<?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%">Moralejo, E.</style></author><author><style face="normal" font="default" size="100%">Pérez-Sierra, A. M.</style></author><author><style face="normal" font="default" size="100%">Álvarez, L. A.</style></author><author><style face="normal" font="default" size="100%">Belbahri, L.</style></author><author><style face="normal" font="default" size="100%">Lefort, F.</style></author><author><style face="normal" font="default" size="100%">Descals, E.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Multiple alien Phytophthora taxa discovered on diseased ornamental plants in Spain</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%">2009</style></year><pub-dates><date><style  face="normal" font="default" size="100%">Jan-02-2009</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://doi.wiley.com/10.1111/j.1365-3059.2008.01930.x</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">58</style></volume><pages><style face="normal" font="default" size="100%">100 - 110</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 plant trade is unwittingly accelerating the worldwide spread of well‐known and new or undescribed &lt;em&gt;Phytophthora&lt;/em&gt; species and creating novel niches for emerging pathogens. The results of a survey carried out from 2001 to 2006 in garden centres and nurseries of the Balearic Islands and eastern Spain combined with the analysis of samples received from ornamental nurseries from northern Spain reflected the extent of this global issue at the local scale. A total of 125 &lt;em&gt;Phytophthora&lt;/em&gt; isolates were obtained from 37 different host species and 17 putative species identified on morphological features and direct sequencing of the internal transcribed spacer and four mitochondrial and nuclear genes. Five species, &lt;em&gt;P. ramorum&lt;/em&gt;, &lt;em&gt;P. hedraiandra&lt;/em&gt;, &lt;em&gt;P&lt;/em&gt;. ‘niederhauserii’, &lt;em&gt;P&lt;/em&gt;. ‘kelmania’ and &lt;em&gt;P&lt;/em&gt;. ‘taxon Pgchlamydo’ were formally unknown to science prior to 2001. In addition, 37 new host/pathogen combinations were first records for Spain, highlighting the risk of non‐coevolved organisms from different biogeographic origins coming into contact under managed environments. The problem generated by new or rare taxa of &lt;em&gt;Phytophthora&lt;/em&gt; found in nurseries for which no prior information on natural habitat and ecology is available for pest risk analysis is discussed.&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%">Moralejo, E.</style></author><author><style face="normal" font="default" size="100%">Puig, M.</style></author><author><style face="normal" font="default" size="100%">Man in't Veld, W. A.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">First report of Phytophthora tentaculata on Verbena sp. in Spain</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 Pathology</style></short-title></titles><dates><year><style  face="normal" font="default" size="100%">2004</style></year><pub-dates><date><style  face="normal" font="default" size="100%">Jan-12-2004</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://www.blackwell-synergy.com/toc/ppa/53/6http://doi.wiley.com/10.1111/j.1365-3059.2004.01089.xhttp://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fj.1365-3059.2004.01089.x</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">53</style></volume><pages><style face="normal" font="default" size="100%">806 - 806</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;div id=&quot;ss3&quot; class=&quot;section&quot;&gt;&lt;div class=&quot;para&quot;&gt;&lt;p&gt;The oomycete &lt;em&gt;Phytophthora tentaculata&lt;/em&gt; causes root and stalk rot of &lt;em&gt;Chrysanthemum&lt;/em&gt; spp., &lt;em&gt;Delphinium ajacis&lt;/em&gt; and &lt;em&gt;Verbena&lt;/em&gt; spp. in nurseries in the Netherlands and Germany (&lt;a class=&quot;referenceLink&quot; title=&quot;Link to bibliographic citation&quot; href=&quot;http://onlinelibrary.wiley.com.ezproxy.proxy.library.oregonstate.edu/doi/10.1111/j.1365-3059.2004.01089.x/full#b1&quot; rel=&quot;references:#b1&quot;&gt;Kröber &amp;amp; Marwitz, 1993&lt;/a&gt;). In June 2001, &lt;em&gt;P. tentaculata&lt;/em&gt; was isolated from a young potted &lt;em&gt;Verbena&lt;/em&gt; hybrid, showing a collar and stalk rot, in a nursery in Majorca (Balearic Islands, Spain). It was initially recovered by plating ∼10&amp;nbsp;mm pieces of necrotic tissue from the leading lesion on to a phytophthora selective medium, P&lt;sub&gt;5&lt;/sub&gt;ARP (&lt;a class=&quot;referenceLink&quot; title=&quot;Link to bibliographic citation&quot; href=&quot;http://onlinelibrary.wiley.com.ezproxy.proxy.library.oregonstate.edu/doi/10.1111/j.1365-3059.2004.01089.x/full#b2&quot; rel=&quot;references:#b2&quot;&gt;Erwin &amp;amp; Ribeiro, 1996&lt;/a&gt;). A pure culture (isolate CBS 115458) was obtained by transferring aseptically a hyphal tip onto corn meal agar (CMA) and was first identified from morphological characters.&lt;/p&gt;&lt;/div&gt;&lt;div class=&quot;para&quot;&gt;&lt;p&gt;The colony surface texture was uniform and formed sparse, loosely branched mycelium on carrot piece agar (CPA: 50&amp;nbsp;g carrot pieces and 20&amp;nbsp;g agar per 1000&amp;nbsp;mL distilled water) and CMA. The radial growth rate was 2–3&amp;nbsp;mm&amp;nbsp;day&lt;sup&gt;−1&lt;/sup&gt; at 20°C on CMA. Sporangia did not appear on either agar media but formed readily in soil extract (50&amp;nbsp;g soil from a holm oak forest suspended in 1&amp;nbsp;L ionized water for 24 h at 20°C and then filtered and autoclaved). The sporangia were ovoid to globose, 27–52 (36·9)&amp;nbsp;×&amp;nbsp;17–31 (24·6) &lt;em&gt;µ&lt;/em&gt;m, length:breadth ratio 1·4, papillate with a narrow exit pore, and some were caducous with a short pedicel (&amp;lt;&amp;nbsp;5&amp;nbsp;&lt;em&gt;µ&lt;/em&gt;m). Hyphal swellings were present in water. Chlamydospores were only seen on CMA after 2 weeks. Oogonia, readily produced on CPA in pure culture, were globose, mostly terminal or a few lateral, and ranged from 17 to 41 (34·0) &lt;em&gt;µ&lt;/em&gt;m in diameter. Single paragynous, monoclinous or diclinous, usually long-stalked antheridia were club-shaped or spherical, 9–16 (12·7) &lt;em&gt;µ&lt;/em&gt;m in diameter and many had appendages. Occasionally two paragynous antheridia per oogonium, as well as some amphigynous antheridia, were observed. Oospores were aplerotic 16–33 (28·4)&amp;nbsp;&lt;em&gt;µ&lt;/em&gt;m in diameter and thin-walled.&lt;/p&gt;&lt;/div&gt;&lt;div class=&quot;para&quot;&gt;&lt;p&gt;To further confirm its identity, isozyme analysis based on malate dehydrogenase (EC 1.1.1.37) and malic enzymes (EC 1.1.1.40) was performed. Isozyme profiles fitted exactly those of three &lt;em&gt;P. tentaculata&lt;/em&gt; strains: two strains ex-&lt;em&gt;Chrysanthemum&lt;/em&gt; (including CBS 552.96 paratype) and one strain ex-&lt;em&gt;Verbena&lt;/em&gt;; and differing from those of all other papillate species (&lt;a class=&quot;referenceLink&quot; title=&quot;Link to bibliographic citations&quot; href=&quot;http://onlinelibrary.wiley.com.ezproxy.proxy.library.oregonstate.edu/doi/10.1111/j.1365-3059.2004.01089.x/full#b3&quot; rel=&quot;references:#b3 #b4&quot;&gt;Oudemans &amp;amp; Coffey, 1991a,b&lt;/a&gt;). Pathogenicity was assessed by flooding three potted &lt;em&gt;Verbena&lt;/em&gt; plants with a 10&lt;sup&gt;4&lt;/sup&gt; mL&lt;sup&gt;−1&lt;/sup&gt; zoospore suspension for 48 h at 20–22°C. As controls, two potted &lt;em&gt;Verbena&lt;/em&gt; plants were flooded with ionized water. Controls remained healthy 15&amp;nbsp;days after inoculation. All three inoculated &lt;em&gt;Verbena&lt;/em&gt; plants exhibited collar rot after 15&amp;nbsp;days, from which the pathogen was reisolated using PARP medium, thus confirming Koch's postulates. This is the first report of &lt;em&gt;P. tentaculata&lt;/em&gt; in Spain.&lt;/p&gt;&lt;/div&gt;&lt;/div&gt;</style></abstract><issue><style face="normal" font="default" size="100%">6</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, E.</style></author><author><style face="normal" font="default" size="100%">Descals, E.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Diplanetism and microcyclic sporulation in Phytophthora ramorum</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%">2011</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1111/j.1439-0329.2010.00674.x</style></url></web-urls></urls><number><style face="normal" font="default" size="100%">5</style></number><publisher><style face="normal" font="default" size="100%">Blackwell Publishing Ltd</style></publisher><volume><style face="normal" font="default" size="100%">41</style></volume><pages><style face="normal" font="default" size="100%">349–354</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 zoosporic phase of the pathogen &lt;em&gt;Phytophthora ramorum&lt;/em&gt; plays a crucial role in the process of plant infection, yet little is known about the fate of zoospores failing to target their hosts. Here, we describe new stages in the life cycle of &lt;em&gt;P. ramorum&lt;/em&gt; concerning the in vitro development of monomorphic diplanetism and microcyclic sporulation in free water. Papillate cysts were formed after zoospore suspensions of isolates of the EU1 and NA1 clonal lineages were vortexed. Cysts usually germinated directly forming an emerging tube, or indirectly by releasing a secondary zoospore, which leaves behind an empty cyst with a short evacuation tube. Germinate cysts frequently developed either an appressorium or a microsporangium both terminally. We also observed microcyclic sporulation, i.e. sporangia indirectly germinated by forming a microsporangium, as in microcyclic conidiation of true fungi. Temporal progress of encysted zoospores in solution showed that percentage of germination varied significantly among and within isolates as well as between experiments, suggesting that germination is partly ruled by internal mechanisms. Diplanetism and microcyclic sporulation in &lt;em&gt;P. ramorum&lt;/em&gt; may provide a second opportunity for host infection and may increase the chance of long dispersal in moving water.&lt;/p&gt;</style></abstract></record></records></xml>