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1 as a correlated character (a key premise of sympatric speciation).
2 n and mate choices suggest ongoing incipient sympatric speciation.
3 e while selecting for ecotypes that maintain sympatric speciation.
4 s within the same host species, analogous to sympatric speciation.
5 isolation mechanisms that underlie incipient sympatric speciation.
6 models aiming to identify the conditions for sympatric speciation.
7 ence of male pregnancy: a predisposition for sympatric speciation.
8 These data support a model of recent sympatric speciation.
9 ersity divergence, adaptation, and incipient sympatric speciation across life from viruses and bacter
10 rbivorous insects may be a first step toward sympatric speciation and can create new pests of agricul
12 ng-term BQ-stabilized coexistence, including sympatric speciation and the evolution of true mutualism
14 e evolution of inquiline social parasites by sympatric speciation but cannot exclude the alternative,
15 heoretical work supports the plausibility of sympatric speciation, but there remain few examples in w
16 so evaluate phylogenetic evidence bearing on sympatric speciation by asking whether tiny seahorse spe
18 nella sibling species complex is a model for sympatric speciation by means of host plant shifting.
20 c speciation is dominant, and while frequent sympatric speciation cannot be discounted, the most like
22 hagoletis pomonella is a model for incipient sympatric speciation (divergence without geographic isol
24 This paper shows that a familiar model of sympatric speciation, driven by intraspecific competitio
26 ionary divergence is an example of incipient sympatric speciation from a single panmictic ancestral p
27 questions in evolutionary biology, including sympatric speciation, generalist versus specialist adapt
29 absence of geographic barriers to gene flow (sympatric speciation)-has puzzled evolutionary biologist
30 hat speciation without geographic isolation--sympatric speciation--has occurred within isolated islan
31 monella (Diptera: Tephritidae) is undergoing sympatric speciation (i.e., divergence without geographi
33 to a specific two-locus, two-allele model of sympatric speciation in a population occupying a two-nic
34 Does the paucity of empirical evidence of sympatric speciation in nature reflect reality, despite
38 these empirical findings to demonstrate that sympatric speciation indeed can occur under this mating
39 here more thorough testing is needed to move sympatric speciation into the realm of accepted scientif
40 trality, a finding consistent with models of sympatric speciation involving disruptive/divergent sele
44 hypergeometric phenotypic model to show that sympatric speciation is possible even when fitness and m
48 tDNA phylogenies support the plausibility of sympatric speciation, long considered a controversial me
49 X speciation island lends further support to sympatric speciation models facilitated by pericentric r
51 gently selected traits can influence whether sympatric speciation occurs(4), but empirical tests of t
52 r reproductive timing is a magic trait for a sympatric speciation process, as it is both ecologically
53 n accumulating for ants [3, 5, 7, 9-12], but sympatric speciation remains controversial as a general
55 il and root microbes in a well-known case of sympatric speciation, the Howea palms of Lord Howe Islan
61 gly parsimonious hypothesis of 'contemporary sympatric speciation' via hybridization between octoploi
63 variable loci affecting fitness facilitates sympatric speciation, whereas the increase in the number