Rhizosphere, fine-root and needle chemistry were investigated in a 28 year old Norway spruce stand in SW Sweden. The uptake and allocation pattern of plant nutrients and aluminium in control plots (C) and plots repeatedly treated with ammonium sulphate (NS) were compared. Treatments started in 1988. Current year needles, one-year-old needles and cylindrical core samples of the LFH-layer and the mineral soil layers were sampled in 1988, 1989 and 1990. Compared to the control plots, pH decreased significantly in the rhizosphere soil in the NS plots in 1989 and 1990 while the SO4-S concentration increased significantly. Aluminium concentration in the rhizosphere soil was generally higher in the NS plots in all soil layers, except at 0-10 cm depths, both in 1989 and 1990. Calcium, Mg and K concentrations also increased after treatment with ammonium sulphate. Ammonium ions may have replaced these elements in the soil organic matter. The NS treatment significantly reduced Mg concentrations in fine roots in all layers in t990. A similar trend was found in the needles. Ca concentrations in fine roots were significantly lower in the NS plots in the LFH layer in 1990 and the same pattern was found in the current needles. The N and S concentrations of both fine roots and needles were significantly higher in the NS plots. It was suggested that NS treatment resulted in displacement of Mg, Ca and K from exchange sites in the LFH layer leading to leaching of these cations to the mineral soil. Further application of ammonium sulphate may damage the fine roots and consequently adversely affect the water and nutrient uptake of root systems.
Increased atmospheric deposition of N might eventually lead to P deficiency. The relation between needle P concentration and acid phosphatase activity in the humus layer was studied during 1990-93 in a Norway spruce stand where the water and N and P supplies had been experimentally manipulated since 1988. Treatments included control (C), yearly application of ammonium sulphate (NS), N-free fertilizer (V), granulated wood ash (A), irrigation (I), drought (D) and water plus nutrients in an "optimum" combination (IF). We found indications of a feed-back mechanism for P, where low concentrations in the needles were associated with increased acid phosphatase activity in the humus layer. Acid phosphatase estimations made during moist soil conditions were much more informative than those made during dry conditions. We further argue that a site-specific "base-line" exists for acid phosphatase activity in the soil, mainly originating from enzymes immobilized in the field, but active in the assay. Increased phosphatase activity, above the base line, was generally found in the A, I and NS treatments, but in some cases also in C. Although P and N concentrations were significantly higher in the IF treatment as compared to the C and the D treatments, the P as fraction of N was 0.10 and thus balanced in all cases. In the A and I treatment P:N was around 0.09, while it was only 0.07 in the NS treatment, mainly due to high N concentrations. The latter treatment thus created an imbalanced situation where P additions most likely would have increased tree growth.
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