Technical Update: Johnson Space Center system using a solid electrolytic cell in a remote location to measure oxygen fugacities in CO/CO2 controlled-atmosphere furnaces

Science.gov (United States)

Jurewicz, A. J. G.; Williams, R. J.; Le, L.; Wagstaff, J.; Lofgren, G.; Lanier, A.; Carter, W.; Roshko, A.

1993-01-01

Details are given for the design and application of a (one atmosphere) redox-control system. This system differs from that given in NASA Technical Memorandum 58234 in that it uses a single solid-electrolytic cell in a remote location to measure the oxygen fugacities of multiple CO/CO2 controlled-atmosphere furnaces. This remote measurement extends the range of sample-furnace conditions that can be measured using a solid-electrolytic cell, and cuts costs by extending the life of the sensors and by minimizing the number of sensors in use. The system consists of a reference furnace and an exhaust-gas manifold. The reference furnace is designed according to the redox control system of NASA Technical Memorandum 58234, and any number of CO/CO2 controlled-atmosphere furnaces can be attached to the exhaust-gas manifold. Using the manifold, the exhaust gas from individual CO/CO2 controlled atmosphere furnaces can be diverted through the reference furnace, where a solid-electrolyte cell is used to read the ambient oxygen fugacity. The oxygen fugacity measured in the reference furnace can then be used to calculate the oxygen fugacity in the individual CO/CO2 controlled-atmosphere furnace. A BASIC computer program was developed to expedite this calculation.

Atmospheric CO2 Variability Observed From ASCENDS Flight Campaigns

Science.gov (United States)

Lin, Bing; Browell, Edward; Campbell, Joel; Choi, Yonghoon; Dobler, Jeremy; Fan, Tai-Fang; Harrison, F. Wallace; Kooi, Susan; Liu, Zhaoyan; Meadows, Byron;

Reconsideration of atmospheric CO2 lifetime: potential mechanism for explaining CO2 missing sink

Science.gov (United States)

Kikuchi, R.; Gorbacheva, T.; Gerardo, R.

2009-04-01

Carbon cycle data (Intergovernmental Panel on Climate Change 1996) indicate that fossil fuel use accounts for emissions to the atmosphere of 5.5±0.5 GtC (Gigatons of carbon) annually. Other important processes in the global CO2 budget are tropical deforestation, estimated to generate about 1.6±1.0 GtC/yr; absorption by the oceans, removing about 2.0±0.8 GtC/yr; and regrowth of northern forests, taking up about 0.5±0.5 GtC/yr. However, accurate measurements of CO2 show that the atmosphere is accumulating only about 3.3±0.2 GtC/yr. The imbalance of about 1.3±1.5 GtC/yr, termed the "missing sink", represents the difference between the estimated sources and the estimated sinks of CO2; that is, we do not know where all of the anthropogenic CO2 is going. Several potential mechanisms have been proposed to explain this missing carbon, such as CO2 fertilization, climate change, nitrogen deposition, land use change, forest regrowth et al. Considering the complexity of ecosystem, most of ecosystem model cannot handle all the potential mechanisms to reproduce the real world. It has been believed that the dominant sink mechanism is the fertilizing effects of increased CO2 concentrations in the atmosphere and the addition to soils of fixed nitrogen from fossil-fuel burning and agricultural fertilizers. However, a recent analysis of long-term observations of the change in biomass and growth rates suggests that such fertilization effects are much too small to explain more than a small fraction of the observed sink. In addition, long-term experiments in which small forest patches and other land ecosystems have been exposed to elevated CO2 levels for extended periods show a rapid decrease of the fertilization effect after an initial enhancement. We will explore this question of the missing sink in atmospheric CO2 residence time. Radioactive and stable carbon isotopes (13-C/12-C) show the real CO2 lifetime is about 5 years; i.e. CO2 is quickly taken out of the atmospheric

A single gas chromatograph for accurate atmospheric mixing ratio measurements of CO2, CH4, N2O, SF6 and CO

Directory of Open Access Journals (Sweden)

H. A. J. Meijer

2009-09-01

Full Text Available We present an adapted gas chromatograph capable of measuring simultaneously and semi-continuously the atmospheric mixing ratios of the greenhouse gases CO2, CH4, N2O and SF6 and the trace gas CO with high precision and long-term stability. The novelty of our design is that all species are measured with only one device, making it a very cost-efficient system. No time lags are introduced between the measured mixing ratios. The system is designed to operate fully autonomously which makes it ideal for measurements at remote and unmanned stations. Only a small amount of sample air is needed, which makes this system also highly suitable for flask air measurements. In principle, only two reference cylinders are needed for daily operation and only one calibration per year against international WMO standards is sufficient to obtain high measurement precision and accuracy. The system described in this paper is in use since May 2006 at our atmospheric measurement site Lutjewad near Groningen, The Netherlands at 6°21´ E, 53°24´N, 1 m a.s.l. Results show the long-term stability of the system. Observed measurement precisions at our remote research station Lutjewad were: ±0.04 ppm for CO2, ±0.8 ppb for CH4, ±0.8 ppb for CO, ±0.3 ppb for N2O, and ±0.1 ppt for SF6. The ambient mixing ratios of all measured species as observed at station Lutjewad for the period of May 2007 to August 2008 are presented as well.

1.6 μm DIAL Measurement and Back Trajectory Analysis of CO2 Concentration Profiles in the Lower-Atmosphere

Science.gov (United States)

Shibata, Y.; Nagasawa, C.; Abo, M.

2016-12-01

Carbon dioxide (CO2) is the primary greenhouse gas emitted through human activities. In addition to the ground level CO2 network, vertical CO2 concentration profiles also play an important role for the estimation of the carbon budget and global warming in the inversion method. Especially, for the detailed analysis of forest carbon dynamics and CO2 fluxes of urban area, vertical CO2 concentration profiles with high spatial and temporal resolution in the lower atmosphere have been conducted by a differential absorption lidar (DIAL). We have observed several vertical profiles of CO2 concentrations for nighttime and daytime from 0.25 to 2.5 km altitude with range resolution of 300 m and integration time of 1 hour. In order to extract information on the origin of the CO2 masses, one day back trajectories were calculated by using a three dimensional (3-D) atmospheric transport model. In many cases, CO2 low concentration layers of over 1.5km altitude were flown by westerly winds from the forest. In another case, high concentration layers of CO2 were flown from the urban areas. As the spectra of absorption lines of any molecules are influenced basically by the temperature in the atmosphere, laser beams of three wavelengths around a CO2 absorption spectrum are transmitted alternately to the atmosphere for simultaneous measurements of CO2 concentration and temperature profiles. Moreover, a few processing algorithms of CO2-DIAL are also performed for improvement of measurement accuracy. For computation of trajectories and drawing their figures, the JRA-25 data provided by the cooperative research project for the JRA-25 long-term reanalysis of the Japan Meteorological Agency (JMA) and the Central Research Institute of Electric Power Industry (CRIEPI) and the NIPR trajectory model (Tomikawa and Sato, 2005; http://firp-nitram.nipr.ac.jp) were used. This work was financially supported by the System Development Program for Advanced Measurement and Analysis of the Japan Science and

Net uptake of atmospheric CO2 by coastal submerged aquatic vegetation

Science.gov (United States)

Tokoro, Tatsuki; Hosokawa, Shinya; Miyoshi, Eiichi; Tada, Kazufumi; Watanabe, Kenta; Montani, Shigeru; Kayanne, Hajime; Kuwae, Tomohiro

2014-01-01

‘Blue Carbon’, which is carbon captured by marine living organisms, has recently been highlighted as a new option for climate change mitigation initiatives. In particular, coastal ecosystems have been recognized as significant carbon stocks because of their high burial rates and long-term sequestration of carbon. However, the direct contribution of Blue Carbon to the uptake of atmospheric CO2 through air-sea gas exchange remains unclear. We performed in situ measurements of carbon flows, including air-sea CO2 fluxes, dissolved inorganic carbon changes, net ecosystem production, and carbon burial rates in the boreal (Furen), temperate (Kurihama), and subtropical (Fukido) seagrass meadows of Japan from 2010 to 2013. In particular, the air-sea CO2 flux was measured using three methods: the bulk formula method, the floating chamber method, and the eddy covariance method. Our empirical results show that submerged autotrophic vegetation in shallow coastal waters can be functionally a sink for atmospheric CO2. This finding is contrary to the conventional perception that most near-shore ecosystems are sources of atmospheric CO2. The key factor determining whether or not coastal ecosystems directly decrease the concentration of atmospheric CO2 may be net ecosystem production. This study thus identifies a new ecosystem function of coastal vegetated systems; they are direct sinks of atmospheric CO2. PMID:24623530

N2O and CO production by electric discharge - Atmospheric implications. [Venus atmosphere simulation

Science.gov (United States)

Levine, J. S.; Howell, W. E.; Hughes, R. E.; Chameides, W. L.

1979-01-01

Enhanced levels of N2O and CO were measured in tropospheric air samples exposed to a 17,500-J laboratory discharge. These enhanced levels correspond to an N2O production rate of about 4 trillion molecules/J and a CO production rate of about 10 to the 14th molecules/J. The CO measurements suggest that the primary region of chemical production in the discharge is the shocked air surrounding the lightning channel, as opposed to the slower-cooling inner core. Additional experiments in a simulated Venus atmosphere (CO2 - 95%, N2 - 5%, at one atmosphere) indicate an enhancement of CO from less than 0.1 ppm prior to the laboratory discharge to more than 2000 ppm after the discharge. Comparison with theoretical calculations appears to confirm the ability of a shock-wave/thermochemical model to predict the rate of production of trace species by an electrical discharge.

Measurements of Atmospheric CO2 Column in Cloudy Weather Conditions using An IM-CW Lidar at 1.57 Micron

Science.gov (United States)

Lin, Bing; Obland, Michael; Harrison, F. Wallace; Nehrir, Amin; Browell, Edward; Campbell, Joel; Dobler, Jeremy; Meadows, Bryon; Fan, Tai-Fang; Kooi, Susan;

South African carbon observations: CO2 measurements for land, atmosphere and ocean

CSIR Research Space (South Africa)

Feig, Gregor T

2017-11-01

Full Text Available , Mudau AE, Monteiro PMS. South African carbon observations: CO2 measurements for land, atmosphere and ocean. S Afr J Sci. 2017;113(11/12), Art. #a0237, 4 pages. http://dx.doi. org/10.17159/sajs.2017/a0237 Carbon dioxide plays a central role in earth... References 1. Houghton RA. Balancing the global carbon budget. Annu Rev Earth Planet Sci. 2007;35:313–347. https://doi.org/10.1146/annurev. earth.35.031306.140057 2. Denman KL. Climate change, ocean processes and ocean iron fertilization. Mar Ecol Prog Ser...

Airborne Lidar for Simultaneous Measurement of Column CO2 and Water Vapor in the Atmosphere

Science.gov (United States)

Singh, Upendra N.; Petros, Mulugeta; Refaat, Tamer F.; Antill, Charles W.; Remus, Ruben; Yu, Jirong

2016-01-01

The 2-micron wavelength region is suitable for atmospheric carbon dioxide (CO2) measurements due to the existence of distinct absorption feathers for the gas at this particular wavelength. For more than 20 years, researchers at NASA Langley Research Center (LaRC) have developed several high-energy and high repetition rate 2-micron pulsed lasers. This paper will provide status and details of an airborne 2-micron triple-pulse integrated path differential absorption (IPDA) lidar. The development of this active optical remote sensing IPDA instrument is targeted for measuring both CO2 and water vapor (H2O) in the atmosphere from an airborne platform. This presentation will focus on the advancement of the 2-micron triple-pulse IPDA lidar development. Updates on the state-of-the-art triple-pulse laser transmitter will be presented including the status of seed laser locking, wavelength control, receiver telescope, detection system and data acquisition. Future plans for the IPDA lidar system for ground integration, testing and flight validation will also be presented.

Thermal infrared laser heterodyne spectroradiometry for solar occultation atmospheric CO2 measurements

Science.gov (United States)

Hoffmann, Alex; Macleod, Neil A.; Huebner, Marko; Weidmann, Damien

2016-12-01

This technology demonstration paper reports on the development, demonstration, performance assessment, and initial data analysis of a benchtop prototype quantum cascade laser heterodyne spectroradiometer, operating within a narrow spectral window of ˜ 1 cm-1 around 953.1 cm-1 in transmission mode and coupled to a passive Sun tracker. The instrument has been specifically designed for accurate dry air total column, and potentially vertical profile, measurements of CO2. Data from over 8 months of operation in 2015 near Didcot, UK, confirm that atmospheric measurements with noise levels down to 4 times the shot noise limit can be achieved with the current instrument. Over the 8-month period, spectra with spectral resolutions of 60 MHz (0.002 cm-1) and 600 MHz (0.02 cm-1) have been acquired with median signal-to-noise ratios of 113 and 257, respectively, and a wavenumber calibration uncertainty of 0.0024 cm-1.Using the optimal estimation method and RFM as the radiative transfer forward model, prior analysis and theoretical benchmark modelling had been performed with an observation system simulator (OSS) to target an optimized spectral region of interest. The selected narrow spectral window includes both CO2 and H2O ro-vibrational transition lines to enable the measurement of dry air CO2 column from a single spectrum. The OSS and preliminary retrieval results yield roughly 8 degrees of freedom for signal (over the entire state vector) for an arbitrarily chosen a priori state with relatively high uncertainty ( ˜ 4 for CO2). Preliminary total column mixing ratios obtained are consistent with GOSAT monthly data. At a spectral resolution of 60 MHz with an acquisition time of 90 s, instrumental noise propagation yields an error of around 1.5 ppm on the dry air total column of CO2, exclusive of biases and geophysical parameters errors at this stage.

Atmospheric CO2 Column Measurements with an Airborne Intensity-Modulated Continuous-Wave 1.57-micron Fiber Laser Lidar

Science.gov (United States)

Dobler, Jeremy T.; Harrison, F. Wallace; Browell, Edward V.; Lin, Bing; McGregor, Doug; Kooi, Susan; Choi, Yonghoon; Ismail, Syed

2013-01-01

The 2007 National Research Council (NRC) Decadal Survey on Earth Science and Applications from Space recommended Active Sensing of CO2 Emissions over Nights, Days, and Seasons (ASCENDS) as a mid-term, Tier II, NASA space mission. ITT Exelis, formerly ITT Corp., and NASA Langley Research Center have been working together since 2004 to develop and demonstrate a prototype Laser Absorption Spectrometer for making high-precision, column CO2 mixing ratio measurements needed for the ASCENDS mission. This instrument, called the Multifunctional Fiber Laser Lidar (MFLL), operates in an intensity-modulated, continuous-wave mode in the 1.57- micron CO2 absorption band. Flight experiments have been conducted with the MFLL on a Lear-25, UC-12, and DC-8 aircraft over a variety of different surfaces and under a wide range of atmospheric conditions. Very high-precision CO2 column measurements resulting from high signal-to-noise (great than 1300) column optical depth measurements for a 10-s (approximately 1 km) averaging interval have been achieved. In situ measurements of atmospheric CO2 profiles were used to derive the expected CO2 column values, and when compared to the MFLL measurements over desert and vegetated surfaces, the MFLL measurements were found to agree with the in situ-derived CO2 columns to within an average of 0.17% or approximately 0.65 ppmv with a standard deviation of 0.44% or approximately 1.7 ppmv. Initial results demonstrating ranging capability using a swept modulation technique are also presented.

Atmospheric inversion of the surface CO2 flux with 13CO2 constraint

Science.gov (United States)

Chen, J. M.; Mo, G.; Deng, F.

2013-10-01

Observations of 13CO2 at 73 sites compiled in the GLOBALVIEW database are used for an additional constraint in a global atmospheric inversion of the surface CO2 flux using CO2 observations at 210 sites for the 2002-2004 period for 39 land regions and 11 ocean regions. This constraint is implemented using the 13CO2/CO2 flux ratio modeled with a terrestrial ecosystem model and an ocean model. These models simulate 13CO2 discrimination rates of terrestrial photosynthesis and respiration and ocean-atmosphere diffusion processes. In both models, the 13CO2 disequilibrium between fluxes to and from the atmosphere is considered due to the historical change in atmospheric 13CO2 concentration. For the 2002-2004 period, the 13CO2 constraint on the inversion increases the total land carbon sink from 3.40 to 3.70 Pg C yr-1 and decreases the total oceanic carbon sink from 1.48 to 1.12 Pg C yr-1. The largest changes occur in tropical areas: a considerable decrease in the carbon source in the Amazon forest, and this decrease is mostly compensated by increases in the ocean region immediately west of the Amazon and the southeast Asian land region. Our further investigation through different treatments of the 13CO2/CO2 flux ratio used in the inversion suggests that variable spatial distributions of the 13CO2 isotopic discrimination rate simulated by the models over land and ocean have considerable impacts on the spatial distribution of the inverted CO2 flux over land and the inversion results are not sensitive to errors in the estimated disequilibria over land and ocean.

A Broad Bank Lidar for Precise Atmospheric CO2 Column Absorption Measurement from Space

Science.gov (United States)

Georgieva, E. M.; Heaps, W. S.; Huang, W.

2010-01-01

Accurate global measurement of carbon dioxide column with the aim of discovering and quantifying unknown sources and sinks has been a high priority for the last decade. In order to uncover the "missing sink" that is responsible for the large discrepancies in the budget the critical precision for a measurement from space needs to be on the order of 1 ppm. To better understand the CO2 budget and to evaluate its impact on global warming the National Research Council (NRC) in its recent decadal survey report (NACP) to NASA recommended a laser based total CO2 mapping mission in the near future. That's the goal of Active Sensing of CO2 Emissions over Nights, Days, and Seasons (ASCENDS) mission - to significantly enhance the understanding of the role of CO2 in the global carbon cycle. Our current goal is to develop an ultra precise, inexpensive new lidar system for column measurements of CO2 changes in the lower atmosphere that uses a Fabry-Perot interferometer based system as the detector portion of the instrument and replaces the narrow band laser commonly used in lidars with a high power broadband source. This approach reduces the number of individual lasers used in the system and considerably reduces the risk of failure. It also tremendously reduces the requirement for wavelength stability in the source putting this responsibility instead on the Fabry- Perot subsystem.

A Ground-based validation of GOSAT-observed atmospheric CO2 in Inner-Mongolian grasslands

International Nuclear Information System (INIS)

Qin, X; Lei, L; Zeng, Z; Kawasaki, M; Oohasi, M

2014-01-01

Atmospheric carbon dioxide (CO 2 ) is a long-lived greenhouse gas that significantly contributes to global warming. Long-term and continuous measurements of atmospheric CO 2 to investigate its global distribution and concentration variations are important for accurately understanding its potential climatic effects. Satellite measurements from space can offer atmospheric CO 2 data for climate change research. For that, ground-based measurements are required for validation and improving the precision of satellite-measured CO 2 . We implemented observation experiment of CO 2 column densities in the Xilinguole grasslands in Inner Mongolia, China, using a ground-based measurement system, which mainly consists of an optical spectrum analyzer (OSA), a sun tracker and a notebook controller. Measurements from our ground-based system were analyzed and compared with those from the Greenhouse gas Observation SATellite (GOSAT). The ground-based measurements had an average value of 389.46 ppm, which was 2.4 ppm larger than from GOSAT, with a standard deviation of 3.4 ppm. This result is slightly larger than the difference between GOSAT and the Total Carbon Column Observing Network (TCCON). This study highlights the usefulness of the ground-based OSA measurement system for analyzing atmospheric CO 2 column densities, which is expected to supplement the current TCCON network

South African integrated carbon observation network (SA-ICON): CO2 measurements on land, atmosphere and ocean

CSIR Research Space (South Africa)

Feig, Gregor T

2016-10-01

Full Text Available It has become essential to accurately estimate the emission and uptake of atmospheric carbon dioxide (CO(sub2)) around the globe. Atmospheric CO(sub2) plays a central role in the Earth’s atmospheric, ocean and terrestrial systems and it has been...

Mesoscale modelling of atmospheric CO2 across Denmark

DEFF Research Database (Denmark)

Lansø, Anne Sofie

2016-01-01

of the simulated atmospheric CO2 across Denmark was, in particular, affected by the Danish terrestrial surface exchanges and its temporal variability. This study urges all future modelling studies of air–sea CO2 to include short-term variability in pCO2. To capture the full heterogeneity of the surface exchanges......It is scientifically well-established that the increase of atmospheric CO2 affects the entire globe and will lead to higher surface temperatures. Although anthropogenic CO2is emitted straight into the atmosphere, it does not all contribute to the existing atmospheric CO2 reservoir. Approximately 29......% is taken up by the global oceans, due to under-saturation of CO2 in the surface waters, while another 33 % is taken up by the terrestrial biosphere, via photosynthesis. In order to estimate the effects of increasing anthropogenic emissions of CO2 more accurately in the future, it is essential to understand...

Temporal variations of atmospheric CO2 and CO at Ahmedabad in western India

Science.gov (United States)

Chandra, Naveen; Lal, Shyam; Venkataramani, S.; Patra, Prabir K.; Sheel, Varun

2016-05-01

About 70 % of the anthropogenic carbon dioxide (CO2) is emitted from the megacities and urban areas of the world. In order to draw effective emission mitigation policies for combating future climate change as well as independently validating the emission inventories for constraining their large range of uncertainties, especially over major metropolitan areas of developing countries, there is an urgent need for greenhouse gas measurements over representative urban regions. India is a fast developing country, where fossil fuel emissions have increased dramatically in the last three decades and are predicted to continue to grow further by at least 6 % per year through to 2025. The CO2 measurements over urban regions in India are lacking. To overcome this limitation, simultaneous measurements of CO2 and carbon monoxide (CO) have been made at Ahmedabad, a major urban site in western India, using a state-of-the-art laser-based cavity ring down spectroscopy technique from November 2013 to May 2015. These measurements enable us to understand the diurnal and seasonal variations in atmospheric CO2 with respect to its sources (both anthropogenic and biospheric) and biospheric sinks. The observed annual average concentrations of CO2 and CO are 413.0 ± 13.7 and 0.50 ± 0.37 ppm respectively. Both CO2 and CO show strong seasonality with lower concentrations (400.3 ± 6.8 and 0.19 ± 0.13 ppm) during the south-west monsoon and higher concentrations (419.6 ± 22.8 and 0.72 ± 0.68 ppm) during the autumn (SON) season. Strong diurnal variations are also observed for both the species. The common factors for the diurnal cycles of CO2 and CO are vertical mixing and rush hour traffic, while the influence of biospheric fluxes is also seen in the CO2 diurnal cycle. Using CO and CO2 covariation, we differentiate the anthropogenic and biospheric components of CO2 and found significant contributions of biospheric respiration and anthropogenic emissions in the late night (00:00-05:00 h, IST

Effects of tillage practice and atmospheric CO2 level on soil CO2 efflux

Science.gov (United States)

Elevated atmospheric carbon dioxide (CO2) affects both the quantity and quality of plant tissues, which impacts the cycling and storage of carbon (C) within plant/soil systems and thus the rate of CO2 release back to the atmosphere. Research to accurately quantify the effects of elevated CO2 and as...

Response of atmospheric CO2 to changes in land use

International Nuclear Information System (INIS)

King, A.W.; Emanuel, W.R.; Post, W.M.

1991-01-01

This chapter examines how different histories of CO 2 release from past changes in land use influence the simulation of past and future changes in atmospheric CO 2 . The authors first simulate past change in atmospheric CO 2 using reconstructed histories of land-use CO 2 release from a historical-ecological model of land-use change and CO 2 release. They examine the impact of each history on the coincidence between simulated and observed atmospheric CO 2 . They then compare these CO 2 release histories, and their contribution to coincidence or noncoincidence of simulation and observation, with histories reconstructed by deconvolution of the atmospheric CO 2 record. They conclude by exploring the implications of these deconvolved reconstructions for the simulation of future changes in atmospheric CO 2

Modeling of intensity-modulated continuous-wave laser absorption spectrometer systems for atmospheric CO(2) column measurements.

Science.gov (United States)

Lin, Bing; Ismail, Syed; Wallace Harrison, F; Browell, Edward V; Nehrir, Amin R; Dobler, Jeremy; Moore, Berrien; Refaat, Tamer; Kooi, Susan A

2013-10-10

The focus of this study is to model and validate the performance of intensity-modulated continuous-wave (IM-CW) CO(2) laser absorption spectrometer (LAS) systems and their CO(2) column measurements from airborne and satellite platforms. The model accounts for all fundamental physics of the instruments and their related CO(2) measurement environments, and the modeling results are presented statistically from simulation ensembles that include noise sources and uncertainties related to the LAS instruments and the measurement environments. The characteristics of simulated LAS systems are based on existing technologies and their implementation in existing systems. The modeled instruments are specifically assumed to be IM-CW LAS systems such as the Exelis' airborne multifunctional fiber laser lidar (MFLL) operating in the 1.57 μm CO(2) absorption band. Atmospheric effects due to variations in CO(2), solar radiation, and thin clouds, are also included in the model. Model results are shown to agree well with LAS atmospheric CO(2) measurement performance. For example, the relative bias errors of both MFLL simulated and measured CO(2) differential optical depths were found to agree to within a few tenths of a percent when compared to the in situ observations from the flight of 3 August 2011 over Railroad Valley (RRV), Nevada, during the summer 2011 flight campaign. In addition, the horizontal variations in the model CO(2) differential optical depths were also found to be consistent with those from MFLL measurements. In general, the modeled and measured signal-to-noise ratios (SNRs) of the CO(2) column differential optical depths (τd) agreed to within about 30%. Model simulations of a spaceborne IM-CW LAS system in a 390 km dawn/dusk orbit for CO(2) column measurements showed that with a total of 42 W of transmitted power for one offline and two different sideline channels (placed at different locations on the side of the CO(2) absorption line), the accuracy of the �

Sugarcane vinasse CO2 gasification and release of ash-forming matters in CO2 and N2 atmospheres.

Science.gov (United States)

Dirbeba, Meheretu Jaleta; Brink, Anders; DeMartini, Nikolai; Lindberg, Daniel; Hupa, Mikko

2016-10-01

Gasification of sugarcane vinasse in CO2 and the release of ash-forming matters in CO2 and N2 atmospheres were investigated using a differential scanning calorimetry and thermogravimetric analyzer (DSC-TGA) at temperatures between 600 and 800°C. The results showed that pyrolysis is the main mechanism for the release of the organics from vinasse. Release of ash-forming matters in the vinasse is the main cause for vinasse char weight losses in the TGA above 700°C. The losses are higher in N2 than in CO2, and increase considerably with temperature. CO2 gasification also consumes the carbon in the vinasse chars while suppressing alkali release. Alkali release was also significant due to volatilization of KCl and reduction of alkali sulfate and carbonate by carbon. The DSC measured thermal events during heating up in N2 atmosphere that correspond to predicted melting temperatures of alkali salts in the char. Copyright © 2016 Elsevier Ltd. All rights reserved.

A role for atmospheric CO2 in preindustrial climate forcing

NARCIS (Netherlands)

Hoof, T.B. van; Wagner-Cremer, F.; Kürschner, W.M.; Visscher, H.

2008-01-01

Complementary to measurements in Antarctic ice cores, stomatal frequency analysis of leaves of land plants preserved in peat and lake deposits can provide a proxy record of preindustrial atmospheric CO2 concentration. CO2 trends based on leaf remains of Quercus robur (English oak) from the

A Pilot Study to Evaluate California's Fossil Fuel CO2 Emissions Using Atmospheric Observations

Science.gov (United States)

Graven, H. D.; Fischer, M. L.; Lueker, T.; Guilderson, T.; Brophy, K. J.; Keeling, R. F.; Arnold, T.; Bambha, R.; Callahan, W.; Campbell, J. E.; Cui, X.; Frankenberg, C.; Hsu, Y.; Iraci, L. T.; Jeong, S.; Kim, J.; LaFranchi, B. W.; Lehman, S.; Manning, A.; Michelsen, H. A.; Miller, J. B.; Newman, S.; Paplawsky, B.; Parazoo, N.; Sloop, C.; Walker, S.; Whelan, M.; Wunch, D.

2016-12-01

Atmospheric CO2 concentration is influenced by human activities and by natural exchanges. Studies of CO2 fluxes using atmospheric CO2 measurements typically focus on natural exchanges and assume that CO2 emissions by fossil fuel combustion and cement production are well-known from inventory estimates. However, atmospheric observation-based or "top-down" studies could potentially provide independent methods for evaluating fossil fuel CO2 emissions, in support of policies to reduce greenhouse gas emissions and mitigate climate change. Observation-based estimates of fossil fuel-derived CO2 may also improve estimates of biospheric CO2 exchange, which could help to characterize carbon storage and climate change mitigation by terrestrial ecosystems. We have been developing a top-down framework for estimating fossil fuel CO2 emissions in California that uses atmospheric observations and modeling. California is implementing the "Global Warming Solutions Act of 2006" to reduce total greenhouse gas emissions to 1990 levels by 2020, and it has a diverse array of ecosystems that may serve as CO2 sources or sinks. We performed three month-long field campaigns in different seasons in 2014-15 to collect flask samples from a state-wide network of 10 towers. Using measurements of radiocarbon in CO2, we estimate the fossil fuel-derived CO2 present in the flask samples, relative to marine background air observed at coastal sites. Radiocarbon (14C) is not present in fossil fuel-derived CO2 because of radioactive decay over millions of years, so fossil fuel emissions cause a measurable decrease in the 14C/C ratio in atmospheric CO2. We compare the observations of fossil fuel-derived CO2 to simulations based on atmospheric modeling and published fossil fuel flux estimates, and adjust the fossil fuel flux estimates in a statistical inversion that takes account of several uncertainties. We will present the results of the top-down technique to estimate fossil fuel emissions for our field

Temporal variations of atmospheric CO2 and CO at Ahmedabad in western India

Directory of Open Access Journals (Sweden)

N. Chandra

2016-05-01

Full Text Available About 70 % of the anthropogenic carbon dioxide (CO2 is emitted from the megacities and urban areas of the world. In order to draw effective emission mitigation policies for combating future climate change as well as independently validating the emission inventories for constraining their large range of uncertainties, especially over major metropolitan areas of developing countries, there is an urgent need for greenhouse gas measurements over representative urban regions. India is a fast developing country, where fossil fuel emissions have increased dramatically in the last three decades and are predicted to continue to grow further by at least 6 % per year through to 2025. The CO2 measurements over urban regions in India are lacking. To overcome this limitation, simultaneous measurements of CO2 and carbon monoxide (CO have been made at Ahmedabad, a major urban site in western India, using a state-of-the-art laser-based cavity ring down spectroscopy technique from November 2013 to May 2015. These measurements enable us to understand the diurnal and seasonal variations in atmospheric CO2 with respect to its sources (both anthropogenic and biospheric and biospheric sinks. The observed annual average concentrations of CO2 and CO are 413.0 ± 13.7 and 0.50 ± 0.37 ppm respectively. Both CO2 and CO show strong seasonality with lower concentrations (400.3 ± 6.8 and 0.19 ± 0.13 ppm during the south-west monsoon and higher concentrations (419.6 ± 22.8 and 0.72 ± 0.68 ppm during the autumn (SON season. Strong diurnal variations are also observed for both the species. The common factors for the diurnal cycles of CO2 and CO are vertical mixing and rush hour traffic, while the influence of biospheric fluxes is also seen in the CO2 diurnal cycle. Using CO and CO2 covariation, we differentiate the anthropogenic and biospheric components of CO2 and found significant contributions of biospheric respiration and anthropogenic

Carbon balance of China constrained by CONTRAIL aircraft CO2 measurements

Science.gov (United States)

Jiang, F.; Wang, H. M.; Chen, J. M.; Machida, T.; Zhou, L. X.; Ju, W. M.; Matsueda, H.; Sawa, Y.

2014-09-01

Terrestrial carbon dioxide (CO2) flux estimates in China using atmospheric inversion method are beset with considerable uncertainties because very few atmospheric CO2 concentration measurements are available. In order to improve these estimates, nested atmospheric CO2 inversion during 2002-2008 is performed in this study using passenger aircraft-based CO2 measurements over Eurasia from the Comprehensive Observation Network for Trace gases by Airliner (CONTRAIL) project. The inversion system includes 43 regions with a focus on China, and is based on the Bayesian synthesis approach and the TM5 transport model. The terrestrial ecosystem carbon flux modeled by the Boreal Ecosystems Productivity Simulator (BEPS) model and the ocean exchange simulated by the OPA-PISCES-T model are considered as the prior fluxes. The impacts of CONTRAIL CO2 data on inverted China terrestrial carbon fluxes are quantified, the improvement of the inverted fluxes after adding CONTRAIL CO2 data are rationed against climate factors and evaluated by comparing the simulated atmospheric CO2 concentrations with three independent surface CO2 measurements in China. Results show that with the addition of CONTRAIL CO2 data, the inverted carbon sink in China increases while those in South and Southeast Asia decrease. Meanwhile, the posterior uncertainties over these regions are all reduced (2-12%). CONTRAIL CO2 data also have a large effect on the inter-annual variation of carbon sinks in China, leading to a better correlation between the carbon sink and the annual mean climate factors. Evaluations against the CO2 measurements at three sites in China also show that the CONTRAIL CO2 measurements may have improved the inversion results.

Regional inversion of CO2 ecosystem fluxes from atmospheric measurements. Reliability of the uncertainty estimates

Energy Technology Data Exchange (ETDEWEB)

Broquet, G.; Chevallier, F.; Breon, F.M.; Yver, C.; Ciais, P.; Ramonet, M.; Schmidt, M. [Laboratoire des Sciences du Climat et de l' Environnement, CEA-CNRS-UVSQ, UMR8212, IPSL, Gif-sur-Yvette (France); Alemanno, M. [Servizio Meteorologico dell' Aeronautica Militare Italiana, Centro Aeronautica Militare di Montagna, Monte Cimone/Sestola (Italy); Apadula, F. [Research on Energy Systems, RSE, Environment and Sustainable Development Department, Milano (Italy); Hammer, S. [Universitaet Heidelberg, Institut fuer Umweltphysik, Heidelberg (Germany); Haszpra, L. [Hungarian Meteorological Service, Budapest (Hungary); Meinhardt, F. [Federal Environmental Agency, Kirchzarten (Germany); Necki, J. [AGH University of Science and Technology, Krakow (Poland); Piacentino, S. [ENEA, Laboratory for Earth Observations and Analyses, Palermo (Italy); Thompson, R.L. [Max Planck Institute for Biogeochemistry, Jena (Germany); Vermeulen, A.T. [Energy research Centre of the Netherlands ECN, EEE-EA, Petten (Netherlands)

2013-07-01

The Bayesian framework of CO2 flux inversions permits estimates of the retrieved flux uncertainties. Here, the reliability of these theoretical estimates is studied through a comparison against the misfits between the inverted fluxes and independent measurements of the CO2 Net Ecosystem Exchange (NEE) made by the eddy covariance technique at local (few hectares) scale. Regional inversions at 0.5{sup 0} resolution are applied for the western European domain where {approx}50 eddy covariance sites are operated. These inversions are conducted for the period 2002-2007. They use a mesoscale atmospheric transport model, a prior estimate of the NEE from a terrestrial ecosystem model and rely on the variational assimilation of in situ continuous measurements of CO2 atmospheric mole fractions. Averaged over monthly periods and over the whole domain, the misfits are in good agreement with the theoretical uncertainties for prior and inverted NEE, and pass the chi-square test for the variance at the 30% and 5% significance levels respectively, despite the scale mismatch and the independence between the prior (respectively inverted) NEE and the flux measurements. The theoretical uncertainty reduction for the monthly NEE at the measurement sites is 53% while the inversion decreases the standard deviation of the misfits by 38 %. These results build confidence in the NEE estimates at the European/monthly scales and in their theoretical uncertainty from the regional inverse modelling system. However, the uncertainties at the monthly (respectively annual) scale remain larger than the amplitude of the inter-annual variability of monthly (respectively annual) fluxes, so that this study does not engender confidence in the inter-annual variations. The uncertainties at the monthly scale are significantly smaller than the seasonal variations. The seasonal cycle of the inverted fluxes is thus reliable. In particular, the CO2 sink period over the European continent likely ends later than

The Abundance of Atmospheric CO{sub 2} in Ocean Exoplanets: a Novel CO{sub 2} Deposition Mechanism

Energy Technology Data Exchange (ETDEWEB)

Levi, A.; Sasselov, D. [Harvard-Smithsonian Center for Astrophysics, 60 Garden Street, Cambridge, MA 02138 (United States); Podolak, M., E-mail: amitlevi.planetphys@gmail.com [Dept. of Geosciences, Tel Aviv University, Tel Aviv, 69978 (Israel)

2017-03-20

We consider super-Earth sized planets which have a water mass fraction large enough to form an external mantle composed of high-pressure water-ice polymorphs and also lack a substantial H/He atmosphere. We consider such planets in their habitable zone, so that their outermost condensed mantle is a global, deep, liquid ocean. For these ocean planets, we investigate potential internal reservoirs of CO{sub 2}, the amount of CO{sub 2} dissolved in the ocean for the various saturation conditions encountered, and the ocean-atmosphere exchange flux of CO{sub 2}. We find that, in a steady state, the abundance of CO{sub 2} in the atmosphere has two possible states. When wind-driven circulation is the dominant CO{sub 2} exchange mechanism, an atmosphere of tens of bars of CO{sub 2} results, where the exact value depends on the subtropical ocean surface temperature and the deep ocean temperature. When sea-ice formation, acting on these planets as a CO{sub 2} deposition mechanism, is the dominant exchange mechanism, an atmosphere of a few bars of CO{sub 2} is established. The exact value depends on the subpolar surface temperature. Our results suggest the possibility of a negative feedback mechanism, unique to water planets, where a reduction in the subpolar temperature drives more CO{sub 2} into the atmosphere to increase the greenhouse effect.

Deep Sea Memory of High Atmospheric CO2 Concentration

Science.gov (United States)

Mathesius, Sabine; Hofmann, Matthias; Caldeira, Ken; Schellnhuber, Hans Joachim

2015-04-01

Carbon dioxide removal (CDR) from the atmosphere has been proposed as a powerful measure to mitigate global warming and ocean acidification. Planetary-scale interventions of that kind are often portrayed as "last-resort strategies", which need to weigh in if humankind keeps on enhancing the climate-system stock of CO2. Yet even if CDR could restore atmospheric CO2 to substantially lower concentrations, would it really qualify to undo the critical impacts of past emissions? In the study presented here, we employed an Earth System Model of Intermediate Complexity (EMIC) to investigate how CDR might erase the emissions legacy in the marine environment, focusing on pH, temperature and dissolved oxygen. Against a background of a world following the RCP8.5 emissions path ("business-as-usual") for centuries, we simulated the effects of two massive CDR interventions with CO2 extraction rates of 5 GtC yr-1 and 25 GtC yr-1, respectively, starting in 2250. We found that the 5 GtC yr-1 scheme would have only minor ameliorative influence on the oceans, even after several centuries of application. By way of contrast, the extreme 25 GtC yr-1 scheme eventually leads to tangible improvements. However, even with such an aggressive measure, past CO2 emissions leave a substantial legacy in the marine environment within the simulated period (i.e., until 2700). In summary, our study demonstrates that anthropogenic alterations of the oceans, caused by continued business-as-usual emissions, may not be reversed on a multi-centennial time scale by the most aspirational geoengineering measures. We also found that a transition from the RCP8.5 state to the state of a strong mitigation scenario (RCP2.6) is not possible, even under the assumption of extreme extraction rates (25 GtC yr-1). This is explicitly demonstrated by simulating additional scenarios, starting CDR already in 2150 and operating until the atmospheric CO2 concentration reaches 280 ppm and 180 ppm, respectively. The simulated

ISLSCP II Globalview: Atmospheric CO2 Concentrations

Data.gov (United States)

National Aeronautics and Space Administration — The GlobalView Carbon Dioxide (CO2) data product contains synchronized and smoothed time series of atmospheric CO2 concentrations at selected sites that were created...

Evaluation of factors affecting accurate measurements of atmospheric CO2 and CH4 by wavelength-scanned cavity ring-down spectroscopy

Science.gov (United States)

Nara, H.; Tanimoto, H.; Tohjima, Y.; Mukai, H.; Nojiri, Y.; Katsumata, K.; Rella, C.

2012-07-01

We examined potential interferences from water vapor and atmospheric background gases (N2, O2, and Ar), and biases by isotopologues of target species, on accurate measurement of atmospheric CO2 and CH4 by means of wavelength-scanned cavity ring-down spectroscopy (WS-CRDS). Variations in the composition of the background gas substantially impacted the CO2 and CH4 measurements: the measured amounts of CO2 and CH4 decreased with increasing N2 mole fraction, but increased with increasing O2 and Ar, suggesting that the pressure-broadening effects (PBEs) increased as Ar < O2 < N2. Using these experimental results, we inferred PBEs for the measurement of synthetic standard gases. The PBEs were negligible (up to 0.05 ppm for CO2 and 0.01 ppb for CH4) for gas standards balanced with purified air, although the PBEs were substantial (up to 0.87 ppm for CO2 and 1.4 ppb for CH4) for standards balanced with synthetic air. For isotopic biases on CO2 measurements, we compared experimental results and theoretical calculations, which showed excellent agreement within their uncertainty. We derived empirical correction functions for water vapor for three WS-CRDS instruments (Picarro EnviroSense 3000i, G-1301, and G-2301). Although the transferability of the functions was not clear, no significant difference was found in the water vapor correction values among these instruments within the typical analytical precision at sufficiently low water concentrations (< 0.3%V for CO2 and < 0.4%V for CH4). For accurate measurements of CO2 and CH4 in ambient air, we concluded that WS-CRDS measurements should be performed under complete dehumidification of air samples, or moderate dehumidification followed by application of a water vapor correction function, along with calibration by natural air-based standard gases or purified air-balanced synthetic standard gases with isotopic correction.

Effects of atmospheric CO2 enrichment on soil CO2 efflux in a young longleaf pine system

Science.gov (United States)

Elevated atmospheric carbon dioxide (CO2) can affect the quantity and quality of plant tissues which will impact carbon (C) cycling and storage in plant/soil systems and the release of CO2 back to the atmosphere. Research is needed to quantify the effects of elevated CO2 on soil CO2 efflux to predi...

Capture of atmospheric CO2 into (BiO)2CO3/graphene or graphene oxide nanocomposites with enhanced photocatalytic performance

International Nuclear Information System (INIS)

Zhang, Wendong; Dong, Fan; Zhang, Wei

2015-01-01

Graphical abstract: Self-assembly of (BiO) 2 CO 3 nanoflakes on graphene and graphene oxide nanosheets were realized by a one-pot efficient capture of atmospheric CO 2 at room temperature. - Highlights: • A facile one-step method was developed for graphene-based composites. • The synthesis was conducted by utilization of atmospheric CO 2 . • (BiO) 2 CO 3 -graphene and (BiO) 2 CO 3 -graphene oxide composites were synthesized. • The nanocomposites exhibited enhanced photocatalytic activity. - Abstract: Self-assembly of (BiO) 2 CO 3 nanoflakes on graphene (Ge) and graphene oxide (GO) nanosheets, as an effective strategy to improve the photocatalytic performance of two-dimensional (2D) nanostructured materials, were realized by a one-pot efficient capture of atmospheric CO 2 at room temperature. The as-synthesized samples were characterized by XRD, SEM, TEM, XPS, UV–vis DRS, Time-resolved ns-level PL and BET-BJH measurement. The photocatalytic activity of the obtained samples was evaluated by the removal of NO at the indoor air level under simulated solar-light irradiation. Compared with pure (BiO) 2 CO 3 , (BiO) 2 CO 3 /Ge and (BiO) 2 CO 3 /GO nanocomposites exhibited enhanced photocatalytic activity due to their large surface areas and pore volume, and efficient charge separation and transfer. The present work could provide a simple method to construct 2D nanocomposites by efficient utilization of CO 2 in green synthetic strategy.

Comparisons of continuous atmospheric CH4, CO2 and N2O measurements - results from a travelling instrument campaign at Mace Head

International Nuclear Information System (INIS)

Vardag, S.N.; Hammer, S.; Levin, I.; O'Doherty, S.; Spain, T.G.; Wastine, B.; Jordan, A.

2014-01-01

A 2-month measurement campaign with a Fourier transform infrared analyser as a travelling comparison instrument (TCI) was performed at the Advanced Global Atmospheric Gases Experiment (AGAGE) and World Meteorological Organization (WMO) Global Atmosphere Watch (GAW) station at Mace Head, Ireland. The aim was to evaluate the compatibility of atmospheric methane (CH 4 ), carbon dioxide (CO 2 ) and nitrous oxide (N 2 O) measurements of the routine station instrumentation, consisting of a gas chromatograph (GC) for CH 4 and N 2 O as well as a cavity ring-down spectroscopy (CRDS) system for CH 4 and CO 2 . The advantage of a TCI approach for quality control is that the comparison covers the entire ambient air measurement system, including the sample intake system and the data evaluation process. For initial quality and performance control, the TCI was run in parallel with the Heidelberg GC before and after the measurement campaign at Mace Head. Median differences between the Heidelberg GC and the TCI were well within the WMO inter-laboratory compatibility target for all three greenhouse gases. At Mace Head, the median difference between the station GC and the TCI were -0.04 nmol mol -1 for CH 4 and -0.37 nmol mol -1 for N 2 O (GC-TCI). For N 2 O, a similar difference (-0.40 nmol mol -1 ) was found when measuring surveillance or working gas cylinders with both instruments. This suggests that the difference observed in ambient air originates from a calibration offset that could partly be due to a difference between the WMON2O X2006a reference scale used for the TCI and the Scripps Institution of Oceanography (SIO-1998) scale used at Mace Head and in the whole AGAGE network. Median differences between the CRDS G1301 and the TCI at Mace Head were 0.12 nmol mol -1 for CH 4 and 0.14 μmol mol -1 for CO 2 (CRDS G1301 - TCI). The difference between both instruments for CO 2 could not be explained, as direct measurements of calibration gases show no such difference. The CH 4

Current 2-μm dial measurements of atmospheric CO2 and expected results from space using new MCT APDS

Science.gov (United States)

Dumas, A.; Gibert, F.; Rothman, J.; Édouart, D.; Le Mounier, F.; Cénac, C.

2017-11-01

In the framework of CO2 monitoring in the Atmospheric Boundary Layer (ABL), a ground-based 2-μm Differential Absorption Lidar (DIAL) has been developed at the Laboratoire de Météorologie Dynamique (LMD) in Palaiseau. In order to derive flux information, this system has been set up with coherent detection, which allows to combine CO2 density measurements with wind velocity measurements. On the other hand, new advances in the field of Mercury Cadmium Tellure (MCT) Avalanche Photodiodes (APDs) open the way for high-precision measurements in direct detection ultimately from space. In this study, we first report on state of the art measurements obtained with the current coherent DIAL system before presenting expected results for a similar laser transmitter equipped with MCT APDs. For this latter part, we use a numerical model which relies on APDs performance data provided by the Laboratoire d'Électronique et de Technologie de l'Information (LETI).

Do Continental Shelves Act as an Atmospheric CO2 Sink?

Science.gov (United States)

Cai, W.

2003-12-01

Recent air-to-sea CO2 flux measurements at several major continental shelves (European Atlantic Shelves, East China Sea and U.S. Middle Atlantic Bight) suggest that shelves may act as a one-way pump and absorb atmospheric CO2 into the ocean. These observations also favor the argument that continental shelves are autotrophic (i.e., net production of organic carbon, OC). The U.S. South Atlantic Bight (SAB) contrasts these findings in that it acts as a strong source of CO2 to the atmosphere while simultaneously exporting dissolved inorganic carbon (DIC) to the open ocean. We report pCO2, DIC, and alkalinity data from the SAB collected in 8 cruises along a transect from the shore to the shelf break in the central SAB. The shelf-wide net heterotrophy and carbon exports in the SAB are subsidized by the export of OC from the abundant intertidal marshes, which are a sink for atmospheric CO2. It is proposed here that the SAB represents a marsh-dominated heterotrophic ocean margin as opposed to river-dominated autotrophic margins. To further investigate why margins may behave differently in term of CO2 sink/source, the physical and biological conditions of several western boundary current margins are compared. Based on this and other studies, DIC export flux from margins to the open ocean must be significant in the overall global ocean carbon budget.

Atmosphere-soil-vegetation model including CO2 exchange processes: SOLVEG2

International Nuclear Information System (INIS)

Nagai, Haruyasu

2004-11-01

A new atmosphere-soil-vegetation model named SOLVEG2 (SOLVEG version 2) was developed to study the heat, water, and CO 2 exchanges between the atmosphere and land-surface. The model consists of one-dimensional multilayer sub-models for the atmosphere, soil, and vegetation. It also includes sophisticated processes for solar and long-wave radiation transmission in vegetation canopy and CO 2 exchanges among the atmosphere, soil, and vegetation. Although the model usually simulates only vertical variation of variables in the surface-layer atmosphere, soil, and vegetation canopy by using meteorological data as top boundary conditions, it can be used by coupling with a three-dimensional atmosphere model. In this paper, details of SOLVEG2, which includes the function of coupling with atmosphere model MM5, are described. (author)

Relationship between carbon-14 concentrations in tree-ring cellulose and atmospheric CO2

International Nuclear Information System (INIS)

Yamada, Yoshimune; Yasuike, Kaeko; Komura, Kazuhisa

2008-01-01

Concentrations of organically-bound 14 C in the tree-ring cellulose of a Japanese Cedar (Cryptomeria japonica) grown in a rural region of Kanazawa, Ishikawa prefecture, Japan (36.5degN, 136.7degE), were measured for the ring-years from 1989 to 1998 to study relationship between 14 C concentrations in tree-ring cellulose and atmospheric CO 2 in a narrow region. An interesting result in comparing our data of tree-ring cellulose with those of atmospheric CO 2 is that the 14 C concentration in tree-ring cellulose was close to the corresponding average from mid-June to early September of 14 C concentrations in atmospheric CO 2 . Furthermore, the 14 C concentrations in tree-ring cellulose were found to be merely influenced by the drastic decrease of 14 C concentrations in atmospheric CO 2 in winter, which might be caused by air pollution from the Asian continent and additional local fossil fuel contribution. These results suggest that the 14 C concentration in tree-ring cellulose for a given growing year reflects the 14 C concentrations of atmospheric CO 2 during the warm summer months. (author)

[Data processing and QA/QC of atmosphere CO2 and CH4 concentrations by a method of GC-FID in-situ measurement at Waliguan station].

Science.gov (United States)

Zhang, Fang; Zhou, Ling-Xi; Liu, Li-Xin; Fang, Shuang-Xi; Yao, Bo; Xu, Lin; Zhang, Xiao-Chun; Masarie, Kenneth A; Conway, Thomas J; Worthy, Douglas E J; Ernst, Michele

2010-10-01

To strengthen scientific management and sharing of greenhouse gas data obtained from atmospheric background stations in China, it is important to ensure the standardization of observations and establish the data treatment and quality control procedure so as to maintain consistency in atmospheric carbon dioxide (CO2) and methane (CH4) measurements from different background stations. An automated gas chromatographic system (Hewlett Packard 5890GC employing flame ionization detection) for in situ measurements of atmospheric CO2 and CH4 has been developed since 1994 at the China Global Atmosphere Watch Baseline Observatory at Mt. Waliguan, in Qinhai. In this study, processing and quality control flow of CO2 and CH4 data acquired by HP ChemStation are discussed in detail, including raw data acquisition, data merge, time series inspection, operator flag, principal investigator flag, and the comparison of the GC measurement with the flask method. Atmosphere CO2 and CH4 mixing ratios were separated as background and non-background data using a robust local regression method, approximately 72% and 44% observed values had been filtered as background data for CO2 and CH4, respectively. Comparison of the CO1 and CH, in situ data to the flask sampling data were in good agreement, the relative deviations are within +/- 0.5% for CO2 and for CH4. The data has been assimilated into global database (Globalview-CO2, Globalview-CH4), submitted to the World Data Centre for Greenhouse Gases (WDCGG), and applied to World Meteorological Organization (WMO) Greenhouse Gas Bulletin and assessment reports of the United Nations Intergovernmental Panel on Climate Change (IPCC).

Remotely operable compact instruments for measuring atmospheric CO2 and CH4 column densities at surface monitoring sites

Directory of Open Access Journals (Sweden)

I. Morino

2010-08-01

Full Text Available Remotely operable compact instruments for measuring atmospheric CO2 and CH4 column densities were developed in two independent systems: one utilizing a grating-based desktop optical spectrum analyzer (OSA with a resolution enough to resolve rotational lines of CO2 and CH4 in the regions of 1565–1585 and 1674–1682 nm, respectively; the other is an application of an optical fiber Fabry-Perot interferometer (FFPI to obtain the CO2 column density. Direct sunlight was collimated via a small telescope installed on a portable sun tracker and then transmitted through an optical fiber into the OSA or the FFPI for optical analysis. The near infrared spectra of the OSA were retrieved by a least squares spectral fitting algorithm. The CO2 and CH4 column densities deduced were in excellent agreement with those measured by a Fourier transform spectrometer with high resolution. The rovibronic lines in the wavelength region of 1570–1575 nm were analyzed by the FFPI. The I0 and I values in the Beer-Lambert law equation to obtain CO2 column density were deduced by modulating temperature of the FFPI, which offered column CO2 with the statistical error less than 0.2% for six hours measurement.

Role of Atmospheric CO2 in the Ice Ages (Invited)

Science.gov (United States)

Toggweiler, J. R.

2010-12-01

Ice cores from Antarctica provide our most highly resolved records of glacial-interglacial climate change. They feature big transitions every 100,000 years or so in which Antarctica warms by up to 10 deg. C while the level of atmospheric CO2 rises by up to 100 ppm. We have no other records like these from any other location, so the assumption is often made that the Earth's mean temperature varies like the temperatures in Antarctica. The striking co-variation between the two records is taken to mean 1) that there is a causal relationship between the global temperature and atmospheric CO2 and 2) that atmospheric CO2 is a powerful agent of climate change during the ice ages. The problem is that the mechanism most often invoked to explain the CO2 variations operates right next to Antarctica and, as such, provides a fairly direct way to explain the temperature variations in Antarctica as well. If so, Antarctic temperatures go up and down for the same reason that atmospheric CO2 goes up and down, in which case no causation can be inferred. Climate models suggest that the 100-ppm CO2 increases during the big transitions did not increase surface temperatures by more than 2 deg. C. This is not nearly enough to explain the observed variability. A better reason for thinking that atmospheric CO2 is important is that its temporal variations are concentrated in the 100,000-yr band. In my presentation I will argue that atmospheric CO2 is important because it has the longest time scale in the system. We observe empirically that atmospheric CO2 remains low for 50,000 years during the second half of each 100,000-yr cycle. The northern ice sheets become especially large toward the ends of these intervals, and it is large ice sheets that make the Earth especially cold. This leads me to conclude that atmospheric CO2 is important because of its slow and persistent influence on the northern ice sheets over the second half of each 100,000-yr cycle.

RELATIONSHIP BETWEEN ATMOSPHERIC CO_2 AND CH_4 CONCENTRATIONS AT SYOWA STATION, ANTARCTICA

OpenAIRE

アオキ, シュウジ; ナカザワ, タカキヨ; ムラヤマ, ショウヘイ; シミズ, アキラ; ハヤシ, マサヒコ; イワイ, クニモト; Shuhji, AOKI; Takakiyo, NAKAZAWA; Shohei, MURAYAMA; Akira, SHIMIZU; Masahiko, HAYASHI; Kunimoto, IWAI

1994-01-01

Precise measurements of the atmospheric CO_2 and CH_4 concentrations have been continued at Syowa Station since 1984 and 1987,respectively. Measured concentrations show secular increase, together with seasonal cycle and irregular variations. Negative correlation is clearly seen between the secular trends of the CO_2 and CH_4 concentrations. The increase rates of CO_2 and CH_4 show oscillations with periods of 2.3 to 2.8 years. The phases of the average seasonal cycles of CO_2 and CH_4 coincid...

Atmospheric verification of anthropogenic CO2 emission trends

Science.gov (United States)

Francey, Roger J.; Trudinger, Cathy M.; van der Schoot, Marcel; Law, Rachel M.; Krummel, Paul B.; Langenfelds, Ray L.; Paul Steele, L.; Allison, Colin E.; Stavert, Ann R.; Andres, Robert J.; Rödenbeck, Christian

2013-05-01

International efforts to limit global warming and ocean acidification aim to slow the growth of atmospheric CO2, guided primarily by national and industry estimates of production and consumption of fossil fuels. Atmospheric verification of emissions is vital but present global inversion methods are inadequate for this purpose. We demonstrate a clear response in atmospheric CO2 coinciding with a sharp 2010 increase in Asian emissions but show persisting slowing mean CO2 growth from 2002/03. Growth and inter-hemispheric concentration difference during the onset and recovery of the Global Financial Crisis support a previous speculation that the reported 2000-2008 emissions surge is an artefact, most simply explained by a cumulative underestimation (~ 9PgC) of 1994-2007 emissions; in this case, post-2000 emissions would track mid-range of Intergovernmental Panel on Climate Change emission scenarios. An alternative explanation requires changes in the northern terrestrial land sink that offset anthropogenic emission changes. We suggest atmospheric methods to help resolve this ambiguity.

Inter-annual and seasonal variations in transport to a measuring site in western Siberia, and their impact on the observed atmospheric CO2 mixing ratio

International Nuclear Information System (INIS)

Eneroth, Kristina

2002-01-01

Inter-annual and seasonal variations in atmospheric transport to a CO 2 measuring site in western Siberia were studied using three-dimensional trajectories. We identified large differences in transport between summer and winter, but also some differences between the years. Cluster analysis was applied to the trajectory data to determine to what degree different atmospheric flow patterns influence the variability of the atmospheric CO 2 mixing ratio. The observed CO 2 mixing ratio was also compared to observed CO 2 surface fluxes to study the impact of local sources and sinks. It was found that during July the correlation between atmospheric transport from distant source regions and CO 2 mixing ratios was poor. Furthermore the correlation was also weak between the CO 2 mixing ratio and the local eddy flux measurements. We conclude that the short-term variability in atmospheric CO 2 during summer probably is dominated by larger scale (tens up to one hundred kilometers) CO 2 surface fluxes and local meteorology. The weaker biogenic CO 2 fluxes during winter, resulted in CO 2 mixing ratios more clearly influenced by long-range transport Of CO 2 . However, the highest atmospheric CO 2 concentrations were not observed in connection with westerly winds representing transport of polluted air from Europe, but during periods with stagnant flow conditions. It was conjected that these high CO 2 mixing ratios were due to respired CO 2 trapped and accumulated in the lower parts of the planetary boundary layer. The mean duration for the identified flow patterns was in the order of two days, with a maximum duration of a week. This means that to have a chance to detect variations in CO 2 mixing ratio due to air mass changes the sampling frequency (e.g. flask samples and flight measurements) must be at least every other day. Our results show that the atmospheric transport varies with season, year and altitude. This, together with the heterogeneity of the source and sink regions are

Positive feedback between increasing atmospheric CO2 and ecosystem productivity

Science.gov (United States)

Gelfand, I.; Hamilton, S. K.; Robertson, G. P.

2009-12-01

Increasing atmospheric CO2 will likely affect both the hydrologic cycle and ecosystem productivity. Current assumptions that increasing CO2 will lead to increased ecosystem productivity and plant water use efficiency (WUE) are driving optimistic predictions of higher crop yields as well as greater availability of freshwater resources due to a decrease in evapotranspiration. The plant physiological response that drives these effects is believed to be an increase in carbon uptake either by (a) stronger CO2 gradient between the stomata and the atmosphere, or by (b) reduced CO2 limitation of enzymatic carboxylation within the leaf. The (a) scenario will lead to increased water use efficiency (WUE) in plants. However, evidence for increased WUE is mostly based on modeling studies, and experiments producing a short duration or step-wise increase in CO2 concentration (e.g. free-air CO2 enrichment). We hypothesize that the increase in atmospheric CO2 concentration is having a positive effect on ecosystem productivity and WUE. To investigate this hypothesis, we analyzed meteorological, ANPP, and soil CO2 flux datasets together with carbon isotopic ratio (13C/12C) of archived plant samples from the long term ecological research (LTER) program at Kellogg Biological Station. The datasets were collected between 1989 and 2007 (corresponding to an increase in atmospheric CO2 concentration of ~33 ppmv at Mauna Loa). Wheat (Triticum aestivum) samples taken from 1989 and 2007 show a significant decrease in the C isotope discrimination factor (Δ) over time. Stomatal conductance is directly related to Δ, and thus Δ is inversely related to plant intrinsic WUE (iWUE). Historical changes in the 13C/12C ratio (δ13C) in samples of a perennial forb, Canada goldenrod (Solidago canadensis), taken from adjacent successional fields, indicate changes in Δ upon uptake of CO2 as well. These temporal trends in Δ suggest a positive feedback between the increasing CO2 concentration in the

Concentrations and (delta)13C values of atmospheric CO2 from oceanic atmosphere through time: polluted and non-polluted areas

International Nuclear Information System (INIS)

Longinelli, Antonio; Selmo, Enrico; Lenaz, Renzo; Ori, Carlo

2005-01-01

CO 2 is one of the primary agents of global climate changes. The increase of atmospheric CO 2 concentration is essentially related to human-induced emissions and, particularly, to the burning of fossil fuel whose (delta) 13 C values are quite negative. Consequently, an increase of the CO 2 concentration in the atmosphere should be paralleled by a decrease of its (delta) 13 C. Continuous and/or spot measurements of CO 2 concentrations were repeatedly carried out during the last decade and in the same period of the year along hemispheric courses from Italy to Antarctica on a vessel of the Italian National Research Program in Antarctica. During these expeditions, discrete air samples were also collected in 4-l Pyrex flasks in order to carry out precise carbon isotope analyses on atmospheric CO 2 from different areas, including theoretically 'clean' open ocean areas, with the main purpose of comparing these open ocean results with the results obtained by the National Oceanic and Atmospheric Administration/World Meteorological Organization (NOAA/WMO) at land-based stations. According to the data obtained for these two variables, a relatively large atmospheric pollution is apparent in the Mediterranean area where the CO 2 concentration has reached the value of 384 ppmv while quite negative (delta) 13 C values have been measured only occasionally. In this area, southerly winds probably help to reduce the effect of atmospheric pollution even though, despite a large variability of CO 2 concentrations, these values are consistently higher than those measured in open ocean areas by a few ppmv to about 10 ppmv. A marked, though non-continuous, pollution is apparent in the area of the Bab-el-Mandeb strait where (delta) 13 C values considerably more negative than in the Central and Southern Red Sea were measured. The concentration of atmospheric CO 2 over the Central Indian Ocean increased from about 361 ppmv at the end of 1996 to about 373 ppmv at the end of 2003 (mean growth

STABILITY OF CO2 ATMOSPHERES ON DESICCATED M DWARF EXOPLANETS

International Nuclear Information System (INIS)

Gao, Peter; Hu, Renyu; Li, Cheng; Yung, Yuk L.; Robinson, Tyler D.

2015-01-01

We investigate the chemical stability of CO 2 -dominated atmospheres of desiccated M dwarf terrestrial exoplanets using a one-dimensional photochemical model. Around Sun-like stars, CO 2 photolysis by Far-UV (FUV) radiation is balanced by recombination reactions that depend on water abundance. Planets orbiting M dwarf stars experience more FUV radiation, and could be depleted in water due to M dwarfs’ prolonged, high-luminosity pre-main sequences. We show that, for water-depleted M dwarf terrestrial planets, a catalytic cycle relying on H 2 O 2 photolysis can maintain a CO 2 atmosphere. However, this cycle breaks down for atmospheric hydrogen mixing ratios <1 ppm, resulting in ∼40% of the atmospheric CO 2 being converted to CO and O 2 on a timescale of 1 Myr. The increased O 2 abundance leads to high O 3 concentrations, the photolysis of which forms another CO 2 -regenerating catalytic cycle. For atmospheres with <0.1 ppm hydrogen, CO 2 is produced directly from the recombination of CO and O. These catalytic cycles place an upper limit of ∼50% on the amount of CO 2 that can be destroyed via photolysis, which is enough to generate Earth-like abundances of (abiotic) O 2 and O 3 . The conditions that lead to such high oxygen levels could be widespread on planets in the habitable zones of M dwarfs. Discrimination between biological and abiotic O 2 and O 3 in this case can perhaps be accomplished by noting the lack of water features in the reflectance and emission spectra of these planets, which necessitates observations at wavelengths longer than 0.95 μm

Assessing filtering of mountaintop CO2 mole fractions for application to inverse models of biosphere-atmosphere carbon exchange

Directory of Open Access Journals (Sweden)

S. L. Heck

2012-02-01

Full Text Available There is a widely recognized need to improve our understanding of biosphere-atmosphere carbon exchanges in areas of complex terrain including the United States Mountain West. CO2 fluxes over mountainous terrain are often difficult to measure due to unusual and complicated influences associated with atmospheric transport. Consequently, deriving regional fluxes in mountain regions with carbon cycle inversion of atmospheric CO2 mole fraction is sensitive to filtering of observations to those that can be represented at the transport model resolution. Using five years of CO2 mole fraction observations from the Regional Atmospheric Continuous CO2 Network in the Rocky Mountains (Rocky RACCOON, five statistical filters are used to investigate a range of approaches for identifying regionally representative CO2 mole fractions. Test results from three filters indicate that subsets based on short-term variance and local CO2 gradients across tower inlet heights retain nine-tenths of the total observations and are able to define representative diel variability and seasonal cycles even for difficult-to-model sites where the influence of local fluxes is much larger than regional mole fraction variations. Test results from two other filters that consider measurements from previous and following days using spline fitting or sliding windows are overly selective. Case study examples showed that these windowing-filters rejected measurements representing synoptic changes in CO2, which suggests that they are not well suited to filtering continental CO2 measurements. We present a novel CO2 lapse rate filter that uses CO2 differences between levels in the model atmosphere to select subsets of site measurements that are representative on model scales. Our new filtering techniques provide guidance for novel approaches to assimilating mountain-top CO2 mole fractions in carbon cycle inverse models.

North America's net terrestrial CO2 exchange with the atmosphere 1990-2009

Science.gov (United States)

King, A. W.; Andres, R. J.; Davis, K. J.; Hafer, M.; Hayes, D. J.; Huntzinger, D. N.; de Jong, B.; Kurz, W. A.; McGuire, A. D.; Vargas, R.; Wei, Y.; West, T. O.; Woodall, C. W.

2015-01-01

Scientific understanding of the global carbon cycle is required for developing national and international policy to mitigate fossil fuel CO2 emissions by managing terrestrial carbon uptake. Toward that understanding and as a contribution to the REgional Carbon Cycle Assessment and Processes (RECCAP) project, this paper provides a synthesis of net land-atmosphere CO2 exchange for North America (Canada, United States, and Mexico) over the period 1990-2009. Only CO2 is considered, not methane or other greenhouse gases. This synthesis is based on results from three different methods: atmospheric inversion, inventory-based methods and terrestrial biosphere modeling. All methods indicate that the North American land surface was a sink for atmospheric CO2, with a net transfer from atmosphere to land. Estimates ranged from -890 to -280 Tg C yr-1, where the mean of atmospheric inversion estimates forms the lower bound of that range (a larger land sink) and the inventory-based estimate using the production approach the upper (a smaller land sink). This relatively large range is due in part to differences in how the approaches represent trade, fire and other disturbances and which ecosystems they include. Integrating across estimates, "best" estimates (i.e., measures of central tendency) are -472 ± 281 Tg C yr-1 based on the mean and standard deviation of the distribution and -360 Tg C yr-1 (with an interquartile range of -496 to -337) based on the median. Considering both the fossil fuel emissions source and the land sink, our analysis shows that North America was, however, a net contributor to the growth of CO2 in the atmosphere in the late 20th and early 21st century. With North America's mean annual fossil fuel CO2 emissions for the period 1990-2009 equal to 1720 Tg C yr-1 and assuming the estimate of -472 Tg C yr-1 as an approximation of the true terrestrial CO2 sink, the continent's source : sink ratio for this time period was 1720:472, or nearly 4:1.

VUV-absorption cross section of CO2 at high temperatures and impact on exoplanet atmospheres

Directory of Open Access Journals (Sweden)

Venot Olivia

2014-02-01

Full Text Available Ultraviolet (UV absorption cross sections are an essential ingredient of photochemical atmosphere models. Exoplanet searches have unveiled a large population of short-period objects with hot atmospheres, very different from what we find in our solar system. Transiting exoplanets whose atmospheres can now be studied by transit spectroscopy receive extremely strong UV fluxes and have typical temperatures ranging from 400 to 2500 K. At these temperatures, UV photolysis cross section data are severely lacking. Our goal is to provide high-temperature absorption cross sections and their temperature dependency for important atmospheric compounds. This study is dedicated to CO2, which is observed and photodissociated in exoplanet atmospheres. We performed these measurements for the 115 - 200 nm range at 300, 410, 480, and 550 K. In the 195 - 230 nm range, we worked at seven temperatures between 465 and 800 K. We found that the absorption cross section of CO2 is very sensitive to temperature, especially above 160 nm. Within the studied range of temperature, the CO2 cross section can vary by more than two orders of magnitude. This, in particular, makes the absorption of CO2 significant up to wavelengths as high as 230 nm, while it is negligible above 200 nm at 300 K. To investigate the influence of these new data on the photochemistry of exoplanets, we implemented the measured cross section into a 1D photochemical model. The model predicts that accounting for this temperature dependency of CO2 cross section can affect the computed abundances of NH3, CO2, and CO by one order of magnitude in the atmospheres of hot Jupiter and hot Neptune.

Los Angeles megacity: a high-resolution land–atmosphere modelling system for urban CO2 emissions

Directory of Open Access Journals (Sweden)

S. Feng

2016-07-01

Full Text Available Megacities are major sources of anthropogenic fossil fuel CO2 (FFCO2 emissions. The spatial extents of these large urban systems cover areas of 10 000 km2 or more with complex topography and changing landscapes. We present a high-resolution land–atmosphere modelling system for urban CO2 emissions over the Los Angeles (LA megacity area. The Weather Research and Forecasting (WRF-Chem model was coupled to a very high-resolution FFCO2 emission product, Hestia-LA, to simulate atmospheric CO2 concentrations across the LA megacity at spatial resolutions as fine as  ∼  1 km. We evaluated multiple WRF configurations, selecting one that minimized errors in wind speed, wind direction, and boundary layer height as evaluated by its performance against meteorological data collected during the CalNex-LA campaign (May–June 2010. Our results show no significant difference between moderate-resolution (4 km and high-resolution (1.3 km simulations when evaluated against surface meteorological data, but the high-resolution configurations better resolved planetary boundary layer heights and vertical gradients in the horizontal mean winds. We coupled our WRF configuration with the Vulcan 2.2 (10 km resolution and Hestia-LA (1.3 km resolution fossil fuel CO2 emission products to evaluate the impact of the spatial resolution of the CO2 emission products and the meteorological transport model on the representation of spatiotemporal variability in simulated atmospheric CO2 concentrations. We find that high spatial resolution in the fossil fuel CO2 emissions is more important than in the atmospheric model to capture CO2 concentration variability across the LA megacity. Finally, we present a novel approach that employs simultaneous correlations of the simulated atmospheric CO2 fields to qualitatively evaluate the greenhouse gas measurement network over the LA megacity. Spatial correlations in the atmospheric CO2 fields reflect the coverage of

What have we learned from intensive atmospheric sampling field programmes of CO2

International Nuclear Information System (INIS)

Lin, J.C.; Wofsy, S.C.; Daube, B.C.; Matross, D.M.; Chow, V.Y.; Gottlieb, E.; Pathmathevan, M.; Munger, J.W.

2006-01-01

The spatial and temporal gradients in atmospheric CO 2 contain signatures of carbon fluxes, and as part of inverse studies,these signatures have been combined with atmospheric models to infer carbon sources and sinks. However, such studies have yet to yield finer-scale, regional fluxes over the continent that can be linked to ecosystem processes and ground-based observations. The reasons for this gap are twofold: lack of atmospheric observations over the continent and model deficiencies in interpreting such observations. This paper describes a series of intensive atmospheric sampling field programmes designed as pilot experiments to bridge the observational gap over the continent and to help test and develop models to interpret these observations. We summarize recent results emerging from this work,outlining the role of the intensive atmospheric programmes in collecting CO 2 data in both the vertical and horizontal dimensions. These data: (1) quantitatively establish the spatial variability of CO 2 and the associated errors from neglecting this variability in models; (2) directly measure regional carbon fluxes from airmass-following experiments and (3) challenge models to reduce and account for uncertainties in atmospheric transport. We conclude with a look towards the future, outlining ways in which intensive atmospheric sampling can contribute towards advancing carbon science

Inter-annual and seasonal variations in transport to a measuring site in western Siberia, and their impact on the observed atmospheric CO{sub 2} mixing ratio

Energy Technology Data Exchange (ETDEWEB)

Eneroth, Kristina

2002-05-01

Inter-annual and seasonal variations in atmospheric transport to a CO{sub 2} measuring site in western Siberia were studied using three-dimensional trajectories. We identified large differences in transport between summer and winter, but also some differences between the years. Cluster analysis was applied to the trajectory data to determine to what degree different atmospheric flow patterns influence the variability of the atmospheric CO{sub 2} mixing ratio. The observed CO{sub 2} mixing ratio was also compared to observed CO{sub 2} surface fluxes to study the impact of local sources and sinks. It was found that during July the correlation between atmospheric transport from distant source regions and CO{sub 2} mixing ratios was poor. Furthermore the correlation was also weak between the CO{sub 2} mixing ratio and the local eddy flux measurements. We conclude that the short-term variability in atmospheric CO{sub 2} during summer probably is dominated by larger scale (tens up to one hundred kilometers) CO{sub 2} surface fluxes and local meteorology. The weaker biogenic CO{sub 2} fluxes during winter, resulted in CO{sub 2} mixing ratios more clearly influenced by long-range transport Of CO{sub 2}. However, the highest atmospheric CO{sub 2} concentrations were not observed in connection with westerly winds representing transport of polluted air from Europe, but during periods with stagnant flow conditions. It was conjected that these high CO{sub 2} mixing ratios were due to respired CO{sub 2} trapped and accumulated in the lower parts of the planetary boundary layer. The mean duration for the identified flow patterns was in the order of two days, with a maximum duration of a week. This means that to have a chance to detect variations in CO{sub 2} mixing ratio due to air mass changes the sampling frequency (e.g. flask samples and flight measurements) must be at least every other day. Our results show that the atmospheric transport varies with season, year and altitude

Evaluating Humidity and Sea Salt Disturbances on CO2 Flux Measurements

DEFF Research Database (Denmark)

Nilsson, Erik; Bergström, Hans; Rutgersson, Anna

2018-01-01

Global oceans are an important sink of atmospheric carbon dioxide (CO2). Therefore, understanding the air–sea flux of CO2 is a vital part in describing the global carbon balance. Eddy covariance (EC) measurements are often used to study CO2 fluxes from both land and ocean. Values of CO2 are usual...

Research on atmospheric CO2 remote sensing with open-path tunable diode laser absorption spectroscopy and comparison methods

Science.gov (United States)

Xin, Fengxin; Guo, Jinjia; Sun, Jiayun; Li, Jie; Zhao, Chaofang; Liu, Zhishen

2017-06-01

An open-path atmospheric CO2 measurement system was built based on tunable diode laser absorption spectroscopy (TDLAS). The CO2 absorption line near 2 μm was selected, measuring the atmospheric CO2 with direct absorption spectroscopy and carrying on the comparative experiment with multipoint measuring instruments of the open-path. The detection limit of the TDLAS system is 1.94×10-6. The calibration experiment of three AZ-7752 handheld CO2 measuring instruments was carried out with the Los Gatos Research gas analyzer. The consistency of the results was good, and the handheld instrument could be used in the TDLAS system after numerical calibration. With the contrast of three AZ-7752 and their averages, the correlation coefficients are 0.8828, 0.9004, 0.9079, and 0.9393 respectively, which shows that the open-path TDLAS has the best correlation with the average of three AZ-7752 and measures the concentration of atmospheric CO2 accurately. Multipoint measurement provides a convenient comparative method for open-path TDLAS.

On the causes of trends in the seasonal amplitude of atmospheric CO2.

Science.gov (United States)

Piao, Shilong; Liu, Zhuo; Wang, Yilong; Ciais, Philippe; Yao, Yitong; Peng, Shushi; Chevallier, Frédéric; Friedlingstein, Pierre; Janssens, Ivan A; Peñuelas, Josep; Sitch, Stephen; Wang, Tao

2018-02-01

No consensus has yet been reached on the major factors driving the observed increase in the seasonal amplitude of atmospheric CO 2 in the northern latitudes. In this study, we used atmospheric CO 2 records from 26 northern hemisphere stations with a temporal coverage longer than 15 years, and an atmospheric transport model prescribed with net biome productivity (NBP) from an ensemble of nine terrestrial ecosystem models, to attribute change in the seasonal amplitude of atmospheric CO 2 . We found significant (p 50°N), consistent with previous observations that the amplitude increased faster at Barrow (Arctic) than at Mauna Loa (subtropics). The multi-model ensemble mean (MMEM) shows that the response of ecosystem carbon cycling to rising CO 2 concentration (eCO 2 ) and climate change are dominant drivers of the increase in AMP P -T and AMP T -P in the high latitudes. At the Barrow station, the observed increase of AMP P -T and AMP T -P over the last 33 years is explained by eCO 2 (39% and 42%) almost equally than by climate change (32% and 35%). The increased carbon losses during the months with a net carbon release in response to eCO 2 are associated with higher ecosystem respiration due to the increase in carbon storage caused by eCO 2 during carbon uptake period. Air-sea CO 2 fluxes (10% for AMP P -T and 11% for AMP T -P ) and the impacts of land-use change (marginally significant 3% for AMP P -T and 4% for AMP T -P ) also contributed to the CO 2 measured at Barrow, highlighting the role of these factors in regulating seasonal changes in the global carbon cycle. © 2017 John Wiley & Sons Ltd.

Atmospheric 14C changes resulting from fossil fuel CO2 release and cosmic ray flux variability

International Nuclear Information System (INIS)

Stuiver, M.; Quay, P.D.

1981-01-01

A high-precision tree-ring record of the atmospheric 14 C levels between 1820 and 1954 is presented. Good agreement is obtained between measured and model calculated 19th and 20th century atmospheric δ 14 C levels when both fossil fuel CO 2 release and predicted natural variations in 14 C production are taken into account. The best fit is obtained by using a box-diffusion model with an oceanic eddy diffusion coefficient of 3 cm 2 /s, a CO 2 atmosphere-ocean gas exchange rate of 21 moles msup(-2) yrsup(-1) and biospheric residence time of 60 years. For trees in the state of Washington the measured 1949-1951 atmospheric δ 14 C level was 20.0 +- 1.2per mille below the 1855-1864 level. Model calculations indicate that in 1950 industrial CO 2 emissions are responsible for at least 85% of the δ 14 C decline, whereas natural variability accounts for the remaining 15%. (orig.)

"Atmospheric Measurements by Ultra-Light SpEctrometer" (AMULSE) dedicated to vertical profile measurements of greenhouse gases (CO2, CH4) under stratospheric balloons: instrumental development and field application.

Science.gov (United States)

Maamary, Rabih; Joly, Lilian; Decarpenterie, Thomas; Cousin, Julien; Dumelié, Nicolas; Grouiez, Bruno; Albora, Grégory; Chauvin, Nicolas; Miftah-El-Khair, Zineb; Legain, Dominique; Tzanos, Diane; Barrié, Joel; Moulin, Eric; Ramonet, Michel; Bréon, François-Marie; Durry, Georges

2016-04-01

Human activities disrupt natural biogeochemical cycles such as the carbon and contribute to an increase in the concentrations of the greenhouse gases (carbone dioxide and methane) in the atmosphere. The current atmospheric transport modeling (the vertical trade) still represents an important source of uncertainty in the determination of regional flows of greenhouse gases, which means that a good knowledge of the vertical distribution of CO2 is necessary to (1) make the link between the ground measurements and spatial measurements that consider an integrated concentration over the entire column of the atmosphere, (2) validate and if possible improve CO2 transport model to make the link between surface emissions and observed concentration. The aim of this work is to develop a lightweight instrument (based on mid-infrared laser spectrometry principles) for in-situ measuring at high temporal/spatial resolution (5 Hz) the vertical profiles of the CO2 and the CH4 using balloons (meteorological and BSO at high precision levels (costs and logistics flights. These laser spectrometers are built on recent instrumental developments. Several flights were successfully done in the region Champagne-Ardenne and in Canada recently. Aknowledgments: The authors acknowledge financial supports from CNES, CNRS défi instrumental and the region Champagne-Ardenne.

Potentialities of the atmospheric CO2 remote sensing thanks to static Fourier transform spectrometry

International Nuclear Information System (INIS)

Lacan, A.

2009-04-01

A global measurement of atmospheric CO 2 concentration is required to improve the prediction of the range of global warming. A satellite mission could provide such a measurement. CNES developed a new generation instrument dedicated to atmospheric sounding. It is a static Fourier transform spectrometer whose mass and size are smaller than those of classical spectrometers. The application of the concept for CO 2 sounding is studied thanks to an on ground experimental bread board representative of a satellite borne spectrometer. The CO 2 concentration is deduced from atmospheric spectra at 1.6 μm thanks to differential spectroscopy technique. The instrumental concept is presented. Then the conception of the spectrometer and the working procedure are described. A study of information content is done. Retrieval simulations show that an error of ±0.6 ppm can be expected, lower than the ±1 ppm goal. Finally the results of a measurement campaign are given. The retrieval precision is compatible with the objectives. Yet the instrument is also sensitive to disruptive parameters. For example deformations of the instrument could engender significant measurement errors. Instrument improvements are proposed to increase the retrieval precision. (author)

A joint global carbon inversion system using both CO2 and 13CO2 atmospheric concentration data

Science.gov (United States)

Chen, Jing M.; Mo, Gang; Deng, Feng

2017-03-01

Observations of 13CO2 at 73 sites compiled in the GLOBALVIEW database are used for an additional constraint in a global atmospheric inversion of the surface CO2 flux using CO2 observations at 210 sites (62 collocated with 13CO2 sites) for the 2002-2004 period for 39 land regions and 11 ocean regions. This constraint is implemented using prior CO2 fluxes estimated with a terrestrial ecosystem model and an ocean model. These models simulate 13CO2 discrimination rates of terrestrial photosynthesis and ocean-atmosphere diffusion processes. In both models, the 13CO2 disequilibrium between fluxes to and from the atmosphere is considered due to the historical change in atmospheric 13CO2 concentration. This joint inversion system using both13CO2 and CO2 observations is effectively a double deconvolution system with consideration of the spatial variations of isotopic discrimination and disequilibrium. Compared to the CO2-only inversion, this 13CO2 constraint on the inversion considerably reduces the total land carbon sink from 3.40 ± 0.84 to 2.53 ± 0.93 Pg C year-1 but increases the total oceanic carbon sink from 1.48 ± 0.40 to 2.36 ± 0.49 Pg C year-1. This constraint also changes the spatial distribution of the carbon sink. The largest sink increase occurs in the Amazon, while the largest source increases are in southern Africa, and Asia, where CO2 data are sparse. Through a case study, in which the spatial distribution of the annual 13CO2 discrimination rate over land is ignored by treating it as a constant at the global average of -14. 1 ‰, the spatial distribution of the inverted CO2 flux over land was found to be significantly modified (up to 15 % for some regions). The uncertainties in our disequilibrium flux estimation are 8.0 and 12.7 Pg C year-1 ‰ for land and ocean, respectively. These uncertainties induced the unpredictability of 0.47 and 0.54 Pg C year-1 in the inverted CO2 fluxes for land and ocean, respectively. Our joint inversion system is therefore

Estimation of Potential Source Region in Northeast Asia through Continuous In-Situ Measurement of Atmospheric CO2 at Gosan, Jeju Island, Korea

OpenAIRE

Fenji Jin; Jooil Kim; Kyung-Ryul Kim

2010-01-01

High-Precision (¡_0.1 ppm), high-frequency (hourly averaged) measurement of atmospheric carbon dioxide (CO2) was made at Gosan Station on Jeju Island, Korea, using a Non-dispersive Infrared (NDIR) analyzer calibrated with National Oceanic and Atmospheric Administration/Earth Sys tem Re search Laboratory standards. This paper presents the one-year results from these measurements, including discussions on data quality control and data selection, data characteristics through comparing with other...

Capture of atmospheric CO{sub 2} into (BiO){sub 2}CO{sub 3}/graphene or graphene oxide nanocomposites with enhanced photocatalytic performance

Energy Technology Data Exchange (ETDEWEB)

Zhang, Wendong [Department of Scientific Research Management, Chongqing Normal University, Chongqing, 401331 (China); Dong, Fan, E-mail: dfctbu@126.com [Chongqing Key Laboratory of Catalysis and Functional Organic Molecules, College of Environment and Resources, Chongqing Technology and Business University, Chongqing, 400067 (China); Zhang, Wei, E-mail: andyzhangwei@163.com [Chongqing Institute of Green and Intelligent Technology, Chinese Academy of Sciences, Chongqing 400714 (China)

2015-12-15

Graphical abstract: Self-assembly of (BiO){sub 2}CO{sub 3} nanoflakes on graphene and graphene oxide nanosheets were realized by a one-pot efficient capture of atmospheric CO{sub 2} at room temperature. - Highlights: • A facile one-step method was developed for graphene-based composites. • The synthesis was conducted by utilization of atmospheric CO{sub 2}. • (BiO){sub 2}CO{sub 3}-graphene and (BiO){sub 2}CO{sub 3}-graphene oxide composites were synthesized. • The nanocomposites exhibited enhanced photocatalytic activity. - Abstract: Self-assembly of (BiO){sub 2}CO{sub 3} nanoflakes on graphene (Ge) and graphene oxide (GO) nanosheets, as an effective strategy to improve the photocatalytic performance of two-dimensional (2D) nanostructured materials, were realized by a one-pot efficient capture of atmospheric CO{sub 2} at room temperature. The as-synthesized samples were characterized by XRD, SEM, TEM, XPS, UV–vis DRS, Time-resolved ns-level PL and BET-BJH measurement. The photocatalytic activity of the obtained samples was evaluated by the removal of NO at the indoor air level under simulated solar-light irradiation. Compared with pure (BiO){sub 2}CO{sub 3}, (BiO){sub 2}CO{sub 3}/Ge and (BiO){sub 2}CO{sub 3}/GO nanocomposites exhibited enhanced photocatalytic activity due to their large surface areas and pore volume, and efficient charge separation and transfer. The present work could provide a simple method to construct 2D nanocomposites by efficient utilization of CO{sub 2} in green synthetic strategy.

The millennial atmospheric lifetime of anthropogenic CO2

International Nuclear Information System (INIS)

Archer, D.

2008-01-01

The notion is pervasive in the climate science community and in the public at large that the climate impacts of fossil fuel CO 2 release will only persist for a few centuries. This conclusion has no basis in theory or models of the atmosphere/ocean carbon cycle, which we review here. The largest fraction of the CO 2 recovery will take place on time scales of centuries, as CO 2 invades the ocean, but a significant fraction of the fossil fuel CO 2 , ranging in published models in the literature from 20-60%, remains airborne for a thousand years or longer. Ultimate recovery takes place on time scales of hundreds of thousands of years, a geologic longevity typically associated in public perceptions with nuclear waste. The glacial/interglacial climate cycles demonstrate that ice sheets and sea level respond dramatically to millennial-timescale changes in climate forcing. There are also potential positive feedbacks in the carbon cycle, including methane hydrates in the ocean, and peat frozen in permafrost, that are most sensitive to the long tail of the fossil fuel CO 2 in the atmosphere

Atmospheric CO2 and abrupt climate change on submillennial timescales

Science.gov (United States)

Ahn, Jinho; Brook, Edward

2010-05-01

How atmospheric CO2 varies and is controlled on various time scales and under various boundary conditions is important for understanding how the carbon cycle and climate change are linked. Ancient air preserved in ice cores provides important information on past variations in atmospheric CO2. In particular, concentration records for intervals of abrupt climate change may improve understanding of mechanisms that govern atmospheric CO2. We present new multi-decadal CO2 records that cover Greenland stadial 9 (between Dansgaard-Oeschger (DO) events 8 and 9) and the abrupt cooling event at 8.2 ka. The CO2 records come from Antarctic ice cores but are well synchronized with Greenland ice core records using new high-resolution CH4 records,precisely defining the timing of CO2 change with respect to abrupt climate events in Greenland. Previous work showed that during stadial 9 (40~38 ka), CO2 rose by about 15~20 ppm over around 2,000 years, and at the same time temperatures in Antarctica increased. Dust proxies indicate a decrease in dust flux over the same period. With more detailed data and better age controls we now find that approximately half of the CO2 increase during stadial 9 occurred abruptly, over the course of decades to a century at ~39.6 ka. The step increase of CO2 is synchronous with a similar step increase of Antarctic isotopic temperature and a small abrupt change in CH4, and lags after the onset of decrease in dust flux by ~400 years. New atmospheric CO2 records at the well-known ~8.2 ka cooling event were obtained from Siple Dome ice core, Antarctica. Our preliminary CO2 data span 900 years and include 19 data points within the 8.2 ka cooling event, which persisted for ~160 years (Thomas et al., Quarternary Sci. Rev., 2007). We find that CO2 increased by 2~4 ppm during that cooling event. Further analyses will improve the resolution and better constrain the CO2 variability during other times in the early Holocene to determine if the variations observed

Toward consistency between trends in bottom-up CO2 emissions and top-down atmospheric measurements in the Los Angeles megacity

Directory of Open Access Journals (Sweden)

S. Newman

2016-03-01

Full Text Available Large urban emissions of greenhouse gases result in large atmospheric enhancements relative to background that are easily measured. Using CO2 mole fractions and Δ14C and δ13C values of CO2 in the Los Angeles megacity observed in inland Pasadena (2006–2013 and coastal Palos Verdes peninsula (autumn 2009–2013, we have determined time series for CO2 contributions from fossil fuel combustion (Cff for both sites and broken those down into contributions from petroleum and/or gasoline and natural gas burning for Pasadena. We find a 10 % reduction in Pasadena Cff during the Great Recession of 2008–2010, which is consistent with the bottom-up inventory determined by the California Air Resources Board. The isotopic variations and total atmospheric CO2 from our observations are used to infer seasonality of natural gas and petroleum combustion. The trend of CO2 contributions to the atmosphere from natural gas combustion is out of phase with the seasonal cycle of total natural gas combustion seasonal patterns in bottom-up inventories but is consistent with the seasonality of natural gas usage by the area's electricity generating power plants. For petroleum, the inferred seasonality of CO2 contributions from burning petroleum is delayed by several months relative to usage indicated by statewide gasoline taxes. Using the high-resolution Hestia-LA data product to compare Cff from parts of the basin sampled by winds at different times of year, we find that variations in observed fossil fuel CO2 reflect seasonal variations in wind direction. The seasonality of the local CO2 excess from fossil fuel combustion along the coast, on Palos Verdes peninsula, is higher in autumn and winter than spring and summer, almost completely out of phase with that from Pasadena, also because of the annual variations of winds in the region. Variations in fossil fuel CO2 signals are consistent with sampling the bottom-up Hestia-LA fossil CO2 emissions product for sub

Water loss from terrestrial planets with CO2-rich atmospheres

International Nuclear Information System (INIS)

Wordsworth, R. D.; Pierrehumbert, R. T.

2013-01-01

Water photolysis and hydrogen loss from the upper atmospheres of terrestrial planets is of fundamental importance to climate evolution but remains poorly understood in general. Here we present a range of calculations we performed to study the dependence of water loss rates from terrestrial planets on a range of atmospheric and external parameters. We show that CO 2 can only cause significant water loss by increasing surface temperatures over a narrow range of conditions, with cooling of the middle and upper atmosphere acting as a bottleneck on escape in other circumstances. Around G-stars, efficient loss only occurs on planets with intermediate CO 2 atmospheric partial pressures (0.1-1 bar) that receive a net flux close to the critical runaway greenhouse limit. Because G-star total luminosity increases with time but X-ray and ultraviolet/ultravoilet luminosity decreases, this places strong limits on water loss for planets like Earth. In contrast, for a CO 2 -rich early Venus, diffusion limits on water loss are only important if clouds caused strong cooling, implying that scenarios where the planet never had surface liquid water are indeed plausible. Around M-stars, water loss is primarily a function of orbital distance, with planets that absorb less flux than ∼270 W m –2 (global mean) unlikely to lose more than one Earth ocean of H 2 O over their lifetimes unless they lose all their atmospheric N 2 /CO 2 early on. Because of the variability of H 2 O delivery during accretion, our results suggest that many 'Earth-like' exoplanets in the habitable zone may have ocean-covered surfaces, stable CO 2 /H 2 O-rich atmospheres, and high mean surface temperatures.

Simulated effect of calcification feedback on atmospheric CO2 and ocean acidification

Science.gov (United States)

Zhang, Han; Cao, Long

2016-01-01

Ocean uptake of anthropogenic CO2 reduces pH and saturation state of calcium carbonate materials of seawater, which could reduce the calcification rate of some marine organisms, triggering a negative feedback on the growth of atmospheric CO2. We quantify the effect of this CO2-calcification feedback by conducting a series of Earth system model simulations that incorporate different parameterization schemes describing the dependence of calcification rate on saturation state of CaCO3. In a scenario with SRES A2 CO2 emission until 2100 and zero emission afterwards, by year 3500, in the simulation without CO2-calcification feedback, model projects an accumulated ocean CO2 uptake of 1462 PgC, atmospheric CO2 of 612 ppm, and surface pH of 7.9. Inclusion of CO2-calcification feedback increases ocean CO2 uptake by 9 to 285 PgC, reduces atmospheric CO2 by 4 to 70 ppm, and mitigates the reduction in surface pH by 0.003 to 0.06, depending on the form of parameterization scheme used. It is also found that the effect of CO2-calcification feedback on ocean carbon uptake is comparable and could be much larger than the effect from CO2-induced warming. Our results highlight the potentially important role CO2-calcification feedback plays in ocean carbon cycle and projections of future atmospheric CO2 concentrations. PMID:26838480

Coral reefs - sources or sinks of atmospheric CO[sub 2

Energy Technology Data Exchange (ETDEWEB)

Ware, J R; Smith, S V; Reakakudla, M L [Hawaii University, Honolulu, HI (USA). Dept. of Oceanography

1992-09-01

Because the precipitation of calcium carbonate results in the sequestering of carbon, it frequently has been thought that coral reefs function as sinks of global atmospheric CO[sub 2]. However, the precipitation of calcium carbonate is accompanied by a shift of pH that results in the release of CO[sub 2]. This release of CO[sub 2] is less in buffered sea water than fresh water systems; nevertheless, coral reefs are sources, not sinks, of atmospheric carbon. Using estimated rates of coral reef carbonate production, we compute that coral reefs release 0.02 to 0.08 Gt C as CO[sub 2] annually. This is approximately 0.4% to 1.4% of the current anthropogenic CO[sub 2] production due to fossil fuel combustion.

Retrieval of average CO2 fluxes by combining in situ CO2 measurements and backscatter lidar information

Science.gov (United States)

Gibert, Fabien; Schmidt, Martina; Cuesta, Juan; Ciais, Philippe; Ramonet, Michel; Xueref, IrèNe; Larmanou, Eric; Flamant, Pierre Henri

2007-05-01

The present paper deals with a boundary layer budgeting method which makes use of observations from various in situ and remote sensing instruments to infer regional average net ecosystem exchange (NEE) of CO2. Measurements of CO2 within and above the atmospheric boundary layer (ABL) by in situ sensors, in conjunction with a precise knowledge of the change in ABL height by lidar and radiosoundings, enable to infer diurnal and seasonal NEE variations. Near-ground in situ CO measurements are used to discriminate natural and anthropogenic contributions of CO2 diurnal variations in the ABL. The method yields mean NEE that amounts to 5 μmol m-2 s-1 during the night and -20 μmol m-2 s-1 in the middle of the day between May and July. A good agreement is found with the expected NEE accounting for a mixed wheat field and forest area during winter season, representative of the mesoscale ecosystems in the Paris area according to the trajectory of an air column crossing the landscape. Daytime NEE is seen to follow the vegetation growth and the change in the ratio diffuse/direct radiation. The CO2 vertical mixing flux during the rise of the atmospheric boundary layer is also estimated and seems to be the main cause of the large decrease of CO2 mixing ratio in the morning. The outcomes on CO2 flux estimate are compared to eddy-covariance measurements on a barley field. The importance of various sources of error and uncertainty on the retrieval is discussed. These errors are estimated to be less than 15%; the main error resulted from anthropogenic emissions.

Six years of atmospheric CO2 observations at Mt. Fuji recorded with a battery-powered measurement system

Science.gov (United States)

Nomura, Shohei; Mukai, Hitoshi; Terao, Yukio; Machida, Toshinobu; Nojiri, Yukihiro

2017-03-01

We developed a battery-powered carbon dioxide (CO2) measurement system for monitoring at the summit of Mt. Fuji (3776 m a.s.l.), which experiences very low temperatures (below -20 °C) and severe environmental conditions without access to gridded electricity for 10 months (from September to June). Our measurement system used 100 batteries to run the measurement unit during these months. These batteries were charged during the 2-month summer season when gridded electricity was available, using a specially designed automatic battery-charging system. We installed this system in summer 2009 at the Mt. Fuji weather station; observations of atmospheric CO2 concentration were taken through December 2015. Measurements were never interrupted by a lack of battery power except for two cases in which lightning damaged a control board. Thus we obtained CO2 data during about 94 % of the 6-year period. Analytical performances (stability and accuracy) were better than 0.1 ppm, as tested by checking working standards and comparisons with flask sampling.Observational results showed that CO2 mole fractions at Mt. Fuji demonstrated clear seasonal variation. The trend and the variability of the CO2 growth rate observed at Mt. Fuji were very similar to those of the Mauna Loa Observatory (MLO). Seasonally, the concentration at Mt. Fuji was 2-10 ppm lower in summer and 2-12 ppm higher in winter than those at MLO. The lower concentrations at Mt. Fuji in summer are mainly attributed to episodes of air mass transport from Siberia or China, where CO2 is taken up by the terrestrial biosphere. On the other hand, the relatively higher concentrations in winter seem to reflect the high percentage of air masses originating from China or Southeast Asia during this period, which carry increased anthropogenic carbon dioxide. These results show that Mt. Fuji is not very influenced by local sources but rather by the sources and sinks over a very large region.Thus we conclude that, as this system could

Response of ocean acidification to a gradual increase and decrease of atmospheric CO2

International Nuclear Information System (INIS)

Cao, Long; Zhang, Han; Zheng, Meidi; Wang, Shuangjing

2014-01-01

We perform coupled climate–carbon cycle model simulations to examine changes in ocean acidity in response to idealized change of atmospheric CO 2 . Atmospheric CO 2 increases at a rate of 1% per year to four times its pre-industrial level of 280 ppm and then decreases at the same rate to the pre-industrial level. Our simulations show that changes in surface ocean chemistry largely follow changes in atmospheric CO 2 . However, changes in deep ocean chemistry in general lag behind the change in atmospheric CO 2 because of the long time scale associated with the penetration of excess CO 2 into the deep ocean. In our simulations with the effect of climate change, when atmospheric CO 2 reaches four times its pre-industrial level, global mean aragonite saturation horizon (ASH) shoals from the pre-industrial value of 1288 to 143 m. When atmospheric CO 2 returns from the peak value of 1120 ppm to pre-industrial level, ASH is 630 m, which is approximately the value of ASH when atmospheric CO 2 first increases to 719 ppm. At pre-industrial CO 2 9% deep-sea cold-water corals are surrounded by seawater that is undersaturated with aragonite. When atmospheric CO 2 reaches 1120 ppm, 73% cold-water coral locations are surrounded by seawater with aragonite undersaturation, and when atmospheric CO 2 returns to the pre-industrial level, 18% cold-water coral locations are surrounded by seawater with aragonite undersaturation. Our analysis indicates the difficulty for some marine ecosystems to recover to their natural chemical habitats even if atmospheric CO 2 content can be lowered in the future. (paper)

Developing a passive trap for diffusive atmospheric {sup 14}CO{sub 2} sampling

Energy Technology Data Exchange (ETDEWEB)

Walker, Jennifer C.; Xu, Xiaomei [Department of Earth System Science, University of California, Irvine, Irvine, CA (United States); Fahrni, Simon M. [Department of Earth System Science, University of California, Irvine, Irvine, CA (United States); Institute of Particle Physics, ETH, Zurich (Switzerland); Lupascu, Massimo [Department of Earth System Science, University of California, Irvine, Irvine, CA (United States); Department of Geography, National University of Singapore (Singapore); Czimczik, Claudia I. [Department of Earth System Science, University of California, Irvine, Irvine, CA (United States)

2015-10-15

{sup 14}C-CO{sub 2} measurement is an unique tool to quantify source-based emissions of CO{sub 2} for both the urban and natural environments. Acquiring a sample that temporally integrates the atmospheric {sup 14}C-CO{sub 2} signature that allows for precise {sup 14}C analysis is often necessary, but can require complex sampling devices, which can be difficult to deploy and maintain, especially for multiple locations. Here we describe our progress in developing a diffusive atmospheric CO{sub 2} molecular sieve trap, which requires no power to operate. We present results from various cleaning procedures, and rigorously tested for blank and memory effects. Traps were tested in the environment along-side conventional sampling flasks for accuracy. Results show that blank and memory effects can be minimized with thorough cleaning and by avoiding overheating, and that diffusively collected air samples agree well with traditionally canister-sampled air.

Experimental and Numerical Modelling of CO2 Atmospheric Dispersion in Hazardous Gas Emission Sites.

Science.gov (United States)

Gasparini, A.; sainz Gracia, A. S.; Grandia, F.; Bruno, J.

2015-12-01

Under stable atmospheric conditions and/or in presence of topographic depressions, CO2 concentrations can reach high values resulting in lethal effect to living organisms. The distribution of denser than air gases released from the underground is governed by gravity, turbulence and dispersion. Once emitted, the gas distribution is initially driven by buoyancy and a gas cloud accumulates on the ground (gravitational phase); with time the density gradient becomes less important due to dispersion or mixing and gas distribution is mainly governed by wind and atmospheric turbulence (passive dispersion phase). Natural analogues provide evidences of the impact of CO2 leakage. Dangerous CO2 concentration in atmosphere related to underground emission have been occasionally reported although the conditions favouring the persistence of such a concentration are barely studied.In this work, the dynamics of CO2 in the atmosphere after ground emission is assessed to quantify their potential risk. Two approaches have been followed: (1) direct measurement of air concentration in a natural emission site, where formation of a "CO2 lake" is common and (2) numerical atmospheric modelling. Two sites with different morphology were studied: (a) the Cañada Real site, a flat terrain in the Volcanic Field of Campo de Calatrava (Spain); (b) the Solforata di Pomezia site, a rough terrain in the Alban Hills Volcanic Region (Italy). The comparison between field data and model calculations reveal that numerical dispersion models are capable of predicting the formation of CO2 accumulation over the ground as a consequence of underground gas emission. Therefore, atmospheric modelling could be included as a valuable methodology in the risk assessment of leakage in natural degassing systems and in CCS projects. Conclusions from this work provide clues on whether leakage may be a real risk for humans and under which conditions this risk needs to be included in the risk assessment.

Assessment of MFLL column CO2 measurements obtained during the ACT-America field campaigns

Science.gov (United States)

Lin, B.; Browell, E. V.; Kooi, S. A.; Dobler, J. T.; Campbell, J.; Fan, T. F.; Pal, S.; O'Dell, C. W.; Obland, M. D.; Erxleben, W. H.; McGregor, D.; Kochanov, R. V.; DiGangi, J. P.; Davis, K. J.; Choi, Y.

2017-12-01

Accurate observations of atmospheric CO2 with airborne and space-based lidar systems such as those used during the Atmospheric Carbon and Transport - America (ACT-America) field campaigns and proposed for the NASA ASCENDS mission would improve our knowledge of CO2 distributions and variations on both regional and global scales, reduce the uncertainties in atmospheric CO2 transport and fluxes, and increase confidence in predictions of future climate changes. To reach these scientific goals, atmospheric column CO2 (XCO2) measurements of the Harris Corporation's Multifunctional Fiber Laser Lidar (MFLL) obtained during the first two ACT-America flight campaigns have been thoroughly investigated by the ACT-America lidar measurement group. MFLL is an intensity-modulated continuous-wave lidar operating in the 1.57-mm CO2 absorption band. Atmospheric XCO2 amounts are retrieved based on the integrated path differential absorption of the lidar signals at online and offline wavelengths between the aircraft and the ground. NASA Langley Research Center and Harris have been collaborating in the development and evaluation of this CO2 lidar approach for a number of years. To gain insights into the lidar performance, the measurement group has collected all possible lidar measurements with corresponding in-situ atmospheric profile information from the first two ACT-America field campaigns, including the data from several flight legs dedicated to lidar calibration. Initially large differences (-1 to 2 %) were found between lidar measured CO2 optical depths and those derived from in-situ observations and spectroscopy from HITRAN2008. When an improved spectroscopic model (Pre-HITRAN2016) was applied, the large systematic errors were much more consistent leading to the development of an empirical linear correction of measured optical depth based on the calibration flight data. This correction accounts for remaining uncertainties in spectroscopic models, environmental conditions, such as

Simulation of atmospheric CO2 over Europe and western Siberia using the regional scale model REMO

International Nuclear Information System (INIS)

Chevillard, A.; Ciais, P.; Lafont, S.

2002-01-01

The spatial distribution and the temporal variability of atmospheric CO 2 over Europe and western Siberia are investigated using the regional atmospheric model, REMO. The model, of typical horizontal resolution 50 km, is part of a nested modelling framework that has been established as a concerted action during the EUROSIBERIAN CARBONFLUX project. In REMO, the transport of CO 2 is simulated together with climate variables, which offers the possibility of calculating at each time step the land atmosphere CO 2 fluxes as driven by the modelled meteorology. The uptake of CO 2 by photosynthesis is calculated using a light use efficiency formulation, where the absorbed photosynthetically active solar radiation is inferred from satellite measurements. The release of CO 2 from plant and soil respiration is driven by the simulated climate and assumed to be in equilibrium with photosynthesis over the course of one year. Fossil CO 2 emissions and air-sea fluxes within the model domain are prescribed, whereas the influence of sources outside the model domain is computed from as a boundary condition CO 2 fields determined a global transport model. The modelling results are compared against pointwise eddy covariance fluxes, and against atmospheric CO 2 records. We show that a necessary condition to simulate realistically the variability of atmospheric CO 2 over continental Europe is to account for the diurnal cycle of biospheric exchange. Overall, for the study period of July 1998, REMO realistically simulates the short-term variability of fluxes and of atmospheric mixing ratios. However, the mean CO 2 gradients from western Europe to western Siberia are not correctly reproduced. This latter deficiency points out the key role of boundary conditions in a limited-area model, as well as the need for using more realistic geographic mean patterns of biospheric carbon fluxes

Carbon dioxide exchange between atmosphere and ocean and the question of an increase of atmospheric CO/sub 2/ during the past decades

Energy Technology Data Exchange (ETDEWEB)

Revelle, R; Suess, H E

1957-01-01

From a comparison of C/sup 14//C/sup 12/ and C/sup 13//C/sup 12/ ratios in wood and in marine material and from a slight decrease of the C/sup 14/ concentration in terrestrial plants over the past 50 years it can be concluded that the average lifetime of a CO/sub 2/ molecule in the atmosphere before it is dissolved into the sea is of the order of 10 years. This means that most of the CO/sub 2/ released by artificial fuel combustion since the beginning of the industrial revolution must have been absorbed by the oceans. The increase of atmospheric CO/sub 2/ from this cause is at present small but may become significant during future decades of industrial fuel combustion continues to rise exponentially. Present data on the total amount of CO/sub 2/ in the atmosphere, on the rates and mechanisms of exchange, and on possible fluctuations in terrestrial and marine organic carbon, are inadequate for accurate measurement of future changes in atmospheric CO/sub 2/. An opportunity exists during the international geophysical year to obtain much of the necessary information.

Atomic carbon emission from photodissociation of CO2. [planetary atmospheric chemistry

Science.gov (United States)

Wu, C. Y. R.; Phillips, E.; Lee, L. C.; Judge, D. L.

1978-01-01

Atomic carbon fluorescence, C I 1561, 1657, and 1931 A, has been observed from photodissociation of CO2, and the production cross sections have been measured. A line emission source provided the primary photons at wavelengths from threshold to 420 A. The present results suggest that the excited carbon atoms are produced by total dissociation of CO2 into three atoms. The cross sections for producing the O I 1304-A fluorescence through photodissociation of CO2 are found to be less than 0.01 Mb in the wavelength region from 420 to 835 A. The present data have implications with respect to photochemical processes in the atmospheres of Mars and Venus.

Compact and portable open-path sensor for simultaneous measurements of atmospheric N2O and CO using a quantum cascade laser.

Science.gov (United States)

Tao, Lei; Sun, Kang; Khan, M Amir; Miller, David J; Zondlo, Mark A

2012-12-17

A compact and portable open-path sensor for simultaneous detection of atmospheric N(2)O and CO has been developed with a 4.5 μm quantum cascade laser (QCL). An in-line acetylene (C(2)H(2)) gas reference cell allows for continuous monitoring of the sensor drift and calibration in rapidly changing field environments and thereby allows for open-path detection at high precision and stability. Wavelength modulation spectroscopy (WMS) is used to detect simultaneously both the second and fourth harmonic absorption spectra with an optimized dual modulation amplitude scheme. Multi-harmonic spectra containing atmospheric N(2)O, CO, and the reference C(2)H(2) signals are fit in real-time (10 Hz) by combining a software-based lock-in amplifier with a computationally fast numerical model for WMS. The sensor consumes ~50 W of power and has a mass of ~15 kg. Precision of 0.15 ppbv N(2)O and 0.36 ppbv CO at 10 Hz under laboratory conditions was demonstrated. The sensor has been deployed for extended periods in the field. Simultaneous N(2)O and CO measurements distinguished between natural and fossil fuel combustion sources of N(2)O, an important greenhouse gas with poorly quantified emissions in space and time.

North America's net terrestrial CO2 exchange with the atmosphere 1990–2009

Science.gov (United States)

King, A.W.; Andres, R.J.; Davis, K.J.; Hafer, M.; Hayes, D.J.; Huntzinger, Deborah N.; de Jong, Bernardus; Kurz, W.A.; McGuire, A. David; Vargas, Rodrigo I.; Wei, Y.; West, Tristram O.; Woodall, Christopher W.

2015-01-01

Scientific understanding of the global carbon cycle is required for developing national and international policy to mitigate fossil fuel CO2 emissions by managing terrestrial carbon uptake. Toward that understanding and as a contribution to the REgional Carbon Cycle Assessment and Processes (RECCAP) project, this paper provides a synthesis of net land–atmosphere CO2 exchange for North America (Canada, United States, and Mexico) over the period 1990–2009. Only CO2 is considered, not methane or other greenhouse gases. This synthesis is based on results from three different methods: atmospheric inversion, inventory-based methods and terrestrial biosphere modeling. All methods indicate that the North American land surface was a sink for atmospheric CO2, with a net transfer from atmosphere to land. Estimates ranged from −890 to −280 Tg C yr−1, where the mean of atmospheric inversion estimates forms the lower bound of that range (a larger land sink) and the inventory-based estimate using the production approach the upper (a smaller land sink). This relatively large range is due in part to differences in how the approaches represent trade, fire and other disturbances and which ecosystems they include. Integrating across estimates, "best" estimates (i.e., measures of central tendency) are −472 ± 281 Tg C yr−1 based on the mean and standard deviation of the distribution and −360 Tg C yr−1 (with an interquartile range of −496 to −337) based on the median. Considering both the fossil fuel emissions source and the land sink, our analysis shows that North America was, however, a net contributor to the growth of CO2 in the atmosphere in the late 20th and early 21st century. With North America's mean annual fossil fuel CO2 emissions for the period 1990–2009 equal to 1720 Tg C yr−1 and assuming the estimate of −472 Tg C yr−1 as an approximation of the true terrestrial CO2 sink, the continent's source : sink ratio for this time period was

Effects of Atmospheric CO2 Enrichment on Soil CO2 Efflux in a Young Longleaf Pine System

OpenAIRE

Runion, G. Brett; Butnor, J. R.; Prior, S. A.; Mitchell, R. J.; Rogers, H. H.

2012-01-01

The southeastern landscape is composed of agricultural and forest systems that can store carbon (C) in standing biomass and soil. Research is needed to quantify the effects of elevated atmospheric carbon dioxide (CO2) on terrestrial C dynamics including CO2 release back to the atmosphere and soil sequestration. Longleaf pine savannahs are an ecologically and economically important, yet understudied, component of the southeastern landscape. We investigated the effects of ambient and elevated C...

Return of the coral reef hypothesis: basin to shelf partitioning of CaCO3 and its effect on atmospheric CO2.

Science.gov (United States)

Opdyke, B N; Walker, J C

1992-08-01

Differences in the rate of coral reef carbonate deposition from the Pleistocene to the Holocene may account for the Quaternary variation of atmospheric CO2. Volumes of carbonate associated with Holocene reefs require an average deposition rate of 2.0 x 10(13) mol/yr for the past 5 ka. In light of combined riverine, midocean ridge, and ground-water fluxes of calcium to the oceans of 2.3 x 10(13) mol/yr, the current flux of calcium carbonate to pelagic sediments must be far below the Pleistocene average of 1.2 x 10(13) mol/yr. We suggest that sea-level change shifts the locus of carbonate deposition from the deep sea to the shelves as the normal glacial-interglacial pattern of deposition for Quaternary global carbonates. To assess the impact of these changes on atmospheric CO2, a simple numerical simulation of the global carbon cycle was developed. Atmospheric CO2 as well as calcite saturation depth and sediment responses to these carbonate deposition changes are examined. Atmospheric CO2 changes close to those observed in the Vostok ice core, approximately 80 ppm CO2, for the Quaternary are observed as well as the approximate depth changes in percent carbonate of sediments measured in the Pacific Ocean over the same time interval.

Reduced calcification of marine plankton in response to increased atmospheric CO2.

Science.gov (United States)

Riebesell, U; Zondervan, I; Rost, B; Tortell, P D; Zeebe, R E; Morel, F M

2000-09-21

The formation of calcareous skeletons by marine planktonic organisms and their subsequent sinking to depth generates a continuous rain of calcium carbonate to the deep ocean and underlying sediments. This is important in regulating marine carbon cycling and ocean-atmosphere CO2 exchange. The present rise in atmospheric CO2 levels causes significant changes in surface ocean pH and carbonate chemistry. Such changes have been shown to slow down calcification in corals and coralline macroalgae, but the majority of marine calcification occurs in planktonic organisms. Here we report reduced calcite production at increased CO2 concentrations in monospecific cultures of two dominant marine calcifying phytoplankton species, the coccolithophorids Emiliania huxleyi and Gephyrocapsa oceanica. This was accompanied by an increased proportion of malformed coccoliths and incomplete coccospheres. Diminished calcification led to a reduction in the ratio of calcite precipitation to organic matter production. Similar results were obtained in incubations of natural plankton assemblages from the north Pacific ocean when exposed to experimentally elevated CO2 levels. We suggest that the progressive increase in atmospheric CO2 concentrations may therefore slow down the production of calcium carbonate in the surface ocean. As the process of calcification releases CO2 to the atmosphere, the response observed here could potentially act as a negative feedback on atmospheric CO2 levels.

Modeling the transformation of atmospheric CO2 into microalgal biomass.

Science.gov (United States)

Hasan, Mohammed Fahad; Vogt, Frank

2017-10-23

Marine phytoplankton acts as a considerable sink of atmospheric CO 2 as it sequesters large quantities of this greenhouse gas for biomass production. To assess microalgae's counterbalancing of global warming, the quantities of CO 2 they fix need to be determined. For this task, it is mandatory to understand which environmental and physiological parameters govern this transformation from atmospheric CO 2 to microalgal biomass. However, experimental analyses are challenging as it has been found that the chemical environment has a major impact on the physiological properties of the microalgae cells (diameter typ. 5-20 μm). Moreover, the cells can only chemically interact with their immediate vicinity and thus compound sequestration needs to be studied on a microscopic spatial scale. Due to these reasons, computer simulations are a more promising approach than the experimental studies. Modeling software has been developed that describes the dissolution of atmospheric CO 2 into oceans followed by the formation of HCO 3 - which is then transported to individual microalgae cells. The second portion of this model describes the competition of different cell species for this HCO 3 - , a nutrient, as well as its uptake and utilization for cell production. Two microalgae species, i.e. Dunaliella salina and Nannochloropsis oculata, were cultured individually and in a competition situation under different atmospheric CO 2 conditions. It is shown that this novel model's predictions of biomass production are in very good agreement with the experimental flow cytometry results. After model validation, it has been applied to long-term prediction of phytoplankton generation. These investigations were motivated by the question whether or not cell production slows down as cultures grow. This is of relevance as a reduced cell production rate means that the increase in a culture's CO 2 -sinking capacity slows down as well. One implication resulting from this is that an increase in

Advanced Sine Wave Modulation of Continuous Wave Laser System for Atmospheric CO2 Differential Absorption Measurements

Science.gov (United States)

Campbell, Joel F.; Lin, Bing; Nehrir, Amin R.

2014-01-01

NASA Langley Research Center in collaboration with ITT Exelis have been experimenting with Continuous Wave (CW) laser absorption spectrometer (LAS) as a means of performing atmospheric CO2 column measurements from space to support the Active Sensing of CO2 Emissions over Nights, Days, and Seasons (ASCENDS) mission.Because range resolving Intensity Modulated (IM) CW lidar techniques presented here rely on matched filter correlations, autocorrelation properties without side lobes or other artifacts are highly desirable since the autocorrelation function is critical for the measurements of lidar return powers, laser path lengths, and CO2 column amounts. In this paper modulation techniques are investigated that improve autocorrelation properties. The modulation techniques investigated in this paper include sine waves modulated by maximum length (ML) sequences in various hardware configurations. A CW lidar system using sine waves modulated by ML pseudo random noise codes is described, which uses a time shifting approach to separate channels and make multiple, simultaneous online/offline differential absorption measurements. Unlike the pure ML sequence, this technique is useful in hardware that is band pass filtered as the IM sine wave carrier shifts the main power band. Both amplitude and Phase Shift Keying (PSK) modulated IM carriers are investigated that exibit perfect autocorrelation properties down to one cycle per code bit. In addition, a method is presented to bandwidth limit the ML sequence based on a Gaussian filter implemented in terms of Jacobi theta functions that does not seriously degrade the resolution or introduce side lobes as a means of reducing aliasing and IM carrier bandwidth.

[Open-path online monitoring of ambient atmospheric CO2 based on laser absorption spectrum].

Science.gov (United States)

He, Ying; Zhang, Yu-Jun; Kan, Rui-Feng; Xia, Hui; Geng, Hui; Ruan, Jun; Wang, Min; Cui, Xiao-Juan; Liu, Wen-Qing

2009-01-01

With the conjunction of tunable diode laser absorption spectroscopy technology (TDLAS) and the open long optical path technology, the system designing scheme of CO2 on-line monitoring based on near infrared tunable diode laser absorption spectroscopy technology was discussed in detail, and the instrument for large-range measurement was set up. By choosing the infrared absorption line of CO2 at 1.57 microm whose line strength is strong and suitable for measurement, the ambient atmospheric CO2 was measured continuously with a 30 s temporal resolution at an suburb site in the autumn of 2007. The diurnal atmospheric variations of CO2 and continuous monitoring results were presented. The results show that the variation in CO2 concentration has an obvious diurnal periodicity in suburb where the air is free of interference and contamination. The general characteristic of diurnal variation is that the concentration is low in the daytime and high at night, so it matches the photosynthesis trend. The instrument can detect gas concentration online with high resolution, high sensitivity, high precision, short response time and many other advantages, the monitoring requires no gas sampling, the calibration is easy, and the detection limit is about 4.2 x 10(-7). It has been proved that the system and measurement project are feasible, so it is an effective method for gas flux continuous online monitoring of large range in ecosystem based on TDLAS technology.

Atmospheric deposition, CO2, and change in the land carbon sink

DEFF Research Database (Denmark)

Martinez-Fernandez, Cristina; Vicca, Sara; Janssens, Ivan A.

2017-01-01

Concentrations of atmospheric carbon dioxide (CO2) have continued to increase whereas atmospheric deposition of sulphur and nitrogen has declined in Europe and the USA during recent decades. Using time series of flux observations from 23 forests distributed throughout Europe and the USA, and gene...... show the need to include the effects of changing atmospheric composition, beyond CO2, to assess future dynamics of carbon-climate feedbacks not currently considered in earth system/climate modelling....

Ventilation in Sewers Quantified by Measurements of CO2

DEFF Research Database (Denmark)

Fuglsang, Emil Dietz; Vollertsen, Jes; Nielsen, Asbjørn Haaning

2012-01-01

Understanding and quantifying ventilation in sewer systems is a prerequisite to predict transport of odorous and corrosive gasses within the system as well as their interaction with the urban atmosphere. This paper studies ventilation in sewer systems quantified by measurements of the natural...... occurring compound CO2. Most often Danish wastewater is supersaturated with CO2 and hence a potential for stripping is present. A novel model was built based on the kinetics behind the stripping process. It was applied to simulate ventilation rates from field measurements of wastewater temperature, p...

The role of vegetation dynamics in the control of atmospheric CO{sub 2} content

Energy Technology Data Exchange (ETDEWEB)

Sitch, Stephen

2000-04-01

This thesis contains a description of the Lund-Potsdam-Jena Dynamic Global Vegetation Model (LPJ-DGVM) and its application to infer the role of vegetation dynamics on atmospheric CO{sub 2} content at different time-scales. The model combines vegetation dynamics and biogeochemistry in a modular framework. Individual modules describe ecosystems processes, including vegetation resource competition and production, tissue turnover, growth, fire and mortality, soil and litter biogeochemistry, including the effects of CO{sub 2} on these processes. The model simulates realistic post-disturbance succession in different environments. Seasonal exchange of H{sub 2}O and CO{sub 2} between the terrestrial biosphere and the atmosphere is modelled in reasonable agreement with observation. Global estimates of carbon stocks in soil, litter and vegetation are within their acceptable ranges and the model captures the present-day patterns in vegetation. Fire return intervals are simulated correctly in most regions. Results emphasise the important role of the terrestrial biosphere in both the seasonal cycle and in the inter-annual variability in the growth rate of atmospheric CO{sub 2}. LPJ successfully reproduced both the amplitude and phase of the seasonal cycle of atmospheric CO{sub 2} content as measured at a global network of monitoring stations. The model predicted a small net terrestrial biosphere uptake of CO{sub 2} during the 1980s with a strong CO{sub 2} fertilisation effect, which enhances plant production, reduced by the effects of climate and land use change. Historical land use change and CO{sub 2} fertilisation have been the dominant, albeit opposing factors governing the response of the terrestrial biosphere with respect to carbon storage during the 20th century. LPJ is run using one future climate and atmospheric CO{sub 2} scenario until 2200. Enhanced production due to the CO{sub 2} fertilisation effect eventually reaches an asymptote, and consequently the ability of

CO2 deficit in temperate forest soils receiving high atmospheric N-deposition.

Science.gov (United States)

Fleischer, Siegfried

2003-02-01

Evidence is provided for an internal CO2 sink in forest soils, that may have a potential impact on the global CO2-budget. Lowered CO2 fraction in the soil atmosphere, and thus lowered CO2 release to the aboveground atmosphere, is indicated in high N-deposition areas. Also at forest edges, especially of spruce forest, where additional N-deposition has occurred, the soil CO2 is lowered, and the gradient increases into the closed forest. Over the last three decades the capacity of the forest soil to maintain the internal sink process has been limited to a cumulative supply of approximately 1000 and 1500 kg N ha(-1). Beyond this limit the internal soil CO2 sink becomes an additional CO2 source, together with nitrogen leaching. This stage of "nitrogen saturation" is still uncommon in closed forests in southern Scandinavia, however, it occurs in exposed forest edges which receive high atmospheric N-deposition. The soil CO2 gradient, which originally increases from the edge towards the closed forest, becomes reversed.

Responses of C4 grasses to atmospheric CO2 enrichment : I. Effect of irradiance.

Science.gov (United States)

Sionit, Nasser; Patterson, David T

1984-12-01

The growth and photosynethetic responses to atmospheric CO 2 enrichment of 4 species of C 4 grasses grown at two levels of irradiance were studied. We sought to determine whether CO 2 enrichment would yield proportionally greater growth enhancement in the C 4 grasses when they were grown at low irradiance than when grown at high irradiance. The species studied were Echinochloa crusgalli, Digitaria sanguinalis, Eleusine indica, and Setaria faberi. Plants were grown in controlled environment chambers at 350, 675 and 1,000 μl 1 -1 CO 2 and 1,000 or 150 μmol m -2 s -1 photosynthetic photon flux density (PPFD). An increase in CO 2 concentration and PPFD significantly affected net photosynthesis and total biomass production of all plants. Plants grown at low PPFD had significantly lower rates of photosynthesis, produced less biomass, and had reduced responses to increases in CO 2 . Plants grown in CO 2 -enriched atmosphere had lower photosynthetic capacity relative to the low CO 2 grown plants when exposed to lower CO 2 concentration at the time of measurement, but had greater rate of photosynthesis when exposed to increasing PPFD. The light level under which the plants were growing did not influence the CO 2 compensation point for photosynthesis.

Interannual variability in the oxygen isotopes of atmospheric CO2 driven by El Nino

NARCIS (Netherlands)

Welp, Lisa R.; Keeling, Ralph F.; Meijer, Harro A. J.; Bollenbacher, Alane F.; Piper, Stephen C.; Yoshimura, Kei; Francey, Roger J.; Allison, Colin E.; Wahlen, Martin

2011-01-01

The stable isotope ratios of atmospheric CO2 (O-18/O-16 and C-13/C-12) have been monitored since 1977 to improve our understanding of the global carbon cycle, because biosphere-atmosphere exchange fluxes affect the different atomic masses in a measurable way(1). Interpreting the O-18/O-16

TG-FTIR measurement of CO2-H2O co-adsorption for CO2 air capture sorbent screening

NARCIS (Netherlands)

Smal, I.M.; Yu, Qian; Veneman, Rens; Fränzel-Luiten, B.; Brilman, Derk Willem Frederik

2014-01-01

Capturing atmospheric CO2 using solid sorbents is gaining interest. As ambient air normally contains much more (up to 100 times) water than CO2, a selective sorbent is desirable as co-adsorption will most likely occur. In this study, a convenient method based on an TG-FTIR analysis system is

Measurement of OCS, CO2, CO and H2O aboard NASA's WB-57 High Altitude Platform Using Off-Axis Integrated Cavity Output Spectroscopy (OA-ICOS)

Science.gov (United States)

Leen, J. B.; Owano, T. G.; Du, X.; Gardner, A.; Gupta, M.

2014-12-01

Carbonyl sulfide (OCS) is the most abundant sulfur gas in the atmosphere and has been implicated in controlling the sulfur budget and aerosol loading of the stratosphere. In the troposphere, OCS is irreversibly consumed during photosynthesis and may serve as a tracer for gross primary production (GPP). Its primary sources are ocean outgassing, industrial processes, and biomass burning. Its primary sinks are vegetation and soils. Despite the importance of OCS in atmospheric processes, the OCS atmospheric budget is poorly determined and has high uncertainty. OCS is typically monitored using either canisters analyzed by gas chromatography or integrated atmospheric column measurements. Improved in-situ terrestrial flux and airborne measurements are required to constrain the OCS budget and further elucidate its role in stratospheric aerosol formation and as a tracer for biogenic volatile organics and photosynthesis. Los Gatos Research has developed a flight capable mid-infrared Off-Axis Integrated Cavity Output Spectroscopy (OA-ICOS) analyzer to simultaneously quantify OCS, CO2, CO, and H2O in ambient air at up to 2 Hz. The prototype was tested on diluted, certified samples and found to be precise (OCS, CO2, CO, and H2O to better than ±4 ppt, ±0.2 ppm, ±0.31 ppb, and ±3.7 ppm respectively, 1s in 1 sec) and linear (R2 > 0.9997 for all gases) over a wide dynamic range (OCS, CO2, CO, and H2O ranging from 0.2 - 70 ppb, 500 - 3000 ppm, 150 - 480 ppb, and 7000 - 21000 ppm respectively). Cross-interference measurements showed no appreciable change in measured OCS concentration with variations in CO2 (500 - 3500 ppm) or CO. We report on high altitude measurements made aboard NASA's WB-57 research aircraft. Two research flights were conducted from Houston, TX. The concentration of OCS, CO2, CO, and H2O were continuously recorded from sea level to approximately 60,000 feet. The concentration of OCS was observed to increase with altitude through the troposphere due to the

Water loss from terrestrial planets with CO{sub 2}-rich atmospheres

Energy Technology Data Exchange (ETDEWEB)

Wordsworth, R. D.; Pierrehumbert, R. T., E-mail: rwordsworth@uchicago.edu [Department of the Geophysical Sciences, University of Chicago, 60637 IL (United States)

2013-12-01

Water photolysis and hydrogen loss from the upper atmospheres of terrestrial planets is of fundamental importance to climate evolution but remains poorly understood in general. Here we present a range of calculations we performed to study the dependence of water loss rates from terrestrial planets on a range of atmospheric and external parameters. We show that CO{sub 2} can only cause significant water loss by increasing surface temperatures over a narrow range of conditions, with cooling of the middle and upper atmosphere acting as a bottleneck on escape in other circumstances. Around G-stars, efficient loss only occurs on planets with intermediate CO{sub 2} atmospheric partial pressures (0.1-1 bar) that receive a net flux close to the critical runaway greenhouse limit. Because G-star total luminosity increases with time but X-ray and ultraviolet/ultravoilet luminosity decreases, this places strong limits on water loss for planets like Earth. In contrast, for a CO{sub 2}-rich early Venus, diffusion limits on water loss are only important if clouds caused strong cooling, implying that scenarios where the planet never had surface liquid water are indeed plausible. Around M-stars, water loss is primarily a function of orbital distance, with planets that absorb less flux than ∼270 W m{sup –2} (global mean) unlikely to lose more than one Earth ocean of H{sub 2}O over their lifetimes unless they lose all their atmospheric N{sub 2}/CO{sub 2} early on. Because of the variability of H{sub 2}O delivery during accretion, our results suggest that many 'Earth-like' exoplanets in the habitable zone may have ocean-covered surfaces, stable CO{sub 2}/H{sub 2}O-rich atmospheres, and high mean surface temperatures.

State of the Carbon Cycle - Consequences of Rising Atmospheric CO2

Science.gov (United States)

Moore, D. J.; Cooley, S. R.; Alin, S. R.; Brown, M. E.; Butman, D. E.; French, N. H. F.; Johnson, Z. I.; Keppel-Aleks, G.; Lohrenz, S. E.; Ocko, I.; Shadwick, E. H.; Sutton, A. J.; Potter, C. S.; Yu, R. M. S.

2016-12-01

The rise of atmospheric CO2, largely attributable to human activity through fossil fuel emissions and land-use change, has been dampened by carbon uptake by the ocean and terrestrial biosphere. We outline the consequences of this carbon uptake as direct and indirect effects on terrestrial and oceanic systems and processes for different regions of North America and the globe. We assess the capacity of these systems to continue to act as carbon sinks. Rising CO2 has decreased seawater pH; this process of ocean acidification has impacted some marine species and altered fundamental ecosystem processes with further effects likely. In terrestrial ecosystems, increased atmospheric CO2 causes enhanced photosynthesis, net primary production, and increased water-use efficiency. Rising CO2 may change vegetation composition and carbon storage, and widespread increases in water use efficiency likely influence terrestrial hydrology and biogeochemical cycling. Consequences for human populations include changes to ecosystem services including cultural activities surrounding land use, agricultural or harvesting practices. Commercial fish stocks have been impacted and crop production yields have been changed as a result of rising CO2. Ocean and terrestrial effects are contingent on, and feedback to, global climate change. Warming and modified precipitation regimes impact a variety of ecosystem processes, and the combination of climate change and rising CO2 contributes considerable uncertainty to forecasting carbon sink capacity in the ocean and on land. Disturbance regime (fire and insects) are modified with increased temperatures. Fire frequency and intensity increase, and insect lifecycles are disrupted as temperatures move out of historical norms. Changes in disturbance patterns modulate the effects of rising CO2 depending on ecosystem type, disturbance frequency, and magnitude of events. We discuss management strategies designed to limit the rise of atmospheric CO2 and reduce

State of the Carbon Cycle - Consequences of Rising Atmospheric CO2

Science.gov (United States)

Moore, David J.; Cooley, Sarah R.; Alin, Simone R.; Brown, Molly; Butman, David E.; French, Nancy H. F.; Johnson, Zackary I.; Keppel-Aleks; Lohrenz, Steven E.; Ocko, Ilissa;

The equilibrium response to doubling atmospheric CO2

International Nuclear Information System (INIS)

Mitchell, J.F.B.

1990-01-01

The equilibrium response of climate to increased atmospheric carbon dioxide as simulated by general circulation models is assessed. Changes that are physically plausible are summarized, along with an indication of the confidence attributable to those changes. The main areas of uncertainty are highlighted. They include: equilibrium experiments with mixed-layer oceans focusing on temperature, precipitation, and soil moisture; equilibrium studies with dynamical ocean-atmosphere models; results deduced from equilibrium CO 2 experiments; and priorities for future research to improve atmosphere models

Study of the Role of Terrestrial Processes in the Carbon Cycle Based on Measurements of the Abundance and Isotopic Composition of Atmospheric CO2

Energy Technology Data Exchange (ETDEWEB)

Piper, Stephen C; Keeling, Ralph F

2012-01-03

The main objective of this project was to continue research to develop carbon cycle relationships related to the land biosphere based on remote measurements of atmospheric CO2 concentration and its isotopic ratios 13C/12C, 18O/16O, and 14C/12C. The project continued time-series observations of atmospheric carbon dioxide and isotopic composition begun by Charles D. Keeling at remote sites, including Mauna Loa, the South Pole, and eight other sites. Using models of varying complexity, the concentration and isotopic measurements were used to study long-term change in the interhemispheric gradients in CO2 and 13C/12C to assess the magnitude and evolution of the northern terrestrial carbon sink, to study the increase in amplitude of the seasonal cycle of CO2, to use isotopic data to refine constraints on large scale changes in isotopic fractionation which may be related to changes in stomatal conductance, and to motivate improvements in terrestrial carbon cycle models. The original proposal called for a continuation of the new time series of 14C measurements but subsequent descoping to meet budgetary constraints required termination of measurements in 2007.

The millennial atmospheric lifetime of anthropogenic CO{sub 2}

Energy Technology Data Exchange (ETDEWEB)

Archer, D. [University of Chicago, IL (United States). Department of the Geophysical Sciences; Brovkin, V. [Potsdam Institute for Climate Impact Research (Germany)

2008-10-15

The notion is pervasive in the climate science community and in the public at large that the climate impacts of fossil fuel CO{sub 2} release will only persist for a few centuries. This conclusion has no basis in theory or models of the atmosphere/ocean carbon cycle, which we review here. The largest fraction of the CO{sub 2} recovery will take place on time scales of centuries, as CO{sub 2} invades the ocean, but a significant fraction of the fossil fuel CO{sub 2}, ranging in published models in the literature from 20-60%, remains airborne for a thousand years or longer. Ultimate recovery takes place on time scales of hundreds of thousands of years, a geologic longevity typically associated in public perceptions with nuclear waste. The glacial/interglacial climate cycles demonstrate that ice sheets and sea level respond dramatically to millennial-timescale changes in climate forcing. There are also potential positive feedbacks in the carbon cycle, including methane hydrates in the ocean, and peat frozen in permafrost, that are most sensitive to the long tail of the fossil fuel CO{sub 2} in the atmosphere.

Atmospheric CO2 measurements with a 2-μm DIAL instrument

Science.gov (United States)

Cadiou, Erwan; Dherbecourt*, Jean-Baptiste; Gorju, Guillaume; Melkonian, Jean-Michel; Godard, Antoine; Pelon, Jacques; Raybaut, Myriam

2018-04-01

We report on ground-based atmospheric concentration measurements of carbon dioxide, using a pulsed direct detection differential absorption lidar operating at 2051 nm. The transmitter is based on a tunable parametric source emitting 10-mJ energy, 10-ns duration Fourier-limited pulses. Range resolved concentration measurements have been carried out on the aerosol back-scattered signal. Cloud signals have been used to get long range integrated-path measurements.

TransCom model simulations of hourly atmospheric CO2: Analysis of synoptic-scale variations for the period 2002-2003

NARCIS (Netherlands)

Patra, P. K.; Law, R. M.; Peters, W.; RöDenbeck, C.; Takigawa, M.; Aulagnier, C.; Baker, I.; Bergmann, D. J.; Bousquet, P.; Brandt, J.; Bruhwiler, L.; Cameron-Smith, P. J.; Christensen, J. H.; Delage, F.; Denning, A. S.; Fan, S.; Geels, C.; Houweling, S.; Imasu, R.; Karstens, U.; Kawa, S. R.; Kleist, J.; Krol, M. C.; Lin, S.-J.; Lokupitiya, R.; Maki, T.; Maksyutov, S.; Niwa, Y.; Onishi, R.; Parazoo, N.; Pieterse, G.; Rivier, L.; Satoh, M.; Serrar, S.; Taguchi, S.; Vautard, R.; Vermeulen, A. T.; Zhu, Z.

2008-01-01

The ability to reliably estimate CO2 fluxes from current in situ atmospheric CO2 measurements and future satellite CO2 measurements is dependent on transport model performance at synoptic and shorter timescales. The TransCom continuous experiment was designed to evaluate the performance of forward

An approach for verifying biogenic greenhouse gas emissions inventories with atmospheric CO2 concentration data

International Nuclear Information System (INIS)

Ogle, Stephen M; Davis, Kenneth; Lauvaux, Thomas; Miles, Natasha L; Richardson, Scott; Schuh, Andrew; Cooley, Dan; Breidt, F Jay; West, Tristram O; Heath, Linda S; Smith, James E; McCarty, Jessica L; Gurney, Kevin R; Tans, Pieter; Denning, A Scott

2015-01-01

Verifying national greenhouse gas (GHG) emissions inventories is a critical step to ensure that reported emissions data to the United Nations Framework Convention on Climate Change (UNFCCC) are accurate and representative of a country’s contribution to GHG concentrations in the atmosphere. Furthermore, verifying biogenic fluxes provides a check on estimated emissions associated with managing lands for carbon sequestration and other activities, which often have large uncertainties. We report here on the challenges and results associated with a case study using atmospheric measurements of CO 2 concentrations and inverse modeling to verify nationally-reported biogenic CO 2 emissions. The biogenic CO 2 emissions inventory was compiled for the Mid-Continent region of United States based on methods and data used by the US government for reporting to the UNFCCC, along with additional sources and sinks to produce a full carbon balance. The biogenic emissions inventory produced an estimated flux of −408 ± 136 Tg CO 2 for the entire study region, which was not statistically different from the biogenic flux of −478 ± 146 Tg CO 2 that was estimated using the atmospheric CO 2 concentration data. At sub-regional scales, the spatial density of atmospheric observations did not appear sufficient to verify emissions in general. However, a difference between the inventory and inversion results was found in one isolated area of West-central Wisconsin. This part of the region is dominated by forestlands, suggesting that further investigation may be warranted into the forest C stock or harvested wood product data from this portion of the study area. The results suggest that observations of atmospheric CO 2 concentration data and inverse modeling could be used to verify biogenic emissions, and provide more confidence in biogenic GHG emissions reporting to the UNFCCC. (letter)

A Novel Triple-Pulsed 2-micrometer Lidar for Simultaneous and Independent CO2 and H2O Column Measurement

Science.gov (United States)

Yu, Jirong; Singh, Upendra; Petros, Mulugeta; Refaat, Tamer

2015-01-01

The study of global warming needs precisely and accurately measuring greenhouse gases concentrations in the atmosphere. CO2 and H2O are important greenhouse gases that significantly contribute to the carbon cycle and global radiation budget on Earth. NRC Decadal Survey recommends a mission for Active Sensing of Carbon Dioxide (CO2) over Nights, Days and Seasons (ASCENDS). 2 micron laser is a viable IPDA transmitter to measure CO2 and H2O column density from space. The objective is to demonstrate a first airborne direct detection 2 micron IPDA lidar for CO2 and H2O measurements.

Removing traffic emissions from CO2 time series measured at a tall tower using mobile measurements and transport modeling

Science.gov (United States)

Schmidt, Andres; Rella, Chris W.; Göckede, Mathias; Hanson, Chad; Yang, Zhenlin; Law, Beverly E.

2014-11-01

In recent years, measurements of atmospheric carbon dioxide with high precision and accuracy have become increasingly important for climate change research, in particular to inform terrestrial biosphere models. Anthropogenic carbon dioxide emissions from fossil fuel burning have long been recognized to contribute a significant portion of the carbon dioxide in the atmosphere. Here, we present an approach to remove the traffic related carbon dioxide emissions from mole fractions measured at a tall tower by using the corresponding carbon monoxide measurements in combination with footprint analyses and transport modeling. This technique improves the suitability of the CO2 data to be used in inverse modeling approaches of atmosphere-biosphere exchange that do not account for non-biotic portions of CO2. In our study region in Oregon, road traffic emissions are the biggest source of anthropogenic carbon dioxide and carbon monoxide. A three-day mobile campaign covering 1700 km of roads in northwestern Oregon was performed during summer of 2012 using a laser-based Cavity Ring-Down Spectrometer. The mobile measurements incorporated different roads including main highways, urban streets, and back-roads, largely within the typical footprint of a tall CO/CO2 observation tower in Oregon's Willamette Valley. For the first time, traffic related CO:CO2 emission ratios were measured directly at the sources during an on-road campaign under a variety of different driving conditions. An average emission ratio of 7.43 (±1.80) ppb CO per ppm CO2 was obtained for the study region and applied to separate the traffic related portion of CO2 from the mole fraction time series. The road traffic related portion of the CO2 mole fractions measured at the tower site reached maximum values ranging from 9.8 to 12 ppm, depending on the height above the surface, during summer 2012.

Interannual Variability In the Atmospheric CO2 Rectification Over Boreal Forests Based On A Coupled Ecosystem-Atmosphere Model

Science.gov (United States)

Chen, B.; Chen, J. M.; Worthy, D.

2004-05-01

Ecosystem CO2 exchange and the planetary boundary layer (PBL) are correlated diurnally and seasonally. The simulation of this atmospheric rectifier effect is important in understanding the global CO2 distribution pattern. A 12-year (1990-1996, 1999-2003), continuous CO2 measurement record from Fraserdale, Ontario (located ~150 km north of Timmons), along with a coupled Vertical Diffusion Scheme (VDS) and ecosystem model (Boreal Ecosystem Productivity Simulator, BEPS), is used to investigate the interannual variability in this effect over a boreal forest region. The coupled model performed well in simulating CO2 vertical diffusion processes. Simulated annual atmospheric rectifier effects, (including seasonal and diurnal), quantified as the variation in the mean CO2 concentration from the surface to the top of the PBL, varied from 2.8 to 4.1 ppm, even though the modeled seasonal variations in the PBL depth were similar throughout the 12-year period. The differences in the interannual rectifier effect primarily resulted from changes in the biospheric CO2 uptake and heterotrophic respiration. Correlations in the year-to year variations of the CO2 rectification were found with mean annual air temperatures, simulated gross primary productivity (GPP) and heterotrophic respiration (Rh) (r2=0.5, 0.46, 0.42, respectively). A small increasing trend in the CO2 rectification was also observed. The year-to-year variation in the vertical distribution of the monthly mean CO2 mixing ratios (reflecting differences in the diurnal rectifier effect) was related to interannual climate variability, however, the seasonal rectifier effects were found to be more sensitive to climate variability than the diurnal rectifier effects.

Diurnal, synoptic and seasonal variability of atmospheric CO2 in the Paris megacity area

Science.gov (United States)

Xueref-Remy, Irène; Dieudonné, Elsa; Vuillemin, Cyrille; Lopez, Morgan; Lac, Christine; Schmidt, Martina; Delmotte, Marc; Chevallier, Frédéric; Ravetta, François; Perrussel, Olivier; Ciais, Philippe; Bréon, François-Marie; Broquet, Grégoire; Ramonet, Michel; Spain, T. Gerard; Ampe, Christophe

2018-03-01

Most of the global fossil fuel CO2 emissions arise from urbanized and industrialized areas. Bottom-up inventories quantify them but with large uncertainties. In 2010-2011, the first atmospheric in situ CO2 measurement network for Paris, the capital of France, began operating with the aim of monitoring the regional atmospheric impact of the emissions coming from this megacity. Five stations sampled air along a northeast-southwest axis that corresponds to the direction of the dominant winds. Two stations are classified as rural (Traînou - TRN; Montgé-en-Goële - MON), two are peri-urban (Gonesse - GON; Gif-sur-Yvette - GIF) and one is urban (EIF, located on top of the Eiffel Tower). In this study, we analyze the diurnal, synoptic and seasonal variability of the in situ CO2 measurements over nearly 1 year (8 August 2010-13 July 2011). We compare these datasets with remote CO2 measurements made at Mace Head (MHD) on the Atlantic coast of Ireland and support our analysis with atmospheric boundary layer height (ABLH) observations made in the center of Paris and with both modeled and observed meteorological fields. The average hourly CO2 diurnal cycles observed at the regional stations are mostly driven by the CO2 biospheric cycle, the ABLH cycle and the proximity to urban CO2 emissions. Differences of several µmol mol-1 (ppm) can be observed from one regional site to the other. The more the site is surrounded by urban sources (mostly residential and commercial heating, and traffic), the more the CO2 concentration is elevated, as is the associated variability which reflects the variability of the urban sources. Furthermore, two sites with inlets high above ground level (EIF and TRN) show a phase shift of the CO2 diurnal cycle of a few hours compared to lower sites due to a strong coupling with the boundary layer diurnal cycle. As a consequence, the existence of a CO2 vertical gradient above Paris can be inferred, whose amplitude depends on the time of the day and on

First estimates of the contribution of CaCO3 precipitation to the release of CO2 to the atmosphere during young sea ice growth

Science.gov (United States)

Geilfus, N.-X.; Carnat, G.; Dieckmann, G. S.; Halden, N.; Nehrke, G.; Papakyriakou, T.; Tison, J.-L.; Delille, B.

2013-01-01

report measurements of pH, total alkalinity, air-ice CO2 fluxes (chamber method), and CaCO3 content of frost flowers (FF) and thin landfast sea ice. As the temperature decreases, concentration of solutes in the brine skim increases. Along this gradual concentration process, some salts reach their solubility threshold and start precipitating. The precipitation of ikaite (CaCO3.6H2O) was confirmed in the FF and throughout the ice by Raman spectroscopy and X-ray analysis. The amount of ikaite precipitated was estimated to be 25 µmol kg-1 melted FF, in the FF and is shown to decrease from 19 to 15 µmol kg-1 melted ice in the upper part and at the bottom of the ice, respectively. CO2 release due to precipitation of CaCO3 is estimated to be 50 µmol kg-1 melted samples. The dissolved inorganic carbon (DIC) normalized to a salinity of 10 exhibits significant depletion in the upper layer of the ice and in the FF. This DIC loss is estimated to be 2069 µmol kg-1 melted sample and corresponds to a CO2 release from the ice to the atmosphere ranging from 20 to 40 mmol m-2 d-1. This estimate is consistent with flux measurements of air-ice CO2 exchange. Our measurements confirm previous laboratory findings that growing young sea ice acts as a source of CO2 to the atmosphere. CaCO3 precipitation during early ice growth appears to promote the release of CO2 to the atmosphere; however, its contribution to the overall release by newly formed ice is most likely minor.

Oxygen isotope anomaly in tropospheric CO2 and implications for CO2 residence time in the atmosphere and gross primary productivity.

Science.gov (United States)

Liang, Mao-Chang; Mahata, Sasadhar; Laskar, Amzad H; Thiemens, Mark H; Newman, Sally

2017-10-13

The abundance variations of near surface atmospheric CO 2 isotopologues (primarily 16 O 12 C 16 O, 16 O 13 C 16 O, 17 O 12 C 16 O, and 18 O 12 C 16 O) represent an integrated signal from anthropogenic/biogeochemical processes, including fossil fuel burning, biospheric photosynthesis and respiration, hydrospheric isotope exchange with water, and stratospheric photochemistry. Oxygen isotopes, in particular, are affected by the carbon and water cycles. Being a useful tracer that directly probes governing processes in CO 2 biogeochemical cycles, Δ 17 O (=ln(1 + δ 17 O) - 0.516 × ln(1 + δ 18 O)) provides an alternative constraint on the strengths of the associated cycles involving CO 2 . Here, we analyze Δ 17 O data from four places (Taipei, Taiwan; South China Sea; La Jolla, United States; Jerusalem, Israel) in the northern hemisphere (with a total of 455 measurements) and find a rather narrow range (0.326 ± 0.005‰). A conservative estimate places a lower limit of 345 ± 70 PgC year -1 on the cycling flux between the terrestrial biosphere and atmosphere and infers a residence time of CO 2 of 1.9 ± 0.3 years (upper limit) in the atmosphere. A Monte Carlo simulation that takes various plant uptake scenarios into account yields a terrestrial gross primary productivity of 120 ± 30 PgC year -1 and soil invasion of 110 ± 30 PgC year -1 , providing a quantitative assessment utilizing the oxygen isotope anomaly for quantifying CO 2 cycling.

Impacts of elevated atmospheric CO2 on forest trees and forest ecosystems: knowledge gaps

International Nuclear Information System (INIS)

Karnosky, D.F.

2003-06-01

Atmospheric CO 2 is rising rapidly, and options for slowing the CO 2 rise are politically charged as they largely require reductions in industrial CO 2 emissions for most developed countries. As forests cover some 43% of the Earth's surface, account for some 70% of terrestrial net primary production (NPP), and are being bartered for carbon mitigation, it is critically important that we continue to reduce the uncertainties about the impacts of elevated atmospheric CO 2 on forest tree growth, productivity, and forest ecosystem function. In this paper, 1 review knowledge gaps and research needs on the effects of elevated atmospheric CO 2 on forest above- and below-ground growth and productivity, carbon sequestration, nutrient cycling, water relations, wood quality, phonology, community dynamics and biodiversity, antioxidants and stress tolerance, interactions with air pollutants, heterotrophic interactions, and ecosystem functioning. Finally, 1 discuss research needs regarding modelling of the impacts of elevated atmospheric CO 2 on forests. Even though there has been a tremendous amount of research done with elevated CO 2 and forest trees, it remains difficult to predict future forest growth and productivity under elevated atmospheric CO 2 . Likewise, it is not easy to predict how forest ecosystem processes will respond to enriched CO 2 . The more we study the impacts of increasing CO 2 , the more we realize that tree and forest responses are yet largely uncertain due to differences in responsiveness by species, genotype, and functional group, and the complex interactions of elevated atmospheric CO 2 with soil fertility, drought, pests, and co-occurring atmospheric pollutants such as nitrogen deposition and O 3 . Furthermore, it is impossible to predict ecosystem-level responses based on short-term studies of young trees grown without interacting stresses and in small spaces without the element of competition. Long-term studies using free-air CO 2 enrichment (FACE

Fast Atmosphere-Ocean Model Runs with Large Changes in CO2

Science.gov (United States)

Russell, Gary L.; Lacis, Andrew A.; Rind, David H.; Colose, Christopher; Opstbaum, Roger F.

2013-01-01

How does climate sensitivity vary with the magnitude of climate forcing? This question was investigated with the use of a modified coupled atmosphere-ocean model, whose stability was improved so that the model would accommodate large radiative forcings yet be fast enough to reach rapid equilibrium. Experiments were performed in which atmospheric CO2 was multiplied by powers of 2, from 1/64 to 256 times the 1950 value. From 8 to 32 times, the 1950 CO2, climate sensitivity for doubling CO2 reaches 8 C due to increases in water vapor absorption and cloud top height and to reductions in low level cloud cover. As CO2 amount increases further, sensitivity drops as cloud cover and planetary albedo stabilize. No water vapor-induced runaway greenhouse caused by increased CO2 was found for the range of CO2 examined. With CO2 at or below 1/8 of the 1950 value, runaway sea ice does occur as the planet cascades to a snowball Earth climate with fully ice covered oceans and global mean surface temperatures near 30 C.

On the CO2 exchange between the atmosphere and the biosphere: the role of synoptic and mesoscale processes

International Nuclear Information System (INIS)

Chan, Douglas; Higuchi, Kaz; Shashkov, Alexander; Worthy, Douglas; Liu, Jane; Chen Jing; Yuen Chiu Wai

2004-01-01

Estimating global carbon fluxes by inverting atmospheric CO 2 through the use of atmospheric transport models has shown the importance of the covariance between biospheric fluxes and atmospheric transport on the carbon budget. This covariance or coupling occurs on many time scales. This study examines the coupling of the biosphere and the atmosphere on the meso- and synoptic scales using a coupled atmosphere-biosphere regional model covering Canada. The results are compared with surface and light aircraft measurement campaigns at two boreal forest sites in Canada. Associated with cold and warm frontal features, the model results showed that the biospheric fluxes are strongly coupled to the atmosphere through radiative forcing. The presence of cloud near frontal regions usually results in reduced photosynthetic uptake, producing CO 2 concentration gradients across the frontal regions on the order of 10 parts per million (ppm). Away from the frontal region, the biosphere is coupled to the mesoscale variations in similar ways, resulting in mesoscale variations in CO 2 concentrations of about 5 ppm. The CO 2 field is also coupled strongly to the atmospheric dynamics. In the presence of frontal circulation, the CO 2 near the surface can be transported to the mid to upper troposphere. Mesoscale circulation also plays a significant part in transporting the CO 2 from the planetary boundary layer (PBL) to the mid-troposphere. In the absence of significant mesoscale or synoptic scale circulation, the CO 2 in the PBL has minimal exchange with the free troposphere, leading to strong gradients across the top of the PBL. We speculate that the ubiquity of the common synoptic and mesoscale processes in the atmosphere may contribute significantly to the rectifier effect and hence CO 2 inversion calculations

Atmospheric measurements of ratios between CO2 and co-emitted species from traffic: a tunnel study in the Paris mega-city

International Nuclear Information System (INIS)

Ammoura, L.; Xueref-Remy, I.; Gros, V.; Baudic, A.; Bonsang, B.; Bonnaire, N.; Sciare, J.; Chevallier, F.; Petit, J.E.; Perrussel, O.

2014-01-01

Measurements of CO 2 , CO, NO x and selected Volatile Organic Compounds (VOCs) mole fractions were performed continuously during a 10-day period in the Guy Moquet tunnel in Thiais, a peri-urban area about 15 km south of the centre of Paris, between 28 September and 8 October 2012. This data set is used here to identify the characteristics of traffic-emitted CO 2 by evaluating its ratios to co-emitted species for the first time in the Paris region. High coefficients of determination (r 2 ≥ 0.7) are observed between CO 2 and certain compounds that are characteristic of the traffic source (CO, NO x , benzene, xylenes and acetylene). Weak correlations (r 2 ≤ 0.2) are found with species such as propane, n- butane and i-butane that are associated with fuel evaporation, an insignificant source for CO 2 . To better characterise the traffic signal we focus only on species that are well correlated with CO 2 and on rush-hour periods characterised by the highest traffic-related mole fractions. From those mole fractions we remove the nighttime-average weekday mole fraction obtained for each species that we infer to be the most appropriate background signal for our study. Then we calculate observed Δspecies / ΔCO 2 ratios, which we compare with the ones provided by the 2010 bottom-up high-resolved regional emission inventory from Airparif (the association in charge of monitoring the air quality in ile-de-France), focusing on local emission data for the specific road of the tunnel. We find an excellent agreement (2 %) between the local inventory emission CO/CO 2 ratio and our observed ΔCO/ΔCO 2 ratio. Former tunnel experiments carried out elsewhere in the world provided observed ΔCO/ΔCO 2 ratios that differ from 49 to 592% to ours. This variability can be related to technological improvement of vehicles, differences in driving conditions, and fleet composition. We also find a satisfactory agreement with the Airparif inventory for n-propylbenzene, n-pentane and xylenes

Reconciling the Differences between the Measurements of CO2 Isotopes by the Phoenix and MSL Landers

Science.gov (United States)

Niles, P. B.; Mahaffy, P. R.; Atreya, S.; Pavlov, A. A.; Trainer, M.; Webster, C. R.; Wong, M.

2014-01-01

Precise stable isotope measurements of the CO2 in the martian atmosphere have the potential to provide important constraints for our understanding of the history of volatiles, the carbon cycle, current atmospheric processes, and the degree of water/rock interaction on Mars. There have been several different measurements by landers and Earth based systems performed in recent years that have not been in agreement. In particular, measurements of the isotopic composition of martian atmospheric CO2 by the Thermal and Evolved Gas Analyzer (TEGA) instrument on the Mars Phoenix Lander and the Sample Analysis at Mars (SAM) instrument on the Mars Science Laboratory (MSL) are in stark disagreement. This work attempts to use measurements of mass 45 and mass 46 of martian atmospheric CO2 by the SAM and TEGA instruments to search for agreement as a first step towards reaching a consensus measurement that might be supported by data from both instruments.

A new set-up for simultaneous high-precision measurements of CO2, δ13C-CO2 and δ18O-CO2 on small ice core samples

Science.gov (United States)

Jenk, Theo Manuel; Rubino, Mauro; Etheridge, David; Ciobanu, Viorela Gabriela; Blunier, Thomas

2016-08-01

Palaeoatmospheric records of carbon dioxide and its stable carbon isotope composition (δ13C) obtained from polar ice cores provide important constraints on the natural variability of the carbon cycle. However, the measurements are both analytically challenging and time-consuming; thus only data exist from a limited number of sampling sites and time periods. Additional analytical resources with high analytical precision and throughput are thus desirable to extend the existing datasets. Moreover, consistent measurements derived by independent laboratories and a variety of analytical systems help to further increase confidence in the global CO2 palaeo-reconstructions. Here, we describe our new set-up for simultaneous measurements of atmospheric CO2 mixing ratios and atmospheric δ13C and δ18O-CO2 in air extracted from ice core samples. The centrepiece of the system is a newly designed needle cracker for the mechanical release of air entrapped in ice core samples of 8-13 g operated at -45 °C. The small sample size allows for high resolution and replicate sampling schemes. In our method, CO2 is cryogenically and chromatographically separated from the bulk air and its isotopic composition subsequently determined by continuous flow isotope ratio mass spectrometry (IRMS). In combination with thermal conductivity measurement of the bulk air, the CO2 mixing ratio is calculated. The analytical precision determined from standard air sample measurements over ice is ±1.9 ppm for CO2 and ±0.09 ‰ for δ13C. In a laboratory intercomparison study with CSIRO (Aspendale, Australia), good agreement between CO2 and δ13C results is found for Law Dome ice core samples. Replicate analysis of these samples resulted in a pooled standard deviation of 2.0 ppm for CO2 and 0.11 ‰ for δ13C. These numbers are good, though they are rather conservative estimates of the overall analytical precision achieved for single ice sample measurements. Facilitated by the small sample requirement

Late-glacial atmospheric CO{sub 2} reconstructions from western Norway using fossil leaves

Energy Technology Data Exchange (ETDEWEB)

Birks, H H; Birks, H J.B. [Sheffield Univ. (United Kingdom). Dept. of Animal and Plant Sciences; Beerling, D J; Woodward, F I [Bergen Univ. (Norway). Botanical Inst.

1996-12-31

Analyses of air bubbles trapped in Antarctic ice-cores have shown that atmospheric CO{sub 2} concentrations are 180-200 ppmv during glacial periods, and ca. 280 ppmv during interglacials, including the Holocene. The change from glacial to Holocene concentrations occurred steadily over ca. 5000 years, slightly lagging the temperature increase inferred from {delta}{sup 18}. Antarctic ice cores lack fine time resolution over the late-glacial/early Holocene period 12-9000 {sup 14}C yr BP, that includes the Younger Dryas cold oscillation. The stomatal density on leaves is inversely proportional to the concentration of atmospheric CO{sub 2}. A late glacial sequence at Kraakenes, western Norway, contains well-preserved Salix herbacea (dwarf willow) leaves, dated from 11700-9600 {sup 14}C yr BP. If the stomatal density is measured on the fossil leaves, a calibration derived from the relationship of stomatal density of modern material of the same species to known CO{sub 2} concentrations can be used to reconstruct CO{sub 2} concentrations of the past. Because of the decadal time-resolution available at Kraakenes through the late-glacial and early Holocene, a detailed record of CO{sub 2} concentrations can be reconstructed over this period, that will complement the ice core record. (author)

Late-glacial atmospheric CO{sub 2} reconstructions from western Norway using fossil leaves

Energy Technology Data Exchange (ETDEWEB)

Birks, H.H.; Birks, H.J.B. [Sheffield Univ. (United Kingdom). Dept. of Animal and Plant Sciences; Beerling, D.J.; Woodward, F.I. [Bergen Univ. (Norway). Botanical Inst.

1995-12-31

Analyses of air bubbles trapped in Antarctic ice-cores have shown that atmospheric CO{sub 2} concentrations are 180-200 ppmv during glacial periods, and ca. 280 ppmv during interglacials, including the Holocene. The change from glacial to Holocene concentrations occurred steadily over ca. 5000 years, slightly lagging the temperature increase inferred from {delta}{sup 18}. Antarctic ice cores lack fine time resolution over the late-glacial/early Holocene period 12-9000 {sup 14}C yr BP, that includes the Younger Dryas cold oscillation. The stomatal density on leaves is inversely proportional to the concentration of atmospheric CO{sub 2}. A late glacial sequence at Kraakenes, western Norway, contains well-preserved Salix herbacea (dwarf willow) leaves, dated from 11700-9600 {sup 14}C yr BP. If the stomatal density is measured on the fossil leaves, a calibration derived from the relationship of stomatal density of modern material of the same species to known CO{sub 2} concentrations can be used to reconstruct CO{sub 2} concentrations of the past. Because of the decadal time-resolution available at Kraakenes through the late-glacial and early Holocene, a detailed record of CO{sub 2} concentrations can be reconstructed over this period, that will complement the ice core record. (author)

Impact of atmospheric and terrestrial CO2 feedbacks on fertilization-induced marine carbon uptake

Science.gov (United States)

Oschlies, A.

2009-08-01

The sensitivity of oceanic CO2 uptake to alterations in the marine biological carbon pump, such as brought about by natural or purposeful ocean fertilization, has repeatedly been investigated by studies employing numerical biogeochemical ocean models. It is shown here that the results of such ocean-centered studies are very sensitive to the assumption made about the response of the carbon reservoirs on the atmospheric side of the sea surface. Assumptions made include prescribed atmospheric pCO2, an interactive atmospheric CO2 pool exchanging carbon with the ocean but not with the terrestrial biosphere, and an interactive atmosphere that exchanges carbon with both oceanic and terrestrial carbon pools. The impact of these assumptions on simulated annual to millennial oceanic carbon uptake is investigated for a hypothetical increase in the C:N ratio of the biological pump and for an idealized enhancement of phytoplankton growth. Compared to simulations with interactive atmosphere, using prescribed atmospheric pCO2 overestimates the sensitivity of the oceanic CO2 uptake to changes in the biological pump, by about 2%, 25%, 100%, and >500% on annual, decadal, centennial, and millennial timescales, respectively. The smaller efficiency of the oceanic carbon uptake under an interactive atmosphere is due to the back flux of CO2 that occurs when atmospheric CO2 is reduced. Adding an interactive terrestrial carbon pool to the atmosphere-ocean model system has a small effect on annual timescales, but increases the simulated fertilization-induced oceanic carbon uptake by about 4%, 50%, and 100% on decadal, centennial, and millennial timescales, respectively, for pCO2 sensitivities of the terrestrial carbon storage in the middle range of the C4MIP models (Friedlingstein et al., 2006). For such sensitivities, a substantial fraction of oceanic carbon uptake induced by natural or purposeful ocean fertilization originates, on timescales longer than decades, not from the atmosphere

Greenhouse gases regional fluxes estimated from atmospheric measurements

International Nuclear Information System (INIS)

Messager, C.

2007-07-01

build up a new system to measure continuously CO 2 (or CO), CH 4 , N 2 O and SF 6 mixing ratios. It is based on a commercial gas chromatograph (Agilent 6890N) which have been modified to reach better precision. Reproducibility computed with a target gas on a 24 hours time step gives: 0.06 ppm for CO 2 , 1.4 ppb for CO, 0.7 ppb for CH 4 , 0.2 ppb for N 2 O and 0.05 ppt for SF 6 . The instrument's run is fully automated, an air sample analysis takes about 5 minutes. In July 2006, I install instrumentation on a telecommunication tall tower (200 m) situated near Orleans forest in Trainou, to monitor continuously greenhouse gases (CO 2 , CH 4 , N 2 O, SF 6 ), atmospheric tracers (CO, Radon-222) and meteorological parameters. Intake lines were installed at 3 levels (50, 100 and 180 m) and allow us to sample air masses along the vertical. Continuous measurement started in January 2007. I used Mace Head (Ireland) and Gif-sur-Yvette continuous measurements to estimate major greenhouse gases emission fluxes at regional scale. To make the link between atmospheric measurements and surface fluxes, we need to quantify dilution due to atmospheric transport. I used Radon-222 as tracer (radon tracer method) and planetary boundary layer heights estimates from ECMWF model (boundary layer budget method) to parameterize atmospheric transport. In both cases I compared results to available emission inventories. (author)

Airborne Measurements of CO2 Column Concentration and Range Using a Pulsed Direct-Detection IPDA Lidar

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Abshire, James B.; Ramanathan, Anand; Riris, Haris; Mao, Jianping; Allan, Graham R.; Hasselbrack, William E.; Weaver, Clark J.; Browell, Edward V.

2013-01-01

We have previously demonstrated a pulsed direct detection IPDA lidar to measure range and the column concentration of atmospheric CO2. The lidar measures the atmospheric backscatter profiles and samples the shape of the 1,572.33 nm CO2 absorption line. We participated in the ASCENDS science flights on the NASA DC-8 aircraft during August 2011 and report here lidar measurements made on four flights over a variety of surface and cloud conditions near the US. These included over a stratus cloud deck over the Pacific Ocean, to a dry lake bed surrounded by mountains in Nevada, to a desert area with a coal-fired power plant, and from the Rocky Mountains to Iowa, with segments with both cumulus and cirrus clouds. Most flights were to altitudes >12 km and had 5-6 altitude steps. Analyses show the retrievals of lidar range, CO2 column absorption, and CO2 mixing ratio worked well when measuring over topography with rapidly changing height and reflectivity, through thin clouds, between cumulus clouds, and to stratus cloud tops. The retrievals shows the decrease in column CO2 due to growing vegetation when flying over Iowa cropland as well as a sudden increase in CO2 concentration near a coal-fired power plant. For regions where the CO2 concentration was relatively constant, the measured CO2 absorption lineshape (averaged for 50 s) matched the predicted shapes to better than 1% RMS error. For 10 s averaging, the scatter in the retrievals was typically 2-3 ppm and was limited by the received signal photon count. Retrievals were made using atmospheric parameters from both an atmospheric model and from in situ temperature and pressure from the aircraft. The retrievals had no free parameters and did not use empirical adjustments, and >70% of the measurements passed screening and were used in analysis. The differences between the lidar-measured retrievals and in situ measured average CO2 column concentrations were 6 km.

The persistent and pernicious myth of the early CO2-N2 atmospheres of terrestrial planets

Science.gov (United States)

Shaw, G. H.

2009-12-01

The accepted model for early atmospheres of terrestrial planets has settled on a CO2-N2 composition. Unfortunately, while it is largely based on a brilliant geological analysis by Rubey, there is no compelling evidence whatsoever for such a composition as the first “permanent” atmosphere for Earth or any other planet. In fact, geological discoveries of the past 50+ years reveal several problems with a CO2-N2 atmosphere, some of which Rubey recognized in his own analysis. He clearly addressed the problem of timing of degassing, concluding that early massive degassing of CO2 would produce readily observed and profound effects, which are not evident. Modeling and constraints on the timing of planetary accretion and core formation indicate massive early degassing. If early degassing emitted CO2-N2, the effects are concealed. Plate tectonic recycling is not a solution, as conditions would have persisted beyond the time of the earliest rocks, which do not show the effects. Attempts to return degassed CO2 to the mantle are not only ad hoc, but inconsistent with early thermal structure of the Earth. Second, production of prebiotic organic compounds from a CO2-N2 atmosphere has been a nagging problem. At best this has been addressed by invoking hydrogen production from the mantle to provide reducing capacity. While hydrogen may be emitted in volcanic eruptions, it is exceedingly difficult to imagine this process generating enough organics to yield high concentrations in a global ocean. The recent fashion of invoking organic synthesis at deep-sea vents suffers from the same problem: how to achieve sufficient concentrations of organics in a global ocean by abiotic synthesis when hydrothermal activity stirs the solution and carries the prebiotic products off to great dilution? Suggesting life began at deep-sea vents, and continues to carry on chemosynthesis there, begs the question. Unless you get high enough concentrations of prebiotics by abiotic processes, you simply

Response of Tundra Ecosystems to Elevated Atmospheric CO{sub 2}

Energy Technology Data Exchange (ETDEWEB)

Oechel, Walter C.

1990-09-05

OAK B188 Response of Tundra Ecosystems to Elevated Atmospheric CO{sub 2}. Atmospheric CO{sub 2} is expected to double by the end of the next century. Global mean increases in surface air temperature of 1.5-4.5 C are anticipated with larger increases towards the poles predicted. Changes in CO{sub 2} levels and temperature could have major impacts on ecosystem functioning, including primary productivity, species composition, plant-animal interactions, and carbon storage. Until recently, there has been little direct information on the impact of changes in CO{sub 2} and temperature on native ecosystems. The study described here was undertaken to evaluate the effects of a 50 and 100% increase in atmospheric CO{sub 2}, and a 100% increase in atmospheric CO{sub 2} coupled with a 4 C summer air temperature rise on the structure and function of an arctic tussock tundra ecosystem. The arctic contains large stores of carbon as soil organic matter, much frozen in permafrost and currently not reactive or available for oxidation and release into the atmosphere. About 10-27% of the world's terrestrial carbon occurs in arctic and boreal regions, and carbon is accumulating in these regions at the rate of 0.19 GT y{sup -1}. Mean temperature increases of 11 C and summer temperature increases of 4 C have been suggested. Mean July temperatures on the arctic coastal plain and arctic foothills regions are 4-12 C, and mean annual temperatures are -7 to -13 C (Haugen, 1982). The projected temperature increases represent a substantial elevation above current temperatures which will have major impacts on physical processes such as permafrost development and development of the active layer, and on biological and ecosystem processes such as primary productivity, carbon storage, and species composition. Extreme nutrient and temperature limitation of this ecosystem raised questions of the responsiveness of arctic systems to elevated CO{sub 2}. Complex ecosystem interactions with the effects

Is there a decrease in the sink of atmospheric CO2 in the Nordic seas?

International Nuclear Information System (INIS)

Olsen, Are; Anderson, Leif G.

2002-01-01

It is well known that the seas off Norway sink a lot of carbon dioxide from the atmosphere, mainly because of the large heat loss from the sea in the area, which makes CO 2 more soluble in the water. Whether this sink has increased after the industrial revolution and thereby contributes to slowing down the increase of atmospheric CO 2 is uncertain. That is, it is uncertain whether there is a sink of anthropogenic CO 2 . There are indications that the opposite is true, that the sink of CO 2 in this area has slowed down along with the rise in the concentration of atmospheric CO 2 . Storing of anthropogenic CO 2 , however, takes place at higher latitudes where deep-water formation occurs, such as in the Nordic seas, where water that is saturated with anthropogenic CO 2 is transported down in the deep sea and becomes shielded from the atmosphere. Model calculations show that increased CO 2 in the atmosphere will reduce the sink of this gas in the Nordic seas. This conclusion is supported by observations from the Barents Sea

The Influence of CO2 Admixtures on the Product Composition in a Nitrogen-Methane Atmospheric Glow Discharge Used as a Prebiotic Atmosphere Mimic.

Science.gov (United States)

Mazankova, V; Torokova, L; Krcma, F; Mason, N J; Matejcik, S

2016-11-01

This work extends our previous experimental studies of the chemistry of Titan's atmosphere by atmospheric glow discharge. The Titan's atmosphere seems to be similarly to early Earth atmospheric composition. The exploration of Titan atmosphere was initiated by the exciting results of the Cassini-Huygens mission and obtained results increased the interest about prebiotic atmospheres. Present work is devoted to the role of CO 2 in the prebiotic atmosphere chemistry. Most of the laboratory studies of such atmosphere were focused on the chemistry of N 2  + CH 4 mixtures. The present work is devoted to the study of the oxygenated volatile species in prebiotic atmosphere, specifically CO 2 reactivity. CO 2 was introduced to the standard N 2  + CH 4 mixture at different mixing ratio up to 5 % CH 4 and 3 % CO 2 . The reaction products were characterized by FTIR spectroscopy. This work shows that CO 2 modifies the composition of the gas phase with the detection of oxygenated compounds: CO and others oxides. There is a strong influence of CO 2 on increasing concentration other products as cyanide (HCN) and ammonia (NH 3 ).

Sensitivity Analysis for Atmospheric Infrared Sounder (AIRS) CO2 Retrieval

Science.gov (United States)

Gat, Ilana

2012-01-01

The Atmospheric Infrared Sounder (AIRS) is a thermal infrared sensor able to retrieve the daily atmospheric state globally for clear as well as partially cloudy field-of-views. The AIRS spectrometer has 2378 channels sensing from 15.4 micrometers to 3.7 micrometers, of which a small subset in the 15 micrometers region has been selected, to date, for CO2 retrieval. To improve upon the current retrieval method, we extended the retrieval calculations to include a prior estimate component and developed a channel ranking system to optimize the channels and number of channels used. The channel ranking system uses a mathematical formalism to rapidly process and assess the retrieval potential of large numbers of channels. Implementing this system, we identifed a larger optimized subset of AIRS channels that can decrease retrieval errors and minimize the overall sensitivity to other iridescent contributors, such as water vapor, ozone, and atmospheric temperature. This methodology selects channels globally by accounting for the latitudinal, longitudinal, and seasonal dependencies of the subset. The new methodology increases accuracy in AIRS CO2 as well as other retrievals and enables the extension of retrieved CO2 vertical profiles to altitudes ranging from the lower troposphere to upper stratosphere. The extended retrieval method for CO2 vertical profile estimation using a maximum-likelihood estimation method. We use model data to demonstrate the beneficial impact of the extended retrieval method using the new channel ranking system on CO2 retrieval.

The extraction of CO2 from the atmosphere

International Nuclear Information System (INIS)

Hauet, Jean-Pierre

2014-01-01

After having indicated some methods which are considered as ridiculous, hazardous or ethically questionable, the author first presents of method of extraction of CO 2 from the atmosphere developed by a research team of the University of Calgary and applied by the Carbon Engineering Company. According to this concept, ambient air is circulated through an air-contactor in which air leaves its CO 2 to a potassium hydroxide flow which transforms into potassium carbonate. This hydroxide is then re-generated by exchange with calcium hydroxide. The thus formed calcium carbonate is finally thermally decomposed to release CO 2 . He also presents the BECCS (Bio-energy with carbon capture and storage) which has been put forward by the IPCC, evokes the cost of the extracted ton of CO 2 and the arguments of the opponents to this method

Development of Double and Triple-Pulsed 2-micron IPDA Lidars for Column CO2 Measurements

Science.gov (United States)

Singh, Upendra N.; Yu, Jirong; Petros, Mulugeta; Refaat, Tamer F.; Remus, Ruben G.; Reithmaier, Karl

2015-01-01

Carbon dioxide (CO2) is an important greenhouse gas that significantly contributes to the carbon cycle and globalradiation budget on Earth. CO2 role on Earth’s climate is complicated due to different interactions with various climatecomponents that include the atmosphere, the biosphere and the hydrosphere. Although extensive worldwide efforts formonitoring atmospheric CO2 through various techniques, including in-situ and passive sensors, are taking place highuncertainties exist in quantifying CO2 sources and sinks. These uncertainties are mainly due to insufficient spatial andtemporal mapping of the gas. Therefore it is required to have more rapid and accurate CO2 monitoring with higheruniform coverage and higher resolution. CO2 DIAL operating in the 2-µm band offer better near-surface CO2measurement sensitivity due to the intrinsically stronger absorption lines. For more than 15 years, NASA LangleyResearch Center (LaRC) contributed in developing several 2-?m CO2 DIAL systems and technologies. This paperfocuses on the current development of the airborne double-pulsed and triple-pulsed 2-?m CO2 integrated pathdifferential absorption (IPDA) lidar system at NASA LaRC. This includes the IPDA system development andintegration. Results from ground and airborne CO2 IPDA testing will be presented. The potential of scaling suchtechnology to a space mission will be addressed.

Biomass burial and storage to reduce atmospheric CO2

Science.gov (United States)

Zeng, N.

2012-04-01

To mitigate global climate change, a portfolio of strategies will be needed to keep the atmospheric CO2 concentration below a dangerous level. Here a carbon sequestration strategy is proposed in which certain dead or live trees are harvested via collection or selective cutting, then buried in trenches or stowed away in above-ground shelters. The largely anaerobic condition under a sufficiently thick layer of soil will prevent the decomposition of the buried wood. Because a large flux of CO2 is constantly being assimilated into the world's forests via photosynthesis, cutting off its return pathway to the atmosphere forms an effective carbon sink. It is estimated that a theoretical carbon sequestration potential for wood burial is 10 ± 5 GtC/y, but probably 1-3 GtC/y can be realized in practice. Burying wood has other benefits including minimizing CO2 source from deforestation, extending the lifetime of reforestation carbon sink, and reducing fire danger. There are possible environmental impacts such as nutrient lock-up which nevertheless appears manageable, but other environmental concerns and factors will likely set a limit so that only part of the full potential can be realized. Based on data from forest industry, the cost for wood burial is estimated to be 14/tCO2 (50/tC), lower than the typical cost for power plant CO2 capture with geological storage. The low cost for carbon sequestration with wood burial is possible because the technique uses the natural process of photosynthesis to remove carbon from the atmosphere. The technique is low tech, distributed, safe, and can be stopped at any time, thus an attractive option for large-scale implementation in a world-wide carbon market.

Evolutionary History of Atmospheric CO2 during the Late Cenozoic from Fossilized Metasequoia Needles.

Directory of Open Access Journals (Sweden)

Yuqing Wang

Full Text Available The change in ancient atmospheric CO2 concentrations provides important clues for understanding the relationship between the atmospheric CO2 concentration and global temperature. However, the lack of CO2 evolution curves estimated from a single terrestrial proxy prevents the understanding of climatic and environmental impacts due to variations in data. Thus, based on the stomatal index of fossilized Metasequoia needles, we reconstructed a history of atmospheric CO2 concentrations from middle Miocene to late Early Pleistocene when the climate changed dramatically. According to this research, atmospheric CO2 concentration was stabile around 330-350 ppmv in the middle and late Miocene, then it decreased to 278-284 ppmv during the Late Pliocene and to 277-279 ppmv during the Early Pleistocene, which was almost the same range as in preindustrial time. According to former research, this is a time when global temperature decreased sharply. Our results also indicated that from middle Miocene to Pleistocene, global CO2 level decreased by more than 50 ppmv, which may suggest that CO2 decrease and temperature decrease are coupled.

Evolutionary History of Atmospheric CO2 during the Late Cenozoic from Fossilized Metasequoia Needles.

Science.gov (United States)

Wang, Yuqing; Momohara, Arata; Wang, Li; Lebreton-Anberrée, Julie; Zhou, Zhekun

2015-01-01

The change in ancient atmospheric CO2 concentrations provides important clues for understanding the relationship between the atmospheric CO2 concentration and global temperature. However, the lack of CO2 evolution curves estimated from a single terrestrial proxy prevents the understanding of climatic and environmental impacts due to variations in data. Thus, based on the stomatal index of fossilized Metasequoia needles, we reconstructed a history of atmospheric CO2 concentrations from middle Miocene to late Early Pleistocene when the climate changed dramatically. According to this research, atmospheric CO2 concentration was stabile around 330-350 ppmv in the middle and late Miocene, then it decreased to 278-284 ppmv during the Late Pliocene and to 277-279 ppmv during the Early Pleistocene, which was almost the same range as in preindustrial time. According to former research, this is a time when global temperature decreased sharply. Our results also indicated that from middle Miocene to Pleistocene, global CO2 level decreased by more than 50 ppmv, which may suggest that CO2 decrease and temperature decrease are coupled.

Initial Results of an Intercomparison of AMS-Based Atmospheric 14CO2 Measurements

NARCIS (Netherlands)

Miller, John; Lehman, Scott; Wolak, Chad; Turnbull, Jocelyn; Dunn, Gregory; Graven, Heather; Keeling, Ralph; Meijer, Harro A. J.; Aerts-Bijma, Anita Th; Palstra, Sanne W. L.; Smith, Andrew M.; Allison, Colin; Southon, John; Xu, Xiaomei; Nakazawa, Takakiyo; Aoki, Shuji; Nakamura, Toshio; Guilderson, Thomas; LaFranchi, Brian; Mukai, Hitoshi; Terao, Yukio; Uchida, Masao; Kondo, Miyuki

2013-01-01

This article presents results from the first 3 rounds of an international intercomparison of measurements of Delta(CO2)-C-14 in liter-scale samples of whole air by groups using accelerator mass spectrometry (AMS). The ultimate goal of the intercomparison is to allow the merging of Delta(CO2)-C-14

Accumulation of fossil CO/sub 2/ in the atmosphere and the sea

Energy Technology Data Exchange (ETDEWEB)

Fairhall, A W

1973-09-07

A model is presented which accounts quantitatively for the buildup of fossil CO/sub 2/ in the atmosphere. The model also predicts something not previously recognized: a significant uptake of fossil CO/sub 2/ by the sea. The sea is presently supersaturated with respect to aragonite and calcite, which calcareous organisms form in building their shells. Should the sea become unsaturated in CaCO/sub 3/ the shells of these organisms would tend to dissolve, as would the ocean's coral reefs. One test of the model would be afforded by careful monitoring of total CO/sub 2/ levels in the mixed layer over the next few years. The model predicts an increase in the mixed layer of about 1.4 per cent in the next decade. Because this is about double the accuracy of the present methods for measuring total CO/sub 2/ in seawater, this trend, if present, should be detectable within 3 to 5 years. (MFB)

Wine ethanol C-14 as a tracer for fossil fuel CO2 emissions in Europe : Measurements and model comparison

NARCIS (Netherlands)

Palstra, Sanne W. L.; Karstens, Ute; Streurman, Harm-Jan; Meijer, Harro A. J.

2008-01-01

C-14 (radiocarbon) in atmospheric CO2 is the most direct tracer for the presence of fossil-fuel-derived CO2 (CO2-ff). We demonstrate the C-14 measurement of wine ethanol as a way to determine the relative regional atmospheric CO2-ff concentration compared to a background site ("regional CO2-ff

Diurnal, synoptic and seasonal variability of atmospheric CO2 in the Paris megacity area

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I. Xueref-Remy

2018-03-01

Full Text Available Most of the global fossil fuel CO2 emissions arise from urbanized and industrialized areas. Bottom-up inventories quantify them but with large uncertainties. In 2010–2011, the first atmospheric in situ CO2 measurement network for Paris, the capital of France, began operating with the aim of monitoring the regional atmospheric impact of the emissions coming from this megacity. Five stations sampled air along a northeast–southwest axis that corresponds to the direction of the dominant winds. Two stations are classified as rural (Traînou – TRN; Montgé-en-Goële – MON, two are peri-urban (Gonesse – GON; Gif-sur-Yvette – GIF and one is urban (EIF, located on top of the Eiffel Tower. In this study, we analyze the diurnal, synoptic and seasonal variability of the in situ CO2 measurements over nearly 1 year (8 August 2010–13 July 2011. We compare these datasets with remote CO2 measurements made at Mace Head (MHD on the Atlantic coast of Ireland and support our analysis with atmospheric boundary layer height (ABLH observations made in the center of Paris and with both modeled and observed meteorological fields. The average hourly CO2 diurnal cycles observed at the regional stations are mostly driven by the CO2 biospheric cycle, the ABLH cycle and the proximity to urban CO2 emissions. Differences of several µmol mol−1 (ppm can be observed from one regional site to the other. The more the site is surrounded by urban sources (mostly residential and commercial heating, and traffic, the more the CO2 concentration is elevated, as is the associated variability which reflects the variability of the urban sources. Furthermore, two sites with inlets high above ground level (EIF and TRN show a phase shift of the CO2 diurnal cycle of a few hours compared to lower sites due to a strong coupling with the boundary layer diurnal cycle. As a consequence, the existence of a CO2 vertical gradient above Paris can be inferred, whose amplitude depends

What would dense atmospheric observation networks bring to the quantification of city CO2 emissions?

Science.gov (United States)

Wu, Lin; Broquet, Grégoire; Ciais, Philippe; Bellassen, Valentin; Vogel, Felix; Chevallier, Frédéric; Xueref-Remy, Irène; Wang, Yilong

2016-06-01

Cities currently covering only a very small portion ( directly release to the atmosphere about 44 % of global energy-related CO2, but they are associated with 71-76 % of CO2 emissions from global final energy use. Although many cities have set voluntary climate plans, their CO2 emissions are not evaluated by the monitoring, reporting, and verification (MRV) procedures that play a key role for market- or policy-based mitigation actions. Here we analyze the potential of a monitoring tool that could support the development of such procedures at the city scale. It is based on an atmospheric inversion method that exploits inventory data and continuous atmospheric CO2 concentration measurements from a network of stations within and around cities to estimate city CO2 emissions. This monitoring tool is configured for the quantification of the total and sectoral CO2 emissions in the Paris metropolitan area (˜ 12 million inhabitants and 11.4 TgC emitted in 2010) during the month of January 2011. Its performances are evaluated in terms of uncertainty reduction based on observing system simulation experiments (OSSEs). They are analyzed as a function of the number of sampling sites (measuring at 25 m a.g.l.) and as a function of the network design. The instruments presently used to measure CO2 concentrations at research stations are expensive (typically ˜ EUR 50 k per sensor), which has limited the few current pilot city networks to around 10 sites. Larger theoretical networks are studied here to assess the potential benefit of hypothetical operational lower-cost sensors. The setup of our inversion system is based on a number of diagnostics and assumptions from previous city-scale inversion experiences with real data. We find that, given our assumptions underlying the configuration of the OSSEs, with 10 stations only the uncertainty for the total city CO2 emission during 1 month is significantly reduced by the inversion by ˜ 42 %. It can be further reduced by extending the

Δ14CO2 from dark respiration in plants and its impact on the estimation of atmospheric fossil fuel CO2.

Science.gov (United States)

Xiong, Xiaohu; Zhou, Weijian; Cheng, Peng; Wu, Shugang; Niu, Zhenchuan; Du, Hua; Lu, Xuefeng; Fu, Yunchong; Burr, George S

2017-04-01

Radiocarbon ( 14 C) has been widely used for quantification of fossil fuel CO 2 (CO 2ff ) in the atmosphere and for ecosystem source partitioning studies. The strength of the technique lies in the intrinsic differences between the 14 C signature of fossil fuels and other sources. In past studies, the 14 C content of CO 2 derived from plants has been equated with the 14 C content of the atmosphere. Carbon isotopic fractionation mechanisms vary among plants however, and experimental study on fractionation associated with dark respiration is lacking. Here we present accelerator mass spectrometry (AMS) radiocarbon results of CO 2 respired from 21 plants using a lab-incubation method and associated bulk organic matter. From the respired CO 2 we determine Δ 14 C res values, and from the bulk organic matter we determine Δ 14 C bom values. A significant difference between Δ 14 C res and Δ 14 C bom (P < 0.01) was observed for all investigated plants, ranging from -42.3‰ to 10.1‰. The results show that Δ 14 C res values are in agreement with mean atmospheric Δ 14 CO 2 for several days leading up to the sampling date, but are significantly different from corresponding bulk organic Δ 14 C values. We find that although dark respiration is unlikely to significantly influence the estimation of CO 2ff , an additional bias associated with the respiration rate during a plant's growth period should be considered when using Δ 14 C in plants to quantify atmospheric CO 2ff . Copyright © 2017 Elsevier Ltd. All rights reserved.

Comparison of CO/sub 2/ measurements by two laboratories on air from bubbles in polar ice

Energy Technology Data Exchange (ETDEWEB)

Barnola, J.M.; Raynaud, D.; Neftel, A.; Oeschger, H.

1983-06-02

The CO/sub 2/ content of air enclosed in bubbles in polar ice has been reported by two laboratories (in Grenoble and Bern) to be representative of the atmospheric CO/sub 2/ concentration at the time the ice was formed. Such ice core studies indicate lower concentrations in ice formed at the end of the ice age, around 18,000 yr BP, and several explanations have been proposed for such a change. Both laboratories are currently measuring various ice cores in order to determine the pre-AD 1850 CO/sub 2/ level in the atmosphere, which relates to the partitioning of anthropogenic CO/sub 2/ among the atmospheric, biospheric and oceanic reservoirs. The two laboratories use different ice cores and different analytical procedures and, therefore, there is a need to know to what extent the measurements are quantitatively comparable. The results are presented of a comparison between the two laboratories based on measurements from the same ice core sections, which indicate that the measurements can be compared with great confidence. The results suggest that the mean CO/sub 2/ level recorded by Antartic ice for the period 800-2500 yr BP is about 260 p.p.m.v.

[Establishment and assessment of QA/QC method for sampling and analysis of atmosphere background CO2].

Science.gov (United States)

Liu, Li-xin; Zhou, Ling-xi; Xia, Ling-jun; Wang, Hong-yang; Fang, Shuang-xi

2014-12-01

To strengthen scientific management and sharing of greenhouse gas data obtained from atmospheric background stations in China, it is important to ensure the standardization of quality assurance and quality control method for background CO2 sampling and analysis. Based on the greenhouse gas sampling and observation experience of CMA, using portable sampling observation and WS-CRDS analysis technique as an example, the quality assurance measures for atmospheric CO,sampling and observation in the Waliguan station (Qinghai), the glass bottle quality assurance measures and the systematic quality control method during sample analysis, the correction method during data processing, as well as the data grading quality markers and data fitting interpolation method were systematically introduced. Finally, using this research method, the CO2 sampling and observation data at the atmospheric background stations in 3 typical regions were processed and the concentration variation characteristics were analyzed, indicating that this research method could well catch the influences of the regional and local environmental factors on the observation results, and reflect the characteristics of natural and human activities in an objective and accurate way.

13C analyses on CO2 in air using the multiflow: Application for the monitoring of atmospheric 13CO2 over hydro-electric reservoir in Quebec's Boreal region - Canada

International Nuclear Information System (INIS)

Bilodeau, G.; Hillaire-Marcel, C.; Helie, J.-F.; Fourel, F.; Varfalvy, L.

2002-01-01

The Multiflow TM preparation system is a headspace sampling device allowing extraction, purification and introduction of a gas sample into a gas-source Isotopic Ratio Mass Spectrometer for isotopic analysis. The original device was designed for 13 C measurements on CO 2 from breath tests. It has been adapted here for 13 CO 2 analysis in atmospheric low pCO 2 -samples

Using atmospheric 14CO to constrain OH variability: concept and potential for future measurements

Science.gov (United States)

Petrenko, V. V.; Murray, L. T.; Smith, A. W.

2017-12-01

The primary source of 14C-containing carbon monoxide (14CO) in the atmosphere is via 14C production from 14N by secondary cosmic rays, and the primary sink is removal by OH. Variations in the global abundance of 14CO that are not explained by variations in 14C production are mainly driven by variations in the global abundance of OH. Monitoring OH variability via methyl chloroform is becoming increasingly difficult as methyl chloroform abundance is continuing to decline. Measurements of atmospheric 14CO have previously been successfully used to infer OH variability. However, these measurements are currently only continuing at one location (Baring Head, New Zealand), which is insufficient to infer global trends. We propose to restart global 14CO monitoring with the aim of providing another constraint on OH variability. A new analytical system for 14CO sampling and measurements is in development, which will allow to strongly reduce the required sample air volumes (previously ≥ 400 L) and simplify field logistics. A set of test measurements is planned, with sampling at the Mauna Loa Observatory. Preliminary work with a state-of-the-art chemical transport model is identifying the most promising locations for global 14CO sampling.

Pleistocene atmospheric CO2 change linked to Southern Ocean nutrient utilization

Science.gov (United States)

Ziegler, M.; Diz, P.; Hall, I. R.; Zahn, R.

2011-12-01

Biological uptake of CO2 by the ocean and its subsequent storage in the abyss is intimately linked with the global carbon cycle and constitutes a significant climatic force1. The Southern Ocean is a particularly important region because its wind-driven upwelling regime brings CO2 laden abyssal waters to the surface that exchange CO2 with the atmosphere. The Subantarctic Zone (SAZ) is a CO2 sink and also drives global primary productivity as unutilized nutrients, advected with surface waters from the south, are exported via Subantarctic Mode Water (SAMW) as preformed nutrients to the low latitudes where they fuel the biological pump in upwelling areas. Recent model estimates suggest that up to 40 ppm of the total 100 ppm atmospheric pCO2 reduction during the last ice age were driven by increased nutrient utilization in the SAZ and associated feedbacks on the deep ocean alkalinity. Micro-nutrient fertilization by iron (Fe), contained in the airborne dust flux to the SAZ, is considered to be the prime factor that stimulated this elevated photosynthetic activity thus enhancing nutrient utilization. We present a millennial-scale record of the vertical stable carbon isotope gradient between subsurface and deep water (Δδ13C) in the SAZ spanning the past 350,000 years. The Δδ13C gradient, derived from planktonic and benthic foraminifera, reflects the efficiency of biological pump and is highly correlated (rxy = -0.67 with 95% confidence interval [0.63; 0.71], n=874) with the record of dust flux preserved in Antarctic ice cores6. This strongly suggests that nutrient utilization in the SAZ was dynamically coupled to dust-induced Fe fertilization across both glacial-interglacial and faster millennial timescales. In concert with ventilation changes of the deep Southern Ocean this drove ocean-atmosphere CO2 exchange and, ultimately, atmospheric pCO2 variability during the late Pleistocene.

Sintering of dioxide pellets in an oxidizing atmosphere (CO2)

International Nuclear Information System (INIS)

Santos, G.R.T.

1992-01-01

This work consists in the study of the sintering process of U O 2 pellets in an oxidizing atmosphere. Sintering tests were performed in an CO 2 atmosphere and the influence of temperature and time on the pellets density and microstructure were verified. The results obtained were compared to those from the conventional sintering process and its efficiency was confirmed. (author)

Transient Atmospheric Circulation Changes in a Grand ensemble of Idealized CO2 Increase Experiments

Science.gov (United States)

Karpechko, A.; Manzini, E.; Kornblueh, L.

2017-12-01

The yearly evolution with increasing forcing of the large-scale atmospheric circulation is examined in a 68-member ensemble of 1pctCO2 scenario experiments performed with the MPI-ESM model. Each member of the experiment ensemble is integrated for 155 years, from initial conditions taken from a 2000-yr long pre-industrial control climate experiment. The 1pctCO2 scenario experiments are conducted following the protocol of including as external forcing only a CO2 concentration increase at 1%/year, till quadrupling of CO2 concentrations. MPI-ESM is the Max-Planck-Institute Earth System Model (including coupling between the atmosphere, ocean and seaice). By averaging over the 68 members (ensemble mean), atmospheric variability is greatly reduced. Thus, it is possible to investigate the sensitivity to the climate state of the atmospheric response to CO2 doubling. Indicators of global change show the expected monotonic evolution with increasing CO2 and a weak dependence of the thermodynamical response to CO2 doubling on the climate state. The surface climate response of the atmospheric circulation, diagnosed for instance by the pressure at sea level, and the eddy-driven jet response show instead a marked dependence to the climate state, for the Northern winter season. We find that as the CO2 concentration increases above doubling, Northern winter trends in some indicators of atmospheric circulation changes decrease or even reverse, posing the question on what are the causes of this nonlinear behavior. The investigation of the role of stationary waves, the meridional overturning circulation, the decrease in Arctic sea ice and the stratospheric vortex points to the latter as a plausible cause of such nonlinear response.

Cavity ring down spectroscopy of CH, CH2, HCO, and H2CO in a premixed flat flame at both atmospheric and sub-atmospheric pressure

NARCIS (Netherlands)

Evertsen, R.; Staicu, A.D.; Oijen, van J.A.; Dam, N.J.; Goey, de L.P.H.; Meulen, ter J.J.; Cheauveau, C.; Vovelle, C.

2003-01-01

Density distributions of CH, CH2, HCO and H2CO have been measured in a premixed CH4/air flat flame by Cavity Ring Down Spectroscopy (CRDS). At atmospheric pressure problems are encountered due to the narrow spatial distribution of these species. Rotational flame Temperatures have been derived from

Recent widespread tree growth decline despite increasing atmospheric CO2.

Science.gov (United States)

Silva, Lucas C R; Anand, Madhur; Leithead, Mark D

2010-07-21

The synergetic effects of recent rising atmospheric CO(2) and temperature are expected to favor tree growth in boreal and temperate forests. However, recent dendrochronological studies have shown site-specific unprecedented growth enhancements or declines. The question of whether either of these trends is caused by changes in the atmosphere remains unanswered because dendrochronology alone has not been able to clarify the physiological basis of such trends. Here we combined standard dendrochronological methods with carbon isotopic analysis to investigate whether atmospheric changes enhanced water use efficiency (WUE) and growth of two deciduous and two coniferous tree species along a 9 degrees latitudinal gradient across temperate and boreal forests in Ontario, Canada. Our results show that although trees have had around 53% increases in WUE over the past century, growth decline (measured as a decrease in basal area increment--BAI) has been the prevalent response in recent decades irrespective of species identity and latitude. Since the 1950s, tree BAI was predominantly negatively correlated with warmer climates and/or positively correlated with precipitation, suggesting warming induced water stress. However, where growth declines were not explained by climate, WUE and BAI were linearly and positively correlated, showing that declines are not always attributable to warming induced stress and additional stressors may exist. Our results show an unexpected widespread tree growth decline in temperate and boreal forests due to warming induced stress but are also suggestive of additional stressors. Rising atmospheric CO2 levels during the past century resulted in consistent increases in water use efficiency, but this did not prevent growth decline. These findings challenge current predictions of increasing terrestrial carbon stocks under climate change scenarios.

Relationship between synoptic scale weather systems and column averaged atmospheric CO2

Science.gov (United States)

Naja, M.; Yaremchuk, A.; Onishi, R.; Maksyutov, S.; Inoue, G.

2005-12-01

Analysis of the atmospheric CO2 observations with transport models contributes to the understanding of the geographical distributions of CO2 sources and sinks. Space-borne sensors could be advantageous for CO2 measurements as they can provide wider spatial and temporal coverage. Inversion studies have suggested requirement of better than 1% precision for the space-borne observations. Since sources and sinks are inferred from spatial and temporal gradients in CO2, the space-borne observations must have no significant geographically varying biases. To study the dynamical biases in column CO2 due to possible correlation between clouds and atmospheric CO2 at synoptic scale, we have made simulations of CO2 (1988-2003) using NIES tracer transport model. Model resolution is 2.5o x 2.5o in horizontal and it has 15 vertical sigma-layers. Fluxes for (1) fossil fuels, (2) terrestrial biosphere (CASA NEP), (3) the oceans, and (4) inverse model derived monthly regional fluxes from 11 land and 11 ocean regions are used. SVD truncation is used to filter out noise in the inverse model flux time series. Model reproduces fairly well CO2 global trend and observed time series at monitoring sites around the globe. Lower column CO2 concentration is simulated inside cyclonic systems in summer over North hemispheric continental areas. Surface pressure is used as a proxy for dynamics and it is demonstrated that anomalies in column averaged CO2 has fairly good correlation with the anomalies in surface pressure. Positive correlation, as high as 0.7, has been estimated over parts of Siberia and N. America in summer time. Our explanation is based on that the low-pressure system is associated the upward motion, which leads to lower column CO2 values over these regions due to lifting of CO2-depleted summertime PBL air, and higher column CO2 over source areas. A sensitivity study without inverse model fluxes shows same correlation. The low-pressure systems' induced negative biases are 0

Regulation of senescence under elevated atmospheric CO2 via ubiquitin modification

OpenAIRE

Aoyama, Shoki; Lu, Yu; Yamaguchi, Junji; Sato, Takeo

2014-01-01

Elevated atmospheric CO2 concentration is a serious global environmental problem. Elevated CO2 affects plant growth by changing primary metabolism, closely related to carbon (C) and nitrogen (N) availability. Under sufficient N conditions, plant growth is dramatically promoted by elevated CO2. When N availability is limited, however, elevated CO2 disrupts the balance between cellular C and N (C/N). Disruption of the C/N balance is regarded as an important factor in plant growth defects. Here ...

Southern hemisphere ocean CO2 uptake: reconciling atmospheric and oceanic estimates

International Nuclear Information System (INIS)

Roy, T.; Matear, R.; Rayner, P.; Francey, R.

2003-01-01

Using an atmospheric inversion model we investigate the southern hemisphere ocean CO 2 uptake. From sensitivity studies that varied both the initial ocean flux distribution and the atmospheric data used in the inversion, our inversion predicted a total (ocean and land) uptake of 1.65-1.90 Gt C/yr. We assess the consistency between the mean southern hemisphere ocean uptake predicted by an atmospheric inversion model for the 1991-1997 period and the T99 ocean flux estimate based on observed pCO 2 in Takahashi et al. (2002; Deep-Sea Res II, 49, 1601-1622). The inversion can not match the large 1.8 Gt C/yr southern extratropical (20-90 deg S) uptake of the T99 ocean flux estimate without producing either unreasonable land fluxes in the southern mid-latitudes or by increasing the mismatches between observed and simulated atmospheric CO 2 data. The southern extratropical uptake is redistributed between the mid and high latitudes. Our results suggest that the T99 estimate of the Southern Ocean uptake south of 50 deg S is too large, and that the discrepancy reflects the inadequate representation of wintertime conditions in the T99 estimate

Precision Column CO2 Measurement from Space Using Broad Band LIDAR

Science.gov (United States)

Heaps, William S.

2009-01-01

In order to better understand the budget of carbon dioxide in the Earth's atmosphere it is necessary to develop a global high precision understanding of the carbon dioxide column. To uncover the missing sink" that is responsible for the large discrepancies in the budget as we presently understand it, calculation has indicated that measurement accuracy of 1 ppm is necessary. Because typical column average CO2 has now reached 380 ppm this represents a precision on the order of 0.25% for these column measurements. No species has ever been measured from space at such a precision. In recognition of the importance of understanding the CO2 budget to evaluate its impact on global warming the National Research Council in its decadal survey report to NASA recommended planning for a laser based total CO2 mapping mission in the near future. The extreme measurement accuracy requirements on this mission places very strong constraints on the laser system used for the measurement. This work presents an overview of the characteristics necessary in a laser system used to make this measurement. Consideration is given to the temperature dependence, pressure broadening, and pressure shift of the CO2 lines themselves and how these impact the laser system characteristics. We are examining the possibility of making precise measurements of atmospheric carbon dioxide using a broad band source of radiation. This means that many of the difficulties in wavelength control can be treated in the detector portion of the system rather than the laser source. It also greatly reduces the number of individual lasers required to make a measurement. Simplifications such as these are extremely desirable for systems designed to operate from space.

Global atmospheric carbon budget: results from an ensemble of atmospheric CO2 inversions

Directory of Open Access Journals (Sweden)

P. Peylin

2013-10-01

Full Text Available Atmospheric CO2 inversions estimate surface carbon fluxes from an optimal fit to atmospheric CO2 measurements, usually including prior constraints on the flux estimates. Eleven sets of carbon flux estimates are compared, generated by different inversions systems that vary in their inversions methods, choice of atmospheric data, transport model and prior information. The inversions were run for at least 5 yr in the period between 1990 and 2010. Mean fluxes for 2001–2004, seasonal cycles, interannual variability and trends are compared for the tropics and northern and southern extra-tropics, and separately for land and ocean. Some continental/basin-scale subdivisions are also considered where the atmospheric network is denser. Four-year mean fluxes are reasonably consistent across inversions at global/latitudinal scale, with a large total (land plus ocean carbon uptake in the north (−3.4 Pg C yr−1 (±0.5 Pg C yr−1 standard deviation, with slightly more uptake over land than over ocean, a significant although more variable source over the tropics (1.6 ± 0.9 Pg C yr−1 and a compensatory sink of similar magnitude in the south (−1.4 ± 0.5 Pg C yr−1 corresponding mainly to an ocean sink. Largest differences across inversions occur in the balance between tropical land sources and southern land sinks. Interannual variability (IAV in carbon fluxes is larger for land than ocean regions (standard deviation around 1.06 versus 0.33 Pg C yr−1 for the 1996–2007 period, with much higher consistency among the inversions for the land. While the tropical land explains most of the IAV (standard deviation ~ 0.65 Pg C yr−1, the northern and southern land also contribute (standard deviation ~ 0.39 Pg C yr−1. Most inversions tend to indicate an increase of the northern land carbon uptake from late 1990s to 2008 (around 0.1 Pg C yr−1, predominantly in North Asia. The mean seasonal cycle appears to be well constrained by the atmospheric data over

Potential of European 14CO2 observation network to estimate the fossil fuel CO2 emissions via atmospheric inversions

Science.gov (United States)

Wang, Yilong; Broquet, Grégoire; Ciais, Philippe; Chevallier, Frédéric; Vogel, Felix; Wu, Lin; Yin, Yi; Wang, Rong; Tao, Shu

2018-03-01

Combining measurements of atmospheric CO2 and its radiocarbon (14CO2) fraction and transport modeling in atmospheric inversions offers a way to derive improved estimates of CO2 emitted from fossil fuel (FFCO2). In this study, we solve for the monthly FFCO2 emission budgets at regional scale (i.e., the size of a medium-sized country in Europe) and investigate the performance of different observation networks and sampling strategies across Europe. The inversion system is built on the LMDZv4 global transport model at 3.75° × 2.5° resolution. We conduct Observing System Simulation Experiments (OSSEs) and use two types of diagnostics to assess the potential of the observation and inverse modeling frameworks. The first one relies on the theoretical computation of the uncertainty in the estimate of emissions from the inversion, known as posterior uncertainty, and on the uncertainty reduction compared to the uncertainty in the inventories of these emissions, which are used as a prior knowledge by the inversion (called prior uncertainty). The second one is based on comparisons of prior and posterior estimates of the emission to synthetic true emissions when these true emissions are used beforehand to generate the synthetic fossil fuel CO2 mixing ratio measurements that are assimilated in the inversion. With 17 stations currently measuring 14CO2 across Europe using 2-week integrated sampling, the uncertainty reduction for monthly FFCO2 emissions in a country where the network is rather dense like Germany, is larger than 30 %. With the 43 14CO2 measurement stations planned in Europe, the uncertainty reduction for monthly FFCO2 emissions is increased for the UK, France, Italy, eastern Europe and the Balkans, depending on the configuration of prior uncertainty. Further increasing the number of stations or the sampling frequency improves the uncertainty reduction (up to 40 to 70 %) in high emitting regions, but the performance of the inversion remains limited over low

Potential of European 14CO2 observation network to estimate the fossil fuel CO2 emissions via atmospheric inversions

Directory of Open Access Journals (Sweden)

Y. Wang

2018-03-01

Full Text Available Combining measurements of atmospheric CO2 and its radiocarbon (14CO2 fraction and transport modeling in atmospheric inversions offers a way to derive improved estimates of CO2 emitted from fossil fuel (FFCO2. In this study, we solve for the monthly FFCO2 emission budgets at regional scale (i.e., the size of a medium-sized country in Europe and investigate the performance of different observation networks and sampling strategies across Europe. The inversion system is built on the LMDZv4 global transport model at 3.75°  ×  2.5° resolution. We conduct Observing System Simulation Experiments (OSSEs and use two types of diagnostics to assess the potential of the observation and inverse modeling frameworks. The first one relies on the theoretical computation of the uncertainty in the estimate of emissions from the inversion, known as posterior uncertainty, and on the uncertainty reduction compared to the uncertainty in the inventories of these emissions, which are used as a prior knowledge by the inversion (called prior uncertainty. The second one is based on comparisons of prior and posterior estimates of the emission to synthetic true emissions when these true emissions are used beforehand to generate the synthetic fossil fuel CO2 mixing ratio measurements that are assimilated in the inversion. With 17 stations currently measuring 14CO2 across Europe using 2-week integrated sampling, the uncertainty reduction for monthly FFCO2 emissions in a country where the network is rather dense like Germany, is larger than 30 %. With the 43 14CO2 measurement stations planned in Europe, the uncertainty reduction for monthly FFCO2 emissions is increased for the UK, France, Italy, eastern Europe and the Balkans, depending on the configuration of prior uncertainty. Further increasing the number of stations or the sampling frequency improves the uncertainty reduction (up to 40 to 70 % in high emitting regions, but the performance of the inversion

The optimal atmospheric CO2 concentration for the growth of winter wheat (Triticum aestivum).

Science.gov (United States)

Xu, Ming

2015-07-20

This study examined the optimal atmospheric CO2 concentration of the CO2 fertilization effect on the growth of winter wheat with growth chambers where the CO2 concentration was controlled at 400, 600, 800, 1000, and 1200 ppm respectively. I found that initial increase in atmospheric CO2 concentration dramatically enhanced winter wheat growth through the CO2 fertilization effect. However, this CO2 fertilization effect was substantially compromised with further increase in CO2 concentration, demonstrating an optimal CO2 concentration of 889.6, 909.4, and 894.2 ppm for aboveground, belowground, and total biomass, respectively, and 967.8 ppm for leaf photosynthesis. Also, high CO2 concentrations exceeding the optima not only reduced leaf stomatal density, length and conductance, but also changed the spatial distribution pattern of stomata on leaves. In addition, high CO2 concentration also decreased the maximum carboxylation rate (Vc(max)) and the maximum electron transport rate (J(max)) of leaf photosynthesis. However, the high CO2 concentration had little effect on leaf length and plant height. The optimal CO2 fertilization effect found in this study can be used as an indicator in selecting and breeding new wheat strains in adapting to future high atmospheric CO2 concentrations and climate change. Copyright © 2015. Published by Elsevier GmbH.

NO emission characteristics of superfine pulverized coal combustion in the O2/CO2 atmosphere

International Nuclear Information System (INIS)

Liu, Jiaxun; Gao, Shan; Jiang, Xiumin; Shen, Jun; Zhang, Hai

2014-01-01

Highlights: • Superfine pulverized coal combustion in O 2 /CO 2 atmosphere is a new promising technology. • NO emissions of superfine pulverized coal combustion in O 2 /CO 2 mixture were focused. • Coal particle sizes have significant effects on NO emissions in O 2 /CO 2 combustion. - Abstract: The combination of O 2 /CO 2 combustion and superfine pulverized coal combustion technology can make full use of their respective merits, and solve certain inherent disadvantages of each technology. The technology of superfine pulverized coal combustion in the O 2 /CO 2 atmosphere is easy and feasible to be retrofitted with few reconstructions on the existing devices. It will become a useful and promising method in the future. In this paper, a one-dimensional drop-tube furnace system was adopted to study the NO emission characteristics of superfine pulverized coal combustion in the O 2 /CO 2 atmosphere. The effects of coal particle size, coal quality, furnace temperature, stoichiometric ratio, etc. were analyzed. It is important to note that coal particle sizes have significant influence on NO emissions in the O 2 /CO 2 combustion. For the homogeneous NO reduction, smaller coal particles can inhibit the homogeneous NO formations under fuel-rich combustion conditions, while it becomes disadvantageous for fuel-lean combustion. However, under any conditions, heterogeneous reduction is always more significant for smaller coal particle sizes, which have smoother pore surfaces and simpler pore structures. The results from this fundamental research will provide technical support for better understanding and developing this new combustion process

Declining Atmospheric pCO2 During the Late Miocene and Early Pliocene: New Insights from Paired Alkenone and Coccolith Stable Isotope Barometry

Science.gov (United States)

Phelps, S. R.; Polissar, P. J.; deMenocal, P. B.; Swann, J. P.; Guo, M. Y.; Stoll, H. M.

2015-12-01

The relationship between atmospheric CO2 concentrations and climate is broadly understood for the Cenozoic era: warmer periods are associated with higher atmospheric carbon dioxide. This understanding is supported by atmospheric samples of the past 800,000 years from ice cores, which suggest CO2 levels play a key role in regulating global climate on glacial interglacial timescales as well. In this context, the late Miocene poses a challenge: sea-surface temperatures indicate substantial global warmth, though existing data suggest atmospheric CO2 concentrations were lower than pre-industrial values. Recent work using the stable carbon and oxygen isotopic composition of coccolith calcite has demonstrated these organisms began actively diverting inorganic carbon away from calcification and to the site of photosynthesis during the late Miocene. This process occurs in culture experiments in response to low aqueous CO2 concentrations, and suggests decreasing atmospheric pCO2 values during the late Miocene. Here we present new data from ODP Site 806 in the western equatorial Pacific Ocean that supports declining atmospheric CO2 across the late Miocene. Carbon isotope values of coccolith calcite from Site 806 demonstrate carbon limitation and re-allocation of inorganic carbon to photosynthesis starting between ~8 and 6 Ma. The timing of this limitation at Site 806 precedes shifts at other ODP sites, reflecting the higher mixed layer temperature and resultant lower CO2 solubility at Site 806. New measurements of carbon isotope values from alkenones at Site 806 show an increase in photosynthetic carbon fractionation (ɛp) accompanied the carbon limitation evident from coccolith calcite stable isotope data. While higher ɛp is typically interpreted as higher CO2 concentrations, at Site 806, our data suggest it reflects enhancement of chloroplast CO2 from active carbon transport by the coccolithophore algae in response to lower CO2 concentrations. Our new data from ODP Site

A high precision mass spectrometry method for measuring O2/N2 ratios and CO2 concentrations in air

International Nuclear Information System (INIS)

Marca, A.D.; Dennis, P.F.; Etchells, A.

2002-01-01

A full, detailed understanding of the global carbon budget is needed for robust modelling of global climate and environmental change. Since the industrial revolution the carbon cycle has been shifted from a steady state in which removal of CO 2 from the atmosphere through photosynthesis is balanced by its addition through respiration. Currently increased respiration due to deforestation, modern agricultural practises and the burning of fossil fuels dominates photosynthesis resulting in modern atmospheric CO 2 concentrations some 32% higher than the year 1800 levels. However, the CO 2 concentration rises are lower than expected from known fossil fuel combustion inventories. A significant proportion of the excess CO 2 is taken up by the oceans, however a missing carbon sink must still be invoked to account for the difference between measured and expected CO 2 rises. A global greening as a result of increased photosynthesis is required to close the circle

Daily Course of CO2 Fluxes in the Atmosphere-Water System and Variable Fluorescence of Phytoplankton during the Open-Water Period for Lake Baikal according to Long-Term Measurements

Science.gov (United States)

Zavoruev, V. V.; Domysheva, V. M.; Pestunov, D. A.; Sakirko, M. V.; Panchenko, M. V.

2018-04-01

The process of gas exchange of CO2 in the atmosphere-water system and its relation to the daily course of variable fluorescence of phytoplankton is studied on the basis of long-term (2004-2014) measurements during the open water period for Lake Baikal. It is found that the decrease in photosynthetic activity of plankton is almost synchronous to the increase in the CO2 flux from atmosphere to water. It follows from comparison of the spring and summer data with December measurements that the daily decrease in variable fluorescence of phytoplankton is caused by the internal daily rhythm of the photosynthetic activity of plankton.

Experience with novel technologies for direct measurement of atmospheric NO2

Science.gov (United States)

Hueglin, Christoph; Hundt, Morten; Mueller, Michael; Schwarzenbach, Beat; Tuzson, Bela; Emmenegger, Lukas

2017-04-01

Nitrogen dioxide (NO2) is an air pollutant that has a large impact on human health and ecosystems, and it plays a key role in the formation of ozone and secondary particulate matter. Consequently, legal limit values for NO2 are set in the EU and elsewhere, and atmospheric observation networks typically include NO2 in their measurement programmes. Atmospheric NO2 is principally measured by chemiluminescence detection, an indirect measurement technique that requires conversion of NO2 into nitrogen monoxide (NO) and finally calculation of NO2 from the difference between total nitrogen oxides (NOx) and NO. Consequently, NO2 measurements with the chemiluminescence method have a relatively high measurement uncertainty and can be biased depending on the selectivity of the applied NO2 conversion method. In the past years, technologies for direct and selective measurement of NO2 have become available, e.g. cavity attenuated phase shift spectroscopy (CAPS), cavity enhanced laser absorption spectroscopy and quantum cascade laser absorption spectrometry (QCLAS). These technologies offer clear advantages over the indirect chemiluminescence method. We tested the above mentioned direct measurement techniques for NO2 over extended time periods at atmospheric measurement stations and report on our experience including comparisons with co-located chemiluminescence instruments equipped with molybdenum as well as photolytic NO2 converters. A still open issue related to the direct measurement of NO2 is instrument calibration. Accurate and traceable reference standards and NO2 calibration gases are needed. We present results from the application of different calibration strategies based on the use of static NO2 calibration gases as well as dynamic NO2 calibration gases produced by permeation and by gas-phase titration (GPT).

The Density and Compressibility of BaCO3-SrCO3-CaCO3-K2CO3-Na2CO3-Li2CO3 Liquids: New Measurements and a Systematic Trend with Cation Field Strength

Science.gov (United States)

Hurt, S. M.; Lange, R. A.; Ai, Y.

2015-12-01

The volumetric properties of multi-component carbonate liquids are required to extend thermodynamic models that describe partial melting of the deep mantle (e.g. pMELTS; Ghiorso et al., 2003) to carbonate-bearing lithologies. Carbonate in the mantle is an important reservoir of carbon, which is released to the atmosphere as CO2 through volcanism, and thus contributes to the carbon cycle. Although MgCO3 is the most important carbonate component in the mantle, it is not possible to directly measure the 1-bar density and compressibility of MgCO3 liquid because, like other alkaline-earth carbonates, it decomposes at a temperature lower than its melting temperature. Despite this challenge, Liu and Lange (2003) and O'Leary et al. (2015) showed that the one bar molar volume, thermal expansion and compressibility of the CaCO3 liquid component could be obtained by measuring the density and sound speeds of stable liquids in the CaCO3-Li2CO3-Na2CO3-K2CO3 quaternary system at one bar. In this study, this same strategy is employed on SrCO3- and BaCO3-bearing alkali carbonate liquids. The density and sound speed of seven liquids in the SrCO3-Li2CO3-Na2CO3-K2CO3 quaternary and three liquids in the BaCO3-Li2CO3-Na2CO3-K2CO3 quaternary were measured from 739-1367K, with SrCO3 and BaCO3 concentrations ranging from 10-50 mol%. The density measurements were made using the double-bob Archimedean method and sound speeds were obtained with a frequency-sweep acoustic interferometer. The molar volume and sound speed measurements were used to calculate the isothermal compressibility of each liquid, and the results show the volumetric properties mix ideally with composition. The partial molar volume and compressibility of the SrCO3 and BaCO3 components are compared to those obtained for the CaCO3 component as a function of cation field strength. The results reveal a systematic trend that allows the partial molar volume and compressibility of the MgCO3 liquid component to be estimated.

BErkeley Atmospheric CO2 Network (BEACON) - Bringing Measurements of CO2 Emissions to a School Near You

Science.gov (United States)

Teige, V. E.; Havel, E.; Patt, C.; Heber, E.; Cohen, R. C.

2011-12-01

The University of California at Berkeley in collaboration with the Chabot Space and Science Center describe a set of educational programs, workshops, and exhibits based on a multi-node greenhouse gas and air quality monitoring network being deployed over Oakland, California. Examining raw numerical data using highly engaging and effective geo-data visualization tools like Google Earth can make the science come alive for students, and provide a hook for drawing them into deeper investigations. The Climate Science Investigations teacher workshop at the Chabot Space and Science Center will make use of Google Earth, Excel, and other geo-data visualization tools to step students through the process from data acquisition to discovery. Using multiple data sources, including output from the BErkeley Atmospheric CO2 Network (BEACON) project, participants will be encouraged to explore a variety of different modes of data display toward producing a unique, and ideally insightful, illumination of the data.

Increase of atmospheric CO2 promotes phytoplankton productivity

NARCIS (Netherlands)

Schippers, P.; Lürling, M.F.L.L.W.; Scheffer, M.

2004-01-01

It is usually thought that unlike terrestrial plants, phytoplankton will not show a significant response to an increase of atmospheric CO2. Here we suggest that this view may be biased by a neglect of the effects of carbon (C) assimilation on the pH and the dissociation of the C species. We show

Advanced Intensity-Modulation Continuous-Wave Lidar Techniques for Column CO2 Measurements

Science.gov (United States)

Campbell, J. F.; Lin, B.; Obland, M. D.; Liu, Z.; Kooi, S. A.; Fan, T. F.; Nehrir, A. R.; Meadows, B.; Browell, E. V.

2016-12-01

Advanced Intensity-Modulation Continuous-Wave Lidar Techniques for Column CO2 MeasurementsJoel F. Campbell1, Bing Lin1, Michael D. Obland1, Zhaoyan Liu1, Susan Kooi2, Tai-Fang Fan2, Amin R. Nehrir1, Byron Meadows1, Edward V. Browell31NASA Langley Research Center, Hampton, VA 23681 2SSAI, NASA Langley Research Center, Hampton, VA 23681 3STARSS-II Affiliate, NASA Langley Research Center, Hampton, VA 23681 AbstractGlobal and regional atmospheric carbon dioxide (CO2) measurements for the NASA Active Sensing of CO2 Emissions over Nights, Days, and Seasons (ASCENDS) space mission and the Atmospheric Carbon and Transport (ACT) - America project are critical for improving our understanding of global CO2 sources and sinks. Advanced Intensity-Modulated Continuous-Wave (IM-CW) lidar techniques are investigated as a means of facilitating CO2 measurements from space and airborne platforms to meet the ASCENDS and ACT-America science measurement requirements. In recent numerical, laboratory and flight experiments we have successfully used the Binary Phase Shift Keying (BPSK) modulation technique to uniquely discriminate surface lidar returns from intermediate aerosol and cloud returns. We demonstrate the utility of BPSK to eliminate sidelobes in the range profile as a means of making Integrated Path Differential Absorption (IPDA) column CO2 measurements in the presence of optically thin clouds, thereby minimizing bias errors caused by the clouds. Furthermore, high accuracy and precision ranging to the surface as well as to the top of intermediate cloud layers, which is a requirement for the inversion of column CO2 number density measurements to column CO2 mixing ratios, has been demonstrated using new sub-meter hyperfine interpolation techniques that takes advantage of the periodicity of the modulation waveforms. The BPSK technique under investigation has excellent auto-correlation properties while possessing a finite bandwidth. These techniques are used in a new data processing

Developing a lower-cost atmospheric CO2 monitoring system using commercial NDIR sensor

Science.gov (United States)

Arzoumanian, E.; Bastos, A.; Gaynullin, B.; Laurent, O.; Vogel, F. R.

2017-12-01

Cities release to the atmosphere about 44 % of global energy-related CO2. It is clear that accurate estimates of the magnitude of anthropogenic and natural urban emissions are needed to assess their influence on the carbon balance. A dense ground-based CO2 monitoring network in cities would potentially allow retrieving sector specific CO2 emission estimates when combined with an atmospheric inversion framework using reasonably accurate observations (ca. 1 ppm for hourly means). One major barrier for denser observation networks can be the high cost of high precision instruments or high calibration cost of cheaper and unstable instruments. We have developed and tested a novel inexpensive NDIR sensors for CO2 measurements which fulfils cost and typical parameters requirements (i.e. signal stability, efficient handling, and connectivity) necessary for this task. Such sensors are essential in the market of emissions estimates in cities from continuous monitoring networks as well as for leak detection of MRV (monitoring, reporting, and verification) services for industrial sites. We conducted extensive laboratory tests (short and long-term repeatability, cross-sensitivities, etc.) on a series of prototypes and the final versions were also tested in a climatic chamber. On four final HPP prototypes the sensitivity to pressure and temperature were precisely quantified and correction&calibration strategies developed. Furthermore, we fully integrated these HPP sensors in a Raspberry PI platform containing the CO2 sensor and additional sensors (pressure, temperature and humidity sensors), gas supply pump and a fully automated data acquisition unit. This platform was deployed in parallel to Picarro G2401 instruments in the peri-urban site Saclay - next to Paris, and in the urban site Jussieu - Paris, France. These measurements were conducted over several months in order to characterize the long-term drift of our HPP instruments and the ability of the correction and calibration

Removing Traffic Emissions from CO2 Time Series Measured at a Tall Tower Using on-Road Measurements and WRF-Stilt Transport Modeling

Science.gov (United States)

Schmidt, A.; Rella, C.; Goeckede, M.; Hanson, C. V.; Yang, Z.; Law, B. E.

2014-12-01

In recent years, measurements of atmospheric carbon dioxide with high precision and accuracy have become increasingly important for climate change research, in particular to inform terrestrial biosphere models. Anthropogenic carbon dioxide emissions from fossil fuel burning have long been recognized to contribute a significant portion of the carbon dioxide in the atmosphere. Here, we present an approach to remove the traffic related carbon dioxide emissions from mole fractions measured at a tall tower by using the corresponding carbon monoxide measurements in combination with footprint analyses and transport modeling. This technique improves the suitability of the CO2 data to be used in inverse modeling approaches of atmosphere-biosphere exchange that do not account for non-biotic portions of CO2. In our study region in Oregon, road traffic emissions are the biggest source of anthropogenic carbon dioxide and carbon monoxide. A three-day mobile campaign covering 1700 km of roads in northwestern Oregon was performed during summer of 2012 using a laser-based Cavity Ring Down Spectrometer. The mobile measurements incorporated different roads including main highways, urban streets, and back-roads, largely within the typical footprint of a tall CO2 observation tower in Oregon's Willamette Valley. For the first time, traffic related CO:CO2 emission ratios were measured directly at the sources during an on-road campaign under a variety of different driving conditions. An average emission ratio of 7.43 (±1.80) ppb CO per ppm CO2 was obtained for the study region and applied to separate the traffic related portion of CO2 from the mole fraction time series. The road traffic related portion of the CO2 mole fractions measured at the tower site reached maximum values from 9.8 to 12 ppm, depending on the height above the surface, during summer 2012.

Broadening of spectral lines of CO2, N2O , H2CO, HCN, and H2S by pressure of gases dominant in planetary atmospheres (H2, He and CO2)

Science.gov (United States)

Samuels, Shanelle; Gordon, Iouli; Tan, Yan

2018-01-01

HITRAN1,2 is a compilation of spectroscopic parameters that a variety of computer codes use to predict and simulate the transmission and emission of light in planetary atmospheres. The goal of this project is to add to the potential of the HITRAN database towards the exploration of the planetary atmospheres by including parameters describing broadening of spectral lines by H2, CO2, and He. These spectroscopic data are very important for the study of the hydrogen and helium-rich atmospheres of gas giants as well as rocky planets with volcanic activities, including Venus and Mars, since their atmospheres are dominated by CO2. First step in this direction was accomplished by Wilzewski et al.3 where this was done for SO2, NH3, HF, HCl, OCS and C2H2. The molecules investigated in this work were CO2, N2O, H2CO, HCN and H2S. Line-broadening coefficients, line shifts and temperature-dependence exponents for transitions of these molecules perturbed by H2, CO2 and He have been assembled from available peer-reviewed experimental and theoretical sources. The data was evaluated and the database was populated with these data and their extrapolations/interpolations using semi-empirical models that were developed to this end.Acknowledgements: Financial support from NASA PDART grant NNX16AG51G and the Smithsonian Astrophysical Observatory Latino Initiative Program from the Latino Initiatives Pool, administered by the Smithsonian Latino Center is gratefully acknowledged.References: 1. HITRAN online http://hitran.org/2. Gordon, I.E., Rothman, L.S., Hill, C., Kochanov, R.V., Tan, Y., et al., 2017. The HITRAN2016 Molecular Spectroscopic Database. J. Quant. Spectrosc. Radiat. Transf. doi:10.1016/j.jqsrt.2017.06.0383. Wilzewski, J.S., Gordon, I.E., Kochanov, R. V., Hill, C., Rothman, L.S., 2016. H2, He, and CO2 line-broadening coefficients, pressure shifts and temperature-dependence exponents for the HITRAN database. Part 1: SO2, NH3, HF, HCl, OCS and C2H2. J. Quant. Spectrosc. Radiat

Atmospheric CO2 concentration effects on rice water use and biomass production.

Directory of Open Access Journals (Sweden)

Uttam Kumar

Full Text Available Numerous studies have addressed effects of rising atmospheric CO2 concentration on rice biomass production and yield but effects on crop water use are less well understood. Irrigated rice evapotranspiration (ET is composed of floodwater evaporation and canopy transpiration. Crop coefficient Kc (ET over potential ET, or ETo is crop specific according to FAO, but may decrease as CO2 concentration rises. A sunlit growth chamber experiment was conducted in the Philippines, exposing 1.44-m2 canopies of IR72 rice to four constant CO2 levels (195, 390, 780 and 1560 ppmv. Crop geometry and management emulated field conditions. In two wet (WS and two dry (DS seasons, final aboveground dry weight (agdw was measured. At 390 ppmv [CO2] (current ambient level, agdw averaged 1744 g m-2, similar to field although solar radiation was only 61% of ambient. Reduction to 195 ppmv [CO2] reduced agdw to 56±5% (SE, increase to 780 ppmv increased agdw to 128±8%, and 1560 ppmv increased agdw to 142±5%. In 2013WS, crop ET was measured by weighing the water extracted daily from the chambers by the air conditioners controlling air humidity. Chamber ETo was calculated according to FAO and empirically corrected via observed pan evaporation in chamber vs. field. For 390 ppmv [CO2], Kc was about 1 during crop establishment but increased to about 3 at flowering. 195 ppmv CO2 reduced Kc, 780 ppmv increased it, but at 1560 ppmv it declined. Whole-season crop water use was 564 mm (195 ppmv, 719 mm (390 ppmv, 928 mm (780 ppmv and 803 mm (1560 ppmv. With increasing [CO2], crop water use efficiency (WUE gradually increased from 1.59 g kg-1 (195 ppmv to 2.88 g kg-1 (1560 ppmv. Transpiration efficiency (TE measured on flag leaves responded more strongly to [CO2] than WUE. Responses of some morphological traits are also reported. In conclusion, increased CO2 promotes biomass more than water use of irrigated rice, causing increased WUE, but it does not help saving water. Comparability

Correlations among atmospheric CO[sub 2], CH[sub 4] and CO in the Arctic, March 1989

Energy Technology Data Exchange (ETDEWEB)

Conway, T.J.; Steele, L.P.; Novelli, P.C. (NOAA Climate Monitoring and Diagnostics Lab., Boulder, CO (United States))

1993-12-01

During six aircraft flights conducted as part of the third Arctic Gas and Aerosol Sampling Program (AGASP III, March 1989), 189 air samples were collected throughout the Arctic troposphere and lower stratosphere for analysis of CO[sub 2], CH[sub 4] and CO. The mixing ratios of the three gases varied significantly both horizontally and vertically. Elevated concentrations were found in layers with high anthropogenic aerosol concentrations (Arctic Haze). The mixing ratios of CO[sub 2], CH[sub 4] and CO were highly correlated on all flights. A linear regression of CH[sub 4] vs CO[sub 2] for pooled data from all flights yielded a correlation coefficient (r[sup 2]) of 0.88 and a slope of 13.5 ppb CH[sub 4]/ppm CO[sub 2] (n 186). For CO vs CO[sub 2] a pooled linear regression gave r[sup 2] 0.91 and a slope of 15.8 ppb CO/ppm CO[sub 2] (n 182). Carbon dioxide CH[sub 4] and CO also exhibited mean vertical gradients with slopes of 0.37, -4.4 and -4.2 ppb km[sup -1], respectively. Since the carbon dioxide variations observed in the Arctic atmosphere during winter are due primarily to variations in the emissions and transport of anthropogenic CO[sub 2] from Europe and Asia, the strong correlations that we have found suggest that a similar interpretation applies to CH[sub 4] and CO. Using reliable estimates of CO[sub 2] emissions for the source regions and the measured CH[sub 4]/CO[sub 2] and CO/CO[sub 2] ratios, we estimate a regional European CH[sub 4] source of 47[+-] 6 Tg CH[sub 4] yr[sup -1] that may be associated with fossil fuel combustion. A similar calculation for CO results in an estimated regional CO source of 82[+-]2 Tg CO yr[sup -1]. 31 refs., 7 figs., 4 tabs.

Effects of long-term elevated atmospheric CO2 concentrations on Pinus ponderosa

International Nuclear Information System (INIS)

Surano, K.A.; Kercher, J.R.

1993-01-01

This report details the results from an experiment of the effects of long-term elevated atmospheric CO 2 concentrations on ponderosa pine (Pinus ponderosa Laws.) saplings and seedlings. The study began in 1983 as a pilot study designed to explore the feasibility of using open-top chambers for continuous multi-year exposures on sapling-sized trees and to examine possible CO 2 responses so that future research could be adequately designed. however, following the first year of exposure, preliminary results from the study indicated that measurements of CO 2 responses should be intensified. Open-top chambers proved suitable for use in multiyear exposures of mature trees. With respect to the preliminary examination of CO 2 responses, many interesting observations were made. The nature of the preliminary results suggests that future long-term field CO 2 exposures on perennial species may be critical to the understanding and preparation for future environments. Other research reported here attempted to adapt an existing western coniferous forest growth and succession model for use in elevated CO 2 scenarios using differential species responses, and assessed the usefulness of the model in that regard. Seven papers have been processed separately for inclusion in the appropriate data bases

The future role of reforestation in reducing buildup of atmospheric CO2

International Nuclear Information System (INIS)

Marland, G.

1993-01-01

Among the options posed for mitigating the buildup of atmospheric CO 2 is planting new forest areas to sequester carbon from the atmosphere. Among the questions of interest in modeling the global carbon cycle is the extent to which reforestation is likely to succeed in providing physical removal of CO 2 from the atmosphere. There are many strategies for using forest land to mitigate the atmospheric buildup of CO 2 : decreasing the rate at which forests are cleared for other land uses, increasing the density of carbon storage in existing forests, improving the rate and efficiency at which forest products are used in the place of other energy intensive products, substitution of renewable wood fuels for fossil fuels, improved management of forests and agroforestry, and increasing the amount of land in standing forest. Because increasing the area of forests has social, political, and economic limitations; in addition to physical limitations; it is hard to envision a large increase in forest area except where there are associated economic benefits. The authors speculation is that, over the next several decades, the forest strategies most likely to be pursued for the express purpose of CO 2 mitigation are those which provide more or more-efficient substitution of forest products for energy or energy-intensive resources and that the physical accumulation of additional carbon in forests will be of lesser importance

Exchange of carbonyl sulfide (OCS) between soils and atmosphere under various CO2 concentrations

Science.gov (United States)

Bunk, Rüdiger; Behrendt, Thomas; Yi, Zhigang; Andreae, Meinrat O.; Kesselmeier, Jürgen

2017-06-01

A new continuous integrated cavity output spectroscopy analyzer and an automated soil chamber system were used to investigate the exchange processes of carbonyl sulfide (OCS) between soils and the atmosphere under laboratory conditions. The exchange patterns of OCS between soils and the atmosphere were found to be highly dependent on soil moisture and ambient CO2 concentration. With increasing soil moisture, OCS exchange ranged from emission under dry conditions to an uptake within an optimum moisture range, followed again by emission at high soil moisture. Elevated CO2 was found to have a significant impact on the exchange rate and direction as tested with several soils. There is a clear tendency toward a release of OCS at higher CO2 levels (up to 7600 ppm), which are typical for the upper few centimeters within soils. At high soil moisture, the release of OCS increased sharply. Measurements after chloroform vapor application show that there is a biotic component to the observed OCS exchange. Furthermore, soil treatment with the fungi inhibitor nystatin showed that fungi might be the dominant OCS consumers in the soils we examined. We discuss the influence of soil moisture and elevated CO2 on the OCS exchange as a change in the activity of microbial communities. Physical factors such as diffusivity that are governed by soil moisture also play a role. Comparing KM values of the enzymes to projected soil water CO2 concentrations showed that competitive inhibition is unlikely for carbonic anhydrase and PEPCO but might occur for RubisCO at higher CO2 concentrations.

Scaling laws for perturbations in the ocean–atmosphere system following large CO2 emissions

OpenAIRE

Towles, N.; Olson, P.; Gnanadesikan, A.

2015-01-01

Scaling relationships are derived for the perturbations to atmosphere and ocean variables from large transient CO2 emissions. Using the carbon cycle model LOSCAR (Zeebe et al., 2009; Zeebe, 2012b) we calculate perturbations to atmosphere temperature and total carbon, ocean temperature, total ocean carbon, pH, and alkalinity, marine sediment carbon, plus carbon-13 isotope anomalies in the ocean and atmosphere resulting from idealized CO2 emission events. The...

Isotope ratios of H, C, and O in CO2 and H2O of the martian atmosphere.

Science.gov (United States)

Webster, Chris R; Mahaffy, Paul R; Flesch, Gregory J; Niles, Paul B; Jones, John H; Leshin, Laurie A; Atreya, Sushil K; Stern, Jennifer C; Christensen, Lance E; Owen, Tobias; Franz, Heather; Pepin, Robert O; Steele, Andrew; Achilles, Cherie; Agard, Christophe; Alves Verdasca, José Alexandre; Anderson, Robert; Anderson, Ryan; Archer, Doug; Armiens-Aparicio, Carlos; Arvidson, Ray; Atlaskin, Evgeny; Aubrey, Andrew; Baker, Burt; Baker, Michael; Balic-Zunic, Tonci; Baratoux, David; Baroukh, Julien; Barraclough, Bruce; Bean, Keri; Beegle, Luther; Behar, Alberto; Bell, James; Bender, Steve; Benna, Mehdi; Bentz, Jennifer; Berger, Gilles; Berger, Jeff; Berman, Daniel; Bish, David; Blake, David F; Blanco Avalos, Juan J; Blaney, Diana; Blank, Jen; Blau, Hannah; Bleacher, Lora; Boehm, Eckart; Botta, Oliver; Böttcher, Stephan; Boucher, Thomas; Bower, Hannah; Boyd, Nick; Boynton, Bill; Breves, Elly; Bridges, John; Bridges, Nathan; Brinckerhoff, William; Brinza, David; Bristow, Thomas; Brunet, Claude; Brunner, Anna; Brunner, Will; Buch, Arnaud; Bullock, Mark; Burmeister, Sönke; Cabane, Michel; Calef, Fred; Cameron, James; Campbell, John; Cantor, Bruce; Caplinger, Michael; Caride Rodríguez, Javier; Carmosino, Marco; Carrasco Blázquez, Isaías; Charpentier, Antoine; Chipera, Steve; Choi, David; Clark, Benton; Clegg, Sam; Cleghorn, Timothy; Cloutis, Ed; Cody, George; Coll, Patrice; Conrad, Pamela; Coscia, David; Cousin, Agnès; Cremers, David; Crisp, Joy; Cros, Alain; Cucinotta, Frank; d'Uston, Claude; Davis, Scott; Day, Mackenzie; de la Torre Juarez, Manuel; DeFlores, Lauren; DeLapp, Dorothea; DeMarines, Julia; DesMarais, David; Dietrich, William; Dingler, Robert; Donny, Christophe; Downs, Bob; Drake, Darrell; Dromart, Gilles; Dupont, Audrey; Duston, Brian; Dworkin, Jason; Dyar, M Darby; Edgar, Lauren; Edgett, Kenneth; Edwards, Christopher; Edwards, Laurence; Ehlmann, Bethany; Ehresmann, Bent; Eigenbrode, Jen; Elliott, Beverley; Elliott, Harvey; Ewing, Ryan; Fabre, Cécile; Fairén, Alberto; Farley, Ken; Farmer, Jack; Fassett, Caleb; Favot, Laurent; Fay, Donald; Fedosov, Fedor; Feldman, Jason; Feldman, Sabrina; Fisk, Marty; Fitzgibbon, Mike; Floyd, Melissa; Flückiger, Lorenzo; Forni, Olivier; Fraeman, Abby; Francis, Raymond; François, Pascaline; Freissinet, Caroline; French, Katherine Louise; Frydenvang, Jens; Gaboriaud, Alain; Gailhanou, Marc; Garvin, James; Gasnault, Olivier; Geffroy, Claude; Gellert, Ralf; Genzer, Maria; Glavin, Daniel; Godber, Austin; Goesmann, Fred; Goetz, Walter; Golovin, Dmitry; Gómez Gómez, Felipe; Gómez-Elvira, Javier; Gondet, Brigitte; Gordon, Suzanne; Gorevan, Stephen; Grant, John; Griffes, Jennifer; Grinspoon, David; Grotzinger, John; Guillemot, Philippe; Guo, Jingnan; Gupta, Sanjeev; Guzewich, Scott; Haberle, Robert; Halleaux, Douglas; Hallet, Bernard; Hamilton, Vicky; Hardgrove, Craig; Harker, David; Harpold, Daniel; Harri, Ari-Matti; Harshman, Karl; Hassler, Donald; Haukka, Harri; Hayes, Alex; Herkenhoff, Ken; Herrera, Paul; Hettrich, Sebastian; Heydari, Ezat; Hipkin, Victoria; Hoehler, Tori; Hollingsworth, Jeff; Hudgins, Judy; Huntress, Wesley; Hurowitz, Joel; Hviid, Stubbe; Iagnemma, Karl; Indyk, Steve; Israël, Guy; Jackson, Ryan; Jacob, Samantha; Jakosky, Bruce; Jensen, Elsa; Jensen, Jaqueline Kløvgaard; Johnson, Jeffrey; Johnson, Micah; Johnstone, Steve; Jones, Andrea; Joseph, Jonathan; Jun, Insoo; Kah, Linda; Kahanpää, Henrik; Kahre, Melinda; Karpushkina, Natalya; Kasprzak, Wayne; Kauhanen, Janne; Keely, Leslie; Kemppinen, Osku; Keymeulen, Didier; Kim, Myung-Hee; Kinch, Kjartan; King, Penny; Kirkland, Laurel; Kocurek, Gary; Koefoed, Asmus; Köhler, Jan; Kortmann, Onno; Kozyrev, Alexander; Krezoski, Jill; Krysak, Daniel; Kuzmin, Ruslan; Lacour, Jean Luc; Lafaille, Vivian; Langevin, Yves; Lanza, Nina; Lasue, Jeremie; Le Mouélic, Stéphane; Lee, Ella Mae; Lee, Qiu-Mei; Lees, David; Lefavor, Matthew; Lemmon, Mark; Lepinette Malvitte, Alain; Léveillé, Richard; Lewin-Carpintier, Éric; Lewis, Kevin; Li, Shuai; Lipkaman, Leslie; Little, Cynthia; Litvak, Maxim; Lorigny, Eric; Lugmair, Guenter; Lundberg, Angela; Lyness, Eric; Madsen, Morten; Maki, Justin; Malakhov, Alexey; Malespin, Charles; Malin, Michael; Mangold, Nicolas; Manhes, Gérard; Manning, Heidi; Marchand, Geneviève; Marín Jiménez, Mercedes; Martín García, César; Martin, Dave; Martin, Mildred; Martínez-Frías, Jesús; Martín-Soler, Javier; Martín-Torres, F Javier; Mauchien, Patrick; Maurice, Sylvestre; McAdam, Amy; McCartney, Elaina; McConnochie, Timothy; McCullough, Emily; McEwan, Ian; McKay, Christopher; McLennan, Scott; McNair, Sean; Melikechi, Noureddine; Meslin, Pierre-Yves; Meyer, Michael; Mezzacappa, Alissa; Miller, Hayden; Miller, Kristen; Milliken, Ralph; Ming, Douglas; Minitti, Michelle; Mischna, Michael; Mitrofanov, Igor; Moersch, Jeff; Mokrousov, Maxim; Molina Jurado, Antonio; Moores, John; Mora-Sotomayor, Luis; Morookian, John Michael; Morris, Richard; Morrison, Shaunna; Mueller-Mellin, Reinhold; Muller, Jan-Peter; Muñoz Caro, Guillermo; Nachon, Marion; Navarro López, Sara; Navarro-González, Rafael; Nealson, Kenneth; Nefian, Ara; Nelson, Tony; Newcombe, Megan; Newman, Claire; Newsom, Horton; Nikiforov, Sergey; Nixon, Brian; Noe Dobrea, Eldar; Nolan, Thomas; Oehler, Dorothy; Ollila, Ann; Olson, Timothy; de Pablo Hernández, Miguel Ángel; Paillet, Alexis; Pallier, Etienne; Palucis, Marisa; Parker, Timothy; Parot, Yann; Patel, Kiran; Paton, Mark; Paulsen, Gale; Pavlov, Alex; Pavri, Betina; Peinado-González, Verónica; Peret, Laurent; Perez, Rene; Perrett, Glynis; Peterson, Joe; Pilorget, Cedric; Pinet, Patrick; Pla-García, Jorge; Plante, Ianik; Poitrasson, Franck; Polkko, Jouni; Popa, Radu; Posiolova, Liliya; Posner, Arik; Pradler, Irina; Prats, Benito; Prokhorov, Vasily; Purdy, Sharon Wilson; Raaen, Eric; Radziemski, Leon; Rafkin, Scot; Ramos, Miguel; Rampe, Elizabeth; Raulin, François; Ravine, Michael; Reitz, Günther; Rennó, Nilton; Rice, Melissa; Richardson, Mark; Robert, François; Robertson, Kevin; Rodriguez Manfredi, José Antonio; Romeral-Planelló, Julio J; Rowland, Scott; Rubin, David; Saccoccio, Muriel; Salamon, Andrew; Sandoval, Jennifer; Sanin, Anton; Sans Fuentes, Sara Alejandra; Saper, Lee; Sarrazin, Philippe; Sautter, Violaine; Savijärvi, Hannu; Schieber, Juergen; Schmidt, Mariek; Schmidt, Walter; Scholes, Daniel; Schoppers, Marcel; Schröder, Susanne; Schwenzer, Susanne; Sebastian Martinez, Eduardo; Sengstacken, Aaron; Shterts, Ruslan; Siebach, Kirsten; Siili, Tero; Simmonds, Jeff; Sirven, Jean-Baptiste; Slavney, Susie; Sletten, Ronald; Smith, Michael; Sobrón Sánchez, Pablo; Spanovich, Nicole; Spray, John; Squyres, Steven; Stack, Katie; Stalport, Fabien; Stein, Thomas; Stewart, Noel; Stipp, Susan Louise Svane; Stoiber, Kevin; Stolper, Ed; Sucharski, Bob; Sullivan, Rob; Summons, Roger; Sumner, Dawn; Sun, Vivian; Supulver, Kimberley; Sutter, Brad; Szopa, Cyril; Tan, Florence; Tate, Christopher; Teinturier, Samuel; ten Kate, Inge; Thomas, Peter; Thompson, Lucy; Tokar, Robert; Toplis, Mike; Torres Redondo, Josefina; Trainer, Melissa; Treiman, Allan; Tretyakov, Vladislav; Urqui-O'Callaghan, Roser; Van Beek, Jason; Van Beek, Tessa; VanBommel, Scott; Vaniman, David; Varenikov, Alexey; Vasavada, Ashwin; Vasconcelos, Paulo; Vicenzi, Edward; Vostrukhin, Andrey; Voytek, Mary; Wadhwa, Meenakshi; Ward, Jennifer; Weigle, Eddie; Wellington, Danika; Westall, Frances; Wiens, Roger Craig; Wilhelm, Mary Beth; Williams, Amy; Williams, Joshua; Williams, Rebecca; Williams, Richard B; Wilson, Mike; Wimmer-Schweingruber, Robert; Wolff, Mike; Wong, Mike; Wray, James; Wu, Megan; Yana, Charles; Yen, Albert; Yingst, Aileen; Zeitlin, Cary; Zimdar, Robert; Zorzano Mier, María-Paz

2013-07-19

Stable isotope ratios of H, C, and O are powerful indicators of a wide variety of planetary geophysical processes, and for Mars they reveal the record of loss of its atmosphere and subsequent interactions with its surface such as carbonate formation. We report in situ measurements of the isotopic ratios of D/H and (18)O/(16)O in water and (13)C/(12)C, (18)O/(16)O, (17)O/(16)O, and (13)C(18)O/(12)C(16)O in carbon dioxide, made in the martian atmosphere at Gale Crater from the Curiosity rover using the Sample Analysis at Mars (SAM)'s tunable laser spectrometer (TLS). Comparison between our measurements in the modern atmosphere and those of martian meteorites such as ALH 84001 implies that the martian reservoirs of CO2 and H2O were largely established ~4 billion years ago, but that atmospheric loss or surface interaction may be still ongoing.

Coastal upwelling fluxes of O2, N2O, and CO2 assessed from continuous atmospheric observations at Trinidad, California

Directory of Open Access Journals (Sweden)

T. J. Lueker

2004-01-01

Full Text Available Continuous atmospheric records of O2/N2, CO2 and N2O obtained at Trinidad, California document the effects of air-sea exchange during coastal upwelling and plankton bloom events. The atmospheric records provide continuous observations of air-sea fluxes related to synoptic scale upwelling events over several upwelling seasons. Combined with satellite, buoy and local meteorology data, calculated anomalies in O2/N2 and N2O were utilized in a simple atmospheric transport model to compute air-sea fluxes during coastal upwelling. CO2 fluxes were linked to the oceanic component of the O2 fluxes through local hydrographic data and estimated as a function of upwelling intensity (surface ocean temperature and wind speed. Regional air-sea fluxes of O2/N2, N2O, and CO2 during coastal upwelling were estimated with the aid of satellite wind and SST data. Upwelling CO2 fluxes were found to represent ~10% of export production along the northwest coast of North America. Synoptic scale upwelling events impact the net exchange of atmospheric CO2 along the coastal margin, and will vary in response to the frequency and duration of alongshore winds that are subject to climate change.

Intensity Modulation Techniques for Continuous-Wave Lidar for Column CO2 Measurements

Science.gov (United States)

Campbell, J. F.; Lin, B.; Obland, M. D.; Kooi, S. A.; Fan, T. F.; Meadows, B.; Browell, E. V.; Erxleben, W. H.; McGregor, D.; Dobler, J. T.; Pal, S.; O'Dell, C.

2017-12-01

Global and regional atmospheric carbon dioxide (CO2) measurements for the NASA Active Sensing of CO2 Emissions over Nights, Days, and Seasons (ASCENDS) space mission and the Atmospheric Carbon and Transport (ACT) - America project are critical for improving our understanding of global CO2 sources and sinks. Advanced Intensity-Modulated Continuous-Wave (IM-CW) lidar techniques are investigated as a means of facilitating CO2 measurements from space and airborne platforms to meet the ASCENDS and ACT-America science measurement requirements. In recent numerical, laboratory and flight experiments we have successfully used the Binary Phase Shift Keying (BPSK) and Linear Swept Frequency modulations to uniquely discriminate surface lidar returns from intermediate aerosol and cloud returns. We demonstrate the utility of BPSK to eliminate sidelobes in the range profile as a means of making Integrated Path Differential Absorption (IPDA) column CO2 measurements in the presence of optically thin clouds, thereby eliminating bias errors caused by the clouds. Furthermore, high accuracy and precision ranging to the surface as well as to the top of intermediate cloud layers, which is a requirement for the inversion of column CO2 number density measurements to column CO2 mixing ratios, has been demonstrated using new hyperfine interpolation techniques that take advantage of the periodicity of the modulation waveforms. This approach works well for both BPSK and linear swept-frequency modulation techniques and provides very high (at sub-meter level) range resolution. We compare BPSK to linear swept frequency and introduce a new technique to eliminate sidelobes in situations from linear swept frequency where the SNR is high with results that rival BPSK. We also investigate the effects of non-linear modulators, which can in some circumstances degrade the orthogonality of the waveforms, and show how to avoid this. These techniques are used in a new data processing architecture written in

Elevated atmospheric CO2 increases microbial growth rates and enzymes activity in soil

Science.gov (United States)

Blagodatskaya, Evgenia; Blagodatsky, Sergey; Dorodnikov, Maxim; Kuzyakov, Yakov

2010-05-01

Increasing the belowground translocation of assimilated carbon by plants grown under elevated CO2 can cause a shift in the structure and activity of the microbial community responsible for the turnover of organic matter in soil. We investigated the long-term effect of elevated CO2 in the atmosphere on microbial biomass and specific growth rates in root-free and rhizosphere soil. The experiments were conducted under two free air carbon dioxide enrichment (FACE) systems: in Hohenheim and Braunschweig, as well as in the intensively managed forest mesocosm of the Biosphere 2 Laboratory (B2L) in Oracle, AZ. Specific microbial growth rates (μ) were determined using the substrate-induced respiration response after glucose and/or yeast extract addition to the soil. We evaluated the effect of elevated CO2 on b-glucosidase, chitinase, phosphatase, and sulfatase to estimate the potential enzyme activity after soil amendment with glucose and nutrients. For B2L and both FACE systems, up to 58% higher μ were observed under elevated vs. ambient CO2, depending on site, plant species and N fertilization. The μ-values increased linearly with atmospheric CO2 concentration at all three sites. The effect of elevated CO2 on rhizosphere microorganisms was plant dependent and increased for: Brassica napus=Triticum aestivumyeast extract then for those growing on glucose, i.e. the effect of elevated CO2 was smoothed on rich vs. simple substrate. So, the r/K strategies ratio can be better revealed by studying growth on simple (glucose) than on rich substrate mixtures (yeast extract). After adding glucose, enzyme activities under elevated CO2 were 1.2-1.9-fold higher than under ambient CO2. This indicates the increased activity of microorganisms, which leads to accelerated C turnover in soil under elevated CO2. Our results clearly showed that the functional characteristics of the soil microbial community (i.e. specific growth rates and enzymes activity) rather than total microbial biomass

XPS study on the surface reaction of uranium metal in H2 and H2-CO atmospheres

International Nuclear Information System (INIS)

Wang Xiaolin; Fu Yibei; Xie Renshou

1996-04-01

The surface reactions of uranium metal in H 2 and H 2 -CO atmospheres and the effects of temperature and CO on the hydriding reaction have been studied by X-ray photoelectron spectroscopy (XPS). The reaction between commercial H 2 and uranium metal at 25 degree C leads mainly to the further oxidation of surface layer of metal due to traces of water vapour. At 200 degree C, it may lead to the hydriding reaction of uranium and the hydriding increases with increasing the exposure of H 2 . Investigation indicates CO inhibits both the hydriding reaction and oxidation on the condition of H 2 -CO atmospheres. (13 refs., 10 figs.)

Mineral nutrition and plant responses to elevated levels of atmospheric CO{sub 2}

Energy Technology Data Exchange (ETDEWEB)

Ahluwalia, A.

1996-08-01

The atmospheric concentration of CO{sub 2}, a radiatively-active ({open_quotes}green-house{close_quotes}) gas, is increasing. This increase is considered a post-industrial phenomenon attributable to increasing rates of fossil fuel combustion and changing land use practices, particularly deforestation. Climate changes resulting from such elevated atmospheric CO{sub 2} levels, in addition to the direct effects of increased CO{sub 2}, are expected to modify the productivity of forests and alter species distributions. Elevated levels of CO{sub 2} have been shown, in some cases, to lead to enhanced growth rates in plants, particularly those with C{sub 3} metabolism - indicating that plant growth is CO{sub 2}-limited in these situations. Since the major process underlying growth is CO{sub 2} assimilation via photosynthesis in leaves, plant growth represents a potential for sequestering atmospheric carbon into biomass, but this potential could be hampered by plant carbon sink size. Carbon sinks are utilization sites for assimilated carbon, enabling carbon assimilation to proceed without potential inhibition from the accumulation of assimilate (photosynthate). Plant growth provides new sinks for assimilated carbon which permits greater uptake of atmospheric carbon dioxide. However, sinks are, on the whole, reduced in size by stress events due to the adverse effects of stress on photosynthetic rates and therefore growth. This document reviews some of the literature on plant responses to increasing levels of atmospheric carbon dioxide and to inadequate nutrient supply rates, and with this background, the potential for nutrient-limited plants to respond to increasing carbon dioxide is addressed. Conclusions from the literature review are then tested experimentally by means of a case study exploring carbon-nitrogen interactions in seedlings of loblolly pine.

Investigating CO2 Reservoirs at Gale Crater and Evidence for a Dense Early Atmosphere

Science.gov (United States)

Niles, P. B.; Archer, P. D.; Heil, E.; Eigenbrode, J.; McAdam, A.; Sutter, B.; Franz, H.; Navarro-Gonzalez, R.; Ming, D.; Mahaffy, P. R.;

RISING ATMOSPHERIC CO2 AND CARBON SEQUESTRATION IN FORESTS

Science.gov (United States)

Rising CO2 concentrations in the Earth's atmosphere could alter Earth's climate system, but it is thought that higher concentrations may improve plant growth by way of the fertilization effect. Forests, an important part of the Earth's carbon cycle, are postulated to sequester a...

Atmospheric Airborne Pressure Measurements Using the Oxygen A Band for the ASCENDS Mission

Science.gov (United States)

Riris, Haris; Rodriguez, Mike; Stephen, Mark; Hasselbrack, William; Allan, Graham; Mao, Jiamping,; Kawa, Stephan R.; Weaver, Clark J.

2011-01-01

We report on airborne atmospheric pressure measurements using new fiber-based laser technology and the oxygen A-band at 765 nm. Remote measurements of atmospheric temperature and pressure are required for a number of NASA Earth science missions and specifically for the Active Sensing of CO2 Emissions Over Nights, Days, and Seasons (ASCENDS) mission. Accurate measurements of tropospheric CO2 on a global scale are very important in order to better understand its sources and sinks and to improve predictions on any future climate change. The ultimate goal of a CO2 remote sensing mission, such as ASCENDS, is to derive the CO2 concentration in the atmosphere in terms of mole fraction in unit of parts-per-million (ppmv) with regard to dry air. Therefore, both CO2 and the dry air number of molecules in the atmosphere are needed in deriving this quantity. O2 is a stable molecule and uniformly mixed in the atmosphere. Measuring the O2 absorption in the atmosphere can thus be used to infer the dry air number of molecules and then used to calculate CO2 concentration. With the knowledge of atmospheric water vapor, we can then estimate the total surface pressure needed for CO2 retrievals. Our work, funded by the ESTO IIP program, uses fiber optic technology and non-linear optics to generate 765 nm laser radiation coincident with the Oxygen A-band. Our pulsed, time gated technique uses several on- and off-line wavelengths tuned to the O2 absorption line. The choice of wavelengths allows us to measure the pressure by using two adjacent O2 absorptions in the Oxygen A-band. Our retrieval algorithm fits the O2 lineshapes and derives the pressure. Our measurements compare favorably with a local weather monitor mounted outside our laboratory and a local weather station.

222Rn and 14CO2 concentrations in the surface layer of the atmosphere

International Nuclear Information System (INIS)

Holy, K.; Chudy, M.; Sivo, A.; Richtarikova, M.; Boehm, R.; Polaskova, A.; Vojtyla, P.; Bosa, I.; Hola, O.

2002-01-01

Long-term monitoring of the Δ 14 C in the atmospheric near-ground CO 2 has been realized in Bratislava and Zlkovce, situated near the nuclear power plant Jaslovske Bohunice. Until 1993, the monthly mean Δ 14 C values showed a high variability. The annual means of Δ 14 C were about 30 per mille higher at Zlkovce than in highly industrialised Bratislava. An important change in the behaviour of the 14 C data has occurred since 1993. The records from both stations show the similar course, mainly due to the fact that there do not occur deep winter minima in Bratislava. This behaviour corresponds to the lower values of the total fossil fuel CO 2 emissions in the years after 1993 when compared to the previous years. At present, both sets of data show that the 14 C concentration is about 10% above the natural level. Since 1987 also the 222 Rn concentration in the surface layer of the atmosphere has been measured in Bratislava. These measurements provided an extensive set of the 222 Rn data characteristic for the inland environment with high level of atmospheric pollution. The seasonal and daily variations of the 222 Rn concentration were observed. The investigation of the relation between the monthly mean diurnal courses of the 222 Rn concentration and the atmospheric stability proved a high correlation between them. The 222 Rn data were used to interpret the anomalous Δ 14 C values in the surface layer of the atmosphere. (author)

The declining uptake rate of atmospheric CO2 by land and ocean sinks

International Nuclear Information System (INIS)

Raupach, M.R.; Gloor, M.; Sarmiento, J.L.; Gasser, T.

2014-01-01

Through 1959-2012, an airborne fraction (AF) of 0.44 of total anthropogenic CO 2 emissions remained in the atmosphere, with the rest being taken up by land and ocean CO 2 sinks. Understanding of this uptake is critical because it greatly alleviates the emissions reductions required for climate mitigation, and also reduces the risks and damages that adaptation has to embrace. An observable quantity that reflects sink properties more directly than the AF is the CO 2 sink rate (k S ), the combined land-ocean CO 2 sink flux per unit excess atmospheric CO 2 above pre industrial levels. Here we show from observations that k S declined over 1959-2012 by a factor of about 1/3, implying that CO 2 sinks increased more slowly than excess CO 2 . Using a carbon-climate model, we attribute the decline in k S to four mechanisms: slower-than-exponential CO 2 emissions growth (35% of the trend), volcanic eruptions (25 %), sink responses to climate change (20 %), and nonlinear responses to increasing CO 2 , mainly oceanic (20 %). The first of these mechanisms is associated purely with the trajectory of extrinsic forcing, and the last two with intrinsic, feedback responses of sink processes to changes in climate and atmospheric CO 2 . Our results suggest that the effects of these intrinsic, nonlinear responses are already detectable in the global carbon cycle. Although continuing future decreases in k S will occur under all plausible CO 2 emission scenarios, the rate of decline varies between scenarios in non intuitive ways because extrinsic and intrinsic mechanisms respond in opposite ways to changes in emissions: extrinsic mechanisms cause k S to decline more strongly with increasing mitigation, while intrinsic mechanisms cause k S to decline more strongly under high-emission, low-mitigation scenarios as the carbon-climate system is perturbed further from a near-linear regime. (authors)

Recent global CO2 flux inferred from atmospheric CO2 observations and its regional analyses

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J. M. Chen

2011-11-01

Full Text Available The net surface exchange of CO2 for the years 2002–2007 is inferred from 12 181 atmospheric CO2 concentration data with a time-dependent Bayesian synthesis inversion scheme. Monthly CO2 fluxes are optimized for 30 regions of the North America and 20 regions for the rest of the globe. Although there have been many previous multiyear inversion studies, the reliability of atmospheric inversion techniques has not yet been systematically evaluated for quantifying regional interannual variability in the carbon cycle. In this study, the global interannual variability of the CO2 flux is found to be dominated by terrestrial ecosystems, particularly by tropical land, and the variations of regional terrestrial carbon fluxes are closely related to climate variations. These interannual variations are mostly caused by abnormal meteorological conditions in a few months in the year or part of a growing season and cannot be well represented using annual means, suggesting that we should pay attention to finer temporal climate variations in ecosystem modeling. We find that, excluding fossil fuel and biomass burning emissions, terrestrial ecosystems and oceans absorb an average of 3.63 ± 0.49 and 1.94 ± 0.41 Pg C yr−1, respectively. The terrestrial uptake is mainly in northern land while the tropical and southern lands contribute 0.62 ± 0.47, and 0.67 ± 0.34 Pg C yr−1 to the sink, respectively. In North America, terrestrial ecosystems absorb 0.89 ± 0.18 Pg C yr−1 on average with a strong flux density found in the south-east of the continent.

Rising atmospheric CO{sub 2} and crops: Research methodology and direct effects

Energy Technology Data Exchange (ETDEWEB)

Rogers, H. [National Soil Dynamics Laboratory, Auburn, AL (United States); Acock, B. [Systems Research Laboratory, Beltsville, MD (United States)

1993-12-31

Carbon dioxide is the food of trees and grass. Our relentless pursuit of a better life has taken us down a traffic jammed road, past smoking factories and forests. This pursuit is forcing a rise in the atmospheric CO{sub 2} level, and no one know when and if flood stage will be reached. Some thinkers have suggested that this increase of CO{sub 2} in the atmosphere will cause warming. No matter whether this prediction is realized or not, more CO{sub 2} will directly affect plants. Data from controlled observations have usually, but not always, shown benefits. Our choices of scientific equipment for gathering CO{sub 2} response data are critical since we must see what is happening through the eye of the instrument. The signals derived from our sensors will ultimately determine the truth of our conclusions, conclusion which will profoundly influence our policy decisions. Experimental gear is selected on the basis of scale of interest and problem to be addressed. Our imaginations and our budgets interact to set bounds on our objectives and approaches. Techniques run the gamut from cellular microprobes through whole-plant controlled environment chambers to field-scale exposure systems. Trade-offs exist among the various CO{sub 2} exposure techniques, and many factors impinge on the choice of a method. All exposure chambers are derivatives of three primary types--batch, plug flow, and continuous stirred tank reactor. Systems for the generation of controlled test atmospheres of CO{sub 2} vary in two basic ways--size and degree of control. Among the newest is free-air CO{sub 2} enrichment which allows tens of square meters of cropland to be studied.

Flask sample measurements for CO2, CH4 and CO using cavity ring-down spectrometry

Science.gov (United States)

Wang, J.-L.; Jacobson, G.; Rella, C. W.; Chang, C.-Y.; Liu, I.; Liu, W.-T.; Chew, C.; Ou-Yang, C.-F.; Liao, W.-C.; Chang, C.-C.

2013-08-01

In recent years, cavity ring-down spectrometry (CRDS) has been demonstrated to be a highly sensitive, stable and fast analytical technique for real-time in situ measurements of greenhouse gases. In this study, we propose the technique (which we call flask-CRDS) of analyzing whole air flask samples for CO2, CH4 and CO using a custom gas manifold designed to connect to a CRDS analyzer. Extremely stable measurements of these gases can be achieved over a large pressure range in the flask, from 175 to 760 Torr. The wide pressure range is conducive to flask sample measurement in three ways: (1) flask samples can be collected in low-pressure environments (e.g. high-altitude locations); (2) flask samples can be first analyzed for other trace gases with the remaining low-pressure sample for CRDS analysis of CO2, CH4 and CO; and (3) flask samples can be archived and re-analyzed for validation. The repeatability of this method (1σ of 0.07 ppm for CO2, 0.4 ppb for CH4, and 0.5 ppb for CO) was assessed by analyzing five canisters filled with the same air sample to a pressure of 200 Torr. An inter-comparison of the flask-CRDS data with in-situ CRDS measurements at a high-altitude mountain baseline station revealed excellent agreement, with differences of 0.10 ± 0.09 ppm (1σ) for CO2 and 0.9 ± 1.0 ppb for CH4. This study demonstrated that the flask-CRDS method was not only simple to build and operate but could also perform highly accurate and precise measurements of atmospheric CO2, CH4 and CO in flask samples.

Assessment of model estimates of land-atmosphere CO2 exchange across northern Eurasia

Science.gov (United States)

Rawlins, M.A.; McGuire, A.D.; Kimball, J.S.; Dass, P.; Lawrence, D.; Burke, E.; Chen, X.; Delire, C.; Koven, C.; MacDougall, A.; Peng, S.; Rinke, A.; Saito, K.; Zhang, W.; Alkama, R.; Bohn, T. J.; Ciais, P.; Decharme, B.; Gouttevin, I.; Hajima, T.; Ji, D.; Krinner, G.; Lettenmaier, D.P.; Miller, P.; Moore, J.C.; Smith, B.; Sueyoshi, T.

2015-01-01

A warming climate is altering land-atmosphere exchanges of carbon, with a potential for increased vegetation productivity as well as the mobilization of permafrost soil carbon stores. Here we investigate land-atmosphere carbon dioxide (CO2) cycling through analysis of net ecosystem productivity (NEP) and its component fluxes of gross primary productivity (GPP) and ecosystem respiration (ER) and soil carbon residence time, simulated by a set of land surface models (LSMs) over a region spanning the drainage basin of Northern Eurasia. The retrospective simulations cover the period 1960–2009 at 0.5° resolution, which is a scale common among many global carbon and climate model simulations. Model performance benchmarks were drawn from comparisons against both observed CO2 fluxes derived from site-based eddy covariance measurements as well as regional-scale GPP estimates based on satellite remote-sensing data. The site-based comparisons depict a tendency for overestimates in GPP and ER for several of the models, particularly at the two sites to the south. For several models the spatial pattern in GPP explains less than half the variance in the MODIS MOD17 GPP product. Across the models NEP increases by as little as 0.01 to as much as 0.79 g C m−2 yr−2, equivalent to 3 to 340 % of the respective model means, over the analysis period. For the multimodel average the increase is 135 % of the mean from the first to last 10 years of record (1960–1969 vs. 2000–2009), with a weakening CO2 sink over the latter decades. Vegetation net primary productivity increased by 8 to 30 % from the first to last 10 years, contributing to soil carbon storage gains. The range in regional mean NEP among the group is twice the multimodel mean, indicative of the uncertainty in CO2 sink strength. The models simulate that inputs to the soil carbon pool exceeded losses, resulting in a net soil carbon gain amid a decrease in residence time. Our analysis points to improvements in model

High-precision dual-inlet IRMS measurements of the stable isotopes of CO2 and the N2O / CO2 ratio from polar ice core samples

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T. K. Bauska

2014-11-01

Full Text Available An important constraint on mechanisms of past carbon cycle variability is provided by the stable isotopic composition of carbon in atmospheric carbon dioxide (δ13C-CO2 trapped in polar ice cores, but obtaining very precise measurements has proven to be a significant analytical challenge. Here we describe a new technique to determine the δ13C of CO2 at very high precision, as well as measuring the CO2 and N2O mixing ratios. In this method, ancient air is extracted from relatively large ice samples (~400 g with a dry-extraction "ice grater" device. The liberated air is cryogenically purified to a CO2 and N2O mixture and analyzed with a microvolume-equipped dual-inlet IRMS (Thermo MAT 253. The reproducibility of the method, based on replicate analysis of ice core samples, is 0.02‰ for δ13C-CO2 and 2 ppm and 4 ppb for the CO2 and N2O mixing ratios, respectively (1σ pooled standard deviation. Our experiments show that minimizing water vapor pressure in the extraction vessel by housing the grating apparatus in a ultralow-temperature freezer (−60 °C improves the precision and decreases the experimental blank of the method to −0.07 ± 0.04‰. We describe techniques for accurate calibration of small samples and the application of a mass-spectrometric method based on source fragmentation for reconstructing the N2O history of the atmosphere. The oxygen isotopic composition of CO2 is also investigated, confirming previous observations of oxygen exchange between gaseous CO2 and solid H2O within the ice archive. These data offer a possible constraint on oxygen isotopic fractionation during H2O and CO2 exchange below the H2O bulk melting temperature.

Wine ethanol 14C as a tracer for fossil fuel CO2 emissions in Europe: Measurements and model comparison

Science.gov (United States)

Palstra, Sanne W. L.; Karstens, Ute; Streurman, Harm-Jan; Meijer, Harro A. J.

2008-11-01

14C (radiocarbon) in atmospheric CO2 is the most direct tracer for the presence of fossil-fuel-derived CO2 (CO2-ff). We demonstrate the 14C measurement of wine ethanol as a way to determine the relative regional atmospheric CO2-ff concentration compared to a background site ("regional CO2-ff excess") for specific harvest years. The carbon in wine ethanol is directly back traceable to the atmospheric CO2 that the plants assimilate. An important advantage of using wine is that the atmosphere can be monitored annually back in time. We have analyzed a total of 165 wines, mainly from harvest years 1990-1993 and 2003-2004, among which is a semicontinuous series (1973-2004) of wines from one vineyard in southwest Germany. The results show clear spatial and temporal variations in the regional CO2-ff excess values. We have compared our measured regional CO2-ff excess values of 2003 and 2004 with those simulated by the REgional MOdel (REMO). The model results show a bias of almost +3 parts per million (ppm) CO2-ff compared with those of the observations. The modeled differences between 2003 and 2004, however, which can be used as a measure for the variability in atmospheric mixing and transport processes, show good agreement with those of the observations all over Europe. Correcting for interannual variations using modeled data produces a regional CO2-ff excess signal that is potentially useful for the verification of trends in regional fossil fuel consumption. In this fashion, analyzing 14C from wine ethanol offers the possibility to observe fossil fuel emissions back in time on many places in Europe and elsewhere.

ROOT-GROWTH AND FUNCTIONING UNDER ATMOSPHERIC CO2 ENRICHMENT

NARCIS (Netherlands)

STULEN, [No Value; DENHERTOG, J

This paper examines the extent to which atmospheric CO2 enrichment may influence growth of plant roots and function in terms of uptake of water and nutrients, and carbon allocation towards symbionts. It is concluded that changes in dry matter allocation greatly depend on the experimental conditions

Pulsed Lidar Measurements of Atmospheric CO2 Column Absorption and Range During the ASCENDS 2009-2011 Airborne Campaigns

Science.gov (United States)

Abshire, J. B.; Weaver, C. J.; Riris, H.; Mao, J.; Sun, X.; Allan, G. R.; Hasselbrack, W. E.; Browell, E. V.

2012-01-01

We have developed a pulsed lidar technique for measuring the tropospheric CO2 concentrations as a candidate for NASA's ASCENDS mission and have demonstrated the CO2 and O2 measurements from aircraft. Our technique uses two pulsed lasers allowing simultaneous measurement of a single CO2 absorption line near 1572 nm, O2 extinction in the Oxygen A-band, surface height and backscatter profile. The lasers are stepped in wavelength across the CO2 line and an O2 line doublet during the measurement. The column densities for the CO2 and O2 are estimated from the differential optical depths (DOD) of the scanned absorption lines via the IPDA technique. For the 2009 ASCENDS campaign we flew the CO2 lidar only on a Lear-25 aircraft, and measured the absorption line shapes of the CO2 line using 20 wavelength samples per scan. Measurements were made at stepped altitudes from 3 to 12.6 km over the Lamont OK, central Illinois, North Carolina, and over the Virginia Eastern Shore. Although the received signal energies were weaker than expected for ASCENDS, clear C02 line shapes were observed at all altitudes. Most flights had 5-6 altitude steps with 200-300 seconds of recorded measurements per step. We averaged every 10 seconds of measurements and used a cross-correlation approach to estimate the range to the scattering surface and the echo pulse energy at each wavelength. We then solved for the best-fit CO2 absorption line shape, and calculated the DOD of the fitted CO2 line, and computed its statistics at the various altitude steps. We compared them to CO2 optical depths calculated from spectroscopy based on HITRAN 2008 and the column number densities calculated from the airborne in-situ readings. The 2009 measurements have been analyzed in detail and they were similar on all flights. The results show clear CO2 line shape and absorption signals, which follow the expected changes with aircraft altitude from 3 to 13 km. They showed the expected nearly the linear dependence of DOD vs

Toward an estimation of daily european CO2 fluxes at high spatial resolution by inversion of atmospheric transport

International Nuclear Information System (INIS)

Carouge, C.

2006-04-01

Since the end of the 1980's, measurements of atmospheric carbon dioxide have been used to estimate global and regional fluxes of CO 2 . This is possible because CO 2 concentration variation is directly linked to flux variation by atmospheric transport. We can find the spatial and temporal distribution of fluxes from concentration measurements by 'inverting' the atmospheric transport. Until recently, most CO 2 inversions have used monthly mean CO 2 atmospheric concentration measurements to infer monthly fluxes. Considering the sparseness of the global CO 2 measurement network, fluxes were a priori aggregated on sub-continental regions and distributed on a fixed spatial pattern within these regions. Only one flux coefficient per month for each region was optimized. With this strong constraint, estimated fluxes can be biased by non-perfect distribution of fluxes within each region (aggregation error). Therefore, flux estimation at model resolution is being developed where the hard constraint of a fixed distribution within a region is replaced by a soft constraint of covariances between flux uncertainties. The use of continuous observations from an increasing number of measurement sites offers a new challenge for inverse modelers. We investigate the use of daily averaged observations to infer daily CO 2 fluxes at model resolution over Europe. We have developed a global synthesis Bayesian inversion to invert daily fluxes at model resolution (50 x 50 km over Europe) from daily averaged CO 2 concentrations. We have obtained estimated fluxes for the year 2001 over Europe using the 10 European continuous sites from the AEROCARB network. The global atmospheric model LMDZt is used with a nested grid over Europe. It is necessary to add a priori spatial and temporal correlations between flux errors to constrain the Bayesian inversion. We present the impact on estimated fluxes of three different spatial correlations based on distance between pixels, climate and vegetation

Observation of atmospheric CO2 and CO at Shangri-La station: results from the only regional station located at southwestern China

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Shuangxi Fang

2016-02-01

Full Text Available Mole fractions of atmospheric carbon dioxide (CO2 and carbon monoxide (CO have been continuously measured since September 2010 at the Shangri-La station (28.02 ° N, 99.73 ° E, 3580 masl in China using a cavity ring-down spectrometer. The station is located in the remote southwest of China, and it is the only station in that region with background conditions for greenhouse gas observations. The vegetation canopy around the station is dominated by coniferous forests and mountain meadows and there is no large city (population >1 million within a 360 km radius. Characteristics of the mole fractions, growth rates, influence of long-distance transport as well as the Weighted Potential CO Sources Contribution Function (WPSCF were studied considering data from September 2010 to May 2014. The diurnal CO2 variation in summer indicates a strong influence of regional terrestrial ecosystem with the maximum CO2 value at 7:00 (local time and the minimum in late afternoon. The highest peak-to-bottom amplitude in the diurnal cycles is in summer, with a value of 18.2±2.0 ppm. The annual growth rate of regional CO2 is estimated to be 2.5±1.0 ppm yr−1 (1-σ, which is close to that of the Mt. Waliguan World Meteorological Organization/Global Atmosphere Watch (WMO/GAW global station (2.2±0.8 ppm yr−1, that is also located at the Tibetan plateau but 900 km north. The CO mole fractions observed at Shangri-La are representative for both in large spatial scale (probably continental/subcontinental and regional scale. The annual CO growth rate is estimated to be -2.6±0.2 ppb yr−1 (1-σ. But the CO rate of decrease in continental/subcontinental scale is apparently larger than the regional scale. From the back trajectory study, it could be seen that the atmospheric CO mole fractions at Shangri-La are subjected to transport from the Northern Africa and Southwestern Asia sectors except for summer and part of autumn. The WPSCF analysis indicates that the western and

Abrupt rise in atmospheric CO2 at the onset of the Bølling/Allerød: in-situ ice core data versus true atmospheric signals

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J. Chappellaz

2011-05-01

Full Text Available During the last glacial/interglacial transition the Earth's climate underwent abrupt changes around 14.6 kyr ago. Temperature proxies from ice cores revealed the onset of the Bølling/Allerød (B/A warm period in the north and the start of the Antarctic Cold Reversal in the south. Furthermore, the B/A was accompanied by a rapid sea level rise of about 20 m during meltwater pulse (MWP 1A, whose exact timing is a matter of current debate. In-situ measured CO2 in the EPICA Dome C (EDC ice core also revealed a remarkable jump of 10 ± 1 ppmv in 230 yr at the same time. Allowing for the modelled age distribution of CO2 in firn, we show that atmospheric CO2 could have jumped by 20–35 ppmv in less than 200 yr, which is a factor of 2–3.5 greater than the CO2 signal recorded in-situ in EDC. This rate of change in atmospheric CO2 corresponds to 29–50% of the anthropogenic signal during the last 50 yr and is connected with a radiative forcing of 0.59–0.75 W m−2. Using a model-based airborne fraction of 0.17 of atmospheric CO2, we infer that 125 Pg of carbon need to be released into the atmosphere to produce such a peak. If the abrupt rise in CO2 at the onset of the B/A is unique with respect to other Dansgaard/Oeschger (D/O events of the last 60 kyr (which seems plausible if not unequivocal based on current observations, then the mechanism responsible for it may also have been unique. Available δ13CO2 data are neutral, whether the source of the carbon is of marine or terrestrial origin. We therefore hypothesise that most of the carbon might have been activated as a consequence of continental shelf flooding during MWP-1A. This potential impact of rapid sea level rise on atmospheric CO2 might define the point of no return during the last deglaciation.

Characteristics of coupled atmosphere-ocean CO2 sensitivity experiments with different ocean formulations

International Nuclear Information System (INIS)

Washington, W.M.; Meehl, G.A.

1990-01-01

The Community Climate Model at the National Center for Atmospheric Research has been coupled to a simple mixed-layer ocean model and to a coarse-grid ocean general circulation model (OGCM). This paper compares the responses of simulated climate to increases of atmospheric carbon dioxide (CO 2 ) in these two coupled models. Three types of simulations were run: (1) control runs with both ocean models, with CO 2 held constant at present-day concentrations, (2) instantaneous doubling of atmospheric CO 2 (from 330 to 660 ppm) with both ocean models, and (3) a gradually increasing (transient) CO 2 concentration starting at 330 ppm and increasing linearly at 1% per year, with the OGCM. The mixed-layer and OGCM cases exhibit increases of 3.5 C and 1.6 C, respectively, in globally averaged surface air temperature for the instantaneous doubling cases. The transient-forcing case warms 0.7 C by the end of 30 years. The mixed-layer ocean yields warmer-than-observed tropical temperatures and colder-than-observed temperatures in the higher latitudes. The coarse-grid OGCM simulates lower-than-observed sea surface temperatures (SSTs) in the tropics and higher-than-observed SSTs and reduced sea-ice extent at higher latitudes. Sensitivity in the OGCM after 30 years is much lower than in simulations with the same atmosphere coupled to a 50-m slab-ocean mixed layer. The OGCM simulates a weaker thermohaline circulation with doubled CO 2 as the high-latitude ocean-surface layer warms and freshens and the westerly wind stress decreases. Convective overturning in the OGCM decreases substantially with CO 2 warming

Characteristics of coupled atmosphere-ocean CO2 sensitivity experiments with different ocean formulations

International Nuclear Information System (INIS)

Washington, W.M.; Meehl, G.A.

1991-01-01

The Community Climate Model at the National Center for Atmospheric Research has been coupled to a simple mixed-layer ocean model and to a coarse-grid ocean general circulation model (OGCM). This paper compares the responses of simulated climate to increases of atmospheric carbon dioxide (CO 2 ) in these two coupled models. Three types of simulations were run: (1) control runs with both ocean models, with CO 2 held constant at present-day concentrations, (2) instantaneous doubling of atmospheric CO 2 (from 330 to 660 ppm) with both ocean models, and (3) a gradually increasing (transient) CO 2 concentration starting at 330 ppm and increasing linearly at 1% per year, with the OGCM. The mixed-layer and OGCM cases exhibit increases of 3.5 C and 1.6 C, respectively, in globally averaged surface air temperature for the instantaneous doubling cases. The transient-forcing case warms 0.7 C by the end of 30 years. The mixed-layer ocean yields warmer-than-observed tropical temperatures and colder-than-observed temperatures in the higher latitudes. The coarse-grid OGCM simulates lower-than-observed sea surface temperatures (SSTs) in the tropics and higher-than-observed SSTs and reduced sea-ice extent at higher latitudes. Sensitivity in the OGCM after 30 years is much lower than in simulations with the same atmosphere coupled to a 50-m slab-ocean mixed layer. The OGCM simulates a weaker thermohaline circulation with doubled CO 2 as the high-latitude ocean-surface layer warms and freshens and the westerly wind stress decreases. Convective overturning in the OGCM decreases substantially with CO 2 warming. 46 refs.; 20 figs.; 1 tab

Silicon microring refractometric sensor for atmospheric CO(2) gas monitoring.

Science.gov (United States)

Mi, Guangcan; Horvath, Cameron; Aktary, Mirwais; Van, Vien

2016-01-25

We report a silicon photonic refractometric CO(2) gas sensor operating at room temperature and capable of detecting CO(2) gas at atmospheric concentrations. The sensor uses a novel functional material layer based on a guanidine polymer derivative, which is shown to exhibit reversible refractive index change upon absorption and release of CO(2) gas molecules, and does not require the presence of humidity to operate. By functionalizing a silicon microring resonator with a thin layer of the polymer, we could detect CO(2) gas concentrations in the 0-500ppm range with a sensitivity of 6 × 10(-9) RIU/ppm and a detection limit of 20ppm. The microring transducer provides a potential integrated solution in the development of low-cost and compact CO(2) sensors that can be deployed as part of a sensor network for accurate environmental monitoring of greenhouse gases.

Analysis of the potential of near-ground measurements of CO2 and CH4 in London, UK, for the monitoring of city-scale emissions using an atmospheric transport model

Science.gov (United States)

Boon, Alex; Broquet, Grégoire; Clifford, Deborah J.; Chevallier, Frédéric; Butterfield, David M.; Pison, Isabelle; Ramonet, Michel; Paris, Jean-Daniel; Ciais, Philippe

2016-06-01

Carbon dioxide (CO2) and methane (CH4) mole fractions were measured at four near-ground sites located in and around London during the summer of 2012 with a view to investigating the potential of assimilating such measurements in an atmospheric inversion system for the monitoring of the CO2 and CH4 emissions in the London area. These data were analysed and compared with simulations using a modelling framework suited to building an inversion system: a 2 km horizontal resolution south of England configuration of the transport model CHIMERE driven by European Centre for Medium-Range Weather Forecasts (ECMWF) meteorological forcing, coupled to a 1 km horizontal resolution emission inventory (the UK National Atmospheric Emission Inventory). First comparisons reveal that local sources, which cannot be represented in the model at a 2 km resolution, have a large impact on measurements. We evaluate methods to filter out the impact of some of the other critical sources of discrepancies between the measurements and the model simulation except that of the errors in the emission inventory, which we attempt to isolate. Such a separation of the impact of errors in the emission inventory should make it easier to identify the corrections that should be applied to the inventory. Analysis is supported by observations from meteorological sites around the city and a 3-week period of atmospheric mixing layer height estimations from lidar measurements. The difficulties of modelling the mixing layer depth and thus CO2 and CH4 concentrations during the night, morning and late afternoon lead to focusing on the afternoon period for all further analyses. The discrepancies between observations and model simulations are high for both CO2 and CH4 (i.e. their root mean square (RMS) is between 8 and 12 parts per million (ppm) for CO2 and between 30 and 55 parts per billion (ppb) for CH4 at a given site). By analysing the gradients between the urban sites and a suburban or rural reference site, we

CO2 dispersion modelling over Paris region within the CO2-MEGAPARIS project

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C. Lac

2013-05-01

Full Text Available Accurate simulation of the spatial and temporal variability of tracer mixing ratios over urban areas is a challenging and interesting task needed to be performed in order to utilise CO2 measurements in an atmospheric inverse framework and to better estimate regional CO2 fluxes. This study investigates the ability of a high-resolution model to simulate meteorological and CO2 fields around Paris agglomeration during the March field campaign of the CO2-MEGAPARIS project. The mesoscale atmospheric model Meso-NH, running at 2 km horizontal resolution, is coupled with the Town Energy Balance (TEB urban canopy scheme and with the Interactions between Soil, Biosphere and Atmosphere CO2-reactive (ISBA-A-gs surface scheme, allowing a full interaction of CO2 modelling between the surface and the atmosphere. Statistical scores show a good representation of the urban heat island (UHI with stronger urban–rural contrasts on temperature at night than during the day by up to 7 °C. Boundary layer heights (BLH have been evaluated on urban, suburban and rural sites during the campaign, and also on a suburban site over 1 yr. The diurnal cycles of the BLH are well captured, especially the onset time of the BLH increase and its growth rate in the morning, which are essential for tall tower CO2 observatories. The main discrepancy is a small negative bias over urban and suburban sites during nighttime (respectively 45 m and 5 m, leading to a few overestimations of nocturnal CO2 mixing ratios at suburban sites and a bias of +5 ppm. The diurnal CO2 cycle is generally well captured for all the sites. At the Eiffel tower, the observed spikes of CO2 maxima occur every morning exactly at the time at which the atmospheric boundary layer (ABL growth reaches the measurement height. At suburban ground stations, CO2 measurements exhibit maxima at the beginning and at the end of each night, when the ABL is fully contracted, with a strong spatio-temporal variability. A

Abundances of isotopologues and calibration of CO2 greenhouse gas measurements

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P. P. Tans

2017-07-01

Full Text Available We have developed a method to calculate the fractional distribution of CO2 across all of its component isotopologues based on measured δ13C and δ18O values. The fractional distribution can be used with known total CO2 to calculate the amount of substance fraction (mole fraction of each component isotopologue in air individually. The technique is applicable to any molecule where isotopologue-specific values are desired. We used it with a new CO2 calibration system to account for isotopic differences among the primary CO2 standards that define the WMO X2007 CO2-in-air calibration scale and between the primary standards and standards in subsequent levels of the calibration hierarchy. The new calibration system uses multiple laser spectroscopic techniques to measure mole fractions of the three major CO2 isotopologues (16O12C16O, 16O13C16O, and 16O12C18O individually. The three measured values are then combined into total CO2 (accounting for the rare unmeasured isotopologues, δ13C, and δ18O values. The new calibration system significantly improves our ability to transfer the WMO CO2 calibration scale with low uncertainty through our role as the World Meteorological Organization Global Atmosphere Watch Central Calibration Laboratory for CO2. Our current estimates for reproducibility of the new calibration system are ±0.01 µmol mol−1 CO2, ±0.2 ‰ δ13C, and ±0.2 ‰ δ18O, all at 68 % confidence interval (CI.

Phenol-Formaldehyde Resin-Based Carbons for CO2 Separation at Sub-Atmospheric Pressures

Directory of Open Access Journals (Sweden)

Noelia Álvarez-Gutiérrez

2016-03-01

Full Text Available The challenge of developing effective separation and purification technologies that leave much smaller energy footprints is greater for carbon dioxide (CO2 than for other gases. In addition to its involvement in climate change, CO2 is present as an impurity in biogas and bio-hydrogen (biological production by dark fermentation, in post-combustion processes (flue gas, CO2-N2 and many other gas streams. Selected phenol-formaldehyde resin-based activated carbons prepared in our laboratory have been evaluated under static conditions (adsorption isotherms as potential adsorbents for CO2 separation at sub-atmospheric pressures, i.e., in post-combustion processes or from biogas and bio-hydrogen streams. CO2, H2, N2, and CH4 adsorption isotherms at 25 °C and up to 100 kPa were obtained using a volumetric equipment and were correlated by applying the Sips model. Adsorption equilibrium was then predicted for multicomponent gas mixtures by extending the multicomponent Sips model and the Ideal Adsorbed Solution Theory (IAST in conjunction with the Sips model. The CO2 uptakes of the resin-derived carbons from CO2-CH4, CO2-H2, and CO2-N2 at atmospheric pressure were greater than those of the reference commercial carbon (Calgon BPL. The performance of the resin-derived carbons in terms of equilibrium of adsorption seems therefore relevant to CO2 separation in post-combustion (flue gas, CO2-N2 and in hydrogen fermentation (CO2-H2, CO2-CH4.

Airborne remote-sensing of atmospheric CH4 and CO2 with MAMap: first results of measurements over wetlands in Germany and a N-S transect from Canada to Chile

Science.gov (United States)

Tretner, A.; Gerilowski, K.; Bovensmann, H.; Buchwitz, M.; Bertagnolio, P. P.; Erzinger, J.; Burrows, J.

2008-12-01

The Methane Airborne Mapper (MAMap) was designed for CO2 and CH4 remote sensing of the atmospheric column between an aircraft and the Earth's surface. The instrument is specified to detect mixing ratio variations below the aircraft of wetlands have been conducted in Germany and correlated to ground-based measurements. A first version of the data retrieval has been developed using a modified version of the WFM-DOAS algorithm. WFM-DOAS is also used for the retrieval of CH4 and CO2 column concentrations from nadir measurements by SCIAMACHY onboard ENVISAT. In November 2008, a transect from Oshawa, Canada to Punta Arenas, Chile will be flown onboard the AWI POLAR 5 aircraft. Along the flight path CH4 and CO2 measurements will be conducted by MAMap. Besides the N-S track (Canada-USA-Bahamas-Panama-Ecuador-Peru-Chile), an additional W-E track from Guayaquil (Ecuador) to Iquitos (Peru) and back is planned, covering large areas of Peruvian rainforest. One focus of this project is the evaluation of tropical rain forest and savannah as sources/sinks of CH4 and CO2. Discrepancies between the models and satellite data regarding atmospheric CH4 concentrations over the tropics have been reported in the past. A first assessment of MAMap measurements performed in 2008 over wetlands in Germany and the AWI-POLAR 5 campaign will be presented.

The declining uptake rate of atmospheric CO2 by land and ocean sinks

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M. R. Raupach

2014-07-01

Full Text Available Through 1959–2012, an airborne fraction (AF of 0.44 of total anthropogenic CO2 emissions remained in the atmosphere, with the rest being taken up by land and ocean CO2 sinks. Understanding of this uptake is critical because it greatly alleviates the emissions reductions required for climate mitigation, and also reduces the risks and damages that adaptation has to embrace. An observable quantity that reflects sink properties more directly than the AF is the CO2 sink rate (kS, the combined land–ocean CO2 sink flux per unit excess atmospheric CO2 above preindustrial levels. Here we show from observations that kS declined over 1959–2012 by a factor of about 1 / 3, implying that CO2 sinks increased more slowly than excess CO2. Using a carbon–climate model, we attribute the decline in kS to four mechanisms: slower-than-exponential CO2 emissions growth (~ 35% of the trend, volcanic eruptions (~ 25%, sink responses to climate change (~ 20%, and nonlinear responses to increasing CO2, mainly oceanic (~ 20%. The first of these mechanisms is associated purely with the trajectory of extrinsic forcing, and the last two with intrinsic, feedback responses of sink processes to changes in climate and atmospheric CO2. Our results suggest that the effects of these intrinsic, nonlinear responses are already detectable in the global carbon cycle. Although continuing future decreases in kS will occur under all plausible CO2 emission scenarios, the rate of decline varies between scenarios in non-intuitive ways because extrinsic and intrinsic mechanisms respond in opposite ways to changes in emissions: extrinsic mechanisms cause kS to decline more strongly with increasing mitigation, while intrinsic mechanisms cause kS to decline more strongly under high-emission, low-mitigation scenarios as the carbon–climate system is perturbed further from a near-linear regime.

Effects of elevated atmospheric CO2, prolonged summer drought and temperature increase on N2O and CH4 fluxes in a temperate heathland

DEFF Research Database (Denmark)

Carter, Mette Sustmann; Ambus, Per; Albert, Kristian Rost

2011-01-01

In temperate regions, climate change is predicted to increase annual mean temperature and intensify the duration and frequency of summer droughts, which together with elevated atmospheric carbon dioxide (CO2) concentrations, may affect the exchange of nitrous oxide (N2O) and methane (CH4) between...... terrestrial ecosystems and the atmosphere. We report results from the CLIMAITE experiment, where the effects of these three climate change parameters were investigated solely and in all combinations in a temperate heathland. Field measurements of N2O and CH4 fluxes took place 1–2 years after the climate...... change manipulations were initiated. The soil was generally a net sink for atmospheric CH4. Elevated temperature (T) increased the CH4 uptake by on average 10 μg C m−2 h−1, corresponding to a rise in the uptake rate of about 20%. However, during winter elevated CO2 (CO2) reduced the CH4 uptake, which...

Effects of long-term elevated atmospheric CO{sub 2} concentrations on Pinus ponderosa

Energy Technology Data Exchange (ETDEWEB)

Surano, K.A.; Kercher, J.R. [eds.

1993-10-01

This report details the results from an experiment of the effects of long-term elevated atmospheric CO{sub 2} concentrations on ponderosa pine (Pinus ponderosa Laws.) saplings and seedlings. The study began in 1983 as a pilot study designed to explore the feasibility of using open-top chambers for continuous multi-year exposures on sapling-sized trees and to examine possible CO{sub 2} responses so that future research could be adequately designed. however, following the first year of exposure, preliminary results from the study indicated that measurements of CO{sub 2} responses should be intensified. Open-top chambers proved suitable for use in multiyear exposures of mature trees. With respect to the preliminary examination of CO{sub 2} responses, many interesting observations were made. The nature of the preliminary results suggests that future long-term field CO{sub 2} exposures on perennial species may be critical to the understanding and preparation for future environments. Other research reported here attempted to adapt an existing western coniferous forest growth and succession model for use in elevated CO{sub 2} scenarios using differential species responses, and assessed the usefulness of the model in that regard. Seven papers have been processed separately for inclusion in the appropriate data bases.

Interannual variability in the atmospheric CO2 rectification over a boreal forest region

Science.gov (United States)

Chen, Baozhang; Chen, Jing M.; Worthy, Douglas E. J.

2005-08-01

Ecosystem CO2 exchange with the atmosphere and the planetary boundary layer (PBL) dynamics are correlated diurnally and seasonally. The strength of this kind of covariation is quantified as the rectifier effect, and it affects the vertical gradient of CO2 and thus the global CO2 distribution pattern. An 11-year (1990-1996, 1999-2002), continuous CO2 record from Fraserdale, Ontario (49°52'29.9″N, 81°34'12.3″W), along with a coupled vertical diffusion scheme (VDS) and ecosystem model named Boreal Ecosystem Productivity Simulator (BEPS), are used to investigate the interannual variability of the rectifier effect over a boreal forest region. The coupled model performed well (r2 = 0.70 and 0.87, at 40 m at hourly and daily time steps, respectively) in simulating CO2 vertical diffusion processes. The simulated annual atmospheric rectifier effect varies from 3.99 to 5.52 ppm, while the diurnal rectifying effect accounted for about a quarter of the annual total (22.8˜28.9%).The atmospheric rectification of CO2 is not simply influenced by terrestrial source and sink strengths, but by seasonal and diurnal variations in the land CO2 flux and their interaction with PBL dynamics. Air temperature and moisture are found to be the dominant climatic factors controlling the rectifier effect. The annual rectifier effect is highly correlated with annual mean temperature (r2 = 0.84), while annual mean air relative humidity can explain 51% of the interannual variation in rectification. Seasonal rectifier effect is also found to be more sensitive to climate variability than diurnal rectifier effect.

2-Micron Laser Transmitter for Coherent CO2 DIAL Measurement

Science.gov (United States)

Singh, Upendra N.; Bai, Yingxin; Yu, Jirong

2009-01-01

Carbon dioxide (CO2) has been recognized as one of the most important greenhouse gases. It is essential for the study of global warming to accurately measure the CO2 concentration in the atmosphere and continuously record its variation. A high repetition rate, highly efficient, Q-switched 2-micron laser system as the transmitter of a coherent differential absorption lidar for CO2 measurement has been developed in NASA Langley Research Center. This laser system is capable of making a vertical profiling of CO2 from ground and column measurement of CO2 from air and space-borne platform. The transmitter is a master-slave laser system. The master laser operates in a single frequency, either on-line or off-line of a selected CO2 absorption line. The slave laser is a Q-switched ring-cavity Ho:YLF laser which is pumped by a Tm:fiber laser. The repetition rate can be adjusted from a few hundred Hz to 10 kHz. The injection seeding success rate is from 99.4% to 99.95%. For 1 kHz operation, the output pulse energy is 5.5mJ with the pulse length of 50 ns. The optical-to-optical efficiency is 39% when the pump power is 14.5W. A Ho:YLF laser operating in the range of 2.05 micrometers can be tuned over several characteristic lines of CO2 absorption. Experimentally, a diode pumped Ho:Tm:YLF laser has been successfully used as the transmitter of coherent differential absorption lidar for the measurement of CO2 with a repetition rate of 5 Hz and pulse energy of 75 mJ. For coherent detection, high repetition rate is required for speckle averaging to obtain highly precise measurements. However, a diode pumped Ho:Tm:YLF laser can not operate in high repetition rate due to the large heat loading and up-conversion. A Tm:fiber laser pumped Ho:YLF laser with low heat loading can operate in high repetition rate. A theoretical model has been established to simulate the performance of Tm:fiber laser pumped Ho:YLF lasers. For continuous wave (CW) operation, high pump intensity with small beam

Coal devolatilization and char conversion under suspension fired conditions in O2/N2 and O2/CO2 atmospheres

DEFF Research Database (Denmark)

Jensen, Anker Degn; Brix, Jacob; Jensen, Peter Arendt

2010-01-01

have been carried out in an electrically heated entrained flow reactor that is designed to simulate the conditions in a suspension fired boiler. Coal devolatilized in N2 and CO2 atmospheres provided similar results regarding char morphology, char N2-BET surface area and volatile yield. This strongly......The aim of the present investigation is to examine differences between O2/N2 and O2/CO2 atmospheres during devolatilization and char conversion of a bituminous coal at conditions covering temperatures between 1173 K and 1673 K and inlet oxygen concentrations between 5 and 28 vol.%. The experiments...

Stable isotope ratios of the atmospheric CH4, CO2 and N2O in Tokai-mura

International Nuclear Information System (INIS)

Porntepkasemsan, Boonsom; Andoh, Mariko A.; Amano, Hikaru

2000-11-01

This report presents the results and interpretation of stable isotope ratios of the atmospheric CH 4 , CO 2 and N 2 O from a variety of sources in Tokai-mura. The seasonal changes of δ 13 CH 4 , δ 13 CO 2 and δ 15 N 2 O were determined under in-situ conditions in four sampling sites and one control site. Such measurements are expected to provide a useful means of estimating the transport mechanisms of the three trace gases in the environment. These isotopic signatures were analyzed by Isotope Ratio Mass Spectrometer (IRMS, Micromass Isoprime). Our data showed the significant seasonal fluctuation in the Hosoura rice paddy during the entire growing season in 1999. Possible causes for the variation are postulated. Additional measurements on soil properties and on organic δ 13 C in rice plant are suggested. Cited outstanding original papers are summarized in the references. (author)

Airborne 2-Micron Double-Pulsed Integrated Path Differential Absorption Lidar for Column CO2 Measurement

Science.gov (United States)

Singh, Upendra N.; Yu, Jirong; Petros, Mulugeta; Refaat, Tamer F.; Remus, Ruben G.; Fay, James J.; Reithmaier, Karl

2014-01-01

Double-pulse 2-micron lasers have been demonstrated with energy as high as 600 millijouls and up to 10 Hz repetition rate. The two laser pulses are separated by 200 microseconds and can be tuned and locked separately. Applying double-pulse laser in DIAL system enhances the CO2 measurement capability by increasing the overlap of the sampled volume between the on-line and off-line. To avoid detection complicity, integrated path differential absorption (IPDA) lidar provides higher signal-to-noise ratio measurement compared to conventional range-resolved DIAL. Rather than weak atmospheric scattering returns, IPDA rely on the much stronger hard target returns that is best suited for airborne platforms. In addition, the IPDA technique measures the total integrated column content from the instrument to the hard target but with weighting that can be tuned by the transmitter. Therefore, the transmitter could be tuned to weight the column measurement to the surface for optimum CO2 interaction studies or up to the free troposphere for optimum transport studies. Currently, NASA LaRC is developing and integrating a double-Pulsed 2-micron direct detection IPDA lidar for CO2 column measurement from an airborne platform. The presentation will describe the development of the 2-micron IPDA lidar system and present the airborne measurement of column CO2 and will compare to in-situ measurement for various ground target of different reflectivity.

Glacial-interglacial atmospheric CO2 change: a possible

Directory of Open Access Journals (Sweden)

L. C. Skinner

2009-09-01

Full Text Available So far, the exploration of possible mechanisms for glacial atmospheric CO2 drawdown and marine carbon sequestration has tended to focus on dynamic or kinetic processes (i.e. variable mixing-, equilibration- or export rates. Here an attempt is made to underline instead the possible importance of changes in the standing volumes of intra-oceanic carbon reservoirs (i.e. different water-masses in influencing the total marine carbon inventory. By way of illustration, a simple mechanism is proposed for enhancing the marine carbon inventory via an increase in the volume of relatively cold and carbon-enriched deep water, analogous to modern Lower Circumpolar Deep Water (LCDW, filling the ocean basins. A set of simple box-model experiments confirm the expectation that a deep sea dominated by an expanded LCDW-like watermass holds more CO2, without any pre-imposed changes in ocean overturning rate, biological export or ocean-atmosphere exchange. The magnitude of this "standing volume effect" (which operates by boosting the solubility- and biological pumps might be as large as the contributions that have previously been attributed to carbonate compensation, terrestrial biosphere reduction or ocean fertilisation for example. By providing a means of not only enhancing but also driving changes in the efficiency of the biological- and solubility pumps, this standing volume mechanism may help to reduce the amount of glacial-interglacial CO2 change that remains to be explained by other mechanisms that are difficult to assess in the geological archive, such as reduced mass transport or mixing rates in particular. This in turn could help narrow the search for forcing conditions capable of pushing the global carbon cycle between glacial and interglacial modes.

A terrestrial biosphere model optimized to atmospheric CO2 concentration and above ground woody biomass

Science.gov (United States)

Saito, M.; Ito, A.; Maksyutov, S. S.

2013-12-01

This study documents an optimization of a prognostic biosphere model (VISIT; Vegetation Integrative Similator for Trace gases) to observations of atmospheric CO2 concentration and above ground woody biomass by using a Bayesian inversion method combined with an atmospheric tracer transport model (NIES-TM; National Institute for Environmental Studies / Frontier Research Center for Global Change (NIES/FRCGC) off-line global atmospheric tracer transport model). The assimilated observations include 74 station records of surface atmospheric CO2 concentration and aggregated grid data sets of above ground woody biomass (AGB) and net primary productivity (NPP) over the globe. Both the biosphere model and the atmospheric transport model are used at a horizontal resolution of 2.5 deg x 2.5 deg grid with temporal resolutions of a day and an hour, respectively. The atmospheric transport model simulates atmospheric CO2 concentration with nine vertical levels using daily net ecosystem CO2 exchange rate (NEE) from the biosphere model, oceanic CO2 flux, and fossil fuel emission inventory. The models are driven by meteorological data from JRA-25 (Japanese 25-year ReAnalysis) and JCDAS (JMA Climate Data Assimilation System). Statistically optimum physiological parameters in the biosphere model are found by iterative minimization of the corresponding Bayesian cost function. We select thirteen physiological parameter with high sensitivity to NEE, NPP, and AGB for the minimization. Given the optimized physiological parameters, the model shows error reductions in seasonal variation of the CO2 concentrations especially in the northern hemisphere due to abundant observation stations, while errors remain at a few stations that are located in coastal coastal area and stations in the southern hemisphere. The model also produces moderate estimates of the mean magnitudes and probability distributions in AGB and NPP for each biome. However, the model fails in the simulation of the terrestrial

Regional scale variations of atmospheric CO2 and CH4 from satellite observation

International Nuclear Information System (INIS)

Ru, F; Lei, L; Guan, X; Bu, R; Qi, J

2014-01-01

To identify the sources, sinks and changes of atmospheric CO 2 and CH 4 , this study investigates the spatio-temporal changes of atmospheric CO 2 and CH 4 concentration on the regional scale by the satellite observations. In this paper, choosing the land region of China as the study area, we investigate the spatio-temporal changes of atmospheric CO 2 and CH 4 concentrations using the data of the CO 2 dry air mixing ratio (XCO 2 ), and the CH 4 dry air mixing ratio (XCH 4 ), retrieved by the Greenhouse Gases Observing Satellite (GOSAT) from Jan. 2010 to Dec. 2012. The results show that (1) both XCO 2 and XCH 4 show higher concentrations in southeastern regions than that in the northwestern, and tend to yearly increasing from 2010 to 2013; (2) XCO 2 shows obvious seasonal change with higher values in the spring than that in summer. The seasonal peak-to-peak amplitude is 8 ppm and the annual growth is about 2 ppm. XCH 4 , however, does not show a seasonal change; (3) With regard to different land-use backgrounds, XCO 2 shows larger concentrations over the areas of urban agglomeration than that over the grasslands and deserts, and XCH 4 shows lower concentrations over deserts than that over the Yangtze River Delta region and Sichuan Basin

Response of a tundra ecosystem to elevated atmospheric carbon dioxide and CO{sub 2}-induced climate change. Annual technical report

Energy Technology Data Exchange (ETDEWEB)

Oechel, W.C.

1993-02-01

Northern ecosystems contain up to 455 Gt of C in the soil active layer and upper permafrost, which is equivalent to approximately 60% of the carbon currently in the atmosphere as CO{sub 2}. Much of this carbon is stored in the soil as dead organic matter. Its fate is subject to the net effects of global change on the plant and soil systems of northern ecosystems. The arctic alone contains about 60 Gt C, 90% of which is present in the soil active layer and upper permafrost, and is assumed to have been a sink for CO{sub 2} during the historic and recent geologic past. Depending on the nature, rate, and magnitude of global environmental change, the arctic may have a positive or negative feedback on global change. Results from the DOE- funded research efforts of 1990 and 1991 indicate that the arctic has become a source of CO{sub 2} to the atmosphere. Measurements made in the Barrow, Alaska region during 1992 support these results. This change coincides with recent climatic variation in the arctic, and suggests a positive feedback of arctic ecosystems on atmospheric CO{sub 2} and global change. There are obvious potential errors in scaling plot level measurements to landscape, mesoscale, and global spatial scales. In light of the results from the recent DOE-funded research, and the remaining uncertainties regarding the change in arctic ecosystem function due to high latitude warming, a revised set of research goals is proposed for the 1993--94 year. The research proposed in this application has four principal aspects: (A) Long- term response of arctic plants and ecosystems to elevated atmospheric CO{sub 2}. (B) Circumpolar patterns of net ecosystem CO{sub 2} flux. (C) In situ controls by temperature and moisture on net ecosystem CO{sub 2} flux. (D) Scaling of CO{sub 2} flux from plot, to landscape, to regional scales.

Stable isotope measurement techniques for atmospheric greenhouse gases

International Nuclear Information System (INIS)

2002-01-01

The technical requirements to perform useful measurements of atmospheric greenhouse gas concentrations and of their isotope ratios are of direct relevance for all laboratories engaged in this field. A meaningful interpretation of isotopes in global models on sources and sinks of CO 2 and other greenhouse gases depends on strict laboratory protocols and data quality control measures ensuring comparable data in time and space. Only with this precondition met, the isotope techniques can serve as a potentially powerful method for reducing uncertainties in the global CO 2 budgets and for tracing pathways and interaction of terrestrial, oceanic, and atmospheric pools of carbon. This publication provides four contributions describing methods for the determination of the isotopic composition of trace gases in atmospheric air and in ice cores. These contributions have been indexed separately

Effect of atmospheric CO{sub 2} on surface segregation and phase formation in La{sub 0.6}Sr{sub 0.4}Co{sub 0.2}Fe{sub 0.8}O{sub 3−δ} thin films

Energy Technology Data Exchange (ETDEWEB)

Yu, Yang [Division of Materials Science and Engineering, Boston University, Brookline, MA 02446 (United States); Luo, Heng [Department of Mechanical Engineering, Boston University, Boston, MA 02215 (United States); Cetin, Deniz [Division of Materials Science and Engineering, Boston University, Brookline, MA 02446 (United States); Lin, Xi [Division of Materials Science and Engineering, Boston University, Brookline, MA 02446 (United States); Department of Mechanical Engineering, Boston University, Boston, MA 02215 (United States); Ludwig, Karl [Division of Materials Science and Engineering, Boston University, Brookline, MA 02446 (United States); Department of Physics, Boston University, Boston, MA 02215 (United States); Pal, Uday; Gopalan, Srikanth [Division of Materials Science and Engineering, Boston University, Brookline, MA 02446 (United States); Department of Mechanical Engineering, Boston University, Boston, MA 02215 (United States); Basu, Soumendra, E-mail: basu@bu.edu [Division of Materials Science and Engineering, Boston University, Brookline, MA 02446 (United States); Department of Mechanical Engineering, Boston University, Boston, MA 02215 (United States)

2014-12-30

Highlights: • LSCF exhibits Sr surface segregation on high-temperature annealing. • The presence of atmospheric CO{sub 2} enhances the kinetics of Sr surface segregation. • At high-CO{sub 2} partial pressures, there is a significant coverage of the surface by Sr-rich phases. • The increase in kinetics is attributed to increased thermodynamic driving force for SrCO{sub 3} formation. - Abstract: The effects of atmospheric CO{sub 2} on surface segregation and phase formation in La{sub 0.6}Sr{sub 0.4}Co{sub 0.2}Fe{sub 0.8}O{sub 3−δ} (LSCF-6428) were investigated. (0 0 1)-oriented LSCF-6428 thin films were deposited on lattice matched (1 1 0)-oriented NdGaO{sub 3} (NGO) substrates by pulsed laser deposition (PLD). Using the synchrotron technique of total reflection X-ray fluorescence (TXRF), it was found that the kinetics of Sr surface segregation was enhanced when annealing at 800 °C in a high-CO{sub 2} partial pressure, as compared to a similar anneal in a CO{sub 2}-free atmosphere, with the oxygen partial pressure being constant in both cases. Hard X-ray photoelectron spectroscopy (HAXPES) measurements showed that the contribution of the surface carbonate to surface oxide phases increased significantly for the sample annealed in the high-CO{sub 2} atmosphere. Atomic force microscopy (AFM) studies showed enhanced surface phase formation during the high-CO{sub 2} partial pressure anneal. Density functional theory (DFT) calculations provide a thermodynamic basis for the enhanced kinetics of surface segregation in the presence of atmospheric CO{sub 2}.

Six commercially viable ways to remove CO2 from the atmosphere and/or reduce CO2 emissions

NARCIS (Netherlands)

Schuiling, O.; de Boer, P.L.

2013-01-01

Background The burning of fossil fuels is the main cause of rising CO2 levels of the atmosphere. This will probably result in climate change. Another consequence is ocean acidification. Although these consequences are not yet proven beyond doubt, the risk of doing nothing is too large. The simplest

Biological and physical controls in the Southern Ocean on past millennial-scale atmospheric CO2 changes.