The Neotropical species Fomitiporia apiahyna was repeatedly shown to form a lineage with multiple sublineages that could correspond to different phylogenetic species, hence forming a highly diverse species complex. Due to their inconspicuous morphological features, species delimitation in this complex needs an integrative taxonomic perspective. In this study, we have performed multilocus molecular (ITS, ncLSU, TEF-1α, and RPB2) analyses in order to delimit the phylogenetic placement of specimens previously determined as F. apiahyna and to determine the phylogenetic diversity in term of clades that could be equated to species. Both morphological, ecological, and distribution data have been integrated to better delimit species boundaries. The F. apiahyna sensu lato lineage was shown to encompass four clades, corresponding to the four species: F. apiahyna sensu stricto, which is confirmed based on specimens originating from the type locality and here epitypified; F. nubicola sp. nov., proposed based on specimens found on Drimys angustifolia and Drimys sp., a relic plant species distributed exclusively in fragmented forests of high altitude areas in southern Brazil; F. conyana sp. nov., proposed from specimens previously suggested as the closest to F. apiahyna s.s.; and F. murrilli sp. nov., proposed based on specimens found on the locally exotic Eucalyptus sp. and another undefined angiosperm in southern Brazil. Additionally, Phellinus elegans emerged from the synonymy of F. apiahyna and the new combination Fomitiporia elegans is proposed. An identification key to the Neotropical species with pileate basidioma also is provided. Phylogenetically delimited species are strongly supported by ecological data, and in the case of F. conyana by clear-cut morphological data. It is expected that, with the redefinition of F. apiahyna s.s., other phylogenetic species will emerge in the near future.
The potential to produce ethanol and xylitol from xylose by the macro basidiomycete Trametes membranacea was evaluated. All strains studied showed ethanol and xylitol production. The highest ethanol production of xylose was obtained by T. membranacea strain TM158/10 with 5.65 ± 0.21 g/L at pH 4 and 28 °C with 288 h of fermentation and 5.59 ± 0.05 g/L ethanol concentration at pH 5 and 24 °C with 360 h of fermentation. When the conversion was carried out using sugars generated from enzymatic hydrolysis of sugarcane bagasse, there were higher yields from 74 to 15% for ethanol and xylitol, respectively. Although the ethanol and xylitol production need to be optimized, this study showed for the first time the possibility of using T. membranacea for the simultaneous xylitol and ethanol production from pentose sugars, allowing for the possibility of using all released sugars during the hydrolysis of lignocelluloses.
Rineloricaria é caracterizado por uma ampla variabilidade cromossômica e relatos de polimorfismos numéricos e/ou estruturais são relativamente comuns para este gênero. A bacia do Rio Iguaçu, a qual pertence a população em estudo, caracteriza-se por uma ictiofauna endêmica tornando-a de grande interesse para estudos filogenéticos e evolutivos. Estudos prévios realizados para uma população do Rio Iguaçu no estado do Paraná, revelaram um expressivo polimorfismo cromossômico numérico e estrutural de 2n=64 a 68, com diversas fórmulas cariotípica em Rineloricaria aff. langei. Sendo assim, com a finalidade de investigar se há mais de uma espécie para a população em estudo, foi sequenciado gene mitocondrial Citocromo C Oxidase I (COI) de 12 indivíduos pertencentes a população de Rineloricaria aff. langei. O COI foi isolado através da amplificação com primers específicos gerando fragmentos de aproximadamente 500 pb. Analises filogenéticas utilizando os métodos de máxima verossimilhança e analise bayesiana evidenciaram a distinção de dois clados para esta população, com divergência genética média acima de 3%. O clado 1 agrupou 8 cariótipos prováveis: cariótipo A com 2n= 65, fórmula cariotípica 3m+62st/a e NF=68, B com 2n=65, 4m+61st/a e NF=69, C com 2n=66, 3m+63st/a e NF=69, D com 2n=67, 3m+64st/a e NF=70, E com 2n=65, 4m+61st/a e NF=69, F com 2n=67, 4m+63st/a e NF=71, G com 2n=67, 1m+66st/a e NF=68 e H com 2n=67, 2m+65st/a e NF=69. Enquanto, o clado 2 agrupou 4 cariótipos: cariótipo I com 2n=66, 2m+64st/a e NF=68, J com 2n=65, 3m+62st/a e NF=68, K com 2n=65, 6m+59st/a e NF=71, e L com 2n=67, 3m+64st/a e NF=70. Os dados moleculares, obtidos no presente estudo, suportam a hipótese de novas espécies, as quais podem estar envolvidas em um mecanismo de diferenciação de espécies decorrente de rearranjos cromossômicos tais como, translocação e/ou fusão e que, embora seja um polimorfismo extenso, a manutenção deste seja garantida pelos cruzamentos entre os indivíduos, com formação de gametas viáveis e que se perpetuam na população dado as características comportamentais sedentárias desta espécie.Suporte financeiro: CAPES – PBC/UEM
The genus Parapterulicium was first introduced to accommodate two Brazilian species of coralloid fungi with affinities to Pterulaceae (Agaricales). Despite the coralloid habit and the presence of skeletal hyphae, other features, notably the presence of gloeocystidia, dichophyses and papillate hyphal ends, differentiate this genus from Pterulaceaesensu stricto. Fieldwork in Brazil resulted in the rediscovery of two coralloid fungi identifiable as Parapterulicium, the first verified collections of this genus since Corner's original work in the 1950s. Molecular phylogenetic analyses of nrITS and nrLSU sequences from these modern specimens revealed affinities with the /peniophorales clade in the Russulales, rather than Pterulaceae. The presence of distinctive hyphal elements, homologous to the defining features of /peniophorales, is consistent with the phylogenetic evidence and thus clearly distinguished Parapterulicium and its type species P.subarbusculum from Pterulaceae, placing this genus within /peniophorales. Parapterulicium was also found to be polyphyletic so Baltazaria gen. nov. is proposed to accommodate P.octopodites, Scytinostromagalactinum, S.neogalactinum and S.eurasiaticogalactinum also within /peniophorales.
Ophiocordyceps nutans is an entomogenous fungus growing on true bugs (Hemiptera), which has a presumed worldwide distribution. During forays of entomogenous fungi in Brazil, specimens morphologically similar to O. nutans were collected from the Atlantic Forest and Cerrado domains of Neotropical region. Morphological comparisons, as well as molecular phylogenetic analyses using ITS, led us to conclude that the neotropical specimens represent a new species Ophiocordyceps neonutans . The Neotropical occurrence of this taxon and its taxonomic implications are re-evaluated here. We discuss O. nutans as a species complex with distinct geographic lineages and host specificity. In addition, Barcoding gap analysis suggests that the different lineages have a great genetic distance between them.
Morphological revision of Fulvifomes robiniae , as well as phylogenetic inferences based on nITS and nLSU markers, indicated that the species has a narrower concept in its morphology and distribution. Other morphologically related taxa arise from this taxonomic approach. Fulvifomes cedrelae is not accepted as a synonym of F. robiniae , and Fulvifomes squamosus sp. nov. is described as new based on Peruvian specimens. Based on morphology, phylogenetic relationships and host distributions, the taxonomic implication for the genus and other related taxa are discussed.
Insect-fungal interactions are an important but understudied aspect of tropical forest ecology. Here we present the first large-scale study of insect communities feeding on the reproductive structures of macrofungi (basidiomes) in the Neotropics. This trophic interaction is not well characterized in most ecosystems; however, beetle consumption of basidiomes is thought to be affected by fungal factors, via mechanisms analogous to those observed in plant-herbivore interactions and in some interactions with fungi as hosts in the Holarctic region. We investigated how the composition of beetle assemblages varies as a function of fungal taxonomic distance, basidiome consistency, and hyphal systems. We collected 367 basidiomes belonging to the orders Polyporales and Hymenochaetales in the subtropical Araucaria angustifolia forest region of southern Brazil, along with any fauna present or without it. Basidiomes were maintained individually in the laboratory in plastic containers for up to three months to allow beetles to develop to adulthood, at which point the beetles were collected. We found that 207 basidiome specimens representing 40 species were associated with beetles. We recorded 447 occurrences of Coleoptera, representing 90 morphospecies from 20 families. We found that assemblages of fungivorous Coleoptera were more similar among more closely related fungi. Furthermore, the beetle assemblages varied as a function of basidiome toughness, which is influenced by sporocarp consistency and hyphal system type. The associations between beetles and basidiomes resemble those reported previously in temperate zones, suggesting continuity in the structure of such associations across a wide latitudinal range.
During fungal surveys in a small urban Protected Area in Southern Brazil a species of Phylloporia was found with its minute basidiomata emerging from living stems of Doliocarpus schottianus. It is characterized by pileate and strikingly small basidiomata, context with a black line separating an upper tomentum, 3–7(–8) pores per mm, a monomitic hyphal system and ellipsoid basidiospores. In phylogenetic analysis based on partial nuclear 28S ribosomal DNA sequences, these specimens are resolved as a new clade within Phylloporia. The species is therefore described as P. minuta sp. nov. Ecological data (host and distribution) and the importance of small and urban protected areas are discussed
The Atlantic Forest of Brazil harbors a great diversity of boletoid fungi, many of which remain to be documented and described. Two distinct taxa of Tylopilus from Northeastern Atlantic Forest, T. dunensis and T. pygmaeus, are proposed as new based on evidence from both morphological and molecular data. We provide detailed macro- and microscopic descriptions of each species including scanning electron micrographs of the basidiospores.
Polyporus dictyopus, with a large number of heterotypic synonyms, has been traditionally considered a species complex, characterized by wide morphological variation and geographic distribution. Thus, neotropical specimens previously identified as P. dictyopus from Amazonia, Cerrado and Atlantic Forest biomes were studied based on detailed macro-and micromorphological examination and phylogenetic analyses, using distinct ribosomal and protein-coding genomic regions: the nuclear ribosomal internal transcribed spacer (nrITS), nuclear ribosomal large subunit (nrLSU), and RNA polymerase II second subunit (RPB2). Two unrelated generic lineages, each one represented by different species, are reported: Atroporus is recovered and re-circumscribed to include A. diabolicus and A. rufoatratus comb. nov.; Neodictyopus gen. nov. is proposed to accommodate N. dictyopus comb. nov. and two new species, N. atlanticae and N. gugliottae. Our study showed that at least five distinct species were hidden under the name P. dictyopus. Detailed descriptions, pictures, illustrations, and a key are provided for Atroporus and Neodictyopus species.
Phallus aureolatus, a new gasteroid species found in the Atlantic Rainforest in Brazil, is herein described, illustrated and its phylogenetic affinities are discussed. This new species is characterized by a pinkish volva, rhizomorphs with purplish pigments, a long white indusium, and a merulioid receptacle with a prominent, pseudoparenchymatous cap on the top when just exposed. A comparison with the morphologically similar taxa is presented, and a key to identify species of Phallus sensu lato (s.l.) known to occur in Brazil is provided.
During a taxonomic revision of species belonging to Phylloporia, some collections from the Atlantic Forest of southern Brazil previously determined as P. spathulata had morphological discrepancies in comparison to the type material of this taxon. Both molecular phylogenetic and morphological analysis revealed them to be two distinct species, described here as Phylloporia elegans sp. nov. and P. nodostipitata sp. nov. They mainly differ from P. spathulata by having reviving basidiomata with smaller pores and basidiospores. Phylloporia nodostipitata develops caespitose basidiomata with a knotted and flexuous stipe and a tomentose pileal surface. Phylloporia elegans develops solitary basidiomata with a cylindrical and straight stipe and a plagiotrichoderm pileal surface. Both species are described, illustrated, discussed and compared with Phylloporia spathulata based on a study of the type. Phylloporia spathulata sensu stricto is presented based on its basionym type material.
A new poroid genus with two conspicuous and common species growing on living Fabaceae trees is described from the Seasonally Dry Tropical Forests biome of Brazil. Both taxa in this forest pathogen genus resemble Phellinus rimosus macroscopically, but are distinguished by a dimitic hyphal system with skeletal hyphae present only in the trama of the tube layer while the context remains monomitic, and by the ellipsoid, thick- walled, adaxially flattened, yellow basidiospores that turn chestnut brown in KOH solution. Molecular and morphological studies of Brazilian specimens macroscopically similar to the Phellinus rimosus species complex were carried out to solve their phylogenetic relationships among the Hymenochaetaceae. Phellinotus gen. nov. with P. neoaridus sp. nov. as the genus type and P. piptadeniae comb. nov. are presented and described. Phylogenetically, Phellinotus is closely related to Arambarria, Inocutis, Fomitiporella and other taxonomically unresolved terminal clades, and unrelated to Fulvifomes and Phylloporia. Phellinotus and other genera of poroid Hymenochaetaceae that lack setae or setal hyphae and produce thick- walled, colored (pale yellow to rusty brown) basidiospores form a phylogenetic group here named the 'phellinotus clade'. Our results indicate the need to include taxa from unexplored areas in order to get a thorough understanding of the phylogeny of the Hymenochaetaceae.
This is a continuity of a series of taxonomic papers where materials are examined, described and novel combinations are proposed where necessary to improve our traditional species concepts and provide updates on their classification. In addition to extensive morphological descriptions and appropriate asexual and sexual connections, DNA sequence data are also analysed from concatenated datasets (rDNA, TEF-α, RBP2 and β-Tubulin) to infer phylogenetic relationships and substantiate systematic position of taxa within appropriate ranks. Wherever new species or combinations are being proposed, we apply an integrative approach (morphological and molecular data as well as ecological features wherever applicable). Notes on 125 fungal taxa are compiled in this paper, including eight new genera, 101 new species, two new combinations, one neotype, four reference specimens, new host or distribution records for eight species and one alternative morphs. The new genera introduced in this paper are Alloarthopyrenia, Arundellina, Camarosporioides, Neomassaria, Neomassarina, Neotruncatella, Paracapsulospora and Pseudophaeosphaeria. The new species are Alfaria spartii, Alloarthopyrenia italica, Anthostomella ravenna, An. thailandica, Arthrinium paraphaeospermum, Arundellina typhae, Aspergillus koreanus, Asterina cynometrae, Bertiella ellipsoidea, Blastophorum aquaticum, Cainia globosa, Camarosporioides phragmitis, Ceramothyrium menglunense, Chaetosphaeronema achilleae, Chlamydotubeufia helicospora, Ciliochorella phanericola, Clavulinopsis aurantiaca, Colletotrichum insertae, Comoclathris italica, Coronophora myricoides, Cortinarius fulvescentoideus, Co. nymphatus, Co. pseudobulliardioides, Co. tenuifulvescens, Cunninghamella gigacellularis, Cyathus pyristriatus, Cytospora cotini, Dematiopleospora alliariae, De. cirsii, Diaporthe aseana, Di. garethjonesii, Distoseptispora multiseptata, Dis. tectonae, Dis. tectonigena, Dothiora buxi, Emericellopsis persica, Gloniopsis calami, Helicoma guttulatum, Helvella floriforma, H. oblongispora, Hermatomyces subiculosa, Juncaceicola italica, Lactarius dirkii, Lentithecium unicellulare, Le. voraginesporum, Leptosphaeria cirsii, Leptosphaeria irregularis, Leptospora galii, Le. thailandica, Lindgomyces pseudomadisonensis, Lophiotrema bambusae, Lo. fallopiae, Meliola citri-maximae, Minimelanolocus submersus, Montagnula cirsii, Mortierella fluviae, Muriphaeosphaeria ambrosiae, Neodidymelliopsis ranunculi, Neomassaria fabacearum, Neomassarina thailandica, Neomicrosphaeropsis cytisi, Neo. cytisinus, Neo. minima, Neopestalotiopsis cocoës, Neopestalotiopsis musae, Neoroussoella lenispora, Neotorula submersa, Neotruncatella endophytica, Nodulosphaeria italica, Occultibambusa aquatica, Oc. chiangraiensis, Ophiocordyceps hemisphaerica, Op. lacrimoidis, Paracapsulospora metroxyli, Pestalotiopsis sequoiae, Peziza fruticosa, Pleurotrema thailandica, Poaceicola arundinis, Polyporus mangshanensis, Pseudocoleophoma typhicola, Pseudodictyosporium thailandica, Pseudophaeosphaeria rubi, Purpureocillium sodanum, Ramariopsis atlantica, Rhodocybe griseoaurantia, Rh. indica, Rh. luteobrunnea, Russula indoalba, Ru. pseudoamoenicolor, Sporidesmium aquaticivaginatum, Sp. olivaceoconidium, Sp. pyriformatum, Stagonospora forlicesenensis, Stagonosporopsis centaureae, Terriera thailandica, Tremateia arundicola, Tr. guiyangensis, Trichomerium bambusae, Tubeufia hyalospora, Tu. roseohelicospora and Wojnowicia italica. New combinations are given for Hermatomyces mirum and Pallidocercospora thailandica. A neotype is proposed for Cortinarius fulvescens. Reference specimens are given for Aquaphila albicans, Leptospora rubella, Platychora ulmi and Meliola pseudosasae, while new host or distribution records are provided for Diaporthe eres, Di. siamensis, Di. foeniculina, Dothiorella iranica, Do. sarmentorum, Do. vidmadera, Helvella tinta and Vaginatispora fuckelii, with full taxonomic details. An asexual state is also reported for the first time in Neoacanthostigma septoconstrictum. This paper contributes to a more comprehensive update and improved identification of many ascomycetes and basiodiomycetes.