ライフサイエンスコーパス: assemblage

1 ith the seasonal impact of the EAC microbial assemblage.

2 e genetic diversity across the regional frog assemblage.

3 of thermal stress within a subtropical coral assemblage.

4 e the genetic diversity of the regional frog assemblage.

5 rcentile of ~ 14 kg to only ~ 4 kg in modern assemblages.

6 our theory may be applicable to more-complex assemblages.

7 enic activities, thus influencing associated assemblages.

8 ideo transects were used to sample reef fish assemblages.

9 novel-functions relative to preextinction LP assemblages.

10 ic and terrestrial factors structuring these assemblages.

11 rally prevailed with relatively few distinct assemblages.

12 stic GH profiles matching distinct microbial assemblages.

13 the effects of coral morphology on reef fish assemblages.

14 covering complete virus genomes from natural assemblages.

15 similar to those of the LP than native-only assemblages.

16 ated to climatic conditions on the scavenger assemblages.

17 ying and protecting the uniqueness of biotic assemblages.

18 enotype was associated with diverse effector assemblages.

19 bance and restoring framework building coral assemblages.

20 nmental drivers on the ecology of reef coral assemblages.

21 inerals, or lack of equilibration of mineral assemblages.

22 y jeopardise the persistence of such diverse assemblages.

23 ifferent, respectively, compared with modern assemblages.

24 ctional diversity present in coral reef fish assemblages.

25 nisms can simultaneously structure community assemblages.

26 hion willow), a common component of subnival assemblages.

27 ly comprise upslope shifts of modern lowland assemblages.

28 dom been shown and explained in multispecies assemblages.

29 much larger than those from skeletal fossil assemblages.

30 ature variation is smaller in high elevation assemblages.

31 hich is particularly true for mature biofilm assemblages.

32 ifferent (deeper) previously altered mineral assemblages.

33 that persist in simulations of multispecies assemblages.

34 BEF relationships, in natural high-diversity assemblages.

35 processes for species richness in individual assemblages.

36 t of the prevailing forces structuring those assemblages.

37 urrent ecosystems and the emergence of novel assemblages(1-3).

38 nsional phosphatic replicates in Orsten-type assemblages [4, 17-19] or as "small carbonaceous fossils

39 ity between the two human-pathogenic genetic assemblages (A and B) of the parasite.

40 ugh Dolly Varden were a minority (29% of the assemblage), a sign of some fitness difference.

41 al communities are partitioned into distinct assemblages across a gradient of Atlantic-Polar Water in

42 tion in the composition of macroinvertebrate assemblages across climates and continents, respectively

43 s study, the evolution of ballast water (BW) assemblages across different trophic levels was characte

44 calculated a local defaunation index for all assemblages-adjusted by a false-absence ratio-which was

45 ifts in the morphological structure of coral assemblages affect the abundance of juvenile and adult r

46 composition varied during night activity in assemblages along gradients of local and landscape envir

47 The concurrent export of microbial assemblages alongside glacial meltwater is expected to i

48 in situ division rates for the picoeukaryote assemblage and compared the dynamics with those of the p

49 Here we present a sedimentary diatom assemblage and diatom isotope dataset from Schrader Pond

50 gy, isotopy), we interpret the origin of the assemblage and diverse paleobiological and paleoecologic

51 Therefore, secretory pathway-mediated assemblage and excretion of infective particles represen

52 Here, we present detailed faunal assemblage and taphonomic data from Fa-Hien Lena Cave in

53 Here we analyse 6,801 ecological assemblages and 376 host species worldwide, controlling

54 We surveyed fish assemblages and deployed macroalgal assays within macroa

55 he Great Basin, a cold desert, have distinct assemblages and meet along a contiguous, east-west bound

56 ming practices may have consequences on fish assemblages and the ecological functions performed, thus

57 nsitions may influence bees, we compared bee assemblages and their seasonality among sites at the Sev

58 redundancy and complementarity of pollinator assemblages and, therefore, might alter the performance

59 y equivalent species are small in this local assemblage, and balanced by resource partitioning, a mod

60 including surface accessible atoms, overall assemblage, and interactions among the molecules of DOM

61 is ubiquitous in multi-host, multi-parasite assemblages, and can have profound implications for ecol

62 kton were inoculated with seawater bacterial assemblages, and communities were transferred daily to m

63 beds in terms of habitat heterogeneity, fish assemblages, and herbivory.

64 the landscape, strongly influencing the way assemblages are distributed.

65 undance of morphological groups within coral assemblages are likely to affect population replenishmen

66 nic matter decomposition, although how local assemblages are responding to climate change and whether

67 t with the thermal melanism theory, mushroom assemblages are significantly darker in areas with cold

68 Subtropical coral assemblages are threatened by similar extreme thermal st

69 ncluding an Initial Upper Palaeolithic (IUP) assemblage argued to represent the earliest arrival of U

70 project that future disruption of ecological assemblages as a result of climate change will be abrupt

71 Conflicting concepts which assume assemblages as either sharply delineated communities or

72 the magnitude of warming, threatening 15% of assemblages at 4 degrees C, with similar levels of risk

73 ration, which limits the colour diversity of assemblages at high elevations.

74 y and composition of cryptic coralline algal assemblages at sites that differ in urchin biomass and k

75 mammals constitute an important part of this assemblage because not only do they represent the first

76 zones of North and South America, with those assemblages becoming enveloped by assemblages from the s

77 ze the need for long-term monitoring of fish assemblages before and after dam construction in order t

78 Restructuring of wildlife and livestock assemblages (both in terms of species diversity and comp

79 It also resulted in a dissimilar microbial assemblage (Bray-Curtis Index, PERMANOVA, F = 2.2063; R(

80 ty effects altered the structure of parasite assemblages, but this effect depended on host genotype,

81 Under RCP2.6, predicted changes to ant assemblages by 2100 are moderate.

82 potential for radical change to montane ant assemblages by the end of the 21st century if temperatur

83 unctions and the composition of invertebrate assemblages, by comparing invertebrate diversity and soi

84 However, it is unknown how airborne pollen assemblages change across time and space.

85 Snow assemblages changed markedly throughout the sample perio

86 This variety results in distinctive gene assemblages characterising each state.

87 ed specific characteristics of EAC microbial assemblages compared with non-EAC assemblages, including

88 In this work, we analyze an assemblage composed of 13 individuals of different ontog

89 hat future state transitions could alter bee assemblage composition in our system.

90 al large-scale, synchronized ichthyoplankton assemblage composition shifts during past major climate

91 emains in lake sediments revealed changes in assemblage composition that coincided with the initial a

92 ce were 4.2% and 2% lower, respectively, and assemblage composition was altered at sites with an abru

93 proxy for deformation in a network of diatom assemblages comprising 452 species in 273 lakes across C

94 uences) from 147 infracommunities (i.e., the assemblage consisting of all mites of different species

95 Thirteen distinctly different molecular assemblages containing 4-, 5-, or 6-coordinate Si center

96 the most species-rich and complex vertebrate assemblages, coral reef fishes, within a large-scale phy

97 Critically, we predict that future assemblages could be reorganized in terms of which speci

98 brate composition, suggesting that microbial assemblages could be used to establish biotic criteria f

99 Cells in assemblages differentiate and perform distinct roles.

100 Here, we develop a new approach based on assemblage dispersion fields, formed by overlaying the g

101 In general, the two fungal assemblages displayed high diversity, richness, and domi

102 By influencing the biology of assemblages, disturbance can thereby stimulate change in

103 imate-driven species redistribution on local assemblage diversity remain unknown.

104 to, and potentially maintain, broader-scale (assemblage) diversity in regions that contain mixtures o

105 aracterized by distinct hydrography and prey assemblages during migration, similar to breeding adults

106 Six nasal airway microbiota assemblages, each dominated by Moraxella, Staphylococcus

107 hat, independent of latitude, high-elevation assemblages emerge as exceptionally susceptible to funct

108 ong pollinators' phenologies within European assemblages, except in the most northeastern part of Eur

109 Under RCP8.5, however, highland assemblages face almost a tripling of species richness a

110 cts, quantitative analysis suggests the BD 1 assemblage fits more closely with the variability previo

111 mily proteins in type II polyketide synthase assemblages for maintaining biosynthetic pathway fidelit

112 y, richness, and dominance indices, with the assemblage found in snow having the highest diversity in

113 Here we describe an archaeological assemblage from Chagyrskaya Cave, situated in the Altai

114 y dated (mid-eighth century to 818 CE) glass assemblage from the Rabad of Saqunda in Cordoba, capital

115 emporal shifts in populations and ecological assemblages from 6090 globally distributed time series a

116 tinctive toolkit closely resembles Micoquian assemblages from central and eastern Europe, including t

117 s is unknown before the 2.58-2.55 Ma Oldowan assemblages from Gona, Ethiopia.

118 stratified and directly dated archaeofaunal assemblages from Mongolia's early pastoral cultures to u

119 try from Dhaba strongly resembles stone tool assemblages from the African Middle Stone Age (MSA) and

120 These three lizard track assemblages from the Korean Cretaceous constitute the en

121 with those assemblages becoming enveloped by assemblages from the subtropics.

122 his latitudinal and elevational variation in assemblage functional structure is underpinned by nuance

123 The niche space occupied by local assemblages (functional richness) and dispersion in trai

124 g is kept below 2 degrees C, less than 2% of assemblages globally are projected to undergo abrupt exp

125 past continues to influence present species assemblages globally.

126 ensional feature vector, we find that within-assemblage image feature variation is smaller in high el

127 We found that variation in endophyte assemblages in above-ground tissues varied with host gro

128 ce, species richness, diversity, and species assemblages in both the floral plantings and adjoining a

129 Macroinvertebrate assemblages in depressional wetlands may be especially s

130 We argue that the composition of vertebrate assemblages in ecotone regions of forest-savanna transit

131 canopy and understory were twice as dark as assemblages in ground and subterranean strata.

132 Scavenger assemblages in highly human-impacted areas sustained the

133 iated with ecological processes to show that assemblages in highly urbanised environments have substa

134 tures preserved among frond-dominated fossil assemblages in Newfoundland (Canada).

135 ough cycles of glaciation, leading to unique assemblages in polar waters, rather than being entirely

136 g metabarcoding and microfossil foraminifera assemblages in sediment cores taken off Newfoundland acr

137 We show that assemblages in the Arabian Gulf are half as diverse and

138 t assemblages was vertically stratified: ant assemblages in the canopy and understory were twice as d

139 d proliferation of amniote-dominated dryland assemblages in the east.

140 tor for selective engagement with hyaluronan assemblages in the glycocalyx that are large enough to c

141 r to each other (at the family level), while assemblages in the North and South American temperate we

142 We investigated 39 anuran assemblages in the Pantanal wetlands (Brazil) with passi

143 also examined temporal changes in cladoceran assemblages in the sediments of two small lakes on the C

144 urveys, we analyzed temporal changes in fish assemblages in the Yangtze River upstream of the Three G

145 ch are subject to intense grazing, coralline assemblages in these urchin barrens are significantly le

146 Here we study haplochromine cichlid assemblages in two African Great Lakes to test these hyp

147 Assemblages in warm tropical lowlands and cold temperate

148 es level and pooled into cold- and warm-edge assemblages-in a multi-decade time-series of trawl surve

149 Nonribosomal peptides are assemblages, including antibiotics, of canonical amino a

150 microbial assemblages compared with non-EAC assemblages, including strain transitions within the SAR

151 nts, whereas Streptococcus species-dominated assemblages increased the risk of rhinovirus infection.

152 Several clades within the Yangshan assemblage independently evolved domain permutation in t

153 lisation propagates change through the plant assemblage into the plant-flower-visitor, plant-leaf min

154 environment resulted in the flushing of soil assemblages into the riverine system.

155 lion years ago and, consequently, its biotic assemblage is relatively young and derived from both col

156 The assemblage is taxonomically depauperate but includes fos

157 The 719-member-strong Yangshan virus assemblage is the sister clade to the expansive class Al

158 shment of biomass through cryptobenthic fish assemblages is greatly reduced on Earth's hottest coral

159 Currently, the source of exported assemblages is poorly understood, yet this information m

160 lucidation of similar processes in bacterial assemblages is recent and ongoing.

161 test whether the color lightness of mushroom assemblages is related to climate using a dataset of 3.2

162 shifts and their consequences on pollinator assemblages is still lacking.

163 regimes have been assessed at the species or assemblage level, whereas higher-level ecological networ

164 Temporal lags in population- and assemblage-level shifts after forest loss extended up to

165 Here, using assemblage-level tracking of marine predators, we identi

166 ypothesize that a large fraction of the fish assemblage may conduct seasonal migrations in this regio

167 y be caused by the use of different metrics: assemblage metrics may average out drastic changes in in

168 lations monitored individually, versus whole-assemblage monitoring.

169 The BD 1 assemblage, near the origin of our genus, provides a lin

170 The fossil assemblage notably includes many plant taxa that associa

171 The extensive IUP assemblage, now associated with directly dated H. sapien

172 t and bacterial DNA in fecal samples from an assemblage of 33 sympatric large-herbivore species (27 n

173 e and were replaced by a virtually monotypic assemblage of a smaller-sized, opportunistic species.

174 This specimen adds to a growing assemblage of Chinese Jurassic non-sauropodan sauropodom

175 vian-borne bacterial genes are shaped by the assemblage of co-existing avian, livestock and human com

176 ere incubated in seawater containing a mixed assemblage of cultured microalgae (control), with the ad

177 to how different processes contribute to the assemblage of ecological systems at different levels of

178 ng, yet our understanding of how its diverse assemblage of endemic species will respond is incomplete

179 The site represents the largest assemblage of footprints currently known from the human

180 th the most rapid advances occurring with an assemblage of larger-bodied shorter-distance migrants.

181 A newly discovered assemblage of lizard tracks from the Lower Cretaceous Ji

182 On the (010) surface, we find a rich assemblage of metallic states with two-dimensional dispe

183 The microbiome is an assemblage of microorganisms living in association with

184 Chagasic patients presented a diverse assemblage of parasite haplotypes covering TcI, TcII, Tc

185 have begun their evolutionary odyssey as an assemblage of RNA "fragments" smaller than the contempor

186 s predicted to have once supported a similar assemblage of species and are found within both intact r

187 ally on the little-known Succulent Biome, an assemblage of succulent-rich, grass-poor, seasonally dry

188 Here, we describe a substantial assemblage of systematically flaked stone tools excavate

189 ence of Levallois technology from the lithic assemblage of the Guanyindong Cave site in southwest Chi

190 he Late Pleistocene (38.4-13.5 ka) mammalian assemblage of the Tam Hay Marklot (THM) cave in northeas

191 Central to the assemblage of their underlying Aspidosperma skeleton is

192 molecular exchange is allowed within a large assemblage of van der Waals solids that are hydrogen-ric

193 acts upon the diversity, density and species assemblage of wildlife, livestock and humans.

194 soils contain unexpectedly diverse and rich assemblages of Bacteria and Eukarya indicating that ther

195 ily visualize metabolites made by very small assemblages of bacterial cells and that even these small

196 Here, using remote assemblages of coral reef fishes, we demonstrate strong,

197 ) and temporal (across 3 years) variation in assemblages of emergent dragonflies (Anisoptera) and ass

198 Based on resurvey data for seven assemblages of geometrid moths (>8000 individuals) on Mt

199 nduced efficiently by the large cross-linked assemblages of glycosaminoglycan present within leukocyt

200 Animal groups are heterogeneous assemblages of individuals with differing fitness intere

201 These attributes include assemblages of interconnected centers called the central

202 biofilms: highly ordered, surface-associated assemblages of microbes embedded in an extracellular mat

203 Late Cretaceous dinosaur assemblages of North America-characterized by gigantic t

204 istinct types of photoreceptive units (e.g., assemblages of photoreceptor cells).

205 ned how the amylolytic rate of combinatorial assemblages of six starch-degrading soil bacteria depend

206 ual) migratory behaviours in a deep-sea fish assemblage on the West African margin and, if so, identi

207 orphological makeup of habitat-forming coral assemblages on the Great Barrier Reef (GBR).

208 mentarity on the structuring of these anuran assemblages over fine-temporal scales.

209 ve group for addressing how diverse predator assemblages partition available prey resources.

210 Additionally, fish assemblage patterns and herbivory were not consistent ac

211 t which point horses come to dominate ritual assemblages, play a key role in pastoral diets, and grea

212 and the biological features of the streambed assemblage (Prokaryota, Protozoa and Eumetazoa invertebr

213 Changes in supraglacial meltwater assemblages reflected the transition of the glacial surf

214 ice brine and that they form a snow-specific assemblage reflecting the particular environmental condi

215 gs support that persistence of host-parasite assemblages reflects capacities of parasites to utilize

216 Our analysis indicated fish assemblage regime shifts in the two closer reaches in 20

217 fects on the diversity and structure of fish assemblages remain unclear.

218 e Nucleo-Cytoplasmic Large DNA Virus (NCLDV) assemblage represent a remarkably diverse and potentiall

219 ng the consequences of global change for bee assemblages requires accounting for both within-year and

220 cent (2014-2016) MHW and how ichthyoplankton assemblages responded to past major climate perturbation

221 sponses may better reflect the complexity of assemblage responses to land use development.

222 s are often coinfected with diverse parasite assemblages, resulting in complex interactions among par

223 Assemblage richness is not changing on average, although

224 We evaluated whether the severity of assemblage-scale and genus-level bleaching responses was

225 The severity of assemblage-scale bleaching responses was poorly explaine

226 he proportion of dead diatoms and the diatom assemblage sedimentation rate.

227 Pacific can help elucidate the magnitude of assemblage shifts, and whether responses are synchronous

228 addition, the microfossil and metabarcoding assemblages showed a congruent pattern indicating that p

229 Sampled assemblages showed evidence of being biologically connec

230 While mesocosm assemblages showed some compositional differences to sur

231 soils-despite large differences in herbivore assemblage size across years.

232 gical and metric variation in the Indonesian assemblage, some robust specimens, such as the partial m

233 ,000: "Using more than 18,000 flakes from 81 assemblages spanning two million years..." and "We appli

234 mperature change, we calculated species- and assemblage-specific sea bottom and sea surface temperatu

235 so, we contrasted aquatic-macroinvertebrate assemblage structure (family level) between subtropical

236 light of the substantial shifts in microbial assemblage structure and function associated with the EA

237 on of ants based on cuticle colour, altering assemblage structure and potentially ecosystem functioni

238 ork parameters can track the loss of aquatic assemblage structure in lakes associated with human pres

239 we examine differences in organismal traits, assemblage structure, and productivity of cryptobenthic

240 s, point to climate-driven simplification of assemblage structures and progressive homogenisation of

241 t in the homogenization of macroinvertebrate assemblage structures in temperate zones of North and So

242 We found that macroinvertebrate assemblage structures in the subtropical depressional we

243 riate dispersion indicated that family-level assemblage structures were more homogeneous in wetlands

244 f physiologically different cells in complex assemblages, such as in microbiome samples.

245 ation of calling activity in tropical anuran assemblages suggest potential trade-offs mediated by fin

246 Traits analysis of mesocosm assemblages suggested biodiversity loss was driven by de

247 na in compositions of some natural tilleyite assemblages, suggests that post-tilleyite structure has

248 We compiled 1,029 contemporary mammal assemblages surveyed across the Neotropics to quantify t

249 widespread declines from population surveys, assemblage surveys reveal a mix of declines and increase

250 As species-rich assemblages tend to be more functional, we warn about po

251 l stage had a greater influence in community assemblage than host taxonomy or locality.

252 produced an exceptional pig-dominated faunal assemblage that also contained a barbary macaque skull.

253 itional Moreno Hill (that is, Zuni) dinosaur assemblage that includes dinosaur groups that became rar

254 nderstanding these dynamics is the microbial assemblage that inhabits the cup-shaped leaves of the pi

255 Formation, 609 Ma old) is a rich microfossil assemblage that preserves biological structure to a subc

256 ence and species abundances) of all possible assemblages that can be formed from a given pool of spec

257 us from Dmanisi (Georgia)(1), two key fossil assemblages that have a central role in models of Pleist

258 anges and colonize new sites, creating novel assemblages that have historically not interacted.

259 stralian Current (EAC), transports microbial assemblages that maintain tropical and oligotrophic (k-s

260 ity-level body-size changes in tropical moth assemblages that moved uphill during a period of warming

261 abrupt, because within any given ecological assemblage the exposure of most species to climate condi

262 iving the persistence of scleractinian coral assemblages-the foundation species of coral reef ecosyst

263 chemical contamination on macroinvertebrate assemblages through this type of indicator.

264 New world army ants live in species-rich assemblages throughout the Neotropics and are voracious

265 rate in mediating their respective community assemblages, thus providing a better understanding of th

266 abundance from 21,500 terrestrial and marine assemblage time series across temperate regions (23.5-60

267 of 19,849 years Cal BP allows assigning this assemblage to a period of the MIS (Marine Isotope Stage)

268 nt the largest known Neandertal ichnological assemblage to date.

269 We used Illumina amplicon sequencing fungal assemblages to evaluate effects of nine treatments, each

270 ven-year assessment of the responses of fish assemblages to hypersaline discharge from the large Sydn

271 nses of soil bacterial communities and viral assemblages to stimulated anaerobic Fe(III)-bioreduction

272 nce the abundance and diversity of microbial assemblages transported downstream.

273 global data on habitat condition and species assemblage turnover to identify Earth's high-value biodi

274 Both assemblage types appeared to be highly resilient, re-est

275 cale as assumed by ecologic models; instead, assemblages undergo restructuring and extinction once lo

276 nificant evidence for a global, cosmopolitan assemblage unique to terminal Ediacaran strata.

277 data demonstrate that there was a microbial assemblage unique to the coral-turf algae interface disp

278 Nocturnal calling activity of anuran assemblages varied more within the 1-hr resolution than

279 Evidence suggests that the assemblage was formed by a local single event of catastr

280 We found that cuticle lightness of ant assemblages was vertically stratified: ant assemblages i

281 f 23 241 populations, 16 009 species, in 158 assemblages, we detected significantly accelerating exti

282 e sources can accumulate in freshwater algal assemblages, we hypothesized that nanoparticles may affe

283 body size for each species and calculated an assemblage-weighted mean for cuticle lightness and body

284 was lower in protected areas where predator assemblages were also more diverse, and that across all

285 The assemblages were dominated by cold-adapted and cosmopoli

286 ion years shows that ancient large-herbivore assemblages were functionally distinct from those that e

287 prising 43 sites, where vertebrate scavenger assemblages were identified using 2,485 carcasses monito

288 Temporal changes in the connected assemblages were similarly observed.

289 ter understand how wetland macroinvertebrate assemblages were structured according to geography and c

290 Microbial communities, including viral assemblages, were investigated after 60 days of Fe(III)-

291 vulnerability of polar associated community assemblages, which may change, impacting the ecosystem s

292 ial vertebrate scavenger (carrion-consuming) assemblages, which provide key ecosystem functions and s

293 Assemblage-wide mammal body mass distribution was greatl

294 affected by eutrophication, algal community assemblages will change, leading to variations in the na

295 e common and which are rare: future highland assemblages will not simply comprise upslope shifts of m

296 omplete characterisation of the trace fossil assemblage with additional ichnological properties such

297 Analysis of trait space overlap reveals that assemblages with introduced species are overall more sim

298 er avifauna was distinct from other Mesozoic assemblages, with amber entrapment including representat

299 have yielded rich Mesolithic archaeological assemblages, with one of the most iconic artefacts being

300 r from the Daptocephalus to the Lystrosaurus Assemblage Zone (AZ; Karoo Basin, South Africa) is time