References

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Floria MP, Greslebin AG. ‘‘Mal del ciprés’’ disease: analysis of the association between aerial symptoms and vitality of trees. Phytophthoras in Forests and Natural Ecosystems. Proceedings of the Fourth Meeting of the International Union of Forest Research Organizations (IUFRO) Working Party. 2009 :282–3.
Webber J. Management of P. kernoviae and P. ramorum in southwest England. Goheen EM, Frankel SJ. Phytophthoras in Forests and Natural Ecosystems. 2009 ;General Technical Report PSW-GTR-221:177-183.
Ganley RJ, Williams NM, Rolando CA, Hood IA, Dungey HS, Beets PN, Bulman LS. Management of red needle cast, caused by Phytophthora pluvialis, a new disease of radiata pine in New Zealand. New Zealand Plant Protection [Internet]. 2014 ;67:48–53. Available from: http://www.nzpps.org/nzpp_abstract.php?paper=670480
Greenup M. Managing Chamaecyparis lawsoniana (Port-Orford-Cedar) to control the root disease caused by Phytophthora lateralis in the Pacific Northwest, USA. In: Coastally restricted forests. Coastally restricted forests. New York : Oxford University Press, 1998; 1998. pp. 93–100.
Hansen EM, Goheen DJ, Jules ES, Ullian B. Managing Port-Orford-Cedar and the Introduced Pathogen Phytophthora lateralis. Plant Disease [Internet]. 2000 ;84:4-14. Available from: http://apsjournals.apsnet.org/doi/abs/10.1094/PDIS.2000.84.1.4
Serrano MS, Osmundson T, Almaraz-Sanchez A, Croucher PJP, Swiecki T, Alvarado D, Garbelotto M. A microsatellite analysis identifies global pathways of movement of Phytophthora cinnamomi and the likely sources of wildland infestations in California and Mexico. Phytopathology [Internet]. 2019 . Available from: https://apsjournals.apsnet.org/doi/10.1094/PHYTO-03-19-0102-R
Ivors K, Garbelotto M, Vries IDE, Ruyter-Spira C, Hekkert TEB, Rosenzweig N, Bonants P. Microsatellite markers identify three lineages of Phytophthora ramorum in US nurseries, yet single lineages in US forest and European nursery populations. Molecular Ecology [Internet]. 2006 ;15:1493–1505. Available from: http://dx.doi.org/10.1111/j.1365-294X.2006.02864.x
Dale AL, Feau N, Everhart SE, Dhillon B, Wong B, Sheppard J, Bilodeau GJ, Brar A, Tabima JF, Shen D, et al. Mitotic Recombination and Rapid Genome Evolution in the Invasive Forest Pathogen Phytophthora ramorum Taylor JW. mBio [Internet]. 2019 ;10(2). Available from: https://mbio.asm.org/content/10/2/e02452-18
Henricot B, Pérez-Sierra A, Armstrong AC, Sharp PM, Green S. Morphological and genetic analyses of the invasive forest pathogen Phytophthora austrocedri reveal that two clonal lineages colonized Britain and Argentina from a common ancestral population. Phytopathology [Internet]. 2017 ;107(12):1532 - 1540. Available from: https://apsjournals.apsnet.org/doi/10.1094/PHYTO-03-17-0126-Rhttps://apsjournals.apsnet.org/doi/pdf/10.1094/PHYTO-03-17-0126-R
Blair JE, Coffey MD, Park S-Y, Geiser DM, Kang S. A multi-locus phylogeny for Phytophthora utilizing markers derived from complete genome sequences. Fungal Genetics and Biology [Internet]. 2008 ;45:266 - 277. Available from: http://www.sciencedirect.com/science/article/B6WFV-4PYP77J-1/2/ebf8754b49bc2fd36ab9e34941eeed43
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Garbelotto M, Schmidt D, Popenuck T. Pathogenicity and infectivity of Phytophthora ramorum vary depending on host species, infected plant part, inoculum potential, pathogen genotype, and temperature. Plant Pathology [Internet]. 2021 ;70(2):287 - 304. Available from: https://bsppjournals.onlinelibrary.wiley.com/doi/10.1111/ppa.13297
Greslebin AG, Hansen EM. Pathogenicity of Phytophthora austrocedrae on Austrocedrus chilensis and its relation with mal del ciprés in Patagonia. Plant Pathology [Internet]. 2010 ;59:604–612. Available from: http://dx.doi.org/10.1111/j.1365-3059.2010.02258.x
Dick M, Williams N, Bader M, Gardner J, Bulman L. Pathogenicity of Phytophthora pluvialis to Pinus radiata and its relation with red needle cast disease in New Zealand. New Zealand Journal of Forestry Science [Internet]. 2014 ;44(1):6. Available from: http://www.nzjforestryscience.com/content/44/1/6
Elliott M, Sumampong G, Varga A, Shamoun SF, James D, Masri S, Brière SC, Grünwald NJ. PCR-RFLP markers identify three lineages of the North American and European populations of Phytophthora ramorum. Forest Pathology [Internet]. 2009 ;39:266–278. Available from: http://dx.doi.org/10.1111/j.1439-0329.2008.00586.x
Elliott M, Sumampong G, Varga A, Shamoun SF, James D, Masri S, Grünwald NJ. Phenotypic differences among three clonal lineages of Phytophthora ramorum. Forest Pathology [Internet]. 2011 ;41:7–14. Available from: http://dx.doi.org/10.1111/j.1439-0329.2009.00627.x
Kasuga T, Kozanitas M, Bui M, Hüberli D, Rizzo DM, Garbelotto M. Phenotypic diversification Is associated with host-induced transposon derepression in the sudden oak death pathogen Phytophthora ramorum. PLoS ONE [Internet]. 2012 ;7:e34728. Available from: http://dx.doi.org/10.1371%2Fjournal.pone.0034728
Garbelotto MM, Schmidt DJ. Phosphonate controls sudden oak death pathogen for up to 2 years. California Agriculture [Internet]. 2009 ;63:10-17. Available from: http://ucanr.org/repository/cao/landingpage.cfm?article=ca.v063n01p10&fulltext=yes#
Ginetti B, Moricca S, Squires JN, Cooke DEL, Ragazzi A, Jung T. Phytophthora acerina sp. nov., a new species causing bleeding cankers and dieback of Acer pseudoplatanus trees in planted forests in northern Italy. Plant Pathology [Internet]. 2013 ;63(4):858–876. Available from: http://dx.doi.org/10.1111/ppa.12153

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