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Iran J Fish Sci 9(1):33–48\nCampbell PM, Pottinger TG, Sumpter JP (1992) Stress reduces the quality of gametes produced by rainbow trout. Biol Reprod 47:1140–1150\nCosson J (2004) The ionic and osmotic factors controlling motility of fish spermatozoa. Aquac Int 12:69–85\nCraik JCA, Harvey SM (1984) Egg quality in rainbow trout: the relation between egg viability, selected aspects of egg composition, and time of stripping. Aquaculture 40:115–134\nde Gaudemar B, Beall E (1998) Effects of overripening on spawning behaviour andreproductive success of Atlantic salmon females spawning ina controlled flow channel. J Fish Biol 53:434–446\nDuan Q, Mai K, Zhong H, Si L, Wang X (2001) Studies on the nutrition of the large yellow croaker, Pseudosciaena crocea R. I: growth response to graded levels of dietary protein and lipid. Aquac Res 32:46–52\nHélène R, Nathalie G, Charles P, Emilie B, Julien B, Bernard J (2004) Post-ovulatory ageing and egg quality: a proteomic analysis of rainbow trout coelomic fluid. Reprod Biol Endocrinol 2:26\nJian S (1985) Training manual integrated fish farming in china. FAO. http:\u002F\u002Fwww.fao.org\u002Fdocrep\u002Ffield\u002F003\u002Fac233e\u002FAC233E00.htm#TOC. Accessed 4 Jan 2017\nLahnsteiner F (2000) Morphological, physiological and biochemical parameters characterizing the over-ripening of rainbow trout eggs. Fish Physiol Biochem 23:107–118\nLiu X, Zhao G, Wang Z, Mingyi C, Hua Y, Qiurong W (2012) Parentage assignment and parental contribution analysis in large yellow croaker Larimichthys crocea using microsatellite markers. Curr Zool 58(2):244–249\nNovelo ND, Tiersch T (2016) Development and evaluation of an ultrasound imaging reproductive index based on the ovarian cycle of channel catfish, Ictalurus punctatus. J World Aquac Soc 47(4):526–537\nRasines I, Gómez M, Martín I, Rodríguez C, Mañanós E, Chereguini O (2012) Artificial fertilization of Senegalese sole (Solea senegalensis): hormone therapy administration methods, timing of ovulation and viability of eggs retained in the ovarian cavity. Aquaculture 326–329:129–135\nRottmann JVS, Chapman FA (1991) Techniques for taking and fertilizing the spawn of fish. SRAC 426:1–8\nSchulz DR, Perez N, Tan CK, Mendez AJ, Capo TR, Snodgrass D, Prince ED, Serafy JE (2005) Concurrent levels of 11-ketotestosterone in fish surface mucus, muscle tissue and blood. J Appl Ichthyol 21:394–398\nSoso AB, Barcellos LJG, Ranzani-Paiva MJ (2008) The effects of stressful broodstock handling on hormonal profiles and reproductive performance of Rhamdia quelen (Quoy and Gaimard) females. J World Aquacult Soc 39:835–841\nSpringate JRC, Bromage NR, Elliott JAK, Hudson DL (1984) The timing of ovulation and stripping and their effects on the rates of fertilization and survival to eying, hatch and swim-up in the rainbow trout (Salmo gairdneri R.). Aquaculture 43:313–322\nTang T (2016) The foundation of science and technological innovation alliance for national large yellow croaker industry. China Fisheries News (in Chinese)\nZakęś Z, Demska-Zakęś K (2005) Artificial spawning of pikeperch (Sander lucioperca L.) stimulated with human chorionic gonadotropin (hCG) and mammalian GnRH analogue with a dopamine inhibitor. Arch Pol Fish 13:63–75\nZheng C, Wu X, Jiang H (2006) Broodstock management and artificial fertilization technologyresearch in the large yellow croaker (Pseudosciaena crocea). China Fish 7:86–87",{"EN":121},"Large yellow croaker is an important marine aquaculture species in China. The aim was to determine an appropriate protocol of artificial fertilization for family construction in the breeding programme based on two trials. In trial 1, luteinizing hormone-releasing hormone A3 (LHRHA3) was injected once, with a dosage of 2 μg\u002Fkg for females and 1 μg\u002Fkg for males. The latency time was in the range of 30–34 h. The maturation stage was checked by extracting a few eggs with a Pasteur pipette. The fertilization rate and hatching rate were 27 and 52%, respectively. The percentage of females with spawning difficulties was 30%. In trial 2, the females were injected LHRHA3 twice: with a first dose of 0.8 μg\u002Fkg and a second dose of 2 μg\u002Fkg, at an interval of 10 h, whereas the males were still injected once. The latency time was in the range of 29.5–35 h, determined by only observing courtship behaviour of males. 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M (2016) Past, present, and future roles of small cladoceran Bosmina longirostris (O. F. Müller, 1785) in aquatic ecosystems. Hydrobiologia 767:1–11\nArruda JA, Marzolf GR, Faulk RT (1983) The role of suspended sediments in the nutrition of zooplankton in turbid reservoirs. Ecology 64:1225–1235\nBattarbee RW (1999) The importance of paleolimnology to lake restoration. Hydrobiologia 395(396):149–159\nBelyaeva M, Deneke R (2007) Colonization of acidic mining lakes: Chydorus sphaericus and other Cladocera within a dynamic horizontal pH gradient (pH 3 − 7) in lake Senftenberger See (Germany). Hydrobiologia 594:97–108\nBelyaeva M, Taylor DJ (2009) Cryptic species within the Chydorus sphaericus species complex (Crustacea: Cladocera) revealed by molecular markers and sexual stage morphology. Mol Phylogenet Evol 50:534–546\nBennett K (1996) Determination of the number of zones in a biostratigraphical sequence. New Phytol 132:155–170\nBłędzki LA, Rybak JI (2016) Freshwater crustacean zooplankton of Europe. Springer, Swizerland\nBossuyt BTA, Janssen CR (2005) Copper toxicity to different field-collected cladoceran species: intra- and inter-species sensitivity. Environ Pollut 136:145–154\nBourg ACM, Loch JPG (1995) Mobilization of heavy metals as affected by pH and redox conditions. In: Salomons W, Stigliani WM (eds) Biogeodynamics of pollutants in soils and sediments. Environmental science. Springer, Berlin, pp 87–102\nBownik A (2017) Daphnia swimming behavior as a biomarker in toxicity assessment: a review. Sci Total Environ 601–602:194–205\nBozelli RL (1996) The influence of bauxite tailings on the cladoceran populations of Lake Batata, Amazonia, Brazil. Int Rev Hydrobiol 81:621–634\nBradbury JP, Megarad RO (1972) Stratigraphic record of pollution in Shagawa Lake, Northeastern Minnesota. Geol Soc Am Bull 83:2639–2648\nBrooks JL, Dodson SI (1965) Predation, body size and composition of plankton. Science 150:28–35\nCain DJ, Luoma SN, Carter JL, Fend SV (1992) Aquatic insects as bioindicators of trace element contamination in cobble-bottom rivers and streams. Can J Fish Aquat Sci 49:2141–5154\nCamargo JA, Alonso A, Salamanca A (2005) Nitrate toxicity to aquatic animals: a review with new data for freshwater invertebrates. Chemosphere 58:1255–1267\nCanadian Government (2002) Metal mining effluent regulations. SOR\u002F2002-222\nCanton SP, Ward JV (1981) Benthos and zooplankton of coal strip mine ponds in the mountains of northwestern Colorado, U.S.A. Hydrobiologia 85:23–31\nChen G, Shi H, Tao J, Chen L, Liu Y, Lei G, Liu X, Smol P (2016) Industrial arsenic contamination causes catastrophic changes in freshwater ecosystem. Sci Rep 5:17419. https:\u002F\u002Fdoi.org\u002F10.1038\u002Fsrep17419\nClarke KR (1993) Non-parametric multivariate analysis of changes in community structure. Aust J Ecol 18:117–143\nCoard MA, Cousen SM, Cuttler AH, Dean HJ, Dearing JA, Eglinton TI, Greaves AM, Lacey KP, O’Sullivan PE, Pickering DA, Rhead MM, Rodwell JK, Simola H (1983) Paleolimnological studies of annually-laminated sediments in Loe Pool, Cornwall, U.K. Hydrobiologia 103:185–191\nCuker BE (1987) Field experiment on the influences of suspended clay and P on the plankton of a small lake. Limnol Oceanogr 32:840–847\nDekker T, Greve GD, Ter Laak TL, Boivin ME, Veuger B, Gortzak G, Dumfries S, Lücker SMG, Kraak MHS, Admiraal W, van der Geest HG (2005) Development and application of a sediment toxicity test using the benthic cladoceran Chydorus sphaericus. Environ Pollut 140:231–238\nDoig LE, Schiffer ST, Liber K (2015) Reconstructing the ecological impacts of eight decades of mining, metallurgical, and municipal activities on a small boreal lake in Norther Canada. Integr Environ Assess Manag 11:490–501\nDraves JF, Fox MC (1998) Effects of a mine tailings spill on feeding and metal concentrations in juvenile perch (Perca fluviatilis). Environ Toxicol Chem 17:1626–1632\nDumont HJ (1989) The non-marine Cladocera in Belgium. In: Wouters K, Baert, L (eds) Proceedings of the symposium “Invertebrates of Belgium”. Brussel, 25–26 November 1988, pp 137–142\nECOTOX (2017) The ecotoxicology database. https:\u002F\u002Fcfpub.epa.gov\u002Fecotox\u002Fecotox_home.cfm. Accessed 17 May 2017\nEl-Bassat RA, Taylor WD (2007) The zooplankton community of Lake Abo Zaabal, a newly-formed mining lake in Cairo, Egypt. Afr J Aquat Sci 32:185–192\nElphick JR, Davies M, Gilron G, Canaria EC, Lo B, Bailey HC (2011) An aquatic toxicological evaluation of sulfate: the case for considering hardness as a modifying factor in setting water quality guidelines. Environ Toxicol Chem 30:247–257\nEuropean Union (2000) Directive 2000\u002F60\u002FEC of the European Parliament and of the Council of 23 October 2000 establishing a framework for community action in the field of water policy. Off J Eur Communities L327:1–72\nFerrari CR, Wisniewski MJ, Roque CV, Ronque LB, Campos MB, Rodgher S, Nascimento MRL, de Azevedo H (2009) Preliminary assessment of the zooplankton community composition in a region under the influence of a uranium mine (Caldas, southeastern Brazil). International Nuclear Atlantic Conference—INAC 2009. Rio de Janeiro, RJ, Brazil, September 27 to October 2, 2009 (ISBN 978-85-99141-03-8)\nFerrari CR, de Azevedo H, Wisniewski MJS, Roddgher S, Roque CV, Nascimento MRL (2015) An overview of an acidic uranium mine pit lake (Caldas, Brazil): composition of the zooplankton community and limnochemical aspects. Mine Water Environ 34:343–351\nFerrari CR, de Azevedo H, Nascimento F, Rodgher S, Almeida T, Bruschi AL, Nascimento MRL, Bonifacio RL (2017) Effects of the discharge of uranium mining effluents on the water quality of the reservoir: an integrative chemical and ecotoxicological assessment. Sci Rep 7:13919. https:\u002F\u002Fdoi.org\u002F10.1038\u002Fs41598-017-14100-w\nGarrido AV, Bozelli RL, De Esteves FA, Alves LS (2003) Long-term patterns of the planktonic cladoceran community of Batata Lake, Amazonia, Brazil. Acta Limnol Bras 15:41–53\nGriffiths K, Thienpont J, Jeziorski A, Smol JP (2018) The impact of Ca-rich diamond mining effluent on downstream communities in softwater lakes of the Northwest Territories, Canada. Can J Fish Aquat Sci. https:\u002F\u002Fdoi.org\u002F10.1139\u002Fcjfas-2017-0469\nHart RC (1987) Population dynamics and production of five crustacean zooplankton in a subtropical reservoir during years of contrasting turbidity. Freshw Biol 18:287–318\nHarwell MA, Harwell CC, Weinstein DA, Kelly JR (1987) Anthropogenic stresses on ecosystems: issues and indicators of response and recovery. ERC-153. Ecosystems Research Center, Ithaca\nHeine-Fuster I, Vega-Retter C, Sabat P, Ramos-Jiliberto R (2010) Osmoregulatory and demographic responses to salinity of the exotic cladoceran Daphnia exilis. J Plankton Res 32:1405–1411\nHolopainen IJ, Holopainen A-L, Huitu E, Rahkola-Sorsa M, Zingel P (2008) The pelagic food web in forest lakes affected by alkaline mining waste in NW Russia. Est J Ecol 57:214–228\nHudson-Edwards KA, Dold B (2015) Mine waste characterization, management and remediation. Minerals 5:82–85\nJäger IS, Hölker F, Flöder S, Walz N (2011) Impact of Chaoborus flavicans on the zooplankton in a mesotrophic lake—a three year study. Internat Rev Hydrobiol 96:191–208\nJeppesen E, Nõges P, Davidson T, Haberman J, Nõges T, Blank K, Lauridsen T, Søndergaard M, Sayer C, Laugaste R, Johansson L, Bjerring R, Amsinck S (2011) Zooplankton as indicators in lakes: a scientific—based plea for including zooplankton in the ecological quality assessment of lakes according to the European Water Framework Directive (WFD). Hydrobiologia 676:279–297\nKerfoot WC, Robbins JA, Weider LJ (1999) A new approach to historical reconstruction: combining descriptive and experimental paleolimnology. Limnol Oceanogr 44:1232–1247\nKirk KL, Gilbert JJ (1990) Suspended clay and the population dynamics of planktonic rotifers and cladocerans. Ecology 71:1741–1755\nKlapper H, Schultze M (1995) Geogenically acidified mining lakes—living conditions and possibilities of restoration. Int Rev Hydrobiol 80:639–653\nKoivisto S, Ketola M (1995) Effects of copper on life-history traits of Daphnia pulex and Bosmina longirostris. Aquat Toxicol 32:255–269\nKoivisto S, Ketola M, Walls M (1992) Comparison of 5 cladoceran species in short- and long-term copper exposure. Hydrobiologia 248:125–136\nKorhola A, Rautio M (2001) Cladocera and other Branchiopod crustaceans. In: Smol JP, Birks HJB, Last WM (eds) Tracking environmental change using lake sediments, vol 4. Zoological indicators. Kluwer Academic Publishers, Dordrecht, pp 5–41\nKorosi JB, Kurek J, Smol JP (2013) A review on utilizing Bosmina size structure archieved in lake sediments to infer historic shifts in predation regimes. J Plankton Res 53:444–460\nKozlova T, Wood CM, McGeer JC (2008) The effect of water chemistry on the acute toxicity of nickel to cladoceran Daphnia pulex and the development of a biotic ligand model. Aquat Toxicol 91:221–228\nKurek J, Kirk JL, Muir DCG, Wang X, Evans MS, Smol JP (2012) Legacy of a half century of Athabasca oil and development recorded by lake ecosystems. Proc Natl Acad Sci USA 110:1761–1766\nLabaj AL, Jeziorski A, Kurek J, Smol JP (2014) Long-term trends in Cladoceran assemblages related to acidification and subsequent liming of Middle Lake (Sudbury Canada). Water Air Soil Pollut 225:1868. https:\u002F\u002Fdoi.org\u002F10.1007\u002Fs11270-014-1868-2\nLabaj AL, Kurek J, Jeziorski A, Smol JP (2015) Elevated metal concentrations inhibit biological recovery of Cladocera in previously acidified boreal lakes. Freshw Biol 60:347–359\nLampert W (2011) Daphnia: development of a model organism in ecology and evolution. Excellence in ecology, book 21. International Ecology Institute, Oldendorf\nLeppänen J, Siitonen S, Weckström J (2016) The stability of cladoceran communities in sub-arctic NW Finnish Lapland lakes. Polar Biol 40:2211–2223\nLeppänen J, Weckström J, Korhola A (2017a) Paleolimnological fingerprinting of the impact of acid mine drainage after 50 years of chronic pollution in a southern Finnish lake. Water Soil Air Pollut 228:227. https:\u002F\u002Fdoi.org\u002F10.1007\u002Fs11270-017-3417-2\nLeppänen J, Weckström J, Korhola A (2017b) Mining pollution triggered a regime shift in cladoceran community of Lake Kirkkojärvi. J Paleolimnol, S Finland. https:\u002F\u002Fdoi.org\u002F10.1007\u002Fs10933-018-0030-3\nLeppänen J, Weckström J, Korhola A (2017c) Multiple mining impacts induce widespread changes in ecosystem dynamics in a boreal lake. Sci Rep 7:10581. https:\u002F\u002Fdoi.org\u002F10.1038\u002Fs41598-017-11421-8\nLindenmayer DB, Likens GE (2009) Adaptive monitoring: a new paradigm for long-term research and monitoring. Trends Ecol Evol 24:482–486\nLopes I, Goncalves F, Soares AMVM, Ribeiro R (1999) Discriminating the ecotoxicity due to metals and to low pH in acid mine drainage. Ecotox Environ Safe 44:207–214\nLundstedt L, Brett MT (1991) Differential growth rates of three cladoceran species in response to mono- and mixed-algal cultures. Limnol Oceanogr 36:159–165\nMaia-Barbosa PM, Bozelli RR (2005) Length-weight relationships for five cladoceran species in an Amazonian lake. Braz Arch Biol Technol 48:303–308\nMarkert BA, Breure AM, Zechmeister HG (2003) Definitions, strategies and principles for bioindication\u002Fbiomonitoring. In: Markert BA, Breure AM, Zechmeister HG (eds) Bioindicators & biomonitors. Principles, concepts and applications. Trace metals and other contaminants in the environment 6. Elsevier, Kidlington, pp 3–39\nMcCabe GD, O’Brien WJ (1983) The effects of suspended silt on feeding and reproduction of Daphnia pulex. Am Midl Nat 110:324–337\nMelville GE (1995) Changes in pelagic crustacean zooplankton of high-boreal Island Lake, Saskatchewan, associated with uranium mining. Environ Monit Assess 34:45–58\nMiller GC, Lyons WB, Davis A (1996) Understanding the water quality of pit lakes. Environ Sci Technol 30:118A–123A\nMolenda T (2014) Impact of saline mine water: development of a meromictic reservoir in Poland. Mine Water Environ 33:327–334\nMoreira FWA, Leite MGP, Fujaco MAG, Mendoca FPC, Campos LP, Eskinazi-Sankt’Anna EM (2016) Assessing the impacts of mining activities on zooplankton functional diversity. Acta Limnol Bras. https:\u002F\u002Fdoi.org\u002F10.1590\u002FS2179-975X0816\nMoser M, Weisse T (2011) The most acidified Austrian lake in comparison to a neutralized mining lake. Limnologica 41:303–315\nNevalainen L, Luoto TP (2013) Limnological deterioration forces community and phenotypic changes in Cladocera: tracking eutrophication of Mallusjärvi, a lake in southern Finland. Boreal Env Res 18:209–222\nNixdorf B, Mischke U, Leßmann D (1998) Chrysophytes and chlamydomonads: pioneer colonists in extremely acidic mining lakes (pH \u003C 3) in Lusatia (Germany). Hydrobiologia 369(370):315–327\nNiyogi S, Wood CM (2004) Biotic ligand model, a flexible tool for developing site-specific water quality guidelines for metals. Environ Sci Technol 38:6177–6192\nNordstrom DK (2011) Mine waters: acidic to circumneutral. Elements 7:393–398\nPersoone G, Baudo R, Cotman M, Blaise C, Thompson KCL, Moreira-Santos M, Vollat B, Törökne A, Han T (2009) Review on the acute Daphnia magna toxicity test—evaluation of the sensitivity and the precision of assays performed with organisms from laboratory cultures or hatched from dormant eggs. Knowl Manag Aquat Ecosyst 393:1. https:\u002F\u002Fdoi.org\u002F10.1051\u002Fkmae\u002F2009012\nReichl C, Schatz M, Zsak G (2016) World mining data. Volume 31. Minerals Production. International organizing committee for the world mining congresses. 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J Paleolimnol 41:243–252\nSchultze M, Pokrandt K-H, Hille W (2010) Pit lakes of the Central German lignite mining district: creation, morphometry and water quality aspects. Limnologica 40:148–155\nSchultze M, Boehrer B, Wendt-Potthoff K, Sánchez-España J, Castendyk D (2017) Meromictic pit lakes: case studies from Spain, Germany and Canada and general aspects of management and modelling. In: Gulati RD, Zadereev ES, Degermendzhi AG (eds) Ecology of meromictic lakes. Springer, Berlin, pp 235–275\nSienkiewicz E, Gąsiorowski M (2016) The evolution of a mining lake-From acidity to natural neutralization. Sci Total Environ 557–558:343–354\nSmirnov N (2017) Physiology of the Cladocera. Elsevier Academic Press, London\nSmol JP (1992) Paleolimnology: an important tool for effective ecosystem management. J Aquat Ecosyst Health 1:49–58\nSofyan A, Shaw JR, Birge WJ (2009) Metal trophic transfer from algae to cladocerans and the relative importance of dietary metal exposure. 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Anal Chim Acta 606:135–150",{"EN":229},"Mine-fed waters have been rigorously studied, but most of the ecological research on mine water has been conducted in riverine systems. Lakes, however, are known to recover from pollution more slowly than riverine systems and, thus, the impacts of mine water on lakes are equally interesting. One of the most important biological components in lakes are the Cladocera, an order of crustacean zooplankton. Cladocerans are regarded as excellent indicators of environmental change and, for example, genus Daphnia is one of the most used test organisms in ecotoxicology. While in vitro tests regarding pollutants and cladocerans have been reviewed multiple times, the literature regarding the community level responses to mine pollution in natural settings is still to be better explored. The main aim of this paper is to screen and compile the current literature related to cladoceran communities and mine-induced water pollution. In addition, the applicability of cladocerans as a bioindicators group in mine water studies will be explored. This review shows that cladocerans have been studied in many cases of mining related pollution and most of the research has been conducted in North America, central Europe and Brazil. Acidity, turbidity and metals pollution are nearly equally important in shaping cladoceran communities in mining impacted lakes. The most tolerant taxa to mining pollution are Bosmina spp. and Chydorus sphaericus. The group clearly has potential as community level bioindicator\u002Fbiomonitor in mining pollution studies, but challenges remain. Namely, the lack of data regarding the most sensitive taxa is a major problem when indicator value of any single species is assessed.",{"EN":231},"An overview of Cladoceran studies conducted in mine water impacted lakes",{"VOID":233},"10.1007\u002Fs40071-018-0204-7","VERIFIED","Auto Verify","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002Fs40071-018-0204-7",[238],{"id":239,"sortIndex":23,"researcher":22,"roles":240,"affiliations":241,"properties":250},"70eeea03-d088-44e1-9335-1ea6bd8e7231",[132],[242],{"id":22,"sortIndex":23,"affiliation":243,"properties":22},{"id":244,"createTime":245,"updateTime":245,"relativeEntities":246,"slug":22,"properties":247,"entityType":43,"verifyStatus":21,"verifyTime":22,"verifyNote":22,"syncStatus":21,"languages":22,"translateLanguages":22,"viewCount":23},"821a6cba-7e60-48ea-a190-a027912179e1","2024-01-26T07:24:36.107+00:00",[],{"title":248},{"VI":249},"Environmental Change Research Unit (ECRU) and Helsinki Institute of Sustainability Science, Faculty of Biological and Environmental Sciences, University of Helsinki, Helsinki, Finland",{"title":251},{"VI":252},"Jaakko Johannes Leppänen",{"url":236,"publisher":254,"properties":283},{"id":6,"createTime":7,"updateTime":8,"relativeEntities":255,"slug":10,"properties":256,"entityType":20,"verifyStatus":21,"verifyTime":22,"verifyNote":22,"syncStatus":21,"languages":22,"translateLanguages":22,"viewCount":23,"subjectFields":261,"manageAffiliations":262,"indexDatabases":263,"url":22,"thumbnailPath":22,"statistic":278,"gsStatistic":22,"type":108,"analyzePriority":22},[],{"issn":257,"eissn":258,"title":259,"url":260},{"VOID":13},{"VOID":15},{"EN":17},{"VOID":19},[],[],[264,271],{"id":58,"indexDatabase":265,"url":22,"indexYears":22,"academicFieldIds":270,"indexDatabaseRanking":22},{"id":60,"createTime":61,"updateTime":62,"relativeEntities":266,"label":267,"description":268,"key":69,"publicationTags":269,"standard":22},[],{"EN":65,"VI":65},{"VI":67,"EN":68},[71,72],[74],{"id":76,"indexDatabase":272,"url":89,"indexYears":90,"academicFieldIds":277,"indexDatabaseRanking":93},{"id":78,"createTime":79,"updateTime":80,"relativeEntities":273,"label":274,"description":275,"key":86,"publicationTags":276,"standard":22},[],{"EN":83,"VI":83},{"EN":83,"VI":85},[88],[92],{"impactFactor":23,"impactFactorByYear":279,"i10Index":23,"i10IndexLast5Year":23,"totalPublication":96,"totalPublicationByYear":280,"totalCitation":23,"totalCitationByYear":281,"totalCitationPerPublication":23,"totalCitationPerPublicationByYear":282,"hindexLast5Year":23,"hindex":23},{},{"2012":98,"2013":99,"2014":100,"2015":101,"2016":102,"2017":103,"2018":104,"2019":105},{},{},{"volume":284,"pages":286},{"VOID":285},"10",{"VOID":287},"207-221","2018-08-23",2018,{"id":291,"createTime":292,"updateTime":293,"relativeEntities":294,"slug":295,"properties":296,"entityType":126,"verifyStatus":21,"verifyTime":22,"verifyNote":22,"syncStatus":21,"languages":22,"translateLanguages":22,"viewCount":23,"primaryUrl":307,"fullTextUrl":22,"authors":308,"publicationType":180,"publisherRelationship":519,"citationCount":464,"citationInfo":554,"publishDate":557,"publishYear":555,"citationAnalyzeStatus":558,"lastCitationAnalyze":293,"indexDatabases":22,"openAccess":22,"references":22,"isForceReanalyzing":218},"41548869-a6dd-45c7-bd70-c18d25925f4f","2024-01-24T22:44:18.852+00:00","2024-12-25T23:29:29.522+00:00",[],"Development-of-a-system-for-measuring-calcitonin-in-the-stingray-Dasyatis-akajei-a-cartilaginous-fish-the-possible-involvement-of-stingray-calcitonin-in-gonadal-development",{"references":297,"abstract":299,"title":301,"doi":303,"gsPaper":305},{"VOID":298},"Azria M (1989) The calcitonins: physiology and pharmacology. Karger, Basel\nBentley PJ (1998) Hormones and osmoregulation. In: Bentley PJ (ed) Comparative vertebrates endocrinology, 3rd edn. Cambridge University Press, Cambridge, pp 337–378\nBjörnsson BTh, Haux C, Förlin L, Deftos LJ (1986) The involvement of calcitonin in the reproductive physiology of the rainbow trout. J Endocrinol 108:17–23\nChao CC, Brown RD, Deftos LJ (1985) Metabolism of calcium and phosphorus during pregnancy and lactation in white-tailed deer. Acta Endocrinol (Copenh) 109:269–275\nCopp DH, Cockcroft DW, Kueh Y (1967) Calcitonin from ultimobranchial glands of dogfish and chickens. Science 158:924–925\nDacke CG (1979) Calcium regulation in the chondrichthyes. In: Dacke CG (ed) Calciumn regulation in sub-mammalian vertebrates. Academic Press, London, pp 96–98\nDacke CG, Furr BJA, Boelkins JN, Kenny AD (1976) Sexually related changes in plasma calcitonin levels in Japanese quail. Comp Biochem Physiol Part A 55:341–344\nFiske CH, Subbarow Y (1925) The colorimetric determination of phosphorus. J Biol Chem 66:375–400\nGlowacki J, O’Sullivan J, Miller M, Wilkie DW, Deftos LJ (1985) Calcitonin produces hypercalcemia in leopard sharks. Endocrinology 116:827–829\nGreer FR, Lane J, Ho M (1984) Elevated serum parathyroid hormone, calcitonin, and 1,25-dihydroxyvitamin D in lactating women nursing twins. Am J Clin Nutr 40:562–568\nHazon N, Wells A, Pillans RD, Good JP, Anderson WG, Franklin CE (2003) Urea based osmoregulation and endocrine control in elasmobranch fish with special reference to euryhalinity. Comp Biochem Physiol Part B 136:685–700\nHiramatsu N, Todo T, Sullivan CV, Schilling J, Reading BJ, Matsubara T, Ryu YW, Mizuta H, Luo W, Nishimiya O, Wu M, Mushirobira Y, Yilmaz O, Hara A (2015) Ovarian yolk formation in fishes: molecular mechanisms underlying formation of lipid droplets and vitellogenin-derived yolk proteins. Gen Comp Endocrinol 221:9–15\nKase Y, Ikari T, Sekiguchi T, Sato M, Ogiso S, Kawada T, Matsubara S, Satake H, Sasayama Y, Endo M, Kitamura K, Hattori A, Watanabe TX, Maruyama Y, Watanabe Y, Funahashi H, Kambegawa A, Suzuki N (2017) Sardine procalcitonin amino-terminal cleavage peptide has a different action from calcitonin and promotes osteoblastic activity in the scales of goldfish. Comp Biochem Physiol Part A 211:77–83\nKwon HC, Hayashi S, Mugiya Y (1993) Vitellogenin induction by estradiol-17β in primary hepatocyte culture in the rainbow trout, Oncorhynchus mykiss. Comp Biochem Physiol Part B 104:381–386\nLu CC, Tsai SC, Wang SW, Tsai CL, Lau CP, Shih HC, Chen YH, Chiao YC, Liaw C, Wang PS (1998) Effects of ovarian steroid hormones and thyroxine on calcitonin secretion in pregnant rats. Am J Physiol 274:E246–E252\nNichols S, Gelsleichter J, Manire CA, Cailliet GM (2003) Calcitonin-like immunoreactivity in serum and tissues of the bonnethead shark, Sphyrna tiburo. J Exp Zool Part A 298:150–161\nNorberg B, Björnsson BTh, Brown CL, Wichardt U-P, Deftos LJ, Haux C (1989) Changes in plasma vitellogenin, sex steroids, calcitonin, and thyroid hormones related to sexual maturation in female brown trout (Salmo trutta). Gen Comp Endocrinol 75:316–326\nPersson P, Takagi Y, Björnsson BTh (1995) Tartrate resistant acid phosphatase as a marker for scale resorption in rainbow trout, Oncorhynchus mykiss: effects of estradiol-17β treatment and refeeding. Fish Physiol Biochem 14:329–339\nRobertson DR (1981) A competive inhibition enzyme-linked immunosorbent assay for frog calcitonin. Gen Comp Endocrinol 45:12–20\nSasayama Y (1999) Hormonal control of Ca homeostasis in lower vertebrates: considering the evolution. Zool Sci 16:857–869\nSasayama Y, Oguro C, Yui R, Kambegawa A (1984) Immunohistochemical demonstration of calcitonin in ultimobranchial glands of some lower vertebrates. Zool Sci 1:755–758\nSasayama Y, Suzuki N, Oguro C, Takei Y, Takahashi A, Watanabe TX, Nakajima K, Sakakibara S (1992) Calcitonin of the stingray: comparison of the hypocalcemic activity with other calcitonins. Gen Comp Endocrinol 86:269–274\nSearcy RL, Foreman JA, Ketz A, Reardon J (1967) A new automated method for urea nitrogen analysis. Tech Bull Regist Med Technol 37:107–111\nSekiguchi T, Suzuki N, Fujiwara N, Aoyama M, Kawada T, Sugase K, Murata Y, Sasayama Y, Ogasawara M, Satake H (2009) Calcitonin in a protochordate, Ciona intestinalis: the prototype of the vertebrate Calcitonin\u002FCalcitonin gene-related peptide superfamily. FEBS J 276:4437–4447\nSekiguchi T, Shiraishi A, Satake H, Kuwasako K, Takahashi H, Sato M, Urata M, Wada S, Endo M, Ikari T, Hattori A, Srivastav AK, Suzuki N (2017) Calcitonin-typical suppression of osteoclastic activity by amphioxus calcitonin superfamily peptides and insights into the evolutionary conservation and diversity of their structures. Gen Comp Endocrinol 246:294–300\nSuzuki N (2001) Calcitonin-like substance in the plasma of Cyclostomata and its putative role. Comp Biochem Physiol Part B 129:319–326\nSuzuki N, Takagi T, Sasayama Y, Kambegawa A (1995) Effects of ultimobranchialectomy on the mineral balances of the plasma and bile in the stingray (Elasmobranchii). Zool Sci 12:239–242\nSuzuki N, Ueda K, Sakamoto H, Sasayama Y (1999a) Fish calcitonin genes: primitive bony fish genes have been conserved in some lower vertebrates. Gen Comp Endocrinol 113:369–373\nSuzuki N, Suzuki D, Sasayama Y, Srivastav AK, Kambegawa A, Asahina K (1999b) Plasma calcium and calcitonin levels in eels fed a high calcium solution or transferred to seawater. Gen Comp Endocrinol 114:324–329\nSuzuki N, Suzuki T, Kurokawa T (2000) Suppression of osteoclastic activities by calcitonin in the scales of goldfish (freshwater teleost) and nibbler fish (seawater teleost). Peptides 21:115–124\nSuzuki N, Yamamoto K, Sasayama Y, Suzuki T, Kurokawa T, Kambegawa A, Srivastav AK, Hayashi S, Kikuyama S (2004) Possible direct induction by estrogen of calcitonin secretion from ultimobranchial cells in the goldfish. Gen Comp Endocrinol 138:121–127\nTakei Y, Takahashi A, Watanabe TX, Nakajima K, Sakakibara S, Sasayama Y, Suzuki N, Oguro C (1991) New calcitonin isolated from the ray, Dasyatis akajei. Biol Bull 180:485–488\nTinsley D (1985) A comparison of plasma levels of phosphoprotein, total protein and total calcium as indirect indices of exogenous vitellogenesis in the Crucian carp, Carassius carassius (L.). Comp Biochem Physiol Part B 80:913–916\nWang J, Rout UK, Bagchi IC, Armant DR (1998) Expression of calcitonin receptors in mouse preimplantation embryos and their function in the regulation of blastocyst differentiation by calcitonin. Development 125:4293–4302\nWatts EG, Copp DH, Deftos LJ (1975) Changes in plasma calcitonin and calcium during the migration of salmon. Endocrinology 96:214–218\nWendelaar Bonga SE, Pang PKT (1991) Control of calcium regulating hormones in the vertebrates: parathyroid hormone, calcitonin, prolactin, and stanniocalcin. Int Rev Cytol 128:139–213\nYamamoto K, Suzuki N, Takahashi N, Sasayama Y, Kikuyama S (1996) Estrogen receptors in the stingray (Dasyatis akajei) ultimobranchial gland. Gen Comp Endocrinol 101:107–114\nYamauchi H, Orimo H, Yamauchi K, Takano K, Takahashi H (1978) Increased calcitonin levels during ovarian development in the eel, Anguilla japonica. Gen Comp Endocrinol 36:526–529",{"EN":300},"To elucidate the physiological role of calcitonin (CT) in stingrays (cartilaginous fish), an enzyme-linked immunosorbent assay (ELISA) system using a specific antibody against stingray CT has been developed. Synthetic stingray CT was subcutaneously injected into mice four times—once every 2 weeks—together with an adjuvant. We purified the IgG antibody fraction using the protein A affinity chromatography from collected antiserum. Evaluating the antibody titer, we found the antibody’s optimum dilution ratio to be 600 times. Competitive ELISA has been developed using the antibody diluted 600 times. Our antibody did not cross-react with teleost CTs and muscle extraction, but cross-reacted with stingray plasma and the extract of the ultimobranchial gland, the secretary organ of stingray CT. Using this ELISA, we measured the plasma CT level in stingrays and examined its correlation with several mineral concentrations. Plasma CT did not show significant correlation to calcium, magnesium, inorganic phosphorus, sodium, chlorine, or urea, although there was a correlation among the factors involved in osmoregulation, such as sodium, chlorine, and urea. On the other hand, plasma CT was significantly correlated to body weight and length. Furthermore, there was a significant correlation between plasma CT and gonad weight. Since plasma CT was correlated with the weight of liver, which is involved in the synthesis of egg yolk protein, we examined the influence of 17β-estradiol (E2) on CT secretion. After E2 injection, the plasma CT level increased significantly. This is the first study to demonstrate that E2 induced plasma CT secretion in cartilaginous fish.",{"EN":302},"Development of a system for measuring calcitonin in the stingray Dasyatis akajei (a cartilaginous fish): the possible involvement of stingray calcitonin in gonadal development",{"VOID":304},"10.1007\u002Fs40071-019-00236-0",{"VOID":306},"6507348628921205107","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002Fs40071-019-00236-0",[309,328,347,360,379,397,410,425,443,462,481,500],{"id":310,"sortIndex":311,"researcher":22,"roles":312,"affiliations":313,"properties":325},"cebcede3-a319-405f-88c9-31c8b7b0619f",4,[132],[314],{"id":315,"sortIndex":23,"affiliation":316,"properties":22},"abfcfb88-f534-4505-a1eb-4517ebf07378",{"id":317,"createTime":318,"updateTime":319,"relativeEntities":320,"slug":321,"properties":322,"entityType":43,"verifyStatus":21,"verifyTime":22,"verifyNote":22,"syncStatus":21,"languages":22,"translateLanguages":22,"viewCount":23},"0a961865-c4fb-4883-bc02-16ff15f4a33f","2024-01-12T08:07:57.143+00:00","2025-06-11T23:29:22.114+00:00",[],"Peptide-Institute-Inc-Ibaraki-Japan",{"title":323},{"VI":324},"Peptide Institute Inc, Ibaraki, Japan",{"title":326},{"VI":327},"Takushi X. 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MY, Abol-Munafi AB, Ambak MA, Norazmi-Lokman NH (2011) The effects of stocking method on the gonad development of androgen treated false clownfish, Amphiprion ocellaris. Ind J Sci Tech 9th ISRPF Issue 4:145–146\nAjith Kumar TT, Balasubramanian T (2009) Broodstock development, spawning and larval rearing of the false clownfish, Amphiprion ocellaris in captivity using estuarine water. Curr Sci 97:1483–1486\nAngilletta MJ, Bennett AF, Guderly H, Navas CA, Seebacher F, Wilson RS (2006) Co adaptation: a unifying principle in evolutionary thermal biology. Physiol Biochem Zool 79:282–294\nBeamish FWH, Trippel EA (1990) Heat Increment: a static dynamic dimension in bioenergetic models? Trans Am Fish Soc 119:649–661\nBecker CD, Genoway RG (1979) Evaluation of the critical thermal maximum for determining thermal tolerance of freshwater fish. Environ Biol Fish 4:245–256\nBeitinger TL, Bennett WA (2000) Quantification of the role of acclimation temperature in temperature tolerance of fishes. Environ Biol Fish 58:277–288\nBeitinger TL, Fitzpatrick LC (1979) Physiological and ecological correlates of preferred temperature in fish. Am Zool 19:319–330\nBellgraph BJ, McMichael GA, Mueller RP, Monroe JL (2010) Behavioural response of juvenile Chinook salmon Oncorhynchus tshawytscha during sudden temperature increase and implications for survival. J Therm Biol 35:6–10\nBennett WA, Beitinger TL (1997) Temperature tolerance of the sheepshead minnow Cyprinodon variegatus. Copeia 1:77–87\nChabot D, Mckenzie DJ, Craig JF (2016a) Metabolic rate in fishes: definitions, methods and significance for conservation physiology. J Fish Biol 88:1–9\nChabot D, Steffensen JF, Farrell AP (2016b) The determination of standard metabolic rate in fishes. J Fish Biol 88:81–121\nChatterjee N, Pal AK, Manush SM, Das T, Mukherjee SC (2004) Thermal tolerance and oxygen consumption of Labeo rohita and Cyprinus carpio early fingerlings acclimated to three different temperatures. J Therm Biol 29:265–270\nColes SL, Riegl BM (2013) Thermal tolerances of reef corals in the Gulf: a review of the potential for increasing coral survival and adaptation to climate change through assisted translocation. Mar Poll Bull 72:323–332\nCrawshaw LI (1977) Physiological and behavioral reactions of fish to temperature change. J Fish Res Board Can 34:730–734\nDalvi RS, Pal AK, Tiwari LR, Das T, Baruah K (2009) Thermal tolerance and oxygen consumption rates of the catfish Horabagrus brachysoma (Gunther) acclimated to different temperatures. Aquaculture 295:116–119\nDas T, Pal AK, Chakraborty SK, Manush SM, Chatterjee N, Mukherjee SC (2004) Thermal tolerance and oxygen consumption of Indian Major Carps acclimated to four temperatures. J Therm Biol 29:157–163\nDas T, Pal AK, Chakraborty SK, Manush SM, Sahu NP, Mukherjee SC (2005) Thermal tolerance, growth and oxygen consumption of Labeo rohita acclimated to four temperatures. J Therm Biol 30:378–383\nDebnath D, Pal AK, Sahu NP, Baruah K, Yengkopam S, Das T, Manush SM (2006) Thermal tolerance and metabolic activity of yellowtail catfish Pangasius pangasius (Hamilton) advanced fingerlings with emphasis on their culture potential. Aquaculture 258:606–610\nDi Santo V, Lobel PS (2017) Body size and thermal tolerance in tropical gobies. J Exp Mar Biol Ecol 487:11–17\nDíaz F, Re A, González R, Sánchez L, Leyva G, Valenzuela F (2007) Temperature preference and oxygen consumption of the largemouth bass Micropterus salmoides (Lacépede) acclimated to different temperatures. Aqua Res 38:1387–1394\nEme J, Bennett WA (2009) Critical thermal tolerance polygons of tropical marine fishes from Sulawesi, Indonesia. J Therm Biol 34:220–225\nFarrell AP (2016) Pragmatic perspective on aerobic scope: peaking, plummeting, pejus and apportioning. J Fish Biol 88:322–333\nGoyer K, Bertolo A, Pepino M, Magnan P (2014) Effects of lake warming on behavioural thermoregulatory tactics in a cold-water stenothermic fish. PLoS ONE 9:e92514\nHabary A, Johansen JI, Nay TJ, Steffensen JF, Rummer JL (2017) Adapt, move or die-how will tropical coral reefs fishes cope with ocean warming? Glob Change Biol 23:566–577\nHalsey LG, Metthew PGD, Rezende EL, Chauvaud L, Ronson AA (2015) The interactions between temperature and activity levels in driving metabolic rate: theory with empirical validation from contrasting ectotherms. Oecologia 117:117–1129\nHalsey LG, Killen SS, Clark TD, Norin T (2018) Exploring key issues of aerobic scope interpretation in ectotherms: absolute versus factorial. Rev Fish Biol Fish 28:405–415\nHarborne AR (2013) The ecology, behavior and physiology of fishes on coral reef flats, and the potential impacts of climate change. J Fish Biol 83:417–447\nHobbs JPA, Frisch AJ, Ford BM, Thums M, Saenz-Agudelo P, Furby KA, Berumen ML (2015) Taxonomic, Spatial and Temporal Patterns of Bleaching in Anemones Inhabited by Anemonefishes. PLoS ONE 8:e70966\nHuey RB, Kearny MR, Krockenberger A, Holtum JAM, Williams SE (2012) Predictions of organismal vulnerability to climate warming: roles of behavior, physiology and adaptation. Phil Trans Royal Soc B. 367:1665–1679\nJung HL (2006) Spawning, development and larval rearing of false clownfish Amphiprion ocellaris under captive conditions. Dissertation. Universiti Malaysia Terengganu, Malaysia\nKearney M, Shine R, Porter WP (2009) The potential for behavioral thermoregulation to buffer ‘cold-blooded’ animals against climate warming. PNAS 106:3835–3840\nKhan JR, Herbert NA (2012) The behavioural thermal preference of the common triplefin (Forsterygion lapillum) tracks aerobic scope optima at the upper thermal limits of its distribution. J Therm Biol 37:118–124\nKir M, Sunar MC, Altindağ BC (2017) Thermal tolerance and preferred temperatures range of juvenile meagre acclimated to four temperatures. J Therm Biol 65:125–129\nLarios-Soriano E (2014) Temperatura preferida, temperaturas criticas y respuestas metabolicas de Lutjanus guttatus (Steindachner, 1869) ante diferentes temperaturas de aclimatacion. Dissertation. Centro de Investigacion Cientifica y de Educacion Superior de Ensenada\nLasker HR, Peters EC, Coffroth MA (1984) Bleaching of reef coelenterates in the San Blas Islands, Panama. Coral Reefs 3:183–190\nLi AJ, Leung PTY, Bao VWW, Lui GCS, Leung KMY (2015) Temperature dependent physiological and biochemical responses of the marine medaka Oryzias melatostigma with consideration of both low and high thermal extremes. J Therm Biol 54:98–105\nLuttterschmidt WI, Hutchison VM (1997) The critical thermal maximum: data to support the onset of spasms the definitive end point. Can J Zool 75:1553–1560\nMadeira C, Madeira D, Diniz MS, Cabral HN, Vinagre C (2016) Thermal acclimation in clownfish: an integrated biomarker response and multi-tissue experimental approach. Ecol Ind 71:280–292\nMadeira C, Madeira D, Diniz MS, Cabral HN, Vinagre C (2017) Comparing biomarker responses during thermal acclimation: a lethal vs non-lethal approach in tropical reef clownfish. Comp Biochem Physiol A 204:104–112\nMcKenzie DJ, Cataldi E, Romano P, Owen SF, Taylor EW, Bronzi P (2001) Effects of acclimation to brackish water on the growth, respiratory metabolism, and swimming performance of young-of-the-year Adriatic sturgeon Acipenser naccari. Can J Fish Aqua Sci 58:1104–1112\nMedvick P, Miller JM (1979) Behavioral thermoregulation in three Hawaiian reef fishes. Environ Biol Fish 4:23–28\nMora C, Ospina AF (2001) Tolerance to high temperatures and potentially impact to sea warming on reef fishes of Gorgona Island (tropical eastern Pacific). Mar Biol 139:765–769\nNay TJ, Johansen JI, Habary A, Steffensen JR, Rummer JI (2015) Behavioural thermoregulation in a temperature-sensitive coral reef fish the five lined cardinalfish Chailodipterus quinquelineatus. Coral Reefs 34:1261–1265\nNelson SG, Simmons MA, Knight AW (1985) Calorigenic effect of diet on the grass shrimp Crangon franciscorum (Crustacea: Crangonidae). Comp Biochem Physiol 82:373–376\nNilsson GE, Crawley N, Lunde IG, Munday PL (2009) Elevated temperatures reduce the respiratory scope of coral reef fishes. Glob Change Biol 15:1405–1412\nNorin T, Clark TD (2016) Measurement and relevance of maximum metabolic rate in fish. J Fish Biol 88:122–151\nNorin T, Malte H, Clark TD (2014) Aerobic scope does not predict the performance of a tropical eurythermal fish at elevate temperatures. J Exp Biol 217:244–251\nNoyola Regil J, Mascaro M, Díaz F, Re AD, Sanchez-Zamora A, Caamal-Monsreal C, Rosas C (2015) Thermal biology of prey (Melongena corona bispinosa, Strombus pugilis, Callinectes similis, Libinia dubia) and predators (Ocyurus chrysurus, Centropomus undecimalis) of Octopus maya from the Yucatan Peninsula. J Therm Biol 53:151–161\nPaladino FV, Spotila JR, Schubauer JP, Kowalski KT (1980) The critical thermal maximum: a technique used to elucidate physiological stress and adaptation in fishes. Rev Can Biol 39:115–122\nPaschke K, Argüero J, Guebauer P, Díaz F, Mascaro M, López-Ripoll E, Sánchez-Tapia I, Caamal-Monsreal C, Tremblay N, Hans-Otto Pörtner, Rosas C (2018) Estimating the aerobic scope for metabolic activity in aquatic ectotherms: a novel approach. Front Physiol 9:1438\nPérez E, Díaz F, Espina S (2003) Thermoregulatory behavior and critical thermal limits of angelfish Pterophyllum scalare (Lichtenstein) (Pisces: Cichlidae). J Therm Biol 28:531–537\nPíaseĉnà K, Ponĉvà A, Tejdo M, Gvoždik l (2015) Thermoregulatory strategies in an aquatic hábitats: an evaluation of current approaches. J Therm Biol 52:97–107\nPörtner HO (2010) Oxygen- and capacity-limitation of thermal tolerance: a matrix for integrating climate-related stressor effects in marine ecosystems. J Exp Biol 213:881–893\nPörtner HO, Knust R (2007) Climate change affects marine fishes through oxygen limitation of thermal tolerance. Science 315:95–97\nReynolds WW (1979) Perspective and introduction to the symposium: thermoregulation in ectotherms. Am Zool 19:193–194\nReynolds WW, Casterlin ME (1979) Behavioral thermoregulation and the final preferendum paradigm. Am Zool 19:211–224\nRummer JL, Couturier CS, Stecyk JAW, Gardiner NR, Kinch JP, Nilsson GE, Munday PL (2014) Thermal optima for aerobic scope of equatorial reef fishes are close to current day temperatures. Glob Change Biol 20:1055–1066\nRushworth KJW, Smith DA, Cowden KL, Purcell SW (2011) Optimal temperature for growth and condition of an endemic subtropical anemonefish. Aquaculture 318:479–482\nSarma K, Pal AK, Ayyappan S, Das T, Manush SM, Debnath D, Baruah K (2010) Acclimation of Anabas testudineus (Bloch) to three test temperatures influences thermal tolerance and oxygen consumption. Fish Physiol Biochem 36:85–90\nSchurmann H, Steffensen JF (1997) Effects of temperature, hypoxia and activity on the metabolism of juvenile Atlantic cod. J Fish Biol 50:1166–1180\nSokolova IM, Frederich M, Bagwe R, Lannig G, Sukhotin AA (2012) Energy homeostasis as an integrative tool for assessing limits of environmental stress tolerance in aquatic invertebrates. Mar Environ Res 79:1–15\nSunday JM, Bates A, Kearny MR, Colwell RK, Dulvy NK, Longino JT, Huey RB (2014) Thermal-safety margins and they necessity of thermoregulatory behaviour across latitude and elevation. PNAS 111:5610–5615\nVinagre C, Leal I, Mendonça V, Madeira D, Narciso L, Diniz MS, Flores AAV (2016) Vulnerability to climate warming and acclimation capacity of tropical and temperate coastal organisms. Ecol Ind 62:317–327\nWard AJW, Hensor EMA, Webster MN, Hart PJB (2010) Behavioural thermoregulation in two freshwater fish species. J Fish Biol 76:2287–2298\nXu W, Dang W, Geng J, Lu HG (2015) Thermal preference, thermal resistance and metabolic rate of juvenile Chinese pond turtles Mauremys reevesiiacclimated to different temperatures. J Therm Biol 53:119–124",{"EN":567},"The clownfish Amphiprion ocellaris is widely distributed in the coral reef ecosystems of tropical and subtropical regions of the West Indo Pacific, an area that hosts economically valuable species, and, thus, a suitable candidate for warm water aquaculture. This study determined the preferred temperature, critical threshold limits, represented by critical thermal maximum and critical thermal minimum, thermal window width, and aerobic metabolic scope of A. ocellaris clownfish acclimated to 20, 23, 26, 29, 32, and 35 °C. A positive response (P \u003C 0.05) occurred when the preferred temperature significantly increased with increasing acclimation temperature. The preferred temperature obtained graphically was 30.0 °C. Acclimation temperature significantly affected the thermal tolerance which increased with acclimation temperature. The thermal window calculated for A. ocellaris was 301.5 °C2. The thermal metabolic scope obtained in animals acclimated at the interval from 23 to 32 °C (P > 0.05) had a mean value of 4240.8 mg O2 h−1 kg−1 w.w., revealing that A. ocellaris is a eurythermal species with a range of optimal physiological performance that closely matches the environmental conditions where it can be farmed. Therefore, the highest value of the thermal aerobic scopes corresponded to the intervals of the preferred temperature obtained for A. ocellaris. These results may partially explain their worldwide distribution pattern, as well as their aquaculture potential in tropical regions.",{"EN":569},"Thermal preference, tolerance, and thermal aerobic scope in clownfish Amphiprion ocellaris (Cuvier, 1830) predict its aquaculture potential across tropical regions",{"VOID":571},"10.1007\u002Fs40071-019-0228-7","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002Fs40071-019-0228-7",[574,589,601,613,625,640,655],{"id":575,"sortIndex":311,"researcher":22,"roles":576,"affiliations":577,"properties":586},"a48930b9-0fbb-495a-9357-d4aa508cf06b",[132],[578],{"id":22,"sortIndex":23,"affiliation":579,"properties":22},{"id":580,"createTime":581,"updateTime":581,"relativeEntities":582,"slug":22,"properties":583,"entityType":43,"verifyStatus":21,"verifyTime":22,"verifyNote":22,"syncStatus":21,"languages":22,"translateLanguages":22,"viewCount":23},"4f67a650-9b38-45a5-8f60-147d9df64217","2024-01-14T23:24:45.856+00:00",[],{"title":584},{"VI":585},"Laboratorio de Reproducción y Producción de Larvas de Peces Marinos, Centro de Investigación en Alimentación y Desarrollo A. 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Velasco-Blanco",{"id":626,"sortIndex":169,"researcher":22,"roles":627,"affiliations":628,"properties":637},"df150ecd-72bd-4a71-b807-368a4e7f7f76",[132],[629],{"id":22,"sortIndex":23,"affiliation":630,"properties":22},{"id":631,"createTime":632,"updateTime":632,"relativeEntities":633,"slug":22,"properties":634,"entityType":43,"verifyStatus":21,"verifyTime":22,"verifyNote":22,"syncStatus":21,"languages":22,"translateLanguages":22,"viewCount":23},"7383a1f7-4e1b-42b7-816e-32dea5a584d7","2024-01-14T23:24:45.842+00:00",[],{"title":635},{"VI":636},"Laboratorio de Ecofisiología de Organismos Acuáticos, Departamento de Biotecnología Marina, Centro de Investigación Científica y de Educación Superior de Ensenada (CICESE), Ensenada, Mexico",{"title":638},{"VI":639},"Fernando Díaz",{"id":641,"sortIndex":99,"researcher":22,"roles":642,"affiliations":643,"properties":652},"d4a2a237-e6de-4ec2-b964-b63126d5c935",[132],[644],{"id":22,"sortIndex":23,"affiliation":645,"properties":22},{"id":646,"createTime":647,"updateTime":647,"relativeEntities":648,"slug":22,"properties":649,"entityType":43,"verifyStatus":21,"verifyTime":22,"verifyNote":22,"syncStatus":21,"languages":22,"translateLanguages":22,"viewCount":23},"7c5bb5da-139e-484b-b2cb-c860af7d4cc5","2024-01-14T23:24:45.898+00:00",[],{"title":650},{"VI":651},"Unidad Multidisciplinaria de Docencia e Investigación, Facultad de Ciencias, Universidad Nacional Autónoma de México, Sisal, Mexico",{"title":653},{"VI":654},"Carlos Rosas",{"id":656,"sortIndex":44,"researcher":22,"roles":657,"affiliations":658,"properties":664},"17ddff77-ef66-4dfb-a223-bbd2977be7fc",[132],[659],{"id":22,"sortIndex":23,"affiliation":660,"properties":22},{"id":631,"createTime":632,"updateTime":632,"relativeEntities":661,"slug":22,"properties":662,"entityType":43,"verifyStatus":21,"verifyTime":22,"verifyNote":22,"syncStatus":21,"languages":22,"translateLanguages":22,"viewCount":23},[],{"title":663},{"VI":636},{"title":665},{"VI":666},"Ana Denise Re",{"url":572,"publisher":668,"properties":697},{"id":6,"createTime":7,"updateTime":8,"relativeEntities":669,"slug":10,"properties":670,"entityType":20,"verifyStatus":21,"verifyTime":22,"verifyNote":22,"syncStatus":21,"languages":22,"translateLanguages":22,"viewCount":23,"subjectFields":675,"manageAffiliations":676,"indexDatabases":677,"url":22,"thumbnailPath":22,"statistic":692,"gsStatistic":22,"type":108,"analyzePriority":22},[],{"issn":671,"eissn":672,"title":673,"url":674},{"VOID":13},{"VOID":15},{"EN":17},{"VOID":19},[],[],[678,685],{"id":58,"indexDatabase":679,"url":22,"indexYears":22,"academicFieldIds":684,"indexDatabaseRanking":22},{"id":60,"createTime":61,"updateTime":62,"relativeEntities":680,"label":681,"description":682,"key":69,"publicationTags":683,"standard":22},[],{"EN":65,"VI":65},{"VI":67,"EN":68},[71,72],[74],{"id":76,"indexDatabase":686,"url":89,"indexYears":90,"academicFieldIds":691,"indexDatabaseRanking":93},{"id":78,"createTime":79,"updateTime":80,"relativeEntities":687,"label":688,"description":689,"key":86,"publicationTags":690,"standard":22},[],{"EN":83,"VI":83},{"EN":83,"VI":85},[88],[92],{"impactFactor":23,"impactFactorByYear":693,"i10Index":23,"i10IndexLast5Year":23,"totalPublication":96,"totalPublicationByYear":694,"totalCitation":23,"totalCitationByYear":695,"totalCitationPerPublication":23,"totalCitationPerPublicationByYear":696,"hindexLast5Year":23,"hindex":23},{},{"2012":98,"2013":99,"2014":100,"2015":101,"2016":102,"2017":103,"2018":104,"2019":105},{},{},{"volume":698,"pages":699},{"VOID":551},{"VOID":700},"187-197","2019-06-14",{"id":703,"createTime":704,"updateTime":705,"relativeEntities":706,"slug":707,"properties":708,"entityType":126,"verifyStatus":234,"verifyTime":705,"verifyNote":235,"syncStatus":21,"languages":22,"translateLanguages":22,"viewCount":23,"primaryUrl":717,"fullTextUrl":22,"authors":718,"publicationType":180,"publisherRelationship":759,"citationCount":22,"citationInfo":22,"publishDate":794,"publishYear":795,"citationAnalyzeStatus":21,"lastCitationAnalyze":22,"indexDatabases":22,"openAccess":22,"references":22,"isForceReanalyzing":218},"ddb710df-0a3d-4e10-8aae-3debbfd9fb27","2023-11-27T03:14:34.635+00:00","2024-12-17T23:23:44.744+00:00",[],"Characterization-of-Vibrio-parahaemolyticus-isolated-from-farmed-sea-bass-Dicentrarchus-labrax-during-disease-outbreaks",{"references":709,"abstract":711,"title":713,"doi":715},{"VOID":710},"Alcaide E, Amaro C, Todoli R, Oltra R: Isolation and characterization of Vibrio parahaemolyticus causing infection in Iberian toothcarp Aphanius iberus . Dis Aquat Organ 1999,35(1):77–80. doi:10.3354\u002Fdao035077 doi:10.3354\u002Fdao035077\nAlsina M, Blanch AR: A set of keys for biochemical identification of environmental Vibrio species. J Appl Bacteriol 1994,76(1):79–85. 10.1111\u002Fj.1365-2672.1994.tb04419.x\nAmaro C, Biosca EG, Fouz B, Alcaide E, Esteve C: Evidence that water transmits Vibrio vulnificus biotype 2 infections to eels. Appl Environ Microbiol 1995,61(3):1133–1137.\nAustin B, Austin DA: Bacterial fish pathogens, disease of farmed and wild fish. 4th edition. Godalming: Springer Praxis; 2007.\nBaffone W, Pianetti A, Bruscolini F, Barbieri E, Citterio B: Occurrence and expression of virulence-related properties of Vibrio species isolated from widely consumed seafood products. Int J Food Microbiol 2000,54(1–2):9–18. doi:10.1016\u002FS0168–1605(99)00189–0 doi:10.1016\u002FS0168-1605(99)00189-0 10.1016\u002FS0168-1605(99)00189-0\nBen Kahla-Nakbi A, Besbes A, Bakhrouf A, Alcaide E: Characterization and virulence properties of Vibrio strains isolated from diseased gilthead sea bream ( Sparus aurata ) cultured in Tunisia. Bull Eur Assoc Fish Pathol 2007, 27: 90–99.\nBen Kahla-Nakbi A, Chaieb K, Bakhrouf A: Investigation of several virulence properties among Vibrio alginolyticus strains isolated from diseased cultured fish in Tunisia. Dis Aquat Organ 2009,86(1):21–28.\nBordas MA, Balebona MC, Zorrilla I, Borrego JJ, Morinigo MA: Kinetics of adhesion of selected fish-pathogenic Vibrio strains of skin mucus of gilt-head sea bream ( Sparus aurata L .). Appl Environ Microbiol 1996,62(10):3650–3654.\nCai J, Li J, Thompson KD, Li C, Han H: Isolation and characterization of pathogenic Vibrio parahaemolyticus from diseased post-larvae of abalone Haliotis diversicolor supertexta . J Basic Microbiol 2007,47(1):84–86. doi:10.1002\u002Fjobm.200610192 doi:10.1002\u002Fjobm.200610192 10.1002\u002Fjobm.200610192\nChristensen WB: Urea decomposition as a means of differentiating Proteus and paracolon cultures from each other and from Salmonella and Shigella types. J Bacteriol 1946,52(4):461–466.\nCroci L, Suffredini E, Cozzi L, Toti L, Ottaviani D, Pruzzo C, Serratore P, Fischetti R, Goffredo E, Loffredo G, Mioni R: Comparison of different biochemical and molecular methods for the identification of Vibrio parahaemolyticus . J Appl Microbiol 2006,102(1):229–237. doi:10.1111\u002Fj.1365–2672.2006.03046.x doi:10.1111\u002Fj.1365-2672.2006.03046.x\nDePaola A, Nordstrom JL, Bowers JC, Wells JG, Cook DW: Seasonal abundance of total and pathogenic Vibrio parahaemolyticus in Alabama oysters. Appl Environ Microbiol 2003,69(3):1521–1526. 10.1128\u002FAEM.69.3.1521-1526.2003\nDileep V, Kumar HS, Kumar Y, Nishibuchi M, Karunasagar I: Application of polymerase chain reaction for detection of Vibrio parahaemolyticus associated with tropical seafoods and coastal environment. Lett Appl Microbiol 2003,36(6):423–427. doi:10.1046\u002Fj.1472–765X.2003.01333.x doi:10.1046\u002Fj.1472-765X.2003.01333.x 10.1046\u002Fj.1472-765X.2003.01333.x\nFood and Drug Administration: Bacteriological analytical manual. 2nd edition. Washington DC: Association of Official Analytical Chemists; 1992.\nHammack TS, Amaguana RM, Andrews WH: An improved method for the recovery of Salmonella serovars from orange juice using universal preenrichment broth. J Food Prot 2001,64(5):659–663.\nHara-Kudo Y, Sugiyama K, Nishina T, Saitoh A, Nakagawa H, Ichihara T, Konuma H, Hasegawa J, Kumagai S: Detection of TDH-producing Vibrio parahaemolyticus O3:K6 from naturally contaminated shellfish using an immunomagnetic separation method and chromogenic agar medium. Kansenshogaku Zasshi 2001,75(11):955–960.\nHervio-Heath D, Colwell RR, Derrien A, Robert-Pillot A, Fournier JM, Pommepuy M: Occurrence of pathogenic Vibrios in coastal areas of France. J Appl Microbiol 2002,92(6):1123–1135. doi:10.1046\u002Fj.1365–2672.2002.01663.x doi:10.1046\u002Fj.1365-2672.2002.01663.x 10.1046\u002Fj.1365-2672.2002.01663.x\nHormansdorfer S, Wentges H, Neugebaur-Buchler K, Bauer J: Isolation of Vibrio alginolyticus from seawater aquaria. Int J Hyg Environ Health 2000,203(2):169–175. 10.1078\u002FS1438-4639(04)70024-3\nJayasree S: Identification of immune cells interacting with Vibrio spp. and its in vitro post-phagocytic killing mechanism of haemocytes in the penaeid shrimp, Penaeus indicus H. Milne Edwards. J Fish Dis 2009,32(4):359–365. doi:10.1111\u002Fj.1365–2761.2009.01018.x. doi:10.1111\u002Fj.1365-2761.2009.01018.x. 10.1111\u002Fj.1365-2761.2009.01018.x\nKarunasagar I, Sugumar G, Reilly PJ: Rapid polymerase chain reaction method for detection of Kanagawa positive Vibrio parahaemolyticus in seafoods. Int J Food Microbiol 1996,31(1–3):317–323.\nKim YB, Okuda J, Matsumoto C, Takahashi N, Hashimoto S, Nishibuchi M: Identification of Vibrio parahaemolyticus strains at the species level by PCR targeted to the toxR gene. J Clin Microbiol 1999,37(4):1173–1177.\nLee CY, Cheng MF, Yu MS, Pan MJ: Purification and characterization of a putative virulence factor, serine protease, from Vibrio parahaemolyticus . FEMS Microbiol Lett 2002,209(1):31–37. doi:10.1016\u002FS0378–1097(02)00477–9 doi:10.1016\u002FS0378-1097(02)00477-9 10.1111\u002Fj.1574-6968.2002.tb11105.x\nMartinez-Urtaza J, Simental L, Velasco D, DePaola A, Ishibashi M, Nakaguchi Y, Nishibuchi M, Carrera-Flores D, Rey-Alvarez C, Pousa A: Pandemic Vibrio parahaemolyticus O3:K6, Europe. Emerg Infect Dis 2005,11(8):1319–1320. 10.3201\u002Feid1108.050322\nMatsumoto C, Okuda J, Ishibashi M, Iwanaga M, Garg P, Rammamurthy T, Wong HC, Depaola A, Kim YB, Albert MJ, Nishibuchi M: Pandemic spread of an O3:K6 clone of Vibrio parahaemolyticus and emergence of related strains evidenced by arbitrarily primed PCR and toxRS sequence analyses. J Clin Microbiol 2000,38(2):578–585.\nNair GB, Ramamurthy T, Bhattacharya SK, Dutta B, Takeda Y, Sack DA: Global dissemination of Vibrio parahaemolyticus serotype O3:K6 and its serovariants. Clin Microbiol Rev 2007,20(1):39–48. doi:10.1128\u002FCMR.00025–06 doi:10.1128\u002FCMR.00025-06\nNishibuchi M, Kaper JB: Thermostable direct hemolysin gene of Vibrio parahaemolyticus : a virulence gene acquired by a marine bacterium. Infect Immun 1995,63(6):2093–2099.\nOkuda J, Ishibashi M, Abbott SL, Janda JM, Nishibuchi M: Analysis of the thermostable direct hemolysin ( tdh ) gene and the tdh -related hemolysin ( trh ) genes in urease-positive strains of Vibrio parahaemolyticus isolated on the West Coast of the United States. J Clin Microbiol 1997,35(8):1965–1971.\nOttaviani D, Santarelli S, Bacchiocchi S, Masini L, Ghittino C, Bacchiocchi I: Presence of pathogenic Vibrio parahaemolyticus strains in mussels from the Adriatic Sea, Italy. Food Microbiol 2005, 22: 585–590. 10.1016\u002Fj.fm.2005.01.005\nQuilici ML, Robert-Pillot A, Picart J, Fournier JM: Pandemic Vibrio parahaemolyticus O3:K6 spread, France. Emerg Infect Dis 2005,11(7):1148–1149. 10.3201\u002Feid1107.041008\nQuindos G, Salesa R, Carrillo-Munoz AJ, Lipperheide V, Jaudenes L, San Millan R, Torres-Rodriguez JM, Ponton J: Multicenter evaluation of ATB fungus: a standardized micromethod for yeast susceptibility testing. Chemotherapy 1994,40(4):245–251. 10.1159\u002F000239200\nReed M, Muench H: A simple method for estimating fifty per cent endpoints. Am J Hyg 1938, 27: 493–497.\nRobert-Pillot A, Guenole A, Lesne J, Delesmont R, Fournier JM, Quilici ML: Occurrence of the tdh and trh genes in Vibrio parahaemolyticus isolates from waters and raw shellfish collected in two French coastal areas and from seafood imported into France. Int J Food Microbiol 2004,91(3):319–325. doi:10.1016\u002Fj.ijfoodmicro.2003.07.006 doi:10.1016\u002Fj.ijfoodmicro.2003.07.006 10.1016\u002Fj.ijfoodmicro.2003.07.006\nZhang XH, Austin B: Haemolysins in Vibrio species. J Appl Microbiol 2005,98(5):1011–1019. doi:10.1111\u002Fj.1365–2672.2005.02583.x doi:10.1111\u002Fj.1365-2672.2005.02583.x 10.1111\u002Fj.1365-2672.2005.02583.x\nZorrilla I, Arijo S, Chabrillon M, Diaz P, Martinez-Manzanares E, Balebona MC, Morinigo MA: Vibrio species isolated from diseased farmed sole, Solea senegalensis (Kaup), and evaluation of the potential virulence role of their extracellular products. J Fish Dis 2003,26(2):103–108. 10.1046\u002Fj.1365-2761.2003.00437.x",{"EN":712},"Vibrio parahaemolyticus was isolated from the internal organs of diseased sea bass (Dicentrarchus labrax) cultured in a marine cage farm and an inshore fish farm in the summer 2010. All strains isolated from diseased sea bass were tested for virulence by intraperitoneal injection. The isolates (n = 6) were pathogenic for sea bass. Only bacterial strains showing haemolytic activity were virulent. LD50 values ranged from 3.52 × 104 to 2.29 × 106 cfu fish−1. In this study, we report the characterization and the virulence of V. parahaemolyticus strains isolated from sea bass originating from two different fish farms (marine cage farm and inshore fish farm in Tunisia).",{"EN":714},"Characterization of Vibrio parahaemolyticus isolated from farmed sea bass (Dicentrarchus labrax) during disease outbreaks",{"VOID":716},"10.1186\u002F2008-6970-5-13","http:\u002F\u002Fwww.intaquares.com\u002Fcontent\u002F5\u002F1\u002F13",[719,735,747],{"id":720,"sortIndex":44,"researcher":22,"roles":721,"affiliations":722,"properties":732},"c7038f9e-85c6-480a-9308-58b7d98c58ac",[132],[723],{"id":22,"sortIndex":23,"affiliation":724,"properties":22},{"id":725,"createTime":726,"updateTime":726,"relativeEntities":727,"slug":728,"properties":729,"entityType":43,"verifyStatus":21,"verifyTime":22,"verifyNote":22,"syncStatus":21,"languages":22,"translateLanguages":22,"viewCount":23},"7a11da4f-addd-49dc-ab20-36456af07663","2023-11-27T03:14:34.647+00:00",[],"D%C3%A9partement-de-Microbiologie-Facult%C3%A9-de-Pharmacie-Laboratoire-d-Analyse-Traitement-et-Valorisation-des-Polluants-de-l-Environnement-et-des-Produits-Monastir-Tunisia",{"title":730},{"VI":731},"Département de Microbiologie, Faculté de Pharmacie, Laboratoire d'Analyse, Traitement et Valorisation des Polluants de l'Environnement et des 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GS, Williams GJ, Franklin EC, Haapkyla J, Harvell CD, Neale S, Page CA, Raymundo L, Vargas-Ángel B, Willis B, Work TM, Davy SK (2011) Growth anomalies on the coral genera Acropora and Porites are strongly associated with host density and human population size across the Indo-Pacific. PLoS One 6:e16887. doi:10.1371\u002Fjournal.pone.0016887\nGoreau TJ, Cervino J, Goreau M, Hayes R, Hayes M, Richardson L, Smith G, DeMeyer K, Nagelkerken I, Garzon-Ferrera J, Gil D, Garrison G, Williams EH, Bunkley-Williams L, Quirolo C, Patterson K, Porter JM, Porter K (1998) Rapid spread of diseases in Caribbean coral reefs. Rev Biol Trop 46:157–171\nGreen EP, Bruckner AW (2000) The significance of coral disease epizootiology for coral reef conservation. Biol Cons 96:347–361. doi:10.1016\u002FS0006-3207(00)00073-2\nIrikawa A, Casareto BE, Suzuki Y, Agostini S, Hidaka M, van Woesik R (2011) Growth anomalies on Acropora cytherea corals. Mar Poll Bull 62(8):1702–1707. doi:10.1016\u002Fj.marpolbul.2011.05.033\nKaczmarsky L, Richardson LL (2007) Transmission of growth anomalies between Indo-Pacific Porites corals. J Invertebr Pathol 94(3):218–221. doi:10.1016\u002Fj.jip.2006.11.007\nKavousi J, Rezai H (2011) Coral lesions around some Iranian Islands in the Persian Gulf. Galaxea 13:5–6\nKavousi J, Seyfabadi J, Rezai H, Fenner D (2011) Coral reefs and communities of Qeshm Island, the Persian Gulf. Zool Stud 50:276–283\nKavousi J, Tavakoli-Kolour P, Barkhordari A, Bahrami A (2013) Mass mortality of Porites Corals on northern Persian Gulf reefs due to sediment-microbial interactions. Int J Mar Sci 3:306–310. doi:10.5376\u002Fijms.2013.03.0038\nKavousi J, Tavakoli-Kolour P, Mohammadizadeh M, Bahrami A, Barkhordari A (2014) Mass coral bleaching in the northern Persian Gulf, 2012. Sci Mar 78(3):397–404. doi:10.3989\u002Fscimar.03914.16A\nLoya Y, Bull G, Pichon M (1984) Tumor formations in scleractinian corals. Helgol Mar Res 37:99–112. doi:10.1007\u002FBF01989297\nMcClanahan TIM, Weil E, Maina J (2009) Strong relationship between coral bleaching and growth anomalies in massive Porites. Gobal Change Biol 15:1804–1816\nRezai H, Wilson S, Claereboudt M, Riegl B (2004) Coral reef status in the ROPME sea area, Arabian\u002FPersian Gulf, Gulf of Oman and Arabian Sea. In: Wilkinson C (ed) Status of coral reefs of the world, vol 1. Australian Institute of Marine Science, Washington DC, USA, pp 155–170\nRiegl BM, Bruckner AW, Samimi-Namin K, Purkis SJ (2012) Diseases, harmful algae blooms (HABs) and their effects on Gulf coral populations and communities. In: Riegl BM, Purkis SJ (eds) Coral reefs of the Gulf. Springer, Netherlands, pp 107–125\nSamimi-Namin K, Risk MJ, Hoeksema BW, Zohari Z, Rezai H (2010) Coral mortality and serpulid infestations associated with red tide, in the Persian Gulf. Coral Reefs 29:509. doi:10.1007\u002Fs00338-010-0601-x\nStimson J (2011) Ecological characterization of coral growth anomalies on Porites compressa in Hawaii. Coral Reefs 30(1):133–142. doi:10.1007\u002Fs00338-010-0672-8\nSutherland KP, Porter JW, Torres C (2004) Disease and immunity in Caribbean and Indo-Pacific zooxanthellate corals. Mar Ecol Prog Ser 266:273–302. doi:10.3354\u002Fmeps266273\nWeil E, Smith GW, Gil-Agudelo DL (2006) Status and progress in coral reef disease research. Dis Aquat Org 69:1–7. doi:10.3354\u002Fdao069001\nWeil E, Irikawa A, Casareto B, Suzuki Y (2012) Extended geographic distribution of several Indo-Pacific coral reef diseases. Dis Aquat Org 98(2):163–170. doi:10.3354\u002Fdao02433\nWillis BL, Page CA, Dinsdale EA (2004) Coral disease on the Great Barrier Reef. In: Rosenberg E, Loya Y (eds) Coral health and disease. Springer, Berlin, pp 69–104",{"EN":806},"Reports on the outbreaks of coral diseases are on the rise, stating that diseases are considered to be one of the main drives in the decline of global coral reefs. 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Further investigation is needed to understand the cause of GAs, their progress trend, and prospective impacts on the coral communities at our studied site.",{"EN":808},"Outbreak of growth anomalies in coral communities of Qeshm Island, Persian 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Ecol Model 269:1–8",{"doi":1112},"10.1016\u002Fj.ecolmodel.2013.07.025",{"id":22,"text":1114,"url":22,"identifiers":1115},"Okay OS, Gaines A (1996) Toxicity of 2,4-D to phytoplankton. Water Res 30:686–696",{},{"id":22,"text":1117,"url":22,"identifiers":1118},"Okay OS, Morkoc E, Gaines A (1994) Effects of two herbicidal waste waters on Chlorella sp. and Phaeodactylum tricornutum. Env Poll 84:1–6",{"doi":1119},"10.1016\u002F0269-7491(94)90063-9",{"id":22,"text":1121,"url":22,"identifiers":1122},"Okay OS, Gaines A, Davie AM (2003) The growth of continuous cultures of the phytoplankton Phaeodactylum tricornutum. Turkish J Eng Env Sci 27:145–155",{},{"id":22,"text":1124,"url":22,"identifiers":1125},"Okay OS, Gibson M, Gaines A, Davie AM (2005) Introduction to competition between continuous cultures of Phaeodactylum tricornutum and Dunaliella tertiolecta. 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Dynam Stabil Syst 8:189–217",{"doi":1158},"10.1080\u002F02681119308806158",{"id":1160,"createTime":1161,"updateTime":1162,"relativeEntities":1163,"slug":1164,"properties":1165,"entityType":126,"verifyStatus":234,"verifyTime":1162,"verifyNote":235,"syncStatus":21,"languages":1177,"translateLanguages":22,"viewCount":23,"primaryUrl":1178,"fullTextUrl":22,"authors":1179,"publicationType":180,"publisherRelationship":1312,"citationCount":99,"citationInfo":1347,"publishDate":1349,"publishYear":1350,"citationAnalyzeStatus":21,"lastCitationAnalyze":22,"indexDatabases":22,"openAccess":22,"references":1351,"isForceReanalyzing":218},"57664002-24c3-4626-96ad-2f2892a38483","2024-04-19T20:57:27.882+00:00","2025-01-06T22:48:48.368+00:00",[],"Hemolymph-osmotic-ionic-status-and-branchial-Na-K-ATPase-activity-under-varying-environmental-conditions-in-the-intertidal-grapsid-crab-Gaetice-depressusd",{"mag":1166,"keywords":1168,"openalex":1169,"abstract":1171,"title":1173,"doi":1175},{"VOID":1167},"2111904011",{},{"VOID":1170},"W2111904011",{"EN":1172},"\u003Cjats:title>Abstract\u003C\u002Fjats:title>\n          \u003Cjats:p>Osmo- and ionoregulatory abilities were examined in the intertidal grapsid crab, \u003Cjats:italic>Gaetice depressus\u003C\u002Fjats:italic>, transferred from normal seawater (30 ppt) to low (10 ppt) or high (50 ppt) salinities for 2 and 10 days, in addition to animals kept out of water for 2 days. The results of the hemolymph osmotic and ionic status indicate that \u003Cjats:italic>G. depressus\u003C\u002Fjats:italic> is able to adapt for more than 10 days in these salinities and for 2 days under terrestrial conditions. Especially, the free Ca\u003Cjats:sup>2+\u003C\u002Fjats:sup> concentration was relatively maintained compared with concentrations of monovalent ions and osmolality values in 10 and 50 ppt, partly using the complexed calcium (total minus free calcium) as an internal reserve in the hemolymph. In 10 ppt, complexed calcium disappeared from the hemolymph after 10 days, indicating that all the hemolymph calcium was ionized. In 50 ppt, free Ca\u003Cjats:sup>2+\u003C\u002Fjats:sup> was regulated to lower levels than concentrations in the medium, while total calcium increased to higher levels after 2 days. Examination of Na\u003Cjats:sup>+\u003C\u002Fjats:sup>\u002FK\u003Cjats:sup>+\u003C\u002Fjats:sup>-ATPase activity, which has been implicated in ion transport in many crustaceans, revealed that induction of high Na\u003Cjats:sup>+\u003C\u002Fjats:sup>\u002FK\u003Cjats:sup>+\u003C\u002Fjats:sup>-ATPase activity varies among the posterior gills in response to salinities. Ten-ppt salinity induces activity in two of the posterior gills (gill numbers 6 and 7, eight in total), albeit with differing degrees of response. In contrast, 50-ppt salinity stimulates the activity primarily in gill number 8, suggesting that this gill may be associated specifically with ion excretion in \u003Cjats:italic>G. depressus.\u003C\u002Fjats:italic> As a euryhaline amphibious crab, this abundant species around Japan will serve as a model to study the osmotic\u002Fionic regulatory mechanisms which operate in crustaceans.\u003C\u002Fjats:p>",{"EN":1174},"Hemolymph osmotic, ionic status, and branchial Na+\u002FK+-ATPase activity under varying environmental conditions in the intertidal grapsid crab, Gaetice 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Physiol Biochem Zool 1999,72(1):1–18. 10.1086\u002F316643",{"doi":1355},"10.1086\u002F316643",{"id":22,"text":1357,"url":22,"identifiers":1358},"Ahearn GA, Mandal PK, Mandal A: Calcium regulation in crustaceans during the molt cycle: a review and update. Comp Biochem Physiol A Mol Integr Physiol 2004,137(2):247–257. 10.1016\u002Fj.cbpb.2003.10.012",{"doi":1359},"10.1016\u002Fj.cbpb.2003.10.012",{"id":22,"text":1361,"url":22,"identifiers":1362},"Bianchini A, Lauer MM, Nery LE, Colares EP, Monserrat JM, Dos Santos Filho EA: Biochemical and physiological adaptations in the estuarine crab Neohelice granulata during salinity acclimation. Comp Biochem Physiol A Mol Integr Physiol 2008,151(3):423–436. 10.1016\u002Fj.cbpa.2007.12.001",{"doi":1363},"10.1016\u002Fj.cbpa.2007.12.001",{"id":22,"text":1365,"url":22,"identifiers":1366},"Charmantier G, Charmantier-Daures M, Anger K: Ontogeny of osmoregulation in the grapsid crab Armases miersii (Crustacea, Decapoda). Mar Ecol Prog Ser 1998, 164: 285–292.",{"doi":1367},"10.3354\u002Fmeps164285",{"id":22,"text":1369,"url":22,"identifiers":1370},"Charmantier G, Gimenez L, Charmantier-Daures M, Anger K: Ontogeny of osmoremilation, physiological plasticity and larval export strategy in the grapsid crab Chasmagnathus granulata (Crustacea, Decapoda). Mar Ecol Prog Ser 2002, 229: 185–194.",{"doi":1371},"10.3354\u002Fmeps229185",{"id":22,"text":1373,"url":22,"identifiers":1374},"Charmantier G, Charmantier-Daures M, Towle D: Osmotic and ionic regulation in aquatic arthropods. In Osmotic and ionic regulation: cells and animals. Edited by: Evans DH. CRC Press, New York; 2009:165.",{},{"id":22,"text":1376,"url":22,"identifiers":1377},"Dorazio SE, Holliday CW: Gill Na, K-ATPase and osmoregulation in the sand fiddler crab, Uca pugilator. 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J Exp Biol 2007,210(Pt 12):2070–2081.",{"doi":1400},"10.1242\u002Fjeb.004309",{"id":22,"text":1402,"url":22,"identifiers":1403},"Jillette N, Cammack L, Lowenstein M, Henry RP: Down-regulation of activity and expression of three transport-related proteins in the gills of the euryhaline green crab, Carcinus maenas, in response to high salinity acclimation. Comp Biochem Physiol A Mol Integr Physiol 2011,158(2):189–193. 10.1016\u002Fj.cbpa.2010.10.024",{"doi":1404},"10.1016\u002Fj.cbpa.2010.10.024",{"id":22,"text":1406,"url":22,"identifiers":1407},"Kawane M, Wada K, Watanabe K: Comparisons of genetic population structures in four intertidal brachyuran species of contrasting habitat characteristics. Mar Biol 2008,156(2):193–203.",{"doi":1408},"10.1007\u002Fs00227-008-1076-y",{"id":22,"text":1410,"url":22,"identifiers":1411},"Kikuchi T, Tanaka M, Nojima S, Takahashi T: Ecological studies on the pebble crab, Gaetice depressus (de Haan). I. Ecological distribution of the crab and environmental conditions. Publication from the Amakusa Marine Biological Laboratory 1981, 61: 23–34.",{},{"id":22,"text":1413,"url":22,"identifiers":1414},"Lin HC, Su YC, Su SH: A comparative study of osmoregulation in four fiddler crabs (Ocypodidae: Uca). Zool Sci 2002,19(6):643–650. 10.2108\u002Fzsj.19.643",{"doi":1415},"10.2108\u002Fzsj.19.643",{"id":22,"text":1417,"url":22,"identifiers":1418},"Lohrer A, Fukui Y, Wada K, Whitlatch R: Structural complexity and vertical zonation of intertidal crabs, with focus on habitat requirements of the invasive Asian shore crab, Hemigrapsus sanguineus (de Haan). J Exp Mar Biol Ecol 2000,244(2):203–217. 10.1016\u002FS0022-0981(99)00139-2",{"doi":1419},"10.1016\u002FS0022-0981(99)00139-2",{"id":22,"text":1421,"url":22,"identifiers":1422},"Lucu C, Towle DW: Na(+)+K(+)-ATPase in gills of aquatic crustacea. Comp Biochem Physiol A Mol Integr Physiol 2003,135(2):195–214. 10.1016\u002FS1095-6433(03)00064-3",{"doi":1423},"10.1016\u002FS1095-6433(03)00064-3",{"id":22,"text":1425,"url":22,"identifiers":1426},"Luquet CM, Weihrauch D, Senek M, Towle DW: Induction of branchial ion transporter mRNA expression during acclimation to salinity change in the euryhaline crab Chasmagnathus granulatus. J Exp Biol 2005,208(Pt 19):3627–3636.",{"doi":1427},"10.1242\u002Fjeb.01820",{"id":22,"text":1429,"url":22,"identifiers":1430},"McCormick SD: Methods for nonlethal gill biopsy and measurement of Na+, K+-ATPase activity. Can J Fish Aquat Sci 1993,50(3):656–658. 10.1139\u002Ff93-075",{"doi":1431},"10.1139\u002Ff93-075",{"id":22,"text":1433,"url":22,"identifiers":1434},"Morris S: Neuroendocrine regulation of osmoregulation and the evolution of air-breathing in decapod crustaceans. J Exp Biol 2001,204(Pt 5):979–989.",{"doi":1435},"10.1242\u002Fjeb.204.5.979",{"id":22,"text":1437,"url":22,"identifiers":1438},"Morris S: The ecophysiology of air-breathing in crabs with special reference to Gecarcoidea natalis. Comp Biochem Physiol B Biochem Mol Biol 2002,131(4):559–570. 10.1016\u002FS1096-4959(02)00011-8",{"doi":1439},"10.1016\u002FS1096-4959(02)00011-8",{"id":22,"text":1441,"url":22,"identifiers":1442},"Neufeld DS, Cameron JN: Postmoult uptake of calcium by the blue crab (Callinectes sapidus) in water of low Salinity. J Exp Biol 1992, 171: 283–299.",{"doi":1443},"10.1242\u002Fjeb.171.1.283",{"id":22,"text":1445,"url":22,"identifiers":1446},"Onken H, Putzenlechner M: A V-ATPase drives active, electrogenic and Na+−independent Cl- absorption across the gills of Eriocheir sinensis. J Exp Biol 1995,198(Pt 3):767–774.",{"doi":1447},"10.1242\u002Fjeb.198.3.767",{"id":22,"text":1449,"url":22,"identifiers":1450},"Pequeux A: Osmotic regulation in crustaceans. J Crustac Biol 1995,15(1):1–60.",{"doi":1451},"10.2307\u002F1549010",{"id":22,"text":1453,"url":22,"identifiers":1454},"Robertson JD: Ionic regulation in the crab Carcinus maenas (L.) in relation to the moulting cycle. Comp Biochem Physiol 1960,1(3):183–212. 10.1016\u002F0010-406X(60)90023-2",{"doi":1455},"10.1016\u002F0010-406X(60)90023-2",{"id":22,"text":1457,"url":22,"identifiers":1458},"Roer RD, Dillaman RM: Molt-related change in integumental structure and function. In The crustacean integument morphology and biochemistry. Edited by: Horst MN, Freeman JA. CRC Press, Boca Raton; 1993:1–37.",{},{"id":22,"text":1460,"url":22,"identifiers":1461},"Serrano L, Henry RP: Differential expression and induction of two carbonic anhydrase isoforms in the gills of the euryhaline green crab, Carcinus maenas, in response to low salinity. Comp Biochem Physiol Part D Genomics Proteomics 2008,3(2):186–193. 10.1016\u002Fj.cbd.2008.02.003",{"doi":1462},"10.1016\u002Fj.cbd.2008.02.003",{"id":22,"text":1464,"url":22,"identifiers":1465},"Siebers D, Leweck K, Markus H, Winkler A: Sodium regulation in the shore crab Carcinus maenas as related to ambient salinity. Mar Biol 1982,69(1):37–43. 10.1007\u002FBF00396958",{"doi":1466},"10.1007\u002FBF00396958",{"id":22,"text":1468,"url":22,"identifiers":1469},"Towle DW, Weihrauch D: Osmoregulation by gills of euryhaline crabs: molecular analysis of transporters. Am Zool 2001,41(4):770–780. 10.1668\u002F0003-1569(2001)041[0770:OBGOEC]2.0.CO;2",{"doi":1470},"10.1668\u002F0003-1569(2001)041[0770:OBGOEC]2.0.CO;2",{"id":22,"text":1472,"url":22,"identifiers":1473},"Towle DW, Rushton ME, Heidysch D, Magnani JJ, Rose MJ, Amstutz A, Jordan MK, Shearer DW, Wu WS: Sodium\u002Fproton antiporter in the euryhaline crab Carcinus maenas: molecular cloning, expression and tissue distribution. J Exp Biol 1997,200(Pt 6):1003–1014.",{"doi":1474},"10.1242\u002Fjeb.200.6.1003",{"id":22,"text":1476,"url":22,"identifiers":1477},"Towle DW, Henry RP, Terwilliger NB: Microarray-detected changes in gene expression in gills of green crabs (Carcinus maenas) upon dilution of environmental salinity. Comp Biochem Physiol Part D Genomics Proteomics 2011,6(2):115–125. 10.1016\u002Fj.cbd.2010.11.001",{"doi":1478},"10.1016\u002Fj.cbd.2010.11.001",{"id":22,"text":1480,"url":22,"identifiers":1481},"Wheatly MG: Calcium homeostasis in crustacea: the evolving role of branchial, renal, digestive and hypodermal epithelia. J Exp Zool 1999,283(7):620–640. 10.1002\u002F(SICI)1097-010X(19990601)283:7\u003C620::AID-JEZ2>3.0.CO;2-3",{"doi":1482},"10.1002\u002F(SICI)1097-010X(19990601)283:7\u003C620::AID-JEZ2>3.0.CO;2-3",{"id":22,"text":1484,"url":22,"identifiers":1485},"Wheatly MG, Zanotto FP, Hubbard MG: Calcium homeostasis in crustaceans: subcellular Ca dynamics. Comp Biochem Physiol B Biochem Mol Biol 2002,132(1):163–178. 10.1016\u002FS1096-4959(01)00520-6",{"doi":1486},"10.1016\u002FS1096-4959(01)00520-6",{"id":22,"text":1488,"url":22,"identifiers":1489},"Wilder MN, Ikuta K, Atmomarsono M, Hatta T, Komuro K: Changes in osmotic and ionic concentrations in the hemolymph of Macrobrachium rosenbergii exposed to varying salinities and correlation to ionic and crystalline composition of the cuticle. Comp Biochem Phys A 1998,119(4):941–950. 10.1016\u002FS1095-6433(98)00008-7",{"doi":1490},"10.1016\u002FS1095-6433(98)00008-7",{"id":22,"text":1492,"url":22,"identifiers":1493},"Zanders IP, Rojas WE: Transbranchial potentials and ion fluxes across isolated, perfused gills of Uca rapax. Mar Biol 1996,125(2):307–314. 10.1007\u002FBF00346311",{"doi":1494},"10.1007\u002FBF00346311",{"id":22,"text":1496,"url":22,"identifiers":1497},"Zanotto FP, Wheatly MG: Calcium balance in crustaceans: nutritional aspects of physiological regulation. Comp Biochem Physiol A Mol Integr Physiol 2002,133(3):645–660. 10.1016\u002FS1095-6433(02)00202-7",{"doi":1498},"10.1016\u002FS1095-6433(02)00202-7",{"id":1500,"createTime":1501,"updateTime":1502,"relativeEntities":1503,"slug":1504,"properties":1505,"entityType":126,"verifyStatus":234,"verifyTime":1502,"verifyNote":235,"syncStatus":21,"languages":1517,"translateLanguages":22,"viewCount":23,"primaryUrl":1518,"fullTextUrl":22,"authors":1519,"publicationType":180,"publisherRelationship":1606,"citationCount":445,"citationInfo":1641,"publishDate":1643,"publishYear":555,"citationAnalyzeStatus":21,"lastCitationAnalyze":22,"indexDatabases":22,"openAccess":22,"references":1644,"isForceReanalyzing":218},"9fdb4aee-c7e7-4262-85cd-9d806d367dc5","2024-04-21T19:50:43.636+00:00","2024-12-09T22:42:36.677+00:00",[],"Effects-of-dietary-fishmeal-substitution-with-corn-gluten-meal-and-poultry-meal-on-growth-rate-and-flesh-characteristics-of-Chinook-salmon-Oncorhynchus-tshawytscha-",{"mag":1506,"keywords":1508,"openalex":1509,"abstract":1511,"title":1513,"doi":1515},{"VOID":1507},"2972638968",{},{"VOID":1510},"W2972638968",{"EN":1512},"\u003Cjats:title>Abstract\u003C\u002Fjats:title>\n\u003Cjats:p>There is considerable interest in developing diets that maintain growth performance and market appeal for salmon aquaculture while relying less on fishmeal as a major ingredient. Here, we compared growth rate, survival, fat content, tissue colouration and carotenoid levels (astaxanthin) in Chinook salmon (\u003Cjats:italic>Oncorhynchus tshawytscha\u003C\u002Fjats:italic>) fed two diets. The first diet was a typical commercial salmon diet with 59% fishmeal content, while the second diet reduced the fishmeal content to 15% (75% reduction) and substituted 28% corn gluten meal and 16% poultry meal. Over an approximately 14-month growth period, we found no significant difference between fish fed the high fishmeal or low fishmeal diet in either growth rate or survival. Individuals fed the low fishmeal diet did have 25% higher total body fat percentage than those fed the high fishmeal diet. Individuals fed the low fishmeal diet also had flesh that was significantly less red than fish fed the high fishmeal diet. Carotenoid analysis confirmed that the change in tissue colour was the result of reduced astaxanthin levels in salmon fed the low fishmeal diet. Due to the importance of red tissue colour for the market appeal of salmon, the corn gluten and poultry meal diet is not viable for salmon aquaculture in its present formulation, but our results suggest further modifications to the diet that could mitigate this effect.\u003C\u002Fjats:p>",{"EN":1514},"Effects of dietary fishmeal substitution with corn gluten meal and poultry meal on growth rate and flesh characteristics of Chinook salmon (Oncorhynchus tshawytscha)",{"VOID":1516},"10.1007\u002Fs40071-019-00241-3",[914],"http:\u002F\u002Flink.springer.com\u002F10.1007\u002Fs40071-019-00241-3",[1520,1540,1555,1570,1587],{"id":1521,"sortIndex":311,"researcher":22,"roles":1522,"affiliations":1523,"properties":1533},"e7966ea9-d956-4d77-b919-dfbb4f011a9a",[],[1524],{"id":1525,"sortIndex":23,"affiliation":1526,"properties":22},"730f8d8d-7db8-4f6e-9150-ced5a5375ebc",{"id":1527,"createTime":1528,"updateTime":1528,"relativeEntities":1529,"slug":22,"properties":1530,"entityType":43,"verifyStatus":21,"verifyTime":22,"verifyNote":22,"syncStatus":21,"languages":22,"translateLanguages":22,"viewCount":23},"944e1c22-0101-4c84-89c7-27c4754ad8be","2024-01-17T11:40:07.511+00:00",[],{"title":1531},{"VI":1532},"Department of Biology, Western University, London, ON, Canada",{"openalex":1534,"orcid":1536,"title":1538},{"VOID":1535},"A5007234854",{"VOID":1537},"https:\u002F\u002Forcid.org\u002F0000-0001-8499-250X",{"EN":1539},"Bryan D. Neff",{"id":1541,"sortIndex":44,"researcher":22,"roles":1542,"affiliations":1543,"properties":1550},"86327ad3-29bf-4b58-8e21-9d91ef1fc108",[],[1544],{"id":1545,"sortIndex":23,"affiliation":1546,"properties":22},"9eca723e-fdaa-4ea6-8b91-09384144d791",{"id":1527,"createTime":1528,"updateTime":1528,"relativeEntities":1547,"slug":22,"properties":1548,"entityType":43,"verifyStatus":21,"verifyTime":22,"verifyNote":22,"syncStatus":21,"languages":22,"translateLanguages":22,"viewCount":23},[],{"title":1549},{"VI":1532},{"openalex":1551,"title":1553},{"VOID":1552},"A5000131691",{"EN":1554},"Shawn R. Garner",{"id":1556,"sortIndex":23,"researcher":22,"roles":1557,"affiliations":1558,"properties":1565},"dda575fe-394c-4699-a78b-fa1bffa60c39",[],[1559],{"id":1560,"sortIndex":23,"affiliation":1561,"properties":22},"aa3ef3df-f931-4f77-abb9-2cbe9d04dff2",{"id":1527,"createTime":1528,"updateTime":1528,"relativeEntities":1562,"slug":22,"properties":1563,"entityType":43,"verifyStatus":21,"verifyTime":22,"verifyNote":22,"syncStatus":21,"languages":22,"translateLanguages":22,"viewCount":23},[],{"title":1564},{"VI":1532},{"openalex":1566,"title":1568},{"VOID":1567},"A5052344831",{"EN":1569},"Katarina H. Doughty",{"id":1571,"sortIndex":169,"researcher":22,"roles":1572,"affiliations":1573,"properties":1580},"d3af6487-8b76-46c2-9899-13b92584b380",[],[1574],{"id":1575,"sortIndex":23,"affiliation":1576,"properties":22},"c2f6ad97-dd7e-420f-81a3-6218a4f213b9",{"id":1527,"createTime":1528,"updateTime":1528,"relativeEntities":1577,"slug":22,"properties":1578,"entityType":43,"verifyStatus":21,"verifyTime":22,"verifyNote":22,"syncStatus":21,"languages":22,"translateLanguages":22,"viewCount":23},[],{"title":1579},{"VI":1532},{"openalex":1581,"orcid":1583,"title":1585},{"VOID":1582},"A5001826100",{"VOID":1584},"https:\u002F\u002Forcid.org\u002F0000-0003-1209-3200",{"EN":1586},"Mark A. Bernards",{"id":1588,"sortIndex":464,"researcher":22,"roles":1589,"affiliations":1590,"properties":1601},"a163891f-6539-4bb0-bbc6-d500f2d87c33",[],[1591],{"id":1592,"sortIndex":23,"affiliation":1593,"properties":22},"a94a1219-6fe9-4365-8624-f377a62d5984",{"id":1594,"createTime":1595,"updateTime":1595,"relativeEntities":1596,"slug":1597,"properties":1598,"entityType":43,"verifyStatus":21,"verifyTime":22,"verifyNote":22,"syncStatus":21,"languages":22,"translateLanguages":22,"viewCount":23},"13360a98-1aaa-4c90-aaa0-c54ce1f872b7","2024-04-21T19:50:43.683+00:00",[],"Yellow-Island-Aquaculture-Heriot-Bay-BC-Canada",{"title":1599},{"EN":1600},"Yellow Island Aquaculture, Heriot Bay, BC, Canada",{"openalex":1602,"title":1604},{"VOID":1603},"A5052269545",{"EN":1605},"John Heath",{"url":22,"publisher":1607,"properties":1636},{"id":6,"createTime":7,"updateTime":8,"relativeEntities":1608,"slug":10,"properties":1609,"entityType":20,"verifyStatus":21,"verifyTime":22,"verifyNote":22,"syncStatus":21,"languages":22,"translateLanguages":22,"viewCount":23,"subjectFields":1614,"manageAffiliations":1615,"indexDatabases":1616,"url":22,"thumbnailPath":22,"statistic":1631,"gsStatistic":22,"type":108,"analyzePriority":22},[],{"issn":1610,"eissn":1611,"title":1612,"url":1613},{"VOID":13},{"VOID":15},{"EN":17},{"VOID":19},[],[],[1617,1624],{"id":58,"indexDatabase":1618,"url":22,"indexYears":22,"academicFieldIds":1623,"indexDatabaseRanking":22},{"id":60,"createTime":61,"updateTime":62,"relativeEntities":1619,"label":1620,"description":1621,"key":69,"publicationTags":1622,"standard":22},[],{"EN":65,"VI":65},{"VI":67,"EN":68},[71,72],[74],{"id":76,"indexDatabase":1625,"url":89,"indexYears":90,"academicFieldIds":1630,"indexDatabaseRanking":93},{"id":78,"createTime":79,"updateTime":80,"relativeEntities":1626,"label":1627,"description":1628,"key":86,"publicationTags":1629,"standard":22},[],{"EN":83,"VI":83},{"EN":83,"VI":85},[88],[92],{"impactFactor":23,"impactFactorByYear":1632,"i10Index":23,"i10IndexLast5Year":23,"totalPublication":96,"totalPublicationByYear":1633,"totalCitation":23,"totalCitationByYear":1634,"totalCitationPerPublication":23,"totalCitationPerPublicationByYear":1635,"hindexLast5Year":23,"hindex":23},{},{"2012":98,"2013":99,"2014":100,"2015":101,"2016":102,"2017":103,"2018":104,"2019":105},{},{},{"volume":1637,"pages":1638,"issue":1640},{"VOID":551},{"VOID":1639},"325-334",{"VOID":1344},{"total":445,"publishYear":22,"statisticByYear":1642},{"2021":99,"2023":44},"2019-12-01",[1645,1648,1652,1656,1659,1663,1667,1671,1675,1679,1683,1687,1691,1695,1699,1703,1707,1711,1714,1717,1721,1725,1729,1733,1737,1741,1745,1749],{"id":22,"text":1646,"url":22,"identifiers":1647},"Anderson S (2001) Salmon color and the consumer. In: Johnston RS, Shriver AL (eds) Proceedings of the tenth biennial conference of the International Institute of Fisheries economics and trade presentations. Oregon State University, Corvallis, pp 1–3",{},{"id":22,"text":1649,"url":22,"identifiers":1650},"Bjerkeng B, Refstie S, Fjalestad KT, Storebakken T, Rødbotten M, Roem AJ (1997) Quality parameters of the flesh of Atlantic salmon (Salmo salar) as affected by dietary fat content and full-fat soybean meal as a partial substitute for fish meal in the diet. Aquaculture 157:297–309",{"doi":1651},"10.1016\u002FS0044-8486(97)00162-2",{"id":22,"text":1653,"url":22,"identifiers":1654},"Burr GS, Wolters WR, Barrows FT, Hardy RW (2012) Replacing fishmeal with blends of alternative proteins on growth performance of rainbow trout (Oncorhynchus mykiss), and early or late stage juvenile Atlantic salmon (Salmo salar). Aquaculture 334–337:110–116",{"doi":1655},"10.1016\u002Fj.aquaculture.2011.12.044",{"id":22,"text":1657,"url":22,"identifiers":1658},"De Silva SS, Anderson TA (1994) Fish nutrition in aquaculture. Springer, Berlin",{},{"id":22,"text":1660,"url":22,"identifiers":1661},"Fowler LG (1991) Poultry by-product meal as a dietary protein source in fall chinook salmon diets. Aquaculture 99:309–321",{"doi":1662},"10.1016\u002F0044-8486(91)90251-2",{"id":22,"text":1664,"url":22,"identifiers":1665},"Furr HC, Clark RM (1997) Intestinal absorption and tissue distribution of carotenoids. J Nutr Biochem 8:364–377",{"doi":1666},"10.1016\u002FS0955-2863(97)00060-0",{"id":22,"text":1668,"url":22,"identifiers":1669},"Garner SR, Neff BD, Bernards MA (2010) Dietary carotenoid levels affect carotenoid and retinoid allocation in female Chinook salmon Oncorhynchus tshawytscha. J Fish Biol 76:1474–1490",{"doi":1670},"10.1111\u002Fj.1095-8649.2010.02579.x",{"id":22,"text":1672,"url":22,"identifiers":1673},"Gatlin DM, Barrows FT, Brown P, Dabrowski K, Gaylord TG, Hardy RW, Herman E, Hu G, Krogdahl Å, Nelson R, Overturf K, Rust M, Sealey W, Skonberg D, Souza EJ, Stone D, Wilson R, Wurtele E (2007) Expanding the utilization of sustainable plant products in aquafeeds: a review. Aquac Res 38:551–579",{"doi":1674},"10.1111\u002Fj.1365-2109.2007.01704.x",{"id":22,"text":1676,"url":22,"identifiers":1677},"Goodwin TW (1986) Metabolism, nutrition, and function of carotenoids. Annu Rev Nutr 6:273–297",{"doi":1678},"10.1146\u002Fannurev.nu.06.070186.001421",{"id":22,"text":1680,"url":22,"identifiers":1681},"Hatlen B, Jakobsen J-V, Crampton V, Alm M, Langmyhr E, Espe M, Hevrøy EM, Torstensen BE, Liland N, Waagbø R (2015) Growth, feed utilization and endocrine responses in Atlantic salmon (Salmo salar) fed diets added poultry by-product meal and blood meal in combination with poultry oil. Aquac Nutr 21:714–725",{"doi":1682},"10.1111\u002Fanu.12194",{"id":22,"text":1684,"url":22,"identifiers":1685},"Lu F, Haga Y, Satoh S (2015) Effects of replacing fish meal with rendered animal protein and plant protein sources on growth response, biological indices, and amino acid availability for rainbow trout Oncorhynchus mykiss. Fish Sci 81:95–105",{"doi":1686},"10.1007\u002Fs12562-014-0818-7",{"id":22,"text":1688,"url":22,"identifiers":1689},"Mambrini M, Roem AJ, Carvedi JP, Lalles JP, Kaushik SJ (1999) Effects of replacing fish meal with soy protein concentrate and of dl-methionine supplementation in high-energy, extruded diets on the growth and nutrient utilization of rainbow trout, Oncorhynchus mykiss. J Anim Sci 77:2990–2999",{"doi":1690},"10.2527\u002F1999.77112990x",{"id":22,"text":1692,"url":22,"identifiers":1693},"Matsuno T (1991) Xanthophylls as precursors of retinoids. Pure Appl Chem 63:81–88",{"doi":1694},"10.1351\u002Fpac199163010081",{"id":22,"text":1696,"url":22,"identifiers":1697},"Mente E, Deguara S, Santos M, Houlihan D (2003) White muscle free amino acid concentrations following feeding a maize gluten dietary protein in Atlantic salmon (Salmo salar L.). Aquaculture 225:133–147",{"doi":1698},"10.1016\u002FS0044-8486(03)00285-0",{"id":22,"text":1700,"url":22,"identifiers":1701},"Moreno JA, Díaz-Gómez J, Nogareda C, Angulo E, Sandmann G, Portero-Otin M, Serrano JCE, Twyman RM, Capell T, Zhu C, Christou P (2016) The distribution of carotenoids in hens fed on biofortified maize is influenced by feed composition, absorption, resource allocation and storage. Sci Rep 6:35346",{"doi":1702},"10.1038\u002Fsrep35346",{"id":22,"text":1704,"url":22,"identifiers":1705},"Moros EE, Darnoko D, Cheryan M, Perkins EG, Jerrell J (2002) Analysis of xanthophylls in corn by HPLC. J Agric Food Chem 50:5787–5790",{"doi":1706},"10.1021\u002Fjf020109l",{"id":22,"text":1708,"url":22,"identifiers":1709},"Mundheim H, Aksnes A, Hope B (2004) Growth, feed efficiency and digestibility in salmon (Salmo salar L.) fed different dietary proportions of vegetable protein sources in combination with two fish meal qualities. Aquaculture 237:315–331",{"doi":1710},"10.1016\u002Fj.aquaculture.2004.03.011",{"id":22,"text":1712,"url":22,"identifiers":1713},"National Research Council (1993) Nutrient requirements of fish. The National Academies Press, Washington, DC",{},{"id":22,"text":1715,"url":22,"identifiers":1716},"National Research Council (2011) Nutrient requirements of fish and shrimp. The National Academies Press, Washington, DC",{},{"id":22,"text":1718,"url":22,"identifiers":1719},"Olsen RE, Baker RTM (2006) Lutein does not influence flesh astaxanthin pigmentation in the Atlantic salmon (Salmo salar L.). Aquaculture 258:558–564",{"doi":1720},"10.1016\u002Fj.aquaculture.2006.03.031",{"id":22,"text":1722,"url":22,"identifiers":1723},"Parés-Sierra G, Durazo E, Ponce MA, Badillo D, Correa-Reyes G, Viana MT (2014) Partial to total replacement of fishmeal by poultry by-product meal in diets for juvenile rainbow trout (Oncorhynchus mykiss) and their effect on fatty acids from muscle tissue and the time required to retrieve the effect. Aquac Res 45:1459–1469",{"doi":1724},"10.1111\u002Fare.12092",{"id":22,"text":1726,"url":22,"identifiers":1727},"Park H, Flores RA, Johnson LA (1997) Preparation of fish feed ingredients: reduction of carotenoids in corn gluten meal. J Agric Food Chem 45:2088–2092",{"doi":1728},"10.1021\u002Fjf960972j",{"id":22,"text":1730,"url":22,"identifiers":1731},"Saez PJ, Abdel-Aal E-SM, Bureau DP (2014) Reduction of carotenoids in corn gluten meal: effects on growth performance and muscle pigmentation of rainbow trout (Oncorhynchus mykiss). Can J Anim Sci 95:79–92",{"doi":1732},"10.4141\u002Fcjas-2014-108",{"id":22,"text":1734,"url":22,"identifiers":1735},"Saez PJ, Abdel-Aal E-SM, Bureau DP (2016) Feeding increasing levels of corn gluten meal induces suboptimal muscle pigmentation of rainbow trout (Oncorhynchus mykiss). Aquac Res 47:1972–1983",{"doi":1736},"10.1111\u002Fare.12653",{"id":22,"text":1738,"url":22,"identifiers":1739},"Sargent J, Bell G, McEvoy L, Tocher D, Estevez A (1999) Recent developments in the essential fatty acid nutrition of fish. Aquaculture 177:191–199",{"doi":1740},"10.1016\u002FS0044-8486(99)00083-6",{"id":22,"text":1742,"url":22,"identifiers":1743},"Sealey WM, Hardy RW, Barrows FT, Pan Q, Stone DAJ (2011) Evaluation of 100% fish meal substitution with chicken concentrate, protein poultry by-product blend, and chicken and egg concentrate on growth and disease resistance of juvenile rainbow trout, Oncorhynchus mykiss. J World Aquac Soc 42:46–55",{"doi":1744},"10.1111\u002Fj.1749-7345.2010.00442.x",{"id":22,"text":1746,"url":22,"identifiers":1747},"Steffens W (1994) Replacing fish meal with poultry by-product meal in diets for rainbow trout, Oncorhynchus mykiss. Aquaculture 124:27–34",{"doi":1748},"10.1016\u002F0044-8486(94)90351-4",{"id":22,"text":1750,"url":22,"identifiers":1751},"Torrissen O, Hardy R, Shearer K (1989) Pigmentation of salmonids–carotenoid deposition and metabolism. CRC Crit Rev Aquat Sci 1:209–225",{},{"id":1753,"createTime":1754,"updateTime":1755,"relativeEntities":1756,"slug":1757,"properties":1758,"entityType":126,"verifyStatus":234,"verifyTime":1755,"verifyNote":235,"syncStatus":21,"languages":22,"translateLanguages":22,"viewCount":23,"primaryUrl":1767,"fullTextUrl":22,"authors":1768,"publicationType":180,"publisherRelationship":1830,"citationCount":22,"citationInfo":22,"publishDate":1865,"publishYear":1866,"citationAnalyzeStatus":21,"lastCitationAnalyze":22,"indexDatabases":22,"openAccess":22,"references":22,"isForceReanalyzing":218},"db24bce5-cc5a-4d88-8e37-146f48a3e2bb","2023-12-13T13:58:41.652+00:00","2024-12-23T22:30:30.529+00:00",[],"Growth-performance-feed-utilisation-and-biological-indices-of-Tra-catfish-Pangasianodon-hypophthalmus-cultured-in-net-cages-in-pond-fed-diets-based-on-locally-available-feed-resources",{"references":1759,"abstract":1761,"title":1763,"doi":1765},{"VOID":1760},"AOAC (1997) Animal feeds. Chapter 4. In: Cunniff PA (ed) Official methods of analysis vol 1. Association of Official Analytical Chemists International. AOAC, Arlington, pp VI, 1102\nBellinger EG, Sigee DC (2010) Introduction to freshwater algae, in freshwater algae: identification and use as bioindicators. John Wiley & Sons, Ltd, Chichester, UK, pp 1–285. doi:10.1002\u002F9780470689554.ch1\nBui TM, Lam PT, Ingram BA, Thuy NTT, Gooley GJ, Hao NV, Phuong NT, De Silva SS (2010) Seed production practices of striped catfish (Pangasianodon hypophthalmus) in the Mekong Delta region, Vietnam. Aquaculture 306:92–100\nCacot P, Pariselle A (1999) Description of the sexual cycle related to the environment and set up of the artificial propagation in Pangasius bocourti (Sauvage 1880) and Pangasius hypophthalmus (Sauvage 1878) reared in floating cages and in ponds in the Mekong Delta. In: Legendre M, Pariselle A (eds) The biological diversity and aquaculture of Clariid and Pangasiid catfishes in South East Asia. Proceedings of the mid-term workshop of the ‘Catfish Asia Project’, 11–15 May 1998. Cantho, Vietnam, pp 71–89\nDa CT, Hung LT, Berg H, Lindberg JE, Lundh T (2011) Evaluation of potential feed sources, and technical and economic considerations of small-scale commercial striped catfish (Pangasius hypothalamus) pond farming systems in the Mekong Delta of Vietnam. Aquac Res 44:427–438. doi:10.1111\u002Fj.1365-2109.2011.03048.x\nDa CT, Lundh T, Lindberg JE (2012) Evaluation of local feed resources as alternatives to fish meal in terms of growth performance, feed utilisation and biological indices of striped catfish (Pangasianodon hypophthalmus) fingerlings. Aquaculture 364–365:150–156\nDe Silva SS, Phuong NT (2011) Striped catfish farming in the Mekong Delta, Vietnam: a tumultuous path to a global success. Rev Aquac 3:45–73\nDeng J, Zhang X, Bi B, Kong L, Kang B (2011) Dietary protein requirement of juvenile Asian red-tailed catfish (Hemibagrus wyckioides). Anim Feed Sci Technol 170:231–238\nEdwards P, Tuan LA, Allan GL (2004) A survey of marine trash fish and fish meal as aquaculture feed ingredients in Vietnam. Australian Centre for International Agricultural Research. Working Paper No. 57, pp 1–56\nFagbenro OA (2004) Soybean meal replacement by roquette (Eruca sativa Miller) seed meal as protein feedstuff in diets for African Catfish (Clarias gariepinus, Burchell 1822), fingerlings. Aquac Res 35:917–923\nFAO (2010) Fisheries and Aquaculture. Food and Agriculture Organization (FAO) of United Nations. http:\u002F\u002Fwww.eoearth.org\u002Farticle\u002FFood_and_Agriculture_Organization_(FAO). Accessed 19 June 2011\nHalls A, Johns M (2013) Assessment of the vulnerability of the Mekong Delta Pangasius catfish industry to development and climate change in the Lower Mekong Basin. Report prepared for the Sustainable Fisheries Partnership\nHernández MD, Martínez FJ, Jover M, García García B (2007) Effects of partial replacement of fish meal by soybean meal in sharpsnout seabream (Diplodus puntazzo) diet. Aquaculture 263:159–167\nHue KT, Van DTT, Ledin I, Spörndly E, Wredle E (2010) Effect of feeding fresh, wilted and sun-dried foliage from cassava (Manihot esculenta Crantz) on the performance of lambs and their intake of hydrogen cyanide. Livest Sci 131:155–161\nHung LT, Liem PT, Tu HT, Mariojouls C (2002) Comparing growth and protein requirements for fingerlings of three catfish of the Mekong River (Pangasius bocourti, Pangagasius hypothalmus and Pangasius conchophilus). J Aquac Trop 17:325–335\nHung LT, Suhenda N, Slembrouck J, Lazard J, Moreau Y (2003) Comparison of starch utilization in fingerlings of two Asian catfishes from the Mekong River (Pangasius bocourti Sauvage, 1880, Pangasius hypophthalmus Sauvage, 1878). Aquac Nutr 9:215–222\nHung LT, Suhenda N, Slembrouck J, Lazard J, Moreau Y (2004) Comparison of dietary protein and energy utilization in three Asian catfishes (Pangasius bocourti, P. hypophthalmus and P. djambal). Aquac Nutr 10:317–326\nHung LT, Truc LTT, Huy HPV (2007) Case study on the use of farm-made feeds and commercially formulated pellets for pangasiid catfish culture in the Mekong Delta, Viet Nam: Study and analysis of feeds and fertilizers for sustainable aquaculture development. Food and Agriculture Organization of United Nattion—FAO, Fisheries Technical Paper No. 497, pp 363–377\nIBM SPSS STATISTIC (2011) IBM SPSS STATISTIC program, version 19 statistical software packages. IBM Corporation, New York\nJackson AJ, Capper BS (1982) Investigations into the requirements of the tilapia (Sarotherodon mossambicus) for dietary methionine, lysine and arginine in semi-synthetic diets. Aquaculture 29:289–297\nKader MA, Koshio S, Ishikawa M, Yokoyama S, Bulbul M (2010) Supplemental effects of some crude ingredients in improving nutritive values of low fishmeal diets for red sea bream, Pagrus major. Aquaculture 308:136–144\nLoc V, Bush S, Sinh L, Khiem N (2010) High and low value fish chains in the Mekong Delta: challenges for livelihoods and governance. Environ Dev Sustain 12:889–908\nMamat NZ, Alfaro AC (2014) Evaluation of microalgal and formulated diets for the culture of the New Zealand pipi clam Paphies australis. Int Aquat Res 6:57. doi:10.1007\u002Fs40071-014-0057-7\nNaylor RL, Hardy RW, Bureau DP, Chiu A, Elliott M (2009) Feeding aquaculture in an era of finite resources. Proc Natl Acad Sci USA 106:15103–15110\nNguyen THL, Ngoan LD, Bosch G, Verstegen MWA, Hendriks WH (2012) Ileal and total tract apparent crude protein and amino acid digestibility of ensiled and dried cassava leaves and sweet potato vines in growing pigs. Anim Feed Sci Technol 172:171–179\nNordrum S, Bakke-McKellep AM, Krogdahl Å, Buddington RK (2000) Effects of soybean meal and salinity on intestinal transport of nutrients in Atlantic salmon (Salmo salar L.) and rainbow trout (Oncorhynchus mykiss). Comp Biochem Physiol Part B 125:317–335\nNyina-wamwiza L, Wathelet B, Kestemont P (2007) Potential of local agricultural by-products for the rearing of African catfish (Clarias gariepinus) in Rwanda: effects on growth, feed utilization and body composition. Aquac Res 38:206–214\nPeres H, Oliva-Teles A (2008) Lysine requirement and efficiency of lysine utilization in turbot (Scophthalmus maximus) juveniles. Aquaculture 275:283–290\nPhan TL, Tam BM, Thuy NTT, Geoff GJ, Brett IA, Hao NV, Phuong NT, Silva SSD (2009) Current status of farming practices of striped catfish, Pangasianodon hypophthalmus in the Mekong Delta, Vietnam. Aquaculture 296:227–236\nPhuc BHN, Lindberg JE (2000) Ileal and total tract digestibility in growing pigs given cassava root meal diets with inclusion of cassava leaves, leucaena leaves and groundnut foliage. Br Soc Anim Sci 17:301–308\nPhuc BHN, Lindberg JE (2001) Ileal apparent digestibility of amino acids in growing pigs given a cassava root meal diet with inclusion of cassava leaves, leucaena leaves and groundnut foliage. Anim Sci 72:511–517\nPhumee P, Wei WY, Ramachandran S, Hashim R (2011) Evaluation of soybean meal in the formulated diets for juvenile Pangasianodon hypophthalmus (Sauvage, 1878). Aquac Nutr 17:214–222\nPhuong NT (1998) Pangasius catfish cage aquaculture in the Mekong Delta, Vietnam: current status and study for feeding improvement. College of Aquaculture and Fisheries, Can Tho University, Vietnam, Doctoral thesis no. 1999 (Library of Can Tho University), p 29\nPhuong NT, Sinh LX, Thinh NQ (2007) Economics of aquaculture feeding practices: Vietnam. FAO Fish Tech Pap Rome 505:183–205\nPhuong NT, Ut VN, Tung VT, Hang NTT, Lien NTK, Oanh DTH, Huong DTT, Morales EJ (2010) Water quality monitoring in striped catfish (Pangasianodom hypophthalmus) farms in the Mekong Delta, Vietnam. College of Aquacultrue and Fisheries, Can Tho University, Vietnam, Sustainable Fisheries Partnership, pp 1–19. http:\u002F\u002Fmedia.sustainablefish.org\u002FFinal%20report_Water%20Quality2009_final.pdf. Accessed 29 May 2012\nSchwarz FJ, Kirchgessner M (1988) Amino acid composition of carp (Cyprinus carpio L.) with varying protein and energy supplies. Aquaculture 72:307–317\nStirling HP (1985) Chemical and biological methods of water analysis for aquaculturists. Institute of Aquaculture, University of Stirling, Stirling, p 117\nSuthers IM, Rissik D (2008) Plankton: a guide to their ecology and monitoring for water quality. CSIRO Publishing, Collingwood, pp 1–273\nTCVN 5942 (1995) National standard (TCVN 5942-1995). Ministry of Fisheries, Hanoi. Sector Standard (TCVN 5942)\nTram NDQ, Ngoan LD, Hung LT, Lindberg JE (2011) A comparative study on the apparent digestibility of selected feedstuffs in Hybride catfish (Claria macrocephalus × Clarias gariepinus) and Nile tilapia (Oreochromis niloticus). Aquac Nutr 17:636–643\nVan Soest PJ, Robertson JB, Lewis BA (1991) Method of dietary fiber, neutral detergent fiber, and nonstarch polysaccharides in relation to animal nutrition. J Dairy Sci 74:3583–4597\nVázquez-Ortiz FA, Caire G, Huguere-Ciapara I, Hernández G (1995) High-performance liquid chromatographic determination of free amino acid in shrimp. J Liq Chromatogr 18:2059–2068\nWilson RP (1989) Amino acids and proteins. In: Halver JE (ed) Fish nutrition, 2nd edn. Academic Press, New York, pp 111–151\nWilson RP, Poe WE, Robinson EH (1980) Leucine, isoleucine, valine and histidine requirements of fingerling channel catfish. J Nutr 110:6273",{"EN":1762},"The feeding experiment was conducted to evaluate the efficacy of locally available feed resources for Tra catfish (Pangasianodon hypophthalmus) cultured a series of 21 hapa net cages installed in the earthen pond during a 4-month period. The reference diet contained fish meal as the main crude protein (CP) source, whilst in the seven test diets 20–100 % of the fish meal CP was replaced with CP from local feed ingredients: groundnut cake (GNC), cassava leaf meal (CSLM), sweet potato leaf meal (SPLM), soybean meal (SBM), golden apple snail meal (GASM) and shrimp head meal. There were differences (p \u003C 0.05) among diets in final body weight, total weight gain, daily weight gain, specific growth rate, viscera-somatic weight (VSI%), hepato-somatic index (HIS%) and intra-peritoneal fat (IPF%). The respective values for the shrimp head meal diet were numerically highest, followed in descending order by the reference, GASM, GNC, SPLM, CSLM and SBM diet. Food conversion ratio, fish survival rate, total feed intake, feed utilisation, fish fillet and kidney proportions did not differ among the reference and test diets (p > 0.05). However, the viscera-somatic, hepato-somatic, kidney and intra-peritoneal fat indices differed among treatments (p \u003C 0.05). These data show that fish meal protein can be replaced with protein from locally available plant and animal feed ingredient resources in feed cultured in net cages in pond for Tra catfish fingerlings in effectively compromising growth performance, feed utilisation or carcass traits of fish.",{"EN":1764},"Growth performance, feed utilisation and biological indices of Tra catfish (Pangasianodon hypophthalmus) cultured in net cages in pond fed diets based on locally available feed 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