Speciation and distribution of Botryosphaeria spp. on native and introduced Eucalyptus trees in Australia and South Africa

By B. Slippers, G. Fourie, P. W. Crous, T. Coutinho, B. Wingfield, A. Carnegie, Michael J. Wingfield. 2004

138 citations recorded by the source corpus.

View Paper: https://www.semanticscholar.org/paper/cd4128f19b6a4465d9a5306a062ef2f795852c81

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Citations in the corpus

Hosts, species and genotypes: opinions versus data (2005, background): “However, a multi-gene phylogeny revealed that isolates obtained from Acacia in Australia were in fact representative of a new species, B. australis (Slippers et al. 2004c).”
Endophytic and canker-associated Botryosphaeriaceae occurring on non-native Eucalyptus and native Myrtaceae trees in Uruguay (2010, methodology): “Using a modern taxonomic concept for Botryosphaeriaceae, B. dothidea has rarely been isolated from Eucalyptus spp. and it has been suggested that this fungus may not be an important pathogen of these trees (Slippers et al. 2004b; Pavlic et al. 2007).”
Diversity of saprobic microfungi (2007, background): “A similar situation exists in Botryosphaeria, where numerous new taxa are being discovered, which seem to have their own host ranges and geographic distributions (Slippers et al. 2004; Crous et al. 2006f; Phillips et al. 2006).”
Botryosphaeriaceae occurring on native Syzygium cordatum in South Africa and their potential threat to Eucalyptus (2007, methodology): “Furthermore, identification of large numbers of species has been facilitated by PCR restriction fragment length polymorphism (RFLP) techniques (Slippers et al 2004b).”
The Botryosphaeriaceae: genera and species known from culture (2013, methodology): “Only after gene sequence data were used to clarify species concepts in the genus (e.g. Phillips et al. 2002, Slippers et al. 2004a) it became apparent that some of the earlier reports of B. dothidea in association with plant diseases may have been misidentifications.”
Established and new technologies reduce increasing pest and pathogen threats to Eucalypt plantations (2013, background): “2b) (Slippers et al., 2004; Barber et al., 2005) and Cryphonectriaceae (Gryzenhout et al., 2006), canker and wilt pathogens such as species of Ceratocystis sensu lato (Van Wyk et al., 2012) leaf and root pathogens such as species of Calonectria (Fig.”
Endophytes as potential pathogens of the baobab species Adansonia gregorii: a focus on the Botryosphaeriaceae (2011, background): “Africa and Australia share a large amount of floral families, such as Myrtaceae and Proteaceae (Beadle 1981), and they also share the pathogens of many of these plants (Crous et al. 2000; Slippers et al. 2004; Slippers et al. 2005a).”
The challenge of understanding the origin, pathways and extent of fungal invasions: global populations of the Neofusicoccum parvum–N. ribis species complex (2013, unknown): “…analysis, ISSR fingerprinting, sequence data and detailed morphological work provided support for the separation of N. ribis and B. dothidea and for the distinction of these two species from N. parvum (Smith & Stanosz, 1997, 2001; Jacobs & Rehner, 1998; Zhou et al., 2001; Slippers et al., 2004b).”
Occurrence and pathogenicity of fungi in necrotic and non-symptomatic shoots of declining common ash (Fraxinus excelsior) in Sweden (2008, background): “stevensii, known as opportunistic pathogen causing similar symptoms on other deciduous trees (Vajna 1986; Luque and Girbal 1989; Slippers et al. 2004), inoculation in each case lead to bark necroses on 2-year-old F.”
AJOM new records and collections of fungi: 1–100 (2020, background): “…– Actinidia deliciosa, Heteropyxis natalensis, Malus sylvestris, Populus nigra, Eucalyptus sp., E. grandis, E. smithii, Ribes sp., Sequoia gigantea (Slippers et al. 2004), Acer pseudoplatanus, Quercus robur (Moricca et al. 2012), Actinidia deliciosa, A. chinensis, Populus nigra, Eucalyptus…”
Taxonomy, phylogeny and identification of Botryosphaeriaceae associated with pome and stone fruit trees in South Africa and other regions of the world (2007, methodology): “…represented either N. australe, N. ribis or N. parvum, because the conidial features reported in the studies above overlap with the morphology of all these last named species (Putterill, 1919; Combrink et al., 1984; Pennycook & Samuels, 1985; Phillips et al., 2002; Slippers et al., 2004a,c).”