CHANGES IN THE CHEMICAL DENUDATION INTENSITY IN THE RIVER PECHORA CATCHMENT UNDER THE INFLUENCE OF NON-STATIONARY CLIMATE AND ECONOMIC ACTIVITIES

Abstract

Introduction. Climate warming, which is currently observed in the Arctic, has the potential to intensify chemical denudation in river basins partially or completely located within permafrost. In order to test this hypothesis, we investigated the longterm dynamics of the rivers’ ion runoff in the Pechora River basin, 42 % of which are located within permafrost. Methods. To study changes in the chemical denudation intensity in nonstationary climate, we analyzed data of systematic observations over the main ion concentrations from 1985 to 2017 in the Pechora River outlet (Naryan-Mar) and its tributaries (Usa, Adzva, Kolva, Sula rivers). The intensity of chemical denudation in the Pechora River basin was assessed in terms of ion runoff. The probable reasons for its changes — water content and concentrations of macrocomponents — were also analyzed. Results. The ion-salt composition of Pechora River water is mainly determined by the dissolution of carbonate minerals in the underlying rocks. Calculations and comparison of ion runoff moduli showed that the studied rivers are comparable in terms of the chemical denudation intensity in catchments. The exceptions were the Sula and Kolva rivers, where, with the river runoff, a relatively high amount of chlorides and hydrocarbonates is carried. Contrary to the initial assumptions about the possible intensification of the chemical denudation process under the conditions of climate warming, we found a decrease in the sulfate runoff moduli in all rivers. In addition to that, individual changes in the runoff moduli for other main ions are observed for the studied rivers. Conclusion. In modern conditions, the chemical denudation intensity remains at the level of the end of the last century, and the long-term dynamics of the Pechora River ion runoff correlates in time with the variability of anthropogenic factors, in particular, wet sulfate deposition with atmospheric waters.