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Symptoms of Eucalyptus rust on different hosts. a Young lesions on E. grandis, the pustules are bright orange on young tissue. b Old lesions on E. grandis, grey discoloration on leaves and twigs and dead shoot tip. c,d Pustules on twigs, leaves and petioles of Myrrhinium atropurpureum var. octandrum appear bright orange. Trees also have dead shoot tips. Arrows show areas of dying shoot tips and location of orange urediniospores on infected branches.  

Symptoms of Eucalyptus rust on different hosts. a Young lesions on E. grandis, the pustules are bright orange on young tissue. b Old lesions on E. grandis, grey discoloration on leaves and twigs and dead shoot tip. c,d Pustules on twigs, leaves and petioles of Myrrhinium atropurpureum var. octandrum appear bright orange. Trees also have dead shoot tips. Arrows show areas of dying shoot tips and location of orange urediniospores on infected branches.  

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Eucalyptus or guava rust caused by Puccinia psidii is a serious disease of Eucalyptus and other Myrtaceae. In Uruguay, it has been previously found on Eucalyptus globulus and Psidium brasiliensis. Almost nothing is known regarding the occurrence of this pathogen on other Eucalyptus species or native Myrtaceae in that country. In this study, we dete...

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... symptoms were observed on different hosts infected with P. psidii. Lesions were primarily observed on young tissues such as actively growing leaves and shoots (Fig. 1). Bright orange pustules with orange-yellow urediniospores were present on all evaluated hosts, but dark orange- brown teliospores were observed only on E. globulus and E. grandis. Gray discoloration of old lesions was observed on E. grandis, and shoot tips were dead on E. grandis and M. atropurpureum var. octandrum (Fig. 1). ...
Context 2
... leaves and shoots (Fig. 1). Bright orange pustules with orange-yellow urediniospores were present on all evaluated hosts, but dark orange- brown teliospores were observed only on E. globulus and E. grandis. Gray discoloration of old lesions was observed on E. grandis, and shoot tips were dead on E. grandis and M. atropurpureum var. octandrum (Fig. 1). Teliospores were similar to those reported by Walker (1983), roughly ellipsoidal to cylindrical to broadly clavate, one-septate, constricted at the central septum, 26-42 × 15-22 μm, with the upper cell generally slightly wider and shorter than the lower, wall pale golden yellow, pore apical in the upper cell and just below the septum ...

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... Host shifts. The negative impact of host-jump events from commercial settings to native forest ecosystems, and vice versa, has been recorded in the region [28,[51][52][53]. Funding to research native forest ecosystems is scarce in the region. ...
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... Eucalyptus citriodora; Joffily, 1944). Considered to be of neotropical origin, the pathogen has also been reported to infect other diverse myrtaceous hosts in South America (e.g., Granados et al., 2017;Kern & Toro, 1935;Mohali & Aime, 2016;Pérez, Wingfield, Altier, Simeto, & Blanchette, 2011;Simpson, Thomas, & Grgurinovic, 2006;Tommerup, Alfenas, & Old, 2003), the Caribbean (MacLachlan, 1938), California, USA (Mellano, 2006;Zambino & Nolan, 2011), Florida, USA (Marlatt & Kimbrough, 1979), Hawaii, USA (Uchida, Zhong, & Kilgore, 2006), Japan (Kawanishi et al., 2009), Australia (Carnegie et al., 2010), Hainan, China (Zhuang & Wei, 2011), and most recently South Africa (Roux, Greyling, Coutinho, Verleur, & Wingfield, 2013), New Caledonia (Giblin, 2013), Indonesia (McTaggart et al., 2016) and Singapore (de Plessis et al., 2017). In addition to rapid global spread of the myrtle rust pathogen in recent years, emergent natural epiphytotics (e.g., Rayachhetry, Elliott, & Van, 1997;Rayamajhi, Pratt, Klopfenstein, Ross-Davis, & Rodgers, 2013;Uchida & Loope, 2009) and new host reports (e.g., Pérez et al., 2011;Rodas et al., 2015;Telechea, Rolfo, Coutinho, & Wingfield, 2003;Zambino & Nolan, 2011) continue to be observed and documented within the Americas and Hawaii. ...
... Considered to be of neotropical origin, the pathogen has also been reported to infect other diverse myrtaceous hosts in South America (e.g., Granados et al., 2017;Kern & Toro, 1935;Mohali & Aime, 2016;Pérez, Wingfield, Altier, Simeto, & Blanchette, 2011;Simpson, Thomas, & Grgurinovic, 2006;Tommerup, Alfenas, & Old, 2003), the Caribbean (MacLachlan, 1938), California, USA (Mellano, 2006;Zambino & Nolan, 2011), Florida, USA (Marlatt & Kimbrough, 1979), Hawaii, USA (Uchida, Zhong, & Kilgore, 2006), Japan (Kawanishi et al., 2009), Australia (Carnegie et al., 2010), Hainan, China (Zhuang & Wei, 2011), and most recently South Africa (Roux, Greyling, Coutinho, Verleur, & Wingfield, 2013), New Caledonia (Giblin, 2013), Indonesia (McTaggart et al., 2016) and Singapore (de Plessis et al., 2017). In addition to rapid global spread of the myrtle rust pathogen in recent years, emergent natural epiphytotics (e.g., Rayachhetry, Elliott, & Van, 1997;Rayamajhi, Pratt, Klopfenstein, Ross-Davis, & Rodgers, 2013;Uchida & Loope, 2009) and new host reports (e.g., Pérez et al., 2011;Rodas et al., 2015;Telechea, Rolfo, Coutinho, & Wingfield, 2003;Zambino & Nolan, 2011) continue to be observed and documented within the Americas and Hawaii. ...
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Since the myrtle rust pathogen (Austropuccinia psidii) was first reported (as Puccinia psidii) in Brazil on guava (Psidium guajava) in 1884, it has been found infecting diverse myrtaceous species. Because A. psidii has recently spread rapidly worldwide with an extensive host range, genetic and genotypic diversities were evaluated within and among A. psidii populations in its putative native range and other areas of myrtle rust emergence in the Americas and Hawaii. Microsatellite markers revealed several unique multilocus genotypes (MLGs), which grouped isolates into nine distinct genetic clusters [C1–C9 comprising C1: from diverse hosts from Costa Rica, Jamaica, Mexico, Puerto Rico, and USA-Hawaii, and USA-California; C2: from eucalypts (Eucalyptus spp.) in Brazil/Uruguay and rose apple (Syzygium jambos) in Brazil; C3: from eucalypts in Brazil; C4: from diverse hosts in USA-Florida; C5: from Java plum (Syzygium cumini) in Brazil; C6: from guava and Brazilian guava (Psidium guineense) in Brazil; C7: from pitanga (Eugenia uniflora) in Brazil; C8: from allspice (Pimenta dioica) in Jamaica and sweet flower (Myrrhinium atropurpureum) in Uruguay; C9: from jabuticaba (Myrciaria cauliflora) in Brazil]. The C1 cluster, which included a single MLG infecting diverse host in many geographic regions, and the closely related C4 cluster are considered as a “Pandemic biotype,” associated with myrtle rust emergence in Central America, the Caribbean, USA-Florida, USA-Hawaii, Australia, China-Hainan, New Caledonia, Indonesia and Colombia. Based on 19 bioclimatic variables and documented occurrences of A. psidii contrasted with reduced sets of specific genetic clusters (subnetworks, considered as biotypes), maximum entropy bioclimatic modelling was used to predict geographic locations with suitable climate for A. psidii which are at risk from invasion. The genetic diversity of A. psidii throughout the Americas and Hawaii demonstrates the importance of recognizing biotypes when assessing the invasive threats posed by A. psidii around the globe.
... In addition, this disease has been reported in many parts of the world such as the United States (Marlatt & Kimbrough, 1979;Mellano, 2006;Rayachhetry, Elliot, & Van, 1997;Uchida, Zhong, & Killgore, 2006;Zambino & Nolan, 2011), Mexico (Gallegos & Cummins, 1981), Japan (Kawanishi et al., 2009), Australia (Carnegie et al., 2010), China (Zhuang & Wei, 2011), South Africa (Roux, Greyling, Coutinho, Verleur, & Wingfield, 2013), New Caledonia (Giblin, 2013), Colombia (Rodas et al., 2015) and Indonesia . This global spread of P. psidii is indicative that phytosanitary measures are required to control its movement, especially in the tropical and subtropical regions where its occurrence and severity are more intense, as reported by recent studies in Uruguay (Pérez, Wingfield, Altier, Simeto, & Blanchette, 2011) and Brazil . ...
Article
Brazilian forest-based industries are supported by more than 5.5 million hectares of Eucalyptus growing under different climatic conditions with different degrees of favourability for rust Puccinia psidii, including both traditional and expanding areas, where such disease is of major concern for the industry, foresters and scientists. The main objective of this study was to define favourable climatic zones for Eucalyptus rust in Brazil with the following aims: (i) to develop a spatial method for estimating the mean night-time temperature (Tng); (ii) to assess and validate a Eucalyptus rust model; and (iii) to map Eucalyptus rust favourability zones in Brazil based on the proposed model. A straightforward method, based only on latitude, day of the year, maximum and minimum air temperatures, was developed to estimate Tng, which is a key variable for a proper application of Ruiz rust model. Based on 37 field experiments with natural rust occurrence, it was observed that climatic conditions are determining factors for disease severity. Significant correlations between disease severity observed in the field and climatic conditions were found: a negative correlation with temperature (r = .50, p < .01) and a positive correlation with relative humidity (r = .89, p < .0001). A significant correlation (r = .81, p < .0001) between the normalized infection index, produced from Ruiz model, and the average rust score was also observed. Once the model was validated under field conditions, it was applied using historical average data of air temperature and leaf wetness duration to obtain monthly Eucalyptus rust favourability maps for the whole country. These final maps show that favourable climatic zones for Eucalyptus rust are extremely dynamic, with high temporal and spatial variability in Brazil and that climatic conditions should be considered for expansion of Eucalyptus to new areas, in breeding programmes, and for defining the most suitable seasons for forest establishment in each climate of the country. These results provide forestry managers with practical tools to reduce uncertainty about the expected severity of Eucalyptus rust in Brazil.