1. Cornwall, C.E., S. Comeau, S.D. Donner, C. Perry, J. Dunne, R. van Hooidonk, S. Ryan, and C.A. Logan. Coral adaptive capacity insufficient to halt global transition of coral reefs into net erosion under climate change. Global Change Biology, 29(11):3010-3018, https://doi.org/10.1111/gcb.16647 2023

    Abstract:

    Projecting the effects of climate change on net reef calcium carbonate production is critical to understanding the future impacts on ecosystem function, but prior estimates have not included corals' natural adaptive capacity to such change. Here we estimate how the ability of symbionts to evolve tolerance to heat stress, or for coral hosts to shuffle to favourable symbionts, and their combination, may influence responses to the combined impacts of ocean warming and acidification under three representative concentration pathway (RCP) emissions scenarios (RCP2.6, RCP4.5 and RCP8.5). We show that symbiont evolution and shuffling, both individually and when combined, favours persistent positive net reef calcium carbonate production. However, our projections of future net calcium carbonate production (NCCP) under climate change vary both spatially and by RCP. For example, 19%–35% of modelled coral reefs are still projected to have net positive NCCP by 2050 if symbionts can evolve increased thermal tolerance, depending on the RCP. Without symbiont adaptive capacity, the number of coral reefs with positive NCCP drops to 9%–13% by 2050. Accounting for both symbiont evolution and shuffling, we project median positive NCCP of coral reefs will still occur under low greenhouse emissions (RCP2.6) in the Indian Ocean, and even under moderate emissions (RCP4.5) in the Pacific Ocean. However, adaptive capacity will be insufficient to halt the transition of coral reefs globally into erosion by 2050 under severe emissions scenarios (RCP8.5).

  2. Gove, J.M., J.A. Maynard, J. Lecky, D.P. Tracey, M.E. Allen, G.P. Asner, E. Conklin, C. Couch, K. Hum, R.J. Ingram, T.L. Kindinger, K. Leong, K.L.L. Oleson, E.K. Towle, R. van Hooidonk, G.J. Williams, and J. Hospital. 2022 ecosystem status report for Hawaiʻi. PIFSC Special Publication, SP-23-01, 91 pp., https://doi.org/10.25923/r53p-fn97 2023

    Abstract:

    No abstract.

  3. Johnson, J.E., D.J. Welch, R. van Hooidonk, D. Tracey, G. Chandrasa, B. Molinari, D. Triani, C. Tania, and H. Susanto. Climate change implications for the Arafura and Timor Seas region: Assessing vulnerability of marine systems to inform management and conservation. Climatic Change, 176:88, https://doi.org/10.1007/s10584-023-03554-9 2023

    Abstract:

    The Arafura and Timor Seas region is shared by Indonesia, Timor Leste, Australia, and Papua New Guinea (PNG), and is at the intersection of the Pacific and Indian oceans. High coastal population densities, degraded habitats, overexploited fisheries, low profile coasts, shallow continental shelves and macro-tidal conditions mean that coastal and marine environments in the region are currently facing multiple pressures. Climate change is expected to exacerbate these pressures and have profound effects on the status and distribution of coastal and marine habitats, the fish and invertebrates they support and, therefore, dependent communities and industries. Downscaled climate change projections for 2041–2070 for air and sea temperature, ocean chemistry and rainfall were modelled to provide spatially relevant regional data for a structured semi-quantitative vulnerability assessment. Results of the assessment were spatially variable and identified shallow coral reefs as highly vulnerable, particularly in the Timor-Leste and Indonesia-Arafura sub-regions. Seagrass meadows were most vulnerable in the Gulf of Carpentaria, Indonesia-Arafura, and Timor-Leste sub-regions. Mangrove habitats were most vulnerable in Timor-Leste and Western PNG sub-regions. Drivers of vulnerability include poor habitat condition, non-climate pressures, low connectivity, and limited formal management. Marine species vulnerability was also spatially variable, with highly vulnerable and priority species identified for each sub-region, including finfish and marine invertebrates. A key driver of species vulnerability was their stock status, with many species in Timor-Leste, Western PNG and Indonesia, and several in northern Australia, overfished or potentially overfished. Limited management in some sub-regions, as well as non-climate pressures such as habitat decline, poor water quality and illegal, unregulated and unreported fishing were also key drivers. Species of conservation interest (dugong and marine turtles) were also highly vulnerable to climate change, driven by their threatened status and the fact that they are low productivity species that take years to recover from impacts. Priority species and habitats for local action were identified and current pressures that undermine condition and/or resilience, with strategic recommendations aimed at minimising climate change vulnerability.

  4. Palacio-Castro, A.M., T.B. Smith, G.A. Snyder, V. Brandtneris, R. van Hooidonk, J.L. Maté, D. Manzello, P.W. Glynn, P. Fong, and A.C. Baker. Increased dominance of heat-tolerant symbionts create resilient coral reefs in near-term ocean warming. Proceedings of the National Academy of Science, 120(8):e2202388120, https://www.pnas.org/doi/10.1073/pnas.2202388120 2023

    Abstract:

    Climate change is radically altering coral reef ecosystems, mainly through increasingly frequent and severe bleaching events. Yet, some reefs have exhibited higher thermal tolerance after bleaching severely the first time. To understand changes in thermal tolerance in the eastern tropical Pacific (ETP), we compiled four decades of temperature, coral cover, coral bleaching, and mortality data, including three mass bleaching events during the 1982 to 1983, 1997 to 1998 and 2015 to 2016 El Niño heatwaves. Higher heat resistance in later bleaching events was detected in the dominant framework-building genus, Pocillopora, while other coral taxa exhibited similar susceptibility across events. Genetic analyses of Pocillopora spp. colonies and their algal symbionts (2014 to 2016) revealed that one of two Pocillopora lineages present in the region (Pocillopora “type 1”) increased its association with thermotolerant algal symbionts (Durusdinium glynnii) during the 2015 to 2016 heat stress event. This lineage experienced lower bleaching and mortality compared with Pocillopora “type 3”, which did not acquire D. glynnii. Under projected thermal stress, ETP reefs may be able to preserve high coral cover through the 2060s or later, mainly composed of Pocillopora colonies that associate with D. glynnii. However, although the low-diversity, high-cover reefs of the ETP could illustrate a potential functional state for some future reefs, this state may only be temporary unless global greenhouse gas emissions and resultant global warming are curtailed.

  5. Webb, A.E., I.C. Enochs, R. van Hooidonk, R.M. van Westen, N. Besemer, G. Kolodziej, T.S. Viehman, and D. Manzello. Restoration and coral adaptation delay, but do not prevent, climate-driven reef framework erosion of an inshore site in the Florida Keys. Scientific Reports, 13:258, https://doi.org/10.1038/s41598-022-26930-4 2023

    Abstract:

    For reef framework to persist, calcium carbonate production by corals and other calcifiers needs to outpace loss due to physical, chemical, and biological erosion. This balance is both delicate and dynamic and is currently threatened by the effects of ocean warming and acidification. Although the protection and recovery of ecosystem functions are at the center of most restoration and conservation programs, decision makers are limited by the lack of predictive tools to forecast habitat persistence under different emission scenarios. To address this, we developed a modeling approach, based on carbonate budgets, that ties species-specific responses to site-specific global change using the latest generation of climate models projections (CMIP6). We applied this model to Cheeca Rocks, an outlier in the Florida Keys in terms of high coral cover, and explored the outcomes of restoration targets scheduled in the coming 20 years at this site by the Mission: Iconic Reefs restoration initiative. Additionally, we examined the potential effects of coral thermal adaptation by increasing the bleaching threshold by 0.25, 0.5, 1 and 2˚C. Regardless of coral adaptative capacity or restoration, net carbonate production at Cheeca Rocks declines heavily once the threshold for the onset of annual severe bleaching is reached. The switch from net accretion to net erosion, however, is significantly delayed by mitigation and adaptation. The maintenance of framework accretion until 2100 and beyond is possible under a decreased emission scenario coupled with thermal adaptation above 0.5˚C. Although restoration initiatives increase reef accretion estimates, Cheeca Rocks will only be able to keep pace with future sea-level rise in a world where anthropogenic CO2 emissions are reduced. Present results, however, attest to the potential of restoration interventions combined with increases in coral thermal tolerance to delay the onset of mass bleaching mortalities, possibly in time for a low-carbon economy to be implemented and complementary mitigation measures to become effective.

  6. Holstein, D.M., T.B. Smith, R. van Hooidonk, and C.B. Paris. Predicting coral metapopulation decline in a changing thermal environment. Coral Reefs, 41(4):961-972, https://doi.org/10.1007/s00338-022-02252-9 2022

    Abstract:

    Thermal stress is expected to compromise the persistence of tropical corals throughout their biogeographic ranges, making many reefs inhospitable to corals by the end of the century. We integrated models of local predictions of thermal stress throughout the coming century, coral larval dispersal, and the persistence of a coral’s metapopulation(s) in the Caribbean to investigate broad trends in metapopulation fragmentation and decline. As coral reef patches become inhospitable throughout the next century, the metapopulation of Orbicella annularis is predicted to fragment, with sub-networks centered around highly connected patches and thermal refuges. Some of these are predicted to include the reefs of Colombia, Panama, Honduras, Guatemala, Belize, Southern and Northern Cuba, Haiti, and the Bahamas. Unknown coral population demographic parameters, such as lifetime egg production and stock-recruitment rates, limit the model’s predictions; however, a sensitivity analysis demonstrates that broadscale patterns of fragmentation and metapopulation collapse before the end of the century are consistent across a range of potential parameterizations. Despite dire predictions, the model highlights the potential value in protecting and restoring coral populations at strategic locations that are highly connected and/or influential to persistence. Coordinated conservation activities that support local resilience at low coral cover have the potential to stave off metapopulation collapse for decades, buying valuable time. Thermal refuges are linchpins of metapopulation persistence during moderate thermal stress, and targeted conservation or restoration that supports connectivity between these refuges by enhancing local population growth or sexual propagation may be critically important to species conservation on coral reefs.

  7. Humanes, A., L. Lachs, E.A. Beauchamp, J.C. Bythell, A.J. Edwards, Y. Golbuu, H.M. Martinez, P. Palmowski, A. Treumann, E. van der Steeg, R. van Hooidonk, and J.R. Guest. Within-population variability in coral heat tolerance indicates climate adaptation potential. Proceedings of the Royal Society B, 289(1981):20220872, https://doi.org/10.1098/rspb.2022.0872 2022

    Abstract:

    Coral reefs are facing unprecedented mass bleaching and mortality events due to marine heatwaves and climate change. To avoid extirpation, corals must adapt. Individual variation in heat tolerance and its heritability underpin the potential for coral adaptation. However, the magnitude of heat tolerance variability within coral populations is largely unresolved. We address this knowledge gap by exposing corals from a single reef to an experimental marine heatwave. We found that double the heat stress dosage was required to induce bleaching in the most-tolerant 10%, compared to the least-tolerant 10% of the population. By the end of the heat stress exposure, all of the least-tolerant corals were dead, whereas the most-tolerant remained alive. To contextualize the scale of this result over the coming century, we show that under an ambitious future emissions scenario, such differences in coral heat tolerance thresholds equate to up to 17 years delay until the onset of annual bleaching and mortality conditions. However, this delay is limited to only 10 years under a high emissions scenario. Our results show substantial variability in coral heat tolerance which suggests scope for natural or assisted evolution to limit the impacts of climate change in the short-term. For coral reefs to persist through the coming century, coral adaptation must keep pace with ocean warming, and ambitious emissions reductions must be realized.

  8. Obura, D., M. Gudka, M. Samoilys, K. Osuka, J. Mbugua, D.A. Keith, S. Porter, R. Roche, R. van Hooidonk, S. Ahamada, A. Araman, J. Karisa, J. Komakoma, M. Madi, I. Ravinia, H. Razafindrainibe, S. Yahya, and F. Zivane. Vulnerability to collapse of coral reef ecosystems in the western Indian Ocean. Nature Sustainability, 5(2):104-113, https://doi.org/10.1038/s41893-021-00817-0 2022

    Abstract:

    Ecosystems worldwide are under increasing threat. We applied a standardized method for assessing the risk of ecosystem collapse, the International Union for Conservation of Nature (IUCN) Red List of Ecosystems, to coral reefs in the Western Indian Ocean (WIO), covering 11,919 km2 of reef (~5% of the global total). Our approach combined indicators of change in historic ecosystem extent, ecosystem functioning (hard corals, fleshy algae, herbivores and piscivores) and projected sea temperature warming. We show that WIO coral reefs are vulnerable to collapse at the regional level, while in 11 nested ecoregions they range from critically endangered (islands, driven by future warming) to vulnerable (continental coast and northern Seychelles, driven principally by fishing pressure). Responses to avoid coral reef collapse must include ecosystem-based management of reefs and adjacent systems combined with mitigating and adapting to climate change. Our approach can be replicated across coral reefs globally to help countries and other actors meet conservation and sustainability targets set under multiple global conventions—including the Convention on Biological Diversity’s post-2020 global biodiversity framework and the United Nations’ Sustainable Development Goals. 

  9. Cornwall, C.E., S. Comeau, N.A. Kornder, C.T. Perry, R. van Hooidonk, T. DeCarlo, M.S. Pratchett, K. Anderson, N. Browne, R.C. Carpenter, G. Diaz-Pulido, J.P. D’Olivo, S.S. Doo, J. Figueiredo, S.A.V. Fortunato, E. Kennedy, C.A. Lantz, M. McCulloch, M. Gonzalez-Rivero, V. Schoepf, S. Smithers, and R.J. Lowe. Global declines in coral reef calcium carbonate production under ocean acidification and warming. Proceedings of the National Academy of Science, 118(21):e2015265118, https://doi.org/10.1073/pnas.2015265118 2021

    Abstract:

    Ocean warming and acidification threaten the future growth of coral reefs. This is because the calcifying coral reef taxa that construct the calcium carbonate frameworks and cement the reef together are highly sensitive to ocean warming and acidification. However, the global-scale effects of ocean warming and acidification on rates of coral reef net carbonate production remain poorly constrained despite a wealth of studies assessing their effects on the calcification of individual organisms. Here, we present global estimates of projected future changes in coral reef net carbonate production under ocean warming and acidification. We apply a meta-analysis of responses of coral reef taxa calcification and bioerosion rates to predicted changes in coral cover driven by climate change to estimate the net carbonate production rates of 183 reefs worldwide by 2050 and 2100. We forecast mean global reef net carbonate production under representative concentration pathways (RCP) 2.6, 4.5, and 8.5 will decline by 76, 149, and 156%, respectively, by 2100. While 63% of reefs are projected to continue to accrete by 2100 under RCP2.6, 94% will be eroding by 2050 under RCP8.5, and no reefs will continue to accrete at rates matching projected sea level rise under RCP4.5 or 8.5 by 2100. Projected reduced coral cover due to bleaching events predominately drives these declines rather than the direct physiological impacts of ocean warming and acidification on calcification or bioerosion. Presently degraded reefs were also more sensitive in our analysis. These findings highlight the low likelihood that the world's coral reefs will maintain their functional roles without near-term stabilization of atmospheric CO2 emissions.

  10. Cunning, R., K.E. Parker, K. Johnson-Sapp, R.F. Karp, A.D. Wen, O.M. Williamson, E. Bartels, M. D’Alessandro, D.S. Gilliam, G. Hanson, J. Levy, D. Lirman, K. Maxwell, W.C. Million, A.L. Moulding, A. Moura, E.M. Muller, K. Nedimyer, B. Reckenbeil, R. van Hooidonk, C. Dahlgren, C. Kenkel, J.E. Parkinson, and A.C. Baker. Census of heat tolerance among Florida’s threatened staghorn corals finds resilient individuals throughout existing nursery populations. Proceedings of the Royal Society B, 288(1961):20211613, https://doi.org/10.1098/rspb.2021.1613 2021

    Abstract:

    The rapid loss of reef-building corals due to ocean warming is driving the development of interventions such as coral propagation and restoration, selective breeding, and assisted gene flow. Many of these interventions target naturally heat-tolerant individuals to boost climate resilience, but the challenges of quickly and reliably quantifying heat tolerance and identifying thermotolerant individuals have hampered implementation. Here, we used coral bleaching automated stress systems to perform rapid, standardized heat tolerance assays on 229 colonies of Acropora cervicornis across six coral nurseries spanning Florida’s Coral Reef Tract, USA. Analysis of heat stress dose–response curves for each colony revealed a broad range in thermal tolerance among individuals (approximately 2.5°C range in Fv/Fm ED50), with highly reproducible rankings across independent tests (r = 0.76). Most phenotypic variation occurred within nurseries rather than between them, pointing to a potentially dominant role of fixed genetic effects in setting thermal tolerance and widespread distribution of tolerant individuals throughout the population. The identification of tolerant individuals provides immediately actionable information to optimize nursery and restor ation programmes for Florida’s threatened staghorn corals. This work further provides a blueprint for future efforts to identify and source thermally tolerant corals for conservation interventions worldwide.  KEY WORDS: Coral, coral reef, restoration, bleaching, climate change, thermal stress. 

  11. Kaufman, M.L., E. Watkins, R. van Hooidonk, A.C. Baker, and D. Lirman. Thermal history influences lesion recovery of the threatened Caribbean staghorn coral Acropora cervicornis under heat stress. Coral Reefs, 40(2):289-293, https://doi.org/10.1007/s00338-020-02025-2 2021

    Abstract:

    Anthropogenic climate change is the biggest threat to coral reefs, but reef restoration efforts are buying time for these ecosystems. Lesion recovery, which can be a determinant of colony survival, is particularly important for restored species. Here, we evaluate lesion recovery of 18 genets of Acropora cervicornis from Florida reefs with different thermal regimes in a temperature challenge experiment. Genets demonstrated significant variability in healing, which greatly slowed under heat stress. Only 35% of fragments healed at 31.5°C compared to 99% at 28°C. Donor reef thermal regime significantly influenced lesion recovery under heat stress with corals from warmer reefs demonstrating greater healing than corals from cooler reefs, but did not influence recovery under ambient conditions. These findings should encourage practitioners to utilize rapidly healing genets, avoid fragmentation in high temperatures, and incorporate assisted relocation by moving corals from warmer to cooler reefs, where they might succeed under future climate conditions.

  12. Storlazzi, C.D., O.M. Cheriton, R. van Hooidonk, Z. Zhao, and R. Brainard. Internal tides can provide thermal refugia that will buffer some coral reefs from future global warming. Scientific Reports, 10:13435, https://doi.org/ 10.1038/s41598-020-70372-9 2020

    Abstract:

    Observations show ocean temperatures are rising due to climate change, resulting in a fivefold increase in the incidence of regional-scale coral bleaching events since the 1980s. Analyses based on global climate models forecast bleaching will become an annual event for most of the world’s coral reefs within 30–50 yr. Internal waves at tidal frequencies can regularly flush reefs with cooler waters, buffering the thermal stress from rising sea-surface temperatures. Here we present the first global maps of the effects these processes have on bleaching projections for three IPCC-AR5 emissions scenarios. Incorporating semidiurnal temperature fluctuations into the projected water temperatures at depth creates a delay in the timing of annual severe bleaching ≥ 10 yr (≥ 20 yr) for 38% (9%), 15% (1%), and 1% (0%) of coral reef sites for the low, moderate, and high emission scenarios, respectively; regional averages can reach twice as high. These cooling effects are greatest later in twenty-first century for the moderate emission scenarios, and around the middle twenty-first century for the highest emission scenario. Our results demonstrate how these effects could delay bleaching for corals, providing thermal refugia. Identification of such areas could be a factor for the selection of coral reef marine protected areas.

  13. van Hooidonk, R., J. Maynard, G. Grimsditch, G. Williams, J. Tamelander, J. Gove, H. Koldewey, G. Ahmadia, D. Tracey, K. Hum, E. Conklin, and M. Berumen. Projections of future coral bleaching conditions using IPCC CMIP6 models: Climate policy implications, management applications, and regional seas summaries. United Nations Environment Programme, Nairobi, Kenya, 104 pp., 2020

    Abstract:

    No abstract.

  14. van, Hooidonk, R.J. Decision support tool to promote long-term survival of Acropora cervicornis on the Florida reef tract. NOAA Technical Report, OAR-AOML-53, 6 pp., https://doi.org/10.25923/cnz0-wp70 2020

    Abstract:

    To maximize the long-term survival (>10 years) of nursery raised Acropora cervicornis corals, a map-based tool was created that ranks locations in the Florida Acropora Critical Habitat based on climate vulnerability. Climate vulnerability is defined both in terms of exposure to future heat stress and the coral’s sensitivity as resilience. Suitable sites are determined by a number of factors. Suitable sites must also be within the Acropora Critical Habitat and within the depth range of 5-15 meters, with either hard bottom or coral present. These possible locations are ranked based on projected climate change impacts and a resilience metric based on seven different indicators. These rankings are intended to guide managers of nurseries to outplant locations on a coarser scale. However, where to outplant in these regions should still be determined by the local, small-scale conditions at the substrate.

  15. Asaad, I., C.J. Lundquist, M.V. Erdmann, R. van Hooidonk, and M.J. Costello. Designating spatial priorities for marine biodiversity conservation in the Coral Triangle. Frontiers in Marine Science, 5:400, https://doi.org/10.3389/fmars.2018.00400 2018

    Abstract:

    To date, most Marine Protected Areas (MPA) have been designated on an ad hoc basis. However, a comprehensive regional and global network should be designed to be representative of all aspects of biodiversity, including populations, species, and biogenic habitats. A good exemplar would be the Coral Triangle (CT) because it is the most species rich area in the ocean but only 2% of its area is in any kind of MPA. Our analysis consisted of five different groups of layers of biodiversity features: biogenic habitat, species richness, species of special conservation concern, restricted range species, and areas of importance for sea turtles. We utilized the systematic conservation planning software Zonation as a decision-support tool to ensure representation of biodiversity features while balancing selection of protected areas based on the likelihood of threats. Our results indicated that the average representation of biodiversity features within the existing MPA system is currently about 5%. By systematically increasing MPA coverage to 10% of the total area of the CT, the average representation of biodiversity features within the MPA system would increase to over 37%. Marine areas in the Halmahera Sea, the outer island arc of the Banda Sea, the Sulu Archipelago, the Bismarck Archipelago, and the Malaita Islands were identified as priority areas for the designation of new MPAs. Moreover, we recommended that several existing MPAs be expanded to cover additional biodiversity features within their adjacent areas, including MPAs in Indonesia (e.g., in the Birds Head of Papua), the Philippines (e.g., in the northwestern part of the Sibuyan Sea), Malaysia (e.g., in the northern part of Sabah), Papua New Guinea (e.g., in the Milne Bay Province), and the Solomon Islands (e.g., around Santa Isabel Island). An MPA system that covered 30% of the CT would include 65% of the biodiversity features. That just two-thirds of biodiversity was represented by one-third of the study area supports calls for at least 30% of the ocean to be in no-fishing MPA. This assessment provides a blueprint for efficient gains in marine conservation through the extension of the current MPA system in the Coral Triangle region.

  16. Bruno, J.F., A.E. Bates, C. Cacciapaglia, E.P. Pike, S.C. Amstrup, R. van Hooidonk, S.A. Henson, and R.B. Aronson. Climate change threatens the world’s marine protected areas. Nature Climate Change, 8(6):499-503, https://doi.org/10.1038/s41558-018-0149-2 2018

    Abstract:

    Marine protected areas (MPAs) are a primary management tool for mitigating threats to marine biodiversity. MPAs and the species they protect, however, are increasingly being impacted by climate change. Here we show that, despite local protections, the warming associated with continued business-as-usual emissions (RCP8.5) will likely result in further habitat and species losses throughout low-latitude and tropical MPAs. With continued business-as-usual emissions, mean sea-surface temperatures within MPAs are projected to increase 0.035°C per year and warm an additional 2.8°C by 2100. Under these conditions, the time of emergence (the year when sea-surface temperature and oxygen concentration exceed natural variability) is mid-century in 42% of 309 no-take marine reserves. Moreover, projected warming rates and the existing “community thermal safety margin” (the inherent buffer against warming based on the thermal sensitivity of constituent species) both vary among ecoregions and with latitude. The community thermal safety margin will be exceeded by 2050 in the tropics and by 2150 for many higher latitude MPAs. Importantly, the spatial distribution of emergence is stressor-specific. Hence, rearranging MPAs to minimize exposure to one stressor could well increase exposure to another. Continued business-as-usual emissions will likely disrupt many marine ecosystems, reducing the benefits of MPAs.

  17. Heron, S.F., R. van Hooidonk, J. Maynard, K. Anderson, J.C. Day, E. Geiger, O. Hoegh-Guldberg, T. Hughes, P. Marshall, D. Obura, and C.M. Eakin. Impacts of climate change on world heritage coral reefs: Update to the First Global Scientific Assessment. UNESCO World Heritage Centre, Paris, 5 pp., 2018

    Abstract:

    No abstract.

  18. Heron, S.F., C.M. Eakin, F. Douvere, K. Anderson, J.C. Day, E. Geiger, O. Hoegh-Guldberg, R. van Hooidonk, T. Hughes, P. Marshall, and D. Obura. Impacts of climate change on world heritage coral reefs: A first global scientific assessment. UNESCO World Heritage Centre, 12 pp., 2017

    Abstract:

    No abstract.

  19. Maynard, J.A., P.A. Marshall, B. Parker, E. Mcleod, G. Ahmadia, R. van Hooidonk, S. Planes, G.J. Williams, L. Raymundo, R. Beeden, and J. Tamelander. A guide to assessing coral reef resilience for decision support. United Nations Environment Programme, Nairobi, Kenya, 44 pp., 2017

    Abstract:

    No abstract.

  20. Okazaki, R.R., E.K. Towle, R. van Hooidonk, C. Mor, R.N. Winter, A.M. Piggot, R. Cunning, A.C. Baker, J.S. Klaus, P.K. Swart, and C. Langdon. Species-specific responses to climate change and community composition determine future calcification rates of Florida Keys reefs. Global Change Biology, 23(3):1023-1035, https://doi.org/10.1111/gcb.13481 2017

    Abstract:

    Anthropogenic climate change compromises reef growth as a result of increasing temperatures and ocean acidification. Scleractinian corals vary in their sensitivity to these variables, suggesting species composition will influence how reef communities respond to future climate change. Because data are lacking for many species, most studies that model future reef growth rely on uniform scleractinian calcification sensitivities to temperature and ocean acidification. To address this knowledge gap, calcification of 12 common and understudied Caribbean coral species was measured for two months under crossed temperatures (27, 30.3°C) and CO2 partial pressures (pCO2) (400, 900, 1300 μatm). Mixed-effects models of calcification for each species were then used to project community-level scleractinian calcification using Florida Keys reef composition data and IPCC AR5 ensemble climate model data. Three of the four most abundant species, Orbicella faveolata, Montastraea cavernosa, and Porites astreoides, had negative calcification responses to both elevated temperature and pCO2. In the business-as-usual CO2 emissions scenario, reefs with high abundances of these species had projected end-of-century declines in scleractinian calcification of >50% relative to present-day rates. Siderastrea siderea, the other most common species, was insensitive to both temperature and pCO2 within the levels tested here. Reefs dominated by this species had the most stable end-of-century growth. Under more optimistic scenarios of reduced CO2 emissions, calcification rates throughout the Florida Keys declined <20% by 2100. Under the most extreme emissions scenario, projected declines were highly variable among reefs, ranging 10–100%. Without considering bleaching, reef growth will likely decline on most reefs, especially where resistant species like S. siderea are not already dominant. This study demonstrates how species composition influences reef community responses to climate change and how reduced CO2 emissions can limit future declines in reef calcification.

  21. van Hooidonk, R., J.A. Maynard, J. Tamelander, J. Gove, G. Ahmadia, L. Raymundo, G. Williams, S. Heron, D. Tracey, B. Parker, and S. Planes. Coral bleaching futures—downscaled projections of bleaching conditions for the world’s coral reefs, implications of climate policy and management responses. United Nations Environment Programme, Nairobi, Kenya, 68 pp., 2017

    Abstract:

    No abstract.

  22. Eisenlord, M.E., M.L. Groner, R.M. Yoshioka, J. Elliott, J. Maynard, S. Fradkin, M. Turner, K. Pyne, N. Rivlin, R. van Hooidonk, and C.D. Harvell. Ochre star mortality during the 2014 wasting disease epizootic: Role of population size structure and temperature. Philosophical Transactions of the Royal Society B, 371(1689):20150212, https://doi.org/10.1098/rstb.2015.0212 2016

    Abstract:

    Over 20 species of asteroids were devastated by a sea star wasting disease (SSWD) epizootic, linked to a densovirus, from Mexico to Alaska in 2013 and 2014. For Pisaster ochraceus from the San Juan Islands, South Puget Sound, and Washington outer coast, time-series monitoring showed rapid disease spread, high mortality rates in 2014, and continuing levels of wasting in the survivors in 2015. Peak prevalence of disease at 16 sites ranged to 100%, with an overall mean of 61%. Analysis of longitudinal data showed disease risk was correlated with both size and temperature and resulted in shifts in population size structure; adult populations fell to one quarter of pre-outbreak abundances. In laboratory experiments, time between development of disease signs and death was influenced by temperature in adults but not juveniles, and adult mortality was 18% higher in the 19°C treatment compared to the lower temperature treatments. While larger ochre stars developed disease signs sooner than juveniles, diseased juveniles died more quickly than diseased adults. Unusual 2-3°C warm temperature anomalies were coincident with the summer 2014 mortalities. We suggest these warm waters could have increased the disease progression and mortality rates of SSWD in Washington State.

  23. Heron, S.F., J.A. Maynard, R. van Hooidonk, and C.M. Eakin Warming trends and bleaching stress of the world’s coral reefs, 1985-2012. Nature Scientific Reports, 6:38402, https://doi.org/10.1038/srep38402 2016

    Abstract:

    Coral reefs across the world’s oceans are in the midst of the longest bleaching event on record (from 2014 to at least 2016). As many of the world’s reefs are remote, there is limited information on how past thermal conditions have influenced reef composition and current stress responses. Using satellite temperature data for 1985–2012, the analysis we present is the first to quantify, for global reef locations, spatial variations in warming trends, thermal stress events and temperature variability at reef-scale (~4 km). Among over 60,000 reef pixels globally, 97% show positive SST trends during the study period with 60% warming significantly. Annual trends exceeded summertime trends at most locations. This indicates that the period of summer-like temperatures has become longer through the record, with a corresponding shortening of the "winter" reprieve from warm temperatures. The frequency of bleaching-level thermal stress increased three-fold between 1985–91 and 2006–12 – a trend climate model projections suggest will continue. The thermal history data products developed enable needed studies relating thermal history to bleaching resistance and community composition. Such analyses can help identify reefs more resilient to thermal stress.

  24. Keith, S.A., J.A. Maynard, A.J. Edwards, J.R. Guest, A.G. Bauman, R. van Hooidonk, S.F. Heron, M.L. Berumen, J. Bouwmeester, S. Piromvaragorn, C. Rahbek, and A.H. Baird. Coral mass spawning predicted by rapid seasonal rise in ocean temperature. Proceedings of the Royal Society of London B, 283(1830):20160011, https://doi.org/10.1098/rspb.2016.0011 2016

    Abstract:

    Coral spawning times have been linked to multiple environmental factors; however, to what extent these factors act as generalized cues across multiple species and large spatial scales is unknown. We used a unique dataset of coral spawning from 34 reefs in the Indian and Pacific Oceans to test if month of spawning and peak spawning month in assemblages of Acropora spp. can be predicted by sea surface temperature (SST), photosynthetically available radiation, wind speed, current speed, rainfall, or sunset time. Contrary to the classic view that high mean SST initiates coral spawning, we found rapid increases in SST to be the best predictor in both cases (month of spawning: R2 = 0.73, peak: R2 = 0.62). Our findings suggest that a rapid increase in SST provides the dominant proximate cue for coral mass spawning over large geographical scales. We hypothesize that coral spawning is ultimately timed to ensure optimal fertilization success.

  25. Maynard, J., R. van Hooidonk, C.D. Harvell, C.M. Eakin, G. Liu, B.L. Willis, G.J. Williams, M. Groner, A. Dobson, S.F. Heron, R. Glenn, K. Reardon, and J.D. Shields. Improving marine disease surveillance through sea temperature monitoring, outlooks, and projections. Philosophical Transactions of the Royal Society B, 371(1689):20150208, https://doi.org/10.1098/rstb.2015.0208 2016

    Abstract:

    To forecast marine disease outbreaks as oceans warm requires new environmental surveillance tools. We describe an iterative process for developing these tools that combines research, development, and deployment for suitable systems. The first step is to identify candidate host-pathogen systems. The 24 candidate systems we identified include sponges, corals, oysters, crustaceans, sea stars, fishes, and sea grasses (among others). To illustrate the other steps, we present a case study of epizootic shell disease (ESD) in the American lobster. Increasing prevalence of ESD is a contributing factor to lobster fishery collapse in southern New England (SNE), raising concerns disease prevalence will increase in the northern Gulf of Maine under climate change. The lowest maximum bottom temperature associated with ESD prevalence in SNE is 12°C. Our seasonal outlook for 2015 and long-term projections shows bottom temperatures greater than or equal to 12°C may occur in this and coming years in the coastal bays of Maine. The tools presented will allow managers to target efforts to monitor the effects of ESD on fishery sustainability and will be iteratively refined. The approach and case example highlight that temperature-based surveillance tools can inform research, monitoring, and management of emerging and continuing marine disease threats.

  26. Maynard, J.A., R. Beeden, M. Puotinen, J.E. Johnson, P. Marshall, R. van Hooidonk, S.F. Heron, M. Devlin, E. Lawrey, J. Dryden, N. Ban, D. Wachenfeld, and S. Planes. Great Barrier Reef no-take areas include a range of disturbance regimes. Conservation Letters, 9(3):191-199, https://doi.org/10.1111/conl.12198 2016

    Abstract:

    Exposure to disturbance is rarely considered in marine protected area planning. Typically, representing and replicating the habitat types present within protected areas is used to spread the risk of protecting frequently disturbed sites. This was the approach used during the 2004 re-zoning of the Great Barrier Reef Marine Park (GBRMP) via the Representative Areas Program. Over 10 years later, we examine whether the risk was spread by mapping exposure of coral reefs in the GBRMP to four disturbances that cause coral mortality: bleaching, tropical cyclones, crown-of-thorns starfish outbreaks, and freshwater inundation. Our objectives were to: (1) assess whether no-take areas include a range of disturbance regimes; and (2) identify coral reef areas with lower relative exposure. At least 13% and an average of 31% of reef locations in each of 11 exposure classes are included within no-take areas. A greater proportion of low-exposure areas are within no-take areas than high-exposure areas (34.2% vs. 28.3%). The results demonstrate the value of risk spreading when exposure data are not available, while also showing that regularly assessing exposure increases capacity for adaptive, resilience-based reef management.

  27. Pendleton, L., A. Comte, C. Langdon, J.A. Ekstrom, S.R. Cooley, L. Suatoni, M.W. Beck, L.M. Brander, L. Burke, J.E. Cinner, C. Doherty, P.E.T. Edwards, D. Gledhill, L.-Q. Jiang, R.J. van Hooidonk, L. Teh, G.G. Waldbusser, and J. Ritter. Coral reefs and people in a high CO2 world: Where can science make a difference to people? PLoS ONE, 11(11):e0164699, https://doi.org/10.1371/journal.pone.0164699 2016

    Abstract:

    Increasing levels of carbon dioxide in the atmosphere put shallow, warm-water coral reef ecosystems, and the people who depend upon them, at risk from two key global environmental stresses: (1) elevated sea surface temperature (that can cause coral bleaching and related mortality); and (2) ocean acidification. These global stressors: cannot be avoided by local management; compound local stressors; and hasten the loss of ecosystem services. Impacts to people will be most grave where (a) human dependence on coral reef ecosystems is high, (b) sea surface temperature reaches critical levels soonest, and (c) ocean acidification levels are most severe. Where these elements align, swift action will be needed to protect people’s lives and livelihoods, but such action must be informed by data and science. Designing policies to offset potential harm to coral reef ecosystems and people requires a better understanding of where CO2-related global environmental stresses could cause the most severe impacts. Mapping indicators have been proposed as a way of combining natural and social science data to identify policy actions even when the needed science is relatively nascent. To identify where people are at risk and where more science is needed, we map indicators of biological, physical, and social science factors to understand how human dependence on coral reef ecosystems will be affected by globally-driven threats to corals expected in a high-CO2 world. Western Mexico, Micronesia, Indonesia, and parts of Australia have high human dependence and will likely face severe combined threats. As a region, southeast Asia is particularly at risk. Many of the countries most dependent upon coral reef ecosystems are places for which we have the least robust data on ocean acidification. These areas require new data and interdisciplinary scientific research to help coral reef-dependent human communities better prepare for a high CO2 world.

  28. van Hooidonk, R., J. Maynard, J. Tamelander, J. Gove, G. Ahmadia, L. Raymundo, G. Williams, S.F. Heron, and S. Planes. Local-scale projections of coral reef futures and implications of the Paris Agreement. Nature Scientific Reports, 6:39666, https://doi.org/10.1038/srep39666 2016

    Abstract:

    Increasingly frequent severe coral bleaching is among the greatest threats to coral reefs posed by climate change. Global climate models (GCMs) project great spatial variation in the timing of annual severe bleaching (ASB) conditions, a point at which reefs are certain to change and recovery will be limited. However, previous model-resolution projections (~1° × 1°) are too coarse to inform conservation planning. To meet the need for higher-resolution projections, we generated statistically downscaled projections (4-km resolution) for all coral reefs; these projections reveal high local-scale variation in ASB. Timing of ASB varies >10 years in 71 of the 87 countries and territories with >500 km2 of reef area. Emissions scenario RCP4.5 represents lower emissions mid-century than will eventuate if pledges made following the 2015 Paris Climate Change Conference (COP21) become reality. These pledges do little to provide reefs with more time to adapt and acclimate prior to severe bleaching conditions occurring annually. RCP4.5 adds 11 years to the global average ASB timing when compared to RCP8.5; however, >75% of reefs still experience ASB before 2070 under RCP4.5. Coral reef futures clearly vary greatly among and within countries, indicating the projections warrant consideration in most reef areas during conservation and management planning.

  29. Anthony, K.R.N., P.A. Marshall, A. Abdulla, R. Beeden, C. Bergh, R. Black, C.M. Eakin, E.T. Game, M. Gooch, N.A.J. Graham, A. Green, S.F. Heron, R. van Hooidonk, C. Knowland, S. Mangubhai, N. Marshall, J.A. Maynard, P. McGinnity, E. McLeod, P.J. Mumby, M. Nystrom, D. Obura, J. Oliver, H.P. Possingham, R.L. Pressey, G.P. Rowlands, J. Tamelander, D. Wachenfeld, and S. Wear. Operationalizing resilience for adaptive coral reef management under global environmental change. Global Change Biology, 21(1):48-61, https://doi.org/10.1111/gcb.12700 2015

    Abstract:

    Cumulative pressures from global climate and ocean change combined with multiple regional and local-scale stressors pose fundamental challenges to coral reef managers worldwide. Understanding how cumulative stressors affect coral reef vulnerability is critical for successful reef conservation now and in the future. In this review, we present the case that strategically managing for increased ecological resilience (capacity for stress resistance and recovery) can reduce coral reef vulnerability (risk of net decline) up to a point. Specifically, we propose an operational framework for identifying effective management levers to enhance resilience and support management decisions that reduce reef vulnerability. Building on a system understanding of biological and ecological processes that drive resilience of coral reefs in different environmental and socio-economic settings, we present an Adaptive Resilience-Based management (ARBM) framework and suggest a set of guidelines for how and where resilience can be enhanced via management interventions. We argue that press-type stressors (pollution, sedimentation, overfishing, ocean warming and acidification) are key threats to coral reef resilience by affecting processes underpinning resistance and recovery, while pulse-type (acute) stressors (e.g., storms, bleaching events, crown-of-thorns starfish outbreaks) increase the demand for resilience. We apply the framework to a set of example problems for Caribbean and Indo-Pacific reefs. A combined strategy of active risk reduction and resilience support is needed, informed by key management objectives, knowledge of reef ecosystem processes and consideration of environmental and social drivers. As climate change and ocean acidification erode the resilience and increase the vulnerability of coral reefs globally, successful adaptive management of coral reefs will become increasingly difficult. Given limited resources, on-the-ground solutions are likely to focus increasingly on actions that support resilience at finer spatial scales, and that are tightly linked to ecosystem goods and services.

  30. Ekstrom, J.A., L. Suatoni, S.R. Cooley, L.H. Pendleton, G.G. Waldbusser, J.E. Cinner, J. Ritter, C. Langdon, R. van Hooidonk, D. Gledhill, K. Wellman, M.W. Beck, L.M. Brander, D. Rittschof, C. Doherty, P.E.T. Edwards, and R. Portela. Vulnerability and adaptation of US shellfisheries to ocean acidification. Nature Climate Change, 5(3):207-214, https://doi.org/10.1038/nclimate2508 2015

    Abstract:

    Ocean acidification is a global, long-term problem whose ultimate solution requires carbon dioxide reduction at a scope and scale that will take decades to accomplish successfully. Until that is achieved, feasible and locally relevant adaptation and mitigation measures are needed. To help to prioritize societal responses to ocean acidification, we present a spatially explicit, multidisciplinary vulnerability analysis of coastal human communities in the United States. We focus our analysis on shelled mollusc harvests, which are likely to be harmed by ocean acidification. Our results highlight US regions most vulnerable to ocean acidification (and why), important knowledge and information gaps, and opportunities to adapt through local actions. The research illustrates the benefits of integrating natural and social sciences to identify actions and other opportunities while policy, stakeholders and scientists are still in relatively early stages of developing research plans and responses to ocean acidification.

  31. Maynard, J., R.J. van Hooidonk, C.M. Eakin, M. Puotinen, M. Garren, G. Williams, S.F. Heron, J. Lamb, E. Weil, B. Willis, and C.D. Harvell. Projections of climate conditions that increase coral disease susceptibility and pathogen abundance and virulence. Nature Climate Change, 5(7):688-694, https://doi.org/10.1038/nclimate2625 2015

    Abstract:

    Rising sea temperatures are likely to increase the frequency of disease outbreaks affecting reef-building corals through impacts on coral hosts and pathogens. We present and compare climate model projections of temperature conditions that will increase coral susceptibility to disease, pathogen abundance and pathogen virulence. Both moderate (RCP 4.5) and fossil fuel aggressive (RCP 8.5) emissions scenarios are examined. We also compare projections for the onset of disease-conducive conditions and severe annual coral bleaching, and produce a disease risk summary that combines climate stress with stress caused by local human activities. There is great spatial variation in the projections, both among and within the major ocean basins, in conditions favouring disease development. Our results indicate that disease is as likely to cause coral mortality as bleaching in the coming decades. These projections identify priority locations to reduce stress caused by local human activities and test management interventions to reduce disease impacts.

  32. Maynard, J., S. McKagan, L. Raymundo, S. Johnson, G. Ahmadia, L. Johnston, P. Houk, G. Williams, M. Kendall, S. Heron, R. van Hooidonk, and E. McLeod. Assessing relative resilience potential of coral reefs to inform management in the Commonwealth of the Northern Mariana Islands. NOAA Coral Reef Conservation Program, NOAA Technical Memorandum CRCP-22, 153 pp., 2015

    Abstract: No abstract.

  33. Maynard, J.A., S. McKagan, L. Raymundo, S. Johnson, G.N. Ahmadia, L. Johnston, P. Houk, G.J. Williams, M. Kendall, S.F. Heron, R. van Hooidonk, E. Mcleod, D. Tracey, and S. Planes. Assessing relative resilience potential of coral reefs to inform management. Biological Conservation, 192:109-119, https://doi.org/10.1016/j.biocon.2015.09.001 2015

    Abstract: Ecological resilience assessments are an important part of resilience-based management (RBM) and can help prioritize and target management actions. Use of such assessments has been limited due to a lack of clear guidance on the assessment process. This study builds on the latest scientific advances in RBM to provide that guidance from a resilience assessment undertaken in the Commonwealth of the Northern Mariana Islands (CNMI). We assessed spatial variation in ecological resilience potential at 78 forereef sites near the populated islands of the CNMI: Saipan, Tinian/Aguijan, and Rota. The assessments are based on measuring indicators of resilience processes and are combined with information on anthropogenic stress and larval connectivity. We find great spatial variation in relative resilience potential with many high resilience sites near Saipan (5 of 7) and low resilience sites near Rota (7 of 9). Criteria were developed to identify priority sites for six types of management actions (e.g., conservation, land-based sources of pollution reduction, and fishery management and enforcement) and 51 of the 78 sites met at least one of the sets of criteria. The connectivity simulations developed indicate that Tinian and Aguijan are each roughly 10× the larvae source that Rota is and twice as frequent a destination. These results may explain the lower relative resilience potential of Rota reefs and indicates that actions in Saipan and Tinian/Aguijan will be important to maintaining a supply of larvae. The process we describe for undertaking resilience assessments can be tailored for use in coral reef areas globally and applied to other ecosystems.

  34. van Hooidonk, R., J.A. Maynard, Y. Liu, and S.-K. Lee. Downscaled projections of Caribbean coral bleaching that can inform conservation planning. Global Change Biology, 21(9):3389-3401, https://doi.org/10.1111/gcb.12901 2015

    Abstract:

    Projections of climate change impacts on coral reefs produced at the coarse resolution (~1°) of Global Climate Models (GCMs) have informed debate but have not helped target local management actions. Here, projections of the onset of annual coral bleaching conditions in the Caribbean under Representative Concentration Pathway (RCP) 8.5 are produced using an ensemble of 33 Coupled Model Intercomparison Project phase-5 models and via dynamical and statistical downscaling. A high-resolution (~11 km) regional ocean model (MOM4.1) is used for the dynamical downscaling. For statistical downscaling, sea surface temperature (SST) means and annual cycles in all the GCMs are replaced with observed data from the ~4-km NOAA Pathfinder SST dataset. Spatial patterns in all three projections are broadly similar; the average year for the onset of annual severe bleaching is 2040–2043 for all projections. However, downscaled projections show many locations where the onset of annual severe bleaching (ASB) varies 10 or more years within a single GCM grid cell. Managers in locations where this applies (e.g., Florida, Turks and Caicos, Puerto Rico, and the Dominican Republic, among others) can identify locations that represent relative albeit temporary refugia. Both downscaled projections are different for the Bahamas compared to the GCM projections. The dynamically downscaled projections suggest an earlier onset of ASB linked to projected changes in regional currents, a feature not resolved in GCMs. This result demonstrates the value of dynamical downscaling for this application and means statistically downscaled projections have to be interpreted with caution. However, aside from west of Andros Island, the projections for the two types of downscaling are mostly aligned; projected onset of ASB is within ±10 years for 72% of the reef locations.

  35. Yates, K.K., C. Turley, B.M. Hopkinson, A.E. Todgham, J.N. Cross, H. Greening, P. Williamson, R. van Hooidonk, D.D. Deheyn, and Z. Johnson. Transdisciplinary science: A path to understanding the interactions among ocean acidification, ecosystems, and society. Oceanography, 28(2):212-225, https://doi.org/10.5670/oceanog.2015.43 2015

    Abstract:

    The global nature of ocean acidification (OA) transcends habitats, ecosystems, regions, and science disciplines. The scientific community recognizes that the biggest challenge in improving understanding of how changing OA conditions affect ecosystems, and associated consequences for human society, requires integration of experimental, observational, and modeling approaches from many disciplines over a wide range of temporal and spatial scales. Such transdisciplinary science is the next step in providing relevant, meaningful results and optimal guidance to policymakers and coastal managers. We discuss the challenges associated with integrating ocean acidification science across funding agencies, institutions, disciplines, topical areas, and regions, and the value of unifying science objectives and activities to deliver insights into local, regional, and global scale impacts. We identify guiding principles and strategies for developing transdisciplinary research in the ocean acidification science community.

  36. Enochs, I.C., D.P. Manzello, R. Carlton, S. Schopmeyer, R. van Hooidonk, and D. Lirman. Effects of light and elevated pCO2 on the growth and photochemical efficiency of Acropora cervicornis. Coral Reefs, 33(2):477-485, https://doi.org/10.1007/s00338-014-1132-7 2014

    Abstract:

    The effects of light and elevated pCO2 on the growth and photochemical efficiency of the critically endangered staghorn coral, Acropora cervicornis, were examined experimentally. Corals were subjected to high and low treatments of CO2 and light in a fully crossed design and monitored using 3D scanning and buoyant weight methodologies. Calcification rates, linear extension, as well as colony surface area and volume of A. cervicornis were highly dependent on light intensity. At pCO2 levels projected to occur by the end of the century from ocean acidification (OA), A. cervicornis exhibited depressed calcification, but no change in linear extension. Photochemical efficiency (F v/F m) was higher at low light, but unaffected by CO2. Amelioration of OA-depressed calcification under high-light treatments was not observed, and we suggest that the high-light intensity necessary to reach saturation of photosynthesis and calcification in A. cervicornis may limit the effectiveness of this potentially protective mechanism in this species. High CO2 causes depressed skeletal density, but not linear extension, illustrating that the measurement of extension by itself is inadequate to detect CO2 impacts. The skeletal integrity of A. cervicornis will be impaired by OA, which may further reduce the resilience of the already diminished populations of this endangered species.

  37. van Hooidonk, R., J.A. Maynard, D. Manzello, and S. Planes. Opposite latitudinal gradients in projected ocean acidification and bleaching impacts on coral reefs. Global Change Biology, 20(1):103-112, https://doi.org/10.1111/gcb.12394 2014

    Abstract:

    Coral reefs and the services they provide are seriously threatened by ocean acidification and climate change impacts like coral bleaching. Here, we present updated global projections for these key threats to coral reefs based on ensembles of IPCC AR5 climate models using the new Representative Concentration Pathway (RCP) experiments. For all tropical reef locations, we project absolute and percentage changes in aragonite saturation state (Ωarag) for the period between 2006 and the onset of annual severe bleaching (thermal stress >8 degree heating weeks); a point at which it is difficult to believe reefs can persist as we know them. Severe annual bleaching is projected to start 10–15 years later at high-latitude reefs than for reefs in low latitudes under RCP8.5. In these 10–15 years, Ωarag keeps declining and thus any benefits for high-latitude reefs of later onset of annual bleaching may be negated by the effects of acidification. There are no long-term refugia from the effects of both acidification and bleaching. Of all reef locations, 90% are projected to experience severe bleaching annually by 2055. Furthermore, 5% declines in calcification are projected for all reef locations by 2034 under RCP8.5, assuming a 15% decline in calcification per unit of Ωarag. Drastic emissions cuts, such as those represented by RCP6.0, result in an average year for the onset of annual severe bleaching that is ~20 years later (2062 vs. 2044). However, global emissions are tracking above the current worst-case scenario devised by the scientific community, as has happened in previous generations of emission scenarios. The projections here for conditions on coral reefs are dire, but provide the most up-to-date assessment of what the changing climate and ocean acidification mean for the persistence of coral reefs.

  38. van Hooidonk, R., J.A. Maynard, and S. Planes. Temporary refugia for coral reefs in a warming world. Nature Climate Change, 3(5):508-511, https://doi.org/10.1038/nclimate1829 2013

    Abstract:

    Climate-change impacts on coral reefs are expected to include temperature-induced spatially extensive bleaching events. Bleaching causes mortality when temperature stress persists but exposure to bleaching conditions is not expected to be spatially uniform at the regional or global scale. Here we show the first maps of global projections of bleaching conditions based on ensembles of IPCC AR5 models forced with the new Representative Concentration Pathways (RCPs). For the three RCPs with larger CO2 emissions (RCP 4.5, 6.0, and 8.5), the onset of annual bleaching conditions is associated with ~510 ppm CO2 equivalent; the median year of all locations is 2040 for the fossil-fuel aggressive RCP 8.5. Spatial patterns in the onset of annual bleaching conditions are similar for each of the RCPs. For RCP 8.5, 26% of reef cells are projected to experience annual bleaching conditions more than 5 years later than the median. Some of these temporary refugia include the western Indian Ocean, Thailand, the southern Great Barrier Reef and central French Polynesia. A reduction in the growth of greenhouse-gas emissions corresponding to the difference between RCP 8.5 and 6.0 delays annual bleaching in ~23% of reef cells more than two decades, which might conceivably increase the potential for these reefs to cope with these changes.

  39. van Hooidonk, R., and M. Huber. Effects of modeled tropical sea surface temperature variability on coral reef bleaching predictions. Coral Reefs, 31(1):121-131, https://doi.org/10.1007/s00338-011-0825-4 2012

    Abstract:

    Future widespread coral bleaching and subsequent mortality has been projected using sea surface temperature (SST) data derived from global, coupled ocean-atmosphere general circulation models (GCMs). While these models possess fidelity in reproducing many aspects of climate, they vary in their ability to correctly capture such parameters as the tropical ocean seasonal cycle and El Niño Southern Oscillation (ENSO) variability. Such weaknesses most likely reduce the accuracy of predicting coral bleaching, but little attention has been paid to the important issue of understanding potential errors and biases, the interaction of these biases with trends, and their propagation in predictions. To analyze the relative importance of various types of model errors and biases in predicting coral bleaching, various intra- and inter-annual frequency bands of observed SSTs were replaced with those frequencies from 24 GCMs 20th century simulations included in the Intergovernmental Panel on Climate Change (IPCC) 4th assessment report. Subsequent thermal stress was calculated and predictions of bleaching were made. These predictions were compared with observations of coral bleaching in the period 1982-2007 to calculate accuracy using an objective measure of forecast quality, the Peirce skill score (PSS). Major findings are that: (1) predictions are most sensitive to the seasonal cycle and inter-annual variability in the ENSO 24-60 months frequency band and (2) because models tend to understate the seasonal cycle at reef locations, they systematically underestimate future bleaching. The methodology we describe can be used to improve the accuracy of bleaching predictions by characterizing the errors and uncertainties involved in the predictions.

  40. van Hooidonk, R.J., D.P. Manzello, J. Moye, M.E. Brandt, J.C. Hendee, C. McCoy, and C. Manfrino. Coral bleaching at Little Cayman, Cayman Islands, 2009. Estuarine, Coastal and Shelf Science, 106:80-84, https://doi.org/10.1016/j.ecss.2012.04.021 2012

    Abstract:

    The global rise in sea temperature through anthropogenic climate change is affecting coral reef ecosystems through a phenomenon known as coral bleaching; that is, the whitening of corals due to the loss of the symbiotic zooxanthellae which impart corals with their characteristic vivid coloration. We describe aspects of the most prevalent episode of coral bleaching ever recorded at Little Cayman, Cayman Islands, during the fall of 2009. The most susceptible corals were found to be, in order, Siderastrea siderea, Montastraea annularis, and Montastraea faveolata, while Diplora strigosa and Agaricia spp. were less so, yet still showed considerable bleaching prevalence and severity. Those found to be least susceptible were Porites porites, Porites astreoides, and Montastraea cavernosa. These observations and other reported observations of coral bleaching, together with 29 years (1982-2010) of satellite-derived sea surface temperatures, were used to optimize bleaching predictions at this location. To do this a Degree Heating Weeks (DHW) and Peirce Skill Score (PSS) analysis were employed to calculate a local bleaching threshold above which bleaching was expected to occur. A threshold of 4.2 DHW had the highest skill, with a PSS of 0.70. The method outlined here could be applied to other regions to find the optimal bleaching threshold and improve bleaching predictions.