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http://dx.doi.org/10.5657/fas.2002.5.3.191

Endogenous Rhythm in Oxygen Consumption by the Pacific Oyster Crassostrea gigas (Thunberg)  

Kim Wan-Soo (Marine Environment & Climate Change Laboratory, Korea Ocean Research & Development Institute)
Yoon Seong-Jin (Marine Environment & Climate Change Laboratory, Korea Ocean Research & Development Institute)
Kim Yoon (Marine Environment & Climate Change Laboratory, Korea Ocean Research & Development Institute)
Kim Sung-Yeon (National Fisheries Researches & Development Institute)
Publication Information
Fisheries and Aquatic Sciences / v.5, no.3, 2002 , pp. 191-199 More about this Journal
Abstract
Pacific oysters Crassostrea gigas (Thunberg) were collected on April, 1999 and March­September, 2000 from Goseung Bay along the southern coast of Korea. The oysters tested cp;;ected from a depth of 0.5-2 m in which they cultured by a long line hanging method. The oxygen consumption rates (OCR) of oysters held under constant temperature and darkness (CC), were determined using an automatic intermittent-flow-respirometer (AIFR). Depending on holding periods after oyster collection, the experiments were divided into two groups: Group 7-d (held to ambient temperature for ca. 7 days) and Group 2l-d (held to ambient temperature for ca. 21 days). The OCR for Group 7-d single oyster displayed two peaks every day under CC, while Group 2l-d single oyster showed one peak every day. It is likely that the rhythmic patterns 02.6-12.8 hours) of the OCR in the Group 7-d single oyster may have been influenced by tidal currents at the sampling site. The rhythmic patterns (24.3-24.7 hours) in the Group 2l-d single oyster may have been shifted from two peaks to one peak each day under CC. The present study concludes that the OCR rhythm of wild oysters in nature is governed by two lunar-day clocks (24.8 hours); one driving one peak and the other driving the second peak. When oysters are subjected to the long-term CC conditions, one of the two-clock systems is depressed or only intermittently becomes active. Jpwever. the OCR rhythms by two to three oysters occurred arrhythmic patterns during the experiments and exhibited some evidence of weak rhythmicity of compared to those of a single oyster. It could be partly due to differences group effects.
Keywords
Pacific oyster; Crassostrea gigas; Oxygen consumption; Endogenous rhythm; Circalunidian rhythm;
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1 Webb, H.M. 1976. Interactions of daily and tidal rhythms, In: DeCoursey, D.J. (Ed.) Biological rhythms in the marine environment, University of South Carolina Press, Columbia, pp. 129-135
2 Weiss, R.F. 1970. Thc solubility of nitrogen, oxygen, and argon in water and seawater. Deep Sea Res., 17, 721-735
3 Williams, B G. 1998. The lack of circadian timing in two intertidal invertebrates and its significance in the circatidal/circilunidian debate. Chronobiol. Int., 15, 205-218   DOI   ScienceOn
4 Willson, L.L. and L.E. Burnett. 2000. Whole animal and gill tissue cxygen uptake in the Eastern oyster; Crassostrea virginia: Effects of hypoxia, hypercapnia, air exposure, and in $\`{e}$ction with the protozoan parasite Perkinsus marinas. J. Exp. Mar. Biol, Ecol., 246, 223-240   DOI   ScienceOn
5 Wrona, F.J. and R.W. Davis. 1984. An imporved flow-through respirometer for aquatic macroinvertebrate bioenergetic research. Can. J. Fish. Aquat. Sci., 41, 380-385   DOI
6 Zann, L.P. 1973a. Interactions of the circadian and circatidal rhythms of the littoral gastropod Melanerita atramentosa Reeve. J. Exp. Mar. Biol. Ecol., 11, 249-261   DOI   ScienceOn
7 Zann, L.P. 1973b. Relationships between intertidal zonation and circatidal rhythmicity in littoral gastropods. Mar. Biol, 18, 243-250   DOI
8 Naylor, E. 1976. Rhythmic behaviour and reproduction in marine animals, In: Newell, R.C. (Ed.), Adaptation to environment: essays on the physiology of marine animals, Butterworths, London, pp. 393-429
9 Palmer, J.D. 1997. Duelling hypotheses: Circatidal versus circalunidian battle basics. Chronobiol. Int., 14, 337-346   DOI   ScienceOn
10 Palmer, J.D. 1996. Time, tide and living clocks of marine organisms. Am. Sci., 84, 570-578
11 Palmer, J.D. 1995a. The biological rhythms and clocks of intertidal animals. Oxford University Press, Oxford., pp 1-217
12 Palmer, J.D. 1995b. Review of the dual-clock control of tidal rhythms and the hypothesis that the same clock governs both circatidal and circadian rhythms. Chronobiol. Int., 12, 299-310   DOI
13 Palmer, J.D. and B.G. Williams. 1993. An organic tidal rhythm with a peculiar phenotype. In: Aldrich, J.C. (Ed.), Quantified phenotypic responses in morphology and physiology. Proc. 27th Eur. Mar. Biol. Symp., pp. 121-127
14 Palmer, R.E. 1980. Behavioral and rhythmic aspects of filtration in the bay scallop, Argopecten Irradians concentricus (Say), and the oyster, Crassostrea virginica (Gmelin). J. Exp. Mar. Biol. Ecol, 45, 273-295   DOI   ScienceOn
15 Quayle, D.B. 1988. Pacific oyster culture in British Columbia. Can. Bull. Fish. Aquat. Sci., 218, 1-241
16 Shumway, S.E. 1982. Oxygen consumption in oysters: An overview. Mar. Biol. Letters, 3, 1-23
17 MMAF. 2000. Tide tables (coast of Korea). National Oceanographic Research Institute, Ministry of Maritime Affairs and Fisheries, Republic of Korea, pp. 163-168
18 Shumway, S.E. and R. Koehn. 1982. Oxygen consumption in the American oyster Crassostrea virginica. Mar. Ecol. Prog. Ser., 9, 59-68   DOI
19 Kim, W.S., J.K. Jeon, S.H. Lee and H.T. Huh. 1996. Effects of pentachlorophenol (PCP) on the oxygen consumption rate of the river puffer fish Takifugu obscurus. Mar. Ecol. Prog. Ser., 143, 9-14   DOI   ScienceOn
20 Klapow, L.A. 1972. Natural and artificial rephasing of a tidal rhythm. J. Comp. Physiol., 79, 233-258   DOI
21 Morgan, S.G. 1996. Influence of tidal variation on reproductive timing. J. Exp. Mar. Biol. Ecol., 206, 236-251
22 Morgan, J.D. and G.K. Iwama. 1990. Effects of salinity on growth, metabolism, and ion regulation in juvenile rainbow and Steelhead trout (Oncorhynchus mykiss) and fall Chincook salmon (Oncorhynchus tshawytscha). Can. J. Fish Aquat. Sci., 48, 2083-2094   DOI
23 Morton, B.S. 1977. The tidal rhythm of feeding and digestion in the Pacific oyster, Crassostrea gigas (Thunberg). J. Exp. Mar. Biol. Ecol., 26, 135-151   DOI   ScienceOn
24 Morton, B. 1971. The diurnal rhythm and tidal rhythm of feeding and digestion in Ostrea edulis. Biol. J. Linn. Soc., 3, 329-342   DOI
25 Naylor, E. 1997. Crab clocks re-wounded. Chronobiol. Int., 14, 427-430   DOI   ScienceOn
26 Enright, J.T. 1975. Orientation in time: endogenous clocks. In: Kinne, O. (Ed.), Marine Ecology Vol. II. John Wiley & Sons, London, pp. 917-944
27 Naylor, E. 1996. Crab clockwork: The case for interactive circatidal and circadian oscillators controlling rhythmic locomotor activity of Carcinus maenas. Chronobiol. Int., 13, 153-161   DOI   ScienceOn
28 Bougrier, S., B. Collet, P. Geairon, O. Geffard, M. Heral and J.M. Deslous-Paoli. 1998. Respiratory time activity of the Japanese oyster Crassostrea gigas (Thunberg). J. Exp. Mar. Biol. Ecol., 219, 205-216   DOI   ScienceOn
29 Dowse, H.B. and J.M, Ringo. 1989. The search for hidden periodicities in biological time series revisited. J. Theor. Biol., 139, 487-515   DOI   ScienceOn
30 Higgins, P.J. 1980. Effects of food availability on the valve movements and feeding behavior of juvenile Crassostrea virginica (Gmelin). I. Valve movements and periodic activity. J. Exp. Mar. Biol. Ecol, 45, 229-244   DOI   ScienceOn
31 Kim, W.S., H.T. Huh, J.-G. Je and K.-N. Han. 2002. Evidence of two-clock control of the rhythm of endogenous oxygen consumption in the Washington clam, Saxidomus purpuratus. Mar. Biol. (in press)
32 Kim, W.S., H.T. Huh, S.-H. Huh and T.W. Lee. 2001. Effect of salinity on endogenous rhythm of the Manila clam Ruditapes philippinarum (Bivalvia: Veneridae). Mar. Biol., 138, 157-162   DOI   ScienceOn
33 Kim, W.S., H.T. Huh, J.-H. Lee, H. Rumohr and C.H. Koh. 1999. Endogenous circatidal rhythm in the Manila clam Ruditapes philippinarum (Bivalvia: Veneridae). Mar. Biol., 134, 107-112   DOI   ScienceOn
34 Barnwell, F.H. 1968. The role of rhythmic systems in the adaptation of fiddler crabs to the intertidal zone. Am. Zool., 8, 569-583   DOI
35 Kim, W.S., J.M. Kim, S.K. Yi and H.T. Huh. 1997. Endogenous circadian rhythm in the river puffer fish Takifugu obscurus. Mar. Ecol. Prog. Ser., 153, 293-298   DOI
36 Aldrich, J.C. 1997. Crab clocks sent for recalibration. Chronobiol. Int., 14, 435-437   DOI   ScienceOn
37 Ameyaw-Akumfi, C. and E. Naylor. 1987. Temporal patterns of shell-gape in Mytilus edulis. Mar. Biol., 95, 237-242   DOI
38 Beentjes, M.P. and B.G. Williams. 1986. Endogenous circatidal rhythmicity in the New Zealand cockle Chione stutchburyi (Bivalvia, Veneridae). Mar. Behav. Physiol, 12, 171-180   DOI
39 Bolt, S.R. and E. Naylor. 1985. Interaction of endogenous and exogenous factors controlling locomotor activity rhythms in Carcinus exposed to tidal salinity cycles. J. Exp. Mar. Biol, Ecol., 85, 47-56   DOI   ScienceOn