Measurements were made of the surface areas (As) of the skin and gills of larval and juvenile walleye Stizostedion vitreum with a body mass (M) of between 2 mg (1 day post hatch) and 2.3 g (98 days post hatch). The skin, with a relative surface area (As/M) of approximately 8500 mm2 g−1, accounted for more than 99.9 % of the total surface area (skin + gills) at 1 day post hatch. The relative area of the skin decreased as fish grew at an allometric rate of b−1=−0.32±0.01 (mean ± S.E.M., where b−1 is the specific-mass exponent in the allometric equation Y×M−;1=aMb−;1, in which Y is surface area and a is a constant). The relative surface area of the gills (filaments + lamellae) increased in a hyperbolic fashion from very low levels (approximately 5 mm2 g−1) at 1 day post hatch to reach a maximum of approximately 1100 mm2 g−1 at a body mass of approximately 200 mg. Thereafter, relative gill area declined at an allometric rate of b−;1=−;0.19±0.10 (mean ± S.E.M.). Gill area, because it declined at a slower relative rate, finally exceeded skin area at a body mass of approximately 700 mg. The relative surface area of the skin and gills combined (total surface area) decreased at a more- or-less constant allometric rate of b−;1=−;0.21±0.01 (mean ± S.E.M.) throughout the experimental period. On the basis of the allometric rates of expansion, the structural capacity to supply oxygen (b−;1=−;0.19; total gill area, this study) and metabolic demand for oxygen (b−;1≈−;0.13; mean literature value for routine and resting metabolism) appear to remain fairly closely matched in postlarval walleye (>300 mg). The two parameters do not display the same degree of concordance during larval development. In larvae, total respiratory surface area declines on a mass-specific basis at roughly the same rate (b−;1=−;0.21) as gill area does in older fish but, unlike in older fish, metabolic demand for oxygen does not change (b−;1≈0.0). This results in a progr. essive decline in effective respiratory surface area (As/MO2) but does not affect O2 uptake, probably because larvae are so small that surface area is not the limiting factor in gas exchange. Analysis of data from the literature suggests that surface area typically becomes limiting at a body mass of approximately 100 mg. The major function of gills in smaller larvae (<100 mg) appears to involve ionoregulation or related aspects of acid–base balance rather than respiratory gas exchange.

You do not currently have access to this content.