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A revision of the genus Asterostegus Mortensen, 1933 (Echinodermata: Ophiuroidea: Euryalidae) is based on seven specimens, including the holotype of Asterostegus maini McKnight, 2003. A new species, Asterostegus sabineae sp. nov., is described from off Reunion Island and two other species, A. tuberculatus Mortensen, 1933 and A. maini, are redescribed. A tabular key to the three species of the genus Asterostegus is provided. Some terminology of the taxonomy of euryalid ophiuroids is revised.
The types of nominal species of Diapriinae in the collection of the Natural History Museum, London, are catalogued. Lectotypes are designated for the following taxa: Diapria peraffinis Ashmead, 1896; D. smithii Ashmead, 1896; Galesus bipunctatus Ashmead,1894; G. (G.) foersteri var. nigricornis Kieffer, 1911; G. sexpunctatus Ashmead, 1893; G. walkeri Kieffer, 1907; Idiotypa nigriceps Kieffer, 1909; I. nigriceps Kieffer, 1911; I. pallida Ashmead, 1893; I. pallida Ashmead in Riley, Ashmead & Howard, 1894; Paramesius angustipennis Kieffer, 1911; P. cameroni Kieffer, 1911; Phaenopria cameroni Kieffer, 1911; P. halterata Kieffer, 1911; P. magniclavata Ashmead, 1896; Tropidopsis clavata Ashmead, 1893; T. clavata Ashmead in Riley, Ashmead & Howard, 1894. New combinations are proposed: Aneuropria bifurcata comb. nov. for Mantara bifurcata Dodd, 1920; Basalys quadridens comb. nov. for Microgalesus quadridens Kieffer, 1912; Coptera cratocerus comb. nov. for Galesus cratocerus Cameron, 1912; Coptera sexpunctata comb. nov. for Galesus sexpunctatus Ashmead, 1893; Doliopria magniclavata comb. nov. for Phaenopria magniclavata Ashmead, 1896; Spilomicrus aterrimus comb. nov. for Hoplopria aterrima Dodd,
1920; Spilomicrus campbellanus comb. nov. for Antarctopria campbellana Yoshimoto, 1964; Spilomicrus coelopae comb. nov. for Antarctopria coelopae Early, 1978; Spilomicrus diomedeae comb. nov. for Antarctopria diomedeae Early, 1978; Spilomicrus helosciomyzae comb. nov. for Malvina helosciomyzae Early & Horning, 1978; Spilomicrus insulae comb. nov. for Malvina insulae Early, 1980; Spilomicrus latigaster comb. nov. for Antarctopria latigaster Brues in Tillyard, 1920; Spilomicrus punctatus comb. nov. for Malvina punctata Cameron, 1889; Spilomicrus rekohua comb. nov. for Antarctopria rekohua Early, 1978; Trichopria bouceki comb. nov. for Oxypria bouceki Masner, 1959; Trichopria nigriceps comb. nov. for Tropidopria nigriceps Ashmead in Riley, Ashmead & Howard, 1894; Trichopria nigriceps comb. nov. for Xyalopria nigriceps Kieffer, 1907; Trichopria spinosiceps comb. nov. for Acidopria spinosiceps Dodd, 1920; Trichopria walkeri comb. nov. for Diapria walkeri Dalla Torre, 1890. New replacement names are proposed: Coptera mosselensis nom. nov. for C. nigricornis Nixon, 1930 preocc.; Coptera pijiguaorum nom. nov. for C. sexpunctata Montilla & García, 2008 preocc.; Spilomicrus kozlovi nom. nov. for S. punctatus Kozlov, 1978 preocc.; Trichopria fluminis nom. nov. for T. nigriceps (Kieffer, 1907) preocc.; T. thermarum nom. nov. for T. nigriceps (Kieffer, 1913) preocc. New specific synonyms are proposed: Basalys cursitans (Kieffer, 1911) = B. pedisequa (Kieffer, 1911) syn. nov. (the former removed from synonymy with B. parvus Thomson, 1858); B. iphicla Nixon, 1980 = B. macroptera (Kieffer, 1911) syn. nov.; Coptera bipunctata (Ashmead in Riley, Ashmead & Howard, 1894) = C. sexpunctata (Ashmead, 1893) syn. nov.; Idiotypa nigriceps Kieffer, 1911 = I. nigriceps Kieffer, 1909 syn. nov.; I. pallida Ashmead in Riley, Ashmead & Howard, 1894 = I. pallida Ashmead, 1893 syn. nov.; Psilus nigricornis (Kieffer, 1911) = P. fuscipennis (Curtis, 1831) syn. nov.; P. walkeri (Kieffer, 1907) = P. fuscipennis (Curtis, 1831) syn. nov.; T. bouceki (Masner, 1959) = T. conotoma (Kieffer, 1911) syn. nov.; Trichopria halterata (Kieffer, 1911) = T. halterata (Kieffer, 1909) syn. nov. New generic synonyms are proposed: Antarctopria Brues in Tillyard, 1920 = Spilomicrus Westwood, 1832 syn. nov.; Malvina Cameron, 1889 = Spilomicrus Westwood, 1832 syn. nov.; Mantara Dodd, 1920 = Aneuropria Kieffer, 1905 syn. nov.; Microgalesus Kieffer, 1912 = Basalys Westwood, 1833 syn. nov.; Xyalopria Kieffer, 1907 = Trichopria Ashmead, 1893 syn. nov. (Xyalopria is removed from synonymy with Megaplastopria Ashmead, 1903). A brief account of some aspects of the history of these types is given.
Three fossil leafhopper inclusions from Eocene Baltic amber, representing three new extinct genera and species, are described and illustrated. Eomegophthalmus lithuaniensis gen. et sp. nov. is tentatively placed in Megophthalminae, although it may represent the stem group from which Megophthalminae, Ulopinae, and Membracidae arose. Xestocephalites balticus gen. et sp. nov. and Brevaphrodella nigra gen. et sp. nov. are placed in Aphrodinae: Xestocephalini based on the structure of the head, leg chaetotaxy, and male genital capsule. These new genera and species represent the oldest known representatives of their respective subfamilies and the latter is the oldest known brachypterous adult leafhopper.
The study of the Portuguese marine ichthyofauna has a long historical tradition, rooted back in the 18th Century. Here we present an annotated checklist of the marine fishes from Portuguese waters, including the area encompassed by the proposed extension of the Portuguese continental shelf and the Economic Exclusive Zone (EEZ). The list is based on historical literature records and taxon occurrence data obtained from natural history collections, together with new revisions and occurrences. It comprises a total of 1191 species, distributed among 3 superclasses, 4 classes, 42 orders, 212 families and 617 genera. If considering only the EEZ and present territorial waters, this list represents an increase of 230 species (27.8%) and of 238 species (29.0%), when compared to the information available in FishBase (2012) and in the last checklist of marine and estuarine fishes of Portugal (1993), respectively. The order Perciformes shows the highest diversity, with 54 families, 162 genera and 299 species. Stomiidae (80 species), Myctophidae (71 species) and Macrouridae (37 species) are the richest families. From the listed species, 734 are present off mainland Portugal, 857 off the Azores and 766 off Madeira. Within the limits of the examined area, three species are reported for the first time in mainland Portugal and twenty-nine records are identified as doubtful. A total of 133 species have been recorded from the extended Portuguese continental shelf (2 off mainland Portugal, 117 off the Azores and 14 off Madeira), two of which are common to the Azores and Madeira extensions. Biogeographically, the Atlantic group is the most important (548 species – 46.01%), followed by the Lusitanian group (256 species – 21.49%), the African group (71 species – 5.96%), the Boreal group (34 species – 2.85%), the Mediterranean group (31 species – 2.60%), the Macaronesian group (21 species – 1.76%), the Atlantic/African group (19 species – 1.60%) and the Mediterranean/African and the Arctic groups, each with only 1 species (0.08%). Regarding the preferences for vertical habitat, the demersal fishes are the most important group (305 species – 25.61%), followed by the mesopelagic group (228 species – 19.14%), the bathypelagic group (164 species – 13.77%), the benthopelagic group (147 species – 12.34%), the bathydemersal group (115 species – 9.66%), the reef-associated group (88 species – 7.39%), the pelagic group (74 species – 6.21%), the epipelagic group (58 species – 4.87%) and 1 species (0.08%) of the benthic group. The oceanic habitat is the best represented group comprising 446 species (37.45%), followed by the shelf group (199 species – 16.71%), the slope group (164 species – 13.77%), the inner shelf group (89 species – 7.47%), the coastal group (70 species – 5.88%), the outer shelf group (29 species – 2.43%) and the oceanic/shelf group (7 species – 0.59%).
For the first time Amphipoda have been discovered living in Bryozoa. A new genus and species of the amphipod family Chevaliidae, Bryoconversor tutus gen. et sp. nov. is described from New Zealand at depths of 530–1500 m. The species lives in an inquiline relationship with the cheilostome bryozoan Onchoporoides moseleyi (Calwelliidae), inhabiting an abfrontal basal coelom of the bryozoan beneath the membranous ectocyst (cuticularized epithelium) that conceals and protects the amphipods. The colony is strengthened along all edges by a unique intracoelomic rod of calcium carbonate that is formed within the marginal kenozooids of the colony. The potential benefits and costs to the bryozoan are discussed.
In this article, the author shows that progress of info-communications is a key factor of society changes, as it radically changes the key aspects of human life. Studying the time of progress and comparing it with the most important anthropic characteristic - length of human life, he comes to the conclusion that our generation has witnessed the tipping point in the rate of development of human civilization. This showing up in the fact that the present stage of the scientific and technological advance lead to the transformation, perhaps on the same scale, what were the appearance of written language and publishing, but these multiple fundamental changes in the life of society occur within the life of a single generation. In these circumstances, the task of forecasting, in its traditional setting, is becoming increasingly inaccurate. According to the author, the only possibility is to venture outside the framework of formal logic and technocratic approaches and try to find answers to these questions by generating new meanings of the realities surrounding us and in this context philosophy has a special role.
In der Hindu Tradition zeigen sich zwei grundsätzlich unterschiedliche Strömungen. Einmal gibt es die Richtungen, die sich die Befreiung vom Joch des durch das eigene Werk, Karma, bestimmten Rads der Wiedergeburten, Samsara, aufs Panier geschrieben haben. Zum anderen gibt es die karmistische Religion, die genau das eigene Werk zum entscheidenden, wenn nicht gar alleinigen Kriterium menschlicher Existenz erhebt. Diese karmistische Religion bildete und bildet den geistigen Hintergrund der indo-asiatischen Kultur so sehr, daß sich ihre Gegner immer noch vor ihr rechtfertigen müssen. Während die karmistische Existenzdeutung besonders unter den Buddhisten und Jainas in voller Blüte steht, haben die großen Religionen der Shaivas, Vaishnavas und Shaktas schon früh in ihren zahllosen Bewegungen massiv gegen den Karmismus Front gemacht. Dennoch gilt die Karma-Samsara-Lehre als Beschreibung des Normalfalls der Existenzgestaltung. Die ist die stets vorausgesetzte Mechanik des Existenzprozesses. Aber als ein unaufhebbares Schicksal wird sie nicht mehr so ohne Weiters im Hindutum anerkannt. Die o.g. Bewegungen sind denn auch religiöse Revolten, die auf höchst unterschiedliche Weise gegen die absolute und allgemeine Geltung der Karma-Samsara-Lehre durchaus erfolgreich Widerstand leisten. Wie in den anderen Kulturen auch ist der Kampf zwischen beiden Religionen im Hindutum das zentrale Thema der geistigen Auseinandersetzung mit der eigenen Existenz. Diese so konträre Sichtsweisen der Existenz im Hindutum, d.h. die karmistische und antikarmistische Religion, sollen im Folgenden an je einem Fallbeispiel aus noch immer gültigen heiligen Schriften vorgestellt werden.