ライフサイエンスコーパス: biogeographical

1 While biogeographical algorithms using next-generation sequenc

2 e-calibrated mtDNA phylogeny, for subsequent biogeographical analyses in BioGeoBEARS of over 100 orig

3 congruent with the geological literature and biogeographical analyses of other taxa from South and So

4 Biogeographical analyses suggest that Evacanthinae origi

5 Biogeographical analyses suggest that local mainstem ele

6 y generated, we employed molecular clock and biogeographical analyses to infer the evolutionary histo

7 The biogeographical analysis localised proto-Druze to the mo

8 We performed a 3D biogeographical analysis of the microbiota of mouse ceca

9 c structure, and are a valuable new tool for biogeographical analysis.

10 Biogeographical and diversification analyses show the Mi

11 Understanding the biogeographical and diversification processes explaining

12 sting diversity pattern, we investigated the biogeographical and ecological origin of this subfamily,

13 great importance; however, knowledge of the biogeographical and ecological relationships between phy

14 Biogeographical and ecological theory suggests that spec

15 This study reveals new insights into biogeographical and ethnic effects upon the pregnancy an

16 Here, we uncover the global biogeographical and evolutionary patterns of Asteraceae

17 expansion persists, providing insights into biogeographical and evolutionary processes underlying gl

18 of biochemical, immunological, behavioural, biogeographical and fossil evidence relating to the evol

19 ant biochemical, immunological, behavioural, biogeographical and fossil evidence to elucidate the evo

20 evolution with animal pollination over large biogeographical and macroevolutionary scales.

21 rk of the Orchidaceae that paves the way for biogeographical and macroevolutionary studies.

22 rs, principally precipitation regimes, shape biogeographical and phenological patterns in tropical re

23 Insight on the biogeographical and phenotypic variations of Cacospongia

24 Integrating both biogeographical and phylogenetic perspectives, our study

25 We find a clear need for more ecological, biogeographical, and evolutionary studies on the impact

26 age based on paleobotanical, climatological, biogeographical, and geological data, and a tentative es

27 encrypted antibiotic peptides from the same biogeographical area display synergistic antimicrobial a

28 ies, which are ecotones between two distinct biogeographical areas, interactions are better predicted

29 d variant calling, including group size, the biogeographical backgrounds of the individuals who have

30 y served as a stepping-stone to overcome the biogeographical barrier represented by the Amazon-Orinoc

31 these results suggest a strong and long-term biogeographical barrier to gene flow.

32 of the Anthropocene epoch is the erosion of biogeographical barriers by human-mediated dispersal of

33 Saharo-Arabian Desert is one of the largest biogeographical barriers on Earth, impeding dispersals b

34 ating biodiversity or potentially delimiting biogeographical boundaries at regional scales in the aby

35 olonization was not inhibited by traditional biogeographical boundaries such as Wallace's Line.

36 pots and the other on species from permeable biogeographical boundaries.

37 connections to the leaf economics spectrum, biogeographical characteristics, evolutionary biology an

38 eal and Boreal-Tundra species, (ii) assessed biogeographical, climatic and local borealisation driver

39 amily, such as Ceratopetalum, have indicated biogeographical connections between South America and Au

40 nclear, as are the rate of evolution and the biogeographical consequences of giant seeds.

41 To illustrate the biogeographical consequences of such drastic migratory s

42 se two sets of data or to consider them in a biogeographical context.

43 bial interactions in both spatiotemporal and biogeographical contexts while also considering person-,

44 feedbacks for an invasive tree across broad biogeographical contexts.

45 butions ('climatic equilibrium'), when other biogeographical controls are often reliably established.

46 ships to both pathogen spillover and general biogeographical correlations between diversity and disea

47 ronmental coverage data provides informative biogeographical data for poorly known tropical landscape

48 synthetic analysis of molecular, fossil and biogeographical data gives a remarkably consistent scena

49 y provide significant palaeoevolutionary and biogeographical data regarding the evolution of life on

50 To resolve the ratite phylogeny and provide biogeographical data to examine these issues, we have he

51 research combining genetic, ecological, and biogeographical data to fully understand Rhodniini speci

52 aphorism is largely challenged by microbial biogeographical data, even weak versions of the claim le

53 getic constraints; phylogenetic constraints; biogeographical determinants; habitat structure; and com

54 between allele frequencies and behavioral or biogeographical differences between species, casting dou

55 about the mechanisms underlying the observed biogeographical differences in cell size composition of

56 Although biogeographical differences in community assembly mechan

57 We suggest that biogeographical differences in the relative importance o

58 EICA-like trade-offs, we do not know if the biogeographical differences we found were caused by trad

59 acks, large red deer tracks and steppe bison biogeographical distribution in Iberia.

60 ula: see text](50) and HSM(50) influence the biogeographical distribution of Amazon tree species.

61 ucture explains significant variation in the biogeographical distribution of bacteria at continental

62 In this review, we focus on the biogeographical distribution of genetic variation and ad

63 ities exhibit similar colonization dynamics, biogeographical distribution, and responses to dietary p

64 ulator of colonic microbiota composition and biogeographical distribution, is a critical orchestrator

65 into species groups associated with distinct biogeographical distributions and diversification histor

66 dicate that small soil animals have distinct biogeographical distributions and provide unique evidenc

67 a powerful way to conceptualize and analyze biogeographical distributions in relation to spatial env

68 Biogeographical distributions were employed to generate

69 recent hypothesis claims that microbes lack biogeographical divergence because their population size

70 The present study investigates the biogeographical diversification of the New World buthid

71 Here we present genetic, morphological and biogeographical evidence suggesting that these riverine

72 mer hypothesis gains additional support from biogeographical evidence, but both scenarios are current

73 l issues of developmental, morphological and biogeographical evolution.

74 functional diversity was triggered by their biogeographical expansion beyond Africa.

75 or are an oversimplification of the complex biogeographical forces that determine species spatial ab

76 lobal change on ecosystem functioning across biogeographical gradients can benefit from enhanced capa

77 elated plant physiological stoichiometry and biogeographical gradients in soil substrate age and then

78 Model simulations provide insight into the biogeographical heterogeneity among lumen, mucus, and fe

79 nents, despite highly divergent land use and biogeographical histories in these regions.

80 ee species to infer the divergence dates and biogeographical histories of these species and the effec

81 netic signature associated with the species' biogeographical history across the Mediterranean region.

82 phylogeny using 12 genes, to investigate the biogeographical history and diversification dynamics in

83 address this knowledge gap by inferring the biogeographical history and diversification dynamics of

84 North America, indicating a more complicated biogeographical history for this important Gondwanan fam

85 Here, we provide insights into the biogeographical history of Antarctic freshwater diatoms,

86 Here, we reveal the biogeographical history of hyperdiverse and flightless T

87 ps, hybridization and introgression, and the biogeographical history of primate groups.

88 ocesses and complicates understanding of the biogeographical history of species.

89 We aim to infer the evolutionary and biogeographical history of the honey bee from mitochondr

90 The biogeographical history of the north-south divergence ev

91 se scorpions, providing a timeline for their biogeographical history that can be summarized into four

92 lifornian golden cup oaks with an intriguing biogeographical history.

93 onary units and infer their evolutionary and biogeographical history.

94 rrence in the Northern Hemisphere challenges biogeographical hypotheses of a Gondwanan origin of crow

95 lationships and associated morphological and biogeographical hypotheses.

96 biota and can be used to evaluate competing biogeographical hypotheses.

97 not supported by molecular data, the general biogeographical hypothesis is supported.

98 ral shared derived features; this supports a biogeographical hypothesis that Madagascar and South Ame

99 Understanding these historical and biogeographical influences is essential for the effectiv

100 ty(14) that conceal important ecological and biogeographical insights.

101 Mya in Gondwana, well before the thermal and biogeographical isolation of Antarctica.

102 barrier height, type and density, as well as biogeographical location.

103 es and might help resolve the ecological and biogeographical mechanisms structuring biodiversity.

104 not been previously investigated with modern biogeographical methods.

105 of mitochondrial haplogroups corroborated by biogeographical modelling suggested that Southwest China

106 Time-calibrated phylogenies and biogeographical models suggest that these frogs colonize

107 ut each accesses this resource in a distinct biogeographical niche.

108 Classical biogeographical observations suggest that ecosystems are

109 a community-level perspective rather than a biogeographical one, focusing on terrestrial systems, an

110 tion structure were strongly associated with biogeographical origin.

111 iurnal fluctuations due to compositional and biogeographical oscillations in the microbiota.

112 Remote sensing of specific climatic and biogeographical parameters is an effective means of eval

113 on communities displayed a temporally stable biogeographical pattern among lakes, which was driven by

114 cal functions, yet little is known about its biogeographical patterns and community assembly processe

115 ntifying the mechanisms that shape microbial biogeographical patterns and how these patterns vary und

116 So far, relatively little is known about the biogeographical patterns and mechanisms structuring the

117 tly and build trait-based predictions of the biogeographical patterns exhibited by microbes.

118 o address this obstacle, we investigated (a) biogeographical patterns in attached and waterborne micr

119 Biogeographical patterns in diversity and species intera

120 ndamental ecological processes and microbial biogeographical patterns in paddy soils.

121 s of interacting plant species largely shape biogeographical patterns in plant-plant and plant-soil i

122 and evolution of species and shaping larger biogeographical patterns in space and time akin to eleva

123 hese findings improve our ability to predict biogeographical patterns of Antarctic terrestrial biodiv

124 t sequencing of the 16S rRNA gene to explore biogeographical patterns of bacteria across > 80 surface

125 siological phenomenon can affect large-scale biogeographical patterns of insects is largely unknown.

126 Here, we summarised biogeographical patterns of New World vertebrates and co

127 In contrast to biogeographical patterns of planktonic marine microbial

128 Results revealed similar biogeographical patterns of rare and abundant bacteria a

129 nderstanding of the evolutionary history and biogeographical patterns of Tetraopes.

130 c marker to investigate the biodiversity and biogeographical patterns of this important pest, in nati

131 zing relict prairie soils and found that the biogeographical patterns were largely driven by changes

132 tion as an overlooked driver of global plant biogeographical patterns with implications for contempor

133 Understanding the biogeographical patterns, and evolutionary and environme

134 our understanding of how protist diversity, biogeographical patterns, and members of the rare biosph

135 ing and substrate lability predominantly set biogeographical patterns, and we identified deep-ocean "

136 history limit plant distributions and affect biogeographical patterns, but how their relative importa

137 elucidation of global macro-evolutionary and biogeographical patterns, improving our ability to predi

138 s of tick-host and -habitat associations and biogeographical patterns, in the context of the newly de

139 ial lateral advection and preserves regional biogeographical patterns, indicating deposition by a sim

140 enic pressure and land use alter these plant biogeographical patterns.

141 ns are an excellent system for understanding biogeographical patterns.

142 in the tropical soil is possibly related to biogeographical patterns.

143 n of maritime connectivity has ranged from a biogeographical perspective that considers the sea as a

144 cies for studying invasion hypotheses from a biogeographical perspective.

145 Plant invasions are biogeographical phenomena that may involve shifts in bel

146 Biogeographical, physiological, and paleoecological evid

147 nnate immunity and the stool microbiome in a biogeographical population-specific way.

148 t heat tolerances vary mainly as a result of biogeographical processes and drift.

149 sularity and are thought to be shaped by the biogeographical processes and evolutionary histories of

150 s study underlines that both environment and biogeographical processes are responsible for driving ar

151 ogy has paradoxically led to neglecting real biogeographical processes in the study of macroevolution

152 We explored demographic and biogeographical processes that shaped the genetic divers

153 ith climate gradients reflecting large-scale biogeographical processes.

154 ey predictors of zoonotic reservoirs include biogeographical properties, such as range size, as well

155 We propose to redefine the Lusitanian biogeographical province, in which we include four ecore

156 ties on the kelp Ecklonia radiata from three biogeographical provinces spanning 10 degrees of latitud

157 iomass, with differing contributions in five biogeographical provinces spanning tropical to subpolar

158 t the scale of the whole earth and its major biogeographical provinces, those steady states respond l

159 three freshwater wetlands that span multiple biogeographical provinces.

160 pores, a crucial factor governing dispersal, biogeographical range, ecological function, and infectio

161 cords from 15 sites on 13 islands within the biogeographical realm of Oceania.

162 of frugivores on Annonaceae diversity across biogeographical realms suggest that biogeography modulat

163 across measures of phylogenetic relatedness, biogeographical realms, and highly invaded countries, ev

164 Israel's Mediterranean biogeographical region is characterized by high habitat

165 using a complete phylogeny (5,949 species), biogeographical regionalization and null-model compariso

166 Biogeographical regions (geographically distinct assembl

167 n patterns of Tetraopes species across major biogeographical regions and their colonization of the Am

168 ociation became obscured by variation across biogeographical regions at the scale of Amazonia, resemb

169 istic networks from five communities in four biogeographical regions of South America.

170 entify a general spatial organization within biogeographical regions of terrestrial and marine verteb

171 We detect seven types of areas in these biogeographical regions that reflect unique combinations

172 uted experiments in different ecosystems and biogeographical regions to assess the extent to which va

173 he genomes of 110 RNB from diverse hosts and biogeographical regions, and undertook a global explorat

174 Across crops, years and biogeographical regions, crop-visiting wild bee communit

175 from the core to the transition zones of the biogeographical regions, reflecting gradients in the bio

176 When compared to various world-wide biogeographical regions, the Arabian Peninsula exhibits

177 Springtails were collected from two biogeographical regions, the maritime and the continenta

178 er is central to understanding the nature of biogeographical regions.

179 Life on Earth is a mosaic distributed across biogeographical regions.

180 and extremely low divergence observed among biogeographical regions.

181 perience rapid climate-driven changes across biogeographical regions.

182 entification and delimitation of the world's biogeographical regions.

183 eving a larger number of commonly recognized biogeographical regions.

184 EICA predicts that biogeographical release from natural enemies initiates a

185 or phylogenetic groups, suggesting a general biogeographical rule for range size variation.

186 n these groups and were compared at multiple biogeographical scales to ascertain whether invasive thi

187 ee selection shapes MHC diversity in complex biogeographical scenarios where other evolutionary proce

188 processes govern MHC diversity in different biogeographical scenarios: positive selection occurs bro

189 hness among lineages of trees from all major biogeographical settings of the lowland wet tropics.

190 Biogeographical shifts are a ubiquitous global response

191 These biogeographical shifts are in agreement with recent chan

192 We demonstrate that strong biogeographical shifts in all copepod assemblages have o

193 onally complex because detecting concomitant biogeographical shifts in competitive ability and consum

194 Large-scale biogeographical shifts in vegetation are predicted in re

195 models forecasting species vulnerability and biogeographical shifts under future climate change.

196 Mexico's biogeographical situation places it at risk from invasiv

197 nts for variation in Rdark across this large biogeographical space.

198 Species relationships were resolved, and biogeographical stochastic mapping identified intra-isla

199 hips differed between forest types and among biogeographical strata.

200 positively associated to carbon stock in all biogeographical strata.

201 Here we reconstructed the biogeographical structure and evolutionary history of th

202 genomes from 3 locations, we demonstrate the biogeographical structure of the pan-genome of this spec

203 , we assessed the sampling quality of recent biogeographical studies.

204 at a scale unprecedented to date for fungal biogeographical studies.

205 distributional data are seldom available for biogeographical study or setting conservation priorities

206 socio-ecological importance, a comprehensive biogeographical synthesis of drylands is lacking.

207 In biogeographical terms, the realized niche has come to ex

208 que challenges and opportunities for testing biogeographical theories and macroecological laws.

209 However, biogeographical theory and global vegetation models poor

210 radients (LTG and ETG) play central roles in biogeographical theory, underpinning predictions of larg

211 According to broad-scale application of biogeographical theory, widespread retractions of specie

212 species richness, range size, endemicity and biogeographical transitions).

213 scaling relationships can explain the global biogeographical trend for smaller leaves in drier areas,

214 lecular markers have failed to reveal subtle biogeographical trends in Espeletia diversification, and

215 raphy-mass spectrometry for revealing subtle biogeographical trends in Espeletia diversification.

216 that viruses in modern microbialites display biogeographical variability and suggest that they may be

217 demonstrate the importance of incorporating biogeographical variability into predictive models for a

218 pecies' relation of survival to a key island-biogeographical variable.

219 uence of different climatic, topographic and biogeographical variables on alpha diversity also varies

220 ition of island biotas in relation to island biogeographical variables remains largely unknown.

221 f this exchange reveal very large functional biogeographical variation of climate-relevant ecosystem