M.J. Wingfield’s research while affiliated with University of Pretoria and other places

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Publications (839)


Fungal Planet description sheets: 1697–1780
  • Article
  • Full-text available

December 2024

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1,445 Reads

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4 Citations

Fungal Systematics and Evolution

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M.J. Wingfield

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[...]

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J.Z. Groenewald

Abstract: Novel species of fungi described in this study include those from various countries as follows: Antarctica, Leuconeurospora bharatiensis from accumulated snow sediment sample. Argentina, Pseudocercospora quetri on leaf spots of Luma apiculata. Australia, Polychaetomyces verrucosus on submerged decaying wood in sea water, Ustilaginoidea cookiorum on Scleria levis, Xylaria guardiae as endophyte from healthy leaves of Macaranga tanarius. Belgium, Iodophanus taxi on leaf of Taxus baccata. Belize, Hygrocybe mirabilis on soil. Brazil, Gongronella irregularis from soil, Linodochium splendidum on decaying sheath of Euterpe oleracea, Nothophysalospora agapanthi (incl. Nothophysalospora gen. nov.) on flower stalks of Agapanthus praecox, Phaeosphaeria tabebuiae on leaf ofTabebuia sp., Verrucohypha endophytica (incl. Verrucohypha gen. nov.) from healthy roots of Acrocomia aculeata.Estonia, Inosperma apricum on soil under Quercus robur. Greece, Monosporascus solitarius isolated from surface-sterilised, asymptomatic roots of Microthlaspi perfoliatum. India, Diaporthe neocapsici on young seedling stemsof Capsicum annuum, Fuscoporia naditirana on dead wood, Sebacina spongicarpa on soil, Torula kanvae from the gut of a Copris signatus beetle. Iran, Sarcinomyces pruni from twig and petiole tissues of Prunus persica and Prunus armeniaca, Xenodidymella quercicola from leaf spots of Quercus brantii. Italy, Agaricus aereiceps on grass, Agaricus bellui in meadows, Agaricus fabrianensis in urban grasslands, Beaucarneamyces muscorum on moss growing inforest, Xenoanthostomella quercus on leaf litter of Quercus ilex. Netherlands, Alfaria neerlandica on stem lesions of Cortaderia selloana, Neodictyosporium juncicola on culms of Juncus maritimus, Penicillium geertdesnooi from soil under Papaver rhoeas, Russula abscondita on rich calcareous soil with Quercus, Russula multiseptata on rich claysoil with Quercus, Russula purpureopallescens on soil with Populus, Sarocladium caricicola on leaves of Carex riparia.Pakistan, Circinaria shimlaensis on limestone rocks. Panama, Acrocalymma philodendri on leaf spots of Philodendronsp., Caligospora panamaensis on leaf litter, Chlamydocillium simulans associated with a Xylaria sp., Corynesporina panamaensis on leaf litter, Cylindromonium panamaense on twig litter of angiosperm, Cyphellophora panamaensison twig litter of angiosperm, Microcera panamensis on leaf litter of fern, Pseudotricholoma pusillum in tropicalmontane forest dominated by Quercus spp., Striaticonidium panamaense on leaf litter, Yunnanomyces panamaensison leaf litter. Poland, Albocremella abscondita (incl. Albocremella gen. nov.) from rhizoids of liverwort Conocephalum salebrosum. Portugal, Agaricus occidualis in meadows. South Africa, Alternaria elsarustiae on culms of unidentified Poaceae, Capronia capensis on dead twig of unidentified angiosperm, Codinaeella bulbinicola on dead leaves of Bulbine frutescens, Cytospora carpobroticola on leaf of Carpobrotus quadrifidus, Neophaeomoniella watsoniae on leaf of Watsonia sp., Neoplatysporoides aloigena on leaf of Aloe khamiesensis, Nothodactylaria comitabilis on livingleaf of Itea rhamnoides, Nothopenidiella beaucarneae (incl. Nothopenidiella gen. nov.) on dead leaves of Beaucarnea stricta, Orbilia kirstenboschensis on dead flower stalks of Agapanthus praecox, Phragmocephala agapanthi on dead flower stalks of Agapanthus praecox, Podocarpigena hagahagaensis (incl. Podocarpigena gen. nov.) on leaf spots of Podocarpus falcatus, Sporisorium enterogonipteri from the gut of Gonipterus sp., Synnemapestaloides searsiae on leaf of Searsia populifolia, Xenophragmocapnias diospyri (incl. Xenophragmocapnias gen. nov.) on leaf spots of Diospyros sp., Yunnanomyces hagahagaensis on leaf spots of Sideroxylon inerme. Spain, Agaricus basicinctus in meadows, Agaricus quercetorum among leaf litter in oak forests, Coprinopsis palaciosii on degraded woody debris, Inocybe complutensis in calcareous loamy soil, Inocybe tanitiae in calcareous sandy soil, Mycena subfragosa on dead leaves of Salix atrocinerea, Pseudobaeospora cortegadensis in laurel forests, Trichoderma sedimenticola from fluvial sediments. Sweden, Inocybe badjelanndana on calcareous soil. Ukraine, Beaucarneamyces lupini on overwintered stems of Lupinus polyphyllus, Protocreopsis globulosa on thallus and apothecia of Lecania cyrtella on bark of Populus sp., Thyridium tiliae on dead twigsof Tilia sp. USA, Cladosporium louisianense, Cyphellophora americana from a bedroom vent, Extremus massachusettsianus from lyse buffer, Myxotrichum tapetae on carpet in basement, Neospissiomyces floridanus (incl. Neospissiomyces gen.nov.) on swab from hospital, Polychaetomyces marinus (incl. Polychaetomyces gen. nov.) on submerged driftwood insea water, Steccherinum fragrans on hardwood fallen on the beach, Steinbeckomyces carnegieae (incl. Steinbeckomyces gen. nov.) on Carnegiea gigantea, Tolypocladium pennsylvanicum from air sampled in basement. Vietnam, Acidomyces ducanhii from Aglaia flowers, Acidomyces paludis from dead bark of Acacia sp., Phakopsora sageretiae on Sageretia theezans, Puccinia stixis on Stixis scandens. Morphological and culture characteristics are supported by DNA barcodes.

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Fungal Planet description sheets: 1614–1696

June 2024

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2,545 Reads

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12 Citations

Fungal Systematics and Evolution

Novel species of fungi described in this study include those from various countries as follows: Australia, Baobabopsis sabindy in leaves of Eragrostis spartinoides, Cortinarius magentiguttatus among deep leaf litter, Laurobasidium azarandamiae from uredinium of Puccinia alyxiae on Alyxia buxifolia, Marasmius pseudoelegans on well-rotted twigs and litter in mixed wet sclerophyll and subtropical rainforest. Bolivia, Favolaschia luminosa on twigs of Byttneria hirsuta, Lecanora thorstenii on bark, in savannas with shrubs and trees. Brazil, Asterina costamaiae on leaves of Rourea bahiensis, Purimyces orchidacearum (incl. Purimyces gen. nov.) as root endophyte on Cattleya locatellii. Bulgaria, Monosporascus bulgaricus and Monosporascus europaeus isolated from surface-sterilised, asymptomatic roots of Microthlaspi perfoliatum. Finland, Inocybe undatolacera on a lawn, near Betula pendula. France, Inocybe querciphila in humus of mixed forest. Germany, Arrhenia oblongispora on bare soil attached to debris of herbaceous plants and grasses. Greece, Tuber aereum under Quercus coccifera and Acer sempervirens. India, Alfoldia lenyadriensis from the gut of a Platynotus sp. beetle, Fulvifomes subramanianii on living Albizzia amara, Inosperma pavithrum on soil, Phylloporia parvateya on living Lonicera sp., Tropicoporus maritimus on living Peltophorum pterocarpum. Indonesia, Elsinoe atypica on leaf of Eucalyptus pellita. Italy, Apiotrichum vineum from grape wine, Cuphopyllus praecox among grass. Madagascar, Pisolithus madagascariensis on soil under Intsia bijuga. Netherlands, Cytosporella calamagrostidis and Periconia calamagrostidicola on old leaves of Calamagrostis arenaria, Hyaloscypha caricicola on leaves of Carex sp., Neoniesslia phragmiticola (incl. Neoniesslia gen. nov.) on leaf sheaths of standing dead culms of Phragmites australis, Neptunomyces juncicola on culms of Juncus maritimus, Zenophaeosphaeria calamagrostidis (incl. Zenophaeosphaeria gen. nov.) on culms of Calamagrostis arenaria. Norway, Hausneria geniculata (incl. Hausneria gen. nov.) from a gallery of Dryocoetes alni on Alnus incana. Pakistan, Agrocybe auriolus on leaf litter of Eucalyptus camaldulensis, Rhodophana rubrodisca in nutrient-rich loamy soil with Morus alba. Poland, Cladosporium nubilumfrom hypersaline brine, Entomortierella ferrotolerans from soil at mines and postmining sites, Pseudopezicula epiphylla from sooty mould community on Quercus robur, Quixadomyces sanctacrucensis from resin of Pinus sylvestris, Szafranskia beskidensis (incl. Szafranskia gen. nov.) from resin of Abies alba. Portugal, Ascocoryne laurisilvae on degraded wood of Laurus nobilis, Hygrocybe madeirensis in laurel forests, Hygrocybula terracocta (incl. Hygrocybula gen. nov.) on mossy areas of laurel forests planted with Cryptomeria japonica. Republic of Kenya, Penicillium gorferi from a sterile chicken feather embedded in a soil sample. Slovakia, Cerinomyces tatrensis on bark of Pinus mugo, Metapochonia simonovicovae from soil. South Africa, Acremonium agapanthi on culms of Agapanthus praecox, Alfaria elegiae on culms of Elegia ebracteata, Beaucarneamyces stellenboschensis (incl. Beaucarneamyces gen. nov.) on dead leaves of Beaucarnea stricta, Gardeniomyces kirstenboschensis (incl. Gardeniomyces gen. nov.) rotting fruit of Gardenia thunbergia, Knufia dianellae on dead leaves of Dianella caerulea, Lomaantha quercina on twigs of Quercus suber. Melanina restionis on dead leaves of Restio duthieae, Microdochium buffelskloofinum on seeds of Eragrostis cf. racemosa, Thamnochortomyces kirstenboschensis (incl. Thamnochortomyces gen. nov.) on culms of Thamnochortus fraternus, Tubeufia hagahagana on leaves of Hypoxis angustifolia, Wingfieldomyces cypericola on dead leaves of Cyperus papyrus. Spain, Geastrum federeri in soil under Quercus suber and Q. canariensis, Geastrum nadalii in calcareous soil under Juniperus, Quercus, Cupressus, Pinus and Robinia, Hygrocybe garajonayensis in laurel forests, Inocybe cistophila on acidic soil under Cistus ladanifer, Inocybe sabuligena in a mixed Quercus ilex subsp. ballota/Juniperus thurifera open forest, Mycena calongei on mossy bark base of Juniperus oxycedrus, Rhodophana ulmaria on soil in Ulmus minor forest, Tuber arriacaense in soil under Populus pyramidalis, Volvariella latispora on grassy soils in a Quercus ilex ssp. rotundifolia stand. Sweden, Inocybe iota in alpine heath on calcareous soil. Thailand, Craterellus maerimensis and Craterellus sanbuakwaiensis on laterite and sandy soil, Helicocollum samlanense on scale insects, Leptosporella cassiae on dead twigs of Cassia fistula, Oxydothis coperniciae on dead leaf of Copernicia alba, Russula mukdahanensis on soil, Trechispora sangria on soil, Trechispora sanpatongensis on soil. Türkiye, Amanita corylophila in a plantation of Corylus avellana. Ukraine, Pararthrophiala adonis (incl. Pararthrophiala gen. nov.) on dead stems of Adonis vernalis. USA, Cladorrhinum carnegieae from Carnegiea gigantea, Dematipyriformia americana on swab from basement wall, Dothiora americana from outside air, Dwiroopa aeria from bedroom air, Lithohypha cladosporioides from hospital swab, Macroconia verruculosa on twig of Ilex montana, associated with black destroyed ascomycetous fungus and Biatora sp., Periconia floridana from outside air, Phytophthora fagacearum from necrotic leaves and shoots of Fagus grandifolia, Queenslandipenidiella californica on wood in crawlspace. Morphological and culture characteristics are supported by DNA barcodes.


Colour illustrations. Portugal, Azores, Terceira, Algar do Carvão, laurel forests planted with Cryptomeria japonica, place where the holotype of Geoglossum azoricum was collected.  Right column: apothecia in upper photo correspond with the holotype; middle photo corresponds with: detail of *ascus apex, detail base ascus with crozier (one pictures, H2O) and mature asci (two pictures) in *IKI 2; the bottom photo is *pseudoparaphyses (left) *ectal excipulum (middle) and *medullary excipulum (right) in H2O. Left column: middle photo ascospores (right *RC, left *H2O); the bottom photo is paraphyses (*H2O). * = living. Scale bar = 25 μm (ascospores), 10 μm (all others).
FP1549-1 The most probable maximum likelihood (ML) tree obtained from the ITS + LSU (GenBank accession numbers in FP1549-2) alignment showing
on the branches the ML bootstrap (ML-bs) support values and Bayesian posterior probability (BPP) values (ML-bs/BPP) calculated with IQ-TREE v. 2.1.3
(Nguyen et al. 2015) and MrBayes v. 3.2 (Ronquist et al. 2012), respectively. BPP values ≥ 95 % and ML-bs ≥ 70 % were considered significant. The novel
species is highlighted with a coloured box. Sequences from type material are indicated with (T).
Geoglossum azoricum A. Mateos, De la Peña-Lastra & Plaza, sp. nov.

June 2023

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772 Reads

Persoonia - Molecular Phylogeny and Evolution of Fungi

Geoglossum azoricum A. Mateos, De la Peña-Lastra & Plaza, sp. nov. on mossy areas of laurel forest areas planted with Cryptomeria japonica. Fungal Planet description sheets - Persoonia: 1549



Truncation of MAT1-2-7 Deregulates Developmental Pathways Associated with Sexual Reproduction in Huntiella omanensis

September 2022

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47 Reads

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2 Citations

Microbiology Spectrum

Secondary mating-type genes are being described almost as quickly as new fungal genomes are being sequenced. Understanding the functions of these genes has lagged behind their description, in part due to limited taxonomic distribution, lack of conserved functional domains, and difficulties with regard to genetic manipulation protocols.




Genera of phytopathogenic fungi: GOPHY 4

June 2022

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3,441 Reads

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94 Citations

Studies in Mycology

This paper is the fourth contribution in the Genera of Phytopathogenic Fungi (GOPHY) series. The series provides morphological descriptions and information about the pathology, distribution, hosts and disease symptoms, as well as DNA barcodes for the taxa covered. Moreover, 12 whole-genome sequences for the type or new species in the treated genera are provided. The fourth paper in the GOPHY series covers 19 genera of phytopathogenic fungi and their relatives, including Ascochyta , Cadophora , Celoporthe , Cercospora , Coleophoma , Cytospora , Dendrostoma , Didymella , Endothia , Heterophaeomoniella , Leptosphaerulina , Melampsora , Nigrospora , Pezicula , Phaeomoniella , Pseudocercospora , Pteridopassalora , Zymoseptoria , and one genus of oomycetes, Phytophthora . This study includes two new genera, 30 new species, five new combinations, and 43 typifications of older names.


Generic boundaries in the Ophiostomatales reconsidered and revised

March 2022

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663 Reads

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81 Citations

Studies in Mycology

The Ophiostomatales was erected in 1980. Since that time, several of the genera have been redefined and others have been described. There are currently 14 accepted genera in the Order. They include species that are the causal agents of plant and human diseases and common associates of insects such as bark beetles. Well known examples include the Dutch elm disease fungi and the causal agents of sporotrichosis in humans and animals. The taxonomy of the Ophiostomatales was confused for many years, mainly due to the convergent evolution of morphological characters used to delimit unrelated fungal taxa. The emergence of DNA-based methods has resolved much of this confusion. However, the delineation of some genera and the placement of various species and smaller lineages remains inconclusive. In this study we reconsidered the generic boundaries within the Ophiostomatales . A phylogenomic framework constructed from genome-wide sequence data for 31 species representing the major genera in the Order was used as a guide to delineate genera. This framework also informed our choice of the best markers from the currently most commonly used gene regions for taxonomic studies of these fungi. DNA was amplified and sequenced for more than 200 species, representing all lineages in the Order. We constructed phylogenetic trees based on the different gene regions and assembled a concatenated data set utilising a suite of phylogenetic analyses. The results supported and confirmed the delineation of nine of the 14 currently accepted genera, i.e. Aureovirgo , Ceratocystiopsis , Esteya , Fragosphaeria , Graphilbum , Hawksworthiomyces , Ophiostoma , Raffaelea and Sporothrix . The two most recently described genera, Chrysosphaeria and Intubia , were not included in the multi-locus analyses. This was due to their high sequence divergence, which was shown to result in ambiguous taxonomic placement, even though the results of phylogenomic analysis supported their inclusion in the Ophiostomatales . In addition to the currently accepted genera in the Ophiostomatales , well-supported lineages emerged that were distinct from those genera. These are described as novel genera. Two lineages included the type species of Grosmannia and Dryadomyces and these genera are thus reinstated and their circumscriptions redefined. The descriptions of all genera in the Ophiostomatales were standardised and refined where this was required and 39 new combinations have been provided for species in the newly emerging genera and one new combination has been provided for Sporothrix . The placement of Afroraffaelea could not be confirmed using the available data and the genus has been treated as incertae sedis in the Ophiostomatales . Paleoambrosia was not included in this study, due to the absence of living material available for this monotypic fossil genus. Overall, this study has provided the most comprehensive and robust phylogenies currently possible for the Ophiostomatales . It has also clarified several unresolved One Fungus-One Name nomenclatural issues relevant to the Order.


Citations (75)


... Subsequently, Visagie et al. (2024b) applied GCPSR (Genealogical Concordance Phylogenetic Species Recognition) and phylogenetic analyses to reassess the list of Penicillium species published up to 31 December 2022, resulting in an updated count of 535 species. An additional 100 species of this genus were described from 1 January 2023 to 31 December 2024 (Ansari et al. 2023;Crous et al. 2023;da Silva et al. 2023;Khuna et al. 2023;Li et al. 2023;Liu et al. 2023;Tan 2023;Tan andShivas 2023, 2024;Tan et al. , 2024aTan et al. , 2024bWang et al. 2023;Araújo et al. 2024;Crous et al. 2024;Liang et al. 2024;Lima et al. 2024;Nóbrega et al. 2024;Song et al. 2024;Visagie et al. 2024aVisagie et al. , 2024cZhang et al. 2024). The increase in species numbers in recent years indicates the possibility of numerous undiscovered Penicillium species, and their biodiversity, ecological functions, and potential for resource development warrant further investigation. ...

Reference:

Two new species of Penicillium (Eurotiales, Aspergillaceae) from China based on morphological and molecular analyses
Fungal Planet description sheets: 1697–1780

Fungal Systematics and Evolution

... Moreover, sequences from Greek collections show a relatively high variation (up to 97.5% sequence identity values) compared to the holotypes of the two species. In addition, the existence of T. nitidum in Greece is molecularly confirmed for the first time, while T. aereum is also reported on Andros island, very close to the type locality (Naxos island; [30]). Apart from the four aforementioned taxa, our collections are grouped into three other well-supported phylospecies which were provisionally named T. aff. ...

Fungal Planet description sheets: 1614–1696

Fungal Systematics and Evolution

... It is thus not surprising that a full-length and presumably functional MAT1-2-7 is present in the three heterothallic Huntiella species for which a MAT1-2 genome is available, while being significantly truncated in the three unisexual species. MAT1-2-7 has been experimentally disrupted in H. omanensis and was shown to be essential for sexual reproduction [41,42], however it is unclear what role it plays in the sexual cycle. Further research considering the molecular function and cellular localization of this protein should be conducted to elucidate why the gene is dispensable in homothallic fungi while appearing to be essential in a variety of heterothallic species. ...

Truncation of MAT1-2-7 Deregulates Developmental Pathways Associated with Sexual Reproduction in Huntiella omanensis

Microbiology Spectrum

... flagellaris, and Cercospora sp. G, remained unresolved even with a five-gene phylogenetic analysis (Bakhshi et al., 2015;Bakhshi et al., 2020;Chen et al. 2022). Cercospora species on sugar beet is not an exception. ...

Genera of phytopathogenic fungi: GOPHY 4

Studies in Mycology

... Among the "fungal crops", ambrosia fungi associated with ambrosia beetles (Coleoptera: Scolytinae and, Platypodinae) include the oldest, most widespread, and most species diverse groups. The ability to feed beetle vectors and receive dispersal benefit from them evolved in at least ten groups, of which the most speciose and best studied are the ophiostomatoid ambrosia fungi (Ascomycota: Ophiostomatales) (De Beer et al., 2022), closely followed by Microascales species (Ascomycota: Microascales) (Mayers et al., 2022). However, current research continues to discover an ambrosial lifestyle in many groups where it was previously unknown. ...

Generic boundaries in the Ophiostomatales reconsidered and revised

Studies in Mycology

... This finding is similar to other species of Fusarium (e.g., Vlaardingerbroek et al. 2016) where such dispensable chromosomes have been linked to pathogenicity. Using knock-out mutants, Phasha, Wingfield, Wingfield, Coetzee, Hallen-Adams et al. (2021) showed that fusaric acid plays a role in the aggressiveness of F. circinatum and that the RAS2 protein also plays an important role in the growth and pathogenicity of F. circinatum (Phasha, Wingfield, Wingfield, Coetzee, Hammerbacher, et al. 2021). ...

Deciphering the effect of FUB1 disruption on fusaric acid production and pathogenicity in Fusarium circinatum
  • Citing Article
  • July 2021

Fungal Biology

... Protoplast extraction protocols have been used in the genetic modification of a wide variety of model and non-model fungi. This includes human pathogens (Garre et al., 2015;Zhao et al., 2019), plant pathogens (Antonio et al., 2010;Phasha et al., 2021aPhasha et al., , 2021b, saprobes , mycorrhizal fungi (Wang & Liu, 2013), edible mushrooms (Chang et al., 1985), and mushrooms used in traditional medicinal practices . The widespread utility of protoplasts has, however, been threatened by the everdecreasing availability of the enzymes used to extract these cells. ...

Ras2 is important for growth and pathogenicity in Fusarium circinatum
  • Citing Article
  • February 2021

Fungal Genetics and Biology

... contained data for more than 2500 species, spanning the fungal tree of life, with thousands more genomes currently being sequenced. The collective availability of these resources has revolutionized our knowledge of the ecology, evolution and overall biology of fungi [4][5][6][7][8][9][10][11]. Indeed, genome sequencing has become a routine part of modern fungal research. ...

Fungal genomes enhance our understanding of the pathogens affecting trees cultivated in Southern Hemisphere plantations

Southern Forests: a Journal of Forest Science

... They are also heliophiles, that grow rapidly, are undemanding in terms of soil fertility, and their small fleshy fruits and abundant seeds favour their establishment (Albuquerque et al., 2013;Arzolla et al., 2010;Jansen et al., 2002). Consequently, they are also commonly found in areas where Eucalyptus trees have been established in plantations and where their fungal pathogens potentially threaten plantation forestry (Granados et al., 2020;Gryzenhout et al., 2009;Oliveira et al., 2021;Rêgo et al., 2023;Silva et al., 2023;van der Merwe et al., 2013). The genus Chrysoporthe is one of the most studied genera in the Cryphonectriaceae. ...

Chrysoporthe puriensis sp. nov. from Tibouchina spp. in Brazil: an emerging threat to Eucalyptus
  • Citing Article
  • October 2020

Australasian Plant Pathology

... The fruiting bodies were sectioned (tangentially and vertically) using sterile razor blades and photographed under an Olympus SZX16 stereomicroscope (Tokyo, Japan). The micro-morphological structures were mounted in a drop of 85% lactic acid (Liu et al. 2020) on microscope slides and examined under an Olympus BX53 microscope (Tokyo, Japan). At least 30 replicate measurements were made for each taxonomic character by cellSens imaging software (Olympus, Tokyo, Japan). ...

Reconsideration of species boundaries and proposed DNA barcodes for Calonectria

Studies in Mycology