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-Morphology of Lecanora hagenii (MFLU 16-0605). a, b Ascomata on wood. c Cross section of an ascoma. d Apically branched paraphyses. e, f Asci and paraphyses. g Ellipsoid ascospores. Scale bars: c = 100 µm, d, e, f = 15 µm, g = 10 µm.
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In the present study, lichenized discomycete taxa collected from northern Thailand, southern China, the UK, Ukraine and Russia are documented. Taxonomic studies of these taxa were carried out using both morphology and molecular data. Their phylogenetic relationships were inferred using LSU rDNA and ITS rDNA sequence data or combined analysis of the...
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Word count: 18,563 A dissertation submitted in partial fulfillment of the University of Greenwich's [Computer Security and Forensics] 2 | P a g e ABSTRACT The increasing threat that botnets are representing to the online world at this moment is huge, combined with the skillful hackers from Eastern Europe this problem is not going to disappear too s...
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... In 2022, Letrouitia was placed in the family Brigantiaeaceae (Teloschistales, Lecanoromycetes, Ascomycota, Fungi) [4]. To date, a total of 20 species have been reported, mostly growing epiphytically on bark and occurring mainly in the tropics and subtropics [4][5][6][7][8][9][10]. ...
... Ecology and distribution: Found on bark in tropical rainforests. Previously known only in Thailand [8] and new to China. Description: Thallus grey, greenish to greenish yellow, crustose, smooth, slightly shiny, crack; soredia and isidia absent. ...
... Ecology and distribution: Found on bark in tropical rainforests. Previously known only in Thailand [8] and new to China. ...
Based on morphological, chemical and molecular studies, two new species of the lichen genus Letrouitia are newly described from China. Letrouitia arcuata is distinguished by its arcuate ascospores [8–10(–12)-locular, (28–)33–50(–62.5) × (8–)10–14.5 µm] and L. sinuosa by its ascomata with wavy margins and ascospores with lens-shaped locules [6–8-locular, (18–)19.5–32(–34) × (6.5–)8–14 μm]. In addition, L. magenta is reported for the first time as a new record in China, characterized by small and round ascomata. The descriptions, distribution and phylogenetic analysis of the respective species have been actualized and a key to the Letrouitia species known from China is provided.
... PP). Notes: Stictidaceae was briefly described as having apothecioid to perithecioid ascomata, unbranched paraphyses, cylindrical asci and filamentous ascospores [12,25,37]. Species in this family show high variation in ascospore shape and septation. ...
... cyperi), the asexual morph of which was recorded from the leaves of Cyperaceae in Australia [50]. The sexual morph of F. cyperacearum has been recorded from a dead stem of Clematis subumbellata and Epilobium angustifolium in Thailand [36,37]. Fitzroyomyces is characterized by immersed and cupulate apothecia with a crystalliferous exciple and cylindric-clavate asci with a thickened apex and cylindrical-filiform, multiseptated and hyaline ascospores with one to three deep constrictions, which seemingly contribute to the fragmentation. ...
... The nucleotide differences between Fitzroyomyces hyaloseptisporus and F. pandanicola (HKAS 96206) were 32 bp (3.8%) in LSU (837 bp) and 33 bp (6.1%) in ITS (540 bp) regions. Fitzroyomyces cyperacearum is the only species that was represented by multiple strains (namely MFLU 18-0695b [37], MFLUCC 17-2072 [36] and CBS: 143170 [50]) that have low genetic diversity in the LSU region with 0.4% (5/1010 bp) difference and with 0.6% (4/595 bp) differences in the ITS region, suggesting that there is low intraspecific variation within Fitzroyomyces. Based on the guidance of Jeewon and Hyde [71], a minimum of >1.5% nucleotide differences in the ITS regions may be indicative of a new species. ...
Stictidaceae comprises taxa with diverse lifestyles. Many species in this family are drought resistant and important for studying fungal adaptation and evolution. Stictidaceae comprises 32 genera, but many of them have been neglected for decades due to the lack of field collections and molecular data. In this study, we introduce a new species Fitzroyomyces hyaloseptisporus and a new combination Fitzroyomyces pandanicola. We also provide additional morphological and molecular data for Ostropomyces pruinosellus and O. thailandicus based on new collections isolated from an unidentified woody dicotyledonous host in Chiang Rai, Thailand. Taxonomic conclusions are made with the aid of morphological evidence and phylogenetic analysis of combined LSU, ITS and mtSSU sequence data. Characteristics such as the shape and septation of ascospores and conidia as well as lifestyles among genera of Stictidaceae are discussed.
... et Upreti Type: Huriella loekoesiana S. Y. Kondr. et Upreti Three species of the genus Huriella are hitherto reported in the world(Ekanayaka et al. 2019, 2018b). An additional species new to science is described from India. ...
The present study recorded 36 genera and 115 species of the lichen family Teloschistaceae in India. Three species, i.e. Caloplaca rajasthanica S. Y. Kondr., Upreti et G. P. Sinha, Huriella upretiana S. Y. Kondr., G. K. Mishra, Nayaka et A. Thell, and Squamulea uttarkashiana S. Y. Kondr., Upreti, Nayaka et A. Thell, are described as new species. Seven new combinations, i.e. Fulgogasparrea awasthii (Y. Joshi et Upreti) S. Y. Kondr., Upreti et A. Thell, Neobrownliella cinnabarina (Ach.) S. Y. Kondr., Upreti et A. Thell, Neobrownliella holochracea (Nyl.) S. Y. Kondr., Upreti et A. Thell, Opeltia flavorubescens (Huds.) S. Y. Kondr. et J.-S. Hur, Oxneriopsis bassiae (Willd. ex Ach.) S. Y. Kondr., Upreti et J.-S. Hur, Upretia hueana (B. de Lesd.) S. Y. Kondr. et Upreti and Megaspora subpoliotera (Y. Joshi et Upreti) S. Y. Kondr., Upreti et A. Thell, are proposed based on nrITS phylogeny in the Teloschistaceae and Megasporaceae consequently. Validation of combination Olegblumia demissa is provided. Molecular data on Fulgogasparrea awasthii and Megaspora subpoliotera are recorded from India for the first time. Four new genera including one species each, i.e. Lazarenkoiopsis ussuriensis (Oxner, S. Y. Kondr. et Elix) S. Y. Kondr., L.
Lőkös et J.-S. Hur, Mikhtomia gordejevii (Tomin) S. Y. Kondr., Kärnefelt, Elix, A. Thell, J. Kim, A. S. Kondratiuk et J.-S. Hur, Olegblumia demissa (Flot.) S. Y. Kondr., L. Lőkös, J. Kim, A. S. Kondratiuk, S.-O. Oh et J.-S. Hur and Pachypeltis intrudens (H. Magn.) Søchting, Frödén et Arup, as well as the genus Megaspora are reported as new for the Indian lichen biota.
Out of the eight lichenogeographical regions of India, the Western Himalayas show the maximum diversity of Teloschistaceae members represented with 110 species followed
by the Central Indian region with 38 species. The lichen genus Caloplaca is represented with 50 species in the country followed by Athallia and Rusavskia with 6 species each. The saxicolous taxa exhibit dominance with 65 species whereas the corticolous and erricolous taxa are represented by 48 and 9 species, respectively. Among the different states of India, Uttarakhand showed the maximum diversity represented by 54 species followed by the state of Jammu & Kashmir with 37 species, whereas the Jharkhand and Meghalaya states are represented only by the occurrence of a single species each. A key to the genera and species together with the description, basionyms and synonyms of each species are provided.
Six species of Letrouitia are recorded from the Andaman and Nicobar Islands. Letrouitia flavidula (Tuck.) Hafellner and L. parabola (Nyl.) R. Sant. & Hafellner are reported as new records for India and Letrouitia aureola (Tuck.) Hafellner & Bellem., L. flavocrocea (Nyl.) Hafellner & Bellem. and L. muralis Hafellner as new records for the Andaman and Nicobar Islands.
During the study of the lichen biota of Shikotan Island, Fissurina inabensis (Vain.) M. Nakan. et Kashiw. was identified on the basis of morphological and anatomical data. It is the first record to Russia both at a species and at genus level. The phylogenetic analysis based on the ITS sequences of the studied specimens supported the close relationship with F. insidiosa C. Knight et Mitt. belonging to the subfamily Fissurinoideae. A detailed description of the morphology, anatomy and secondary metabolites of the studied specimens is given. This species was previously known from Japan, Taiwan, and Thailand, and the area is extended to Shikotan Island where are the northernmost localities of the species. Detection of stictic acid might be variable depending on researchers because of the small amount of the substance. It was well detected using HPLC in this study. Differences in the number and size of ascospores in specimens from Shikotan Island and those from Japan described in the literature are discussed.
Humicolopsis cephalosporioides is a soil fungus that is associated with Nothofagus forests in South America. The aim of this study was to analyze the effect of environmental factors such as temperature, light, and nutrition on chlamydospore differentiation as well as pigment biosynthesis. Temperature did not affect chlamydospore production; it rather altered pigmentation development that also was affected by light. The composition of culture media as well as light modulated chlamydospore differentiation. Microscope observations, spectroscopic analysis as well as culture assays, using melanin inhibitors, suggest that the main pigment of chlamydospores of H. cephalosporioides is 1,8 dihydroxynaphthalene (DHN)-melanin–type compound. Furthermore, we found that the genome of H. cephalosporioides contains a sequence highly homologous to the pks sequences of other fungi that have been associated with the biosynthesis of 1,8 DHN-melanin. All this together suggests that melanization is among the most important features linked to survival of this fungus in the soils of Nothofagus forests in sub-Antarctica region and that the ITS, 18S, and 28S rDNA sequences did not provide enough information to delineate the phylogenetic relationships of the fungus within the class Leotiomycetes.
Ostropales sensu lato is a large group comprising both lichenized and non-lichenized fungi, with several lineages expressing optional lichenization where individuals of the same fungal species exhibit either saprotrophic or lichenized lifestyles depending on the substrate (bark or wood). Greatly variable phenotypic characteristics and large-scale phylogenies have led to frequent changes in the taxonomic circumscription of this order. Ostropales sensu lato is currently split into Graphidales, Gyalectales, Odontotrematales, Ostropales sensu stricto, and Thelenellales. Ostropales sensu stricto is now confined to the family Stictidaceae, which includes a large number of species that are poorly known, since they usually have small fruiting bodies that are rarely collected, and thus, their taxonomy remains partly unresolved. Here, we introduce a new genus Ostropomyces to accommodate a novel lineage related to Ostropa, which is composed of two new species, as well as a new species of Sphaeropezia, S. shangrilaensis. Maximum likelihood and Bayesian inference analyses of mitochondrial small subunit spacers (mtSSU), large subunit nuclear rDNA (LSU), and internal transcribed spacers (ITS) sequence data, together with phenotypic data documented by detailed morphological and anatomical analyses, support the taxonomic affinity of the new taxa in Stictidaceae. Ancestral character state analysis did not resolve the ancestral nutritional status of Stictidaceae with confidence using Bayes traits, but a saprotrophic ancestor was indicated as most likely in a Bayesian binary Markov Chain Monte Carlo sampling (MCMC) approach. Frequent switching in nutritional modes between lineages suggests that lifestyle transition played an important role in the evolution of this family.
Eight species, new for science, i.e.: Lobothallia gangwondoana S. Y. Kondr., J.-J. Woo et J.-S. Hur and Phyllopsora dodongensis S. Y. Kondr. et J.-S. Hur from South Korea, Eastern Asia, Ioplaca rinodinoides S. Y. Kondr., K. K. Ingle, D. K. Upreti et S. Nayaka, Letrouitia assamana S. Y. Kondr., G. K. Mishra et D. K. Upreti, and Rusavskia indochinensis S. Y. Kondr., D. K. Upreti et S. Nayaka from India and China, South Asia, Caloplaca orloviana S. Y. Kondr. and Rusavskia drevlyanica S. Y. Kondr. et O. O. Orlov from Ukraine, Eastern Europe, as well as Xanthoria ibizaensis S. Y. Kondr. et A. S. Kondr. from Ibiza Island, Spain, Mediterranean Europe, are described, illustrated and compared with closely related taxa.
Fominiella tenerifensis S. Y. Kondr., Kärnefelt, A. Thell et Feuerer is for the first time recorded from Mediterranean Europe, Huriella loekoesiana S. Y. Kondr. et Upreti is provided from Russia for the first time, and H. pohangensis S. Y. Kondr., L. Lőkös et J.-S. Hur for the first time from China, Phoma candelariellae Z. Kocakaya et Halıcı is new to Ukraine, and Staurothele frustulenta Vain. is recorded from the Forest Zone of Ukraine for the first time.
Twelve new combinations, i.e.: Bryostigma apotheciorum (for Sphaeria apotheciorum A. Massal.), Bryostigma biatoricola (for Arthonia biatoricola Ihlen et Owe-Larss.), Bryostigma dokdoense (for Arthonia dokdoensis S. Y. Kondr., L. Lőkös, B. G. Lee, J.-J. Woo et J.-S. Hur), Bryostigma epiphyscium (for Arthonia epiphyscia Nyl.), Bryostigma lobariellae (for Arthonia lobariellae Etayo), Bryostigma lapidicola (for Lecidea lapidicola Taylor), Bryostigma molendoi (for Tichothecium molendoi Heufl. ex Arnold), Bryostigma neglectulum (for Arthonia neglectula Nyl.), Bryostigma parietinarium (for Arthonia parietinaria Hafellner et Fleischhacker), Bryostigma peltigerinum (for Arthonia vagans var. peltigerina Almq.), Bryostigma phaeophysciae (for Arthonia phaeophysciae Grube et Matzer), Bryostigma stereocaulinum (for Arthonia nephromiaria var. stereocaulina Ohlert), are proposed based on results of combined phylogenetic analysis based on mtSSU and RPB2 gene sequences.
Thirty-one new combinations for members of the genus Polyozosia (i.e.: Polyozosia actophila (for Lecanora actophila Wedd.), Polyozosia agardhiana (for Lecanora agardhiana Ach.), Polyozosia altunica (for Myriolecis altunica R. Mamut et A. Abbas), Polyozosia antiqua (for Lecanora antiqua J. R. Laundon), Polyozosia bandolensis (for Lecanora bandolensis B. de Lesd.), Polyozosia behringii (for Lecanora behringii Nyl.), Polyozosia caesioalutacea (for Lecanora caesioalutacea H. Magn.), Polyozosia carlottiana (for Lecanora carlottiana C. J. Lewis et Śliwa), Polyozosia congesta (for Lecanora congesta Clauzade et Vězda), Polyozosia eurycarpa (for Lecanora eurycarpa Poelt, Leuckert et Cl. Roux), Polyozosia expectans ( Lecanora expectans Darb.), Polyozosia flowersiana ( Lecanora flowersiana H. Magn.), Polyozosia fugiens (for Lecanora fugiens Nyl.), Polyozosia invadens (for Lecanora invadens H. Magn.), Polyozosia juniperina (for Lecanora juniperina Śliwa), Polyozosia latzelii (for Lecanora latzelii Zahlbr.), Polyozosia liguriensis (for Lecanora liguriensis B. de Lesd.), Polyozosia massei (for Myriolecis massei M. Bertrand et J.-Y. Monnat), Polyozosia mons-nivis (for Lecanora mons-nivis Darb.), Polyozosia oyensis (for Lecanora oyensis M.-P. Bertrand et Cl. Roux), Polyozosia percrenata (for Lecanora percrenata H. Magn.), Polyozosia persimilis (for Lecanora hagenii subsp. persimilis Th. Fr.), Polyozosia poeltiana (for Lecanora poeltiana Clauzade et Cl. Roux), Polyozosia prominens (for Lecanora prominens Clauzade et Vězda), Polyozosia prophetae-eliae (for Lecanora prophetae-eliae Sipman), Polyozosia salina (for Lecanora salina H. Magn.), Polyozosia schofieldii (for Lecanora schofieldii Brodo), Polyozosia sverdrupiana (for Lecanora sverdrupiana Øvstedal), Polyozosia torrida (for Lecanora torrida Vain.), Polyozosia wetmorei (for Lecanora wetmorei Śliwa), Polyozosia zosterae (for Lecanora subfusca ? zosterae Ach.)) are proposed.
