Concordant differences in morphology, phenology and RAMS markers, as well as in sequenced mtDNA (COI, COII, cytb) and nuclear DNA (ITS2) fragments, indicate that Dolerus asper Zaddach, 1859 and Dolerus brevicornis Zaddach, 1859 are valid species. On the basis of morphology, molecular markers, and distributional records, both species are distinct from Dolerus gibbosus Hartig, 1837 (= Dolerus planatus Hartig, 1837). Taxonomy of the species is clarified and the neotypes of Dolerus asper Zaddach, 1859 and Dolerus brevicornis Zaddach, 1859 are designated. The synonymies of Dolerus asper Zaddach, 1859, to Dolerus planatus Hartig, 1837 and Dolerus derzavini Malaise, 1931, spec. rev. to D. asper Zaddach, 1859 are abandoned. Dolerus carbonarius Zaddach, 1859 and Dolerus fumosus Zaddach, 1859 are considered to be species inquirendae. Phylogenetic analyses of the ITS2 fragment and fragments of ITS2 + COI and ITS2 + COII yielded the topology [D. asper, (D. brevicornis, D. gibbosus)], while those of all other markers and their combinations resulted in the topology [D. brevicornis, (D. asper, D. gibbosus)]. In the latter hypothesis the clade asper + gibbosus is also supported by structural synapomorphies.
The frequently used subspecific name Eleocharis palustris subsp. vulgaris Walters (1949) is a later homonym of E. palustris var. vulgaris Čelak. (1867), so a replacement name, E. palustris subsp. waltersii, is proposed here. Eleocharis palustris var. vulgaris Čelak. is neotypified here with a modern specimen with 2n = 38, making it a taxonomic synonym of E. palustris subsp. waltersii or E. vulgaris “(Walters) Á. Löve et D. Löve”.
Eudiplozoon nipponicum (Goto, 1891) Khotenovsky, 1985 (Monogenea: Diplozoidae), is known to parasitise Cyprinus carpio Linnaeus and species of Carassius. In this study, we conducted a taxonomic re-examination of E. nipponicum using genetic analysis and morphological comparisons from different host species from a single water system. rDNA nucleotide sequences of the internal transcription spacer 2 (ITS-2) region (645 bp) showed interspecific-level genetic differences among diplozoids from species of Carassius and C. carpio (p-distance: 3.1-4.0%) but no difference among those from different species of Carassius (0-0.4%) or between those from C. carpio collected in Asia and Europe (0-1.1%). Large variation was observed among 346 bp cytochrome c oxidase subunit I (COI) sequences (0.3-16.0 %); the topology of the phylogenetic tree showed no relationship to host genera or geographical regions of origin. Morphological observation showed that average clamp size of diplozoids from C. carpio was larger than those from Carassius spp. The number of folds on the hindbody was 10-25 for diplozoids from C. carpio and 12-19 for those from Carassius spp. Thus, our ITS-2 sequence and morphological comparison results indicate that diplozoids from C. carpio and species of Carassius belong to different species. The scientific name E. nipponicum should be applied to the species infected to the type host, Carassius sp. of Nakabo (2013) (Japanese name ginbuna). The diplozoid infecting C. carpio (Eurasian type) should be established as a new species: Eudiplozoon kamegaii sp. n. A neotype of E. nipponicum is designated in this report because the original E. nipponicum specimens are thought to have been lost.
Soricinia tripartita Żarnowski, 1955 is redescribed on the basis of specimens from the type host Sorex araneus Linnaeus from Lithuania, Latvia and Russia (Republic of Karelia and Republic of Komi - a new geographical record) as well as from Sorex satunini Ognev and Sorex volnuchini Ognev from Russia (Nalchik Area in the Caucasus Mountains). The strobilar morphology of S. tripartita is compared with that of other hymenolepidid cestodes of shrews with an unarmed scolex and serial development of proglottides in the strobila, i.e. species of Mathevolepis Spassky, 1948, Ditestolepis Soltys, 1952, Spasskylepis Schaldybin, 1964, Ecrinolepis Spassky et Karpenko, 1983 and Diorchilepis Lykova, Gulyaev, Melnikova et Karpenko, 2006. It was noted that S. tripartita does not correspond to any of the known genera. The following unique characters are found for S. tripartita: heteronomous serial strobilation with one or two sterile proglottides at the end of each series in the strobila and the whole copulatory part of the vagina covered with numerous, fine spines. Therefore, the new genus Gulyaevilepis is erected, with Gulyaevilepis tripartita (Żarnowski, 1955) comb. n. as its type and only species. Since the type material of Soricinia tripartita is not known to exist, a neotype from the same host species and from a locality close to the type locality is designated.
A new genus, Ritacestus, is proposed to accommodate Ritacestus ritaii (Verma, 1926) comb. n. (syn. Proteocephalus ritaii), a parasite of the catfish Rita rita (Hamilton) in India. The new genus, which is placed in the Gangesiinae, is characterized by (i) a small, subspherical scolex formed by four large lobes separated from one another by longitudinal grooves, with a large, widely oval to pyriform rostellum-like apical organ, larger than suckers and possessing an apical hemispherical depression; (ii) paramuscular and cortical position of some vitelline follicles (most follicles are situated medullary); (iii) ventral and dorsal bands of vitelline follicles usually uninterrupted ventral to terminal genitalia and reaching to the posterior margin of proglottides; (iv) the vagina always anterior to the cirrus-sac; (v) a large size of the body (length up to 51 cm); and (vi) development of the uterus of type 2. In its morphology, especially shape of the scolex and apical organ, and paramuscular and cortical position of some vitelline follicles, Ritacestus resembles Postgangesia Akhmerov, 1969, but differs in the presence of a genital atrium (both genital pores of Postgangesia are separate), the anterior position of the vagina (almost always posterior in the latter genus), position of vitelline follicles in cross sections (dorsal and ventral bands in Ritacestus versus only a lateral band in the latter genus), and dorsal excretory canals indistinguishable in mature and gravid proglottides of R. ritaii (well developed in Postgangesia spp.). The type and only species of the genus, R. ritaii, is redescribed on the basis of new material from the type host from the Ganges River basin in India and its neotype is designated.
This paper presents a revision of the genus Dyscia Hübner, [1825] (Lepidoptera, Geometridae: Ennominae). Examination of types and additional material for most described taxa has resulted in several new synonyms: Dyscia ilivolans Wehrli, 1953 syn. n. and Dyscia duanjiao Yang, 1978 syn. n. are new synonyms of Dyscia fagaria (Thunberg, 1784); Dyscia karsholti Wiltshire, 1991 syn. n. is a new synonym of Dyscia galactaria Turati, 1934; Dyscia dagestana Wehrli, 1934 syn. n. is a new synonym of Dyscia malatyana Wehrli, 1934, and Dyscia rjabovi Wardikjan, 1957 syn. n. is a new synonym of Dyscia negrama Wehrli, 1953. One taxon, formerly treated as a species is reassigned to subspecific level, Dyscia conspersaria ssp. sultanica Wehrli, 1936 stat. rev. Dyscia innocentaria sicanaria (Oberthür, 1923) stat. n. and Dyscia malatyana senecai Wiltshire, 1990 stat. n. are downgraded to subspecies-level. On subspecies-level, Dyscia distinctaria perdistincta Herbulot, 1957 syn. n. is a new synonym of Dyscia distinctaria (Bang-Haas, 1910), Dyscia fagaria alvarensis Wahlgren, 1913 syn. n., Dyscia fagaria albescens Lempke, 1952 syn. n., Dyscia fagaria fusca Lempke, 1952 syn. n., and Dyscia fagaria postdelineata Lempke, 1952 syn. n. are new synonyms of Dyscia fagaria. Dyscia fagaria psoricaria (Eversmann, 1848) syn. n. is a new synonym of Dyscia fagaria favillacearia (Hübner, [1799]), Dyscia holli duponti Thierry-Mieg, 1910 syn. n. is a new synonym of Dyscia holli (Oberthür, 1910), Dyscia malatyana nachadira Brandt, 1941 syn. n. and Dyscia malatyana theodoraria Warnecke, 1941 syn. n. are new synonyms of Dyscia malatyana albersaria Warnecke, 1940 stat. n., and Dyscia penulataria naevata Wehrli, 1953 syn. n. is a new synonym of Dyscia penulataria (Hübner, [1819]). Lectotypes for 22 taxa and neotypes for three taxa - Geometra conspersaria [Denis & Schiffermüller], 1775, Geometra favillacearia Hübner, [1799], and Geometra emucidaria Hübner, [1813] - are designated. One species is excluded from Dyscia, Thysanopyga serena (Dognin, 1906) comb. n. From a total of 72 previously described taxa, 19 are recognized as species.
Three rheophilic species of the western Palaearctic Barbus with adjacent geographic distributions are recognised in the Danube River basin, each diagnosed by a set of unique mitochondrial DNA alleles. Barbus petenyi Heckel, 1852 from the Eastern and Southern Carpathians and from the Stara Planina Mts is redescribed and a neotype is designated. Barbus carpathicus, new species, is distributed in the Western and Eastern Carpathians. Barbus balcanicus, new species, occurs in the Dinaric and Western Stara Planina Mts. The three species are morphologically similar to each other but B. balcanicus can be distinguished by subtle differences in the snout shape and body and fin colour pattern. As evident from genetic data the name B. cyclolepis waleckii Rolik, 1970 was proposed for the hybrids between B. barbus and B. carpathicus and cannot be used as valid.