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Catenulostroma chromoblastomycosum (type material). A. Sporodochium on pine needle in vitro . B–H. Chains of disarticulating conidia. Scale bars: A = 350, B, E, G, H = 10 μm. 

Catenulostroma chromoblastomycosum (type material). A. Sporodochium on pine needle in vitro . B–H. Chains of disarticulating conidia. Scale bars: A = 350, B, E, G, H = 10 μm. 

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Mycosphaerella, one of the largest genera of ascomycetes, encompasses several thousand species and has anamorphs residing in more than 30 form genera. Although previous phylogenetic studies based on the ITS rDNA locus supported the monophyly of the genus, DNA sequence data derived from the LSU gene distinguish several clades and families in what ha...

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... chromoblastomycosum Crous & U. Braun, sp. nov. MycoBank MB504505. Fig. 6. Etymology : Named after the disease symptoms observed due to opportunistic human infection. Description based on cultures sporulating on WA supplemented with sterile pine needles. Mycelium consisting of branched, septate, smooth to finely verruculose, medium to dark brown, thick-walled, 3–4 μm wide hyphae. Conidiomata brown, ...

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... The generic concepts of asexual fungi are still based on morphological characters and numerous changes are to be expected in the future. Just as in fungi with other lifestyles, phylogenetic studies have proved that many genera are polyphyletic (Verkley & Starink-Willemse 2004, Crous et al. 2007). The biology and ways of interaction of lichenicolous fungi with their hosts are still rather poorly known, although some anatomic studies have been carried out. ...
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... Once the typical symptoms of gray rot appeared, the fungus was identified by comparing the morphological structures observed (mycelium type and color, septation, conidiophores, conidiophore branching, conidia length and width) using the Barnett and Hunter keys (1998). The specialized descriptions by Ellis (1971) and Crous et al. (2007) were used to determine the species. Samples of the fungus were also sent to the Laboratory of Phytosanitary Diagnosis of Colegio de Postgraduados, Montecillo, Mexico, where they were molecularly analyzed. ...
... En dichas heridas se depositaron 20 µL de una suspensión de 1×10 6 conidios por mililitro. Una vez que se observaron los síntomas típicos de pudrición gris, se procedió a la identificación del hongo comparando las estructuras morfológicas observadas (tipo y color de micelio, septación, conidióforos, ramificación de conidióforos, largo y ancho de conidios) con las claves de Barnett y Hunter (1998); mientras que para la determinación de la especie se emplearon las descripciones especializadas de Ellis (1971) y Crous et al. (2007). Adicionalmente, se enviaron muestras del hongo al Laboratorio de Diagnostico Fitosanitario del Colegio de Postgraduados, Montecillo, México, en donde se analizaron molecularmente. ...
... Once the typical symptoms of gray rot appeared, the fungus was identified by comparing the morphological structures observed (mycelium type and color, septation, conidiophores, conidiophore branching, conidia length and width) using the Barnett and Hunter keys (1998). The specialized descriptions by Ellis (1971) andCrous et al. (2007)were used to determine the species. Samples of the fungus were also sent to the Laboratory of Phytosanitary Diagnosis of Colegio de Postgraduados, Montecillo, Mexico, where they were molecularly analyzed. ...
... En dichas heridas se depositaron 20 µL de una suspensión de 1×10 6 conidios por mililitro. Una vez que se observaron los síntomas típicos de pudrición gris, se procedió a la identificación del hongo comparando las estructuras morfológicas observadas (tipo y color de micelio, septación, conidióforos, ramificación de conidióforos, largo y ancho de conidios) con las claves de Barnett y Hunter (1998); mientras que para la determinación de la especie se emplearon las descripciones especializadas de Ellis (1971) yCrous et al. (2007). Adicionalmente, se enviaron muestras del hongo al Laboratorio de Diagnostico Fitosanitario del Colegio de Postgraduados, Montecillo, México, en donde se analizaron molecularmente. ...
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... Nevertheless, some recent studies have revealed that fungal diseases have a greater impact than was originally suspected.Since the 1990s Mycosphaerella leaf disease (MLD) has been found causing severe defoliation in young trees (Fig. 5.13). WhenCrous et al. (2007)showed that Mycosphaerella is polyphyletic, they transferred many of the species associated with MLD to Teratosphaeria. However, some species, even though phyloge-netically they belong in Teratosphaeria, have not yet been formally transferred and continue to be known by their name in Mycosphaerella.The first report of Mycosphaerella on eucalypts outside of Australia was when von Thümen described M. molleriana (T. ...
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... isolated from historical marble monuments in Anthalia, Turkey (Sert & Sterflinger 2010). If the most conspicuous portion of RIF from natural rocks pooled in the Teratosphaeriaceae, Capnodiales (Crous et al. 2007), a different trend is visible on monuments, as well as coastal sites, where chaetothyrialean fungi predominate. Black fungi in this order are known for their ability to metabolize aromatic compounds (Prenafeta-Boldú et al. 2006; Isola et al. 2013a) and dominate in locations with higher presence of pollutants due to human activities (Onofri et al. 2011). ...
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... More than 150 species of Mycosphaerellaceae and Teratosphaeriaceae have been identified causing diseases in Eucalyptus (Burgess et al. 2007;Crous et al. 2007;Andjic et al. 2010;Carnegie et al. 2011;Hunter et al. 2011), being collectively referred to as Mycosphaerella leaf disease (MLD). Teratosphaeria nubilosa is considered one of the most destructive MLD species worldwide (Mohammed et al. 2003;Hunter et al. 2009). ...
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Since the first report of Teratosphaeria nubilosa (Cooke) Crous & U.Braun in Uruguay in 2007, young plantations of Eucalyptus globulus Labill. and E. maidenii F.Muell. have been severely damaged by Mycosphaerella leaf disease. The genetic variation in disease resistance and in the timing of heteroblastic phase change was examined in 194 openpollinated families of E. globulus and 86 families of E. maidenii growing in a field trial in south-eastern Uruguay, naturally infected by T. nubilosa. Disease severity, precocity of vegetative phase change and tree growth were assessed at 14 months. E. globulus was significantly more susceptible to T. nubilosa than was E. maidenii, presenting higher severity of leaf spots (10.6% and 5.6%, respectively), higher defoliation (31.9% and 22.9%, respectively) and higher crown-damage index (39.1% and 27.4%, respectively). However, the heteroblastic transition began significantly earlier in E. globulus than in E. maidenii, with 34.1% and 2.8% of the trees having some proportion of their crown with adult foliage at 14 months, respectively. Significant individual narrow-sense heritabilities were found in E. globulus for severity of leaf spots (0.40), defoliation (0.24), crown-damage index (0.30) and proportion of adult foliage (0.64). Additive genetic variation in E. maidenii was significant only for defoliation and crown-damage index, with a moderate heritability (0.21 and 0.20, respectively). Although E. maidenii was more resistant to T. nubilosa than was E. globulus, the degree of resistance was not enough to consider this species as an alternative to E. globulus for high-risk disease sites. In addition, the small genetic variability for resistance on the juvenile foliage and the late transition to adult foliage suggested that the chances for early selection in E. maidenii are quite limited. By contrast, the genetic variation in E. globulus clearly indicated that through selection for resistance of the juvenile foliage, and especially by selecting for early phase change, it is possible to obtain genetic stock suitable for sites with high risk of T. nubilosa infection.
... Methods and materials was the same as described by Abbas et al., (2010). Identification up to species level were carried out after consulting (Ellis, 1971Ellis, , 1976 Carmichael et al., 1980; Sutton & Ganapathi, 1978; Ahmad et al., 1997; Kirk, 2012; Crous et al., 2007). ...
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Indirect genetic effects ( IGE s) are heritable effects of individuals on trait values of their conspecifics. IGE s may substantially affect response to selection, but empirical studies on IGE s are sparse and their magnitude and correlation with direct genetic effects are largely unknown in plants. Here we used linear mixed models to estimate genetic (co)variances attributable to direct and indirect effects for growth and foliar disease damage in a large pedigreed population of E ucalyptus globulus . We found significant IGE s for growth and disease damage, which increased with age for growth. The correlation between direct and indirect genetic effects was highly negative for growth, but highly positive for disease damage, consistent with neighbour competition and infection, respectively. IGE s increased heritable variation by 71% for disease damage, but reduced heritable variation by 85% for growth, leaving nonsignificant heritable variation for later age growth. Thus, IGE s are likely to prevent response to selection in growth, despite a considerable ordinary heritability. IGE s change our perspective on the genetic architecture and potential response to selection. Depending on the correlation between direct and indirect genetic effects, IGE s may enhance or diminish the response to natural or artificial selection compared with that predicted from ordinary heritability.
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... Teratosphaeria) and 18 associated anamorph species occurring on Proteaceae. Since this date, however, numerous additional species have been described from this host family (Crous et al. 2007aCrous et al. , 2008Crous et al. , 2009b). Species of Teratosphaeria are commonly associated with leaf spots and blotches on Proteaceae, though not much is known about their host specificity (Crous & Groenewald 2005). ...
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Species of Leucadendron, Leucospermum and Protea (Proteaceae) are in high demand for the international floriculture market due to their brightly coloured and textured flowers or bracts. Fungal pathogens, however, create a serious problem in cultivating flawless blooms. The aim of the present study was to characterise several of these pathogens using morphology, culture characteristics, and DNA sequence data of the rRNA-ITS and LSU genes. In some cases additional genes such as TEF 1-α and CHS were also sequenced. Based on the results of this study, several novel species and genera are described. Brunneosphaerella leaf blight is shown to be caused by three species, namely B. jonkershoekensis on Protea repens, B. nitidae sp. nov. on Protea nitida and B. protearum on a wide host range of Protea spp. (South Africa). Coniothyrium-like species associated with Coniothyrium leaf spot are allocated to other genera, namely Curreya grandicipis on Protea grandiceps, and Microsphaeropsis proteae on P. nitida (South Africa). Diaporthe leucospermi is described on Leucospermum sp. (Australia), and Diplodina microsperma newly reported on Protea sp. (New Zealand). Pyrenophora blight is caused by a novel species, Pyrenophora leucospermi, and not Drechslera biseptata or D. dematoidea as previously reported. Fusicladium proteae is described on Protea sp. (South Africa), Pestalotiopsis protearum on Leucospermum cuneiforme (Zimbabwe), Ramularia vizellae and R. stellenboschensis on Protea spp. (South Africa), and Teratosphaeria capensis on Protea spp. (Portugal, South Africa). Aureobasidium leaf spot is shown to be caused by two species, namely A. proteae comb. nov. on Protea spp. (South Africa), and A. leucospermi sp. nov. on Leucospermum spp. (Indonesia, Portugal, South Africa). Novel genera and species elucidated in this study include Gordonomyces mucovaginatus and Pseudopassalora gouriqua (hyphomycetes), and Xenoconiothyrium catenata (coelomycete), all on Protea spp. (South Africa).