scholarly journals Spatial variability of organic matter molecular composition and elemental geochemistry in surface sediments of a small boreal Swedish lake

2017 ◽  
Vol 14 (7) ◽  
pp. 1773-1792 ◽  
Author(s):  
Julie Tolu ◽  
Johan Rydberg ◽  
Carsten Meyer-Jacob ◽  
Lorenz Gerber ◽  
Richard Bindler

Abstract. The composition of sediment organic matter (OM) exerts a strong control on biogeochemical processes in lakes, such as those involved in the fate of carbon, nutrients and trace metals. While between-lake spatial variability of OM quality is increasingly investigated, we explored in this study how the molecular composition of sediment OM varies spatially within a single lake and related this variability to physical parameters and elemental geochemistry. Surface sediment samples (0–10 cm) from 42 locations in Härsvatten – a small boreal forest lake with a complex basin morphometry – were analyzed for OM molecular composition using pyrolysis gas chromatography mass spectrometry for the contents of 23 major and trace elements and biogenic silica. We identified 162 organic compounds belonging to different biochemical classes of OM (e.g., carbohydrates, lignin and lipids). Close relationships were found between the spatial patterns of sediment OM molecular composition and elemental geochemistry. Differences in the source types of OM (i.e., terrestrial, aquatic plant and algal) were linked to the individual basin morphometries and chemical status of the lake. The variability in OM molecular composition was further driven by the degradation status of these different source pools, which appeared to be related to sedimentary physicochemical parameters (e.g., redox conditions) and to the molecular structure of the organic compounds. Given the high spatial variation in OM molecular composition within Härsvatten and its close relationship with elemental geochemistry, the potential for large spatial variability across lakes should be considered when studying biogeochemical processes involved in the cycling of carbon, nutrients and trace elements or when assessing lake budgets.

2016 ◽  
Author(s):  
Julie Tolu ◽  
Johan Rydberg ◽  
Carsten Meyer-Jacob ◽  
Lorenz Gerber ◽  
Richard Bindler

Abstract. The composition of organic matter (OM) exerts a strong control on biogeochemical processes in lakes, such as for carbon, nutrients and trace metals. While between-lake spatial variability of OM quality is increasingly investigated, we explored in this study how the molecular composition of sediment OM varies spatially within a single lake, and related this variability to physical parameters and elemental geochemistry. Surface sediment samples (0–10 cm) from 42 locations in Härsvatten – a small, boreal forest lake with a complex basin morphometry – were analyzed for OM molecular composition using pyrolysis-gas chromatography-mass spectrometry, and for the contents of twenty-three major/trace elements and biogenic silica. 160 organic compounds belonging to different biochemical classes (e.g., carbohydrates, lignins, lipids) were identified. Close relationships were found between the spatial patterns of sediment OM molecular composition and elemental geochemistry. Differences in the source types of OM (i.e. terrestrial, aquatic plant and algal OM) were linked to the individual basin morphometries and chemical status of the lake. The variability in OM molecular composition was further driven by the degradation status of these different source-pools, which appeared to be related to sedimentary physico-chemical parameters (e.g., redox conditions) and to the molecular structure of the organic compounds. Given the high spatial variation in OM molecular composition within Härsvatten and its close relationship with elemental geochemistry, the potential for large spatial variability across lakes should be considered when studying biogeochemical processes involved in the cycling of carbon, nutrients and trace elements or when assessing lake budgets.


2016 ◽  
Vol 18 (3) ◽  
pp. 314-322 ◽  
Author(s):  
Xinyue Guo ◽  
Cai Li ◽  
Yang Gao ◽  
Lei Tang ◽  
Meryem Briki ◽  
...  

Organic molecular composition and carbon and nitrogen isotope ratios of PM2.5samples collected in November 2013 were analyzed using gas chromatography/mass spectrometry and isotope ratio mass spectrometry.


Radiocarbon ◽  
2018 ◽  
Vol 61 (1) ◽  
pp. 101-130 ◽  
Author(s):  
Cruz Ferro-Vázquez ◽  
Joeri Kaal ◽  
Francisco Javier Santos Arévalo ◽  
Felipe Criado Boado

AbstractThis paper evaluates the complexities of radiocarbon (14C) dates from soil organic matter (SOM) in archaeological scenarios. The aqueous NaOH-insoluble residual SOM from Neolithic to medieval sites in NW Spain produced consistently older calibrated14C ages than NaOH-extractable SOM. Using pyrolysis-gas chromatography-mass spectrometry (Py-GC-MS) and thermally assisted hydrolysis and methylation (THM-GC-MS), we analyzed the molecular composition of these SOM fractions, aiming to understand the differences in14C ages and to gain insight on SOM dynamics in relation to age fractionation. The molecular composition of the NaOH-extractable SOM, which accounts for roughly two-thirds of total SOM, has a larger proportion of microbial detritus than the NaOH-insoluble SOM. This might suggest that the discrepancies between the two fractions is due to microbial rejuvenation in the extractable fraction, leading to14C results that are younger than the activity that is to be dated. However, archaeological evidence presented here unambiguously shows that the14C age of the extractable SOM provides the more accurate age for the targeted activity, and that the insoluble fraction contains inherited old carbon. After statistical data evaluation using Partial Least Squares-Regression (PLS-R), it is concluded that this inherited SOM is a mixture of Black Carbon from wild and/or domestic fires and recalcitrant aliphatic SOM.


Sign in / Sign up

Export Citation Format

Share Document