scholarly journals Preservation of terrestrial organic carbon in marine sediments off shore Taiwan: mountain building and atmospheric carbon dioxide sequestration

2013 ◽  
Vol 1 (1) ◽  
pp. 177-206
Author(s):  
S.-J. Kao ◽  
R. G. Hilton ◽  
K. Selvaraj ◽  
M. Dai ◽  
F. Zehetner ◽  
...  
Keyword(s):  
Carbon Dioxide ◽  
Organic Carbon ◽  
Marine Sediments ◽  
Atmospheric Carbon Dioxide ◽  
Climatic Variability ◽  
Deep Ocean ◽  
Sediment Traps ◽  
Terrestrial Biosphere ◽  
Atmospheric Carbon ◽  
Carbon Dioxide Co2

Abstract. Geological sequestration of atmospheric carbon dioxide (CO2) can be achieved by the erosion of organic carbon (OC) from the terrestrial biosphere and its burial in long-lived marine sediments. Rivers on mountain islands of Oceania in the western Pacific have very high rates of OC export to the ocean, yet its preservation offshore remains poorly constrained. Here we use the OC content (Corg, %), radiocarbon (Δ14Corg) and stable isotope (δ13Corg) composition of sediments offshore Taiwan to assess the fate of terrestrial OC. We account for rock-derived fossil OC to assess the preservation of OC eroded from the terrestrial biosphere (non-fossil OC) during flood discharges (hyperpycnal river plumes) and when river inputs are dispersed more widely (hypopycnal). The Corg, Δ14Corg and δ13Corg of marine sediment traps and cores indicate that during flood discharges, terrestrial OC is transferred efficiently to the deep ocean and accumulates offshore with little evidence for terrestrial OC loss. In marine sediments fed by dispersive river inputs, the Corg, Δ14Corg and δ13Corg are consistent with mixing of marine OC and terrestrial OC and suggest that efficient preservation of terrestrial OC (> 70%) is also associated with hypopycnal delivery. Re-burial of fossil OC is pervasive. Our findings from Taiwan suggest that erosion and marine burial of terrestrial non-fossil OC may sequester > 8 TgC yr−1 across Oceania, a significant geological CO2 sink which requires better constraint. We postulate that mountain islands of Oceania provide strong link between tectonic uplift and the carbon cycle, one moderated by the climatic variability that controls terrestrial OC delivery to the ocean.

scholarly journals Preservation of terrestrial organic carbon in marine sediments offshore Taiwan: mountain building and atmospheric carbon dioxide sequestration

2014 ◽  
Vol 2 (1) ◽  
pp. 127-139 ◽  
Author(s):  
S.-J. Kao ◽  
R. G. Hilton ◽  
K. Selvaraj ◽  
M. Dai ◽  
F. Zehetner ◽  
...  
Keyword(s):  
Carbon Dioxide ◽  
Organic Carbon ◽  
Marine Sediments ◽  
Atmospheric Carbon Dioxide ◽  
Climatic Variability ◽  
Deep Ocean ◽  
Terrestrial Biosphere ◽  
Holocene Sediments ◽  
Co2 Sink ◽  
Atmospheric Carbon

Abstract. Geological sequestration of atmospheric carbon dioxide (CO2) can be achieved by the erosion of organic carbon (OC) from the terrestrial biosphere and its burial in long-lived marine sediments. Rivers on mountain islands of Oceania in the western Pacific have very high rates of OC export to the ocean, yet its preservation offshore remains poorly constrained. Here we use the OC content (Corg, %), radiocarbon (Δ 14Corg) and stable isotope (δ13Corg) composition of sediments offshore Taiwan to assess the fate of terrestrial OC, using surface, sub-surface and Holocene sediments. We account for rock-derived OC to assess the preservation of OC eroded from the terrestrial biosphere and the associated CO2 sink during flood discharges (hyperpycnal river plumes) and when river inputs are dispersed more widely (hypopycnal). The Corg, Δ14Corg and δ 13Corg of marine sediment traps and cores indicate that during flood discharges, terrestrial OC can be transferred efficiently down submarine canyons to the deep ocean and accumulates offshore with little evidence for terrestrial OC loss. In marine sediments fed by dispersive river inputs, the Corg, Δ14Corg and δ 13Corg are consistent with mixing of terrestrial OC with marine OC and suggest that efficient preservation of terrestrial OC (>70%) is also associated with hypopycnal delivery. Sub-surface and Holocene sediments indicate that this preservation is long-lived on millennial timescales. Re-burial of rock-derived OC is pervasive. Our findings from Taiwan suggest that erosion and offshore burial of OC from the terrestrial biosphere may sequester >8 TgC yr−1 across Oceania, a significant geological CO2 sink which requires better constraint. We postulate that mountain islands of Oceania provide a strong link between tectonic uplift and the carbon cycle, one moderated by the climatic variability which controls terrestrial OC delivery to the ocean.

scholarly journals The Influence of Ocean Thermocline Temperatures on the Earth’s Surface Climate

2005 ◽  
Vol 18 (13) ◽  
pp. 2222-2246 ◽  
Author(s):  
Robert J. Oglesby ◽  
Monica Y. Stephens ◽  
Barry Saltzman
Keyword(s):  
Carbon Dioxide ◽  
Mixed Layer ◽  
General Circulation ◽  
Atmospheric Carbon Dioxide ◽  
Deep Ocean ◽  
High Latitudes ◽  
Surface Climate ◽  
Low Latitudes ◽  
Atmospheric Carbon ◽  
The Impact

Abstract A coupled mixed layer–atmospheric general circulation model has been used to evaluate the impact of ocean thermocline temperatures (and by proxy those of the deep ocean) on the surface climate of the earth. Particular attention has been devoted to temperature regimes both warmer and cooler than at present. The mixed layer ocean model (MLOM) simulates vertical dynamics and thermodynamics in the upper ocean, including wind mixing and buoyancy effects, and has been coupled to the NCAR Community Climate Model (CCM3). Simulations were made with globally uniform thermocline warmings of +2°, +5°, and +10°C, as well as a globally uniform cooling of −5°C. A simulation was made with latitudinally varying changes in thermocline temperature such that the warming at mid- and high latitudes is much larger than at low latitudes. In all simulations, the response of surface temperature over both land and ocean was larger than that expected just as a result of the imposed thermocline temperature change, largely because of water vapor feedbacks. In this respect, the simulations were similar to those in which only changes in atmospheric carbon dioxide were imposed. In fact, when carbon dioxide was explicitly changed along with thermocline temperatures, the results were not much different than if only the thermocline temperatures were altered. Land versus ocean differences are explained largely by latent heat flux differences: the ocean is an infinite evaporative source, while land can be quite dry. The latitudinally varying case has a much larger response at mid- to high latitudes than at low latitudes; the high latitudes actually appear to effectively warm the low latitudes. Simulations exploring scenarios of glacial inception suggest that the deep ocean alone is not likely to be a key trigger but must operate in conjunction with other forcings, such as reduced carbon dioxide. Moist upland regions at mid- and high latitudes, and land regions adjacent to perennial sea ice, are the preferred locations for glacial inception in these runs. Finally, the model combination equilibrates very rapidly, meaning that a large number of simulations can be made for a fairly modest computational cost. A drawback to this is greatly reduced sensitivity to parameters such as atmospheric carbon dioxide, which requires a full response of the ocean. Thus, this approach can be considered intermediate between fixing, or prescribing, sea surface temperatures and a fully coupled modeling approach.

scholarly journals Using airborne HIAPER Pole-to-Pole Observations (HIPPO) to evaluate model and remote sensing estimates of atmospheric carbon dioxide

2016 ◽  
Author(s):  
C. Frankenberg ◽  
S. S. Kulawik ◽  
S. Wofsy ◽  
F. Chevallier ◽  
B. Daube ◽  
...  
Keyword(s):  
Carbon Dioxide ◽  
Atmospheric Carbon Dioxide ◽  
Correlation Coefficients ◽  
Added Value ◽  
Total Carbon ◽  
Accuracy And Precision ◽  
Atmospheric Carbon ◽  
Carbon Dioxide Co2 ◽  
Global Carbon ◽  
Comparable Quality

Abstract. In recent years, space-borne observations of atmospheric carbon-dioxide (CO2) have become increasingly used in global carbon-cycle studies. In order to obtain added value from space-borne measurements, they have to suffice stringent accuracy and precision requirements, with the latter being less crucial as it can be reduced by just enhanced sample size. Validation of CO2 column averaged dry air mole fractions (XCO2) heavily relies on measurements of the Total Carbon Column Observing Network TCCON. Owing to the sparseness of the network and the requirements imposed on space-based measurements, independent additional validation is highly valuable. Here, we use observations from the HIAPER Pole-to-Pole Observations (HIPPO) flights from January 2009 through September 2011 to validate CO2 measurements from satellites (GOSAT, TES, AIRS) and atmospheric inversion models (CarbonTracker CT2013B, MACC v13r1). We find that the atmospheric models capture the XCO2 variability observed in HIPPO flights very well, with correlation coefficients (r2) of 0.93 and 0.95 for CT2013B and MACC, respectively. Some larger discrepancies can be observed in profile comparisons at higher latitudes, esp. at 300 hPa during the peaks of either carbon uptake or release. These deviations can be up to 4 ppm and hint at misrepresentation of vertical transport. Comparisons with the GOSAT satellite are of comparable quality, with an r2 of 0.85, a mean bias μ of −0.06 ppm and a standard deviation σ of 0.45 ppm. TES exhibits an r2 of 0.75, μ of 0.34 ppm and σ of 1.13 ppm. For AIRS, we find an r2 of 0.37, μ of 1.11 ppm and σ of 1.46 ppm, with latitude-dependent biases. For these comparisons at least 6, 20 and 50 atmospheric soundings have been averaged for GOSAT, TES and AIRS, respectively. Overall, we find that GOSAT soundings over the remote pacific ocean mostly meet the stringent accuracy requirements of about 0.5 ppm for space-based CO2 observations.

The rate of dissolution of calcium carbonate from the surface of deep-ocean turbidite sediments

1990 ◽  
Vol 331 (1616) ◽  
pp. 41-49 ◽  
Keyword(s):  
Carbon Dioxide ◽  
Atmospheric Carbon Dioxide ◽  
Bottom Water ◽  
Natural Radionuclide ◽  
Carbon Dioxide Concentration ◽  
Deep Ocean ◽  
Sediment Surface ◽  
Carbonate Sediments ◽  
Sedimentary Record ◽  
Atmospheric Carbon

It is known that past periods of high atmospheric carbon dioxide concentration are associated with poor carbonate preservation in the deep-ocean sedimentary record. Bottom water can become more aggressive towards carbonate sediments during such periods. To interpret the sedimentary record more exactly, and to predict future atmospheric carbon dioxide levels, it is necessary to know the rate of solution of carbonate for a given degree of bottom-water undersaturation. In parts of the Atlantic Ocean, turbidite sedimentation mechanisms have emplaced carbonate-rich material in contact with undersaturated bottom water. The time of the emplacement event can be determined from natural radionuclide distributions, and the degree of carbonate dissolution in this time can be measured. This provides a direct measurement of dissolution rate from a natural sediment surface at a known degree of undersaturation. The range of applicability of the method is explored with a mathematical model, and field data from a 5430 m depth Atlantic site are presented.

scholarly journals Development and field testing of a rapid and ultra-stable atmospheric carbon dioxide spectrometer

2014 ◽  
Vol 7 (8) ◽  
pp. 8101-8123
Author(s):  
B. Xiang ◽  
D. D. Nelson ◽  
J. B. McManus ◽  
M. S. Zahniser ◽  
R. Wehr ◽  
...  
Keyword(s):  
Carbon Dioxide ◽  
Field Test ◽  
Atmospheric Carbon Dioxide ◽  
Field Measurements ◽  
Field Testing ◽  
Thermal Control ◽  
Long Term Ecological Research ◽  
Calibration Protocol ◽  
Atmospheric Carbon ◽  
Carbon Dioxide Co2

Abstract. We present field test results for a new spectroscopic instrument to measure atmospheric carbon dioxide (CO2) with high precision (0.02 ppm at 1 Hz) and demonstrate high stability (within 0.1 ppm over more than 8 months), without the need for hourly, daily, or even monthly calibration against high-pressure gas cylinders. The technical novelty of this instrument (ABsolute Carbon dioxide, ABC) is the spectral null method using an internal quartz reference cell with known CO2 column density. Compared to a previously described prototype, the field instrument has better stability and benefits from more precise thermal control of the optics and more accurate pressure measurements in the sample cell (at the mTorr level). The instrument has been deployed at a long-term ecological research site (the Harvard Forest, USA), where it has measured for eight months without on-site calibration and with minimal maintenance, showing drift bounds of less than 0.1 ppm. Field measurements agree well with those of another commercially available cavity ring-down CO2 instrument (Picarro G2301) run with a standard calibration protocol. This field test demonstrates that ABC is capable of performing high-accuracy, unattended, continuous field measurements with minimal use of calibration cylinders.

Constraining a terrestrial biosphere model with remotely sensed atmospheric carbon dioxide

2017 ◽  
Vol 203 ◽  
pp. 109-124 ◽  
Author(s):  
T. Kaminski ◽  
M. Scholze ◽  
M. Vossbeck ◽  
W. Knorr ◽  
M. Buchwitz ◽  
...  
Keyword(s):  
Carbon Dioxide ◽  
Atmospheric Carbon Dioxide ◽  
Remotely Sensed ◽  
Terrestrial Biosphere ◽  
Atmospheric Carbon ◽  
Biosphere Model

scholarly journals Assessment of recent advances in measurement techniques for atmospheric carbon dioxide and methane observations

2016 ◽  
Vol 9 (9) ◽  
pp. 4737-4757 ◽  
Author(s):  
Christoph Zellweger ◽  
Lukas Emmenegger ◽  
Mohd Firdaus ◽  
Juha Hatakka ◽  
Martin Heimann ◽  
...  
Keyword(s):  
Carbon Dioxide ◽  
Atmospheric Carbon Dioxide ◽  
Measurement Techniques ◽  
Spectroscopic Techniques ◽  
Cavity Output ◽  
The World ◽  
Atmospheric Carbon ◽  
Carbon Dioxide Co2 ◽  
Improved Accuracy ◽  
Flame Ionisation

Abstract. Until recently, atmospheric carbon dioxide (CO2) and methane (CH4) measurements were made almost exclusively using nondispersive infrared (NDIR) absorption and gas chromatography with flame ionisation detection (GC/FID) techniques, respectively. Recently, commercially available instruments based on spectroscopic techniques such as cavity ring-down spectroscopy (CRDS), off-axis integrated cavity output spectroscopy (OA-ICOS) and Fourier transform infrared (FTIR) spectroscopy have become more widely available and affordable. This resulted in a widespread use of these techniques at many measurement stations. This paper is focused on the comparison between a CRDS "travelling instrument" that has been used during performance audits within the Global Atmosphere Watch (GAW) programme of the World Meteorological Organization (WMO) with instruments incorporating other, more traditional techniques for measuring CO2 and CH4 (NDIR and GC/FID). We demonstrate that CRDS instruments and likely other spectroscopic techniques are suitable for WMO/GAW stations and allow a smooth continuation of historic CO2 and CH4 time series. Moreover, the analysis of the audit results indicates that the spectroscopic techniques have a number of advantages over the traditional methods which will lead to the improved accuracy of atmospheric CO2 and CH4 measurements.

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