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A new species of the genus Lasianobia Hampson, 1905, Lasianobia nainysi Saldaitis, Volynkin Zahiri, sp. nov. is described from highlands of western Sichuan Province of China. The new species is closely related to Lasianobia albilinea (Draudt, 1950). Adults, male and female genitalia as well as DNA barcode data of the new and related species are presented.Two Lophocampa species previously known only by females are paired with morphologically highly different male specimens. This pairing was initiated after the discovery of a mosaic gynandromorph specimen and then confirmed using the mitochondrial COI gene (the so-called DNA barcode). Following the discovery of a labeling error by Rothschild during the original description of two species, two recombinations are proposed. Pairs for each species are illustrated and the male specimens are described for the first time.Two new species of the genus Chelidoperca are described from specimens collected in 2015 and 2018 from the Andaman Sea, off the coast of Myanmar during trawl bottom surveys conducted by the R/V Dr. Fridtjof Nansen. Chelidoperca myathantuni sp. nov. is described based on 15 specimens (74.3-129.5 mm SL) from 101-185 m depth, which can be distinguished from all congeners by the following combination of characters 3 (2 full-sized plus 1 half-sized) scale rows between lateral line and middle of spinous dorsal-fin base; 42-44 (modally 44) pored lateral-line scales; 16 pectoral-fin rays; interorbital scales extending to mid-orbit level; scales on ventral surface of lower jaw restricted to the angular (not extending onto the dentary); enlarged caniniform teeth on the upper jaw; side of body with longitudinal dashed black stripe; dorsal fin pale yellow with reddish pigment mostly restricted at base of spines and rays. Chelidoperca flavimacula sp. nov. is described based on eight specimens (49.7-70.7 mm SL) from 84-131 m depth, which can be distinguished from all congeners by the following combination of characters 3 (2 full-sized plus 1 half-sized) scale rows between lateral line and middle of spinous dorsal-fin base; 42-45 (modally 42) pored lateral-line scales; 9-10 (modally 10) scale rows below the lateral line; 6 predorsal scales; 16-17 (modally 16) circumpeduncular scales; 5 scales rows on cheek; interorbital scales extending to mid-orbit level; anal fin with yellowish distal margin and three or four rows of bright yellow spots over its proximal half.This study revised the spider genus Oxyopes Latreille, 1804 in Taiwan and delineated the species boundaries based on morphological and molecular characters. A total of seven Oxyopes spiders were recognized, including two newly described species, O. hasta sp. nov. and O. taiwanensis sp. nov. Oxyopes fujianicus Song Zhu 1993 from Yilan County, Nantou County, and Kaohsuing City, and O. striagatus Song 1999 from New Taipei City, Taichung City, Nantou County, and Kaohsiung City were recorded for the first time in Taiwan. An identification key and a distributional map of Taiwanese Oxyopes species were provided. Partial COI sequences were obtained for molecular phylogenetic and species delimitation analyses. Maximum likelihood and Bayesian phylogenies, and DNA barcoding gap analysis supported morphologically defined species. However, molecular species delimitation based on Automatic Barcode Gap Discovery (ABGD), PID (Liberal), and generalized mixed Yule coalescent (GMYC) were incongruent in species assignment. The results showed that the interspecific genetic divergence between O. sertatus and O. taiwanensis was relatively low (1.28 ± 0.43%), and the intraspecific genetic divergence of O. striagatus was relatively high (1.69 ± 0.35%). Ecological data, additional samples and genetic loci are required to further examine the level of reproductive isolation and patterns of population genetic structure in Taiwanese Oxyopes.The Empis (Enoplempis) mira species group is revised and includes the type species of Enoplempis and four new species (E. macdonaldi sp. nov., E. submira sp. R428 purchase nov., E. williamturneri sp. nov., E. winkleri sp. nov.). A lectotype is designated for Enoplempis mira Bigot. The species group is defined by the yellow body colour, directionally asymmetrical male hindlegs and geniculate hindlegs in both males and females. The group has not been found outside of western North America and is known from California, Oregon, Idaho and Washington.The diversity of Panophrys horned toads is considered highly underestimated with a large number of undescribed cryptic species. In this work, we describe four Panophrys species from eastern China which were proposed as cryptic species by molecular data in previous study, additionally provide new information on the biogeography of these four species. Panophrys daiyunensis sp. nov. from southern Fujian, Panophrys daoji sp. nov. from eastern Zhejiang, Panophrys sanmingensis sp. nov. from the hilly area among Fujian, Jiangxi and Guangdong, and Panophrys tongboensis sp. nov. from northeastern Jiangxi, can be distinguished from all recognized congeners by a combination of morphological characteristics. The descriptions of these four new species take the recognized species of Panophrys to 51, which is the largest genus within the Asian horned toads subfamily Megophryinae. Considered as an appropriate arrangement for the Asian horned toads currently and applied in this study to describe the new species, the generic recognition of Panophrys is also discussed.DNA barcoding based on a fragment of mitochondrial Cytochrome C Oxidase subunit 1 gene (COI) was applied to the two chironomids Clunio balticus Heimbach (690 base pairs) and C. ponticus Michailova (691 base pairs). The two species differed by one deletion in the nucleotide sequence Adenine. However, the 658-nucleotide long sequences of DNA from the mitochondrial Cytochrome C Oxidase subunit 1 gene (COI) of C. balticus and C. ponticus were identical upon comparison. Further, they compared with homologous sequences for C. marinus Holiday and C. tsushimensis Tokunaga from the Barcode of Life (BOLD) database and the results plotted as a weighted graph, where C. tsushimensis, C. marinus and C. balticus C. ponticus formed three almost equidistant groups. From this, we established that the genetic distance between the respective COI sequences of C. balticus and C. ponticus is minimal, indicating a close relationship between the species indicative of recent common origin. However, the comparative analysis between C. tsushimensis, C.
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