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1 as a correlated character (a key premise of sympatric speciation).
2 e while selecting for ecotypes that maintain sympatric speciation.
3 s within the same host species, analogous to sympatric speciation.
4 models aiming to identify the conditions for sympatric speciation.
5 ence of male pregnancy: a predisposition for sympatric speciation.
6 These data support a model of recent sympatric speciation.
7 n and mate choices suggest ongoing incipient sympatric speciation.
8 ersity divergence, adaptation, and incipient sympatric speciation across life from viruses and bacter
9 rbivorous insects may be a first step toward sympatric speciation and can create new pests of agricul
10 ng-term BQ-stabilized coexistence, including sympatric speciation and the evolution of true mutualism
12 heoretical work supports the plausibility of sympatric speciation, but there remain few examples in w
13 so evaluate phylogenetic evidence bearing on sympatric speciation by asking whether tiny seahorse spe
15 nella sibling species complex is a model for sympatric speciation by means of host plant shifting.
18 hagoletis pomonella is a model for incipient sympatric speciation (divergence without geographic isol
20 This paper shows that a familiar model of sympatric speciation, driven by intraspecific competitio
22 ionary divergence is an example of incipient sympatric speciation from a single panmictic ancestral p
23 questions in evolutionary biology, including sympatric speciation, generalist versus specialist adapt
25 hat speciation without geographic isolation--sympatric speciation--has occurred within isolated islan
26 monella (Diptera: Tephritidae) is undergoing sympatric speciation (i.e., divergence without geographi
28 to a specific two-locus, two-allele model of sympatric speciation in a population occupying a two-nic
29 Does the paucity of empirical evidence of sympatric speciation in nature reflect reality, despite
33 these empirical findings to demonstrate that sympatric speciation indeed can occur under this mating
34 here more thorough testing is needed to move sympatric speciation into the realm of accepted scientif
35 trality, a finding consistent with models of sympatric speciation involving disruptive/divergent sele
38 hypergeometric phenotypic model to show that sympatric speciation is possible even when fitness and m
42 tDNA phylogenies support the plausibility of sympatric speciation, long considered a controversial me
44 n accumulating for ants [3, 5, 7, 9-12], but sympatric speciation remains controversial as a general
46 il and root microbes in a well-known case of sympatric speciation, the Howea palms of Lord Howe Islan
52 gly parsimonious hypothesis of 'contemporary sympatric speciation' via hybridization between octoploi
54 variable loci affecting fitness facilitates sympatric speciation, whereas the increase in the number
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