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Position of neck banded blenny Leptostichaeus pumilus (Perciformes: Zoarcoidei) in the system of the suborder Zoarcoidei as inferred from molecular genetic data
TLDR
Significant genetic differences between neck banded blenny and the family Stichaeidae correspond to the level of divergence between other families of the suborder Zoarcoidei (Zaproridae, Ptilichthyidae, Pholidae, Cryptacanthodidae, and Bathymasteridae).
Relationships and divergence of some taxa of the subfamily Lycodinae (Zoarcidae, Pisces) based on molecular-genetic and morphological data
TLDR
The problem of determination of the time of divergence of the studied zoarcid-like fish using the concept of “molecular clock” and its calibration according to paleontological and paleogeographic data is discussed.
Relationships and position of the genus Neozoarces of the subfamily neozoarcinae in the system of the suborder Zoarcoidei (Pisces, Perciformes) by molecular-genetic data
TLDR
The results of investigations confirm the viewpoint suggested by Makushok (1961) who included, for the first time, the subfamily Neozoarcinae to the family Zoarcidae on the basis of comparative morphological investigation of these groups.
Relationships and position of wrymouths of the family cryptacanthodidae in the system of the suborder Zoarcoidei (Pisces, Perciformes)
TLDR
The opinion of Makushok on a phylogenetically distinct position of wrymouths in relation to snake blennies and related families is not supported and the anatomical features of skull structure support the data of molecular genetics.
Relationships and position of the taxa of the subfamily Xiphisterinae in the system of the suborder Zoarcoidei (Perciformes)
TLDR
The genetic heterogeneity of Xiphisterinae and the propriety of its division into two subfamilies should be raised to the rank of a family and classified not within the superfamily Stichaeoidae but rather as independent taxa of the suborder Zoarcoidei.
Phylogenetic relations in the family pholidae (Perciformes: Zoarcoidei) based on genetic and morphological data
TLDR
Analysis of variation of genes of COI, cytochrome b, and 16S rRNA of mitochondrial DNA indicates different phylogenetic isolation of the family taxa.
Genetic structure of the sable Martes zibellina L. populations from Magadan oblast as inferred from mitochondrial DNA variation
TLDR
The observed spatial heterogeneity of the sable populations of Magadan oblast was explained in terms of the formation of the introduction foci of Kamchatka and Khabarovsk sables, starting from the 1950s.
Molecular genetic and karyological analysis of antlered sculpins of Enophrys diceraus group (Cottidae)
TLDR
It is concluded that E. diceraus from the Sea of Japan belongs to another species, most likely, E. namiyei.
Genetic differentiation of species and taxonomic structure of the superfamily Stichaeoidea (Perciformes: Zoarcoidei)
TLDR
These investigations suggest that the superfamily Stichaeoidea should include not only the families Sticaeidae, Pholidae, and Ptilichthyidae, but also the Zaproridae and Cryptacanthodidae, while the family Anarhichadidae should be excluded from it.
Phylogenetic relationships of blennies of the family Pholidae (Perciformes: Zoarcoidei) using the results of molecular genetic analysis
TLDR
It is proven that the idea to validate particular genera (or subgenera) Enedrias and Allopholis was fairly weak and they should be consid ered within the synonymy of the genus Pholis (Makushok, 1958).
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