Taxonomy of Verrucaria species characterised by large spores, perithecia leaving pits in the rock and a pale thin thallus in Finland

Correction: 10.3897/mycokeys.80.67870.Species of Verrucaria, characterised by large spores (at least some spores exceeding 25 mu m in length), perithecia leaving pits in the rock and a pale thin thallus, form a taxonomically-difficult and poorlyknown group. In this study, such species occurring in Finland are revised, based on ITS sequences and morphology. Maximum likelihood analysis of ITS sequence data was used to examine if the species belong to the Thelidium group, as suggested by BLAST search. Twelve species are accepted in Finland: Verrucaria bifurcata sp. nov., V. cavernarum sp. nov., V. devergens, V. difficilis sp. nov., V. foveolata, V. fuscozonata sp. nov., V. karelica, V. kuusamoensis sp. nov., V. subdevergens sp. nov., V. subjunctiva, V. subtilis and V. vacillans sp. nov. Verrucaria foveolata is nested in V. subjunctiva in the phylogeny, but due to morphological and ecogeographical differences, the two taxa are treated as separate species pending further studies. Based on the analysis, the study species belong to the Thelidium group. The studied species show a rather high infraspecific morphological, but a low genetic variation. Furthermore, they show considerable overlap in their morphology and many specimens cannot be reliably identified, based on morphology only. All species arc restricted to calcareous rocks. Verrucaria alpigena, V. cinereoruh and V. bochstetteri are excluded from the lichen flora of Finland. Verrucaria gmssa is considered a species with unresolved identity. Verrucaria foveolata and V. subtilis are rather common on calcareous rocks of Finland while V. devergens and V. kuusamoensis are restricted to northern Finland. Verrucaria subjunctiva occurs mainly in northern Finland. Verrucaria bifurcata has been found only from southern Finland. Verrucaria difficilis has few localities both in SW and NE Finland. Verrucaria vaeillans is restricted to calcareous roc ks (dolomite) on the mountains of the NW corner of Finland. Verrucaria Jiacozonata, V. karelica and V. sulideveTens occur only in the Oulanka area in NE Finland. A lectotype is designated for V. subjunctiva. The morphology of the Finnish species was compared with 51 European species of Verrucaria presumably belonging to the Theliolium group.Peer reviewe

Arthonia ligniariella new to Finland

Arthonia ligniariella Coppins is reported for the first time from Finland. The specimen was collected on a dead, standing pine tree in Vesijako strict nature reserve in southern Finland. It is likely an overlooked species in Finland and possibly rare. It should be looked for in old-growth forests on dead wood and bark of various tree species, as well as on moribund mosses.Peer reviewe

Growth form matters-Crustose lichens on dead wood are sensitive to forest management

Lichens have a vital role in forest ecosystems and they are a threatened group in boreal forests. However, the conservation ecology of the total lichen community has very rarely been studied. Here we studied lichen species and communities, including macrolichens (=foliose and fruticose growth forms) and rarely studied crustose li-chens, on decaying wood in boreal spruce-dominated forests in Finland. We also studied obligate lignicoles that grow only on dead wood and are mostly crustose in growth form. Species richness and community composition were examined on decaying logs and natural or cut stumps of Picea abies at different decay stages (2-5) in 14 stands, half of which were natural or seminatural and half recently managed. We used thorough search to yield a species list as close to complete as possible. Our study questions were: 1) Are species richness and lichen communities different in natural and managed forests, and if so, are there differences between macrolichens, crustose lichens and obligate lignicoles in how they respond to forest management? 2) How does the decay stage and dead wood type affect the lichens, i.e. are there differences between stumps and logs? We found a total of 127 lichen species. Most (75 %) of the recorded lichen species were crustose. With a generalized linear model we found that crustose lichens and obligate lignicoles had a higher species richness in natural than managed forests, but macrolichen richness was not significantly affected by forest management. Utilizing non-metric multidi-mensional scaling we discovered that site level community composition of macrolichens, crustose lichens and obligate lignicoles was also significantly different between natural and managed forests. We found that on dead wood unit level the decay stage had a significant effect on species richness and community composition, so that the species richness of all studied groups declined during the decay process. The dead wood type (stump vs log) had a significant effect on species richness of macrolichens and obligate lignicoles, both for which species richness was higher on logs than on stumps, as well as on the communities of crustose lichens.Peer reviewe

Lichen speciation is sparked by a substrate requirement shift and reproduction mode differentiation

Publisher Copyright: © 2022, The Author(s).We show that obligate lignicoles in lichenized Micarea are predominately asexual whereas most facultative lignicoles reproduce sexually. Our phylogenetic analyses (ITS, mtSSU, Mcm7) together with ancestral state reconstruction show that the shift in reproduction mode has evolved independently several times within the group and that facultative and obligate lignicoles are sister species. The analyses support the assumption that the ancestor of these species was a facultative lignicole. We hypothezise that a shift in substrate requirement from bark to wood leads to differentiation in reproduction mode and becomes a driver of speciation. This is the first example of lichenized fungi where reproduction mode is connected to substrate requirement. This is also the first example where such an association is demonstrated to spark lichen speciation. Our main hypothesis is that obligate species on dead wood need to colonize new suitable substrata relatively fast and asexual reproduction is more effective a strategy for successful colonization.Peer reviewe

New Micarea records from Norway and Sweden and an identification key to the M. prasina group in Europe

Micarea czarnotae and M. pseudomicrococca are reported as new to Sweden, and M. fallax is reported as new to Norway. Micarea laeta and M. melanobola are reported from Sweden for the first time since 1927 and 1892, respectively. Micarea fallax is reported from three new localities in Sweden. An updated identification key for the M. prasina group in Central and Northern Europe is provided.Peer reviewe

Seven Micarea (Pilocarpaceae) species new to Germany and notes on deficiently known species in the Bavarian Forest

We report new records of 19, predominantly rare, Micarea species, mostly from dead wood in mixed montane forests characterized mainly by Norway spruce, European beech and silver fir in the Bavarian Forest National Park on the German-Czech border. Their ecology and key morphological features are discussed. Micarea contexta, M. fallax, M. melanobola, M. pseudomicrococca, M. pusilla, M. soralifera and M. tomentosa are reported for the first time from Germany. Micarea anterior, M. byssacea, M. elachista, M. laeta, M. micrococca and M. nowakii, in addition to the aforementioned, are reported as new for the Bavarian Forest National Park.We report new records of 19, predominantly rare, Micarea species, mostly from dead wood in mixed montane forests characterized mainly by Norway spruce, European beech and silver fir in the Bavarian Forest National Park on the German-Czech border. Their ecology and key morphological features are discussed. Micarea contexta, M. fallax. M. melanobola, M. pseudomicrococca, M. pusilla, M. soralifera and M. tomentosa are reported for the first time from Germany. Micarea anterior, M. byssacea, M. elachista, M. laeta, M. rnicrococca and M. nowakii, in addition to the aforementioned, are reported as new for the Bavarian Forest National Park.Peer reviewe

Growth form matters – Crustose lichens on dead wood are sensitive to forest management

Lichens have a vital role in forest ecosystems and they are a threatened group in boreal forests. However, the conservation ecology of the total lichen community has very rarely been studied. Here we studied lichen species and communities, including macrolichens (=foliose and fruticose growth forms) and rarely studied crustose lichens, on decaying wood in boreal spruce-dominated forests in Finland. We also studied obligate lignicoles that grow only on dead wood and are mostly crustose in growth form. Species richness and community composition were examined on decaying logs and natural or cut stumps of Picea abies at different decay stages (2–5) in 14 stands, half of which were natural or seminatural and half recently managed. We used thorough search to yield a species list as close to complete as possible. Our study questions were: 1) Are species richness and lichen communities different in natural and managed forests, and if so, are there differences between macrolichens, crustose lichens and obligate lignicoles in how they respond to forest management? 2) How does the decay stage and dead wood type affect the lichens, i.e. are there differences between stumps and logs? We found a total of 127 lichen species. Most (75 %) of the recorded lichen species were crustose. With a generalized linear model we found that crustose lichens and obligate lignicoles had a higher species richness in natural than managed forests, but macrolichen richness was not significantly affected by forest management. Utilizing non-metric multidimensional scaling we discovered that site level community composition of macrolichens, crustose lichens and obligate lignicoles was also significantly different between natural and managed forests. We found that on dead wood unit level the decay stage had a significant effect on species richness and community composition, so that the species richness of all studied groups declined during the decay process. The dead wood type (stump vs log) had a significant effect on species richness of macrolichens and obligate lignicoles, both for which species richness was higher on logs than on stumps, as well as on the communities of crustose lichens.</p

Four new Micarea species from the montane cloud forests of Taita Hills, Kenya

The genus Micarea was studied for the first time in the Taita Hills, Kenya. Based on new collections and existing data, we reconstructed a phylogeny using ITS, mtSSU and Mcm7 regions, and generated a total of 27 new sequences. Data were analyzed using maximum likelihood and maximum parsimony methods. Based mainly on new collections, we discovered four undescribed well-supported lineages, characterized by molecular and phenotypic features. These lineages are described here as Micarea pumila, M. stellaris, M. taitensis and M. versicolor. Micarea pumila is characterized by a minutely granular thallus, small cream-white or pale brownish apothecia, small ascospores and the production of prasinic acid. Micarea stellaris has a warted-areolate thallus, cream-white apothecia usually darker at the centre, a hymenium of light grey or brownish pigment that dissolves in K, and intense crystalline granules that appear as a belt-like continuum across the lower hymenium when studied in polarized light. Micarea taitensis is characterized by a warted-areolate thallus and cream-white or yellowish apothecia that sometimes produce the Sedifolia-grey pigment. Micarea versicolor is characterized by a warted-areolate, sometimes partly granular thallus and apothecia varying from cream-white to light grey to blackish in colour. This considerable variation in the coloration of its apothecia is caused by an occasional mixture of the Sedifolia-grey pigment in the epihymenium and another purplish brown pigment in the hymenium. Micarea stellaris, M. taitensis and M. versicolor produce methoxymicareic acid. The main distinguishing characters are presented in a species synopsis. Three of the new species are nested in the M. prasina group, and the fourth one (M. taitensis) resolves as a basal taxon to the M. prasina group. The new species inhabit montane cloud forests, which have fragmented dramatically throughout the Eastern Arc Mountains in recent decades.The genus Micarea was studied for the first time in the Taita Hills, Kenya. Based on new collections and existing data, we reconstructed a phylogeny using ITS, mtSSU and Mcm7 regions, and generated a total of 27 new sequences. Data were analyzed using maximum likelihood and maximum parsimony methods. Based mainly on new collections, we discovered four undescribed well-supported lineages, characterized by molecular and phenotypic features. These lineages are described here as Micarea pumila, M. stellaris, M. taitensis and M. versicolor. Micarea pumila is characterized by a minutely granular thallus, small cream-white or pale brownish apothecia, small ascospores and the production of prasinic acid. Micarea stellaris has a warted-areolate thallus, cream-white apothecia usually darker at the centre, a hymenium of light grey or brownish pigment that dissolves in K, and intense crystalline granules that appear as a belt-like continuum across the lower hymenium when studied in polarized light. Micarea taitensis is characterized by a warted-areolate thallus and cream-white or yellowish apothecia that sometimes produce the Sedifolia-grey pigment. Micarea versicolor is characterized by a warted-areolate, sometimes partly granular thallus and apothecia varying from cream-white to light grey to blackish in colour. This considerable variation in the coloration of its apothecia is caused by an occasional mixture of the Sedifolia-grey pigment in the epihymenium and another purplish brown pigment in the hymenium. Micarea stellaris, M. taitensis and M. versicolor produce methoxymicareic acid. The main distinguishing characters are presented in a species synopsis. Three of the new species are nested in the M. prasina group, and the fourth one (M. taitensis) resolves as a basal taxon to the M. prasina group. The new species inhabit montane cloud forests, which have fragmented dramatically throughout the Eastern Arc Mountains in recent decades.Peer reviewe

Taxonomy of Thelidium auruntii and T. incavatum complexes (lichenized Ascomycota, Verrucariales) in Finland

The taxonomy of lichen species morphologically similar to Thelidium auruntii and T. incavatum in Finland is being revised. Based on ITS and morphology, ten species occur in Finland. All species are restricted to calcareous rocks. The Thelidium auruntii morphocomplex includes six species: T. auruntii, T. huuskonenii sp. nov., T. pseudoauruntii sp. nov., T. sallaense sp. nov, T. toskalharjiense sp. nov. and T. sp. 1. In the ITS phylogeny, T. auruntii, T. pseudoauruntii and T. sallaense group together, but the remaining species are placed outside of this clade. All the species have northern distribution in Finland, occurring on fells in NW Finland and/or in gorges in the Oulanka area in NE Finland. The Thelidium incavatum morphocomplex includes four species: T. declivum sp. nov., T. incavatum, T. mendax sp. nov. and T. sp. 2. This morphogroup is not resolved as monophyletic in the ITS phylogeny, with only T. declivum and T. mendax forming a strongly supported group. Thelidium incavatum is rather common in SW Finland, with one separate locality in eastern Finland. Thelidium declivum occurs only in the Oulanka area. Thelidium mendax occurs in the Oulanka area, but one locality is known from eastern central Finland. Thelidium sp. 2 is known from one locality in SW Lapland