Abstract

In this study, the influence of temperature and vegetation cover on soluble inorganic and organic nitrogen in a spodosol from north east Scotland was investigated. Firstly, soil cores were incubated at 5, 10 and 15°C for up to 8 weeks. Net mineralisation was observed at all temperatures with larger rates observed at higher temperatures. In contrast, water extractable dissolved organic nitrogen (DON) displayed no clear trend with time and showed little response to temperature. Secondly, intact cores of the same soil, with and without vegetation, were leached with artificial rain for 6 weeks at 6.5 and 15°C. Temperature and the presence of vegetation interacted to have a significant (P<0.01) effect on the concentration of NO3− in leachates; highest concentrations were observed in leachates from cores without vegetation at 15°C, whereas lowest concentrations were observed in leachates from cores with vegetation at 6.5°C. In contrast, concentrations of DON and dissolved organic carbon (DOC) were significantly (P<0.001) higher in leachates from cores with vegetation than without vegetation and were not affected by temperature. The cumulative amounts of DON and DOC leached from the cores with vegetation were 4 and 2.5 times greater, respectively, than those leached from the cores without vegetation. Comparison of soil solution (extracted by centrifugation at 0–5 and 5–10cm depth) after leaching for 6 weeks, showed that the upper layer contained more than twice the amount of DON than the 5–10cm layer and that the difference in concentration between the two depths was enhanced in the presence of vegetation. The results indicate that vegetation is an important source of DON and DOC. However, the removal of vegetation did not lead to an increase in the quantity of total dissolved nitrogen (TDN) in soil water, but resulted in a change in the dominant N fraction from DON to NO3−. In addition, the results show that DON, in both the incubated and leached cores, did not change as inorganic N was mineralised. This suggests that if water extractable DON was acting as a source of NH4+ or NO3−, then it was being replenished by, and in equilibrium with, a large reserve of organic N. Evidence of such a pool was indirect in the form of additional DON (equivalent to 2gNm−2) being extracted by 0.5M K2SO4.

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