Isotopic signatures of N2O are increasingly used to constrain the total global flux and the relative contribution of nitrification and denitrification to N2O emissions. Interpretation of isotopic signatures of soil-emitted N2O can be complicated by the isotopic effects of gas diffusion. The aim of our study was to measure the isotopic fractionation factors of diffusion for the isotopologues of N2O and to estimate the potential effect of diffusive fractionation during N2O fluxes from soils using simple simulations. Diffusion experiments were conducted to monitor isotopic signatures of N2O in reservoirs that lost N2O by defined diffusive fluxes. Two different mathematical approaches were used to derive diffusive isotope fractionation factors for 18O (epsilon18O), average 15N (epsilonbulk) and 15N of the central (alpha(-)) and peripheral (beta(-)) position within the linear N2O molecule (epsilon15Nalpha, epsilon15Nbeta). The measured epsilon18O was -7.79 +/- 0.27 per thousand and thus higher than the theoretical value of -8.7 per thousand. Conversely, the measured epsilonbulk (-5.23 +/- 0.27 per thousand) was lower than the theoretical value (-4.4 per thousand). The measured site-specific 15N fractionation factors were not equal, giving a difference between epsilon15Nalpha and epsilon15Nbeta (epsilonSP) of 1.55 +/- 0.28 per thousand. Diffusive fluxes of the N2O isotopologues from the soil pore space to the atmosphere were simulated, showing that isotopic signatures of N2O source pools and emitted N2O can be substantially different during periods of non-steady state fluxes. Our results show that diffusive isotope fractionation should be taken into account when interpreting natural abundance isotopic signatures of N2O fluxes from soils.
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http://dx.doi.org/10.1002/rcm.3656 | DOI Listing |
J Hazard Mater
January 2025
Dept. of Science Education, Ewha Womans University, Seoul 03760, South Korea. Electronic address:
Although sulfur-bearing minerals are valuable resources, they pose significant environmental risks to river ecosystems by releasing hazardous leachate. Accurately tracing these sources is crucial but challenging due to overlapping chemical signatures and pollutant transport dynamics in river systems. This study investigates seasonal and spatial variations in sulfate (SO) and trace element contributions in mining districts of the upper Nakdong River basin, South Korea.
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US Geological Survey, New England Water Science Center, Northborough, MA, USA.
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December 2024
Andean Geothermal Center of Excellence, University of Chile, Santiago 8370446, Chile.
We used otolith chemistry to test and complement current hypotheses regarding habitat use and connectivity between sub-populations in Area 48 of the Commission for the Conservation of Antarctic Marine Living Resources (CCAMLR). Sagittal otoliths from 45 fish sampled near the South Orkney Islands were analysed. Their elemental (Li, Na, Mg, Cr, Mn, Sr, Sn, and Ba relative to Ca) and isotopic (δO and δC) signatures were examined in both the nuclear and marginal regions, representing juvenile and adult stages.
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Universidad de Navarra, Instituto de Biodiversidad y Medioambiente BIOMA, Irunlarrea 1, 31008 Pamplona, Spain.
J Environ Sci (China)
July 2025
Geology Institute of China Chemical Geology and Mine Bureau, Beijing 100101, China; Technology Innovation Center for Ecological Restoration Engineering in Mining Area, Ministry of Natural Resources, Beijing 100083, China.
Contaminants in the water environment of different pyrite mines have varying characteristics due to different geological origins. Sulfur isotope (δS) is an effective tool to reveal the mechanism of water environment contamination, but no investigations have yet analyzed the characteristics and environmental significance of the δS in the water environment of different pyrite mines. This study involved a field investigation of four typical pyrite mines in China (representing volcanic, skarn, sedimentary-metamorphic, and coal-deposited types) and the analysis of the hydrochemistry of aqueous samples and the δS of both pyrite and dissolved sulfates.
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