Argüello et al. (2007) found that Parmelina quercina, as circumscribed by Hale (1976), comprised four phylogenetic species which could also be distinguished by morphological features and also had different distributions: P. carporrhizans (usually rhizinate apothecia, and distinct effigurate maculae; oceanic Europe and Macaronesia), P. coleae (usually rhizinate apothecia, narrow ascospores, and fenestrate maculae; North America), P. elixia (non-rhizinate apothecia, larger ascospores, smaller conidia, and not or faintly maculate; Australia), and P. quercina (apothecia rhizinate or not, and less distinct more rounded maculae; continental Europe).

The new species Parmeliella borbonica is described. It belongs in a small group of species, which, unlike all other Parmeliella species except those of the Parmeliella mariana group, have thalline squamulose margins of the apothecia, and are thus superficially reminiscent of Pannaria. The group is mainly Indo-pacific. A key to the species is given. Parmeliella borbonica appears to be an addition to the many remarkable endemic members of the Pannariaceae found in Réunion which has retained old Gondwana elements, as its lowland forests have not been destroyed as much as those in the neighbouring region. The very rare Coccocarpia imbricascens Nyl. was found as new to the island, and the rare endemic Pannaria multifida P. M. Jørg close to its type locality.

Eleven new species of crustose, lichenized fungi are described from the Falkland Islands (Islas Malvinas). Nine species are saxicolous, whereas Lecania vermispora occurs on the stems of Hebe elliptica and Tephromela lignicola is lignicolous on fence posts. The new species are: Bacidia marina, with a sordid blue-green K−, N+ violet epihymenium and acicular, multiseptate ascospores; B. pruinata, with pruinose apothecia and multiseptate ascospores; Buellia gypsyensis, with a thallus containing 5-O-methylhiascic acid and with Amandinea-type conidia; Cliostomum albidum, with pruinose apothecia lacking pigments; C. longisporum, with long narrow ascospores (c. 20 × 3 µm); Coccotrema rubromarginatum, with a placodioid thallus having a red-brown margin and lower surface; Hymenelia microcarpa, with minute, immersed apothecia (<0·1 mm diam.) and a trebouxioid photobiont; Lecania vermispora, with vermiform, 3–6 septate ascospores; Lepra argentea, with papillate isidia with dark caps; Rhizocarpon malvinae, which is similar to R. reductum but with a grey thallus, generally sessile apothecia with a thick raised margin and often with the Cinereorufa-green pigment in the epithecium and upper exciple; and Tephromela lignicola, a sterile, sorediate species on fence posts. Most of these species are reported only from the Falkland Islands although Coccotrema rubromarginatum is also reported from Isla de los Estados and Isla Grande de Tierra del Fuego, Argentina. Ascoconidia are reported from Lepra argentea and cephalodia from Pertusaria pachythallina. Keys to the species reported from the Falkland Islands in the genera of the newly described species are also provided.

Previous studies have identified a close relationship between the monospecific Masonhalea richardsonii and Tuckermannopsis inermis. However, formal taxonomic changes were postponed until existing sequence data could be confirmed. Here we validate these data and discuss the transfer of T. inermis to Masonhalea (made by Lumbsch et al. in Thell & Moberg 2011), consider the morphological, anatomical and biogeographic similarities and differences between these two taxa. The two Masonhalea species both produce lateral apothecia, marginal pycnidia, a layer of cortical tissue beneath the pycnidial wall and bacillariform conidia.

The new species, Solenopsora tasmanica Kantvilas, is described and its distinguishing characteristics are discussed. The new species is the first record for the genus for Tasmania and occurs on montane, acidic soils, an unusual habitat for Solenopsora. It also contains the compounds brialmontin 1 and brialmontin 2, recorded from Solenopsora for the first time.

A set of artificial keys is presented to all those crustose lichens (except most species of Lepraria and Leprolomd) which commonly occur without fruiting bodies on rock or soil in the British Isles. A number of predominantly corticolous species that occasionally also occur on rocks are included, as well as several undescribed but well-understood entities.

Growth of the mycobiont of Ramalina siliquosa and the secondary metabolites subsequently produced under various osmotic culture conditions were examined. The secondary metabolite content and the growth rate changed greatly when different quantities of sucrose were added to the culture medium. Salazinic acid was found only in mycobionts cultured on a medium with 10 or 20% sucrose, the mycobiont growth rate being higher than on conventional medium. Similarly, in Lobaria discolor, gyrophoric acid was found only in mycobionts cultured on a medium with 10% sucrose.

The results of nitrogen (N) analyses of 14 New Zealand and 23 Antarctic lichens are reported. Eight percent of the total lichen N occurs in the form of amino sugars, 5° as nucleic acids and 80° as proteins and amino acids. It is concluded that when lichens decompose they may represent a good N resource that may be important in ecosystems.

A new species of Synarthonia, S. leproidica, is described from Luxembourg. Phylogenetic analyses of mtSSU and RPB2 sequences were used to determine the generic affiliation of this sterile species. Synarthonia leproidica differs from all other species of the genus by the combination of a leproid thallus and the production of psoromic acid. It is the sister species to S. muriformis in our phylogenetic analyses. The discovery of the new species suggests that other strictly sorediate lichen species might have been overlooked in Europe, even in intensely explored countries such as Luxembourg. Phylogenetic analyses further confirm the placement of Reichlingia anombrophila in the genus Reichlingia and of Synarthonia astroidestera in the genus Synarthonia. Arthonia atlantica is transferred to the genus Reichlingia as R. dendritica.

In the mid-1950s, two distinguished Italian researchers, the mycologist Raffaele Ciferri (1895–1965) and the phytosociologist Ruggero Tomaselli (1920–1982), decided that a separate system of naming lichen mycobionts independent of the intact thalli was necessary. In this they were stimulated by the pioneering studies of Thomas (1939) in particular, which showed how different cultured isolated mycobionts appeared from whole lichen thalli. Thomas had already introduced separate names, ending in the suffix “-myces”, and they determined to introduce a comprehensive suite of generic names for lichen mycobionts in a series of papers (Tomaselli & Ciferri 1952; Ciferri & Tomaselli 1953, 1954, 1957). The numbers of generic names coined and validly published with Latin diagnoses were substantial: 15 in 1952, 203 in 1953, and a further nine in 1954. They made proposals to change the provisions of the Code, which then already ruled that names given to lichens were to be regarded as applying to their fungal components, but these were defeated and never adopted; this rule remains in the Code in Art. 13.1 (Greuter et al. 2000).

A new fruticulose species, Polycauliona comandorica, is described from the supralittoral zone of the Commander Islands in the Russian Far East. This growth form is very rare in the family Teloschistaceae where the new species belongs. It is the only fruticulose species of the family that forms vegetative propagules (soredia and blastidia). Polycauliona comandorica is similar to the North American P. thamnodes but differs in having a lighter yellow to grey thallus, longer and thicker branches with a rough surface, soredia and blastidia, and in lacking apothecia. Two fruticulose-lobate pairs of species in Polycauliona are briefly discussed: P. comandorica-P. verruculifera and P. thamnodes-P. brattiae.

Porina rivalis Orange is described as new from rocks in streams in Great Britain. The involucrellum is yellow or orange within, but dark grey to purplish red at the surface; the ascospores are 3-septate, 13·0–18·5×4·0–5·5 μm.