116,488 research outputs found
Kirchscene [und] Gartenscene aus Göthe's Faust / Gem. v. Bartsch. Lith. v. Hartwich
No full textKIRCHSCENE [UND] GARTENSCENE AUS GÖTHE'S FAUST / GEM. V. BARTSCH. LITH. V. HARTWICH
Kirchscene [und] Gartenscene aus Göthe's Faust / Gem. v. Bartsch. Lith. v. Hartwich (1)
Illustration 1: Kirchscene aus Göthe's Faust. (1)
Illustration 2: Gartenscene aus Göthe's Faust (3
Der Gläubigen Durst und Lust nach Christo, aus der Offenbahrung Johannis am XXI. cap. v. 6.7. an der Durchlauchtigsten Fürstinnen und Frauen, Frauen Eliesabeht Julianen, Vermähleten Hertzoginnen zu Braunschweig und Lüneburg, [et]c. Da Dieselbe Jm LXX. Jahr Jhres Alters Jhren höchst-rühmlichst geführten Wandel den 4ten Febr. Nachmittags um zwey Uhr anno 1704. seelig beschlossen, Und darauff den 4ten April. selbigen Jahrs zu Wolffenbüttel ... beygesetzet worden, Jn einer Leich-Predigt gehalten, fürgestellet, ... unterthänigst offeriret von M. Rudolph Henrich Rehtmeyer, Past. St. Mich. & Sub-Seniore
No full textAutopsie nach Exemplar der ULB Sachsen-AnhaltVorlageform des Erscheinungsvermerks: Wolffenbüttel, Drukts Christian Bartsch, privilegirter Hof- und Cantzley-Buchdr
A hydrothermal vent mite (Halacaridae, Acari) with a new Corynophrya species (Suctoria, Ciliophora), description of the suctorian and its distribution on the halacarid mite
No full textCopidognathus nautilei Bartsch, 1997, from a hydrothermal vent field of the Mid-Atlantic Ridge at about 13 degrees N, 45 degrees W and 4090 m depth, was infested with the suctorian Corynophrya abyssalis n. sp., with up to 58 epizoans per mite. The new suctorian has a sacciform body with seven longitudinal ribs, a compact macronucleus and up to 40 non-retractile tentacles. The budding is exogenous. The systematic position of the new species and the genus Corynophrya is discussed, as well as infestation rates and sites of suctorians on their halacarid hosts
De Praescriptione Mvtvi, Chirographarii / Dissertationem Academicam VI. Constitvtionis D. Friderici Editam Defendent Io. Guilielm. Gadendam I. V. Et Ph. D. P. P. O. Et Otto. Flor. Kiliensis Ivr. Cand. Ad D. XXV. Nov. CIƆIƆCCLXIX.
No full textKiel, Univ., Jur. Diss., 1769Autopsie nach Ex. der ULB Sachsen-AnhaltVorlageform des Erscheinungsvermerks: Kiliae Litteris Vidvae B. Gottfr. Bartschii Academ, Typogr. - Erscheinungsjahr nach der Datierung im Titel bestimm
V. Germanistische Studien (Supplement zur Germania), herausgegeben von Karl Bartsch. II
No full textP. G. V. Germanistische Studien (Supplement zur Germania), herausgegeben von Karl Bartsch. II. In: Romania, tome 4 n°13, 1875. pp. 148-150
Lolibaia polythyris Bartsch & Sáfián 2019, sp. nov.
No full text<i>Lolibaia polythyris</i> sp. nov. <p>Figs 5–6, 9</p> <p> <b>Holotype ♀:</b> South Africa, KwaZulu-Natal, near Drummond 45 km west of Durban, 1 June 1954, L. Vári leg. (TMSA).</p> <p> <b>Paratype: 1♀,</b> South Africa, Eastern Cape, East London, Beacon Bay, 21.October 1979, N.J. Duke (Bartsch gen. slide No. 2018–25) (TMSA).</p> <p> <b>Description.</b> Alar expanse 38 mm, forewing 17 mm, antenna 14 mm and body length 20 mm.</p> <p>Head: labial palpus dark brown; frons anthracite grey with pearly gloss, some whitish scales laterally; vertex and pericephalic scales dark brown; antenna dark brown, dorso-distal half black, except for a rather short white stripe subdistally.</p> <p>Thorax and legs: black with steel-blue gloss; patagia dark reddish-brown; tarsus of hind leg distally and all pairs of spurs ventrally white. Wings black, with distinct pattern of opaque and transparent areas; forewing with anterior and longitudinal transparent area short, approximately one third of total wing length, external transparent area ovate rounded, somewhat pointed towards tornus, consisting of 4–5 sub-cells, discal spot and opaque distal half of discal cell fused together form an extremely broad medial spot, apical area present, somewhat translucent, as broad as external transparent area; hindwing with discal spot and distal margin broad, the latter with basad pointing projection between veins CuA2 and CuP.</p> <p>Abdomen: black, sternites 1 and 2 laterally white.</p> <p>Female genitalia: Apophysis posterior about one quarter longer than apophysis anterior, the latter twice as long as segment eight; ductus bursae somewhat enlarged, with numerous knobbly, longitudinal folds; corpus bursae round.</p> <p> <b>Variation.</b> The two specimens vary minimally in size, with alar expanses 37 mm and 38 mm respectively. The paratype has further longitudinal and anterior transparent areas of forewing somewhat longer; external transparent area smaller, not pointing; discal spots of both wings narrower; and basal pointing projection of distal margin of hindwing short and blunt.</p> <p> <b>Diagnosis.</b> <i>Lolibaia polythyris</i> appears very distinctive, but a confusion with other <i>Lolibaia</i> species cannot be ruled out keeping in mind the fact that females of the congeneric species remain unknown. The main character easily diagnosing this species from its congeners is the entirely black labial palpus, which is red ventrally in all congeners.</p> <p> <b>Etymology.</b> The name of this species is derived from the ancient Greek <i>polys</i> = many and <i>thyris</i> = window.</p>Published as part of <i>Bartsch, Daniel & Sáfián, Szabolcs, 2019, Further information on Lolibaia Gorbunov & Gurko, 2017 (Lepidoptera: Sesiidae: Synanthedonini) with description of three new species from tropical Africa, pp. 339-348 in Zootaxa 4559 (2)</i> on pages 345-346, DOI: 10.11646/zootaxa.4559.2.7, <a href="http://zenodo.org/record/2627022">http://zenodo.org/record/2627022</a>
Pyropteron nigrobarbata Bartsch & Pühringer & Milla & Lingenhöle & Kallies 2021, stat. nov.
No full textPyropteron nigrobarbata (Rebel, 1916) stat. nov. (Figs 8–10, 75–77, 82, 83, 90) Sesia minianiformis subspec. nigrobarbata Rebel, 1916: Annalen des k.k. Naturhistorischen Hofmuseums, 30: 144. Syntypes: 2♀, Greece, Crete, Asitaes [Lefka Ori] and Kristallenia [Lassithi plain] (lost? Not in NHMW). Diagnosis. This species is very similar in coloration and pattern to P. minianiformis, but differs from all its subspecies by the smaller size, with alar expanses from 12 to 17 mm (15–24 mm in P. minianiformis), and the almost completely black thorax, which has only some yellow scales on the lateral part of the patagia and on the scapular spot of the forewing base (inner margin of tegula and dorso-lateral scale tufts of metathorax mainly yellow in all subspecies of P. minianiformis). Males differ further by the lack of black scales in the orange parts of the forewing (especially anal margin and cubitus vein suffused with black scales in P. minianiformis). Females differ by the presence of black scales ventrally on labial palpus (purely orange in P. minianiformis). Occasionally, almost completely black specimens of P. nigrobarbata occur. The male genitalia of P. nigrobarbata are very similar to that of P. minianiformis. There are, however, some distinct differences in the female genitalia, which are much more compact in P. nigrobarbata, the papillae anales and segment eight as well as ductus bursae and corpus bursae are shorter and broader, and the ductus bursae is gradually enlarged into a rounded corpus. In P. minianiformis, the ductus bursae is consistently narrow, the corpus elongated and somewhat pear-shaped. Barcodes. Based on barcode analyses, P. nigrobarbata represent the oldest clade in the minianiformis group of taxa and is the sister species of P. minianiformis. Biology and habitat. The larvae were found in the roots of Rumex pulcher Linnaeus, sometimes numerous larvae together (pers. observation Mai). Furthermore, in the Asterousia Mts two females have been observed depositing eggs on Rumex acetosella Linnaeus, indicating that it constitutes another hostplant. Indeed, Rumex acetosella is often the only available hostplant in heavily grazed places in Crete where adults were observed. It grows sheltered between the thorny cushions of Sarcopoterium spinosum (Linnaeus) Spach (Rosaceae) where it is protected from goats. Several attempts to find larvae in other species of Rumex were unsuccessful. Males are attracted to various artificial pheromons from the late morning to early afternoon. Distribution. Endemic to Crete. Specimens examined. 1♂, Greece, Crete, Frango Castello, 29. V.1998, leg. RB (Bartsch gen. prep. 2019-09) (Fig. 82); 5♂, Greece, Crete, Ida, Mt Samari, 1400m, 27. V.2000, leg. AL; 7♂, Greece, Crete, Ida above Kourites, 1200–1400m, 17. and 23. V.2011, leg. DB; 1♂, Greece, Crete, Agios Joannis, 1. VI.1998, leg. RB (Bartsch gen. prep. 2019-12) (Fig. 83); 2♂ (Figs 75–76), 2♀, Greece, S Crete, Asterousia Mts, pass between Loukia and Kapetaniana, 21. V.2011, leg. DB (Bartsch gen. preps. 2019-13, 2019-14) (Fig. 90); 1♂, ibid., 31. V.2000, leg. AL; 1♂, Greece, Crete, Rethimnon, 20km N Agia Galini, Kouroutes, 600m, 29. V.2000, leg. AL (CDB). 1♂, Greece, S Crete, Asterousia Mts pass between Loukia and Kapetaniana, 24. V.2010, 1♀, ibid., (Fig. 77), leg. AL (CAL); 8♂ Greece, Crete, entry to Samaria Gorge, near Omalos, 1300m, 22.–23. VI.2018, leg. A. Kallies (CAK); 2♂, Greece, Crete, Chania, Omalos-Hochebene, Lefka Ori S, 1150 m, 2.VII.2004, leg. FP (CCDB-02113 F02); 3♂, Greece, Crete, Rethymnon, Kouroutes, 9. VI.2000, leg. FP (CCDB-04642 D07); 2♂, Greece, Crete, Rethymnon, Nithavris (Ida Mts), 9. VI.2000, leg. FP (CCDB-04642 D06); 2♂, Greece, Crete, Iraklion, Asterousia Mts, Loukia, 2. VI.1998, leg. RB (BOX-2219 F03, gen. prep. FP 02/16, 02/17) (CFP).Published as part of Bartsch, Daniel, Pühringer, Franz, Milla, Liz, Lingenhöle, Arthur & Kallies, Axel, 2021, A molecular phylogeny and revision of the genus Pyropteron Newman, 1832 (Lepidoptera, Sesiidae) reveals unexpected diversity and frequent hostplant switch as a driver of speciation, pp. 1-75 in Zootaxa 4972 (1) on pages 27-31, DOI: 10.11646/zootaxa.4972.1.1, http://zenodo.org/record/477179
Pyropteron jordanicum Bartsch, Puhringer, Lingenhole & Kallies 2021, sp. nov.
No full textPyropteron jordanicum Bartsch, Pühringer, Lingenhöle & Kallies sp. nov. (Figs 23, 152–155, 166–168, 226) This species was recorded as P. pipiziformis from several localities in Israel by Freina & Lingenhöle (2000). The same authors also gave a brief description and illustrate the variability of the male genitalia. Almost the entire type series was captured by Lingenhöle, who donated specimens to other collections. Description. Male. Alar expanse 11.0–18.0 mm (holotype 17.0 mm). Head almost entirely brownish-black; inner side of labial palpus white ventrally; frons additional with purple shine; vertex glossy black; pericephalic scales orange, laterally somewhat paler; antenna dorsally with white, subapical patch or even with some white scales. Thorax black with steel-blue gloss; patagia and mesothorax ventro-laterally with large orange patch. Legs black with steel-blue gloss; tarsus white, slightly mixed with dark grey distally, first tarsomere on proximal half dark grey; spurs white; fore leg with lateral half of coxa white and tibia ventrally with tuft of pale brownish-yellow scales; tibia of mid and hind leg with large white patch laterally. Wings black with steel-blue gloss; forewing transparent areas well developed; the PTA reaching discal spot; ETA consisting of 5–6 cells; discal spot narrow; apical area absent; hindwing discal spot short and narrow. Abdomen black with steel-blue gloss, laterally with longitudinal, orange stripe, widened distally on sternites 4–7; tergite 4 orange; anal tuft black. Male genitalia. Gnathos flaps well-developed, ovoid, the middle one distally shorter; crista sacculi medially flattened, distally very high, setae subdistally mostly but not always with a more or less large gap. Female. Alar expanse 13.0–15.0 mm. Similar to male, but antenna without white scales; tarsus of all legs black; spurs ventrally brownish-black; transparent areas smaller, the PTA not reaching the discal spot; ETA consisting of 5 cells, first and last one very short; apical area present. Diagnosis. The male of P. jordanicum differs from that of P. pipiziformis as follows: ETA very large (smaller in P. pipiziformis); apical area reduced (well-developed in P. pipiziformis); forewing discal spot somewhat smaller, caudally narrowed; white elements of the legs more prominent; anal tuft black (basally and laterally suffused with orange in P. pipiziformis). The male genitalia are very similar to that of P. pipiziformis, but have the setaceous area well separated from the distal portion of the crista sacculi (connected by a narrow stripe of setae in P. pipiziformis). The difference in the DNA barcode of the two species is large, with more than 5%. Both, P. pipiziformis and P. jordanicum sp. nov. are similar to P. atypica. With more than 20 mm wingspan the latter species is, however, distinctly larger, has its head and thorax entirely black, lacks white markings of the legs, has the proximal half of tibia of mid and hind leg dorso-laterally pale orange and a ventrally closed orange ring on abdominal segment four. Variation. There is little variation in the external appearance of this species. Specimens from Jordan are somewhat larger than those from Israel and have sometimes the stalk of veins R4 and R5 extremely long. Occasionally there are specimens with the space between veins R4 and R5 filled with scales, not partially hyaline as usually. One specimen from Beit Zayit, Israel, has the coxa of the fore leg nearly completely white. A relatively large variability is seen in the crista sacculi of the male valve. The field of setae can be continuous or have a clear gap (Freina & Lingenhöle 2000). Barcodes. This species is sister to the previous with an average distance of 5.6%, while the average intraspecific variation is just above 1%. Biology and habitat. The hostplant is unknown. Freina & Lingenhöle (2000) report that numerous specimens were collected in ruderal places in Israel with the help of various artificial pheromones. Males attracted to pheromones fly very low, close to the ground (pers. observation Lingenhöle). Distribution. So far known from Israel and Jordan (Freina & Lingenhöle 2000). Etymology. This species is named after the river Jordan, whose banks are in the centre of its distribution area. Specimens examined. Holotype ♂ (Figs 153–154) with labels: “ Israel / Süd Golan / Umg. Eli Al 350 m / 30.4.– 1.5.1999 / leg. Lingenhöle ”; “ Holotypus / Pyropteron / jordanicum / ♂ / D. Bartsch, des. 2020” (SMNS). Paratypes: 105♂, 1♀, same data as holotype (Fig. 155) (1♂ AL gen. prep. 101) (Fig. 167); 37♂, Israel, 15 km W Jerusalem, Beit Zayit, 700m, 8. V.1999 (3♂ AL gen. prep. 108, 109, 110); 43♂, Israel, North Golan, vic. Banyas, 500m, 3.–4. V.1999 (3♂ AL gen. prep. 102, 111, 112) (102, Fig. 168), (1♂ Bartsch gen. prep. 2019-27) (Fig. 166) (BOLD DB-Lep-00013); 4♂, N-Israel, Meron Mts, vic. Zefat, 5km S Meron, 5. V.1999; 4♂, Israel, Galiläa, Gilboa Mts, Ha-Gilboa Res., 350m, 28.–29.IV.1999; 2♂, N-Israel, Mount Kamal, vic. Isfiya, 400–500m, 5. V.1999, all leg. AL (SMNS, CAK, CAL, CDB, CTG, CTS); 1♀ (Bartsch gen. prep. 2020-06) (Fig. 226), Israel, Mt. Carmel-Nahal Nesher, 14. VI.2000, leg. Török (slide DB 2020-06, SMNS); 7♂, Jordan, Ajloun gouvernorate, Ajloun, 32°19’49,4’’N, 35°43’46,2’’E, 28. V.2009, leg. Stalling; 1♂, same locality, 32°19’N, 35°44’E, 29. V.2009, leg. Stalling; 3♂, Jordan, Irbid Gouv., Jadita, Wadi Yabis, 32°24’00’’N, 35°40’22’’E, 260m, 28. V.2009, 11:00 h, leg. Stalling (CTS); 1♂, Jordan, Prov. Ajloun, Ajloun, 08. V.2008, leg. W. Garrevoet (CTG); 4♂, Israel, Golan, vic. Eli Al, 350 m, 30.IV.-1. V.1999, leg. AL; 3♂, Israel, Beit Zayit w. Jerusalem, 700 m, 8. V.1999, leg. AL (BOX-2219 A02); 1♂, Israel, Nord-Golan, Banyas — Umg., 500 m, 3.–4. V.1999, leg. AL (CFP).Published as part of Bartsch, Daniel, Pühringer, Franz, Milla, Liz, Lingenhöle, Arthur & Kallies, Axel, 2021, A molecular phylogeny and revision of the genus Pyropteron Newman, 1832 (Lepidoptera, Sesiidae) reveals unexpected diversity and frequent hostplant switch as a driver of speciation, pp. 1-75 in Zootaxa 4972 (1) on pages 50-51, DOI: 10.11646/zootaxa.4972.1.1, http://zenodo.org/record/477179
Conopsia puehringeri Sáfián & Bartsch 2018, sp. nov.
No full textConopsia 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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