Abstract

The geochemical and isotopic composition of surface water and groundwaters in the Velenje Basin, Slovenia, were investigated to gain a better understanding of the origin of surface and groundwaters. Surface waters and groundwaters from the Triassic aquifer are dominated by HCO3-, Ca2+, and Mg2+ from dissolution of carbonate minerals, while groundwaters from the Pliocene and Lithotamnium aquifers have distinct geochemical signatures, enriched in Na+ and K+. Surface waters are controlled by calcite dissolution, while groundwaters from the Triassic aquifer are controlled by dolomite dissolution. The partial pressure of CO2 in surface waters and groundwaters is well above atmospheric concentrations, indicating that these waters are a potential source of CO2 to the atmosphere. The δ13CDIC values of surface waters are shown to be controlled by biogeochemical processes in the terrestrial environment, such as dissolution of carbonates, degradation of organic matter, and exchange with atmospheric CO2, which is more pronounced in the lake waters. The δ13CDIC values of groundwater from the Triassic aquifer are consistent with degradation of CO2 and dissolution of dolomite. Groundwaters from the Pliocene and Lithotamnium aquifers have δ13CDIC values suggestive of biogenic CO2 reduction and degradation of organic matter.

Highlights

  • The geochemical study of river water allows important information to be obtained on chemical weathering of rocks and soil and the chemical and isotopic compositions of the drainage basin (GIBBS, 1972; REEDER et al, 1972; HU et al, 1982; STALLARD & EDMOND, 1983; GOLDSTEIN & JACOBSEN, 1987; ELDERFIELD et al, 1990; ZHANG et al, 1995; HUH et al, 1998)

  • 31 groundwaters were collected from Pliocene aquifers (16 samples from P11 and P12 aquifers), 13 groundwaters were collected from Triassic aquifers and 2 groundwaters were collected from Litotamnium aquifers

  • The major solute composition of surface waters in the Velenje Basin is dominated by HCO3, Ca2+ and Mg2+

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Summary

Introduction

The geochemical study of river water allows important information to be obtained on chemical weathering of rocks and soil and the chemical and isotopic compositions of the drainage basin (GIBBS, 1972; REEDER et al, 1972; HU et al, 1982; STALLARD & EDMOND, 1983; GOLDSTEIN & JACOBSEN, 1987; ELDERFIELD et al, 1990; ZHANG et al, 1995; HUH et al, 1998). The use of stable isotopes of carbon as an additional method is crucial to evaluate biogeochemical processes in rivers (BRUNKE & GAUSER, 1997; SOPHACLEOUS, 2002; WACHINEW, 2006). Many hydrogeological studies use stable isotopes of the water molecule to determine groundwater quality, origin, recharge mechanisms, and rock-water interactions. The isotopic characterization of the groundwater is needed to fully evaluate the processes and origin of gases in coal basins (ARAVENA et al, 2003)

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