Changes in soil organic matter and net nitrogen mineralization in heathland soils, after removal, addition or replacement of litter from Erica tetralix or Molinia caerulea.

The effects of different litter input rates and of different types of litter on soil organic matter accumulation and net N mineralization were investigated in plant communities dominated by Erica tetralix L. or Molinia caerulea (L.) Moench. Plots in which the litter on the soil had repeatedly been removed were compared with plots in the same plant community in which litter had been added to the soil. In another treatment, litter was removed and replaced by litter from the other plant community. Net N mineralization was measured in situ after 5 years. Less soil organic matter and soil N was found in plots in which litter had been removed, compared with control plots, or plots to which litter had been added, but these differences were significant for the Erica sp. soils only. Plots in which litter had been replaced and control plots did not differ significantly in the amount of soil organic matter. However, in both plant communities, the differences agreed with the faster decomposition rate of Molinia sp. litter compared with Erica sp. litter. The gravimetric soil moisture content was correlated positively with the amount of soil organic matter, both in the Erica sp. soils and the Molinia sp. soils. Net N mineralization rates (g N m-2) differed significantly between treatments for Erica sp. soils but no for Molinia sp. soils. For Erica sp. soils, net N mineralization rates increased with increasing amounts of soil organic matter and soil N. Replacing the litter with Molinia sp. litter (which differs in chemical composition) had no clear additional effect on the net N mineralization rate

Nitrogen Mineralization in Heathland Ecosystems Dominated by Different Plant-Species

Abstract Net N mineralization rates were measured in heathlands still dominated by ericaceous dwarf shrubs (Calluna vulgaris or Erica tetralix) and in heathlands that have become dominated by grasses (Molinia caerulea or Deschampsia flexuosa). Net N mineralization was measuredin situ by sequential soil incubations during the year. In the wet area (gravimetric soil moisture content 74–130%), the net N mineralization rates were 4.4 g N m–2 yr–1 in the Erica soil and 7.8 g N m–2 yr–1 in the Molinia soil. The net nitrification rate was negligibly slow in either soil. In the dry area (gravimetric soil moisture content 7–38%), net N mineralization rates were 6.2 g N M-2 yr–1 in the Calluna soil, 10.9 g N m–2 yr–1 in the Molinia soil and 12.6 g N m–2 yr–1 in the Deschampsia soil. The Calluna soil was consistently drier throughout the year, which may partly explain its slower mineralization rate. Net nitrification was 0.3 g N m–2 yr–1 in the Calluna soil, 3.6 g N m–2 yr–1 in the Molinia soil and 5.4 g N m–2 yr–1 in the Deschampsia soil. The net nitrification rate increased proportionally with the net N mineralization rate suggesting ammonium availability may control nitrification rates in these soils. In the dry area, the faster net N mineralization rates in sites dominated by grasses than in the site dominated by Calluna may be explained by the greater amounts of organic N in the soil of sites dominated by grasses. In both areas, however, the net amount of N mineralized per gram total soil N was greater in sites dominated by Molinia or Deschampsia than in sites dominated by Calluna or Erica. This suggests that in heathlands invaded by grasses the quality of the soil organic matter may be increased resulting in more rapid rates of soil N cycling

Nitrogen Mineralization in Heathland Ecosystems Dominated by Different Plant-Species

Abstract Net N mineralization rates were measured in heathlands still dominated by ericaceous dwarf shrubs (Calluna vulgaris or Erica tetralix) and in heathlands that have become dominated by grasses (Molinia caerulea or Deschampsia flexuosa). Net N mineralization was measuredin situ by sequential soil incubations during the year. In the wet area (gravimetric soil moisture content 74–130%), the net N mineralization rates were 4.4 g N m–2 yr–1 in the Erica soil and 7.8 g N m–2 yr–1 in the Molinia soil. The net nitrification rate was negligibly slow in either soil. In the dry area (gravimetric soil moisture content 7–38%), net N mineralization rates were 6.2 g N M-2 yr–1 in the Calluna soil, 10.9 g N m–2 yr–1 in the Molinia soil and 12.6 g N m–2 yr–1 in the Deschampsia soil. The Calluna soil was consistently drier throughout the year, which may partly explain its slower mineralization rate. Net nitrification was 0.3 g N m–2 yr–1 in the Calluna soil, 3.6 g N m–2 yr–1 in the Molinia soil and 5.4 g N m–2 yr–1 in the Deschampsia soil. The net nitrification rate increased proportionally with the net N mineralization rate suggesting ammonium availability may control nitrification rates in these soils. In the dry area, the faster net N mineralization rates in sites dominated by grasses than in the site dominated by Calluna may be explained by the greater amounts of organic N in the soil of sites dominated by grasses. In both areas, however, the net amount of N mineralized per gram total soil N was greater in sites dominated by Molinia or Deschampsia than in sites dominated by Calluna or Erica. This suggests that in heathlands invaded by grasses the quality of the soil organic matter may be increased resulting in more rapid rates of soil N cycling