410 research outputs found
Präsentation Dresdner Forschung in Oxford
Kevin Künzl und Jan Heilmann haben bei der XVIII. International Conference on Patristic Studies in Oxford Ergebnisse ihrer Forschung vorgestellt. Kevin Künzl hat zum Thema "Adopting Teaching as Eating and Drinking: Origen, 'Spiritualizing tendencies', and the Last Supper" vorgetragen. Er hat exemplarisch Stellen, die sonst als Referenz auf "die Eucharistie" verstanden werden, vor dem Hintergrund der konzeptuellen Metapher IDEAS ARE FOOD interpretiert. Auf diese Weise lassen sich die besproch..
Mathematical Psychology
This article appeared originally in 1930, in Dutch, under the title “Mathematiese Psychologie” in Mens en Maatschappij. Translated and annotated by Conrad Heilmann, Stefan Wintein, Ruth Hinz, and Erwin Dekker, it is accompanied—in the present issue—by the article “No Envy: Jan Tinbergen on Fairness” written by Conrad Heilmann and Stefan Wintein
Gründliche Relation Wie es bey Eroberung der Statt Pilsen in Böhmen (so von dem Hoch und Wolgebornen Herrn Graff Ernesten von Mansfeld ... den 11. oder 21. Novemb. 1618. mit stürmender hand eingenom[m]en worden) umbständlich zugangen ...
Erschien ursprüngl. u.d.T.: Heilmann, Johann Jacob: Relatio Historica Pilsnensis, a Statibus Bohemicis Approbat
DS1_JVDI_10.1177_1040638719856655 – Supplemental material for Prospective evaluation of S100A12 and S100A8/A9 (calprotectin) in dogs with sepsis or the systemic inflammatory response syndrome
Supplemental material, DS1_JVDI_10.1177_1040638719856655 for Prospective evaluation of S100A12 and S100A8/A9 (calprotectin) in dogs with sepsis or the systemic inflammatory response syndrome by Brittany E. Thames, James W. Barr, Jan S. Suchodolski, Jörg M. Steiner and Romy M. Heilmann in Journal of Veterinary Diagnostic Investigation</p
Das Davor und das Danach ist wichtiger als der Workshop selbst
Kühl S, Heilmann J, Hermwille A, Nolte M. Das Davor und das Danach ist wichtiger als der Workshop selbst. Wirtschaft und Weiterbildung . 2022;(9):34-37
The safest dependence structure among risks.
In this paper, we investigate the dependence in Frechet spaces containing mutually exclusive risks. It is shown that, under some reasonable assumptions, the safest dependence structure, in the sense of the minimal stop-loss premiums for the aggregate claims involved, is obtained with the Frechet lower bound and precisely corresponds to the mutually exclusive risk of the Frechet space. In that respect, the present paper complements some previous studies by Heilmann (1986), Dhaene & Goovaerts (1996, 1997), Müller (1997) and Taizhong & Zhiqiang (1998). A couple of actuarial applications enhance the interest of the results derived.Dependence; Risk; Structure;
Lactarius dryadophilus Kühner
Lactarius dryadophilus Kühner Lactarius dryadophilus Kühner, 1975a: 68. Holotype: Norway, Hardanger (LY). SYNONYM: Lactarius dryadophilus var. saliceticola Bon and Jamoni in Jamoni and Bon, 1992b: 21. A medium-sized to large, lilac staining Lactarius with cream-coloured, viscid cap with a bearded margin; growing in arctic and alpine areas. DESCRIPTION: Cap 30-100(-150) mm, at first convex with a slightly depressed centre and decurved or inrolled margin, sometimes slightly umbonate; surface sticky, viscid, at the margin bearded and tomentose with up to 2 mm long hairs, whitish chrome to pale cream or warm buff but more brownish in the centre, azonate or slightly zonate. Gills adnate, medium broad, crowded, often forked, whitish to pale cream, later pinkish buff. Stem 20-30 x 15-20 mm, typically curved and tapering downwards; surface whitish to pale cream, sometimes yellowish at the base, very finely pitted or with ochraceous spots, especially towards the base. Flesh firm, becoming hollow in the stem, white, changing to lilac; smell fruity, sweetish; taste mild, like cedar wood to very slightly acrid. Milk white, changing to lilac in contact with the flesh. Spore deposit cream. Spores 9.3-11.8 x 7.2-9.2 um, av. 10.2-10.3 x 8.1-8.4 um, broadly ellipsoid to ellipsoid, Q = 1.15-1.40, av. 1.22-1.27; ornamentation up to 0.3 um high, of rather fine and narrow ridges, often aligned but not forming a reticulum or at most a very incomplete one; isolated warts often elongate; plage inamyloid. Basidia 60-70 x 12-15 um, subclavate, 4-spored. Pleuromacrocystidia moderately abundant, 80-120 x 10-15 um, fusiform, tapering to a mucronate apex. Gill edge sterile; cheilomacrocystidia 40-60 x 7-9 um, fusiform; paracystidia 10-25 x 4-6(-10) um; cylindric to tortuous or clavate. Pileipellis an ixocutis to an ixotrichoderm, 150-200 um thick; hyphae 1-5 um broad, very thin-walled and shrivelled, gelatinized, repent or ascending, some with conspicuous incrustations. ECOLOGY AND DISTRIBUTION: Found in arctic and alpine vegetation types on rich, calcareous soils, often in Dryas-rich grasslands. Rather rare and known from Fennoscandia, the Alps, the Pyrenees and Greenland, and occuring from August to mid September. DISCUSSION: The cap is tomentose only to a short distance from the margin, unlike in L. repraesentaneus, which also has more yellow colours, a longer stem and a different spore ornamentation. The original description of L. groenlandicus was partly based on this species, but recently lectotypified as a synonym of L. pubescens (Knudsen nda Lamoure, 1993).Published as part of Jacob Heilmann-Clausen, Annemieke Verbeken & Jan Vesterholt, 1998, The Genus Lactarius, Copenhagen :Danish Mycological Society on page 10
Lactarius aspideus (FL: Fr. ) Fr.
Lactarius aspideus (FL: Fr.) Fr. Agaricus aspideus Fr.: Fr., 1821: 63; Lactarius aspideus (Fr.: Fr.) Fr., 1838: 336. Type: Not selected; described from Sweden. EXCLUDED: Lactarius aspideus ss. Konrad & Maublanc (= L. flavidus). A small to medium-sized, lilac staining Lactarius wiiln a viscid, straw-yellow to pale cream cap; cap margin finely velutinous in young specimens; growing with Salix. DESCRIPTION: Cap 10-70 mm, at first convex with inrolled margin and slightly depressed centre, then applanate; surface smooth, at margin finely velutinous in young specimens and finely crenulate in older specimens, shiny, viscid to sticky, later almost dry, usually azonate but sometimes with one or a few zones, straw-yellow to pale chrome or pale cream, sometimes with brownish grey watery spots in older specimens, sometimes with lilac tinges. Gills broadly adnate to decurrent, rather narrow, fairly crowded to crowded, rarely forked, whitish chrome to pale cream or cream, turning greyish lilac when bruised. Stem 10-65 X 5-17 mm, cylindric to clavate; surface smooth, greasy, pale straw-yellow to pale cream, not pitted but sometimes with darker yellowish spots, turning greyish lilac when bruised. Flesh rather fragile, solid in the stem, white, slowly turning greyish lilac to pale lilaceous grey when cut, but lilaceous colours disappearing after some hours; smell weak, slightly fruity; taste mild, then becoming bitter. Milk rather abundant, white, unchanging when isolated from the flesh, but drying greyish lilac; taste mild, then bitter and aromatic. Spore deposit pale spores 6.7-9.5 X 5.6-7.8 um, av. 7.8-8.8 X 6.3-7.4 um, subglobose no ellipsoid, Q = 1.05-1.35, av. 1.18-1.24; ornamentation up to 0.5 um high, completely or almost completely reticulate, in a somewhat zebra-like pattern, often with seemingly fissured ridges; isolated warts very rare; plage sometimes slightly amyloid in the distal part. Basidia 35-40 X 9-11 um, cylindric to subclavate, (2- or) 4-spored. Pleuromacrocystidia abundant, fusiform with a moniliform or mucronate apex, 40-65 (~85) x 6-10 um, thin-walled. Gill edge sterile; cheilomacrocysticlia 30-40 x 6-8 um, fusiform to irregularly cylindric, with a moniliform apex; paracystidia 10-25 X 3-6 um, cylindric to subclavate, hyaline and thin-Walled. Pileipellis an ixocutis, 40-70 um thick; hyphae 2-4 um broad, hyaline, repent or slightly ascending. ECOLOGY AND DISTRIBUTION: Found from the end of June to October with Salix in grass or on naked soil in humid localities, often at lake shores. It is Widely distributed but rather uncommon throughout the area.Published as part of Jacob Heilmann-Clausen, Annemieke Verbeken & Jan Vesterholt, 1998, The Genus Lactarius, Copenhagen :Danish Mycological Society on page 9
Erratum: Author Correction: Misestimation of heritability and prediction accuracy of male-pattern baldness (Nature communications (2018) 9 1 (2537))
The original version of this Article contained an error in the spelling of the author Julia Sidorenko, which was incorrectly given as Julia Sirodenko. This has now been corrected in both the PDF and HTML versions of the Article. Further, the sixth sentence of the second paragraph of the Correspondence and the legend to Fig.\ua01 incorrectly omitted citation of work by Heilmann-Helmbach, S. et al. This has now been corrected in both the PDF and HTML versions of the Article
Rhachomyces furcatus Thaxt.
Rhachomyces furcatus (Thaxt.) Thaxt. MB#186405 Figs 17C–D, 102A Proceedings of the American Academy of Arts and Sciences 30: 467 (Thaxter 1895). – Basionym: Acanthomyces furcatus Thaxt., Proceedings of the American Academy of Arts and Sciences 28: 177 (Thaxter 1893) [MB#581133]. – Type: “ On abdomen of Othius fulvipennis Fab., Germany ”; FH. Diagnostic features Thallus variably bent to flexuous. Main receptacle axis continuing into a rather conspicuous lateral branch above the perithecium, even exceeding in length its apex.Appendages type “a” and “b” inseparable, long and very abundant, deeply darkened. Appendages of type “c” consisting of a supporting cell and one antheridium, only visible on the upper lateral branch in mature thalli (Fig. 17D, *). [Detailed descriptions: Thaxter 1896; Santamaria 1989; Majewski 1994b; De Kesel 2002] Distribution and hosts Occurs on species belonging to the genus Othius (Col. Staphylinidae Staphylininae). Known from Europe (Finland, France, Germany, Hungary, Italy, Poland, Romania, Spain, Sweden, United Kingdom, Russia, former Yugoslavia), Africa (Algeria, Uganda), and Asia (Turkey) (Santamaria et al. 1991). More recently it has been recorded from Belgium (De Kesel & Haghebaert 1991), Czech Republic (Rossi & Máca 2006), Denmark (Rostrup 1935), Slovakia (Rossi et al. 2010), the Netherlands (Haelewaters et al. 2012), Armenia, Switzerland, and Bulgaria (Rossi et al. 2019a). Collections examined from Denmark On Othius angustus Stephens, 1833 (Col. Staphylinidae Staphylininae) DENMARK – Nordøstsjaelland (NEZ) • Lille Lyngby Mose; 55°40.831′ N, 12°29.094′ E; UC20; 28 Jan. 2018; J. Søgaard Hansen 999; J. Søgaard Hansen det.; ZMUC C-F-123506. On Othius punctulatus (Goeze, 1777) (Col. Staphylinidae Staphylininae) DENMARK – Østjylland (EJ) • Hald Ege; 56°24.287′ N, 9°20.550′ E; NH25; 19 Oct. 2013; JP 795; JP det.; ZMUC C-F-123290 • Hestehave ved Rønde; 56°17.015′ N, 10°28.162′ E; NH93; 19 May 1994; N. Scharff 391; JP det.; ZMUC C-F-122874 • Kjellerup; 56°17.589′ N, 9°26.117′ E; NH23; 21 Oct. 2017; JP 580; JP det.; ZMUC C-F-123066 • Stidsmølle i Mattrup Skov; 55°55.455′ N, 9°33.811′ E; NG39; 19 Nov. 2017; JP 807; JP det.; ZMUC C-F-123302. – Lolland, Falster, Møn (LFM) • Nyord; 55°2.885′ N, 12°12.380′ E; UB20; 27 Apr. 2013; JP 841; JP det.; ZMUC C-F-123336 • Siesø i Klinteskoven; 54°57.830′ N, 12°32.494′ E; UA49; 15 May 2017; Mo. Hansen DrY0146; Mo. Hansen det.; ZMUC C-F-124214. – Nordøstsjaelland (NEZ) • Gribskov, Faendriksvang; 56°1.005′ N, 12°21.245′ E; UC30; 1–31 May 2014; J. Heilmann-Clausen et al. 49; P. Jørum det.; ZMUC C-F-122524 • ibid.; J. Heilmann-Clausen et al. 163; P. Jørum; ZMUC C-F-122642 • ibid.; 1–30 Jun. 2014; J. Heilmann-Clausen et al. 50; P. Jørum; ZMUC C-F-122525 • Gribskov, Kageruphus; 55°59.428′ N, 12°16.478′ E; UC30; 1–31 May 2014; J. Heilmann-Clausen et al. 47; P. Jørum det.; ZMUC C-F-122522 • ibid.; 55°59.358′ N, 12°16.566′ E; UC30; 1–31 May 2014; J. Heilmann-Clausen et al. 164; P. Jørum det.; ZMUC C-F-122643 • Gribskov, Kalvehave; 56°0.359′ N, 12°20.339′ E; UC30; 1–31 May 2014; J. Heilmann-Clausen et al. 48; P. Jørum det.; ZMUC C-F-122523 • ibid.; J. Heilmann-Clausen et al. 165; P. Jørum det.; ZMUC C-F-122644 • ibid.; 56°0.419′ N, 12°20.564′ E; UC30; 1–31 May 2014; J. Heilmann-Clausen et al. 166; P. Jørum det.; ZMUC C-F-122645 • Gribskov, Kistrupvang; 56°1.612′ N, 12°19.959′ E; UC31; 1–31 May 2014; J. Heilmann-Clausen et al. 167; P. Jørum; ZMUC C-F-122646 • ibid.; 56°1.602′ N, 12°20.048′ E; UC31; 1–31 May 2014; J. Heilmann-Clausen et al. 168; P. Jørum det.; ZMUC C-F-122647 • Gribskov, Nederste Koppel; 56°2.865′ N, 12°19.999′ E; UC31; 1–31 May 2014; J. Heilmann-Clausen et al. 46; P. Jørum det.; ZMUC C-F-122521 • Naerum; 55°49.077′ N, 12°32.686′ E; UB48; 29 Apr. 2017; JP 402; JP det.; ZMUC C-F-122885 • Stampeskov ved Rådvad; 55°48.332′ N, 12°33.138′ E; UB48; 14 Apr. 2013; JP 783; JP det.; ZMUC C-F-123278. – Nordvestsjaelland (NWZ) • Eriksminde syd for Korshage; 55°57.744′ N, 11°46.504′ E; PH70; 27 Oct. 2019; JP 1537; JP det.; ZMUC C-F-124297. – Sydjylland (SJ) • Draved Skov; 55°0.964′ N, 8°58.395′ E; MF99; 1 Jun. 2013; JP 305; JP det.; ZMUC C-F-122784 • Kollund Skov; 54°50.219′ N, 9°25.411′ E; NF27; 8 May 2004; H. Liljehult 79; H. Liljehult det.; ZMUC C-F-122554. – Sydsjaelland (SZ) • Sorø, Kristiansminde; 55°25.115′ N, 11°35.209′ E; PG64; 1–15 Aug. 2013; JP 525; JP det.; ZMUC C-F-123009. On Othius subuliformis Stephens, 1833 (Col. Staphylinidae Staphylininae) DENMARK – Østjylland (EJ) • Grejsdal syd for Hornstrup; 55°44.791′ N, 9°33.051′ E; NG37; 8 Mar. 2014; JP 749; JP det.; ZMUC C-F-123243 • Hald Ege; 56°24.287′ N, 9°20.550′ E; NH25; 19 Oct. 2013; JP 796; JP det.; ZMUC C-F-123291 • Hampen Sø; 56°1.082′ N, 9°23.149′ E; NH20; 21 Mar. 2014; JP 438; JP det.; ZMUC C-F-122923 • Kjellerup; 56°17.589′ N, 9°26.117′ E; NH23; 21 Oct. 2017; JP 581; JP det.; ZMUC C-F-123067 • Stidsmølle i Mattrup Skov; 55°55.455′ N, 9°33.811′ E; NG39; 19 Nov. 2017; JP 808; JP det.; ZMUC C-F-123303 • Tange å vest for Kjellerup; 56°17.959′ N, 9°23.462′ E; NH23; 17 Feb. 2018; JP 988; JP det.; ZMUC C-F-123495 • Vingsted; 55°40.512′ N, 9°23.500′ E; NG27; 6 Oct. 2019; JP 1532; JP det.; ZMUC C-F-124291. – Lolland, Falster, Møn (LFM) • Naesby Strand; 54°44.625′ N, 11°4.539′ E; PF36; 23 Feb. 2014; JP 552; JP det.; ZMUC C-F-123038. – Nordøstjylland (NEJ) • Bøgebakken i Tofte Skov; 56°50.540′ N, 10°11.850′ E; NJ70; 17 May 2013; H. Liljehult 198; JP det.; ZMUC C-F-122677 • Bønderskoven i Tofte Skov; 56°49.955′ N, 10°14.981′ E; NH79; 19 May 2013; JP 314; JP det.; ZMUC C-F-122793 • ibid.; 8–22 Aug. 2013; I. Aggerholm 932; JP det.; ZMUC C-F-123432. – Nordøstsjaelland (NEZ) • Bognaes Storskov; 55°41.242′ N, 12°1.678′ E; UB17; 1 Aug. 2013; JP 362; JP det.; ZMUC C-F-122845 • Gurre Vang; 56°1.470′ N, 12°29.486′ E; UC41; 14 Apr. 2017; JP 270; JP det.; ZMUC C-F-122749 • Stampeskov ved Rådvad; 55°48.332′ N, 12°33.138′ E; UB48; 14 Apr. 2013; JP 784; JP det.; ZMUC C-F-123279. – Nordvestsjaelland (NWZ) • Bognaes Skov på Tuse Naes; 55°44.966′ N, 11°45.817′ E; PG78; 10 Dec. 2013; JP 889; JP det.; ZMUC C-F-123387 • Nordbredden af Skarresø; 55°39.425′ N, 11°22.998′ E; PG47; 19 Feb. 2017; H. Liljehult 366; JP det.; ZMUC C-F-122849 • Sonnerup Skov; 55°56.525′ N, 11°33.988′ E; PH60; 1 Apr. 2017; JP 256; JP det.; ZMUC C-F-122736. – Sydjylland (SJ) • Nord for Vråby Plantage; 55°6.640′ N, 8°30.239′ E; MG60; 21 Apr. 2000; H. Liljehult 199; JP det.; ZMUC C-F-122678. – Sydsjaelland (SZ) • Krobaek i Sjolte Skov; 55°10.772′ N, 12°0.863′ E; UB11; 28 Feb. 2015; JP 444; JP det.; ZMUC C-F-122929. Remarks Perhaps one of the most common species of Laboulbeniales in Denmark, where it is infrequent to find specimens of Othius free of this fungus. Also remarkable is the observation of severely infected hosts.Published as part of Santamaria, Sergi & Pedersen, Jan, 2021, Laboulbeniomycetes (Fungi, Ascomycota) of Denmark, pp. 1-425 in European Journal of Taxonomy 781 on pages 86-89, DOI: 10.5852/ejt.2021.781.1583, http://zenodo.org/record/582892
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