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Data from: Microbial consortia controlling biogenic gas formation in the Qaidam Basin of western China
负责人:
关键词:
Gas well;Microbial consortia;Salinity
DOI:
doi:10.5061/dryad.4h6v0
摘要:
mL?1 of water, and those of archaea ranged from 2.44?×?103 to 4.66?×?107 copies mL?1 of water. Both bacterial and archaea 16?s rRNA gene copies were negatively
Data from: Taxon abundance, diversity, co-occurrence and network analysis of the ruminal microbiota in response to dietary changes in dairy cows
负责人:
Tapio, Ilma
关键词:
Diet Bacteria Protozoans Fungi Archaean biology Archaeal taxonomy Oils
DOI:
doi:10.5061/dryad.t6t0q
摘要:
. QPCR analysis showed that the total amounts of bacteria, archaea or ciliate protozoa were not significantly altered either by FC ratio or addition
Data from: Phylogenetic ecology of widespread uncultured clades of the Kingdom Euryarchaeota
负责人:
Barberan, Albert
关键词:
Community Ecology Macroevolution Microbial Biology Molecular Evolution Phylogeography Speciation
DOI:
doi:10.5061/dryad.8490
摘要:
ecology approach in the Kingdom Euryarchaeota (Archaea) to gain insight into the environmental distribution and evolutionary history of one of the mos
Data from: A jungle in there: bacteria in belly buttons are highly diverse, but predictable
负责人:
关键词:
navel;biodiversity;bacteria;Belly button;core microbiome;oligarch;rain forest
DOI:
doi:10.5061/dryad.q8f74
摘要:
on >80% humans. While these frequent bacterial phylotypes (the archaea were all rare) are a tiny part of the total diversity of bacteria in human navels
Data from: Phylogenetically driven sequencing of extremely halophilic archaea reveals strategies for static and dynamic osmo-response
负责人:
关键词:
DOI:
doi:10.5061/dryad.1546n
摘要:
biological systems. To improve understanding of osmoadaptive strategies, we have generated 59 high-quality draft genomes for the haloarchaea (a euryarchaeal clade
Data from: The effects of model choice and mitigating bias on the ribosomal tree of life
负责人:
关键词:
Trichoplax adhaerens;Cyanophora paradoxa;Desulfurispirillum indicum;Chlamydomonas reinhardtii;Bigelowiella natans;Cenarchaeum symbiosum;Cryptosporidium muris;Zymomonas mobilis;Nitrosoarchaeum limnia;Lactobacillus fermentum;Aspergillus flavus;Oscillibacter valericigenes;Arachnula sp;Archaeoglobus fulgidus;single-matrix model;Thermoplasma acidophilum;Paenibacillus sp;Perkinsus marinus;Corynebacterium pseudotuberculosis;Natromonas pharaonis;Staphylothermus marinus;two-domain tree;Diplonema sp;Prevotella denticola;Cyanothece sp;Ribosomal tree of life;Candida albicans;Anaerolinea thermophila;Methanocaldococcus jannaschii;Phaeodactylum tricornutum;Methylacidiphilum infernorum;Methanosarcina mazei;Dictyostelium discoideum;Chlorobium limicola;Thermotoga maritima;Methanosphaera stadtmanae;Babesia bovis;Thermodesulfatator indicus;Thermovibrio ammonificans;Flamella sp;Korarchaeum cryptofilum;Syntrophus aciditrophicus;Methanobrevibacter smithii;Deinococcus deserti;Gemmatimonas aurantiaca;Dyadobacter fermentans;Methanococcus aeolicus;Tribonema sp;Toxoplasma gondii;Acetobacter pasteurianus;Methanococcoides burtonii;Leishmania major;Thalassiosira pseudonana;Aeropyrum pernix;Nitrosomonas europaea;mixture model;Thermococcus kodakarensis;Arabidopsis thaliana;Apis mellifera;Nitrosopumilis sp;Halobacterium salinarum;Acidilobus saccharovorans;Pyrobaculum aerophilium;Fibrobacter succinogenes;Acanthamoeba sp;Idiomarina loihiensis;Ciona intestinalis;Meiothermus silvanus;Thermocrinis albus;Neisseria meningitidis;Spirochaeta coccoides;Methanopyrus kandleri;Xylella fastidiosa;Bodo sp;Ignicoccus hospitalis;Physarum polycephalum;Desulfurococcus mucosus;Danio rerio;Compositional heterogeneity;Treponema brennaborense;Sulfolobus solfataricus;Hypterthermus butylicus;Picrophilus torridus;Plasmodium vivax;Denitrovibrio acetiphilus;Haloarcula marismortui;three-domain tree;Metallosphaera sedula;Phytophthora infestans;Planctomyces brasiliensis;Thermovirga lienii;Trypanosoma brucei;Dictyoglomus thermophilum;Cryptobacterium curtum;Trimastix pyriformis;Cryptococcus gattii;Dehalococcoides ethenogenes;Pyrolobus fumarii;Guillardia theta;Methanoculleus marisingri;Thermus scotoductus;Syntrophothermus lipocalidus;Coraliomargarita akajimensis;Desulfobacca acetoxidans;Nitrosospira multiformis;Heterosigma sp;Prochlorococcus marinus;Fusobacterium nucleatum;Rhodopirellula baltica;Emiliana huxleyi;Nanoarchaeum equitans;Pyrococcus horikoshii;Ostreococcus tauri;Euglena sp
DOI:
doi:10.5061/dryad.7785h
摘要:
Deep-level relationships within Bacteria, Archaea, and Eukarya as well as the relationships of these three domains to each other require resolution
Data from: Vascular plants mediate the effects of aridity and soil properties on ammonia-oxidizing bacteria and archaea
负责人:
关键词:
bacteria;Organic C;pH;ammonium;amoA genes;Drylands;aridity;Stipa tenacissima;Holocene;Archaea
DOI:
doi:10.5061/dryad.m827p
摘要:
An integrated perspective of the most important factors driving the abundance of ammonia-oxidizing bacteria (AOB) and archaea (AOA
Data from: Horizontal gene transfer of acetyltransferases, invertases and chorismate mutases from different bacteria to diverse recipients
负责人:
Baum, Thomas
关键词:
plant-parasitic nematodes horizontal gene transfer phylogenetics model selection analysis evolution
DOI:
doi:10.5061/dryad.pb68n
摘要:
of bacterial GNATs, INVs and CMs with diverse eukaryotes and archaea. There were at least eleven and eight well-supported clusters of GNATs and INVs, respective
Data from: Contrasting taxonomic stratification of microbial communities in two hypersaline meromictic lakes
负责人:
关键词:
Archaea;hypersaline meromictic lakes;bacteria;biogeochemical cycling;methanogenesis;prokaryotic diversity;ultrasmall uncultivated Archaea;deep coverage SSU rDNA amplicon sequencing
DOI:
doi:10.5061/dryad.2gm06
摘要:
sed cell density and was populated mostly by Archaea within oxic strata. In spite of their contrasting diversity, the microbial populations indigenous to each lake

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