<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>46</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Australian Department of the Environment</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Environment Protection and Biodiversity Conservation Act 1999</style></title></titles><dates><year><style  face="normal" font="default" size="100%">1999</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://www.environment.gov.au/biodiversity/invasive/diseases/phytophthora-cinnamomi.html</style></url></web-urls></urls><isbn><style face="normal" font="default" size="100%">0 642 24863 3</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">C.M. Brasier</style></author><author><style face="normal" font="default" size="100%">Robredo, F.</style></author><author><style face="normal" font="default" size="100%">Ferraz, J. F. P.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Evidence for Phytophthora cinnamomi involvement in Iberian oak decline</style></title><secondary-title><style face="normal" font="default" size="100%">Plant Pathology</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">1993</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1111/j.1365-3059.1993.tb01482.x</style></url></web-urls></urls><number><style face="normal" font="default" size="100%">1</style></number><publisher><style face="normal" font="default" size="100%">Blackwell Publishing Ltd</style></publisher><volume><style face="normal" font="default" size="100%">42</style></volume><pages><style face="normal" font="default" size="100%">140–145</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Rapid and sometimes extensive mortality and decline of oak, principally &lt;em&gt;Quercus suber&lt;/em&gt; and &lt;em&gt;Q. ilex&lt;/em&gt;, has occurred in parts of southern Spain and Portugal in recent decades. We report here isolation of the aggressive root pathogen &lt;em&gt;Phytophthora cinnamomi&lt;/em&gt; from roots of diseased oaks or from soil at eleven out of thirteen decline foci examined. It is proposed that the introduction and spread of &lt;em&gt;P. cinnamomi&lt;/em&gt; may be a major factor in the Iberian oak decline, interacting with drought and other site factors, and leading to stress-related attacks by insects and other fungi. By analogy, it may also be involved in the similar oak declines occurring elsewhere on the Mediterranean.&lt;/p&gt;</style></abstract></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Chandelier, A.</style></author><author><style face="normal" font="default" size="100%">Abras, S.</style></author><author><style face="normal" font="default" size="100%">Laurent, F.</style></author><author><style face="normal" font="default" size="100%">Debruxelles, N.</style></author><author><style face="normal" font="default" size="100%">Cavelier, M.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Effect of temperature and bacteria on sporulation of Phytophthora alni in river water</style></title><secondary-title><style face="normal" font="default" size="100%">Commun Agric Appl Biol Sci.</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2006</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://www.ncbi.nlm.nih.gov/pubmed/17390834</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">71</style></volume><pages><style face="normal" font="default" size="100%">873–80</style></pages><language><style face="normal" font="default" size="100%">eng</style></language></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">De Dobbelaere, I.</style></author><author><style face="normal" font="default" size="100%">Vercauteren, A.</style></author><author><style face="normal" font="default" size="100%">Speybroeck, N.</style></author><author><style face="normal" font="default" size="100%">Berkvens, D.</style></author><author><style face="normal" font="default" size="100%">Van Bockstaele, E.</style></author><author><style face="normal" font="default" size="100%">Maes, M.</style></author><author><style face="normal" font="default" size="100%">Heungens, K.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Effect of host factors on the susceptibility of Rhododendron to Phytophthora ramorum</style></title><secondary-title><style face="normal" font="default" size="100%">Plant Pathology</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">host resistance</style></keyword><keyword><style  face="normal" font="default" size="100%">leaf age</style></keyword><keyword><style  face="normal" font="default" size="100%">leaf hairs</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytophthora kernoviae</style></keyword><keyword><style  face="normal" font="default" size="100%">rootstock</style></keyword><keyword><style  face="normal" font="default" size="100%">sporulation</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2010</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1111/j.1365-3059.2009.02212.x</style></url></web-urls></urls><number><style face="normal" font="default" size="100%">2</style></number><publisher><style face="normal" font="default" size="100%">Blackwell Publishing Ltd</style></publisher><volume><style face="normal" font="default" size="100%">59</style></volume><pages><style face="normal" font="default" size="100%">301–312</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;&lt;em&gt;Phytophthora ramorum&lt;/em&gt; causes sudden oak death (SOD) in western coastal forests of the USA. In Europe, the pathogen is mainly present in the nursery industry, particularly on &lt;em&gt;Rhododendron.&lt;/em&gt; Because of the primary role of &lt;em&gt;Rhododendron&lt;/em&gt; as a host and potentially as a vector, the effect of &lt;em&gt;Rhododendron&lt;/em&gt; host factors on &lt;em&gt;P. ramorum&lt;/em&gt; susceptibility and sporulation was investigated. Inoculation methods using either wounded or non-wounded detached leaves were applied to 59 &lt;em&gt;Rhododendron&lt;/em&gt; cultivars and 22 botanical species, replicated in three separate years. All &lt;em&gt;Rhododendron&lt;/em&gt; species and cultivars were susceptible when using wounded leaves, but not when using non-wounded leaves, suggesting a resistance mechanism operating at the level of leaf penetration. Using a regression tree analysis, the cultivars and species were split into four susceptibility classes. Young leaves were more susceptible than mature leaves when wounded, but less susceptible when non-wounded. This effect was not correlated with leaf hydrophobicity or the number of leaf hairs. The presence or the type of rootstock did not affect the cultivar susceptibility level. Sporangia and chlamydospore production in the leaf lesions varied widely among &lt;em&gt;Rhododendron&lt;/em&gt; cultivars and was not correlated with the susceptibility level. The susceptibility to &lt;em&gt;P. ramorum&lt;/em&gt; correlated well with the susceptibility to &lt;em&gt;P. citricola&lt;/em&gt; and &lt;em&gt;P. hedraiandra&amp;nbsp;&lt;/em&gt;×&lt;em&gt;&amp;nbsp;cactorum&lt;/em&gt;, suggesting that the resistance mechanisms against these species are non-specific. Susceptibility to &lt;em&gt;P. kernoviae&lt;/em&gt; was low for most cultivars. These findings have implications for detection, spread and disease control, and are therefore important in pest risk assessment.&lt;/p&gt;</style></abstract></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Richard S. Dodd</style></author><author><style face="normal" font="default" size="100%">Hüberli, , Daniel</style></author><author><style face="normal" font="default" size="100%">Mayer, Wasima</style></author><author><style face="normal" font="default" size="100%">Harnik, Tamar Y.</style></author><author><style face="normal" font="default" size="100%">Afzal-Rafii, Zara</style></author><author><style face="normal" font="default" size="100%">Garbelotto, Matteo</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Evidence for the role of synchronicity between host phenology and pathogen activity in the distribution of sudden oak death canker disease</style></title><secondary-title><style face="normal" font="default" size="100%">New Phytologist</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">exotic pathogen</style></keyword><keyword><style  face="normal" font="default" size="100%">inoculation</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytophthora ramorum</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus agrifolia</style></keyword><keyword><style  face="normal" font="default" size="100%">resistance</style></keyword><keyword><style  face="normal" font="default" size="100%">spatial distribution</style></keyword><keyword><style  face="normal" font="default" size="100%">synchronicity</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2008</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1111/j.1469-8137.2008.02450.x</style></url></web-urls></urls><number><style face="normal" font="default" size="100%">2</style></number><publisher><style face="normal" font="default" size="100%">Blackwell Publishing Ltd</style></publisher><volume><style face="normal" font="default" size="100%">179</style></volume><pages><style face="normal" font="default" size="100%">505–514</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Variations in synchronicity between colonization rate by the pathogen and host phenology may account for unexplained spatial distribution of canker disease. The hypothesis that synchronous pathogenicity and host development are necessary for incidence of sudden oak death disease was tested by correlating seasonal variations in host cambial phenology and response to inoculation with &lt;em&gt;Phytophthora ramorum.&lt;/em&gt;&lt;/p&gt;&lt;ul&gt;&lt;li&gt;&lt;span class=&quot;bullet&quot;&gt;• &lt;/span&gt;&lt;div class=&quot;text&quot;&gt;Response to infection was estimated by inoculating branch cuttings from coast live oak (&lt;em&gt;Quercus agrifolia&lt;/em&gt;) trees at nine dates through a full annual cycle in 2003–2004. Host phenology was estimated from measurements of bud burst and cambial activity in spring 2006.&lt;/div&gt;&lt;/li&gt;&lt;li&gt;&lt;span class=&quot;bullet&quot;&gt;• &lt;/span&gt;&lt;div class=&quot;text&quot;&gt;Lesions were largest in the spring soon after the cambium resumed activity. A moderate genetic component to lesion size was detected. Variation among trees in date of largest lesions correlated with variation in timing of bud burst and cambial phenology.&lt;/div&gt;&lt;/li&gt;&lt;li&gt;&lt;span class=&quot;bullet&quot;&gt;• &lt;/span&gt;&lt;div class=&quot;text&quot;&gt;The data support the hypothesis that active host cambial tissue is a necessary requisite for successful infection with the pathogen that causes sudden oak death canker disease. Genetic variation in host phenology will buffer coast live oak against epidemics of this disease.&lt;/div&gt;&lt;/li&gt;&lt;/ul&gt;</style></abstract></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Funahashi, F.</style></author><author><style face="normal" font="default" size="100%">Parke, J. L.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Effects of Soil Solarization and Trichoderma asperellum on Soilborne Inoculum of Phytophthora ramorum and Phytophthora pini in Container Nurseries</style></title><secondary-title><style face="normal" font="default" size="100%">Plant Disease</style></secondary-title><short-title><style face="normal" font="default" size="100%">Plant Disease</style></short-title></titles><dates><year><style  face="normal" font="default" size="100%">2016</style></year><pub-dates><date><style  face="normal" font="default" size="100%">Jan-02-2016</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://apsjournals.apsnet.org/doi/10.1094/PDIS-04-15-0453-RE</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">100</style></volume><pages><style face="normal" font="default" size="100%">438 - 443</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Infested container nursery beds are an important source of soilborne &lt;em&gt;Phytophthora&lt;/em&gt; spp. for initiating disease through movement with surface water or splashing onto foliage. We investigated the effects of soil solarization, alone or with subsequent amendment with a &lt;em&gt;Trichoderma asperellum&lt;/em&gt; biocontrol agent, on the survival of &lt;em&gt;Phytophthora&lt;/em&gt; spp. inoculum. In field trials conducted with &lt;em&gt;Phytophthora ramorum&lt;/em&gt; in San Rafael, CA and with &lt;em&gt;P. pini&lt;/em&gt; in Corvallis, OR, infested rhododendron leaf inoculum was buried at 5, 15, and 30 cm below the soil surface. Solarization for 2 or 4 weeks during summer 2012 eliminated recovery of &lt;em&gt;Phytophthora&lt;/em&gt; spp. buried at all depths in California trial 1, at 5 and 15 cm in California trial 2, but only at 5 cm in Oregon. There was no significant reduction of &lt;em&gt;Phytophthora&lt;/em&gt; spp. recovery after &lt;em&gt;T. asperellum&lt;/em&gt; application. Although the population densities of the introduced &lt;em&gt;T. asperellum&lt;/em&gt; at the 5-cm depth were often two- to fourfold higher in solarized compared with nonsolarized plots, they were not significantly different (&lt;em&gt;P&lt;/em&gt; = 0.052). Soil solarization appears to be a promising technique for disinfesting the upper layer of soil in container nurseries under certain conditions.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Gallego, F. J.</style></author><author><style face="normal" font="default" size="100%">Perez de Algaba, A.</style></author><author><style face="normal" font="default" size="100%">Fernandez-Escobar, R.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Etiology of oak decline in Spain</style></title><secondary-title><style face="normal" font="default" size="100%">European Journal of Forest Pathology</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">1999</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1046/j.1439-0329.1999.00128.x</style></url></web-urls></urls><number><style face="normal" font="default" size="100%">1</style></number><publisher><style face="normal" font="default" size="100%">Blackwell Publishing Ltd</style></publisher><volume><style face="normal" font="default" size="100%">29</style></volume><pages><style face="normal" font="default" size="100%">17–27</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;In different areas of Extremadura, Western Spain, soil samples were taken at the bottom of holm oak (&lt;em&gt;Quercus ilex&lt;/em&gt;) trees that were showing decline symptoms. Half of each sample was sterilized, and acorns were sown in both sterilized and nonsterilized soil samples. The resulting seedlings were used as baits for the isolation of fungi. Seedlings growing on the natural, nonsterilized substrate were characterized by having a lower vegetative growth than the ones growing on the sterilized soil samples, and most of them died. &lt;em&gt;Phytophthora cinnnamomi&lt;/em&gt; was consistently isolated from their roots. &lt;em&gt;Fusarium oxysporum&lt;/em&gt; was also isolated as well as different species of &lt;em&gt;Pythium&lt;/em&gt;, although to a lesser extent. Pathogenicity tests were performed on holm oak seedlings with five different isolates of &lt;em&gt;P. cinnamomi&lt;/em&gt;, with &lt;em&gt;F. oxysporum&lt;/em&gt;, &lt;em&gt;Pythium&lt;/em&gt; and with a mixture of the three fungi. All the inoculated seedlings with &lt;em&gt;P. cinnamomi&lt;/em&gt; developed root rot and grew slowly, and 35.7% of them died up to the end of the experiments. &lt;em&gt;P. cinnamomi&lt;/em&gt; was consistently isolated from their roots, indicating that this fungus is the causal agent of holm oak decline. However, &lt;em&gt;F. oxysporum&lt;/em&gt; caused similar symptoms on oak seedlings as &lt;em&gt;P. cinnamomi&lt;/em&gt;, and was isolated also from the roots, although its frequency was lower than that of &lt;em&gt;P. cinnamomi&lt;/em&gt;.&lt;/p&gt;</style></abstract></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Garbelotto, M.</style></author><author><style face="normal" font="default" size="100%">Harnik, T. Y.</style></author><author><style face="normal" font="default" size="100%">Schmidt, D. J.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Efficacy of phosphonic acid, metalaxyl-M and copper hydroxide against Phytophthora ramorum in vitro and in planta</style></title><secondary-title><style face="normal" font="default" size="100%">Plant Pathology</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">disease management</style></keyword><keyword><style  face="normal" font="default" size="100%">phenotypic variability</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus agrifolia</style></keyword><keyword><style  face="normal" font="default" size="100%">Sudden oak death</style></keyword><keyword><style  face="normal" font="default" size="100%">Umbellularia californica</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2009</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1111/j.1365-3059.2008.01894.x</style></url></web-urls></urls><number><style face="normal" font="default" size="100%">1</style></number><publisher><style face="normal" font="default" size="100%">Blackwell Publishing Ltd</style></publisher><volume><style face="normal" font="default" size="100%">58</style></volume><pages><style face="normal" font="default" size="100%">111–119</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;The ability of metalaxyl-M, phosphonic acid in the form of phosphonate, and copper hydroxide to inhibit different stages in the life cycle of &lt;em&gt;Phytophthora ramorum&lt;/em&gt;, the causal agent of sudden oak death (SOD), was tested in vitro using 12 isolates from the North American forest lineage. In addition, experiments were conducted in planta to study the ability of phosphonic acid injections and metalaxyl-M drenches to control pathogen growth on saplings of California coast live oak (&lt;em&gt;Quercus agrifolia&lt;/em&gt;), and of copper hydroxide foliar sprays to control infection of California bay laurel (&lt;em&gt;Umbellularia californica&lt;/em&gt;) leaves. &lt;em&gt;Phytophthora ramorum&lt;/em&gt; was only moderately sensitive to phosphonic acid in vitro, but was highly sensitive to copper hydroxide. In planta experiments indicated the broad efficacy of phosphonic acid injections and of copper hydroxide sprays in preventing growth of &lt;em&gt;P. ramorum&lt;/em&gt; in oaks and bay laurels, respectively. Finally, although metalaxyl-M was effective in vitro, drenches of potted oak trees using this active ingredient were largely ineffective in reducing the growth rate of the pathogen in planta.&lt;/p&gt;</style></abstract></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Grünwald, Niklaus J.</style></author><author><style face="normal" font="default" size="100%">Garbelotto, Matteo</style></author><author><style face="normal" font="default" size="100%">Goss, Erica M.</style></author><author><style face="normal" font="default" size="100%">Heungens, Kurt</style></author><author><style face="normal" font="default" size="100%">Prospero, Simone</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Emergence of the sudden oak death pathogen Phytophthora ramorum</style></title><secondary-title><style face="normal" font="default" size="100%">Trends in Microbiology</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2012</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://www.sciencedirect.com/science/article/pii/S0966842X11002277</style></url></web-urls></urls><number><style face="normal" font="default" size="100%">3</style></number><volume><style face="normal" font="default" size="100%">20</style></volume><pages><style face="normal" font="default" size="100%">131 - 138</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;The recently emerged plant pathogen &lt;em&gt;Phytophthora ramorum&lt;/em&gt; is responsible for causing the sudden oak death epidemic. This review documents the emergence of &lt;em&gt;P. ramorum&lt;/em&gt; based on evolutionary and population genetic analyses. Currently infection by &lt;em&gt;P. ramorum&lt;/em&gt; occurs only in Europe and North America and three clonal lineages are distinguished: EU1, NA1 and NA2. Ancient divergence of these lineages supports a scenario in which &lt;em&gt;P. ramorum&lt;/em&gt; originated from reproductively isolated populations and underwent at least four global migration events. This recent work sheds new light on mechanisms of emergence of exotic pathogens and provides crucial insights into migration pathways.&lt;/p&gt;</style></abstract></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Hansen, E.M.</style></author><author><style face="normal" font="default" size="100%">Kanaskie, A.</style></author><author><style face="normal" font="default" size="100%">Prospero, S</style></author><author><style face="normal" font="default" size="100%">McWilliams, M.</style></author><author><style face="normal" font="default" size="100%">Goheen, E. M.</style></author><author><style face="normal" font="default" size="100%">Osterbauer, N.</style></author><author><style face="normal" font="default" size="100%">P. Reeser</style></author><author><style face="normal" font="default" size="100%">Sutton, W.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Epidemiology of Phytophthora ramorum in Oregon tanoak forests</style></title><secondary-title><style face="normal" font="default" size="100%">Canadian Journal of Forest Research</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">Submitted</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://www.nrcresearchpress.com/doi/abs/10.1139/X07-217#.UNIUO7aKS0c</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">38</style></volume><pages><style face="normal" font="default" size="100%">1133-1143(11)</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;We followed the local intensification and dispersal of &lt;em&gt;Phytophthora ramorum&lt;/em&gt; Werres, De Cock, &amp;amp; Man In’t Veld in Oregon tanoak (&lt;em&gt;Lithocarpus densiflorus&lt;/em&gt; (Hook &amp;amp; Arn.) Rehd.) forests from its initial detection in 2001 through 2006, coincident with a continuing eradication effort. The initial infested area included nine scattered sites below 400m elevation, close to the Pacific Ocean near Brookings, Oregon. In subsequent years, one-half of new infections were within 122m of a previous infection, and 79% of the newly detected trees occurred within 300m of a previously identified tree. Dispersal up to 4km was occasionally recorded. Initial infection occurred in the upper crowns of tanoak trees. The pathogen was recovered in rainwater collected beneath diseased tanoak trees in every month from November 2006 through October 2007. Twenty-four multilocus microsatellite genotypes were identified among 272 &lt;em&gt;P. ramorum&lt;/em&gt; isolates collected from Curry County. Genotypic analysis provided independent estimates of time of origin of the Oregon infestation, its clustered distribution, and dispersal distances. In all sampling years, 60%-71% of the isolates belonged to the same multilocus genotype. In 2001, 12 genotypes were detected and new genotypes were identified in each of the subsequent years, but all isolates belonged to the same clonal lineage. Knowledge of local intensification of the disease and long-distance dispersal should inform both Oregon eradication efforts and national quarantine regulations.&lt;/p&gt;</style></abstract></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Holderness, M</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Efficacy of Neutralised Phosphonic Acid (Phosphorous Acid) Against Phytophthora Palmivora Pod Rot and Canker of Cocoa.</style></title><secondary-title><style face="normal" font="default" size="100%">Australasian Plant Pathology</style></secondary-title><short-title><style face="normal" font="default" size="100%">Austral. Plant Pathol.</style></short-title></titles><dates><year><style  face="normal" font="default" size="100%">1990</style></year><pub-dates><date><style  face="normal" font="default" size="100%">1990</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://link.springer.com/article/10.1071%2FAPP9900130</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">19</style></volume><pages><style face="normal" font="default" size="100%">130</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;In comparative trials under a wide range of environmental conditions and management inputs, injection of cocoa trees with partially pH-neutralised phosphonic acid (H&lt;sub class=&quot;a-plus-plus&quot;&gt;3&lt;/sub&gt;PO&lt;sub class=&quot;a-plus-plus&quot;&gt;3&lt;/sub&gt;) gave similar, or better, control of pod rot caused by &lt;em class=&quot;a-plus-plus&quot;&gt;Phytophthora palmivora&lt;/em&gt; to that obtained with metalaxyl/cuprous oxide pod sprays. lnjection reduced canker incidence by up to 90% at some sites. Foliar sprays of phosphonic acid had little effect on yield or pod rot incidence at rates up to 24 g a.i./tree/application. Studies to determine the optimum dose and frequency of injection have shown a clear benefit of treatment, with both increased yields and reduced pod rot incidence, but no yield advantage was obtained through high dose rates. Alginate gel paints and direct root uptake were evaluated as alternative application methods, but were less effective than injection. H&lt;sub class=&quot;a-plus-plus&quot;&gt;3&lt;/sub&gt;PO&lt;sub class=&quot;a-plus-plus&quot;&gt;3&lt;/sub&gt; was ineffective against vascular-streak dieback disease of cocoa, caused by &lt;em class=&quot;a-plus-plus&quot;&gt;Oncobasidium theobromae&lt;/em&gt;.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Jeffers, S. N.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Enhancing detection of Phytophthora cactorum in naturally infested soil</style></title><secondary-title><style face="normal" font="default" size="100%">Phytopathology</style></secondary-title><short-title><style face="normal" font="default" size="100%">Phytopathology</style></short-title></titles><dates><year><style  face="normal" font="default" size="100%">1987</style></year><pub-dates><date><style  face="normal" font="default" size="100%">1987</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">77</style></volume><pages><style face="normal" font="default" size="100%">1475</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Reliable methods were needed to detect &lt;em&gt;P. cactorum, &lt;/em&gt;one of the primary causal agents of &lt;em&gt;P. &lt;/em&gt;crown rot of apple trees, in its natural soil environment. Apple or pear fruits, used in a baiting bioassay, were ineffective at detecting &lt;em&gt;P. cactorum &lt;/em&gt;in naturally infested soil. Apple seedlings, cotyledons and seedling leaf pieces were successful baits, but cotyledons were the most sensitive and efficient. Completely air drying soil subsamples and then remoistening them for several days before flooding and adding plant tissue baits (extended baiting procedure) greatly enhanced detection when compared with the standard direct baiting procedure without prior manipulation of soil moisture. Bioassay incubation temp., volume of water added to remoisten air-dried soil subsamples, and incubation period following remoistening all affected detection, but the photoperiod during incubation did not. The advantages of an extended baiting bioassay with apple cotyledons were: greater sensitivity than with pear or apple fruits or by direct baiting, readily available and inexpensive baits, formation of sporangia of &lt;em&gt;P. cactorum &lt;/em&gt;directly on necrotic cotyledons, and lack of interference by contaminating &lt;em&gt;Pythium &lt;/em&gt;species. Cotyledons were also colonized by zoospores of &lt;em&gt;P. cambivora, P. citricola &lt;/em&gt;and &lt;em&gt;P. cryptogea, &lt;/em&gt;but not by those of &lt;em&gt;P. megasperma, P. syringae, P. drechsleri, &lt;/em&gt;or an unidentified &lt;em&gt;Phytophthora &lt;/em&gt;sp. The extended bioassay procedure routinely has provided a relatively rapid and efficient means of detecting &lt;em&gt;P. cactorum &lt;/em&gt;in a diversity of soils within and around New York apple orchards.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">10</style></issue></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Kong, P.</style></author><author><style face="normal" font="default" size="100%">Lea-Cox, J. D.</style></author><author><style face="normal" font="default" size="100%">Hong, C. X.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Effect of electrical conductivity on survival of Phytophthora alni, P. kernoviae and P. ramorum in a simulated aquatic environment</style></title><secondary-title><style face="normal" font="default" size="100%">Plant Pathology</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">aquatic biology</style></keyword><keyword><style  face="normal" font="default" size="100%">electrical conductivity</style></keyword><keyword><style  face="normal" font="default" size="100%">quarantine pathogen</style></keyword><keyword><style  face="normal" font="default" size="100%">zoospores</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2012</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1111/j.1365-3059.2012.02614.x</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">Blackwell Publishing Ltd</style></publisher><volume><style face="normal" font="default" size="100%">61</style></volume><pages><style face="normal" font="default" size="100%">1179–1186</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;This study investigated survival of the pathogens &lt;em&gt;Phytophthora ramorum&lt;/em&gt;, &lt;em&gt;P.&amp;nbsp;alni&lt;/em&gt; and &lt;em&gt;P.&amp;nbsp;kernoviae&lt;/em&gt; as zoospores or sporangia in response to an important water quality parameter, electrical conductivity (EC), at its range in irrigation water reservoirs and irrigated cropping systems. Experiments with different strengths of Hoagland’s solution showed that all three pathogens survived at a broad range of EC levels for at least 3&amp;nbsp;days and were stimulated to grow and sporulate at ECs&amp;nbsp;&amp;gt;&amp;nbsp;1·89&amp;nbsp;dS&amp;nbsp;m&lt;sup&gt;-1&lt;/sup&gt;. Recovery of initial populations after a 14-day exposure was over 20% for &lt;em&gt;P.&amp;nbsp;alni&lt;/em&gt; subsp. &lt;em&gt;alni&lt;/em&gt; and &lt;em&gt;P.&amp;nbsp;kernoviae&lt;/em&gt;, and 61·3% and 130% for zoospores and sporangia of &lt;em&gt;P.&amp;nbsp;ramorum&lt;/em&gt;, respectively. Zoospore survival of these pathogens at ECs&amp;nbsp;&amp;lt;&amp;nbsp;0·41&amp;nbsp;dS&amp;nbsp;m&lt;sup&gt;-1&lt;/sup&gt; was poor, barely beyond 3&amp;nbsp;days in pure water; only 0·3% (&lt;em&gt;P.&amp;nbsp;alni&lt;/em&gt;), 2·9% (&lt;em&gt;P.&amp;nbsp;kernoviae&lt;/em&gt;) and 15·1% (&lt;em&gt;P.&amp;nbsp;ramorum&lt;/em&gt;) of the initial population survived after 14&amp;nbsp;days at EC&amp;nbsp;=&amp;nbsp;0·21&amp;nbsp;dS&amp;nbsp;m&lt;sup&gt;-1&lt;/sup&gt;. The variation in rates of survival at different EC levels suggests that these pathogens survive better in cropping systems than in irrigation water. Containment of run-off and reduction in EC levels may therefore be non-chemical control options to reduce the risk of pathogen spread through natural waterways and irrigation systems.&lt;/p&gt;</style></abstract></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Loo, Judy</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Ecological impacts of non-indigenous invasive fungi as forest pathogens</style></title><secondary-title><style face="normal" font="default" size="100%">Biological Invasions</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2009</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1007/s10530-008-9321-3</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">Springer Netherlands</style></publisher><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">81-96</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><notes><style face="normal" font="default" size="100%">10.1007/s10530-008-9321-3</style></notes></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Meadows, I. M.</style></author><author><style face="normal" font="default" size="100%">Zwart, D. C.</style></author><author><style face="normal" font="default" size="100%">Jeffers, S. N.</style></author><author><style face="normal" font="default" size="100%">Waldrop, T. A.</style></author><author><style face="normal" font="default" size="100%">Bridges, W. C.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Effects of fuel reduction treatments on incidence of Phytophthora species in soil of a southern Appalachian Mountain forest</style></title><secondary-title><style face="normal" font="default" size="100%">Plant Disease</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2011</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://apsjournals.apsnet.org/doi/abs/10.1094/PDIS-07-10-0505</style></url></web-urls></urls><number><style face="normal" font="default" size="100%">7</style></number><volume><style face="normal" font="default" size="100%">95</style></volume><pages><style face="normal" font="default" size="100%">811-820</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;The National Fire and Fire Surrogate Study was initiated to study the effects of fuel reduction treatments on forest ecosystems. Four fuel reduction treatments were applied to three sites in a southern Appalachian Mountain forest in western North Carolina: prescribed burning, mechanical fuel reduction, mechanical fuel reduction followed by prescribed burning, and a nontreated control. To determine the effects of fuel reduction treatments on &lt;em&gt;Phytophthora&lt;/em&gt; spp. in soil, incidences were assessed once before and twice after fuel reduction treatments were applied. Also, the efficiency of the baiting bioassay used to detect species of &lt;em&gt;Phytophthora&lt;/em&gt; was evaluated, and the potential virulence of isolates of &lt;em&gt;Phytophthora&lt;/em&gt; spp. collected from forest soils was determined. &lt;em&gt;Phytophthora cinnamomi&lt;/em&gt; and &lt;em&gt;P. heveae&lt;/em&gt; were the only two species recovered from the study site. Incidences of these species were not significantly affected by fuel reduction treatments, but incidence of &lt;em&gt;P. cinnamomi&lt;/em&gt; increased over time. In the baiting bioassay, camellia leaf disks were better than hemlock needles as baits. &lt;em&gt;P. cinnamomi&lt;/em&gt; was detected best in fresh soil, whereas &lt;em&gt;P. heveae&lt;/em&gt; was detected best when soil was air-dried and remoistened prior to baiting. Isolates of &lt;em&gt;P. heveae&lt;/em&gt; were weakly virulent and, therefore, potentially pathogenic—causing lesions only on wounded mountain laurel and rhododendron leaves; however, isolates of &lt;em&gt;P. cinnamomi&lt;/em&gt; were virulent and caused root rot and mortality on mountain laurel and white pine plants.&lt;/p&gt;</style></abstract></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Meentemeyer, Ross K.</style></author><author><style face="normal" font="default" size="100%">Cunniffe, Nik J.</style></author><author><style face="normal" font="default" size="100%">Cook, Alex R.</style></author><author><style face="normal" font="default" size="100%">Filipe, Joao A. N.</style></author><author><style face="normal" font="default" size="100%">Hunter, Richard D.</style></author><author><style face="normal" font="default" size="100%">Rizzo, David M.</style></author><author><style face="normal" font="default" size="100%">Gilligan, Christopher A.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Epidemiological modeling of invasion in heterogeneous landscapes: spread of sudden oak death in California (1990–2030)</style></title><secondary-title><style face="normal" font="default" size="100%">Ecosphere</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2011</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://www.esajournals.org/doi/abs/10.1890/ES10-00192.1</style></url></web-urls></urls><number><style face="normal" font="default" size="100%">2</style></number><volume><style face="normal" font="default" size="100%">2</style></volume><pages><style face="normal" font="default" size="100%">art17</style></pages><language><style face="normal" font="default" size="100%">eng</style></language></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Morales-Rodríguez, C.</style></author><author><style face="normal" font="default" size="100%">Vettraino, A. M.</style></author><author><style face="normal" font="default" size="100%">Vannini, Á.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Efficacy of Biofumigation with Brassica carinata Commercial Pellets (BioFence) to Control Vegetative and Reproductive Structures of Phytophthora cinnamomi</style></title><secondary-title><style face="normal" font="default" size="100%">Plant Disease</style></secondary-title><short-title><style face="normal" font="default" size="100%">Plant Disease</style></short-title></titles><dates><year><style  face="normal" font="default" size="100%">2016</style></year><pub-dates><date><style  face="normal" font="default" size="100%">Jan-02-2016</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://apsjournals.apsnet.org/doi/10.1094/PDIS-03-15-0245-RE</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">100</style></volume><pages><style face="normal" font="default" size="100%">324 - 330</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;The efficacy of biofumigation with &lt;em&gt;Brassica carinata&lt;/em&gt; pellets (BioFence) to control vegetative and reproductive structures of &lt;em&gt;Phytophthora cinnamomi&lt;/em&gt; was investigated in vitro at different doses and temperatures. Biofumigation was effective in inhibiting mycelial growth (culture diameter) and chlamydospore and zoospore germination, and was lethal at 24 mg of pellet per plate (approximately 0.4 mg/liter). The 50% effective concentration values showed that efficacy of &lt;em&gt;B. carinata&lt;/em&gt; pellets in inhibiting or killing the vegetative and reproductive structures of &lt;em&gt;P. cinnamomi&lt;/em&gt; was maximum at 15°C and decreased as temperature rose to 25°C. However, the fungicide effect was independent of the temperature. In vivo biofumigation of &lt;em&gt;Quercus cerris&lt;/em&gt; seedlings with BioFence confirmed efficacy by reducing the inoculum density (CFU/g) of &lt;em&gt;P. cinnamomi&lt;/em&gt;, thus protecting the host from root infection. The use of BioFence provides an alternative to synthetic pesticides to control &lt;em&gt;P. cinnamomi&lt;/em&gt; within disease management programs in agroforestry systems.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Moricca, Salvatore</style></author><author><style face="normal" font="default" size="100%">Linaldeddu, Benedetto T.</style></author><author><style face="normal" font="default" size="100%">Ginetti, Beatrice</style></author><author><style face="normal" font="default" size="100%">Scanu, Bruno</style></author><author><style face="normal" font="default" size="100%">Franceschini, Antonio</style></author><author><style face="normal" font="default" size="100%">Ragazzi, Alessandro</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Endemic and Emerging Pathogens Threatening Cork Oak Trees: Management Options for Conserving a Unique Forest Ecosystem</style></title><secondary-title><style face="normal" font="default" size="100%">Plant Disease</style></secondary-title><short-title><style face="normal" font="default" size="100%">Plant Disease</style></short-title></titles><dates><year><style  face="normal" font="default" size="100%">2016</style></year><pub-dates><date><style  face="normal" font="default" size="100%">Jan-11-2016</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://apsjournals.apsnet.org/doi/10.1094/PDIS-03-16-0408-FE</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">100</style></volume><pages><style face="normal" font="default" size="100%">2184 - 2193</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Cork oak (&lt;em&gt;Quercus suber&lt;/em&gt;) forests are economically and culturally intertwined with the inhabitants of the Mediterranean basin and characterize its rural landscape. These forests cover over two million hectares in the western Mediterranean basin and sustain a rich biodiversity of endemisms as well as representing an important source of income derived from cork production. Currently cork oak forests are threatened by several factors including human-mediated disturbances such as poor or inappropriate management practices, adverse environmental conditions (irregular water regime with prolonged drought periods), and attacks of pathogens and pests. All these adverse factors can interact, causing a complex disease commonly known as “oak decline.” Despite the numerous investigations carried out so far, decline continues to be the main pathological problem of cork oak forests because of its complex etiology and the resulting difficulties in defining suitable control strategies. An overview of the literature indicates that several pathogenic fungi and oomycota can play a primary role in the etiology of this syndrome. Therefore, the aim of this review is to analyze the recent advances achieved regarding the bio-ecology of the endemic and emerging pathogens that threaten cork oak trees with particular emphasis on the species more directly involved in oak decline. Moreover, the effect of climate change on the host-pathogen interactions, a task fundamental for making useful decisions and managing cork oak forests properly, is considered.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">11</style></issue></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Pohe, J.</style></author><author><style face="normal" font="default" size="100%">Dongo, BK</style></author><author><style face="normal" font="default" size="100%">N’Goran, N.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Effectiveness of aluminum-fosetyl in the control of early nutfall of coconut tree due to Phytophthora katsurae (Pythiaceae)</style></title><secondary-title><style face="normal" font="default" size="100%">Agronomie africaine</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2009</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://www.ajol.info/index.php/aga/article/view/1633</style></url></web-urls></urls><number><style face="normal" font="default" size="100%">3</style></number><volume><style face="normal" font="default" size="100%">15</style></volume><pages><style face="normal" font="default" size="100%">123–133</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Early nut fall and bud rot due to &lt;em&gt;Phytophthora katsurae&lt;/em&gt; are the most important diseases of coconut tree observed in recent years at the Assinie plantations of PALMINDUSTRIE Company, Côte d’Ivoire. Field investigations conducted in 1983 revealed a high rate of nut fall (50-70%) during the rainy season. Cutting of coconut stands with rotten buds, as a way to control the spread of &lt;em&gt;Oryctes&lt;/em&gt; sp., allowed to assess the number of dead trees over 139 and 89 ha of land for the hybrids and Grand West cultivars, respectively. In addition to those disease control measures proposed by the Company, comparison trials were systematically carried out using 2 fungicides: aluminum-fosetyl [fosetyl] at 3 doses (3.2, 4.8 and 6.4 g of active ingredient/tree) and Ridomil [metalaxyl] at one dose (3.125 g of active ingredient/tree). These fungicide were injected into the stem of the coconut every 3 months starting from December 1984. After 3 years, the efficacy of the 3 doses of aluminium-fosetyl over Ridomil in significantly reducing nut fall, even at low rates (3.2 g of active ingredient/tree), was apparent. However, the technique still remains out of reach of most farmers because of lack of technical know-how. It appears therefore, that an improvement of the technique, so as to make it accessible to the farmers, is a necessity.&lt;/p&gt;</style></abstract></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ríos, Pedro</style></author><author><style face="normal" font="default" size="100%">Obergón, Sara</style></author><author><style face="normal" font="default" size="100%">de Haro, Antonio</style></author><author><style face="normal" font="default" size="100%">Fernández-Rebollo, Pilar</style></author><author><style face="normal" font="default" size="100%">Serrano, María-Socorro</style></author><author><style face="normal" font="default" size="100%">Sánchez, María-Esperanza</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Effect of Brassica Biofumigant Amendments on Different Stages of the Life Cycle of Phytophthora cinnamomi</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Phytopathology</style></secondary-title><short-title><style face="normal" font="default" size="100%">J Phytopathol</style></short-title></titles><dates><year><style  face="normal" font="default" size="100%">2016</style></year><pub-dates><date><style  face="normal" font="default" size="100%">Jan-05-2016</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://doi.wiley.com/10.1111/jph.12482http://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fjph.12482</style></url></web-urls></urls><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;The oomycete plant pathogen &lt;em&gt;Phytophthora cinnamomi&lt;/em&gt; causes a highly destructive root rot that affects numerous hosts. Integrated management strategies are needed to control &lt;em&gt;P.&amp;nbsp;cinnamomi&lt;/em&gt; in seminatural oak rangelands. We tested how biofumigation affects crucial stages of the pathogen's life cycle &lt;em&gt;in&amp;nbsp;vitro&lt;/em&gt;, in infested soils under laboratory conditions and &lt;em&gt;in planta&lt;/em&gt;. Different genotypes of three potential biofumigant plant species (&lt;em&gt;Brassica carinata, Brassica juncea, Brassica napus&lt;/em&gt;) were collected at different phenological stages, analysed for their glucosinolate contents, and subsequently tested. The most effective genotypes against mycelial growth and sporangial production were further tested on the viability of chlamydospores in artificially infested natural soils and &lt;em&gt;in planta&lt;/em&gt; on &lt;em&gt;Lupinus luteus&lt;/em&gt;, a host highly susceptible to &lt;em&gt;P.cinnamomi&lt;/em&gt;. &lt;em&gt;Brassica carinata&lt;/em&gt; and &lt;em&gt;B.&amp;nbsp;juncea&lt;/em&gt; genotypes inhibited mycelial growth, decreased sporangial production, and effectively inhibited the viability of chlamydospores in soil, but only &lt;em&gt;B.&amp;nbsp;carinata&lt;/em&gt; decreased disease symptoms in plants. Effective genotypes of &lt;em&gt;Brassica&lt;/em&gt; had high levels of the glucosinolate sinigrin. Biofumigation with Brassica plants rich in sinigrin has potential to be a suitable tool for control of oak root disease caused by &lt;em&gt;P.&amp;nbsp;cinnamomi&lt;/em&gt; in Spanish oak rangeland ecosystems.&lt;/p&gt;</style></abstract></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Shelley, B. A.</style></author><author><style face="normal" font="default" size="100%">Luster, D. G.</style></author><author><style face="normal" font="default" size="100%">Garrett, W. M.</style></author><author><style face="normal" font="default" size="100%">McMahon, M. B.</style></author><author><style face="normal" font="default" size="100%">Widmer, T. L.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Effects of temperature on germination of sporangia, infection and protein secretion by Phytophthora kernoviae</style></title><secondary-title><style face="normal" font="default" size="100%">Plant Pathology</style></secondary-title><short-title><style face="normal" font="default" size="100%">Plant Pathol</style></short-title></titles><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">Jan-04-2018</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1111/ppa.12782</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">67</style></volume><pages><style face="normal" font="default" size="100%">719 - 728</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;&lt;em&gt;Phytophthora kernoviae&lt;/em&gt; is a pathogen on a wide range of plants, but little is known of optimal infection conditions. &lt;em&gt;Rhododendron ponticum&lt;/em&gt; leaves were inoculated with six different isolates of &lt;em&gt;P.&amp;nbsp;kernoviae&lt;/em&gt; sporangia and incubated at different temperatures from 10 to 28&amp;nbsp;°C. After 1&amp;nbsp;week, lesion development and pathogen recovery were only observed from all isolates at 15 and 20&amp;nbsp;°C and a few isolates at 10&amp;nbsp;°C. In an experiment with temperatures ranging from 20 to 25&amp;nbsp;°C, lesion development and pathogen recovery on &lt;em&gt;R.&amp;nbsp;ponticum&lt;/em&gt;,&lt;em&gt; Magnolia stellata&lt;/em&gt; and &lt;em&gt;Viburnum tinus&lt;/em&gt; occurred consistently at 20 and 21&amp;nbsp;°C, was limited at 22&amp;nbsp;°C, and did not occur at 23&amp;nbsp;°C and above. There was no difference in sporangia and zoospore germination at 20–25&amp;nbsp;°C. In a temperature fluctuation experiment, the necrotic area of inoculated &lt;em&gt;R.&amp;nbsp;ponticum&lt;/em&gt; leaves increased with longer incubation at 20&amp;nbsp;°C and decreased with longer incubation at 24&amp;nbsp;°C. Crude extracts of secreted proteins from &lt;em&gt;P.&amp;nbsp;kernoviae&lt;/em&gt; cultures grown at 20 and 24&amp;nbsp;°C were compared to determine any effects of temperature on pathogenicity. When spot tested on &lt;em&gt;R.&amp;nbsp;ponticum&lt;/em&gt; leaves, crude protein suspensions from cultures grown at 20&amp;nbsp;°C induced necrosis, while proteins from cultures grown at 24&amp;nbsp;°C did not. Proteomic analysis confirmed that a 10&amp;nbsp;kDa protein secreted at both 20 and 24&amp;nbsp;°C shared sequence homology to the conserved domains of known elicitins of other &lt;em&gt;Phytophthora&lt;/em&gt; spp. The protein secreted at 20&amp;nbsp;°C that was responsible for necrosis has not been identified.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Tooley, Paul W.</style></author><author><style face="normal" font="default" size="100%">Browning, Marsha</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">The Effect of Exposure to Decreasing Relative Humidity on the Viability of Phytophthora ramorum sporangia</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Phytopathology</style></secondary-title><short-title><style face="normal" font="default" size="100%">J Phytopathol</style></short-title></titles><dates><year><style  face="normal" font="default" size="100%">2016</style></year><pub-dates><date><style  face="normal" font="default" size="100%">Aug 2016</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1111/jph.12506 </style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">164</style></volume><pages><style face="normal" font="default" size="100%">874 - 881</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Sporangia of three isolates of &lt;em&gt;Phytophthora ramorum&lt;/em&gt; representing three different clonal lineages were subjected to relative humidity (RH) levels between 80 and 100% for exposure periods ranging from 1 to 24&amp;nbsp;h at 20°C in darkness. Plastic containers (21.5&amp;nbsp;×&amp;nbsp;14.5&amp;nbsp;×&amp;nbsp;5&amp;nbsp;cm) were used as humidity chambers with 130&amp;nbsp;ml of glycerine solution added to each container. Glycerine concentrations corresponded to 100, 95, 90, 85 and 80% RH based on refractive index measurements. Sporangia suspensions were pipeted onto nitrile mesh squares (1.5&amp;nbsp;×&amp;nbsp;1.5&amp;nbsp;cm, 15 micron pore size) which were placed in the humidity chambers and incubated at 20°C in darkness. Following exposure periods of 1, 2, 4, 8, 12 and 24&amp;nbsp;h, mesh squares were inverted onto Petri dishes of selective medium and sporangia germination assessed after 24 and 48&amp;nbsp;h. At 100% RH, we observed a mean value of 88% germination after 1&amp;nbsp;h exposure declining to 18% germination following 24&amp;nbsp;h incubation. At 95% RH, a steeper decline in germination was noted, with means ranging from 79% at 1&amp;nbsp;h to less than 1% at 24&amp;nbsp;h exposure. At 90% RH, no germination was noted after 8 or more h exposure, and values were 57%, 22% and 3% germination for the 1, 2 and 4&amp;nbsp;h exposures, respectively. Germination was only observed at 1&amp;nbsp;h exposure for both the 85% RH treatment (52% germination) and the 80% RH treatment (38% germination). The three isolates responded similarly&amp;nbsp;over the range of RH values tested. The germination response of &lt;em&gt;P.&amp;nbsp;ramorum&lt;/em&gt; sporangia to RH values between 80% and 100% was comparable to that reported for other &lt;em&gt;Phytophthora&lt;/em&gt; species. Knowledge of conditions that affect &lt;em&gt;P&lt;/em&gt;.&amp;nbsp;&lt;em&gt;ramorum&lt;/em&gt; sporangia germination can shed light on pathogenesis and epidemic potential and lead to improved control recommendations.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">11-12</style></issue></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Tooley, Paul W.</style></author><author><style face="normal" font="default" size="100%">Browning, Marsha</style></author><author><style face="normal" font="default" size="100%">Leighty, Robert M.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Effects of Inoculum Density and Wounding on Stem Infection of Three Eastern US Forest Species by Phytophthora ramorum</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Phytopathology</style></secondary-title><short-title><style face="normal" font="default" size="100%">J Phytopathol</style></short-title></titles><dates><year><style  face="normal" font="default" size="100%">2014</style></year><pub-dates><date><style  face="normal" font="default" size="100%">Jan-03-2014</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://doi.wiley.com/10.1111/jph.12251</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">162</style></volume><pages><style face="normal" font="default" size="100%">683 - 689</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Seedlings of three Eastern US forest species &lt;em&gt;Quercus rubra&lt;/em&gt; (northern red oak), &lt;em&gt;Quercus prinus&lt;/em&gt; (chestnut oak) and &lt;em&gt;Acer rubrum&lt;/em&gt; (red maple) were inoculated by applying &lt;em&gt;Phytophthora ramorum&lt;/em&gt; sporangia to stems at different inoculum densities with and without wounding. Disease occurred in all treatments involving wounds, and no disease was observed in unwounded treatments. Younger seedlings (2–3&amp;nbsp;years old) did not differ significantly from older seedlings (5–6&amp;nbsp;years old) in disease incidence, but older seedlings sustained smaller lesions compared with younger seedlings. For both old and young seedlings, disease on wounded stems was observed down to the lowest sporangia concentration utilized (500 sporangia/ml for old seedlings and 100 sporangia/ml for young seedlings). The results show that in the presence of wounding, even very low sporangia concentrations can result in disease, and further suggest that wounding caused by insects and other factors may play an important role in &lt;em&gt;P.&amp;nbsp;ramorum&lt;/em&gt; epidemiology in forest environments.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">10</style></issue></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Tooley, Paul W.</style></author><author><style face="normal" font="default" size="100%">Carras, Marie M.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Enhanced recovery of Phytophthora ramorum from soil following 30 Days of storage at 4°C</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Phytopathology</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">chlamydospore</style></keyword><keyword><style  face="normal" font="default" size="100%">ramorum blight</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2011</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1111/j.1439-0434.2011.01810.x</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">Blackwell Publishing Ltd</style></publisher><pages><style face="normal" font="default" size="100%">no–no</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Chlamydospores of &lt;em&gt;Phytophthora ramorum&lt;/em&gt; were used to infest field soil at densities ranging from 0.2 to 42 chlamydospores/cm3 soil. Recovery was determined by baiting with rhododendron leaf discs and dilution plating at time 0 and after 30&amp;nbsp;days of storage at 4°C, as recommended by USDA-APHIS. Baiting was slightly more sensitive than dilution plating in recovering &lt;em&gt;P.&amp;nbsp;ramorum&lt;/em&gt; immediately following infestation of soil and allowed detection from samples infested with as little as 0.2&amp;nbsp;chlamydospores/cm3 compared with 1 chlamydospore/cm3 for dilution plating. After 30&amp;nbsp;days of infested soil storage at 4°C, &lt;em&gt;P.&amp;nbsp;ramorum&lt;/em&gt; was detected at significantly (P&amp;nbsp;=&amp;nbsp;0.05) higher levels than at time 0 with both recovery methods. The results indicate that storage of &lt;em&gt;P.&amp;nbsp;ramorum&lt;/em&gt;-infested soil at 4°C may allow for pathogen activity, such as sporangia production, which may enhance recovery from soil.&lt;/p&gt;</style></abstract></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>32</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Torgeson,DC</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Epiphytology and etiology of a Phytophthora-induced root rot diseases of Chamaecyparis in Oregon</style></title></titles><dates><year><style  face="normal" font="default" size="100%">1953</style></year></dates><publisher><style face="normal" font="default" size="100%">Oregon State College</style></publisher><pub-location><style face="normal" font="default" size="100%">Corvallis, OR</style></pub-location><volume><style face="normal" font="default" size="100%">PhD</style></volume><pages><style face="normal" font="default" size="100%">72</style></pages><language><style face="normal" font="default" size="100%">eng</style></language></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">A.M. Vettraino</style></author><author><style face="normal" font="default" size="100%">Belisario, A.</style></author><author><style face="normal" font="default" size="100%">Maccaroni, M.</style></author><author><style face="normal" font="default" size="100%">A. Vannini</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Evaluation of root damage to English walnut caused by five Phytophthora species</style></title><secondary-title><style face="normal" font="default" size="100%">Plant Pathology</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">English walnut</style></keyword><keyword><style  face="normal" font="default" size="100%">Juglans regia</style></keyword><keyword><style  face="normal" font="default" size="100%">pathogenicity</style></keyword><keyword><style  face="normal" font="default" size="100%">soilborne pathogens</style></keyword><keyword><style  face="normal" font="default" size="100%">walnut decline</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2003</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1046/j.1365-3059.2003.00864.x</style></url></web-urls></urls><number><style face="normal" font="default" size="100%">4</style></number><publisher><style face="normal" font="default" size="100%">Blackwell Science Ltd</style></publisher><volume><style face="normal" font="default" size="100%">52</style></volume><pages><style face="normal" font="default" size="100%">491–495</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;The pathogenicity of five species of &lt;em&gt;Phytophthora&lt;/em&gt; to English walnut was studied in a greenhouse experiment. &lt;em&gt;Phytophthora cinnamomi&lt;/em&gt; was the most aggressive species, causing severe root rot and seedling mortality. The other species tested, &lt;em&gt;P. cambivora&lt;/em&gt;, &lt;em&gt;P. citricola&lt;/em&gt;, &lt;em&gt;P. cactorum&lt;/em&gt; and &lt;em&gt;P. cryptogea&lt;/em&gt;, did not induce visible crown symptoms on seedlings 2 months after inoculation. Some strains of &lt;em&gt;P. cambivora&lt;/em&gt; and &lt;em&gt;P. cactorum&lt;/em&gt; also caused taproot damage to seedlings. All except one of the tested isolates caused significant necrosis of fine roots and a significant reduction of root weight compared with noninoculated seedlings. Reduction of above-ground plant development was not statistically significant. While &lt;em&gt;P. cinnamomi&lt;/em&gt; is well known as an aggressive primary pathogen of English walnut, the other species of &lt;em&gt;Phytophthora&lt;/em&gt; may act as predisposing factors to walnut decline, affecting root system development and increasing host vulnerability to environmental stress.&lt;/p&gt;</style></abstract></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Zobel, D.B.</style></author><author><style face="normal" font="default" size="100%">L.F. Roth</style></author><author><style face="normal" font="default" size="100%">G.M. Hawk</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Ecology, pathology and management of Port-orford Cedar (Chamaecyparis lawsoniana).</style></title></titles><dates><year><style  face="normal" font="default" size="100%">1985</style></year></dates><publisher><style face="normal" font="default" size="100%">USDA Forest Service, Pacific Northwest Forest and Range Experiment Station, Portland, OR.</style></publisher><pages><style face="normal" font="default" size="100%">161 pp.</style></pages><language><style face="normal" font="default" size="100%">eng</style></language></record></records></xml>