ライフサイエンスコーパス: taxa

1 terial communities, with signature bacterial taxa.

2 d local peaks of bloom-forming heterocystous taxa.

3 ssifications and objective comparisons among taxa.

4 h degree of worker polymorphism seen in many taxa.

5 ty (n = 41) mCTs with abundance of anaerobic taxa.

6 position had strong effects on most symbiont taxa.

7 iated with climate change across 35 plankton taxa.

8 traits across 19 wild and cultivated tomato taxa.

9 ontributed to their movement between several taxa.

10 expanded aggregates composed of one or a few taxa.

11 upon the removal of the most immune-dominant taxa.

12 t the magnitude of change often varies among taxa.

13 ring insect development are limited to a few taxa.

14 e driven by both disease-specific and shared taxa.

15 s for multiple diversity facets and for both taxa.

16 reveal a huge chemical diversity in the two taxa.

17 able among taxa and among populations within taxa.

18 has been observed in terrestrial and aquatic taxa.

19 ts or pie graphs that use color to represent taxa.

20 tems based on 624 published studies from 492 taxa.

21 ith any of the currently recognized teosinte taxa.

22 characterization of diverse feline pathogen taxa.

23 diversity or relative abundance of specific taxa.

24 e and information transmission in a range of taxa.

25 ever, FMT increased diversity and beneficial taxa.

26 variation in recombination is similar among taxa.

27 ed young has been reported in several animal taxa.

28 elop, and social chemosignals occur in avian taxa.

29 el VT, and number of exclusive and indicator taxa.

30 to infect several aquatic and hematophagous taxa.

31 ated maize and samples of reference teosinte taxa.

32 stomes and can accommodate a large number of taxa.

33 ed pine DNA and were free of exogenous plant taxa.

34 to the distance from genes in all great ape taxa.

35 d arthropod abundance, particularly for rare taxa.

36 interspecific variation compared with other taxa.

37 gevity and metabolic health conserved across taxa.

38 counting for phylogenetic relatedness of the taxa.

39 ition and size fraction segregated bacterial taxa.

40 d a dose-response concordance across KEs and taxa.

41 hnically feasible in a variety of plantation taxa.

42 pronounced, and also involved several fungal taxa.

43 ong negative relationships across nearly all taxa.

44 onal capacity can be traced back to specific taxa.

45 rts, as they have been lost twice in derived taxa.

46 r target interception across a wide range of taxa.

47 , was mitigated by the rapid spread of plant taxa.

48 d reconstruct the evolutionary past of these taxa.

49 und common responses to DMS across reef fish taxa - a preference for water with DMS and change in swi

50 dominantly assemble by selective survival of taxa able to persist under extreme energy limitation.

51 he Human Microbiome Project which associates taxa abundances with KEGG orthology pathways.

52 station with WCR affected specific microbial taxa (Acinetobacter, Smaragdicoccus, Aeromicrobium, Acti

53 lications for diverse life-history traits in taxa across entire lake food webs.

54 us probe 2 were the most frequently detected taxa across the plaque groups, followed by Streptococcus

55 an effective means of reducing the number of taxa affected, averting the ecological impacts of night-

56 the most sulfidic samples were dominated by taxa affiliated with CH4 oxidizing, fermenting and SO42-

57 Additionally, the short recovery of many taxa after the bloom indicates that bacterial communitie

58 jor extant primate groups and three outgroup taxa, after an extensive literature survey and dissectio

59 structure were driven by the arrival of new taxa and a higher proportion of large, warm-adapted spec

60 alence of particle-associated SO42--reducing taxa and abundant sulfur-oxidizing taxa in both size fra

61 to climate drivers was highly variable among taxa and among populations within taxa.

62 e swings on genetic diversity across diverse taxa and between continents.

63 tion is likely to further exacerbate loss of taxa and ecosystem alteration, especially in drying clim

64 ith species richness in a wide range of wild taxa and ecosystems.

65 ps in the ocean's interior, but the relevant taxa and energy sources remain enigmatic.

66 using MOTHUR and vegan to identify bacterial taxa and evaluate changes in rhizosphere bacterial commu

67 hypothesis that beech trees select specific taxa and functions in their rhizosphere based on the soi

68 We also identify the taxa and geographic regions with the largest estimated n

69 However, observed shifts across taxa and geographical locations are highly variable and

70 ed on the biological response of terrestrial taxa and habitats to urbanization.

71 nstrain low latitude range edges across many taxa and habitats.

72 a genetic basis to delineation the candidate taxa and insight into the levels of genetic cohesion ass

73 t is highly conserved in many non-vertebrate taxa and may protect cells against hypoxia and oxidative

74 In addition, biases among taxa and organization levels provide a truncated picture

75 inal birth associated taxa, ii) skin derived taxa and other typical early colonisers such as Streptoc

76 alized sensory organs, match those of modern taxa and suggest that they had a mushroom feeding biolog

77 lyses include both broad taxon sampling (119 taxa) and 18 fossil calibrations across all Cyanobacteri

78 ronically rare species are distributed among taxa, and among the world's ecosystems and regions.

79 rain levels, quantify relative abundances of taxa, and classify individual reads to the species level

80 vealing the vulnerability of large and small taxa, and identifying size-specific threats.

81 sment of the evolution of GRNs between these taxa, and no study has attempted to determine the interp

82 n of conservation 'rules of thumb' for these taxa, and supports the notion of local focus as the most

83 r structuring soil communities than abundant taxa, and that these rarer taxa are better predictors of

84 y differential relative abundances of shared taxa, and unique microbiomes in kogiid hosts compared to

85 the divergence times of sister intraspecific taxa, and when they do little is said about this subject

86 Its presence in the major eukaryotic taxa-animals, plants, and protists (including important

87 However, specific microbial taxa are associated with colonization of this important

88 ies than abundant taxa, and that these rarer taxa are better predictors of community structure than e

89 IMS data for the two highest delta(13)C Apex taxa are consistent with those of extant phototrophic ba

90 cific taxon ages indicates that indeed these taxa are expected to be < 10 million yr old.

91 t genetic background, potentially cariogenic taxa are likely not controlled by genetic factors.

92 y, the delta(13)C values of each of the five taxa are lower than those of bulk samples of Apex keroge

93 We find that rarer taxa are more important for structuring soil communities

94 d there is a poor understanding for why some taxa are more sensitive to climate than others.

95 The new volant taxa are phylogenetically nested with arboreal eleuthero

96 -20% loss in cooler, wetter ecoregions where taxa are relatively buffered from projected warming and

97 Closely related taxa are, on average, more similar in terms of their phy

98 complexes: It has been used to identify some taxa as belonging to the same biological species as well

99 phylogeny of 979 taxa (including 23 outgroup taxa, as well as 61 orders, 175 families and 496 genera)

100 l analysis shows significant increases in 12 taxa associated with gum health including Neisseria spp.

101 High-throughput sequencing identified 43 taxa associated with HS lesions.

102 culum, Bifidobacterium and Coriobacteriaceae taxa associated with lean phenotype, increased in WD + P

103 sseria spp. and a significant decrease in 10 taxa associated with periodontal disease including Trepo

104 ts nirS sequences, and to identify indicator taxa associated with those environmental characteristics

105 terized by a greater frequency of pathogenic taxa at high relative abundance and reduced Streptococcu

106 comprise only a slightly smaller fraction of taxa at higher vs. lower latitudes (8% vs. 11% of genera

107 bial activity against a variety of bacterial taxa at low micromolar concentrations.

108 ed on the basis of their ability to identify taxa at the genus, species, and strain levels, quantify

109 relative abundances of several gut bacteria taxa, Bacteroides and Prevotella in particular, differed

110 e resilience to warming until refuge-forming taxa become imperiled.

111 asmobranch fishes are among a broad range of taxa believed to gain positional information and navigat

112 tion to resistance evolution across multiple taxa but are clinically mild and thus present easier tar

113 As were not specific to individual bacterial taxa but rather polyreactive, with broad reactivity to a

114 exual behaviour occurs across diverse animal taxa, but adaptive explanations can be difficult to dete

115 A given set of taxa can be related in a limited number of ways, but if

116 ingly clear that gene flow between divergent taxa can generate new phenotypic diversity, allow for ad

117 microscopic data, we propose three candidate taxa: 'Candidatus Syngnamydia medusae', 'Candidatus Medu

118 Strikingly, taxa carrying the complete ortholog of PRDM9 are precise

119 Across the 147 biota samples (18 taxa) collected, perfluorooctane sulfonate (PFOS), perfl

120 s revealed that the soil type determines the taxa colonizing the beech rhizosphere.

121 HCT recipients, with loss and appearance of taxa common on short time scales.

122 the genera Akkermansia and Lachnospiraceae, taxa commonly associated with metabolic health.

123 erved the enrichment of bacterial and fungal taxa commonly found in drinking water distribution syste

124 ow-P soils and identified a set of 15 fungal taxa consistently detected in its roots.

125 n on photosynthetic traits within and across taxa dampens the effects of temperature on GPP across a

126 running time for this computation on the 349 taxa dataset by 99%.

127 Seven of the taxa declined at rates of up to 8% per year.

128 espite being vertically separated, indicator taxa deposited under OMZ conditions were more similar to

129 acteroidetes, and Actinobacteria as the main taxa despite the cyanobacterial species present and geog

130 Cytosponge samples contained the majority of taxa detected in biopsy and brush samples, but were enri

131 analysed genomic data from approximately 500 taxa detected in this study, for which data were availab

132 Unlike their European counterparts, ENA taxa do not share common southern centres of haplotype e

133 R analysis confirmed that distinct bacterial taxa dominate in different placental niches.

134 Rhizobial taxa dominate N-fixing tree richness at lower latitudes,

135 Furthermore, the set of taxa driving functional shifts and their contribution le

136 ors, and proportions of individual microbial taxa during OH abstention.

137 rans) relative to small-bodied, cold-adapted taxa (e.g., chironomids and oligochaetes).

138 ting results from 51 studies across multiple taxa encompassing over 11,000 species' responses for 54

139 n empirical designation of rare and abundant taxa enlightens us on the structure of endophyte communi

140 5 million yr old or younger, with only 4% of taxa estimated to be over 10 million yr old or older.

141 oes not show any sign of saturation and most taxa even show increases in the rate of first records ov

142 only observed for plants and animals whereby taxa exhibit decreased latitudinal range sizes closer to

143 ng niche plasticity and 99 km per decade for taxa exhibiting niche conservatism.

144 ement between 7 km per decade northwards for taxa exhibiting niche plasticity and 99 km per decade fo

145 soil bacterial and archaeal taxa, with these taxa exhibiting similar temperature responses across a b

146 y systems has been documented across distant taxa, fewer studies have investigated how changes in beh

147 ses (e.g., abundance and richness of nursery taxa, flow attenuation).

148 species pools (sets of potentially suitable taxa) for each site, which are expected to reflect regio

149 asing precipitation, but also differed among taxa, for instance Oribatida responded negatively to her

150 how that over 90% of the intraspecific plant taxa found in a literature search are estimated to be 5

151 ey information that unites several enigmatic taxa from across Pangaea into a previously unrecognized

152 processes occur in a wide variety of animal taxa, from insects to cetaceans.

153 Two main additional taxa, Fusobacterium and Parvimonas, correlated with the

154 The problematic fossil taxa Halkieria and Orthrozanclus (grouped in Sachitida)

155 Empirical studies on a diverse array of taxa have demonstrated support for the CMH.

156 Several taxa have socioeconomic significance, being important or

157 lly larger labyrinths than actively swimming taxa (i.e., all other sauropterygians).

158 found in the seed oils of two endemic Borago taxa, i.e. B. morisiana (24.4 and 24.6% GLA of total fat

159 Given the low number of taxa identified when coupling shotgun data with clade-ba

160 A scan for diversifying selection across taxa identifies strong and highly polygenic selection si

161 of i) intrauterine/vaginal birth associated taxa, ii) skin derived taxa and other typical early colo

162 tected 31 pathogens comprising nine pathogen taxa in 28 felid samples analyzed.

163 s of clades only when inconsistent with most taxa in a phylogenetic tree.

164 species are one of the key structure-forming taxa in benthic communities on the Antarctic continental

165 d phenomenon, observed across a multitude of taxa in both laboratory and natural conditions.

166 -reducing taxa and abundant sulfur-oxidizing taxa in both size fractions across the oxic-anoxic inter

167 ic data sets (chloroplast DNA) from 14 woody taxa in Eastern North America (ENA) to data sets from 21

168 richness and abundances of various bacterial taxa in gut microbiota.

169 The abundance of a number of bacterial taxa in house dust was associated with increased or decr

170 s, we identified DP-associated gut bacterial taxa in individuals either practicing chronic calorie re

171 tivores constitute two co-dominant predatory taxa in many ecosystems, and the emergent properties of

172 led the distribution of 88 individual insect taxa in relation to existing combinations of maximum sum

173 al model for habitat partitioning among mice taxa in settlements of varying durations.

174 ancestor of the extant reptiles and various taxa in Squamata, one of the main competitors of the tem

175 e abundance of sequence reads from bacterial taxa in stool samples over time.

176 less complex correlations between bacterial taxa in the protist-grazed treatments with a higher prop

177 g limited intraguild predation between these taxa in this system.

178 change projections indicate a 30-40% loss of taxa in warmer, drier ecoregions and 10-20% loss in cool

179 lyses considered 16 dominant mesozooplankton taxa (in terms of biomass and abundance) in the southwes

180 The most abundant taxa, in wild and laboratory populations, were Wiggleswo

181 orm, T-BAS v1.0 uses a core phylogeny of 979 taxa (including 23 outgroup taxa, as well as 61 orders,

182 erium, and Gemella) as well as several novel taxa (including increased frequencies of bacterial vagin

183 Several taxa, including Propionibacterium, showed a significantl

184 Exposures to several outdoor fungal spore taxa, including some not reported in previous research,

185 ected: a primary response in which surviving taxa increased in abundance; a secondary response phase

186 Analysis of specific fungal taxa indicated tree diversity effects at the local neigh

187 age, 21-fold more speciose than their sister taxa, indicating that a shift in diet is associated with

188 hod can infer the network topology and inter-taxa interaction types without assuming any particular p

189 analysis identified new potential bacterial taxa involved in amino acid degradation.

190 is result for the young age of intraspecific taxa is consistent with the earlier observation that pos

191 community of several trophically interacting taxa is frozen in time by exceptional preservation.

192 The importance of bioluminescent marine taxa is highlighted in the water column, as we showed th

193 and that runaway introgression between these taxa is unlikely.

194 teria in the oxycline's PA fraction included taxa known to be aerobic and anaerobic chemoorganotrophs

195 The sedDNA record contains 73 taxa (mainly genus or species), all but one of which are

196 ow that, when using strict criteria, extinct taxa marked by deep divergence times and a lack of close

197 tree species, suggesting that many tropical taxa may be physiologically incapable of tolerating dry

198 Because it occurs across diverse taxa, measurements of bioluminescence can be powerful to

199 nation systems during the evolution of these taxa, most frequently from female to male heterogamety.

200 e differential sensitivity of cyanobacterial taxa: nitrogen-fixing Scytonema spp. were the most sensi

201 In other taxa, NMP is primarily detoxified via a cytochrome P450

202 matched those of the principal biodegrading taxa observed in the field, including the DWH Oceanospir

203 d ventral mesothoracic chaetae, confirmed 18 taxa of 22 molecular units, with six of them described a

204 sequencing, we identified the main bacterial taxa of burnt holm-oak rhizosphere, then we obtained an

205 These rare taxa of normal skinfold microbiota were associated with

206 spectroscopy (SIMS) of 11 specimens of five taxa of prokaryotic filamentous kerogenous cellular micr

207 ce genomic information is gathered for other taxa of the family Rivulidae that do not self-fertilize.

208 climate variability, we analyzed 73 diverse taxa off the southeast US coast in 26 years of scientifi

209 ividual level, network analysis of microbial taxa on infected fish revealed the association of multip

210 hat positive effects of particular microbial taxa on multifunctionality resistance could potentially

211 s, we have emphasized the impact of specific taxa or communities thereof.

212 At least for certain taxa, our analysis provides evidence of their paleoenvir

213 tance of branching morphogenesis in multiple taxa, our findings have general importance outside mamma

214 riaceae, and iv) the appearance of adultlike taxa, particularly species associated with Blautia, Egge

215 and associated body mass of 69 notoungulate taxa, placed in their phylogenetic and geological contex

216 Across multiple taxa, population structure and dynamics depend on effect

217 Importantly, particular bacterial taxa predict the coral host response in a short-term hea

218 rs revealed a large core of shared microbial taxa, predominantly composed of microorganisms previousl

219 We identified a broad distribution of fungal taxa predominated by Chytridiomycota and Dikarya.

220 idian replicates) were identified, including taxa previously described in marine invertebrate microbi

221 Two gram-negative anaerobic rod taxa, Prevotella and Porphyromonas, predominated, contra

222 le they have been documented in a variety of taxa, primarily birds, they are rare outside non-human m

223 Taxa putatively associated with chemoautotrophic sulfur

224 amics and Bayesian networks implied that the taxa putatively not capable of extracellular electron tr

225 ed Streptococcus, Gemella, and Porphyromonas taxa relative abundance in patients with neutrophilic as

226 with distinct spatial distributions of some taxa relative to one another, notably at the border betw

227 tions largely excluded two equally important taxa, Remipedia and Cephalocarida.

228 he 18S rRNA sequences, we showed that fungal taxa represented between 0.93% and 60.32% of the eukaryo

229 e of specific eury- and mainly thaumarchaeal taxa, represented by a core archaeome of the human skin.

230 Sixty-seven taxa representing all evacanthine tribes and all regiona

231 broad diversity of eukaryotic and bacterial taxa reside on rock surfaces where they can influence th

232 ay be ecologically disruptive if interacting taxa respond oppositely to warming.

233 analysis applied to the top 25 most abundant taxa revealed 4 underlying bacterial coabundance groups;

234 opland led to greater catchment-level insect taxa richness (2.6-fold), pollinator abundance (3.5-fold

235 s these dietary induced alternations in this taxa's abundance.

236 Our analyses leverage the taxa-sample duality in the data to show how the gut micr

237 oportion of sequences from sewage-associated taxa (SAT) or pathogen-like sequences (PLS) were predict

238 n three endemic and vulnerable Mediterranean taxa: Scopoli's shearwater, Mediterranean shag, and Audo

239 archers who work with ovary RNA-seq in these taxa should realize that insufficient depletion of rRNA

240 ny of the organisms represent entirely novel taxa, showing that microbial diversity within the human

241 We identified 40 taxa significantly associated with inflammation, includi

242 mination systems are highly variable in many taxa, sometimes even between closely related species.

243 eater focus should be placed on less-studied taxa such as many families of Coleoptera, Diptera, and H

244 standing the susceptibility of highly mobile taxa such as migratory birds to global change requires i

245 northern hemisphere have found that dominant taxa, such as calanoid copepods, have conserved their th

246 onin-containing neurons in major tetraconate taxa suggest a close phylogenetic relationship of Remipe

247 ugh time, but consistent presence of similar taxa suggested dispersal and/or common selective pressur

248 on of gene regulatory networks across higher taxa supports generalizations made from a limited number

249 bacteria, specifically a few highly abundant taxa (Synechococcus and Cyanobium) with a long tail of l

250 by the quantitative frequencies of these key taxa than by classifying communities into five community

251 dies comparing only a few, distantly related taxa that differ in many aspects of their biology beside

252 oach to study predator-prey relationships in taxa that do not lend themselves to morphological identi

253 of H. heliophila represent nitrogen cycling taxa that have the potential to contribute to a diverse

254 y broad diets, and the increased richness of taxa that include plants in their diet likely results fr

255 cal American diet reflects a durable loss of taxa that is replenished only when dietary manipulation

256 utilize host-derived substrates and disfavor taxa that prefer complex plant polysaccharides.

257 ved changes in community composition towards taxa that produce relatively more siderophores following

258 we assess population trends of ten shorebird taxa that refuel on Yellow Sea tidal mudflats, a threate

259 ly Jurassic by forests dominated by high-LMA taxa that were likely to have slower metabolic rates.

260 sequencing identified 202 and 171 bacterial taxa that were significantly (false discovery rate < 0.0

261 were found, we identified specific bacterial taxa that were significantly associated with MS.

262 largely driven by community changes in rare taxa, those taxonomic units that made up less than 0.31%

263 The differing responses of taxa to global warming will cause spatial restructuring

264 ta-analysis of the pH sensitivities of local taxa, to investigate the direct and indirect effects of

265 In total, 147 AMF virtual taxa (VT) were detected, including 22 VT new to science.

266 obiota, the presence of 3 distinct bacterial taxa was correlated with protection against CDI: Bactero

267 For example a study of 349 primate taxa was estimated to require over 9 months of processin

268 Previous recognition of these taxa was hampered by the lack of a distinguishing phenot

269 uadorian babies involved different bacterial taxa, was more pronounced, and also involved several fun

270 Surprisingly, humans are one of the few taxa we studied in which the thumb musculoskeletal struc

271 acting with taxonomically distinctive native taxa, we found that consumption and growth were particul

272 ons between diploid and (usually) tetraploid taxa, we know very little about how elevated ploidy abov

273 among studies and complex interactions among taxa, we merge 30 independent bacterial data sets compri

274 es and transcriptomes across 37 deuterostome taxa, we shed light on the evolution and diversity of TL

275 al diversity measures or abundances of major taxa, we show that disparate amplicon sequence data can

276 Core symbiont taxa were affiliated with phylogenetic lineages capable

277 ipal coordinates analysis, and 18 individual taxa were found to be significantly associated with GBS

278 environmental factors, highly heritable oral taxa were identified.

279 ional faunas, and fourteen putative outgroup taxa were included.

280 ve of fixed carrying capacities and abundant taxa were largely shared across individuals.

281 er bacteria and indicated that only very few taxa were positively correlated with Microcystis.

282 Relative numbers of certain bacterial taxa were significantly different between the microbiota

283 The range sizes of bacterial taxa were strongly correlated with latitude, decreasing

284 ation for read abundance differences between taxa, which would affect amplicon based and PCR free met

285 d exon 10 in CvAOXA is more conserved across taxa, while the first exon 10 in CvAOXB contains novel m

286 ity dynamics, identify potential 'indicator' taxa with an important role in structuring communities,

287 pecific inflammatory mediators and microbial taxa with clinical inflammation.

288 tasetinae, the angiosperm lineage richest in taxa with ESD.

289 Late Triassic forests, dominated by low-LMA taxa with inferred high transpiration rates and short le

290 ny plant groups, and especially monophyletic taxa with multiple base chromosome numbers, can result f

291 Bacterial taxa with protective effects against development of CDI

292 ow these patterns should generalize to other taxa with public goods behaviors.

293 n hibernators shifts the microbiota to favor taxa with the capacity to degrade and utilize host-deriv

294 Taxa with the greatest reliance on the Yellow Sea as a s

295 aea; and those for the two lowest delta(13)C taxa, with methane-metabolizing gamma-proteobacteria.

296 f 189 ubiquitous soil bacterial and archaeal taxa, with these taxa exhibiting similar temperature res

297 lationship has only been explored for select taxa, with variable results.

298 f diverse DNA sequences representing unknown taxa within a robust phylogenetic context, and to permit

299 p corresponds to modernization: Notably, the taxa within the Hadza that are the most seasonally volat

300 revealed that diet affects the most abundant taxa within the microbiome and that a specific group of