Sequence-Based Species Description and the Role of The

Total Page:16

File Type:pdf, Size:1020Kb

Sequence-Based Species Description and the Role of The More than a handful of dirt: sequence-based species description and the role of the ICN (a response to Seifert) A recent Editorial in IMA Fungus (Seifert 2017) is critical of sequence-based species description (Hawksworth et al. 2016). The Editorial raises more questions than it answers, concerning the nature of discovery, the minimum evidence that should be required to describe species, and the role of the International Code of Nomenclature for algae, fungi, and plants (ICN; McNeill et al. 2012) as an enforcer of taxonomic quality. The Editorial trivializes the work of molecular ecologists and paints a bleak picture of the future of taxonomy if sequence-based species description is adopted. Here, I address some of the questions raised in the Editorial and offer a more optimistic vision for the integration of molecular ecology and taxonomy. Responses to quoted elements (in italics) are below: CORRESPONDENCE 1. As stated by Hibbett et al. (2011), “... for information about unsequenced Yes, the knowledge that someone else molecular ecology is clearly the major arena taxa, including ecology, and geographic has already detected the same DNA of contemporary species discovery...” rather distributions. This newly formed represented by the specimen in hand than conventional taxonomy. My question team might request specimens from does change the picture. First, it means is whether this process actually discovers new herbaria or culture collections to obtain that the species was already discovered. species, or simply indicates that there are new sequences to check whether the newly The taxonomist who has the specimen species to be found? discovered sequences correspond to in hand should be delighted, not species that have already been described. threatened, by this knowledge, because To “discover” something is to become At some point, they might decide that the sequence may provide insights aware that it exists. It is possible to some of the new sequences warrant that can augment information based discover new species through analyses description as new species, but under on the specimen. Most importantly, of sequences as well as specimens. the current rules of nomenclature they the sequence provides information It is a different question to ask if would be unable to validly name their concerning phylogenetic relationships sequences (or specimens) provide discoveries, because they do not have of the species. The phylogeny may make sufficient information to warrant formal a physical type specimen. However, if it possible to predict characteristics that description. the ecologist had saved a portion of are not observable in the specimen, such their handful of dirt then that could as physiological attributes. Information 2. In modern ecology, when you have a serve as type material, as demonstrated about ecology and biogeography can substrate in your hand that contains DNA by the valid publication of Piromyces be derived from metadata about the sequences of a thousand species, half of them cryptodigmaticus (Kirk 2012; but see sequence, including sampling locality unknown, have you discovered 500 new species Tripp & Lendemer 2012). and source material. For example, if or have you picked up a handful of dirt? the specimen is a mushroom growing 3. Does the act of naming a sequence provide on soil and the sequence comes from A molecular ecologist does not simply new information that is not already inherent a root tip then it may be possible to pick up a handful of dirt. They travel in the sequence itself? I would say not. make an inference about the ecology to a sampling locality, collect dirt, of the species. With an environmental record metadata, extract DNA, perform I would say yes. The act of naming sequence in hand, the picture has details shotgun metagenomics or amplicon communicates the information that that might otherwise be invisible. sequencing, feed the sequences through someone thinks they have discovered a bioinformatics pipeline that compares a new species. A DNA sequence is 5. Is there any conceptual similarity between them to millions of other sequences, just a DNA sequence, whereas a name a species based on one specimen and a species make community comparisons using embodies a taxonomic hypothesis based on a few DNA sequences? tools such as UniFrac (Loupozone (including lineage information). One & Knight 2005), and deposit their might just as well ask if the act of This is a red herring. The conceptual new sequences in publicly-accessible naming provides new information that similarity, to the extent there is one, is of databases. This is usually where the is not inherent in a morphological the most general nature, concerning the process ends, without a determination description. nature of evidence that justifies formal that any new species have been naming. This question conflates two discovered. 4. Whether it is one specimen or a hundred, different issues: (1) whether a species How might the research proceed with a specimen in hand it seems clear should be described based on a single if there was a robust feedback loop that you have made a discovery. Does the observation, and (2) whether sequences between fungal taxonomy and knowledge that someone else has detected can serve as the type material. These are molecular ecology? In that alternate the same DNA in a different handful of not equivalent questions. The answer to universe, the ecologist would employ dirt really change the picture? There are no one does not automatically inform the a bioinformatics tool to place the new characters other than nucleotides, there is no answer to the other. sequences in a phylogenetic tree to seek differential ecology or behaviour attributable their closest relatives. The ecologist to the specific unknowns, unless they can be 6. Does a double standard exist, where our might then reach out to a taxonomist inferred in some way by information inherent historical practise [sic] allows (but is now who could consult relevant monographs in the genetic sequences. actively discouraging) what some perceive as (36) IMA FUNGUS low quality species descriptions with an old description based on single collections, discovered – within the groups on CORRESPONDENCE technology, while preventing what some would although that would be consistent which they specialize (they should consider a higher quality of species description with a role as a “quality assurance already be doing this). They would then using a new technology? mechanism”. name only the species for which they In my view, the function of the think there is adequate evidence. For Yes, there is a double standard. A species ICN is to dictate the terms for valid an example, see the thoughtful (not known only from a single collection publication of names, not to assure at all banal or trivial) description of can be validly named, even if the type taxonomic accuracy. “Quality” in fungal Hawksworthiomyces sequentia by De specimen has no observable characters taxonomy is “enforced” by editors Beer et al. (2016). that differentiate it from any other and reviewers, and by the scientific species, has been reduced to dust, or community, particularly authors of 10. When should we describe species? even lost, but a species known by any monographs and other taxonomic number of independent environmental compilations. If taxonomists disapprove The answer to the question posed in the sequences, with metadata, cannot be of sequence-based species, then they title of the Editorial is that taxonomists validly named. The absurdity of this should exclude them from their should describe species whenever they double standard will become all the monographs and checklists. However, think that it is warranted based on the more evident as techniques such as the rules of nomenclature should not evidence at hand. Different taxonomists single-cell genomics become more prohibit other workers from formalizing will have different standards for widely used in ecological studies. hypotheses based on sequences as valid evidence that justifies species names with the protection of priority. description. One author might insist 7. Are the limitations of what we can By the same reasoning, the ICN on several collections and multi-gene determine about a species from a DNA should not prohibit species description phylogenies with Bayesian coalescent sequence more severe than what we can based on a single specimen (or require analyses. Another may think that a determine about a species when we have sequence data). single specimen without molecular only one specimen? If not, why are so many data is sufficient. A third may be happy journals reluctant to allow single species 9. What does it take to raise species description with multiple environmental sequences, descriptions based on morphology, but lining above banality, above trivia that could be backed up by metadata and phylogenetic up to publish controversial papers on DNA extracted by any child or by a machine? analyses, as per the proposed defines[sic] taxa that test the limits of the Do we want machine taxonomy in fungal Recommendations for sequence-based ICN? biology? From one perspective this seems typification by Hawksworth et al. like a paranoid question and, from another, (2016). Currently, the ICN would See (5) regarding single specimens vs. prescient. If DNA sequences comprise both permit the first two authors to formally sequences in species description. The the description and the type, it is a short step name their hypotheses, which would suggestion that “so many” journals to a pipeline that automatically describes then receive the protection of priority, are “lining up to publish” papers on and names the OTUs as species. The question but the third author would not have sequence-based species description is of machine-automated species description that option. This borders on scientific an exaggeration. Even the most casual is staring us in the face. Surely we should be chauvinism, and is inconsistent with the perusal of current literature shows that discussing it? principles of the ICN, which has never sequence-based species descriptions dictated the nature of evidence required are extremely rare (perhaps because Yes, this does sound paranoid.
Recommended publications
  • Molecular Systematics of the Marine Dothideomycetes
    available online at www.studiesinmycology.org StudieS in Mycology 64: 155–173. 2009. doi:10.3114/sim.2009.64.09 Molecular systematics of the marine Dothideomycetes S. Suetrong1, 2, C.L. Schoch3, J.W. Spatafora4, J. Kohlmeyer5, B. Volkmann-Kohlmeyer5, J. Sakayaroj2, S. Phongpaichit1, K. Tanaka6, K. Hirayama6 and E.B.G. Jones2* 1Department of Microbiology, Faculty of Science, Prince of Songkla University, Hat Yai, Songkhla, 90112, Thailand; 2Bioresources Technology Unit, National Center for Genetic Engineering and Biotechnology (BIOTEC), 113 Thailand Science Park, Paholyothin Road, Khlong 1, Khlong Luang, Pathum Thani, 12120, Thailand; 3National Center for Biothechnology Information, National Library of Medicine, National Institutes of Health, 45 Center Drive, MSC 6510, Bethesda, Maryland 20892-6510, U.S.A.; 4Department of Botany and Plant Pathology, Oregon State University, Corvallis, Oregon, 97331, U.S.A.; 5Institute of Marine Sciences, University of North Carolina at Chapel Hill, Morehead City, North Carolina 28557, U.S.A.; 6Faculty of Agriculture & Life Sciences, Hirosaki University, Bunkyo-cho 3, Hirosaki, Aomori 036-8561, Japan *Correspondence: E.B. Gareth Jones, [email protected] Abstract: Phylogenetic analyses of four nuclear genes, namely the large and small subunits of the nuclear ribosomal RNA, transcription elongation factor 1-alpha and the second largest RNA polymerase II subunit, established that the ecological group of marine bitunicate ascomycetes has representatives in the orders Capnodiales, Hysteriales, Jahnulales, Mytilinidiales, Patellariales and Pleosporales. Most of the fungi sequenced were intertidal mangrove taxa and belong to members of 12 families in the Pleosporales: Aigialaceae, Didymellaceae, Leptosphaeriaceae, Lenthitheciaceae, Lophiostomataceae, Massarinaceae, Montagnulaceae, Morosphaeriaceae, Phaeosphaeriaceae, Pleosporaceae, Testudinaceae and Trematosphaeriaceae. Two new families are described: Aigialaceae and Morosphaeriaceae, and three new genera proposed: Halomassarina, Morosphaeria and Rimora.
    [Show full text]
  • Morphological and Molecular Characterisation of Periconia Pseudobyssoides Sp
    Mycol Progress DOI 10.1007/s11557-013-0914-6 ORIGINAL ARTICLE Morphological and molecular characterisation of Periconia pseudobyssoides sp. nov. and closely related P. byssoides Svetlana Markovskaja & Audrius Kačergius Received: 23 April 2013 /Revised: 26 June 2013 /Accepted: 9 July 2013 # German Mycological Society and Springer-Verlag Berlin Heidelberg 2013 Abstract Anamorphic ascomycetes of the genus Periconia, and in other European countries, 34 species of anamorphic occurring on invasive Heracleum sosnowskyi and on other fungi was established, including Periconia spp. which frequent- native Apiaceae plants were examined during this study. On ly occurred. Part of Periconia specimens were identified as P. the basis of morphological, cultural characteristics and ITS byssoides Pers., which is widely distributed on Apiaceae and sequences a new species of Periconia closely related to other herbaceous plants, but several specimens differed from P. Periconia byssoides, is described and illustrated. The new byssoides and other known Periconia species by morphological species Periconia pseudobyssoides, collected on dead stalks and cultural characters. These specimens represented a separate of Heracleum sosnowskyi, is characterized by producing taxonomic entity which is proposed here as a new species. brownish verruculose mycelium on malt-extract agar, and Most Periconia species are widely distributed terrestrial differs from P. byssoides and other known Periconia species saprobes and endophytes colonizing herbaceous and woody by producing reddish-brown, macronematous conidiophores plants in various geographical regions and habitats (Ellis with numerous percurrent proliferations, often verruculose at 1971, 1976;Matsushima1971, 1975, 1980, 1989, 1996;Rao the apex immediately below the conidial head, verrucose and Rao 1964;Subramanian1955; Subrahmanyam 1980; ovoid conidiogenous cells arising directly from the swollen Lunghini 1978; Saikia and Sarbhoy 1982; Muntañola- apical cell cut off by a septum from the stipe apex, and Cvetković et al.
    [Show full text]
  • 臺灣紅樹林海洋真菌誌 林 海 Marine Mangrove Fungi 洋 真 of Taiwan 菌 誌 Marine Mangrove Fungimarine of Taiwan
    臺 灣 紅 樹 臺灣紅樹林海洋真菌誌 林 海 Marine Mangrove Fungi 洋 真 of Taiwan 菌 誌 Marine Mangrove Fungi of Taiwan of Marine Fungi Mangrove Ka-Lai PANG, Ka-Lai PANG, Ka-Lai PANG Jen-Sheng JHENG E.B. Gareth JONES Jen-Sheng JHENG, E.B. Gareth JONES JHENG, Jen-Sheng 國 立 臺 灣 海 洋 大 G P N : 1010000169 學 售 價 : 900 元 臺灣紅樹林海洋真菌誌 Marine Mangrove Fungi of Taiwan Ka-Lai PANG Institute of Marine Biology, National Taiwan Ocean University, 2 Pei-Ning Road, Chilung 20224, Taiwan (R.O.C.) Jen-Sheng JHENG Institute of Marine Biology, National Taiwan Ocean University, 2 Pei-Ning Road, Chilung 20224, Taiwan (R.O.C.) E. B. Gareth JONES Bioresources Technology Unit, National Center for Genetic Engineering and Biotechnology (BIOTEC), 113 Thailand Science Park, Phaholyothin Road, Khlong 1, Khlong Luang, Pathumthani 12120, Thailand 國立臺灣海洋大學 National Taiwan Ocean University Chilung January 2011 [Funded by National Science Council, Taiwan (R.O.C.)-NSC 98-2321-B-019-004] Acknowledgements The completion of this book undoubtedly required help from various individuals/parties, without whom, it would not be possible. First of all, we would like to thank the generous financial support from the National Science Council, Taiwan (R.O.C.) and the center of Excellence for Marine Bioenvironment and Biotechnology, National Taiwan Ocean University. Prof. Shean- Shong Tzean (National Taiwan University) and Dr. Sung-Yuan Hsieh (Food Industry Research and Development Institute) are thanked for the advice given at the beginning of this project. Ka-Lai Pang would particularly like to thank Prof.
    [Show full text]
  • A Polyphasic Approach to Characterise Phoma and Related Pleosporalean Genera
    available online at www.studiesinmycology.org StudieS in Mycology 65: 1–60. 2010. doi:10.3114/sim.2010.65.01 Highlights of the Didymellaceae: A polyphasic approach to characterise Phoma and related pleosporalean genera M.M. Aveskamp1, 3*#, J. de Gruyter1, 2, J.H.C. Woudenberg1, G.J.M. Verkley1 and P.W. Crous1, 3 1CBS-KNAW Fungal Biodiversity Centre, Uppsalalaan 8, 3584 CT Utrecht, The Netherlands; 2Dutch Plant Protection Service (PD), Geertjesweg 15, 6706 EA Wageningen, The Netherlands; 3Wageningen University and Research Centre (WUR), Laboratory of Phytopathology, Droevendaalsesteeg 1, 6708 PB Wageningen, The Netherlands *Correspondence: Maikel M. Aveskamp, [email protected] #Current address: Mycolim BV, Veld Oostenrijk 13, 5961 NV Horst, The Netherlands Abstract: Fungal taxonomists routinely encounter problems when dealing with asexual fungal species due to poly- and paraphyletic generic phylogenies, and unclear species boundaries. These problems are aptly illustrated in the genus Phoma. This phytopathologically significant fungal genus is currently subdivided into nine sections which are mainly based on a single or just a few morphological characters. However, this subdivision is ambiguous as several of the section-specific characters can occur within a single species. In addition, many teleomorph genera have been linked to Phoma, three of which are recognised here. In this study it is attempted to delineate generic boundaries, and to come to a generic circumscription which is more correct from an evolutionary point of view by means of multilocus sequence typing. Therefore, multiple analyses were conducted utilising sequences obtained from 28S nrDNA (Large Subunit - LSU), 18S nrDNA (Small Subunit - SSU), the Internal Transcribed Spacer regions 1 & 2 and 5.8S nrDNA (ITS), and part of the β-tubulin (TUB) gene region.
    [Show full text]
  • Pseudodidymosphaeria Gen. Nov. in Massarinaceae
    Phytotaxa 231 (3): 271–282 ISSN 1179-3155 (print edition) www.mapress.com/phytotaxa/ PHYTOTAXA Copyright © 2015 Magnolia Press Article ISSN 1179-3163 (online edition) http://dx.doi.org/10.11646/phytotaxa.231.3.5 Pseudodidymosphaeria gen. nov. in Massarinaceae KASUN M. THAMBUGALA1, 2, 3, YU CHUNFANG4, ERIO CAMPORESI5, ALI H. BAHKALI6, ZUO-YI LIU1, * & KEVIN D. HYDE2, 3 1Guizhou Key Laboratory of Agricultural Biotechnology, Guizhou Academy of Agricultural Sciences, Xiaohe District, Guiyang City, Guizhou Province 550006, People’s Republic of China 2Institute of Excellence in Fungal Research, Mae Fah Luang University, Chiang Rai 57100, Thailand 3School of Science, Mae Fah Luang University, Chiang Rai. 57100, Thailand 4Institute of Basic Medical Sciences, Hubei University of Medicine, shiyan, Hubei Province, 442000, People’s Republic of China 5A.M.B. Gruppo Micologico Forlivese “Antonio Cicognani”, Via Roma 18, Forlì, Italy; A.M.B. Circolo Micologico “Giovanni Carini”, C.P. 314, Brescia, Italy 6Department of Botany and Microbiology, King Saudi University, Riyadh, Saudi Arabia *Corresponding author: email: [email protected] Abstract Didymosphaeria spartii was collected from dead branches of Spartium junceum in Italy. Multi-gene phylogenetic analyses of ITS, 18S and 28S nrDNA sequence data were carried out using maximum likelihood and Bayesian analysis. The resulting phylogenetic trees showed this to be a new genus in a well-supported clade in Massarinaceae. A new genus Pseudodidymo- sphaeria is therefore introduced to accommodate this species based on molecular phylogeny and morphology. A illustrated account is provided for the new genus with its asexual morph and the new taxon is compared with Massarina and Didymo- sphaeria.
    [Show full text]
  • A World Revision of Massarina (Ascomycota)
    Nova Hedwigia 66 1—2 89—162 Stuttgart, Februar 1998 A world revision of Massarina (Ascomycota) by Andre Aptroot Centraalbureau voor Schimmelcultures P.O. Box 273, NL-3740 AG Baarn, The Netherlands With 46 figures Aptroot, A. (1998): A world revision of Massarina (Ascomycota) - Nova Hedwigia 89-162. Abstract: A world revision of the pyrenocarpous ascomycete genus Massarina (Lophiostomataceae, Pleosporales) accepting 43 species is presented. The genera Epiphegia and Oraniella are reinstated. Sever• al species formerly classified in Massarina were found to belong to Exarmidium, of which Xylopezia is found to be a synonym. Several other species are excluded from the genus; most of them were found to be synonymous with other taxa, including many lichens. The following new combinations are pro• posed: Anisomeridium grumatum (Cooke) Aptroot, Epiphegia microcarpa (Fuckel) Aptroot, Exarmidi• um biseptatum (Sherwood) Aptroot, E. excellens (Rehm ex Saccardo) Aptroot, E. hemisphaericum (Fries:Fries) Aptroot, E. inclusum (Persoon) Aptroot, Massarina igniaria (C. Booth) Aptroot, Pseudo- pyrenula staphyleae (Petrak) Aptroot, Splanchnonema quinqueseptatum (M. Barr) Aptroot, Wettsteini- na corni (Fuckel) Aptroot, and W. xerophylli (Ellis) Aptroot. Key words: Ascomycetes, Massarina, Lophiostomataceae, Pleosporales, Epiphegia, Oraniella, Xylope• zia, Anisomeridium, Exarmidium, Pseudopyrenula, Splanchnonema, Wettsteinina, lichens, revision. Introduction and History The genus Massarina Saccardo (1883) was erected for species of pyrenocarpous as• comycetes segregated from Massaria De Notaris by having hyaline ascospores. Among the original species, the most common species of the genus as presently cir• cumscribed, M. eburnea (Tulasne & C. Tulasne) Saccardo, was selected as lectotype of the genus by Clements and Shear (1931). The genus was ranked in a separate family, the Massarinaceae Munk, by Munk (1956), but it is now regarded as belonging to the Lophiostomataceae Saccardo in the Pleosporales, according to Barr (1992).
    [Show full text]
  • Multi-Locus Phylogeny of Pleosporales: a Taxonomic, Ecological and Evolutionary Re-Evaluation
    available online at www.studiesinmycology.org StudieS in Mycology 64: 85–102. 2009. doi:10.3114/sim.2009.64.04 Multi-locus phylogeny of Pleosporales: a taxonomic, ecological and evolutionary re-evaluation Y. Zhang1, C.L. Schoch2, J. Fournier3, P.W. Crous4, J. de Gruyter4, 5, J.H.C. Woudenberg4, K. Hirayama6, K. Tanaka6, S.B. Pointing1, J.W. Spatafora7 and K.D. Hyde8, 9* 1Division of Microbiology, School of Biological Sciences, The University of Hong Kong, Pokfulam Road, Hong Kong SAR, P.R. China; 2National Center for Biotechnology Information, National Library of Medicine, National Institutes of Health, 45 Center Drive, MSC 6510, Bethesda, Maryland 20892-6510, U.S.A.; 3Las Muros, Rimont, Ariège, F 09420, France; 4CBS-KNAW Fungal Biodiversity Centre, P.O. Box 85167, 3508 AD, Utrecht, The Netherlands; 5Plant Protection Service, P.O. Box 9102, 6700 HC Wageningen, The Netherlands; 6Faculty of Agriculture & Life Sciences, Hirosaki University, Bunkyo-cho 3, Hirosaki, Aomori 036-8561, Japan; 7Department of Botany and Plant Pathology, Oregon State University, Corvallis, Oregon 93133, U.S.A.; 8School of Science, Mae Fah Luang University, Tasud, Muang, Chiang Rai 57100, Thailand; 9International Fungal Research & Development Centre, The Research Institute of Resource Insects, Chinese Academy of Forestry, Kunming, Yunnan, P.R. China 650034 *Correspondence: Kevin D. Hyde, [email protected] Abstract: Five loci, nucSSU, nucLSU rDNA, TEF1, RPB1 and RPB2, are used for analysing 129 pleosporalean taxa representing 59 genera and 15 families in the current classification ofPleosporales . The suborder Pleosporineae is emended to include four families, viz. Didymellaceae, Leptosphaeriaceae, Phaeosphaeriaceae and Pleosporaceae. In addition, two new families are introduced, i.e.
    [Show full text]
  • Two New Ascomycetes with Long Gelatinous Appendages Collected from Monocots in the Tropics
    STUDIES IN MYCOLOGY 50: 307–311. 2004. Two new ascomycetes with long gelatinous appendages collected from monocots in the tropics André Aptroot* Centraalbureau voor Schimmelcultures, P.O. Box 85167, NL-3508 AD Utrecht, The Netherlands *Correspondence: A. Aptroot, [email protected] Abstract: Two new ascomycetes with long gelatinous appendages on brown 1- or 2-septate ascospores are described from monocots in the tropics. The new genus Funiliomyces with the single species F. biseptatus from a Bromeliaceae leaf from Brazil belongs to the Amphisphaeriales, according to morphology and phylogenetic reconstruction using LSU sequence data. It is characterised by the torpedo-shaped ascospores with two nearly central septa and one polar and one median appendage. The new species Munkovalsaria appendiculata from dead culms of Zea mays in Hong Kong is characterised by its long polar appendages. The genus Munkovalsaria, originally assigned to the Dothideales, clusters with high bootstrap support in the Pleosporales, and should consequently be assigned to that order. Both new species have a saprobic life style and are truly terrestrial. This is remarkable, because most ascomycetes with ascospores possessing long appendages occur in freshwater or in the marine environment. Taxonomic novelties: Funiliomyces biseptatus Aptroot gen. et sp. nov., Munkovalsaria appendiculata Aptroot sp. nov. Key words: Amphisphaeriales, ascomycetes, Brazil, Bromeliaceae, Funiliomyces, Hong Kong, ITS, LSU, monocots, Munko- valsaria, taxonomy, Zea INTRODUCTION the species was repositioned in other genera by Ap- troot (1995b), including the new genus Munkovalsaria Ascomycetes with extracellular, often gelatinous, with two accepted species. Few species of Didymo- appendages on the ascospores are mostly known from sphaeria have been described since the monograph by aquatic habitats.
    [Show full text]
  • Bibliografía Botánica Del Caribe I
    Consolidated bibliography Introduction To facilitate the search through the bibliographies prepared by T. Zanoni (Bibliographía botánica del Caribe, Bibliografía de la flora y de la vegetatíon de la isla Española, and the Bibliography of Carribean Botany series currently published in the Flora of Greater Antilles Newsletter), the html versions of these files have been put together in a single pdf file. The reader should note the coverage of each bibliography: Hispaniola is exhaustively covered by all three bibliographies (from the origin up to now) while other areas of the Carribean are specifically treated only since 1984. Please note that this pdf document is made from multiple documents, this means that search function is called by SHIFT+CTRL+F (rather than by CTRL+F). Please let me know of any problem. M. Dubé The Jardín Botánico Nacional "Dr. Rafael M. Moscoso," Santo Domingo, Dominican Republic, publishers of the journal Moscosoa, kindly gave permission for the inclusion of these bibliographies on this web site. Please note the present address of T. Zanoni : New York Botanical Garden 200th Street at Southern Blvd. Bronx, NY 10458-5126, USA email: [email protected] Moscosoa 4, 1986, pp. 49-53 BIBLIOGRAFÍA BOTÁNICA DEL CARIBE. 1. Thomas A. Zanoni Zanoni. Thomas A. (Jardín Botánico Nacional, Apartado 21-9, Santo Domingo, República Dominicana). Bibliografía botánica del Caribe. 1. Moscosoa 4: 49-53. 1986. Una bibliografía anotada sobre la literatura botánica publicada en los años de 1984 y 1985. Se incluyen los temas de botánica general y la ecología de las plantas de las islas del Caribe. An annotated bibliography of the botanical literature published in 1984 and 1985, covering all aspects of botany and plant ecology of the plants of the Caribbean Islands.
    [Show full text]
  • Checklist of Fungi on Teak
    Mycosphere 7 (5):656–678 (2016) www.mycosphere.org ISSN 2077 7019 Article Doi 10.5943/mycosphere/7/5/11 Copyright © Guizhou Academy of Agricultural Sciences Checklist of fungi on teak Doilom M1, Taylor JE2, Bhat DJ3, Chukeatirote E1, Hyde KD1, To-anun C4 and Jones EBG4,5 1 Center of Excellence in Fungal Research, and School of Science, Mae Fah Luang University, Chiang Rai 57100, Thailand 2 Royal Botanic Garden Edinburgh, 20A Inverleith Row, Edinburgh, EH3 5LR, United Kingdom 3 No. 128/1–J, Azad Housing Society, Curca, Goa Velha, India 4 Department of Entomology and Plant Pathology, Faculty of Agriculture, Chiang Mai University, Chiangmai 50200, Thailand 5 Department of Botany and Microbiology, College of Science, King Saud University, P.O. Box: 2455, Riyadh 1145, Saudi Arabia Doilom M, Taylor JE, Bhat DJ, Chukeatirote E, Hyde KD, To-anun C, Jones EBG 2016 – Checklist of fungi on teak. Mycosphere 7(5), 656–678, Doi 10.5943/mycosphere/7/5/11 Abstract This publication provides an updated checklist of fungi on teak. This is a compilation of information on substrate and locality from where fungi have been recorded on teak, or original descriptions available. In total, 152 species with 34 hitherto unidentified species are listed here on teak, from 39 countries. The fungi recorded from teak are distributed in 32 orders, 69 families, 134 genera, which can be divided into two taxonomic groups: (i) Ascomycota: 23 orders, 54 families, 114 genera, 132 species identified and 29 unidentified species, and (ii) Basidiomycota: 9 orders, 15 families, 20 genera, 20 species identified and 5 unidentified species.
    [Show full text]
  • Fungal Biodiversity Profiles 11-20
    Cryptogamie, Mycologie, 2015, 36 (3): 355-380 © 2015 Adac. Tous droits réservés Fungal Biodiversity Profiles 11-20 Sinang HONGSANAN a,b,c, Kevin D. HYDE a,b,c,d, Ali H. BAHKALI d, Erio CAMPORESI j, Putaruk CHOMNUNTI c, Hasini EKANAYAKA a,b,c, André A.M. GOMES f, Valérie HOFSTETTER h, E.B.Gareth JONES e, Danilo B. PINHO g, Olinto L. PEREIRA g, Qing TIAN a,b,c, Dhanushka N. WANASINGHE a,b,c, Jian-Chu XU a,b & Bart BUYCK i* aWorld Agroforestry Centre, East and Central Asia, Kunming 650201, Yunnan, China bKey Laboratory of Economic Plants and Biotechnology, Kunming Institute of Botany, Chinese Academy of Sciences, Lanhei Road No 132, Panlong District, Kunming, Yunnan Province, 650201, PR China cCenter of Excellence in Fungal Research, Mae Fah Luang University, Chiang Rai, 57100, Thailand, email address: [email protected] dBotany and Microbiology Department, College of Science, King Saud University, Riyadh, KSA 11442, Saudi Arabia eDepartment of Botany and Microbiology, College of Science, King Saud University, P.O. Box 2455 Riyadh 11451, Kingdom of Saudi Arabia fDepartamento de Microbiologia, Universidade Federal de Viçosa, Viçosa, Minas Gerais, Brazil gDepartamento de Fitopatologia, Universidade Federal de Viçosa, Viçosa, Minas Gerais, Brazil; e-mail: [email protected] hDepartment of plant protection, Agroscope Changins-Wadenswil Research Station, ACW, Rte de Duiller, 1260, Nyon, Switzerland iMuseum National d’Histoire Naturelle, Dept. Systematique et Evolution CP 39, ISYEB, UMR 7205 CNRS MNHN UPMC EPHE, 12 Rue Buffon, F-75005 Paris, France; email: [email protected] jA.M.B. Gruppo Micologico Forlivese “Antonio Cicognani”, Via Roma 18, Forlì, Italy Abstract – The authors describe ten new taxa for science using mostly both morphological and molecular data.
    [Show full text]
  • Evaluation of Groundnut (Arachis Hypogaea L.) Germplasm for Resistance to Leaf Diseases and Related Cytoplasmic Factors, Testa Colour and Cup Leaf
    EVALUATION OF GROUNDNUT (ARACHIS HYPOGAEA L.) GERMPLASM FOR RESISTANCE TO LEAF DISEASES AND RELATED CYTOPLASMIC FACTORS, TESTA COLOUR AND CUP LEAF A. E. Pretorius 2006 EVALUATION OF GROUNDNUT (ARACHIS HYPOGAEA L.) GERMPLASM FOR RESISTANCE TO LEAF DISEASES AND RELATED CYTOPLASMIC FACTORS, TESTA COLOUR AND CUP LEAF by Alana Elmarie Pretorius Submitted in the fulfilment of the requirements of the degree Magister Scientiae Agriculturae In the Department of Plant Sciences (Plant Breeding) Faculty of Natural and Agricultural Sciences University of the Free State Supervisor: Prof M.T. Labuschagne Co-supervisor: Dr M.M. Liebenberg May 2006 Bloemfontein South Africa ii CONTENTS CONTENTS ii ACKNOWLEDGEMENTS viii ABBREVIATIONS AND ACRONYMS ix CHAPTER 1 1 INTRODUCTION 1 CHAPTER 2 A REVIEW OF FOLIAR DISEASES ON GROUNDNUT AND 5 RELATED CYTOPLASMIC FACTORS, TESTA COLOUR AND CUP LEAF INTRODUCTION 5 2.1 FOLIAR DISEASES 7 A. EARLY LEAF SPOT 7 Morphology 7 Disease cycle and dissemination 7 Survival 8 Symptoms 9 Economic importance 9 Disease management 10 Fungicides 10 Breeding for resistance 12 Farming practices 14 Biological control 14 Association between ELS and web blotch (WB) 15 Association between ELS and late leaf spot (LLS) 15 B. LATE LEAF SPOT 16 Morphology 16 Disease cycle and dissemination 17 Survival 18 Symptoms 18 Economic importance 19 Disease management 19 Fungicides 19 Breeding for resistance 21 Farming practices 23 Biological control 23 Association between LLS and rust 24 C. WEB BLOTCH 24 Morphology 24 Disease cycle and dissemination 25 Survival 26 Symptoms 26 iii Economic importance 26 Disease management 27 Fungicides 27 Breeding for resistance 28 Farming practices 28 Association between WB and ELS 29 D.
    [Show full text]