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Abstract Coral bleaching is the largest global threat to coral reef ecosystem persistence this century. Advancing our understanding of coral bleaching and developing solutions to protect corals and the reefs they support are critical. In the present article, we, the US National Science Foundation–funded Coral Bleaching Research Coordination Network, outline future directions for coral bleaching research. Specifically, we address the need for embedded inclusiveness, codevelopment, and capacity building as a foundation for excellence in coral bleaching research and the critical role of coral-bleaching science in shaping policy. We outline a path for research innovation and technology and propose the formation of an international coral bleaching consortium that, in coordination with existing multinational organizations, could be a hub for planning, coordinating, and integrating global-scale coral bleaching research, innovation, and mitigation strategies. This proposed strategy for future coral bleaching research could facilitate a step-function change in how we address the coral bleaching crisis. 

Abstract Globally, species are migrating in an attempt to track optimal isotherms as climate change increasingly warms existing habitats. Stony corals are severely threatened by anthropogenic warming, which has resulted in repeated mass bleaching and mortality events. Since corals are sessile as adults and with a relatively old age of sexual maturity, they are slow to latitudinally migrate, but corals may also migrate vertically to deeper, cooler reefs. Herein we describe vertical migration of the Mediterranean coral Oculina patagonica from less than 10 m depth to > 30 m. We suggest that this range shift is a response to rapidly warming sea surface temperatures on the Israeli Mediterranean coastline. In contrast to the vast latitudinal distance required to track temperature change, this species has migrated deeper where summer water temperatures are up to 2 °C cooler. Comparisons of physiology, morphology, trophic position, symbiont type, and photochemistry between deep and shallow conspecifics revealed only a few depth-specific differences. At this study site, shallow colonies typically inhabit low light environments (caves, crevices) and have a facultative relationship with photosymbionts. We suggest that this existing phenotype aided colonization of the mesophotic zone. This observation highlights the potential for other marine species to vertically migrate. 

Evidence has shown that individually feeding or reduced light can mitigate the negative effects of elevated temperature on coral physiology. We aimed to evaluate if simultaneous low light and feeding would mitigate, minimize, or exacerbate negative effects of elevated temperature on coral physiology and carbon budgets. Pocillopora damicornis, Stylophora pistillata, and Turbinaria reniformis were grown for 28 days under a fully factorial experiment including two seawater temperatures (ambient temperature of 25 °C, elevated temperature of 30 °C), two light levels (high light of 300 μmol photons m−2 s−1, low light of 150 μmol photons m−2 s−1), and either fed (Artemia nauplii) or unfed. Coral physiology was significantly affected by temperature in all species, but the way in which low light and feeding altered their physiological responses was species-specific. All three species photo-acclimated to low light by increasing chlorophyll a. Pocillopora damicornis required feeding to meet metabolic demand irrespective of temperature but was unable to maintain calcification under low light when fed. In T. reniformis, low light mitigated the negative effect of elevated temperature on total lipids, while feeding mitigated the negative effects of elevated temperature on metabolic demand. In S. pistillata, low light compounded the negative effects of elevated temperature on metabolic demand, while feeding minimized this negative effect but was not sufficient to provide 100% metabolic demand. Overall, low light and feeding did not act synergistically, nor additively, to mitigate the negative effects of elevated temperature on P. damicornis, S. pistillata, or T. reniformis. However, feeding alone was critical to the maintenance of metabolic demand at elevated temperature, suggesting that sufficient supply of heterotrophic food sources is likely essential for corals during thermal stress (bleaching) events. 

Coral reefs are declining worldwide primarily because of bleaching and subsequent mortality resulting from thermal stress. Currently, extensive efforts to engage in more holistic research and restoration endeavors have considerably expanded the techniques applied to examine coral samples. Despite such advances, coral bleaching and restoration studies are often conducted within a specific disciplinary focus, where specimens are collected, preserved, and archived in ways that are not always conducive to further downstream analyses by specialists in other disciplines. This approach may prevent the full utilization of unexpended specimens, leading to siloed research, duplicative efforts, unnecessary loss of additional corals to research endeavors, and overall increased costs. A recent US National Science Foundation-sponsored workshop set out to consolidate our collective knowledge across the disciplines of Omics, Physiology, and Microscopy and Imaging regarding the methods used for coral sample collection, preservation, and archiving. Here, we highlight knowledge gaps and propose some simple steps for collecting, preserving, and archiving coral-bleaching specimens that can increase the impact of individual coral bleaching and restoration studies, as well as foster additional analyses and future discoveries through collaboration. Rapid freezing of samples in liquid nitrogen or placing at −80 °C to −20 °C is optimal for most Omics and Physiology studies with a few exceptions; however, freezing samples removes the potential for many Microscopy and Imaging-based analyses due to the alteration of tissue integrity during freezing. For Microscopy and Imaging, samples are best stored in aldehydes. The use of sterile gloves and receptacles during collection supports the downstream analysis of host-associated bacterial and viral communities which are particularly germane to disease and restoration efforts. Across all disciplines, the use of aseptic techniques during collection, preservation, and archiving maximizes the research potential of coral specimens and allows for the greatest number of possible downstream analyses.