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      Singleton-based species names and fungal rarity: Does the number really matter?

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          Abstract

          Fungi are among the least known organisms on earth, with an estimated number of species between 1.5 and 10 million. This number is expected to be refined, especially with increasing knowledge about microfungi in undersampled habitats and increasing amounts of data derived from environmental DNA sequencing. A significant proportion of newly generated sequences fail to match with already named species, and thus represent what has been referred to as fungal “dark taxa”. Due to the challenges associated with observing, identifying, and preserving sporophores, many macro- and microfungal species are only known from a single collection, specimen, isolate, and/or sequence—a singleton. Mycologists are consequently used to working with “rare” sequences and specimens. However, rarity and singleton phenomena lack consideration and valorization in fungal studies. In particular, the practice of publishing new fungal species names based on a single specimen remains a cause of debate. Here, we provide some elements of reflection on this issue in the light of the specificities of the fungal kingdom and global change context. If multiple independent sources of data support the existence of a new taxon, we encourage mycologists to proceed with formal description, irrespective of the number of specimens at hand. Although the description of singleton-based species may not be considered best practice, it does represent responsible science in the light of closing the Linnean biodiversity shortfall.

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          Nuclear ribosomal internal transcribed spacer (ITS) region as a universal DNA barcode marker for Fungi.

          Six DNA regions were evaluated as potential DNA barcodes for Fungi, the second largest kingdom of eukaryotic life, by a multinational, multilaboratory consortium. The region of the mitochondrial cytochrome c oxidase subunit 1 used as the animal barcode was excluded as a potential marker, because it is difficult to amplify in fungi, often includes large introns, and can be insufficiently variable. Three subunits from the nuclear ribosomal RNA cistron were compared together with regions of three representative protein-coding genes (largest subunit of RNA polymerase II, second largest subunit of RNA polymerase II, and minichromosome maintenance protein). Although the protein-coding gene regions often had a higher percent of correct identification compared with ribosomal markers, low PCR amplification and sequencing success eliminated them as candidates for a universal fungal barcode. Among the regions of the ribosomal cistron, the internal transcribed spacer (ITS) region has the highest probability of successful identification for the broadest range of fungi, with the most clearly defined barcode gap between inter- and intraspecific variation. The nuclear ribosomal large subunit, a popular phylogenetic marker in certain groups, had superior species resolution in some taxonomic groups, such as the early diverging lineages and the ascomycete yeasts, but was otherwise slightly inferior to the ITS. The nuclear ribosomal small subunit has poor species-level resolution in fungi. ITS will be formally proposed for adoption as the primary fungal barcode marker to the Consortium for the Barcode of Life, with the possibility that supplementary barcodes may be developed for particular narrowly circumscribed taxonomic groups.
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            Towards a unified paradigm for sequence-based identification of fungi.

            The nuclear ribosomal internal transcribed spacer (ITS) region is the formal fungal barcode and in most cases the marker of choice for the exploration of fungal diversity in environmental samples. Two problems are particularly acute in the pursuit of satisfactory taxonomic assignment of newly generated ITS sequences: (i) the lack of an inclusive, reliable public reference data set and (ii) the lack of means to refer to fungal species, for which no Latin name is available in a standardized stable way. Here, we report on progress in these regards through further development of the UNITE database (http://unite.ut.ee) for molecular identification of fungi. All fungal species represented by at least two ITS sequences in the international nucleotide sequence databases are now given a unique, stable name of the accession number type (e.g. Hymenoscyphus pseudoalbidus|GU586904|SH133781.05FU), and their taxonomic and ecological annotations were corrected as far as possible through a distributed, third-party annotation effort. We introduce the term 'species hypothesis' (SH) for the taxa discovered in clustering on different similarity thresholds (97-99%). An automatically or manually designated sequence is chosen to represent each such SH. These reference sequences are released (http://unite.ut.ee/repository.php) for use by the scientific community in, for example, local sequence similarity searches and in the QIIME pipeline. The system and the data will be updated automatically as the number of public fungal ITS sequences grows. We invite everybody in the position to improve the annotation or metadata associated with their particular fungal lineages of expertise to do so through the new Web-based sequence management system in UNITE. © 2013 John Wiley & Sons Ltd.
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              The magnitude of fungal diversity: the 1.5 million species estimate revisited

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                Author and article information

                Contributors
                cazabonne.jonathan@gmail.com
                danny.haelewaters@gmail.com
                Journal
                IMA Fungus
                IMA Fungus
                IMA Fungus
                BioMed Central (London )
                2210-6340
                2210-6359
                20 March 2024
                20 March 2024
                2024
                : 15
                : 7
                Affiliations
                [1 ]Ecology Research Group of Abitibi RCM, Forest Research Institute, Université du Québec en Abitibi-Témiscamingue, ( https://ror.org/02mqrrm75) Amos, QC J9T 2L8 Canada
                [2 ]Centre for Forest Research, Université du Québec à Montréal, ( https://ror.org/002rjbv21) Montreal, QC H3C 3P8 Canada
                [3 ]Department of Biology, Acadia University, ( https://ror.org/00839we02) Wolfville, NS B4P 2R6 Canada
                [4 ]GRID grid.493090.7, ISNI 0000 0004 4910 6615, Laboratoire Chrono-Environnement, UMR 6249 CNRS, , Université de Bourgogne Franche-Comté, ; 25000 Besançon, France
                [5 ]Forest Research Institute, Université du Québec en Abitibi-Témiscamingue, ( https://ror.org/02mqrrm75) Rouyn-Noranda, QC J9X 5E4 Canada
                [6 ]Research Group Mycology, Department of Biology, Ghent University, ( https://ror.org/00cv9y106) 9000 Ghent, Belgium
                [7 ]GRID grid.14509.39, ISNI 0000 0001 2166 4904, Faculty of Science, , University of South Bohemia, ; 370 05 Ceske Budejovice, Czech Republic
                [8 ]Department of Ecology and Evolutionary Biology, University of Colorado Boulder, ( https://ror.org/02ttsq026) Boulder, CO 80309 USA
                [9 ]GRID grid.447761.7, ISNI 0000 0004 0396 9503, Biology Centre of the Czech Academy of Sciences, , Institute of Entomology, ; 370 05 Ceske Budejovice, Czech Republic
                Author information
                http://orcid.org/0000-0002-6424-0834
                Article
                137
                10.1186/s43008-023-00137-2
                10953280
                38504339
                8db61b28-9ba8-45f6-9542-475f1019ffc9
                © The Author(s) 2024

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 27 August 2023
                : 13 December 2023
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100003130, Fonds Wetenschappelijk Onderzoek;
                Award ID: Senior Postdoctoral Fellowship 1206024N
                Award Recipient :
                Funded by: the European Union’s Horizon 2020 project INTERACT
                Award ID: 871120
                Categories
                MycoLens
                Custom metadata
                © International Mycological Association 2024

                Plant science & Botany
                integrative taxonomy,morphology,rarity,sequencing,singletons,species descriptions

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