scholarly journals Characterizing the origins of dissolved organic carbon in coastal seawater using stable carbon isotope and light absorption characteristics

2021 ◽  
Vol 18 (5) ◽  
pp. 1793-1801
Author(s):  
Heejun Han ◽  
Jeomshik Hwang ◽  
Guebuem Kim
Keyword(s):  
Organic Carbon ◽  
Dissolved Organic Carbon ◽  
Carbon Isotope ◽  
Stable Carbon Isotope ◽  
The Yellow Sea ◽  
Bacterial Degradation ◽  
Western Coast ◽  
Stable Carbon ◽  
Δ13c Values ◽  
Lower Salinity

Abstract. In order to determine the origins of dissolved organic matter (DOM) occurring in the seawater of Sihwa Lake, we measured the stable carbon isotope ratios of dissolved organic carbon (DOC-δ13C) and the optical properties (absorbance and fluorescence) of DOM in two different seasons (March 2017 and September 2018). Sihwa Lake is enclosed by a dike along the western coast of South Korea, and the water is exchanged with the Yellow Sea twice a day through the sluice gates. The DOC concentrations were generally higher in lower-salinity waters in both periods, and excess of DOC was also observed in 2017 in high-salinity waters. Here, the excess DOC represents any DOC concentrations higher than those in the incoming open-ocean seawater. The excess DOC occurring in the lower-salinity waters originated mainly from marine sediments of tidal flats, based on the DOC-δ13C values (-20.7±1.2 ‰) and good correlations among the DOC, humic-like fluorescent DOM (FDOMH), and NH4+ concentrations. However, the origins of the excess DOC observed in 2017 appear to be from two different sources: one mainly from marine sources such as biological production based on the DOC-δ13C values (−19.1 ‰ to −20.5 ‰) and the other mainly from terrestrial sources by land–seawater interactions based on its depleted DOC-δ13C values (−21.5 ‰ to −27.8 ‰). This terrestrial DOM source observed in 2017 was likely associated with DOM on the reclaimed land, which experienced extended exposure to light and bacterial degradation as indicated by the higher spectral slope ratio (SR) of light absorbance and no concurrent increases in the FDOMH and NH4+ concentrations. Our study demonstrates that the combination of these biogeochemical tools can be a powerful tracer of DOM sources and characteristics in coastal environments.

scholarly journals Characterizing the origin of excess dissolved organic carbon in coastal seawater using stable carbon isotope and light absorption characteristics

2020 ◽  
Author(s):  
Heejun Han ◽  
Jeomshik Hwang ◽  
Guebuem Kim
Keyword(s):  
Organic Carbon ◽  
Dissolved Organic Carbon ◽  
Isotopic Ratio ◽  
Stable Carbon Isotope ◽  
Bacterial Degradation ◽  
Salinity Range ◽  
Stable Carbon ◽  
Reclaimed Land ◽  
Δ13c Values ◽  
Coastal Seawater

Abstract. In order to determine the origins of dissolved organic matter (DOM) occurring in coastal seawater of the Sihwa Lake, South Korea, which is semi-enclosed by a dyke, we measured the stable carbon isotopic ratio of dissolved organic carbon (DOC-δ13C) and optical properties (absorbance and fluorescence) of the DOM in two different seasons (March 2017 and September 2018). The concentrations of DOC were generally higher in lower-salinity waters in both periods, while a significant excess of DOC was observed in 2017 in the same salinity range. The main source of DOC, dependent on salinity, was found to be from marine sediments in the freshwater-seawater mixing zone rather than from terrestrial sources based on the DOC-δ13C values (−20.7±1.2 ‰) and good correlations among DOC, humic-like fluorescent DOM (FDOMH), and NH4+ concentrations. However, the excess DOC observed in 2017 seems to originate from terrestrial sources by direct land-seawater interactions rather than from in-situ biological production, considering the lower DOC-δ13C values (−27.8 ‰ to −22.6 ‰) and higher spectral slope ratio (SR) of light absorbance, without increases in FDOMH and NH4+ concentrations. This terrestrial DOM source could have been exposed to light and bacterial degradation for a long time, resulting in nonfluorescent and low-molecular-weight DOM, as this study area is surrounded by the reclaimed land. Our results suggest that the combination of these biogeochemical tools can be a powerful tracer of coastal DOM sources.

Increase in soil stable carbon isotope ratio relates to loss of organic carbon: results from five long-term bare fallow experiments

Oecologia ◽  
2014 ◽  
Vol 177 (3) ◽  
pp. 811-821 ◽  
Author(s):  
Lorenzo Menichetti ◽  
Sabine Houot ◽  
Folkert van Oort ◽  
Thomas Kätterer ◽  
Bent T. Christensen ◽  
...  
Keyword(s):  
Organic Carbon ◽  
Carbon Isotope ◽  
Isotope Ratio ◽  
Stable Carbon Isotope ◽  
Carbon Isotope Ratio ◽  
Stable Carbon ◽  
Stable Carbon Isotope Ratio ◽  
Bare Fallow

The use of stable carbon isotope trends as a correlation tool: an example from the Surat Basin, Australia

2016 ◽  
Vol 56 (1) ◽  
pp. 355 ◽  
Author(s):  
Astrid Hentschel ◽  
Joan S. Esterle ◽  
Sue Golding
Keyword(s):  
Carbon Isotope ◽  
Turning Point ◽  
Stable Carbon Isotope ◽  
Stable Carbon ◽  
Δ13c Values ◽  
Carbon Isotopic ◽  
Gas Source ◽  
Rapid Reversal ◽  
Allogenic Processes ◽  
Coal Measures

The Surat Basin’s Middle Jurassic Walloon Subgroup is a productive coal seam gas source in Queensland, Australia. The Walloon Subgroup can be subdivided into the Upper and Lower Juandah coal measures, the Tangalooma Sandstone, the Taroom Coal Measures, and the Eurombah/Durabilla Formation, from top to bottom. Correlation across the basin is challenging due to high lateral variability and lack of extensive stratigraphic markers. The Walloon Subgroup is also, in places, incised by the overlying Springbok Sandstone, sometimes interpreted as far down as the Tangalooma Sandstone. New age dates suggest that the Walloon Coal Measures are Oxfordian in age and mark a period of high rates of Corg production and burial, and an intermittent decrease of atmospheric pCO2. The un- or dis-conformable base of the Springbok Sandstone coincides with a turning point of this supposedly global phenomenon. This study uses organic stable carbon isotope trends as a correlation tool within the Surat Basin’s Walloon Subgroup and its overlying Springbok Sandstone. Analysis of a stratigraphic suite of coal samples from several wells across the Surat Basin shows a gradual enrichment in 13C up section from the Taroom to the Lower Juandah Coal Measures, with the most positive δ13C values within the Upper Juandah Coal Measures. Thereafter there is a rapid reversal to more negative δ13C values for coal samples of the Springbok Sandstone. The upward enrichment occurs well before the shift in maceral composition to increased inertinite content in the coals, suggesting more global allogenic processes are controlling the carbon isotopic trend. The consistency of these trends lends a more confident correlation for sub-units within the Walloon Subgroup, and assists in determining the level of incision disconformity of the Springbok Sandstone.

scholarly journals High time-resolved measurement of stable carbon isotope composition in water-soluble organic aerosols: method optimization and a case study during winter haze in East China

2018 ◽  
Author(s):  
Wenqi Zhang ◽  
Yan-Lin Zhang ◽  
Fang Cao ◽  
Yankun Xiang ◽  
Yuanyuan Zhang ◽  
...  
Keyword(s):  
Organic Carbon ◽  
Carbon Isotope ◽  
Isotope Composition ◽  
Stable Carbon Isotope ◽  
Organic Aerosols ◽  
Carbon Isotope Composition ◽  
Water Soluble ◽  
High Time ◽  
Stable Carbon ◽  
Air Mass

Abstract. Water soluble organic carbon (WSOC) is a significant fraction of organic carbon (OC) in atmospheric aerosols. WSOC is of great interest due to its significant effects on atmospheric chemistry, the Earth’s climate and human health. Stable carbon isotope (δ13C) can be used to track the potential sources and investigate atmospheric processes of organic aerosols. In this study, a method of simultaneously measuring the mass concentration and δ13C values of WSOC from aerosol samples is established by coupling the Gas Bench II preparation device with isotopic ratio mass spectrometry. The precision and accuracy of isotope determination is better than 0.17 ‰ and 0.5 ‰, respectively, for samples containing carbon larger than 5 μg. This method is then applied for the high time-resolution aerosol samples during a severe wintertime haze period in Nanjing, East China. WSOC varies between 3–32 μg m−3, whereas δ13C-WSOC ranges from −26.24 ‰ to −23.35 ‰. Three different episodes (e.g., namely the Episode 1, the Episode 2, the Episode 3) are identified in the sampling period, showing a different tendency of δ13C-WSOC with the accumulation process of WSOC aerosols. The increases in both the WSOC mass concentrations and the δ13C-WSOC values in the Episode 1 indicate that WSOC is subject to a substantial photochemical aging during the air mass transport. In the Episode 2, the decline of the δ13C-WSOC is accompanied by the increase in the WSOC mass concentrations, which is associated with regional-transported biomass burning emissions. In the Episode 3, heavier isotope (13C) is exclusively enriched in total carbon (TC) compares to WSOC aerosols. This suggests that water-insoluble carbon may contain 13C-enriched components such as dust carbonate which is supported by the enhanced Ca2+ concentrations and air mass trajectories analysis. The present study provides a novel method to determine stable carbon isotope composition of WSOC and it offers a great potential to better understand the source emission, the atmospheric aging and the secondary production of water soluble organic aerosols.

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