Abstract

Photodamage of symbiotic algae exposed to thermal stress is involved in mass coral bleaching, a major cause of reef decline. Photoprotection is therefore a vital part of coral stress physiology. Corals produce a variety of green fluorescent protein (GFP)-like proteins from which some representatives screen the symbiotic algae from excess light. Different tissue concentrations of these GFP-like proteins distinguish colour morphs that are characteristic for many coral species. The question arises whether these pigmentation differences may diversify the niches that can be occupied by corals along the steep light gradient that structures coral reef communities. We assessed the implications of GFP-like protein expression in two color morphs of the symbiotic coral Hydnophora grandis, both associated with the same Symbiodinium sp. (subclade C40). The colour morphs of this species (high fluorescent, HF; and low fluorescent, LF), characterized by markedly different contents of a cyan fluorescent protein, were exposed to different quantities of blue light (470nm) that matched the major absorption band of the host pigment (473nm). High intensities of blue light caused less photodamage to the symbiotic algae of the HF morph and resulted in higher growth rates of these corals compared to representatives of the LF morph. In contrast, under low intensities of blue light, the HF morph showed lower growth rates than the LF morph, indicating that trade-offs are associated with high levels of fluorescent protein expression under this condition. Both morphs showed highest growth rates at medium light intensities with no obvious influence of the tissue pigmentation. Reef coral colour polymorphism caused by photoprotective GFP-like proteins may therefore be a product of balancing selection in which high pigment contents may be beneficial at the upper and detrimental at the lower end of the depth distribution range of symbiotic corals. Conversely, colour morphs with GFP-like proteins that function to optimize symbiont photosynthesis in low light environments could gain an advantage from the benefits offered by high pigment levels in deeper waters.

Highlights

  • Elevated sea water temperatures are a major cause of mass bleaching events and associated coral mortality (HoeghGuldberg, 1999; Hughes et al, 2017)

  • The sequences of the ITS2 region isolated from both color morphs under study matched those of Symbiodinium C40a and C40b (GenBank accession numbers AY589747 and AY589748), indicating that the symbiont complement of both color morphs is dominated by the same Symbiodinium sp

  • In colonies growing side by side under a photon flux of ∼250 μmol photons m−2s−1 of white light illumination prior to the start of the experiment, the cyan fluorescence of the high fluorescent (HF) morph was approximately ∼3.1-fold more intense compared to the low fluorescent (LF) morph (Figure 1A)

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Summary

Introduction

Elevated sea water temperatures are a major cause of mass bleaching events and associated coral mortality (HoeghGuldberg, 1999; Hughes et al, 2017). Corals and zooxanthellae have evolved protective mechanisms to reduce the impact of light stress In zooxanthellae, these mechanisms include: xanthophyll cycling (Ambarsari et al, 1997), the use of alternative electron pathways (Reynolds et al, 2008); and the downregulation of photosystem II reaction centers (Gorbunov et al, 2001). These mechanisms include: xanthophyll cycling (Ambarsari et al, 1997), the use of alternative electron pathways (Reynolds et al, 2008); and the downregulation of photosystem II reaction centers (Gorbunov et al, 2001) Both corals and zooxanthellae produce antioxidant enzymes (Lesser, 2006; Levy et al, 2006) and mycosporine-like amino acids (Banaszak et al, 2000; Shick, 2004; Starcevic et al, 2010) that help to protect the organisms from the negative impact of high light intensities

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