scholarly journals Isotopic and chromatographic fingerprinting of the sources of dissolved organic carbon in a shallow coastal aquifer

2020 ◽  
Vol 24 (4) ◽  
pp. 2167-2178 ◽  
Author(s):  
Karina T. Meredith ◽  
Andy Baker ◽  
Martin S. Andersen ◽  
Denis M. O'Carroll ◽  
Helen Rutlidge ◽  
...  

Abstract. The terrestrial subsurface is the largest source of freshwater globally. The organic carbon contained within it and processes controlling its concentration remain largely unknown. The global median concentration of dissolved organic carbon (DOC) in groundwater is low compared to surface waters, suggesting significant processing in the subsurface. Yet the processes that remove this DOC in groundwater are not fully understood. The purpose of this study was to investigate the different sources and processes influencing DOC in a shallow anoxic coastal aquifer. Uniquely, this study combines liquid chromatography organic carbon detection with organic (δ13CDOC) carbon isotope geochemical analyses to fingerprint the various DOC sources that influence the concentration, carbon isotopic composition, and character with respect to distance from surface water sources, depth below surface, and inferred groundwater residence time (using 3H activities) in groundwater. It was found that the average groundwater DOC concentration was 5 times higher (5 mg L−1) than the global median concentration and that the concentration doubled with depth at our site, but the chromatographic character did not change significantly. The anoxic saturated conditions of the aquifer limited the rate of organic matter processing, leading to enhanced preservation and storage of the DOC sources from peats and palaeosols contained within the aquifer. All groundwater samples were more aromatic for their molecular weight in comparison to other lakes, rivers and surface marine samples studied. The destabilization or changes in hydrology, whether by anthropogenic or natural processes, could lead to the flux of up to 10 times more unreacted organic carbon from this coastal aquifer compared to deeper inland aquifers.

2019 ◽  
Author(s):  
Karina T. Meredith ◽  
Andy Baker ◽  
Martin S. Andersen ◽  
Denis M. O'Carroll ◽  
Helen Rutlidge ◽  
...  

Abstract. The terrestrial sub-surface is the largest source of freshwater globally. The organic carbon contained within it and processes controlling its concentration remain largely unknown. The global median concentration of dissolved organic carbon in groundwater is low compared to surface waters suggesting significant processing in the subsurface. Yet the processes that remove this dissolved organic carbon (DOC) in groundwater are not fully understood. The purpose of this study was to investigate the different sources and processes influencing DOC in a shallow anoxic coastal aquifer. Uniquely, this study combines liquid chromatography organic carbon detection with inorganic (δ13CDIC) and organic (δ13CDOC) carbon isotope geochemical analyses, to fingerprint the various DOC sources that influence the concentration, carbon isotopic composition and character with distance from surface water sources, depth below surface and groundwater residence time (using 3H) in groundwater. It was found that the average groundwater DOC concentration was five times higher (5 mg L−1) than the global median concentration and it doubled with depth, but the chromatographic character did not change significantly. The anoxic saturated conditions of the aquifer have limited the rate of organic matter processing leading to enhanced preservation and storage of the sources such as peats and palaeosols. All groundwater samples are more aromatic for their molecular weight in comparison to lakes and rivers and surface marine samples. The destabilisation or changes in hydrology, whether by anthropogenic or natural processes could lead to the flux of up to ten times more unreacted organic carbon from this coastal aquifer than compared to deeper inland aquifers.


Estuaries ◽  
1994 ◽  
Vol 17 (1) ◽  
pp. 111 ◽  
Author(s):  
Bruce Peterson ◽  
Brian Fry ◽  
Meredith Hullar ◽  
Susan Saupe ◽  
Richard Wright

2011 ◽  
Vol 8 (12) ◽  
pp. 3661-3675 ◽  
Author(s):  
M. I. Stutter ◽  
D. G. Lumsdon ◽  
A. P. Rowland

Abstract. Moorland carbon reserves in organo-mineral soils may be crucial to predicting landscape-scale variability in soil carbon losses, an important component of which is dissolved organic carbon (DOC). Surface water DOC trends are subject to a range of scaling, transport and biotic processes that disconnect them from signals in the catchment's soils. Long-term soil datasets are vital to identify changes in DOC release at source and soil C depletion. Here we show, that moorland soil solution DOC concentrations at three key UK Environmental Change Network sites increased between 1993–2007 in both surface- and sub- soil of a freely-draining Podzol (48 % and 215 % increases in O and Bs horizons, respectively), declined in a gleyed Podzol and showed no change in a Peat. Our principal findings were that: (1) considerable heterogeneity in DOC response appears to exist between different soils that is not apparent from the more consistent observed trends for streamwaters, and (2) freely-draining organo-mineral Podzol showed increasing DOC concentrations, countering the current scientific focus on soil C destabilization in peats. We discuss how the key solubility controls on DOC associated with coupled physico-chemical factors of ionic strength, acid deposition recovery, soil hydrology and temperature cannot readily be separated. Yet, despite evidence that all sites are recovering from acidification the soil-specific responses to environmental change have caused divergence in soil DOC concentration trends. The study shows that the properties of soils govern their specific response to an approximately common set of broad environmental drivers. Key soil properties are indicated to be drainage, sulphate and DOC sorption capacity. Soil properties need representation in process-models to understand and predict the role of soils in catchment to global C budgets. Catchment hydrological (i.e. transport) controls may, at present, be governing the more ubiquitous rises in river DOC concentration trends, but soil (i.e. source) controls provide the key to prediction of future C loss to waters and the atmosphere.


2011 ◽  
Vol 74 (2) ◽  
pp. 133-139 ◽  
Author(s):  
Krzysztof Banaś

The effect of dissolved organic carbon (DOC) on the environmental conditions of macrophytes has been studied in 35 lakes divided into soft- and hardwater: oligohumic (&lt;4.0 mg C dm<sup>-3</sup>), α-mesohumic (4.0-8.0 mg C dm<sup>-3</sup>), β-mesohumic (8.1-16.0 mg C dm<sup>-3</sup>) and polihumic (&gt;16.0 mg C dm<sup>-3</sup>). The optimum environmental conditions for macrophytes have been found in oligohumic lakes, characterised by low water colour and its good transparency. In soft- and hardwater lakes increasing concentration of DOC is accompanied with an increase in the colour (r=0.95), while the visibility decreases. With increasing DOC in the near-sediment layer the pH values decrease while the concentration of nitrogen increases and the concentration of phosphorus slightly increases. In hardwater lakes with increasing DOC concentration, the redox potential, conductivity, total hardness and calcium concentration in the near-sediment water decrease, whereas the content of CO<sup>2</sup> remains at a very low level.


2015 ◽  
Vol 12 (16) ◽  
pp. 13793-13817 ◽  
Author(s):  
Z. T. Yu ◽  
X. J. Wang ◽  
E. L. Zhang ◽  
C. Y. Zhao ◽  
H. Y. Lan

Abstract. Lake sediment is an important carbon reservoir. However, little is known on the dynamics and sources of sediment organic carbon in the Bosten Lake. We collected 13 surface (0–2 cm) sediment samples in the Bosten Lake and analyzed total organic carbon (TOC), total nitrogen (TN), stable carbon isotopic composition in TOC (δ13Corg) and grain size. We found a large spatial variability in TOC content (1.8–4.4 %) and δ13Corg value (−26.77 to −23.98 ‰). Using a three end member mixing model with measured TOC : TN ratio and δ13Corg, we estimated that 54–90 % of TOC was from autochthonous sources. Higher TOC content (> 3.7 %) was found in the east and central-north sections and near the mouth of the Kaidu River, which was attributable to allochthonous, autochthonous plus allochthonous, and autochthonous sources, respectively. The lowest TOC content was found in the mid-west section, which might be a result of high kinetic energy levels. Our study indicated that the spatial distribution of sediment TOC in the Bosten Lake was influenced by multiple and complex processes.


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