105 citations as recorded by crossref.

1. Extinction risk related to functional traits in Pliocene to Holocene West Atlantic molluscs A. Betz et al. https://doi.org/10.1111/pala.70046
2. 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
3. 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
4. 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
5. Microhabitat-driven variation in predator–prey interactions between the crab Acanthocyclus hassleri and the mussel Perumytilus purpuratus E. Sabja-Llanos et al. https://doi.org/10.1016/j.jembe.2026.152229
6. Consideration of coastal carbonate chemistry in understanding biological calcification A. Fassbender et al. https://doi.org/10.1002/2016GL068860
7. 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
8. 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
9. 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
10. Impact of seawater carbonate variables on post-larval bivalve calcification J. Li et al. https://doi.org/10.1007/s00343-017-6277-0
11. 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
12. Submarine groundwater discharge drives massive carbon outwelling and impacts ocean acidification buffering in a mangrove-dominated bay of the Beibu Gulf, China H. Li et al. https://doi.org/10.1007/s13131-025-2616-8
13. Can seagrass modify the effects of ocean acidification on oysters? N. Garner et al. https://doi.org/10.1016/j.marpolbul.2022.113438
14. 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
15. 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
16. 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
17. Biochemical alterations induced in Hediste diversicolor under seawater acidification conditions R. Freitas et al. https://doi.org/10.1016/j.marenvres.2016.04.003
18. 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
19. 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
20. 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
21. 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
22. 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
23. Expression of calcification‐related ion transporters during blue mussel larval development K. Ramesh et al. https://doi.org/10.1002/ece3.5287
24. 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
25. 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
26. 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
27. 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
28. 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
29. Mechanisms to Explain the Elemental Composition of the Initial Aragonite Shell of Larval Oysters B. Haley et al. https://doi.org/10.1002/2017GC007133
30. 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
31. 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
32. 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
33. 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
34. 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
35. Bioturbation Under Stress: Linking Coastal Environmental Change to the Physiology and Function of Marine Bioturbators L. Gottschalck et al. https://doi.org/10.1007/s12237-026-01807-1
36. Evidence for Carbonate System Mediated Shape Shift in an Intertidal Predatory Gastropod D. Mayk et al. https://doi.org/10.3389/fmars.2022.894182
37. 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
38. 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
39. 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
40. 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
41. 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
42. 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
43. 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
44. 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
45. 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
46. 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
47. 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
48. 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
49. Naturally acidified habitat selects for ocean acidification–tolerant mussels J. Thomsen et al. https://doi.org/10.1126/sciadv.1602411
50. 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
51. 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
52. 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
53. Shell Proteome Plasticity Assists Oyster Larval Biomineralization in Adverse Carbonate Chemistry A. Carini et al. https://doi.org/10.1002/jezb.70003
54. 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
55. 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
56. 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
57. 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
58. 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
59. 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
60. 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
61. 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
62. 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
63. Refinement of Habitat‐Based Taxonomic Inventories for Benthic Macroinvertebrates: A Focus on Inland Water Ecosystem Surveys Y. Jun et al. https://doi.org/10.1111/1748-5967.70141
64. 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
65. 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
66. 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
67. 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
68. Proteomic investigation of the blue mussel larval shell organic matrix A. Carini et al. https://doi.org/10.1016/j.jsb.2019.09.002
69. 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
70. Ocean pH fluctuations affect mussel larvae at key developmental transitions L. Kapsenberg et al. https://doi.org/10.1098/rspb.2018.2381
71. 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
72. Standing genetic variation fuels rapid adaptation to ocean acidification M. Bitter et al. https://doi.org/10.1038/s41467-019-13767-1
73. Dual-Lifetime Referencing (t-DLR) Optical Fiber Fluorescent pH Sensor for Microenvironments W. Chen et al. https://doi.org/10.3390/s23218865
74. 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
75. 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
76. 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
77. Metabolic cost of calcification in bivalve larvae under experimental ocean acidification C. Frieder et al. https://doi.org/10.1093/icesjms/fsw213
78. 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
79. 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
80. Seagrass-driven changes in carbonate chemistry enhance oyster shell growth A. Ricart et al. https://doi.org/10.1007/s00442-021-04949-0
81. 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
82. 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
83. In vivo characterization of bivalve larval shells: a confocal Raman microscopy study K. Ramesh et al. https://doi.org/10.1098/rsif.2017.0723
84. 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
85. 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
86. Reconsidering the role of carbonate ion concentration in calcification by marine organisms L. Bach https://doi.org/10.5194/bg-12-4939-2015
87. Coupled ocean warming and acidification reduce shell integrity and bioenergetics in juvenile Mytilus coruscus B. Wang et al. https://doi.org/10.3354/meps15134
88. The Biological Crystals in Chamid Bivalve Shells: Diversity in Morphology and Crystal Arrangement Pattern S. Hoerl et al. https://doi.org/10.3390/cryst14070649
89. High Calcification Costs Limit Mussel Growth at Low Salinity T. Sanders et al. https://doi.org/10.3389/fmars.2018.00352
90. In situ recovery of bivalve shell characteristics after temporary exposure to elevated pCO2 J. Grear et al. https://doi.org/10.1002/lno.11456
91. 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
92. 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
93. 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
94. 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
95. 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
96. 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
97. 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
98. 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
99. 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
100. 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
101. 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
102. Ecotoxicological impacts of ocean alkalinity enhancement (OAE) on the European flat oyster Ostrea edulis: Insights from tissue metabolomics and metal analysis M. Rump et al. https://doi.org/10.1016/j.marenvres.2026.108439
103. Clumped isotopes in modern marine bivalves D. Huyghe et al. https://doi.org/10.1016/j.gca.2021.09.019
104. 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
105. 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