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1 the field and in two contexts (allopatry vs. sympatry).
2  that present intermediate forms in areas of sympatry.
3 roductive isolation could gradually arise in sympatry.
4 but their contributions were more similar in sympatry.
5 shown that this process occurred in complete sympatry.
6 al vertebrate pattern of steadily increasing sympatry.
7 d in the context of speciation and secondary sympatry.
8 cally related species that use camouflage in sympatry.
9 iation, with no evidence of hybridization or sympatry.
10  result from enhanced divergent selection in sympatry.
11 ood of species coexistence from allopatry to sympatry.
12 logy traits, though mainly in individuals in sympatry.
13 or 10% (palms) of speciation events occur in sympatry.
14 ce corresponding to host preference, even in sympatry.
15 ities shared with defended species living in sympatry.
16 t radiations, colonization and speciation in sympatry.
17 s in which the species are known to occur in sympatry.
18 s can promote rapid and stable speciation in sympatry.
19 ciculata and Ircinia variabilis that live in sympatry.
20 genetically isolated these species remain in sympatry.
21 ous and widespread distribution with partial sympatry.
22 eiotropy in facilitating rapid divergence in sympatry.
23 ting reproductive isolation and evolution in sympatry.
24 eference for calls of their natal lineage in sympatry.
25 ls of another species, both communicating in sympatry.
26 eciated from its host Mycocepurus goeldii in sympatry.
27 zation and causes assortative mating even in sympatry.
28 ther the same QTLs control flowering time in sympatry.
29 estrict interspecific gene flow in secondary sympatry.
30 otic isolation between two sister species in sympatry.
31 zation and causes assortative mating even in sympatry.
32 verlapping ranges, but rarely occur in close sympatry.
33 maintenance of ecological differentiation in sympatry.
34 mble the model less than do individuals from sympatry.
35 the accumulation of reproductive barriers in sympatry.
36 ations of vertebrates may become isolated in sympatry.
37 ow between chromosomal forms in this area of sympatry.
38  in bisexual species complexes that occur in sympatry.
39 that assortative mating has been enhanced in sympatry.
40 ted by evidence of reproductive isolation in sympatry.
41                           A low incidence of sympatry (0.6-0.7%) between wild B. rapa and cultivated
42 e parasite evolves directly from its host in sympatry [1-10].
43 o sites that represent different outcomes of sympatry: (1) a xeric mountain ridge where many hybrids
44 tic proximity and ecological interactions in sympatry, acting on macroevolutionary patterns of phenot
45                Our data suggest evolution in sympatry among populations of resource specialists.
46        Our models show that the incidence of sympatry among sister pairs rises rapidly within the fir
47 ated with a reduction in prey consumption in sympatry and a segregation of prey according to prey siz
48 ch polyploid had at least partial geographic sympatry and abiotic niche overlap with one of its proge
49 s spretus), using samples from the ranges of sympatry and allopatry in Africa and Europe.
50 integrity of reproductive isolation while in sympatry and allopatry, then characterized hybrid ancest
51 es were significantly differentiated in both sympatry and allopatry.
52  demonstrated strong size dimorphism when in sympatry and can be linked to differing developmental mo
53 n occurs broadly while introgression acts in sympatry and drift when the population sizes decrease.
54 t primate radiation, exhibit high degrees of sympatry and form multi-species groups.
55 ce of predomestication cultivation, backyard sympatry, and spontaneous hybridization for the Mimosoid
56 ness of sexual and asexual taxa currently in sympatry, and to analyse the evolutionary consequences o
57 into Q. chrysolepis in their current area of sympatry, and widespread admixture between the two linea
58  antipredator traits between the species: in sympatry, antipredator adaptations were relatively incre
59              Cryptic species that coexist in sympatry are likely to simultaneously experience strong
60                      Two species breeding in sympatry are more likely to coexist if their ecological
61 ts, and instead show that rates of secondary sympatry are positively associated with both the phyloge
62 eported in closely related species living in sympatry as a result of reproductive character displacem
63                          We used this recent sympatry as an opportunity to investigate how dynamic lo
64 e undergoing extensive gene flow in areas of sympatry at range peripheries.
65 ed several disparate proboscidean species in sympatry became commonplace.
66 ion in rates of hybridization among zones of sympatry between a pair of species provides a useful win
67 cent climate change has created new foraging sympatry between Adelie (Pygoscelis adeliae) and gentoo
68 s changed consistently between allopatry and sympatry between drainages, the magnitude of the size-de
69  to the two parental species in two zones of sympatry between Ipomopsis aggregata and I. tenuituba, u
70 e responses should slow the establishment of sympatry between recently diverged forms.
71           Here, we investigate the effect of sympatry between species on the convergence vs. divergen
72                         The establishment of sympatry between these species provided the opportunity
73 on was either absent (allopatry) or maximal (sympatry), but was much reduced at intermediate rates (p
74 that might prove to be common, divergence in sympatry can be driven by sexual conflict or by associat
75                               Conversely, in sympatry, carp isotopic niches were always considerably
76 e panmictic ancestral population, or whether sympatry could have resulted from multiple colonisations
77  then presented the species in allopatry and sympatry, determining the changes in their trophic (isot
78                                           In sympatry, divergence was mainly mediated by novel mutati
79            This suggests that climate-driven sympatry does not necessarily result in competitive excl
80 species have evolved or currently coexist in sympatry due to differential adaptation in a heterogeneo
81 s, suggesting that species failing to attain sympatry early tend to remain allopatric.
82 ctions constrain the transition to secondary sympatry following speciation.
83 d trait differences that will likely promote sympatry from those that likely will not, and we discuss
84 requencies at sites where the forms occur in sympatry have led to the suggestion that these forms rep
85  divergence driven by costly interactions in sympatry (i.e., 'character displacement').
86 nal selection during the incipient stages of sympatry in a new community that corresponds to repeated
87 ater Ardenna pacifica (WTS) when breeding in sympatry in a tropical area.
88 ow that species recognition evolved prior to sympatry in A. oculatus.
89 d C. philodice are sister species with broad sympatry in North America.
90                                         Long sympatry in Siberia suggests that humans may be best see
91  of 36 individuals collected from an area of sympatry in Tabasco, Mexico.
92 e allopatric except for two known regions of sympatry in Texas and Mexico.
93 ariants and selection pressures unrelated to sympatry in the initial formation of these classic verte
94 ee ecotypes of killer whale occur in partial sympatry in the North Pacific.
95 ecause they have been proposed to diverge in sympatry (in the absence of geographic isolation) by shi
96                    Thus, transition rates to sympatry increase with time since divergence and acceler
97 -wide trend of increased shared variation in sympatry, indicative of pervasive interspecific gene flo
98 limited co-existence, whereas more extensive sympatry is contingent on additional factors such as eco
99 sted during the Late Triassic, their limited sympatry is currently unexplained, indicating that ecolo
100 often occur in species-rich assemblages, and sympatry is thought to be facilitated primarily by low d
101 ers prevent niche divergence or selection in sympatry is too weak to overcome gene flow from allopatr
102 ushroom-forming fungi tend to be stronger in sympatry, leading to speculation on whether they are bei
103                               Climate-driven sympatry may lead to competition for food resources betw
104                    For example, a history of sympatry might correspond with divergence.
105 vation, and resulted in extensive artificial sympatry of 2-6 species locally and 13 species in total.
106 dy size or may also result from long-lasting sympatry of gazelles and cattle - first wild and later d
107 discovery provides new evidence for ecologic sympatry of large allosauroids and small-bodied tyrannos
108 gotes at these three sites, even in areas of sympatry of the two ITS types.
109 workers and queens is found only in areas of sympatry of the two species, and thus appears to arisen
110 gnised) speciation events preceded secondary sympatry of these cryptic species.
111  on nearly identical colours and patterns in sympatry, often to avoid predation by mimicking noxious
112 ait divergence is a general prerequisite for sympatry or a consequence of interactions between sympat
113 hat new species in this genus have formed in sympatry or parapatry, with occasional hybridisation bet
114  the development of reproductive barriers in sympatry or parapatry.
115 outcomes-speciation reversal, parapatry, and sympatry putatively through reproductive character displ
116 genetic differentiation between ecomorphs in sympatry, reflected primarily in elongated versus high-b
117 ocal host-pathogen coevolution and secondary sympatry, resulting in local shifting of parasite lineag
118                                      Even in sympatry, samples with different karyomorphs differ more
119 ympatric speciation must demonstrate species sympatry, sister relationships, reproductive isolation,
120 ecent rates of expansion of sister taxa into sympatry, slower rates of evolution of traits important
121                                              Sympatry, specifically, was preceded by substantial intr
122           We found phenotypic convergence in sympatry, stronger among distantly related species, whil
123  traits in closely-related species living in sympatry strongly depends on both shared selective press
124 er, carp isotopic niches were also larger in sympatry than allopatry.
125  species' songs are perceived differently in sympatry than in allopatry.
126 ion rates and are more likely to speciate in sympatry than less-virulent and nonparasitic relatives.
127        When evolving on both hosts together (sympatry), the viruses split into two lineages with dive
128                 Under divergent selection in sympatry, the genomes of incipient species become tempor
129 ely related taxa that occur in allopatry; in sympatry, the stabilizing forces that promote niche cons
130 t wherein lineages are unlikely to establish sympatry unless and until they evolve sufficient trait d
131 he sizes of the fishes between allopatry and sympatry using a substitutive experimental design.
132                       This pulse occurred as sympatry was established in western North America.
133 d areas of spinosaurid anatomy, suggest that sympatry was present and potentially common in baryonych
134 ecently and subsequently came into secondary sympatry where they form replicated contact zones.
135 evidence suggesting that mimics migrate from sympatry, where mimicry is favoured, to allopatry, where
136  by evidence that the two species coexist in sympatry, where preliminary data suggest reproductive ch
137 scence between M. helenor and M. achilles in sympatry, while the iridescence of M. helenor diverged i
138 monstrates that the two lineages can live in sympatry with ample opportunities to interbreed in a lar
139               In particular, we test whether sympatry with closely-related species leads to decreasin
140 ong hosts suggest that chimpanzees living in sympatry with gorillas have acquired bacteria from goril
141 led B. barbus growth rates were depressed in sympatry with L. idus.
142  release of the first MVs, the impact of the sympatry with LRs and their WRs has not been explored wi
143 ly due to their reduced niche widths when in sympatry with other species, facilitating their coexiste
144 on from other varieties despite occurring in sympatry with other varieties and likely evolved from a
145 ty in the plant Phlox drummondii in areas of sympatry with the closely related species Phlox cuspidat
146            Newly formed tetraploid plants in sympatry with their diploid progenitors should face sign
147 patry), batesian mimics should occur only in sympatry with their model.
148 nt genetically determined morphs co-occur in sympatry within the same population) and geographic vari

 
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