ライフサイエンスコーパス: biogeography

1 n species distribution leading to changes in biogeography.

2 scape genetics under the more general field: biogeography.

3 nutrient availability to control microbiota biogeography.

4 ities is one of the most difficult issues in biogeography.

5 oor sediments may have distinctive bacterial biogeography.

6 for example, in mutation rates or historical biogeography.

7 or process-based modeling approaches to tree biogeography.

8 s Longqi in an Indian Ocean province of vent biogeography.

9 oceanic islands is a central theme of island biogeography.

10 ogists since Darwin's earliest insights into biogeography.

11 inferences of terrestrialization history and biogeography.

12 ic evolution, divergence time estimation and biogeography.

13 limits is a promising approach in functional biogeography.

14 sights into their life history evolution and biogeography.

15 e spatial scales for understanding microbial biogeography.

16 plotypes challenge predictions of vicariance biogeography.

17 /Pg)] mass extinction persist in present-day biogeography.

18 ty gradients dates back to the foundation of biogeography.

19 inferences about their ancestry and historic biogeography.

20 into marine actinobacterial biodiversity and biogeography.

21 biogeological functioning, biodiversity, and biogeography.

22 d with a focus on taxonomy, collections, and biogeography.

23 y reversing the classical scenario of oscine biogeography.

24 need to understand how climate is linked to biogeography.

25 t case for examining bacterial diversity and biogeography.

26 s the subjects of bacterial biodiversity and biogeography.

27 interpreting patterns of macroevolution and biogeography.

28 erstanding of placental mammal evolution and biogeography.

29 ndangered, still little is known about their biogeography.

30 ion are considered primary drivers of global biogeography.

31 tion belt, thereby laying the foundations of biogeography.

32 ally remains an open question in ecology and biogeography.

33 climate can confound insights into endophyte biogeography.

34 development of theories of biodiversity and biogeography.

35 solved questions in evolutionary biology and biogeography.

36 ts had an important early influence on their biogeography.

37 , key questions related to the ecology(4,5), biogeography(3,6,7) and divergence times(1,8-10) of ance

38 bining the theoretical foundations of island biogeography(7,8) with the temporal information containe

39 ter understand the factors controlling their biogeography, a reference database of the high-resolutio

40 role in shaping Bahamian hutia diversity and biogeography across islands.

41 efforts to characterize phage diversity and biogeography across various spatial and temporal scales.

42 es and describe the antimicrobial resistance biogeography along the intestine.

43 Additionally, distinct historical biogeographies and diversification patterns have led to

44 volutionary theory, including his studies of biogeography and animal breeding, and his recognition of

45 s revealed a strong correlation between host biogeography and bacterial diversity despite years of la

46 sult challenges a central paradigm in island biogeography and changes our perception of the relative

47 ming of shifts in climatic distributions and biogeography and compared these estimates to independent

48 Recent methods in historical biogeography and diversification rate inference were the

49 ed to the neuston but are poorly studied for biogeography and diversity.

50 unctional biogeography bridges species-based biogeography and earth science to provide ideas and tool

51 ystem and landscape management, restoration, biogeography and earth system modelling.

52 on patterns may be explained as artifacts of biogeography and ecological specificity.

53 However, little is known about their biogeography and ecology in the ocean.

54 n the global mid-ocean ridge system, but the biogeography and ecology of its hydrothermal vent fauna

55 al drivers of increased brain size including biogeography and ecology.

56 nities have the potential to influence plant biogeography and ecosystem function through their influe

57 and provide a framework for interpreting the biogeography and evolutionary history of tyrannosauroids

58 s the promise of admixture-based methods for biogeography and has ramifications for genetic ancestry

59 s revealing functional relationships between biogeography and health, particularly in the vertebrate

60 tracking, and defines the dual influence of biogeography and individuality on microbial composition

61 Biogeography and individuality shape the structural and

62 can influence viral distribution in light of biogeography and metacommunity ecology paradigms.

63 undations for continued investigation of the biogeography and molecular ecology of isoprene-degrading

64 Inferences from biogeography and molecular sequence data (but see ref.

65 ns with implications for contemporary island biogeography and our understanding of plant invasions.

66 Anthropogenic climate change has shifted the biogeography and phenology of many terrestrial and marin

67 The general concordance between biogeography and phylogeography indicates that the popul

68 indicating interspecific concordance between biogeography and phylogeography.

69 providing intraspecific concordance between biogeography and phylogeography.

70 tool for investigating historical aspects of biogeography and population genetic structure.

71 atyrrhines) is influenced by both historical biogeography and productivity but not by tree species ri

72 ar densovirus discovered, by documenting its biogeography and putative tissue tropism.

73 Dinoflagellate biogeography and sea surface temperature paleothermometr

74 erns are modified by underlying gradients in biogeography and species' ecology.

75 tes in healthy humans demonstrate that local biogeography and strong individuality define the skin mi

76 l oceanography in structuring benthic marine biogeography and suggest that a few environmental variab

77 e our ability to understand plant functional biogeography and the drivers of variation in plant and e

78 es distributions, thereby influencing future biogeography and the functioning of marine ecosystems.

79 uld be a valuable tool to investigate fungal biogeography and the host-pathogen interactions in bat W

80 o address this question, we investigated the biogeography and trajectories of biome and growth form e

81 diverse research in regeneration, symbiosis, biogeography, and aging.

82 interactions, community ecology, historical biogeography, and conservation biology.

83 einterpreting sloth morphological evolution, biogeography, and diversification history.

84 standing population dynamics, evolution, and biogeography, and for designing conservation actions.

85 s raise questions about their relationships, biogeography, and fossil record quality.

86 es of microbiome-related disease, diversity, biogeography, and molecular function.

87 s gut bacteria and how changes in intestinal biogeography are connected to inflammation.

88 Studies of biogeography are important for understanding biodiversit

89 and environmental factors that shape fungal biogeography are incompletely understood.

90 A set of postulates is proposed for biogeography as a guide to determining whether prokaryot

91 Island biogeography as applied to communities separated by time

92 This process is referred to in biogeography as vicariance.

93 dvance our general understanding of Malagasy biogeography, as aye-ayes have the largest species distr

94 The theory of island biogeography asserts that an island or a local community

95 ualized as an analog of the theory of island biogeography, assuming that plant species are islands se

96 ugia were characteristic features of ice-age biogeography at high latitudes.

97 t is an ideal habitat for studying microbial biogeography because of the dispersal issues involved.

98 Areas of endemism are important in biogeography because they capture facets of biodiversity

99 epresent ideal natural laboratories to study biogeography because they offer a discrete temporal and

100 agellate taxa and project changes in species biogeography between mean historical (1951-2000) and fut

101 With respect to biogeography, BPH ranges have expanded by 13% from 1992

102 plants and is a good model for investigating biogeography, breeding systems, coevolution with symbion

103 We show how functional biogeography bridges species-based biogeography and eart

104 level change also impacts terrestrial island biogeography, but it remains a challenge to evidence how

105 thern Ocean represent a new province of vent biogeography, but the spatial dynamics of their distinct

106 ial cycles, valuable models for evolutionary biogeography can be formulated.

107 We show how functional biogeography can provide important insights into the rel

108 In contrast, theories of biogeography, colonization, optimal foraging, and niche

109 eractions will be expressed through changing biogeography, community structure and adaptive evolution

110 enerated an emergent community structure and biogeography consistent with observed global phytoplankt

111 We anticipate that as trait-based biogeography continues to evolve, micro- and macroorgani

112 tions suggests that changing tree and forest biogeography could substantially lag habitat shifts alre

113 We review the biogeography, currently known limits of life, and molecu

114 By combining biogeography, ecology and evolution, our approach opens

115 and interpretation of ISARs as a tool within biogeography, ecology, and conservation.

116 ine interactive map for additional detail on biogeography, environmental microbiology, and exemplary

117 ce how sea-level rise impacts aquatic island biogeography, especially in the subterranean realm.

118 llary information (e.g. ecoregion, taxonomy, biogeography, etc.) that facilitates interpretation of t

119 ities) constitute a cornerstone for ecology, biogeography, evolution and conservation biology.

120 lithology must be considered for explaining biogeography, evolution, local extirpation or complete e

121 ble and efficient in addressing questions in biogeography, evolution, taxonomy and conservation of th

122 se distinct bacterial communities across gut biogeographies exhibit divergent behaviours is largely u

123 ntial being the equilibrium theory of island biogeography, explain the species-area relationship as t

124 nstruct, for the first time, a phylogeny and biogeography for the Trichinella complex, and show that

125 ogy in a unique position to move trait-based biogeography forward.

126 A temporally deeper historical biogeography framework may be required to address episod

127 k will aid studies of molecular systematics, biogeography, genetic differentiation, and conservation

128 obal ecosystem model determine phytoplankton biogeography, growth strategies and macromolecular compo

129 recurrent gene flow among lineages and where biogeography, habitat differentiation and mating systems

130 , the past influence of speciation on island biogeography has been obscured, and the species-area rel

131 Island biogeography has traditionally focused primarily on abio

132 New studies on phage biogeography have found that some phages are globally di

133 However, previous studies of C3 and C4 grass biogeography have often inadvertently compared species i

134 asis for the theoretical structure of island biogeography, have received little direct study.

135 owever, this is a challenge for the field of biogeography historically grounded on the species concep

136 anding the early diversification, historical biogeography, host-plant evolution, and fossil record of

137 processes or time lags at the warm edge; the biogeography hypothesis or extinction debt hypothesis),

138 We explored patterns of world-wide biogeography in a species-rich herbaceous group, the pap

139 etagenomics could be used to study microbial biogeography in complex habitats.

140 ole of phylogenetic knowledge and historical biogeography in explanations of global biodiversity patt

141 value for herbivores determine foliar sodium biogeography in herbaceous-dominated systems.

142 amined, despite the manifest significance of biogeography in other microbial systems.

143 our understanding of microbial micron-scale biogeography in samples from humans.

144 We evaluated Streptomyces biogeography in soils along a 1200 km latitudinal transe

145 Based on the results, bacterial biogeography in the Arctic seafloor sediments may be inf

146 tudies have considered predictions of island biogeography in the case of continental islands, where i

147 field of disease ecology and applications of biogeography in the epidemiology of infectious diseases.

148 However, there are few studies on functional biogeography in the marine environment, and none in the

149 ovide insights into population structure and biogeography in the mouth and form specific hypotheses a

150 ortant driver of different aspects of fungal biogeography, including the global distribution of commo

151 Moreover, anole biogeography increasingly reflects anthropogenic rather

152 s, and highlights the power of incorporating biogeography into understanding large-scale variability

153 product search and discovery strategies, and biogeography is a hot topic for microbial ecologists.

154 Countryside biogeography is an alternative framework, which recogniz

155 Our results suggest that microbial biogeography is controlled primarily by edaphic variable

156 oposed for the present time interval--island biogeography is dominated by the economic isolation of h

157 Historical biogeography is dominated by vicariance methods that sea

158 A theory of countryside biogeography is essential to conservation strategy in th

159 Island biogeography is fundamental to understanding colonizatio

160 drothermal vents globally indicate that vent biogeography is more complex than previously recognised.

161 The theory of island biogeography is most often studied in the context of oce

162 lation genetic processes and their effect on biogeography is needed to support elimination goals.

163 the dominant pattern of Southern Hemisphere biogeography is post-Gondwanan clade origins and subsequ

164 evolution theory developed in the context of biogeography is relevant to clinical microbiology and co

165 The equilibrium theory of island biogeography is the basis for estimating extinction rate

166 llenge in community ecology and evolutionary biogeography is to reveal the mechanisms underlying thes

167 When combined with biogeography, it can provide unique information about th

168 composition, yet our understanding of fungal biogeography lags far behind that of plants, animals and

169 ues for a more integrative use of islands in biogeography, macroecology, and conservation.

170 Functional biogeography may bridge a gap between field-based biodiv

171 ribe marine microbial communities, including biogeography, metabolic potential and diversity, mechani

172 erent hosts, we found that the rat microbial biogeography might represent a new reference, distinct f

173 We propose an island biogeography model of the microbial communities inhabiti

174 Wine grapes present a unique biogeography model, wherein microbial biodiversity patte

175 provide the simple link between climate and biogeography needed to predict the consequences of clima

176 A phylogenetic study of biogeography, niche evolution and diversification patter

177 eatures identified as important to amphibian biogeography, notably mountain ranges, large rivers such

178 variables and differs fundamentally from the biogeography of "macro" organisms.

179 new scheme to determine the distribution and biogeography of 294 samples of P. larvae from across six

180 ic understanding of the global diversity and biogeography of activated sludge bacterial communities w

181 e History Theory evolutionarily explains the biogeography of aggression and violence as strategic ada

182 We suggest that the biogeography of AM fungi is driven by unexpectedly effic

183 niche modeling to investigate the historical biogeography of an important ecological engineer: the du

184 The first quantitative reconstruction of the biogeography of Asian forest scorpions (Scorpionidae Lat

185 Mapping the biogeography of bacteria can shed light on interactions

186 Elucidating the biogeography of bacterial communities on the human body

187 g a DNA sequencing approach, we explored the biogeography of biofilm bacterial communities in 204 str

188 her, these results indicate that the altered biogeography of biofilm-grown cells and their enhanced p

189 and mineralogical factors contributed to the biogeography of both the abundant and the rare OTUs.

190 ovide evidence of large-scale changes in the biogeography of calanoid copepod crustaceans in the east

191 ngs contribute to a global assessment of the biogeography of chemosynthetic faunas and indicate that

192 These maps integrate the biogeography of coastal and deep-sea, pelagic and benthi

193 Here, we study the historical biogeography of Cycnoches to better understand the impac

194 To resolve the phylogeny and biogeography of Cylindraspis, we analysed a data set of

195 The biogeography of diel time partitioning is, however, poor

196 temperature-dependent hypoxia thus links the biogeography of diverse marine species to fundamental en

197 he origin of tarsier specializations and the biogeography of early tarsioid radiations.

198 genetic potential, community structure, and biogeography of environmental viruses.

199 as provided insights into the complexity and biogeography of human skin microbes.

200 and may contribute to altered immunity, the biogeography of immune-microbiome correlations among HEU

201 The importance of dispersal in the biogeography of Inga and other tree genera in Amazonian

202 obtained insight into the genome content and biogeography of many bacterial lineages inhabiting the s

203 population dynamics, genetic structure, and biogeography of many coastal species.

204 a unique opportunity to test factors shaping biogeography of marine microbial communities because the

205 Nevertheless, the biogeography of marine viruses has been slower to emerge

206 Mapping the complex biogeography of microbial communities in situ with high

207 The size, species composition, and biogeography of microbial communities is shaped by host

208 we present a framework for investigating the biogeography of microbial function by analyzing the dist

209 To address this gap, we characterized the biogeography of microbial N traits, defined as eight N-c

210 abundance of genomic-level information, the biogeography of microbiomes is almost entirely uncharted

211 vironmental function, population biology and biogeography of microorganisms cannot be rigorously expl

212 The global biogeography of microorganisms remains largely unknown,

213 how global warming may radically modify the biogeography of migratory species, and provides a genera

214 This study broadens the biogeography of N(2) fixation, highlights the interplay

215 However, the Holarctic biogeography of parthenogens has been hampered by very l

216 The biogeography of phages has only recently been investigat

217 al-scale community assembly and global-scale biogeography of plant symbiotic arbuscular mycorrhizal (

218 hs (GSSCP) have been used to reconstruct the biogeography of Poaceae, untangle crop domestication his

219 ecies has implications for understanding the biogeography of Prochlorococcus and its role in the ocea

220 of monsoon variations with the evolution and biogeography of rhizomyines.

221 As part of a broad-scale study of the biogeography of rocky reefs in the Gulf of California, M

222 Here, we clarify the taxonomy and biogeography of Russian Unionidae species based on the m

223 g spatially explicit genomic-scale data: the biogeography of speciation, lineage divergence and speci

224 The biogeography of Streptomyces was examined at regional sp

225 c processes have influenced the contemporary biogeography of Streptomyces.

226 features of CBMs which may contribute to the biogeography of symbiotic bacteria in the gut.

227 impact of climate warming on the functional biogeography of the Barents Sea, which is characterized

228 We conclude that the modern biogeography of the Cupressaceae conifers was shaped in

229 discussed in the context of the evolutionary biogeography of the Cupressaceae.

230 ibutes to unveil the complex Late-Quaternary biogeography of the ecotone belt occupied by marcescent

231 f point for future studies on the historical biogeography of the family.

232 an expansion of our current knowledge on the biogeography of the fungal community from deep-sea sedim

233 gal communities was mainly influenced by the biogeography of the host species.

234 verse GI locations enables mapping microbial biogeography of the mammalian GI tract and more accurate

235 To assess the biogeography of the nasal microbiota, we sampled healthy

236 Unlike the island biogeography of the past that was determined by geograph

237 tal vanadium had a significant effect on the biogeography of the rare biosphere.

238 also develop hypotheses about the historical biogeography of the Southern Hemisphere group Muehlenbec

239 We aimed at disentangling the historical biogeography of the subcosmopolitan liverwort genus Leje

240 al subgroups does not appear to be linked to biogeography of the viral isolates.

241 from these, however, and the true extent and biogeography of this are still not clear.

242 gerprints of Espeletia lineages followed the biogeography of this genus, suggesting that our untarget

243 verlooked functional lifestyle to expand the biogeography of this prominent marine genus.

244 nce of hibernation energetics constrains the biogeography of this species.

245 The functional biogeography of tropical forests is expressed in foliar

246 Together, these results suggest the biogeography of V. fischeri populations within the squid

247 of pressure on hydrothermal venting, and the biogeography of vent fauna.

248 rom the Earth's crust and mantle and for the biogeography of vent-endemic organisms.

249 GPS's accuracy and power to infer the biogeography of worldwide individuals down to their coun

250 olutionary history, dietary preferences, and biogeography, offering an unparalleled opportunity to di

251 r, little is known about their diversity and biogeography on a large spatial scale.

252 determine species occurrences, compared with biogeography or environmental conditions, remains largel

253 ogy, such as those that elucidate historical biogeography or uncover patterns of coevolution and dive

254 ry little is known about phage biodiversity, biogeography, or phylogeny.

255 Based on biogeography, our current understanding is that the Cari

256 lications to growth rates, foraging ecology, biogeography, plant metabolism, burn patients and sports

257 ome abundant and rare taxa presented similar biogeography, pointing to spatiotemporal structure in th

258 tern Brazil, to determine how classic island biogeography predictions and past vicariance explain the

259 e unified neutral theory of biodiversity and biogeography provides a dynamic null hypothesis for the

260 Functional biogeography provides a framework to address how ecosyst

261 Their biogeography provides essential clues to their cryptic r

262 logenetic analyses demonstrate that symbiont biogeography, rather than host taxonomy, is the main det

263 ture of the links between climate and animal biogeography remain largely obscure.

264 , global patterns and drivers of buzzing bee biogeography remain unexplored.

265 mixing of marine Bacteria restructures their biogeography remains to be tested.

266 Their phylogeny and historical biogeography resulting in a distant intercontinental dis

267 om across the United Kingdom possess sex and biogeography-specific odours.

268 Here, we present a biogeography study involving 25 previously undescribed b

269 y prevalent, and, do microbes have different biogeography than macroorganisms?

270 These classes demark a more complex biogeography than the latitudinally banded schemes propo

271 rns and processes in evolution, ecology, and biogeography that are of fundamental importance across t

272 nchialine fauna currently exhibit a disjunct biogeography that cannot be completely explained by plat

273 potheses on the factors that shape bacterial biogeography that have been overlooked in the past.

274 icrobiology: an adapted island model of lung biogeography, the effect of environmental gradients on l

275 ted on both otolith geochemistry and species biogeography, the model allows the aerobic limits of spe

276 estions such as anopheline phylogenetics and biogeography, the nature of species boundaries, and the

277 In biogeography, the physical world (a spatial extension of

278 Despite its importance for biogeography, the specific role of mountain ranges as a

279 us on the newly emergent field of functional biogeography: the study of the geographic distribution o

280 or avoiding simplistic application of island biogeography theory in conservation decisions.

281 Island biogeography theory indicates that, where the average ti

282 Island biogeography theory posits that species richness increas

283 Island biogeography theory predicts that the contribution of th

284 the main elements of niche theory and island biogeography theory suggests that environmental heteroge

285 pected biodiversity patterns based on island biogeography theory.

286 st how this evolutionary history fits island biogeography theory.

287 be considered in future studies of microbial biogeography to aid in our understanding of the diversit

288 emography and environment using experimental biogeography to forecast invasive and native species' po

289 ounted for in climate models, interacts with biogeography to influence plant ranges in a changing cli

290 historical factors, adaptive radiation, and biogeography, to provide a more detailed evolutionary ba

291 major land masses drifted apart, dinosaurian biogeography was molded more by regional extinction and

292 herefore, to progress with global functional biogeography, we should seek to understand the link betw

293 tions is founded on the principles of island biogeography, wherein the probability of species occurre

294 iversity plays an important role in symbiont biogeography, which may ultimately lead to a mosaic of f

295 ivers of terrestrial microbial diversity and biogeography, which presents a substantial barrier to un

296 idered as simply the amalgamation of classic biogeography with genetics and genomics; however, they d

297 ing factors include, among others, shifts in biogeography, with EPP spread facilitated by the global

298 When we visualize microbial biogeography within the colon, B. fragilis penetrates th

299 ironmental factors, including individuality, biogeography, xenobiotics, and disease.

300 Climate and physiology shape biogeography, yet the range limits of species can rarely