Hostname: page-component-586b7cd67f-2plfb Total loading time: 0 Render date: 2024-11-25T19:20:17.489Z Has data issue: false hasContentIssue false

Growth of cultured giant clams (Tridacna spp.) in low pH, high-nutrient seawater: species-specific effects of substrate and supplemental feeding under acidification

Published online by Cambridge University Press:  13 July 2011

Robert J. Toonen*
Affiliation:
Hawai‘i Institute of Marine Biology, School of Ocean & Earth Sciences & Technology, University of Hawai‘i at Mānoa, Kāne‘ohe, HI 96744USA
Tomoe Nakayama
Affiliation:
Waikīkī Aquarium, University of Hawai‘i at Mānoa, Honolulu, HI 96815USA
Tom Ogawa
Affiliation:
Oceanic Institute, 41-202 Kalaniana‘ole Highway, Waimānalo, HI 96795USA
Andrew Rossiter
Affiliation:
Waikīkī Aquarium, University of Hawai‘i at Mānoa, Honolulu, HI 96815USA
J. Charles Delbeek
Affiliation:
Waikīkī Aquarium, University of Hawai‘i at Mānoa, Honolulu, HI 96815USA
*
Correspondence should be addressed to: R.J. Toonen, Hawai‘i Institute of Marine Biology, School of Ocean & Earth Sciences & Technology, University of Hawai‘i at Mānoa, Kāne‘ohe, HI 96744USA email: [email protected]

Abstract

Four species of giant clams, Tridacna maxima, T. squamosa, T. derasa and T. crocea, were cultured in outdoor raceways for 364 days at the Waikīkī Aquarium and the Oceanic Institute on the island of O‘ahu, Hawai‘i, USA.  Growth of each species was compared among individuals grown with and without supplemental phytoplankton feeding, and directly on the substrate or mounted on concrete plugs in low pH, high nutrient seawater.  Among clams cultured with and without supplemental phytoplankton (Chaetoceros spp.), feeding resulted in significantly lower mortality in all species but T. deresa, whereas growth was significantly higher among fed clams for all species except T. squamosa. Tridacna derasa showed roughly a three-fold increase in growth when fed (88.5 g ± 4.4 SD) than when unfed (26.0 g ± 2.1 SD), whereas T. maxima growth was substantially lower, but nearly 10-fold greater in response to feeding (9.0 g ± 1.9 SD). The overall mortality rate of juvenile clams was significantly lower in the fed (44.4 ± 10.0%) than the unfed (71.8 ± 9.6%) trials, with the greatest effect observed in mortality of T. maxima (fed 15% versus unfed 80%) and T. squamosa (fed 65% versus unfed 95%). None of the T. squamosa remained on concrete plugs for the duration of the experiment. Among the remaining three species, there was no difference in either wet weight or shell length for T. maxima and for wet weight only in T. derasa on (186.5 g ± 16.1 SD) and off (147.0 g ± 6.0 SD) the concrete plugs.  In contrast, T. crocea had significantly greater shell growth off the plugs (14.3 mm ± 1.0 SD versus 8.5 mm ± 1.7 SD) but significantly greater gain in wet weight on the concrete plugs (26.3 g ± 1.5 SD versus 58.5 g ± 2.5 SD).  The seawater wells used for this study are well characterized with elevated levels of inorganic nutrients and higher pCO2 relative to tropical ocean waters, roughly approximating predictions for future oceanic conditions under IPCC IS92a emission scenarios. In comparison to previous studies in natural seawater, T. derasa had a significantly higher shell growth rate in the high-nutrient, low-pH well water.  In contrast, T. maxima and T. squamosa had significantly lower growth rates in low pH, whereas growth of T. crocea was not significantly different between low pH and ambient seawater.  These experiments demonstrate species-specific differences with each treatment, which cautions against making broad generalizations regarding the effects of substrate type, feeding effects, nutrient enrichment, and ocean acidification on tridacnid culture and survival.

Type
Research Article
Copyright
Copyright © Marine Biological Association of the United Kingdom 2011

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

Adulyanukosol, K. (1997) Growth of giant clam, Tridacna squamosa Lamarck under laboratory and natural conditions. Phuket Marine Biological Center Special Publication 17, 269274.Google Scholar
Ambariyanto, A. (2004) Improving survivorship of giant clam larvae. In Bilateral workshop on Coastal Resources Exploration and Conservation, 13–15 October 2004, Bali.Google Scholar
Ambariyanto, A. and Hoegh-Guldberg, O. (1997) Effect of nutrient enrichment in the field on the biomass, growth and calcification of the giant clam Tridacna maxima. Marine Biology 129, 635642.Google Scholar
Andersson, A.J., Kuffner, I.B., Mackenzie, F.T., Jokiel, P.L., Rodgers, K.S. and Tan, A. (2009) Net loss of CaCO3 from a subtropical calcifying community due to seawater acidification: mesocosm-scale experimental evidence. Biogeosciences 6, 18111823.CrossRefGoogle Scholar
Atkinson, M.J., Carlson, B. and Crow, G.L. (1995) Coral growth in high- nutrient, low–pH seawater: a case study of coral culture at the Waikīkī Aquarium, Honolulu, Hawaii. Coral Reefs 14, 215223.CrossRefGoogle Scholar
Belda, C.A., Lucas, J.S. and Yellowlees, D. (1993) Nutrient limitation in the giant clam–zooxanthellae symbiosis: effect of nutrient supplements on growth of the symbiotic partners. Marine Biology 117, 655664.Google Scholar
Braley, R.D. (ed.) (1992) The giant clam: a hatchery and nursery culture manual. Australian Center for International Agriculture Research Monograph No. 15. Canberra: Australian Centre for International Agricultural Research, 144 pp.Google Scholar
Calumpong, H.P. (ed.) (1992) The giant clam: an ocean culture manual. Australian Center for International Agriculture Research Monograph No. 16. Canberra: Australian Centre for International Agricultural Research.Google Scholar
Carlson, B.A. (1999) Organism responses to rapid change: what aquaria tell us about nature. American Zoologist 39, 4455.CrossRefGoogle Scholar
Delbeek, J.C. and Sprung, J. (1994) The reef aquarium. Volume one: a comprehensive guide to the identification and care of tropical marine invertebrates. Coconut Grove, FL: Ricordea Publishing, 544 pp.Google Scholar
Ellis, S. (1998) Spawning and early larval rearing of giant clams (Bivalvia: Tridacnidae). Waimānalo, HI: Center for Tropical and Subtropical Aquaculture Publication Number 130, Oceanic Institute, 42 pp.Google Scholar
Ellis, S. (1999) Lagoon farming of giant clams (Bivalvia: Tridacnidae). Waimānalo, HI: Center for Tropical and Subtropical Aquaculture, Publication Number 139, Oceanic Institute, 6 pp.Google Scholar
Estacion, J., Solis, E. and Fabro, L. (1986) A preliminary study of the effect of supplementary feeding on the growth of Tridacna maxima (Roding) (Bivalvia: Tridacnidae). Silliman Journal 33, 111116.Google Scholar
Fatherree, J.W. (2006) Giant clams in the sea and the aquarium. Tampa, FL: Liquid Medium, 227 pp.Google Scholar
Fisher, C.R., Fitt, W.K. and Trench, R.K. (1985) Photosynthesis and respiration in Tridacna gigas as a function of irradiance and size. Biological Bulletin. Marine Biological Laboratory, Woods Hole 169, 230245.CrossRefGoogle Scholar
Fitt, W.K. and Trench, R.K. (1981) Spawning, development, and acquisition of zooxanthellae by Tridacna squamosa (Mollucsa, Bivalvia). Biological Bulletin. Marine Biological Laboratory, Woods Hole 161, 213235.Google Scholar
Fitt, W.K., Rees, T.A.V., Braley, R.D., Lucas, J.S. and Yellowlees, D. (1993) Nitrogen flux in giant clams: size-dependency and relationship to zooxanthellae density and clam biomass in the uptake of dissolved inorganic nitrogen. Marine Biology 117, 381386.Google Scholar
Gomez, E.D. and Belda, C.A. (1988) Growth of giant clams in Bolinao, Philippines. In Copland, J.W. and Lucas, J.A. (eds) Giant clams in Asia and the Pacific. Burwood, Victoria: Craftsman Press Pty. Ltd, pp. 178182.Google Scholar
Grice, A.M. and Bell, J.D. (1997) Enhanced growth of the giant clam, Tridacna derasa (Roding, 1798), can be maintained by reducing the frequency of ammonium supplements. Journal of Shellfish Research 16, 523525.Google Scholar
Grice, A.M. and Bell, J.D. (1999) Application of ammonium to enhance the growth of giant clams (Tridacna maxima) in the land-based nursery: effects of size class, stocking density and nutrient concentration. Aquaculture 170, 1728.CrossRefGoogle Scholar
Guinotte, J.M. and Fabry, V.J. (2008) Ocean acidification and its potential effects on marine ecosystems. Annals of the New York Academy of Sciences 1134, 340342.CrossRefGoogle ScholarPubMed
Hart, A.M., Bell, J.D. and Foyle, T.P. (1998) Growth and survival of the giant clams, Tridacna derasa, T. maxima and T. crocea, at village farms in the Solomon Islands. Aquaculture 165, 203220.CrossRefGoogle Scholar
Hastie, L.C., Watson, T.C., Isamu, T. and Heslinga, G.A. (1992) Effect of nutrient enrichment on Tridacna derasa seed: dissolved inorganic nitrogen increases growth rate. Aquaculture 106, 4149.Google Scholar
Heslinga, G.A. and Fitt, W.K. (1987) The domestication of reef-dwelling giant-clams. Bioscience 37, 332339.CrossRefGoogle Scholar
Heslinga, G.A., Watson, T.C. and Isamu, T. (1990) Giant clam farming. Honolulu, HI: Pacific Fisheries Development Foundation (NMFS/NOAA), 179 pp.Google Scholar
Hoegh-Guldberg, O., Mumby, P.J., Hooten, A.J., Steneck, R.S., Greenfield, P., Gomez, E., Harvell, C.D., Sale, P.F., Edwards, A.J., Caldeira, K., Knowlton, N., Eakin, C.M., Iglesias-Prieto, R., Muthiga, N., Bradbury, R.H., Dubi, A. and Hatziolos, M.E. (2007) Coral reefs under rapid climate change and ocean acidification. Science 318, 17371742.CrossRefGoogle ScholarPubMed
IPCC (Intergovernmental Panel on Climate Change) (2007) Climate Change 2007: the physical science basis. Solomon, S., Qin, D., Manning, M., Marquis, M., Averyt, K., Tignor, M.M.B., Miller, H.L. Jr and Chen, Z. (eds). Contribution of Working Group I to the Fourth Assessment Report of the IPCC. http://www.ipcc.ch/SPM2feb07.pdfGoogle Scholar
Klumpp, D. W. and Griffiths, C.L. (1994) Contributions of phototrophic and heterotrophic nutrition to the metabolic and growth requirements of four species of giant clam (Tridacnidae). Marine Ecology Progress Series 115, 103115.CrossRefGoogle Scholar
Klumpp, D.W. and Lucas, J.S. (1994) Nutritional ecology of the giant clams Tridacna tevoroa and T. derasa from Tonga: influence of light on filter-feeding and photosynthesis. Marine Ecology Progress Series 107, 147156.CrossRefGoogle Scholar
Klumpp, D.W., Bayne, B.L. and Hawkins, A.J.S. (1992) Nutrition of the giant clam Tridacna gigas (L.) I. Contribution of filter feeding and photosynthates to respiration and growth. Journal of Experimental Marine Biology and Ecology 155, 105122.CrossRefGoogle Scholar
Knop, D. (1996) Giant clams—a comprehensive guide to the identification and care of tridacnid clams (Hert, E. and Holzberg, S., Trans.). Ettlingen: Dahne Verlag, 255 pp.Google Scholar
Kuffner, I.B., Andersson, A.J., Jokiel, P.L., Rodgers, K.S. and Mackenzie, F. (2008) Decreased abundance of crustose coralline algae due to ocean acidification. Nature Geoscience 1, 114117.CrossRefGoogle Scholar
Leggett, J., Pepper, W.J., Swart, R.J., Edmonds, J., Meira Filho, L.G., Mintzer, I., Wang, M.X. and Watson, J. (1992) Emissions Scenarios for the IPCC: an Update. In Houghton, J.T., Callander, B.A. and Varney, S.K. (eds) Climate Change 1992: the Supplementary Report to the IPCC Scientific Assessment. Cambridge, UK: Cambridge University Press, pp. 6895Google Scholar
Muscatine, L. (1967) Glycerol excretion by symbiotic algae from corals and Tridacna and its control by the host. Science 156, 516519.CrossRefGoogle ScholarPubMed
Orr, J.C., Fabry, V.J., Aumont, O., Bopp, L., Doney, S.C., Feely, R.A., Gnanadesikan, A., Gruber, N., Ishida, A., Joos, F., Key, R.M, Lindsay, K., Maier-Reimer, E., Matear, R., Monfray, P., Mouchet, A., Najjar, R.G., Plattner, G.-K., Rodgers, K.B., Sabine, C.L., Sarmiento, J.L., Schlitzer, R., Slater, R.D., Totterdell, I.J., Weirig, M.-F., Yamanaka, Y. and Yool, A. (2005) Anthropogenic ocean acidification over the twenty-first century and its impact on calcifying organisms. Nature 437, 681686.CrossRefGoogle ScholarPubMed
Othman, A.S., Goh, G.H.S. and Todd, P.A. (2010) The distribution and status of giant clams (Family Tridacnidae)—a short review. Raffles Bulletin of Zoology 58, 103111.Google Scholar
Ponwith, B.J. (1990) Giant clam (Tridacna derasa) growth and survival in American Samoa. Pago Pago, American Samoa: Department of Marine and Wildlife Resources.Google Scholar
Richter, C., Roa-Quiaoit, H., Jantzen, C., Mohammad, Al-Zibdah and Kochzius, M. (2008) Collapse of a new living species of giant clam in the Red Sea. Current Biology 18, 16.CrossRefGoogle ScholarPubMed
Shimek, R.L. (2009) Phytoplankton, a necessity for clams. http://www.dtplankton.com/articles/necessity.htmlGoogle Scholar
Solis, E.P., Onata, J.A. and Naguit, M.R.A. (1988) Growth of laboratory-reared giant clams under natural and laboratory conditions. In Copland, J.W. and Lucas, J.A. (eds) Giant clams in Asia and the Pacific. Burwood, Victoria: Craftsman Press Pty. Ltd, pp. 201206.Google Scholar
Tisdell, C.A., Tacconi, L., Barker, J.R. and Lucas, J.S. (1993) Economics of ocean culture of giant clams, Tridacna gigas: internal rate of return analysis. Aquaculture 110, 1326.Google Scholar
Toonen, R.J. and Wee, C.B. (2005) An experimental comparison of sediment-based biological filtration designs for recirculating aquarium systems. Aquaculture 250, 244255.CrossRefGoogle Scholar
Trench, R.K., Wethey, D.S. and Porter, J.W. (1981) Observations on the symbiosis with zooxanthellae among the Tridacnidae (Mollusca: Bivalvia). Biological Bulletin. Marine Biological Laboratory, Woods Hole 161, 180198.CrossRefGoogle Scholar
Yonge, C.M. (1975) Giant clams. Scientific American 232, 96105.CrossRefGoogle ScholarPubMed
Zar, J.H. (1984) Biostatical analysis. 2nd edition. Englewood Cliffs, NJ: Prentice-Hall, 130 pp.Google Scholar