Peltigera globulata Miadl. & Magain, a new species in the P. ponojensis/monticola species complex of section Peltigera, is formally described. This clade was previously given the interim designation Peltigera sp. 17. It is found in sun-exposed and xeric habitats at high altitudes in Peru and Ecuador. Peltigera globulata can be easily recognized by its irregularly globulated margins covered mostly by thick, white pruina, somewhat resembling the sorediate thallus margins of P. soredians, another South American species from section Peltigera. The hypervariable region of ITS1 (ITS1-HR), which is in general highly variable among species of section Peltigera, does not have diagnostic value for species identification within the P. ponojensis/monticola complex. Nevertheless, no significant level of gene flow was detected among eight lineages representing a clade of putative species (including P. globulata) within this complex. ITS sequences from the holotype specimens of P. monticola Vitik. (collected in 1979) and P. soredians Vitik. (collected in 1981) and lectotype specimens of P. antarctica C. W. Dodge (collected in 1941) and P. aubertii C. W. Dodge (collected in 1952) were successfully obtained through Sanger and Illumina metagenomic sequencing. BLAST results of these sequences revealed that the type specimen of P. monticola falls within the P. monticola/ponojensis 7 clade, which represents P. monticola s. str., and confirmed that the type specimen of P. aubertii falls within a clade identified previously as P. aubertii based on morphology. The ITS sequence from the type specimen of P. soredians, which superficially resembles P. globulata, confirms its placement in the P. rufescens clade. Finally, we discovered that the name P. antarctica was erroneously applied to a lineage in the P. ponojensis/monticola clade. The ITS sequence from the type specimen of P. antarctica represents a lineage within the P. rufescens clade, which is sister to the P. ponojensis/monticola clade.

Tropical mountain forests are hotspots of biodiversity that are widely threatened by human population pressure and climate change. However, the cryptogamic species richness of many tropical mountain regions is insufficiently known, the poorly understood biodiversity of tropical African lichens being a prime example. To study the diversity of the genus Peltigera (Ascomycota, Lecanoromycetes) in East Africa, we studied lichens in a wide range of habitats on the slopes of Mt Kilimanjaro in Tanzania. Ranging from savannah to alpine heath vegetation and from natural forests to agricultural environments, 13 habitat types were sampled for lichens, which were then identified based on the nuITS genetic marker and morphology. We found eight Peltigera species on the slopes of Mt Kilimanjaro, including P. alkalicola sp. nov., P. dolichorhiza, P. polydactyloides, P. praetextata, P. rufescentiformis, P. seneca, P. sorediifera and P. ulcerata. Peltigera is most common and species-rich in the subalpine Erica forest zone, and four of the eight detected species were present only in the subalpine and alpine vegetation zones. Peltigera alkalicola was identified as a previously undescribed species, growing on trachybasaltic lava in the subalpine and alpine zones of Mt Kilimanjaro. The species resembles P. lepidophora but differs by possessing smaller thalli and peltate isidia that are distinctly dark on the lighter, tomentose lamina. Based on data from the NCBI GenBank, P. alkalicola probably also occurs in Alaska (USA) and Ningxia (China). This suggests that even though the species might generally be rare, it may have a global distribution in extreme mountain environments. For the first time, we report P. sorediifera from Tanzania and P. seneca from Africa.

The Rostania occultata species complex (‘Collema occultatum s. lat.’) is revised in Fennoscandia and found to consist of four species, all epiphytes on deciduous trees: Rostania effusa A. Košuth., M. Westb. & Wedin sp. nov., R. occultata (Bagl.) Otálora et al., R. pallida A. Košuth., M. Westb. & Wedin sp. nov. and R. populina (Th. Fr.) A. Košuth., M. Westb. & Wedin comb. nov. Rostania effusa and R. pallida are newly described from humid habitats in old-growth boreal coniferous forests, usually with a mixture of deciduous trees, and from similar areas in the subalpine birch-dominated forests of Fennoscandia. Rostania effusa is characterized by apothecia with red-brown apothecium discs and an excipulum thallinum with a simple pseudocortex and cubic to oblong, muriform spores. Rostania pallida has apothecia with whitish to pale yellowish discs and an excipulum thallinum with a distinct cellular pseudocortex, and ellipsoid, muriform mature spores that are often constricted at the centre. A lectotype is designated for Collema quadratum J. Lahm ex Körb. The new combination Rostania populina is introduced for the species recognized until now as the variety Rostania occultata var. populina (Th. Fr.) Perlmutter & Rivas Plata. A key to the six species in Rostania s. str. is included.

A revision of the North American members of the Leptogium saturninum group (i.e. species with long lower-surface hairs, isidia, and usually smooth upper surface) is presented based on molecular phylogenetic analyses of mtSSU and nrITS sequence data, together with an extensive morphological study. Three species supported by both molecular and morphological characteristics are recognized: L. acadiense sp. nov. (distinguished by granular saturninum-type isidia, medulla composed of irregularly arranged or perpendicular hyphae), L. cookii sp. nov. (distinguished by cylindrical saturninum-type isidia) and L. hirsutum (distinguished by hirsutum-type isidia and medulla composed of loosely intertwined hyphae). One species supported by morphological characteristics, but for which no molecular data could be generated, is also recognized: L. compactum sp. nov. (distinguished by hirsutum-type isidia and medulla composed of tightly packed hyphae). Finally, L. saturninum (distinguished by granular saturninum-type isidia and medulla composed of perpendicular and parallel hyphae) is supported by morphological characteristics but molecular data from geographically diverse populations, including those near the type locality, indicate that the morphologically defined species is paraphyletic. Leptogium burnetiae is excluded from North American based on morphological study of the type. The species are described and illustrated in detail, and are distinguished morphologically by their isidium development, morphology of mature isidia, and pattern of hyphae in the medulla in transverse sections near lobe margins. A key to the members of the L. saturninum group and related species is also presented.

The composition of fatty acids (FAs) is known to discriminate families within genera of bacteria, fungi, octocorals and algae. Here, we applied the more sensitive gas chromatographic (GC) analysis to investigate the taxonomic value of using FA composition to discriminate 15 species of lichen, including three chlorolichens (two Cladonia species and Stereocaulon scutelligerum), nine tripartite lichens (Stereocaulon species) and three cyanolichens (Lichina pygmaea, Collema cristatum, Peltigera membranacea). One macroscopic cyanobacterium (Nostoc sp.), corresponding to the photobiont partner of Peltigera and Collema cyanolichens, was included for comparison. Five lipid extraction methods were evaluated, using Stereocaulon scutelligerum. Shaking at 80 °C with chloroform/methanol (2:1, v/v) was the most efficient and reproducible method. The total FA composition of the 16 species was compared, using GC coupled with flame ionization detection or mass spectrometry. A statistical hierarchical cluster analysis was used to determine the similarity between the FA profiles, based on total, saturated, unsaturated and branched-chain FAs (BCFAs). The BCFA profile allowed a distinction between the Stereocaulon species and the cyanolichens, in contrast to all the other types of FAs. A detailed characterization of eight FA subclasses, provided by the GC analysis, suggested a preferential pathway for the biogenesis of unsaturated FAs through desaturases, which was especially favoured in the cyanolichens.

The cyanolichen genus Epiphloea is currently included within the Heppiaceae (Lichinomycetes) based on ascus characteristics. The presumed presence of a prototunicate ascus has been used as support for this classification, despite the incongruence with other characters (e.g. spores). Here, we use a molecular phylogeny of the two markers mtSSU rDNA and Mcm7 to investigate the position of Epiphloea. In addition, we have re-investigated the ascus characteristics. Our results place the two species, Epiphloea byssina and E. terrena, within the Collemataceae, nested in Leptogium s. str. The ascus type in both species is shown to be Lecanoralean and similar to the ascus in other Collemataceae, with a strongly amyloid tube-like structure. This observation supports the placement within Lecanoromycetes and refutes the earlier suggested affinities with Heppiaceae and Lichinomycetes. The correct names for these species are Leptogium byssinum and Leptogium terrenum.

Molecular inferences of three loci within a phylogenetic framework of a subset of the Pannariaceae confirm that the genus Kroswia is nested within the genus Fuscopannaria. The formal combination of the type species of Kroswia into Fuscopannaria is therefore made here, and Kroswia is reduced into synonymy with the latter genus.

The phylogenetic placement of Collema fasciculare (L.) F. H. Wigg, the most deviating species within Collema (Collemataceae, Lecanoromycetidae), was studied using maximum likelihood and Bayesian analysis of three molecular loci (mitochondrial SSU rDNA, and the protein-coding, nuclear RPB1 and MCM7 genes). Collema fasciculare belongs to Arctomiaceae (Ostropomycetidae) forming a strongly supported monophyletic group with members of Arctomia. The spores, paraphyses, asci and hymenial reactions in Collema fasciculare are similar to other Arctomia, but the ascoma ontogeny is somewhat different. Also C. leptosporum Malme, another species in the Fasciculare group, shows similarities with Arctomia regarding spores and asci. Arctomia is morphologically heterogeneous and the genus is in need of revision. Until then, the species of the Fasciculare group fit best in Arctomia s. lat. and the combinations Arctomia fascicularis (L.) Otálora & Wedin, Arctomia leptospora (Malme) Otálora & Wedin, Arctomia papuanarum (Degel.) Otálora & Wedin and Arctomia uviformis (Hue) Otálora & Wedin are proposed.

Canopy lichen abundance was assessed by size class on regenerating hemlocks, comparing trees of similar size and age (c. 120–140 yrs) growing in the understorey of old-growth cedar-hemlock stands with those growing in adjacent even-aged hemlock stands (natural origin patches c. 1–3 ha in size). Five chlorolichen taxa were associated with old-growth understorey trees: Cavernularia hultenii, Hypogymnia vitatta, Parmelia hygrophila, Platismatia norvegica, and Usnea spp. Lobaria pulmonaria was the most abundant cyanolichen on regenerating hemlock in the old-growth forest stands, particularly in lower canopy (under 12 m) exposures. However, other cyanolichen taxa such as Nephroma helveticum, Sticta fulginosa, and Pseudocyphellaria anomala, reached their greatest abundance at mid-canopy (12–24 m) positions. Smaller cyanolichen thalli (<9 cm2) were abundant on regenerating hemlocks across all canopy positions in the old-growth forest, raising the question as to whether or not cyanolichen thalli in mid- to upper-canopy environments represented long-established individuals facing severe growth constraints, or were simply thalli that had experienced higher rates of fragmentation, and thus did not achieve larger sizes. In comparison, cyanolichens of all taxa were essentially absent from the small-patch even-aged forest stands. Given that dispersal of propagules was not likely a major limiting factor, these 120–140 year old even-age stands may not yet have attained sufficient old-growth characteristics (especially canopy microclimate and canopy throughflow enrichment) to support cyanolichen growth. These findings have major conservation biology implications for wet interior cedar-hemlock forests in British Columbia, where forest harvesting is creating a mosaic of even-aged stands, whose projected age at the time of next harvest (rotation age) will be 120 years or less.