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A dynamic online documentation of Italian ascomycetes with hosts and substrates: www.italianmicrofungi.org

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Early taxonomic studies of ascomycetous microfungi were conducted based on morphological observations. With the advent and advancement of DNA based molecular studies over the last few decades, species, genera, families and orders of Ascomycota have been subjected to rapid taxonomic changes. In the last eight years, we have introduced many novel fungal taxa with numerous new host and country records of ascomycetous microfungi from Italy. Dothideomycetes and Sordariomycetes are the major classes that we have investigated. These fungal species were collected from more than 300 host species in terrestrial habitats of different provinces in Italy. The hosts include shrubs, trees and grasses with the substrates differentiated as branches, stems and leaves. For these taxa, identification and classification were confirmed with comprehensive descriptions, colour illustrations and multi-gene phylogenetic analyses. These studies are scattered in different scientific journals. The online documentation at www.italianmicrofungi.org is a database for arranging all the published data together with novel updates of present and upcoming studies. Notes for species, genera and up-to-date records of Italian ascomycetes with accounts on different hosts and substrates are described here. This website provides a user-friendly and easily accessible framework to extract more information.
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Submitted 9 July 2020, Accepted 21 December 2020, Published 21 January 2021
Corresponding Author: Kevin D. Hydee-mail kdhyde3@gmail.com 1
A dynamic online documentation of Italian ascomycetes with hosts
and substrates: www.italianmicrofungi.org
Wijesinghe SN1,2, Camporesi E3, Wanasinghe DN4,9,10, Maharachchikumbura
SSN5, Senanayake IC6,8, Phookamsak R4,9,10,11, Hongsanan S6, Tibpromma S4,9,10,
Thambugala KM7, Luangharn T1, McKenzie EHC12 and Hyde KD1,4,8*
1Center of Excellence in Fungal Research, Mae Fah Luang University, Chiang Rai 57100, Thailand
2School of Science, Mae Fah Luang University, Chiang Rai 57100, Thailand
3A.M.B. Gruppo Micologico Forlivese Antonio Cicognani, Via Roma 18, Forlì, Italy
4CAS Key Laboratory for Plant Biodiversity and Biogeography of East Asia, Kunming Institute of Botany, Chinese
Academy of Sciences, Kunming 650201, Yunnan, Peoples Republic of China
5School of Life Science and Technology, University of Electronic Science and Technology of China, Chengdu, 611731,
Peoples Republic of China
6Guangdong Provincial Key Laboratory for Plant Epigenetics, Shenzhen Key Laboratory of Microbial Genetic
Engineering, College of Life Science and Oceanography, Shenzhen University, Shenzhen 518060, Peoples Republic of
China
7Genetics and Molecular Biology Unit, Faculty of Applied Sciences, University of Sri Jayewardenepura, Gangodawila,
Nugegoda, Sri Lanka
8Innovative Institute of Plant Health, Zhongkai University of Agriculture and Engineering, Haizhu District, Guangzhou
510225, Peoples Republic of China
9East and Central Asia Regional Office, World Agroforestry Centre (ICRAF), Kunming 650201, Yunnan, Peoples
Republic of China
10Honghe Center for Mountain Futures, Kunming Institute of Botany, Chinese Academy of Sciences, Honghe County,
Yunnan, Peoples Republic of China
11Research Center of Microbial Diversity and Sustainable Utilization, Faculty of Sciences, Chiang Mai University,
Chiang Mai 50200, Thailand
12Manaaki Whenua-Landcare Research, Private Bag 92170, Auckland Mail Centre, Auckland 1142, New Zealand
Wijesinghe SN, Camporesi E, Wanasinghe DN, Maharachchikumbura SSN, Senanayake IC,
Phookamsak R, Hongsanan S, Tibpromma S, Thambugala KM, Luangharn T, McKenzie EHC and
Hyde KD 2021 A dynamic online documentation of Italian ascomycetes with hosts and
substrates: www.italianmicrofungi.org. Asian Journal of Mycology 4(1), 1018, Doi
10.5943/ajom/4/1/2
Abstract
Early taxonomic studies of ascomycetous microfungi were conducted based on
morphological observations. With the advent and advancement of DNA based molecular studies
over the last few decades, species, genera, families and orders of Ascomycota have been subjected
to rapid taxonomic changes. In the last eight years, we have introduced many novel fungal taxa
with numerous new host and country records of ascomycetous microfungi from Italy.
Dothideomycetes and Sordariomycetes are the major classes that we have investigated. These
fungal species were collected from more than 300 host species in terrestrial habitats of different
provinces in Italy. The hosts include shrubs, trees and grasses with the substrates differentiated as
branches, stems and leaves. For these taxa, identification and classification were confirmed with
comprehensive descriptions, colour illustrations and multi-gene phylogenetic analyses. These
studies are scattered in different scientific journals. The online documentation at
Asian Journal of Mycology 4(1): 1018 (2021) ISSN 2651-1339
www.asianjournalofmycology.org Article
Doi 10.5943/ajom/4/1/2
2
www.italianmicrofungi.org is a database for arranging all the published data together with novel
updates of present and upcoming studies. Notes for species, genera and up-to-date records of Italian
ascomycetes with accounts on different hosts and substrates are described here. This website
provides a user-friendly and easily accessible framework to extract more information.
Keywords Classification Dothideomycetes Phylogeny Sordariomycetes Taxonomy
Webpage
Introduction
Fungi are ubiquitous and a highly diverse group of eukaryotes (Hyde et al. 2018, Sun et al.
2019). Their lifestyles vary as biotrophic, endophytic, epiphytic, hemibiotrophic, saprobic or
fungicolous (Hyde et al. 2018, Sun et al. 2019, Tennakoon et al. 2020). Over the last 300 years,
fungal identification, classification, and speculation on the relationships among taxa were based on
phenotypic characters. These phenotypic observations have been used as major tools of fungal
researchers and were recorded with descriptions and line drawings (Hyde et al. 2011, Jayasiri et al.
2015, Tekpinar & Kalmer 2019, Tennakoon et al. 2020). However, morphology may not always
reflect phylogenetic relationships (Judd et al. 2002). Identification of species based on morphology
is challenging and highly subjective, especially among species complexes, non-sporulating fungi
and cryptic species (Jeewon et al. 2002, Promputtha et al. 2005, 2007, Jayasiri et al. 2015). The
initial investigations of phenotypic approaches, as well as chemical, ecological, molecular and
physiological analyses, are very important in fungal taxonomy (Manawasinghe et al. 2019). The
project, Assembling the Fungal Tree of Life (AFToL), provided molecular data for most of the
orders and families of Ascomycota, and this was the start of the golden era of mycology (James et
al. 2006, Hyde et al. 2020a). Morphology was linked to analyze the results from advanced
molecular techniques, and DNA based phylogeny was developed as informative tools with better
taxonomic resolution (Senanayake et al. 2017a, Hongsanan et al. 2018, Wanasinghe et al. 2018,
Tennakoon et al. 2020). This combined taxonomic approach has led to the resolution of numerous
taxonomic issues and has provided more reliable classification than traditional morphology-based
tools (Jayasiri et al. 2015).
Earlier treatments in Italian mycology dealt with macrofungi (Venturella 1991). Alfonso
Ciccarelli (15321585) completed the first mycological monograph for macrofungi in Italy based
on morphological and organoleptic aspects of truffles (Ciccarelli 1564). However, Italian
microfungal publications were concerned with only a few taxa (Venturella 1991). Giuseppe de
Notaris (18051877), Vincenzo de Cesati (18061883) and Pier Andrea Saccardo (18451920)
were significant early contributors to Italian, as well as world mycology (Onofri et al. 1999,
Phukhamsakda et al. 2020). Pampaloni (1902) reported the fossil records of Italian ascomycetes
related to the Miocene epoch. Saccardo (1882) provided detailed documentation for mycology and
a rapid increase in microfungal studies occurred between 19311990 (Venturella 1991). A checklist
of Sicilian fungi (Southern Italy) including hosts and substrates was published by Venturella
(1991), and it is a very important resource for understanding Italian fungal diversity and ecology.
Zucconi et al. (1997) studied the dematiaceous hyphomycetes microfungal communities in
Mediterranean evergreen forests in central Italy. Venturella et al. (2011) reported the estimated
number of regional ascomycetes and basidiomycetes up to 2010. The history of Italian mycology
and the valuable contributions of great mycologists are reported by Siniscalco et al. (2013).
Ascomycota is the largest phylum, comprising Dothideomycetes and Sordariomycetes as
major classes in the subphylum, Pezizomycotina (Hyde et al. 2013, 2020a, Maharachchikumbura et
al. 2015, 2016, Wijayawardene et al. 2018, 2020, Hongsanan et al. 2020). PhD researchers and
expert mycologists in the Center of Excellence in Fungal Research (CEFR) group have studied
most of the Italian ascomycetes collected by Erio Camporesi who has promoted mycological
studies as a prodigious amateur mycologist (Phukhamsakda et al. 2020). Currently, several PhD
students at CEFR are studying fresh specimens from Erio Camporesi with amazing discoveries of
novel taxa as well as novel host and geographical records of ascomycetes. These CEFR studies are
3
published regularly in different scientific journals. “Asian Journal of Mycology notes, Fungal
diversity notes and Mycosphere notesare key journal series providing more information of
worldwide fungi and include many Italian ascomycetes (Ariyawansa et al. 2015, Wijayawardene et
al. 2016, Hyde et al. 2017, 2019, 2020a, b, c, Senanayake et al. 2017b, Jayawardena et al. 2018,
Wanasinghe et al. 2018, Phookamsak et al. 2019). Preserving scientific data through the
documentation by recording fungal morphology, taxonomy and ecological information is a valuable
process in mycology (Lange 2010). Mycologists have a responsibility to popularize fungal
information, by inspiring and spreading informative outreach materials, and providing easily
accessible websites, and openly accessed databases (Lange 2010). A strong foundation for applied
biological fields such as ecology, pathology and industrial can be provided through spreading
primary fungal taxonomic data.
Why Italian microfungi are very important?
Early studies of Italian microfungi were based on morphological observations, as was the
case worldwide. Several mycologists in Italy contributed immensely to fungal systematics by
extensive collections of fungal specimens. Notable among these were the collections and early
studies by P. A. Saccardo. Italian fungal specimens are significant to study as among them are new
orders, families, genera and species as well as new hosts and geographic reports. Recollecting
fungal specimens can serve as epitypes and authentic herbarium materials of extant species with
sequence data. The host specificity and life mode details can be updated when dealing with
recollected specimens from different environments and host plants.
The need for Italian microfungi database
There is a massive collection of publications for Italian microfungi by the CEFR group.
These documentations can be categorized as providing novel taxa, new host records and new
geographical records from Italian sites. These publications comprise species descriptions,
illustrations, and molecular phylogeny, which provides a comprehensive analysis of species
delineation. However, it largely remains to reconstruct the accurate taxonomic placements for all
taxa, especially for earliest studied taxa with their DNA sequence data. In our new website, we deal
with the information of previously published Italian ascomycetes and will provide continuous
updates from novel studies that are currently being processed by the CEFR group. The objectives of
this website are to gather all information into one comprehensive source and to make it readily
available to mycologists worldwide. This study provides up-to-date accounts of Italian ascomycetes
on different hosts and substrates with recent taxonomic changes. In addition, we also provide notes
on genera and species reported from Italy.
Importance of gathering morphological and ecological data into a single tool
The preference of modern researchers is increasingly to refer to databases rather than books
and other publications to gather the scattered knowledge. A database is technically easy to handle
and much less time-consuming. Therefore, gathering morphological and ecological data into a
single tool is a very flexible and time-saving method for researchers. Index Fungorum
(www.indexfungorum.org), MycoBank (www.mycobank.org), Facesoffungi
(www.facesoffungi.org), Sordariomycetes (www.sordariomycetes.org), Dothideomycetes
(www.dothideomycetes.org) and Coelomycetes (www.coelomycetes.org) are commonly used
websites in studies of ascomycetes.
Italian microfungi website
In the Italian microfungi website, ascomycetous species associated with over 300 hosts from
different regions in Italy have been identified. The substrates are reported mainly as branches (from
shrubs and trees), stems (from herbaceous hosts and grasses) and rarely leaves (from shrubs, trees
and grasses). These specimens are mainly from the provinces of Forlì-Cesena (in the region of
Emilia-Romagna) and Arezzo (in the region of Tuscany) with fewer collections from the provinces
4
of Bologna and Ravenna (in Emilia-Romagna), Firenze (in Tuscany), Pesaro-Urbino (in Marche),
Trento (in Trentino-Alto Adige) and Udine (Friuli-Venezia Giulia). This is an informative and user-
friendly platform to provide in-depth knowledge of Italian ascomycetes and related host species.
The host specificity and the life modes of Italian ascomycetes are evaluated. In the pursuit of
discovering more fungi from Italy, this study is extending to investigate the taxonomy and
phylogeny of microfungal taxa. In addition, the other websites from the CEFR group;
Dothideomycetes (www.dothideomycetes.org; Pem et al. 2019), Sordariomycetes
(www.sordariomycetes.org; Bundhun et al. 2020) and Coelomycetes (www.coelomycetes.org;
Wijayawardene et al. 2016, Li et al. 2020) are linked to this new website for extracting relevant
information of Italian ascomycetes.
Construction
Italian ascomycetes, which were identified and published by the CEFR group, are listed on
the website together with their hosts and substrates. Species, which are currently being studied, will
be regularly entered. For each entry of identified species, Index Fungorum, Facesoffungi,
MycoBank and/or ex-type culture collection, dry culture collection, herbaria numbers and available
GenBank numbers for sequence data are provided. Updated information is periodically inserted
based on both previous and novel studies. Mycological experts who studied large numbers of
Italian ascomycetes during the past eight years have been assigned as curators to share their
knowledge and suggestions (Table 1).
Table 1 List of curators for Italian microfungi webpage.
Position
Name
Email address
Head curator
Kevin Hyde
kdhyde3@gmail.com
Expert curator
Erio Camporesi
eriocamporesi@libero.it
Managing curator
Subodini Wijesinghe
nuwanthika.was90@gmail.com
Curators
Dhanushka Wanasinghe
dnadeeshan@gmail.com
Indunil Senanayake
indunilchinthani@gmail.com
Kasun Thambugala
kasunthambugala@gmail.com
Rungtiwa Phooksamsak
jomjam.rp2@gmail.com
Sinang Hongsanan
sinang333@gmail.com
Sajeewa Maharachchikumbura
sajeewa83@yahoo.com
Saowaluck Tibpromma
saowaluckfai@gmail.com
Database interface and visualization
The Italian microfungi website is functional, easy to access and navigate for searching. The
overview of the homepage provides a comprehensive understanding of the website at a glance.
There are several navigation bars, searching options and some informative details are visualized on
the homepage (Figs. 1, 2).
Details of main headings
Home The homepage provides a detailed account of our entire project (Figs. 1, 2). When the
user opens the webpage, the objectives are envisioned at the left top (Fig. 1a). The main
headings are described as Home, Host/Substrate, Archives, Curators, History, References,
News and Contact (Fig. 1b). Below the header bar, a search box is included where information
on a specific fungal order, family, genus or species can be searched by entering the name (Fig.
1c). Recent news, genera and species which are updated (Fig. 1d) can be seen at the right side
of the interface. The user can easily cite the webpage using the citation at the front (Fig. 1e).
The contact details (Fig. 2a), publisher and copyright details are provided at the bottom (Fig.
2b).
Host/Substrate This gives the records of host occurrences on which fungal species are
collected. We follow the International Plant Names Index (IPNI) for host identification. The
search option is provided for easy searching of the hosts, based on user requirements (Fig. 3).
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Archives Through this heading, the user can find the taxonomic classification of related taxa
at order, family, genus and species level (Fig. 4). When the user opens the Archives interface,
the list of orders related to Italian fungi is visualized. By clicking on relevant order, the link will
navigate to Read more about the orderor related family list of the order. Inside families, the
list of associated genera and species are available.
Curators Photographs and contact details of curators are provided (Fig. 5, Table 1).
History An account of Italian mycological history, ascomycetes, host list and collecting
provinces are provided (Fig. 6).
References A list of references used in the entries, history and other information related to the
Italian ascomycetes are provided under this heading.
News The key events, new findings and important information regarding Italian microfungi
are included here.
Contact Users can provide their comments and suggestions on this webpage.
Fig. 1 Homepage view of Italian microfungi webpage. a Objectives of the webpage. b Headers. c
Search box. d Recently updated news, recent genera and species. e Citation of the webpage.
Fig. 2Bottom view of the homepage. a Contact details. b Publisher and copyright information.
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Fig. 3Host/substrate header of the webpage. a Find next. b Find previous. c Back to top.
Fig. 4Archives header of the webpage.
Fig. 5Curators header of the webpage.
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Fig. 6History header of the webpage.
Acknowledgements
S.N. Wijesinghe offers her profound gratitude to the Mushroom Research Foundation (MRF),
Thailand for financial support and Mae Fah Luang University. Further, S.N. Wijesinghe would like
to thank Saranyaphat Boonmee for her precious assistance to continue this project. S. Tibpromma
would like to thank the International Postdoctoral Exchange Fellowship Program (number
Y9180822S1), CAS Presidents International Fellowship Initiative (PIFI) (number 2020PC0009),
China Postdoctoral Science Foundation and the Yunnan Human Resources, and Social Security
Department Foundation for funding her postdoctoral research. R. Phookamsak thanks CAS
Presidents International Fellowship Initiative (PIFI) for young staff (Grant No. Y9215811Q1), the
National Science Foundation of China (NSFC) project code 31850410489 (Grant No. Y81I982211)
and Chiang Mai University for their partial support of this research work. S. Hongsanan thanks
National Natural Science Foundation of China for supporting the project Biodiversity, Taxonomy,
Phylogeny, Evolution and Phytogeography of Phytopathogens in Dothideomycetes from Southern
China (Grant No. 31950410548). D.N. Wanasinghe would like to thank CAS Presidents
International Fellowship Initiative (PIFI) for funding his postdoctoral research (number
2019PC0008) and the 64th batch of China Postdoctoral Science Foundation (Grant No.
Y913083271). K.D. Hyde would like to thank the Thailand Research Fund (“Impact of climate
change on fungal diversity and biogeography in the Greater Mekong Sub-region RDG6130001”).
References
Ariyawansa HA, Hyde KD, Jayasiri SC, Buyck B et al. 2015 Fungal diversity notes 111252:
taxonomic and phylogenetic contributions to fungal taxa. Fungal Diversity 75, 27274.
Bundhun D, Maharachchikumbura SSN, Jeewon R, Senanayake IC et al. 2020
https://sordariomycetes.org/, a platform for the identification, ranking. Asian Journal of
Mycology 3, 1321.
Ciccarelli A. 1564 Opusculum de Tuberibus. Pavia.
Hongsanan S, Jeewon R, Purahong W, Xie N et al. 2018 Can we use environmental DNA as
holotypes? Fungal Diversity 92, 130
Hongsanan S, Hyde KD, Phookamsak R, Wanasinghe DN et al. 2020 Refined families of
Dothideomycetidae and Pleosporomycetidae. Mycosphere 11, 15532107.
Hyde KD, McKenzie EHC, Koko TW. 2011 Towards incorporating anamorphic fungi in a natural
classification checklist and notes for 2010. Mycosphere 2, 188.
8
Hyde KD, Jones EBG, Liu JK, Ariyawansa HA et al. 2013 Families of Dothideomycetes. Fungal
Diversity 63, 1313.
Hyde KD, Norphanphoun C, Abreu VP, Bazzicalupo A et al. 2017 Fungal diversity notes 603
708: taxonomic and phylogenetic notes on genera and species. Fungal Diversity 87, 1235.
Hyde KD, Al-Hatmi AM, Andersen B, Boekhout T et al. 2018 The worlds ten most feared fungi.
Fungal Diversity 93, 161194.
Hyde KD, Tennakoon DS, Jeewon R, Bhat DJ et al. 2019 Fungal diversity notes 10361150:
taxonomic and phylogenetic contributions on genera and species of fungal taxa. Fungal
Diversity 96, 1242.
Hyde KD, Norphanphoun C, Maharachchikumbura SSN, Bhat DJ et al. 2020a Refined families of
Sordariomycetes. Mycosphere 11, 3051059.
Hyde KD, Dong Y, Phookamsak R, Jeewon R et al. 2020b Fungal diversity notes 11511276:
taxonomic and phylogenetic contributions on genera and species of fungal taxa. Fungal
Diversity 100, 5277.
Hyde KD, de Silva NI, Jeewon R, Bhat DJ et al. 2020c AJOM new records and collections of
fungi: 1100. Asian Journal of Mycology 3, 22294.
James TY, Kauff F, Schoch CL, Matheny PB et al. 2006 Reconstructing the early evolution of
fungi using a six-gene phylogeny. Nature 443, 818822.
Jayasiri SC, Hyde KD, Ariyawansa HA, Bhat DJ et al. 2015 The Faces of Fungi database: fungal
names linked with morphology, phylogeny and human impacts. Fungal Diversity 74, 318.
Jayawardena RS, Hyde KD, Chethana KWT, Daranagama DA et al. 2018 Mycosphere notes
102168: Saprotrophic fungi on Vitis in China, Italy, Russia and Thailand. Mycosphere 9, 1
114.
Jeewon R, Liew ECY, Hyde KD. 2002 Phylogenetic relationships of Pestalotiopsis and allied
genera inferred from ribosomal DNA sequences and morphological characters. Molecular
Phylogenetics and Evolution 25, 378392.
Judd WS, Campbell CS, Kellogg EA, Stevens PF, Donoghue MJ. 2002 Plant systematics: a
phylogenetic approach, vol 2. Sinauer Associates, Sunderland, pp 139.
Lange L. 2010 The importance of fungi for a more sustainable future on our planet. Fungal
Biology Reviews 24, 9092.
Li WJ, McKenzie EHC, Liu JK, Bhat DJ et al. 2020 Taxonomy and phylogeny of hyaline-spored
coelomycetes. Fungal Diversity 100, 279801.
Maharachchikumbura SSN, Hyde KD, Jones EBG, McKenzie EHC et al. 2015 Towards a natural
classification and backbone tree for Sordariomycetes. Fungal Diversity 72, 199301.
Maharachchikumbura SSN, Hyde KD, Jones EBG, McKenzie EHC et al. 2016 Families of
Sordariomycetes. Fungal Diversity 79, 1317.
Manawasinghe IS, Dissanayake AJ, Li X, Liu M et al. 2019 High genetic diversity and species
complexity of Diaporthe associated with grapevine dieback in China. Frontiers in
Microbiology 10, 1936.
Onofri S, Graniti A, Zucconi L. 1999 Italians in the History of Mycology. Proceedings of a
Symposium held in the Archivio Centrale dello Stato. Rome, 45 October, 1995. Mycotaxon
163 pp.
Pampaloni L. 1902 I resti organici nel Disodile di Melilli in Sicilia. Palaeontographia Italica,
Memorie di Paleontologia 8, 121130.
Pem D, Hongsanan S, Doilom M, Tibpromma S et al. 2019 https://www.Dothideomycetes.org: an
online taxonomic resource for the classification, identification, and nomenclature of
Dothideomycetes. Asian Journal of Mycology 2, 287297.
Phookamsak R, Hyde KD, Jeewon R, Bhat DJ et al. 2019 Fungal diversity notes 9291035:
taxonomic and phylogenetic contributions on genera and species of fungi. Fungal Diversity
95, 1273.
Phukhamsakda C, Wijayawardene NN, Ariyawansa HA, Senanayake IC et al. 2020 The
contributions of Erio Camporesi. Fungal Diversity 100, 13.
9
Promputtha I, Jeewon R, Lumyong S, McKenzie EHC et al. 2005 Ribosomal DNA fingerprinting
in the identification of non-sporulating endophytes from Magnolia liliifera (Magnoliaceae).
Fungal Diversity 20, 167186.
Promputtha I, Lumyong S, Vijaykrishna D, McKenzie EHC et al. 2007 A phylogenetic evaluation
of whether endophytes become saprotrophs at host senescence. Microbial Ecology 53, 579
590.
Saccardo PA. 1882 Michelia: commentarium mycologicum fungos in primas italicos illustrans
(Vol. 2). Typis Seminarii.
Senanayake IC, Crous PW, Groenewald JZ, Maharachchikumbura SSN. 2017a Families of
Diaporthales based on morphological and phylogenetic evidence. Studies in Mycology 86,
217296.
Senanayake IC, Maharachchikumbura SSN, Jeewon R, Promputtha I et al. 2017b
Morphophylogenetic study of Sydowiellaceae reveals several new genera. Mycosphere 8,
172217.
Siniscalco C, Doveri F, Bellato G, Campana L et al. 2013 History of Italian mycology and first
contribution to the correct nomenclature of fungi. ISPRA, Handbooks and Guidelines, Rome.
Sun JZ, Liu XZ, McKenzie EHC, Jeewon R et al. 2019 Fungicolous fungi: terminology,
diversity, distribution, evolution, and species checklist. Fungal Diversity 95, 337430.
Tekpinar AD, Kalmer A. 2019 Utility of various molecular markers in fungal identification and
phylogeny. Nova Hedwigia 109, 187224.
Tennakoon DS, Kuo CH, Hyde KD. 2020 Multi-locus phylogeny reveals Phaeodothis mori sp.
nov. (Didymosphaeriaceae, Pleosporales) from dead leaves of Morus australis. Phytotaxa
428, 241254.
Venturella G. 1991 A checklist of Sicilian fungi. Bocconea 2, 5221.
Venturella G, Altobelli E, Bernicchia A, Di Piazza S et al. 2011 Fungal biodiversity and in situ
conservation in Italy. Plant Biosystems-An International Journal Dealing with all Aspects of
Plant Biology 145, 950957.
Wanasinghe DN, Phukhamsakda C, Hyde KD, Jeewon R et al. 2018 Fungal diversity notes 709
839: taxonomic and phylogenetic contributions to fungal taxa with an emphasis on fungi on
Rosaceae. Fungal Diversity 89, 1236.
Wijayawardene NN, Hyde KD, Wanasinghe DN, Papizadeh M et al. 2016 Taxonomy and
phylogeny of dematiaceous coelomycetes. Fungal Diversity 77, 1316.
Wijayawardene NN, Hyde KD, Lumbsch HT, Liu JK et al. 2018 Outline of Ascomycota: 2017.
Fungal Diversity 88, 167263.
Wijayawardene NN, Hyde KD, Al-Ani LKT, Tedersoo L et al. 2020 Outline of Fungi and
fungus-like taxa. Mycosphere 11, 10601456.
Zucconi L, Facchin M, Perini C 1997 Microfungal communities in Mediterranean evergreen
forests of central Italy. Bocconea 5, 825831.
... Botryosphaeriaceae can also infect native hosts, and then move to other introduced hosts in the same region (Pavlic et al., 2007;Luo et al., 2022). Botryosphaeriaceae are responsible for cankers on host trunks, branches and twigs, dieback and shoot blight, bark cracking, wood discolouration, stemend rots and fruit rots (Carlucci et al., 2015; Aiello et al., 2022Bertetti et al., 2013Carlucci et al., 2013Dardani et al., 2023De Corato et al., 2007Dell'Olmo et al., 2023Dissanayake et al., 2017Fiorenza et al., 2022Garibaldi et al., 2012Grasso and Granata, 2010Gusella et al., 2021Lazzizera et al., 2008bLi et al., 2020Linaldeddu et al., 2009, 2015aMarinelli et al., 2012Martino et al., 2023Moricca et al., 2008Piskur et al., 2011Raimondo et al., 2019Scala et al., 2019Schlegel et al., 2018Spagnolo et al., 2011Turco et al., 2006Wijesinghe et al., 2021Zimowska et al., 2020 Alves et al., 2014Ariyawansa et al., 2015Carlucci et al., 2013Dardani et al., 2023Dissanayake et al., 2017Giambra et al., 2016Lazzizera et al., 2008aLinaldeddu et al., 2006b, 2015a, 2016cLorenzini and Zapparoli, 2018Luchi et al., 2014Martino et al., 2023Mondello et al., 2013Quaglia et al., 2014Raimondo et al., 2019Spagnolo et al., 2011Wijayawardene et al., 2016 (Continued) Aiello et al., 2020Alberti et al., 2018Aloi et al., 2021Bezerra et al., 2021Carlucci et al., 2013Dardani et al., 2023Deidda et al., 2016Dissanayake et al., 2017Faedda et al., 2018Fiorenza et al., 2022Garibaldi et al., 2011Giambra et al., 2016Guarnaccia et al., 2016Gusella et al., 2020a, 2023a, 2023bIsmail et al., 2013Linaldeddu et al., 2007, 2015aLuchi et al., 2014Manca et al., 2020Mang et al., 2022Mondello et al., 2013Moricca et al., 2012Polizzi et al., 2023Raimondo et al., 2019Riccioni et al., 2017Seddaiu et al., 2021Sidoti, 2016Spagnolo et al., 2011 al., 2020, 2022; Gusella et al., 2020aGusella et al., , 2020bGusella et al., , 2021Gusella et al., , 2022Linaldeddu et al., 2020a;Bezerra et al., 2021;Fiorenza et al., , 2023, and these infections are often caused by multiple pathogen genera that may play different roles in infection processes of host plants. ...
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Many fungi belonging to Botryosphaeriaceae are well-known as causal agents of diseases in economically and ecologically important agricultural crops and forest trees. In Italy, the high diffusion of Botryosphaeriaceae infections observed over the last decade, has shown the importance of this group of fungi, which are becoming limiting factors for plant production in agricultural systems, nurseries and natural and urban landscapes. Global warming and stress factors such as occasional extreme climatic events can affect the susceptibility of host plants, as well as fungus behaviour, increasing the risk of future infections. Available reports of Botryosphaeriaceae in Italy have been examined, focusing on wood and fruit pathogens, resulting in a list of ten genera and 57 species. Diplodia is the most widespread genus in Italy with 76 records on 44 hosts, while at species level, Neofusicoccum parvum, Botryosphaeria dothidea and Diplodia seriata show the widest host ranges and many records. The ability of the pathogens to remain latent on asymptomatic plants, and uncontrolled trade of plant materials among countries, facilitate the dissemination and potential introduction of new Botryosphaeriaceae species. Preventive detection and adequate control strategies are always needed to limit the potential damage caused by Botryosphaeriaceae. This review had particular emphasis on host-pathogen associations, disease symptoms, geographic distribution, metabolite production, and accurate pathogen identification.
... The new records will also benefit future studies which cover critical fields including fungal diagnostics and identification, economics and environmental management (Chethana et al. 2021). Several contemporary webpages provide data on fungal taxa from different habitats and regions, including descriptions, illustrations, phylogenetic trees, notes and the current number of accepted species (Pem et al. 2019a;Bundhun et al. 2020;Calabon et al. 2020b;Wijesinghe et al. 2021). ...
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This is a continuation of the papers “Towards a classification of Sordariomycetes” (2015) and “Families of Sordariomycetes” (2016) in which we compile a treatment of the class Sordariomycetes. The present treatment is needed as our knowledge has rapidly increased, from 32 orders, 105 families and 1331 genera in 2016, to 45 orders, 167 families and 1499 genera (with 308 genera incertae sedis) at the time of publication. In this treatment we provide notes on each order, families and short notes on each genus. We provide up-to-date DNA based phylogenies for 45 orders and 163 families. Three new genera and 16 new species are introduced with illustrations and descriptions, while 23 new records and three new species combinations are provided. We also list 308 taxa in Sordariomycetes genera incertae sedis. For each family we provide general descriptions and illustrate the type genus or another genus, the latter where the placement has generally been confirmed with molecular data. Both the sexual and asexual morphs representative of a family are illustrated where available. Notes on ecological and economic considerations are also given.
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In order to establish the phylogenetic relationships and to resolve the natural classification of species in Dothideomycetes, it is necessary to use multi-gene phylogeny as well as morphology. Phaeodothis mori is a new species collected from dead leaves of Morus australis from Chiayi, Taiwan. Maximum parsimony, maximum likelihood and Bayesian analyses were performed based on multi-locus phylogenies of ITS, LSU, SSU and tef1-α to clarify the phylogenetic affinities of the species. Phaeodothis mori is distinguished from the other Phaeodothis species based on distinct size differences in ascomata, asci, ascospores and base pair differences in DNA sequence data. Remarkably, this is the first Phaeodothis species recorded from Morus australis. The new species was compared with the type species of Phaeodothis and a comprehensive description and micrographs were provided.
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This article is the tenth series of the Fungal Diversity Notes, where 114 taxa distributed in three phyla, ten classes, 30 orders and 53 families are described and illustrated. Taxa described in the present study include one new family (viz. Pseudoberkleasmiaceae in Dothideomycetes), five new genera (Caatingomyces, Cryptoschizotrema, Neoacladium, Paramassaria and Trochilispora) and 71 new species, (viz. Acrogenospora thailandica, Amniculicola aquatica, A. guttulata, Angustimassarina sylvatica, Blackwellomyces lateris, Boubovia gelatinosa, Buellia viridula, Caatingomyces brasiliensis, Calophoma humuli, Camarosporidiella mori, Canalisporium dehongense, Cantharellus brunneopallidus, C. griseotinctus, Castanediella meliponae, Coprinopsis psammophila, Cordyceps succavus, Cortinarius minusculus, C. subscotoides, Diaporthe italiana, D. rumicicola, Diatrypella delonicis, Dictyocheirospora aquadulcis, D. taiwanense, Digitodesmium chiangmaiense, Distoseptispora dehongensis, D. palmarum, Dothiorella styphnolobii, Ellisembia aurea, Falciformispora aquatic, Fomitiporia carpinea, F. lagerstroemiae, Grammothele aurantiaca, G. micropora, Hermatomyces bauhiniae, Jahnula queenslandica, Kamalomyces mangrovei, Lecidella yunnanensis, Micarea squamulosa, Muriphaeosphaeria angustifoliae, Neoacladium indicum, Neodidymelliopsis sambuci, Neosetophoma miscanthi, N. salicis, Nodulosphaeria aquilegiae, N. thalictri, Paramassaria samaneae, Penicillium circulare, P. geumsanense, P. mali-pumilae, P. psychrotrophicum, P. wandoense, Phaeoisaria siamensis, Phaeopoacea asparagicola, Phaeosphaeria penniseti, Plectocarpon galapagoense, Porina sorediata, Pseudoberkleasmium chiangmaiense, Pyrenochaetopsis sinensis, Rhizophydium koreanum, Russula prasina, Sporoschisma chiangraiense, Stigmatomyces chamaemyiae, S. cocksii, S. papei, S. tschirnhausii, S. vikhrevii, Thysanorea uniseptata, Torula breviconidiophora, T. polyseptata, Trochilispora schefflerae and Vaginatispora palmae). Further, twelve new combinations (viz. Cryptoschizotrema cryptotrema, Prolixandromyces australi, P. elongatus, P. falcatus, P. longispinae, P. microveliae, P. neoalardi, P. polhemorum, P. protuberans, P. pseudoveliae, P. tenuistipitis and P. umbonatus), an epitype is chosen for Cantharellus goossensiae, a reference specimen for Acrogenospora sphaerocephala and new synonym Prolixandromyces are designated. Twenty-four new records on new hosts and new geographical distributions are also reported (i.e. Acrostalagmus annulatus, Cantharellus goossensiae, Coprinopsis villosa, Dothiorella plurivora, Dothiorella rhamni, Dothiorella symphoricarposicola, Dictyocheirospora rotunda, Fasciatispora arengae, Grammothele brasiliensis, Lasiodiplodia iraniensis, Lembosia xyliae, Morenoina palmicola, Murispora cicognanii, Neodidymelliopsis farokhinejadii, Neolinocarpon rachidis, Nothophoma quercina, Peroneutypa scoparia, Pestalotiopsis aggestorum, Pilidium concavum, Plagiostoma salicellum, Protofenestella ulmi, Sarocladium kiliense, Tetraploa nagasakiensis and Vaginatispora armatispora).