Refine
Year of publication
- 2022 (6) (remove)
Document Type
- Article (6)
Language
- English (6)
Has Fulltext
- yes (6)
Is part of the Bibliography
- no (6) (remove)
Keywords
- systematics (6) (remove)
Acrostilicus Hubbard, 1896 and Pachystilicus Casey, 1905 are North American genera known from only one and two species, respectively, and have never been a subject of a modern revision. In fact, Acrostilicus was not even properly described as its author provided only a sketchy diagnosis of the genus and species. Here, we provide a redescription of the genus Acrostilicus and its species and illustrate the habitus and male genital features. For the first time, we also redescribe Pachystilicus and its two species, and provide their differential diagnoses. Additionally, we tested the phylogenetic position of both genera. They were scored into a morphological matrix supplemented with molecular data and the analyses were run using Bayesian inference and maximum likelihood methods. A total of 119 morphological characters and 4859 bp of nuclear (28S, TP, Wg, CADA, CADC, ArgK) and mitochondrial (COI) sequences were analysed for 46 taxa. The results confirmed that both Acrostilicus and Pachystilicus are members of the subtribe Stilicina, but at the same time challenged the monophyly of the subtribe in its current composition. Additionally, we provided further evidence for non-monophyly of the subtribe Medonina and discussed the biology of Acrostilicus and Pachystilicus.
This paper contains the results of research on a large assemblage of jumping spiders collected by J.-C. Ledoux from Ivory Coast in 1974–75. In total, 105 species are included. Three new genera are erected Pulcherula gen. nov., Sphericula gen. nov. and Vicirionessa gen. nov. Two generic names are synonymized, Polemus Simon, 1902 with Baryphas Simon, 1902 and Brancus Simon, 1902 with Thyene Simon, 1885. Twenty eight new species are described: Afraflacilla albopunctata sp. nov. (♀), Ansienulina lamottei sp. nov. (♂), Asemonaea pusilla sp. nov. (♀), Detalik cavally sp. nov. (♀), Evarcha zougoussi sp. nov. (♀), Heliophanus (Heliophanus) minimus sp. nov. (♂♀), Hyllus ignotus sp. nov. (♀), Hyllus solus sp. nov. (♀), Hyllus unicolor sp. nov. (♀), Icius bandama sp. nov. (♂♀), Langona recta sp. nov. (♂), Malizna zabkai sp. nov. (♀), Menemerus niangbo sp. nov. (♀), Myrmarachne galea sp. nov. (♀), Phintella brevis sp. nov. (♂), Phintella globosa sp. nov. (♀), Phintella occidentalis sp. nov. (♂), Phintella transversa sp. nov. (♂), Pochytoides mirabilis sp. nov. (♂♀), Pochytoides tonkoui sp. nov. (♀), Pochytoides tournieri sp. nov. (♂), Pulcherula magna gen. et sp. nov. (♂), Rhene ferkensis sp. nov. (♀), Sonoita ledouxi sp. nov. (♂♀), Sphericula globulifera gen. et sp. nov. (♀), Thiratoscirtus silvestris sp. nov. (♂♀), Tusitala bandama sp. nov. (♀) and Tusitala cornuta sp. nov. (♂). Five specific names are synonymized: Polemus chrysochirus Simon, 1902 with Baryphas jullieni Simon, 1902, Viciria mondoni Berland & Millot, 1941with Malloneta guineensis Simon, 1902, Brancus lacrimosus Wesołowska & Edwards 2008 with Vicirionessa fuscimana (Simon, 1903), Viciria monodi Berland & Millot, 1941 and Viciria equestris pallida Berland & Millot, 1941 with Vicirionessa equestris (Simon, 1903). Hyllus natali peckhamorum Berland & Millot, 1941 is removed from synonymy of Hyllus brevitarsis Simon, 1902, revalidated and its rank is raised as Hyllus peckhamorum Berland & Millot, 1941 stat. nov. Also rank of Telamonia aequipes minor Lessert, 1925 is elevated as Phintella minor (Lessert, 1925) stat. nov. Menemerus dubius Berland & Millot, 1941 is removed from nomina dubia. This species is considered valid and is redescribed. A lectotype is designated for it. The male of Mexcala torquata Wesołowska, 2009 and females of Hyllus tuberculatus Wanless & Clark, 1975, Iranattus principalis (Wesołowska, 2000), Myrmarachne eidmanni Roewer, 1942 and Thiratoscirtus tentativus (Szűts & Jocqué, 2001) are described for the first time. Many new combinations are proposed. Twenty ex Brancus are recombined: Hyllus nigeriensis (Wesołowska & Edwards, 2012) comb. nov., Thyene blaisei (Simon, 1902) comb. nov., Thyene calebi (Kanesharatnam & Benjamin, 2018) comb. nov., Thyene mutica (Simon, 1902) comb. nov., Thyene verdieri (Berland & Millot, 1941) comb. nov., Vicirionessa besanconi (Berland & Millot, 1941) gen. et comb. nov., Vicirionessa fuscimana (Simon, 1903) gen. et comb. nov., Vicirionessa mustela (Simon, 1902) gen. et comb. nov., Vicirionessa niveimana (Simon, 1902) gen. et comb. nov., Vicirionessa occidentalis (Wesołowska & Russell-Smith, 2011) gen. et comb. nov., Vicirionessa peckhamorum (Lessert, 1927) gen. et comb. nov., Vicirionessa signata (Dawidowicz & Wesołowska, 2016) gen. et comb. nov. Four ex Viciria are recombined: Vicirionessa chabanaudi (Fage, 1923) gen. et comb. nov., Vicirionessa equestris (Simon, 1903) gen. et comb. nov., Vicirionessa prenanti (Berland & Millot, 1941) gen. et comb. nov., Vicirionessa tergina (Simon, 1903) gen. et comb. nov. and one species ex Hyllus: Vicirionessa albocincta (Thorell, 1899) gen. et comb. nov. Furthermore, the following two new combinations are proposed: Thiratoscirtus tentativus (Szűts & Jocqué, 2001) comb. nov. (ex Bacelarella) and Baryphas galeatus (Simon, 1902) comb. nov. (ex Polemus). For 11 species known so far from single records new data are presented: Heliophanus butemboensis Wesołowska, 1986, Hyllus lwoffi Berland & Millot, 1941, Hyllus tuberculatus Wanless & Clark, 1975, Menemerus dubius Berland & Millot, 1941, Mexcala torquata Wesołowska, 2009, Neaetha maxima Wesołowska & Russell-Smith, 2011, Pachyballus miniscutulus Wesołowska, Azarkina & Wiśniewski 2020, Phintella paludosa Wesołowska & Edwards, 2012, Thiratoscirtus gambari Wesołowska & Russell-Smith, 2011, Tusitala guineensis Berland & Millot, 1941 and Tusitala lutzi Lessert, 1927.
We describe two new species of Cyrtodactylus Gray, 1827, each from the Indian states of Meghalaya and Mizoram based on morphology and ND2 gene sequences. The new species are a part of the Cyrtodactylus khasiensis group. Both species represent the highland clade within the south of Brahmaputra clade of Indo-Burmese Cyrtodactylus. Based on ND2 gene sequence, the species from Meghalaya have an uncorrected p-distance of 4.21%–4.25% from a lowland species C. guwahatiensis Agarwal, Mahony, Giri, Chaitanya & Bauer, 2018 and is a sister taxon to C. septentrionalis Agarwal, Mahony, Giri, Chaitanya & Bauer, 2018. The species from Mizoram differ from its sister species C. bengkhuaiai Purkayastha, Lalremsanga, Bohra, Biakzuala, Decemson, Muansanga, Vabeiryureilai, Chauhan & Rathee, 2021 by a p-distance of 8.33%.
The genera Aneflomorpha Casey, 1912 and Neaneflus Linsley, 1957 (Coleoptera: Cerambycidae) are revised for the species occurring in the United States. Examination of all primary types has necessitated redefinition of several species that were defined originally and subsequently on erroneous character descriptions. Two new species of Aneflomorpha are described from Arizona: Aneflomorpha crypta Lingafelter, new species and A. paralinearis Lingafelter new species. One subspecies, Aneflomorpha rectilinea yumae Giesbert and Hovore, 1976 is elevated to species, new status. Six species are synonymized: Aneflomorpha citrana Chemsak, 1960 is a new synonym of A. rectilinea Casey, 1924; Aneflomorpha parowana Casey, 1924 is a new synonym of Aneflomorpha linearis (LeConte 1859), along with its synonyms A. testacea Casey, 1924, A. elongata Linsley, 1936, and A. californica Linsley, 1936; Aneflomorpha arizonica Linsley, 1936 is a new synonym of Aneflomorpha unispinosa Casey, 1912; Aneflomorpha parkeri Knull, 1934 is a new synonym of Aneflomorpha gilana Casey, 1924; Aneflomorpha texana Linsley 1936 is removed from synonymy with A. seminuda Casey, 1912 and found to be conspecific with A. werneri Chemsak, 1962, new synonym. Aneflomorpha opacicornis Linsley, 1957 is transferred to Neaneflus as N. opacicornis (Linsley), new combination, and Neaneflus brevispinus Chemsak, 1962 is a new synonym. With this revision, there are eighteen species of Aneflomorpha and two species of Neaneflus recognized for the United States. All species are presented with new diagnoses, illustrated characters, updated distributional and host information, and an illustrated identification key.
ZooBank registration. urn:lsid:zoobank.org:pub:08BF4EE0-E69C-4E09-BECA-26481D49BFDE
Four new species of limnoterrestrial rhabdocoels (‘Typhloplanidae’ Graff, 1905) are described. One of these – Faunulus nielsi Houben, Proesmans & Artois gen. et sp. nov. – could not be unambiguously placed within an existing genus. Faunulus nielsi most closely resembles species of the genus Adenocerca Reisinger, 1924 but can be clearly distinguished by the position of the testes. The three other new species described are Bryoplana belgica Houben, Proesmans & Artois sp. nov., Hoplopera isis Houben, Proesmans & Artois sp. nov., and Protoplanella leiae Houben, Proesmans & Artois sp. nov. All three belong to the subfamily ‘Protoplanellinae’ Reisinger, 1924 and are distinguished based on a detailed description of the reproductive system. Finally, new data are provided for nine other, known typhloplanids: Adenocerca minima Kolasa, 1981; Chorizogynopora italica Kolasa, 1981; Hoplopera opaca Reisinger, 1924; K. subterranea Reisinger, 1933; Krumbachia virginiana (Kepner & Carter, 1931) Ruebush, 1938; Olisthanellinella rotundula Reisinger, 1924; Prorhynchella minuta Ruebush, 1939; Protoplanella simplex Reisinger, 1924; and Ventrociliella romanae Kolasa, 1977. A detailed comparison of our material of V. romanae to what is described for Bockia deses Reisinger, 1924, leads us to consider the latter a nomen dubium.
The New Zealand alpine cave wētā genus Pharmacus was first described by Pictet & de Saussure (1893) as a monotypic taxon. Three species were added to the genus by Richards in 1972. Here we clarify the status and appearance of all known species of Pharmacus. Based on morphology and mtDNA sequences we determine that the species Pharmacus brewsterensis Richards, 1972 is better placed within the genus Notoplectron Richards, 1964. We also resolve the species Isoplectron cochleatum Karny, 1935 and show that it belongs to the genus Pharmacus. Additionally, we describe six new species and three new subspecies from the southern regions of South Island, New Zealand. We provide key traits and known distributions for all known species and subspecies in this alpine genus. New combinations: Pharmacus brewsterensis Richards, 1972 becomes Notoplectron brewsterense (Richards, 1972) comb. nov.; Isoplectron cochleatum Karny, 1935 becomes Pharmacus cochleatus (Karny, 1935) comb. nov. New species and subspecies: Pharmacus cochleatus rawhiti subsp. nov., Pharmacus cochleatus fiordensis subsp. nov., Pharmacus cochleatus nauclerus subsp. nov., Pharmacus concinnus sp. nov., Pharmacus cristatus sp. nov., Pharmacus notabilis sp. nov., Pharmacus perfidus sp. nov., Pharmacus senex sp. nov. and Pharmacus vallestris sp. nov. New synonyms: Pharmacus dumbletoni Richards, 1972 = Pharmacus montanus Pictet & de Saussure, 1893 syn. nov.; Pharmacus chapmanae Richards, 1972 = Pharmacus cochleatus (Karny, 1935) syn. nov.