Biological thresholds for marine carbon dioxide removal (mCDR): the effect of changes in carbonate chemistry
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Abstract. Marine carbon dioxide removal (mCDR) encompasses a variety of approaches to actively remove CO2 from the atmosphere, which, given current and projected emissions, is necessary to keep global average temperature increases to less than 2 °C. In addition to the removal of CO2 from the atmosphere, mCDR projects would have effects on the marine environment, including changes in ocean carbonate chemistry. These changes in carbonate chemistry can affect marine organisms through multiple physiological pathways. Although research on the effects of ocean acidification over the last fifteen years has advanced understanding of the effects of low pH/high CO2 conditions on marine organisms, much less is known about organismal response to the high pH/low CO2 or high alkalinity conditions that can be generated by some mCDR methods. We created a database of available information on marine species response to the carbonate chemistry conditions that can be generated by mCDR with a focus on identifying carbonate chemistry thresholds at which biological responses occur. The database contains 310 studies, from which we estimated 276 thresholds. In addition to all mCDR studies available to date, we reviewed studies not explicitly designed to address mCDR. These studies used natural and artificially manipulated variations in carbonate chemistry, including increasing pH and alkalinity, to explore basic physiological and biological responses as well as approaches to mitigate ocean acidification. In analyzing the database, we considered a variety of biological responses, both positive and negative, and considered sensitivity by taxa, exposure duration, treatment method and other factors. Using practical definitions of a threshold, including one based on the treatment level leading to the first statistically significant biological response, we describe the distribution of pH and alkalinity threshold values. The data reveal a high tolerance for high pH (>12) and high alkalinity for some species responses under some experimental conditions, but negative response to experimental conditions only slightly above ambient (pH 8.3) for other species responses. A positive effect of pH above ambient levels was observed in six cases, just 3 % of the total. We summarize results by presenting the distributions of threshold estimates collected from individual studies. The uncertainty and variation in organismal response represents a challenge for the development of management guidelines for the developing mCDR industry. Building on our review of existing studies, we suggest several paths forward for improved biological threshold estimates for mCDR-relevant carbonate chemistry conditions.
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Existing studies report variable biological responses, ranging from substantial shifts in plankton biomass and community structure to negligible ecological effects under different OAE scenarios.
“Existing studies report variable biological responses, ranging from substantial shifts in plankton biomass and community structure to negligible ecological effects under different OAE scenarios (Guo et al., 2025; McElhany et al., 2026; Sánchez et al., 2024; Xin et al., 2024).”
From Biogeochemical responses to ocean alkalinity enhancement in the North China Sea (2026) · cites this paper as McElhany et al., 2026
Section 3.2.1 (page unavailable) reports variable phytoplankton responses under OAE conditions, including a 30% decline in primary production, shifts in cell size and diatom selection, and neutral effects. It also reports no significant change in the overall planktonic community under mild alkalinity increases. These passages support the range of responses and community changes, but do not establish the claimed substantial shifts in plankton biomass. (LLM, conf=0.82)
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- 850 851 https://doi.org/10.5194/egusphere-2026-1597 Preprint. Discussion started: 26 March 2026 c Author(s) 2026. CC BY 4.0 License. https://doi.org/10.5194/egusphere-2026-1597 Preprint. Discussion started: 26 March 2026 c Author(s) 2026. CC BY 4.0 License. https://doi.org/10.5194/egusphere-2026-1597 Preprint. Discussion started: 26 March 2026 c Author(s) 2026. CC BY 4.0 License. Silverman, J., Wolfe, K., Zhu, K., and Caldeira, K.: Reversal of ocean acidification enhances net coral reef calcification, Nature, 531, 362-365, https://doi.org/10.1038/nature17155, 2016. · DOI
- Andersson, A. J. and Gledhill, D.: Ocean acidification and coral reefs: effects on breakdown, dissolution, and net ecosystem calcification, Annual Review of Marine Science, 5, 321-348, https://doi.org/10.1146/annurev-marine-121211-172241, 2013. · DOI
- Aquino De Souza, R., Tyler, P., and Hawkins, S. J.: Artificial oocyte maturation in Patella depressa and Patella vulgata using NaOH-alkalinized seawater, Marine Biology Research, 5, 503-510, https://doi.org/10.1080/17451000802603645, 2009. · DOI
- Arrieta, J. M., Weinbauer, M. G., Lute, C., and Herndl, G. J.: Response of bacterioplankton to iron fertilization in the Southern Ocean, Limnology & Oceanography, 49, 799-808, https://doi.org/10.4319/lo.2004.49.3.0799, 2004. · DOI
- Assmy, P., Henjes, J., Klaas, C., and Smetacek, V.: Mechanisms determining species dominance in a phytoplankton bloom induced by the iron fertilization experiment EisenEx in the Southern Ocean, Deep Sea Research Part I: Oceanographic Research Papers, 54, 340-362, https://doi.org/10.1016/j.dsr.2006.12.005, 2007. · DOI
- de Baar, H. J. W., Boyd, P. W., Coale, K. H., Landry, M. R., Tsuda, A., Assmy, P., Bakker, D. C. E., Bozec, Y., Barber, R. T., Brzezinski, M. A., Buesseler, K. O., Boyé, M., Croot, P. L., Gervais, F., Gorbunov, M. Y., Harrison, P. J., Hiscock, W. T., Laan, P., Lancelot, C., Law, C. S., Levasseur, M., Marchetti, A., Millero, F. J., Nishioka, J., Nojiri, Y., van Oijen, T., Riebesell, U., Rijkenberg, M. J. A., Saito, H., Takeda, S., Timmermans, K. R., Veldhuis, M. J. W., Waite, A. M., and Wong, C.-S.: Synthesis of iron fertilization experiments: From the Iron Age in the Age of Enlightenment, Journal of Geophysical Research: Oceans, 110, https://doi.org/10.1029/2004JC002601, 2005. · DOI
- Bach, L. T.: Reconsidering the role of carbonate ion concentration in calcification by marine organisms, Biogeosciences, 12, 4939-4951, https://doi.org/10.5194/bg-12-4939-2015, 2015. · DOI
- Bach, L. T. and Boyd, P. W.: Seeking natural analogs to fast-forward the assessment of marine CO 2 removal, Proc. Natl. Acad. Sci. U.S.A., 118, e2106147118, https://doi.org/10.1073/pnas.2106147118, 2021. · DOI
- Bach, L. T., Mackinder, L. C. M., Schulz, K. G., Wheeler, G., Schroeder, D. C., Brownlee, C., and Riebesell, U.: Dissecting the impact of CO 2 and pH on the mechanisms of photosynthesis and calcification https://doi.org/10.5194/egusphere-2026-1597 Preprint. Discussion started: 26 March 2026 c Author(s) 2026. CC BY 4.0 License. in the coccolithophore Emiliania huxleyi , New Phytologist, 199, 121-134, https://doi.org/10.1111/nph.12225, 2013. · DOI
- Bach, L. T., Tamsitt, V., Gower, J., Hurd, C. L., Raven, J. A., and Boyd, P. W.: Testing the climate intervention potential of ocean afforestation using the Great Atlantic Sargassum Belt, Nat Commun, 12, 2556, https://doi.org/10.1038/s41467-021-22837-2, 2021. · DOI
- Batten, S. D. and Gower, J. F. R.: Did the iron fertilization near Haida Gwaii in 2012 affect the pelagic lower trophic level ecosystem?, Journal of Plankton Research, 36, 925-932, https://doi.org/10.1093/plankt/fbu049, 2014. · DOI
- Baumann, H.: Experimental assessments of marine species sensitivities to ocean acidification and co-stressors: how far have we come?, Can. J. Zool., 97, 399-408, https://doi.org/10.1139/cjz-2018-0198, 2019. · DOI
- Bednaršek, N., van de Mortel, H., Pelletier, G., García-Reyes, M., Feely, R. A., and Dickson, A. G.: Assessment framework to predict sensitivity of marine calcifiers to ocean alkalinity enhancement - identification of biological thresholds and importance of precautionary principle, Biogeosciences, 22, 473-498, https://doi.org/10.5194/bg-22-473-2025, 2025. · DOI
- Bhaumik, A., Faucher, G., Henning, M., Meunier, C. L., and Boersma, M.: Prey dynamics as a buffer: enhancing copepod resilience to ocean alkalinity enhancement, Environ. Res. Lett., 20, 024058, https://doi.org/10.1088/1748-9326/adaa8c, 2025. · DOI
- Björk, M., Axelsson, L., and Beer, S.: Why is Ulva intestinalis the only macroalga inhabiting isolated rockpools along the Swedish Atlantic coast?, Marine Ecology Progress Series, 284, 109-116, https://doi.org/10.3354/meps284109, 2004. · DOI
- Blain, S., Quéguiner, B., Armand, L., Belviso, S., Bombled, B., Bopp, L., Bowie, A., Brunet, C., Brussaard, C., Carlotti, F., Christaki, U., Corbière, A., Durand, I., Ebersbach, F., Fuda, J.-L., Garcia, N., Gerringa, L., Griffiths, B., Guigue, C., Guillerm, C., Jacquet, S., Jeandel, C., Laan, P., Lefèvre, D., Lo Monaco, C., Malits, A., Mosseri, J., Obernosterer, I., Park, Y.-H., Picheral, M., Pondaven, P., Remenyi, T., Sandroni, V., Sarthou, G., Savoye, N., Scouarnec, L., Souhaut, M., Thuiller, D., Timmermans, K., Trull, T., Uitz, J., Van Beek, P., Veldhuis, M., Vincent, D., Viollier, E., Vong, L., and Wagener, T.: Effect of natural iron fertilization on carbon sequestration in the Southern Ocean, Nature, 446, 1070-1074, https://doi.org/10.1038/nature05700, 2007. · DOI
- Blain, S., Sarthou, G., and Laan, P.: Distribution of dissolved iron during the natural iron-fertilization experiment KEOPS (Kerguelen Plateau, Southern Ocean), Deep Sea Research Part II: Topical Studies in Oceanography, 55, 594-605, https://doi.org/10.1016/j.dsr2.2007.12.028, 2008. · DOI
- Borenstein, M., Hedges, L. V., Higgins, J. P. T., and Rothstein, H. R.: Introduction to Meta-Analysis, https://doi.org/DOI:10.1002/9780470743386, 2021. · DOI
- Brauner, C. J. and Baker, D. W.: Patterns of acid-base regulation during exposure to hypercarbia in fishes, in: Cardio-Respiratory Control in Vertebrates: Comparative and Evolutionary Aspects, edited by: Glass, M. L. and Wood, S. C., Springer, Berlin, Heidelberg, 43-63, https://doi.org/10.1007/978-3-540-93985-6_3, 2009. · DOI
- Brooks, S. J., Georgantzopoulou, A., Johansen, J. T., and Mengede, M.: Determining the risk of calcium oxide (CaO) particle exposure to marine organisms, Marine Environmental Research, 156, 104917, https://doi.org/10.1016/j.marenvres.2020.104917, 2020. · DOI
- Brownell, C. L.: Water quality requirements for first-feeding in marine fish larvae. II. pH, oxygen, and carbon dioxide, Journal of Experimental Marine Biology and Ecology, 44, 285-298, https://doi.org/10.1016/0022-0981(80)90159-8, 1980. · DOI
- Brussaard, C., Gast, G., van Duyl, F., and Amann, R.: Impact of phytoplankton bloom magnitude on a pelagic microbial food web, Marine Ecology Progress Series, 144, 211-221, https://doi.org/10.3354/meps144211, 1996. · DOI
- Calabrese, A. and Davis, H. C.: The pH tolerance of embryos and larvae of Mercenaria mercenaria and Crassostrea virginica , The Biological Bulletin, 131, 427-436, https://doi.org/10.2307/1539982, 1966. · DOI
- Camatti, E., Valsecchi, S., Caserini, S., Barbaccia, E., Santinelli, C., Basso, D., and Azzellino, A.: Short-term impact assessment of ocean liming: A copepod exposure test, Marine Pollution Bulletin, 198, 115833, https://doi.org/10.1016/j.marpolbul.2023.115833, 2024. · DOI
- Cañizares, J. M., Castejón, D., Haroun, R., Nogueira, N., and Andrade, C. A. P.: Enhancing oocyte maturation and fertilisation in the black-foot limpet Patella candei d′Orbigny, 1840 (Patellidae, Mollusca), Aquaculture Reports, 21, 100856, https://doi.org/10.1016/j.aqrep.2021.100856, 2021. · DOI
- Cañizares, J. M., Castejón, D., Haroun, R., Nogueira, N., and Andrade, C. A. P.: Corrigendum to "Enhancing oocyte maturation and fertilisation in the black-foot limpet Patella candei d′Orbigny, 1840 (Patellidae, Mollusca)" [Aquac. Rep. 21 (2021) 100856], Aquaculture Reports, 22, 100929, https://doi.org/10.1016/j.aqrep.2021.100929, 2022. · DOI
- Cao, L. and Caldeira, K.: Can ocean iron fertilization mitigate ocean acidification?: A letter, Climatic Change, 99, 303-311, https://doi.org/10.1007/s10584-010-9799-4, 2010. · DOI
- Carstensen, J. and Duarte, C. M.: Drivers of pH Variability in Coastal Ecosystems, Environ. Sci. Technol., 53, 4020-4029, https://doi.org/10.1021/acs.est.8b03655, 2019. · DOI
- Castejón, D., Cañizares, J. M., Nogueira, N., and Andrade, C. A. P.: Artificial maturation and larval production of the limpet Patella aspera Röding, 1798 (Patellogastropoda, Mollusca): Enhancing fertilization success of oocytes using NaOH-alkalinized seawater, Aquaculture Research, 52, 1904-1914, https://doi.org/10.1111/are.15039, 2021. · DOI
- Ciani, E., Stormoen, M., Antonsen, S. I., Nilsen, F., Jørgensen, E. H., and Komisarczuk, A. Z.: Optimization of calcium oxide treatment against salmon louse ( Lepeophtheirus salmonis ). A controlled laboratory study, Aquaculture Reports, 43, 102894, https://doi.org/10.1016/j.aqrep.2025.102894, 2025. · DOI
- Clements, J. C. and Chopin, T.: Ocean acidification and marine aquaculture in North America: potential impacts and mitigation strategies, Reviews in Aquaculture, 9, 326-341, https://doi.org/10.1111/raq.12140, 2017. · DOI
- Comeau, L. A., Sonier, R., Guyondet, T., Landry, T., Ramsay, A., and Davidson, J.: Behavioural response of bivalve molluscs to calcium hydroxide, Aquaculture, 466, 78-85, https://doi.org/10.1016/j.aquaculture.2016.09.045, 2017. · DOI
- Cooley, S., Schoeman, D., Bopp, L., Boyd, P., Donner, S., Ghebrehiwet, D. Y., Ito, S.-I., Kiessling, W., Martinetto, P., Ojea, E., Racault, M.-F., Rost, B., and Skern-Mauritzen, M.: Oceans and Coastal Ecosystems and Their Services, in: Climate Change 2022: Impacts, Adaptation and Vulnerability, edited by: Pörtner, H.-O., Roberts, D. C., Tignor, M., Poloczanska, E. S., Mintenbeck, K., Alegría, A., Craig, M., Langsdorf, S., Löschke, S., Möller, V., Okem, A., and Rama, B., Cambridge University Press, Cambridge, UK and New York, NY, USA, 379-550, 2022.
- Copping, A. and Hemery, L.: OES-Environmental 2020 State of the Science Report: Environmental Effects of Marine Renewable Energy Development Around the World. Report for Ocean Energy Systems (OES), https://doi.org/10.2172/1632878, 2020. · DOI
- Cornwall, C. E. and Hurd, C. L.: Experimental design in ocean acidification research: problems and solutions, ICES Journal of Marine Science, 73, 572-581, https://doi.org/10.1093/icesjms/fsv118, 2015. · DOI
- Cornwall, C. E. and Hurd, C. L.: Variability in the benefits of ocean acidification to photosynthetic rates of macroalgae without CO2-concentrating mechanisms, Mar Freshwater Res, 71, 275-280, https://doi.org/10.1071/MF19134, 2019. · DOI
- Cottingham, K. L., Lennon, J. T., and Brown, B. L.: Knowing when to draw the line: designing more informative ecological experiments, Frontiers in Ecology and the Environment, 3, 145-152, https://doi.org/10.1890/1540-9295(2005)003%5B0145:KWTDTL%5D2.0.CO;2, 2005. · DOI
- Crespi, B. J.: The evolution of maladaptation, Heredity, 84, 623-629, https://doi.org/10.1046/j.1365-2540.2000.00746.x, 2000. · DOI
- Cripps, G., Widdicombe, S., Spicer, J. I., and Findlay, H. S.: Biological impacts of enhanced alkalinity in Carcinus maenas , Mar. Pollut. Bull., 71, 190-198, https://doi.org/10.1016/j.marpolbul.2013.03.015, 2013. · DOI
- Daye, P. and Garside, E.: Lethal levels of pH for brook trout, Salvelinus fontinalis (Mitchill), Can. J. Zool., 53, 639-641, https://doi.org/10.1139/z75-077, 1975. · DOI
- Daye, P. G. and Garside, E. T.: Histopathologic changes in surficial tissues of brook trout, Salvelinus fontinalis (Mitchill), exposed to acute and chronic levels of pH, Can. J. Zool., 54, 2140-2155, https://doi.org/10.1139/z76-248, 1976. · DOI
- Daye, P. G. and Garside, E. T.: Development, survival, and structural alterations of embryos and alevins of Atlantic salmon, Salmo salar L., continuously exposed to alkaline levels of pH, from fertilization, Can. J. Zool., 58, 369-377, https://doi.org/10.1139/z80-047, 1980. · DOI
- Delacroix, S., Nystuen, T. J., Tobiesen, A. E. D., King, A. L., and Höglund, E.: Ocean alkalinity enhancement impacts: regrowth of marine microalgae in alkaline mineral concentrations simulating the initial concentrations after ship-based dispersions, Biogeosciences, 21, 3677-3690, https://doi.org/10.5194/bg-21-3677-2024, 2024. · DOI
- Dolliver, J. and O'Connor, N.: Whole system analysis is required to determine the fate of macroalgal carbon: a systematic review, Journal of Phycology, 58, 364-376, https://doi.org/10.1111/jpy.13251, 2022. · DOI
- Doney, S. C., Fabry, V. J., Feely, R. A., and Kleypas, J. A.: Ocean acidification: the other CO 2 problem, Annual review of marine science, 1, 169-192, 2009.
- Doney, S. C., Busch, D. S., Cooley, S. R., and Kroeker, K. J.: The Impacts of Ocean Acidification on Marine Ecosystems and Reliant Human Communities, Annual Review of Environment and Resources, 45, 83-112, https://doi.org/10.1146/annurev-environ-012320-083019, 2020. · DOI
- Doney, S. C., Wolfe, W. H., McKee, D. C., and Fuhrman, J. G.: The science, engineering, and validation of marine carbon dioxide removal and storage, Annual Review of Marine Science, https://doi.org/10.1146/annurev-marine-040523-014702, 2024. · DOI
- Duarte, C. M., Gattuso, J.-P., Hancke, K., Gundersen, H., Filbee-Dexter, K., Pedersen, M. F., Middelburg, J. J., Burrows, M. T., Krumhansl, K. A., Wernberg, T., Moore, P., Pessarrodona, A., Ørberg, S. B., Pinto, I. S., Assis, J., Queirós, A. M., Smale, D. A., Bekkby, T., Serrão, E. A., and Krause-Jensen, D.: Global estimates of the extent and production of macroalgal forests, Global Ecology and Biogeography, 31, 1422-1439, https://doi.org/10.1111/geb.13515, 2022. · DOI
- Dupont, S., Ortega-Martínez, O., and Thorndyke, M.: Impact of near-future ocean acidification on echinoderms, Ecotoxicology, 19, 449-462, https://doi.org/10.1007/s10646-010-0463-6, 2010. · DOI
- Dutkiewicz, S., Boyd, P. W., and Riebesell, U.: Exploring biogeochemical and ecological redundancy in phytoplankton communities in the global ocean, Global Change Biology, 27, 1196-1213, https://doi.org/10.1111/gcb.15493, 2021. · DOI
- Elskus, A. A., Ingersoll, C. G., Kemble, N. E., Echols, K. R., Brumbaugh, W. G., Henquinet, J. W., and Watten, B. J.: An evaluation of the residual toxicity and chemistry of a sodium hydroxide-based ballast water treatment system for freshwater ships, Environmental Toxicology and Chemistry, 34, 1405-1416, https://doi.org/10.1002/etc.2943, 2015. · DOI
- Esbaugh, A. J.: Physiological implications of ocean acidification for marine fish: emerging patterns and new insights, J Comp Physiol B, 188, 1-13, https://doi.org/10.1007/s00360-017-1105-6, 2018. · DOI
- Fan, D., Pan, L., Ma, S., and Dong, S.: Effects of salinity and pH on oxygen consumption rate and ammonia excretion rate in Sinonovacula constricta , Journal of Fishery Sciences of China, 9, 234-239, 2002.
- Fang, W., Wang, H., and Lai, Q.: Toxicity of carbonate-alkalinity and pH to larval Penaeus chinensi , Journal of Fishery Sciences of China, 7, 78-81, 2000.
- Faucher, G., Haunost, M., Paul, A. J., Tietz, A. U. C., and Riebesell, U.: Growth response of Emiliania huxleyi to ocean alkalinity enhancement, Biogeosciences, 22, 405-415, https://doi.org/10.5194/bg-22-405-2025, 2025. · DOI
- Ferderer, A., Chase, Z., Kennedy, F., Schulz, K. G., and Bach, L. T.: Assessing the influence of ocean alkalinity enhancement on a coastal phytoplankton community, Biogeosciences, 19, 5375-5399, https://doi.org/10.5194/bg-19-5375-2022, 2022. · DOI
- Ferderer, A., Schulz, K. G., Riebesell, U., Baker, K. G., Chase, Z., and Bach, L. T.: Investigating the effect of silicate-and calcium-based ocean alkalinity enhancement on diatom silicification, Biogeosciences, 21, 2777-2794, https://doi.org/10.5194/bg-21-2777-2024, 2024. · DOI
- Ferderer, A., Schulz, K. G., Willis, A., Baker, K. G., Chase, Z., and Bach, L. T.: Carbonate chemistry fitness landscapes inform diatom resilience to future perturbations, Science Advances, 11, eadu8024, https://doi.org/10.1126/sciadv.adu8024, 2025. · DOI
- Findlay, H. S., Feely, R. A., Jiang, L.-Q., Pelletier, G., and Bednaršek, N.: Ocean Acidification: Another Planetary Boundary Crossed, Global Change Biology, 31, e70238, https://doi.org/https://doi.org/10.1111/gcb.70238, 2025. · DOI
- Flipkens, G., Blust, R., and Town, R. M.: Deriving Nickel (Ni(II)) and Chromium (Cr(III)) Based Environmentally Safe Olivine Guidelines for Coastal Enhanced Silicate Weathering, Environ. Sci. Technol., 55, 12362-12371, https://doi.org/10.1021/acs.est.1c02974, 2021. · DOI
- Foldvik, A., Holthe, E., Bremset, G., and Solem, Ø.: Effects of Episodic Exposure to High-pH Water on Survival of Atlantic Salmon Eggs and Juveniles: Results from Laboratory and Field Studies, Environmental Toxicology and Chemistry, 41, 771-780, https://doi.org/10.1002/etc.5282, 2022. · DOI
- Foley, M. M., Martone, R. G., Fox, M. D., Kappel, C. V., Mease, L. A., Erickson, A. L., Halpern, B. S., Selkoe, K. A., Taylor, P., and Scarborough, C.: Using ecological thresholds to inform resource management:current options and future possibilities, Front. Mar. Sci., 2, https://doi.org/10.3389/fmars.2015.00095, 2015. · DOI
- Fuhrman, J., Bergero, C., Weber, M., Monteith, S., Wang, F. M., Clarens, A. F., Doney, S. C., Shobe, W., and McJeon, H.: Diverse carbon dioxide removal approaches could reduce impacts on the energy-water-land system, Nat. Clim. Chang., 13, 341-350, https://doi.org/10.1038/s41558-023-01604-9, 2023. · DOI
- Gately, J. A., Kim, S. M., Jin, B., Brzezinski, M. A., and Iglesias-Rodriguez, M. D.: Coccolithophores and diatoms resilient to ocean alkalinity enhancement: A glimpse of hope?, Science Advances, 9, eadg6066, https://doi.org/10.1126/sciadv.adg6066, 2023. · DOI
- Gilmour, K. M. and Perry, S. F.: Carbonic anhydrase and acid-base regulation in fish, J Exp Biol, 212, 1647-1661, https://doi.org/10.1242/jeb.029181, 2009. · DOI
- Gim, B.-M., Hong, S., Lee, J.-S., Kim, N.-H., Kwon, E.-M., Gil, J.-W., Lim, H.-H., Jeon, E.-C., and Khim, J. S.: Potential ecotoxicological effects of elevated bicarbonate ion concentrations on marine organisms, Environmental Pollution, 241, 194-199, https://doi.org/10.1016/j.envpol.2018.05.057, 2018. · DOI
- Goldenberg, S. U., Riebesell, U., Brüggemann, D., Börner, G., Sswat, M., Folkvord, A., Couret, M., Spjelkavik, S., Sánchez, N., Jaspers, C., and Moyano, M.: Early life stages of fish under ocean alkalinity enhancement in coastal plankton communities, Biogeosciences, 21, 4521-4532, https://doi.org/10.5194/bg-21-4521-2024, 2024. · DOI
- Grabb, K. C., Clevenger, S., Findlay, H. S., Gurney-Smith, H., Jewett, E. B., Kitch, G. D., McElhany, P., Paul, K., and Schumann, S.: The importance of engagement with fisheries, aquaculture, and Indigenous communities in the planning and implementation of marine carbon dioxide removal (mCDR), ICES J Mar Sci, 82, fsaf198, https://doi.org/10.1093/icesjms/fsaf198, 2025. · DOI
- Grabb, K. C., Wood, M., and McElhany, P.: An annotated literature database to support research on marine carbon dioxide removal (mCDR) and fisheries impacts., ICES Journal of Marine Science, 2026.
- Greiner, C. M., Klinger, T., Ruesink, J. L., Barber, J. S., and Horwith, M.: Habitat effects of macrophytes and shell on carbonate chemistry and juvenile clam recruitment, survival, and growth, Journal of Experimental Marine Biology and Ecology, 509, 8-15, https://doi.org/10.1016/j.jembe.2018.08.006, 2018. · DOI
- Guallart, J., Peña, J. B., Pérez-Larruscaín, J., Luque, A. A., and Templado, J.: Filling gaps: closing the life cycle of the endangered Mediterranean limpet Patella ferruginea Gmelin, 1791 (Gastropoda, Patellidae), Medit. Mar. Sci., https://doi.org/10.12681/mms.22508, 2020. · DOI
- Guo, J. A., Strzepek, R. F., Yuan, Z., Swadling, K. M., Townsend, A. T., Achterberg, E. P., Browning, T. J., and Bach, L. T.: Effects of ocean alkalinity enhancement on plankton in the Equatorial Pacific, Commun Earth Environ, 6, 270, https://doi.org/10.1038/s43247-025-02248-7, 2025. · DOI
- Gurney-Smith, H.: State of the knowledge on the interactions between marine carbon dioxide removal (mCDR) and fisheries, ICES Journal of Marine Science, 2026.
- Gutleben, J., Podell, S., Mizell, K., Sweeney, D., Neira, C., Levin, L. A., and Jensen, P. R.: Extremophile hotspots linked to containerized industrial waste dumping in a deep-sea basin, PNAS Nexus, 4, pgaf260, https://doi.org/10.1093/pnasnexus/pgaf260, 2025. · DOI
- Hall, J. A. and Safi, K.: The impact of in situ Fe fertilisation on the microbial food web in the Southern Ocean, Deep Sea Research Part II: Topical Studies in Oceanography, 48, 2591-2613, https://doi.org/10.1016/S0967-0645(01)00010-8, 2001. · DOI
- Halloran, P. R., Bell, T. G., Burt, W. J., Chu, S. N., Gill, S., Henderson, C., Ho, D. T., Kitidis, V., La Plante, E., Larrazabal, M., Loucaides, S., Pearce, C. R., Redding, T., Renforth, P., Taylor, F., Toome, K., Torres, R., and Watson, A.: Seawater carbonate chemistry based carbon dioxide removal: towards commonly agreed principles for carbon monitoring, reporting, and verification, Front. Clim., 7, https://doi.org/10.3389/fclim.2025.1487138, 2025. · DOI
- Hansen, B. W., Hansen, P. J., Nielsen, T. G., and Jepsen, P. M.: Effects of elevated pH on marine copepods in mass cultivation systems: practical implications, Journal of Plankton Research, 39, 984-993, https://doi.org/10.1093/plankt/fbx032, 2017. · DOI
- Harper, D. D., Farag, A. M., and Skaar, D.: Acute toxicity of sodium bicarbonate, a major component of coal bed natural gas produced waters, to 13 aquatic species as defined in the laboratory, Environmental Toxicology and Chemistry, 33, 525-531, https://doi.org/10.1002/etc.2452, 2014. · DOI
- Hartmann, J., Suitner, N., Lim, C., Schneider, J., Marín-Samper, L., Arístegui, J., Renforth, P., Taucher, J., and Riebesell, U.: Stability of alkalinity in ocean alkalinity enhancement (OAE) approaches - consequences for durability of CO 2 storage, Biogeosciences, 20, 781-802, https://doi.org/10.5194/bg-20-781-2023, 2023. · DOI
- He, M., Lai, Q., Yao, Z., Sui, Y., Lu, J., Gao, P., and Zhou, K.: Effects of pH and temperature on carbon budget of Sinonovacula constricta , Chinese Journal of Ecology, 36, 1014-1019, https://doi.org/10.13292/j.1000-4890.201704.004, 2017. · DOI
- Herfort, L., Thake, B., and Taubner, I.: Bicarbonate stimulation of calcification and photosynthesis in two hermatypic corals, Journal of Phycology, 44, 91-98, https://doi.org/10.1111/j.1529-8817.2007.00445.x, 2008. · DOI
- Hiddink, J. G., Valanko, S., Delargy, A. J., and van Denderen, P. D.: Setting thresholds for good ecosystem state in marine seabed systems and beyond, ICES Journal of Marine Science, 80, 698-709, https://doi.org/10.1093/icesjms/fsad035, 2023. · DOI
- Hitchin, B., Smith, S., Kröger, K., Jones, D., Jaeckel, A., Mestre, N., Ardron, J., Escobar, E., Van Der Grient, J., and Amaro, T.: Thresholds in deep-seabed mining: A primer for their development, Marine Policy, 149, 105505, https://doi.org/10.1016/j.marpol.2023.105505, 2023. · DOI
- Ho, D. T. and Bopp, L.: Marine carbon dioxide removal may be a future climate solution, Dialogues on Climate Change, 1, 56-62, https://doi.org/10.1177/29768659241293223, 2024. · DOI
- Hoffmann, L. J., Peeken, I., Lochte, K., Assmy, P., and Veldhuis, M.: Different reactions of Southern Ocean phytoplankton size classes to iron fertilization, Limnol. Oceanogr., 51, 1217-1229, https://doi.org/10.4319/lo.2006.51.3.1217, 2006. · DOI
- Hong, H., Shen, R., Zhang, F., Wen, Z., Chang, S., Lin, W., Kranz, S. A., Luo, Y.-W., Kao, S.-J., Morel, F. M. M., and Shi, D.: The complex effects of ocean acidification on the prominent N 2 -fixing cyanobacterium Trichodesmium, Science, 356, 527-531, https://doi.org/10.1126/science.aal2981, 2017. · DOI
- Hu, M. Y., Yan, J.-J., Petersen, I., Himmerkus, N., Bleich, M., and Stumpp, M.: A SLC4 family bicarbonate transporter is critical for intracellular pH regulation and biomineralization in sea urchin embryos, eLife, 7, e36600, https://doi.org/10.7554/eLife.36600, 2018. · DOI
- Huang, W., Cheng, C., Liu, J., Zhang, X., Ren, C., Jiang, X., Chen, T., Cheng, K., Li, H., and Hu, C.: Fine Mapping of the High-pH Tolerance and Growth Trait-Related Quantitative Trait Loci (QTLs) and Identification of the Candidate Genes in Pacific White Shrimp ( Litopenaeus vannamei ), Mar Biotechnol, 22, 1-18, https://doi.org/10.1007/s10126-019-09932-8, 2020. · DOI
- Huo, Z., Rbbani, Md. G., Cui, H., Xu, L., Yan, X., Fang, L., Wang, Y., and Yang, F.: Larval development, juvenile survival, and burrowing rate of geoduck clams ( Panopea japonica ) under different pH conditions, Aquacult Int, 27, 1331-1342, https://doi.org/10.1007/s10499-019-00389-z, 2019. · DOI
- Hutchins, D. A., Fu, F.-X., Yang, S.-C., John, S. G., Romaniello, S. J., Andrews, M. G., and Walworth, N. G.: Responses of globally important phytoplankton species to olivine dissolution products and implications for carbon dioxide removal via ocean alkalinity enhancement, Biogeosciences, 20, 4669-4682, https://doi.org/10.5194/bg-20-4669-2023, 2023. · DOI
- Iglesias-Rodriguez, M. D., Halloran, P. R., Rickaby, R. E. M., Hall, I. R., Colmenero-Hidalgo, E., Gittins, J. R., Green, D. R. H., Tyrrell, T., Gibbs, S. J., von Dassow, P., Rehm, E., Armbrust, E. V., and Boessenkool, K. P.: Phytoplankton calcification in a high-CO 2 world, Science, 320, 336-340, https://doi.org/10.1126/science.1154122, 2008. · DOI
- Iglesias-Rodríguez, M. D., Rickaby, R. E. M., Singh, A., and Gately, J. A.: Laboratory experiments in ocean alkalinity enhancement research, State of the Planet, 2-oae2023, 5, https://doi.org/10.5194/sp-2-oae2023-5-2023, 2023. · DOI
- IPCC: Summary for Policymakers In: Climate Change 2022: Mitigation of Climate Change Contribution of Working Group III to the Sixth Assessment Report of the Intergovernmental Panel on Climate Change, Cambridge University Press, Cambridge, UK and New York, NY, USA., 2022.
- Jankowska, E., Sclafani, M., Chang, B., Hayes, H., Cerrato, R., Fisher, N., Leach, C., Cole, D., Jackson, B., Gobler, C., Subhas, A., Hayden, M., and Andrews, M. G.: Limited impact on oysters in first-of-its-kind field trial of marine carbon dioxide removal (mCDR) strategy, https://doi.org/10.70212/cdrxiv.2025326.v1, 24 January 2025. · DOI
- Jewett, E., Grabb, K., Gurney-Smith, H., Kitch, G., McElhany, P., Methratta, E., Tiano, J., and Wood, M.: A fisheries-relevant research framework: scientific questions and methodologies to consider for assessing marine carbon dioxide removal (mCDR) approaches, ICES Journal of Marine Science, 2026.
- Jiang, L.-Q., Carter, B. R., Feely, R. A., Lauvset, S. K., and Olsen, A.: Surface ocean pH and buffer capacity: past, present and future, Sci Rep, 9, 18624, https://doi.org/10.1038/s41598-019-55039-4, 2019. · DOI
- Job, S., Sekadende, B., Yona, G., George, R., Lugendo, B. R., and Kimirei, I. A.: Effect of seagrass cover loss on seawater carbonate chemistry: Implications for the potential of seagrass meadows to mitigate https://doi.org/10.5194/egusphere-2026-1597 Preprint. Discussion started: 26 March 2026 c Author(s) 2026. CC BY 4.0 License. ocean acidification, Regional Studies in Marine Science, 60, 102816, https://doi.org/10.1016/j.rsma.2023.102816, 2023. · DOI
- Johnson, D. W.: Selection on offspring size and contemporary evolution under ocean acidification, Nat. Clim. Chang., 12, 757-760, https://doi.org/10.1038/s41558-022-01425-2, 2022. · DOI
- Johnson, M., van Doorn, E., Hilmi, N., Marandino, C., McDonald, N., Thomas, H., Allemand, D., Algarin, L. D., Lebleu, L., Ho, D. T., Oloyede, M., Safa, A., and Swarzenski, P.: Can coastal and marine carbon dioxide removal help to close the emissions gap? Scientific, legal, economic, and governance considerations, Elementa: Science of the Anthropocene, 12, 00071, https://doi.org/10.1525/elementa.2023.00071, 2024. · DOI
- Jones, K., Hemery, L. G., Ward, N. D., Regier, P. J., Ringham, M. C., and Eisaman, M. D.: Biological response of eelgrass epifauna, Taylor's Sea hare (Phyllaplysia taylori) and eelgrass isopod (Idotea resecata), to elevated ocean alkalinity, Biogeosciences, 22, 1615-1630, https://doi.org/10.5194/bg-22-1615-2025, 2025. · DOI
- Kelly, R. P., Erickson, A. L., Mease, L. A., Battista, W., Kittinger, J. N., and Fujita, R.: Embracing thresholds for better environmental management, Phil. Trans. R. Soc. B, 370, 20130276, https://doi.org/10.1098/rstb.2013.0276, 2015. · DOI
- Khangaonkar, T., Carter, B. R., Premathilake, L., Yun, S. K., Ni, W., Stoll, M. M., Ward, N. D., Hemery, L. G., Sanchez, C. T., Subban, C. V., Ringham, M. C., Eisaman, M. D., Pelman, T., Tallam, K., and Feely, R. A.: Mixing and dilution controls on marine CO 2 removal using alkalinity enhancement, Environ. Res. Lett., 19, 104039, https://doi.org/10.1088/1748-9326/ad7521, 2024. · DOI
- Kong, L., Abudu, A., Yang, L., Ye, M., Zhang, Y., Hong, Y., Chen, H., Li, G., Shi, G., and Tian, C.: Acute alkalinity stress triggers kidney histopathology, oxidative-immune dysregulation, and MAPK/TGF-β signaling pathways activation in Scatophagus argus , Aquaculture, 606, 742601, https://doi.org/10.1016/j.aquaculture.2025.742601, 2025. · DOI
- Kousoulas, K., Ferderer, A., Eriksen, R., and Bach, L. T.: Winners and losers under hydroxide-based ocean alkalinity enhancement in a Tasmanian plankton community, Journal of Phycology, 61, 989-1006, https://doi.org/10.1111/jpy.70052, 2025. · DOI
- Krause-Jensen, D. and Duarte, C. M.: Substantial role of macroalgae in marine carbon sequestration, Nature Geosci, 9, 737-742, https://doi.org/10.1038/ngeo2790, 2016. · DOI
- Kültz, D. and Gilmour, K. M.: Iono-and Osmoregulation, in: The Physiology of Fishes, CRC Press, 2020.
- Lamb, W. F., Gasser, T., Roman-Cuesta, R. M., Grassi, G., Gidden, M. J., Powis, C. M., Geden, O., Nemet, G., Pratama, Y., Riahi, K., Smith, S. M., Steinhauser, J., Vaughan, N. E., Smith, H. B., and Minx, J. C.: The carbon dioxide removal gap, Nat. Clim. Chang., 14, 644-651, https://doi.org/10.1038/s41558-024-01984-6, 2024. · DOI
- Laurent, P., Wilkie, M. P., Chevalier, C., and Wood, C. M.: The effect of highly alkaline water (pH 9.5) on the morphology and morphometry of chloride cells and pavement cells in the gills of the freshwater rainbow trout: relationship to ionic transport and ammonia excretion, Can. J. Zool., 78, 307-319, https://doi.org/10.1139/z99-207, 2000. · DOI
- Lee, C.-H., Lee, K., Kim, M., Kim, J.-H., Zhang, Y., Kang, J. W., Choi, I. H., Oh, J. C., Choi, Y., Kim, J. H., Kim, J.-M., and Kim, K. Y.: Alkalinity (bicarbonate) pumping by coastal macroalgal forests, Geophysical Research Letters, 52, e2025GL115753, https://doi.org/10.1029/2025GL115753, 2025. · DOI
- Lewis-Smith, C., Norman, K., Root, L., Crim, R., Roberts, S., and Gavery, M.: Navigating ocean acidification in shellfish aquaculture: Stakeholder perspectives of developing strategies in the U.S. Pacific Region, Aquaculture Reports, 42, 102858, https://doi.org/10.1016/j.aqrep.2025.102858, 2025. · DOI
- Liu, Y., Li, L., Zheng, L., Fu, P., Wang, Y., Nguyen, H., Shen, X., and Sui, Y.: Antioxidant responses of triangle sail mussel Hyriopsis cumingii exposed to harmful algae Microcystis aeruginosa and high pH, Chemosphere, 243, 125241, https://doi.org/10.1016/j.chemosphere.2019.125241, 2020. · DOI
- Locke, A., Doe, K. G., Fairchild, W. L., Jackman, P. M., and Reese, E. J.: Preliminary evaluation of effects of invasive tunicate management with acetic acid and calcium hydroxide on non-target marine organisms in Prince Edward Island, Canada, AI, 4, 221-236, https://doi.org/10.3391/ai.2009.4.1.23, 2009. · DOI
- Mackenzie, C. L., Pearce, C. M., Leduc, S., Roth, D., Kellogg, C. T. E., Clemente-Carvalho, R. B. G., and Green, T. J.: Impacts of Seawater pH Buffering on the Larval Microbiome and Carry-Over Effects on Later-Life Disease Susceptibility in Pacific Oysters, Applied and Environmental Microbiology, 88, e01654-22, https://doi.org/10.1128/aem.01654-22, 2022. · DOI
- Maoxiao, P., Bo, Y., Xiaojun, L., Donghong, N., Tianyi, L., Zhiguo, D., and Jiale, L.: Effects of Alkalinity and pH on Survival, Growth, and Enzyme Activities in Juveniles of the Razor Clam, Sinonovacula constricta , Front. Physiol., 9, 552, https://doi.org/10.3389/fphys.2018.00552, 2018. · DOI
- Marín-Samper, L., Arístegui, J., Hernández-Hernández, N., Ortiz, J., Archer, S. D., Ludwig, A., and Riebesell, U.: Assessing the impact of CO 2 -equilibrated ocean alkalinity enhancement on microbial metabolic rates in an oligotrophic system, Biogeosciences, 21, 2859-2876, https://doi.org/10.5194/bg-21-2859-2024, 2024. · DOI
- Martin, P., Van Der Loeff, M. R., Cassar, N., Vandromme, P., d'Ovidio, F., Stemmann, L., Rengarajan, R., Soares, M., González, H. E., Ebersbach, F., Lampitt, R. S., Sanders, R., Barnett, B. A., Smetacek, V., and Naqvi, S. W. A.: Iron fertilization enhanced net community production but not downward particle flux during the Southern Ocean iron fertilization experiment LOHAFEX, Global Biogeochemical Cycles, 27, 871-881, https://doi.org/10.1002/gbc.20077, 2013. · DOI
- Martins Medeiros, I. P. and Souza, M. M.: Acid times in physiology: A systematic review of the effects of ocean acidification on calcifying invertebrates, Environmental Research, 231, 116019, https://doi.org/10.1016/j.envres.2023.116019, 2023. · DOI
- McElhany, P. and Shallin Busch, D.: Appropriate pCO 2 treatments in ocean acidification experiments, Mar Biol, 160, 1807-1812, https://doi.org/10.1007/s00227-012-2052-0, 2013. · DOI
- McElhany, P., Shallin, B., Maher, M., Perez, D., and Rovinski, K.: Population and maternal variation in the sensitivity of Dungeness crab zoea ( Metacracinus magister ) to elevated CO 2 ., Marine Ecology Progress Series, https://doi.org/DOI:%20https://doi.org/10.3354/meps14854, 2025. · DOI
- McKellar, L., McQuatters-Gollop, A., Chaigneau, T., Vina-Herbon, C., Valanko, S., and Hiddink, J. G.: Evaluating methods for setting thresholds for good status in marine ecosystems, ICES Journal of Marine Science, 82, https://doi.org/10.1093/icesjms/fsaf019, 2025. · DOI
- Menéndez, M., Martı ńez, M., and Comı ń, F. A.: A comparative study of the effect of pH and inorganic carbon resources on the photosynthesis of three floating macroalgae species of a Mediterranean coastal lagoon, Journal of Experimental Marine Biology and Ecology, 256, 123-136, https://doi.org/10.1016/S0022-0981(00)00313-0, 2001a. · DOI
- Menéndez, M., Martı ńez, M., and Comı ń, F. A.: A comparative study of the effect of pH and inorganic carbon resources on the photosynthesis of three floating macroalgae species of a Mediterranean coastal lagoon, Journal of Experimental Marine Biology and Ecology, 256, 123-136, https://doi.org/10.1016/S0022-0981(00)00313-0, 2001b. · DOI
- Middelboe, A. L. and Hansen, P. J.: High pH in shallow-water macroalgal habitats, Marine Ecology Progress Series, 338, 107-117, https://doi.org/10.3354/meps338107, 2007. · DOI
- Moras, C. A., Bach, L. T., Cyronak, T., Joannes-Boyau, R., and Schulz, K. G.: Ocean alkalinity enhancement -avoiding runaway CaCO 3 precipitation during quick and hydrated lime dissolution, Biogeosciences, 19, 3537-3557, https://doi.org/10.5194/bg-19-3537-2022, 2022. · DOI
- Moras, C. A., Cyronak, T., Bach, L. T., Joannes-Boyau, R., and Schulz, K. G.: Effects of grain size and seawater salinity on magnesium hydroxide dissolution and secondary calcium carbonate precipitation kinetics: implications for ocean alkalinity enhancement, Biogeosciences, 21, 3463-3475, https://doi.org/10.5194/bg-21-3463-2024, 2024. · DOI
- van de Mortel, H., Bednaršek, N., Pelletier, G., Feely, R. A., Müller, J. D., and Gruber, N.: Substantial limitations of ocean alkalinity enhancement in mitigating the negative impacts of ocean acidification on marine calcifiers, Environ. Sci. Technol., 60, 622-641, https://doi.org/10.1021/acs.est.5c09298, 2026. · DOI
- Mos, B., Byrne, M., and Dworjanyn, S. A.: Effects of low and high pH on sea urchin settlement, implications for the use of alkali to counter the impacts of acidification, Aquaculture, 528, 735618, https://doi.org/10.1016/j.aquaculture.2020.735618, 2020. · DOI
- NASEM: A Research Strategy for Ocean-based Carbon Dioxide Removal and Sequestration, National Academies Press, Washington, D.C., https://doi.org/10.17226/26278, 2022. · DOI
- Ninokawa, A. T., Saley, A. M., Shalchi, R., and Gaylord, B.: Multiple carbonate system parameters independently govern shell formation in a marine mussel, Commun Earth Environ, 5, 273, https://doi.org/10.1038/s43247-024-01440-5, 2024. · DOI
- Nocera, A. C., Traboni, C., Courboulès, J., Romano, F., Chantzaras, C., Magiopoulos, I., Varliero, S., Azzellino, A., Bazzicalupo, P., Macchi, P., Raos, G., Basso, D., and Pitta, P.: The effect of ocean alkalinity https://doi.org/10.5194/egusphere-2026-1597 Preprint. Discussion started: 26 March 2026 c Author(s) 2026. CC BY 4.0 License. enhancement on zooplankton standing stock and community composition in the Eastern Mediterranean Sea: a mesocosm study, Marine Environmental Research, 107489, https://doi.org/10.1016/j.marenvres.2025.107489, 2025. · DOI
- Pajusalu, L., Martin, G., Paalme, T., and Põllumäe, A.: The effect of CO 2 enrichment on net photosynthesis of the red alga Furcellaria lumbricalis in a brackish water environment, PeerJ, 4, e2505, https://doi.org/10.7717/peerj.2505, 2016. · DOI
- Pan, L. and Jiang, L.: The effect of sudden changes in salinity and pH on the immune activity of two species of shrimps, Journal of Ocean University of Qingdao, 32, 903-910, 2002.
- Parra, G. and Yúfera, M.: Tolerance response to water pH in larvae of two marine fish species, gilthead seabream, Sparus aurata (L.) and Senegal sole, Solea senegalensis (Kaup), during development: Tolerance to water pH in fish larvae, Aquaculture Research, 33, 747-752, https://doi.org/10.1046/j.1365-2109.2002.00713.x, 2002. · DOI
- Paul, A. J., Haunost, M., Goldenberg, S. U., Hartmann, J., Sánchez, N., Schneider, J., Suitner, N., and Riebesell, U.: Ocean alkalinity enhancement in an open-ocean ecosystem: biogeochemical responses and carbon storage durability, Biogeosciences, 22, 2749-2766, https://doi.org/10.5194/bg-22-2749-2025, 2025. · DOI
- Quéguiner, B.: Iron fertilization and the structure of planktonic communities in high nutrient regions of the Southern Ocean, Deep Sea Research Part II: Topical Studies in Oceanography, 90, 43-54, https://doi.org/10.1016/j.dsr2.2012.07.024, 2013. · DOI
- Raven, J. A., Giordano, M., Beardall, J., and Maberly, S. C.: Algal evolution in relation to atmospheric CO 2 : carboxylases, carbon-concentrating mechanisms and carbon oxidation cycles, Philos Trans R Soc Lond B Biol Sci, 367, 493-507, https://doi.org/10.1098/rstb.2011.0212, 2012. · DOI
- Reinfelder, J. R.: Carbon concentrating mechanisms in eukaryotic marine phytoplankton, Annual Review of Marine Science, 3, 291-315, https://doi.org/10.1146/annurev-marine-120709-142720, 2011. · DOI
- Renforth, P. and Henderson, G.: Assessing ocean alkalinity for carbon sequestration, Reviews of Geophysics, 55, 636-674, https://doi.org/10.1002/2016RG000533, 2017. · DOI
- Ricart, A. M., Ward, M., Hill, T. M., Sanford, E., Kroeker, K. J., Takeshita, Y., Merolla, S., Shukla, P., Ninokawa, A. T., Elsmore, K., and Gaylord, B.: Coast-wide evidence of low pH amelioration by seagrass ecosystems, Global Change Biology, 27, 2580-2591, https://doi.org/10.1111/gcb.15594, 2021a. · DOI
- Ricart, A. M., Gaylord, B., Hill, T. M., Sigwart, J. D., Shukla, P., Ward, M., Ninokawa, A., and Sanford, E.: Seagrass-driven changes in carbonate chemistry enhance oyster shell growth, Oecologia, 196, 565-576, https://doi.org/10.1007/s00442-021-04949-0, 2021b. · DOI
- Riebesell, U., Fabry, V. J., Hansson, L., and Gattuso, J.-P.: Guide to best practices for ocean acidification research and data reporting, edited by: Riebesell, U., Fabry, V. J., Hansson, L., and Gattuso, J.-P., Office for Official Publications of the European Communities, Luxembourg, 258 pp., https://doi.org/10.2777/66906, 2011. · DOI
- Ries, J. B., Cohen, A. L., and McCorkle, D. C.: Marine calcifiers exhibit mixed responses to CO 2 -induced ocean acidification, Geology, 37, 1131-1134, https://doi.org/10.1130/G30210A.1, 2009. · DOI
- Ringham, M. C., Hirtle, N., Shaw, C., Lu, X., Herndon, J., Carter, B. R., and Eisaman, M. D.: An assessment of ocean alkalinity enhancement using aqueous hydroxides: kinetics, efficiency, and precipitation thresholds, Biogeosciences, 21, 3551-3570, https://doi.org/10.5194/bg-21-3551-2024, 2024. · DOI
- Robinson, J., Popova, E. E., Srokosz, M. A., and Yool, A.: A tale of three islands: Downstream natural iron fertilization in the Southern Ocean, JGR Oceans, 121, 3350-3371, https://doi.org/10.1002/2015JC011319, 2016. · DOI
- Ross, P. M., Parker, L., O'Connor, W. A., and Bailey, E. A.: The impact of ocean acidification on reproduction, early development and settlement of marine organisms, Water, 3, 1005-1030, https://doi.org/10.3390/w3041005, 2011. · DOI
- Rounds, S. A. and Wilde, F. D.: Chapter A6. Section 6.6. Alkalinity and acid neutralizing capacity (Version 3, Revised Jul 2006): U.S. Geological Survey Techniques of Water-Resources Investigations 09-A6.6, USGS, 2012.
- Schlüter, L., Lohbeck, K. T., Gutowska, M. A., Gröger, J. P., Riebesell, U., and Reusch, T. B. H.: Adaptation of a globally important coccolithophore to ocean warming and acidification, Nature Clim Change, 4, 1024-1030, https://doi.org/10.1038/nclimate2379, 2014. · DOI
- Scott, D. M. and Wilson, R. W.: Three species of fishes from an eutrophic, seasonally alkaline lake are not more tolerant to acute exposure to high pH in the laboratory, Journal of Fish Biology, 70, 551-566, https://doi.org/10.1111/j.1095-8649.2007.01329.x, 2007. · DOI
- Scott, D. M., Lucas, M. C., and Wilson, R. W.: The effect of high pH on ion balance, nitrogen excretion and behaviour in freshwater fish from an eutrophic lake: A laboratory and field study, Aquatic Toxicology, 73, 31-43, https://doi.org/10.1016/j.aquatox.2004.12.013, 2005. · DOI
- Sensui, N., Itoh, Y., Okura, N., Shiba, K., Baba, S. A., Inaba, K., and Yoshida, M.: Spawning-induced pH increase activates sperm attraction and fertilization abilities in eggs of the ascidian, Phallusia philippinensis and Ciona intestinalis , Int J Mol Sci, 24, 2666, https://doi.org/10.3390/ijms24032666, 2023. · DOI
- Shumway, S. E., Card, D., Getchell, R., and Newell, C.: Effects of calcium oxide (quicklime) on non-target organisms in mussel beds, Bull. Environ. Contam. Toxicol., 40, 503-509, https://doi.org/10.1007/BF01688373, 1988a. · DOI
- Shumway, S. E., Card, D., Getchell, R., and Newell, C.: Effects of calcium oxide (quicklime) on non-target organisms in mussel beds, Bull. Environ. Contam. Toxicol., 40, 503-509, https://doi.org/10.1007/BF01688373, 1988b. https://doi.org/10.5194/egusphere-2026-1597 Preprint. Discussion started: 26 March 2026 c Author(s) 2026. CC BY 4.0 License. State of California: Water Quality Control Policy for Developing California's Clean Water Act Section 303(d) List, State Water Resources Control Board, 2004. State of Oregon: Methodology for Oregon's 2012 Water Quality Report and List of Water Quality Limited Waters (Pursuant to Clean Water Act Sections 303(d) and 305(b) and OAR 340-041-0046), 2014. State of Washington: Assessment policy 1-11 -Washington State Department of Ecology, Department of Ecology, 2012. · DOI
- Strand, H. K., Christie, H., Fagerli, C. W., Mengede, M., and Moy, F.: Optimizing the use of quicklime (CaO) for sea urchin management -A lab and field study, Ecological Engineering, 143, 100018, https://doi.org/10.1016/j.ecoena.2020.100018, 2020. · DOI
- Subhas, A. V., Marx, L., Reynolds, S., Flohr, A., Mawji, E. W., Brown, P. J., and Cael, B. B.: Microbial ecosystem responses to alkalinity enhancement in the North Atlantic Subtropical Gyre, Front. Clim., 4, https://doi.org/10.3389/fclim.2022.784997, 2022. · DOI
- Subhas, A. V., Lehmann, N., and Rickaby, R. E. M.: Natural analogs to ocean alkalinity enhancement, State of the Planet, 2-oae2023, 8, https://doi.org/10.5194/sp-2-oae2023-8-2023, 2023. · DOI
- Suitner, N., Faucher, G., Lim, C., Schneider, J., Moras, C. A., Riebesell, U., and Hartmann, J.: Ocean alkalinity enhancement approaches and the predictability of runaway precipitation processes: results of an experimental study to determine critical alkalinity ranges for safe and sustainable application scenarios, Biogeosciences, 21, 4587-4604, https://doi.org/10.5194/bg-21-4587-2024, 2024a. · DOI
- Suitner, N., Faucher, G., Lim, C., Schneider, J., Moras, C. A., Riebesell, U., and Hartmann, J.: Ocean alkalinity enhancement approaches and the predictability of runaway precipitation processes: results of an experimental study to determine critical alkalinity ranges for safe and sustainable application scenarios, Biogeosciences, 21, 4587-4604, https://doi.org/10.5194/bg-21-4587-2024, 2024b. · DOI
- Sun, J., Zhao, C., Zhao, S., Dai, W., Liu, J., Zhang, J., Xu, J., and He, P.: Diversity of CO 2 Concentrating Mechanisms in Macroalgae Photosynthesis: A Case Study of Ulva sp., Journal of Marine Science and Engineering, 11, https://doi.org/10.3390/jmse11101911, 2023. · DOI
- Sunday, J. M., Calosi, P., Dupont, S., Munday, P. L., Stillman, J. H., and Reusch, T. B. H.: Evolution in an acidifying ocean, Trends in Ecology & Evolution, 29, 117-125, https://doi.org/http://dx.doi.org/10.1016/j.tree.2013.11.001, 2014. · DOI
- Sundin, J.: The effects of ocean acidification on fishes -history and future outlook, https://doi.org/10.1111/jfb.15323, 2022. · DOI
- Taraldsvik, M. and Myklestad, S. M.: The effect of pH on growth rate, biochemical composition and extracellular carbohydrate production of the marine diatom Skeletonema costatum , European Journal of Phycology, 35, 189-194, https://doi.org/10.1080/09670260010001735781, 2000. · DOI
- Thiele, S., Fuchs, B. M., Ramaiah, N., and Amann, R.: Microbial community response during the iron fertilization experiment LOHAFEX, Appl Environ Microbiol, 78, 8803-8812, https://doi.org/10.1128/AEM.01814-12, 2012. https://doi.org/10.5194/egusphere-2026-1597 Preprint. Discussion started: 26 March 2026 c Author(s) 2026. CC BY 4.0 License. · DOI
- Tinoco, A. I., Mitchison-Field, L. M. Y., Bradford, J., Renicke, C., Perrin, D., Bay, L. K., Pringle, J. R., and Cleves, P. A.: Role of the bicarbonate transporter SLC4γ in stony-coral skeleton formation and evolution, Proceedings of the National Academy of Sciences, 120, e2216144120, https://doi.org/10.1073/pnas.2216144120, 2023. · DOI
- Torres, O., Kwiatkowski, L., Sutton, A. J., Dorey, N., and Orr, J. C.: Characterizing mean and extreme diurnal variability of ocean CO 2 system variables across marine environments, Geophysical Research Letters, 48, e2020GL090228, https://doi.org/10.1029/2020GL090228, 2021. · DOI
- Trick, C. G., Bill, B. D., Cochlan, W. P., Wells, M. L., Trainer, V. L., and Pickell, L. D.: Iron enrichment stimulates toxic diatom production in high-nitrate, low-chlorophyll areas, Proceedings of the National Academy of Sciences, 107, 5887-5892, https://doi.org/10.1073/pnas.0910579107, 2010. USEPA: Quality Criteria for Water (Red Book), U.S. Environmental Protection Agency, Washington, DC, 1976. USEPA: Series 850 -Ecological Effects Test Guidelines, 2015. · DOI
- Van Dam, B., Lopes, C., Zeller, M. A., Ribas-Ribas, M., Wang, H., and Thomas, H.: Overstated potential for seagrass meadows to mitigate coastal ocean acidification, Front. Mar. Sci., 8, https://doi.org/10.3389/fmars.2021.729992, 2021. · DOI
- Van Oijen, T., Veldhuis, M. J. W., Gorbunov, M. Y., Nishioka, J., Van Leeuwe, M. A., and De Baar, H. J. W.: Enhanced carbohydrate production by Southern Ocean phytoplankton in response to in situ iron fertilization, Marine Chemistry, 93, 33-52, https://doi.org/10.1016/j.marchem.2004.06.039, 2005. · DOI
- Vandelannoote, R., Van't Dack, L., and Van Grieken, R.: Effects of alkaline aluminate waste dumping on seawater chemistry, Marine Environmental Research, 21, 275-288, https://doi.org/10.1016/0141-1136(87)90050-X, 1987. · DOI
- Viechtbauer, W.: Conducting Meta-Analyses in R with the metafor Package, Journal of Statistical Software, 36, 1-48, https://doi.org/10.18637/jss.v036.i03, 2010. · DOI
- Wagner, E. J., Bosakowski, T., and Intelmann, S.: Combined effects of temperature and high pH on mortality and the stress response of rainbow trout after stocking, Transactions of the American Fisheries Society, 126, 985-998, https://doi.org/10.1577/1548-8659(1997)126%3C0985:CEOTAH%3E2.3.CO;2, 1997. · DOI
- Wang, W.-N., Wang, A.-L., Chen, L., Liu, Y., and Sun, R.-Y.: Effects of pH on survival, phosphorus concentration, adenylate energy charge and Na+-K+ ATPase activities of Penaeus chinensis Osbeck juveniles, Aquatic Toxicology, 60, 75-83, https://doi.org/10.1016/S0166-445X(01)00271-5, 2002. · DOI
- Watson, S. C. L., Somerfield, P. J., Lemasson, A. J., Knights, A. M., Edwards-Jones, A., Nunes, J., Pascoe, C., McNeill, C. L., Schratzberger, M., Thompson, M. S. A., Couce, E., Szostek, C. L., Baxter, H., and Beaumont, N. J.: The global impact of offshore wind farms on ecosystem services, Ocean & Coastal Management, 249, 107023, https://doi.org/10.1016/j.ocecoaman.2024.107023, 2024. https://doi.org/10.5194/egusphere-2026-1597 Preprint. Discussion started: 26 March 2026 c Author(s) 2026. CC BY 4.0 License. · DOI
- Weisberg, S. B., Bednaršek, N., Feely, R. A., Chan, F., Boehm, A. B., Sutula, M., Ruesink, J. L., Hales, B., Largier, J. L., and Newton, J. A.: Water quality criteria for an acidifying ocean: Challenges and opportunities for improvement, Ocean & Coastal Management, 126, 31-41, https://doi.org/10.1016/j.ocecoaman.2016.03.010, 2016. · DOI
- Wilkie, M. P. and Wood, C. M.: Nitrogenous waste excretion, acid-base regulation, and ionoregulation in rainbow trout ( Oncorhynchus mykiss ) exposed to extremely alkaline water, Physiological Zoology, 64, 1069-1086, https://doi.org/10.1086/physzool.64.4.30157957, 1991. · DOI
- Wilkie, M. P. and Wood, C. M.: The effects of extremely alkaline water (pH 9•5) on rainbow trout gill function and morphology, Journal of Fish Biology, 45, 87-98, https://doi.org/10.1111/j.1095-8649.1994.tb01288.x, 1994. · DOI
- Wilkie, M. P. and Wood, C. M.: Recovery from high pH exposure in the rainbow trout: white muscle ammonia storage, ammonia washout, and the restoration of blood chemistry, Physiological Zoology, 68, 379-401, https://doi.org/10.1086/physzool.68.3.30163775, 1995. · DOI
- Witschi, W. A. and Ziebell, C. D.: Evaluation of pH shock on hatchery-reared rainbow trout, The Progressive Fish-Culturist, 41, 3-5, https://doi.org/10.1577/1548-8659(1979)41%5B3:EOPSOH%5D2.0.CO;2, 1979. · DOI
- Wu, Z., Cai, C., Ye, Z., Wang, N., Zhu, Y., Jin, R., Christakos, G., Chen, S., Wang, D., Zhu, J., He, J., Agusti, S., Duarte, C. M., and Wu, J.: Macroalgae farming increases DO and pH, reduces pCO 2 and nutrients, and enhances blue carbon potential, Earth Syst Environ, https://doi.org/10.1007/s41748-025-00867-w, 2025. · DOI
- Xiong, T., Li, H., Yue, Y., Hu, Y., Zhai, W., Xue, L., Jiao, N., and Zhang, Y.: Legacy effects of late macroalgal blooms on dissolved inorganic carbon pool through alkalinity enhancement in coastal ocean, Environ. Sci. Technol., 57, 2186-2196, https://doi.org/10.1021/acs.est.2c09261, 2023. · DOI
- Xue, S., Mao, Y., Wang, J., Fang, J., and Zhao, F.: Effects of salinity, carbonate alkalinity, and pH on physiological indicators of nutrition transporter for potential habitat restoration of amphipod Eogammarus possjeticus , J. Ocean. Limnol., 38, 1925-1935, https://doi.org/10.1007/s00343-020-0063-0, 2020. · DOI
- Yang, Y., Brockmann, P., Galdino, C., Schindler, U., and Gazeau, F.: An update of data compilation on the biological response to ocean acidification and overview of the OA-ICC data portal, Earth System Science Data, 16, 3771-3780, https://doi.org/10.5194/essd-16-3771-2024, 2024. · DOI
- Yao, Z., Wang, H., Zhou, K., Ying, C., and Lai, Q.: Effects of water carbonate alkalinity and pH on survival rate of post-larval Litopenaeus vannamei , Chinese Journal of Ecology, 29, 945-950, 2010a.
- Yao, Z. L., Lai, Q. F., Zhou, K., Rizalita, R.-E., and Wang, H.: Developmental biology of medaka fish ( Oryzias latipes ) exposed to alkalinity stress, Journal of Applied Ichthyology, 26, 397-402, https://doi.org/10.1111/j.1439-0426.2009.01360.x, 2010b. · DOI
- Yoon, J.-E., Yoo, K.-C., Macdonald, A. M., Yoon, H. I., Park, K.-T., Yang, E.-J., Kim, H.-C., Lee, J. I., Lee, M. K., Jung, J., Park, J., Song, J.-M., Choi, T.-J., Kim, K., and Kim, I.-N.: Ocean iron fertilization https://doi.org/10.5194/egusphere-2026-1597 Preprint. Discussion started: 26 March 2026 c Author(s) 2026. CC BY 4.0 License. experiments: past-present-future with introduction to Korean Iron Fertilization Experiment in the Southern Ocean (KIFES) project, https://doi.org/10.5194/bg-2016-472, 15 November 2016. · DOI
- Young, C. S., Sylvers, L. H., Tomasetti, S. J., Lundstrom, A., Schenone, C., Doall, M. H., and Gobler, C. J.: Kelp ( Saccharina latissima ) mitigates coastal ocean acidification and increases the growth of North Atlantic bivalves in lab experiments and on an oyster farm, Front. Mar. Sci., 9, https://doi.org/10.3389/fmars.2022.881254, 2022. · DOI
- Zhang, L., Pan, L., and Luan, Z.: Effects of pH on ion-transport enzyme activities and survival, growth of Marsupenaeus japonicus postlarvae, Journal of Fisheries of China, 32, 758-765, 2008.
- Zhang, Y., Bach, L. T., Lohbeck, K. T., Schulz, K. G., Listmann, L., Klapper, R., and Riebesell, U.: Population-specific responses in physiological rates of Emiliania huxleyi to a broad CO 2 range, Biogeosciences, 15, 3691-3701, https://doi.org/10.5194/bg-15-3691-2018, 2018. 68 1721 1722 1723 1724 1725 1726 1727 1728 1729 1730 1731 https://doi.org/10.5194/egusphere-2026-1597 Preprint. Discussion started: 26 March 2026 c Author(s) 2026. CC BY 4.0 License. · DOI
Cited by
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Grabb, K. C., Wood, M., & McElhany, P. (2026) · doi:10.70212/cdrxiv.2026519.v1 · Cited by 2 · see citing works
Self-citationGrabb, K. C., Kitch, G. D., Findlay, H. S., Gurney‐Smith, H., Myridinas, M., McElhany, P., Hogan, F., Cape, M., Sánchez, N., Stiasny, M., et al. (2026) · ICES Journal of Marine Science · doi:10.1093/icesjms/fsag076 · Cited by 1 · see citing works
Self-citationBiogeochemical responses to ocean alkalinity enhancement in the North China Sea
Xin, X., Liu, Y., Chang, R., Lei, R., Zhu, M., Wang, X., Wang, X. C., & Liu, J. (2026) · EGUsphere · doi:10.5194/egusphere-2026-5281
Stability assessment of calcium carbonate dissolution as a marine carbon dioxide removal mechanism
Melendez-Perez, A. B., Gilbert, K., & Cyronak, T. J. (2026) · Frontiers in Marine Science · doi:10.3389/fmars.2026.1796693
Marine Carbonate System Observing and mCDR: New Processes, Needs, and Systems
Cross, J., Achterberg, E. P., Atamanchuk, D., Bresnahan, P. J., Byrne, R. H., DeGrandpre, M. D., Fennel, K., Hales, B., Loucaides, S., Martz, T. R., et al. (2026) · Chemical Reviews · doi:10.1021/acs.chemrev.5c01007
- Authors
- McElhany, P., Cape, M., Faucher, G., Frieder, C., Hemery, L. G., Iglesias-Rodriguez, D., Murray, C. S., & Noble, W.
- Affiliations
- NOAA National Marine Fisheries Service Northwest Fisheries Science Center (US)
- Environmental Defense Fund (US)
- GEOMAR Helmholtz Centre for Ocean Research Kiel (DE)
- Southern California Coastal Water Research Project (US)
- Pacific Northwest National Laboratory (US)
- Woods Hole Oceanographic Institution (US)
- University of California, Santa Barbara (US)
- Corresponding author
- McElhany, Paul
- ORCID
- Publisher
- Copernicus GmbH
- Published
- 2026-03-26
- OpenAlex
- W7140558308
- Cited by
- 3
- References
- 0
- Citations by year
- 2026: 3
- Type
- posted content
- Language
- en
- Open access
- green
- doi.org
- Licence
- Locations
- Helmholtz Centre for Ocean Research Kiel (GEOMAR) (submittedVersion, cc-by)
- Funders
- Northwest Fisheries Science Center (na)
- Ocean Acidification Program (na)
- Topics
- Physical Sciences › Earth and Planetary Sciences › Oceanography › Ocean Acidification Effects and Responses
- Physical Sciences › Environmental Science › Environmental Engineering › CO2 Sequestration and Geologic Interactions
- Physical Sciences › Materials Science › Biomaterials › Calcium Carbonate Crystallization and Inhibition
- Keywords
- marine carbon dioxide removal, carbonate chemistry, biological thresholds, ocean alkalinity, high pH, ocean acidification, marine organisms, physiological responses, threshold estimation, ocean alkalinity enhancement
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