Atmospheric deposition of organic carbon via precipitation

AbstractAtmospheric deposition is the major pathway for removal of organic carbon (OC) from the atmosphere, affecting both atmospheric and landscape processes. Transfers of OC from the atmosphere to land occur as wet deposition (via precipitation) and as dry deposition (via surface settling of particles and gases). Despite current understanding of the significance of organic carbon inputs with precipitation to carbon budgets, transfers of organic matter between the atmosphere and land are not explicitly included in most carbon cycle models due to limited data, highlighting the need for further information. Studies regarding the abundance of OC in precipitation are relatively sparse, in part due to the fact that concentrations of organics in precipitation and their associated rates of atmospheric deposition are not routinely measured as a part of major deposition monitoring networks. Here, we provide a new data synthesis from 83 contemporary studies published in the peer reviewed literature where organic matter in precipitation was measured around the world. We compiled data regarding the concentrations of organic carbon in precipitation and associated rates of atmospheric deposition of organic carbon. We calculated summary statistics in a common set of units, providing insights into the magnitude and regional variability of OC in precipitation. A land to ocean gradient is evident in OC concentrations, with marine sites generally showing lower values than continental sites. Our synthesis highlights gaps in the data and challenges for data intercomparison. There is a need to concentrate sampling efforts in areas where anthropogenic OC emissions are on the rise (Asia, South America), as well as in remote sites suggesting background conditions, especially in Southern Hemisphere. It is also important to acquire more data for marine rainwater at various distances from the coast in order to assess a magnitude of carbon transfer between the land and the ocean. Our integration of the recent published information on OC in precipitation provides a unique data set (shared here as supplemental information) and a regional perspective that will be useful in carbon budgets, environmental modeling, and ecosystem studies. This can be used for comparison with past conditions and as a baseline toward exploring future changes, since changes in emissions, land use, and climatic variability are reflected in the amount and quality of OC deposited to ecosystems

Methylmercury in lake bed soils during re-flooding of an Appalachian reservoir in the northeastern USA

Mercury methylation, where inorganic mercury (Hg) is converted to methylmercury (MeHg), can increase in soils when flooded. While effects of the initial flooding of soils on MeHg production have been well studied, less is known about impacts of re-flooding on MeHg production. Lake Perez, an impounded recreational reservoir in the Appalachian Highlands, was completely drained then re-filled 7 years later. We use a combination of chemical, soil physical, and microbial data to quantify changes in MeHg before and after re-flooding of the lakebed. Portions that were transiently saturated due to pluvial flooding had the highest pre-flooded MeHg concentrations. When the lake was re-flooded, concentrations of MeHg in subaqueous soils increased by a factor of 2.74 (+174%) on average. Substantial variability was observed among the sampling sites, with smaller increases in MeHg at sites subjected to seasonal flooding during periods when the reservoir was drained. The increase of soil MeHg after re-flooding was lower in this study compared to studies that evaluated soil MeHg after initial flooding, indicating that re-flooding of a former lake bed caused a smaller response in MeHg production compared to initial flooding of terrestrial land. This study advances understanding of the environmental impact of impounded reservoirs

Variation of organic matter quantity and quality in streams at Critical Zone Observatory watersheds

The quantity and chemical composition of dissolved organic matter (DOM) in surface waters influence ecosystem processes and anthropogenic use of freshwater. However, despite the importance of understanding spatial and temporal patterns in DOM, measures of DOM quality are not routinely included as part of large-scale ecosystem monitoring programs and variations in analytical procedures can introduce artifacts. In this study, we used consistent sampling and analytical methods to meet the objective of defining variability in DOM quantity and quality and other measures of water quality in streamflow issuing from small forested watersheds located within five Critical Zone Observatory sites representing contrasting environmental conditions. Results show distinct separations among sites as a function of water quality constituents. Relationships among rates of atmospheric deposition, water quality conditions, and stream DOM quantity and quality are consistent with the notion that areas with relatively high rates of atmospheric nitrogen and sulfur deposition and high concentrations of divalent cations result in selective transport of DOM derived from microbial sources, including in-stream microbial phototrophs. We suggest that the critical zone as a whole strongly influences the origin, composition, and fate of DOM in streams. This study highlights the value of consistent DOM characterization methods included as part of long-term monitoring programs for improving our understanding of interactions among ecosystem processes as controls on DOM biogeochemistry