ライフサイエンスコーパス: biogeography

1 development of theories of biodiversity and biogeography.

2 inferences of terrestrialization history and biogeography.

3 ic evolution, divergence time estimation and biogeography.

4 limits is a promising approach in functional biogeography.

5 sights into their life history evolution and biogeography.

6 e spatial scales for understanding microbial biogeography.

7 plotypes challenge predictions of vicariance biogeography.

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

9 solved questions in evolutionary biology and biogeography.

10 ty gradients dates back to the foundation of biogeography.

11 inferences about their ancestry and historic biogeography.

12 into marine actinobacterial biodiversity and biogeography.

13 biogeological functioning, biodiversity, and biogeography.

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

15 ts had an important early influence on their biogeography.

16 y reversing the classical scenario of oscine biogeography.

17 need to understand how climate is linked to biogeography.

18 t case for examining bacterial diversity and biogeography.

19 s the subjects of bacterial biodiversity and biogeography.

20 interpreting patterns of macroevolution and biogeography.

21 erstanding of placental mammal evolution and biogeography.

22 n species distribution leading to changes in biogeography.

23 scape genetics under the more general field: biogeography.

24 nutrient availability to control microbiota biogeography.

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

26 oor sediments may have distinctive bacterial biogeography.

27 for example, in mutation rates or historical biogeography.

28 or process-based modeling approaches to tree biogeography.

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

30 oceanic islands is a central theme of island biogeography.

31 ogists since Darwin's earliest insights into biogeography.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

47 Biogeography and individuality shape the structural and

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

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

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

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

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

53 indicating interspecific concordance between biogeography and phylogeography.

54 providing intraspecific concordance between biogeography and phylogeography.

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

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

57 Dinoflagellate biogeography and sea surface temperature paleothermometr

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

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

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

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

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

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

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

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

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

67 Studies of biogeography are important for understanding biodiversit

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

69 Island biogeography as applied to communities separated by time

70 This process is referred to in biogeography as vicariance.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

111 Moreover, anole biogeography increasingly reflects anthropogenic rather

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

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

114 Countryside biogeography is an alternative framework, which recogniz

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

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

117 Historical biogeography is dominated by vicariance methods that sea

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

119 Island biogeography is fundamental to understanding colonizatio

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

141 Elucidating the biogeography of bacterial communities on the human body

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

161 The global biogeography of microorganisms remains largely unknown,

162 The biogeography of phages has only recently been investigat

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

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

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

166 The biogeography of Streptomyces was examined at regional sp

167 c processes have influenced the contemporary biogeography of Streptomyces.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

182 The functional biogeography of tropical forests is expressed in foliar

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

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

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

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

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

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

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

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

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

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

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

194 Functional biogeography provides a framework to address how ecosyst

195 Their biogeography provides essential clues to their cryptic r

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

211 Island biogeography theory indicates that, where the average ti

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

213 pected biodiversity patterns based on island biogeography theory.

214 st how this evolutionary history fits island biogeography theory.

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

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

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

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

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

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

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

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

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

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