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Improving nomenclatural consistency: a decade of experience in the World Register of Marine Species
(2017)
The World Register of Marine species (WoRMS) has been established for a decade. The early history of the database involved compilation of existing global and regional species registers. This aggregation, combined with changes to data types and the changing needs of WoRMS users, has resulted in an evolution of data-entry consistency over time. With the task of aggregating the accepted species names for all marine species approaching completion, our focus has shifted to improving the consistency and quality of data held while keeping pace with the addition of > 2000 new marine species described annually. This paper defines priorities and longer-term aims that promote standardisation within and interoperability among biodiversity databases, provides editors with further information on how to input nomenclatural data in a standardised way and clarifies for users of WoRMS how and why names are represented as they are. We 1) explain the categories of names included; 2) list standard reasons used to explain why a name is considered ‘unaccepted’ or ‘uncertain’; 3) present and explain the more difficult situations encountered; 4) describe categories of sources and notes linked to a taxon; and 5) recommend how type material, type locality and environmental information should be entered.
Siamopsis gen. nov., described here, belongs to a group of genera with the right valve overlapping the left valve in the subfamily Cypridopsinae Kaufmann, 1900 of the family Cyprididae Baird, 1845. The distinguishing characters of the new genus are in the morphology of its valves and soft parts. The postero-dorsal margin of the internal left valve is plate-like protruded. The morphology of this plate varies in different species, e.g., some species bear a tooth-like tubercle on the plate. The posterior margin of the right valve is recurved inwardly at ca mid-height, resulting in the occurrence of a lobe-like expansion that can clearly be seen in the dorsal and caudal views of the carapace. In addition, the other diagnostic soft part features of the new genus are the cylindrical caudal ramus, the presence of two t-setae on the female A2 penultimate segment, the very elongated terminal segment of the Mx1 palp, the morphology of the two large bristles (tooth bristles) of the Mx1 third endite (one smooth, one serrated) and the absence of d-seta on T1. In the present paper, five new species are described under this new genus: Siamopsis renateae gen. et sp. nov., S. suttajiti gen. et sp. nov., S. conspecta gen. et sp. nov., S. khoratensis gen. et sp. nov. and Siamopsis planitia gen. et sp. nov. A key to the species of Siamopsis gen. nov. is also provided.
Two species of the nematode family Diplopeltidae are described from Skagerrak. The new genus Belgopeltula gen. nov. is proposed for Diplopeltula belgica Vincx & Gourbault, 1992 and is characterised by: amphidial fovea circular in female and double-loop-shaped in male; excretory pore located at the level of cephalic setae bases; oral opening on the dorsal side of the body; pharynx subdivided into strongly muscularised fusiform corpus and weakly muscularised narrow and long postcorpus; female didelphic with antidromously reflexed ovaries; supplements absent. Mudwigglus micramphidium sp. nov. is characterised by: a body of 0.6 mm long; cephalic sensilla 1.5 μm long; amphidial fovea loop-shaped, 8 μm long and 3.5 μm wide; gymnostom without cuticularised ring; tail elongate conoid, with subcylindrical distal part; terminal setae absent; spicules 15 μm long; gubernaculum present; two midventral precloacal setae. It is distinguished from M. macramphidium Leduc, 2013 in having shorter amphidial fovea, shorter spicules and presence of two precloacal setae. Redescription of Diplopeltis cylindricauda Allgén, 1932 is provided based on type material. Diplopeltula minuta Vitiello, 1972 is transferred to the genus Mudwigglus Leduc, 2013. Diplopeltis cylindricauda Allgén, 1932, Diplopeltula laminata Vitiello, 1972 and Diplopeltula cassidaignensis Vitiello, 1972 are transferred to the genus Pseudaraeolaimus Chitwood, 1951.
A new mesoserphid wasp from the Middle Jurassic of northeastern China (Hymenoptera, Proctotrupoidea)
(2017)
A new genus and species of Mesoserphidae (Hymenoptera), Juraserphus modicus gen. et sp. nov., is described based on a well-preserved fossil specimen from the Middle Jurassic Jiulongshan Formation of northeastern China. It is characterized by the following forewing features: the forking of Rs+M located approximately one-third of the distance between 1m-cu and 2r-rs, both 1cu-a and 2cu-a antefurcal; 1-M more than twice as long as 1m-cu and hind wing with cells r and rm closed. In addition, it has a short ovipositor, only extending slightly beyond the metasomal apex. Its new morphological characters broaden the diversity of Mesoserphidae in the Mesozoic and provide new insights into the evolution and relationships of Mesoserphidae.
Daddy-long-leg giants: revision of the spider genus Artema Walckenaer, 1837 (Araneae, Pholcidae)
(2017)
This is the first revision of Artema Walckenaer, 1837, a genus consisting of large and phylogenetically interesting species. Even though Artema is not species-rich (now eight nominal species), it has suffered from poor descriptions and synonymies. Our main goal was to gather all available material and to clarify species limits. Four species are easily distinguished from other congeners: Artema atlanta Walckenaer, 1837, the type species; A. kochi Kulczyński, 1901 (revalidated); A. bunkpurugu Huber & Kwapong, 2013; and A. nephilit sp. nov. All other species are problematic for varying reasons: species limits are unclear between A. doriae Thorell, 1881 and A. transcaspica Spassky, 1934; A. magna Roewer, 1960 and A. ziaretana (Roewer, 1960) are problematic because they are based on female and juvenile types respectively and little new material is available. The material available to us suggests the existence of a few further species; however, they are not formally described, either because of small sample sizes (Artema sp. a and A. sp. b are represented by only one specimen each) or because of unclear species limits (between Artema sp. c, A. transcaspica and A. doriae).This study is the first serious step towards understanding the genus. Intensive collecting effort is needed in order to fully clarify species limits.
Hornbeams (Carpinus) and hop-hornbeams (Ostrya) are trees or large shrubs from the northern hemisphere. Currently, 43 species of Carpinus (58 taxa including subdivisions) and 8 species of Ostrya (9 taxa including sudivisions) are recognized. These are based on 175 (plus 16 Latin basionyms of cultivars) and 21 legitimate basionyms, respectively. We present an updated checklist with publication details and type information for all accepted names and the vast majority of synonyms of Carpinus and Ostrya, including the designation of 54 lectotypes and two neotypes. Cultivars are listed if validly described under the rules of the ICN. Furthermore, we consider Carpinus hwai Hu & W.C.Cheng to be a synonym of Carpinus fargesiana var. ovalifolia (H.J.P.Winkl.) Holstein & Weigend comb. nov. During the course of our work, we found 30 legitimate basionyms of non-cultivars that have been consistently overlooked since their original descriptions, when compared with the latest checklists and floristic treatments. As regional floras are highly important for taxonomic practice, we investigated the number of overlooked names and found that 78 basionyms were omitted at least once in the eight regional treatments surveyed. More seriously, we found 4 basionyms of accepted species being overlooked in a major floristic treatment.
Ufocandona hannaleeae gen. et sp. nov. (Crustacea, Ostracoda) from an artesian well in Texas, USA
(2017)
We describe a new genus, Ufocandona gen. nov. with its type species Ufocandona hannaleeae gen. et sp. nov., from an artesian well in San Marcos, Texas, USA. The new genus has diagnostic characteristics that distinguish it from other genera in Candonidae, including the asymmetric shape of the valves, the smooth central area on the external surface of the valves, the hexagonal ornamentations around the marginal ends of the carapace, the dense spines on the marginal edges of the right valve and the dorsal prolongation and tubercles seen from inside the ventral edges of the left valve. Additional differences in the soft body parts of the male and female (e.g., claw-like uropod, shape of hemipenis, long Y aesthetascs, two short or reduced exopods on antenna, reduced numbers of setae and segments on other extremities) distinguish the new genus from others in the family. The discovery of this species from a deep artesian well contributes important information to our understanding of groundwater species diversity in a biologically diverse aquifer where the ostracod fauna has been unstudied.
Eight species of Diplopeltoides are described from the Swedish west coast. Diplopeltoides suecicus sp. nov. has the cuticle with longitudinal striation visible only under SEM; cuticular plate underlying the cephalic cuticle around the amphid present; cephalic sensilla 4–6 μm long; amphid an inverted U-shape; wide space between amphidial branches areolated; spicules 27–31 μm long; gubernaculum with caudal apophysis. Diplopeltoides longicaudatus sp. nov. is characterized by a cuticle without longitudinal striation; cuticular plate underlying cephalic cuticle around amphid present; cephalic sensilla 13 μm long; amphid an inverted U-shape; narrow space between amphidial branches not ornamented; spicules unequal in size, 27–31 μm long; gubernaculum absent; midventral precloacal cuticular ridge present. D. grandis sp. nov. is characterized by a cuticle with longitudinal striation; cuticular plate underlying cephalic cuticle around amphid present; cephalic sensilla 18.5 μm long; amphid an inverted U-shape; wide space between amphidial branches punctate. The following taxonomic changes are proposed: Diplopeltoides asetosus (Juario, 1974) comb. nov., Diplopeltoides botulus (Wieser, 1959) comb. nov., Diplopeltoides bulbosus (Vitiello, 1972) comb. nov., Diplopeltoides lucanicus (Boucher & Helléouët, 1977) comb. nov., Diplopeltoides pumilus (Vincx & Gourbault, 1992) comb. nov. and Diplopeltoides striatus (Gerlach, 1956) comb. nov. Diplopeltoides holovachovi Fadeeva & Mordukhovich, 2013 is synonymised with Diplopeltoides pumilus comb. nov. An updated key to the species of Diplopeltoides is provided.
A new species of the genus Spinaethorax Papáč & Palacios-Vargas, 2016, recently erected for two cave species in Mexico, is described from a Vietnamese cave. It differs from the Mexican species most noticeably by the dorsal chaetotaxy of the head (number and morphology of chaetae), the shape of S-chaetae on the third antennomere, the dorsal chaetotaxy of the abdomen and the chaetotaxy of the dens. The pattern of special τ-chaetae is described for the first time in the genus. The affinities between Spinaethorax and the other genera of Neelipleona are discussed. Spinaethorax is propably closely related to Neelus Folsom, 1896. A table of the differential characters is provided for the three known species of Spinaethorax. Spinaethorax appears to be restricted to caves, but its presence in Vietnam indicates that this genus has a much larger distribution than previously recognized.
The genus Dasydorylas Skevington, 2001 is recorded from two provinces in Iran (Sistan-o Baluchestan and Kermanshah Provinces). Dasydorylas derafshani sp. nov. and D. zardouei sp. nov. are characterized morphologically by DNA barcoding of the mitochondrial COI gene. Eudorylas antennalis Kapoor, Grewal & Sharma, 1987 is transferred to Dasydorlyas (comb. nov.). An existing identification key to the males of the western Palaearctic species of Dasydorylas is complemented to include the newly described species.