Nomenclatural type definitions are one of the most important concepts in biological nomenclature. Being physical objects that can be re-studied by other researchers, types permanently link taxonomy (an artificial agreement to classify biological diversity) with nomenclature (an artificial agreement to name biological diversity). Two proposals to amend the International Code of Nomenclature for algae, fungi, and plants (ICN), allowing DNA sequences alone (of any region and extent) to serve as types of taxon names for voucherless fungi (mainly putative taxa from environmental DNA sequences), have been submitted to be voted on at the 11th International Mycological Congress (Puerto Rico, July 2018). We consider various genetic processes affecting the distribution of alleles among taxa and find that alleles may not consistently and uniquely represent the species within which they are contained. Should the proposals be accepted, the meaning of nomenclatural types would change in a fundamental way from physical objects as sources of data to the data themselves. Such changes are conducive to irreproducible science, the potential typification on artefactual data, and massive creation of names with low information content, ultimately causing nomenclatural instability and unnecessary work for future researchers that would stall future explorations of fungal diversity. We conclude that the acceptance of DNA sequences alone as types of names of taxa, under the terms used in the current proposals, is unnecessary and would not solve the problem of naming putative taxa known only from DNA sequences in a scientifically defensible way. As an alternative, we highlight the use of formulas for naming putative taxa (candidate taxa) that do not require any modification of the ICN.
With the change to one scientific name for pleomorphic fungi, generic names typified by sexual and asexual morphs have been evaluated to recommend which name to use when two names represent the same genus and thus compete for use. In this paper, generic names in Pucciniomycotina and Ustilaginomycotina are evaluated based on their type species to determine which names are synonyms. Twenty-one sets of sexually and asexually typified names in Pucciniomycotina and eight sets in Ustilaginomycotina were determined to be congeneric and compete for use. Recommendations are made as to which generic name to use. In most cases the principle of priority is followed. However, eight generic names in the Pucciniomycotina, and none in Ustilaginomycotina, are recommended for protection: Classicula over Naiadella, Gymnosporangium over Roestelia, Helicobasidium over Thanatophytum and Tuberculina, Melampsorella over Peridermium, Milesina over Milesia, Phragmidium over Aregma, Sporobolomyces over Blastoderma and Rhodomyces, and Uromyces over Uredo. In addition, eight new combinations are made: Blastospora juruensis, B. subneurophyla, Cronartium bethelii, C. kurilense, C. sahoanum, C. yamabense, Milesina polypodii, and Prospodium crusculum combs. nov.
Asterinaceae are small obligately biotrophic pathogens growing superficially on living leaves of higher plants in tropical and subtropical regions worldwide. The species-rich but rarely studied ascomycete group has an uncertain placement within the Dothideomycetes because molecular data are missing completely up to now. Based on nuclear DNA from fresh material of five Asterina spp. and a related anamorphic stage from Panama, we present the first molecular phylogenetic hypothesis of the Asterinaceae within the Dothideomycetes. A combined SSU and LSU rDNA phylogenetic analysis shows that species of Asterina and its anamorphs form a well supported monophyletic clade within the Dothideomycetes with Venturiaceae as sistergroup. Three Asterina spp. included in the molecular study are new records for Panama and Central America with new records of host plant species: A. cestricola on Cestrum rugulosum (Solanaceae), A. weinmanniae on Weinmannia pinnata (Cunoniaceae) and A. zanthoxyli on Zanthoxylum scheryi (Rutaceae). A. cestricola and A. weinmanniae are illustrated here for the first time.
Cercosporella and Ramularia (hyphomycetous anamorphs with relationship to Mycosphaerellaceae, Ascomycota) are difficult to distinguish based on light microscopic characteristics of conidiophores and conidia. Although both genera have been known for more than 120 y, new morphological characteristics were found by "simple" light and scanning electron microscopy now allowing an unambiguous differentiation between both genera. Newly discovered morphological characteristics of interaction structures and ultrastructure of conidiogenous loci are congruent with LSU rDNA sequence analysis of C. virgaureae and Ramularia species. DNA sequences of the type species of both genera, C. virgaureae and R. pusilla, were generated. For the first time a complex cup-shaped appressorium is reported for a member of plant pathogenic cercosporoid hyphomycetes, based on light, scanning and transmission electron microscopy. The appressorium of C. virgaureae is formed by strongly branched hyphae radiating from a supporting intercellular hypha and remaining closely attached to each other. With its concave side the appressorium adheres to a cell of the leaf mesophyll. This structure is significant in comparison with morphologically unspecific intercellular hyphae known in other cercosporoid hyphomycetes. Scanning electron microscopy of conidiogenous loci also provide additional characteristics for distinguishing Cercosporella and Ramularia. Conidiogenous loci are smooth in Cercosporella but similar to the Cladosporium-type (consisting of a circular rim and a central dome) in Ramrnularia.
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