340 research outputs found
Bartsch (Kurt), Baur (Uwe), Goltschnigg (Dietmar), hrsg. Horvath-Diskussion
Tindemans C. Bartsch (Kurt), Baur (Uwe), Goltschnigg (Dietmar), hrsg. Horvath-Diskussion. In: Revue belge de philologie et d'histoire, tome 61, fasc. 3, 1983. Langues et littératures modernes — Moderne taal- en letterkunde. p. 647
Bartsch (Kurt), Baur (Uwe), Goltschnigg (Dietmar), hrsg. Horvath-Diskussion
Tindemans C. Bartsch (Kurt), Baur (Uwe), Goltschnigg (Dietmar), hrsg. Horvath-Diskussion. In: Revue belge de philologie et d'histoire, tome 61, fasc. 3, 1983. Langues et littératures modernes — Moderne taal- en letterkunde. p. 647
Wolfgang Bauer
Kurt Bartschs Beitrag über Wolfgang Bauer ist eine kompakte Einführung in dessen Gesamtwerk. Bartsch, der Bauers dramatisches Werk gegen die Zuordnung zum neuen kritischen Volksstück eines Franz Xaver Kroetz oder Peter Turrini in Schutz nimmt, weist mittels close reading nach, dass Bauer von seinem ersten, vom absurden Theater Ionescos beeinflussten Einakter, Der Schweinetransport, bis zu Magnetküssen (1975), Skizzenbuch (1994/95) und Café Tamagotchi (1998), mittels seines Metatheaters permanent das Prinzip der Wirklichkeit in Frage stellt. Dabei ist dem Werk Bauers, welches nicht nur die Schranken zwischen E- und U-Kultur aufhebt, sondern stets die Gattung selbst reflektiert, die permanente Auseinandersetzung mit avantgardistischen Kunstrichtungen eingeschrieben
"Heimat ist, wo irgendeiner wohnt". Reinhard P. Gruber, der "Heimatentheoretiker"
Angesichts von Flüchtlingsströmen und dem Wiederaufleben national getönter Heimatdebatten stellt sich heutzutage erneut die Frage nach der Bedeutung von Heimat und Zuhausesein. In seinem Beitrag „‚Heimat ist, wo irgendeiner wohnt.’ Reinhard P. Gruber, der ‚Heimatentheoretiker’“ untersucht der Grazer Literaturwissenschaftler Kurt Bartsch ausgehend von dessen Punzierung als „satirischer Heimatdichter“ Grubers Umgang mit dem ideologisch überfrachteten Begriff. Beginnend mit unterschiedlichen Definitionen (als Besitz, Territorium, Idylle, Ort, wo „noch niemand war“) zeigt Bartsch anhand der drei Texte Heimat ist, wo das Herz weh tut. 35 Fragmente eines konkreten Beitrags zu einer antiutopischen Heimatentheorie, Heimatlos. Eine steirische Wirtshausoper in einem Rausch und Aus dem Leben Hödlmosers. Ein steirischer Roman mit Regie Grubers augenzwinkerndes Unterlaufen jedweder Heimatideologie durch Verfahrensweisen der Wissenschafts- und Sprachsatire wie auch der Textklassenparodie (von tautologischen Argumentationen über übertriebene Affirmation bis zur ironisierenden Konfrontation unterschiedlicher Textmodelle) auf und verortet dessen Schreiben – in Abgrenzung vom sog. Antiheimatroman wie auch dem kritischen Volksstück – im Bereich des Karnevalesken, das auf die subversiv-befreiende Wirkung des Lachens setze
Acarothrix palustris Bartsch 1990
<i>Acarothrix palustris</i> Bartsch, 1990 <p>(Figs. 17-20)</p> <p> <i>Acarothrix palustris</i> Bartsch, 1990: 205-207, figs. 1-14.</p> <p> <b> <i>Material examined.</i> –</b> One female, ZRC.ARA.483, Singapore, northern coast, end of Lim Chu Kang Road, <i>Cladophora</i> mat on muddy and sandy sediment, coll. I. Bartsch, 7 Oct.2004; one larva, ZRC.ARA.484, collecting data as above; one female, SMF, collecting data as above; one female, ZMH, collecting data as above; one male, ZMH, collecting data as above; one protonymph, ZMH, collecting data as above. One larva, author’s collection, Singapore, southern coast, river Pandan, sediment, green algae and epibiota on <i>Avicennia</i> pneumatophores in a rockpool, coll. I. Bartsch, 27 Sep.2004.</p> <p> <b> <i>Diagnosis.</i> –</b> Length of idiosoma 280-320 µm. PD with pair of longitudinal porose costae with narrow cerotegumental ridges, remainder of plate reticulate. OC with two corneae. PD with two pairs of gland pores. Pair of ds- 2 in margin of OC. Pair of ds-4 and ds- 5 in lateral margin of PD, almost equidistant relative to anterior pair of gland pores. Female and male GA almost ovate. Male GA with 11-12 pairs of pgs, interval between anterior margin of GA and that of GO equalling length of GO. Tibiae I and II with six setae each. Tibiae I to III each with one bipectinate and one smooth, slender ventral seta; on tibiae IV both ventral setae smooth and slender. Paired claws almost smooth.</p> <p> <b> <i>Colour.</i> –</b> Gut content pale or slightly brown; the male examined darker than females. Dorsum with three small black eye spots.</p> <p> <b> <i>Complementary description.</i> – Adults:</b> Length of female 294- 320 µm, of male 280 µm. Shape of dorsal plates as illustrated (Fig. 17). Costae of PD approximately 20 µm wide, with narrow cerotegumental borders. Pair of epimeral pores at end of apodemes between epimera I and II (Fig. 18); porus covered with numerous setiform tines. Male with 11-12 pairs of pgs; its GO large, distance to anterior margin of GA equalling length of GO (Fig. 19). Basi- and telofemora I and II with numerous filaments, trochanters, basi- and telofemora III and IV with filaments fused to cerotegumental lamellae. Leg chaetotaxy: leg I, 1, 2, 5, 4, 6, 6; leg II, 1, 3, 5, 4, 6, 4; leg III, 1, 2, 2-3, 3, 5, 4; leg IV, 1, 2, 2-3, 3, 5, 3. Telofemora III and IV in general with 2/1 dorsal/ventral setae, rarely ventral seta absent. Tibiae I, II and III each with short, wide bipectinate seta, on tibia IV this seta slender and smooth. Claws almost smooth though vestiges of accessory process present. Median claw of all tarsi bidentate, that claw of tarsus III and IV with long upper and lower tooth and therefore median claws somewhat larger than on tarsi I and II.</p> <p> <b>Protonymph:</b> Length of idiosoma 217 µm. Dorsal and ventral plates smaller than in adults. Leg chaetotaxy: leg I, 1, 2, 3, 4, 5, 6; leg II, 1, 2, 3, 4, 5, 4; leg III, 1, 2, 2, 3, 5, 3; leg IV, 0, 1+2 (basi- plus telofemur), 3, 5, 3. Tibiae I, II and III each with one of the two ventral setae being short, wide and pectinate, the other seta slender and smooth. Tibia IV with two smooth ventral setae. Both tarsi III in the protonymph examined with three instead of four dorsal setae.</p> <p> <b>Larva:</b> Length of idiosoma 177 µm. Shape of dorsal and ventral plates as illustrated in Bartsch (1990: figs. 8 and 9). PD with pair of cerotegumental ridges. Pair of epimeral pores at about the level of end of apodemes. Leg chaetotaxy: leg I, 1, 1+3 (basi- plus telofemur), 4, 5, 6; leg II, 1, 1+3, 4, 5, 4; leg III, 1, 1+2, 3, 5, 4. Pectinate seta of tibia I and II wide, less than height of each segment. Tibia III with two almost smooth ventral setae. Distance between two basal setae of tarsus III more than height of that segment (Fig. 20).</p> <p> <b> <i>Remarks.</i> –</b> The PD and GA of the Singapore specimens illustrated are slightly more slender than in the holotype and paratype from Hong Kong. The width of the plates proved to vary slightly in the material from Singapore.</p> <p> The adults of the two <i>Acarothrix</i> species (<i>A. ampliumeris</i> and <i>A. palustris</i>) present in Singapore mangroves can be distinguished on the basis of the length of OC, presence or absence of corneae, shape of AE, length of PE, and shape of ventral setae on tibiae II and IV. Juveniles which have small dorsal and ventral plates can be distinguished on the basis of presence or absence of corneae, position of epimeral pores relative to length of apodemes, and size of the median claws on the posterior tarsi. In addition, larvae can be distinguished on the basis of presence or absence of cerotegumental ridges on the PD and position of the basal seta on tarsus III.</p> <p> <i> <i>Distribution. –</i> Acarothrix palustris</i> inhabits mangroves in Hong Kong and Singapore (Bartsch, 1990, and present record).</p>Published as part of <i>Bartsch, Ilse, 2006, Copidognathines (Acari: Halacaridae) In Mangroves Of Singapore. I. Description Of Three Species, pp. 83-92 in Raffles Bulletin of Zoology 54 (1)</i> on page 87, DOI: <a href="http://zenodo.org/record/4507985">10.5281/zenodo.4507985</a>
Agauopsis arabia Bartsch and Chatterjee 2001
<i>Agauopsis arabia</i> Bartsch and Chatterjee, 2001 Figure 1 A-E <p> <i>Agauopsis arabia</i> Bartsch and Chatterjee 2001: 322- 326, fig. 1-12.</p> <p> Additional material examined — Two females, Bay of Bengal, Andaman Islands (by T. Chatterjee forwarded to the author for identification; cf. Chatterjee <i>et al.</i>, 2004).</p> <p> Short description — Length of female 450 – 490 µm, of male 416 µm (according to Chatterjee <i>et al.</i>, 2004, female 450 – 500 µm, male 410 – 450 µm). Dorsal plates with costae. Surface of costae not reticulated but canaliculi arranged in groups. Integument between costae with epicuticular droplets forming a reticulum; canaliculi within reticulum (polygons) more delicate than within costae. AD slightly more than 1.2 times longer than wide. Transverse costa on AD at about 0.5 and more narrow than longitudinal costae, middle part slightly curved posteriad (Figure 1A). Pair of ds-1 level with gland pores. OC 1.4 times longer than wide; glp on OC removed from posterior cornea, situated about halfway between that cornea and pc (Figure 1B) or at 0.4 along lateral margin of OC. PD of female and male almost equal-shaped, 1.2-1.3 times longer than wide. Medial costae on PD rather narrow, width in middle part of plate equalling three groups with canaliculi, else costae two groups wide. Pair of ds-4 level with or immediately posterior to edge of OC; pair of ds- 5 in anterior half of PD, outside costae, pair of ds-6 on PD.</p> <p>Ventral plates faintly reticulated, with rather evenly spread canaliculi within each polygon, mostly with (6-)11-17(-18) canaliculi per polygon. Anterior margin of female GA truncate, that of male slightly convex. Male with 36-39 pgs around GO and pair of outlying setae. That pair of setae about halfway between ring of pgs and lateral margin of GA. Interval between anterior margin of each GA and GO equalling about length of GO. Spermatopositor large, 0.7 of length of GA and extending to anterior margin of that plate.</p> <p>Length of gnathosoma 2.1-2.2 times its width. Rostrum somewhat longer (1.1-1.2 times) than gnathosomal base. P-2 2.7-2.9 times longer than high (Figure 1D). P-4 twice as long as P-3, its two basal setae almost equal in length. Tectum with scaliform lamella (Figure 1C).</p> <p>Tibia II ventrally with one bipectinate and two dentate, spiniform setae. Tibiae III and IV with two dentate, spiniform setae. Telofemora III and IV 2.0-2.2 times longer than high. Ventral seta on telofemora III and IV in apical half. Tarsi III and IV with short lateral fossa membranes. Claws II to IV each with minute accessory process and pectines with delicate tines (Figure 1E).</p> <p> Remarks — The rostrum of <i>Agauopsis arabia</i> is slightly longer than the gnathosomal base whereas in most of the species mentioned from the tropical Indo-West Pacific the rostrum is shorter than the base, exceptions are <i>A. longirostris</i> Bartsch, 2015 and <i>A. moorea</i> Bartsch, 1992. The rostrum of <i>A. longirostris</i> is distinctly longer (1.7-1.8 times) than the basis, that of <i>A. moorea</i> 1.0-1.1 times longer. Differences between <i>A. arabia</i> and <i>A. moorea</i> are in the position of the gland pore on the OC, in the anterior (<i>A. arabia</i>) and posterior half (<i>A. moorea</i>); furthermore, males of <i>A. moorea</i> have a small spermatopositor which does not extend to the anterior margin of the GA.</p> <p> Distribution and Biology — Arabian Sea (Goa, Kerala), Bay of Bengal (Andrah Pradesh, Andaman Islands) (Bartsch and Chatterjee 2001; Chatterjee <i>et al.</i> 2004; Chatterjee and Guru 2011). Most records are from tidal algae.</p>Published as part of <i>Bartsch, I., 2015, The Agauopsis brevipalpus group (Acari: Halacaridae), descriptions of tropical Indo-West Pacific species, a key to all species, their geographical distribution and reflections on dispersal routes, pp. 147-169 in Acarologia 55 (2)</i> on pages 149-150, DOI: 10.1051/acarologia/20152158, <a href="http://zenodo.org/record/5403910">http://zenodo.org/record/5403910</a>
Der Löwe mit der besonders schönen langen Mähne
This is a long and enjoyable development of a Kalila and Dimna story usually told about a hare and a lion. Here a mouse takes the place of the hare. At least in some versions of Kalila and Dimna, the story has to do with regulated sacrifice. Here the inciting incident is that the mouse not only does not proclaim You are the king of the animals but even says out loud You are not the strongest. The mouse then, when he has the lion's attention, cleverly says that he is sad because the lion will not much longer be king. He gets the lion to be inquisitive about this stronger competitor. The mouse even asks the king if he might be afraid of this competitor, and all the animals recognize that the lion lies in his answer. The mouse then offers to help the lion by showing him the way to this competitor. The lion rejects that offer, since it would take days to get there; of course he then offers to take the mouse on his back. The lion has overnight to think about it -- and of course to let his fear increase. In this version, the mouse throws a little stone into the well to make the lion there move and seem to swim. The best illustration of a strongly illustrated book comes next as the lion is absolutely perpendicular to the horizon in his dive into the well. At last the animals have quiet, but do not know that it has come from a mouse.This is a hardbound book (hard cover)Language note: German4. AuflageKurt Davi
Camaegeria viettei Bartsch & Berg, 2012, n. sp.
<i>Camaegeria viettei</i> n. sp. <p>Figs. 28–29, 37</p> <p>Holotype 3 (Figs. 28–29, 37): Madagascar Est: Moramanga, vic. Andasibe, garden of the hotel Feon n’y Ala S/W of Foret de Analmazaotra NP, 800 m, 18°56’53.3’’S 48°25’08.2’’E, 26.XI.2006, J. Berg & D. Bartsch leg. (SMNS). The holotype was attracted by artificial pheromones during late morning hours.</p> <p> <b>Etymology.</b> This beautiful species is dedicated to Pierre Viette, the author of the first Sesiidae fauna of Madagascar, with deep respect for and in honour of his lifework.</p> <p> <b>Description.</b> Alar expanse 19.5 mm, forewing 8.5 mm, antenna 6.5 mm, body 10 mm. Labial palp bright orange-yellow, dorsally black, second palpomere dorso-apically yellow; frons dark grey with blue-metallic gloss, white adjacent to the eye; vertex glossy black, between antenna and ocellus with narrow orange-yellow spot and with tufted orange-yellow, hair-like scales; antenna dorsally black with blue gloss, ventrally brown; pericephalic scales orange-yellow, dorsally mixed with black. Thorax black with blue gloss; mesothorax dorsally with small yellow medial spot and intensive whitish-blue shining anterior margin, laterally with orange-red stripe; tegula orange-yellow, antero-laterally white, posteriorly with some orange-red scales. Abdomen short and strong; tergites anteriorly black, posteriorly somewhat lighter brown-black with blue-violet gloss; sternites 1 and 2 white; anal tuft short, dark brown-black, laterally with some pale brown scales and outside of valva whitish. Legs brown-black with intense violet gloss; foreleg with coxa laterally narrow yellow; femur ventrally whitish; tibia ventrally yellow, laterally with tufts of long, brown-black, iridescent violet scales, on mesal side dorsally orange; tarsus black. Midleg with first tarsomere very long, as long as tibia, the latter with tufts of long and rough hair-like scales. Hindtibia very long, twice as long as femur, proximal half ventrally white, distal half with long and rough scale tufts; tarsomere 1 dirty white with some brown-black scales, other tarsomeres black and mesally whitish-yellow; spurs brown-black, laterally white. Wings hyaline; forewing with common stalk of R4/R5 relative short; longitudinal transparent area extending to discal spot; external transparent area very large, seven-partite; apical area absent; discal spot very narrow, dark brownish-grey, same as veins and margins; anal margin medially, radius stem distally and radius and cubitus branches basally yellow-brown. Hindwing with discal spot very small, reaching M2; discal spot, veins and margins pale yellow, distal part of veins and distal margin dark brownish-grey; fringes brownblack, at anal corner of hindwing yellowish to white. Underside of both wings yellowish, distally black. The male genitalia (Fig. 37) with valva oval with the bald area distinctly longer than 1/3 of its total length; phallus as long as valva with distinct distal tooth; saccus rather narrow, apically rounded. The female is unknown.</p> <p> <b>Diagnosis.</b> <i>Camaegeria viettei</i> is easily recognised by its typical pattern and the beautiful violet gloss on the underside. The male genitalia are very similar to that of <i>C. polytelis</i> and <i>C. xanthomos</i>, but differ by the shorter, broader and apicaly more rounded valva.</p>Published as part of <i>Bartsch, Daniel & Berg, Jutta, 2012, New species and review of the Afrotropical clearwing moth genus Camaegeria Strand, 1914 (Lepidoptera: Sesiidae: Synanthedonini), pp. 28-46 in Zootaxa 3181</i> on pages 40-45, DOI: <a href="http://zenodo.org/record/212257">10.5281/zenodo.212257</a>
Conopsia puehringeri Sáfián & Bartsch 2018, sp. nov.
Conopsia puehringeri sp. nov. (Figs. 1A, B; 2A, B, C) Holotype: ♂ GUINEA, Nimba Mountains, Cité 1, SMFG concession area. Coordinates: 7°42'2.83"N, 8°23'58.60"W, altitude: 730 m asl., pheromone lures, 17–25.V.2017 Leg.: Sáfián, Sz. ANHRT code: ANHRT00029045. Deposited in ANHRT. Paratypes: 8♂♂ GUINEA, Nimba Mountains, Cité 1, SMFG concession area pheromone lures, 17–25.V.2017 ANHRT codes: ANHRT00029046, ANHRT00029047, ANHRT00029048, ANHRT00029049, ANHRT00029051, ANHRT00029052, ANHRT00029053, ANHRT00029054; 1♂ GUINEA, Nimba Mountains, Cité 1, SMFG concession area pheromone lures 17–25.V.2017. Gen. prep.: SAFI00244, ANHRT code: ANHRT00029050; 1♂ GUINEA, Nimba Mountains, Cité 1, SMFG concession area pheromone lures 08. VI.2017. ANHRT code: ANHRT00029058 (deposited in ANHRT); 2♂ GUINEA, Nimba Mountains, Cité 1, SMFG concession area pheromone lures 20–31.V.2017 (deposited in SMNS). Etymology. The species is named to honour Franz Pühringer and his work on Sesiidae. Franz also supported the senior author’s interest on African Sesiidae, and helped him to build an important collection. Description. Alar expanse: 19.5 mm. Head black with strong silvery gloss; labial palpus completely and pericephalic scales laterally orange-red; eye bald, black; antenna black, filiform, slightly pillose. Thorax brick-red dorsally, laterally and ventrally somewhat paler orange-red. Legs orange-red; foreleg with tibia and tarsus dorsally black; midleg dorsally with small black spots at tibia proximally and distally, first tarsomere dorso-distally, other tarsomeres dorsally throughout black; hindleg with tibia and first tarsomere dorsodistally, other tarsomeres completely black. Forewing opaque, shiny black, basally small red. Hindwing basally transparent, distally increasingly opaque, dark grey. Ciliae (fringes) of all wings hair-like, black. Abdomen dorsally brick-red with prominent black longitudinal stripe on tergites 2–7, ventrally orange-red. Anal tuft small, dorso-ventrally flat, black, medially red and ventro-basally with some red scales. Female unknown. Variation insignificant. Male genitalia. Generally weakly sclerotised; uncus long, pointy with strong sclerotized tip, slightly hairy; tegumen broad, angled dorsally; saccus very long, narrow, lanceolate; valvae bi-lobed, upper lobe thumb-like with rounded tip, lower lobe gently pointed; aedeagus (phallus) very long and slender, longer than valva and saccus together. Diagnosis. Conopsia puehringeri sp. nov. could be confused only with the presumably closely related C. bicolor, however, it is generally slightly smaller with characteristic black stripe present on the dorsal side of the abdomen (stripe missing in C. bicolor). Further diagnostic characters are: forewing base small red (more extensive red in C. bicolor, particularly along the costa); no red colour is present on hindwing (semi-transparent area on hindwing edged with red in C. bicolor); antenna completely black (tip red in C. bicolor); male genitalia with bilobed valva (trapezoid in C. bicolor, ending in a single blunt tip). Behaviour, habitat and distribution. All specimens were captured at a mixture of pheromone lures synthesised for 15, predominantly Western Palearctic Sesiidae species. Specimens were attracted between 15.30 and 17.00 h at the beginning of the rainy season in mid-altitude savannah and upland forest mosaic in the Nimba Mountains, Guinea. The species’ distribution or habitat requirements are difficult to conclude from the limited material available, however, C. puehringeri sp. nov. could easily be a restricted range species, specialised in upland habitats in the Guinea Highlands or distributed in the Liberian sub-region of West Africa. Using pheromones lures two months later and at the same locality, Conopsia bicolor was also captured in a series of over 20 specimens. The latter species was also found by the senior author in recent years in Liberia and Ghana, as well as together with Franz Pühringer and Norbert Pöll in Ghana in 2011. Furthermore, the series of C. bicolor specimens presented in Kallies (2000) from Nigeria was also collected with the help of pheromones. Overall, these data suggest a wide, West African distribution of C. bicolor. During these earlier surveys, no specimens of C. puehringeri have been collected.Published as part of Sáfián, Szabolcs & Bartsch, Daniel, 2018, A new species of Conopsia Strand, 1913 (Lepidoptera: Sesiidae: Tinthiinae) from West Africa, pp. 147-150 in Zootaxa 4524 (1) on pages 148-150, DOI: 10.11646/zootaxa.4524.1.12, http://zenodo.org/record/261029
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