PREDICTING RECOVERY IN ACIDIFIED FRESHWATERS BY THE YEAR 2010, AND BEYONDContract EVK1-1999-00087 - RECOVER:2010 Part of the 'Sustainable Management and Quality of Water' Ecosystem Functioning Directorate General Research |
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R.F. Wright1 and A. Jenkins2
1Norwegian Institute for Water Research,
P.O. Box 173, Kjelsås, N-0411 Oslo, Norway
2Centre for Ecology and Hydrology, Wallingford, Oxon OX10
8BB,UK
Full Reference
Wright, R.F. and Jenkins, A. (2001). Climate change as a confounding factor in reversibility of acidification: RAIN and CLIMEX projects. Hydrology and Earth System Sciences Vol. 5, No. 3, 379-390.
Introduction
This paper presents the precipitation and runoff data for the entire 17 year record from the roof experiment at Risdalsheia, and evaluated the confounding effect of climate variationsin reversibility of water acidification. Previous results from these experiments have been presented after one year of treatment (Wright et al., 1986), two years of treatment (Wright et al 1987), four years of treatment (Wright et al 1988), eight years of treatment (Wright et al 1993), and after three years of CLIMEX treatment (Wright et al., 1998)
The RAIN and CLIMEX experiments at Risdalsheia, southernmost Norway,
together cover 17 years (1984-2000) of whole-catchment manipulation of acid
deposition and climate. A 1200 m2roof placed over the forest canopy
at KIM catchment excluded about 80% of ambient acid deposition; clean rain was
sprinkled under the roof (Table 1). A climate change treatment
(3.7oC increase in air temperature and increase in air carbon
dioxide concentrations to 560 ppmv) was superimposed on the clean rain
treatment for four years (1995-1998). Sea-salt inputs and temperature are
climate-related factors that influence water chemistry and can confound
long-term trends caused by changes in deposition of sulphur and nitrogen. The
RAIN and CLIMEX experiments at Risdalsheia provided direct experimental data
that allow quantitative assessment of these factors.
Summary of results
Runoff chemistry responded rapidly to the decreased acid deposition.
Sulphate concentrations decreased by 50% within three years (Figure 1); nitrate
and ammonium concentrations decreased to new steady-state levels within the
first year (Figure 3). Acid neutralising capacity increased and hydrogen ion
aluminium decreased (Figure 4). Similar recovery from acidification was also
observed at the reference catchment ROLF, in response to the general 50%
reduction in sulphate deposition over southern Norway in the late 1980's and
1990s. Variations in sea-salt deposition caused large variations in run-off
chemistry at the reference catchment ROLF and the year-to-year noise in acid
neutralising capacity was as large as the overall trend over the period. These
variations were absent at KIM catchment because the sea-salt inputs were held
constant over the entire 17 years of the clean rain treatment. The climate
change experiment at KIM catchment resulted in increased leaching of inorganic
nitrogen, probably due to increased mineralisation and nitrification rates in
the soils.
Input-output budgets for SO4 show that KIM catchment released an average of c. 140 meq m-2 yr-1 of stored SO4 from the soil pool during the period 1985-1991 as the catchment adjusted to the new low level of SO4 inputs, this continued until the treatment stopped in 2000 (Figure 1).
Net release of SO4 also occurred at ROLF catchment in response to the decrease in ambient SO4 deposition during the 1990s. Cumulative loss was 60 meq m-2 yr-1 by 1994, about one-half the amount lost at KIM catchment.
Ammonia concentrations in run-off at KIM catchment also decreased in
response to the clean rain treatment and by 1990, concentrationswere less than
5 µeql-1. At ROLF catchment, NH4 concentrations
showed relatively large year-to-year variations but no significant trend in
NH4 deposition during this period
Under ambient conditions, before the clean rain treatment, KIM catchment retained about 50% of the incoming total N flux (Figure 3). Following the decrease in N deposition in 1984, the catchment continued to leak a similar proportion. At ROLF catchment, the net flux throughout the experimental period was very variable with a mean of c.60% retention. In 1995, with the start of the climate treatment at KIM catchment, both NO3 and NH4 concentrations in runoff increased relative to previous years, despite the fact that N deposition decreased |
The decreased concentrations of the strong acid anions SO4
and NO3 in runoff at KIM catchment through to 1994 was compensated
only slightly by a decrease in the sum of base cations (SBC) (Figure 2) and
mainly by an increase in ANC (Figure 4). Acid neutralising capacity showed a
rapid increase over the first five years, from c. -100 µeql-1
in 1984 to c. -20 µeql-1 in 1989, followed by a slower increase
to c. -5 µeql-1 in 1994. At ROLF catchment ANC also increased
from c. -90 µeql-1 in the late 1980s to c. -40
µeql-1 in 2000.
At KIM catchment, concentrations of of Al decreased from c. 10 to 2 µeql-1, while at ROLF catchment the decrease was 5 µeql-1(Figure 4).
References
Wright, R.F., 1987. Rain Project: Results after 2 years of treatment. In: Reversibility of Acidification (H. Barth (Ed.)), 14-49. Elsevier Applied Science, London.
Wright, R.F., 1998. Effect of increased CO2 and temperature on run-off chemistry at a forested catchment in southern Norway (CLIMEX project). Ecosystems, 1, 216-225.
Wright, R.F., Gjessing, E., Christophersen, N., Lotse, E., Seip, H.M., Semb, A., Sletaune, B., Storhaug, R. and Wedum, K., 1986. Project RAIN: changing acid deposition to whole catchments. The first year of treatment. Water Air Soil Pollut., 30, 47-63.
Wright, R.F., Lotse, E. and Semb, A., 1988. Reversibility of acidification shown by whole-catchment experiments. Nature, 334, 670-675. Wright, R.F., Lotse, E. and Semb, A., 1993. RAIN project: results after 8 years of experimentally reduced acid deposition. Can. J. Fisheries Aquat. Sci., 50, 258-268.