Sammendrag
Substantial declines in acidifying emissions across Europe have led to pronounced chemical recovery of Norwegian surface waters. In recent decades, however, changes in water chemistry have increasingly coincided with climate change, complicating the attribution of observed trends to individual drivers. This study assesses whether ongoing climate change has produced detectable effects on freshwater chemistry in Norway and how these effects vary among catchments with differing sensitivities to acidification. In this study, the Model of Acidification of Groundwater In Catchments (MAGIC), which is based on current understanding of the processes governing acid–base chemistry in soils and waters, was used to simulate the effects of declining acid deposition. Deviations between observed and modelled water chemistry were provisionally interpreted as climate-related effects. However, these residuals may also reflect model or parameter uncertainty and other unaccounted-for processes. The analysis draws on long-term monitoring data (1986–2022) from 59 acid-sensitive Trend Lakes distributed across Norway, together with four Field Research Stations (1986–2020) representing contrasting hydroclimatic and biogeochemical conditions. Temporal trends were evaluated using the Mann–Kendall test and Sen’s slope estimator, while relationships between inferred climate effects and climatic variables were examined using Pearson’s correlation analysis. Across the Trend Lakes, inferred climate effects were predominantly positive for acid-neutralising capacity (ANC) and weathering-derived cations, suggesting that climate change may contribute to accelerated chemical recovery, particularly in catchments less sensitive to acidification. The inferred climate effects varied substantially among the Field Research Stations. Higher temperatures were generally associated with enhanced recovery, possibly through intensified silicate weathering, whereas increased precipitation and runoff appeared to dampen recovery. Overall, the results suggest that climate change exerts a measurable influence on freshwater chemistry in Norway, although the magnitude and direction of the response are strongly modulated by catchment-specific characteristics. While previous studies have identified climate-related influences on individual chemical variables, quantitative attempts to separate climate- and acid-deposition-related effects across a large number of acid-sensitive catchments remain rare. Here, we use deviations between observed water chemistry and MAGIC simulations of acid deposition recovery as a screening approach to investigate whether climate-related signals can be detected at the national scale and whether these signals vary among catchments with differing sensitivities to acidification.
Marianne Stave Sekkenes
Øyvind Kaste
Rolf David Vogt
Magnus Dahler Norling
Kari Austnes