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Monthly variation of condition index,energy reserves and antibacterial activity in Pacific oysters,Crassostrea gigas,in Stansbury (South Australia)
Authors:Yan Li  Jian G Qin  Xiaoxu Li  Kirsten Benkendorff
Institution:1. State Key Laboratory of Cellular Stress Biology, School of Life Sciences, Xiamen University, Xiamen 361005, China;2. State Key Laboratory of Marine Environmental Science, Xiamen University, Xiamen 361005, China;3. Department of Chemistry, Oregon State University, Corvallis, 97331 OR, USA;4. Department of Chemical Biology, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, China;1. Department of Biology, University of North Carolina at Charlotte, 9201 University City Blvd., Charlotte, NC 28223, USA;2. Department of Oral Biology, University of Pittsburgh, 589 Salk Hall, 3501 Terrace Street, Pittsburgh, PA 15261, USA;1. Department of Biology, University of North Carolina at Charlotte, 9201 University City Blvd., Charlotte, NC, 28223, USA;2. Department of Oral Biology, University of Pittsburgh, 589 Salk Hall, 3501 Terrace Street, Pittsburgh, PA 15261, USA;3. Department of Biology, The College of New Jersey, 2000 Pennington Rd., Ewing, NJ 08628, USA;4. Great Basin College, 1500 College Parkway, Elko, NV 8980, USA;1. University of Bremen, Bremen Marine Ecology (BreMarE), P.O. Box 330440, 28359 Bremen, Germany;2. Alfred Wegener Institute for Polar and Marine Research (AWI), Am Handelshafen 12, 27550 Bremerhaven, Germany;3. Bremerhaven University of Applied Sciences, Applied Marine Biology, An der Karlstadt 8, 27568 Bremerhaven, Germany
Abstract:This paper investigates the temporal responses of 2-year old Crassostrea gigas to environmental changes in Stansbury, South Australia from September 2005 to October 2006. A total of 360 oysters were grown in one-line baskets on the farm using six replicates that were sampled monthly. A range of environmental parameters were assessed and correlated against biological indicators for oyster condition, metabolism and antimicrobial activity. Food availability by chlorophyll a, was low throughout the study period (0.5–1.5 µg L? 1) and was significantly correlated to phosphorus concentrations. The condition index and shell weight of oysters significantly increased over the year, with the condition index dropping after spawning but then recovering within one month. Significant temporal variation in energy storage and utilization were observed in different tissues over the year. Glycogen in the mantle tissue was influenced by reproduction and correlated to chlorophyll a levels, but not in the gill or adductor muscle. The mantle glycogen and gill protein reached the lowest level in February when spawning occurred and presented evidence for seasonal variation in oyster metabolic activity. However, mantle and adductor muscle proteins did not drop after spawning indicating that these proteins contribute little to gametogenesis. Hemolymph protein was negatively correlated to water temperature and chlorophyll a, reaching the lowest level during summer. Hemolymph antibacterial activity significantly decreased after spawning, implying that the period of post-spawning is critical for oyster health. This study revealed trade-offs in the energy budget between immune resistance, growth, and reproduction. The results indicate that in a lean water environment, spawning events significantly regulate metabolic and immune capacities of oysters and a second year of rearing increased meat and shell weight but not the shell length. These findings are applicable to the management and development of oyster aquaculture within temperate southern hemisphere.
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