23 citations as recorded by crossref.

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7. Proceedings ISDSC5 F. Mienis et al. https://doi.org/10.1016/j.dsr2.2013.10.003
8. Physiological studies of the deep-water coral Madrepora oculata incubated at different temperatures and hydrostatic pressures B. Shillito et al. https://doi.org/10.1242/jeb.251200
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10. 3D-Representations for studying deep-sea coral habitats in the Lacaze-Duthiers Canyon, from geological settings to individual specimens M. Fabri et al. https://doi.org/10.1016/j.dsr.2022.103831
11. Thermal stress responses of the antipatharian Stichopathes sp. from the mesophotic reef of Mo'orea, French Polynesia M. Godefroid et al. https://doi.org/10.1016/j.scitotenv.2022.153094
12. pH up-regulation as a potential mechanism for the cold-water coral Lophelia pertusa to sustain growth in aragonite undersaturated conditions M. Wall et al. https://doi.org/10.5194/bg-12-6869-2015
13. Interactive Effects of Ocean Acidification and Warming on Growth, Fitness and Survival of the Cold-Water Coral Lophelia pertusa under Different Food Availabilities J. Büscher et al. https://doi.org/10.3389/fmars.2017.00101
14. Defying Dissolution: Discovery of Deep-Sea Scleractinian Coral Reefs in the North Pacific A. Baco et al. https://doi.org/10.1038/s41598-017-05492-w
15. Biomass mapping of fjordic cold-water coral reefs reveals distinct functional role of vertical wall habitat L. Greiffenhagen et al. https://doi.org/10.1016/j.dsr.2024.104350
16. Cold‐water coral ecosystems under future ocean change: Live coral performance vs. framework dissolution and bioerosion J. Büscher et al. https://doi.org/10.1002/lno.12217
17. Survival under conditions of variable food availability: Resource utilization and storage in the cold‐water coral Lophelia pertusa S. Maier et al. https://doi.org/10.1002/lno.11142
18. Skeletal growth and loss of the cold-water coral Lophelia pertusa from multiple environmental drivers in a year-long experiment K. Beck et al. https://doi.org/10.1525/elementa.2025.00037
19. Molecular mechanisms underlying the physiological responses of the cold-water coral Desmophyllum dianthus to ocean acidification M. Carreiro-Silva et al. https://doi.org/10.1007/s00338-014-1129-2
20. Effects of the sea lice chemotherapeutant, emamectin benzoate, on metabolism and behaviour of the sea-pen Pennatula phosphorea B. Taormina et al. https://doi.org/10.1016/j.marpolbul.2023.115903
21. Regulation of ion transport and energy metabolism enables certain coral genotypes to maintain calcification under experimental ocean acidification A. Glazier et al. https://doi.org/10.1111/mec.15439
22. Effects of elevated pCO2 and feeding on net calcification and energy budget of the Mediterranean cold-water coral Madrepora oculata C. Maier et al. https://doi.org/10.1242/jeb.127159
23. Natural hypoxic conditions do not affect the respiration rates of the cold-water coral Desmophyllum pertusum (Lophelia pertusa) living in the Angola margin (Southeastern Atlantic Ocean) A. Gori et al. https://doi.org/10.1016/j.dsr.2023.104052