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. 2023 Nov 6;11(11):2717. doi: 10.3390/microorganisms11112717

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© 2023 by the authors.

Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).

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Phylogenetic tree generated from maximum likelihood analysis based on combined ITS, tef1, tub2, cal and his3 sequence data for the Diaporthe arecae species complex and related species. Bootstrap support values for maximum likelihood, maximum parsimony (ML-BS/MP-BS ≥ 70%) and Bayesian posterior probabilities (PP ≥ 0.90) are shown at the nodes. Strains with type status are indicated in bold font. The isolates from this study are presented in brown typeface and the additional isolates from palm tissues included in the analyses are presented in green typeface. Species boundaries within the D. arecae species complex are delimited by colored blocks and their respective branches are indicated by lettered circles (A–C). The scale bar represents the expected number of nucleotide changes per site. The tree is rooted to D. citri (CBS 134239 and CBS 135422).

Phylogenetic tree generated from maximum likelihood analysis based on combined ITS, tef1, tub2, cal and his3 sequence data for the Diaporthe arecae species complex and related species. Bootstrap support values for maximum likelihood, maximum parsimony (ML-BS/MP-BS ≥ 70%) and Bayesian posterior probabilities (PP ≥ 0.90) are shown at the nodes. Strains with type status are indicated in bold font. The isolates from this study are presented in brown typeface and the additional isolates from palm tissues included in the analyses are presented in green typeface. Species boundaries within the D. arecae species complex are delimited by colored blocks and their respective branches are indicated by lettered circles (A–C). The scale bar represents the expected number of nucleotide changes per site. The tree is rooted to D. citri (CBS 134239 and CBS 135422).