Frölicher, T. L., Fischer, E. M. & Gruber, N. Marine heatwaves under global warming. Nature 560, 360–364 (2018).
Kwiatkowski, L. & Orr, J. C. Diverging seasonal extremes for ocean acidification during the twenty-first centuryr. Nat. Clim. Chang. 8, 141–145 (2018).
Bates, A. E. et al. Biologists ignore ocean weather at their peril. Nature 560, 299–301 (2018).
Jentsch, A., Kreyling, J. & Beierkuhnlein, C. A new generation of climate-change experiments: Events, not trends. Front. Ecol. Environ. 5, 365–374 (2007).
Heron, S. F., Maynard, J. A., Van Hooidonk, R. & Eakin, C. M. Warming Trends and Bleaching Stress of the World’s Coral Reefs 1985–2012. Sci. Rep. 6, 1–14 (2016).
Grantham, B. A. et al. Upwelling-driven nearshore hypoxia signals ecosystem and oceanographic changes in the northeast Pacific. Nature 429, 749–754 (2004).
Vaquer-Sunyer, R. & Duarte, C. M. Thresholds of hypoxia for marine biodiversity. Proc. Natl. Acad. Sci. 105, 15452–15457 (2008).
Low, N. H. N. & Micheli, F. Lethal and functional thresholds of hypoxia in two key benthic grazers. Mar. Ecol. Prog. Ser. 594, 165–173 (2018).
Somero, G. N. Thermal physiology and vertical zonation of intertidal animals: Optima, limits, and costs of living. Integr. Comp. Biol. 42, 780–789 (2002).
Somero, G. N. Comparative physiology: a “crystal ball” for predicting consequences of global change. Am. J. Physiol. Regul. Integr. Comp. Physiol. 301, R1–R14 (2011).
Sanford, E. Regulation of keystone predation by small changes in ocean temperature. Science. 283, 2095–2097 (1999).
Sanford, E. Water temperature, predation, and the neglected role of physiological rate effects in rocky intertidal communities. Integr. Comp. Biol. 42, 881–891 (2002).
Kroeker, K. J., Micheli, F. & Gambi, M. C. Ocean acidification causes ecosystem shifts via altered competitive interactions. Nat. Clim. Chang. 3, 156–159 (2013).
Dufault, A. M., Cumbo, V. R., Fan, T.-Y. & Edmunds, P. J. Effects of diurnally oscillating pCO2 on the calcification and survival of coral recruits. Proc. R. Soc. B Biol. Sci. 279, 2951–2958 (2012).
Frieder, C. A., Gonzalez, J. P., Bockmon, E. E., Navarro, M. O. & Levin, L. A. Can variable pH and low oxygen moderate ocean acidification outcomes for mussel larvae? Glob. Chang. Biol. 20, 754–764 (2014).
Oliver, T. A. & Palumbi, S. R. Do fluctuating temperature environments elevate coral thermal tolerance? Coral Reefs 30, 429–440 (2011).
Mangan, S., Urbina, M. A., Findlay, H. S., Wilson, R. W. & Lewis, C. Fluctuating seawater pH/pCO2 regimes are more energetically expensive than static pH/pCO2 levels in the mussel Mytilus edulis. Proc. R. Soc. B Biol. Sci. 284, 20171642 (2017).
Chan, F. et al. Persistent spatial structuring of coastal ocean acidification in the California Current System. Sci. Rep. 7, 1–8 (2017).
Leary, P. R. et al. “Internal tide pools” prolong kelp forest hypoxic events. Limnol. Oceanogr. 62, 2864–2878 (2017).
Safaie, A. et al. High frequency temperature variability reduces the risk of coral bleaching. Nat. Commun. 9, 1–12 (2018).
Woodson, C. B. et al. Harnessing marine microclimates for climate change adaptation and marine conservation. Conserv. Lett. 1–9, https://doi.org/10.1111/conl.12609 (2018).
Boch, C. A. et al. Local oceanographic variability influences the performance of juvenile abalone under climate change. Sci. Rep. 1–12, https://doi.org/10.1038/s41598-018-23746-z (2018).
Kim, T. W., Barry, J. P. & Micheli, F. The effects of intermittent exposure to low-pH and low-oxygen conditions on survival and growth of juvenile red abalone. Biogeosciences 10, 7255–7262 (2013).
Breitburg, D. et al. Declining oxygen in the global ocean and coastal waters. Science. 359, eaam7240 (2018).
Chan, F. et al. Emergence of anoxia in the California Current Large Marine Ecosystem. Science 319, 920 (2008).
Booth, J. A. T. et al. Natural intrusions of hypoxic, low pH water into nearshore marine environments on the California coast. Cont. Shelf Res. 45, 108–115 (2012).
Bakun, A., Field, D. B., Redondo-Rodriguez, A. & Weeks, S. J. Greenhouse gas, upwelling-favorable winds, and the future of coastal ocean upwelling ecosystems. Glob. Chang. Biol. 16, 1213–1228 (2010).
Sydeman, W. J. et al. Climate change and wind intensification in coastal upwelling ecosystems. Science. 345, 77–80 (2014).
Keeling, R. E., Körtzinger, A. & Gruber, N. Ocean deoxygenation in a warming world. Ann. Rev. Mar. Sci. 2, 199–229 (2010).
Micheli, F. et al. Evidence that marine reserves enhance resilience to climatic impacts. PLoS One 7, e40832 (2012).
Booth, J. A. T. et al. Patterns and potential drivers of declining oxygen content along the southern California coast. Limnol. Oceanogr. 59, 1127–1138 (2014).
Watanabe, J. M. & Harrold, C. Destructive grazing by sea urchins Strongylocentrotus spp. in a central California kelp forest: potential roles of recruitment, depth, and predation. Mar. Ecol. Prog. Ser. 71, 125–141 (1991).
Estes, J. A. & Duggins, D. O. Sea otters and kelp forests in Alaska: Generality and variation in a community ecological paradigm. Ecol. Monogr. 65, 75–100 (1995).
Beas-Luna, R. & Ladah, L. B. Latitudinal, seasonal, and small-scale spatial differences of the giant kelp, Macrocystis pyrifera, and an herbivore at their southern range limit in the northern hemisphere. Bot. Mar. 57, 73–83 (2014).
Rogers-Bennett, L. & Catton, C. A. Marine heat wave and multiple stressors tip bull kelp forest to sea urchin barrens. Sci. Rep. 9, 15050 (2019).
Beas-Luna, R. et al. An online database for informing ecological network models: http://kelpforest.ucsc.edu. PLoS One 9, e109356 (2014).
Bickel, T. O. & Perrett, C. Precise determination of aquatic plant wet mass using a salad spinner. Can. J. Fish. Aquat. Sci. 73, 1–4 (2016).
Gonor, J. J. Reproductive cycles in oregon populations of the echinoid, Strongylocentrotus purpuratus (Stimpson). I. Annual gonad growth and ovarian gametogenic cycles. J. Exp. Mar. Bio. Ecol. 12, 45–64 (1973).
Kenner, M. & Lares, M. Size at first reproduction of the sea urchin Strongylocentrotus purpuratus in a central California kelp forest. Mar. Ecol. Prog. Ser. 76, 303–306 (1991).
Reinardy, H. C., Emerson, C. E., Manley, J. M. & Bodnar, A. G. Tissue regeneration and biomineralization in sea urchins: Role of Notch signaling and presence of stem cell markers. PLoS One 10, 1–15 (2015).
Giese, A. C., Farmanfarmaian, A., Hilden, S. & Doezema, P. Respiration during the reproductive cycle in the sea urchin, Strongylocentrotus purpuratus. Biol. Bull. 130, 192–201 (1966).
Webster, S. K. & Giese, A. C. Oxygen consumption of the purple sea urchin with special reference to the reproductive cycle. Biol. Bull. 148, 165–180 (1975).
Siikavuopio, S. I., Dale, T., Mortensen, A. & Foss, A. Effects of hypoxia on feed intake and gonad growth in the green sea urchin, Strongylocentrotus droebachiensis. Aquaculture 266, 112–116 (2007).
Chabot, D. & Claireaux, G. Environmental hypoxia as a metabolic constraint on fish: The case of Atlantic cod, Gadus morhua. Mar. Pollut. Bull. 57, 287–294 (2008).
Thomas, P., Rahman, M. S., Picha, M. E. & Tan, W. Impaired gamete production and viability in Atlantic croaker collected throughout the 20,000 km2 hypoxic region in the northern Gulf of Mexico. Mar. Pollut. Bull. 101, 182–192 (2015).
Jeppesen, R. et al. Effects of hypoxia on fish survival and oyster growth in a highly eutrophic estuary. Estuaries and Coasts 41, 299–299 (2018).
Lundquist, C. J. & Botsford, L. W. Estimating larval production of a broadcast spawner: the influence of density, aggregation, and the fertilization Allee effect. Can. J. Fish. Aquat. Sci. 68, 30–42 (2011).
Strathmann, R. R. The role of spines in preventing structural damage to echinoid tests. Paleobiology 7, 400–406 (1981).
Steneck, R. S. et al. Kelp forest ecosystems: biodiversity, stability, resilience and future. Environ. Conserv. 29, 436–459 (2002).
Ling, S. D. et al. Global regime shift dynamics of catastrophic sea urchin overgrazing. Philos. Trans. R. Soc. B 307 (2014).
Tegner, M. J. & Levin, L. A. Spiny lobsters and sea urchins: Analysis of a predator-prey interaction. J. Exp. Mar. Bio. Ecol. 73, 125–150 (1983).
Frieder, C. A., Nam, S. H., Martz, T. R. & Levin, L. A. High temporal and spatial variability of dissolved oxygen and pH in a nearshore California kelp forest. Biogeosciences 9, 3917–3930 (2012).
Steen, J. B. Comparative aspects of the respiratory gas exchange of sea urchins. Acta Physiol. Scand. 63, 164–170 (1965).
Gunderson, A. R., Armstrong, E. J. & Stillman, J. H. Multiple stressors in a changing world: The need for an improved perspective on physiological responses to the dynamic marine environment. Ann. Rev. Mar. Sci. 8, 357–378 (2016).
Hofmann, G. E. et al. The effect of ocean acidification on calcifying organisms in marine ecosystems: An organism-to-ecosystem perspective. Annu. Rev. Ecol. Evol. Syst. 41, 127–147 (2010).
Kurihara, H., Yin, R., Nishihara, G. N., Soyano, K. & Ishimatsu, A. Effect of ocean acidification on growth, gonad development and physiology of the sea urchin Hemicentrotus pulcherrimus. Aquat. Biol. 18, 281–292 (2013).
Burnell, O. W., Russell, B. D., Irving, A. D. & Connell, S. D. Eutrophication offsets increased sea urchin grazing on seagrass aused by ocean warming and acidification. Mar. Ecol. Prog. Ser. 485, 37–46 (2013).
Carey, N., Harianto, J. & Byrne, M. Sea urchins in a high CO2 world: partitioned effects of body-size, ocean warming and acidification on metabolic rate. J. Exp. Biol. 219, 1178–1186 (2016).
Crain, C. M., Kroeker, K. & Halpern, B. S. Interactive and cumulative effects of multiple human stressors in marine systems. Ecol. Lett. 11, 1304–1315 (2008).
Darling, E. S. & Côté, I. M. Quantifying the evidence for ecological synergies. Ecol. Lett. 11, 1278–1286 (2008).
Riebesell, U. & Gattuso, J.-P. Lessons learned from ocean acidification research. Nat. Clim. Chang. 5, 12–14 (2015).
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