ライフサイエンスコーパス: biogeographic

1 es, including increases in herbs of northern biogeographic affinity and in forest canopy cover.

2 lower relative cover by species of northern biogeographic affinity, and greater compositional resemb

3 Druze biogeographic affinity, migration patterns, time of emer

4 Phylogenetic biogeographic analyses indicate a fundamental shift in s

5 Biogeographic analyses indicate that Gnaphalieae origina

6 orporating life history and growth form into biogeographic analyses reduced or eliminated the importa

7 Preliminary biogeographic analyses suggest larger range sizes in bio

8 Phylogenetic and biogeographic analyses support a South American origin o

9 ttern and process are inextricably linked in biogeographic analyses, though we can observe pattern, w

10 Phylogenetic biogeographic analysis further indicates that the Richmo

11 that omits the founder event parameter from biogeographic analysis is less suitable than the equival

12 Here, we present the first global biogeographic analysis of plant mating systems based on

13 regions; on 2n = 160 chromosomes of diverse biogeographic ancestries) identified 16 variants, of whi

14 of some CVD risk factors have suggested that biogeographic ancestry (BGA) may be a better predictor o

15 nucleotide polymorphisms (SNPs) can identify biogeographic ancestry (BGA); however, population substr

16 to support high plant production rates, but biogeographic and climate patterns further influenced th

17 ascinated by the prevalence of nestedness in biogeographic and community data, where it is thought to

18 tegration of cladistic analyses in a broader biogeographic and evolutionary context deserves increase

19 oils, and leaf habit data to reconstruct the biogeographic and evolutionary history of the American o

20 ut how plastic capacity may be influenced by biogeographic and evolutionary processes.

21 ies using Opiliones as test cases to address biogeographic and evolutionary questions more broadly.

22 strained phylogenetic framework coupled with biogeographic and evolutionary rate studies.

23 However, biogeographic and fossil evidence implies that the evolu

24 nsistent with its repeated evolution and its biogeographic and habitat distribution.

25 ange and may represent overlooked drivers of biogeographic and large-scale biodiversity patterns.

26 her, we show the importance of incorporating biogeographic and phylogenetic history in predicting com

27 Against a backdrop of no biogeographic and phylogenetic patterning in population

28 aScript to generate in-browser animations of biogeographic and phylogeographic histories from annotat

29 In this study, we present phylogenetic, biogeographic, and functional analyses of a previously u

30 span a range of temperatures within a single biogeographic area, allow us to take the laboratory into

31 ast Java and Bali are recognized as distinct biogeographic areas.

32 mus of Kra represents a significant southern biogeographic barrier between freshwater mussel faunas o

33 across the Carpentarian Barrier, a prominent biogeographic barrier dividing faunas spanning the monso

34 day San Francisco-Bay Delta region; a common biogeographic barrier for the flora and fauna of Califor

35 ons, current and historical environment, and biogeographic barriers determine community structure is

36 diversity across environmental gradients and biogeographic barriers provides insight into the potenti

37 cast species responses to climatic change or biogeographic barriers while gaining unique insights abo

38 homogenization of species composition across biogeographic barriers(1-3).

39 ged along environmental gradients and across biogeographic barriers.

40 r, the success of species transported across biogeographic boundaries suggests a stronger role for ev

41 extratropical regions), but particularly at biogeographic boundaries where steep richness gradients

42 fts in genotype frequencies often align with biogeographic boundaries, providing intraspecific concor

43 rnia south of Point Conception, a recognized biogeographic boundary, whereas further north, W. subtor

44 ic division coincides with a trans-Nullarbor biogeographic boundary.

45 The biogeographic changes were further linked to large-scale

46 common garden to study the phylogenetic and biogeographic/climatic controls on g(sn) and further ass

47 of diversity, there remain few standardized biogeographic comparisons of community effects of specie

48 We show that species introductions reduce biogeographic compartmentalization of the global meta-ne

49 brid-Lambda makes it possible to investigate biogeographic concordance among high fecundity species e

50 ated PNV evapotranspiration adapted to local biogeographic conditions, on global dry lands, where soi

51 hese lineages, the winter ranges served as a biogeographic conduit for temperate-to-tropical coloniza

52 postulating the existence at that time of a biogeographic connection between northern South America

53 tural environments, a broad phylogenetic and biogeographic context could provide insights into potent

54 s and multiscale approaches that include the biogeographic context of species traits.

55 ability to separate the effects of these two biogeographic controls is limited by the enormous enviro

56 This biogeographic convergence is particularly striking becau

57 they are considered to have driven increased biogeographic cosmopolitanism, but quantitative tests of

58 Using biogeographic data from across vascular plants, we teste

59 e, we integrate physiological, climatic, and biogeographic data to calibrate and then map a key metab

60 Here, we combine biogeographic data with the fossil record to investigate

61 Using biogeographic databases of the global distributions of m

62 ave the propensity to facilitate episodes of biogeographic differentiation and influence patterns of

63 f a novel morphological trait, an episode of biogeographic dispersal, or the onset of an ecological a

64 ecosystems, but little is known about their biogeographic distribution and community structure in te

65 genome annotation, taxonomic classification, biogeographic distribution and in silico host prediction

66 These data are used to create chemical biogeographic distribution maps for biomedically valuabl

67 t these sphenodontians achieved a widespread biogeographic distribution much earlier than previously

68 This study aimed to understand how the biogeographic distribution of a crucial endemic copepod

69 Across the planet the biogeographic distribution of human cultural diversity t

70 In this paper we focus on the biogeographic distribution of mammal species and human c

71 By mapping our results onto the biogeographic distribution of the dominance-tolerance tr

72 measure of their true genetic diversity and biogeographic distribution.

73 situ populations (most 'abundant') and have biogeographic distributions distinct from previously ava

74 archaeological evidence, reveals a pre-human biogeographic divergence, and an unexpected human role i

75 o reconstruct spatial patterns of freshwater biogeographic divides throughout Asia.

76 Here, we present an updated freshwater biogeographic division of mainland Southeast Asia and de

77 The results showed strong biogeographic endemism pattern in soil bacteria were exi

78 a by Homo erectus was not only a significant biogeographic event but also a major evolutionary thresh

79 s concerning the impact of morphological and biogeographic events on rates of diversification in Adox

80 and the B subgenome of cultivated peanut and biogeographic evidence, we conclude that A. ipaensis may

81 The biogeographic expansion of modern humans out of Africa b

82 power to separate the effects of historical biogeographic factors (e.g., island age) from the effect

83 climate change will be highly influenced by biogeographic factors, emphasizing the value of integrat

84 on and extinction, a species' ecological and biogeographic footprint-its occupancy-will vary in respo

85 ve occurrence models typically used for such biogeographic forecasts-suggest the urgency of incorpora

86 ate and land use highlights the need for new biogeographic frameworks to understand evolutionary chan

87 n in northeastern China, which fills a large biogeographic gap in Eurasia.

88 erve network spans a major environmental and biogeographic gradient, making it a challenge to assess

89 thropogenic drivers are layered atop natural biogeographic gradients.

90 nd ANPP differ between systems with distinct biogeographic histories and species assemblages.

91 is consistent across grasslands of disparate biogeographic histories and taxonomic representation.

92 e of local environments and evolutionary and biogeographic histories in generating these patterns.

93 ceae, and molecular patterns indicate shared biogeographic histories of Castanopsis, Castanea, Lithoc

94 tial influences of distinct phylogenetic and biogeographic histories on the isotopic niches occupied

95 esses that determine community assembly with biogeographic histories that span geological time scales

96 lar structure and physiognomy, yet disparate biogeographic histories.

97 logy and biophysics but struggles to capture biogeographic history and ecological dynamics that deter

98 , as a model system to evaluate the roles of biogeographic history and marginal population genetics i

99 n years ago have limited insights into their biogeographic history during the Cretaceous.

100 struct its evolutionary history, examine its biogeographic history in the archipelago, and to estimat

101 r) ranges and applied it to the inference of biogeographic history in the emberizoid passerine birds.

102 Specifically, we test if Cyrtognatha biogeographic history is consistent with an ancient vica

103 Biogeographic history is likely to have had a particular

104 otentially used as a model to understand the biogeographic history of additional plant groups in the

105 olution in the Sclerodermatineae follows the biogeographic history of disjunct plant communities asso

106 ly recent phenomenon, overprinting a complex biogeographic history of dramatic geographic range shift

107 vidence that eustatic changes influenced the biogeographic history of the AF.

108 d distribution must have been crucial in the biogeographic history of the Atlantic Forest, and forest

109 taceous, complicating reconstructions of the biogeographic history of the placental radiation.

110 t interactions, and we explore ways that the biogeographic history of their host plants may have affe

111 We model the biogeographic history of this group and the evolutionary

112 comprehensive analysis of the phylogeny and biogeographic history of Trichinella using the variation

113 s15) fragments to reconstruct the phylogeny, biogeographic history, and patterns of diversification o

114 on Pleistocene connectivity, suggesting that biogeographic history-a factor often overlooked in biodi

115 8 spatially explicit predictions of 12 major biogeographic hypotheses, we show that mixed models grea

116 t species expected to experience substantial biogeographic impacts from rising temperatures.

117 al model to test the relative ecological and biogeographic impacts of reproductive mode and ploidy be

118 Neustonic daphniids have more divergent biogeographic lineages than previously appreciated.

119 hat ECM spore banks correlated strongly with biogeographic location, but not with the identity of con

120 hift of microbial metabolites were driven by biogeographic location.

121 h predictions from the Expansion-Contraction biogeographic model, with a poleward post-glacial shift

122 five nuclear and plastid regions) and twelve biogeographic models, we infer that the most recent comm

123 s Lepilemur and to evaluate evolutionary and biogeographic models.

124 n discrete morphological traits, episodes of biogeographic movement, etc.) under both hypothesis-test

125 We evaluated methods of controlling for biogeographic or environmental variation across networks

126 p explain patterns and processes shaping the biogeographic organisation of species.

127 by providing insight on the phylogenetic and biogeographic origin of Perissodactyla.

128 ever the functional significance of species' biogeographic origin remains highly contentious.

129 ortantly, explicit consideration of resident biogeographic origin.

130 over 150 years of study in these areas, the biogeographic origins of these rich communities of land-

131 responsible for a large part of the observed biogeographic pattern of increasing annual invasion in U

132 eds, particularly in wet tropical forests, a biogeographic pattern that is not well accounted for in

133 fy the underlying mechanisms generating this biogeographic pattern.

134 enerating and maintaining the soil bacterial biogeographic pattern.

135 decreased at all sites mirroring the natural biogeographic pattern.

136 Here, we examine whether recent biogeographic patterns across California are consistent

137 ese findings may help to explain many of the biogeographic patterns and connections we currently see

138 kelp forest monitoring datasets to evaluate biogeographic patterns and rates of change of key functi

139 The models estimate global biogeographic patterns and seasonal variability of cell

140 ssil record and present the distribution and biogeographic patterns derived from over 16,000 records

141 factors that may help explain the decoupled biogeographic patterns for the two genes.

142 hat larval tolerance can explain large-scale biogeographic patterns for this species across its range

143 ced species on ecological networks and their biogeographic patterns globally.

144 Biogeographic patterns have been demonstrated for a wide

145 review is that distinctive phylogenetic and biogeographic patterns in clades endemic to different ma

146 The long-term analysis suggests that broad biogeographic patterns in deep-sea macrofauna community

147 Our results suggest that biogeographic patterns in mating system are more likely

148 Our data highlighted biogeographic patterns in microbial community compositio

149 The study demonstrates strong global biogeographic patterns in richness and community composi

150 gher latitudes and among some biomes, but no biogeographic patterns in the frequency of self-incompat

151 which body temperatures translate into major biogeographic patterns is of paramount importance.

152 y, our findings suggest that bacteria follow biogeographic patterns more typical of macroscopic organ

153 rth American primates corresponds to similar biogeographic patterns noted among fossil plants.

154 rehensive evaluation of the phylogenetic and biogeographic patterns of antiinfective compounds from s

155 les, non-competitive factors may have driven biogeographic patterns of brachiopods and bivalves.

156 s, Plasmodium and Haemoproteus, and analysed biogeographic patterns of lineages across islands and av

157 Here we investigate biogeographic patterns of marine cyanophages that infect

158 is potentially a means to reconcile complex biogeographic patterns of Symbiodinium phylogenetic dive

159 Here, we determined the biogeographic patterns of the functional dissimilatory s

160 Here, we document basic biogeographic patterns of time partitioning by mammals a

161 Here we compared biogeographic patterns of two Palaearctic shorebirds wit

162 but the determinants of fungal diversity and biogeographic patterns remain poorly understood.

163 subcritical thermal events can contribute to biogeographic patterns via physiological differences tha

164 usters, populations, and morphology revealed biogeographic patterns whereby viral communities were pa

165 tions show the production and maintenance of biogeographic patterns, characterized by distinct provin

166 e some of the first data linking large-scale biogeographic patterns, community-scale interaction outc

167 eir isotopes as well as measured and modeled biogeographic patterns, have revolutionized our understa

168 Tcrit and Tmax followed similar biogeographic patterns, increasing linearly ( 8 degrees

169 diversity but also reshaping ecosystems and biogeographic patterns.

170 selection and neutral evolution in producing biogeographic patterns.

171 phages display striking seasonal and spatial biogeographic patterns.

172 anic C) played relatively small roles in the biogeographic patterns.

173 ransport limitation in determining microbial biogeographic patterns.

174 tionships, timing of diversification(s), and biogeographic patterns.

175 ciency, such as vessel diameter, should show biogeographic patterns; but critical tests of these pred

176 Leveraging a biogeographic perspective will provide insight into the

177 The island ecosystem conforms to island biogeographic predictions of bat species loss, in which

178 hy and environmental, biotic, and historical biogeographic predictors of avian social behavior.

179 intra-island speciation as the most frequent biogeographic process underlying diversification, contra

180 greatest biological invasions highlight how biogeographic processes and biotic interactions can shap

181 ggest that the morphological integration and biogeographic processes are the main drivers of their di

182 ions may be the most influential factor; and biogeographic processes are thought to be of greater imp

183 n opportunity to understand evolutionary and biogeographic processes at a global scale.

184 Exploring biogeographic processes at diverse geographic scales imp

185 n for providing insights into the historical/biogeographic processes driving population genetic struc

186 al tolerances of species to evolutionary and biogeographic processes, phylogenetic niche conservatism

187 This new fauna constitutes a new biogeographic province with North American affinities an

188 essional sequence for vent fauna in this new biogeographic province.

189 tarctic vent ecosystems represent a new vent biogeographic province.

190 The taxonomic identities used to define biogeographic provinces are routinely accompanied by dia

191 partitions in the sea against a backdrop of biogeographic provinces defined by taxonomy, endemism, a

192 ies have suggested the existence of separate biogeographic provinces in the Atlantic and the North We

193 rhaps by excretory physiology, into distinct biogeographic provinces tracking latitude, not geographi

194 tribution of these genera identifies coastal biogeographic provinces where fauna with high intrinsic

195 l species are distributed across two or more biogeographic provinces, shifts in genotype frequencies

196 ogeographic structure corresponding to major biogeographic provinces.

197 hallow subsurface nutrients between distinct biogeographic provinces.

198 In this paper we document the BPH biogeographic range expansion in China over the 20-year

199 , radiocarbon dates, fossil occurrences, and biogeographic range information among others.

200 d-Eocene diversification is aligned with the biogeographic range shift to Africa where many of the mo

201 o assess relationships among dispersal mode, biogeographic range size, and diversification rate.

202 senting 205 amphibian species across a broad biogeographic range.

203 that sensitivity to toxicants differs across biogeographic ranges, shallow-water species may be suita

204 for dispersal ability), migratory habit, and biogeographic realm across 126 vespertilionid bat specie

205 and the strength of this effect depended on biogeographic realm and vegetation type.

206 community phylogenetic diversity, latitude, biogeographic realm and vegetation type.

207 divergences occurred largely within a single biogeographic realm during the Paleogene, with a few lon

208 rctic marine benthos may constitute the last biogeographic realm where barriers (oceanographic curren

209 controlling for the effects of migration and biogeographic realm.

210 ed on the divergent histories of the world's biogeographic realms and their native biotas.

211 the degree of phylogenetic clustering among biogeographic realms are related to differential losses

212 Biogeographic realms differ significantly and importantl

213 Marine biogeographic realms have been inferred from small group

214 Our biogeographic reconstruction shows that Pteronymia origi

215 Although biogeographic reconstructions cannot refute a vicariant

216 rth's lower latitudes, leading to historical biogeographic reconstructions favoring a Gondwanan origi

217 time calibrations, and geologically informed biogeographic reconstructions to provide a well-supporte

218 es new constraints on models of Afrotropical biogeographic refugia and early modern human population

219 regions are discussed; generic diversity by biogeographic region is presented in tabular form.

220 xonomic accumulation graphs are presented by biogeographic region, indicating an ongoing need for tax

221 esentativeness (r >/= 0.8) was influenced by biogeographic region, sampling method, sampling effort o

222 and explaining diversity gradients within a biogeographic region.

223 formed at the community level across a large biogeographic region.

224 tion in the countries of the European boreal biogeographic region.

225 species occurrences among sites across this biogeographic region.

226 The formation and maintenance of biogeographic regions and the latitudinal gradient of sp

227 tterns and relative generic diversity across biogeographic regions are discussed; generic diversity b

228 or shaping richness gradients and delimiting biogeographic regions has not been well established.

229 lusters using 32 viral metagenomes from four biogeographic regions in the Pacific Ocean that vary by

230 erogeneous distribution of species ranges in biogeographic regions should concentrate interactions in

231 tential negative impacts and the most likely biogeographic regions to be affected by these potential

232 ontinuity are located towards the centres of biogeographic regions where species turnover tends to be

233 Conserving biogeographic regions with especially high biodiversity,

234 gene transfer between cohabitants of similar biogeographic regions, acquisition of nitrogen-fixing ca

235 often have shared species richness patterns, biogeographic regions, biomes and biodiversity hotspots.

236 vely insensitive to abiotic variation across biogeographic regions, offer great potential for develop

237 olutionary lineages, distributed in distinct biogeographic regions-north-western Africa, eastern Afri

238 s across resource gradients within and among biogeographic regions.

239 estrial ecosystems are dominated by distinct biogeographic regions.

240 ral species between the Oriental and African biogeographic regions.

241 by species' origins in climatically distinct biogeographic regions.

242 eustonic daphniids that were associated with biogeographic regions.

243 Here, we studied the phylogenetic and biogeographic relationships amongst the species of this

244 These results quantify the composition and biogeographic relationships between gut microbial commun

245 however blur intra-species relationships and biogeographic resolution.

246 The biogeographic response of oceanic planktonic communities

247 e beyond a warming fingerprint in studies of biogeographic responses by considering a more multifacet

248 Studies of observed biogeographic responses to 20th century climate change h

249 Understanding recent biogeographic responses to climate change is fundamental

250 Predicting ecological and biogeographic responses to these changes constitutes an

251 0th century and review empirical evidence of biogeographic responses to these changes, particularly e

252 e changes interact with temperature to drive biogeographic responses.

253 variation in freshwater fishes at global and biogeographic scales and determine how these drivers aff

254 ing range limits and preventing invasions at biogeographic scales is more controversial, partly becau

255 understanding of drought impacts at stand-to-biogeographic scales, including management options, and

256 ecimens of 27 species, we recovered a robust biogeographic scenario that shows the Indo-West Pacific

257 accepted or rejected this identification and biogeographic scenario.

258 eontological datasets to disentangle complex biogeographic scenarios and reveal unexpected biodiversi

259 rial genomes to reconstruct phylogenetic and biogeographic scenarios with fossil-based calibrations.

260 w-marine benthic faunas, defined by existing biogeographic schemes, can be predicted with 89-100% acc

261 This clear biogeographic signal suggests that infectious disease as

262 llowing for high-fidelity comparisons across biogeographic sites.

263 Despite great differences in biogeographic, social, and economic aspects of our study

264 We extend previous results of biogeographic stratification, identifying a new subspeci

265 hat habitat continuity is a top predictor of biogeographic structure and the richness gradient of eas

266 Although the clear global biogeographic structure in avian social behavior carries

267 s of how environmental factors influence the biogeographic structure of biotas are essential for unde

268 e left a permanent mark on the taxonomic and biogeographic structure of the modern biota, despite the

269 e sufficient to model the response of marine biogeographic structure to past and future changes in cl

270 geographical barriers to gene flow producing biogeographic structure.

271 MHC diversity in populations with different biogeographic structure.

272 tative methods to analyze four components of biogeographic structure: connectedness, clustering, rang

273 ver, the coarse-scale data typically used in biogeographic studies have limited inferential power to

274 ly, we perform a global meta-analysis of bat biogeographic studies, spanning more than 700 species.

275 , Cabo Verde should be given the status of a biogeographic subprovince within the West African Transi

276 the Western Indochina represents a separate biogeographic subregion having a largely endemic freshwa

277 g rainforest expansion and contraction in 21 biogeographic subregions in northeast Australia across f

278 Here, we have coupled a chemical-biogeographic survey of chromopyrrolic acid synthase (CP

279 HhMAN1 was found to be widespread in a broad biogeographic survey of H. hampei accessions, indicating

280 Here we directly test these biogeographic theories by comparing a Neotropical countr

281 eralizes our findings, showing that separate biogeographic theories for countryside and island ecosys

282 marine islands has led to advances in island biogeographic theory accommodating both evolutionary and

283 ands have been crucial to the development of biogeographic theory, yet little is known about correspo

284 fy overarching physiological, behavioral, or biogeographic traits determining species' responses to c

285 This region represents an important biogeographic transition zone that lies <150 km north of

286 communities in northern California and other biogeographic transition zones.

287 These findings clarify biogeographic trends and the underlying basis of drought

288 ance, potentially contributing to well-known biogeographic trends in leaf size.

289 high spatial resolution to determine whether biogeographic trends occurred at the centimeter scale.

290 apacity, and more-fundamental ecological and biogeographic understanding, will come from integration

291 e coherency and validity of Macaronesia as a biogeographic unit using six marine groups with very dif

292 concept of Macaronesia as a coherent marine biogeographic unit.

293 teract with environmental gradients to cause biogeographic variability in the net strength of trophic

294 sequences exhibited significant genomic and biogeographic variability, highlighting challenges in th

295 This biogeographic variation in nutrient effects on plant-her

296 Our results highlight that climate-related biogeographic variation in soil C responses to temperatu

297 annual precipitation primarily explained the biogeographic variation in the decomposition rate and te

298 A framework for incorporating biogeographic variation into reserve network assessments

299 The biogeographic variation of life has predominantly been s

300 ic CO(2) concentrations): maximum tree size, biogeographic water-deficit affiliation and wood density