Cryptolechia carneolutea is the type species of the genus Cryptolechia, a rare taxon classified as endangered in the UK, now largely confined to ancient Fraxinus trees. The only tree with abundant growth of the species in one of its strongholds, the Slapton Ley National Nature Reserve in Devon, was blown over in a storm in April 2017, making it possible to collect material for molecular studies and transplant specimens to other Fraxinus trees in the area. The results of the phylogenetic analysis revealed C. carneolutea to be nested within the genus Gyalecta (Gyalectaceae). This further supports a broad circumscription of Gyalecta, after also including species previously placed in Belonia and Pachyphiale as proposed in other recent studies. It might be possible to introduce an alternative genus concept in Gyalectaceae, not schematically based on ascoma type and ascospore number, but presently not enough data are available to proceed with such a novel classification. A review of the taxonomic concept of Cryptolechia demonstrates that this name was used inconsistently in the past, and its possible inclusion in Gyalecta was anticipated by other authors. As the majority of species presently classified in Cryptolechia had been placed in Gyalecta before, only five new combinations are required to provide formal inclusion of all taxa in the latter genus: Gyalecta bicellulata (Kalb) D. Hawksw. & Lücking comb. nov., G. caudata (Kalb) D. Hawksw. & Lücking comb. nov., G. pittieriana (Kalb et al.) D. Hawksw. & Lücking comb. nov., G. saxatilis (Vězda) D. Hawksw. & Lücking comb. nov. and G. stellaris (Müll. Arg.) D. Hawksw. & Lücking comb. nov. We also supersede the previous lectotypification of Parmelia carneolutea Turner with the discovery of the holotype specimen in BM.

Three species, Lobothallia brachyloba Paukov & I. V. Frolov, L. epiadelpha Paukov & A. Nordin and L. zogtii Paukov & Davydov, from arid regions of Eurasia (Russia, Kazakhstan, Kyrgyzstan, China and Mongolia) are described as new to science. Lobothallia brachyloba has flat, firmly attached lobes, immersed apothecia lacking a distinct thalline margin, and contains norstictic acid. Both Lobothallia epiadelpha and L. zogtii contain stictic acid and have a brown thallus and sessile apothecia. Lobothallia epiadelpha initially develops on crustose Circinaria spp, has thick lobes loosely attached to the substratum, and brown apothecial discs with constant thalline margins. Lobothallia zogtii is a free-living species with brownish black to jet black apothecial discs surrounded by a receding thalline margin. Lecanora bogdoënsis is synonymized with Lobothallia praeradiosa and Lobothallia helanensis is synonymized with L. subdiffracta. Three new combinations, Lobothallia hedinii (H. Magn.) Paukov, A. Nordin & Sohrabi, L. lacteola (Oxner) Şenkardeşler, Paukov, Davydov & Sohrabi, and L. subdiffracta (H. Magn.) Paukov, are proposed. Phylogenetic analyses of Lobothallia brachyloba, L. epiadelpha and L. subdiffracta (ITS, mtSSU) are presented, showing their relationships within Lobothallia. The lectotype of the name Aspicilia lacteola Oxner is designated. A key to 18 species of Lobothallia is provided.

Species identification in the tropical lichen genus Phyllopsora is generally challenging and is based on ascospore morphology, vegetative dispersal units, thallus structure and secondary chemistry. As several type specimens are in poor condition and difficult to interpret, it is often unclear how these old names fit with the currently used taxonomy. In the present study, we aim to identify species boundaries in Phyllopsora s. str. supported by an integrative approach using multiple sources of evidence. We investigated a substantial amount of herbarium as well as freshly collected material and generated mtSSU and ITS sequence data from most of the described species, including several types. Species delimitation analyses are applied on the gene trees using mPTP and we construct a species tree of both markers with *BEAST, facilitating discussion of species delimitation and sister-relationships. Comparing morphology, chemistry and molecular data, we found that the mPTP analyses split established species repeatedly. Based on our integrative results, we exclude nine species from the genus, resurrect one (P. melanoglauca Zahlbr.), reduce two into synonymy with other Phyllopsora species and describe five as new to science: Phyllopsora amazonica Kistenich & Timdal (which shares the secondary chemistry (atranorin and terpenoid pattern) with P. halei chemotype 1, but differs, e.g., in having smaller areolae that are attached to a thinner, white prothallus, and in having more persistently marginate and less convex apothecia), Phyllopsora concinna Kistenich & Timdal (which shares the secondary chemistry (atranorin and parvifoliellin) with P. parvifoliella and P. rappiana, but differs from both in forming larger isidia, having a white prothallus, apothecial margin paler than the disc, and longer and broader ascospores), Phyllopsora furfurella Kistenich & Timdal (which is here segregated from P. furfuracea based on having a white prothallus and in containing skyrin in the hypothecium (K+ red)), Phyllopsora isidosa Kistenich & Timdal (which differs from P. byssiseda in forming a more crustose thallus with more delicate isidia, and from P. isidiotyla in forming somewhat coarser, less branched isidia) and Phyllopsora neotinica Kistenich & Timdal (a neotropical species here segregated from the now exclusively paleotropical P. chodatinica, differing in containing an unknown xanthone (not chodatin)). Lectotypes are designated for Biatora pyrrhomelaena Tuck., Lecidea leucophyllina Nyl., L. pertexta Nyl., and P. brachyspora Müll. Arg. In total, we accept 54 species in the genus Phyllopsora.