107,392 research outputs found
Satan und die Satanisten : ideengeschichtliche Untersuchungen zur Herkunft der komplexen Gestalt "Luzifer/Satan/Teufel", ihrer weiblichen Entsprechungen und ihrer Anhängerschaft / Karl R. H. Frick
No full textSATAN UND DIE SATANISTEN : IDEENGESCHICHTLICHE UNTERSUCHUNGEN ZUR HERKUNFT DER KOMPLEXEN GESTALT "LUZIFER/SATAN/TEUFEL", IHRER WEIBLICHEN ENTSPRECHUNGEN UND IHRER ANHÄNGERSCHAFT / KARL R. H. FRICK
Satan und die Satanisten : ideengeschichtliche Untersuchungen zur Herkunft der komplexen Gestalt "Luzifer/Satan/Teufel", ihrer weiblichen Entsprechungen und ihrer Anhängerschaft / Karl R. H. Frick
Das Reich Satans : Luzifer, Satan, Teufel und die Mond- und Liebesgöttinnen in ihren lichten und dunklen Aspekten ; eine Darstellung ihrer ursprünglichen Wesenheiten in Mythos und Religion (Teil 1) (1)
Die Satanisten : Materialien zur Geschichte der Anhänger des Satanismus und ihrer Gegner (Teil 2) (1)
Satanismus und Freimaurerei : eine Dokumentation bis zur Gegenwart (Teil 3) (1
Geologic atlas of the United States : topography, areal geology, economic geology, structure sections / 110 Latrobe Folio : Pennsylvania
No full textH. M. Wilson ; A. H. Thompson ; J. D. Forster ; Frank Sutton ; H. C. Frick Coke Co.List of Sheets: Topography, Areal Geology, Economic Geology, Geologic StructureIndirektes handschriftliches Exlibris: "1906, 509", das ist United States Geological Survey Washington Exemplar der ETH-BI
Caracladus zamoniensis Frick & Muff, 2009, spec. nov.
No full text<i>Caracladus zamoniensis</i> spec. nov. <p>(Figs 48–58)</p> <p> <i>Caracladus avicula,</i> Lessert 1907: 108, figs 5–6, ♂ misidentified; Lessert 1910: 160, figs 98–99, ♂ misidentified.</p> <p> <b>Type material.</b> <b>HOLOTYPE: Switzerland:</b> <i>Grisons</i>: Sur, Alp Flix, Salategnas, 1960 m [46°31'11.00'' N, 9°38'46.00'' E], 1♂ 24.x.2007, litter sieving, close to the edge of a subalpine forest of Norway spruce (<i>Picea abies</i>), leg. H. Frick, P. Muff, S. Klopfstein, det. H. Frick (NMBE Ar6741). <b>PARATYPES: Switzerland:</b> <i>Grisons</i>: Sur, Alp Flix, Salategnas, 1960 m [46°31'11.00'' N, 9°38'46.00'' E], 3♂ 4♀ 24.x.2007, litter sieving, close to the edge of a subalpine forest of Norway spruce (<i>Picea abies</i>), leg. H. Frick, P. Muff, S. Klopfstein, det. H. Frick (NMBE AR 6742); Sur, Alp Flix, Salategnas, 1960 m [46°31'09.01'' N, 9°38'50.07'' E], 1♀ 17.x.–06.v.2005, pitfall trap, in spruce forest, leg. P. Muff, det. H. Frick (NMBE Ar6736) (Muff <i>et al.</i> 2007); Sur, Alp Flix, Salategnas, 1960 m [46°31'11.00'' N, 9°38'46.00'' E], 1♂ 19.ix.–16.x.2005, pitfall trap, in spruce forest, leg. P. Muff, det. H. Frick (NMBE Ar6735) (Muff <i>et al.</i> 2007); Sur, Alp Flix, Salategnas, 1960m [46°31'11.00'' N, 9°38'46.00'' E], 1♀ 27.v.-24.vi.2005, pitfall trap, in spruce forest, leg. P. Muff, det. H. Frick (MHNG) (Muff <i>et al.</i> 2007); Sur, Alp Flix, Salategnas, 1960 m [46°31'11.00'' N, 9°38'46.00'' E], 1♂ 21.v.–24.vi.2005, pitfall trap, in spruce forest, leg. P. Muff, det. H. Frick (MHNG) (Muff <i>et al.</i> 2007); Sur, Alp Flix, Salategnas, 1960 m [46°31'11.50'' N, 9°38'41.89'' E], 1♂ 17.x.2005 – 06.v.2005, pitfall traps, in spruce forest, leg. P. Muff, det. H. Frick (NMB 2795b) (Muff <i>et al.</i> 2007); Sur, Alp Flix, Salategnas, 1960 m [46°31'11.00'' N, 9°38'46.00'' E], 1♀ 17.x.2005 – 06.v.2006, pitfall traps, in spruce forest, leg. P. Muff, det. H. Frick (NMB 2795a) (Muff <i>et al.</i> 2007); Sur, Alp Flix, Salategnas, 1960 m [46°31'11.50'' N, 9°38'41.89'' E], 1♂ 17.x.2005 – 06.v.2005, pitfall traps, in spruce forest, leg. P. Muff, det. H. Frick (SMF) (Muff <i>et al.</i> 2007); Sur, Alp Flix, Salategnas, 1960 m [46°31'09.24'' N, 9°38'47.74'' E], 1♀ 19.ix.-16.x.2005, pitfall trap, alpine timberline, leg. P. Muff, det. H. Frick (SMF) (Muff <i>et al.</i> 2007).</p> <p> <b>Examined material. Austria:</b> <i>Vorarlberg</i>: Montafon, Garneratal, close to Gaschurn, 1560 m [46°57'56'' N, 10°00'40'' E], 1♂ 19.vii.–29.viii.2000, leg., det. and coll. W. Breuss (Breuss unpubl.). <b>France:</b> <i>Rhône- Alpes</i>: Haute-Savoie, Chamonix, montagne des Posettes (Montroc), 1600 m [45°59'40'' N, 6°56'03'' E], 1♀ 18.viii.1993, spruce forest with some birch trees, ground dwelling, leg., det. and coll. J.-C. Ledoux (Ledoux unpubl.); Vallorcine, entrance to the canyon of Bérard, 1680 m [46°02'30'' N, 6°56'10'' E], 1♂ 17.viii.1993, underbrush of larch trees, in litter, leg., det. and coll. J.-C. Ledoux (Ledoux unpubl.). <i>Provence-Alpes-Côte d’Azur</i>: Alpes-de-Haute-Provence, Banon, ca. 800 m [44°02'16'' N, 5°37'40'' E], 1♂ 11.v.1986, leg. P. Poot, det. and coll. R. Bosmans (Bosmans unpubl.); Hautes-Alpes, Ceillac, ca. 1650 m [44°40'03'' N, 6°46'39'' E], 1♀ 04.viii.1980, leg. P. Poot, det. and coll. R. Bosmans (Bosmans unpubl.). <b>Switzerland:</b> <i>Bern</i>: Axalp, 1550 m [46°43'00'' N, 8°02'20'' E], 1♂ vi., leg. R. de Lessert, det. H. Frick (MHNG) (Lessert 1907). <i>Grisons</i>: Sur, Alp Flix, Salategnas, 1960 m [46°31'11.50'' N, 9°38'41.89'' E], 3♂ 17.x.2005 – 06.v.2005, pitfall traps, in spruce forest, leg. P. Muff, det. H. Frick (NMBE AR 6740) (Muff <i>et al.</i> 2007); Sur, Alp Flix, Salategnas, 1960 m [46°31'11.00'' N, 9°38'46.00'' E], 1♂ 21.v.–24.vi.2005, pitfall trap, in spruce forest, leg. P. Muff, det. H. Frick (coll. H. Frick, SP _0362) (Muff <i>et al.</i> 2007); Sur, Alp Flix, Salategnas, 1960 m [46°31'11.00'' N, 9°38'46.00'' E], 1♀ 17.x.2005 – 06.v.2006, pitfall traps, in spruce forest, leg. P. Muff, det. H. Frick (coll. H. Frick, SP _0363) (Muff <i>et al.</i> 2007); Trins, Mulins, above Purcs, ca. 1800 m [46°50'42.32'' N, 9°21'11.41'' E], 1♂ 2♀ 01.viii.1930, leg. E. Schenkel, det. P. Muff (NMB 2795f) (Schenkel 1933); Trins, Mulins, Bargis–Rischiglus–Furca–Flimserstein [46°51'30'' N, 9°17'30'' E], 1♀ 11.viii.1930, alpine zone, leg. E. Schenkel, det. P. Muff (NMB 2795f) (Schenkel 1933); Trins, Mulins, Belmont–Bargis, ca. 1550–2000 m [46°51'10'' N, 9°18'40'' E], 1♀ 21.vii.1930, leg. E. Schenkel, det. P. Muff (NMB 2795f) (Schenkel 1933); Trins, Mulins, below Alp Mora, ca. 1800 m [46°50'44'' N, 9°21'10'' E], 1♂ 2♀ 11.viii.1931, upper forest part, leg. E. Schenkel, det. P. Muff (NMB 2795f) (Schenkel 1933); Trins, Mulins, Si Munt-Uaul Sec, ca. 1200 m [46°50'0'' N, 9°21'10'' E], 1♂ 1♀ 04viii.1930, leg. E. Schenkel, det. P. Muff (NMB 2795f) (Schenkel 1933). <i>Nidwalden</i>: Bruniswaldalp close to Altzellen,> 1400 m [46°51'20'' N, 8°23'20'' E], 1♂ 4♀ viii., leg. E. Schenkel, det. P. Muff (NMB 2795g) (Schenkel 1923). <i>Ticino</i>: Val Bedretto, Bedretto to Alpe di Folcra, 1400–1800 m [46°30'8'' N, 8°30'59'' E], 1♀ 11.–22.vii.1927 /1928, forest slope on the right valley side, leg. E. Schenkel, det. P. Muff (NMB 2795e) (Schenkel 1929). <i>Valais</i>: close to Fiesch, Rafgarten – Ober Titer, 1500 m – 1600 m [46°30'50'' N, 8°18'20'' E], 6♀ 15.vii.1925, leg. E. Schenkel, det. P. Muff (NMB 2795c) (Schenkel 1926); Fionnay, 1500 m [46°01'54'' N, 7°18'26'' E], 1♂ 2♀ ix.1906, in moss of spruce forest, leg. R. de Lessert, det. H. Frick (MHNG) (Lessert 1907; Thaler 1972); Leukerbad, ca. 1400 m [46°22'30'' N, 7°37'30'' E], 1♂ 4♀ viii.1930, leg. R. de Lessert, det. H. Frick (MHNG), 1♂ 1♀ viii.1930, leg. R. de Lessert, det. P. Muff (NMB 2795h) (Lessert 1930); Lötschental, close to Ried, 1500 m – 1600 m [46°24'50'' N, 7°48'20'' E], 1♂ 11♀ vii.1938, leg. E. Schenkel, det. P. Muff (NMB 2795i) (Schenkel 1939); Saas-Tal, Saas-Tal below Saas-Fee, Almagell–Saas-Fee, ca. 1600 m [46°06'30'' N, 7°55'40'' E], 1♂ vii./viii., leg. E. Schenkel, det. P. Muff (NMB 810d) (Schenkel unpubl.).</p> <p> <b>Diagnosis.</b> <i>C. zamoniensis</i> spec. nov. is most similar to <i>C. avicula</i> but differs in the shape of the male and female genitalia and the shape of the male cephalic lobe.</p> <p> <i>Males</i>: Cephalic lobe of <i>C. zamoniensis</i> spec. nov. more robust than in <i>C. avicula</i>: the neck-like prolongation of <i>C. zamoniensis</i> spec. nov. is of equal diameter directly below and above the eye-field (AME, ALE, PLE) (Fig. 54) but much thinner below the eye-field in <i>C. avicula</i> (Fig. 23); distance between sulcus and AME is below 0.11 mm in <i>C. zamoniensis</i> spec. nov. (Fig. 53) and above 0.12 mm in <i>C. avicula</i> (Fig. 22); sulcus cup-like in <i>C. zamoniensis</i> spec. nov. and channel-like in <i>C. avicula</i>. Embolus of <i>C. zamoniensis</i> spec. nov. short, broad and robust basally, thin and U-shaped distally (Figs 49, 50); <i>C. avicula</i> with long, straight and whip-like embolus that narrows constantly towards the end (Figs 18, 19). <i>C. zamoniensis</i> spec. nov. tibia I proximally bent and dorsally with glabrous area on the proximal half (Fig. 55) and no macroseta, in <i>C. avicula</i> with one dorsal macroseta in small glabrous field (Fig. 24).</p> <p> <i>Females</i>: Epigyne of <i>C. zamoniensis</i> spec. nov. with two anterior pouches formed by the ventral and dorsal plate, anterior borders highly sclerotised (Fig. 56). Pouches in <i>C. avicula</i> much larger and less sclerotised (Fig. 26). <i>C. zamoniensis</i> spec. nov. with ventrally visible square dorsal plate, sclerotised parts of the vulva visible in transparency through ventral and dorsal plate defining a bright hourglass-like form centrally (Fig. 56). <i>C. avicula</i> with rectangular dorsal plate without sclerotised parts visible in transparency through dorsal plate but lateral to it (Fig. 26). Vulva of <i>C. zamoniensis</i> spec. nov. without copulatory duct, those of <i>C. avicula</i> with. Vulva of <i>C. zamoniensis</i> spec. nov. simple with hook-like sclerotised pouch borders, originating anterior and mesal to the receptacula (Figs 57, 58), in <i>C. avicula</i> shapes more complex (Figs 27, 28).</p> <p> <b> Description. <i>Male</i></b> (Holotype, NMBE Ar 6741): Total length 2.18 mm. Cephalothorax: honey brown (138 U); reticulated; broad oval; 0.85 mm long without cephalic lobe (Fig. 54), 1.22 mm long with cephalic lobe (Fig. 54); 0.65 mm wide. Cephalic lobe: honey brown (138 U); shaft with few long hairs (Fig. 52); shaft constantly thick, at thinnest part below the eye-field 0.10 mm wide laterally, 0.11 mm wide dorsally (Figs 52, 54); tip of lobe laterally flattened with many short, stout and few long, slender hairs anterior to the PME (Figs 52, 54); sulcus 0.08 mm below AME (Fig. 53). Eyes: PME topmost on the cephalic lobe; AME projecting forward, lateral eyes besides the AME; one long macroseta projecting forward between AME (Fig. 54). Clypeus: directed obliquely backwards. Sternum: very fine brown (469 U) pigmentation on yellow (124 U) ground, dark brown (469 U) on the margins; 0.47 mm long; 0.51 mm wide; shield-shaped. Chelicerae: yellow (124 U); promargin with 5 teeth; retromargin with 5 denticles; stridulatory striae very dense and fine. Legs: yellow to light brown (120 U); formula 4-1-2-3; tibia I proximally bent and dorsal with glabrous area from proximal to more than half its length (Fig. 55), tibia III–IV with one dorsal proximal macroseta (0-0-1-1); metatarsi I–III with one trichobothrium, Tm I: 0.54 mm, metatarsus IV without trichobothria. Pedipalp: patella two times longer than broad, tibia retrolateral with expansion (round glabrous area, Fig. 51), one retrolateral and one prolateral trichobothrium (Fig. 51); paracymbium a simple clasp; tegulum distal with short and long papillae on protegulum (Fig. 48); suprategular apophysis semi-circular; marginal suprategular apophysis rather small, emerging close to the tip; distal suprategular apophysis robust, highly sclerotised (Figs 49, 50); column broad; embolic membrane slender; radix simple without any processes other than the elongated radical tailpiece and the embolus; embolus strongly sclerotised, twisted; broad at the base; very thin, curved tip (Fig. 50). Abdomen: dark olive green-brown (125 U); booklung covers very light brown (467 U); scaly.</p> <p> <i>Female</i> (Paratype, NMBE Ar 6742): Total length 1.81 mm. Cephalothorax: honey brown (138 U); reticulated; 0.89 mm long; 0.65 mm wide. Eyes: posterior row slightly procurved; anterior row straight. Sternum: very fine brown (469 U) pigmentation on yellow (124 U) ground, dark brown (469 U) on the margins; 0.46 mm long; 0.46 mm wide; shield-shaped. Chelicerae: honey brown (138 U); promargin with 5 large teeth; retromargin with 5 denticles; stridulatory striae very fine and dense. Legs: yellow (122 U); formula 4-1-2-3; tibia I–IV with one dorsal proximal macroseta (1-1-1-1); metatarsi I–III with one trichobothrium, Tm I: 0.52 mm, metatarsus IV without trichobothria. Epigyne: simple with hook-like sclerotised pouch borders, originating anteriorly and mesally to the receptacula (Figs. 57, 58); dorsal plate square, fully visible in ventral view; sclerotised parts of vulva visible in transparency through ventral and dorsal plate, defining a bright hourglass-like form centrally (Fig. 56). Vulva: without copulatory duct; receptacula globular, incoming dorsally. Abdomen: dorsal olive green-brown (119 U), ventral darker (147 U).</p> <p> <b>Variation</b>. The measurements are based on all type material (10♂ 9♀) plus specimens from the NMB (810i: 1♂ 2♀) and the MHNG (Axalp: 1♂; Fionnay: 1♂ 1♀).</p> <p> <i>Males</i> (n=13, means in brackets): The coloration is variable. Total length 1.91–2.18 mm (2.09 mm). Cephalothorax: 0.73–0.86 mm (0.82 mm) long without cephalic lobe, 1.10–1.23 mm (1.18 mm) long with cephalic lobe; 0.61–0.69 mm (0.65 mm) wide. Cephalic lobe: at thinnest part below the eye-field 0.10–0.13 mm (0.11 mm) wide laterally, 0.09–0.11 mm (0.11 mm) wide dorsally; sulcus 0.07–0.11 mm (0.08 mm) below AME (Fig. 53). Legs: Tm I: 0.50–0.59 mm (0.54 mm).</p> <p> <i>Females</i> (n=12, means in brackets): The colorations are variable. Total length 1.62–2.00 mm (1.82 mm). Cephalothorax: 0.75–0.89 mm (0.82 mm) long; 0.60–0.65 mm (0.62 mm) wide. Legs: Tm I: 0.48–0.60 mm (0.53 mm).</p> <p> <b>Distribution.</b> Endemic to the Alps, occurring in the Western- and Central Alps in France, Switzerland and Austria (Fig. 59). The Eastern distribution border seems to be in Western Austria. Checking of specimens of <i>C. avicula</i> collected west of Vorarlberg (Austria) revealed no misidentifications.</p> <p> <b>Habitat.</b> <i>C. zamoniensis</i> spec. nov. occurs in the litter layer of Norway spruce (<i>Picea abies</i>) forests at the alpine timberline. Most sampling sites were inside the forest with no direct sunlight under branches of Norway spruce. The collection site and its surroundings were sampled intensively in two previous studies (Frick <i>et al.</i> 2006; Frick <i>et al.</i> 2007; Muff <i>et al.</i> 2007). We found no specimens of <i>C. zamoniensis</i> spec. nov. around stand alone trees in the dwarf-shrub heath with a similar microclimate as the closed forests. <i>C. zamoniensis</i> spec. nov. seems to avoid the open land. We only found two specimens in more open areas in the dwarf-shrub heath close to the subalpine forest. <i>C. zamoniensis</i> spec. nov. was never collected together with <i>C. avicula</i> in the same pitfall trap but already in pitfall traps about 20 m away from <i>C. avicula</i>. The locus typicus is approximately 50 m away from the alpine timberline in the subalpine deciduous forest. We found the type specimens in litter under snow close to the tree trunk under a Norway spruce (Fig. 47) at 1960 m a.s.l. Other specimens were found between 1400–2000 m in litter and moss of spruce forests (e.g. Schenkel 1939). One record was much lower at app. 800 m in France (Bosmans pers. comm.).</p> <p> <b>Phenology.</b> This species seems to be eurychronous. All records of other authors at altitudes from 1400 m to 1800 m were between July and September. However, at the type locality (1960 m) specimens were exclusively found between September and June. This corresponds with the time between the first snow fall and the beginning of the snow free time.</p> <p> <b>Etymology.</b> The cephalic lobe of the male is morphologically very similar to the noses of the so called dwarf pirates and other imaginary figures from “Zamonia”. Zamonia is a continent inhabited by freaky creatures in the novel “The 13 ½ Lives of Captain Bluebear” by the German writer Walter Moers (2000). Translated, the species name means “ <i>Caracladus</i> from Zamonia”.</p> <p> <b>Remarks.</b> <i>C. zamoniensis</i> spec. nov. lacks a copulatory duct. The insertion of sperm is assumed to take place through a space between the ventral and the dorsal plates which are supposed to be pressed apart during copulation.</p> <p> The specimens that Lessert (1907, 1910) shows have been evaluated by H.F. The figures of males in Lessert (1907: figs 5, 6) and reprinted in Lessert (1910: figs 98, 99) show <i>C. zamoniensis</i> spec. nov. and not <i>C.</i></p> <p> <i>avicula</i>. The female mentioned in Lessert (1907: fig. 7) and Lessert (1910: fig. 100) shows <i>Diplocentria bidentata</i> (Emerton, 1882) (Thaler 1972).</p> <p> The specimen that was pictured by Pesarini (1996: figs 9–10) was not available to the authors. A definite assignment to either <i>C. avicula</i> or <i>C. zamoniensis</i> spec. nov. is not possible. However, his records are referred to as <i>C. avicula</i> in the distribution map (Fig. 59) and the list of records.</p> <p> The remaining pictures so far named as <i>C. avicula</i> in Heimer and Nentwig (1991: figs 350.1–350.5), Millidge (1977: fig. 162), Simon (1884: figs 408, 409 and fig. 8 on plate 27) and Thaler (1969: figs 16–21, 1972: figs 7–11) are correctly assigned to <i>C. avicula</i>.</p>Published as part of <i>Frick, Holger & Muff, Patrick, 2009, Revision of the genus Caracladus with the description of Caracladus zamoniensis spec. nov. (Araneae, Linyphiidae, Erigoninae), pp. 1-37 in Zootaxa 1982</i> on pages 20-26, DOI: <a href="http://zenodo.org/record/185321">10.5281/zenodo.185321</a>
Remarks by Robert H. Frick
No full textIt is impossible in a reasonable space of time to cover the changes that have occurred in relationships between host countries and oil companies since the first concession agreements in the early 1900’s. It is difficult to cover even the developments of the past three years. Oil producing countries have, of course, always wanted a greater share of the profits from producing operations within their borders and to exercise a greater control over such operations. With the use of hindsight it is possible to say that the degree to which these twin goals have been achieved over the past few years is not remarkable. I believe it is true, however, that five or even three years ago very few, if any, in the petroleum industry would have forecast the success which the producing countries have achieved.</jats:p
Afroneta sarahae Frick & Scharff 2018, sp. nov.
No full text<i>Afroneta sarahae</i> sp. nov. <p>urn:lsid:zoobank.org:act:ACC8A04A-41EE-489B-B929-3912135333E2</p> <p>Figs 11D–F, 12–13</p> Diagnosis <p> The presence of serrations on the ventral margin of the paracymbium is seen in only one more species, <i>Afroneta serrata</i> sp. nov. The shape of the serrations is variable (see Fig. 13B–E), ranging from many shallow fine denticles to a few deep strong teeth. The tegular mynoglenine process is roundish and smaller compared to what is seen in <i>Afroneta serrata</i> sp. nov. The radix is situated in the distal half of the cymbium (Fig. 13F) and is shorter than in <i>Afroneta serrata</i> sp. nov. (Fig. 9C). The copulatory duct in females is correspondingly shorter (Fig. 12G–H) than in <i>Afroneta serrata</i> sp. nov. (Fig. 10G–H) and the dorsal plate with the dorsal plate scape is also narrower in its longitudinal dimension (Fig. 9D vs Fig. 13G).</p> Etymology <p> The species epithet <i>sarahae</i> is a name in apposition. It refers to Holger Frick’s partner, Sarah Küffer, who has supported Holger Frick’s passion for spiders for more than a decade.</p> Type material <p> <b>Holotype</b></p> <p> KENYA: ♂, Rift Valley Prov., Trans-Nzoia Distr., Mount Elgon National Park, upper course of Kimothon Riv., 1°5 <i>′</i> 53.1 <i>″</i> N, 34°37 <i>′</i> 13.7 <i>″</i> E [WGS84], 3645 m a.s.l., 19 Jan. 2009, N. Yunakov leg., H. Frick det., collection Natural History Museum of Oslo (sample KE005, ZMUN 24056).</p> <p> <b>Allotype</b></p> <p>KENYA: ♀, same data as for holotype (ZMUN 24056).</p> <p> <b>Other material examined</b> (1 ♂, 7 ♀♀)</p> <p>KENYA: 1 ♂, 7 ♀♀, together with holotype, collection Natural History Museum of Oslo (sample KE005, ZMUN 24056).</p> Description <p> <b>Male</b> (holotype, ZMUN 24056)</p> <p>SIZE. Total length 1.88. Cephalothorax 1.06 long, 0.76 wide. Sternum 0.59 long (0.54 without labium), 0.53 wide. Abdomen 0.91 long, 0.72 wide. AME diameter 0.04. Femur I 0.79 long, 0.75 times as long as cephalothorax.</p> <p>COLOUR (preserved specimens, Fig. 11D, F). Cephalothorax and chelicerae brownish, sternum darker and with blackish-grey margin. Legs and pedipalps yellowish white, without annulations. Black rings around eyes. Abdomen dark grey, with white markings. Figure 11D–F illustrates recently collected material (2009), stored in 96% ethanol. The colour is probably close to the colour of the live animals.</p> <p> BODY. Cephalothorax with short pale setae in the midline. No fovea (Fig. 11F). Ocular area without setae between eyes. Clypeus height 4 times AME diameter. Subocular sulci present below ALE, clearly demarcated, longer than wide and narrow (Fig. 11D). Cephalothorax more elongated and narrower (Fig. 11E–F) as compared to <i>Afroneta serrata</i> sp. nov. (Fig. 11B–C).</p> <p>CHELICERAE. With 3 large widely spaced prolateral teeth (Fig. 11D). Without stridulating file. Three small closely spaced retrolateral denticles, positioned between the two first prolateral teeth.</p> <p>LEGS. All femora with short thin setae dorsally and ventrally. Ventral setae shorter than diameter of femora. Leg formula 1243. Trichobothrium metatarsus I = 0.37 (0.41 on other male specimen in vial). No tibial spines.</p> <p> PEDIPALP (Figs 12A–D, 13A–F). Patella with long strong macrosetae (Fig. 12A). Tibia with two retrolateral and one prolateral trichobothrium (Fig. 12D). Cymbium with two prolateral macrosetae (Fig. 13A). Paracymbium J-shaped, with unusual distal serrations on ventral margin (Fig. 13A–F). It holds two basal setae (Fig. 13A) and its distal part is well set off from the cymbium in dorsal view (Fig. 12D). Suprategulum narrow and triangular. Tegular mynoglenine process short and roundish (Figs 12A, 13A), smaller than in <i>Afroneta serrata</i> sp. nov. (Figs 9A, 10A). Radical division small restricted to distal half of alveolus (Fig. 13F). Radix drop-like. Embolus with broad base, robust and almost straight and tapering towards the tip (Figs 12C, 13C). Embolic membrane exceeding the embolus and the alveolus only slightly (Fig. 13F), less than in <i>Afroneta serrata</i> sp. nov.</p> <p> <b>Female</b> (allotype, ZMUN 24056)</p> <p>SIZE. Total length 2.41 (abdomen strongly bent downwards so total length difficult to measure). Cephalothorax 1.44 long, 0.96 wide. Sternum 0.79 long (0.71 without labium), 0.63 wide. Abdomen 1.32 long, 0.91 wide. AME diameter 0.06. Femur I 1.00 long, 0.71 times as long as cephalothorax.</p> <p>COLOUR (preserved specimen, Fig. 11E). As holotype.</p> <p>BODY. Sternum shield–shaped. Clypeus height 3.5 times AME diameter.</p> <p>CHELICERAE. With 3 large widely spaced prolateral teeth. Retrolateral denticles not visible. Chelicerae without stridulating file.</p> <p>LEGS. Spination of legs like male. Leg formula 1243. Trichobothrium metatarsus I = 0.47.</p> <p>EPIGYNUM AND VULVA (Figs 12E–H, 13G–H). The epigyne has a dorsal plate scape that is moderately developed and neither extends much ventrally nor posteriorly (Fig. 12E–F). The copulatory ducts expand anteriorly as far as the receptacula and are separated from each other by less than their diameter (Fig. 12G–H). The receptacula are round.</p> Distribution <p>Only know from Mount Elgon, Kenya, at altitudes of 3700 m a.s.l.</p> Life history <p>Little is known about the biology of this species. Specimens have been collected in the alpine belt above the forest zone.</p>Published as part of <i>Frick, Holger & Scharff, Nikolaj, 2018, Description of one new genus and four new species of mynoglenine spiders from Africa (Araneae: Linyphiidae: Mynogleninae), pp. 1-27 in European Journal of Taxonomy 415</i> on pages 20-24, DOI: 10.5852/ejt.2018.415, <a href="http://zenodo.org/record/1211253">http://zenodo.org/record/1211253</a>
Stenocephalemys albocaudata Frick 1914
No full textStenocephalemys albocaudata Frick, 1914. Ann. Carnegie Mus., 9:8. TYPE LOCALITY: Ethiopia, Chilalo Mtns., Inyala Camp. DISTRIBUTION: Ethiopia. ISIS NUMBER: 5301410011061001001.Published as part of James H. Honacki, Kenneth E. Kinman & James W. Koeppl, 1982, Order Rodentia (Part 5), pp. 504-560 in Mammal Species of the World (1 st Edition), Lawrence, Kansas, USA :Alien Press, Inc. & The Association of Systematics Collections on page 556, DOI: 10.5281/zenodo.735303
[H. C. Frick Coke Co., Engine Drawing Card, Sketch No. 5031]
No full textThis engine drawing card was created for H. C. Frick Coke Company, Class 4-10 C. Section N-4C. Sketch 5031. Copy Spec. B2979 - B3318
Stenocephalemys Frick 1914
No full textStenocephalemys Frick, 1914. Ann. Carnegie Mus., 9:7. REVIEWED BY: D. A. Schütter (DS); E. Van der Straeten (EVS). COMMENT: Reviewed by Yalden et al., 1976, Monitore Zool. Ital., n.s., suppl. 8(l):39-40, and Rupp, 1980, Saugetierk. Mitt., 28:81-123. ISIS NUMBER: 5301410011061000000.Published as part of James H. Honacki, Kenneth E. Kinman & James W. Koeppl, 1982, Order Rodentia (Part 5), pp. 504-560 in Mammal Species of the World (1 st Edition), Lawrence, Kansas, USA :Alien Press, Inc. & The Association of Systematics Collections on pages 555-556, DOI: 10.5281/zenodo.735303
Purine cyclic nucleotides and EGF cooperatively stimulate neonatal rat hepatocyte growth in primary tissue culture
No full textPurine cyclic nucleotides and EGF cooperatively stimulate neonatal rat hepatocyte growth in primary tissue cultur
Instructions générales en forme de catechisme ...
No full textSign.: a\p4\s, A-P\p12\s, b-g\p12\s, h\p6\sGrab. xil. en la por
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