Not logged in
PANGAEA.
Data Publisher for Earth & Environmental Science

Ocean Acidification, International Coordination Centre (2015): Data compilation on the biological response to ocean acidification: environmental and experimental context of data sets and related literature. PANGAEA, https://doi.org/10.1594/PANGAEA.149999, Supplement to: Yang, Yan; Hansson, L; Gattuso, Jean-Pierre (2016): Data compilation on the biological response to ocean acidification: an update. Earth System Science Data, 8(1), 79-87, https://doi.org/10.5194/essd-8-79-2016

Always quote above citation when using data! You can download the citation in several formats below.

RIS CitationBibTeX Citation

Abstract:
The exponential growth of studies on the biological response to ocean acidification over the last few decades has generated a large amount of data. To facilitate data comparison, a data compilation hosted at the data publisher PANGAEA was initiated in 2008 and is updated on a regular basis (doi:10.1594/PANGAEA.149999). By January 2015, a total of 581 data sets (over 4 000 000 data points) from 539 papers had been archived. Here we present the developments of this data compilation five years since its first description by Nisumaa et al. (2010). Most of study sites from which data archived are still in the Northern Hemisphere and the number of archived data from studies from the Southern Hemisphere and polar oceans are still relatively low. Data from 60 studies that investigated the response of a mix of organisms or natural communities were all added after 2010, indicating a welcomed shift from the study of individual organisms to communities and ecosystems. The initial imbalance of considerably more data archived on calcification and primary production than on other processes has improved. There is also a clear tendency towards more data archived from multifactorial studies after 2010. For easier and more effective access to ocean acidification data, the ocean acidification community is strongly encouraged to contribute to the data archiving effort, and help develop standard vocabularies describing the variables and define best practices for archiving ocean acidification data.
Related to:
Aberle, Nicole; Schulz, Kai Georg; Stuhr, Annegret; Malzahn, Arne M; Ludwig, Andrea; Riebesell, Ulf (2013): High tolerance of microzooplankton to ocean acidification in an Arctic coastal plankton community. Biogeosciences, 10(3), 1471-1481, https://doi.org/10.5194/bg-10-1471-2013
Agostini, Sylvain; Fujimura, Hiroyuki; Higuchi, Tomihiko; Yuyama, Ikuko; Casareto, Beatriz E; Suzuki, Yoshimi; Nakano, Yoshiyuki (2013): The effects of thermal and high-CO2 stresses on the metabolism and surrounding microenvironment of the coral Galaxea fascicularis. Comptes Rendus Biologies, 336(8), 384-391, https://doi.org/10.1016/j.crvi.2013.07.003
Albright, R; Mason, B; Langdon, Chris (2008): Effect of aragonite saturation state on settlement and post-settlement growth of Porites astreoides larvae. Coral Reefs, 27(3), 485-490, https://doi.org/10.1007/s00338-008-0392-5
Alexandre, Ana; Silva, João; Buapet, Pimchanok; Björk, Mats; Santos, Rui (2012): Effects of CO2 enrichment on photosynthesis, growth, and nitrogen metabolism of the seagrass Zostera noltii. Ecology and Evolution, 2(10), 2625-2635, https://doi.org/10.1002/ece3.333
Allan, Bridie J M; Domenici, Paolo; McCormick, Mark I; Watson, Sue-Ann; Munday, Philip L (2013): Elevated CO2 Affects Predator-Prey Interactions through Altered Performance. PLoS ONE, 8(3), e58520, https://doi.org/10.1371/journal.pone.0058520.t002
Allan, Bridie J M; Miller, Garielle M; McCormick, Mark I; Domenici, Paolo; Munday, Philip L (2014): Parental effects improve escape performance of juvenile reef fish in a high-CO2 world. Proceedings of the Royal Society B-Biological Sciences, 281(1777), 20132179-20132179, https://doi.org/10.1098/rspb.2013.2179
Allen, Katherine A; Hönish, Bärbel; Eggins, Stephen M; Yu, Jimin; Spero, Howard J; Elderfield, Henry (2011): Controls on boron incorporation in cultured tests of the planktic foraminifer Orbulina universa. Earth and Planetary Science Letters, 309(3-4), 291-301, https://doi.org/10.1016/j.epsl.2011.07.010
Allgaier, Martin; Riebesell, Ulf; Vogt, Meike; Thyrhaug, Runar; Grossart, Hans-Peter (2008): Coupling of heterotrophic bacteria to phytoplankton bloom development at different pCO2 levels: a mesocosm study. Biogeosciences, 5(4), 1007-1022, https://doi.org/10.5194/bg-5-1007-2008
Allison, Nicola; Cohen, Itay; Finch, Adrian A; Erez, Jonathan; EMIF (2011): Controls on Sr/Ca and Mg/Ca in scleractinian corals: The effects of Ca-ATPase and transcellular Ca channels on skeletal chemistry. Geochimica et Cosmochimica Acta, 75(21), 6350-6360, https://doi.org/10.1016/j.gca.2011.08.012
Alsterberg, Christian; Eklöf, Johan S; Gamfeldt, Lars; Havenhand, Jon N; Sundbäck, Kristina (2013): Consumers mediate the effects of experimental ocean acidification and warming on primary producers. Proceedings of the National Academy of Sciences, 110(21), 8603-8608, https://doi.org/10.1073/pnas.1303797110
Andersen, Sissel; Grefsrud, E S; Harboe, T (2013): Effect of increased pCO2 level on early shell development in great scallop (Pecten maximus Lamarck) larvae. Biogeosciences, 10(10), 6161-6184, https://doi.org/10.5194/bg-10-6161-2013
Andersson, Andreas J; Kuffner, Ilsa B; Mackenzie, Fred T; Jokiel, Paul L; Rodgers, Kuulei S; Tan, A (2009): Net Loss of CaCO3 from a subtropical calcifying community due to seawater acidification: mesocosm-scale experimental evidence. Biogeosciences, 6(8), 1811-1823, https://doi.org/10.5194/bg-6-1811-2009
Andersson, Andreas J; Mackenzie, Fred T; Bates, Nicolas R (2008): Life on the margin: implications of ocean acidification on Mg-calcite, high latitude and cold-water marine calcifiers. Marine Ecology Progress Series, 373, 265-273, https://doi.org/10.3354/meps07639
Anlauf, Holger; D'Croz, Luis; O'Dea, Aaron (2011): A corrosive concoction: The combined effects of ocean warming and acidification on the early growth of a stony coral are multiplicative. Journal of Experimental Marine Biology and Ecology, 397(1), 13-20, https://doi.org/10.1016/j.jembe.2010.11.009
Anthony, Kenneth R N; Kline, David I; Diaz-Pulido, Guillermo; Dove, Sophie; Hoegh-Guldberg, Ove (2008): Ocean acidification causes bleaching and productivity loss in coral reef builders. Proceedings of the National Academy of Sciences of the United States of America, 105(45), 7442-7446, https://doi.org/10.1073/pnas.0804478105
Antia, Avan N; Suffrian, K; Holste, Linda; Müller, Marius N; Nejstgaard, Jens; Simonelli, P; Carotenuto, Y; Putzeys, S (2008): Dissolution of coccolithophorid calcite by microzooplankton and copepod grazing. Biogeosciences Discussions, 5(1), 1-23, https://doi.org/10.5194/bgd-5-1-2008
Apostolaki, Eugenia; Vizzini, Salvatrice; Hendriks, Iris; Olsen, Ylva (2014): Seagrass ecosystem response to long-term high CO2 in a Mediterranean volcanic vent. Marine Environmental Research, 99, 9-15, https://doi.org/10.1016/j.marenvres.2014.05.008
Appelhans, Yasmin S; Thomsen, Jörn; Opitz, Stephan; Pansch, Christian; Melzner, Frank; Wahl, Martin (2014): Juvenile sea stars exposed to acidification decrease feeding and growth with no acclimation potential. Marine Ecology Progress Series, 509, 227-239, https://doi.org/10.3354/meps10884
Archer, S D; Kimmance, S A; Stephens, J A; Hopkins, Frances E; Bellerby, Richard G J; Schulz, Kai Georg; Piontek, Judith; Engel, Anja (2013): Contrasting responses of DMS and DMSP to ocean acidification in Arctic waters. Biogeosciences, 10(3), 1893-1908, https://doi.org/10.5194/bg-10-1893-2013
Arnold, Thomas; Freundlich, Grace; Weilnau, Taylor; Verdi, Arielle; Tibbetts, Ian R (2014): Impacts of groundwater discharge at Myora Springs (North Stradbroke Island, Australia) on the phenolic metabolism of eelgrass, Zostera muelleri, and grazing by the juvenile rabbitfish, Siganus fuscescens. PLoS ONE, 9(8), e104738, https://doi.org/10.1371/journal.pone.0104738.t003
Arnold, Thomas; Mealey, Christopher; Leahey, Hannah; Miller, A Whitman; Hall-Spencer, Jason M; Milazzo, Marco; Maers, Kelly (2012): Ocean Acidification and the Loss of Phenolic Substances in Marine Plants. PLoS ONE, 7(4), e35107, https://doi.org/10.1371/journal.pone.0035107.t004
Arnosti, Carol; Grossart, Hans-Peter; Mühling, M; Joint, Ian; Passow, Uta (2011): Dynamics of extracellular enzyme activities in seawater under changed atmospheric pCO2: a mesocosm investigation. Aquatic Microbial Ecology, 64(3), 285-298, https://doi.org/10.3354/ame01522
Asnaghi, Valentina; Chiantore, Mariachiara; Mangialajo, Luisa; Gazeau, Frédéric; Francour, Patrice; Alliouane, Samir; Gattuso, Jean-Pierre (2013): Cascading Effects of Ocean Acidification in a Rocky Subtidal Community. PLoS ONE, 8(4), e61978, https://doi.org/10.1371/journal.pone.0061978.t004
Asnaghi, Valentina; Mangialajo, Luisa; Gattuso, Jean-Pierre; Francour, Patrice; Privitera, Davide; Chiantore, Mariachiara (2014): Effects of ocean acidification and diet on thickness and carbonate elemental composition of the test of juvenile sea urchins. Marine Environmental Research, 93, 78-84, https://doi.org/10.1016/j.marenvres.2013.08.005
Bach, Lennart Thomas; Mackinder, Luke C M; Schulz, Kai Georg; Wheeler, Glen; Schroeder, Declan C; Brownlee, Colin; Riebesell, Ulf (2013): Dissecting the impact of CO2 and pH on the mechanisms of photosynthesis and calcification in the coccolithophore Emiliania huxleyi. New Phytologist, 199(1), 121-134, https://doi.org/10.1111/nph.12225
Bach, Lennart Thomas; Riebesell, Ulf; Schulz, Kai Georg (2011): Distinguishing between the effects of ocean acidification and ocean carbonation in the coccolithophore Emiliania huxleyi. Limnology and Oceanography, 56(6), 2040-2050, https://doi.org/10.4319/lo.2011.56.6.2040
Baggini, Cecilia; Salomidi, Maria; Voutsinas, Emanuela; Bray, Laura; Krasakopoulou, Evangelia; Hall-Spencer, Jason M (2014): Seasonality Affects Macroalgal Community Response to Increases in pCO2. PLoS ONE, 9(9), e106520, https://doi.org/10.1371/journal.pone.0106520
Barcelos e Ramos, Joana; Biswas, Haimanti; Schulz, Kai Georg; LaRoche, Julie; Riebesell, Ulf (2007): Effect of rising atmospheric carbon dioxide on the marine nitrogen fixer Trichodesmium. Global Biogeochemical Cycles, 21, https://doi.org/10.1029/2006GB002898
Barcelos e Ramos, Joana; Müller, Marius N; Riebesell, Ulf (2010): Short-term response of the coccolithophore Emiliania huxleyi to an abrupt change in seawater carbon dioxide concentrations. Biogeosciences, 7(1), 177-186, https://doi.org/10.5194/bg-7-177-2010
Barcelos e Ramos, Joana; Schulz, Kai Georg; Brownlee, Colin; Sett, Scarlett; Azevedo, Eduardo Brito (2014): Effects of Increasing Seawater Carbon Dioxide Concentrations on Chain Formation of the Diatom Asterionellopsis glacialis. PLoS ONE, 9(3), e90749, https://doi.org/10.1371/journal.pone.0090749
Basallote, M Dolores; De Orte, Manoela R; DelValls, T Angel; Riba, Inmaculada (2014): Studying the Effect of CO2-Induced Acidification on Sediment Toxicity Using Acute Amphipod Toxicity Test. Environmental Science & Technology, 48(15), 8864-8872, https://doi.org/10.1021/es5015373
Bates, Nicolas R; Amat, A; Andersson, Andreas J (2010): Feedbacks and responses of coral calcification on the Bermuda reef system to seasonal changes in biological processes and ocean acidification. Biogeosciences, 7(8), 2509-2530, https://doi.org/10.5194/bg-7-2509-2010
Baumann, Hannes; Talmage, Stephanie C; Gobler, Christopher J (2012): Reduced early life growth and survival in a fish in direct response to increased carbon dioxide. Nature Climate Change, 2, 38-41, https://doi.org/10.1038/nclimate1291
Beaufort, Luc; Probert, Ian; de Garidel-Thoron, Thibault; Bendif, E M; Ruiz-Pino, Diana; Metzi, N; Goyet, Catherine; Buchet, Noëlle; Coupel, P; Grelaud, Michaël; Rost, Bjoern; Rickaby, Rosalind E M; De Vargas, Colomban (2011): Sensitivity of coccolithophores to carbonate chemistry and ocean acidification. Nature, 476, 80-83, https://doi.org/10.1038/nature10295
Bechmann, Renée Katrin; Taban, Ingrid Christina; Westerlund, Stig; Godal, Brit Fjone; Arnberg, Maj; Vingen, Sjur; Ingvarsdottir, Anna; Baussant, Thierry (2011): Effects of ocean acidification on early life stages of shrimp (Pandalus borealis) and mussel (Mytilus edulis). Journal of Toxicology and Environmental Health-Part A-Current Issues, 74(7-9), 424-438, https://doi.org/10.1080/15287394.2011.550460
Bednaršek, Nina; Tarling, Geraint A; Bakker, Dorothee C E; Fielding, Sophie; Cohen, Anne L; Kuzirian, Alan; McCorkle, Daniel C; Lézé, Bertrand; Montagna, Roberto (2012): Description and quantification of pteropod shell dissolution: A sensitive bioindicator of ocean acidification. Global Change Biology, 18(7), 2378-2388, https://doi.org/10.1111/j.1365-2486.2012.02668.x
Bednaršek, Nina; Tarling, Geraint A; Bakker, Dorothee C E; Fielding, Sophie; Jones, Elizabeth M; Venables, H J; Ward, Peter; Kuzirian, Alan; Lézé, Bertrand; Feely, Richard A; Murphy, Eugene J (2012): Extensive dissolution of live pteropods in the Southern Ocean. Nature Geoscience, 5(12), 881-885, https://doi.org/10.1038/ngeo1635
Bellerby, Richard G J; Schulz, Kai Georg; Riebesell, Ulf; Neill, Craig; Nondal, G; Heegaard, E; Johannessen, Truls; Brown, K R (2008): Marine ecosystem community carbon and nutrient uptake stoichiometry under varying ocean acidification during the PeECE III experiment. Biogeosciences, 5(6), 1517-1527, https://doi.org/10.5194/bg-5-1517-2008
Beniash, Elia; Ivanina, Anna; Lieb, Nicholas S; Kurochkin, Ilya; Sokolova, Inna A (2010): Elevated level of carbon dioxide affects metabolism and shell formation in oysters Crassostrea virginica. Marine Ecology Progress Series, 419, 95-108, https://doi.org/10.3354/meps08841
Bibby, Ruth; Cleall-Harding, Polly; Rundle, Simon; Widdicombe, Stephen; Spicer, John I (2007): Ocean acidification disrupts induced defences in the intertidal gastropod Littorina littorea. Biology Letters, 3(6), 699-701, https://doi.org/10.1098/rsbl.2007.0457
Bibby, Ruth; Widdicombe, Stephen; Parry, Helen E; Spicer, John I; Pipe, R (2008): Effects of ocean acidification on the immune response of the blue mussel Mytilus edulis. Aquatic Biology, 2(1), 97-74, https://doi.org/10.3354/ab00037
Biermann, Antje; Engel, Anja (2010): Effect of CO2 on the properties and sinking velocity of aggregates of the coccolithophore Emiliania huxleyi. Biogeosciences, 7(3), 1017-1029, https://doi.org/10.5194/bg-7-1017-2010
Biswas, Haimanti; Cros, Alexander; Yadav, Kamana; Ramana, V Venkata; Prasad, V Rajendra; Archaryya, Tamoghna; Babu, P V Raghunadh (2011): The response of a natural phytoplankton community from the Godavari River Estuary to increasing CO2 concentration during the pre-monsoon period. Journal of Experimental Marine Biology and Ecology, 407(2), 284-293, https://doi.org/10.1016/j.jembe.2011.06.027
Bögner, Desislava; Bickmeyer, Ulf; Köhler, Angela (2014): CO2-induced fertilization impairment in Strongylocentrotus droebachiensis collected in the Arctic. Helgoland Marine Research, 68(2), 341-356, https://doi.org/10.1007/s10152-014-0394-3
Borchard, Corinna; Borges, Alberto Vieira; Händel, Nicole; Engel, Anja (2011): Biogeochemical response of Emiliania huxleyi (PML B92/11) to elevated CO2 and temperature under phosphorous limitation: A chemostat study. Journal of Experimental Marine Biology and Ecology, 410, 61-71, https://doi.org/10.1016/j.jembe.2011.10.004
Borchard, Corinna; Engel, Anja (2012): Organic matter exudation by Emiliania huxleyi under simulated future ocean conditions. Biogeosciences, 9(8), 3405-3423, https://doi.org/10.5194/bg-9-3405-2012
Boucher, Guy; Clavier, Jacques; Garrigue, Claire (1994): Oxygen and carbon dioxide fluxes at the water-sediment interface of a tropical lagoon. Marine Ecology Progress Series, 107, 185-193, https://doi.org/10.3354/meps107185
Brading, Patrick; Warner, Mark E; Davey, Philip; Smith, David J; Achterberg, Eric Pieter; Suggett, David J (2011): Differential effects of ocean acidification on growth and photosynthesis among phylotypes of Symbiodinium (Dinophyceae). Limnology and Oceanography, 56(3), 927-938, https://doi.org/10.4319/lo.2011.56.3.0927
Braeckman, Ulrike; Van Colen, Carl; Guilini, Katja; Van Gansbeke, D; Soetaert, Karline; Vincx, Magda; Vanaverbeke, Jan; Vopel, Kay (2014): Empirical Evidence Reveals Seasonally Dependent Reduction in Nitrification in Coastal Sediments Subjected to Near Future Ocean Acidification. PLoS ONE, 9(10), e108153, https://doi.org/10.1371/journal.pone.0108153.s002
Bramanti, Lorenzo; Movilla, Juancho; Guron, Maricel; Calvo, Eva; Gori, Andrea; Dominguez-Cariò, Carlos; Grinyó, Jordi; Lopez-Sanz, Angel; Martinez-Quintana, Angela; Pelejero, Carles; Ziveri, Patrizia; Rossi, Sergio (2013): Detrimental effects of ocean acidification on the economically important Mediterranean red coral (Corallium rubrum). Global Change Biology, 19(6), 1897-1908, https://doi.org/10.1111/gcb.12171
Bray, Laura; Pancucci-Papadopulou, M A; Hall-Spencer, Jason M (2014): Sea urchin response to rising pCO2 shows ocean acidification may fundamentally alter the chemistry of marine skeletons. Mediterranean Marine Science, 15(3), 510-519, https://doi.org/10.12681/mms.579
Bresolin de Souza, Karine; Jutfelt, Fredrik; Kling, Peter; Förlin, Lars; Sturve, Joachim; Hofmann, Gretchen E (2014): Effects of Increased CO2 on Fish Gill and Plasma Proteome. PLoS ONE, 9(7), e102901, https://doi.org/10.1371/journal.pone.0102901
Bressan, M; Chinellato, A; Munari, M; Matozzo, V; Manci, A; Marceta, T; Finos, L; Moro, I; Pastore, P; Badocco, D; Marin, M G (2014): Does seawater acidification affect survival, growth and shell integrity in bivalve juveniles? Marine Environmental Research, 99, 136-148, https://doi.org/10.1016/j.marenvres.2014.04.009
Brussaard, Corina P D; Noordeloos, A A M; Witte, Hannelore; Collenteur, M C J; Schulz, Kai Georg; Ludwig, Andrea; Riebesell, Ulf (2013): Arctic microbial community dynamics influenced by elevated CO2 levels. Biogeosciences, 10(2), 719-731, https://doi.org/10.5194/bg-10-719-2013
Büdenbender, Jan; Riebesell, Ulf; Form, Armin (2011): Calcification of the Arctic coralline red algae Lithothamnion glaciale in response to elevated CO2. Marine Ecology Progress Series, 441, 79-87, https://doi.org/10.3354/meps09405
Burdett, H L; Carruthers, M; Donohue, P J C; Wicks, L C; Hennige, S J; Roberts, J Murray; Kamenos, N A (2014): Effects of high temperature and CO2 on intracellular DMSP in the cold-water coral Lophelia pertusa. Marine Biology, 161(7), 1499-1506, https://doi.org/10.1007/s00227-014-2435-5
Burkhardt, Steffen; Riebesell, Ulf; Zondervan, Ingrid (1999): Stable carbon isotope fractionation by marine phytoplankton in response to daylength, growth rate, and CO2 availability. Marine Ecology Progress Series, 194, 31-41, https://doi.org/10.3354/meps184031
Campbell, Justin E; Fourqurean, James W (2013): Effects of in situ CO2 enrichment on the structural and chemical characteristics of the seagrass Thalassia testudinum. Marine Biology, 160(6), 1465-1475, https://doi.org/10.1007/s00227-013-2199-3
Campbell, Justin E; Fourqurean, James W (2014): Ocean acidification outweighs nutrient effects in structuring seagrass epiphyte communities. Journal of Ecology, 102(3), 730-737, https://doi.org/10.1111/1365-2745.12233
Carey, Nicholas; Dupont, Sam; Lundve, Bengt; Sigwart, Julia D (2014): One size fits all: stability of metabolic scaling under warming and ocean acidification in echinoderms. Marine Biology, 161(9), 2131-2142, https://doi.org/10.1007/s00227-014-2493-8
Carey, Nicholas; Sigwart, Julia D (2014): Size matters: plasticity in metabolic scaling shows body-size may modulate responses to climate change. Biology Letters, 10(8), 20140408-20140408, https://doi.org/10.1098/rsbl.2014.0408
Challener, Roberta C; McClintock, James B; Makowsky, Robert (2013): Effects of reduced carbonate saturation state on early development in the common edible sea urchin Lytechinus variegatus: implications for land-based aquaculture. Journal of Applied Aquaculture, 25(2), 154-175, https://doi.org/10.1080/10454438.2013.791911
Challener, Roberta C; Watts, Stephen A; McClintock, James B (2014): Effects of hypercapnia on aspects of feeding, nutrition, and growth in the edible sea urchin Lytechinus variegatus held in culture. Marine and Freshwater Behaviour and Physiology, 47(1), 41-62, https://doi.org/10.1080/10236244.2013.875273
Chan, B S Vera; Li, Chaoyi; Lane, Ackley Charles; Wang, Yanchun; Lu, Xingwen; Shih, Kaimin; Zhang, Tong; Thiyagarajan, Vengatesen (2012): CO2-Driven Ocean Acidification Alters and Weakens Integrity of the Calcareous Tubes Produced by the Serpulid Tubeworm, Hydroides elegans. PLoS ONE, 7(8), e42718, https://doi.org/10.1371/journal.pone.0042718
Chan, B S Vera; Thiyagarajan, Vengatesen; Lu, Xingwen; Zhang, Tong; Shih, Kaimin (2013): Temperature Dependent Effects of Elevated CO2 on Shell Composition and Mechanical Properties of Hydroides elegans: Insights from a Multiple Stressor Experiment. PLoS ONE, 8(11), e78945, https://doi.org/10.1371/journal.pone.0078945
Chan, Kit Yu Karen; Grünbaum, Daniel; Arnberg, Maj; Thorndyke, Mike; Dupont, Sam (2012): Ocean acidification induces budding in larval sea urchins. Marine Biology, 160(8), 2129-2135, https://doi.org/10.1007/s00227-012-2103-6
Chan, Kit Yu Karen; Grünbaum, Daniel; O'Donnell, Michael J (2011): Effects of ocean-acidification-induced morphological changes on larval swimming and feeding. Journal of Experimental Biology, 214(22), 3857-3867, https://doi.org/10.1242/jeb.054809
Charalampopoulou, Anastasia; Poulton, Alex J; Tyrrell, Toby; Lucas, Mike (2011): Irradiance and pH affect coccolithophore community composition on a transect between the North Sea and the Arctic Ocean. Marine Ecology Progress Series, 431, 25-43, https://doi.org/10.3354/meps09140
Chauvin, Anne; Denis, Vianney; Cuet, Pascale (2011): Is the response of coral calcification to seawater acidification related to nutrient loading? Coral Reefs, 30(4), 911-923, https://doi.org/10.1007/s00338-011-0786-7
Checkley, David M; Dickson, Andrew G; Takahashi, Motomitsu; Radich, J Adam; Eisenkolb, Nadine; Asch, Rebecca (2009): Elevated CO2 enhances otolith growth in young fish. Science, 324(5935), 1683, https://doi.org/10.1126/science.1169806
Christen, Nadja; Calosi, Piero; McNeill, C L; Widdicombe, Stephen (2012): Structural and functional vulnerability to elevated pCO2 in marine benthic communities. Marine Biology, 160(8), 2113-2128, https://doi.org/10.1007/s00227-012-2097-0
Clark, Darren; Brown, Ian; Rees, Andrew; Somerfield, Paul J; Miller, P I (2014): The influence of ocean acidification on nitrogen regeneration and nitrous oxide production in the northwest European shelf sea. Biogeosciences, 11(18), 4985-5005, https://doi.org/10.5194/bg-11-4985-2014
Clavier, Jacques; Boucher, Guy; Garrigue, Claire (1994): Benthic respiratory and photosynthetic quotients in a tropical lagoon. Comptes Rendus de l'Académie des Sciences - Series III - Sciences de la Vie, 317, 937-942, hdl:10013/epic.34198.d001
Clements, Jeff C; Hunt, Heather L (2014): Influence of sediment acidification and water flow on sediment acceptance and dispersal of juvenile soft-shell clams (Mya arenaria L.). Journal of Experimental Marine Biology and Ecology, 453, 62-69, https://doi.org/10.1016/j.jembe.2014.01.002
Collard, Marie; Catarino, Ana Isabel; Bonnet, Stéphanie; Flammang, Patrick; Dubois, Philippe (2013): Effects of CO2-induced ocean acidification on physiological and mechanical properties of the starfish Asterias rubens. Journal of Experimental Marine Biology and Ecology, 446, 355-362, https://doi.org/10.1016/j.jembe.2013.06.003
Collard, Marie; De Ridder, Chantal; David, Bruno; Dehairs, Frank; Dubois, Philippe (2014): Could the acid-base status of Antarctic sea urchins indicate a better-than-expected resilience to near-future ocean acidification? Global Change Biology, https://doi.org/10.1111/gcb.12735
Collard, Marie; Dery, Aurélie; Dehairs, Frank; Dubois, Philippe (2014): Euechinoidea and Cidaroidea respond differently to ocean acidification. Comparative Biochemistry and Physiology Part A: Molecular & Integrative Physiology, 174, 45-55, https://doi.org/10.1016/j.cbpa.2014.04.011
Collard, Marie; Eeckhaut, Igor; Dehairs, Frank; Dubois, Philippe (2014): Acid–base physiology response to ocean acidification of two ecologically and economically important holothuroids from contrasting habitats, Holothuria scabra and Holothuria parva. Environmental Science and Pollution Research, 21(23), 13602-13614, https://doi.org/10.1007/s11356-014-3259-z
Collard, Marie; Laitat, Kim; Moulin, Laure; Catarino, Ana Isabel; Grosjean, Philippe; Dubois, Philippe (2013): Buffer capacity of the coelomic fluid in echinoderms. Comparative Biochemistry and Physiology Part A: Molecular & Integrative Physiology, 166(1), 199-206, https://doi.org/10.1016/j.cbpa.2013.06.002
Comeau, Steeve; Alliouane, Samir; Gattuso, Jean-Pierre (2012): Effects of ocean acidification on overwintering juvenile Arctic pteropods Limacina helicina. Marine Ecology Progress Series, 456, 279-284, https://doi.org/10.3354/meps09696
Comeau, Steeve; Carpenter, Robert C; Edmunds, Peter J (2012): Coral reef calcifiers buffer their response to ocean acidification using both bicarbonate and carbonate. Proceedings of the Royal Society B-Biological Sciences, 280(1753), https://doi.org/10.1098/rspb.2012.2374
Comeau, Steeve; Carpenter, Robert C; Edmunds, Peter J (2013): Effects of feeding and light intensity on the response of the coral Porites rus to ocean acidification. Marine Biology, 160(5), 1127-1134, https://doi.org/10.1007/s00227-012-2165-5
Comeau, Steeve; Carpenter, Robert C; Nojiri, Yukihiro; Putnam, H M; Sakai, Kazuhiko; Edmunds, Peter J (2014): Pacific-wide contrast highlights resistance of reef calcifiers to ocean acidification. Proceedings of the Royal Society B-Biological Sciences, 281(1790), 20141339-20141339, https://doi.org/10.1098/rspb.2014.1339
Comeau, Steeve; Edmunds, Peter J; Spindel, N B; Carpenter, Robert C (2014): Fast coral reef calcifiers are more sensitive to ocean acidification in short-term laboratory incubations. Limnology and Oceanography, 59(3), 1081-1091, https://doi.org/10.4319/lo.2014.59.3.1081
Comeau, Steeve; Edmunds, Peter J; Spindel, N B; Carpenter, Robert C (2013): The responses of eight coral reef calcifiers to increasing partial pressure of CO2 do not exhibit a tipping point. Limnology and Oceanography, 58(1), 388-398, https://doi.org/10.4319/lo.2013.58.1.0388
Comeau, Steeve; Gorsky, Gabriel; Alliouane, Samir; Gattuso, Jean-Pierre (2010): Larvae of the pteropod Cavolinia inflexa exposed to aragonite undersaturation are viable but shell-less. Marine Biology, 157(10), 2341-2345, https://doi.org/10.1007/s00227-010-1493-6
Comeau, Steeve; Gorsky, Gabriel; Jeffree, Ross; Teyssié, Jean-Louis; Gattuso, Jean-Pierre (2009): Impact of ocean acidification on a key Arctic pelagic mollusc (Limacina helicina). Biogeosciences, 6(9), 1877-1882, https://doi.org/10.5194/bg-6-1877-2009
Comeau, Steeve; Jeffree, Ross; Teyssié, Jean-Louis; Gattuso, Jean-Pierre (2010): Response of the Arctic pteropod Limacina helicina to projected future environmental conditions. PLoS ONE, 5(6), e11362, https://doi.org/10.1371/journal.pone.0011362
Connell, Sean D; Russell, Bayden D (2010): The direct effects of increasing CO2 and temperature on non-calcifying organisms: increasing the potential for phase shifts in kelp forests. Proceedings of the Royal Society B-Biological Sciences, 277(1686), 1409-1415, https://doi.org/10.1098/rspb.2009.2069
Cornwall, Christopher E; Boyd, Philip W; McGraw, Christina M; Hepburn, Christopher D; Pilditch, Conrad A; Morris, Jaz N; Smith, Abigail M;