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Biochemical composition of the deep-sea red crab Chaceon quinquedens (Geryonidae): organic reserves of developing embryos and adults

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Abstract

Deep-sea red crabs Chaceon quinquedens (Smith) were collected in traps at depths of 860 and 1043 m in the northern Gulf of Mexico. Ovigerous crabs were maintained in the laboratory and the developing embryos were sampled every 2 wk until hatching. Proximate analysis (lipid, protein, carbohydrate, and ash) of embryos was performed to determine patterns and rates of organic reserve utilization during embryogenesis. Midgut gland, gonads, and clutch (as appropriate) of adult crabs (males, non-ovigerous females and ovigerous females) were analyzed for the same components as the embryos. Red crab embryos exhibited different patterns of yolk deposition and subsequent depletion of yolk components during embryogenesis. There was a range of lipid to protein (L:P) ratios among the different clutches examined, indicating plasticity in the relative proportions of lipid and protein yolk. The energy used for embryogenesis was estimated by converting the amounts of lipid, protein and carbohydrate in the embryos to their caloric equivalents; final values, taken from 9 mo-old embryos whose siblings were hatching as zoeae, were subtracted from the initial values of sibling embryos sampled at the time of collection (2 to 3 mo old). The amount of energy consumed during embryogenesis in the laboratory was relatively constant (0.12 to 0.13 cal egg-1). There was considerable variability among the concentrations of organic reserves in the midgut gland of adult crabs and in the ovaries of females. Variations in midgut gland L:P ratios and ovaries were related to the reproductive status of the females, but there were no trends related to depth of capture.

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References

  • Achituv Y, Barnes H (1976) Studies in the biochemistry of cirripede eggs. V. Changes in the general biochemical composition during development of Chthamalus stellatus (Poli). J exp mar Biol Ecol 22: 263–267

    Google Scholar 

  • Barnes H (1965) Studies in the biochemistry of cirripede eggs. I. Changes in the general biochemical composition during development of Balanus balanoides and B. balanus. J mar biol Ass UK 45: 321–339

    Google Scholar 

  • Berges JA, Fisher AE, Harrison PJ (1993) A comparison of Lowry, Bradford and Smith protein assays using different protein standards and protein isolated from the marine diatom Thalassiosira pseudonana. Mar Biol 115: 187–193

    Google Scholar 

  • Catille FL, Lawrence AL (1989) Relationship between maturation and biochemical composition of the gonads and digestive glands of the shrimps Penaeus aztecus Ives and Penaeus setiferus (L.). J Crustacean Biol 9: 202–211

    Google Scholar 

  • Churchill, EP Jr (1919) Life history of the blue crab. Bull Bur Fish, Wash 36: 1–38 (Document No 870)

    Google Scholar 

  • Clarke A (1982) Lipid synthesis and reproduction in the polar shrimp Chorismus antarcticus. Mar Ecol Prog Ser 9: 81–90

    Google Scholar 

  • Crisp DJ (1984) Energy flow measurements In: Holme NA, McIntyre AD (eds) Methods for the study of marine benthos. Black well Scientific Publications, Oxford, pp 284–372

    Google Scholar 

  • Diehl WJ, Biesiot PM (1994) Relationships between multilocus heterozygosity and morphometric indices in a population of the deep-sea red crab Chaceon quinquedens (Smith) J exp mar Biol Ecol 182: 237–250

    Google Scholar 

  • Dubois M, Gilles KA, Hamilton JK, Rebers PA, Smith F (1956) Calorimetric method for determination of sugars and related substances. Analy Chem 28: 350–356

    Google Scholar 

  • Erdman RB, Blake NJ, Lindberg WJ, Lockhart FD, Perry HM, Waller RS (1991) Comparative reproduction of the deep-sea crabs Chaceon fenneri and C. quinquedens (Brachyura: Geryonidae) from the northeast Gulf of Mexico. Invert Reprod Dev 19: 175–184

    Google Scholar 

  • Farlow JO Jr (1980) Natural history and ecology of a demersal fish megabenthic invertebrate community from the upper continental slope off southern New England. Ph.D. dissertation. Yale University, Connecticut

    Google Scholar 

  • Gage JD, Tyler PA (1991) Deep-sea biology: a natural history of organisms at the deep-sea floor. Cambridge University Press, Cambridge

    Google Scholar 

  • Gibson R, Barker PL, (1979) The decapod hepatopancreas. Oceangr mar biol A Rev 17: 285–346

    Google Scholar 

  • Haefner PA Jr (1977) Reproductive biology of the female deep-sea red crab, Geryon quinquedens from the Chesapeake Bight. Fish Bull US 75: 91–102

    Google Scholar 

  • Haefner PA Jr (1978) Seasonal aspects of the biology, distribution and relative abundance of the deep-sea red crab Geryon quinquedens Smith in the vicinity of the Norfolk Canyon, western North Atlantic. Proc natn Shellfish Ass 68: 49–62

    Google Scholar 

  • Haefner PA Jr, Musick JA (1974) Observations on distribution and abundance of red crabs in Norfolk Canyon and adjacent continental slope. Mar Fish Rev 36: 31–34

    Google Scholar 

  • Haefner PA Jr, Spaargaren DH (1993) Interactions of ovary and hepatopancreas during the reproductive cycle of Crangon crangon (L.). I. Weight and volume relationships. J Crustacean Biol 13: 523–531

    Google Scholar 

  • Hartree EF (1972) Determination of protein: a modification of the Lowry method that gives a linear photometric response Analyt Biochem 48: 422–427

    Google Scholar 

  • Heath JR, Barnes H (1970) Some changes in the biochemical composition with season and during the moulting cycle of the common shore crab, Carcinus maenas (L.). J exp mar Biol Ecol 5: 199–233

    Google Scholar 

  • Herring PJ (1974) Observations on the embryonic development of some deep-living decapod crustaceans, with particular reference to species of Acanthephyra. Mar Biol 25: 25–33

    Google Scholar 

  • Hines A (1988) Fecundity and reproductive output in two species of deep-sea crabs, Geryon fenneri and G. quinquedens (Decapoda, Brachyura). J Crustacean Biol 8: 557–562

    Google Scholar 

  • Hines A (1990) Commentary on life history and ecology of deep-sea crabs of the family Geryonidae. In: Lindberg WJ, EL Wenner (eds) Geryonid crabs and associated continental slope fauna: a research workshop report. Florida Sea Grant College, Gainesville, Fla pp 30–38 (Tech Pap No. 58)

    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. Vol. 4. Academic Press, New York, pp 85–123

    Google Scholar 

  • Icely JD, Nott JA (1992) Digestion and absorption: digestive system and associated organs. In: Harrison FW (ed) Microscopic anatomy of invertebrates. Vol. 10. Decapod Crustacea. Wiley-Liss, Inc., New York, pp 147–201

    Google Scholar 

  • Krol RM, Hawkins WE, Overstreet RM (1992) Reproductive components. In: Harrison FW (ed) Microscopic anatomy of invertebrates. Vol. 10. Decapod Crustacea. Wiley-Liss, Inc., New York, pp 295–343

    Google Scholar 

  • Lindberg WJ, Lockhart FD (1993) Depth-stratified population structure of geryonid crabs in the eastern Gulf of Mexico. J Crustacean Biol 13: 713–722

    Google Scholar 

  • Lockhart FD (1988) Depth distribution and ecology of two deep-sea crabs, Geryon spp. in the eastern Gulf of Mexico. M.S. thesis. University of Florida

  • Lockhart FD, Lindberg WJ, Blake NJ, Erdman RB, Perry HM, Waller RS (1990) Distributional differences and population similarities for two deep-sea crabs (family Geryonidae) in the northeastern Gulf of Mexico. Can J Fish aquat Sciences 47: 2112–2122

    Google Scholar 

  • Lux FE, Ganz AR, Rathjen WF (1982) Marking studies of the red crab Geryon quinquedens off southern New England. J Shellfish Res 2: 71–80

    Google Scholar 

  • Manning RB, Holthuis LB (1989) Two new genera and nine new species of geryonid crabs (Crustacea, Decapoda, Geryonidae). Proc biol Soc Wash 102: 50–77

    Google Scholar 

  • Nilsson HL, Lindstrom M (1983) Retinal damage and sensitivity loss of a light-sensitive crustacean compound eye (Cirolana borealis): electron microscopy and electrophysiology. J exp Biol 107: 277–292

    Google Scholar 

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

    Google Scholar 

  • Perry HM, Waller R, Stuck L, Stuck K, Erdman R, Blake N, Lockhart F, Lindberg W (1991) Occurrence of Chaceon larvae in plankton samples from slope waters of the northeastern Gulf of Mexico. Gulf Res Rep 8: 313–315

    Google Scholar 

  • Pillay KK, Nair NB (1973) Observations on the biochemical changes in gonads and other organs of Uca annulipes, Portunus pelagicus and Metapenaeus affinis (Decapoda: Crustacea) during the reproductive cycle. Mar Biol 18: 167–198

    Google Scholar 

  • Sasaki GC (1984) Biochemical changes associated with embryonic and larval development in the American lobster Homarus americanus Milne Edwards. Ph.D. dissertation. Woods Hole Oceanographic Institution/Massachusetts Institute of Technology Joint Program in Oceanography, Woods Hole, Mass (Ref WHOI-84-8)

    Google Scholar 

  • Sasaki GC, Capuzzo JM (1984) Degradation of Artemia lipids under storage. Comp Biochem Physiol 78B: 525–531

    Google Scholar 

  • Sastry AN (1983) Ecological aspects of reproduction. In: Vernberg FJ, Vernberg WB (eds) Biology of Crustacea. Vol. 8, Academic Press, New York, pp 179–270

    Google Scholar 

  • Smith PK, Krohn RI, Hermanson TI, Mallia AK, Gartner FH, Provenzano MD, Fujimoto EK, Goeke NM, Olson BJ, Klenck DC (1985) Measurement of protein using bicinchoninic acid. Analyt Biochem 150: 76–85

    Google Scholar 

  • Spaargaren DH, Haefner PA Jr (1994) Interactions of ovary and hepatopancreas during the reproductive cycle of Crangon crangon (L.). II. Biochemical relationships. J Crustacean Biol 14: 6–19

    Google Scholar 

  • SPSX Inc. (1986) SPSSX user's guide. McGraw Hill, New York

    Google Scholar 

  • Sulkin SD, van Heukelem WF (1980) Ecological and evolutionary significance of nutritional flexibility in planktotrophic larvae of the deep sea red crab Geryon quinquedens and the stone crab Menippe mercenaria. Mar Ecol Prog Ser 2: 91–95

    Google Scholar 

  • Waller R, Perry H, Trigg C, McBee J, Erdman R, Blake N (1995) Estimates of harvest potential and distribution of the deep sea red crab, Chaceon quinquedens, in the northcentral Gulf of Mexico. Gulf Res Rep 9: 75–84

    Google Scholar 

  • Wigley RL, Theroux RB, Murray HE (1975) Deep-sea red crab, Geryon quinquedens, survey off northeastern United States. Mar Fish Rev 37: 1–27

    Google Scholar 

  • Zar JH (1984) Biostatistical analysis. 2nd edn. Prentice-Hall, Inc., Englewood Cliffs, New Jersey

    Google Scholar 

Download references

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Communicated by N.H. Marcus, Tallahassee

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Biesiot, P.M., Perry, H.M. Biochemical composition of the deep-sea red crab Chaceon quinquedens (Geryonidae): organic reserves of developing embryos and adults. Marine Biology 124, 407–416 (1995). https://doi.org/10.1007/BF00363914

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