Data from: Pulmonary anatomy and a case of unilateral aplasia in a common snapping turtle (Chelydra serpentina): developmental perspectives on cryptodiran lungs
The common snapping turtle (Chelydra serpentina) is a well studied and broadly distributed member of Testudines; however, very little is known concerning developmental anomalies and soft tissue pathologies of turtles and other reptiles. Here, we present an unusual case of unilateral pulmonary aplasi...
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Zusammenfassung: | The common snapping turtle (Chelydra serpentina) is a well studied and
broadly distributed member of Testudines; however, very little is known
concerning developmental anomalies and soft tissue pathologies of turtles
and other reptiles. Here, we present an unusual case of unilateral
pulmonary aplasia, asymmetrical carapacial kyphosis, and mild scoliosis in
a live adult C. serpentina. The detailed three-dimensional (3D) anatomy of
the respiratory system in both the pathological and normal adult C.
serpentina, and a hatchling are visualized using computed tomography (CT),
microCT, and 3D digital anatomical models. In the pathological turtle, the
right lung consists of an extrapulmonary bronchus that terminates in a
blind stump with no lung present. The left lung is hyperinflated relative
to the normal adult, occupying the extra coelomic space facilitated by the
unusual mid-carapacial kyphotic bulge. The bronchial tree of the left lung
retains the overall bauplan of the normal specimens, with some minor
downstream variation in the number of secondary airways. The primary
difference between the internal pulmonary structure of the pathological
individual and that of a normal adult is a marked increase in the surface
area and density of the parenchymal tissue originating from the secondary
airways, a 14.3% increase in the surface area to volume ratio. Despite
this, the aplasia has not had an impact upon the ability of the turtle to
survive; however, it did interfere with aquatic locomotion and buoyancy
control under water. This turtle represents a striking example of a
non-fatal congenital defect and compensatory visceral hypertrophy. |
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DOI: | 10.5061/dryad.160mp |