Iluz David, Dubinsky Zvy
The Mina and Everard Goodman Faculty of Life Sciences, Bar-Ilan University, Geha Road, Ramat-Gan 5290002, Israel.
The Mina and Everard Goodman Faculty of Life Sciences, Bar-Ilan University, Geha Road, Ramat-Gan 5290002, Israel.
Zoology (Jena). 2015 Apr;118(2):71-8. doi: 10.1016/j.zool.2014.08.003. Epub 2014 Nov 3.
The relationship between reef-building corals and light-harvesting pigments of zooxanthellae (Symbiodinium sp.) has been acknowledged for decades. The photosynthetic activity of the algal endocellular symbionts may provide up to 90% of the energy needed for the coral holobiont. This relationship limits the bathymetric distribution of coral reefs to the upper 100 m of tropical shorelines. However, even corals growing under high light intensities have to supplement the photosynthates translocated from the algae by predation on nutrient-rich zooplankton. New information has revealed how the fate of carbon acquired through photosynthesis differs from that secured by predation, whose rates are controlled by light-induced tentacular extension. The Goreau paradigm of "light-enhanced calcification" is being reevaluated, based on evidence that blue light stimulates coral calcification independently from photosynthesis rates. Furthermore, under dim light, calcification rates were stoichiometrically uncoupled from photosynthesis. The rates of photosynthesis of the zooxanthellae exhibit a clear endogenous rhythmicity maintained by light patterns. This daily pattern is concomitant with a periodicity of all the antioxidant protective mechanisms that wax and wane to meet the concomitant fluctuation in oxygen evolution. The phases of the moon are involved in the triggering of coral reproduction and control the spectacular annual mass-spawning events taking place in several reefs. The intensity and directionality of the underwater light field affect the architecture of coral colonies, leading to an optimization of the exposure of the zooxanthellae to light. We present a summary of major gaps in our understanding of the relationship between light and corals as a roadmap for future research.
造礁珊瑚与虫黄藻(共生藻属)的光捕获色素之间的关系已被认可数十年。藻类细胞内共生体的光合作用活性可为珊瑚共生体提供高达90%所需能量。这种关系将珊瑚礁的水深分布限制在热带海岸线的上100米范围内。然而,即使是在高光强下生长的珊瑚,也必须通过捕食营养丰富的浮游动物来补充从藻类转运来的光合产物。新信息揭示了通过光合作用获取的碳的命运与通过捕食获得的碳的命运有何不同,捕食速率受光诱导的触手伸展控制。基于蓝光独立于光合作用速率刺激珊瑚钙化的证据,正在重新评估戈罗的“光增强钙化”范式。此外,在弱光条件下,钙化速率与光合作用在化学计量上解耦。虫黄藻的光合作用速率呈现出由光照模式维持的明显的内源性节律。这种每日模式与所有抗氧化保护机制的周期性相伴,这些机制会随着氧气释放的波动而增减。月相参与了珊瑚繁殖的触发,并控制着几个珊瑚礁中发生的壮观的年度大规模产卵事件。水下光场的强度和方向性影响珊瑚群落的结构,从而使虫黄藻对光的暴露达到最佳。我们总结了目前对光与珊瑚关系理解中的主要空白,作为未来研究的路线图。