Manuela Dal Forno

Dr. Manuela Dal Forno


Research Focus & Metrics

Academic Career Length

18Years (2009-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
6 November 2015 in Fungal Diversity
Verified
Journal Article
Closed access
PDF file
Hiran AriyawansaHiran Ariyawansa
Hiran Ariyawansa
KHKevin D. Hyde
Kevin D. Hyde
SJSubashini C. Jayasiri
Subashini C. Jayasiri
BBBart Buyck
Bart Buyck
TWThilini Chethana Kandawatte Wedaralalage
Thilini Chethana Kandawatte Wedaralalage
HEHernawati
Hernawati
This paper is a compilation of notes on 142 fungal taxa, including five new families, 20 new genera, and 100 new species, representing a wide taxonomic and geographic range. The new families, Ascocylindricaceae, Caryosporaceae and Wicklowiaceae (Ascomycota) are introduced based on their distinct lineages and unique morphology. The new Dothideomycete genera Pseudomassariosphaeria (Amniculicolaceae), Heracleicola, Neodidymella and Pseudomicrosphaeriopsis (Didymellaceae), Pseudopithomyces (Didymosphaeriaceae), Brunneoclavispora, Neolophiostoma and Sulcosporium (Halotthiaceae), Lophiohelichrysum (Lophiostomataceae), Galliicola, Populocrescentia and Vagicola (Phaeosphaeriaceae), Ascocylindrica (Ascocylindricaceae), Elongatopedicellata (Roussoellaceae), Pseudoasteromassaria (Latoruaceae) and Pseudomonodictys (Macrodiplodiopsidaceae) are introduced. The newly described species of Dothideomycetes (Ascomycota) are Pseudomassariosphaeria bromicola (Amniculicolaceae), Flammeascoma lignicola (Anteagloniaceae), Ascocylindrica marina (Ascocylindricaceae), Lembosia xyliae (Asterinaceae), Diplodia crataegicola and Diplodia galiicola (Botryosphaeriaceae), Caryospora aquatica (Caryosporaceae), Heracleicola premilcurensis and Neodidymella thailandicum (Didymellaceae), Pseudopithomyces palmicola (Didymosphaeriaceae), Floricola viticola (Floricolaceae), Brunneoclavispora bambusae, Neolophiostoma pigmentatum and Sulcosporium thailandica (Halotthiaceae), Pseudoasteromassaria fagi (Latoruaceae), Keissleriella dactylidicola (Lentitheciaceae), Lophiohelichrysum helichrysi (Lophiostomataceae), Aquasubmersa japonica (Lophiotremataceae), Pseudomonodictys tectonae (Macrodiplodiopsidaceae), Microthyrium buxicola and Tumidispora shoreae (Microthyriaceae), Alloleptosphaeria clematidis, Allophaeosphaeria cytisi, Allophaeosphaeria subcylindrospora, Dematiopleospora luzulae, Entodesmium artemisiae, Galiicola pseudophaeosphaeria, Loratospora luzulae, Nodulosphaeria senecionis, Ophiosphaerella aquaticus, Populocrescentia forlicesenensis and Vagicola vagans (Phaeosphaeriaceae), Elongatopedicellata lignicola, Roussoella magnatum and Roussoella angustior (Roussoellaceae) and Shrungabeeja longiappendiculata (Tetraploasphaeriaceae). The new combinations Pseudomassariosphaeria grandispora, Austropleospora archidendri, Pseudopithomyces chartarum, Pseudopithomyces maydicus, Pseudopithomyces sacchari, Vagicola vagans, Punctulariopsis cremeoalbida and Punctulariopsis efibulata Dothideomycetes. The new genera Dictyosporella (Annulatascaceae), and Tinhaudeus (Halosphaeriaceae) are introduced in Sordariomycetes (Ascomycota) while Dictyosporella aquatica (Annulatascaceae), Chaetosphaeria rivularia (Chaetosphaeriaceae), Beauveria gryllotalpidicola and Beauveria loeiensis (Cordycipitaceae), Seimatosporium sorbi and Seimatosporium pseudorosarum (Discosiaceae), Colletotrichum aciculare, Colletotrichum fusiforme and Colletotrichum hymenocallidicola (Glomerellaceae), Tinhaudeus formosanus (Halosphaeriaceae), Pestalotiopsis subshorea and Pestalotiopsis dracaenea (Pestalotiopsiceae), Phaeoacremonium tectonae (Togniniaceae), Cytospora parasitica and Cytospora tanaitica (Valsaceae), Annulohypoxylon palmicola, Biscogniauxia effusae and Nemania fusoideis (Xylariaceae) are introduced as novel species to order Sordariomycetes. The newly described species of Eurotiomycetes are Mycocalicium hyaloparvicellulum (Mycocaliciaceae). Acarospora septentrionalis and Acarospora castaneocarpa (Acarosporaceae), Chapsa multicarpa and Fissurina carassensis (Graphidaceae), Sticta fuscotomentosa and Sticta subfilicinella (Lobariaceae) are newly introduced in class Lecanoromycetes. In class Pezizomycetes, Helvella pseudolacunosa and Helvella rugosa (Helvellaceae) are introduced as new species. The new families, Dendrominiaceae and Neoantrodiellaceae (Basidiomycota) are introduced together with a new genus Neoantrodiella (Neoantrodiellaceae), here based on both morphology coupled with molecular data. In the class Agaricomycetes, Agaricus pseudolangei, Agaricus haematinus, Agaricus atrodiscus and Agaricus exilissimus (Agaricaceae), Amanita melleialba, Amanita pseudosychnopyramis and Amanita subparvipantherina (Amanitaceae), Entoloma calabrum, Cora barbulata, Dictyonema gomezianum and Inocybe granulosa (Inocybaceae), Xerocomellus sarnarii (Boletaceae), Cantharellus eucalyptorum, Cantharellus nigrescens, Cantharellus tricolor and Cantharellus variabilicolor (Cantharellaceae), Cortinarius alboamarescens, Cortinarius brunneoalbus, Cortinarius ochroamarus, Cortinarius putorius and Cortinarius seidlii (Cortinariaceae), Hymenochaete micropora and Hymenochaete subporioides (Hymenochaetaceae), Xylodon ramicida (Schizoporaceae), Colospora andalasii (Polyporaceae), Russula guangxiensis and Russula hakkae (Russulaceae), Tremella dirinariae, Tremella graphidis and Tremella pyrenulae (Tremellaceae) are introduced. Four new combinations Neoantrodiella gypsea, Neoantrodiella thujae (Neoantrodiellaceae), Punctulariopsis cremeoalbida, Punctulariopsis efibulata (Punctulariaceae) are also introduced here for the division Basidiomycota. Furthermore Absidia caatinguensis, Absidia koreana and Gongronella koreana (Cunninghamellaceae), Mortierella pisiformis and Mortierella formosana (Mortierellaceae) are newly introduced in the Zygomycota, while Neocallimastix cameroonii and Piromyces irregularis (Neocallimastigaceae) are introduced in the Neocallimastigomycota. Reference specimens or changes in classification and notes are provided for Alternaria ethzedia, Cucurbitaria ephedricola, Austropleospora, Austropleospora archidendri, Byssosphaeria rhodomphala, Lophiostoma caulium, Pseudopithomyces maydicus, Massariosphaeria, Neomassariosphaeria and Pestalotiopsis montellica.

18 February 2011 in Phytotaxa
Verified
Journal Article
Open access
PDF file
HLHelge Thorsten Lumbsch
Helge Thorsten Lumbsch
TAT. Ahti
T. Ahti
SAS. Altermann
S. Altermann
GPGuillermo Amo De Paz
Guillermo Amo De Paz
AAAndre Aptroot
Andre Aptroot
RLR. Lucking
R. Lucking
One hundred new species of lichenized fungi: a signature of undiscovered global diversity

30 June 2014 in Proceedings of the National Academy of Sciences
Verified
Journal Article
Closed access
PDF file
RLRobert Lücking
Robert Lücking
MFManuela Dal Forno
Manuela Dal Forno
MSMasoumeh Sikaroodi
Masoumeh Sikaroodi
PGPatrick M. Gillevet
Patrick M. Gillevet
FBFrank Bungartz
Frank Bungartz
JLJames D. Lawrey
James D. Lawrey
Significance: Macrolichens are considered to be well known, including the tropical montane basidiolichen fungus Dictyonema glabratum , also known as Cora pavonia , an important component of threatened paramo ecosystems, where it acts as a biological fertilizer due to its ability to fix atmospheric nitrogen. This lichen was long believed to represent a single species, but after revising this number to 16 in two genera ( Cora and Corella ), here we show that at least 126 phylogenetically and morphologically distinct species are contained within this group, with statistical analysis predicting more than 400. Our findings underline the importance of accurately documenting species richness for conservation purposes and support the notion of neotropical paramos as hotspots of recent diversification in plants, animals, and fungi.

3 October 2016 in Fungal Diversity
Verified
Journal Article
Closed access
PDF file
RLRobert Lücking
Robert Lücking
MFManuela Dal Forno
Manuela Dal Forno
BMBibiana Moncada
Bibiana Moncada
LCLuis Fernando Coca
Luis Fernando Coca
LVLeidy Yasmín Vargas-Mendoza
Leidy Yasmín Vargas-Mendoza
JLJames D. Lawrey
James D. Lawrey
Following a large-scale phylogenetic study of the lichenized genus Cora (Basidiomycota: Agaricales: Hygrophoraceae), we formally describe 70 new species, honouring the seventieth birthday of David Leslie Hawksworth, one of the preeminent figures in mycology and lichenology in the past 50 years. Based on an updated phylogeny using the ITS fungal barcoding locus, we now recognize 189 taxa in a genus that until recently was considered to represent a single species; including this contribution, 92 of these are formally recognized, including five taxa based on historical names or collections that have not been sequenced. Species of Cora can be recognized by a combination of morphological (size, colour, lobe configuration, surface hairs, hymenophore size and shape), anatomical (thallus thickness, cortex structure, photobiont type, hyphal papillae), and ecogeographical features (substrate, habitat, distribution), and a keytable allowing the identification of all accepted taxa is provided. The new species are: Cora accipiter Moncada, Madriñán & Lücking spec. nov., C. applanata Moncada, Soto-Medina & Lücking spec. nov., C. arachnodavidea Moncada, Dal Forno & Lücking spec. nov., C. arborescens Dal Forno, Chaves & Lücking spec. nov., C. arcabucana Moncada, C. Rodríguez & Lücking spec. nov., C. aturucoa Lücking, Moncada & C. Vargas spec. nov., C. auriculeslia Moncada, Yánez-Ayabaca & Lücking spec. nov., C. barbifera Moncada, Patiño & Lücking spec. nov., C. boleslia Lücking, E. Morales & Dal Forno spec. nov., C. caliginosa Holgado, Rivas Plata & Perlmutter spec. nov., C. campestris Dal Forno, Eliasaro & Spielmann spec. nov., C. canari Nugra, Dal Forno & Lücking spec. nov., C. caraana Lücking, Martins & Lucheta spec. nov., C. casasolana Moncada, R.-E. Pérez & Lücking spec. nov., C. caucensis Moncada, M. Gut. & Lücking spec. nov., C. celestinoa Moncada, Cabrera-Amaya & Lücking spec. nov., C. comaltepeca Moncada, R.-E. Pérez & Herrera-Camp. spec. nov., C. corani Lücking, E. Morales & Dal Forno spec. nov., C. corelleslia Moncada, A. Suárez-Corredor & Lücking spec. nov., C. crispoleslia Moncada, J. Molina & Lücking spec. nov., C. cuzcoensis Holgado, Rivas Plata & Perlmutter spec. nov., C. dalehana Moncada, Madriñán & Lücking spec. nov., C. davibogotana Lücking, Moncada & Coca spec. nov., C. davicrinita Moncada, Madriñán & Lücking spec. nov., C. davidia Moncada, L. Vargas & Lücking spec. nov., C. dewisanti Moncada, A. Suárez-Corredor & Lücking spec. nov., C. dulcis Moncada, R.-E. Pérez & Lücking spec. nov., C. elephas Lücking, Moncada & L. Vargas spec. nov., C. fuscodavidiana Lücking, Moncada & L. Vargas spec. nov., C. garagoa Simijaca, Moncada & Lücking spec. nov., C. gigantea Lücking, Moncada & Coca spec. nov., C. gomeziana Dal Forno, Chaves & Lücking spec. nov., C. guajalitensis Lücking, Robayo & Dal Forno spec. nov., C. hafecesweorthensis Moncada, Lücking & R. Peláez spec. nov., C. haledana Dal Forno, Chaves & Lücking spec. nov., C. hawksworthiana Dal Forno, P. Nelson & Lücking spec. nov., C. hochesuordensis Lücking, E. Morales & Dal Forno spec. nov., C. hymenocarpa Lücking, Chaves & Lawrey spec. nov., C. imi Lücking, Chaves & Lawrey spec. nov., C. itabaiana Dal Forno, Aptroot & M. Cáceres spec. nov., C. leslactuca Lücking, Moncada & R. Peláez spec. nov., C. maxima Wilk, Dal Forno & Lücking spec. nov., C. minutula Lücking, Moncada & Yánez-Ayabaca spec. nov., C. palaeotropica Weerakoon, Aptroot & Lücking spec. nov., C. palustris Dal Forno, Chaves & Lücking spec. nov., C. parabovei Dal Forno, Kukwa & Lücking spec. nov., C. paraciferrii Lücking, Moncada & J.E. Hern. spec. nov., C. paraminor Dal Forno, Chaves & Lücking spec. nov., C. pastorum Moncada, Patiño & Lücking spec. nov., C. pichinchensis Paredes, Jonitz & Dal Forno spec. nov., C. pikynasa J.-M. Torres, Moncada & Lücking spec. nov., C. pseudobovei Wilk, Dal Forno & Lücking spec. nov., C. pseudocorani Lücking, E. Morales & Dal Forno spec. nov., C. putumayensis L.J. Arias, Moncada & Lücking spec. nov., C. quillacinga Moncada, F. Ortega & Lücking spec. nov., C. rothesiorum Moncada, Madriñán & Lücking spec. nov., C. rubrosanguinea Nugra, Moncada & Lücking spec. nov., C. santacruzensis Dal Forno, Bungartz & Yánez-Ayabaca, spec. nov., C. schizophylloides Moncada, C. Rodríguez & Lücking spec. nov., C. smaragdina Lücking, Rivas Plata & Chaves spec. nov., C. soredavidia Dal Forno, Marcelli & Lücking spec. nov., C. subdavicrinita Moncada, J. Molina & Lücking spec. nov., C. suturifera Nugra, Besal & Lücking spec. nov., C. terrestris Dal Forno, Chaves & Lücking spec. nov., C. terricoleslia Wilk, Dal Forno & Lücking spec. nov., C. udebeceana Moncada, R. Peláez & Lücking spec. nov., C. urceolata Moncada, Coca & Lücking spec. nov., C. verjonensis Lücking, Moncada & Dal Forno spec. nov., C. viliewoa Lücking, Chaves & Soto-Medina spec. nov., and C. yukiboa Mercado-Díaz, Moncada & Lücking spec. nov. Furthermore, the taxonomic status of the recently described or recognized species C. arachnoidea, C. aspera, C. ciferrii, and C. reticulifera, is revised.

20 April 2017 in Fungal Diversity
Verified
Journal Article
Closed access
PDF file
MFManuela Dal Forno
Manuela Dal Forno
FBFrank Bungartz
Frank Bungartz
AYAlba Yánez-Ayabaca
Alba Yánez-Ayabaca
RLRobert Lücking
Robert Lücking
JLJames D. Lawrey
James D. Lawrey
This study is a re-assessment of basidiolichen diversity in the Galapagos Islands. We present a molecular phylogenetic analysis, based on 92 specimens from Galapagos, using two nuclear ribosomal DNA markers (ITS and nuLSU). We also re-examined the morphology and anatomy of all sequenced material. The molecular results confirm our previous assessment that all Galapagos basidiolichens belong to the Dictyonema clade, which in Galapagos is represented by four genera: Acantholichen, Cora, Cyphellostereum, and Dictyonema. Most species previously reported from Galapagos in these genera were at the time believed to represent widely distributed taxa. This conclusion, however, has changed with the inclusion of molecular data. Although almost the same number of species is distinguished, the phylogenetic data now suggest that all are restricted to the Galapagos Islands. Among them, six species are proposed here as new to science, namely Cora galapagoensis, Cyphellostereum unoquinoum, Dictyonema barbatum, D. darwinianum, D. ramificans, and D. subobscuratum; and four species have already been described previously, namely Acantholichen galapagoensis, Cora santacruzensis, Dictyonema pectinatum, and D. galapagoense, here recombined as Cyphellostereum galapagoense. Our analysis is set on a very broad phylogenetic framework, which includes a large number of specimens (N = 826) mainly from Central and South America, and therefore strongly suggests an unusually high level of endemism previously not recognized. This analysis also shows that the closest relatives of half of the basidiolichens now found in Galapagos are from mainland Ecuador, implying that they reached the islands through the shortest route, with all species arriving on the islands through independent colonization events.

1 September 2013 in Fungal Biology
Verified
Journal Article
Closed access
MFManuela Dal Forno
Manuela Dal Forno
JLJames D. Lawrey
James D. Lawrey
MSMasoumeh Sikaroodi
Masoumeh Sikaroodi
SBSmriti Bhattarai
Smriti Bhattarai
PGPatrick M. Gillevet
Patrick M. Gillevet
RLRobert Lücking
Robert Lücking