ライフサイエンスコーパス: sympatry

1 t radiations, colonization and speciation in sympatry.

2 s in which the species are known to occur in sympatry.

3 genetically isolated these species remain in sympatry.

4 ous and widespread distribution with partial sympatry.

5 eiotropy in facilitating rapid divergence in sympatry.

6 ting reproductive isolation and evolution in sympatry.

7 eference for calls of their natal lineage in sympatry.

8 ls of another species, both communicating in sympatry.

9 eciated from its host Mycocepurus goeldii in sympatry.

10 zation and causes assortative mating even in sympatry.

11 ther the same QTLs control flowering time in sympatry.

12 estrict interspecific gene flow in secondary sympatry.

13 otic isolation between two sister species in sympatry.

14 zation and causes assortative mating even in sympatry.

15 verlapping ranges, but rarely occur in close sympatry.

16 maintenance of ecological differentiation in sympatry.

17 mble the model less than do individuals from sympatry.

18 the accumulation of reproductive barriers in sympatry.

19 ations of vertebrates may become isolated in sympatry.

20 ow between chromosomal forms in this area of sympatry.

21 in bisexual species complexes that occur in sympatry.

22 that assortative mating has been enhanced in sympatry.

23 ted by evidence of reproductive isolation in sympatry.

24 ciculata and Ircinia variabilis that live in sympatry.

25 A low incidence of sympatry (0.6-0.7%) between wild B. rapa and cultivated

26 e parasite evolves directly from its host in sympatry [1-10].

27 o sites that represent different outcomes of sympatry: (1) a xeric mountain ridge where many hybrids

28 Our data suggest evolution in sympatry among populations of resource specialists.

29 ated with a reduction in prey consumption in sympatry and a segregation of prey according to prey siz

30 ch polyploid had at least partial geographic sympatry and abiotic niche overlap with one of its proge

31 s spretus), using samples from the ranges of sympatry and allopatry in Africa and Europe.

32 ce of predomestication cultivation, backyard sympatry, and spontaneous hybridization for the Mimosoid

33 into Q. chrysolepis in their current area of sympatry, and widespread admixture between the two linea

34 ts, and instead show that rates of secondary sympatry are positively associated with both the phyloge

35 ion in rates of hybridization among zones of sympatry between a pair of species provides a useful win

36 to the two parental species in two zones of sympatry between Ipomopsis aggregata and I. tenuituba, u

37 that might prove to be common, divergence in sympatry can be driven by sexual conflict or by associat

38 e panmictic ancestral population, or whether sympatry could have resulted from multiple colonisations

39 This suggests that climate-driven sympatry does not necessarily result in competitive excl

40 ctions constrain the transition to secondary sympatry following speciation.

41 requencies at sites where the forms occur in sympatry have led to the suggestion that these forms rep

42 d C. philodice are sister species with broad sympatry in North America.

43 Long sympatry in Siberia suggests that humans may be best see

44 of 36 individuals collected from an area of sympatry in Tabasco, Mexico.

45 e allopatric except for two known regions of sympatry in Texas and Mexico.

46 ariants and selection pressures unrelated to sympatry in the initial formation of these classic verte

47 ee ecotypes of killer whale occur in partial sympatry in the North Pacific.

48 ecause they have been proposed to diverge in sympatry (in the absence of geographic isolation) by shi

49 Thus, transition rates to sympatry increase with time since divergence and acceler

50 -wide trend of increased shared variation in sympatry, indicative of pervasive interspecific gene flo

51 limited co-existence, whereas more extensive sympatry is contingent on additional factors such as eco

52 often occur in species-rich assemblages, and sympatry is thought to be facilitated primarily by low d

53 Climate-driven sympatry may lead to competition for food resources betw

54 vation, and resulted in extensive artificial sympatry of 2-6 species locally and 13 species in total.

55 discovery provides new evidence for ecologic sympatry of large allosauroids and small-bodied tyrannos

56 gotes at these three sites, even in areas of sympatry of the two ITS types.

57 workers and queens is found only in areas of sympatry of the two species, and thus appears to arisen

58 gnised) speciation events preceded secondary sympatry of these cryptic species.

59 the development of reproductive barriers in sympatry or parapatry.

60 genetic differentiation between ecomorphs in sympatry, reflected primarily in elongated versus high-b

61 ocal host-pathogen coevolution and secondary sympatry, resulting in local shifting of parasite lineag

62 ympatric speciation must demonstrate species sympatry, sister relationships, reproductive isolation,

63 species' songs are perceived differently in sympatry than in allopatry.

64 When evolving on both hosts together (sympatry), the viruses split into two lineages with dive

65 Under divergent selection in sympatry, the genomes of incipient species become tempor

66 ely related taxa that occur in allopatry; in sympatry, the stabilizing forces that promote niche cons

67 evidence suggesting that mimics migrate from sympatry, where mimicry is favoured, to allopatry, where

68 by evidence that the two species coexist in sympatry, where preliminary data suggest reproductive ch

69 ong hosts suggest that chimpanzees living in sympatry with gorillas have acquired bacteria from goril

70 ly due to their reduced niche widths when in sympatry with other species, facilitating their coexiste

71 on from other varieties despite occurring in sympatry with other varieties and likely evolved from a

72 ty in the plant Phlox drummondii in areas of sympatry with the closely related species Phlox cuspidat

73 Newly formed tetraploid plants in sympatry with their diploid progenitors should face sign

74 patry), batesian mimics should occur only in sympatry with their model.

75 nt genetically determined morphs co-occur in sympatry within the same population) and geographic vari