Mexican devil [Ageratina adenophora (Spreng.) R.M. King & H. Rob.], a globally invasive weed with destructive effects on forests, has spread to numerous countries. To elucidate the inhibition of tree growth by A. adenophora, a study was conducted using the fungi (Lactarius deliciosus, Ceriporia lacerata, and Fomitopsis palustris) involved in the recycling of carbon and nutrients in forests. The focus was on investigating soil nitrogen and phosphorus availability in response to aqueous extracts from uncomposted and aerobically composted A. adenophora (EUA and ECA, respectively). The samples of composted A. adenophora from different sites exhibited a significant reduction in the concentration of allelochemicals 4,7-dimethyl-1-(propan-2-ylidene)-1,4,4a,8a-tetrahydronaphthalene-2,6(1H, 7H)-dione and 6-hydroxy-5-isopropyl-3,8-dimethyl-4a,5,6,7,8,8a-hexahydronaphthalen-2(1H)-one. This reduction more than 94% when compared with the concentration of these allelochemicals in CA. The EUA solutions at 5 and 10 mg L−1 (oven-dried plant biomass base) minimized L. deliciosus and C. lacerata growth, and significantly decreased F. palustris growth on the soil surface and within the soil. However, soil with ECA had no effect or promoting effect on the fungal growth. Compared with CK (only fungal inoculation in tested soil), the EUA solution reduced soil nitrogen and phosphorus, while ECA had the opposite effect; soil pH was increased by 0.01 to 0.08 under EUA treatment, while it decreased by 0.5 to 0.41under ECA treatment. Nitrogen and phosphorus availability were positively correlated with protease and phosphatase activity (r = 0.723 to 0.944), while available phosphorus was inversely correlated with pH in tested soils (r = -(0.809 to 0.978)). As such, the EUA solution decreased soil nitrogen and phosphorus supplies by inhibiting the liberation of proteases, phosphatases, and protons, which may lead to poor growth or even mortality of three fungal species. The in situ aerobically composted A. adenophora residues left behind may directly supply fungal species with nutrients and indirectly increase soil nutrient availability via the promotion of nitrogen and phosphorus mobilization.

Excess calcium intake has been shown to reduce growth and feed efficiency and to increase bone ash and bone strength in growing chickens. Source and level of dietary phosphorus have been shown to affect calcium tolerance. The effects of high calcium can be largely explained by its effects on intestinal pH. The proposed mechanism involves excess calcium reducing the soluble fraction of minerals and the proportion of minerals in small complexes. In consequence, their availability for absorption is probably also reduced. The growth depression of chickens fed on diets high in calcium may be partly caused by the decreased availability of other minerals needed for growth. Calcium tolerance of growing chickens may be increased by ensuring that there are higher than normal levels of the other required minerals in the diet.