CO2 and calcification processes in fish
暂无分享,去创建一个
[1] I. Ruiz-Jarabo,et al. Increased intestinal carbonate precipitate abundance in the sea bream (Sparus aurata L.) in response to ocean acidification , 2019, PloS one.
[2] G. Raby,et al. Long-term acclimation to near-future ocean acidification has negligible effects on energetic attributes in a juvenile coral reef fish , 2019, Oecologia.
[3] Blaine R. Roberts,et al. The inner ear proteome of fish , 2018, The FEBS journal.
[4] R. Hannigan,et al. Ocean acidification alters morphology of all otolith types in Clark’s anemonefish (Amphiprion clarkii) , 2018, PeerJ.
[5] G. Nilsson,et al. The physiology of behavioral impacts of high CO2 , 2019, Fish Physiology.
[6] C. Damsgaard,et al. Acid-base physiology and CO2 homeostasis: Regulation and compensation in response to elevated environmental CO2 , 2019, Fish Physiology.
[7] P. V. Skov. CO2 in aquaculture , 2019, Fish Physiology.
[8] C. Wood. Internal spatial and temporal CO2 dynamics: Fasting, feeding, drinking, and the alkaline tide , 2019, Fish Physiology.
[9] E. G. Xu,et al. Interrogation of the Gulf toadfish intestinal proteome response to hypersalinity exposure provides insights into osmoregulatory mechanisms and regulation of carbonate mineral precipitation. , 2018, Comparative biochemistry and physiology. Part D, Genomics & proteomics.
[10] G. Edgar,et al. Reef fish carbonate production assessments highlight regional variation in sedimentary significance , 2018, Geology.
[11] M. Grosell,et al. Comparison of the organic matrix found in intestinal CaCO3 precipitates produced by several marine teleost species. , 2018, Comparative biochemistry and physiology. Part A, Molecular & integrative physiology.
[12] C. Coll-Lladó,et al. Ocean acidification promotes otolith growth and calcite deposition in gilthead sea bream (Sparus aurata) larvae , 2018, Scientific Reports.
[13] S. Gregório,et al. Regulation of Bicarbonate Secretion in Marine Fish Intestine by the Calcium-Sensing Receptor , 2018, International journal of molecular sciences.
[14] Y. Takei,et al. Renoguanylin stimulates apical CFTR translocation and decreases HCO3− secretion through PKA activity in the Gulf toadfish (Opsanus beta) , 2018, Journal of Experimental Biology.
[15] P. Munday,et al. Diel CO2 cycles do not modify juvenile growth, survival and otolith development in two coral reef fish under ocean acidification , 2018 .
[16] M. Milazzo,et al. Ocean acidification does not impair predator recognition but increases juvenile growth in a temperate wrasse off CO2 seeps. , 2017, Marine environmental research.
[17] A. Oliveira,et al. Effects of high pCO2 on early life development of pelagic spawning marine fish , 2017 .
[18] B. Gillanders,et al. Elevated carbon dioxide and temperature affects otolith development, but not chemistry, in a diadromous fish , 2017 .
[19] A. Mirasole,et al. The influence of high pCO2 on otolith shape, chemical and carbon isotope composition of six coastal fish species in a Mediterranean shallow CO2 vent , 2017 .
[20] M. Grosell,et al. Fractionation of the Gulf toadfish intestinal precipitate organic matrix reveals potential functions of individual proteins. , 2017, Comparative biochemistry and physiology. Part A, Molecular & integrative physiology.
[21] A. Harborne,et al. Phase heterogeneity in carbonate production by marine fish influences their roles in sediment generation and the inorganic carbon cycle , 2017, Scientific Reports.
[22] W. Warren,et al. A proteinaceous organic matrix regulates carbonate mineral production in the marine teleost intestine , 2016, Scientific Reports.
[23] M. Grosell,et al. Elevated CO2 increases energetic cost and ion movement in the marine fish intestine , 2016, Scientific Reports.
[24] M. Grosell,et al. Changes to Intestinal Transport Physiology and Carbonate Production at Various CO2 Levels in a Marine Teleost, the Gulf Toadfish (Opsanus beta) , 2016, Physiological and Biochemical Zoology.
[25] David Schoppik,et al. Otolith size and the vestibulo-ocular reflex of larvae of white seabass Atractoscion nobilis at high pCO2 , 2016 .
[26] Y. Takei,et al. The role of the rectum in osmoregulation and the potential effect of renoguanylin on SLC26a6 transport activity in the Gulf toadfish (Opsanus beta). , 2016, American journal of physiology. Regulatory, integrative and comparative physiology.
[27] P. Falkowski,et al. Temporal and spatial expression patterns of biomineralization proteins during early development in the stony coral Pocillopora damicornis , 2016, Proceedings of the Royal Society B: Biological Sciences.
[28] Michael P Lesser,et al. Comparative genomics explains the evolutionary success of reef-forming corals , 2016, eLife.
[29] I. Nagelkerken,et al. Lost at sea: ocean acidification undermines larval fish orientation via altered hearing and marine soundscape modification , 2016, Biology Letters.
[30] S. Meseck,et al. Effect of ocean acidification on growth and otolith condition of juvenile scup, Stenotomus chrysops , 2015, Ecology and evolution.
[31] Y. Takei,et al. The differential role of renoguanylin in osmoregulation and apical Cl-/HCO3- exchange activity in the posterior intestine of the Gulf toadfish (Opsanus beta). , 2015, American journal of physiology. Regulatory, integrative and comparative physiology.
[32] J. Mu,et al. Effects of CO2-driven ocean acidification on early life stages of marine medaka (Oryzias melastigma) , 2015 .
[33] R. Jeffree,et al. Ocean acidification reshapes the otolith-body allometry of growth in juvenile sea bream , 2015 .
[34] M. Grosell,et al. Physiological impacts of elevated carbon dioxide and ocean acidification on fish. , 2014, American journal of physiology. Regulatory, integrative and comparative physiology.
[35] Y. Takei,et al. Guanylin peptides regulate electrolyte and fluid transport in the Gulf toadfish (Opsanus beta) posterior intestine. , 2014, American journal of physiology. Regulatory, integrative and comparative physiology.
[36] P. Pousão‐Ferreira,et al. Defective skeletogenesis and oversized otoliths in fish early stages in a changing ocean , 2014, Journal of Experimental Biology.
[37] C. Clemmesen,et al. Within- and transgenerational effects of ocean acidification on life history of marine three-spined stickleback (Gasterosteus aculeatus) , 2014 .
[38] D. Power,et al. Endocrine regulation of carbonate precipitate formation in marine fish intestine by stanniocalcin and PTHrP , 2014, Journal of Experimental Biology.
[39] H. Onken,et al. Osmoregulation and excretion. , 2014, Comprehensive Physiology.
[40] Jonathan M. Wilson,et al. Expression of Key Ion Transporters in the Gill and Esophageal-Gastrointestinal Tract of Euryhaline Mozambique Tilapia Oreochromis mossambicus Acclimated to Fresh Water, Seawater and Hypersaline Water , 2014, PloS one.
[41] S. Weiner,et al. Biogenic Fish-gut Calcium Carbonate is a Stable Amorphous Phase in the Gilt-head Seabream, Sparus aurata , 2013, Scientific Reports.
[42] R. Cowen,et al. Ocean acidification alters the otoliths of a pantropical fish species with implications for sensory function , 2013, Proceedings of the National Academy of Sciences.
[43] R. Cowen,et al. Response to ocean acidification in larvae of a large tropical marine fish, Rachycentron canadum , 2013, Global change biology.
[44] P. Falkowski,et al. Proteomic analysis of skeletal organic matrix from the stony coral Stylophora pistillata , 2013, Proceedings of the National Academy of Sciences.
[45] D. Power,et al. Adaptation to different salinities exposes functional specialization in the intestine of the sea bream (Sparus aurata L.) , 2013, Journal of Experimental Biology.
[46] Jessica A. Miller,et al. Resiliency of juvenile walleye pollock to projected levels of ocean acidification , 2012 .
[47] M. Salter,et al. Production of mud‐grade carbonates by marine fish: Crystalline products and their sedimentary significance , 2012 .
[48] Yan Wang,et al. Characterization of the Pearl Oyster (Pinctada martensii) Mantle Transcriptome Unravels Biomineralization Genes , 2012, Marine Biotechnology.
[49] M. Grosell,et al. Ocean Acidification Leads to Counterproductive Intestinal Base Loss in the Gulf Toadfish (Opsanus beta) , 2012, Physiological and Biochemical Zoology.
[50] M. Romero,et al. Euryhaline pufferfish NBCe1 differs from nonmarine species NBCe1 physiology. , 2012, American journal of physiology. Cell physiology.
[51] C. Wood,et al. Independence of net water flux from paracellular permeability in the intestine of Fundulus heteroclitus, a euryhaline teleost , 2012, Journal of Experimental Biology.
[52] S. Simpson,et al. Ocean acidification erodes crucial auditory behaviour in a marine fish , 2011, Biology Letters.
[53] A. Franke,et al. Effect of ocean acidification on early life stages of Atlantic herring (Clupea harengus L.) , 2011 .
[54] S. Guffey,et al. Regulation of apical H⁺-ATPase activity and intestinal HCO₃⁻ secretion in marine fish osmoregulation. , 2011, American journal of physiology. Regulatory, integrative and comparative physiology.
[55] F. Millero,et al. The solubility of fish‐produced high magnesium calcite in seawater , 2011 .
[56] S. Perry,et al. Compensatory regulation of acid–base balance during salinity transfer in rainbow trout (Oncorhynchus mykiss) , 2011, Journal of Comparative Physiology B.
[57] M. Grosell. Intestinal Anion Exchange in Marine Teleosts Is Involved in Osmoregulation and Contributes to the Oceanic Inorganic Carbon Cycle , 2022 .
[58] P. Munday,et al. Effect of ocean acidification on otolith development in larvae of a tropical marine fish , 2011 .
[59] M. McDonald,et al. Concentration of MgSO4 in the intestinal lumen of Opsanus beta limits osmoregulation in response to acute hypersalinity stress. , 2011, American journal of physiology. Regulatory, integrative and comparative physiology.
[60] M. Radmacher,et al. Modification of CaCO3 precipitation rates by water-soluble nacre proteins , 2011 .
[61] Howard L. Jelks,et al. Fish as major carbonate mud producers and missing components of the tropical carbonate factory , 2011, Proceedings of the National Academy of Sciences.
[62] P. Munday,et al. Ocean acidification does not affect the early life history development of a tropical marine fish. , 2011 .
[63] S. Perry,et al. Acid–base regulation in the plainfin midshipman (Porichthys notatus): an aglomerular marine teleost , 2010, Journal of Comparative Physiology B.
[64] M. Beltramini,et al. Cytosolic carbonic anhydrase in the Gulf toadfish is important for tolerance to hypersalinity. , 2010, Comparative biochemistry and physiology. Part A, Molecular & integrative physiology.
[65] M. Tresguerres,et al. Modulation of NaCl absorption by [HCO(3)(-)] in the marine teleost intestine is mediated by soluble adenylyl cyclase. , 2010, American journal of physiology. Regulatory, integrative and comparative physiology.
[66] R. Wilson,et al. Ca2+-driven intestinal HCO(3)(-) secretion and CaCO3 precipitation in the European flounder in vivo: influences on acid-base regulation and blood gas transport. , 2010, American journal of physiology. Regulatory, integrative and comparative physiology.
[67] E. Mager,et al. Basolateral NBCe1 plays a rate-limiting role in transepithelial intestinal HCO3– secretion, contributing to marine fish osmoregulation , 2010, Journal of Experimental Biology.
[68] M. Grosell. The role of the gastrointestinal tract in salt and water balance , 2010 .
[69] J. Taylor,et al. The intestinal response to feeding in seawater gulf toadfish, Opsanus beta, includes elevated base secretion and increased epithelial oxygen consumption , 2009, Journal of Experimental Biology.
[70] S. Perry,et al. The involvement of H+-ATPase and carbonic anhydrase in intestinal HCO3– secretion in seawater-acclimated rainbow trout , 2009, Journal of Experimental Biology.
[71] E. Mager,et al. High rates of HCO3– secretion and Cl– absorption against adverse gradients in the marine teleost intestine: the involvement of an electrogenic anion exchanger and H+-pump metabolon? , 2009, Journal of Experimental Biology.
[72] R. Asch,et al. Elevated CO2 Enhances Otolith Growth in Young Fish , 2009, Science.
[73] V. Christensen,et al. Contribution of Fish to the Marine Inorganic Carbon Cycle , 2009, Science.
[74] M. Grosell,et al. Effects of salinity on intestinal bicarbonate secretion and compensatory regulation of acid–base balance in Opsanus beta , 2008, Journal of Experimental Biology.
[75] F. Marin,et al. Unusually Acidic Proteins in Biomineralization , 2008 .
[76] A. Kato,et al. Identification of intestinal bicarbonate transporters involved in formation of carbonate precipitates to stimulate water absorption in marine teleost fish , 2008, American journal of physiology. Regulatory, integrative and comparative physiology.
[77] Y. Takei,et al. Regulation of Ion Transport in Eel Intestine by the Homologous Guanylin Family of Peptides , 2007, Zoological science.
[78] S. Perry,et al. Intestinal carbonic anhydrase, bicarbonate, and proton carriers play a role in the acclimation of rainbow trout to seawater. , 2007, American journal of physiology. Regulatory, integrative and comparative physiology.
[79] M. Grosell,et al. Intestinal anion exchange in teleost water balance. , 2007, Comparative biochemistry and physiology. Part A, Molecular & integrative physiology.
[80] M. Fritz,et al. Perlinhibin, a cysteine-, histidine-, and arginine-rich miniprotein from abalone (Haliotis laevigata) nacre, inhibits in vitro calcium carbonate crystallization. , 2007, Biophysical journal.
[81] Y. Takei,et al. The intestinal guanylin system and seawater adaptation in eels. , 2007, General and comparative endocrinology.
[82] G. Nehrke,et al. Dissolution of Calcidiscus leptoporus coccoliths in copepod guts?- A morphological study , 2007 .
[83] H. Nagasawa,et al. Localization and diurnal variations of carbonic anhydrase mRNA expression in the inner ear of the rainbow trout Oncorhynchus mykiss. , 2006, Comparative biochemistry and physiology. Part B, Biochemistry & molecular biology.
[84] M. Grosell. Intestinal anion exchange in marine fish osmoregulation , 2006, Journal of Experimental Biology.
[85] M. Grosell,et al. Ouabain-sensitive bicarbonate secretion and acid absorption by the marine teleost fish intestine play a role in osmoregulation. , 2006, American journal of physiology. Regulatory, integrative and comparative physiology.
[86] H. Nagasawa,et al. Diel changes in endolymph aragonite saturation rate and mRNA expression of otolith matrix proteins in the trout otolith organ , 2005 .
[87] F. Jensen,et al. Bicarbonate secretion plays a role in chloride and water absorption of the European flounder intestine. , 2005, American journal of physiology. Regulatory, integrative and comparative physiology.
[88] W. Marshall. Ion transport, osmoregulation, and acid-base balance , 2005 .
[89] M. Grosell. 6 Ion Transport, Osmoregulation, and Acid-Base Balance , 2005 .
[90] Richard A. Feely,et al. Impact of Anthropogenic CO2 on the CaCO3 System in the Oceans , 2004, Science.
[91] F. Jensen,et al. Intestinal HCO3− secretion in marine teleost fish: evidence for an apical rather than a basolateral Cl−/HCO3− exchanger , 2001, Fish Physiology and Biochemistry.
[92] M. Ando,et al. Characterization of esophageal desalination in the seawater eel,Anguilla japonica , 2004, Journal of Comparative Physiology B.
[93] R. Wilson,et al. Intestinal bicarbonate secretion in marine teleost fish-source of bicarbonate, pH sensitivity, and consequences for whole animal acid-base and calcium homeostasis. , 2003, Biochimica et biophysica acta.
[94] Jonathan M. Wilson,et al. Intestinal bicarbonate secretion by marine teleost fish--why and how? , 2002, Biochimica et biophysica acta.
[95] G. Boeuf,et al. Otolith growth in trout Oncorhynchus mykiss: supply of Ca2+ and Sr2+ to the saccular endolymph. , 2002, The Journal of experimental biology.
[96] Dieter Wolf-Gladrow,et al. Modeling the dissolution of settling CaCO3 in the ocean , 2002 .
[97] G. Boeuf,et al. Biochemical Relationships Between Endolymph and Otolith Matrix in the Trout (Oncorhynchus mykiss) and Turbot (Psetta maxima) , 2001, Calcified Tissue International.
[98] H. Tohse,et al. Effects of enzyme and anion transport inhibitors on in vitro incorporation of inorganic carbon and calcium into endolymph and otoliths in salmon Oncorhynchus masou. , 2001, Comparative biochemistry and physiology. Part A, Molecular & integrative physiology.
[99] G. Boeuf,et al. Chemical composition of saccular endolymph and otolith in fish inner ear: lack of spatial uniformity. , 1999, American journal of physiology. Regulatory, integrative and comparative physiology.
[100] R. Wilson. Regulation of Tissue pH in Plants and Animals: A novel role for the gut of seawater teleosts in acid–base balance , 1999 .
[101] G. Boeuf,et al. Ionic composition of endolymph in teleosts: origin and importance of endolymph alkalinity. , 1997, The Journal of experimental biology.
[102] G. Boeuf,et al. Distribution of ionocytes in the saccular epithelium of the inner ear of two teleosts (Oncorhynchus mykiss and Scophthalmus maximus) , 1997, Cell and Tissue Research.
[103] Gilmour,et al. Intestinal base excretion in the seawater-adapted rainbow trout: a role in acid-base balance? , 1996, The Journal of experimental biology.
[104] Ando,et al. Intestinal Na+ and Cl- levels control drinking behavior in the seawater-adapted eel Anguilla japonica , 1996, The Journal of experimental biology.
[105] P. Walsh,et al. Carbonate deposits in marine fish intestines: A new source of biomineralization , 1991 .
[106] Y. Mugiya. Effects of calmodulin inhibitors and other metabolic modulators on In Vitro otolith formation in the rainbow trout, Salmo gairdnerii , 1986 .
[107] J. Renfro,et al. Esophageal desalination of seawater in flounder: role of active sodium transport. , 1983, The American journal of physiology.
[108] T. Hirano,et al. Eel esophagus as an osmoregulatory organ. , 1976, Proceedings of the National Academy of Sciences of the United States of America.
[109] O. Lowenstein. 7 The Labyrinth , 1971 .
[110] M. Gordon,et al. The role of the intestine in salinity adaptation of the rainbow trout, Salmo gairdneri , 1969 .
[111] R. Haedrich,et al. Molecular structure and composition of fish otoliths , 1969 .
[112] Walter Schellenberg,et al. The Labyrinth , 2020, The Networked School Leader.
[113] Homer W. Smith. THE ABSORPTION AND EXCRETION OF WATER AND SALTS BY MARINE TELEOSTS , 1930 .