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Walter Biese described Littoridina santiagensis Biese, 1944 (Cochliopidae) from Estero Dehesa in 1944 based exclusively on external shell features and a second allopatric population in Yeso Spring three years later. Since 2011 different samplings have been carried out at the type locality and have only provided specimens of the morphologically similar invasive mudsnail Potamopyrgus antipodarum Gray, 1843 (Tateidae), raising doubts about the identity of the species. The recent finding of two snail morphotypes in Yeso Spring, a thick shelled form congruent with type specimens of L. santiagensis and a slender one morphologically associable to P. antipodarum, allowed comparative studies, including the taxonomic analysis of additional populations with similar shell morphology occurring in central Chile. A DNA barcoding (COI) approach identified the slender form from Yeso Spring in Maipo Basin and a second population from the contiguous Rapel Basin indeed as the invasive P. antipodarum; however, L. santiagensis was recovered among species of Potamolithus Pilsbry, 1896 (Tateidae), justifying the Potamolithus santiagensis (Biese, 1944) comb. nov. Besides recognition of three other populations as belonging to Potamolithus, the molecular analysis also suggests trans-Andean dispersal of this group of snails in the Southern Cone of South America.
The gigas species group of the subgenus Canthidium (Neocanthidium) is defi ned and described. This species group is composed of three described species [C. gigas Balthasar, 1939, Brazilian Atlantic Forest, including intrusions into Cerrado, C. bokermanni (Martínez et al., 1964), Chaco and western Cerrado in Brazil, Bolivia, Paraguay, and Argentina, and C. kelleri (Martínez et al., 1964), Brazilian Cerrado and neighbouring open areas] and three new species: Canthidium stofeli sp. nov. from the western and southern regions of the Brazilian Amazon, Canthidium feeri sp. nov. from French Guiana, and Canthidium ayri sp. nov. from the Brazilian Atlantic Forest. We present descriptions and redescriptions, illustrations, an identifi cation key and comments on the distributions of the species of the gigas group.
Virpazaria Gittenberger, 1969 is distributed in the Balkan Peninsula (Albania, Montenegro and Croatia) and inhabits the shallow subterranean habitat (MSS) on limestone base rock. Reviewing historical and recently collected material, two species, Virpazaria (Virpazaria) gittenbergeri Fehér & Erőss sp. nov. and Virpazaria (Virpazaria) pesici Fehér & Deli sp. nov., are introduced as new to science. The conservation status of the new species are assessed using IUCN criteria. Two taxa, Virpazaria (Virpazaria) pageti alexanderi Reischütz & Subai, 2012 and Virpazaria (Aemiliella) ripkeni pastorpueri Reischütz et al., 2011, are synonymized with their nominate subspecies. Some new distribution records, as well as geological and geomorphological data about the known locations for Virpazaria, are presented.
The Tallahatta Formation, Lisbon Formation, and Gosport Sand are the three lithostratigraphic units that make up the lower-to-middle Eocene Claiborne Group. In Alabama, these marine units are among the most fossiliferous in the state and a long history of scattered reports have attempted to document their fossil diversity. In this study, we examined 20 931 elasmobranch and bony fish elements, including otoliths, derived from Claiborne Group units in Alabama and identified 115 unequivocal taxa. Among the taxa identified, one new species is described, Carcharhinus mancinae sp. nov., and Pseudabdounia gen. nov. is a new genus erected to include two species formerly placed within Abdounia Capatta, 1980. New taxonomic combinations proposed include Pseudabdounia claibornensis (White, 1956) gen. et comb. nov., Pseudabdounia recticona (Winkler, 1874) gen. et comb. nov., Physogaleus alabamensis (Leriche, 1942) comb. nov., and Eutrichiurides plicidens (Arambourg, 1952) comb. nov. We also report the first North American paleobiogeographic occurrences of Aturobatis aff. A. aquensis Adnet, 2006, Brachycarcharias atlasi (Arambourg, 1952), Eutrichiurides plicidens comb. nov., Galeorhinus louisi Adnet & Cappetta, 2008, Ginglymostoma maroccanum Noubhani & Cappetta, 1997, Gymnosarda sp., Mennerotodus sp., Rhizoprionodon ganntourensis (Arambourg, 1952), Stenoscyllium aff. S. priemi Noubhani & Cappetta, 1997, Trichiurus oshosunensis White, 1926, and the first North American occurrence for a fossil member of the Balistidae Risso, 1810. Our sample also included 26 taxa that represented first paleobiogeographic occurrences for Alabama, including Abdounia beaugei (Arambourg, 1935), Albula eppsi White, 1931, Ariosoma nonsector Nolf & Stringer, 2003, Anisotremus? sp., Anomotodon sp., Brachycarcharias twiggsensis (Case, 1981), Burnhamia daviesi (Woodward, 1889), Eoplinthicus yazooensis Capetta & Stringer, 2002, Galeorhinus ypresiensis (Casier, 1946), Gnathophis meridies (Frizzell & Lamber, 1962), Haemulon? obliquus (Müller, 1999), Hypolophodon sylvestris (White, 1931), Malacanthus? sulcatus (Koken, 1888), Meridiania cf. M. convexa Case, 1994, Palaeocybium proosti (Storms, 1897), Paraconger sector (Koken, 1888), Paralbula aff. P. marylandica Blake, 1940, Phyllodus toliapicus Agassiz, 1844, Propristis schweinfurthi Dames, 1883, Pycnodus sp., Pythonichthys colei (Müller, 1999), Scomberomorus stormsi (Leriche, 1905), Signata stenzeli Frizzell & Dante, 1965, and Signata nicoli Frizzell & Dante, 1965, and the first Paleogene occurrences in Alabama of a member of the Gobiidae Cuvier, 1816. A biostratigraphic analysis of our sample showed stratigraphic range extensions for several taxa, including the first Bartonian occurrences of Eoplinthicus yazooensis, Jacquhermania duponti (Winkler, 1876), Meridiania cf. M. convexa, Phyllodus toliapicus, and “Rhinobatos” bruxelliensis (Jaekel, 1894), range extensions into the late Ypresian and Bartonian for Tethylamna dunni Cappetta & Case, 2016 and Scoliodon conecuhensis Cappetta & Case, 2016, the first late Ypresian records of Galeorhinus louisi, the first Lutetian occurrence of Gymnosarda Gill, 1862, and a range extension for Fisherichthys aff. F. folmeri Weems, 1999 into the middle Bartonian. Larger biostratigraphic and evolutionary trends are also documented, such as the acquisition of serrations in Otodus spp., possible population increases for the Rhinopterinae Jordan & Evermann, 1896 and Carcharhiniformes Compagno, 1973 in the Bartonian, and the apparent diversification of the Tetraodontiformes Berg, 1940 during the same stage. This study helps better our understanding of earlyto-middle Eocene elasmobranch and bony fish diversity, paleobiogeography, and biostratigraphy in the Gulf Coastal Plain of North America.
Neopanorpa van der Weele, 1909 is the second largest genus in Panorpidae, and over 170 Oriental species have been reported hitherto. In this paper, we describe two new species: Neopanorpa luojishana sp. nov. and Neopanorpa xingmini sp. nov. from Southwest China. We also report the first discovery of the male of Neopanorpa ocellaris (Navás, 1908) from Guangxi and Guizhou, China, a species recorded from Sikkim previously. Neopanorpa brevivalvae Chou & Wang, 1988 is synonymized with Neopanorpa lungtaushana Cheng, 1957. In addition, Neopanorpa furcula nom. nov. is proposed for Neopanorpa furcata Zhou, 2005, a junior homonym preoccupied by Neopanorpa furcata (Hardwicke, 1825). The biogeographical implications of some Neopanorpa species are discussed in brief.
There are 214 species of the suborder Tipulomorpha (Diptera) known from Panama. Of these, 162 species were described by the noted American entomologist, Charles Paul Alexander, from Panama during the period from 1912 through 1979. Panama hosts two of the four families found within the Tipulomorpha: Limoniidae (197 species) and Tipulidae (17 species). We have records of only three species from multiple provinces (n = 2) within Panama and 211 species from just one province. The vast majority of the latter are known from a single location within their respective provinces. There are 142 endemic species (66.4%) included in Panama’s Tipulomorpha fauna, with the remainder being found elsewhere in South America (48 species), Central America (44), Mexico (23 species), the Caribbean (14 species), and the United States (4 species). Whereas, this taxonomic group has benefited from collecting in the Canal Zone and the popular western highlands in Chiriqui Province, we know little or nothing of the distribution of species within the country, their natural history, or their relationship to water quality.
First records of Elachistinae are given from Thailand. Ten species of Elachistinae are reported, eight of which are described as new: Urodeta longa Sruoga & Kaila sp. nov., Elachista buszkoi Sruoga & Kaila sp. nov., E. oryx Sruoga & Kaila sp. nov., E. pellineni Sruoga & Kaila sp. nov., E. capricornis Sruoga & Kaila sp. nov., E. phichaiensis Sruoga & Kaila sp. nov., E. loeiensis Sruoga & Kaila sp. nov. and E. siamensis Sruoga & Kaila sp. nov. The new species are diagnosed and illustrated with photographs of the adults and genitalia. One species remains unidentified to species level.
In two separate occurrences, graduates of the Oregon Forest Pest Detector program discovered the exotic Agrilus cyanescens (Ratzeburg) (Coleoptera: Buprestidae) in Portland, Oregon, damaging a backyard shrub, Lonicera involucrata (Rich.) Banks ex Spreng. (Caprifoliaceae). Although first detected in the USA 99 years ago, the known occurrence nearest to Oregon is in Utah.
Jeekelosoma Mauriès, 1985, is upgraded from subgenus status under Eviulisoma Silvestri, 1910 to full genus status. The type species, Jeekelosoma abadi (Mauriès, 1985) is redescribed based on topotypical material from a cave in Morocco. Jeekelosoma heptarachne sp. nov. and J. viginti sp. nov. are described from two further Moroccan caves.
The new Southeast Asian genus Cambonilla gen. nov. (Zodariidae, Araneae): 'bis repetita placent'
(2019)
The new genus Cambonilla Jocqué gen. nov. is described on the base of two species, each known from both sexes. A cladistic analysis based on morphology, showed that the new genus is the sister-group of Heliconilla Dankittipakul, Jocqué & Singtripop, 2012 with which it shares the granulated carapace with branched setae and the marbled ventral abdominal pattern, but differs by the abdominal, tubular sclerotized protrusion around the pedicel in males and the absence of posterior ventral abdominal spines in the female. The type species Cambonilla securicula Jocqué gen. et sp. nov. was found in rainforest along the Mekong River in Cambodia and Laos. The second species Cambonilla symphonia Jocqué & Henrard gen. et sp. nov., provided with conspicuous femoral stridulating organs, was recorded from the same localities but in Cambodia only. An illustrated key to the genera of tropical Asia is presented.
Coronuloid barnacles are epibionts of several marine vertebrates (including cetaceans and sea turtles) as well as invertebrates, and are assigned to two families of turtle barnacles (Chelonibiidae Pilsbry, 1916 and Platylepadidae Newman & Ross, 1976) and one family of whale barnacles (Coronulidae Leach, 1817). Chelonibiids and coronulids have a scanty, albeit significant fossil record extending back to the Eocene and Pliocene, respectively; in turn, the fossil record of platylepadids is limited to a single record from the Upper Pleistocene. Here we report on an isolated carinolateral compartment of Platylepas Gray, 1825, the type genus of the family, from Lower Pleistocene (Gelasian) epibathyal deposits exposed at Milazzo (Sicily, Italy). This specimen is here designated holotype of a new species, †Platylepas mediterranea sp. nov. We argue that, like most extant members of Platylepas, †P. mediterranea sp. nov. lived partially embedded in the skin of a sea turtle. This record of an extinct platylepadid – the first from the Mediterranean region and the second worldwide – pushes back the fossil record of Platylepadidae to the lowermost Quaternary, thus possibly supporting an even earlier (e.g., Neogene) timing for the origin of this family and adding a new chapter to the evolutionary history of one of the most diverse and successful lineages of epizoic crustaceans.
The Palearctic flea beetle Epitrix pubescens (Koch) (Coleoptera: Chrysomelidae: Galerucinae: Alticini) is reported as established in North America. It is recorded in the United States from Illinois, Massachusetts, New Hampshire, New York, Oregon, and Wisconsin, and in Canada from the Provinces of Nova Scotia, Ontario, and Quebec. The oldest records are from 1975. The species has been reported feeding on Solanum dulcamara L. (Solanaceae). Full distributional information and reference photos for identification are provided. Epitrix pubescens may have avoided detection for such a long time due to its size, difficulty of identification, and affinity for a weed rather than agricultural crops. The more than 40-year lag between arrival and discovery of an immigrant species illustrates the importance of routine biodiversity monitoring efforts and taxonomic works.
Eleven species of Ctenopelma Holmgren, 1857 are reported from China. Five species are new to science: C. labiatum Sheng, Sun & Li sp. nov., from Ningxia Hui Autonomous Region, C. lii Sheng, Sun & Li sp. nov., from Liaoning province, C. rufofasciatum Sheng, Sun & Li sp. nov., reared from Cephalcia lariciphila (Wachtl, 1898) from Beijing, C. pineatum Sheng, Sun & Li sp. nov., reared from Acantholyda posticalis (Matsumura, 1912) and Cephalcia lariciphila from Beijing and Henan, Shanxi, Shan’xi, Liaoning, Jilin and Heilongjiang provinces, and C. spiraculare Sheng, Sun & Li sp. nov., reared from Cephalcia lariciphila from Henan and Shanxi provinces. One species, C. nigrum Holmgren, 1857, reared from Cephalcia lariciphila in Beijing, is a new record for China. Ctenopelma tomentosum (Desvignes, 1856) was reared from Neurotoma sibirica Gussakovskij, 1935 (new host record) in Liaoning province. A key to species of Ctenopelma known in China is provided.
A total of nine families of Trichoptera were identified from material collected in Malaise and light traps in the western part of Nyungwe National Park, southwestern Rwanda, late October 2018. Included in the material was an undescribed species of Pisuliidae which is described herein as Silvatares laetae Ngirinshuti & Johanson sp. nov. The new species adds to the six Pisuliidae species previously recorded for the East African region, five endemic to Tanzania and one to Uganda. This study portrays the first results of an ongoing survey on the Trichoptera fauna of Rwanda.
The Quebrada Rambala drainage is found immediately south and south-southeast of the town of Chiriqui Grande and east of Rambala on the Caribbean coast. It is one of two tributaries of the Rio Margarita watershed, a small, lowland drainage with elevations up to 180 m. During the 2014-2017 period, collections of caddisflies (Insecta: Trichoptera), employing both UV-light and Malaise traps, were made at two locations on Quebrada Rambala proper, and four locations on its unnamed tributary, all on a land area of approximately 1 ha. As a result, 127 species of caddisflies were identified, including 59 species of microcaddisflies. A non-parametric estimator of true, or potential, species richness based on rare species present for this watershed is 211 species. Previously, 19 new country records were published from this location. In this paper, we record three additional country records (Hydrobiosidae: Atopsyche minimajada Blahnik and Gottschalk; Hydroptilidae: Leucotrichia rhomba Thomson and Holzenthal and Oxyethira (Oxytrichia) apinolada Holzenthal and Harris) and describe and illustrate 19 new species of microcaddisflies (Alistotrichia bernali, Cerasmatrichia blahniki, Costatrichia santosi, Metrichia macdonaldi, M. thomsonae, M. thurmani, M. trebeki, Neotrichia carlsoni, N. rambala, N. serrata, N. starki, Ochrotrichia birdae, O. dewalti, O. kondratieffi, Oxyethira buenoi, Rhyacopsyche holzenthali, Tizatetrichia panamensis, Zumatrichia flinti, and Z. hazelae). Combined, this one small portion of the Quebrada Rambala has increased Panama’s caddisfly fauna by 41 species of microcaddisflies. Additionally, several new species of macrocaddisflies await description. Finally, we add one new genus to Panama’s fauna (Hydroptilidae: Tizatetrichia Harris, Flint, and Holzenthal). With the publication of these new taxa, Panama’s caddisfly fauna now includes 403 species in 15 families and 53 genera. We also suggest that multiple collections over time for all stream orders, employing several collection methods, are required in order to better estimate species richness within a drainage.
Herein we describe three new species of Smicridea McLachlan (S. (S.) lata, S. (S.) spatulata, and S. (S.) dividua) from Panama in the nigripennis species group (Trichoptera: Hydropsychidae). The nigripennis species group is characterized by having a rather complex phallic apparatus, open anteroventrally and posterodorsally, with ventral and lateral portions produced into lobes, and with spines and other structures arising from the endothecal membranes. All three species resulted from a 2017 survey of Omar Torrijos and Santa Fe National Parks. Twenty-six species of Smicridea, nine of them endemic, are now known from Panama.
Herein we describe five new species in the trichopteran family Glossosomatidae Wallengren (Insecta: Trichoptera) from Panama: Mortoniella calovebora Blahnik and Armitage, n. sp., M. yayas Blahnik and Armitage, n. sp., Protoptila inflata Blahnik and Armitage, n. sp., P. totumas Blahnik and Armitage, n. sp., and P. rambala Blahnik and Armitage, n. sp. Three of the species were collected as part of ongoing biological surveys of Panama’s national parks. We also record three new country records for Panama for this family: Culoptila costaricensis Flint, 1974, Mortoniella opinionis Blahnik and Holzenthal, 2008, and Protoptila spirifera Flint, 1974. Thirty-one species of glossosomatid caddisflies, nine of them endemic, are now known from Panama.
Atelopus is a species-rich group of Neotropical bufonids. Present knowledge on bioacoustics in this genus is relatively poor, as vocalisations have been described in only about one fifth of the ca. 100 species known. All studied members of the genus produce vocalisations although, with a few exceptions, most species lack a middle ear. Nonetheless, hearing has been demonstrated even in earless Atelopus making bioacoustics in these toads an inspiring research field. So far, three structural call types have been identified in the genus. As sympatry is uncommon in Atelopus, calls of the same type often vary little between species. Based on recordings from the 1980s, we describe vocalisations of three Venezuelan species (A. carbonerensis, A. mucubajiensis, A. tamaense) from the Cordillera de Mérida, commonly known as the Andes of Venezuela and the Tamá Massif, a Venezuelan spur of the Colombian Cordillera Oriental. Vocalisations correspond, in part, to the previously identified call types in Atelopus. Evaluation of the vocalisations of the three species presented in this study leads us to recognise a fourth structural call type for the genus. With this new addition, the Atelopus acoustic repertoire now includes (1) pulsed calls, (2) pure tone calls, (3) pulsed short calls and (4) pure tone short calls. The call descriptions provided here are valuable contributions to the bioacoustics of these Venezuelan Atelopus species, since all of them have experienced dramatic population declines that limit possibilities of further studies.
Thopeutica (Thopeutica) petertaylori Medina, Cabras and Wiesner (Coleoptera: Cicindelidae), new species, is described from the Cagan river, New Bataan, Mindanao. It is characterized by the metallic ground colour of the elytra, prominent middle tooth in the labrum, and bottle-shaped aedeagus with apical hook.