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Physiological and biochemical changes during lecithotrophic larval development and early juvenile growth in the northern stone crab, Lithodes maja (Decapoda: Anomura)

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Abstract

Larvae of the northern stone crab, Lithodes maja L., were reared in the laboratory from hatching to the second crab stage. complete larval development (at constant 9°C) lasted about 7 wk, invariably consisting of three pelagic zoeal stages and a semibenthic Megalopa; only two zoeal stages have been described in the literature. All larval stages are lecithotrophic. First feeding was consistently observed only after metamorphosis, in the first juvenile crab stage. In short intervals (every 1 to 5 d), developmental changes in biomass, B (expressed as: dry weight, W; carbon, C; nitrogen, N; hydrogen, H) and oxygen consumption (respiration, R) were measured in larvae and early juveniles; additionally, protein and carbohydrates were measured, but only in the zoeal stages and early Megalopa. Unusually high C contents (varying between 56 and 61% of W in eggs and freshly hatched Zoea I larvae from 12 different females) and high C:N weight ratios (8 to 11) indicate enhanced initial lipid stores, which are utilized as the major metabolic substrate during both embryonic and lecithotrophic larval development. Predominant degradation of lipids is shown indirectly; the C:N ratio decreased significantly, from 10 (at hatching) to 6 (at metamorphosis), while larval protein decreased only little, from ca. 55% of W (at hatching) to 48% (in the Megalopa). From hatching to metamorphosis, about 27% of the initially present W, 48% of C, 18% of N, and 52% of H were lost. This decrease in larval biomass can be described as an exponential function of development time. The major part of these losses were associated with metabolic energy requirements, while exuvial losses were comparably small. In each of the zoeal stages, only about 1 to 2% of late premoult (LPM) B was shed with the exuvia. The Megalopa, which produces a much thicker, calcified exoskeleton, lost 20% of LPM W, but only 5 to 8% of organic constituents (C, N, H). Much higher exuvial losses were measured in the Crab I stage (51% in W, 21% in C, 5% in N, and 7% in H). Maximum respiration was found in the actively swimming zoeal stages, a minimum in the predominantly benthic, mostly inactive Megalopa. The Crab I stage exhibits also a sluggish behaviour and low R, in spite of beginning food uptake and growth. Immediately after metamorphosis, the juvenile crab gained rapidly in W, in particular in its C fraction. A transitorily steep increase in the C:N ratio indicates a replenishment of partially depleted lipid stores, but also a rapid initial increase of inorganic C in the heavily calcified exoskeleton. Instantaneous rates of growth, assimilation, and net growth efficiency (K 2) were high during the initial (postmoult) phase in the first juvenile crab stage (C-specific growth rate: 6% d-1; K 2:70%), but decreased towards zero values during laterstages of the moulting cycle; metabolism remained practically constant during the Crab I stage. Entirely lecithotrophic larval development from hatching to metamorphosis in L. maja is considered an adaptation to seasonally short and limited planktonic food production in subarctic regions of the northern Atlantic.

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References

  • Anger K (1983) Temperature and the larval development of Hyas araneus L (Decapoda: Majidae); extrapolation of laboratory data to field conditions. J exp mar Biol Ecol 68: 203–215

    Google Scholar 

  • Anger K (1986) Changes of respiration and biomass of spider crab (Hyas araneus) larvae during starvation. Mar Biol 90: 261–269

    Google Scholar 

  • Anger K (1991) Developmental changes in the bioenergetics of decapod larvae. Mem Qd Mus 31: 289–308

    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

    Google Scholar 

  • Anger K, Harms J (1990) Elemental (CHN) and proximate biochemical composition of decapod crustacean larvae. Comp Biochem Physiol 97B: 69–80

    Google Scholar 

  • Anger K, Harms J, Christiansen ME, Süsens U, Wilmes B (1992) Growth patterns, chemical composition and oxygen consumption in early juvenile Hyas araneus (Decapoda: Majidae) reared in the laboratory. Helgoländer Meeresunters 46: 9–28

    Google Scholar 

  • Anger K, Harms J, Püschel C, Seeger B (1989) Physiological and biochemical changes during the larval development of a brachyuran crab reared under constant conditions in the laboratory. Helgoländer Meeresunters 43: 225–244

    Google Scholar 

  • Anger K, Schuh M (1992) Bioenergetics of abbreviated larval deveiopment in the bromelid crab, Metopaulias depressus (Decapoda: Grapsidae). Comp Biochem Physiol 103A: 507–518

    Google Scholar 

  • Campodonico GI (1971) Desarrollo larval de la centolla Lithodes antarctica jacquinot en condiciones de laboratorio. (Crustácea Decapoda, Anomura: Lithodidae). An Inst Patagonia (Ser Ciencs nat) 2: 181–190

    Google Scholar 

  • Campodonico GI, Guzmán L (1981) Larval development of Paralomis granulosa (Jacquinot) under laboratory conditions (Decapoda, Anomura, Lithodidae). Crustaceana 40: 272–285

    Google Scholar 

  • Comoglio L, Vinuesa J (1991) Larval culture of southern king crab Lithodes santolla and false king crab Paralomis granulosa under laboratory conditions. In: Lavens P, Sorgeloos P, Jaspers E, Ollevier F (eds) Larvi '91. Symposium on Fish and Crustacean Larviculture. Eur Aquacult Soc, Spec Publ 15, Gent, Belgium, pp 349–350

  • Dawson EW (1989) King crabs of the world (Crustacea: Lithodidae) and their fisheries: a comprehensive bibliography. Misc Publ 101. New Zealand Oceanogr Inst, Div Water Sci, DSIR, Wellington

    Google Scholar 

  • Dyer MF, Cranmer CJ, Fry P, Fry WG (1984) The distribution of benthic hydrographic indicator species in Svalbard water, 1978–1991. J mar biol Ass UK 64: 667–677

    Google Scholar 

  • Ekman S (1953) Zoogeography of the sea. Sidgwick & Jackson, London

    Google Scholar 

  • Gurney R (1942) Larvae of decapod Crustacea. Royal Society, London, pp 1–306

    Google Scholar 

  • Harms J, Anger K, Klaus S, Seeger B (1991) Nutritional effects on ingestion rate, digestive enzyme activity, growth, and biochemical composition of Hyas araneus L. (Decapoda: Majidae) larvae. J exp mar Biol Ecol 145: 233–265

    Google Scholar 

  • Haynes EB (1982) Description of larvae of the golden king crab, Lithodes aequispina, reared in the laboratory. Fish Bull US 80: 305–313

    Google Scholar 

  • Haynes EB (1984) Early zoeal stages of Placetron wosnessenskii and Rhinolithodes wosnessenskii (Decapoda, Anomura, Lithodidae) and review of lithodid larvae of the northern North Pacific Ocean. Fish Bull US 82: 315–324

    Google Scholar 

  • Holland DL, Gabbott PA (1971) A micro-analytical scheme for the determination of protein, carbohydrate, lipid and RNA levels in marine invertebrate larvae. J mar biol Ass UK 51: 659–668

    Google Scholar 

  • Klages M, Gutt J, Starmans A, Bruns T (1995) Stone crabs close to the Antarctic continent: Lithodes murrayi Henderson, 1888 (Crustacea; Decapoda; Anomura) off Peter I Islands (68°C51′S, 90°51′W). Polar Biol 15: 73–75

    Google Scholar 

  • Konishi K (1986) Larval development of the stone crab, Hapalogaster dentata (De Haan, 1844) (Crustacea: Anomura: Lithodidae) reared in the laboratory. J Fac Sci Hokkaido Univ (Ser 6) 24: 155–172

    Google Scholar 

  • Kurata H (1960) Studies on the larva and post-larva of Paralithodes camtschatica. II. Feeding habits of the zoea. Bull Holkkaido reg Fish Res Lab 21: 1–8

    Google Scholar 

  • Lombardo RJ, Ferrari L, Vinuesa JH (1991) Effects of lindane and acetone on the development of larvae of the southern king crab (Lithodes antarcticus Jaquinot). Bull envir Contam Toxic 46: 185–192

    Google Scholar 

  • Lowry DH, Rosenberg NJ, Farr AL, Randall RJ (1951) Protein measurement with the folin phenol reagent. J biol Chem 193: 265–275

    Google Scholar 

  • MacDonald JD, Pike RB, Williamson DI (1957) Larvae of the British species of Diogenes, Pagurus, Anapagurus and Lithodes (Crustacea, Decapoda). Proc zool Soc Lond 128: 209–257

    Google Scholar 

  • Macpherson E (1991) Biogeography and community structure of the decapod crustacean fauna off Namibia (Southeast Atlantic). J Crustacean Biol 11: 401–415

    Google Scholar 

  • Macpherson E (1994) Occurrence of two lithodid crabs (Crustacea: Decapoda: Lithodidae) in the cold seep zone of the South Barbados accretionary prism. Proc biol Soc Wash 107: 465–468

    Google Scholar 

  • Markle DF, Dadswell MJ, Halliday RG (1987) Demersal fish and decapod crustacean fauna of the upper continental slope off Nova Scotia from La Have to St. Pierre Banks. Can J Zool 66: 1952–1960

    Google Scholar 

  • Nakanishi T (1985) The effects of the environment on the survival rate, growth and respiration of eggs, larvae and post-larvae of king crab (Paralithodes camtschatica). In: Melteff BR (ed) Proc Int King Crab Symp, Lowell Wakefield Fisheries Symposium Series. Alaska Sea Grant Report 85-12, University of Alaska, Fairbanks, pp 167–185

    Google Scholar 

  • Nakanishi T (1987) Rearing condition of eggs, larvae and postlarvae of king crab. Bull Japan Sea reg Fish Res Lab 37: 57–161

    Google Scholar 

  • Nakanishi T, Naryu M (1981) Some aspects of large-scale rearing of larvae and post-larvae of the king crab (Paralithodes camtschatica). Bull Japan Sea reg Fish Res Lab 32: 39–47

    Google Scholar 

  • O'Riordan CE (1986) Marine fauna notes from the National Museum of Ireland. Ir Nat J 22: 34–37

    Google Scholar 

  • Paul AJ, Paul JM (1980) The effect of early starvation on later feeding success of king crab zoeae. J exp mar Biol Ecol 44: 247–251

    Google Scholar 

  • Paul AJ, Paul JM, Shoemaker PA, Feder HM (1979) Prey concentrations and feeding response in laboratory-reared stage-one zoeae of king crab, snow crab, and pink shrimp. Trans Am Fish Soc 108: 440–443

    Google Scholar 

  • Pike RB, Williamson DI (1958) Crustacea Decapoda: Larvae. XI. Paguridea, Coenobitidea, Dromiidea and Homolidea. Fich Ident Zooplancton 81: 1–9

    Google Scholar 

  • Pike RB, Williamson DI (1959) Observations on the distribution and breeding of British hermit crabs and the stone crab (Crustacea: Diogenidae, Paguridae and Lithodidae). Proc zool Soc Lond 132: 551–567

    Google Scholar 

  • Roff JC, Davidson KG, Pohle G, Dadswell MJ (1984) A guide to the marine flora and fauna of the Bay of Fundy and Scotian Shelf: larval Decapoda: Brachyura. Can tech Rep Fish aquat Sciences 1322: 1–57

    Google Scholar 

  • Sachs L (1984) Angewandte Statistik, 6th edn. Springer Verlag, Berlin, Heidelberg, New York

    Google Scholar 

  • Salonen K, Sarvala J, Hakala I, Viljanen ML (1976) The relation of energy and organic carbon in aquatic invertebrates. Limnol Oceanogr 21: 724–730

    Google Scholar 

  • Sars GO (1889) Bidrag til Kundskaben om Decapodernes Forvandlinger. Arch Math Naturv 13: 133–201

    Google Scholar 

  • Squires HJ (1990) Decapod Crustacea of the Atlantic coast of Canada. Can J Fish aquat Sciences 221: 1–532

    Google Scholar 

  • Storch V, Anger K (1983) Influence of starvation and feeding on the hepatopancreas of larval Hyas araneus (Decapoda, Majidae). Helgoländer Meeresunters 36: 67–75

    Google Scholar 

  • Thorson G (1946) Reproduction and larval development of Danish marine bottom invertebrates. Meddr Kommn Havunders (Ser Plankton) 4: 1–523

    Google Scholar 

  • Vinuesa JH, Comoglio LI, Lovrich GA (1989) Growth of immature southern king crab, Lithodes santolla, in the Beagle Channel. In: Lowell Wakefield Fisheries Symposium, Proceedings of the International Symposium on King and Tanner Crabs, Anchorage, Alaska. University of Alaska Press, Anchorage, pp 259–271

    Google Scholar 

  • Vinuesa JH, Ferrari L, Lombardo RJ (1985) Effect of temperature and salinity on larval development of southern king crab (Lithodes antarcticus). Mar Biol 85: 83–87

    Google Scholar 

  • White A (1857) A popular history of British Crustacea; comprising a familiar account of their classification and habits. Lovell Reeve, London

    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 

  • Williams AB (1988) Notes on decapod and euphausiid crustaceans, continental margin, western Atlantic, Georges Bank to western Florida, USA. Fish Bull US 86: 67–76

    Google Scholar 

  • Zöllner N, Kirsch K (1962) Über die quantitative Bestimmung von Lipoiden (Mikromethode) mittels der vielen natürlichen Lipoiden (allen bekannten Plasmalipoiden) gemeinsamen Sulfophosphovanillin-Reaktion. Z ges exp Med 135: 545–561

    Google Scholar 

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Communicated by O. Kinne, Oldendorf/Luhe

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Anger, K. Physiological and biochemical changes during lecithotrophic larval development and early juvenile growth in the northern stone crab, Lithodes maja (Decapoda: Anomura). Marine Biology 126, 283–296 (1996). https://doi.org/10.1007/BF00347453

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