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Increasing hypoxia on global coral reefs under ocean warming

Abstract

Ocean deoxygenation is predicted to threaten marine ecosystems globally. However, current and future oxygen concentrations and the occurrence of hypoxic events on coral reefs remain underexplored. Here, using autonomous sensor data to explore oxygen variability and hypoxia exposure at 32 representative reef sites, we reveal that hypoxia is already pervasive on many reefs. Eighty-four percent of reefs experienced weak to moderate (≤153 µmol O2 kg−1 to ≤92 µmol O2 kg−1) hypoxia and 13% experienced severe (≤61 µmol O2 kg−1) hypoxia. Under different climate change scenarios based on four Shared Socioeconomic Pathways (SSPs), we show that projected ocean warming and deoxygenation will increase the duration, intensity and severity of hypoxia, with more than 94% and 31% of reefs experiencing weak to moderate and severe hypoxia, respectively, by 2100 under SSP5-8.5. This projected oxygen loss could have negative consequences for coral reef taxa due to the key role of oxygen in organism functioning and fitness.

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Fig. 1: Oxygen sensor deployment sites and locations, hourly oxygen climatologies and oxygen distributions on global coral reefs.
Fig. 2: Shifts in DO concentration, hypoxic event duration and occurrence of hypoxia exposure under warming on global coral reef sites.
Fig. 3: Timing of present-day hypoxic observations across global coral reef sites.

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Data availability

All data included in this study (for all figures and statistics56) are freely available on Dryad (https://doi.org/10.5061/dryad.41ns1rnj7). Data may be used if cited appropriately.

Code availability

All code files written and used for analyses in this study57 are freely available on GitHub (https://github.com/apezner/GlobalReefOxygen). Code may be used if cited appropriately.

References

  1. Stramma, L., Johnson, G. C., Sprintall, J. & Mohrholz, V. Expanding oxygen-minimum zones in the tropical oceans. Science 320, 655–658 (2008).

    Article  CAS  Google Scholar 

  2. Keeling, R. F., Körtzinger, A. & Gruber, N. Ocean deoxygenation in a warming world. Ann. Rev. Mar. Sci. 2, 199–229 (2010).

    Article  Google Scholar 

  3. Breitburg, D. et al. Declining oxygen in the global ocean and coastal waters. Science 359, eaam7240 (2018).

    Article  Google Scholar 

  4. Bopp, L. et al. Multiple stressors of ocean ecosystems in the 21st century: projections with CMIP5 models. Biogeosciences 10, 6225–6245 (2013).

    Article  Google Scholar 

  5. Kwiatkowski, L. et al. Twenty-first century ocean warming, acidification, deoxygenation, and upper-ocean nutrient and primary production decline from CMIP6 model projections. Biogeosciences 17, 3439–3470 (2020).

    Article  CAS  Google Scholar 

  6. Diaz, R. J. & Rosenberg, R. Marine benthic hypoxia: a review of its ecological effects and the behavioural responses of benthic macrofauna. Oceanogr. Mar. Biol. 33, 245–303 (1995).

    Google Scholar 

  7. Altieri, A. H. et al. Tropical dead zones and mass mortalities on coral reefs. Proc. Natl Acad. Sci. USA 114, 3660–3665 (2017).

    Article  CAS  Google Scholar 

  8. Nelson, H. R. & Altieri, A. H. Oxygen: the universal currency on coral reefs. Coral Reefs 38, 177–198 (2019).

    Article  Google Scholar 

  9. Hughes, D. J. et al. Coral reef survival under accelerating ocean deoxygenation. Nat. Clim. Change 10, 296–307 (2020).

    Article  CAS  Google Scholar 

  10. Kealoha, A. K. et al. Localized hypoxia may have caused coral reef mortality at the Flower Garden Banks. Coral Reefs 39, 119–132 (2020).

    Article  Google Scholar 

  11. Frölicher, T. L., Fischer, E. M. & Gruber, N. Marine heatwaves under global warming. Nature 560, 360–364 (2018).

    Article  Google Scholar 

  12. Vaquer-Sunyer, R., Duarte, C. M., Jordà, G. & Ruiz-Halpern, S. Temperature dependence of oxygen dynamics and community metabolism in a shallow Mediterranean macroalgal meadow (Caulerpa prolifera). Estuaries Coast. 35, 1182–1192 (2012).

    Article  CAS  Google Scholar 

  13. Sutherland, W. J. et al. A 2021 horizon scan of emerging global biological conservation issues. Trends Ecol. Evol. 36, 87–97 (2021).

    Article  Google Scholar 

  14. Cyronak, T. et al. Diel temperature and pH variability scale with depth across diverse coral reef habitats. Limnol. Oceanogr. Lett. 5, 193–203 (2020).

    Article  Google Scholar 

  15. Gray, J. S., Wu, R. S. S. & Or, Y. Y. Effects of hypoxia and organic enrichment on the coastal marine environment. Mar. Ecol. Prog. Ser. 238, 249–279 (2002).

    Article  Google Scholar 

  16. Vaquer-Sunyer, R. & Duarte, C. M. Thresholds of hypoxia for marine biodiversity. Proc. Natl Acad. Sci. USA 105, 15452–15457 (2008).

    Article  CAS  Google Scholar 

  17. Vaquer-Sunyer, R. & Duarte, C. M. Temperature effects on oxygen thresholds for hypoxia in marine benthic organisms. Glob. Change Biol. 17, 1788–1797 (2011).

    Article  Google Scholar 

  18. Haas, A. F., Smith, J. E., Thompson, M. & Deheyn, D. D. Effects of reduced dissolved oxygen concentrations on physiology and fluorescence of hermatypic corals and benthic algae. PeerJ 2, e235 (2014).

    Article  Google Scholar 

  19. Johnson, M. D., Swaminathan, S. D., Nixon, E. N., Paul, V. J. & Altieri, A. H. Differential susceptibility of reef-building corals to deoxygenation reveals remarkable hypoxia tolerance. Sci. Rep. 11, 23168 (2021).

    Article  CAS  Google Scholar 

  20. Gravinese, P. M., Douwes, A., Eaton, K. R. & Muller, E. M. Ephemeral hypoxia reduces oxygen consumption in the Caribbean coral Orbicella faveolata. Coral Reefs 41, 13–18 (2021).

    Article  Google Scholar 

  21. Nilsson, G. E., Östlund-Nilsson, S. & Munday, P. L. Effects of elevated temperature on coral reef fishes: loss of hypoxia tolerance and inability to acclimate. Comp. Biochem. Physiol. 156, 389–393 (2010).

    Article  Google Scholar 

  22. DeCarlo, T. M. et al. Mass coral mortality under local amplification of 2 °C ocean warming. Sci. Rep. 7, 44586 (2017).

  23. Hauri, C., Gruber, N., McDonnell, A. M. P. & Vogt, M. The intensity, duration, and severity of low aragonite saturation state events on the California continental shelf. Geophys. Res. Lett. 40, 3424–3428 (2013).

    Article  Google Scholar 

  24. Guzmán, H. M., Cortés, J., Glynn, P. W. & Richmond, R. H. Coral mortality associated with dinoflagellate blooms in the Eastern Pacific (Costa Rica and Panama). Mar. Ecol. Prog. Ser. 60, 299–303 (1990).

    Article  Google Scholar 

  25. Raj, K. D. et al. Low oxygen levels caused by Noctiluca scintillans bloom kills corals in Gulf of Mannar, India. Sci. Rep. 10, 22133 (2020).

    Article  CAS  Google Scholar 

  26. Johnson, M. D. et al. Rapid ecosystem-scale consequences of acute deoxygenation on a Caribbean coral reef. Nat. Commun. 12, 4522 (2021).

    Article  CAS  Google Scholar 

  27. Andréfouët, S., Dutheil, C., Menkes, C. E., Bador, M. & Lengaigne, M. Mass mortality events in atoll lagoons: environmental control and increased future vulnerability. Glob. Change Biol. 21, 195–205 (2015).

    Article  Google Scholar 

  28. Altieri, A. H. & Gedan, K. B. Climate change and dead zones. Glob. Change Biol. 21, 1395–1406 (2015).

    Article  Google Scholar 

  29. Murphy, J. W. A. & Richmond, R. H. Changes to coral health and metabolic activity under oxygen deprivation. PeerJ 4, e1956 (2016).

    Article  Google Scholar 

  30. Alderdice, R. et al. Divergent expression of hypoxia response systems under deoxygenation in reef‐forming corals aligns with bleaching susceptibility. Glob. Change Biol. 27, 312–326 (2021).

    Article  CAS  Google Scholar 

  31. Al-Horani, F. A., Tambutté, É. & Allemand, D. Dark calcification and the daily rhythm of calcification in the scleractinian coral, Galaxea fascicularis. Coral Reefs 26, 531–538 (2007).

    Article  Google Scholar 

  32. Wijgerde, T., Jurriaans, S., Hoofd, M., Verreth, J. A. J. & Osinga, R. Oxygen and heterotrophy affect calcification of the scleractinian coral Galaxea fascicularis. PLoS ONE 7, e52702 (2012).

    Article  CAS  Google Scholar 

  33. Wijgerde, T., Silva, C. I. F., Scherders, V., van Bleijswijk, J. & Osinga, R. Coral calcification under daily oxygen saturation and pH dynamics reveals the important role of oxygen. Biol. Open 3, 489–493 (2014).

    Article  Google Scholar 

  34. Deleja, M. et al. Effects of hypoxia on coral photobiology and oxidative stress. Biology 11, 1068 (2022).

  35. Alderdice, R. et al. Hypoxia as a physiological cue and pathological stress for coral larvae. Mol. Ecol. 31, 571–587 (2022).

    Article  CAS  Google Scholar 

  36. Alderdice, R. et al. Disparate inventories of hypoxia gene sets across corals align with inferred environmental resilience. Front. Mar. Sci. 9, 834332 (2022).

  37. Jorissen, H. & Nugues, M. M. Coral larvae avoid substratum exploration and settlement in low-oxygen environments. Coral Reefs 9, 31–39 (2021).

    Article  Google Scholar 

  38. Villanueva, R. D., Yap, H. T. & Montaño, M. N. E. Survivorship of coral juveniles in a fish farm environment. Mar. Pollut. Bull. 10, 580–589 (2005).

    Article  Google Scholar 

  39. Pörtner, H.-O., Bock, C. & Mark, F. C. Oxygen- and capacity-limited thermal tolerance: Bridging ecology and physiology. J. Exp. Biol. 220, 2685–2696 (2017).

    Article  Google Scholar 

  40. Deutsch, C., Ferrel, A., Seibel, B., Pörtner, H.-O. & Huey, R. B. Climate change tightens a metabolic constraint on marine habitats. Science 348, 1132–1135 (2015).

    Article  CAS  Google Scholar 

  41. Alderdice, R. et al. Deoxygenation lowers the thermal threshold of coral bleaching. Sci. Rep. 12, 18273 (2022).

    Article  CAS  Google Scholar 

  42. Steckbauer, A., Klein, S. G. & Duarte, C. M. Additive impacts of deoxygenation and acidification threaten marine biota. Glob. Change Biol. 26, 5602–5612 (2020).

    Article  Google Scholar 

  43. Cai, W. J. et al. Acidification of subsurface coastal waters enhanced by eutrophication. Nat. Geosci. 4, 766–770 (2011).

    Article  CAS  Google Scholar 

  44. D’Angelo, C. & Wiedenmann, J. Impacts of nutrient enrichment on coral reefs: new perspectives and implications for coastal management and reef survival. Curr. Opin. Environ. Sustain. 7, 82–93 (2014).

    Article  Google Scholar 

  45. Grégoire, M. et al. A global ocean oxygen database and atlas for assessing and predicting deoxygenation and ocean health in the open and coastal ocean. Front. Mar. Sci. 8, 724913 (2021).

  46. Yates, K. K., Moore, C. S. & Smiley, N. A. Time Series of Autonomous Carbonate System Parameter Measurements from Crocker Reef, Florida, USA (US Geological Survey, 2019); https://doi.org/10.5066/P90NCI8T

  47. Kekuewa, S. A. H. et al. Temporal and spatial variabilities of chemical and physical parameters on the Heron Island coral reef platform. Aquat. Geochem. 27, 241–268 (2021).

    Article  CAS  Google Scholar 

  48. Pedersen, K. A. Spatiotemporal Variability in Seawater Carbonate Chemistry at Two Contrasting Reef Locations in Bocas del Toro, Panama. MSc thesis, Univ. California (2019).

  49. Page, H. N. et al. Spatiotemporal variability in seawater carbon chemistry for a coral reef flat in Kāne’ohe Bay, Hawai’i. Limnol. Oceanogr. 64, 913–934 (2018).

    Article  Google Scholar 

  50. Pezner, A. K. et al. Lateral, vertical, and temporal variability of seawater carbonate chemistry at Hog Reef, Bermuda. Front. Mar. Sci. 8, 1–18 (2021).

    Article  Google Scholar 

  51. Ecosystem Sciences Division National Coral Reef Monitoring Program: Diel Seawater Carbonate Chemistry Observations from a Suite of Instrumentation Deployed at Coral Reef Sites at Tutuila Island, American Samoa from June 23 to July 17, 2018 NCEI Accession 0240606 (Pacific Islands Fisheries Science Center, 2021).

  52. Ecosystem Sciences Division National Coral Reef Monitoring Program: Diel Seawater Carbonate Chemistry Observations from a Suite of Instrumentation Deployed at Coral Reef Sites at Baker Island, Jarvis Island, and Palmyra Atoll in the Pacific Remote Islands Marine National Monument Between 2018-06-12 and 2018-08-07 NCEI Accession 0240686 (Pacific Islands Fisheries Science Center, 2021).

  53. Rintoul, M. S. et al. The effects of light intensity and flow speed on biogeochemical variability within a fringing coral reef in Onna‐son, Okinawa, Japan. J. Geophys. Res. Oceans 127, e2021JC018369 (2022).

    Article  CAS  Google Scholar 

  54. Kelley, D. & Richards, C. gsw: Gibbs sea water functions. R package version 1.0-5 https://CRAN.R-project.org/package=gsw (2017).

  55. RStudio Team RStudio: Integrated Development for R (RStudio, 2020).

  56. Pezner, A. K. et al. Data for: Increasing hypoxia on global coral reefs under ocean warming. Dryad https://doi.org/10.5061/dryad.41ns1rnj7 (2023).

  57. Pezner, A. K. et al. Global reef oxygen. GitHub https://github.com/apezner/GlobalReefOxygen (2023).

  58. Kennedy, E. V. et al. Reef cover, a coral reef classification for global habitat mapping from remote sensing. Sci. Data 8, 196 (2021).

    Article  Google Scholar 

  59. Dowle, M. & Srinivasan, A. data.table: extension of ‘data.frame’. R package version 1.13.6 https://CRAN.R-project.org/package=data.table (2020).

  60. Rosenberg, R. in Fjord Oceanography: Effects of Oxygen Deficiency on Benthic Macrofauna in Fjord oceanography, H. J. Freeland, D. M. Farmer, and C. D. Levings (eds), 499–514 (Plenum Press, 1980).

  61. Hofmann, A. F., Peltzer, E. T., Walz, P. M. & Brewer, P. G. Hypoxia by degrees: establishing definitions for a changing ocean. Deep Sea Res. I 58, 1212–1226 (2011).

    Article  CAS  Google Scholar 

  62. Klein, S. G., Steckbauer, A. & Duarte, C. M. Defining CO2 and O2 syndromes of marine biomes in the Anthropocene. Glob. Change Biol. 26, 355–363 (2020).

    Article  Google Scholar 

  63. Danabasoglu, G. NCAR CESM2-WACCM Model Output Prepared for CMIP6 CMIP (Earth System Grid Federation, 2019); https://doi.org/10.22033/ESGF/CMIP6.10028

  64. Danabasoglu, G. NCAR CESM2-WACCM Model Output Prepared for CMIP6 ScenarioMIP (Earth System Grid Federation, 2019); https://doi.org/10.22033/ESGF/CMIP6.10101

  65. Garcia, H. E. & Gordon, L. I. Oxygen solubility in seawater: better fitting equations. Limnol. Oceanogr. 37, 1307–1312 (1992).

    Article  CAS  Google Scholar 

  66. Hochachka, P. W. & Somero, G. N. Biochemical Adaptations (Oxford Univ. Press, 2002).

  67. Brown, J. H., Gillooly, J. F., Allen, A. P., Savage, V. M. & West, G. B. Toward a metabolic theory of ecology. Ecology 85, 1771–1789 (2004).

    Article  Google Scholar 

  68. Clausen, C. D. & Roth, A. A. Effect of temperature and temperature adaptation on calcification rate in the hermatypic coral Pocillopora damicornis. Mar. Biol. 33, 93–100 (1975).

    Article  Google Scholar 

  69. Howe, S. A. & Marshall, A. T. Thermal compensation of metabolism in the temperate coral, Plesiastrea versipora (Lamarck, 1816). J. Exp. Mar. Biol. Ecol. 259, 231–248 (2001).

    Article  Google Scholar 

  70. Edmunds, P., Gates, R. & Gleason, D. The biology of larvae from the reef coral Porites astreoides, and their response to temperature disturbances. Mar. Biol. 139, 981–989 (2001).

    Article  Google Scholar 

  71. Edmunds, P. J. Effect of elevated temperature on aerobic respiration of coral recruits. Mar. Biol. 146, 655–663 (2005).

    Article  Google Scholar 

  72. Edmunds, P. J. Differential effects of high temperature on the respiration of juvenile Caribbean corals. Bull. Mar. Sci. 83, 453–464 (2008).

    Google Scholar 

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Acknowledgments

We thank K. Inoha, R.-W. Syu and all field station administrators and field assistants who were essential in collecting these datasets. Any use of trade, firm or product names is for descriptive purposes only and does not imply endorsement by the US Government. Funding was provided by the National Science Foundation: OCE-1255042 (A.J.A.), OCE-1829778 (A.J.A.), OCE-1538495 (D.I.K. and M.T.), OCE-1459255 (M.D.D) and OPP-1951294 (M.D.D); Belmont Forum/NSF ICER 2029205 (A.J.A.); UCSD Marine Sciences grant no. A105437 (A.J.A.); the National Science Foundation Graduate Research Fellowship DGE-2038238 (A.K.P.); a Philanthropic Educational Organization International Scholar Award (A.K.P.); the NOAA Coral Reef Conservation Program and NOAA Ocean Acidification Program, through the NOAA National Coral Reef Monitoring Program (H.C.B.); the US Geological Survey Coastal and Marine Hazards and Resources Program-funded data collection at Crocker Reef, Florida, USA (K.K.Y.46); internal funding from the Okinawa Institute of Science and Technology (S.M.); and the Ministry of Science and Technology of Taiwan grant no. 107-2611-M-019-001-MY3 (W.-C.C.). Funding for the long-term monitoring programme on Palmyra Atoll was provided to Smith Lab (J.E.S.) from the Bohn Family Foundation and the Bill and Kathy Scripps Family Foundation.

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A.K.P., T.A.C. and A.J.A. conceptualized the paper and methodology, with contributions from M.S.R. to methodology. A.K.P. performed the formal analysis and visualization, under supervision of T.A.C. and A.J.A. A.K.P. and A.J.A. wrote the original draft of the paper. All authors (A.K.P., T.A.C., H.C.B., W.-C.C., H.-C.C., S.M.C., T.C., M.D.G, S.A.H.K., D.I.K., Y.-B.L., T.R.M., S.M., H.N.P., M.S.R., J.E.S., K.S., Y.T., M.T., Y.W., K.K.Y. and A.J.A.) contributed to investigation as well as review and editing of the paper.

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Correspondence to Ariel K. Pezner.

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Extended data

Extended Data Fig. 1 Dissolved oxygen and temperature time series for global coral reef sites.

Dissolved oxygen (µmol O2 kg−1; black, left y-axis) and temperature (°C; blue, right y-axis) as a function of time in order of sites with increasing deployment length, ranging from 3 to 309 days (Supplementary Table 1). For each location, different instrument deployment sites are represented by numbers (for example, Dongsha 1 and Dongsha 2), or a combination of letters and numbers where letters represent either different depths at the same site (for example, Bocas 1a and 1b) or different deployments at the same site over time (for example, Crocker 1a, 1b, and 1c) (see Supplementary Table 1 for specific site information).

Extended Data Fig. 2 Nonlinear regressions between dissolved oxygen metrics, depth, and flow speed categorized by reef type.

(a) Dissolved oxygen (DO) variability (mean daily range in DO; µmol O2 kg−1; ± 1 standard deviation (s.d.)) as a function of mean depth (m; ± 1 s.d.) and (b) mean flow speed (m s−1; ± 1 s.d.) at global coral reef sites categorized by reef type (colors; Supplementary Table 1). (c) Mean daily minimum DO (µmol O2 kg−1; ± 1 s.d.) as a function of mean depth (m; ± 1 s.d.) and (d) mean flow speed (m s−1; ± 1 s.d.). For DO metrics, error bars represent ± 1 s.d. (n varies by site, see Supplementary Table 2). Measurements of flow speed and depth were only made at a subset of locations (n varied by site, see Supplementary Table 3). Error bars also represent ± 1 s.d. for the sites where these data were recorded. For sites where no current meter was deployed, recorded deployment depth was used instead of a calculated mean depth (no error bars plotted). Regression lines were plotted using power model regression statistics reported in Supplementary Table 4. No regression line is plotted in B due to poor fit.

Extended Data Fig. 3 Sea surface temperature predictions for global coral reef locations.

Mean monthly Coupled Model Intercomparison Project 6 (CMIP6) ensemble member Community Earth System Model 2 Whole Atmosphere Community Climate Model (CESM2-WACCM)63,64 sea surface temperature (SST) projections at global coral reef sites for the Shared Socioeconomic Pathways (SSPs) SSP1-2.6, SSP2-4.5, SSP3-7.0, and SSP5-8.5 scenarios (blue to red) between 2015 and 2100.

Extended Data Fig. 4 Conceptual diagram of calculation approach used to estimate changes in coral reef dissolved oxygen under warming (Equations 613).

(a) Present-day dissolved oxygen (DO; µmol O2 kg−1; solid grey line), mean DO value across time series (purple dashed line; assumed to be close to equilibrium), approximation of drawdown of DO by respiration at night (DOoffset; yellow arrow) expressed as the difference between mean DO and mean daily minimum (DOmin; orange), and the projected increase in respiration under 3 °C warming using a Q10 relationship (∆DOQ10; pink arrow). (b) Present-day DO (solid grey line), present-day DO solubility (dashed dark blue line; DOsol present), DO solubility under 3 °C warming (dashed light blue line), and the calculated decrease in solubility under 3 °C warming (∆DOsol; green arrow). (c) Present-day DO (solid grey line) and new calculated DO under 3 °C warming (black solid line) due to increased respiration and decreased solubility (pink and green arrows, respectively).

Extended Data Fig. 5 Box model simulations and validation of calculation approach to estimate dissolved oxygen changes as a result of warming.

(a) Modeled variations in seawater dissolved oxygen (DO; µmol O2 kg−1) in a hypothetical coral reef system over 7 days under three temperature scenarios (25 °C, 28 °C, and 31 °C; purple, green, blue, respectively) and two residence times (1 hour and 5 hours; solid and dotted lines, respectively). The model is described in detail in the Supplementary Information Extended Methods. (b) Comparison between the box model-calculated changes in DO due to warming and the calculation approach employed for the global coral reef dataset (Extended Data Fig. 4; Equations 613) represented as the deviation of model DO estimates from calculation DO estimates (µmol O2 kg−1). Comparisons were made for two warming scenarios relative to the base scenario of 25 °C (+3 °C and +6 °C; blue and green, respectively) and two residence times (1 hour and 5 hours; solid and dotted, respectively) over 7 days.

Extended Data Fig. 6 Total number of hypoxic observations and events for global coral reef sites under different warming scenarios and hypoxia thresholds.

(a) Total number of observations and (b) total number of hypoxic events below different hypoxia thresholds: 153 µmol O2 kg−1, 122 µmol O2 kg−1, 92 µmol O2 kg−1, and 61 µmol O2 kg−1 (weak, mild, moderate, and severe; light blue to dark blue) for different warming scenarios including 4 Shared Socioeconomic Pathways (SSPs) and a heatwave event across global coral reef sites.

Extended Data Fig. 7 Changes in the duration, intensity, and severity of hypoxic events under warming for global coral reef sites.

Distributions of the (a) duration (hours), (b) intensity (µmol O2 kg−1), and (c) severity (µmol O2 kg−1 hr) of hypoxic events below different oxygen thresholds (≤153 µmol O2 kg−1, ≤122 µmol O2 kg−1, ≤92 µmol O2 kg−1, or ≤61 µmol O2 kg−1) under present-day conditions and 5 different warming projections (including 4 Shared Socioeconomic Pathways (SSPs); blue to red) across global coral reef sites.

Extended Data Fig. 8 Changes in the cumulative duration, intensity, and severity of hypoxic events under warming for global coral reef sites.

(a) Cumulative duration (hours), (b) cumulative intensity (µmol O2 kg−1), and (c) cumulative severity (µmol O2 kg−1 hr) of hypoxic events below different oxygen thresholds (≤153 µmol O2 kg−1, ≤122 µmol O2 kg−1, ≤92 µmol O2 kg−1, or ≤61 µmol O2 kg−1; shades of blue) for different warming scenarios including 4 Shared Socioeconomic Pathways (SSPs) and a heatwave event across global coral reef sites.

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Pezner, A.K., Courtney, T.A., Barkley, H.C. et al. Increasing hypoxia on global coral reefs under ocean warming. Nat. Clim. Chang. 13, 403–409 (2023). https://doi.org/10.1038/s41558-023-01619-2

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