The Botryosphaeriaceae: genera and species known from culture
By A. Phillips, A. Alves, J. Abdollahzadeh, B. Slippers, Michael J. Wingfield, Johannes Z. Groenewald, P. W. Crous. Studies in Mycology, 2013
865 citations recorded by the source corpus.
In this paper we give an account of the genera and species in the Botryosphaeriaceae. We consider morphological characters alone as inadequate to define genera or identify species, given the confusion it has repeatedly introduced in the past, their variation during development, and inevitable overlap as representation grows. Thus it seems likely that all of the older taxa linked to the Botryosphaeriaceae, and for which cultures or DNA sequence data are not available, cannot be linked to the species in this family that are known from culture. Such older taxa will have to be disregarded for future use unless they are epitypified. We therefore focus this paper on the 17 genera that can now be recognised phylogenetically, which concentrates on the species that are presently known from culture. Included is a historical overview of the family, the morphological features that define the genera and species and detailed descriptions of the 17 genera and 110 species. Keys to the genera and species are also provided. Phylogenetic relationships of the genera are given in a multi-locus tree based on combined SSU, ITS, LSU, EF1-α and β-tubulin sequences. The morphological descriptions are supplemented by phylogenetic trees (ITS alone or ITS + EF1-α) for the species in each genus. Taxonomic novelties: New species - Neofusicoccum batangarum Begoude, Jol. Roux & Slippers. New combinations - Botryosphaeria fabicerciana (S.F. Chen, D. Pavlic, M.J. Wingf. & X.D. Zhou) A.J.L. Phillips & A. Alves, Botryosphaeria ramosa (Pavlic, T.I. Burgess, M.J. Wingf.) A.J.L. Phillips & A. Alves, Cophinforma atrovirens (Mehl & Slippers) A. Alves & A.J.L. Phillips, Cophinforma mamane (D.E. Gardner) A.J.L. Phillips & A. Alves, Dothiorella pretoriensis (Jami, Gryzenh., Slippers & M.J. Wingf.) Abdollahz. & A.J.L. Phillips, Dothiorella thailandica (D.Q. Dai., J.K. Liu & K.D. Hyde) Abdollahz., A.J.L. Phillips & A. Alves, Dothiorella uruguayensis (C.A. Pérez, Blanchette, Slippers & M.J. Wingf.) Abdollahz. & A.J.L. Phillips, Lasiodiplodia lignicola (Ariyawansa, J.K. Liu & K.D. Hyde) A.J.L. Phillips, A. Alves & Abdollahz., Neoscytalidium hyalinum (C.K. Campb. & J.L. Mulder) A.J.L. Phillips, Groenewald & Crous, Sphaeropsis citrigena (A.J.L. Phillips, P.R. Johnst. & Pennycook) A.J.L. Phillips & A. Alves, Sphaeropsis eucalypticola (Doilom, J.K. Liu, & K.D. Hyde) A.J.L. Phillips, Sphaeropsis porosa (Van Niekerk & Crous) A.J.L. Phillips & A. Alves. Epitypification (basionym) - Sphaeria sapinea Fries. Neotypifications (basionyms) - Botryodiplodia theobromae Pat., Physalospora agaves Henn, Sphaeria atrovirens var. visci Alb. & Schwein.
Subfields: Biomedical Engineering, Cell Biology, Plant Science
View Paper: https://www.semanticscholar.org/paper/1ad818712475184ca9635856e8cbb8746364d585
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In Biomedical Engineering
In Cell Biology
- K. D. Hyde
- M. Dayarathne
- Asha J. Dissanayake
- E. McKenzie
- D. Bhat
- Jiankui Liu
- R. Jeewon
- Ali H. Bahkali
In Plant Science
- K. D. Hyde
- M. Dayarathne
- Asha J. Dissanayake
- E. McKenzie
- D. Bhat
- Jiankui Liu
- R. Jeewon
- Ali H. Bahkali
Citations in the corpus
- Characterisation and pathogenicity of fungal species associated with branch cankers and stem-end rot of avocado in Italy (2016, methodology): “This fungus was recovered from all orchards sampled and was identified by comparing morphology and through phylogenetic analysis (Phillips et al. 2013).”
- Microfungi on Tectona grandis (teak) in Northern Thailand (2016, methodology): “Botryosphaeriaceae currently consists of 17 genera based on multi-gene phylogenetic analyses and morphology (Phillips et al. 2013; Slippers et al. 2013).”
- What Do We Know about Botryosphaeriaceae? An Overview of a Worldwide Cured Dataset (2021, background): “Therefore, over the years the taxonomic position of these organisms suffered multiple classifications (for a historical overview, see [1]).”
- Morpho-molecular characterization of microfungi associated with marine based habitats (2020, background): “…agents of disease on ecologically and economically important plants (Slippers & Wingfield 2007, Mehl et al. 2014, Tibpromma et al. 2018) and cosmopolitan in distribution but absent in polar regions (Hyde et al. 2013, 2014, Phillips et al. 2013, 2019, Slippers et al. 2013, Dissanayake et al. 2016).”
- One stop shop: backbones trees for important phytopathogenic genera: I (2014) (2014, background): “Based on combined ITS and TEF sequence data seven species are currently recognised in Botryosphaeria (Phillips et al. 2013).”
- Fungal diversity notes 709–839: taxonomic and phylogenetic contributions to fungal taxa with an emphasis on fungi on Rosaceae (2018, background): “Phillips et al. (2013) and Slippers et al. (2014) have shown that morphology is not a reliable character for species differentiation and species can only be recognized from combined ITS and tef1-a sequence data.”
- Fungal diversity notes 491–602: taxonomic and phylogenetic contributions to fungal taxa (2017, background): “Botryosphaeriales is a diverse order with a worldwide distribution, comprising species that vary from endophytes to pathogens (Slippers and Wingfield 2007; Phillips et al. 2013; Chethana et al. 2016; Daranagama et al. 2016; Dissanayake et al. 2016; Giambra et al. 2016; Konta et al. 2016a, b; Linalde”
- Applied aspects of methods to infer phylogenetic relationships amongst fungi (2020, background): “…of both morphology and molecular data developed a more trustworthy and natural classification structure that reveals true phylogenetic associations (Jeewon et al. 2002, 2003, Hyde et al. 2013, Phillips et al. 2013, 2019, Wijayawardene et al. 2014, 2016, 2020, Maharachchikumbura et al. 2015, 2016).”
- What is a species in fungal plant pathogens? (2021, background): “Common examples are Calonectria (sexual) and Cylindrocladium (asexual), Elsinoe (sexual) with Sphaceloma (asexual), Gibberella (sexual) and Fusarium (asexual) morph, Glomerella (sexual) and Colletotrichum (asexual) and the families Botryosphaeriaceae and Mycosphaerellaceae with a large number of ver”