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Influence of temperature on the larval development of the edible crab, Cancer pagurus

Published online by Cambridge University Press:  20 January 2009

Monika Weiss ,
Sven Thatje ,
Olaf Heilmayer ,
Klaus Anger ,
Thomas Brey  and
Martina Keller
Monika Weiss
Affiliation:
Alfred-Wegener-Institut für Polar-und Meeresforschung, Am Handelshafen 12, 27570 Bremerhaven, Germany
Sven Thatje*
Affiliation:
National Oceanography Centre, Southampton, School of Ocean and Earth Science, University of Southampton, European Way, SO14 3ZH Southampton, United Kingdom
Olaf Heilmayer
Affiliation:
Alfred-Wegener-Institut für Polar-und Meeresforschung, Am Handelshafen 12, 27570 Bremerhaven, Germany National Oceanography Centre, Southampton, School of Ocean and Earth Science, University of Southampton, European Way, SO14 3ZH Southampton, United Kingdom
Klaus Anger
Affiliation:
Biologische Anstalt Helgoland, Stiftung Alfred-Wegener-Institut für Polar- und Meeresforschung, 27498 Helgoland, Germany
Thomas Brey
Affiliation:
Alfred-Wegener-Institut für Polar-und Meeresforschung, Am Handelshafen 12, 27570 Bremerhaven, Germany
Martina Keller
Affiliation:
Alfred-Wegener-Institut für Polar-und Meeresforschung, Am Handelshafen 12, 27570 Bremerhaven, Germany
*
Correspondence should be addressed to: S. Thatje, National Oceanography Centre, Southampton, School of Ocean and Earth Science, University of Southampton, European Way, SO14 3ZH Southampton, United Kingdom email: [email protected]
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Abstract

The influence of temperature on larval survival and development was studied in the edible crab, Cancer pagurus, from a population off the island of Helgoland, North Sea. In rearing experiments conducted at six different temperatures (6°, 10°, 14°, 15°, 18° and 24°C), zoeal development was only completed at 14° and 15°C. Instar duration of the Zoea I was negatively correlated with temperature. A model relating larval body mass to temperature and developmental time suggests that successful larval development is possible within a narrow temperature range (14° ± 3°C) only. This temperature optimum coincides with the highest citrate synthase activity found at 14°C. A comparison for intraspecific variability among freshly hatched zoeae from different females (CW 13–17 cm, N = 8) revealed that both body mass and elemental composition varied significantly. Initial larval dry weight ranged from 12.1 to 17.9 μg/individual, the carbon content from 4.6 to 5.8 μg/individual, nitrogen from 1.1 to 1.3 μg/individual, and the C:N ratio from 4.1 to 4.4. A narrow larval temperature tolerance range of C. pagurus as well as the indication of intraspecific variability in female energy allocation into eggs may indicate a potential vulnerability of this species to climate change. Large-scale studies on the ecological and physiological resilience potential of this commercially fished predator are needed.

Keywords

Brachyuraearly ontogenyedible crabelemental composition
Type
Research Article
Information
Journal of the Marine Biological Association of the United Kingdom , Volume 89 , Issue 4 , June 2009 , pp. 753 - 759
Copyright
Copyright © Marine Biological Association of the United Kingdom 2009

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References

REFERENCES

Anger, K. (2001) The biology of decapod crustacean larvae. Lisse: A.A. Balkema Publishers, Crustacean Issues 14, 420 pp.Google Scholar
Anger, K. and Dawirs, R.R. (1982) Elemental composition (C, N, H) and energy in growing and starving larvae of Hyas araneus (Decapoda, Majidae). Fisheries Bulletin 80, 419–433.Google Scholar
Anger, K., Lovrich, G.A., Thatje, S. and Calcagno, J.A. (2004) Larval and early juvenile development of Lithodes santolla (Molina, 1782) (Decapoda: Anomura: Lithodidae) reared at different temperatures in the laboratory. Journal of Experimental Marine Biology and Ecology 306, 217–230.CrossRefGoogle Scholar
Bernardo, J. (1996) The particular maternal effect of propagule size, especially egg size: patterns, models, quality of evidence and interpretations. American Zoologist 36, 216–236.CrossRefGoogle Scholar
Birkeland, C. and Dayton, P.K. (2005) The importance in fishery management of leaving the big ones. Trends in Ecology and Evolution 20, 356–358.CrossRefGoogle ScholarPubMed
Bradford, M.M. (1976) A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein–dye binding. Analytical Biochemistry 72, 248–254.CrossRefGoogle ScholarPubMed
Dahlhoff, E.P. (2004) Biochemical indicators of stress and metabolism: applications for marine ecological studies. Annual Review of Physiology 66, 183–207.CrossRefGoogle ScholarPubMed
Dawirs, R.R. (1979) Effects of temperature and salinity on larval development of Pagurus bernhardus (Decapoda, Paguridae). Marine Ecology Progress Series 1, 323–329.CrossRefGoogle Scholar
Dawirs, R.R. (1985) Temperature and larval development of Carcinus maenas (Decapoda) in the laboratory: prediction of larval dynamics in the sea. Marine Ecology Progress Series 24, 297–302.CrossRefGoogle Scholar
Dawirs, R.R. and Dietrich, A. (1986) Temperature and laboratory feeding rates in Carcinus maenas L. (Decapoda: Portunidae) larvae from hatching through metamorphosis. Journal of Experimental Marine Biology and Ecology 99, 133–147.CrossRefGoogle Scholar
DeMartini, E.E., DiNardo, G.T. and Williams, H.A. (2003) Temporal changes in population density, fecundity, and egg size of the Hawaiian spiny lobster (Panulirus marginatus) at Necker Bank, Northwestern Hawaiian Islands. Fisheries Bulletin 101, 22–31.Google Scholar
Fischer, S. and Thatje, S. (2008) Temperature-induced oviposition in the brachyuran crab Cancer setosus along a latitudinal cline: aquaria experiments and analysis of field data. Journal of Experimental Marine Biology and Ecology 357, 157–164.CrossRefGoogle Scholar
Gardner, C. (1997) Effect of size on reproductive output of giant crabs Pseudocarcinus gigas (Lamarck): Oziidae. Marine and Freshwater Research 48, 581–587.CrossRefGoogle Scholar
Giménez, L. and Anger, K. (2003) Larval performance in an estuarine crab, Chasmagnathus granulata, is a consequence of both larval and embryonic experience. Marine Ecology Progress Series 249, 251–264.CrossRefGoogle Scholar
Giménez, L. and Torres, G. (2002) Larval growth in the estuarine crab Chasmagnathus granulata: the importance of salinity experienced during embryonic development, and the initial larval biomass. Marine Biology 141, 877–885.CrossRefGoogle Scholar
Giménez, L., Anger, K. and Torres, G. (2004) Linking life history traits in successive phases of a complex life cycle: effects of larval biomass on early juvenile development in an estuarine crab, Chasmagnathus granulata. Oikos 104, 570–580.CrossRefGoogle Scholar
Harms, J., Anger, K., Klaus, S. and Seeger, B. (1991) Nutritional effects on ingestion rate, digestive enzyme activity, growth, and biochemical composition of Hyas araneus L. (Decapoda: Majidae) larvae. Journal of Experimental Marine Biology and Ecology 145, 233–265.CrossRefGoogle Scholar
Hastie, T.J. and Tibshirani, R.J. (1990) Generalized Additive Models. London: Chapman & Hall/CRC Press, 335 pp.Google Scholar
Heilmayer, O., Brey, T. and Pörtner, H.O. (2004) Growth efficiency and temperature in scallops: a comparative analysis of species adapted to different temperatures. Functional Ecology 18, 641–647.CrossRefGoogle Scholar
Heilmayer, O., Thatje, S., McClelland, C., Conlan, K. and Brey, T. (2008) Changes in biomass and elemental composition during early ontogeny of the Antarctic isopod crustacean Ceratoserolis trilobitoides. Polar Biology 31, 1325–1331.CrossRefGoogle Scholar
Ingle, R.W. (1981) The larval and post-larval development of the edible crab, Cancer pagurus Linnaeus (Decapoda: Brachyura). Bulletin of the British Musuem of Natural History (Zoology) 40, 211–236.Google Scholar
Kaiser, R. and Gottschalk, G. (1972) Ausreissertest nach Nalimov. Elementare Tests zur Beurteilung von Messadaten. Mannheim, Wien, Zürich: Bibliographisches Institut, pp. 18–21.Google Scholar
Krimsky, L.S. and Epifanio, C.E. (2008) Multiple cues from multiple habitats: effect on metamorphosis of the Florida stone crab, Menippe mercenaria. Journal of Experimental Marine Biology and Ecology 358, 178–184.CrossRefGoogle Scholar
Lannig, G., Eckerle, L.G., Serendero, I., Sartoris, F.J., Fischer, T., Knust, R., Johansen, T. and Pörtner, H.O. (2003) Temperature adaptation in eurythermal cod (Gadus morhua): a comparison of mitochondrial enzyme capacities in boreal and Arctic populations. Marine Biology 142, 589–599.CrossRefGoogle Scholar
Lemos, D., Salomon, M., Gomes, V., Phan, V.N. and Buchholz, F. (2003) Citrate synthase and pyruvate kinase activity during early life stages of the shrimp Farfantepenaeus paulensis (Crustacea, Decapoda, Penaeidae): effects of development and temperature. Comparative Biochemistry and Physiology B 135, 707–719.CrossRefGoogle ScholarPubMed
Lovrich, G.A., Thatje, S., Calcagno, J.A., Anger, K. and Kaffenberger, A. (2003) Changes in biomass and chemical composition during lecithotrophic larval development of the southern king crab, Lithodes santolla (Molina). Journal of Experimental Marine Biology and Ecology 288, 65–79.CrossRefGoogle Scholar
Marshall, D.J. and Keough, M.J. (2004) When the going gets rough: effect of maternal size manipulation on larval quality. Marine Ecology Progress Series 272, 301–305.CrossRefGoogle Scholar
Neal, K.J. and Wilson, E. (2004) Cancer-pagurus. Edible crab. Marine Life Information. Network: Biology and Sensitivity Key Information Sub-programme (online). Plymouth: Marine Biological Association of the United Kingdom.Google Scholar
Pörtner, H.O. (2001) Climate change and temperature-dependent biogeography: oxygen limitation of thermal tolerance in animals. Naturwissenschaften 88, 137–146.Google ScholarPubMed
Pörtner, H.O., Berdal, B., Blust, R., Brix, O., Colosimo, A., Wachter, B., Giuliani, A., Johansen, T., Fischer, T., Knust, R., Lannig, G., Naevdal, G., Nedenes, A., Nyhammer, G., Sartoris, F.J., Serendero, I., Sirabella, P., Thorkildsen, S. and Zakhartsev, M. (2001) Climate induced temperature effects on growth performance, fecundity and recruitment in marine fish: developing a hypothesis for cause and effect relationships in Atlantic cod (Gadus morhua) and common eelpout (Zoarces viviparus). Continental Shelf Research 21, 1975–1997.CrossRefGoogle Scholar
Pörtner, H.O., Storch, D. and Heilmayer, O. (2005) Constraints and trade-offs in climate dependent adaptation: energy budgets and growth in a latitudinal cline. Scientia Marina 69, 39–55.CrossRefGoogle Scholar
Ouellet, P. and Plante, F. (2004) An investigation of the sources of variability in American lobster (Homarus americanus) eggs and larvae: female size and reproductive status, and interannual and interpopulation comparisons. Journal of Crustacean Biology 24, 481–495.CrossRefGoogle Scholar
Reznick, D. (1981) ‘Grandfather effects’: the genetics of interpopulation differences in offspring size in the Mosquito Fish. Evolution 35, 941–953.Google ScholarPubMed
Salomon, M. and Buchholz, F. (2000) Effects of temperature on the respiration rates and the kinetics of citrate synthase in two species of Idotea (Isopoda, Crustacea). Comparative Biochemistry and Physiology 125, 71–81.CrossRefGoogle ScholarPubMed
Sidell, B.D., Driedzic, W.R., Stowe, D.B. and Johnston, I.A. (1987) Biochemical correlations of power development and metabolic fuel preferenda in fish hearts. Physiological Zoology 60, 221–232.CrossRefGoogle Scholar
Sokal, R.R. and Rohlf, F.J. (1981) Biometry—the principles and practice of statistics in biological research. San Francisco: W.H. Freeman, 859 pp.Google Scholar
Somero, G.N. (2005) Linking biogeography to physiology: evolutionary and acclimatory adjustments of thermal limits. Frontiers in Zoology 2.CrossRefGoogle ScholarPubMed
Thatje, S., Anger, K., Calcagno, J.A., Lovrich, G.A., Pörtner, H.O. and Arntz, W.E. (2005) Challenging the cold: crabs reconquer the Antarctic. Ecology 86, 619–625.CrossRefGoogle Scholar
Torres, C.G. and Escribano, R. (2003) Growth and development of Calanus chilensis nauplii reared under laboratory conditions: testing the effects of temperature and food resources. Journal of Experimental Marine Biology and Ecology 294, 81–99.CrossRefGoogle Scholar
Wells, R.M.G., Lu, J., Hickey, A.J.R. and Jeffs, A.G. (2001) Ontogenetic changes in enzyme activities associated with energy expenditure during development in the spiny lobster, Jasus edwardsii. Comparative Biochemistry and Physiology 130, 339–347.CrossRefGoogle ScholarPubMed
Wiltshire, K.H. and Manly, B.F.J. (2004) The warming trend at Helgoland Roads, North Sea: phytoplankton response. Helgoland Marine Research 58, 269–273.CrossRefGoogle Scholar
Woll, A.K., van der Meeren, G.I. and Fossen, I. (2006) Spatial variation in abundance and catch composition of Cancer pagurus in Norwegian waters: biological reasoning and implications for assessment. ICES Journal of Marine Science 63, 421–433.CrossRefGoogle Scholar