Abstract
The escape swimming performance of the Antarctic scallop, Adamussium colbecki, was measured in animals acclimated for 6 weeks to −1, 0 or 2°C and tested at −1.5 to +1.5°C. Clap duration and swimming velocity were significantly related to temperature, but were not affected by acclimation, demonstrating no phenotypic plasticity. Comparisons of the mean swimming velocity of A. colbecki with the published data for temperate and tropical species showed little evidence for evolutionary compensation for temperature, with all data fitting to a single exponential relationship with a Q10 of 2.08 (0–20°C). The contraction kinetics of the isolated fast adductor muscle of A. colbecki were determined and the times to 50% peak tension and 50% relaxation had Q10s (0–4°C) of 3.6 and 4.7, respectively. The Q10 of the overall relationship for pooled time to peak twitch data for four scallop species was 2.05 (0–20°C). Field studies revealed low mobility and poor escape performance in wild A. colbecki. A combination of thermodynamic constraints, reduced food supply, and lower selective pressure probably explains the low levels of swimming performance seen in A. colbecki.
Similar content being viewed by others
References
Ansell AD, Cattaneo-Vietti R, Chiantore M (1998) Swimming in the Antarctic scallop Adamussium colbecki: analysis of in situ video recordings. Antarct Sci 10:369–375
Bailey DM (2001) The thermal dependence of swimming and muscle physiology in temperate and Antarctic scallops. PhD Thesis, University of St. Andrews
Bailey DM, Johnston IA (in press) Scallop swimming kinematics and muscle performance: modelling the effects of “within-animal” variation in temperature sensitivity. Mar Fresh Behav Physiol
Bailey DM, Peck LS, Bock C, Pörtner HO (2003) High-energy phosphate metabolism during exercise and recovery in temperate and Antarctic scallops—an in vivo 31P-NMR study. Physiol Biochem Zool 76:622–633
Barbeau MA, Scheibling RE (1994a) Procedural effects of prey tethering experiments—predation of juvenile scallops by crabs and seastars. Mar Ecol Prog Ser 111:305–310
Barbeau MA, Scheibling RE (1994b) Temperature effects on predation of juvenile sea scallops (Placopecten magellanicus (Gmelin)) by sea stars (Asterias vulgaris Verill) and crabs (Cancer irroratus Say). J Exp Mar Biol Ecol 182:27–47
Barbeau MA, Scheibling RE (1994c) Behavioural mechanisms of prey size selection by sea stars (Asterias rubens Verrill) and crabs (Cancer irroratus Say) preying on juvenile sea scallops (Placopecten magellanicus (Gmelin)). J Exp Mar Biol Ecol 180:103–136
Barbeau MA, Scheibling RE, Hatcher BG (1998) Behavioural responses of predatory crabs and sea stars to varying density of juvenile sea scallops. Aquaculture 169:87–98
Beamish FWH (1978) Swimming capacity. In: Hoar WS, Randall DJ (eds) Fish physiology. Academic, New York, pp 101–187
Berkman PA (1988) Ecology of the circumpolar Antarctic Scallop, Adamussium colbecki (Smith, 1902). PhD Thesis, University of Rhode Island
Berkman PA (1990) The population biology of the Antarctic Scallop, Adamussium colbecki (Smith 1902) at New Harbor, Ross Sea. In: Kerry KR, Hempel G (eds) Antarctic ecosystems ecological change and conservation. Springer, Berlin Heidelberg New York, pp 281–288
Bologna PAX, Heck KL (1999) Differential predation and growth rates of bay scallops within a seagrass habitat. J Exp Mar Biol Ecol 239:299–314
Brey T, Clarke A (1993) Population dynamics of marine benthic invertebrates in antarctic and subantarctic environments: are there unique adaptations? Antarct Sci 5:253–266
Cheng J-Y, Demont ME (1996) Jet-propelled swimming in scallops: swimming mechanics and ontogenic scaling. Can J Zool 74:1734–1748
Cheng J-Y, Davison IG, Demont ME (1996) Dynamics and energetics of scallop locomotion. J Exp Biol 199:1931–1946
Frederich M, Sartoris FJ, Pörtner HO (2001) Distribution patterns of decapod crustaceans in polar areas: a result of magnesium regulation? Polar Biol 24:719–723
Hardewig I, Van Dijk PL, Pörtner HO (1998) High-energy turnover at low temperatures: recovery from exhaustive exercise in Antarctic and temperate eelpouts. Am J Physiol 274:R1789–R1796
Hardewig I, van Dijk PL, Moyes CD, Pörtner HO (1999) Temperature-dependent expression of cytochrome-c oxidase in Antarctic and temperate fish. Am J Physiol 277:R508–R516
Hatcher BG, Scheibling RE, Barbeau MA, Hennigar AW, Taylor LH, Windust AJ (1996) Dispersion and mortality of a population of sea scallop (Placopecten magellanicus) seeded in a Tidal Channel. Can J Fish Aquat Sci 53:38–54
Heilmayer O, Brey T (2003) Saving by freezing? metabolic rates of Adamussium colbecki in a latitudinal context. Mar Biol 143:477–484
James RS, Cole NJ, Davies MLF, Johnston IA (1998) Scaling of intrinsic contractile properties and myofibrillar protein composition of fast muscle in the fish Myoxocephalus scorpius L. J Exp Biol 201:901–912
Johnston IA, Altringham JD (1985) Evolutionary adaptation of muscle power output to environmental temperature: force-velocity characteristics of skinned fibres isolated from antarctic, temperate and tropical marine fish. Eur J Physiol 405:136–140
Johnston IA, Walesby NJ, Davison W, Goldspink G (1975) Temperature adaptation in myosin of Antarctic fish. Nature 254:74–75
Johnston I, Calvo J, Guderley YH (1998) Latitudinal variation in the abundance and oxidative capacities of muscle mitochondria in perciform fishes. J Exp Biol 201:1–12
Manuel JL, Dadswell MJ (1990) Swimming behaviour of juvenile giant scallop, Placopecten magellanicus, in relation to size and temperature. Can J Zool 69:2250–2254
Marsh RL, Olson JM, Guzik SK (1992) Mechanical performance of scallop adductor muscle during swimming. Nature 357:411–413
Morton B (1980) Swimming in Amusium pleuronectes (Bivalvia: Pectinidae). J Zool (Lond) 190:375–404
Olson JM, Marsh RL (1993) Contractile properties of the striated adductor muscle in the bay scallop Argopecten irradians at several temperatures. J Exp Biol 176:175–193
O’Steen S, Cullum AJ, Bennett AF (2002) Rapid evolution of escape performance in Trinidadian guppies (Poecilia reticulata). Evolution 56:776–784
Peck LS, Webb KE, Bailey DM (2004) Extreme sensitivity of biological function to temperature in Antarctic marine species. Funct Ecol 18:625–630
Smith EA (1902) VII. Mollusca. In: Report on the collection of natural history made in the Antarctic regions during the voyage of the Southern Cross. British Museum (NH), London, pp 201–213
Thatje S, Arntz WE (2004) Antarctic reptant decapods: more than a myth? Polar Biol 27:195–201
Thorburn IW, Gruffydd LD (1979) Studies of the behaviour of the scallop Chlamys opercularis (L) and its shell in flowing sea water. J Mar Biol Assoc UK 59
Wakeling JM, Johnston IA (1998) Muscle power output limits fast-start performance in fish. J Exp Biol 201:1505–1526
Watkins TB (1995) Predator-mediated selection on burst swimming performance in tadpoles of the Pacific tree frog, Pseudacris regilla. Physiol Zool 69:154–167
Wilbur AE, Gaffney PM (1997) A genetic basis for geographic variation in shell morphology in the bay scallop, Argopecten irradians. Mar Biol 128:97–105
Wilson RS, Franklin CE, Davison W, Kraft P (2001) Stenotherms at sub-zero temperatures: thermal dependence of swimming performance in Antarctic fish. J Comp Phys B 171:263–269
Acknowledgements
The excellent support by the personnel at Rothera and in the Fish Muscle Research Group in St. Andrews is gratefully acknowledged. D.M.B. was supported by a NERC Cooperative Awards in Sciences of the Environment studentship supervised by L.S.P. and I.A.J.
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Bailey, D.M., Johnston, I.A. & Peck, L.S. Invertebrate muscle performance at high latitude: swimming activity in the Antarctic scallop, Adamussium colbecki. Polar Biol 28, 464–469 (2005). https://doi.org/10.1007/s00300-004-0699-9
Received:
Revised:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00300-004-0699-9


