The phylogeny of the Micarea prasina group was investigated using mitochondrial small subunit ribosomal DNA sequences from 14 taxa representing this group, four other members of the genus Micarea, and Psilolechia lucida as an outgroup. A total of 31 new mtSSU rDNA sequences were generated, including 10 from the M. micrococca complex. Bayesian, maximum parsimony (MP) and maximum likelihood (ML) methods were used to analyse the data. The results show that M. micrococca is not monophyletic and forms three strongly supported lineages: 1) M. micrococca s. str., 2) M. byssacea (Th. Fr.) Czarnota, Guzow-Krzemiń ska & Coppins comb. nov., and 3) a putative taxon that requires further studies. Micarea viridileprosa is a sister species to M. micrococca s. str. and the recently described M. nowakii is a sister species to M. prasina s. str. The placement of M. tomentosa within the M. prasina group is confirmed. Micarea hedlundii appears to be more closely related to the M. micrococca complex than M. prasina s. str. Descriptions, illustrations, taxonomic remarks, distribution and habitat data for M. micrococca s. str. and M. byssacea are provided. A lectotype for Biatora byssacea Hampe non Zwackh and a neotype for Catillaria prasina [var.] byssacea are selected. The Lichenologist 42(1): 7-21 (

Micarea soralifera sp. nov., a new sorediate species belonging to the M. prasina group, is characterized by soralia developing directly from the endoxylic thallus or small external areoles, as well as the presence of micareic acid. Phylogenetic analyses of mtSSU rDNA sequences have shown that its closest relative is M. subviridescens. ITS rDNA sequence, a marker proposed as the universal barcoding region of fungi, was generated from the holotype.

Bacidina mendax, described here as a new lichen species, appears to be common and widespread, at least in Central Europe. Analyses of the ITS rDNA region and the morphology of specimens showed an intraspecific variation in the new taxon. It differs from B. neosquamulosa in the lack of a subsquamulose thallus, and from B. caligans in its longer and only slightly curved to apically hooked conidia and lack of a granular (sorediate) thallus. Since ITS rDNA data support the inclusion of Bacidia pycnidiata Czarnota & Coppins in the genus Bacidina, a new combination is proposed.

We tested two methods to obtain more complete species inventories in surveys of lichen biodiversity. Th e fi rst was to employ eight lichenologists (all experienced, some specialists) acting as individuals in parallel in a competitive survey. Th e second was to organize those lichenologists into two competing teams. We show that overall recorded biodiversity is distinctly higher than the part of lichen biodiversity recorded by each single lichenologist (45 -66%) or team (79 -83%). Use of these methods in a survey of epiphytic and epixylic lichens resulted in a list containing 112 species in 1 ha, 192 species in 12.5 ha and 212 species for 30 km 2 of lowland fl oodplain old-growth forest in southeastern Czech Republic. Eleven recorded species are new to the country; four are rediscovered after more than 50 years. In comparison, few previous surveys of mixed montane forests in the same region have yielded more than 200 species, even though it is certain that those forests have greater lichen diversity than our lowland forest.

Summary The growth rate inhibition of dermatophytes by compounds extracted by acetone, ethanol, methanol and water derived from representatives of several lichen genera (e.g. Caloplaca, Everniastrum, Heterodermia, Hypotrachyna, Platismatia and Ramalina) were compared on the basis of a worldwide review of published research. The examined dermatophytes included Epidermophyton floccosum, Microsporum audouinii, M. canis, M. gypseum, M. nanum, Trichophyton longifusus, T. mentagrophytes, T. rubrum, T. tonsurans and T. violaceum. The influence of selected secondary lichen compounds, for example, usnic acid, on the growth rates of these dermatophytes was also reviewed. The measurement of inhibition by lichen compounds was performed by several methods, but mostly those employing disc diffusion, broth dilution and agar dilution. The fungicidal activity of water‐extracted compounds from Heterodermia leucomela and Hypotrachyna cirrhata and of methanol‐extracted compounds from Evernia divaricata and Ramalina pollinaria, as well as protolichesterinic and 2‐hydroxy‐4‐methoxy‐3,6‐dimethylbenzoic acids, are distinguished.