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...|McLuckie A}}, {{aut|Lamb T}}, {{aut|Schwable C}}, {{aut|McCord R}} (1999) Genetic and morphological assessment of an unusual tortoise (''Gopherus agassizii''
...s by size, sex, and age of the tortoise. All future studies should include genetic documentation of non-hybrid specimens.
27 KB (3,863 words) - 17:46, 28 June 2011
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...available from present work to confirm it. The phylogenetic inferences and genetic distances agree on the establishment of ''{{Taxon name|Calisto smintheus}}'
29 KB (4,369 words) - 14:48, 13 January 2012
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...4X.1995.tb00228.x 10.1111/j.1365-294X.1995.tb00228.x]</ref > confirmed the genetic distinctiveness of this stand compared with the Willapa Bay population, sup
...a-Rossi D}}, {{aut|Davis H}}, {{aut|Strong D}} (1999) Extent and degree of hybridization between exotic (''Spartina alterniflora'') and native (''Spartina foliosa''
56 KB (8,258 words) - 16:39, 21 March 2012
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...Misset M}}, {{aut|Gourret J}}, {{aut|Bayer R}} (2003) Genetic evidence for hybridization between the native Spartina maritima and the introduced ''Spartina alternif
...Misset M}}, {{aut|Gourret J}}, {{aut|Bayer R}} (2003) Genetic evidence for hybridization between the native Spartina maritima and the introduced ''Spartina alternif
36 KB (5,153 words) - 16:44, 21 March 2012
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...t {{Taxon name|Poa annua|''Poa annua''}}, a tetraploid species, arose from hybridization between two Eurasian diploid species, {{Taxon name|Poa infirma|''Poa infirm
8 KB (1,096 words) - 19:18, 8 March 2015
- Draft:Test2/Effectively incorporating selected multimedia content into medical publications
- Draft:Jgmorse/Effectively incorporating selected multimedia content into medical publications
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...Several of these variants may constitute good species, but I believe more genetic and distribution data are needed (especially from Panama and South America)
...veral factors, including phenotypic plasticity, morphological convergence, hybridization, and sampling bias. It could also be that if the group represents a recent
42 KB (6,405 words) - 09:14, 24 April 2013
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...culation that differences in phenotypes of the two subspecies may indicate genetic isolation (Hubbs 1967).
...nd Brazos and other drainages to the north. It also could be the result of genetic drift producing different meristic frequencies in the various drainages. Th
23 KB (3,449 words) - 06:02, 8 July 2014
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...ref name="B133">{{aut|Nason J}}, {{aut|Hamrick J}} (1997) Reproductive and genetic consequences of forest fragmentation: Two case studies of Neotropical canop
...veral other species suggests the possibility that this species is prone to hybridization (see discussion above in sections treating the genus as a whole).
42 KB (6,135 words) - 13:42, 10 April 2017
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...a variant of ''{{Taxon name|Spondias tuberosa}}'' unless and until further genetic/molecular investigations suggest otherwise.<br />
28 KB (4,113 words) - 13:42, 10 April 2017
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...|McLuckie A}}, {{aut|Lamb T}}, {{aut|Schwalbe C}}, {{aut|McCord R}} (1999) Genetic and morphometric assessment of an unusual tortoise (''{{Taxon name|Gopherus
...|McLuckie A}}, {{aut|Lamb T}}, {{aut|Schwalbe C}}, {{aut|McCord R}} (1999) Genetic and morphometric assessment of an unusual tortoise (''{{Taxon name|Gopherus
34 KB (4,763 words) - 18:16, 10 February 2016
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...lankton genus Holopedium (Crustacea: Branchiopoda: Ctenopoda), revealed by genetic methods
...axon name|Holopedium gibberum|''H. gibberum''}}, again with no evidence of hybridization.
7 KB (969 words) - 06:52, 7 April 2016
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...lankton genus Holopedium (Crustacea: Branchiopoda: Ctenopoda), revealed by genetic methods
...these two species have allopatric distributions reducing the likelihood of genetic exchange (Fig. 4 c,e). {{Taxon name|Holopedium atlanticum|''Holopedium atla
10 KB (1,330 words) - 06:53, 7 April 2016
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...83894 ({{Taxon name|Elops smithi|''E. smithi''}}, haplotypes C – N). The genetic difference (d) between the {{Taxon name|Elops saurus|''E. saurus''}} haplot
TABLE2. Data associated with fish used in the genetic analysis. Collection date and locale are listed, along with standard length
15 KB (1,845 words) - 20:02, 8 April 2016
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...t presents a starting hypothesis for a much needed study on the population genetic level of the {{Taxon name|Crematogaster hova|''C. hova''}} - complex.
...more and more in ants (e.g. Feldhaar, 2008; Korczynska et al., 2010), and hybridization has already been posited to occur in members of the subgenus {{Taxon name|C
28 KB (3,780 words) - 05:49, 11 April 2016
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...region and the cytochrome b gene were used for phylogeny construction. The genetic distance separating the three guppy taxa is 0,0 29. This is well in the ran
P. o b s c u r a is endemic to the island of [[Trinidad]]. A genetic divergence of the guppies from the Oropuche drainage has been noted earlier
32 KB (4,737 words) - 05:16, 20 April 2016
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Intraspecific corrected genetic divergences varied from 0 to 2.1 (excluding CNIN573), 0.27 to 3.18 and 0 to
...is incomplete lineage sorting or hybridization. Further morphological and genetic studies will help to confirm the taxonomic status of the populations of ''{
9 KB (1,236 words) - 16:58, 16 May 2016
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...mitochondrial genome of koupreys seems to have been transferred by natural hybridization into the ancestor of Cambodian bantengs. The taxonomic status of koupreys i
24 KB (2,840 words) - 16:18, 30 August 2016
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...lade brings up the possibility of that clade Acre 0 1 originated from past genetic introgression from the widely distributed clade Acre 0 2 into {{Taxon name|
...divergent sequences found within clade femo 0 4 suggest elevated levels of genetic variability between populations across the Peruvian Amazon, and additional
42 KB (5,660 words) - 09:05, 7 December 2016
