Refine
Year of publication
- 2020 (35) (remove)
Document Type
- Article (35) (remove)
Has Fulltext
- yes (35)
Is part of the Bibliography
- no (35) (remove)
Keywords
- taxonomy (35) (remove)
Institute
Two new species of Psammoecus Latreille, 1829 from Australia are described: Psammoecus australis sp. nov. and P. venustus sp. nov. A taxonomic revision and diagnoses for other Australian species are provided. Psammoecus obesus Grouvelle, 1919 is recorded from Australia for the first time. Two new synonyms are discovered: Psammoecus t-notatus Blackburn, 1908 = P. amoenus Grouvelle, 1912 syn. nov.; Psammoecus vittifer Blackburn, 1903 = P. concolor Grouvelle, 1919 syn. nov. A lectotype is designated for Psammoecus concolor Grouvelle, 1919.
An annotated list of twenty species of rarely collected and little known bees of the genus Sphecodes Latreille, 1804 (Hymenoptera: Apoidea: Halictidae) from the Himalayas is given. Sphecodes bluethgeni sp. nov. is described from Bhutan. Three species are newly recorded from the Himalayas: S. binghami Blüthgen, 1924, S. kershawi Perkins, 1921 and S. laticeps Meyer, 1920. Based on type specimens, new synonymies have been proposed for Sphecodes cameronii (Bingham, 1897) = S. armeniacus Warncke, 1992 syn. nov.; S. gibbus (Linnaeus, 1758) = S. indicus Bingham, 1898 syn. nov.; and S. invidus (Cameron, 1897) = S. nigrobasalis Meyer, 1922 syn. nov. A lectotype is designated for Sphecodes sikkimensis Blüthgen, 1927. Illustrated keys to males and females of all species known from the Himalayas and an updated checklist of the 26 Himalayan species of Sphecodes are provided. Additionally, one new species from neighboring Uttar Pradesh (India), Sphecodes uttaricus sp. nov., is here described as new and included due to its close relationship to the Himalayan S. sikkimensis Blüthgen, 1927.
A new species of snail-eating snakes of the genus Pareas Wagler, 1830 is described from the eastern Himalayas. The species Pareas kaduri sp. nov. differs from all known species of the genus in bearing the following suite of characters: SVL 455–550 mm, TaL/TL 0.184–0.207, brown dorsum with black transverse bands throughout the body, 15 dorsal scale rows throughout the body and mid-dorsal vertebral scale rows enlarged, 8 rows keeled in males, loreal not touching orbit, ventrals 160–183, subcaudals 65–70 in males, 52 in one female specimen, hemipenis short, unilobed and 6–7 maxillary teeth. Molecular data for mitochondrial 16S rRNA and cytochrome b genes further attest the distinctness of the new species, which was recovered as a member of the Pareas hamptoni clade. Our work brings the total number of species recognized within the genus Pareas to 20.
Thirteen species of Echinoderes with nearly identical spine/tube patterns, and apparently similar tergal extensions were re-examined and compared. Based on this, redescriptions and/or emended species diagnoses are provided for Echinoderes aureus, E. dujardinii, E. gerardi, E. imperforatus, E. pacificus, E. pilosus, E. sensibilis, E. sublicarum and E. worthingi, and new details about cuticular structures are added for E. kozloffi and E. gizoensis. The new information derived from the redescriptions, and the subsequent comparative studies revealed that: 1) the holotype of Echinoderes lanceolatus is identical with the types of Echinoderes aureus, and E. lanceolatus is thus a junior synonym of E. aureus; other potentially synonymous species that should be addressed further in the future include: E. dujardinii + E. gerardi; E. imperforatus + E. sensibilis, and E. pacificus + E. sublicarum; 2) the paratypes of E. lanceolatus represented a different yet undescribed species, here described as E. songae Sørensen & Chang sp. nov.; 3) a comparison with literature information about E. ehlersi showed that the species is so insufficiently described that a redescription of topotype material is required before the species should be considered for taxonomic comparison; 4) specimens from the Andaman Islands, India, that previously have been reported as Echinoderes cf. ehlersi represent two different undescribed species, of which one is described as E. chandrasekharai Sørensen & Chatterjee sp. nov. and the other is left undescribed due to the limited material available; 5) out of a total of fifteen addressed species, it is proposed that eleven represent a putatively monophyletic group that is named the Echinoderes dujardinii group. The group includes following species: E. dujardinii, E. ehlersi, E. gerardi, E. imperforatus, E. kozloffi, E. sensibilis, E. pacificus, E. sublicarum, E. songae Sørensen & Chang sp. nov., E. chandrasekharai Sørensen & Chatterjee sp. nov., and Echinoderes sp. from the Andaman Islands, and is supported by a similar spine/tube pattern (except for variation regarding the presence of lateral accessory tubes on segment 8); generally short middorsal spines, especially on segments 4 to 6; glandular cell outlets type 1 always present in middorsal positions on segments 1 to 3, and in subdorsal positions on segments 4 to 9; glandular cell outlets type 2 always present in laterodorsal or midlateral positions on segment 8, and sometimes in same positions on segment 9 but never at any other segments or positions; female papillae always present on sternal plates of segments 7 and 8, and occasionally also on segment 6; tergal extensions well-spaced, triangular, gradually tapered cones, and pectinate fringes of sternal extensions are differentiated into seta-like tufts. The comparisons furthermore showed potential taxonomic significance of two echinoderid character traits that previously have been slightly neglected as diagnostic traits, namely the presence and appearance of female papillae, and the dorsal pattern of glandular cell outlets type 1. Female papillae may occur on the sternal plates of segments 6 to 8, but the positions may differ from ventrolateral to ventromedial, and the morphology of the intracuticular substructure also differ at species level. Information about position and morphology of female papillae proved helpful for species recognition, but it might also provide information of phylogenetic importance. Analyses of glandular cell outlet type 1 patterns on the dorsal sides of segments 1 to 9 in species of Echinoderidae, revealed several apparently unique or rare patterns, but also three distinct patterns that applied to larger groups of species. One pattern is the one present in all species of the E. dujardinii group, whereas the other two common patterns included 1) middorsal outlets on segments 1 to 3, and paradorsal outlets on segments 4 to 9 (found in 27 species), and 2) middorsal outlets on segments 1 to 3, 5 and 7, and paradorsal outlets on segments 4, 6 and 8 to 9 (found in 27 species).
The species of the Eumerus tricolor species group in Iran are reviewed. Six species new to science are described from Iran, i.e., Eumerus atricolorus Gilasian & van Steenis sp. nov., E. brevipilosus Gilasian & van Steenis sp. nov., E. chekabicus Gilasian & van Steenis sp. nov., E. ovoformus Gilasian & van Steenis sp. nov., E. pilosipedes Gilasian & van Steenis sp. nov. and E. vallicolus Gilasian & van Steenis sp. nov. Three species, E. hissaricus Stackelberg, 1949, E. longitarsis Peck, 1979 and E. richteri Stackelberg, 1960, are newly recorded from Iran. Photographs of the species as well as illustrations of the male genitalia of the new species and closely related species are provided. An identification key to the males of the Iranian Eumerus tricolor species group is presented. A row of long posterodorsal setae on the wing vein costa basally is presented and argued as a new diagnostic morphological character for the entire Eumerus tricolor species group.
A new millipede species of the genus Sechelleptus Mauriès, 1980 is described and illustrated from Mayotte Island, Indian Ocean. This new species, S. arborivagus sp. nov., found on trees, looks particularly similar to the sympatric S. variabilis VandenSpiegel & Golovatch, 2007, but is much larger and has a very different ecological behavior. Phylogenetic analyses based on a concatenated dataset of the COI and 16S rRNA genes and including nine species of Spirostreptidae (including Sechelleptus, Doratogonus Attems, 1914, Bicoxidens Attems, 1928 and Spirostreptus Brandt, 1833), strongly support the monophyly of Sechelleptus. Despite the similarity of their genitalia, the molecular analyses also reveal a clear-cut genetic divergence between S. arborivagus sp. nov. and S. variabilis (22.55% for COI and 6.63% for 16SrRNA) and further suggest the presence of a higher diversity within the genus Sechelleptus on Mayotte.
The Chinese fauna of the pselaphine genus Sathytes Westwood (Batrisitae: Batrisini) currently includes 20 species. In this paper, 15 new species from various provinces of the country are described: S. alpicola sp. nov. (Xizang), S. australis sp. nov. (Guangdong, Guangxi), S. chayuensis sp. nov. (Xizang), S. chengzhifeii sp. nov. (Yunnan), S. huapingensis sp. nov. (Guangxi), S. linzhiensis sp. nov. (Xizang), S. maoershanus sp. nov. (Guangxi), S. nujiangensis sp. nov. (Yunnan), S. panzhaohuii sp. nov. (Xizang), S. shennong sp. nov. (Hubei), S. tianquanus sp. nov. (Sichuan), S. transversus sp. nov. (Xizang), S. valentulus sp. nov. (Guangxi), S. xingdoumontis sp. nov. (Hubei) and S. xizangensis sp. nov. (Xizang). New collection records are provided for S. longitrabis Yin & Li, 2012, S. tangliangi Yin & Li, 2012 and S. yunnanicus Yin & Li, 2012. Maps showing the distribution of the genus in China, and an updated checklist of the world species are provided.
The Isla Sala y Gómez or Motu Motiro Hiva is located 415 km northeast of Rapa Nui (Easter Island) and 3420 km from the coast of northern Chile. It is a small oceanic island (2.5 km2) dominated by volcanic rock with very little vegetal cover. Here, we describe the first endemic arachnid for the island, Ariadna motumotirohiva sp. nov. Females are similar to those of Ariadna perkinsi Simon, 1900 from Hawaiʻi and Ariadna lebronneci Berland, 1933 from the Marquesas in the dorsal dark abdominal pattern, but they differentiate from the latter in the anterior receptaculum, promarginal cheliceral teeth and leg IV macrosetae. A recent survey of the arachnid fauna of Rapa Nui, which included Motu Nui and the rocky shores, did not record the presence of the family Segestriidae, neither has it been found during previous surveys. However, it is not possible to discard the possibility of a local extinction on Rapa Nui and survival on Sala y Gómez. This study suggests other endemic terrestrial arthropods could be present on this very small and remote island.
This paper describes and illustrates two new nematode species of the genus Paratrilobus Micoletzky, 1922. The species Paratrilobus tankhoyensis sp. nov. was found at the estuary of the Pereyomnaya River (water area of Lake Baikal, near the Tankhoy railway station). Paratrilobus tankhoyensis sp. nov. is most similar to P. expugnator (Tsalolichin, 1976) in the body size, but differs in the comparatively thin body, shorter and thicker tail, shorter stoma and spicules. Another new species, Paratrilobus aquaticus sp. nov., was found in Posolsk Bank (natural underwater elevation of the bottom between the southern and central basins of Lake Baikal). The species is similar to P. granulosus Gagarin & Naumova, 2011 and P. ultimus (Tsalolichin, 1977) in the structure of the precloacal supplements. It differs from the former in the absence of crystalloids, a comparatively longer pharynx, longer stoma and outer labial setae as well as the absence of subterminal seta. It differs from the latter in a longer pharynx, stoma and longer outer labial setae as well as a longer and more slender tail. We also discuss diagnostic features of the males of the genus Paratrilobus.
The widespread Ophioderma hendleri sp. nov., from the Eastern Tropical Pacific (Mexico to Colombia) is distinguished from its congeners by having radial shields covered by granules, naked adoral shields, up to 11 arm spines, and by its brown and beige coloration. Ophioderma hendleri sp. nov. belongs to the group of species with naked adoral shields (i.e., O. pentacanthum H.L. Clark, 1917, O. variegatum Lütken, 1856), and it has frequently been misidentified as O. panamense Lütken, 1859 or O. variegatum. Therefore, the main aim of the present work was to describe Ophioderma hendleri sp. nov. and differentiate it from its congeners. The original description of O. panamense was incomplete; thus, we provide a redescription. Due to the confusion in previous designations of its type material, we designate a lectotype and paralectotype of O. variegatum. Finally, we expand the distribution range of O. pentacanthum to Cocos Island, Costa Rica. With this work, the total number of valid species of Ophioderma Müller & Troschel, 1840 in the world increases to 33 and in the Eastern Pacific to nine species.