Growth and survival among Hawaiian corals outplanted from tanks to an ocean nursery are driven by individual genotype and species differences rather than preconditioning to thermal stress
Abstract:The drastic decline in coral coverage has stimulated an interest in reef restoration, and various iterations of coral nurseries have been used to augment restoration strategies. Here we examine the growth of two species of Hawaiian Montipora that were maintained in mesocosms under either ambient or warmed annual bleaching conditions for two consecutive years prior to outplanting to determine whether preconditioning aided coral restoration efforts. Using coral trees to create a nearby ocean nursery, we examined… Show more
“…To date, findings supporting the effect of environmental priming regimes on coral thermal tolerance are equivocal. While most studies indicate that a "challenging" thermal history or preconditioning regime (of thermal variability or elevated baseline temperature) enhances thermal tolerance of corals (McClanahan et al 2005;Bellantuono et al 2012b;Palumbi et al 2014;Buerger et al 2015;Schoepf et al 2015;Kenkel and Matz 2016;DeMerlis et al 2022;Brown et al 2023), some report neutral or negative results, including cases where corals ended up less stress resistant compared to the control group (Putnam and Edmunds 2011;Camp et al 2016;Schoepf et al 2019;Henley et al 2022). It has been suggested that such preconditioning treatments must have exerted too much stress on the corals with the consequence of having drained their energy reserves, hence did not contribute to stresshardening but rather had a contrary effect (Hackerott et al 2021;Wong et al 2021).…”
Section: Discussionmentioning
confidence: 99%
“…While many studies have reported positive effects of a variable environment on the stress tolerance in corals (Doering et al 2021;Oliver and Palumbi 2011b;Buerger et al 2015;Wong et al 2021;DeMerlis et al 2022;Brown et al 2023), a few have not reported any improvements or rather observed declines in stress tolerance. Negative reports are likely due to stress-buildup during the preconditioning process (Hackerott et al 2021), which can occur when a variability regime becomes too challenging (Putnam and Edmunds 2011;Camp et al 2016;Schoepf et al 2019;Klepac and Barshis 2020;Henley et al 2022). Also, dynamic interaction of all covariates present in the respective study sites can act as confounding factors and influence the outcomes of preconditioning (as laid out in the chapter above), but most importantly, the "priming dosage" will be decisive for the success of the method.…”
Section: Considerations For the Design Of Efficient Stress-hardening ...mentioning
Thermal variability can render corals stress resistant through a phenomenon coined as stress-hardening induced by environmental priming. Fluctuations that involve high temperature peaks have been commonly investigated, however, the effects of a stress-hardening stimulus generated by cold-water pulses has rarely been studied. Offshore island reefs in the Andaman Sea offer an ideal natural setting to study these effects, as cooling water of internal waves induce strong variability with peak intensity in January to June and absence in August to November. While western island shores are exposed to this stimulus, eastern shores remain sheltered. This study examined (1) whether corals from exposed reefs were more heat stress resistant compared to stimulus-sheltered conspecifics and (2) whether this trait can last in the absence of the stimulus. We quantified the thermal stress resistance in two ecologically important coral species, Pocillopora sp. and Porites sp., from the two island shores, during the two seasons. Coral bleaching intensity and photosynthetic efficiency of algal symbionts were measured as response variables after a short-term heat stress assay to assess thermal stress resistance. Stress responses of all stimulus-exposed corals were either undetectable (during the season of stimulus presence) or very weak (during stimulus absence), while corals from the stimulus-sheltered shore responded strongly to heat stress irrespective of the season. Hence, thermal resistance was overall greater in corals originating from the stimulus-exposed shore, but it was slightly diminished during the season of stimulus absence, emphasizing the relevance of stimulus recurrence in maintaining the resistance trait. We exemplify that the stimulus of fluctuating low temperature pulses successfully induced stress-hardening in corals. This suggests that priming stimuli do not necessarily need to transgress certain upper thermal thresholds, but can also touch on lower thresholds to be effective. Even more, we argue that cooling pulses might represent a safer stress-hardening regime, since warming-stress accumulation can be avoided. More research is required to obtain a better understanding of environmental priming, but current findings should encourage the development of artificial stress-hardening approaches to enhance coral resistance in reef restoration efforts.
“…To date, findings supporting the effect of environmental priming regimes on coral thermal tolerance are equivocal. While most studies indicate that a "challenging" thermal history or preconditioning regime (of thermal variability or elevated baseline temperature) enhances thermal tolerance of corals (McClanahan et al 2005;Bellantuono et al 2012b;Palumbi et al 2014;Buerger et al 2015;Schoepf et al 2015;Kenkel and Matz 2016;DeMerlis et al 2022;Brown et al 2023), some report neutral or negative results, including cases where corals ended up less stress resistant compared to the control group (Putnam and Edmunds 2011;Camp et al 2016;Schoepf et al 2019;Henley et al 2022). It has been suggested that such preconditioning treatments must have exerted too much stress on the corals with the consequence of having drained their energy reserves, hence did not contribute to stresshardening but rather had a contrary effect (Hackerott et al 2021;Wong et al 2021).…”
Section: Discussionmentioning
confidence: 99%
“…While many studies have reported positive effects of a variable environment on the stress tolerance in corals (Doering et al 2021;Oliver and Palumbi 2011b;Buerger et al 2015;Wong et al 2021;DeMerlis et al 2022;Brown et al 2023), a few have not reported any improvements or rather observed declines in stress tolerance. Negative reports are likely due to stress-buildup during the preconditioning process (Hackerott et al 2021), which can occur when a variability regime becomes too challenging (Putnam and Edmunds 2011;Camp et al 2016;Schoepf et al 2019;Klepac and Barshis 2020;Henley et al 2022). Also, dynamic interaction of all covariates present in the respective study sites can act as confounding factors and influence the outcomes of preconditioning (as laid out in the chapter above), but most importantly, the "priming dosage" will be decisive for the success of the method.…”
Section: Considerations For the Design Of Efficient Stress-hardening ...mentioning
Thermal variability can render corals stress resistant through a phenomenon coined as stress-hardening induced by environmental priming. Fluctuations that involve high temperature peaks have been commonly investigated, however, the effects of a stress-hardening stimulus generated by cold-water pulses has rarely been studied. Offshore island reefs in the Andaman Sea offer an ideal natural setting to study these effects, as cooling water of internal waves induce strong variability with peak intensity in January to June and absence in August to November. While western island shores are exposed to this stimulus, eastern shores remain sheltered. This study examined (1) whether corals from exposed reefs were more heat stress resistant compared to stimulus-sheltered conspecifics and (2) whether this trait can last in the absence of the stimulus. We quantified the thermal stress resistance in two ecologically important coral species, Pocillopora sp. and Porites sp., from the two island shores, during the two seasons. Coral bleaching intensity and photosynthetic efficiency of algal symbionts were measured as response variables after a short-term heat stress assay to assess thermal stress resistance. Stress responses of all stimulus-exposed corals were either undetectable (during the season of stimulus presence) or very weak (during stimulus absence), while corals from the stimulus-sheltered shore responded strongly to heat stress irrespective of the season. Hence, thermal resistance was overall greater in corals originating from the stimulus-exposed shore, but it was slightly diminished during the season of stimulus absence, emphasizing the relevance of stimulus recurrence in maintaining the resistance trait. We exemplify that the stimulus of fluctuating low temperature pulses successfully induced stress-hardening in corals. This suggests that priming stimuli do not necessarily need to transgress certain upper thermal thresholds, but can also touch on lower thresholds to be effective. Even more, we argue that cooling pulses might represent a safer stress-hardening regime, since warming-stress accumulation can be avoided. More research is required to obtain a better understanding of environmental priming, but current findings should encourage the development of artificial stress-hardening approaches to enhance coral resistance in reef restoration efforts.
“…Outplant sites can vary in their morphology (a at reef structure versus a spur and groove system) and the abiotic conditions they exhibit [27][28][29] . With different coral species exhibiting habitat preferences [30][31][32] , it is a key consideration for restoration. Additionally, within species variability also needs to be considered.…”
Coral reefs are experiencing decreases in coral cover due to anthropogenic influences. Coral restoration is addressing this decline by outplanting large volumes of corals onto reef systems. Understanding how outplanted corals react at a transcriptomic level to different outplant locations over time is important, as it will highlight how habitat affects the coral host and influences physiological measures. In this study, the transcriptomic dynamics of four genets of outplanted Acropora palmatawere assessed over a year at three reef sites in the Florida Keys. Genet identity was more important than time of sampling or outplant site, with differing levels of baseline immune and protein production the key drivers. Once accounting for genet, enriched growth processes were identified in the winter, and increased survival and immune expression were found in the summer. The effect of the reef site was small, with hypothesized differences in autotrophic versus heterotrophic dependent on outplant depth. We hypothesize that genotype identity is an important consideration for reef restoration, as differing baseline gene expression could play a role in survivorship and growth. Additionally, outplanting during cooler winter months may be beneficial due to higher expression of growth processes, allowing establishment of outplants on the reef system.
“…There are several possible contributing factors that may provide greater coral holobiont resilience to bleaching events: host-and/or symbiont-species (29)(30)(31)(32), host genotype (33)(34)(35)(36)(37)(38), or the microbial constituents of the holobiont's microbiome (39,40). At the center of this complex equation is the host's metabolic capacity before and after bleaching (i.e., how is the coral acquiring nutrients to sustain growth and immune function?).…”
Coral bleaching events from thermal stress are increasing globally in duration, frequency, and intensity. Bleaching occurs when a coral's algal symbionts are expelled, resulting in a loss of color. Some coral colonies survive bleaching, reacquire their symbionts and recover. In this study, we experimentally bleached Montipora capitata colonies to examine molecular and physiological signatures of intrinsic differences between corals that recover (resilient) compared to those that die (susceptible). All colonies were collected from the same bay and monitored for eight months post-bleaching to identify specific colonies exhibiting long-term resilience and survival. Using an integrated systems-biology approach that included quantitative mass spectrometry-based proteomics, 16S rRNA of the microbiome, total lipids, symbiont density and diversity, we explored molecular-level mechanisms of tolerance in pre- and post-bleached colonies and found biomarkers of resilience that can confidently identify resilient and susceptible corals before thermal-induced bleaching events. Prior to thermal stress, resilient corals were characterized by a more diverse microbiome and increased abundances of proteins involved in multiple carbon and nitrogen acquisition strategies, symbiont retention and acquisition, and pathogen resistance. Susceptible corals had early signs of symbiont rejection and had resorted to utilizing urea uptake pathways for carbon and nitrogen. Further, molecular signatures identified prior to bleaching were amplified after bleaching, suggesting these pathways may be deterministic in a colony's fate. Our results have important implications for the future of reefs, revealing molecular factors necessary for survival through thermally-induced bleaching events and providing diagnostic biomarkers for coral reef management.
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