Lichens A-Pac (2007) - Flora of New Zealand Lichens - Revised Second Edition A-Pac
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Buellia De Not.

BUELLIA De Not., 1846  nom. cons. 

=HAFELLIA Kalb, H.Mayrhofer & Scheid., 1986

Type: Buellia disciformis (Fr.) Mudd,  typ. cons.  [=Lecidea parasema var. disciformis Fr.]

Type : Hafellia parastata (Nyl.) Kalb, H.Mayrhofer & Scheid.  Lecidea parastata Nyl.]

Description : Flora (1985: 44). See also Orange, Coppins & Scheidegger in Purvis et al. (1992: 129–130) and Foucard et al. (2002: 11–25). Ascomata apothecia, cryptolecanorine (completely immersed in thallus and without an exciple), lecanorine, biatorine and lecideine. Exciple aethalea -type, vilis -type, dispersa -type and leptocline -type (Scheidegger 1993). Asci (4–)8(–many)-spored, clavate, 30–100 μm, Bacidia -type (Malcolm & Galloway 1997: 186). Ascospores brown, 1-septate, rarely 3-septate or submuriform, ellipsoidal, oblong or fusiform, straight or curved; wall is of uniform thickness (Buellia -type) consisting of four layers – the outermost layer, W1, is faintly pigmented, W2 is uncoloured and W3 is pigmented with greater intensity than W1. These three layers are very thin and are only easily seen after pretreatment of spores with K. The innermost layer, W4, is uncoloured and distinctly thicker than all the outer layers (Scheidegger 1993). Sometimes ascospores also with median (Physconia -type) or subapical (Callispora -type) thickenings. Outer spore wall smooth (psilate) or finely ornamented (striate, microrugulate, rugulate or microfoveate), seen under oil immersion. Conidiomata pycnidia immersed. Conidiophores Anaptychia -type. Conidia bacillar 10 × 0.7–1 μm.

Key

1
Saxicolous
2
Corticolous or lignicolous
11
2
Thallus continuous or areolate
3
Thallus effuse-arachnoid, obsolete
3
Apothecial disc pruinose
4
Apothecial disc epruinose
6
4
On acid rocks
5
On basic rocks (limestone, basic sandstone etc.)
5
Thallus ±continuous, white, tartareous, on a pale, grey-black prothallus; medulla I+ violet; apothecia white-pruinose; ascospores 10–16.5 × 4.5–6 μm
Thallus effuse, of pustular-verruciform areolae, yellowish-buff or ochraceous; without a marginal prothallus; medulla I−; apothecia grey-pruinose; ascospores 14–16 × 8–9 μm
6
Thallus K+ yellow or K−
7
Thallus K+ yellow→red (norstictic acid)
7
Thallus K−
8
Thallus K+ yellow (atranorin, confluentic and 2'- O- methylperlatolic acids)
8
Prothallus not stellate-fimbriate
9
Prothallus stellate-fimbriate, resembling Cystocoleus
9
Thallus grey-white, reddish brown or olivaceous; C−
10
Thallus yellowish; C+ orange
10
Hypothecium brown-black
11
Hypothecium pale-brown
11
Thallus grey-white; ascospores fabiform, 11–13 × 5–6 μm
Thallus reddish brown to olivaceous; ascospores ellipsoidal, 12–15 × 6–7 μm
12
Corticolous
13
Lignicolous; thallus effuse or lacking
13
Not sorediate
14
Sorediate
14
Ascospores 8 per ascus; to 30(–40) μm long
15
Ascospores 4 per ascus; (28–)32–42(–50) × 14–18(–22) μm
15
Ascospores with slight subapical wall thickenings; 14–30 × 6–13 μm
Ascospores with marked subapical wall thickenings; (22–)25–30(–40) × (9–)10–12(–14) μm

Buellia, included in the family Physciaceae nom. cons. (Eriksson et al. 2004; Pennycook & Galloway 2004; Eriksson 2005), is a large, cosmopolitan genus of c. 400 species (Kirk et al. 2001) that is, with few exceptions, still very poorly known and collected outside of the Northern Hemisphere, where most recent systematic work has been done. European saxicolous species are discussed by Scheidegger (1993) who gives much useful information on the genus. Corticolous and lignicolous species from the Iberian Peninsula are treated by Giralt et al. (2000a), and Scandinavian taxa by Foucard et al. (2002). The taxonomy and phylogeny of species of Buellia with pluriseptate ascospores is discussed by Anders Nordin (Nordin 1996, 1997, 1999, 2000; Nordin et al. 1999; Nordin & Mattsson 2001). There is an extensive literature on Buellia, especially relating to Northern Hemisphere taxa and populations [see Imshaug (1951); Sheard (1964, 1992 – as Hafellia); Lamb (1968); Hafellner (1979); Bellemère & Letrouit-Galinou (1987); Scheidegger & Ruef (1988); Scheidegger (1993); Rambold et al. (1994); Nordin (1996, 1999, 2000); Kalb & Elix (1998); Moberg et al. (1999); Giralt & Llimona (2000); Giralt et al. (2000a); Grube & (Arup 2001); Trinkhaus et al. (2001); Foucard et al. (2002); Giralt & Nordin (2002), Bungartz (2004); Bungartz & Nash (2004a, 2004b); Bungartz et al. (2004a, 2004b); Grube et al. (2004d)]. In a recent account of corticolous and lignicolous tropical and subtropical species of Buellia s. lat., Marbach (2000) explored a more natural systematic concept based on anatomy, morphology, chemistry and ecology recording as independent segregate genera: Amandinea (q.v.), Baculifera Marbach & Kalb, Chrismofulvea Marbach,  Ciposia Marbach,  Cratiria Marbach,  Endohyalina Marbach,  Fluctua Marbach,  Gassicurtia Fée,  Hafellia Kalb, Marbach & Scheidegger,  Hypoflavia Marbach,  Sculptolumina Marbach,  Stigmatochroma Marbach, and Tetramelas Norman (q.v.). Typification of Buellia is still unequivocally established. The question is discussed by Kalb & Elix (1998: 478–479), who select Buellia parasema De Not. as lectotype; by Moberg et al. (1999), who propose conserving Buellia with Buellia aethalea (Ach.) Th.Fr. as a neotype; and by Nordin (2000). Presently, Buellia De Not.  nom. cons. is typified by Buellia disciformis (Fr.) Mudd,  typ. cons. (Greuter et al. 2000: 178; see also Gams 2004). This view is adopted here.

Buellia is still much in need of collection and revision in New Zealand. Of the 18 taxa discussed in the Flora (Galloway 1985a) several are located elsewhere. B. litoralis is referable to Amandinea lecideina, B. nitrophila is referable to Rinodina otagensis, and B. punctata is referable to Amandinea punctata. Sixteen species are treated here.

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