Sample records for absorb atmospheric co2

  1. Observational constraints on the global atmospheric CO2 budget

    NASA Technical Reports Server (NTRS)

    Tans, Pieter P.; Fung, Inez Y.; Takahashi, Taro

    1990-01-01

    Observed atmospheric concentrations of CO2 and data on the partial pressures of CO2 in surface ocean waters are combined to identify globally significant sources and sinks of CO2. The atmospheric data are compared with boundary layer concentrations calculated with the transport fields generated by a general circulation model (GCM) for specified source-sink distributions. In the model the observed north-south atmospheric concentration gradient can be maintained only if sinks for CO2 are greater in the Northern than in the Southern Hemisphere. The observed differences between the partial pressure of CO2 in the surface waters of the Northern Hemisphere and the atmosphere are too small for the oceans to be the major sink of fossil fuel CO2. Therefore, a large amount of the CO2 is apparently absorbed on the continents by terrestrial ecosystems.

  2. Different CO2 absorbents-modified SBA-15 sorbent for highly selective CO2 capture

    NASA Astrophysics Data System (ADS)

    Liu, Xiuwu; Zhai, Xinru; Liu, Dongyang; Sun, Yan

    2017-05-01

    Different CO2 absorbents-modified SBA-15 materials are used as CO2 sorbent to improve the selectivity of CH4/CO2 separation. The SBA-15 sorbents modified by physical CO2 absorbents are very limited to increasing CO2 adsorption and present poor selectivity. However, the SBA-15 sorbents modified by chemical CO2 absorbents increase CO2 adsorption capacity obviously. The separation coefficients of CO2/CH4 increase in this case. The adsorption and regeneration properties of the SBA-15 sorbents modified by TEA, MDEA and DIPA have been compared. The SBA-15 modified by triethanolamine (TEA) presents better CO2/CH4 separation performance than the materials modified by other CO2 absorbents.

  3. Improving CO2 permeation and separation performance of CO2-philic polymer membrane by blending CO2 absorbents

    NASA Astrophysics Data System (ADS)

    Cheng, Jun; Hu, Leiqing; Li, Yannan; Liu, Jianzhong; Zhou, Junhu; Cen, Kefa

    2017-07-01

    To research effects of CO2 absorption capacity and type of CO2 absorbent on the CO2 separation and free-volume properties of facilitated transport membranes, two types of CO2 absorbents, namely monoethanolamine (MEA) and ionic liquids (ILs:[P66614][Triz] and [P66614][2-Op]), were adopted. The CO2 absorption capacities of MEA, [P66614][Triz] and [P66614][2-Op] were about 0.561 mol CO2 per mol, 0.95 mol CO2 per mol and 1.60 mol CO2 per mol, respectively. All mean free-volume hole radiuses of membranes decreased after blending CO2 absorbents. After polymer membrane blended with two ILs, number of free-volume hole increased, resulting in modest increase of the fractional free volume. Both CO2 permeability and selectivity increased after blending MEA and ILs. The increasing range of CO2 permeability corresponded with CO2 absorption capacity of CO2 absorbents, and membrane blending with [P66614][2-Op] showed the highest CO2 permeability of 672.1 Barrers at 25 °C. Pebax/PEGDME membrane blending with MEA obtained the highest CO2/H2 and CO2/CH4 selectivity at 17.8 and 20.5, respectively.

  4. A Global Perspective of Atmospheric CO2 Concentrations

    NASA Technical Reports Server (NTRS)

    Putman, William M.; Ott, Lesley; Darmenov, Anton; daSilva, Arlindo

    2016-01-01

    Carbon dioxide (CO2) is the most important greenhouse gas affected by human activity. About half of the CO2 emitted from fossil fuel combustion remains in the atmosphere, contributing to rising temperatures, while the other half is absorbed by natural land and ocean carbon reservoirs. Despite the importance of CO2, many questions remain regarding the processes that control these fluxes and how they may change in response to a changing climate. The Orbiting Carbon Observatory-2 (OCO-2), launched on July 2, 2014, is NASA's first satellite mission designed to provide the global view of atmospheric CO2 needed to better understand both human emissions and natural fluxes. This visualization shows how column CO2 mixing ratio, the quantity observed by OCO-2, varies throughout the year. By observing spatial and temporal gradients in CO2 like those shown, OCO-2 data will improve our understanding of carbon flux estimates. But, CO2 observations can't do that alone. This visualization also shows that column CO2 mixing ratios are strongly affected by large-scale weather systems. In order to fully understand carbon flux processes, OCO-2 observations and atmospheric models will work closely together to determine when and where observed CO2 came from. Together, the combination of high-resolution data and models will guide climate models towards more reliable predictions of future conditions.

  5. CO2 greenhouse in the early martian atmosphere: SO2 inhibits condensation

    NASA Technical Reports Server (NTRS)

    Yung, Y. L.; Nair, H.; Gerstell, M. F.

    1997-01-01

    Many investigators of the early martian climate have suggested that a dense carbon dioxide atmosphere was present and warmed the surface above the melting point of water (J.B. Pollack, J.F. Kasting, S.M. Richardson, and K. Poliakoff 1987. Icarus 71, 203-224). However, J.F. Kasting (1991. Icarus 94, 1-13) pointed out that previous thermal models of the primitive martian atmosphere had not considered the condensation of CO2. When this effect was incorporated, Kasting found that CO2 by itself is inadequate to warm the surface. SO2 absorbs strongly in the near UV region of the solar spectrum. While a small amount of SO2 may have a negligible effect by itself on the surface temperature, it may have significantly warmed the middle atmosphere of early Mars, much as ozone warms the terrestrial stratosphere today. If this region is kept warm enough to inhibit the condensation of CO2, then CO2 remains a viable greenhouse gas. Our preliminary radiative modeling shows that the addition of 0.1 ppmv of SO2 in a 2 bar CO2 atmosphere raises the temperature of the middle atmosphere by approximately 10 degrees, so that the upper atmosphere in a 1 D model remains above the condensation temperature of CO2. In addition, this amount of SO2 in the atmosphere provides an effective UV shield for a hypothetical biosphere on the martian surface.

  6. Liquid water on Mars - an energy balance climate model for CO2/H2O atmospheres

    NASA Astrophysics Data System (ADS)

    Hoffert, M. I.; Callegari, A. J.; Hsieh, T.; Ziegler, W.

    1981-07-01

    A simple climatic model is developed for a Mars atmosphere containing CO2 and sufficient liquid water to account for the observed hydrologic surface features by the existence of a CO2/H2O greenhouse effect. A latitude-resolved climate model originally devised for terrestrial climate studies is applied to Martian conditions, with the difference between absorbed solar flux and emitted long-wave flux to space per unit area attributed to the divergence of the meridional heat flux and the poleward heat flux assumed to equal the atmospheric eddy heat flux. The global mean energy balance is calculated as a function of atmospheric pressure to assess the CO2/H2O greenhouse liquid water hypothesis, and some latitude-resolved cases are examined in detail in order to clarify the role of atmospheric transport and temperature-albedo feedback. It is shown that the combined CO2/H2O greenhouse at plausible early surface pressures may account for climates hot enough to support a hydrological cycle and running water at present-day insolation and visible albedo levels.

  7. Liquid water on Mars - An energy balance climate model for CO2/H2O atmospheres

    NASA Technical Reports Server (NTRS)

    Hoffert, M. I.; Callegari, A. J.; Hsieh, C. T.; Ziegler, W.

    1981-01-01

    A simple climatic model is developed for a Mars atmosphere containing CO2 and sufficient liquid water to account for the observed hydrologic surface features by the existence of a CO2/H2O greenhouse effect. A latitude-resolved climate model originally devised for terrestrial climate studies is applied to Martian conditions, with the difference between absorbed solar flux and emitted long-wave flux to space per unit area attributed to the divergence of the meridional heat flux and the poleward heat flux assumed to equal the atmospheric eddy heat flux. The global mean energy balance is calculated as a function of atmospheric pressure to assess the CO2/H2O greenhouse liquid water hypothesis, and some latitude-resolved cases are examined in detail in order to clarify the role of atmospheric transport and temperature-albedo feedback. It is shown that the combined CO2/H2O greenhouse at plausible early surface pressures may account for climates hot enough to support a hydrological cycle and running water at present-day insolation and visible albedo levels.

  8. CO2 Dissociation using the Versatile Atmospheric Dielectric Barrier Discharge Experiment (VADER)

    NASA Astrophysics Data System (ADS)

    Lindon, Michael Allen

    As of 2013, the Carbon Dioxide Information Analysis Center (CDIAC) estimates that the world emits approximately 36 trillion metric tons of Carbon Dioxide (CO2) into the atmosphere every year. These large emissions have been correlated to global warming trends that have many consequences across the globe, including glacial retraction, ocean acidification and increased severity of weather events. With green technologies still in the infancy stage, it can be expected that CO2 emissions will stay this way for along time to come. Approximately 41% of the emissions are due to electricity production, which pump out condensed forms of CO2. This danger to our world is why research towards new and innovative ways of controlling CO2 emissions from these large sources is necessary. As of now, research is focused on two primary methods of CO2 reduction from condensed CO2 emission sources (like fossil fuel power plants): Carbon Capture and Sequestration (CCS) and Carbon Capture and Utilization (CCU). CCS is the process of collecting CO2 using absorbers or chemicals, extracting the gas from those absorbers and finally pumping the gas into reservoirs. CCU on the other hand, is the process of reacting CO2 to form value added chemicals, which can then be recycled or stored chemically. A Dielectric Barrier discharge (DBD) is a pulsed, low temperature, non-thermal, atmospheric pressure plasma which creates high energy electrons suitable for dissociating CO2 into its components (CO and O) as one step in the CCU process. Here I discuss the viability of using a DBD for CO2 dissociation on an industrial scale as well as the fundamental physics and chemistry of a DBD for CO2 dissociation. This work involved modeling the DBD discharge and chemistry, which showed that there are specific chemical pathways and plasma parameters that can be adjusted to improve the CO2 reaction efficiencies and rates. Experimental studies using the Versatile Atmospheric dielectric barrier Discharge Expe

  9. Do Continental Shelves Act as an Atmospheric CO2 Sink?

    NASA Astrophysics Data System (ADS)

    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.

  10. Influence of the concentration of CO2 and SO2 on the absorption of CO2 by a lithium orthosilicate-based absorbent.

    PubMed

    Pacciani, R; Torres, J; Solsona, P; Coe, C; Quinn, R; Hufton, J; Golden, T; Vega, L F

    2011-08-15

    A novel, high temperature solid absorbent based on lithium orthosilicate (Li(4)SiO(4)) has shown promise for postcombustion CO(2) capture. Previous studies utilizing a clean, synthetic flue gas have shown that the absorbent has a high CO(2) capacity, >25 wt %, along with high absorption rates, lower heat of absorption and lower regeneration temperature than other solids such as calcium oxide. The current effort was aimed at evaluating the Li(4)SiO(4) based absorbent in the presence of contaminants found in typical flue gas, specifically SO(2), by cyclic exposure to gas mixtures containing CO(2), H(2)O (up to 25 vol. %), and SO(2) (up to 0.95 vol. %). In the absence of SO(2), a stable CO(2) capacity of ∼ 25 wt % over 25 cycles at 550 °C was achieved. The presence of SO(2), even at concentrations as low as 0.002 vol. %, resulted in an irreversible reaction with the absorbent and a decrease in CO(2) capacity. Analysis of SO(2)-exposed samples revealed that the absorbent reacted chemically and irreversibly with SO(2) at 550 °C forming Li(2)SO(4). Thus, industrial application would require desulfurization of flue gas prior to contacting the absorbent. Reactivity with SO(2) is not unique to the lithium orthosilicate material, so similar steps would be required for other absorbents that chemically react with SO(2).

  11. In vitro performance of prefilled CO2 absorbers with the Zeus®.

    PubMed

    Omer, Mohab; Hendrickx, Jan F A; De Ridder, Simon; De Houwer, Alexander; Carette, Rik; De Cooman, Sofie; De Wolf, Andre M

    2017-12-13

    Low fresh gas flows (FGFs) decrease the use of anesthetic gases, but increase CO 2 absorbent usage. CO 2 absorbent usage remains poorly quantified. The goal of this study is to determine canister life of 8 commercially available CO 2 absorbent prepacks with the Zeus ® . Pre-packed CO 2 canisters of 8 different brands were tested in vitro: Amsorb Plus, Spherasorb, LoFloSorb, LithoLyme, SpiraLith, SpheraSorb, Drägersorb 800+, Drägersorb Free, and CO2ntrol. CO 2 (160 mL min - 1 ) flowed into the tip of a 2 L breathing bag that was ventilated with a tidal volume of 500 mL, a respiratory rate of 10/min, and an I:E ratio of 1:1 using the controlled mechanical ventilation mode of the Zeus ® (Dräger, Lubeck, Germany). In part I, canister life of 5 canisters each of 2 different lots of each brand was determined with a 350 mL min - 1 FGF. Canister life is the time it takes for the inspired CO 2 concentration (F I CO 2 ) to rise to 0.5%. In part II, canister life was measured accross a FGF range of 0.25 to 4 L min - 1 for Drägersorb 800+ (2 lots) and SpiraLith (1 lot). In part III, the calculated canister life per 100 g fresh granule content of the different brands was compared between the Zeus and (previously published data for) the Aisys. In vitro canister life of prefilled CO 2 absorber canisters differed between brands, and depended on the amount of CO 2 absorbent and chemical composition. Canister life expressed as FCU 0.5 (the fraction of the canister used per hour) was proportional to FGF over 0.2-2 L min -1 range only, but was non-linear with higher FGF: FCU 0.5 was larger than expected with FGF > 2 L min -1 , and even with FGF > minute ventilation FCU 0.5 did not become zero, indicating some CO 2 was being absorbed. Canister life on a per weight basis of the same brand is higher with the Zeus than the Aisys. Canister life of prefilled CO 2 absorber canisters differs between brands. The FCU 0.5 -FGF relationship is not linear across

  12. Why CO2 cools the middle atmosphere - a consolidating model perspective

    NASA Astrophysics Data System (ADS)

    Goessling, Helge F.; Bathiany, Sebastian

    2016-08-01

    Complex models of the atmosphere show that increased carbon dioxide (CO2) concentrations, while warming the surface and troposphere, lead to lower temperatures in the stratosphere and mesosphere. This cooling, which is often referred to as "stratospheric cooling", is evident also in observations and considered to be one of the fingerprints of anthropogenic global warming. Although the responsible mechanisms have been identified, they have mostly been discussed heuristically, incompletely, or in combination with other effects such as ozone depletion, leaving the subject prone to misconceptions. Here we use a one-dimensional window-grey radiation model of the atmosphere to illustrate the physical essence of the mechanisms by which CO2 cools the stratosphere and mesosphere: (i) the blocking effect, associated with a cooling due to the fact that CO2 absorbs radiation at wavelengths where the atmosphere is already relatively opaque, and (ii) the indirect solar effect, associated with a cooling in places where an additional (solar) heating term is present (which on Earth is particularly the case in the upper parts of the ozone layer). By contrast, in the grey model without solar heating within the atmosphere, the cooling aloft is only a transient blocking phenomenon that is completely compensated as the surface attains its warmer equilibrium. Moreover, we quantify the relative contribution of these effects by simulating the response to an abrupt increase in CO2 (and chlorofluorocarbon) concentrations with an atmospheric general circulation model. We find that the two permanent effects contribute roughly equally to the CO2-induced cooling, with the indirect solar effect dominating around the stratopause and the blocking effect dominating otherwise.

  13. Kinetic analysis of an anion exchange absorbent for CO2 capture from ambient air.

    PubMed

    Shi, Xiaoyang; Li, Qibin; Wang, Tao; Lackner, Klaus S

    2017-01-01

    This study reports a preparation method of a new moisture swing sorbent for CO2 capture from air. The new sorbent components include ion exchange resin (IER) and polyvinyl chloride (PVC) as a binder. The IER can absorb CO2 when surrounding is dry and release CO2 when surrounding is wet. The manuscript presents the studies of membrane structure, kinetic model of absorption process, performance of desorption process and the diffusivity of water molecules in the CO2 absorbent. It has been proved that the kinetic performance of CO2 absorption/desorption can be improved by using thin binder and hot water treatment. The fast kinetics of P-100-90C absorbent is due to the thin PVC binder, and high diffusion rate of H2O molecules in the sample. The impressive is this new CO2 absorbent has the fastest CO2 absorption rate among all absorbents which have been reported by other up-to-date literatures.

  14. Kinetic analysis of an anion exchange absorbent for CO2 capture from ambient air

    PubMed Central

    Shi, Xiaoyang; Li, Qibin; Lackner, Klaus S.

    2017-01-01

    This study reports a preparation method of a new moisture swing sorbent for CO2 capture from air. The new sorbent components include ion exchange resin (IER) and polyvinyl chloride (PVC) as a binder. The IER can absorb CO2 when surrounding is dry and release CO2 when surrounding is wet. The manuscript presents the studies of membrane structure, kinetic model of absorption process, performance of desorption process and the diffusivity of water molecules in the CO2 absorbent. It has been proved that the kinetic performance of CO2 absorption/desorption can be improved by using thin binder and hot water treatment. The fast kinetics of P-100-90C absorbent is due to the thin PVC binder, and high diffusion rate of H2O molecules in the sample. The impressive is this new CO2 absorbent has the fastest CO2 absorption rate among all absorbents which have been reported by other up-to-date literatures. PMID:28640914

  15. [Study of new blended chemical absorbents to absorb CO2].

    PubMed

    Wang, Jin-Lian; Fang, Meng-Xiang; Yan, Shui-Ping; Luo, Zhong-Yang; Cen, Ke-Fa

    2007-11-01

    Three kinds of blended absorbents were investigated on bench-scale experimental bench according to absorption rate and regeneration grade to select a reasonable additive concentration. The results show that, among methyldiethanolamine (MDEA) and piperazine (PZ) mixtures, comparing MDEA : PZ = 1 : 0.4 (m : m) with MDEA : PZ = 1 : 0.2 (m : m), the absorption rate is increased by about 70% at 0.2 mol x mol(-1). When regeneration lasting for 40 min, regeneration grade of blended absorbents with PZ concentration of 0.2, 0.4, and 0.8 is decreased to 83.06%, 77.77% and 76.67% respectively while 91.04% for PZ concentration of 0. MDEA : PZ = 1 : 0.4(m : m) is a suitable ratio for MDEA/PZ mixtures as absorption and regeneration properties of the blended absorbents are all improved. The aqueous blends with 10% primary amines and 2% tertiary amines could keep high CO2 absorption rate, and lower regeneration energy consumption. Adding 2% 2-Amino-2-methyl-1-propanol (AMP) to 10% diethanolamine (DEA), the blended amine solvents have an advantage in absorption and regeneration properties over other DEA/AMP mixtures. Blended solvents, which consist of a mixture of primary amines with a small amount of tertiary amines, have the highest absorption rate among the three. And mixed absorbents of secondary amines and a small amount of sterically hindered amines have the best regeneration property. To combine absorption and regeneration properties, blends with medium activator addition to tertiary amines are competitive.

  16. CO2 Ice Formation and CO2 Gas Depletion in the Polar Winter Atmosphere of Mars from Mars Climate Sounder Measurements

    NASA Astrophysics Data System (ADS)

    Kleinboehl, A.; Patel, P. K.; Schofield, J. T.; Kass, D. M.; Hayne, P. O.; McCleese, D. J.

    2016-12-01

    Temperatures in the martian lower atmosphere commonly reach the frost point of CO2 in the polar winter vortices over an extended vertical range. New retrievals from the Mars Climate Sounder (MCS) instrument on Mars Reconnaissance Orbiter allow the characterization of the winter polar regions with improved accuracy. MCS is a passive infrared sounder with 5 mid-infrared, 3 far infrared, and one broadband visible/near-infrared channels. Each spectral channel uses a linear detector array consisting of 21 elements, which provides -10 to 90 km altitude coverage when pointed at the Mars limb. From the infrared measurements, vertical profiles of temperature and aerosols are retrieved with an altitude resolution of about 5 km. Due to their long optical path through the atmosphere, limb measurements are susceptible to horizontal gradients in temperature or absorber amount in their line-of-sight, an effect that is particularly important in polar winter regions due to strong latitudinal temperature gradients in the atmosphere. The new retrievals take horizontal gradients in temperature and aerosols into account by means of a two-dimensional radiative transfer scheme. The resulting temperature profiles reveal that temperatures in the south winter polar region repeatedly drop several degrees below the frost point of CO2. This behavior is consistent with the removal of CO2 from the atmosphere through condensation, resulting in an atmosphere that is depleted in gaseous CO2 and enhanced in non-condensable gases like N2 and Ar. In these regions emission features at 22 μm are often found in MCS limb measurements, consistent with the presence of CO2 ice in the polar vortex. We will map these depletions of CO2 gas and show correlations with the occurrence of CO2 ice. We will provide comparisons of these effects between the southern and the northern polar winter vortices.

  17. Atmospheric CO2 capture for the artificial photosynthetic system.

    PubMed

    Nogalska, Adrianna; Zukowska, Adrianna; Garcia-Valls, Ricard

    2018-04-15

    The aim of these studies is to evaluate the ambient CO 2 capture abilities of the membrane contactor system in the same conditions as leafs, such as ambient temperature, pressure and low CO 2 concentration, where the only driving force is the concentration gradient. The polysulfone membrane employed was made by a phase inversion process and characterized by ESEM micrographs which were used to determine the thickness, asymmetry and pore size. Besides, the porosity of the membrane was measured from the membrane and polysulfone density correlation and the hydrophobicity was analyzed by contact angle measurements. Moreover, the compatibility of membrane and absorbent was evaluated, in order to exclude wetting issues by meaning of swelling, dynamic contact angle and AFM analysis. The prepared membranes were introduced into a cross flow module and used as contactors between CO 2 and the absorbing media, a potassium hydroxide solution. The influence of the membrane thickness, absorbent stirring rate, solution pH and absorption time on CO 2 capture were evaluated. Absorbent solution stirring rate showed no statistically significant influence on absorption. We observed a non-linear correlation between the capture rate and the increase of absorbent solution pH as well as absorption time. The results showed that the efficiency of our CO 2 capture system is similar to stomatal carbon dioxide assimilation rate, achieving stable value of 20μmol/m 2 ·s after 1h of experiment. Copyright © 2017 Elsevier B.V. All rights reserved.

  18. Atmospheric inversion of the surface CO2 flux with 13CO2 constraint

    NASA Astrophysics Data System (ADS)

    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.

  19. Monitoring Atmospheric CO2 From Space: Challenge & Approach

    NASA Technical Reports Server (NTRS)

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

    2015-01-01

    Atmospheric CO2 is the key radiative forcing for the Earth's climate and may contribute a major part of the Earth's warming during the past 150 years. Advanced knowledge on the CO2 distributions and changes can lead considerable model improvements in predictions of the Earth's future climate. Large uncertainties in the predictions have been found for decades owing to limited CO2 observations. To obtain precise measurements of atmospheric CO2, certain challenges have to be overcome. For an example, global annual means of the CO2 are rather stable, but, have a very small increasing trend that is significant for multi-decadal long-term climate. At short time scales (a second to a few hours), regional and subcontinental gradients in the CO2 concentration are very small and only in an order of a few parts per million (ppm) compared to the mean atmospheric CO2 concentration of about 400 ppm, which requires atmospheric CO2 space monitoring systems with extremely high accuracy and precision (about 0.5 ppm or 0.125%) in spatiotemporal scales around 75 km and 10-s. It also requires a decadal-scale system stability. Furthermore, rapid changes in high latitude environments such as melting ice, snow and frozen soil, persistent thin cirrus clouds in Amazon and other tropical areas, and harsh weather conditions over Southern Ocean all increase difficulties in satellite atmospheric CO2 observations. Space lidar approaches using Integrated Path Differential Absorption (IPDA) technique are considered to be capable of obtaining precise CO2 measurements and, thus, have been proposed by various studies including the 2007 Decadal Survey (DS) of the U.S. National Research Council. This study considers to use the Intensity-Modulated Continuous-Wave (IM-CW) lidar to monitor global atmospheric CO2 distribution and variability from space. Development and demonstration of space lidar for atmospheric CO2 measurements have been made through joint adventure of NASA Langley Research Center and

  20. Atmospheric CO2 capture for the artificial photosynthetic system

    NASA Astrophysics Data System (ADS)

    Nogalska, Adrianna; Zukowska, Adrianna; Garcia-Valls, Ricard

    2017-11-01

    The scope of these studies is to evaluate the ambient CO2 capture abilities of the membrane contactor system in the same conditions as leaves works during photosynthesis, such as ambient temperature, pressure and low CO2 concentration, where the only driving force is the concentration gradient. The polysulfone membrane was made by phase inversion process and characterized by ESEM micrographs which were used to determine the thickness, asymmetry and pore size. Besides, the porosity of the membrane was measured from the membrane and polysulfone density correlation and hydrophobicity was analyzed by contact angle measurements. Moreover, the compatibility of the membrane and absorbent solution was evaluated, in order to exclude wetting issues. The prepared membranes were introduced in a cross flow module and used as contactor between the CO2 and the potassium hydroxide solution, as absorbing media. The influence of the membrane thickness, absorbent stirring rate and absorption time, on CO2 capture were evaluated. The results show that the efficiency of our CO2 capture system is similar to stomatal carbon dioxide assimilation rate.

  1. What is the main driver of atmospheric CO2 dynamic: ocean or permafrost?

    NASA Astrophysics Data System (ADS)

    Zimov, S. A.; Zimov, N.

    2010-12-01

    Majority have assumed that during the Last Deglaciation (LD) ocean was a strong source of carbon (C) transporting hundreds of gigatons of C into the terrestrial and atmospheric storages. Increase in the δ13C of foraminifera shells during the LD by 0.3-0.4 per mil considered as an evidence of such a source. However terrestrial and oceanic branches of the biological carbon cycle have very similar carbon isotopic signatures and carbon storage capacities. So the same δ13C increase could be caused by an oceanic bio-productivity increase and the increase of C in bottom sediments (Brovkin et al. 2002). Additionally it has been shown experimentally that at 90 ppmv increase in atmospheric CO2, due to changes in the concentration of carbonate ions in sea water, would cause the δ13C of foraminifera shells to increase by at least 0.25-0.5 per mil (Spero et al. 1997). At all stable parameters to equilibrate for 90 ppm CO2 increase in the atmosphere ocean inorganic C reservoir should have increased by 1800 Gt C (Sigman et al. 2000). Therefore it is very hard to find a mechanism which would allow ocean in LD to release carbon instead of absorbing it, and such a mechanism haven’t been found so far. Methane (CH4) produced by steppe-tundra biome (ST) soil thawing has a unique isotopic signal depleted in all isotopes. Inclusion of this source into a model of the atmospheric methane isotope budget allowed us to reconstruct the dynamics of methane’s main sources. Results indicated that thawing of ST soils during the deglaciation, were the largest methane source and resulted in 255 Gt C emitted in the form of CH4 to the atmosphere (Zimov, see AGU 2010). When soil turns anaerobic only minor portion of soil C converts into CH4. Bigger portion of ST didn’t turn anaerobic at all and all decomposing C was turned into CO2. Besides that part of the soil CH4 flux was consumed by methanotrophs. Therefore C storage in ST soils were many times higher then CH4 emission into the atmosphere

  2. Synthesis, characterization and field evaluation of a new calcium-based CO2 absorbent for radial diffusive sampler

    NASA Astrophysics Data System (ADS)

    Cucciniello, Raffaele; Proto, Antonio; Alfano, Davide; Motta, Oriana

    2012-12-01

    In this paper the use of passive sampling as a powerful approach to monitor atmospheric CO2 is assessed. Suitable substrate based on calcium-aluminium oxide was synthetized according to a process which permits to control the particle size of the CaO/Al based sorbent. The study shows that hydration of substrate is an essential part of the process of CO2 absorption and subsequent conversion to carbonate. X-ray diffraction, thermogravimetric analysis, environmental scanning electron microscopic analysis were used in order to characterize the substrate and to establish the best performances both in terms of particle size and CO2 absorption capacity. Passive samplers for CO2 monitoring were prepared and then tested at laboratory level and in the atmospheric environment. Validation was performed by comparison with an infrared continuous detector. Thermogravimetric analysis results, carried out to evaluate the absorbing capability of this new passive device, were in accordance with data collected at the same time by the active continuous analyser. The diffusive sampling rate and the diffusion coefficient of CO2 respect to this new passive device were also evaluated resulting equal to 47 ± 3 ml min-1 and 0.0509 ± 0.005 cm2 s-1, respectively.

  3. Estimating lake-atmosphere CO2 exchange

    USGS Publications Warehouse

    Anderson, D.E.; Striegl, Robert G.; Stannard, D.I.; Michmerhuizen, C.M.; McConnaughey, T.A.; LaBaugh, J.W.

    1999-01-01

    Lake-atmosphere CO2 flux was directly measured above a small, woodland lake using the eddy covariance technique and compared with fluxes deduced from changes in measured lake-water CO2 storage and with flux predictions from boundary-layer and surface-renewal models. Over a 3-yr period, lake-atmosphere exchanges of CO2 were measured over 5 weeks in spring, summer, and fall. Observed springtime CO2 efflux was large (2.3-2.7 ??mol m-2 s-1) immediately after lake-thaw. That efflux decreased exponentially with time to less than 0.2 ??mol m-2 s-1 within 2 weeks. Substantial interannual variability was found in the magnitudes of springtime efflux, surface water CO2 concentrations, lake CO2 storage, and meteorological conditions. Summertime measurements show a weak diurnal trend with a small average downward flux (-0.17 ??mol m-2 s-1) to the lake's surface, while late fall flux was trendless and smaller (-0.0021 ??mol m-2 s-1). Large springtime efflux afforded an opportunity to make direct measurement of lake-atmosphere fluxes well above the detection limits of eddy covariance instruments, facilitating the testing of different gas flux methodologies and air-water gas-transfer models. Although there was an overall agreement in fluxes determined by eddy covariance and those calculated from lake-water storage change in CO2, agreement was inconsistent between eddy covariance flux measurements and fluxes predicted by boundary-layer and surface-renewal models. Comparison of measured and modeled transfer velocities for CO2, along with measured and modeled cumulative CO2 flux, indicates that in most instances the surface-renewal model underpredicts actual flux. Greater underestimates were found with comparisons involving homogeneous boundary-layer models. No physical mechanism responsible for the inconsistencies was identified by analyzing coincidentally measured environmental variables.

  4. Influence of the biosphere and circulation on atmospheric CO2

    NASA Astrophysics Data System (ADS)

    Corbett, A.; Jiang, X.; La, J.; Olsen, E. T.; Licata, S. J.; Yung, Y. L.

    2017-12-01

    Using multiple satellite CO2 retrievals (e.g., AIRS, GOSAT, and OCO-2), we have investigated seasonal changes of CO2 as a function of latitudes and altitudes. The annual cycle of atmospheric CO2 is closely related to the exchange of CO2 between the biosphere and the atmosphere, so we also examine solar-induced fluorescence (SIF). High SIF value means more CO2 uptake by photosynthesis, which will lead to lower atmospheric CO2 concentrations. The satellite data demonstrate a negative correlation between atmospheric CO2 and SIF. SIF can be influenced by precipitation and evaporation. We have found a positive correlation between SIF and the difference of precipitation and evaporation, suggesting there is more CO2 uptake by vegetation when more water is available. In addition to the annual cycle, large-scale circulation, such as South Atlantic Walker Circulation, can also modulate atmospheric CO2 concentrations. As seen from AIRS, GOSAT, and OCO-2 CO2 retrievals, there is less CO2 over the South Atlantic Ocean than over South America from December to March. Results in this study will help us better understand interactions between the biosphere, circulation, and atmospheric CO2.

  5. Decadal trends in regional CO2 fluxes estimated from atmospheric inversions

    NASA Astrophysics Data System (ADS)

    Saeki, T.; Patra, P. K.

    2016-12-01

    Top-down approach (or atmospheric inversion) using atmospheric transport models and CO2 observations are an effective way to optimize surface fluxes at subcontinental scales and monthly time intervals. We used the CCSR/NIES/FRCGC AGCM-based Chemistry Transport Model (JAMSTEC's ACTM) and atmospheric CO2 concentrations at NOAA, CSIRO, JMA, NIES, NIES-MRI sites from Obspack GLOBALVIEW-CO2 data product (2013) for estimating CO2 fluxes for the period of 1990-2011. Carbon fluxes were estimated for 84 partitions (54 lands + 30 oceans) of the globe by using a Bayesian synthesis inversion framework. A priori fluxes are (1) atmosphere-ocean exchange from Takahashi et al. (2009), (2) 3-hourly terrestrial biosphere fluxes (annually balanced) from CASA model, and (3) fossil fuel fluxes from CDIAC global totals and EDGAR4.2 spatial distributions. Four inversion cases have been tested with 1) 21 sites (sites which have real data fraction of 90 % or more for 1989-2012), 2) 21 sites + CONTRAIL data, 3) 66 sites (over 70 % coverage), and 4) 157 sites. As a result of time-dependent inversions, mean total flux (excluding fossil fuel) for the period 1990-2011 is estimated to be -3.09 ±0.16 PgC/yr (mean and standard deviation of the four cases), where land (incl. biomass burning and land use change) and ocean absorb an average rate of -1.80 ±0.18 and -1.29 ±0.08 PgC/yr, respectively. The average global total sink from 1991-2000 to 2001-2010 increases by about 0.5 PgC/yr, mainly due to the increase in northern and tropical land sinks (Africa, Boreal Eurasia, East Asia and Europe), while ocean sinks show no clear trend. Inversion with CONTRAIL data estimates large positive flux anomalies in late 1997 associated with the 1997/98 El-Nino, while inversion without CONTARIL data between Japan and Australia fails to estimate such large anomalies. Acknowledgements. This work is supported by the Environment Research and Technology Development Fund (2-1401) of the Ministry of the Environment

  6. Biomass fast pyrolysis in a fluidized bed reactor under N2, CO2, CO, CH4 and H2 atmospheres.

    PubMed

    Zhang, Huiyan; Xiao, Rui; Wang, Denghui; He, Guangying; Shao, Shanshan; Zhang, Jubing; Zhong, Zhaoping

    2011-03-01

    Biomass fast pyrolysis is one of the most promising technologies for biomass utilization. In order to increase its economic potential, pyrolysis gas is usually recycled to serve as carrier gas. In this study, biomass fast pyrolysis was carried out in a fluidized bed reactor using various main pyrolysis gas components, namely N(2), CO(2), CO, CH(4) and H(2), as carrier gases. The atmosphere effects on product yields and oil fraction compositions were investigated. Results show that CO atmosphere gave the lowest liquid yield (49.6%) compared to highest 58.7% obtained with CH(4). CO and H(2) atmospheres converted more oxygen into CO(2) and H(2)O, respectively. GC/MS analysis of the liquid products shows that CO and CO(2) atmospheres produced less methoxy-containing compounds and more monofunctional phenols. The higher heating value of the obtained bio-oil under N(2) atmosphere is only 17.8 MJ/kg, while that under CO and H(2) atmospheres increased to 23.7 and 24.4 MJ/kg, respectively. Copyright © 2010 Elsevier Ltd. All rights reserved.

  7. Constraining terrestrial ecosystem CO2 fluxes by integrating models of biogeochemistry and atmospheric transport and data of surface carbon fluxes and atmospheric CO2 concentrations

    NASA Astrophysics Data System (ADS)

    Zhu, Q.; Zhuang, Q.; Henze, D.; Bowman, K.; Chen, M.; Liu, Y.; He, Y.; Matsueda, H.; Machida, T.; Sawa, Y.; Oechel, W.

    2014-09-01

    Regional net carbon fluxes of terrestrial ecosystems could be estimated with either biogeochemistry models by assimilating surface carbon flux measurements or atmospheric CO2 inversions by assimilating observations of atmospheric CO2 concentrations. Here we combine the ecosystem biogeochemistry modeling and atmospheric CO2 inverse modeling to investigate the magnitude and spatial distribution of the terrestrial ecosystem CO2 sources and sinks. First, we constrain a terrestrial ecosystem model (TEM) at site level by assimilating the observed net ecosystem production (NEP) for various plant functional types. We find that the uncertainties of model parameters are reduced up to 90% and model predictability is greatly improved for all the plant functional types (coefficients of determination are enhanced up to 0.73). We then extrapolate the model to a global scale at a 0.5° × 0.5° resolution to estimate the large-scale terrestrial ecosystem CO2 fluxes, which serve as prior for atmospheric CO2 inversion. Second, we constrain the large-scale terrestrial CO2 fluxes by assimilating the GLOBALVIEW-CO2 and mid-tropospheric CO2 retrievals from the Atmospheric Infrared Sounder (AIRS) into an atmospheric transport model (GEOS-Chem). The transport inversion estimates that: (1) the annual terrestrial ecosystem carbon sink in 2003 is -2.47 Pg C yr-1, which agrees reasonably well with the most recent inter-comparison studies of CO2 inversions (-2.82 Pg C yr-1); (2) North America temperate, Europe and Eurasia temperate regions act as major terrestrial carbon sinks; and (3) The posterior transport model is able to reasonably reproduce the atmospheric CO2 concentrations, which are validated against Comprehensive Observation Network for TRace gases by AIrLiner (CONTRAIL) CO2 concentration data. This study indicates that biogeochemistry modeling or atmospheric transport and inverse modeling alone might not be able to well quantify regional terrestrial carbon fluxes. However, combining

  8. Strengthening seasonal marine CO2 variations due to increasing atmospheric CO2

    NASA Astrophysics Data System (ADS)

    Landschützer, Peter; Gruber, Nicolas; Bakker, Dorothee C. E.; Stemmler, Irene; Six, Katharina D.

    2018-01-01

    The increase of atmospheric CO2 (ref. 1) has been predicted to impact the seasonal cycle of inorganic carbon in the global ocean2,3, yet the observational evidence to verify this prediction has been missing. Here, using an observation-based product of the oceanic partial pressure of CO2 (pCO2) covering the past 34 years, we find that the winter-to-summer difference of the pCO2 has increased on average by 2.2 ± 0.4 μatm per decade from 1982 to 2015 poleward of 10° latitude. This is largely in agreement with the trend expected from thermodynamic considerations. Most of the increase stems from the seasonality of the drivers acting on an increasing oceanic pCO2 caused by the uptake of anthropogenic CO2 from the atmosphere. In the high latitudes, the concurrent ocean-acidification-induced changes in the buffer capacity of the ocean enhance this effect. This strengthening of the seasonal winter-to-summer difference pushes the global ocean towards critical thresholds earlier, inducing stress to ocean ecosystems and fisheries4. Our study provides observational evidence for this strengthening seasonal difference in the oceanic carbon cycle on a global scale, illustrating the inevitable consequences of anthropogenic CO2 emissions.

  9. Atmospheric CO2 Variability Observed From ASCENDS Flight Campaigns

    NASA Technical Reports Server (NTRS)

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

    2015-01-01

    Significant atmospheric CO2 variations on various spatiotemporal scales were observed during ASCENDS flight campaigns. For example, around 10-ppm CO2 changes were found within free troposphere in a region of about 200x300 sq km over Iowa during a summer 2014 flight. Even over extended forests, about 2-ppm CO2 column variability was measured within about 500-km distance. For winter times, especially over snow covered ground, relatively less horizontal CO2 variability was observed, likely owing to minimal interactions between the atmosphere and land surface. Inter-annual variations of CO2 drawdown over cornfields in the Mid-West were found to be larger than 5 ppm due to slight differences in the corn growing phase and meteorological conditions even in the same time period of a year. Furthermore, considerable differences in atmospheric CO2 profiles were found during winter and summer campaigns. In the winter CO2 was found to decrease from about 400 ppm in the atmospheric boundary layer (ABL) to about 392 ppm above 10 km, while in the summer CO2 increased from 386 ppm in the ABL to about 396 ppm in free troposphere. These and other CO2 observations are discussed in this presentation.

  10. Aging behavior of near atmospheric N2 ambient sputtered/patterned Au IR absorber thin films

    NASA Astrophysics Data System (ADS)

    Gaur, Surender P.; Kothari, Prateek; Rangra, Kamaljit; Kumar, Dinesh

    2018-03-01

    Near atmospheric N2 ambient sputtered Au thin films exhibit significant spectral absorptivity over medium to long wave infrared radiations. Thin films were found adequately robust for micropatterning using conventional photolithography and metal lift off processes. Since long term spectral absorptivity is major practical concern for Au blacks, this paper reports on aging behavior of near atmospheric Ar and Ar + N2 (1:1) ambient sputtered infrared absorber Au thin films. Comparative analysis on electrical, morphological and spectral absorption behavior of twenty-five weeks room temperature/vacuum aged Au infrared absorber thin films is performed. The Ar and Ar + N2 ambient sputtered Au thing films have shown anticipated consistency in their physical, electrical and spectral properties regardless the long term aging in this work.

  11. Atmospheric measurement of point source fossil CO2 emissions

    NASA Astrophysics Data System (ADS)

    Turnbull, J. C.; Keller, E. D.; Baisden, T.; Brailsford, G.; Bromley, T.; Norris, M.; Zondervan, A.

    2014-05-01

    We use the Kapuni Gas Treatment Plant to examine methodologies for atmospheric monitoring of point source fossil fuel CO2 (CO2ff) emissions. The Kapuni plant, located in rural New Zealand, removes CO2 from locally extracted natural gas and vents that CO2 to the atmosphere, at a rate of ~0.1 Tg carbon per year. The plant is located in a rural dairy farming area, with no other significant CO2ff sources nearby, but large, diurnally varying, biospheric CO2 fluxes from the surrounding highly productive agricultural grassland. We made flask measurements of CO2 and 14CO2 (from which we derive the CO2ff component) and in situ measurements of CO2 downwind of the Kapuni plant, using a Helikite to sample transects across the emission plume from the surface up to 100 m above ground level. We also determined the surface CO2ff content averaged over several weeks from the 14C content of grass samples collected from the surrounding area. We use the WindTrax plume dispersion model to compare the atmospheric observations with the emissions reported by the Kapuni plant, and to determine how well atmospheric measurements can constrain the emissions. The model has difficulty accurately capturing the fluctuations and short-term variability in the Helikite samples, but does quite well in representing the observed CO2ff in 15 min averaged surface flask samples and in ~ one week integrated CO2ff averages from grass samples. In this pilot study, we found that using grass samples, the modeled and observed CO2ff emissions averaged over one week agreed to within 30%. The results imply that greater verification accuracy may be achieved by including more detailed meteorological observations and refining 14C sampling strategies.

  12. Atmospheric Collapse on Early Mars: The Role of CO2 Clouds

    NASA Technical Reports Server (NTRS)

    Kahre, M. A.; Haberle, R. M.; Steakley, K. E.; Murphy, J. R.; Kling, A.

    2017-01-01

    The abundance of evidence that liquid water flowed on the surface early in Mars' history strongly implies that the early Martian atmosphere was significantly more massive than it is today. While it seems clear that the total CO2 inventory was likely substantially larger in the past, the fundamental question about the physical state of that CO2 is not completely understood. Because the temperature at which CO2 condenses increases with surface pressure, surface CO2 ice is more likely to form and persist as the atmospheric mass increases. For the atmosphere to remain stable against collapse, there must be enough energy, distributed planet wide, to stave off the formation of permanent CO2 caps that leads to atmospheric collapse. The presence of a "faint young sun" that was likely about 25 percent less luminous 3.8 billion years ago than the sun today makes this even more difficult. Several physical processes play a role in the ultimate stability of a CO2 atmosphere. The system is regulated by the energy balance between solar insolation, the radiative effects of the atmosphere and its constituents, atmospheric heat transport, heat exchange between the surface and the atmosphere, and latent heating/cooling. Specific considerations in this balance for a given orbital obliquity/eccentricity and atmospheric mass are the albedo of the caps, the dust content of the atmosphere, and the presence of water and/or CO2 clouds. Forget et al. show that, for Mars' current obliquity (in a circular orbit), CO2 atmospheres ranging in surface pressure from 500 hectopascals to 3000 hectopascals would have been stable against collapsing into permanent surface ice reservoirs. Soto et al. examined a similar range in initial surface pressure to investigate atmospheric collapse and to compute collapse rates. CO2 clouds and their radiative effects were included in Forget et al. but they were not included in Soto et al. Here we focus on how CO2 clouds affect the stability of the atmosphere

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

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Levi, A.; Sasselov, D.; Podolak, M., E-mail: amitlevi.planetphys@gmail.com

    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 atmospheremore » 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.« less

  14. Impact of atmospheric CO2 levels on continental silicate weathering

    NASA Astrophysics Data System (ADS)

    Beaulieu, E.; GoddéRis, Y.; Labat, D.; Roelandt, C.; Oliva, P.; Guerrero, B.

    2010-07-01

    Anthropogenic sources are widely accepted as the dominant cause for the increase in atmospheric CO2 concentrations since the beginning of the industrial revolution. Here we use the B-WITCH model to quantify the impact of increased CO2 concentrations on CO2 consumption by weathering of continental surfaces. B-WITCH couples a dynamic biogeochemistry model (LPJ) and a process-based numerical model of continental weathering (WITCH). It allows simultaneous calculations of the different components of continental weathering fluxes, terrestrial vegetation dynamics, and carbon and water fluxes. The CO2 consumption rates are estimated at four different atmospheric CO2 concentrations, from 280 up to 1120 ppmv, for 22 sites characterized by silicate lithologies (basalt, granite, or sandstones). The sensitivity to atmospheric CO2 variations is explored, while temperature and rainfall are held constant. First, we show that under 355 ppmv of atmospheric CO2, B-WITCH is able to reproduce the global pattern of weathering rates as a function of annual runoff, mean annual temperature, or latitude for silicate lithologies. When atmospheric CO2 increases, evapotranspiration generally decreases due to progressive stomatal closure, and the soil CO2 pressure increases due to enhanced biospheric productivity. As a result, vertical drainage and soil acidity increase, promoting CO2 consumption by mineral weathering. We calculate an increase of about 3% of the CO2 consumption through silicate weathering (mol ha-1 yr-1) for 100 ppmv rise in CO2. Importantly, the sensitivity of the weathering system to the CO2 rise is not uniform and heavily depends on the climatic, lithologic, pedologic, and biospheric settings.

  15. Role of Atmospheric CO2 in the Ice Ages (Invited)

    NASA Astrophysics Data System (ADS)

    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.

  16. Regenerable Sorbent for CO2 Removal

    NASA Technical Reports Server (NTRS)

    Alptekin, Gokhan; Jayaraman, Ambal

    2013-01-01

    A durable, high-capacity regenerable sorbent can remove CO2 from the breathing loop under a Martian atmosphere. The system design allows near-ambient temperature operation, needs only a small temperature swing, and sorbent regeneration takes place at or above 8 torr, eliminating the potential for Martian atmosphere to leak into the regeneration bed and into the breathing loop. The physical adsorbent can be used in a metabolic, heat-driven TSA system to remove CO2 from the breathing loop of the astronaut and reject it to the Martian atmosphere. Two (or more) alternating sorbent beds continuously scrub and reject CO2 from the spacesuit ventilation loop. The sorbent beds are cycled, alternately absorbing CO2 from the vent loop and rejecting the adsorbed material into the environment at a high CO2 partial pressure (above 8 torr). The system does not need to run the adsorber at cryogenic temperatures, and uses a much smaller temperature swing. The sorbent removes CO2 via a weak chemical interaction. The interaction is strong enough to enable CO2 adsorption even at 3 to 7.6 torr. However, because the interaction between the surface adsorption sites and the CO2 is relatively weak, the heat input needed to regenerate the sorbent is much lower than that for chemical absorbents. The sorbent developed in this project could potentially find use in a large commercial market in the removal of CO2 emissions from coal-fired power plants, if regulations are put in place to curb carbon emissions from power plants.

  17. Lidar Measurements of Atmospheric CO2 From Regional to Global Scales

    NASA Technical Reports Server (NTRS)

    Lin, Bing; Harrison, F. Wallace; Nehrir, Amin; Browell, Edward; Dobler, Jeremy; Campbell, Joel; Meadows, Byron; Obland, Michael; Ismail, Syed; Kooi, Susan; hide

    2015-01-01

    Atmospheric CO2 is a critical forcing for the Earth's climate and the knowledge on its distributions and variations influences predictions of the Earth's future climate. Large uncertainties in the predictions persist due to limited observations. This study uses the airborne Intensity-Modulated Continuous-Wave (IMCW) lidar developed at NASA Langley Research Center to measure regional atmospheric CO2 spatio-temporal variations. Further lidar development and demonstration will provide the capability of global atmospheric CO2 estimations from space, which will significantly advances our knowledge on atmospheric CO2 and reduce the uncertainties in the predictions of future climate. In this presentation, atmospheric CO2 column measurements from airborne flight campaigns and lidar system simulations for space missions will be discussed. A measurement precision of approx.0.3 ppmv for a 10-s average over desert and vegetated surfaces has been achieved. Data analysis also shows that airborne lidar CO2 column measurements over these surfaces agree well with in-situ measurements. Even when thin cirrus clouds present, consistent CO2 column measurements between clear and thin cirrus cloudy skies are obtained. Airborne flight campaigns have demonstrated that precise atmospheric column CO2 values can be measured from current IM-CW lidar systems, which will lead to use this airborne technique in monitoring CO2 sinks and sources in regional and continental scales as proposed by the NASA Atmospheric Carbon and Transport â€" America project. Furthermore, analyses of space CO2 measurements shows that applying the current IM-CW lidar technology and approach to space, the CO2 science goals of space missions will be achieved, and uncertainties in CO2 distributions and variations will be reduced.

  18. Advanced EMU electrochemically regenerable CO2 and moisture absorber module breadboard

    NASA Technical Reports Server (NTRS)

    Lee, M. C.; Sudar, M.; Chang, B. J.

    1988-01-01

    The applicability of the Electrochemically Regenerable Carbon Dioxide and Moisture Absorption Technology to the advanced extravehicular mobility unit was demonstrated by designing, fabricating, and testing a breadboard Absorber Module and an Electrochemical Regenerator. Test results indicated that the absorber module meets or exceeds the carbon dioxide removal requirements specified for the design and can meet the moisture removal requirement when proper cooling is provided. CO2 concentration in the vent gas stream was reduced from 0.52 to 0.027 kPa (3.9 to 0.20 mm Hg) for the full five hour test period. Vent gas dew point was reduced from inlet values of 294 K (69 F) to 278 K (41 F) at the outlet. The regeneration of expended absorbent was achieved by the electrochemical method employed in the testing. An absorbent bed using microporous hydrophobic membrane sheets with circulating absorbent is shown to be the best approach to the design of an Absorber Module based on sizing and performance. Absorber Module safety design, comparison of various absorbents and their characteristics, moisture absorption and cooling study and subsystem design and operation time-lining study were also performed.

  19. Atmospheric verification of anthropogenic CO2 emission trends

    NASA Astrophysics Data System (ADS)

    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.

  20. A Southern Ocean driver of atmospheric CO2

    NASA Astrophysics Data System (ADS)

    Ronge, T.; Geibert, W.; Lippold, J.; Lamy, F.; Schnetger, B.; Tiedemann, R.

    2017-12-01

    A prominent two-step rise in atmospheric CO2 marked the end of the last glacial. The steps coincided with climatic intervals Heinrich Stadial 1 (HS1) and the Younger Dryas (YD). Records of 231Pa/230Th on sediment cores bathed by NADW, revealed a rapid reduction of the Atlantic Meridional Overturning Circulation (AMOC), during these intervals. It was argued that a weakened AMOC would have significantly reduced the efficiency of the biological pump and thus might have contributed to the rise in atmospheric CO2. Despite playing an important role, this process fails to account for the enigmatic drop in atmospheric Δ14C and δ13C during HS1 that marks the first step of the CO2-rise. Increasing CO2-concentrations with a simultaneous drop in their Δ14C, call for the ventilation of an old and 14C-depleted carbon reservoir. In this respect, several studies point to the presence of very old, 14C-depleted deep-waters in the glacial Southern Ocean, which rejuvenated during the last deglaciation. However, the accumulation of 14C-depleted, carbon-rich waters in the deep Southern Ocean requires circulation patterns that significantly differ from todays. Here we present a combined set of 231Pa/230Th-, Rare Earth Element- and XRF-proxy records to understand the evolution of the South Pacific Overturning Circulation (SPOC) over the last 35,000 years. Our reconstructions are based on a transect of five sediment cores from the Southwest Pacific, covering the AAIW as well as the UCDW and LCDW. Our data show that throughout the last glacial the SPOC was significantly weakened. This reduction favored the observed accumulation of 14C-depleted CO2 in Circumpolar Deep Waters (CDW). Parallel to the HS1 increase of atmospheric CO2, the deep circulation picked up its pace and recovered toward the Holocene. This trend is in remarkable agreement with water mass radiocarbon reconstructions from the very same area, as well as with atmospherical changes in CO2, Δ14C and δ13C. Hence, we are

  1. Positive feedback between increasing atmospheric CO2 and ecosystem productivity

    NASA Astrophysics Data System (ADS)

    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

  2. Prebiotic synthesis in atmospheres containing CH4, CO, and CO2. I - Amino acids

    NASA Technical Reports Server (NTRS)

    Schlesinger, G.; Miller, S. L.

    1983-01-01

    The prebiotic synthesis of amino acids, HCN, H2CO, and NH3 using a spark discharge on various simulated primitive earth atmospheres at 25 C is investigated. Various mixtures of CH4, CO, CO2, N2, NH3, H2O, and H2 were utilized in different experiments. The yields of amino acids (1.2-4.7 percent based on the carbon) are found to be approximately independent of the H2/CH4 ratio and the presence of NH3, and a wide variety of amino acids are obtained. Glycine is found to be almost the only amino acid produced from CO and CO2 model atmospheres, with the maximum yield being about the same for the three carbon sources at high H2/carbon ratios,whereas CH4 is superior at low H2/carbon ratios. In addition, it is found that the directly synthesized NH3 together with the NH3 obtained from the hydrolysis of HCN, nitriles, and urea could have been a major source of ammonia in the atmosphere and oceans of the primitive earth. It is determined that prebiotic syntheses from HCN and H2CO to give products such as purines and sugars and some amino acids could have occurred in primitive atmospheres containing CO and CO2 provided the H2/CO and H2/CO2 ratios were greater than about 1.0.

  3. Analysis of Urban Forest Needs as Anthropogenic (CO2) Gas Absorbent in Semarang City

    NASA Astrophysics Data System (ADS)

    Febriani, Anisa Putri; Retnaningsih Soeprobowati, Tri; Maryono

    2018-02-01

    Green open space in cities in significant needs to maintenance environment quality. On of the critical function is to absorb increasing number of gas CO2. Therefore, developing urban forest in cities is very importance. The objective of the study is to determine the area of urban forest as CO2 gas anthropogenic absorb which is formed from fuel, diesel fuel, liquid petroleum gas. The study consists of (1) Analyzing the number of CO2 gas emission by calculating the needs of petroleum and gas based on the number of population, (2) Analyzing the power of gas absorption, (3) Measuring the air concentration of CO2 gas ambient based on daily traffic activities. This study shown that from year 2013 to year 2017, the increasing of urban forest is not so significant. For year 2013 the green open space in Semarang City are 373.67 hectares (7.5 percent from Semarang City area), consists of 239 parks, 11 public cemeteries, production forests, community forests, and urban forests, however the area of urban forest is not increase. The study assess that Antidesmabunius is one of the green species which high absorb capacity planted for Semarang. This trees produce 31,31 ton annually. This study proposed to fostering Antidesmabunius as one principle threes in Semarang urban forest.

  4. Atmospheric measurement of point source fossil fuel CO2 emissions

    NASA Astrophysics Data System (ADS)

    Turnbull, J. C.; Keller, E. D.; Baisden, W. T.; Brailsford, G.; Bromley, T.; Norris, M.; Zondervan, A.

    2013-11-01

    We use the Kapuni Gas Treatment Plant to examine methodologies for atmospheric monitoring of point source fossil fuel CO2 (CO2ff) emissions. The Kapuni plant, located in rural New Zealand, removes CO2 from locally extracted natural gas and vents that CO2 to the atmosphere, at a rate of ~0.1 Tg carbon per year. The plant is located in a rural dairy farming area, with no other significant CO2ff sources nearby, but large, diurnally varying, biospheric CO2 fluxes from the surrounding highly productive agricultural grassland. We made flask measurements of CO2 and 14CO2 (from which we derive the CO2ff component) and in situ measurements of CO2 downwind of the Kapuni plant, using a Helikite to sample transects across the emission plume from the surface up to 100 m a.g.l. We also determined the surface CO2ff content averaged over several weeks from the 14CO2 content of grass samples collected from the surrounding area. We use the WindTrax plume dispersion model to compare the atmospheric observations with the emissions reported by the Kapuni plant, and to determine how well atmospheric measurements can constrain the emissions. The model has difficulty accurately capturing the fluctuations and short-term variability in the Helikite samples, but does quite well in representing the observed CO2ff in 15 min averaged surface flask samples and in ~1 week integrated CO2ff averages from grass samples. In this pilot study, we found that using grass samples, the modeled and observed CO2ff emissions averaged over one week agreed to within 30%. The results imply that greater verification accuracy may be achieved by including more detailed meteorological observations and refining 14CO2 sampling strategies.

  5. Atmospheric CO2: principal control knob governing Earth's temperature.

    PubMed

    Lacis, Andrew A; Schmidt, Gavin A; Rind, David; Ruedy, Reto A

    2010-10-15

    Ample physical evidence shows that carbon dioxide (CO(2)) is the single most important climate-relevant greenhouse gas in Earth's atmosphere. This is because CO(2), like ozone, N(2)O, CH(4), and chlorofluorocarbons, does not condense and precipitate from the atmosphere at current climate temperatures, whereas water vapor can and does. Noncondensing greenhouse gases, which account for 25% of the total terrestrial greenhouse effect, thus serve to provide the stable temperature structure that sustains the current levels of atmospheric water vapor and clouds via feedback processes that account for the remaining 75% of the greenhouse effect. Without the radiative forcing supplied by CO(2) and the other noncondensing greenhouse gases, the terrestrial greenhouse would collapse, plunging the global climate into an icebound Earth state.

  6. Commander Lousma stows trash bags in middeck CO2 Absorber Stowage volume

    NASA Technical Reports Server (NTRS)

    1982-01-01

    Commander Lousma uses his body as a zero gravity garbage compactor to stow plastic bags full of empty containers and trash in the Carbon Dioxide (CO2) Absorber Stowage volume in front of the airlock hatch.

  7. The Impact of Atmospheric Aerosols on the Fraction of absorbed Photosynthetically Active Radiation

    NASA Astrophysics Data System (ADS)

    Veroustraete, Frank

    2010-05-01

    Aerosol pollution attracts a growing interest from atmospheric scientists with regard to their impact on health, the global climate and vegetation stress. A hypothesis, less investigated, is whether atmospheric aerosol interactions in the solar radiation field affect the amount of radiation absorbed by vegetation canopies and hence terrestrial vegetation productivity. Typically, aerosols affect vegetation canopy radiation absorption efficiency by altering the physical characteristics of solar radiation incoming on for example a forest canopy. It has been illustrated, that increasing mixing ratio's of atmospheric particulate matter lead to a higher fraction of diffuse sunlight as opposed to direct sunlight. It can be demonstrated, based on the application of atmospheric (MODTRAN) and leaf/canopy radiative transfer (LIBERTY/SPRINT) models, that radiation absorption efficiency in the PAR band of Picea like forests increases with increasing levels of diffuse radiation. It can be documented - on a theoretical basis - as well, that increasing aerosol loads in the atmosphere, induce and increased canopy PAR absorption efficiency. In this paper it is suggested, that atmospheric aerosols have to be taken into account when estimating vegetation gross primary productivity (GPP). The results suggest that Northern hemisphere vegetation CO2 uptake magnitude may increase with increasing atmospheric aerosol loads. Many climate impact scenario's related to vegetation productivity estimates, do not take this phenomenon into account. Boldly speaking, the results suggest a larger sink function for terrestrial vegetation than generally accepted. Keywords: Aerosols, vegetation, fAPAR, CO2 uptake, diffuse radiation.

  8. Physiological Significance of Low Atmospheric CO 2 for Plant-Climate Interactions

    NASA Astrophysics Data System (ADS)

    Cowling, Sharon A.; Sykes, Martin T.

    1999-09-01

    Methods of palaeoclimate reconstruction from pollen are built upon the assumption that plant-climate interactions remain the same through time or that these interactions are independent of changes in atmospheric CO2. The latter may be problematic because air trapped in polar ice caps indicates that atmospheric CO2 has fluctuated significantly over at least the past 400,000 yr, and likely the last 1.6 million yr. Three other points indicate potential biases for vegetation-based climate proxies. First, C3-plant physiological research shows that the processes that determine growth optima in plants (photosynthesis, mitochondrial respiration, photorespiration) are all highly CO2-dependent, and thus were likely affected by the lower CO2 levels of the last glacial maximum. Second, the ratio of carbon assimilation per unit transpiration (called water-use efficiency) is sensitive to changes in atmospheric CO2 through effects on stomatal conductance and may have altered C3-plant responses to drought. Third, leaf gas-exchange experiments indicate that the response of plants to carbon-depleting environmental stresses are strengthened under low CO2 relative to today. This paper reviews the scope of research addressing the consequences of low atmospheric CO2 for plant and ecosystem processes and highlights why consideration of the physiological effects of low atmospheric CO2 on plant function is recommended for any future refinements to pollen-based palaeoclimatic reconstructions.

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

    Treesearch

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

    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...

  10. [Simulation of CO2 exchange between forest canopy and atmosphere].

    PubMed

    Diao, Yiwei; Wang, Anzhi; Jin, Changjie; Guan, Dexin; Pei, Tiefan

    2006-12-01

    Estimating the scalar source/sink distribution of CO2 and its vertical fluxes within and above forest canopy continues to be a critical research problem in biosphere-atmosphere exchange processes and plant ecology. With broad-leaved Korean pine forest in Changbai Mountains as test object, and based on Raupach's localized near field theory, the source/sink and vertical flux distribution of CO2 within and above forest canopy were modeled through an inverse Lagrangian dispersion analysis. This model correctly predicted a strong positive CO2 source strength in the deeper layers of the canopy due to soil-plant respiration, and a strong CO2 sink in the upper layers of the canopy due to the assimilation by sunlit foliage. The foliage in the top layer of canopy changed from a CO2 source in the morning to a CO2 sink in the afternoon, while the soil constituted a strong CO2 source all the day. The simulation results accorded well with the eddy covariance CO2 flux measurements within and above the canopy, and the average precision was 89%. The CO2 exchange predicted by the analysis was averagely 15% higher than that of the eddy correlation, but exhibited identical temporal trend. Atmospheric stability remarkably affected the CO2 exchange between forest canopy and atmosphere.

  11. Postglacial Terrestrial Carbon Dynamics and Atmospheric CO2

    NASA Astrophysics Data System (ADS)

    Prentice, C. I.; Harrison, S. P.; Kaplan, J. O.

    2002-12-01

    Combining PMIP climate model results from the last glacial maximum (LGM) with biome modelling indicates the involvement of both cold, dry climate and physiological effects of low atmospheric CO2 in reducing tree cover on the continents. Further results with the LPJ dynamic vegetation model agree with independent evidence for greatly reduced terrestrial carbon storage at LGM, and suggest that terrestrial carbon storage continued to increase during the Holocene. These results point to predominantly oceanic explanations for preindustrial changes in atmospheric CO2, although land changes after the LGM may have contributed indirectly by reducing the aeolian marine Fe source and (on a longer time scale) by triggering CaCO3 compensation in the ocean.

  12. [Quantitative estimation source of urban atmospheric CO2 by carbon isotope composition].

    PubMed

    Liu, Wei; Wei, Nan-Nan; Wang, Guang-Hua; Yao, Jian; Zeng, You-Shi; Fan, Xue-Bo; Geng, Yan-Hong; Li, Yan

    2012-04-01

    To effectively reduce urban carbon emissions and verify the effectiveness of currently project for urban carbon emission reduction, quantitative estimation sources of urban atmospheric CO2 correctly is necessary. Since little fractionation of carbon isotope exists in the transportation from pollution sources to the receptor, the carbon isotope composition can be used for source apportionment. In the present study, a method was established to quantitatively estimate the source of urban atmospheric CO2 by the carbon isotope composition. Both diurnal and height variations of concentrations of CO2 derived from biomass, vehicle exhaust and coal burning were further determined for atmospheric CO2 in Jiading district of Shanghai. Biomass-derived CO2 accounts for the largest portion of atmospheric CO2. The concentrations of CO2 derived from the coal burning are larger in the night-time (00:00, 04:00 and 20:00) than in the daytime (08:00, 12:00 and 16:00), and increase with the increase of height. Those derived from the vehicle exhaust decrease with the height increase. The diurnal and height variations of sources reflect the emission and transport characteristics of atmospheric CO2 in Jiading district of Shanghai.

  13. Net uptake of atmospheric CO2 by coastal submerged aquatic vegetation

    PubMed Central

    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

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

    NASA Astrophysics Data System (ADS)

    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

  15. Detection of CO2 leaks from carbon capture and storage sites to the atmosphere with combined CO2 and O2 measurements

    NASA Astrophysics Data System (ADS)

    van Leeuwen, Charlotte; Meijer, Harro A. J.

    2015-04-01

    One of the main issues in carbon capture and storage (CCS) is the possibility of leakage of CO2 from the storage reservoir to the atmosphere, both from a public health and a climate change combat perspective. Detecting these leaks in the atmosphere is difficult due to the rapid mixing of the emitted CO2 with the surrounding air masses and the high natural variability of the atmospheric CO2 concentration. Instead of measuring only the CO2 concentration of the atmosphere, its isotopes or chemical tracers that are released together with the CO2, our method uses O2 measurements in addition to CO2 measurements to detect a leak from a CCS site. CO2 and O2 are coupled in most processes on earth. In photosynthesis, plants take up CO2 and release O2 at the same time. In respiration and fossil fuel burning, O2 is consumed while CO2 is released. In case of a leak from a CCS site, however, there is no relationship between CO2 and O2. A CO2 leak can therefore be distinguished from other sources of CO2 by looking at the atmospheric CO2-O2 ratio. A natural increase of the CO2 concentration is accompanied by a drop in the O2 concentration, while an increase in the CO2 concentration caused by a leak from a CCS site does not have any effect on the O2 concentration. To demonstrate this leak detection strategy we designed and built a transportable CO2 and O2 measurement system, that is capable of measuring the relatively minute (ppm's variations on a 21% concentration) changes in the O2 concentration. The system comprises of three cases that contain the instrumentation and gas handling equipment, the gas cylinders used as reference and calibration gases and a drying system, respectively. Air is pumped to the system from an air inlet that is placed in a small tower in the field. At the conference, we will demonstrate the success of leak detection with our system by showing measurements of several CO2 release experiments, where CO2 was released at a small distance from the air inlet of

  16. Atmospheric CO2 capture by algae: Negative carbon dioxide emission path.

    PubMed

    Moreira, Diana; Pires, José C M

    2016-09-01

    Carbon dioxide is one of the most important greenhouse gas, which concentration increase in the atmosphere is associated to climate change and global warming. Besides CO2 capture in large emission point sources, the capture of this pollutant from atmosphere may be required due to significant contribution of diffuse sources. The technologies that remove CO2 from atmosphere (creating a negative balance of CO2) are called negative emission technologies. Bioenergy with Carbon Capture and Storage may play an important role for CO2 mitigation. It represents the combination of bioenergy production and carbon capture and storage, keeping carbon dioxide in geological reservoirs. Algae have a high potential as the source of biomass, as they present high photosynthetic efficiencies and high biomass yields. Their biomass has a wide range of applications, which can improve the economic viability of the process. Thus, this paper aims to assess the atmospheric CO2 capture by algal cultures. Copyright © 2016 Elsevier Ltd. All rights reserved.

  17. Contributions to accelerating atmospheric CO2 growth from economic activity, carbon intensity, and efficiency of natural sinks.

    PubMed

    Canadell, Josep G; Le Quéré, Corinne; Raupach, Michael R; Field, Christopher B; Buitenhuis, Erik T; Ciais, Philippe; Conway, Thomas J; Gillett, Nathan P; Houghton, R A; Marland, Gregg

    2007-11-20

    The growth rate of atmospheric carbon dioxide (CO(2)), the largest human contributor to human-induced climate change, is increasing rapidly. Three processes contribute to this rapid increase. Two of these processes concern emissions. Recent growth of the world economy combined with an increase in its carbon intensity have led to rapid growth in fossil fuel CO(2) emissions since 2000: comparing the 1990s with 2000-2006, the emissions growth rate increased from 1.3% to 3.3% y(-1). The third process is indicated by increasing evidence (P = 0.89) for a long-term (50-year) increase in the airborne fraction (AF) of CO(2) emissions, implying a decline in the efficiency of CO(2) sinks on land and oceans in absorbing anthropogenic emissions. Since 2000, the contributions of these three factors to the increase in the atmospheric CO(2) growth rate have been approximately 65 +/- 16% from increasing global economic activity, 17 +/- 6% from the increasing carbon intensity of the global economy, and 18 +/- 15% from the increase in AF. An increasing AF is consistent with results of climate-carbon cycle models, but the magnitude of the observed signal appears larger than that estimated by models. All of these changes characterize a carbon cycle that is generating stronger-than-expected and sooner-than-expected climate forcing.

  18. Contributions to accelerating atmospheric CO2 growth from economic activity, carbon intensity, and efficiency of natural sinks

    PubMed Central

    Canadell, Josep G.; Le Quéré, Corinne; Raupach, Michael R.; Field, Christopher B.; Buitenhuis, Erik T.; Ciais, Philippe; Conway, Thomas J.; Gillett, Nathan P.; Houghton, R. A.; Marland, Gregg

    2007-01-01

    The growth rate of atmospheric carbon dioxide (CO2), the largest human contributor to human-induced climate change, is increasing rapidly. Three processes contribute to this rapid increase. Two of these processes concern emissions. Recent growth of the world economy combined with an increase in its carbon intensity have led to rapid growth in fossil fuel CO2 emissions since 2000: comparing the 1990s with 2000–2006, the emissions growth rate increased from 1.3% to 3.3% y−1. The third process is indicated by increasing evidence (P = 0.89) for a long-term (50-year) increase in the airborne fraction (AF) of CO2 emissions, implying a decline in the efficiency of CO2 sinks on land and oceans in absorbing anthropogenic emissions. Since 2000, the contributions of these three factors to the increase in the atmospheric CO2 growth rate have been ≈65 ± 16% from increasing global economic activity, 17 ± 6% from the increasing carbon intensity of the global economy, and 18 ± 15% from the increase in AF. An increasing AF is consistent with results of climate–carbon cycle models, but the magnitude of the observed signal appears larger than that estimated by models. All of these changes characterize a carbon cycle that is generating stronger-than-expected and sooner-than-expected climate forcing. PMID:17962418

  19. Using radiocarbon to investigate soil respiration impacts on atmospheric CO2

    NASA Astrophysics Data System (ADS)

    Phillips, C. L.; LaFranchi, B. W.; McFarlane, K. J.; Desai, A. R.

    2013-12-01

    While soil respiration is believed to represent the largest single source of CO2 emissions on a global scale, there are few tools available to measure soil emissions at large spatial scales. We investigated whether radiocarbon (14C) abundance in CO2 could be used to detect and characterize soil emissions in the atmosphere, taking advantage of the fact that 14C abundance in soil carbon is elevated compared to the background atmosphere, a result of thermonuclear weapons testing during the mid-20th Century (i.e. bomb-C). Working in a temperate hardwood forest in Northern Wisconsin during 2011-12, we made semi-high-frequency measurements of CO2 at nested spatial scales from the soil subsurface to 150 m above ground level. These measurements were used to investigate seasonal patterns in respired C sources, and to evaluate whether variability in soil-respired Δ14C could also be detected in atmospheric measurements. In our ground-level measurements we found large seasonal variation in soil-respired 14CO2 that correlated with soil moisture, which was likely related to root activity. Atmospheric measurements of 14CO2 in the forest canopy (2 to 30m) were used to construct Keeling plots, and these provided larger spatial-scale estimates of respired 14CO2 that largely agreed with the soil-level measurements. In collaboration with the NOAA we also examined temporal patterns of 14CO2 at the Park Falls tall-tower (150m), and found elevated 14CO2 levels during summer months that likely resulted from increased respiration from heterotrophic sources. These results demonstrate that a fingerprint from soil-respired CO2 can be detected in the seasonal patterns of atmospheric 14CO2, even at a regionally-integrating spatial scale far from the soil surface.

  20. Atmospheric CO2 and abrupt climate change on submillennial timescales

    NASA Astrophysics Data System (ADS)

    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

  1. Atmospheric Backscatter Model Development for CO Sub 2 Wavelengths

    NASA Technical Reports Server (NTRS)

    Deepak, A.; Kent, G.; Yue, G. K.

    1982-01-01

    The results of investigations into the problems of modeling atmospheric backscatter from aerosols, in the lowest 20 km of the atmosphere, at CO2 wavelengths are presented, along with a summary of the relevant aerosol characteristics and their variability, and a discussion of the measurement techniques and errors involved. The different methods of calculating the aerosol backscattering function, both from measured aerosol characteristics and from optical measurements made at other wavelengths, are discussed in detail, and limits are placed on the accuracy of these methods. The effects of changing atmospheric humidity and temperature on the backscatter are analyzed and related to the actual atmosphere. Finally, the results of modeling CO2 backscatter in the atmosphere are presented and the variation with height and geographic location discussed, and limits placed on the magnitude of the backscattering function. Conclusions regarding modeling techniques and modeled atmospheric backscatter values are presented in tabular form.

  2. Simulated effect of calcification feedback on atmospheric CO2 and ocean acidification

    PubMed Central

    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

  3. STABILITY OF CO{sub 2} ATMOSPHERES ON DESICCATED M DWARF EXOPLANETS

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Gao, Peter; Hu, Renyu; Li, Cheng

    2015-06-20

    We investigate the chemical stability of CO{sub 2}-dominated atmospheres of desiccated M dwarf terrestrial exoplanets using a one-dimensional photochemical model. Around Sun-like stars, CO{sub 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{sub 2}O{sub 2} photolysis can maintain a CO{sub 2} atmosphere. However, this cycle breaks down for atmospheric hydrogen mixing ratios <1 ppm, resultingmore » in ∼40% of the atmospheric CO{sub 2} being converted to CO and O{sub 2} on a timescale of 1 Myr. The increased O{sub 2} abundance leads to high O{sub 3} concentrations, the photolysis of which forms another CO{sub 2}-regenerating catalytic cycle. For atmospheres with <0.1 ppm hydrogen, CO{sub 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{sub 2} that can be destroyed via photolysis, which is enough to generate Earth-like abundances of (abiotic) O{sub 2} and O{sub 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{sub 2} and O{sub 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.« less

  4. 2-Micron Pulsed Direct Detection IPDA Lidar for Atmospheric CO2 Measurement

    NASA Technical Reports Server (NTRS)

    Yu, Jirong; Petros, Mulugeta; Refaat, Tamer; Reithmaier, Karl; Remus, Ruben; Singh, Upendra; Johnson, Will; Boyer, Charlie; Fay, James; Johnston, Susan; hide

    2014-01-01

    A 2-micron high energy, pulsed Integrated Path Differential Absorption (IPDA) lidar has been developed for atmospheric CO2 measurements. Development of this lidar heavily leverages the 2-micron laser technologies developed in LaRC over the last decade. The high pulse energy, direct detection lidar operating at CO2 2-micron absorption band provides an alternate approach to measure CO2 concentrations. This new 2-micron pulsed IPDA lidar has been flown in spring of this year for total ten flights with 27 flight hours. It is able to make measurements of the total amount of atmospheric CO2 from the aircraft to the ground or cloud. It is expected to provide high-precision measurement capability by unambiguously eliminating contamination from aerosols and clouds that can bias the IPDA measurement.

  5. A process for capturing CO 2 from the atmosphere

    DOE PAGES

    Keith, David W.; Holmes, Geoffrey; St. Angelo, David; ...

    2018-06-07

    Here, we describe a process for capturing CO 2 from the atmosphere in an industrial plant. The design captures ~1 Mt-CO 2/year in a continuous process using an aqueous KOH sorbent coupled to a calcium caustic recovery loop. We describe the design rationale, summarize performance of the major unit operations, and provide a capital cost breakdown developed with an independent consulting engineering firm. We report results from a pilot plant which provides data on performance of the major unit operations. We summarize the energy and material balance computed using an Aspen process simulation. When CO 2 is delivered at 15more » MPa the design requires either 8.81 GJ of natural gas, or 5.25 GJ of gas and 366 kWhr of electricity, per ton of CO 2 captured. Depending on financial assumptions, energy costs, and the specific choice of inputs and outputs, the levelized cost per ton CO 2 captured from the atmosphere ranges from 94 to 232 $/t-CO 2.« less

  6. A process for capturing CO 2 from the atmosphere

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Keith, David W.; Holmes, Geoffrey; St. Angelo, David

    Here, we describe a process for capturing CO 2 from the atmosphere in an industrial plant. The design captures ~1 Mt-CO 2/year in a continuous process using an aqueous KOH sorbent coupled to a calcium caustic recovery loop. We describe the design rationale, summarize performance of the major unit operations, and provide a capital cost breakdown developed with an independent consulting engineering firm. We report results from a pilot plant which provides data on performance of the major unit operations. We summarize the energy and material balance computed using an Aspen process simulation. When CO 2 is delivered at 15more » MPa the design requires either 8.81 GJ of natural gas, or 5.25 GJ of gas and 366 kWhr of electricity, per ton of CO 2 captured. Depending on financial assumptions, energy costs, and the specific choice of inputs and outputs, the levelized cost per ton CO 2 captured from the atmosphere ranges from 94 to 232 $/t-CO 2.« less

  7. Rapid Removal of Atmospheric CO2 by Urban Soils.

    PubMed

    Washbourne, Carla-Leanne; Lopez-Capel, Elisa; Renforth, Phil; Ascough, Philippa L; Manning, David A C

    2015-05-05

    The measured calcium carbonate content of soils to a depth of 100 mm at a large urban development site has increased over 18 months at a rate that corresponds to the sequestration of 85 t of CO2/ha (8.5 kg of CO2 m(-2)) annually. This is a consequence of rapid weathering of calcium silicate and hydroxide minerals derived from the demolition of concrete structures, which releases Ca that combines with CO2 ultimately derived from the atmosphere, precipitating as calcite. Stable isotope data confirm an atmospheric origin for carbonate carbon, and 14C dating indicates the predominance of modern carbon in the pedogenic calcite. Trial pits show that carbonation extends to depths of ≥1 m. Work at other sites shows that the occurrence of pedogenic carbonates is widespread in artificially created urban soils containing Ca and Mg silicate minerals. Appropriate management of fewer than 12000 ha of urban land to maximize calcite precipitation has the potential to remove 1 million t of CO2 from the atmosphere annually. The maximal global potential is estimated to be approximately 700-1200 Mt of CO2 per year (representing 2.0-3.7% of total emissions from fossil fuel combustion) based on current rates of production of industry-derived Ca- and Mg-bearing materials.

  8. Spatial response of coastal marshes to increased atmospheric CO2.

    PubMed

    Ratliff, Katherine M; Braswell, Anna E; Marani, Marco

    2015-12-22

    The elevation and extent of coastal marshes are dictated by the interplay between the rate of relative sea-level rise (RRSLR), surface accretion by inorganic sediment deposition, and organic soil production by plants. These accretion processes respond to changes in local and global forcings, such as sediment delivery to the coast, nutrient concentrations, and atmospheric CO2, but their relative importance for marsh resilience to increasing RRSLR remains unclear. In particular, marshes up-take atmospheric CO2 at high rates, thereby playing a major role in the global carbon cycle, but the morphologic expression of increasing atmospheric CO2 concentration, an imminent aspect of climate change, has not yet been isolated and quantified. Using the available observational literature and a spatially explicit ecomorphodynamic model, we explore marsh responses to increased atmospheric CO2, relative to changes in inorganic sediment availability and elevated nitrogen levels. We find that marsh vegetation response to foreseen elevated atmospheric CO2 is similar in magnitude to the response induced by a varying inorganic sediment concentration, and that it increases the threshold RRSLR initiating marsh submergence by up to 60% in the range of forcings explored. Furthermore, we find that marsh responses are inherently spatially dependent, and cannot be adequately captured through 0-dimensional representations of marsh dynamics. Our results imply that coastal marshes, and the major carbon sink they represent, are significantly more resilient to foreseen climatic changes than previously thought.

  9. Role of Southern Ocean stratification in glacial atmospheric CO2 reduction

    NASA Astrophysics Data System (ADS)

    Kobayashi, H.; Oka, A.

    2014-12-01

    Paleoclimate proxy data at the glacial period shows high salinity of more than 37.0 psu in the deep South Atlantic. At the same time, data also indicate that the residence time of the water mass was more than 3000 years. These data implies that the stratification by salinity was stronger in the deep Southern Ocean (SO) in the Last Glacial Maximum (LGM). Previous studies using Ocean General Circulation Model (OGCM) fail to explain the low glacial atmospheric carbon dioxide (CO2) concentration at LGM. The reproducibility of salinity and water mass age is considered insufficient in these OGCMs, which may in turn affect the reproducibility of the atmospheric CO2concentration. In coarse-resolution OGCMs, The deep water is formed by unrealistic open-ocean deep convection in the SO. Considering these facts, we guessed previous studies using OGCM underestimated the salinity and water mass age at LGM. This study investigate the role of the enhanced stratification in the glacial SO on the variation of atmospheric CO2 concentration by using OGCM. In order to reproduce the recorded salinity of the deep water, relaxation of salinity toward value of recorded data is introduced in our OGCM simulations. It was found that deep water formation in East Antarctica is required for explaining the high salinity in the South Atlantic. In contrast, it is difficult to explain the glacial water mass age, even if we assume the situation vertical mixing is very weak in the SO. Contrary to previous estimate, the high salinity of the deep SO resulted in increase of Antarctic Bottom water (AABW) flow and decrease the residence time of carbon in the deep ocean, which increased atmospheric CO2 concentration. On the other hand, the weakening of the vertical mixing in the SO contributed to increase the vertical gradient of dissolved inorganic carbon (DIC), which decreased atmospheric CO2 concentration. Adding the contribution of the enhanced stratification in the glacial SO, we obtained larger

  10. Airborne Double Pulsed 2-Micron IPDA Lidar for Atmospheric CO2 Measurement

    NASA Technical Reports Server (NTRS)

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

    2015-01-01

    We have developed an airborne 2-micron Integrated Path Differential Absorption (IPDA) lidar for atmospheric CO2 measurements. The double pulsed, high pulse energy lidar instrument can provide high-precision CO2 column density measurements.

  11. Modeling Atmospheric CO2 Processes to Constrain the Missing Sink

    NASA Technical Reports Server (NTRS)

    Kawa, S. R.; Denning, A. S.; Erickson, D. J.; Collatz, J. C.; Pawson, S.

    2005-01-01

    We report on a NASA supported modeling effort to reduce uncertainty in carbon cycle processes that create the so-called missing sink of atmospheric CO2. Our overall objective is to improve characterization of CO2 source/sink processes globally with improved formulations for atmospheric transport, terrestrial uptake and release, biomass and fossil fuel burning, and observational data analysis. The motivation for this study follows from the perspective that progress in determining CO2 sources and sinks beyond the current state of the art will rely on utilization of more extensive and intensive CO2 and related observations including those from satellite remote sensing. The major components of this effort are: 1) Continued development of the chemistry and transport model using analyzed meteorological fields from the Goddard Global Modeling and Assimilation Office, with comparison to real time data in both forward and inverse modes; 2) An advanced biosphere model, constrained by remote sensing data, coupled to the global transport model to produce distributions of CO2 fluxes and concentrations that are consistent with actual meteorological variability; 3) Improved remote sensing estimates for biomass burning emission fluxes to better characterize interannual variability in the atmospheric CO2 budget and to better constrain the land use change source; 4) Evaluating the impact of temporally resolved fossil fuel emission distributions on atmospheric CO2 gradients and variability. 5) Testing the impact of existing and planned remote sensing data sources (e.g., AIRS, MODIS, OCO) on inference of CO2 sources and sinks, and use the model to help establish measurement requirements for future remote sensing instruments. The results will help to prepare for the use of OCO and other satellite data in a multi-disciplinary carbon data assimilation system for analysis and prediction of carbon cycle changes and carbodclimate interactions.

  12. The Effect of CO2 Ice Cap Sublimation on Mars Atmosphere

    NASA Technical Reports Server (NTRS)

    Batterson, Courtney

    2016-01-01

    Sublimation of the polar CO2 ice caps on Mars is an ongoing phenomenon that may be contributing to secular climate change on Mars. The transfer of CO2 between the surface and atmosphere via sublimation and deposition may alter atmospheric mass such that net atmospheric mass is increasing despite seasonal variations in CO2 transfer. My study builds on previous studies by Kahre and Haberle that analyze and compare data from the Phoenix and Viking Landers 1 and 2 to determine whether secular climate change is happening on Mars. In this project, I use two years worth of temperature, pressure, and elevation data from the MSL Curiosity rover to create a program that allows for successful comparison of Curiosity pressure data to Viking Lander pressure data so a conclusion can be drawn regarding whether CO2 ice cap sublimation is causing a net increase in atmospheric mass and is thus contributing to secular climate change on Mars.

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

    PubMed

    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.

  14. Development of a mobile and high-precision atmospheric CO2 monitoring station

    NASA Astrophysics Data System (ADS)

    Molnár, M.; Haszpra, L.; Major, I.; Svingor, É.; Veres, M.

    2009-04-01

    Nowadays one of the most burning questions for the science is the rate and the reasons of the recent climate change. Greenhouse gases (GHG), mainly CO2 and CH4 in the atmosphere could affect the climate of our planet. However, the relation between the amount of atmospheric GHG and the climate is complex, full with interactions and feedbacks partly poorly known even by now. The only way to understand the processes, to trace the changes, to develop and validate mathematical models for forecasts is the extensive, high precision, continuous monitoring of the atmosphere. Fossil fuel CO2 emissions are a major component of the European carbon budget. Separation of the fossil fuel signal from the natural biogenic one in the atmosphere is, therefore, a crucial task for quantifying exchange flux of the continental biosphere through atmospheric observations and inverse modelling. An independent method to estimate trace gas emissions is the top-down approach, using atmospheric CO2 concentration measurements combined with simultaneous radiocarbon (14C) observations. As adding fossil fuel CO2 to the atmosphere, therefore, leads not only to an increase in the CO2 content of the atmosphere but also to a decrease in the 14C/12C ratio in atmospheric CO2. The ATOMKI has more than two decade long experience in atmospheric 14CO2 monitoring. As a part of an ongoing research project being carried out in Hungary to investigate the amount and temporal and spatial variations of fossil fuel CO2 in the near surface atmosphere we developed a mobile and high-precision atmospheric CO2 monitoring station. We describe the layout and the operation of the measuring system which is designed for the continuous, unattended monitoring of CO2 mixing ratio in the near surface atmosphere based on an Ultramat 6F (Siemens) infrared gas analyser. In the station one atmospheric 14CO2 sampling unit is also installed which is developed and widely used since more than one decade by ATOMKI. Mixing ratio of CO2 is

  15. Climate change and the middle atmosphere. I - The doubled CO2 climate

    NASA Technical Reports Server (NTRS)

    Rind, D.; Prather, M. J.; Suozzo, R.; Balachandran, N. K.

    1990-01-01

    The effect of doubling the atmospheric content of CO2 on the middle-atmosphere climate is investigated using the GISS global climate model. In the standard experiment, the CO2 concentration is doubled both in the stratosphere and troposphere, and the SSTs are increased to match those of the doubled CO2 run of the GISS model. Results show that the doubling of CO2 leads to higher temperatures in the troposphere, and lower temperatures in the stratosphere, with a net result being a decrease of static stability for the atmosphere as a whole. The middle atmosphere dynamical differences found were on the order of 10-20 percent of the model values for the current climate. These differences, along with the calculated temperature differences of up to about 10 C, may have a significant impact on the chemistry of the future atmosphere, including that of stratospheric ozone, the polar ozone 'hole', and basic atmospheric composition.

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

    NASA Technical Reports Server (NTRS)

    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.

  17. Assessing Atmospheric CO2 Entrapped in Clay Nanotubes using Residual Gas Analyzer.

    PubMed

    Das, Sankar; Maity, Abhijit; Pradhan, Manik; Jana, Subhra

    2016-02-16

    A residual gas analyzer (RGA) coupled with a high-vacuum chamber has been explored to measure atmospheric CO2 entrapped in aminosilane-modified clay nanotubes. Ambient CO2 uptake efficacy together with stability of these novel adsorbents composed of both primary and/or secondary amine sites has been demonstrated at standard ambient temperature and pressure. The unprecedented sensitivity and accuracy of the RGA-based mass spectrometry technique toward atmospheric CO2 measurement has been substantiated with a laser-based optical cavity-enhanced integrated cavity output spectroscopy. The adsorption kinetics of atmospheric CO2 on amine-functionalized clay nanotubes followed the fractional-order kinetic model compared to that of the pseudo-first-order or pseudo-second-order rate equations. The efficiency along with stability of these novel adsorbents has also been demonstrated by their repetitive use for CO2 capture in the oxidative environment. Our findings thus point to a fundamental study on the atmospheric CO2 adsorption by amine-loaded adsorbents using an easy handling and low-cost benchtop RGA-based mass spectrometer, opening a new strategy for CO2 capture and sequestering study.

  18. Modeling the transformation of atmospheric CO2 into microalgal biomass.

    PubMed

    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

  19. Climatic implications of the simultaneous presence of CO2 and H2O in the Martian regolith

    NASA Technical Reports Server (NTRS)

    Zent, A. P.

    1992-01-01

    The current paradigm for quasi-periodic climate change on Mars holds that perhaps a few hundred millibars of CO2 are available for exchange between the atmosphere and regolith, and that a vast majority of that CO2 is presently absorbed into the regolith. The CO2 is partitioned between the regolith and atmosphere according to an equilibrium adsorptive relationship. If the atmospheric pressure exceeds the frost point at or near the poles, then quasi-permanent polar caps form and buffer the atmospheric pressure. This model was developed based upon laboratory studies of CO2 adsorption where no other adsorbates are present. We will conduct laboratory measurements of the simultaneous adsorption of H2O and CO2 under Mars-like conditions, and develop numerical expressions for use in climate modeling based upon our results.

  20. Bench Scale Process for Low Cost CO 2 Capture Using a Phase-Changing Absorbent: Final Scientific/Technical Report

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Westendorf, Tiffany; Buddle, Stanlee; Caraher, Joel

    The objective of this project is to design and build a bench-scale process for a novel phase-changing aminosilicone-based CO 2-capture solvent. The project will establish scalability and technical and economic feasibility of using a phase-changing CO 2-capture absorbent for post-combustion capture of CO 2 from coal-fired power plants. The U.S. Department of Energy’s goal for Transformational Carbon Capture Technologies is the development of technologies available for demonstration by 2025 that can capture 90% of emitted CO 2 with at least 95% CO 2 purity for less than $40/tonne of CO 2 captured. In the first budget period of the project,more » the bench-scale phase-changing CO2 capture process was designed using data and operating experience generated under a previous project (ARPA-e project DE-AR0000084). Sizing and specification of all major unit operations was completed, including detailed process and instrumentation diagrams. The system was designed to operate over a wide range of operating conditions to allow for exploration of the effect of process variables on CO 2 capture performance. In the second budget period of the project, individual bench-scale unit operations were tested to determine the performance of each of each unit. Solids production was demonstrated in dry simulated flue gas across a wide range of absorber operating conditions, with single stage CO 2 conversion rates up to 75mol%. Desorber operation was demonstrated in batch mode, resulting in desorption performance consistent with the equilibrium isotherms for GAP-0/CO 2 reaction. Important risks associated with gas humidity impact on solids consistency and desorber temperature impact on thermal degradation were explored, and adjustments to the bench-scale process were made to address those effects. Corrosion experiments were conducted to support selection of suitable materials of construction for the major unit operations in the process. The bench scale unit operations were assembled into

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

    PubMed

    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.

  2. Temporal characteristics of atmospheric CO2 in urban Nanjing, China

    NASA Astrophysics Data System (ADS)

    Huang, Xiaoxian; Wang, Tijian; Talbot, Robert; Xie, Min; Mao, Huiting; Li, Shu; Zhuang, Bingliang; Yang, Xiuqun; Fu, Congbin; Zhu, Jialei; Huang, Xing; Xu, Runying

    2015-02-01

    Although China is a big carbon dioxide (CO2) emitter, in situ measurements of atmospheric CO2 are sparse in urban China. The mixing ratio of carbon dioxide (CO2) and its influencing factors in urban Nanjing were investigated in this study, from the 18th of January to the 31st of December 2011. The annual average mixing ratio of CO2 was 406.5 ± 20.0 ppmv over the study period. The signal analysis using the fast Fourier transform (FFT) algorithm showed that CO2 had different cycles as a result of multiple controlling factors. The seasonal and intra-seasonal fluctuations of CO2 were mainly caused by the terrestrial biospheric uptake and emission and atmospheric oscillation. The weekly variation of CO2 was largely influenced by traffic volume. The diurnal cycle of CO2 presented a bimodal pattern in winter (DJF) probably due to the rush hour emissions. The seasonal mean CO2/CO correlation slope varied from 0.024 ppmv/ppbv to 0.029 ppmv/ppbv, comparable to the fossil fuel combustion emission ratio. The diurnal pattern of CO2/CO was irregular, indicating random anthropogenic emissions in an urban area. Firework setting was a large source of CO2 during the Spring Festival holiday. The backward trajectories by the HYSPLIT model showed that the local anthropogenic emissions contributed the most to the high CO2 mixing ratio in the urban area.

  3. 2-micron Double Pulsed IPDA Lidar for Atmospheric CO2 Measurement

    NASA Astrophysics Data System (ADS)

    Yu, Jirong; Petros, Mulugeta; Refaat, Tamer; Reithmaier, Karl; Remus, Ruben; Singh, Upendra; Johnson, Will; Boyer, Charlie; Fay, James; Johnston, Susan; Murchison, Luke; Scola, Tory

    2015-04-01

    We have developed a high energy pulsed 2-micron IPDA lidar instrument to measure the atmospheric CO2 column density. The IPDA lidar is operated on the long wavelength wing of R(30) CO2 line at 2050.967 nm (4875.749 cm-1) in the side-line operation mode. The R(30) line is an excellent absorption line for the measurements of CO2 in 2µm wavelength region with regard to the strength of the absorption lines, low susceptibility to atmospheric temperature variability, and freedom from problematic interference with other absorption lines. The Ho:Tm:YLF laser transmitter is designed to be operated in a unique double pulse format that can produce two-pulse pair in 10 Hz operation. Typically, the output energies of the laser transmitter are 100mJ and 45mJ for the first pulse and the second pulse, respectively. We injection seed the first pulse with on-line frequency and the second pulse with off-line frequency. The IPDA lidar instrument size, weight and power consumption were restricted to small research aircraft payload requirements. The airborne IPDA lidar instrument measures the total integrated column content of CO2 from the instrument to the ground but with weighting that can be tuned by controlling the transmitted wavelengths. 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. The 2-μm CO2 IPDA lidar airborne demonstration was conducted during March 20, 2014 through April 10, 2014. IPDA lidar airborne flights included various operating and environmental conditions. Environmental conditions included different flight altitude up to 8.3 km, different ground target conditions such as vegetation, soil, ocean, snow and sand and different cloud conditions. Besides, some flights targeted power plant incinerators for investigating the IPDA sensitivity to CO2 plums. The lidar instrument is robust during all of the flights. This paper describes

  4. Carbon-coated CoFe–CoFe2O4 composite particles with high and dual-band electromagnetic wave absorbing properties

    NASA Astrophysics Data System (ADS)

    Guan, Zhen-Jie; Jiang, Jian-Tang; Chen, Na; Gong, Yuan-Xun; Zhen, Liang

    2018-07-01

    SiO2 and TiO2, as conventional dielectric shells of ferromagnetic/dielectric composite particles, can protect ferromagnetic particles from aggregation and oxidation, but contribute little to electromagnetic loss. In this work, we designed nano-assembled CoFe–CoFe2O4@C composite particles, in which ferrites with high permeability were dielectric elements and carbon was introduced as protective layers, aiming for high-efficiency microwave absorption. These assembled particles with different CoFe contents were prepared through solvothermal methods and subsequent hydrogen-thermal reduction. CoFe nanoparticles were dispersed on a CoFe2O4 matrix via an in situ reduction transformation from CoFe2O4 to CoFe. The microstructure evolution of composite particles and corresponding electromagnetic properties tailoring were investigated. The content and size of CoFe as well as the porosity of composite particles increase gradually as the annealing temperature increases. A maximum reflection loss (RL max) of –71.73 dB is observed at 4.78 GHz in 3.4 mm thick coating using particles annealed at 500 °C as fillers. The coating presents double-band absorbing characteristics, as broad effective absorption bandwidth with RL > 5 (ERL 5) and high RL max are observed in both S-C and X-Ku bands. The tunability as well as the assembled characteristic of the electromagnetic property that endued from the composite structure contributes to the excellent electromagnetic wave absorbing performances.

  5. Carbon-coated CoFe-CoFe2O4 composite particles with high and dual-band electromagnetic wave absorbing properties.

    PubMed

    Guan, Zhen-Jie; Jiang, Jian-Tang; Chen, Na; Gong, Yuan-Xun; Zhen, Liang

    2018-07-27

    SiO 2 and TiO 2 , as conventional dielectric shells of ferromagnetic/dielectric composite particles, can protect ferromagnetic particles from aggregation and oxidation, but contribute little to electromagnetic loss. In this work, we designed nano-assembled CoFe-CoFe 2 O 4 @C composite particles, in which ferrites with high permeability were dielectric elements and carbon was introduced as protective layers, aiming for high-efficiency microwave absorption. These assembled particles with different CoFe contents were prepared through solvothermal methods and subsequent hydrogen-thermal reduction. CoFe nanoparticles were dispersed on a CoFe 2 O 4 matrix via an in situ reduction transformation from CoFe 2 O 4 to CoFe. The microstructure evolution of composite particles and corresponding electromagnetic properties tailoring were investigated. The content and size of CoFe as well as the porosity of composite particles increase gradually as the annealing temperature increases. A maximum reflection loss (RL max ) of -71.73 dB is observed at 4.78 GHz in 3.4 mm thick coating using particles annealed at 500 °C as fillers. The coating presents double-band absorbing characteristics, as broad effective absorption bandwidth with RL > 5 (ERL 5 ) and high RL max are observed in both S-C and X-K u bands. The tunability as well as the assembled characteristic of the electromagnetic property that endued from the composite structure contributes to the excellent electromagnetic wave absorbing performances.

  6. Speleothems as proxy for the carbon isotope composition of atmospheric CO2

    NASA Astrophysics Data System (ADS)

    Baskaran, M.; Krishnamurthy, R. V.

    1993-12-01

    We have measured the stable isotope ratios of carbon in a suite of recent cave deposits (less than 200 years) from the San Saba County, Texas, USA. The methodology for dating these deposits using excess Pb-210 was recently established (Baskaran and Iliffe, 1993). The carbon isotope ratios of these samples, spanning the time period approximately 1800-1990 AD, reflect the carbon isotope ratio of atmospheric CO2 for the same period. The pathways by which the delta C-13 of atmospheric CO2 is imprinted on these speleothems can be explained using a model developed by Cerling (1984). The results suggest that the carbon isotope ratios of speleothems can be used to develop long-term, high-resolution chronologies of the delta C-13 of atmospheric CO2 and, by implication, the concentration of the atmospheric CO2.

  7. Analysis of possible future atmospheric retention of fossil fuel CO/sub 2/

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Edmonds, J.A.; Reilly, J.; Trabalka, J.R.

    1984-09-01

    This report investigates the likely rates and the potential range of future CO/sub 2/ emissions, combined with knowledge of the global cycle of carbon, to estimate a possible range of future atmospheric CO/sub 2/ concentrations through the year 2075. Historic fossil fuel usage to the present, growing at a rate of 4.5% per year until 1973 and at a slower rate of 1.9% after 1973, was combined with three scenarios of projected emissions growth ranging from approximately 0.2 to 2.8% per year to provide annual CO/sub 2/ emissions data for two different carbon cycle models. The emissions scenarios were constructedmore » using an energy-economic model and by varying key parameters within the bounds of currently expected future values. The extreme values for CO/sub 2/ emissions in the year 2075 are 6.8 x 10/sup 15/ and 91 x 10/sup 15/ g C year/sup -1/. Carbon cycle model simulations used a range of year - 1800 preindustrial atmospheric concentrations of 245 to 292 ppM CO/sub 2/ and three scenarios of bioshere conversion as additional atmospheric CO/sub 2/ source terms. These simulations yield a range of possible atmospheric CO/sub 2/ concentrations in year 2075 of approximately 500 to 1500 ppM, with a median of about 700 ppM. The time at which atmospheric CO/sub 2/ would potentially double from the preindustrial level ranges from year 2025 to >2075. The practical, programmatic value of this forecast exercise is that it forces quantitative definition of the assumptions, and the uncertainties therein, which form the basis of our understanding of the natural biogeochemical cycle of carbon and both historic and future human influences on the dynamics of the global cycle. Assumptions about the possible range of future atmospheric CO/sub 2/ levels provide a basis on which to evaluate the implications of these changes on climate and the biosphere. 44 references, 17 figures, 21 tables.« less

  8. State of the Carbon Cycle - Consequences of Rising Atmospheric CO2

    NASA Astrophysics Data System (ADS)

    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

  9. State of the Carbon Cycle - Consequences of Rising Atmospheric CO2

    NASA Technical Reports Server (NTRS)

    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; hide

    2016-01-01

    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

  10. The role of artificial atmospheric CO2 removal in stabilizing Earth's climate

    NASA Astrophysics Data System (ADS)

    Zickfeld, K.; Tokarska, K.

    2014-12-01

    The current CO2 emission trend entails a risk that the 2°C target will be missed, potentially causing "dangerous" changes in Earth's climate system. This research explores the role of artificial atmospheric CO2 removal (also referred to as "negative emissions") in stabilizing Earth's climate after overshoot. We designed a range of plausible CO2 emission scenarios, which follow a gradual transition from a fossil fuel driven economy to a zero-emission energy system, followed by a period of negative emissions. The scenarios differ in peak emissions rate and, accordingly, the amount of negative emissions, to reach the same cumulative emissions compatible with the 2°C temperature stabilization target. The climate system components' responses are computed using the University of Victoria Earth System Climate Model of intermediate complexity. Results suggest that negative emissions are effective in reversing the global mean temperature and stabilizing it at a desired level (2°C above pre-industrial) after overshoot. Also, changes in the meridional overturning circulation and sea ice are reversible with the artificial removal of CO2 from the atmosphere. However, sea level continues to rise and is not reversible for several centuries, even under assumption of large amounts of negative emissions. For sea level to decline, atmospheric CO2 needs to be reduced to pre-industrial levels in our simulations. During the negative emission phase, outgassing of CO2 from terrestrial and marine carbon sinks offsets the artificial removal of atmospheric CO2, thereby reducing its effectiveness. On land, the largest CO2 outgassing occurs in the Tropics and is partially compensated by CO2 uptake at northern high latitudes. In the ocean, outgassing occurs mostly in the Southern Ocean, North Atlantic and tropical Pacific. The strongest outgassing occurs for pathways entailing greatest amounts of negative emissions, such that the efficiency of CO2 removal - here defined as the change in

  11. Biosequestration of atmospheric CO2 and flue gas-containing CO2 by microalgae.

    PubMed

    Cheah, Wai Yan; Show, Pau Loke; Chang, Jo-Shu; Ling, Tau Chuan; Juan, Joon Ching

    2015-05-01

    The unceasing rise of greenhouse gas emission has led to global warming and climate change. Global concern on this phenomenon has put forward the microalgal-based CO2 sequestration aiming to sequester carbon back to the biosphere, ultimately reducing greenhouse effects. Microalgae have recently gained enormous attention worldwide, to be the valuable feedstock for renewable energy production, due to their high growth rates, high lipid productivities and the ability to sequester carbon. The photosynthetic process of microalgae uses atmospheric CO2 and CO2 from flue gases, to synthesize nutrients for their growth. In this review article, we will primarily discuss the efficiency of CO2 biosequestration by microalgae species, factors influencing microalgal biomass productions, microalgal cultivation systems, the potential and limitations of using flue gas for microalgal cultivation as well as the bio-refinery approach of microalgal biomass. Copyright © 2014 Elsevier Ltd. All rights reserved.

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

    NASA Astrophysics Data System (ADS)

    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

  13. Evaluation of terrestrial carbon cycle models with atmospheric CO2 measurements: Results from transient simulations considering increasing CO2, climate, and land-use effects

    USGS Publications Warehouse

    Dargaville, R.J.; Heimann, Martin; McGuire, A.D.; Prentice, I.C.; Kicklighter, D.W.; Joos, F.; Clein, Joy S.; Esser, G.; Foley, J.; Kaplan, J.; Meier, R.A.; Melillo, J.M.; Moore, B.; Ramankutty, N.; Reichenau, T.; Schloss, A.; Sitch, S.; Tian, H.; Williams, L.J.; Wittenberg, U.

    2002-01-01

    An atmospheric transport model and observations of atmospheric CO2 are used to evaluate the performance of four Terrestrial Carbon Models (TCMs) in simulating the seasonal dynamics and interannual variability of atmospheric CO2 between 1980 and 1991. The TCMs were forced with time varying atmospheric CO2 concentrations, climate, and land use to simulate the net exchange of carbon between the terrestrial biosphere and the atmosphere. The monthly surface CO2 fluxes from the TCMs were used to drive the Model of Atmospheric Transport and Chemistry and the simulated seasonal cycles and concentration anomalies are compared with observations from several stations in the CMDL network. The TCMs underestimate the amplitude of the seasonal cycle and tend to simulate too early an uptake of CO2 during the spring by approximately one to two months. The model fluxes show an increase in amplitude as a result of land-use change, but that pattern is not so evident in the simulated atmospheric amplitudes, and the different models suggest different causes for the amplitude increase (i.e., CO2 fertilization, climate variability or land use change). The comparison of the modeled concentration anomalies with the observed anomalies indicates that either the TCMs underestimate interannual variability in the exchange of CO2 between the terrestrial biosphere and the atmosphere, or that either the variability in the ocean fluxes or the atmospheric transport may be key factors in the atmospheric interannual variability.

  14. Measurement of Concentration of CO2 in Atmosphere In Situ Based on TDLAS

    NASA Astrophysics Data System (ADS)

    Xin, Fengxin; Guo, Jinjia; Chen, Zhen; Liu, Zhishen

    2014-11-01

    As one of the main greenhouse gases in the atmosphere, CO2 has a significant impact on global climate change and the ecological environment. Because of close relationship between human activities and the CO2 emissions, it is very meaningful of detecting atmospheric CO2 accurately. Based on the technology of tunable diode laser absorption spectroscopy, the wavelength of distributed feedback laser is modulated, Fresnel lens is used as the receiving optical system, which receives the laser-beam reflected by corner reflector, and focuses the receiving laser-beam to the photoelectric detector. The second harmonic signal is received through lock-in amplifier and collected by AD data acquisition card, after that the system is built up. By choosing the infrared absorption line of CO2 at 1.57μm, the system is calibrated by 100% CO2 gas cell. The atmospheric CO2 in situ is measured with long open-path way. Furthermore, the results show that CO2 concentration decreases along time in the morning of day. It is proved that TDLAS technology has many advantages, including fast response, high sensitivity and resolution. This research provides a technique for monitoring secular change of CO2 in atmosphere.

  15. Measurement of Concentration of CO2 in Atmosphere In Situ Based on TDLAS

    NASA Astrophysics Data System (ADS)

    Xin, Fengxin; Guo, Jinjia; Chen, Zhen; Liu, Zhishen

    2014-11-01

    As one of the main greenhouse gases in the atmosphere, CO2has a significant impact on global climate change and the ecological environment. Because of close relationship between human activities and the CO2 emissions, it is very meaningful of detecting atmospheric CO2accurately. Based on the technology of tunable diode laser absorption spectroscopy, the wavelength of distributed feedback laser is modulated, Fresnel lens is used as the receiving optical system, which receives the laser-beam reflected by corner reflector, and focuses the receiving laser-beam to the photoelectric detector. The second harmonic signal is received through lock-in amplifier and collected by AD data acquisition card, after that the system is built up.By choosing the infrared absorption line of CO2at 1.57μm, the system is calibrated by 100% CO2 gas cell. The atmospheric CO2 in situ is measured with long open-path way. Furthermore, the results show that CO2 concentration decreases along time in the morning of day. It is proved that TDLAS technology has many advantages, including fast response, high sensitivity and resolution. This research provides a technique for monitoring secular change of CO2 in atmosphere.

  16. Modern soil system constraints on reconstructing deep-time atmospheric CO2

    NASA Astrophysics Data System (ADS)

    Montañez, Isabel P.

    2013-01-01

    Paleosol carbonate-based estimates of paleo-atmospheric CO2 play a prominent role in constraining radiative-forcing and climate sensitivity in the deep-time. Large uncertainty in paleo-CO2 estimates made using the paleosol-carbonate CO2-barometer, however, arises primarily from their sensitivity to soil-respired CO2 (S(z)). This parameter is poorly constrained due to a paucity of soil CO2 measurements during carbonate formation in modern soils and a lack of widely applicable proxies of paleo-soil CO2. Here the δ13C values of carbonate and soil organic matter (SOM) pairs from 130 Holocene soils are applied to a two-component CO2-mixing equation to define soil order-specific ranges of soil CO2 applicable for constraining S(z) in their corresponding paleosol analogs. Equilibrium carbonate-SOM pairs, characterized by Δ13Ccarb-SOM values of 12.2-15.8‰, define a mean effective fractionation of 14.1‰ and overall inferred total soil CO2 contents during calcite formation of <1000-10,000 ppmv. For those Aridisols and Alfisols, characterized by a net soil-moisture deficit, and their paleosol analogs (Calcisols and Argillisols), a best estimate of S(z) during calcite formation is 1500-2000 ppmv (range of 500-2500 ppmv). Overall higher values (2000-5000 ppmv) are indicated by the subset of these soils characterized by higher moisture content and productivity. Near atmospheric levels (400 ± 200 ppmv) of estimated S(z) are indicated by immature soils, recording their low soil productivity. Vertisols define the largest range in total soil CO2 (<1000 to >25,000 ppmv) reflecting their seasonally driven dynamic hydrochemistry. A S(z) range of 1000-10,000 ppmv is suggested for paleo-Vertisols for which calcite precipitation can be constrained to have occurred in an open system with two-component CO2 mixing, with a best estimate of 2000 ppmv ± 1000 ppmv appropriate for paleo-Vertisols for which evidence of protracted water saturation is lacking. Mollisol pairs define a best

  17. Assessing fossil fuel CO2 emissions in California using atmospheric observations and models

    NASA Astrophysics Data System (ADS)

    Graven, H.; Fischer, M. L.; Lueker, T.; Jeong, S.; Guilderson, T. P.; Keeling, R. F.; Bambha, R.; Brophy, K.; Callahan, W.; Cui, X.; Frankenberg, C.; Gurney, K. R.; LaFranchi, B. W.; Lehman, S. J.; Michelsen, H.; Miller, J. B.; Newman, S.; Paplawsky, W.; Parazoo, N. C.; Sloop, C.; Walker, S. J.

    2018-06-01

    Analysis systems incorporating atmospheric observations could provide a powerful tool for validating fossil fuel CO2 (ffCO2) emissions reported for individual regions, provided that fossil fuel sources can be separated from other CO2 sources or sinks and atmospheric transport can be accurately accounted for. We quantified ffCO2 by measuring radiocarbon (14C) in CO2, an accurate fossil-carbon tracer, at nine observation sites in California for three months in 2014–15. There is strong agreement between the measurements and ffCO2 simulated using a high-resolution atmospheric model and a spatiotemporally-resolved fossil fuel flux estimate. Inverse estimates of total in-state ffCO2 emissions are consistent with the California Air Resources Board’s reported ffCO2 emissions, providing tentative validation of California’s reported ffCO2 emissions in 2014–15. Continuing this prototype analysis system could provide critical independent evaluation of reported ffCO2 emissions and emissions reductions in California, and the system could be expanded to other, more data-poor regions.

  18. Production and uses of liquefied atmosphere (CO2) on Mars

    NASA Technical Reports Server (NTRS)

    Waldron, R. D.

    1991-01-01

    Carbon dioxide is universally accessible on Mars, and can be liquefied and separated from residual atmospheric gases by various compress-refrigeration cycles. Liquid CO2, stored under elevated pressures, can be used as a source of high pressure gas for nighttime power generation at a Martian base powered by solar energy during the daytime. Carbon dioxide can also be used for vehicular power. The extractable energy per unit mass of CO2 can exceed that of commercial lead-acid batteries for operating cycles without heat addition. Improved performance is possible using heat input from the ambient atmosphere or thermochemical agents. A unique vehicular application uses pressurized CO2 as a non-combustion low performance propellant for intermediate distance surface transportation. The thermodynamic properties of CO2 are presented with typical operating cycles for the application classes described above.

  19. Projected land photosynthesis constrained by changes in the seasonal cycle of atmospheric CO2.

    PubMed

    Wenzel, Sabrina; Cox, Peter M; Eyring, Veronika; Friedlingstein, Pierre

    2016-10-27

    Uncertainties in the response of vegetation to rising atmospheric CO 2 concentrations contribute to the large spread in projections of future climate change. Climate-carbon cycle models generally agree that elevated atmospheric CO 2 concentrations will enhance terrestrial gross primary productivity (GPP). However, the magnitude of this CO 2 fertilization effect varies from a 20 per cent to a 60 per cent increase in GPP for a doubling of atmospheric CO 2 concentrations in model studies. Here we demonstrate emergent constraints on large-scale CO 2 fertilization using observed changes in the amplitude of the atmospheric CO 2 seasonal cycle that are thought to be the result of increasing terrestrial GPP. Our comparison of atmospheric CO 2 measurements from Point Barrow in Alaska and Cape Kumukahi in Hawaii with historical simulations of the latest climate-carbon cycle models demonstrates that the increase in the amplitude of the CO 2 seasonal cycle at both measurement sites is consistent with increasing annual mean GPP, driven in part by climate warming, but with differences in CO 2 fertilization controlling the spread among the model trends. As a result, the relationship between the amplitude of the CO 2 seasonal cycle and the magnitude of CO 2 fertilization of GPP is almost linear across the entire ensemble of models. When combined with the observed trends in the seasonal CO 2 amplitude, these relationships lead to consistent emergent constraints on the CO 2 fertilization of GPP. Overall, we estimate a GPP increase of 37 ± 9 per cent for high-latitude ecosystems and 32 ± 9 per cent for extratropical ecosystems under a doubling of atmospheric CO 2 concentrations on the basis of the Point Barrow and Cape Kumukahi records, respectively.

  20. Carbon isotope signature of dissolved inorganic carbon (DIC) in precipitation and atmospheric CO2.

    PubMed

    Górka, Maciej; Sauer, Peter E; Lewicka-Szczebak, Dominika; Jędrysek, Mariusz-Orion

    2011-01-01

    This paper describes results of chemical and isotopic analysis of inorganic carbon species in the atmosphere and precipitation for the calendar year 2008 in Wrocław (SW Poland). Atmospheric air samples (collected weekly) and rainwater samples (collected after rain episodes) were analysed for CO2 and dissolved inorganic carbon (DIC) concentrations and for δ13C composition. The values obtained varied in the ranges: atmospheric CO2: 337-448 ppm; δ13CCO2 from -14.4 to -8.4‰; DIC in precipitation: 0.6-5.5 mg dm(-3); δ13CDIC from -22.2 to +0.2‰. No statistical correlation was observed between the concentration and δ13C value of atmospheric CO2 and DIC in precipitation. These observations contradict the commonly held assumption that atmospheric CO2 controls the DIC in precipitation. We infer that DIC is generated in ambient air temperatures, but from other sources than the measured atmospheric CO2. The calculated isotopic composition of a hypothetical CO2 source for DIC forming ranges from -31.4 to -11.0‰, showing significant seasonal variations accordingly to changing anthropogenic impact and atmospheric mixing processes. Copyright © 2010 Elsevier Ltd. All rights reserved.

  1. Synchronous change of atmospheric CO2 and Antarctic temperature during the last deglacial warming.

    PubMed

    Parrenin, F; Masson-Delmotte, V; Köhler, P; Raynaud, D; Paillard, D; Schwander, J; Barbante, C; Landais, A; Wegner, A; Jouzel, J

    2013-03-01

    Understanding the role of atmospheric CO2 during past climate changes requires clear knowledge of how it varies in time relative to temperature. Antarctic ice cores preserve highly resolved records of atmospheric CO2 and Antarctic temperature for the past 800,000 years. Here we propose a revised relative age scale for the concentration of atmospheric CO2 and Antarctic temperature for the last deglacial warming, using data from five Antarctic ice cores. We infer the phasing between CO2 concentration and Antarctic temperature at four times when their trends change abruptly. We find no significant asynchrony between them, indicating that Antarctic temperature did not begin to rise hundreds of years before the concentration of atmospheric CO2, as has been suggested by earlier studies.

  2. Climatic consequences of very high CO2 levels in Earth's early atmosphere

    NASA Technical Reports Server (NTRS)

    Kasting, J. F.

    1985-01-01

    Earth has approximately 60 bars of carbon dioxide tied up in carbonate rocks, or roughly 2/3 the amount of CO2 of Venus' atmosphere. Two different lines of evidence, one based on thermodynamics and the other on geochemical cycles, indicate that a substantial fraction of this CO2 may have resulted in the atmosphere during the first few hundred million years of the Earth's history. A natural question which arises concerning this hypothesis is whether this would have resulted in a runaway greenhouse affect. One-dimensional radiative/convective model calculations show that the surface temperature of a hypothetical primitive atmosphere containing 20 bars of CO2 would have been less than 100C and no runaway greenhouse should have occurred. The climatic stability of the early atmosphere is a consequence of three factors: (1) reduced solar luminosity at that time; (2) an increase in planetary albedo caused by Rayleigh scattering by CO2; and (3) the stabilizing effects of moist convection. The latter two factors are sufficient to prevent a CO2-induced runaway greenhouse on the present Earth and for CO2 levels up to 100 bars. It is determined whether a runaway greenhouse could have occurred during the latter stages of the accretion process and, if so, whether it would have collapsed once the influx of material slowed down.

  3. Fast Atmosphere-Ocean Model Runs with Large Changes in CO2

    NASA Technical Reports Server (NTRS)

    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.

  4. Can increasing CO2 cool Antarctica?

    NASA Astrophysics Data System (ADS)

    Schmithuesen, Holger; Notholt, Justus; König-Langlo, Gert; Lemke, Peter

    2014-05-01

    CO2 is the strongest anthropogenic forcing agent for climate change since pre-industrial times. Like other greenhouse gases, CO2 absorbs terrestrial surface radiation and causes emission from the atmosphere to space. As the surface is generally warmer than the atmosphere, the total long-wave emission to space is commonly less than the surface emission. However, this does not hold true for the high elevated areas of central Antarctica. Our investigations show, that for the high elevated areas of Antarctica the greenhouse effect (GHE) of CO2 is commonly around zero or even negative. This is based on the quantification of GHE as the difference between long-wave surface emission and top of atmosphere emission. We demonstrate this behaviour with the help of three models: a simple two-layer model, line-by-line calculations, and an ECMWF experiment. Additionally, in this region an increase in CO2 concentration leads to an instantaneous increased long-wave energy loss to space, which is a cooling effect on the earth-atmosphere system. However, short-wave warming by the weak absorption of solar radiation by CO2 are not taken into account here. The reason for this counter-intuitive behaviour is the fact that in the interior of Antarctica the surface is often colder than the stratosphere above. Radiation from the surface in the atmospheric window emitted to space is then relatively lower compared to radiation in the main CO2 band around 15 microns, which originates mostly from the stratosphere. Increasing CO2 concentration leads to increasing emission from the atmosphere to space, while blocking additional portions of surface emission. If the surface is colder than the stratosphere, this leads to additional long-wave energy loss to space for increasing CO2. Our findings for central Antarctica are in strong contrast to the generally known effect that increasing CO2 has on the long-wave emission to space, and hence on the Antarctic climate.

  5. CO2 capture from humid flue gases and humid atmosphere using a microporous coppersilicate.

    PubMed

    Datta, Shuvo Jit; Khumnoon, Chutharat; Lee, Zhen Hao; Moon, Won Kyung; Docao, Son; Nguyen, Thanh Huu; Hwang, In Chul; Moon, Dohyun; Oleynikov, Peter; Terasaki, Osamu; Yoon, Kyung Byung

    2015-10-16

    Capturing CO2 from humid flue gases and atmosphere with porous materials remains costly because prior dehydration of the gases is required. A large number of microporous materials with physical adsorption capacity have been developed as CO2-capturing materials. However, most of them suffer from CO2 sorption capacity reduction or structure decomposition that is caused by co-adsorbed H2O when exposed to humid flue gases and atmosphere. We report a highly stable microporous coppersilicate. It has H2O-specific and CO2-specific adsorption sites but does not have H2O/CO2-sharing sites. Therefore, it readily adsorbs both H2O and CO2 from the humid flue gases and atmosphere, but the adsorbing H2O does not interfere with the adsorption of CO2. It is also highly stable after adsorption of H2O and CO2 because it was synthesized hydrothermally. Copyright © 2015, American Association for the Advancement of Science.

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

    NASA Astrophysics Data System (ADS)

    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

  7. A joint data assimilation system (Tan-Tracker) to simultaneously estimate surface CO2 fluxes and 3-D atmospheric CO2 concentrations from observations

    NASA Astrophysics Data System (ADS)

    Tian, X.; Xie, Z.; Liu, Y.; Cai, Z.; Fu, Y.; Zhang, H.; Feng, L.

    2014-12-01

    We have developed a novel framework ("Tan-Tracker") for assimilating observations of atmospheric CO2 concentrations, based on the POD-based (proper orthogonal decomposition) ensemble four-dimensional variational data assimilation method (PODEn4DVar). The high flexibility and the high computational efficiency of the PODEn4DVar approach allow us to include both the atmospheric CO2 concentrations and the surface CO2 fluxes as part of the large state vector to be simultaneously estimated from assimilation of atmospheric CO2 observations. Compared to most modern top-down flux inversion approaches, where only surface fluxes are considered as control variables, one major advantage of our joint data assimilation system is that, in principle, no assumption on perfect transport models is needed. In addition, the possibility for Tan-Tracker to use a complete dynamic model to consistently describe the time evolution of CO2 surface fluxes (CFs) and the atmospheric CO2 concentrations represents a better use of observation information for recycling the analyses at each assimilation step in order to improve the forecasts for the following assimilations. An experimental Tan-Tracker system has been built based on a complete augmented dynamical model, where (1) the surface atmosphere CO2 exchanges are prescribed by using a persistent forecasting model for the scaling factors of the first-guess net CO2 surface fluxes and (2) the atmospheric CO2 transport is simulated by using the GEOS-Chem three-dimensional global chemistry transport model. Observing system simulation experiments (OSSEs) for assimilating synthetic in situ observations of surface CO2 concentrations are carefully designed to evaluate the effectiveness of the Tan-Tracker system. In particular, detailed comparisons are made with its simplified version (referred to as TT-S) with only CFs taken as the prognostic variables. It is found that our Tan-Tracker system is capable of outperforming TT-S with higher assimilation

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

    NASA Astrophysics Data System (ADS)

    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

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

    NASA Astrophysics Data System (ADS)

    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

  10. Analysis of Vertical Weighting Functions for Lidar Measurements of Atmospheric CO2 and O2

    NASA Astrophysics Data System (ADS)

    Kooi, S.; Mao, J.; Abshire, J. B.; Browell, E. V.; Weaver, C. J.; Kawa, S. R.

    2011-12-01

    Several NASA groups have developed integrated path differential absorption (IPDA) lidar approaches to measure atmospheric CO2 concentrations from space as a candidates for NASA's ASCENDS space mission. For example, the Goddard CO2 Sounder approach uses two pulsed lasers to simultaneously measure both CO2 and O2 absorption in the vertical path to the surface at a number of wavelengths across a CO2 line near 1572 nm and an O2 line doublet near 764 nm. The measurements of CO2 and O2 absorption allow computing their vertically weighted number densities and then their ratios for estimating CO2 concentration relative to dry air. Since both the CO2 and O2 densities and their absorption line-width decrease with altitude, the absorption response (or weighting function) varies with both altitude and absorption wavelength. We have used some standard atmospheres and HITRAN 2008 spectroscopy to calculate the vertical weighting functions for two CO2 lines near 1571 nm and the O2 lines near 764.7 and 1260 nm for candidate online wavelength selections for ASCENDS. For CO2, the primary candidate on-line wavelengths are 10-12 pm away from line center with the weighting function peaking in the atmospheric boundary layer to measure CO2 sources and sinks at the surface. Using another on-line wavelength 3-5 pm away from line center allows the weighting function to peak in the mid- to upper troposphere, which is sensitive to CO2 transport in the free atmosphere. The Goddard CO2 sounder team developed an airborne precursor version of a space instrument. During the summers of 2009, 2010 and 2011 it has participated in airborne measurement campaigns over a variety of different sites in the US, flying with other NASA ASCENDS lidar candidates along with accurate in-situ atmospheric sensors. All flights used altitude patterns with measurements at steps in altitudes between 3 and 13 km, along with spirals from 13 km altitude to near the surface. Measurements from in-situ sensors allowed an

  11. Implications of high amplitude atmospheric CO2 fluctuations on past millennium climate change

    NASA Astrophysics Data System (ADS)

    van Hoof, Thomas; Kouwenberg, Lenny; Wagner-Cremer, Friederike; Visscher, Henk

    2010-05-01

    Stomatal frequency analysis of leaves of land plants preserved in peat and lake deposits can provide a proxy record of pre-industrial atmospheric CO2 concentration complementary to measurements in Antarctic ice cores. Stomatal frequency based CO2 trends from the USA and NW European support the presence of significant CO2 variability during the first half of the last millennium (Kouwenberg et al., 2005; Wagner et al., 2004; van Hoof et al., 2008). The timing of the most significant perturbation in the stomata records (1200 AD) is in agreement with an observed CO2 fluctuation in the D47 Antarctic ice-core record (Barnola et al., 1995; van Hoof et al., 2005). The amplitude of the stomatal frequency based CO2 changes (> 34ppmv) exceeds the maximum amplitude of CO2 variability in the D47 ice core (< 10 ppmv). A modelling experiment taking into account firn-densification based smoothing processes in the D47 ice core proved, however, that the amplitude difference between the stomata record and the D47 ice-core can be explained by natural smoothing processes in the ice (van Hoof et al., 2005). This observation gives credence to the existence of high-amplitude CO2 fluctuations during the last millennium and suggests that high resolution ice core CO2 records should be regarded as a smoothed representation of the atmospheric CO2 signal. In the present study, potential marine and terrestrial sources and sinks associated with the observed atmospheric CO2 perturbation will be discussed. The magnitude of the observed CO2 variability implies that inferred changes in CO2 radiative forcing are of a similar magnitude as variations ascribed to other forcing mechanisms (e.g. solar forcing and volcanism), therefore challenging the IPCC concept of CO2 as an insignificant preindustrial climate forcing factor. References Barnola J.M., M. Anklin, J. Porcheron, D. Raynaud, J. Schwander and B. Stauffer 1995. CO2 evolution during the last millennium as recorded by Antarctic and Greenland ice

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

    PubMed

    Fernández-Martínez, M; Vicca, S; Janssens, I A; Ciais, P; Obersteiner, M; Bartrons, M; Sardans, J; Verger, A; Canadell, J G; Chevallier, F; Wang, X; Bernhofer, C; Curtis, P S; Gianelle, D; Grünwald, T; Heinesch, B; Ibrom, A; Knohl, A; Laurila, T; Law, B E; Limousin, J M; Longdoz, B; Loustau, D; Mammarella, I; Matteucci, G; Monson, R K; Montagnani, L; Moors, E J; Munger, J W; Papale, D; Piao, S L; Peñuelas, J

    2017-08-29

    Concentrations of atmospheric carbon dioxide (CO 2 ) 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 generalised mixed models, we found that forest-level net ecosystem production and gross primary production have increased by 1% annually from 1995 to 2011. Statistical models indicated that increasing atmospheric CO 2 was the most important factor driving the increasing strength of carbon sinks in these forests. We also found that the reduction of sulphur deposition in Europe and the USA lead to higher recovery in ecosystem respiration than in gross primary production, thus limiting the increase of carbon sequestration. By contrast, trends in climate and nitrogen deposition did not significantly contribute to changing carbon fluxes during the studied period. Our findings support the hypothesis of a general CO 2 -fertilization effect on vegetation growth and suggest that, so far unknown, sulphur deposition plays a significant role in the carbon balance of forests in industrialized regions. Our results show the need to include the effects of changing atmospheric composition, beyond CO 2 , to assess future dynamics of carbon-climate feedbacks not currently considered in earth system/climate modelling.

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

    PubMed

    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 ).

  14. Sensitivity Analysis for Atmospheric Infrared Sounder (AIRS) CO2 Retrieval

    NASA Technical Reports Server (NTRS)

    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.

  15. Atmospheric CO2 variations on millennial-scale during MIS 6

    NASA Astrophysics Data System (ADS)

    Shin, Jinhwa; Grilli, Roberto; Chappellaz, Jérôme; Teste, Grégory; Nehrbass-Ahles, Christoph; Schmidely, Loïc; Schmitt, Jochen; Stocker, Thomas; Fischer, Hubertus

    2017-04-01

    Understanding natural carbon cycle / climate feedbacks on various time scales is highly important for predicting future climate changes. Paleoclimate records of Antarctic temperatures, relative sea level and foraminiferal isotope and pollen records in sediment cores from the Portuguese margin have shown climate variations on millennial time scale over the Marine Isotope Stage 6 (MIS 6; from approximately 135 to 190 kyr BP). These proxy data suggested iceberg calving in the North Atlantic result in cooling in the Northern hemisphere and warming in Antarctica by changes in the Atlantic Meridional Overturning Circulation, which is explained by a bipolar see-saw trend in the ocean (Margari et al., 2010). Atmospheric CO2 reconstruction from Antarctic ice cores can provide key information on how atmospheric CO2 concentrations are linked to millennial-scale climate changes. However, existing CO2 records cannot be used to address this relationship because of the lack of suitable temporal resolution. In this work, we will present a new CO2 record with an improved time resolution, obtained from the Dome C ice core (75˚ 06'S, 123˚ 24'E) spanning the MIS 6 period, using dry extraction methods. We will examine millennial-scale features in atmospheric CO2, and their possible links with other proxies covering MIS 6. Margari, V., Skinner, L. C., Tzedakis, P. C., Ganopolski, A., Vautravers, M., and Shackleton, N. J.: The nature of millennial scale climate variability during the past two glacial periods, Nat.Geosci., 3, 127-131, 2010.

  16. Atmospheric inversion for cost effective quantification of city CO2 emissions

    NASA Astrophysics Data System (ADS)

    Wu, L.; Broquet, G.; Ciais, P.; Bellassen, V.; Vogel, F.; Chevallier, F.; Xueref-Remy, I.; Wang, Y.

    2015-11-01

    Cities, currently covering only a very small portion (< 3 %) of the world's land surface, directly release to the atmosphere about 44 % of global energy-related CO2, and 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 Monitoring, Reporting and Verification (MRV) procedures that play a key role for market- or policy-based mitigation actions. Here we propose 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. We examine the cost-effectiveness and the performance of such a tool. The instruments presently used to measure CO2 concentrations at research stations are expensive. However, cheaper sensors are currently developed and should be useable for the monitoring of CO2 emissions from a megacity in the near-term. Our assessment of the inversion method is thus based on the use of several types of hypothetical networks, with a range of numbers of sensors sampling at 25 m a.g.l. The study case for this assessment is the monitoring of the emissions of the Paris metropolitan area (~ 12 million inhabitants and 11.4 Tg C emitted in 2010) during the month of January 2011. The performance of the inversion is evaluated in terms of uncertainties in the estimates of total and sectoral CO2 emissions. These uncertainties are compared to a notional ambitious target to diagnose annual total city emissions with an uncertainty of 5 % (2-sigma). We find that, with 10 stations only, which is the typical size of current pilot networks that are deployed in some cities, the uncertainty for the 1-month total city CO2 emissions is significantly reduced by the inversion by ~ 42 % but still corresponds to an annual

  17. The Role of CO2 Clouds on the Stability of the Early Mars Atmosphere Against Collapse

    NASA Astrophysics Data System (ADS)

    Kahre, Melinda A.; Haberle, Robert; Steakley, Kathryn; Murphy, Jim; Kling, Alexandre

    2017-10-01

    The early Mars atmosphere was likely significantly more massive than it is today, given the growing body of evidence that liquid water flowed on the surface early in the planet’s history. Although the CO2 inventory was likely larger in the past, there is much we still do not understand about the state of that CO2. As surface pressure increases, the temperature at which CO2 condenses also increases, making it more likely that CO2 ice would form and persist on the surface when the atmospheric mass increases. An atmosphere that is stable against collapse must contain enough energy, distributed globally, to prohibit the formation of permanents CO2 ice reservoirs that lead to collapse. The presence of the “faint young sun” compounds this issue. Previous global climate model (GCM) investigations show that atmospheres within specific ranges of obliquities and atmospheric masses are stable against collapse. We use the NASA Ames Mars GCM to expand on these works by focusing specifically on the role of CO2 clouds in atmospheric stability. Two end member simulations are executed, one that includes CO2 cloud formation and one that does not. The simulation that explicitly includes CO2 clouds is stable, while the simulation without CO2 clouds collapses into permanent surface CO2 reservoirs. In both cases, significant atmospheric condensation is occurring in the atmosphere throughout the year. In the case without CO2 clouds, all atmospheric condensation (even if it occurs at altitude) leads directly to the accumulation of surface ice, whereas in the case with CO2 clouds, there is a finite settling timescale for the cloud particles. Depending on this timescale and the local conditions, the cloud particles could stay aloft or sublimate as they fall toward the surface. Thus, the striking difference between these two cases illustrates the important role of CO2 clouds. We plan to conduct and present further simulations to better understand how atmospheric stability depends on

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

    NASA Astrophysics Data System (ADS)

    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.

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

    PubMed Central

    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. PMID:26154449

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

    PubMed

    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.

  1. Deep Sea Memory of High Atmospheric CO2 Concentration

    NASA Astrophysics Data System (ADS)

    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

  2. Atmospheric CO2 Records from Sites in the Umweltbundesamt (UBA) Air Sampling Network (1972 - 1997)

    DOE Data Explorer

    Fricke, W. [Umweltbundesamt, Offenbach/Main, Germany; Wallasch, M. [Umweltbundesamt, Offenbach/Main, Germany; Uhse, Karin [Umweltbundesamt, Offenbach/Main, Germany; Schmidt, Martina [University of Heidelberg, Heidelberg, Germany; Levin, Ingeborg [University of Heidelberg, Heidelberg, Germany

    1998-01-01

    Air samples for the purpose of monitoring atmospheric CO2 were collected from five sites in the UBA air sampling network. Annual atmospheric CO2 concentrations at Brotjacklriegel rose from 331.63 parts per million by volume (ppmv) in 1972 to 353.12 ppmv in 1988. Because of the site's forest location, the monthly atmospheric CO2 record from Brotjacklriegel exhibits very large seasonal amplitude. This amplitude reached almost 40 ppmv in 1985. Minimum mixing ratios are recorded at Brotjacklriegel during July-September; maximum values, during November-March. CO2 concentrations at Deuselbach rose from 340.82 parts per million by volume (ppmv) in 1972 to 363.76 ppmv in 1989. The monthly atmospheric CO2 record from Deuselbach is influenced by local agricultural activities and photosynthetic depletion but does not exhibit the large seasonal amplitude observed at other UBA monitoring sites. Minimum monthly atmospheric CO2 mixing ratios at Deuselbach are typically observed in August but may appear as early as June. Maximum values are seen in the record for November-March. Atmospheric CO2 concentrations at Schauinsland rose from ~328 parts per million by volume (ppmv) in 1972 to ~365 ppmv in 1997. This represents a growth rate of approximately 1.5 ppmv per year. The Schauinsland site is considered the least contaminated of the UBA sites. CO2 concentrations at Waldhof rose from 346.82 parts per million by volume (ppmv) in 1972 to 372.09 ppmv in 1993. The Waldhof site is subject to pollution sources; consequently, the monthly atmospheric CO2 record exhibits a large seasonal amplitude. Atmospheric CO2 concentrations at Westerland rose from ~329 parts per million by volume (ppmv) in 1973 to ~364 ppmv in 1997. The atmospheric CO2 record from Westerland shows a seasonal pattern similar to other UBA sites; minimum values are recorded during July-September; maximum mixing ratios during November-March.

  3. Long-term measurements of atmospheric trace gases (CO2, CH4, N2O, SF6, CO, H2), O2, and δ13CH4 isotopes at Weybourne Atmospheric Observatory, UK: past, present and future

    NASA Astrophysics Data System (ADS)

    Manning, Andrew C.; Forster, Grant L.; Oram, David E.; Reeves, Claire E.; Pickers, Penelope A.; Barningham, S. Thomas; Sturges, William T.; Bandy, Brian; Nisbet, Euan G.; Lowry, David; Fisher, Rebecca; Fleming, Zoe

    2016-04-01

    The Weybourne Atmospheric Observatory (WAO) is situated on the north Norfolk Coast (52.95°N, 1.13°E) in the United Kingdom and is run by the University of East Anglia (UEA), with support from the UK National Centre for Atmospheric Science (NCAS). In 2016, the WAO became a UK-ICOS (Integrated Carbon Observing System) monitoring station. Since 2008, we have been collecting high-precision long-term in situ measurements of atmospheric carbon dioxide (CO2), oxygen (O2), carbon monoxide (CO) and molecular hydrogen (H2), as well as regular bag sampling for δ13CH4. In early 2013, the measurement of atmospheric methane (CH4) commenced, and nitrous oxide (N2O) and sulphur hexafluoride (SF6) began in 2014. We summarise the CO2, O2, CH4, N2O, SF6, CO, H2 and δ13CH4 measurements made to date and highlight some key features observed (e.g. seasonal cycles, long-term trends, pollution events and deposition events). We summarise how the long-term measurements fit into other broader projects which have helped to support the long term time-series at WAO over the years, and highlight how we contribute to broader global atmospheric observation networks.

  4. Stability of CO2 Atmospheres on Terrestrial Exoplanets in the Proximity of M Dwarfs

    NASA Astrophysics Data System (ADS)

    Gao, P.; Hu, R.; Yung, Y. L.

    2013-12-01

    M dwarfs are promising targets for the search and characterization of terrestrial exoplanets that might be habitable, as the habitable planets around M dwarfs are in much more close-in orbits compared to their counterparts around Sun-like stars. CO2, one of the most important greenhouse gases on our planet, is conventionally adopted as a major greenhouse gas in studying the habitability of terrestrial exoplanets around M dwarfs. However, the stability of CO2 in terrestrial atmospheres has been called into question due to the high FUV/NUV flux ratio of some M dwarfs in comparison to that of Sun-like stars. While CO2 is photolyzed into CO and O by photons in the FUV, with O2 forming from the O atoms through third body catalytic reactions, NUV photons are able to photolyze water, producing HOx radicals which go on to catalytically recombine the relatively stable CO and O2 molecules back into CO2. The comparatively low NUV flux of some M dwarfs leads to a significantly reduced efficiency of catalytic recombination of CO and O2 and the possible net destruction of CO2 and the build up of CO and O2. In this work we test the above hypothesis using a 1D photochemical kinetics model for a Mars-sized planet with an initial atmospheric composition similar to that of Mars and the incoming stellar flux of a weakly active M dwarf, assuming the exoplanet is 0.1 AU away from its parent star, in proximity of its habitable zone. We show that a CO2-dominated atmosphere can be converted into a CO2/CO/O2-dominated atmosphere in 10^3-10^4 years by CO2 photolysis. This process is kept from running away by a combination of O2 photolysis, three body reactions of O, O2, and another species to form O3, and reactions of CO with OH to form CO2 and H. However, such a large amount of O2 and CO, combined with some amount of H and H2, may be susceptible to spontaneous combustion or detonation, and thus could prove to be an especially unstable state in itself. Thus there could arise a situation

  5. Regional and Global Atmospheric CO2 Measurements Using 1.57 Micron IM-CW Lidar

    NASA Technical Reports Server (NTRS)

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

    2015-01-01

    Atmospheric CO2 is a critical forcing for the Earth's climate, and knowledge of its distribution and variations influences predictions of the Earth's future climate. Accurate observations of atmospheric CO2 are also crucial to improving our understanding of CO2 sources, sinks and transports. To meet these science needs, NASA is developing technologies for the Active Sensing of CO2 Emissions over Nights, Days, and Seasons (ASCENDS) space mission, which is aimed at global CO2 observations. Meanwhile an airborne investigation of atmospheric CO2 distributions as part of the NASA Suborbital Atmospheric Carbon and Transport â€" America (ACT-America) mission will be conducted with lidar and in situ instrumentation over the central and eastern United States during all four seasons and under a wide range of meteorological conditions. In preparing for the ASCENDS mission, NASA Langley Research Center and Exelis Inc./Harris Corp. have jointly developed and demonstrated the capability of atmospheric CO2 column measurements with an intensity-modulated continuous-wave (IM-CW) lidar. Since 2005, a total of 14 flight campaigns have been conducted. A measurement precision of approx.0.3 ppmv for a 10-s average over desert and vegetated surfaces has been achieved, and the lidar CO2 measurements also agree well with in-situ observations. Significant atmospheric CO2 variations on various spatiotemporal scales have been observed during these campaigns. For example, around 10-ppm CO2 changes were found within free troposphere in a region of about 200A-300 sq km over Iowa during a summer 2014 flight. Results from recent flight campaigns are presented in this paper. The ability to achieve the science objectives of the ASCENDS mission with an IM-CW lidar is also discussed in this paper, along with the plans for the ACT-America aircraft investigation that begins in the winter of 2016.

  6. Constraining land carbon cycle process understanding with observations of atmospheric CO2 variability

    NASA Astrophysics Data System (ADS)

    Collatz, G. J.; Kawa, S. R.; Liu, Y.; Zeng, F.; Ivanoff, A.

    2013-12-01

    We evaluate our understanding of the land biospheric carbon cycle by benchmarking a model and its variants to atmospheric CO2 observations and to an atmospheric CO2 inversion. Though the seasonal cycle in CO2 observations is well simulated by the model (RMSE/standard deviation of observations <0.5 at most sites north of 15N and <1 for Southern Hemisphere sites) different model setups suggest that the CO2 seasonal cycle provides some constraint on gross photosynthesis, respiration, and fire fluxes revealed in the amplitude and phase at northern latitude sites. CarbonTracker inversions (CT) and model show similar phasing of the seasonal fluxes but agreement in the amplitude varies by region. We also evaluate interannual variability (IAV) in the measured atmospheric CO2 which, in contrast to the seasonal cycle, is not well represented by the model. We estimate the contributions of biospheric and fire fluxes, and atmospheric transport variability to explaining observed variability in measured CO2. Comparisons with CT show that modeled IAV has some correspondence to the inversion results >40N though fluxes match poorly at regional to continental scales. Regional and global fire emissions are strongly correlated with variability observed at northern flask sample sites and in the global atmospheric CO2 growth rate though in the latter case fire emissions anomalies are not large enough to account fully for the observed variability. We discuss remaining unexplained variability in CO2 observations in terms of the representation of fluxes by the model. This work also demonstrates the limitations of the current network of CO2 observations and the potential of new denser surface measurements and space based column measurements for constraining carbon cycle processes in models.

  7. Rising global atmospheric CO2 concentration and implications for crop productivity

    USDA-ARS?s Scientific Manuscript database

    There is incontestable evidence that the concentration of atmospheric CO2 is increasing. Regardless of the potential impact of this increase on climate change, CO2 will have a direct effect on plants since it is a primary input for growth. Herein, we discuss relative CO2 responses of C3 and C4 plant...

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

    PubMed

    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.

  9. Development of a Coherent Differential Absorption Lidar for Range Resolved Atmospheric CO2 Measurements

    NASA Technical Reports Server (NTRS)

    Yu, Jirong; Petros, Mulgueta; Chen, Songsheng; Bai, Yingxin; Petzar, Paul J.; Trieu, Bo. C.; Koch, Grady J.; Beyon, Jeffery J.; Singh, Upendra N.

    2010-01-01

    A pulsed, 2-m coherent Differential Absorption Lidar (DIAL) / Integrated Path Differential Absorption (IPDA) transceiver, developed under the Laser Risk Reduction Program (LRRP) at NASA, is integrated into a fully functional lidar instrument. This instrument will measure atmospheric CO2 profiles (by DIAL) initially from a ground platform, and then be prepared for aircraft installation to measure the atmospheric CO2 column densities in the atmospheric boundary layer (ABL) and lower troposphere. The airborne prototype CO2 lidar can measure atmospheric CO2 column density in a range bin of 1km with better than 1.5% precision at horizontal resolution of less than 50km. It can provide the image of the pooling of CO2 in lowlying areas and performs nighttime mass balance measurements at landscape scale. This sensor is unique in its capability to study the vertical ABL-free troposphere exchange of CO2 directly. It will allow the investigators to pursue subsequent in science-driven deployments, and provides a unique tool for Active Sensing of CO2 Emissions over Night, Days, and Seasons (ASCENDS) validation that was strongly advocated in the recent ASCENDS Workshop.

  10. Atmospheric CO2 Concentration Measurements with Clouds from an Airborne Lidar

    NASA Astrophysics Data System (ADS)

    Mao, J.; Abshire, J. B.; Kawa, S. R.; Riris, H.; Allan, G. R.; Hasselbrack, W. E.; Numata, K.; Chen, J. R.; Sun, X.; DiGangi, J. P.; Choi, Y.

    2017-12-01

    Globally distributed atmospheric CO2 concentration measurements with high precision, low bias and full seasonal sampling are crucial to advance carbon cycle sciences. However, two thirds of the Earth's surface is typically covered by clouds, and passive remote sensing approaches from space are limited to cloud-free scenes. NASA Goddard is developing a pulsed, integrated-path differential absorption (IPDA) lidar approach to measure atmospheric column CO2 concentrations, XCO2, from space as a candidate for NASA's ASCENDS mission. Measurements of time-resolved laser backscatter profiles from the atmosphere also allow this technique to estimate XCO2 and range to cloud tops in addition to those to the ground with precise knowledge of the photon path-length. We demonstrate this measurement capability using airborne lidar measurements from summer 2017 ASCENDS airborne science campaign in Alaska. We show retrievals of XCO2 to ground and to a variety of cloud tops. We will also demonstrate how the partial column XCO2 to cloud tops and cloud slicing approach help resolving vertical and horizontal gradient of CO2 in cloudy conditions. The XCO2 retrievals from the lidar are validated against in situ measurements and compared to the Goddard Parameterized Chemistry Transport Model (PCTM) simulations. Adding this measurement capability to the future lidar mission for XCO2 will provide full global and seasonal data coverage and some information about vertical structure of CO2. This unique facility is expected to benefit atmospheric transport process studies, carbon data assimilation in models, and global and regional carbon flux estimation.

  11. Stable carbon isotope ratio in atmospheric CO2 collected by new diffusive devices.

    PubMed

    Proto, Antonio; Cucciniello, Raffaele; Rossi, Federico; Motta, Oriana

    2014-02-01

    In this paper, stable carbon isotope ratios (δ (13)C) were determined in the atmosphere by using a Ca-based sorbent, CaO/Ca12Al14O33 75:25 w/w, for passively collecting atmospheric CO2, in both field and laboratory experiments. Field measurements were conducted in three environments characterized by different carbon dioxide sources. In particular, the environments under consideration were a rather heavily trafficked road, where the source of CO2 is mostly vehicle exhaust, a rural unpolluted area, and a private kitchen where the major source of CO2 was gas combustion. Samplers were exposed to the free atmosphere for 3 days in order to allow collection of sufficient CO2 for δ(13)C analysis, then the collected CO2 was desorbed from the adsorbent with acid treatment, and directly analyzed by nondispersive infrared (NDIR) instrument. δ (13)C results confirmed that the samplers collected representative CO2 samples and no fractionation occurred during passive trapping, as also confirmed by an appositely designed experiment conducted in the laboratory. Passive sampling using CaO/Ca12Al14O33 75:25 w/w proved to be an easy and reliable method to collect atmospheric carbon dioxide for δ (13)C analysis in both indoor and outdoor places.

  12. High-O2, low-CO2 atmosphere on early Mars inferred from manganese oxide deposits

    NASA Astrophysics Data System (ADS)

    Sekine, Y.; Imanura, S.; Noda, N.; Takahashi, Y.; Uesugi, S.; Kurisu, M.; Hartmann, J.

    2017-12-01

    The atmospheric composition and its redox state are central to understanding of geochemical cycles, aqueous environment, and habitability on early Mars. Findings of manganese (Mn) oxide deposits together with some trace metals (e.g., Zn and Ni) by the Curiosity and Opportunity rovers suggest a more oxidizing surface environments on early Mars, possibly with higher amount of O2, than in the present day [Lanza et al., 2016; Arvidson et al., 2016; Hurowitz et al., 2017]. However, the abundance and formation mechanism of O2 have been poorly constrained. In the present study, we report results of laboratory experiments to constrain the redox state of the aqueous environment and atmospheric composition responsible for formation of the Mn oxides on early Mars. Our results of scavenging pattern of trace metals show that the Mn oxides found by the rovers are MnO2, which requires highly oxidizing water (Eh > 0.4 V at pH 7-8) and high atmospheric O2 (> a few mbar) for deposition. We suggest that a low-CO2 condition are also required to prevent formation of Mn carbonate in the aqueous environments. We suggest a low CO2/O2 atmosphere, e.g., CO2/O2 < 1, on early Mars at the time of deposition. This in turn implies that O2 would not have been derived mainly from CO2 photolysis and may require more effective paths (e.g., H2O photolysis and effective atmospheric escape) for producing O2 in the very early stage of Mars' history.

  13. Clustering XCO2 temporal change to assess CO2 exchanging strength of biosphere-atmosphere with GOSAT observations

    NASA Astrophysics Data System (ADS)

    He, Zhonghua; Lei, Liping; Bie, Nian; Yang, Shaoyuan; Wu, Changjiang; Zeng, Zhao-Cheng

    2017-04-01

    The temporal change of atmospheric carbon dioxide (CO2) concentration, greatly related to the local activities of CO2 uptake and emission, including biospheric exchange and anthropogenic emission, is one of important information for regions identification of carbon source and sink. Satellite observations of CO2 has been used for detecting the change of CO2 concentration for a long time. In this study, we used the grid data of column-averaged CO2 dry air mole fraction (XCO2) with the spatial resolution of 1 degree and the temporal resolution of 3 days from 1 June 2009 to 31 May 2014 over the land area of 30° - 60° N to implement a clustering of temporal changing characteristics for the Greenhouse Gases Observing Satellite (GOSAT) XCO2 retrievals. Grid data is derived using the gap filling method of spatio-temporal geostatistics. The clustering method is one adjusted K-mean for the gap existed time-series data. As a result, types and number of clusters are specified based on the temporal characteristic of XCO2 by using the optimal clustering parameters. The biospheric absorption and surface emission of atmospheric CO2 is discussed through the analysis of the different yearly increase and seasonal amplitude of XCO2 each cluster combined with correlation analysis with vegetation index from the Moderate-resolution Imaging Spectroradiometer (MODIS) and fossil fuel CO2 emission data from Open-source Data Inventory for Anthropogenic CO2 (Odiac). Regions of strong or weak biosphere-atmosphere exchange, or significant disturbance from anthropogenic activities can be identified. In conclusion, gap filled XCO2 from satellite observations can help us to take an analysis of atmospheric CO2, results of the coupled biosphere-atmosphere, by their spatio-temporal characteristics as well as the relationship with the other remote sensing parameters e.g. MODIS related with biospheric photosynthetic or respiration activities.

  14. Increase in the CO2 exchange rate of leaves of Ilex rotunda with elevated atmospheric CO2 concentration in an urban canyon

    NASA Astrophysics Data System (ADS)

    Takagi, M.; Gyokusen, Koichiro; Saito, Akira

    It was found that the atmospheric carbon dioxide (CO2) concentration in an urban canyon in Fukuoka city, Japan during August 1997 was about 30 µmol mol-1 higher than that in the suburbs. When fully exposed to sunlight, in situ the rate of photosynthesis in single leaves of Ilex rotunda planted in the urban canyon was higher when the atmospheric CO2 concentration was elevated. A biochemically based model was able to predict the in situ rate of photosynthesis well. The model also predicted an increase in the daily CO2 exchange rate for leaves in the urban canyon with an increase in atmospheric CO2 concentration. However, in situ such an increase in the daily CO2 exchange rate may be offset by diminished sunlight, a higher air temperature and a lower relative humidity. Thus, the daily CO2 exchange rate predicted using the model based soleley on the environmental conditions prevailing in the urban canyon was lower than that predicted based only on environmental factors found in the suburbs.

  15. Pleistocene atmospheric CO2 change linked to Southern Ocean nutrient utilization

    NASA Astrophysics Data System (ADS)

    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.

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

    NASA Astrophysics Data System (ADS)

    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.

  17. Lidar Observations of Atmospheric CO2 Column During 2014 Summer Flight Campaigns

    NASA Technical Reports Server (NTRS)

    Lin, Bing; Harrison, F. Wallace; Fan, Tai-Fang

    2015-01-01

    Advanced knowledge in atmospheric CO2 is critical in reducing large uncertainties in predictions of the Earth' future climate. Thus, Active Sensing of CO2 Emissions over Nights, Days, and Seasons (ASCENDS) from space was recommended by the U.S. National Research Council to NASA. As part of the preparation for the ASCENDS mission, NASA Langley Research Center (LaRC) and Exelis, Inc. have been collaborating in development and demonstration of the Intensity-Modulated Continuous-Wave (IM-CW) lidar approach for measuring atmospheric CO2 column from space. Airborne laser absorption lidars such as the Multi-Functional Fiber Laser Lidar (MFLL) and ASCENDS CarbonHawk Experiment Simulator (ACES) operating in the 1.57 micron CO2 absorption band have been developed and tested to obtain precise atmospheric CO2 column measurements using integrated path differential absorption technique and to evaluate the potential of the space ASCENDS mission. This presentation reports the results of our lidar atmospheric CO2 column measurements from 2014 summer flight campaign. Analysis shows that for the 27 Aug OCO-2 under flight over northern California forest regions, significant variations of CO2 column approximately 2 ppm) in the lower troposphere have been observed, which may be a challenge for space measurements owing to complicated topographic condition, heterogeneity of surface reflection and difference in vegetation evapotranspiration. Compared to the observed 2011 summer CO2 drawdown (about 8 ppm) over mid-west, 2014 summer drawdown in the same region measured was much weak (approximately 3 ppm). The observed drawdown difference could be the results of the changes in both meteorological states and the phases of growing seasons. Individual lidar CO2 column measurements of 0.1-s integration were within 1-2 ppm of the CO2 estimates obtained from on-board in-situ sensors. For weak surface reflection conditions such as ocean surfaces, the 1- s integrated signal-to-noise ratio (SNR) of

  18. Conversion of CO2 to CO using radio-frequency atmospheric pressure plasmas

    NASA Astrophysics Data System (ADS)

    Foote, Alexander; Dedrick, James; O'Connell, Deborah; North, Michael; Gans, Timo

    2016-09-01

    Low temperature plasmas can be used for the in situ generation of CO, from relatively non-toxic CO2 . CO is very useful in many industrial chemical processes and so, via low temperature plasmas, CO2, a waste product, can be converted into a valuable chemical. The key challenges in using this method, for CO production, are optimising the energy efficiency, maximising the conversion of CO2 into CO and then separating the CO from the other species produced in the plasma. Very high yields of CO, greater than 90%, have been achieved at atmospheric pressure using argon as a carrier gas with admixtures up to 1.5% with energy efficiencies of up to 4%. The plasma generated in continuous and spatially homogeneous and is driven at a frequency of 40.68 MHz. A zero dimensional global model has also been used to simulate the chemical kinetics of the plasma to determine the dominant dissociation processes and is in good agreement with the experimentally determined yields. The model is used to determine how important a role the vibrational states of CO2 are, in a highly collisional plasma, to the production of CO and there can provide insight into how to improve the energy efficiency and suppress unwanted reactions.

  19. The effect of anthropogenic emissions corrections on the seasonal cycle of atmospheric CO2

    NASA Astrophysics Data System (ADS)

    Brooks, B. J.; Hoffman, F. M.; Mills, R. T.; Erickson, D. J.; Blasing, T. J.

    2009-12-01

    A previous study (Erickson et al. 2008) approximated the monthly global emission estimates of anthropogenic CO2 by applying a 2-harmonic Fourier expansion with coefficients as a function of latitude to annual CO2 flux estimates derived from United States data (Blasing et al. 2005) that were extrapolated globally. These monthly anthropogenic CO2 flux estimates were used to model atmospheric concentrations using the NASA GEOS-4 data assimilation system. Local variability in the amplitude of the simulated CO2 seasonal cycle were found to be on the order of 2-6 ppmv. Here we used the same Fourier expansion to seasonally adjust the global annual fossil fuel CO2 emissions from the SRES A2 scenario. For a total of four simulations, both the annual and seasonalized fluxes were advected in two configurations of the NCAR Community Atmosphere Model (CAM) used in the Carbon-Land Model Intercomparison Project (C-LAMP). One configuration used the NCAR Community Land Model (CLM) coupled with the CASA‧ (carbon only) biogeochemistry model and the other used CLM coupled with the CN (coupled carbon and nitrogen cycles) biogeochemistry model. All four simulations were forced with observed sea surface temperatures and sea ice concentrations from the Hadley Centre and a prescribed transient atmospheric CO2 concentration for the radiation and land forcing over the 20th century. The model results exhibit differences in the seasonal cycle of CO2 between the seasonally corrected and uncorrected simulations. Moreover, because of differing energy and water feedbacks between the atmosphere model and the two land biogeochemistry models, features of the CO2 seasonal cycle were different between these two model configurations. This study reinforces previous findings that suggest that regional near-surface atmospheric CO2 concentrations depend strongly on the natural sources and sinks of CO2, but also on the strength of local anthropogenic CO2 emissions and geographic position. This work further

  20. Microbial Assimilation of Atmospheric CO2 to Synthesize Organic Matter in Soils

    NASA Astrophysics Data System (ADS)

    Ge, Tida

    2014-05-01

    Like higher plants, microbial autotrophs possess photosynthetic systems that enable them to fix CO2. Whilst present in large numbers in soils, the capacity for soil microorganisms to fix CO2 and their importance in terrestrial C cycling has not been quantified. To measure the activities of microbial autotrophs in assimilating atmospheric CO2, seven different soils were incubated with 14C labelled CO2 for 80 d, and the 14C-labelled organic C synthesized was determined. The results indicate that the synthesis rates of 14C-lablled organic C ranged from 0.0134 to 0.103 g C m-2 d-1, and were closely related to RubisCO activities and the abundance of cbbL-genes in the soils, indicating that the synthesis could be attributed to soil microbial autotrophs. This finding suggests that microbial assimilation of atmospheric CO2 is an important process in the sequestration and cycling of terrestrial C that, until now, has been largely ignored.

  1. Atmospheric Fossil Fuel CO2 Tracing By 14C In Some Chinese Cities

    NASA Astrophysics Data System (ADS)

    Zhou, W.; Niu, Z.; Zhu, Y., Sr.

    2016-12-01

    CO2 plays an important role in global climate as a primary greenhouse gas in the atmosphere. Moreover, it has been shown that more than 70% of global fossil fuel CO2 (CO2ff) emissions are concentrated in urban areas (Duren and Miller, 2012). Our study focuses on atmospheric CO2ff concentrations in 15 Chinese cities using accelerator mass spectrometer (AMS) to measure 14C. Our objectives are: (1) to document atmospheric CO2ff concentrations in a variety of urban environments, (2) to differentiate the spatial-temporal variations in CO2ff among these cities, and (3) to ascertain the factors that control the observed variations. For about two years (winter 2014 to winter 2016), the CO2ff concentrations we observed from all sites varied from 5.1±4.5 ppm to 65.8±39.0 ppm. We observed that inland cities display much higher CO2ff concentrations and overall temporal variations than coastal cities in winter, and that northern cities have higher CO2ff concentrations than those of southern cities in winter. For inland cities relatively high CO2ff values are observed in winter and low values in summer; while seasonal variations are not distinct in the coastal cities. No significant (p > 0.05) differences in CO2ff values are found between weekdays and weekends as was shown previously in Xi'an (Zhou et al., 2014). Diurnal CO2ff variations are plainly evident, with high values between midnight and 4:00 am, and during morning and afternoon rush hours (Niu et al., 2016). The high CO2ff concentrations in northern inland cities in winter results mainly from the substantial consumption of fossil fuels for heating. The high CO2ff concentrations seen in diurnal measurements result mainly from variations in atmospheric dispersion, and from vehicle emissions related to traffic flows. The inter-annual variations in CO2ff in cities could provide a useful reference for local governments to develop policy around the effect of energy conservation and emission reduction strategies.

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

    PubMed

    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.

  3. Implications of elevated atmospheric CO2 on plant growth and water relations

    USDA-ARS?s Scientific Manuscript database

    Empirical records provide incontestable evidence for the global rise in CO2 concentration in the earth’s atmosphere. Plant growth can be stimulated by elevation of CO2; photosynthesis increases and economic yield is often enhanced. The application of more CO2 can result in less water use. Competitio...

  4. Steady- and non-steady-state carbonate-silicate controls on atmospheric CO2

    USGS Publications Warehouse

    Sundquist, E.T.

    1991-01-01

    Two contrasting hypotheses have recently been proposed for the past long-term relation between atmospheric CO2 and the carbonate-silicate geochemical cycle. One approach (Berner, 1990) suggests that CO2 levels have varied in a manner that has maintained chemical weathering and carbonate sedimentation at a steady state with respect to tectonically controlled decarbonation reactions. A second approach (Raymo et al., 1988), applied specificlly to the late Cenozoic, suggests a decrease in CO2 caused by an uplift-induced increase in chemical weathering, without regard to the rate of decarbonation. According to the steady-state (first) hypothesis, increased weathering and carbonate sedimentation are generally associated with increasing atmospheric CO2, whereas the uplift (second) hypothesis implies decreasing CO2 under the same conditions. An ocean-atmosphere-sediment model has been used to assess the response of atmospheric CO2 and carbonate sedimentation to global perturbations in chemical weathering and decarbonation reactions. Although this assessment is theoretical and cannot yet be related to the geologic record, the model simulations compare steady-state and non-steady-state carbonate-silicate cycle response. The e-fold response time of the 'CO2-weathering' feedback mechanism is between 300 and 400 ka. The response of carbonate sedimentation is much more rapid. These response times provide a measure of the strength of steady-state assumptions, and imply that certain systematic relations are sustained throughout steady-state and non-steady-state scenarios for the carbonate-silicate cycle. The simulations suggest that feedbacks can maintain the system near a steady state, but that non-steady-state effects may contribute to long-term trends. The steady-state and uplift hypotheses are not necessarily incompatible over time scales of a few million years. ?? 1991.

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

    NASA Astrophysics Data System (ADS)

    Oschlies, A.

    2009-04-01

    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. 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. On longer than decadal timescales, a substantial fraction of oceanic carbon uptake induced by natural or purposeful ocean fertilization may not come from the atmosphere but from the terrestrial biosphere.

  6. Measurements of CO2 Column Abundance in the Low Atmosphere Using Ground Based 1.6 μm CO2 DIAL

    NASA Astrophysics Data System (ADS)

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

    2017-12-01

    Changes in atmospheric carbon dioxide (CO2) concentration are believed to produce the largest radiative forcing for the current climate system. Accurate predictions of atmospheric CO2 concentration rely on the knowledge of its sinks and sources, transports, and its variability with time. Although this knowledge is currently unsatisfactory, numerical models use it as a way in simulating CO2 fluxes. Validating and improving the global atmospheric transport model, therefore, requires precise measurement of the CO2 concentration profile. There are two further variations on Lidar: the differential absorption Lidar (DIAL) and the integrated path differential absorption (IPDA) Lidar. DIAL/IPDA are basically for profile/total column measurement, respectively. IPDA is a special case of DIAL and can measure the total column-averaged mixing ratio of trace gases using return signals from the Earth's surface or from thick clouds based on an airborne or a satellite. We have developed a ground based 1.6 μm DIAL to measure vertical CO2 mixing ratio profiles from 0.4 to 2.5 km altitude. The goals of the CO2 DIAL are to produce atmospheric CO2 mixing ratio measurements with much smaller seasonal and diurnal biases from the ground surface. But, in the ground based lidar, return signals from around ground surface are usually suppressed in order to handle the large dynamic range. To receive the return signals as near as possible from ground surface, namely, the field of view (FOV) of the telescope must be wide enough to reduce the blind range of the lidar. While the return signals from the far distance are very weak, to enhance the sensitivity and heighten the detecting distance, the FOV must be narrow enough to suppress the sky background light, especially during the daytime measurements. To solve this problem, we propose a total column measurement method from the ground surface to 0.4 km altitude. Instead of strong signals from thick clouds such as the IPDA, the proposed method uses

  7. Increased soil emissions of potent greenhouse gases under increased atmospheric CO2.

    PubMed

    van Groenigen, Kees Jan; Osenberg, Craig W; Hungate, Bruce A

    2011-07-13

    Increasing concentrations of atmospheric carbon dioxide (CO(2)) can affect biotic and abiotic conditions in soil, such as microbial activity and water content. In turn, these changes might be expected to alter the production and consumption of the important greenhouse gases nitrous oxide (N(2)O) and methane (CH(4)) (refs 2, 3). However, studies on fluxes of N(2)O and CH(4) from soil under increased atmospheric CO(2) have not been quantitatively synthesized. Here we show, using meta-analysis, that increased CO(2) (ranging from 463 to 780 parts per million by volume) stimulates both N(2)O emissions from upland soils and CH(4) emissions from rice paddies and natural wetlands. Because enhanced greenhouse-gas emissions add to the radiative forcing of terrestrial ecosystems, these emissions are expected to negate at least 16.6 per cent of the climate change mitigation potential previously predicted from an increase in the terrestrial carbon sink under increased atmospheric CO(2) concentrations. Our results therefore suggest that the capacity of land ecosystems to slow climate warming has been overestimated. ©2011 Macmillan Publishers Limited. All rights reserved

  8. Recent pause in the growth rate of atmospheric CO2 due to enhanced terrestrial carbon uptake

    PubMed Central

    Keenan, Trevor F; Prentice, I. Colin; Canadell, Josep G; Williams, Christopher A; Wang, Han; Raupach, Michael; Collatz, G. James

    2016-01-01

    Terrestrial ecosystems play a significant role in the global carbon cycle and offset a large fraction of anthropogenic CO2 emissions. The terrestrial carbon sink is increasing, yet the mechanisms responsible for its enhancement, and implications for the growth rate of atmospheric CO2, remain unclear. Here using global carbon budget estimates, ground, atmospheric and satellite observations, and multiple global vegetation models, we report a recent pause in the growth rate of atmospheric CO2, and a decline in the fraction of anthropogenic emissions that remain in the atmosphere, despite increasing anthropogenic emissions. We attribute the observed decline to increases in the terrestrial sink during the past decade, associated with the effects of rising atmospheric CO2 on vegetation and the slowdown in the rate of warming on global respiration. The pause in the atmospheric CO2 growth rate provides further evidence of the roles of CO2 fertilization and warming-induced respiration, and highlights the need to protect both existing carbon stocks and regions, where the sink is growing rapidly. PMID:27824333

  9. Recent pause in the growth rate of atmospheric CO 2 due to enhanced terrestrial carbon uptake

    DOE PAGES

    Keenan, Trevor F.; Prentice, I. Colin; Canadell, Josep G.; ...

    2016-11-08

    Terrestrial ecosystems play a significant role in the global carbon cycle and offset a large fraction of anthropogenic CO 2 emissions. The terrestrial carbon sink is increasing, yet the mechanisms responsible for its enhancement, and implications for the growth rate of atmospheric CO 2, remain unclear. Here using global carbon budget estimates, ground, atmospheric and satellite observations, and multiple global vegetation models, we report a recent pause in the growth rate of atmospheric CO 2, and a decline in the fraction of anthropogenic emissions that remain in the atmosphere, despite increasing anthropogenic emissions. We also attribute the observed decline tomore » increases in the terrestrial sink during the past decade, associated with the effects of rising atmospheric CO 2 on vegetation and the slowdown in the rate of warming on global respiration. Furthermore, the pause in the atmospheric CO 2 growth rate provides further evidence of the roles of CO 2 fertilization and warming-induced respiration, and highlights the need to protect both existing carbon stocks and regions, where the sink is growing rapidly.« less

  10. Recent pause in the growth rate of atmospheric CO 2 due to enhanced terrestrial carbon uptake

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Keenan, Trevor F.; Prentice, I. Colin; Canadell, Josep G.

    Terrestrial ecosystems play a significant role in the global carbon cycle and offset a large fraction of anthropogenic CO 2 emissions. The terrestrial carbon sink is increasing, yet the mechanisms responsible for its enhancement, and implications for the growth rate of atmospheric CO 2, remain unclear. Here using global carbon budget estimates, ground, atmospheric and satellite observations, and multiple global vegetation models, we report a recent pause in the growth rate of atmospheric CO 2, and a decline in the fraction of anthropogenic emissions that remain in the atmosphere, despite increasing anthropogenic emissions. We also attribute the observed decline tomore » increases in the terrestrial sink during the past decade, associated with the effects of rising atmospheric CO 2 on vegetation and the slowdown in the rate of warming on global respiration. Furthermore, the pause in the atmospheric CO 2 growth rate provides further evidence of the roles of CO 2 fertilization and warming-induced respiration, and highlights the need to protect both existing carbon stocks and regions, where the sink is growing rapidly.« less

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

    PubMed

    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 < .05) increases in seasonal peak-to-trough CO 2 amplitude (AMP P -T ) at nine stations, and in trough-to-peak amplitude (AMP T -P ) at eight stations over the last three decades. Most of the stations that recorded increasing amplitudes are in Arctic and boreal regions (>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.

  12. Atmospheric correlation time measurements using coherent CO2 lidar

    NASA Technical Reports Server (NTRS)

    Ancellet, G. M.; Menzies, R. T.

    1986-01-01

    A pulsed TEA-CO2 lidar with coherent detection was used to measure the correlation time of backscatter from an ensemble of atmospheric aerosol particles which are illuminated by the pulsed radiation. The correlation time of the backscatter return signal is important in studies of atmospheric turbulence and its effects on optical propagation and backscatter. If the temporal coherence of the pulse is large enough, then the temporal coherence of the return signal is dominated by the turbulence and shear for a variety of interesting atmospheric conditions. Various techniques for correlation time measurement are discussed and evaluated.

  13. Increasing atmospheric humidity and CO 2 concentration alleviate forest mortality risk

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Liu, Yanlan; Parolari, Anthony J.; Kumar, Mukesh

    Climate-induced forest mortality is being increasingly observed throughout the globe. Alarmingly, it is expected to exacerbate under climate change due to shifting precipitation patterns and rising air temperature. However, the impact of concomitant changes in atmospheric humidity and CO 2 concentration through their influence on stomatal kinetics remains a subject of debate and inquiry. By using a dynamic soil–plant–atmosphere model, mortality risks associated with hydraulic failure and stomatal closure for 13 temperate and tropical forest biomes across the globe are analyzed. The mortality risk is evaluated in response to both individual and combined changes in precipitation amounts and their seasonalmore » distribution, mean air temperature, specific humidity, and atmospheric CO 2 concentration. Model results show that the risk is predicted to significantly increase due to changes in precipitation and air temperature regime for the period 2050–2069. However, this increase may largely get alleviated by concurrent increases in atmospheric specific humidity and CO 2 concentration. The increase in mortality risk is expected to be higher for needleleaf forests than for broadleaf forests, as a result of disparity in hydraulic traits. These findings will further facilitate decisions about intervention and management of different forest types under changing climate.« less

  14. Increasing atmospheric humidity and CO 2 concentration alleviate forest mortality risk

    DOE PAGES

    Liu, Yanlan; Parolari, Anthony J.; Kumar, Mukesh; ...

    2017-08-28

    Climate-induced forest mortality is being increasingly observed throughout the globe. Alarmingly, it is expected to exacerbate under climate change due to shifting precipitation patterns and rising air temperature. However, the impact of concomitant changes in atmospheric humidity and CO 2 concentration through their influence on stomatal kinetics remains a subject of debate and inquiry. By using a dynamic soil–plant–atmosphere model, mortality risks associated with hydraulic failure and stomatal closure for 13 temperate and tropical forest biomes across the globe are analyzed. The mortality risk is evaluated in response to both individual and combined changes in precipitation amounts and their seasonalmore » distribution, mean air temperature, specific humidity, and atmospheric CO 2 concentration. Model results show that the risk is predicted to significantly increase due to changes in precipitation and air temperature regime for the period 2050–2069. However, this increase may largely get alleviated by concurrent increases in atmospheric specific humidity and CO 2 concentration. The increase in mortality risk is expected to be higher for needleleaf forests than for broadleaf forests, as a result of disparity in hydraulic traits. These findings will further facilitate decisions about intervention and management of different forest types under changing climate.« less

  15. Interpreting OCO-2 Constrained CO2 Surface Flux Estimates Through the Lens of Atmospheric Transport Uncertainty.

    NASA Astrophysics Data System (ADS)

    Schuh, A. E.; Jacobson, A. R.; Basu, S.; Weir, B.; Baker, D. F.; Bowman, K. W.; Chevallier, F.; Crowell, S.; Deng, F.; Denning, S.; Feng, L.; Liu, J.

    2017-12-01

    The orbiting carbon observatory (OCO-2) was launched in July 2014 and has collected three years of column mean CO2 (XCO2) data. The OCO-2 model inter-comparison project (MIP) was formed to provide a means of analysis of results from many different atmospheric inversion modeling systems. Certain facets of the inversion systems, such as observations and fossil fuel CO2 fluxes were standardized to remove first order sources of difference between the systems. Nevertheless, large variations amongst the flux results from the systems still exist. In this presentation, we explore one dimension of this uncertainty, the impact of different atmospheric transport fields, i.e. wind speeds and directions. Early results illustrate a large systematic difference between two classes of atmospheric transport, arising from winds in the parent GEOS-DAS (NASA-GMAO) and ERA-Interim (ECMWF) data assimilation models. We explore these differences and their effect on inversion-based estimates of surface CO2 flux by using a combination of simplified inversion techniques as well as the full OCO-2 MIP suite of CO2 flux estimates.

  16. The effect of anthropogenic emissions corrections on the seasonal cycle of atmospheric CO2

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Hoffman, Forrest M; Erickson III, David J; Blasing, T J

    A previous study (Erickson et al. 2008) approximated the monthly global emission estimates of anthropogenic CO{sub 2} by applying a 2-harmonic Fourier expansion with coefficients as a function of latitude to annual CO{sub 2} flux estimates derived from United States data (Blasing et al. 2005) that were extrapolated globally. These monthly anthropogenic CO{sub 2} flux estimates were used to model atmospheric concentrations using the NASA GEOS-4 data assimilation system. Local variability in the amplitude of the simulated CO{sub 2} seasonal cycle were found to be on the order of 2-6 ppmv. Here we used the same Fourier expansion to seasonallymore » adjust the global annual fossil fuel CO{sub 2} emissions from the SRES A2 scenario. For a total of four simulations, both the annual and seasonalized fluxes were advected in two configurations of the NCAR Community Atmosphere Model (CAM) used in the Carbon-Land Model Intercomparison Project (C-LAMP). One configuration used the NCAR Community Land Model (CLM) coupled with the CASA (carbon only) biogeochemistry model and the other used CLM coupled with the CN (coupled carbon and nitrogen cycles) biogeochemistry model. All four simulations were forced with observed sea surface temperatures and sea ice concentrations from the Hadley Centre and a prescribed transient atmospheric CO{sub 2} concentration for the radiation and land forcing over the 20th century. The model results exhibit differences in the seasonal cycle of CO{sub 2} between the seasonally corrected and uncorrected simulations. Moreover, because of differing energy and water feedbacks between the atmosphere model and the two land biogeochemistry models, features of the CO{sub 2} seasonal cycle were different between these two model configurations. This study reinforces previous findings that suggest that regional near-surface atmospheric CO{sub 2} concentrations depend strongly on the natural sources and sinks of CO{sub 2}, but also on the strength of local

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

    NASA Astrophysics Data System (ADS)

    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

  18. Shock-induced CO2 loss from CaCO3: Implications for early planetary atmospheres

    NASA Technical Reports Server (NTRS)

    Lange, M. A.; Ahrens, T. J.

    1984-01-01

    Recovered samples from shock recovery experiments on single crystal calcite were subjected to thermogravimetric analysis to determine the amount of post-shock CO2, the decarbonization interval and the activation energy, for the removal of remaining CO2 in shock-loaded calcite. Comparison of post-shock CO2 with that initially present determines shock-induced CO2 loss as a function of shock pressure. Incipient to complete CO2 loss occurs over a pressure range of approximately 10 to approximately 70 GPa. Optical and scanning electron microscopy reveal structural changes, which are related to the shock-loading. The occurrence of dark, diffuse areas, which can be resolved as highly vesicular areas as observed with a scanning electron microscope are interpreted as representing quenched partial melts, into which shock-released CO2 was injected. The experimental results are used to constrain models of shock-produced, primary CO2 atmospheres on the accreting terrestrial planets.

  19. Space Based Measurements for Atmospheric Carbon Dioxide: a New Tool for Monitoring Our Environment

    NASA Technical Reports Server (NTRS)

    Crisp, David

    2015-01-01

    Fossil fuel combustion, deforestation, and other human activities are now adding almost 40 billion tons of carbon dioxide (CO2) to the atmosphere each year. Interestingly, as these emissions have increased over time, natural "sinks" in land biosphere and oceans have absorbed roughly half of this CO2, reducing the rate of atmospheric buildup by a half. Measurements of the increasing acidity (pH) of seawater indicate that the ocean absorbs one quarter of this CO2. Another quarter is apparently being absorbed by the land biosphere, but the identity and location of these natural land CO2 "sinks" are still unknown. The existing ground-based greenhouse gas monitoring network provides an accurate record of the atmospheric buildup, but still does not have the spatial resolution or coverage needed to identify or quantify CO2 sources and sinks.

  20. Scrutinizing the carbon cycle and CO2 residence time in the atmosphere

    NASA Astrophysics Data System (ADS)

    Harde, Hermann

    2017-05-01

    Climate scientists presume that the carbon cycle has come out of balance due to the increasing anthropogenic emissions from fossil fuel combustion and land use change. This is made responsible for the rapidly increasing atmospheric CO2 concentrations over recent years, and it is estimated that the removal of the additional emissions from the atmosphere will take a few hundred thousand years. Since this goes along with an increasing greenhouse effect and a further global warming, a better understanding of the carbon cycle is of great importance for all future climate change predictions. We have critically scrutinized this cycle and present an alternative concept, for which the uptake of CO2 by natural sinks scales proportional with the CO2 concentration. In addition, we consider temperature dependent natural emission and absorption rates, by which the paleoclimatic CO2 variations and the actual CO2 growth rate can well be explained. The anthropogenic contribution to the actual CO2 concentration is found to be 4.3%, its fraction to the CO2 increase over the Industrial Era is 15% and the average residence time 4 years.

  1. Bench-Scale Process for Low-Cost Carbon Dioxide (CO2) Capture Using a Phase-Changing Absorbent

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Westendorf, Tiffany; Caraher, Joel; Chen, Wei

    2015-03-31

    The objective of this project is to design and build a bench-scale process for a novel phase-changing aminosilicone-based CO2-capture solvent. The project will establish scalability and technical and economic feasibility of using a phase-changing CO2-capture absorbent for post-combustion capture of CO2 from coal-fired power plants with 90% capture efficiency and 95% CO2 purity at a cost of $40/tonne of CO2 captured by 2025 and a cost of <$10/tonne of CO2 captured by 2035. In the first budget period of this project, the bench-scale phase-changing CO2 capture process was designed using data and operating experience generated under a previous project (ARPA-emore » project DE-AR0000084). Sizing and specification of all major unit operations was completed, including detailed process and instrumentation diagrams. The system was designed to operate over a wide range of operating conditions to allow for exploration of the effect of process variables on CO2 capture performance.« less

  2. Comparing Amazon Basin CO2 fluxes from an atmospheric inversion with TRENDY biosphere models

    NASA Astrophysics Data System (ADS)

    Diffenbaugh, N. S.; Alden, C. B.; Harper, A. B.; Ahlström, A.; Touma, D. E.; Miller, J. B.; Gatti, L. V.; Gloor, M.

    2015-12-01

    Net exchange of carbon dioxide (CO2) between the atmosphere and the terrestrial biosphere is sensitive to environmental conditions, including extreme heat and drought. Of particular importance for local and global carbon balance and climate are the expansive tracts of tropical rainforest located in the Amazon Basin. Because of the Basin's size and ecological heterogeneity, net biosphere CO2 exchange with the atmosphere remains largely un-constrained. In particular, the response of net CO2 exchange to changes in environmental conditions such as temperature and precipitation are not yet well known. However, proper representation of these relationships in biosphere models is a necessary constraint for accurately modeling future climate and climate-carbon cycle feedbacks. In an effort to compare biosphere response to climate across different biosphere models, the TRENDY model intercomparison project coordinated the simulation of CO2 fluxes between the biosphere and atmosphere, in response to historical climate forcing, by 9 different Dynamic Global Vegetation Models. We examine the TRENDY model results in the Amazon Basin, and compare this "bottom-up" method with fluxes derived from a "top-down" approach to estimating net CO2 fluxes, obtained through atmospheric inverse modeling using CO2 measurements sampled by aircraft above the basin. We compare the "bottom-up" and "top-down" fluxes in 5 sub-regions of the Amazon basin on a monthly basis for 2010-2012. Our results show important periods of agreement between some models in the TRENDY suite and atmospheric inverse model results, notably the simulation of increased biosphere CO2 loss during wet season heat in the Central Amazon. During the dry season, however, model ability to simulate observed response of net CO2 exchange to drought was varied, with few models able to reproduce the "top-down" inversion flux signals. Our results highlight the value of atmospheric trace gas observations for helping to narrow the

  3. Los Angeles megacity: a high-resolution land–atmosphere modelling system for urban CO 2 emissions

    DOE PAGES

    Feng, Sha; Lauvaux, Thomas; Newman, Sally; ...

    2016-07-22

    Megacities are major sources of anthropogenic fossil fuel CO 2 (FFCO 2) emissions. The spatial extents of these large urban systems cover areas of 10 000 km 2 or more with complex topography and changing landscapes. We present a high-resolution land–atmosphere modelling system for urban CO 2 emissions over the Los Angeles (LA) megacity area. The Weather Research and Forecasting (WRF)-Chem model was coupled to a very high-resolution FFCO 2 emission product, Hestia-LA, to simulate atmospheric CO 2 concentrations across the LA megacity at spatial resolutions as fine as ~1 km. We evaluated multiple WRF configurations, selecting one that minimizedmore » 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 CO 2 emission products to evaluate the impact of the spatial resolution of the CO 2 emission products and the meteorological transport model on the representation of spatiotemporal variability in simulated atmospheric CO 2 concentrations. We find that high spatial resolution in the fossil fuel CO 2 emissions is more important than in the atmospheric model to capture CO 2 concentration variability across the LA megacity. Finally, we present a novel approach that employs simultaneous correlations of the simulated atmospheric CO 2 fields to qualitatively evaluate the greenhouse gas measurement network over the LA megacity. Spatial correlations in the atmospheric CO 2 fields reflect the coverage of individual

  4. Los Angeles megacity: a high-resolution land–atmosphere modelling system for urban CO 2 emissions

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Feng, Sha; Lauvaux, Thomas; Newman, Sally

    Megacities are major sources of anthropogenic fossil fuel CO 2 (FFCO 2) emissions. The spatial extents of these large urban systems cover areas of 10 000 km 2 or more with complex topography and changing landscapes. We present a high-resolution land–atmosphere modelling system for urban CO 2 emissions over the Los Angeles (LA) megacity area. The Weather Research and Forecasting (WRF)-Chem model was coupled to a very high-resolution FFCO 2 emission product, Hestia-LA, to simulate atmospheric CO 2 concentrations across the LA megacity at spatial resolutions as fine as ~1 km. We evaluated multiple WRF configurations, selecting one that minimizedmore » 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 CO 2 emission products to evaluate the impact of the spatial resolution of the CO 2 emission products and the meteorological transport model on the representation of spatiotemporal variability in simulated atmospheric CO 2 concentrations. We find that high spatial resolution in the fossil fuel CO 2 emissions is more important than in the atmospheric model to capture CO 2 concentration variability across the LA megacity. Finally, we present a novel approach that employs simultaneous correlations of the simulated atmospheric CO 2 fields to qualitatively evaluate the greenhouse gas measurement network over the LA megacity. Spatial correlations in the atmospheric CO 2 fields reflect the coverage of individual

  5. Porous CNTs/Co Composite Derived from Zeolitic Imidazolate Framework: A Lightweight, Ultrathin, and Highly Efficient Electromagnetic Wave Absorber.

    PubMed

    Yin, Yichao; Liu, Xiaofang; Wei, Xiaojun; Yu, Ronghai; Shui, Jianglan

    2016-12-21

    Porous carbon nanotubes/cobalt nanoparticles (CNTs/Co) composite with dodecahedron morphology was synthesized by in situ pyrolysis of the Co-based zeolitic imidazolate framework in a reducing atmosphere. The morphology and microstructure of the composite can be well tuned by controlling the pyrolysis conditions. At lower pyrolysis temperature, the CNTs/Co composite is composed of well-dispersed Co nanoparticles and short CNT clusters with low graphitic degree. The increase of pyrolysis temperature/time promotes the growth and graphitization of CNTs and leads to the aggregation of Co nanoparticles. The optimized CNTs/Co composite exhibits strong dielectric and magnetic losses as well as a good impedance matching property. Interestingly, the CNTs/Co composite displays extremely strong electromagnetic wave absorption with a maximum reflection loss of -60.4 dB. More importantly, the matching thickness of the absorber is as thin as 1.81 mm, and the filler loading of composite in the matrix is only 20 wt %. The highly efficient absorption is closely related to the well-designed structure and the synergistic effect between CNTs and Co nanoparticles. The excellent absorbing performance together with lightweight and ultrathin thickness endows the CNTs/Co composite with the potential for application in the electromagnetic wave absorbing field.

  6. Plate tectonic controls on atmospheric CO2 levels since the Triassic.

    PubMed

    Van Der Meer, Douwe G; Zeebe, Richard E; van Hinsbergen, Douwe J J; Sluijs, Appy; Spakman, Wim; Torsvik, Trond H

    2014-03-25

    Climate trends on timescales of 10s to 100s of millions of years are controlled by changes in solar luminosity, continent distribution, and atmosphere composition. Plate tectonics affect geography, but also atmosphere composition through volcanic degassing of CO2 at subduction zones and midocean ridges. So far, such degassing estimates were based on reconstructions of ocean floor production for the last 150 My and indirectly, through sea level inversion before 150 My. Here we quantitatively estimate CO2 degassing by reconstructing lithosphere subduction evolution, using recent advances in combining global plate reconstructions and present-day structure of the mantle. First, we estimate that since the Triassic (250-200 My) until the present, the total paleosubduction-zone length reached up to ∼200% of the present-day value. Comparing our subduction-zone lengths with previously reconstructed ocean-crust production rates over the past 140 My suggests average global subduction rates have been constant, ∼6 cm/y: Higher ocean-crust production is associated with longer total subduction length. We compute a strontium isotope record based on subduction-zone length, which agrees well with geological records supporting the validity of our approach: The total subduction-zone length is proportional to the summed arc and ridge volcanic CO2 production and thereby to global volcanic degassing at plate boundaries. We therefore use our degassing curve as input for the GEOCARBSULF model to estimate atmospheric CO2 levels since the Triassic. Our calculated CO2 levels for the mid Mesozoic differ from previous modeling results and are more consistent with available proxy data.

  7. Plate tectonic controls on atmospheric CO2 levels since the Triassic

    PubMed Central

    Van Der Meer, Douwe G.; Zeebe, Richard E.; van Hinsbergen, Douwe J. J.; Sluijs, Appy; Spakman, Wim; Torsvik, Trond H.

    2014-01-01

    Climate trends on timescales of 10s to 100s of millions of years are controlled by changes in solar luminosity, continent distribution, and atmosphere composition. Plate tectonics affect geography, but also atmosphere composition through volcanic degassing of CO2 at subduction zones and midocean ridges. So far, such degassing estimates were based on reconstructions of ocean floor production for the last 150 My and indirectly, through sea level inversion before 150 My. Here we quantitatively estimate CO2 degassing by reconstructing lithosphere subduction evolution, using recent advances in combining global plate reconstructions and present-day structure of the mantle. First, we estimate that since the Triassic (250–200 My) until the present, the total paleosubduction-zone length reached up to ∼200% of the present-day value. Comparing our subduction-zone lengths with previously reconstructed ocean-crust production rates over the past 140 My suggests average global subduction rates have been constant, ∼6 cm/y: Higher ocean-crust production is associated with longer total subduction length. We compute a strontium isotope record based on subduction-zone length, which agrees well with geological records supporting the validity of our approach: The total subduction-zone length is proportional to the summed arc and ridge volcanic CO2 production and thereby to global volcanic degassing at plate boundaries. We therefore use our degassing curve as input for the GEOCARBSULF model to estimate atmospheric CO2 levels since the Triassic. Our calculated CO2 levels for the mid Mesozoic differ from previous modeling results and are more consistent with available proxy data. PMID:24616495

  8. Intensity-Modulated Continuous-Wave Lidar at 1.57 Micrometer for Atmospheric CO2 Measurements

    NASA Technical Reports Server (NTRS)

    Lin, Bing; Ismail, Syed; Browell, Edward; Meadows, Byron; Nehrir, Amin; Harrison, Wallace F.; Dobler, Jeremy; Obland, Michael

    2014-01-01

    Understanding the earth's carbon cycle is essential for diagnosing current and predicting future climates, which requires precise global measurements of atmospheric CO2 through space missions. The Active Sensing of CO2 Emissions over Nights, Days, and Seasons (ASCENDS) space mission will provide accurate global atmospheric CO2 measurements to meet carbon science requirements. The joint team of NASA Langley Research Center and ITT Exelis, Inc proposes to use the intensity-modulated, continuous-wave (IM-CW) lidar approach for the ASCENDS mission. Prototype instruments have been developed and used to demonstrate the power, signal-to-noise ratio, precision and accuracy, spectral purity, and stability of the measurement and the instrument needed for atmospheric CO2 observations from space. The ranging capability from laser platform to ground surfaces or intermediate backscatter layers is achieved by transmitted range-encoded IM laser signals. Based on the prototype instruments and current lidar technologies, space lidar systems and their CO2 column measurements are analyzed. These studies exhibit a great potential of using IM-CW lidar system for the active space CO2 mission ASCENDS.

  9. Drivers of multi-century trends in the atmospheric CO2 mean annual cycle in a prognostic ESM

    NASA Astrophysics Data System (ADS)

    Liptak, Jessica; Keppel-Aleks, Gretchen; Lindsay, Keith

    2017-03-01

    The amplitude of the mean annual cycle of atmospheric CO2 is a diagnostic of seasonal surface-atmosphere carbon exchange. Atmospheric observations show that this quantity has increased over most of the Northern Hemisphere (NH) extratropics during the last 3 decades, likely from a combination of enhanced atmospheric CO2, climate change, and anthropogenic land use change. Accurate climate prediction requires accounting for long-term interactions between the environment and carbon cycling; thus, analysis of the evolution of the mean annual cycle in a fully prognostic Earth system model may provide insight into the multi-decadal influence of environmental change on the carbon cycle. We analyzed the evolution of the mean annual cycle in atmospheric CO2 simulated by the Community Earth System Model (CESM) from 1950 to 2300 under three scenarios designed to separate the effects of climate change, atmospheric CO2 fertilization, and land use change. The NH CO2 seasonal amplitude increase in the CESM mainly reflected enhanced primary productivity during the growing season due to climate change and the combined effects of CO2 fertilization and nitrogen deposition over the mid- and high latitudes. However, the simulations revealed shifts in key climate drivers of the atmospheric CO2 seasonality that were not apparent before 2100. CO2 fertilization and nitrogen deposition in boreal and temperate ecosystems were the largest contributors to mean annual cycle amplification over the midlatitudes for the duration of the simulation (1950-2300). Climate change from boreal ecosystems was the main driver of Arctic CO2 annual cycle amplification between 1950 and 2100, but CO2 fertilization had a stronger effect on the Arctic CO2 annual cycle amplitude during 2100-2300. Prior to 2100, the NH CO2 annual cycle amplitude increased in conjunction with an increase in the NH land carbon sink. However, these trends decoupled after 2100, underscoring that an increasing atmospheric CO2 annual

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

    NASA Technical Reports Server (NTRS)

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

    2015-01-01

    One of the most compelling features of the Gale landing site is its age. Based on crater counts, the formation of Gale crater is dated to be near the beginning of the Hesperian near the pivotal Hesperian/Noachian transition. This is a time period on Mars that is linked to increased fluvial activity through valley network formation and also marks a transition from higher erosion rates/clay mineral formation to lower erosion rates with mineralogies dominated by sulfate minerals. Results from the Curiosity mission have shown extensive evidence for fluvial activity within the crater suggesting that sediments on the floor of the crater and even sediments making up Mt. Sharp itself were the result of longstanding activity of liquid water. Warm/wet conditions on early Mars are likely due to a thicker atmosphere and increased abundance of greenhouse gases including the main component of the atmosphere, CO2. Carbon dioxide is minor component of the Earth's atmosphere yet plays a major role in surface water chemistry, weathering, and formation of secondary minerals. An ancient martian atmosphere was likely dominated by CO2 and any waters in equilibrium with this atmosphere would have different chemical characteristics. Studies have noted that high partial pressures of CO2 would result in increased carbonic acid formation and lowering of the pH so that carbonate minerals are not stable. However, if there were a dense CO2 atmosphere present at the Hesperian/Noachian transition, it would have to be stored in a carbon reservoir on the surface or lost to space. The Mt. Sharp sediments are potentially one of the best places on Mars to investigate these CO2 reservoirs as they are proposed to have formed in the early Hesperian, from an alkaline lake, and record the transition to an aeolian dominated regime near the top of the sequence. The total amount of CO2 in the Gale crater soils and sediments is significant but lower than expected if a thick atmosphere was present at the

  11. RISING ATMOSPHERIC CO2 AND CARBON SEQUESTRATION IN FORESTS

    EPA Science Inventory

    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...

  12. North America's net terrestrial CO 2 exchange with the atmosphere 1990–2009

    DOE PAGES

    King, Anthony W.; Andres, Robert; Davis, Kenneth J.; ...

    2015-01-21

    Scientific understanding of the global carbon cycle is required for developing national and international policy to mitigate fossil fuel CO 2 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 CO 2 exchange for North America (Canada, United States, and Mexico) over the period 1990–2009. Only CO 2 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 thatmore » the North American land surface was a sink for atmospheric CO 2, 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 CO 2 in the atmosphere in the late 20th and early 21st century. With North America's mean annual fossil fuel CO 2 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 CO 2 sink, the continent's source : sink ratio for this time period was 1720:472, or

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

    USGS Publications Warehouse

    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

  14. North America's net terrestrial CO 2 exchange with the atmosphere 1990–2009

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    King, Anthony W.; Andres, Robert; Davis, Kenneth J.

    Scientific understanding of the global carbon cycle is required for developing national and international policy to mitigate fossil fuel CO 2 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 CO 2 exchange for North America (Canada, United States, and Mexico) over the period 1990–2009. Only CO 2 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 thatmore » the North American land surface was a sink for atmospheric CO 2, 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 CO 2 in the atmosphere in the late 20th and early 21st century. With North America's mean annual fossil fuel CO 2 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 CO 2 sink, the continent's source : sink ratio for this time period was 1720:472, or

  15. Modification of land-atmosphere interactions by CO2 effects

    NASA Astrophysics Data System (ADS)

    Lemordant, Leo; Gentine, Pierre

    2017-04-01

    Plant stomata couple the energy, water and carbon cycles. Increased CO2 modifies the seasonality of the water cycle through stomatal regulation and increased leaf area. As a result, the water saved during the growing season through higher water use efficiency mitigates summer dryness and the impact of potential heat waves. Land-atmosphere interactions and CO2 fertilization together synergistically contribute to increased summer transpiration. This, in turn, alters the surface energy budget and decreases sensible heat flux, mitigating air temperature rise. Accurate representation of the response to higher CO2 levels, and of the coupling between the carbon and water cycles are therefore critical to forecasting seasonal climate, water cycle dynamics and to enhance the accuracy of extreme event prediction under future climate.

  16. Double-Pulsed 2-Micrometer Lidar Validation for Atmospheric CO2 Measurements

    NASA Technical Reports Server (NTRS)

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

    2015-01-01

    A double-pulsed, 2-micron Integrated Path Differential Absorption (IPDA) lidar instrument for atmospheric carbon dioxide (CO2) measurements is successfully developed at NASA Langley Research Center (LaRC). Based on direct detection technique, the instrument can be operated on ground or onboard a small aircraft. Key features of this compact, rugged and reliable IPDA lidar includes high transmitted laser energy, wavelength tuning, switching and locking, and sensitive detection. As a proof of concept, the IPDA ground and airborne CO2 measurement and validation will be presented. IPDA lidar CO2 measurements ground validation were conducted at NASA LaRC using hard targets and a calibrated in-situ sensor. Airborne validation, conducted onboard the NASA B-200 aircraft, included CO2 plum detection from power stations incinerators, comparison to in-flight CO2 in-situ sensor and comparison to air sampling at different altitude conducted by NOAA at the same site. Airborne measurements, spanning for 20 hours, were obtained from different target conditions. Ground targets included soil, vegetation, sand, snow and ocean. In addition, cloud slicing was examined over the ocean. These flight validations were conducted at different altitudes, up to 7 km, with different wavelength controlled weighing functions. CO2 measurement results agree with modeling conducted through the different sensors, as will be discussed.

  17. CO2-dominated Atmosphere in Equilibrium with NH3-H2O Ocean: Application to Early Titan and Ocean Planets

    NASA Astrophysics Data System (ADS)

    Marounina, N.; Grasset, O.; Tobie, G.; Carpy, S.

    2015-12-01

    During the accretion of Titan, impact heating may have been sufficient to allow the global melting of water ice (Monteux et al. 2014) and the release of volatile compounds, with CO2 and NH3 as main constituents (Tobie et al. 2012). Thus, on primitive Titan, it is thought that a massive atmosphere was in contact with a global water ocean. Similar configurations may occur on temperate water-rich planets called ocean planets (Léger et al. 2004, Kitzmann et al. 2015).Due to its rather low solubility in liquid water, carbon dioxide is expected to be one of the major components in the atmosphere. The atmospheric amount of CO2 is a key parameter for assessing the thermal evolution of the planetary surface because of its strong greenhouse effect. However, ammonia significantly affects the solubility of CO2 in water and hence the atmosphere-ocean thermo-chemical equilibrium. For primitive Titan, estimating the mass, temperature and composition of the primitive atmosphere is important to determine mechanisms that led to the present-day N2-CH4 dominated atmosphere. Similarly, for ocean planets, the influence of ammonia on the atmospheric abundance in CO2 has consequences for the definition of the habitable zone.To investigate the atmospheric composition of the water-rich worlds for a wide range of initial compositions, we have developed a vapor-liquid equilibrium model of the NH3-CO2-H2O system, where we account for the non-ideal comportment of both vapor and liquid phases and the ion speciation of volatiles dissolved in the aqueous phase. We show that adding NH3 to the CO2-H2O binary system induces an efficient absorption of the CO2 in the liquid phase and thus a lower CO2 partial pressure in the vapor phase. Indeed, the CO2 partial pressure remains low for the CO2/NH3 ratio of liquid concentrations lower than 0.5.Assuming various initial compositions of Titan's global water ocean, we explore the thermal and compositional evolution of a massive primitive atmosphere using

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

    NASA Astrophysics Data System (ADS)

    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.

  19. Recharge of the early atmosphere of Mars by impact-induced release of CO2

    USGS Publications Warehouse

    Carr, Michael H.

    1989-01-01

    Channels on the Martian surface suggest that Mars had an early, relatively thick atmosphere. If the atmosphere was thick enough for water to be stable at the surface, CO2 in the atmosphere would have been fixed as carbonates on a relatively short time scale, previously estimated to be 1 bar every 107 years. This loss must have been offset by some replenishment mechanism to account for the numerous valley networks in the oldest surviving terrains. Impacts could have released CO2 into the atmosphere by burial, by shock-induced release during impact events, and by addition of carbon to Mars from the impacting bolides. Depending on the relationship between the transient cavity diameter and the diameter of the resulting crater, burial rates as a result of impact gardening at the end of heavy bombardment are estimated to range from 20 to 45 m/106 years, on the assumption that cratering rates in Mars were similar to those of the Nectarian Period on the Moon. At these rates 0.1-0.2 bar of CO2 could have been released every 107 years as a result of burial to depths where dissociation temperatures of carbonates were reached. Modeling of large impacts suggests that an additional 0.01 to 0.02 bar of CO2 could have been released every 107 years during the actual impacts. In the unlikely event that all the impacting material was composed of carbonaceous chondrites, a further 0.3 bar of CO2 could have been added to the atmosphere every 107 years by oxidation of meteoritic carbon. Even when supplemented by the volcanically induced release of CO2, these release rates are barely sufficient to sustain an early atmosphere if water were continuously present at the surface. The results suggest that water may have been only intermittently present on the surface early in the planet's history.

  20. Implications of ``peak oil'' for atmospheric CO2 and climate

    NASA Astrophysics Data System (ADS)

    Kharecha, Pushker A.; Hansen, James E.

    2008-09-01

    Unconstrained CO2 emission from fossil fuel burning has been the dominant cause of observed anthropogenic global warming. The amounts of "proven" and potential fossil fuel reserves are uncertain and debated. Regardless of the true values, society has flexibility in the degree to which it chooses to exploit these reserves, especially unconventional fossil fuels and those located in extreme or pristine environments. If conventional oil production peaks within the next few decades, it may have a large effect on future atmospheric CO2 and climate change, depending upon subsequent energy choices. Assuming that proven oil and gas reserves do not greatly exceed estimates of the Energy Information Administration, and recent trends are toward lower estimates, we show that it is feasible to keep atmospheric CO2 from exceeding about 450 ppm by 2100, provided that emissions from coal, unconventional fossil fuels, and land use are constrained. Coal-fired power plants without sequestration must be phased out before midcentury to achieve this CO2 limit. It is also important to "stretch" conventional oil reserves via energy conservation and efficiency, thus averting strong pressures to extract liquid fuels from coal or unconventional fossil fuels while clean technologies are being developed for the era "beyond fossil fuels". We argue that a rising price on carbon emissions is needed to discourage conversion of the vast fossil resources into usable reserves, and to keep CO2 beneath the 450 ppm ceiling.

  1. Development of a Micro Pulsed Lidar and a Singly-Resonant Optical Parametric Oscillator for CO2 Dial for Use in Atmospheric Studies

    NASA Astrophysics Data System (ADS)

    Chantjaroen, Chat

    According to the Fifth Assessment Report (AR5) from the Intergovernmental Panel on Climate Change (IPCC), aerosols and CO2 are the largest contributors to anthropogenic radiative forcing--net negative for aerosols and positive for CO2. This relates to the amount of impact that aerosols and CO2 can have on our atmosphere and climate system. CO2 is the predominant greenhouse gas in the atmosphere and causes great impacts on our climate system. Recent studies show that a less well known atmospheric component--aerosols, which are solid particles or liquid droplets suspended in air, can cause great impact on our climate system too. They can affect our climate directly by absorbing and scattering sunlight to warm or cool our climate. They can also affect our climate indirectly by affecting cloud microphysical properties. Typically sulfate aerosols or sea salts act as condensation nuclei for clouds to form. Clouds are estimated to shade about 60% of the earth at any given time. They are preventing much of the sunlight from reaching the earth's surface and are helping with the flow of the global water cycle. These are what permit lifeforms on earth. In the IPCC report, both aerosols and CO2 also have the largest uncertainties and aerosols remains at a low level of scientific understanding. These indicate the need of more accurate measurements and that new technologies and instruments needs to be developed. This dissertation focuses on the development of two instruments--a scannable Micro-Pulsed Lidar (MPL) for atmospheric aerosol measurements and an Optical Parametric Oscillator (OPO) for use as a transmitter in a Differential Absorption Lidar (DIAL) for atmospheric CO2 measurements. The MPL demonstrates successful measurements of aerosols. It provides the total aerosol optical depth (AOD) and aerosol lidar ratio (Sa) that agree well with an instrument used by the Aerosol Robotic Network (AERONET). It also successfully provides range-resolved information about aerosols

  2. Land Use Effects on Atmospheric C-13 Imply a Sizable Terrestrial CO2 Sink in Tropical Latitudes

    NASA Technical Reports Server (NTRS)

    Townsend, Alan R.; Asner, Gregory P.; Tans, Pieter P.; White, James W. C.

    2000-01-01

    Records of atmospheric CO2 and 13-CO2, can be used to distinguish terrestrial vs. oceanic exchanges of CO2 with the atmosphere. However, this approach has proven difficult in the tropics, partly due to extensive land conversion from C-3 to C-4 vegetation. We estimated the effects of such conversion on biosphere-atmosphere C-13 exchange for 1991 through 1999, and then explored how this 'land-use disequilibrium' altered the partitioning of net atmospheric CO2 exchanges between ocean and land using NOAA-CMDL data and a 2D, zonally averaged atmospheric transport model. Our results show sizable CO2 uptake in C-3-dominated tropical regions in seven of the nine years; 1997 and 1998, which included a strong ENSO event, are near neutral. Since these fluxes include any deforestation source, our findings imply either that such sources are smaller than previously estimated, and/or the existence of a large terrestrial CO2 sink in equatorial latitudes.

  3. Radiocarbon observations in atmospheric CO2: determining fossil fuel CO2 over Europe using Jungfraujoch observations as background.

    PubMed

    Levin, Ingeborg; Hammer, Samuel; Kromer, Bernd; Meinhardt, Frank

    2008-03-01

    Monthly mean 14CO2 observations at two regional stations in Germany (Schauinsland observatory, Black Forest, and Heidelberg, upper Rhine valley) are compared with free tropospheric background measurements at the High Alpine Research Station Jungfraujoch (Swiss Alps) to estimate the regional fossil fuel CO2 surplus at the regional stations. The long-term mean fossil fuel CO2 surplus at Schauinsland is 1.31+/-0.09 ppm while it is 10.96+/-0.20 ppm in Heidelberg. No significant trend is observed at both sites over the last 20 years. Strong seasonal variations of the fossil fuel CO2 offsets indicate a strong seasonality of emissions but also of atmospheric dilution of ground level emissions by vertical mixing.

  4. An atmospheric pCO2 reconstruction across the Cretaceous-Tertiary boundary from leaf megafossils

    PubMed Central

    Beerling, D. J.; Lomax, B. H.; Royer, D. L.; Upchurch, G. R.; Kump, L. R.

    2002-01-01

    The end-Cretaceous mass extinctions, 65 million years ago, profoundly influenced the course of biotic evolution. These extinctions coincided with a major extraterrestrial impact event and massive volcanism in India. Determining the relative importance of each event as a driver of environmental and biotic change across the Cretaceous-Tertiary boundary (KTB) crucially depends on constraining the mass of CO2 injected into the atmospheric carbon reservoir. Using the inverse relationship between atmospheric CO2 and the stomatal index of land plant leaves, we reconstruct Late Cretaceous-Early Tertiary atmospheric CO2 concentration (pCO2) levels with special emphasis on providing a pCO2 estimate directly above the KTB. Our record shows stable Late Cretaceous/Early Tertiary background pCO2 levels of 350–500 ppm by volume, but with a marked increase to at least 2,300 ppm by volume within 10,000 years of the KTB. Numerical simulations with a global biogeochemical carbon cycle model indicate that CO2 outgassing during the eruption of the Deccan Trap basalts fails to fully account for the inferred pCO2 increase. Instead, we calculate that the postboundary pCO2 rise is most consistent with the instantaneous transfer of ≈4,600 Gt C from the lithic to the atmospheric reservoir by a large extraterrestrial bolide impact. A resultant climatic forcing of +12 W⋅m−2 would have been sufficient to warm the Earth's surface by ≈7.5°C, in the absence of counter forcing by sulfate aerosols. This finding reinforces previous evidence for major climatic warming after the KTB impact and implies that severe and abrupt global warming during the earliest Paleocene was an important factor in biotic extinction at the KTB. PMID:12060729

  5. Characteristics of NaNO3-Promoted CdO as a Midtemperature CO2 Absorbent.

    PubMed

    Kim, Kang-Yeong; Kwak, Jin-Su; An, Young-In; Oh, Kyung-Ryul; Kwon, Young-Uk

    2017-06-28

    In this study, we explored the reaction system CdO(s) + CO 2 (g) ⇄ CdCO 3 (s) as a model system for CO 2 capture agent in the intermediate temperature range of 300-400 °C. While pure CdO does not react with CO 2 at all up to 500 °C, CdO mixed with an appropriate amount of NaNO 3 (optimal molar ratio NaNO 3 /CdO = 0.14) greatly enhances the conversion of CdO into CdCO 3 up to ∼80% (5.68 mmol/g). These NaNO 3 -promoted CdO absorbents can undergo many cycles of absorption and desorption by temperature swing between 300 and 370 °C under a 100% CO 2 condition. Details of how NaNO 3 promotes the CO 2 absorption of CdO have been delineated through various techniques using thermogravimetry, coupled with X-ray diffraction and electron microscopy. On the basis of the observed data, we propose a mechanism of CO 2 absorption and desorption of NaNO 3 -promoted CdO. The absorption proceeds through a sequence of events of CO 2 adsorption on the CdO surface covered by NaNO 3 , dissolution of so-formed CdCO 3 , and precipitation of CdCO 3 particles in the NaNO 3 medium. The desorption occurs through the decomposition of CdCO 3 in the dissolved state in the NaNO 3 medium where CdO nanoparticles are formed dispersed in the NaNO 3 medium. The CdO nanoparticles are aggregated into micrometer-large particles with smooth surfaces and regular shapes.

  6. Where does CO2 in Antarctica cool the atmosphere ?

    NASA Astrophysics Data System (ADS)

    Schmithüsen, Holger; Notholt, Justus; König-Langlo, Gert; Lemke, Peter; Jung, Thomas

    2016-04-01

    In a recent study we have shown that for the high altitude plateau in Antarctica CO2 causes a surplus in infrared emission to space compared to what is emitted from the surface. This corresponds to a negative greenhouse effect, and is due to the fact that for this region the surface is typically colder than the atmosphere above, opposite to the rest of the world. As a consequence, for this region an increase in CO2 leads to an increase in the energy loss to space, leading to an increase in the negative greenhouse effect. We now studied in more detail the radiative effect of CO2 and compared the results with available measurements from Antarctica. H. Schmithüsen, J. Notholt, G. Köngig-Langlo, T, Jung. How increasing CO2 leads to an increased negative greenhouse effect in Antarctica. Geophysical Research Letters, in press, 2015. doi: 10.1002/2015GL066749.

  7. Separation of biospheric and fossil fuel fluxes of CO2 by atmospheric inversion of CO2 and 14CO2 measurements: Observation System Simulations

    NASA Astrophysics Data System (ADS)

    Basu, Sourish; Bharat Miller, John; Lehman, Scott

    2016-05-01

    National annual total CO2 emissions from combustion of fossil fuels are likely known to within 5-10 % for most developed countries. However, uncertainties are inevitably larger (by unknown amounts) for emission estimates at regional and monthly scales, or for developing countries. Given recent international efforts to establish emission reduction targets, independent determination and verification of regional and national scale fossil fuel CO2 emissions are likely to become increasingly important. Here, we take advantage of the fact that precise measurements of 14C in CO2 provide a largely unbiased tracer for recently added fossil-fuel-derived CO2 in the atmosphere and present an atmospheric inversion technique to jointly assimilate observations of CO2 and 14CO2 in order to simultaneously estimate fossil fuel emissions and biospheric exchange fluxes of CO2. Using this method in a set of Observation System Simulation Experiments (OSSEs), we show that given the coverage of 14CO2 measurements available in 2010 (969 over North America, 1063 globally), we can recover the US national total fossil fuel emission to better than 1 % for the year and to within 5 % for most months. Increasing the number of 14CO2 observations to ˜ 5000 per year over North America, as recently recommended by the National Academy of Science (NAS) (Pacala et al., 2010), we recover monthly emissions to within 5 % for all months for the US as a whole and also for smaller, highly emissive regions over which the specified data coverage is relatively dense, such as for the New England states or the NY-NJ-PA tri-state area. This result suggests that, given continued improvement in state-of-the art transport models, a measurement program similar in scale to that recommended by the NAS can provide for independent verification of bottom-up inventories of fossil fuel CO2 at the regional and national scale. In addition, we show that the dual tracer inversion framework can detect and minimize biases in

  8. Interaction Between CO2-Rich Sulfate Solutions and Carbonate Reservoir Rocks from Atmospheric to Supercritical CO2 Conditions: Experiments and Modeling

    NASA Astrophysics Data System (ADS)

    Cama, J.; Garcia-Rios, M.; Luquot, L.; Soler Matamala, J. M.

    2014-12-01

    A test site for CO2 geological storage is situated in Hontomín (Spain) with a reservoir rock that is mainly composed of limestone. During and after CO2 injection, the resulting CO2-rich acid brine gives rise to the dissolution of carbonate minerals (calcite and dolomite) and gypsum (or anhydrite at depth) may precipitate since the reservoir brine contains sulfate. Experiments using columns filled with crushed limestone or dolostone were conducted under different P-pCO2 conditions (atmospheric: 1-10-3.5 bar; subcritical: 10-10 bar; and supercritical: 150-34 bar), T (25, 40 and 60 ºC) and input solution compositions (gypsum-undersaturated and gypsum-equilibrated solutions). We evaluated the effect of these parameters on the coupled reactions of calcite/dolomite dissolution and gypsum/anhydrite precipitation. The CrunchFlow and PhreeqC (v.3) numerical codes were used to perform reactive transport simulations of the experiments. Under the P-pCO2-T conditions, the volume of precipitated gypsum was smaller than the volume of dissolved carbonate minerals, yielding an increase in porosity (Δporosity up to ≈ 4%). A decrease in T favored limestone dissolution regardless of pCO2 owing to increasing undersaturation with decreasing temperature. However, gypsum precipitation was favored at high T and under atmospheric pCO2 conditions but not at high T and under 10 bar of pCO2 conditions. The increase in limestone dissolution with pCO2 was directly attributed to pH, which was more acidic at higher pCO2. Increasing pCO2, carbonate dissolution occurred along the column whereas it was localized in the very inlet under atmospheric conditions. This was due to the buffer capacity of the carbonic acid, which maintains pH at around 5 and keeps the solution undersaturated with respect to calcite and dolomite along the column. 1D reactive transport simulations reproduced the experimental data (carbonate dissolution and gypsum precipitation for different P-pCO2-T conditions). Drawing

  9. Control of Atmospheric CO2 by the Ocean's Biological Pump and Shelf-Basin Fractionation

    NASA Astrophysics Data System (ADS)

    Anderson, R. F.; Fleisher, M. Q.; Mix, A. C.

    2006-12-01

    Identifying the cause of the dramatic correlation between atmospheric CO2 concentrations and past climate variability has been one of the principal goals of paleoclimate research over the past quarter century. Several plausible mechanisms have been proposed, and each has been rejected as being incapable by itself of accounting for the full range (80 to 100 ppm) of glacial to interglacial variability of atmospheric CO2 concentration. Consequently, recent studies have focused on scenarios by which a combination of mechanisms work synergistically to account for the full range of CO2 variability. We will present evidence from equatorial Pacific sediment cores that increased strength of the ocean's biological pump was primarily responsible for drawdown of atmospheric CO2 during the early stages of glaciation, and that increased ocean alkalinity (or, more specifically, an increase in the ocean carbonate ion concentration) led to a further reduction of atmospheric CO2 during maximum glaciation. Increased strength of the biological pump is manifest as increasing differences between the carbon isotope composition of planktonic and benthic foraminifera during early stages of glaciation, as predicted a quarter century ago in classic works by Broecker and by Shackleton. Increased carbonate ion concentration is manifest by increased preservation and burial of calcium carbonate in deep equatorial Pacific sediments. The carbon isotope record is noisy, but the pattern is repeated over each of the past three glacial cycles, lending confidence to its reliability. Increased preservation and burial of CaCO3 occurred each time the oxygen isotope composition of benthic foraminifera rose above a threshold value corresponding to a sea level lowering of roughly 70 m below present. This relationship is reproduced systematically throughout the past 450 kyr, again lending confidence to the finding and supporting the view that shelf-basin fractionation, or the shift in CaCO3 deposition from

  10. Sea level fall during glaciation stabilized atmospheric CO2 by enhanced volcanic degassing

    PubMed Central

    Hasenclever, Jörg; Knorr, Gregor; Rüpke, Lars H.; Köhler, Peter; Morgan, Jason; Garofalo, Kristin; Barker, Stephen; Lohmann, Gerrit; Hall, Ian R.

    2017-01-01

    Paleo-climate records and geodynamic modelling indicate the existence of complex interactions between glacial sea level changes, volcanic degassing and atmospheric CO2, which may have modulated the climate system’s descent into the last ice age. Between ∼85 and 70 kyr ago, during an interval of decreasing axial tilt, the orbital component in global temperature records gradually declined, while atmospheric CO2, instead of continuing its long-term correlation with Antarctic temperature, remained relatively stable. Here, based on novel global geodynamic models and the joint interpretation of paleo-proxy data as well as biogeochemical simulations, we show that a sea level fall in this interval caused enhanced pressure-release melting in the uppermost mantle, which may have induced a surge in magma and CO2 fluxes from mid-ocean ridges and oceanic hotspot volcanoes. Our results reveal a hitherto unrecognized negative feedback between glaciation and atmospheric CO2 predominantly controlled by marine volcanism on multi-millennial timescales of ∼5,000–15,000 years. PMID:28681844

  11. Covariation of deep Southern Ocean oxygenation and atmospheric CO2 through the last ice age.

    PubMed

    Jaccard, Samuel L; Galbraith, Eric D; Martínez-García, Alfredo; Anderson, Robert F

    2016-02-11

    No single mechanism can account for the full amplitude of past atmospheric carbon dioxide (CO2) concentration variability over glacial-interglacial cycles. A build-up of carbon in the deep ocean has been shown to have occurred during the Last Glacial Maximum. However, the mechanisms responsible for the release of the deeply sequestered carbon to the atmosphere at deglaciation, and the relative importance of deep ocean sequestration in regulating millennial-timescale variations in atmospheric CO2 concentration before the Last Glacial Maximum, have remained unclear. Here we present sedimentary redox-sensitive trace-metal records from the Antarctic Zone of the Southern Ocean that provide a reconstruction of transient changes in deep ocean oxygenation and, by inference, respired carbon storage throughout the last glacial cycle. Our data suggest that respired carbon was removed from the abyssal Southern Ocean during the Northern Hemisphere cold phases of the deglaciation, when atmospheric CO2 concentration increased rapidly, reflecting--at least in part--a combination of dwindling iron fertilization by dust and enhanced deep ocean ventilation. Furthermore, our records show that the observed covariation between atmospheric CO2 concentration and abyssal Southern Ocean oxygenation was maintained throughout most of the past 80,000 years. This suggests that on millennial timescales deep ocean circulation and iron fertilization in the Southern Ocean played a consistent role in modifying atmospheric CO2 concentration.

  12. How increasing CO2 leads to an increased negative greenhouse effect in Antarctica

    NASA Astrophysics Data System (ADS)

    Schmithüsen, Holger; Notholt, Justus; König-Langlo, Gert; Lemke, Peter; Jung, Thomas

    2015-12-01

    CO2 is the strongest anthropogenic forcing agent for climate change since preindustrial times. Like other greenhouse gases, CO2 absorbs terrestrial surface radiation and causes emission from the atmosphere to space. As the surface is generally warmer than the atmosphere, the total long-wave emission to space is commonly less than the surface emission. However, this does not hold true for the high elevated areas of central Antarctica. For this region, the emission to space is higher than the surface emission; and the greenhouse effect of CO2 is around zero or even negative, which has not been discussed so far. We investigated this in detail and show that for central Antarctica an increase in CO2 concentration leads to an increased long-wave energy loss to space, which cools the Earth-atmosphere system. These findings for central Antarctica are in contrast to the general warming effect of increasing CO2.

  13. Distribution of CO2 in Saturn's Atmosphere from Cassini/cirs Infrared Observations

    NASA Astrophysics Data System (ADS)

    Abbas, M. M.; LeClair, A.; Woodard, E.; Young, M.; Stanbro, M.; Flasar, F. M.; Kunde, V. G.; Achterberg, R. K.; Bjoraker, G.; Brasunas, J.; Jennings, D. E.; the Cassini/CIRS Team

    2013-10-01

    This paper focuses on the CO2 distribution in Saturn's atmosphere based on analysis of infrared spectral observations of Saturn made by the Composite Infrared Spectrometer aboard the Cassini spacecraft. The Cassini spacecraft was launched in 1997 October, inserted in Saturn's orbit in 2004 July, and has been successfully making infrared observations of Saturn, its rings, Titan, and other icy satellites during well-planned orbital tours. The infrared observations, made with a dual Fourier transform spectrometer in both nadir- and limb-viewing modes, cover spectral regions of 10-1400 cm-1, with the option of variable apodized spectral resolutions from 0.53 to 15 cm-1. An analysis of the observed spectra with well-developed radiative transfer models and spectral inversion techniques has the potential to provide knowledge of Saturn's thermal structure and composition with global distributions of a series of gases. In this paper, we present an analysis of a large observational data set for retrieval of Saturn's CO2 distribution utilizing spectral features of CO2 in the Q-branch of the ν2 band, and discuss its possible relationship to the influx of interstellar dust grains. With limited spectral regions available for analysis, due to low densities of CO2 and interference from other gases, the retrieved CO2 profile is obtained as a function of a model photochemical profile, with the retrieved values at atmospheric pressures in the region of ~1-10 mbar levels. The retrieved CO2 profile is found to be in good agreement with the model profile based on Infrared Space Observatory measurements with mixing ratios of ~4.9 × 10-10 at atmospheric pressures of ~1 mbar.

  14. Model Atmospheres of Irradiated Exoplanets: The Influence of Stellar Parameters, Metallicity, and the C/O Ratio

    NASA Astrophysics Data System (ADS)

    Mollière, P.; van Boekel, R.; Dullemond, C.; Henning, Th.; Mordasini, C.

    2015-11-01

    Many parameters constraining the spectral appearance of exoplanets are still poorly understood. We therefore study the properties of irradiated exoplanet atmospheres over a wide parameter range including metallicity, C/O ratio, and host spectral type. We calculate a grid of 1D radiative-convective atmospheres and emission spectra. We perform the calculations with our new Pressure-Temperature Iterator and Spectral Emission Calculator for Planetary Atmospheres (PETIT) code, assuming chemical equilibrium. The atmospheric structures and spectra are made available online. We find that atmospheres of planets with C/O ratios ˜1 and {T}{{eff}} ≳ 1500 K can exhibit inversions due to heating by the alkalis because the main coolants CH4, H2O, and HCN are depleted. Therefore, temperature inversions possibly occur without the presence of additional absorbers like TiO and VO. At low temperatures we find that the pressure level of the photosphere strongly influences whether the atmospheric opacity is dominated by either water (for low C/O) or methane (for high C/O), or both (regardless of the C/O). For hot, carbon-rich objects this pressure level governs whether the atmosphere is dominated by methane or HCN. Further we find that host stars of late spectral type lead to planetary atmospheres which have shallower, more isothermal temperature profiles. In agreement with prior work we find that for planets with {T}{{eff}}\\lt 1750 K the transition between water or methane dominated spectra occurs at C/O ˜ 0.7, instead of ˜1, because condensation preferentially removes oxygen.

  15. An attempt at estimating Paris area CO2 emissions from atmospheric concentration measurements

    NASA Astrophysics Data System (ADS)

    Bréon, F. M.; Broquet, G.; Puygrenier, V.; Chevallier, F.; Xueref-Remy, I.; Ramonet, M.; Dieudonné, E.; Lopez, M.; Schmidt, M.; Perrussel, O.; Ciais, P.

    2015-02-01

    Atmospheric concentration measurements are used to adjust the daily to monthly budget of fossil fuel CO2 emissions of the Paris urban area from the prior estimates established by the Airparif local air quality agency. Five atmospheric monitoring sites are available, including one at the top of the Eiffel Tower. The atmospheric inversion is based on a Bayesian approach, and relies on an atmospheric transport model with a spatial resolution of 2 km with boundary conditions from a global coarse grid transport model. The inversion adjusts prior knowledge about the anthropogenic and biogenic CO2 fluxes from the Airparif inventory and an ecosystem model, respectively, with corrections at a temporal resolution of 6 h, while keeping the spatial distribution from the emission inventory. These corrections are based on assumptions regarding the temporal autocorrelation of prior emissions uncertainties within the daily cycle, and from day to day. The comparison of the measurements against the atmospheric transport simulation driven by the a priori CO2 surface fluxes shows significant differences upwind of the Paris urban area, which suggests a large and uncertain contribution from distant sources and sinks to the CO2 concentration variability. This contribution advocates that the inversion should aim at minimising model-data misfits in upwind-downwind gradients rather than misfits in mole fractions at individual sites. Another conclusion of the direct model-measurement comparison is that the CO2 variability at the top of the Eiffel Tower is large and poorly represented by the model for most wind speeds and directions. The model's inability to reproduce the CO2 variability at the heart of the city makes such measurements ill-suited for the inversion. This and the need to constrain the budgets for the whole city suggests the assimilation of upwind-downwind mole fraction gradients between sites at the edge of the urban area only. The inversion significantly improves the agreement

  16. The High Accuracy Measurement of CO2 Mixing Ratio Profiles Using Ground Based 1.6 μm CO2-DIAL with Temperature Measurement Techniques in the Lower-Atmosphere

    NASA Astrophysics Data System (ADS)

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

    2017-12-01

    We have developed a ground based direct detection three-wavelength 1.6 μm differential absorption lidar (DIAL) to achieve measurements of vertical CO2 concentration and temperature profiles in the atmosphere. As the spectra of absorption lines of any molecules are influenced basically by the temperature and pressure in the atmosphere, it is important to measure them simultaneously so that the better accuracy of the DIAL measurement is realized. Conventionally, we have obtained the vertical profile of absorption cross sections using the atmospheric temperature profile by the objective analysis and the atmospheric pressure profile calculated by the pressure height equation. Comparison of atmospheric pressure profiles calculated from this equation and those obtained from radiosonde observations at Tateno, Japan is consistent within 0.2 % below 3 km altitude. But the temperature dependency of the CO2 density is 0.25 %/°C near the surface. Moreover, the CO2 concentration is often evaluated by the mixing ratio. Because the air density is related by the ideal gas law, the mixing ratio is also related by the atmospheric temperature. Therefore, the temperature affects not only accuracy of CO2 concentration but the CO2 mixing ratio. In this paper, some experimental results of the simultaneous measurement of atmospheric temperature profiles and CO2 mixing ratio profiles are reported from 0.4 to 2.5 km altitude using the three-wavelength 1.6 μm DIAL system. Temperature profiles of CO2 DIAL measurement were sometimes different from those of objective analysis below 1.5 km altitude. These differences are considered to be due to regionality at the lidar site. The temperature difference of 5.0 °C corresponds to a CO2 mixing ratio difference of 8.0 ppm at 500 m altitude. This cannot be ignored in estimates of regional sources and sinks of CO2. This three-wavelength CO2 DIAL technique can estimate accurately temporal behavior of CO2 mixing ratio profiles in the lower atmosphere

  17. Regional US carbon sinks from three-dimensional atmospheric CO2 sampling

    PubMed Central

    Crevoisier, Cyril; Sweeney, Colm; Gloor, Manuel; Sarmiento, Jorge L.; Tans, Pieter P.

    2010-01-01

    Studies diverge substantially on the actual magnitude of the North American carbon budget. This is due to the lack of appropriate data and also stems from the difficulty to properly model all the details of the flux distribution and transport inside the region of interest. To sidestep these difficulties, we use here a simple budgeting approach to estimate land-atmosphere fluxes across North America by balancing the inflow and outflow of CO2 from the troposphere. We base our study on the unique sampling strategy of atmospheric CO2 vertical profiles over North America from the National Oceanic and Atmospheric Administration/Earth System Research Laboratory aircraft network, from which we infer the three-dimensional CO2 distribution over the continent. We find a moderate sink of 0.5 ± 0.4 PgC y-1 for the period 2004–2006 for the coterminous United States, in good agreement with the forest-inventory-based estimate of the first North American State of the Carbon Cycle Report, and averaged climate conditions. We find that the highest uptake occurs in the Midwest and in the Southeast. This partitioning agrees with independent estimates of crop uptake in the Midwest, which proves to be a significant part of the US atmospheric sink, and of secondary forest regrowth in the Southeast. Provided that vertical profile measurements are continued, our study offers an independent means to link regional carbon uptake to climate drivers. PMID:20937899

  18. Laser Sounder Approach for Measuring Atmospheric CO2 from Orbit

    NASA Technical Reports Server (NTRS)

    Krainak, Michael A.; Andrews, Arlyn E.; Allan, Graham R.; Burris, John F.; Collatz, G. James; Riris, Harris; Stephen, Mark A.; Sun, Xiao-Li; Abshire, James B.

    2004-01-01

    We report on an active remote sensing approach using an erbium fiber amplifier based transmitter for atmospheric CO2 measurements in an overtone band near 1.57 microns and initial horizontal path measurements to less than 1% precision.

  19. An attempt at estimating Paris area CO2 emissions from atmospheric concentration measurements

    NASA Astrophysics Data System (ADS)

    Bréon, F. M.; Broquet, G.; Puygrenier, V.; Chevallier, F.; Xueref-Rémy, I.; Ramonet, M.; Dieudonné, E.; Lopez, M.; Schmidt, M.; Perrussel, O.; Ciais, P.

    2014-04-01

    Atmospheric concentration measurements are used to adjust the daily to monthly budget of CO2 emissions from the AirParif inventory of the Paris agglomeration. We use 5 atmospheric monitoring sites including one at the top of the Eiffel tower. The atmospheric inversion is based on a Bayesian approach, and relies on an atmospheric transport model with a spatial resolution of 2 km with boundary conditions from a global coarse grid transport model. The inversion tool adjusts the CO2 fluxes (anthropogenic and biogenic) with a temporal resolution of 6 h, assuming temporal correlation of emissions uncertainties within the daily cycle and from day to day, while keeping the a priori spatial distribution from the emission inventory. The inversion significantly improves the agreement between measured and modelled concentrations. However, the amplitude of the atmospheric transport errors is often large compared to the CO2 gradients between the sites that are used to estimate the fluxes, in particular for the Eiffel tower station. In addition, we sometime observe large model-measurement differences upwind from the Paris agglomeration, which confirms the large and poorly constrained contribution from distant sources and sinks included in the prescribed CO2 boundary conditions These results suggest that (i) the Eiffel measurements at 300 m above ground cannot be used with the current system and (ii) the inversion shall rely on the measured upwind-downwind gradients rather than the raw mole fraction measurements. With such setup, realistic emissions are retrieved for two 30 day periods. Similar inversions over longer periods are necessary for a proper evaluation of the results.

  20. A 490 W transversely excited atmospheric CO2 spark gap laser with added H2

    NASA Astrophysics Data System (ADS)

    Zand, M.; Koushki, A. M.; Neshati, R.; Kia, B.; Khorasani, K.

    2018-02-01

    In this paper we present a new design for a high pulse repetition rate transversely excited atmospheric CO2 laser with ultraviolet pre-ionization. A new method of fast thyristor capacitor charging and discharging by a spark gap is used. The effect of H2 gas addition on the output and stability of a transversely excited atmospheric laser operating with a basic mixture of CO2, N2 and He is investigated. The output power was increased by adding H2 to the gas mixture ratio of CO2:N2:He:H2  =  1:1:8:0.5 at total pressure of 850 mbar. An average power of 490 W at 110 Hz with 4.5 J per pulse was obtained. The laser efficiency was 11.2% and oxygen gas was used in the spark gap for electron capture to reduce the recovery time and increase the repetition rate.

  1. Atmospheric CO2 effect on stable carbon isotope composition of terrestrial fossil archives.

    PubMed

    Hare, Vincent J; Loftus, Emma; Jeffrey, Amy; Ramsey, Christopher Bronk

    2018-01-17

    The 13 C/ 12 C ratio of C 3 plant matter is thought to be controlled by the isotopic composition of atmospheric CO 2 and stomatal response to environmental conditions, particularly mean annual precipitation (MAP). The effect of CO 2 concentration on 13 C/ 12 C ratios is currently debated, yet crucial to reconstructing ancient environments and quantifying the carbon cycle. Here we compare high-resolution ice core measurements of atmospheric CO 2 with fossil plant and faunal isotope records. We show the effect of pCO 2 during the last deglaciation is stronger for gymnosperms (-1.4 ± 1.2‰) than angiosperms/fauna (-0.5 ± 1.5‰), while the contributions from changing MAP are -0.3 ± 0.6‰ and -0.4 ± 0.4‰, respectively. Previous studies have assumed that plant 13 C/ 12 C ratios are mostly determined by MAP, an assumption which is sometimes incorrect in geological time. Atmospheric effects must be taken into account when interpreting terrestrial stable carbon isotopes, with important implications for past environments and climates, and understanding plant responses to climate change.

  2. Implications of 'Peak Oil' for Atmospheric CO2 and Climate

    NASA Astrophysics Data System (ADS)

    Kharecha, P. A.; Hansen, J. E.

    2008-12-01

    Unconstrained CO2 emission from fossil fuel burning has been the dominant cause of observed anthropogenic global warming. The amounts of "proven" and potential fossil fuel reserves are uncertain and debated. Regardless of the true values, society has flexibility in the degree to which it chooses to exploit these reserves, especially unconventional fossil fuels and those located in extreme or pristine environments. If conventional oil production peaks within the next few decades, it may have a large effect on future atmospheric CO2 and climate change, depending upon subsequent energy choices. Assuming that proven oil and gas reserves do not greatly exceed estimates of the Energy Information Administration -- and recent trends are toward lower estimates -- we show that it is feasible to keep atmospheric CO2 from exceeding about 450 ppm by 2100, provided that emissions from coal, unconventional fossil fuels, and land use are constrained. Coal-fired facilities without sequestration must be phased out before midcentury to achieve this CO2 limit. It is also important to "stretch" conventional oil reserves via energy conservation and efficiency, thus averting strong pressures to extract liquid fuels from coal or unconventional fossil fuels while clean technologies are being developed for the era "beyond fossil fuels". We argue that a rising price on carbon emissions is needed to discourage conversion of the vast fossil resources into usable reserves, and to keep CO2 below 450 ppm. It is also plausible that CO2 can be returned below 350 ppm by 2100 or sooner, if more aggressive mitigation measures are enacted, most notably a phase-out of global coal emissions by circa 2030 and large- scale reforestation, primarily in the tropics but also in temperate regions.

  3. Delta14 CO2 Atmospheric Record from Schauinsland, Germany

    DOE Data Explorer

    Levin, Ingeborg [Institut fur Umweltphysik, University of Heidelberg, Heidelberg, Germany; Kromer, Bernd [Institut fur Umweltphysik, University of Heidelberg, Heidelberg, Germany

    1997-01-01

    All air samples at Schauinsland have been collected from a ventilated intake stack approximately 7m above the ground. Bi-weekly integrated CO2 samples from about 15-20 m3 of air have been continuously collected by dynamic quantitative absorption in carbonate-free sodium hydroxide (NaOH) solution. Air has been pumped through a rotating glass tube filled with a packed bed of Raschig rings (hard glass) to enlarge the surface of the absorbing NaOH solution (200 ml of 4 normal NaOH). The CO2 absorption is quantitative and samples represent mean values of 10 days to 2 weeks. In the laboratory, the samples are extracted from the NaOH solution in a vacuum system by adding hydrochloric or sulfuric acid. 13C analyses of the CO2 are by mass spectrometry and 14C analyses are by high precision proportional counting, after purification of the CO2 sample over charcoal (Schoch et al. 1980, Kromer and Münnich 1992). δ13C values are given relative to the V-PDB standard (Hut 1987) with the overall precision of a single analysis reported to be +/- 0.15 per mil (Levin and Kromer 1997). δ14C data are given relative to the NIST oxalic acid activity corrected for decay (Stuiver and Polach 1977) with the precision of a single δ14C measurement reported to be +/- 3-5 per mil (Levin and Kromer 1997).

  4. [Diurnal and seasonal variations of surface atmospheric CO2 concentration in the river estuarine marsh].

    PubMed

    Zhang, Lin-Hai; Tong, Chuan; Zeng, Cong-Sheng

    2014-03-01

    Characteristics of diurnal and seasonal variations of surface atmospheric CO2 concentration were analyzed in the Minjiang River estuarine marsh from December 2011 to November 2012. The results revealed that both the diurnal and seasonal variation of surface atmospheric CO2 concentration showed single-peak patterns, with the valley in the daytime and the peak value at night for the diurnal variations, and the maxima in winter and minima in summer for the seasonal variation. Diurnal amplitude of CO2 concentration varied from 16.96 micromol x mol(-1) to 38.30 micromol x mol(-1). The seasonal averages of CO2 concentration in spring, summer, autumn and winter were (353.74 +/- 18.35), (327.28 +/- 8.58), (354.78 +/- 14.76) and (392.82 +/- 9.71) micromol x mol(-1), respectively, and the annual mean CO2 concentration was (357.16 +/- 26.89) micromol x mol(-1). The diurnal CO2 concentration of surface atmospheric was strongly negatively correlated with temperature, wind speed, photosynthetically active radiation and total solar radiation (P < 0.05). The diurnal concentration of CO2 was negatively related with tidal level in January, but significantly positively related in July.

  5. C/O Ratios in Exoplanetary Atmospheres

    NASA Astrophysics Data System (ADS)

    Madhusudhan, N.

    2012-04-01

    Recent observations are allowing unprecedented constraints on the carbon-to-oxygen (C/O) ratios of giant exoplanetary atmospheres. Elemental abundance ratios, such as the C/O ratio, of planetary atmospheres provide important constraints on planetary interior compositions and formation conditions, and on the chemical and dynamical processes in the atmospheres. In addition, for super-Earths, the potential availability of water and oxygen, and hence the notion of `habitability', is contingent on the C/O ratio. Typically, an oxygen-rich composition, motivated by the solar nebula C/O of 0.5, is assumed in models of exoplanetary formation, interiors, and atmospheres. However, recent observations of exoplanetary atmospheres are suggesting the possibility of C/O ratios of 1.0 or higher, motivating the new class of Carbon-rich Planets (CRPs). In this talk, we will present observational constraints on atmospheric C/O ratios for an ensemble of transiting exoplanets and discuss their implications on the various aspects of exoplanetary characterization described above. Motivated by these results, we propose a two-dimensional classification scheme for irradiated giant exoplanets in which the incident irradiation and the atmospheric C/O ratio are the two dimensions. We demonstrate that some of the extreme anomalies reported in the literature for hot Jupiter atmospheres can be explained based on this 2-D scheme. An overview of new theoretical avenues and observational efforts underway for chemical characterization of extrasolar planets, from hot Jupiters to super-Earths, will be presented.

  6. Infrared atmospheric sounding interferometer correlation interferometry for the retrieval of atmospheric gases: the case of H2O and CO2.

    PubMed

    Grieco, Giuseppe; Masiello, Guido; Serio, Carmine; Jones, Roderic L; Mead, Mohammed I

    2011-08-01

    Correlation interferometry is a particular application of Fourier transform spectroscopy with partially scanned interferograms. Basically, it is a technique to obtain the difference between the spectra of atmospheric radiance at two diverse spectral resolutions. Although the technique could be exploited to design an appropriate correlation interferometer, in this paper we are concerned with the analytical aspects of the method and its application to high-spectral-resolution infrared observations in order to separate the emission of a given atmospheric gas from a spectral signal dominated by surface emission, such as in the case of satellite spectrometers operated in the nadir looking mode. The tool will be used to address some basic questions concerning the vertical spatial resolution of H2O and to develop an algorithm to retrieve the columnar amount of CO2. An application to complete interferograms from the Infrared Atmospheric Sounding Interferometer will be presented and discussed. For H2O, we have concluded that the vertical spatial resolution in the lower troposphere mostly depends on broad features associated with the spectrum, whereas for CO2, we have derived a technique capable of retrieving a CO2 columnar amount with accuracy of ≈±7 parts per million by volume at the level of each single field of view.

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

    NASA Astrophysics Data System (ADS)

    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.

  8. Characterizing Uncertainties in Atmospheric Inversions of Fossil Fuel CO2 Emissions in California

    NASA Astrophysics Data System (ADS)

    Brophy, K. J.; Graven, H. D.; Manning, A.; Arnold, T.; Fischer, M. L.; Jeong, S.; Cui, X.; Parazoo, N.

    2016-12-01

    In 2006 California passed a law requiring greenhouse gas emissions be reduced to 1990 levels by 2020, equivalent to a 20% reduction over 2006-2020. Assessing compliance with greenhouse gas mitigation policies requires accurate determination of emissions, particularly for CO2 emitted by fossil fuel combustion (ffCO2). We found differences in inventory-based ffCO2 flux estimates for California total emissions of 11% (standard deviation relative to the mean), and even larger differences on some smaller sub-state levels. Top-down studies may be useful for validating ffCO2 flux estimates, but top-down studies of CO2 typically focus on biospheric CO2 fluxes and they are not yet well-developed for ffCO2. Implementing top-down studies of ffCO2 requires observations of a fossil fuel combustion tracer such as 14C to distinguish ffCO2 from biospheric CO2. However, even if a large number of 14C observations are available, multiple other sources of uncertainty will contribute to the uncertainty in posterior ffCO2 flux estimates. With a Bayesian inverse modelling approach, we use simulated atmospheric observations of ffCO2 at a network of 11 tower sites across California in an observing system simulation experiment to investigate uncertainties. We use four different prior ffCO2 flux estimates, two different atmospheric transport models, different types of spatial aggregation, and different assumptions for observational and model transport uncertainties to investigate contributions to posterior ffCO2 emission uncertainties. We show how various sources of uncertainty compare and which uncertainties are likely to limit top-down estimation of ffCO2 fluxes in California.

  9. The stomatal CO2 proxy does not saturate at high atmospheric CO2 concentrations: evidence from stomatal index responses of Araucariaceae conifers.

    PubMed

    Haworth, Matthew; Elliott-Kingston, Caroline; McElwain, Jennifer C

    2011-09-01

    The inverse relationship between the number of stomata on a leaf surface and the atmospheric carbon dioxide concentration ([CO(2)]) in which the leaf developed allows plants to optimise water-use efficiency (WUE), but it also permits the use of fossil plants as proxies of palaeoatmospheric [CO(2)]. The ancient conifer family Araucariaceae is often represented in fossil floras and may act as a suitable proxy of palaeo-[CO(2)], yet little is known regarding the stomatal index (SI) responses of extant Araucariaceae to [CO(2)]. Four Araucaria species (Araucaria columnaris, A. heterophylla, A. angustifolia and A. bidwillii) and Agathis australis displayed no significant relationship in SI to [CO(2)] below current ambient levels (~380 ppm). However, representatives of the three extant genera within the Araucariaceae (A. bidwillii, A. australis and Wollemia nobilis) all exhibited significant reductions in SI when grown in atmospheres of elevated [CO(2)] (1,500 ppm). Stomatal conductance was reduced and WUE increased when grown under elevated [CO(2)]. Stomatal pore length did not increase alongside reduced stomatal density (SD) and SI in the three araucariacean conifers when grown at elevated [CO(2)]. These pronounced SD and SI reductions occur at higher [CO(2)] levels than in other species with more recent evolutionary origins, and may reflect an evolutionary legacy of the Araucariaceae in the high [CO(2)] world of the Mesozoic Era. Araucariacean conifers may therefore be suitable stomatal proxies of palaeo-[CO(2)] during periods of "greenhouse" climates and high [CO(2)] in the Earth's history.

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

    NASA Astrophysics Data System (ADS)

    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 aestivumCO2 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

  11. Development and Evaluation of a High Sensitivity DIAL System for Profiling Atmospheric CO2

    NASA Technical Reports Server (NTRS)

    Ismail, Syed; Koch, Grady J.; Refaat, Tamer F.; Abedin, M. N.; Yu, Jirong; Singh, Upendra N.

    2008-01-01

    A ground-based 2-micron Differential Absorption Lidar (DIAL) CO2 profiling system for atmospheric boundary layer studies and validation of space-based CO2 sensors is being developed and tested at NASA Langley Research Center as part of the NASA Instrument Incubator Program. To capture the variability of CO2 in the lower troposphere a precision of 1-2 ppm of CO2 (less than 0.5%) with 0.5 to 1 km vertical resolution from near surface to free troposphere (4-5 km) is one of the goals of this program. In addition, a 1% (3 ppm) absolute accuracy with a 1 km resolution over 0.5 km to free troposphere (4-5 km) is also a goal of the program. This DIAL system leverages 2-micron laser technology developed under NASA's Laser Risk Reduction Program (LRRP) and other NASA programs to develop new solid-state laser technology that provides high pulse energy, tunable, wavelength-stabilized, and double-pulsed lasers that are operable over pre-selected temperature insensitive strong CO2 absorption lines suitable for profiling of lower tropospheric CO2. It also incorporates new high quantum efficiency, high gain, and relatively low noise phototransistors, and a new receiver/signal processor system to achieve high precision DIAL measurements. This presentation describes the capabilities of this system for atmospheric CO2 and aerosol profiling. Examples of atmospheric measurements in the lidar and DIAL mode will be presented.

  12. Miniaturized Laser Heterodyne Radiometer for Measurements of CO2 in the Atmospheric Column

    NASA Technical Reports Server (NTRS)

    Wilson, E. L.; Mclinden, M. L.; Miller, J. H.; Allan, G. R.; Lott, L. E.; Melroy, H. R.; Clarke, G. B.

    2013-01-01

    We have developed a low-cost, miniaturized laser heterodyne radiometer for highly sensitive measurements of carbon dioxide (CO2) in the atmospheric column. In this passive design, sunlight that has undergone absorption by CO2 in the atmosphere is collected and mixed with continuous wave laser light that is step-scanned across the absorption feature centered at 1,573.6 nm. The resulting radio frequency beat signal is collected as a function of laser wavelength, from which the total column mole fraction can be de-convolved. We are expanding this technique to include methane (CH4) and carbon monoxide (CO), and with minor modifications, this technique can be expanded to include species such as water vapor (H2O) and nitrous oxide (N2O).

  13. Competing Atmospheric and Surface-Driven Impacts of Absorbing Aerosols on the East Asian Summer Monsoon

    NASA Astrophysics Data System (ADS)

    Persad, G.; Paynter, D.; Ming, Y.; Ramaswamy, V.

    2015-12-01

    Absorbing aerosols, by attenuating shortwave radiation within the atmosphere and reemitting it as longwave radiation, redistribute energy both vertically within the surface-atmosphere column and horizontally between polluted and unpolluted regions. East Asia has the largest concentrations of anthropogenic absorbing aerosols globally, and these, along with the region's scattering aerosols, have both reduced the amount of solar radiation reaching the Earth's surface regionally ("solar dimming") and increased shortwave absorption within the atmosphere, particularly during the peak months of the East Asian Summer Monsoon (EASM). We here analyze how atmospheric absorption and surface solar dimming compete in driving the response of EASM circulation to anthropogenic absorbing aerosols, which dominates, and why—issues of particular importance for predicting how the EASM will respond to projected changes in absorbing and scattering aerosol emissions in the future. We probe these questions in a state-of-the-art general circulation model (GCM) using a combination of realistic and idealized aerosol perturbations that allow us to analyze the relative influence of absorbing aerosols' atmospheric and surface-driven impacts on EASM circulation. In combination, our results make clear that, although absorption-driven dimming has a less detrimental effect on EASM circulation than purely scattering-driven dimming, aerosol absorption is still a net impairment to EASM strength when both its atmospheric and surface effects are considered. Because atmospheric heating is not efficiently conveyed to the surface, the surface dimming and associated cooling from even a pure absorber is sufficient to counteract its atmospheric heating, resulting in a net reduction in EASM strength. These findings elevate the current understanding of the impacts of aerosol absorption on the EASM, improving our ability to diagnose EASM responses to current and future regional changes in aerosol emissions.

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

    NASA Astrophysics Data System (ADS)

    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

  15. Reproducibility of Holocene atmospheric CO 2 records based on stomatal frequency

    NASA Astrophysics Data System (ADS)

    Wagner, Friederike; Kouwenberg, Lenny L. R.; van Hoof, Thomas B.; Visscher, Henk

    2004-10-01

    The majority of the stomatal frequency-based estimates of CO2 for the Holocene do not support the widely accepted concept of comparably stable CO2 concentrations throughout the past 11,500 years. To address the critique that these stomatal frequency variations result from local environmental change or methodological insufficiencies, multiple stomatal frequency records were compared for three climatic key periods during the Holocene, namely the Preboreal oscillation, the 8.2 kyr cooling event and the Little Ice Age. The highly comparable fluctuations in the palaeo-atmospheric CO2 records, which were obtained from different continents and plant species (deciduous angiosperms as well as conifers) using varying calibration approaches, provide strong evidence for the integrity of leaf-based CO2 quantification.

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

    PubMed

    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.

  17. Atmospheric CO2 sequestration in iron and steel slag: Consett, Co. Durham, UK.

    PubMed

    Mayes, William Matthew; Riley, Alex L; Gomes, Helena I; Brabham, Peter; Hamlyn, Joanna; Pullin, Huw; Renforth, Phil

    2018-06-12

    Carbonate formation in waste from the steel industry could constitute a non-trivial proportion of global requirements to remove carbon dioxide from the atmosphere at potentially low cost. To constrain this potential, we examined atmospheric carbon dioxide sequestration in a >20 million tonne legacy slag deposit in northern England, UK. Carbonates formed from the drainage water of the heap had stable carbon and oxygen isotopes between -12 and -25 ‰ and -5 and -18 ‰ for δ13C and δ18O respectively, suggesting atmospheric carbon dioxide sequestration in high pH solutions. From analysis of solution saturation state, we estimate that between 280 and 2,900 tCO2 have precipitated from the drainage waters. However, by combining a thirty-seven-year dataset of the drainage water chemistry with geospatial analysis, we estimate that <1 % of the maximum carbon capture potential of the deposit may have been realised. This implies that uncontrolled deposition of slag is insufficient to maximise carbon sequestration, and there may be considerable quantities of unreacted legacy deposits available for atmospheric carbon sequestration.

  18. CO/sub 2/ and Spaceship Earth

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Terra, S.

    1978-01-01

    Atmospheric CO/sub 2/ concentrations have increased so rapidly since the start of the industrial revolution that the threat of climatic and economic disruptions may require limitations on future fossil-energy production. The greenhouse effect by which longwave radiation is absorbed by CO/sub 2/ and reradiated back to earth, will raise the earth's temperature. Other factors can be traced to a warming trend caused by an increase in nitrous oxides from agricultural activity and a cooling tendency as the added warmth increases evaporation and cloud formation. Several national and international studies of CO/sub 2/ effects are underway and legislation for further datamore » and research has been proposed in Congress. While scientists agree that CO/sub 2/ levels are increasing, they disagree on the nature of the long-term effects on climate, crop production, deglaciation, and the impact of forest and other biological matter. Simulation models for projecting future conditions need to include transients to predict the effects of CO/sub 2/ level changes.« less

  19. Scaling laws for perturbations in the ocean-atmosphere system following large CO2 emissions

    NASA Astrophysics Data System (ADS)

    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 peak perturbations in the atmosphere and ocean variables are then fit to power law functions of the form γDαEbeta, where D is the event duration, E is its total carbon emission, and γ is a coefficient. Good power law fits are obtained for most system variables for E up to 50 000 PgC and D up to 100 kyr. However, these power laws deviate substantially from predictions based on simplified equilibrium considerations. For example, although all of the peak perturbations increase with emission rate E/D, we find no evidence of emission rate-only scaling α + β =0, a prediction of the long-term equilibrium between CO2 input by volcanism and CO2 removal by silicate weathering. Instead, our scaling yields α + β ≃ 1 for total ocean and atmosphere carbon and 0< α + β < 1 for most of the other system variables. The deviations in these scaling laws from equilibrium predictions are mainly due to the multitude and diversity of time scales that govern the exchange of carbon between marine sediments, the ocean, and the atmosphere.

  20. Plastic and adaptive responses of plant respiration to changes in atmospheric CO(2) concentration.

    PubMed

    Gonzàlez-Meler, Miquel A; Blanc-Betes, Elena; Flower, Charles E; Ward, Joy K; Gomez-Casanovas, Nuria

    2009-12-01

    The concentration of atmospheric CO2 has increased from below 200 microl l(-1) during last glacial maximum in the late Pleistocene to near 280 microl l(-1) at the beginning of the Holocene and has continuously increased since the onset of the industrial revolution. Most responses of plants to increasing atmospheric CO2 levels result in increases in photosynthesis, water use efficiency and biomass. Less known is the role that respiration may play during adaptive responses of plants to changes in atmospheric CO2. Although plant respiration does not increase proportionally with CO2-enhanced photosynthesis or growth rates, a reduction in respiratory costs in plants grown at subambient CO2 can aid in maintaining a positive plant C-balance (i.e. enhancing the photosynthesis-to-respiration ratio). The understanding of plant respiration is further complicated by the presence of the alternative pathway that consumes photosynthate without producing chemical energy [adenosine triphosphate (ATP)] as effectively as respiration through the normal cytochrome pathway. Here, we present the respiratory responses of Arabidopsis thaliana plants selected at Pleistocene (200 microl l(-1)), current Holocene (370 microl l(-1)), and elevated (700 microl l(-1)) concentrations of CO2 and grown at current CO2 levels. We found that respiration rates were lower in Pleistocene-adapted plants when compared with Holocene ones, and that a substantial reduction in respiration was because of reduced activity of the alternative pathway. In a survey of the literature, we found that changes in respiration across plant growth forms and CO2 levels can be explained in part by differences in the respiratory energy demand for maintenance of biomass. This trend was substantiated in the Arabidopsis experiment in which Pleistocene-adapted plants exhibited decreases in respiration without concurrent reductions in tissue N content. Interestingly, N-based respiration rates of plants adapted to elevated CO2 also

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

    PubMed

    Gottschalk, Julia; Skinner, Luke C; Lippold, Jörg; Vogel, Hendrik; Frank, Norbert; Jaccard, Samuel L; Waelbroeck, Claire

    2016-05-17

    Millennial-scale climate changes during the last glacial period and deglaciation were accompanied by rapid changes in atmospheric CO2 that remain unexplained. While the role of the Southern Ocean as a 'control valve' on ocean-atmosphere CO2 exchange has been emphasized, the exact nature of this role, in particular the relative contributions of physical (for example, ocean dynamics and air-sea gas exchange) versus biological processes (for example, export productivity), remains poorly constrained. Here we combine reconstructions of bottom-water [O2], export production and (14)C ventilation ages in the sub-Antarctic Atlantic, and show that atmospheric CO2 pulses during the last glacial- and deglacial periods were consistently accompanied by decreases in the biological export of carbon and increases in deep-ocean ventilation via southern-sourced water masses. These findings demonstrate how the Southern Ocean's 'organic carbon pump' has exerted a tight control on atmospheric CO2, and thus global climate, specifically via a synergy of both physical and biological processes.

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

    PubMed Central

    Gottschalk, Julia; Skinner, Luke C.; Lippold, Jörg; Vogel, Hendrik; Frank, Norbert; Jaccard, Samuel L.; Waelbroeck, Claire

    2016-01-01

    Millennial-scale climate changes during the last glacial period and deglaciation were accompanied by rapid changes in atmospheric CO2 that remain unexplained. While the role of the Southern Ocean as a 'control valve' on ocean–atmosphere CO2 exchange has been emphasized, the exact nature of this role, in particular the relative contributions of physical (for example, ocean dynamics and air–sea gas exchange) versus biological processes (for example, export productivity), remains poorly constrained. Here we combine reconstructions of bottom-water [O2], export production and 14C ventilation ages in the sub-Antarctic Atlantic, and show that atmospheric CO2 pulses during the last glacial- and deglacial periods were consistently accompanied by decreases in the biological export of carbon and increases in deep-ocean ventilation via southern-sourced water masses. These findings demonstrate how the Southern Ocean's 'organic carbon pump' has exerted a tight control on atmospheric CO2, and thus global climate, specifically via a synergy of both physical and biological processes. PMID:27187527

  3. Recent slowdown of atmospheric CO2 amplification due to vegetation-climate feedback over northern lands

    NASA Astrophysics Data System (ADS)

    Li, Z.; Xia, J.; Ahlström, A.; Rinke, A.; Koven, C.; Hayes, D. J.; Ji, D.; Zhang, G.; Krinner, G.; Chen, G.; Dong, J.; Liang, J.; Moore, J.; Jiang, L.; Yan, L.; Ciais, P.; Peng, S.; Wang, Y.; Xiao, X.; Shi, Z.; McGuire, A. D.; Luo, Y.

    2017-12-01

    The enhanced vegetation growth by climate warming plays a pivotal role in amplifying the seasonal cycle of atmospheric CO2 at northern high latitudes since 1960s1-3. It remains unclear that whether this mechanism is still robust since 1990s, because a paused vegetation growth increase4,5 and weakened temperature control on CO2 uptake6,7 have been detected during this period. Here, based on in-situ atmospheric CO2 concentration records above northern 50o N, we found a slowdown of the atmospheric CO2 amplification from the mid-1990s to mid-2000s. This phenomenon is associated with the pause of vegetation greening trend and slowdown of spring warming. We further showed that both the vegetation greenness and its growing season length are positively correlated to spring but not autumn temperature from 1982 to 2010 over the northern lands. However, the state-of-art terrestrial biosphere models produce positive responses of gross primary productivity to both spring and autumn warming. These findings emphasize the importance of vegetation-climate feedback in shaping the atmospheric CO2 seasonality, and call for an improved carbon-cycle response to non-uniform seasonal warming at high latitudes in current models.

  4. Agricultural green revolution as a driver of increasing atmospheric CO2 seasonal amplitude

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Zeng, Ning; Zhao, Fang; Collatz, George

    The atmospheric carbon dioxide (CO2) record displays a prominent seasonal cycle that arises mainly from changes in vegetation growth and the corresponding CO2 uptake during the boreal spring and summer growing seasons and CO2 release during the autumn and winter seasons. The CO2 seasonal amplitude has increased over the past five decades, suggesting an increase in Northern Hemisphere biospheric activity. It has been proposed that vegetation growth may have been stimulated by higher concentrations of CO2 as well as by warming in recent decades, but such mechanisms have been unable to explain the full range and magnitude of the observedmore » increase in CO2 seasonal amplitude. Here we suggest that the intensification of agriculture (the Green Revolution, in which much greater crop yield per unit area was achieved by hybridization, irrigation and fertilization) during the past five decades is a driver of changes in the seasonal characteristics of the global carbon cycle. Our analysis of CO2 data and atmospheric inversions shows a robust 15 per cent long-term increase in CO2 seasonal amplitude from 1961 to 2010, punctuated by large decadal and interannual variations. Using a terrestrial carbon cycle model that takes into account high-yield cultivars, fertilizer use and irrigation, we find that the long-term increase in CO2 seasonal amplitude arises from two major regions: the mid-latitude cropland between 256N and 606N and the high-latitude natural vegetation between 506N and 706 N. The long-term trend of seasonal amplitude increase is 0.311 ± 0.027 percent per year, of which sensitivity experiments attribute 45, 29 and 26 per cent to land-use change, climate variability and change, and increased productivity due to CO2 fertilization, respectively. Vegetation growth was earlier by one to two weeks, as measured by the mid-point of vegetation carbon uptake, and took up 0.5 petagrams more carbon in July, the height of the growing season, during 2001–2010 than in

  5. Calculating the balance between atmospheric CO2 drawdown and organic carbon oxidation in subglacial hydrochemical systems

    NASA Astrophysics Data System (ADS)

    Graly, Joseph A.; Drever, James I.; Humphrey, Neil F.

    2017-04-01

    In order to constrain CO2 fluxes from biogeochemical processes in subglacial environments, we model the evolution of pH and alkalinity over a range of subglacial weathering conditions. We show that subglacial waters reach or exceed atmospheric pCO2 levels when atmospheric gases are able to partially access the subglacial environment. Subsequently, closed system oxidation of sulfides is capable of producing pCO2 levels well in excess of atmosphere levels without any input from the decay of organic matter. We compared this model to published pH and alkalinity measurements from 21 glaciers and ice sheets. Most subglacial waters are near atmospheric pCO2 values. The assumption of an initial period of open system weathering requires substantial organic carbon oxidation in only 4 of the 21 analyzed ice bodies. If the subglacial environment is assumed to be closed from any input of atmospheric gas, large organic carbon inputs are required in nearly all cases. These closed system assumptions imply that order of 10 g m-2 y-1 of organic carbon are removed from a typical subglacial environment—a rate too high to represent soil carbon built up over previous interglacial periods and far in excess of fluxes of surface deposited organic carbon. Partial open system input of atmospheric gases is therefore likely in most subglacial environments. The decay of organic carbon is still important to subglacial inorganic chemistry where substantial reserves of ancient organic carbon are found in bedrock. In glaciers and ice sheets on silicate bedrock, substantial long-term drawdown of atmospheric CO2 occurs.

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

    PubMed

    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.

  7. Enhanced photosynthetic efficiency in trees world-wide by rising atmospheric CO2 levels

    NASA Astrophysics Data System (ADS)

    Ehlers, Ina; Wieloch, Thomas; Groenendijk, Peter; Vlam, Mart; van der Sleen, Peter; Zuidema, Pieter A.; Robertson, Iain; Schleucher, Jürgen

    2014-05-01

    The atmospheric CO2 concentration is increasing rapidly due to anthropogenic emissions but the effect on the Earth's biosphere is poorly understood. The ability of the biosphere to fix CO2 through photosynthesis will determine future atmospheric CO2 concentrations as well as future productivity of crops and forests. Manipulative CO2 enrichment experiments (e.g. FACE) are limited to (i) short time spans, (ii) few locations and (iii) large step increases in [CO2]. Here, we apply new stable isotope methodology to tree-ring archives, to study the effect of increasing CO2 concentrations retrospectively during the past centuries. We cover the whole [CO2] increase since industrialization, and sample trees with global distribution. Instead of isotope ratios of whole molecules, we use intramolecular isotope distributions, a new tool for tree-ring analysis with decisive advantages. In experiments on annual plants, we have found that the intramolecular distribution of deuterium (equivalent to ratios of isotopomer abundances) in photosynthetic glucose depends on growth [CO2] and reflects the metabolic flux ratio of photosynthesis to photorespiration. By applying this isotopomer methodology to trees from Oak Ridge FACE experiment, we show that this CO2 response is present in trees on the leaf level. This CO2 dependence constitutes a physiological signal, which is transferred to the wood of the tree rings. In trees from 13 locations on all continents the isotopomer ratio of tree-ring cellulose is correlated to atmospheric [CO2] during the past 200 years. The shift of the isotopomer ratio is universal for all 12 species analyzed, including both broad-leafed trees and conifers. Because the trees originate from sites with widely differing D/H ratios of precipitation, the generality of the response demonstrates that the signal is independent of the source isotope ratio, because it is encoded in an isotopomer abundance ratio. This decoupling of climate signals and physiological

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

    NASA Astrophysics Data System (ADS)

    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.

  9. Atmospheric effects on CO2 laser propagation

    NASA Technical Reports Server (NTRS)

    Murty, S. S. R.; Bilbro, J. W.

    1978-01-01

    An investigation was made of the losses encountered in the propagation of CO2 laser radiation through the atmosphere, particularly as it applies to the NASA/Marshall Space Flight Center Pulsed Laser Doppler System. As such it addresses three major areas associated with signal loss: molecular absorption, refractive index changes in a turbulent environment, and aerosol absorption and scattering. In particular, the molecular absorption coefficients of carbon dioxide, water vapor, and nitrous oxide are calculated for various laser lines in the region of 10.6 mu m as a function of various pressures and temperatures. The current status in the physics of low-energy laser propagation through a turbulent atmosphere is presented together with the analysis and evaluation of the associated heterodyne signal power loss. Finally, aerosol backscatter and extinction coefficients are calculated for various aerosol distributions and the results incorporated into the signal-to-noise ratio equation for the Marshall Space Flight Center system.

  10. Observations of Atmospheric Δ14CO2 at the Global and Regional Background Sites in China: Implication for Fossil Fuel CO2 Inputs.

    PubMed

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

    2016-11-15

    Six months to more than one year of atmospheric Δ 14 CO 2 were measured in 2014-2015 at one global background site in Waliguan (WLG) and four regional background sites at Shangdianzi (SDZ), Lin'an (LAN), Longfengshan (LFS) and Luhuitou (LHT), China. The objectives of the study are to document the Δ 14 CO 2 levels at each site and to trace the variations in fossil fuel CO 2 (CO 2ff ) inputs at regional background sites. Δ 14 CO 2 at WLG varied from 7.1 ± 2.9‰ to 32.0 ± 3.2‰ (average 17.1 ± 6.8‰) in 2015, with high values generally in autumn/summer and low values in winter/spring. During the same period, Δ 14 CO 2 values at the regional background sites were found to be significantly (p < 0.05) lower than those at WLG, indicating different levels of CO 2ff inputs at those sites. CO 2ff concentrations at LAN (12.7 ± 9.6 ppm) and SDZ (11.5 ± 8.2 ppm) were significantly (p < 0.05) higher than those at LHT (4.6 ± 4.3 ppm) in 2015. There were no significant (p > 0.05) seasonal differences in CO 2ff concentrations for the regional sites. Regional sources contributed in part to the CO 2ff inputs at LAN and SDZ, while local sources dominated the trend observed at LHT. These data provide a preliminary understanding of atmospheric Δ 14 CO 2 and CO 2ff inputs for a range of Chinese background sites.

  11. A 40-million-year history of atmospheric CO(2).

    PubMed

    Zhang, Yi Ge; Pagani, Mark; Liu, Zhonghui; Bohaty, Steven M; Deconto, Robert

    2013-10-28

    The alkenone-pCO2 methodology has been used to reconstruct the partial pressure of ancient atmospheric carbon dioxide (pCO2) for the past 45 million years of Earth's history (Middle Eocene to Pleistocene epochs). The present long-term CO2 record is a composite of data from multiple ocean localities that express a wide range of oceanographic and algal growth conditions that potentially bias CO2 results. In this study, we present a pCO2 record spanning the past 40 million years from a single marine locality, Ocean Drilling Program Site 925 located in the western equatorial Atlantic Ocean. The trends and absolute values of our new CO2 record site are broadly consistent with previously published multi-site alkenone-CO2 results. However, new pCO2 estimates for the Middle Miocene are notably higher than published records, with average pCO2 concentrations in the range of 400-500 ppm. Our results are generally consistent with recent pCO2 estimates based on boron isotope-pH data and stomatal index records, and suggest that CO2 levels were highest during a period of global warmth associated with the Middle Miocene Climatic Optimum (17-14 million years ago, Ma), followed by a decline in CO2 during the Middle Miocene Climate Transition (approx. 14 Ma). Several relationships remain contrary to expectations. For example, benthic foraminiferal δ(18)O records suggest a period of deglaciation and/or high-latitude warming during the latest Oligocene (27-23 Ma) that, based on our results, occurred concurrently with a long-term decrease in CO2 levels. Additionally, a large positive δ(18)O excursion near the Oligocene-Miocene boundary (the Mi-1 event, approx. 23 Ma), assumed to represent a period of glacial advance and retreat on Antarctica, is difficult to explain by our CO2 record alone given what is known of Antarctic ice sheet history and the strong hysteresis of the East Antarctic Ice Sheet once it has grown to continental dimensions. We also demonstrate that in the

  12. Investigating the role of evergreen and deciduous forests in the increasing trend in atmospheric CO2 seasonal amplitude

    NASA Astrophysics Data System (ADS)

    Welp, L.; Calle, L.; Graven, H. D.; Poulter, B.

    2017-12-01

    The seasonal amplitude of Northern Hemisphere atmospheric CO2 concentrations has systematically increased over the last several decades, indicating that the timing and amplitude of net CO2 uptake and release by northern terrestrial ecosystems has changed substantially. Remote sensing, dynamic vegetation modeling, and in-situ studies have explored how changes in phenology, expansion of woody vegetation, and changes in species composition and disturbance regimes, among others, are driven by changes in climate and CO2. Despite these efforts, ecosystem models have not been able to reproduce observed atmospheric CO2 changes. Furthermore, the implications for the source/sink balance of northern ecosystems remains unclear. Changing proportions of evergreen and deciduous tree cover in response to climate change could be one of the key mechanisms that have given rise to amplified atmospheric CO2 seasonality. These two different plant functional types (PFTs) have different carbon uptake seasonal patterns and also different sensitivities to climate change, but are often lumped together as one forest type in global ecosystem models. We will demonstrate the potential that shifting distributions of evergreen and deciduous forests can have on the amplitude of atmospheric CO2. We will show phase differences in the net CO2 seasonal uptake using CO2 flux data from paired evergreen/deciduous eddy covariance towers. We will use simulations of evergreen and deciduous PFTs from the LPJ dynamic vegetation model to explore how climate change may influence the abundance and CO2 fluxes of each. Model results show that the area of deciduous forests is predicted to have increased, and the seasonal amplitude of CO2 fluxes has increased as well. The impact of surface flux seasonal variability on atmospheric CO2 amplitude is examined by transporting fluxes from each forest PFT through the TM3 transport model. The timing of the most intense CO2 uptake leads to an enhanced effect of deciduous

  13. Nannofossil carbonate fluxes during the Early Cretaceous: Phytoplankton response to nutrification episodes, atmospheric CO2, and anoxia

    NASA Astrophysics Data System (ADS)

    Erba, Elisabetta; Tremolada, Fabrizio

    2004-03-01

    Greenhouse episodes during the Valanginian and Aptian correlate with major perturbations in the C cycle and in marine ecosystems, carbonate crises, and widespread deposition of Corg-rich black shales. Quantitative analyses of nannofossil micrite were conducted on continuous pelagic sections from the Southern Alps (northern Italy), where high-resolution integrated stratigraphy allows precise dating of Early Cretaceous geological events. Rock-forming calcareous nannofloras were quantified in smear slides and thin sections to obtain relative and absolute abundances and paleofluxes that are interpreted as the response of calcareous phytoplankton to global changes in the ocean-atmosphere system. Increased rates of volcanism during the formation of Ontong Java and Manihiki Plateaus and the Paranà-Etendeka large igneous province (LIP) are proposed to have caused the geological responses associated with early Aptian oceanic anoxic event (OAE) 1a and the Valanginian event, respectively. Calcareous nannofloras reacted to the new conditions of higher pCO2 and fertility by drastically reducing calcification. The Valanginian event is marked by a 65% reduction in nannofossil paleofluxes that would correspond to a 2-3 times increase in pCO2 during formation of the Paranà-Endenteka LIP. A 90% reduction in nannofossil paleofluxes, which occurred in a 1.5 myr-long interval leading into OAE1a, is interpreted as the result of a 3-6 times increase in pCO2 produced by emplacement of the giant Ontong Java and Manihiki Plateaus. High pCO2 was balanced back by an accelerated biological pump during the Valanginian episode, but not during OAE1a, suggesting persisting high levels of pCO2 in the late Aptian and/or the inability of calcareous phytoplankton to absorb excess pCO2 above threshold values.

  14. Soil organic carbon dust emission: an omitted global source of atmospheric CO2.

    PubMed

    Chappell, Adrian; Webb, Nicholas P; Butler, Harry J; Strong, Craig L; McTainsh, Grant H; Leys, John F; Viscarra Rossel, Raphael A

    2013-10-01

    Soil erosion redistributes soil organic carbon (SOC) within terrestrial ecosystems, to the atmosphere and oceans. Dust export is an essential component of the carbon (C) and carbon dioxide (CO(2)) budget because wind erosion contributes to the C cycle by removing selectively SOC from vast areas and transporting C dust quickly offshore; augmenting the net loss of C from terrestrial systems. However, the contribution of wind erosion to rates of C release and sequestration is poorly understood. Here, we describe how SOC dust emission is omitted from national C accounting, is an underestimated source of CO(2) and may accelerate SOC decomposition. Similarly, long dust residence times in the unshielded atmospheric environment may considerably increase CO(2) emission. We developed a first approximation to SOC enrichment for a well-established dust emission model and quantified SOC dust emission for Australia (5.83 Tg CO(2)-e yr(-1)) and Australian agricultural soils (0.4 Tg CO(2)-e yr(-1)). These amount to underestimates for CO(2) emissions of ≈10% from combined C pools in Australia (year = 2000), ≈5% from Australian Rangelands and ≈3% of Australian Agricultural Soils by Kyoto Accounting. Northern hemisphere countries with greater dust emission than Australia are also likely to have much larger SOC dust emission. Therefore, omission of SOC dust emission likely represents a considerable underestimate from those nations' C accounts. We suggest that the omission of SOC dust emission from C cycling and C accounting is a significant global source of uncertainty. Tracing the fate of wind-eroded SOC in the dust cycle is therefore essential to quantify the release of CO(2) from SOC dust to the atmosphere and the contribution of SOC deposition to downwind C sinks. © 2013 John Wiley & Sons Ltd.

  15. Can the envisaged reductions of fossil fuel CO2 emissions be detected by atmospheric observations?

    PubMed

    Levin, Ingeborg; Rödenbeck, Christian

    2008-03-01

    The lower troposphere is an excellent receptacle, which integrates anthropogenic greenhouse gases emissions over large areas. Therefore, atmospheric concentration observations over populated regions would provide the ultimate proof if sustained emissions changes have occurred. The most important anthropogenic greenhouse gas, carbon dioxide (CO(2)), also shows large natural concentration variations, which need to be disentangled from anthropogenic signals to assess changes in associated emissions. This is in principle possible for the fossil fuel CO(2) component (FFCO(2)) by high-precision radiocarbon ((14)C) analyses because FFCO(2) is free of radiocarbon. Long-term observations of (14)CO(2) conducted at two sites in south-western Germany do not yet reveal any significant trends in the regional fossil fuel CO(2) component. We rather observe strong inter-annual variations, which are largely imprinted by changes of atmospheric transport as supported by dedicated transport model simulations of fossil fuel CO(2). In this paper, we show that, depending on the remoteness of the site, changes of about 7-26% in fossil fuel emissions in respective catchment areas could be detected with confidence by high-precision atmospheric (14)CO(2) measurements when comparing 5-year averages if these inter-annual variations were taken into account. This perspective constitutes the urgently needed tool for validation of fossil fuel CO(2) emissions changes in the framework of the Kyoto protocol and successive climate initiatives.

  16. Low atmospheric CO(2) levels during the Permo- Carboniferous glaciation inferred from fossil lycopsids.

    PubMed

    Beerling, D J

    2002-10-01

    Earth history was punctuated during the Permo-Carboniferous [300-250 million years (Myr) ago] by the longest and most severe glaciation of the entire Phanerozoic Eon. But significant uncertainty surrounds the concentration of CO(2) in the atmosphere through this time interval and therefore its role in the evolution of this major prePleistocene glaciation. Here, I derive 24 Late Paleozoic CO(2) estimates from the fossil cuticle record of arborsecent lycopsids of the equatorial Carboniferous and Permian swamp communities. Quantitative calibration of Late Carboniferous (330-300 Myr ago) and Permian (270-260 Myr ago) lycopsid stomatal indices yield average atmospheric CO(2) concentrations of 344 ppm and 313 ppm, respectively. The reconstructions show a high degree of self-consistency and a degree of precision an order of magnitude greater than other approaches. Low CO(2) levels during the Permo-Carboniferous glaciation are in agreement with glaciological evidence for the presence of continental ice and coupled models of climate and ice-sheet growth on Pangea. Moreover, the Permian data indicate atmospheric CO(2) levels were low 260 Myr ago, by which time continental deglaciation was already underway. Positive biotic feedbacks on climate, and geotectonic events, therefore are implicated as mechanisms underlying deglaciation.

  17. Low atmospheric CO2 levels during the Permo- Carboniferous glaciation inferred from fossil lycopsids

    PubMed Central

    Beerling, D. J.

    2002-01-01

    Earth history was punctuated during the Permo-Carboniferous [300–250 million years (Myr) ago] by the longest and most severe glaciation of the entire Phanerozoic Eon. But significant uncertainty surrounds the concentration of CO2 in the atmosphere through this time interval and therefore its role in the evolution of this major prePleistocene glaciation. Here, I derive 24 Late Paleozoic CO2 estimates from the fossil cuticle record of arborsecent lycopsids of the equatorial Carboniferous and Permian swamp communities. Quantitative calibration of Late Carboniferous (330–300 Myr ago) and Permian (270–260 Myr ago) lycopsid stomatal indices yield average atmospheric CO2 concentrations of 344 ppm and 313 ppm, respectively. The reconstructions show a high degree of self-consistency and a degree of precision an order of magnitude greater than other approaches. Low CO2 levels during the Permo-Carboniferous glaciation are in agreement with glaciological evidence for the presence of continental ice and coupled models of climate and ice-sheet growth on Pangea. Moreover, the Permian data indicate atmospheric CO2 levels were low 260 Myr ago, by which time continental deglaciation was already underway. Positive biotic feedbacks on climate, and geotectonic events, therefore are implicated as mechanisms underlying deglaciation. PMID:12235372

  18. Enhanced microwave absorbing performance of CoNi alloy nanoparticles anchored on a spherical carbon monolith.

    PubMed

    Li, Na; Hu, Changwen; Cao, Minhua

    2013-05-28

    CoNi alloy nanoparticles anchored on a spherical carbon monolith (CoNi-C) were prepared by a solvothermal route and subsequent heat treatment without any templates. Their permittivity and permeability behaviors were studied in the frequency range of 2-18 GHz. The CoNi-C composites showed the best microwave absorbing performances compared to those of Co-C and Ni-C. The maximum reflection loss of the CoNi-C nanocomposites can reach -50.2 dB at 7.7 GHz with samples of 4 mm in thickness, better than that of the Ni-C composites, while the Co-C composites showed almost no absorption at all. The absorption mechanism of the three absorbents was also discussed.

  19. Increasing atmospheric CO2 reduces metabolic and physiological differences between isoprene- and non-isoprene-emitting poplars.

    PubMed

    Way, Danielle A; Ghirardo, Andrea; Kanawati, Basem; Esperschütz, Jürgen; Monson, Russell K; Jackson, Robert B; Schmitt-Kopplin, Philippe; Schnitzler, Jörg-Peter

    2013-10-01

    Isoprene, a volatile organic compound produced by some plant species, enhances abiotic stress tolerance under current atmospheric CO2 concentrations, but its biosynthesis is negatively correlated with CO2 concentrations. We hypothesized that losing the capacity to produce isoprene would require stronger up-regulation of other stress tolerance mechanisms at low CO2 than at higher CO2 concentrations. We compared metabolite profiles and physiological performance in poplars (Populus × canescens) with either wild-type or RNAi-suppressed isoprene emission capacity grown at pre-industrial low, current atmospheric, and future high CO2 concentrations (190, 390 and 590 ppm CO2 , respectively). Suppression of isoprene biosynthesis led to significant rearrangement of the leaf metabolome, increasing stress tolerance responses such as xanthophyll cycle pigment de-epoxidation and antioxidant levels, as well as altering lipid, carbon and nitrogen metabolism. Metabolic and physiological differences between isoprene-emitting and suppressed lines diminished as growth CO2 concentrations rose. The CO2 dependence of our results indicates that the effects of isoprene biosynthesis are strongest at pre-industrial CO2 concentrations. Rising CO2 may reduce the beneficial effects of biogenic isoprene emission, with implications for species competition. This has potential consequences for future climate warming, as isoprene emitted from vegetation has strong effects on global atmospheric chemistry. © 2013 The Authors. New Phytologist © 2013 New Phytologist Trust.

  20. Modeling the volcanic signal in the atmospheric CO2 record

    NASA Astrophysics Data System (ADS)

    Jones, Chris D.; Cox, Peter M.

    2001-06-01

    There is significant interannual variability in the atmospheric concentration of carbon dioxide even when the effect of anthropogenic sources has been accounted for. It has been shown that this variability is correlated with the El Nino Southern Oscillation (ENSO) cycle [Bacastow, 1976; Keeling et al., 1995]. However, there are periods during the atmospheric CO2 record when this correlation does not hold and CO2 levels are much lower than can be explained by the correlation with ENSO. These periods coincide with major volcanic eruptions. It has been well documented that a major eruption has a cooling effect on the surface and lower troposphere [McCormick, 1992; Hansen, et al., 1996]. Here we show that it is likely that this cooling has a significant and measurable effect on the carbon cycle. We use a coupled general circulation climate-carbon cycle model to study the mechanisms involved. The model simulates the observed temperature and CO2 response of the climate to the 1991 eruption of Mount Pinatubo. The surface cooling due to the eruption leads to reduced soil and plant respiration globally and increased gross primary productivity in the tropics. The result is significant uptake of carbon (1-2 GtC yr-1) by the terrestrial biosphere for several years after the eruption. There is no significant variation in uptake or release of carbon by the oceans.

  1. Soil CO2 flux in response to elevated atmospheric CO2 and nitrogen fertilization: patterns and methods

    Treesearch

    James M. Vose; Katherine J. Elliott; D.W. Johnson

    1995-01-01

    The evolution of carbon dioxide (CO2) from soils is due to the metabolic activity of roots, mycorrhizae, and soil micro- and macro-organisms. Although precise estimates of carbon (C) recycled to the atmosphere from belowground sources are unavailable, Musselman and Fox (1991) propose that the belowground contribution exceeds 100 Pg y-1...

  2. Mixing ratio and carbon isotopic composition investigation of atmospheric CO2 in Beijing, China.

    PubMed

    Pang, Jiaping; Wen, Xuefa; Sun, Xiaomin

    2016-01-01

    The stable isotope composition of atmospheric CO2 can be used as a tracer in the study of urban carbon cycles, which are affected by anthropogenic and biogenic CO2 components. Continuous measurements of the mixing ratio and δ(13)C of atmospheric CO2 were conducted in Beijing from Nov. 15, 2012 to Mar. 8, 2014 including two heating seasons and a vegetative season. Both δ(13)C and the isotopic composition of source CO2 (δ(13)CS) were depleted in the heating seasons and enriched in the vegetative season. The diurnal variations in the CO2 mixing ratio and δ(13)C contained two peaks in the heating season, which are due to the effects of morning rush hour traffic. Seasonal and diurnal patterns of the CO2 mixing ratio and δ(13)C were affected by anthropogenic emissions and biogenic activity. Assuming that the primary CO2 sources at night (22:00-04:00) were coal and natural gas combustion during heating seasons I and II, an isotopic mass balance analysis indicated that coal combustion had average contributions of 83.83±14.11% and 86.84±12.27% and that natural gas had average contributions of 16.17±14.11% and 13.16±12.27%, respectively. The δ(13)C of background CO2 in air was the main error source in the isotopic mass balance model. Both the mixing ratio and δ(13)C of atmospheric CO2 had significant linear relationships with the air quality index (AQI) and can be used to indicate local air pollution conditions. Energy structure optimization, for example, reducing coal consumption, will improve the local air conditions in Beijing. Copyright © 2015 Elsevier B.V. All rights reserved.

  3. Mixing ratio and carbon isotopic composition investigation of atmospheric CO2 in Beijing, China

    NASA Astrophysics Data System (ADS)

    Pang, J.; Wen, X.; Sun, X.

    2016-12-01

    The stable isotope composition of atmospheric CO2 can be used as a tracer in the study of urban carbon cycles, which are affected by anthropogenic and biogenic CO2 components. Continuous measurements of the mixing ratio and δ13C of atmospheric CO2 were conducted in Beijing from Nov. 15, 2012 to Mar. 8, 2014 including two heating seasons and a vegetative season. Both δ13C and the isotopic composition of source CO2 (δ13CS) were depleted in the heating seasons and enriched in the vegetative season. The diurnal variations in the CO2 mixing ratio and δ13C contained two peaks in the heating season, which are due to the effects of morning rush hour traffic. Seasonal and diurnal patterns of the CO2 mixing ratio and δ13C were affected by anthropogenic emissions and biogenic activity. Assuming that the primary CO2 sources at night (22:00-04:00) were coal and natural gas combustion during heating seasons I and II, an isotopic mass balance analysis indicated that coal combustion had average contributions of 83.83 ± 14.11% and 86.84 ± 12.27% and that natural gas had average contributions of 16.17 ± 14.11% and 13.16 ± 12.27%, respectively. The δ13C of background CO2 in air was the main error source in the isotopic mass balance model. Both the mixing ratio and δ13C of atmospheric CO2 had significant linear relationships with the air quality index (AQI) and can be used to indicate local air pollution conditions. Energy structure optimization, for example, reducing coal consumption, will improve the local air conditions in Beijing.

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

    PubMed

    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.

  5. Simultaneous Measurements of CO2 Concentration and Temperature profiles using 1.6 μm DIAL in the Lower-Atmosphere

    NASA Astrophysics Data System (ADS)

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

    2016-12-01

    High-accurate vertical carbon dioxide (CO2) profiles are highly desirable in the inverse method to improve quantification and understanding of the global sink and source of CO2, and also global climate change. We have developed a ground based 1.6μm differential absorption lidar (DIAL) to achieve measurements of vertical CO2 profiles in the atmosphere. As the spectra of absorption lines of any molecules are influenced basically by the temperature and pressure in the atmosphere, it is important to measure them simultaneously so that the better accuracy of the DIAL measurement is realized. The barometric formula can derive atmospheric pressure of each altitude using atmospheric pressure of ground level at the lidar site. Comparison of atmospheric pressure prlofiles calculated from this equation and those obtained from radiosonde observations at Tateno, Japan are consisted within 0.2 % below 3 km altitude. So, we have developed a 1.6 μm CO2 DIAL system for simultaneous measurements of the CO2 concentration and temperature profiles in the lower-atmosphere. Laser beams of three wavelengths around a CO2 absorption spectrum is transmitted alternately to the atmosphere. Moreover, the value of the retrieved CO2 concentration will be improved remarkably by processing the iteration assignment of CO2 concentration and temperature, which measured by these DIAL techniques. We have acheived vertical CO2 concentration and temperature profile from 0.5 to 2.0 km altitude by this DIAL system. In the next step, we will use this high accuracy CO2 concentration profile and back-trajectory analysis for the behavior analysis of the CO2 mass. This work was financially supported by the System Development Program for Advanced Measurement and Analysis of the Japan Science and Technology Agency.

  6. New Approaches to Quantifying Transport Model Error in Atmospheric CO2 Simulations

    NASA Technical Reports Server (NTRS)

    Ott, L.; Pawson, S.; Zhu, Z.; Nielsen, J. E.; Collatz, G. J.; Gregg, W. W.

    2012-01-01

    In recent years, much progress has been made in observing CO2 distributions from space. However, the use of these observations to infer source/sink distributions in inversion studies continues to be complicated by difficulty in quantifying atmospheric transport model errors. We will present results from several different experiments designed to quantify different aspects of transport error using the Goddard Earth Observing System, Version 5 (GEOS-5) Atmospheric General Circulation Model (AGCM). In the first set of experiments, an ensemble of simulations is constructed using perturbations to parameters in the model s moist physics and turbulence parameterizations that control sub-grid scale transport of trace gases. Analysis of the ensemble spread and scales of temporal and spatial variability among the simulations allows insight into how parameterized, small-scale transport processes influence simulated CO2 distributions. In the second set of experiments, atmospheric tracers representing model error are constructed using observation minus analysis statistics from NASA's Modern-Era Retrospective Analysis for Research and Applications (MERRA). The goal of these simulations is to understand how errors in large scale dynamics are distributed, and how they propagate in space and time, affecting trace gas distributions. These simulations will also be compared to results from NASA's Carbon Monitoring System Flux Pilot Project that quantified the impact of uncertainty in satellite constrained CO2 flux estimates on atmospheric mixing ratios to assess the major factors governing uncertainty in global and regional trace gas distributions.

  7. Role of advection for the ecosystem-atmosphere CO2 exchange of alpine grasslands

    NASA Astrophysics Data System (ADS)

    Zhao, Peng; Wohlfahrt, Georg

    2017-04-01

    The neglect of the advection contribution could bring uncertainties to the estimation of the net ecosystem CO2 exchange (NEE) between ecosystems and the atmosphere, especially in complex terrain and stable atmospheric conditions. In order to quantify the advection flux of CO2, we carried out four monthly field campaigns at different grasslands in the mountainous areas of Italy, Austria, and Germany in 2015 and 2016. The measurement was based on the advection completed mass balance (ACMB) concept. A home-assembled solenoid valve system, together with multiple sampling inlets and a gas analyser, was used to measure CO2 concentration online at three heights on the four sides of a control volume of 20 m by 20 m. Advection of CO2 was then calculated from the measurement of wind components and CO2 gradients. The turbulent flux of CO2 was measured by the eddy-covariance technique. Three clear automatic chambers measured NEE as reference. Results showed that both the horizontal and vertical advection contributed more significantly to CO2 flux at night time than at daytime. At most sites, the horizontal advection played a more important role than the vertical advection. The above-canopy advection contributed more CO2 flux than within-canopy advection due to the short canopy heights. Large variability of NEE measured by the three chambers indicates the challenge of comparing chamber and micrometeorological fluxes resulting from the heterogeneity of the surface.

  8. Radiative transfer in CO2-rich atmospheres: 1. Collisional line mixing implies a colder early Mars

    NASA Astrophysics Data System (ADS)

    Ozak, N.; Aharonson, O.; Halevy, I.

    2016-06-01

    Fast and accurate radiative transfer methods are essential for modeling CO2-rich atmospheres, relevant to the climate of early Earth and Mars, present-day Venus, and some exoplanets. Although such models already exist, their accuracy may be improved as better theoretical and experimental constraints become available. Here we develop a unidimensional radiative transfer code for CO2-rich atmospheres, using the correlated k approach and with a focus on modeling early Mars. Our model differs from existing models in that it includes the effects of CO2 collisional line mixing in the calculation of the line-by-line absorption coefficients. Inclusion of these effects results in model atmospheres that are more transparent to infrared radiation and, therefore, in colder surface temperatures at radiative-convective equilibrium, compared with results of previous studies. Inclusion of water vapor in the model atmosphere results in negligible warming due to the low atmospheric temperatures under a weaker early Sun, which translate into climatically unimportant concentrations of water vapor. Overall, the results imply that sustained warmth on early Mars would not have been possible with an atmosphere containing only CO2 and water vapor, suggesting that other components of the early Martian climate system are missing from current models or that warm conditions were not long lived.

  9. Earth 2075 (CO2) - can Ocean-Amplified Carbon Capture (oacc) Impart Atmospheric CO2-SINKING Ability to CCS Fossil Energy?

    NASA Astrophysics Data System (ADS)

    Fry, R.; Routh, M.; Chaudhuri, S.; Fry, S.; Ison, M.; Hughes, S.; Komor, C.; Klabunde, K.; Sethi, V.; Collins, D.; Polkinghorn, W.; Wroobel, B.; Hughes, J.; Gower, G.; Shkolnik, J.

    2017-12-01

    Previous attempts to capture atmospheric CO2 by algal blooming were stalled by ocean viruses, zooplankton feeding, and/or bacterial decomposition of surface blooms, re-releasing captured CO2 instead of exporting it to seafloor. CCS fossil energy coupling could bypass algal bloom limits—enabling capture of 10 GtC/yr atmospheric CO2 by selective emiliania huxleyi (EHUX) blooming in mid-latitude open oceans, far from coastal waters and polar seas. This could enable a 500 GtC drawdown, 350 ppm restoration by 2050, 280 ppm CO2 by 2075, and ocean pH 8.2. White EHUX blooms could also reflect sunlight back into outer space and seed extra ocean cloud cover, via DMS release, to raise albedo 1.8%—restoring preindustrial temperature (ΔT = 0°C) by 2030. Open oceans would avoid post-bloom anoxia, exclusively a coastal water phenomenon. The EHUX calcification reaction initially sources CO2, but net sinking prevails in follow-up equilibration reactions. Heavier-than-water EHUX sink captured CO2 to the sea floor before surface decomposition occurs. Seeding EHUX high on their nonlinear growth curve could accelerate short-cycle secondary open-ocean blooming—overwhelming mid-latitude viruses, zooplankton, and competition from other algae. Mid-latitude "ocean deserts" exhibit low viral, zooplankton, and bacterial counts. Thermocline prevents nutrient upwelling that would otherwise promote competing algae. Adding nitrogen nutrient would foster exclusive EHUX blooming. Elevated EHUX seed levels could arise from sealed, pH-buffered, floating, seed-production bioreactors infused with 10% CO2 from carbon feedstock supplied by inland CCS fossil power plants capturing 90% of emissions as liquid CO2. Deep-water SPAR platforms extract natural gas from beneath the sea floor. On-platform Haber and pH processing could convert extracted CH4 to buffered NH4+ nutrient, enabling ≥0.7 GtC/yr of bioreactor seed production and 10 GtC/yr of amplified secondary open-ocean CO2 capture—making CCS

  10. Effects of elevated atmospheric CO2 and N fertilization on bahiagrass root distribution

    USDA-ARS?s Scientific Manuscript database

    The effects of elevated atmospheric CO2 on pasture systems remain understudied in the Southeastern US. A 10-year study of bahiagrass (Paspalum notatum Flüggé) response to elevated CO2 was established in 2005 using open top field chambers on a Blanton loamy sand (loamy siliceous, thermic, Grossarenic...

  11. Thermodynamics and kinetics parameters of co-combustion between sewage sludge and water hyacinth in CO2/O2 atmosphere as biomass to solid biofuel.

    PubMed

    Huang, Limao; Liu, Jingyong; He, Yao; Sun, Shuiyu; Chen, Jiacong; Sun, Jian; Chang, KenLin; Kuo, Jiahong; Ning, Xun'an

    2016-10-01

    Thermodynamics and kinetics of sewage sludge (SS) and water hyacinth (WH) co-combustion as a blend fuel (SW) for bioenergy production were studied through thermogravimetric analysis. In CO2/O2 atmosphere, the combustion performance of SS added with 10-40wt.% WH was improved 1-1.97 times as revealed by the comprehensive combustion characteristic index (CCI). The conversion of SW in different atmospheres was identified and their thermodynamic parameters (ΔH,ΔS,ΔG) were obtained. As the oxygen concentration increased from 20% to 70%, the ignition temperature of SW decreased from 243.1°C to 240.3°C, and the maximum weight loss rate and CCI increased from 5.70%·min(-1) to 7.26%·min(-1) and from 4.913%(2)·K(-3)·min(-2) to 6.327%(2)·K(-3)·min(-2), respectively, which corresponded to the variation in ΔS and ΔG. The lowest activation energy (Ea) of SW was obtained in CO2/O2=7/3 atmosphere. Copyright © 2016 Elsevier Ltd. All rights reserved.

  12. Does Silicate Weathering of Loess Affect Atmospheric CO2?

    NASA Astrophysics Data System (ADS)

    Anderson, S. P.

    2002-12-01

    Weathering of glacial loess may be a significant, yet unrecognized, component of the carbon cycle. Glaciers produce fine-grained sediment, exposing vast amounts of mineral surface area to weathering processes, yet silicate mineral weathering rates at glacier beds and of glacial till are not high. Thus, despite the tremendous potential for glaciers to influence global weathering rates and atmospheric CO2 levels, this effect has not been demonstrated. Loess, comprised of silt-clay sizes, may be the key glacial deposit in which silicate weathering rates are high. Loess is transported by wind off braid plains of rivers, and deposited broadly (order 100 km from the source) in vegetated areas. Both the fine grain size, and hence large mineral surface area, and presence of vegetation should render loess deposits highly susceptible to silicate weathering. These deposits effectively extend the geochemical impact of glaciation in time and space, and bring rock flour into conditions conducive to chemical weathering. A simple 1-d model of silicate weathering fluxes from a soil profile demonstrates the potential of loess deposition to enhance CO2 consumption. At each time step, computed mineral dissolution (using anorthite and field-based rate constants) modifies the size of mineral grains within the soil. In the case of a stable soil surface, this results in a gradual decline in weathering fluxes and CO2 consumption through time, as finer grain sizes dissolve away. Computed weathering fluxes for a typical loess, with an initial mean grain size of 25 μm, are an order of magnitude greater than fluxes from a non-loess soil that differs only in having a mean grain size of 320 μm. High weathering fluxes are maintained through time if loess is continually deposited. Deposition rates as low as 0.01 mm/yr (one loess grain thickness per year) can lead to a doubling of CO2 consumption rates within 5 ka. These results suggest that even modest loess deposition rates can significantly

  13. The Role of Artificial Atmospheric CO2 Removal in Stabilizing Earth's Climate

    NASA Astrophysics Data System (ADS)

    Tokarska, Katarzyna; Zickfeld, Kirsten

    2014-05-01

    Recent research showed that global mean temperature remains approximately constant for several centuries after complete cessation of CO2 emissions, while global mean thermosteric sea level continues to rise. This implies that a net artificial removal of CO2 from the atmosphere may be necessary to decrease the atmospheric CO2 concentrations more rapidly and bring the climate system components to their previous states on human timescales. The purpose of this study is to explore the reversibility of climate responses to a range of realistic CO2 emission scenarios, which follow a gradual transition from fossil-fuel driven economy to a zero-emission energy system with implementation of negative CO2 emissions, using the University of Victoria Earth System Climate Model of intermediate complexity (UVic ESCM 2.9). The CO2 emission pathways were designed to meet constraints related to the implementation of negative emission technologies derived from the integrated assessment literature. Our simulations show that while it is possible, in principle, to revert the global mean temperature after a phase of overshoot, the thermosteric sea level rise is not reversible on human timescales for the range of emission scenarios considered. During the negative emission phase, CO2 is released form the natural (terrestrial and marine) carbon sinks, which diminishes the efficiency of negative emissions implemented. In addition, spatial changes of vegetation distribution patterns are not entirely reversible on human timescales. We suggest that while negative emissions could potentially stabilize the global mean temperature at a desired level, such technology does not supersede reductions in fossil fuel emissions, as the artificial CO2 capture at large scale has many limitations and is unable to stabilize other climate system components (e.g. sea level) at desired levels.

  14. An Atmospheric CO2 Record Across the End-Cretaceous Extinction

    NASA Astrophysics Data System (ADS)

    Royer, D. L.; Milligan, J. N.; Kowalczyk, J.

    2017-12-01

    A bolide impact and flood-basalt emissions likely caused large changes to the end-Cretaceous carbon cycle. Presently, there is only one proxy record for atmospheric CO2 that captures these changes (Beerling et al., 2002, PNAS 99: 7836-7840). These authors estimated CO2 from the calibrated stomatal indices of Ginkgo dated to within 105 yrs before and after the extinction ( 300-500 ppm) in addition to that of Stenochlaena, a fern disaster taxa present in the Raton Basin, New Mexico, <104 yrs after the bolide impact (>2300 ppm). We revisited these fossil collections and applied a newer and more robust CO2 proxy that is based on leaf gas-exchange principles and does not require calibrations with present-day species (Franks et al., 2014, Geophys Res Lett 41: 4685-4694). We reconstruct pre- and post-extinction CO2 concentrations of 650 ppm from Ginkgo, compared to 850 ppm directly after the extinction from Stenochlaena. This change in CO2 of 200 ppm can be readily explained with carbon cycle models as a consequence of either the bolide impact or flood-basalt emissions. Placing these CO2 estimates into the broader context of other leaf gas-exchange CO2 estimates for the Cenozoic, the Earth system sensitivity was 3 K per CO2 doubling during the early Paleogene, before steepening to >6 K several million years before the Eocene-Oligocene boundary.

  15. Influence of El Niño on atmospheric CO2 over the tropical Pacific Ocean: Findings from NASA's OCO-2 mission.

    PubMed

    Chatterjee, A; Gierach, M M; Sutton, A J; Feely, R A; Crisp, D; Eldering, A; Gunson, M R; O'Dell, C W; Stephens, B B; Schimel, D S

    2017-10-13

    Spaceborne observations of carbon dioxide (CO 2 ) from the Orbiting Carbon Observatory-2 are used to characterize the response of tropical atmospheric CO 2 concentrations to the strong El Niño event of 2015-2016. Although correlations between the growth rate of atmospheric CO 2 concentrations and the El Niño-Southern Oscillation are well known, the magnitude of the correlation and the timing of the responses of oceanic and terrestrial carbon cycle remain poorly constrained in space and time. We used space-based CO 2 observations to confirm that the tropical Pacific Ocean does play an early and important role in modulating the changes in atmospheric CO 2 concentrations during El Niño events-a phenomenon inferred but not previously observed because of insufficient high-density, broad-scale CO 2 observations over the tropics. Copyright © 2017 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works.

  16. What would optimal vegetation do when confronted with steadily increasing atmospheric CO2

    NASA Astrophysics Data System (ADS)

    Roderick, M. L.; Donohue, R. J.; Yang, Y.; McVicar, T.; Farquhar, G. D.

    2015-12-01

    The ongoing increase in atmospheric CO2 presents an interesting opportunity for primary producers. An increase in the substrate availability would, with all else equal, stimulate fixation of carbon from the atmosphere. But all else is not necessarily equal and this is only the beginning of a cascade of changes that can ultimately be traced back to the stomatal regulation of water-carbon exchanges. We first discuss theoretical expectations and then deduce how vegetation might respond to changing CO2 in water- and energy-limited environments. We then use satellite observations to test the theoretical expectations.

  17. Will elevated atmospheric CO2 boost the growth of an invasive submerged macrophyte Cabomba caroliniana under the interference of phytoplankton?

    PubMed

    Liu, Xin; Han, Yanqing; Zhu, Jinge; Deng, Jiancai; Hu, Weiping; da Silva, Thomaz Edson Veloso

    2018-01-01

    The growth of most submerged macrophytes is likely to be limited by the availability of carbon resource, and this is especially true for the obligatory carbon dioxide (CO 2 ) users. A mesocosm experiment was performed to investigate the physiological, photophysiological, and biochemical responses of Cabomba caroliniana, an invasive macrophyte specie in the Lake Taihu Basin, to elevated atmospheric CO 2 (1000 μmol mol -1 ); we also examined the possible impacts of interferences derived from the phytoplankton proliferation and its concomitant disturbances on the growth of C. caroliniana. The results demonstrated that elevated atmospheric CO 2 significantly enhanced the biomass, relative growth rate, and photosynthate accumulation of C. caroliniana. C. caroliniana exposed to elevated atmospheric CO 2 exhibited a higher relative maximum electron transport rate and photosynthetic efficiency, compared to those exposed to ambient atmospheric CO 2 . However, the positive effects of elevated atmospheric CO 2 on C. caroliniana were gradually compromised as time went by, and the down-regulations of the relative growth rate (RGR) and photosynthetic activity were coupled with phytoplankton proliferation under elevated atmospheric CO 2 . This study demonstrated that the growth of C. caroliniana under the phytoplankton interference can be greatly affected, directly and indirectly, by the increasing atmospheric CO 2 .

  18. Faster turnover of new soil carbon inputs under increased atmospheric CO2.

    PubMed

    van Groenigen, Kees Jan; Osenberg, Craig W; Terrer, César; Carrillo, Yolima; Dijkstra, Feike A; Heath, James; Nie, Ming; Pendall, Elise; Phillips, Richard P; Hungate, Bruce A

    2017-10-01

    Rising levels of atmospheric CO 2 frequently stimulate plant inputs to soil, but the consequences of these changes for soil carbon (C) dynamics are poorly understood. Plant-derived inputs can accumulate in the soil and become part of the soil C pool ("new soil C"), or accelerate losses of pre-existing ("old") soil C. The dynamics of the new and old pools will likely differ and alter the long-term fate of soil C, but these separate pools, which can be distinguished through isotopic labeling, have not been considered in past syntheses. Using meta-analysis, we found that while elevated CO 2 (ranging from 550 to 800 parts per million by volume) stimulates the accumulation of new soil C in the short term (<1 year), these effects do not persist in the longer term (1-4 years). Elevated CO 2 does not affect the decomposition or the size of the old soil C pool over either temporal scale. Our results are inconsistent with predictions of conventional soil C models and suggest that elevated CO 2 might increase turnover rates of new soil C. Because increased turnover rates of new soil C limit the potential for additional soil C sequestration, the capacity of land ecosystems to slow the rise in atmospheric CO 2 concentrations may be smaller than previously assumed. © 2017 John Wiley & Sons Ltd.

  19. Synergy of rising nitrogen depositions and atmospheric CO2 on land carbon uptake moderately offsets global warming

    NASA Astrophysics Data System (ADS)

    Churkina, Galina; Brovkin, Victor; von Bloh, Werner; Trusilova, Kristina; Jung, Martin; Dentener, Frank

    2009-12-01

    Increased carbon uptake of land in response to elevated atmospheric CO2 concentration and nitrogen deposition could slow down the rate of CO2 increase and facilitate climate change mitigation. Using a coupled model of climate, ocean, and land biogeochemistry, we show that atmospheric nitrogen deposition and atmospheric CO2 have a strong synergistic effect on the carbon uptake of land. Our best estimate of the global land carbon uptake in the 1990s is 1.34 PgC/yr. The synergistic effect could explain 47% of this carbon uptake, which is higher than either the effect of increasing nitrogen deposition (29%) or CO2 fertilization (24%). By 2030, rising carbon uptake on land has a potential to reduce atmospheric CO2 concentration by about 41 ppm out of which 16 ppm reduction would come from the synergetic response of land to the CO2 and nitrogen fertilization effects. The strength of the synergy depends largely on the cooccurrence of high nitrogen deposition regions with nonagricultural ecosystems. Our study suggests that reforestation and sensible ecosystem management in industrialized regions may have larger potential for climate change mitigation than anticipated.

  20. On the development of a methodology for extensive in-situ and continuous atmospheric CO2 monitoring

    NASA Astrophysics Data System (ADS)

    Wang, K.; Chang, S.; Jhang, T.

    2010-12-01

    Carbon dioxide is recognized as the dominating greenhouse gas contributing to anthropogenic global warming. Stringent controls on carbon dioxide emissions are viewed as necessary steps in controlling atmospheric carbon dioxide concentrations. From the view point of policy making, regulation of carbon dioxide emissions and its monitoring are keys to the success of stringent controls on carbon dioxide emissions. Especially, extensive atmospheric CO2 monitoring is a crucial step to ensure that CO2 emission control strategies are closely followed. In this work we develop a methodology that enables reliable and accurate in-situ and continuous atmospheric CO2 monitoring for policy making. The methodology comprises the use of gas filter correlation (GFC) instrument for in-situ CO2 monitoring, the use of CO2 working standards accompanying the continuous measurements, and the use of NOAA WMO CO2 standard gases for calibrating the working standards. The use of GFC instruments enables 1-second data sampling frequency with the interference of water vapor removed from added dryer. The CO2 measurements are conducted in the following timed and cycled manner: zero CO2 measurement, two standard CO2 gases measurements, and ambient air measurements. The standard CO2 gases are calibrated again NOAA WMO CO2 standards. The methodology is used in indoor CO2 measurements in a commercial office (about 120 people working inside), ambient CO2 measurements, and installed in a fleet of in-service commercial cargo ships for monitoring CO2 over global marine boundary layer. These measurements demonstrate our method is reliable, accurate, and traceable to NOAA WMO CO2 standards. The portability of the instrument and the working standards make the method readily applied for large-scale and extensive CO2 measurements.

  1. C/O Ratio as a Dimension for Characterizing Exoplanetary Atmospheres

    NASA Astrophysics Data System (ADS)

    Madhusudhan, Nikku

    2012-10-01

    Until recently, infrared observations of exoplanetary atmospheres have typically been interpreted using models that assumed solar elemental abundances. With the chemical composition fixed, attempts have been made to classify hot Jupiter atmospheres on the basis of stellar irradiation. However, recent observations have revealed deviations from predictions based on such classification schemes, and chemical compositions retrieved from some data sets have also indicated non-solar abundances. The data require a two-dimensional (2D) characterization scheme with dependence on both irradiation and chemistry. In this work, we suggest the carbon-to-oxygen (C/O) ratio as an important second dimension for characterizing exoplanetary atmospheres. In hot-hydrogen-dominated atmospheres, the C/O ratio critically influences the relative concentrations of several spectroscopically dominant species. Between a C/O of 0.5 (solar value) and 2, the H2O and CH4 abundances can vary by several orders of magnitude in the observable atmosphere, and new hydrocarbon species such as HCN and C2H2 become prominent for C/O >= 1, while the CO abundance remains almost unchanged. Furthermore, a C/O >= 1 can preclude a strong thermal inversion due to TiO and VO in a hot Jupiter atmosphere, since TiO and VO are naturally underabundant for C/O >= 1. We, therefore, suggest a new 2D classification scheme for hydrogen-dominated exoplanetary atmospheres with irradiation (or temperature) and C/O ratio as the two dimensions. We define four classes in this 2D space (O1, O2, C1, and C2) with distinct chemical, thermal, and spectral properties. Based on the most recent observations, we characterize the thermal structure and C/O ratios of six hot Jupiters (XO-1b, CoRoT-2b, WASP-14b, WASP-19b, WASP-33b, and WASP-12b) in the framework of our proposed 2D classification scheme. While the data for several systems in our sample are consistent with C-rich atmospheres, new observations are required to conclusively

  2. Hemiparasite abundance in an alpine treeline ecotone increases in response to atmospheric CO(2) enrichment.

    PubMed

    Hättenschwiler, Stephan; Zumbrunn, Thomas

    2006-02-01

    Populations of the annual hemiparasites Melampyrum pratense L. and Melampyrum sylvaticum L. were studied at the treeline in the Swiss Alps after 3 years of in situ CO(2) enrichment. The total density of Melampyrum doubled to an average of 44 individuals per square meter at elevated CO(2) compared to ambient CO(2). In response to elevated CO(2), the height of the more abundant and more evenly distributed M. pratense increased by 20%, the number of seeds per fruit by 21%, and the total seed dry mass per fruit by 27%, but the individual seed size did not change. These results suggest that rising atmospheric CO(2) may stimulate the reproductive output and increase the abundance of Melampyrum in the alpine treeline ecotone. Because hemiparasites can have important effects on community dynamics and ecosystem processes, notably the N cycle, changing Melampyrum abundance may potentially influence the functioning of alpine ecosystems in a future CO(2)-rich atmosphere.

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

    NASA Technical Reports Server (NTRS)

    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.

  4. CO oxidation and O2 removal on meteoric material in Venus' atmosphere

    NASA Astrophysics Data System (ADS)

    Frankland, Victoria L.; James, Alexander D.; Carrillo-Sánchez, Juan Diego; Nesvorný, David; Pokorný, Petr; Plane, John M. C.

    2017-11-01

    The heterogeneous oxidation of CO by O2 on olivine, Fe sulfate and Fe oxide particles was studied using a flow tube apparatus between 300 and 680 K. These particles were chosen as possible analogues of unablated cosmic dust and meteoric smoke in Venus' atmosphere. On olivine and Fe oxides, the rate of CO oxidation to CO2 only becomes significant above 450 K. For iron sulfates, CO2 production was not observed until these dust analogues had decomposed into iron oxides at ∼ 540 K. The CO oxidation rate increases significantly with a higher Fe content in the dust, implying that oxidation occurs through Fe active sites (no reaction was observed on Mg2SiO4). The oxidation kinetics can be explained by CO reacting with chemi-sorbed O2 through an Eley-Rideal mechanism, which is supported by electronic structure calculations. Uptake coefficients were measured from 450 to 680 K, yielding: log10(γ (CO on MgFeSiO4)) = (2.9 ± 0.1) × 10-3 T(K) - (8.2 ± 0.1); log10(γ (CO on Fe2SiO4)) = (2.3 ± 0.3) × 10-3 T(K) - (7.7 ± 0.2); log10(γ (CO on FeOOH/Fe2O3)) = (5.6 ± 0.8) × 10-3T(K) - (9.3 ± 0.4). A 1-D atmospheric model of Venus was then constructed to explore the role of heterogeneous oxidation. The cosmic dust input to Venus, mostly originating from Jupiter Family Comets, is around 32 tonnes per Earth day. A chemical ablation model was used to show that ∼34% of this incoming mass ablates, forming meteoric smoke particles which, together with unablated dust particles, provide a significant surface for the heterogeneous oxidation of CO to CO2 in Venus' troposphere. This process should cause almost complete removal of O2 below 40 km, but have a relatively small impact on the CO mixing ratio (since CO is in large excess over O2). Theoretical quantum calculations indicate that the gas-phase oxidation of CO by SO2 in the lower troposphere is not competitive with the heterogeneous oxidation of CO. Finally, the substantial number density of meteoric smoke particles predicted

  5. Spatial variations in atmospheric CO2 concentrations during the ARCTAS-CARB 2008 Summer Campaign

    NASA Astrophysics Data System (ADS)

    Vadrevu, K. P.; Choi, Y.; Vay, S. A.

    2009-12-01

    The Arctic Research of the Composition of the Troposphere from Aircraft and Satellites (ARCTAS) was a major NASA field campaign designed to understand the transport and transformation of trace gases and aerosols on transcontinental and intercontinental scales and their impact on the composition of the arctic atmosphere and climate. Preceding the summer ARCTAS deployment, measurements were conducted over the state of California in collaboration with the California Air Resources Board (CARB) utilizing the airborne chemistry payload already integrated on the NASA DC-8. In situ CO2 measurements were made using a modified infrared CO2 gas analyzer having a precision of 0.1 ppmv and accuracy of ±0.25 ppmv traceable to the WMO scale. This analysis focuses on the atmospheric CO2 variability and biospheric/atmospheric exchange over California. We used multi-satellite remote sensing datasets to relate airborne observations of CO2 to infer sources and sinks. Georeferencing the airborne CO2 transect data with the LANDSAT derived land cover datasets over California suggested significant spatial variations. The airborne CO2 concentrations were found to be 375-380ppm over the Pacific ocean, 385-391ppm in the highly vegetated agricultural areas, 400-420 in the near coastal areas and greater than 425ppmv in the urban areas. Analysis from MODIS fire products suggested significant fires in northern California. CO2 emissions exceeded 425ppmv in the fire affected regions, where mostly Douglas and White Fir conifers and mixed Chaparral vegetation was burnt. Analysis from GOES-East and GOES-West visible satellite imagery suggested significant smoke plumes moving from northern California towards Nevada and Idaho. To infer the biospheric uptake of CO2, we tested the potential correlations between airborne CO2 data and MODIS normalized difference vegetation index (NDVI) and enhanced vegetation index (EVI). Results suggested significant anti-correlations between the airborne CO2 data and

  6. Separating the influence of temperature, drought, and fire on interannual variability in atmospheric CO2

    PubMed Central

    Keppel-Aleks, Gretchen; Wolf, Aaron S; Mu, Mingquan; Doney, Scott C; Morton, Douglas C; Kasibhatla, Prasad S; Miller, John B; Dlugokencky, Edward J; Randerson, James T

    2014-01-01

    The response of the carbon cycle in prognostic Earth system models (ESMs) contributes significant uncertainty to projections of global climate change. Quantifying contributions of known drivers of interannual variability in the growth rate of atmospheric carbon dioxide (CO2) is important for improving the representation of terrestrial ecosystem processes in these ESMs. Several recent studies have identified the temperature dependence of tropical net ecosystem exchange (NEE) as a primary driver of this variability by analyzing a single, globally averaged time series of CO2 anomalies. Here we examined how the temporal evolution of CO2 in different latitude bands may be used to separate contributions from temperature stress, drought stress, and fire emissions to CO2 variability. We developed atmospheric CO2 patterns from each of these mechanisms during 1997–2011 using an atmospheric transport model. NEE responses to temperature, NEE responses to drought, and fire emissions all contributed significantly to CO2 variability in each latitude band, suggesting that no single mechanism was the dominant driver. We found that the sum of drought and fire contributions to CO2 variability exceeded direct NEE responses to temperature in both the Northern and Southern Hemispheres. Additional sensitivity tests revealed that these contributions are masked by temporal and spatial smoothing of CO2 observations. Accounting for fires, the sensitivity of tropical NEE to temperature stress decreased by 25% to 2.9 ± 0.4 Pg C yr−1 K−1. These results underscore the need for accurate attribution of the drivers of CO2 variability prior to using contemporary observations to constrain long-term ESM responses. PMID:26074665

  7. Separating the influence of temperature, drought, and fire on interannual variability in atmospheric CO2.

    PubMed

    Keppel-Aleks, Gretchen; Wolf, Aaron S; Mu, Mingquan; Doney, Scott C; Morton, Douglas C; Kasibhatla, Prasad S; Miller, John B; Dlugokencky, Edward J; Randerson, James T

    2014-11-01

    The response of the carbon cycle in prognostic Earth system models (ESMs) contributes significant uncertainty to projections of global climate change. Quantifying contributions of known drivers of interannual variability in the growth rate of atmospheric carbon dioxide (CO 2 ) is important for improving the representation of terrestrial ecosystem processes in these ESMs. Several recent studies have identified the temperature dependence of tropical net ecosystem exchange (NEE) as a primary driver of this variability by analyzing a single, globally averaged time series of CO 2 anomalies. Here we examined how the temporal evolution of CO 2 in different latitude bands may be used to separate contributions from temperature stress, drought stress, and fire emissions to CO 2 variability. We developed atmospheric CO 2 patterns from each of these mechanisms during 1997-2011 using an atmospheric transport model. NEE responses to temperature, NEE responses to drought, and fire emissions all contributed significantly to CO 2 variability in each latitude band, suggesting that no single mechanism was the dominant driver. We found that the sum of drought and fire contributions to CO 2 variability exceeded direct NEE responses to temperature in both the Northern and Southern Hemispheres. Additional sensitivity tests revealed that these contributions are masked by temporal and spatial smoothing of CO 2 observations. Accounting for fires, the sensitivity of tropical NEE to temperature stress decreased by 25% to 2.9 ± 0.4 Pg C yr -1  K -1 . These results underscore the need for accurate attribution of the drivers of CO 2 variability prior to using contemporary observations to constrain long-term ESM responses.

  8. Relationship between synoptic scale weather systems and column averaged atmospheric CO2

    NASA Astrophysics Data System (ADS)

    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

  9. Atmospheric CO2 Over the Last 1000 Years: WAIS Divide Ice Core Record

    NASA Astrophysics Data System (ADS)

    Ahn, J.; Brook, E. J.

    2009-04-01

    How atmospheric CO2 varied over the last thousands years is of great interest because we may see not only natural, but also anthropogenic variations (Ruddiman, Climatic Change, 2003). The Law Dome ice cores reveal decadal to centennial variations in CO2 over the last 2000 years (MacFarling Meure et al., Geophys. Res. Lett., 2006). However, these variations have not yet been well confirmed in other ice core records. Here we use a newly drilled WAIS Divide ice core, which is ideal for this purpose because WAIS Divide has relatively high snow accumulation rate and small gas age distribution that allow us to observe decadal CO2 variations with minimal damping. We have started an extensive study of CO2 in WAIS Divide core. So far we have obtained data for 960-1940 A.D. from the WDC05-A core drilled in 2005-2006. 344 ice samples from 103 depths were analyzed and the standard error of the mean is ~0.8 ppm on average. Ancient air in 8~12 g of bubbly ice is liberated by crushing with steel pins at -35 °C and trapped in stainless steel tubes at -262 °C. CO2 mixing ratio in the extracted air is precisely determined using a gas chromatographic method. Details of the high-precision methods are described in Ahn et al. (J. of Glaciology, in press). Our new results show preindustrial atmospheric CO2 variability of ~ 10 ppm. The most striking feature of the record is a rapid atmospheric CO2 decrease of 7~8 ppm within ~20 years at ~ 1600 A.D. Considering the larger smoothing of gas records in the WAIS Divide relative to Law Dome, our results confirm the atmospheric CO2 decrease of ~10 ppm in Law Dome records observed at this time. However, this event is not significant in the Dronning Maud Land ice core (Siegenthaler et al., Tellus, 2005), probably due to more extensive smoothing of gas records in the core. Similar rapid changes of CO2 at other times in the WAIS Divide record need to be confirmed with higher resolution studies. We also found that our WAIS Divide CO2 data are

  10. A Test of Sensitivity to Convective Transport in a Global Atmospheric CO2 Simulation

    NASA Technical Reports Server (NTRS)

    Bian, H.; Kawa, S. R.; Chin, M.; Pawson, S.; Zhu, Z.; Rasch, P.; Wu, S.

    2006-01-01

    Two approximations to convective transport have been implemented in an offline chemistry transport model (CTM) to explore the impact on calculated atmospheric CO2 distributions. GlobalCO2 in the year 2000 is simulated using theCTM driven by assimilated meteorological fields from the NASA s Goddard Earth Observation System Data Assimilation System, Version 4 (GEOS-4). The model simulates atmospheric CO2 by adopting the same CO2 emission inventory and dynamical modules as described in Kawa et al. (convective transport scheme denoted as Conv1). Conv1 approximates the convective transport by using the bulk convective mass fluxes to redistribute trace gases. The alternate approximation, Conv2, partitions fluxes into updraft and downdraft, as well as into entrainment and detrainment, and has potential to yield a more realistic simulation of vertical redistribution through deep convection. Replacing Conv1 by Conv2 results in an overestimate of CO2 over biospheric sink regions. The largest discrepancies result in a CO2 difference of about 7.8 ppm in the July NH boreal forest, which is about 30% of the CO2 seasonality for that area. These differences are compared to those produced by emission scenario variations constrained by the framework of Intergovernmental Panel on Climate Change (IPCC) to account for possible land use change and residual terrestrial CO2 sink. It is shown that the overestimated CO2 driven by Conv2 can be offset by introducing these supplemental emissions.

  11. Impacts of elevated atmospheric CO2 on nutrient content of important food crops

    NASA Astrophysics Data System (ADS)

    Dietterich, Lee H.; Zanobetti, Antonella; Kloog, Itai; Huybers, Peter; Leakey, Andrew D. B.; Bloom, Arnold J.; Carlisle, Eli; Fernando, Nimesha; Fitzgerald, Glenn; Hasegawa, Toshihiro; Holbrook, N. Michele; Nelson, Randall L.; Norton, Robert; Ottman, Michael J.; Raboy, Victor; Sakai, Hidemitsu; Sartor, Karla A.; Schwartz, Joel; Seneweera, Saman; Usui, Yasuhiro; Yoshinaga, Satoshi; Myers, Samuel S.

    2015-07-01

    One of the many ways that climate change may affect human health is by altering the nutrient content of food crops. However, previous attempts to study the effects of increased atmospheric CO2 on crop nutrition have been limited by small sample sizes and/or artificial growing conditions. Here we present data from a meta-analysis of the nutritional contents of the edible portions of 41 cultivars of six major crop species grown using free-air CO2 enrichment (FACE) technology to expose crops to ambient and elevated CO2 concentrations in otherwise normal field cultivation conditions. This data, collected across three continents, represents over ten times more data on the nutrient content of crops grown in FACE experiments than was previously available. We expect it to be deeply useful to future studies, such as efforts to understand the impacts of elevated atmospheric CO2 on crop macro- and micronutrient concentrations, or attempts to alleviate harmful effects of these changes for the billions of people who depend on these crops for essential nutrients.

  12. Impacts of elevated atmospheric CO2 on nutrient content of important food crops

    PubMed Central

    Dietterich, Lee H.; Zanobetti, Antonella; Kloog, Itai; Huybers, Peter; Leakey, Andrew D. B.; Bloom, Arnold J.; Carlisle, Eli; Fernando, Nimesha; Fitzgerald, Glenn; Hasegawa, Toshihiro; Holbrook, N. Michele; Nelson, Randall L.; Norton, Robert; Ottman, Michael J.; Raboy, Victor; Sakai, Hidemitsu; Sartor, Karla A.; Schwartz, Joel; Seneweera, Saman; Usui, Yasuhiro; Yoshinaga, Satoshi; Myers, Samuel S.

    2015-01-01

    One of the many ways that climate change may affect human health is by altering the nutrient content of food crops. However, previous attempts to study the effects of increased atmospheric CO2 on crop nutrition have been limited by small sample sizes and/or artificial growing conditions. Here we present data from a meta-analysis of the nutritional contents of the edible portions of 41 cultivars of six major crop species grown using free-air CO2 enrichment (FACE) technology to expose crops to ambient and elevated CO2 concentrations in otherwise normal field cultivation conditions. This data, collected across three continents, represents over ten times more data on the nutrient content of crops grown in FACE experiments than was previously available. We expect it to be deeply useful to future studies, such as efforts to understand the impacts of elevated atmospheric CO2 on crop macro- and micronutrient concentrations, or attempts to alleviate harmful effects of these changes for the billions of people who depend on these crops for essential nutrients. PMID:26217490

  13. Intensity-Modulated Continuous-Wave Laser Absorption Spectrometer at 1.57 Micrometer for Atmospheric CO2 Measurements

    NASA Technical Reports Server (NTRS)

    Lin, Bing

    2014-01-01

    Understanding the earth's carbon cycle is essential for diagnosing current and predicting future climates, which requires precise global measurements of atmospheric CO2 through space missions. The Active Sensing of CO2 Emissions over Nights, Days, and Seasons (ASCENDS) space mission will provide accurate global atmospheric CO2 measurements to meet carbon science requirements. The joint team of NASA Langley Research Center and ITT Exelis, Inc. proposes to use the intensity-modulated, continuous-wave (IM-CW) laser absorption spectrometer (LAS) approach for the ASCENDS mission. Prototype LAS instruments have been developed and used to demonstrate the power, signal-to-noise ratio, precision and accuracy, spectral purity, and stability of the measurement and the instrument needed for atmospheric CO2 observations from space. The ranging capability from laser platform to ground surfaces or intermediate backscatter layers is achieved by transmitted range-encoded IM laser signals. Based on the prototype instruments and current lidar technologies, space LAS systems and their CO2 column measurements are analyzed. These studies exhibit a great potential of using IM-CW LAS system for the active space CO2 mission ASCENDS.

  14. Potential effects of elevated atmospheric carbon dioxide (CO2) on coastal wetlands

    USGS Publications Warehouse

    McKee, Karen

    2006-01-01

    Carbon dioxide (CO2) concentration in the atmosphere has steadily increased from 280 parts per million (ppm) in preindustrial times to 381 ppm today and is predicted by some models to double within the next century. Some of the important pathways whereby changes in atmospheric CO2 may impact coastal wetlands include changes in temperature, rainfall, and hurricane intensity (fig. 1). Increases in CO2 can contribute to global warming, which may (1) accelerate sea-level rise through melting of polar ice fields and steric expansion of oceans, (2) alter rainfall patterns and salinity regimes, and (3) change the intensity and frequency of tropical storms and hurricanes. Sea-level rise combined with changes in storm activity may affect erosion and sedimentation rates and patterns in coastal wetlands and maintenance of soil elevations.Feedback loops between plant growth and hydroedaphic conditions also contribute to maintenance of marsh elevations through accumulation of organic matter. Although increasing CO2 concentration may contribute to global warming and climate changes, it may also have a direct impact on plant growth and development by stimulating photosynthesis or improving water use efficiency. Scientists with the U.S. Geological Survey are examining responses of wetland plants to elevated CO2 concentration and other factors. This research will lead to a better understanding of future changes in marsh species composition, successional rates and patterns, ecological functioning, and vulnerability to sea-level rise and other global change factors.

  15. Biomass and toxicity responses of poison ivy (Toxicodendron radicans) to elevated atmospheric CO2.

    PubMed

    Mohan, Jacqueline E; Ziska, Lewis H; Schlesinger, William H; Thomas, Richard B; Sicher, Richard C; George, Kate; Clark, James S

    2006-06-13

    Contact with poison ivy (Toxicodendron radicans) is one of the most widely reported ailments at poison centers in the United States, and this plant has been introduced throughout the world, where it occurs with other allergenic members of the cashew family (Anacardiaceae). Approximately 80% of humans develop dermatitis upon exposure to the carbon-based active compound, urushiol. It is not known how poison ivy might respond to increasing concentrations of atmospheric carbon dioxide (CO(2)), but previous work done in controlled growth chambers shows that other vines exhibit large growth enhancement from elevated CO(2). Rising CO(2) is potentially responsible for the increased vine abundance that is inhibiting forest regeneration and increasing tree mortality around the world. In this 6-year study at the Duke University Free-Air CO(2) Enrichment experiment, we show that elevated atmospheric CO(2) in an intact forest ecosystem increases photosynthesis, water use efficiency, growth, and population biomass of poison ivy. The CO(2) growth stimulation exceeds that of most other woody species. Furthermore, high-CO(2) plants produce a more allergenic form of urushiol. Our results indicate that Toxicodendron taxa will become more abundant and more "toxic" in the future, potentially affecting global forest dynamics and human health.

  16. Biomass and toxicity responses of poison ivy (Toxicodendron radicans) to elevated atmospheric CO2

    PubMed Central

    Mohan, Jacqueline E.; Ziska, Lewis H.; Schlesinger, William H.; Thomas, Richard B.; Sicher, Richard C.; George, Kate; Clark, James S.

    2006-01-01

    Contact with poison ivy (Toxicodendron radicans) is one of the most widely reported ailments at poison centers in the United States, and this plant has been introduced throughout the world, where it occurs with other allergenic members of the cashew family (Anacardiaceae). Approximately 80% of humans develop dermatitis upon exposure to the carbon-based active compound, urushiol. It is not known how poison ivy might respond to increasing concentrations of atmospheric carbon dioxide (CO2), but previous work done in controlled growth chambers shows that other vines exhibit large growth enhancement from elevated CO2. Rising CO2 is potentially responsible for the increased vine abundance that is inhibiting forest regeneration and increasing tree mortality around the world. In this 6-year study at the Duke University Free-Air CO2 Enrichment experiment, we show that elevated atmospheric CO2 in an intact forest ecosystem increases photosynthesis, water use efficiency, growth, and population biomass of poison ivy. The CO2 growth stimulation exceeds that of most other woody species. Furthermore, high-CO2 plants produce a more allergenic form of urushiol. Our results indicate that Toxicodendron taxa will become more abundant and more “toxic” in the future, potentially affecting global forest dynamics and human health. PMID:16754866

  17. The Martian climate: Energy balance models with CO2/H2O atmospheres

    NASA Technical Reports Server (NTRS)

    Hoffert, M. I.

    1984-01-01

    Progress in the development of a multi-reservoir, time dependent energy balance climate model for Mars driven by prescribed insolation at the top of the atmosphere is reported. The first approximately half-year of the program was devoted to assembling and testing components of the full model. Specific accomplishments were made on a longwave radiation code, coupling seasonal solar input to a ground temperature simulation, and conceptualizing an approach to modeling the seasonal pressure waves that develop in the Martian atmosphere as a result of sublimation and condensation of CO2 in polar regions.

  18. Comparing Global Atmospheric CO2 Flux and Transport Models with Remote Sensing (and Other) Observations

    NASA Technical Reports Server (NTRS)

    Kawa, S. R.; Collatz, G. J.; Pawson, S.; Wennberg, P. O.; Wofsy, S. C.; Andrews, A. E.

    2010-01-01

    We report recent progress derived from comparison of global CO2 flux and transport models with new remote sensing and other sources of CO2 data including those from satellite. The overall objective of this activity is to improve the process models that represent our understanding of the workings of the atmospheric carbon cycle. Model estimates of CO2 surface flux and atmospheric transport processes are required for initial constraints on inverse analyses, to connect atmospheric observations to the location of surface sources and sinks, to provide the basic framework for carbon data assimilation, and ultimately for future projections of carbon-climate interactions. Models can also be used to test consistency within and between CO2 data sets under varying geophysical states. Here we focus on simulated CO2 fluxes from terrestrial vegetation and atmospheric transport mutually constrained by analyzed meteorological fields from the Goddard Modeling and Assimilation Office for the period 2000 through 2009. Use of assimilated meteorological data enables direct model comparison to observations across a wide range of scales of variability. The biospheric fluxes are produced by the CASA model at 1x1 degrees on a monthly mean basis, modulated hourly with analyzed temperature and sunlight. Both physiological and biomass burning fluxes are derived using satellite observations of vegetation, burned area (as in GFED-3), and analyzed meteorology. For the purposes of comparison to CO2 data, fossil fuel and ocean fluxes are also included in the transport simulations. In this presentation we evaluate the model's ability to simulate CO2 flux and mixing ratio variability in comparison to remote sensing observations from TCCON, GOSAT, and AIRS as well as relevant in situ observations. Examples of the influence of key process representations are shown from both forward and inverse model comparisons. We find that the model can resolve much of the synoptic, seasonal, and interannual

  19. The Increasing Concentrations of Atmospheric CO2: How Much, When and Why?

    DOE Data Explorer

    Marland, Gregg [Environmental Sciences Division, Oak Ridge National Laboratory (ORNL); Boden, Tom [Environmental Sciences Division, Oak Ridge National Laboratory (ORNL)

    2009-01-01

    There is now a sense that the world community has achieved a broad consensus that: 1.) the atmospheric concentration of carbon dioxide (CO2) is increasing, 2.) this increase is due largely to the combustion of fossil fuels, and 3.) this increase is likely to lead to changes in the global climate. This consensus is sufficiently strong that virtually all countries are involved in trying to achieve a functioning agreement on how to confront, and mitigate, these changes in climate. This paper reviews the first two of these components in a quantitative way. We look at the data on the atmospheric concentration of carbon dioxide and on the magnitude of fossil-fuel combustion, and we examine the trends in both. We review the extent to which cause and effect can be demonstrated between the trends in fossil-fuel burning and the trends in atmospheric CO2 concentration. Finally, we look at scenarios for the future use of fossil fuels and what these portend for the future of atmospheric chemistry. Along the way we examine how and where fossil fuels are used on the Earth and some of the issues that are raised by any effort to reduce fossil-fuel use.

  20. Effects of atmospheric CO[sub 2] and soil NO[sub 3][sup [minus

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Lindroth, R.L.; Kinney, K.K.

    1993-06-01

    Physiological and growth responses of trees to elevated atmospheric CO[sub 2] are influenced by soil nutrient availability. Interactive effects of these factors on tree chemical composition, however, are largely unknown. We used a split-plot experimental design to assess the impact of CO[sub 2] (whole plots; 355 and 650 ppm) and soil NO[sub 3][sup [minus

  1. Shifting carbon flow from roots into associated microbial communities in response to elevated atmospheric CO2.

    PubMed

    Drigo, Barbara; Pijl, Agata S; Duyts, Henk; Kielak, Anna M; Gamper, Hannes A; Houtekamer, Marco J; Boschker, Henricus T S; Bodelier, Paul L E; Whiteley, Andrew S; van Veen, Johannes A; Kowalchuk, George A

    2010-06-15

    Rising atmospheric CO(2) levels are predicted to have major consequences on carbon cycling and the functioning of terrestrial ecosystems. Increased photosynthetic activity is expected, especially for C-3 plants, thereby influencing vegetation dynamics; however, little is known about the path of fixed carbon into soil-borne communities and resulting feedbacks on ecosystem function. Here, we examine how arbuscular mycorrhizal fungi (AMF) act as a major conduit in the transfer of carbon between plants and soil and how elevated atmospheric CO(2) modulates the belowground translocation pathway of plant-fixed carbon. Shifts in active AMF species under elevated atmospheric CO(2) conditions are coupled to changes within active rhizosphere bacterial and fungal communities. Thus, as opposed to simply increasing the activity of soil-borne microbes through enhanced rhizodeposition, elevated atmospheric CO(2) clearly evokes the emergence of distinct opportunistic plant-associated microbial communities. Analyses involving RNA-based stable isotope probing, neutral/phosphate lipid fatty acids stable isotope probing, community fingerprinting, and real-time PCR allowed us to trace plant-fixed carbon to the affected soil-borne microorganisms. Based on our data, we present a conceptual model in which plant-assimilated carbon is rapidly transferred to AMF, followed by a slower release from AMF to the bacterial and fungal populations well-adapted to the prevailing (myco-)rhizosphere conditions. This model provides a general framework for reappraising carbon-flow paths in soils, facilitating predictions of future interactions between rising atmospheric CO(2) concentrations and terrestrial ecosystems.

  2. Global carbon - nitrogen - phosphorus cycle interactions: A key to solving the atmospheric CO2 balance problem?

    NASA Technical Reports Server (NTRS)

    Peterson, B. J.; Mellillo, J. M.

    1984-01-01

    If all biotic sinks of atmospheric CO2 reported were added a value of about 0.4 Gt C/yr would be found. For each category, a very high (non-conservative) estimate was used. This still does not provide a sufficient basis for achieving a balance between the sources and sinks of atmospheric CO2. The bulk of the discrepancy lies in a combination of errors in the major terms, the greatest being in a combination of errors in the major terms, the greatest being in the net biotic release and ocean uptake segments, but smaller errors or biases may exist in calculations of the rate of atmospheric CO2 increase and total fossil fuel use as well. The reason why biotic sinks are not capable of balancing the CO2 increase via nutrient-matching in the short-term is apparent from a comparison of the stoichiometry of the sources and sinks. The burning of fossil fuels and forest biomass releases much more CO2-carbon than is sequestered as organic carbon.

  3. Atmospheric pCO2 Reconstructed across the Early Eocene Hyperthermals

    NASA Astrophysics Data System (ADS)

    Cui, Y.; Schubert, B.

    2015-12-01

    Negative carbon isotope excursions (CIEs) are commonly associated with extreme global warming. The Early Eocene is punctuated by five such CIEs, the Paleocene-Eocene thermal maximum (PETM, ca. 55.8 Ma), H1 (ca. 53.6 Ma), H2 (ca. 53.5 Ma), I1 (ca. 53.3 Ma), and I2 (ca. 53.2 Ma), each characterized by global warming. The negative CIEs are recognized in both marine and terrestrial substrates, but the terrestrial substrates exhibit a larger absolute magnitude CIE than the marine substrates. Here we reconcile the difference in CIE magnitude between the terrestrial and marine substrates for each of these events by accounting for the additional carbon isotope fractionation by C3 land plants in response to increased atmospheric pCO2. Our analysis yields background and peak pCO2 values for each of the events. Assuming a common mechanism for each event, we calculate that background pCO2 was not static across the Early Eocene, with the highest background pCO2 immediately prior to I2, the last of the five CIEs. Background pCO2 is dependent on the source used in our analysis with values ranging from 300 to 720 ppmv provided an injection of 13C-depleted carbon with δ13C value of -60‰ (e.g. biogenic methane). The peak pCO2 during each event scales according to the magnitude of CIE, and is therefore greatest during the PETM and smallest during H2. Both background and peak pCO2 are higher if we assume a mechanism of permafrost thawing (δ13C = -25‰). Our reconstruction of pCO2 across these events is consistent with trends in the δ18O value of deep-sea benthic foraminifera, suggesting a strong link between pCO2 and temperature during the Early Eocene.

  4. Recharge of the early atmosphere of Mars by impact-induced release of CO2

    NASA Technical Reports Server (NTRS)

    Carr, Michael H.

    1989-01-01

    The question as to whether high impact rates early in the history of Mars could have aided in maintaining a relatively thick CO2 atmosphere is discussed. Such impacts could have released CO2 into the atmosphere by burial, by shock-induced release during impact events, and by the addition of carbon to Mars from the impacting bolides. On the assumption that cratering rates on Mars were comparable to those of the moon's Nectarial period, burial rates are a result of 'impact gardening' at the end of heavy bombardment are estimated to have ranged from 20 to 45 m/million years; at these rates, 0.1-0.2 bar of CO2 would have been released every 10 million years as a result of burial to depths at which carbonate dissociation temperatures are encountered.

  5. Glyphosate Resistance of C3 and C4 Weeds under Rising Atmospheric CO2

    PubMed Central

    Fernando, Nimesha; Manalil, Sudheesh; Florentine, Singarayer K.; Chauhan, Bhagirath S.; Seneweera, Saman

    2016-01-01

    The present paper reviews current knowledge on how changes of plant metabolism under elevated CO2 concentrations (e[CO2]) can affect the development of the glyphosate resistance of C3 and C4 weeds. Among the chemical herbicides, glyphosate, which is a non-selective and post-emergence herbicide, is currently the most widely used herbicide in global agriculture. As a consequence, glyphosate resistant weeds, particularly in major field crops, are a widespread problem and are becoming a significant challenge to future global food production. Of particular interest here it is known that the biochemical processes involved in photosynthetic pathways of C3 and C4 plants are different, which may have relevance to their competitive development under changing environmental conditions. It has already been shown that plant anatomical, morphological, and physiological changes under e[CO2] can be different, based on (i) the plant’s functional group, (ii) the available soil nutrients, and (iii) the governing water status. In this respect, C3 species are likely to have a major developmental advantage under a CO2 rich atmosphere, by being able to capitalize on the overall stimulatory effect of e[CO2]. For example, many tropical weed grass species fix CO2 from the atmosphere via the C4 photosynthetic pathway, which is a complex anatomical and biochemical variant of the C3 pathway. Thus, based on our current knowledge of CO2 fixing, it would appear obvious that the development of a glyphosate-resistant mechanism would be easier under an e[CO2] in C3 weeds which have a simpler photosynthetic pathway, than for C4 weeds. However, notwithstanding this logical argument, a better understanding of the biochemical, genetic, and molecular measures by which plants develop glyphosate resistance and how e[CO2] affects these measures will be important before attempting to innovate sustainable technology to manage the glyphosate-resistant evolution of weeds under e[CO2]. Such information will be

  6. Glyphosate Resistance of C3 and C4 Weeds under Rising Atmospheric CO2.

    PubMed

    Fernando, Nimesha; Manalil, Sudheesh; Florentine, Singarayer K; Chauhan, Bhagirath S; Seneweera, Saman

    2016-01-01

    The present paper reviews current knowledge on how changes of plant metabolism under elevated CO2 concentrations (e[CO2]) can affect the development of the glyphosate resistance of C3 and C4 weeds. Among the chemical herbicides, glyphosate, which is a non-selective and post-emergence herbicide, is currently the most widely used herbicide in global agriculture. As a consequence, glyphosate resistant weeds, particularly in major field crops, are a widespread problem and are becoming a significant challenge to future global food production. Of particular interest here it is known that the biochemical processes involved in photosynthetic pathways of C3 and C4 plants are different, which may have relevance to their competitive development under changing environmental conditions. It has already been shown that plant anatomical, morphological, and physiological changes under e[CO2] can be different, based on (i) the plant's functional group, (ii) the available soil nutrients, and (iii) the governing water status. In this respect, C3 species are likely to have a major developmental advantage under a CO2 rich atmosphere, by being able to capitalize on the overall stimulatory effect of e[CO2]. For example, many tropical weed grass species fix CO2 from the atmosphere via the C4 photosynthetic pathway, which is a complex anatomical and biochemical variant of the C3 pathway. Thus, based on our current knowledge of CO2 fixing, it would appear obvious that the development of a glyphosate-resistant mechanism would be easier under an e[CO2] in C3 weeds which have a simpler photosynthetic pathway, than for C4 weeds. However, notwithstanding this logical argument, a better understanding of the biochemical, genetic, and molecular measures by which plants develop glyphosate resistance and how e[CO2] affects these measures will be important before attempting to innovate sustainable technology to manage the glyphosate-resistant evolution of weeds under e[CO2]. Such information will be of

  7. The use of forest stand age information in an atmospheric CO2 inversion applied to North America

    Treesearch

    F. Deng; J.M. Chen; Y. Pan; W. Peters; R. Birdsey; K. McCullough; J. Xiao

    2013-01-01

    Atmospheric inversions have become an important tool in quantifying carbon dioxide (CO2) sinks and sources at a variety of spatiotemporal scales, but associated large uncertainties restrain the inversion research community from reaching agreement on many important subjects. We enhanced an atmospheric inversion of the CO2...

  8. [Characteristics of CO2 flux before and in the heating period at urban complex underlying surface area].

    PubMed

    Jia, Qing-yu; Zhou, Guang-sheng; Wang, Yu; Liu, Xiao-mei

    2010-04-01

    Urban areas were significant contributors to global carbon dioxide emissions. The eddy covariance (EC) was used to measure carbon dioxide (CO2) concentration and flux data at urban area in Shenyang. This research analyzed the characteristics of atmospheric CO2 concentration and flux in October 2008 to November 2008 period before and in the heating period. The results showed that the daily variation of CO2 concentration was two-peak curve. The first peak time appeared as same as sunrise time, while the second peak time impacted by vehicles and heating. The result of CO2 flux showed that urban atmospheric CO2 was net emissions, vegetation photosynthesis absorbed CO2 of traffic, the CO2 flux peak appeared at 17:15-18:15 in the heating period, CO2 emission increased 29.37 g x (m2 x d)(-1) in the heating period than that before the heating period; there was corresponding relationship between CO2 flux and the time when temperature peak and sensible heating flux (Hc) turn positive. The results also indicated that atmospheric CO2 concentration and its flux were affected seriously by both wind direction and carbon sources.

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

    NASA Astrophysics Data System (ADS)

    Peylin, P.; Law, R. M.; Gurney, K. R.; Chevallier, F.; Jacobson, A. R.; Maki, T.; Niwa, Y.; Patra, P. K.; Peters, W.; Rayner, P. J.; Rödenbeck, C.; van der Laan-Luijkx, I. T.; Zhang, X.

    2013-10-01

    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 the northern land (at the

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

    NASA Astrophysics Data System (ADS)

    Peylin, P.; Law, R. M.; Gurney, K. R.; Chevallier, F.; Jacobson, A. R.; Maki, T.; Niwa, Y.; Patra, P. K.; Peters, W.; Rayner, P. J.; Rödenbeck, C.; Zhang, X.

    2013-03-01

    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 2009. 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 (-3.3 Pg Cy-1 (±0.6 standard deviation)) nearly equally spread between land and ocean, a significant although more variable source over the tropics (1.6 ± 1.0 Pg Cy-1) and a compensatory sink of similar magnitude in the south (-1.4 ± 0.6 Pg Cy-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 1.05 versus 0.34 Pg Cy-1 for the 1996-2007 period), with much higher consistency amoung the inversions for the land. While the tropical land explains most of the IAV (stdev ∼ 0.69 Pg Cy-1), the northern and southern land also contribute (stdev ∼ 0.39 Pg Cy-1). Most inversions tend to indicate an increase of the northern land carbon uptake through the 2000s (around 0.11 Pg Cy-1), shared by North America and North Asia. The mean seasonal cycle appears to be well constrained by the atmospheric data over the northern land (at the continental scale), but still highly dependent on

  11. C/O RATIO AS A DIMENSION FOR CHARACTERIZING EXOPLANETARY ATMOSPHERES

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Madhusudhan, Nikku, E-mail: Nikku.Madhusudhan@yale.edu; Department of Astronomy, Yale University, New Haven, CT 06511

    2012-10-10

    Until recently, infrared observations of exoplanetary atmospheres have typically been interpreted using models that assumed solar elemental abundances. With the chemical composition fixed, attempts have been made to classify hot Jupiter atmospheres on the basis of stellar irradiation. However, recent observations have revealed deviations from predictions based on such classification schemes, and chemical compositions retrieved from some data sets have also indicated non-solar abundances. The data require a two-dimensional (2D) characterization scheme with dependence on both irradiation and chemistry. In this work, we suggest the carbon-to-oxygen (C/O) ratio as an important second dimension for characterizing exoplanetary atmospheres. In hot-hydrogen-dominated atmospheres,more » the C/O ratio critically influences the relative concentrations of several spectroscopically dominant species. Between a C/O of 0.5 (solar value) and 2, the H{sub 2}O and CH{sub 4} abundances can vary by several orders of magnitude in the observable atmosphere, and new hydrocarbon species such as HCN and C{sub 2}H{sub 2} become prominent for C/O {>=} 1, while the CO abundance remains almost unchanged. Furthermore, a C/O {>=} 1 can preclude a strong thermal inversion due to TiO and VO in a hot Jupiter atmosphere, since TiO and VO are naturally underabundant for C/O {>=} 1. We, therefore, suggest a new 2D classification scheme for hydrogen-dominated exoplanetary atmospheres with irradiation (or temperature) and C/O ratio as the two dimensions. We define four classes in this 2D space (O1, O2, C1, and C2) with distinct chemical, thermal, and spectral properties. Based on the most recent observations, we characterize the thermal structure and C/O ratios of six hot Jupiters (XO-1b, CoRoT-2b, WASP-14b, WASP-19b, WASP-33b, and WASP-12b) in the framework of our proposed 2D classification scheme. While the data for several systems in our sample are consistent with C-rich atmospheres, new

  12. Organic chemistry in a CO2 rich early Earth atmosphere

    NASA Astrophysics Data System (ADS)

    Fleury, Benjamin; Carrasco, Nathalie; Millan, Maëva; Vettier, Ludovic; Szopa, Cyril

    2017-12-01

    The emergence of life on the Earth has required a prior organic chemistry leading to the formation of prebiotic molecules. The origin and the evolution of the organic matter on the early Earth is not yet firmly understood. Several hypothesis, possibly complementary, are considered. They can be divided in two categories: endogenous and exogenous sources. In this work we investigate the contribution of a specific endogenous source: the organic chemistry occurring in the ionosphere of the early Earth where the significant VUV contribution of the young Sun involved an efficient formation of reactive species. We address the issue whether this chemistry can lead to the formation of complex organic compounds with CO2 as only source of carbon in an early atmosphere made of N2, CO2 and H2, by mimicking experimentally this type of chemistry using a low pressure plasma reactor. By analyzing the gaseous phase composition, we strictly identified the formation of H2O, NH3, N2O and C2N2. The formation of a solid organic phase is also observed, confirming the possibility to trigger organic chemistry in the upper atmosphere of the early Earth. The identification of Nitrogen-bearing chemical functions in the solid highlights the possibility for an efficient ionospheric chemistry to provide prebiotic material on the early Earth.

  13. Combined Effects of Deforestation and Doubled Atmospheric CO2 Concentrations on the Climate of Amazonia.

    NASA Astrophysics Data System (ADS)

    Costa, Marcos Heil; Foley, Jonathan A.

    2000-01-01

    It is generally expected that the Amazon basin will experience at least two major environmental changes during the next few decades and centuries: 1) increasing areas of forest will be converted to pasture and cropland, and 2) concentrations of atmospheric CO2 will continue to rise. In this study, the authors use the National Center for Atmospheric Research GENESIS atmospheric general circulation model, coupled to the Integrated Biosphere Simulator, to determine the combined effects of large-scale deforestation and increased CO2 concentrations (including both physiological and radiative effects) on Amazonian climate.In these simulations, deforestation decreases basin-average precipitation by 0.73 mm day1 over the basin, as a consequence of the general reduction in vertical motion above the deforested area (although there are some small regions with increased vertical motion). The overall effect of doubled CO2 concentrations in Amazonia is an increase in basin-average precipitation of 0.28 mm day1. The combined effect of deforestation and doubled CO2, including the interactions among the processes, is a decrease in the basin-average precipitation of 0.42 mm day1. While the effects of deforestation and increasing CO2 concentrations on precipitation tend to counteract one another, both processes work to warm the Amazon basin. The effect of deforestation and increasing CO2 concentrations both tend to increase surface temperature, mainly because of decreases in evapotranspiration and the radiative effect of CO2. The combined effect of deforestation and doubled CO2, including the interactions among the processes, increases the basin-average temperature by roughly 3.5°C.

  14. Effectiveness of carbon dioxide removal in lowering atmospheric CO2 and reversing global warming in the context of 1.5 degrees

    NASA Astrophysics Data System (ADS)

    Zickfeld, K.; Azevedo, D.

    2017-12-01

    The majority of emissions scenarios that limit warming to 2°C, and nearly all emission scenarios that do not exceed 1.5°C warming by the year 2100 require artificial removal of CO2 from the atmosphere. Carbon dioxide removal (CDR) technologies in these scenarios are required to offset emissions from sectors that are difficult or costly to decarbonize and to generate global `net negative' emissions, allowing to compensate for earlier emissions and to meet long-term climate stabilization targets after overshoot. Only a few studies have explored the Earth system response to CDR and large uncertainties exist regarding the effect of CDR on the carbon cycle and its effectiveness in reversing climate impacts after overshoot. Here we explore the effectiveness of CDR in lowering atmospheric CO2 ("carbon cycle effectiveness") and cool global climate ("cooling effectiveness"). We force the University of Victoria Earth System Climate Model, a model of intermediate complexity, with a set of negative CO2 emissions pulses of different magnitude and applied from different background atmospheric CO2 concentrations. We find the carbon cycle effectiveness of CDR - defined as the change in atmospheric CO2 per unit CO2 removed - decreases with the amount of CO2 removed from the atmosphere and increases at higher background CO2 concentrations from which CDR is applied due to nonlinear responses of carbon sinks to CO2 and climate. The cooling effectiveness - defined as the change in global mean surface air temperature per unit CO2 removed - on the other hand, is largely insensitive to the amount of CO2 removed, but decreases if CDR is applied at higher atmospheric CO2 concentrations, due to the logarithmic relationship between atmospheric CO2 and radiative forcing. Based on our results we conclude that CDR is more effective in restoring a lower atmospheric CO2 concentration and reversing impacts directly linked to CO2 at lower levels of overshoot. CDR's effectiveness in restoring a

  15. Atmospheric CO2 and O3 alter competition for soil nitrogen in developing forests

    Treesearch

    Donald R. Zak; Mark E. Kubiske; Kurt S. Pregitzer; Andrew J. Burton

    2012-01-01

    Plant growth responses to rising atmospheric CO2 and O3 vary among genotypes and between species, which could plausibly influence the strength of competitive interactions for soil N. Ascribable to the size-symmetric nature of belowground competition, we reasoned that differential growth responses to CO2...

  16. Stable Isotope Measurements of Martian Atmospheric CO2 at the Phoenix Landing Site

    NASA Astrophysics Data System (ADS)

    Niles, Paul B.; Boynton, William V.; Hoffman, John H.; Ming, Douglas W.; Hamara, Dave

    2010-09-01

    Carbon dioxide is a primary component of the martian atmosphere and reacts readily with water and silicate rocks. Thus, the stable isotopic composition of CO2 can reveal much about the history of volatiles on the planet. The Mars Phoenix spacecraft measurements of carbon isotopes [referenced to the Vienna Pee Dee belemnite (VPDB)] [δ13CVPDB = -2.5 ± 4.3 per mil (‰)] and oxygen isotopes [referenced to the Vienna standard mean ocean water (VSMOW)] (δ18OVSMOW = 31.0 ± 5.7‰), reported here, indicate that CO2 is heavily influenced by modern volcanic degassing and equilibration with liquid water. When combined with data from the martian meteorites, a general model can be constructed that constrains the history of water, volcanism, atmospheric evolution, and weathering on Mars. This suggests that low-temperature water-rock interaction has been dominant throughout martian history, carbonate formation is active and ongoing, and recent volcanic degassing has played a substantial role in the composition of the modern atmosphere.

  17. The deep atmosphere of Venus and the possible role of density-driven separation of CO2 and N2

    NASA Astrophysics Data System (ADS)

    Lebonnois, Sebastien; Schubert, Gerald

    2017-07-01

    With temperatures around 700 K and pressures of around 75 bar, the deepest 12 km of the atmosphere of Venus are so hot and dense that the atmosphere behaves like a supercritical fluid. The Soviet VeGa-2 probe descended through the atmosphere in 1985 and obtained the only reliable temperature profile for the deep Venusian atmosphere thus far. In this temperature profile, the atmosphere appears to be highly unstable at altitudes below 7 km, contrary to expectations. We argue that the VeGa-2 temperature profile could be explained by a change in the atmospheric gas composition, and thus molecular mass, with depth. We propose that the deep atmosphere consists of a non-homogeneous layer in which the abundance of N2--the second most abundant constituent of the Venusian atmosphere after CO2--gradually decreases to near-zero at the surface. It is difficult to explain a decline in N2 towards the surface with known nitrogen sources and sinks for Venus. Instead we suggest, partly based on experiments on supercritical fluids, that density-driven separation of N2 from CO2 can occur under the high pressures of Venus's deep atmosphere, possibly by molecular diffusion, or by natural density-driven convection. If so, the amount of nitrogen in the atmosphere of Venus is 15% lower than commonly assumed. We suggest that similar density-driven separation could occur in other massive planetary atmospheres.

  18. Does Size Matter? Atmospheric CO2 May Be a Stronger Driver of Stomatal Closing Rate Than Stomatal Size in Taxa That Diversified under Low CO2.

    PubMed

    Elliott-Kingston, Caroline; Haworth, Matthew; Yearsley, Jon M; Batke, Sven P; Lawson, Tracy; McElwain, Jennifer C

    2016-01-01

    One strategy for plants to optimize stomatal function is to open and close their stomata quickly in response to environmental signals. It is generally assumed that small stomata can alter aperture faster than large stomata. We tested the hypothesis that species with small stomata close faster than species with larger stomata in response to darkness by comparing rate of stomatal closure across an evolutionary range of species including ferns, cycads, conifers, and angiosperms under controlled ambient conditions (380 ppm CO2; 20.9% O2). The two species with fastest half-closure time and the two species with slowest half-closure time had large stomata while the remaining three species had small stomata, implying that closing rate was not correlated with stomatal size in these species. Neither was response time correlated with stomatal density, phylogeny, functional group, or life strategy. Our results suggest that past atmospheric CO2 concentration during time of taxa diversification may influence stomatal response time. We show that species which last diversified under low or declining atmospheric CO2 concentration close stomata faster than species that last diversified in a high CO2 world. Low atmospheric [CO2] during taxa diversification may have placed a selection pressure on plants to accelerate stomatal closing to maintain adequate internal CO2 and optimize water use efficiency.

  19. Does Size Matter? Atmospheric CO2 May Be a Stronger Driver of Stomatal Closing Rate Than Stomatal Size in Taxa That Diversified under Low CO2

    PubMed Central

    Elliott-Kingston, Caroline; Haworth, Matthew; Yearsley, Jon M.; Batke, Sven P.; Lawson, Tracy; McElwain, Jennifer C.

    2016-01-01

    One strategy for plants to optimize stomatal function is to open and close their stomata quickly in response to environmental signals. It is generally assumed that small stomata can alter aperture faster than large stomata. We tested the hypothesis that species with small stomata close faster than species with larger stomata in response to darkness by comparing rate of stomatal closure across an evolutionary range of species including ferns, cycads, conifers, and angiosperms under controlled ambient conditions (380 ppm CO2; 20.9% O2). The two species with fastest half-closure time and the two species with slowest half-closure time had large stomata while the remaining three species had small stomata, implying that closing rate was not correlated with stomatal size in these species. Neither was response time correlated with stomatal density, phylogeny, functional group, or life strategy. Our results suggest that past atmospheric CO2 concentration during time of taxa diversification may influence stomatal response time. We show that species which last diversified under low or declining atmospheric CO2 concentration close stomata faster than species that last diversified in a high CO2 world. Low atmospheric [CO2] during taxa diversification may have placed a selection pressure on plants to accelerate stomatal closing to maintain adequate internal CO2 and optimize water use efficiency. PMID:27605929

  20. Biosphere-atmosphere Exchange of CO2 in a Subtropical Mangrove Wetland in Hong Kong

    NASA Astrophysics Data System (ADS)

    Liu, J.; Neogi, S.; Lai, D. Y. F.

    2017-12-01

    Mangrove ecosystems play an important role in the global carbon cycle due to their high primary productivity, carbon-rich sediment, and sensitivity to climate change. Yet, there is currently a paucity of studies that quantify the biosphere-atmosphere exchange of GHGs in mangrove wetlands continuously at the ecosystem level. In this study, the temporal variability of net ecosystem CO2 exchange (NEE) between the Kandelia obovata mangrove and the atmosphere was determined in the Mai Po Marshes Nature Reserve of subtropical Hong Kong using an eddy covariance system between February 2016 and January 2017. The daytime half-hourly NEE ranged between -5.0 and +3.3 µmol m-2 s-1, while the maximum nighttime NEE could reach +5.0 µmol m-2 s-1 during the wet, warm season. Temperature, photosynthetic photon flux density (PPFD), vapor pressure deficit (VPD), and surface water salinity were some key physical and hydrological controls of NEE. Tidal activity could also exert profound influence on CO2 fluxes in this mangrove ecosystem by exporting dissolved carbon to adjacent estuary and inhibiting soil respiration during the inundation period. Overall, this coastal mangrove was a net sink of atmospheric CO2. Our results suggest that the ability of subtropical mangrove ecosystems in sequestering CO2 could be highly dependent on future changes in temperature, precipitation, and salinity.

  1. Lidar remote sensing of laser-induced incandescence on light absorbing particles in the atmosphere.

    PubMed

    Miffre, Alain; Anselmo, Christophe; Geffroy, Sylvain; Fréjafon, Emeric; Rairoux, Patrick

    2015-02-09

    Carbon aerosol is now recognized as a major uncertainty on climate change and public health, and specific instruments are required to address the time and space evolution of this aerosol, which efficiently absorbs light. In this paper, we report an experiment, based on coupling lidar remote sensing with Laser-Induced-Incandescence (LII), which allows, in agreement with Planck's law, to retrieve the vertical profile of very low thermal radiation emitted by light-absorbing particles in an urban atmosphere over several hundred meters altitude. Accordingly, we set the LII-lidar formalism and equation and addressed the main features of LII-lidar in the atmosphere by numerically simulating the LII-lidar signal. We believe atmospheric LII-lidar to be a promising tool for radiative transfer, especially when combined with elastic backscattering lidar, as it may then allow a remote partitioning between strong/less light absorbing carbon aerosols.

  2. Significance of the oceanic CO2 sink for national carbon accounts

    PubMed Central

    McNeil, Ben I

    2006-01-01

    Background Under the United Nations convention on the law of the sea (1982), each participating country maintains exclusive economic and environmental rights within the oceanic region extending 200 nm from its coastline, known as the Exclusive Economic Zone (EEZ). Although the ocean within each EEZ has a vast capacity to absorb anthropogenic CO2 and therefore potentially be used as a carbon sink, it is not mentioned within the Kyoto Protocol most likely due to inadequate quantitative estimates. Here, I use two methods to estimate the anthropogenic CO2 storage and uptake for a typically large EEZ (Australia). Results Depending on whether the Antarctic territory is included I find that during the 1990s between 30–40% of Australia's fossil-fuel CO2 emissions were absorbed by its own EEZ. Conclusion This example highlights the potential significance of the EEZ carbon sink for national carbon accounts. However, this 'natural anthropogenic CO2 sink' could be used as a disincentive for certain nations to reduce their anthropogenic CO2 emissions, which would ultimately dampen global efforts to reduce atmospheric CO2 concentrations. Since the oceanic anthropogenic CO2 sink has limited ability to be controlled by human activities, current and future international climate change policies should have an explicit 'EEZ' clause excluding its use within national carbon accounts. PMID:16930461

  3. Coadsorption of H2O and CO2 on the Martian surface

    NASA Technical Reports Server (NTRS)

    Zent, A. P.

    1987-01-01

    The adsorption of both CO2 and H2O was measured, under conditions of temperature and partial pressure similar to Mars, for a variety of absorbents. Both adsorb at coverages that exceed a monolayer at their respective Martian abundances. Clearly, their simultaneous presence in the Martian atmosphere will result in coadsorption of both at concentrations that may differ greatly from those measured during separate measurements. To the best of our knowledge, no data exists on the coadsorption of both gases. Co-adsorption experiments were begun and pertinent results will be reported. In the meantime the predicted behavior of such a system was mathematically explored as a compliment to the data, and to aid in its eventual interpretation.

  4. Fungal Community Responses to Past and Future Atmospheric CO2 Differ by Soil Type

    PubMed Central

    Ellis, J. Christopher; Fay, Philip A.; Polley, H. Wayne; Jackson, Robert B.

    2014-01-01

    Soils sequester and release substantial atmospheric carbon, but the contribution of fungal communities to soil carbon balance under rising CO2 is not well understood. Soil properties likely mediate these fungal responses but are rarely explored in CO2 experiments. We studied soil fungal communities in a grassland ecosystem exposed to a preindustrial-to-future CO2 gradient (250 to 500 ppm) in a black clay soil and a sandy loam soil. Sanger sequencing and pyrosequencing of the rRNA gene cluster revealed that fungal community composition and its response to CO2 differed significantly between soils. Fungal species richness and relative abundance of Chytridiomycota (chytrids) increased linearly with CO2 in the black clay (P < 0.04, R2 > 0.7), whereas the relative abundance of Glomeromycota (arbuscular mycorrhizal fungi) increased linearly with elevated CO2 in the sandy loam (P = 0.02, R2 = 0.63). Across both soils, decomposition rate was positively correlated with chytrid relative abundance (r = 0.57) and, in the black clay soil, fungal species richness. Decomposition rate was more strongly correlated with microbial biomass (r = 0.88) than with fungal variables. Increased labile carbon availability with elevated CO2 may explain the greater fungal species richness and Chytridiomycota abundance in the black clay soil, whereas increased phosphorus limitation may explain the increase in Glomeromycota at elevated CO2 in the sandy loam. Our results demonstrate that soil type plays a key role in soil fungal responses to rising atmospheric CO2. PMID:25239904

  5. Maximum Drawdown of Atmospheric CO2 due to Biological Uptake in the Ocean and the Ocean Temperature Effect

    NASA Astrophysics Data System (ADS)

    Odalen, M.; Nycander, J.; Oliver, K. I. C.; Nilsson, J.; Brodeau, L.; Ridgwell, A.

    2016-02-01

    During glacials, atmospheric CO2 is significantly lowered; the decrease is about 1/3 or 90 ppm during the last four glacial cycles. Since the ocean reservoir of carbon, and hence the ocean capacity for storing carbon, is substantially larger than the atmospheric and terrestrial counterparts, it is likely that this lowering was caused by ocean processes, drawing the CO2 into the deep ocean. The Southern Ocean circulation and biological efficiency are widely accepted as having played an important part in this CO2 drawdown. However, the relative effects of different processes contributing to this oceanic uptake have not yet been well constrained. In this work, we focus on better constraining two of these processes; 1) the effect of increased efficiency of the biological carbon uptake, and 2) the effect of changes in global mean ocean temperature on the abiotic ocean-atmosphere CO2 equilibrium. By performing ensemble runs using an Earth System Model of Intermediate Complexity (EMIC) we examine the changes in atmospheric pCO2 achieved by 100% nutrient utilization efficiency of biology. The simulations display different ocean circulation patterns and hence different global ocean mean temperatures. By restoring the atmospheric pCO2 to a target value during the spin-up phase, the total carbon content differs between each of the ensemble members. The difference is due to circulation having direct effects on biology, but also on global ocean mean temperature, changing the solubility of CO2. This study reveals the relative importance of of the processes 1 and 2 (mentioned above) for atmospheric pCO2 in a changed climate. The results of this study also show that a difference in carbon content after spin-up can have a significant effect on the drawdown potential of a maximised biological efficiency. Thus, the choice of spin-up characteristics in a model study of climate change CO2 dynamics may significantly affect the outcome of the study.

  6. The impact on atmospheric CO2 of iron fertilization induced changes in the ocean's biological pump

    NASA Astrophysics Data System (ADS)

    Jin, X.; Gruber, N.; Frenzel, H.; Doney, S. C.; McWilliams, J. C.

    2007-10-01

    Using numerical simulations, we quantify the impact of changes in the ocean's biological pump on the air-sea balance of CO2 by fertilizing a small surface patch in the high-nutrient, low-chlorophyll region of the eastern tropical Pacific with iron. Decade-long fertilization experiments are conducted in a basin-scale, eddy-permitting coupled physical biogeochemical ecological model. In contrast to previous studies, we find that most of the dissolved inorganic carbon (DIC) removed from the euphotic zone by the enhanced biological export is replaced by uptake of CO2 from the atmosphere. Atmospheric uptake efficiencies, the ratio of the perturbation in air-sea CO2 flux to the perturbation in export flux across 100 m, are 0.75 to 0.93 in our patch size-scale experiments. The atmospheric uptake efficiency is insensitive to the duration of the experiment. The primary factor controlling the atmospheric uptake efficiency is the vertical distribution of the enhanced biological production. Iron fertilization at the surface tends to induce production anomalies primarily near the surface, leading to high efficiencies. In contrast, mechanisms that induce deep production anomalies (e.g. altered light availability) tend to have a low uptake efficiency, since most of the removed DIC is replaced by lateral and vertical transport and mixing. Despite high atmospheric uptake efficiencies, patch-scale iron fertilization of the ocean's biological pump tends to remove little CO2 from the atmosphere over the decadal timescale considered here.

  7. The impact on atmospheric CO2 of iron fertilization induced changes in the ocean's biological pump

    NASA Astrophysics Data System (ADS)

    Jin, X.; Gruber, N.; Frenzel, H.; Doney, S. C.; McWilliams, J. C.

    2008-03-01

    Using numerical simulations, we quantify the impact of changes in the ocean's biological pump on the air-sea balance of CO2 by fertilizing a small surface patch in the high-nutrient, low-chlorophyll region of the eastern tropical Pacific with iron. Decade-long fertilization experiments are conducted in a basin-scale, eddy-permitting coupled physical/biogeochemical/ecological model. In contrast to previous studies, we find that most of the dissolved inorganic carbon (DIC) removed from the euphotic zone by the enhanced biological export is replaced by uptake of CO2 from the atmosphere. Atmospheric uptake efficiencies, the ratio of the perturbation in air-sea CO2 flux to the perturbation in export flux across 100 m, integrated over 10 years, are 0.75 to 0.93 in our patch size-scale experiments. The atmospheric uptake efficiency is insensitive to the duration of the experiment. The primary factor controlling the atmospheric uptake efficiency is the vertical distribution of the enhanced biological production and export. Iron fertilization at the surface tends to induce production anomalies primarily near the surface, leading to high efficiencies. In contrast, mechanisms that induce deep production anomalies (e.g. altered light availability) tend to have a low uptake efficiency, since most of the removed DIC is replaced by lateral and vertical transport and mixing. Despite high atmospheric uptake efficiencies, patch-scale iron fertilization of the ocean's biological pump tends to remove little CO2 from the atmosphere over the decadal timescale considered here.

  8. Airborne 2-Micron Double Pulsed Direct Detection IPDA Lidar for Atmospheric CO2 Measurement

    NASA Technical Reports Server (NTRS)

    Yu, Jirong; Petros, Mulugeta; Refaat, Tamer F.; Reithmaier, Karl; Remus, Ruben; Singh, Upendra; Johnson, Will; Boyer, Charlie; Fay, James; Johnston, Susan; hide

    2015-01-01

    An airborne 2-micron double-pulsed Integrated Path Differential Absorption (IPDA) lidar has been developed for atmospheric CO2 measurements. This new 2-miron pulsed IPDA lidar has been flown in spring of 2014 for total ten flights with 27 flight hours. It provides high precision measurement capability by unambiguously eliminating contamination from aerosols and clouds that can bias the IPDA measurement.

  9. Atmospheric CO2 Concentrations from Aircraft for 1972-1981, CSIRO Monitoring Program

    DOE Data Explorer

    Beardsmore, David J. [Commonwealth Scientific and Industrial Research Organization (CSIRO), Victoria, Australia; Pearman, Graeme I. [Commonwealth Scientific and Industrial Research Organization (CSIRO), Victoria, Australia

    2012-01-01

    From 1972 through 1981, air samples were collected in glass flasks from aircraft at a variety of latitudes and altitudes over Australia, New Zealand, and Antarctica. The samples were analyzed for CO2 concentrations with nondispersive infrared gas analysis. The resulting data contain the sampling dates, type of aircraft, flight number, flask identification number, sampling time, geographic sector, distance in kilometers from the listed distance measuring equipment (DME) station, station number of the radio navigation distance measuring equipment, altitude of the aircraft above mean sea level, sample analysis date, flask pressure, tertiary standards used for the analysis, analyzer used, and CO2 concentration. These data represent the first published record of CO2 concentrations in the Southern Hemisphere expressed in the WMO 1981 CO2 Calibration Scale and provide a precise record of atmospheric CO2 concentrations in the troposphere and lower stratosphere over Australia and New Zealand.

  10. Application of AVHRR vegetation index to study atmosphere-biosphere exchange of CO2: Results from a 3-D tracer transport model

    NASA Technical Reports Server (NTRS)

    Fung, Inez Y.; Tucker, C. J.; Prentice, Katharine C.

    1985-01-01

    The 'normalized difference vegetation indices' (NVI) derived from AVHRR radiances are combined with field data of soil respiration and a global map of net primary productivity to prescribe, for the globe, the seasonal exchange of CO2 between the atmosphere and the terrestrial biosphere. The monthly fluxes of CO2 thus obtained are used as inputs to a 3-D tracer transport model which uses winds generated by a 3-D atmospheric general circulation model to advect CO2 as an inert constituent. Analysis of the 3-D model results shows reasonable agreement between the simulated and observed annual cycles of atmospheric CO2 at the locations of the remote monitoring stations. The application is shown of atmospheric CO2 distributions to calibrate the NVI in terms of carbon fluxes. The approach suggests that the NVI may be used to provide quantitative information about long term and global scale variations of photosynthetic activity and of atmospheric CO2 concentrations provided that variations in the atmospheric circulation and in atmospheric composition are known.

  11. Azole-Anion-Based Aprotic Ionic Liquids: Functional Solvents for Atmospheric CO2 Transformation into Various Heterocyclic Compounds.

    PubMed

    Zhao, Yanfei; Wu, Yunyan; Yuan, Guangfeng; Hao, Leiduan; Gao, Xiang; Yang, Zhenzhen; Yu, Bo; Zhang, Hongye; Liu, Zhimin

    2016-10-06

    The chemical transformation of atmospheric CO 2 is of great significance yet still poses a great challenge. Herein, azole-anion-based aprotic ionic liquids (ILs) were synthesized by the deprotonation of weak proton donors (e.g., 2-methylimidazole, 4-methylimidazole, and 2,4-dimethylimidazole) with tetrabutylphosphonium hydroxide, [Bu 4 P][OH]. We found that these ILs, such as [Bu 4 P][2-MIm], could activate atmospheric CO 2 through the formation of carbamates. The resultant carbamate intermediates could further react with various types of substrate, including propargylic alcohols, 2-aminobenzonitriles, ortho-phenylenediamines, and 2-aminothiophenol, thereby producing α-alkylidene cyclic carbonates, quinazoline-2,4(1 H,3 H)-diones, benzimidazolones, and benzothiazoline, respectively, in moderate-to-good yields. Thus, we have achieved the transformation of CO 2 at atmospheric pressure, and we expect this method to open up new routes for the synthesis of various oxygen-containing heterocyclic compounds under metal-free conditions. © 2016 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  12. Recent widespread tree growth decline despite increasing atmospheric CO2.

    PubMed

    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.

  13. Agroecosystem productivity in a warmer and CO2 enriched atmosphere

    NASA Astrophysics Data System (ADS)

    Bernacchi, Carl; Köhler, Iris; Ort, Donald; Long, Steven; Clemente, Thomas

    2017-04-01

    A number of in-field manipulative experiments have been conducted that address the response of key ecosystem services of major agronomic species to rising CO2. Global warming, however, is inextricably linked to rising greenhouse gases in general, of which CO2 is the most dominant. Therefore, agroecosystem functioning in future conditions requires an understanding of plant responses to both rising CO2 and increased temperatures. Few in-field manipulative experiments have been conducted that supplement both heating and CO2 above background concentrations. Here, the results of six years of experimentation using a coupled Free Air CO2 Enrichment (FACE) technology with variable output infrared heating arrays are reported. The manipulative experiment increased temperatures (+ 3.5˚ C) and CO2 (+ 200 μmol mol-1) above background levels for on two major agronomic crop species grown throughout the world, Zea mays (maize) and Glycine max (soybean). The first phase of this research addresses the response of plant physiological parameters to growth in elevated CO2 and warmer temperatures for maize and soybean grown in an open-air manipulative experiment. The results show that any increase in ecosystem productivity associated with rising CO2 is either similar or is offset by growth at higher temperatures, inconsistent with the perceived benefits of higher CO2 plus warmer temperatures on agroecosystem productivity. The second phase of this research addresses the opportunity to genetically modify soybean to allow for improved productivity under high CO2 and warmer temperatures by increasing a key photosynthetic carbon reduction cycle enzyme, SPBase. The results from this research demonstrates that manipulation of the photosynthetic pathway can lead to higher productivity in high CO2 and temperature relative to the wild-type control soybean. Overall, this research advances the understanding of the physiological responses of two major crops, and the impact on ecosystem services

  14. The Martian climate: Energy balance models with CO2/H2O atmospheres

    NASA Technical Reports Server (NTRS)

    Hoffert, M. I.

    1985-01-01

    Coupled equations are developed for mass and heat transport in a seasonal Mars model with condensation and sublimation of CO2 at the polar caps. Topics covered include physical considerations of planetary as mass and energy balance; effects of phase changes at the surface on mass and heat flux; atmospheric transport and governing equations; and numerical analysis.

  15. High Arctic Forests During the Middle Eocene Supported by ~400 ppm Atmospheric CO2

    NASA Astrophysics Data System (ADS)

    Maxbauer, D. P.; Royer, D. L.; LePage, B. A.

    2013-12-01

    Fossils from Paleogene High Arctic deposits provide some of the clearest evidence for greenhouse climates and offer the potential to improve our understanding of Earth system dynamics in a largely ice-free world. One of the most well-known and exquisitely-preserved middle Eocene (47.9-37.8 Myrs ago) polar forest sites, Napartulik, crops out on eastern Axel Heiberg Island (80 °N), Nunavut, Canada. An abundance of data from Napartulik suggest mean annual temperatures of up to 30 °C warmer than today and atmospheric water loads 2× above current levels. Despite this wealth of paleontological and paleoclimatological data, there are currently no direct constraints on atmospheric CO2 levels for Napartulik or any other polar forest site. Here we apply a new plant gas-exchange model to Metasequoia (dawn redwood) leaves to reconstruct atmospheric CO2 from six fossil forests at Napartulik. Individual reconstructions vary between 405-489 ppm with a site mean of 437 ppm (337-564 ppm at 95% confidence). These estimates represent the first direct constraints on CO2 for polar fossil forests and suggest that the temperate conditions present at Napartulik during the middle Eocene were maintained under CO2 concentrations ~1.6× above pre-industrial levels. Our results strongly support the case that long-term climate sensitivity to CO2 in the past was sometimes high, even during largely ice-free periods, highlighting the need to better understand the climate forcing and feedback mechanisms responsible for this amplification.

  16. Secondary brown carbon - Formation of light-absorbing compounds in atmospheric particulates from selected dicarbonyls and amines

    NASA Astrophysics Data System (ADS)

    Kampf, Christopher; Filippi, Alexander; Hoffmann, Thorsten

    2015-04-01

    One of the main open questions regarding organic compounds in atmospheric chemistry today is related to the formation of optically-active compounds and the occurrence of so called brown carbon (Andreae and Gelencsér, 2006). While organic compounds in ambient fine particles for decades have been assumed to not absorb solar radiation, thus resulting in a net cooling effect on climate (IPCC, 2007), it is now generally accepted that a continuum of light-absorbing carbonaceous species is present in fine aerosols (Pöschl, 2003). In this study, light-absorbing compounds from reactions between dicarbonyl compounds, i.e., glyoxal, methylglyoxal, acetylacetone, 2,3-butanedione, 2,5-hexanedione, and glutaraldehyde, and amine species, i.e., ammonia and glycine, were investigated at atmospherically relevant concentrations in bulk solution experiments mimicking atmospheric particulates. Product analyses were performed using UV/Vis spectrophotometry and (ultra) high performance liquid chromatography coupled to diode array detection and ion trap mass spectrometry (HPLC-DAD-ESI-MS/MS), as well as ultra-high resolution (Orbitrap) mass spectrometry (UHPLC-ESI-HRMS/MS). We demonstrate that light-absorbing compounds are formed from a variety of atmospherically relevant dicarbonyls via particle phase reactions with amine nucleophiles. Single dicarbonyl and mixed dicarbonyl experiments were performed and products were analyzed. The reaction products are suggested to be cyclic nitrogen containing compounds such as imidazoles or dihydropyridines as well as open chain compounds resulting from aldol condensation reactions. Further, the reactive turnover was found to be higher at increasing pH values. The aforementioned processes may be of higher relevance in regions with high aerosol pH, e.g., resulting from high ammonia emissions as for example in northern India (Clarisse et al., 2009). References Andreae, M.O., and Gelencsér, A. (2006): Black carbon or brown carbon? The nature of light-absorbing

  17. Rising atmospheric CO2 lowers food zinc, iron, and protein concentrations

    USDA-ARS?s Scientific Manuscript database

    Dietary deficiencies of zinc and iron are a major global public health problem. Most people who experience these deficiencies depend on agricultural crops for zinc and iron. In this context, the influence of rising concentrations of atmospheric CO2 on the availability of these nutrients from crops i...

  18. Prediction of atmospheric δ 13CO 2 using fossil plant tissues

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    A. Hope Jahren; Arens, Nan Crystal; Harbeson, Stephanie A.

    2008-06-30

    To summarize the content: we presented the results of laboratory experiments designed to quantify the relationship between plant tissue δ 13C and δ 13CO 2 values under varying environmental conditions, including differential pCO 2 ranging from 1 to 3 times today’s levels. As predicted, plants grown under elevated pCO2 showed increased average biomass compared to controls grown at the same temperature. Across a very large range in δ 13Ca (≈ 24 ‰) and pCO 2 (≈ 740 ppmv) we observed a consistent correlation between δ13Ca and δ 13Cp (p<0.001). We show an average isotopic depletion of -25.4 ‰ for above-groundmore » tissue and -23.2 ‰ for below-ground tissue of Raphanus sativus L. relative to the composition of the atmosphere under which it formed. For both above- and below-ground tissue, grown at both ~23 °C and ~29 °C, correlation was strong and significant (r2 ≥ 0.98, p<0.001); variation in pCO 2 level had little or no effect on this relationship.« less

  19. The paper trail of the 13C of atmospheric CO2 since the industrial revolution period

    NASA Astrophysics Data System (ADS)

    Yakir, Dan

    2011-07-01

    The 13C concentration in atmospheric CO2 has been declining over the past 150 years as large quantities of 13C-depleted CO2 from fossil fuel burning are added to the atmosphere. Deforestation and other land use changes have also contributed to the trend. Looking at the 13C variations in the atmosphere and in annual growth rings of trees allows us to estimate CO2 uptake by land plants and the ocean, and assess the response of plants to climate. Here I show that the effects of the declining 13C trend in atmospheric CO2 are recorded in the isotopic composition of paper used in the printing industry, which provides a well-organized archive and integrated material derived from trees' cellulose. 13C analyses of paper from two European and two American publications showed, on average, a - 1.65 ± 1.00‰ trend between 1880 and 2000, compared with - 1.45 and - 1.57‰ for air and tree-ring analyses, respectively. The greater decrease in plant-derived 13C in the paper we tested than in the air is consistent with predicted global-scale increases in plant intrinsic water-use efficiency over the 20th century. Distinct deviations from the atmospheric trend were observed in both European and American publications immediately following the World War II period.

  20. The sensitivity of terrestrial carbon storage to historical climate variability and atmospheric CO2 in the United States

    USGS Publications Warehouse

    Tian, H.; Melillo, J.M.; Kicklighter, D.W.; McGuire, A.D.; Helfrich, J.

    1999-01-01

    We use the Terrestrial Ecosystem Model (TEM, Version 4.1) and the land cover data set of the international geosphere-biosphere program to investigate how increasing atmospheric CO2 concentration and climate variability during 1900-1994 affect the carbon storage of terrestrial ecosystems in the conterminous USA, and how carbon storage has been affected by land-use change. The estimates of TEM indicate that over the past 95 years a combination of increasing atmospheric CO2 with historical temperature and precipitation variability causes a 4.2% (4.3 Pg C) decrease in total carbon storage of potential vegetation in the conterminous US, with vegetation carbon decreasing by 7.2% (3.2 Pg C) and soil organic carbon decreasing by 1.9% (1.1 Pg C). Several dry periods including the 1930s and 1950s are responsible for the loss of carbon storage. Our factorial experiments indicate that precipitation variability alone decreases total carbon storage by 9.5%. Temperature variability alone does not significantly affect carbon storage. The effect of CO2 fertilization alone increases total carbon storage by 4.4%. The effects of increasing atmospheric CO2 and climate variability are not additive. Interactions among CO2, temperature and precipitation increase total carbon storage by 1.1%. Our study also shows substantial year-to-year variations in net carbon exchange between the atmosphere and terrestrial ecosystems due to climate variability. Since the 1960s, we estimate these terrestrial ecosystems have acted primarily as a sink of atmospheric CO2 as a result of wetter weather and higher atmospheric CO2 concentrations. For the 1980s, we estimate the natural terrestrial ecosystems, excluding cropland and urban areas, of the conterminous US have accumulated 78.2 Tg C yr-1 because of the combined effect of increasing atmospheric CO2 and climate variability. For the conterminous US, we estimate that the conversion of natural ecosystems to cropland and urban areas has caused a 18.2% (17

  1. Phloem function: A key to understanding and manipulating plant responses to rising atmospheric [CO2]?

    USDA-ARS?s Scientific Manuscript database

    Increasing atmospheric carbon dioxide concentration ([CO2]) directly stimulates photosynthesis and reduces stomatal conductance in C3 plants. Both of these physiological effects have the potential to alter phloem function at elevated [CO2]. Recent research has clearly established that photosynthetic...

  2. 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

    NASA Technical Reports Server (NTRS)

    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.

  3. Lateral transport of soil carbon and land−atmosphere CO2 flux induced by water erosion in China

    PubMed Central

    Yue, Yao; Ni, Jinren; Ciais, Philippe; Piao, Shilong; Wang, Tao; Huang, Mengtian; Borthwick, Alistair G. L.; Li, Tianhong; Wang, Yichu; Chappell, Adrian; Van Oost, Kristof

    2016-01-01

    Soil erosion by water impacts soil organic carbon stocks and alters CO2 fluxes exchanged with the atmosphere. The role of erosion as a net sink or source of atmospheric CO2 remains highly debated, and little information is available at scales larger than small catchments or regions. This study attempts to quantify the lateral transport of soil carbon and consequent land−atmosphere CO2 fluxes at the scale of China, where severe erosion has occurred for several decades. Based on the distribution of soil erosion rates derived from detailed national surveys and soil carbon inventories, here we show that water erosion in China displaced 180 ± 80 Mt C⋅y−1 of soil organic carbon during the last two decades, and this resulted a net land sink for atmospheric CO2 of 45 ± 25 Mt C⋅y−1, equivalent to 8–37% of the terrestrial carbon sink previously assessed in China. Interestingly, the “hotspots,” largely distributed in mountainous regions in the most intensive sink areas (>40 g C⋅m−2⋅y−1), occupy only 1.5% of the total area suffering water erosion, but contribute 19.3% to the national erosion-induced CO2 sink. The erosion-induced CO2 sink underwent a remarkable reduction of about 16% from the middle 1990s to the early 2010s, due to diminishing erosion after the implementation of large-scale soil conservation programs. These findings demonstrate the necessity of including erosion-induced CO2 in the terrestrial budget, hence reducing the level of uncertainty. PMID:27247397

  4. Lateral transport of soil carbon and land-atmosphere CO2 flux induced by water erosion in China

    NASA Astrophysics Data System (ADS)

    Yue, Yao; Ni, Jinren; Ciais, Philippe; Piao, Shilong; Wang, Tao; Huang, Mengtian; Borthwick, Alistair G. L.; Li, Tianhong; Wang, Yichu; Chappell, Adrian; Van Oost, Kristof

    2016-06-01

    Soil erosion by water impacts soil organic carbon stocks and alters CO2 fluxes exchanged with the atmosphere. The role of erosion as a net sink or source of atmospheric CO2 remains highly debated, and little information is available at scales larger than small catchments or regions. This study attempts to quantify the lateral transport of soil carbon and consequent land-atmosphere CO2 fluxes at the scale of China, where severe erosion has occurred for several decades. Based on the distribution of soil erosion rates derived from detailed national surveys and soil carbon inventories, here we show that water erosion in China displaced 180 ± 80 Mt Cṡy-1 of soil organic carbon during the last two decades, and this resulted a net land sink for atmospheric CO2 of 45 ± 25 Mt Cṡy-1, equivalent to 8-37% of the terrestrial carbon sink previously assessed in China. Interestingly, the “hotspots,” largely distributed in mountainous regions in the most intensive sink areas (>40 g Cṡm-2ṡy-1), occupy only 1.5% of the total area suffering water erosion, but contribute 19.3% to the national erosion-induced CO2 sink. The erosion-induced CO2 sink underwent a remarkable reduction of about 16% from the middle 1990s to the early 2010s, due to diminishing erosion after the implementation of large-scale soil conservation programs. These findings demonstrate the necessity of including erosion-induced CO2 in the terrestrial budget, hence reducing the level of uncertainty.

  5. Mechanisms of glacial-to-future atmospheric CO2 effects on plant immunity.

    PubMed

    Williams, Alex; Pétriacq, Pierre; Schwarzenbacher, Roland E; Beerling, David J; Ton, Jurriaan

    2018-04-01

    The impacts of rising atmospheric CO 2 concentrations on plant disease have received increasing attention, but with little consensus emerging on the direct mechanisms by which CO 2 shapes plant immunity. Furthermore, the impact of sub-ambient CO 2 concentrations, which plants have experienced repeatedly over the past 800 000 yr, has been largely overlooked. A combination of gene expression analysis, phenotypic characterisation of mutants and mass spectrometry-based metabolic profiling was used to determine development-independent effects of sub-ambient CO 2 (saCO 2 ) and elevated CO 2 (eCO 2 ) on Arabidopsis immunity. Resistance to the necrotrophic Plectosphaerella cucumerina (Pc) was repressed at saCO 2 and enhanced at eCO 2 . This CO 2 -dependent resistance was associated with priming of jasmonic acid (JA)-dependent gene expression and required intact JA biosynthesis and signalling. Resistance to the biotrophic oomycete Hyaloperonospora arabidopsidis (Hpa) increased at both eCO 2 and saCO 2 . Although eCO 2 primed salicylic acid (SA)-dependent gene expression, mutations affecting SA signalling only partially suppressed Hpa resistance at eCO 2 , suggesting additional mechanisms are involved. Induced production of intracellular reactive oxygen species (ROS) at saCO 2 corresponded to a loss of resistance in glycolate oxidase mutants and increased transcription of the peroxisomal catalase gene CAT2, unveiling a mechanism by which photorespiration-derived ROS determined Hpa resistance at saCO 2 . By separating indirect developmental impacts from direct immunological effects, we uncover distinct mechanisms by which CO 2 shapes plant immunity and discuss their evolutionary significance. © 2018 The Authors. New Phytologist © 2018 New Phytologist Trust.

  6. Scaling laws for perturbations in the ocean-atmosphere system following large CO2 emissions

    NASA Astrophysics Data System (ADS)

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

    2015-07-01

    Scaling relationships are found for perturbations to atmosphere and ocean variables from large transient CO2 emissions. Using the Long-term Ocean-atmosphere-Sediment CArbon cycle Reservoir (LOSCAR) model (Zeebe et al., 2009; Zeebe, 2012b), we calculate perturbations to atmosphere temperature, total carbon, ocean temperature, total ocean carbon, pH, alkalinity, marine-sediment carbon, and carbon-13 isotope anomalies in the ocean and atmosphere resulting from idealized CO2 emission events. The peak perturbations in the atmosphere and ocean variables are then fit to power law functions of the form of γ DαEβ, where D is the event duration, E is its total carbon emission, and γ is a coefficient. Good power law fits are obtained for most system variables for E up to 50 000 PgC and D up to 100 kyr. Although all of the peak perturbations increase with emission rate E/D, we find no evidence of emission-rate-only scaling, α + β = 0. Instead, our scaling yields α + β ≃ 1 for total ocean and atmosphere carbon and 0 < α + β < 1 for most of the other system variables.

  7. Atmospheric CO2 Records from Sites in the Main Geophysical Observatory Air Sampling Network (1983 - 1993)

    DOE Data Explorer

    Brounshtein, A. M. [Main Geophysical Observatory, St. Petersburg, Russia; Shaskov, A. A. [Main Geophysical Observatory, St. Petersburg, Russia; Paramonova, N. N. [Main Geophysical Observatory, St. Petersburg, Russia; Privalov, V. I. [Main Geophysical Observatory, St. Petersburg, Russia; Starodubtsev, Y. A. [Main Geophysical Observatory, St. Petersburg, Russia

    1997-01-01

    Air samples were collected from five sites in the Main Geophysical Observatory air sampling network to monitor the atmospheric CO2 from 1983 - 1993. Airwas collected generally four times per month in pairs of 1.5-L stainless steel electropolished flasks with one greaseless stainless steel stopcock. Sampling was performed by opening the stopcock of the flasks, which have been evacuated at the central laboratory at the Main Geophysical Observatory (MGO). The air was not dried during sample collection. Attempts were made to obtain samples when the wind speed was >5 m/s and the wind direction corresponded to the predetermined "clean air" sector. The period of record at Bering Island is too short to identify any long-term trends in atmospheric CO2 concentrations; however, the yearly mean atmospheric CO2 concentration at Bering Island rose from approximately 346 parts per million by volume (ppmv) in 1986 to 362.6 ppmv in 1993. Measurements from this station are considered indicative of maritime air masses. The period of record at Kotelny Island is too short to identify any long-term trends in atmospheric CO2 concentrations; however, the yearly mean atmospheric CO2 concentration at Kotelny Island rose from 356.08 parts per million by volume (ppmv) in 1988 to 358.8 ppmv in 1993. Because Kotelny Island is the northernmost Russian sampling site, measurements from this site serve as a useful comparison to other northern sites (e.g., Alert, Northwest Territories). In late 1989, air sampling began at the Russian site of Kyzylcha, located in the Republic of Uzbekistan. Unfortunately, the desert site at Kyzylcha has been out of operation since mid-1991 due to financial difficulties in Russia. The annual mean value of 359.02 parts per million by volume (ppmv) for 1990, the lone full year of operation, is higher than measurements from other monitoring programs at this latitude [e.g., Niwot Ridge (354.7 ppmv in 1990) and Tae-ahn Peninsula]. Station "C," an open ocean site, in the

  8. Upscaling nitrogen-mycorrhizal effects to quantify CO2 fertilization.

    NASA Astrophysics Data System (ADS)

    Terrer, C.; Franklin, O.; Kaiser, C.; Vicca, S.; Stocker, B.; Prentice, I. C.; Soudzilovskaia, N.

    2016-12-01

    Terrestrial ecosystems sequester annually about a quarter of anthropogenic carbon dioxide (CO2) emissions. However, it has been proposed that nitrogen (N) availability will limit plants' capacity to absorb increasing quantities of CO2 in the atmosphere. Experiments in which plants are fumigated with elevated CO2 show contrasting results, leaving open the debate of whether the magnitude of the CO2 fertilization effect will be limited by N. By synthesizing data from CO2 experiments through meta-analysis, we found that the magnitude of the CO2 fertilization effect can be explained based on the interaction between N availability and type of mycorrhizal association. Indeed, N availability is the most important driver of the CO2 fertilization effect, however, plants that associate with ectomycorrhizal fungi can overcome N limitations and grow about 30% more under 650ppm than under 400ppm of atmospheric CO2. On the other hand, plants that associate with arbuscular mycorrhizal fungi show no CO2 fertilization effect under low N availability. Using this framework, we quantified biomass responses to CO2 as a function of the soil parameters that determine N availability for the two mycorrhizal types. Then, by overlaying the distribution of mycorrhizal plants with global projections of the soil parameters that determine N availability, we estimated the amount of extra CO2 that terrestrial plants can sequester in biomass for an increase in CO2, as well as the distribution of the CO2 fertilization effect. This synthesis reconciles contrasting views of the role of N in terrestrial carbon uptake and emphasizes the plant control on N availability through interaction with ectomycorrhizal fungi. Large-scale ecosystem models should account for the influence of nitrogen and mycorrhizae reported here, which will improve representation of the CO2 fertilization effect, critical for projecting ecosystem responses and feedbacks to climate change.

  9. Seasonal and interannual variations of atmospheric CO2 and climate

    USGS Publications Warehouse

    Dettinger, M.D.; Ghil, M.

    1998-01-01

    Interannual variations of atmospheric CO2 concentrations at Mauna Loa are almost masked by the seasonal cycle and a strong trend; at the South Pole, the seasonal cycle is small and is almost lost in the trend and interannual variations. Singular-spectrum analysis (SSA) issued here to isolate and reconstruct interannual signals at both sites and to visualize recent decadal changes in the amplitude and phase of the seasonal cycle. Analysis of the Mauna Loa CO2 series illustrates a hastening of the CO2 seasonal cycle, a close temporal relation between Northern Hemisphere (NH) mean temperature trends and the amplitude of the seasonal CO2 cycle, and tentative ties between the latter and seasonality changes in temperature over the NH continents. Variations of the seasonal CO2 cycle at the South Pole differ from those at Mauna Loa: it is phase changes of the seasonal cycle at the South Pole, rather than amplitude changes, that parallel hemispheric and global temperature trends. The seasonal CO2 cycles exhibit earlier occurrences of the seasons by 7 days at Mauna Loa and 18 days at the South Pole. Interannual CO2 variations are shared at the two locations, appear to respond to tropical processes, and can be decomposed mostly into two periodicities, around (3 years)-1 and (4 years)-1, respectively. Joint SSA analyses of CO2 concentrations and tropical climate indices isolate a shared mode with a quasi-triennial (QT) period in which the CO2 and sea-surface temperature (SST) participation are in phase opposition. The other shared mode has a quasi-quadrennial (QQ) period and CO2 variations are in phase with the corresponding tropical SST variations throughout the tropics. Together these interannual modes exhibit a mean lag between tropical SSTs and CO2 variations of about 6-8 months, with SST leading. Analysis of the QT and QQ signals in global gridded SSTs, joint SSA of CO2 and ??13C isotopic ratios, and SSA of CO2 and NH-land temperatures indicate that the QT variations in

  10. Three-dimensional variations of atmospheric CO2: aircraft measurements and multi-transport model simulations

    NASA Astrophysics Data System (ADS)

    Niwa, Y.; Patra, P. K.; Sawa, Y.; Machida, T.; Matsueda, H.; Belikov, D.; Maki, T.; Ikegami, M.; Imasu, R.; Maksyutov, S.; Oda, T.; Satoh, M.; Takigawa, M.

    2011-04-01

    Numerical simulation and validation of three-dimensional structure of atmospheric carbon dioxide (CO2) is necessary for quantification of transport model uncertainty and its role on surface flux estimation by inverse modeling. Simulations of atmospheric CO2 were performed using four transport models and two sets of surface fluxes compared with an aircraft measurement dataset of Comprehensive Observation Network for Trace gases by AIrLiner (CONTRAIL), covering various latitudes, longitudes, and heights. Under this transport model intercomparison project, spatiotemporal variations of CO2 concentration for 2006-2007 were analyzed with a three-dimensional perspective. Results show that the models reasonably simulated vertical profiles and seasonal variations not only over northern latitude areas but also over the tropics and southern latitudes. From CONTRAIL measurements and model simulations, intrusion of northern CO2 in to the Southern Hemisphere, through the upper troposphere, was confirmed. Furthermore, models well simulated the vertical propagation of seasonal variation in the northern free-troposphere. However, significant model-observation discrepancies were found in Asian regions, which are attributable to uncertainty of the surface CO2 flux data. The models consistently underestimated the north-tropics mean gradient of CO2 both in the free-troposphere and marine boundary layer during boreal summer. This result suggests that the north-tropics contrast of annual mean net non-fossil CO2 flux should be greater than 2.7 Pg C yr-1 for 2007.

  11. Reducing the cost of Ca-based direct air capture of CO2.

    PubMed

    Zeman, Frank

    2014-10-07

    Direct air capture, the chemical removal of CO2 directly from the atmosphere, may play a role in mitigating future climate risk or form the basis of a sustainable transportation infrastructure. The current discussion is centered on the estimated cost of the technology and its link to "overshoot" trajectories, where atmospheric CO2 levels are actively reduced later in the century. The American Physical Society (APS) published a report, later updated, estimating the cost of a one million tonne CO2 per year air capture facility constructed today that highlights several fundamental concepts of chemical air capture. These fundamentals are viewed through the lens of a chemical process that cycles between removing CO2 from the air and releasing the absorbed CO2 in concentrated form. This work builds on the APS report to investigate the effect of modifications to the air capture system based on suggestions in the report and subsequent publications. The work shows that reduced carbon electricity and plastic packing materials (for the contactor) may have significant effects on the overall price, reducing the APS estimate from $610 to $309/tCO2 avoided. Such a reduction does not challenge postcombustion capture from point sources, estimated at $80/tCO2, but does make air capture a feasible alternative for the transportation sector and a potential negative emissions technology. Furthermore, air capture represents atmospheric reductions rather than simply avoided emissions.

  12. TES/Aura L2 Carbon Dioxide (CO2) Nadir V7 (TL2CO2N)

    Atmospheric Science Data Center

    2018-01-18

    ... TES/Aura L2 Carbon Dioxide (CO2) Nadir (TL2CO2N) News:  TES News Join TES News List Project ... TES Order Tool Parameters:  Earth Science Atmosphere Atmospheric Chemistry/Carbon and Hydrocarbon Compounds ...

  13. Atmospheric CO2 Records from Sites in the Atmospheric Environment Service Air Sampling Network (1975 and 1994)

    DOE Data Explorer

    Trivett, N. B.A. [Atmospheric Environment Service, Downsview, Ontario, Canada; Hudec, V. C. [Atmospheric Environment Service, Downsview, Ontario, Canada; Wong, C. S. [Marine Carbon Research Centre, Institute of Ocean Sciences, Sidney, British Columbia, Canada

    1997-01-01

    From the mid-1970s through the mid-1990s, air samples were collected for the purposes of monitoring atmospheric CO2 from four sites in the AES air sampling network. Air samples were collected approximately once per week, between 12:00 and 16:00 local time, in a pair of evacuated 2-L thick-wall borosilicate glass flasks. Samples were collected under preferred conditions of wind speed and direction (i.e., upwind of the main station and when winds are strong and steady). The flasks were evacuated to pressures of ~1 × 10-4 mbar or 0.01 Pa prior to being sent to the stations. The airwas not dried during sample collection. The flask data from Alert show an increase in the annual atmospheric CO2 concentration from 341.35 parts per million by volume (ppmv) in 1981 to 357.21 ppmv in 1991. For Cape St. James, Trivett and Higuchi (1989) reported that the mean annual rate of increase, obtained from the slope of a least-squares regression line through the annual averages, was 1.43 ppmv per year. In August 1992, the weather station at Cape St. James was automated; as a result, the flask sampling program was discontinued at this site. Estevan Point, on the West Coast of Vancouver Island, was chosen as a replacement station. Sampling at Estevan Point started in 1992; thus, the monthly and annual CO2record from Estevan Point is too short to show any long-term trends. The sampling site at Sable Island, off the coast of Nova Scotia, was established in 1975. The flask data from Sable Island show an increase in the annual atmospheric CO2 concentration from 334.49 parts per million by volume (ppmv) in 1977 (the first full year of data) to 356.02 ppmv in 1990. For Sable Island, Trivett and Higuchi (1989) reported that the mean annual rate of increase, obtained from the slope of a least-squares regression line through the annual averages, was 1.48 ppmv per year.

  14. Recent Widespread Tree Growth Decline Despite Increasing Atmospheric CO2

    PubMed Central

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

    2010-01-01

    Background The synergetic effects of recent rising atmospheric CO2 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. Methodology/Principal Findings 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° 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. Conclusions 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. PMID:20657763

  15. Phytochemical changes in leaves of subtropical grasses and fynbos shrubs at elevated atmospheric CO 2 concentrations

    NASA Astrophysics Data System (ADS)

    Hattas, D.; Stock, W. D.; Mabusela, W. T.; Green, I. R.

    2005-07-01

    The effects of elevated atmospheric CO 2 concentrations on plant polyphenolic, tannin, nitrogen, phosphorus and total nonstructural carbohydrate concentrations were investigated in leaves of subtropical grass and fynbos shrub species. The hypothesis tested was that carbon-based secondary compounds would increase when carbon gain is in excess of growth requirements. This premise was tested in two ecosystems involving plants with different photosynthetic mechanisms and growth strategies. The first ecosystem comprised grasses from a C 4-dominated, subtropical grassland, where three plots were subjected to three different free air CO 2 enrichment treatments, i.e., elevated (600 to 800 μmol mol -1), intermediate (400 μmol mol -1) and ambient atmospheric CO 2. One of the seven grass species, Alloteropsis semialata, had a C 3 photosynthetic pathway while the other grasses were all C 4. The second ecosystem was simulated in a microcosm experiment where three fynbos species were grown in open-top chambers at ambient and 700 μmol mol -1 atmospheric CO 2 in low nutrient acid sands typical of south western coastal and mountain fynbos ecosystems. Results showed that polyphenolics and tannins did not increase in the grass species under elevated CO 2 and only in Leucadendron laureolum among the fynbos species. Similarly, foliar nitrogen content of grasses was largely unaffected by elevated CO 2, and among the fynbos species, only L. laureolum and Leucadendron xanthoconus showed changes in foliar nitrogen content under elevated CO 2, but these were of different magnitude. The overall decrease in nitrogen and phosphorus and consequent increase in C:N and C:P ratio in both ecosystems, along with the increase in polyphenolics and tannins in L. laureolum in the fynbos ecosystem, may negatively affect forage quality and decomposition rates. It is concluded that fast growing grasses do not experience sink limitation and invest extra carbon into growth rather than polyphenolics and

  16. Measurement of Atmospheric CO2 Column Concentrations to Cloud Tops With a Pulsed Multi-Wavelength Airborne Lidar

    NASA Technical Reports Server (NTRS)

    Mao, Jianping; Ramanathan, Anand; Abshire, James B.; Kawa, Stephan R.; Riris, Haris; Allan, Graham R.; Rodriguez, Michael R.; Hasselbrack, William E.; Sun, Xiaoli; Numata, Kenji; hide

    2018-01-01

    We have measured the column-averaged atmospheric CO2 mixing ratio to a variety of cloud tops by using an airborne pulsed multi-wavelength integrated-path differential absorption (IPDA) lidar. Airborne measurements were made at altitudes up to 13 km during the 2011, 2013 and 2014 NASA Active Sensing of CO2 Emissions over Nights, Days, and Seasons (ASCENDS) science campaigns flown in the United States West and Midwest and were compared to those from an in situ sensor. Analysis of the lidar backscatter profiles shows the average cloud top reflectance was approx. 5% for the CO2 measurement at 1572.335 nm except to cirrus clouds, which had lower reflectance. The energies for 1 micro-s wide laser pulses reflected from cloud tops were sufficient to allow clear identification of CO2 absorption line shape and then to allow retrievals of atmospheric column CO2 from the aircraft to cloud tops more than 90% of the time. Retrievals from the CO2 measurements to cloud tops had minimal bias but larger standard deviations when compared to those made to the ground, depending on cloud top roughness and reflectance. The measurements show this new capability helps resolve CO2 horizontal and vertical gradients in the atmosphere. When used with nearby full-column measurements to ground, the CO2 measurements to cloud tops can be used to estimate the partial-column CO2 concentration below clouds, which should lead to better estimates of surface carbon sources and sinks. This additional capability of the range-resolved CO2 IPDA lidar technique provides a new benefit for studying the carbon cycle in future airborne and space-based CO2 missions.

  17. Measurement of atmospheric CO2 column concentrations to cloud tops with a pulsed multi-wavelength airborne lidar

    NASA Astrophysics Data System (ADS)

    Mao, Jianping; Ramanathan, Anand; Abshire, James B.; Kawa, Stephan R.; Riris, Haris; Allan, Graham R.; Rodriguez, Michael; Hasselbrack, William E.; Sun, Xiaoli; Numata, Kenji; Chen, Jeff; Choi, Yonghoon; Yang, Mei Ying Melissa

    2018-01-01

    We have measured the column-averaged atmospheric CO2 mixing ratio to a variety of cloud tops by using an airborne pulsed multi-wavelength integrated-path differential absorption (IPDA) lidar. Airborne measurements were made at altitudes up to 13 km during the 2011, 2013 and 2014 NASA Active Sensing of CO2 Emissions over Nights, Days, and Seasons (ASCENDS) science campaigns flown in the United States West and Midwest and were compared to those from an in situ sensor. Analysis of the lidar backscatter profiles shows the average cloud top reflectance was ˜ 5 % for the CO2 measurement at 1572.335 nm except to cirrus clouds, which had lower reflectance. The energies for 1 µs wide laser pulses reflected from cloud tops were sufficient to allow clear identification of CO2 absorption line shape and then to allow retrievals of atmospheric column CO2 from the aircraft to cloud tops more than 90 % of the time. Retrievals from the CO2 measurements to cloud tops had minimal bias but larger standard deviations when compared to those made to the ground, depending on cloud top roughness and reflectance. The measurements show this new capability helps resolve CO2 horizontal and vertical gradients in the atmosphere. When used with nearby full-column measurements to ground, the CO2 measurements to cloud tops can be used to estimate the partial-column CO2 concentration below clouds, which should lead to better estimates of surface carbon sources and sinks. This additional capability of the range-resolved CO2 IPDA lidar technique provides a new benefit for studying the carbon cycle in future airborne and space-based CO2 missions.

  18. Transition Delay in a Hypervelocity Boundary Layer using Nonequilibrium CO2 Injection

    DTIC Science & Technology

    2008-10-28

    flows than for either air or N2 flows. The explanation for this phenomenon lies in the fact that when CO2 is in vibrational and chemical ... chemical non-equilibrium, these relax- ation processes absorb energy from acoustic disturbances whose growth is responsible for transition in high...atmosphere at hypersonic speeds, they must somehow provide for, avoid, or otherwise accommodate the enormous heat-transfer rates to the vehicle engen

  19. Effects of elevated atmospheric CO2 concentrations, clipping regimen and differential day/night atmospheric warming on tissue nitrogen concentrations of a perennial pasture grass

    PubMed Central

    Volder, Astrid; Gifford, Roger M.; Evans, John R.

    2015-01-01

    Forecasting the effects of climate change on nitrogen (N) cycling in pastures requires an understanding of changes in tissue N. We examined the effects of elevated atmospheric CO2 concentration, atmospheric warming and simulated grazing (clipping frequency) on aboveground and belowground tissue N concentrations and C : N ratios of a C3 pasture grass. Phalaris aquatica L. cv. ‘Holdfast’ was grown in the field in six transparent temperature gradient tunnels (18 × 1.5 × 1.5 m each), three at ambient atmospheric CO2 and three at 759 p.p.m. CO2. Within each tunnel, there were three air temperature treatments: ambient control, +2.2/+4.0 °C above ambient day/night warming and +3.0 °C continuous warming. A frequent and an infrequent clipping treatment were applied to each warming × CO2 combination. Green leaf N concentrations were decreased by elevated CO2 and increased by more frequent clipping. Both warming treatments increased leaf N concentrations under ambient CO2 concentrations, but did not significantly alter leaf N concentrations under elevated CO2 concentrations. Nitrogen resorption from leaves was decreased under elevated CO2 conditions as well as by more frequent clipping. Fine root N concentrations decreased strongly with increasing soil depth and were further decreased at the 10–60 cm soil depths by elevated CO2 concentrations. The interaction between the CO2 and warming treatments showed that leaf N concentration was affected in a non-additive manner. Changes in leaf C : N ratios were driven by changes in N concentration. Overall, the effects of CO2, warming and clipping treatments on aboveground tissue N concentrations were much greater than on belowground tissue. PMID:26272874

  20. Enhanced terrestrial carbon uptake: global drivers and implications for the growth rate of atmospheric CO2.

    NASA Astrophysics Data System (ADS)

    Keenan, Trevor F.; Prentice, Colin; Canadell, Josep; Williams, Christopher; Han, Wang; Riley, William; Zhu, Qing; Koven, Charlie; Chambers, Jeff

    2017-04-01

    In this presentation we will focus on using decadal changes in the global carbon cycle to better understand how ecosystems respond to changes in CO2 concentration, temperature, and water and nutrient availability. Using global carbon budget estimates, ground, atmospheric and satellite observations, and multiple process-based global vegetation models, we examine the causes and consequences of the long-term changes in the terrestrial carbon sink. We show that over the past century the sink has been greatly enhanced, largely due to the effect of elevated CO2 on photosynthesis dominating over warming induced increases in respiration. We also examine the relative roles of greening, water and nutrients, along with individual events such as El Nino. We show that a slowdown in the rate of warming over land since the start of the 21st century likely led to a large increase in the sink, and that this increase was sufficient to lead to a pause in the growth rate of atmospheric CO2. We also show that the recent El Nino resulted in the highest growth rate of atmospheric CO2 ever recorded. Our results provide evidence of the relative roles of CO2 fertilization and warming induced respiration in the global carbon cycle, along with an examination of the impact of climate extremes.

  1. Practical method of CO.sub.2 sequestration

    DOEpatents

    Goswami, D Yogi [Gainesville, FL; Lee, Man Su [Houston, TX; Kothurkar, Nikhil K [Tampa, FL; Stefanakos, Elias K [Tampa, FL

    2011-03-01

    A process and device to capture of CO.sub.2 at its originating source, such as a power plant, is disclosed. Absorbent material is recharged by desorbing CO.sub.2, so that it may be sequestered or used in another application. Continual recharging results in loss of absorbent surface area, due to pore plugging and sintering of particles. Calcium oxide or calcium hydroxide was immobilized to a fibrous ceramic-based fabric substrate as a thin film and sintered, creating an absorbent material. The samples were characterized, showing continuous cyclic carbonation conversions between about 62% and 75% under mild calcination conditions at 750.degree. C. and no CO.sub.2 in N.sub.2. Under the more severe calcination condition at 850.degree. C. and 20 wt % CO.sub.2 in N.sub.2, yttria fabric was superior to alumina as a substrate for carbon dioxide capture and the reactivity of the calcium oxide absorbent immobilized to yttria was maintained at the same level in the 12 cycles.

  2. Atmospheric CO and hydrogen uptake and CO oxidizer phylogeny for miyake-jima, Japan volcanic deposits.

    PubMed

    King, Gary M; Weber, Carolyn F; Nanba, Kenji; Sato, Yoshinori; Ohta, Hiroyuki

    2008-01-01

    We have assayed rates of atmospheric CO and hydrogen uptake, maximum potential CO uptake and the major phylogenetic composition of CO-oxidizing bacterial communities for a variety of volcanic deposits on Miyake-jima, Japan. These deposits represented different ages and stages of plant succession, ranging from unvegetated scoria deposited in 1983 to forest soils on deposits >800 yr old. Atmospheric CO and hydrogen uptake rates varied from -2.0±1.8-6.3±0.1 mg CO m(-2) d(-1) and 0.0±0.4-2.0±0.2 mg H(2) m(-2) d(-1), respectively, and were similar to or greater than values reported for sites on Kilauea volcano, Hawaii, USA. At one of the forested sites, CO was emitted to the atmosphere, while two vegetated sites did not consume atmospheric hydrogen, an unusual observation. Although maximum potential CO uptake rates were also comparable to values for Kilauea, the relationship between these rates and organic carbon contents of scoria or soil indicated that CO oxidizers were relatively more abundant in Miyake-jima deposits. Phylogenetic analyses based on the large sub-unit gene for carbon monoxide dehydrogenase (coxL) indicated that many novel lineages were present on Miyake-jima, that CO-oxidizing Proteobacteria were prevalent in vegetated sites and that community structure appeared to vary more than composition among sites.

  3. The Effect of Thermal Convection on Earth-Atmosphere CO2 Gas Exchange in Aggregated Soil

    NASA Astrophysics Data System (ADS)

    Ganot, Y.; Weisbrod, N.; Dragila, M. I.

    2011-12-01

    Gas transport in soils and surface-atmosphere gas exchange are important processes that affect different aspects of soil science such as soil aeration, nutrient bio-availability, sorption kinetics, soil and groundwater pollution and soil remediation. Diffusion and convection are the two main mechanisms that affect gas transport, fate and emissions in the soils and in the upper vadose zone. In this work we studied CO2 soil-atmosphere gas exchange under both day-time and night-time conditions, focusing on the impact of thermal convection (TCV) during the night. Experiments were performed in a climate-controlled laboratory. One meter long columns were packed with matrix of different grain size (sand, gravel and soil aggregates). Air with 2000 ppm CO2 was injected into the bottom of the columns and CO2 concentration within the columns was continuously monitored by an Infra Red Gas Analyzer. Two scenarios were compared for each soil: (1) isothermal conditions, representing day time conditions; and (2) thermal gradient conditions, i.e., atmosphere colder than the soil, representing night time conditions. Our results show that under isothermal conditions, diffusion is the major mechanism for surface-atmosphere gas exchange for all grain sizes; while under night time conditions the prevailing mechanism is dependent on the air permeability of the matrix: for sand and gravel it is diffusion, and for soil aggregates it is TCV. Calculated CO2 flux for the soil aggregates column shows that the TCV flux was three orders of magnitude higher than the diffusive flux.

  4. Antarctic ice sheet sensitivity to atmospheric CO2 variations in the early to mid-Miocene

    NASA Astrophysics Data System (ADS)

    Levy, Richard; Harwood, David; Florindo, Fabio; Sangiorgi, Francesca; Tripati, Robert; von Eynatten, Hilmar; Gasson, Edward; Kuhn, Gerhard; Tripati, Aradhna; DeConto, Robert; Fielding, Christopher; Field, Brad; Golledge, Nicholas; McKay, Robert; Naish, Timothy; Olney, Matthew; Pollard, David; Schouten, Stefan; Talarico, Franco; Warny, Sophie; Willmott, Veronica; Acton, Gary; Panter, Kurt; Paulsen, Timothy; Taviani, Marco; SMS Science Team; Acton, Gary; Askin, Rosemary; Atkins, Clifford; Bassett, Kari; Beu, Alan; Blackstone, Brian; Browne, Gregory; Ceregato, Alessandro; Cody, Rosemary; Cornamusini, Gianluca; Corrado, Sveva; DeConto, Robert; Del Carlo, Paola; Di Vincenzo, Gianfranco; Dunbar, Gavin; Falk, Candice; Field, Brad; Fielding, Christopher; Florindo, Fabio; Frank, Tracy; Giorgetti, Giovanna; Grelle, Thomas; Gui, Zi; Handwerger, David; Hannah, Michael; Harwood, David M.; Hauptvogel, Dan; Hayden, Travis; Henrys, Stuart; Hoffmann, Stefan; Iacoviello, Francesco; Ishman, Scott; Jarrard, Richard; Johnson, Katherine; Jovane, Luigi; Judge, Shelley; Kominz, Michelle; Konfirst, Matthew; Krissek, Lawrence; Kuhn, Gerhard; Lacy, Laura; Levy, Richard; Maffioli, Paola; Magens, Diana; Marcano, Maria C.; Millan, Cristina; Mohr, Barbara; Montone, Paola; Mukasa, Samuel; Naish, Timothy; Niessen, Frank; Ohneiser, Christian; Olney, Mathew; Panter, Kurt; Passchier, Sandra; Patterson, Molly; Paulsen, Timothy; Pekar, Stephen; Pierdominici, Simona; Pollard, David; Raine, Ian; Reed, Joshua; Reichelt, Lucia; Riesselman, Christina; Rocchi, Sergio; Sagnotti, Leonardo; Sandroni, Sonia; Sangiorgi, Francesca; Schmitt, Douglas; Speece, Marvin; Storey, Bryan; Strada, Eleonora; Talarico, Franco; Taviani, Marco; Tuzzi, Eva; Verosub, Kenneth; von Eynatten, Hilmar; Warny, Sophie; Wilson, Gary; Wilson, Terry; Wonik, Thomas; Zattin, Massimiliano

    2016-03-01

    Geological records from the Antarctic margin offer direct evidence of environmental variability at high southern latitudes and provide insight regarding ice sheet sensitivity to past climate change. The early to mid-Miocene (23-14 Mya) is a compelling interval to study as global temperatures and atmospheric CO2 concentrations were similar to those projected for coming centuries. Importantly, this time interval includes the Miocene Climatic Optimum, a period of global warmth during which average surface temperatures were 3-4 °C higher than today. Miocene sediments in the ANDRILL-2A drill core from the Western Ross Sea, Antarctica, indicate that the Antarctic ice sheet (AIS) was highly variable through this key time interval. A multiproxy dataset derived from the core identifies four distinct environmental motifs based on changes in sedimentary facies, fossil assemblages, geochemistry, and paleotemperature. Four major disconformities in the drill core coincide with regional seismic discontinuities and reflect transient expansion of grounded ice across the Ross Sea. They correlate with major positive shifts in benthic oxygen isotope records and generally coincide with intervals when atmospheric CO2 concentrations were at or below preindustrial levels (˜280 ppm). Five intervals reflect ice sheet minima and air temperatures warm enough for substantial ice mass loss during episodes of high (˜500 ppm) atmospheric CO2. These new drill core data and associated ice sheet modeling experiments indicate that polar climate and the AIS were highly sensitive to relatively small changes in atmospheric CO2 during the early to mid-Miocene.

  5. Antarctic ice sheet sensitivity to atmospheric CO2 variations in the early to mid-Miocene

    PubMed Central

    Levy, Richard; Harwood, David; Florindo, Fabio; Sangiorgi, Francesca; Tripati, Robert; von Eynatten, Hilmar; Tripati, Aradhna; DeConto, Robert; Fielding, Christopher; Field, Brad; Golledge, Nicholas; McKay, Robert; Naish, Timothy; Olney, Matthew; Pollard, David; Schouten, Stefan; Talarico, Franco; Warny, Sophie; Willmott, Veronica; Acton, Gary; Panter, Kurt; Paulsen, Timothy; Taviani, Marco

    2016-01-01

    Geological records from the Antarctic margin offer direct evidence of environmental variability at high southern latitudes and provide insight regarding ice sheet sensitivity to past climate change. The early to mid-Miocene (23–14 Mya) is a compelling interval to study as global temperatures and atmospheric CO2 concentrations were similar to those projected for coming centuries. Importantly, this time interval includes the Miocene Climatic Optimum, a period of global warmth during which average surface temperatures were 3–4 °C higher than today. Miocene sediments in the ANDRILL-2A drill core from the Western Ross Sea, Antarctica, indicate that the Antarctic ice sheet (AIS) was highly variable through this key time interval. A multiproxy dataset derived from the core identifies four distinct environmental motifs based on changes in sedimentary facies, fossil assemblages, geochemistry, and paleotemperature. Four major disconformities in the drill core coincide with regional seismic discontinuities and reflect transient expansion of grounded ice across the Ross Sea. They correlate with major positive shifts in benthic oxygen isotope records and generally coincide with intervals when atmospheric CO2 concentrations were at or below preindustrial levels (∼280 ppm). Five intervals reflect ice sheet minima and air temperatures warm enough for substantial ice mass loss during episodes of high (∼500 ppm) atmospheric CO2. These new drill core data and associated ice sheet modeling experiments indicate that polar climate and the AIS were highly sensitive to relatively small changes in atmospheric CO2 during the early to mid-Miocene. PMID:26903644

  6. Antarctic ice sheet sensitivity to atmospheric CO2 variations in the early to mid-Miocene.

    PubMed

    Levy, Richard; Harwood, David; Florindo, Fabio; Sangiorgi, Francesca; Tripati, Robert; von Eynatten, Hilmar; Gasson, Edward; Kuhn, Gerhard; Tripati, Aradhna; DeConto, Robert; Fielding, Christopher; Field, Brad; Golledge, Nicholas; McKay, Robert; Naish, Timothy; Olney, Matthew; Pollard, David; Schouten, Stefan; Talarico, Franco; Warny, Sophie; Willmott, Veronica; Acton, Gary; Panter, Kurt; Paulsen, Timothy; Taviani, Marco

    2016-03-29

    Geological records from the Antarctic margin offer direct evidence of environmental variability at high southern latitudes and provide insight regarding ice sheet sensitivity to past climate change. The early to mid-Miocene (23-14 Mya) is a compelling interval to study as global temperatures and atmospheric CO2 concentrations were similar to those projected for coming centuries. Importantly, this time interval includes the Miocene Climatic Optimum, a period of global warmth during which average surface temperatures were 3-4 °C higher than today. Miocene sediments in the ANDRILL-2A drill core from the Western Ross Sea, Antarctica, indicate that the Antarctic ice sheet (AIS) was highly variable through this key time interval. A multiproxy dataset derived from the core identifies four distinct environmental motifs based on changes in sedimentary facies, fossil assemblages, geochemistry, and paleotemperature. Four major disconformities in the drill core coincide with regional seismic discontinuities and reflect transient expansion of grounded ice across the Ross Sea. They correlate with major positive shifts in benthic oxygen isotope records and generally coincide with intervals when atmospheric CO2 concentrations were at or below preindustrial levels (∼280 ppm). Five intervals reflect ice sheet minima and air temperatures warm enough for substantial ice mass loss during episodes of high (∼500 ppm) atmospheric CO2 These new drill core data and associated ice sheet modeling experiments indicate that polar climate and the AIS were highly sensitive to relatively small changes in atmospheric CO2 during the early to mid-Miocene.

  7. Annual mean mixing ratios of N2, Ar, O2, and CO in the martian atmosphere

    NASA Astrophysics Data System (ADS)

    Krasnopolsky, Vladimir A.

    2017-09-01

    The precise mixing ratios of N2, Ar, O2, and CO measured by the MSL Curiosity quadrupole mass spectrometer must be corrected for the seasonal variations of the atmospheric pressure to reproduce annual mean mixing ratios on Mars. The corrections are made using measurements for the first year of the Viking Landers 1 and 2 and the Mars Climate Database data. The mean correction factor is 0.899 ± 0.006 resulting in annual mean mixing ratios of (1.83 ± 0.03)% for N2, (1.86 ± 0.02)% for Ar, (1.56 ± 0.06) × 10-3 for O2, and 673 ± 2.6 ppm for CO. The O2 mixing ratio agrees with the Herschel value within its uncertainty, the ground-based observations corrected for the dust extinction, and photochemical models by Nair et al. (1994) and Krasnopolsky (2010). The CO mixing ratio is in excellent agreement with the MRO/CRISM value of 700 ppm and with 667, 693, and 684 ppm recently observed at LS = 60, 89, and 110° and corrected to the annual mean conditions. Lifetimes of N2 and Ar are very long in the martian atmosphere, and differences between the MSL and Viking data on these species cannot be attributed to their variations.

  8. Changes in Atmospheric CO2 Influence the Allergenicity of Aspergillus fumigatus fungal spore

    NASA Astrophysics Data System (ADS)

    Lang-Yona, N.; Levin, Y.; Dannemoller, K. C.; Yarden, O.; Peccia, J.; Rudich, Y.

    2013-12-01

    Increased allergic susceptibility has been documented without a comprehensive understanding for its causes. Therefore understanding trends and mechanisms of allergy inducing agents is essential. In this study we investigated whether elevated atmospheric CO2 levels can affect the allergenicity of Aspergillus fumigatus, a common allergenic fungal species. Both direct exposure to changing CO2 levels during fungal growth, and indirect exposure through changes in the C:N ratios in the growth media were inspected. We determined the allergenicity of the spores through two types of immunoassays, accompanied with genes expression analysis, and proteins relative quantification. We show that fungi grown under present day CO2 levels (392 ppm) exhibit 8.5 and 3.5 fold higher allergenicity compared to fungi grown at preindustrial (280 ppm) and double (560 ppm) CO2 levels, respectively. A corresponding trend is observed in the expression of genes encoding for known allergenic proteins and in the major allergen Asp f1 concentrations, possibly due to physiological changes such as respiration rates and the nitrogen content of the fungus, influenced by the CO2 concentrations. Increased carbon and nitrogen levels in the growth medium also lead to a significant increase in the allergenicity, for which we propose two different biological mechanisms. We suggest that climatic changes such as increasing atmospheric CO2 levels and changes in the fungal growth medium may impact the ability of allergenic fungi such as Aspergillus fumigatus to induce allergies. The effect of changing CO2 concentrations on the total allergenicity per 10^7 spores of A. fumigatus (A), the major allergen Asp f1 concentration in ng per 10^7 spores (B), and the gene expression by RT-PCR (C). The error bars represent the standard error of the mean.

  9. Inter-annual changes in detritus-based food chains can enhance plant growth response to elevated atmospheric CO2.

    PubMed

    Hines, Jes; Eisenhauer, Nico; Drake, Bert G

    2015-12-01

    Elevated atmospheric CO2 generally enhances plant growth, but the magnitude of the effects depend, in part, on nutrient availability and plant photosynthetic pathway. Due to their pivotal role in nutrient cycling, changes in abundance of detritivores could influence the effects of elevated atmospheric CO2 on essential ecosystem processes, such as decomposition and primary production. We conducted a field survey and a microcosm experiment to test the influence of changes in detritus-based food chains on litter mass loss and plant growth response to elevated atmospheric CO2 using two wetland plants: a C3 sedge (Scirpus olneyi) and a C4 grass (Spartina patens). Our field study revealed that organism's sensitivity to climate increased with trophic level resulting in strong inter-annual variation in detritus-based food chain length. Our microcosm experiment demonstrated that increased detritivore abundance could not only enhance decomposition rates, but also enhance plant growth of S. olneyi in elevated atmospheric CO2 conditions. In contrast, we found no evidence that changes in the detritus-based food chains influenced the growth of S. patens. Considered together, these results emphasize the importance of approaches that unite traditionally subdivided food web compartments and plant physiological processes to understand inter-annual variation in plant production response to elevated atmospheric CO2. © 2015 John Wiley & Sons Ltd.

  10. Apportionment of carbon dioxide over central Europe: insights from combined measurements of atmospheric CO2 mixing ratios and carbon isotope composition

    NASA Astrophysics Data System (ADS)

    Zimnoch, M.; Jelen, D.; Galkowski, M.; Kuc, T.; Necki, J.; Chmura, L.; Gorczyca, Z.; Jasek, A.; Rozanski, K.

    2012-04-01

    The European continent, due to high population density and numerous sources of anthropogenic CO2 emissions, plays an important role in the global carbon budget. Nowadays, precise measurements of CO2 mixing ratios performed by both global and regional monitoring networks, combined with appropriate models of carbon cycle, allow quantification of the European input to the global atmospheric CO2 load. However, measurements of CO2 mixing ratios alone cannot provide the information necessary for the apportionment of fossil-fuel related and biogenic contributions to the total CO2 burden of the regional atmosphere. Additional information is required, for instance obtained through measurements of radiocarbon content in atmospheric carbon dioxide. Radiocarbon is a particularly useful tracer for detecting fossil carbon in the atmosphere on different spatial and temporal scales. Regular observations of atmospheric CO2mixing ratios and their isotope compositions have been performed during the period of 2005-2009 at two sites located in central Europe (southern Poland). The sites, only ca. 100 km apart, represent two extreme environments with respect to the extent of anthropogenic pressure: (i) the city of Krakow, representing typical urban environment with numerous sources of anthropogenic CO2, and (ii) remote mountain site Kasprowy Wierch, relatively free of local influences. Regular, quasi-continuous measurements of CO2 mixing ratios have been performed at both sites. In addition, cumulative samples of atmospheric CO2 have been collected (weekly sampling regime for Krakow and monthly for Kasprowy Wierch) to obtain mean carbon isotope signature (14C/12C and 13C/12C ratios) of atmospheric CO2 at both sampling locations. Partitioning of the local atmospheric CO2 load at both locations has been performed using isotope- and mass balance approach. In Krakow, the average fossil-fuel related contribution to the local atmospheric CO2 load was equal to approximately 3.4%. The biogenic

  11. Characteristics of variations of climate change and atmospheric CO2 concentration at different time scales over the past 500 Ma

    NASA Astrophysics Data System (ADS)

    LIU, Z.; Huang, S. S. X. E. C.; Tang, X.

    2015-12-01

    It is generally believed that current global warming is due to the persistent rise of atmospheric greenhouse gas CO2. The consensus is based mostly on the observational data of past decades and the polar ice core records. To understand the relationship between climate change and atmospheric CO2, their behaviors over a longer interval at different time scales need to be appreciated. Here, we collect and analyze past 500 Ma records of atmospheric CO2 and temperature in six time periods, namely Phanerozoic, Cenozoic, middle Pleistocene, last deglaciation, past millennium, and recent decades. According to the carriers and time spans, we divide these records into three categories: 1.The millionaire and longer records from model calculation and paleosols/paleobotany proxies. Although the trends of both variables are generally consistent on this time scale, it is difficult to establish a clear causal relationship because of great uncertainties and low resolutions of both sets of data. 2.The orbital scale mainly from the polar ice core. High precise CO2 and temperature reconstructions allow for an examination of the possible role of atmospheric CO2 in the glacial-interglacial transformation. 3.The records at centennial and shorter time scales over the past millennium from ice, snow, and instrumental data. The past millennium records are most abundant and accurate, especially CO2 has been measured directly in recent decades. However, due to the difficulties in distinguishing the effect of CO2 from other factors, there are great uncertainties in the interpretation of climate change versus CO2. Overall, we come to the following conclusions:1.Paleoclimatic reconstructions show that both temperature and atmospheric CO2 have generally decreased over the past 500 Ma. However, there are no consistent sequential orders in the changes between these two variables. 2.The Earth's atmospheric CO2 has a drastic oscillation history. There were many high CO2 periods when the values were

  12. Seasonal and interannual variations of atmospheric CO2 and climate

    NASA Astrophysics Data System (ADS)

    Dettinger, Michael D.; Ghil, Michael

    1998-02-01

    Interannual variations of atmospheric CO2 concentrations at Mauna Loa are almost masked by the seasonal cycle and a strong trend; at the South Pole, the seasonal cycle is small and is almost lost in the trend and interannual variations. Singular-spectrum analysis (SSA) is used here to isolate and reconstruct interannual signals at both sites and to visualize recent decadal changes in the amplitude and phase of the seasonal cycle. Analysis of the Mauna Loa CO2 series illustrates a hastening of the CO2 seasonal cycle, a close temporal relation between Northern Hemisphere (NH) mean temperature trends and the amplitude of the seasonal CO2 cycle, and tentative ties between the latter and seasonality changes in temperature over the NH continents. Variations of the seasonal CO2 cycle at the South Pole differ from those at Mauna Loa: it is phase changes of the seasonal cycle at the South Pole, rather than amplitude changes, that parallel hemispheric and global temperature trends. The seasonal CO2 cycles exhibit earlier occurrences of the seasons by 7days at Mauna Loa and 18days at the South Pole. Interannual CO2 variations are shared at the two locations, appear to respond to tropical processes, and can be decomposed mostly into two periodicities, around (3years)-1 and (4years)-1, respectively. Joint SSA analyses of CO2 concentrations and tropical climate indices isolate a shared mode with a quasi-triennial (QT) period in which the CO2 and sea-surface temperature (SST) participation are in phase opposition. The other shared mode has a quasi-quadrennial (QQ) period and CO2 variations are in phase with the corresponding tropical SST variations throughout the tropics. Together these interannual modes exhibit a mean lag between tropical SSTs and CO2 variations of about 6 8months, with SST leading

  13. Elevated atmospheric CO2 negatively impacts photosynthesis through radiative forcing and physiology-mediated climate feedback

    NASA Astrophysics Data System (ADS)

    Zhu, Peng; Zhuang, Qianlai; Ciais, Philippe; Welp, Lisa; Li, Wenyu; Xin, Qinchuan

    2017-02-01

    Increasing atmospheric CO2 affects photosynthesis involving directly increasing leaf carboxylation rates, stomatal closure, and climatic effects. The direct effects are generally thought to be positive leading to increased photosynthesis, while its climatic effects can be regionally positive or negative. These effects are usually considered to be independent from each other, but they are in fact coupled through interactions between land surface exchanges of gases and heat and the physical climate system. In particular, stomatal closure reduces evapotranspiration and increases sensible heat emissions from ecosystems, leading to decreased atmospheric moisture and precipitation and local warming. We use a coupled earth system model to attribute the influence of the increase in CO2 on gross primary productivity (GPP) during the period of 1930-2011. In our model, CO2 radiative effects cause climate change that has only a negligible effect on global GPP (a reduction of 0.9 ± 2% during the last 80 years) because of opposite responses between tropical and northern biomes. On the other hand, CO2 physiological effects on GPP are both positive, by increased carboxylation rates and water use efficiency (7.1 ± 0.48% increase), and negative, by vegetation-climate feedback reducing precipitation, as a consequence of decreased transpiration and increased sensible heat in areas without water limitation (2.7 ± 1.76% reduction).When considering the coupled atmosphere-vegetation system, negative climate feedback on photosynthesis and plant growth due to the current level of CO2 opposes 29-38% of the gains from direct fertilization effects.

  14. Annual mean mixing ratios of N2, Ar, O2, and CO in the martian atmosphere

    NASA Astrophysics Data System (ADS)

    Krasnopolsky, V.

    2017-09-01

    The precise mixing ratios of N2, Ar, O2, and CO measured by the MSL Curiosity quadrupole mass spectrometer must be corrected for the seasonal variations of the atmospheric pressure to reproduce annual mean mixing ratios on Mars. The corrections are made using measurements the Viking Landers and the Mars Climate Database data. The mean correction factor is 0.899 ± 0.006 resulting in annual mean mixing ratios of (1.83 ± 0.03)% for N2, (1.86 ± 0.02)% for Ar, (1.56 ± 0.06)×10-3 for O2, and 673 ± 2.6 ppm for CO. The O2 mixing ratio agrees with the Herschel value within its uncertainty, the ground-based observations corrected for the dust extinction, and photochemical models by Nair et al. (1994) and Krasnopolsky (2010). The CO mixing ratio is in excellent agreement with the MRO/CRISM value of 700 ppm and with 667, 693, and 684 ppm recently observed at LS = 60, 89, and 110° and corrected to the annual mean conditions. Lifetimes of N2 and Ar are very long in the martian atmosphere, and differences between the MSL and Viking data on these species cannot be attributed to their variations.

  15. Simple model to estimate the contribution of atmospheric CO2 to the Earth's greenhouse effect

    NASA Astrophysics Data System (ADS)

    Wilson, Derrek J.; Gea-Banacloche, Julio

    2012-04-01

    We show how the CO2 contribution to the Earth's greenhouse effect can be estimated from relatively simple physical considerations and readily available spectroscopic data. In particular, we present a calculation of the "climate sensitivity" (that is, the increase in temperature caused by a doubling of the concentration of CO2) in the absence of feedbacks. Our treatment highlights the important role played by the frequency dependence of the CO2 absorption spectrum. For pedagogical purposes, we provide two simple models to visualize different ways in which the atmosphere might return infrared radiation back to the Earth. The more physically realistic model, based on the Schwarzschild radiative transfer equations, uses as input an approximate form of the atmosphere's temperature profile, and thus includes implicitly the effect of heat transfer mechanisms other than radiation.

  16. Trends in land surface phenology and atmospheric CO2 seasonality in the Northern Hemisphere terrestrial ecosystems

    NASA Astrophysics Data System (ADS)

    Gonsamo, A.; Chen, J. M.

    2017-12-01

    Northern terrestrial ecosystems have shown global warming-induced advances in start, delays in end, and thus increased lengths of growing season and gross photosynthesis in recent decades. The tradeoffs between seasonal dynamics of two opposing fluxes, CO2 uptake through photosynthesis and release through respiration, determine the influence of the terrestrial ecosystems on the atmospheric CO2 concentration and 13C/12C isotope ratio seasonality. Atmospheric CO2 and 13C/12C seasonality is controlled by vegetation phenology, but is not identical because growth will typically commence some time before and terminate some time after the net carbon exchange changes sign in spring and autumn, respectively. Here, we use 34-year satellite normalized difference vegetation index (NDVI) observations to determine how changes in vegetation productivity and phenology affect both the atmospheric CO2 and 13C/12C seasonality. Differences and similarities in recent trends of CO2 and 13C/12C seasonality and vegetation phenology will be discussed. Furthermore, we use the NDVI observations, and atmospheric CO2 and 13C/12C data to show the trends and variability of the timing of peak season plant activity. Preliminary results show that the peak season plant activity of the Northern Hemisphere extra-tropical terrestrial ecosystems is shifting towards spring, largely in response to the warming-induced advance of the start of growing season. Besides, the spring-ward shift of the peak plant activity is contributing the most to the increasing peak season productivity. In other words, earlier start of growing season is highly linked to earlier arrival of peak of season and higher NDVI. Changes in the timing of peak season plant activity are expected to disrupt the synchrony of biotic interaction and exert strong biophysical feedbacks on climate by modifying the surface albedo and energy budget.

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

    NASA Astrophysics Data System (ADS)

    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

  18. Porous Ionic Polymers as a Robust and Efficient Platform for Capture and Chemical Fixation of Atmospheric CO2.

    PubMed

    Sun, Qi; Jin, Yingyin; Aguila, Briana; Meng, Xiangju; Ma, Shengqian; Xiao, Feng-Shou

    2017-03-22

    Direct use of atmospheric CO 2 as a C 1 source to synthesize high-value chemicals through environmentally benign processes is of great interest, yet challenging. Porous heterogeneous catalysts that are capable of simultaneously capturing and converting CO 2 are promising candidates for such applications. Herein, a family of organic ionic polymers with nanoporous structure, large surface area, strong affinity for CO 2 , and very high density of catalytic active sites (halide ions) was synthesized through the free-radical polymerization of vinylfunctionalized quaternary phosphonium salts. The resultant porous ionic polymers (PIPs) exhibit excellent activities in the cycloaddition of epoxides with atmospheric CO 2 , outperforming the corresponding soluble phosphonium salt analogues and ranking among the highest of known metal-free catalytic systems. The high CO 2 uptake capacity of the PIPs facilitates the enrichment of CO 2 molecules around the catalytic centers, thereby benefiting its conversion. We have demonstrated for the first time that atmospheric CO 2 can be directly converted to cyclic carbonates at room temperature using a heterogeneous catalytic system under metal-solvent free conditions. Moreover, the catalysts proved to be robust and fully recyclable, demonstrating promising potential for practical utilization for the chemical fixation of CO 2 . Our work thereby paves a way to the advance of PIPs as a new type of platform for capture and conversion of CO 2 . © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  19. Carbon assimilation in Eucalyptus urophylla grown under high atmospheric CO2 concentrations: A proteomics perspective.

    PubMed

    Santos, Bruna Marques Dos; Balbuena, Tiago Santana

    2017-01-06

    Photosynthetic organisms may be drastically affected by the future climate projections of a considerable increase in CO 2 concentrations. Growth under a high concentration of CO 2 could stimulate carbon assimilation-especially in C3-type plants. We used a proteomics approach to test the hypothesis of an increase in the abundance of the enzymes involved in carbon assimilation in Eucalyptus urophylla plants grown under conditions of high atmospheric CO 2 . Our strategy allowed the profiling of all Calvin-Benson cycle enzymes and associated protein species. Among the 816 isolated proteins, those involved in carbon fixation were found to be the most abundant ones. An increase in the abundance of six key enzymes out of the eleven core enzymes involved in carbon fixation was detected in plants grown at a high CO 2 concentration. Proteome changes were corroborated by the detection of a decrease in the stomatal aperture and in the vascular bundle area in Eucalyptus urophylla plantlets grown in an environment of high atmospheric CO 2 . Our proteomics approach indicates a positive metabolic response regarding carbon fixation in a CO 2 -enriched atmosphere. The slight but significant increase in the abundance of the Calvin enzymes suggests that stomatal closure did not prevent an increase in the carbon assimilation rates. The sample enrichment strategy and data analysis used here enabled the identification of all enzymes and most protein isoforms involved in the Calvin-Benson-Bessham cycle in Eucalyptus urophylla. Upon growth in CO 2 -enriched chambers, Eucalyptus urophylla plantlets responded by reducing the vascular bundle area and stomatal aperture size and by increasing the abundance of six of the eleven core enzymes involved in carbon fixation. Our proteome approach provides an estimate on how a commercially important C3-type plant would respond to an increase in CO 2 concentrations. Additionally, confirmation at the protein level of the predicted genes involved in

  20. A review of elevated atmospheric CO2 effects on plant growth and water relations: implications for horticulture

    USDA-ARS?s Scientific Manuscript database

    Empirical records provide incontestable evidence for the global rise in CO2 concentration in the earth's atmosphere. Plant growth can be stimulated by elevation of CO2; photosynthesis increases and economic yield is often enhanced. The application of more CO2 can increase plant water use efficiency ...

  1. Combined effects of deforestation and doubled atmospheric CO{sub 2} concentrations on the climate of Amazonia

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Costa, M.H.; Foley, J.A.

    2000-01-01

    It is generally expected that the Amazon basin will experience at least two major environmental changes during the next few decades and centuries: (1) increasing areas of forest will be converted to pasture and cropland, and (2) concentrations of atmospheric CO{sub 2} will continue to rise. In this study, the authors use the National Center for Atmospheric Research GENESIS atmospheric general circulation model, coupled to the Integrated Biosphere Simulator, to determine the combined effects of large-scale deforestation and increased CO{sub 2} concentrations (including both physiological and radiative effects) on Amazonian climate. In these simulations, deforestation decreases basin-average precipitation by 0.73more » mm day{sup {minus}1} over the basin, as a consequence of the general reduction in vertical motion above the deforested area (although there are some small regions with increased vertical motion). The overall effect of doubled CO{sub 2} concentrations in Amazonia is an increase in basin-average precipitation of 0.28 mm day{sup {minus}1}. The combined effect of deforestation and doubled CO{sub 2}, including the interactions among the processes, is a decrease in the basin-average precipitation of 0.42 mm day{sup {minus}1}. While the effects of deforestation and increasing CO{sub 2} concentrations on precipitation tend to counteract one another, both processes work to warm the Amazon basin. The effect of deforestation and increasing CO{sub 2} concentrations both tent to increase surface temperature, mainly because of decreases in evapotranspiration and the radiative effect of CO{sub 2}. The combined effect of deforestation and doubled CO{sub 2}, including the interactions among the processes, increases the basin-average temperature by roughly 3.5 C.« less

  2. Impacts of elevated atmospheric CO2 and O3 on Paper Birch (Betula papyrifera): reproductive fitness

    Treesearch

    Joseph N.T. Darbah; Mark E. Kubiske; Neil Nelson; Elina Oksanen; Elina Vaapavuori; David F. Karnosky

    2007-01-01

    Atmospheric CO2 and tropospheric O3 are rising in many regions of the world. Little is known about how these two commonly co-occurring gases will affect reproductive fitness of important forest tree species. Here, we report on the long-term effects of CO2 and O3 for paper birch...

  3. Characteristics of CO2 release from forest soil in the mountains near Beijing.

    PubMed

    Sun, Xiang Yang; Gao, Cheng Da; Zhang, Lin; Li, Su Yan; Qiao, Yong

    2011-04-01

    CO2 release from forest soil is a key driver of carbon cycling between the soil and atmosphere ecosystem. The rate of CO2 released from soil was measured in three forest stands (in the mountainous region near Beijing, China) by the alkaline absorption method from 2004 to 2006. The rate of CO2 released did not differ among the three stands. The CO2 release rate ranged from - 341 to 1,193 mg m(-2) h(-1), and the mean value over all three forests and sampling times was 286 mg m(-2) h(-1). CO2 release was positively correlated with soil water content and the soil temperature. Diurnally, CO2 release was higher in the day than at night. Seasonally, CO2 release was highest in early autumn and lowest in winter; in winter, negative values of CO2 release suggested that CO2 was absorbed by soil.

  4. Three-dimensional variations of atmospheric CO2: aircraft measurements and multi-transport model simulations

    NASA Astrophysics Data System (ADS)

    Niwa, Y.; Patra, P. K.; Sawa, Y.; Machida, T.; Matsueda, H.; Belikov, D.; Maki, T.; Ikegami, M.; Imasu, R.; Maksyutov, S.; Oda, T.; Satoh, M.; Takigawa, M.

    2011-12-01

    Numerical simulation and validation of three-dimensional structure of atmospheric carbon dioxide (CO2) is necessary for quantification of transport model uncertainty and its role on surface flux estimation by inverse modeling. Simulations of atmospheric CO2 were performed using four transport models and two sets of surface fluxes compared with an aircraft measurement dataset of Comprehensive Observation Network for Trace gases by AIrLiner (CONTRAIL), covering various latitudes, longitudes, and heights. Under this transport model intercomparison project, spatiotemporal variations of CO2 concentration for 2006-2007 were analyzed with a three-dimensional perspective. Results show that the models reasonably simulated vertical profiles and seasonal variations not only over northern latitude areas but also over the tropics and southern latitudes. From CONTRAIL measurements and model simulations, intrusion of northern CO2 in to the Southern Hemisphere, through the upper troposphere, was confirmed. Furthermore, models well simulated the vertical propagation of seasonal variation in the northern free troposphere. However, significant model-observation discrepancies were found in Asian regions, which are attributable to uncertainty of the surface CO2 flux data. In summer season, differences in latitudinal gradients by the fluxes are comparable to or greater than model-model differences even in the free troposphere. This result suggests that active summer vertical transport sufficiently ventilates flux signals up to the free troposphere and the models could use those for inferring surface CO2 fluxes.

  5. Performance of a new carbon dioxide absorbent, Yabashi lime® as compared to conventional carbon dioxide absorbent during sevoflurane anesthesia in dogs.

    PubMed

    Kondoh, Kei; Atiba, Ayman; Nagase, Kiyoshi; Ogawa, Shizuko; Miwa, Takashi; Katsumata, Teruya; Ueno, Hiroshi; Uzuka, Yuji

    2015-08-01

    In the present study, we compare a new carbon dioxide (CO2) absorbent, Yabashi lime(®) with a conventional CO2 absorbent, Sodasorb(®) as a control CO2 absorbent for Compound A (CA) and Carbon monoxide (CO) productions. Four dogs were anesthetized with sevoflurane. Each dog was anesthetized with four preparations, Yabashi lime(®) with high or low-flow rate of oxygen and control CO2 absorbent with high or low-flow rate. CA and CO concentrations in the anesthetic circuit, canister temperature and carbooxyhemoglobin (COHb) concentration in the blood were measured. Yabashi lime(®) did not produce CA. Control CO2 absorbent generated CA, and its concentration was significantly higher in low-flow rate than a high-flow rate. CO was generated only in low-flow rate groups, but there was no significance between Yabashi lime(®) groups and control CO2 absorbent groups. However, the CO concentration in the circuit could not be detected (≤5ppm), and no change was found in COHb level. Canister temperature was significantly higher in low-flow rate groups than high-flow rate groups. Furthermore, in low-flow rate groups, the lower layer of canister temperature in control CO2 absorbent group was significantly higher than Yabashi lime(®) group. CA and CO productions are thought to be related to the composition of CO2 absorbent, flow rate and canister temperature. Though CO concentration is equal, it might be safer to use Yabashi lime(®) with sevoflurane anesthesia in dogs than conventional CO2 absorbent at the point of CA production.

  6. Retrieving CO2 from Orbiting Carbon Observatory-2 (OCO-2) Spectra

    NASA Astrophysics Data System (ADS)

    Crisp, David

    2014-06-01

    Fossil fuel combustion, deforestation, and other human activities are currently adding almost 40 billion tons of carbon dioxide (CO2) to the atmosphere each year. These emissions have increased by roughly a factor of 3 over the past half century and are still growing by more than 2% per year. The developing world is now responsible for the majority (57%) of these emissions and their rapid growth rates. Precise measurements collected by a global network of surface stations show that these emissions have contributed to a 25% increase in the atmospheric CO2 concentration over the past half century. Surprisingly, comparisons of these measurements with fossil fuel emission inventories indicate that only about half of the CO2 emitted into the atmosphere by human activities stays there. The rest is apparently being absorbed by natural CO2 "sinks" at the Earth's surface. Measurements of the pH of the ocean indicate that it absorbs roughly one quarter of these emissions. The remainder has been attributed to the land biosphere, but the identity and location of the land sinks is still unknown. In addition, the fraction of the anthropogenic CO2 absorbed by these natural sinks has varied dramatically from year to year, but has remained near 1/2 on decadal time scales as the emissions have steadily increased. Uncertainties in the nature, location, and processes controlling these natural sink largely preclude reliable predictions of future atmospheric CO2 buildup rates. The existing greenhouse gas monitoring network can accurately track CO2 changes on hemispheric to global scales, but does not have the resolution or coverage needed to quantify emission sources on regional scales or to identify the natural sinks responsible for absorbing CO2. One way to improve the measurement density is to retrieve precise, spatially-resolved estimates of the column-averaged CO2 dry air mole fraction, XCO2, from satellites. Surface-weighted estimates of XCO2 can be retrieved from measurements of

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

    NASA Astrophysics Data System (ADS)

    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.

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

    NASA Astrophysics Data System (ADS)

    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.

  9. The effects of atmospheric [CO2] on carbon isotope fractionation and magnesium incorporation into biogenic marine calcite

    NASA Technical Reports Server (NTRS)

    Vieira, Veronica

    1997-01-01

    The influences of atmospheric carbon dioxide on the fractionation of carbon isotopes and the magnesium incorporation into biogenic marine calcite were investigated using samples of the calcareous alga Amphiroa and benthic foraminifer Sorites grown in the Biosphere 2 Ocean system under variable atmospheric CO2 concentrations (approximately 500 to 1200 ppm). Carbon isotope fractionation was studied in both the organic matter and the skeletal carbonate. Magnesium analysis was to be performed on the carbonate removed during decalcification. These data have not been collected due to technical problems. Carbon isotope data from Amphiroa yields a linear relation between [CO2] and Delta(sup 13)C(sub Corg)values suggesting that the fractionation of carbon isotopes during photosynthesis is positively correlated with atmospheric [CO2]. [CO2] and Delta(sup 13)C(sub Corg) values for Sorites produce a relation that is best described by a hyperbolic function where Delta(sup 13)C(sub Corg) values increase between 300 and 700 ppm and decrease from 700 to 1200 ppm. Further investigation of this relation and Sorites physiology is needed.

  10. The role of Southern Ocean mixing and upwelling in glacial-interglacial atmospheric CO2 change

    NASA Astrophysics Data System (ADS)

    Watson, Andrew J.; Naveira Garabato, Alberto C.

    2006-02-01

    Decreased ventilation of the Southern Ocean in glacial time is implicated in most explanations of lower glacial atmospheric CO2. Today, the deep (>2000 m) ocean south of the Polar Front is rapidly ventilated from below, with the interaction of deep currents with topography driving high mixing rates well up into the water column. We show from a buoyancy budget that mixing rates are high in all the deep waters of the Southern Ocean. Between the surface and ~2000 m depth, water is upwelled by a residual meridional overturning that is directly linked to buoyancy fluxes through the ocean surface. Combined with the rapid deep mixing, this upwelling serves to return deep water to the surface on a short time scale. We propose two new mechanisms by which, in glacial time, the deep Southern Ocean may have been more isolated from the surface. Firstly, the deep ocean appears to have been more stratified because of denser bottom water resulting from intense sea ice formation near Antarctica. The greater stratification would have slowed the deep mixing. Secondly, subzero atmospheric temperatures may have meant that the present-day buoyancy flux from the atmosphere to the ocean surface was reduced or reversed. This in turn would have reduced or eliminated the upwelling (contrary to a common assumption, upwelling is not solely a function of the wind stress but is coupled to the air-sea buoyancy flux too). The observed very close link between Antarctic temperatures and atmospheric CO2 could then be explained as a natural consequence of the connection between the air-sea buoyancy flux and upwelling in the Southern Ocean, if slower ventilation of the Southern Ocean led to lower atmospheric CO2. Here we use a box model, similar to those of previous authors, to show that weaker mixing and reduced upwelling in the Southern Ocean can explain the low glacial atmospheric CO2 in such a formulation.

  11. [Direct Observation on the Temporal and Spatial Patterns of the CO2 Concentration in the Atmospheric of Nanjing Urban Canyon in Summer].

    PubMed

    Gao, Yun-qiu; Liu, Shou-dong; Hu, Ning; Wang, Shu-min; Deng, Li-chen; Yu, Zhou; Zhang, Zhen; Li, Xu-hui

    2015-07-01

    Direct observation of urban atmospheric CO2 concentration is vital for the research in the contribution of anthropogenic activity to the atmospheric abundance since cities are important CO2 sources. The observations of the atmospheric CO2 concentration at multiple sites/heights can help us learn more about the temporal and spatial patterns and influencing mechanisms. In this study, the CO2 concentration was observed at 5 sites (east, west, south, north and middle) in the main city area of Nanjing from July 18 to 25, 2014, and the vertical profile of atmospheric CO2 concentration was measured in the middle site at 3 heights (30 m, 65 m and 110 m). The results indicated that: (1) An obvious vertical CO2 gradient was found, with higher CO2 concentration [molar fraction of 427. 3 x 10(-6) (±18. 2 x 10(-6))] in the lower layer due to the strong influences of anthropogenic emissions, and lower CO2 concentration in the upper layers [411. 8 x 10(-6) (±15. 0 x 10(-6)) and 410. 9 x 10(-6) (±14. 6 x 10(-6)) at 65 and 110 m respectively] for the well-mixed condition. The CO2 concentration was higher and the vertical gradient was larger when the atmosphere was stable. (2) The spatial distribution pattern of CO2 concentration was dominated by wind and atmospheric stability. During the observation, the CO2 concentration in the southwest was higher than that in the northeast region with the CO2 concentration difference of 7. 8 x 10(-6), because the northwest wind was prevalent. And the CO2 concentration difference reduced with increasing wind speed since stronger wind diluted CO2 more efficiently. The more stable the atmosphere was, the higher the CO2 concentration was. (3) An obvious diurnal variation of CO2 concentration was shown in the 5 sites. A peak value occurred during the morning rush hours, the valley value occurred around 17:00 (Local time) and another high value occurred around 19:00 because of evening rush hour sometimes.

  12. Delta 14CO2 Record from Vermunt, Austria, February 1959 - June 1983

    DOE Data Explorer

    Levin, Ingeborg [Institut fur Umweltphysik, University of Heidelberg, Germany; Kromer, Bernd [Institut fur Umweltphysik, University of Heidelberg, Germany; Schoch-Fischer, H. [Institut fur Umweltphysik, University of Heidelberg, Germany; Bruns, M. [Institut fur Umweltphysik, University of Heidelberg, Germany; Munnich, M. [Institut fur Umweltphysik, University of Heidelberg, Germany; Berdau, D. [Institut fur Umweltphysik, University of Heidelberg, Germany; Vogel, J. C. [Institut fur Umweltphysik, University of Heidelberg, Germany; Munnich, K. O. [Institut fur Umweltphysik, University of Heidelberg, Germany

    1994-01-01

    The sampling at Vermunt was discontinued in 1983. During sampling from 1959 to 1983, the sampling methods were modified twice (Levin et al. 1985). From 1959 through November 1965, three dishes with 1.5 L of 0.5 normal sodium hydroxide (NaOH) carbonate-free solution were exposed to the atmosphere for ~3 days, and the atmospheric CO2 absorbed during that time was recovered by acid evolution. From November 1965 through May 1975, samples were collected by pumping fresh air continuously for 10 days through a box containing 1.5 L of a 0.5 normal NaOH solution. The method has been described by Münnich and Vogel (1959). From May 1975 to the time sampling stopped, a technique described by Levin et al. (1980) was used. Air was pumped through a rotating glass tube filled with a packed bed of Raschig rings (hard glass) to enlarge the surface of the absorbing NaOH solution (200 ml of 4 normal NaOH). The CO2 absorption was quantitative and samples represent mean values of 10 days to 2 weeks. In the laboratory, the samples were extracted from the NaOH solution in a vacuum system by adding hydrochloric or sulfuric acid. The CO2 gas samples were purified over charcoal and counted in a proportional counter (Schoch et al. 1980). Delta 14C values are given relative to the NIST oxalic acid activity corrected for decay (Stuiver and Polach 1970).

  13. An approach for verifying biogenic greenhouse gas emissions inventories with atmospheric CO 2 concentration data

    DOE PAGES

    Ogle, Stephen; Davis, Kenneth J.; Lauvaux, Thomas; ...

    2015-03-10

    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. Verification could include a variety of evidence, but arguably the most convincing verification would be confirmation of a change in GHG concentrations in the atmosphere that is consistent with reported emissions to the UNFCCC. We report here on a case study evaluating this option based on a prototype atmospheric CO2 measurement network deployed in the Mid-Continent Region of themore » conterminous United States. We found that the atmospheric CO2 measurement data did verify the accuracy of the emissions inventory within the confidence limits of the emissions estimates, suggesting that this technology could be further developed and deployed more widely in the future for verifying reported emissions.« less

  14. Impacts of 3 years of elevated atmospheric CO2 on rhizosphere carbon flow and microbial community dynamics.

    PubMed

    Drigo, Barbara; Kowalchuk, George A; Knapp, Brigitte A; Pijl, Agata S; Boschker, Henricus T S; van Veen, Johannes A

    2013-02-01

    Carbon (C) uptake by terrestrial ecosystems represents an important option for partially mitigating anthropogenic CO2 emissions. Short-term atmospheric elevated CO2 exposure has been shown to create major shifts in C flow routes and diversity of the active soil-borne microbial community. Long-term increases in CO2 have been hypothesized to have subtle effects due to the potential adaptation of soil microorganism to the increased flow of organic C. Here, we studied the effects of prolonged elevated atmospheric CO2 exposure on microbial C flow and microbial communities in the rhizosphere. Carex arenaria (a nonmycorrhizal plant species) and Festuca rubra (a mycorrhizal plant species) were grown at defined atmospheric conditions differing in CO2 concentration (350 and 700 ppm) for 3 years. During this period, C flow was assessed repeatedly (after 6 months, 1, 2, and 3 years) by (13) C pulse-chase experiments, and label was tracked through the rhizosphere bacterial, general fungal, and arbuscular mycorrhizal fungal (AMF) communities. Fatty acid biomarker analyses and RNA-stable isotope probing (RNA-SIP), in combination with real-time PCR and PCR-DGGE, were used to examine microbial community dynamics and abundance. Throughout the experiment the influence of elevated CO2 was highly plant dependent, with the mycorrhizal plant exerting a greater influence on both bacterial and fungal communities. Biomarker data confirmed that rhizodeposited C was first processed by AMF and subsequently transferred to bacterial and fungal communities in the rhizosphere soil. Over the course of 3 years, elevated CO2 caused a continuous increase in the (13) C enrichment retained in AMF and an increasing delay in the transfer of C to the bacterial community. These results show that, not only do elevated atmospheric CO2 conditions induce changes in rhizosphere C flow and dynamics but also continue to develop over multiple seasons, thereby affecting terrestrial ecosystems C utilization processes

  15. Pressure Sounding of the Middle Atmosphere from ATMOS Solar Occultation Measurements of Atmospheric CO(sub 2) Absorption Lines

    NASA Technical Reports Server (NTRS)

    Abrams, M.; Gunson, M.; Lowes, L.; Rinsland, C.; Zander, R.

    1994-01-01

    A method for retrieving the atmospheric pressure corresponding to the tangent point of an infrared spectrum recorded in the solar occultation mode is described and applied to measurements made by the Atmospheric Trace Molecule Spectroscopy (ATMOS) Fourier transform spectrometer. Tangent pressure values are inferred from measurements of isolated CO(sub 2) lines with temperature-insensitive intensities. Tangent pressures are determined with a spectroscopic precision of 1-3%, corresponding to a tangent point height precision, depending on the scale height, of 70-210 meters.

  16. Comment on "Scrutinizing the carbon cycle and CO2residence time in the atmosphere" by H. Harde

    NASA Astrophysics Data System (ADS)

    Köhler, Peter; Hauck, Judith; Völker, Christoph; Wolf-Gladrow, Dieter A.; Butzin, Martin; Halpern, Joshua B.; Rice, Ken; Zeebe, Richard E.

    2018-05-01

    Harde (2017) proposes an alternative accounting scheme for the modern carbon cycle and concludes that only 4.3% of today's atmospheric CO2 is a result of anthropogenic emissions. As we will show, this alternative scheme is too simple, is based on invalid assumptions, and does not address many of the key processes involved in the global carbon cycle that are important on the timescale of interest. Harde (2017) therefore reaches an incorrect conclusion about the role of anthropogenic CO2 emissions. Harde (2017) tries to explain changes in atmospheric CO2 concentration with a single equation, while the most simple model of the carbon cycle must at minimum contain equations of at least two reservoirs (the atmosphere and the surface ocean), which are solved simultaneously. A single equation is fundamentally at odds with basic theory and observations. In the following we will (i) clarify the difference between CO2 atmospheric residence time and adjustment time, (ii) present recently published information about anthropogenic carbon, (iii) present details about the processes that are missing in Harde (2017), (iv) briefly discuss shortcoming in Harde's generalization to paleo timescales, (v) and comment on deficiencies in some of the literature cited in Harde (2017).

  17. A multiscale and multidisciplinary investigation of ecosystem-atmosphere CO2 exchange over the rocky mountains of colorado

    USGS Publications Warehouse

    Sun, Jielun; Oncley, S.P.; Burns, Sean P.; Stephens, B.B.; Lenschow, D.H.; Campos, T.; Monson, Russell K.; Schimel, D.S.; Sacks, W.J.; De Wekker, S. F. J.; Lai, C.-T.; Lamb, B.; Ojima, D.; Ellsworth, P.Z.; Sternberg, L.S.L.; Zhong, S.; Clements, C.; Moore, D.J.P.; Anderson, D.E.; Watt, A.S.; Hu, Jiawen; Tschudi, M.; Aulenbach, S.; Allwine, E.; Coons, T.

    2010-01-01

    A field study combined with modeling investigation demonstrated that the organization of CO2 transport by mountain terrain strongly affects the regional CO2 budget. Atmospheric dynamics can lead to complicated flows generated by inhomogeneous landscapes, topography or synoptic weather systems. The field campaign conducted of a ground deployment, the Carbon in the Mountain Experiment (CME04), and an aircraft deployment of the national Center for Atmospheric Research (NCAR) C-130, the Airborne Carbon in the Mountains Experiment (ACME04) over the period of spring to fall of 2004 to cover the seasonal variation of ecosystem-atmosphere carbon exchange. The role of the mountain circulation in CO2 transport can be played over seemingly flat terrain by mesoscale flows generated by various physical processes. The three dimensional observation strategy considered can also be applied over flat terrain.

  18. [Effect of elevated atmospheric CO2 on soil urease and phosphatase activities].

    PubMed

    Chen, Lijun; Wu, Zhijie; Huang, Guohong; Zhou, Likai

    2002-10-01

    The response of soil urease and phosphatase activities at different rice growth stages to free air CO2 enrichment (FACE) was studied. The results showed that comparing with the ambient atmospheric CO2 concentration (370 mumol.mol-1), FACE (570 mumol.mol-1) significantly increased the urease activity of 0-5 cm soil layer at the vigorous growth stage of rice, whole that of 5-10 cm layer had no significant change during the whole growing season. Phosphatase activity of 0-5 cm and 5-10 cm soil layers significantly increased, and the peak increment was at the vigorous growth stage of rice.

  19. Venus Upper Clouds and the UV Absorber From MESSENGER/MASCS Observations

    NASA Astrophysics Data System (ADS)

    Pérez-Hoyos, S.; Sánchez-Lavega, A.; García-Muñoz, A.; Irwin, P. G. J.; Peralta, J.; Holsclaw, G.; McClintock, W. M.; Sanz-Requena, J. F.

    2018-01-01

    One of the most intriguing, long-standing questions regarding Venus's atmosphere is the origin and distribution of the unknown UV absorber, responsible for the absorption band detected at the near-UV and blue range of Venus's spectrum. In this work, we use data collected by Mercury Atmospheric and Surface Composition Spectrometer (MASCS) spectrograph on board the MErcury Surface, Space ENvironment, GEochemistry, and Ranging (MESSENGER) mission during its second Venus flyby in June 2007 to address this issue. Spectra range from 0.3 μm to 1.5 μm including some gaseous H2O and CO2 bands, as well as part of the SO2 absorption band and the core of the UV absorption. We used the NEMESIS radiative transfer code and retrieval suite to investigate the vertical distribution of particles in the equatorial atmosphere and to retrieve the imaginary refractive indices of the UV absorber, assumed to be well mixed with Venus's small mode 1 particles. The results show a homogeneous equatorial atmosphere, with cloud tops (height for unity optical depth) at 75 ± 2 km above surface. The UV absorption is found to be centered at 0.34 ± 0.03 μm with a full width at half maximum of 0.14 ± 0.01 μm. Our values are compared with previous candidates for the UV aerosol absorber, among which disulfur oxide (S2O) and dioxide disulfur (S2O2) provide the best agreement with our results.

  20. Regional contributions of ocean iron fertilization to atmospheric CO2 changes during the last glacial termination

    NASA Astrophysics Data System (ADS)

    Opazo, N. E.; Lambert, F.

    2017-12-01

    Mineral dust aerosols affect climate directly by changing the radiative balance of the Earth, and indirectly by acting as cloud condensation nuclei and by affecting biogeochemical cycles. The impact on marine biogeochemical cycles is primarily through the supply of micronutrients such as iron to nutrient-limited regions of the oceans. Iron fertilization of High Nutrient Low Chlorophyll (HNLC) regions of the oceans is thought to have significantly affected the carbon cycle on glacial-interglacial scales and contributed about one fourth of the 80-100 ppm lowering of glacial atmospheric CO2 concentrations.In this study, we quantify the effect of global dust fluxes on atmospheric CO2 using the cGENIE model, an Earth System Model of Intermediate Complexity with emphasis on the carbon cycle. Global Holocene and Last Glacial Maximum (LGM) dust flux fields were obtained from both dust model simulations and reconstructions based on observational data. The analysis was performed in two stages. In the first instance, we produced 8 global intermediate dust flux fields between Holocene and LGM and simulated the atmospheric CO2 drawdown due to these 10 dust levels. In the second stage, we only changed dust flux levels in specific HNLC regions to isolate the effect of these ocean basins. We thus quantify the contribution of the South Atlantic, the South Pacific, the North Pacific, and the Central Pacific HNLC regions to the total atmospheric CO2 difference due to iron fertilization of the Earth's oceans.

  1. Co-evolution of atmospheres, life, and climate.

    PubMed

    Grenfell, J Lee; Rauer, Heike; Selsis, Franck; Kaltenegger, Lisa; Beichman, Charles; Danchi, William; Eiroa, Carlos; Fridlund, Malcolm; Henning, Thomas; Herbst, Tom; Lammer, Helmut; Léger, Alain; Liseau, René; Lunine, Jonathan; Paresce, Francesco; Penny, Alan; Quirrenbach, Andreas; Röttgering, Huub; Schneider, Jean; Stam, Daphne; Tinetti, Giovanna; White, Glenn J

    2010-01-01

    After Earth's origin, our host star, the Sun, was shining 20-25% less brightly than today. Without greenhouse-like conditions to warm the atmosphere, our early planet would have been an ice ball, and life may never have evolved. But life did evolve, which indicates that greenhouse gases must have been present on early Earth to warm the planet. Evidence from the geological record indicates an abundance of the greenhouse gas CO(2). CH(4) was probably present as well; and, in this regard, methanogenic bacteria, which belong to a diverse group of anaerobic prokaryotes that ferment CO(2) plus H(2) to CH(4), may have contributed to modification of the early atmosphere. Molecular oxygen was not present, as is indicated by the study of rocks from that era, which contain iron carbonate rather than iron oxide. Multicellular organisms originated as cells within colonies that became increasingly specialized. The development of photosynthesis allowed the Sun's energy to be harvested directly by life-forms. The resultant oxygen accumulated in the atmosphere and formed the ozone layer in the upper atmosphere. Aided by the absorption of harmful UV radiation in the ozone layer, life colonized Earth's surface. Our own planet is a very good example of how life-forms modified the atmosphere over the planets' lifetime. We show that these facts have to be taken into account when we discover and characterize atmospheres of Earth-like exoplanets. If life has originated and evolved on a planet, then it should be expected that a strong co-evolution occurred between life and the atmosphere, the result of which is the planet's climate.

  2. Miniaturized Near Infrared Heterodyne Spectroradiometer for Monitoring CO2, CH4 and CO in the Earth Atmosphere

    NASA Astrophysics Data System (ADS)

    Klimchuk, A., Sr.; Rodin, A.; Nadezhdinskiy, A.; Churbanov, D.; Spiridonov, M.

    2014-12-01

    The paper describes the concept of a compact, lightweight heterodyne NIR spectro-radiometer suitable for atmospheric sounding with solar occultations, and the first measurement of CO2 and CH4 absorption near 1.60mm and 1.65 mm with spectral resolution l/dl ~ 5*107. Highly stabilized DFB laser was used as local oscillator, while single model quartz fiber Y-coupler served as a diplexer. Radiation mixed in the single mode fiber was detected by quadratic detector using p-i-n diode within the bandpass of ~10 MHz. Wavelength coverage of spectral measurement was provided by sweeping local oscillator frequency in the range 1,1 см-1. With the exposure time of 10 min, the absorption spectrum of the atmosphere over Moscow has been recorded with S/N ~ 300. We retrieved methane vertical profile using Tikhonov method of smooth functional, which takes into account a priori information about first guess profile. The reference to model methane profile means that the regularization procedure always selects a priorivalues unless the measurements contradict this assumption.The retrieved methane profile demonstrates higher abundances in the lower scale height compared to the assumed model profile, well expected in the megalopolis center. The retrievals sensitivity is limited by 10 ppb, with the exception of the lower part of the profile where the tendency to lower values is revealed. Thus the methane abundance variations may be evaluated with relative accuracy better than 1%, which fits the requirements of greenhouse gas monitoring. The retrievals sensitivity of CO2 is about 1-2 ppm. CO2 observations was also used to estimate stratoshere wind by doppler shift of absorption line. Due to higher spectral resolution, lower sensitivity to atmospheric temperatures and other external factors, compared to heterodyne measurements in the thermal IR spectral range, the described technique provides accuracy comparable with much more complicated high resolution measurements now used in TCCON

  3. Catalytic and atmospheric effects on microwave pyrolysis of corn stover.

    PubMed

    Huang, Yu-Fong; Kuan, Wen-Hui; Chang, Chi-Cheng; Tzou, Yu-Min

    2013-03-01

    Corn stover, which is one of the most abundant agricultural residues around the world, could be converted into valuable biofuels and bio based products by means of microwave pyrolysis. After the reaction at the microwave power level of 500W for the processing time of 30min, the reaction performance under N2 atmosphere was generally better than under CO2 atmosphere. This may be due to the better heat absorbability of CO2 molecules to reduce the heat for stover pyrolysis. Most of the metal-oxide catalysts effectively increased the maximum temperature and mass reduction ratio but lowered the calorific values of solid residues. The gas most produced was CO under N2 atmosphere but CO2 under CO2 atmosphere. Catalyst addition lowered the formation of PAHs and thus made liquid products less toxic. More liquid products and less gas products were generated when using the catalysts possibly due to the existence of the Fischer-Tropsch synthesis. Copyright © 2013 Elsevier Ltd. All rights reserved.

  4. Intermediate time scale response of atmospheric CO 2 following prescribed fire in a longleaf pine forest

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Viner, Brian; Parker, M.; Maze, G.

    Fire plays an essential role in maintaining the structure and function of longleaf pine ecosystems. While the effects of fire on carbon cycle have been measured in previous studies for short periods during a burn and for multiyear periods following the burn, information on how carbon cycle is influenced by such changes over the span of a few weeks to months has yet to be quantified. We have analyzed high-frequency measurements of CO 2 concentration and flux, as well as associated micrometeorological variables, at three levels of the tall Aiken AmeriFlux tower during and after a prescribed burn. Measurements ofmore » the CO 2 concentration and vertical fluxes were examined as well as calculated net ecosystem exchange (NEE) for periods prior to and after the burn. Large spikes in both CO 2 concentration and CO 2 flux during the fire and increases in atmospheric CO 2 concentration and reduced CO 2 flux were observed for several weeks following the burn, particularly below the forest canopy. Both CO 2 measurements and NEE were found to return to their preburn states within 60–90 days following the burn when no statistical significance was found between preburn and postburn NEE. Furthermore, this study examines the micrometeorological conditions during a low-intensity prescribed burn and its short-term effects on local CO 2 dynamics in a forested environment by identifying observable impacts on local measurements of atmospheric CO 2 concentration and fluxes.« less

  5. Intermediate time scale response of atmospheric CO2 following prescribed fire in a longleaf pine forest

    NASA Astrophysics Data System (ADS)

    Viner, B.; Parker, M.; Maze, G.; Varnedoe, P.; Leclerc, M.; Starr, G.; Aubrey, D.; Zhang, G.; Duarte, H.

    2016-10-01

    Fire plays an essential role in maintaining the structure and function of longleaf pine ecosystems. While the effects of fire on carbon cycle have been measured in previous studies for short periods during a burn and for multiyear periods following the burn, information on how carbon cycle is influenced by such changes over the span of a few weeks to months has yet to be quantified. We have analyzed high-frequency measurements of CO2 concentration and flux, as well as associated micrometeorological variables, at three levels of the tall Aiken AmeriFlux tower during and after a prescribed burn. Measurements of the CO2 concentration and vertical fluxes were examined as well as calculated net ecosystem exchange (NEE) for periods prior to and after the burn. Large spikes in both CO2 concentration and CO2 flux during the fire and increases in atmospheric CO2 concentration and reduced CO2 flux were observed for several weeks following the burn, particularly below the forest canopy. Both CO2 measurements and NEE were found to return to their preburn states within 60-90 days following the burn when no statistical significance was found between preburn and postburn NEE. This study examines the micrometeorological conditions during a low-intensity prescribed burn and its short-term effects on local CO2 dynamics in a forested environment by identifying observable impacts on local measurements of atmospheric CO2 concentration and fluxes.

  6. Intermediate time scale response of atmospheric CO 2 following prescribed fire in a longleaf pine forest

    DOE PAGES

    Viner, Brian; Parker, M.; Maze, G.; ...

    2016-10-12

    Fire plays an essential role in maintaining the structure and function of longleaf pine ecosystems. While the effects of fire on carbon cycle have been measured in previous studies for short periods during a burn and for multiyear periods following the burn, information on how carbon cycle is influenced by such changes over the span of a few weeks to months has yet to be quantified. We have analyzed high-frequency measurements of CO 2 concentration and flux, as well as associated micrometeorological variables, at three levels of the tall Aiken AmeriFlux tower during and after a prescribed burn. Measurements ofmore » the CO 2 concentration and vertical fluxes were examined as well as calculated net ecosystem exchange (NEE) for periods prior to and after the burn. Large spikes in both CO 2 concentration and CO 2 flux during the fire and increases in atmospheric CO 2 concentration and reduced CO 2 flux were observed for several weeks following the burn, particularly below the forest canopy. Both CO 2 measurements and NEE were found to return to their preburn states within 60–90 days following the burn when no statistical significance was found between preburn and postburn NEE. Furthermore, this study examines the micrometeorological conditions during a low-intensity prescribed burn and its short-term effects on local CO 2 dynamics in a forested environment by identifying observable impacts on local measurements of atmospheric CO 2 concentration and fluxes.« less

  7. White Mars: A New Model for Mars' Surface and Atmosphere Based on CO 2

    NASA Astrophysics Data System (ADS)

    Hoffman, Nick

    2000-08-01

    A new model is presented for the Amazonian outburst floods on Mars. Rather than the working fluid being water, with the associated difficulties in achieving warm and wet conditions on Mars and on collecting and removing the water before and after the floods, instead this model suggests that CO 2 is the active agent in the "floods." The flow is not a conventional liquid flood but is instead a gas-supported density flow akin to terrestrial volcanic pyroclastic flows and surges and at cryogenic temperatures with support from degassing of CO 2-bearing ices. The flows are not sourced from volcanic vents, but from the collapse of thick layered regolith containing liquid CO 2 to form zones of chaotic terrain, as shown by R. St. J. Lambert and V. E. Chamberlain (1978, Icarus34, 568-580; 1992, Workshop on the Evolution of the Martian Atmosphere). Submarine turbidites are also analagous in the flow mechanism, but the martian cryogenic flows were both dry and subaerial, so there is no need for a warm and wet epoch nor an ocean on Mars. Armed with this new model for the floods we review the activity of volatiles on the surface of Mars in the context of a cold ice world—"White Mars." We find that many of the recognized paradoxes about Mars' surface and atmosphere are resolved. In particular, the lack of carbonates on Mars is due to the lack of liquid water. The CO 2 of the primordial atmosphere and the H 2O inventory remain largely sequestered in subsurface ices. The distribution of water ice on modern Mars is also reevaluated, with important potential consequences for future Mars exploration. The model for collapse of terrain due to ices that show decompression melting, and the generation of nonaqueous flows in these circumstances may also be applicable to outer Solar System bodies, where CO 2, SO 2, N 2, and other ices are stable.

  8. Observational constraint on Pluto's atmospheric CO with ASTE

    NASA Astrophysics Data System (ADS)

    Iino, Takahiro; Hirahara, Yasuhiro; Hidemori, Takehiro; Tsukagoshi, Takashi; Nakajima, Taku; Nakamoto, Satoru; Kato, Chihaya

    2016-02-01

    To confirm the previous observational results of Pluto's atmospheric CO in the J = 2-1 rotational transition, we conducted a new observation of CO (J = 3-2) in Pluto's atmosphere in 2014 August with the Atacama Submillimeter Telescope Experiment 10 m single-dish telescope. In contrast to the previous observational result obtained with the James Clerk Maxwell Telescope in 2009 and 2010 by using the J = 2-1 transition, no emission structure was observed near the rest frequency in our attempt. Possible explanations for the nondetection result of the J = 3-2 transition are discussed.

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

    NASA Astrophysics Data System (ADS)

    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.

  10. Compiled records of carbon isotopes in atmospheric CO2 for historical simulations in CMIP6

    NASA Astrophysics Data System (ADS)

    Graven, Heather; Allison, Colin E.; Etheridge, David M.; Hammer, Samuel; Keeling, Ralph F.; Levin, Ingeborg; Meijer, Harro A. J.; Rubino, Mauro; Tans, Pieter P.; Trudinger, Cathy M.; Vaughn, Bruce H.; White, James W. C.

    2017-12-01

    The isotopic composition of carbon (Δ14C and δ13C) in atmospheric CO2 and in oceanic and terrestrial carbon reservoirs is influenced by anthropogenic emissions and by natural carbon exchanges, which can respond to and drive changes in climate. Simulations of 14C and 13C in the ocean and terrestrial components of Earth system models (ESMs) present opportunities for model evaluation and for investigation of carbon cycling, including anthropogenic CO2 emissions and uptake. The use of carbon isotopes in novel evaluation of the ESMs' component ocean and terrestrial biosphere models and in new analyses of historical changes may improve predictions of future changes in the carbon cycle and climate system. We compile existing data to produce records of Δ14C and δ13C in atmospheric CO2 for the historical period 1850-2015. The primary motivation for this compilation is to provide the atmospheric boundary condition for historical simulations in the Coupled Model Intercomparison Project 6 (CMIP6) for models simulating carbon isotopes in the ocean or terrestrial biosphere. The data may also be useful for other carbon cycle modelling activities.

  11. Carbon Absorber Retrofit Equipment (CARE)

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Klein, Eric

    During Project DE-FE0007528, CARE (Carbon Absorber Retrofit Equipment), Neumann Systems Group (NSG) designed, installed and tested a 0.5MW NeuStream® carbon dioxide (CO 2) capture system using the patented NeuStream® absorber equipment and concentrated (6 molal) piperazine (PZ) as the solvent at Colorado Springs Utilities’ (CSU’s) Martin Drake pulverized coal (PC) power plant. The 36 month project included design, build and test phases. The 0.5MW NeuStream® CO 2 capture system was successfully tested on flue gas from both coal and natural gas combustion sources and was shown to meet project objectives. Ninety percent CO 2 removal was achieved with greater thanmore » 95% CO 2product purity. The absorbers tested support a 90% reduction in absorber volume compared to packed towers and with an absorber parasitic power of less than 1% when configured for operation with a 550MW coal plant. The preliminary techno-economic analysis (TEA) performed by the Energy and Environmental Research Center (EERC) predicted an over-the-fence cost of $25.73/tonne of CO 2 captured from a sub-critical PC plant.« less

  12. Black spruce family growth performance under ambient and elevated atmospheric CO2

    Treesearch

    Kurt H. Johnsen; John E. Major

    1998-01-01

    Abstract. Seedlings from 20 families of black spruce (Picea mariana (Mill.) B.S.P.), representing a large range in field productivity, were subjected to a greenhouse retrospective test under ambient (409 ppm – year 1, 384 ppm – year 2) and high (686 ppm – year 1, 711 ppm – year 2) atmospheric CO2 environments. After one and two...

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

    PubMed

    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.

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

    NASA Astrophysics Data System (ADS)

    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

  15. A High Resolution Late Holocene Paleo-atmospheric Co2 Reconstruction From Stomatal Frequency Analysis of Conifer Needles

    NASA Astrophysics Data System (ADS)

    Kouwenberg, L. L. R.; Kurschner, W. M.; Wagner, F.; Visscher, H.

    An inverse relation of stomatal frequency in leaves of many plant taxa and atmospheric CO2 concentration has been repeatedly demonstrated. Response curves based on this species-specific relation are increasingly used to reconstruct paleo-CO2 levels from stomatal frequency analysis on fossil leaves. This type of atmospheric CO2 records have been produced for a large part of geological history, varying from the Paleozoic to the Holocene. Quaternary glaciochemical records from Antarctica and Greenland suggest that CO2 concentration and temperature are strongly linked, in general CO2 appears to lag temperature change. However, in order to assess this relation, high res- olution records with a precise chronology are needed. During the Holocene, several century-scale climatic fluctuations took place, such as the 8.2 kyr event and the Lit- tle Ice age. Linking these temperature fluctuations to paleo-CO2 concentrations in glaciochemical records can be difficult, because the resolution of ice-cores is gen- erally low and the ice-gas age difference complicates accurate dating. An excellent alternative tool for high-resolution Holocene CO2 reconstructions can be provided by stomatal frequency analysis of leaves from Holocene peat and lake sediments. In this study, it is demonstrated that the western hemlock (Tsuga heterophylla) also ad- justs its stomatal frequency to the historical CO2 rise. After careful proxy-validation, a high resolution paleo-atmospheric CO2 record over the last 2000 years based on subfossil Tsuga heterophylla needles from Mount Rainier (Washington, USA) was re- constructed. Chronology is provided by a suite of AMS carbon isotope dates and the presence of tephra layers from nearby Mt. St Helens. The record reproduces CO2 lev- els around 280 ppmv for the Little Ice Age and the CO2 rise to 365 ppmv over the last 150 years. A prominent feature is a marked rise in CO2 at 350 years AD, gradu- ally declining over the next centuries. The CO2 record will be

  16. 1.6 μm DIAL Measurement and Back Trajectory Analysis of CO2 Concentration Profiles in the Lower-Atmosphere

    NASA Astrophysics Data System (ADS)

    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

  17. Atmospheric CO2 enrichment alters energy assimilation, investment and allocation in Xanthium strumarium.

    PubMed

    Nagel, Jennifer M; Wang, Xianzhong; Lewis, James D; Fung, Howard A; Tissue, David T; Griffin, Kevin L

    2005-05-01

    Energy-use efficiency and energy assimilation, investment and allocation patterns are likely to influence plant growth responses to increasing atmospheric CO2 concentration ([CO2]). Here, we describe the influence of elevated [CO2] on energetic properties as a mechanism of growth responses in Xanthium strumarium. Individuals of X. strumarium were grown at ambient or elevated [CO2] and harvested. Total biomass and energetic construction costs (CC) of leaves, stems, roots and fruits and percentage of total biomass and energy allocated to these components were determined. Photosynthetic energy-use efficiency (PEUE) was calculated as the ratio of total energy gained via photosynthetic activity (Atotal) to leaf CC. Elevated [CO2] increased leaf Atotal, but decreased CC per unit mass of leaves and roots. Consequently, X. strumarium individuals produced more leaf and root biomass at elevated [CO2] without increasing total energy investment in these structures (CCtotal). Whole-plant biomass was associated positively with PEUE. Whole-plant construction required 16.1% less energy than modeled whole-plant energy investment had CC not responded to increased [CO2]. As a physiological mechanism affecting growth, altered energetic properties could positively influence productivity of X. strumarium, and potentially other species, at elevated [CO2].

  18. CO2 Removal and Atmosphere Revitalization Systems for Next Generation Space Flight

    NASA Technical Reports Server (NTRS)

    Luna, Bernadette; Mulloth, Lila M.; Varghese, Mini M.; Hogan, John Andrew

    2010-01-01

    Removal of metabolic CO2 from breathing air is a vital process for life support in all crewed space missions. A CO2 removal processor called the Low Power CO2 Removal (LPCOR) system is being developed in the Bioengineering Branch at NASA Ames Research Center. LPCOR utilizes advanced adsorption and membrane gas separation processes to achieve substantial power and mass reduction when compared to the state-of-the-art carbon dioxide removal assembly (CORA) of the US segment of the International Space Station (ISS). LPCOR is an attractive alternative for use in commercial spacecraft for short-duration missions and can easily be adapted for closed-loop life support applications. NASA envisions a next-generation closed-loop atmosphere revitalization system that integrates advanced CO2 removal, O2 recovery, and trace contaminant control processes to improve overall system efficiency. LPCOR will serve as the front end to such a system. LPCOR is a reliable air revitalization technology that can serve both the near-term and long-term human space flight needs of NASA and its commercial partners.

  19. Effects of increased levels of atmospheric CO2 and high temperatures on rice growth and quality

    PubMed Central

    Waqas, Muhammad Ahmed; Wang, Song-he; Xiong, Xiang-yang; Wan, Yun-fan

    2017-01-01

    The increased atmospheric temperatures resulting from the increased concentration of atmospheric carbon dioxide (CO2) have had a profound influence on global rice production. China serves as an important area for producing and consuming rice. Therefore, exploring the effects of the simultaneously rising levels of atmospheric CO2 and temperatures on rice growth and quality in the future is very important. The present study was designed to measure the most important aspects of variation for rice-related physiological, ecological and quality indices in different growing periods under a simultaneous increase of CO2 and temperature, through simulation experiments in climate-controlled growth chambers, with southern rice as the study object. The results indicated that the ecological indices, rice phenology, and leaf area would decrease under a simultaneous increase of CO2 and temperature. For the physiological indices, Malondialdehyde (MDA) levels increased significantly in the seedling period. However, it showed the trend of increase and subsequent decrease in the heading and filling periods. In addition, the decomposition of soluble protein (SP) and soluble sugar (SS) accelerated in filling period. The rice quality index of the Head Rice Rate showed the decreasing trend and subsequent increase, but the Chalky Rice Rate and Protein Content indices gradually decreased while the Gel Consistency gradually increased. PMID:29145420

  20. Passively Q-switched 1.6 µm Er:YAG laser with a γ-Ga2O3:Co-based glass-ceramics as a saturable absorber

    NASA Astrophysics Data System (ADS)

    Shi, Yang; Gao, Chunqing; Ye, Qing; Wang, Shuo; Wang, Qing; Gao, Mingwei; Loiko, Pavel; Skoptsov, Nikolai; Dymshits, Olga; Zhilin, Alexander; Zapalova, Svetlana; Tsenter, Marina; Vitkin, Vladimir; Mateos, Xavier; Yumashev, Konstantin

    2018-04-01

    A resonantly pumped passively Q-switched Er:YAG laser operating at 1.617 and 1.645 µm is reported with γ-Ga2O3:Co2+-based glass-ceramics (GCs) as a saturable absorber. The maximum average output power achieved from this laser was 273 mW; the highest pulse energy was 5.9 µJ, corresponding to a pulse duration of 3.0 µs at a repetition frequency of 31 kHz. To the best of our knowledge, this is the first time to use the γ-Ga2O3:Co2+-based GC as a passive Q-switcher for Er:YAG lasers and this is also the first time to obtain 1.617 µm and 1.645 µm pulses with a GC-based saturable absorber.

  1. Passive Q-switching of a Tm:YLF laser with a Co2+ doped silver halide saturable absorber

    NASA Astrophysics Data System (ADS)

    Hecht, Harel; Burshtein, Zeev; Katzir, Abraham; Noach, Salman; Sokol, Maxim; Frumker, Eugene; Galun, Ehud; Ishaaya, Amiel A.

    2017-02-01

    We report a successful passive Q-switching of a Tm:YLF laser operating at λ = 1.9 μm, using a Co2+:AgCl0.5Br0.5 saturable absorber. Approximately 200-ns long, 150 μJ pulses were obtained. Increase in pump energy resulted in repetitive pulsing, with a repetition rate approximately proportional to the pump pulse energy. Room-temperature optical transmission saturation curves measured in ∼1-mm thick Co2+:AgCl0.5Br0.5 plates yielded a ground state absorption cross section σgs =(7.8 ± 0.5) ×10-18 cm2 , and an excited state absorption cross section σes =(3.3 ± 0.3) ×10-18 cm2 , at λ = 1.9 μm. The lifetime of the A2(4F) second excited-state of the octahedral O symmetry was τ∗ =(0.6 ± 0.06) ns .

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

    NASA Technical Reports Server (NTRS)

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

    2015-01-01

    This study evaluates the capability of atmospheric CO2 column measurements under cloudy conditions using an airborne intensity-modulated continuous-wave integrated-path-differential-absorption lidar operating in the 1.57-m CO2 absorption band. The atmospheric CO2 column amounts from the aircraft to the tops of optically thick cumulus clouds and to the surface in the presence of optically thin clouds are retrieved from lidar data obtained during the summer 2011 and spring 2013 flight campaigns, respectively.

  3. Atmospheric fossil fuel CO2 traced by 14CO2 and air quality index pollutant observations in Beijing and Xiamen, China.

    PubMed

    Niu, Zhenchuan; Zhou, Weijian; Feng, Xue; Feng, Tian; Wu, Shugang; Cheng, Peng; Lu, Xuefeng; Du, Hua; Xiong, Xiaohu; Fu, Yunchong

    2018-06-01

    Radiocarbon ( 14 C) is the most accurate tracer available for quantifying atmospheric CO 2 derived from fossil fuel (CO 2ff ), but it is expensive and time-consuming to measure. Here, we used common hourly Air Quality Index (AQI) pollutants (AQI, PM 2.5 , PM 10 , and CO) to indirectly trace diurnal CO 2ff variations during certain days at the urban sites in Beijing and Xiamen, China, based on linear relationships between AQI pollutants and CO 2ff traced by 14 C ([Formula: see text]) for semimonthly samples obtained in 2014. We validated these indirectly traced CO 2ff (CO 2ff-in ) concentrations against [Formula: see text] concentrations traced by simultaneous diurnal 14 CO 2 observations. Significant (p < 0.05) strong correlations were observed between each of the separate AQI pollutants and [Formula: see text] for the semimonthly samples. Diurnal variations in CO 2ff traced by each of the AQI pollutants generally showed similar trends to those of [Formula: see text], with high agreement at the sampling site in Beijing and relatively poor agreement at the sampling site in Xiamen. AQI pollutant tracers showed high normalized root-mean-square (NRMS) errors for the summer diurnal samples due to low [Formula: see text] concentrations. After the removal of these summer samples, the NRMS errors for AQI pollutant tracers were in the range of 31.6-64.2%. CO generally showed a high agreement and low NRMS errors among these indirect tracers. Based on these linear relationships, monthly CO 2ff averages at the sampling sites in Beijing and Xiamen were traced using CO concentration as a tracer. The monthly CO 2ff averages at the Beijing site showed a shallow U-type variation. These results indicate that CO can be used to trace CO 2ff variations in Chinese cities with CO 2ff concentrations above 5 ppm.

  4. [Study on the effect of solar spectra on the retrieval of atmospheric CO2 concentration using high resolution absorption spectra].

    PubMed

    Hu, Zhen-Hua; Huang, Teng; Wang, Ying-Ping; Ding, Lei; Zheng, Hai-Yang; Fang, Li

    2011-06-01

    Taking solar source as radiation in the near-infrared high-resolution absorption spectrum is widely used in remote sensing of atmospheric parameters. The present paper will take retrieval of the concentration of CO2 for example, and study the effect of solar spectra resolution. Retrieving concentrations of CO2 by using high resolution absorption spectra, a method which uses the program provided by AER to calculate the solar spectra at the top of atmosphere as radiation and combine with the HRATS (high resolution atmospheric transmission simulation) to simulate retrieving concentration of CO2. Numerical simulation shows that the accuracy of solar spectrum is important to retrieval, especially in the hyper-resolution spectral retrieavl, and the error of retrieval concentration has poor linear relation with the resolution of observation, but there is a tendency that the decrease in the resolution requires low resolution of solar spectrum. In order to retrieve the concentration of CO2 of atmosphere, the authors' should take full advantage of high-resolution solar spectrum at the top of atmosphere.

  5. MAVEN/IUVS Periapse Lyman-alpha Observations: Variability and Constraints on H and CO2 Abundance

    NASA Astrophysics Data System (ADS)

    Hughes, A. C. G.; Chaffin, M.; Mierkiewicz, E. J.; Chaufray, J. Y.; Deighan, J.; Schneider, N. M.; Thiemann, E.; Clarke, J. T.; Mayyasi, M.; Jain, S. K.; Crismani, M. M. J.; Stiepen, A.; Montmessin, F.; Epavier, F.; Stewart, I. F.; McClintock, B.; Holsclaw, G.; Jakosky, B. M.

    2017-12-01

    The abundance of spectroscopic and geomorphologic evidence demonstrating that liquid water once flowed on Mars raises significant questions regarding the history of Martian water and the evolution of the atmosphere into the current hyper-arid climate. Using data from the Imaging UltraViolet Spectrograph (IUVS) onboard the Mars Atmosphere and Volatile EvolutioN (MAVEN) spacecraft, we evaluate the hydrogen Lyman-alpha emission (121.6 nm) across multiple Martian years and solar zenith angles. We create altitude-intensity profiles of atmospheric hydrogen emission using periapse data from all MAVEN orbits to-date. Due to the optically thin emission of the UV-doublet scale height of mid-ultraviolet IUVS data, we are able to indirectly probe the temperature of the atmosphere. By combining mid-ultraviolet and far-ultraviolet IUVS data, we extract temperatures and densities of the upper atmosphere and fit the data using a radiative transfer forward model. Below 120 km, the H Lyman-alpha emission is absorbed by CO2, providing constraint on CO2 in the lower thermosphere. Fitting the altitude-intensity curves below 120 km altitude and comparing spatial and temporal variations of the profiles allows us to constrain CO2 abundances. The results of this work, in combination with other MAVEN findings, will provide better constraints on Martian H and CO2 densities and determining neutral temperatures, as well as a more thorough understanding of the evolution of the Martian atmosphere through time.

  6. Subarctic weathering of mineral wastes provides a sink for atmospheric CO(2).

    PubMed

    Wilson, Siobhan A; Dipple, Gregory M; Power, Ian M; Barker, Shaun L L; Fallon, Stewart J; Southam, Gordon

    2011-09-15

    The mineral waste from some mines has the capacity to trap and store CO(2) within secondary carbonate minerals via the process of silicate weathering. Nesquehonite [MgCO(3)·3H(2)O] forms by weathering of Mg-silicate minerals in kimberlitic mine tailings at the Diavik Diamond Mine, Northwest Territories, Canada. Less abundant Na- and Ca-carbonate minerals precipitate from sewage treatment effluent deposited in the tailings storage facility. Radiocarbon and stable carbon and oxygen isotopes are used to assess the ability of mine tailings to trap and store modern CO(2) within these minerals in the arid, subarctic climate at Diavik. Stable isotopic data cannot always uniquely identify the source of carbon stored within minerals in this setting; however, radiocarbon isotopic data provide a reliable quantitative estimate for sequestration of modern carbon. At least 89% of the carbon trapped within secondary carbonate minerals at Diavik is derived from a modern source, either by direct uptake of atmospheric CO(2) or indirect uptake though the biosphere. Silicate weathering at Diavik is trapping 102-114 g C/m(2)/y within nesquehonite, which corresponds to a 2 orders of magnitude increase over the background rate of CO(2) uptake predicted from arctic and subarctic river catchment data.

  7. Atmospheric CO2 Records from Sites Operated by the Fraunhofer Institute for Atmospheric Environment Research (1978 - 1992)

    DOE Data Explorer

    Sladkovic, R. [Fraunhofer Institute for Atmospheric Environmental Research (IFU), Garmisch-Partenkirchen, Germany; Scheel, H. E. [Fraunhofer Institute for Atmospheric Environmental Research (IFU), Garmisch-Partenkirchen, Germany; Seiler, W. [Fraunhofer Institute for Atmospheric Environmental Research (IFU), Garmisch-Partenkirchen, Germany

    1997-01-01

    The monitoring site at Garmisch-Partenkirchen is considered a grassland valley site. Because of strong local influence (vegetation and meteorology), the CO2 concentrations at Garmisch-Partenkirchen are higher and show greater seasonal amplitudes than the concentrations measured at Wank or Zugspitze. According to the filtered data, the annual atmospheric CO2 concentrations at Garmisch-Partenkirchen increased from 330.2 ppmv in 1978 to 345.1 ppmv in 1986 and from 347.6 ppmv in 1988 to 354.7 ppmv in 1992. The monitoring site at Wank Peak (WMO-BAPMoN station) is located on the grass-covered, rounded top of the mountain, just above the timberline. The mean annual CO2 concentrations at Wank Peak increased from 334.2 ppmv in 1980 to 348.6 ppmv in 1992. The station at Zugspitze is located near the summit of the highest mountain of the German Alps. In 1990, the site of CO2 sampling was changed from a location 250 m below the summit to a new monitoring station (2937 m above MSL) close to the mountain top. Compatibility of the results was seen from measurements conducted in parallel at the two sites for several months. Because of the high elevation of the mountain station, the CO2 measurements at Zugspitze can be considered free of regional contamination most of the time. The mean annual CO2 concentrations at Zugspitze increased from 333.7 ppmv in 1981 to 349.4 ppmv in 1992.

  8. Impact of OH Radical-Initiated H2CO3 Degradation in the Earth's Atmosphere via Proton-Coupled Electron Transfer Mechanism.

    PubMed

    Ghoshal, Sourav; Hazra, Montu K

    2016-02-04

    The decomposition of isolated carbonic acid (H2CO3) molecule into CO2 and H2O (H2CO3 → CO2 + H2O) is prevented by a large activation barrier (>35 kcal/mol). Nevertheless, it is surprising that the detection of the H2CO3 molecule has not been possible yet, and the hunt for the free H2CO3 molecule has become challenging not only in the Earth's atmosphere but also on Mars. In view of this fact, we report here the high levels of quantum chemistry calculations investigating both the energetics and kinetics of the OH radical-initiated H2CO3 degradation reaction to interpret the loss of the H2CO3 molecule in the Earth's atmosphere. It is seen from our study that proton-coupled electron transfer (PCET) and hydrogen atom transfer (HAT) are the two mechanisms by which the OH radical initiates the degradation of the H2CO3 molecule. Moreover, the PCET mechanism is potentially the important one, as the effective barrier, defined as the difference between the zero point vibrational energy (ZPE) corrected energy of the transition state and the total energy of the isolated starting reactants in terms of bimolecular encounters, for the PCET mechanism at the CCSD(T)/6-311++G(3df,3pd) level of theory is ∼3 to 4 kcal/mol lower than the effective barrier height associated with the HAT mechanism. The CCSD(T)/6-311++G(3df,3pd) level predicted effective barrier heights for the degradations of the two most stable conformers of H2CO3 molecule via the PCET mechanism are only ∼2.7 and 4.3 kcal/mol. A comparative reaction rate analysis at the CCSD(T)/6-311++G(3df,3pd) level of theory has also been carried out to explore the potential impact of the OH radical-initiated H2CO3 degradation relative to that from water (H2O), formic acid (FA), acetic acid (AA) and sulfuric acid (SA) assisted H2CO3 → CO2 + H2O decomposition reactions in both the Earth's troposphere and stratosphere. The comparison of the reaction rates reveals that, although the atmospheric concentration of the OH radical is

  9. Improving the Ginkgo CO2 barometer: Implications for the early Cenozoic atmosphere

    NASA Astrophysics Data System (ADS)

    Barclay, Richard S.; Wing, Scott L.

    2016-04-01

    Stomatal properties of fossil Ginkgo have been used widely to infer the atmospheric concentration of CO2 in the geological past (paleo-pCO2). Many of these estimates of paleo-pCO2 have relied on the inverse correlation between pCO2 and stomatal index (SI - the proportion of epidermal cells that are stomata) observed in recent Ginkgo biloba, and therefore depend on the accuracy of this relationship. The SI - pCO2 relationship in G. biloba has not been well documented, however. Here we present new measurements of SI for leaves of G. biloba that grew under pCO2 from 290 to 430 ppm. We prepared and imaged all specimens using a consistent procedure and photo-documented each count. As in prior studies, we found a significant inverse relationship between SI and pCO2, however, the relationship is more linear, has a shallower slope, and a lower correlation coefficient than previously reported. We examined leaves of G. biloba grown under pCO2 of 1500 ppm, but found they had highly variable SI and a large proportion of malformed stomata. We also measured stomatal dimensions, stomatal density, and the carbon isotope composition of G. biloba leaves in order to test a mechanistic model for inferring pCO2. This model overestimated observed pCO2, performing less well than the SI method between 290 and 430 ppm. We used our revised SI-pCO2 response curve, and new observations of selected fossils, to estimate late Cretaceous and Cenozoic pCO2 from fossil Ginkgo adiantoides. All but one of the new estimates is below 800 ppm, and together they show little long-term change in pCO2 or relation to global temperature. The low Paleogene pCO2 levels indicated by the Ginkgo SI proxy are not consistent with the high pCO2 inferred by some climate and carbon cycle models. We cannot currently resolve the discrepancy, but greater agreement between proxy data and models may come from a better understanding of the stomatal response of G. biloba to elevated pCO2, better counts and measurements of

  10. Study on O2 generation and CO2 absorption capability of four co-cultured salad plants in an enclosed system

    NASA Astrophysics Data System (ADS)

    Guo, Shuangsheng; Ai, Weidang; Tang, Yongkang; Cheng, Quanyong; Shen, Yunze; Qin, Lifeng; Ma, Jialu; Zhu, Jingtao; Ren, Jin

    2014-06-01

    The ability to generate O2 and absorb CO2 of several co-cultured vegetable plants in an enclosed system was studied to provide theoretical reference for the future man-plant integrated tests. Four kinds of salad plants (Lactuca sativa L. var. Dasusheng, Lactuca sativa L. var. Youmaicai, Gynura bicolor and Cichorium endivia L.) were grown in the CELSS Integration Test Platform (CITP). The environmental factors including O2 and CO2 concentration were continuously monitored on-line and the plant biomass was measured at the end of the test. The changing rules of O2 and CO2 concentration in the system were basically understood and it was found that the O2 generated by the plants could satisfy the respiratory needs of 1.75 persons by calculation. It was also found that the plants could absorb the CO2 breathed out by 2 persons when the light intensity was raised to 550 mmol m-2 s-1 PPF. The results showed that the co-cultured plants hold good compatibility and excellent O2-generating and CO2-absorbing capability. They could also supply some fresh edible vegetable for a 2-person crew.

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

    NASA Astrophysics Data System (ADS)

    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 ( < 3 %) of the world's land surface 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

  12. Changes in atmospheric CO2 - Influence of the marine biota at high latitude

    NASA Technical Reports Server (NTRS)

    Knox, F.; Mcelroy, M. B.

    1984-01-01

    Approximately half of the nitrogen and phosphorus entering deep waters of the contemporary ocean are transported from the surface in inorganic form as preformed nutrients. A simple model for ocean chemistry is presented and shown to account for the present level of atmospheric CO2. Fluctuations in preformed nutrients, modulated by changes in insolation and circulation at high latitudes, can result in significant variations in CO2. It is suggested that these changes may account for the apparent control on climate exercised by secular variations in the orbital parameters of the earth.

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

    NASA Astrophysics Data System (ADS)

    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

  14. Variations in atmospheric CO2 growth rates coupled with tropical temperature

    PubMed Central

    Wang, Weile; Ciais, Philippe; Nemani, Ramakrishna R.; Canadell, Josep G.; Piao, Shilong; Sitch, Stephen; White, Michael A.; Hashimoto, Hirofumi; Milesi, Cristina; Myneni, Ranga B.

    2013-01-01

    Previous studies have highlighted the occurrence and intensity of El Niño–Southern Oscillation as important drivers of the interannual variability of the atmospheric CO2 growth rate, but the underlying biogeophysical mechanisms governing such connections remain unclear. Here we show a strong and persistent coupling (r2 ≈ 0.50) between interannual variations of the CO2 growth rate and tropical land–surface air temperature during 1959 to 2011, with a 1 °C tropical temperature anomaly leading to a 3.5 ± 0.6 Petagrams of carbon per year (PgC/y) CO2 growth-rate anomaly on average. Analysis of simulation results from Dynamic Global Vegetation Models suggests that this temperature–CO2 coupling is contributed mainly by the additive responses of heterotrophic respiration (Rh) and net primary production (NPP) to temperature variations in tropical ecosystems. However, we find a weaker and less consistent (r2 ≈ 0.25) interannual coupling between CO2 growth rate and tropical land precipitation than diagnosed from the Dynamic Global Vegetation Models, likely resulting from the subtractive responses of tropical Rh and NPP to precipitation anomalies that partly offset each other in the net ecosystem exchange (i.e., net ecosystem exchange ≈ Rh − NPP). Variations in other climate variables (e.g., large-scale cloudiness) and natural disturbances (e.g., volcanic eruptions) may induce transient reductions in the temperature–CO2 coupling, but the relationship is robust during the past 50 y and shows full recovery within a few years after any such major variability event. Therefore, it provides an important diagnostic tool for improved understanding of the contemporary and future global carbon cycle. PMID:23884654

  15. Southern Ocean acidification: a tipping point at 450-ppm atmospheric CO2.

    PubMed

    McNeil, Ben I; Matear, Richard J

    2008-12-02

    Southern Ocean acidification via anthropogenic CO(2) uptake is expected to be detrimental to multiple calcifying plankton species by lowering the concentration of carbonate ion (CO(3)(2-)) to levels where calcium carbonate (both aragonite and calcite) shells begin to dissolve. Natural seasonal variations in carbonate ion concentrations could either hasten or dampen the future onset of this undersaturation of calcium carbonate. We present a large-scale Southern Ocean observational analysis that examines the seasonal magnitude and variability of CO(3)(2-) and pH. Our analysis shows an intense wintertime minimum in CO(3)(2-) south of the Antarctic Polar Front and when combined with anthropogenic CO(2) uptake is likely to induce aragonite undersaturation when atmospheric CO(2) levels reach approximately 450 ppm. Under the IPCC IS92a scenario, Southern Ocean wintertime aragonite undersaturation is projected to occur by the year 2030 and no later than 2038. Some prominent calcifying plankton, in particular the Pteropod species Limacina helicina, have important veliger larval development during winter and will have to experience detrimental carbonate conditions much earlier than previously thought, with possible deleterious flow-on impacts for the wider Southern Ocean marine ecosystem. Our results highlight the critical importance of understanding seasonal carbon dynamics within all calcifying marine ecosystems such as continental shelves and coral reefs, because natural variability may potentially hasten the onset of future ocean acidification.

  16. Reduced net atmospheric CH4 consumption is a sustained response to elevated CO2 in a temperate forest

    USDA-ARS?s Scientific Manuscript database

    We compared nearly continuously from 1998 until 2006 rates of soil atmosphere CH4 exchange at permanently established sampling sites in a temperate loblolly pine (Pinus taeda) forest exposed to ambient (control plots; approx. 380 uL L-1) or elevated (ambient + 200 uL L-1) CO2. Net atmospheric CH4 co...

  17. Water relations and gas exchange in poplar and willow under water stress and elevated atmospheric CO2.

    PubMed

    Johnson, Jon D; Tognetti, Roberto; Paris, Piero

    2002-05-01

    Predictions of shifts in rainfall patterns as atmospheric [CO2] increases could impact the growth of fast growing trees such as Populus spp. and Salix spp. and the interaction between elevated CO2 and water stress in these species is unknown. The objectives of this study were to characterize the responses to elevated CO2 and water stress in these two species, and to determine if elevated CO2 mitigated drought stress effects. Gas exchange, water potential components, whole plant transpiration and growth response to soil drying and recovery were assessed in hybrid poplar (clone 53-246) and willow (Salix sagitta) rooted cuttings growing in either ambient (350 &mgr;mol mol-1) or elevated (700 &mgr;mol mol-1) atmospheric CO2 concentration ([CO2]). Predawn water potential decreased with increasing water stress while midday water potentials remained unchanged (isohydric response). Turgor potentials at both predawn and midday increased in elevated [CO2], indicative of osmotic adjustment. Gas exchange was reduced by water stress while elevated [CO2] increased photosynthetic rates, reduced leaf conductance and nearly doubled instantaneous transpiration efficiency in both species. Dark respiration decreased in elevated [CO2] and water stress reduced Rd in the trees growing in ambient [CO2]. Willow had 56% lower whole plant hydraulic conductivity than poplar, and showed a 14% increase in elevated [CO2] while poplar was unresponsive. The physiological responses exhibited by poplar and willow to elevated [CO2] and water stress, singly, suggest that these species respond like other tree species. The interaction of [CO2] and water stress suggests that elevated [CO2] did mitigate the effects of water stress in willow, but not in poplar.

  18. Effects of Atmospheric and Surface Dust on the Sublimation Rates of CO2 on Mars

    NASA Technical Reports Server (NTRS)

    Bonev, B. P.; James, P. B.; Bjorkman, J. E.; Hansen, G. B.; Wolff, M. J.

    2003-01-01

    We present an overview of our modeling work dedicated to study the effects of atmospheric dust on the sublimation of CO2 on Mars. The purpose of this study is to better understand the extent to which dust storm activity can be a root cause for interannual variability in the planetary CO2 seasonal cycle, through modifying the springtime regression rates of the south polar cap. We obtain calculations of the sublimation fluxes for various types of polar surfaces and different amounts of atmospheric dust. These calculations have been compared qualitatively with the regression patterns observed by Mars Global Surveyor (MGS) in both visible and infrared wavelengths, for two years of very different dust histories (1999, and 2001).

  19. Atmospheric pCO2 reconstructed across five early Eocene global warming events

    NASA Astrophysics Data System (ADS)

    Cui, Ying; Schubert, Brian A.

    2017-11-01

    Multiple short-lived global warming events, known as hyperthermals, occurred during the early Eocene (56-52 Ma). Five of these events - the Paleocene-Eocene Thermal Maximum (PETM or ETM1), H1 (or ETM2), H2, I1, and I2 - are marked by a carbon isotope excursion (CIE) within both marine and terrestrial sediments. The magnitude of CIE, which is a function of the amount and isotopic composition of carbon added to the ocean-atmosphere system, varies significantly between marine versus terrestrial substrates. Here we use the increase in carbon isotope fractionation by C3 land plants in response to increased pCO2 to reconcile this difference and reconstruct a range of background pCO2 and peak pCO2 for each CIE, provided two potential carbon sources: methane hydrate destabilization and permafrost-thawing/organic matter oxidation. Although the uncertainty on each pCO2 estimate using this approach is low (e.g., median uncertainty = + 23% / - 18%), this work highlights the potential for significant systematic bias in the pCO2 estimate resulting from sampling resolution, substrate type, diagenesis, and environmental change. Careful consideration of each of these factors is required especially when applying this approach to a single marine-terrestrial CIE pair. Given these limitations, we provide an upper estimate for background early Eocene pCO2 of 463 +248/-131 ppmv (methane hydrate scenario) to 806 +127/-104 ppmv (permafrost-thawing/organic matter oxidation scenario). These results, which represent the first pCO2 proxy estimates directly tied to the Eocene hyperthermals, demonstrate that early Eocene warmth was supported by background pCO2 less than ∼3.5× preindustrial levels and that pCO2 > 1000 ppmv may have occurred only briefly, during hyperthermal events.

  20. Seasonal Variations of Atmospheric CO2 over Fire Affected Regions Based on GOSAT Observations

    NASA Astrophysics Data System (ADS)

    Shi, Y.; Matsunaga, T.

    2016-12-01

    Abstract: The carbon dioxide (CO2) emissions released from biomass burning significantly affect the temporal variations of atmospheric CO2 concentrations. Based on a long-term (July 2009-June 2015) retrieved datasets by the Greenhouse Gases Observing Satellite (GOSAT), the seasonal cycle and interannual variations of column-averaged volume mixing ratios of atmospheric carbon dioxide (XCO2) in four fire affected continental regions were investigated. The results showed Northern Africa had the largest seasonal variations after removing its regional long-term trend of XCO2 with peak-to-peak amplitude of 6.2 ppm within the year, higher than central South America (2.4 ppm), Southern Africa (3.8 ppm) and Australia (1.7 ppm). The detrended regional XCO2 was found to be positively correlated with the fire CO2 emissions during fire activity period and negatively correlated with vegetation photosynthesis activity with different seasonal variabilities. Northern Africa recorded the largest change of seasonal variations of detrended XCO2 with a total of 12.8 ppm during fire seasons, higher than central South America, Southern Africa and Australia with 5.4 ppm, 6.7 ppm and 2.2 ppm, respectively. During fire episode, the positive detrended XCO2 was noticed during June-November in central South America, December-June in Northern Africa, May-November in Southern Africa. The Pearson correlation coefficients between the variations of detrended XCO2 and fire CO2 emissions from GFED4 (Global Fire Emissions Database v4) achieved best correlations in Southern Africa (R=0.77, p<0.05). Meanwhile, Southern Africa also experienced a significant negative relationship between the variations of detrended XCO2 and vegetation activity (R=-0.84, p<0.05). This study revealed that fire CO2 emissions and vegetation activity contributed greatly to the seasonal variations of GOSAT XCO2 dataset.

  1. [Characteristics of atmospheric CO2 concentration and variation of carbon source & sink at Lin'an regional background station].

    PubMed

    Pu, Jing-Jiao; Xu, Hong-Hui; Kang, Li-Li; Ma, Qian-Li

    2011-08-01

    Characteristics of Atmospheric CO2 concentration obtained by Flask measurements were analyzed at Lin'an regional background station from August 2006 to July 2009. According to the simulation results of carbon tracking model, the impact of carbon sources and sinks on CO2 concentration was evaluated in Yangtze River Delta. The results revealed that atmospheric CO2 concentrations at Lin'an regional background station were between 368.3 x 10(-6) and 414.8 x 10(-6). The CO2 concentration varied as seasons change, with maximum in winter and minimum in summer; the annual difference was about 20.5 x 10(-6). The long-term trend of CO2 concentration showed rapid growth year by year; the average growth rate was about 3.2 x 10(-6)/a. CO2 flux of Yangtze River Delta was mainly contributed by fossil fuel burning, terrestrial biosphere exchange and ocean exchange, while the contribution of fire emission was small. CO2 flux from fossil fuel burning played an important role in carbon source; terrestrial biosphere and ocean were important carbon sinks in this area. Seasonal variations of CO2 concentration at Lin'an regional background station were consistent with CO2 fluxes from fossil fuel burning and terrestrial biosphere exchange.

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

    USGS Publications Warehouse

    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

  3. Infrared heterodyne spectroscopy of atmospheric ozone

    NASA Technical Reports Server (NTRS)

    Frerking, M. A.; Muehlner, D. J.

    1977-01-01

    The absorption spectrum of atmospheric ozone is measured within a 1/cm region at 1100/cm, using an IR heterodyne detector (spectrometer with CO2 local oscillator) developed for astronomical work. Absorption spectra obtained by passing radiation from the tunable diode laser through an absorption cell, heterodyne spectra of atmospheric ozone, and a predicted atmospheric spectrum are compared. Water vapor absorbing in the region of interest (1100/cm) is also considered. Preliminary results encourage the use of diode laser local oscillators in tunable heterodyne detector systems for spectroscopy of atmospheric ozone and remote high-resolution spectroscopy of atmospheric constituents and pollutants.

  4. Phosphorus feedbacks constraining tropical ecosystem responses to changes in atmospheric CO2 and climate

    NASA Astrophysics Data System (ADS)

    Yang, Xiaojuan; Thornton, Peter E.; Ricciuto, Daniel M.; Hoffman, Forrest M.

    2016-07-01

    The effects of phosphorus (P) availability on carbon (C) cycling in the Amazon region are investigated using CLM-CNP. We demonstrate that the coupling of P dynamics reduces the simulated historical terrestrial C sink due to increasing atmospheric CO2 concentrations ([CO2]) by about 26%. Our exploratory simulations show that the response of tropical forest C cycling to increasing [CO2] depends on how elevated CO2 affects phosphatase enzyme production. The effects of warming are more complex, depending on the interactions between humidity, C, and nutrient dynamics. While a simulation with low humidity generally shows the reduction of net primary productivity (NPP), a second simulation with higher humidity suggests overall increases in NPP due to the dominant effects of reduced water stress and more nutrient availability. Our simulations point to the need for (1) new observations on how elevated [CO2] affects phosphatase enzyme production and (2) more tropical leaf-scale measurements under different temperature/humidity conditions with different soil P availability.

  5. TDLAS a laser diode sensor for the in situ monitoring of H2O, CO2 and their isotopes in the Martian atmosphere

    NASA Astrophysics Data System (ADS)

    Le Barbu, T.; Vinogradov, I.; Durry, G.; Korablev, O.; Chassefière, E.; Bertaux, J.-L.

    2006-01-01

    Within the framework of Pasteur-Exomars, we have proposed to measure in situ water vapor (H2O, HDO, H218O, H217O) and carbon dioxide (CO2, 13C16O2, 16O12C18O, 16O12C17O) isotopes and also CO, CH4 and N2O by absorption spectroscopy using near infrared laser diodes. The Service d’Aéronomie has a relevant experience in trace-gas detection with laser diodes. We have developed, with the support of the CNES and the CNRS, the SDLA diode laser spectrometer to measure in situ H2O (at 1.39 μm), CH4 (1.65 μm) and CO2 (at 1.60 μm) in the middle atmosphere from stratospheric balloons. The concentrations are obtained with a precision error of a few percent and with a high temporal resolution that ranges from 10 ms to 1 s. The developed laser probing technique should be also highly efficient to study the Martian atmosphere as there are much higher amounts of water vapor and carbon dioxide in the Martian atmosphere than in the lower stratosphere (H2O: 200 ppmv at 6 hPa on Mars, 5 ppmv at 10 hPa in the low stratosphere (LS); CO2 95% on Mars, 360 ppmv in the LS). Hence, we propose to adapt the laser probing technique to the Martian atmosphere. The main objectives are to determine water vapor and carbon dioxide fluxes and to study boundary layer properties. The sensor will provide in situ daily, diurnally resolved measurements of near-surface H2O and CO2 concentrations over seasonal time scales. The additional isotopic measurements will provide quantitative constraints on the evolution of atmospheric composition and on the history of water on Mars.

  6. A Database of Woody Vegetation Responses to Elevated Atmospheric CO2 (NDP-072)

    DOE Data Explorer

    Curtis, Peter S [The Ohio State Univ., Columbus, OH (United States); Cushman, Robert M [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Brenkert, Antoinette L [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States)

    1999-01-01

    To perform a statistically rigorous meta-analysis of research results on the response by woody vegetation to increased atmospheric CO2 levels, a multiparameter database of responses was compiled. Eighty-four independent CO2-enrichment studies, covering 65 species and 35 response parameters, met the necessary criteria for inclusion in the database: reporting mean response, sample size, and variance of the response (either as standard deviation or standard error). Data were retrieved from the published literature and unpublished reports. This numeric data package contains a 29-field data set of CO2-exposure experiment responses by woody plants (as both a flat ASCII file and a spreadsheet file), files listing the references to the CO2-exposure experiments and specific comments relevant to the data in the data set, and this documentation file (which includes SAS and Fortran codes to read the ASCII data file; SAS is a registered trademark of the SAS Institute, Inc., Cary, North Carolina 27511).

  7. Progress and Challenges in Predicting Crop Responses to Atmospheric [CO2

    NASA Astrophysics Data System (ADS)

    Kent, J.; Paustian, K.

    2017-12-01

    Increasing atmospheric [CO2] directly accelerates photosynthesis in C3 crops, and indirectly promotes yields by reducing stomatal conductance and associated water losses in C3 and C4 crops. Several decades of experiments have exposed crops to eCO2 in greenhouses and other enclosures and observed yield increases on the order of 33%. FACE systems were developed in the early 1990s to better replicate open-field growing conditions. Some authors contend that FACE results indicate lower crop yield responses than enclosure studies, while others maintain no significant difference or attribute differences to various methodological factors. The crop CO2 response processes in many crop models were developed using results from enclosure experiments. This work tested the ability of one such model, DayCent, to reproduce crop responses to CO2 enrichment from several FACE experiments. DayCent performed well at simulating yield and transpiration responses in C4 crops, but significantly overestimated yield responses in C3 crops. After adjustment of CO2-response parameters, DayCent was able to reproduce mean yield responses for specific crops. However, crop yield responses from FACE experiments vary widely across years and sites, and likely reflect complex interactions between conditions such as weather, soils, cultivars, and biotic stressors. Further experimental work is needed to identify the secondary variables that explain this variability so that models can more reliably forecast crop yields under climate change. Likewise, CO2 impacts on crop outcomes such as belowground biomass allocation and grain N content have implications for agricultural C fluxes and human nutrition, respectively, but are poorly understood and thus difficult to simulate with confidence.

  8. Effects of Long-Term CO2 Enrichment on Soil-Atmosphere CH4 Fluxes and the Spatial Micro-Distribution of Methanotrophic Bacteria.

    PubMed

    Karbin, Saeed; Guillet, Cécile; Kammann, Claudia I; Niklaus, Pascal A

    2015-01-01

    Effects of elevated atmospheric CO2 concentrations on plant growth and associated C cycling have intensively been studied, but less is known about effects on the fluxes of radiatively active trace gases other than CO2. Net soil-atmosphere CH4 fluxes are determined by the balance of soil microbially-driven methane (CH4) oxidation and methanogenesis, and both might change under elevated CO2. Here, we studied CH4 dynamics in a permanent grassland exposed to elevated CO2 for 14 years. Soil-atmosphere fluxes of CH4 were measured using large static chambers, over a period of four years. The ecosystem was a net sink for atmospheric CH4 for most of the time except summer to fall when net CH4 emissions occurred. We did not detect any elevated CO2 effects on CH4 fluxes, but emissions were difficult to quantify due to their discontinuous nature, most likely because of ebullition from the saturated zone. Potential methanotrophic activity, determined by incubation of fresh sieved soil under standardized conditions, also did not reveal any effect of the CO2 treatment. Finally, we determined the spatial micro-distribution of methanotrophic activity at less than 5× atmospheric (10 ppm) and elevated (10000 ppm) CH4 concentrations, using a novel auto-radiographic technique. These analyses indicated that domains of net CH4 assimilation were distributed throughout the analyzed top 15 cm of soils, with no dependence on CH4 concentration or CO2 treatment. Our investigations suggest that elevated CO2 exerts no or only minor effects on CH4 fluxes in the type of ecosystem we studied, at least as long as soil moisture differences are small or absent as was the case here. The autoradiographic analyses further indicate that the spatial niche of CH4 oxidation does not shift in response to CO2 enrichment or CH4 concentration, and that the same type of methanotrophs may oxidize CH4 from atmospheric and soil-internal sources.

  9. Soil organic carbon dust emission: an omitted global source of atmospheric CO2?

    USDA-ARS?s Scientific Manuscript database

    Soil erosion redistributes soil organic carbon (SOC) within terrestrial ecosystems, to the atmosphere and oceans. Dust export is an essential component of the carbon (C) and carbon dioxide (CO2) budget because wind erosion contributes to the C cycle by removing selectively SOC from vast areas and tr...

  10. Effect of photosynthesis on the abundance of 18O13C16O in atmospheric CO2

    NASA Astrophysics Data System (ADS)

    Hofmann, Magdalena E. G.; Pons, Thijs L.; Ziegler, Martin; Lourens, Lucas J.; Röckmann, Thomas

    2016-04-01

    The abundance of the isotopologue 18O13C16O (Δ47) in atmospheric air is a promising new tracer for the atmospheric carbon cycle (Eiler and Schauble, 2004; Affek and Eiler, 2006; Affek et al., 2007). The large gross fluxes in CO2 between the atmosphere and biosphere are supposed to play a major role in controlling its abundance. Eiler and Schauble (2004) set up a box model describing the effect of air-leaf interaction on the abundance of 18O13C16O in atmospheric air. The main assumption is that the exchange between CO2 and water within the mesophyll cells will imprint a Δ47 value on the back-diffusing CO2 that reflects the leaf temperature. Additionally, kinetic effects due to CO2 diffusion into and out of the stomata are thought to play a role. We investigated the effect of photosynthesis on the residual CO2 under controlled conditions using a leaf chamber set-up to quantitatively test the model assumptions suggested by Eiler and Schauble (2004). We studied the effect of photosynthesis on the residual CO2 using two C3 and one C4 plant species: (i) sunflower (Helianthus annuus), a C3 species with a high leaf conductance for CO2 diffusion, (ii) ivy (Hedera hibernica), a C3 species with a low conductance, and (iii), maize (Zea mays), a species with the C4 photosynthetic pathway. We also investigated the effect of different light intensities (photosynthetic photon flux density of 200, 700 and 1800 μmol m2s-1), and thus, photosynthetic rate in sunflower and maize. A leaf was mounted in a cuvette with a transparent window and an adjustable light source. The air inside was thoroughly mixed, making the composition of the outgoing air equal to the air inside. A gas-mixing unit was attached at the entrance of the cuvette that mixed air with a high concentration of scrambled CO2 with a Δ47 value of 0 to 0.1‰ with CO2 free air to set the CO2 concentration of ingoing air at 500 ppm. The flow rate through the cuvette was adjusted to the photosynthetic activity of the leaf

  11. Characteristics of the atmospheric CO2 signal as observed over the conterminous United States during INTEX-NA

    NASA Astrophysics Data System (ADS)

    Choi, Yonghoon; Vay, Stephanie A.; Vadrevu, Krishna P.; Soja, Amber J.; Woo, Jung-Hun; Nolf, Scott R.; Sachse, Glen W.; Diskin, Glenn S.; Blake, Donald R.; Blake, Nicola J.; Singh, Hanwant B.; Avery, Melody A.; Fried, Alan; Pfister, Leonhard; Fuelberg, Henry E.

    2008-04-01

    High resolution in situ measurements of atmospheric CO2 were made from the NASA DC-8 aircraft during the Intercontinental Chemical Transport Experiment-North America (INTEX-NA) campaign, part of the wider International Consortium for Atmospheric Research on Transport and Transformation (ICARTT). During the summer of 2004, eighteen flights comprising 160 h of measurements were conducted within a region bounded by 27 to 53°N and 36 to 139°W over an altitude range of 0.15 to 12 km. These large-scale surveys provided the opportunity to examine the characteristics of the atmospheric CO2 signal over sparsely sampled areas of North America and adjacent ocean basins. The observations showed a high degree of variability (≤18%) due to the myriad source and sink processes influencing the air masses intercepted over the INTEX-NA sampling domain. Surface fluxes had strong effects on continental scale concentration gradients. Clear signatures of CO2 uptake were seen east of the Mississippi River, notably a persistent CO2 deficit in the lowest 2-3 km. When combining the airborne CO2 measurements with LANDSAT and MODIS data products, the lowest CO2 mixing ratios observed during the campaign (337 ppm) were tied to mid-continental agricultural fields planted in corn and soybeans. We used simultaneous measurements of CO, O3, C2Cl4, C2H6, C2H2 and other unique chemical tracers to differentiate air mass types. Coupling these distinct air mass chemical signatures with transport history permitted identification of convection, stratosphere-troposphere exchange, long-range transport from Eastern Asia, boreal wildfires, and continental outflow as competing processes at multiple scales influencing the observed concentrations. Our results suggest these are important factors contributing to the large-scale distribution in CO2 mixing ratios thus these observations offer new constraints in the computation of the North American carbon budget.

  12. Airborne & Ground-based measurements of atmospheric CO2 using the 1.57-μm laser absorption spectrometer

    NASA Astrophysics Data System (ADS)

    Sakaizawa, D.; Kawakami, S.; Nakajima, M.; Tanaka, T.; Miyamoto, Y.; Morino, I.; Uchino, O.; Asai, K.

    2009-12-01

    Greenhouse gases observing satellite (GOSAT) started the measurement of global CO2 abundances to reveal its continental inventory using two passive remote sensors. The goal that the sensor needs to be done is to achieve an 1% relative accuracy in order to reduce uncertainties of CO2 budget. Nevertheless, in the future global CO2 monitoring, more accurate measurement of global tropospheric CO2 abundances with the monthly regional scale are required to improve the knowledge of CO2 exchanges among the land, ocean, and atmosphere. In order to fulfill demands, a laser remote sensor, such as DIAL or laser absorption spectrometer (LAS), is a potential candidate of future space-based missions. Nowadays, those technologies are required to demonstrate an accuracy of the few-ppm level through airborne & ground-based measurements. We developed the prototype of the 1.57um LAS for a step of the next missions and perform it at the ground-based and airborne platform to show the properly validated performance in the framework of GOSAT validation. Our CO2 LAS is consisted of all optical fiber circuits & compact receiving /transmitting optics to achieve the portable, flexible and rigid system. The optical sources of on- and off-line are distributed feedback lasers, which are tuned at the strong and weak position of the R12 line in the (30012<-00001) absorption band. Their fiber coupled outputs are sinusoidal amplitude modulated by each EO devices with kHz rate and combined and amplified using an erbium doped fiber amplifier. Scattered signals from the hard target are collected by the 11cm receiving telescope and detected and stored into the laptop computer. After that, we evaluated the atmospheric CO2 density using the meteorological parameters and ratio between the on- and off-line signals. The resultant of the ground-based measurement of 3km optical length indicated that the statistical error of the path averaged atmospheric CO2 density is less than 2.8ppm with 25 minutes averaging

  13. The impact of temperature dependent CO2 cross section measurements: A role for heterogeneous chemistry in the atmosphere of Mars?

    NASA Technical Reports Server (NTRS)

    Anbar, A. D.; Allen, M.; Nair, H.; Leu, M-T.; Yung, Y. L.

    1992-01-01

    Carbon dioxide comprises over 95 percent of the Mars atmosphere, despite continuous photolysis of CO2 by solar ultraviolet (UV) radiation. Since the direct recombination of CO and O is spinforbidden, the chemical stability of CO2 in the Martian atmosphere is thought to be the result of a HO(x)-catalyzed recombination scheme. Thus the rate of CO oxidation is sensitive to the abundance and altitude distribution of OH, H, and HO2. Most Martian atmospheric models assume that HO(x) abundances are governed purely by gas phase chemistry. However, it is well established that reactive HO(x) radical are adsorbed by a wide variety of surfaces. The authors have combined laboratory studies of H, OH, and HO2 adsorption on inorganic surfaces, observational data of aerosol distributions, and an updated photochemical model to demonstrate that adsorption on either dust or ice aerosols is capable of reducing HO(x) abundances significantly, thereby retarding the rate of CO oxidation.

  14. Rising atmospheric CO2 leads to large impact of biology on Southern Ocean CO2 uptake via changes of the Revelle factor

    PubMed Central

    Hauck, J; Völker, C

    2015-01-01

    The Southern Ocean is a key region for global carbon uptake and is characterized by a strong seasonality with the annual CO2 uptake being mediated by biological carbon drawdown in summer. Here we show that the contribution of biology to CO2 uptake will become even more important until 2100. This is the case even if biological production remains unaltered and can be explained by the decreasing buffer capacity of the ocean as its carbon content increases. The same amount of biological carbon drawdown leads to a more than twice as large reduction in CO2(aq) concentration and hence to a larger CO2 gradient between ocean and atmosphere that drives the gas exchange. While the winter uptake south of 44°S changes little, the summer uptake increases largely and is responsible for the annual mean response. The combination of decreasing buffer capacity and strong seasonality of biological carbon drawdown introduces a strong and increasing seasonality in the anthropogenic carbon uptake. Key Points Decrease of buffer capacity leads to stronger summer CO2 uptake in the future Biology will contribute more to future CO2 uptake in Southern Ocean Seasonality affects anthropogenic carbon uptake strongly PMID:26074650

  15. [Determination of net exchange of CO2 between paddy fields and atmosphere with static poaque-chamber-based measurements].

    PubMed

    Zheng, Xunhua; Xu, Zhongjun; Wang, Yuesi; Han, Shenghui; Huang, Yao; Cai, Zucong; Zhu, Jianguo

    2002-10-01

    We firstly introduced the method for determining the net ecosystem exchange fluxes of CO2 (NEE) between croplands and atmosphere, based on field measurements using static opaquechamber/gas chromatography methods was introduced, and the application of this method in the FACE (free-air CO2 enrichment) study to examine the effects of elevated CO2 on the NEE over a typical paddy ecosystem was carried out, because of lacking in observation data for some necessary parameters, e.g., dark maintenance respiration coefficient, only the minimum value of NEE (NEEmin) was calculated based on opaque-chamber measurements. The NEEmin data indicate that CO2 elevated by 200 +/- 40 mumol.mol-1 significantly increased the ecosystem uptake of atmospheric CO2 by a factor ca. 3. To accurately determine the NEE based on opaquechamber measurements, dark maintenance respiration coefficient, above-ground biomass and root: shoot, i.e. R:S, ratio of root to shoot should be observed over the whole growing season.

  16. Water relations in grassland and desert ecosystems exposed to elevated atmospheric CO2.

    PubMed

    Morgan, J A; Pataki, D E; Körner, C; Clark, H; Del Grosso, S J; Grünzweig, J M; Knapp, A K; Mosier, A R; Newton, P C D; Niklaus, P A; Nippert, J B; Nowak, R S; Parton, W J; Polley, H W; Shaw, M R

    2004-06-01

    Atmospheric CO2 enrichment may stimulate plant growth directly through (1) enhanced photosynthesis or indirectly, through (2) reduced plant water consumption and hence slower soil moisture depletion, or the combination of both. Herein we describe gas exchange, plant biomass and species responses of five native or semi-native temperate and Mediterranean grasslands and three semi-arid systems to CO2 enrichment, with an emphasis on water relations. Increasing CO2 led to decreased leaf conductance for water vapor, improved plant water status, altered seasonal evapotranspiration dynamics, and in most cases, periodic increases in soil water content. The extent, timing and duration of these responses varied among ecosystems, species and years. Across the grasslands of the Kansas tallgrass prairie, Colorado shortgrass steppe and Swiss calcareous grassland, increases in aboveground biomass from CO2 enrichment were relatively greater in dry years. In contrast, CO2-induced aboveground biomass increases in the Texas C3/C4 grassland and the New Zealand pasture seemed little or only marginally influenced by yearly variation in soil water, while plant growth in the Mojave Desert was stimulated by CO2 in a relatively wet year. Mediterranean grasslands sometimes failed to respond to CO2-related increased late-season water, whereas semiarid Negev grassland assemblages profited. Vegetative and reproductive responses to CO2 were highly varied among species and ecosystems, and did not generally follow any predictable pattern in regard to functional groups. Results suggest that the indirect effects of CO2 on plant and soil water relations may contribute substantially to experimentally induced CO2-effects, and also reflect local humidity conditions. For landscape scale predictions, this analysis calls for a clear distinction between biomass responses due to direct CO2 effects on photosynthesis and those indirect CO2 effects via soil moisture as documented here.

  17. The global pyrogenic carbon cycle and its impact on the level of atmospheric CO2 over past and future centuries.

    PubMed

    Landry, Jean-Sébastien; Matthews, H Damon

    2017-08-01

    The incomplete combustion of vegetation and dead organic matter by landscape fires creates recalcitrant pyrogenic carbon (PyC), which could be consequential for the global carbon budget if changes in fire regime, climate, and atmospheric CO 2 were to substantially affect gains and losses of PyC on land and in oceans. Here, we included global PyC cycling in a coupled climate-carbon model to assess the role of PyC in historical and future simulations, accounting for uncertainties through five sets of parameter estimates. We obtained year-2000 global stocks of (Central estimate, likely uncertainty range in parentheses) 86 (11-154), 47 (2-64), and 1129 (90-5892) Pg C for terrestrial residual PyC (RPyC), marine dissolved PyC, and marine particulate PyC, respectively. PyC cycling decreased atmospheric CO 2 only slightly between 1751 and 2000 (by 0.8 Pg C for the Central estimate) as PyC-related fluxes changed little over the period. For 2000 to 2300, we combined Representative Concentration Pathways (RCPs) 4.5 and 8.5 with stable or continuously increasing future fire frequencies. For the increasing future fire regime, the production of new RPyC generally outpaced the warming-induced accelerated loss of existing RPyC, so that PyC cycling decreased atmospheric CO 2 between 2000 and 2300 for most estimates (by 4-8 Pg C for Central). For the stable fire regime, however, PyC cycling usually increased atmospheric CO 2 (by 1-9 Pg C for Central), and only the most extreme choice of parameters maximizing PyC production and minimizing PyC decomposition led to atmospheric CO 2 decreases under RCPs 4.5 and 8.5 (by 5-8 Pg C). Our results suggest that PyC cycling will likely reduce the future increase in atmospheric CO 2 if landscape fires become much more frequent; however, in the absence of a substantial increase in fire frequency, PyC cycling might contribute to, rather than mitigate, the future increase in atmospheric CO 2 . © 2016 John Wiley & Sons Ltd.

  18. Strong regional atmospheric 14C signature of respired CO 2 observed from a tall tower over the midwestern United States

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    LaFranchi, B. W.; McFarlane, K. J.; Miller, J. B.

    Radiocarbon in CO 2 ( 14CO 2) measurements can aid in discriminating between fast (<1 year) and slower (>5–10 years) cycling of C between the atmosphere and the terrestrial biosphere due to the 14C disequilibrium between atmospheric and terrestrial C. However, 14CO 2 in the atmosphere is typically much more strongly impacted by fossil fuel emissions of CO 2, and, thus, observations often provide little additional constraints on respiratory flux estimates at regional scales. Here we describe a data set of 14CO 2 observations from a tall tower in northern Wisconsin (USA) where fossil fuel influence is far enough removedmore » that during the summer months, the biospheric component of the 14CO 2 budget dominates. We find that the terrestrial biosphere is responsible for a significant contribution to 14CO 2 that is 2–3 times higher than predicted by the Carnegie-Ames-Stanford approach terrestrial ecosystem model for observations made in 2010. This likely includes a substantial contribution from the North American boreal ecoregion, but transported biospheric emissions from outside the model domain cannot be ruled out. The 14CO 2 enhancement also appears somewhat decreased in observations made over subsequent years, suggesting that 2010 may be anomalous. Furthermore, with these caveats acknowledged, we discuss the implications of the observation/model comparison in terms of possible systematic biases in the model versus short-term anomalies in the observations. Going forward, this isotopic signal could be exploited as an important indicator to better constrain both the long-term carbon balance of terrestrial ecosystems and the short-term impact of disturbance-based loss of carbon to the atmosphere.« less

  19. Strong regional atmospheric 14C signature of respired CO 2 observed from a tall tower over the midwestern United States

    DOE PAGES

    LaFranchi, B. W.; McFarlane, K. J.; Miller, J. B.; ...

    2016-08-31

    Radiocarbon in CO 2 ( 14CO 2) measurements can aid in discriminating between fast (<1 year) and slower (>5–10 years) cycling of C between the atmosphere and the terrestrial biosphere due to the 14C disequilibrium between atmospheric and terrestrial C. However, 14CO 2 in the atmosphere is typically much more strongly impacted by fossil fuel emissions of CO 2, and, thus, observations often provide little additional constraints on respiratory flux estimates at regional scales. Here we describe a data set of 14CO 2 observations from a tall tower in northern Wisconsin (USA) where fossil fuel influence is far enough removedmore » that during the summer months, the biospheric component of the 14CO 2 budget dominates. We find that the terrestrial biosphere is responsible for a significant contribution to 14CO 2 that is 2–3 times higher than predicted by the Carnegie-Ames-Stanford approach terrestrial ecosystem model for observations made in 2010. This likely includes a substantial contribution from the North American boreal ecoregion, but transported biospheric emissions from outside the model domain cannot be ruled out. The 14CO 2 enhancement also appears somewhat decreased in observations made over subsequent years, suggesting that 2010 may be anomalous. Furthermore, with these caveats acknowledged, we discuss the implications of the observation/model comparison in terms of possible systematic biases in the model versus short-term anomalies in the observations. Going forward, this isotopic signal could be exploited as an important indicator to better constrain both the long-term carbon balance of terrestrial ecosystems and the short-term impact of disturbance-based loss of carbon to the atmosphere.« less

  20. Strong regional atmospheric 14C signature of respired CO2 observed from a tall tower over the midwestern United States

    NASA Astrophysics Data System (ADS)

    LaFranchi, B. W.; McFarlane, K. J.; Miller, J. B.; Lehman, S. J.; Phillips, C. L.; Andrews, A. E.; Tans, P. P.; Chen, H.; Liu, Z.; Turnbull, J. C.; Xu, X.; Guilderson, T. P.

    2016-08-01

    Radiocarbon in CO2 (14CO2) measurements can aid in discriminating between fast (<1 year) and slower (>5-10 years) cycling of C between the atmosphere and the terrestrial biosphere due to the 14C disequilibrium between atmospheric and terrestrial C. However, 14CO2 in the atmosphere is typically much more strongly impacted by fossil fuel emissions of CO2, and, thus, observations often provide little additional constraints on respiratory flux estimates at regional scales. Here we describe a data set of 14CO2 observations from a tall tower in northern Wisconsin (USA) where fossil fuel influence is far enough removed that during the summer months, the biospheric component of the 14CO2 budget dominates. We find that the terrestrial biosphere is responsible for a significant contribution to 14CO2 that is 2-3 times higher than predicted by the Carnegie-Ames-Stanford approach terrestrial ecosystem model for observations made in 2010. This likely includes a substantial contribution from the North American boreal ecoregion, but transported biospheric emissions from outside the model domain cannot be ruled out. The 14CO2 enhancement also appears somewhat decreased in observations made over subsequent years, suggesting that 2010 may be anomalous. With these caveats acknowledged, we discuss the implications of the observation/model comparison in terms of possible systematic biases in the model versus short-term anomalies in the observations. Going forward, this isotopic signal could be exploited as an important indicator to better constrain both the long-term carbon balance of terrestrial ecosystems and the short-term impact of disturbance-based loss of carbon to the atmosphere.

  1. 2-micron Pulsed Direct Detection IPDA Lidar for Atmospheric CO2 Measurements

    NASA Astrophysics Data System (ADS)

    Yu, J.; Singh, U.; Petros, M.

    2012-12-01

    A 2-micron high energy, pulsed Integrated Path Differential Absorption (IPDA) lidar is being developed for atmospheric CO2 measurements. Development of this lidar heavily leverages the 2-micron laser technologies developed in LaRC over the last decade. The high pulse energy, direct detection lidar operating at CO2 2-micron absorption band provides an alternate approach to measure CO2 concentrations with significant advantages. It is expected to provide high-precision measurement capability by unambiguously eliminating contamination from aerosols and clouds that can bias the IPDA measurement. Our objective is to integrate an existing high energy double-pulsed 2-micron laser transmitter with a direct detection receiver and telescope to enable an airborne capability to perform a first proof of principle demonstration of airborne direct detection CO2 measurements. The 2-micron transmitter provides 100mJ at 10Hz with double pulse format specifically designed for DIAL/IPDA instrument. The compact, rugged, highly reliable transceiver is based on unique Ho:Tm:YLF high-energy 2-micron pulsed laser technology. All the optical mounts are custom designed and have space heritage. A 16-inch diameter telescope has been designed and being manufactured for the direct detection lidar. The detector is an InGaAs Positive-Intrinsic-Negative (PIN) photodiode manufactured by Hamamatsu Corporation. The performance of the detector is characterized at various operating temperatures and bias voltages for spectral response, NEP, response time, dynamic range, and linearity. A collinear lidar structure is designed to be integrated to NASA UC12 or B200 research aircrafts. This paper will describe the design of the airborne 2-micron pulsed IPDA lidar system; the lidar operation parameters; the wavelength pair selection; laser transmitter energy, pulse rate, beam divergence, double pulse generation and accurate frequency control; detector characterization; telescope design; lidar structure design

  2. Modification of land-atmosphere interactions by CO2 effects: Implications for summer dryness and heat wave amplitude

    NASA Astrophysics Data System (ADS)

    Lemordant, Léo.; Gentine, Pierre; Stéfanon, Marc; Drobinski, Philippe; Fatichi, Simone

    2016-10-01

    Plant stomata couple the energy, water, and carbon cycles. We use the framework of Regional Climate Modeling to simulate the 2003 European heat wave and assess how higher levels of surface CO2 may affect such an extreme event through land-atmosphere interactions. Increased CO2 modifies the seasonality of the water cycle through stomatal regulation and increased leaf area. As a result, the water saved during the growing season through higher water use efficiency mitigates summer dryness and the heat wave impact. Land-atmosphere interactions and CO2 fertilization together synergistically contribute to increased summer transpiration. This, in turn, alters the surface energy budget and decreases sensible heat flux, mitigating air temperature rise. Accurate representation of the response to higher CO2 levels and of the coupling between the carbon and water cycles is therefore critical to forecasting seasonal climate, water cycle dynamics, and to enhance the accuracy of extreme event prediction under future climate.

  3. Atmospheric carbon dioxide concentrations before 2.2 billion years ago

    NASA Technical Reports Server (NTRS)

    Rye, R.; Kuo, P. H.; Holland, H. D.

    1995-01-01

    The composition of the Earth's early atmosphere is a subject of continuing debate. In particular, it has been suggested that elevated concentrations of atmospheric carbon dioxide would have been necessary to maintain normal surface temperatures in the face of lower solar luminosity in early Earth history. Fossil weathering profiles, known as palaeosols, have provided semi-quantitative constraints on atmospheric oxygen partial pressure (pO2) before 2.2 Gyr ago. Here we use the same well studied palaeosols to constrain atmospheric pCO2 between 2.75 and 2.2 Gyr ago. The observation that iron lost from the tops of these profiles was reprecipitated lower down as iron silicate minerals, rather than as iron carbonate, indicates that atmospheric pCO2 must have been less than 10(-1.4) atm--about 100 times today's level of 360 p.p.m., and at least five times lower than that required in one-dimensional climate models to compensate for lower solar luminosity at 2.75 Gyr. Our results suggest that either the Earth's early climate was much more sensitive to increases in pCO2 than has been thought, or that one or more greenhouse gases other than CO2 contributed significantly to the atmosphere's radiative balance during the late Archaean and early Proterozoic eons.

  4. Monitoring of leaked CO2 through sediment, water column and atmosphere in sub-seabed CCS experiment

    NASA Astrophysics Data System (ADS)

    Shitashima, K.; Sakamoto, A.; Maea, Y.

    2013-12-01

    CO2 capture and storage in sub-seabed geological formations (sub-seabed CCS) is currently being studied as a feasible option to mitigate the accumulation of anthropogenic CO2 in the atmosphere. In implementing sub-seabed CCS, detecting and monitoring the impact of the sequestered CO2 on the ocean environment is highly important. The first controlled CO2 release experiment, entitled 'Quantifying and Monitoring Potential Ecosystem Impacts of Geological Carbon Storage (QICS)', took place in Ardmucknish Bay, Oban, in May-July 2012. We applied the in-situ pH/pCO2/ORP sensor to the QICS experiment for detection and monitoring of leaked CO2, and carried out several observations. The on-line sensor that was connected by 400m of RS422 cable was deployed close to the CO2 leakage (bubbling) point, and the fluctuations of pH, pCO2 and ORP were monitored in real-time in a observation van on land. Three sets of off-line sensors were also placed on seafloor in respective points (release point, and two low impacted regions at 25m and 75m distant) for three months. The long-term monitoring of pH in sediment at 50cm depth under the seafloor was conducted. The spear type electrode was stabbed into sediment by diver near the CO2 leakage point. Wide-area mapping surveys of pH, pCO2 and ORP in seawater around the leakage point were carried out by AUV (REMUS-100) that some chemical sensors were installed in. The AUV cruised along the grid line in two layers of 4m and 2m above the seafloor during both of periods of low tide and high tide. Atmospheric CO2 in sea surface above the leakage point was observed by the LI-COR CO2 Analyzer. The analyzer was attached to the bow of ship, and the ship navigated a wide-area along a grid observation line during both of periods of low tide and high tide.

  5. Atmospheric CO2 Concentrations--The Canadian Background Air Pollution Monitoring Network (1993) (NDP-034)

    DOE Data Explorer

    Trivett, N. B. A. [Environment Canada, Atmospheric Environment Service, Downsview, Ontario, Canada; Hudec, V. C. [Environment Canada, Atmospheric Environment Service, Downsview, Ontario, Canada; Wong, C. S. [Marine Carbon Research Centre, Institute of Ocean Sciences, Sidney, British Columbia, Canada

    1993-01-01

    Flask air samples collected at roughly weekly intervals at three Canadian sites [Alert, Northwest Territories (July 1975 through July 1992); Sable Island, Nova Scotia (March 1975 through July 1992); and Cape St. James, British Columbia (May 1979 through July 1992)] were analyzed for CO2 concentration with the measurements directly traceable to the WMO primary CO2 standards. Each record includes the date, atmospheric CO2 concentration, and flask classification code. They provide an accurate record of CO2 concentration levels in Canada during the past two decades. Because these data are directly traceable to WMO standards, this record may be compared with records from other Background Air Pollution Monitoring Network (BAPMoN) stations. The data are in three files (one for each of the monitoring stations) ranging in size from 9.4 to 20.1 kB.

  6. A Ground-Based 2-Micron DIAL System to Profile Tropospheric CO2 and Aerosol Distributions for Atmospheric Studies

    NASA Technical Reports Server (NTRS)

    Ismail, Syed; Koch, Grady; Abedin, Nurul; Refaat, Tamer; Rubio, Manuel; Davis, Kenneth; Miller, Charles; Singh, Upendra

    2006-01-01

    System will operate at a temperature insensitive CO2 line (2050.967 nm) with side-line tuning and off-set locking. Demonstrated an order of magnitude improvement in laser line locking needed for high precision measurements, side-line operation, and simultaneously double pulsing and line locking. Detector testing of phototransistor has demonstrated sensitivity to aerosol features over long distances in the atmosphere and resolve features approx. 100m. Optical systems that collect light onto small area detectors work well. Receiver optical designs are being optimized and data acquisition systems developed. CO2 line parameter characterization in progress In situ sensor calibration in progress for validation of DIAL CO2 system.

  7. Historical carbonyl sulfide observations support long-term growth in atmospheric CO2 seasonal amplitude

    NASA Astrophysics Data System (ADS)

    Campbell, J. E.; Hilton, T. W.; Laine, M.; Wang, Y.; Berry, J. A.; Hannigan, J. W.

    2017-12-01

    The seasonal amplitude in atmospheric CO2 has grown over the last 50 years, pointing to a fundamental shift in the regional carbon cycle. Theoretical drivers from the amplitude growth include changes in terrestrial photosynthesis and heterotrophic respiration. However, large-scale, measurement-based evidence for these mechanisms is unclear. Here we analyze historical measurements of carbonyl sulfide which also show long-term growth in seasonal amplitude. We use this new trend to interpret the underlying mechanisms of CO2 amplitude growth and to validate global ecosystem models.

  8. Evaluating the Capacity of Global CO2 Flux and Atmospheric Transport Models to Incorporate New Satellite Observations

    NASA Technical Reports Server (NTRS)

    Kawa, S. R.; Collatz, G. J.; Erickson, D. J.; Denning, A. S.; Wofsy, S. C.; Andrews, A. E.

    2007-01-01

    As we enter the new era of satellite remote sensing for CO2 and other carbon cyclerelated quantities, advanced modeling and analysis capabilities are required to fully capitalize on the new observations. Model estimates of CO2 surface flux and atmospheric transport are required for initial constraints on inverse analyses, to connect atmospheric observations to the location of surface sources and sinks, and ultimately for future projections of carbon-climate interactions. For application to current, planned, and future remotely sensed CO2 data, it is desirable that these models are accurate and unbiased at time scales from less than daily to multi-annual and at spatial scales from several kilometers or finer to global. Here we focus on simulated CO2 fluxes from terrestrial vegetation and atmospheric transport mutually constrained by analyzed meteorological fields from the Goddard Modeling and Assimilation Office for the period 1998 through 2006. Use of assimilated meteorological data enables direct model comparison to observations across a wide range of scales of variability. The biospheric fluxes are produced by the CASA model at lxi degrees on a monthly mean basis, modulated hourly with analyzed temperature and sunlight. Both physiological and biomass burning fluxes are derived using satellite observations of vegetation, burned area (as in GFED-2), and analyzed meteorology. For the purposes of comparison to CO2 data, fossil fuel and ocean fluxes are also included in the transport simulations. In this presentation we evaluate the model's ability to simulate CO2 flux and mixing ratio variability in comparison to in situ observations at sites in Northern mid latitudes and the continental tropics. The influence of key process representations is inferred. We find that the model can resolve much of the hourly to synoptic variability in the observations, although there are limits imposed by vertical resolution of boundary layer processes. The seasonal cycle and its

  9. Mathematical Analysis of High-Temperature Co-electrolysis of CO2 and O2 Production in a Closed-Loop Atmosphere Revitalization System

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Michael G. McKellar; Manohar S. Sohal; Lila Mulloth

    2010-03-01

    NASA has been evaluating two closed-loop atmosphere revitalization architectures based on Sabatier and Bosch carbon dioxide, CO2, reduction technologies. The CO2 and steam, H2O, co-electrolysis process is another option that NASA has investigated. Utilizing recent advances in the fuel cell technology sector, the Idaho National Laboratory, INL, has developed a CO2 and H2O co-electrolysis process to produce oxygen and syngas (carbon monoxide, CO and hydrogen, H2 mixture) for terrestrial (energy production) application. The technology is a combined process that involves steam electrolysis, CO2 electrolysis, and the reverse water gas shift (RWGS) reaction. A number of process models have been developedmore » and analyzed to determine the theoretical power required to recover oxygen, O2, in each case. These models include the current Sabatier and Bosch technologies and combinations of those processes with high-temperature co-electrolysis. The cases of constant CO2 supply and constant O2 production were evaluated. In addition, a process model of the hydrogenation process with co-electrolysis was developed and compared. Sabatier processes require the least amount of energy input per kg of oxygen produced. If co-electrolysis replaces solid polymer electrolyte (SPE) electrolysis within the Sabatier architecture, the power requirement is reduced by over 10%, but only if heat recuperation is used. Sabatier processes, however, require external water to achieve the lower power results. Under conditions of constant incoming carbon dioxide flow, the Sabatier architectures require more power than the other architectures. The Bosch, Boudouard with co-electrolysis, and the hydrogenation with co-electrolysis processes require little or no external water. The Bosch and hydrogenation processes produce water within their reactors, which aids in reducing the power requirement for electrolysis. The Boudouard with co-electrolysis process has a higher electrolysis power requirement

  10. Marine biological controls on atmospheric CO2 and climate

    NASA Technical Reports Server (NTRS)

    Mcelroy, M. B.

    1983-01-01

    It is argued that the ocean is losing N gas faster than N is being returned to the ocean, and that replenishment of the N supply in the ocean usually occurs during ice ages. Available N from river and estruarine transport and from rainfall after formation by lightning are shown to be at a rate too low to compensate for the 10,000 yr oceanic lifetime of N. Ice sheets advance and transfer moraine N to the ocean, lower the sea levels, erode the ocean beds, promote greater biological productivity, and reduce CO2. Ice core samples have indicated a variability in the atmospheric N content that could be attributed to the ice age scenario.

  11. Assessment of model estimates of land-atmosphere CO 2 exchange across Northern Eurasia

    DOE PAGES

    Rawlins, M. A.; McGuire, A. D.; Kimball, J. S.; ...

    2015-07-28

    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 (CO 2) 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 climatemore » model simulations. Model performance benchmarks were drawn from comparisons against both observed CO 2 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 CO 2 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 CO 2 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

  12. High-quality laser cutting of stainless steel in inert gas atmosphere by ytterbium fibre and CO{sub 2} lasers

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Golyshev, A A; Malikov, A G; Orishich, A M

    Processes of cutting stainless steel by ytterbium fibre and CO{sub 2} lasers have been experimentally compared. The cut surface roughnesses for 3- and 5-mm-thick stainless steel sheets are determined. The absorption coefficient of laser radiation during cutting is measured. It is established that the power absorbed by metal during cutting by the CO{sub 2} laser exceeds that for the ytterbium laser (provided that the cutting speed remains the same). The fact that the maximum cutting speed of the CO{sub 2} laser is lower than that of the ytterbium fibre laser is explained. (laser technologies)

  13. Modelling global CO2 emissions into the atmosphere from crown, ground, and peat fires

    NASA Astrophysics Data System (ADS)

    Eliseev, Alexey V.; Mokhov, Igor I.; Chernokulsky, Alexander V.

    2015-04-01

    The scheme for natural fires implemented in the climate model (CM) developed at the A.M. Obukhov Institute of Atmospheric Physics (IAP RAS) is extended by a module accounting for ground and peat fires. With the IAP RAS CM, the simulations are performed for 1700-2300 in accordance with the CMIP5 (Coupled Models Intercomparison Project, phase 5) protocol. The modelled present-day burnt area, BA, and the corresponding CO2 emissions into the atmosphere E agree with the GFED-3.1 estimates at most regions. In the 21st century, under the RCP (Representative Concentration Pathways) scenarios, the global BA increases by 10-41% depending on scenario, and E increases by 11-39%. Under the mitigation scenario RCP 2.6, both BA and E slightly decrease in the 22nd-23rd centuries. For scenarios RCP 4.5, RCP 6.0, and RCP 8.5, they continue to increase in these two centuries. All these changes are mostly due to changes in natural fires activity in the boreal regions. Ground and peat fires contribute significantly to the total emissions of CO2 from natural fires (20-25% at the global scale depending on scenario and calendar year). Peat fires markedly intensify interannual variability of regional CO2 emissions from natural fires.

  14. Particle Size of CO2 Condensates in Mars Atmosphere Revealed by Climate Sounder and Laser Ranging Observations

    NASA Astrophysics Data System (ADS)

    Hu, Renyu

    Current-generation Mars Climate Sounder (MCS) onboard the Mars Reconnaissance Orbiter (MRO) offers extensive coverage of the latitudinal and seasonal distribution of CO_2 condensation in Mars’s atmosphere. The atmospheric temperature profiles measured by MCS reveal that the thickness of CO_2 condensation layer reaches a maximum of 10-15 km (north) or ˜20 km (south) during the middle of winter. There is a shrinking of the CO_2 condensation layer from L_S ˜270(°) to ˜300(°) in 2007, probably related to a planet-encircling dust storm. We integrate the condensation area and the condensation occurrence rate synthesized from the MCS observations to estimate cumulative masses of CO2 condensates deposited onto the northern and southern seasonal polar caps. The mass loading of CO_2 condensate particles, when condensation occurs, can be independently inferred from the detections of reflective clouds by the Mars Orbiter Laser Altimetry (MOLA) onboard the Mars Global Surveyor (MGS). Therefore, we approximate the precipitation flux by the particle settling flux, which is estimated using the impulse responses of MOLA filter channels. With our approach, the total atmospheric condensation mass can be estimated from these observational data sets, with average particle size as the only free parameter. By comparison with the seasonal polar cap masses inferred from the time-varying gravity of Mars, our estimates indicate that the average condensate particle radius is 8 - 22 mum in the northern hemisphere and 4 - 13 mum in the southern hemisphere. This multi-instrument data analysis provides new constraints on modeling the microphysics of CO_2 clouds on Mars.

  15. Microbial imprint on soil-atmosphere H2, COS, and CO2 fluxes

    NASA Astrophysics Data System (ADS)

    Meredith, L. K.; Commane, R.; Munger, J. W.; Wofsy, S. C.; Prinn, R. G.

    2013-12-01

    Microorganisms drive large trace gas fluxes between soil and atmosphere, but the signal can be difficult to detect and quantify in the presence of stronger exchange processes in an ecosystem. Partitioning methods are often needed to estimate trace gas budgets and to develop process-based models to explore the sensitivity of microbe-mediated fluxes. In this study, we test the performance of trace gases with predominantly microbe-mediated soil fluxes as a metric of the soil microbial uptake activity of other trace gases. Using simultaneous, collocated measurements at Harvard Forest, we consider three trace gases with microbe-mediated soil fluxes of various importance relative to their other (mainly plant-mediated) ecosystem fluxes: molecular hydrogen (H2), carbonyl sulfide (COS), and carbon dioxide (CO2). These gases probe different aspects of the soil trace-gas microbiology. Soil H2 uptake is a redox reaction driving the energy metabolism of a portion of the microbial community, while soil CO2 respiration is a partial proxy for the overall soil microbial metabolism. In comparison, very little is understood about the microbiological and environmental drivers of soil COS uptake and emissions. In this study, we find that H2, COS, and CO2 soil uptake rates are often correlated, but the relative soil uptake between gases is not constant, and is influenced by seasonality and local environmental conditions. We also consider how differences in the microbial communities and pathways involved in the soil fluxes may explain differences in the observations. Our results are important for informing previous studies using tracer approaches. For example, H2 has been used to estimate COS soil uptake, which must be accounted for to use COS as a carbon cycle tracer. Furthermore, the global distribution of H2 deposition velocity has been inferred from net primary productivity (CO2). Given that insufficient measurement frequency and spatial distribution exists to partition global net

  16. Method and apparatus for simulating atmospheric absorption of solar energy due to water vapor and CO{sub 2}

    DOEpatents

    Sopori, B.L.

    1995-06-20

    A method and apparatus for improving the accuracy of the simulation of sunlight reaching the earth`s surface includes a relatively small heated chamber having an optical inlet and an optical outlet, the chamber having a cavity that can be filled with a heated stream of CO{sub 2} and water vapor. A simulated beam comprising infrared and near infrared light can be directed through the chamber cavity containing the CO{sub 2} and water vapor, whereby the spectral characteristics of the beam are altered so that the output beam from the chamber contains wavelength bands that accurately replicate atmospheric absorption of solar energy due to atmospheric CO{sub 2} and moisture. 8 figs.

  17. Modeling long-term carbon residue in the ocean-atmosphere system following large CO2 emissions

    NASA Astrophysics Data System (ADS)

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

    2013-12-01

    We use the LOSCAR carbon cycle model (Zeebe et al., 2009; Zeebe, 2012) to calculate the residual carbon in the ocean and atmosphere following large CO2 emissions. We consider the system response to CO2 emissions ranging from 100 to 20000 PgC, and emission durations from 100 yr to 100 kyr, subject to a wide range of system parameters such as the strengths of silicate weathering and the oceanic biological carbon pump. We define the carbon gain factor as the ratio of residual carbon in the ocean-atmosphere to the total emitted carbon. For moderate sized emissions shorter than about 50 kyr, we find that the carbon gain factor grows during the emission and peaks at about 1.7, primarily due to the erosion of carbonate marine sediments. In contrast, for longer emissions, the carbon gain factor peaks at a smaller value, and for very large emissions (more than 5000 PgC), the gain factor decreases with emission size due to carbonate sediment exhaustion. This gain factor is sensitive to model parameters such as low latitude efficiency of the biological pump. The timescale for removal of the residual carbon (reducing the carbon gain factor to zero) depends strongly on the assumed sensitivity of silicate weathering to atmospheric pCO2, and ranges from less than one million years to several million years.

  18. Dynamics of air-sea CO2 fluxes based on FerryBox measurements and satellite-based prediction of pCO2 in the Western English Channel

    NASA Astrophysics Data System (ADS)

    Marrec, Pierre; Thierry, Cariou; Eric, Mace; Pascal, Morin; Marc, Vernet; Yann, Bozec

    2014-05-01

    Since April 2012, we installed an autonomous FerryBox system on a Voluntary Observing Ship (VOS), which crosses the Western English Channel (WEC) between Roscoff and Plymouth on a daily basis. High-frequency data of sea surface temperature (SST), salinity (SSS), fluorescence, dissolved oxygen (DO) and partial pressure of CO2 (pCO2) were recorded for two years across the all-year mixed southern WEC (sWEC) and the seasonally stratified northern WEC (nWEC). These contrasting hydrographical provinces strongly influenced the spatio-temporal distributions of pCO2 and air-sea CO2 fluxes. During the productive period (from May to September), the nWEC acted as a sink for atmospheric CO2 of -5.6 mmolC m-2 d-1 and -4.6 mmolC m-2 d-1, in 2012 and 2013, respectively. During the same period, the sWEC showed significant inter-annual variability degassing CO2 to the atmosphere in 2012 (1.4 mmolC m-2 d-1) and absorbing atmospheric CO2 in 2013 (-1.6 mmolC m-2 d-1). In 2012, high-frequency data revealed that an intense and short (less than 10 days) summer phytoplankton bloom in the nWEC contributed to 31% of the total CO2 drawdown during the productive period, highlighting the necessity of pCO2 high-frequency measurements in coastal ecosystems. Based on this multi-annual dataset, we developed pCO2 algorithms using multiple linear regression (MLR) based on SST, SSS, chlorophyll-a (Chl-a) concentration, time, latitude and mixed layer depth to predict pCO2 in the two hydrographical provinces of the WEC. MLR were performed based on more than 200,000 underway observations spanning the range from 150 to 480 µatm. The root mean square errors (RMSE) of the MLR fit to the data were 17.2 µatm and 21.5 µatm for the s WEC and the nWEC with correlation coefficient (r²) of 0.71 and 0.79, respectively. We applied these algorithms to satellite SST and Chl-a products and to modeled SSS estimates in the entire WEC. Based on these high-frequency and satellite approaches, we will discuss the main

  19. Does phloem loading strategy and capacity alter plant response to elevated atmospheric [CO2]?

    USDA-ARS?s Scientific Manuscript database

    A better understanding of the interactions between photosynthesis, photoassimilate translocation and sink activity is necessary to improve crop productivity. Rising atmospheric [CO2] perturbs source-sink balance which needs to be addressed to adapt crops to future growing conditions. This project ta...

  20. Flux to the atmosphere of CH4 and CO2 from wetland ponds on the Hudson Bay lowlands (HBLs)

    NASA Technical Reports Server (NTRS)

    Hamilton, J. David; Kelly, Carol A.; Rudd, John W. M.; Hesslein, Raymond H.; Roulet, Nigel T.

    1994-01-01

    Ponds on peatlands of the Hudson Bay lowlands (HBLs) are complex ecosystems in which the fluxes to the atmosphere of CH4 and CO2 were controlled by interacting physical and biological factors. This resulted in strong diel variations of both dissolved gas concentrations and gas fluxes to the atmosphere, necessitating frequent sampling on a 24-hour schedule to enable accurate estimates of daily fluxes. Ponds at three sites on the HBL were constant net sources of CH4 and CO2 to the atmosphere at mean rates of 110-180 mg CH4 m(exp -2)/d and 3700-11,000 mg CO2 m(exp -2)/d. Rates peaked in August and September. For CH4 the pond fluxes were 3-30 times higher than adjacent vegetated surfaces. For CO2 the net pond fluxes were similar in magnitude to the vegetated fluxes but the direction of the flux was opposite, toward atmosphere. Even though ponds cover only 8-12% of the HBL area, they accounted for 30% of its total CH4 flux to the atmosphere. There is some circumstantial evidence that the ponds are being formed by decomposition of the underlying peat and that this decomposition is being stimulated by the activity of N2 fixing cyanobacteria that grow in mats at the peat-water interface. The fact that the gas fluxes from the ponds were so different from the surrounding vegetated surfaces means that any change in the ratio of pond to vegetated area, as may occur in response to climate change, would affect the total HBL fluxes.

  1. Detection of CO and HCN in Pluto's atmosphere with ALMA

    NASA Astrophysics Data System (ADS)

    Lellouch, E.; Gurwell, M.; Butler, B.; Fouchet, T.; Lavvas, P.; Strobel, D. F.; Sicardy, B.; Moullet, A.; Moreno, R.; Bockelée-Morvan, D.; Biver, N.; Young, L.; Lis, D.; Stansberry, J.; Stern, A.; Weaver, H.; Young, E.; Zhu, X.; Boissier, J.

    2017-04-01

    Observations of the Pluto-Charon system, acquired with the ALMA interferometer on June 12-13, 2015, have led to the detection of the CO(3-2) and HCN(4-3) rotational transitions from Pluto (including the hyperfine structure of HCN), providing a strong confirmation of the presence of CO, and the first observation of HCN in Pluto's atmosphere. The CO and HCN lines probe Pluto's atmosphere up to ∼450 km and ∼900 km altitude, respectively, with a large contribution due to limb emission. The CO detection yields (i) a much improved determination of the CO mole fraction, as 515 ± 40 ppm for a 12 μbar surface pressure (ii) strong constraints on Pluto's mean atmospheric dayside temperature profile over ∼50-400 km, with clear evidence for a well-marked temperature decrease (i.e., mesosphere) above the 30-50 km stratopause and a best-determined temperature of 70 ± 2 K at 300 km, somewhat lower than previously estimated from stellar occultations (81 ± 6 K), and in agreement with recent inferences from New Horizons / Alice solar occultation data. The HCN line shape implies a high abundance of this species in the upper atmosphere, with a mole fraction >1.5 × 10-5 above 450 km and a value of 4 × 10-5 near 800 km. Assuming HCN at saturation, this would require a warm (>92 K) upper atmosphere layer; while this is not ruled out by the CO emission, it is inconsistent with the Alice-measured CH4 and N2 line-of-sight column densities. Taken together, the large HCN abundance and the cold upper atmosphere imply supersaturation of HCN to a degree (7-8 orders of magnitude) hitherto unseen in planetary atmospheres, probably due to a lack of condensation nuclei above the haze region and the slow kinetics of condensation at the low pressure and temperature conditions of Pluto's upper atmosphere. HCN is also present in the bottom ∼100 km of the atmosphere, with a 10-8-10-7 mole fraction; this implies either HCN saturation or undersaturation there, depending on the precise

  2. Detection of Atmospheric CO on Pluto with ALMA

    NASA Astrophysics Data System (ADS)

    Gurwell, Mark; Lellouch, Emmanuel; Butler, Bryan; Moullet, Arielle; Moreno, Raphael; Bockelée-Morvan, Dominique; Biver, Nicolas; Fouchet, Thierry; Lis, Darek; Stern, Alan; Young, Leslie; Young, Eliot; Weaver, Hal; Boissier, Jeremie; Stansberry, John

    2015-11-01

    We observed Pluto and Charon using the Atacama Large Millimeter/submillimeter Array (ALMA) interferometer in Northern Chile on June 12.2 and June 13.15, 2015, just one month prior to the New Horizons flyby of the system. The configuration of ALMA at the time provided ~0.3" resolution, allowing separation of emission from Pluto and Charon. This project targeted multiple science goals, including a search for HCN in Pluto's atmosphere [1] and high precision measurements of the individual brightness temperatures of Pluto and Charon [2], also presented at this meeting. Here we report the high SNR detection of carbon monoxide in the atmosphere of Pluto. The CO(3-2) rotational line, at 345.796 GHz (867 μm), was observed with 117 kHz spectral resolution for 45 min (on-source) on each date, providing ~3.5mJy/channel RMS. CO emission was clearly detected on both days, with a contrast of ~65 mJy above the Pluto continuum, and ~1.8 MHz FWHM linewidth, with the combined integrated line SNR >50. The presence of CO in Pluto's atmosphere is expected due to it's presence as ice on the surface in vapor pressure equilibrium with the atmosphere (e.g. [3],[4]), and it was previously detected at modest SNR in the near-IR using the VLT [5]. A preliminary assessment based upon the CO line wings shows the fractional abundance of CO is 500-750 ppm, consistent with that found in [5]. Further, the shape of the line core emission (assuming a constant CO mixing ratio), suggests that the atmospheric temperature rises quickly from the surface to ~100-110 K in the altitude range 20-70 km but decreases above that, falling to about 70 K by 200 km altitude. A detailed line inversion analysis will be performed and results presented.[1] Lellouch et al, this meeting. [2] Butler et al., this meeting. [3] Owen et al (1993), Science, 261, pp. 745-748. [4] Spencer et al (1993), In Pluto and Charon, pp. 435-473. Univ. of Arizona Press, Tucson. [5] Lellouch et al (2011), A&A, 530, L4.

  3. Effect of elevated atmospheric CO2 concentration on growth and leaf litter decomposition of Quercus acutissima and Fraxinus rhynchophylla

    PubMed Central

    Cha, Sangsub; Chae, Hee-Myung; Lee, Sang-Hoon; Shim, Jae-Kuk

    2017-01-01

    The atmospheric carbon dioxide (CO2) level is expected to increase substantially, which may change the global climate and carbon dynamics in ecosystems. We examined the effects of an elevated atmospheric CO2 level on the growth of Quercus acutissima and Fraxinus rhynchophylla seedlings. We investigated changes in the chemical composition of leaf litter, as well as litter decomposition. Q. acutissima and F. rhynchophylla did not show differences in dry weight between ambient CO2 and enriched CO2 treatments, but they exhibited different patterns of carbon allocation, namely, lower shoot/root ratio (S/R) and decreased specific leaf area (SLA) under CO2-enriched conditions. The elevated CO2 concentration significantly reduced the nitrogen concentration in leaf litter while increasing lignin concentrations and carbon/nitrogen (C/N) and lignin/N ratios. The microbial biomass associated with decomposing Q. acutissima leaf litter was suppressed in CO2 enrichment chambers, while that of F. rhynchophylla was not. The leaf litter of Q. acutissima from the CO2-enriched chambers, in contrast with F. rhynchophylla, contained much lower nutrient concentrations than that of the litter in the ambient air chambers. Consequently, poorer litter quality suppressed decomposition. PMID:28182638

  4. Effect of elevated atmospheric CO2 concentration on growth and leaf litter decomposition of Quercus acutissima and Fraxinus rhynchophylla.

    PubMed

    Cha, Sangsub; Chae, Hee-Myung; Lee, Sang-Hoon; Shim, Jae-Kuk

    2017-01-01

    The atmospheric carbon dioxide (CO2) level is expected to increase substantially, which may change the global climate and carbon dynamics in ecosystems. We examined the effects of an elevated atmospheric CO2 level on the growth of Quercus acutissima and Fraxinus rhynchophylla seedlings. We investigated changes in the chemical composition of leaf litter, as well as litter decomposition. Q. acutissima and F. rhynchophylla did not show differences in dry weight between ambient CO2 and enriched CO2 treatments, but they exhibited different patterns of carbon allocation, namely, lower shoot/root ratio (S/R) and decreased specific leaf area (SLA) under CO2-enriched conditions. The elevated CO2 concentration significantly reduced the nitrogen concentration in leaf litter while increasing lignin concentrations and carbon/nitrogen (C/N) and lignin/N ratios. The microbial biomass associated with decomposing Q. acutissima leaf litter was suppressed in CO2 enrichment chambers, while that of F. rhynchophylla was not. The leaf litter of Q. acutissima from the CO2-enriched chambers, in contrast with F. rhynchophylla, contained much lower nutrient concentrations than that of the litter in the ambient air chambers. Consequently, poorer litter quality suppressed decomposition.

  5. Southern Ocean acidification: A tipping point at 450-ppm atmospheric CO2

    PubMed Central

    McNeil, Ben I.; Matear, Richard J.

    2008-01-01

    Southern Ocean acidification via anthropogenic CO2 uptake is expected to be detrimental to multiple calcifying plankton species by lowering the concentration of carbonate ion (CO32−) to levels where calcium carbonate (both aragonite and calcite) shells begin to dissolve. Natural seasonal variations in carbonate ion concentrations could either hasten or dampen the future onset of this undersaturation of calcium carbonate. We present a large-scale Southern Ocean observational analysis that examines the seasonal magnitude and variability of CO32− and pH. Our analysis shows an intense wintertime minimum in CO32− south of the Antarctic Polar Front and when combined with anthropogenic CO2 uptake is likely to induce aragonite undersaturation when atmospheric CO2 levels reach ≈450 ppm. Under the IPCC IS92a scenario, Southern Ocean wintertime aragonite undersaturation is projected to occur by the year 2030 and no later than 2038. Some prominent calcifying plankton, in particular the Pteropod species Limacina helicina, have important veliger larval development during winter and will have to experience detrimental carbonate conditions much earlier than previously thought, with possible deleterious flow-on impacts for the wider Southern Ocean marine ecosystem. Our results highlight the critical importance of understanding seasonal carbon dynamics within all calcifying marine ecosystems such as continental shelves and coral reefs, because natural variability may potentially hasten the onset of future ocean acidification. PMID:19022908

  6. Effects of high CO2 levels on surface temperature and atmospheric oxidation state of the early earth

    NASA Technical Reports Server (NTRS)

    Kasting, J. F.; Pollack, J. B.; Crisp, D.

    1984-01-01

    One-dimensional radiative and photochemical models are used to determine how much CO2 must have been present to maintain a temperate early climate and to examine the consequences that are implied for the controls on atmospheric oxidation state. It is shown that CO2 concentrations of the order of 1000 PAL are required to keep the average surface temperature close to the present value, if albedo changes and heating by reduced greenhouse gases were relatively unimportant. The oxidation state of such a high-CO2, prebiotic atmosphere should have been largely determined by the balance between the H2O2 rainout rate and the rate at which hydrogen escaped to space, with only a weak dependence on the volcanic outgassing rate or on other speculative sources of H2. The implied upper limit on the ground-level O2 mixing ratio is approximately 10 to the -11th and is subject to less uncertainty than the results of previous models.

  7. Phosphorus feedbacks constraining tropical ecosystem responses to changes in atmospheric CO 2 and climate

    DOE PAGES

    Yang, Xiaojuan; Thornton, Peter E.; Ricciuto, Daniel M.; ...

    2016-07-14

    The effects of phosphorus (P) availability on carbon (C) cycling in the Amazon region are investigated using CLM-CNP. Within this paper, we demonstrate that the coupling of P dynamics reduces the simulated historical terrestrial C sink due to increasing atmospheric CO 2 concentrations ([CO 2]) by about 26%. Our exploratory simulations show that the response of tropical forest C cycling to increasing [CO 2] depends on how elevated CO 2 affects phosphatase enzyme production. The effects of warming are more complex, depending on the interactions between humidity, C, and nutrient dynamics. While a simulation with low humidity generally shows themore » reduction of net primary productivity (NPP), a second simulation with higher humidity suggests overall increases in NPP due to the dominant effects of reduced water stress and more nutrient availability. Lastly, our simulations point to the need for (1) new observations on how elevated [CO 2] affects phosphatase enzyme production and (2) more tropical leaf-scale measurements under different temperature/humidity conditions with different soil P availability.« less

  8. Using Mauna Loa Atmospheric CO2 Data in Large General Education Geoscience Courses

    NASA Astrophysics Data System (ADS)

    Richardson, R. M.; Kapp, J. L.

    2007-12-01

    We have been using the Mauna Loa atmospheric CO2 dataset (http://scrippsco2.ucsd.edu/data/in_situ_co2/monthly_mlo.csv) in a large (up to 300) General Education Geoscience course, primarily in small breakout groups (30 students). The exercise is designed to address quantitative literacy including percentages, slopes and linear trends, issues of data completeness and bias, quality of extrapolations, as well as implications for climate change. We are significantly revising the course, which serves 600 students a semester, with help from a curriculum grant. A major goal is to improve student learning by incorporating inquiry based activities in the large lecture setting. Lectures now incorporate several activities throughout a given class period, in which students are asked to use critical thinking skills such as interpreting patterns in data and graphs, analyzing a scientific hypothesis for its coherence with the scientific method, and answering higher order synthesis questions in both verbal and written form. This differs from our past format where class periods were dominated by lecture, with a single short activity done individually about every other lecture. To test the effectiveness of the new course format we will give students the same atmospheric CO2 exercise in the lecture setting that they were given previously in breakout groups. Students will work in small groups in lecture after receiving a short introduction to the exercise by the instructor. They will plot CO2 concentrations, make extrapolations, and interpret patterns in the data. We will compare scores on the exercise with previous semesters. We expect that students will do better having had more experience with interpreting scientific data and practicing higher order thinking skills. We also expect working in small groups will foster better learning through peer teaching and discussion. We will incorporate responses from students who took part in the exercises from current and previous semesters. We

  9. Contribution of various carbon sources toward isoprene biosynthesis in poplar leaves mediated by altered atmospheric CO2 concentrations.

    PubMed

    Trowbridge, Amy M; Asensio, Dolores; Eller, Allyson S D; Way, Danielle A; Wilkinson, Michael J; Schnitzler, Jörg-Peter; Jackson, Robert B; Monson, Russell K

    2012-01-01

    Biogenically released isoprene plays important roles in both tropospheric photochemistry and plant metabolism. We performed a (13)CO(2)-labeling study using proton-transfer-reaction mass spectrometry (PTR-MS) to examine the kinetics of recently assimilated photosynthate into isoprene emitted from poplar (Populus × canescens) trees grown and measured at different atmospheric CO(2) concentrations. This is the first study to explicitly consider the effects of altered atmospheric CO(2) concentration on carbon partitioning to isoprene biosynthesis. We studied changes in the proportion of labeled carbon as a function of time in two mass fragments, M41(+), which represents, in part, substrate derived from pyruvate, and M69(+), which represents the whole unlabeled isoprene molecule. We observed a trend of slower (13)C incorporation into isoprene carbon derived from pyruvate, consistent with the previously hypothesized origin of chloroplastic pyruvate from cytosolic phosphenolpyruvate (PEP). Trees grown under sub-ambient CO(2) (190 ppmv) had rates of isoprene emission and rates of labeling of M41(+) and M69(+) that were nearly twice those observed in trees grown under elevated CO(2) (590 ppmv). However, they also demonstrated the lowest proportion of completely labeled isoprene molecules. These results suggest that under reduced atmospheric CO(2) availability, more carbon from stored/older carbon sources is involved in isoprene biosynthesis, and this carbon most likely enters the isoprene biosynthesis pathway through the pyruvate substrate. We offer direct evidence that extra-chloroplastic rather than chloroplastic carbon sources are mobilized to increase the availability of pyruvate required to up-regulate the isoprene biosynthesis pathway when trees are grown under sub-ambient CO(2).

  10. Contribution of Various Carbon Sources Toward Isoprene Biosynthesis in Poplar Leaves Mediated by Altered Atmospheric CO2 Concentrations

    PubMed Central

    Trowbridge, Amy M.; Asensio, Dolores; Eller, Allyson S. D.; Way, Danielle A.; Wilkinson, Michael J.; Schnitzler, Jörg-Peter; Jackson, Robert B.; Monson, Russell K.

    2012-01-01

    Biogenically released isoprene plays important roles in both tropospheric photochemistry and plant metabolism. We performed a 13CO2-labeling study using proton-transfer-reaction mass spectrometry (PTR-MS) to examine the kinetics of recently assimilated photosynthate into isoprene emitted from poplar (Populus × canescens) trees grown and measured at different atmospheric CO2 concentrations. This is the first study to explicitly consider the effects of altered atmospheric CO2 concentration on carbon partitioning to isoprene biosynthesis. We studied changes in the proportion of labeled carbon as a function of time in two mass fragments, M41+, which represents, in part, substrate derived from pyruvate, and M69+, which represents the whole unlabeled isoprene molecule. We observed a trend of slower 13C incorporation into isoprene carbon derived from pyruvate, consistent with the previously hypothesized origin of chloroplastic pyruvate from cytosolic phosphenolpyruvate (PEP). Trees grown under sub-ambient CO2 (190 ppmv) had rates of isoprene emission and rates of labeling of M41+ and M69+ that were nearly twice those observed in trees grown under elevated CO2 (590 ppmv). However, they also demonstrated the lowest proportion of completely labeled isoprene molecules. These results suggest that under reduced atmospheric CO2 availability, more carbon from stored/older carbon sources is involved in isoprene biosynthesis, and this carbon most likely enters the isoprene biosynthesis pathway through the pyruvate substrate. We offer direct evidence that extra-chloroplastic rather than chloroplastic carbon sources are mobilized to increase the availability of pyruvate required to up-regulate the isoprene biosynthesis pathway when trees are grown under sub-ambient CO2. PMID:22384238

  11. Influence of Suprathermal Atoms on the Escape and Evolution of Mars' CO2 Atmosphere

    NASA Astrophysics Data System (ADS)

    Lichtenegger, H.; Amerstorfer, U. V.; Gröller, H.; Tian, F.; Lammer, H.; Noack, L.; Johnstone, C.; Tu, L.

    2017-09-01

    Suprathermal oxygen and carbon atoms are produced by photochemical processes in the upper atmosphere of Mars. Due to their relatively high energies, these particle form an extended corona around Mars and can be picked up by the solar wind and emoved from the planet. The influence of an increased EUV flux, as it prevailed in the past, on the formation of the corona is studied and the corresponding loss rates are estimated. It is shown that the atmospheric loss due to the various processes varies with time and that most of the initial CO2 atmosphere is removed within the first few hundred million years after the formation of the planet. These results are important in order to better understand the atmosphere evolution of terrestrial planets.

  12. Mass wasting triggered by seasonal CO2 sublimation under Martian atmospheric conditions: Laboratory experiments

    NASA Astrophysics Data System (ADS)

    Sylvest, Matthew E.; Conway, Susan J.; Patel, Manish R.; Dixon, John C.; Barnes, Adam

    2016-12-01

    Sublimation is a recognized process by which planetary landscapes can be modified. However, interpretation of whether sublimation is involved in downslope movements on Mars and other bodies is restricted by a lack of empirical data to constrain this mechanism of sediment transport and its influence on landform morphology. Here we present the first set of laboratory experiments under Martian atmospheric conditions which demonstrate that the sublimation of CO2 ice from within the sediment body can trigger failure of unconsolidated, regolith slopes and can measurably alter the landscape. Previous theoretical studies required CO2 slab ice for movements, but we find that only frost is required. Hence, sediment transport by CO2 sublimation could be more widely applicable (in space and time) on Mars than previously thought. This supports recent work suggesting CO2 sublimation could be responsible for recent modification in Martian gullies.

  13. Soil type influences the sensitivity of nutrient dynamics to changes in atmospheric CO2

    USDA-ARS?s Scientific Manuscript database

    Numerous studies have indicated that increases in atmospheric CO2 have the potential to decrease nitrogen availability through the process of progressive nitrogen limitation (PNL). The timing and magnitude of PNL in field experiments is varied due to numerous ecosystem processes. Here we examined ...

  14. Soil type influences the sensitivity of nutrient dynamics to changes in atmospheric CO2

    USDA-ARS?s Scientific Manuscript database

    Numerous studies have indicated that increases in atmospheric CO2 have the potential to decrease nitrogen availability through the process of progressive nitrogen limitation (PNL). The timing and magnitude of PNL in field experiments is varied due to numerous ecosystem processes. Here we examined th...

  15. A Database of Herbaceous Vegetation Responses to Elevated Atmospheric CO2 (NDP-073)

    DOE Data Explorer

    Jones, Michael H [The Ohio State Univ., Columbus, OH (United States); Curtis, Peter S [The Ohio State Univ., Columbus, OH (United States); Cushman, Robert M [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Brenkert, Antoinette L [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States)

    1999-01-01

    To perform a statistically rigorous meta-analysis of research results on the response by herbaceous vegetation to increased atmospheric CO2 levels, a multiparameter database of responses was compiled from the published literature. Seventy-eight independent CO2-enrichment studies, covering 53 species and 26 response parameters, reported mean response, sample size, and variance of the response (either as standard deviation or standard error). An additional 43 studies, covering 25 species and 6 response parameters, did not report variances. This numeric data package accompanies the Carbon Dioxide Information Analysis Center's (CDIAC's) NDP- 072, which provides similar information for woody vegetation. This numeric data package contains a 30-field data set of CO2- exposure experiment responses by herbaceous plants (as both a flat ASCII file and a spreadsheet file), files listing the references to the CO2-exposure experiments and specific comments relevant to the data in the data sets, and this documentation file (which includes SAS and Fortran codes to read the ASCII data file; SAS is a registered trademark of the SAS Institute, Inc., Cary, North Carolina 27511).

  16. An Analytical Framework for the Steady State Impact of Carbonate Compensation on Atmospheric CO2

    NASA Astrophysics Data System (ADS)

    Omta, Anne Willem; Ferrari, Raffaele; McGee, David

    2018-04-01

    The deep-ocean carbonate ion concentration impacts the fraction of the marine calcium carbonate production that is buried in sediments. This gives rise to the carbonate compensation feedback, which is thought to restore the deep-ocean carbonate ion concentration on multimillennial timescales. We formulate an analytical framework to investigate the impact of carbonate compensation under various changes in the carbon cycle relevant for anthropogenic change and glacial cycles. Using this framework, we show that carbonate compensation amplifies by 15-20% changes in atmospheric CO2 resulting from a redistribution of carbon between the atmosphere and ocean (e.g., due to changes in temperature, salinity, or nutrient utilization). A counterintuitive result emerges when the impact of organic matter burial in the ocean is examined. The organic matter burial first leads to a slight decrease in atmospheric CO2 and an increase in the deep-ocean carbonate ion concentration. Subsequently, enhanced calcium carbonate burial leads to outgassing of carbon from the ocean to the atmosphere, which is quantified by our framework. Results from simulations with a multibox model including the minor acids and bases important for the ocean-atmosphere exchange of carbon are consistent with our analytical predictions. We discuss the potential role of carbonate compensation in glacial-interglacial cycles as an example of how our theoretical framework may be applied.

  17. Differences in the response sensitivity of stomatal index to atmospheric CO2 among four genera of Cupressaceae conifers.

    PubMed

    Haworth, Matthew; Heath, James; McElwain, Jennifer C

    2010-03-01

    The inverse relationship between stomatal density (SD: number of stomata per mm(2) leaf area) and atmospheric concentration of CO2 ([CO2]) permits the use of plants as proxies of palaeo-atmospheric CO2. Many stomatal reconstructions of palaeo-[CO2] are based upon multiple fossil species. However, it is unclear how plants respond to [CO2] across genus, family or ecotype in terms of SD or stomatal index (SI: ratio of stomata to epidermal cells). This study analysed the stomatal numbers of conifers from the ancient family Cupressaceae, in order to examine the nature of the SI-[CO2] relationship, and potential implications for stomatal reconstructions of palaeo-[CO2]. Methods Stomatal frequency measurements were taken from historical herbarium specimens of Athrotaxis cupressoides, Tetraclinis articulata and four Callitris species, and live A. cupressoides grown under CO2-enrichment (370, 470, 570 and 670 p.p.m. CO2). T. articulata, C. columnaris and C. rhomboidea displayed significant reductions in SI with rising [CO2]; by contrast, A. cupressoides, C. preissii and C. oblonga show no response in SI. However, A. cupressoides does reduce SI to increases in [CO2] above current ambient (approx. 380 p.p.m. CO2). This dataset suggests that a shared consistent SI-[CO2] relationship is not apparent across the genus Callitris. Conclusions The present findings suggest that it is not possible to generalize how conifer species respond to fluctuations in [CO2] based upon taxonomic relatedness or habitat. This apparent lack of a consistent response, in conjunction with high variability in SI, indicates that reconstructions of absolute palaeo-[CO2] based at the genus level, or upon multiple species for discrete intervals of time are not as reliable as those based on a single or multiple temporally overlapping species.

  18. Differences in the response sensitivity of stomatal index to atmospheric CO2 among four genera of Cupressaceae conifers

    PubMed Central

    Haworth, Matthew; Heath, James; McElwain, Jennifer C.

    2010-01-01

    Background and Aims The inverse relationship between stomatal density (SD: number of stomata per mm2 leaf area) and atmospheric concentration of CO2 ([CO2]) permits the use of plants as proxies of palaeo-atmospheric CO2. Many stomatal reconstructions of palaeo-[CO2] are based upon multiple fossil species. However, it is unclear how plants respond to [CO2] across genus, family or ecotype in terms of SD or stomatal index (SI: ratio of stomata to epidermal cells). This study analysed the stomatal numbers of conifers from the ancient family Cupressaceae, in order to examine the nature of the SI–[CO2] relationship, and potential implications for stomatal reconstructions of palaeo-[CO2]. Methods Stomatal frequency measurements were taken from historical herbarium specimens of Athrotaxis cupressoides, Tetraclinis articulata and four Callitris species, and live A. cupressoides grown under CO2-enrichment (370, 470, 570 and 670 p.p.m. CO2). Key Results T. articulata, C. columnaris and C. rhomboidea displayed significant reductions in SI with rising [CO2]; by contrast, A. cupressoides, C. preissii and C. oblonga show no response in SI. However, A. cupressoides does reduce SI to increases in [CO2] above current ambient (approx. 380 p.p.m. CO2). This dataset suggests that a shared consistent SI–[CO2] relationship is not apparent across the genus Callitris. Conclusions The present findings suggest that it is not possible to generalize how conifer species respond to fluctuations in [CO2] based upon taxonomic relatedness or habitat. This apparent lack of a consistent response, in conjunction with high variability in SI, indicates that reconstructions of absolute palaeo-[CO2] based at the genus level, or upon multiple species for discrete intervals of time are not as reliable as those based on a single or multiple temporally overlapping species. PMID:20089556

  19. The influence of continental ice, atmospheric CO2, and land albedo on the climate of the last glacial maximum

    NASA Astrophysics Data System (ADS)

    Broccoli, A. J.; Manabe, S.

    1987-02-01

    The contributions of expanded continental ice, reduced atmospheric CO2, and changes in land albedo to the maintenance of the climate of the last glacial maximum (LGM) are examined. A series of experiments is performed using an atmosphere-mixed layer ocean model in which these changes in boundary conditions are incorporated either singly or in combination. The model used has been shown to produce a reasonably realistic simulation of the reduced temperature of the LGM (Manabe and Broccoli 1985b). By comparing the results from pairs of experiments, the effects of each of these environmental changes can be determined. Expanded continental ice and reduced atmospheric CO2 are found to have a substantial impact on global mean temperature. The ice sheet effect is confined almost exclusively to the Northern Hemisphere, while lowered CO2 cools both hemispheres. Changes in land albedo over ice-free areas have only a minor thermal effect on a global basis. The reduction of CO2 content in the atmosphere is the primary contributor to the cooling of the Southern Hemisphere. The model sensitivity to both the ice sheet and CO2 effects is characterized by a high latitude amplification and a late autumn and early winter maximum. Substantial changes in Northern Hemisphere tropospheric circulation are found in response to LGM boundary conditions during winter. An amplified flow pattern and enhanced westerlies occur in the vicinity of the North American and Eurasian ice sheets. These alterations of the tropospheric circulation are primarily the result of the ice sheet effect, with reduced CO2 contributing only a slight amplification of the ice sheet-induced pattern.

  20. Quantifying the impact of El Niño-driven variations in temperature and precipitation on regional atmospheric CO2 growth rate variations

    NASA Astrophysics Data System (ADS)

    Keppel-Aleks, G.; Butterfield, Z.; Doney, S. C.; Dlugokencky, E. J.; Miller, J.; Morton, D. C.

    2017-12-01

    Quantifying the climatic drivers of variations in atmospheric CO2 observations over a range of timescales is necessary to develop a mechanistic understanding of the global carbon cycle that will enable prediction of future changes. Here, we combine NOAA cooperative global air sampling network CO2 observations, remote sensing data, and a flux perturbation model to quantify the feedbacks between interannual variability in physical climate and the atmospheric CO2 growth rate. In particular, we focus on the differences between the 1997/1998 El Niño and the 2015/2016 El Niño during which atmospheric CO2 increased at an unprecedented rate. The flux perturbation model was trained on data from 1997 to 2012, and then used to predict regional atmospheric CO2 growth rate anomalies for the period from 2013 through 2016. Given gridded temperature anomalies from the Hadley Center's Climate Research Unit (CRU), precipitation anomalies from the Global Precipitation Climatology Project (GPCP), and fire emissions from the Global Fire Emissions Database (GFEDv4s), the model was able to the reproduce regional growth rate variations observed at marine boundary layer stations in the NOAA network, including the rapid CO2 growth rate in 2015/2016. The flux perturbation model output suggests that the carbon cycle responses differed for1997 and 2015 El Niño periods, with tropical precipitation anomalies causing a much larger net flux of CO2 to the atmosphere during the latter period, while direct fire emissions dominated the former. The flux perturbation model also suggests that high temperature stress in the Northern Hemisphere extratropics contributed almost one-third of the CO2 growth rate enhancement during the 2015 El Niño. We use satellite-based metrics for atmospheric column CO2, vegetation, and moisture to corroborate the regional El Niño impacts from the flux perturbation model. Finally, we discuss how these observational results and independent data on ocean air-sea flux

  1. Mechanism of matrix-bound phosphine production in response to atmospheric elevated CO2 in paddy soils.

    PubMed

    An, Shaorong; Niu, Xiaojun; Chen, Weiyi; Sheng, Hong; Lai, Senchao; Yang, Zhiquan; Gu, Xiaohong; Zhou, Shaoqi

    2018-04-12

    To explore the effect of elevated CO 2 concentrations ([CO 2 ]) on phosphine formation in paddy fields, the matrix-bound phosphine (MBP) content, different phosphorus fractions and various carbon forms in soil samples from rice cultivation under varying CO 2 concentrations of 400 ppm, 550 ppm and 700 ppm by indoor simulation experiment were determined. This study showed that MBP concentration did not increase significantly with elevated [CO 2 ] over four-week cultivation periods of rice seedlings, regardless of soil layers. MBP had a significant positive correlation with total phosphorus (TP) and inorganic phosphorus (IP), and multiple stepwise linear regression analysis further indicated that MBP preservation in neutral paddy soils with depths of 0-20 cm may have been due to conversion from FeP and CaP. Based on redundancy analysis and forward selection analysis, speculated that the formation of MBP in the neutral paddy soils as the response to atmospheric elevated [CO 2 ] was due to two processes: (i) FeP transformation affected by the changes of soil respiration (SCO 2 ) and TOC was the main precursor for the production of MBP; and (ii) CaP transformation resulting from variation in HCO 3 - was the secondary MBP source. The complex combination of these two processes is simultaneously controlled by SCO 2 . In a word, the soil environment in the condition of elevated [CO 2 ] was in favor of MBP storage in neutral paddy soils. The results of our study imply that atmospheric CO 2 participates in and has a certain impact on the global biogeochemical cycle of phosphorus. Copyright © 2018 Elsevier Ltd. All rights reserved.

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

    NASA Astrophysics Data System (ADS)

    Lac, C.; Donnelly, R. P.; Masson, V.; Pal, S.; Riette, S.; Donier, S.; Queguiner, S.; Tanguy, G.; Ammoura, L.; Xueref-Remy, I.

    2013-05-01

    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 sensitivity test without

  3. Constraints on Southern Ocean CO2 Fluxes and Seasonality from Atmospheric Vertical Gradients Observed on Multiple Airborne Campaigns

    NASA Astrophysics Data System (ADS)

    McKain, K.; Sweeney, C.; Stephens, B. B.; Long, M. C.; Jacobson, A. R.; Basu, S.; Chatterjee, A.; Weir, B.; Wofsy, S. C.; Atlas, E. L.; Blake, D. R.; Montzka, S. A.; Stern, R.

    2017-12-01

    The Southern Ocean plays an important role in the global carbon cycle and climate system, but net CO2 flux into the Southern Ocean is difficult to measure and model because it results from large opposing and seasonally-varying fluxes due to thermal forcing, biological uptake, and deep-water mixing. We present an analysis to constrain the seasonal cycle of net CO2 exchange with the Southern Ocean, and the magnitude of summer uptake, using the vertical gradients in atmospheric CO2 observed during three aircraft campaigns in the southern polar region. The O2/N2 Ratio and CO2 Airborne Southern Ocean Study (ORCAS) was an airborne campaign that intensively sampled the atmosphere at 0-13 km altitude and 45-75 degrees south latitude in the austral summer (January-February) of 2016. The global airborne campaigns, the HIAPER Pole-to-Pole Observations (HIPPO) study and the Atmospheric Tomography Mission (ATom), provide additional measurements over the Southern Ocean from other seasons and multiple years (2009-2011, 2016-2017). Derivation of fluxes from measured vertical gradients requires robust estimates of the residence time of air in the polar tropospheric domain, and of the contribution of long-range transport from northern latitudes outside the domain to the CO2 gradient. We use diverse independent approaches to estimate both terms, including simulations using multiple transport and flux models, and observed gradients of shorter-lived tracers with specific sources regions and well-known loss processes. This study demonstrates the utility of aircraft profile measurements for constraining large-scale air-sea fluxes for the Southern Ocean, in contrast to those derived from the extrapolation of sparse ocean and atmospheric measurements and uncertain flux parameterizations.

  4. CUVE - Cubesat UV Experiment: Unveil Venus' UV Absorber with Cubesat UV Mapping Spectrometer

    NASA Astrophysics Data System (ADS)

    Cottini, V.; Aslam, S.; D'Aversa, E.; Glaze, L.; Gorius, N.; Hewagama, T.; Ignatiev, N.; Piccioni, G.

    2017-09-01

    Our Venus mission concept Cubesat UV Experiment (CUVE) is one of ten proposals selected for funding by the NASA PSDS3 Program - Planetary Science Deep Space SmallSat Studies. CUVE concept is to insert a CubeSat spacecraft into a Venusian orbit and perform remote sensing of the UV spectral region using a high spectral resolution point spectrometer to resolve UV molecular bands, observe nightglow, and characterize the unidentified main UV absorber. The UV spectrometer is complemented by an imaging UV camera with multiple bands in the UV absorber main band range for contextual imaging. CUVE Science Objectives are: the nature of the "Unknown" UV-absorber; the abundances and distributions of SO2 and SO at and above Venus's cloud tops and their correlation with the UV absorber; the atmospheric dynamics at the cloud tops, structure of upper clouds and wind measurements from cloud-tracking; the nightglow emissions: NO, CO, O2. This mission will therefore be an excellent platform to study Venus' cloud top atmospheric properties where the UV absorption drives the planet's energy balance. CUVE would complement past, current and future Venus missions with conventional spacecraft, and address critical science questions cost effectively.

  5. Atmospheric CO2 observations and models suggest strong carbon uptake by forests in New Zealand

    NASA Astrophysics Data System (ADS)

    Steinkamp, Kay; Mikaloff Fletcher, Sara E.; Brailsford, Gordon; Smale, Dan; Moore, Stuart; Keller, Elizabeth D.; Baisden, W. Troy; Mukai, Hitoshi; Stephens, Britton B.

    2017-01-01

    A regional atmospheric inversion method has been developed to determine the spatial and temporal distribution of CO2 sinks and sources across New Zealand for 2011-2013. This approach infers net air-sea and air-land CO2 fluxes from measurement records, using back-trajectory simulations from the Numerical Atmospheric dispersion Modelling Environment (NAME) Lagrangian dispersion model, driven by meteorology from the New Zealand Limited Area Model (NZLAM) weather prediction model. The inversion uses in situ measurements from two fixed sites, Baring Head on the southern tip of New Zealand's North Island (41.408° S, 174.871° E) and Lauder from the central South Island (45.038° S, 169.684° E), and ship board data from monthly cruises between Japan, New Zealand, and Australia. A range of scenarios is used to assess the sensitivity of the inversion method to underlying assumptions and to ensure robustness of the results. The results indicate a strong seasonal cycle in terrestrial land fluxes from the South Island of New Zealand, especially in western regions covered by indigenous forest, suggesting higher photosynthetic and respiratory activity than is evident in the current a priori land process model. On the annual scale, the terrestrial biosphere in New Zealand is estimated to be a net CO2 sink, removing 98 (±37) Tg CO2 yr-1 from the atmosphere on average during 2011-2013. This sink is much larger than the reported 27 Tg CO2 yr-1 from the national inventory for the same time period. The difference can be partially reconciled when factors related to forest and agricultural management and exports, fossil fuel emission estimates, hydrologic fluxes, and soil carbon change are considered, but some differences are likely to remain. Baseline uncertainty, model transport uncertainty, and limited sensitivity to the northern half of the North Island are the main contributors to flux uncertainty.

  6. Plant-soil distribution of potentially toxic elements in response to elevated atmospheric CO2.

    PubMed

    Duval, Benjamin D; Dijkstra, Paul; Natali, Susan M; Megonigal, J Patrick; Ketterer, Michael E; Drake, Bert G; Lerdau, Manuel T; Gordon, Gwyneth; Anbar, Ariel D; Hungate, Bruce A

    2011-04-01

    The distribution of contaminant elements within ecosystems is an environmental concern because of these elements' potential toxicity to animals and plants and their ability to hinder microbial ecosystem services. As with nutrients, contaminants are cycled within and through ecosystems. Elevated atmospheric CO2 generally increases plant productivity and alters nutrient element cycling, but whether CO2 causes similar effects on the cycling of contaminant elements is unknown. Here we show that 11 years of experimental CO2 enrichment in a sandy soil with low organic matter content causes plants to accumulate contaminants in plant biomass, with declines in the extractable contaminant element pools in surface soils. These results indicate that CO2 alters the distribution of contaminant elements in ecosystems, with plant element accumulation and declining soil availability both likely explained by the CO2 stimulation of plant biomass. Our results highlight the interdependence of element cycles and the importance of taking a broad view of the periodic table when the effects of global environmental change on ecosystem biogeochemistry are considered.

  7. Exchange of adsorbed H2O and CO2 between the regolith and atmosphere of Mars caused by changes in surface insolation

    NASA Technical Reports Server (NTRS)

    Fanale, F. P.; Cannon, W. A.

    1974-01-01

    Estimates have been made of the capacity of the Martian regolith to exchange adsorbed H2O and CO2 with the atmosphere-plus-cap system (APCS). These estimates are based upon measured isotherms for H2O and CO2 adsorption on pulverized basalt at low temperatures and on theoretical considerations. A unit column (1 sq cm) of regolith with a deep subsurface temperature of -77 C, considered average for the disk, will contain about 0.4 g of adsorbed CO2 and about 1 g of adsorbed H2O per meter of depth. Under favorable circumstances the top 3 cm can exchange much more H2O with the lower atmosphere each day than is necessary to produce the diurnal brightening. The process appears to be seasonally reversible. The total regolith may contain, in the adsorbed phase alone, as much as 1% of the H2O and 5% of the CO2 surface inventories expected for a hypothetical Mars that has experienced degassing as intensive as that of earth.

  8. Elevated atmospheric CO2 concentration leads to increased whole-plant isoprene emission in hybrid aspen (Populus tremula × Populus tremuloides).

    PubMed

    Sun, Zhihong; Niinemets, Ülo; Hüve, Katja; Rasulov, Bahtijor; Noe, Steffen M

    2013-05-01

    Effects of elevated atmospheric [CO2] on plant isoprene emissions are controversial. Relying on leaf-scale measurements, most models simulating isoprene emissions in future higher [CO2] atmospheres suggest reduced emission fluxes. However, combined effects of elevated [CO2] on leaf area growth, net assimilation and isoprene emission rates have rarely been studied on the canopy scale, but stimulation of leaf area growth may largely compensate for possible [CO2] inhibition reported at the leaf scale. This study tests the hypothesis that stimulated leaf area growth leads to increased canopy isoprene emission rates. We studied the dynamics of canopy growth, and net assimilation and isoprene emission rates in hybrid aspen (Populus tremula × Populus tremuloides) grown under 380 and 780 μmol mol(-1) [CO2]. A theoretical framework based on the Chapman-Richards function to model canopy growth and numerically compare the growth dynamics among ambient and elevated atmospheric [CO2]-grown plants was developed. Plants grown under elevated [CO2] had higher C : N ratio, and greater total leaf area, and canopy net assimilation and isoprene emission rates. During ontogeny, these key canopy characteristics developed faster and stabilized earlier under elevated [CO2]. However, on a leaf area basis, foliage physiological traits remained in a transient state over the whole experiment. These results demonstrate that canopy-scale dynamics importantly complements the leaf-scale processes, and that isoprene emissions may actually increase under higher [CO2] as a result of enhanced leaf area production. © 2013 The Authors. New Phytologist © 2013 New Phytologist Trust.

  9. Transition metal atoms absorbed on MoS2/h-BN heterostructure: stable geometries, band structures and magnetic properties.

    PubMed

    Wu, Yanbing; Huang, Zongyu; Liu, Huating; He, Chaoyu; Xue, Lin; Qi, Xiang; Zhong, Jianxin

    2018-06-15

    We have studied the stable geometries, band structures and magnetic properties of transition-metal (V, Cr, Mn, Fe, Co and Ni) atoms absorbed on MoS2/h-BN heterostructure systems by first-principles calculations. By comparing the adsorption energies, we find that the adsorbed transition metal (TM) atoms prefer to stay on the top of Mo atoms. The results of the band structure without spin-orbit coupling (SOC) interaction indicate that the Cr-absorbed systems behave in a similar manner to metals, and the Co-absorbed system exhibits a half-metallic state. We also deduce that the V-, Mn-, Fe-absorbed systems are semiconductors with 100% spin polarization at the HOMO level. The Ni-absorbed system is a nonmagnetic semiconductor. In contrast, the Co-absorbed system exhibits metallic state, and the bandgap of V-absorbed system decreases slightly according to the SOC calculations. In addition, the magnetic moments of all the six TM atoms absorbed on the MoS2/h-BN heterostructure systems decrease when compared with those of their free-standing states.

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

    NASA Astrophysics Data System (ADS)

    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

  11. An 8-Year, High-Resolution Reanalysis of Atmospheric CO2 Mixing Ratios Based on OCO-2 and GOSAT-ACOS Retrievals

    NASA Technical Reports Server (NTRS)

    Weir, B.; Chatterjee, A.; Ott, L. E.; Pawson, S.

    2017-01-01

    The NASA GMAO (Global Modeling and Assimilation Office) reanalysis blends OCO-2 (Orbiting Carbon Observatory 2) and GOSAT-ACOS (Greenhouse Gases Observing Satellite-Atmospheric Carbon Observations from Space) retrievals (top) with GEOS (Goddard Earth Observing System) model predictions (bottom) to estimate the full 3D (three-dimensional) state of CO2 every 3 hours (middle). This poster describes monthly atmospheric growth rates derived from the reanalysis and an application to aircraft data with the potential to aid bias correction.

  12. Tree species influence soil-atmosphere fluxes of the greenhouse gases CO2, CH4 and N2O

    NASA Astrophysics Data System (ADS)

    Steffens, Christina; Vesterdal, Lars; Pfeiffer, Eva-Maria

    2016-04-01

    In the temperate zone, forests are the greatest terrestrial sink for atmospheric CO2, and tree species affect soil C stocks and soil CO2 emissions. When considering the total greenhouse gas (GHG) balance of the forest soil, the relevant GHGs CH4 and N2O should also be considered as they have a higher global warming potential than CO2. The presented data are first results from a field study in a common garden site in Denmark where tree species with ectomycorrhizal colonization (beech - Fagus sylvatica, oak - Quercus robur) and with arbuscular mycorrhizal colonization (maple - Acer pseudoplatanus, ash - Fraxinus excelsior) have been planted in monocultures in adjacent blocks of about 0.25 ha in the year 1973 on former arable land. The soil-atmosphere fluxes of all three gases were measured every second week since August 2015. The hypothesis is that the total GHG efflux from forest soil would differ between species, and that these differences could be related to the type of mycorrhizal association and leaf litter quality. Preliminary results (August to December 2015) indicate that tree species influence the fluxes (converted to CO2-eq) of the three GHGs. Total soil CO2 efflux was in the low end of the range reported for temperate broadleaved forests but similar to the measurements at the same site approximately ten years ago. It was highest under oak (9.6±2.4 g CO2 m-2 d-1) and lowest under maple (5.2±1.6 g CO2 m-2 d-1). In contrast, soil under oak was a small but significant sink for CH4(-0.005±0.003 g CO2-eq m-2 d-1), while there were almost no detectable CH4 fluxes in maple. Emissions of N2O were highest under beech (0.6±0.6 g CO2-eq m-2 d-1) and oak (0.2±0.09 g CO2-eq m-2 d-1) and lowest under ash (0.03±0.04 g CO2-eq m-2 d-1). In the total GHG balance, soil CH4 uptake was negligible (≤0.1% of total emissions). Emissions of N2O (converted to CO2-eq) contributed <1% (ash) to 8% (beech) to total GHG emissions. Summing up all GHG emissions, the tree species

  13. Carbon Disulfide (CS2) Mechanisms in Formation of Atmospheric Carbon Dioxide (CO2) Formation from Unconventional Shale Gas Extraction and Processing Operations and Global Climate Change.

    PubMed

    Rich, Alisa L; Patel, Jay T

    2015-01-01

    Carbon disulfide (CS2) has been historically associated with the production of rayon, cellophane, and carbon tetrachloride. This study identifies multiple mechanisms by which CS2 contributes to the formation of CO2 in the atmosphere. CS2 and other associated sulfide compounds were found by this study to be present in emissions from unconventional shale gas extraction and processing (E&P) operations. The breakdown products of CS2; carbonyl sulfide (COS), carbon monoxide (CO), and sulfur dioxide (SO2) are indirect greenhouse gases (GHGs) that contribute to CO2 levels in the atmosphere. The heat-trapping nature of CO2 has been found to increase the surface temperature, resulting in regional and global climate change. The purpose of this study is to identify five mechanisms by which CS2 and the breakdown products of CS2 contribute to atmospheric concentrations of CO2. The five mechanisms of CO2 formation are as follows: Chemical Interaction of CS2 and hydrogen sulfide (H2S) present in natural gas at high temperatures, resulting in CO2 formation;Combustion of CS2 in the presence of oxygen producing SO2 and CO2;Photolysis of CS2 leading to the formation of COS, CO, and SO2, which are indirect contributors to CO2 formation;One-step hydrolysis of CS2, producing reactive intermediates and ultimately forming H2S and CO2;Two-step hydrolysis of CS2 forming the reactive COS intermediate that reacts with an additional water molecule, ultimately forming H2S and CO2. CS2 and COS additionally are implicated in the formation of SO2 in the stratosphere and/or troposphere. SO2 is an indirect contributor to CO2 formation and is implicated in global climate change.

  14. Effects of salinity and short-term elevated atmospheric CO2 on the chemical equilibrium between CO2 fixation and photosynthetic electron transport of Stevia rebaudiana Bertoni.

    PubMed

    Hussin, Sayed; Geissler, Nicole; El-Far, Mervat M M; Koyro, Hans-Werner

    2017-09-01

    The effect of water salinity on plant growth and photosynthetic traits of Stevia rebaudiana was investigated to determine its level and mechanisms of salinity tolerance. It was also attempted to assess how short-term elevated CO 2 concentration would influence the boundaries and mechanisms of its photosynthetic capacity. The plants were grown in gravel/hydroponic system under controlled greenhouse conditions and irrigated with four different salinity levels (0, 25, 50 and 100 mol m -3 NaCl). Low salinity did not significantly alter the plant fresh weight, which was substantially decreased by 67% at high salinity treatment. Salinity tolerance threshold was reached at 50 mol m -3  NaCl while C50 was between 50 and 100 mol m -3  NaCl, indicating that S. rebaudiana is a moderate salt tolerant species. Salt-induced growth reduction was apparently linked to a significant decline of about 47% in the photosynthetic rates (A net ) at high salinity treatment, leading consequently to a disequilibrium between CO 2 -assimilation and electron transport rates (indicated by enhanced ETR max /A gross ratio). Elevated atmospheric CO 2 enhanced CO 2 assimilation rates by 65% and 80% for control and high-salt-stressed plants respectively, likely due to significant increases in intercellular CO 2 concentration (indicated by enhanced C i /C a ). The priority for Stevia under elevated atmospheric CO 2 was not to save water but to maximize photosynthesis so that the PWUE was progressively improved and the threat of oxidative stress was diminished (decline in ETR max /A gross ). The results imply that elevated CO 2 level could ameliorate some of the detrimental effects of salinity, conferring higher tolerance and survival of S. rebaudiana, a highlydesired feature with the forthcoming era of global changes. Copyright © 2017 Elsevier Masson SAS. All rights reserved.

  15. Graphene/Poly(aniline-co-pyrrole) Nanocomposite: Potential Candidate for Supercapacitor and Microwave Absorbing Applications.

    PubMed

    Sahoo, Sumanta; Bhattacharya, Pallab; Dhibar, Saptarshi; Hatui, Goutam; Das, Tanya; Das, Chapal Kumar

    2015-09-01

    A simple and cost-effective in-situ chemical route to prepare the nanocomposites based on graphene and Poly(aniline-co-pyrrole) [PPP] has been proposed. Introduction of graphene changes the morphology of copolymer from spherical to fiber like. Graphene/Poly(aniline-co-pyrrole) [GPPP] nanocomposite achieved highest specific capacitance of 351 F/g and energy density of 124.8 Wh/Kg at 10 mV/s scan rate. The composite also obtained moderate specific capacitance retention of 66% after 500 cycles, which establish its potentiality as supercapacitor electrode materials. The composite also exhibited high electrical conductivity and superior microwave absorbing properties (maximum reflection loss is -29.97 dB). The absorption range corresponding to ≥ 90% absorption (or -10 dB) is 2.72 GHz which is excellent for the microwave absorbing applications.

  16. [Effect of atmospheric CO2 concentration and nitrogen application level on absorption and transportation of nutrient elements in oilseed rape].

    PubMed

    Wang, Wen-ming; Zhang, Zhen-hua; Song, Hai-xing; Liu, Qiang; Rong, Xiang-min; Guan, Chun-yun; Zeng, Jing; Yuan, Dan

    2015-07-01

    Effect of elevated atmospheric-CO2 (780 µmol . mol-1) on the absorption and transportation of secondary nutrient elements (calcium, magnesium, sulphur) and micronutrient elements (iron, manganese, zinc, molybdenum and boron) in oilseed rape at the stem elongation stage were studied by greenhouse simulated method. Compared with the ambient CO2 condition, the content of Zn in stem was increased and the contents of other nutrient elements were decreased under the elevated atmospheric-CO2 with no nitrogen (N) application; the contents of Ca, S, B and Zn were increased, and the contents of Mg, Mn, Mo and Fe were decreased under the elevated atmospheric CO2 with N application (0.2 g N . kg-1 soil); except the content of Mo in leaf was increased, the contents of other nutrient elements were decreased under the elevated atmospheric-CO2 with two levels of N application. Compared with the ambient CO2 condition, the amounts of Ca and S relative to the total amount of secondary nutrient elements in stem and the amounts of B and Zn relative to the total amount of micronutrient elements in stem were increased under the elevated-CO2 treatment with both levels of N application, and the corresponding values of Mg, Fe, Mn and Mo were decreased; no-N application treatment increased the proportion of Ca distributed into the leaves, and the proportion of Mg distributed into leaves was increased by the normal-N application level; the proportions of Mn, Zn and Mo distributed into the leaves were increased at both N application levels. Without N application, the elevation of atmospheric CO2 increased the transport coefficients of SFe, Mo and SS,B, but decreased the transport coefficients of SMg,Fe, SMg, Mn and SS,Fe, indicating the proportions of Mo, S transported into the upper part of plant tissues was higher than that of Fe, and the corresponding value of B was higher than that observed for S, the corresponding value of Mg was higher than that of Fe and Mn. Under normal-N application

  17. Microbial Reverse-Electrodialysis Electrolysis and Chemical-Production Cell for H2 Production and CO2 Sequestration.

    PubMed

    Zhu, Xiuping; Hatzell, Marta C; Logan, Bruce E

    2014-04-08

    Natural mineral carbonation can be accelerated using acid and alkali solutions to enhance atmospheric CO 2 sequestration, but the production of these solutions needs to be carbon-neutral. A microbial reverse-electrodialysis electrolysis and chemical-production cell (MRECC) was developed to produce these solutions and H 2 gas using only renewable energy sources (organic matter and salinity gradient). Using acetate (0.82 g/L) as a fuel for microorganisms to generate electricity in the anode chamber (liquid volume of 28 mL), 0.45 mmol of acid and 1.09 mmol of alkali were produced at production efficiencies of 35% and 86%, respectively, along with 10 mL of H 2 gas. Serpentine dissolution was enhanced 17-87-fold using the acid solution, with approximately 9 mL of CO 2 absorbed and 4 mg of CO 2 fixed as magnesium or calcium carbonates. The operational costs, based on mineral digging and grinding, and water pumping, were estimated to be only $25/metric ton of CO 2 fixed as insoluble carbonates. Considering the additional economic benefits of H 2 generation and possible wastewater treatment, this method may be a cost-effective and environmentally friendly method for CO 2 sequestration.

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

    NASA Astrophysics Data System (ADS)

    Lac, C.; Donnelly, R. P.; Masson, V.; Pal, S.; Donier, S.; Queguiner, S.; Tanguy, G.; Ammoura, L.; Xueref-Remy, I.

    2012-10-01

    Accurate simulation of the spatial and temporal variability of tracer mixing ratios over urban areas is challenging, but essential in order to utilize CO2 measurements in an atmospheric inverse framework 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 between the surface and the atmosphere. Statistical scores show a good representation of the Urban Heat Island (UHI) and urban-rural contrasts. Boundary layer heights (BLH) at urban, sub-urban and rural sites are well captured, especially the onset time of the BLH increase and its growth rate in the morning, that are essential for tall tower CO2 observatories. Only nocturnal BLH at sub-urban sites are slightly underestimated a few nights, with a bias less than 50 m. At 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. The timing of the CO2 cycle is well captured by the model, with only small biases on CO2 concentrations, mainly linked to the misrepresentation of anthropogenic emissions, as the Eiffel site is at the heart of trafic emission sources. At sub-urban ground stations, CO2 measurements exhibit maxima at the beginning and at the end of each night, when the ABL is fully contracted, with a very strong spatio-temporal variability. The CO2 cycle at these sites is generally well reproduced by the model, even if some biases on the nocturnal maxima appear in the Paris plume parly due to small errors on the vertical transport, or in

  19. Seasonal change in CO2 and H2O exchange between grassland and atmosphere

    NASA Astrophysics Data System (ADS)

    Saigusa, N.; Liu, S.; Oikawa, T.; Watanabe, T.

    1996-03-01

    The seasonal change in CO2 flux over an artificial grassland was analyzed from the ecological and meteorological point of view. This grassland contains C3 and C4 plants; the three dominant species belonging to the Gramineae; Festuca elatior (C3) dominated in early spring, and Imperata cylindrica (C4) and Andropogon virginicus (C4) grew during early summer and became dominant in mid-summer. CO2 flux was measured by the gradient method, and the routinely observed data for the surface-heat budget were used to analyze the CO2 and H2O exchange between the grassland and atmosphere. From August to October in 1993, CO2 flux was reduced to around half under the same solar-radiation conditions, while H2O flux decreased 20% during the same period. The monthly values of water use efficiency, i.e., ratio of CO2 flux to H2O flux decreased from 5.8 to 3.3 mg CO2/g H2O from August to October, the Bowen ratio increased from 0.20 to 0.30, and the ratio of the bulk latent heat transfer coefficient CE to the sensible heat transfer coefficient CH was maintained around 0.40-0.50. The increase in the Bowen ratio was explained by the decrease in air temperature from 22.3 °C in August to 16.6 °C in October without considering biological effects such as stomatal closure on the individual leaves. The nearly constant CE/CH ratios suggested that the contribution ratio of canopy resistance to aerodynamic resistance did not change markedly, although the meteorological conditions changed seasonally. The decrease in the water use efficiency, however, suggested that the photosynthetic rate decreased for individual leaves from August to October under the same radiation conditions. Diurnal variations of CO2 exchange were simulated by the multi-layer canopy model taking into account the differences in the stomatal conductance and photosynthetic pathway between C3 and C4 plants. The results suggested that C4 plants played a major role in the CO2 exchange in August, the contribution of C4 plants

  20. The role of carbon dust emission as a global source of atmospheric CO2

    USDA-ARS?s Scientific Manuscript database

    Soil erosion redistributes soil organic carbon (SOC) within terrestrial ecosystems, to the atmosphere and oceans. Dust export is an essential component of the carbon (C) and carbon dioxide (CO2) budget, because wind erosion contributes to the C cycle by selectively removing4 SOC from vast areas and ...