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Acropora latistella. Specimen number: (A-C, E) VAM55; (D) VAM10. (A) live colony; (B, E) radial corallites; (C) branch fragment; (D) axial corallite. 

Acropora latistella. Specimen number: (A-C, E) VAM55; (D) VAM10. (A) live colony; (B, E) radial corallites; (C) branch fragment; (D) axial corallite. 

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... In between corallites, coenosteum is reticulate with elaborated spinules ( Figure 1C). They have compound coral colonies with bushy or table-like structures, with the branches appearing as finger-like projections from encrusting basal plates and share a similar growth form with Acropora humilis but a smaller branch diameter (1 cm versus 3 cm) (Sola et al., 2015). Rarely, they can be found in other growth forms. ...
... (A) Image of A. digitifera colony from Pulau Bidong with closed up image of photosynthetic Symbiodiniaceae family of algae (circle) that lives in the gastrodermal tissue of scleractinian corals. (B) The radial view and (C) side view of A. digitifera skeleton adopted fromSola et al. (2015). ...
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Coral responses to thermal stress remain inadequately understood in Southeast Asia, particularly in Malaysia. This study addresses this knowledge gap by investigating the influence of high temperatures on the scleractinian coral Acropora digitifera from Pulau Bidong through two parts: field surveys and manipulative experiments (i.e., control vs. exposure). In both parts, similar methodologies were applied, encompassing biochemical parameters (i.e., glutathione S-transferase activity, catalase activity, superoxide dismutase activity, malondialdehyde level, and thiol content) and bleaching evaluation through Symbiodiniaceae (SD) density. Furthermore, several samples from both parts were selected, and thiol-containing proteins were extracted and identified through proteomic analysis using mass spectrometry. In the field, despite a temperature increase in March 2020, SD density in A. digitifera was not affected, and this is due to gradual temperature changes, inadequate exposure duration, and potential environmental buffering. Besides, coral manages oxidative stress through physiological acclimatization, such as increasing or decreasing antioxidant enzyme activities. However, a higher SD density can likely increase oxidative pressure, as reflected by the negative correlation between SD density and thiol content, but no significant induction in antioxidant enzyme activity was evident. This was further demonstrated in an ex-situ experiment where A. digitifera experienced reduced thiol content when it was exposed to 31 °C at a higher rate of temperature increase. This highlights the importance of SD removal to release a certain amount of oxidative pressure and aligns with the thermotolerant nature of A. digitifera. This study hypothesizes coral may apply other oxidative regulation strategies, such as reversible oxidative modification through oxidoreductase activities. Proteomic analysis further corroborates its adaptive mechanisms under bleaching and thermal stress, including the absence of hyperoxidation indications and the presence of metabolic proteins. Furthermore, an increase in the number of proteins present in the endoplasmic reticulum (ER) influences folding activities and lumen components, highlighting the role of orchestrated oxidative protein regulation and potential ER stress. Overall, this study enhances our understanding of the thermotolerant characteristics of A. digitifera and reveals the potential adaptive approaches that may be applied by the coral to survive in high-temperature environments, providing valuable insights for coral conservation and climate change resilience.
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