scholarly journals Nitrogen saturation of forested catchments in central Japan - Progress or recovery?

Author(s):  
Hiroyuki Sase ◽  
Masamichi Takahashi ◽  
Kazuhide Matsuda ◽  
Naoyuki Yamashita ◽  
Urumu Tsunogai ◽  
...  
2018 ◽  
Author(s):  
Fumiko Nakagawa ◽  
Urumu Tsunogai ◽  
Yusuke Obata ◽  
Kenta Ando ◽  
Naoyuki Yamashita ◽  
...  

Abstract. To clarify the biological processing of nitrate within temperate forested catchments using unprocessed atmospheric nitrate exported from each catchment as a tracer, we continuously monitored stream nitrate concentrations and stable isotopic compositions including 17O-excess (Δ17O) in three forested catchments in Japan (KJ, IJ1, and IJ2) for more than two years. The catchments showed varying flux-weighted average nitrate concentrations: 58.4, 24.4, and 17.1 µmol L−1 in KJ, IJ1, and IJ2, respectively. In addition to stream nitrate, nitrate concentrations and stable isotopic compositions in soil water were determined for comparison in the most nitrate-enriched catchment (the KJ site). While 17O-excess of nitrate in soil water showed significant seasonal variation, ranging from +0.1 to +5.7 ‰, stream nitrate showed small variation, from +0.8 to +2.0‰ in KJ, +0.7 to +2.8 ‰ in IJ1, and +0.4 to +2.2‰ in IJ2. We concluded that the major source of stream nitrate in each forested catchment was nitrate in groundwater, which buffered the seasonal variations in soil water nitrate. The estimated annual export flux of unprocessed atmospheric nitrate accounted for 9.4 ± 2.6 %, 6.5 ± 1.8 %, and 2.6 ± 0.6 % of the annual deposition flux of atmospheric nitrate in KJ, IJ1, and IJ2, respectively. The export flux of unprocessed atmospheric nitrate relative to the deposition flux showed a clear normal correlation with the flux-weighted average concentration of stream nitrate, indicating that reductions in the biological assimilation rates of nitrate in forested soils, rather than increased nitrification rates, are likely responsible for the enrichment of stream nitrate, probably due to nitrogen saturation. The export flux of unprocessed atmospheric nitrate relative to the deposition flux in each forest ecosystem is applicable as an index for nitrogen saturation.


2001 ◽  
Vol 5 (3) ◽  
pp. 379-390 ◽  
Author(s):  
M. Rogora ◽  
A. Marchetto ◽  
R. Mosello

Abstract. The Lake Maggiore catchment is the area of Italy most affected by acid deposition. Trend analysis was performed on long-term (15-30 years) series of chemical analyses of atmospheric deposition, four small rivers draining forested catchments and four high mountain lakes. An improvement in the quality of atmospheric deposition was detected, due to decreasing sulphate concentration and increasing pH. Similar trends were also found in high mountain lakes and in small rivers. Atmospheric deposition, however, is still providing a large and steady flux of nitrogen compounds (nitrate and ammonium) which is causing increasing nitrogen saturation in forest ecosystems and increasing nitrate levels in rivers. Besides atmospheric deposition, an important factor controlling water acidification and recovery is the weathering of rocks and soils which may be influenced by climate warming. A further factor is the episodic deposition of Saharan calcareous dust which contributes significantly to base cation deposition. Keywords: trend, atmospheric deposition, nitrogen, stream water chemistry.


2018 ◽  
Vol 15 (22) ◽  
pp. 7025-7042 ◽  
Author(s):  
Fumiko Nakagawa ◽  
Urumu Tsunogai ◽  
Yusuke Obata ◽  
Kenta Ando ◽  
Naoyuki Yamashita ◽  
...  

Abstract. To clarify the biological processing of nitrate within temperate forested catchments using unprocessed atmospheric nitrate exported from each catchment as a tracer, we continuously monitored stream nitrate concentrations and stable isotopic compositions, including 17O excess (Δ17O), in three forested catchments in Japan (KJ, IJ1, and IJ2) for more than 2 years. The catchments showed varying flux-weighted average nitrate concentrations of 58.4, 24.4, and 17.1 µmol L−1 in KJ, IJ1, and IJ2, respectively, which correspond to varying export fluxes of nitrate: 76.4, 50.1, and 35.1 mmol m−2 in KJ, IJ1, and IJ2, respectively. In addition to stream nitrate, nitrate concentrations and stable isotopic compositions in soil water were determined for comparison in the most nitrate-enriched catchment (site KJ). While the 17O excess of nitrate in soil water showed significant seasonal variation, ranging from +0.1 ‰ to +5.7 ‰ in KJ, stream nitrate showed small variation, from +0.8 ‰ to +2.0 ‰ in KJ, +0.7 ‰ to +2.8 ‰ in IJ1, and +0.4 ‰ to +2.2 ‰ in IJ2. We conclude that the major source of stream nitrate in each forested catchment is groundwater nitrate. Additionally, the significant seasonal variation found in soil nitrate is buffered by the groundwater nitrate. The estimated annual export flux of unprocessed atmospheric nitrate accounted for 9.4 %±2.6 %, 6.5 %±1.8 %, and 2.6 %±0.6 % of the annual deposition flux of atmospheric nitrate in KJ, IJ1, and IJ2, respectively. The export flux of unprocessed atmospheric nitrate relative to the deposition flux showed a clear normal correlation with the flux-weighted average concentration of stream nitrate, indicating that reductions in the biological assimilation rates of nitrate in forested soils, rather than increased nitrification rates, are likely responsible for the elevated stream nitrate concentration, probably as a result of nitrogen saturation. The export flux of unprocessed atmospheric nitrate relative to the deposition flux in each forest ecosystem is applicable as an index for nitrogen saturation.


2016 ◽  
Vol 50 (3) ◽  
pp. 227-239 ◽  
Author(s):  
Muga Yaguchi ◽  
Yoichi Muramatsu ◽  
Hitoshi Chiba ◽  
Fumiaki Okumura ◽  
Takeshi Ohba
Keyword(s):  

Sign in / Sign up

Export Citation Format

Share Document