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Fecundity, brood loss and egg development through embryogenesis of Armases cinereum (Decapoda: Grapsidae)

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Abstract

The present work is a comprehensive study of reproduction and embryonic development of Armases cinereum. Ovigerous A. cinereum (Bosc, 1802) females from Sebastian Inlet, Florida (9.88–19.4 mm CW) lay 2,000–12,000 eggs per brood, depending on their CW (mm): fecundity = 24.662 CW1.9432. A. cinereum displayed significant brood loss through development (ca. 500 eggs per brood) independently from their CW (no senescence). However, since smaller females lay fewer eggs than larger ones, the percentage of eggs lost during embryonic development is greater in smaller females. The number of eggs carried on a later stage of development (potential fertility = 5.5593 CW2.4417) is a more accurate estimate of the reproductive output and subsequent recruitment. Egg volume increased during development (64%, 0.025–0.041 mm3 or 0.36–0.43 mm of diameter, N = 270) and was strongly correlated with egg water content increase (19.21%, r = 0.89). Lipids, particularly fatty acids, seem to be the major energy source for embryonic development, decreasing 56.31 and 37.08% (respectively) during embryonic development; both are negatively correlated with egg volume (r = −0.90). The utilization of fatty acids through the different developmental stages of A. cinereum is presented. The most consumed fatty acids are the monounsatured (43.33 μg mg−1 dw), followed by the saturated (29.91 μg mg−1 dw) and polyunsaturated (24.03 μg mg−1). Palmitic (16:0) and linoleic (18:2n-6) acids are preferentially consumed (19.5 and 17.9 μg mg−1 dw, respectively). The high proportion of essential polyunsaturated fatty acids of C18 and C20 reflects the consumption of primary producers such as mangrove leaves. EPA/DHA ratio (2.85–3.84) and low DHA content indicated that this species appears in a medium-low level of the trophic chain. The low ratio of 18:1n-7/18:1n-9 and high percentage of 18:1n-9 (marker of carnivory) may be a sign of the consumption of juvenile invertebrates. The high percentage of odd-numbered FA indicated the occurrence of detritivores/scavenger behaviours. The fatty acid composition of the eggs reflects adult feeding ecology (omnivorous) and habitat.

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References

  • Abele LG (1992) A review of the grapsid crab genus Sesarma (Crustacea: Decapoda: Grapsidae) in America, with description of a new genus. Smithson Contrib Zool 527:1–60

    Article  Google Scholar 

  • Amsler MO, George RY (1984) Seasonal variation in the biochemical composition of the embryos of Callinectes sapidus Rathbun. J Crust Biol 4:546–553

    Article  CAS  Google Scholar 

  • Anger K (1995) The conquest of freshwater and land by marine crabs: adaptations in life-history patterns and larval bioenergetics. J Exp Mar Biol Ecol 193:119–145

    Article  Google Scholar 

  • Anger K (1998) Patterns of growth and chemical composition in decapod crustacean larvae. Invertebr Reprod Dev 33:159–176

    Article  CAS  Google Scholar 

  • Auel H, Harjes M, da Rocha R, Stübing D, Hagen W (2002) Lipid biomarkers indicate different ecological niches and trophic relationships of the Artic hyperiid amphipods Themisto abyssorum and T. libellula. Polar Biol 2: 374–383

    Google Scholar 

  • Bligh EG, Dyer WJ (1959) A rapid method of total lipids extraction and purification. Can J Biochem Physiol 37:911–917

    Article  CAS  Google Scholar 

  • Buck TL, Breed GA, Pennings SC, Chase ME, Zimmer M Carefoot TH (2003) Diet choice in an omnivorous salt-marsh crab: different food types, body size, and habitat complexity. J Exp Mar Biol Ecol 292:103–116

    Article  Google Scholar 

  • Cahu C, Fauvel C, Aquacop (1986) Effect of food fatty acids composition of P. vannanei broodstock on egg quality. International Council for the Exploration of the Sea. Mariculture Committee C.M. 28:1–8

  • Calado R, Narciso L (2003) Seasonal variation on embryo production and brood loss in the Monaco shrimp Lysmata seticaudata (Decapoda: Hippolytidae). J Mar Biol Ass U K 83:959–962

    Article  Google Scholar 

  • Calado R, Rosa R, Nunes ML, Narciso L (2005) Amino and fatty acid dynamics of Lysmata seticaudata (Decapoda: Hippolytidae) embryos during early and late reproductive season. Mar Biol 147:341–351

    Article  CAS  Google Scholar 

  • Clarke A, Brown JH, Holmes LJ (1990) The biochemical composition of eggs from Macrobrachium rosenbergii in relation to embryonic development. Comp Biochem Physiol B 96:505–511

    Article  Google Scholar 

  • Costlow JD, Bookhout CG (1960) The complete larval development of Sesarma cinereum (Bosc) reared in the laboratory. Bull Mar Biol 118:203–214

    Article  Google Scholar 

  • Dalsgaard J, St. John M, Kattner G, Müller-Navarra D, Hagen W (2003) Fatty acid trophic markers in the pelagic marine environment. Adv Mar Biol 46:225–340

    Article  Google Scholar 

  • DeMartini EE, Williams HA (2001) Fecundity and egg size of Scyllarides squammosus (Decapoda: Scyllaridae) at Maro Reef, Northwestern Hawaiian Islands. J Crust Biol 21:891–896

    Article  Google Scholar 

  • De Vries MC, Forward Jr. RB (1991) Mechanisms of crustacean egg hatching: evidence for enzyme release by crab embryos. Mar Biol 110:281–291

    Article  Google Scholar 

  • García-Guerrero M, Hendrickx ME (2004) Embryology of decapod crustaceans I. Embryonic development of the mangrove crabs Goniopsis pulchra and Aratus pisonii (Decapoda: Brachyura). J Crust Biol 24:666–672

    Article  Google Scholar 

  • Guinot D (1979) Morphologie et phylogenèse des brachyores. Mem Mus Natl Hist Nat A 112:1–353

    Google Scholar 

  • Hattori GY, Pinheiro MAA (2003) Fertilidade do caranguejo de mangue Ucides cordatus (Linnaeus) (Crustacea, Brachyura, Ocypodidae), em Iguape (Sao Paulo, Brasil). Rev Bras Zool 20:309–313

    Article  Google Scholar 

  • Herring PJ (1974) Size, density and lipid content of some decapod eggs. Deep Sea Res 21:91–94

    Google Scholar 

  • Hines AH (1982) Allometric constraints and variables of reproductive effort in brachyuran crabs. Mar Biol 69:309–320

    Article  Google Scholar 

  • Hines AH (1986) Larval patterns in the life histories of brachyuran crabs (Crustacea, Decapoda, Brachyura). Bull Mar Sci 39:444–466

    Google Scholar 

  • Holland DL (1978) Lipid reserves and energy metabolism in the larvae of benthic marine invertebrates. In: Malins DC, Sargent JR (eds) Biochemical and biophysical perspectives in marine biology. Academic Press, London

    Google Scholar 

  • Kattner G, Wehrtmann IS, Merck T (1994) Interannual variations of lipids and fatty acids during larval development of Crangon spp. in the German Bight, North Sea. Comp Biochem Physiol B 107:103–110

    Article  Google Scholar 

  • Kuris AM (1991) A review of patterns and causes of crustacean brood mortality. In: Wenner A, Kuris A (eds) Crustacean issues, vol.7. Crustacean egg production. Balkema, Rotterdam

    Google Scholar 

  • Kyomo J (2000) Intraspecific variation of reproductive strategies of the crab Sesarma intermedia: a consequence of habitat variations. Bull Mar Sci 66:157–171

    Google Scholar 

  • Lee SY (1998) Ecological role of grapsid crabs in mangrove ecosystems: a review. Mar Freshwat Res 49:335–343

    Article  Google Scholar 

  • Lee H, Hsu C (2003) Population biology of the swimming crab Portunus sanguinolentus in the waters off Northern Taiwan. J Crust Biol 23:691–699

    Article  Google Scholar 

  • Mantelatto FLM, Alarcon VF, Garcia RB (2002) Egg production strategies of the tropical hermit crab Paguristes tortugae from Brazil. J Crust Biol 22:390–397

    Article  Google Scholar 

  • Metcalfe LD, Schmitz AA (1961) The rapid preparation of fatty acids esters for gas chromatography analysis. Anal Chem 33:363–364

    Article  CAS  Google Scholar 

  • Mori M, Biagi F, De Ranieri S (1998) Fecundity and egg loss during incubation in Norway lobster (Nephrops norvegicus) in the North Tyrrhenian Sea. J Nat Hist 32:1641–1650

    Article  Google Scholar 

  • Morizur Y, Conan G, Guénolé A, Omnès MH (1981) Fécondité de Nephrops norvegicus dans le golfe de Gascogne. Mar Biol 63:319–324

    Article  Google Scholar 

  • Narciso L, Morais S (2001) Fatty acid profile of Palaemon serratum (Palaemonidae) eggs and larvae during embryonic and larval development using different live diets. J Crust Biol 21:566–574

    Article  Google Scholar 

  • Oh C, Hartnoll RG (1999) Brood loss during incubation in Philocheras trispinosus (Decapoda) in Port Erin Bay, Isle of Man. J Crust Biol 19:467–476

    Article  Google Scholar 

  • Okamori CL, Cobo VJ (2003) Fecundity of arrow crab Stenorhynchus seticornis in the Southern Brazilian coast. J Mar Biol Ass UK 83:979–980

    Article  Google Scholar 

  • Pandian TJ (1970) Ecophysiological studies on the developing egg and embryos of the European lobster Homarus gammarus. Mar Biol 5:154–167

    Article  Google Scholar 

  • Penha-Lopes G, Torres P, Macia A, Paula J (2007) Population structure and embryo loss of the seagrass shrimp Latreutes pymoeus (Decapoda: Hippolytidae) at Inhaca island, Mozambique. J Mar Biol Ass U K 87:879–884

    Article  Google Scholar 

  • Pennings S, Carefoot TH, Siska EL, Chase ME, Page TA (1998) Feeding preferences of a generalist salt-marsh crab: relative importance of multiple plant traits. Ecology 79:1968–1979

    Article  Google Scholar 

  • Petersen S, Anger K (1997) Chemical and physiological changes during embryonic development of the spider crab, Hyas araneus L. (Decapoda: Majidae). Comp Biochem Physiol B 117:299–306

    Article  Google Scholar 

  • Pinheiro MAA, Terceiro OSL (2000) Fecundity and reproductive output of the speckled swimming crab Arenaeus cribrarius (Lamarck, 1818) (Brachyura, Portunidae). Crustaceana 73:1121–1137

    Article  Google Scholar 

  • Pond D, Harris R, Head R, Harbour D (1996) Environmental and nutritional factors for determining seasonal variability in the fecundity and egg viability of Calanus helgolandicus in coastal waters off Plymouth, UK. Mar Ecol Prog Ser 143:45–63

    Article  Google Scholar 

  • Rainuzzo JR, Reitan KI, Olsen Y (1997) The significance of lipids at early stages of marine fish: a review. Aquaculture 155:103–116

    Article  CAS  Google Scholar 

  • Rosa R, Nunes ML (2003) Tissue biochemical composition in relation to the reproductive cycle of deep-sea decapod Aristeus antennatus in the south Portuguese coast. J Mar Biol Ass UK 83:963–970

    Article  CAS  Google Scholar 

  • Rosa R, Calado R, Narciso L, Nunes ML (2007) Embryogenesis of decapod crustaceans with different life history traits, feeding ecologies and habitats: a fatty acid approach. Mar Biol 151:935–947

    Article  Google Scholar 

  • Sargent JR, Henderson RJ, Tocher DR (1989) The lipids. In: Halver JE (ed) Fish nutrition. Academic Press, New York

    Google Scholar 

  • Schields JD (1993) The reproductive ecology and fecundity of Cancer crabs. In: Wenner A, Kuris A (eds) Crustacean issues vol7—crustacean egg production. A. Balkema, Rotterdam

    Google Scholar 

  • Schuh M, Diesel R (1995) Effects of salinity, temperature, and starvation on the larval development of Armases (=Sesama) miersii (Rathbun, 1897), a semiterrestrial crab with abbreviated development (Decapoda: Grapsidae). J Crust Biol 15:205–213

    Article  Google Scholar 

  • Scott C, Kwasniewski S, Falk-Petersen S, Sargent JR (2002) Species differences, origins and functions of fatty acids in the wax esters and phospholipids of Calanus hyperboreus, C. glacialis and C. finmarchicus from Artic waters. Mar Ecol Prog Ser 235:127–134

    Article  CAS  Google Scholar 

  • Seiple W (1979) Distribution, habitat preferences and breeding periods in the crustaceans Sesarma cinereum and S. reticulatum (Brachyura: Decapoda: Grapsidae). Mar Biol 52:77–86

    Article  Google Scholar 

  • Seiple W, Samon M (1987) Reproductive, growth and life-history contrasts between two species of grapsid crabs, Sesarma cinereum and S. reticulatum. Mar Biol 94:1–6

    Article  Google Scholar 

  • Skov MW, Hartnoll RG (2002) Paradoxical selective feeding on a low-nutrient diet: why do mangrove crabs eat leaves? Oecologia 131:1–7

    Article  Google Scholar 

  • Staton JL, Sulkin SD (1991) Nutritional requirements and starvation resistance in larvae of the brachyuran crabs Sesarma cinereum (Bosc) and S. reticulatum (Say). J Exp Mar Biol Ecol 152:271–284

    Article  Google Scholar 

  • Volkman JK, Barrett SM, Blackburn SI, Mansour MP, Sikes EL, Gelin F (1998) Microalgal biomarkers: a review of recent research developments. Organic Geochem 29:1163–1179

    Article  CAS  Google Scholar 

  • Wear RG (1974) Incubation in British decapod crustacean, and the effect of temperature on the rate of success of embryonic development. J Mar Biol Ass UK 54:745–762

    Article  Google Scholar 

  • Wehrtmann IS, Kattner G (1998) Changes in volume, biomass, and fatty acids of developing eggs in Nauticaris magellanica (Decapoda: Caridea) a latitudinal comparison. J Crust Biol 18:413–422

    Article  Google Scholar 

  • Williams AB (1984) Shrimps, lobsters, and crabs of the Atlantic coast of the eastern United States, Maine to Florida. Smithsonian Institution Press. Washington, DC

    Google Scholar 

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Acknowledgments

We would like to thank F. Faleiro, S. Brazão and P. Torres for their technical support and anonymous reviewers for constructive criticism. The authors would also like to thank Fundação para a Ciência e a Tecnologia (scholarship #SFRH/BD/17130/2004 and #SFRH/BD/25277/2005) and the Portuguese Government for providing financial support.

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Correspondence to Joana Figueiredo.

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Communicated by S.A. Poulet.

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Figueiredo, J., Penha-Lopes, G., Anto, J. et al. Fecundity, brood loss and egg development through embryogenesis of Armases cinereum (Decapoda: Grapsidae). Mar Biol 154, 287–294 (2008). https://doi.org/10.1007/s00227-008-0922-2

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