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Phytophthora Canker

Nickels Lab-Related Work On Lethal Phytophthora Canker, 1999

Greg T. Browne
USDA-ARS, Department of Plant Pathology
University of California, Davis

Introduction

This brief report on lethal Phytophthora canker (LPC) work provides an overview of experiments originally proposed for Nickels Estate but subsequently pursued in Kern County. The location change resulted from concern of the principal investigator over transporting the Phytophthora pathogens from Kern County to a commercial growing area in Northern California. Although Phytophthora cactorum and P. citricola are established in Northern California, it is unknown whether populations of these pathogens in Kern County are in some way unique or more virulent than the existing Northern California populations. Incidence of tree mortality caused by LPC has exceeded 6% in several Kern County orchards, but such losses are not currently documented in the northern almond districts. Research objectives pursued with support of the Almond Board include: 1) determining the causal agents of LPC, 2) determining parts of almond trees on which LPC infections occur, 3) determining sources of inoculum that contribute to LPC, and 4) developing appropriate control measures for LPC. Experiments summarized here relate only to portions of objectives 2) and 3). Complete interim and annual reports are available from the Almond Board.

Experiment on pre-infection control of LPC

An experiment was established in Kern County to determine the susceptibility of various tree parts to LPC infection and whether Bordeaux 10-10-100 mixture or Nutri-Phite sprays can protect against these infections. The chemical treatments were each applied to five replicate four-tree plots on 29 October (tree age approx. 12 yr) . Three weeks later the trees were inoculated on the trunk (by placing inoculum of P. citricola under a bark patch or on the surface of uninjured bark); in the scaffold crotch pocket (by placing the inoculum in the crotch, either with or without chisel-inflicted injuries to mimic growth cracks); and on scaffolds (by inoculating under a bark patch or on an uninjured latent bud). Control inoculations were conducted in the same way, but with sterile "inoculant". Assessment of treatment effects will be based on incidence and severity of cankers caused by P. citricola; the first assessment will occur in January 2000.

Experiments on post-infection control of LPC

Two experiments were conducted to evaluate post-infection efficacy chemical treatments for control of LPC. In the first test, P. citricola cankers were induced in a Kern County almond orchard by inoculating under bark patches on tree trunks and scaffold branches on 22 and 26 October. Controls received sterile inoculant. All sites inoculated with P. citricola developed cankers, but the controls remained healthy. On 1-3 December, canker size was measured, bark was prepared for post-infection treatments, and topical treatments were applied to the bark with paint brushes. The bark preparation treatments included 1) hatchet cuts that penetrated to the wood around canker margins, 2) surface bark removal around the canker margins, and 3) no treatment. The topical treatments included Aliette WDG® (1lb/gal), Ridomil Gold® (1 qt/3 gal), modified "magic elixir" (500 ml boiled linseed oil, 180 g basic CuSO4, 80 ml Hexol), and a non-treated control. Each treatment was applied to thoroughly wet the LPC-affected bark as well as adjacent tissue at least 10 cm beyond canker margins; healthy bark around the non-inoculated controls was treated at least 10 cm in all directions beyond the point of control inoculation. The first assessment of treatment efficacy will occur in January 2000.

For a second experiment on post-infection control of LPC, branch segments were cut from healthy trees, inoculated with P. citricola on 22 November in a greenhouse, and incubated in plastic bags (non-inoculated controls were included). On 27 November, cankers were measured, bark was prepared

for topical treatments, and the chemical mixtures described above painted on the branch segments. Bark-preparation treatments included 1) making chisel punctures into the wood at least 10 cm beyond the canker margins or 2) no treatment, as a control. Final canker dimensions were determined on 5 December. Each of the topical treatments suppressed canker expansion, and the chisel cuts in the bark improved efficacy of the elixer and Ridomil Gold (Fig. 1). After final canker measurements, pathogen isolations from the margins revealed that P. citricola was viable in all non-treated cankers and in most cankers treated with Aliette without pre-treatment bark cuts or elixer with or without the bark cuts, but the pathogen was usually not detected from cankers treated with Ridomil (Fig. 1). It appears that chemical treatments may aid post-infection control of LPC cankers, and additional work is planned to confirm the results and refine the treatments.

Fig. 1

Relative efficacy of three topical chemical treatments on post-infection control of cankers caused by Phytophthora citricola on excised branch segments. No significant necrosis occurred on noninoculated controls. Percentages indicate incidence of cankers from which P. citricola was culturable after the treatments and final canker measurements.

 

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Copyright © 1999 Colusa County Cooperative Extension, Univ. of California
Last modified: September 01, 2000