1. Mixotrophic organisms can derive nutrition from both auto-and heterotrophy, which allows them to use a variety of trophic pathways to sustain their metabolic demands under variable conditions. Therefore, when facing environmental change, these organisms are expected to demonstrate an intrinsic ability to acclimatize through trophic plasticity.2. Scleractinian corals are ecologically important mixotrophs, but understanding their trophic plasticity has been impaired by an oversimplification towards inconsistent proxies of coral diet and overlooking intraspecific variability.3. Here, we applied a Bayesian analysis of carbon and nitrogen stable isotope data to determine the trophic niches of six common species of scleractinian corals and their associated endosymbionts, and combined it with an unsupervised machine learning algorithm to identify trophic behaviours and strategies.4. We found a variable amount of nutritional plasticity identified by different trophic behaviours within and between mixotrophic corals living under the same environmental conditions. Furthermore, we observed changes in trophic plasticity across environmental conditions. Corals from variable environments had larger host and endosymbiont niches than corals from stable environments. In addition, deeper corals had niches indicating a greater degree of heterotrophy than shallow corals. Collectively, corals exhibited distinct trophic strategies by promoting trophic niche differentiation along the mixotrophic continuum and conspecific individual colonies displayed high trophic variation. 5. Our results provide a foundation to understand how mixotrophic organisms may adjust their nutrition in response to ongoing global environmental change and the consequential modification of benthic assemblages.
Rationale The stable isotope analysis of carbon and nitrogen is a powerful tool in many ecological studies, but different sample treatments may affect stable isotope ratios and hamper comparisons among studies. The goal of this study was to determine whether treatments that are commonly used to prepare scleractinian coral samples for stable isotope analysis yield different δ15N and δ13C values, and to provide guidelines toward a standardised protocol. Methods The animal tissues and Symbiodiniaceae of two symbiotic scleractinian coral species (Stylophora pistillata and Porites lutea) were divided into subsamples to test the effects of the drying method, lipid extraction, acidification treatment and water washing. All the subsamples were analysed for their δ15N and δ13C values, using continuous flow elemental analyser/isotope ratio mass spectrometry. Results The drying method and lipid extraction treatment had no substantial effects on the δ15N and δ13C values of Symbiodiniaceae and animal tissues. Acid treatment did cause significant differences in δ13C values (mean differences ≤0.5‰, with individual samples becoming up to 2.0‰ more negative), whereas no ecologically significant differences were observed in δ15N values. Animal tissue δ13C values may vary depending on whether samples are washed or not. Conclusions To move towards a standardised protocol in coral research, we recommend using an available drying method (as they are equally acceptable) for the stable isotope analysis of scleractinian corals, examining the need for lipid extraction on a case‐by‐case basis, performing a direct acidification of Symbiodiniaceae and animal tissues, and avoiding washing animal tissue with distilled water.
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