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The adult stage of Helioandesia tarregai gen. et sp. nov. (Lepidoptera: Yponomeutoidea: Heliodinidae) is described and illustrated from the arid western slopes of the Andes of northern Chile. The larvae of H. tarregai gen. et sp. nov. feed as leaf skeletonizers on Mirabilis acuta (Reiche) Heimerl (Nyctaginaceae). The mostly gray forewing of H. tarregai gen. et sp. nov., ornamented with strongly bulging metallic spots, resembles that of the representatives of the mainly Nearctic Lithariapteryx Chambers, 1876. However, the latter lacks CuP in the forewing, has a single bristle in the female frenulum, and lacks a well-developed cornutus. Helioandesia gen. nov. clustered as sister to Neoheliodines Hsu, 2004 in a cladistic analysis, although no synapomorphies were found for this cluster, while Lithariapteryx was sister to Helioandesia gen. nov. + Neoheliodines based on two synapomorphies. The genetic distance between a DNA barcode sequence of H. tarregai gen. et sp. nov. and representatives of other genera of Heliodinidae Heinemann, 1877 was 9.0–12.5% (K2P), and a maximum likelihood analysis based on this molecular marker confirmed the placement of H. tarregai gen. et sp. nov. as a member of this micromoth family. This contribution represents the first confirmed record of Heliodinidae for Chile.
A new spider genus (Araneae: Linyphiidae: Erigoninae) from a tropical montane cloud forest of Mexico
(2021)
A new genus and species of spider (Araneae, Linyphiidae, Erigoninae) from a tropical montane cloud forest of Mexico is described from both male and female specimens, Xim trenzado gen. et sp. nov. A phylogenetic parsimony analysis situates Xim gen. nov. as a distinct genus among the distal Erigoninae. Xim gen. nov. is sister to a clade including Ceratinopsis, Tutaibo and Sphecozone, but differs from those genera by having a high cymbium, large paracymbium, short straight embolus, male cheliceral stridulatory striae widely and evenly spaced, both sexes with a post-ocular lobe, male with two series of prolateral macrosetae on femur I, and the female by having strongly oblong, u-shaped spermathecae.
We describe a new species of Cyrtodactylus on the basis of two specimens collected from Ta Kou Nature Reserve, Binh Thuan Province, southern Vietnam. Cyrtodactylus chungi sp. nov. is distinguished from the remaining Indochinese bent-toed geckos by a combination of the following characters: relatively small body size (SVL up to 68.5 mm); a continuous neckband; 5 or 6 irregular transverse dorsal bands; 11 or 12 bands on original tail; keeled tubercles present on dorsum, posterior limbs and tail; 17 or 18 irregular dorsal tubercle rows; 30 or 31 ventral scale rows; ventrolateral skin folds indistinct; an angular series of seven precloacal pores in male and six pitted, enlarged precloacal scales in female, each series separated by a diastema of undifferentiated scales from 4–6 enlarged, poreless femoral scales; median subcaudals slightly enlarged; 17–20 subdigital lamellae under the fourth toe. Based on molecular analyses of the fragment of mitochondrial gene cytochrome c oxidase subunit I (COI), the new species is recovered as the sister taxon to Cyrtodactylus cattienensis s. str. with a genetic divergence of more than 9%. In phylogenetic analyses, the new species is recovered as a member of the Cyrtodactylus irregularis species group.
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.
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).
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.
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.
Hemipogon s. str. (Apocynaceae: Asclepiadoideae) currently consists of three species sharing an erect herbaceous habit, narrow leaves and corona-less flowers with urceolate, internally bearded corolla, that are mainly distributed in savannahs of the Cerrado biodiversity hotspot, South America. Here, we describe and illustrate a new species of Hemipogon, H. trilobatus Bitencourt & Rapini sp. nov., from an open savannah in Chapada dos Veadeiros, Central Brazil. Hemipogon trilobatus sp. nov. differs from the other species of the genus mainly by the presence of a reduced staminal corona with 3-lobed lobes, but also by opposite leaves and triangular anthers. Distribution and habitat data, as well as a key and a comparative table to distinguish the four species currently accepted in Hemipogon s. str., are provided. Based on criteria B2ab(i,ii,iii,iv) of the International Union for Conservation of Nature (IUCN), the species is provisionally assessed as Critically Endangered.
Sweat bees in the subgenus Lasioglossum (Dialictus) are one of the most diverse and abundant bee taxa, and a critically important component of bee biodiversity. Yet, the most basic taxonomic knowledge of these bees is lacking in many regions. As a step towards a better understanding of the L. (Dialictus) of the western Nearctic region, a revision of the ‘red-tailed’ L. (Dialictus) species was completed. Thirty-six species were revised, 20 of which are described as new, and two names are treated as junior subjective synonyms. Descriptions, figures, distribution maps, floral hosts, and keys to species for females and males are provided. The following 20 species are described as new: Lasioglossum (Dialictus) arenisaltans sp. nov., L. (D.) argammon sp. nov., L. (D.) austerum sp. nov., L. (D.) cactorum sp. nov., L. (D.) cembrilacus sp. nov., L. (D.) clastipedion sp. nov., L. (D.) clavicorne sp. nov., L. (D.) decorum sp. nov., L. (D.) festinum sp. nov., L. (D.) imbriumbrae sp. nov., L. (D.) julipile sp. nov., L. (D.) lilianae sp. nov., L. (D.) meteorum sp. nov., L. (D.) miltolepoides sp. nov., L. (D.) minckleyi sp. nov., L. (D.) perditum sp. nov., L. (D.) rufornatum sp. nov., L. (D. ) spivakae sp. nov., L. (D.) tessellatosum sp. nov., and L. (D.) torrens sp. nov. Previously unknown males of L. (D.) clematisellum (Cockerell, 1904), L. (D.) droegei Gibbs, 2009, L. (D.) kunzei (Cockerell, 1898), and L. (D.) pallidellum (Ellis, 1914) are described and figured for the first time. Lasioglossum (Dialictus) clarissimum (Ellis, 1914) (= Halictus clarissimus Ellis, 1914) and L. (D.) perexiguum (Sandhouse, 1924) (= Halictus (Chloralictus) perexiguus Sandhouse, 1924) are new subjective junior synonyms of L. mesillense (Cockerell, 1898) (= Halictus nymphalis var. mesillensis Cockerell, 1898). A lectotype specimen is newly designated for L. mesillense, for which the location of the type material has not previously been known. The following five new records for Mexico are reported: L. clematisellum, L. droegei, L. eophilus (Ellis, 1914), L. kunzei, and L. pallidellum.
The genus Parasogata Zhou, Yang & Chen, 2018 is here reported from India represented by the new species Parasogata sexpartita sp. nov. collected in a recent exploration and survey of delphacids from Nagaland in northeastern India. A second species of Eoeurysa Muir, 1913 from India, the new species Eoeurysa sagittaria sp. nov., was found in Rampur, Una, Himachal Pradesh. Both new species are described with illustrations, and a molecular identification is given with the mtCOI gene sequence. A modified key to species of the genera is also provided.