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Marcelo Pinto Marcelli

Bio: Marcelo Pinto Marcelli is an academic researcher from University of São Paulo. The author has contributed to research in topics: Parmeliaceae & Parmotrema. The author has an hindex of 16, co-authored 84 publications receiving 1279 citations.
Topics: Parmeliaceae, Parmotrema, Punctelia, Lichen, Leptogium


Papers
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Journal ArticleDOI
H. Thorsten Lumbsch1, Teuvo Ahti2, Susanne Altermann3, Guillermo Amo de Paz4, André Aptroot, Ulf Arup, Alejandrina Barcenas Peña5, Paulina A. Bawingan6, Michel Navarro Benatti, Luisa Betancourt, Curtis R. Björk7, Kansri Boonpragob8, Maarten Brand, Frank Bungartz9, Marcela Eugenia da Silva Cáceres, Mehtmet Candan10, José Luis Chaves, Philippe Clerc, Ralph S. Common, Brian J. Coppins11, Ana Crespo4, Manuela Dal-Forno12, Pradeep K. Divakar4, Melizar V. Duya13, John A. Elix14, Arve Elvebakk15, Johnathon D. Fankhauser16, Edith Farkas17, Lidia Itati Ferraro18, Eberhard Fischer19, David J. Galloway20, Ester Gaya21, Mireia Giralt, Trevor Goward22, Martin Grube23, Josef Hafellner23, Jesús E. Hernández M., Maria de los Angeles Herrera Campos5, Klaus Kalb, Ingvar Kärnefelt, Gintaras Kantvilas, Dorothee Killmann19, Paul M. Kirika, Kerry Knudsen24, Harald Komposch, Sergey Y. Kondratyuk, James D. Lawrey12, Armin Mangold, Marcelo Pinto Marcelli, Bruce McCune25, María Inés Messuti26, Andrea Michlig18, Ricardo Miranda González5, Bibiana Moncada, Alifereti Naikatini27, Matthew P. Nelsen28, Dag Olav Øvstedal29, Zdenek Palice30, Zdenek Palice31, Khwanruan Papong32, Sittiporn Parnmen8, Sergio Pérez-Ortega4, Christian Printzen, Víctor J. Rico4, Eimy Rivas Plata33, Javier Robayo, Dania Rosabal34, Ulrike Ruprecht35, Noris Salazar Allen36, Leopoldo G. Sancho4, Luciana Santo de Jesus, Tamires dos Santos Vieira, Matthias Schultz37, Mark R. D. Seaward38, Emmanuël Sérusiaux39, Imke Schmitt40, Harrie J. M. Sipman, Mohammad Sohrabi2, Ulrik Søchting41, Majbrit Zeuthen Søgaard41, Laurens B. Sparrius, Adriano Afonso Spielmann, Toby Spribille23, Jutarat Sutjaritturakan42, Achra Thammathaworn43, Arne Thell, Göran Thor44, Holger Thüs45, Einar Timdal46, Camille Truong, Roman Türk35, Loengrin Umana Tenorio, Dalip K. Upreti47, Pieter P. G. van den Boom, Mercedes Rebuelta4, Mats Wedin, Susan Will-Wolf48, Volkmar Wirth49, Nora Wirtz, Rebecca Yahr11, Kumelachew Yeshitela19, Frauke Ziemmeck9, Tim Wheeler, Robert Lücking1 
Field Museum of Natural History1, American Museum of Natural History2, University of California, Santa Cruz3, Complutense University of Madrid4, National Autonomous University of Mexico5, Saint Louis University6, University of Idaho7, Ramkhamhaeng University8, Charles Darwin Foundation9, Anadolu University10, Royal Botanic Garden Edinburgh11, George Mason University12, Conservation International13, Australian National University14, University of Tromsø15, University of Minnesota16, Hungarian Academy of Sciences17, National University of the Northeast18, University of Koblenz and Landau19, Landcare Research20, University of Barcelona21, University of British Columbia22, University of Graz23, University of California, Riverside24, Oregon University System25, National Scientific and Technical Research Council26, University of the South Pacific27, University of Chicago28, University of Bergen29, Academy of Sciences of the Czech Republic30, Charles University in Prague31, Mahasarakham University32, University of Illinois at Chicago33, Universidad de Oriente34, University of Salzburg35, Smithsonian Tropical Research Institute36, University of Hamburg37, University of Bradford38, University of Liège39, Goethe University Frankfurt40, University of Copenhagen41, King Mongkut's Institute of Technology Ladkrabang42, Khon Kaen University43, Swedish University of Agricultural Sciences44, Natural History Museum45, University of Oslo46, Council of Scientific and Industrial Research47, University of Wisconsin-Madison48, Museum für Naturkunde49
TL;DR: A total of 100 new species of lichenized fungi are described, representing a wide taxonomic and geographic range, and emphasizing the dire need for taxonomic expertise in lichenology.
Abstract: The number of undescribed species of lichenized fungi has been estimated at roughly 10,000. Describing and cataloging these would take the existing number of taxonomists several decades; however, the support for taxonomy is in decline worldwide. In this paper we emphasize the dire need for taxonomic expertise in lichenology. We bring together 103 colleagues from institutions worldwide to describe a total of 100 new species of lichenized fungi, representing a wide taxonomic and geographic range. The newly described species are: Acarospora flavisparsa, A. janae, Aderkomyces thailandicus, Amandinea maritima, Ampliotrema cocosense, Anomomorpha lecanorina, A. tuberculata, Aspicilia mansourii, Bacidina sorediata, Badimia multiseptata, B. vezdana, Biatora epirotica, Buellia sulphurica, Bunodophoron pinnatum, Byssoloma spinulosum, Calopadia cinereopruinosa, C. editae, Caloplaca brownlieae, C. decipioides, C. digitaurea, C. magnussoniana, C. mereschkowskiana, C. yorkensis, Calvitimela uniseptata, Chapsa microspora, C. psoromica, C. rubropulveracea, C. thallotrema, Chiodecton pustuliferum, Cladonia mongkolsukii, Clypeopyrenis porinoides, Coccocarpia delicatula, Coenogonium flammeum, Cresponea ancistrosporelloides, Crocynia microphyllina, Dictyonema hernandezii, D. hirsutum, Diorygma microsporum, D. sticticum, Echinoplaca pernambucensis, E. schizidiifera, Eremithallus marusae, Everniastrum constictovexans, Fellhanera borbonica, Fibrillithecis sprucei, Fissurina astroisidiata, F. nigrolabiata, F. subcomparimuralis, Graphis caribica, G. cerradensis, G. itatiaiensis, G. marusa, Gyalideopsis chicaque, Gyrotrema papillatum, Harpidium gavilaniae, Hypogymnia amplexa, Hypotrachyna guatemalensis, H. indica, H. lueckingii, H. paracitrella, H. paraphyscioides, H. parasinuosa, Icmadophila eucalypti, Krogia microphylla, Lecanora mugambii, L. printzenii, L. xanthoplumosella, Lecidea lygommella, Lecidella greenii, Lempholemma corticola, Lepraria sekikaica, Lobariella sipmanii, Megalospora austropacifica, M. galapagoensis, Menegazzia endocrocea, Myriotrema endoflavescens, Ocellularia albobullata, O. vizcayensis, Ochrolechia insularis, Opegrapha viridipruinosa, Pannaria phyllidiata, Parmelia asiatica, Pertusaria conspersa, Phlyctis psoromica, Placopsis imshaugii, Platismatia wheeleri, Porina huainamdungensis, Ramalina hyrcana, R. stoffersii, Relicina colombiana, Rhizocarpon diploschistidina, Sticta venosa, Sagenidiopsis isidiata, Tapellaria albomarginata, Thelotrema fijiense, Tricharia nigriuncinata, Usnea galapagona, U. pallidocarpa, Verrucaria rhizicola, and Xanthomendoza rosmarieae. In addition, three new combinations are proposed: Fibrillithecis dehiscens, Lobariella botryoides, and Lobariella pallida.

215 citations

Journal ArticleDOI
TL;DR: The Canoparmelia texana epiphytic lichenized fungi was used to monitor atmospheric pollution in the São Paulo metropolitan region and revealed that the accumulation of toxic elements in C. texana may be of use in evaluating the human risk of cardiopulmonary mortality due to prolonged exposure to ambient levels of air pollution.

62 citations

Journal ArticleDOI
TL;DR: Based on an updated phylogeny using the ITS fungal barcoding locus, Cora is 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.
Abstract: 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, Madrinan & Lucking spec. nov., C. applanata Moncada, Soto-Medina & Lucking spec. nov., C. arachnodavidea Moncada, Dal Forno & Lucking spec. nov., C. arborescens Dal Forno, Chaves & Lucking spec. nov., C. arcabucana Moncada, C. Rodriguez & Lucking spec. nov., C. aturucoa Lucking, Moncada & C. Vargas spec. nov., C. auriculeslia Moncada, Yanez-Ayabaca & Lucking spec. nov., C. barbifera Moncada, Patino & Lucking spec. nov., C. boleslia Lucking, 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 & Lucking spec. nov., C. caraana Lucking, Martins & Lucheta spec. nov., C. casasolana Moncada, R.-E. Perez & Lucking spec. nov., C. caucensis Moncada, M. Gut. & Lucking spec. nov., C. celestinoa Moncada, Cabrera-Amaya & Lucking spec. nov., C. comaltepeca Moncada, R.-E. Perez & Herrera-Camp. spec. nov., C. corani Lucking, E. Morales & Dal Forno spec. nov., C. corelleslia Moncada, A. Suarez-Corredor & Lucking spec. nov., C. crispoleslia Moncada, J. Molina & Lucking spec. nov., C. cuzcoensis Holgado, Rivas Plata & Perlmutter spec. nov., C. dalehana Moncada, Madrinan & Lucking spec. nov., C. davibogotana Lucking, Moncada & Coca spec. nov., C. davicrinita Moncada, Madrinan & Lucking spec. nov., C. davidia Moncada, L. Vargas & Lucking spec. nov., C. dewisanti Moncada, A. Suarez-Corredor & Lucking spec. nov., C. dulcis Moncada, R.-E. Perez & Lucking spec. nov., C. elephas Lucking, Moncada & L. Vargas spec. nov., C. fuscodavidiana Lucking, Moncada & L. Vargas spec. nov., C. garagoa Simijaca, Moncada & Lucking spec. nov., C. gigantea Lucking, Moncada & Coca spec. nov., C. gomeziana Dal Forno, Chaves & Lucking spec. nov., C. guajalitensis Lucking, Robayo & Dal Forno spec. nov., C. hafecesweorthensis Moncada, Lucking & R. Pelaez spec. nov., C. haledana Dal Forno, Chaves & Lucking spec. nov., C. hawksworthiana Dal Forno, P. Nelson & Lucking spec. nov., C. hochesuordensis Lucking, E. Morales & Dal Forno spec. nov., C. hymenocarpa Lucking, Chaves & Lawrey spec. nov., C. imi Lucking, Chaves & Lawrey spec. nov., C. itabaiana Dal Forno, Aptroot & M. Caceres spec. nov., C. leslactuca Lucking, Moncada & R. Pelaez spec. nov., C. maxima Wilk, Dal Forno & Lucking spec. nov., C. minutula Lucking, Moncada & Yanez-Ayabaca spec. nov., C. palaeotropica Weerakoon, Aptroot & Lucking spec. nov., C. palustris Dal Forno, Chaves & Lucking spec. nov., C. parabovei Dal Forno, Kukwa & Lucking spec. nov., C. paraciferrii Lucking, Moncada & J.E. Hern. spec. nov., C. paraminor Dal Forno, Chaves & Lucking spec. nov., C. pastorum Moncada, Patino & Lucking spec. nov., C. pichinchensis Paredes, Jonitz & Dal Forno spec. nov., C. pikynasa J.-M. Torres, Moncada & Lucking spec. nov., C. pseudobovei Wilk, Dal Forno & Lucking spec. nov., C. pseudocorani Lucking, E. Morales & Dal Forno spec. nov., C. putumayensis L.J. Arias, Moncada & Lucking spec. nov., C. quillacinga Moncada, F. Ortega & Lucking spec. nov., C. rothesiorum Moncada, Madrinan & Lucking spec. nov., C. rubrosanguinea Nugra, Moncada & Lucking spec. nov., C. santacruzensis Dal Forno, Bungartz & Yanez-Ayabaca, spec. nov., C. schizophylloides Moncada, C. Rodriguez & Lucking spec. nov., C. smaragdina Lucking, Rivas Plata & Chaves spec. nov., C. soredavidia Dal Forno, Marcelli & Lucking spec. nov., C. subdavicrinita Moncada, J. Molina & Lucking spec. nov., C. suturifera Nugra, Besal & Lucking spec. nov., C. terrestris Dal Forno, Chaves & Lucking spec. nov., C. terricoleslia Wilk, Dal Forno & Lucking spec. nov., C. udebeceana Moncada, R. Pelaez & Lucking spec. nov., C. urceolata Moncada, Coca & Lucking spec. nov., C. verjonensis Lucking, Moncada & Dal Forno spec. nov., C. viliewoa Lucking, Chaves & Soto-Medina spec. nov., and C. yukiboa Mercado-Diaz, Moncada & Lucking spec. nov. Furthermore, the taxonomic status of the recently described or recognized species C. arachnoidea, C. aspera, C. ciferrii, and C. reticulifera, is revised.

56 citations

Journal ArticleDOI
TL;DR: It is concluded that knowledge of the Argentinean lichen flora is patchy and depends on the accessibility of the study area and historical factors of each region, rather than on the phytogeographic area considered.
Abstract: This paper presents an assessment of the lichen taxa cited for Argentina, as related to botanical expeditions and in the context of their distribution both in the four vascular flora phytogeographic dominions and in geographic provinces. Three chronological periods are considered: the first, up to the middle of the 20th century, when Grassi published the Catalogue of Argentine Lichens (first catalogue of its kind in Latin America), the second, up to the 1970s and the third, up to the present. The work of Argentine research groups is discussed, including data from bibliographical sources and researchers’ personal communications. The relationship between contributions by local and foreign scientists is discussed. It is concluded that knowledge of the Argentinean lichen flora is patchy and depends on the accessibility of the study area and historical factors of each region, rather than on the phytogeographic area considered.

46 citations


Cited by
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TL;DR: In this paper, the authors quantify how much of the Brazilian Atlantic Forest still remains, and analyze its spatial distribution, and suggest some guidelines for conservation: (i) large mature forest fragments should be a conservation priority; (ii) smaller fragments can be managed in order to maintain functionally linked mosaics; (iii) the matrix surrounding fragments, and (iv) restoration actions should be taken, particularly in certain key areas.

3,199 citations

Journal ArticleDOI
TL;DR: Elton's "The Ecology of Invasions by Animals and Plants" as mentioned in this paper is one of the most cited books on invasion biology, and it provides an accessible, engaging introduction to the most important environmental crises of our time.
Abstract: Much as Rachel Carson's \"Silent Spring\" was a call to action against the pesticides that were devastating bird populations, Charles S. Elton's classic \"The Ecology of Invasions by Animals and Plants\" sounded an early warning about an environmental catastrophe that has become all too familiar today-the invasion of nonnative species. From kudzu to zebra mussels to Asian long-horned beetles, nonnative species are colonizing new habitats around the world at an alarming rate thanks to accidental and intentional human intervention. One of the leading causes of extinctions of native animals and plants, invasive species also wreak severe economic havoc, causing $79 billion worth of damage in the United States alone. Elton explains the devastating effects that invasive species can have on local ecosystems in clear, concise language and with numerous examples. The first book on invasion biology, and still the most cited, Elton's masterpiece provides an accessible, engaging introduction to one of the most important environmental crises of our time. Charles S. Elton was one of the founders of ecology, who also established and led Oxford University's Bureau of Animal Population. His work has influenced generations of ecologists and zoologists, and his publications remain central to the literature in modern biology. \"History has caught up with Charles Elton's foresight, and \"The Ecology of Invasions\" can now be seen as one of the central scientific books of our century.\"-David Quammen, from the Foreword to \"Killer Algae: The True Tale of a Biological Invasion\

1,321 citations

Journal ArticleDOI
TL;DR: New evidence is examined from various sources to derive an updated estimate of global fungal diversity, concluding that the commonly cited estimate of 1.5 million species is conservative and that the actual range is properly estimated at 2.2 to 3.8 million.
Abstract: The question of how many species of Fungi there are has occasioned much speculation, with figures mostly posited from around half a million to 10 million, and in one extreme case even a sizable portion of the spectacular number of 1 trillion. Here we examine new evidence from various sources to derive an updated estimate of global fungal diversity. The rates and patterns in the description of new species from the 1750s show no sign of approaching an asymptote and even accelerated in the 2010s after the advent of molecular approaches to species delimitation. Species recognition studies of (semi-)cryptic species hidden in morpho-species complexes suggest a weighted average ratio of about an order of magnitude for the number of species recognized after and before such studies. New evidence also comes from extrapolations of plant:fungus ratios, with information now being generated from environmental sequence studies, including comparisons of molecular and fieldwork data from the same sites. We further draw attention to undescribed species awaiting discovery in biodiversity hot spots in the tropics, little-explored habitats (such as lichen-inhabiting fungi), and material in collections awaiting study. We conclude that the commonly cited estimate of 1.5 million species is conservative and that the actual range is properly estimated at 2.2 to 3.8 million. With 120,000 currently accepted species, it appears that at best just 8%, and in the worst case scenario just 3%, are named so far. Improved estimates hinge particularly on reliable statistical and phylogenetic approaches to analyze the rapidly increasing amount of environmental sequence data.

759 citations

Journal ArticleDOI
Guo Jie Li1, Kevin D. Hyde2, Kevin D. Hyde3, Kevin D. Hyde4  +161 moreInstitutions (45)
TL;DR: 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.
Abstract: Notes on 113 fungal taxa are compiled in this paper, including 11 new genera, 89 new species, one new subspecies, three new combinations and seven reference specimens. A wide geographic and taxonomic range of fungal taxa are detailed. In the Ascomycota the new genera Angustospora (Testudinaceae), Camporesia (Xylariaceae), Clematidis, Crassiparies (Pleosporales genera incertae sedis), Farasanispora, Longiostiolum (Pleosporales genera incertae sedis), Multilocularia (Parabambusicolaceae), Neophaeocryptopus (Dothideaceae), Parameliola (Pleosporales genera incertae sedis), and Towyspora (Lentitheciaceae) are introduced. Newly introduced species are Angustospora nilensis, Aniptodera aquibella, Annulohypoxylon albidiscum, Astrocystis thailandica, Camporesia sambuci, Clematidis italica, Colletotrichum menispermi, C. quinquefoliae, Comoclathris pimpinellae, Crassiparies quadrisporus, Cytospora salicicola, Diatrype thailandica, Dothiorella rhamni, Durotheca macrostroma, Farasanispora avicenniae, Halorosellinia rhizophorae, Humicola koreana, Hypoxylon lilloi, Kirschsteiniothelia tectonae, Lindgomyces okinawaensis, Longiostiolum tectonae, Lophiostoma pseudoarmatisporum, Moelleriella phukhiaoensis, M. pongdueatensis, Mucoharknessia anthoxanthi, Multilocularia bambusae, Multiseptospora thysanolaenae, Neophaeocryptopus cytisi, Ocellularia arachchigei, O. ratnapurensis, Ochronectria thailandica, Ophiocordyceps karstii, Parameliola acaciae, P. dimocarpi, Parastagonospora cumpignensis, Pseudodidymosphaeria phlei, Polyplosphaeria thailandica, Pseudolachnella brevifusiformis, Psiloglonium macrosporum, Rhabdodiscus albodenticulatus, Rosellinia chiangmaiensis, Saccothecium rubi, Seimatosporium pseudocornii, S. pseudorosae, Sigarispora ononidis and Towyspora aestuari. New combinations are provided for Eutiarosporella dactylidis (sexual morph described and illustrated) and Pseudocamarosporium pini. Descriptions, illustrations and / or reference specimens are designated for Aposphaeria corallinolutea, Cryptovalsa ampelina, Dothiorella vidmadera, Ophiocordyceps formosana, Petrakia echinata, Phragmoporthe conformis and Pseudocamarosporium pini. The new species of Basidiomycota are Agaricus coccyginus, A. luteofibrillosus, Amanita atrobrunnea, A. digitosa, A. gleocystidiosa, A. pyriformis, A. strobilipes, Bondarzewia tibetica, Cortinarius albosericeus, C. badioflavidus, C. dentigratus, C. duboisensis, C. fragrantissimus, C. roseobasilis, C. vinaceobrunneus, C. vinaceogrisescens, C. wahkiacus, Cyanoboletus hymenoglutinosus, Fomitiporia atlantica, F. subtilissima, Ganoderma wuzhishanensis, Inonotus shoreicola, Lactifluus armeniacus, L. ramipilosus, Leccinum indoaurantiacum, Musumecia alpina, M. sardoa, Russula amethystina subp. tengii and R. wangii are introduced. Descriptions, illustrations, notes and / or reference specimens are designated for Clarkeinda trachodes, Dentocorticium ussuricum, Galzinia longibasidia, Lentinus stuppeus and Leptocorticium tenellum. The other new genera, species new combinations are Anaeromyces robustus, Neocallimastix californiae and Piromyces finnis from Neocallimastigomycota, Phytophthora estuarina, P. rhizophorae, Salispina, S. intermedia, S. lobata and S. spinosa from Oomycota, and Absidia stercoraria, Gongronella orasabula, Mortierella calciphila, Mucor caatinguensis, M. koreanus, M. merdicola and Rhizopus koreanus in Zygomycota.

488 citations

Journal ArticleDOI
TL;DR: This paper examined the geographic distribution of biological diversity in the Atlantic Forest of South America, synthesized the most conspicuous forest biodiversity responses to human disturbances, and proposed further conservation initiatives for this biota, and offer a range of general insights into the prospects of forest species persistence in human-modified tropical forest landscapes worldwide.

380 citations