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data/03/E0/55/03E0551FFFCE990A31F5F90AFDA8BBF0.ttl
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@prefix trt: <http://plazi.org/vocab/treatment#> .
<http://treatment.plazi.org/id/03E0551FFFCE990A31F5F90AFDA8BBF0>
cito:cites <http://dx.doi.org/10.5281/zenodo.14047621>, <http://dx.doi.org/10.5281/zenodo.14047617>, <http://dx.doi.org/10.5281/zenodo.14047619>, <http://dx.doi.org/10.5281/zenodo.14047623> ;
cito:cites <http://dx.doi.org/10.5281/zenodo.14047621>, <http://dx.doi.org/10.5281/zenodo.14047617>, <http://dx.doi.org/10.5281/zenodo.14047619>, <http://dx.doi.org/10.5281/zenodo.14107798>, <http://dx.doi.org/10.5281/zenodo.14047623> ;
dc:creator "Khan, Gulzar; Mayland-Quellhorst, Eike; Kosachev, Petr A.; Mandáková, Terezie; Lysak, Martin A.; Albach, Dirk C." ;
dc:title "Veronica (Pseudolysimachium)" ;
trt:publishedIn <http://dx.doi.org/10.1002/tax.13176> ;
@ -26,7 +26,7 @@
dc:creator "Khan, Gulzar; Mayland-Quellhorst, Eike; Kosachev, Petr A.; Mandáková, Terezie; Lysak, Martin A.; Albach, Dirk C." ;
dc:date "2024" ;
dc:title "Altai Mountains - cradle of hybrids and introgressants: A case study in Veronica subg. Pseudolysimachium (Plantaginaceae)" ;
fabio:hasPart <http://dx.doi.org/10.5281/zenodo.14047621>, <http://dx.doi.org/10.5281/zenodo.14047617>, <http://dx.doi.org/10.5281/zenodo.14047619>, <http://dx.doi.org/10.5281/zenodo.14047623> ;
fabio:hasPart <http://dx.doi.org/10.5281/zenodo.14047621>, <http://dx.doi.org/10.5281/zenodo.14047617>, <http://dx.doi.org/10.5281/zenodo.14047619>, <http://dx.doi.org/10.5281/zenodo.14107798>, <http://dx.doi.org/10.5281/zenodo.14047623> ;
a fabio:JournalArticle .
<http://taxon-name.plazi.org/id/Plantae/Veronica_Pseudolysimachium>
@ -91,6 +91,11 @@
fabio:hasRepresentation <https://zenodo.org/record/14047619/files/figure.png> ;
a fabio:Figure .
<http://dx.doi.org/10.5281/zenodo.14107798>
dc:description "Fig. 4. STRUCTURE results showing the probability of ancestry of each individual (horizontal axis) to each of K = 2 populations (vertical axis) in all the five scenarios. A, Veronica spicata × V. pinnata; B, V. incana and V. longifolia; C, V. longifolia and V. porphyriana; D & E, V. pinnata and V. porphyriana involving putative hybrids of V. ×schmakovii and V. ×sessiliflora. Details of the exact posterior probabilities of each putative hybrid individual and their corresponding parents are given in suppl. Table S3." ;
fabio:hasRepresentation <https://zenodo.org/record/14107798/files/figure.png> ;
a fabio:Figure .
<http://dx.doi.org/10.5281/zenodo.14047623>
dc:description "Fig. 5. Results of the G-PhoCS analysis for effective population sizes, and gene flow using only pure individuals (no admixture). The inferred current effective population size (Ne) of each species are given for all the five species. The direction of the arrows represents the probability of migration among the species both in forward and reverse directions. The width of the bars represents the effective population size of each species. For population size estimation, we used the equations Ne (effective population size) = θ / 4μg; and T (divergence time) = τ · g / μ; where substitution rate/site/year (μ) = 2.44E-9, generation time for population (g) = 10 years. Migration rates are based on per generation parameter (Msx = msx · θx / 4), which is the proportion of individuals in population x arrived by migration from another population per generation. Gene flow has been calculated using the total migration rate, cases where the total rate is low, it approximates the probability of gene flow between the two species. However, for higher rates, we adjusted probabilities into rates with the equation P = 1 − e−m (where P = the probability of gene flow, e = exponent, and m = total migration rate; following vonHoldt & al., 2016). The phylogenetic tree on which the G-PhoCS analysis has been based is given in suppl. Fig. S2. For complete details, see in Materials and Methods as well as suppl. Tables S4 and S5 for migration rates (msx), τ and θ values, and divergence times." ;
fabio:hasRepresentation <https://zenodo.org/record/14047623/files/figure.png> ;