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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Two experiments were conducted to examine the influence of foliar nitrogen, terpenes, and phenolics of Douglas-fir on the development of gypsy moth larvae. In the first experiment, foliar concentrations of nitrogen and allelochemicals were manipulated by fertilizing 3-year-old potted seedlings with 0 or 200 ppm nitrogen. Concentrations of foliar nitrogen (0.33-2.38%) were negatively correlated with the phenolics (15.8-24.4 mg/g). Sixth-instar larvae previously reared on current-year Douglas-fir needles were allowed to feed on these seedlings. Pupal weights (312.8-995.6 mg) were positively correlated with levels of foliar nitrogen, negatively correlated with amounts of foliar phenolics, and uncorrelated with terpene concentrations. In the second experiment, terpene and phenolic extracts from Douglas-fir foliage were incorporated at natural levels into artificial diets with high and low levels of protein nitrogen. Neonate larvae grew faster and were larger on the high nitrogen control diet (4.1-4.5%), however, fourth instars performed better on the control diet with low nitrogen levels (2.5-2.7%). Foliar terpenes incorporated into diet had little effect on neonate fitness, but may induce subtle physiological changes in later instar larvae. Phenolics, alone or in combination with terpenes, excessively suppressed growth and survival, with no individuals living through the fourth instar, regardless of the nitrogen level. Incorporating foliar phenolic extracts into artificial diet caused unnatural levels of toxicity and failed to clarify the effects of Douglas-fir phenolics on gypsy moth fitness. Foliar nitrogen is a key factor influencing gypsy moth development on Douglas fir, but may be mitigated to some degree by phenolics.

This chapter argues that solutions to the management of invasive species need to be reworked to take into account the fact that invasive species can impact human livelihoods both negatively and positively. Besides the existing strategies for the management of invasive species, there is a need for alternative strategies in terms of the net benefit they yield, taking of course all benefits and costs into account. A specific case of control of invasive species in largely tropical landscapes is considered, with the attendant problems of human dependence on natural resources as well as lack of investment portfolios to control invasive species. Management strategies are proposed that promote use of the invasive as a way of minimizing the net costs of the invasive species.

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