Total counts of marine bacteria include a large fraction of non-nucleoid-containing bacteria (ghosts).
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Phylogeny of culturable estuarine bacteria catabolizing riverine organic matter in the northern Baltic SeaCulturability and coexistence of colony-forming and single-cell marine bacterioplanktonDetermination of Active Marine Bacterioplankton: a Comparison of Universal 16S rRNA Probes, Autoradiography, and Nucleoid StainingSuccession and diel transcriptional response of the glycolate-utilizing component of the bacterial community during a spring phytoplankton bloomSignificance of viral lysis and flagellate grazing as factors controlling bacterioplankton production in a eutrophic lake.Effectiveness of SYTOX Green stain for bacterial viability assessment.Rapid determination of bacterial abundance, biovolume, morphology, and growth by neural network-based image analysisAre uncultivated bacteria really uncultivable?Utility of green fluorescent nucleic acid dyes and aluminum oxide membrane filters for rapid epifluorescence enumeration of soil and sediment bacteriaImmunochemical detection and isolation of DNA from metabolically active bacteria.Combined microautoradiography-16S rRNA probe technique for determination of radioisotope uptake by specific microbial cell types in situVisualization and enumeration of marine planktonic archaea and bacteria by using polyribonucleotide probes and fluorescent in situ hybridizationDoes the high nucleic acid content of individual bacterial cells allow us to discriminate between active cells and inactive cells in aquatic systems?Abundances, identity, and growth state of actinobacteria in mountain lakes of different UV transparency.Relationship between the Intracellular Integrity and the Morphology of the Capsular Envelope in Attached and Free-Living Marine Bacteria.Increase in Fluorescence Intensity of 16S rRNA In Situ Hybridization in Natural Samples Treated with Chloramphenicol.Ecological implications of an improved direct viable count method for aquatic bacteriaA novel staining protocol for multiparameter assessment of cell heterogeneity in Phormidium populations (cyanobacteria) employing fluorescent dyesDiversity of Microbial Communities in Production and Injection Waters of Algerian Oilfields Revealed by 16S rRNA Gene Amplicon 454 Pyrosequencing.Influence of water chlorination on the counting of bacteria with DAPI (4',6-diamidino-2-phenylindole).Dominant marine bacterioplankton species found among colony-forming bacteria.What difference does it make if viruses are strain-, rather than species-specific?Single-cell enumeration of an uncultivated TM7 subgroup in the human subgingival crevice.Factors controlling bacteria and protists in selected Mazurian eutrophic lakes (North-Eastern Poland) during spring.Prokaryotic community analysis with CARD-FISH in comparison with FISH in ultra-oligotrophic ground- and drinking water.Widespread N-acetyl-D-glucosamine uptake among pelagic marine bacteria and its ecological implications.Significance of size and nucleic acid content heterogeneity as measured by flow cytometry in natural planktonic bacteria.Application of neural computing methods for interpreting phospholipid fatty acid profiles of natural microbial communities.Resolution of viable and membrane-compromised bacteria in freshwater and marine waters based on analytical flow cytometry and nucleic acid double staining.Spatial heterogeneity of bacterial populations along an environmental gradient at a shallow submarine hydrothermal vent near Milos Island (Greece).Large fraction of dead and inactive bacteria in coastal marine sediments: comparison of protocols for determination and ecological significanceUse of green fluorescent protein to monitor survival of genetically engineered bacteria in aquatic environments.Viral production, decay rates, and life strategies along a trophic gradient in the North Adriatic Sea.In situ analysis of nucleic acids in cold-induced nonculturable Vibrio vulnificus.Use of nucleic acid dyes SYTO-13, TOTO-1, and YOYO-1 in the study of Escherichia coli and marine prokaryotic populations by flow cytometryCytometric patterns reveal growth states of Shewanella putrefaciens.Geographic and phylogenetic variation in bacterial biovolume as revealed by protein and nucleic acid stainingRespective roles of culturable and viable-but-nonculturable cells in the heterogeneity of Salmonella enterica serovar typhimurium invasiveness.Contribution of Archaea to total prokaryotic production in the deep Atlantic Ocean.Prediction of effective genome size in metagenomic samples.
P2860
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P2860
Total counts of marine bacteria include a large fraction of non-nucleoid-containing bacteria (ghosts).
description
1995 nî lūn-bûn
@nan
1995 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
1995 թվականի հունիսին հրատարակված գիտական հոդված
@hy
1995年の論文
@ja
1995年学术文章
@wuu
1995年学术文章
@zh-cn
1995年学术文章
@zh-hans
1995年学术文章
@zh-my
1995年学术文章
@zh-sg
1995年學術文章
@yue
name
Total counts of marine bacteri ...... -containing bacteria (ghosts).
@ast
Total counts of marine bacteri ...... -containing bacteria (ghosts).
@en
Total counts of marine bacteri ...... n-nucleoid-containing bacteria
@nl
type
label
Total counts of marine bacteri ...... -containing bacteria (ghosts).
@ast
Total counts of marine bacteri ...... -containing bacteria (ghosts).
@en
Total counts of marine bacteri ...... n-nucleoid-containing bacteria
@nl
prefLabel
Total counts of marine bacteri ...... -containing bacteria (ghosts).
@ast
Total counts of marine bacteri ...... -containing bacteria (ghosts).
@en
Total counts of marine bacteri ...... n-nucleoid-containing bacteria
@nl
P2860
P1476
Total counts of marine bacteri ...... -containing bacteria (ghosts).
@en
P2093
Hagstrom A
Zweifel UL
P2860
P304
P407
P577
1995-06-01T00:00:00Z