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Two novel species of Russula (Russulaceae, Russulales), R. coronaspora Y.Song sp. nov. and R. minor Y.Song sp. nov. belonging to subgenus Russula crown clade, are described based on both morphological and phylogenetic evidence. In morphology, R. coronaspora sp. nov. is mainly characterized by its distinct spores ornamented with sparse, cylindrical and isolated spines, which resemble coronavirus, and gelatinized pileipellis with pileocystidia mostly septate and sometimes branched; R. minor sp. nov. possesses a very small basidiocarp with pileus less than 2.5 cm in diameter., small basidia, easily peeling and gelatinized pileipellis with slender terminal cells and abundant SV+ pileocystidia. Positions of the two new species in both phylogenetic trees based on ITS and 5-locus sequences (nLSU, mtSSU, rpb1, rpb2 and tef1) confirm their distinct taxonomic status.
Two new species of the genus Eponisiella Emeljanov, 1984 are described and illustrated from China (Guizhou and Shandong Provinces). These are E. dafangensis sp. nov. and E. shandongensis sp. nov., giving the genus eight species in total. A key to the species of Eponisiella is provided as well as a map of their geographic distribution, which is briefly discussed.
Comanopa Blocker, 1979 and Gehundra Blocker, 1976 are small and poorly known genera of leafhoppers, previously comprising four and five species, respectively. In this study, two new species are proposed: Comanopa mananciensis sp. nov. from the state of Paraná, Southern Brazil, and Gehundra cristalinensis sp. nov. from the state of Mato Grosso, Centralwestern Brazil. The male of Gehundra sordida (Baker, 1900) is studied by the first time. Detailed descriptions and illustrations of males and females are provided and keys to males of Comanopa and Gehundra are given.
The Smicridea (Smicridea) fasciatella species group occurs from the southwestern USA, throughout Central America, the Greater Antilles islands, and most of South America, except for the Chilean subregion. It is characterized by the phallic apparatus being a simple tube with eversible internal sclerites at the apex. The fasciatella group is composed of 61 species, of which only 11 occur in Brazil, mainly in the Atlantic Forest biome in the southeastern region. In order to reduce the Linnean and Wallacean shortfalls for the Smicridea Brazilian fauna, we diagnose, describe, and illustrate males of six new species in the fasciatella group: Smicridea (Smicridea) blahniki Desiderio, Pes & Hamada sp. nov., S. (Smicridea) brevitruncata Desiderio, Pes & Hamada sp. nov., S. (Smicridea) caaguara Desiderio, Pes & Hamada sp. nov., S. (Smicridea) ipiranga Desiderio, Pes & Hamada sp. nov., S. (Smicridea) jeaneae Desiderio, Pes & Hamada sp. nov., and S. (Smicridea) polyacantha Desiderio, Pes &; Hamada sp. nov. Additionally, we provide distributional data for S. (Smicridea) albosignata Ulmer, 1907, S. (Smicridea) bivittata (Hagen, 1861), S. (Smicridea) erecta Flint, 1974, S. (Smicridea) obliqua Flint, 1974, S. (Smicridea) paranensis Flint, 1983, and S. (Smicridea) sattleri Denning & Sykora, 1968. The number of S. (Smicridea) species in Brazil increases from 21 to 27 and Smicridea is recorded from the states of Acre, Amapá, and Sergipe for the first time.
Simulium (Trichodagmia) Enderlein, 1934 has an unstable classification system. The broader concept of the subgenus includes five species-groups resulting from an extensive history of synonymisations, often outside of a phylogenetic framework. This concept also ignores relationship hypotheses with the Afrotropical subgenera S. (Anasolen) Enderlein, 1930, S. (Freemanellum) Crosskey, 1969, S. (Xenosimulium) Crosskey, 1969, and the Oviedoi species-group, with several Neotropical species of S. (Trichodagmia). We performed a morphological phylogenetic analysis to test the monophyly of S. (Trichodagmia), its species-groups, and their relationship with the above-mentioned subgenera and Oviedoi species-group. We analysed a data matrix with 69 terminal taxa and 62 characters under parsimony implied weights, with a range of concavities (k1–100), finding three categories of k. Our analysis concludes that S. (Trichodagmia) is not monophyletic, since Oviedoi and the Afrotropical subgenera group with its species-groups Tarsatum and Orbitale. Therefore, we propose a new classification for S. (Trichodagmia) by restricting it to the Orbitale species-group, revalidating S. (Hearlea) Vargas et al., 1946, S. (Hemicnetha) Enderlein, 1934, S. (Obuchovia) Rubtsov, 1947 and S. (Shewellomyia) Peterson, 1975, synonymysing S. (Xenosimulium) with S. (Anasolen), and erecting a new subgenus, S. (Disculter) subgen. nov. for Oviedoi. The geographical distribution of the groups involved is discussed.
The genus Miridiba Reitter, 1902, of phytophagous chafers from Asia, is revised based on external morphological and genital (male and female) characters. In this study, a total fifty-eight species of Miridiba were examined, and the genus is redescribed. Male genital characters of Miridiba, especially the morphology of parameres and endophallus, are studied in depth herein. The female genitalia of Miridiba are studied and described in detail for the first time. According to genital characters, nine genital morphotypes, including fifty-four species, are established under the genus Miridiba. Sixty-seven type specimens are studied. Miridiba gressitti (Frey, 1970) comb. nov., Miridiba borneensis (Moser, 1918) comb. nov., Miridiba coxalis (Arrow, 1944) comb. nov., Miridiba rugaticollis (Moser, 1913) comb. nov., Miridiba nigrescens (Moser, 1916) comb. nov., Miridiba scutata (Reitter, 1902) comb. nov., Miridiba ciliatipennis (Moser, 1903) comb. nov. and Miridiba brunneipennis (Moser, 1916) comb. nov. are transferred from Holotrichia. Holotrichia dalatensis Frey, 1970 is transferred to Miridiba as a synonym of Miridiba sinensis (Hope, 1842). Four junior subjective synonyms are proposed: Miridiba pilosella (Moser, 1908) (= Holotrichia formosana Moser, 1909), Miridiba sinensis (= Holotrichia dalatensis Frey, 1970), Miridiba scutata (= Holotrichia scutulata Dalla Torre, 1912 and Miridiba lassallei Keith, 2010). Miridiba frontalis (Fairmaire, 1886) is resurrected as a valid species. A key to 51 of the 58 valid species of Miridiba is presented.
The present study redescribes four species of Neanthes Kinberg, 1865 (Nereididae de Blainville, 1818) based on their type specimens collected from different worldwide localities: Neanthes chilkaensis (Southern, 1921) from India, N. galetae (Fauchald, 1977) from Panama, N. helenae (Kinberg, 1865) from St Helena Island, and N. mossambica (Day, 1957) from Mozambique. The morphology of the types was re-examined for the first time after the species were originally described, and incorporated the recent improvements in the standards and terminology for describing nereidid features. The arrangement of paragnaths on area VI stood out among the diagnostic features used to distinguish these four species. Neanthes chilkaensis and N. helenae are the unique nereidids bearing p-bar paragnaths on the area VI. Both species are also distinctive as the former species only exhibited p-bar paragnaths on the area VII–VIII and the latter ventrolateral projections on the apodous segment. Further examination revealed that N. nanciae (Day, 1949) from St Helena is a junior synonym of N. helenae. Moreover, N. galetae and N. mossambica are distinguishable from other species also by the development of dorsal cirri, neuropodial postchaetal lobe and ventral ligule, the presence/absence of merged paragnaths on area IV, paired oesophageal caeca, among other features. This study has further contributed to the morphological delimitation of the species in Neanthes as a first step towards revising the genus.
Allomyia renoa (Milne, 1935) (Trichoptera: Apataniidae) was described from six females. The male association is verified in this paper. The original type locality information is limited: “Reno, Nev.,‘78, Morrison”. An Allomyia Banks population found at Mount Rose in Washoe County, Nevada, was compared to the A. renoa type material and found to be the conspecific. Figures, descriptions and distribution of male, female, pupal and larval A. renoa are provided.
In the Pacific Ocean, the taxonomy of the family Zosimeidae Seifried, 2003 is poorly understood and to date only five species of the genus Zosime Boeck, 1873 are known. During oceanographic cruises exploring the species diversity of harpacticoids, two undescribed zosimeid copepods were sampled from shallow Korean waters and the deep northwestern Pacific. A detailed morphological examination has led us to propose two new genera, Heterozosime gen. nov. for the Korean zosimeid H. tenuis gen. et sp. nov. and Acritozosime gen. nov. for the deep-sea zosimeid A. spinesco gen. et sp. nov. Both new genera exhibit a distinctive feature in that the first thoracic leg has a two-segmented exopod, in contrast to the three-segmented exopod of this leg in all known zosimeid genera. Furthermore, Acritozosime gen. nov. can also be discriminated from other genera by the two-segmented endopod in second to fourth thoracic legs and the reduced setal armatures of the second exopodal segment of antenna, the first endopodal segment of first to third thoracic legs and the third exopodal segment in second to fourth thoracic legs. A comparison of the fundamental structures of appendages suggests that A. spinesco gen. et sp. nov. experienced a unique evolutionary history within the Zosimeidae.