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鹿角珊瑚(Stylophora pistillata)中浮游动物摄食、光合作用与骨骼生长之间的相互作用。

Interactions between zooplankton feeding, photosynthesis and skeletal growth in the scleractinian coral Stylophora pistillata.

作者信息

Houlbrèque Fanny, Tambutté Eric, Allemand Denis, Ferrier-Pagès Christine

机构信息

Centre Scientifique de Monaco, Avenue Saint-Martin, MC-98000 Monaco (Principality).

出版信息

J Exp Biol. 2004 Apr;207(Pt 9):1461-9. doi: 10.1242/jeb.00911.

DOI:10.1242/jeb.00911
PMID:15037640
Abstract

We investigated the effect of zooplankton feeding on tissue and skeletal growth of the scleractinian coral Stylophora pistillata. Microcolonies were divided into two groups: starved corals (SC), which were not fed during the experiment, and fed corals (FC), which were abundantly fed with Artemia salina nauplii and freshly collected zooplankton. Changes in tissue growth, photosynthesis and calcification rates were measured after 3 and 8 weeks of incubation. Calcification is the deposition of both an organic matrix and a calcium carbonate layer, so we measured the effect of feeding on both these parameters, using incorporation of (14)C-aspartic acid and (45)Ca, respectively. Aspartic acid is one of the major components of the organic matrix in scleractinian corals. For both sampling times, protein concentrations were twice as high in FC than in SC (0.73 vs 0.42 mg P(-1) cm(-2) skeleton) and chlorophyll c(2) concentrations were 3-4 times higher in fed corals (2.1+/-0.3 micro g cm(-2)). Cell specific density (CSD), which corresponds to the number of algal cells inside a host cell, was also significantly higher in FC (1.416+/-0.028) than in SC (1.316+/-0.015). Fed corals therefore displayed a higher rate of photosynthesis per unit area (P(g)(max)= 570+/-60 nmol O(2) cm(-2) h(-1) and I(k)=403+/-27 micro mol photons m(-2) s(-1)). After 8 weeks, both light and dark calcification rates were twofold greater in FC (3323+/-508 and 416+/-58 nmol Ca(2+) 2 h(-1) g(-1) dry skeletal mass) compared to SC (1560+/-217 and 225+/-35 nmol Ca(2+) 2 h(-1) g(-1) dry skeletal mass, respectively, under light and dark conditions). Aspartic acid incorporation rates were also significantly higher in FC (10.44+/-0.69 and 1.36+/- 0.26%RAV 2 h(-1) g(-1) dry skeletal mass, where RAV is total radioactivity initially present in the external medium) than in SC (6.51+/-0.45 and 0.44+/-0.02%RAV 2 h(-1) g(-1) dry skeletal mass under dark and light conditions, respectively). Rates of dark aspartic acid incorporation were lower than the rates measured in the light. Our results suggest that the increase in the rates of calcification in fed corals might be induced by a feeding-stimulation of organic matrix synthesis.

摘要

我们研究了浮游动物摄食对石珊瑚类的皮氏角蜂巢珊瑚组织和骨骼生长的影响。微型珊瑚群体被分为两组:饥饿珊瑚(SC),在实验期间不进行投喂;投喂珊瑚(FC),大量投喂卤虫无节幼体和新采集的浮游动物。在培育3周和8周后,测量组织生长、光合作用和钙化速率的变化。钙化是有机基质和碳酸钙层的沉积,因此我们分别使用(14)C - 天冬氨酸和(45)Ca的掺入量来测量摄食对这两个参数的影响。天冬氨酸是石珊瑚类有机基质的主要成分之一。在两个采样时间点,投喂珊瑚中的蛋白质浓度均是饥饿珊瑚中的两倍(分别为0.73对0.42毫克磷(-1)平方厘米骨骼),投喂珊瑚中的叶绿素c2浓度高出3 - 4倍(2.1±0.3微克平方厘米(-2))。细胞比密度(CSD),即宿主细胞内藻类细胞的数量,在投喂珊瑚(1.416±0.028)中也显著高于饥饿珊瑚(1.316±0.015)。因此,投喂珊瑚每单位面积的光合作用速率更高(P(g)(max) = 570±60纳摩尔氧气平方厘米(-2)小时(-1)且I(k) = 403±27微摩尔光子平方米(-2)秒(-1))。8周后,与饥饿珊瑚相比,投喂珊瑚在光照和黑暗条件下的钙化速率均提高了两倍(分别为3323±508和416±58纳摩尔钙离子2小时(-1)克(-1)干骨骼质量)(饥饿珊瑚在光照和黑暗条件下分别为1560±217和225±35纳摩尔钙离子2小时(-1)克(-1)干骨骼质量)。天冬氨酸掺入率在投喂珊瑚中也显著高于饥饿珊瑚(分别为10.44±0.69和1.36±0.26%RAV 2小时(-1)克(-1)干骨骼质量,其中RAV是最初存在于外部介质中的总放射性)(饥饿珊瑚在黑暗和光照条件下分别为6.51±0.45和0.44±0.02%RAV 2小时(-1)克(-1)干骨骼质量)。黑暗中天冬氨酸掺入率低于光照下测量的速率。我们的结果表明,投喂珊瑚中钙化速率的增加可能是由有机基质合成的摄食刺激所诱导的。

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