Regional Ecosystem-Atmosphere CO2 Exchange Via Atmospheric Budgets

Energy Technology Data Exchange (ETDEWEB)

Davis, K J; Richardson, S J; Miles, N L

2007-03-07

Inversions of atmospheric CO2 mixing ratio measurements to determine CO2 sources and sinks are typically limited to coarse spatial and temporal resolution. This limits our ability to evaluate efforts to upscale chamber- and stand-level CO2 flux measurements to regional scales, where coherent climate and ecosystem mechanisms govern the carbon cycle. As a step towards the goal of implementing atmospheric budget or inversion methodology on a regional scale, a network of five relatively inexpensive CO2 mixing ratio measurement systems was deployed on towers in northern Wisconsin. Four systems were distributed on a circle of roughly 150-km radius, surrounding one centrally located system at the WLEF tower near Park Falls, WI. All measurements were taken at a height of 76 m AGL. The systems used single-cell infrared CO2 analyzers (Licor, model LI-820) rather than the siginificantly more costly two-cell models, and were calibrated every two hours using four samples known to within ± 0.2 ppm CO2. Tests prior to deployment in which the systems sampled the same air indicate the precision of the systems to be better than ± 0.3 ppm and the accuracy, based on the difference between the daily mean of one system and a co-located NOAA-ESRL system, is consistently better than ± 0.3 ppm. We demonstrate the utility of the network in two ways. We interpret regional CO2 differences using a Lagrangian parcel approach. The difference in the CO2 mixing ratios across the network is at least 2-3 ppm, which is large compared to the accuracy and precision of the systems. Fluxes estimated assuming Lagrangian parcel transport are of the same sign and magnitude as eddy-covariance flux measurements at the centrally-located WLEF tower. These results indicate that the network will be useful in a full inversion model. Second, we present a case study involving a frontal passage through the region. The progression of a front across the network is evident; changes as large as four ppm in one minute

ISLSCP II Globalview: Atmospheric CO2 Concentrations

Data.gov (United States)

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

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

Science.gov (United States)

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

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

International Nuclear Information System (INIS)

Nagai, Haruyasu

2004-11-01

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

Role of Atmospheric CO2 in the Ice Ages (Invited)

Science.gov (United States)

Toggweiler, J. R.

2010-12-01

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

Atmospheric verification of anthropogenic CO2 emission trends

Science.gov (United States)

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

2013-05-01

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

Positive feedback between increasing atmospheric CO2 and ecosystem productivity

Science.gov (United States)

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

2009-12-01

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

CO2 emission calculations and trends

International Nuclear Information System (INIS)

Boden, T.A.; Marland, G.; Andres, R.J.

1995-01-01

Evidence that the atmospheric CO 2 concentration has risen during the past several decades is irrefutable. Most of the observed increase in atmospheric CO 2 is believed to result from CO 2 releases from fossil-fuel burning. The United Nations (UN) Framework Convention on Climate Change (FCCC), signed in Rio de Janeiro in June 1992, reflects global concern over the increasing CO 2 concentration and its potential impact on climate. One of the convention's stated objectives was the ''stabilization of greenhouse gas concentrations in the atmosphere at a level that would prevent dangerous anthropogenic interference with the climate system. '' Specifically, the FCCC asked all 154 signing countries to conduct an inventory of their current greenhouse gas emissions, and it set nonbinding targets for some countries to control emissions by stabilizing them at 1990 levels by the year 2000. Given the importance of CO 2 as a greenhouse gas, the relationship between CO 2 emissions and increases in atmospheric CO 2 levels, and the potential impacts of a greenhouse gas-induced climate change; it is important that comprehensive CO 2 emissions records be compiled, maintained, updated, and documented

Spectroscopic technique for measuring atmospheric CO2

International Nuclear Information System (INIS)

Stokes, G.M.; Stokes, R.A.

1979-01-01

As part of a continuing effort to identify areas in which astronomical techniques and data may be profitably applied to atmospheric problems, both new and archival solar spectra have been collected to prepare for an analysis of their use for studying the changes of the atmospheric CO 2 burden. This analysis has resulted in the initiation of an observing program using the Fourier Transform Spectrometer (FTS) of the McMath Solar Telescope at Kitt Peak National Observatory (KPNO). This program is generating spectra, the quality of which should not only aid the archival CO 2 study but also lead to analyses of other trace gases

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

Directory of Open Access Journals (Sweden)

H. A. J. Meijer

2009-09-01

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

CO{sub 2} emission calculations and trends

Energy Technology Data Exchange (ETDEWEB)

Boden, T.A.; Marland, G. [Oak Ridge National Lab., TN (United States); Andres, R.J. [Alaska Univ., Fairbanks, AK (United States). Inst. of Northern Engineering

1995-12-31

Evidence that the atmospheric CO{sub 2} concentration has risen during the past several decades is irrefutable. Most of the observed increase in atmospheric CO{sub 2} is believed to result from CO{sub 2} releases from fossil-fuel burning. The United Nations (UN) Framework Convention on Climate Change (FCCC), signed in Rio de Janeiro in June 1992, reflects global concern over the increasing CO{sub 2} concentration and its potential impact on climate. One of the convention`s stated objectives was the ``stabilization of greenhouse gas concentrations in the atmosphere at a level that would prevent dangerous anthropogenic interference with the climate system. `` Specifically, the FCCC asked all 154 signing countries to conduct an inventory of their current greenhouse gas emissions, and it set nonbinding targets for some countries to control emissions by stabilizing them at 1990 levels by the year 2000. Given the importance of CO{sub 2} as a greenhouse gas, the relationship between CO{sub 2} emissions and increases in atmospheric CO{sub 2} levels, and the potential impacts of a greenhouse gas-induced climate change; it is important that comprehensive CO{sub 2} emissions records be compiled, maintained, updated, and documented.

CO{sub 2} Emission Calculations and Trends

Science.gov (United States)

Boden, T. A.; Marland, G.; Andres, R. J.

1995-06-01

Evidence that the atmospheric CO{sub 2}concentration has risen during the past several decades is irrefutable. Most of the observed increase in atmospheric CO{sub 2} is believed to result from CO{sub 2} releases from fossil-fuel burning. The United Nations (UN) Framework Convention on Climate Change (FCCC), signed in Rio de Janeiro in June 1992, reflects global concern over the increasing CO{sub 2} concentration and its potential impact on climate. One of the convention`s stated objectives was the stabilization of greenhouse gas concentrations in the atmosphere at a level that would prevent dangerous anthropogenic interference with the climate system. Specifically, the FCCC asked all 154 signing countries to conduct an inventory of their current greenhouse gas emissions, and it set nonbinding targets for some countries to control emissions by stabilizing them at 1990 levels by the year 2000. Given the importance of CO{sub 2} as a greenhouse gas, the relationship between CO{sub 2} emissions and increases in atmospheric CO{sub 2} levels, and the potential impacts of a greenhouse gas-induced climate change; it is important that comprehensive CO{sub 2} emissions records be compiled, maintained, updated, and documented.

Fossil fuel CO2 estimation by atmospheric 14C measurement and CO2 mixing ratios in the city of Debrecen, Hungary

International Nuclear Information System (INIS)

Molnar, M.; Svingor, E.; Haszpra, L.; Ivo Svetlik; Veres, M.

2010-01-01

A field unit was installed in the city of Debrecen (East Hungary) during the summer of 2008 to monitor urban atmospheric fossil fuel CO 2 . To establish a reference level simultaneous CO 2 sampling has been carried out at a rural site (Hegyhatsal) in Western Hungary. Using the Hungarian background 14 CO 2 observations from the rural site atmospheric fossil fuel CO 2 component for the city of Debrecen was reported in a regional 'Hungarian' scale. A well visible fossil fuel CO 2 peak (10-15 ppm) with a maximum in the middle of winter 2008 (January) was observed in Debrecen air. Significant local maximum (∼20 ppm) in fossil fuel CO 2 during Octobers of 2008 and 2009 was also detected. Stable isotope results are in agreement with the 14 C based fossil fuel CO 2 observations as the winter of 2008 and 2009 was different in atmospheric δ 13 C variations too. The more negative δ 13 C of atmospheric CO 2 in the winter of 2008 means more fossil carbon in the atmosphere than during the winter of 2009. (author)

Net uptake of atmospheric CO2 by coastal submerged aquatic vegetation

Science.gov (United States)

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

2014-01-01

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

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

Science.gov (United States)

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

2017-03-01

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

The millennial atmospheric lifetime of anthropogenic CO2

International Nuclear Information System (INIS)

Archer, D.

2008-01-01

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

Atmospheric CO2 and abrupt climate change on submillennial timescales

Science.gov (United States)

Ahn, Jinho; Brook, Edward

2010-05-01

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

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

Science.gov (United States)

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

Water loss from terrestrial planets with CO2-rich atmospheres

International Nuclear Information System (INIS)

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

2013-01-01

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

Simulated effect of calcification feedback on atmospheric CO2 and ocean acidification

Science.gov (United States)

Zhang, Han; Cao, Long

2016-01-01

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

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

Energy Technology Data Exchange (ETDEWEB)

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

1992-09-01

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

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

International Nuclear Information System (INIS)

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

2014-01-01

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

Stable isotope measurements of atmospheric CO2

International Nuclear Information System (INIS)

White, J.W.C.; Ferretti, D.F.; Vaughn, B.H.; Francey, R.J.; Allison, C.E.

2002-01-01

The measurement of stable carbon isotope ratios of atmospheric carbon dioxide, δ 13 CO 2 are useful for partitioning surface-atmospheric fluxes into terrestrial and oceanic components. δC 18 OO also has potential for segregating photosynthetic and respiratory fluxes in terrestrial ecosystems. Here we describe in detail the techniques for making these measurements. The primary challenge for all of the techniques used to measure isotopes of atmospheric CO 2 is to achieve acceptable accuracy and precision and to maintain them over the decades needed to observe carbon cycle variability. The keys to success such an approach are diligent intercalibrations of laboratories from around the world, as well as the use of multiple techniques such as dual inlet and GC-IRMS and the intercomparison of such measurements. We focus here on two laboratories, the Stable Isotope Lab at the Institute for Arctic and Alpine Research (INSTAAR) at the University of Colorado is described and the Commonwealth Scientific and Industrial Research Organisation - Atmospheric Research (CSIRO). Different approaches exist at other laboratories (e.g. programs operated by Scripps Institution of Oceanography (SIO) and The Center for Atmospheric and Oceanic Studies, Toboku University (TU)) however these are not discussed here. Finally, we also discuss the recently developed Gas Chromatography - Isotope Ratio Mass Spectrometry (GC-IRMS) technique which holds significant promise for measuring ultra-small samples of gas with good precision. (author)

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

Science.gov (United States)

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

2016-10-01

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

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

Science.gov (United States)

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

1979-01-01

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

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

OpenAIRE

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

2012-01-01

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

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

Science.gov (United States)

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

2000-09-21

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

Modeling the transformation of atmospheric CO2 into microalgal biomass.

Science.gov (United States)

Hasan, Mohammed Fahad; Vogt, Frank

2017-10-23

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

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

DEFF Research Database (Denmark)

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

2017-01-01

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

Detection of CO2 leaks from carbon capture and storage sites with combined atmospheric CO2 and O-2 measurements

NARCIS (Netherlands)

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

2015-01-01

This paper presents a transportable instrument that simultaneously measures the CO2 and (relative) O-2 concentration of the atmosphere with the purpose to aid in the detection of CO2 leaks from CCS sites. CO2 and O-2 are coupled in most processes on earth (e.g., photosynthesis, respiration and

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

Science.gov (United States)

Fleischer, Siegfried

2003-02-01

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

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

Energy Technology Data Exchange (ETDEWEB)

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

2013-12-01

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

State of the Carbon Cycle - Consequences of Rising Atmospheric CO2

Science.gov (United States)

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

2016-12-01

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

State of the Carbon Cycle - Consequences of Rising Atmospheric CO2

Science.gov (United States)

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

CO2 cycle

Science.gov (United States)

Titus, Timothy N.; Byrne, Shane; Colaprete, Anthony; Forget, Francois; Michaels, Timothy I.; Prettyman, Thomas H.

2017-01-01

This chapter discusses the use of models, observations, and laboratory experiments to understand the cycling of CO2 between the atmosphere and seasonal Martian polar caps. This cycle is primarily controlled by the polar heat budget, and thus the emphasis here is on its components, including solar and infrared radiation, the effect of clouds (water- and CO2-ice), atmospheric transport, and subsurface heat conduction. There is a discussion about cap properties including growth and regression rates, albedos and emissivities, grain sizes and dust and/or water-ice contamination, and curious features like cold gas jets and araneiform (spider-shaped) terrain. The nature of the residual south polar cap is discussed as well as its long-term stability and ability to buffer atmospheric pressures. There is also a discussion of the consequences of the CO2 cycle as revealed by the non-condensable gas enrichment observed by Odyssey and modeled by various groups.

The equilibrium response to doubling atmospheric CO2

International Nuclear Information System (INIS)

Mitchell, J.F.B.

1990-01-01

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

The millennial atmospheric lifetime of anthropogenic CO{sub 2}

Energy Technology Data Exchange (ETDEWEB)

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

2008-10-15

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

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

Science.gov (United States)

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

2016-05-01

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

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

International Nuclear Information System (INIS)

Zhang, Wendong; Dong, Fan; Zhang, Wei

2015-01-01

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

Thermodynamic stability and guest distribution of CH4/N2/CO2 mixed hydrates for methane hydrate production using N2/CO2 injection

International Nuclear Information System (INIS)

Lim, Dongwook; Ro, Hyeyoon; Seo, Yongwon; Seo, Young-ju; Lee, Joo Yong; Kim, Se-Joon; Lee, Jaehyoung; Lee, Huen

2017-01-01

Highlights: • We examine the thermodynamic stability and guest distribution of CH 4 /N 2 /CO 2 mixed hydrates. • Phase equilibria of the CH 4 /N 2 /CO 2 mixed hydrates were measured to determine the thermodynamic stability. • The N 2 /CO 2 ratio of the hydrate phase is almost constant despite the enrichment of CO 2 in the hydrate phase. • 13 C NMR results indicate the preferential occupation of N 2 and CO 2 in the small and large cages of sI hydrates, respectively. - Abstract: In this study, thermodynamic stability and cage occupation behavior in the CH 4 – CO 2 replacement, which occurs in natural gas hydrate reservoirs by injecting flue gas, were investigated with a primary focus on phase equilibria and composition analysis. The phase equilibria of CH 4 /N 2 /CO 2 mixed hydrates with various compositions were measured to determine the thermodynamic stability of gas hydrate deposits replaced by N 2 /CO 2 gas mixtures. The fractional experimental pressure differences (Δp/p) with respect to the CSMGem predictions were found to range from −0.11 to −0.02. The composition analysis for various feed gas mixtures with a fixed N 2 /CO 2 ratio (4.0) shows that CO 2 is enriched in the hydrate phase, and the N 2 /CO 2 ratio in the hydrate phase is independent of the feed CH 4 fractions. Moreover, 13 C NMR measurements indicate that N 2 molecules preferentially occupy the small 5 12 cages of sI hydrates while the CO 2 molecules preferentially occupy the large 5 12 6 2 cages, resulting in an almost constant area ratio of CH 4 molecules in the large to small cages of the CH 4 /N 2 /CO 2 mixed hydrates. The overall experimental results provide a better understanding of stability conditions and guest distributions in natural gas hydrate deposits during CH 4 – flue gas replacement.

Do Continental Shelves Act as an Atmospheric CO2 Sink?

Science.gov (United States)

Cai, W.

2003-12-01

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

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

Directory of Open Access Journals (Sweden)

N. Chandra

2016-05-01

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

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

International Nuclear Information System (INIS)

Karnosky, D.F.

2003-06-01

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

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

Science.gov (United States)

Oschlies, A.

2009-08-01

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

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

Science.gov (United States)

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

2016-12-01

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

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

Science.gov (United States)

Shaw, G. H.

2009-12-01

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

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

Science.gov (United States)

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

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

Energy Technology Data Exchange (ETDEWEB)

Oechel, Walter C.

1990-09-05

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

The photochemical stability of the Venus atmosphere against UV radiation

International Nuclear Information System (INIS)

Mills, F.P.; Slanger, T.G.; Allen, M.

2004-01-01

Full text: One unresolved question regarding the Venus atmosphere is what chemical mechanism(s) stabilize its primary constituent (CO 2 ) against UV radiation. CO 2 photolyzes on the day side into CO and O after absorbing photons at 2 rather than recombining with CO to form CO 2 , and the intense night side O 2 airglow observed quantitatively supports this. CO and O 2 are photochemically stable in an otherwise pure CO 2 atmosphere so significant abundances of CO and O 2 could accumulate on Venus if no catalytic mechanism existed to speed the reformation of CO 2 . However, the observational upper limit on ground state O 2 is equivalent to 2 from CO and O 2 . Recent laboratory work verified the existence of the ClC(O)OO catalytic mechanism that has been used in photochemical models since the early 1980s. However, there are significant uncertainties in the rates for the component steps of this catalytic mechanism. An alternative mechanism for production of CO 2 that has not previously been modeled but which could be competitive with the ClCO(O)O mechanism is the reaction CO + O 2 (c 1 Σ - u ) → CO 2 + O( 1 D) or O( 1 S), Reaction (1). A range of values for Reaction (1) will be examined in model calculations to compare with observational (UV to IR) constraints and to assess under what conditions this mechanism is competitive with the ClC(O)OO catalytic mechanism. The sensitivity of the results to uncertainties in the CO 2 UV absorption cross section also will be examined

A role for atmospheric CO2 in preindustrial climate forcing

NARCIS (Netherlands)

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

2008-01-01

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

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

International Nuclear Information System (INIS)

Olsen, Are; Anderson, Leif G.

2002-01-01

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

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

International Nuclear Information System (INIS)

Yamada, Yoshimune; Yasuike, Kaeko; Komura, Kazuhisa

2008-01-01

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

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

Science.gov (United States)

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

2016-11-01

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

Sensitivity Analysis for Atmospheric Infrared Sounder (AIRS) CO2 Retrieval

Science.gov (United States)

Gat, Ilana

2012-01-01

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

The extraction of CO2 from the atmosphere

International Nuclear Information System (INIS)

Hauet, Jean-Pierre

2014-01-01

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

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

Science.gov (United States)

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

2015-01-01

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

Biomass burial and storage to reduce atmospheric CO2

Science.gov (United States)

Zeng, N.

2012-04-01

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

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

International Nuclear Information System (INIS)

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

2002-01-01

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

Deep Sea Memory of High Atmospheric CO2 Concentration

Science.gov (United States)

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

2015-04-01

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

Elevated atmospheric CO2 concentration leads to increased whole-plant isoprene emission in hybrid aspen (Populus tremula × Populus tremuloides).

Science.gov (United States)

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.

Frequency stabilization of a 2.05 μm laser using hollow-core fiber CO2 frequency reference cell

Science.gov (United States)

Meras, Patrick; Poberezhskiy, Ilya Y.; Chang, Daniel H.; Spiers, Gary D.

2010-04-01

We have designed and built a hollow-core fiber frequency reference cell, filled it with CO2, and used it to demonstrate frequency stabilization of a 2.05 μm Tm:Ho:YLF laser using frequency modulation (FM) spectroscopy technique. The frequency reference cell is housed in a compact and robust hermetic package that contains a several meter long hollow-core photonic crystal fiber optically coupled to index-guiding fibers with a fusion splice on one end and a mechanical splice on the other end. The package has connectorized fiber pigtails and a valve used to evacuate, refill it, or adjust the gas pressure. We have demonstrated laser frequency standard deviation decreasing from >450MHz (free-running) to laser wavelength is of particular interest for spectroscopic instruments due to the presence of many CO2 and H20 absorption lines in its vicinity. To our knowledge, this is the first reported demonstration of laser frequency stabilization at this wavelength using a hollow-core fiber reference cell. This approach enables all-fiber implementation of the optical portion of laser frequency stabilization system, thus making it dramatically more lightweight, compact, and robust than the traditional free-space version that utilizes glass or metal gas cells. It can also provide much longer interaction length of light with gas and does not require any alignment. The demonstrated frequency reference cell is particularly attractive for use in aircraft and space coherent lidar instruments for measuring atmospheric CO2 profile.

Process-based modeling of silicate mineral weathering responses to increasing atmospheric CO2 and climate change

Science.gov (United States)

Banwart, Steven A.; Berg, Astrid; Beerling, David J.

2009-12-01

A mathematical model describes silicate mineral weathering processes in modern soils located in the boreal coniferous region of northern Europe. The process model results demonstrate a stabilizing biological feedback mechanism between atmospheric CO2 levels and silicate weathering rates as is generally postulated for atmospheric evolution. The process model feedback response agrees within a factor of 2 of that calculated by a weathering feedback function of the type generally employed in global geochemical carbon cycle models of the Earth's Phanerozoic CO2 history. Sensitivity analysis of parameter values in the process model provides insight into the key mechanisms that influence the strength of the biological feedback to weathering. First, the process model accounts for the alkalinity released by weathering, whereby its acceleration stabilizes pH at values that are higher than expected. Although the process model yields faster weathering with increasing temperature, because of activation energy effects on mineral dissolution kinetics at warmer temperature, the mineral dissolution rate laws utilized in the process model also result in lower dissolution rates at higher pH values. Hence, as dissolution rates increase under warmer conditions, more alkalinity is released by the weathering reaction, helping maintain higher pH values thus stabilizing the weathering rate. Second, the process model yields a relatively low sensitivity of soil pH to increasing plant productivity. This is due to more rapid decomposition of dissolved organic carbon (DOC) under warmer conditions. Because DOC fluxes strongly influence the soil water proton balance and pH, this increased decomposition rate dampens the feedback between productivity and weathering. The process model is most sensitive to parameters reflecting soil structure; depth, porosity, and water content. This suggests that the role of biota to influence these characteristics of the weathering profile is as important, if not

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

Science.gov (United States)

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

2017-04-01

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

Atmospheric CO2 Concentration Measurements with Clouds from an Airborne Lidar

Science.gov (United States)

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.

Inter annual variability of the global carbon cycle (1992-2005) inferred by inversion of atmospheric CO2 and δ13CO2 measurements

International Nuclear Information System (INIS)

Rayner, P.J.; Pickett-Heaps, C.; Law, R.M.; Allison, C.E.; Francey, R.J.; Trudinger, C.M.

2008-01-01

We present estimates of the surface sources and sinks of CO 2 for 1992 - 2005 deduced from atmospheric inversions. We use atmospheric CO 2 records from 67 sites and 10 δ 13 CO 2 records. We use two atmospheric models to increase the robustness of the results. The results suggest that inter annual variability is dominated by the tropical land. Statistically significant variability in the tropical Pacific supports recent ocean modeling studies in that region. The northern land also shows significant variability. In particular, there is a large positive anomaly in 2003 in north Asia, which we associate with anomalous biomass burning. Results using δ 13 CO 2 and CO 2 are statistically consistent with those using only CO 2 , suggesting that it is valid to use both types of data together. An objective analysis of residuals suggests that our treatment of uncertainties in CO 2 is conservative, while those for δ 13 CO 2 are optimistic, highlighting problems in our simple isotope model. Finally, δ 13 CO 2 measurements offer a good constraint to nearby land regions, suggesting an ongoing value in these measurements for studies of inter annual variability. (authors)

Pleistocene atmospheric CO2 change linked to Southern Ocean nutrient utilization

Science.gov (United States)

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

2011-12-01

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

Sintering of dioxide pellets in an oxidizing atmosphere (CO2)

International Nuclear Information System (INIS)

Santos, G.R.T.

1992-01-01

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

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

Science.gov (United States)

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

2017-12-01

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

Regulation of senescence under elevated atmospheric CO2 via ubiquitin modification

OpenAIRE

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

2014-01-01

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

Southern hemisphere ocean CO2 uptake: reconciling atmospheric and oceanic estimates

International Nuclear Information System (INIS)

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

2003-01-01

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

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

Science.gov (United States)

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

2018-02-01

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

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

Science.gov (United States)

Xu, Ming

2015-07-20

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

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

International Nuclear Information System (INIS)

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

2014-01-01

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

Stabilization of emission of CO2: A computable general equilibrium assessment

International Nuclear Information System (INIS)

Glomsroed, S.; Vennemo, H.; Johnsen, T.

1992-01-01

A multisector computable general equilibrium model is used to study economic development perspectives in Norway if CO 2 emissions were stabilized. The effects discussed include impacts on main macroeconomic indicators and economic growth, sectoral allocation of production, and effects on the market for energy. The impact of other pollutants than CO 2 on emissions is assessed along with the related impact on noneconomic welfare. The results indicate that CO 2 emissions might be stabilized in Norway without dramatically reducing economic growth. Sectoral allocation effects are much larger. A substantial reduction in emissions to air other than CO 2 is found, yielding considerable gains in noneconomic welfare. 25 refs., 6 tabs., 2 figs

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

Science.gov (United States)

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

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

Science.gov (United States)

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

2017-12-01

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

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

Science.gov (United States)

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

2010-01-01

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

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

International Nuclear Information System (INIS)

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

2006-01-01

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

Increase of atmospheric CO2 promotes phytoplankton productivity

NARCIS (Netherlands)

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

2004-01-01

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

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

International Nuclear Information System (INIS)

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

2014-01-01

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

How Burying Biomass Can Contribute to CO2 Stabilization

Science.gov (United States)

Cook, B.; Zeng, N.; Zaitchik, B.; Gregg, J.

2008-12-01

To mitigate global climate change, a portfolio of strategies will be needed to keep the atmospheric CO2 concentration below a dangerous level. Here a carbon sequestration strategy is proposed in which certain dead or live trees are harvested via collection or selective cutting, then buried in trenches or stowed away in above-ground shelters. The largely anaerobic condition under a sufficiently thick layer of soil will prevent the decomposition of the buried wood. Because a large flux of CO2 is constantly being assimilated into the world's forests via photosynthesis, cutting off its return pathway to the atmosphere forms an effective carbon sink. It is estimated that a sustainable long-term carbon sequestration potential for wood burial is 10 ± 5 GtC y-1, and currently about 65 GtC is on the world's forest floors in the form of coarse woody debris suitable for burial. The potential is largest in tropical forests (4.2 GtC y-1), followed by temperate (3.7 GtC y-1) and boreal forests (2.1 GtC y-1). Burying wood has other benefits including minimizing CO2 source from deforestation, extending the lifetime of reforestation carbon sink, and reducing fire danger. There are possible environmental impacts such as nutrient lock-up which nevertheless appears manageable, but other environmental concerns and factors will likely set a limit so that only part of the full potential can be realized. Based on data from North American logging industry, the cost for wood burial is estimated to be 14/tCO2 (50/tC), lower than the typical cost for power plant CO2 capture with geological storage. The low cost for carbon sequestration with wood burial is possible because the technique uses the natural process of photosynthesis to remove carbon from the atmosphere. The technique is low tech, distributed, safe, and can be stopped at any time, thus an attractive option for large-scale implementation in a world-wide carbon market.

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

Science.gov (United States)

Samuels, Shanelle; Gordon, Iouli; Tan, Yan

2018-01-01

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

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

Energy Technology Data Exchange (ETDEWEB)

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

2015-12-15

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

The future role of reforestation in reducing buildup of atmospheric CO2

International Nuclear Information System (INIS)

Marland, G.

1993-01-01

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

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

Directory of Open Access Journals (Sweden)

S. Feng

2016-07-01

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

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

OpenAIRE

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

2015-01-01

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

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

Directory of Open Access Journals (Sweden)

T. J. Lueker

2004-01-01

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

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

Science.gov (United States)

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

2010-05-01

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

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

International Nuclear Information System (INIS)

Wang Xiaolin; Fu Yibei; Xie Renshou

1996-04-01

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

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

Energy Technology Data Exchange (ETDEWEB)

Ahluwalia, A.

1996-08-01

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

Atmospheric stability and atmospheric circulation in Athens, Greece

International Nuclear Information System (INIS)

Synodinou, B.M.; Petrakis, M.; Kassomenos, P.; Lykoudis, S.

1996-01-01

In the evaluation and study of atmospheric pollution reference is always made to the stability criteria. These criteria, usually represented as functions of different meteorological data such as wind speed and direction, temperature, solar radiation, etc., play a very important role in the investigation of different parameters that affect the build up of pollution episodes mainly in urban areas. In this paper an attempt is made to evaluate the atmospheric stability criteria based on measurements obtained from two locations in and nearby Athens. The atmospheric stability is then examined along with the other meteorological parameters

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

Science.gov (United States)

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

RISING ATMOSPHERIC CO2 AND CARBON SEQUESTRATION IN FORESTS

Science.gov (United States)

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

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

Science.gov (United States)

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

2015-01-01

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

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

International Nuclear Information System (INIS)

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

2014-01-01

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

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

Directory of Open Access Journals (Sweden)

J. M. Chen

2011-11-01

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

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

Energy Technology Data Exchange (ETDEWEB)

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

1993-12-31

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

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

Science.gov (United States)

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

2015-12-01

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

Investigation of the influence of atmospheric stability and turbulence on land-atmosphere exchange

Science.gov (United States)

Osibanjo, O.; Holmes, H.

2015-12-01

Surface energy fluxes are exchanged between the surface of the earth and the atmosphere and impact weather, climate, and air quality. The radiation from the sun triggers the surface-atmosphere interaction during the day as heat is transmitted to the surface and the surface heats the air directly above generating wind (i.e., thermal turbulence) that transports heat, moisture, and momentum in the atmospheric boundary layer (ABL). This process is impacted by greenhouse gasses (i.e., water vapor, carbon dioxide and other trace gases) that absorb heat emitted by the earth's surface. The concentrations of atmospheric greenhouse gasses are increasing leading to changes in ABL dynamics as a result of the changing surface energy balance. The ABL processes are important to characterize because they are difficult to parameterize in global and regional scale atmospheric models. Empirical data can be collected using eddy covariance micrometeorological methods to measure turbulent fluxes (e.g., sensible heat, moisture, and CO2) and quantify the exchange between the surface and the atmosphere. The objective of this work is to calculate surface fluxes using observational data collected during one week in September 2014 from a monitoring site in Echo, Oregon. The site is located in the Columbia Basin with rolling terrain, irrigated farmland, and over 100 wind turbines. The 10m tower was placed in a small valley depression to isolate nighttime cold air pools. This work will present observations of momentum, sensible heat, moisture, and carbon dioxide fluxes from data collected at a sampling frequency of 10Hz at four heights. Atmospheric stability is determined using Monin-Obukov length and flux Richardson number, and the impact of stability on surface-atmosphere exchange is investigated. This work will provide a better understanding of surface fluxes and mixing, particularly during stable ABL periods, and the results can be used to compare with numerical models.

ROOT-GROWTH AND FUNCTIONING UNDER ATMOSPHERIC CO2 ENRICHMENT

NARCIS (Netherlands)

STULEN, [No Value; DENHERTOG, J

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

Mars atmosphere studies with the OMEGA/Mars Express experiment: I. Overview and detection of lfuorescent emission by CO2

Science.gov (United States)

Drossart, P.; Combes, M.; Encrenaz, T.; Melchiorri, R.; Fouchet, T.; Forget, F.; Moroz, V.; Ignatiev, N.; Bibring, J.-P.; Langevin, Y.; OMEGA Team

Observations of Mars by the OMEGA/Mars Express experiment provide extended maps of the martian disk at all latitudes, and with various conditions of illumination, between 0.4 to 5 micron. The atmospheric investigations so far conducted by our team are focussed on the infrared part of the spectrum (1-5 micron), and include: the development of a correction algorithm for atmospheric gaseous absorption, to give access to fine mineralogic studies, largely decorrelated from atmospheric effects the study of dust opacity effects in the near infrared, with the aim to correct also the rough spectra from dust opacity perturbation the study of minor constituents like CO, to search for regional or global variations the study of CO2 emission at 4.3 micron related to fluorescent emission This last effect is prominently detected in limb observations obtained in 3-axis stabilized mode of Mars Express, with high altitude emission in the CO2 fundamental at 4.3 micron, usually seen in absorption in nadir observations. These emissions are related to non-LTE atmospheric layers, well above the solid surface in the mesosphere. Such emissions are also present in Earth and Venus limb observations. They are present also in nadir observations, but are reinforced in limb viewing geometry due to the tangential view. A numerical model of these emission will be presented.

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

CSIR Research Space (South Africa)

Feig, Gregor T

2016-10-01

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

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

International Nuclear Information System (INIS)

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

2002-01-01

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

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

Energy Technology Data Exchange (ETDEWEB)

Sitch, Stephen

2000-04-01

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

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

International Nuclear Information System (INIS)

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

1990-01-01

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

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

International Nuclear Information System (INIS)

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

1991-01-01

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

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

International Nuclear Information System (INIS)

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

2005-01-01

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

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

Directory of Open Access Journals (Sweden)

Venot Olivia

2014-02-01

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

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

Science.gov (United States)

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

2016-01-25

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

Heat stability evaluations of Co/SiO2 multilayers

International Nuclear Information System (INIS)

Ishino, Masahiko; Koike, Masato; Kanehira, Mika; Satou, Futami; Terauchi, Masami; Sano, Kazuo

2008-01-01

The heat stability of Co/SiO 2 multilayers was evaluated. Co/SiO 2 multilayer samples were deposited on Si substrate by means of an ion beam sputtering method, and annealed at temperatures from 100degC to 600degC in a vacuum furnace. For the structural and optical evaluations, small angle x-ray diffraction (XRD) measurements, soft x-ray reflectivity measurements, and transmission electron microscopy (TEM) observations were carried out. As the results, the Co/SiO 2 multilayer samples annealed up to 400degC maintained the initial multilayer structures, and kept almost the same soft x-ray reflectivities as that of the as-deposited Co/SiO 2 multilayer sample. A deterioration of the multilayer structure caused by the growth of Co grains was found on the Co/SiO 2 multilayer samples annealed over 500degC, and the soft x-ray reflectivity dropped in accordance with the deterioration of the multilayer structure. (author)

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

Science.gov (United States)

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

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

Directory of Open Access Journals (Sweden)

Noelia Álvarez-Gutiérrez

2016-03-01

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

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

Directory of Open Access Journals (Sweden)

M. R. Raupach

2014-07-01

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

Reduced tillage and cover crops as a strategy for mitigating atmospheric CO2 increase through soil organic carbon sequestration in dry Mediterranean agroecosystems.

Science.gov (United States)

Almagro, María; Garcia-Franco, Noelia; de Vente, Joris; Boix-Fayos, Carolina; Díaz-Pereira, Elvira; Martínez-Mena, María

2016-04-01

The implementation of sustainable land management (SLM) practices in semiarid Mediterranean agroecosystems can be beneficial to maintain or enhance levels of soil organic carbon and mitigate current atmospheric CO2 increase. In this study, we assess the effects of different tillage treatments (conventional tillage (CT), reduced tillage (RT), reduced tillage combined with green manure (RTG), and no tillage (NT)) on soil CO2 efflux, aggregation and organic carbon stabilization in two semiarid organic rainfed almond (Prunus dulcis Mill., var. Ferragnes) orchards located in SE Spain Soil CO2 efflux, temperature and moisture were measured monthly between May 2012 and December 2014 (site 1), and between February 2013 and December 2014 (site 2). In site 1, soil CO2 efflux rates were also measured immediately following winter and spring tillage operations. Aboveground biomass inputs were estimated at the end of the growing season in each tillage treatment. Soil samples (0-15 cm) were collected in the rows between the trees (n=4) in October 2012. Four aggregate size classes were distinguished by sieving (large and small macroaggregates, free microaggregates, and free silt plus clay fraction), and the microaggregates occluded within macroaggregates (SMm) were isolated. Soil CO2efflux rates in all tillage treatments varied significantly during the year, following changes during the autumn, winter and early spring, or changes in soil moisture during late spring and summer. Repeated measures analyses of variance revealed that there were no significant differences in soil CO2 efflux between tillage treatments throughout the study period at both sites. Average annual values of C lost by soil respiration were slightly but not significantly higher under RT and RTG treatments (492 g C-CO2 m-2 yr-1) than under NT treatment (405 g C-CO2 m-2 yr-1) in site 1, while slightly but not significantly lower values were observed under RT and RTG treatments (468 and 439 g C-CO2 m-2 yr-1

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

Science.gov (United States)

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

2005-08-01

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

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

DEFF Research Database (Denmark)

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

2010-01-01

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

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

Science.gov (United States)

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

2012-12-17

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

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

Science.gov (United States)

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).

Glacial-interglacial atmospheric CO2 change: a possible

Directory of Open Access Journals (Sweden)

L. C. Skinner

2009-09-01

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

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

Science.gov (United States)

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

2013-12-01

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

Power stabilized CO2 gas transport laser

International Nuclear Information System (INIS)

Foster, J.D.; Kirk, R.F.; Moreno, F.E.; Ahmed, S.A.

1975-01-01

The output power of a high power (1 kW or more) CO 2 gas transport laser is stabilized by flowing the gas mixture over copper plated baffles in the gas channel during operation of the laser. Several other metals may be used instead of copper, for example, nickel, manganese, palladium, platinum, silver and gold. The presence of copper in the laser gas circuit stabilizes output power by what is believed to be a compensation of the chemical changes in the gas due to the cracking action of the electrical discharge which has the effect of diminishing the capactiy of the carbon dioxide gas mixture to maintain the rated power output of the laser. (U.S.)

Regional scale variations of atmospheric CO2 and CH4 from satellite observation

International Nuclear Information System (INIS)

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

2014-01-01

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

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

Science.gov (United States)

Opdyke, B N; Walker, J C

1992-08-01

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

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

Energy Technology Data Exchange (ETDEWEB)

Revelle, R; Suess, H E

1957-01-01

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

High temperature stability of surfactant capped CoFe2O4 nanoparticles

International Nuclear Information System (INIS)

Ayyappan, S.; Panneerselvam, G.; Antony, M.P.; Philip, John

2011-01-01

Highlights: → Self-assembled molecular layers of surfactant on nanoparticles are often used to modify surface properties. → We demonstrate that a surfactant nanolayer on CoFe 2 O 4 nanoparticles can act as a strong reducing agent under high temperature vacuum annealing. → We propose a possible reduction mechanism of CoFe 2 O 4 nanoparticles under air and vacuum annealing. → Our results are important in the understanding of the stability of nanoparticles at high temperatures. - Abstract: We investigate the effect of adsorbed surfactant on the structural stability of CoFe 2 O 4 nanoparticles during vacuum thermal annealing. In-situ high temperature X-ray diffraction studies show a reduction of oleic acid coated CoFe 2 O 4 nanoparticles into α-Fe and CoO under annealing at 800 deg. C. On the contrary, the uncoated CoFe 2 O 4 nanoparticles remains stable, with its cubic phase intact, even at 1000 deg. C. Thermo-gravimetric analysis coupled mass spectra reveals that the evolved carbon from the surfactant aids the removal of oxygen atom from CoFe 2 O 4 lattice thereby reducing it to α-Fe and CoO phases. These results are important in tailoring stable CoFe 2 O 4 nanostructures for various applications.

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

Energy Technology Data Exchange (ETDEWEB)

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

2015-10-15

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

Towards CO2 sequestration and applications of CO2 hydrates: the effects of tetrahydrofuran on the phase equilibria of CO2 hydrates

International Nuclear Information System (INIS)

Khalik, M.S.; Peters, C.J.

2006-01-01

The increasing quantity of carbon dioxide (CO 2 ) in the atmosphere has caused widespread global concerns. Capturing CO 2 from its sources and stored it in the form of gas hydrates and application of CO 2 hydrates are among the proposed methods to overcome this problem. In order to make hydrate-based process more attractive, the use of cyclic ethers as promoters is suggested to reduce the required hydrate formation pressure and enhancing the corresponding kinetic rate. In the present work, tetrahydrofuran (THF) is chosen as a hydrate promoter, participating in forming hydrates and produces mixed hydrate together with CO 2 . The pressure and temperature ranges of hydrate stability region are carefully determined through phase equilibrium measurement of the ternary CO 2 , tetrahydrofuran (THF) and water systems. From the experimental results, it is confirmed that the presence of THF in CO 2 + water systems will extend the hydrate formation region to higher temperature at a constant pressure. The extension of the hydrate stability region is depended on the overall concentration of the ternary system. Moreover, four-phase equilibrium of H-Lw-Lv-V is observed in the system, which may be due to a liquid phase split. In the region where the four-phase equilibrium exists, the ternary system loses its concentration dependency of the hydrate equilibrium conditions. (Author)

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

NARCIS (Netherlands)

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

2013-01-01

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

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

International Nuclear Information System (INIS)

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

2015-01-01

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

Sustained effects of atmospheric [CO2] and nitrogen availability on forest soil CO2 efflux.

Science.gov (United States)

Oishi, A Christopher; Palmroth, Sari; Johnsen, Kurt H; McCarthy, Heather R; Oren, Ram

2014-04-01

Soil CO2 efflux (Fsoil ) is the largest source of carbon from forests and reflects primary productivity as well as how carbon is allocated within forest ecosystems. Through early stages of stand development, both elevated [CO2] and availability of soil nitrogen (N; sum of mineralization, deposition, and fixation) have been shown to increase gross primary productivity, but the long-term effects of these factors on Fsoil are less clear. Expanding on previous studies at the Duke Free-Air CO2 Enrichment (FACE) site, we quantified the effects of elevated [CO2] and N fertilization on Fsoil using daily measurements from automated chambers over 10 years. Consistent with previous results, compared to ambient unfertilized plots, annual Fsoil increased under elevated [CO2] (ca. 17%) and decreased with N (ca. 21%). N fertilization under elevated [CO2] reduced Fsoil to values similar to untreated plots. Over the study period, base respiration rates increased with leaf productivity, but declined after productivity saturated. Despite treatment-induced differences in aboveground biomass, soil temperature and water content were similar among treatments. Interannually, low soil water content decreased annual Fsoil from potential values - estimated based on temperature alone assuming nonlimiting soil water content - by ca. 0.7% per 1.0% reduction in relative extractable water. This effect was only slightly ameliorated by elevated [CO2]. Variability in soil N availability among plots accounted for the spatial variability in Fsoil , showing a decrease of ca. 114 g C m(-2) yr(-1) per 1 g m(-2) increase in soil N availability, with consistently higher Fsoil in elevated [CO2] plots ca. 127 g C per 100 ppm [CO2] over the +200 ppm enrichment. Altogether, reflecting increased belowground carbon partitioning in response to greater plant nutritional needs, the effects of elevated [CO2] and N fertilization on Fsoil in this stand are sustained beyond the early stages of stand development and

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

OpenAIRE

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

1994-01-01

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

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

Science.gov (United States)

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.

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

Science.gov (United States)

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.

Interfacing a one-dimensional lake model with a single-column atmospheric model: 2. Thermal response of the deep Lake Geneva, Switzerland under a 2 × CO2 global climate change

Science.gov (United States)

Perroud, Marjorie; Goyette, StéPhane

2012-06-01

In the companion to the present paper, the one-dimensional k-ɛ lake model SIMSTRAT is coupled to a single-column atmospheric model, nicknamed FIZC, and an application of the coupled model to the deep Lake Geneva, Switzerland, is described. In this paper, the response of Lake Geneva to global warming caused by an increase in atmospheric carbon dioxide concentration (i.e., 2 × CO2) is investigated. Coupling the models allowed for feedbacks between the lake surface and the atmosphere and produced changes in atmospheric moisture and cloud cover that further modified the downward radiation fluxes. The time evolution of atmospheric variables as well as those of the lake's thermal profile could be reproduced realistically by devising a set of adjustable parameters. In a "control" 1 × CO2 climate experiment, the coupled FIZC-SIMSTRAT model demonstrated genuine skills in reproducing epilimnetic and hypolimnetic temperatures, with annual mean errors and standard deviations of 0.25°C ± 0.25°C and 0.3°C ± 0.15°C, respectively. Doubling the CO2 concentration induced an atmospheric warming that impacted the lake's thermal structure, increasing the stability of the water column and extending the stratified period by 3 weeks. Epilimnetic temperatures were seen to increase by 2.6°C to 4.2°C, while hypolimnion temperatures increased by 2.2°C. Climate change modified components of the surface energy budget through changes mainly in air temperature, moisture, and cloud cover. During summer, reduced cloud cover resulted in an increase in the annual net solar radiation budget. A larger water vapor deficit at the air-water interface induced a cooling effect in the lake.

An Atmospheric CO2 Record Across the End-Cretaceous Extinction

Science.gov (United States)

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, 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.

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

Science.gov (United States)

Sionit, Nasser; Patterson, David T

1984-12-01

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

CO2 Reforming of CH4 by Atmospheric Pressure Abnormal Glow Plasma

International Nuclear Information System (INIS)

Chen Qi; Dai Wei; Tao Xumei; Yu Hui; Dai Xiaoyan; Yin Yongxiang

2006-01-01

A novel plasma atmospheric pressure abnormal glow discharge was used to investigate synthesis gas production from reforming methane and carbon dioxide. Special attentions were paid to the discharge characteristics and CH 4 , CO 2 conversion, H 2 , CO selectivity, and ratio of H 2 /CO varied with the changing of discharging power, the total flux, and the ratio of CH 4 /CO 2 . Experiments were performed in wider operation variables, the discharging power of 240 to 600 W, the CH 4 /CO 2 of 0.2 to 1.0 and the total flux of 140 to 500 mL/min. The experiments showed that the conversion of CH 4 and CO 2 was up to 91.9% and 83.2%, the selectivity of CO and H 2 was also up to 80% and 90% and H 2 /CO mole ratio was 0.2 to 1.2, respectively. A brief analysis for discharge characteristics and the experimental results were given

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

Science.gov (United States)

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

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

Science.gov (United States)

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

2004-05-01

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

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

Science.gov (United States)

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

CO2 Capture and Reuse

International Nuclear Information System (INIS)

Thambimuthu, K.; Gupta, M.; Davison, J.

2003-01-01

CO2 capture and storage including its utilization or reuse presents an opportunity to achieve deep reductions in greenhouse gas emissions from fossil energy use. The development and deployment of this option could significantly assist in meeting a future goal of achieving stabilization of the presently rising atmospheric concentration of greenhouse gases. CO2 capture from process streams is an established concept that has achieved industrial practice. Examples of current applications include the use of primarily, solvent based capture technologies for the recovery of pure CO2 streams for chemical synthesis, for utilization as a food additive, for use as a miscible agent in enhanced oil recovery operations and removal of CO2 as an undesired contaminant from gaseous process streams for the production of fuel gases such as hydrogen and methane. In these applications, the technologies deployed for CO2 capture have focused on gas separation from high purity, high pressure streams and in reducing (or oxygen deficient) environments, where the energy penalties and cost for capture are moderately low. However, application of the same capture technologies for large scale abatement of greenhouse gas emissions from fossil fuel use poses significant challenges in achieving (at comparably low energy penalty and cost) gas separation in large volume, dilute concentration and/or low pressure flue gas streams. This paper will focus on a review of existing commercial methods of CO2 capture and the technology stretch, process integration and energy system pathways needed for their large scale deployment in fossil fueled processes. The assessment of potential capture technologies for the latter purpose will also be based on published literature data that are both 'transparent' and 'systematic' in their evaluation of the overall cost and energy penalties of CO2 capture. In view of the of the fact that many of the existing commercial processes for CO2 capture have seen applications in

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

Science.gov (United States)

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...

Thermal stability, swelling behavior and CO 2 absorption properties of Nanoscale Ionic Materials (NIMs)

KAUST Repository

Andrew Lin, Kun-Yi

2014-11-11

© The Royal Society of Chemistry 2015. Nanoscale Ionic Materials (NIMs) consist of a nanoscale core, a corona of charged brushes tethered on the surface of the core, and a canopy of the oppositely charged species linked to the corona. Unlike conventional polymeric nanocomposites, NIMs can display liquid-like behavior in the absence of solvents, have a negligible vapor pressure and exhibit unique solvation properties. These features enable NIMs to be a promising CO2 capture material. To optimize NIMs for CO2 capture, their structure-property relationships were examined by investigating the roles of the canopy and the core in their thermal stability, and thermally- and CO2-induced swelling behaviors. NIMs with different canopy sizes and core fractions were synthesized and their thermal stability as well as thermally- and CO2-induced swelling behaviors were determined using thermogravimetry, and ATR FT-IR and Raman spectroscopies. It was found that the ionic bonds between the canopy and the corona, as well as covalent bonds between the corona and the core significantly improved the thermal stability compared to pure polymer and polymer/nanofiller mixtures. A smaller canopy size and a larger core fraction led to a greater enhancement in thermal stability. This thermal stability enhancement was responsible for the long-term thermal stability of NIMs over 100 temperature swing cycles. Owing to their ordered structure, NIMs swelled less when heated or when they adsorbed CO2 compared to their corresponding polymers. This journal is

Thermal stability, swelling behavior and CO 2 absorption properties of Nanoscale Ionic Materials (NIMs)

KAUST Repository

Andrew Lin, Kun-Yi; Park, Youngjune; Petit, Camille; Park, Ah-Hyung Alissa

2014-01-01

© The Royal Society of Chemistry 2015. Nanoscale Ionic Materials (NIMs) consist of a nanoscale core, a corona of charged brushes tethered on the surface of the core, and a canopy of the oppositely charged species linked to the corona. Unlike conventional polymeric nanocomposites, NIMs can display liquid-like behavior in the absence of solvents, have a negligible vapor pressure and exhibit unique solvation properties. These features enable NIMs to be a promising CO2 capture material. To optimize NIMs for CO2 capture, their structure-property relationships were examined by investigating the roles of the canopy and the core in their thermal stability, and thermally- and CO2-induced swelling behaviors. NIMs with different canopy sizes and core fractions were synthesized and their thermal stability as well as thermally- and CO2-induced swelling behaviors were determined using thermogravimetry, and ATR FT-IR and Raman spectroscopies. It was found that the ionic bonds between the canopy and the corona, as well as covalent bonds between the corona and the core significantly improved the thermal stability compared to pure polymer and polymer/nanofiller mixtures. A smaller canopy size and a larger core fraction led to a greater enhancement in thermal stability. This thermal stability enhancement was responsible for the long-term thermal stability of NIMs over 100 temperature swing cycles. Owing to their ordered structure, NIMs swelled less when heated or when they adsorbed CO2 compared to their corresponding polymers. This journal is

Area 2. Use Of Engineered Nanoparticle-Stabilized CO₂ Foams To Improve Volumetric Sweep Of CO₂ EOR Processes

Energy Technology Data Exchange (ETDEWEB)

DiCarlo, David [Univ. of Texas, Austin, TX (United States); Huh, Chun [Univ. of Texas, Austin, TX (United States); Johnston, Keith P. [Univ. of Texas, Austin, TX (United States)

2015-01-31

The goal of this project was to develop a new CO₂ injection enhanced oil recovery (CO₂-EOR) process using engineered nanoparticles with optimized surface coatings that has better volumetric sweep efficiency and a wider application range than conventional CO₂-EOR processes. The main objectives of this project were to (1) identify the characteristics of the optimal nanoparticles that generate extremely stable CO₂ foams in situ in reservoir regions without oil; (2) develop a novel method of mobility control using “self-guiding” foams with smart nanoparticles; and (3) extend the applicability of the new method to reservoirs having a wide range of salinity, temperatures, and heterogeneity. Concurrent with our experimental effort to understand the foam generation and transport processes and foam-induced mobility reduction, we also developed mathematical models to explain the underlying processes and mechanisms that govern the fate of nanoparticle-stabilized CO₂ foams in porous media and applied these models to (1) simulate the results of foam generation and transport experiments conducted in beadpack and sandstone core systems, (2) analyze CO₂ injection data received from a field operator, and (3) aid with the design of a foam injection pilot test. Our simulator is applicable to near-injection well field-scale foam injection problems and accounts for the effects due to layered heterogeneity in permeability field, foam stabilizing agents effects, oil presence, and shear-thinning on the generation and transport of nanoparticle-stabilized C/W foams. This report presents the details of our experimental and numerical modeling work and outlines the highlights of our findings.

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

International Nuclear Information System (INIS)

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

2004-01-01

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

Mars - CO2 adsorption and capillary condensation on clays: Significance for volatile storage and atmospheric history

Science.gov (United States)

Fanale, F. P.; Cannon, W. A.

1979-01-01

Results on the adsorbate-adsorbent system CO2-nontronite are reported at 230, 196, and 158 deg K, covering the range of subsurface regolith temperature on Mars. A three-part regolith-atmosphere-cap model reveals that cold nontronite, and expanding clays in general, are far better but far more complex CO2 adsorbers than cold pulverized basalt. In addition, the layered terrain, and possibly the adjacent debris mantle, contains about 2% or more by mass of atmosphere-exchangeable CO2 and the total regolith inventory of available adsorbed CO2 is estimated to be 400 g/ sq cm.

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

Science.gov (United States)

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

2017-10-13

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

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

Science.gov (United States)

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 (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.

Formation reactions and thermal stability of Ca/sub 2/NbCoO/sub 6/ and Ca/sub 2/TaCoO/sub 6/

Energy Technology Data Exchange (ETDEWEB)

Kuleshova, T B; Razumovskaya, O N; Belyaev, I N; Salei, V S [Rostovskij-na-Donu Gosudarstvennyj Univ. (USSR)

1979-11-01

Ca/sub 2/M/sup 5/CoO/sub 6/ compounds and reactions of their formation from oxides were investigated by thermogravimetric and X-ray phase analysis methods. Optimum conditions for synthesizing the above compounds have been found, and the degree of oxidation of Co therein, determined. The thermal stability of the compounds was also studied. It was shown, that the stability of Co (3) in Ca/sub 2/NbCaO/sub 6/ Ca/sub 2/TaCoO/sub 6/ is higher than that in similar compounds containing Pb. The resultant compounds are pure perovskites. Presented are the calculated and the experimental values of perovskite cell parameters.

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

Science.gov (United States)

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

Tailings and mineral carbonation : the potential for atmospheric CO{sub 2} sequestration

Energy Technology Data Exchange (ETDEWEB)

Rollo, H.A. [Lorax Environmental Services Ltd., Vancouver, BC (Canada); Jamieson, H.E. [Queen' s Univ., Kingston, ON (Canada). Dept. of Geological Sciences and Geological Engineering; Lee, C.A. [Dillon Consulting Ltd., Cambridge, ON (Canada)

2009-02-15

Carbon dioxide (CO{sub 2}) sequestration includes geological storage, ocean storage, organic storage, and mineral storage (mineral carbonation). This presentation discussed tailings and mineral carbonation and the potential for atmospheric CO{sub 2} sequestration. In particular, it outlined CO{sub 2} sequestration and presented a history of investigations. The Ekati Diamond Mine was discussed with particular reference to its location, geology, and processing. Other topics that were presented included mineralogy; water chemistry; modeling results; and estimates of annual CO{sub 2} sequestration. Conclusions and implications were also presented. It was concluded that ore processing at mines with ultramafic host rocks have the potential to partially offset CO{sub 2} emissions. In addition, it was found that existing tailings at ultramafic deposits may be viable source materials for CO{sub 2} sequestration by mineral carbonation. tabs., figs.

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

Science.gov (United States)

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.

Does Silicate Weathering of Loess Affect Atmospheric CO2?

Science.gov (United States)

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

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

Energy Technology Data Exchange (ETDEWEB)

Oechel, W.C.

1992-04-01

Northern ecosystems contain up to 455 Gt of C in the soil active layer and upper permafrost. The soil carbon in these layers is equivalent to approximately 60% of the carbon currently in the atmosphere as CO{sub 2}. Much of this carbon is stored in the soil as dead organic matter. Its fate is subject to the net effects of global change on the plant and soil systems of northern ecosystems. The arctic alone contains about 60 Gt C, 90% of which is present in the soil active layer and upper permafrost. The arctic is assumed to have been a sink for CO{sub 2} during the historic and recent geologic past. The arctic has the potential to be a very large, long-term source or sink of CO{sub 2} with respect to the atmosphere. In situ experimental manipulations of atmospheric CO{sub 2}, indicated that there is little effect of elevated atmospheric CO{sub 2} on leaf level photosynthesis or whole-ecosystem CO{sub 2} flux over the course of weeks to years, respectively. However, there may be longer- term ecosystem responses to elevated CO{sub 2} that could ultimately affect ecosystem CO{sub 2} balance. In addition to atmospheric CO{sub 2}, climate may affect net ecosystem carbon balance. Recent results indicate that the arctic has become a source of CO{sub 2} to the atmosphere. This change coincides with recent climatic variation in the arctic, and suggests a positive feedback of arctic ecosystems on atmospheric CO{sub 2} and global change. The research proposed in this application has four principal aspects: (A) Long-term response of arctic plants and ecosystems to elevated atmospheric CO{sub 2}; (B) Circumpolar patterns of net ecosystem CO{sub 2} flux; (C) In situ controls by temperature and moisture on net ecosystem CO{sub 2} flux; (D) Scaling of CO{sub 2} flux from plot, to landscape, to regional scales (In conjunction with research proposed for NSF support).

Dispersive infrared spectroscopy measurements of atmospheric CO2 using a Fabry–Pérot interferometer sensor

International Nuclear Information System (INIS)

Chan, K.L.; Ning, Z.; Westerdahl, D.; Wong, K.C.; Sun, Y.W.; Hartl, A.; Wenig, M.O.

2014-01-01

In this paper, we present the first dispersive infrared spectroscopic (DIRS) measurement of atmospheric carbon dioxide (CO 2 ) using a new scanning Fabry–Pérot interferometer (FPI) sensor. The sensor measures the optical spectra in the mid infrared (3900 nm to 5220 nm) wavelength range with full width half maximum (FWHM) spectral resolution of 78.8 nm at the CO 2 absorption band (∼ 4280 nm) and sampling resolution of 20 nm. The CO 2 concentration is determined from the measured optical absorption spectra by fitting it to the CO 2 reference spectrum. Interference from other major absorbers in the same wavelength range, e.g., carbon monoxide (CO) and water vapor (H 2 O), was taken out by including their reference spectra in the fit as well. The detailed descriptions of the instrumental setup, the retrieval procedure, a modeling study for error analysis as well as laboratory validation using standard gas concentrations are presented. An iterative algorithm to account for the non-linear response of the fit function to the absorption cross sections due to the broad instrument function was developed and tested. A modeling study of the retrieval algorithm showed that errors due to instrument noise can be considerably reduced by using the dispersive spectral information in the retrieval. The mean measurement error of the prototype DIRS CO 2 measurement for 1 minute averaged data is about ± 2.5 ppmv, and down to ± 0.8 ppmv for 10 minute averaged data. A field test of atmospheric CO 2 measurements were carried out in an urban site in Hong Kong for a month and compared to a commercial non-dispersive infrared (NDIR) CO 2 analyzer. 10 minute averaged data shows good agreement between the DIRS and NDIR measurements with Pearson correlation coefficient (R) of 0.99. This new method offers an alternative approach of atmospheric CO 2 measurement featuring high accuracy, correction of non-linear absorption and interference of water vapor. - Highlights: • Dispersive infrared

Changes in vegetation phenology are not reflected in atmospheric CO2 and 13 C/12 C seasonality.

Science.gov (United States)

Gonsamo, Alemu; D'Odorico, Petra; Chen, Jing M; Wu, Chaoyang; Buchmann, Nina

2017-10-01

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, CO 2 uptake through photosynthesis and release through respiration, determine the influence of the terrestrial ecosystem on the atmospheric CO 2 and 13 C/ 12 C seasonality. Here, we use four CO 2 observation stations in the Northern Hemisphere, namely Alert, La Jolla, Point Barrow, and Mauna Loa Observatory, to determine how changes in vegetation productivity and phenology, respiration, and air temperature affect both the atmospheric CO 2 and 13 C/ 12 C seasonality. Since the 1960s, the only significant long-term trend of CO 2 and 13 C/ 12 C seasonality was observed at the northern most station, Alert, where the spring CO 2 drawdown dates advanced by 0.65 ± 0.55 days yr -1 , contributing to a nonsignificant increase in length of the CO 2 uptake period (0.74 ± 0.67 days yr -1 ). For Point Barrow station, vegetation phenology changes in well-watered ecosystems such as the Canadian and western Siberian wetlands contributed the most to 13 C/ 12 C seasonality while the CO 2 seasonality was primarily linked to nontree vegetation. Our results indicate significant increase in the Northern Hemisphere soil respiration. This means, increased respiration of 13 C depleted plant materials cancels out the 12 C gain from enhanced vegetation activities during the start and end of growing season. These findings suggest therefore that parallel warming-induced increases both in photosynthesis and respiration contribute to the long-term stability of CO 2 and 13 C/ 12 C seasonality under changing climate and vegetation activity. The summer photosynthesis and the soil respiration in the dormant seasons have become more vigorous which lead to increased peak-to-through CO 2 amplitude. As the relative magnitude of the increased

Pollutants transport and atmospheric variability of CO2 over Siberia: contribution of airborne measurements

International Nuclear Information System (INIS)

Paris, J.D.

2008-12-01

The work presented here intends to characterize the variations of atmospheric concentrations of CO 2 , CO, O 3 and ultrafine particles, over a large scale aircraft transect above Siberia, during three intensive YAK-AEROSIB campaigns in April 2006, September 2006 and August 2007, respectively. Pollutant and greenhouse gases distribution in this poorly studied region is needed to model atmospheric long range transport. I show here that CO concentrations at the time of the campaigns is broadly affected by (1) advection of Chinese pollutants through baro-clinic perturbations, (2) advection (diffuse or not) of European pollutants at various altitudes, (3) and of biomass burning from Central Asia. This set of factors is analyzed through a novel statistical technique based on clustering of backward transport simulated by the FLEXPART Lagrangian model. Large observed CO 2 gradients in summer are matched against vertical mixing in GCM simulated CO 2 . At last I present ultrafine particle measurements, and a possible nucleation summer maximum in the clean, continental mid-troposphere. (author)

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

Science.gov (United States)

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.

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

Science.gov (United States)

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

1978-01-01

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

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

International Nuclear Information System (INIS)

Stuiver, M.; Quay, P.D.

1981-01-01

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

Enhanced priming of old, not new soil carbon at elevated atmospheric CO2

DEFF Research Database (Denmark)

Vestergard, Mette; Reinsch, Sabine; Bengtson, Per

2016-01-01

Rising atmospheric CO2 concentrations accompanied by global warming and altered precipitation patterns calls for assessment of long-term effects of these global changes on carbon (C) dynamics in terrestrial ecosystems, as changes in net C exchange between soil and atmosphere will impact the atmos......Rising atmospheric CO2 concentrations accompanied by global warming and altered precipitation patterns calls for assessment of long-term effects of these global changes on carbon (C) dynamics in terrestrial ecosystems, as changes in net C exchange between soil and atmosphere will impact...... accelerate the decomposition of soil organic C (SOC), a phenomenon termed ‘the priming effect’, and the priming effect is most pronounced at low soil N availability. Hence, we hypothesized that priming of SOC decomposition in response to labile C addition would increase in soil exposed to long-term elevated...... decomposition of relatively old SOC fractions, i.e. SOC assimilated more than 8 years before sampling....

Theoretical UV absorption spectra of hydrodynamically escaping O2/CO2-rich exoplanetary atmospheres

International Nuclear Information System (INIS)

Gronoff, G.; Mertens, C. J.; Norman, R. B.; Maggiolo, R.; Wedlund, C. Simon; Bell, J.; Bernard, D.; Parkinson, C. J.; Vidal-Madjar, A.

2014-01-01

Characterizing Earth- and Venus-like exoplanets' atmospheres to determine if they are habitable and how they are evolving (e.g., equilibrium or strong erosion) is a challenge. For that endeavor, a key element is the retrieval of the exospheric temperature, which is a marker of some of the processes occurring in the lower layers and controls a large part of the atmospheric escape. We describe a method to determine the exospheric temperature of an O 2 - and/or CO 2 -rich transiting exoplanet, and we simulate the respective spectra of such a planet in hydrostatic equilibrium and hydrodynamic escape. The observation of hydrodynamically escaping atmospheres in young planets may help constrain and improve our understanding of the evolution of the solar system's terrestrial planets' atmospheres. We use the dependency of the absorption spectra of the O 2 and CO 2 molecules on the temperature to estimate the temperature independently of the total absorption of the planet. Combining two observables (two parts of the UV spectra that have a different temperature dependency) with the model, we are able to determine the thermospheric density profile and temperature. If the slope of the density profile is inconsistent with the temperature, then we infer the hydrodynamic escape. We address the question of the possible biases in the application of the method to future observations, and we show that the flare activity should be cautiously monitored to avoid large biases.

Relationship between synoptic scale weather systems and column averaged atmospheric CO2

Science.gov (United States)

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

2005-12-01

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

Stability of lamb loin stored under refrigeration and packed in different modified atmosphere packaging systems.

Science.gov (United States)

Fernandes, Rafaella de Paula Paseto; Freire, Maria Teresa de Alvarenga; de Paula, Elisa Silva Maluf; Kanashiro, Ana Livea Sayuri; Catunda, Fernanda Antunes Pinto; Rosa, Alessandra Fernandes; Balieiro, Júlio Cesar de Carvalho; Trindade, Marco Antonio

2014-01-01

The aim of the present study was to evaluate the effect of different modified atmosphere packaging (MAP) systems (vacuum, 75% O2+25% CO2 and 100% CO2) on the stability of lamb loins stored at 1±1°C for 28 days. Microbiological (counts of aerobic and anaerobic psychrotrophic microorganisms, coliform at 45°C, coagulase-positive staphylococci and lactic acid bacteria and presence of Salmonella), physical and chemical (thiobarbituric acid reactive substances [TBARS], objective color, pH, water loss from cooking [WLC] and shear force), sensory (acceptance testing using a 9-point hedonic scale) and gas composition analyses were performed. Lamb meat remained stable with respect to the majority of the evaluated physical and chemical indexes and within the standards established by Brazilian legislation for pathogenic microorganisms throughout the storage period in all three packaging systems. However, with respect to psychrotrophic microorganisms, 100% CO2 packaging system provided increased stability despite presenting lower appearance preference. © 2013.

Influence of Metal Transfer Stability and Shielding Gas Composition on CO and CO2 Emissions during Short-circuiting MIG/MAG Welding

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Valter Alves de Meneses

Full Text Available Abstract: Several studies have demonstrated the influence of parameters and shielding gas on metal transfer stability or on the generation of fumes in MIG/MAG welding, but little or nothing has been discussed regarding the emission of toxic and asphyxiating gases, particularly as it pertains to parameterization of the process. The purpose of this study was to analyze and evaluate the effect of manufacturing aspects of welding processes (short-circuit metal transfer stability and shielding gas composition on the gas emission levels during MIG/MAG welding (occupational health and environmental aspects. Using mixtures of Argon with CO2 and O2 and maintaining the same average current and the same weld bead volume, short-circuit welding was performed with carbon steel welding wire in open (welder’s breathing zone and confined environments. The welding voltage was adjusted to gradually vary the transfer stability. It was found that the richer the composition of the shielding gas is in CO2, the more CO and CO2 are generated by the arc. However, unlike fume emission, voltage and transfer stability had no effect on the generation of these gases. It was also found that despite the large quantity of CO and CO2 emitted by the arc, especially when using pure CO2 shielding gas, there was no high level residual concentration of CO and CO2 in or near the worker’s breathing zone, even in confined work cells.

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

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S. L. Heck

2012-02-01

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

Error characterization of CO2 vertical mixing in the atmospheric transport model WRF-VPRM

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U. Karstens

2012-03-01

Full Text Available One of the dominant uncertainties in inverse estimates of regional CO2 surface-atmosphere fluxes is related to model errors in vertical transport within the planetary boundary layer (PBL. In this study we present the results from a synthetic experiment using the atmospheric model WRF-VPRM to realistically simulate transport of CO2 for large parts of the European continent at 10 km spatial resolution. To elucidate the impact of vertical mixing error on modeled CO2 mixing ratios we simulated a month during the growing season (August 2006 with different commonly used parameterizations of the PBL (Mellor-Yamada-Janjić (MYJ and Yonsei-University (YSU scheme. To isolate the effect of transport errors we prescribed the same CO2 surface fluxes for both simulations. Differences in simulated CO2 mixing ratios (model bias were on the order of 3 ppm during daytime with larger values at night. We present a simple method to reduce this bias by 70–80% when the true height of the mixed layer is known.

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

Science.gov (United States)

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 0.7), 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

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

Science.gov (United States)

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.

Climate change and agroecosystems: the effect of elevated atmospheric CO2 and temperature on crop growth, development, and yield

Directory of Open Access Journals (Sweden)

Streck Nereu Augusto

2005-01-01

Full Text Available The amount of carbon dioxide (CO2 of the Earths atmosphere is increasing, which has the potential of increasing greenhouse effect and air temperature in the future. Plants respond to environment CO2 and temperature. Therefore, climate change may affect agriculture. The purpose of this paper was to review the literature about the impact of a possible increase in atmospheric CO2 concentration and temperature on crop growth, development, and yield. Increasing CO2 concentration increases crop yield once the substrate for photosynthesis and the gradient of CO2 concentration between atmosphere and leaf increase. C3 plants will benefit more than C4 plants at elevated CO2. However, if global warming will take place, an increase in temperature may offset the benefits of increasing CO2 on crop yield.

Atmospheric pCO2 Reconstructed across the Early Eocene Hyperthermals

Science.gov (United States)

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.

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

Science.gov (United States)

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...

Ignition and devolatilization of pulverized coals in lower oxygen content O{sub 2}/CO{sub 2} atmosphere

Energy Technology Data Exchange (ETDEWEB)

Huang, Xiaohong; Li, Jing; Liu, Zhaohui; Yang, Ming; Wang, Dingbang; Zheng, Chuguang [Huazhong Univ. of Science and Technology, Wuhan (China). State Key Lab. of Coal Combustion

2013-07-01

High speed camera is employed to capture the transient images of the burning particle in a flat-flame entrained flow reactor, some information of the burning particle, such as the optical intensity and the residence time, are obtained through analysis of transient images. The ignition and devolatilization behavior of different rank coals at 1,670, 1,770 and 1,940 K over a range of 2-30% O{sub 2} in both N{sub 2} and CO{sub 2} diluent gases are researched. The results indicate that the laws of ignition and devolatilization of pulverized coals in low oxygen O{sub 2}/CO{sub 2} atmosphere are consistent with the literature, which focus on the environments of high oxygen contents (10-30%) or lower temperate (900-1,500 K). With the gas temperature and oxygen content increased, the ignition delay time and devolatilization time for the lower oxygen content cases decreased for both N{sub 2} and CO{sub 2} atmosphere. With the use CO{sub 2} in place of N{sub 2} in low oxygen content, the ignition delay was retarded and the duration of devolatilization was increased. The effect of CO{sub 2} on coal particle ignition is explained by its higher molar specific heat. And the effect of CO{sub 2} on devolatilization results from its effect on the diffusion rates of volatile fuel and oxygen.

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

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P. Peylin

2013-10-01

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

Comparative Analysis of Alternative Spectral Bands of CO2 and O2 for the Sensing of CO2 Mixing Ratios

Science.gov (United States)

Pliutau, Denis; Prasad, Narasimha S.

2013-01-01

We performed comparative studies to establish favorable spectral regions and measurement wavelength combinations in alternative bands of CO2 and O2, for the sensing of CO2 mixing ratios (XCO2) in missions such as ASCENDS. The analysis employed several simulation approaches including separate layers calculations based on pre-analyzed atmospheric data from the modern-era retrospective analysis for research and applications (MERRA), and the line-byline radiative transfer model (LBLRTM) to obtain achievable accuracy estimates as a function of altitude and for the total path over an annual span of variations in atmospheric parameters. Separate layer error estimates also allowed investigation of the uncertainties in the weighting functions at varying altitudes and atmospheric conditions. The parameters influencing the measurement accuracy were analyzed independently and included temperature sensitivity, water vapor interferences, selection of favorable weighting functions, excitations wavelength stabilities and other factors. The results were used to identify favorable spectral regions and combinations of on / off line wavelengths leading to reductions in interferences and the improved total accuracy.

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

Energy Technology Data Exchange (ETDEWEB)

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

1996-12-31

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

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

Energy Technology Data Exchange (ETDEWEB)

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

1995-12-31

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

Organic chemistry in a CO2 rich early Earth atmosphere

Science.gov (United States)

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.

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

Science.gov (United States)

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...

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

Science.gov (United States)

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.

Plume spread and atmospheric stability

Energy Technology Data Exchange (ETDEWEB)

Weber, R O [Paul Scherrer Inst. (PSI), Villigen (Switzerland)

1999-08-01

The horizontal spread of a plume in atmospheric dispersion can be described by the standard deviation of horizontal direction. The widely used Pasquill-Gifford classes of atmospheric stability have assigned typical values of the standard deviation of horizontal wind direction and of the lapse rate. A measured lapse rate can thus be used to estimate the standard deviation of wind direction. It is examined by means of a large dataset of fast wind measurements how good these estimates are. (author) 1 fig., 2 refs.

Energy intensity decline implications for stabilization of atmospheric CO2 content

International Nuclear Information System (INIS)

Lightfoot, H.D.; Green, C.

2002-01-01

By calculating the amount of carbon-free energy required to stabilize the level of carbon dioxide in the atmosphere at some level, such as 550 parts per million by volume (ppmv) in 2100, the authors estimate the appropriate rate of world average annual energy intensity decline. The roles played by energy efficiency and long term sectoral changes like shifts in economic activity from high energy intensity sectors or industries to low energy intensity sectors or industries are distinguished. Advances in technology and better and improved procedures, as well as a broader adoption of more efficient technologies currently available are included in the improvements made in energy efficiency. The objective was, for the period 1990 to 2100 (110 years), to estimate the potential energy efficiency increase for world electricity generation. It is noted that electricity generation represents 38 per cent of world energy consumption in 1995, while transportation accounts for 19 per cent and residential, industrial and commercial uses account for 43 per cent. In 2100, it is expected that the overall average decline in energy intensity will be 40.1 per cent of that of 1990, according to the results obtained. Looked at from another perspective, it represents an average annual rate of energy intensity decline of 0.83 per cent for 110 years. Between 0.16 and 0.30 per cent could be added to the impact of sectoral changes on the average annual rate of decline in energy intensity, while 0.83 per cent would be attributable to improvements in energy efficiency, as shown by sensitivity analysis. 33 refs., 9 tabs., 1 fig

Mesoporous carbon composite for CO{sub 2} capture

Energy Technology Data Exchange (ETDEWEB)

Hwang, Chih-Chau; Jin, Zhong; Lu, Wei; Sun, Zhengzong; Alemany, Lawrence; Tour, James M. [Rice University, Houston, TX (United States); Lomeda, Jay R.; Flatt, Austen K. [Nalco Company, Naperville, IL (United States)

2012-07-01

Herein we report a carbon based technology that can be used to rapidly adsorb and release CO{sub 2}. CO{sub 2} uptake by the synthesized composites was determined using a gravimetric method at room temperature and atmospheric pressure. 39% polyethylenimine-mesocarbon (PEI-CMK-3) composite had {approx} 12 wt% CO{sub 2} uptake capacity and a 37% polyvinylamine meso-carbon (PVA-CMK-3) composite had {approx} 13 wt% CO{sub 2} uptake capacity. The sorbents were easily regenerated at 75 deg C and exhibit excellent stability over multiple regeneration cycles. CO{sub 2} uptake was equivalent when using 10% CO{sub 2} in 90% CH{sub 4}, C{sub 2}H{sub 6} and C{sub 3}H{sub 9} mixture, underscoring the efficacy for CO{sub 2} separation from natural gas. (author)

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

Science.gov (United States)

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.

In situ X-ray and neutron diffraction of the Ruddlesden–Popper compounds (RE2−xSrx)0.98(Fe0.8Co0.2)1−yMgyO4−δ (RE=La, Pr): Structure and CO2 stability

International Nuclear Information System (INIS)

Chatzichristodoulou, C.; Hauback, B.C.; Hendriksen, P.V.

2013-01-01

The crystal structure of the Ruddlesden–Popper compounds (La 1.0 Sr 1.0 ) 0.98 Fe 0.8 Co 0.2 O 4−δ and (La 1.2 Sr 0.8 ) 0.98 (Fe 0.8 Co 0.2 ) 0.8 Mg 0.2 O 4−δ was investigated at 1000 °C in N 2 (a O2 =1×10 −4 ) by in-situ powder neutron diffraction. In-situ powder X-ray diffraction (PXD) was also employed to investigate the temperature dependence of the lattice parameters of the compounds in air and the oxygen activity dependence of the lattice parameters at 800 °C and 1000 °C. The thermal and chemical expansion coefficients, determined along the two crystallographic directions of the tetragonal unit cell, are highly anisotropic. The equivalent pseudo-cubic thermal and chemical expansion coefficients are in agreement with values determined by dilatometry. The chemical stability in CO 2 containing environments of various Ruddlesden–Popper compounds with chemical formula (RE 2−x Sr x ) 0.98 (Fe 0.8 Co 0.2 ) 1−y Mg y O 4−δ (RE=La, Pr), as well as their stability limit in H 2 /H 2 O=4.5 were also determined by in-situ PXD for x=0.9, 1.0 and y=0, 0.2. - Graphical abstract: Influence of electronic configuration on bond length, lattice parameters and anisotropic thermal and chemical expansion. Highlights: ► The thermal and chemical expansion coefficients are largely anisotropic. ► The expansion of the perovskite layers is constrained along the a direction. ► The studied compositions show remarkable thermodynamic stability upon reduction. ► The thermal and chemical expansion coefficients are lower than related perovskites. ► The investigated materials decompose in CO 2 containing atmospheres

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

Science.gov (United States)

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.

Recent widespread tree growth decline despite increasing atmospheric CO2.

Science.gov (United States)

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

2010-07-21

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

Atmospheric and geological CO2 damage costs in energy scenarios

International Nuclear Information System (INIS)

Smekens, K.E.L.; Van der Zwaan, B.C.C.

2006-05-01

Geological carbon dioxide capture and storage (CCS) is currently seriously considered for addressing, in the near term, the problem of climate change. CCS technology is available today and is expected to become an increasingly affordable CO2 abatement alternative. Whereas the rapidly growing scientific literature on CCS as well as experimental and commercial practice demonstrate the technological and economic feasibility of implementing this clean fossil fuel option on a large scale, relatively little attention has been paid so far to the risks and environmental externalities of geological storage of CO2. This paper assesses the effects of including CCS damage costs in a long-term energy scenario analysis for Europe. An external cost sensitivity analysis is performed with a bottom-up energy technology model that accounts not only for CCS technologies but also for their external costs. Our main conclusion is that in a business-as-usual scenario (i.e. without climate change intervention or externality internalisation), CCS technologies are likely to be deployed at least to some extent, mainly in the power generation sector, given the economic benefits of opportunities such as enhanced coal bed methane, oil and gas recovery. Under a strict climate (CO2 emissions) constraint, CCS technologies are deployed massively. With the simultaneous introduction of both CO2 and CCS taxation in the power sector, designed to internalise the external atmospheric and geological effects of CO2 emissions and storage, respectively, we find that CCS will only be developed if the climate change damage costs are at least of the order of 100 euro/t CO2 or the CO2 storage damage costs not more than a few euro/t CO2. When the internalised climate change damage costs are as high as 67 euro/t CO2, the expensive application of CCS to biomass-fuelled power plants (with negative net CO2 emissions) proves the most effective CCS alternative to reduce CO2 emissions, rather than CCS applied to fossil

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

Science.gov (United States)

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.

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

Science.gov (United States)

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

1999-04-01

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 95years a combination of increasing atmospheric CO2 with historical temperature and precipitation variability causes a 4.2% (4.3Pg C) decrease in total carbon storage of potential vegetation in the conterminous US, with vegetation carbon decreasing by 7.2% (3.2Pg C) and soil organic carbon decreasing by 1.9% (1.1Pg 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 yr1 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% (17.7Pg C

Alternative photocatalysts to TiO2 for the photocatalytic reduction of CO2

Science.gov (United States)

Nikokavoura, Aspasia; Trapalis, Christos

2017-01-01

The increased concentration of CO2 in the atmosphere, originating from the burning of fossil fuels in stationary and mobile sources, is referred as the "Anthropogenic Greenhouse Effect" and constitutes a major environmental concern. The scientific community is highly concerned about the resulting enhancement of the mean atmospheric temperature, so a vast diversity of methods has been applied. Thermochemical, electrochemical, photocatalytic, photoelectrochemical processes, as well as combination of solar electricity generation and water splitting processes have been performed in order to lower the CO2 atmospheric levels. Photocatalytic methods are environmental friendly and succeed in reducing the atmospheric CO2 concentration and producing fuels or/and useful organic compounds at the same time. The most common photocatalysts for the CO2 reduction are the inorganic, the carbon based semiconductors and the hybrids based on semiconductors, which combine stability, low cost and appropriate structure in order to accomplish redox reactions. In this review, inorganic semiconductors such as single-metal oxide, mixed-metal oxides, metal oxide composites, layered double hydroxides (LDHs), salt composites, carbon based semiconductors such as graphene based composites, CNT composites, g-C3N4 composites and hybrid organic-inorganic materials (ZIFs) were studied. TiO2 and Ti based photocatalysts are extensively studied and therefore in this review they are not mentioned.

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

Science.gov (United States)

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...

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

Science.gov (United States)

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

1993-01-01

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

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

Science.gov (United States)

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

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

Science.gov (United States)

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

2016-06-14

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.

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

Science.gov (United States)

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.

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

Science.gov (United States)

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.

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

Directory of Open Access Journals (Sweden)

N. Towles

2015-07-01

Full Text Available 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.

Nb-TiO{sub 2}/polymer hybrid solar cells with photovoltaic response under inert atmosphere conditions

Energy Technology Data Exchange (ETDEWEB)

Lira-Cantu, Monica; Khoda Siddiki, Mahbube; Munoz-Rojas, David; Amade, Roger [Centre d' Investigacio en Nanociencia i Nanotecnologia (CIN2, CSIC), Laboratory of Nanostructured Materials for Photovoltaic Energy, Campus UAB, Barcelona (Spain); Gonzalez-Pech, Natalia I. [Centre d' Investigacio en Nanociencia i Nanotecnologia (CIN2, CSIC), Laboratory of Nanostructured Materials for Photovoltaic Energy, Campus UAB, Barcelona (Spain); Instituto Tecnologico y de Estudios Superiores de Monterrey (ITESM), Ave. Eugenio Garza Sada, 64640 Monterrey, N.L. (Mexico)

2010-07-15

Hybrid Solar Cells (HSC) applying Nb-TiO{sub 2} in direct contact with a conducting organic polymer, MEH-PPV, show higher stability than the bare TiO{sub 2}-based HSC when analyzed under inert atmosphere conditions. IPCE analyses revealed that inert atmospheres affect directly the semiconductor oxide in the first stages of the analyses but photovoltaic performance stabilizes after several hours. A 20 wt% Nb-doped TiO{sub 2} presented the highest stability and photovoltaic properties. The behavior has been attributed to the solubility limit of Nb within the TiO{sub 2} beyond 20 wt% doping level where the co-existence of NbO{sub 2} is observed. The HSCs were analyzed under controlled N{sub 2} atmosphere and 1000 W/m{sup 2} (AM 1.5) irradiation. (author)

Ionic Liquid Confined in Mesoporous Polymer Membrane with Improved Stability for CO2/N2 Separation

Directory of Open Access Journals (Sweden)

Ming Tan

2017-09-01

Full Text Available Supported ionic liquid membranes (SILMs have a promising prospect of application in flue gas separation, owing to its high permeability and selectivity of CO2. However, existing SILMs have the disadvantage of poor stability due to the loss of ionic liquid from the large pores of the macroporous support. In this study, a novel SILM with high stability was developed by confining ionic liquid in a mesoporous polymer membrane. First, a mesoporous polymer membrane derived from a soluble, low-molecular-weight phenolic resin precursor was deposited on a porous Al2O3 support, and then 1-ethyl-3-methylimidazolium tetrafluoroborate ([emim][BF4] was immobilized inside mesopores of phenolic resin, forming the SILM under vacuum. Effects of trans-membrane pressure difference on the SILM separation performance were investigated by measuring the permeances of CO2 and N2. The SILM exhibits a high ideal CO2/N2 selectivity of 40, and an actual selectivity of approximately 25 in a mixed gas (50% CO2 and 50% N2 at a trans-membrane pressure difference of 2.5 bar. Compared to [emim][BF4] supported by polyethersulfone membrane with a pore size of around 0.45 μm, the [emim][BF4] confined in a mesoporous polymer membrane exhibits an improved stability, and its separation performance remained stable for 40 h under a trans-membrane pressure difference of 1.5 bar in a mixed gas before the measurement was intentionally stopped.

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

Directory of Open Access Journals (Sweden)

J. C. McWilliams

2008-03-01

Full Text Available 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.

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

Energy Technology Data Exchange (ETDEWEB)

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

1993-12-01

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

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

International Nuclear Information System (INIS)

Lacan, A.

2009-04-01

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

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

Energy Technology Data Exchange (ETDEWEB)

Fairhall, A W

1973-09-07

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

Measurement of atmospheric CO2 column concentrations to cloud tops with a pulsed multi-wavelength airborne lidar

Science.gov (United States)

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.

Measurement of Atmospheric CO2 Column Concentrations to Cloud Tops With a Pulsed Multi-Wavelength Airborne Lidar

Science.gov (United States)

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;

CaO-Based CO2 Sorbents Effectively Stabilized by Metal Oxides.

Science.gov (United States)

Naeem, Muhammad Awais; Armutlulu, Andac; Imtiaz, Qasim; Müller, Christoph R

2017-11-17

Calcium looping (i.e., CO 2 capture by CaO) is a promising second-generation CO 2 capture technology. CaO, derived from naturally occurring limestone, offers an inexpensive solution, but due to the harsh operating conditions of the process, limestone-derived sorbents undergo a rapid capacity decay induced by the sintering of CaCO 3 . Here, we report a Pechini method to synthesize cyclically stable, CaO-based CO 2 sorbents with a high CO 2 uptake capacity. The sorbents synthesized feature compositional homogeneity in combination with a nanostructured and highly porous morphology. The presence of a single (Al 2 O 3 or Y 2 O 3 ) or bimetal oxide (Al 2 O 3 -Y 2 O 3 ) provides cyclic stability, except for MgO which undergoes a significant increase in its particle size with the cycle number. We also demonstrate a direct relationship between the CO 2 uptake and the morphology of the synthesized sorbents. After 30 cycles of calcination and carbonation, the best performing sorbent, containing an equimolar mixture of Al 2 O 3 and Y 2 O 3 , exhibits a CO 2 uptake capacity of 8.7 mmol CO 2  g -1 sorbent, which is approximately 360 % higher than that of the reference limestone. © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Using atmospheric CO2 data to assess a simplified carbon-climate simulation for the 20th century

International Nuclear Information System (INIS)

Law, Rachel M.; Kowalczyk, Eva A.; Wangs, Ying-Ping

2006-01-01

The CSIRO biosphere model has been coupled to an atmosphere model and a simulation has been performed for the 20th century. Both biosphere and atmosphere are forced with global CO 2 concentration and the atmosphere is also forced with prescribed sea surface temperatures. The simulation follows the C4MIP Phase 1 protocol. We assess the model simulation using atmospheric CO 2 data. Mauna Loa growth rate is well simulated from 1980 but overestimated before that time. The interannual variations in growth rate are reasonably reproduced. Seasonal cycles are underestimated in northern mid-latitudes and are out of phase in the southern hemisphere. The north-south gradient of annual mean CO 2 is substantially overestimated due to a northern hemisphere net biosphere source and a southern tropical sink. Diurnal cycles at three northern hemisphere locations are larger than observed in many months, most likely due to larger respiration than observed

Dispersive infrared spectroscopy measurements of atmospheric CO{sub 2} using a Fabry–Pérot interferometer sensor

Energy Technology Data Exchange (ETDEWEB)

Chan, K.L. [School of Energy and Environment, City University of Hong Kong (Hong Kong); Ning, Z., E-mail: zhining@cityu.edu.hk [School of Energy and Environment, City University of Hong Kong (Hong Kong); Guy Carpenter Climate Change Centre, City University of Hong Kong (Hong Kong); Westerdahl, D. [Ability R and D Energy Research Centre, City University of Hong Kong (Hong Kong); Wong, K.C. [School of Energy and Environment, City University of Hong Kong (Hong Kong); Sun, Y.W. [Anhui Institute of Optics and Fine Mechanics, Chinese Academy of Sciences, Hefei (China); Hartl, A. [School of Energy and Environment, City University of Hong Kong (Hong Kong); Wenig, M.O. [Meteorological Institute, Ludwig-Maximilians-Universität Munich (Germany)

2014-02-01

In this paper, we present the first dispersive infrared spectroscopic (DIRS) measurement of atmospheric carbon dioxide (CO{sub 2}) using a new scanning Fabry–Pérot interferometer (FPI) sensor. The sensor measures the optical spectra in the mid infrared (3900 nm to 5220 nm) wavelength range with full width half maximum (FWHM) spectral resolution of 78.8 nm at the CO{sub 2} absorption band (∼ 4280 nm) and sampling resolution of 20 nm. The CO{sub 2} concentration is determined from the measured optical absorption spectra by fitting it to the CO{sub 2} reference spectrum. Interference from other major absorbers in the same wavelength range, e.g., carbon monoxide (CO) and water vapor (H{sub 2}O), was taken out by including their reference spectra in the fit as well. The detailed descriptions of the instrumental setup, the retrieval procedure, a modeling study for error analysis as well as laboratory validation using standard gas concentrations are presented. An iterative algorithm to account for the non-linear response of the fit function to the absorption cross sections due to the broad instrument function was developed and tested. A modeling study of the retrieval algorithm showed that errors due to instrument noise can be considerably reduced by using the dispersive spectral information in the retrieval. The mean measurement error of the prototype DIRS CO{sub 2} measurement for 1 minute averaged data is about ± 2.5 ppmv, and down to ± 0.8 ppmv for 10 minute averaged data. A field test of atmospheric CO{sub 2} measurements were carried out in an urban site in Hong Kong for a month and compared to a commercial non-dispersive infrared (NDIR) CO{sub 2} analyzer. 10 minute averaged data shows good agreement between the DIRS and NDIR measurements with Pearson correlation coefficient (R) of 0.99. This new method offers an alternative approach of atmospheric CO{sub 2} measurement featuring high accuracy, correction of non-linear absorption and interference of water

Ultralow Parasitic Energy for Postcombustion CO ₂ Capture Realized in a Nickel Isonicotinate Metal–Organic Framework with Excellent Moisture Stability

Energy Technology Data Exchange (ETDEWEB)

Nandi, Shyamapada; Collins, Sean [Centre; amp, Department of Chemistry; Chakraborty, Debanjan; Banerjee, Debasis [Physical; Thallapally, Praveen K. [Physical; Woo, Tom K. [Centre; amp, Department of Chemistry; Vaidhyanathan, Ramanathan

2017-01-25

Metal-organic frameworks (MOFs) have attracted significant attention as solid sorbents in gas separation processes for low-energy postcombustion CO₂ capture. The parasitic energy (PE) has been put forward as a holistic parameter that measures how energy efficient (and therefore cost-effective) the CO₂ capture process will be using the material. In this work, we present a nickel isonicotinate based ultramicroporous MOF, 1 [Ni-(4PyC)(2)center dot DMF], that has the lowest PE for postcombustion CO, capture reported to date. We calculate a PE of 655 kJ/kg CO₂, which is lower than that of the best performing material previously reported, Mg-MOF-74. Further, 1 exhibits exceptional hydrolytic stability with the CO₂ adsorption isotherm being unchanged following 7 days of steam-treatment (>85% RH) or 6 months of exposure to the atmosphere. The diffusion coefficient of CO₂ in 1 is also 2 orders of magnitude higher than in zeolites currently used in industrial scrubbers. Breakthrough experiments show that 1 only loses 7% of its maximum CO₂ capacity under humid conditions.

Carbon isotopic evidence for the associations of decreasing atmospheric CO2 level with the Frasnian-Famennian mass extinction

Science.gov (United States)

Xu, Bing; Gu, Zhaoyan; Wang, Chengyuan; Hao, Qingzhen; Han, Jingtai; Liu, Qiang; Wang, Luo; Lu, Yanwu

2012-03-01

A perturbation of the global carbon cycle has often been used for interpreting the Frasnian-Famennian (F-F) mass extinction. However, the changes of atmospheric CO2 level (pCO2) during this interval are much debatable. To illustrate the carbon cycle during F-F transition, paired inorganic (δ13Ccarb) and organic (δ13Corg) carbon isotope analyses were carried out on two late Devonian carbonate sequences (Dongcun and Yangdi) from south China. The larger amplitude shift of δ13Corg compared to δ13Ccarb and its resultant Δ13C (Δ13C = δ13Ccarb - δ13Corg) decrease indicate decreased atmospheric CO2level around the F-F boundary. The onset ofpCO2 level decrease predates that of marine regressions, which coincide with the beginning of conodont extinctions, suggesting that temperature decrease induced by decreased greenhouse effect of atmospheric CO2might have contributed to the F-F mass extinction.

The Effect of Thermal Convection on Earth-Atmosphere CO2 Gas Exchange in Aggregated Soil

Science.gov (United States)

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.

Carbon Dioxide (CO2 Sequestration In Bio-Concrete, An Overview

Directory of Open Access Journals (Sweden)

Faisal Alshalif A.

2017-01-01

Full Text Available The emission of CO2 into atmosphere which has increased rapidly in the last years has led to global warming. Therefore, in order to overcome the negative impacts on human and environment, the researchers focused mainly on the reduction and stabilization of CO2 which represent the main contributor in the increasing global warming. The natural capturing and conversion of CO2 from atmosphere is taken place by biological, chemical and physical processes. However, these processes need long time to cause a significant reduction in CO2. Recently, scientists shifted to use green technologies that aimed to produce concrete with high potential to adsorb CO2 in order to accelerate the reduction of CO2. In the present review the potential of bio-concrete to sequestrate CO2 based on carbonation process and as a function of carbonic anhydrase (CA is highlighted. The factors affecting CO2 sequestration in concrete and bacterial species are discussed. It is evident from the literatures, that the new trends to use bio-concrete might contribute in the reduction of CO2 and enhance the strength of non-reinforced concrete.

Inter-annual changes in detritus-based food chains can enhance plant growth response to elevated atmospheric CO2.

Science.gov (United States)

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.

The annual averaged atmospheric dispersion factor and deposition factor according to methods of atmospheric stability classification

Energy Technology Data Exchange (ETDEWEB)

Jeong, Hae Sun; Jeong, Hyo Joon; Kim, Eun Han; Han, Moon Hee; Hwang, Won Tae [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of)

2016-09-15

This study analyzes the differences in the annual averaged atmospheric dispersion factor and ground deposition factor produced using two classification methods of atmospheric stability, which are based on a vertical temperature difference and the standard deviation of horizontal wind direction fluctuation. Daedeok and Wolsong nuclear sites were chosen for an assessment, and the meteorological data at 10 m were applied to the evaluation of atmospheric stability. The XOQDOQ software program was used to calculate atmospheric dispersion factors and ground deposition factors. The calculated distances were chosen at 400 m, 800 m, 1,200 m, 1,600 m, 2,400 m, and 3,200 m away from the radioactive material release points. All of the atmospheric dispersion factors generated using the atmospheric stability based on the vertical temperature difference were shown to be higher than those from the standard deviation of horizontal wind direction fluctuation. On the other hand, the ground deposition factors were shown to be same regardless of the classification method, as they were based on the graph obtained from empirical data presented in the Nuclear Regulatory Commission's Regulatory Guide 1.111, which is unrelated to the atmospheric stability for the ground level release. These results are based on the meteorological data collected over the course of one year at the specified sites; however, the classification method of atmospheric stability using the vertical temperature difference is expected to be more conservative.

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

NARCIS (Netherlands)

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

2011-01-01

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

The ignition delay, laminar flame speed and adiabatic temperature characteristics of n-pentane, n-hexane and n-heptane under O{sub 2}/CO{sub 2} atmosphere

Energy Technology Data Exchange (ETDEWEB)

Zhao, Ran [Huazhong Univ. of Science and Technology, Wuhan (China). State Key Lab. of Coal Combustion; Wuhan Textile Univ. (China). School of Environment and Urban Construction; Liu, Hao; Zhong, Xiaojiao; Wang, Zijian; Jin, Ziqin; Qiu, Jianrong [Huazhong Univ. of Science and Technology, Wuhan (China). State Key Lab. of Coal Combustion; Chen, Yingming [Wuhan Textile Univ. (China). School of Environment and Urban Construction

2013-07-01

Oxy-fuel (O{sub 2}/CO{sub 2}) combustion is one of the several promising new technologies which can realize the integrated control of CO{sub 2}, SO{sub 2}, NO{sub X} and other pollutants. However, when fuels are burned in the high CO{sub 2} concentration environment, the combustion characteristics can be very different from conventional air-fired combustion. Such changes imply that the high CO{sub 2} concentration atmosphere has impacts on the combustion processes. In this paper, the ignition time, laminar flame speed and adiabatic temperature property of C{sub 5} {proportional_to} C{sub 7} n-alkane fuels were studied under both ordinary air atmosphere and O{sub 2}/CO{sub 2} atmospheres over a wide range of CO{sub 2} concentration in the combustion systems. A new unified detailed chemical kinetic model was validated and used to simulate the three liquid hydrocarbon fuel's flame characteristics. Based on the verified model, the influences of various parameters (atmosphere, excess oxygen ratio, O{sub 2} concentration, CO{sub 2} concentration, and alkane type) on the C{sub 5} {proportional_to} C{sub 7} n-alkane's flame characteristics were systematically investigated. It can be concluded that high CO{sub 2} concentration atmosphere has negative effect on n-pentane, n-hexane and n-heptane flame's ignition, laminar flame speed and adiabatic temperature. Besides, this work confirms that high CO{sub 2} concentration atmosphere's chemical effects play a pronounced role on the flame characteristics, especially for the ignition time property.

Electronic structures and stability of Ni/Bi2Te3 and Co/Bi2Te3 interfaces

International Nuclear Information System (INIS)

Xiong Ka; Wang Weichao; Alshareef, Husam N; Gupta, Rahul P; Gnade, Bruce E; Cho, Kyeongjae; White, John B

2010-01-01

We investigate the electronic structures and stability for Ni/Bi 2 Te 3 , NiTe/Bi 2 Te 3 , Co/Bi 2 Te 3 and CoTe 2 /Bi 2 Te 3 interfaces by first-principles calculations. It is found that the surface termination strongly affects the band alignment. Ni and Co are found to form Ohmic contacts to Bi 2 Te 3 . The interface formation energy for Co/Bi 2 Te 3 interfaces is much lower than that of Ni/Bi 2 Te 3 interfaces. Furthermore, we found that NiTe on Bi 2 Te 3 is more stable than Ni, while the formation energies for Co and CoTe 2 on Bi 2 Te 3 are comparable.

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

Directory of Open Access Journals (Sweden)

Shuangxi Fang

2016-02-01

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

Elevated atmospheric CO2 negatively impacts photosynthesis through radiative forcing and physiology-mediated climate feedback

Science.gov (United States)

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.

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

Directory of Open Access Journals (Sweden)

J. Chappellaz

2011-05-01

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

Regional impacts of climate change and atmospheric CO2 on future ocean carbon uptake: A multi-model linear feedback analysis

OpenAIRE

Roy Tilla; Bopp Laurent; Gehlen Marion; Schneider Birgitt; Cadule Patricia; Frölicher Thomas; Segschneider Jochen; Tijputra Jerry; Heinze Christoph; Joos Fortunat

2011-01-01

The increase in atmospheric CO2 over this century depends on the evolution of the oceanic air–sea CO2 uptake which will be driven by the combined response to rising atmospheric CO2 itself and climate change. Here the future oceanic CO2 uptake is simulated using an ensemble of coupled climate–carbon cycle models. The models are driven by CO2 emissions from historical data and the Special Report on Emissions Scenarios (SRES) A2 high emission scenario. A linear feedback analysis successfully sep...

Trends in land surface phenology and atmospheric CO2 seasonality in the Northern Hemisphere terrestrial ecosystems

Science.gov (United States)

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.

Measurement of atmospheric CO2 column concentrations to cloud tops with a pulsed multi-wavelength airborne lidar

Directory of Open Access Journals (Sweden)

J. Mao

2018-01-01

Full Text Available 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.

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

Science.gov (United States)

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

2018-03-01

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

Carbon assimilation in Eucalyptus urophylla grown under high atmospheric CO2 concentrations: A proteomics perspective.

Science.gov (United States)

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

Carbon coated CoS_2 thermal battery electrode material with enhanced discharge performances and air stability

International Nuclear Information System (INIS)

Xie, Song; Deng, Yafeng; Mei, Jun; Yang, Zhaotang; Lau, Woon-Ming; Liu, Hao

2017-01-01

Graphical abstract: A novel carbon coated CoS_2 composite is prepared and investigated as a cathode material for thermal batteries. - Highlights: • A novel C@CoS_2 composite is successfully prepared by hydrothermal method. • The growth of CoS_2 in the glucose solution results in a smaller grain size. • The coating of carbon favors electron transfer and buffers polysulfides formation. • The in situ coated carbon layer effectively prevents the oxidation of CoS_2. • The C@CoS_2 composite shows competitive thermal stability and discharge property. - Abstract: Cobalt disulfide (CoS_2) is a promising thermal battery electrode material for its superior thermal stability and discharge performance. However, the low natural resource and poor air stability restrict its application in thermal battery fabrication. In this work, carbon coated CoS_2 composite was prepared by a facile one-pot hydrothermal method with glucose as carbon source. During the growth of CoS_2, the glucose molecules were in situ adsorbed and carbonized on the surface of the as-synthesized CoS_2, and the resultant carbon coating provided improved electrical conductivity and discharge performances to the composite. The thermal battery cell, which was fabricated with such a composite cathode and with a Li-Si anode, can output a capacity of 235.8 mAh g"−"1 and an energy density of 416.9 Wh kg"−"1 at a cut-off voltage of 1.7 V. This carbon coated CoS_2 composite also presented enhanced air stability. After being stored in dry air for 3 months, the composite can still provide a capacity of 232.4 mAh g"−"1 to 1.7 V, whereas the capacity of bare CoS_2 stored with the same condition dropped from 202.4 mAh g"−"1 to 189.7 mAh g"−"1.

Root Damage by Insects Reverses the Effects of Elevated Atmospheric CO2 on Eucalypt Seedlings

OpenAIRE

Johnson, Scott N.; Riegler, Markus

2013-01-01

Predicted increases in atmospheric carbon dioxide (CO2) are widely anticipated to increase biomass accumulation by accelerating rates of photosynthesis in many plant taxa. Little, however, is known about how soil-borne plant antagonists might modify the effects of elevated CO2 (eCO2), with root-feeding insects being particularly understudied. Root damage by insects often reduces rates of photosynthesis by disrupting root function and imposing water deficits. These insects therefore have consi...

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

Science.gov (United States)

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

2017-06-01

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