Lichens A-Pac (2007) - Flora of New Zealand Lichens - Revised Second Edition A-Pac
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Caloplaca Th.Fr.

CALOPLACA Th.Fr., 1860  nom. cons. 

=LEPROPLACA (Nyl.) Hue, 1887  

Type : Caloplaca cerina (Ehrh. ex Hedwig) Th.Fr. [=Lichen cerinus Ehrh. ex Hedwig]

Type : Leproplaca xantholyta (Nyl.) Hue [=Lecanora xantholyta Nyl.]

Description : Flora (1985: 60).

Key

1
Muscicolous or corticolous
2
Saxicolous or terricolous
13
2
Parasitic on living mosses
3
Corticolous
5
3
Apothecia scattered, yellow-brown or orange-yellow, margins glossy, grey to black
4
Apothecia cinnabar-red to brownish orange, margins concolorous with disc, irregular, somewhat swollen, greyish below, excluded in old fruits
4
Apothecial disc orange or orange-yellow, margins grey; ascospores 12–15(–18) × 7–9 μm, septum 5–8 μm thick
Apothecial disc orange-brown, margins black to grey-black; ascospores (15–)17.5–20 (–22.5) × 7.5–9 μm, septum to 2.5 μm thick
5
Thallus sorediate
6
Thallus without soredia
7
6
Thallus greyish, inconspicuous; soralia rounded, orange-yellow; apothecia rare; ascospores (10–)13–20 × 7–10 μm, ellipsoidal, septum 3–5 μm thick
Thallus yellow or greyish yellow, spotted orange (K+ purple), dissolving in a granular-furfuraceous, sorediate crust; apothecia common; ascospores (12–)15–18(–20) × (3.5–)5– 7(–8.2) μm; septum 5–8 μm thick
7
Ascospores 1-septate
8
Ascospores 3(–5)-septate
8
Apothecial discs yellow or orange
9
Apothecial discs rusty red-brown
9
On living bark
10
On lignum (fenceposts, worked wood etc.)
10
Apothecia densely crowded, contiguous to hummocky, minute (0.05–0.3 mm diam.), often obscuring thallus
11
Apothecia scattered, not densely crowded, 0.1–1.5 mm diam.; thallus distinct
12
11
Asci 10–16-spored; ascospores broadly ellipsoidal to oval, 8.5–10(–12) × 5–7 μm; septum 5–6 μm thick
Asci 8-spored
12
Thallus grey-white, granular-scurfy; apothecia sessile, disc orange-red to pale yellowish orange, margins entire to subcrenulate, concolorous with thallus; ascospores broadly ellipsoidal to ovoid, (12–)15–16.5(–18.3) × 6.5–8.5 μm; septum 7–8.5 μm thick
Thallus whitish green to pale greyish or bluish, glossy to matt, continuous to abraded; apothecia immersed at first, erumpent to sessile, disc orange to mustard-yellow, roughened-granular, proper margin grey-black to black; ascospores ellipsoidal to broadly ellipsoidal, (11.5–)13–15(–17) × 6.5–8.2 μm; septum 5–7 μm thick
13
Saxicolous
14
Terricolous; thallus squamulose, with marginal, labriform soralia; occasional to crowded apothecia, the disc orange-brown to red-brown, sometimes with plugs of sterile tissue centrally; and oblong-ellipsoidal ascospores, 11–15(–16.5) × 6.5–8.5 μm; septum 2–3.5 μm thick
14
On basic (calcareous) rocks
15
On acidic rocks
24
15
Thallus subsquamulose, ±radiate-plicate
16
Thallus not subsquamulose or radiate-plicate
17
16
Sorediate
Without soredia
17
Sorediate
18
Without soredia
20
18
Thallus leprose
19
Thallus of dispersed or contiguous sorediate granules
19
Thallus dull brownish yellow, minutely granular or pulverulent; marginal lobes absent
Thallus yellow, pulverulent; marginal lobes present
20
Thallus yellow
21
Thallus grey or immersed
23
21
Apothecia sessile
22
Apothecia urceolate-immersed at first; ascospores12–15 × 5–7 μm, the two end locules connected by a wide canal that divides, becoming 4-loculate when mature
22
Ascospore septum 1–3 μm thick
Ascospore septum 3–5 μm thick
23
Ascospore septum 1–2 μm thick
Ascospore septum 3–5 μm thick
24
Thallus yellow, orange or reddish, K+ purple
25
Thallus grey, white or black, K–
40
25
Thallus dwarf-fruticose, squamulose, plicate-radiate, verrucose or leprose
26
Thallus crustose continuous, areolate or lacking
30
26
Thallus dwarf-fruticose
27
Thallus squamulose, plicate-radiate, verrucose or leprose
28
27
Lobes erect; pseudocyphellae scattered, inconspicuous; alpine
Lobes spreading, not erect; pseudocyphellae prominent; coastal
28
Thallus squamulose, or plicate-radiate
29
Thallus leprose, bright yellow; in alpine to high-alpine underhangs
29
Thallus plicate-radiate at margins; ascospores oval-ellipsoidal apices rounded or pointed, 11.5–13(–15) × 5–7 μm; septum 3–5 μm thick; high-alpine
Thallus squamulose or squamulose-areolate; ascospores oblong-ellipsoidal, apices rounded, (13–)15–16.5(–18.3) × 6.5–10 μm; septum 3.5–5 μm thick
30
Thallus effuse, granular-dispersed or lacking
31
Thallus continuous or areolate, not granular-dispersed
34
31
Apothecia orange
32
Apothecia golden-yellow, Candelariella- like
32
Ascospores 10–15 μm long
33
Ascospores 15–18.2 μm long
33
Ascospores broadly ellipsoidal to ovoid, (10–)11.5–13 × (5–)6–8.5 μm; septum 5–7 μm thick
Ascospores broadly ellipsoidal to ovoid, 11.5–15 × 8–10 μm; septum 5–6 μm thick
34
On coastal rocks
35
On inland, often alpine to high-alpine rocks
37
35
Thallus bright-yellow or yellow-orange
36
Thallus apricot-orange
36
Thallus bright-yellow; apothecia central, large, 0.5–1.4 mm diam., thalline margin prominent forming a distinctive collar; ascospores broadly ellipsoidal, 13–15(–18) × 5–8 μm, septum (3–)5(–6) μm thick
Thallus golden-yellow to mustard-yellow; apothecia scattered to clustered, 0.1–0.6 mm diam., thalline margin not apparent; ascospores oblong-ellipsoidal, (12–)14–16(–17) × (5–)6.5–7.5(–8.3) μm, septum 3.5–5 μm thick
37
Apothecia red or rusty red-brown
38
Apothecia orange
39
38
Apothecia red, 0.2–0.4 mm diam., angular, 1–6(–15) per areola; thallus greyish brownish; ascospores 9–11 × 5–6 μm, septum 3–3.5 μm thick
Apothecia dark rusty red-brown, 0.5–1.5 mm diam.; thallus whitish or grey-white with scattered orange-red-patches; ascospores ellipsoidal, 11.5–15(–18.5) × 5–7 μm, septum 3.5–5 μm thick
39
Thallus orange-red, continuous, abruptly delimited at margins; apothecia immersed at first becoming sessile, disc orange; ascospores oblong-ellipsoidal, 8–10(–12) × 3.5–(–6.5) μm and a septum ⅓ the length of the spore
Thallus orange, areolate, on a blackish prothallus; apothecia sessile, disc brownish orange; ascospores broadly ellipsoidal, 10–16 × 6–8 μm, septum ⅓ to ½ length of spore
40
Thallus pale- to dark-grey or blackened; alpine
41
Thallus white, creamish or yellow-white; lowland and/or coastal
42
41
Thallus grey-white, not apparent; apothecia clustered, 0.1–0.5(–0.8) mm diam., disc rust-red to dark red-brown; ascospores broadly ellipsoidal to oblong-ellipsoidal, 11.5–13.5(–15) × 6.5–8.5 μm; septum 3.5–5 μm thick
Thallus blue-grey to dark-grey or blackish; apothecia scattered, 0.4–0.8 mm diam., disc grey-black to dark-rust-red; ascospores broadly ellipsoidal 12–17 × 6–9 μm; septum 4–6(–7) μm thick
42
On coastal rocks
43
On lowland, riverine rocks; apothecia waxy, orange-yellow; ascospores ovoid-ellipsoidal, (10–)11.5–13(–15) × 6.5–8.5 μm, septum 5 μm thick
43
Thallus verrucose-papillate, pale greenish white, maculate; apothecial discs orange, with maculate, verrucose-papillate thalline margins; ascospores ellipsoidal, apices rounded, (10–)11.5–13.5 × 5–6.5 μm; septum 2–3.2 μm thick
Thallus thin, areolate, creamish or fawnish, without maculae; apothecial discs golden-yellow, thalline margin granular, not apparent; ascospores narrowly ellipsoidal, apices rounded or slightly pointed at one end, 10–12(–15) × 5–6.5 μm; septum very thin, 1.5–2 μm thick

Caloplaca, included in the family Teloschistaceae (Eriksson et al. 2004; Pennycook & Galloway 2004; Eriksson 2005) is a widespread, cosmopolitan genus of c. 800–1000 species (Kärnefelt et al. 2002; Khodosovtsev et al. 2002; Kärnefelt & Kondratyuk 2004), with taxa known from marine rocks at sea level to high-alpine rocks in all parts of the world including polar regions. In New Zealand, species occur widely on rock (both siliceous rocks and especially also on limestone or calcareous sandstone), living bark, decorticated wood, silty soil, clay and on high-alpine mosses (where they are parasitic), occupying habitats from sea level to 3000 m. It is well developed on rocky shores in all parts of the country, forming part of a distinctive "orange zone", and it is also usually a common component of limestone or other calcareous rocks, again often imparting an orange or yellow-orange tinge to these substrata. At least two species are found parasitic on species of the moss Andreaea in fellfield and high-alpine rock outcrops, and there is a distinctive group of bipolar species found in high-alpine habitats. Although widely distributed and easily recognised, Caloplaca is still very much in need of serious study in New Zealand. A preliminary, "herbarium" account (Galloway 1985a: 60–70), discussed 21 species, but recent collecting and observation of the genus in the field shows that Caloplaca is much more complex here than formerly thought, and that the nature of the substratum may be of considerable importance in assigning species names as suggested by several recent Northern Hemisphere studies (see below).

Several classical accounts of the genus are fundamental to a study of New Zealand populations and include Magnusson (1944a, 1944b, 1950), Poelt (1954, 1965), Wade (1965) and Nordin (1972). Johan Santesson's account of chemistry in Caloplaca (Santesson 1970) is still an extremely useful paper [see also Steiner & Hauschild (1970) and Søchting (1996, 1997)], and the account of species with plurilocular ascospores (Hafellner & Poelt 1979) has information on C. homologa from New Zealand. Recent years have seen considerable interest in Northern Hemisphere and polar populations of Caloplaca, with important contributions coming from five separate schools: (1) the late Josef Poelt and co-workers in Graz (Poelt & Pelleter 1984; Poelt 1985; Poelt & Hinteregger 1993); (2) Ingvar Kärnefelt's school in Lund (Kärnefelt 1988a, 1988b, 1989, 1990a, 1990b, 1991, 1998, 2001, 2003; Arup 1992, 1993, 1994, 1995a, 1995b, 2006; Arup & Mayrhofer 2000; Kärnefelt & Kondratyuk 2004); (3) Ulrich Søchting's school in Copenhagen (Søchting 1973, 1989; Hansen et al. 1987a; Søchting 1992a, 1992b, 1994, 1996, 1997, 1999, 2001; Søchting et al. 1992, 2004;Søchting & Øvstedal 1992, 1998; Søchting & Olech 1995, 2000; Søchting & Lutzoni 2000, 2003; Søchting & Fröberg 2003); (4) Cliff Wetmore's North American school (Wetmore 1994, 1996, 2001, 2003, 2004a, 2004b; Wetmore & Kärnefelt 1998, 1999); and (5) the Spanish school (Navarro-Rosinés & Hladun 1996; Navarro-Rosinés et al. 2000a, 2000b, 2001). Other accounts and/or keys of the genus include: Nimis (1992), Van den Boom et al. (1998), Øvstedal and Lewis Smith (2001) and Kondratyuk et al. (2003). The atlas of British species of Caloplaca (Coppins & Fletcher 2001a–f) also contains much pertinent information. Currently, there is no world checklist or revision of the entire genus apart from the list of names produced by Cliff Wetmore [http://www.tc.umn.edu/~wetmore/AllCalop.htm]. Gaya et al. (2003) recently investigated the relationships between Caloplaca, Fulgensia and Xanthoria, using ITS sequences, and showed that all three genera are non-monophyletic. Søchting et al. (2004) accept the genus Huea C.W.Dodge & G.E.Baker some Antarctic species of Caloplaca with lecideine apothecia.

Although the present account discusses 43 species, it remains a rapid and provisional study and is not a thorough revision. Regional collecting still needs to be undertaken, especially from coastal rocks, from calcareous substrata, from living bark and dead wood, and from high-alpine habitats, before Caloplaca can be assumed to be well understood here.

Species of Caloplaca are often parasitised by lichenicolous fungi, with the following genera being known from Caloplaca in New Zealand: * Arthonia molendoi (q.v.); * Lichenodiplis lecanorae (q.v.); * Muellerella lichenicola (q.v.) and * Polycoccum rugulosarium (q.v.). A diligent search should be made for additional taxa.

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