Ed Roland
Addicted to ArboristSite
As you know, WW, I am a fan of this technique, but I don't believe the 160 deg temperatures in farenheit you stated would be sufficient. Where this would kill the contacted pathogen, it would not, IMO, sufficiently alter the remaining wood structure to prevent reinfection. Pathogens, by the hundreds, are ubiquitous with the phyllosphere. They will be there to some degree or another and can become opportunistic (apparently on a whim) so my thought would be to alter the freshly excised tissues with fire hardening.
Not exactly a new concept. Prehistoric man had this figured out, even witout citations.
At approximately 300 deg F, cellulose starts to degrade. That's the little puff of smoke you see. Lignin, being a polymer, folds back on itself and bonds with the other remaining chemicals available within the tree (phenols, resins, etc). This creates a zone of altered cells much less suitable for infection.
So in the case of localized infections this technique may hold a lot of promise.
Dave
I hear you Dave. Altering the wood under the canker to be less hospitable for reinfection may hold a lot of promise. But, do we want to be so intrusive and damaging to the tree by introducing 300 deg f when 130-160 deg f will sufficiently treat these localized areas?
SOLARIZATION OF PEAR AND APPLE TREES TO ERADICATE BACTERIA IN FIRE BLIGHT CANKERS @ ://www.actahort.org/members/showpdf?booknrarnr=411_68 "raised temperatures inside the tents to 56°C, resulting in complete eradication of the pathogen and death of tops of the trees."
56 c = 132.8 f
If a polymer may be the answer then perhaps we can try treating the excision with our samples of sodium silicate.