Temperature-dependent hypoxia explains biogeography and severity of end-Permian marine mass extinction

Climate Change 2007: The Physical Science Basis.

Schiavon, S., & Zecchin, R. (2007) · eScholarship (California Digital Library) · Cited by 16,994

Climate change affects marine fishes through the oxygen limitation of thermal tolerance

Pörtner, H. O., & Knust, R. (2007) · Science · doi:10.1126/science.1135471 · Cited by 2,030

Multiple stressors of ocean ecosystems in the 21st century: projections with CMIP5 models

Bopp, L., Resplandy, L., Orr, J. C., Doney, S. C., Dunne, J. P. P., Gehlen, M., Halloran, P. R., Heinze, C., Ilyina, T., Séférian, R., et al. (2013) · Biogeosciences · doi:10.5194/bg-10-6225-2013 · Cited by 1,809

High-latitude controls of thermocline nutrients and low latitude biological productivity

Sarmiento, J. L., Gruber, N., Brzezinski, M. A., & Dunne, J. P. P. (2003) · Nature · doi:10.1038/nature02127 · Cited by 1,402

Oceanic Anoxia and the End Permian Mass Extinction

Wignall, P. B., & Twitchett, R. J. (1996) · Science · doi:10.1126/science.272.5265.1155 · Cited by 1,206

Lethally Hot Temperatures During the Early Triassic Greenhouse

Sun, Y.-D., Joachimski, M., Wignall, P., Yan, C.-B., Chen, Y.-L., Jiang, H.-S., Wang, L., & Lai, X. (2012) · Science · doi:10.1126/science.1224126 · Cited by 980

Permo-Triassic Boundary Superanoxia and Stratified Superocean: Records from Lost Deep Sea

Isozaki, Y. (1997) · Science · doi:10.1126/science.276.5310.235 · Cited by 842

Photic Zone Euxinia During the Permian-Triassic Superanoxic Event

Grice, K., Cao, C., Love, G. D., Böttcher, M. E., Twitchett, R. J., Grosjean, E., Summons, R. E., Turgeon, S. C., Dunning, W., & Jin, Y. (2005) · Science · doi:10.1126/science.1104323 · Cited by 819

Climate change tightens a metabolic constraint on marine habitats

Deutsch, C., Ferrel, A., Seibel, B., Pörtner, H.-O., & Huey, R. B. (2015) · Science · doi:10.1126/science.aaa1605 · Cited by 747

High-precision timeline for Earth’s most severe extinction

Burgess, S. D., Bowring, S. A., & Shen, S. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1317692111 · Cited by 734

Climate Endgame: Exploring catastrophic climate change scenarios

Kemp, L., Xu, C., Depledge, J., Ebi, K. L., Gibbins, G., Kohler, T. A., Rockström, J., Scheffer, M., Schellnhuber, H. J., Steffen, W., et al. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2108146119 · Cited by 918

Greater vulnerability to warming of marine versus terrestrial ectotherms

Pinsky, M. L., Eikeset, A. M., McCauley, D. J., Payne, J. L., & Sunday, J. M. (2019) · Nature · doi:10.1038/s41586-019-1132-4 · Cited by 780

A global analysis of coral bleaching over the past two decades

Sully, S., Burkepile, D. E., Donovan, M. K., Hodgson, G., & van Woesik, R. (2019) · Nature Communications · doi:10.1038/s41467-019-09238-2 · Cited by 681

Climate-Driven Shifts in Marine Species Ranges: Scaling from Organisms to Communities

Pinsky, M. L., Selden, R. L., & Kitchel, Z. J. (2019) · Annual Review of Marine Science · doi:10.1146/annurev-marine-010419-010916 · Cited by 689

Biogeochemical extremes and compound events in the ocean

Gruber, N., Boyd, P. W., Frölicher, T. L., & Vogt, M. (2021) · Nature · doi:10.1038/s41586-021-03981-7 · Cited by 385

Impacts of hypoxic events surpass those of future ocean warming and acidification

Sampaio, E., Santos, C., Rosa, I. C., Ferreira, V., Pörtner, H.-O., Duarte, C. M., Levin, L. A., & Rosa, R. (2021) · Nature Ecology & Evolution · doi:10.1038/s41559-020-01370-3 · Cited by 295

Metabolic trait diversity shapes marine biogeography

Deutsch, C. A., Penn, J. L., & Seibel, B. A. (2020) · Nature · doi:10.1038/s41586-020-2721-y · Cited by 264

Coral reef survival under accelerating ocean deoxygenation

Hughes, D. J., Alderdice, R., Cooney, C., Kühl, M., Pernice, M., Voolstra, C. R., & Suggett, D. J. (2020) · Nature Climate Change · doi:10.1038/s41558-020-0737-9 · Cited by 249

The appallingly bad neoclassical economics of climate change

Keen, S. (2020) · Globalizations · doi:10.1080/14747731.2020.1807856 · Cited by 229

Seawater Temperature and Dissolved Oxygen over the Past 500 Million Years

Song, H., Wignall, P. B., Song, H., Dai, X., & Chu, D. (2019) · Journal of Earth Science · doi:10.1007/s12583-018-1002-2 · Cited by 224

Environmental crises at the Permian–Triassic mass extinction

Corso, J. D., Song, H., Callegaro, S., Chu, D., Sun, Y., Hilton, J. M., Grasby, S. E., Joachimski, M. M., & Wignall, P. B. (2022) · Nature Reviews Earth & Environment · doi:10.1038/s43017-021-00259-4 · Cited by 218

Avoiding ocean mass extinction from climate warming

Penn, J. L., & Deutsch, C. A. (2022) · Science · doi:10.1126/science.abe9039 · Cited by 226

Coral‐bleaching responses to climate change across biological scales

van Woesik, R., Shlesinger, T., Grottoli, A. G., Toonen, R. J., Thurber, R. L. V., Warner, M. E., Hulver, A. M., Chapron, L., McLachlan, R. H., Albright, R., et al. (2022) · Global Change Biology · doi:10.1111/gcb.16192 · Cited by 209

The challenge of novel abiotic conditions for species undergoing climate‐induced range shifts

Spence, A. R., & Tingley, M. W. (2020) · Ecography · doi:10.1111/ecog.05170 · Cited by 163

Thresholds of temperature change for mass extinctions

Song, H., Kemp, D. B., Tian, L., Chu, D., Song, H., & Dai, X. (2021) · Nature Communications · doi:10.1038/s41467-021-25019-2 · Cited by 174

Point of Departure and Key Concepts

(IPCC), I. P. O. C. C. (2023) · Cambridge University Press eBooks · doi:10.1017/9781009325844.003 · Cited by 219

On the co‐evolution of surface oxygen levels and animals

Cole, D. B., Mills, D. B., Erwin, D. H., Sperling, E. A., Porter, S. M., Reinhard, C. T., & Planavsky, N. J. (2020) · Geobiology · doi:10.1111/gbi.12382 · Cited by 141

The ecological relevance of critical thermal maxima methodology for fishes

Desforges, J. E., Birnie‐Gauvin, K., Jutfelt, F., Gilmour, K. M., Martin, K., Eliason, E., Dressler, T., McKenzie, D. J., Bates, A., Lawrence, M., et al. (2023) · Journal of Fish Biology · doi:10.1111/jfb.15368 · Cited by 145

Scaling of thermal tolerance with body mass and genome size in ectotherms: a comparison between water- and air-breathers

Leiva, F. P., Calosi, P., & Verberk, W. C. E. P. (2019) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2019.0035 · Cited by 139

Six-fold increase of atmospheric pCO2 during the Permian–Triassic mass extinction

Wu, Y., Chu, D., Tong, J., Song, H., Corso, J. D., Wignall, P. B., Song, H., Du, Y., & Cui, Y. (2021) · Nature Communications · doi:10.1038/s41467-021-22298-7 · Cited by 120

Uranium isotopes in marine carbonates as a global ocean paleoredox proxy: A critical review

Zhang, F., Lenton, T. M., del Rey, Á., Romaniello, S. J., Chen, X., Planavsky, N. J., Clarkson, M. O., Dahl, T. W., Lau, K., Wang, W., et al. (2020) · Geochimica et Cosmochimica Acta · doi:10.1016/j.gca.2020.05.011 · Cited by 119

The late blooming amphipods: Global change promoted post-Jurassic ecological radiation despite Palaeozoic origin

Copilaş‐Ciocianu, D., Borko, Š., & Fišer, C. (2019) · Molecular Phylogenetics and Evolution · doi:10.1016/j.ympev.2019.106664 · Cited by 115

Siberian Trap volcanism, global warming and the Permian-Triassic mass extinction: New insights from Armenian Permian-Triassic sections

Joachimski, M. M., Alekseev, A. S., Grigoryan, A., & Gatovsky, Y. А. (2019) · Geological Society of America Bulletin · doi:10.1130/b35108.1 · Cited by 114

Climate-driven aerobic habitat loss in the California Current System

Howard, E. M., Penn, J. L., Frenzel, H., Seibel, B. A., Bianchi, D., Renault, L., Kessouri, F., Sutula, M. A., McWilliams, J. C., & Deutsch, C. A. (2020) · Science Advances · doi:10.1126/sciadv.aay3188 · Cited by 117

Circling the drain: the extinction crisis and the future of humanity

Dirzo, R., Ceballos, G., & Ehrlich, P. R. (2022) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2021.0378 · Cited by 123

Establishing the link between Permian volcanism and biodiversity changes: Insights from geochemical proxies

Chen, J., & Xu, Y. (2019) · Gondwana Research · doi:10.1016/j.gr.2019.04.008 · Cited by 103

Flat latitudinal diversity gradient caused by the Permian–Triassic mass extinction

Song, H., Huang, S., Jia, E., Dai, X., Wignall, P. B., & Dunhill, A. M. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1918953117 · Cited by 100

Thermal performance of the European flat oyster, Ostrea edulis (Linnaeus, 1758)—explaining ecological findings under climate change

Eymann, C., Götze, S., Bock, C., Guderley, H., Knoll, A. H., Lannig, G., Sokolova, I. M., Aberhan, M., & Pörtner, H. (2020) · Marine Biology · doi:10.1007/s00227-019-3620-3 · Cited by 97

Climate impacts on organisms, ecosystems and human societies: integrating OCLTT into a wider context

Pörtner, H. (2021) · Journal of Experimental Biology · doi:10.1242/jeb.238360 · Cited by 101

Climate-driven deoxygenation elevates fishing vulnerability for the ocean's widest ranging shark

Vedor, M., Queiroz, N. C., Mucientes, G., Couto, A., da Costa, I., dos Santos, A., Vandeperre, F., Fontes, J., Afonso, P., Rosa, R., et al. (2021) · eLife · doi:10.7554/elife.62508 · Cited by 108

Steroid receptors and vertebrate evolution

Baker, M. E. (2019) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2019.110526 · Cited by 94

The History of Ocean Oxygenation

Reinhard, C. T., & Planavsky, N. J. (2022) · Annual Review of Marine Science · doi:10.1146/annurev-marine-031721-104005 · Cited by 91

Global warming generates predictable extinctions of warm‐ and cold‐water marine benthic invertebrates via thermal habitat loss

Reddin, C. J., Aberhan, M., Raja, N. B., & Kocsis, Á. T. (2022) · Global Change Biology · doi:10.1111/gcb.16333 · Cited by 93

Two distinct episodes of marine anoxia during the Permian-Triassic crisis evidenced by uranium isotopes in marine dolostones

Zhang, F., Shen, S., Cui, Y., Lenton, T. M., Dahl, T. W., Zhang, H., Zheng, Q.-F., Wang, W., Krainer, K., & Anbar, A. D. (2020) · Geochimica et Cosmochimica Acta · doi:10.1016/j.gca.2020.01.032 · Cited by 87

Impact of warming on aquatic body sizes explained by metabolic scaling from microbes to macrofauna

Deutsch, C. A., Penn, J. L., Verberk, W. C. E. P., Inomura, K., Endress, M.-G., & Payne, J. L. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2201345119 · Cited by 81

Arctic Climate Change: Local Impacts, Global Consequences, and Policy Implications

Vincent, W. F. (2019) · Springer eBooks · doi:10.1007/978-3-030-20557-7_31 · Cited by 92

Continental configuration controls ocean oxygenation during the Phanerozoic

(2022) · doi:10.1038/s41586-022-05018-z · Cited by 82

What controls the duration and intensity of ocean anoxic events in the Paleozoic and the Mesozoic?

Reershemius, T., & Planavsky, N. J. (2021) · Earth-Science Reviews · doi:10.1016/j.earscirev.2021.103787 · Cited by 82

Sustained increases in atmospheric oxygen and marine productivity in the Neoproterozoic and Palaeozoic eras

Stockey, R. G., Cole, D. B., Farrell, U. C., Agić, H., Boag, T. H., Brocks, J. J., Canfield, D. E., Cheng, M., Crockford, P. W., Cui, H., et al. (2024) · Nature Geoscience · doi:10.1038/s41561-024-01479-1 · Cited by 78

Marine anoxia linked to abrupt global warming during Earth’s penultimate icehouse

Chen, J., Montañez, I. P., Zhang, S., Isson, T. T., Macarewich, S. I., Planavsky, N. J., Zhang, F., Rauzi, S., Daviau, K., Yao, L., et al. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2115231119 · Cited by 75

Improving the relevance of paleontology to climate change policy

Kiessling, W., Smith, J. A., & Raja, N. B. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2201926119 · Cited by 73

Climate, Oxygen, and the Future of Marine Biodiversity

Deutsch, C. A., Penn, J. L., & Lucey, N. (2023) · Annual Review of Marine Science · doi:10.1146/annurev-marine-040323-095231 · Cited by 78

Exploration of alkali cation variation on the synthesis of carbon nanotubes by electrolysis of CO2 in molten carbonates

Wang, X., Liu, X., Licht, G., Wang, B., & Licht, S. L. (2019) · Journal of CO2 Utilization · doi:10.1016/j.jcou.2019.07.007 · Cited by 71

Radiometric Constraints on the Timing, Tempo, and Effects of Large Igneous Province Emplacement

Kasbohm, J. J., Schoene, B., & Burgess, S. D. (2021) · Geophysical monograph · doi:10.1002/9781119507444.ch2 · Cited by 70

Marine clade sensitivities to climate change conform across timescales

Reddin, C. J., Nätscher, P., Kocsis, Á. T., Pörtner, H., & Kiessling, W. (2020) · Nature Climate Change · doi:10.1038/s41558-020-0690-7 · Cited by 69

Climate change is an important predictor of extinction risk on macroevolutionary timescales

Malanoski, C. M., Farnsworth, A., Lunt, D. J., Valdes, P. J., & Saupe, E. E. (2024) · Science · doi:10.1126/science.adj5763 · Cited by 71

Extinction intensity during Ordovician and Cenozoic glaciations explained by cooling and palaeogeography

Saupe, E. E., Qiao, H., Yannick Donnadieu, A., Farnsworth, A., Kennedy-Asser, A. T., Ladant, J., Lunt, D. J., Pohl, A., Valdes, P. J., & Finnegan, S. (2019) · Nature Geoscience · doi:10.1038/s41561-019-0504-6 · Cited by 68

Aerobic growth index (AGI): An index to understand the impacts of ocean warming and deoxygenation on global marine fisheries resources

Clarke, T. M., Wabnitz, C. C. C., Striegel, S., Frölicher, T. L., Reygondeau, G., & Cheung, W. W. L. (2021) · Progress In Oceanography · doi:10.1016/j.pocean.2021.102588 · Cited by 67

Ecological regime shift preserved in the Anthropocene stratigraphic record

Tomášových, A., Albano, P. G., Fuksi, T., Gallmetzer, I., Haselmair, A., Kowalewski, M., Nawrot, R., Nerlović, V., Scarponi, D., & Zuschin, M. (2020) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2020.0695 · Cited by 61

Decreasing Phanerozoic extinction intensity as a consequence of Earth surface oxygenation and metazoan ecophysiology

Stockey, R., Pohl, A., Ridgwell, A. J., Finnegan, S., & Sperling, E. A. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2101900118 · Cited by 62

Ammonium ocean following the end-Permian mass extinction

Sun, Y., Zulla, M., Joachimski, M. M., Bond, D. P. G., Wignall, P. B., Zhang, Z. T., & Zhang, M. (2019) · Earth and Planetary Science Letters · doi:10.1016/j.epsl.2019.04.036 · Cited by 59

Addressing priority questions of conservation science with palaeontological data

Kiessling, W., Raja, N. B., Roden, V. J., Turvey, S. T., & Saupe, E. E. (2019) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2019.0222 · Cited by 56

The latitudinal diversity gradient of tetrapods across the Permo-Triassic mass extinction and recovery interval

Allen, B. J., Wignall, P. B., Hill, D. J., Saupe, E. E., & Dunhill, A. M. (2020) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2020.1125 · Cited by 56

Renewable energy and biological conservation in a changing world

Jager, H. I., Efroymson, R. A., & McManamay, R. A. (2021) · Biological Conservation · doi:10.1016/j.biocon.2021.109354 · Cited by 62

Sedimentology of the continental end‐Permian extinction event in the Sydney Basin, eastern Australia

Fielding, C. R., Frank, T. D., Tevyaw, A. P., Savatic, K., Vajda, V., McLoughlin, S., Mays, C., Nicoll, R. S., Bocking, M., & Crowley, J. L. (2020) · Sedimentology · doi:10.1111/sed.12782 · Cited by 55

End-Permian marine extinction due to temperature-driven nutrient recycling and euxinia

Hülse, D., Lau, K., van de Velde, S., Arndt, S., MEYER, K. M., & Ridgwell, A. J. (2021) · Nature Geoscience · doi:10.1038/s41561-021-00829-7 · Cited by 57

Forty years later: The status of the “Big Five” mass extinctions

Marshall, C. R. (2023) · Cambridge Prisms Extinction · doi:10.1017/ext.2022.4 · Cited by 53

Transient Permian-Triassic euxinia in the southern Panthalassa deep ocean

Grasby, S. E., Bond, D. P. G., Wignall, P. B., Yin, R., Strachan, L. J., & Takahashi, S. (2021) · Geology · doi:10.1130/g48928.1 · Cited by 52

What global biogeochemical consequences will marine animal–sediment interactions have during climate change?

Bianchi, T. S., Aller, R. C., Atwood, T. B., Brown, C. J., Buatois, L. A., Levin, L. A., Levinton, J. S., Middelburg, J. J., Morrison, E. S., Regnier, P. A. G., et al. (2021) · Elementa Science of the Anthropocene · doi:10.1525/elementa.2020.00180 · Cited by 57

Single and combined effects of the “Deadly trio” hypoxia, hypercapnia and warming on the cellular metabolism of the great scallop Pecten maximus

Götze, S., Bock, C., Eymann, C., Lannig, G., Steffen, J. B. M., & Pörtner, H. (2020) · Comparative Biochemistry and Physiology Part B Biochemistry and Molecular Biology · doi:10.1016/j.cbpb.2020.110438 · Cited by 52

Integrated bio-chemostratigraphy of Lower and Middle Triassic marine successions at Spiti in the Indian Himalaya: Implications for the Early Triassic nutrient crisis

Sun, Y., Richoz, S., Krystyn, L., Grasby, S. E., Chen, Y., Banerjee, D. M., & Joachimski, M. M. (2020) · Global and Planetary Change · doi:10.1016/j.gloplacha.2020.103363 · Cited by 51

A multiscale view of the Phanerozoic fossil record reveals the three major biotic transitions

Rojas, A., Calatayud, J., Kowalewski, M., Neuman, M., & Rosvall, M. (2021) · Communications Biology · doi:10.1038/s42003-021-01805-y · Cited by 54

I/Ca in epifaunal benthic foraminifera: A semi-quantitative proxy for bottom water oxygen in a multi-proxy compilation for glacial ocean deoxygenation

Lu, W., Rickaby, R. E. M., Hoogakker, B. A. A., Rathburn, A. E., Burkett, A. M., Dickson, A. J., Méndez, G. M., Hillenbrand, C., Zhou, X., Thomas, E., et al. (2020) · Earth and Planetary Science Letters · doi:10.1016/j.epsl.2019.116055 · Cited by 55

Unifying climate change biology across realms and taxa

Pinsky, M. L., Comte, L., & Sax, D. F. (2022) · Trends in Ecology & Evolution · doi:10.1016/j.tree.2022.04.011 · Cited by 49

A framework for the integrated analysis of the magnitude, selectivity, and biotic effects of extinction and origination

Bush, A. M., Wang, S. C., Payne, J. L., & Heim, N. A. (2019) · Paleobiology · doi:10.1017/pab.2019.35 · Cited by 47

Oceanic redox evolution around the end-Permian mass extinction at Meishan, South China

Xiang, L., Zhang, H., Schoepfer, S. D., Cao, C., Zheng, Q.-F., Yuan, D., Cai, Y.-F., & Shen, S. (2020) · Palaeogeography Palaeoclimatology Palaeoecology · doi:10.1016/j.palaeo.2020.109626 · Cited by 47

Transient ocean oxygenation at end-Permian mass extinction onset shown by thallium isotopes

Newby, S. M., Owens, J. D., Schoepfer, S. D., & Algeo, T. J. (2021) · Nature Geoscience · doi:10.1038/s41561-021-00802-4 · Cited by 47

Impact of deoxygenation and warming on global marine species in the 21st century

Morée, A. L., Clarke, T. M., Cheung, W. W. L., & Frölicher, T. L. (2023) · Biogeosciences · doi:10.5194/bg-20-2425-2023 · Cited by 48

Powering Ocean Giants: The Energetics of Shark and Ray Megafauna

Lawson, C. L., Halsey, L. G., Hays, G. C., Dudgeon, C. L., Payne, N. L., Bennett, M. B., White, C. R., & Richardson, A. J. (2019) · Trends in Ecology & Evolution · doi:10.1016/j.tree.2019.07.001 · Cited by 50

The terrestrial end-Permian mass extinction in the paleotropics postdates the marine extinction

Wu, Q., Zhang, H., Ramezani, J., Zhang, F., Erwin, D. H., Feng, Z., Shao, L., Cai, Y.-F., Zhang, S., Xu, Y., et al. (2024) · Science Advances · doi:10.1126/sciadv.adi7284 · Cited by 43

High temperature methane emissions from Large Igneous Provinces as contributors to late Permian mass extinctions

Chen, C., Qin, S., Wang, Y., Holland, G., Wynn, P., Zhong, W., & Zhou, Z. (2022) · Nature Communications · doi:10.1038/s41467-022-34645-3 · Cited by 42

Earth History of Oxygen and the iprOxy

Lu, Z., Lu, W., Rickaby, R. E. M., & Thomas, E. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108688604 · Cited by 38

Dying in the Sun: Direct evidence for elevated UV-B radiation at the end-Permian mass extinction

Liu, F., Peng, H., Marshall, J. E. A., Lomax, B. H., Bomfleur, B., Kent, M. S., Fraser, W. T., & Jardine, P. E. (2023) · Science Advances · doi:10.1126/sciadv.abo6102 · Cited by 40

Climate and biotic evolution during the Permian-Triassic transition in the temperate Northern Hemisphere, Kuznetsk Basin, Siberia, Russia

Davydov, V. I., Karasev, E., Nurgalieva, N. G., Schmitz, M. D., Будников, И. В., Biakov, A. S., Kuzina, D. M., Silantiev, V. V., Urazaeva, M. N., Zharinova, V. V., et al. (2021) · Palaeogeography Palaeoclimatology Palaeoecology · doi:10.1016/j.palaeo.2021.110432 · Cited by 40

Early and late phases of the Permian–Triassic mass extinction marked by different atmospheric CO2 regimes

Shen, J., Zhang, Y., Yang, H., Xie, S., & Pearson, A. (2022) · Nature Geoscience · doi:10.1038/s41561-022-01034-w · Cited by 40

Groundfish biodiversity change in northeastern Pacific waters under projected warming and deoxygenation

Thompson, P. L., Nephin, J., Davies, S. C., Park, A. E., Lyons, D. A., Rooper, C. N., Peña, M. A., Christian, J. R., Hunter, K. L., Rubidge, E. M., et al. (2023) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2022.0191 · Cited by 37

Migration controls extinction and survival patterns of foraminifers during the Permian-Triassic crisis in South China

Liu, X., Song, H., Bond, D. P. G., Tong, J., & Benton, M. J. (2020) · Earth-Science Reviews · doi:10.1016/j.earscirev.2020.103329 · Cited by 39

Whale sharks increase swimming effort while filter feeding, but appear to maintain high foraging efficiencies

Cade, D. E., Levenson, J. J., Cooper, R. E., de la Parra, R., Webb, D. H., & Dove, A. D. M. (2020) · Journal of Experimental Biology · doi:10.1242/jeb.224402 · Cited by 35

New Middle–Late Permian Paleomagnetic and Geochronological Results From Inner Mongolia and their Paleogeographic Implications

Ren, Q., Zhang, S., Gao, Y., Zhao, H., Wu, H., Yang, T., & Li, H. (2020) · Journal of Geophysical Research Solid Earth · doi:10.1029/2019jb019114 · Cited by 35

Extinction risk controlled by interaction of long-term and short-term climate change

Mathes, G., van Dijk, J. P., Kiessling, W., & Steinbauer, M. J. (2021) · Nature Ecology & Evolution · doi:10.1038/s41559-020-01377-w · Cited by 36

Coculture of the Pacific white shrimp Litopenaeus vannamei and the macroalga Ulva linza enhances their growth rates and functional properties

Gao, G., Gao, L., Fu, Q., Li, X., & Xu, J. (2022) · Journal of Cleaner Production · doi:10.1016/j.jclepro.2022.131407 · Cited by 35

Strong Habitat Compression by Extreme Shoaling Events of Hypoxic Waters in the Eastern Pacific

Köhn, E. E., Münnich, M., Vogt, M., Desmet, F., & Gruber, N. (2022) · Journal of Geophysical Research Oceans · doi:10.1029/2022jc018429 · Cited by 39

Gradual warming prior to the end‐Permian mass extinction

Gliwa, J., Wiedenbeck, M., Schobben, M., Ullmann, C. V., Kiessling, W., Ghaderi, A., Struck, U., & Korn, D. (2022) · Palaeontology · doi:10.1111/pala.12621 · Cited by 33

Irreversible loss in marine ecosystem habitability after a temperature overshoot

Santana‐Falcón, Y., Yamamoto, A., Lenton, A. A., JONES, C. D., Burger, F. A., John, J. G., Tjiputra, J. F., Schwinger, J., Kawamiya, M., Frölicher, T. L., et al. (2023) · Communications Earth & Environment · doi:10.1038/s43247-023-01002-1 · Cited by 44

Marine siliceous ecosystem decline led to sustained anomalous Early Triassic warmth

Isson, T. T., Zhang, S., Lau, K., Rauzi, S., Tosca, N. J., Penman, D. E., & Planavsky, N. J. (2022) · Nature Communications · doi:10.1038/s41467-022-31128-3 · Cited by 33

Different drivers, common mechanism; the distribution of a reef fish is restricted by local-scale oxygen and temperature constraints on aerobic metabolism

Duncan, M. I., James, N. C., Potts, W. M., & Bates, A. E. (2020) · Conservation Physiology · doi:10.1093/conphys/coaa090 · Cited by 34

Biotic and Abiotic Controls on the Phanerozoic History of Marine Animal Biodiversity

Bush, A. M., & Payne, J. L. (2021) · Annual Review of Ecology Evolution and Systematics · doi:10.1146/annurev-ecolsys-012021-035131 · Cited by 36

The great catastrophe: causes of the Permo-Triassic marine mass extinction

Wignall, P. B., & Bond, D. P. G. (2023) · National Science Review · doi:10.1093/nsr/nwad273 · Cited by 30

Oxygen rise in the tropical upper ocean during the Paleocene-Eocene Thermal Maximum

Moretti, S., Auderset, A., Deutsch, C. A., Schmitz, R., Gerber, L., Thomas, E., Luciani, V., Petrizzo, M. R., Schiebel, R., Tripati, A., et al. (2024) · Science · doi:10.1126/science.adh4893 · Cited by 34

Coupled changes in pH, temperature, and dissolved oxygen impact the physiology and ecology of herbivorous kelp forest grazers

Donham, E. M., Strope, L., Hamilton, S. L., & Kroeker, K. J. (2022) · Global Change Biology · doi:10.1111/gcb.16125 · Cited by 33

Metabolic tradeoffs control biodiversity gradients through geological time

Boag, T. H., Gearty, W., & Stockey, R. (2021) · Current Biology · doi:10.1016/j.cub.2021.04.021 · Cited by 32

Size variations in foraminifers from the early Permian to the Late Triassic: implications for the Guadalupian–Lopingian and the Permian–Triassic mass extinctions

Feng, Y., Song, H., & Bond, D. P. G. (2020) · Paleobiology · doi:10.1017/pab.2020.37 · Cited by 28

Implications of giant ooids for the carbonate chemistry of Early Triassic seawater

Li, X., Trower, E. J., Lehrmann, D. J., Minzoni, M., Kelley, B. M., Schaal, E. K., Altıner, D., Yu, M., & Payne, J. L. (2020) · Geology · doi:10.1130/g47655.1 · Cited by 27

What causes mass extinctions? Large asteroid/comet impacts, flood-basalt volcanism, and ocean anoxia—Correlations and cycles

Rampino, M. R., Caldeira, K., & Prokoph, A. (2019) · Geological Society of America eBooks · doi:10.1130/2019.2542(14 · Cited by 27

Advancing statistical models to reveal the effect of dissolved oxygen on the spatial distribution of marine taxa using thresholds and a physiologically based index

Essington, T. E., Anderson, S. C., Barnett, L. A. K., Berger, H. M., Siedlecki, S. A., & Ward, E. J. (2022) · Ecography · doi:10.1111/ecog.06249 · Cited by 27

Taphonomy of drought afflicted tetrapods in the Early Triassic Karoo Basin, South Africa

Smith, R. M. H., Botha, J., & Viglietti, P. A. (2022) · Palaeogeography Palaeoclimatology Palaeoecology · doi:10.1016/j.palaeo.2022.111207 · Cited by 27

Using the Fossil Record to Understand Extinction Risk and Inform Marine Conservation in a Changing World

Finnegan, S., Harnik, P. G., Lockwood, R., Lotze, H. K., McClenachan, L., & Kahanamoku, S. S. (2023) · Annual Review of Marine Science · doi:10.1146/annurev-marine-021723-095235 · Cited by 28

Response of Siliceous Marine Organisms to the Permian‐Triassic Climate Crisis Based on New Findings From Central Spitsbergen, Svalbard

Foster, W. J., Asatryan, G., Rauzi, S., Botting, J. P., Buchwald, S. Z., Lazarus, D., Isson, T. T., Renaudie, J., & Kiessling, W. (2023) · Paleoceanography and Paleoclimatology · doi:10.1029/2023pa004766 · Cited by 26

Biological sensitivities to high‐resolution climate change projections in the California current marine ecosystem

Sunday, J., Howard, E., Siedlecki, S., Pilcher, D., Deutsch, C., MacCready, P., Newton, J., & Klinger, T. (2022) · Global Change Biology · doi:10.1111/gcb.16317 · Cited by 16

What the geological past can tell us about the future of the ocean’s twilight zone

Crichton, K. A., Wilson, J. D., Ridgwell, A., Boscolo-Galazzo, F., John, E. H., Wade, B. S., & Pearson, P. N. (2023) · Nature Communications · doi:10.1038/s41467-023-37781-6 · Cited by 23

Drivers of the “Great Dying”

VIGNIERI, S. N. (2018) · Science · doi:10.1126/science.362.6419.1124-n

Differences in physiological tolerance to global warming caused the Permian–Triassic transition between the Paleozoic and Modern faunas

Marquez, J. A., Penn, J. L., Stockey, R., Boag, T. H., Duncan, M. I., McClure, K. N., Matsumoto, K., Ashing-Giwa, K. F., Noll, C. P., Deutsch, C. A., et al. (2026) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2533086123 · Cited by 1

Global warming blamed for Earth’s largest mass extinction

Penn, J. L. (2019) · TheScienceBreaker · doi:10.25250/thescbr.brk277

Thermal and Nutrient Stress Drove Permian-Triassic Marine ExtinctionsPreprint

Foster, W. J., Frank, A. B., Li, Q., Danise, S., Wang, X., & Peckmann, J. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.09.08.556797 · Cited by 1

Ecological recovery dynamics of the benthic and pelagic fauna in response to extreme temperature events and low oxygen environments developed during the early Triassic

Pietsch, C. (2015) · University of Southern California Digital Library · doi:10.25549/usctheses-c3-627058 · Cited by 1