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Yin und Yang im Klassenzimmer? : China-Moden der 80er Jahre – mit einem kurzen Rückblick auf Brecht
(1985)
In zwei Beiträgen der Zeitschrift Diskussion Deutsch (Heft 84/1985) wurde ein Denkmodell ins Licht der Diskussion gestellt, das bis dahin eher in kleinen Zirkeln sich verborgen hatte: die Sucht, Rettung beim >Uralten< zu finden. Es war nicht, wie bei gestandenen Konservativen, das >Klassische<, es waren nicht >die Alten<, nein, das UR-Alte musste es sein, nämlich die Geheimnisse des Fernen Ostens, das Tao und Yin und Yang. Nun, zwanzig Jahre später, sind Tai Chi, Qi Gong, Bachblüten, Gaia, Heilenergien, Rebirthing, Reiki, Karmaarbeit etc. pp. zum esoterischen Alltag bzw. ist Esoterik alltäglich geworden. Das war ein Anlass, diese Miszelle wieder hervorzuholen, die damals – offensichtlich vergeblich – versuchte, jenes Denkmodell ins Licht der Kritik und damit in seiner Unreflektiertheit bloß zu stellen: westliches Denken spiegelt hier das Licht des Ostens gleichsam blind, nämlich ohne es zu reflektieren.
The influence and power of some OECD states is under threat but China appears to remain astonishingly flexible, economically potent, and politically strong. How accurate is this view? To answer this question, major aspects of Chinese economic regulation that were adopted in the country’s progress towards capitalist modernization are examined. The analysis requires a historical reconstruction of how China changed the way it intervenes economically and politically, especially with regard to the institutions of the central state. Such a reconstruction reveals that, since the 1990s, the central state has indeed increased its steering capacities. These capacities have a distinctive basis that includes acceptance of a state-centered approach, idiosyncratic innovation policies taking place in the "shadow" of the state’s hierarchy, and the ongoing influence of the communist party. An all-embracing controlling power is, however, not detectable. What does exist in China’s competition-driven system of “statecapitalist” regulation, is a set of limits on the state’s capacity to govern.
Here, I describe four new species of the Neoserica vulpes species group: Neoserica daxue sp. nov., N. mianningana sp. nov., N. myanmarensis sp. nov., and N. yanyuan sp. nov. Genitalia and habitus of the new species are illustrated. Additional records of species from the group are given and the key to species of the Neoserica vulpes species group is updated.
Three new species of the genus Guiodytes Tian, 2013 are described from the limestone caves of Guangxi Zhuang Autonomous Region, southern China: Guiodytes weii Huang & Faille sp. nov. and Guiodytes yueliangensis Huang & Tian sp. nov. from Dapo Dong and Huang Dong caves, respectively, in Huanjiang County, northernmost Guangxi; Guiodytes inexpectatus Tian & Zhou sp. nov. from the Zhuzhu Dong cave in Longzhou County, southwestern Guangxi. All of the six known species of Guiodytes are endemic to Guangxi, ranging from the southwest to the northernmost. A modified key to species and a distribution map for Guiodytes are provided.
Three new species of Patrus Aubé, 1838 are described from China: Patrus hainanensis sp. nov. from Hainan; Patrus jiangxiensis sp. nov. from Jiangxi; Patrus shangchuanensis sp. nov. from Guangdong. Eight species / subspecies of Gyrinidae are recorded from China for the first time: Metagyrinus vitalisi (Peschet, 1923), Orectochilus argenteolimbatus Peschet, 1923, Orectochilus murinus Régimbart, 1892, Patrus haemorrhous (Régimbart, 1892), Patrus marginepennis angustilimbus (Ochs, 1925) from Yunnan; Patrus coomani (Peschet, 1925) from Guangdong; Patrus procerus (Régimbart, 1884) from Guangxi; Patrus annandalei (Ochs, 1925) from Hainan. Additional faunistic data of Gyrinidae from China are provided. A key to Chinese species of Patrus Aubé based on examined specimens from China is given.
This paper deals with the brachypterous Meconematini, including three new genera, Acosmetides gen. nov., Neocyrtopsides gen. nov. and Macrocosmetura gen. nov. Five new species are described: Acosmetides peltates gen. et sp. nov., Acosmetides dilobosa gen. et sp. nov., Acosmetides platycerca gen. et sp. nov., Neocyrtopsides bispina gen. et sp. nov. and Macrocosmetura truncata gen. et sp. nov. Two new combinations are proposed: Acosmetides trigentis (Wang, Bian & Shi, 2016) gen. et comb. nov. and Neocyrtopsides platycata (Shi & Zheng, 1994) gen. et comb. nov.
Glyptostrobus Endlicher is well represented in early Early Cretaceous to Pleistocene deposits in the middle to high latitudes of North America and Eurasia. Although the taxonomy and nomenclature of the genus is complicated, the fossil record indicates Glyptostrobus was represented by a small number of species. The genus first appears in Aptian age deposits from western Canada and Greenland, and achieved a wide distribution early in its evolutionary history. Exchange of Glyptostrobus between Asia and North America occurred across the Spitsbergen and Beringian corridors, which were functional about 110 and 100 million years ago, respectively The Late Cretaceous fossil record of Glyptostrobus shows that the genus had spread into Russia, China and the shores of the Turgai Strait. By the early Tertiary, Glyptostrobus was a prominent constituent of the polar broad-leaved deciduous forests. Paleocene age deposits across western Canada and the United States indicate the genus was present in great abundance in the lowland warm temperate and subtropical forests east of the Rocky Mountains. The broad distribution in North America and Russia during the Paleocene and Eocene indicates that Glyptostrobus grew and reproduced under a diverse range of climatic and environmental conditions, including the cold and unique lighting conditions of the polar latitudes. The presence of Glyptostrobus in Europe indicates the North Atlantic land bridges that extended between North America and Eurasia (Fennoscandia) and Europe during the early Tertiary were used. In Europe, extensive Glyptostrobus dominated swan1ps occupied the Central European Depression during the late Tertiary. Increasing global aridity and cooling, as well as landscape stabilization together with increasing competition for resources and habitat by representatives of the Pinaceae, seem to have forced the genus out of North America, Europe and most of Asia during the Miocene and Pliocene. In Japan, Glyptostrobus persisted until the early Pleistocene. After the early Pleistocene extinction in Japan, Glyptostrobus reappeared in southeastern China. Details of the taxonomic and biogeographic history of Glyptostrobus are examined.
A decorated pair of trousers excavated from a well-preserved tomb in the Tarim Basin proved to have a highly informative life history, teased out by the authors – with archaeological, historical and art historical dexterity. Probably created under Greek influence in a Bactrian palace, the textile started life in the third/second century BC as an ornamental wall hanging, showing a centaur blowing a war-trumpet and a nearly life-size warrior of the steppe with his spear. The palace was raided by nomads, one of whom worked a piece of the tapestry into a pair of trousers. They brought no great luck to the wearer who ended his days in a massacre by the Xiongnu, probably in the first century BC. The biography of this garment gives a vivid glimpse of the dynamic life of Central Asia at the end of the first millennium.
The species of Rhyacobates Esaki, 1923 are reviewed. Three new species, R. bui sp. nov. from Guangxi, China and Lạng Sơn, Vietnam, R. elongatus sp. nov. from Hà Tĩnh, Vietnam and R. turgidus sp. nov. from Sichuan and Chongqing, China are described. Supplemental descriptions, diagnoses and new distribution records are provided for the fourteen previously known species, i.e., R. abdominalis Andersen & Chen, 1995, R. anderseni Tran & Yang, 2006, R. angustus Tran & Nguyen, 2016, R. chinensis Hungerford & Matsuda, 1959, R. constrictus Tran & Nguyen, 2016, R. edentatus Andersen & Chen, 1995, R. gongvo Tran & Yang, 2006, R. lundbladi (Hungerford, 1957), R. malaisei Andersen & Chen, 1995, R. recurvus Andersen & Chen, 1995, R. scorpio Andersen & Chen, 1995, R. svenhedini (Lundblad, 1934), R. takahashii Esaki, 1923, and R. zetteli Tran & Nguyen, 2016. Photographs and line drawings of the habitus, diagnostic characteristics of both sexes, the habitat and in-situ photographs are presented. A revised key to the species of Rhyacobates is also provided.