Abstract
Lepraria juanfernandezii
is described as a new species. It differs from all other species of
Lepraria
by its aggregate thallus with sparse prothallus hyphae, the absence of a hypothallus, ...the presence of divaricatic acid and the absence of zeorin, and its occurrence in the Southern Hemisphere. A key to all species of
Lepraria
containing divaricatic acid is given.
The landscape-scale extinction of a tree species may have a negative impact on diversity of associated epiphytic species. We used ordination and hierarchical clustering methods to assess landscape ...and the community level effects of reduction in the abundance of European ash
Fraxinus excelsior
, caused by ash dieback, on the associated epiphytic lichen biota in Białowieża Forest (Poland)—the best preserved forest complex in Central Europe. At the landscape level ash decline impact on the biota of ash-associated epiphytic lichens was weak, due to the high diversity of tree species, which may serve as potential alternative hosts. At this level, oak and hornbeam are the most important alternative hosts, assuring the maintenance of ash-associated epiphytic lichens. Lime, alder, and hazel appeared to be less important but still may serve as substitute phorophytes to approximately 2/3 of the ash-associated lichen biota. About 90% of epiphytic biota are likely to survive on the landscape scale. However, at the community level of alder-ash floodplain forest, where ash was dominant, about 50% of ash-associated epiphytic lichen species are threatened by ash dieback. Our results highlight the importance of a spatial scale in conservation biology. Protection of large forest areas with rich diversity of phorophyte trees increases chances of survival of the associated epiphytic organisms.
We studied the biodiversity of Asterochloris photobionts found in Bolivian lichens to better understand their global spatial distribution and adaptation strategies in the context of a worldwide ...phylogeny of the genus. Based on nuclear ITS rDNA, the chloroplast rbcL gene and the actin type I gene we reconstructed a phylogenetic tree that recovered nine new Asterochloris lineages, while 32 Bolivian photobiont samples were assigned to 12 previously recognized Asterochloris lineages. We also show that some previously discovered Asterochloris photobiont species and lineages may occur in a broader spectrum of climatic conditions, and mycobiont species and photobionts may show different preferences along an altitude gradient. To reveal general patterns of of mycobiont specificity towards the photobiont in Asterochloris, we tested the influence of climate, altitude, geographical distance and effects of symbiotic partner (mycobiont) at the species level of three genera of lichen forming fungi: Stereocaulon, Cladonia and Lepraria. Further, we compared the specificity of mycobionts towards Asterochloris photobionts in cosmopolitan, Neotropical, and Pantropical lichen forming fungi. Interestingly, cosmopolitan species showed the lowest specificity to their photobionts, but also the lowest haplotype diversity. Neotropical and Paleotropical mycobionts, however, were more specific.
Bryophytes and lichens are outstanding bioindicators, not only of the plant community in which they develop, but also the substrates on which they grow. Some epiphytic cryptogams, particularly the ...rare ones, are stenotopic and require a long habitat continuity, for example substrates such as old trees. It could also be a tea plantation, this is because the shrubs are not felled, and most of them may have several dozen years. In addition, the shrubs are not subject to sudden changes in microclimatic conditions as only the young leaves are harvested. As the importance of tea plantations as host plants for mosses and lichens has not yet been studied, the present study examines the species diversity of cryptogams of two tea plantations in Georgia (Caucasus). The study also examines the phytogeography, spatial pattern, environmental conditions and ecological indicators of the cryptogams. Thirty-nine cryptogam taxa were identified; typical forest taxa dominated, even in the absence of typical forest communities. Some of these species are obligatory epiphytes, rare or even critically endangered in most European countries (e.g., Orthotrichum stellatum, O. stramineum, Lewinskya striata). The fairly abundant record of such species on tea plantations indicates the importance of these phytocoenoses for the preservation of rare species, and indicates that these habitats are hot spots for these cryptogams in otherwise changed envirnonment. Additionally, as indicated the analysis of the species composition of individual plantations and the mathematical analysis made on this basis, plantations differ from each other. Another interesting result is also the spatial distributions of cryptogams on tea bushes resemble those of forest communities and lichens seems to be more sensitive than bryophytes to antropogenic changes of environment.
Phylogenetic analyses using mtSSU and nuITS sequences of Buellia violaceofusca (previously placed in Lecanoromycetes), a sterile, sorediate lichen having a trebouxioid photobiont, surprisingly prove ...that the species is conspecific with Lecanographa amylacea (Arthoniomycetes), a fertile, esorediate species with a trentepohlioid photobiont. These results suggest that L. amylacea and B. violaceofusca are photomorphs of the same mycobiont species, which, depending on the photobiont type, changes the morphology and the reproduction strategy. This is the first example of a lichenized fungus that can select between Trebouxia (Trebouxiophyceae) and trentepohlioid (Ulvophyceae) photobionts. Trebouxia photobionts from the sorediate morphotype belong to at least three different phylogenetic clades, and the results suggest that Lecanographa amylacea can capture the photobiont of other lichens such as Chrysothrix candelaris to form the sorediate morphotype. Phylogenetic analyses based on rbcL DNA data suggest that the trentepohlioid photobiont of L. amylacea is closely related to Trentepohlia isolated from fruticose lichens. The flexibility in the photobiont choice enables L. amylacea to use a larger range of tree hosts. This strategy helps the lichen to withstand changes of environmental conditions, to widen its distribution range and to increase its population size, which is particularly important for the survival of this rare species.
The main aims of this work were to assess phylogenetic relationships of the trentepohlialean photobionts in tropical, mainly sterile, lichens collected in Bolivia, to examine their genetic diversity, ...host specificity, and the impact of habitat factors on the occurrence of Trentepohliales. Based on rbcL marker analysis, we constructed a phylogenetic tree with eight major clades of Trentepohliales, of which seven free‐living species are intermingled with lichenized ones. Our analyses show that the studied photobionts are scattered across the phylogenetic tree and algae from temperate and tropical regions do not form monophyletic groups, except within one clade that seems to be restricted to the tropics. There is no significant occurrence pattern of lichenized Trentepohliaceae on a specific substratum, except Cephaleuros spp. and Phycopeltis spp., which are restricted to leaves, while some clades with lichenized algae may be specialized to tree bark and wood. Moreover, we found two patterns of associations: first, closely related algae can associate with distantly related mycobionts; second, some other trentepohlioid algae associate with selected lineages of fungi (e.g., Arthoniaceae or Graphidaceae). We also found that some lineages of photobionts are even more selective and associate exclusively with one species (e.g., Dichosporidium nigrocinctum, Diorygma antillarum) or closely related lichen‐forming fungi (Herpothallon spp.). Concluding, we found that occurrence of some trentepohlialean photobionts may correlate with the particular type of the mycobiont.
Research highlights: shifts in the composition and functional diversity of lichen biota reflect changes in the environment caused by climate warming and eutrophication. Background and objectives: ...studies on lichen functional diversity and refinement in the functional traits of lichen biota under the pressure of changing environmental factors are currently of great scientific interest. The obtained results are interpreted in relation to specific habitat properties and their modifications due to the potential effects of climate change and atmospheric pollution. The aim of the work was to investigate changes in lichen species composition and functional diversity, as well as to identify factors responsible for them at different forest ecosystem scales. Materials and Methods: we identified factors responsible for changes in lichen biota in a unique Białowieża Forest ecosystem by analyzing shifts in species optima and functional diversity at the forest community, tree phorophyte, and substrate levels. We examined individual lichen species’ responses and temporal shifts in the species composition for each historical and resampled dataset using a community-weighted means of functional lichen traits and Wirth ecological indicator values. Results: the most evident change took place at the level of individual species, which shifted their realized optima: 25 species demonstrated a shift to co-occur with lichens of higher nitrogen demands, 15 demonstrated higher light demands, 14 demonstrated higher temperature preferences, and six demonstrated lower moisture preferences. At the level of forest communities, biota shifted towards the higher proportion of nitrogen-demanding and the lower proportion of moisture-demanding species. At the level of phorophyte species, biota changed towards an increased proportion of lichens of higher temperature preferences. For the substrate level, no directional shifts in lichen species composition were found. Conclusions: climate change has influenced lichen biota in Białowieża Forest, but the main driver of lichen species composition was found to be eutrophication. We suppose that other overlapping factors may contribute to biota shifts, e.g., the extinction and expansion of phorophyte tree species.
In the past few years, new phylogenetic lineages in
were detected as a result of molecular approaches. These studies included symbiont selectivity in lichen communities, transects along altitudinal ...gradients at local and global scales and the photobiont diversity in local populations of lichen-forming fungal species. In most of these studies, phylogenetic and haplotype analyses based on the internal transcribed spacer (ITS) locus have continuously allowed the recognition of new monophyletic lineages, which suggests that still numerous undiscovered
lineages can be hidden in lichens from unexplored areas, especially in the tropics. Here, we estimated the biodiversity of photobionts in Bolivian Andean vegetation and assessed their specificity. About 403 lichen samples representing 42 genera, e.g.,
,
,
,
,
,
,
,
,
, and
, containing
photobionts, were analyzed. ITS ribosomal DNA (rDNA) and
L markers were used. We obtained
sequences from Bolivian samples belonging to already described clades A, C, I, and S. Thirty-nine
lineages were distinguished within these clades, while 16 were new. To reveal the structure of the community of Bolivian photobionts and their relationships with mycobionts, the comparative effects of climate, altitude, geographical distances, substrate, and habitat type, as well as functional traits of lichens such as growth forms, propagation mode and secondary metabolites, were analyzed. Furthermore, new Bolivian records were included in analysis on a global scale. In our study, the mycobiont genus or even species are the most important factors correlated with photobiont identity. Moreover, we revealed that the community of Bolivian photobionts is shaped by altitude.
A tribute to Professor Tor Tønsberg Kukwa, Martin; Ekman, Stefan; Printzen, Christian ...
Plant and fungal systematics (Online),
12/2023, Letnik:
68, Številka:
2
Journal Article
The first records of Parmelia ernstiae from Madeira, as well as the new localities of P. encryptata from Poland and P. sulcata from Chile, are presented. All records are confirmed by molecular data, ...BLAST search, and haplotype network analysis of the nucITS rDNA sequences. The discussion on the morphology and secondary chemistry of all three species is provided with notes on their distribution and similar taxa. Parmelia encryptata is a rarely reported cryptic species that is morphologically indistinguishable from P. sulcata, and its identification requires molecular data. New localities of P. encryptata from northern Poland suggest that the taxon may be widespread in the country and not confined to large forests but also present in open areas on free-standing trees. Moreover, a new nucITS rDNA haplotype of the species is reported. Parmelia ernstiae is a near-cryptic species, morphologically and chemically very similar to P. saxatilis and P. serrana. Two specimens of the species from Madeira have sublinear lobes with marginal and laminal isidia, unlike most specimens of P. ernstiae, having short, broad lobes with laminal isidia, and thus are morphologically closer to P. saxatilis in lobe shape and to P. serrana in placement of isidia. However, the BLAST search and haplotype analysis of nucITS rDNA sequences placed these specimens in P. ernstiae. Parmelia sulcata, a common species in the Northern Hemisphere, is rare elsewhere, and only two records confirmed by molecular data were known from South America. The nucITS rDNA haplotype of two new and two previous records of the species represent the most common haplotype of the species known from the Northern
Hemisphere.
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