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The shallow-water reef coral Goniastrea aspera Verill 1865 has previously been reported to demonstrate differences in within-colony susceptibility to bleaching at elevated sea temperatures; parts of the colony which are exposed to the highest solar radiation are more thermotolerant than areas which are less exposed. In this paper, we show that at elevated experimental sea temperature the 'high light' surfaces lose fewer symbiotic algae, have lower levels of oxidative stress, higher levels of host antioxidant-enzyme copper zinc superoxidase dismutase (CuZnSOD), and host heat-shock proteins 60 and 70, compared to the less exposed surfaces. In addition, 'high light' surfaces show less chronic photoinhibition and greater Photosystem II (PS II) recovery potential when exposed to high irradiance at ambient sea temperature. In contrast, no differences were noted in algal defences (e.g. antioxidant enzymes and stress protein production, and xanthophyll cycling) either at elevated or ambient temperatures. These results are noteworthy because they suggest that corals which acclimatise to high irradiance can, as a result, develop increased thermotolerance which may prevent bleaching at high sea temperatures. Importantly, they also demonstrate the significance of the host tissues in maintaining the intact symbiosis of G. aspera under thermal stress.

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Marked seasonality is observed in sea-surface temperature (SST) and photosynthetically active radiation (PAR) received by shallow water corals at Phuket, Thailand (7" N latitude). This seasonality is reflected in both algal densities and algal chlorophylls (a and C?) in 4 massive species of scleractinian corals, namely Coeloseris rnayeri, Goniastrea retiformis, Porites lutea, and G. aspera. Algal numbers and algal chlorophylls are generally maximal at the end of the wet season (November) and minimal at the end of the dry season (March to May). Algal densities are reduced by up to 53 % in May compared to November in some species, whde algal chlorophylls may be up to 4-fold greater in November. Concomitant with these changes are differences in algal cell volume in 3 out of the 4 species studied and alterations in host tissue depth, with smaller algal volume and greater tissue depth at the end of the wet compared with the dry season. Over the period 1993 to 1996 algal numbers showed a significant negative correlation with monthly (30 d) and short-term (1 to 2 d) values of both SST and PAR dose, while algal chlorophylls displayed a significant negative correlation with PAR dose in the 5 d preceding collection. Rising SST and increasing PAR in the dry season are paralleled by decreasing algal numbers and algal chlorophylls on an annual basis. Recovery of algal densities and a build-up in algal chlorophylls follow reductions in SST and PAR at the end of the wet season. In one of the years, when coral 'bleaching' was widespread at the study site (May 1995), the interaction between SST and PAR resulted in an 86 % reduction in algal densities in bleached corals compared to their annual maximum density. This study highlights the importance of seasonal fluctuations in physical environmental parameters and concomitant changes in the coravalgal symbiosis. Furthermore, it emphasises the need for greater understanding of the potential effects of seasonal and inter-annual variability on the status of algal symbionts, as well as identification of critical times of the year when visible bleaching may not be obvious but when algal numbers and algal chlorophylls are low and effects on coral physiology may be far-reaching.