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The canaliculatus species group of Stenus (Nestus) is redefined. Four new Palaearctic species of the group are described and illustrated: S. (N.) alopex sp. nov. from the Putorana Highland and Taymyr Peninsula, Russia; S. (N.) canalis sp. nov. from SE Siberia and the Russian Far East; S. (N.) canosus sp. nov. from the Narat Mt Ridge, Chinese Tien Shan; S. (N.) delitor sp. nov. from C & SE Siberia. New distributional data as well as brief analyses of old records for fourteen species described earlier are provided from both Palaearctic and Nearctic material. S. (N.) milleporus Casey, 1884 (= sectilifer Casey, 1884) is revalidated as a species propria. S. (N.) sphaerops Casey, 1884 is redescribed; its aedeagus is figured for the fi rst time; the aedeagus of S. (N.) caseyi Puthz, 1972 as well as aedeagi of eight previously described Palaearctic species are illustrated anew. A key for the identification of all the known Palaearctic species of the group is given. A morphology and ecology based analysis of the main evolutionary trends within the group is provided. A lectotype is designated for S. (N.) melanopus Marsham, 1802; its Siberian and NE European records are supposed to be erroneous; the monotypic melanopus species group is erected.
Morphological and allozyme analyses suggested the occurrence of a pseudocryptic species in the Lasioglossum villosulum (Kirby, 1802) species complex (Hymenoptera: Halictidae). We analysed the morphology of more than 1500 specimens and the DNA barcode fragment of the cytochrome c oxidase subunit I (COI) of 102 specimens of this species complex from several Palaearctic countries. Our phylogenetic tree reconstructions, based on maximum likelihood and Bayesian inference revealed one clade corresponding to all specimens morphologically identified as Lasioglossum medinai (Vachal, 1895) and one divergent specimen morphologically identified as Lasioglossum berberum (Benoist, 1941). The other specimens, morphologically identified as L. villosulum, aggregated into at least three other lineages in our phylogenetic trees. The tree-based species delineations methods based on the Generalized Mixed Yule Coalescent (GMYC) model and the Bayesian Poisson Tree Process (bPTP) identified five to ten candidate species within the L. villosulum species complex, with L. medinai and L. berberum consistently recognized as separated from all other candidate species. Diagnostic morphological differences were found among L. medinai, L. berberum and the remaining specimens identified as L. villosulum. No diagnostic morphological differences were found to distinguish the different phylogenetic candidate species or lineages found within L. villosulum and L. medinai. Thus, both genetic and morphological approaches support the existence of L. medinai and L. berberum as distinct species from L. villosulum.
An update of the current knowledge of Anacharis Dalman, 1823 for the Palaearctic and Indomalayan regions is given. The previously known Palaearctic species Anacharis antennata Belizin, 1951, Anacharis eucharoides (Dalman, 1818), Anacharis immunis Walker, 1835 and Anacharis parapsidalis Belizin, 1951 are redescribed. Three new species are described: Anacharis fergussoni sp. nov. from Europe, Anacharis norvegica sp. nov. from Norway and Anacharis belizini sp. nov. from Thailand, the first recorded Indomalayan species for the genus. Anacharis gracilipes Ionescu, 1969, is synonymized with A. eucharoides, while Anacharis flavidicornis Kieffer, 1910 is transferred to the genus Aegilips Haliday, 1835, resulting in Aegilips flavidicornis (Kieffer, 1910) comb. nov. Diagnostic characters and data about the biology, distribution and affinities with other species of Anacharis are discussed. An identification key for the Palaearctic and Indomalayan species of Anacharis is given.
Representatives of the subgenus Helochares (s. str.) Mulsant, 1844 of China are revised. One new species, H. (s. str.) songi sp. nov., is described from Guangxi, China. All species known from China are redescribed. A diagnosis and a differential diagnosis are provided for each species. Helochares
fuliginosus d’Orchymont, 1932 is recorded for the first time from China and Cambodia. Additional distribution records of H. atropiceus Régimbart, 1903 and H. pallens (MacLeay, 1825) are provided from China. The habitus and aedeagus of all species are illustrated, and a key for the identification of Chinese species of the subgenus is provided.
The Charipinae Dalla Torre & Kieffer, 1910 present in the Palaearctic region are revised; 2410 specimens have been identified, belonging to 75 species: 52 to Alloxysta, one to Apocharips, six to Dilyta and 16 to Phaenoglyphis. For 33 species, new country-level distribution records are provided. Two new species are here described: Alloxysta palearctica Ferrer-Suay & Pujade-Villar sp. nov. and Alloxysta pascuali Ferrer-Suay sp. nov. A diagnosis for these species is included and their diagnostic features are shown in different figures. A key to identify all the species of Charipinae in the Palaearctic region is also given.