<?xml version="1.0" encoding="UTF-8"?><xml><records><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%">Aguayo, Jaime</style></author><author><style face="normal" font="default" size="100%">Adams, Gerard C.</style></author><author><style face="normal" font="default" size="100%">Halkett, Fabien</style></author><author><style face="normal" font="default" size="100%">Catal, Mursel</style></author><author><style face="normal" font="default" size="100%">Husson, Claude</style></author><author><style face="normal" font="default" size="100%">Nagy, Zoltán A.</style></author><author><style face="normal" font="default" size="100%">Hansen, Everett M.</style></author><author><style face="normal" font="default" size="100%">Benoît Marçais</style></author><author><style face="normal" font="default" size="100%">Pascal Frey</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Strong genetic differentiation between North American and European populations of Phytophthora alni subsp. uniformis</style></title><secondary-title><style face="normal" font="default" size="100%">Phytopathology</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://dx.doi.org/10.1094/PHYTO-05-12-0116-R</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;Alder decline caused by &lt;em&gt;Phytophthora alni&lt;/em&gt; has been one of the most important diseases of natural ecosystems in Europe during the last 20 years. The emergence of &lt;em&gt;Phytophthora alni&lt;/em&gt; subsp. &lt;em&gt;alni&lt;/em&gt; (Paa)—the pathogen responsible for the epidemic—is linked to an interspecific hybridization event between two parental species: &lt;em&gt;Phytophthora alni&lt;/em&gt; subsp. &lt;em&gt;multiformis&lt;/em&gt; (Pam) and &lt;em&gt;Phytophthora alni&lt;/em&gt; subsp. &lt;em&gt;uniformis&lt;/em&gt; (Pau). One of the parental species, Pau, has been isolated in several European countries and recently in North America. The objective of this work was to assess the level of genetic diversity, the population genetic structure, and the putative reproduction mode and mating system of Pau. Five new polymorphic microsatellite markers were used to contrast both geographical populations. The study comprised 71 isolates of Pau collected from 8 European countries and 10 locations in North America. Our results revealed strong differences between continental populations (Fst=0.88; Rst=0.74), with no evidence for gene flow. European isolates showed extremely low genetic diversity compared to the North American collection. Selfing appears to be the predominant mating system in both continental collections. The results suggest that the European Pau population is most likely alien and derives from the introduction of a few individuals, while the North American population probably is an indigenous population.&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%">Amoroso, Mariano M.</style></author><author><style face="normal" font="default" size="100%">Larson, Bruce C.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Stand development patterns as a consequence of the mortality in Austrocedrus chilensis forests</style></title><secondary-title><style face="normal" font="default" size="100%">Forest Ecology and Management</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Austrocedrus chilensis</style></keyword><keyword><style  face="normal" font="default" size="100%">mortality</style></keyword><keyword><style  face="normal" font="default" size="100%">Stand dynamics</style></keyword><keyword><style  face="normal" font="default" size="100%">Uneven-aged</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2010</style></year><pub-dates><date><style  face="normal" font="default" size="100%">APR 30</style></date></pub-dates></dates><number><style face="normal" font="default" size="100%">{10}</style></number><publisher><style face="normal" font="default" size="100%">{ELSEVIER SCIENCE BV}</style></publisher><pub-location><style face="normal" font="default" size="100%">{PO BOX 211, 1000 AE AMSTERDAM, NETHERLANDS}</style></pub-location><volume><style face="normal" font="default" size="100%">259</style></volume><pages><style face="normal" font="default" size="100%">1981-1992</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%">Ashby, S.F.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Strains and taxonomy of Phytophthora palmivora Butler (P. Faberi Maubl.)</style></title><secondary-title><style face="normal" font="default" size="100%">Transactions of the British Mycological Society</style></secondary-title><short-title><style face="normal" font="default" size="100%">Transactions of the British Mycological Society</style></short-title></titles><dates><year><style  face="normal" font="default" size="100%">1929</style></year><pub-dates><date><style  face="normal" font="default" size="100%">Jan-03-1929</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://linkinghub.elsevier.com/retrieve/pii/S0007153629800253</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">14</style></volume><pages><style face="normal" font="default" size="100%">18 - 38</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><issue><style face="normal" font="default" size="100%">1-2</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%">Brasier,Clive</style></author><author><style face="normal" font="default" size="100%">Denman,Sandra</style></author><author><style face="normal" font="default" size="100%">Brown,Anna</style></author><author><style face="normal" font="default" size="100%">Webber,Joan</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Sudden oak death (Phytophthora ramorum) discovered on trees in Europe</style></title><secondary-title><style face="normal" font="default" size="100%">Mycological Research</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2004</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1017/S0953756204221244</style></url></web-urls></urls><number><style face="normal" font="default" size="100%">10</style></number><volume><style face="normal" font="default" size="100%">108</style></volume><pages><style face="normal" font="default" size="100%">1108-1110</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%">Brasier,Clive</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Sudden Oak Death: Phytophthora ramorum exhibits transatlantic differences</style></title><secondary-title><style face="normal" font="default" size="100%">Mycological Research</style></secondary-title></titles><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/10.1017/S0953756203227660</style></url></web-urls></urls><number><style face="normal" font="default" size="100%">03</style></number><volume><style face="normal" font="default" size="100%">107</style></volume><pages><style face="normal" font="default" size="100%">257-259</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%">Chastagner, G.A.</style></author><author><style face="normal" font="default" size="100%">P.B. Hamm</style></author><author><style face="normal" font="default" size="100%">Riley, K.L.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Symptoms and Phytophthora spp. associated with root rot and stem canker of noble fir Christmas trees in the Pacific Northwest</style></title><secondary-title><style face="normal" font="default" size="100%">Plant disease</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Abies procera</style></keyword><keyword><style  face="normal" font="default" size="100%">America</style></keyword><keyword><style  face="normal" font="default" size="100%">Artificial forest stand</style></keyword><keyword><style  face="normal" font="default" size="100%">Coniferales</style></keyword><keyword><style  face="normal" font="default" size="100%">epidemiology</style></keyword><keyword><style  face="normal" font="default" size="100%">Field study</style></keyword><keyword><style  face="normal" font="default" size="100%">Fungi</style></keyword><keyword><style  face="normal" font="default" size="100%">Gymnospermae</style></keyword><keyword><style  face="normal" font="default" size="100%">Host agent relation</style></keyword><keyword><style  face="normal" font="default" size="100%">infection</style></keyword><keyword><style  face="normal" font="default" size="100%">Mycosis</style></keyword><keyword><style  face="normal" font="default" size="100%">North America</style></keyword><keyword><style  face="normal" font="default" size="100%">Oregon</style></keyword><keyword><style  face="normal" font="default" size="100%">Phycomycetes</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytophthora</style></keyword><keyword><style  face="normal" font="default" size="100%">Plant pathogen</style></keyword><keyword><style  face="normal" font="default" size="100%">Root</style></keyword><keyword><style  face="normal" font="default" size="100%">Softwood forest tree</style></keyword><keyword><style  face="normal" font="default" size="100%">Spermatophyta</style></keyword><keyword><style  face="normal" font="default" size="100%">Stem</style></keyword><keyword><style  face="normal" font="default" size="100%">Symptomatology</style></keyword><keyword><style  face="normal" font="default" size="100%">Thallophyta</style></keyword><keyword><style  face="normal" font="default" size="100%">United States</style></keyword><keyword><style  face="normal" font="default" size="100%">Washington</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">1995</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://www.apsnet.org/publications/PlantDisease/BackIssues/Documents/1995Abstracts/PD_79_290.htm</style></url></web-urls></urls><number><style face="normal" font="default" size="100%">3</style></number><publisher><style face="normal" font="default" size="100%">American Phytopathological Society</style></publisher><volume><style face="normal" font="default" size="100%">79</style></volume><pages><style face="normal" font="default" size="100%">290–293</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%">J. M. Davidson</style></author><author><style face="normal" font="default" size="100%">Werres, S.</style></author><author><style face="normal" font="default" size="100%">Garbelotto, M.</style></author><author><style face="normal" font="default" size="100%">Hansen, E.M.</style></author><author><style face="normal" font="default" size="100%">D. M. Rizzo</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Sudden oak death and associated diseases caused by Phytophthora ramorum.</style></title><secondary-title><style face="normal" font="default" size="100%">Plant Management Network - Plant Health Progress</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2003</style></year><pub-dates><date><style  face="normal" font="default" size="100%">July 2003</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://www.plantmanagementnetwork.org/php/shared/sod/</style></url></web-urls></urls><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%">J. M. Davidson</style></author><author><style face="normal" font="default" size="100%">Patterson, H. A.</style></author><author><style face="normal" font="default" size="100%">D. M. Rizzo</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Sources of inoculum for Phytophthora ramorum in a redwood forest</style></title><secondary-title><style face="normal" font="default" size="100%">Phytopathology</style></secondary-title></titles><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://apsjournals.apsnet.org/doi/abs/10.1094/PHYTO-98-8-0860</style></url></web-urls></urls><number><style face="normal" font="default" size="100%">8</style></number><volume><style face="normal" font="default" size="100%">98</style></volume><pages><style face="normal" font="default" size="100%">860-866</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%">EFSA Panel on Plant Health (PLH)</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Scientific opinion on the pest risk analysis on Phytophthora ramorum prepared by the FP6 project RAPRA</style></title><secondary-title><style face="normal" font="default" size="100%">EFSA Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Larix kaempferi</style></keyword><keyword><style  face="normal" font="default" size="100%">management options</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytophthora ramorum</style></keyword><keyword><style  face="normal" font="default" size="100%">ramorum blight</style></keyword><keyword><style  face="normal" font="default" size="100%">RAPRA</style></keyword><keyword><style  face="normal" font="default" size="100%">risk assessment</style></keyword><keyword><style  face="normal" font="default" size="100%">Sudden oak death</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2011</style></year><pub-dates><date><style  face="normal" font="default" size="100%">28 June 2011</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://www.efsa.europa.eu/en/efsajournal/pub/2186.htm</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">9(6)</style></volume><pages><style face="normal" font="default" size="100%">107 pp.</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 Panel on Plant Health was asked to deliver a scientific opinion on the Pest Risk Analysis on &lt;em&gt;Phytophthora ramorum&lt;/em&gt; prepared by the FP6 project RAPRA, taking into account comments by Member States and additional information since RAPRA. &lt;em&gt;P. ramorum&lt;/em&gt; is the oomycete causing sudden oak death in the USA and leaf and twig blight/dieback on a range of ornamental species in North America and Europe. Currently &lt;em&gt;P. ramorum&lt;/em&gt; is not listed as a harmful organism in Council Directive 2000/29/EC, but the Commission adopted in 2002 provisional emergency measures to prevent introduction into and spread within the EU. Recent large-scale outbreaks in Japanese larch (&lt;em&gt;Larix kaempferi&lt;/em&gt;) plantations in the UK and Ireland have worsened the potential consequences in the risk assessment area. However, the Panel concludes that the broad narrative in the RAPRA report stands and supports its conclusion that “There is a risk of further entry (of known or new lineages and/or mating types), establishment and […] impact”. It is advisable to avoid introductions of different lineages because of inherent phenotypic differences and the potential for sexual recombination. The Panel supports the management options proposed in the RAPRA report and adds further measures for consideration. Uncertainty remains over the extent to which the association between control measures and gradual reduction in the number of cases in nurseries is causal. The emergency measures have not prevented outbreaks occurring in the natural environment. The many other remaining uncertainties (fitness of progeny, hybridisation with other &lt;em&gt;Phytophthora&lt;/em&gt; species, host range and epidemiological role of new hosts, early detection of new outbreaks, understanding of long-range dispersal, structure of plant trade networks, origin of the pathogen) call for further research on &lt;em&gt;P. ramorum&lt;/em&gt; across Europe. Regulatory work should keep updated with research results on &lt;em&gt;P. ramorum&lt;/em&gt; and further development of the Japanese larch outbreaks. © European Food Safety Authority, 2011&lt;/p&gt;</style></abstract><section><style face="normal" font="default" size="100%">2186</style></section></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%">Elegbede, Chabi Fabrice</style></author><author><style face="normal" font="default" size="100%">Pierrat, Jean-Claude</style></author><author><style face="normal" font="default" size="100%">Aguayo, Jaime</style></author><author><style face="normal" font="default" size="100%">Husson, Claude</style></author><author><style face="normal" font="default" size="100%">Halkett, Fabien</style></author><author><style face="normal" font="default" size="100%">Beno{\^ıt Mar{\c c}ais</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">A statistical model to detect asymptomatic infectious individuals with an application in the Phytophthora alni-Induced alder decline</style></title><secondary-title><style face="normal" font="default" size="100%">Phytopathology</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">spatial point pattern analysis</style></keyword><keyword><style  face="normal" font="default" size="100%">survival analysis</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/10.1094/PHYTO-05-10-0140</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">100</style></volume><pages><style face="normal" font="default" size="100%">1262-1269</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 some diseases—in particular, tree root infection—stages of infection and inoculum production level and timing are not readily observable because of uncertainty or time lags in symptom appearance. Here, we pose a criterion, based on relative hazard of disease symptoms, to discriminate between healthy and asymptomatic infected individuals. We design a statistical procedure to estimate the criterion for a 6-year survey of alder decline along a northeastern French river. Individual tree symptom hazard was modeled with Cox’s regression model, taking estimation of local infection pressure as a risk factor. From an inoculum production experiment, we thereafter assessed the inoculum production level of target trees, including symptomatic and asymptomatic trees ranked according to their symptoms hazard. Using receiver operating characteristic methods, we first evaluated the criterion performance and determined the discrimination threshold to sort out asymptomatic individuals into healthy and infected. Then, we highlighted the fact that the infected asymptomatic trees were among the major inoculum producers whereas severely declining and dead trees were found to be poor inoculum sources.&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%">Érsek, Tibor</style></author><author><style face="normal" font="default" size="100%">Nagy, Zoltán</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Species hybrids in the genus Phytophthora with emphasis on the alder pathogen Phytophthora alni: a review</style></title><secondary-title><style face="normal" font="default" size="100%">European Journal of Plant Pathology</style></secondary-title></titles><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/10.1007/s10658-008-9296-z</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%">122</style></volume><pages><style face="normal" font="default" size="100%">31-39</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 review provides a summary of recent examples of interspecific hybridisation within the oomycetous genus &lt;em&gt;Phytophthora&lt;/em&gt;. Species hybrids either created in the laboratory or evolved in natural environments are discussed in association with evolutionary issues and possible threats they may pose to agriculture, horticulture and forestry. It is suggested that sustainable control of such hybrids will depend on the better understanding of temporal and spatial aspects of genetic mechanisms and environmental factors that lead to the hybridisation process and thus the genetic diversity in &lt;em&gt;Phytophthora&lt;/em&gt; populations.&lt;/p&gt;</style></abstract><notes><style face="normal" font="default" size="100%">10.1007/s10658-008-9296-z</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%">Fichtner, E. J.</style></author><author><style face="normal" font="default" size="100%">Lynch, S. C.</style></author><author><style face="normal" font="default" size="100%">D. M. Rizzo</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Survival, dispersal, and potential soil-mediated suppression of Phytophthora ramorum in a California redwood-tanoak Forest</style></title><secondary-title><style face="normal" font="default" size="100%">Phytopathology</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://apsjournals.apsnet.org/doi/abs/10.1094/PHYTO-99-5-0608</style></url></web-urls></urls><number><style face="normal" font="default" size="100%">5</style></number><volume><style face="normal" font="default" size="100%">99</style></volume><pages><style face="normal" font="default" size="100%">608-619</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><notes><style face="normal" font="default" size="100%">PMID: 19351257</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%">Susan J. Frankel</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Sudden oak death and Phytophthora ramorum in the USA: a management challenge</style></title><secondary-title><style face="normal" font="default" size="100%">Australasian Plant Pathology</style></secondary-title></titles><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://www.publish.csiro.au/?paper=AP07088</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">37</style></volume><pages><style face="normal" font="default" size="100%">19–25</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Oaks and tanoaks in California and Oregon coastal forests are being ravaged by sudden oak death. The exotic causal agent, &lt;em&gt;Phytophthora ramorum&lt;/em&gt;, is an oomycete in the Straminipile group, a relative of diatoms and algae. &lt;em&gt;P. ramorum&lt;/em&gt; also infects many popular horticultural plants (i.e. camellia and rhododendron), causing ramorum blight, with symptoms expressed as leaf spots, twig blight and shoot dieback. &lt;em&gt;P. ramorum&lt;/em&gt; has raised important biosecurity issues, which continue to reverberate through the agriculture, forestry and horticulture industries as well as associated government management, regulatory and scientific agencies. The continued spread of this and other new &lt;em&gt;Phytophthora&lt;/em&gt; spp. presents significant impetus for adjustments in the management and regulation of forest pathogens and nursery stock.&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, Matteo</style></author><author><style face="normal" font="default" size="100%">Hayden, Katherine J.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Sudden Oak Death: Interactions of the Exotic Oomycete Phytophthora ramorum with Naïve North American Hosts</style></title><secondary-title><style face="normal" font="default" size="100%">Eukaryotic Cell</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://ec.asm.org/content/11/11/1313.abstract</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">1313-1323</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Ten years after a threatening and previously unknown disease of oaks and tanoaks appeared in coastal California, a significant amount of progress has been made toward the understanding of its causal agent &lt;em&gt;Phytophthora ramorum&lt;/em&gt; and of the novel pathosystems associated with this exotic organism. However, a complete understanding of the ecology and epidemiology of this species still eludes us. In part, our inability to fully understand this organism is due to its phylogenetic, phylogeographic, phenotypic, and epidemiological complexities, all reviewed in this paper. Most lines of evidence suggest that the high degree of disease severity reported in California is not simply due to a generalized lack of resistance or tolerance in naïve hosts but also to an innate ability of the pathogen to survive in unfavorable climatic conditions and to reproduce rapidly when conditions become once again favorable.&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, Matteo</style></author><author><style face="normal" font="default" size="100%">Katherine J. Hayden</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Sudden Oak Death: interactions of the exotic oomycete Phytophthora ramorum with naïve North American hosts</style></title><secondary-title><style face="normal" font="default" size="100%">Eukaryotic Cell</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://ec.asm.org/content/early/2012/09/18/EC.00195-12.abstract</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">Early release</style></volume><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Ten years after a threatening and previously unknown disease of oaks and tanoaks appeared in coastal California, a significant amount of progress has been made towards the understanding of its causal agent &lt;em&gt;Phytophthora ramorum&lt;/em&gt; and of the novel pathosystems associated with this exotic organism. However, a complete understanding of the ecology and epidemiology of this species still eludes us. In part, our inability to fully understand this organism is due to its phylogenetic, phylogeographic, phenotypic, and epidemiological complexity, all reviewed in this paper. Most lines of evidence suggest the high disease severity reported in California is not simply due to a generalized lack of resistance or tolerance in na{\&quot;ıve hosts, but also to an innate ability of the pathogen to survive in unfavorable climatic conditions and to reproduce rapidly when conditions become once again favorable.&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%">Gardner, Judy Frances</style></author><author><style face="normal" font="default" size="100%">Dick, Margaret Anne</style></author><author><style face="normal" font="default" size="100%">Bader, Martin Karl-Friedrich</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Susceptibility of New Zealand flora to Phytophthora kernoviae and its seasonal variability in the field</style></title><secondary-title><style face="normal" font="default" size="100%">New Zealand Journal of Forestry Science</style></secondary-title><short-title><style face="normal" font="default" size="100%">N.Z. j. of For. Sci.</style></short-title></titles><dates><year><style  face="normal" font="default" size="100%">2015</style></year><pub-dates><date><style  face="normal" font="default" size="100%">12 November 2015</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://www.nzjforestryscience.com/content/45/1/23</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">45</style></volume><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;div class=&quot;collapsible-content&quot;&gt;&lt;h4&gt;Background&lt;/h4&gt;&lt;p style=&quot;line-height: 160%;&quot;&gt;The oomycete &lt;em&gt;Phytophthora kernoviae&lt;/em&gt; is known from the United Kingdom and the Republic of Ireland, where it is considered to be a recent invader, from Chile where it was only discovered in 2014, and New Zealand where records date back to 1953. As there is little information in New Zealand linking &lt;em&gt;P. kernoviae&lt;/em&gt; with plant disease, it may have been present for much longer and may be indigenous. Seasonal activity of &lt;em&gt;P. kernoviae&lt;/em&gt; in a site known to have infested soil was tested by isolation from soil and foliage of existing shrubs and the use of indicator plants. In greenhouse studies, the susceptibility of a range of indigenous plants to &lt;em&gt;P. kernoviae&lt;/em&gt; was tested via stem and foliar inoculation.&lt;/p&gt;&lt;h4&gt;Methods&lt;/h4&gt;&lt;p style=&quot;line-height: 160%;&quot;&gt;Soil, litter and understorey vegetation samples were collected for isolation of &lt;em&gt;P. kernoviae&lt;/em&gt; at monthly intervals for a year. Plants of &lt;em&gt;Rhododendron catawbiense&lt;/em&gt;, which is known to be susceptible to foliar and shoot infection, were placed in the stand as indicator species. In laboratory and greenhouse studies, stem and foliar inoculations of a selection of arborescent plants representing major groups within the New Zealand flora were carried out and compared with three exotic plants of known susceptibility.&lt;/p&gt;&lt;h4&gt;Results&lt;/h4&gt;&lt;p style=&quot;line-height: 160%;&quot;&gt;&lt;em&gt;Phytophthora kernoviae&lt;/em&gt; was not isolated from foliage of understorey plants at the study site, but it was recovered from soil and litter from April to November (autumn through spring) inclusive. Little disease developed on the &lt;em&gt;Rhododendron catawbiense&lt;/em&gt; indicator plants.&lt;/p&gt;&lt;p style=&quot;line-height: 160%;&quot;&gt;All of the exotic, and most of the indigenous, species developed a lesion in response to stem inoculation. Stem lesions were more developed on exotic species than on indigenous hosts. In contrast, few species formed foliar symptoms. &lt;em&gt;Phytophthora kernoviae&lt;/em&gt; was recovered from asymptomatic tissue, stems and foliage, of a number of species.&lt;/p&gt;&lt;h4&gt;Conclusions&lt;/h4&gt;&lt;p style=&quot;line-height: 160%;&quot;&gt;Based on the results of the inoculations and the lack of historical records of disease of indigenous plants associated with &lt;em&gt;P. kernoviae&lt;/em&gt;, this oomycete does not appear to be a damaging pathogen of New Zealand’s indigenous flora. Although presence in the soil or litter was demonstrated at the study site, little disease developed on the indicator plants suggesting that at least part of the New Zealand population is of low pathogenicity to &lt;em&gt;R. catawbiense.&lt;/em&gt;&lt;/p&gt;&lt;/div&gt;</style></abstract><section><style face="normal" font="default" size="100%">23</style></section></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%">Goheen, E. M.</style></author><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%">McWilliams, M.G.</style></author><author><style face="normal" font="default" size="100%">Osterbauer, N.</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%">Sudden oak death caused by Phytophthora ramorum in Oregon</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%">2002</style></year><pub-dates><date><style  face="normal" font="default" size="100%">04/2002</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1094/PDIS.2002.86.4.441C</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">86</style></volume><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Sudden oak death, caused by &lt;em&gt;Phytophthora ramorum&lt;/em&gt; (1,2), has been found for the first time in Oregon, killing tanoak, &lt;em&gt;Lithocarpus densiflorus&lt;/em&gt;, trees. To our knowledge, this is the first report of the disease outside of the San Francisco to Monterey area in California, (300 km to the south). Nine areas of infestation, all within a 24-km&lt;sup&gt;2&lt;/sup&gt; area, were discovered on forest lands near Brookings, in southwest Oregon. Mortality centers ranged in size from 0.2 to 4.5 ha and included 5 to approximately 40 diseased trees. &lt;em&gt;P. ramorum&lt;/em&gt; was isolated from stem cankers using &lt;em&gt;Phytophthora&lt;/em&gt;-selective medium. Isolates had distinctive morphological features characteristic of &lt;em&gt;P. ramorum&lt;/em&gt;, including abundant production of chlamydospores and caducous, semipapillate sporangia on solid media. Internal transcribed spacer (ITS) sequences of isolates of &lt;em&gt;P. ramorum&lt;/em&gt; from Oregon were identical to ITS sequences of isolates from California (1). The pathogen also was isolated from necrotic lesions on leaves and stems of native &lt;em&gt;Rhododendron macrophyllum&lt;/em&gt; and &lt;em&gt;Vaccinium ovatum&lt;/em&gt; growing beneath diseased tanoaks. In July 2001, the disease was located by an aerial survey conducted cooperatively by the USDA Forest Service and Oregon Department of Forestry. All lands within 1.6 km (1 mile) of the mortality centers are subject to Oregon quarantine, which bars the transport of any host plant materials. An eradication effort is currently underway. Symptomatic plants and all known host plants within 15 to 30 m of symptomatic plants are being cut and burned in the first phase of this operation. The total treated area is approximately 16 ha.&lt;/p&gt;</style></abstract><section><style face="normal" font="default" size="100%">441</style></section></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%">Goss, Erica M.</style></author><author><style face="normal" font="default" size="100%">Ivors, Kelly</style></author><author><style face="normal" font="default" size="100%">Garbelotto, Matteo</style></author><author><style face="normal" font="default" size="100%">Martin, Frank N.</style></author><author><style face="normal" font="default" size="100%">Prospero, Simone</style></author><author><style face="normal" font="default" size="100%">Everett Hansen</style></author><author><style face="normal" font="default" size="100%">Peter J.M. Bonants</style></author><author><style face="normal" font="default" size="100%">Hamelin, Richard C.</style></author><author><style face="normal" font="default" size="100%">Chastagner, Gary</style></author><author><style face="normal" font="default" size="100%">Werres, Sabine</style></author><author><style face="normal" font="default" size="100%">Rizzo, David M.</style></author><author><style face="normal" font="default" size="100%">Abad, Gloria</style></author><author><style face="normal" font="default" size="100%">Beales, Paul</style></author><author><style face="normal" font="default" size="100%">Bilodeau, Guillaume J.</style></author><author><style face="normal" font="default" size="100%">Cheryl L. Blomquist</style></author><author><style face="normal" font="default" size="100%">Brasier,Clive</style></author><author><style face="normal" font="default" size="100%">Brière, Stephan C.</style></author><author><style face="normal" font="default" size="100%">Chandelier, Anne</style></author><author><style face="normal" font="default" size="100%">Davidson, Jennifer M.</style></author><author><style face="normal" font="default" size="100%">Denman,Sandra</style></author><author><style face="normal" font="default" size="100%">Elliott, Marianne</style></author><author><style face="normal" font="default" size="100%">Susan J. Frankel</style></author><author><style face="normal" font="default" size="100%">Goheen, Ellen M.</style></author><author><style face="normal" font="default" size="100%">de Gruyter, Hans</style></author><author><style face="normal" font="default" size="100%">Heungens, Kurt</style></author><author><style face="normal" font="default" size="100%">James, Delano</style></author><author><style face="normal" font="default" size="100%">Kanaskie, Alan</style></author><author><style face="normal" font="default" size="100%">Michael G McWilliams</style></author><author><style face="normal" font="default" size="100%">Man in ‘t Veld, Willem</style></author><author><style face="normal" font="default" size="100%">Moralejo, Eduardo</style></author><author><style face="normal" font="default" size="100%">Osterbauer, Nancy K.</style></author><author><style face="normal" font="default" size="100%">Palm, Mary E.</style></author><author><style face="normal" font="default" size="100%">Parke, Jennifer L.</style></author><author><style face="normal" font="default" size="100%">Sierra, Ana Maria Perez</style></author><author><style face="normal" font="default" size="100%">Shamoun, Simon F.</style></author><author><style face="normal" font="default" size="100%">Shishkoff, Nina</style></author><author><style face="normal" font="default" size="100%">Tooley, Paul W.</style></author><author><style face="normal" font="default" size="100%">Vettraino, Anna Maria</style></author><author><style face="normal" font="default" size="100%">Webber,Joan</style></author><author><style face="normal" font="default" size="100%">Timothy L. Widmer</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Standardizing the nomenclature for clonal lineages of the sudden oak death pathogen, Phytophthora ramorum</style></title><secondary-title><style face="normal" font="default" size="100%">Phytopathology</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://apsjournals.apsnet.org/doi/abs/10.1094/PHYTO-99-7-0792</style></url></web-urls></urls><number><style face="normal" font="default" size="100%">7</style></number><volume><style face="normal" font="default" size="100%">99</style></volume><pages><style face="normal" font="default" size="100%">792-795</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;, the causal agent of sudden oak death and &lt;em&gt;ramorum&lt;/em&gt; blight, is known to exist as three distinct clonal lineages which can only be distinguished by performing molecular marker-based analyses. However, in the recent literature there exists no consensus on naming of these lineages. Here we propose a system for naming clonal lineages of &lt;em&gt;P. ramorum&lt;/em&gt; based on a consensus established by the &lt;em&gt;P. ramorum&lt;/em&gt; research community. Clonal lineages are named with a two letter identifier for the continent on which they were first found (e.g.&lt;/p&gt;</style></abstract><notes><style face="normal" font="default" size="100%">PMID: 19522576</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%">Hansen, E.M.</style></author><author><style face="normal" font="default" size="100%">D. P. Maxwell</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Species of the Phytophthora megasperma complex</style></title><secondary-title><style face="normal" font="default" size="100%">Mycologia,</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">1991</style></year><pub-dates><date><style  face="normal" font="default" size="100%">May - Jun., 1991</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://www.jstor.org/stable/3759999</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">83</style></volume><pages><style face="normal" font="default" size="100%">376-381</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%">Hansen, E.M.</style></author><author><style face="normal" font="default" size="100%">P.B. Hamm</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Survival of Phytophthora lateralis in infected roots of Port Orford cedar</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%">1996</style></year></dates><number><style face="normal" font="default" size="100%">9</style></number><publisher><style face="normal" font="default" size="100%">[St. Paul, Minn.: American Phytopathological Society], 1980-</style></publisher><volume><style face="normal" font="default" size="100%">80</style></volume><pages><style face="normal" font="default" size="100%">1075–1078</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%">Hansen, E.M.</style></author><author><style face="normal" font="default" size="100%">Parke, J. L.</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%">Susceptibility of Oregon forest trees and shrubs to Phytophthora ramorum: a comparison of artificial inoculation and natural infection</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%">2005</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://apsjournals.apsnet.org/doi/abs/10.1094/PD-89-0063</style></url></web-urls></urls><number><style face="normal" font="default" size="100%">1</style></number><volume><style face="normal" font="default" size="100%">89</style></volume><pages><style face="normal" font="default" size="100%">63-70</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; is an invasive pathogen in some mixed-hardwood forests in California and southwestern Oregon, where it causes sudden oak death (SOD) on some members of &lt;em&gt;Fagaceae, ramorum&lt;/em&gt; shoot dieback on some members of &lt;em&gt;Ericaceae&lt;/em&gt; and conifers, and &lt;em&gt;ramorum&lt;/em&gt; leaf blight on diverse hosts. We compared symptoms of &lt;em&gt;P. ramorum&lt;/em&gt; infection resulting from four different artificial inoculation techniques with the symptoms of natural infection on 49 western forest trees and shrubs; 80% proved susceptible to one degree or another. No single inoculation method predicted the full range of symptoms observed in the field, but whole plant dip came closest. Detached-leaf-dip inoculation provided a rapid assay and permitted a reasonable assessment of susceptibility to leaf blight. Both leaf age and inoculum dose affected detached-leaf assays. SOD and dieback hosts often developed limited leaf symptoms, although the pattern of midrib and petiole necrosis was distinctive. Stem-wound inoculation of seedlings correlated with field symptoms for several hosts. The results suggested that additional conifer species may be damaged in the field. Log inoculation provided a realistic test of susceptibility to SOD, but was cumbersome and subject to seasonal variability. Pacific rhododendron, salmonberry, cascara, and poison oak were confirmed as hosts by completing Koch’s postulates. Douglas-fir was most susceptible to shoot dieback shortly after budburst, with infection occurring at the bud.&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%">L.F. Roth</style></author><author><style face="normal" font="default" size="100%">P.B. Hamm</style></author><author><style face="normal" font="default" size="100%">A. J. Julis.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Survival, spread, and pathogenicity of Phytophthora spp. on Douglas-fir seedlings planted on forest sites.</style></title><secondary-title><style face="normal" font="default" size="100%">Phytopathology 70:</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">1980</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://www.apsnet.org/publications/phytopathology/backissues/Documents/1980Abstracts/Phyto70_422.htm</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">70</style></volume><pages><style face="normal" font="default" size="100%">422-425</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Douglas-fir seedling stock infected in the nursery with &lt;em&gt;Phytophthora cryptogea, P. drechsleri, P. megasperma, P. cactorum&lt;/em&gt;, and an unidentified &lt;em&gt;Phytophthora sp&lt;/em&gt;. were outplanted on commercial forest sites to test survival of the diseased trees and of the pathogens. Mortality of trees initially classified in severe, moderate, and inconspicuous symptom classes at outplanting reached 61, 26, and 11%, respectively, after 18 mo. &lt;em&gt;Phytophthora&lt;/em&gt; was recovered about equally from roots of trees in each symptom class (15, 13, and 12%). Surviving trees regenerated healthy roots above old lesions even though &lt;em&gt;Phytophthora&lt;/em&gt; persisted. Disease spread was limited. None of 360 healthy trees planted 0.6 m downslope from diseased trees became infected, and only 2 of 720 healthy trees became infected after each was paired with a diseased tree in the same planting hole.&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%">Harris, A. R.</style></author><author><style face="normal" font="default" size="100%">Webber, J. F.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Sporulation potential, symptom expression and detection of Phytophthora ramorum on larch needles and other foliar hosts</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%">2016</style></year><pub-dates><date><style  face="normal" font="default" size="100%">Jan-12-2016</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1111/ppa.12538 </style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">65</style></volume><pages><style face="normal" font="default" size="100%">1441 - 1451</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; has caused extensive dieback and mortality of commercially grown Japanese larch (&lt;em&gt;Larix kaempferi&lt;/em&gt;) in many parts of the UK, as infected foliage generates spores that then cause bark lesions and girdling cankers on trees. Following inoculation, individual needles of Japanese, European (&lt;em&gt;L.&amp;nbsp;decidua&lt;/em&gt;) and hybrid (&lt;em&gt;L.&amp;nbsp;&lt;/em&gt;×&amp;nbsp;&lt;em&gt;eurolepis&lt;/em&gt;) larch infected with &lt;em&gt;P.&amp;nbsp;ramorum&lt;/em&gt; can produce thousands of sporangia. Mean numbers of sporangia ranged from 806 to 1778 per cm&lt;sup&gt;2&lt;/sup&gt; (hybrid larch and Japanese larch, respectively), surpassing mean sporulation levels on foliar hosts previously associated with &lt;em&gt;P.&amp;nbsp;ramorum&lt;/em&gt; outbreaks in Britain, namely &lt;em&gt;Rhododendron ponticum&lt;/em&gt;,&lt;em&gt; Castanea sativa&lt;/em&gt; and &lt;em&gt;Vaccinium myrtillus&lt;/em&gt;. Sporulation on larch even exceeded that of California bay laurel (&lt;em&gt;Umbellularia californica&lt;/em&gt;), which drives the sudden oak death epidemic in California. Inoculation of foliage selected at different times of year revealed that foliage age significantly affected sporulation levels, but this varied with host species. However, symptom development and sporulation were often not correlated. Symptoms on larch were frequently insignificant or even absent at certain times of year, with sometimes the only evidence of infection being the emergence of sporangia from needles, without any sign of discolouration or necrosis. Plating infected but symptomless needles onto &lt;em&gt;Phytophthora&lt;/em&gt; selective medium also often failed to yield the pathogen. Symptomless infection of larch needles apparently occurs, but is only detectable with microscopy. More generally, it is suggested that diagnosis of &lt;em&gt;Phytophthora&lt;/em&gt; infection in conifers is often underestimated due to isolation difficulties and delayed symptom expression.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">9</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%">Hislop, E. C.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Studies on the chemical control of Phytophthora palmivora (Butl.) Butl. on Theobroma cacao L. in Nigeria.</style></title><secondary-title><style face="normal" font="default" size="100%">Annals of Applied Biology</style></secondary-title><short-title><style face="normal" font="default" size="100%">Ann Applied Biology</style></short-title></titles><dates><year><style  face="normal" font="default" size="100%">1963</style></year><pub-dates><date><style  face="normal" font="default" size="100%">12/1963</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://onlinelibrary.wiley.com/doi/10.1111/j.1744-7348.1963.tb03770.x/abstract;jsessionid=FA42764CD24DC2258C2776AF065DAB4F.d01t01</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">52</style></volume><pages><style face="normal" font="default" size="100%">465 - 480</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;div class=&quot;para&quot;&gt;&lt;p&gt;In laboratory trials, phenyl mercury nitrate at 0·02 p.p.m. and fentin acetate at 0·2 p.p.m. severely retarded growth of four isolates of &lt;em&gt;Phytophthora palmivora&lt;/em&gt; on cassava agar. These two chemicals, with captan, maneb and a dithiocarbamate-copper chelate, were also highly toxic to encysted zoospores of a ‘rubber’ group isolate of &lt;em&gt;P. palmivora.&lt;/em&gt;&lt;/p&gt;&lt;/div&gt;&lt;div class=&quot;para&quot;&gt;&lt;p&gt;Deposits of captan on pods were readily removed by artificial rain, but some improvement in tenacity was obtained by the addition of a sticker. In other laboratory trials, the deposit from low-volume sprays of cuprous oxide dried more quickly on pods than that from high-volume sprays but showed no advantage in subsequent resistance to weathering.&lt;/p&gt;&lt;/div&gt;&lt;div class=&quot;para&quot;&gt;&lt;p&gt;In a field trial in 1961, seven fungicide treatments were applied three-weekly and compared with an unsprayed control. The lowest percentage black-pod infection followed treatment with fentin acetate: Bordeaux mixture and carbide Bordeaux both gave good control. The captan treatments were completely ineffective. More black pods were harvested from close-spaced trees than from those wide-spaced.&lt;/p&gt;&lt;/div&gt;&lt;div class=&quot;para&quot;&gt;&lt;p&gt;Weekly applications of 0·15% fentin acetate to seedlings induced no significant damage.&lt;/p&gt;&lt;/div&gt;&lt;div class=&quot;para&quot;&gt;&lt;p&gt;In a field trial made in 1962 very heavy rainfall provided a severe test of the fungicides, the most effective being Bordeaux mixture and carbide Bordeaux mixture applied three-weekly, carbide Bordeaux mixture applied four-weekly and fentin acetate applied two-weekly. Captan with added sticker was again no better than the control. There was no marked effect of spacing.&lt;/p&gt;&lt;/div&gt;&lt;div class=&quot;para&quot;&gt;&lt;p&gt;Comparisons of Bordeaux and carbide Bordeaux mixtures made at two other sites in 1962 showed no difference in disease control. It is suggested that carbide Bordeaux mixture could be replaced by the cheaper preparation made with lime.&lt;/p&gt;&lt;/div&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%">Ho, HH</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Synoptic keys to the species of Phytophthora</style></title><secondary-title><style face="normal" font="default" size="100%">Mycologia</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">1981</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://www.jstor.org/stable/3759497</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">Mycological Society of America</style></publisher><volume><style face="normal" font="default" size="100%">73</style></volume><pages><style face="normal" font="default" size="100%">705-714</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Three synoptic keys to the species of &lt;em&gt;Phytophthora&lt;/em&gt; are presented to facilitate identification of, respectively, the plant pathogenic species in culture, the plant pathogenic species known only on hosts, and the aquatic species.&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%">Renaud Ioos</style></author><author><style face="normal" font="default" size="100%">Husson, Claude</style></author><author><style face="normal" font="default" size="100%">Axelle Andrieux</style></author><author><style face="normal" font="default" size="100%">Pascal Frey</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">SCAR–based PCR primers to detect the hybrid pathogen Phytophthora alni and its subspecies causing alder disease in Europe</style></title><secondary-title><style face="normal" font="default" size="100%">European Journal of Plant Pathology</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2005</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1007/s10658-005-6233-2</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%">112</style></volume><pages><style face="normal" font="default" size="100%">323-335</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Since the 1990s, a new &lt;em&gt;Phytophthora&lt;/em&gt; species hybrid has been jeopardizing the natural population of alders throughout Europe. This new &lt;em&gt;Phytophthora, P. alni&lt;/em&gt;, has been suggested as a natural hybrid between two closely related species of &lt;em&gt;Phytophthora&lt;/em&gt;. Little is known about the epidemiology of this pathogen, because its direct isolation is not always satisfactory. In this study we developed three pairs of Polymerase Chain Reaction (PCR) primers derived from Sequence Characterized Amplified Regions (SCAR) that allow discrimination among the three subspecies of &lt;em&gt;P. alni: P. alni subsp. alni, P. alni subsp. uniformis&lt;/em&gt; and &lt;em&gt;P. alni subsp. multiformis&lt;/em&gt;. These molecular tools were successfully used to detect &lt;em&gt;P. alni&lt;/em&gt; directly in different substrates such as infested river water and soil, and necrotic alder bark, without the need for any prior baiting or isolation stages. An Internal Amplification Control (IAC) was included to help discriminate against false negative samples due to the potential presence of inhibitory compounds in DNA extracts. These molecular tools should be useful for epidemiological studies on this emerging disease.&lt;/p&gt;</style></abstract><notes><style face="normal" font="default" size="100%">10.1007/s10658-005-6233-2</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%">Jules, Erik S.</style></author><author><style face="normal" font="default" size="100%">Kauffman, Matthew J.</style></author><author><style face="normal" font="default" size="100%">Ritts, William D.</style></author><author><style face="normal" font="default" size="100%">Carroll, Allyson L.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Spread of an invasive pathogen over a variable landscape: a non-native root rot on Port Orford cedar</style></title><secondary-title><style face="normal" font="default" size="100%">Ecology</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2002</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://www.esajournals.org/doi/abs/10.1890/0012-9658%282002%29083%5B3167%3ASOAIPO%5D2.0.CO%3B2</style></url></web-urls></urls><number><style face="normal" font="default" size="100%">11</style></number><volume><style face="normal" font="default" size="100%">83</style></volume><pages><style face="normal" font="default" size="100%">3167-3181</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%">Jung, Thomas</style></author><author><style face="normal" font="default" size="100%">Scanu, Bruno</style></author><author><style face="normal" font="default" size="100%">Brasier, Clive M.</style></author><author><style face="normal" font="default" size="100%">Webber, Joan</style></author><author><style face="normal" font="default" size="100%">Milenković, Ivan</style></author><author><style face="normal" font="default" size="100%">Corcobado, Tamara</style></author><author><style face="normal" font="default" size="100%">Tomšovský, Michal</style></author><author><style face="normal" font="default" size="100%">Pánek, Matěj</style></author><author><style face="normal" font="default" size="100%">Bakonyi, Jozsef</style></author><author><style face="normal" font="default" size="100%">Maia, Cristiana</style></author><author><style face="normal" font="default" size="100%">Bačová, Aneta</style></author><author><style face="normal" font="default" size="100%">Raco, Milica</style></author><author><style face="normal" font="default" size="100%">Rees, Helen</style></author><author><style face="normal" font="default" size="100%">Pérez-Sierra, Ana</style></author><author><style face="normal" font="default" size="100%">Horta Jung, Marilia</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">A Survey in Natural Forest Ecosystems of Vietnam Reveals High Diversity of both New and Described Phytophthora Taxa including P. ramorum</style></title><secondary-title><style face="normal" font="default" size="100%">Forests</style></secondary-title><short-title><style face="normal" font="default" size="100%">Forests</style></short-title></titles><dates><year><style  face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">Jan-01-2020</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://www.mdpi.com/1999-4907/11/1/93https://www.mdpi.com/1999-4907/11/1/93/pdf</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">93</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;div class=&quot;page&quot; title=&quot;Page 1&quot;&gt;&lt;div class=&quot;layoutArea&quot;&gt;&lt;div class=&quot;column&quot;&gt;&lt;p&gt;In 2016 and 2017, surveys of &lt;em&gt;Phytophthora&lt;/em&gt; diversity were performed in 25 natural and semi-natural forest stands and 16 rivers in temperate and subtropical montane and tropical lowland regions of Vietnam. Using baiting assays from soil samples and rivers and direct isolations from naturally fallen leaves, 13 described species, five informally designated taxa and 21 previously unknown taxa of &lt;em&gt;Phytophthora&lt;/em&gt; were isolated from 58 of the 91 soil samples (63.7%) taken from the rhizosphere of 52 of the 64 woody plant species sampled (81.3%) in 20 forest stands (83.7%), and from all rivers: &lt;em&gt;P. capensis, P. citricola&lt;/em&gt; VII, VIII, IX, X and XI, &lt;em&gt;P.&lt;/em&gt; sp. botryosa-like 2, &lt;em&gt;P.&lt;/em&gt; sp. meadii-like 1 and 2, &lt;em&gt;P.&lt;/em&gt; sp. tropicalis-like 2 and &lt;em&gt;P.&lt;/em&gt; sp. multivesiculata-like 1 from &lt;em&gt;Phytophthora&lt;/em&gt; major phylogenetic Clade 2; &lt;em&gt;P. castaneae&lt;/em&gt; and &lt;em&gt;P. heveae&lt;/em&gt; from Clade 5; &lt;em&gt;P. chlamydospora, P. gregata, P.&lt;/em&gt; sp. bitahaiensis-like and &lt;em&gt;P.&lt;/em&gt; sp. sylvatica-like 1, 2 and 3 from Clade 6; &lt;em&gt;P. cinnamomi&lt;/em&gt; (Pc), &lt;em&gt;P. parvispora, P. attenuata, P.&lt;/em&gt; sp. attenuata-like 1, 2 and 3 and &lt;em&gt;P.&lt;/em&gt; ×heterohybrida from Clade 7; &lt;em&gt;P. drechsleri, P. pseudocryptogea, P. ramorum&lt;/em&gt; (Pr) and &lt;em&gt;P.&lt;/em&gt; sp. kelmania from Clade 8, P. macrochlamydospora, &lt;em&gt;P.&lt;/em&gt; sp. ×insolita-like, &lt;em&gt;P.&lt;/em&gt; sp. ×kunnunara-like, &lt;em&gt;P.&lt;/em&gt; sp. ×virginiana-like s.l. and three new taxa, &lt;em&gt;P.&lt;/em&gt; sp. quininea-like, &lt;em&gt;P.&lt;/em&gt; sp. ×Grenada 3-like and &lt;em&gt;P.&lt;/em&gt; sp. ×Peru 4-like, from Clade 9; and &lt;em&gt;P.&lt;/em&gt; sp. gallica-like 1 and 2 from Clade 10. The A1 and A2 mating types of both Pc and Pr co-occurred. The A2 mating type of Pc was associated with severe dieback of montane forests in northern Vietnam. Most other &lt;em&gt;Phytophthora&lt;/em&gt; species, including Pr, were not associated with obvious disease symptoms. It is concluded that (1) Vietnam is within the center of origin of most &lt;em&gt;Phytophthora&lt;/em&gt; taxa found including Pc and Pr, and (2) &lt;em&gt;Phytophthora&lt;/em&gt; clades 2, 5, 6, 7, 8, 9, and 10 are native to Indochina.&lt;/p&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;</style></abstract><issue><style face="normal" font="default" size="100%">1</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%">John T. Kliejunas</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Sudden oak death and Phytophthora ramorum: a summary of the literature</style></title></titles><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://www.treesearch.fs.fed.us/pubs/36591</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">U.S. Department of Agriculture, Forest Service, Pacific Southwest Research Station.</style></publisher><pub-location><style face="normal" font="default" size="100%">Albany, CA, USA</style></pub-location><pages><style face="normal" font="default" size="100%">181 p.</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%">Kong, Ping</style></author><author><style face="normal" font="default" size="100%">Lea-Cox, John D.</style></author><author><style face="normal" font="default" size="100%">Moorman, Gary W.</style></author><author><style face="normal" font="default" size="100%">Hong, Chuanxue</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Survival of Phytophthora alni, Phytophthora kernoviae, and Phytophthora ramorum in a simulated aquatic environment at different levels of pH</style></title><secondary-title><style face="normal" font="default" size="100%">FEMS Microbiology Letters</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">quarantine Phytophthora species</style></keyword><keyword><style  face="normal" font="default" size="100%">water pH</style></keyword><keyword><style  face="normal" font="default" size="100%">zoospore survival</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2012</style></year><pub-dates><date><style  face="normal" font="default" size="100%">07/2012</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1111/j.1574-6968.2012.02574.x</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">332</style></volume><pages><style face="normal" font="default" size="100%">54–60</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;, &lt;em&gt;Phytophthora alni&lt;/em&gt;, and &lt;em&gt;Phytophthora kernoviae&lt;/em&gt; present significant threats to biosecurity. As zoosporic oomycetes, these plant pathogens may spread through natural waterways and irrigation systems. However, survival of these pathogens in aquatic systems in response to water quality is not well understood. In this study, we investigated their zoospore survival at pH 3–11 in a 10% Hoagland’s solution over a 14-day period. The results showed that all three pathogens were most stable at pH 7, although the populations declined overnight irrespective of pH. Extended survival of these species depended on the tolerance of pH of their germinants. Germinants of &lt;em&gt;P.&amp;nbsp;alni&lt;/em&gt; ssp.&amp;nbsp;&lt;em&gt;alni&lt;/em&gt; and &lt;em&gt;P.&amp;nbsp;ramorum&lt;/em&gt; were more basic tolerant (pH 5–11), while those of &lt;em&gt;P.&amp;nbsp;kernoviae&lt;/em&gt; were more acidic tolerant (pH 3–9). These tolerant germinants formed compact hyphae or secondary sporangia to allow longer survival of these pathogens. Long-term survival at a broad pH range suggests that these pathogens, especially &lt;em&gt;P.&amp;nbsp;ramorum&lt;/em&gt;, are adapted to an aquatic environment and pose a threat to new production areas through water dispersal.&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%">La Manna, L.</style></author><author><style face="normal" font="default" size="100%">Collantes, M.</style></author><author><style face="normal" font="default" size="100%">Bava, J.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Seedling recruitment of Austrocedrus chilensis in relation to cattle use, microsite environment and forest disease</style></title><secondary-title><style face="normal" font="default" size="100%">Ecologia Austral.(Abr</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2008</style></year></dates><number><style face="normal" font="default" size="100%">1</style></number><volume><style face="normal" font="default" size="100%">18</style></volume><pages><style face="normal" font="default" size="100%">27–41</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%">Leonberger, A. J.</style></author><author><style face="normal" font="default" size="100%">Speers, C.</style></author><author><style face="normal" font="default" size="100%">Ruhl, G.</style></author><author><style face="normal" font="default" size="100%">Creswell, T.</style></author><author><style face="normal" font="default" size="100%">Beckerman, J. L.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">A survey of Phytophthora spp. in midwest nurseries, greenhouses, and landscapes</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%">2013</style></year><pub-dates><date><style  face="normal" font="default" size="100%">05/2013</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">97</style></volume><pages><style face="normal" font="default" size="100%">635 - 640</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;A survey of nurseries, greenhouses, and landscapes was conducted from 2006 to 2008 in order to determine the prevalence and diversity of &lt;em&gt;Phytophthora&lt;/em&gt; spp. From sites in Iowa, Michigan, Ohio, and, predominantly, Indiana, 121 &lt;em&gt;Phytophthora&lt;/em&gt; isolates were obtained from 1,657 host samples spanning 32 host genera. Based on sequence of the internal transcribed spacer (ITS) region of the ribosomal DNA, 11 &lt;em&gt;Phytophthora&lt;/em&gt; spp. and two hybrid species were identified. A majority of the isolates were &lt;em&gt;P. citricola&lt;/em&gt; (35.9%) or &lt;em&gt;P. citrophthora&lt;/em&gt; (27.4%). Six isolates were confirmed as hybrids (four of &lt;em&gt;P. cactorum&lt;/em&gt; × &lt;em&gt;hedraiandra&lt;/em&gt; and two of &lt;em&gt;P. nicotianae&lt;/em&gt; × &lt;em&gt;cactorum&lt;/em&gt;) by cloning and sequencing the ITS region. Three &lt;em&gt;P. cactorum&lt;/em&gt; × &lt;em&gt;hedraiandra&lt;/em&gt; isolates were obtained from the same site, from three &lt;em&gt;Rhododendron&lt;/em&gt; spp., which are known hosts to the parental species. The fourth isolate, however, was recovered out of a different location in a &lt;em&gt;Dicentra&lt;/em&gt; sp., which is not a known host to either parental species, suggesting an expansion of host range of the hybrid isolate as compared with either parental species.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">5</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%">Moralejo, Eduardo</style></author><author><style face="normal" font="default" size="100%">Miquel Puig</style></author><author><style face="normal" font="default" size="100%">Jose A. Garcia</style></author><author><style face="normal" font="default" size="100%">Enrique Descals</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Stromata, sporangiomata and chlamydosori of Phytophthora ramorum on inoculated Mediterranean woody plants</style></title><secondary-title><style face="normal" font="default" size="100%">Mycological Research</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Sporangial dispersal</style></keyword></keywords><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.sciencedirect.com/science/article/pii/S0953756206002656</style></url></web-urls></urls><number><style face="normal" font="default" size="100%">11</style></number><volume><style face="normal" font="default" size="100%">110</style></volume><pages><style face="normal" font="default" size="100%">1323 - 1332</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Three types of multihyphal structures, stromata, sporangiomata and chlamydosori, are described for the plant pathogen &lt;em&gt;Phytophthora ramorum&lt;/em&gt;. Their morphology, morphogenesis and position on the host organ were observed by dissecting, compound and scanning electron microscopy. Stromata were consistently formed one to two weeks after zoospore inoculation of detached leaves and fruits of an assortment of Mediterranean sclerophyll shrubs. Stroma initials appeared subcuticularly or subepidermally and developed as small hyphal aggregates by repeated branching, budding, swelling and interweaving, eventually forming a prosenchyma. They always emerged through the adaxial side of the leaf by rupture of the overlying host tissue. Occasionally sporangia and chlamydosori (packed clusters of chlamydospores) were formed on the stromata. Sporangiomata bore short sporangiophores and clusters of 20-100 sporangia and resembled sporodochia of the mitosporic fungi. The biological significance of these multihyphal structures is discussed. Some epidemiological aspects were also studied: several understorey species of the holm oak (&lt;em&gt;Quercus ilex&lt;/em&gt;) woodland were susceptible to in vitro infection with three isolates of &lt;em&gt;P. ramorum&lt;/em&gt; originally collected from different ornamental hosts. The risk of spread to this ecosystem is evaluated.&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%">Murray, Marion S.</style></author><author><style face="normal" font="default" size="100%">Hansen, Everett M.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Susceptibility of Pacific Yew to Phytophthora lateralis</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%">1997</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://apsjournals.apsnet.org/doi/abs/10.1094/PDIS.1997.81.12.1400</style></url></web-urls></urls><number><style face="normal" font="default" size="100%">12</style></number><volume><style face="normal" font="default" size="100%">81</style></volume><pages><style face="normal" font="default" size="100%">1400-1404</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%">Nelson, A.H.</style></author><author><style face="normal" font="default" size="100%">G. W. Hudler</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">A summary of North American hardwood tree diseases with bleeding canker symptoms</style></title><secondary-title><style face="normal" font="default" size="100%">Arboriculture and Urban Forestry </style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2007</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://www.google.com/url?sa=t&amp;rct=j&amp;q=&amp;esrc=s&amp;source=web&amp;cd=57&amp;ved=0CE4QFjAGODI&amp;url=http%3A%2F%2Fjoa.isa-arbor.com%2Frequest.asp%3FJournalID%3D1%26ArticleID%3D2985%26Type%3D2&amp;ei=pKOvUpvjGcv7oASXoYDYDA&amp;usg=AFQjCNHxNzEH7As_NfGpUf1LVGxbCXIeXA</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">33(2)</style></volume><pages><style face="normal" font="default" size="100%">122-131</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%">Oh, Eunsung</style></author><author><style face="normal" font="default" size="100%">Gryzenhout, Marieka</style></author><author><style face="normal" font="default" size="100%">Wingfield, Brenda D.</style></author><author><style face="normal" font="default" size="100%">Wingfield, Michael J.</style></author><author><style face="normal" font="default" size="100%">Burgess, Treena I.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Surveys of soil and water reveal a goldmine of Phytophthora diversity in South African natural ecosystems</style></title><secondary-title><style face="normal" font="default" size="100%">IMA Fungus</style></secondary-title><short-title><style face="normal" font="default" size="100%">imafungus</style></short-title></titles><dates><year><style  face="normal" font="default" size="100%">2013</style></year><pub-dates><date><style  face="normal" font="default" size="100%">Jun-06-2015</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://www.imafungus.org/Issue/41/22.pdf</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">4</style></volume><pages><style face="normal" font="default" size="100%">123 - 131</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;div class=&quot;page&quot; title=&quot;Page 1&quot;&gt;&lt;div class=&quot;section&quot;&gt;&lt;div class=&quot;layoutArea&quot;&gt;&lt;div class=&quot;column&quot;&gt;&lt;p&gt;&lt;span style=&quot;font-size: 8.000000pt; font-family: 'Arial'; font-style: italic;&quot;&gt;Phytophthora &lt;/span&gt;&lt;span style=&quot;font-size: 8.000000pt; font-family: 'ArialMT';&quot;&gt;species are well-known as destructive plant pathogens, especially in natural ecosystems. It is ironic, therefore, how little is known regarding the &lt;/span&gt;&lt;span style=&quot;font-size: 8.000000pt; font-family: 'Arial'; font-style: italic;&quot;&gt;Phytophthora &lt;/span&gt;&lt;span style=&quot;font-size: 8.000000pt; font-family: 'ArialMT';&quot;&gt;diversity in South African natural woody ecosystems. In this study, &lt;/span&gt;&lt;span style=&quot;font-size: 8.000000pt; font-family: 'Arial'; font-style: italic;&quot;&gt;Phytophthora &lt;/span&gt;&lt;span style=&quot;font-size: 8.000000pt; font-family: 'ArialMT';&quot;&gt;species were isolated using standard baiting techniques from 182 soil and water samples &lt;/span&gt;&lt;span style=&quot;font-size: 8.000000pt; font-family: 'ArialMT';&quot;&gt;and these were identified based on ITS and &lt;/span&gt;&lt;span style=&quot;font-size: 8.000000pt; font-family: 'Arial'; font-style: italic;&quot;&gt;cox&lt;/span&gt;&lt;span style=&quot;font-size: 8.000000pt; font-family: 'ArialMT';&quot;&gt;I sequence data. The 171 resulting &lt;/span&gt;&lt;span style=&quot;font-size: 8.000000pt; font-family: 'Arial'; font-style: italic;&quot;&gt;Phytophthora &lt;/span&gt;&lt;span style=&quot;font-size: 8.000000pt; font-family: 'ArialMT';&quot;&gt;isolates resided in 14 taxa including six known species (&lt;/span&gt;&lt;span style=&quot;font-size: 8.000000pt; font-family: 'Arial'; font-style: italic;&quot;&gt;P. multivora, P. capensis, P. cryptogea, P. frigida, P. cinnamomi, P. cinnamomi &lt;/span&gt;&lt;span style=&quot;font-size: 8.000000pt; font-family: 'ArialMT';&quot;&gt;var. &lt;/span&gt;&lt;span style=&quot;font-size: 8.000000pt; font-family: 'Arial'; font-style: italic;&quot;&gt;parvispora&lt;/span&gt;&lt;span style=&quot;font-size: 8.000000pt; font-family: 'ArialMT';&quot;&gt;), the known but as yet unnamed &lt;/span&gt;&lt;span style=&quot;font-size: 8.000000pt; font-family: 'Arial'; font-style: italic;&quot;&gt;Phytophthora &lt;/span&gt;&lt;span style=&quot;font-size: 8.000000pt; font-family: 'ArialMT';&quot;&gt;sp. PgChlamydo, &lt;/span&gt;&lt;span style=&quot;font-size: 8.000000pt; font-family: 'Arial'; font-style: italic;&quot;&gt;P. &lt;/span&gt;&lt;span style=&quot;font-size: 8.000000pt; font-family: 'ArialMT';&quot;&gt;sp. emzansi, and &lt;/span&gt;&lt;span style=&quot;font-size: 8.000000pt; font-family: 'Arial'; font-style: italic;&quot;&gt;P. &lt;/span&gt;&lt;span style=&quot;font-size: 8.000000pt; font-family: 'ArialMT';&quot;&gt;sp. Kununurra and &lt;/span&gt;&lt;span style=&quot;font-size: 8.000000pt; font-family: 'ArialMT';&quot;&gt;five novel taxa referred to as &lt;/span&gt;&lt;span style=&quot;font-size: 8.000000pt; font-family: 'Arial'; font-style: italic;&quot;&gt;P. &lt;/span&gt;&lt;span style=&quot;font-size: 8.000000pt; font-family: 'ArialMT';&quot;&gt;sp. stellaris, &lt;/span&gt;&lt;span style=&quot;font-size: 8.000000pt; font-family: 'Arial'; font-style: italic;&quot;&gt;P. &lt;/span&gt;&lt;span style=&quot;font-size: 8.000000pt; font-family: 'ArialMT';&quot;&gt;sp. Umtamvuna &lt;/span&gt;&lt;span style=&quot;font-size: 8.000000pt; font-family: 'Arial'; font-style: italic;&quot;&gt;P. &lt;/span&gt;&lt;span style=&quot;font-size: 8.000000pt; font-family: 'ArialMT';&quot;&gt;sp. canthium, &lt;/span&gt;&lt;span style=&quot;font-size: 8.000000pt; font-family: 'Arial'; font-style: italic;&quot;&gt;P. &lt;/span&gt;&lt;span style=&quot;font-size: 8.000000pt; font-family: 'ArialMT';&quot;&gt;sp. xWS, &lt;/span&gt;&lt;span style=&quot;font-size: 8.000000pt; font-family: 'Arial'; font-style: italic;&quot;&gt;P. &lt;/span&gt;&lt;span style=&quot;font-size: 8.000000pt; font-family: 'ArialMT';&quot;&gt;sp. xHennops. Four of the new taxa were found exclusively in water and two of these are hybrids. The most commonly isolated species from soil was &lt;/span&gt;&lt;span style=&quot;font-size: 8.000000pt; font-family: 'Arial'; font-style: italic;&quot;&gt;P. multivora&lt;/span&gt;&lt;span style=&quot;font-size: 8.000000pt; font-family: 'ArialMT';&quot;&gt;, a species recently described from Western Australia. &lt;/span&gt;&lt;span style=&quot;font-size: 8.000000pt; font-family: 'Arial'; font-style: italic;&quot;&gt;Phytophthora frigida &lt;/span&gt;&lt;span style=&quot;font-size: 8.000000pt; font-family: 'ArialMT';&quot;&gt;was isolated for the first time &lt;/span&gt;&lt;span style=&quot;font-size: 8.000000pt; font-family: 'ArialMT';&quot;&gt;from stream water. With the exception of &lt;/span&gt;&lt;span style=&quot;font-size: 8.000000pt; font-family: 'Arial'; font-style: italic;&quot;&gt;P. cinnamomi, &lt;/span&gt;&lt;span style=&quot;font-size: 8.000000pt; font-family: 'ArialMT';&quot;&gt;very little is known regarding the biology, epidemiology or origin of &lt;/span&gt;&lt;span style=&quot;font-size: 8.000000pt; font-family: 'Arial'; font-style: italic;&quot;&gt;Phytophthora &lt;/span&gt;&lt;span style=&quot;font-size: 8.000000pt; font-family: 'ArialMT';&quot;&gt;in South Africa. &lt;/span&gt;&lt;/p&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;</style></abstract><issue><style face="normal" font="default" size="100%">1</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%">Osterbauer, N. K.</style></author><author><style face="normal" font="default" size="100%">Griesbach, J. A.</style></author><author><style face="normal" font="default" size="100%">Hedberg, J.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Surveying for and eradicating Phytophthora ramorum in agricultural commodities</style></title><secondary-title><style face="normal" font="default" size="100%">Plant Health Progress</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2004</style></year></dates><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Since 2001, Oregon nurseries, Christmas tree plantations, and other sites have been surveyed for the federally regulated pathogen &lt;em&gt;Phytophthora ramorum&lt;/em&gt;. Host plants at each site were visually surveyed for disease symptoms and symptomatic tissues tested in the laboratory by isolation onto a selective medium and by a polymerase chain reaction (PCR) assay. In 2002 and 2003, we detected PCR-positive plants that later proved to be infected with another &lt;em&gt;Phytophthora&lt;/em&gt;, suggesting there are limitations to the PCR assay tested. In 2003, &lt;em&gt;P. ramorum&lt;/em&gt; was detected for the first time in &lt;em&gt;Viburnum, Pieris, Rhododendron&lt;/em&gt;, and &lt;em&gt;Camellia&lt;/em&gt; plants in six nurseries. All infected and neighboring plant materials were destroyed by incineration and the nurseries and surrounding environs subsequently surveyed for the pathogen. &lt;em&gt;Phytophthora ramorum&lt;/em&gt; was not detected, indicating the pathogen was successfully eradicated.&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%">Oßwald, W.</style></author><author><style face="normal" font="default" size="100%">Fleischmann, F.</style></author><author><style face="normal" font="default" size="100%">Rigling, D.</style></author><author><style face="normal" font="default" size="100%">Coelho, A. C.</style></author><author><style face="normal" font="default" size="100%">Cravador, A.</style></author><author><style face="normal" font="default" size="100%">Diez, J.</style></author><author><style face="normal" font="default" size="100%">Dalio, R. J.</style></author><author><style face="normal" font="default" size="100%">Horta Jung, M.</style></author><author><style face="normal" font="default" size="100%">Pfanz, H.</style></author><author><style face="normal" font="default" size="100%">Robin, C.</style></author><author><style face="normal" font="default" size="100%">Sipos, G.</style></author><author><style face="normal" font="default" size="100%">Solla, A.</style></author><author><style face="normal" font="default" size="100%">Cech, T.</style></author><author><style face="normal" font="default" size="100%">Chambery, A.</style></author><author><style face="normal" font="default" size="100%">Diamandis, S.</style></author><author><style face="normal" font="default" size="100%">Hansen, E.</style></author><author><style face="normal" font="default" size="100%">Jung, T.</style></author><author><style face="normal" font="default" size="100%">Orlikowski, L. B.</style></author><author><style face="normal" font="default" size="100%">Parke, J.</style></author><author><style face="normal" font="default" size="100%">Prospero, S.</style></author><author><style face="normal" font="default" size="100%">Werres, S.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Strategies of attack and defence in woody plant- Phytophthora interactions</style></title><secondary-title><style face="normal" font="default" size="100%">Forest Pathology</style></secondary-title><short-title><style face="normal" font="default" size="100%">For. Path.</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%">June 2014</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://doi.wiley.com/10.1111/efp.12096</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">44</style></volume><pages><style face="normal" font="default" size="100%">169–190</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 review comprises both well-known and recently described &lt;em&gt;Phytophthora&lt;/em&gt; species and concentrates on &lt;em&gt;Phytophthora&lt;/em&gt;–woody plant interactions. First, comprehensive data on infection strategies are presented which were the basis for three models that explain invasion and spread of &lt;em&gt;Phytophthora&lt;/em&gt; pathogens in different woody host plants. The first model describes infection of roots, the second concentrates on invasion of the trunk, and the last one summarizes infection and invasion of host plants via leaves. On the basis of morphological, physiological, biochemical and molecular data, scenarios are suggested which explain the sequences of reactions that occur in susceptible and tolerant plants following infections of roots or of stem bark. Particular emphasis is paid to the significance of &lt;em&gt;Phytophthora&lt;/em&gt; elicitins for such host–pathogen interactions. The overall goal is to shed light on the sequences of pathogenesis to better understand how &lt;em&gt;Phytophthora&lt;/em&gt; pathogens harm their host plants.&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%">W. Oßwald</style></author><author><style face="normal" font="default" size="100%">T. Jung</style></author><author><style face="normal" font="default" size="100%">Nechwatal, J.</style></author><author><style face="normal" font="default" size="100%">Schlenzig, A.</style></author><author><style face="normal" font="default" size="100%">F. Fleischmann</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Significance of Phytophthoras and Pythium for oak, alder and spruce decline.</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Forest Science</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2001</style></year></dates><volume><style face="normal" font="default" size="100%">47</style></volume><pages><style face="normal" font="default" size="100%">96-103 </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 results of a survey of soil borne Phytophthoras in 35 oak (&lt;em&gt;Quercus&lt;/em&gt;) stands on geologically different sites in Bavaria clearly showed that the most widespread species were identified as &lt;em&gt;Phytophthora citricola&lt;/em&gt;, &lt;em&gt;P. cambivora&lt;/em&gt; and &lt;em&gt;P. quercina&lt;/em&gt;. These three species were only isolated from rhizosphere soil of stands with mean soil pH-values (CaCl&lt;sub&gt;2&lt;/sub&gt;) of 3.5 and higher on loamy, clayey or sandy-loamy soil texture. At these &lt;em&gt;Phytophthora&lt;/em&gt; stands, all root parameters of declining oaks were significantly reduced as compared to healthy looking trees. It is concluded that the above mentioned &lt;em&gt;Phytophthora&lt;/em&gt; species are involved in oak decline as primary root rot pathogens on clay or sandy-loamy stands with soil pH-values higher than 3.5. A new &lt;em&gt;Phytophthora&lt;/em&gt; hybrid, called 'alder &lt;em&gt;Phytophthora&lt;/em&gt;', was isolated frequently from bark sections of declining alders along several Bavarian rivers and from nursery plants. PCR-RFLP analysis proved that the Bavarian isolates belonged to the same hybrid variants found in Great Britain, Sweden, France or Denmark. Spruce decline was studied in the Bavarian Alps on stands representing various site conditions. Most root parameters were negatively correlated with crown transparency. In addition, the total number of lateral roots was significantly lower for declining compared to healthy trees. Remarkably, only &lt;em&gt;Pythium&lt;/em&gt; species were isolated from rhizosphere soil, which were divided into several groups after PCR-RFLP analysis. In soil infestation tests, most of the isolates caused severe root damage on spruce similar to root rot seen on declining trees in the field.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">Special Issue</style></issue><work-type><style face="normal" font="default" size="100%">Journal article; Conference paper</style></work-type></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>10</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Parke, J. L.</style></author><author><style face="normal" font="default" size="100%">N. J. Grünwald</style></author><author><style face="normal" font="default" size="100%">C. Lewis</style></author><author><style face="normal" font="default" size="100%">V. Fieland</style></author></authors><secondary-authors><author><style face="normal" font="default" size="100%">Frankel, S.J.</style></author><author><style face="normal" font="default" size="100%">J.T. Kliejunas</style></author><author><style face="normal" font="default" size="100%">K. M. Palmieri</style></author></secondary-authors></contributors><titles><title><style face="normal" font="default" size="100%">A systems approach for detecting sources of Phytophthora contamination in nurseries</style></title><secondary-title><style face="normal" font="default" size="100%">Sudden oak death fourth science symposium</style></secondary-title></titles><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://www.fs.fed.us/psw/publications/documents/psw_gtr229/</style></url></web-urls></urls><pub-location><style face="normal" font="default" size="100%">Santa Cruz, California</style></pub-location><volume><style face="normal" font="default" size="100%">Gen. Tech. Rep. PSW-GTR-229</style></volume><pages><style face="normal" font="default" size="100%">67-68</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%">Parke, J. L.</style></author><author><style face="normal" font="default" size="100%">Lucas, S.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Sudden oak death and ramorum blight.</style></title><secondary-title><style face="normal" font="default" size="100%">The Plant Health Instructor</style></secondary-title></titles><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://www.apsnet.org/edcenter/intropp/lessons/fungi/Oomycetes/Pages/SuddenOakDeath.aspx</style></url></web-urls></urls><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>12</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Peterson, Ebba K</style></author><author><style face="normal" font="default" size="100%">Parke, Jennifer L.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Sudden oak death, sudden larch death, and ramorum blight​ </style></title><secondary-title><style face="normal" font="default" size="100%">American Phytopathological Society: The Plant Health Instructor</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2019</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://www.apsnet.org/edcenter/disandpath/oomycete/pdlessons/Pages/SuddenOakDeath.aspx</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">The American Phytopathological Society</style></publisher><pub-location><style face="normal" font="default" size="100%">St. Paul, MN</style></pub-location><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;&lt;span id=&quot;DeltaPlaceHolderMain&quot;&gt;&lt;em&gt;Phytophthora ramorum&lt;/em&gt; is a recently emerged pathogen with a host range of more than 150 plant species. This fungus-like organism causes sudden oak death on certain members of the oak family and has killed an estimated 30-45 million trees in coastal forests of California and Oregon. The pathogen additionally causes sudden larch death of Japanese larch, especially in conifer plantations in the United Kingdom. On most hosts, however, &lt;em&gt;P. ramorum&lt;/em&gt; causes ramorum leaf blight or shoot blight on native plant species and horticultural nursery crops, plaguing some nurseries in California, Oregon, Washington, British Columbia and Europe.&amp;nbsp; &lt;/span&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%">Peterson, Ebba</style></author><author><style face="normal" font="default" size="100%">Hansen, Everett</style></author><author><style face="normal" font="default" size="100%">Hulbert, Joseph</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Source or sink? The role of soil and water borne inoculum in the dispersal of Phytophthora ramorum in Oregon tanoak forests</style></title><secondary-title><style face="normal" font="default" size="100%">Forest Ecology and Management</style></secondary-title><short-title><style face="normal" font="default" size="100%">Forest Ecology and Management</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-06-2014</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://linkinghub.elsevier.com/retrieve/pii/S0378112714001261</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">322</style></volume><pages><style face="normal" font="default" size="100%">48 - 57</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Management of invasive species requires confidence in the detection methods used to assess expanding distributions, as well as an understanding of the dominant modes of spread. Lacking this basic biological information, during early stages of invasion management choices are often driven by available resources and the biology of closely related species. Such has been the case for the management of the phytopathogen, &lt;em&gt;Phytophthora ramorum&lt;/em&gt;, causal agent of sudden oak death (SOD) of oaks and tanoaks. To detect &lt;em&gt;P. ramorum&lt;/em&gt;, The Oregon SOD eradication program has relied upon the aerial observation of dead, overstory tanoak (&lt;em&gt;Notholithocarpus densiflorus&lt;/em&gt;), an easily infected host widely distributed throughout the range of &lt;em&gt;P. ramorum&lt;/em&gt; in Oregon. At risk is the possibility of misrepresenting the distribution of SOD, particularly if inoculum is predominately moved in soil and water, common dispersal pathways for other &lt;em&gt;Phytophthora&lt;/em&gt; spp. To assess this risk, we performed surveys of understory vegetation in areas with a high risk of establishment of understory infection from soil and water sources: along roadsides within heavily trafficked areas with a history of SOD, and along streams known to contain &lt;em&gt;P. ramorum&lt;/em&gt; inoculum. Additionally, we tested the alternative hypothesis of aerial dispersal, whereby infection in the understory would be spatially correlated with overstory mortality. Consistent with prior studies into the spatial structure of &lt;em&gt;P. ramorum&lt;/em&gt; in Oregon, we found no evidence of understory infection in close proximity to roads in the absence of overstory mortality. Similarly, &lt;em&gt;P. ramorum&lt;/em&gt; was only isolated from understory vegetation associated with streams when within close proximity to overstory sources, and more commonly further away from stream edges than within the splash and flood line. Both disease patterns are inconsistent with a dominate soil and water mediated dispersal mechanism. Rather, we found evidence supporting our alternative hypothesis of aerial dispersal whereby recovery of &lt;em&gt;P. ramorum&lt;/em&gt; in the understory declined with increasing distance from the only known overstory source. These results support the use of aerial detection in describing the distribution of SOD in Oregon, and give further support to dispersal of inoculum in blowing fog or rain at scales not yet described for other forest &lt;em&gt;Phytophthora&lt;/em&gt; species.&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%">Puértolas, Alexandra</style></author><author><style face="normal" font="default" size="100%">Boa, Eric</style></author><author><style face="normal" font="default" size="100%">Bonants, Peter J. M.</style></author><author><style face="normal" font="default" size="100%">Woodward, Steve</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Survival of Phytophthora cinnamomi and Fusarium verticillioides in commercial potting substrates for ornamental plants</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%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">Jan-08-2018</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://onlinelibrary.wiley.com/doi/abs/10.1111/jph.12708?campaign=woletoc</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">166</style></volume><pages><style face="normal" font="default" size="100%">484 - 493</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Live plants, particularly when accompanied by soil or potting substrates, are considered the main pathway for international spread of plant pathogens. Modern, rapid shipping technologies for international plant trade increase the probability of plant pathogen survival during transport and the subsequent chances of disease outbreaks in new locations. The survival of two model pathogens, an Oomycete, &lt;em&gt;Phytophthora cinnamomi&lt;/em&gt;, and a filamentous fungus, &lt;em&gt;Fusarium verticillioides&lt;/em&gt;, was studied in two different commercial potting substrates (peat and peat‐free) under glasshouse conditions in the absence of a plant host. Survival rates were analysed at 2, 7, 12 and 17&amp;nbsp;months after substrate inoculation. &lt;em&gt;Fusarium verticillioides&lt;/em&gt; had the longest survival rate, and was still present at 17&amp;nbsp;months. In contrast, &lt;em&gt;P.&amp;nbsp;cinnamomi&lt;/em&gt; survived up to 7&amp;nbsp;months but was not recovered after 12 or 17&amp;nbsp;months. There was no significant difference in the number of colony‐forming units (CFUs) of either pathogen in the two substrates, except at 2&amp;nbsp;months, when higher numbers were recovered from peat substrates.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">7-8</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%">Ríos, P.</style></author><author><style face="normal" font="default" size="100%">Obregón, S.</style></author><author><style face="normal" font="default" size="100%">González, M.</style></author><author><style face="normal" font="default" size="100%">de Haro, A.</style></author><author><style face="normal" font="default" size="100%">Sanchez, M. E.</style></author></authors><secondary-authors><author><style face="normal" font="default" size="100%">Woodward, S.</style></author></secondary-authors></contributors><titles><title><style face="normal" font="default" size="100%">Screening brassicaceous plants as biofumigants for management of Phytophthora cinnamomi oak disease</style></title><secondary-title><style face="normal" font="default" size="100%">Forest Pathology</style></secondary-title><short-title><style face="normal" font="default" size="100%">For. Path.</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-06-2016</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://doi.wiley.com/10.1111/efp.12287http://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fefp.12287</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;Brassicaceous plants rich in glucosinolates have been used as biofumigants for the management of soilborne pathogens. Efficacy of &lt;em&gt;Brassica&lt;/em&gt; plant tissue has mainly been attributed to toxic isothiocyanates released upon the hydrolysis of glucosinolates. Management of &lt;em&gt;Phytophthora cinnamomi&lt;/em&gt;, the causal agent of oak root rot in rangeland ecosystems using biofumigation, is promising, but requires further validation. The biofumigation activity of 14 brassicaceous plants was evaluated under experimental conditions. All evaluated plants rich in sinigrin suppressed (100%) the mycelial growth of &lt;em&gt;P.&amp;nbsp;cinnamomi&lt;/em&gt;, while plants rich in aromatic or other aliphatic glucosinolates had little or no suppressive effect. Simulating soil amendment in field conditions, the effects on natural soil artificially infested with &lt;em&gt;P.&amp;nbsp;cinnamomi&lt;/em&gt; chlamydospores were examined with &lt;em&gt;Brassica juncea&lt;/em&gt;,&lt;em&gt; Eruca vesicaria&lt;/em&gt; and &lt;em&gt;Lepidium sativum&lt;/em&gt;, three species with different glucosinolate profiles. Only &lt;em&gt;B.&amp;nbsp;juncea&lt;/em&gt; decreased the viability of chlamydospores significantly in comparison with untreated soil only 1&amp;nbsp;day after biofumigation, whereas &lt;em&gt;E&lt;/em&gt;. &lt;em&gt;vesicaria&lt;/em&gt; needed 8&amp;nbsp;days to reach significance and &lt;em&gt;L.&amp;nbsp;sativum&lt;/em&gt; had no effect at all. Despite the decreases in soil inoculum, biofumigation with &lt;em&gt;B.&amp;nbsp;juncea&lt;/em&gt; did not prevent the root infections in a highly susceptible host (&lt;em&gt;Lupinus luteus&lt;/em&gt;). However, biofumigation with plants rich in sinigrin, such as &lt;em&gt;B.&amp;nbsp;juncea&lt;/em&gt;, decreased &lt;em&gt;P.&amp;nbsp;cinnamomi&lt;/em&gt; soil inoculum under the experimental minimum threshold for oak disease expression. Although biofumigation should be considered as an effective measure to be incorporated in integrated control of the oak disease, biofumigation by itself would not be effective enough for the substantial suppression of &lt;em&gt;P.&amp;nbsp;cinnamomi&lt;/em&gt; inoculum.&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%">Robin, Cécile</style></author><author><style face="normal" font="default" size="100%">Desprez-Loustau, Marie-Laure</style></author><author><style face="normal" font="default" size="100%">Delatour, Claude</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Spatial and temporal enlargement of trunk cankers of Phytophthora cinnamomi in red oak</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%">1992</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://www.nrcresearchpress.com/doi/abs/10.1139/x92-047</style></url></web-urls></urls><number><style face="normal" font="default" size="100%">3</style></number><volume><style face="normal" font="default" size="100%">22</style></volume><pages><style face="normal" font="default" size="100%">362-366</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 cinnamomi&lt;/em&gt; Rands is the agent of ink disease on northern red oak (&lt;em&gt;Quercus rubra&lt;/em&gt; L.). Cortical cankers on the trunk are the visible symptoms. The fungus causes necrosis of the cambium and phloem, and the tree reacts by forming xylem callus curls. These features can be dated aposteriori on cross sections. The aim of this study was to describe the spatial and temporal development of cankers on cross-sectioned infected oaks. For each lesion, dates of cambium necrosis and formation of callus were recorded at different heights. The following parameters were measured for each lesion: age, height, rate of development, and length and duration of necrosis and canker. Two hundred sixty-three lesions, on 14 trees, were studied. Trees did not exhibit cankers before 9 years of age. All visible trunk cankers could be related to a collar lesion. &lt;em&gt;Phytophthora cinnamomi&lt;/em&gt; spreads upwards and can persist for several years, being active seasonally. In this study cambium necrosis occurred preferentially during the first flush. Twenty-nine percent of the lesions were healed over at the collar after 1 year. The collar was less susceptible than the trunk. The other lesions spread rapidly in the cambium of the trunk, which was very vulnerable. They then progressively healed. Therefore, the canker progress curve was bell shaped.&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%">Rodríguez-Molina, M. C.</style></author><author><style face="normal" font="default" size="100%">Blanco-Santos, A.</style></author><author><style face="normal" font="default" size="100%">Palo-Núñez, E. J.</style></author><author><style face="normal" font="default" size="100%">Torres-Vila, L. M.</style></author><author><style face="normal" font="default" size="100%">Torres-Álvarez, E.</style></author><author><style face="normal" font="default" size="100%">Suárez-de-la-Cámara, M. A.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Seasonal and spatial mortality patterns of holm oak seedlings in a reforested soil infected with Phytophthora cinnamomi</style></title><secondary-title><style face="normal" font="default" size="100%">Forest Pathology</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2005</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1111/j.1439-0329.2005.00423.x</style></url></web-urls></urls><number><style face="normal" font="default" size="100%">6</style></number><publisher><style face="normal" font="default" size="100%">Blackwell Verlag GmbH</style></publisher><volume><style face="normal" font="default" size="100%">35</style></volume><pages><style face="normal" font="default" size="100%">411–422</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Summary The viability of 1-year-old holm oak (&lt;em&gt;Quercus ilex&lt;/em&gt;) seedlings in a soil naturally infected with &lt;em&gt;Phytophthora cinnamomi&lt;/em&gt; was studied during 2 consecutive years in a plot located in south-western Spain. In both years, total mortality during autumn and winter was not noticeable (&amp;lt;2.1%). In spring, mortality levels were higher (8.3–4.6%), especially the first year. A steep increase in total mortality occurred in summer, both in the first (11.4%) and second (24.2%) year, but mortality attributable to &lt;em&gt;P. cinnamomi&lt;/em&gt; was 1.9 and 7.6%, respectively. Thus, 2 years after planting, total cumulative mortality was 43.4%, and that attributable to &lt;em&gt;P. cinnamomi&lt;/em&gt; 9.6% (i.e. 22.1% of total mortality). Fungus-derived mortality followed a spatially aggregated pattern in the reforestation plot, suggesting a clustered distribution of the inoculum in the soil. Furthermore, mortality by &lt;em&gt;P. cinnamomi&lt;/em&gt; was also associated with nearness of infected adult trees in the plot. Results obtained are discussed in the framework of seasonal water deficit, &lt;em&gt;P. cinnamomi&lt;/em&gt; damage, weed competition and sanitation techniques to be used in declined holm oak stands in Spain.&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%">Rosenbaum, J.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Studies of the genus Phytophthora</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Agricultural Research </style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">1917</style></year></dates><volume><style face="normal" font="default" size="100%">8</style></volume><pages><style face="normal" font="default" size="100%">233-276</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><issue><style face="normal" font="default" size="100%">7</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%">Rosenthal, Lisa Micaela</style></author><author><style face="normal" font="default" size="100%">Fajardo, Sebastian N.</style></author><author><style face="normal" font="default" size="100%">Rizzo, David</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Sporulation potential of Phytophthora ramorum differs among common California plant species in the Big Sur region</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%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">Nov-17-2020</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://apsjournals.apsnet.org/doi/10.1094/PDIS-03-20-0485-RE</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;Sudden oak death (SOD), caused by the generalist pathogen &lt;em&gt;Phytophthora ramorum&lt;/em&gt;, has profoundly impacted California coastal ecosystems. SOD has largely been treated as a two-host system, with &lt;em&gt;Umbellularia californica&lt;/em&gt; as the most transmissive host, &lt;em&gt;Notholithocarpus densiflorus&lt;/em&gt; less so, and remaining species as epidemiologically unimportant. However, this understanding of transmission potential primarily stems from observational field studies rather than direct measurements on the diverse assemblage of plant species. Here, we formally quantify the sporulation potential of common plant species inhabiting SOD-endemic ecosystems on the California coast in the Big Sur region. This study allows us to better understand the pathogen’s basic biology, trajectory of SOD in a changing environment, and how the entire host community contributes to disease risk. Leaves were inoculated in a controlled laboratory environment and assessed for production of sporangia and chlamydospores, the infectious and resistant propagules, respectively. &lt;em&gt;P. ramorum&lt;/em&gt; was capable of infecting every species in our study and almost all species produced spores to some extent. Sporangia production was greatest in &lt;em&gt;N. densiflorus&lt;/em&gt; and &lt;em&gt;U. californica&lt;/em&gt; and the difference was insignificant. Even though other species produced much less, quantities were non-zero. Thus, additional species may play a previously unrecognized role in local transmission. Chlamydospore production was highest in &lt;em&gt;Acer macrophyllum&lt;/em&gt; and &lt;em&gt;Ceanothus oliganthus&lt;/em&gt;, raising questions about the role they play in pathogen persistence. Lesion size did not consistently correlate with the production of either sporangia or chlamydospores. Overall, we achieved an empirical foundation to better understand how community composition affects transmission of &lt;em&gt;P. ramorum&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%">Rosso, P. H.</style></author><author><style face="normal" font="default" size="100%">Baccalá,  N</style></author><author><style face="normal" font="default" size="100%">Havrylenko, M</style></author><author><style face="normal" font="default" size="100%">Fontenla, S</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Spatial pattern of Austrocedrus chilensis wilting and the scope of autocorrelation analysis in natural forests</style></title><secondary-title><style face="normal" font="default" size="100%">Forest Ecology and Management</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">1994</style></year><pub-dates><date><style  face="normal" font="default" size="100%">AUG 1994</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org.proxy.library.oregonstate.edu/10.1016/0378-1127(94)90022-1</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">67</style></volume><pages><style face="normal" font="default" size="100%">273-279</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%">Roux, Jolanda</style></author><author><style face="normal" font="default" size="100%">Wingfield, Michael J.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Survey and virulence of fungi occurring on diseased Acacia mearnsii in South Africa</style></title><secondary-title><style face="normal" font="default" size="100%">Forest Ecology and Management</style></secondary-title><short-title><style face="normal" font="default" size="100%">Forest Ecology and Management</style></short-title></titles><dates><year><style  face="normal" font="default" size="100%">1997</style></year><pub-dates><date><style  face="normal" font="default" size="100%">Jan-12-1997</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1016/s0378-1127(97)00110-2 </style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">99</style></volume><pages><style face="normal" font="default" size="100%">327 - 336</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Various disease symptoms occur on &lt;em&gt;Acacia mearnsii&lt;/em&gt; in South Africa, of which black butt, on older trees, is the most common. Other less commonly reported symptoms include gummosis, cracks, discoloured lesions and die-back. These diseases are of unknown aetiology. During a 2-year period, a survey of diseases on &lt;em&gt;A. mearnsii&lt;/em&gt; was conducted in two major commercial wattle-growing areas of South Africa. Samples were collected from all symptomatic tissue on randomly selected trees in each area. A wide range of fungi were isolated, including species of &lt;em&gt;Phytophthora, Seiridium, Sphaeropsis, Fusarium, Diplodia, Ceratocystis&lt;/em&gt; and &lt;em&gt;Botryosphaeria&lt;/em&gt;. Of these, &lt;em&gt;Phytophthora&lt;/em&gt; spp. were isolated only from basal lesions and soil, whereas the &lt;em&gt;Diplodia&lt;/em&gt; and &lt;em&gt;Fusarium&lt;/em&gt; spp. were the most frequently isolated from diseased tissue on aboveground parts of trees. &lt;em&gt;Phytophthora parasitica&lt;/em&gt; and &lt;em&gt;Ceratocystis albofundus&lt;/em&gt;, which are well-known pathogens of &lt;em&gt;A. mearnsii&lt;/em&gt;, were excluded from the pathogenicity tests. All other fungi isolated, and particularly those belonging to genera that are known plant pathogens, were used in pathogenicity tests to determine their possible role in diseases. For each isolate, 20 saplings were inoculated in the field, and the resultant lesion lengths were measured. Only the &lt;em&gt;Phytophthora&lt;/em&gt; spp., &lt;em&gt;Botryosphaeria&lt;/em&gt; sp. and &lt;em&gt;Sphaeropsis&lt;/em&gt; sp. produced noticeable lesions. From the surveys and pathogenicity tests, it is clear that many fungi are associated with diseases of &lt;em&gt;A. mearnsii&lt;/em&gt;, and that these deserve further study.&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%">Santini, Alberto</style></author><author><style face="normal" font="default" size="100%">Barzanti, Gian Paolo</style></author><author><style face="normal" font="default" size="100%">Capretti, Paolo</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Susceptibility of some mesophilic hardwoods to alder Phytophthora</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%">Alnus cordata</style></keyword><keyword><style  face="normal" font="default" size="100%">Alnus glutinosa</style></keyword><keyword><style  face="normal" font="default" size="100%">Castanea sativa</style></keyword><keyword><style  face="normal" font="default" size="100%">Hardwoods</style></keyword><keyword><style  face="normal" font="default" size="100%">inoculation test</style></keyword><keyword><style  face="normal" font="default" size="100%">Juglans regia</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytophthora cinnamomi</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytophthora spp.</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus robur</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2003</style></year><pub-dates><date><style  face="normal" font="default" size="100%">08/2003</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1046/j.1439-0434.2003.00739.x</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">151</style></volume><pages><style face="normal" font="default" size="100%">406–410</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Abstract Inoculation tests were carried out in the greenhouse on seedlings of five hardwoods (&lt;em&gt;Alnus cordata, A. glutinosa, Castanea sativa, Juglans regia&lt;/em&gt; and &lt;em&gt;Quercus robur&lt;/em&gt;) to determine their susceptibility to an isolate of alder &lt;em&gt;Phytophthora&lt;/em&gt; obtained in Italy from &lt;em&gt;A. cordata. A Phytophthora cinnamomi&lt;/em&gt; strain was used for comparison. Host susceptibility to infection was determined as the lesion length after stem inoculation and the percentage of necrotized rootlets after soil infestation with inoculated millet seeds. The aggressiveness of the alder &lt;em&gt;Phytophthora&lt;/em&gt; isolate was significantly higher in the two &lt;em&gt;Alnus&lt;/em&gt; species than in the other hosts. Our results were confirmed with both methods of inoculation. &lt;em&gt;Alnus cordata&lt;/em&gt; was consistently the most susceptible host species when compared with the other hardwoods. Damage by &lt;em&gt;P. cinnamomi&lt;/em&gt; was severe, particularly after soil infestation tests. The most susceptible species were alders, chestnut and walnut. The test also suggests that alder &lt;em&gt;Phytophthora&lt;/em&gt; is able to spread through infected seedlings of different hardwood species.&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%">Serrano, M. S.</style></author><author><style face="normal" font="default" size="100%">De Vita, P.</style></author><author><style face="normal" font="default" size="100%">Carbonero, M. D.</style></author><author><style face="normal" font="default" size="100%">Fernández, F.</style></author><author><style face="normal" font="default" size="100%">Fernández-Rebollo, P.</style></author><author><style face="normal" font="default" size="100%">Sánchez, M. E.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Susceptibility to Phytophthora cinnamomi of the commonest morphotypes of Holm oak in southern Spain</style></title><secondary-title><style face="normal" font="default" size="100%">Forest Pathology</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://dx.doi.org/10.1111/j.1439-0329.2011.00758.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%">42</style></volume><pages><style face="normal" font="default" size="100%">345–347</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 four main morphotypes of Holm oak (&lt;em&gt;Quercus ilex&lt;/em&gt; subsp. &lt;em&gt;ballota&lt;/em&gt;) present in Andalusia (&lt;em&gt;expansa&lt;/em&gt;, &lt;em&gt;macrocarpa&lt;/em&gt;, &lt;em&gt;microcarpa&lt;/em&gt; and &lt;em&gt;rotundifolia&lt;/em&gt;) were infected with &lt;em&gt;Phytophthora cinnamomi&lt;/em&gt; to determine their susceptibility to the root pathogen. No large differences were found among the four morphotypes in the infection of roots, which always showed a high degree of necrosis. However, the different responses of the foliage to infection separated the four morphotypes of Holm oak into three groups: very susceptible (&lt;em&gt;microcarpa&lt;/em&gt;), susceptible (&lt;em&gt;expansa&lt;/em&gt;) and moderately susceptible (&lt;em&gt;rotundifolia&lt;/em&gt; and &lt;em&gt;macrocarpa&lt;/em&gt;). The natural hybrid &lt;em&gt;Q.ilex ballota&lt;/em&gt;-&lt;em&gt;Q.faginea&lt;/em&gt; exhibited a low level of root and foliar symptoms when infected with &lt;em&gt;P.cinnamomi&lt;/em&gt;. &lt;em&gt;Quercus faginea&lt;/em&gt; could be considered as a source of resistance to &lt;em&gt;P.cinnamomi&lt;/em&gt; in future breeding programmes.&lt;/p&gt;</style></abstract></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>10</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Dr. Patrick J. Shea</style></author><author><style face="normal" font="default" size="100%">Dr. Richard B. Standiford</style></author><author><style face="normal" font="default" size="100%">Dr. Patrick J. Shea</style></author><author><style face="normal" font="default" size="100%">Dr. Richard B. Standiford</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Sudden oak death, a science symposium: the state of our knowledge (abstracts)</style></title><secondary-title><style face="normal" font="default" size="100%">Sudden oak death, a science symposium - the state of our knowledge</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2002</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2002</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://www.suddenoakdeath.org/?bibliography=a-survey-of-sudden-oak-death-in-native-california-forest-and-woodland-communities-relating-incidence-and-intensity-of-phytophthora-ramorum-to-plant-community-and-site-variables</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">U.S. Department of Agriculture, Forest Service, Pacific Southwest Research Station, University of California, Integrated Hardwood and Range Management Program, Center for Forestry, Division of Agriculture and Natural Resources, Berkeley, California</style></publisher><pub-location><style face="normal" font="default" size="100%">Monterey, California</style></pub-location><pages><style face="normal" font="default" size="100%">98 pp</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Conference Purpose A Symposium designed to bring together a broad array of the scientific community from throughout the world working on &lt;em&gt;Phytophthora ramorum&lt;/em&gt; and the phenomena known as “Sudden Oak Death”&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%">Sims, Laura L.</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%">Susceptibility to the rare Phytophthora tentaculata and to the widespread Phytophthora cactorum is consistent with host ecology and history</style></title><secondary-title><style face="normal" font="default" size="100%">Forest Pathology</style></secondary-title><short-title><style face="normal" font="default" size="100%">For. Path.</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%">Apr-05-2020</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://onlinelibrary.wiley.com/doi/abs/10.1111/efp.12446?campaign=wolearlyview</style></url></web-urls></urls><pages><style face="normal" font="default" size="100%">e12446</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 evaluated the susceptibility of three California endemic plant species &lt;em&gt;Heteromeles arbutifolia&lt;/em&gt;,&lt;em&gt; Platanus racemosa&lt;/em&gt; and &lt;em&gt;Quercus agrifolia&lt;/em&gt; to the two congeneric soilborne pathogen species: &lt;em&gt;Phytophthora tentaculata&lt;/em&gt; and &lt;em&gt;Phytophthora cactorum&lt;/em&gt;. These pathogens were recently introduced in ecosystems east of the San Francisco Bay, where the three plant species above are dominant. &lt;em&gt;Phytophthora cactorum&lt;/em&gt; has a worldwide distribution inclusive of California, and a broad host range. &lt;em&gt;Phytophthora tentaculata&lt;/em&gt;, in contrast, is suspected to be a “new” exotic to California and has been described on relatively few hosts. By separately challenging the roots and the stems of the three plant species above, we show that: (a) Both were equally pathogenic, but the type of disease differed based on host; (b) disease was consistent with host ecology and with previous disease reports, even if caused by different &lt;em&gt;Phytophthora&lt;/em&gt; spp. and; (c) there were intraspecific differences in virulence. This study provides the following significant information regarding the management and early modelling of polyphagous soilborne &lt;em&gt;Phytophthoras&lt;/em&gt;: (a) Endemic species can be as problematic as recently introduced exotics. (b) Multiple introductions should be avoided due to varying virulence levels among genotypes. (c) Riparian species like &lt;em&gt;P.&amp;nbsp;racemosa&lt;/em&gt; may develop disease tolerance in their root systems, but remain susceptible in their aerial portions, and thus, diseases could be facilitated by flooding or splash of infectious structures of soilborne pathogens onto aerial plant portions.&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%">Sutton, W.</style></author><author><style face="normal" font="default" size="100%">Hansen, E.M.</style></author><author><style face="normal" font="default" size="100%">Reeser, Paul W.</style></author><author><style face="normal" font="default" size="100%">Kanaskie, Alan</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Stream monitoring for detection of Phytophthora ramorum in Oregon tanoak forests</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%">2009</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1094/PDIS-93-11-1182</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">93</style></volume><pages><style face="normal" font="default" size="100%">1182–1186</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Stream monitoring using leaf baits for early detection of &lt;em&gt;Phytophthora ramorum&lt;/em&gt; has been an important part of the Oregon Sudden Oak Death (SOD) program since 2002. Sixty-four streams in and near the Oregon quarantine area in the southwest corner of the state were monitored in 2008. Leaves of rhododendron (&lt;em&gt;Rhododendron macrophyllum&lt;/em&gt;) and tanoak (&lt;em&gt;Lithocarpus densiflorus&lt;/em&gt;) were placed in mesh bags, and bags were floated in streams. Leaf baits were exchanged every 2 weeks throughout the year. Leaves were assayed by isolation on selective medium and by multiplex rDNA internal transcribed spacer polymerase chain reaction (ITS PCR). The two methods gave comparable results, but multiplex PCR was more sensitive. &lt;em&gt;P. ramorum&lt;/em&gt; was regularly recovered at all seasons of the year from streams draining infested sites 5 years after eradication treatment. In streams with lower inoculum densities, recovery was much higher in summer than in winter. &lt;em&gt;P. ramorum&lt;/em&gt; was isolated from streams in 23 watersheds. When &lt;em&gt;P. ramorum&lt;/em&gt; was detected, intensive ground surveys located infected tanoaks or other host plants an average of 306 m upstream from the bait station. &lt;em&gt;P. ramorum&lt;/em&gt; was isolated from stream baits up to 1,091 m from the probable inoculum source.&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%">Edward J. Trione</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Sporulation and germination of Phytophthora lateralis</style></title><secondary-title><style face="normal" font="default" size="100%">Phytopathology</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">1974</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://www.apsnet.org/publications/phytopathology/backissues/Documents/1974Abstracts/Phyto64_1531.htm</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">64</style></volume><pages><style face="normal" font="default" size="100%">1531-1533</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%">Uchida, K.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Studies on the trunk rot of Japanese chestnut trees caused by Phytophthora castaneae</style></title><secondary-title><style face="normal" font="default" size="100%">Bulletin of the Ibaraki-ken Horticultural Experiment Station</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">1976</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://www.cabdirect.org/abstracts/19791352311.html</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">Special Issue 3</style></volume><pages><style face="normal" font="default" size="100%">48 pp.</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Since its discovery in 1962 this disease of &lt;em&gt;Castanea crenata&lt;/em&gt; has spread throughout the chestnut growing area and causes particularly severe damage in young orchards with bare ground between the trees. The fungus attacks trunks, branches, shoots and exposed roots, producing symptoms of black sap exudation from bark lesions which enlarge to girdle the trunk. A P. sp. isolated from lesion margins and described as &lt;em&gt;P. castaneae&lt;/em&gt; [RPP 57, 2024] was shown to be pathogenic to chestnut and oak, and to rot inoculated apple and Japanese pear fruits. The opt. temp. for mycelial growth was 27 deg and for oospore production 20-30 deg C. The pathogen survives as oospores in infested soil and was isolated using young chestnut shoots as bait. The population density of &lt;em&gt;P. castaneae&lt;/em&gt; in orchard soils was not correlated with disease severity. Every cv. of &lt;em&gt;C. crenata&lt;/em&gt; tested was susceptible and also the European chestnut (C. sativa), but Chinese chestnut (&lt;em&gt;C. mollissima&lt;/em&gt;) and American chestnut (&lt;em&gt;C. dentata&lt;/em&gt;) were resistant. The disease was controlled by grassing infested orchards and damage was reduced by grass mulches. Sprays of Difolatan [captafol] or Bordeaux on the trunks from early May to early June were effective, especially when combined with insecticide sprays. Fungicide applications to the soil or to the trunks after early June were ineffective.&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%">Vercauteren, A.</style></author><author><style face="normal" font="default" size="100%">Riedel, M.</style></author><author><style face="normal" font="default" size="100%">Maes, M.</style></author><author><style face="normal" font="default" size="100%">Werres, S.</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%">Survival of Phytophthora ramorum in Rhododendron root balls and in rootless substrates</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%">baiting</style></keyword><keyword><style  face="normal" font="default" size="100%">detection</style></keyword><keyword><style  face="normal" font="default" size="100%">latent survival</style></keyword><keyword><style  face="normal" font="default" size="100%">Sudden oak death</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.1365-3059.2012.02627.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%">62</style></volume><pages><style face="normal" font="default" size="100%">166–176</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 assesses the survival of &lt;em&gt;Phytophthora ramorum&lt;/em&gt; in the root ball of &lt;em&gt;Rhododendron&lt;/em&gt; container plants as well as in different rootless forest substrates and a horticultural potting medium. Following inoculation of the root balls, the aboveground plant parts stayed symptomless, whilst the pathogen could be recovered with a novel non-destructive baiting assay from the root balls until at least 8&amp;nbsp;months post-inoculation. Plating of surface-sterilized roots and direct microscopic analysis confirmed the presence of &lt;em&gt;P.&amp;nbsp;ramorum&lt;/em&gt; in the roots. &lt;em&gt;Phytophthora ramorum&lt;/em&gt; could also be baited from the root balls of symptomless &lt;em&gt;Rhododendron&lt;/em&gt; plants from commercial nurseries, even 2&amp;nbsp;years after acquisition. Survival of &lt;em&gt;P.&amp;nbsp;ramorum&lt;/em&gt; in rootless media was assessed after burying disks of infected leaf material below the soil surface in columns filled with four different undisturbed forest substrates or a potting medium, and incubated at an outdoor quarantine facility. &lt;em&gt;Phytophthora ramorum&lt;/em&gt; could be recovered at least 33&amp;nbsp;months after burial from all substrates, with a significant increase in recovery after the winter period. These data suggest the possibility for long-term symptomless presence of &lt;em&gt;P.&amp;nbsp;ramorum&lt;/em&gt; in root balls of commercial &lt;em&gt;Rhododendron&lt;/em&gt; plants as well as survival in potting medium and different forest substrates under western European climate conditions. Symptomless presence in root balls can contribute to latent spread of this pathogen between nurseries. The novel baiting test, being non-destructive, simple and applicable to a relatively large number of plants, can offer a valuable tool to test plants for the presence of &lt;em&gt;Phytophthora&lt;/em&gt; species in root balls.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">1</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%">A.M. Vettraino</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%">Scotch broom: a new host of Phytophthora megasperma in Italy</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%">2003</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1046/j.1365-3059.2003.00839.x</style></url></web-urls></urls><number><style face="normal" font="default" size="100%">3</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%">417–417</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%">Waipara, N.W.</style></author><author><style face="normal" font="default" size="100%">Hill, S.</style></author><author><style face="normal" font="default" size="100%">Hill, L.M.W.</style></author><author><style face="normal" font="default" size="100%">Hough, E.G.</style></author><author><style face="normal" font="default" size="100%">Horner, I.J.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Surveillance methods to determine tree health, distribution of kauri dieback disease and associated pathogens</style></title><secondary-title><style face="normal" font="default" size="100%">New Zealand Plant Protection</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2013</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://www.nzpps.org/nzpp_abstract.php?paper=662350</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">66</style></volume><pages><style face="normal" font="default" size="100%">235–241</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Kauri dieback is a pest issue that is increasingly affecting kauri forests. A water and soilborne pathogen, Phytophthora taxon Agathis (PTA), has been identified as a causal agent of kauri dieback at multiple locations, particularly within Auckland and Northland. In 2008, a passive surveillance and adaptive management programme was initiated to manage the disease across the natural range of kauri. Surveys were initially undertaken to determine the distribution and rate of spread of kauri dieback on private land in the Auckland region. Methods to evaluate and monitor overall tree health, disease symptoms and other potential contributing factors were developed. Diagnostic sampling was undertaken to isolate and identify pathogens associated with kauri dieback. Along with PTA, other Phytophthora species and environmental stress were frequently associated with symptoms at over 400 properties inspected. Further management is now required to develop control tools and mitigate further spread.&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%">Widmer, TL</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Survival of Phytophthora kernoviae oospores, sporangia, and mycelium</style></title><secondary-title><style face="normal" font="default" size="100%">New Zealand Journal of Forestry Science</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2011</style></year><pub-dates><date><style  face="normal" font="default" size="100%">07/2011</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://www.ars.usda.gov/research/publications/publications.htm?seq_no_115=259635</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">41S</style></volume><pages><style face="normal" font="default" size="100%">15-23</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Interpretive Summary: A recently discovered plant pathogen has been found to attack many different hosts including rhododendrons and beech trees in the United Kingdom and New Zealand. Although not currently known to exist in the United States, it is a pathogen of concern due to its destructive nature and threat to valuable hosts in the U.S. This pathogen produces different propagules for spread and survival of which very little is known. This study was done to learn how long these propagules can survive at different temperatures. Results show that one propagule type can survive buried in sand for up to a year at moderate temperatures but declines rapidly when exposed for increased periods of time as temperatures increase. In addition, this pathogen is able to persist and produce survival propagules in sand with very minimal nutrients. These results provide information to regulatory agency personnel and scientists to develop guidelines that help in limiting the spread of this pathogen. Technical Abstract: &lt;em&gt;Phytophthora kernoviae&lt;/em&gt; is a pathogen recently found only in the U.K. and New Zealand. &lt;em&gt;Phytophthora kernoviae&lt;/em&gt;, not known to produce chlamydospores, is homothallic and produces abundant oospores and sporangia. This study was conducted to examine long-term survival of oospores, sporangia, and mycelium buried in sand at different temperatures. Viability of oospores embedded onto 20-µm-mesh screens and buried in sand at 4, 10, 20, and 30C was measured over time by staining with tetrazolium bromide solution. For one isolate, viability was 82, 81, 79, and 58% and 86, 75, 82, and 78% for the other isolate at 4, 10, 20, and 30C, respectively, after 1 year. The infection potential of the oospores was checked by removing additional embedded screens and placing on rhododendron leaf disks. No necrosis was observed on leaf disks exposed to oospores buried for 1 year at 30C. However, necrosis was observed on leaf disks at the other temperatures after the same time. Oospores exposed 6 h at 50C and 24 h at 40 and 50C were less viable than controls and did not germinate. To study survival of sporangia and mycelium, sand was infested only with sporangia or mycelium from four isolates, incubated at different temperatures, and plated on &lt;em&gt;Phytophthora&lt;/em&gt;-selective medium over time. All isolates reacted in the same manner with populations generally declining within 1 week but then remaining steady over time. Soil extractions of the infested sand showed that over time sporangia and oospores formed at all temperatures except at 30C. This demonstrates that &lt;em&gt;P. kernoviae&lt;/em&gt; oospores can persist in sand for long periods of time at different temperatures, which could be a significant factor in spread of this pathogen.&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%">Zeng, Hui-cai</style></author><author><style face="normal" font="default" size="100%">Ho, Hon-hing</style></author><author><style face="normal" font="default" size="100%">Zheng, Fuy-Cong</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">A survey of Phytophthora species on Hainan Island of south China</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%">marine isolates</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytophthora capsici</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytophthora cinnamomi</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytophthora citrophthora</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytophthora heveae</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytophthora insolita</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytophthora katsurae</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytophthora nicotianae</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.1439-0434.2008.01441.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%">157</style></volume><pages><style face="normal" font="default" size="100%">33–39</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Abstract During the period 1997–2007, a comprehensive study of the occurrence and distribution of &lt;em&gt;Phytophthora&lt;/em&gt; species was conducted on Hainan Island of South China. To date, 14 species of &lt;em&gt;Phytophthora&lt;/em&gt; have been recovered and their distribution determined. &lt;em&gt;Phytophthora nicotianae (=P. parasitica)&lt;/em&gt; is the most important species attacking a wide variety of crops, followed by &lt;em&gt;Phytophthora capsici&lt;/em&gt; and &lt;em&gt;Phytophthora citrophthora&lt;/em&gt;. In contrast to &lt;em&gt;Phytophthora colocasiae&lt;/em&gt; attacking taro leaves throughout the entire island, &lt;em&gt;Phytophthora cyperi&lt;/em&gt; was found only once on &lt;em&gt;Digitaria ciliaris&lt;/em&gt; in Danzhou. It is of interest to note that &lt;em&gt;Phytophthora heveae, Phytophthora katsurae&lt;/em&gt; and &lt;em&gt;Phytophthora insolita&lt;/em&gt; are commonly found in forest soil/water of protected mountains without causing any plant diseases. Although &lt;em&gt;Phytophthora&lt;/em&gt; species are usually terrestrial or found in fresh water, one isolate of &lt;em&gt;Phytophthora&lt;/em&gt; resembling closely the asexual isolates of &lt;em&gt;P. insolita&lt;/em&gt; in Hainan was obtained from decaying &lt;em&gt;Rhizophora&lt;/em&gt; leaves submerged in seawater. An unidentified &lt;em&gt;Phytophthora&lt;/em&gt; species producing non-papillate; internally proliferating sporangia was isolated from the soil in which &lt;em&gt;Ceriops tagel&lt;/em&gt; and &lt;em&gt;Bruguiera serangula&lt;/em&gt; were growing in a salt water shrimp farm.&lt;/p&gt;</style></abstract></record></records></xml>