Search results for "Crassostrea gigas"

showing 6 items of 6 documents

Multi-isotopic and trace element evidence against different formation pathways for oyster microstructures

2021

Geochimica et cosmochimica acta 308, 326-352 (2021). doi:10.1016/j.gca.2021.06.012

BiomineralizationRARE-EARTH-ELEMENTSOysternitrogen isotopes550010504 meteorology & atmospheric sciencesPaleoclimateXRF010502 geochemistry & geophysicsSulfur isotopes01 natural sciencesMineralization (biology)Clumped isotopesMg/Cachemistry.chemical_compoundSclerochronologyddc:550CALCIFICATION RATECRASSOSTREA-GIGASCalcitebiologyStable isotope ratioOysterDistribution coefficientBivalveCalcitetrace elementOxygen isotope ratio cyclePacific oysterSTABLE-ISOTOPEStable isotopeIsotopes of nitrogenChemistryNORTH-SEASEMMECHANICAL CHARACTERISTICSmicrostructureCrassostrea gigas [Portuguese oyster]Ostreidae [oysters]MineralogyGeochemistry and Petrologybiology.animalClumpcd isotopes0105 earth and related environmental sciencesTrace elementARAGONITIC BIVALVE SHELLSbiology.organism_classificationBivalviachemistryTEMPERATURE-DEPENDENCEFORAMINIFERAL CALCITECrassostrea gigasHIGH-RESOLUTION
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Experimental and natural cathodoluminescence in the shell of Crassostrea gigas from Thau lagoon (France): ecological and environmental implications.

2006

We present a cathodoluminescence (CL) study of growth layer deposition in the shell of the oyster Crassostrea gigas. CL is based on the physical properties of lattice-bound manganese (Mn2+), which is the main activator in calcium carbonate. Our study involved chemical marking by immersing individuals in seawater to which manganese chloride had been added, and subsequent reading of the shell with CL microscopy coupled with numeric treatment of microphotographs; CL emission was analyzed using a scanning electron microscope coupled to a spectrometer. Since the marking did not harm the oysters, repeated markings were possible, allowing validation of the inferences made from analysis of the shel…

0106 biological sciencesOysterBiogeochemical cycleCarbonate biomineraliation010504 meteorology & atmospheric sciencesCathodoluminescenceCrassostrea gigas [Portuguese oyster]CathodoluminescenceAquatic Science01 natural sciencesShell growthchemistry.chemical_compoundbiology.animal14. Life underwater[SDV.IB.BIO]Life Sciences [q-bio]/Bioengineering/BiomaterialsEcology Evolution Behavior and SystematicsComputingMilieux_MISCELLANEOUS0105 earth and related environmental sciencesEcologybiologyEcologyOyster010604 marine biology & hydrobiologyMediterranean lagoonManganese markingBivalviabiology.organism_classification[ SDV.IB.BIO ] Life Sciences [q-bio]/Bioengineering/Biomaterials[SDV.IB.BIO] Life Sciences [q-bio]/Bioengineering/BiomaterialsOstreidaeCarbonate biomirealizationchemistryCrassostreaCarbonateSeawater
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Experiences of integrated mariculture in a southern Tyrrhenian area (Mediterranean Sea)

1999

To ascertain the potential for exploiting marine areas for mariculture, data on the cultivation of molluscs and fish in the open sea of the southern Tyrrhenian were collected from May 1994 to June 1995. The aims of this integrated study were to test simple breeding methods for molluscs and fish, to apply these to the practices employed by local fishermen and to experiment with the use of a cage system requiring a low level of investment. Crassostrea gigas (Thunberg) and Mytilus galloprovincialis (Lamarck) were cultivated on submerged long lines around cages used for cultivating Seriola dumerili (Risso) and Diplodus puntazzo (Cetti). S. dumerili specimens were placed in two cages and fed wit…

Settore BIO/07 - Ecologiabivalves fish Crassostrea gigas Mytilus galloprovincialis Seriola dumerili Diplodus puntazzo aquaculture
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Growth and reproductive simulation of candidate shellfish species at fish cages in the Southern Mediterranean: Dynamic Energy Budget (DEB) modelling …

2012

Abstract A Dynamic Energy Budget (DEB) model is used to simulate growth and reproduction of the shellfish Mytilus galloprovincialis and Crassostrea gigas in an integrated multi-trophic aquaculture (IMTA) farm scenario situated in the Southern Mediterranean (the Gulf of Castellammare, Sicily). We modelled the effect of primary production enrichment at fish cages on shellfish growth and life history traits using 4 years-hourly temperature data (01 January 2006–31 December 2009) at a depth of 1 m. Outputs of the DEB simulations were: the maximum theoretical total shell length of shellfish, the potential reproductive outputs and the mean annual von Bertalanffy growth rate. There was a mean incr…

Settore BIO/07 - EcologiaOysterbiologybusiness.industryDynamic energy budgetAquatic Sciencebiology.organism_classificationMytilusIMTA DEB model Chlorophyll a Mytilus galloprovincialis Crassostrea gigas Mediterranean SeaFishery/dk/atira/pure/sustainabledevelopmentgoals/life_below_waterMediterranean seaOceanographyAquaculturebiology.animalCrassostreaSDG 14 - Life Below WaterbusinessIntegrated multi-trophic aquacultureShellfish
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Data from: Phylogenomics of Lophotrochozoa with consideration of systematic error

2016

Phylogenomic studies have improved understanding of deep metazoan phylogeny and show promise for resolving incongruences among analyses based on limited numbers of loci. One region of the animal tree that has been especially difficult to resolve, even with phylogenomic approaches, is relationships within Lophotrochozoa (the animal clade that includes molluscs, annelids, and flatworms among others). Lack of resolution in phylogenomic analyses could be due to insufficient phylogenetic signal, limitations in taxon and/or gene sampling, or systematic error. Here, we investigated why lophotrochozoan phylogeny has been such a difficult question to answer by identifying and reducing sources of sys…

Helobdella robustaGlycera dibranchiataMytilus edulisAnnelidaEntalina tetragonaLeptochiton asellusCerebratulus marginatusLoxosomella cf. viviparaGraptacme eboreaLineus longissimusmedicine and health careClymenella torquataRuditapes philippinarumNucella lapillusHaliotis rufescenslong branch attractionPlatyzoaBarentsia gracilisPriapulus caudatusLineus ruberAlitta virenssaturationProchaetoderma californicumPinctada fucataSchistosoma mansoniLife sciencesPolyzoaCephalothrix hongkongensisRhyssoplax olivaceusLoxosoma pectinaricolaPhascolosoma agassiziiAdineta vagaDrosophila melanogasterEntoproctaBugula neritinaPhoronis vancouverensisMedicineNovocrania anomalaVillosa lienosaDaphnia pulexSagitta sp.Pectinaria gouldiiSymbion americanusNuculana pernulaSepia esculentaEnucula tenuisSolemya velumLineus lacteusTubulanus polymorphus-StruckGnathostomula paradoxaBoccardia proboscideaMacellomenia schanderiLaevipilina hyalinaTubulanus polymorphus-HalanychBryozoaPomatoceros lamarckiiSepioteuthis lessonianaParanemertes peregrinaMalacobdella grossaHemithiris psittaceaLeptochiton rugatusTrochozoaBrachionus plicatilisSpathoderma clenchiLaqueus californicusPatella vulgataLottia giganteaCrepidula fornicataPhoronidaAplysia californicaGlottidia pyramidataPhoronis psammophilaSchmidtea mediterraneaAlexandromenia crassaBrachiopodaMegadasys sp.Octopus vulgarisCapitella teletaNeomenia carinatacompositional heterogeneityNemerteaPhenacolepas pulchellaGadila tolmieiMolluscaMacrodasys sp.Crassostrea gigasPedicellina cernuaTaenia pisiformisDosidicus gigasCephalothrix linearisSpiralia
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Data from: Phylogenomics of Lophotrochozoa with consideration of systematic error

2021

Phylogenomic studies have improved understanding of deep metazoan phylogeny and show promise for resolving incongruences among analyses based on limited numbers of loci. One region of the animal tree that has been especially difficult to resolve, even with phylogenomic approaches, is relationships within Lophotrochozoa (the animal clade that includes molluscs, annelids, and flatworms among others). Lack of resolution in phylogenomic analyses could be due to insufficient phylogenetic signal, limitations in taxon and/or gene sampling, or systematic error. Here, we investigated why lophotrochozoan phylogeny has been such a difficult question to answer by identifying and reducing sources of sys…

Helobdella robustaGlycera dibranchiataMytilus edulisAnnelidaEntalina tetragonaLeptochiton asellusCerebratulus marginatusLoxosomella cf. viviparaGraptacme eboreaLineus longissimusmedicine and health careClymenella torquataRuditapes philippinarumNucella lapillusHaliotis rufescenslong branch attractionPlatyzoaBarentsia gracilisPriapulus caudatusLineus ruberAlitta virenssaturationProchaetoderma californicumLife SciencesPinctada fucataSchistosoma mansoniPolyzoaCephalothrix hongkongensisRhyssoplax olivaceusLoxosoma pectinaricolaPhascolosoma agassiziiAdineta vagaDrosophila melanogasterEntoproctaBugula neritinaPhoronis vancouverensisMedicineNovocrania anomalaVillosa lienosaDaphnia pulexSagitta sp.Pectinaria gouldiiSymbion americanusNuculana pernulaSepia esculentaEnucula tenuisSolemya velumLineus lacteusTubulanus polymorphus-StruckGnathostomula paradoxaBoccardia proboscideaMacellomenia schanderiLaevipilina hyalinaTubulanus polymorphus-HalanychBryozoaPomatoceros lamarckiiSepioteuthis lessonianaParanemertes peregrinaMalacobdella grossaHemithiris psittaceaLeptochiton rugatusTrochozoaBrachionus plicatilisSpathoderma clenchiLaqueus californicusPatella vulgataLottia giganteaCrepidula fornicataPhoronidaAplysia californicaGlottidia pyramidataPhoronis psammophilaSchmidtea mediterraneaAlexandromenia crassaBrachiopodaMegadasys sp.Octopus vulgarisCapitella teletaNeomenia carinatacompositional heterogeneityNemerteaPhenacolepas pulchellaGadila tolmieiMolluscaMacrodasys sp.Crassostrea gigasPedicellina cernuaTaenia pisiformisDosidicus gigasCephalothrix linearisSpiralia
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