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Brainerd, E. L.

Publications and source records attributed to Brainerd, E. L..

2 recordsLinked to original sources

Pufferfish inflation: drivers of axial and hoop skin strain and regional variation across the body

Pufferfish skin undergoes large multi-axial extensions during defensive inflation behaviour, as water is pumped into the stomach and the fish increases its body volume threefold. This remarkable capacity for deformation thus raises questions on how skin extension is spatially distributed across the body, and how skin extension relates to changes in body volume and stomach pressure. However, directly measuring skin extension remains experimentally challenging, particularly when attempting to preserve the bodys complex 3D geometry and natural multiaxial strain during ex vivo testing. We used biplanar x-ray videography to measure skin strain (fluoromicrometry) and body volume (dynamic digital endocast) simultaneously with stomach pressure recordings during natural and artificial inflations in porcupinefish ( Diodon holocanthus ). We found no significant difference in maximum body volumes (2.66 {+/-} 0.65 times their initial body volume), body dimensions (e.g., dorsoventral height 87.31 {+/-} 0.23 mm), peak pressures (2.45 {+/-} 1.10 kPa), and skin extension at maximum inflation between natural and artificial inflation conditions. In all inflations, volume increased steadily while stomach pressure only increased during the last 25-50% of inflation. Skin extension varied biaxially, with mean strains reaching up to 102% in the axial direction and 146% in the hoop direction as the fish became nearly spherical. The greatest skin extensions occurred most dorsocranially (axial) and ventrolaterally (hoop). Strains in the hoop direction were only significantly different between body regions (defined as dorsal, lateral and ventral), with the greatest hoop strains occurring in the ventral body region. Our findings may provide insight into existing hypotheses regarding the relationship between volume, pressure, and skin structure and behaviour, while also providing direct in vivo measurements to inform biomimetic design.

zoology↗

Royal knifefish generate powerful suction feeding through large neurocranial elevation and high muscle power output

Suction feeding in ray-finned fishes involves powerful buccal cavity expansion to accelerate water and food into the mouth. Previous XROMM studies in largemouth bass (Micropterus salmoides), bluegill sunfish (Lepomis macrochirus), and channel catfish (Ictalurus punctatus) have shown that more than 90% of suction power in high performance strikes comes from the axial musculature. Thus, the shape of the axial muscles and skeleton may impact suction feeding mechanics. Royal knifefish (Chitala blanci) have an unusual postcranial morphology, with a ventrally flexed vertebral column and relatively large mass of epaxial muscle. Based on their body shape, we hypothesized that royal knifefish would generate high power strikes by utilizing large neurocranial elevation, vertebral column extension, and epaxial shortening. As predicted, C. blanci generated high suction expansion power compared to the other three species studied to date (up to 160 W), which was achieved by increasing both the rate of volume change and the intraoral subambient pressure. The large epaxial muscle (25% of body mass) shortened at high velocities to produce large neurocranial elevation and vertebral extension (up to 41 deg, combined), as well as high muscle mass-specific power (up to 800 W kg-1). For the highest power strikes, axial muscles generated 95% of the power, and 64% of the axial muscle mass consisted of the epaxial muscles. The epaxial-dominated suction expansion of royal knifefish supports our hypothesis that postcranial morphology may be a strong predictor of suction feeding biomechanics. SUMMARY STATEMENTRoyal knifefish rely on their distinct postcranial morphology--with a curved vertebral column and large dorsal body muscles--to produce large neurocranial elevation and powerful suction feeding.

zoology↗