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Cylindera (Cylinderina) sierramadrensis Wiesner and Dheurle, new species (Coleoptera: Cicindelidae) is described from Luzon. Re-descriptions of the other seven species of this subgenus (C. (C.) nanula (Horn, 1937), C. (C.) nana (Schaum, 1862), C. (C.) pseudonana (Horn, 1924), C. (C.) werneri Wiesner, 1988, C. (C.) rothschildi (Horn, 1896), C. (C.) genieri Cassola and Werner, 2003, C. (C.) vandenberghei Dheurle, 2016) are provided together with a key and pictures of their habitus, labrum and aedeagus.
Adults of the Neotropical genera Beltia Jacoby (type species: Beltia nicaraguensis Jacoby) and Colaspoides Laporte (type species: Colaspoides limbata [Olivier]) (Chrysomelidae: Eumolpinae: Eumolpini) are difficult to separate. In this paper, the genus Beltia Jacoby is redefined and diagnosed by features of the pygidium, lateral wings of the prosternum, and metatibiae to distinguish it from Colaspoides and other medium-sized, ovate Eumolpini. Fourteen new species from Costa Rica, Panama, Colombia, Ecuador, and Peru are described and illustrated—Beltia awapita, B. confusa, B. gorgona, B. herreri, B. ledesmae, B. napoensis, B. osa, B. rugosa, B. sanchezae, B. talaga, B. tilarana, B. tisingalita, B. tsachila and B. vacilona. A key and range maps for all species recognized herein are provided. Colaspoides placidula Bechyne, Colaspoides placidula angustomarginata Bechyne, Colaspoides chiriquensis Jacoby, and Colaspoides weyrauchi Bechyne are transferred to Beltia and redescribed. Colaspoides turrialbana Bechyne is synonymized with B. chiriquensis, and Colaspoides chanchamaya Bechyne is synonomized with B. weyrauchi. Morphological similarities with Beltia indicate that Old World Colaspoides also should be removed from Colaspoides s. str.
The life history of Enaphalodes archboldi Lingafelter and Chemsak (Coleoptera: Cerambycidae) is described in detail based on observations from Marion County, Florida. Notes on the life history of Enaphalodes bingkirki Lingafelter and Santos-Silva from Honduras are also provided. Enaphalodes bingkirki is reported from Honduras for the first time.
Euryuridae Pocock 1909 and Eurymerodesmidae Causey 1951, both endemic to the eastern/central United States (US), are incorporated into Xystodesmidae Cook 1895 and reduced to subfamilies and (sub)tribes n. stats. Euryurina and Melaphina Brolemann 1916, n. stats., are sister-taxa that differ primarily in epiproctal configurations and comprise Euryurini; sister-taxa Eurymerodesmina and Nannariina Hoffman 1964, n. stats., the latter transferred from Xystodesminae, comprise Eurymerodesmini, n. stat., in which plesiomorphic forms exhibit sublinear, "stick-like," and subapically curved/bent gonopodal acropodites with moderately-long to long hairs, often with distal tufts, on their “inner” surfaces. Additional transferrals include Wamokia Chamberlin from the xystodesmine tribe Xystocheirini to Xystodesmini (= Harpaphini), and Macellolophus Attems, from Xystodesmidae to Chelodesmidae. Except for Chonaphini, the term, "prefemoral process," has traditionally been assigned to the secondary and shorter telopodital projection regardless of its position, origin, or configuration. Homology of these different structures has never been demonstrated and requires investigation, but the multitude of differences suggests that they are not such and warrant different names, for example "femoral process," for the similarly positioned branches in Devillea Brölemann and Rhysodesmus Cook (Xystodesminae: Devilleini, Rhysodesmini). The latter tribe may be polyphyletic, and new tribes may be required for components with acicular "prefemoral processes" (Boraria and Cherokia, both by Chamberlin, Gyalostethus and Erdelyia, both by Hoffman, and Pleuroloma Rafinesque) and the southeastern US genera with small-bodied species (Caralinda Hoffman and Gonoessa, Parvulodesmus, and Lourdesia, all by Shelley). Taxonomic value is accorded the "prefemoral extension/elongation," which is absent from Eurymerodesmina; complete, encircles the acropodite, and extends for ~1/3 to 1/2 of the latter’s lengths in Euryurini; and incomplete and extends for ~1/4 to 1/3 of the "outer" acropodital surfaces in Nannariina and xystodesmine tribes. Other newly recognized taxonomic characters include the "inner" and "outer" acropodital surfaces/margins, the position on the acropodital stem of the "distal curve/bend," and the length of the "distal zone." Rhysodesmus and Sigmoria (Rudiloria) t. trimaculata (Wood) (Xystodesminae: Rhysodesmini, Apheloriini) are recorded from, respectively, Chihuahua, Mexico, and Québec, Canada, as are Xystodesmidae/-inae and, provisionally, Chonaphini, Montaphe Chamberlin, and M. elrodi (Chamberlin), the only plausible taxa for an unidentifiable juvenile from near Yahk and only 2.5 km (1.6 mi) north of the International Border. The southern periphery of interior British Columbia (BC) thus represents the second xystodesmid faunal region in BC and the third in Canada. While incorporation of Euryuridae does not affect the family’s overall distribution, that of Eurymerodesmidae fundamentally alters it by joining the formerly separate East-Nearctic and Meso-American regions into a continuous one extending, north-south, from Montréal Island, Québec, to Santa Ana Department, El Salvador, a distance of around 4,944 km (3,090 mi). Xystodesmidae also inhabit two West-Nearctic regions, one in the interior stretching from southernmost BC to northeastern Oregon and the other running along the Pacific Coast from southern Alaska to southern California. The family also occupies two Palearctic regions, each with three subregions, an eastern one spreading from Hokkaido, Japan, and the southern Maritime Province, Russia, to Taiwan; a point locality in northern Vietnam; and southern/eastern China. The second Palearctic area extends along the Mediterranean and adjoining seas from Morocco, Sardinia, and the southeastern corner of France to Cyprus and southern coastal Turkey. New locality data, references, and maps are provided along with diagnostic accounts of all reconceptualized taxa and new/revived statuses.
A simple, sublinear, "stick-like" acropodite with a curve or bend near midlength or subapically and without a secondary telopodital projection is the hypothesized plesiomorphic gonopodal condition in Xystodesmidae. This form has undergone multitudinous modifications/alterations - twists, curls, variably configured thickened and laminate expansions, reductions, bi-/trifurcations, enlargements, ornamentations, etc. that are manifested in today’s xystodesmine tribes. When Avalonia collided with Baltica 450 million years ago, ancestral xystodesmoideans on the former dispersed into the latter, penetrated and occupied vacant niches, and evolved into today’s Melaphina (Euryurinae: Euryurini) and Devilleina (Xystodesminae). A similar evolutionary burst leading to today’s Nearctic and East-Palearctic faunas occurred 10 million years later when Avalonia + Baltica collided with Laurentia to form Euramerica. Ancestral forms of Euryurinae and Xystodesminae again penetrated vacant niches and evolved; the former maintained the general gonopodal structural pattern of Melaphina but changed the epiproct from triangular to broad and spatulate, thereby creating Euryurina. The earliest xystodesmine taxa to evolve in Laurentia were Rhysodesmini and Rhysodesmus, which spread southwestward, penetrated "proto- Mexico, and left relict populations in today’s southern Appalachians. Eurymerodesmina and Nannariina arose from ancestral euryurine stock prior to the Cretaceous in western Appalachia in their present area of overlap. The former dispersed to the west and south while the latter expanded to the east and north; consequently, the Western Inland Seaway minimally impacted Nannariina while eradicating Eurymerodesmina from the inundated area. Today’s populations in the Plains and south-southeastern states therefore represent secondary dispersion in the past 50-60 million years. The Seaway also eradicated Rhysodesmus from these areas, but enough forms survived in high mountain refugia to replenish the fauna when the embayment receded.
The species Canthidium alvarezi Martínez and Halffter, 1986 (Coleoptera: Scarabaeidae: Scarabaeinae) is transferred to the genus Ateuchus Weber, 1801, becoming Ateuchus alvarezi (Martínez and Halffter), new combination. Its relationship with other species in the genus is briefly discussed. The validity and ranking of the genus Lobidion Génier, 2010, originally described from a single female, is discussed based on the discovery of male specimens, which lead us to reclassify it as a monotypic subgenus of Ateuchus, becoming Ateuchus (Lobidion), new rank, with the only included species becoming Ateuchus (Lobidion) punctatissimus (Génier, 2010) new combination.
Nomenclatural changes are proposed and herein implemented for several beetles in the family Lampyridae (Coleoptera). Corrections of authorship are proposed for Psilocladus marginatus (Lewis), Psilocladus ruficollis (Kiesenwetter), and Dryptelytra fulvipennis E. Olivier. Dates of publication are corrected for Magnoculus marginatus (Guérin-Méneville), Psilocladus calvus Kirsch, Psilocladus peruvianus Kirsch, and Vesta vitellinothorax (Perty) a synonym of Vesta thoracica (G. A. Olivier). "Dodacles grandjeani E. Olivier" is found to be a nomen nudum, which actually refers to Dryptelytra grandjeani (E. Olivier).
The males of Caraphia squamosa (Chemsak and Linsley, 1984) and C. seriata (Chemsak and Linsley, 1984), and the female of C. lingafelteri Ohbayashi and Yamasako, 2016 (Coleoptera: Cerambycidae: Lepturinae) are described for the first time. Two new Caraphia species are described: C. warneri Wappes and Santos-Silva, from Guatemala; and C. woodruffi Wappes and Santos-Silva, from Guatemala and Honduras. A key to American species of Caraphia and a map showing their known distribution is provided. New country records for C. seriata and C. lingafelteri are also provided. Lastly, the C. seriata record for Honduras was based on specimens of a new species (Caraphia lingafelteri), hence the Honduras record should be deleted.
The following nomenclatural changes for several firefly taxa (Coleoptera: Lampyridae) are proposed and herein implemented. Correction of authorship is proposed for Lampyroidea lucifer (Reiche and de Saulcy, 1857). Spelling corrections are proposed for Photinus coroicosus Pic, 1941 and Macrolampis flavithorax Pic, 1940. Dates of publication are corrected for Photinus curticornis Pic, 1940, Phausis riversi (LeConte, 1885), Ellychnia autumnalis Melsheimer, 1846, Ellychnia facula LeConte, 1854, Lamprigera nitidicollis (Fairmaire, 1891), Cladodes gloriosus E. Olivier, 1909, Photuris brunnipennis Jacquelin Du Val, 1857, Pyrogaster subnitidus Pic, 1928, Pyrogaster telephorinus (Perty, 1830), and Lampyroidea dispar (Fairmaire, 1857).