Articles | Volume 12, issue 14
https://doi.org/10.5194/bg-12-4209-2015
© Author(s) 2015. This work is distributed under
the Creative Commons Attribution 3.0 License.
the Creative Commons Attribution 3.0 License.
https://doi.org/10.5194/bg-12-4209-2015
© Author(s) 2015. This work is distributed under
the Creative Commons Attribution 3.0 License.
the Creative Commons Attribution 3.0 License.
Impact of seawater carbonate chemistry on the calcification of marine bivalves
J. Thomsen
CORRESPONDING AUTHOR
Marine Ecology, GEOMAR Helmholtz Centre for Ocean Research, Kiel, Germany
Marine Biology Research Division, Scripps Institution of Oceanography, University of California, San Diego, La Jolla, CA 93092-0202, USA
K. Haynert
Marine Ecology, GEOMAR Helmholtz Centre for Ocean Research, Kiel, Germany
J. F. Blumenbach Institute for Zoology and Anthropology, Georg August University Göttingen, 37073 Göttingen, Germany
K. M. Wegner
Alfred Wegener Institute, Helmholtz Centre for Polar and Marine Research, Wadden Sea Station Sylt, 25992 List, Germany
F. Melzner
Marine Ecology, GEOMAR Helmholtz Centre for Ocean Research, Kiel, Germany
Viewed
Total article views: 6,701 (including HTML, PDF, and XML)
Cumulative views and downloads
(calculated since 22 Jan 2015)
| HTML | XML | Total | Supplement | BibTeX | EndNote | |
|---|---|---|---|---|---|---|
| 3,407 | 2,908 | 386 | 6,701 | 663 | 214 | 267 |
- HTML: 3,407
- PDF: 2,908
- XML: 386
- Total: 6,701
- Supplement: 663
- BibTeX: 214
- EndNote: 267
Total article views: 5,462 (including HTML, PDF, and XML)
Cumulative views and downloads
(calculated since 17 Jul 2015)
| HTML | XML | Total | Supplement | BibTeX | EndNote | |
|---|---|---|---|---|---|---|
| 2,880 | 2,223 | 359 | 5,462 | 403 | 192 | 238 |
- HTML: 2,880
- PDF: 2,223
- XML: 359
- Total: 5,462
- Supplement: 403
- BibTeX: 192
- EndNote: 238
Total article views: 1,239 (including HTML, PDF, and XML)
Cumulative views and downloads
(calculated since 22 Jan 2015)
| HTML | XML | Total | BibTeX | EndNote | |
|---|---|---|---|---|---|
| 527 | 685 | 27 | 1,239 | 22 | 29 |
- HTML: 527
- PDF: 685
- XML: 27
- Total: 1,239
- BibTeX: 22
- EndNote: 29
Cited
100 citations as recorded by crossref.
- Extinction risk related to functional traits in Pliocene to Holocene West Atlantic molluscs A. Betz et al. https://doi.org/10.1111/pala.70046
- Effect of CO2–induced ocean acidification on the early development and shell mineralization of the European abalone (Haliotis tuberculata) N. Wessel et al. https://doi.org/10.1016/j.jembe.2018.08.005
- The combined effects of salinity and pH on shell biomineralization of the edible mussel Mytilus chilensis C. Grenier et al. https://doi.org/10.1016/j.envpol.2020.114555
- Transcriptome and lipidome integration unveils key mechanisms constraining bivalve larval sensitivity in an acidifying sea Y. Xu et al. https://doi.org/10.1016/j.cbd.2025.101450
- Consideration of coastal carbonate chemistry in understanding biological calcification A. Fassbender et al. https://doi.org/10.1002/2016GL068860
- Bivalve shell formation in a naturally CO2-enriched habitat: Unraveling the resilience mechanisms from elemental signatures L. Zhao et al. https://doi.org/10.1016/j.chemosphere.2018.03.180
- Multiple carbonate system parameters independently govern shell formation in a marine mussel A. Ninokawa et al. https://doi.org/10.1038/s43247-024-01440-5
- Ocean acidification stress index for shellfish (OASIS): Linking Pacific oyster larval survival and exposure to variable carbonate chemistry regimes I. Gimenez et al. https://doi.org/10.1525/elementa.306
- Impact of seawater carbonate variables on post-larval bivalve calcification J. Li et al. https://doi.org/10.1007/s00343-017-6277-0
- Comparative de novo assembly and annotation of mantle tissue transcriptomes from the Mytilus edulis species complex (M. edulis, M. galloprovincialis, M. trossulus) L. Knöbel et al. https://doi.org/10.1016/j.margen.2019.100700
- Can seagrass modify the effects of ocean acidification on oysters? N. Garner et al. https://doi.org/10.1016/j.marpolbul.2022.113438
- A pronounced fall in the CaCO3 saturation state and the total alkalinity of the surface ocean during the Mid Mesozoic G. Aloisi https://doi.org/10.1016/j.chemgeo.2018.04.014
- Ocean acidification and warming modify stimulatory benthos effects on sediment functioning: An experimental study on two ecosystem engineers E. Vlaminck et al. https://doi.org/10.3389/fmars.2023.1101972
- Boosted nutritional quality of food by CO2 enrichment fails to offset energy demand of herbivores under ocean warming, causing energy depletion and mortality J. Leung et al. https://doi.org/10.1016/j.scitotenv.2018.05.161
- Biochemical alterations induced in Hediste diversicolor under seawater acidification conditions R. Freitas et al. https://doi.org/10.1016/j.marenvres.2016.04.003
- Biological and physiological responses of marine crabs to ocean acidification: A review S. Thangal et al. https://doi.org/10.1016/j.envres.2024.118238
- Biological modification of seawater chemistry by an ecosystem engineer, the California mussel,Mytilus californianus A. Ninokawa et al. https://doi.org/10.1002/lno.11258
- Transgenerational biochemical effects of seawater acidification on the Manila clam (Ruditapes philippinarum) L. Zhao et al. https://doi.org/10.1016/j.scitotenv.2019.136420
- Transcriptomic insights into cessation of clam embryonic development following transgenerational exposure to ocean acidity extreme Y. Xu et al. https://doi.org/10.1016/j.marenvres.2024.106561
- The dynamic ocean acidification manipulation experimental system: Separating carbonate variables and simulating natural variability in laboratory flow‐through experiments I. Gimenez et al. https://doi.org/10.1002/lom3.10318
- Expression of calcification‐related ion transporters during blue mussel larval development K. Ramesh et al. https://doi.org/10.1002/ece3.5287
- Physiological responses to ocean acidification and warming synergistically reduce condition of the common cockle Cerastoderma edule E. Ong et al. https://doi.org/10.1016/j.marenvres.2017.07.001
- Intra-population variability of ocean acidification impacts on the physiology of Baltic blue mussels (Mytilus edulis): integrating tissue and organism response L. Stapp et al. https://doi.org/10.1007/s00360-016-1053-6
- Moderate Increase in TCO2 Enhances Photosynthesis of Seagrass Zostera japonica, but Not Zostera marina: Implications for Acidification Mitigation C. Miller et al. https://doi.org/10.3389/fmars.2017.00228
- Measurement, Spatiotemporal Evolution, and Spatial Spillover Effects of Carbon Sinks and Emissions from Shellfish and Algae Mariculture in China H. Zeng et al. https://doi.org/10.3390/fishes10070301
- Benthic macrofaunal carbon fluxes and environmental drivers of spatial variability in a large coastal-plain estuary S. Ajayi et al. https://doi.org/10.5194/bg-22-7769-2025
- Mechanisms to Explain the Elemental Composition of the Initial Aragonite Shell of Larval Oysters B. Haley et al. https://doi.org/10.1002/2017GC007133
- Seasonal variation in aragonite saturation in surface waters of Puget Sound – a pilot study G. Pelletier et al. https://doi.org/10.1525/elementa.270
- Biomineralization and biomechanical trade-offs under heterogeneous environments in the eastern oyster Crassostrea virginica L. Telesca et al. https://doi.org/10.1093/mollus/eyae033
- Biomineralization plasticity and environmental heterogeneity predict geographical resilience patterns of foundation species to future change L. Telesca et al. https://doi.org/10.1111/gcb.14758
- Calcification in a marginal sea – influence of seawater [Ca2+] and carbonate chemistry on bivalve shell formation J. Thomsen et al. https://doi.org/10.5194/bg-15-1469-2018
- CMEMS-LSCE: a global, 0.25°, monthly reconstruction of the surface ocean carbonate system T. Chau et al. https://doi.org/10.5194/essd-16-121-2024
- Evidence for Carbonate System Mediated Shape Shift in an Intertidal Predatory Gastropod D. Mayk et al. https://doi.org/10.3389/fmars.2022.894182
- Intrinsic over extrinsic: Species identity shapes spatial and interannual Mg/Ca patterns in Arctic marine calcifiers M. Krzemińska et al. https://doi.org/10.1371/journal.pone.0345703
- Shell thickness of Nucella lapillus in the North Sea increased over the last 130 years despite ocean acidification D. Mayk et al. https://doi.org/10.1038/s43247-022-00486-7
- Organic matter processing in a [simulated] offshore wind farm ecosystem in current and future climate and aquaculture scenarios H. Voet et al. https://doi.org/10.1016/j.scitotenv.2022.159285
- Mineralogical and geochemical composition of CaCO3 skeletons secreted by benthic invertebrates from the brackish Baltic Sea A. Piwoni-Piórewicz et al. https://doi.org/10.1016/j.ecss.2022.107808
- Macroalgae may mitigate ocean acidification effects on mussel calcification by increasing pH and its fluctuations M. Wahl et al. https://doi.org/10.1002/lno.10608
- Size matters: Physiological sensitivity of the scallop Argopecten purpuratus to seasonal cooling and deoxygenation upwelling-driven events L. Ramajo et al. https://doi.org/10.3389/fmars.2022.992319
- Removal of dissolved inorganic carbon from seawater for climate mitigation: potential marine ecosystem impacts G. Hooper et al. https://doi.org/10.3389/fclim.2025.1528951
- Shifting Balance of Protein Synthesis and Degradation Sets a Threshold for Larval Growth Under Environmental Stress C. Frieder et al. https://doi.org/10.1086/696830
- Effects of food supply on northern bay scallops Argopecten irradians reared under two pCO2 conditions S. Gurr et al. https://doi.org/10.3354/meps14624
- A mineralogical record of ocean change: Decadal and centennial patterns in the California mussel S. McCoy et al. https://doi.org/10.1111/gcb.14013
- Combined effects of salinity and trematode infections on the filtration capacity, growth and condition of mussels C. Bommarito et al. https://doi.org/10.3354/meps14179
- Seawater carbonate parameters function differently in affecting embryonic development and calcification in Pacific abalone (Haliotis discus hannai) J. Li et al. https://doi.org/10.1016/j.aquatox.2023.106450
- Naturally acidified habitat selects for ocean acidification–tolerant mussels J. Thomsen et al. https://doi.org/10.1126/sciadv.1602411
- Impaired larval development at low salinities could limit the spread of the non-native crab Hemigrapsus takanoi in the Baltic Sea O. Nour et al. https://doi.org/10.3354/ab00743
- Ocean Acidification and Coastal Marine Invertebrates: Tracking CO2Effects from Seawater to the Cell F. Melzner et al. https://doi.org/10.1146/annurev-marine-010419-010658
- Physiological response to seawater pH of the bivalve Abra alba, a benthic ecosystem engineer, is modulated by low pH E. Vlaminck et al. https://doi.org/10.1016/j.marenvres.2022.105704
- Shell Proteome Plasticity Assists Oyster Larval Biomineralization in Adverse Carbonate Chemistry A. Carini et al. https://doi.org/10.1002/jezb.70003
- FINE STRUCTURE OF THE SHELL OF DIPLOID AND TRIPLOID OYSTERS, <i>CRASSOSTREA GIGAS</i> (THUNBERG 1793) (BIVALVIA, OSTREIDAE) REARED IN THE BLACK SEA A. Pirkova & L. Ladygina https://doi.org/10.31857/S004451342309009X
- Olivine and dissolved alkalinity trigger different bacterial community shifts in water and oyster gills: insights from a mesocosm experiment D. Antoni et al. https://doi.org/10.3389/frmbi.2025.1659695
- Recommended priorities for research on ecological impacts of ocean and coastal acidification in the U.S. Mid-Atlantic G. Saba et al. https://doi.org/10.1016/j.ecss.2019.04.022
- Fractionation, bioavailability and risk evaluation of phosphorus in lagoons surface sediments, Red Sea, Saudi Arabia B. Al-Mur https://doi.org/10.1080/02757540.2023.2222020
- Microbiome response differs among selected lines of Sydney rock oysters to ocean warming and acidification E. Scanes et al. https://doi.org/10.1093/femsec/fiab099
- The Fine Structure of the Shell of Diploid and Triploid Oysters, Crassostrea gigas (Thunberg 1793) (Bivalvia, Ostreidae), Raised in the Black Sea A. Pirkova & L. Ladygina https://doi.org/10.1134/S1062359024700511
- Legacy of Multiple Stressors: Responses of Gastropod Larvae and Juveniles to Ocean Acidification and Nutrition S. Bogan et al. https://doi.org/10.1086/702993
- Deciphering carbon sources of mussel shell carbonate under experimental ocean acidification and warming Y. Lu et al. https://doi.org/10.1016/j.marenvres.2018.10.007
- Transgenerational acclimation to seawater acidification in the Manila clam Ruditapes philippinarum: Preferential uptake of metabolic carbon L. Zhao et al. https://doi.org/10.1016/j.scitotenv.2018.01.225
- Ocean acidification impacts growth and shell mineralization in juvenile abalone (Haliotis tuberculata) S. Auzoux-Bordenave et al. https://doi.org/10.1007/s00227-019-3623-0
- Effects of carbamazepine and cetirizine under an ocean acidification scenario on the biochemical and transcriptome responses of the clam Ruditapes philippinarum Â. Almeida et al. https://doi.org/10.1016/j.envpol.2017.12.121
- Water quality and the CO2-carbonate system during the preconditioning of Pacific oyster (Crassostrea gigas) in a recirculating aquaculture system S. Villasuso-Palomares et al. https://doi.org/10.1038/s41598-022-26661-6
- Persistent spatial structuring of coastal ocean acidification in the California Current System F. Chan et al. https://doi.org/10.1038/s41598-017-02777-y
- Proteomic investigation of the blue mussel larval shell organic matrix A. Carini et al. https://doi.org/10.1016/j.jsb.2019.09.002
- Blue Mussel (Genus Mytilus) Transcriptome Response to Simulated Climate Change in the Gulf of Maine P. Martino et al. https://doi.org/10.2983/035.038.0310
- Ocean pH fluctuations affect mussel larvae at key developmental transitions L. Kapsenberg et al. https://doi.org/10.1098/rspb.2018.2381
- Calcium carbonate alters the functional response of coastal sediments to eutrophication-induced acidification T. Drylie et al. https://doi.org/10.1038/s41598-019-48549-8
- Standing genetic variation fuels rapid adaptation to ocean acidification M. Bitter et al. https://doi.org/10.1038/s41467-019-13767-1
- Dual-Lifetime Referencing (t-DLR) Optical Fiber Fluorescent pH Sensor for Microenvironments W. Chen et al. https://doi.org/10.3390/s23218865
- Radioisotopes for monitoring the effects of Climate Change on marine Ecosystems: The REMO/ClimOcean project at SPES/LNL RIB facility F. Zeng et al. https://doi.org/10.1051/epjconf/202534201032
- Impacts of ocean acidification in a warming Mediterranean Sea: An overview T. Lacoue-Labarthe et al. https://doi.org/10.1016/j.rsma.2015.12.005
- Ocean Acidification Alters Developmental Timing and Gene Expression of Ion Transport Proteins During Larval Development in Resilient and Susceptible Lineages of the Pacific Oyster (Crassostrea gigas) M. Wright-LaGreca et al. https://doi.org/10.1007/s10126-022-10090-7
- Metabolic cost of calcification in bivalve larvae under experimental ocean acidification C. Frieder et al. https://doi.org/10.1093/icesjms/fsw213
- Behavioural and eco-physiological responses of the mussel Mytilus galloprovincialis to acidification and distinct feeding regimes J. Lassoued et al. https://doi.org/10.3354/meps13075
- The effects of low seawater pH on energy storage and heat shock protein 70 expression in a bivalve Limecola balthica A. Sokołowski & D. Brulińska https://doi.org/10.1016/j.marenvres.2018.06.018
- Seagrass-driven changes in carbonate chemistry enhance oyster shell growth A. Ricart et al. https://doi.org/10.1007/s00442-021-04949-0
- Large-scale oyster farming accelerates the removal of dissolved inorganic carbon from seawater in Sanggou Bay J. Li et al. https://doi.org/10.1016/j.marenvres.2024.106798
- Combining hydrodynamic modelling with genetics: can passive larval drift shape the genetic structure of Baltic Mytilus populations? H. Stuckas et al. https://doi.org/10.1111/mec.14075
- In vivo characterization of bivalve larval shells: a confocal Raman microscopy study K. Ramesh et al. https://doi.org/10.1098/rsif.2017.0723
- Decoupling salinity and carbonate chemistry: low calcium ion concentration rather than salinity limits calcification in Baltic Sea mussels T. Sanders et al. https://doi.org/10.5194/bg-18-2573-2021
- Calmodulin regulates the calcium homeostasis in mantle of Crassostrea gigas under ocean acidification X. Xin et al. https://doi.org/10.3389/fmars.2022.1050022
- Reconsidering the role of carbonate ion concentration in calcification by marine organisms L. Bach https://doi.org/10.5194/bg-12-4939-2015
- Coupled ocean warming and acidification reduce shell integrity and bioenergetics in juvenile Mytilus coruscus B. Wang et al. https://doi.org/10.3354/meps15134
- The Biological Crystals in Chamid Bivalve Shells: Diversity in Morphology and Crystal Arrangement Pattern S. Hoerl et al. https://doi.org/10.3390/cryst14070649
- High Calcification Costs Limit Mussel Growth at Low Salinity T. Sanders et al. https://doi.org/10.3389/fmars.2018.00352
- In situ recovery of bivalve shell characteristics after temporary exposure to elevated pCO2 J. Grear et al. https://doi.org/10.1002/lno.11456
- Ocean acidification reduces hardness and stiffness of the Portuguese oyster shell with impaired microstructure: a hierarchical analysis Y. Meng et al. https://doi.org/10.5194/bg-15-6833-2018
- Living under natural conditions of ocean acidification entails energy expenditure and oxidative stress in a mussel species S. Signorini et al. https://doi.org/10.1016/j.marpolbul.2024.116470
- Acidification, warming, and nutrient management are projected to cause reductions in shell and tissue weights of oysters in a coastal plain estuary C. Czajka et al. https://doi.org/10.5194/bg-22-3181-2025
- CONSIDERATION OF THE VALIDITY OF THE STATISTICAL CHARACTERISTICS OF pH IN SURFACE WATERS V. Korobov et al. https://doi.org/10.25296/1997-8650-2019-13-2-52-58
- Combination of RNAseq and RADseq to Identify Physiological and Adaptive Responses to Acidification in the Eastern Oyster (Crassostrea virginica) C. Schwaner et al. https://doi.org/10.1007/s10126-023-10255-y
- Long-term alkalinity trends in the Baltic Sea and their implications for CO2 -induced acidification J. Müller et al. https://doi.org/10.1002/lno.10349
- Effects of ocean acidification on 109Cd, 57Co, and 134Cs bioconcentration by the European oyster (Ostrea edulis): Biokinetics and tissue-to-subcellular partitioning N. Sezer et al. https://doi.org/10.1016/j.jenvrad.2018.07.011
- Infection by invasive parasites increases susceptibility of native hosts to secondary infection via modulation of cellular immunity F. Demann et al. https://doi.org/10.1111/1365-2656.12939
- Dilution of Seawater Affects the Ca2 + Transport in the Outer Mantle Epithelium of Crassostrea gigas J. Sillanpää et al. https://doi.org/10.3389/fphys.2020.00001
- Vulnerability of Tritia reticulata (L.) early life stages to ocean acidification and warming I. Oliveira et al. https://doi.org/10.1038/s41598-020-62169-7
- Temperature and reduced pH regulate stress and biomineralization gene expression in larvae and post-larvae of the sand dollar Dendraster excentricus T. Olivares-Bañuelos et al. https://doi.org/10.1080/17451000.2022.2105894
- Clumped isotopes in modern marine bivalves D. Huyghe et al. https://doi.org/10.1016/j.gca.2021.09.019
- Impacts of Acclimation in Warm-Low pH Conditions on the Physiology of the Sea Urchin Heliocidaris erythrogramma and Carryover Effects for Juvenile Offspring J. Harianto et al. https://doi.org/10.3389/fmars.2020.588938
- A post-larval stage-based model of hard clam Mercenaria mercenaria development in response to multiple stressors: temperature and acidification severity C. Miller & G. Waldbusser https://doi.org/10.3354/meps11882
100 citations as recorded by crossref.
- Extinction risk related to functional traits in Pliocene to Holocene West Atlantic molluscs A. Betz et al. https://doi.org/10.1111/pala.70046
- Effect of CO2–induced ocean acidification on the early development and shell mineralization of the European abalone (Haliotis tuberculata) N. Wessel et al. https://doi.org/10.1016/j.jembe.2018.08.005
- The combined effects of salinity and pH on shell biomineralization of the edible mussel Mytilus chilensis C. Grenier et al. https://doi.org/10.1016/j.envpol.2020.114555
- Transcriptome and lipidome integration unveils key mechanisms constraining bivalve larval sensitivity in an acidifying sea Y. Xu et al. https://doi.org/10.1016/j.cbd.2025.101450
- Consideration of coastal carbonate chemistry in understanding biological calcification A. Fassbender et al. https://doi.org/10.1002/2016GL068860
- Bivalve shell formation in a naturally CO2-enriched habitat: Unraveling the resilience mechanisms from elemental signatures L. Zhao et al. https://doi.org/10.1016/j.chemosphere.2018.03.180
- Multiple carbonate system parameters independently govern shell formation in a marine mussel A. Ninokawa et al. https://doi.org/10.1038/s43247-024-01440-5
- Ocean acidification stress index for shellfish (OASIS): Linking Pacific oyster larval survival and exposure to variable carbonate chemistry regimes I. Gimenez et al. https://doi.org/10.1525/elementa.306
- Impact of seawater carbonate variables on post-larval bivalve calcification J. Li et al. https://doi.org/10.1007/s00343-017-6277-0
- Comparative de novo assembly and annotation of mantle tissue transcriptomes from the Mytilus edulis species complex (M. edulis, M. galloprovincialis, M. trossulus) L. Knöbel et al. https://doi.org/10.1016/j.margen.2019.100700
- Can seagrass modify the effects of ocean acidification on oysters? N. Garner et al. https://doi.org/10.1016/j.marpolbul.2022.113438
- A pronounced fall in the CaCO3 saturation state and the total alkalinity of the surface ocean during the Mid Mesozoic G. Aloisi https://doi.org/10.1016/j.chemgeo.2018.04.014
- Ocean acidification and warming modify stimulatory benthos effects on sediment functioning: An experimental study on two ecosystem engineers E. Vlaminck et al. https://doi.org/10.3389/fmars.2023.1101972
- Boosted nutritional quality of food by CO2 enrichment fails to offset energy demand of herbivores under ocean warming, causing energy depletion and mortality J. Leung et al. https://doi.org/10.1016/j.scitotenv.2018.05.161
- Biochemical alterations induced in Hediste diversicolor under seawater acidification conditions R. Freitas et al. https://doi.org/10.1016/j.marenvres.2016.04.003
- Biological and physiological responses of marine crabs to ocean acidification: A review S. Thangal et al. https://doi.org/10.1016/j.envres.2024.118238
- Biological modification of seawater chemistry by an ecosystem engineer, the California mussel,Mytilus californianus A. Ninokawa et al. https://doi.org/10.1002/lno.11258
- Transgenerational biochemical effects of seawater acidification on the Manila clam (Ruditapes philippinarum) L. Zhao et al. https://doi.org/10.1016/j.scitotenv.2019.136420
- Transcriptomic insights into cessation of clam embryonic development following transgenerational exposure to ocean acidity extreme Y. Xu et al. https://doi.org/10.1016/j.marenvres.2024.106561
- The dynamic ocean acidification manipulation experimental system: Separating carbonate variables and simulating natural variability in laboratory flow‐through experiments I. Gimenez et al. https://doi.org/10.1002/lom3.10318
- Expression of calcification‐related ion transporters during blue mussel larval development K. Ramesh et al. https://doi.org/10.1002/ece3.5287
- Physiological responses to ocean acidification and warming synergistically reduce condition of the common cockle Cerastoderma edule E. Ong et al. https://doi.org/10.1016/j.marenvres.2017.07.001
- Intra-population variability of ocean acidification impacts on the physiology of Baltic blue mussels (Mytilus edulis): integrating tissue and organism response L. Stapp et al. https://doi.org/10.1007/s00360-016-1053-6
- Moderate Increase in TCO2 Enhances Photosynthesis of Seagrass Zostera japonica, but Not Zostera marina: Implications for Acidification Mitigation C. Miller et al. https://doi.org/10.3389/fmars.2017.00228
- Measurement, Spatiotemporal Evolution, and Spatial Spillover Effects of Carbon Sinks and Emissions from Shellfish and Algae Mariculture in China H. Zeng et al. https://doi.org/10.3390/fishes10070301
- Benthic macrofaunal carbon fluxes and environmental drivers of spatial variability in a large coastal-plain estuary S. Ajayi et al. https://doi.org/10.5194/bg-22-7769-2025
- Mechanisms to Explain the Elemental Composition of the Initial Aragonite Shell of Larval Oysters B. Haley et al. https://doi.org/10.1002/2017GC007133
- Seasonal variation in aragonite saturation in surface waters of Puget Sound – a pilot study G. Pelletier et al. https://doi.org/10.1525/elementa.270
- Biomineralization and biomechanical trade-offs under heterogeneous environments in the eastern oyster Crassostrea virginica L. Telesca et al. https://doi.org/10.1093/mollus/eyae033
- Biomineralization plasticity and environmental heterogeneity predict geographical resilience patterns of foundation species to future change L. Telesca et al. https://doi.org/10.1111/gcb.14758
- Calcification in a marginal sea – influence of seawater [Ca2+] and carbonate chemistry on bivalve shell formation J. Thomsen et al. https://doi.org/10.5194/bg-15-1469-2018
- CMEMS-LSCE: a global, 0.25°, monthly reconstruction of the surface ocean carbonate system T. Chau et al. https://doi.org/10.5194/essd-16-121-2024
- Evidence for Carbonate System Mediated Shape Shift in an Intertidal Predatory Gastropod D. Mayk et al. https://doi.org/10.3389/fmars.2022.894182
- Intrinsic over extrinsic: Species identity shapes spatial and interannual Mg/Ca patterns in Arctic marine calcifiers M. Krzemińska et al. https://doi.org/10.1371/journal.pone.0345703
- Shell thickness of Nucella lapillus in the North Sea increased over the last 130 years despite ocean acidification D. Mayk et al. https://doi.org/10.1038/s43247-022-00486-7
- Organic matter processing in a [simulated] offshore wind farm ecosystem in current and future climate and aquaculture scenarios H. Voet et al. https://doi.org/10.1016/j.scitotenv.2022.159285
- Mineralogical and geochemical composition of CaCO3 skeletons secreted by benthic invertebrates from the brackish Baltic Sea A. Piwoni-Piórewicz et al. https://doi.org/10.1016/j.ecss.2022.107808
- Macroalgae may mitigate ocean acidification effects on mussel calcification by increasing pH and its fluctuations M. Wahl et al. https://doi.org/10.1002/lno.10608
- Size matters: Physiological sensitivity of the scallop Argopecten purpuratus to seasonal cooling and deoxygenation upwelling-driven events L. Ramajo et al. https://doi.org/10.3389/fmars.2022.992319
- Removal of dissolved inorganic carbon from seawater for climate mitigation: potential marine ecosystem impacts G. Hooper et al. https://doi.org/10.3389/fclim.2025.1528951
- Shifting Balance of Protein Synthesis and Degradation Sets a Threshold for Larval Growth Under Environmental Stress C. Frieder et al. https://doi.org/10.1086/696830
- Effects of food supply on northern bay scallops Argopecten irradians reared under two pCO2 conditions S. Gurr et al. https://doi.org/10.3354/meps14624
- A mineralogical record of ocean change: Decadal and centennial patterns in the California mussel S. McCoy et al. https://doi.org/10.1111/gcb.14013
- Combined effects of salinity and trematode infections on the filtration capacity, growth and condition of mussels C. Bommarito et al. https://doi.org/10.3354/meps14179
- Seawater carbonate parameters function differently in affecting embryonic development and calcification in Pacific abalone (Haliotis discus hannai) J. Li et al. https://doi.org/10.1016/j.aquatox.2023.106450
- Naturally acidified habitat selects for ocean acidification–tolerant mussels J. Thomsen et al. https://doi.org/10.1126/sciadv.1602411
- Impaired larval development at low salinities could limit the spread of the non-native crab Hemigrapsus takanoi in the Baltic Sea O. Nour et al. https://doi.org/10.3354/ab00743
- Ocean Acidification and Coastal Marine Invertebrates: Tracking CO2Effects from Seawater to the Cell F. Melzner et al. https://doi.org/10.1146/annurev-marine-010419-010658
- Physiological response to seawater pH of the bivalve Abra alba, a benthic ecosystem engineer, is modulated by low pH E. Vlaminck et al. https://doi.org/10.1016/j.marenvres.2022.105704
- Shell Proteome Plasticity Assists Oyster Larval Biomineralization in Adverse Carbonate Chemistry A. Carini et al. https://doi.org/10.1002/jezb.70003
- FINE STRUCTURE OF THE SHELL OF DIPLOID AND TRIPLOID OYSTERS, <i>CRASSOSTREA GIGAS</i> (THUNBERG 1793) (BIVALVIA, OSTREIDAE) REARED IN THE BLACK SEA A. Pirkova & L. Ladygina https://doi.org/10.31857/S004451342309009X
- Olivine and dissolved alkalinity trigger different bacterial community shifts in water and oyster gills: insights from a mesocosm experiment D. Antoni et al. https://doi.org/10.3389/frmbi.2025.1659695
- Recommended priorities for research on ecological impacts of ocean and coastal acidification in the U.S. Mid-Atlantic G. Saba et al. https://doi.org/10.1016/j.ecss.2019.04.022
- Fractionation, bioavailability and risk evaluation of phosphorus in lagoons surface sediments, Red Sea, Saudi Arabia B. Al-Mur https://doi.org/10.1080/02757540.2023.2222020
- Microbiome response differs among selected lines of Sydney rock oysters to ocean warming and acidification E. Scanes et al. https://doi.org/10.1093/femsec/fiab099
- The Fine Structure of the Shell of Diploid and Triploid Oysters, Crassostrea gigas (Thunberg 1793) (Bivalvia, Ostreidae), Raised in the Black Sea A. Pirkova & L. Ladygina https://doi.org/10.1134/S1062359024700511
- Legacy of Multiple Stressors: Responses of Gastropod Larvae and Juveniles to Ocean Acidification and Nutrition S. Bogan et al. https://doi.org/10.1086/702993
- Deciphering carbon sources of mussel shell carbonate under experimental ocean acidification and warming Y. Lu et al. https://doi.org/10.1016/j.marenvres.2018.10.007
- Transgenerational acclimation to seawater acidification in the Manila clam Ruditapes philippinarum: Preferential uptake of metabolic carbon L. Zhao et al. https://doi.org/10.1016/j.scitotenv.2018.01.225
- Ocean acidification impacts growth and shell mineralization in juvenile abalone (Haliotis tuberculata) S. Auzoux-Bordenave et al. https://doi.org/10.1007/s00227-019-3623-0
- Effects of carbamazepine and cetirizine under an ocean acidification scenario on the biochemical and transcriptome responses of the clam Ruditapes philippinarum Â. Almeida et al. https://doi.org/10.1016/j.envpol.2017.12.121
- Water quality and the CO2-carbonate system during the preconditioning of Pacific oyster (Crassostrea gigas) in a recirculating aquaculture system S. Villasuso-Palomares et al. https://doi.org/10.1038/s41598-022-26661-6
- Persistent spatial structuring of coastal ocean acidification in the California Current System F. Chan et al. https://doi.org/10.1038/s41598-017-02777-y
- Proteomic investigation of the blue mussel larval shell organic matrix A. Carini et al. https://doi.org/10.1016/j.jsb.2019.09.002
- Blue Mussel (Genus Mytilus) Transcriptome Response to Simulated Climate Change in the Gulf of Maine P. Martino et al. https://doi.org/10.2983/035.038.0310
- Ocean pH fluctuations affect mussel larvae at key developmental transitions L. Kapsenberg et al. https://doi.org/10.1098/rspb.2018.2381
- Calcium carbonate alters the functional response of coastal sediments to eutrophication-induced acidification T. Drylie et al. https://doi.org/10.1038/s41598-019-48549-8
- Standing genetic variation fuels rapid adaptation to ocean acidification M. Bitter et al. https://doi.org/10.1038/s41467-019-13767-1
- Dual-Lifetime Referencing (t-DLR) Optical Fiber Fluorescent pH Sensor for Microenvironments W. Chen et al. https://doi.org/10.3390/s23218865
- Radioisotopes for monitoring the effects of Climate Change on marine Ecosystems: The REMO/ClimOcean project at SPES/LNL RIB facility F. Zeng et al. https://doi.org/10.1051/epjconf/202534201032
- Impacts of ocean acidification in a warming Mediterranean Sea: An overview T. Lacoue-Labarthe et al. https://doi.org/10.1016/j.rsma.2015.12.005
- Ocean Acidification Alters Developmental Timing and Gene Expression of Ion Transport Proteins During Larval Development in Resilient and Susceptible Lineages of the Pacific Oyster (Crassostrea gigas) M. Wright-LaGreca et al. https://doi.org/10.1007/s10126-022-10090-7
- Metabolic cost of calcification in bivalve larvae under experimental ocean acidification C. Frieder et al. https://doi.org/10.1093/icesjms/fsw213
- Behavioural and eco-physiological responses of the mussel Mytilus galloprovincialis to acidification and distinct feeding regimes J. Lassoued et al. https://doi.org/10.3354/meps13075
- The effects of low seawater pH on energy storage and heat shock protein 70 expression in a bivalve Limecola balthica A. Sokołowski & D. Brulińska https://doi.org/10.1016/j.marenvres.2018.06.018
- Seagrass-driven changes in carbonate chemistry enhance oyster shell growth A. Ricart et al. https://doi.org/10.1007/s00442-021-04949-0
- Large-scale oyster farming accelerates the removal of dissolved inorganic carbon from seawater in Sanggou Bay J. Li et al. https://doi.org/10.1016/j.marenvres.2024.106798
- Combining hydrodynamic modelling with genetics: can passive larval drift shape the genetic structure of Baltic Mytilus populations? H. Stuckas et al. https://doi.org/10.1111/mec.14075
- In vivo characterization of bivalve larval shells: a confocal Raman microscopy study K. Ramesh et al. https://doi.org/10.1098/rsif.2017.0723
- Decoupling salinity and carbonate chemistry: low calcium ion concentration rather than salinity limits calcification in Baltic Sea mussels T. Sanders et al. https://doi.org/10.5194/bg-18-2573-2021
- Calmodulin regulates the calcium homeostasis in mantle of Crassostrea gigas under ocean acidification X. Xin et al. https://doi.org/10.3389/fmars.2022.1050022
- Reconsidering the role of carbonate ion concentration in calcification by marine organisms L. Bach https://doi.org/10.5194/bg-12-4939-2015
- Coupled ocean warming and acidification reduce shell integrity and bioenergetics in juvenile Mytilus coruscus B. Wang et al. https://doi.org/10.3354/meps15134
- The Biological Crystals in Chamid Bivalve Shells: Diversity in Morphology and Crystal Arrangement Pattern S. Hoerl et al. https://doi.org/10.3390/cryst14070649
- High Calcification Costs Limit Mussel Growth at Low Salinity T. Sanders et al. https://doi.org/10.3389/fmars.2018.00352
- In situ recovery of bivalve shell characteristics after temporary exposure to elevated pCO2 J. Grear et al. https://doi.org/10.1002/lno.11456
- Ocean acidification reduces hardness and stiffness of the Portuguese oyster shell with impaired microstructure: a hierarchical analysis Y. Meng et al. https://doi.org/10.5194/bg-15-6833-2018
- Living under natural conditions of ocean acidification entails energy expenditure and oxidative stress in a mussel species S. Signorini et al. https://doi.org/10.1016/j.marpolbul.2024.116470
- Acidification, warming, and nutrient management are projected to cause reductions in shell and tissue weights of oysters in a coastal plain estuary C. Czajka et al. https://doi.org/10.5194/bg-22-3181-2025
- CONSIDERATION OF THE VALIDITY OF THE STATISTICAL CHARACTERISTICS OF pH IN SURFACE WATERS V. Korobov et al. https://doi.org/10.25296/1997-8650-2019-13-2-52-58
- Combination of RNAseq and RADseq to Identify Physiological and Adaptive Responses to Acidification in the Eastern Oyster (Crassostrea virginica) C. Schwaner et al. https://doi.org/10.1007/s10126-023-10255-y
- Long-term alkalinity trends in the Baltic Sea and their implications for CO2 -induced acidification J. Müller et al. https://doi.org/10.1002/lno.10349
- Effects of ocean acidification on 109Cd, 57Co, and 134Cs bioconcentration by the European oyster (Ostrea edulis): Biokinetics and tissue-to-subcellular partitioning N. Sezer et al. https://doi.org/10.1016/j.jenvrad.2018.07.011
- Infection by invasive parasites increases susceptibility of native hosts to secondary infection via modulation of cellular immunity F. Demann et al. https://doi.org/10.1111/1365-2656.12939
- Dilution of Seawater Affects the Ca2 + Transport in the Outer Mantle Epithelium of Crassostrea gigas J. Sillanpää et al. https://doi.org/10.3389/fphys.2020.00001
- Vulnerability of Tritia reticulata (L.) early life stages to ocean acidification and warming I. Oliveira et al. https://doi.org/10.1038/s41598-020-62169-7
- Temperature and reduced pH regulate stress and biomineralization gene expression in larvae and post-larvae of the sand dollar Dendraster excentricus T. Olivares-Bañuelos et al. https://doi.org/10.1080/17451000.2022.2105894
- Clumped isotopes in modern marine bivalves D. Huyghe et al. https://doi.org/10.1016/j.gca.2021.09.019
- Impacts of Acclimation in Warm-Low pH Conditions on the Physiology of the Sea Urchin Heliocidaris erythrogramma and Carryover Effects for Juvenile Offspring J. Harianto et al. https://doi.org/10.3389/fmars.2020.588938
- A post-larval stage-based model of hard clam Mercenaria mercenaria development in response to multiple stressors: temperature and acidification severity C. Miller & G. Waldbusser https://doi.org/10.3354/meps11882
Saved (final revised paper)
Latest update: 04 Jun 2026
Altmetrics
Final-revised paper
Preprint