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The effect of temperature on brood duration in three Halicarcinus species (Crustacea: Brachyura: Hymenosomatidae)

Published online by Cambridge University Press:  31 August 2011

Anneke M. van den Brink ,
Colin. L. McLay ,
Andrew M. Hosie  and
Michael J. Dunnington
Anneke M. van den Brink*
Affiliation:
IMARES, part of Wageningen UR, Korringaweg 5, Yerseke 4401 NT, The Netherlands
Colin. L. McLay
Affiliation:
School of Biological Sciences, Canterbury University, PB 4800, Christchurch, New Zealand
Andrew M. Hosie
Affiliation:
Western Australian Museum, 49 Kew Street, Perth 6106, Australia
Michael J. Dunnington
Affiliation:
School of Biological Sciences, Canterbury University, PB 4800, Christchurch, New Zealand
*
Correspondence should be addressed to: A.M. van den Brink, IMARES, part of Wageningen UR, Korringaweg 5, Yerseke 4401 NT, The Netherlands email: [email protected]
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Abstract

The effect of temperature on brood development was investigated for three intertidal hymenosomatid crabs: Halicarcinus cookii, H. varius and H. innominatus in Kaikoura, New Zealand. The duration of brood incubation decreased as temperature increased, as did the interbrood period. The duration of each stage of brood development also decreased with increased temperature, but the proportion of total incubation time for each stage remained relatively similar at different temperatures. Hymenosomatid crabs have determinate growth, but moult to maturity at different sizes, thereafter devoting most of their energy to reproduction. The number of broods a female could carry in her lifetime was estimated for each species. Halicarcinus cookii was estimated to be able to produce eight complete broods of 1146 eggs per lifetime, H. varius was estimated to be able to produce seven complete broods of 1051 eggs per lifetime and H. innominatus was estimated to be able to produce six complete broods of 1081 eggs per life time. With the predicted global temperature rise of 2°C in the next 50 years, the authors estimate that, for all three species, a female could produce one extra brood per lifetime (a 10–15% increase in fecundity depending on species), even more if crabs reach maturity faster, potentially leading to a significant population increase.

Keywords

incubation durationegg developmenttemperature effectbrood stagefecunditydeterminate growthHymenosomatidaeHalicarcinusinterbroodclimate changeKaikouraNew Zealand
Type
Research Article
Information
Journal of the Marine Biological Association of the United Kingdom , Volume 92 , Issue 3 , May 2012 , pp. 515 - 520
Copyright
Copyright © Marine Biological Association of the United Kingdom 2011

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References

REFERENCES

Ali, M.H., Salman, S.D. and Aladhub, A.Y. (1995) Population dynamics of the hymenosomatid crab Elamenopsis kempi in a brackish subtidal region of Basra, Iraq. Scientia Marina 59, 1–13.Google Scholar
Anger, K. (1983) Temperature and the larval development of Hyas araneus L. (Decapoda: Majidae); extrapolation of laboratory data to field conditions. Journal of Experimental Marine Biology and Ecology 69, 203–215.CrossRefGoogle Scholar
Anger, K., Thatje, S., Lourich, G.A. and Calcagno, J.A. (2003) Larval and early juvenile development of Paralomis granulosa reared at different temperatures: tolerance of cold and food limitation in a litlodid crab from high latitudes. Marine Ecology Progress Series 253, 243–251.CrossRefGoogle Scholar
Brockerhoff, A.M. and McLay, C.L. (2005) Mating behaviour, female receptivity and male–male competition in the intertidal crab Hemigrapsus sexdentatus (Brachyura: Grapsidae). Marine Ecology Progress Series 290, 179–191.CrossRefGoogle Scholar
Brockerhoff, A.M. and McLay, C.L. (2011) Human-mediated spread of alien crabs. In Galil, B.S., Clark, P.F. and Carlton, J.T. (eds) In the wrong place: alien marine crustaceans—distribution, biology and impacts, invading nature. Springer Series in Invasion Ecology 6. Dordrecht, Heidelberg, London and New York: Springer, pp. 27–106.CrossRefGoogle Scholar
Dunnington, M.J. (1999) The reproductive strategies of the pill-box crab Halicarcinus innominatus Richardson, 1949. MSc thesis. University of Canterbury, Christchurch, New Zealand.Google Scholar
Hartnoll, R.G. (1969) Mating in the Brachyura. Crustaceana 16, 161–181.CrossRefGoogle Scholar
Hartnoll, R.G. (1985) Growth, sexual maturity and reproductive output. In Wenner, A.M. (ed.) Factors in adult growth. Rotterdam: A.A. Balkema, pp. 101–128.Google Scholar
Hines, A.H. (1982) Allometric constraints and variables of reproductive effort in brachyuran crabs. Marine Biology 69, 309–320.CrossRefGoogle Scholar
Hoegh-Guldberg, O., Mumby, P.J., Hooten, A.J., Steneck, R.S., Greenfield, P., Gomez, E., Harvell, C.D., Sale, P.F., Edwards, A.J., Caldeira, K., Knowlton, N., Eakin, C.M., Iglesais-Prieto, R., Muthiga, N., Bradbury, R.H., Dubi, A. and Hatziolos, M.E. (2007) Coral reefs under rapid climate change and ocean acidification. Science 318, 1737–1742.CrossRefGoogle ScholarPubMed
Hosie, A. (2004) The reproductive ecology of Halicarcinus varius (Brachyura: Hymenosomatidae) Dana, 1851. MSc thesis. University of Canterbury, Christchurch.Google Scholar
Jansen, K.P. (1971) Ecological studies on intertidal Sphaeromatidae (Isopoda: Flabellifera). Marine Biology 11, 262–285.CrossRefGoogle Scholar
Leffler, C.W. (1972) Effects of temperature on the growth and metabolic rate of juvenile blue crabs, Callinectes sapidus, in the laboratory. Marine Biology 14, 104–110.CrossRefGoogle Scholar
Lucas, J.S. (1980) Spider crabs of the family Hymenosomatidae (Crustacea, Brachyura) with particular reference to Australian species: systematics and biology. Records of the Australian Museum 33, 148–247.CrossRefGoogle Scholar
Lucas, J.S. and Hodgkin, E.P. (1970) Growth and reproduction of Halicarcinus australis (Haswell) (Crustacea, Brachyura) in the Swan Estuary, Western Australia II. Larval stages. Australian Journal of Marine and Freshwater Research 20, 163–173.CrossRefGoogle Scholar
McLay, C.L. and Van den Brink, A.M. (2009) Relative growth and size at sexual maturity in Halicarcinus cookii (Brachyura: Hymenosomatidae): why are some crabs precocious maters? Journal of the Marine Biological Association of the United Kingdom 89, 743–752.CrossRefGoogle Scholar
Melrose, M.J. (1975) The marine fauna of New Zealand: family Hymenosomatidae (Crustacea, Decapoda, Brachyura). Wellington: New Zealand Department of Scientific and Industrial Research.Google Scholar
Nakanishi, T. (1981) The effect of temperature on growth, survival and oxygen consumption of larvae and post-larvae of Paralithodes brevipes (Decapoda: Anomura). Bulletin of the Japanese Sea Region Fisheries Research Laboratory 32, 49–56.Google Scholar
Okamoto, K. (1993) Influence of temperature on survival and growth of larvae of the giant spider crab Macrocheira kaempferi (Crustacea, Decapoda, Majidae). Bulletin of the Japanese Sea Region Fisheries Research Laboratory 32, 49–56.Google Scholar
Richer de Forges, B. (1977) Étude du crabe des lles Kerguelen: Halicarcinus planatus (Fabricius). In Comité National Français des Recherches Antarctiques, Paris, pp. 71–133.Google Scholar
Shields, J.D. (1991) The reproductive ecology and fecundity of Cancer crabs. In Wenner, A.M. and Kuris, A. (eds) Crustacean egg production. Rotterdam: A.A. Balkema, pp. 193–213.Google Scholar
Stillman, J.H. (2002) Causes and consequences of thermal tolerance limits in rocky intertidal Porcelain crabs, genus Petrolisthes. Integrative and Comparative Biology 42, 790–796.CrossRefGoogle ScholarPubMed
Van den Brink, A. M. (2006) The reproductive ecology and biology of the pillbox crab: Halicarcinus cookii (Brachyura: Hymenosomatidae) Filhol, 1885. MSc thesis. University of Canterbury, New Zealand.Google Scholar
Van den Brink, A.M. and McLay, C.L. (2009) Use of sterile male technique to investigate sperm competition, storage and use in a pill box crab, Halicarcinus cookii (Brachyura: Hymenosomatidae). Journal of Crustacean Biology 29, 62–69.CrossRefGoogle Scholar
Van den Brink, A.M. and McLay, C.L. (2010) Competing for last place: mating behaviour in a pill box crab, Halicarcinus cookii (Brachyura: Hymenosomatidae). Zoologischer Anzeiger 249, 21–32.CrossRefGoogle Scholar
Vinuesa, J.H., Ferrari, L. and Lombardo, R.J. (1985) Effect of temperature and salinity on larval development of southern king crab (Lithodes antarcticus). Marine Biology 85, 83–87.CrossRefGoogle Scholar
Walther, K., Anger, K. and Pörtner, H.O. (2010) Effects of ocean acidification and warming on the larval development of the spider crab Hyas araneus from different latitudes (54° vs. 79° N). Marine Ecology Progress Series 417, 159–170.CrossRefGoogle Scholar
Wear, R.G. (1974) Incubation in British decapod Crustacea, and the effects of temperature on the rate and success of embryonic development. Journal of the Marine Biological Association of the United Kingdom 54, 745–762.CrossRefGoogle Scholar