ライフサイエンスコーパス: taxa

1 light muscle relative to low-altitude sister taxa.

2 tterns of distribution among Southeast Asian taxa.

3 ation dynamics across a wide range of animal taxa.

4 wo signaling systems among distantly related taxa.

5 ects of both undescribed species and missing taxa.

6 ity of CHC compounds across different insect taxa.

7 breeding is a key life-history stage for all taxa.

8 n of a wide range of social behaviors across taxa.

9 activity increased in only newly established taxa.

10 itu hybridization for 10 different bacterial taxa.

11 covery unevenly distributed among guilds and taxa.

12 "Return" southward movement occurred in most taxa.

13 leviating resource competition among endemic taxa.

14 aling pathways across different evolutionary taxa.

15 plied to study other genetically intractable taxa.

16 s between the isotopic ecology of both these taxa.

17 irming contrasting bleaching responses among taxa.

18 of light on environmental photoheterotrophic taxa.

19 tions for present and past conditions across taxa.

20 bility of NLR-Annotator across diverse plant taxa.

21 supported the persistence of the additional taxa.

22 rms that introduced new co-associations with taxa.

23 e significance has been reported in numerous taxa.

24 ies were solely associated with apicomplexan taxa.

25 lic repositories, thereby representing novel taxa.

26 itous (terrestrial and aquatic environments) taxa.

27 al associations with at least seven frondose taxa.

28 or, which are poorly known in high-elevation taxa.

29 water ecosystems have only targeted specific taxa.

30 gesting opportunistic proliferation of these taxa.

31 a compared with rhizomatous and nongeophytic taxa.

32 ncestral polymorphism or introgression among taxa.

33 ng the world's most biodiverse but imperiled taxa.

34 ryotic diversity or environmentally relevant taxa.

35 amounts of sequences assigned to planktonic taxa.

36 tial detectors of temperature changes across taxa.

37 ase relative to rhizomatous and nongeophytic taxa.

38 ccurrence networks, and a shift in indicator taxa.

39 dynamics drive the evolution of constituent taxa.

40 reductions in body size across these diverse taxa.

41 are essential for proper development across taxa.

42 d designs to incorporate lessons from fossil taxa.

43 or older women with many heritable microbial taxa.

44 rcozoans, Gastrotricha, or unicellular algal taxa.

45 ch antimicrobial differed within and between taxa.

46 Random forest analyses identify 12 taxa, 11 in the phylum Firmicutes, eight of which are po

47 social learning [1], is found across various taxa [2-6].

48 raging 674 OTUs) dominated by a few symbiont taxa (25 OTUs accounted for 64% of total relative abunda

49 tion, along with that of other Maastrichtian taxa (Acheroraptor and Dakotaraptor), suggests dromaeosa

50 l containing clinical features and bacterial taxa achieved an area under the curve (AUC) of 0.87 whic

51 of codependency, between plant and AM fungal taxa across locations.

52 tic relatedness between native and nonnative taxa across thousands of nested locations ranging in siz

53 tified seven ethnic group-specific bacterial taxa after adjusting for dental plaque index, decayed mi

54 gments was used to detect a total of 29 fish taxa among the analyzed samples.

55 l changes, a decrease in connectedness among taxa, an increase in fragmentation of taxon co-occurrenc

56 ies' response, we use a unique dataset of 91 taxa and 178 phenological events observed across a netwo

57 ting in enrichment of potentially pathogenic taxa and antimicrobial resistance genes.

58 the high levels of biodiversity-across many taxa and biomes-that agricultural landscapes can support

59 Studying the distribution of microbial taxa and genes across plant habitats has revealed the im

60 ities, revealing putative interactions among taxa and identifying correlations between these communit

61 studies show how they are applicable across taxa and in particular physical environmental situations

62 ial ossification sequences in extant saurian taxa and in well-preserved embryos of the early branchin

63 mists and the users of taxonomy decide which taxa and names should be used by society whilst continui

64 d to identify associations between bacterial taxa and NGU, and to select bacteria for targeted quanti

65 tructure illuminates the roles of individual taxa and provides insight into their community ecology a

66 s are detected is simply infeasible for many taxa and settings because of the vast numbers of animals

67 as greater restoration of butyrate producing taxa and survival after surgery improved (29% vs 79% vs

68 a predictive understanding of the microbial taxa and their activities that control the fate of oil s

69 gned to be massively scalable to hundreds of taxa and thousands of samples, and can be efficiently pa

70 Compositional PCA identified characterizing taxa and weightings for calculation of gut microbiota PC

71 the mesocosm samples represented uncultured taxa and were present typically as members of the rare b

72 om females to their eggs differed among bird taxa and with maternal THg exposure.

73 tively high (20 spore species and 17 virtual taxa) and both spore abundance and community structure s

74 ral populations (approximately species-level taxa) and improves average viral detection rates over vi

75 considered to be confined to certain animal taxa, and absent from photosynthetic eukaryotes.

76 ional because of large numbers of detectable taxa, and because microbiota characteristics are describ

77 literature review of 109 papers studying 129 taxa, and find that all five criteria are assessed for o

78 h cohort gut bacterial diversity, structure, taxa, and function at 6 weeks (n = 166), 1 year (n = 158

79 cting most invertebrates and other neglected taxa, and it is unclear whether well-studied taxa, such

80 e nature of these relationships between such taxa, and to understand the role of warm-blooded animals

81 sure, germination, and survivorship of these taxa, and we used the estimates to determine likelihood

82 bal commercial and cultural importance, as a taxa, anguillid eels can act as indicator, umbrella and

83 In conclusion, intestinal viral taxa are altered in fecal samples from patients with AH

84 We demonstrate that penile taxa are associated with HSV-2 in female partners, and v

85 d with HSV-2 in female partners, and vaginal taxa are associated with HSV-2 in male partners.

86 cading effects of biodiversity loss on other taxa are largely unknown because baseline data are often

87 gh potentials, further suggesting that those taxa are responsible for the bioelectroactivity.

88 nditions and we observed that rare microbial taxa are sample site rather than region specific.

89 en spatial pattern, motion detectors in both taxa are tuned to speed, selective for one of four cardi

90 escent analyses recovered almost all nominal taxa as "species".

91 cs recovers sessile, infaunal and tubicolous taxa as an early diverging grade(5).

92 nce networks points to these three expanding taxa as potential mediators of gut microbiome dysbiosis.

93 n demonstrated reduced butyrate contributing taxa as potentially responsible for failed recovery.

94 tter adapted to high temperatures than other taxa, as demonstrated by their physiology and evolutiona

95 Several bacterial taxa associated with high plaque index or high DMFT were

96 cellular electron transfer and the microbial taxa associated with the observed electroactivity are fu

97 Several taxa at 1, 2, and 3 years were associated with SRS-2 per

98 ifferences in relative abundance of specific taxa at both phylum and genus levels between WNH and BNH

99 In limited investigation of marine taxa at larger spatiotemporal scales, macroecologists an

100 Two hundred and six taxa at the species level were identified in sputum, mos

101 veral SNP were significantly associated with taxa at the three time points.

102 e biomass of four common grassland arthropod taxa-Auchenorrhyncha, sucking herbivores, Acrididae, che

103 hile promoting the growth of some widespread taxa benefiting from the decline of phytoplankton blooms

104 host specificity and differentially abundant taxa between different amoeba hosts.

105 ication of differentially abundant microbial taxa between experimental conditions is a methodological

106 The number of observed taxa between MCT and healthy skin surfaces was detected,

107 beginning to incorporate work on more insect taxa beyond Drosophila.

108 ed with PIME machine-learning de-noising and taxa binning/parsing of prevalent ASVs at the single nuc

109 Neo-sex chromosomes are found in many taxa, but the forces driving their emergence and spread

110 absolute abundances of individual bacterial taxa by combining the precision of digital PCR with the

111 pigmentation increased significantly across taxa by ~2% per year.

112 ling pathway impacts lifespan across distant taxa, by controlling the activity of nodal transcription

113 ansplantation or defined commensal bacterial taxa can prevent or treat FA.

114 her communities (e.g. those working on other taxa) can adapt our successful model.

115 0) (PERMANOVA P < 0.001) based on microbiome taxa clustering and neurocircuit-relevant metabolic path

116 diversity of cichlid radiation because other taxa coexistent with the Cichlidae demonstrate lower spe

117 sification for bulbous, cormous and tuberous taxa compared with rhizomatous and nongeophytic taxa.

118 inical samples can be arduous, the number of taxa considered in any one study often exceeds the numbe

119 le-aged individuals, but also a novel set of taxa consistently gained in disease across all age group

120 Many taxa could become extinct in this century.

121 Some abundant eukaryotic cold water taxa could persist, while less abundant eukaryotic taxa

122 between the bloom dominant species and other taxa could play a role in the interplay of microbial com

123 ion/extrapolation approach to a global multi-taxa dataset from disturbed forests, including birds, pl

124 Fish comprised only 0.07% of the taxa detected by a broad COI primer, yet included 43 spe

125 Pairwise comparisons showed that 9 and 23 taxa differed between controls and CD patients with acti

126 ponse to [CO(2)] with significant [CO(2)] by taxa differences beginning at 122-124 days after sowing

127 The relevant taxa differentially encode specific functions that are k

128 Furthermore, within lineages, different taxa display evidence of increased relative abundance in

129 es), with Candida and Malassezia as the main taxa driving cluster partitioning.

130 at toxicity risk of MeHg can vary among bird taxa due to differences in maternal transfer of MeHg to

131 organelle genomes in a wide distribution of taxa encompassing plants and protozoans.

132 Among the taxa enriched by infection with the fast-spreading virus

133 ies, which are still unknown for hundreds of taxa, especially Asian ones.

134 Among the taxa examined, we find muscle-powered and fully fledged

135 All taxa exhibited frequent flights on southerly winds, acco

136 crania and low bite forces and ornithischian taxa exhibiting character complexes associated with exte

137 d and compared the distribution of eight oak taxa for the present and two paleoclimatic environments,

138 were inhabited by phylogenetic relatives of taxa for which laboratory growth is not known at >45 deg

139 e more highly enriched in moldy homes and 14 taxa from Ascomycota, Basidiomycota, and Zygomycota that

140 Several taxa from Cyanobacteria, Bacteroidetes, and Fusobacteria

141 We could also discriminate extant taxa from extinct species when adult birds were included

142 rature and biogeographical analyses of other taxa from South and Southeast Asia, contribute to an imp

143 Taxa from the Northern Hemisphere are disproportionately

144 reased C(4) grazing by cooccurring mammalian taxa from the same sequence.

145 ne halophilic and xerophilic fungi including taxa grouping into Ascomycota and Basidiomycota, capable

146 Seventy taxa had a substantial proportion (>30%) of habitat impa

147 A random forests classifier based on these taxa had an AUROC of 0.90 to predict advanced fibrosis.

148 gly, neither immigrants nor drought-tolerant taxa had higher abundance in dispersal treatments.

149 For two exemplar taxa, Haemophilus parainfluenzae and the genus Rothia, m

150 ntly, in immune-oncology, specific microbial taxa have been described to enhance the effects of thera

151 Historical declines in multiple insect taxa have been documented across the globe in relation t

152 ttempts to barcode various Solenopsidini ant taxa (Hymenoptera: Formicidae: Myrmicinae), including th

153 Concerningly, many of the bacterial taxa identified here as contaminants have been reported

154 More broadly, across taxa, imperfect coordination of collective behaviors mig

155 ently and across more distantly related host taxa in alpha- than beta-CoVs, and is more highly constr

156 ve abundance of diverse fungal and bacterial taxa in both 3-wk-old and 7-wk-old plants.

157 ite studies on more than two dozen mammalian taxa in captivity, evidence for male-mediated maturation

158 Moreover, the proportion of fungal taxa in common between the sputum and EDC samples was si

159 The representation of these 14 duodenal taxa in fecal microbiota was significantly different fro

160 e primary outcome was difference in specific taxa in fecal or intestinal tissue samples from patients

161 sed analyses were used to identify bacterial taxa in fecal samples at ages 6, 12, 18, and 24 months (

162 Analysis of the abundances of coral taxa in fossil bulk samples define the Historical Range

163 These interplays with discriminant bacterial taxa in HT and NT subjects highlight the potential role

164 l microbes, especially the most diverse rare taxa in maintaining community diversity and multifunctio

165 were enriched with Pseudomonas, the dominant taxa in MWF.

166 r dispersal rate but a larger pool of native taxa in North versus South America.

167 he day and night vertical distribution of 46 taxa in relation to environmental conditions.

168 ut resulted from higher extinction of native taxa in southern South America.

169 iments and underscore the role of uncultured taxa in such efforts.

170 siderophore-like BGCs can be identified from taxa in the adult gut microbiome that have rarely been r

171 ribosome organization that are exhibited by taxa in the human oral microbiome.

172 he dispersal and diversification patterns of taxa in this biodiverse and geologically complex region.

173 e bacterial diversity and specific bacterial taxa in wine, with potential consequences for wine quali

174 Other abundant taxa included Actinomyces (10.5%), Olsenella (9.4%), Pre

175 depletion and presence of specific anaerobic taxa including Megasphaera, Prevotella timonensis and Ga

176 Penile taxa (including Ureaplasma and Aerococcus) were associat

177 grounds have been observed across biological taxa, including birds, mammals, and insects.

178 Here we illustrate that key sulfur-cycling taxa, including Dethiobacter, Desulfitispora and 'Desulf

179 rence point for the social evolution of many taxa, including our own species.

180 ression may have also played a role in other taxa, including vagrant species R. arbuscula, R. haydeni

181 Various taxa increased, including Fusobacterium, Actinomyces, an

182 ovide a more direct test to assign candidate taxa into subspecies or species categories.

183 One of these taxa is a new cloudinid from Mongolia, Zuunia chimidtser

184 ngly underpinning that hybridization between taxa is commonplace, challenging our views on the mechan

185 is not a result of lumping together diverse taxa; it holds within all subgroups of organisms we exam

186 In higher taxa, kin recognition occurs via visual, chemical, or ta

187 BAs to SBAs, and Ruminococcaceae (one of few taxa known to include SBA-producing bacteria).

188 vated abundances of members of the bacterial taxa Lachnospiraceae and Enterococcaceae were associated

189 In the case of carnivorous taxa, Late Miocene pre-GABI endemic sparassodonts consum

190 egulatory networks for this trait in diverse taxa, leading to new knowledge about how and why develop

191 om those of wood-rotting and ectomycorrhizal taxa, likely reflecting contrasts in their fundamental b

192 elated with increased abundance of microbial taxa linked to BA metabolism.

193 predictable from linear combinations of the taxa maintained on each individual metabolite in the mix

194 We found that 7.1% of the taxa may be critically endangered in their natural habit

195 ssion process and functional changes of rare taxa may be important in elucidating the ecosystem stabi

196 ould persist, while less abundant eukaryotic taxa may be replaced by warmer adapted temperate species

197 s, in addition to Rh proteins, across insect taxa may indicate a conserved function for AMTs in sperm

198 all within the morphological range of extant taxa, Mesodescolea reveals unexpected early morphologica

199 but the details of how sea turtles and other taxa navigate during these migrations remains an open qu

200 emonstrated an intra-individual reduction of taxa number when compared to the skin surface.

201 We show that EAB-resistant taxa occur within three independent phylogenetic lineage

202 In this study, we identified 30 taxa of hitchhiking plant propagules on the air-intake g

203 acetic acid bacteria (LAB/AAB) and bacterial taxa of predicted environmental origin.

204 cles for nematodes, one of the most abundant taxa of the benthic meiofauna.

205 ssed for only two taxa, with the majority of taxa only having one or two criteria assessed.

206 abase design is ready to be applied to other taxa or biological processes.

207 will be necessary to decipher which specific taxa or metabolites drive CRC biology and to fully chara

208 hallenge is to test whether specific biomes, taxa or types of species benefit or suffer in a time of

209 ng a decrease in number and heterogeneity of taxa over the skin surface of MCT, at both inter- and in

210 microbial composition over time and only few taxa persisting across the 3 y of the study.

211 ean trade into reach for a greater number of taxa, places, and contexts.

212 gnore evolutionary relations among microbial taxa, potential relations between modulating factors, as

213 rprised that the reactors supported multiple taxa presumed to be autotrophic Fe(II) oxidizers based o

214 anzee guts were enriched in some of the same taxa prevalent in infant humans (e.g., Bifidobacterium,

215 Across all coral taxa, projected stochastic growth rates (lambda(s) ) wer

216 he diversity recovered; (6) the diversity of taxa recovered has shown this can be an important tool t

217 lated with the proliferation of several core taxa related with citrus health.

218 dominant, though the exact function of most taxa remains unclear.

219 er it mediates cell adhesion in non-metazoan taxa remains unknown.

220 rray of morphological diversity among animal taxa represents the product of millions of years of evol

221 ous nuclear-encoded proteins, for 157 and 76 taxa, respectively.

222 Some taxa respond to environmental change by increasing popul

223 s in thermoregulatory capacity in amphibious taxa sampled from across mammalian phylogenetic diversit

224 of the pectoral fins of 3 key tetrapodomorph taxa-Sauripterus taylori (Rhizodontida), Eusthenopteron

225 biota was enriched by the Th17 cell-inducing taxa segmented filamentous bacteria (SFB).

226 Both taxa segregate ON and OFF signals.

227 half of the 360 living species and 482 total taxa (species and subspecies combined) are threatened wi

228 Furthermore, the assay permitted detecting taxa-specific effects of surface water samples.

229 Changes in fecal bacteria were assessed by taxa-specific quantitative polymerase chain reaction and

230 Indicator species analyses identified taxa specifically associated with Campylobacter burden.

231 Using other vertebrate taxa, such as birds, can contribute to a more comprehens

232 ty and fragmented nature of genomes from key taxa, such as Porifera.

233 Specific viral taxa, such as Staphylococcus phages and Herpesviridae, w

234 ultrastructural features with Plagiostriata taxa, such as the presence of a sternum with parallel st

235 taxa, and it is unclear whether well-studied taxa, such as vertebrates, reflect changes in wider biod

236 bolic functions across different co-existing taxa supported functional redundancy and imparted proces

237 Empirical evidence from diverse eukaryotic taxa supports the mitonuclear compensatory coevolution h

238 As a result, cave-obligate taxa, termed troglobionts, are no longer viable on the s

239 emperature generally had stronger effects on taxa than changes in fish predation or trophic state med

240 sect communities, sometimes including insect taxa that are otherwise rare or absent.

241 obal climate change may detrimentally impact taxa that avoid low oxygen concentrations (Beroe, doliol

242 d seven taxa that produce butyrate and three taxa that degrade oxalate.

243 Amphibians were the only taxa that experienced net declines in the analysed data,

244 rived from observations across multiple fish taxa that live in low light environments and do not poss

245 hes that enable the co-existence of multiple taxa that occupy the same apparent metabolic niche when

246 oncentrations (Beroe, doliolids), but favour taxa that occur in the OMZ (Lilyopsis, phaeodarians, Cyd

247 OR = 0.28 (0.09-0.91), P = 0.034), bacterial taxa that predict butyrate production (OR = 0.38 (0.17-0

248 These included seven taxa that produce butyrate and three taxa that degrade o

249 We identified 11 Ascomycota taxa that were more highly enriched in moldy homes and 1

250 We identified 60 taxa that were significantly affected by nanopesticide e

251 ional taxonomic units), including many small taxa that would be undetected in traditional in situ sur

252 For other animal taxa, the current understanding of, and evidence for, cl

253 l relationships to reveal specific bacterial taxa, the dynamics of which are substantially perturbed

254 matic and ecologically important carnivorous taxa, the Felidae family.

255 merging pattern suggests that for some avian taxa, the ontogeny of migratory strategy is a prolonged,

256 Of these taxa, the spiny water flea (Bythotrephes longimanus) mos

257 Additionally, for both taxa, there was a significant positive correlation betwe

258 ations than is possible in studies of extant taxa, thereby integrating microevolutionary process and

259 With most of the world's Caprinae taxa threatened with extinction, the IUCN appeals to the

260 tribution of distinct copiotrophic bacterial taxa to carbon cycling.

261 d stronger, more consistent responses across taxa to land use than widely used metrics of species ric

262 ndividual-to-population-level impacts across taxa, trophic levels and biomes at a global scale.

263 rate adapted bacteria may replace cold water taxa under a future scenario of increasing Atlantic infl

264 tions of reconstructed trees (linking extant taxa) under the BD model in backward time, conditioned o

265 95% of the recovered MAGs represented novel taxa underscoring the limited representation of cultured

266 Although rare, several taxa use venom for agonistic intraspecific competition (

267 A subset of these taxa was associated with increased frailty in subjects f

268 ly of the so-called "problematic" Gonideinae taxa was supported by all the inferred phylogenies in th

269 sed on well-preserved ultrastructures of two taxa, we here propose new interpretations regarding both

270 omposition (P = .04), but no specific marker taxa were associated with response.

271 For example, abundances for most dominant taxa were at all-time lows since the beginning of sampli

272 iliating with previously described symbiotic taxa were detected but their detection was rare and not

273 Many individual bacterial taxa were differentially abundant (false-discovery rate,

274 Several taxa were enriched compared to IBS-D.

275 tial in vitro and the majority of beneficial taxa were harvested from well-growing plants.

276 ons of young (neo-) and old (paleo-) endemic taxa were identified using distribution data of 1719 gen

277 g bacterial taxa with a prevalence >0.1%, 31 taxa were less abundant among individuals with nephrolit

278 Differentially abundant taxa were linked to constipation, physical activity, pos

279 versity and abundances of specific bacterial taxa were quantified by sequencing 16S rRNA genes in fec

280 No individual taxa were significantly more abundant in either group.

281 tress periods, the observed dynamics for all taxa were unable to maintain current community compositi

282 accumulate the greatest diversity of insect taxa when they are widespread and show some resemblance

283 scribed here extend the number of vertebrate taxa where endogenous chitin production has been detecte

284 n only the longest established high-altitude taxa, whereas hexokinase activity increased in only newl

285 morphology between stem cetaceans and extant taxa, whereas its axial skeleton displays incipient rigi

286 the absolute levels of a shared group of 14 taxa (which are not typically classified as enteropathog

287 l availability of heathland fungal and plant taxa, which reinforce each other, can significantly stee

288 ors" of root canal infections and identified taxa whose virulence properties should be further explor

289 form a morpho-functional comparison of these taxa with 12 models corresponding to eight fossil homini

290 Among bacterial taxa with a prevalence >0.1%, 31 taxa were less abundant

291 from over 84,000 reactions and 60 different taxa with cross-references.

292 n their relative abundance and identified 13 taxa with disrupted rhythmicity in type 2 diabetes (T2D)

293 have only been generated across a handful of taxa with highly degenerate sex chromosomes.

294 Offspring ornamentation typically occurs in taxa with parental care, suggesting that selection arisi

295 The four monocotyledonous taxa with the highest number of seeds collected were ana

296 eal breakage always occurs at the midline in taxa with unfused conditions, further indicating that an

297 ological stasis in evolution has resulted in taxa with unusually high numbers of primitive characters

298 all five criteria are assessed for only two taxa, with the majority of taxa only having one or two c

299 xonomic diversity-including of low-abundance taxa-with better metagenome-assembled genomes, longer co

300 n to be addressed, even across hyper-diverse taxa within arthropods.