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Swimming has evolved in only a few orders of Bivalves. In this study, the behavior, morphometry, and mechanics of swimming in the file shell Limaria fragilis were characterized and compared to the better understood scallops. Absolute swimming speed (cm sec À1 ) increased with increasing shell height, although relative swimming speed (body lengths sec À1 ) did not covary with shell height. The increase in absolute swimming speed was due to an increase in the distance covered during each valve clap as clap distance (cm clap À1 ) also increased with shell height while clapping frequency (claps sec À1 ) did not covary with animal size. Limaria fragilis displayed a variety of morphological changes related to size. Shell length was negatively allometric with shell height indicating the shell became proportionately slimmer in larger animals. Dry shell mass was negatively allometric with shell height, while both dry adductor muscle mass and dry mantle þ tentacle mass were positively allometric. Autotomy of mantle tentacles significantly decreased clap distance by 13% without affecting clapping frequency or swimming speed.

SUMMARY We investigated divalent cation and anaerobic end-product concentrations and the interactive effects of these substances and pH on haemocyanin oxygen-binding (Hc-O2) in the New Zealand abalone Haliotis iris. During 24 h of environmental hypoxia (emersion), d-lactate and tauropine accumulated in the foot and shell adductor muscles and in the haemolymph of the aorta, the pedal sinus and adductor muscle lacunae, whereas l-lactate was not detected. Intramuscular and haemolymph d-lactate concentrations were similar, but tauropine accumulated to much higher levels in muscle tissues. Repeated disturbance and short-term exposure to air over 3 h induced no accumulation of d- or l-lactate and no change in [Ca2+], [Mg2+], pH and O2-binding properties of the native haemolymph. The haemolymph showed a low Hc-O2 affinity, a large reverse Bohr effect and marked cooperativity. Dialysis increased Hc-O2 affinity, obliterated cooperativity and decreased the pH-sensitivity of O2 binding. Replacing Mg2+ and Ca2+ restored the native O2-binding properties and the reverse Bohr shift. l- and d-lactate exerted minor modulatory effects on O2-affinity. At in vivo concentrations of Mg2+ and Ca2+, the cooperativity is dependent largely on Mg2+, which modulates the O2 association equilibrium constants of both the high-affinity (KR) and the low-affinity (KT) states (increasing and decreasing, respectively). This allosteric mechanism contrasts with that encountered in other haemocyanins and haemoglobins. The functional properties of H. iris haemocyanin suggest that high rates of O2 delivery to the tissues are not a priority but are consistent with the provision of a large O2 reserve for facultatively anaerobic tissues during internal hypoxia associated with clamping to the substratum.

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