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Abstract Active chlorophyllafluorometry is a well‐established tool for noninvasively diagnosing coral functional state, but has not yet been developed as a rapid phenotyping (functional screening) platform as for agriculture and forestry. Here, we present a proof‐of‐concept using Light‐Induced Fluorescence Transient‐Fast Repetition Rate fluorometry (LIFT‐FRRf) to identify coral photobiological‐based phenotypes in the context of rapidly scaling coral propagation practices on the northern Great Barrier Reef. For example, resolving light niche plasticity to inform transplantation, and identifying functionally diverse colonies to maximize stock selection. We first used optically diverse laboratory‐reared corals and coral endosymbiont (Symbiodiniaceae) isolates to develop a phenotyping approach integrating FRRf instantaneous kinetic parameters (light harvesting, electron turnover rates) and light‐dependent parameters (dynamic “quenching” terms, saturating light intensity [E_K]). Subsequent field‐based LIFT‐FRRf phenotyping of coral from a selective (2‐4 m depth) reef habitat revealed that widely topographically dispersed platingAcroporataxa exhibited broad light niche plasticity (E_Kvariance) underpinned by multiple phenotypes that were predominantly differentiated by minimum electron turnover capacity; fluorometer configurations that cannot resolve kinetic parameters will thus likely have more limited capacity to resolve phenotypes. As such, platingAcroporahave broad propagation potential in terms of multiple functional variants for stock and across diverse light environments (growth, transplantation). In contrast, coral taxa (Pocillopora verrucosa,Echinopora lamellosa) with relatively restricted topographic dispersion exhibited less light niche plasticity and only single phenotypes, thereby imposing more constraints for propagation. We discuss the core technical, operational, and conceptual steps required to develop more sophisticated coral phenotyping platforms. 

Abstract The existence of widespread species with the capacity to endure diverse, or variable, environments are of importance to ecological and genetic research, and conservation. Such “ecological generalists” are more likely to have key adaptations that allow them to better tolerate the physiological challenges of rapid climate change. Reef‐building corals are dependent on endosymbiotic dinoflagellates (Family: Symbiodiniaceae) for their survival and growth. While these symbionts are biologically diverse, certain genetic types appear to have broad geographic distributions and are mutualistic with various host species from multiple genera and families in the order Scleractinia that must acquire their symbionts through horizontal transmission. Despite the considerable ecological importance of putative host‐generalist symbionts, they lack formal species descriptions. In this study, we used molecular, ecological, and morphological evidence to verify the existence of five new host‐generalist species in the symbiodiniacean genusCladocopium. Their geographic distribution and prevalence among host communities corresponds to prevailing environmental conditions at both regional and local scales. The influence that each species has on host physiology may partially explain regional differences in thermal sensitivities among coral communities. The potential increased prevalence of a generalist species that endures environmental instability is a consequential ecological response to warming oceans. Large‐scale shifts in symbiont dominance could ensure reef coral persistence and productivity in the near term. Ultimately, these formal designations should advance scientific communication and generate informed research questions on the physiology and ecology of coral‐dinoflagellate mutualisms. 

Within microeukaryotes, genetic variation and functional variation sometimes accumulate more quickly than morphological differences. To understand the evolutionary history and ecology of such lineages, it is key to examine diversity at multiple levels of organization. In the dinoflagellate family Symbiodiniaceae, which can form endosymbioses with cnidarians (e.g., corals, octocorals, sea anemones, jellyfish), other marine invertebrates (e.g., sponges, molluscs, flatworms), and protists (e.g., foraminifera), molecular data have been used extensively over the past three decades to describe phenotypes and to make evolutionary and ecological inferences. Despite advances in Symbiodiniaceae genomics, a lack of consensus among researchers with respect to interpreting genetic data has slowed progress in the field and acted as a barrier to reconciling observations. Here, we identify key challenges regarding the assessment and interpretation of Symbiodiniaceae genetic diversity across three levels: species, populations, and communities. We summarize areas of agreement and highlight techniques and approaches that are broadly accepted. In areas where debate remains, we identify unresolved issues and discuss technologies and approaches that can help to fill knowledge gaps related to genetic and phenotypic diversity. We also discuss ways to stimulate progress, in particular by fostering a more inclusive and collaborative research community. We hope that this perspective will inspire and accelerate coral reef science by serving as a resource to those designing experiments, publishing research, and applying for funding related to Symbiodiniaceae and their symbiotic partnerships.