scholarly journals Paleoenvironmental Interpretations on Organic Carbon Isotopic Records from Lake Sediments:A Critique

2001 ◽  
Vol 13 (1) ◽  
pp. 72-78 ◽  
Author(s):  
YU Junqing ◽  
◽  
WANG Xiaoy an ◽  
LI Jun ◽  
AN Zhisheng
Keyword(s):  
Organic Carbon ◽  
Carbon Isotopic ◽  
Isotopic Records

Long-term Aptian marine osmium isotopic record of Ontong Java Nui activity

Geology ◽  
2021 ◽  
Author(s):  
Hironao Matsumoto ◽  
Rodolfo Coccioni ◽  
Fabrizio Frontalini ◽  
Kotaro Shirai ◽  
Luigi Jovane ◽  
...  
Keyword(s):  
Organic Carbon ◽  
Volcanic Eruptions ◽  
Hydrothermal Activity ◽  
Published Data ◽  
Isotopic Data ◽  
Oceanic Plateaus ◽  
Carbon Burial ◽  
Organic Carbon Burial ◽  
Isotopic Records

The early to mid-Aptian was punctuated by episodic phases of organic-carbon burial in various oceanographic settings, which are possibly related to massive volcanism associated with the emplacement of the Ontong Java, Manihiki, and Hikurangi oceanic plateaus in the southwestern Pacific Ocean, inferred to have formed a single plateau called Ontong Java Nui. Sedimentary osmium (Os) isotopic compositions are one of the best proxies for determining the timing of voluminous submarine volcanic episodes. However, available Os isotopic records during the age are limited to a narrow interval in the earliest Aptian, which is insufficient for the reconstruction of long-term hydrothermal activity. We document the early to mid-Aptian Os isotopic record using pelagic Tethyan sediments deposited in the Poggio le Guaine (Umbria-Marche Basin, Italy) to precisely constrain the timing of massive volcanic episodes and to assess their impact on the marine environment. Our new Os isotopic data reveal three shifts to unradiogenic values, two of which correspond to black shale horizons in the lower to mid-Aptian, namely the Wezel (herein named) and Fallot Levels. These Os isotopic excursions are ascribed to massive inputs of unradiogenic Os to the ocean through hydrothermal activity. Combining the new Os isotopic record with published data from the lowermost Aptian organic-rich interval in the Gorgo a Cerbara section of the Umbria-Marche Basin, it can be inferred that Ontong Java Nui volcanic eruptions persisted for ~5 m.y. during the early to mid-Aptian.

scholarly journals Spatial distribution and sources of organic carbon in the surface sediment of the Bosten Lake, China

2015 ◽  
Vol 12 (16) ◽  
pp. 13793-13817 ◽  
Author(s):  
Z. T. Yu ◽  
X. J. Wang ◽  
E. L. Zhang ◽  
C. Y. Zhao ◽  
H. Y. Lan
Keyword(s):  
Spatial Distribution ◽  
Organic Carbon ◽  
Energy Levels ◽  
Carbon Isotopic Composition ◽  
Bosten Lake ◽  
Carbon Isotopic ◽  
Complex Processes ◽  
High Kinetic Energy ◽  
Carbon Reservoir ◽  
Kaidu River

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.

scholarly journals Diurnal variations of organic molecular tracers and stable carbon isotopic compositions in atmospheric aerosols over Mt. Tai in North China Plain: an influence of biomass burning

2012 ◽  
Vol 12 (4) ◽  
pp. 9079-9124
Author(s):  
P. Q. Fu ◽  
K. Kawamura ◽  
J. Chen ◽  
J. Li ◽  
Y. L. Sun ◽  
...  
Keyword(s):  
Organic Carbon ◽  
Biomass Burning ◽  
North China Plain ◽  
North China ◽  
Secondary Organic Aerosol ◽  
Organic Aerosol ◽  
Total Carbon ◽  
Stable Carbon ◽  
Isotopic Compositions ◽  
Carbon Isotopic

Abstract. Organic tracer compounds of tropospheric aerosols, as well as organic carbon (OC), elemental carbon (EC), water-soluble organic carbon (WSOC), and stable carbon isotope ratios (δ13C) of total carbon (TC) have been investigated for aerosol samples collected during early and late periods of Mount Tai eXperiment 2006 (MTX2006) field campaign in North China Plain. Total solvent extracts were investigated by gas chromatography/mass spectrometry. More than 130 organic compounds were detected in the aerosol samples. They were grouped into twelve organic compound classes, including biomass burning tracers, biogenic primary sugars, biogenic secondary organic aerosol (SOA) tracers, and anthropogenic tracers such as phthalates, hopanes and polycyclic aromatic hydrocarbons (PAHs). In early June when the field burning activities of wheat straws in North China Plain were very active, the total identified organics (2090 ± 1170 ng m−3) were double those in late June (926 ± 574 ng m−3). All the compound classes were more abundant in early June than in late June, except phthalate esters, which were higher in late June. Levoglucosan (88–1210 ng m−3, 403 ng m−3) was found as the most abundant single compound in early June, while diisobutyl phthalate was the predominant species in late June. During the biomass-burning period in early June, the diurnal trends of most of the primary and secondary organic aerosol tracers were characterized by the concentration peaks observed at mid-night or in early morning, while in late June most of the organic species peaked in late afternoon. This suggests that smoke plumes from biomass burning can uplift the aerosol particulate matter to a certain altitude and then transported to and encountered the summit of Mt. Tai during nighttime. On the basis of the tracer-based method for the estimation of biomass-burning OC, fungal-spore OC and biogenic secondary organic carbon (SOC), we estimate that an average of 24% (up to 64%) of the OC in the Mt. Tai aerosols was due to biomass burning in early June, followed by the contribution of isoprene SOC (mean 4.3%). In contrast, isoprene SOC was the main contributor (6.6%) to OC, and only 3.0% of the OC was due to biomass burning in late June. In early June, δ13C of TC (−26.6‰ to −23.2‰, mean −25.0‰) were lower than those (−23.9‰ to −21.9‰, mean −22.9‰) in late June. In addition, a strong anti-correlation was found between levoglucosan and δ13C values. This study demonstrates that crop-residue burning activities can significantly enhance the organic aerosol loading and alter the organic molecular compositions and stable carbon isotopic compositions of aerosol particles in the troposphere over North China Plain.

scholarly journals Carbon Isotopic Composition of Deep Carbon Gases in an Ombrogenous Peatland, Northwestern Ontario, Canada

Radiocarbon ◽  
1993 ◽  
Vol 35 (2) ◽  
pp. 271-276 ◽  
Author(s):  
Ramon Aravena ◽  
B. G. Warner ◽  
D. J. Charman ◽  
L. R. Belyea ◽  
S. P. Mathur ◽  
...  
Keyword(s):  
Organic Carbon ◽  
Radiocarbon Dating ◽  
Carbon Isotopic Composition ◽  
Downward Movement ◽  
Terrestrial Biosphere ◽  
Carbon Isotopic ◽  
Northwestern Ontario ◽  
Global Carbon ◽  
Isotope Analyses ◽  
Carbon Gases

Radiocarbon dating and carbon isotope analyses of deep peat and gases in a small ombrogenous peatland in northwestern Ontario reveals the presence of old gases at depth that are 1000–2000 yr younger than the enclosing peat. We suggest that the most likely explanation to account for this age discrepancy is the downward movement by advection of younger dissolved organic carbon for use by fermentation and methanogens bacteria. This study identifies a potentially large supply of old carbon gases in peatlands that should be considered in global carbon models of the terrestrial biosphere.

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 ◽  
...  
Keyword(s):  
Organic Carbon ◽  
Dissolved Organic Carbon ◽  
Coastal Aquifer ◽  
Carbon Isotopic Composition ◽  
Median Concentration ◽  
Carbon Isotopic ◽  
Groundwater Samples ◽  
Doc Concentration ◽  
Geochemical Analyses ◽  
Terrestrial Subsurface

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.

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