Refine
Year of publication
- 2012 (11) (remove)
Document Type
- Part of Periodical (8)
- Article (3)
Language
- English (11)
Has Fulltext
- yes (11) (remove)
Is part of the Bibliography
- no (11)
Keywords
- taxonomy (11) (remove)
The lichen-forming genus Pertusaria under its current circumscription is polyphyletic and its phylogenetic affiliations are uncertain. Here we study the species of the genera Pertusaria and Varicellaria which containlecanoric acid as major constituent, have disciform apothecia, strongly amyloid asci, non-amyloid hymenial gel, 1-2-spored asci, and 1- or 2-celled ascospores with thick, 1-layered walls. We infer phylogenetic relationships using maximum likelihood and Bayesian analyses based on four molecular loci (mtSSU, nuLSU rDNA, and the protein-coding, nuclear RPB1 and MCM7 genes). Our results show that the lecanoric acid-containing species form a well-supported, monophyletic group, which is only distantly related to Pertusaria s.str. The phylogenetic position of this clade is unclear, but placement in Pertusaria s.str. is rejected using alternative hypothesis testing. The circumscription of the genus Varicellaria is enlarged to also include species with non-septate ascospores. Seven species are accepted in the genus: Varicellaria culbersonii (Vězda) Schmitt & Lumbsch, comb. nov., Varicellaria hemisphaerica (Flörke) Schmitt & Lumbsch, comb. nov., Varicellaria kasandjeffii (Szatala) Schmitt & Lumbsch, comb. nov., Varicellaria lactea (L.) Schmitt & Lumbsch, comb. nov., Varicellaria philippina (Vain.) Schmitt & Lumbsch, comb. nov., Varicellaria rhodocarpa (Körb.) Th. Fr., and Varicellaria velata (Turner) Schmitt & Lumbsch, comb. nov. A key to the species of Varicellaria is provided.
Results of the odonatological survey of the coastal SW regions of Cambodia in August 12-28, 2011 are presented. Those include general notes on the Odonata fauna in late rainy season, enumeration of all records by locality, discussion of interesting specimens and their taxonomy, and notes on habitats and habits of some species. Of 87 named Odonata species encountered during the trip, 15 are reported for the first time for Cambodia, namely Aciagrion hisopa (Selys, 1876), Anax immaculifrons Rambur, 1842, Burmagomphus divaricatus Lieftinck, 1964, Gomphidictinus perakensis (Laidlaw, 1902), Merogomphus parvus (Kruger, 1899), Nepogomphus walli (Fraser, 1924), Idionyx thailandica Hamalainen, 1985, Macromia cupricincta Fraser, 1024, Macromia septima Martin, 1904, Macromidia rapida Martin, 1907, Agrionoptera insignis (Rambur, 1842), Lyriothemis elegantissima Selys, 1883, Onychothemis testacea Laidlaw, 1902, Orthetrum luzonicum (Brauer, 1868), Orthetrum testaceum (Burmeister, 1839). The country list now reaches 125 named species.
The South African endemic bee genus Redivivoides Michener, 1981 is revised and redefined. The genus comprises seven species, six of which are described here as new: Redivivoides capensis sp. nov. ♀♂, R. eardleyi sp. nov. ♀, R. kamieskroonensis sp. nov. ♀, R. karooensis sp. nov. ♀♂, R. namaquaensis sp. nov. ♀♂ and R. variabilis sp. nov. ♀♂. A key to species is provided.
The genus Candobrasilopsis gen. nov. is here described, with C. rochai gen. nov. sp. nov. as type species, from the alluvial valley of the Upper Paraná River. The enigmatic Candonopsis brasiliensis Sars, 1901 is here redescribed and transferred to this new genus, the new combination being Candobrasilopsis brasiliensis (Sars, 1901). The new candonid genus belongs to the tribe Candonopsini, because of the absence of the proximal seta on the caudal ramus. It is closely related to Latinopsis Karanovic & Datry, 2009, because of the relatively short terminal segment of the mandibular palp (length less than 1.5 times the basal width, while this segment is longer than three times the basal width in Candonopsis) and the large and stout b-seta on the T1. However, it differs markedly from Latinopsis in the size and shape of the calcified inner lamellae of both valves and in the type of hemipenis. We also discuss the doubtful allocation of several other genera to the Candonopsini, raise Abcandonopsis Karanovic, 2004 to generic status and reassess the uncertain position of Candonopsis anisitsi Daday, 1905 within Latinopsis.
This paper summarizes current knowledge about East African pholcids. East Africa is defined as the area from 12°S to 5°N and from 28° to 42°E, including all of Uganda, Kenya, Burundi, Rwanda, and Tanzania. An annotated list of the 15 genera and 87 species recorded from this area is given, together with distribution maps and an identification key to genera. Most East African species (90%) belong to one of only six genera: Buitinga Huber, 2003 (21 species); Smeringopus Simon, 1890 (18); Pholcus Walckenaer, 1805 (17); Spermophora Hentz, 1841 (12); Leptopholcus Simon, 1893 (5) and Quamtana Huber, 2003 (4). Eight species for which DNA sequence data have been published recently are newly described: Buitinga batwa sp. nov., B. wataita sp. nov., Spermophora mau sp. nov., S. maathaiae sp. nov., S. bukusu sp. nov., S. kirinyaga sp. nov., S. kyambura sp. nov. and Quamtana nyahururu sp. nov. Crossopriza johncloudsleyi Deeleman-Reinhold & van Harten, 2001, previously only known from Yemen, is redescribed based on specimens from Kenya. Additional new records are given for 21 previously described species.
Capalictus, a new subgenus of Lasioglossum Curtis, 1833 (Hymenoptera, Apoidea, Halictidae), endemic to the South African Cape Province, is described. The type species is Halictus mosselinus Cockerell, 1945. Evylaeus (Sellalictus) fynbosensis (Pauly et al., 2008) is a new junior synonym of L. (C.) mosselinum. Three new species are described: Lasioglossum (Capalictus) hantamense sp. nov., L. (C.) tigrinum sp. nov. and L. (C.) timmermanni sp. nov. DNA sequence data from three nuclear genes support morphologically-determined species limits. Capalictus is a basal clade of the Hemihalictus series of Lasioglossum.
A revision of the known African species of Psammoecus is given, including redescriptions and illustrations of diagnostic characters. Extensive material from the Musée royal de l’Afrique centrale (Tervuren) is studied. Two new species are described: Psammoecus leleupi sp. nov., and Ps. luchti sp. nov. Four specific names are synonymized: Psammoecus excellens Grouvelle, 1908 = Ps. trimaculatus Motschulsky, 1858; Ps. alluaudi Grouvelle, 1912 = Ps. trimaculatus Motschulsky, 1858; Ps. longulus Grouvelle, 1878 = Ps. longicornis Schaufuss, 1872; Ps. nitescens Grouvelle, 1914 = Ps. laetulus Grouvelle, 1914. A key to the African species is provided.
No Name, No Game
(2012)
In an interesting contribution Joppa et al. (2011) revisit some aspects of the taxonomic impediment (Evenhuis 2007; http://www.cbd.int/gti/) and come to the conclusion that, contrary to the generally accepted idea, both the rates of species description and the number of taxonomists have increased exponentially since the 1950’s. Joppa et al. (2011) also note a marked decline in the number of species described per taxonomist which they attribute to the difficulty of finding new species in an ever declining ‘missing species pool’. Therefore, their results might be interpreted that today’s taxonomic workforce is sufficient to describe the remaining (shallow) ‘pool of missing species’. In this contribution, we question if this is indeed the case and propose a solution for speeding up taxonomic descriptions.
Three new species of Helicopsyche Siebold, 1856 are described from Vietnam: Helicopsyche melina sp. nov., Helicopsyche meander sp. nov., and Helicopsyche lamnata sp. nov. All species were described from Melinh Station for Biodiversity in the Me Linh District of Vinh Phuc Province. The species were collected mainly in Malaise traps situated across a small stream surrounded by lowland forest. Some individuals were also collected on light in traps situated at the stream bank.
Three different male and female super-specific types are distinguished according to variations in the morphology of the bulb and spermathecae within the genus Nemesia Audouin, 1826. Plotting the distributions of these sexual types on a map of the Mediterranean indicates the existence of geography-related sub-generic diversity in which the Nemesia fauna of the eastern Mediterranean differs markedly from that of the western Mediterranean. While the eastern Mediterranean Nemesia fauna is highly homogeneous, the fauna of the western Mediterranean is very diverse. The eastern and western Nemesia faunae appear to overlap in the central Mediterranean. Efforts to relate the specific bulb types to the particular types of spermathecae described here were only partly successful.