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Tidal-amplitude rhythms of larval release: variable departure from presumed optimal timing among populations of the mottled shore crab

Published online by Cambridge University Press:  20 April 2010

M. Bueno  and
A.A.V. Flores
M. Bueno
Affiliation:
Universidade de São Paulo. Faculdade de Filosofia, Ciências e Letras de Ribeirão Preto, Avenida Bandeirantes 3900, CEP 14040-901, Ribeirão Preto, SP, Brazil
A.A.V. Flores*
Affiliation:
Universidade de São Paulo, Centro de Biologia Marinha, Rodovia Manoel Hipólito do Rego, Km 131,5, CEP 11600-000, São Sebastião, SP, Brazil
*
Correspondence should be addressed to: A.A.V. Flores, Universidade de São Paulo, Centro de Biologia Marinha, Rodovia Manoel Hipólito do Rego, Km 131,5, CEP 11600-000, São Sebastião, SP, Brazil email: [email protected]
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Abstract

It is widely assumed that optimal timing of larval release is of major importance to offspring survival, but the extent to which environmental factors entrain synchronous reproductive rhythms in natural populations is not well known. We sampled the broods of ovigerous females of the common shore crab Pachygrapsus transversus at both sheltered and exposed rocky shores interspersed along a 50-km coastline, during four different periods, to better assess inter-population differences of larval release timing and to test for the effect of wave action. Shore-specific patterns were consistent through time. Maximum release fell within 1 day around syzygies on all shores, which matched dates of maximum tidal amplitude. Within this very narrow range, populations at exposed shores anticipated hatching compared to those at sheltered areas, possibly due to mechanical stimulation by wave action. Average departures from syzygial release ranged consistently among shores from 2.4 to 3.3 days, but in this case we found no evidence for the effect of wave exposure. Therefore, processes varying at the scale of a few kilometres affect the precision of semilunar timing and may produce differences in the survival of recently hatched larvae. Understanding the underlying mechanisms causing departures from presumed optimal release timing is thus important for a more comprehensive evaluation of reproductive success of invertebrate populations.

Keywords

larval release synchronismtidal rhythmsBrachyurareproductive output
Type
Research Article
Information
Journal of the Marine Biological Association of the United Kingdom , Volume 90 , Issue 5 , August 2010 , pp. 859 - 865
Copyright
Copyright © Marine Biological Association of the United Kingdom 2010

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References

REFERENCES

Abele, L.G., Campanella, P.J. and Salmon, M. (1986) Natural history and social organization of the semiterrestrial grapsid crab Pachygrapsus transversus (Gibbes). Journal of Experimental Marine Biology and Ecology 104, 153–170.CrossRefGoogle Scholar
Baeza, J.A. and Fernández, M. (2002) Active brood care in Cancer setosus (Crustacea: Decapoda): the relationship between female behavior, embryo oxygen consumption and the cost of brooding. Functional Ecology 16, 241–251.CrossRefGoogle Scholar
Beck, M.W. (1995) Size-specific shelter limitation in stone crabs—a test of the demographic bottleneck hypothesis. Ecology 76, 968–980.CrossRefGoogle Scholar
Bell, E.C. and Denny, M.D. (1994) Quantifying ‘wave exposure’: a simple device for recording maximum velocity and results of its use at several field sites. Journal of Experimental Marine Biology and Ecology 181, 9–29.CrossRefGoogle Scholar
Boolootian, R.A., Giese, A.C., Farmanfarmaian, A. and Tucker, J. (1959) Reproductive cycles of five west coast crabs. Physiological Zoology 23, 213–220.CrossRefGoogle Scholar
Cannicci, S., Paula, J. and Vannini, M. (1999) Activity pattern and spatial strategy in Pachygrapsus marmoratus (Decapoda: Grapsidae) from Mediterranean and Atlantic shores. Marine Biology 133, 429–435.CrossRefGoogle Scholar
Cannicci, S., Gomei, M., Dahdouh-Guebas, F., Rorandelli, R. and Terlizzi, A. (2007) Influence of seasonal food abundance and quality on the feeding habits of an opportunistic feeder, the intertidal crab Pachygrapsus marmoratus. Marine Biology 151, 1331–1342.CrossRefGoogle Scholar
Chadwick, D.B. and Largier, J.L. (1999) The influence of tidal range on the exchange between San Diego Bay and the ocean. Journal of Geophysical Research 104, 29,885–29,899.CrossRefGoogle Scholar
Cuesta, J.A. and Schubart, C.D. (1998) Morphological and molecular differentiation between three allopatric populations of the littoral crabs Pachygrapsus transversus (Gibbes, 1850) (Brachyura, Grapsidae). Journal of Natural History 32, 1499–1508.CrossRefGoogle Scholar
Derivera, C.E. (2005) Long searches for male-defended breeding burrows allow female fiddler crabs, Uca crenulata, to release larvae on time. Animal Behaviour 70, 289–297.CrossRefGoogle Scholar
Flores, A.A.V., Mazzuco, A.C.A. and Bueno, M. (2007) A field study to describe diel, tidal and semilunar rhythms of larval release in an assemblage of tropical rocky shore crabs. Marine Biology 151, 1989–2002.CrossRefGoogle Scholar
Flores, A.A.V., Gomes, C.C. and Villano, W.F. (2009) Source populations in coastal crabs: population parameters affecting egg production. Aquatic Biology 7, 31–43.CrossRefGoogle Scholar
Flores, A.A.V. and Negreiros-Fransozo, M.L. (1999) On the population biology of the mottled shore crab Pachygrapsus transversus (Gibbes, 1850) (Brachyura, Grapsidae) in a subtropical area. Bulletin of Marine Science 65, 59–73.Google Scholar
Forward, R.B. Jr (1987) Larval release rhythms of decapod crustaceans: an overview. Bulletin of Marine Science 41, 165–176.Google Scholar
Forward, R.B. Jr and Bourla, M.H. (2008) Entrainment of the larval release rhythm of the crab Rhithropanopeus harrisii (Brachyura: Xanthidae) by cycles in hydrostatic pressure. Journal of Experimental Marine Biology and Ecology 357, 128–133.CrossRefGoogle Scholar
Ituarte, R.B., Spivak, E.D. and Luppi, T.A. (2004) Female reproductive cycle of the Southwestern Atlantic estuarine crab Chasmagnathus granulatus (Brachyura: Grapsoidea: Varunidae). Scientia Marina 68, 127–137.Google Scholar
Kennish, R. and Williams, G.A. (1997) Feeding preferences of the herbivorous crab Grapsus albolineatus: the differential influence of algal nutrient content and morphology. Marine Ecology Progress Series 147, 87–95.CrossRefGoogle Scholar
Kim, T.W. and Choe, J.C. (2003) The effect of food availability on the semilunar courtship rhythm in the fiddler crab Uca lactea (de Haan) (Brachyura: Ocypodidae). Behavioral Ecology and Sociobiology 54, 210–217.CrossRefGoogle Scholar
Kuris, A.M. (1991) A review of patterns and causes of crustacean brood mortality. In Wenner, A. and Kuris, A. (eds.) Crustacean egg production. Rotterdam: Balkema, pp. 117–141.Google Scholar
Lohrer, A.M., Fukui, Y., Wada, K. and Whitlatch, R.B. (2000) Structural complexity and vertical zonation of intertidal crabs, with focus on habitat requirements of the invasive Asian shore crab, Hemigrapsus sanguineus (de Haan). Journal of Experimental Marine Biology and Ecology 244, 203–217.CrossRefGoogle Scholar
Mizushima, N., Nakashima, Y. and Kuwamura, T. (2000) Semilunar spawning cycle of the humbug damselfish Dascyllus aruanus. Journal of Ethology 18, 105–108.CrossRefGoogle Scholar
Morgan, S.G. (1995) The timing of larval release. In McEdward, L. (ed.) Ecology of marine invertebrate larvae. Boca Raton, FL: CRC Press, pp. 157–191.Google Scholar
Morgan, S.G. and Christy, J.H. (1994) Plasticity, constraint, and optimality in reproductive timing. Ecology 75, 2185–2203.CrossRefGoogle Scholar
Naylor, J.K., Taylor, E.W. and Benett, D.B. (1999) Oxygen uptake of developing eggs of Cancer pagurus (Crustacea: Decapoda: Cancridae). Journal of the Marine Biological Association of the United Kingdom 79, 305–315.CrossRefGoogle Scholar
Naylor, E. and Williams, B.G. (1984) Environmental entrainment of tidally rhythmic behaviour in marine animals. Zoological Journal of the Linnean Society 80, 201–208.CrossRefGoogle Scholar
Palumbi, S.R. (1984) Measuring intertidal wave force. Journal of Experimental Marine Biology and Ecology 81, 171–179.CrossRefGoogle Scholar
Poupin, J., Davie, P.J.F. and Cexus, J.C. (2005) A revision of the genus Pachygrapsus Randall, 1840 (Crustacea: Decapoda: Brachyura: Grapsidae) with special reference to the Southwest Pacific species. Zootaxa 1015, 3–66.CrossRefGoogle Scholar
Roughgarden, J. and Iwasa, Y. (1986) Dynamics of a metapopulation with space-limited subpopulations. Theoretical Population Biology 29, 235–261.CrossRefGoogle Scholar
Schlieder, R.A. (1980) Effects of dessication and autopsy on egg hatching success in the stone crab, Menippe mercenaria. Fishery Bulletin 77, 695–700.Google Scholar
Underwood, A.J. (1997) Experiments in ecology: their logical design and interpretation using analysis of variance, 1st edition. Cambridge: Cambridge University Press.Google 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
Williams, J.A. (1979) A semi-lunar rhythm of locomotor activity and moult synchrony in the sand-beach amphipod Talitrus saltator. In Naylor, E. and Hartnoll, R.G. (eds) Cyclic phenomena in plant and animals. Oxford: Pergamon Press, pp. 407–414.CrossRefGoogle Scholar
Williams, A.B. (1984) Shrimps, lobsters and crabs of the eastern Atlantic coast of the United States, Maine to Florida, 1st edition. Washington, DC: Smithsonian Institution Press.Google Scholar
Yamahira, K. (1997) Hatching success affects the timing of spawning by the intertidally spawning puffer Takifugu niphobles. Marine Ecology Progress Series 155, 239–248.CrossRefGoogle Scholar
Zeng, C., Abello, P. and Naylor, E. (1999) Endogenous tidal and semilunar moulting rhythms in early juvenile shore crabs Carcinus maenas: implications for adaptation to a high intertidal habitat. Marine Ecology Progress Series 191, 257–266.CrossRefGoogle Scholar