Critical loads of acidity for surface waters in south-central Ontario, Canada: regional application of the Steady-State Water Chemistry (SSWC) model

2002 ◽  
Vol 59 (8) ◽  
pp. 1287-1295 ◽  
Author(s):  
A Henriksen ◽  
P J Dillon ◽  
J Aherne

Critical loads of acidity and the amount by which these critical loads are exceeded by atmospheric deposition (termed "exceedances") were estimated for 1469 lakes from five regions in south-central Ontario, Canada, using single lake chemistry measurements and sulphur deposition data for the period 1976–1999. Based on the Steady-State Water Chemistry (SSWC) model, four of the five regions had low critical loads, which is consistent with the underlying geology (silicate bedrock) and the thin glacial soils in these regions. Sulphur deposition in the study area showed a clear downward trend over the time period, with a decrease of approximately 50% to current levels of approximately 44 meq·m–2·year–1. As a result of the declining deposition, the portion of lakes with critical load exceedances has dropped substantially, from 74–82% in the four sensitive regions in 1976 to 11–26% in 1999. The pentile critical load is typically used as a regional target to account for uncertainties, but also to ensure that a sufficient percentage of lakes are protected (95%). This suggests that further reductions in emissions are required to reduce depositions to approximately 34 meq·m–2·year–1 (11 kg S·ha–1·year–1) to prevent critical load exceedance.

1993 ◽  
Vol 1 (2) ◽  
pp. 145-156 ◽  
Author(s):  
L. H. Pardo ◽  
C. T. Driscoll

Critical loads are used in the assessment of air pollution and regulation of the causative emissions to prevent or mitigate ecological damage. We critically review four mass balance methods for calculating critical loads for nitrogen deposition: the steady-state water chemistry method, the nitrogen mass balance method, the basic cation mass balance method, and the steady-state mass balance method. The critical loads may be calculated with respect to effects of acidification associated with nitrate leaching or effects of elevated nitrogen such as eutrophication, excess nitrate loss, and nutrient imbalances. The most useful method for calculating the critical load for nitrogen with respect to effects of elevated atmospheric deposition of nitrogen is the nitrogen mass balance method. The steady-state water chemistry method can be readily applied for regional-scale calculations because it requires only water chemistry data from synoptic surveys of surface waters and does not explicitly consider biogeochemical processes. Both of the other approaches are severely limited by lack of quantitative information on rates of mineral weathering. If weathering data were available, the steady-state mass balance method could be more effectively used to assess critical loads with respect to acidification. Similarly, the basic cation mass balance method could be used to calculate critical loads for both acidity and elevated nitrogen effects. Because of the complexity of the nitrogen cycle, it is not possible to obtain a single critical load for the whole ecosystem. Rather, one should analyze and synthesize several values of critical loads that reflect different components of the ecosystem and different ecological effects of elevated nitrogen deposition (e.g., acidification and eutrophication effects).Key words: atmospheric deposition of nitrogen, acidification, critical loads, nitrogen cycling.


2008 ◽  
Vol 65 (5) ◽  
pp. 821-833 ◽  
Author(s):  
Shaun A Watmough ◽  
Julian Aherne

Calcium (Ca) concentrations in surface waters on the Precambrian Shield are determined primarily by the Ca weathering rate in soil, which requires extensive soil data that generally do not exist. From a water chemistry database comprising approximately 550 lakes in south-central Ontario, Canada, 130 lakes were selected with low Ca concentrations (Ca < 75 µmol·L–1). Calcium weathering is primarily dominated by silicate minerals such as plagioclase and hornblende, allowing the use of Ca–sodium (Na) ratios in lake water to estimate Ca weathering rates. Soil profile data at seven sites indicated that the Ca–Na ratio from mineral weathering is 0.86; correspondingly, Ca weathering rates in lakes ranged from 0.04 to 0.24 kmol·ha–1·year–1 (median of 0.09 kmol·ha–1·year–1). This compares with a range of 0.06–0.24 kmol·ha–1·year–1 (median of 0.14 kmol·ha–1·year–1) obtained using the steady-state water chemistry model. Using these methods to bound potential weathering rates, Ca concentrations in individual lakes at steady state are predicted to decline by 10%–40% compared with current values. Dynamic soil hydrochemical model predictions indicate that Ca concentrations in lakes will be considerably lower than these steady-state predictions within decades if timber harvesting occurs in the drainage basins.


2018 ◽  
Author(s):  
Paul A. Makar ◽  
Ayodeji Akingunola ◽  
Julian Aherne ◽  
Amanda S. Cole ◽  
Yayne-abeba Aklilu ◽  
...  

Abstract. Estimates of potential harmful effects to ecosystems in the Canadian provinces of Alberta and Saskatchewan due to acidifying deposition were calculated, using a one year simulation of a high resolution implementation of the Global Environmental Multiscale – Modelling Air-quality and Chemistry (GEM-MACH) model, and estimates of aquatic and terrestrial ecosystem critical loads. The model simulation was evaluated against two different sources of deposition data; total deposition in precipitation and total deposition to snowpack in the vicinity of the Athabasca oil sands. The model captured much of the variability of observed ions in wet deposition in precipitation (observed versus model sulphur, nitrogen and base cation R2 values of 0.90, 0.76 and 0.72, respectively), while being biased high for sulphur deposition, and low for nitrogen and base cations (slopes 2.2, 0.89 and 0.40, respectively). Aircraft-observation-based estimates of fugitive dust emissions, shown to be a factor of ten higher than reported values (Zhang et al., 2017), were used to estimate the impact of increased levels of fugitive dust on model results. Model comparisons to open snowpack observations were shown to be biased high, but in reasonable agreement for sulphur deposition when observations were corrected to account for throughfall in needleleaf forests. The model-observation relationships for precipitation deposition data, along with the expected effects of increased (unreported) base cation emissions, were used to provide a simple observation-based correction to model deposition fields. Base cation deposition was estimated using published observations of base cation fractions in surface collected particles (Wang et al., 2015). Both original and observation-corrected model estimates of sulphur, nitrogen and base cation deposition were used in conjunction with critical load data created using the NEG-ECP (2001) and CLRTAP (2004, 2016, 2017) protocols for critical loads, using variations on the Simple Mass Balance model for forest and terrestrial ecosystems, and the Steady State Water Chemistry and the First-order Acidity Balance models for aquatic ecosystems. Potential ecosystem damage at 2013/14 emissions and deposition levels was predicted for regions within each of the ecosystem critical load datasets examined here. The spatial extent of the regions in exceedance of critical loads varied between 1 × 104 and 3.3 × 105 km2, for the more conservative observation-corrected estimates of deposition, with the variation dependant on the ecosystem and critical load protocol. The larger estimates (for aquatic ecosystems) represent a substantial fraction of the area of the provinces examined. Base cation deposition was shown to have a neutralizing effect on acidifying deposition, and the use of the aircraft and precipitation observation-based corrections to base cation deposition resulted in reasonable agreement with snowpack data collected in the oil sands area. However, critical load exceedances calculated using both observations and observation-corrected deposition suggest that the neutralization effect is limited in spatial extent, decreasing rapidly with distance from emissions sources, due to the rapid deposition of emitted primary particles dust particles as a function of their size.


2000 ◽  
Vol 4 (1) ◽  
pp. 125-140 ◽  
Author(s):  
C. Curtis ◽  
T. Allott ◽  
J. Hall ◽  
R. Harriman ◽  
R. Helliwell ◽  
...  

Abstract. The critical loads approach is widely used within Europe to assess the impacts of acid deposition on terrestrial and freshwater ecosystems. Recent work in Great Britain has focused on the national application of the First-order Acidity Balance (FAB) model to a freshwaters dataset of 1470 lake and stream water chemistry samples from sites across Britain which were selected to represent the most sensitive water bodies in their corresponding 10 km grid square. A ``Critical Load Function" generated for each site is compared with the deposition load of S and N at the time of water chemistry sampling. The model predicts that when catchment processes reach steady-state with these deposition levels, increases in nitrate leaching will depress acid neutralizing capacity (ANC) below the critical threshold of 0 μeql-1 at more than a quarter of the sites sampled, i.e. the critical load of acid deposition is exceeded at these sites. The critical load exceedances are generally found in upland regions of high deposition where acidification has been previously recognised, but critical loads in large areas of western Scotland are also exceeded where little biological evidence of acidification has yet been found. There is a regional variation in the deposition reduction requirements for protection of the sampled sites. The FAB model indicates that in Scotland, most of the sampled sites could be protected by sufficiently large reductions in S deposition alone. In the English and Welsh uplands, both S and N deposition must be reduced to protect the sites. Current international commitments to reduce S deposition throughout Europe will therefore be insufficient to protect the most sensitive freshwaters in England and Wales. Keywords: critical loads; acidification; nitrate; FAB model; acid deposition


2003 ◽  
Vol 60 (9) ◽  
pp. 1095-1103 ◽  
Author(s):  
S A Watmough ◽  
J Aherne ◽  
P J Dillon

The potential impact of harvesting on lake chemistry was assessed for ~1300 lakes in south-central Ontario using a critical loads approach based on the steady-state water chemistry (SSWC) model. The critical load of acidity is currently only exceeded by bulk sulphate deposition in 9% of the lakes if harvesting does not occur. However, the percentage increases to 23%, 56%, and 72% under potential harvesting scenarios that assume wood-only (stem without bark), stem-only, or whole-tree harvesting, respectively. This increase in exceedance of critical load is due to the much lower base cation concentrations in lakes resulting from base cation removals during harvest. For example, only 0.3% of lakes will have Ca2+ concentrations <50 μequiv.·L–1 if harvesting does not occur, whereas 52% of lakes will have Ca2+ concentrations <50 μequiv.·L–1 if whole-tree harvesting occurs. Harvesting clearly has an enormous potential impact on lake chemistry, which will become more apparent as exchangeable base cation pools in soil decline and acid inputs can no longer be buffered.


2003 ◽  
Vol 33 (8) ◽  
pp. 1544-1556 ◽  
Author(s):  
Shaun A Watmough ◽  
Peter J Dillon

We calculated critical loads of acidity (S and S + N separately) for seven forested catchments in south-central Ontario, using a critical threshold designed to maintain the Ca/Al molar ratio above 1.0 or the base cation (BC; Ca + Mg + K) to Al molar ratio above 10 in soil solution. Critical loads are ~10–50% lower using the BC/Al ratio compared with the Ca/Al ratio, and harvesting greatly increases forest sensitivity to acid deposition. If forests are harvested, critical load calculations indicate that further reductions in S and N bulk deposition are required to maintain the BC/Al ratio in soil solution above 10, but reductions in S deposition are only mandatory for three of the seven catchments. However, S export exceeds inputs in bulk deposition by 40–100%. Our study indicates that setting the critical threshold of BC/Al at 10 may not maintain soil base saturation above 20%, and that N export is unpredictable at current deposition levels. We calculate that SO4 leaching (and therefore deposition) must be reduced by between 10 and 74% to maintain healthy, productive forests in catchments that are harvested. More reliable estimates of base cation removals during harvest, minimum Ca leaching losses from soils that can occur without affecting forest productivity, and critical limits for soil base saturation are needed to improve these critical load estimates.


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