Tracking natural organic carbon in the River Clyde, UK, using glycerol dialkyl glycerol tetraethers

2017 ◽  
Vol 108 (2-3) ◽  
pp. 289-298 ◽  
Author(s):  
Raquel A. Lopes dos Santos ◽  
Christopher H. Vane
Keyword(s):  
Organic Carbon ◽  
Surface Sediments ◽  
Membrane Lipids ◽  
Stable Carbon Isotope ◽  
Bacterial Membrane ◽  
Stable Carbon ◽  
Outer Estuary ◽  
The Impact ◽  
Marine Archaea ◽  
Glycerol Dialkyl Glycerol Tetraethers

ABSTRACTSurface sediments from a 100-km stretch of the River Clyde, UK, and its estuary were analysed for glycerol dialkyl glycerol tetraethers (GDGTs) to track the downstream changes in the source of organic matter (OM) and to evaluate the impact of urbanisation. Bacterial membrane lipids, named branched GDGTs (brGDGTs), produced in soils and rivers ranged from 1.6 to 58μgg−1 organic carbon (OC) and the isoprenoid GDGT crenarchaeol, mainly from marine archaea, ranged from 0.01 to 42μgg−1 OC. The highest brGDGT concentrations were in the upper river, in Glasgow city and in the outer estuary, suggesting higher soil-derived OM input. By contrast, crenarchaeol concentrations gradually increased from the tidal weir in Glasgow towards the sea. This spatial distribution of the tetraethers was reflected in the branched and isoprenoid tetraether (BIT) index, a proxy for soil versus marine carbon. The highest BIT values (1.0) occurred upstream, estuarine values ranged from 0.9 to 0.6 and the lowest values (0.4) were found in the outer estuary. An independent proxy for soil-derived OM, stable carbon isotope (δ13C) values, showed a comparable decrease in terrigenous OM contribution towards the sea, but was more variable compared to the BIT. Conversely, carbon/nitrogen (C/N) showed a constant trend, suggesting that it is not a reliable indicator of OM source in the Clyde. Neither BIT, δ13C nor C/N were able to reflect the input of urban effluents from Glasgow.

scholarly journals Past climate variations recorded in needle-like aragonites correlate with organic carbon burial efficiency as revealed by lake sediments in Croatia

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Ivan Razum ◽  
Petra Bajo ◽  
Dea Brunović ◽  
Nikolina Ilijanić ◽  
Ozren Hasan ◽  
...  
Keyword(s):  
Organic Carbon ◽  
Stable Carbon Isotope ◽  
Climate Variations ◽  
Before Present ◽  
Stable Carbon ◽  
Climate Trends ◽  
Geochemical Proxies ◽  
Carbon Burial ◽  
Organic Carbon Burial ◽  
Burial Efficiency

AbstractThe drivers of organic carbon (OC) burial efficiency are still poorly understood despite their key role in reliable projections of future climate trends. Here, we provide insights on this issue by presenting a paleoclimate time series of sediments, including the OC contents, from Lake Veliko jezero, Croatia. The Sr/Ca ratios of the bulk sediment are mainly derived from the strontium (Sr) and calcium (Ca) concentrations of needle-like aragonite in Core M1-A and used as paleotemperature and paleohydrology indicators. Four major and six minor cold and dry events were detected in the interval from 8.3 to 2.6 calibrated kilo anno before present (cal ka BP). The combined assessment of Sr/Ca ratios, OC content, carbon/nitrogen (C/N) ratios, stable carbon isotope (δ13C) ratios, and modeled geochemical proxies for paleoredox conditions and aeolian input revealed that cold and dry climate states promoted anoxic conditions in the lake, thereby enhancing organic matter preservation and increasing the OC burial efficiency. Our study shows that the projected future increase in temperature might play an important role in the OC burial efficiency of meromictic lakes.

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

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.

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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