Skip to main content
Log in

Patterns of growth and triacylglycerol content in snow crab Chionoecetes opilio (Brachyura: Majidae) zoeal stages reared in the laboratory

  • Published:
Marine Biology Aims and scope Submit manuscript

Abstract

Snow carb Chionoecetes opilio zoea I and zoea II larvae, hatched from females in a controlled mating experiment, were reared in the laboratory at 10.1 °C and 28.0‰ salinity, to resolve the patterns of growth (dry weight [DW]) and change in energy reserves (triacylglycerols [TAG]) within a given moult cycle. The patterns of growth and change in TAG reserves were similar in each zoeal stage. Following hatching or a moult, the zoeae entered a phase of rapid size increase, i.e. high daily growth rates (5.5 to 12.8% DWd-1), for 1/3 to 2/5 of the duration of the moult cycle. During the same period, the zoeae accumulated TAG reserves until a maximum (TAG DW-1) was reached at the end of the phase of rapid growth. The period of high growth rates and of TAG accumulation is interpreted as the required time for the zoeae to reach a point in development [i.e. point of reserves saturation (PRS); Anger and Dawirs (1981)] where sufficient growth and energy reserves allow moulting to the next stage. Following the phase of rapid growth and TAG accumulation, the zoeae entered a phase of low daily growth rates (0 to 1% DWd-1) during which the TAG reserves decreased to a minimum at the end of the phase. Prior to, and during the moult to zoea II, a phase of negative growth was observed in the zoea I larvae. We conclude that measurement of zoeal size and TAG content, along with morphometric criteria (e.g. epidermal retraction), can be used to assess growth and nutritional condition of C. opilio zoeal stages from the sea.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

Similar content being viewed by others

References

  • Anger K (1987) The Do threshold: a critical point in the larval development of decapod crustaceans. J exp mar Biol Ecol 108:15–30

    Google Scholar 

  • Anger K (1989) Growth and exuvial loss during larval and early juvenile development of the hermit crab Pagurus bernhardus reared in the laboratory. Mar Biol 103:503–511

    Google Scholar 

  • Anger K, Dawirs RR (1981) Influence of starvation on the larval development of Hyas araneus (Decapoda, Majidae). Helgoländer Meeresunters 34:287–311

    Google Scholar 

  • Anger K, Dawirs RR (1982) Elemental composition (C, N, H) and energy in growing and starving larvae of Hyas areaneus (Decapoda, Majidae). Fish Bull US 80:419–433

    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 

  • Chandumpai A, Dall W, Smith DM (1991) Lipid-class composition of organs and tissues of the tiger prawn Panaeus esculentus during the moulting cycle and during starvation. Mar Biol 108:235–245

    Google Scholar 

  • Davidson KG, Chin EA (1991) A comparison of the taxonomic characteristics and duration of the laboratory reared larvae of snow crabs, Chionoecetes opilio (O. Fabricius) and toad crabs, (Hyas sp.) from Atlantic Canada. Can Tech Rep Fish aquat Sciences 1792:1–21

    Google Scholar 

  • Dawirs RR, Püschel C, Schorn F (1986) Temperature and growth in Carcinus maenas L. (Decapoda: Portunidae) larvae reared in the laboratory from hatching through metamorphosis. J exp mar Biol Ecol 100:47–74

    Google Scholar 

  • Gore RH (1985) Molting and growth in decapod larvae. In: Wenner AM (ed) Crustacean Issues 2. Larval growth. A. A. Balkema, Rotterdam, pp 1–65

    Google Scholar 

  • Harms J (1990) Accumulation and loss of biomass in Liocarcinus holstatus larvae during growth and exuviation. Mar Biol 104:183–190

    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 E (1973) Descriptions of prezoae and stage I zoeae of Chionoecetes bairdi and C. opilio (Oxyrhyncha, Oregoniinae). Fish Bull US 71:769–775

    Google Scholar 

  • Incze LS, Wencker DL, Armstrong DA (1984) Growth and average growth rates of Tanner crab zoeae collected from the plankton. Mar Biol 84:93–100

    Google Scholar 

  • Kon T (1967) Fisheries biology of the tanner crab, Chionoecetes opilio. I. On the prezoeal larva. Bull Jap Soc scient Fish, 33:726–730. (English translation by Fish Res Bd Can Transl Ser No 1208)

    Google Scholar 

  • Lim BK, Hirayama K (1991) Growth and elemental composition (C, N, P) during larval developmental stages of mass-cultured swimming crab Portunus trituberculatus. Mar Ecol Prog Ser 78:131–137

    Google Scholar 

  • Minagawa M, Chiu JR, Murano M (1993) Developmental changes in body weight and elemental composition of laboratory-reared larvae of the red frog crab, Ranina ranina (Decapoda: Brachyura). Mar Biol 116:399–406

    Google Scholar 

  • Montú M, Anger K, de Bakker C, Anger A, Loureiro Fernandes L (1988) Larval development of the brazilian mud crab Panopeus austrobesus Williams, 1983 (Decapoda: Xanthidae) reared in the laboratory. J Crustacean Biol (Lawrence, Kansas) 8:594–613

    Google Scholar 

  • Motoh H (1973) Laboratory-reared zoeae and megalopae of zuwai crab from the Sea of Japan. Bull Jap Soc scient Fish 39:1233–1230

    Google Scholar 

  • Motoh H (1982) The larval stages of the genus Chionoecetes: C. opilio and C. japonicus reared in the laboratory. In: Meltett B (ed) Proceedings of the International Symposium on the Genus Chionoecetes. Univ. Alaska, Alaska Sea Grant Report No. 82-10, Fairbanks, Alaska, pp 119–136

    Google Scholar 

  • Ouellet P, Taggart CT Frank KT (1992) Lipid condition and survival in shrimp (Pandalus borealis) larvae. Can J Fish aquat Sciences 49:368–378

    Google Scholar 

  • Parrish CC, Ackman RG (1985) Calibration of the Iatroscan-Chromarod system for marine liqid class analyses. Lipids 20:521–530

    Google Scholar 

  • Paul AJ, Paul JM, Coyle KO (1990) Growth of stage I king crab larvae of Paralithodes camtschatica (Tilesius) (Decapoda: Lithodidae) in natural communities. J Crustacean Biol (Lawrence, Kansas) 10:175–183

    Google Scholar 

  • Pohle GW (1990) Larval development of Canadian Atlantic oregoniid crabs (Brachyura: Majidae), with emphasis on Hyas coarctatus alutaceus Brandt, 1851, and a comparison with Atlantic and Pacific conspecifics. Can J Zool 69:2717–2737

    Google Scholar 

  • Sainte-Marie B (1993) Reproductive cycle and fecundity of primiparous and multiparous female snow crab, Chionoecetes opilio, in the northwest Gulf of Saint Lawrence. Can J Fish aquat Sciences 50:2147–2156

    Google Scholar 

  • Sorgeloos P, Léger P (1992) Improved larviculture outputs of marine fish, shrimp and prawn. J Wld Aquacult Soc 23:251–264

    Google Scholar 

  • Vance DE, Vance JE (eds) (1985) Biochemistry of lipids and membranes. The Benjamin/Cummings Publishing Company, Inc. Menlo Park, California

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Communicated by R. J. Thompson, St. John's

Rights and permissions

Reprints and permissions

About this article

Cite this article

Lovrich, G.A., Ouellet, P. Patterns of growth and triacylglycerol content in snow crab Chionoecetes opilio (Brachyura: Majidae) zoeal stages reared in the laboratory. Marine Biology 120, 585–591 (1994). https://doi.org/10.1007/BF00350079

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00350079

Keywords

Navigation