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Evaluation of three phytoplankton species as food for the pearl oyster Pinctada fucata

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Abstract

In the pearl cultivation farms of the Ehime Prefecture, Japan, mass mortalities of the pearl oyster Pinctada fucata have occurred since 1994. The occurrences of mass mortality roughly coincided with a shift of the dominant phytoplankton from Skeletonema and Chaetoceros to Chaetoceros and Nitzschia all of which belong to Bacillariophyceae. Hence, we evaluated Nitzschia, together with Chaetoceros and Isocrysis, as food for the oyster. Wet weights, lengths, widths, glycogen contents, and growth rates in terms of wet weight of the oysters in all the feeding treatments were significantly higher than those in the non-feeding treatment. The highest glycogen content (2.34%) and growth rate (2.21 g month−1) were found in the Chaetoceros treatment. Growth rate in the Isocrysis treatment (1.63 g month−1) was also high, although glycogen content in this treatment (0.41%) was low. In the Nitzschia treatment, growth rate of the oyster (0.94 g month−1) was the lowest and glycogen content (0.83%) was also low relative to that in the Chaetoceros treatment. Chlorophyll a concentration in fecal pellets was lowest in the Nitzschia treatment (<2.7 μg mg−1), suggesting more complete digestion of Nitzschia by the oyster. Thus, Nitzschia was edible and digestible but not assimilated by P. fucata. We propose the following scenario for the relationship between Nitzschia dominance and mass mortality. When Nitzschia dominates in a culture area, the physiological condition of P. fucata deteriorates due to low assimilation of Nitzschia by the oyster, followed by susceptibility of the oyster to infection by agents lethal to the oyster.

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References

  • Ashikaga C (1949a) Biochemical studies on the pearl-oyster (Pinctada martensi). Part II. On the changes of glycogen content during the process of preservation. Biosci Biotech Biochem 23:63–65 (in Japanese)

    CAS  Google Scholar 

  • Ashikaga C (1949b) Biochemical studies on the pearl-oyster (Pinctada martensi). Part III. On the glycogen content in relation to portions and to sexes. Biosci Biotech Biochem 23:65–68 (in Japanese)

    CAS  Google Scholar 

  • Ehime Prefectural Fisheries Experimental Station (1974–2003) Bulletin of the Ehime Prefectural Fisheries Experimental Station

  • Enright CT, Newkirk JS, Craigie JS, Castell JD (1986) Growth of juvenile Ostrea edulis L. fed Chaetoceros gracilis schutt of varied chemical composition. J Exp Mar Biol Ecol 96:15–26

    Article  CAS  Google Scholar 

  • Fukushima K (1970) Mass mortalities of Japanese pearl oyster Pinctada fucata martensii in Matoya Bay and Gokasho Bay. Shinjugijutsu Kenkyukai Kaiho 9:1–21 (in Japanese)

    Google Scholar 

  • Fukushima K (1972) The health of Pinctada fucata martensii and food organisms environment. Shinjugijutsu Kenkyukai Kaiho 10:15–31 (in Japanese)

    Google Scholar 

  • Hashimoto T, Nakano S (2003) Nutrient limitation on abundance and growth of phytoplankton in a Japanese pearl cultivation farm. Mar Ecol Prog Ser 258:43–50

    Article  CAS  Google Scholar 

  • Kawabata K (1988) Ecology of Oocystis spp. in lake Biwa: abundance, colony composition, viability, and food relations with Eodiaptomus japonicus and Daphnia longispina. Mem Fac Sci Kyoto Univ (Ser Biol) 13:41–47

    Google Scholar 

  • Koizumi Y (1998) Mid-term oscillation of abundance and composition of phytoplankton in a coastal sea. Kaiyo Mon 30:419–423

    Google Scholar 

  • Kurokawa H, Suzuki T, Okauchi M, Miwa S, Nagai S, Nakamura K, Honjo T, Nakajima K, Ashida K, Hunakoshi S (1999) Experimental infections of a disease causing mass mortalities of Japanese pearl oyster Pinctada fucata martensii by tissue transplation and cohabitation. Nippon Suisan Gakkai Shi 65:241–251 (in Japanese with English abstract)

    Google Scholar 

  • Kuwatani M (1965) A study on feeding mechanism of Japanese pearl oyster, Pinctada martensii (dunker), with special reference to passage of charcoal particles in the digestive system. Bull Jpn Soc Sci Fish 31:789–798 (in Japanese with English abstract)

    Google Scholar 

  • Kuwatani Y, Nishii T (1968) On the rice powder as a diet of the pearl oyster. Bull Jpn Soc Sci Fish 34:191–203 (in Japanese with English abstract)

    Google Scholar 

  • Matsuyama Y, Nagai K, Mizuguchi T, Fujiwara M, Ishimura M, Yamaguchi M, Uchida T, Honjo T (1995) Ecological features and mass mortality of pearl oysters during red tides of Heterocapsa sp. in Ago Bay in 1992. Bull Jpn Soc Sci Fish 61:35–41

    Google Scholar 

  • Miyazaki T, Goto K, Kobayashi T, Kageyama T, Miyata M (1999) Mass mortalities associated with a virus disease in Japanese pearl oysters Pinctada fucata martensii. Dis Aquat Org 37:1–12

    Article  Google Scholar 

  • Miyazaki T, Taniguchi T, Hirayama J, Nozawa N (2002) Receptors for recombinant feline interferon-ω in hemocytes of the Japanese pearl oyster Pinctada fucata martensii. Dis Aquat Org 51:135–138

    Article  PubMed  CAS  Google Scholar 

  • Moran R, Porath D (1980) Chlorophyll determination in intact tissues using N,N-dimethylformamide. Plant Physiol 65:478–479

    Article  PubMed  CAS  Google Scholar 

  • Numaguchi K (1994a) Growth and physiological condition of the Japanese pearl oyster, Pinctada fucata martensii (Dunker, 1850) in Ohmura Bay, Japan. J Shellfish Res 13:93–99

    Google Scholar 

  • Numaguchi K (1994b) Effect of water temperature on the filtration rate of Japanese pearl oyster, Pinctada fucata martensii. Suisanzoshoku 42:1–6 (in Japanese with English abstract)

    Google Scholar 

  • Numaguchi K (1995a) Effects of water temperature on catabolic losses of meat and condition index of unfed pearl oyster Pinctada fucata martensii. Fish Sci 61:735–738

    CAS  Google Scholar 

  • Numaguchi K (1995b) Influences of unfed condition on the mortality of pearl oyster Pinctada fucata martensii. Fish Sci 61:739–742

    CAS  Google Scholar 

  • Numaguchi K (1999) Effective feeding concentration of the microalga Pavlova lutheri for growth of early spat of the pearl oyster Pinctada fucata martensii. J World Aquac Soc 30:290–292

    Article  Google Scholar 

  • Numaguchi K (2000) Evaluation of five microalgal species for the growth of early spat of the Japanese pearl oyster Pinctada fucata martensii. J Shellfish Res 19:153–157

    Google Scholar 

  • Ota S (1959) Studies on feeding habits of Pinctada martensii. V. Number and size of swimming bivalve larvae fed by pearl oyster in summer. Bull Natl Pearl Res Lab 5:443–449 (in Japanese)

    Google Scholar 

  • Porter KG (1975) Viable gut passage of gelatinous green algae ingested by Daphnia. Verh Int Ver Theor Angew Limnol 19:2840–2850

    Google Scholar 

  • Porter KG (1976) Enhancement of algal growth and productivity by grazing zooplankton. Science 192:1332–1334

    Article  PubMed  Google Scholar 

  • Porter KG (1977) The plant-animal interface in freshwater ecosystems. Am Sci 65:159–170

    Google Scholar 

  • Roe JH (1955) The determination of sugar in blood and spinal fluid with anthrone reagent. J Biol Chem 212:335–343

    PubMed  CAS  Google Scholar 

  • Suzuki S, Kamakura M, Kusuda R (1998a) Isolation of birnavirus from Japanese pearl oyster Pinctada fucata. Fish Sci 65:358–361

    Google Scholar 

  • Suzuki S, Utsunomiya I, Kusuda R (1998b) Experimental infection of marine birnavirus strain JPO-96 to Japanese pearl oyster Pinctada fucata. Bull Fish Mar Sci Kochi Univ 18:39–41

    Google Scholar 

  • Tomaru Y, Ebisuzaki S, Kawabata Z, Nakano S (2002a) Respiration rates of the Japanese pearl oyster, Pinctada fucata martensii, feeding on Pavlova lutheri and Chaetoceros gracilis. Aquac Res 33:33–36

    Article  Google Scholar 

  • Tomaru Y, Kawabata Z, Nakano S (2001) Mass mortality of the Japanese pearl oyster Pinctada fucata martensii in relation to water temperature, chlorophyll a and phytoplankton composition. Dis Aquat Organ 44:61–68

    Article  PubMed  CAS  Google Scholar 

  • Tomaru Y, Kumatabara Y, Kawabata Z, Nakano S (2002b) Effect of water temperature and chlorophyll abundance on shell growth of the Japanese pearl oyster, Pinctada fucata martensii, in suspended culture at different depths and sites. Aquac Res 33:109–116

    Article  Google Scholar 

  • Tomaru Y, Udaka N, Kawabata Z, Nakano S (2002c) Seasonal change of seston size distribution and phytoplankton composition in bivalve pearl oyster Pinctada fucata martensii culture farm. Hydrobiologia 481:181–185

    Article  Google Scholar 

  • Uematsu M, Minagawa M, Arita H, Tsunogai S (1978) Determination of dry weight of total suspended matter in seawater. Bull Fac Fish Hokkaido Univ 29(2):164–172 (in Japanese with English abstract)

    Google Scholar 

  • Whyte JNC (1987) Biochemical composition and energy content of six species of phytoplankton used in mariculture of bivalves. Aquaculture 60:231–241

    Article  CAS  Google Scholar 

Download references

Acknowledgements

I wish to express sincere thanks to Mr S. Hyodo and the staff of Uchiumi Institute of Oceanic and Fishery Science for their help with the field monitoring and feeding experiment and for supporting the glycogen analysis. We thank Dr M. J. Morris for correction of our English and constructive comments on the manuscript. The present study was partly supported by the Grant-in-Aid for Scientific Research No. 12308027, JSPS, and the Research Fund of coastal environment in Uchiumi Bay, Ainan Town, Ehime Prefecture.

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Correspondence to Shin-ichi Nakano.

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Hashimoto, T., Hyodoh, K., Hirose, T. et al. Evaluation of three phytoplankton species as food for the pearl oyster Pinctada fucata . Aquacult Int 16, 309–318 (2008). https://doi.org/10.1007/s10499-007-9144-8

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  • DOI: https://doi.org/10.1007/s10499-007-9144-8

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