食物浓度和光照强度对模式珊瑚生长的影响

Oceans Pub Date : 2024-03-25 DOI:10.3390/oceans5020009
Tung-Yung Fan, Yan-Leng Huang, Anderson Mayfield
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摘要

由于造礁珊瑚依靠异养和内共生甲藻自养来满足其新陈代谢的需要,因此在优化其原位培养时有必要分别考虑食物供应和光照水平。在这里,在光合有效辐射水平为 370 或 670 μmol quanta m-2 s-1 的循环水产养殖系统中养殖的模式礁珊瑚 Pocillopora acuta 的幼体,在一个单独的饲养箱中每周三次在黑暗中喂养浓度为 33 或 78 个 mL-1 的蒿甲藻稚虫 6 小时。在为期 84 天的实验开始时,对部分珊瑚进行了实验性损伤,以评估其恢复情况,结果发现 100%的珊瑚在 2-4 周内完全愈合。所有培养的珊瑚都存活了下来,未受伤的珊瑚(1)以每天接近 0.5% 的特定生长率生长,(2)表现出每天 0.2% 的平均总线性延伸率(每年约 6-8 厘米);这些都远远高于通常记录的原生境生长率。在饲养箱中,珊瑚对硝酸盐的耐受力最高可达 25 毫克/升,但当硝酸盐浓度在第 84 天达到 50 毫克/升时,其中一个饲养箱中的珊瑚开始出现组织坏死。这凸显了在珊瑚长期养殖过程中分池饲养的重要性,在未来的珊瑚养殖研究中,生物过滤可以减少有机物积累的可能性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of Food Concentration and Light Intensity on the Growth of a Model Coral
Since reef-building corals rely on both heterotrophy and endosymbiotic dinoflagellate autotrophy to meet their metabolic needs, it is necessary to consider both food supply and light levels, respectively, when optimizing their cultivation ex situ. Herein nubbins of the model reef coral Pocillopora acuta cultured in recirculating aquaculture systems at photosynthetically active radiation levels of 370 or 670 μmol quanta m−2 s−1 were fed Artemia nauplii at concentrations of either 33 or 78 individuals mL−1 in a separate feeding tank for 6 hr in the dark thrice weekly. A subset of nubbins was experimentally wounded at the outset of the 84-day experiment to assess recovery, and 100% fully healed within 2–4 weeks. All cultured corals survived, and unwounded corals (1) grew at a specific growth rate approaching 0.5% day−1 and (2) demonstrated a mean total linear extension of 0.2% day−1 (~6–8 cm year−1); these are far higher than growth rates normally documented in situ. In the feeding tank, corals tolerated nitrate levels up to 25 mg L−1, but once concentrations reached 50 mg L−1 by day 84, tissue necrosis began to occur in nubbins of one tank. This highlights the importance of feeding in separate tanks during long-term culture of corals, and bio-filtration could reduce the possibility of organic matter accumulation in future coral culture studies.
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