i. Rehydrated stroma. j. Ostiole in section. k. Section of stroma with perithecia. l. Hairs on the surface of mature stroma. m. Stroma surface in face view. n. Subperithecial tissue in section. o, p. Ascospores (o. in cotton blue/lactic acid). q. Asci with ascospores. a, b, p. neotype Scleromyceti Sueciae 303; c, h. WU 24011; d, e, i–o, q. epitype WU

24013, f, g. WU 24015. Scale bars: a, b, g, i = 0.3 mm. c, d, f = 0.5 mm. e, h = 0.8 mm. j, l–n, q = 10 μm, k = 100 μm, o, p = 5 μm ≡ Sphaeria rufa Pers., Obs. Mycol. 1: 20 (1796) : Fr., Syst. Mycol. 2: 335 (1823). Anamorph: Trichoderma learn more viride Pers., Neues Mag. Bot. [Roemer’s] 1: 92 (1794): Fries, Syst. Mycol. 3: 215 (1832). Fig. 19 Fig. 19 Cultures and anamorph of Hypocrea rufa. a–c. Cultures after 12 days at 25°C (a. on CMD; b. on PDA; c. on SNA). PI3K inhibitor d, e. Anamorph on natural substrate showing yellow mycelium. f, g. Conidiation pustules (6 days). h. Conidiophores from shrub (7 days). i–k. Conidiophores from pustule periphery (7–8 days). l. Conidiophore thickenings (10 days). m. Phialides (8 days). n–p. Conidia (7–8 days). f–p. From CMD, 25°C. a–c, f–h, n. CBS 119326. d, e, l. CBS 119325. i–k. C.P.K. 2867. m, o, p. CBS 119327. Scale bars: a–c = 14 mm. d, e = 3 mm. f = 1.5 mm. g = 0.5 mm. h = 50 μm. i, k = 10 μm. j = 15 μm. l–p = 5 μm = Trichoderma lignorum (Tode) Harz, Bull. Soc. Imp. Natur. Moscou 44: 116 (1871). = Trichoderma glaucum E.V. Abbott,

Iowa State Coll. J. Sci.

1: 27 (1927). Stromata when fresh 1–4(–6) mm long, 0.5–1.5 mm high, solitary to gregarious, or aggregated in small numbers or crowded in lines along wood fibres, at first semi-effused, flat, {Selleck Anti-infection Compound Library|Selleck Antiinfection Compound Library|Selleck Anti-infection Compound Library|Selleck Antiinfection Compound Library|Selleckchem Anti-infection Compound Library|Selleckchem Antiinfection Compound Library|Selleckchem Anti-infection Compound Library|Selleckchem Antiinfection Compound Library|Anti-infection Compound Library|Antiinfection Compound Library|Anti-infection Compound Library|Antiinfection Compound Library|Anti-infection Compound Library|Antiinfection Compound Library|Anti-infection Compound Library|Antiinfection Compound Library|Anti-infection Compound Library|Antiinfection Compound Library|Anti-infection Compound Library|Antiinfection Compound Library|Anti-infection Compound Library|Antiinfection Compound Library|Anti-infection Compound Library|Antiinfection Compound Library|Anti-infection Compound Library|Antiinfection Compound Library|buy Anti-infection Compound Library|Anti-infection Compound Library ic50|Anti-infection Compound Library price|Anti-infection Compound Library cost|Anti-infection Compound Library solubility dmso|Anti-infection Compound Library purchase|Anti-infection Compound Library manufacturer|Anti-infection Compound Library research buy|Anti-infection Compound Library order|Anti-infection Compound Library mouse|Anti-infection Compound Library chemical structure|Anti-infection Compound Library mw|Anti-infection Compound Library molecular weight|Anti-infection Compound Library datasheet|Anti-infection Compound Library supplier|Anti-infection Compound Library in vitro|Anti-infection Compound Library cell line|Anti-infection Compound Library concentration|Anti-infection Compound Library nmr|Anti-infection Compound Library in vivo|Anti-infection Compound Library clinical trial|Anti-infection Compound Library cell assay|Anti-infection Compound Library screening|Anti-infection Compound Library high throughput|buy Antiinfection Compound Library|Antiinfection Compound Library ic50|Antiinfection Compound Library price|Antiinfection Compound Library cost|Antiinfection Compound Library solubility dmso|Antiinfection Compound Library purchase|Antiinfection Compound Library manufacturer|Antiinfection Compound Library research buy|Antiinfection Compound Library order|Antiinfection Compound Library chemical structure|Antiinfection Compound Library datasheet|Antiinfection Compound Library supplier|Antiinfection Compound Library in vitro|Antiinfection Compound Library cell line|Antiinfection Compound Library concentration|Antiinfection Compound Library clinical trial|Antiinfection Compound Library cell assay|Antiinfection Compound Library screening|Antiinfection Compound Library high throughput|Anti-infection Compound high throughput screening| velutinous, with white mycelial margin; becoming pulvinate, selleck kinase inhibitor more rarely turbinate or discoid, circular to irregular in outline, broadly attached; margin often becoming free and concolorous with the stroma surface. Surface velutinous, at least when young, smooth, slightly uneven or granular. Ostioles invisible or appearing as watery, hyaline, or indistinct darker dots, less commonly projecting, convex, often irregularly distributed. Stromata at first white, remaining white with yellowish ostiolar dots (“albino” form), or more commonly becoming variably coloured from the centre: first yellowish, then pale ochre, light brownish or yellow-, orange-, rust-brown, 5A4–7, 5B4, 5C6–7, 6CD5–8, later light to dark reddish brown, 7–8CD6–8, 8E7–8, sometimes with whitish to rust-coloured scurf. Stromata when dry (0.5–)0.6–3(–5.7) × (0.4–)0.6–2(–3.4) mm, (0.2–)0.3–0.6(–0.9) mm thick (n = 31), KOH–, darker and surface more uneven than in fresh stromata, surface granular to finely tuberculate, sometimes extremely uneven with perithecial contours visible; ostioles not visible or partly convex or semiglobose, appearing as hyaline or brown dots (30–) 40–85(–126) μm (n = 33) diam, generally hyaline after addition of water.