medial orientation (e.g. Wagner 1858; Hankin & Watson 1914;Padian 1984;Wellnhofer 1991a;Padian & Rayner 1993;Bennett 2007;Prondvai & Hone 2008) (figure 1b).…”
Section: Introductionmentioning
confidence: 99%
“…Hypotheses for pteroid function have been based on anatomical interpretations of well-preserved fossils (Pennycuick 1988;Unwin et al 1996;Frey et al 2003;Bennett 2007), theoretical consideration of aerodynamic performance advantages (Frey & Riess 1981) and on aerodynamic experiments using models (Wilkinson et al 2006). An anteriorly orientated reconstruction for the pteroid (Wilkinson 2007(Wilkinson , 2008 means that the propatagium must have extended distally from the pteroid to form, in dorsal profile, an elongate triangle to an attachment at the distal end of the wing metacarpal (figure 1c). Proximal to the pteroid, the anterior edge of the propatagium is reconstructed subparallel to the radius/ulna, terminating in the region where the shoulder joins the body (Wilkinson 2007) (figure 1c).…”
Section: Introductionmentioning
confidence: 99%