Refine
Year of publication
Document Type
- Article (193) (remove)
Language
- English (193) (remove)
Has Fulltext
- yes (193)
Is part of the Bibliography
- no (193) (remove)
Keywords
- new species (193) (remove)
Ten new species of Thinophilus Wahlberg, 1844 from the Afrotropical region are described and illustrated: T. saegeri sp. nov. from the Democratic Republic of the Congo, T. medvedevi sp. nov., T. longicercus sp. nov., T. cataractae sp. nov. and T. manambato sp. nov. from Madagascar, T. gallagheri sp. nov. and T. deemingi sp. nov. from Oman, T. sigwalti sp. nov. from Senegal, T. subpalpatus sp. nov. from South Africa, and T. fluvialis sp. nov. from Tanzania. Type material for 13 previously described Afrotropical species is examined. The genus Paralleloneurum Becker, 1902 is newly synonymized with Thinophilus (syn. nov.). As a result, the following new combinations are here established: Thinophilus cilifemoratus (Becker, 1902) comb. nov. and T. pygmaeus (De Meijere, 1916), comb. nov. The following new synonyms are proposed: Thinophilus annulitarsis Parent, 1936 with T. calopus Loew 1852; T. bipunctatus Curran, 1926 and T. maculatus Parent, 1929 with T. indigenus Becker, 1902. New records are given for some known species. Thinophilus argyropalpis Becker, 1910 and T. spinitarsis Becker, 1907 are reported from the Afrotropical Region for the first time. The number of species of the genus, known from continental Africa, Oman, Yemen and Madagascar, has increased to 30. An identification key to 29 Afrotropical species is compiled. Thinophilus versutus Haliday, 1851 and T. cilifemoratus (Becker, 1902), type species of the former genera Schoenophilus Mik, 1878 and Paralleloneurum Becker, 1902, are subsequently also included into the key, because the two species inhabit northern Africa.
An extensive survey of Linyphiidae spiders from Wulipo National Nature Reserve (NNR), Chongqing has been conducted, in which 24 species belonging to 16 genera are recorded including two new genera and eight new species described here as: Agyneta Hull, 1911, A. orthogonia sp. nov. (♂♀); Dicristatus gen. nov., D. minutus gen. et sp. nov. (♂♀); Dicymbium Menge, 1868, D. pingqianense sp. nov. (♂♀); Himalaphantes Tanasevitch, 1992, H. azumiensis (Oi, 1979) (♂♀); Indophantes Saaristo & Tanasevitch, 2003, I. wushanensis sp. nov. (♂♀); Ketambea Millidge & Russell-Smith, 1992, K. nigripectoris (Oi, 1960) (♂♀); Molestia Tu, Saaristo & Li, 2006, M. pollicaris sp. nov. (♂♀); Neriene Blackwall, 1833, N. calozonata Chen & Zhu, 1989 (♀), N. cavaleriei (Schenkel, 1963) (♂♀), N. emphana (Walckenaer, 1841) (♂♀), N. japonica (Oi, 1960) (♂♀), N. limbatinella (Bösenberg & Strand, 1906) (♀), N. longipedella (Bösenberg & Strand, 1906) (♂♀), N. oidedicata van Helsdingen, 1969 (♀); Prosoponoides Millidge & Russell-Smith, 1992, P. sinense (Chen, 1991) (♂♀); Ryojius Saito & Ono, 2001, R. simplex sp. nov. (♂♀); Stemonyphantes Menge, 1866, S. bifurcus sp. nov. (♂); Syedra Simon, 1884, S. oii Saito, 1983; Tapinopa Westring, 1851, T. guttata Komatsu, 1937 (♀); Tenuiphantes Saaristo & Tanasevitch, 1996, T. ancatus (Zhu, Li & Sha, 1986) (♂♀); Walckenaeria Blackwall, 1833, Walckenaeria asymmetrica Song & Li, 2011 (♂♀); Wuliphantes gen. nov., W. guanshan (Irfan, Wang & Zhang, 2022) gen. et comb. nov. (♂♀), W. tongluensis (Chen & Song, 1988) gen. et comb. nov. (♂♀), W. trigyrus gen. et sp. nov. (♂♀). Male of Tenuiphantes ancatus (Zhu, Li & Sha, 1986) is described here for the first time as new to science. The taxonomic status of Bathyphantes guanshan Irfan, Wang & Zhang, 2022 and Bathyphantes tongluensis (Chen & Song, 1988) is revised and proposed here as: Wuliphantes tongluensis (Chen& Song, 1988) gen. et comb. nov. (♂♀) and Wuliphantes guanshan (Irfan, Wang & Zhang, 2022) gen. et comb. nov. (♂♀), respectively. Morphological descriptions, photos of body and copulatory organs, as well as the locality map are provided.
Bujurquina is the most widely distributed and species-rich genus of cichlids in the western Amazon of South America. In this study we describe a new species from Peru from a hypothesized reverse flowing river system. Prior to the origin of the modern Amazon River at 4.5 Ma, this river system had its headwaters on the Iquitos arch, one of several main structural arches (swells) in the Amazon. Prior to the origin of the modern Amazon these arches formed topographic barriers of drainage basins in lowland Amazonia. For our analyses we use morphological and molecular data, analyzed through multivariate statistics and molecular phylogenies, respectivelly. For all valid species in the genus (except B. cordemadi and B. pardus) we additionally for the first time provide photographs of live specimens. Based on DNA phylogeny and coloration patterns we demonstrate that Bujurquina is divided into two main clades and based on this we provide a dichotomous key for all the species.
Inocybe hopeae sp. nov. and first record of Pseudosperma keralense (Inocybaceae) from Thailand
(2023)
Based on genetic studies, supported further by morphological and ecological differences, we present a taxonomic novelty (Inocybe hopeae Raghoonundon & Raspé sp. nov.) and a new geographical record (Pseudosperma keralense) from forests of Northern Thailand. Inocybe hopeae is characterized by medium-sized basidiomes, brownish orange to brown pileus that is darker towards the margin, off-white to pale brown context, light brown to dark brown stipe with off-white basal mycelium and pale brown to grayish brown lamellae. A three-gene phylogeny (LSU, tef1, rpb2) coupled with macroscopic / microscopic descriptions and illustrations are provided confirming the species’ positions in their respective generic clades. Inocybe hopeae was sister to I. thailandica with strong support (BS = 100%, PP = 1.0). Our Thai collections of OR1629 had similar morphological characters and 100% identical sequences with the holotype of Pseudosperma keralense from India.
In order to provide a reassessment of the Neotropical genus Pseudonannolene Silvestri, 1895, a cladistic analysis, biogeographic analysis, and taxonomic review were conducted in the present work. For the cladistic approach, 91 morphological characters were scored for 53 terminals as the ingroup and 10 as the outgroup. Three synapomorphies support the monophyly of the genus: presence of a longitudinal suture on the promentum, penial bases partially fused, and the internal branch of the gonopods surrounding the telopodite; and two homoplastic transformations: the lateral lobe of the collum densely striated and setae present up to the apical portion of the prefemoral process on the first leg-pair of males. The genus Pseudonannolene is recovered as sister-group of Epinannolene Brölemann, 1903 (Pseudonannoleninae). A total of 226 occurrence points were recorded for Pseudonannolene, with the majority of records from the Chacoan subregion, composed by Araucaria Forest, Atlantic, and Parana Forest provinces. The biogeographical searches using the Geographically explicit Event Model recovered two biogeographic reconstructions (cost of 79 000), with the vicariance events occurring more frequently in the deep clades, whereas sympatry and points of sympatry occurred in more inclusive clades. The first reconstruction recovered four vicariances, 13 sympatries, 4 points of sympatry, and 21 founder events, and the second reconstruction recovered four vicariances, 12–13 sympatries, 4–5 points of sympatry, and 21 founder events. The genus Pseudonannolene comprises 56 species, including 8 new species herein described: P. alata sp. nov., P. aurea sp. nov., P. bucculenta sp. nov., P. curvata sp. nov., P. granulata sp. nov., P. insularis sp. nov., P. morettii sp. nov., and P. nicolau sp. nov.; P. brevis Silvestri, 1902 and P. rugosetta Silvestri, 1897 are regarded as species inquirendae; a neotype of P. alegrensis Silvestri, 1897 is here proposed with male described for the first time. The following taxa are synonymized: P. canastra Gallo & Bichuette, 2020 and P. saguassu Iniesta & Ferreira, 2013 with P. ambuatinga Iniesta & Ferreira, 2013; P. marconii Iniesta & Ferreira, 2013 with P. longicornis (Porat, 1888); P. chaimowiczi Fontanetti, 1996, P. gogo Iniesta & Ferreira, 2013, P. rosineii Iniesta & Ferreira, 2014, P. taboa Iniesta & Ferreira, 2014, and P. longissima Iniesta & Ferreira, 2014 with P. microzoporus Mauriès, 1987; P. tricolor gracilis Brölemann, 1902 and P. tricolor rugosus Schubart, 1945 with P. tricolor Brölemann, 1902; P. auguralis Silvestri, 1902 with P. rocana Silvestri, 1902; and P. abbreviata Silvestri, 1902 with P. typica Silvestri, 1895. P. inops Brölemann, 1929 is proposed here as new status from P. bovei inops. A dichotomous identification key is presented to facilitate the species identification.
Three novel species collected from Dinghushan Biosphere Reserve (DHSBR) in southern China, Russula cylindrica Y.Song sp. nov. and R. lacteocarpa Y.Song sp. nov. in subgenus Archaeae and R. reticulofolia Y.Song sp. nov. in subg. Compactae, are described based on morphological and molecular data. In addition, Russula leucobrunnea Y.Song nom. nov. is proposed in replacement of R. leucocarpa nom. illeg. in subg. Brevipedum, as R. leucocarpa (T.Lebel) T.Lebel had been described earlier. Differences between the three novel species and their closely related taxa were analyzed. Another two known species in subg. Brevipedum, R. callainomarginis J.F.Liang & J.Song and R. japonica Hongo were also identified among specimens from DHSBR and are described and illustrated. Phylogenetic analyses of ITS and a five-locus phylogeny (concatenated LSU, mtSSU, rpb1, rpb2 and tef1) support the recognition of these taxa.
The justification of the 4 genera that currently compose the class Pavlovophyceae is based on a low number of species and a relative paucity of available, traceable and referenced cultures. Previous integrative phylogeny work revealed strains that can refine and strengthen our knowledge of the genera in the class. The application of multiple light and electron microscopy techniques allowed us to prioritize the cytomorphological characters (pyrenoid, thylakoid, stigma, knob-scales, life stage / life cycle) used for the taxonomy of these algae and to describe two new species: Exanthemachrysis fresneliae Véron sp. nov. and Rebecca billardiae Véron sp. nov. Consequently, revisions of the two genera Exanthemachrysis Lepailleur emend. Véron and Rebecca Green emend. Véron were made. In addition, the genus Pavlova Butcher emend Véron is revised in the light of these characters. Particular emphasis is placed on the life stages and habitat of the species.
Based on morphological and molecular evidence, two new species of Silene are recognized and described here, S. penduliflora F.Jafari, Keshavarzi & Doostm. sp. nov. and S. thyrsiantha F.Jafari, Mirtadz. & Keshavarzi sp. nov. The newly discovered species are distributed in the central and southeastern parts of Iran, growing in rocky habitats. Relationships among these species and their close relatives are demonstrated using nrDNA ITS and cpDNA rps16 phylogenies. Silene ghahremaninejadii, S. parrowiana, and S. shahrudensis form a clade with these new species. A key to S. penduliflora and S. thyrsiantha and their close relatives is provided.
The Lasioglossum (Dialictus) gemmatum species complex, also known as the L. tegulare species group and the L. parvum species complex, is a very common, widespread, diverse, and recognisable lineage of sweat bees, containing 22 previously described species and several known undescribed species. The species were recently revised for the eastern Nearctic region and the Greater Antilles, but remain poorly known in the western Nearctic along with most other L. (Dialictus). These characteristics make it a prime candidate for revision in ongoing taxonomic work on the western Nearctic L. (Dialictus). Here we present the results of this revision, including 10 new species descriptions, one new synonymy, a preliminary phylogeny, and keys to known Nearctic species. Species of the eastern Nearctic and a few primarily Neotropical species which can occur in the Nearctic are also included. We report that the L. (D.) gemmatum species complex is likely a monophyletic group arising from the L. (D.) comulum group, but that the enlarged tegula has arisen independently in at least two other L. (Dialictus) lineages, and it contains multiple cases of allopatric speciation. The following species are described as new: Lasioglossum (Dialictus) angelicum sp. nov., L. (D.) deludens sp. nov., L. (D.) diabolicum sp. nov., L. (D.) eremum sp. nov., L. (D.) gloriosum sp. nov., L. (D.) indagator sp. nov., L. (D.) holzenthali sp. nov., L. (D.) magnitegula sp. nov., L. (D.) profundum sp. nov., and L. (D.) rufodeludens sp. nov. Previously undescribed males of L. (D.) perparvum (Ellis, 1914) and L. (D.) pseudotegulare (Cockerell, 1896) and the female of L. (D.) gaudiale (Sandhouse, 1924) are diagnosed and figured for the first time. Lasioglossum (Dialictus) hunteri (Crawford, 1932) is a new subjective junior synonym of L. (D.) ellisiae (Sandhouse, 1924). Pre-2022 specimen records of L. (D.) hunteri and L. (D.) tegulariforme (Crawford, 1907) are attributable to a heterogeneous mix of species, and records of L. (D.) perparvum are likely attributable to L. (D.) deludens.
Six new and four known species of the genus Axonchium Cobb, 1920 are described and illustrated from the Western Ghats of India. Axonchium indicum sp. nov. has a 1.2–1.4 mm long body, offset lip region, 8–9 µm long odontostyle, expanded part of pharynx 39–49 % of total neck length, anterior uterine sac 0.9–1.6 times the mid-body diameter long, and a bluntly conoid tail. Axonchium microspiculum sp. nov. has a 1.1–1.22 mm long body, offset lip region, 7–8 µm long odontostyle, 20–23 µm long spicules, two weakly developed ventromedian supplements, and obtusely rounded tail. Axonchium nilgiriense sp. nov. has a 1.4–1.6 mm long body, offset lip region, 8–9 µm long odontostyle, vagina strongly bent posteriad, 37–41 µm long spicules, 3–4 ventromedian supplements, and bluntly conoid tail. Axonchium paracingulatum sp. nov. has a 2.5–2.8 mm long body, offset lip region, 10–11 µm long odontostyle, vaginal lumen highly expanded in the middle, 69 µm long spicules, and broadly conoid tail with rounded terminus. Axonchium tropicum sp. nov. has a 1.7–2.0 mm long body, offset lip region, 11–12 µm long odontostyle, anterior uterine sac 2.3–4.0 times the mid-body diameter long, 40 µm long spicules, 4 widely spaced ventromedian supplements, and broadly rounded tail. Axonchium uniqum sp. nov. has a 1.7–2.0 mm long body, offset lip region, 10–11 µm long odontostyle, anterior uterine sac 2.5–2.8 times mid-body diameter long, 68 µm long and slender spicules, and broadly conoid tail. Axonchium nitidum, A. saccatum, A. transkeiense and A. vallum are redescribed based on specimens collected from several localities. A diagnostic key to the identification of the valid species of this genus is provided.