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Botryosphaeriaceae associated withPterocarpus angolensis(kiaat) in South Africa

https://doi.org/10.3852/10-003
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/0471650129.dob0522openalex-snapshot
PAUP * [Phylogenetic Analysis Using Parsimony (and Other Methods)]
inferredcites →https://doi.org/10.1007/s11557-009-0622-4openalex-snapshot
Botryosphaeriaceae associated with Terminalia catappa in Cameroon, South Africa and Madagascar
inferredcites →https://doi.org/10.1007/s13225-009-0014-8openalex-snapshot
Endophytic and canker-associated Botryosphaeriaceae occurring on non-native Eucalyptus and native Myrtaceae trees in Uruguay
inferredcites →https://doi.org/10.1016/0168-9525(90)90186-aopenalex-snapshot
PCR protocols — A guide to methods and applications
inferredcites →https://doi.org/10.1016/b978-0-12-372180-8.50042-1openalex-snapshot
AMPLIFICATION AND DIRECT SEQUENCING OF FUNGAL RIBOSOMAL RNA GENES FOR PHYLOGENETICS
inferredcites →https://doi.org/10.1016/j.fbr.2007.06.002openalex-snapshot
Botryosphaeriaceae as endophytes and latent pathogens of woody plants: diversity, ecology and impact
inferredcites →https://doi.org/10.1016/j.foreco.2005.07.004openalex-snapshot
Recruitment of Pterocarpus angolensis in the wild
inferredcites →https://doi.org/10.1016/j.mycres.2006.01.006openalex-snapshot
Two new Fusicoccum species from Acacia and Eucalyptus in Venezuela, based on morphology and DNA sequence data.
inferredcites →https://doi.org/10.1016/j.mycres.2008.11.010openalex-snapshot
Botryosphaeriaceae from tuart (Eucalyptus gomphocephala) woodland, including descriptions of four new species
inferredcites →https://doi.org/10.1016/j.ympev.2007.08.016openalex-snapshot
Phylogeny of the Botryosphaeriaceae reveals patterns of host association
inferredcites →https://doi.org/10.1017/s0953756203007706openalex-snapshot
Multiple gene genealogies and microsatellite markers reflect relationships between morphotypes of Sphaeropsis sapinea and distinguish a new species of Diplodia
inferredcites →https://doi.org/10.1017/s0953756204009748openalex-snapshot
Leptographium wingfieldii introduced into North America and found associated with exotic Tomicus piniperda and native bark beetles
inferredcites →https://doi.org/10.1017/s0953756205003266openalex-snapshot
Seed-borne Botryosphaeria spp. from native Prunus and Podocarpus trees in Ethiopia, with a description of the anamorph Diplodia rosulata sp. nov.
inferredcites →https://doi.org/10.1071/ap08085openalex-snapshot
Pathogenicity of seven species of the Botryosphaeriaceae onEucalyptusclones in Venezuela
inferredcites →https://doi.org/10.1079/dfb/20056400273openalex-snapshot
Diplodia pinea . [Descriptions of Fungi and Bacteria].
inferredcites →https://doi.org/10.1080/00275514.1997.12026785openalex-snapshot
Botryosphaeria mamane sp. nov. associated with witches'-brooms on the endemic forest tree Sophora chrysophylla in Hawaii
inferredcites →https://doi.org/10.1080/00275514.1999.12061051openalex-snapshot
A Method for Designing Primer Sets for Speciation Studies in Filamentous Ascomycetes
inferredcites →https://doi.org/10.1080/00382167.1972.9629277openalex-snapshot
“Trees of Southern Africa”
inferredcites →https://doi.org/10.1080/03610927808827599openalex-snapshot
Further analysis of the data by Akaike's information criterion and the finite corrections
inferredcites →https://doi.org/10.1080/09670877909411658openalex-snapshot
A New Vascular Wilt Disease and its Relationship to Widespread Decline of Pterocarpus angolensis in Zambia
inferredcites →https://doi.org/10.1080/15572536.2005.11832926openalex-snapshot
DNA Phylogeny, Morphology and Pathogenicity of Botryosphaeria Species on Grapevines
inferredcites →https://doi.org/10.1093/bib/bbn013openalex-snapshot
Recent developments in the MAFFT multiple sequence alignment program
inferredcites →https://doi.org/10.1093/bioinformatics/17.8.754openalex-snapshot
MRBAYES: Bayesian inference of phylogenetic trees
inferredcites →https://doi.org/10.1093/molbev/msm092openalex-snapshot
MEGA4: Molecular Evolutionary Genetics Analysis (MEGA) Software Version 4.0
inferredcites →https://doi.org/10.1093/molbev/msn083openalex-snapshot
jModelTest: Phylogenetic Model Averaging
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a026160openalex-snapshot
Markov Chasin Monte Carlo Algorithms for the Bayesian Analysis of Phylogenetic Trees
inferredcites →https://doi.org/10.1094/pdis.2000.84.2.151openalex-snapshot
Characterization of Sphaeropsis sapinea Isolates from South Africa, Mexico, and Indonesia
inferredcites →https://doi.org/10.1094/phyto.2002.92.5.519openalex-snapshot
Characterization of Botryosphaeria dothidea Isolates Collected from Pistachio and Other Plant Hosts in California
inferredcites →https://doi.org/10.1111/j.1365-3059.2006.01486.xopenalex-snapshot
Taxonomy, phylogeny and identification of Botryosphaeriaceae associated with pome and stone fruit trees in South Africa and other regions of the world
inferredcites →https://doi.org/10.1111/j.1365-3059.2007.01608.xopenalex-snapshot
Botryosphaeriaceae occurring on native Syzygium cordatum in South Africa and their potential threat to Eucalyptus
inferredcites →https://doi.org/10.1111/j.1439-0329.2007.00487.xopenalex-snapshot
Diplodia shoot blight and asymptomatic persistence of Diplodia pinea on or in stems of jack pine nursery seedlings
inferredcites →https://doi.org/10.1111/j.1439-0329.2010.00671.xopenalex-snapshot
The pathogenic potential of endophytic Botryosphaeriaceous fungi on Terminalia species in Cameroon
inferredcites →https://doi.org/10.1111/j.1558-5646.1985.tb00420.xopenalex-snapshot
CONFIDENCE LIMITS ON PHYLOGENIES: AN APPROACH USING THE BOOTSTRAP
inferredcites →https://doi.org/10.2307/3761086openalex-snapshot
Botryosphaeria mamane sp. nov. Associated with Witches'-Brooms on the Endemic Forest Tree Sophora chrysophylla in Hawaii
inferredcites →https://doi.org/10.2307/3761991openalex-snapshot
Combined Multiple Gene Genealogies and Phenotypic Characters Differentiate Several Species Previously Identified as Botryosphaeria dothidea
inferredcites →https://doi.org/10.2307/3762177openalex-snapshot
Botryosphaeria corticola, sp. nov. on Quercus Species, with Notes and Description of Botryosphaeria stevensii and Its Anamorph, Diplodia mutila
inferredcites →https://doi.org/10.3114/sim.2009.64.01openalex-snapshot
A class-wide phylogenetic assessment of Dothideomycetes
inferredcites →https://doi.org/10.3114/sim.55.1.235openalex-snapshot
Phylogenetic lineages in the Botryosphaeriaceae
inferredcites →https://doi.org/10.3767/003158508x340742openalex-snapshot
Resolving the phylogenetic and taxonomic status of dark-spored teleomorph genera in the Botryosphaeriaceae
inferredcites →https://doi.org/10.3852/08-020openalex-snapshot
Seven new species of the Botryosphaeriaceae from baobab and other native trees in Western Australia
inferredcites →https://doi.org/10.3852/mycologia.98.3.423openalex-snapshot
Three new Lasiodiplodia spp. from the tropics, recognized based on DNA sequence comparisons and morphology
inferredcites →https://doi.org/10.3852/mycologia.99.5.664openalex-snapshot
Botryosphaeriaceae as potential pathogens of Prunus species in South Africa, with descriptions of Diplodia africana and Lasiodiplodia plurivora sp. nov.
inferredcites →https://doi.org/10.5169/seals-821061openalex-snapshot
Die Gattungen der amerosporen Pyrenomyceten
inferredcites →https://doi.org/10.5281/zenodo.16197769openalex-snapshot
Preliminary studies on the Dothideales in temperate North America

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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First Report of the Sexual Morph of Pseudofusicoccum adansoniae Pavlic, T.I.Burgess & M.J.Wingf. on Para Rubber
inferred← citeshttps://doi.org/10.1007/s10342-019-01200-7openalex-snapshot
Diversity and pathogenicity of Botryosphaeriaceae species on forest trees in the north of Iran
inferred← citeshttps://doi.org/10.1007/s10526-018-09919-9openalex-snapshot
Assessing the potential of fungi isolated from dieback-affected trees as biological control agents for prickly acacia (Vachellia nilotica subsp. indica)
inferred← citeshttps://doi.org/10.1007/s10658-016-0936-4openalex-snapshot
Botryosphaeriaceae species associated with wood diseases of stone and pome fruits trees: symptoms and virulence across different hosts in Uruguay
inferred← citeshttps://doi.org/10.1007/s11557-019-01532-zopenalex-snapshot
Botryosphaerialean fungi causing canker and dieback of tree hosts from Mount Yudu in China
inferred← citeshttps://doi.org/10.1007/s13225-013-0258-1openalex-snapshot
Botryosphaeria, Neofusicoccum, Neoscytalidium and Pseudofusicoccum species associated with mango in Brazil
inferred← citeshttps://doi.org/10.1007/s13225-014-0282-9openalex-snapshot
The complex of Diplodia species associated with Fraxinus and some other woody hosts in Italy and Portugal
inferred← citeshttps://doi.org/10.1007/s13225-014-0285-6openalex-snapshot
Botryosphaeriaceae and Diaporthaceae associated with panicle and shoot blight of pistachio in California, USA
inferred← citeshttps://doi.org/10.1007/s13225-020-00462-6openalex-snapshot
Refined families of Dothideomycetes: orders and families incertae sedis in Dothideomycetes
inferred← citeshttps://doi.org/10.1007/s13225-021-00484-8openalex-snapshot
What is a species in fungal plant pathogens?
inferred← citeshttps://doi.org/10.1007/s13313-014-0284-9openalex-snapshot
Botryosphaeriaceae associated with diseases of mango (Mangifera indica)
inferred← citeshttps://doi.org/10.1007/s13313-017-0516-xopenalex-snapshot
Diversity of tree-infecting Botryosphaeriales on native and non-native trees in South Africa and Namibia
inferred← citeshttps://doi.org/10.1007/s13313-018-0559-7openalex-snapshot
Australian cultures of Botryosphaeriaceae held in Queensland and Victoria plant pathology herbaria revisited
inferred← citeshttps://doi.org/10.1007/s13313-018-0586-4openalex-snapshot
New Botryosphaeriales on native red milkwood (Mimusops caffra)
inferred← citeshttps://doi.org/10.1007/s13314-021-00416-0openalex-snapshot
Pseudofusicoccum sp. causing shoot canker in peach in Uruguay
inferred← citeshttps://doi.org/10.1016/b978-0-12-821008-6.00016-5openalex-snapshot
Bioprospecting for secondary metabolites of family Botryosphaeriaceae from a biotechnological perspective
inferred← citeshttps://doi.org/10.1016/j.bjbas.2018.06.001openalex-snapshot
Mellein, a dihydroisocoumarin with bioherbicidal activity from a new strain of Lasiodiplodia pseudotheobromae C1136
inferred← citeshttps://doi.org/10.1016/j.funbio.2011.12.001openalex-snapshot
High gene flow and outcrossing within populations of two cryptic fungal pathogens on a native and non-native host in Cameroon
inferred← citeshttps://doi.org/10.1016/j.funbio.2013.11.007openalex-snapshot
Botryosphaeriaceae species overlap on four unrelated, native South African hosts
inferred← citeshttps://doi.org/10.1016/j.funbio.2014.04.006openalex-snapshot
Secretome analysis identifies potential virulence factors of Diplodia corticola, a fungal pathogen involved in cork oak (Quercus suber) decline
inferred← citeshttps://doi.org/10.1016/j.funbio.2016.04.005openalex-snapshot
The new family Septorioideaceae, within the Botryosphaeriales and Septorioides strobi as a new species associated with needle defoliation of Pinus strobus in the United States
inferred← citeshttps://doi.org/10.1016/j.funbio.2016.07.015openalex-snapshot
Overlap of latent pathogens in the Botryosphaeriaceae on a native and agricultural host
inferred← citeshttps://doi.org/10.1016/j.funbio.2016.09.004openalex-snapshot
Endophytic Botryosphaeriaceae, including five new species, associated with mangrove trees in South Africa
inferred← citeshttps://doi.org/10.1016/j.funbio.2021.04.006openalex-snapshot
Botryosphaeriaceae on Syzygium cordatum across a latitudinal gradient in South Africa
inferred← citeshttps://doi.org/10.1016/j.funeco.2015.03.001openalex-snapshot
Temporal and spatial variation of Botryosphaeriaceae associated with Acacia karroo in South Africa
inferred← citeshttps://doi.org/10.1016/j.micres.2016.05.004openalex-snapshot
DNA barcoding and isolation of vertically transmitted ascomycetes in sorghum from Burkina Faso: Epicoccum sorghinum is dominant in seedlings and appears as a common root pathogen
inferred← citeshttps://doi.org/10.1016/j.pmpp.2025.102817openalex-snapshot
Diversity of fungal species causing apple canker disease in India using multigene characterization
inferred← citeshttps://doi.org/10.1055/a-1041-3406openalex-snapshot
Scientistsʼ Warning on Climate Change and Medicinal Plants
inferred← citeshttps://doi.org/10.1080/03235408.2012.749703openalex-snapshot
Morphological and molecular characterization of Diplodia seriata , the causal agent of canker and twig dieback disease on mulberry in Iran
inferred← citeshttps://doi.org/10.1094/pdis-05-16-0612-reopenalex-snapshot
Botryosphaeriaceae Species Associated With Cankers and Dieback Symptoms of Acacia mangium and Pinus caribaea var. hondurensis in Venezuela
inferred← citeshttps://doi.org/10.1094/pdis-07-13-0706-reopenalex-snapshot
Phylogeny, Morphology, Distribution, and Pathogenicity of Botryosphaeriaceae and Diaporthaceae from English Walnut in California
inferred← citeshttps://doi.org/10.1111/efp.12116openalex-snapshot
Botryosphaeriaceae associated with die‐back of S chizolobium parahyba trees in S outh A frica and E cuador
inferred← citeshttps://doi.org/10.1111/j.1365-3059.2011.02431.xopenalex-snapshot
Characterization of Botryosphaeriaceae from plantation‐grown Eucalyptus species in South China
inferred← citeshttps://doi.org/10.1111/jam.14828openalex-snapshot
Identification of Botryosphaeriaceae associated with stem‐end rot of mango ( Mangifera indica L.) in Malaysia
inferred← citeshttps://doi.org/10.1111/jph.12384openalex-snapshot
New Records of Lasiodiplodia theobromae in Seeds of Tetrapleura tetraptera from Nigeria and Fruit of Cocos nucifera From Mexico
inferred← citeshttps://doi.org/10.1111/jph.13443openalex-snapshot
Management Strategies for Macadamia Branch Dieback in South Africa
inferred← citeshttps://doi.org/10.15287/afr.2023.2492openalex-snapshot
A review of Botryosphaeriales in Venezuela with special reference to woody plants
inferred← citeshttps://doi.org/10.1590/0100-5405/245874openalex-snapshot
Mycobiota associated with anthracnose and dieback symptoms on Theobroma cacao L. in Mérida State, Venezuela
inferred← citeshttps://doi.org/10.1590/s1982-56762014000600008openalex-snapshot
New occurrences of Botryosphaeriaceae causing black root rot of cassava in Brazil
inferred← citeshttps://doi.org/10.2903/j.efsa.2023.7737openalex-snapshot
Pest categorisation of Lasiodiplodia pseudotheobromae
inferred← citeshttps://doi.org/10.2989/20702620.2010.547244openalex-snapshot
Die-back of kiaat (Pterocarpus angolensis) in southern Africa: a cause for concern?
inferred← citeshttps://doi.org/10.2989/20702620.2011.639499openalex-snapshot
Lasiodiplodiaspecies associated with dyingEuphorbia ingensin South Africa
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Global forest research, science education and community service positively impacted by a unique Centre of Excellence in Tree Health Biotechnology
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Botryosphaeriaceae partially overlap on asymptomatic and symptomatic tissues of Anacardiaceae in agroecosystems and conservation areas in northern South Africa
inferred← citeshttps://doi.org/10.3114/sim0021openalex-snapshot
The Botryosphaeriaceae: genera and species known from culture
inferred← citeshttps://doi.org/10.3390/f13020341openalex-snapshot
Diversity of Endophytes in the Botryosphaeriaceae Differs on Anacardiaceae in Disturbed and Undisturbed Ecosystems in South Africa
inferred← citeshttps://doi.org/10.3390/f8050145openalex-snapshot
Invasive Everywhere? Phylogeographic Analysis of the Globally Distributed Tree Pathogen Lasiodiplodia theobromae
inferred← citeshttps://doi.org/10.3390/pathogens12040574openalex-snapshot
Characterization of Pseudofusicoccum Species from Diseased Plantation-Grown Acacia mangium, Eucalyptus spp., and Pinus massoniana in Southern China
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Resolving the Diplodia complex on apple and other Rosaceae hosts
inferred← citeshttps://doi.org/10.3767/003158514x684780openalex-snapshot
Confronting the constraints of morphological taxonomy in the Botryosphaeriales
inferred← citeshttps://doi.org/10.3767/003158515x685841openalex-snapshot
Caulicolous Botryosphaeriales from Thailand
inferred← citeshttps://doi.org/10.3767/persoonia.2018.40.03openalex-snapshot
Botryosphaeriaceae from Eucalyptus plantations and adjacent plants in China
inferred← citeshttps://doi.org/10.3852/12-107openalex-snapshot
Phylogeny and taxonomy of Botryosphaeria and Neofusicoccum species in Iran, with description of Botryosphaeria scharifii sp. nov.
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A Review of Pterocarpus angolensis DC. (Mukwa) an Important and Threatened Timber Species of the Miombo Woodlands
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Pseudofusicoccum adansoniae isolated as an endophyte from Jatropha podagrica: new record for India
inferred← citeshttps://doi.org/10.5423/ppj.oa.03.2023.0039openalex-snapshot
Identification and Characterization of Diplodia parva and Diplodia crataegicola Causing Black Rot of Chinese Quince
inferred← citeshttps://doi.org/10.5943/mycosphere/14/1/14openalex-snapshot
Lasiodiplodia: Generic revision by providing molecular markers, geographical distribution and haplotype diversity
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ITS-rDNA sequences differentiate a new lineage of Diplodia associated with canker disease of apple in Iran
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Fungal Safari on Palm Trees: New Discoveries from East Asia and Global Records from 1990–2025
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Five New Species of the Botryosphaeriaceae from Acacia Karroo in South Africa
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