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The Afrotropical (including Malagasy Subregion) species of the genus Asobara Foerster, 1863, are revised. In addition to the redescribed 15 known species, 25 new species are described and illustrated, viz., Asobara abyssiniensis Peris-Felipo, sp. nov., A. caboverdensis van Achterberg, sp. nov., A. carinata Peris-Felipo, sp. nov., A. cracentis van Achterberg, sp. nov., A. elongitarsis van Achterberg, sp. nov., A. fletcheri Peris-Felipo, sp. nov., A. harrinsmithensis Peris-Felipo, sp. nov., A. kawandensis Peris-Felipo, sp. nov., A. kibalensis van Achterberg, sp. nov., A. laticlypeata van Achterberg, sp. nov., A. mediana van Achterberg, sp. nov., A. mellicephalata van Achterberg, sp. nov., A. natalensis Peris-Felipo, sp. nov., A. notleyi Peris-Felipo, sp. nov., A. robusta van Achterberg, sp. nov., A. sarae Peris-Felipo, sp. nov., A. somersetensis Peris-Felipo, sp. nov., A. stubbsi Peris-Felipo, sp. nov., A. taylori Peris-Felipo, sp. nov., A. vanalpheni van Achterberg, sp. nov., A. vanharteni van Achterberg, sp. nov., A. victoriana Peris-Felipo, sp. nov., A. zaprionae van Achterberg, sp. nov., A. zimbabwana Peris-Felipo, sp. nov., A. zululana Peris-Felipo, sp. nov. Moreover, the following new combination is suggested: Asobara pulchricornis (Szépligeti, 1911) comb. nov. A key to all Afrotropical (including Malagasy) species is provided for the first time.
Revised definitions are given for the genus Mysidium Dana, 1852, and its eight previously known species, based on material from Curaçao, Bonaire and SE-Brazil, along with the evaluation of published data. Type material of Diamysis columbiae Zimmer, 1915, M. cubanense Băcescu & Ortiz, 1984 and M. rubroculatum Băcescu & Ortiz, 1984 is examined. A lectotype is designated for D. columbiae Zimmer, 1915, a senior synonym of Mysidium columbiae (Zimmer, 1915). Two new species are described, M. triangulare Wittmann sp. nov. from Curaçao and M. antillarum Wittmann sp. nov. from Curaçao and Bonaire. Known ranges are extended by first records of M. cubanense from Curaçao and Bonaire and of M. integrum W.M. Tattersall, 1951 from SE Brazil. Three morphologically different groups are established at the subgeneric level: (1) the nominotypical subgenus Mysidium Dana, 1852 with M. gracile (Dana, 1852), M. integrum, M. cubanense, M. rubroculatum and M. triangulare sp. nov. from the West Atlantic plus M. rickettsi Harrison & Bowman, 1987 from the East Pacific; (2) Occimysidium Wittmann subgen. nov. represented only by M. pumae Ortiz, Hendrickx & Winfield, 2017 from the Pacific coast of Mexico; and finally (3) Orientomysidium Wittmann subgen. nov. comprising M. columbiae and M. antillarum sp. nov. from the West Atlantic. The poorly known M. iliffei Băcescu, 1991 is not assigned to any subgenus. A key to the resulting three subgenera and ten nominal species of the genus Mysidium is given.
We revise the genus Attemsostreptus Verhoeff, 1941 based on type material of the type species, A. costatus Verhoeff, 1941, synonymise A. orobius (Kraus 1958) with A. costatus and describe a second species of the genus, A. reflexus sp. nov., collected from Kimboza Forest Reserve in Tanzania, and discuss the dubious tribe Trachystreptini.
Revision of the genus Cerapanorpa (Mecoptera: Panorpidae) with descriptions of four new species
(2019)
The genus Cerapanorpa Gao, Ma & Hua, 2016 is taxonomically revised. Cerapanorpa is confirmed to be endemic to the mountain regions in central China. Nineteen species are recognized in the genus, including four new species: Cerapanorpa baimaensis sp. nov., Cerapanorpa xuebaodinga sp. nov., and Cerapanorpa yanggashana sp. nov. from the Minshan Mountains, and Cerapanorpa taizishana sp. nov. from the northeastern margin of the Qinghai-Tibetan Plateau. Six species are transferred from Cerapanorpa back to Panorpa Linnaeus, 1758. An updated key to species is presented.
We examined the type specimens and historical collections holding puzzling Atlantic and Mediterranean material belonging to the genus Schizoretepora Gregory, 1893. We performed a detailed study of the colonial characters and re-describe the resulting species and those that have rarely been found or have poor original descriptions. As a result of this revision, nine species are found in the northeast Atlantic and Mediterranean. Six of them are re-described and illustrated: S. aviculifera (Canu & Bassler, 1930), S. calveti d’Hondt, 1975, S. imperati (Busk, 1884), S. sp. nov.? (= S. imperati sensu O'Donoghue & de Watteville 1939) (in open nomenclature, specimen lacks ovicells), S. pungens (Canu & Bassler, 1928) and S. solanderia (Risso, 1826). For S. dentata (Calvet, 1931), no material remains; furthermore, S. hassi Harmelin, Bitar & Zibrowius, 2007 and S. serratimargo (Hincks, 1886) have recently been described and redescribed, respectively. This new arrangement attains a coherent geographical distribution: S. imperati seems restricted to the eastern Atlantic, S. dentata and S. calveti are deepwater species from Atlantic islands, S. pungens and S. aviculifera dwell on the African coasts of the Western Mediterranean, S. hassi and S. sp. nov.? (=S. imperati sensu O’Donogue & de Wateville 1939) are confined to the Eastern Mediterranean, and S. solanderia and S. serratimargo live on the European coasts of the Mediterranean.
Revision of the land snail genus Landouria Godwin-Austen, 1918
(Gastropoda, Camaenidae) from Java
(2019)
A revision of the land snail genus Landouria Godwin-Austin, 1918 (Camaenidae) from Java reveals that this group represents the most diverse land snail radiation on that island. Only six species of Landouria were recognized from Java in the last revision of the genus based on shell characters. Our investigation, which also considers the genitalia as well as DNA sequences, shows that the diversity in Java is much higher. Based on newly collected specimens as well as museum material, twenty-eight species of Landouria from Java are described and figured. To stabilize the nomenclature, neotypes are designated for L. winteriana (Pfeiffer, 1842) and L. rotatoria (Pfeiffer, 1842). Sixteen species are described as new to science, i.e., L. naggsi sp. nov., L. parahyangensis sp. nov., L. nusakambangensis sp. nov., L. petrukensis sp. nov., L. tholiformis sp. nov., L. madurensis sp. nov., L. abdidalem sp. nov., L. sewuensis sp. nov., L. tonywhitteni sp. nov., L. sukoliloensis sp. nov., L. nodifera sp. nov., L. pacitanensis sp. nov., L. zonifera sp. nov., L. pakidulan sp. nov., L. dharmai sp. nov. and L. menorehensis sp. nov. Landouria conoidea (Leschke, 1914) comb. nov., L. intumescens (Martens, 1867) comb. nov., L. moussoniana (Martens, 1867) comb. nov., L. schepmani (Möllendorff, 1897) comb. nov. and L. leucochila (Gude, 1905) comb. nov. are considered valid species of the genus Landouria for the first time. Plectotropis kraepelini Leschke, 1914 syn. nov. is considered a probable synonym of L. winteriana (Pfeiffer, 1842), P. trichotrochium Möllendorff, 1897 syn. nov. is a synonym of L. epiplatia (Möllendorff, 1897) and the preoccupied name Helix squamulosa Martens, 1867 syn. nov. is a synonym of L. madurensis sp. nov. We estimate that there are actually more than fifty species of Landouria in Java because many shell samples could not be classified and because no material is available from several regions of the island. A molecular phylogeny reveals that the species from Java do not form a monophyletic group, but that at least one species from Timor is nested within Javanese clades. This means that the Oriental Landouria crossed Wallace's line, the supposed border between the Oriental and Australo-Papuan regions, at least twice and supports the conclusion that Wallace's line does not represent a more severe barrier for terrestrial organisms than other straits through the archipelago. Within the Javanese clades, species from western and eastern Java are mixed, indicating frequent dispersals also within Java.
We provide the first comprehensive taxonomic revision of the poorly known South American butterfly genus Zischkaia Forster, 1964, hitherto regarded as including three described species. A phylogenetic analysis based on DNA sequence data shows that Zischkaia is monophyletic and consists of two morphologically diagnosable clades. Morphological characters and DNA 'barcodes' support the recognition of twelve species in the genus, a significant increase even for the relatively poorly studied subtribe Euptychiina. Consequently, nine new species are described and named herein, including Z. arctoa Nakahara, sp. nov., Z. chullachaki Nakahara & Zacca, sp. nov., Z. baku Zacca, Dolibaina & Dias, sp. nov., Z. arenisca Nakahara, Willmott & Hall, sp. nov., Z. argyrosflecha Nakahara, L. Miller & Huertas, sp. nov., Z. abanico Nakahara & Petit, sp. nov., Z. josti Nakahara & Kleckner, sp. nov., Z. mielkeorum Dolibaina, Dias & Zacca, sp. nov. and Z. warreni Dias, Zacca & Dolibaina, sp. nov. In addition, a neotype is designated for Satyrus pacarus Godart, [1824], and lectotypes are designated for Euptychia amalda Weymer, 1911, Euptychia fumata Butler, 1867 and Euptychia saundersii Butler, 1867.
The genus Microogenius Gutiérrez (Coleoptera: Scarabaeidae: Rutelinae: Rutelini), endemic to the Andean biogeographic region, is revised and now includes six species: Microogenius arrowi (Ohaus) (Bolivia), Microogenius borealis sp. nov. (Peru), Microogenius gutierrezi Martínez (Bolivia), Microogenius lanterii (Soula) (Argentina), Microogenius martinezi Gutiérrez (Bolivia) and Microogenius puna sp. nov. (Bolivia, Chile, Peru). Redescription of the genus, individual diagnoses, identification keys and distribution records for all known species are provided. Additionally, photographs of adults and of diagnostic morphological characters are included. Eremophygus calvus Gutiérrez, based on the female holotype, is synonymized under Microogenius arrowi (Ohaus), based on the male lectotype. The genus Microogenius is recorded for the first time for the altiplano of Chile and Peru based on specimens of a new species that has been long confused with Eremophygus lasiocalinus Ohaus.
Rhodopsin-based voltage imaging tools for use in muscles and neurons of Caenorhabditis elegans
(2019)
Genetically encoded voltage indicators (GEVIs) based on microbial rhodopsins utilize the voltage-sensitive fluorescence of all-trans retinal (ATR), while in electrochromic FRET (eFRET) sensors, donor fluorescence drops when the rhodopsin acts as depolarization-sensitive acceptor. In recent years, such tools have become widely used in mammalian cells but are less commonly used in invertebrate systems, mostly due to low fluorescence yields. We systematically assessed Arch(D95N), Archon, QuasAr, and the eFRET sensors MacQ-mCitrine and QuasAr-mOrange, in the nematode Caenorhabditis elegans ATR-bearing rhodopsins reported on voltage changes in body wall muscles (BWMs), in the pharynx, the feeding organ [where Arch(D95N) showed approximately 128% ΔF/F increase per 100 mV], and in neurons, integrating circuit activity. ATR fluorescence is very dim, yet, using the retinal analog dimethylaminoretinal, it was boosted 250-fold. eFRET sensors provided sensitivities of 45 to 78% ΔF/F per 100 mV, induced by BWM action potentials, and in pharyngeal muscle, measured in simultaneous optical and sharp electrode recordings, MacQ-mCitrine showed approximately 20% ΔF/F per 100 mV. All sensors reported differences in muscle depolarization induced by a voltage-gated Ca2+-channel mutant. Optogenetically evoked de- or hyperpolarization of motor neurons increased or eliminated action potential activity and caused a rise or drop in BWM sensor fluorescence. Finally, we analyzed voltage dynamics across the entire pharynx, showing uniform depolarization but compartmentalized repolarization of anterior and posterior parts. Our work establishes all-optical, noninvasive electrophysiology in live, intact C. elegans.
The genus Corambis Simon, 1901 includes five species; three of them, C. jacknicholsoni sp. nov., C. logunovi sp. nov. and C. pantherae sp. nov., are described here as new. The female of the C. foeldvarii Szűts, 2002 is described for the first time and a new generic diagnosis is proposed. The distribution and relationships of Corambis are discussed in terms of the geological and bioclimatic history of New Caledonia.