ライフサイエンスコーパス: biogeographical

1 While biogeographical algorithms using next-generation sequenc

2 Biogeographical analyses suggest that Evacanthinae origi

3 Biogeographical analyses suggest that local mainstem ele

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

5 The biogeographical analysis localised proto-Druze to the mo

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

7 Biogeographical and ecological theory suggests that spec

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

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

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

11 Insight on the biogeographical and phenotypic variations of Cacospongia

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

28 Although biogeographical differences in community assembly mechan

29 We suggest that biogeographical differences in the relative importance o

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

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

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

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

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

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

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

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

38 l issues of developmental, morphological and biogeographical evolution.

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

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

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

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

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

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

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

46 The biogeographical history of the north-south divergence ev

47 lifornian golden cup oaks with an intriguing biogeographical history.

48 onary units and infer their evolutionary and biogeographical history.

49 lationships and associated morphological and biogeographical hypotheses.

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

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

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

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

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

55 Classical biogeographical observations suggest that ecosystems are

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

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

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

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

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

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

62 In contrast to biogeographical patterns of planktonic marine microbial

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

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

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

66 Biogeographical, physiological, and paleoecological evid

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

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

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

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

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

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

73 three freshwater wetlands that span multiple biogeographical provinces.

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

75 Biogeographical regions (geographically distinct assembl

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

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

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

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

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

81 eving a larger number of commonly recognized biogeographical regions.

82 perience rapid climate-driven changes across biogeographical regions.

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

84 Biogeographical shifts are a ubiquitous global response

85 These biogeographical shifts are in agreement with recent chan

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

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

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

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

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

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

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

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

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

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

96 However, biogeographical theory and global vegetation models poor

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

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

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

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

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

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

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

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