The Polyommatus (Agrodiaetus) damone (Eversmann, 1841) species complex comprises from 5 to 8 species distributed in southeastern Europe and southern Siberia. Here we used chromosomal and DNA-barcode markers in order to test the taxonomic hypotheses previously suggested for this complex. We revealed that all taxa within this group demonstrate chromosomal stasis and share the same or very similar haploid chromosome number (n = 66 or n = 67). This finding is unexpected since the karyotypes are known to be very diverse and species-specific within the other taxa of the subgenus Agrodiaetus Hübner, 1822. Analysis of the mitochondrial gene revealed six diverged clusters of individuals within the complex. Each cluster has a specific geographic distribution and is characterized by distinct morphological features in the wing pattern. The clusters mostly (but not always) correlate with traditionally recognized species. As a result of our study, we describe a new subspecies P. (A.) iphigenides zarmitanus. from Uzbekistan and Tajikistan and show that the taxon originally described as Lycaena kindermanni var. melania Staudinger, 1886 represents a subspecies P. (A.) iphigenides melanius (Staudinger, 1886). Polyommatus (A.) samusi Korb, 2017 (.) and P. (A.) melanius komarovi Korb, 2017 (.) are considered here as junior subjective synonyms of P. (A.) iphigenides iphigenides (Staudinger, 1886).
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http://dx.doi.org/10.3897/compcytogen.v15.i1.60347 | DOI Listing |
A new species, Polycaena eckweileri sp. n., is described from Gansu Province, China.
View Article and Find Full Text PDFTaxon Rep Int Lepid Surv
October 2022
Department of Biochemistry, University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd., Dallas, TX 75390, USA.
The comparative genomics of butterflies yields additional insights into their phylogeny and classification that are compiled here. As a result, 3 genera, 5 subgenera, 5 species, and 3 subspecies are proposed as new, i.e.
View Article and Find Full Text PDFTaxon Rep Int Lepid Surv
May 2022
Department of Biophysics, University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd., Dallas, TX 75390-9050, USA.
Insecta mundi
February 2022
Howard Hughes Medical Institute and Departments of Biophysics and Biochemistry, University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd., Dallas, TX, 75390-9050 USA.
Our expanded efforts in genomic sequencing to cover additional skipper butterfly (Lepidoptera: Hesperiidae) species and populations, including primary type specimens, call for taxonomic changes to restore monophyly and correct misidentifications by moving taxa between genera and proposing new names. Reconciliation between phenotypic characters and genomic trees suggests three new tribes, two new subtribes, 23 new genera, 17 new subgenera and 10 new species that are proposed here: Psolosini Grishin, (type genus Staudinger, 1889), Ismini Grishin, (type genus Distant, 1886), Eetionini Grishin, (type genus de Nicéville, 1895), Orphina Grishin, (type genus Godman, 1901), Carystoidina Grishin, (type genus Godman, 1901), Grishin, (type species Plötz, 1882), Grishin, (type species Mabille and Boullet, 1912), Grishin, (type species Grishin, ), Grishin, (type species Plötz, 1884), Grishin, (type species Evans, 1937), Grishin, (type species Trimen, 1873), Grishin, (type species Hayward, 1951), Grishin, (type species Mabille, 1889), Grishin, (type species ? Schaus, 1913), Grishin, (type species Schaus, 1902), Grishin, (type species Schaus, 1902), Grishin, (type species Godman, 1900), Grishin, (type species Bell, 1937), Grishin, (type species Bell, 1932), Grishin, (type species Plötz, 1882), Grishin, (type species Bell, 1930), Grishin, (type species Bell, 1930), Grishin, (type species Bell, 1932), Grishin, (type species Lindsey, 1925), Grishin, (type species Hewitson, 1877), Grishin, (type species Godman, 1900), Grishin, (type species Hewitson, 1866), Grishin, (type species Hewitson, 1878), Grishin, (type species Evans, 1952), Grishin, (type species Cramer, 1780), Grishin, (type species Plötz, 1884), Grishin, (type species Plötz, 1884), Grishin, (type species Evans, 1928), Grishin, (type species Herrich-Schäffer, 1869), Grishin, (type species Mabille, 1891), Grishin, (type species [sic] Schaus, 1913), Grishin, (type species Godman, 1900), Grishin, (type species Möschler, 1879), Grishin, (type species Mielke and Casagrande, 2002), Grishin, (type species Godman, 1901), Grishin, (type species Schaus, 1902), Grishin, (type species Evans, 1955), Grishin, (type species Evans, 1955), Grishin, (type species Godman, 1900), Grishin, (type species Evans, 1955), Grishin, (type locality in Brazil: Santa Catarina), Grishin, (type locality in Guyana: Acarai Mts.), Grishin, (type locality in Paraguay: Sapucay), Grishin, (type locality in Brazil: Rondônia), Grishin, (type locality in Ecuador: Riobamba), Grishin, (type locality in Colombia: Bogota), Grishin, (type locality in Panama: Colón), Grishin, (type locality in Nicaragua: Chontales), Grishin, (type locality in Peru: Cuzco), and Grishin, (type locality in Costa Rica).
View Article and Find Full Text PDFTaxon Rep Int Lepid Surv
May 2021
Howard Hughes Medical Institute, University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd., Dallas, TX 75390-9050, USA.
Continuing with comparative genomic exploration of worldwide butterfly fauna, we use all protein-coding genes as they are retrieved from the whole genome shotgun sequences for phylogeny construction. Analysis of these genome-scale phylogenies projected onto the taxonomic classification and the knowledge about butterfly phenotypes suggests further refinements of butterfly taxonomy that are presented here. As a general rule, we assign most prominent clades of similar genetic differentiation to the same taxonomic rank, and use criteria based on relative population diversification and the extent of gene exchange for species delimitation.
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