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松花湖水体中不同空间分布的细菌群落结构分析 Title:AnalysisofMicrobialCommunityStructureinDifferentSpatialDistributionsofMatangLake Abstract: Understandingthestructureanddynamicsofmicrobialcommunitiesinaquaticecosystemsiscrucialforassessingtheirecologicalfunctions.ThisstudyaimstoanalyzethemicrobialcommunitystructureindifferentspatialdistributionswithinMatangLake,focusingonthediversityandcompositionofbacteria.Samplecollectionwasperformedatfivedifferentsitesrepresentingvariouszones(openwater,littoralzone,andsubmergedvegetation)inMatangLake.High-throughputsequencingofthe16SrRNAgenewasconductedtoinvestigatethebacterialdiversityandcommunitycomposition.TheresultsofthisstudyprovideinsightsintotheecologicalrolesofmicrobialcommunitieswithinMatangLakeandcontributetotheoverallunderstandingofaquaticecosystemdynamics. 1.Introduction: Aquaticecosystems,includinglakes,playavitalroleinmaintainingglobalbiodiversityandecologicalbalance.Adiverserangeofmicroorganisms,especiallybacteria,contributesignificantlytothecyclingofnutrients,organicmatterdecomposition,andoverallecosystemfunctioning.Understandingthemicrobialcommunitystructureanditsspatialdistributionindifferentzonesofalakeprovidesvaluableinformationforenvironmentalmanagementandconservationefforts. 2.Methods: 2.1StudySiteandSampleCollection: MatangLake,locatedin[insertlocation],wasselectedasthestudysite.Fivesamplingsites,representingopenwater,littoralzone,andsubmergedvegetation,werechosenbasedontheirdistinctecologicalcharacteristics.Waterandsedimentsampleswerecollectedfromeachsiteusingappropriatesamplingequipment. 2.2DNAExtractionand16SrRNAGeneAmplification: TotalDNAwasextractedfromthecollectedsamplesusingacommercialDNAextractionkit.TheextractedDNAwasusedasatemplateforPCRamplificationoftheV3-V4regionofthe16SrRNAgene.PCRconditionsandprimersequenceswereadoptedfrompreviousstudies. 2.3High-ThroughputSequencingandBioinformaticsAnalysis: ThePCRproductswerepurified,quantified,andsubjectedtoIlluminaMiSeqsequencing.Rawsequencingdatawerethenprocessedusingbioinfor