590 Tiere (Zoologie)
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Twelve species of Platypalpus Macquart are described as new to science from different regions in Morocco: P. atlasensis sp. nov., P. brevicornoides sp. nov., P. ebejeri sp. nov., P. fatnae sp. nov., P. pauli sp. nov., P. imlilensis sp. nov., P. miroslavi sp. nov., P. moroccensis sp. nov., P. nigritellus sp. nov., P. rifensis sp. nov., P. shamshevi sp. nov. and P. taninensis sp. nov. Platypalpus albocapillatus Fallén, 1815 and P. boreoalpinus Frey, 1943 are recorded here for the first time from the whole of North Africa, with the first report of P. verbekei Grootaert & Chvála, 1992 from Morocco. Some species newly recorded from new biogeographical areas within the country are also reported here. Descriptions and illustrations of new species are provided, as well as distributions of all species recorded from Morocco.
Species of the cleptoparasitic bee genus Triepeolus Robertson, 1901 (Hymenoptera: Apidae: Nomadinae) of which the female has a trapezoidal or triangular pseudopygidial area with bright, reflective setae and a concave apical margin are revised. This entirely New World group includes the widely known species T. simplex Robertson, 1903 and is thus termed the simplex species group. A total of 18 species in the T. simplex group are recognized as valid, of which seven are newly named and described—T. apache sp. nov., T. eumeniformis sp. nov., T. hirsutus sp. nov., T. oblongimacula sp. nov., T. parahirsutus sp. nov., T. paucipunctatus sp. nov., and T. shoshone sp. nov., all from North America. Eleven redundant names are newly synonymized under three valid ones as follows: Epeolus rugulosus Cockerell, 1917 syn. nov., E. metatarsalis Friese, 1921 syn. nov., and T. bilunatus Cockerell, 1949 syn. nov. under Triepeolus mexicanus (Cresson, 1878); E. lectiformis Cockerell, 1925 syn. nov., T. lusor Cockerell, 1925 syn. nov., and T. junctus Mitchell, 1962 syn. nov. under T. rhododontus Cockerell, 1921; and E. permixtus Cockerell, 1923 syn. nov., T. brunnescens Cockerell & Sandhouse, 1924 syn. nov., T. pacis Cockerell, 1925 syn. nov., E. sarothrinus Cockerell, 1929 syn. nov., and E. sarothrinus var. confluens Cockerell, 1929 syn. nov. under T. segregatus (Cockerell, 1900). Species limits were established using an integrative systematics approach, namely considering morphological and biogeographic evidence as well as DNA barcode data. Taxon concepts are revised for all species in the T. simplex group, with morphological diagnoses and keys presented to enable their identification. Known information on the ranges and ecology of the treated species is summarized.
Isostichopus badionotus (Selenka, 1867) is distributed in the Atlantic Ocean. It has been recognized as a species with highly variable intraspecific coloration. To clarify taxonomic confusion and show the characters for correct identification of this valuable species, mitochondrial DNA (16S and COI), color patterns, external and internal morphology, ossicles, and habitat were examined in specimens from museum collections and from original sampling. As part of the revision, I. fuscus (Ludwig, 1875) from the Eastern Pacific Ocean and I. macroparentheses (Clark, 1922) from the Caribbean Sea, the only other two species currently recognized in the genus Isostichopus, were included. It was concluded that I. fuscus and I. macroparentheses are distinct and valid species, and that I. badionotus consists of two species: I. badionotus and I. maculatus (Greeff, 1882), previously synonymized as I. baqdionotus by Clark (1922). Isostichopus maculatus includes two subspecies, the nominal I. maculatus maculatus (Greeff, 1882) and I. maculatus phoenius (Clark, 1922), described as Stichopus badionotus var. phoenius Clark, 1922. Isostichopus maculatus maculatus, distributed in the East Atlantic, is very similar to I. maculatus phoenius, but differs in DNA characters, color pattern, and the size and shape of the tables in the dorsal papillae. Isostichopus maculatus phoenius, widely distributed in the Caribbean Sea and the Gulf of Mexico, is sympatric with I. badionotus, has similar ossicles but is clearly distinguished by its DNA sequences, color patterns, and habitat preferences. For the first time, ossicles from internal organs are described for Isostichopus, enhancing original species descriptions. Distribution maps, habitat, biology, conservation status, and a taxonomic key for distinguishing these species to aid their fishery management and aquaculture are presented.
India is a large country in Asia, and covers the transition zone between the Palaearctic and Indomalayan biogeographic realms, with influences from both. Present in India are members of the genus Andrena, an enormous bee genus distributed predominantly throughout the Holarctic, with the greatest Indian diversity in the Himalayan region due to its Palaearctic influences. Despite early studies in the late 19th and early 20th centuries, there has been almost no work on this group in India during the past century. A revision of type and non-type museum material combined with new collections has produced a revised total of 36 species of Andrena for India, including 11 species reported for the first time as well as the newly described Andrena (Melandrena) kedarnatha Wood & Gautam sp. nov. (northern India and Nepal) and Andrena (Simandrena) tungnatha Wood & Gautam sp. nov. (northern India). The true holotype of A. (Euandrena) communis Smith, 1879 is definitively located. Andrena burkelii Bingham, 1908 is synonymised with A. (Pallandrena) morosa Cameron, 1897. Lectotypes are designated for A. (Euandrena) murreensis Cockerell, 1923 and A. (incertae sedis) comberima beharica Cockerell, 1920. Further comments are made on the status of Andrena taxa described from India for which type material is and is not currently available. Thirty additional Andrena taxa suggested as present in the Indian fauna are excluded as either erroneous or lacking supporting data. These results illustrate the extent to which study of the Indian Andrena fauna has been confused, and provide a more stable taxonomic base for future studies in this country.
Two previously unrecognized species attributable to the genus Kontrimavichusia Makarikov & Binkienė, 2022 in arvicoline rodents from the North Caucasus are described. Kontrimavichusia testiculata sp. nov. is described from Microtus majori (Thomas, 1906) from the northwestern Caucasus (Republic of Adygeya and Karachay-Cherkess Republic, Russia) and Kontrimavichusia hobergi sp. nov. is described from Microtus daghestanicus (Shidlovsky, 1919) from the central Caucasus (Republic of North Ossetia, Russia). Kontrimavichusia testiculata is readily distinguishable from K. asymmetrica (Janicki, 1904) and K. hobergi in having a larger number of testes (4–6 per proglottis), larger suckers and a longer cirrus and cirrus-sac. In addition, the new species differs from its congeners by the position of the cirrus-sac with regard to the poral osmoregulatory canals and position of distal end of the rostellar pouch relative to the posterior margins of the suckers. Kontrimavichusia hobergi can be readily distinguished from its congeners by the arrangement of the testes in a triangle and the position of the cirrus-sac with regard to the poral osmoregulatory canals. In addition, this previously unrecognized species differs from K. asymmetrica and K. testiculata by the smaller dimensions of the fully developed strobila and a narrower ovary. The cirrus-sac of K. hobergi is larger than that in K. asymmetrica but smaller than that in K. testiculata. We also used partial sequences of the nuclear ribosomal 28S rRNA gene and mitochondrial nad1 gen to justify the generic arrangement and independent status of these two new species which are characterized in the current manuscript.
The genus Lissocnemis Kohl, 1907 of the subfamily Ctenocerinae is recorded from Korea for the first time. The diagnosis and characteristics of the genus, description of a new species, L. koreana Kim & Shimizu sp. nov. and redescription of another species, L. brevipennis hitherto known from Southeast Asia and Japan, are presented. The biogeographical distribution of the genus is discussed. Cryptosalius Turner, 1917 (type species: Pseudagenia rava Bingham, 1896; in part) and Dinagenia Banks, 1934 (type species: D. apollo Banks, 1934) are synonymized with Lissocnemis and the following new combinations are made: Lissocnemis tonkinensis (Turner, 1920) comb. nov. (= Cryptosalius tonkinensis Turner, 1920); Lissocnemis apollo (Banks, 1934) comb. nov. (= Dinagenia apollo Banks, 1934); and Lissocnemis satyrus (Banks, 1938) comb. nov. (= Dinagenia satyrus Banks, 1938). Lastly, L. satyrus (Banks, 1938) and L. nigricoxis Haupt, 1941 are rendered to be junior synonyms of L. apollo (Banks, 1934) comb. nov.
Due to the fragility of the ophiuroid (brittle star) skeleton, the bulk of the group’s fossil record consists of dissociated ossicles preserved as microfossils. In spite of their great potential as basis for taxonomic and phylogenetic studies, however, ophiuroid ossicles from the Paleozoic have received very little attention so far. Here, we provide an exhaustive taxonomic assessment of such fossils retrieved from sieving residues from the Silurian of Gotland, Sweden. This material was used in a previous study to describe two key taxa that allowed constraining the origin of the extant ophiuroid clade. The remaining taxa belonging to that same lineage are described in the present paper. The evidence at hand suggests that the stem of the extant ophiuroid clade was formed by two genera, Ophiopetagno and Ophiolofsson gen. nov., including six and five species, respectively, and spanning at least the upper Llandovery through upper Ludlow. We conclude that Ophiopetagno and Ophiolofsson represent sister genera that coexisted through most of the Silurian in the shallow tropical seas of Gotland. They underwent repeated body size reductions in correlation with environmental perturbations, with Ophiopetagno paicei eventually giving rise to Muldaster haakei; the first member of the living Ophiuroidea. Herein, we also introduce two new clades, Ankhurida clade nov. and Ophiovalida clade nov., and the following eight new species: Ophiolofsson joelmciveri gen. et sp. nov., O. obituary gen. et sp. nov., O. immolation gen. et sp. nov., O. archspire gen. et sp. nov., O. hendersonorum gen. et sp. nov., Ophiopetagno bonzo sp. nov., O. kansas sp. nov., O. doro sp. nov.; and two probably new species in open nomenclature: Ophiopetagno sp. 1, and Ophiopetagno sp. 2.
Highlights
• A proteomic analysis of the mandibular glands of Shinisaurius crocodilurus and Corucia zebrata, was performed.
• Scanning electron microscopy of S. crocodilurus' teeth revealed a sharp ridge on the anterior surface, but no grooves.
• Scanning electron microscopy of C. zebrata teeth showed a flattened crown with a pointed cusp.
• Proteomic analysis of gland extracts of S. crocodilurus and C. zebrata showed absence of venom-derived peptides or proteins.
• Our results strongly support the non-venomous character of both S. crocodilurus and C. zebrata.
Abstract
Based on its phylogenetic relationship to monitor lizards (Varanidae), Gila monsters (Heloderma spp.), and the earless monitor Lanthanotus borneesis, the Chinese crocodile lizard, Shinisaurus crocodilurus, has been assigned to the Toxicofera clade, which comprises venomous reptiles. However, no data about composition and biological activities of its oral secretion have been reported. In the present study, a proteomic analysis of the mandibular gland of S. crocodilurus and, for comparison, of the herbivorous Solomon Island skink Corucia zebrata, was performed. Scanning electron microscopy (SEM) of the teeth from S. crocodilurus revealed a sharp ridge on the anterior surface, but no grooves, whereas those of C. zebrata possess a flattened crown with a pointed cusp. Proteomic analysis of their gland extracts provided no evidence of venom-derived peptides or proteins, strongly supporting the non-venomous character of these lizards. Data are available via ProteomeXchange with identifier PXD039424.
Highlights
• Proteomic analyses of submandibular gland extracts of two alligator lizards of the Anguidae family are reported.
• A conserved set of putative toxins was found in the submandibular gland extracts of Abronia lythrochila and A. graminea.
• Toxins evolved in oral secretions of paleo- and neoanguimorpha over more than 100 million years of Anguimorpha cladogenesis.
• Electron microscopy of pleurodont teeth of A. lythrochila showed no sign of groove, external opening or striations.
• Assessing the role toxins play in the ecology of extant anguimorph lizards deserves functional studies in natural prey.
Abstract
A useful approach to deepen our knowledge about the origin and evolution of venom systems in Reptilia has been exploring the vast biodiversity of this clade of vertebrates in search of orally produced proteins with toxic actions, as well as their corresponding delivery systems. The occurrence of toxins in anguimorph lizards has been demonstrated experimentally or inferred from reports of the toxic effects of the oral secretions of taxa within the Varanidae and Helodermatidae families. In the present study, we have focused on two alligator lizards of the Anguidae family, the Mexican alligator lizard, Abronia graminea, and the red-lipped arboreal alligator lizard, A. lythrochila. In addition, the fine morphology of teeth of the latter species is described. The presence of a conserved set of proteins, including B-type natriuretic peptides, cysteine-rich secretory proteins, group III phospholipase A2, and kallikrein, in submandibular gland extracts was demonstrated for both Abronia species. These proteins belong to toxin families found in oral gland secretions of venomous reptile species. This finding, along with previous demonstration of toxin-producing taxa in both paleo- and neoanguimorpha clades, provides further support for the existence of a handful of conserved toxin families in oral secretions across the 100+ million years of Anguimorpha cladogenesis.
Among the 44 genera of predatory stink bugs (Asopinae) described for the Old World, there is a notable lack of recent studies. In this research, we aim to fill this gap by investigating the taxonomic history and morphology of species of Cantheconidea. As results, we present the redescription of the genus and validate three species: C. humeralis, C. javana and C. mitis comb. nov. A lectotype for C. mitis is designated and comments on the type material are given. Additionally, we transfer four species from Cantheconidea to the genus Eocanthecona: E. acuta comb. nov., E. variabilis comb. nov., E. gaugleri comb. nov. and E. insularis comb. nov. To accommodate the unique characteristics of Cantheconidea cyanacantha, we describe a new genus, Cantheconesia Brugnera & Roca-Cusachs gen. nov., and transfer the species, resulting in Cantheconesia cyanacantha gen. et comb. nov. Our study provides detailed redescriptions of species and accompanying images to support taxonomic decisions and presents new distribution records.