Lasallia hispanica (Frey) Sancho & A. Crespo is one of three Lasallia species occurring in central-western Europe. It is an orophytic, photophilous Mediterranean endemic which is sympatric with the closely related, widely distributed, highly clonal sister taxon L. pustulata in the supra- and oro-Mediterranean belts. We sequenced the genome of L. hispanica from a multispore isolate. The total genome length is 41·2 Mb, including 8488 gene models. We present the annotation of a variety of genes that are involved in protein secretion, mating processes and secondary metabolism, and we report transposable elements. Additionally, we compared the genome of L. hispanica to the closely related, yet ecologically distant, L. pustulata and found high synteny in gene content and order. The newly assembled and annotated L. hispanica genome represents a useful resource for future investigations into niche differentiation, speciation and microevolution in L. hispanica and other members of the genus.

Myriospora signyensis Purvis, Fdez-Brime, M. Westb. & Wedin is described from Signy Island, South Orkney Islands, Antarctica, where it occurs predominantly on quartz mica schist. This represents the first record of the genus for Antarctica. The distinctive interrupted photobiont arrangement places it within the genus Myriospora (formerly known as the ‘Acarospora’ smaragdula group, or Silobia). The new species is characterized by having large, distinctly elevated, sessile apothecia with a prominent margin and a thallus that is usually lobed at the margins and variously orange-red, rust-coloured or brown-pigmented. Molecular phylogenetic analyses inferred with strong support that M. signyensis is closely related to M. scabrida which is similar in having a lobed, imbricate thallus with large and frequently somewhat raised apothecia, but which differs in never being rusty red, by frequently having a larger number of apothecia per areole/squamule and by having a thick and distinctive thalline epinecral layer. Myriospora signyensis is otherwise most similar to M. dilatata but the thallus of M. dilatata is never imbricate-lobate and the ascomata of M. signyensis have larger and more distinctly raised and sessile apothecia. A worldwide key to the 10 species currently recognized in the genus is presented.

Using an ITS mutation rate as calibration reference, a three-locus timetree was generated for the genus Lobaria and its most important clades. The timetree resolved most clades with strong support and gave an estimate of the diversification time for Lobaria during the early Oligocene. A fossil impression from a 12–24 million-year-old Miocene deposit is hypothesized here to belong to an ancestral Lobaria species. Additionally, the age estimate indicates that the paleoclimate and the closing or opening of the Bering Strait played a major role in shaping the current distribution of most Lobaria species. It is hypothesized that the Bering land bridge acted as a major highway during warm-temperate climate periods, but as a barrier during Arctic climate times.

Some definitions of the term ‘lichen’ have often emphasized the role of the mycobiont as exhabitant in the symbiosis. Mastodia tessellata and Turgidosculum ulvae, both forming lichen-like associations with foliose algae, have traditionally defied that definition. In this study, we delve into the poorly known association of T. ulvae with Blidingia minima. Using four molecular markers (nrLSU, nrSSU, RPB1, mtSSU) we show that T. ulvae is a member of the family Verrucariaceae, closely related to the marine species Verrucaria ditmarsica. The presence of bitunicate asci and single-cell ascospores is confirmed. Our analysis of a fragment of the rbcL marker demonstrates that the photosynthetic partner belongs to B. minima, although relationships within this taxon remain unclear. Transmission electron microscopy allowed us to illustrate how T. ulvae interacts with Blidingia cells, and how haustoria in that species differ from those previously investigated in other marine lichen-forming fungi.

Intrathalline phycobiont diversity was investigated in a rosette-forming lichen, Parmotrema pseudotinctorum, using a combination of Sanger sequencing, 454-pyrosequencing, conventional light and confocal microscopy, and transmission electron microscopy. A total of 39 thalli sampled in five Canary Island populations were investigated. Three novel lineages of lichen phycobionts were detected, all being inferred within the Trebouxia clade G. The most abundant phycobiont lineage, occurring in all lichen populations investigated, is described here as Trebouxia crespoana sp. nov. This species produces spherical to pyriform cells possessing a crenulate chloroplast with lobes elongated at their ends, and one corticola-type pyrenoid with very thin, unbranched tubules of curved profile. Trebouxia crespoana is clearly distinguished from all other Trebouxia species by a characteristic cap-like cell wall thickening produced on one side of vegetative cells, and the larger size of vegetative cells that reach 21(–26) µm in diameter.

Lichen thalli represent the most conspicuous examples of fungal-algal interactions. Studies that describe phycobiont diversity within entire thalli are based mainly on Sanger sequencing. In some lichen species, this technique could underestimate the intrathalline coexistence of multiple microalgae. In this study different multi-tool approaches were applied to two lichen taxa, Circinaria hispida and Flavoparmelia soredians, to detect algal coexistence. Here, we combined Sanger sequencing, a specific polymerase chain reaction (PCR) primer, 454-pyrosequencing, phycobiont isolation and ultrastructural characterization. Furthermore, we compared pyrenoid ultrastructural features of lichenized phycobionts with microalgae isolated in culture. An improved methodology was used to isolate and propagate phycobionts which, in combination with fast genetic identification, resulted in a considerable reduction in time and cost to complete the process. This isolation method, coupled with a specific PCR primer, allowed for the detection of coexisting algae in C. hispida (four Trebouxia lineages). 454-pyrosequencing detected only a fraction of such diversity, while Sanger sequencing identified only the primary phycobiont. Ultrastructural features of the isolated algae were observed by transmission electron microscopy; the maintenance of the pyrenoid characteristics suggested the existence of different Trebouxia lineages. In F. soredians a single Trebouxia lineage was identified using all these approaches.

In cases of lichens with algal coexistence, a combination of different molecular and ultrastructural approaches may be required to reveal the underlying algal diversity within a single thallus. The approach proposed in this study provides information about the relationship between molecular and ultrastructural data, and represents an improvement in the delimitation of taxonomic features which is needed to recognize intrathalline Trebouxia diversity.

Chlorophyll a fluorescence is often used to estimate various types of damage in lichens. In order to optimize the output and improve interpretations of such measurements the protocol for pretreatment and measuring is important. To study the effects of measurement conditions, the lichens Lobaria pulmonaria, L. scrobiculata, Xanthoria parietina and Parmelia sulcata were first stressed by high light intensities at 600 or 1000 µmol photons m−2 s−1 for 4 h. Then various conditions during recovery or pretreatment were used to optimize the detection of more lasting damage. Recovery from photoinhibition was incomplete in darkness, whereas light as low as 0·2 or 1·0 µmol m−2 s−1 resulted in complete recovery if the recovery period was long enough. Additionally, low intensity light given for1·5 h after one day in darkness caused rapid and complete recovery. In conclusion, before measuring maximal PSII efficiency (Fv/Fm) with chlorophyll fluorescence, it is important to let lichens recover in low intensity light and not in darkness, to optimize recovery from photoinhibition; dark adaptation can only be recommended if the photoinhibition status of the lichens is of interest.

Currently, change in lichen community structure depends on a combination of several pollutants instead of just one. Consequently, alpha lichen diversity no longer represents an effective response variable for assessing trends in atmospheric pollutants over time. Here we investigated the value of the relationship between alpha diversity and different aspects of gamma diversity (similarity, replacement and differences in richness of species) together with that of beta diversity (calculated as the sum of replacement and difference in richness of species), for assessing complex variations in epiphytic lichen communities in response to a changing pollution scenario. We considered an area subjected to extreme variation in atmospheric pollution in recent decades and explored temporal and spatial aspects of lichen community succession over short-, intermediate- and long-term reference periods. We found that variation in lichen communities for long- and intermediate-term reference periods was strongly dependent on the alpha diversity of single trees at the beginning of the observation period. The occurrence of nitrophytic species, which responded to the decrease in SO2 concentrations, contribute to this trend. The effect of land use was observed only over long observation periods, with trees in urban areas showing less variation than those located in rural areas. In particular, the analysis of similarity, species replacement and differences in richness of tree pairs demonstrated that trends and patterns within lichen communities are neither always nor to the same extent associated with alpha diversity. Our results show that a thorough study of gamma diversity, including beta diversity and similarity, is required to detect changes in air quality in long-term biomonitoring surveys.

This paper, based on data from the latest checklist of Italy, analyzes the distribution patterns of rare and common lichen species within biogeographically homogeneous versus heterogeneous areas of Italy, and the relationships with some main drivers of rarity and commonness. The following data were used: 1) commonness-rarity values of 2565 species in nine ecoregions; 2) frequency of 353 nationally rare and 387 nationally common species in 21 administrative regions. The following functional and ecological traits were considered: growth form, photobiont(s), type of reproduction, substrata, bioclimatic range, ecological indicator values for aridity and eutrophication, and poleophoby. Within each ecoregion, rare species by far outweigh common species but about one third of these are common in other ecoregions. At the level of regional floras, rarity is significantly associated with epiphytic substrata, non-trebouxioid photobionts and high air humidity, while commonness is associated with saxicolous substrata, trebouxioid photobionts and eutrophication. Rarity seems to mainly depend on two factors, bioclimate (many rare species are outside the limit of their bioclimatic optima) and reduced availability of suitable habitats (e.g. old-growth forests), while commonness is mainly related to disturbance (eutrophication, creation of drier habitats). Most of the nationally rare lichens belong to an oceanic-suboceanic element with tropical affinities or to a small set of continental species with their optima in the dry steppe biome, which suggests that many rare species can persist in microrefugia, that is sites with microclimates that support small populations of species beyond the boundaries of the climatic limits of their main distributions.