Sixteen days after a September wildfire, ethanol and water were measured in phloem and sapwood at breast height and the base of Pinus ponderosa Dougl. ex P. & C. Laws. with zero (control), moderate, heavy, and severe crown scorch. The quantity of ethanol increased with each level of injury, resulting in trees with severe scorch containing 15 and 53 times more phloem and sapwood ethanol, respectively, than controls. Ethanol concentrations in the sapwood and adjacent phloem were related, probably as a result of diffusion. Upward movement in xylem sap was most likely responsible for the relationship between sapwood ethanol concentrations at breast height and the stem base. As trees recovered from their heat injuries, the ethanol concentrations declined. In contrast, ethanol accumulated in dead trees that lost their entire crowns in the fire. Various bark and xylophagous beetles landed in greater numbers on fire-damaged trees than on controls the following spring and summer, suggesting that ethanol was being released to the atmosphere and influencing beetle behavior. Beetle landing was more strongly related to sapwood ethanol concentrations the previous September than in May. Sapwood ethanol measured 16 days after the fire was the best predictor of second-year mortality for trees with heavy and severe crown scorch.

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Roots from healthy and diseased mature ponderosa pine, Pinus ponderosa Laws., trees were excavated from a site near Burns, Oregon. The diseased trees were infected with black-stain root disease, Leptographium wageneri Kendrick, or annosus root disease, Heterobasidion annosum (Fr.) Bref., or both. Axial hydraulic conductivity of the roots was measured under a positive head pressure of 5 kPa, and the conducting area was stained with safranin dye to determine specific conductivity (k(s)). In diseased roots, only 8-12% of the cross-sectional xylem area conducted water. Resin-soaked xylem completely restricted water transport and accounted for 13-16% of the loss in conducting area. In roots with black-stain root disease, 17% of the loss in conducting area was associated with unstained xylem, possibly resulting from occlusions or embolisms. Based on the entire cross-sectional area of infected roots, the k(s) of roots infected with black-stain root disease was 4.6% of that for healthy roots, whereas the k(s) of roots infected with annosus root disease was 2.6% of that for healthy roots. Although these low values were partly the result of the presence of a large number of diseased roots (72%) with no conducting xylem, the k(s) of functional xylem of diseased roots was only 33% of that for healthy roots. The low k(s) values of functional xylem in diseased roots may be caused by fungus induced occlusions preceding cavitation and embolism of tracheids. The k(s) of disease-free roots from diseased trees was only 70% of that for healthy roots from healthy trees. The disease-free roots had the same mean tracheid diameter and tissue density as the healthy roots, suggesting that the lower k(s) in disease-free roots of diseased trees may also have been caused by partial xylary occlusions.

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