ライフサイエンスコーパス: assemblage

1 owth, resulting in higher variability in the assemblage.

2 oral change in the species' functional trait assemblage.

3 s bonebed represents a perimortem gregarious assemblage.

4 ion of birds versus mammals in the frugivore assemblage.

5 ten difficult in archaeological shell midden assemblages.

6 coexist in equilibrium with silicate mineral assemblages.

7 nd larger islands having more stable species assemblages.

8 distinct biogeographic histories and species assemblages.

9 n waters with diatom-dominated phytoplankton assemblages.

10 with each other and/or with natural plankton assemblages.

11 diles were important modifiers of these bone assemblages.

12 se only a small fraction of these sub-fossil assemblages.

13 ing may erode the safe harbors of vulnerable assemblages.

14 uenced by the phylogenetic structure of host assemblages.

15 gen ratio of the leaves also affected the FE assemblages.

16 roplastics colonization dynamics and species assemblages.

17 and the time-averaged accumulation of faunal assemblages.

18 ated pairs, a trend that continues in modern assemblages.

19 tween Paleogene and Neogene Asian anthropoid assemblages.

20 st habitats of both regions comprised unique assemblages.

21 s and taxonomic composition of the floristic assemblages.

22 richer and three-fold more abundant juvenile assemblages.

23 r investigating processes that shape species assemblages.

24 es in shaping coevolution within mutualistic assemblages.

25 l aragonite from archaeological shell midden assemblages.

26 m functioning or the associated invertebrate assemblages.

27 emblages from relatively intact eastern fish assemblages.

28 This diverse assemblage, 780,000 y old, reflects a varied plant diet,

29 In refractory giardiasis, assemblage A and B were found responsible in 4 and 6 cas

30 d that 17 (25%) Giardia isolates belonged to assemblage A, and 31 (43%) belonged to assemblage B.

31 iro, the majority of samples were related to assemblage A.

32 Assemblages A and B are detected in humans, but they are

33 ted persistent giardiasis, belonging to both assemblages A and B, after nitroimidazole.

34 Giardia genotypes are classified into 8 assemblages (A-H).

35 showed significant differences in eukaryotic assemblages according to pH class, mostly between low pH

36 entation of fractional size in demersal fish assemblages along a depth gradient in the deep sea.

37 ested this prediction in winter annual plant assemblages along an aridity gradient using multilevel s

38 ersity and compare response patterns of moth assemblages among three elevational gradients establishe

39 Polar assemblage and accumulation of ZitP and its effector pro

40 fossil accumulation was studied as a single assemblage and interpreted as a succession of several hu

41 xtreme drought triggered changes in the fish assemblage and subsequent anomalous hydrological conditi

42 inter-individual variability in both species assemblages and abundance profiles.

43 o consistent with the faunal and microfaunal assemblages and almost double the previous age estimates

44 ed effects, ranavirus drove declines of host assemblages and changed host community composition and s

45 unity changes into warm- and cold-associated assemblages and found that English bird communities have

46 he evolutionary histories of pre-disturbance assemblages and highlights the importance of evaluating

47 ing the diversity and composition of species assemblages and identifying underlying biotic and abioti

48 of PCD on the fate of natural phytoplankton assemblages and its role in aquatic biogeochemical cycle

49 Moreover, the distribution of bacterial assemblages and physicochemical properties in surface se

50 The metal-dominated mineral assemblages and reduced volatiles in large gem diamonds

51 thern California, resulting in novel species assemblages and shifts in functional composition, which

52 pointing to a tight correlation between ESTU assemblages and specific physico-chemical parameters.

53 e and documented relationships between these assemblages and the host's sex, social status and group

54 that can be drawn from archaeological stone assemblages and the origins of ritual sites.

55 hat these microhabitats host distinct fungal assemblages and therefore promote diversity.

56 of the spatial variability of juvenile fish assemblages and to help focus conservation efforts.

57 habitat corresponded to a variation in bird assemblages and traits, as represented by intact canopy

58 rphospace captured in a single Late Triassic assemblage, and we hypothesize that many of the "novel"

59 ions in structuring the CBD and PBD of snake assemblages, and determine the extent in which snake ass

60 the earliest directly dated Middle Stone Age assemblages, and its associated human remains are the ol

61 ure and species composition all varied among assemblages, and this variation could be explained by th

62 more elevationally stratified than temperate assemblages, and tropical species would be more elevatio

63 In contrast, moth assemblages appeared to be dominated by generalist speci

64 obiont and the processes governing microbial assemblage are not well documented.

65 ects of global environmental change on plant assemblages are expected to be a factor in determining h

66 article-associated and free-living bacterial assemblages are functionally different and that the inte

67 Reef coral assemblages are highly dynamic and subject to repeated d

68 the ecological consequences for stream fish assemblages are rarely quantified.

69 species and 9.8% of all species in the UK-1 assemblages are scientifically described and many are ra

70 rs likely that high-elevation temperate moth assemblages are strongly resilient to environmental chan

71 Our study suggests that moth assemblages are under threat from future climate change

72 We investigate meltwater microbial assemblages as they exit the GrIS from a large outlet gl

73 te comparisons across different ant-symbiont assemblages as well as across different types of ecologi

74 Using adult and juvenile material from this assemblage, as well as computed tomographic imaging, we

75 o predict change in Great Plains stream fish assemblages associated with groundwater pumping from the

76 After an intense drought in 2005, the assemblage assumed a different and fairly persistent tax

77 m-group ants are recovered as a paraphyletic assemblage at the base of modern lineages varying greatl

78 termine the assembly and dynamics of species assemblages at different spatiotemporal scales.

79 comes increasingly important in shaping moth assemblages at higher elevations.

80 ct from co-occurring species than species in assemblages at lower altitudes.

81 ed to assemblage A, and 31 (43%) belonged to assemblage B.

82 In this study, we examine microfossil assemblages before and after a known tropical cyclone ev

83 By quantifying bird and vegetation assemblages before and after the 2008 ice storm in China

84 trongly indicate a shift toward a novel fish assemblage between the late 1990s and 2000s.

85 Differentiation of parasite assemblages between formerly connected islands reflects

86 We found that similarity in herbivore assemblages between Inga species was correlated with sim

87 We found major changes in the island plant assemblages between the two periods, with native flora s

88 position and evolutionary history of species assemblages, but especially the tropics and ectotherms r

89 in response to global change, local species assemblages can change, setting the stage for new ecolog

90 ears to be an especially important driver of assemblage change with depth.

91 How have North Sea skate and shark assemblages changed since the early 20th century when bo

92 The earliest Middle Stone Age assemblages come from eastern and southern Africa but da

93 sponse to temperature shifts of a nitrifying assemblage composed of the same organisms found in the f

94 ncreased the total abundance and changed the assemblage composition of adult spiders and beetles.

95 At high elevations, the insect assemblages consisted largely of habitat generalists tha

96 s found in a grain that has a separate metal assemblage containing icosahedrite (Al63Cu24Fe13), curre

97 erval, thus halving the temporal gap between assemblages containing only dinosaur precursors and thos

98 gical techniques to a distinctive stone tool assemblage created by a non-human animal in the New Worl

99 ntribute to differences in X. muta microbial assemblages, demonstrating the importance of contemporan

100 Alternatively, making species assemblages depauperate may result in the loss of multif

101 In our study, juvenile fish assemblages differed between pristine arborescent forest

102 ere exchanged at sea or not, their bacterial assemblages differed from those of local, coastal water.

103 ionally the associated infaunal invertebrate assemblages differed, with significantly less polychaete

104 of modern and late Holocene plant and animal assemblages differs fundamentally from that of assemblag

105 -makes deciphering early archaeological bone assemblages difficult.

106 on phylogenetic structure of angiosperm tree assemblages distributed across a wide range of environme

107 Bacterial assemblage diversity in the PA fraction always exceeded

108 ng Cyclone Hamish, and discernible shifts in assemblage diversity.

109 y's sustainability is based on exploiting an assemblage dominated by species with life histories comb

110 Communities within flies were not random assemblages drawn from a common pool; instead, many bact

111 Detection of assemblage E in humans suggests a new zoonotic route of

112 Surprisingly, assemblage E was detected in 15 samples.

113 oral species; however the diversity of coral assemblages, environmental conditions, assessment protoc

114 Pleistocene human-associated archaeological assemblages exists, the scarcity of hominin fossils ofte

115 neutral processes in structuring ectothermic assemblages facing changes towards warmer and dryer clim

116 larly explained by spatial factors but snake assemblages facing dry summers are more affected by spat

117 ity of the decapods involved in exosymbiotic assemblages for juvenile and adult Pocillopora damicorni

118 ocks and for the interpretation of the phase assemblage found in Khatyrka.

119 taxa in the same assemblage (the Otis Chalk assemblage from the Dockum Group of Texas) demonstrate t

120 The present study examined 73 microbial assemblages from 25 individuals with generalized chronic

121 Through multivariate analyses of pollen assemblages from Lake El'gygytgyn, Russian Far East and

122 tions of each lake and depth; in particular, assemblages from layers beneath the chemocline had bioge

123 stem rivers isolate depauperate western fish assemblages from relatively intact eastern fish assembla

124 ased primarily on monospecific bedding plane assemblages from the Lower-Middle Devonian Kwataboahegan

125 sed on changes in sedimentary facies, fossil assemblages, geochemistry, and paleotemperature.

126 ented coral loss and homogenization of coral assemblages globally, we investigate the inherent struct

127 between Neandertals and this "transitional" assemblage has been controversial because of the lack ei

128 al fungi (AMF) and the rules that govern AMF assemblages has been hampered by a lack of data from nat

129 Even species within the same assemblage have varied responses to climate change, and

130 expensive-to-manufacture goods in household assemblages, have been proposed, the first is not clearl

131 This fossil assemblage, here named the Zuun-Arts biota, currently co

132 remains in highly fragmentary archaeological assemblages, improving the resources available for wider

133 Species assemblage in a local community is determined by the int

134 rence of these two pathogens in an amphibian assemblage in Serra da Estrela (Portugal).

135 ten a dominant component of the invertebrate assemblage in streams, and play a vital role in aquatic

136 of Neolithic pottery from an archaeological assemblage in Western Germany, and argue that the widely

137 used to monitor future changes to herbivore assemblages in a 'hotspot' of biodiversity.

138 , oxygen isotopes, and diatom and cladoceran assemblages in a sediment core from a freshwater lake on

139 d the composition and diversity of bacterial assemblages in ballast water from tanks of 17 commercial

140 netic diversity encountered at low-elevation assemblages in comparison to tropical geometrid communit

141 ur results thus suggest that coastal seaweed assemblages in eutrophic waters may undergo an initial s

142 eukaryote primers showed that core-cercozoan assemblages in faecal samples are as diverse as those fo

143 not allow extrapolations to novel community assemblages in future climates, which will require a mec

144 The results reveal similar palynomorph assemblages in limestones and marls.

145 f foraminifer shells and benthic foraminifer assemblages in marine sediments indicate that enhanced C

146 between the volatile compounds and bacterial assemblages in meerkat paste, particularly in males.

147 vealing the processes that structure species assemblages in natural communities.

148 he temporal activities and dynamics of viral assemblages in natural settings remain largely unexplore

149 s a mechanism that locally sculpts microbial assemblages in plant populations.

150 to intermediate spatial scale, whereas those assemblages in regions with rainy summers have a stronge

151 The metamorphic mineral assemblages in relatively FeO-rich Martian lavas can hol

152 ter while seawater harboured local bacterial assemblages in response to the Arctic hydrography.

153 terflies forming multiple coexisting mimicry assemblages in the Amazon.

154 d its role for the construction of bacterial assemblages in the Arctic Ocean.

155 ch geometrid moth (Lepidoptera: Geometridae) assemblages in the mature temperate forest on Changbai M

156 in the establishment of different bacterial assemblages in the root and rhizosphere.

157 000 years ago, with a distinctive stone tool assemblage including grinding stones, ground ochres, ref

158 onment as suggested by the co-existing plant assemblage including palms and golden rain trees among o

159 Mean trophic level of the assemblage increased modestly with decreasing biomass, c

160 tly change across reaction fronts separating assemblages indicative of incipient, intermittent, and f

161 Remarkably, we find that this assemblage interacts directly with at least eight differ

162 climate variability/change will affect these assemblages into the future.

163 gional and local scales with a prevalence of assemblages involving crab-shrimp partnerships.

164 y (CA-TIMS) U-Pb zircon ages reveal that the assemblage is early Carnian (early Late Triassic), 5- to

165 This novel assemblage is tightly linked to the warming temperatures

166 ock', but the behaviour responsible for this assemblage is unclear.

167 indicate that the structure of AMF community assemblages is correlated with P fertilization, soil dep

168 itation) in structuring tropical ectothermic assemblages is greater in regions with rainy summers whe

169 The outstanding feature of these assemblages is the overwhelming predominance of monothal

170 e structure adds to our understanding at the assemblage level.

171 Forecasting assemblage-level responses to climate change remains one

172 truct former population history and test for assemblage-level responses to cycles of moisture transpo

173 ncreased with depth at the intraspecific and assemblage levels.

174 Adaptations to differences in local prey assemblages may drive such divergence and, ultimately, s

175 ape scale, different herbivore densities and assemblages may result in dynamic gradients in woody cov

176 define two distinct niches and that epibiont assemblage might be driven in part by selective processe

177 Because predator assemblages might also influence the impact of large her

178 lished warning signals present in local prey assemblages, most are incompletely known to local predat

179 ion could be explained by the depth that the assemblage occupied.

180 A unique macrobotanical assemblage of 55 food plant taxa from the Acheulian site

181 hts include: (i) regio- and stereocontrolled assemblage of a pivotal (Z)-gamma-ylidene-beta-bromobute

182 duplicated genes, cells can orchestrate the assemblage of aaRSs oligomers that meet the necessities

183 , focusing on the diverse and self-contained assemblage of arthropods associated with an abundant Bra

184 ority of fleas were host-generalists but the assemblage of Bartonella variants in fleas tended to ref

185 ella variants in fleas tended to reflect the assemblage of Bartonella variants in the host species th

186 e rock sample from which this earliest known assemblage of cellular fossils was described more than t

187 Formation, which preserves a quintessential assemblage of dinosaurian precursors (early dinosauromor

188 h host species is associated with a distinct assemblage of genetic variants, indicating that between-

189 This finding suggests that stringent assemblage of Hsp90 keeps CRAF kinase equipped for parti

190 a more detailed investigation of the lithic assemblage of layer I.

191 notype colonization dynamics and the genetic assemblage of populations.

192 ings uncover a rich and functionally diverse assemblage of previously unknown proteins that regulate

193 tribution and occurrence of the elasmobranch assemblage of the southern North Sea, based on extensive

194 n the present study, we found that bacterial assemblage of the surface sediment was different from th

195 Island, Kenya, have uncovered a catastrophic assemblage of the wildebeest-like bovid Rusingoryx atopo

196 population of premotor interneurons, but the assemblage of this network remains incompletely understo

197 Here we report an assemblage of unusual sauropod tracks from the Lower Cre

198 s to climate-mediated effects on the species assemblages of an important fish nursery area.

199 Here, we analyzed 57 assemblages of angiosperm trees in 0.1-ha forest plots a

200 of hemosporidian lineages infecting similar assemblages of avian host species.

201 Mesocosm experiments conducted with natural assemblages of benthic macroinvertebrates established co

202 eistocene hominids rely mostly on very small assemblages of bony remains.

203 The community assemblages of EBLF could have been changing over time,

204 lly tractable, and that, for microscale cell assemblages of encapsulated marrow stromal cells culture

205 ogical process in coral reefs, where diverse assemblages of fish maintain reef health by controlling

206 opmental gene regulatory networks (GRNs) are assemblages of gene regulatory interactions that direct

207 to characterize long-term change in insular assemblages of hemosporidian parasites.

208 water limitation of photosynthesis in given assemblages of leaves).

209 rd of the K-Pg extinction based on extensive assemblages of marine macrofossils (primarily new data f

210 etic ecosystems are known to support diverse assemblages of microorganisms, the ecological and enviro

211 (respectively), with relatively depauperate assemblages of mostly small-bodied animals, than in the

212 Previously, assemblages of multiple and diverse types of Pleistocene

213 s can identify the factors governing complex assemblages of multiple hosts, parasites, and vectors, a

214 s frequently function as parts of complexes, assemblages of multiple proteins and other biomolecules,

215 f Nitrosopumilus, Nitrosotalea and different assemblages of Nitrososphaera (subcluster 1.1, and unass

216 On Earth, different assemblages of organic matter types are derived from var

217 s environmental conditions change, different assemblages of organisms are selected for, altering link

218 we devise methods that preserve the in vivo assemblages of SCF complexes and apply quantitative mass

219 an, but a residual ultimately drives diverse assemblages of seafloor heterotrophs.

220 lineages have been exposed to very different assemblages of seed-dispersing vertebrates.

221 assing over 11,000 species' responses for 54 assemblages of taxonomically related species occurring t

222 frican ape and human origins, but few fossil assemblages of this period have been reported from sub-S

223 We find that assemblages on formerly connected islands are as differe

224 The effects of predator assemblages on herbivores are predicted to depend critic

225 y connected islands are as differentiated as assemblages on islands that have never been connected, a

226 he collective vulnerability of species in an assemblage, or "assemblage vulnerability." We find that,

227 minence, little is known about this sailfish assemblage, or its relationship to other aggregation sit

228 limiting resources, our findings imply that assemblage organization in clumps should be a common fea

229 hat accumulated the bulk of biomass early in assemblage organization.

230 te rates of change in hemosporidian parasite assemblages over a millennial time frame.

231 semblages differs fundamentally from that of assemblages over the past 300 million years that predate

232 tigraphy, quantified results from the lithic assemblages, preliminary faunal remains analyses, geochr

233 tion sequencing, we identified the bacterial assemblages present in meerkat paste and documented rela

234 spp.), following bush encroachment, the new assemblages presented more potential opportunities for s

235 discovery of 1.5-million-year-old footprint assemblages, produced by 20+ Homo erectus individuals.

236 The specific mineral assemblage provides evidence for a moderate Hadean clima

237 The Leang Bulu Bettue assemblage provides insight into the complexity and dive

238 malous hydrological conditions have hampered assemblage recovery.

239 d homogenization of Great Plains stream fish assemblages related to groundwater pumping, and we predi

240 bsequent years following Hamish, the surface assemblage returns to its pre-cyclone form, but results

241 Viral gene transcription in host cell assemblages revealed diel cycling among many different v

242 and both are more differentiated than local assemblages sampled up to two decades apart.

243 ous (Hauterivian) ostracod and foraminiferal assemblages showing marked shallow-marine preferences.

244 ton, which may result in this ratio in algal assemblages similar to that in water column.

245 and filaments with morphologies and mineral assemblages similar to those of filamentous microorganis

246 Experimental warming consequently shifted assemblage size spectra in ways that were unexpected, bu

247 al protection on biomass and density of fish assemblages, some commercially important fishes, and sea

248 tructure of 359,896 unique taxon pairs in 80 assemblages spanning the past 300 million years.

249 revealed consistent transformations in fish assemblage structure among western subwatersheds with in

250 558 km of stream, and transformation of fish assemblage structure from dominance by large-stream to s

251 - and species-level traits into one succinct assemblage structure metric, fractional size, which is c

252 nd synchronous changes in hydrology and fish assemblage structure of a floodplain lake near the confl

253 warming experiment that shifted invertebrate assemblage structure via unanticipated mechanisms, while

254 Associated shifts in invertebrate assemblage structure were driven by the arrival of new t

255 oth structural (i.e. biomass, stoichiometry, assemblage structure) and functional (i.e. metabolism, N

256 uctions has been comparable for many insular assemblages, suggesting that introductions could have 'c

257 s are part of a freshwater vertebrate fossil assemblage that documents a period of extreme climatic w

258 and comprise the first sub-Saharan mammalian assemblage that spans this period.

259 information available on the microbiological assemblages that are associated with this vast and clima

260 We used studies of assemblages that directly compared geographic distributi

261 singly, numerous additional taxa in the same assemblage (the Otis Chalk assemblage from the Dockum Gr

262 of cold- vs. warm-adapted species in a local assemblage [the community temperature index (CTI)] with

263 aphic changes from analysis of foraminiferal assemblages, the abundance of ice-rafted debris, and sor

264 ng increasing biotic homogenization of avian assemblages throughout the United States.

265 Here, we used a natural diatom-bacterial assemblage to investigate the diversity and response of

266 the behaviour leading to artefacts and their assemblages to be incorporated.

267 be the first ever experiment to warm benthic assemblages to ecologically relevant levels in situ.

268 lex, but we demonstrate that the response of assemblages to elevated CO2 are correlated with inorgani

269 We used 218 snake assemblages to quantify the compositional (CBD) and phyl

270 ges, and determine the extent in which snake assemblages under distinct climatological regimes are af

271 bsence and relative abundance in larval fish assemblages until metabarcoding methods are optimized fo

272 iversity, and phylogenetic diversity of bird assemblages, using roadside monitoring data of the North

273 Among Cystoseira forests, juvenile assemblages varied through space (i.e. between localitie

274 r 35 islands across Northern Melanesia, bird assemblage vulnerability and biodiversity are positively

275 lnerability of species in an assemblage, or "assemblage vulnerability." We find that, for 35 islands

276 rs (66% of variance explained), but the rare assemblage was not (16%).

277 cellular and viral size fractions, the viral assemblage was remarkably stable, with the most abundant

278 ous studies, we observed that the non-native assemblage was surprisingly unresponsive to extreme even

279 ive and non-native species richness in local assemblages was found at the global scale, while regiona

280 sequencing analysis showed the heterogeneous assemblages were (1) dominated by Alpha- and Gammaproteo

281 Thus, these salt marsh and mangrove assemblages were accreting sediment and building vertica

282 Host bacterial and fungal assemblages were compared in tadpoles from the pond of o

283 Prokaryotic microbial assemblages were dominated by Proteobacteria, Bacteroide

284 Three major ESTU assemblages were identified along the cruise transect fo

285 ephalida is basal to the main scuticociliate assemblage, whereas the thigmotrichs are placed within t

286 nctionalization, created the current S locus assemblage which led to floral heteromorphy in Primula.

287 organic soil components to distinct mineral assemblages, which are in turn stabilized by biophysical

288 ronments generating a species-rich geometrid assemblage, while exclusion of phylogenetically closely

289 We predict that this assemblage will be responsive to projected increases in

290 n the formation of Oldowan zooarchaeological assemblages will only be accurately revealed by better b

291 icroarchitecture built of a definite mineral assemblage with various organic matter forms and a speci

292 dictor and response variables) of a seagrass assemblage with well-defined species interactions to oce

293 tained highly abundant and diverse bacterial assemblages with alginolytic potential, including member

294 Bryozoans form species-rich assemblages with other encrusting fauna and flora (corra

295 urs, such as forming transient multicellular assemblages with properties and adaptive abilities excee

296 ange shifts for a subset of 21 studies of 26 assemblages with sufficient data.

297 We observed massive impacts on a marine assemblage, with near doubling of growth rates of Antarc

298 factors best explain the structure of snake assemblages within a same climatological regime.

299 s, and the structure of invertebrate benthic assemblages would be influenced by microplastics.

300 We hypothesised that tropical assemblages would be more elevationally stratified than