Agroforestry: a sustainable environmental practice for carbon sequestration under the climate change scenarios-a review.

PubMed

Abbas, Farhat; Hammad, Hafiz Mohkum; Fahad, Shah; Cerdà, Artemi; Rizwan, Muhammad; Farhad, Wajid; Ehsan, Sana; Bakhat, Hafiz Faiq

2017-04-01

Agroforestry is a sustainable land use system with a promising potential to sequester atmospheric carbon into soil. This system of land use distinguishes itself from the other systems, such as sole crop cultivation and afforestation on croplands only through its potential to sequester higher amounts of carbon (in the above- and belowground tree biomass) than the aforementioned two systems. According to Kyoto protocol, agroforestry is recognized as an afforestation activity that, in addition to sequestering carbon dioxide (CO 2 ) to soil, conserves biodiversity, protects cropland, works as a windbreak, and provides food and feed to human and livestock, pollen for honey bees, wood for fuel, and timber for shelters construction. Agroforestry is more attractive as a land use practice for the farming community worldwide instead of cropland and forestland management systems. This practice is a win-win situation for the farming community and for the environmental sustainability. This review presents agroforestry potential to counter the increasing concentration of atmospheric CO 2 by sequestering it in above- and belowground biomass. The role of agroforestry in climate change mitigation worldwide might be recognized to its full potential by overcoming various financial, technical, and institutional barriers. Carbon sequestration in soil by various agricultural systems can be simulated by various models but literature lacks reports on validated models to quantify the agroforestry potential for carbon sequestration.

Massive CO2 Ice Deposits Sequestered in the South Polar Layered Deposits of Mars

USGS Publications Warehouse

Phillips, Roger J.; Davis, Brian J.; Tanaka, Kenneth L.; Byrne, Shane; Mellon, Michael T.; Putzig, Nathaniel E.; Haberle, Robert M.; Kahre, Melinda A.; Campbell, Bruce A.; Carter, Lynn M.; Smith, Isaac B.; Holt, John W.; Smrekar, Suzanne E.; Nunes, Daniel C.; Plaut, Jeffrey J.; Egan, Anthony F.; Titus, Timothy N.; Seu, Roberto

2011-01-01

Shallow Radar soundings from the Mars Reconnaissance Orbiter reveal a buried deposit of carbon dioxide (CO2) ice within the south polar layered deposits of Mars with a volume of 9500 to 12,500 cubic kilometers, about 30 times that previously estimated for the south pole residual cap. The deposit occurs within a stratigraphic unit that is uniquely marked by collapse features and other evidence of interior CO2 volatile release. If released into the atmosphere at times of high obliquity, the CO2 reservoir would increase the atmospheric mass by up to 80%, leading to more frequent and intense dust storms and to more regions where liquid water could persist without boiling.

Making Mars habitable

NASA Technical Reports Server (NTRS)

Mckay, Christopher P.; Toon, Owen B.; Kasting, James F.

1991-01-01

The possibility is considered that the atmosphere and climate of Mars could be altered to allow terrestrial life forms, and possibly human beings, to survive on the surface. Production of CFCs or other greenhouse gases on Mars would warm the surface enough for the regolith and polar caps to release their CO2 and raise atmospheric pressure to 100 mbar. If a large regolith and polar CO2 reservoirs exist, the pressure would continue to rise on its own. If these are absent, additional CO2 would have to be released from carbonate minerals. At this point, perhaps between 100 and 100,000 yrs, Mars might be suitable for plants. If there is a mechanism for sequestering the reduced carbon, these plants could slowly transform the CO2 to produce an O2-rich atmosphere in perhaps 100,000 yrs. If sufficient N2 could be released from putative soil deposits and the CO2 level could be kept low enough, then a human-breathable atmosphere would be produced.

Long-term effects of elevated carbon dioxide concentration on sour orange wood specific gravity, modulus of elasticity, and microfibril angle

Treesearch

David Kretschmann; James Evans; Mike Wiemann; Bruce A. Kimball; Sherwood B. Idso

2007-01-01

The carbon dioxide (CO2) concentration of Earth’s atmosphere continues to rise. Plants in general are responsive to changing CO2 concentrations, which suggests changes in agricultural productivity in the United States and around the world. The ability of plants to absorb CO2 during photosynthesis and then store carbon in their structure or sequester it in the soil has...

Spatial and temporal variability in forest-atmosphere CO2 exchange

Treesearch

D.Y. Hollinger; J. Aber; B. Dail; E.A. Davidson; S.M. Goltz; et al.

2004-01-01

Seven years of carbon dioxide flux measurements indicate that a ∼ 90-year-old spruce dominated forest in Maine, USA, has been sequestering 174±46 gCm-2 yr-1 (mean±1 standard deviation, nocturnal friction velocity (u*) threshold >0.25ms-1...

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

NASA Technical Reports Server (NTRS)

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

1984-01-01

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

Mountain peatlands range from CO2 sinks at high elevations to sources at low elevations: Implications for a changing climate

Treesearch

David J. Millar; David J. Cooper; Kathleen A. Dwire; Robert M. Hubbard; Joseph von Fischer

2016-01-01

Mountain fens found in western North America have sequestered atmospheric carbon dioxide (CO2) for millennia, provide important habitat for wildlife, and serve as refugia for regionally-rare plant species typically found in boreal regions. It is unclear how Rocky Mountain fens are responding to a changing climate. It is possible that fens found at lower elevations may...

Upscaling nitrogen-mycorrhizal effects to quantify CO2 fertilization.

NASA Astrophysics Data System (ADS)

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

2016-12-01

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

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

PubMed

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

2016-02-11

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

Red mud as a carbon sink: variability, affecting factors and environmental significance.

PubMed

Si, Chunhua; Ma, Yingqun; Lin, Chuxia

2013-01-15

The capacity of red mud to sequester CO(2) varied markedly due to differences in bauxite type, processing and disposal methods. Calcium carbonates were the dominant mineral phases responsible for the carbon sequestration in the investigated red mud types. The carbon sequestration capacity of red mud was not fully exploited due to shortages of soluble divalent cations for formation of stable carbonate minerals. Titanate and silicate ions were the two major oxyanions that appeared to strongly compete with carbonate ions for the available soluble Ca. Supply of additional soluble Ca and Mg could be a viable pathway for maximizing carbon sequestration in red mud and simultaneously reducing the causticity of red mud. It is roughly estimated that over 100 million tonnes of CO(2) have been unintentionally sequestered in red mud around the world to date through the natural weathering of historically produced red mud. Based on the current production rate of red mud, it is likely that some 6 million tonnes of CO(2) will be sequestered annually through atmospheric carbonation. If appropriate technologies are in place for incorporating binding cations into red mud, approximately 6 million tonnes of additional CO(2) can be captured and stored in the red mud while the hazardousness of red mud is simultaneously reduced. Copyright © 2012 Elsevier B.V. All rights reserved.

An Analysis of the Climate Change Mitigation Potential through Soil Organic Carbon Sequestration in a Corn Belt Watershed.

PubMed

Bhattarai, Mukesh Dev; Secchi, Silvia; Schoof, Justin

2017-01-01

Land-based carbon sequestration constitutes a major low cost and immediately viable option in climate change mitigation. Using downscaled data from eight atmosphere-ocean general circulation models for a simulation period between 2015 and 2099, we examine the carbon sequestration potential of alternative agricultural land uses in an intensively farmed Corn Belt watershed and the impact of climate change on crop yields. Our results show that switching from conventional tillage continuous corn to no-till corn-soybean can sequester the equivalent of 192.1 MtCO 2 eq of soil organic carbon per hectare with a sequestration rate of 2.26 MtCO 2 eq ha -1 yr -1 . Our results also indicate that switchgrass can sequester the equivalent of 310.7 MtCO 2 eq of soil organic carbon per hectare with a sequestration rate of 3.65 MtCO 2 eq ha -1 yr -1 . Our findings suggest that, unlike for corn and soybean yields, climate change does not have a significant effect on switchgrass yields, possibly due to the carbon fertilization effect.

An Analysis of the Climate Change Mitigation Potential through Soil Organic Carbon Sequestration in a Corn Belt Watershed

NASA Astrophysics Data System (ADS)

Bhattarai, Mukesh Dev; Secchi, Silvia; Schoof, Justin

2017-01-01

Land-based carbon sequestration constitutes a major low cost and immediately viable option in climate change mitigation. Using downscaled data from eight atmosphere-ocean general circulation models for a simulation period between 2015 and 2099, we examine the carbon sequestration potential of alternative agricultural land uses in an intensively farmed Corn Belt watershed and the impact of climate change on crop yields. Our results show that switching from conventional tillage continuous corn to no-till corn-soybean can sequester the equivalent of 192.1 MtCO2 eq of soil organic carbon per hectare with a sequestration rate of 2.26 MtCO2 eq ha-1 yr-1. Our results also indicate that switchgrass can sequester the equivalent of 310.7 MtCO2 eq of soil organic carbon per hectare with a sequestration rate of 3.65 MtCO2 eq ha-1 yr-1. Our findings suggest that, unlike for corn and soybean yields, climate change does not have a significant effect on switchgrass yields, possibly due to the carbon fertilization effect.

A terrain-attribute based approach to assessing soil carbon sequestration in the Oregon Coast range mountains

EPA Science Inventory

Determining how to best mitigate Global Climate Change through the sequestration of atmospheric CO2 requires developing an understanding of potential ecosystem C sinks and the rates at which C can be sequestered in soils and vegetation under a variety of land uses. The largest g...

The effects of biochar and manure in silage corn

USDA-ARS?s Scientific Manuscript database

Amending soil with biochar may be a means of sequestering atmospheric CO2 and improving soil quality, but few multiyear field studies have examined the impacts of a one-time biochar application in an irrigated, calcareous soil. We fall-applied four treatments: dairy manure (18.7 tons/ac dry wt.); ha...

Biochar and manure effects on nitrogen nutrition in silage corn

USDA-ARS?s Scientific Manuscript database

Amending soil with biochar may be a means of sequestering atmospheric CO2 and improving soil quality, but few multiyear field studies have examined the impacts of a one-time biochar application in an irrigated, calcareous soil. Four treatments were applied in the fall 2008: dairy manure (18.7 tons/...

Carbon and nitrogen pools in oak-hickory forests of varying productivity

Treesearch

Donald J. Kaczmarek; Karyn S. Rodkey; Robert T. Reber; Phillip E. Pope; Felix, Jr. Ponder

1995-01-01

Carbon (C) and nitrogen (N) storage capacities are critical issues facing forest ecosystem management in the face of potential global climate change. The amount of C sequestered by forest ecosystems can be a significant sink for increasing atmospheric CO2 levels. N availability can interact with other environmental factors such as water...

Mountain respiration: Rates and patterns of fossil organic carbon oxidation revealed using the trace element rhenium

NASA Astrophysics Data System (ADS)

Hilton, R. G.; Gaillardet, J.; Calmels, D.; Birck, J.

2013-12-01

Fossil organic carbon (OCfossil) from sedimentary rocks can contribute to the carbon stock within the deepest part of soil. OCfossil constitutes a vast stock of carbon that was sequestered from the atmosphere in the geological past, containing ~15x106 PgC, which is approximately 25,000 times the carbon content of the pre-industrial atmosphere. Oxidation of OCfossil during chemical weathering at Earth's surface is thought to be a major source of carbon dioxide (CO2) to the atmosphere. It has been proposed that OCfossil oxidation occurs when fresh sedimentary rocks are exposed to oxygenated water, with the rate of CO2 release controlled by the supply of OCfossil to react. As such, mountain belts where high rates of physical erosion provide an abundant supply of OCfossil to the soil critical zone should be locations where this CO2 source is most potent. However, the rates of OCfossil oxidation during weathering remain poorly constrained. Here we use the trace element rhenium (Re) to shed new light on the rates and patterns of OCfossil oxidation across the landscape. Re is known to be associated with organic matter in rocks and following oxidation forms a soluble anion which contributes to the dissolved load of rivers. Rivers can offer an integrated signal of chemical reactions occurring across the landscape, and so by quantifying the dissolved Re flux we are able to estimate the corresponding release of CO2 by OCfossil weathering. Using a set of mountain river catchments in Taiwan, where water and sediment fluxes are well quantified, we estimate that the rates of CO2 output by this process are significant, and encroach on values expected for net biome productivity. We find that OCfossil oxidation rates are strongly linked to physical erosion rate at the catchment-scale. This suggests that changes in the rates of surface processes may alter this CO2 output from deep soils. On longer timescales, our findings suggest that the total CO2 output by OCfossil weathering in Taiwan does not negate estimates of CO2 sequestration by erosion and sedimentary burial of recent organic matter. Our findings suggest that mountain building in the tropic can result in a net sink of organic carbon during erosion and weathering which acts to sequester atmospheric CO2.

Evidence for carbon sequestration by agricultural liming

NASA Astrophysics Data System (ADS)

Hamilton, Stephen K.; Kurzman, Amanda L.; Arango, Clay; Jin, Lixin; Robertson, G. Philip

2007-06-01

Agricultural lime can be a source or a sink for CO2, depending on whether reaction occurs with strong acids or carbonic acid. Here we examine the impact of liming on global warming potential by comparing the sum of Ca2+ and Mg2+ to carbonate alkalinity in soil solutions beneath unmanaged vegetation versus limed row crops, and of streams and rivers in agricultural versus forested watersheds, mainly in southern Michigan. Soil solutions sampled by tension indicated that lime can act as either a source or a sink for CO2. However, infiltrating waters tended to indicate net CO2 uptake, as did tile drainage waters and streams draining agricultural watersheds. As nitrate concentrations increased in infiltrating waters, lime switched from a net CO2 sink to a source, implying nitrification as a major acidifying process. Dissolution of lime may sequester CO2 equal to roughly 25-50% of its C content, in contrast to the prevailing assumption that all of the carbon in lime becomes CO2. The ˜30 Tg/yr of agricultural lime applied in the United States could thus sequester up to 1.9 Tg C/yr, about 15% of the annual change in the U.S. CO2 emissions (12 Tg C/yr for 2002-2003). The implications of liming for atmospheric CO2 stabilization should be considered in strategies to mitigate global climate change.

Chemical, physical and biological factors affecting wood decomposition in forest soils

Treesearch

Martin Jurgensen; Peter Laks; David Reed; Anne Collins; Deborah Page-Dumroese; Douglas Crawford

2004-01-01

Organic matter (OM) decomposition is an important variable in forest productivity and determining the potential of forest soils to sequester atmospheric CO2 (Grigal and Vance 2000; Kimble et al. 2003). Studies using OM from a particular location gives site-specific decomposition information, but differences in OM type and quality make it difficult to compare results...

Forests, carbon and global climate.

PubMed

Malhi, Yadvinder; Meir, Patrick; Brown, Sandra

2002-08-15

This review places into context the role that forest ecosystems play in the global carbon cycle, and their potential interactions with climate change. We first examine the natural, preindustrial carbon cycle. Every year forest gross photosynthesis cycles approximately one-twelfth of the atmospheric stock of carbon dioxide, accounting for 50% of terrestrial photosynthesis. This cycling has remained almost constant since the end of the last ice age, but since the Industrial Revolution it has undergone substantial disruption as a result of the injection of 480 PgC into the atmosphere through fossil-fuel combustion and land-use change, including forest clearance. In the second part of this paper we review this 'carbon disruption', and its impact on the oceans, atmosphere and biosphere. Tropical deforestation is resulting in a release of 1.7 PgC yr(-1) into the atmosphere. However, there is also strong evidence for a 'sink' for carbon in natural vegetation (carbon absorption), which can be explained partly by the regrowth of forests on abandoned lands, and partly by a global change factor, the most likely cause being 'fertilization' resulting from the increase in atmospheric CO(2). In the 1990s this biosphere sink was estimated to be sequestering 3.2 PgC yr(-1) and is likely to have substantial effects on the dynamics, structure and biodiversity of all forests. Finally, we examine the potential for forest protection and afforestation to mitigate climate change. An extensive global carbon sequestration programme has the potential to make a particularly significant contribution to controlling the rise in CO2 emissions in the next few decades. In the course of the whole century, however, even the maximum amount of carbon that could be sequestered will be dwarfed by the magnitude of (projected) fossil-fuel emissions. Forest carbon sequestration should only be viewed as a component of a mitigation strategy, not as a substitute for the changes in energy supply, use and technology that will be required if atmospheric CO(2) concentrations are to be stabilized.

Assessing ocean alkalinity for carbon sequestration

NASA Astrophysics Data System (ADS)

Renforth, Phil; Henderson, Gideon

2017-09-01

Over the coming century humanity may need to find reservoirs to store several trillions of tons of carbon dioxide (CO2) emitted from fossil fuel combustion, which would otherwise cause dangerous climate change if it were left in the atmosphere. Carbon storage in the ocean as bicarbonate ions (by increasing ocean alkalinity) has received very little attention. Yet recent work suggests sufficient capacity to sequester copious quantities of CO2. It may be possible to sequester hundreds of billions to trillions of tons of C without surpassing postindustrial average carbonate saturation states in the surface ocean. When globally distributed, the impact of elevated alkalinity is potentially small and may help ameliorate the effects of ocean acidification. However, the local impact around addition sites may be more acute but is specific to the mineral and technology. The alkalinity of the ocean increases naturally because of rock weathering in which >1.5 mol of carbon are removed from the atmosphere for every mole of magnesium or calcium dissolved from silicate minerals (e.g., wollastonite, olivine, and anorthite) and 0.5 mol for carbonate minerals (e.g., calcite and dolomite). These processes are responsible for naturally sequestering 0.5 billion tons of CO2 per year. Alkalinity is reduced in the ocean through carbonate mineral precipitation, which is almost exclusively formed from biological activity. Most of the previous work on the biological response to changes in carbonate chemistry have focused on acidifying conditions. More research is required to understand carbonate precipitation at elevated alkalinity to constrain the longevity of carbon storage. A range of technologies have been proposed to increase ocean alkalinity (accelerated weathering of limestone, enhanced weathering, electrochemical promoted weathering, and ocean liming), the cost of which may be comparable to alternative carbon sequestration proposals (e.g., $20-100 tCO2-1). There are still many unanswered technical, environmental, social, and ethical questions, but the scale of the carbon sequestration challenge warrants research to address these.

Reimagining Carbon Sequestration in Fluviodeltaic Systems: Contributions from Clastic Overbank Deposits versus Peat

NASA Astrophysics Data System (ADS)

Jankowski, K. L.; Shen, Z.; Tornqvist, T. E.; Steponaitis, E.; Rosenheim, B. E.

2017-12-01

Understanding how natural systems sequester carbon, and at what rates, is critical for planning future climate change mitigation strategies. For the decade from 2006-2015, average annual CO2 emissions to the atmosphere ( 11 Pg C) are not completely offset by atmospheric retention and oceanic uptake ( 5 Pg C and 2.5 Pg C, respectively) (LeQuéré et al., 2016) implying residual terrestrial C sinks that are not fully understood. Rivers are increasingly recognized as playing a complex role in the global C cycle which, beyond acting as a source of CO2to the atmosphere, may act as a C sink. Here, we find that the mechanisms of C transfer through fluviodeltaic systems include various means of C storage and contribute significantly to the global unidentified terrestrial C sink. C sequestration by coastal wetlands - at a globally averaged rate of 200 g C/m2/yr - has been widely recognized as an important mechanism for terrestrial C sequestration, with less attention paid to the role of inland fluvial to deltaic deposition. We sampled three cores in the central Mississippi Delta for C content (using elemental analysis) and bulk density in fluviodeltaic overbank deposits as well as intercalated peat. We also established a flexible, Bayesian age-depth model using Bacon (Blaauw and Christen 2011) in order to calculate sediment accumulation rates from 14C and OSL ages. Peat deposits sequester C at an average rate of 40 g C/m2/yr. The relatively organic-poor overbank sediments sequester C at an average rate of 200 g C/m2/yr including what are likely punctuated periods of very fast deposition. While the episodic nature of overbank deposits make quantifying an annual impact difficult, it is clear that overbank deposition is an important and efficient mechanism for C sequestration in fluviodeltaic systems that deserves continued investigation.

Soil carbon stocks in Sarawak, Malaysia.

PubMed

Padmanabhan, E; Eswaran, H; Reich, P F

2013-11-01

The relationship between greenhouse gas emission and climate change has led to research to identify and manage the natural sources and sinks of the gases. CO2, CH4, and N2O have an anthropic source and of these CO2 is the least effective in trapping long wave radiation. Soil carbon sequestration can best be described as a process of removing carbon dioxide from the atmosphere and relocating into soils in a form that is not readily released back into the atmosphere. The purpose of this study is to estimate carbon stocks available under current conditions in Sarawak, Malaysia. SOC estimates are made for a standard depth of 100 cm unless the soil by definition is less than this depth, as in the case of lithic subgroups. Among the mineral soils, Inceptisols tend to generally have the highest carbon contents (about 25 kg m(-2) m(-1)), while Oxisols and Ultisols rate second (about 10-15 kg m(-2) m(-1)). The Oxisols store a good amount of carbon because of an appreciable time-frame to sequester carbon and possibly lower decomposition rates for the organic carbon that is found at 1m depths. Wet soils such as peatlands tend to store significant amounts of carbon. The highest values estimated for such soils are about 114 kg m(-2) m(-1). Such appreciable amounts can also be found in the Aquepts. In conclusion, it is pertinent to recognize that degradation of the carbon pool, just like desertification, is a real process and that this irreversible process must be addressed immediately. Therefore, appropriate soil management practices should be instituted to sequester large masses of soil carbon on an annual basis. This knowledge can be used effectively to formulate strategies to prevent forest fires and clearing: two processes that can quickly release sequestered carbon to the atmosphere in an almost irreversible manner. Copyright © 2013 Elsevier B.V. All rights reserved.

Preface

USGS Publications Warehouse

McPherson, Brian J.; Sundquist, Eric T.

2009-01-01

Carbon sequestration has emerged as an important option in policies to mitigate the increasing atmospheric concentrations of anthropogenic carbon dioxide (CO2). Significant quantities of anthropogenic CO2 are sequestered by natural carbon uptake in plants, soils, and the oceans. These uptake processes are objects of intense study by biogeochemists, ecologists, and other researchers who seek to understand the processes that determine the mass balance (“budget”) among global carbon fluxes. At the same time, many scientists and engineers are examining methods for deliberate carbon sequestration through storage in plants, soils, the oceans, and geological formations.

Impact erosion of the primordial atmosphere of Mars.

PubMed

Melosh, H J; Vickery, A M

1989-04-06

Abundant geomorphic evidence for fluvial processes on the surface of Mars suggests that during the era of heavy bombardment, Mars's atmospheric pressure was high enough for liquid water to flow on the surface. Many authors have proposed mechanisms by which Mars could have lost (or sequestered) an earlier, thicker atmosphere but none of these proposals has gained general acceptance. Here we examine the process of atmospheric erosion by impacts and show that it may account for an early episode of atmosphere loss from Mars. On the basis of this model, the primordial atmospheric pressure on Mars must have been in the vicinity of 1 bar, barring other sources or sinks of CO2. Current impact fluxes are too small to erode significantly the present martian atmosphere.

What does it take to detect a change in soil carbon stock? A regional comparison of minimum detectable difference and experiment duration in the North-Central United States

USDA-ARS?s Scientific Manuscript database

Accurate estimation of soil organic carbon (SOC) is crucial to efforts to improve soil fertility and stabilize atmospheric CO2 concentrations by sequestering carbon (C) in soils. Soil organic C measurements are, however, often highly variable and management practices can take a long time to produce ...

Achieving Negative CO2 Emissions by Protecting Ocean Chemistry

NASA Astrophysics Data System (ADS)

Cannara, A.

2016-12-01

Industrial Age CO2 added 1.8 trillion tons to the atmosphere. About ¼ has dissolved in seas. The rest still dissolves, bolstered by present emissions of >30 gigatons/year. Airborne & oceanic CO2 have induced sea warming & ocean acidification*. This paper suggests a way to induce a negative CO2-emissions environment for climate & oceans - preserve the planet`s dominant CO2-sequestration system ( 1 gigaton/year via calcifying sea life**) by promptly protecting ocean chemistry via expansion of clean power for both lime production & replacement of CO2-emitting sources. Provide natural alkali (CaO, MgO…) to oceans to maintain average pH above 8.0, as indicated by marine biologists. That alkali (lime) is available from past calcifying life's limestone deposits, so can be returned safely to seas once its CO2 is removed & permanently sequestered (Carbfix, BSCP, etc.***). Limestone is a dense source of CO2 - efficient processing per mole sequestered. Distribution of enough lime is possible via cargo-ship transits - 10,000 tons lime/transit, 1 million transits/year. New Panamax ships carry 120,000 tons. Just 10,000/transit allows gradual reduction of present & past CO2 emissions effects, if coupled with combustion-power reductions. CO2 separation from limestone, as in cement plants, consumes 400kWHrs of thermal energy per ton of output lime (or CO2). To combat yearly CO2 dissolution in seas, we must produce & distribute about 10gigatons of lime/year. Only nuclear power produces the clean energy (thousands of terawatt hours) to meet this need - 1000 dedicated 1GWe reactors, processing 12 cubic miles of limestone/year & sequestering CO2 into a similar mass of basalt. Basalt is common in the world. Researchers*** report it provides good, mineralized CO2 sequestration. The numbers above allow gradual CO2 reduction in air and seas, if we return to President Kennedy's energy path: http://tinyurl.com/6xgpkfa We're on an environmental precipice due to failure to eliminate combustion power by 2000, per JFK. Brewer says oceans are in "precarious balance". Robust action now gradually restores a safer environment through ocean protection. * "A short history of ocean acidification science in the 20th century", Brewer, MBARI, 2013. ** AAAS Science, Canfield & Kump, 1 Feb. 2013. *** AAAS Science, Mattcr et alia, 10 Jun 2016.

Ecological Limits to Terrestrial Carbon Dioxide Removal Strategies

NASA Astrophysics Data System (ADS)

Smith, L. J.; Torn, M. S.; Jones, A. D.

2011-12-01

Carbon dioxide removal from the atmosphere through terrestrial carbon sequestration and bioenergy (biological CDR) is a proposed climate change mitigation strategy. Biological CDR increases the carbon storage capacity of soils and biomass through changes in land cover and use, including reforestation, afforestation, conversion of land to agriculture for biofuels, conversion of degraded land to grassland, and alternative management practices such as conservation tillage. While biological CDR may play a valuable role in future climate change mitigation, many of its proponents fail to account for the full range of biological, biophysical, hydrologic, and economic complexities associated with proposed land use changes. In this analysis, we identify and discuss a set of ecological limits and impacts associated with terrestrial CDR. The capacity of biofuels, soils, and other living biomass to sequester carbon may be constrained by nutrient and water availability, soil dynamics, and local climate effects, all of which can change spatially and temporally in unpredictable ways. Even if CDR is effective at sequestering CO2, its associated land use and land cover changes may negatively impact ecological resources by compromising water quality and availability, degrading soils, reducing biodiversity, displacing agriculture, and altering local climate through albedo and evapotranspiration changes. Measures taken to overcome ecological limitations, such as fertilizer addition and irrigation, may exacerbate these impacts even further. The ecological considerations and quantitative analyses that we present highlight uncertainties introduced by ecological complexity, disagreements between models, perverse economic incentives, and changing environmental factors. We do not reject CDR as a potentially valuable strategy for climate change mitigation; ecosystem protection, restoration, and improved management practices could enhance soil fertility and protect biodiversity while reducing increases in atmospheric CO2. Rather, we emphasize the importance of evaluating the full set of biological, physical, economic, and political realities that accompany land-use changes and manipulations to the carbon cycle. While the immediate goal of biological CDR is to reduce atmospheric CO2 concentrations, its ultimate goal in mitigating climate change is to reduce the threats to ecosystems and society. Sequestering carbon at the cost of ecosystem health would not be a sensible approach.

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

NASA Astrophysics Data System (ADS)

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

2017-12-01

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

Outgassing of the Eastern Equatorial Pacific during the Pliocene period.

NASA Astrophysics Data System (ADS)

Guillermic, M.; Tripati, A.

2016-12-01

The transition from the warm, ice-free conditions of the early Cenozoic to present-day glacial state with ice sheets in both hemispheres has been ascribed to long- and short-term changes in atmospheric CO2. The processes causing long-term changes in atmospheric CO2 levels are of debate. One possible explanation for changes in atmospheric CO2 relates to changes in air-sea exchange due to fluctuations in ocean carbon sources and sinks, as modulated by the stratification of surface waters. While nutrient consumption in low-latitude environments and associated export of CO2 to the deep sea works to sequester CO2 in the ocean interior, the return of deep water to the surface in the high latitudes and upwelling at the equator and in the eastern portion of ocean basins releases CO2. Quantitative estimates for surface water pH and pCO2 in different regions of the ocean and identification of CO2-sources and sinks are needed to better understand the role of the ocean in driving and/or amplifying variations in the atmospheric CO2 reservoir and climate change. Here we present preliminary results of surface water pH for the early Pliocene to Holocene based on boron isotope measurements of planktic foraminifera for the Eastern Equatorial Pacific. We develop records of B/Ca, Mg/Ca ratios, boron isotopes, and oxygen isotopes measurements in foraminifera tests (Globigeneroides sacculifer, Globigeneroides ruber, Neogloboquadrina dutertrei). We reconstruct changes in ocean CO2 outgassing in the Eastern Equatorial Pacific using records from ODP Site 847 (0°N, 95°W, 3373 m water depth). These data are used to examine if there is evidence for changes in stratification and CO2 outgassing during the early Pliocene warm period and during Pliocene intensification of Northern Hemisphere glaciation.

Apparatus for extracting and sequestering carbon dioxide

DOEpatents

Rau, Gregory H [Castro Valley, CA; Caldeira, Kenneth G [Livermore, CA

2010-02-02

An apparatus and method associated therewith to extract and sequester carbon dioxide (CO.sub.2) from a stream or volume of gas wherein said apparatus hydrates CO.sub.2 and reacts the resulting carbonic acid with carbonate. Suitable carbonates include, but are not limited to, carbonates of alkali metals and alkaline earth metals, preferably carbonates of calcium and magnesium. Waste products are metal cations and bicarbonate in solution or dehydrated metal salts, which when disposed of in a large body of water provide an effective way of sequestering CO.sub.2 from a gaseous environment.

Method for extracting and sequestering carbon dioxide

DOEpatents

Rau, Gregory H.; Caldeira, Kenneth G.

2005-05-10

A method and apparatus to extract and sequester carbon dioxide (CO.sub.2) from a stream or volume of gas wherein said method and apparatus hydrates CO.sub.2, and reacts the resulting carbonic acid with carbonate. Suitable carbonates include, but are not limited to, carbonates of alkali metals and alkaline earth metals, preferably carbonates of calcium and magnesium. Waste products are metal cations and bicarbonate in solution or dehydrated metal salts, which when disposed of in a large body of water provide an effective way of sequestering CO.sub.2 from a gaseous environment.

The role of nutricline depth in regulating the ocean carbon cycle.

PubMed

Cermeño, Pedro; Dutkiewicz, Stephanie; Harris, Roger P; Follows, Mick; Schofield, Oscar; Falkowski, Paul G

2008-12-23

Carbon uptake by marine phytoplankton, and its export as organic matter to the ocean interior (i.e., the "biological pump"), lowers the partial pressure of carbon dioxide (pCO(2)) in the upper ocean and facilitates the diffusive drawdown of atmospheric CO(2). Conversely, precipitation of calcium carbonate by marine planktonic calcifiers such as coccolithophorids increases pCO(2) and promotes its outgassing (i.e., the "alkalinity pump"). Over the past approximately 100 million years, these two carbon fluxes have been modulated by the relative abundance of diatoms and coccolithophores, resulting in biological feedback on atmospheric CO(2) and Earth's climate; yet, the processes determining the relative distribution of these two phytoplankton taxa remain poorly understood. We analyzed phytoplankton community composition in the Atlantic Ocean and show that the distribution of diatoms and coccolithophorids is correlated with the nutricline depth, a proxy of nutrient supply to the upper mixed layer of the ocean. Using this analysis in conjunction with a coupled atmosphere-ocean intermediate complexity model, we predict a dramatic reduction in the nutrient supply to the euphotic layer in the coming century as a result of increased thermal stratification. Our findings indicate that, by altering phytoplankton community composition, this causal relationship may lead to a decreased efficiency of the biological pump in sequestering atmospheric CO(2), implying a positive feedback in the climate system. These results provide a mechanistic basis for understanding the connection between upper ocean dynamics, the calcium carbonate-to-organic C production ratio and atmospheric pCO(2) variations on time scales ranging from seasonal cycles to geological transitions.

Sequestering ADM ethanol plant carbon dioxide

USGS Publications Warehouse

Finley, R.J.; Riddle, D.

2008-01-01

Archer Daniels Midland Co. (ADM) and the Illinois State Geological Survey (ISGS) are collaborating on a project in confirming that a rock formation can store carbon dioxide from the plant in its pores. The project aimed to sequester the gas underground permanently to minimize release of the greenhouse gas into the atmosphere. It is also designed to store one million tons of carbon dioxide over a three-year period. The project is worth $84.3M, funded by $66.7M from the US Department Energy, supplemented by co-funding from ADM and other corporate and state resources. The project will start drilling of wells to an expected depth over 6500 feet into the Mount Simon Sandstone formation.

Undoing climate warming by atmospheric carbon-dioxide removal: can a holocene-like climate be restored?

NASA Astrophysics Data System (ADS)

MacDougall, Andrew

2013-04-01

Understandably, most climate modelling studies of future climate have focused on the affects of carbon emissions in the present century or the long-term fate of anthropogenically emitted carbon. These studies make an assumption: that once net anthropogenic carbon emissions cease, that humanity will make no further effort to intervene in atmospheric composition. There is a case to be made, however, that there will be a desire to return to a "safe" atmospheric concentration of CO2. Realistically this implies synthetically removing CO2 from the atmosphere and storing it is some geologically stable form. For this study experiments were conducted using the University of Victoria Earth System Climate Model (UVic ESCM) forced with novel future atmospheric trace-gas concentration pathways to explore a gradual return to pre-industrial radiative forcing. The concentration pathways follow each RCP (2.6, 4.5, 6.0, and 8.5) exactly until the peak CO2 concentration of that RCP is reached, at which point atmospheric CO2 is reduced at the same rate it increased until the 1850 concentration of CO2 is reached. Non-CO2 greenhouse gas forcing follows the prescribed RCP path until the year of peak CO2, then is subsequently linearly reduced to pre-industrial forcing. Pasture and crop areas are also gradually reduced to their pre-industrial extent. Under the middle two concentration pathways (4.5 and 6.0) a climate resembling the 20th century climate can be restored by the 25th century, although surface temperature remains above the pre-industrial temperature until at least the 30th century. Due to carbon-cycle feedbacks the quantity of carbon that must be removed from the atmosphere is larger than the quantity that was originally emitted. For concentration pathways 2.6, 4.5, and 6.0 the sequestered CO2 is 115-190% of the original cumulative carbon emissions. These results suggest that even with monumental effort to remove CO2 from the atmosphere, humanity will be living with the consequences of fossil fuel emissions for a very long time.

The radiogenic and stable Sr isotope geochemistry of basalt weathering in Iceland: Role of hydrothermal calcite and implications for long-term climate regulation

NASA Astrophysics Data System (ADS)

Andrews, M. Grace; Jacobson, Andrew D.

2017-10-01

Several studies have examined the geochemistry of Icelandic rivers to quantify the relationship between basalt weathering and long-term climate regulation. Recent research has suggested that the chemical weathering of hydrothermal and metamorphic calcite contributes significant quantities of HCO3- to the Icelandic riverine flux (Jacobson et al., 2015). Because the HCO3- derives from volcanic CO2 that was sequestered in mineral form prior to atmospheric injection, the strength of the basalt weathering feedback occurring in Iceland may be lower than previously realized. To test these hypotheses, we analyzed the radiogenic and stable Sr isotope composition (87Sr/86Sr and δ88/86Sr) of the same suite of water, rock, and mineral samples as examined in Jacobson et al. (2015), and we developed a simple model of the long-term C cycle that considers the transformation of volcanic CO2 to HCO3- during subsurface silicate weathering, which is a precursor to hydrothermal calcite formation. Interpretations based on 87Sr/86Sr and Ca/Sr ratios suggest that conservative, three-component mixing between basalt, calcite, and atmospheric deposition adequately explains river geochemistry. On average, the δ88/86Sr values of glacial and non-glacial rivers (0.414‰ and 0.388‰, respectively) are generally higher than those for basalt (0.276‰); however, calcite δ88/86Sr values (0.347‰) are also higher than those for basalt and span the range of riverine values. Thus, riverine δ88/86Sr values are also consistent three-component mixing between basalt, calcite, and atmospheric deposition. Isotopic fractionation is not required to explain riverine trends. Finally, model equations for the long-term C cycle demonstrate that subsurface silicate weathering reduces the magnitude of the volcanic CO2 degassing flux, which in turn causes the atmosphere to stabilize at lower pCO2 values compared to the case where no subsurface silicate weathering occurs. However, the proportion of the net volcanic C flux introduced to the atmosphere-ocean system as HCO3- after subsurface silicate weathering does not regulate long-term climate. Because hydrothermal calcite simply sequesters some of this HCO3- and delays its transmission to the atmosphere-ocean system until it dissolves at the surface later in time, it can be concluded the weathering of hydrothermal calcite bearing non-atmospheric C also has no effect on long-term climate regulation. Icelandic riverine HCO3- fluxes should be corrected for the hydrothermal calcite weathering contribution prior to quantifying atmospheric CO2 consumption rates by basalt weathering at the Earth's surface.

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

PubMed Central

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

2014-01-01

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

An Evaluation of the Feasibility of Combining Carbon Dioxide Flooding Technologies with Microbial Enhanced Oil Recovery Technologies in Order To Sequester Carbon Dioxide

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

Todd French; Lew Brown; Rafael Hernandez

2009-08-19

The need for more energy as our population grows results in an increase in the amount of CO2 introduced into the atmosphere. The effect of this introduction is currently debated intensely as to the severity of the effect of this. The bjective of this investigation was to determine if the production of more energy (i.e. petroleum) and the sequestration of CO2 could be coupled into one process. Carbon dioxide flooding is a well-established technique that introduces Compressed CO2 into a subsurface oil-bearing formation to aide in liquefying harder to extract petroleum and enhancing its mobility towards the production wells.

Stem biomass, C and N partitioning and growth efficiency of mature pedigreed black spruce on both a wet and a dry site.

Treesearch

John Major; Kurt Johnsen; Debra Barsi; Moira Campbell; John Malcolm

2013-01-01

Worldwide, efforts to manage atmospheric CO2 are being explored both by reducing emissions and by sequestering more carbon (C). Stem biomass, C, and nitrogen (N) parameters were measured in plots of first-generation (F1), 32-year-old black spruce (Picea mariana (Mill.) B.S.P.) from four full-sib families studied previously for drought tolerance and differential...

EERC Center for Biomass Utilization 2008-2010. Phases I-III

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

Zygarlicke, Christopher J.; Hurley, John P.; Auich, Ted R.

The U.S. Department of Energy (DOE) Energy Information Administration (EIA) projects nonhydro renewable electric energy increases of 140% and liquid transportation biofuels growing by 32,200 barrels a day between 2012 and 2040 (U.S. Energy Information Administration, 2014). This is the EIA base case scenario, and this outlook could be a low estimate depending on the many assumptions involved in making such projections, not the least of which are climate change and the resultant legislation. The climate change postulate is based on increasing levels of CO 2 being introduced into the atmosphere through anthropogenic activity such as fossil fuel combustion formore » energy use. Renewable energy, and biomass conversion to energy in particular, is a net-zero CO 2 emission generator. When biomass is converted to energy, it emits CO 2; however, this CO 2 is balanced in a cycle where the production of biomass removes CO 2 from the atmosphere for growth and then releases it back into the atmosphere to be taken up by new growth of biomass feedstocks for energy. In comparison, fossil fuels are examples of CO 2 that has been removed from the atmosphere and sequestered and which, when converted to energy, is a new addition to the atmospheric levels of CO 2, which has been linked to climate change. While recent advances in technology used for extracting oil and gas from tight formations have increased the availability of fossil fuels for energy, the end game needs to focus on providing sustainable energy sources for the United States as well as the world. If, in the future, legislation is enacted that places a fee on atmospheric CO 2 emissions, this may make the use of biomass for energy more economically attractive, increasing its use. Research that focuses on the future sustainability of energy production is part of the answer to bringing about game-changing technologies that can provide energy in a timely, reliable, sustainable fashion.« less

Plant Regrowth as a Driver of Recent Enhancement of Terrestrial CO2 Uptake

NASA Astrophysics Data System (ADS)

Kondo, Masayuki; Ichii, Kazuhito; Patra, Prabir K.; Poulter, Benjamin; Calle, Leonardo; Koven, Charles; Pugh, Thomas A. M.; Kato, Etsushi; Harper, Anna; Zaehle, Sönke; Wiltshire, Andy

2018-05-01

The increasing strength of land CO2 uptake in the 2000s has been attributed to a stimulating effect of rising atmospheric CO2 on photosynthesis (CO2 fertilization). Using terrestrial biosphere models, we show that enhanced CO2 uptake is induced not only by CO2 fertilization but also an increasing uptake by plant regrowth (accounting for 0.33 ± 0.10 Pg C/year increase of CO2 uptake in the 2000s compared with the 1960s-1990s) with its effect most pronounced in eastern North America, southern-eastern Europe, and southeastern temperate Eurasia. Our analysis indicates that ecosystems in North America and Europe have established the current productive state through regrowth since the 1960s, and those in temperate Eurasia are still in a stage from regrowth following active afforestation in the 1980s-1990s. As the strength of model representation of CO2 fertilization is still in debate, plant regrowth might have a greater potential to sequester carbon than indicated by this study.

Tolerance of allogromiid Foraminifera to severely elevated carbon dioxide concentrations: Implications to future ecosystem functioning and paleoceanographic interpretations

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

Bernhard, Joan M.; Mollo-Christensen, Elizabeth; Eisenkolb, Nadine

2009-02-01

Increases in the partial pressure of carbon dioxide (pCO2) in the atmosphere will significantly affect a wide variety of terrestrial fauna and flora. Because of tight atmospheric oceanic coupling, shallow-water marine species are also expected to be affected by increases in atmospheric carbon dioxide concentrations. One proposed way to slow increases in atmospheric pCO2 is to sequester CO2 in the deep sea. Thus, over the next few centuries marine species will be exposed to changing seawater chemistry caused by ocean atmospheric exchange and/or deep-ocean sequestration. This initial case study on one allogromiid foraminiferal species (Allogromia laticollaris) was conducted to beginmore » to ascertain the effect of elevated pCO2 on benthic Foraminifera, which are a major meiofaunal constituent of shallow- and deep-water marine communities. Cultures of this thecate foraminiferan protist were used for 10-14-day experiments. Experimental treatments were executed in an incubator that controlled CO2 (15000; 30 000; 60 000; 90 000; 200 000 ppm), temperature and humidity; atmospheric controls (i.e., ~375 ppm CO2) were executed simultaneously. Although the experimental elevated pCO2 values are far above foreseeable surface water pCO2, they were selected to represent the spectrum of conditions expected for the benthos if deep-sea CO2 sequestration becomes a reality. Survival was assessed in two independent ways: pseudopodial presence/absence and measurement of adenosine triphosphate (ATP), which is an indicator of cellular energy. Substantial proportions of A. laticollaris populations survived 200 000 ppm CO2 although the mean of the median [ATP] of survivors was statistically lower for this treatment than for that of atmospheric control specimens. After individuals that had been incubated in 200 000 ppm CO2 for 12 days were transferred to atmospheric conditions for ~24 h, the [ATP] of live specimens (survivors) approximated those of the comparable atmospheric control treatment. Incubation in 200 000 ppm CO2 also resulted in reproduction by some individuals. Results suggest that certain Foraminifera are able to tolerate deep-sea CO2 sequestration and perhaps thrive as a result of elevated pCO2 that is predicted for the next few centuries, in a high-pCO2 world. Thus, allogromiid foraminiferal blooms may result from climate change. Furthermore, because allogromiids consume a variety of prey, it is likely that they will be major players in ecosystem dynamics of future coastal sedimentary environments.« less

Tolerance of allogromiid Foraminifera to severely elevated carbon dioxide concentrations: Implications to future ecosystem functioning and paleoceanographic interpretations

NASA Astrophysics Data System (ADS)

Bernhard, Joan M.; Mollo-Christensen, Elizabeth; Eisenkolb, Nadine; Starczak, Victoria R.

2009-02-01

Increases in the partial pressure of carbon dioxide (pCO 2) in the atmosphere will significantly affect a wide variety of terrestrial fauna and flora. Because of tight atmospheric-oceanic coupling, shallow-water marine species are also expected to be affected by increases in atmospheric carbon dioxide concentrations. One proposed way to slow increases in atmospheric pCO 2 is to sequester CO 2 in the deep sea. Thus, over the next few centuries marine species will be exposed to changing seawater chemistry caused by ocean-atmospheric exchange and/or deep-ocean sequestration. This initial case study on one allogromiid foraminiferal species ( Allogromia laticollaris) was conducted to begin to ascertain the effect of elevated pCO 2 on benthic Foraminifera, which are a major meiofaunal constituent of shallow- and deep-water marine communities. Cultures of this thecate foraminiferan protist were used for 10-14-day experiments. Experimental treatments were executed in an incubator that controlled CO 2 (15 000; 30 000; 60 000; 90 000; 200 000 ppm), temperature and humidity; atmospheric controls (i.e., ~ 375 ppm CO 2) were executed simultaneously. Although the experimental elevated pCO 2 values are far above foreseeable surface water pCO 2, they were selected to represent the spectrum of conditions expected for the benthos if deep-sea CO 2 sequestration becomes a reality. Survival was assessed in two independent ways: pseudopodial presence/absence and measurement of adenosine triphosphate (ATP), which is an indicator of cellular energy. Substantial proportions of A. laticollaris populations survived 200 000 ppm CO 2 although the mean of the median [ATP] of survivors was statistically lower for this treatment than for that of atmospheric control specimens. After individuals that had been incubated in 200 000 ppm CO 2 for 12 days were transferred to atmospheric conditions for ~ 24 h, the [ATP] of live specimens (survivors) approximated those of the comparable atmospheric control treatment. Incubation in 200 000 ppm CO 2 also resulted in reproduction by some individuals. Results suggest that certain Foraminifera are able to tolerate deep-sea CO 2 sequestration and perhaps thrive as a result of elevated pCO 2 that is predicted for the next few centuries, in a high-pCO 2 world. Thus, allogromiid foraminiferal "blooms" may result from climate change. Furthermore, because allogromiids consume a variety of prey, it is likely that they will be major players in ecosystem dynamics of future coastal sedimentary environments.

Rising CO2 Levels Will Intensify Phytoplankton Blooms in Eutrophic and Hypertrophic Lakes

PubMed Central

Verspagen, Jolanda M. H.; Van de Waal, Dedmer B.; Finke, Jan F.; Visser, Petra M.; Van Donk, Ellen; Huisman, Jef

2014-01-01

Harmful algal blooms threaten the water quality of many eutrophic and hypertrophic lakes and cause severe ecological and economic damage worldwide. Dense blooms often deplete the dissolved CO2 concentration and raise pH. Yet, quantitative prediction of the feedbacks between phytoplankton growth, CO2 drawdown and the inorganic carbon chemistry of aquatic ecosystems has received surprisingly little attention. Here, we develop a mathematical model to predict dynamic changes in dissolved inorganic carbon (DIC), pH and alkalinity during phytoplankton bloom development. We tested the model in chemostat experiments with the freshwater cyanobacterium Microcystis aeruginosa at different CO2 levels. The experiments showed that dense blooms sequestered large amounts of atmospheric CO2, not only by their own biomass production but also by inducing a high pH and alkalinity that enhanced the capacity for DIC storage in the system. We used the model to explore how phytoplankton blooms of eutrophic waters will respond to rising CO2 levels. The model predicts that (1) dense phytoplankton blooms in low- and moderately alkaline waters can deplete the dissolved CO2 concentration to limiting levels and raise the pH over a relatively wide range of atmospheric CO2 conditions, (2) rising atmospheric CO2 levels will enhance phytoplankton blooms in low- and moderately alkaline waters with high nutrient loads, and (3) above some threshold, rising atmospheric CO2 will alleviate phytoplankton blooms from carbon limitation, resulting in less intense CO2 depletion and a lesser increase in pH. Sensitivity analysis indicated that the model predictions were qualitatively robust. Quantitatively, the predictions were sensitive to variation in lake depth, DIC input and CO2 gas transfer across the air-water interface, but relatively robust to variation in the carbon uptake mechanisms of phytoplankton. In total, these findings warn that rising CO2 levels may result in a marked intensification of phytoplankton blooms in eutrophic and hypertrophic waters. PMID:25119996

Current land cover in the tropics and its potential for sequestering carbon

NASA Astrophysics Data System (ADS)

Houghton, R. A.; Unruh, J. D.; Lefebvre, P. A.

1993-06-01

Emissions of carbon dioxide and other greenhouse gases from human activity are increasing the concentrations of these gases in the atmosphere. The Earth is expected to warm as a result, with consequences that are potentially highly disruptive to human societies. Reductions in the use of fossil fuels and in rates of deforestation worldwide will reduce emissions of CO2, but atmospheric concentrations will continue to increase unless emissions are reduced by more than 60% (about 4.5 billion tons of carbon annually). Reforestation seems to offer one of the few means for reducing the atmospheric concentration of CO2 over periods as short as human generations. We report here an approach for evaluating the potential for reforestation to help stabilize or even reduce the concentration of CO2 in the atmosphere. Reforestation is defined broadly to include tree plantations, natural regrowth of secondary forests, and the practice of agroforestry. Our premise is that human use of the land has generally reduced woody biomass and that such lands have a potential for reaccumulating carbon if appropriately managed. We used published ground studies together with global vegetation index data from the NOAA 7 satellite to estimate current land cover in tropical regions. Then, superimposing this map of current land cover over maps depicting the distribution of vegetation cover prior to human disturbance, we obtained an estimate of about 3200 X 106 ha in the tropics (almost 60% of the total land area considered) where woody biomass had been decreased, and where carbon might again be sequestered. We calculated the amount of carbon that could be withdrawn from the atmosphere and stored in woody biomass if several management options were implemented. Biomass accumulations were determined from forestry statistics. Application of the data on biomass to the areas suitable for accumulation of carbon yielded an estimate of potential accumulation of 160-170 Pg carbon, an amount equivalent to the accumulation of carbon in the atmosphere since the start of the industrial revolution, or to about 25 years of fossil fuel emissions at current rates. Estimates of both area and potential accumulation of carbon were crude, probably not better than ±50%. They are useful for suggesting the role that tropical lands might play in stabilizing atmospheric concentrations of CO2, but they should not be used to suggest specific management options in individual countries. As maps with higher spatial resolution become available, however, the method should provide more precise estimates overall and in specific locations.

The role of nutricline depth in regulating the ocean carbon cycle

PubMed Central

Cermeño, Pedro; Dutkiewicz, Stephanie; Harris, Roger P.; Follows, Mick; Schofield, Oscar; Falkowski, Paul G.

2008-01-01

Carbon uptake by marine phytoplankton, and its export as organic matter to the ocean interior (i.e., the “biological pump”), lowers the partial pressure of carbon dioxide (pCO2) in the upper ocean and facilitates the diffusive drawdown of atmospheric CO2. Conversely, precipitation of calcium carbonate by marine planktonic calcifiers such as coccolithophorids increases pCO2 and promotes its outgassing (i.e., the “alkalinity pump”). Over the past ≈100 million years, these two carbon fluxes have been modulated by the relative abundance of diatoms and coccolithophores, resulting in biological feedback on atmospheric CO2 and Earth's climate; yet, the processes determining the relative distribution of these two phytoplankton taxa remain poorly understood. We analyzed phytoplankton community composition in the Atlantic Ocean and show that the distribution of diatoms and coccolithophorids is correlated with the nutricline depth, a proxy of nutrient supply to the upper mixed layer of the ocean. Using this analysis in conjunction with a coupled atmosphere–ocean intermediate complexity model, we predict a dramatic reduction in the nutrient supply to the euphotic layer in the coming century as a result of increased thermal stratification. Our findings indicate that, by altering phytoplankton community composition, this causal relationship may lead to a decreased efficiency of the biological pump in sequestering atmospheric CO2, implying a positive feedback in the climate system. These results provide a mechanistic basis for understanding the connection between upper ocean dynamics, the calcium carbonate-to-organic C production ratio and atmospheric pCO2 variations on time scales ranging from seasonal cycles to geological transitions. PMID:19075222

Toward Reducing Uncertainties in Biospheric Carbon Uptake in the American West: An Atmospheric Perspective

NASA Astrophysics Data System (ADS)

Lin, J. C.; Stephens, B. B.; Mallia, D.; Wu, D.; Jacobson, A. R.

2015-12-01

Despite the need for an understanding of terrestrial biospheric carbon fluxes to account for carbon cycle feedbacks and predict future CO2 concentrations, knowledge of such fluxes at the regional scale remains poor. This is particularly true in mountainous areas, where lack of observations combined with difficulties in their interpretation lead to significant uncertainties. Yet mountainous regions are also where significant forest cover and biomass are found—areas that have the potential to serve as carbon sinks. In particular, understanding carbon fluxes in the American West is of critical importance for the U.S. carbon budget, as the large area and biomass indicate potential for carbon sequestration. However, disturbances such as drought, insect outbreak, and wildfires in this region can introduce significant perturbations to the carbon cycle and thereby affect the amount of carbon sequestered by vegetation in the Rockies. To date, there have been few atmospheric CO2 observations in the American Rockies due to a combination of difficulties associated with logistics and interpretation of the measurements in the midst of complex terrain. Among the few sites are those associated with NCAR's Regional Atmospheric Continuous CO2 Network in the Rocky Mountains (Rocky RACCOON). As CO2 observations in mountainous areas increase in the future, it is imperative that they can be properly interpreted to yield information about biospheric carbon fluxes. In this paper, we will present CO2 observations from RACCOON, along with atmospheric simulations that attempt to extract information about biospheric carbon fluxes in the Western U.S. from these observations. We show that atmospheric models can significantly misinterpret the CO2 observations, leading to large errors in the retrieved biospheric fluxes, due to erroneous atmospheric flows. Recommendations for ways to minimize such errors and properly link the CO2 concentrations to biospheric fluxes are discussed.

Potentiel des méthodes de séparation et stockage du CO2 dans la lutte contre l'effet de serreThe role of CO2 capture and sequestration in mitigation of climate change

NASA Astrophysics Data System (ADS)

Jean-Baptiste, Philippe; Ducroux, René

2003-06-01

Increasing atmospheric level of greenhouse gases are causing global warming and putting at risk the global climate system. The main anthropogenic greenhouse gas is CO 2. Technical solutions exist to reduce CO 2 emission and stabilise atmospheric CO 2 concentration, including energy saving and energy efficiency, switch to lower carbon content fuels like natural gas and to energy sources that operate with zero CO 2 emissions such as renewable or nuclear energy, enhance the natural sinks for CO 2 (forests, soils, etc.), and last but not least, sequester CO 2 from fossil fuels combustion. The purpose of this paper is to provide an overview of the technology and cost for capture and storage of CO 2. Some of the factors that will influence application, including environmental impact, cost and efficiency, are also discussed. Capturing CO 2 and storing it in underground geological reservoirs appears as the best environmentally acceptable option. It can be done with existing technology; however, substantial R&D is needed to improve available technology and to lower the cost. Applicable to large CO 2 emitting industrial facilities such as power plants, cement factories, steel industry, etc., which amount to more than 30% of the global anthropogenic CO 2 emission, it represents a valuable tool in the battle against global warming. To cite this article: P. Jean-Baptiste, R. Ducroux, C. R. Geoscience 335 (2003).

Modeling the transformation of atmospheric CO2 into microalgal biomass.

PubMed

Hasan, Mohammed Fahad; Vogt, Frank

2017-10-23

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

Seasonal Changes in Plankton Food Web Structure and Carbon Dioxide Flux from Southern California Reservoirs

PubMed Central

Adamczyk, Emily M.; Shurin, Jonathan B.

2015-01-01

Reservoirs around the world contribute to cycling of carbon dioxide (CO2) with the atmosphere, but there is little information on how ecosystem processes determine the absorption or emission of CO2. Reservoirs are the most prevalent freshwater systems in the arid southwest of North America, yet it is unclear whether they sequester or release CO2 and therefore how water impoundment impacts global carbon cycling. We sampled three reservoirs in San Diego, California, weekly for one year. We measured seasonal variation in the abundances of bacteria, phytoplankton, and zooplankton, as well as water chemistry (pH, nutrients, ions, dissolved organic carbon [DOC]), which were used to estimate partial pressure of CO2 (pCO2), and CO2 flux. We found that San Diego reservoirs are most often undersaturated with CO2 with respect to the atmosphere and are estimated to absorb on average 3.22 mmol C m-2 day-1. pCO2 was highest in the winter and lower in the summer, indicating seasonal shifts in the magnitudes of photosynthesis and respiration associated with day length, temperature and water inputs. Abundances of microbes (bacteria) peaked in the winter along with pCO2, while phytoplankton, nutrients, zooplankton and DOC were all unrelated to pCO2. Our data indicate that reservoirs of semi-arid environments may primarily function as carbon sinks, and that carbon flux varies seasonally but is unrelated to nutrient or DOC availability, or the abundances of phytoplankton or zooplankton. PMID:26473601

The issues of energy and carbon cycle: new perspectives for assessing the environmental impact of animal waste utilization.

PubMed

Ceotto, E

2005-01-01

This paper focuses on the benefits of an efficient use of animal waste from the standpoint of curbing the rise of anthropogenic carbon dioxide (CO(2)) in the atmosphere. An effective use of animal waste resources might provide a partial, but still important, contribution in reducing net CO(2) emissions. In particular: the fulfillment of nutrient requirements of crop plants growing in non-limiting conditions and thus sequestering CO(2) at their potential level; the chance of diminishing the use of fossil energy, and related CO(2) emissions, required for manufacturing industrial fertilizers; the possibility of enhancing carbon sequestration in agricultural soils by the application of farmyard manure. The future success of agriculture in providing these ecosystem services can only be achieved with a changed social awareness of the links between sustainable land use and global environmental change.

An Analysis of the Climate Change Mitigation Potential through Soil Organic Carbon Sequestration in a Corn Belt Watershed

NASA Astrophysics Data System (ADS)

Bhattarai, M. D.; Secchi, S.; Schoof, J. T.

2015-12-01

The sequestration of carbon constitutes one of major options in agricultural climate change land-based mitigation. We examined the carbon sequestration potential of alternative agricultural land uses in an intensively farmed Corn Belt watershed. We Used downscaled data from eight atmosphere-ocean general circulation models (AOGCMs) for a simulation period between 2015 and 2099 with three emission pathways reflecting low, medium and high greenhouse gas scenarios. The use of downscaled data, coupled with high resolution land use and soil data, can help policy makers and land managers better understand spatial and temporal impacts of climate change. We consider traditional practices such as no-till corn-soybean rotations and continuous corn and include also switchgrass, a bioenergy crop. Our results show that switching from conventional tillage continuous corn to no-till corn-soybean can sequester the equivalent of 156,000 MtCO2 of soil organic carbon with a sequestration rate of 2.38 MtCO2 ha-1 yr-1 for the simulated period. Our results also indicate that switchgrass can sequester the equivalent of 282,000 MtCO2 of soil organic carbon with a sequestration rate of 4.4 MtCO2 ha-1 yr-1 for the period. Our finding also suggests that while climate change impacts corn and soybean yields, it does not have a significant effect on switchgrass yields possibly due to carbon fertilization effect on switchgrass yields.

Efficiency of small scale carbon mitigation by patch iron fertilization

NASA Astrophysics Data System (ADS)

Sarmiento, J. L.; Slater, R. D.; Dunne, J.; Gnanadesikan, A.; Hiscock, M. R.

2010-11-01

While nutrient depletion scenarios have long shown that the high-latitude High Nutrient Low Chlorophyll (HNLC) regions are the most effective for sequestering atmospheric carbon dioxide, recent simulations with prognostic biogeochemical models have suggested that only a fraction of the potential drawdown can be realized. We use a global ocean biogeochemical general circulation model developed at GFDL and Princeton to examine this and related issues. We fertilize two patches in the North and Equatorial Pacific, and two additional patches in the Southern Ocean HNLC region north of the biogeochemical divide and in the Ross Sea south of the biogeochemical divide. We evaluate the simulations using observations from both artificial and natural iron fertilization experiments at nearby locations. We obtain by far the greatest response to iron fertilization at the Ross Sea site, where sea ice prevents escape of sequestered CO2 during the wintertime, and the CO2 removed from the surface ocean by the biological pump is carried into the deep ocean by the circulation. As a consequence, CO2 remains sequestered on century time-scales and the efficiency of fertilization remains almost constant no matter how frequently iron is applied as long as it is confined to the growing season. The second most efficient site is in the Southern Ocean. The North Pacific site has lower initial nutrients and thus a lower efficiency. Fertilization of the Equatorial Pacific leads to an expansion of the suboxic zone and a striking increase in denitrification that causes a sharp reduction in overall surface biological export production and CO2 uptake. The impacts on the oxygen distribution and surface biological export are less prominent at other sites, but nevertheless still a source of concern. The century time scale retention of iron in this model greatly increases the long-term biological response to iron addition as compared with simulations in which the added iron is rapidly scavenged from the ocean.

The abiotically driven biological pump in the ocean and short-term fluctuations in atmospheric CO 2 contents

NASA Astrophysics Data System (ADS)

Ittekkot, Venugopalan

1993-07-01

Current debates on the significance of the oceanic "biological pump" in the removal of atmospheric CO 2 pay more attention to the act of biological carbon-dioxide fixation (primary productivity) in the sea, but pay less or no attention to the equally relevant aspect of the transfer of the fixed carbon to a sink before its oxidation back to CO 2. The upper ocean obviously disqualifies as a sink for biologically fixed CO 2 because of gas-exchange with the atmosphere. The deep ocean, on the other hand, can be a sink at least at time scales of the ocean turnover. Transfer of newly-fixed CO 2 to the deep sea can be accelerated by abiogenic matter introduced to the sea surface from terrestrial sources. This matter acts as ballast and increases the density and settling rates of aggregates of freshly synthesized organic matter thereby facilitating their rapid removal from the upper ocean. Higher supply of abiogenic matter enhances the sequestering of fresh organic matter and in effect shifts the zone of organic matter remineralization from the upper ocean to the deep sea. Consistent with this abiogenic forcing, the rate of organic matter remineralization and the subsequent storage of the remineralized carbon in the deep sea are linked to bulk fluxes (mass accumulation rates) in the deep sea. This mechanism acts as an "abiotic boost" in the workings of the oceanic "biological pump" and results in an increase in deep sea carbon storage; the magnitude of carbon thus stored could have caused the observed short term fluctuations in atmospheric CO 2-contents during the glacial-interglacial cycles.

Is the northern high latitude land-based CO2 sink weakening?

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

Mcguire, David; Kicklighter, David W.; Gurney, Kevin R

2011-01-01

Studies indicate that, historically, terrestrial ecosystems of the northern high latitude region may have been responsible for up to 60% of the global net land-based sink for atmospheric CO2. However, these regions have recently experienced remarkable modification of the major driving forces of the carbon cycle, including surface air temperature warming that is significantly greater than the global average and associated increases in the frequency and severity of disturbances. Whether arctic tundra and boreal forest ecosystems will continue to sequester atmospheric CO2 in the face of these dramatic changes is unknown. Here we show the results of model simulations thatmore » estimate a 41 Tg C yr-1 sink in the boreal land regions from 1997 to 2006, which represents a 73% reduction in the strength of the sink estimated for previous decades in the late 20th Century. Our results suggest that CO2 uptake by the region in previous decades may not be as strong as previously estimated. The recent decline in sink strength is the combined result of 1) weakening sinks due to warming-induced increases in soil organic matter decomposition and 2) strengthening sources from pyrogenic CO2 emissions as a result of the substantial area of boreal forest burned in wildfires across the region in recent years. Such changes create positive feedbacks to the climate system that accelerate global warming, putting further pressure on emission reductions to achieve atmospheric stabilization targets.« less

Is the northern high-latitude land-based CO2 sink weakening?

USGS Publications Warehouse

Hayes, D.J.; McGuire, A.D.; Kicklighter, D.W.; Gurney, K.R.; Burnside, T.J.; Melillo, J.M.

2011-01-01

Studies indicate that, historically, terrestrial ecosystems of the northern high-latitude region may have been responsible for up to 60% of the global net land-based sink for atmospheric CO2. However, these regions have recently experienced remarkable modification of the major driving forces of the carbon cycle, including surface air temperature warming that is significantly greater than the global average and associated increases in the frequency and severity of disturbances. Whether Arctic tundra and boreal forest ecosystems will continue to sequester atmospheric CO2 in the face of these dramatic changes is unknown. Here we show the results of model simulations that estimate a 41 Tg C yr-1 sink in the boreal land regions from 1997 to 2006, which represents a 73% reduction in the strength of the sink estimated for previous decades in the late 20th century. Our results suggest that CO 2 uptake by the region in previous decades may not be as strong as previously estimated. The recent decline in sink strength is the combined result of (1) weakening sinks due to warming-induced increases in soil organic matter decomposition and (2) strengthening sources from pyrogenic CO2 emissions as a result of the substantial area of boreal forest burned in wildfires across the region in recent years. Such changes create positive feedbacks to the climate system that accelerate global warming, putting further pressure on emission reductions to achieve atmospheric stabilization targets. Copyright 2011 by the American Geophysical Union.

Reactive transport modeling of CO2 mineral sequestration in basaltic rocks

NASA Astrophysics Data System (ADS)

Aradottir, E. S.; Sonnenthal, E. L.; Bjornsson, G.; Jonsson, H.

2011-12-01

CO2 mineral sequestration in basalt may provide a long lasting, thermodynamically stable, and environmentally benign solution to reduce greenhouse gases in the atmosphere. Multi-dimensional, field scale, reactive transport models of this process have been developed with a focus on the CarbFix pilot CO2 injection in Iceland. An extensive natural analog literature review was conducted in order to identify the primary and secondary minerals associated with water-basalt interaction at low and elevated CO2 conditions. Based on these findings, an internally consistent thermodynamic database describing the mineral reactions of interest was developed and validated. Hydrological properties of field scale mass transport models were properly defined by calibration to field data using iTOUGH2. Reactive chemistry was coupled to the models and TOUGHREACT used for running predictive simulations carried out with the objective of optimizing long-term management of injection sites, to quantify the amount of CO2 that can be mineralized, and to identify secondary minerals that compete with carbonates for cations leached from the primary rock. Calibration of field data from the CarbFix reservoir resulted in a horizontal permeability for lava flows of 300 mD and a vertical permeability of 1700 mD. Active matrix porosity was estimated to be 8.5%. The CarbFix numerical models were a valuable engineering tool for designing optimal injection and production schemes aimed at increasing groundwater flow. Reactive transport simulations confirm dissolution of primary basaltic minerals as well as carbonate formation, and thus indicate in situ CO2 mineral sequestration in basalts to be a viable option. Furthermore, the simulations imply that clay minerals are most likely to compete with magnesite-siderite solid solutions for Mg and Fe leached from primary minerals, whereas zeolites compete with calcite for dissolved Ca. In the case of the CarbFix pilot injection, which involves a continuous injection of 1,100 tons CO2 in total for 6 months, the basalt hosted reservoir was estimated to have a 100% sequestering efficiency after 10 years. In the case of an upscaled 10 year long injection of 40,000 tons per year, sequestering efficiency of the same reservoir was estimated to be about 10% after 100 years. However, sequestering efficiency in the latter case has every potential of increasing substantially with time due to the vast amount of primary basaltic minerals in the reservoir.

Method for reducing CO2, CO, NOX, and SOx emissions

DOEpatents

Lee, James Weifu; Li, Rongfu

2002-01-01

Industrial combustion facilities are integrated with greenhouse gas-solidifying fertilizer production reactions so that CO.sub.2, CO, NO.sub.x, and SO.sub.x emissions can be converted prior to emission into carbonate-containing fertilizers, mainly NH.sub.4 HCO.sub.3 and/or (NH.sub.2).sub.2 CO, plus a small fraction of NH.sub.4 NO.sub.3 and (NH.sub.4).sub.2 SO.sub.4. The invention enhances sequestration of CO.sub.2 into soil and the earth subsurface, reduces N0.sub.3.sup.- contamination of surface and groundwater, and stimulates photosynthetic fixation of CO.sub.2 from the atmosphere. The method for converting CO.sub.2, CO, NO.sub.x, and SO.sub.x emissions into fertilizers includes the step of collecting these materials from the emissions of industrial combustion facilities such as fossil fuel-powered energy sources and transporting the emissions to a reactor. In the reactor, the CO.sub.2, CO, N.sub.2, SO.sub.x, and/or NO.sub.x are converted into carbonate-containing fertilizers using H.sub.2, CH.sub.4, or NH.sub.3. The carbonate-containing fertilizers are then applied to soil and green plants to (1) sequester inorganic carbon into soil and subsoil earth layers by enhanced carbonation of groundwater and the earth minerals, (2) reduce the environmental problem of NO.sub.3.sup.- runoff by substituting for ammonium nitrate fertilizer, and (3) stimulate photosynthetic fixation of CO.sub.2 from the atmosphere by the fertilization effect of the carbonate-containing fertilizers.

A Sea Floor Gravity Survey of the Sleipner Field to Monitor CO2 Migration

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

Mark Zumberge

Carbon dioxide gas (CO{sub 2}) is a byproduct of many wells that produce natural gas. Frequently the CO{sub 2} separated from the valuable fossil fuel gas is released into the atmosphere. This adds to the growing problem of the climatic consequences of greenhouse gas contamination. In the Sleipner North Sea natural gas production facility, the separated CO{sub 2} is injected into an underground saline aquifer to be forever sequestered. Monitoring the fate of such sequestered material is important - and difficult. Local change in Earth's gravity field over the injected gas is one way to detect the CO{sub 2} andmore » track its migration within the reservoir over time. The density of the injected gas is less than that of the brine that becomes displaced from the pore space of the formation, leading to slight but detectable decrease in gravity observed on the seafloor above the reservoir. Using equipment developed at Scripps Institution of Oceanography, we have been monitoring gravity over the Sleipner CO{sub 2} sequestration reservoir since 2002. We surveyed the field in 2009 in a project jointly funded by a consortium of European oil and gas companies and the US Department of Energy. The value of gravity at some 30 benchmarks on the seafloor, emplaced at the beginning of the monitoring project, was observed in a week-long survey with a remotely operated vehicle. Three gravity meters were deployed on the benchmarks multiple times in a campaign-style survey, and the measured gravity values compared to those collected in earlier surveys. A clear signature in the map of gravity differences is well correlated with repeated seismic surveys.« less

Carbon dioxide emission from bamboo culms.

PubMed

Zachariah, E J; Sabulal, B; Nair, D N K; Johnson, A J; Kumar, C S P

2016-05-01

Bamboos are one of the fastest growing plants on Earth, and are widely considered to have high ability to capture and sequester atmospheric carbon, and consequently to mitigate climate change. We tested this hypothesis by measuring carbon dioxide (CO2 ) emissions from bamboo culms and comparing them with their biomass sequestration potential. We analysed diurnal effluxes from Bambusa vulgaris culm surface and gas mixtures inside hollow sections of various bamboos using gas chromatography. Corresponding variations in gas pressure inside the bamboo section and culm surface temperature were measured. SEM micrographs of rhizome and bud portions of bamboo culms were also recorded. We found very high CO2 effluxes from culm surface, nodes and buds of bamboos. Positive gas pressure and very high concentrations of CO2 were observed inside hollow sections of bamboos. The CO2 effluxes observed from bamboos were very high compared to their carbon sequestration potential. Our measurements suggest that bamboos are net emitters of CO2 during their lifespan. © 2016 German Botanical Society and The Royal Botanical Society of the Netherlands.

Efficiency of small scale carbon mitigation by patch iron fertilization

NASA Astrophysics Data System (ADS)

Sarmiento, J. L.; Slater, R. D.; Dunne, J.; Gnanadesikan, A.; Hiscock, M. R.

2009-11-01

While nutrient depletion scenarios have long shown that the high-latitude High Nutrient Low Chlorophyll (HNLC) regions are the most effective for sequestering atmospheric carbon dioxide, recent simulations with prognostic biogeochemical models have suggested that only a fraction of the potential drawdown can be realized. We use a global ocean biogeochemical general circulation model developed at GFDL and Princeton to examine this and related issues. We fertilize two patches in the North and Equatorial Pacific, and two additional patches in the Southern Ocean HNLC region north of the biogeochemical divide and in the Ross Sea south of the biogeochemical divide. We obtain by far the greatest response to iron fertilization at the Ross Sea site. Here the CO2 remains sequestered on century time-scales and the efficiency of fertilization remains almost constant no matter how frequently iron is applied as long as it is confined to the growing season. The second most efficient site is in the Southern Ocean. Here the biological response to iron fertilization is comparable to the Ross Sea, but the enhanced biological uptake of CO2 is more spread out in the vertical and thus less effective at leading to removal of CO2 from the atmosphere. The North Pacific site has lower initial nutrients and thus a lower efficiency. Fertilization of the Equatorial Pacific leads to an expansion of the suboxic zone and a striking increase in denitrification that causes a sharp reduction in overall surface biological export production and CO2 uptake. The impacts on the oxygen distribution and surface biological export are less prominent at other sites, but nevertheless still a source of concern. The century time scale retention of iron in these models greatly increases the long-term biological response to iron addition as compared with models in which the added iron is rapidly scavenged from the ocean.

The Efficacy and Potential of Renewable Energy from Carbon Dioxide that is Sequestered in Sedimentary Basin Geothermal Resources

NASA Astrophysics Data System (ADS)

Bielicki, J. M.; Adams, B. M.; Choi, H.; Saar, M. O.; Taff, S. J.; Jamiyansuren, B.; Buscheck, T. A.; Ogland-Hand, J.

2015-12-01

Mitigating climate change requires increasing the amount of electricity that is generated from renewable energy technologies and while simultaneously reducing the amount of carbon dioxide (CO2) that is emitted to the atmosphere from present energy and industrial facilities. We investigated the efficacy of generating electricity using renewable geothermal heat that is extracted by CO2 that is sequestered in sedimentary basins. To determine the efficacy of CO2-Geothermal power production in the United States, we conducted a geospatial resource assessment of the combination of subsurface CO2 storage capacity and heat flow in sedimentary basins and developed an integrated systems model that combines reservoir modeling with power plant modeling and economic costs. The geospatial resource assessment estimates the potential resource base for CO2-Geothermal power plants, and the integrated systems model estimates the physical (e.g., net power) and economic (e.g., levelized cost of electricity, capital cost) performance of an individual CO2-Geothermal power plant for a range of reservoir characteristics (permeability, depth, geothermal temperature gradient). Using coupled inverted five-spot injection patterns that are common in CO2-enhanced oil recovery operations, we determined the well pattern size that best leveraged physical and economic economies of scale for the integrated system. Our results indicate that CO2-Geothermal plants can be cost-effectively deployed in a much larger region of the United States than typical approaches to geothermal electricity production. These cost-effective CO2-Geothermal electricity facilities can also be capacity-competitive with many existing baseload and renewable energy technologies over a range of reservoir parameters. For example, our results suggest that, given the right combination of reservoir parameters, LCOEs can be as low as $25/MWh and capacities can be as high as a few hundred MW.

Key role of symbiotic dinitrogen fixation in tropical forest secondary succession

NASA Astrophysics Data System (ADS)

Batterman, Sarah A.; Hedin, Lars O.; van Breugel, Michiel; Ransijn, Johannes; Craven, Dylan J.; Hall, Jefferson S.

2013-10-01

Forests contribute a significant portion of the land carbon sink, but their ability to sequester CO2 may be constrained by nitrogen, a major plant-limiting nutrient. Many tropical forests possess tree species capable of fixing atmospheric dinitrogen (N2), but it is unclear whether this functional group can supply the nitrogen needed as forests recover from disturbance or previous land use, or expand in response to rising CO2 (refs 6, 8). Here we identify a powerful feedback mechanism in which N2 fixation can overcome ecosystem-scale deficiencies in nitrogen that emerge during periods of rapid biomass accumulation in tropical forests. Over a 300-year chronosequence in Panama, N2-fixing tree species accumulated carbon up to nine times faster per individual than their non-fixing neighbours (greatest difference in youngest forests), and showed species-specific differences in the amount and timing of fixation. As a result of fast growth and high fixation, fixers provided a large fraction of the nitrogen needed to support net forest growth (50,000kg carbon per hectare) in the first 12years. A key element of ecosystem functional diversity was ensured by the presence of different N2-fixing tree species across the entire forest age sequence. These findings show that symbiotic N2 fixation can have a central role in nitrogen cycling during tropical forest stand development, with potentially important implications for the ability of tropical forests to sequester CO2.

Key role of symbiotic dinitrogen fixation in tropical forest secondary succession.

PubMed

Batterman, Sarah A; Hedin, Lars O; van Breugel, Michiel; Ransijn, Johannes; Craven, Dylan J; Hall, Jefferson S

2013-10-10

Forests contribute a significant portion of the land carbon sink, but their ability to sequester CO2 may be constrained by nitrogen, a major plant-limiting nutrient. Many tropical forests possess tree species capable of fixing atmospheric dinitrogen (N2), but it is unclear whether this functional group can supply the nitrogen needed as forests recover from disturbance or previous land use, or expand in response to rising CO2 (refs 6, 8). Here we identify a powerful feedback mechanism in which N2 fixation can overcome ecosystem-scale deficiencies in nitrogen that emerge during periods of rapid biomass accumulation in tropical forests. Over a 300-year chronosequence in Panama, N2-fixing tree species accumulated carbon up to nine times faster per individual than their non-fixing neighbours (greatest difference in youngest forests), and showed species-specific differences in the amount and timing of fixation. As a result of fast growth and high fixation, fixers provided a large fraction of the nitrogen needed to support net forest growth (50,000 kg carbon per hectare) in the first 12 years. A key element of ecosystem functional diversity was ensured by the presence of different N2-fixing tree species across the entire forest age sequence. These findings show that symbiotic N2 fixation can have a central role in nitrogen cycling during tropical forest stand development, with potentially important implications for the ability of tropical forests to sequester CO2.

Carbon Dioxide Emissions Associated with the Restoration of a Tidal Salt Marsh in Boston, MA

NASA Astrophysics Data System (ADS)

Bulpett, K.; Chen, R. F.

2016-02-01

Decades of land alterations had led to the encroachment of the invasive Phragmites australis in the Neponset River salt marshes in Boston, Massachusetts. An 11 acre area on the west bank of the Neponset River had been underlain by dredge spoil and was several feet higher in elevation than surrounding marsh; contributing to the domination of Phragmites which occurred at high enough densities to virtually exclude native vegetation species and posed as an ecological threat to the remaining marshlands. In 2005, restoration of this section involved excavating approximately 46,700 cubic yards of dredged materials; effectively lowering the marsh platform by 1.5 feet to reestablish tidal flushing. The removed materials were relocated to an area deemed unlikely for future restoration efforts on the northern portion of the site, containing relatively high elevations from previous dredge spoil deposits and dense strands of Phragmites. The mitigation has been considered successful as seawater inundation has promoted the replacement of the Phragmites with native Spartina alterniflora. The excavation and relocation of dredge materials exposed previously buried marsh sediments to the atmosphere. Our research study focuses on determining how much carbon dioxide (CO2) may have been released due to the disturbance of this sequestered carbon. Ten years after the restoration, in 2015, direct measurements of CO2 fluxes from the soils in the remediated site, an unrestored area, and the dredge spoils reveal differing CO2 emission rates between the three sites, measuring at 1.54 ± 0.70 μmol/m2/s, 5.48 ± 2.68 μmol/m2/s, 9.57 ± 2.09 μmol/m2/s respectively. Our measurements suggest that the restoration has resulted in a significant release of previously sequestered carbon to the atmosphere. Estimations of potential emissions and avoided emissions resulting from coastal restoration projects are necessary in evaluating mitigation policies and practices and managing conservation efforts of these essential ecosystems.

Integrating Algae with Bioenergy Carbon Capture and Storage (ABECCS) Increases Sustainability

NASA Astrophysics Data System (ADS)

Beal, Colin M.; Archibald, Ian; Huntley, Mark E.; Greene, Charles H.; Johnson, Zackary I.

2018-03-01

Bioenergy carbon capture and storage (BECCS) has been proposed to reduce atmospheric CO2 concentrations, but concerns remain about competition for arable land and freshwater. The synergistic integration of algae production, which does not require arable land or freshwater, with BECCS (called "ABECCS") can reduce CO2 emissions without competing with agriculture. This study presents a technoeconomic and life-cycle assessment for colocating a 121-ha algae facility with a 2,680-ha eucalyptus forest for BECCS. The eucalyptus biomass fuels combined heat and power (CHP) generation with subsequent amine-based carbon capture and storage (CCS). A portion of the captured CO2 is used for growing algae and the remainder is sequestered. Biomass combustion supplies CO2, heat, and electricity, thus increasing the range of sites suitable for algae cultivation. Economic, energetic, and environmental impacts are considered. The system yields as much protein as soybeans while generating 61.5 TJ of electricity and sequestering 29,600 t of CO2 per year. More energy is generated than consumed and the freshwater footprint is roughly equal to that for soybeans. Financial break-even is achieved for product value combinations that include 1) algal biomass sold for 1,400/t (fishmeal replacement) with a 68/t carbon credit and 2) algal biomass sold for 600/t (soymeal replacement) with a 278/t carbon credit. Sensitivity analysis shows significant reductions to the cost of carbon sequestration are possible. The ABECCS system represents a unique technology for negative emissions without reducing protein production or increasing water demand, and should therefore be included in the suite of technologies being considered to address global sustainability.

Geochemical monitoring for potential environmental impacts of geologic sequestration of CO2

USGS Publications Warehouse

Kharaka, Yousif K.; Cole, David R.; Thordsen, James J.; Gans, Kathleen D.; Thomas, Randal B.

2013-01-01

Carbon dioxide sequestration is now considered an important component of the portfolio of options for reducing greenhouse gas emissions to stabilize their atmospheric levels at values that would limit global temperature increases to the target of 2 °C by the end of the century (Pacala and Socolow 2004; IPCC 2005, 2007; Benson and Cook 2005; Benson and Cole 2008; IEA 2012; Romanak et al. 2013). Increased anthropogenic emissions of CO2 have raised its atmospheric concentrations from about 280 ppmv during pre-industrial times to ~400 ppmv today, and based on several defined scenarios, CO2 concentrations are projected to increase to values as high as 1100 ppmv by 2100 (White et al. 2003; IPCC 2005, 2007; EIA 2012; Global CCS Institute 2012). An atmospheric CO2 concentration of 450 ppmv is generally the accepted level that is needed to limit global temperature increases to the target of 2 °C by the end of the century. This temperature limit likely would moderate the adverse effects related to climate change that could include sea-level rise from the melting of alpine glaciers and continental ice sheets and from the ocean warming; increased frequency and intensity of wildfires, floods, droughts, and tropical storms; and changes in the amount, timing, and distribution of rain, snow, and runoff (IPCC 2007; Sundquist et al. 2009; IEA 2012). Rising atmospheric CO2 concentrations are also increasing the amount of CO2 dissolved in ocean water lowering its pH from 8.1 to 8.0, with potentially disruptive effects on coral reefs, plankton and marine ecosystems (Adams and Caldeira 2008; Schrag 2009; Sundquist et al. 2009). Sedimentary basins in general and deep saline aquifers in particular are being investigated as possible repositories for the large volumes of anthropogenic CO2 that must be sequestered to mitigate global warming and related climate changes (Hitchon 1996; Benson and Cole 2008; Verma and Warwick 2011).

Potential for the Use of Wireless Sensor Networks for Monitoring of CO2 Leakage Risks

NASA Astrophysics Data System (ADS)

Pawar, R.; Illangasekare, T. H.; Han, Q.; Jayasumana, A.

2015-12-01

Storage of supercritical CO2 in deep saline geologic formation is under study as a means to mitigate potential global climate change from green house gas loading to the atmosphere. Leakage of CO2 from these formations poses risk to the storage permanence goal of 99% of injected CO2 remaining sequestered from the atmosphere,. Leaked CO2 that migrates into overlying groundwater aquifers may cause changes in groundwater quality that pose risks to environmental and human health. For these reasons, technologies for monitoring, measuring and accounting of injected CO2 are necessary for permitting of CO2 sequestration projects under EPA's class VI CO2 injection well regulations. While the probability of leakage related to CO2 injection is thought to be small at characterized and permitted sites, it is still very important to protect the groundwater resources and develop methods that can efficiently and accurately detect CO2 leakage. Methods that have been proposed for leakage detection include remote sensing, soil gas monitoring, geophysical techniques, pressure monitoring, vegetation stress and eddy covariance measurements. We have demonstrated the use of wireless sensor networks (WSN) for monitoring of subsurface contaminant plumes. The adaptability of this technology for leakage monitoring of CO2 through geochemical changes in the shallow subsurface is explored. For this technology to be viable, it is necessary to identify geochemical indicators such as pH or electrical conductivity that have high potential for significant change in groundwater in the event of CO2 leakage. This talk presents a conceptual approach to use WSNs for CO2 leakage monitoring. Based on our past work on the use of WSN for subsurface monitoring, some of the challenges that need to be over come for this technology to be viable for leakage detection will be discussed.

Long Time Evolution of Sequestered CO2 in Porous Media

NASA Astrophysics Data System (ADS)

Cohen, Y.; Rothman, D.

2013-12-01

CO2 sequestration is important for mitigating climate change and reducing atmospheric CO2 concentration. However, a complete physical picture able to predict both the pattern formation and the structure developing within the porous medium is lacking. We propose a theoretical model that couples transport, reaction, and the intricate geometry of the rock, in order to study the long time evolution of carbon in the brine-rock environment. As CO2 is injected into a brine-rock environment, it becomes initially trapped, and isolated bubbles are formed. Within the high CO2 phase, minerals dissolve and migrate from high concentration to low concentration regions, along with other carbonate species. The change in the concentrations at the interface moves the system out of equilibrium, drives up the saturation level, and leads to mineral precipitation. We argue that mineral precipitation in a small boundary layer may lead to lower diffusivity, slower kinetics, and eventually to a mechanical trapping of the CO2 bubbles. We investigate the reactive transport model and study the conditions that cause the mechanical separation of these two reactive fluids in porous media.

A review of mineral carbonation technologies to sequester CO2.

PubMed

Sanna, A; Uibu, M; Caramanna, G; Kuusik, R; Maroto-Valer, M M

2014-12-07

Carbon dioxide (CO2) capture and sequestration includes a portfolio of technologies that can potentially sequester billions of tonnes of CO2 per year. Mineral carbonation (MC) is emerging as a potential CCS technology solution to sequester CO2 from smaller/medium emitters, where geological sequestration is not a viable option. In MC processes, CO2 is chemically reacted with calcium- and/or magnesium-containing materials to form stable carbonates. This work investigates the current advancement in the proposed MC technologies and the role they can play in decreasing the overall cost of this CO2 sequestration route. In situ mineral carbonation is a very promising option in terms of resources available and enhanced security, but the technology is still in its infancy and transport and storage costs are still higher than geological storage in sedimentary basins ($17 instead of $8 per tCO2). Ex situ mineral carbonation has been demonstrated on pilot and demonstration scales. However, its application is currently limited by its high costs, which range from $50 to $300 per tCO2 sequestered. Energy use, the reaction rate and material handling are the key factors hindering the success of this technology. The value of the products seems central to render MC economically viable in the same way as conventional CCS seems profitable only when combined with EOR. Large scale projects such as the Skyonic process can help in reducing the knowledge gaps on MC fundamentals and provide accurate costing and data on processes integration and comparison. The literature to date indicates that in the coming decades MC can play an important role in decarbonising the power and industrial sector.

White Mars: A New Model for Mars' Surface and Atmosphere Based on CO 2

NASA Astrophysics Data System (ADS)

Hoffman, Nick

2000-08-01

A new model is presented for the Amazonian outburst floods on Mars. Rather than the working fluid being water, with the associated difficulties in achieving warm and wet conditions on Mars and on collecting and removing the water before and after the floods, instead this model suggests that CO 2 is the active agent in the "floods." The flow is not a conventional liquid flood but is instead a gas-supported density flow akin to terrestrial volcanic pyroclastic flows and surges and at cryogenic temperatures with support from degassing of CO 2-bearing ices. The flows are not sourced from volcanic vents, but from the collapse of thick layered regolith containing liquid CO 2 to form zones of chaotic terrain, as shown by R. St. J. Lambert and V. E. Chamberlain (1978, Icarus34, 568-580; 1992, Workshop on the Evolution of the Martian Atmosphere). Submarine turbidites are also analagous in the flow mechanism, but the martian cryogenic flows were both dry and subaerial, so there is no need for a warm and wet epoch nor an ocean on Mars. Armed with this new model for the floods we review the activity of volatiles on the surface of Mars in the context of a cold ice world—"White Mars." We find that many of the recognized paradoxes about Mars' surface and atmosphere are resolved. In particular, the lack of carbonates on Mars is due to the lack of liquid water. The CO 2 of the primordial atmosphere and the H 2O inventory remain largely sequestered in subsurface ices. The distribution of water ice on modern Mars is also reevaluated, with important potential consequences for future Mars exploration. The model for collapse of terrain due to ices that show decompression melting, and the generation of nonaqueous flows in these circumstances may also be applicable to outer Solar System bodies, where CO 2, SO 2, N 2, and other ices are stable.

Phylogenetic variation of phytolith carbon sequestration in bamboos

PubMed Central

Li, Beilei; Song, Zhaoliang; Li, Zimin; Wang, Hailong; Gui, Renyi; Song, Ruisheng

2014-01-01

Phytoliths, the amorphous silica deposited in plant tissues, can occlude organic carbon (phytolith-occluded carbon, PhytOC) during their formation and play a significant role in the global carbon balance. This study explored phylogenetic variation of phytolith carbon sequestration in bamboos. The phytolith content in bamboo varied substantially from 4.28% to 16.42%, with the highest content in Sasa and the lowest in Chimonobambusa, Indocalamus and Acidosasa. The mean PhytOC production flux and rate in China's bamboo forests were 62.83 kg CO2 ha−1 y−1 and 4.5 × 108 kg CO2 y−1, respectively. This implies that 1.4 × 109 kg CO2 would be sequestered in world's bamboo phytoliths because the global bamboo distribution area is about three to four times higher than China's bamboo. Therefore, both increasing the bamboo area and selecting high phytolith-content bamboo species would increase the sequestration of atmospheric CO2 within bamboo phytoliths. PMID:24736571

Elution of Uranium and Transition Metals from Amidoxime-Based Polymer Adsorbents for Sequestering Uranium from Seawater

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

Pan, Horng-Bin; Kuo, Li-Jung; Wai, Chien M.

2015-11-30

High-surface-area amidoxime and carboxylic acid grafted polymer adsorbents developed at Oak Ridge National Laboratory were tested for sequestering uranium in a flowing seawater flume system at the PNNL-Marine Sciences Laboratory. FTIR spectra indicate that a KOH conditioning process is necessary to remove the proton from the carboxylic acid and make the sorbent effective for sequestering uranium from seawater. The alkaline conditioning process also converts the amidoxime groups to carboxylate groups in the adsorbent. Both Na 2CO 3-H 2O 2 and hydrochloric acid elution methods can remove ~95% of the uranium sequestered by the adsorbent after 42 days of exposure inmore » real seawater. The Na 2CO 3-H 2O 2 elution method is more selective for uranium than conventional acid elution. Iron and vanadium are the two major transition metals competing with uranium for adsorption to the amidoxime-based adsorbents in real seawater.« less

Carbon dioxide efflux from soil with poultry litter applications in conventional and conservation tillage systems in northern Alabama.

PubMed

Roberson, T; Reddy, K C; Reddy, S S; Nyakatawa, E Z; Raper, R L; Reeves, D W; Lemunyon, J

2008-01-01

Increased CO2 release from soils resulting from agricultural practices such as tillage has generated concerns about contributions to global warming. Maintaining current levels of soil C and/or sequestering additional C in soils are important mechanisms to reduce CO2 in the atmosphere through production agriculture. We conducted a study in northern Alabama from 2003 to 2006 to measure CO2 efflux and C storage in long-term tilled and non-tilled cotton (Gossypium hirsutum L.) plots receiving poultry litter or ammonium nitrate (AN). Treatments were established in 1996 on a Decatur silt loam (clayey, kaolinitic thermic, Typic Paleudults) and consisted of conventional-tillage (CT), mulch-tillage (MT), and no-tillage (NT) systems with winter rye [Secale cereale (L.)] cover cropping and AN and poultry litter (PL) as nitrogen sources. Cotton was planted in 2003, 2004, and 2006. Corn was planted in 2005 as a rotation crop using a no-till planter in all plots, and no fertilizer was applied. Poultry litter application resulted in higher CO2 emission from soil compared with AN application regardless of tillage system. In 2003 and 2006, CT (4.39 and 3.40 micromol m(-2) s(-1), respectively) and MT (4.17 and 3.39 micromol m(-2) s(-1), respectively) with PL at 100 kg N ha(-1) (100 PLN) recorded significantly higher CO2 efflux compared with NT with 100 PLN (2.84 and 2.47 micromol m(-2) s(-1), respectively). Total soil C at 0- to 15-cm depth was not affected by tillage but significantly increased with PL application and winter rye cover cropping. In general, cotton produced with NT conservation tillage in conjunction with PL and winter rye cover cropping reduced CO2 emissions and sequestered more soil C compared with control treatments.

The Atmospheric Constraint: What we Know About the State of the Carbon Cycle by Observing Carbon Dioxide and Methane

NASA Astrophysics Data System (ADS)

Denning, S.; Jacobson, A. R.; Miller, J. B.; Ballantyne, A.; Bruhwiler, L.; Chatterjee, A.; Davis, K. J.; Duncan, B. N.; Gurney, K. R.; Houghton, R. A.; Keppel-Aleks, G.; Michalak, A. M.; Ott, L.

2016-12-01

Much of what is known about the global carbon cycle has been learned by studying the time rate of change and spatial distribution of carbon gases in the atmosphere. In the past decade, the network of measurements of atmospheric CO2 and CH4 has increased by leaps and bounds. Observations now include many programs of sample collection; commercial as well as academic and government measurement programs; in-situ measurements from towers, ships, and aircraft; and new satellite sensors with near-global coverage. Quantitative estimates of regional budgets for both CO2 and CH4 require atmospheric tracer transport inversion. These methods have been further developed and improved in recent years and several groups are now providing updated regional fluxes using a suite of such models. Analysis of atmospheric CO2 has shown that ongoing sink processes continue to sequester about half of global fossil fuel emissions, with about half the sink activity on land and half in the oceans. Enhanced observing and improved inverse modeling of CO2 has been evaluated for smaller regions and shown to match direct carbon inventories. Aircraft sampling and satellite observations have finally begun to converge on the partition between tropical and extratropical land sinks and on the influence of climate variability. Additional tracers such as 13CO2, 14CO2, and COS as well as new remote sensing products such as solar induced fluorescence are helping carbon cycle scientists to better understand and predict sink mechanisms. An emerging area of work is the use of atmospheric data to conduct monitoring, reporting, and verification of emissions from point sources and cities. A major field campaign to study CO2 transport by convective and frontal storms is now underway. After a period of stable concentrations, concentrations of atmospheric CH4 have again begun to increase. Campaigns using mobile instruments and in-situ measurements made from fixed towers have established that leakage of CH4 associated with oil and gas extraction is greater than had previously been estimated. A dedicated field campaigns to study CH4 sources in the Arctic have carefully quantified emissions from seasonal sources such as wetlands and forests as well as point sources.

Carbon balance of South Asia constrained by passenger aircraft CO2 measurements

NASA Astrophysics Data System (ADS)

Patra, P. K.; Niwa, Y.; Schuck, T. J.; Brenninkmeijer, C. A. M.; Machida, T.; Matsueda, H.; Sawa, Y.

2011-02-01

Quantifying the fluxes of carbon dioxide (CO2) between the atmosphere and terrestrial ecosystems in all their diversity, across the continents, is important and urgent for implementing effective mitigating policies. Whereas much is known for Europe and North America for instance, in comparison, South Asia, with 1.6 billion inhabitants and considerable CO2 fluxes, remained terra incognita in this respect. We use regional measurements of atmospheric CO2 aboard a Lufthansa passenger aircraft between Frankfurt (Germany) and Chennai (India) at cruise altitude, in addition to the existing network sites for 2008, to estimate monthly fluxes for 64-regions using Bayesian inversion and transport model simulations. The applicability of the model's transport parameterization is confirmed using SF6, CH4 and N2O simulations for the CARIBIC datasets. The annual carbon flux obtained by including the aircraft data is twice as large as the fluxes simulated by a terrestrial ecosystem model that was applied to prescribe the fluxes used in the inversions. It is shown that South Asia sequestered carbon at a rate of 0.37±0.20 Pg C yr-1 (1Pg C = 1015 g of carbon in CO2) for the years 2007 and 2008. The seasonality and the strength of the calculated monthly fluxes are successfully validated using independent measurements of vertical CO2 profiles over Delhi and spatial variations at cruising altitude over Asia aboard Japan Airlines passenger aircraft.

Carbon balance of South Asia constrained by passenger aircraft CO2 measurements

NASA Astrophysics Data System (ADS)

Patra, P. K.; Niwa, Y.; Schuck, T. J.; Brenninkmeijer, C. A. M.; Machida, T.; Matsueda, H.; Sawa, Y.

2011-05-01

Quantifying the fluxes of carbon dioxide (CO2) between the atmosphere and terrestrial ecosystems in all their diversity, across the continents, is important and urgent for implementing effective mitigating policies. Whereas much is known for Europe and North America for instance, in comparison, South Asia, with 1.6 billion inhabitants and considerable CO2 fluxes, remained terra incognita in this respect. We use regional measurements of atmospheric CO2 aboard a Lufthansa passenger aircraft between Frankfurt (Germany) and Chennai (India) at cruise altitude, in addition to the existing network sites for 2008, to estimate monthly fluxes for 64-regions using Bayesian inversion and transport model simulations. The applicability of the model's transport parameterization is confirmed using SF6, CH4 and N2O simulations for the CARIBIC datasets. The annual amplitude of carbon flux obtained by including the aircraft data is twice as large as the fluxes simulated by a terrestrial ecosystem model that was applied to prescribe the fluxes used in the inversions. It is shown that South Asia sequestered carbon at a rate of 0.37 ± 0.20 Pg C yr-1 (1 Pg C = 1015 g of carbon in CO2) for the years 2007 and 2008. The seasonality and the strength of the calculated monthly fluxes are successfully validated using independent measurements of vertical CO2 profiles over Delhi and spatial variations at cruising altitude over Asia aboard Japan Airlines passenger aircraft.

The Evolution of Deep Ocean Chemistry and Respired Carbon in the Eastern Equatorial Pacific Over the Last Deglaciation

NASA Astrophysics Data System (ADS)

de la Fuente, Maria; Calvo, Eva; Skinner, Luke; Pelejero, Carles; Evans, David; Müller, Wolfgang; Povea, Patricia; Cacho, Isabel

2017-12-01

It has been shown that the deep Eastern Equatorial Pacific (EEP) region was poorly ventilated during the Last Glacial Maximum (LGM) relative to Holocene values. This finding suggests a more efficient biological pump, which indirectly supports the idea of increased carbon storage in the deep ocean contributing to lower atmospheric CO2 during the last glacial. However, proxies related to respired carbon are needed in order to directly test this proposition. Here we present Cibicides wuellerstorfi B/Ca ratios from Ocean Drilling Program Site 1240 measured by laser ablation inductively coupled plasma mass spectrometry (LA-ICPMS) as a proxy for deep water carbonate saturation state (Δ[CO32-], and therefore [CO32-]), along with δ13C measurements. In addition, the U/Ca ratio in foraminiferal coatings has been analyzed as an indicator of oxygenation changes. Our results show lower [CO32-], δ13C, and [O2] values during the LGM, which would be consistent with higher respired carbon levels in the deep EEP driven, at least in part, by reduced deep water ventilation. However, the difference between LGM and Holocene [CO32-] observed at our site is relatively small, in accordance with other records from across the Pacific, suggesting that a "counteracting" mechanism, such as seafloor carbonate dissolution, also played a role. If so, this mechanism would have increased average ocean alkalinity, allowing even more atmospheric CO2 to be "sequestered" by the ocean. Therefore, the deep Pacific Ocean very likely stored a significant amount of atmospheric CO2 during the LGM, specifically due to a more efficient biological carbon pump and also an increase in average ocean alkalinity.

Non-volcanic CO2 Earth degassing: Case of Mefite d'Ansanto (southern Apennines), Italy

NASA Astrophysics Data System (ADS)

Chiodini, G.; Granieri, D.; Avino, R.; Caliro, S.; Costa, A.; Minopoli, C.; Vilardo, G.

2010-06-01

Mefite d'Ansanto, southern Apennines, Italy is the largest natural emission of low temperature CO2 rich gases, from non-volcanic environment, ever measured in the Earth. The emission is fed by a buried reservoir, made up of permeable limestones and covered by clayey sediments. We estimated a total gas flux of ˜2000 tons per day. Under low wind conditions, the gas flows along a narrow natural channel producing a persistent gas river which has killed over a period of time people and animals. The application of a physical numerical model allowed us to define the zones which potentially can be affected by dangerous CO2 concentration at breathing height for humans. The geometry of the Mefite gas reservoir is similar to those designed for sequestering CO2 in geological storage projects where huge amounts of CO2 should be injected in order to reduce atmospheric CO2 concentration. The approach which we have used at Mefite to define hazardous zones for the human health can be applied also in case of large CO2 leakages from storage sites, a phenomena which, even if improbable, can not be ruled out.

The key to commercial-scale geological CO2 sequestration: Displaced fluid management

USGS Publications Warehouse

Surdam, R.C.; Jiao, Z.; Stauffer, P.; Miller, T.

2011-01-01

The Wyoming State Geological Survey has completed a thorough inventory and prioritization of all Wyoming stratigraphic units and geologic sites capable of sequestering commercial quantities of CO2 (5-15 Mt CO 2/year). This multi-year study identified the Paleozoic Tensleep/Weber Sandstone and Madison Limestone (and stratigraphic equivalent units) as the leading clastic and carbonate reservoir candidates for commercial-scale geological CO2 sequestration in Wyoming. This conclusion was based on unit thickness, overlying low permeability lithofacies, reservoir storage and continuity properties, regional distribution patterns, formation fluid chemistry characteristics, and preliminary fluid-flow modeling. This study also identified the Rock Springs Uplift in southwestern Wyoming as the most promising geological CO2 sequestration site in Wyoming and probably in any Rocky Mountain basin. The results of the WSGS CO2 geological sequestration inventory led the agency and colleagues at the UW School of Energy Resources Carbon Management Institute (CMI) to collect available geologic, petrophysical, geochemical, and geophysical data on the Rock Springs Uplift, and to build a regional 3-D geologic framework model of the Uplift. From the results of these tasks and using the FutureGen protocol, the WSGS showed that on the Rock Springs Uplift, the Weber Sandstone has sufficient pore space to sequester 18 billion tons (Gt) of CO2, and the Madison Limestone has sufficient pore space to sequester 8 Gt of CO2. ?? 2011 Published by Elsevier Ltd.

Monitoring of leaked CO2 through sediment, water column and atmosphere in sub-seabed CCS experiment

NASA Astrophysics Data System (ADS)

Shitashima, K.; Sakamoto, A.; Maea, Y.

2013-12-01

CO2 capture and storage in sub-seabed geological formations (sub-seabed CCS) is currently being studied as a feasible option to mitigate the accumulation of anthropogenic CO2 in the atmosphere. In implementing sub-seabed CCS, detecting and monitoring the impact of the sequestered CO2 on the ocean environment is highly important. The first controlled CO2 release experiment, entitled 'Quantifying and Monitoring Potential Ecosystem Impacts of Geological Carbon Storage (QICS)', took place in Ardmucknish Bay, Oban, in May-July 2012. We applied the in-situ pH/pCO2/ORP sensor to the QICS experiment for detection and monitoring of leaked CO2, and carried out several observations. The on-line sensor that was connected by 400m of RS422 cable was deployed close to the CO2 leakage (bubbling) point, and the fluctuations of pH, pCO2 and ORP were monitored in real-time in a observation van on land. Three sets of off-line sensors were also placed on seafloor in respective points (release point, and two low impacted regions at 25m and 75m distant) for three months. The long-term monitoring of pH in sediment at 50cm depth under the seafloor was conducted. The spear type electrode was stabbed into sediment by diver near the CO2 leakage point. Wide-area mapping surveys of pH, pCO2 and ORP in seawater around the leakage point were carried out by AUV (REMUS-100) that some chemical sensors were installed in. The AUV cruised along the grid line in two layers of 4m and 2m above the seafloor during both of periods of low tide and high tide. Atmospheric CO2 in sea surface above the leakage point was observed by the LI-COR CO2 Analyzer. The analyzer was attached to the bow of ship, and the ship navigated a wide-area along a grid observation line during both of periods of low tide and high tide.

Breakup of last glacial deep stratification in the South Pacific

NASA Astrophysics Data System (ADS)

Basak, Chandranath; Fröllje, Henning; Lamy, Frank; Gersonde, Rainer; Benz, Verena; Anderson, Robert F.; Molina-Kescher, Mario; Pahnke, Katharina

2018-02-01

Stratification of the deep Southern Ocean during the Last Glacial Maximum is thought to have facilitated carbon storage and subsequent release during the deglaciation as stratification broke down, contributing to atmospheric CO2 rise. Here, we present neodymium isotope evidence from deep to abyssal waters in the South Pacific that confirms stratification of the deepwater column during the Last Glacial Maximum. The results indicate a glacial northward expansion of Ross Sea Bottom Water and a Southern Hemisphere climate trigger for the deglacial breakup of deep stratification. It highlights the important role of abyssal waters in sustaining a deep glacial carbon reservoir and Southern Hemisphere climate change as a prerequisite for the destabilization of the water column and hence the deglacial release of sequestered CO2 through upwelling.

How intensive agriculture affects surface-atmosphere exchange of nitrogen and carbon compounds over peatland

NASA Astrophysics Data System (ADS)

Bruemmer, C.; Richter, U.; Schrader, F.; Hurkuck, M.; Kutsch, W. L.

2016-12-01

Mid-latitude peatlands are often exposed to high atmospheric nitrogen deposition when located in close vicinity to agricultural land. As the impacts of altered deposition rates on nitrogen-limited ecosystems are poorly understood, we investigated the surface-atmosphere exchange of several nitrogen and carbon compounds using multiple high-resolution measurement techniques and modeling. Our study site was a protected semi-natural bog ecosystem. Local wind regime and land use in the adjacent area clearly regulated whether total reactive nitrogen (∑Nr) concentrations were ammonia (NH3) or NOx-dominated. Eddy-covariance measurements of NH3 and ∑Nr revealed concentration, temperature and surface wetness-dependent deposition rates. Intermittent periods of NH3 and ∑Nr emission likely attributed to surface water re-emission and soil efflux, respectively, were found, thereby indicating nitrogen oversaturation in this originally N-limited ecosystem. Annual dry plus wet deposition resulted in 20 to 25 kg N ha-1 depending on method and model used, which translated into a four- to fivefold exceedance of the ecosystem-specific critical load. As the bog site had likely been exposed to the observed atmospheric nitrogen burden over several decades, a shift in grass species' composition towards a higher number of nitrophilous plants was already visible. Three years of CO2 eddy flux measurements showed that the site was a small net sink in the range of 33 to 268 g CO2 m-2 yr-1. Methane emissions of 32 g CO2-eq were found to partly offset the sequestered carbon through CO2. Our study demonstrates the applicability of novel micrometeorological measurement techniques in biogeochemical sciences and stresses the importance of monitoring long-term changes in vulnerable ecosystems under anthropogenic pressure and climate change.

A guide to potential soil carbon sequestration; land-use management for mitigation of greenhouse gas emissions

USGS Publications Warehouse

Markewich, H.W.; Buell, G.R.

2001-01-01

Terrestrial carbon sequestration has a potential role in reducing the recent increase in atmospheric carbon dioxide (CO2) that is, in part, contributing to global warming. Because the most stable long-term surface reservoir for carbon is the soil, changes in agriculture and forestry can potentially reduce atmospheric CO2 through increased soil-carbon storage. If local governments and regional planning agencies are to effect changes in land-use management that could mitigate the impacts of increased greenhouse gas (GHG) emissions, it is essential to know how carbon is cycled and distributed on the landscape. Only then can a cost/benefit analysis be applied to carbon sequestration as a potential land-use management tool for mitigation of GHG emissions. For the past several years, the U.S. Geological Survey (USGS) has been researching the role of terrestrial carbon in the global carbon cycle. Data from these investigations now allow the USGS to begin to (1) 'map' carbon at national, regional, and local scales; (2) calculate present carbon storage at land surface; and (3) identify those areas having the greatest potential to sequester carbon.

Subtask 1.22 - Microbial Cycling of CH4, CO2, and N2O in a Wetlands Environment

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

Dingyi Ye; Bethany Kurz; Marc Kurz

Soil microbial metabolic activities play an important role in determining CO{sub 2}, CH{sub 4}, and N{sub 2}O fluxes from terrestrial ecosystems. To verify and evaluate CO{sub 2} sequestration potential by wetland restoration in the Prairie Pothole Region (PPR), as well as to address concern over restoration effects on CH{sub 4} and N{sub 2}O emissions, laboratory and in situ microcosm studies on microbial cycling of CO{sub 2}, CH{sub 4}, and N{sub 2}O were initiated. In addition, to evaluate the feasibility of the use of remote sensing to detect soil gas flux from wetlands, a remote-sensing investigation was also conducted. Results ofmore » the laboratory microcosm study unequivocally proved that restoration of PPR wetlands does sequester atmospheric CO{sub 2}. Under the experimental conditions, the simulated restored wetlands did not promote neither N{sub 2}O nor CH{sub 4} fluxes. Application of ammonia enhanced both N{sub 2}O and CH{sub 4} emission, indicating that restoration of PPR wetlands may reduce both N{sub 2}O and CH{sub 4} emission by cutting N-fertilizer input. Enhancement of CO{sub 2} emission by the N-fertilizer was observed, and this observation revealed an overlooked fact that application of N-fertilizer may potentially increase CO{sub 2} emission. In addition, the CO{sub 2} results also demonstrate that wetland restoration sequesters atmospheric carbon not only by turning soil conditions from aerobic to anoxic, but also by cutting N-fertilizer input that may enhance CO{sub 2} flux. The investigation on microbial community structure and population dynamics showed that under the experimental conditions restoration of the PPR wetlands would not dramatically increase population sizes of those microorganisms that produce N{sub 2}O and CH{sub 4}. Results of the in situ study proved that restoration of the PPR wetland significantly reduced CO{sub 2} flux. Ammonia enhanced the greenhouse gas emission and linearly correlated to the CO{sub 2} flux within the experimental rate range (46-200 kg N ha{sup -1}). The results also clarified that the overall reduction in global warming potential (GWP) by the PPR wetland restoration was mainly contributed from reduction in CO{sub 2} flux. These results demonstrate that restoration of currently farmed PPR wetlands will significantly reduce the overall GWP budget. Remote sensing investigations indicate that while the 15-meter resolution of the imagery was sufficient to delineate multiple zones in larger wetlands, it was not sufficient for correlation with the ground-based gas flux measurement data, which were collected primarily for smaller wetland sites (<250 meters) in the areas evaluated by this task. To better evaluate the feasibility of using satellite imagery to quantify wetland gas flux, either higher-resolution satellite imagery or gas flux data from larger wetland sites is needed.« less

Carbon sequestration associated to the land-use and land-cover changes in the forestry sector in Southern Brazil

NASA Astrophysics Data System (ADS)

Ronquim, Carlos C.; Silva, Ramon F. B.; de Figueiredo, Eduardo B.; Bordonal, Ricardo O.; de C. Teixeira, Antônio H.; Cochasrk, Thomas C. D.; Leivas, Janice F.

2016-10-01

We studied the Paraíba do Sul river watershed, São Paulo state (PSWSP), Southeastern Brazil, in order to assess the land use and cover (LULC) and their implications to the amount of carbon (C) stored in the forest cover between the years 1985 and 2015. The region covers an area of 1,395,975 ha. We used images made by the Operational Land Imager (OLI) sensor (OLI/Landsat-8) to produce mappings, and image segmentation techniques to produce vectors with homogeneous characteristics. The training samples and the samples used for classification and validation were collected from the segmented image. To quantify the C stocked in aboveground live biomass (AGLB), we used an indirect method and applied literature-based reference values. The recovery of 205,690 ha of a secondary Native Forest (NF) after 1985 sequestered 9.7 Tg (Teragram) of C. Considering the whole NF area (455,232 ha), the amount of C accumulated along the whole watershed was 35.5 Tg, and the whole Eucalyptus crop (EU) area (113,600 ha) sequestered 4.4 Tg of C. Thus, the total amount of C sequestered in the whole watershed (NF + EU) was 39.9 Tg of C or 145.6 Tg of CO2, and the NF areas were responsible for the largest C stock at the watershed (89%). Therefore, the increase of the NF cover contributes positively to the reduction of CO2 concentration in the atmosphere, and Reducing Emissions from Deforestation and Forest Degradation (REDD+) may become one of the most promising compensation mechanisms for the farmers who increased forest cover at their farms.

Ocean sequestration of crop residue carbon: recycling fossil fuel carbon back to deep sediments.

PubMed

Strand, Stuart E; Benford, Gregory

2009-02-15

For significant impact any method to remove CO2 from the atmosphere must process large amounts of carbon efficiently, be repeatable, sequester carbon for thousands of years, be practical, economical and be implemented soon. The only method that meets these criteria is removal of crop residues and burial in the deep ocean. We show here that this method is 92% efficient in sequestration of crop residue carbon while cellulosic ethanol production is only 32% and soil sequestration is about 14% efficient. Deep ocean sequestration can potentially capture 15% of the current global CO2 annual increase, returning that carbon backto deep sediments, confining the carbon for millennia, while using existing capital infrastructure and technology. Because of these clear advantages, we recommend enhanced research into permanent sequestration of crop residues in the deep ocean.

Native Soil Charcoal as a Model for Designing Biochar for Carbon Sequestration

EPA Science Inventory

Under changing climate a variety of mechanisms for removing carbon from the atmosphere and sequestering it elsewhere are being considered to reduce the forcing of the atmosphere. Amending soils with biochar has been proposed as one long-term means of sequestering carbon originat...

[Effects of land use change on carbon storage in terrestrial ecosystem].

PubMed

Yang, Jingcheng; Han, Xingguo; Huang, Jianhui; Pan, Qingmin

2003-08-01

Terrestrial ecosystem is an important carbon pool, which plays a crucial role in carbon biogeochemical cycle. Human activities such as fossil fuel combustion and land use change have resulted in carbon fluxes from terrestrial ecosystem to the atmosphere, which increased the atmospheric CO2 concentration, and reinforced the greenhouse effect. Land use change affects the structure and function of the terrestrial ecosystem, which causes its change of carbon storage. To a great extent, the change of carbon storage lies in the type of ecosystem and the change of land use patterns. The conversion of forest to agricultural land and pasture causes a large reduction of carbon storage in vegetation and soil, and the decrease of soil carbon concentration is mainly caused by the reduction of detritus, the acceleration of soil organic matter decomposition, and the destroy of physical protection to organic matter due to agricultural practices. The loss of soil organic matter appears at the early stage after deforestation, and the loss rate is influenced by many factors and soil physical, chemical and biological processes. The conversion of agricultural land and pasture to forest and many conservative agricultural practices can sequester atmospheric carbon in vegetation and soil. Vegetation can sequester large amounts of carbon from atmosphere, while carbon accumulation in soil varies greatly because of farming history and soil spatial heterogeneity. Conservative agricultural practices such as no-tillage, reasonable cropping system, and fertilization can influence soil physical and chemical characters, plant growth, quality and quantity of stubble, and soil microbial biomass and its activity, and hence, maintain and increase soil carbon concentration.

Biochar from Biomass and its Potential Agronomic and Environmental Use in Washington: A Promising Alternative to Drawdown Carbon from the Atmosphere and Develop a New Industry

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

Amonette, James E.; Garcia-Perez, Manuel; Sjoding, David

2016-03-04

Climate change is one of the most serious issues facing the world today. Increasing concentrations of carbon dioxide (CO 2) and other long-lived greenhouse gases (GHGs) in the atmosphere continue to warm the planet and destabilize the climate. It has been estimated that the impact from this warming could cost the state 10 billion per year by 2020, and 16 billion per year by 2040. Long-term solutions to the climate problem likely will require that large quantities of CO 2 be removed from the atmosphere. In fact, massive CO 2 drawdowns from the atmosphere have occurred in earth’s recent pastmore » from events occurring in our hemisphere. Studies of those analogs provide insight into the potential magnitude for specific actions to drawdown significant CO 2 from the atmosphere. One of these potential actions is the large-scale production of biochar from abundant woody biomass waste and its storage in soils, where it remains stable for hundreds to thousands of years. Moreover, for the carbon emission intensity of Washington’s fuel mix, biochar production from biomass is twice as effective in offsetting GHG emissions as complete biomass combustion of the same biomass. Washington State has large quantities of wood waste biomass that could be purposed for production of combined heat/power/biochar (CHPB) through existing biomass boilers. We propose to 1) evaluate the quantities of Washington wood waste biomass, 2) inventory existing boiler capacity and assess the technical merits and challenges to repurpose the boilers to CHPB, and 3) apply literature values and analog biochar examples to better quantify the extent of CO 2 drawdown that could be achieved in Washington State over the next century using engineered biochar. This white paper explores the potential to replicate the historical drawdowns of atmospheric CO 2, a topic the authors think should be part of current climate-change mitigation discussions. This document is a companion to a white paper titled Biochar from Wood Biomass and Agricultural Residues and its Potential Agronomic Use in Washington: A Tool to Improve Irrigation Water Use Efficiency, Energy Efficiency and Sequester Carbon (Amonette, et al., 2016, in preparation).« less

Improving farming practices reduces the carbon footprint of spring wheat production.

PubMed

Gan, Yantai; Liang, Chang; Chai, Qiang; Lemke, Reynald L; Campbell, Con A; Zentner, Robert P

2014-11-18

Wheat is one of the world's most favoured food sources, reaching millions of people on a daily basis. However, its production has climatic consequences. Fuel, inorganic fertilizers and pesticides used in wheat production emit greenhouse gases that can contribute negatively to climate change. It is unknown whether adopting alternative farming practices will increase crop yield while reducing carbon emissions. Here we quantify the carbon footprint of alternative wheat production systems suited to semiarid environments. We find that integrating improved farming practices (that is, fertilizing crops based on soil tests, reducing summerfallow frequencies and rotating cereals with grain legumes) lowers wheat carbon footprint effectively, averaging -256 kg CO2 eq ha(-1) per year. For each kg of wheat grain produced, a net 0.027-0.377 kg CO2 eq is sequestered into the soil. With the suite of improved farming practices, wheat takes up more CO2 from the atmosphere than is actually emitted during its production.

Improving farming practices reduces the carbon footprint of spring wheat production

NASA Astrophysics Data System (ADS)

Gan, Yantai; Liang, Chang; Chai, Qiang; Lemke, Reynald L.; Campbell, Con A.; Zentner, Robert P.

2014-11-01

Wheat is one of the world’s most favoured food sources, reaching millions of people on a daily basis. However, its production has climatic consequences. Fuel, inorganic fertilizers and pesticides used in wheat production emit greenhouse gases that can contribute negatively to climate change. It is unknown whether adopting alternative farming practices will increase crop yield while reducing carbon emissions. Here we quantify the carbon footprint of alternative wheat production systems suited to semiarid environments. We find that integrating improved farming practices (that is, fertilizing crops based on soil tests, reducing summerfallow frequencies and rotating cereals with grain legumes) lowers wheat carbon footprint effectively, averaging -256 kg CO2 eq ha-1 per year. For each kg of wheat grain produced, a net 0.027-0.377 kg CO2 eq is sequestered into the soil. With the suite of improved farming practices, wheat takes up more CO2 from the atmosphere than is actually emitted during its production.

Improving farming practices reduces the carbon footprint of spring wheat production

PubMed Central

Gan, Yantai; Liang, Chang; Chai, Qiang; Lemke, Reynald L.; Campbell, Con A.; Zentner, Robert P.

2014-01-01

Wheat is one of the world’s most favoured food sources, reaching millions of people on a daily basis. However, its production has climatic consequences. Fuel, inorganic fertilizers and pesticides used in wheat production emit greenhouse gases that can contribute negatively to climate change. It is unknown whether adopting alternative farming practices will increase crop yield while reducing carbon emissions. Here we quantify the carbon footprint of alternative wheat production systems suited to semiarid environments. We find that integrating improved farming practices (that is, fertilizing crops based on soil tests, reducing summerfallow frequencies and rotating cereals with grain legumes) lowers wheat carbon footprint effectively, averaging −256 kg CO2 eq ha−1 per year. For each kg of wheat grain produced, a net 0.027–0.377 kg CO2 eq is sequestered into the soil. With the suite of improved farming practices, wheat takes up more CO2 from the atmosphere than is actually emitted during its production. PMID:25405548

Serpentinite and the dawn of life

PubMed Central

Sleep, Norman H.; Bird, Dennis K.; Pope, Emily C.

2011-01-01

Submarine hydrothermal vents above serpentinite produce chemical potential gradients of aqueous and ionic hydrogen, thus providing a very attractive venue for the origin of life. This environment was most favourable before Earth's massive CO2 atmosphere was subducted into the mantle, which occurred tens to approximately 100 Myr after the moon-forming impact; thermophile to clement conditions persisted for several million years while atmospheric pCO2 dropped from approximately 25 bar to below 1 bar. The ocean was weakly acid (pH ∼ 6), and a large pH gradient existed for nascent life with pH 9–11 fluids venting from serpentinite on the seafloor. Total CO2 in water was significant so the vent environment was not carbon limited. Biologically important phosphate and Fe(II) were somewhat soluble during this period, which occurred well before the earliest record of preserved surface rocks approximately 3.8 billion years ago (Ga) when photosynthetic life teemed on the Earth and the oceanic pH was the modern value of approximately 8. Serpentinite existed by 3.9 Ga, but older rocks that might retain evidence of its presence have not been found. Earth's sequesters extensive evidence of Archaean and younger subducted biological material, but has yet to be exploited for the Hadean record. PMID:21930576

Sequestration of carbon dioxide and production of biomolecules using cyanobacteria.

PubMed

Upendar, Ganta; Singh, Sunita; Chakrabarty, Jitamanyu; Chandra Ghanta, Kartik; Dutta, Susmita; Dutta, Abhishek

2018-07-15

A cyanobacterial strain, Synechococcus sp. NIT18, has been applied to sequester CO 2 using sodium carbonate as inorganic carbon source due to its efficiency of CO 2 bioconversion and high biomass production. The biomass obtained is used for the extraction of biomolecules - protein, carbohydrate and lipid. The main objective of the study is to maximize the biomass and biomolecules production with CO 2 sequestration using cyanobacterial strain cultivated under different concentrations of CO 2 (5-20%), pH (7-11) and inoculum size (5-12.5%) within a statistical framework. Maximum sequestration of CO 2 and maximum productivities of protein, carbohydrate and lipid are 71.02%, 4.9 mg/L/day, 6.7 mg/L/day and 1.6 mg/L/day respectively, at initial CO 2 concentration: 10%, pH: 9 and inoculum size: 12.5%. Since flue gas contains 10-15% CO 2 and the present strain is able to sequester CO 2 in this range, the strain could be considered as a useful tool for CO 2 mitigation for greener world. Copyright © 2018 Elsevier Ltd. All rights reserved.

[Preliminary assessment of the potential of biochar technology in mitigating the greenhouse effect in China].

PubMed

Jiang, Zhi-Xiang; Zheng, Hao; Li, Feng-Min; Wang, Zhen-Yu

2013-06-01

The production of biochar by pyrolysis and its application to soil can sequester the CO2 which was absorbed by plants from atmosphere into soil, in addition it can also bring multiple benefits for agriculture production. On the basis of the available potential survey of the biomass residues from agriculture and forestry section, life cycle assessment was employed to quantify the potential of biochar technology in mitigation of greenhouse gases in our country. The results showed: In China, the amount of available biomass resource was 6.04 x 10(8) t every year and its net greenhouse effect potential was 5.32 x 10(8) t CO(2e) (CO(2e): CO2 equivalent), which was equivalent to 0.88 t CO(2e) for every ton biomass. The greatest of contributor to the total potential was plant carbon sequestration in soil as the form of biochar which accounts for 73.94%, followed by production of renewable energy and its percentage was 23.85%. In summary, production of biochar from agriculture and forestry biomass residues had a significant potential for our country to struggle with the pressure of greenhouse gas emission.

An Evaluation of Subsurface Microbial Activity Conditional to Subsurface Temperature, Porosity, and Permeability at North American Carbon Sequestration Sites

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

Wilson, B.; Mordensky, S.; Verba, Circe

Several nations, including the United States, recognize global climate change as a force transforming the global ecosphere. Carbon dioxide (CO 2) is a greenhouse gas that contributes to the evolving climate. Reduction of atmospheric CO 2 levels is a goal for many nations and carbon sequestration which traps CO 2 in the Earth’s subsurface is one method to reduce atmospheric CO 2 levels. Among the variables that must be considered in developing this technology to a national scale is microbial activity. Microbial activity or biomass can change rock permeability, alter artificial seals around boreholes, and play a key role inmore » biogeochemistry and accordingly may determine how CO 2 is sequestered underground. Certain physical parameters of a reservoir found in literature (e.g., temperature, porosity, and permeability) may indicate whether a reservoir can host microbial communities. In order to estimate which subsurface formations may host microbes, this report examines the subsurface temperature, porosity, and permeability of underground rock formations that have high potential to be targeted for CO 2 sequestration. Of the 268 North American wellbore locations from the National Carbon Sequestration Database (NATCARB; National Energy and Technology Laboratory, 2015) and 35 sites from Nelson and Kibler (2003), 96 sequestration sites contain temperature data. Of these 96 sites, 36 sites have temperatures that would be favorable for microbial survival, 48 sites have mixed conditions for supporting microbial populations, and 11 sites would appear to be unfavorable to support microbial populations. Future studies of microbe viability would benefit from a larger database with more formation parameters (e.g. mineralogy, structure, and groundwater chemistry), which would help to increase understanding of where CO 2 sequestration could be most efficiently implemented.« less

On nutrients and trace metals: Effects from Enhanced Weathering

NASA Astrophysics Data System (ADS)

Amann, T.; Hartmann, J.

2015-12-01

The application of rock flour on suitable land ("Enhanced Weathering") is one proposed strategy to reduce the increase of atmospheric CO2 concentrations. At the same time it is an old and established method to add fertiliser and influence soil properties. Investigations of this method focused on the impact on the carbonate system, as well as on engineering aspects of a large-scale application, but potential side effects were never discussed quantitatively. We analysed about 120,000 geochemically characterised volcanic rock samples from the literature. Applying basic statistics, theoretical release rates of nutrients and potential contaminants by Enhanced Weathering were evaluated for typical rock types. Applied rock material can contain significant amounts of essential or beneficial nutrients (potassium, phosphorus, micronutrients). Their release can partly cover the demand of major crops like wheat, rice or corn, thereby increasing crop yield on degraded soils. However, the concentrations of considered elements are variable within a specific rock type, depending on the geological setting. High heavy metal concentrations are found in (ultra-) basic rocks, the class with the highest CO2 drawdown potential. More acidic rocks contain less or no critical amounts, but sequester less CO2. Findings show that the rock selection determines the capability to supply significant amounts of nutrients, which could partly substitute industrial mineral fertiliser usage. At the same time, the release of harmful trace element has to be considered. Through careful selection of regionally available rocks, benefits could be maximised and drawbacks reduced. The deployment of Enhanced Weathering to sequester CO2 and to ameliorate soils necessitates an ecosystem management, considering the release and fate of weathered elements in plants, soils and water. Cropland with degraded soils would benefit while having a net negative CO2 effect, while other carbon dioxide removal strategies, like afforestation, biofuel production, and biochar application could benefit from Enhanced Weathering side effects, as organic carbon pools are positively influenced.

Elution of uranium and transition metals from amidoxime-based polymer adsorbents for sequestering uranium from seawater

DOE PAGES

Pan, Horng-Bin; Kuo, Li-Jung; Miyamoto, Naomi; ...

2015-11-30

High-surface-area amidoxime and carboxylic acid grafted polymer adsorbents developed at Oak Ridge National Laboratory were tested for sequestering uranium in a flowing seawater flume system at the PNNL-Marine Sciences Laboratory. FTIR spectra indicate that a KOH conditioning process is necessary to remove the proton from the carboxylic acid and make the sorbent effective for sequestering uranium from seawater. The alkaline conditioning process also converts the amidoxime groups to carboxylate groups in the adsorbent. Both Na 2CO 3 H 2O 2 and hydrochloric acid elution methods can remove ~95% of the uranium sequestered by the adsorbent after 42 days of exposuremore » in real seawater. The Na 2CO 3 H 2O 2 elution method is more selective for uranium than conventional acid elution. Iron and vanadium are the two major transition metals competing with uranium for adsorption to the amidoxime-based adsorbents in real seawater. Tiron (4,5-Dihydroxy-1,3-benzenedisulfonic acid disodium salt, 1 M) can remove iron from the adsorbent very effectively at pH around 7. The coordination between vanadium (V) and amidoxime is also discussed based on our 51V NMR data.« less

Sequestering CO2 in the Ocean: Options and Consequences

NASA Astrophysics Data System (ADS)

Rau, G. H.; Caldeira, K.

2002-12-01

The likelihood of negative climate and environmental impacts associated with increasing atmospheric CO2 has prompted serious consideration of various CO2 mitigation strategies. Among these are methods of capturing and storing of CO2 in the ocean. Two approaches that have received the most attention in this regard have been i) ocean fertilization to enhanced biological uptake and fixation of CO2, and ii) the chemical/mechanical capture and injection of CO2 into the deep ocean. Both methods seek to enhance or speed up natural mechanisms of CO2 uptake and storage by the ocean, namely i) the biological CO2 "pump" or ii) the passive diffusion of CO2 into the surface ocean and subsequent mixing into the deep sea. However, as will be reviewed, concerns about the capacity and effectiveness of either strategy in long-term CO2 sequestration have been raised. Both methods are not without potentially significant environmental impacts, and the costs of CO2 capture and injection (option ii) are currently prohibitive. An alternate method of ocean CO2 sequestration would be to react and hydrate CO2 rich waste gases (e.g., power plant flue gas) with seawater and to subsequently neutralize the resulting carbonic acid with limestone to produce calcium and bicarbonate ions in solution. This approach would simply speed up the CO2 uptake and sequestration that naturally (but very slowly) occurs via global carbonate weathering. This would avoid much of the increased acidity associated with direct CO2 injection while obviating the need for costly CO2 separation and capture. The addition of the resulting bicarbonate- and carbonate-rich solution to the ocean would help to counter the decrease in pH and carbonate ion concentration, and hence loss of biological calcification that is presently occurring as anthropogenic CO2 invades the ocean from the atmosphere. However, as with any approach to CO2 mitigation, the costs, impacts, risks, and benefits of this method need to be better understood and weighed against those of alternative strategies, including business as usual.

Evaluation of the sinks and sources of atmospheric CO2 by artificial upwelling.

PubMed

Pan, Yiwen; Fan, Wei; Huang, Ting-Hsuan; Wang, Shu-Lun; Chen, Chen-Tung Arthur

2015-04-01

Artificial upwelling is considered a promising way to reduce the accumulation of anthropogenic carbon dioxide in the atmosphere. This practice could transport nutrient-rich deep water to the euphotic zone, enhance phytoplankton growth and consequently increase organic carbon exportation to the deep ocean via the biological pump. However, only a few studies quantitatively assess changes in oceanic CO2 uptake resulting from artificial upwelling. This article uses a simulation to examine the effect of hypothetical artificial upwelling-induced variations of CO2 fugacity in seawater (fCO2) using observed carbon and nutrient data from 14 stations, ranging from 21 to 43°N, in the West Philippine Sea (WPS), the East China Sea (ECS) and the Sea of Japan. Calculations are based on two basic assumptions: First, a near-field mixing of a nutrient-rich deep-ocean water plume in a stratified ocean environment is assumed to form given the presence of an artificial upwelling devise with appropriate technical parameters. Second, it is assumed that photosynthesis of marine phytoplankton could deplete all available nutrients following the stoichiometry of the modified Redfield ratio C/H/O/N/S/P=103.1/181.7/93.4/11.7/2.1/1. Results suggest artificial upwelling has significant effects on regional changes in sea-air differences (ΔfCO2sea-air) and the carbon sequestration potential (ΔfCO2mixed-amb). Large variations of ΔfCO2sea-air and ΔfCO2mixed-amb are shown to be associated with different regions, seasons and technical parameters of the artificial upwelling device. With proper design, it is possible to reverse the contribution of artificial upwelling from a strong CO2 source to sink. Thus, artificial upwelling has the potential to succeed as a geoengineering technique to sequester anthropogenic CO2, with appropriate technical parameters in the right region and season. Copyright © 2014 Elsevier B.V. All rights reserved.

Carbon sequestration through urban ecosystem services: A case study from Finland.

PubMed

Kuittinen, Matti; Moinel, Caroline; Adalgeirsdottir, Kristjana

2016-09-01

Plants and soil are natural regulators of atmospheric CO2. Whereas plants sequester atmospheric carbon, soils deposit it for decades. As cities become increasingly more densely built, the available land area for such ecosystem services may decrease. We studied seven different housing areas in the Finnish city of Espoo to ascertain the extent to which site efficiency affects to the ecosystem services if the full life-cycle GHG emissions of these areas are taken into account. The results show that the impact of CO2 uptake through carbon sinks in growing plants and the uptake of soil organic carbon vary greatly. Its share of all emissions varied from a marginal value of 1.2% to a more considerable value of 11.9%. The highest potential was calculated for a detached house located on a large site, while the weakest was calculated for compact apartment blocks. The study revealed that in order to quantify this potential more accurately, several knowledge gaps must first be addressed. These include impartial growth algorithms for Nordic wood species, missing accumulation factors for soil organic carbon in cold climates and statistical maintenance scenarios for gardens. Copyright © 2016 Elsevier B.V. All rights reserved.

Breakup of last glacial deep stratification in the South Pacific.

PubMed

Basak, Chandranath; Fröllje, Henning; Lamy, Frank; Gersonde, Rainer; Benz, Verena; Anderson, Robert F; Molina-Kescher, Mario; Pahnke, Katharina

2018-02-23

Stratification of the deep Southern Ocean during the Last Glacial Maximum is thought to have facilitated carbon storage and subsequent release during the deglaciation as stratification broke down, contributing to atmospheric CO 2 rise. Here, we present neodymium isotope evidence from deep to abyssal waters in the South Pacific that confirms stratification of the deepwater column during the Last Glacial Maximum. The results indicate a glacial northward expansion of Ross Sea Bottom Water and a Southern Hemisphere climate trigger for the deglacial breakup of deep stratification. It highlights the important role of abyssal waters in sustaining a deep glacial carbon reservoir and Southern Hemisphere climate change as a prerequisite for the destabilization of the water column and hence the deglacial release of sequestered CO 2 through upwelling. Copyright © 2018 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works.

Carbon balance of South Asia constrained by passenger aircraft CO2 measurements

NASA Astrophysics Data System (ADS)

Patra, P. K.; Niwa, Y.; Schuck, T. J.; Brenninkmeijer, C. A.; Machida, T.; Matsueda, H.; Sawa, Y.

2011-12-01

Quantifying the fluxes of carbon dioxide (CO2) between the atmosphere and terrestrial ecosystems in all their diversity, across the continents, is important and urgent for implementing effective mitigating policies. Whereas much is known for Europe and North America for instance, in comparison, South Asia, with 1.6 billion inhabitants and considerable CO2 fluxes, remained terra incognita in this respect. The sole measurement site at Cape Rama does not constrain CO2 fluxes during the summer monsoon season. We use regional measurements of atmospheric CO2 aboard a Lufthansa passenger aircraft between Frankfurt (Germany) and Chennai (India) at cruise altitude, in addition to the existing network sites for 2008, to estimate monthly fluxes for 64-regions using Bayesian inversion and ACTM transport model simulations. The applicability of the model's transport parameterization is confirmed using multi-tracer (SF6, CH4, N2O) simulations for the CARIBIC datasets. The annual carbon flux obtained by including the aircraft data is twice as large as the fluxes simulated by a terrestrial ecosystem model that was applied to prescribe the fluxes used in the inversions. It is shown that South Asia sequestered carbon at a rate of 0.37±0.20 Pg C yr-1 for the years 2007 and 2008, primarily during the summer monsoon season when the water limitation for this tropical ecosystem is relaxed. The seasonality and the strength of the calculated monthly fluxes are successfully validated using independent measurements of vertical CO2 profiles over Delhi and spatial variations at cruising altitude by the CONTRAIL program over Asia aboard Japan Airlines passenger aircraft (Patra et al., 2011). Major challenges remain the verification of the inverse model flux seasonality and annual totals by bottom-up estimations using field measurements and terrestrial ecosystem models.

Assessment of policy impacts on carbon capture and sequestration and bioenergy for U.S.' coal and natural gas power plants

NASA Astrophysics Data System (ADS)

Spokas, K.; Patrizio, P.; Leduc, S.; Mesfun, S.; Kraxner, F.

2017-12-01

Reducing electricity-sector emissions relies heavily on countries' abilities to either transition away from carbon-intensive energy generation or to sequester its resultant emissions with carbon capture and storage (CCS) technologies. The use of biomass energy technologies in conjunction with carbon capture and sequestration (BECCS) presents the opportunity for net reductions in atmospheric carbon dioxide. In this study, we investigate the limitations of several common policy mechanisms to incentivize the deployment of BECCS using the techno-economic spatial optimization model BeWhere (www.iiasa.ac.at/bewhere). We consider a set of coal and natural gas power plants in the United States (U.S.) selected using a screening process that considers capacity, boiler age, and capacity factor for electricity-generation units from the EPA 2014 eGRID database. The set makes up 470 GW of generation, and produces 8,400 PJ and 2.07 GtCO2 annually. Co-firing up to 15% for coal power plants is considered, using woody-biomass residues sourced from certified and managed U.S. forests obtained from the G4M (www.iiasa.ac.at/g4m) and GeoWiki (www.geo-wiki.org) database. Geologic storage is considered with injectivity and geomechanical limitations to ensure safe storage. Costs are minimized under two policy mechanisms: a carbon tax and geologic carbon sequestration credits, such as the Q45 credits. Results show that the carbon tax scenario incentivizes co-firing at low to medium carbon taxes, but is replaced by CCS at higher tax values. Carbon taxes do not strongly incentivize BECCS, as negative emissions associated with sequestering carbon content are not accounted as revenue. On the other hand, carbon credit scenarios result in significant CCS deployment, but lack any incentive for co-firing.

Does high reactive nitrogen input from the atmosphere decrease the carbon sink strength of a peatland?

NASA Astrophysics Data System (ADS)

Brümmer, Christian; Zöll, Undine; Hurkuck, Miriam; Schrader, Frederik; Kutsch, Werner

2017-04-01

Mid-latitude peatlands are often exposed to high atmospheric nitrogen deposition when located in close vicinity to agricultural land. As the impacts of altered deposition rates on nitrogen-limited ecosystems are poorly understood, we investigated the surface-atmosphere exchange of several nitrogen and carbon compounds using multiple high-resolution measurement techniques and modeling. Our study site was a protected semi-natural bog ecosystem. Local wind regime and land use in the adjacent area clearly regulated whether total reactive nitrogen (ΣNr) concentrations were ammonia (NH3) or NOx-dominated. Eddy-covariance measurements of NH3 and ΣNr revealed concentration, temperature and surface wetness-dependent deposition rates. Intermittent periods of NH3 and ΣNr emission likely attributed to surface water re-emission and soil efflux, respectively, were found, thereby indicating nitrogen oversaturation in this originally N-limited ecosystem. Annual dry plus wet deposition resulted in 20 to 25 kg N ha-1 depending on method and model used, which translated into a four- to fivefold exceedance of the ecosystem-specific critical load. As the bog site had likely been exposed to the observed atmospheric nitrogen burden over several decades, a shift in grass species' composition towards a higher number of nitrophilous plants was already visible. Three years of CO2 eddy flux measurements showed that the site was a small net sink in the range of 33 to 268 g CO2 m-2 yr-1. Methane emissions of 32 g CO2-eq were found to partly offset the sequestered carbon through CO2. Our study indicates that the sink strength of the peatland has likely been decreased through elevated N deposition over the past decades. It also demonstrates the applicability of novel micrometeorological measurement techniques in biogeochemical sciences and stresses the importance of monitoring long-term changes in vulnerable ecosystems under anthropogenic pressure and climate change.

Current and Projected Carbon Dynamics in US Agricultural Systems

NASA Astrophysics Data System (ADS)

Ogle, S. M.; Paustian, K.; Zhang, Y.; Kent, J.; Gurung, R.; Klotz, R.

2016-12-01

Agricultural lands occur across a variety of landscapes in the United States, and carbon dynamics are largely controlled by management decisions along with edaphic characteristics, climate and other environmental drivers. Due to the influence of management, there is potential to sequester carbon in soils with adoption of conservation practices, such as setting aside degraded land from production, limiting tillage disturbance, enhancing crop production with higher yielding varieties, planting cover crops, and restoring wetlands where they have been drained for crop production. In 2010, the level of sequestration in mineral soils across US croplands was 48 million metric tonnes CO2 equivalent, which is down from the high during the past 25 years of 90 million metric tonnes CO2 equivalent. In contrast, drained wetlands that are used for crop production were emitting 22.1 million metric tonnes CO2 equivalent in 2010. In the short term, restoring drained wetlands would decrease CO2emissions to the atmosphere, and even with the additional CH4 emissions from restored wetlands, there would an overall reduction in greenhouse gas emissions from these lands. In turn, this would make a significant contribution to the USDA Climate Smart Agriculture Plan for reducing greenhouse gas emissions by 120 million metric tonnes CO2 equivalent in support of the Paris Agreement. The potential to sequester carbon in the future will also be impacted by climate change, in addition to the management decisions of land managers. We simulated future carbon dynamics through 2060 based on climate change projections for RCP 2.5, 4.5 and 8.5 scenarios, with and without CO2 fertilization effects. We are using the results as input to a general equilibrium model for the agricultural economic sector to better understand the economic consequences of climate change and the potential for greenhouse gas mitigation. By evaluating the influence of climate change and economic welfare, our study is providing a basis to understand the potential long-term contribution of carbon sequestration in support of a Climate Smart Agriculture Program in the United States.

Agricultural peatland restoration: effects of land-use change on greenhouse gas (CO2 and CH4) fluxes in the Sacramento-San Joaquin Delta.

PubMed

Knox, Sara Helen; Sturtevant, Cove; Matthes, Jaclyn Hatala; Koteen, Laurie; Verfaillie, Joseph; Baldocchi, Dennis

2015-02-01

Agricultural drainage of organic soils has resulted in vast soil subsidence and contributed to increased atmospheric carbon dioxide (CO2) concentrations. The Sacramento-San Joaquin Delta in California was drained over a century ago for agriculture and human settlement and has since experienced subsidence rates that are among the highest in the world. It is recognized that drained agriculture in the Delta is unsustainable in the long-term, and to help reverse subsidence and capture carbon (C) there is an interest in restoring drained agricultural land-use types to flooded conditions. However, flooding may increase methane (CH4) emissions. We conducted a full year of simultaneous eddy covariance measurements at two conventional drained agricultural peatlands (a pasture and a corn field) and three flooded land-use types (a rice paddy and two restored wetlands) to assess the impact of drained to flooded land-use change on CO2 and CH4 fluxes in the Delta. We found that the drained sites were net C and greenhouse gas (GHG) sources, releasing up to 341 g C m(-2) yr(-1) as CO2 and 11.4 g C m(-2) yr(-1) as CH4. Conversely, the restored wetlands were net sinks of atmospheric CO2, sequestering up to 397 g C m(-2) yr(-1). However, they were large sources of CH4, with emissions ranging from 39 to 53 g C m(-2) yr(-1). In terms of the full GHG budget, the restored wetlands could be either GHG sources or sinks. Although the rice paddy was a small atmospheric CO2 sink, when considering harvest and CH4 emissions, it acted as both a C and GHG source. Annual photosynthesis was similar between sites, but flooding at the restored sites inhibited ecosystem respiration, making them net CO2 sinks. This study suggests that converting drained agricultural peat soils to flooded land-use types can help reduce or reverse soil subsidence and reduce GHG emissions. © 2014 John Wiley & Sons Ltd.

Historical Carbon Dioxide Emissions Caused by Land-Use Changes are Possibly Larger than Assumed

NASA Technical Reports Server (NTRS)

Arneth, A.; Sitch, S.; Pongratz, J.; Stocker, B. D.; Ciais, P.; Poulter, B.; Bayer, A. D.; Bondeau, A.; Calle, L.; Chini, L. P.;

Defining the `negative emission' capacity of global agriculture deployed for enhanced rock weathering

NASA Astrophysics Data System (ADS)

Beerling, D. J.; Taylor, L.; Banwart, S. A.; Kantzas, E. P.; Lomas, M.; Mueller, C.; Ridgwell, A.; Quegan, S.

2016-12-01

Enhanced rock weathering involves application of crushed silicates (e.g. basalt) to the landscape to accelerate their chemical breakdown to release base cations and form bicarbonate that ultimate sequester CO2 in the oceans. Global croplands cover an area of 12 million km2 and might be deployed for long-term removal of anthropogenic CO2 through enhanced rock weathering with a number of co-benefits for food security. This presentation assesses the potential of this strategy to contribute to `negative emissions' as defined by a suite of simulations coupling a detailed model of rock grain weathering by crop root-microbial processes with a managed land dynamic global vegetation model driven by the `business as usual' future climate change scenarios. We calculate potential atmospheric CO2 drawdown over the next century by introducing a strengthened C-sink term into the global carbon cycle model within an intermediate complexity Earth system model. Our simulations indicate agricultural lands deployed in this way constitute a `low tech' biological negative emissions strategy. As part of a wider portfolio of options, this strategy might contribute to limiting future warming to 2oC, subject to economic costs and energy requirements.

Coupled thermal–hydrological–mechanical modeling of CO 2 -enhanced coalbed methane recovery

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

Ma, Tianran; Rutqvist, Jonny; Oldenburg, Curtis M.

CO 2 -enhanced coalbed methane recovery, also known as CO 2 -ECBM, is a potential win-win approach for enhanced methane production while simultaneously sequestering injected anthropogenic CO 2 to decrease CO 2 emissions into the atmosphere. Here, CO 2 -ECBM is simulated using a coupled thermal–hydrological–mechanical (THM) numerical model that considers multiphase (gas and water) flow and solubility, multicomponent (CO 2 and CH 4 ) diffusion and adsorption, heat transfer and coal deformation. The coupled model is based on the TOUGH-FLAC simulator, which is applied here for the first time to model CO 2 -ECBM. The capacity of the simulatormore » for modeling methane production is verified by a code-to-code comparison with the general-purpose finite-element solver COMSOL. Then, the TOUGH-FLAC simulator is applied in an isothermal simulation to study the variations in permeability evolution during a CO 2 -ECBM operation while considering four different stress-dependent permeability models that have been implemented into the simulator. Finally, the TOUGH-FLAC simulator is applied in non-isothermal simulations to model THM responses during a CO 2 -ECBM operation.Our simulations show that the permeability evolution, mechanical stress, and deformation are all affected by changes in pressure, temperature and adsorption swelling, with adsorption swelling having the largest effect. The calculated stress changes do not induce any mechanical failure in the coal seam, except near the injection well in one case of a very unfavorable stress field.« less

Coupled thermal–hydrological–mechanical modeling of CO 2 -enhanced coalbed methane recovery

DOE PAGES

Ma, Tianran; Rutqvist, Jonny; Oldenburg, Curtis M.; ...

2017-05-22

CO 2 -enhanced coalbed methane recovery, also known as CO 2 -ECBM, is a potential win-win approach for enhanced methane production while simultaneously sequestering injected anthropogenic CO 2 to decrease CO 2 emissions into the atmosphere. Here, CO 2 -ECBM is simulated using a coupled thermal–hydrological–mechanical (THM) numerical model that considers multiphase (gas and water) flow and solubility, multicomponent (CO 2 and CH 4 ) diffusion and adsorption, heat transfer and coal deformation. The coupled model is based on the TOUGH-FLAC simulator, which is applied here for the first time to model CO 2 -ECBM. The capacity of the simulatormore » for modeling methane production is verified by a code-to-code comparison with the general-purpose finite-element solver COMSOL. Then, the TOUGH-FLAC simulator is applied in an isothermal simulation to study the variations in permeability evolution during a CO 2 -ECBM operation while considering four different stress-dependent permeability models that have been implemented into the simulator. Finally, the TOUGH-FLAC simulator is applied in non-isothermal simulations to model THM responses during a CO 2 -ECBM operation.Our simulations show that the permeability evolution, mechanical stress, and deformation are all affected by changes in pressure, temperature and adsorption swelling, with adsorption swelling having the largest effect. The calculated stress changes do not induce any mechanical failure in the coal seam, except near the injection well in one case of a very unfavorable stress field.« less

Terrestrial aftermath of the Moon-forming impact.

PubMed

Sleep, Norman H; Zahnle, Kevin J; Lupu, Roxana E

2014-09-13

Much of the Earth's mantle was melted in the Moon-forming impact. Gases that were not partially soluble in the melt, such as water and CO2, formed a thick, deep atmosphere surrounding the post-impact Earth. This atmosphere was opaque to thermal radiation, allowing heat to escape to space only at the runaway greenhouse threshold of approximately 100 W m(-2). The duration of this runaway greenhouse stage was limited to approximately 10 Myr by the internal energy and tidal heating, ending with a partially crystalline uppermost mantle and a solid deep mantle. At this point, the crust was able to cool efficiently and solidified at the surface. After the condensation of the water ocean, approximately 100 bar of CO2 remained in the atmosphere, creating a solar-heated greenhouse, while the surface cooled to approximately 500 K. Almost all this CO2 had to be sequestered by subduction into the mantle by 3.8 Ga, when the geological record indicates the presence of life and hence a habitable environment. The deep CO2 sequestration into the mantle could be explained by a rapid subduction of the old oceanic crust, such that the top of the crust would remain cold and retain its CO2. Kinematically, these episodes would be required to have both fast subduction (and hence seafloor spreading) and old crust. Hadean oceanic crust that formed from hot mantle would have been thicker than modern crust, and therefore only old crust underlain by cool mantle lithosphere could subduct. Once subduction started, the basaltic crust would turn into dense eclogite, increasing the rate of subduction. The rapid subduction would stop when the young partially frozen crust from the rapidly spreading ridge entered the subduction zone. © 2014 The Author(s) Published by the Royal Society. All rights reserved.

Assessment of carbon sequestration potential of revegetated coal mine overburden dumps: A chronosequence study from dry tropical climate.

PubMed

Ahirwal, Jitendra; Maiti, Subodh Kumar

2017-10-01

Development of secondary forest as post-mining land use in the surface coal mining degraded sites is of high research interest due to its potential to sequester atmospheric carbon (C). The objectives of this study were to assess the improvement in mine soil quality and C sequestration potential of the post-mining reclaimed land with time. Hence, this study was conducted in reclaimed chronosequence sites (young, intermediate and old) of a large open cast coal project (Central Coal Fields Limited, Jharkhand, India) and results were compared to a reference forest site (Sal forest, Shorea robusta). Mine soil quality was assessed in terms of accretion of soil organic carbon (SOC), available nitrogen (N) and soil CO 2 flux along with the age of revegetation. After 14 years of revegetation, SOC and N concentrations increased three and five-fold, respectively and found equivalent to the reference site. Accretion of SOC stock was estimated to be 1.9 Mg C ha -1 year -1 . Total ecosystem C sequestered after 2-14 years of revegetation increased from 8 Mg C ha -1 to 90 Mg C ha -1 (30-333 Mg CO 2 ha -1 ) with an average rate of 6.4 Mg C ha -1 year -1 . Above ground biomass contributes maximum C sequestrate (50%) in revegetated site. CO 2 flux increased with age of revegetation and found 11, 33 and 42 Mg CO 2 ha -1 year -1 in younger, intermediate and older dumps, respectively. Soil respiration in revegetated site is more influenced by the temperature than soil moisture. Results of the study also showed that trees like, Dalbergia sissoo and Heterophragma adenophyllum should be preferred for revegetation of mine degraded sites. Copyright © 2017 Elsevier Ltd. All rights reserved.

Climate Change Mitigation through Enhanced Weathering in Bioenergy Crops

NASA Astrophysics Data System (ADS)

Kantola, I. B.; Masters, M. D.; Wolz, K. J.; DeLucia, E. H.

2016-12-01

Bioenergy crops are a renewable alternative to fossil fuels that reduce the net flux of CO2 to the atmosphere through carbon sequestration in plant tissues and soil. A portion of the remaining atmospheric CO2 is naturally mitigated by the chemical weathering of silica minerals, which sequester carbon as carbonates. The process of mineral weathering can be enhanced by crushing the minerals to increase surface area and applying them to agricultural soils, where warm temperatures, moisture, and plant roots and root exudates accelerate the weathering process. The carbonate byproducts of enhanced weathering are expected accumulate in soil water and reduce soil acidity, reduce nitrogen loss as N2O, and increase availability of certain soil nutrients. To determine the potential of enhanced weathering to alter the greenhouse gas balance in both annual (high disturbance, high fertilizer) and perennial (low disturbance, low fertilizer) bioenergy crops, finely ground basalt was applied to fields of maize, soybeans, and miscanthus at the University of Illinois Energy Farm. All plots showed an immediate soil temperature response at 10 cm depth, with increases of 1- 4 °C at midday. Early season CO2 and N2O fluxes mirrored soil temperature prior to canopy closure in all crops, while total N2O fluxes from miscanthus were lower than corn and soybeans in both basalt treatment and control plots. Mid-season N2O production was reduced in basalt-treated corn compared to controls. Given the increasing footprint of bioenergy crops, the ability to reduce GHG emissions in basalt-treated fields has the potential to mitigate atmospheric warming while benefitting soil fertility with the byproducts of weathering.

Soil Organic Carbon Sequestration by Tillage and Crop Rotation: A Global Data Analysis

DOE Data Explorer

West, Tristram O. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Post, Wilfred M. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States)

2002-01-01

Changes in agricultural management can potentially increase the accumulation rate of soil organic carbon (SOC), thereby sequestering CO2 from the atmosphere. This study was conducted to quantify potential soil carbon (C) sequestration rates for different crops in response to decreasing tillage intensity or enhancing rotation complexity, and to estimate the duration of time over which sequestration may occur. Analyses of C sequestration rates were completed using a global database of 67 long-term agricultural experiments, consisting of 276 paired treatments. Results indicate, on average, that a change from conventional tillage (CT) to no-till (NT) can sequester 57 ± 14 g C m^–2 yr^–1, excluding wheat (Triticum aestivum L.)-fallow systems which may not result in SOC accumulation with a change from CT to NT. Enhancing rotation complexity can sequester an average 14 ± 11 g C m^–2 yr^–1, excluding a change from continuous corn (Zea mays L.) to corn-soybean (Glycine max L.) which may not result in a significant accumulation of SOC. Carbon sequestration rates, with a change from CT to NT, can be expected to peak in 5-10 yr with SOC reaching a new equilibrium in 15-20 yr. Following initiation of an enhancement in rotation complexity, SOC may reach a new equilibrium in approximately 40-60 yr. Carbon sequestration rates, estimated for a number of individual crops and crop rotations in this study, can be used in spatial modeling analyses to more accurately predict regional, national, and global C sequestration potentials.

Net ecosystem exchange of CO2 and CH4 in the high arctic (81°N) during the growing season

NASA Astrophysics Data System (ADS)

Barker, J. D.; St. Louis, V. L.; Graydon, J. A.; Lehnherr, I.

2009-12-01

The role of high arctic ecosystems in the global carbon budget has attracted scientific interest because a) arctic terrestrial ecosystems currently store significant amounts of organic carbon in permafrost and poorly drained tundra soils, and b) the arctic climate system is changing rapidly in response to global warming. The role of the high arctic terrestrial ecosystem as either a source or sink of atmospheric CO2 is unknown, although it is generally assumed that it will become a source of CO2 to the atmosphere as climate change continues to warm the region and previously sequestered organic matter in soils is mineralized as the active layer develops. We will present data on the net ecosystem exchange (NEE) of CO2 from high arctic tundra near Lake Hazen, Quittinirpaaq National Park (81°N) during the 2008 and 2009 growing seasons, collected using an eddy covariance flux tower. This is the first report of NEE from such a northerly latitude. We will also present data on the exchange of CH4 with tundra soils collected using static chambers. The tundra at Lake Hazen was a continuous CO2 sink during the growing season, and is carbon neutral during snow cover conditions in early spring. The CO2 flux correlated strongly with PAR and soil temperature. Despite active layer development at the site during our observation period (11 cm in 2008, 37 cm in 2009), no evidence of a corresponding CO2 pulse to the atmosphere was detected. Soil respiration rates, separately measured using a LiCOR 6400, indicated a correlation between soil respiration and plant cover corresponded. The strong correlation between NEE and vegetation parameters suggests that as vegetation cover increases in the high arctic in response to climate warming, the tundra at Lake Hazen may continue to function as a carbon sink despite continued active layer development. Dry tundra soils always consumed CH4 at our site, suggesting that parts of the high Arctic are actually sinks for this strong greenhouse gas.

Long-Term Trends in the Global Carbon Cycle: Biogeochemical Records of the Past 205 myrs

NASA Astrophysics Data System (ADS)

Katz, M. E.; Fennel, K.; Berner, R. A.; Falkowski, P. G.

2005-12-01

Atmospheric and seawater chemistry are modified through time by both geological and biological processes: tectonic outgassing in combination with erosional processes are the primary suppliers of most major elements in geochemical cycles; biologically-mediated redox processes alter mobile elemental reservoirs before geologic processes sequester (remove) elements from these mobile reservoirs. We present Jurassic-Cenozoic carbon isotope records for carbonates and organic matter generated from bulk sediment samples from the Atlantic (sample resolution of 200 kyrs), and infer from these records changes in redox conditions and biological processes that affected atmospheric and seawater chemistry through time. We use our carbon isotope records with published sulfur isotopes of sulfates in model simulations to reconstruct carbon burial, pCO2 and pO2 over the past 205 myrs; our model results indicate that organic C burial and pO2 have increased, while pCO2 has decreased. The evolution and expansion of the larger-celled eucaryotic phytoplankton of the red-plastid lineage, coupled with the opening of the Atlantic Ocean basin and global sea-level rise, led to this increase in organic carbon burial beginning in the Early Jurassic as the supercontinent Pangea broke apart. This organic C burial increased the oxidation state of Earth's surface reservoirs while drawing down atmospheric CO2, which in turn acted as a strong selective agent in both marine and terrestrial primary producers, resulting in the rise in C4 and beta-carboxylation photosynthetic pathways in the latter part of the Cenozoic. At the same time, O2 levels approximately doubled, with relatively fast increases in the Early Jurassic and the Eocene. The rise of oxygen may have been a key factor in the evolution, radiation, and subsequent increase in the average size of placental mammals during the Cenozoic.

A Policy Option To Provide Sufficient Funding For Massive-Scale Sequestration of CO2

NASA Astrophysics Data System (ADS)

Kithil, P. W.

2007-12-01

Global emissions of CO2 now are nearly 30 billion tons per year, and are growing rapidly due to strong economic growth. Atmospheric levels of CO2 have reached 380 ppm and recent reports suggest the rate of increase has gone from 1% per year in the 1990's to 3% per year now - with potential to cross 550ppm in the 2020 decade. Without stabilization of atmospheric CO2 below 550ppm, climate models predict unacceptably higher average temperatures with significant risk of runaway global warming this century. While there is much talk about reducing CO2 emissions by switching to non-fossil energy sources, imposing energy efficiency, and a host of other changes, there are no new large-scale energy sources on the horizon. The options are to impose draconian cuts in fossil energy consumption that will keep us below 550ppm (devastating the global economy) - or to adopt massive-scale sequestration of CO2. Three approaches are feasible: biological ocean sequestration, geologic sequestration, and biological terrestrial sequestration. Biological sequestration is applicable to all CO2 sources, whereas geologic sequestration is limited to fossil-fuel power plants and some large point-source emitters such as cement plants and large industrial facilities. Sequestration provides a direct mechanism for reducing atmospheric levels of CO2, whereas offsetting technologies such as wind power or improved efficiency, reduce the need for more fossil fuels but do not physically remove CO2 from the environment. The primary geologic technique, carbon capture & sequestration (CCS), prevents CO2 from entering the atmosphere but likewise does not reduce existing levels of atmospheric CO2. Biological sequestration (ocean or terrestrial) physically removes CO2 from the atmosphere. Since we cannot shut down our global economy, urgent action is needed to counteract CO2 emissions, and avoid catastrophic climate change. Given the long lead time and/or small impact of offsetting energy sources, sequestration is the only way to achieve near and medium-term reductions in atmospheric CO2 levels. To finance massive-scale sequestration of CO2, we propose the World Trade Organization (WTO) become an active player in the sequestration market. Given the WTO's role as overseer of international trade agreements annually representing 30 trillion in imports and exports of goods and services, it is by far the largest global economic force and therefore offers the broadest economic base. Absent a real solution to CO2 emissions, the global economy - and world trade - will shrink dramatically. The WTO can jumpstart the market for CO2 sequestration by issuing long term contracts to purchase bona fide sequestration-derived CO2 credits. Under this proposal, an initial price of 100 per ton which steps-down by 5% per year could bring forth the sequestration investment needed to achieve upwards of 10 billion tons sequestered CO2 per year by 2025 (seven billion tons from biological ocean sequestration and at least three billion tons from geologic and terrestrial sequestration). Assuming a contract term of 40 years, and a parallel commodity market continues to develop for CO2 credits, at some time in the future the WTO's contractual price will be less than the commodity market price - and the WTO begins to recover its investment. Under one set of assumptions, the net WTO annual subsidy would peak at $86 billion by 2022, equal to an across-the-board WTO tariff on imports and exports of about 1.01%, then become positive a few years later as the market price climbed above WTO's contracted price. Under this proposal, the WTO effectively subsidizes CO2 sequestration in the near to medium term and then recoups its investment and reaps large profits over the long term.

Global Sequestration Potential of Increased Organic Carbon in Cropland Soils.

PubMed

Zomer, Robert J; Bossio, Deborah A; Sommer, Rolf; Verchot, Louis V

2017-11-14

The role of soil organic carbon in global carbon cycles is receiving increasing attention both as a potentially large and uncertain source of CO 2 emissions in response to predicted global temperature rises, and as a natural sink for carbon able to reduce atmospheric CO 2 . There is general agreement that the technical potential for sequestration of carbon in soil is significant, and some consensus on the magnitude of that potential. Croplands worldwide could sequester between 0.90 and 1.85 Pg C/yr, i.e. 26-53% of the target of the "4p1000 Initiative: Soils for Food Security and Climate". The importance of intensively cultivated regions such as North America, Europe, India and intensively cultivated areas in Africa, such as Ethiopia, is highlighted. Soil carbon sequestration and the conservation of existing soil carbon stocks, given its multiple benefits including improved food production, is an important mitigation pathway to achieve the less than 2 °C global target of the Paris Climate Agreement.

The Anthropogenic Era Began Thousands of Years Ago

NASA Astrophysics Data System (ADS)

Ruddiman, W. F.

2003-12-01

The anthropogenic era is generally thought to have begun about 150 years ago when the industrial revolution began producing CO2 and CH4 at rates sufficient to alter atmospheric compositions. The hypothesis proposed here is that anthropogenic emissions first altered atmospheric gas concentrations (and climate) thousands of years ago. This hypothesis rests on three arguments: (1) Cyclic variations in CO2 and CH4 driven by Earth-orbital changes during the last 400,000 years predict decreases of both gases throughout the Holocene, but CO2 began an anomalous increase near 8000 years ago and CH4 about 5000 years ago. (2) Published explanations attributing these Holocene gas increases to natural forcing can be rejected based on available paleoclimatic evidence. (3) Archeological, cultural, historical, and geologic sources provide viable explanations tied to anthropogenic changes that emerged from early agriculture in Eurasia, including forest clearance after 8000 years ago and lowland irrigation for rice farming by 5000 years ago. Prior to the industrial era, these emissions caused a mean-annual warming effect of ~0.8oC globally and 1.5-2oC at high latitudes. The early-anthropogenic warming counteracted most of a natural cooling that would otherwise have occurred, and it may have prevented a glaciation in northeastern Canada predicted by two kinds of climatic models. CO2 decreases as large as 10 ppm during the last 1000 years cannot be explained by solar-volcanic forcing without violating constraints imposed by reconstructions of northern hemisphere temperature. The CO2 decreases can be explained by bubonic plague pandemics that the caused widespread abandonment of western Eurasian farms documented in historical records. Rapid regrowth of forests on millions of abandoned farms could have sequestered enough carbon to explain the observed CO2 decreases. Plague-driven CO2 decreases were a significant causal factor in the cooler temperatures of the Little Ice Age from 1300 to 1900 A.D.

Partitioning of ocean and land uptake of CO2 as inferred by delta C-13 measurements from the NOAA Climate Monitoring and Diagnostics Laboratory Global Air Sampling Network

NASA Technical Reports Server (NTRS)

Ciais, Philippe; Tans, Pieter P.; White, James W. C.; Trolier, Michael; Francey, Roger J.; Berry, Joe A.; Randall, David R.; Sellers, Piers J.; Collatz, James G.; Schimel, David S.

1995-01-01

Using delta C-13 measurements in atmospheric CO2 from a cooperative global air sampling network, we determined the partitioning of the net uptake of CO2 between ocean and land as a function of latitude and time. The majority of delta C-13 measurements were made at the Institute of Arctic and Alpine Research (INSTAAR) of the University of Colorado. We perform an inverse deconvolution of both CO2 and delta C-13 observations, using a two-dimensional model of atmospheric transport. Also, the discrimination against C-13 by plant photosynthesis, as a function of latitude and time, is calculated from global runs of the simple biosphere (SiB) model. Uncertainty due to the longitudinal structure of the data, which is not represented by the model, is studied through a bootstrap analysis by adding and omitting measurement sites. The resulting error estimates for our inferred sources and sinks are of the order of 1 GTC (1 GTC = 10(exp 15) gC). Such error bars do not reflect potential systematic errors arising from our estimates of the isotopic disequilibria between the atmosphere and the oceans and biosphere, which are estimated in a separate sensitivity analysis. With respect to global totals for 1992 we found that 3.2 GTC of carbon dissolved into the ocean and that 1.5 GTC were sequestered by land ecosystems. Northern hemisphere ocean gyres north of 15 deg N absorbed 2.7 GTC. The equatorial oceans between 10 deg S and 10 deg N were a net source to the atmosphere of 0.9 GTC. We obtained a sink of 1.6 GTC in southern ocean gyres south of 20 deg S, although the deconvolution is poorly constrained by sparse data coverage at high southern latitudes. The seasonal uptake of CO2 in the northern gyres appears to be correlated with a bloom of phytoplankton in surface waters. On land, northern temperate and boreal ecosystems between 35 deg N and 65 deg N were found to be a major sink of CO2 in 1992, as large as 3.5 GTC. Northern tropical ecosystems (equator-30 deg N) appear to be a net source to the source to the atmosphere of 2 GTC which could reflect biomass burning. A small sink, 0.3 GTC, was inferred for southern tropical ecosystems (30 deg S-equator).

Modeling syngas-fired gas turbine engines with two dilutants

NASA Astrophysics Data System (ADS)

Hawk, Mitchell E.

2011-12-01

Prior gas turbine engine modeling work at the University of Wyoming studied cycle performance and turbine design with air and CO2-diluted GTE cycles fired with methane and syngas fuels. Two of the cycles examined were unconventional and innovative. The work presented herein reexamines prior results and expands the modeling by including the impacts of turbine cooling and CO2 sequestration on GTE cycle performance. The simple, conventional regeneration and two alternative regeneration cycle configurations were examined. In contrast to air dilution, CO2 -diluted cycle efficiencies increased by approximately 1.0 percentage point for the three regeneration configurations examined, while the efficiency of the CO2-diluted simple cycle decreased by approximately 5.0 percentage points. For CO2-diluted cycles with a closed-exhaust recycling path, an optimum CO2-recycle pressure was determined for each configuration that was significantly lower than atmospheric pressure. Un-cooled alternative regeneration configurations with CO2 recycling achieved efficiencies near 50%, which was approximately 3.0 percentage points higher than the conventional regeneration cycle and simple cycle configurations that utilized CO2 recycling. Accounting for cooling of the first two turbine stages resulted in a 2--3 percentage point reduction in un-cooled efficiency, with air dilution corresponding to the upper extreme. Additionally, when the work required to sequester CO2 was accounted for, cooled cycle efficiency decreased by 4--6 percentage points, and was more negatively impacted when syngas fuels were used. Finally, turbine design models showed that turbine blades are shorter with CO2 dilution, resulting in fewer design restrictions.

Release of Dissolved CO2 from Water in Laboratory Porous Media Following Rapid Depressurization

NASA Astrophysics Data System (ADS)

Crews, J. B.; Cooper, C. A.

2011-12-01

A bench-top laboratory study is undertaken to investigate the effects of seismic shocks on brine aquifers into which carbon dioxide has been injected for permanent storage. Long-term storage in deep saline aquifers has been proposed and studied as one of the most viable near-term options for sequestering fossil fuel-derived carbon dioxide from the atmosphere to curb anthropogenic climate change. Upon injection into the subsurface, it is expected that CO2, as either a gas or supercritical fluid, will mix convectively with the formation water. The possibility exists, however, that dissolved CO2 will come out of solution as a result of an earthquake. The effect is similar to that of slamming an unsealed container of carbonated beverage on a table; previously dissolved CO2 precipitates, forms bubbles, and rises due to buoyancy. In this study, we measure the change in gas-phase CO2 concentration as a function of the magnitude of the shock and the initial concentration of CO2. In addition, we investigate and seek to characterize the nucleation and transport of CO2 bubbles in a porous medium after a seismic shock. Experiments are conducted using a Hele-Shaw cell and a CCD camera to quantify the fraction of dissolved CO2 that comes out of solution as a result of a sharp mechanical impulse. The data are used to identify and constrain the conditions under which CO2 comes out of solution and, further, to understand the end-behavior of the precipitated gas-phase CO2 as it moves through or is immobilized in a porous medium.

Inorganic carbon and fossil organic carbon are source of bias for quantification of sequestered carbon in mine spoil

NASA Astrophysics Data System (ADS)

Vindušková, Olga; Frouz, Jan

2016-04-01

Carbon sequestration in mine soils has been studied as a possibility to mitigate the rising atmospheric CO2 levels and to improve mine soil quality (Vindu\\vsková and Frouz, 2013). Moreover, these soils offer an unique opportunity to study soil carbon dynamics using the chronosequence approach (using a set of sites of different age on similar parent material). However, quantification of sequestered carbon in mine soils is often complicated by fossil organic carbon (e.g., from coal or kerogen) or inorganic carbon present in the spoil. We present a methodology for quantification of both of these common constituents of mine soils. Our recommendations are based on experiments done on post-mining soils in Sokolov basin, Czech Republic. Here, fossil organic carbon is present mainly as kerogen Type I and II and represents 2-6 wt.% C in these soils. Inorganic carbon in these soils is present mainly as siderite (FeCO3), calcite (CaCO3), and dolomite (CaMg(CO3)2). All of these carbonates are often found in the overburden of coal seams thus being a common constituent of post-mining soils in the world. Vindu\\vsková O, Frouz J, 2013. Soil carbon accumulation after open-cast coal and oil shale mining in Northern Hemisphere: a quantitative review. ENVIRONMENTAL EARTH SCIENCES, 69: 1685-1698. Vindu\\vsková O, Dvořáček V, Prohasková A, Frouz J. 2014. Distinguishing recent and fossil organic matter - A critical step in evaluation of post-mining soil development - using near infrared spectroscopy. ECOLOGICAL ENGINEERING. 73: 643-648. Vindu\\vsková O, Sebag D, Cailleau G, Brus J, Frouz J. 2015. Methodological comparison for quantitative analysis of fossil and recently derived carbon in mine soils with high content of aliphatic kerogen. ORGANIC GEOCHEMISTRY, 89-90:14-22.

USE OF SUPPLEMENTARY CEMENTITIOUS MATERIALS IN HIGH PERFORMANCE, CO2 SEQUESTERING CONSTRUCTION MATERIAL - PHASE I

EPA Science Inventory

The impact of long-term changes in water table height on carbon cycling in sub-boreal peatlands

NASA Astrophysics Data System (ADS)

Pypker, T. G.; Moore, P. A.; Waddington, J. M.; Hribljan, J. A.; Ballantyne, D.; Chimner, R. A.

2011-12-01

Peatlands are a critical component in the global carbon (C) cycle because they have been slowly sequestering atmospheric greenhouse gases as peat since the last glaciation. Today, soil C stocks in peatlands are estimated to represent 224 to 455 Pg, equal to 12-30% of the global soil C pool. At present, peatlands are estimated to sequester 76 Tg C yr-1. The flux of C to and from peatlands is likely to respond to climate change, thereby influencing atmospheric C concentrations. Peatland C budgets are tightly linked to their hydrology, hence, it is critical we understand how changes in hydrology will affect the C budgets of peatlands. The main objective of the project was to determine how long-term changes in water table height affect CO2 and CH4 fluxes from three adjacent peatlands. This study took place in the Seney National Wildlife Refuge (SNWR) in the Upper Peninsula of Michigan. SNWR is home to the largest wetland drainage project in Michigan. In 1912, ditches and dikes were created in an effort to convert approximately 20,000 ha of peatland to agriculture. The ditches and dikes were unsuccessful in creating agricultural land, but they are still in place. The manipulation of water table heights provides an opportunity to research how long-term peat drying or wetting alters C cycling in peatlands. From May to November in 2009, 2010 and 2011, we monitored CO2 fluxes using eddy covariance and chamber techniques in three adjacent peatlands with lowered, relatively unaltered ("control") and raised water table heights. In 2011, we installed CH4 analyzers to continuously monitor CH4 fluxes at the sites with high and relatively unaltered water table heights. The results are compared across sites to determine how changes in water table height might affect C fluxes sub-boreal peatlands.

Development of Carbon Sequestration Options by Studying Carbon Dioxide-Methane Exchange in Hydrates

NASA Astrophysics Data System (ADS)

Horvat, Kristine Nicole

Gas hydrates form naturally at high pressures (>4 MPa) and low temperatures (<4 °C) when a set number of water molecules form a cage in which small gas molecules can be entrapped as guests. It is estimated that about 700,000 trillion cubic feet (tcf) of methane (CH4) exist naturally as hydrates in marine and permafrost environments, which is more than any other natural sources combined as CH4 hydrates contain about 14 wt% CH4. However, a vast amount of gas hydrates exist in marine environments, which makes gas extraction an environmental challenge, both for potential gas losses during extraction and the potential impact of CH4 extraction on seafloor stability. From the climate change point of view, a 100 ppm increase in atmospheric carbon dioxide (CO2) levels over the past century is of urgent concern. A potential solution to both of these issues is to simultaneously exchange CH4 with CO 2 in natural hydrate reserves by forming more stable CO2 hydrates. This approach would minimize disturbances to the host sediment matrix of the seafloor while sequestering CO2. Understanding hydrate growth over time is imperative to prepare for large scale CH4 extraction coupled with CO2 sequestration. In this study, we performed macroscale experiments in a 200 mL high-pressure Jerguson cell that mimicked the pressure-temperature conditions of the seafloor. A total of 13 runs were performed under varying conditions. These included the formation of CH4 hydrates, followed by a CO2 gas injection and CO2 hydrate formation followed by a CH4 gas injection. Results demonstrated that once gas hydrates formed, they show "memory effect" in subsequent charges, irrespective of the two gases injected. This was borne out by the induction time data for hydrate formation that reduced from 96 hours for CH4 and 24 hours for CO2 to instant hydrate formation in both cases upon injection of a secondary gas. During the study of CH4-CO2 exchange where CH4 hydrates were first formed and CO2 gas was injected into the system, gas chromatographic (GC) analysis of the cell indicated a pure CH4 gas phase, i.e., all injected CO2 gas entered the hydrate phase and remained trapped in hydrate cages for several hours, though over time some CO2 did enter the gas phase. Alternatively, during the CH 4-CO2 exchange study where CO2 hydrates were first formed, the injected CH4 initially entered the hydrate phase, but quickly gaseous CO2 exchanged with CH4 in hydrates to form more stable CO2 hydrates. These results are consistent with the better thermodynamic stability of CO2 hydrates, and this appears to be a promising method to sequester CO2 in natural CH4 hydrate matrices. The macroscale study described above was complemented by a microscale study to visualize hydrate growth. This first-of-its-kind in-situ study utilized the x-ray computed microtomography (CMT) technique to visualize microscale CO2, CH4, and mixed CH 4-CO2 hydrate growth phenomenon in salt solutions in the presence or absence of porous media. The data showed that under the experimental conditions used, pure CH4 formed CH4 hydrates as mostly spheres, while pure CO2 hydrates were more dendritic branches. Additionally, varying ratios of mixed CH4-CO2 hydrates were also formed that had needle-like growth. In porous media, CO2 hydrates grew, consistent with known growth models in which the solution was the sediment wetting phase. When glass beads and Ottawa sand were used as a host, the system exhibited pore-filling hydrate growth, while the presence of liquid CO2 and possible CO2 hydrates in Ottawa sand initially were pore-filling that over time transformed into a grain-displacing morphology. The data appears promising to develop a method that would supplant our energy supply by extracting CH4 from naturally occurring hydrates while CO2 is sequestered in the same formations.

Mineralogical and geochemical consequences of the long-term presence of CO2 in natural reservoirs: An example from the Springerville-St. Johns Field, Arizona, and New Mexico, U.S.A

USGS Publications Warehouse

Moore, J.; Adams, M.; Allis, R.; Lutz, S.; Rauzi, S.

2005-01-01

The Springerville-St. Johns CO2 field in eastern Arizona and western New Mexico is one of more than a dozen gas fields developed within the Colorado Plateau and Southern Rocky Mountain region. Extensive travertine (CaCO3) deposits record a long history of CO2 migration and leakage to the atmosphere. The oldest travertine deposits may have formed during the initial filling of the CO2 reservoir when groundwaters exsolved CO2 upon reaching the surface. The youngest travertine deposits are associated with springs on the floor of the Little Colorado River valley, but travertine deposition appears to be insignificant today. Older deposits occur up to 325 m above the valley floor. Geologic relationships suggest travertine deposition began in the late Pleistocene after volcanic activity ended at ???0.3 Ma. Most of the CaCO3 could have been derived from dissolution of the underlying limestones and dolomites. Interactions between the reservoir fluids and rocks were observed in core samples from one of the intervals that produced dry gas. These reactions resulted in the dissolution of carbonate cements and detrital feldspars and the formation of dawsonite and kaolinite. Geochemical simulations suggest that the dawsonite could have been deposited when the CO2 fugacity reached 20 bars and that the kaolinite formed as the CO2 fugacity decreased. Corrosion of drill pipe by acidic waters and a pronounced HCO3 anomaly above the CO2 reservoir provide evidence of a continuing flux of CO2 from depth. CO2 storage occurs primarily as dissolved carbonate species and as gas accumulations. Only a small percentage of the CO2 was sequestered in secondary minerals. ?? 2005 Elsevier B.V. All rights reserved.

Trace contaminant concentration affects mineral transformation and pollutant fate in hydroxide-weathered Hanford sediments.

PubMed

Perdrial, Nicolas; Rivera, Nelson; Thompson, Aaron; O'Day, Peggy A; Chorover, Jon

2011-12-15

Prior work has shown that when silicaceous sediments are infused with caustic radioactive waste, contaminant fate is tightly coupled to ensuing mineral weathering reactions. However, the effects of local aqueous geochemical conditions on these reactions are poorly studied. Thus, we varied contaminant concentration and pCO(2) during the weathering of previously uncontaminated Hanford sediments over 6 months and 1 year in a solution of caustic waste (pH 13, high ionic strength). Co-contaminants Sr, Cs and I were added at "low" (Cs/Sr: 10(-5)m; I: 10(-7)m) and "high" (Cs/Sr: 10(-3)m; I: 10(-5)m) concentrations, and headspace was held at atmospheric or undetectable (<10ppmv) CO(2) partial pressure. Solid phase characterization revealed the formation of the zeolite chabazite in "high" samples, whereas feldspathoids, sodalite and cancrinite, were formed preferentially in "low" samples. Sr, Cs and I were sequestered in all reacted sediments. Native calcite dissolution in the CO(2)-free treatment drove the formation of strätlingite (Ca(2)Al(2)SiO(7)·8H(2)O) and diminished availability of Si and Al for feldspathoid formation. Results indicate that pCO(2) and contaminant concentrations strongly affect contaminant speciation in waste-weathered sediments, and are therefore likely to impact reaction product stability under any remediation scenario. Copyright © 2011 Elsevier B.V. All rights reserved.

Biotic and abiotic effects on CO2 sequestration during microbially-induced calcium carbonate precipitation.

PubMed

Okyay, Tugba Onal; Rodrigues, Debora F

2015-03-01

In this study, CO2 sequestration was investigated through the microbially-induced calcium carbonate precipitation (MICP) process with isolates obtained from a cave called 'Cave Without A Name' (Boerne, TX, USA) and the Pamukkale travertines (Denizli, Turkey). The majority of the bacterial isolates obtained from these habitats belonged to the genera Sporosarcina, Brevundimonas, Sphingobacterium and Acinetobacter. The isolates were investigated for their capability to precipitate calcium carbonate and sequester CO2. Biotic and abiotic effects of CO2 sequestration during MICP were also investigated. In the biotic effect, we observed that the rate and concentration of CO2 sequestered was dependent on the species or strains. The main abiotic factors affecting CO2 sequestration during MICP were the pH and medium components. The increase in pH led to enhanced CO2 sequestration by the growth medium. The growth medium components, on the other hand, were shown to affect both the urease activity and CO2 sequestration. Through the Plackett-Burman experimental design, the most important growth medium component involved in CO2 sequestration was determined to be urea. The optimized medium composition by the Plackett-Burman design for each isolate led to a statistically significant increase, of up to 148.9%, in CO2 uptake through calcification mechanisms. © FEMS 2015. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Iron, phytoplankton growth, and the carbon cycle.

PubMed

Street, Joseph H; Paytan, Adina

2005-01-01

Iron is an essential nutrient for all living organisms. Iron is required for the synthesis of chlorophyll and of several photosynthetic electron transport proteins and for the reduction of CO2, SO4(2-), and NO3(-) during the photosynthetic production of organic compounds. Iron concentrations in vast areas of the ocean are very low (<1 nM) due to the low solubility of iron in oxic seawater. Low iron concentrations have been shown to limit primary production rates, biomass accumulation, and ecosystem structure in a variety of open-ocean environments, including the equatorial Pacific, the subarctic Pacific and the Southern Ocean and even in some coastal areas. Oceanic primary production, the transfer of carbon dioxide into organic carbon by photosynthetic plankton (phytoplankton), is one process by which atmospheric CO2 can be transferred to the deep ocean and sequestered for long periods of time. Accordingly, iron limitation of primary producers likely plays a major role in the global carbon cycle. It has been suggested that variations in oceanic primary productivity, spurred by changes in the deposition of iron in atmospheric dust, control atmospheric CO2 concentrations, and hence global climate, over glacial-interglacial timescales. A contemporary application of this "iron hypothesis" promotes the large-scale iron fertilization of ocean regions as a means of enhancing the ability of the ocean to store anthropogenic CO2 and mitigate 21st century climate change. Recent in situ iron enrichment experiments in the HNLC regions, however, cast doubt on the efficacy and advisability of iron fertilization schemes. The experiments have confirmed the role of iron in regulating primary productivity, but resulted in only small carbon export fluxes to the depths necessary for long-term sequestration. Above all, these experiments and other studies of iron biogeochemistry over the last two decades have begun to illustrate the great complexity of the ocean system. Attempts to engineer this system are likely to provoke a similarly complex, unpredictable response.

Reversible interconversion of carbon dioxide and formate by an electroactive enzyme

PubMed Central

Reda, Torsten; Plugge, Caroline M.; Abram, Nerilie J.; Hirst, Judy

2008-01-01

Carbon dioxide (CO2) is a kinetically and thermodynamically stable molecule. It is easily formed by the oxidation of organic molecules, during combustion or respiration, but is difficult to reduce. The production of reduced carbon compounds from CO2 is an attractive proposition, because carbon-neutral energy sources could be used to generate fuel resources and sequester CO2 from the atmosphere. However, available methods for the electrochemical reduction of CO2 require excessive overpotentials (are energetically wasteful) and produce mixtures of products. Here, we show that a tungsten-containing formate dehydrogenase enzyme (FDH1) adsorbed to an electrode surface catalyzes the efficient electrochemical reduction of CO2 to formate. Electrocatalysis by FDH1 is thermodynamically reversible—only small overpotentials are required, and the point of zero net catalytic current defines the reduction potential. It occurs under thoroughly mild conditions, and formate is the only product. Both as a homogeneous catalyst and on the electrode, FDH1 catalyzes CO2 reduction with a rate more than two orders of magnitude faster than that of any known catalyst for the same reaction. Formate oxidation is more than five times faster than CO2 reduction. Thermodynamically, formate and hydrogen are oxidized at similar potentials, so formate is a viable energy source in its own right as well as an industrially important feedstock and a stable intermediate in the conversion of CO2 to methanol and methane. FDH1 demonstrates the feasibility of interconverting CO2 and formate electrochemically, and it is a template for the development of robust synthetic catalysts suitable for practical applications. PMID:18667702

Fireside corrosion in oxy-fuel combustion of coal

DOE PAGES

Holcomb, Gordon R.; Tylczak, Joseph; Meier, Gerald H.; ...

2011-08-01

Oxy-fuel combustion is based on burning fossil fuels in a mixture of recirculated flue gas and oxygen, rather than in air. An optimized oxy-combustion power plant will have ultra-low emissions since the flue gas that results from oxy-fuel combustion consists almost entirely of CO2 and water vapor. Once the water vapor is condensed, it is relatively easy to sequester the CO2 so that it does not escape into the atmosphere. A variety of laboratory tests comparing air-firing to oxy-firing conditions, and tests examining specific simpler combinations of oxidants, were conducted at 650-700 C. Alloys studied included model Fe-Cr and Ni-Crmore » alloys, commercial ferritic steels, austenitic steels, and nickel base superalloys. Furthermore, the observed corrosion behavior shows accelerated corrosion even with sulfate additions that remain solid at the tested temperatures, encapsulation of ash components in outer iron oxide scales, and a differentiation between oxy-fuel combustion flue gas recirculation choices.« less

Negative Emissions Technology

NASA Astrophysics Data System (ADS)

Day, Danny

2006-04-01

Although `negative emissions' of carbon dioxide need not, in principle, involve use of biological processes to draw carbon out of the atmosphere, such `agricultural' sequestration' is the only known way to remove carbon from the atmosphere on time scales comparable to the time scale for anthropogenic increases in carbon emissions. In order to maintain the `negative emissions' the biomass must be used in such a way that the resulting carbon dioxide is separated and permanently sequestered. Two options for sequestration are in the topsoil and via geologic carbon sequestration. The former has multiple benefits, but the latter also is needed. Thus, although geologic carbon sequestration is viewed skeptically by some environmentalists as simply a way to keep using fossil fuels---it may be a key part of reversing accelerating climate forcing if rapid climate change is beginning to occur. I will first review the general approach of agricultural sequestration combined with use of resulting biofuels in a way that permits carbon separation and then geologic sequestration as a negative emissions technology. Then I discuss the process that is the focus of my company---the EPRIDA cycle. If deployed at a sufficiently large scale, it could reverse the increase in CO2 concentrations. I also estimate of benefits --carbon and other---of large scale deployment of negative emissions technologies. For example, using the EPRIDA cycle by planting and soil sequestering carbon in an area abut In 3X the size of Texas would remove the amount of carbon that is being accumulated worldwide each year. In addition to the atmospheric carbon removal, the EPRIDA approach also counters the depletion of carbon in the soil---increasing topsoil and its fertility; reduces the excess nitrogen in the water by eliminating the need for ammonium nitrate fertilizer and reduces fossil fuel reliance by providing biofuel and avoiding natural gas based fertilizer production.

Monitoring field scale CO2 injection from time-lapse seismic and well log, integrating with advanced rock physics model at Cranfield EOR site

NASA Astrophysics Data System (ADS)

Ghosh, Ranjana

2017-12-01

Causes and effects of global warming have been highly debated in recent years. Nonetheless, injection and storage of CO2 (CO2 sequestration) in the subsurface is becoming increasingly accepted as a viable tool to reduce the amount of CO2 from the atmosphere, which is a primary contributor to global warming. Monitoring of CO2 movement with time is essential to ascertain that sequestration is not hazardous. A method is proposed here to appraise CO2 saturation from seismic attributes using differential effective medium theory modified for pressure (PDEM). The PDEM theory accounts pressure-induced fluid flow between cavities, which is a very important investigation in the CO2-sequestered regime of heterogeneous microstructure. The study area is the lower Tuscaloosa formation at Cranfield in Mississippi, USA, which is one of the active enhanced oil recovery (EOR), and CO2 capture and storage (CCS) fields. Injection well (F1) and two observation wells (F2 and F3) are present close (within 112 m) to the detailed area of study for this region. Since the three wells are closely situated, two wells, namely injection well F1 and the furthest observation well F3, have been focused on to monitor CO2 movement. Time-lapse (pre- and post-injection) log, core and surface seismic data are used in the quantitative assessment of CO2 saturation from the PDEM theory. It has been found that after approximately 9 months of injection, average CO2 saturations in F1 and F3 are estimated as 50% in a zone of thickness 25 m at a depth of 3 km.

Historical and future perspectives of global soil carbon response to climate and land-use changes

NASA Astrophysics Data System (ADS)

Eglin, T.; Ciais, P.; Piao, S. L.; Barre, P.; Bellassen, V.; Cadule, P.; Chenu, C.; Gasser, T.; Koven, C.; Reichstein, M.; Smith, P.

2010-11-01

ABSTRACT In this paper, we attempt to analyse the respective influences of land-use and climate changes on the global and regional balances of soil organic carbon (SOC) stocks. Two time periods are analysed: the historical period 1901-2000 and the period 2000-2100. The historical period is analysed using a synthesis of published data as well as new global and regional model simulations, and the future is analysed using models only. Historical land cover changes have resulted globally in SOC release into the atmosphere. This human induced SOC decrease was nearly balanced by the net SOC increase due to higher CO2 and rainfall. Mechanization of agriculture after the 1950s has accelerated SOC losses in croplands, whereas development of carbon-sequestering practices over the past decades may have limited SOC loss from arable soils. In some regions (Europe, China and USA), croplands are currently estimated to be either a small C sink or a small source, but not a large source of CO2 to the atmosphere. In the future, according to terrestrial biosphere and climate models projections, both climate and land cover changes might cause a net SOC loss, particularly in tropical regions. The timing, magnitude, and regional distribution of future SOC changes are all highly uncertain. Reducing this uncertainty requires improving future anthropogenic CO2 emissions and land-use scenarios and better understanding of biogeochemical processes that control SOC turnover, for both managed and un-managed ecosystems.

C balance, carbon dioxide emissions and global warming potentials in LCA-modelling of waste management systems.

PubMed

Christensen, Thomas H; Gentil, Emmanuel; Boldrin, Alessio; Larsen, Anna W; Weidema, Bo P; Hauschild, Michael

2009-11-01

Global warming potential (GWP) is an important impact category in life-cycle-assessment modelling of waste management systems. However, accounting of biogenic CO(2) emissions and sequestered biogenic carbon in landfills and in soils, amended with compost, is carried out in different ways in reported studies. A simplified model of carbon flows is presented for the waste management system and the surrounding industries, represented by the pulp and paper manufacturing industry, the forestry industry and the energy industry. The model calculated the load of C to the atmosphere, under ideal conditions, for 14 different waste management scenarios under a range of system boundary conditions and a constant consumption of C-product (here assumed to be paper) and energy production within the combined system. Five sets of criteria for assigning GWP indices to waste management systems were applied to the same 14 scenarios and tested for their ability to rank the waste management alternatives reflecting the resulting CO(2) load to the atmosphere. Two complete criteria sets were identified yielding fully consistent results; one set considers biogenic CO(2) as neutral, the other one did not. The results showed that criteria for assigning global warming contributions are partly linked to the system boundary conditions. While the boundary to the paper industry and the energy industry usually is specified in LCA studies, the boundary to the forestry industry and the interaction between forestry and the energy industry should also be specified and accounted for.

Assessing spatiotemporal changes in forest carbon turnover times in observational data and models

NASA Astrophysics Data System (ADS)

Yu, K.; Smith, W. K.; Trugman, A. T.; van Mantgem, P.; Peng, C.; Condit, R.; Anderegg, W.

2017-12-01

Forests influence global carbon and water cycles, biophysical land-atmosphere feedbacks, and atmospheric composition. The capacity of forests to sequester atmospheric CO2 in a changing climate depends not only on the response of carbon uptake (i.e., gross primary productivity) but also on the simultaneous change in carbon residence time. However, changes in carbon residence with climate change are uncertain, impacting the accuracy of predictions of future terrestrial carbon cycle dynamics. Here, we use long-term forest inventory data representative of tropical, temperate, and boreal forests; satellite-based estimates of net primary productivity and vegetation carbon stock; and six models from the Coupled Model Intercomparison Project Phase 5 (CMIP5) to investigate spatiotemporal trends in carbon residence time and its relation to climate. Forest inventory and satellite-based estimates of carbon residence time show a pervasive decreasing trend across global forests. In contrast, the CMIP5 models diverge in predicting historical and future trends in carbon residence time. Divergence across CMIP5 models indicate carbon turnover times are not well constrained by observations, which likely contributes to large variability in future carbon cycle projections.

Atmospheric carbon mineralization in an industrial-scale chrysotile mining waste pile.

PubMed

Nowamooz, Ali; Dupuis, J Christian; Beaudoin, Georges; Molson, John; Lemieux, Jean-Michel; Horswill, Micha; Fortier, Richard; Larachi, Faïçal; Maldague, Xavier; Constantin, Marc; Duchesne, Josee; Therrien, René

2018-06-12

Magnesium rich minerals that are abundant in ultramafic mining waste have the potential to be used as a safe and permanent sequestration solution for carbon dioxide (CO2). Our understanding of thermo-hydro-chemical regimes that govern this reaction at an industrial scale, however, has remained an important challenge to its widespread implementation. Through a year-long monitoring experiment performed at a 110Mt chrysotile waste pile, we have documented the existence of two distinct thermo-hydro-chemical regimes that control the ingress of CO2 and the subsequent mineral carbonation of the waste. The experimental results are supported by coupled free-air/porous media numerical flow and transport model that provides insights into optimization strategies to increase the efficiency of mineral sequestration at an industrial-scale. Although functioning passively under less than optimal conditions compared to lab-scale experiments, the 110Mt Thetford Mines pile is nevertheless estimated to be sequestering up to 100 tonnes of CO2 per year, with a potential total carbon capture capacity under optimal conditions of 3 Mt. Yearly, over 100 Mt of ultramafic mine waste suitable for mineral carbonation are generated by the global mining industry. Our results show that this waste material could become a safe and permanent carbon sink for diffuse sources of CO2.

Carbon sequestration via reaction with basaltic rocks: geochemical modeling and experimental results

USGS Publications Warehouse

Rosenbauer, Robert J.; Thomas, Burt; Bischoff, James L.; Palandri, James

2012-01-01

Basaltic rocks are potential repositories for sequestering carbon dioxide (CO2) because of their capacity for trapping CO2 in carbonate minerals. We carried out a series of thermodynamic equilibrium models and high pressure experiments, reacting basalt with CO2-charged fluids over a range of conditions from 50 to 200 °C at 300 bar. Results indicate basalt has a high reactivity to CO2 acidified brine. Carbon dioxide is taken up from solution at all temperatures from 50 to 200 °C, 300 bar, but the maximum extent and rate of reaction occurs at 100 °C, 300 bar. Reaction path simulations utilizing the geochemical modeling program CHILLER predicted an equilibrium carbonate alteration assemblage of calcite, magnesite, and siderite, but the only secondary carbonate identified in the experiments was a ferroan magnesite. The amount of uptake at 100 °C, 300 bar ranged from 8% by weight for a typical tholeite to 26% for a picrite. The actual amount of CO2 uptake and extent of rock alteration coincides directly with the magnesium content of the rock suggesting that overall reaction extent is controlled by bulk basalt Mg content. In terms of sequestering CO2, an average basaltic MgO content of 8% is equivalent to 2.6 × 108 metric ton CO2/km3 basalt.

Geoengineering impact of open ocean dissolution of olivine on atmospheric CO2, surface ocean pH and marine biology

NASA Astrophysics Data System (ADS)

Köhler, Peter; Abrams, Jesse F.; Völker, Christoph; Hauck, Judith; Wolf-Gladrow, Dieter A.

2013-03-01

Ongoing global warming induced by anthropogenic emissions has opened the debate as to whether geoengineering is a ‘quick fix’ option. Here we analyse the intended and unintended effects of one specific geoengineering approach, which is enhanced weathering via the open ocean dissolution of the silicate-containing mineral olivine. This approach would not only reduce atmospheric CO2 and oppose surface ocean acidification, but would also impact on marine biology. If dissolved in the surface ocean, olivine sequesters 0.28 g carbon per g of olivine dissolved, similar to land-based enhanced weathering. Silicic acid input, a byproduct of the olivine dissolution, alters marine biology because silicate is in certain areas the limiting nutrient for diatoms. As a consequence, our model predicts a shift in phytoplankton species composition towards diatoms, altering the biological carbon pumps. Enhanced olivine dissolution, both on land and in the ocean, therefore needs to be considered as ocean fertilization. From dissolution kinetics we calculate that only olivine particles with a grain size of the order of 1 μm sink slowly enough to enable a nearly complete dissolution. The energy consumption for grinding to this small size might reduce the carbon sequestration efficiency by ˜30%.

Energy efficiency and reduction of CO2 emissions from campsites management in a protected area.

PubMed

Del Moretto, Deny; Branca, Teresa Annunziata; Colla, Valentina

2018-09-15

Campsites can be a pollution source, mainly due to the energy consumption. In addition, the green areas, thanks to the direct CO 2 sequestration and the shading, indirectly prevent the CO 2 emissions related to energy consumption. The methodology presented in this paper allowed assessing the annual CO 2 emissions directly related to the campsite management and the consequent environmental impact in campsite clusters in Tuscany. The software i-Tree Canopy was exploited, enabling to evaluate in terms of "canopy" the tonnes of CO 2 sequestered by the vegetation within each campsite. Energy and water consumptions from 2012 to 2015 were assessed for each campsite. As far as the distribution of sequestered CO 2 is concerned, the campsites ranking was in accordance to their size. According to the indicator "T-Tree" or canopy cover, a larger area of the canopy cover allows using less outdoor areas covered by trees for the sequestration of the remaining amount of pollutants. The analysis shows that the considered campsites, that are located in a highly naturalistic Park, present significant positive aspects both in terms of CO 2 emission reductions and of energy efficiency. However, significant margins of improvement are also possible and they were analysed in the paper. Copyright © 2018 Elsevier Ltd. All rights reserved.

Redox-controlled carbon and phosphorus burial: A mechanism for enhanced organic carbon sequestration during the PETM

NASA Astrophysics Data System (ADS)

Komar, Nemanja; Zeebe, Richard E.

2017-12-01

Geological records reveal a major perturbation in carbon cycling during the Paleocene-Eocene Thermal Maximum (PETM, ∼56 Ma), marked by global warming of more than 5 °C and a prominent negative carbon isotope excursion of at least 2.5‰ within the marine realm. The entire event lasted about 200,000 yr and was associated with a massive release of light carbon into the ocean-atmosphere system over several thousands of years. Here we focus on the terminal stage of the PETM, during which the ocean-atmosphere system rapidly recovered from the carbon cycle perturbation. We employ a carbon-cycle box model to examine the feedbacks between surface ocean biological production, carbon, oxygen, phosphorus, and carbonate chemistry during massive CO2 release events, such as the PETM. The model results indicate that the redox-controlled carbon-phosphorus feedback is capable of producing enhanced organic carbon sequestration during large carbon emission events. The locale of carbon oxidation (ocean vs. atmosphere) does not affect the amount of carbon sequestered. However, even though the model produces trends consistent with oxygen, excess accumulation rates of organic carbon (∼1700 Pg C during the recovery stage), export production and δ13 C data, it fails to reproduce the magnitude of change of sediment carbonate content and the CCD over-deepening during the recovery stage. The CCD and sediment carbonate content overshoot during the recovery stage is muted by a predicted increase in CaCO3 rain. Nonetheless, there are indications that the CaCO3 export remained relatively constant during the PETM. If this was indeed true, then an initial pulse of 3,000 Pg C followed by an additional, slow leak of 2,500 Pg C could have triggered an accelerated nutrient supply to the surface ocean instigating enhanced organic carbon export, consequently increasing organic carbon sequestration, resulting in an accelerated restoration of ocean-atmosphere biogeochemistry during the termination phase of the PETM.

Magmatic volatiles and the weathering of Mars

NASA Technical Reports Server (NTRS)

Clark, B. C.

1993-01-01

The sources for volatiles on Mars have been the subject of many hypotheses for exogenous influences including late accretion of volatile-enriched material, impact devolatilization to create massive early atmospheres, and even major bombardment by comets. However, the inventory of chemically active volatiles observable at the contemporary surface of Mars is consistent with domination by endogenous, subsequent planetary processes, viz., persistent magmatic outgassing. Volcanism on Mars has been widespread in both space and time. Notwithstanding important specific differences between the mantles of Earth and Mars, the geochemical similarities are such that the suite of gases emitted from Martian volcanic activity should include H2O, CO2, S-containing gases (e.g. H2S and/or SO2), and Cl-containing gases (e.g., Cl2 and/or HCl). H2O and CO2 exist in the atmosphere of Mars. Both are also present as surface condensates. However, spectroscopic observations of the Martian atmosphere clearly show that the S- and Cl-containing gases are severely depleted, with upper limits of less than or equal to 10(exp -7) the abundance of CO2. Likewise, there is no evidence of polar condensates of compounds of these elements as there is for CO2 and H2O. Within the soil, on the other hand, there has been direct measurement of incorporated H2O and abundant compounds containing S and Cl. Barring some as yet implausible geochemical sequestering process, the S/Cl ratio of about 6:1 in Martian soils implies a limit of 5% on the contribution of matter of solarlike composition (e.g., carbonaceous chondrite or cometary material) to these volatiles. Hence, exogenous sources are minor or not yet observed. From analysis of elemental trends in Martian soils, it has been recently shown that a simple two-component model can satisfy the Viking in situ measurements. Component A includes Si and most or all the Al, Ca, Ti, and Fe. Component B, taken as 16 +/- 3% by weight of the total, contains S and most or all the Cl and Mg. These results constrain several models of Martian soil mineralogy but are consistent with a mixture of silicates (such as Fe-rich clays and accessory minerals and soluble salts). The overall element profile is notably like shergottites, with significant incorporation of chemically reactive atmospheric gases from magmatic degassing.

Genome Sequence of Carbon Dioxide-Sequestering Serratia sp. Strain ISTD04 Isolated from Marble Mining Rocks.

PubMed

Kumar, Manish; Gazara, Rajesh Kumar; Verma, Sandhya; Kumar, Madan; Verma, Praveen Kumar; Thakur, Indu Shekhar

2016-10-20

The Serratia sp. strain ISTD04 has been identified as a carbon dioxide (CO 2 )-sequestering bacterium isolated from marble mining rocks in the Umra area, Rajasthan, India. This strain grows chemolithotrophically on media that contain sodium bicarbonate (NaHCO 3 ) as the sole carbon source. Here, we report the genome sequence of 5.07 Mb Serratia sp. ISTD04. Copyright © 2016 Kumar et al.

The effect of Sphagnum farming on the greenhouse gas balance of donor and propagation areas, irrigation polders and commercial cultivation sites

NASA Astrophysics Data System (ADS)

Oestmann, Jan; Tiemeyer, Bärbel

2017-04-01

Drainage of peatlands for agriculture, forestry and peat extraction turned these landscapes into hotspots of greenhouse gas emissions. Climate protection now fosters rewetting projects to restore the natural peatland function as a sink of atmospheric carbon. One possible way to combine ecological and economical goals is Sphagnum farming, i.e. the cultivation of Sphagnum mosses as high-quality substrates for horticulture. This project scientifically evaluates the attempt of commercial Sphagnum farming on former peat extraction sites in north-western Germany. The exchange of carbon dioxide (CO2), methane (CH4) and nitrous oxide (N2O) of the whole peatland-based production chain comprising a donor mire, a propagation area, an irrigation polder and a cultivation site will be determined in a high temporal resolution for two years using manual chambers. This will allow evaluating the greenhouse gas balance of Sphagnum farming sites in comparison to near-natural sites and the potential of Sphagnum farming for restoring drained peatlands to sinks of atmospheric carbon. The influence of different irrigation techniques will also be tested. Additionally, selected plots will be equipped with open top chambers in order to examine the greenhouse gas exchange under potential future climate change conditions. Finally, a 13C pulse labeling experiment will make it possible to trace the newly sequestered CO2 in biomass, soil, respiration and dissolved organic carbon.

Extraction of extracellular lipids from chemoautotrophic bacteria Serratia sp. ISTD04 for production of biodiesel.

PubMed

Bharti, Randhir K; Srivastava, Shaili; Thakur, Indu Shekhar

2014-08-01

A CO2 sequestering bacterial strain, Serratia sp. ISTD04, that produces a significant amount of extracellular lipids was isolated from marble mine rocks. (14)C labeling analysis revealed that the rate of assimilation of CO2 by the strain is 0.756×10(-9)μmolCO2fixedcell(-1)h(-1). It was found to produce 466mg/l of extracellular lipid which was characterized using (1)H NMR. After transesterification of lipids, the total saturated and unsaturated FAME was found to be 51% and 49% respectively. The major FAME contained in the biodiesel were palmitic acid methyl ester (C16:0), oleic acid methyl ester (C18:1) and 10-nonadecenoic acid methyl ester (C19:1). Biodiesel produced by Serratia sp. ISTD04 is balanced in terms of FAME composition of good quality. It also contained higher proportion of oleic acid (35%) which makes it suitable for utilization in existing engines. Thus, the strain can be harnessed commercially to sequester CO2 into biodiesel. Copyright © 2014 Elsevier Ltd. All rights reserved.

Leakage Risk Assessment for a Potential CO2 Storage Project in Saskatchewan, Canada

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

Houseworth, J.E.; Oldenburg, C.M.; Mazzoldi, A.

2011-05-01

A CO{sub 2} sequestration project is being considered to (1) capture CO{sub 2} emissions from the Consumers Cooperative Refineries Limited at Regina, Saskatchewan and (2) geologically sequester the captured CO{sub 2} locally in a deep saline aquifer. This project is a collaboration of several industrial and governmental organizations, including the Petroleum Technology Research Centre (PTRC), Sustainable Development Technology Canada (SDTC), SaskEnvironment Go Green Fund, SaskPower, CCRL, Schlumberger Carbon Services, and Enbridge. The project objective is to sequester 600 tonnes CO{sub 2}/day. Injection is planned to start in 2012 or 2013 for a period of 25 years for a total storagemore » of approximately 5.5 million tonnes CO{sub 2}. This report presents an assessment of the leakage risk of the proposed project using a methodology known as the Certification Framework (CF). The CF is used for evaluating CO{sub 2} leakage risk associated with geologic carbon sequestration (GCS), as well as brine leakage risk owing to displacement and pressurization of brine by the injected CO{sub 2}. We follow the CF methodology by defining the entities (so-called Compartments) that could be impacted by CO{sub 2} leakage, the CO{sub 2} storage region, the potential for leakage along well and fault pathways, and the consequences of such leakage. An understanding of the likelihood and consequences of leakage forms the basis for understanding CO{sub 2} leakage risk, and forms the basis for recommendations of additional data collection and analysis to increase confidence in the risk assessment.« less

Glacial greenhouse-gas fluctuations controlled by ocean circulation changes.

PubMed

Schmittner, Andreas; Galbraith, Eric D

2008-11-20

Earth's climate and the concentrations of the atmospheric greenhouse gases carbon dioxide (CO(2)) and nitrous oxide (N(2)O) varied strongly on millennial timescales during past glacial periods. Large and rapid warming events in Greenland and the North Atlantic were followed by more gradual cooling, and are highly correlated with fluctuations of N(2)O as recorded in ice cores. Antarctic temperature variations, on the other hand, were smaller and more gradual, showed warming during the Greenland cold phase and cooling while the North Atlantic was warm, and were highly correlated with fluctuations in CO(2). Abrupt changes in the Atlantic meridional overturning circulation (AMOC) have often been invoked to explain the physical characteristics of these Dansgaard-Oeschger climate oscillations, but the mechanisms for the greenhouse-gas variations and their linkage to the AMOC have remained unclear. Here we present simulations with a coupled model of glacial climate and biogeochemical cycles, forced only with changes in the AMOC. The model simultaneously reproduces characteristic features of the Dansgaard-Oeschger temperature, as well as CO(2) and N(2)O fluctuations. Despite significant changes in the land carbon inventory, CO(2) variations on millennial timescales are dominated by slow changes in the deep ocean inventory of biologically sequestered carbon and are correlated with Antarctic temperature and Southern Ocean stratification. In contrast, N(2)O co-varies more rapidly with Greenland temperatures owing to fast adjustments of the thermocline oxygen budget. These results suggest that ocean circulation changes were the primary mechanism that drove glacial CO(2) and N(2)O fluctuations on millennial timescales.

The Geologic Nitrogen Cycle

NASA Astrophysics Data System (ADS)

Johnson, B. W.; Goldblatt, C.

2013-12-01

N2 is the dominant gas in Earth's atmosphere, and has been so through the majority of the planet's history. Originally thought to only be cycled in significant amounts through the biosphere, it is becoming increasingly clear that a large degree of geologic cycling can occur as well. N is present in crustal rocks at 10s to 100s of ppm and in the mantle at 1s to perhaps 10s of ppm. In light of new data, we present an Earth-system perspective of the modern N cycle, an updated N budget for the silicate Earth, and venture to explain the evolution of the N cycle over time. In an fashion similar to C, N has a fast, biologically mediated cycle and a slower cycle driven by plate tectonics. Bacteria fix N2 from the atmosphere into bioavailable forms. N is then cycled through the food chain, either by direct consumption of N-fixing bacteria, as NH4+ (the primary waste form), or NO3- (the most common inorganic species in the modern ocean). Some organic material settles as sediment on the ocean floor. In anoxic sediments, NH4+ dominates; due to similar ionic radii, it can readily substitute for K+ in mineral lattices, both in sedimentary rocks and in oceanic lithosphere. Once it enters a subduction zone, N may either be volatilized and returned to the atmosphere at arc volcanoes as N2 or N2O, sequestered into intrusive igneous rocks (as NH4+?), or subducted deep into the mantle, likely as NH4+. Mounting evidence indicates that a significant amount of N may be sequestered into the solid Earth, where it may remain for long periods (100s m.y.) before being returned to the atmosphere/biosphere by volcanism or weathering. The magnitude fluxes into the solid Earth and size of geologic N reservoirs are poorly constrained. The size of the N reservoirs contained in the solid Earth directly affects the evolution of Earth's atmosphere. It is possible that N now sequestered in the solid Earth was once in the atmosphere, which would have resulted in a higher atmospheric pressure, and therefore strengthened the greenhouse effect by pressure broadening the absorption of greenhouse gases. In addition,the behaviour of N is dependent on redox conditions in the ocean, which have not been constant over time.

Changes in biocrust cover drive carbon cycle responses to climate change in drylands.

PubMed

Maestre, Fernando T; Escolar, Cristina; de Guevara, Mónica Ladrón; Quero, José L; Lázaro, Roberto; Delgado-Baquerizo, Manuel; Ochoa, Victoria; Berdugo, Miguel; Gozalo, Beatriz; Gallardo, Antonio

2013-12-01

Dryland ecosystems account for ca. 27% of global soil organic carbon (C) reserves, yet it is largely unknown how climate change will impact C cycling and storage in these areas. In drylands, soil C concentrates at the surface, making it particularly sensitive to the activity of organisms inhabiting the soil uppermost levels, such as communities dominated by lichens, mosses, bacteria and fungi (biocrusts). We conducted a full factorial warming and rainfall exclusion experiment at two semiarid sites in Spain to show how an average increase of air temperature of 2-3 °C promoted a drastic reduction in biocrust cover (ca. 44% in 4 years). Warming significantly increased soil CO2 efflux, and reduced soil net CO2 uptake, in biocrust-dominated microsites. Losses of biocrust cover with warming through time were paralleled by increases in recalcitrant C sources, such as aromatic compounds, and in the abundance of fungi relative to bacteria. The dramatic reduction in biocrust cover with warming will lessen the capacity of drylands to sequester atmospheric CO2 . This decrease may act synergistically with other warming-induced effects, such as the increase in soil CO2 efflux and the changes in microbial communities to alter C cycling in drylands, and to reduce soil C stocks in the mid to long term. © 2013 John Wiley & Sons Ltd.

Historical carbon emissions and uptake from the agricultural frontier of the Brazilian Amazon.

PubMed

Galford, Gillian L; Melillo, Jerry M; Kicklighter, David W; Mustard, John F; Cronin, Timothy W; Cerri, Carlos E P; Cerri, Carlos C

2011-04-01

Tropical ecosystems play a large and complex role in the global carbon cycle. Clearing of natural ecosystems for agriculture leads to large pulses of CO2 to the atmosphere from terrestrial biomass. Concurrently, the remaining intact ecosystems, especially tropical forests, may be sequestering a large amount of carbon from the atmosphere in response to global environmental changes including climate changes and an increase in atmospheric CO2. Here we use an approach that integrates census-based historical land use reconstructions, remote-sensing-based contemporary land use change analyses, and simulation modeling of terrestrial biogeochemistry to estimate the net carbon balance over the period 1901-2006 for the state of Mato Grosso, Brazil, which is one of the most rapidly changing agricultural frontiers in the world. By the end of this period, we estimate that of the state's 925 225 km2, 221 092 km2 have been converted to pastures and 89 533 km2 have been converted to croplands, with forest-to-pasture conversions being the dominant land use trajectory but with recent transitions to croplands increasing rapidly in the last decade. These conversions have led to a cumulative release of 4.8 Pg C to the atmosphere, with 80% from forest clearing and 20% from the clearing of cerrado. Over the same period, we estimate that the residual undisturbed ecosystems accumulated 0.3 Pg C in response to CO2 fertilization. Therefore, the net emissions of carbon from Mato Grosso over this period were 4.5 Pg C. Net carbon emissions from Mato Grosso since 2000 averaged 146 Tg C/yr, on the order of Brazil's fossil fuel emissions during this period. These emissions were associated with the expansion of croplands to grow soybeans. While alternative management regimes in croplands, including tillage, fertilization, and cropping patterns promote carbon storage in ecosystems, they remain a small portion of the net carbon balance for the region. This detailed accounting of a region's carbon balance is the type of foundation analysis needed by the new United Nations Collaborative Programmme for Reducing Emissions from Deforestation and Forest Degradation (REDD).

Evaluation of calcium-bearing material for treatment of CO2 leakage-induced pollution

NASA Astrophysics Data System (ADS)

Park, J.; Park, M.; Jeong, H. Y.

2017-12-01

Several Ca2+-bearing materials were evaluated for their capability to treat CO2 leakage-induced pollution for the application of permeable reactive barriers (PRBs). In this regard, a series of batch experiments were carried out with Portland cement, quick lime (CaO), and gypsum (CaSO4). Each of these materials was added to 50 mL of CO2-saturated solutions ( 7.5-8.5 mM) in serum vials sealed with Teflon-coated grey butyl stopper. Subsequently, the resultant batches were agitated at room temperature for 24 h. At predetermined intervals, each vial was sacrificed to monitor changes in pH, EC, and dissolved CO2 concentration. Despite the pH-neutralizing capacity, 0.15 g of Portland cement did not lower any dissolved CO2. When amended with 0.05 g of Ca(OH)2 or Mg(OH)2, the cement at this loading could sequester dissolved CO2, with the former being more effective. Even without such amendments, the cement at or greater than 0.2 g was shown to completely sequester dissolved CO2. In case of quick lime, its loading as low as 0.05 g instantaneously removed all dissolved CO2, which was also noted for Portland cement at 0.5 g. For gypsum, its loading at 0.12 g was not effective for immobilizing dissolved CO2. By both X-ray diffraction (XRD) and thermogravimetry (TG) analyses, the CO2 sequestration by Ca2+-bearing materials was found to be mainly due to the formation of calcite (CaCO3). Funding source: The "R&D Project on Environmental Management of Geologic CO2 Storage" from the KEITI (Project Number: 2014001810003).

The impact of extreme drought on the biofuel feedstock production

NASA Astrophysics Data System (ADS)

hussain, M.; Zeri, M.; Bernacchi, C.

2013-12-01

Miscanthus (Miscanthus x giganteus) and Switchgrass (Panicum virgatum) have been identified as the primary targets for second-generation cellulosic biofuel crops. Prairie managed for biomass is also considered as one of the alternative to conventional biofuel and promised to provide ecosystem services, including carbon sequestration. These perennial grasses possess a number of traits that make them desirable biofuel crops and can be cultivated on marginal lands or interspersed with maize and soybean in the Corn Belt region. The U.S. Corn Belt region is the world's most productive and expansive maize-growing region, approximately 20% of the world's harvested corn hectares are found in 12 Corn Belt states. The introduction of a second generation cellulosic biofuels for biomass production in a landscape dominated by a grain crop (maize) has potential implications on the carbon and water cycles of the region. This issue is further intensified by the uncertainty in the response of the vegetation to the climate change induced drought periods, as was seen during the extreme droughts of 2011 and 2012 in the Midwest. The 2011 and 2012 growing seasons were considered driest since the 1932 dust bowl period; temperatures exceeded 3.0 °C above the 50- year mean and precipitation deficit reached 50 %. The major objective of this study was to evaluate the drought responses (2011 and 2012) of corn and perennial species at large scale, and to determine the seasonability of carbon and water fluxes in the response of controlling factors. We measured net CO2 ecosystem exchange (NEE) and water fluxes of maize-maize-soybean, and perennial species such as miscanthus, switchgrass and mixture of prairie grasses, using eddy covariance in the University of Illinois energy farm at Urbana, IL. The data presented here were for 5 years (2008- 2012). In the first two years, higher NEE in maize led to large CO2 sequestration. NEE however, decreased in dry years, particularly in 2012. On the other hand, miscanthus, switchgrass, and to a lesser extent, prairie showed higher NEE and gross primary production (GPP) - a partitioned NEE component - than maize during 2012. Although miscanthus uses more water relative to maize (consumed 30 % more water), Net Ecosystem Carbon Balance (NECB) results show that it provides the greatest net benefits of sequestering atmospheric CO2 during drought. Our findings highlight the important role of perennial species in sustaining productivity and sequestering CO2 during drought, as compared to maize. We conclude that changing land use from row crops to perennial species will result in more sequestered carbon, even with drought stress, and will be more resilient to prolonged dry periods.

Evaluating Impacts of CO2 Gas Intrusion Into a Confined Sandstone aquifer: Experimental Results

DOE PAGES

Qafoku, Nikolla; Lawter, Amanda R.; Shao, Hongbo; ...

2014-12-31

Deep subsurface storage and sequestration of CO2 has been identified as a potential mitigation technique for rising atmospheric CO2 concentrations. Sequestered CO2 represents a potential risk to overlying aquifers if the CO2 leaks from the deep storage reservoir. Experimental and modeling work is required to evaluate potential risks to groundwater quality and develop a systematic understanding of how CO2 leakage may cause important changes in aquifer chemistry and mineralogy by promoting dissolution/precipitation, adsorption/desorption, and redox reactions. Sediments from the High Plains aquifer in Kansas, United States, were used in this investigation, which is part of the National Risk Assessment Partnershipmore » Program sponsored by the US Department of Energy. This aquifer was selected to be representative of consolidated sand and gravel/sandstone aquifers overlying potential CO2 sequestration repositories within the continental US. In this paper, we present results from batch experiments conducted at room temperature and atmospheric pressure with four High Plains aquifer sediments. Batch experiments simulate sudden, fast, and short-lived releases of the CO2 gas as would occur in the case of well failure during injection. Time-dependent release of major, minor, and trace elements were determined by analyzing the contacting solutions. Characterization studies demonstrated that the High Plains aquifer sediments were abundant in quartz and feldspars, and contained about 15 to 20 wt% montmorillonite and up to 5 wt% micas. Some of the High Plains aquifer sediments contained no calcite, while others had up to about 7 wt% calcite. The strong acid extraction tests confirmed that in addition to the usual elements present in most soils, rocks, and sediments, the High Plains aquifer sediments had appreciable amounts of As, Cd, Pb, Cu, and occasionally Zn, which potentially may be mobilized from the solid to the aqueous phase during or after exposure to CO2. However, the results from the batch experiments showed that the High Plains sediments mobilized only low concentrations of trace elements (potential contaminants), which were detected occasionally in the aqueous phase during these experiments. Importantly, these occurrences were more frequent in the calcite-free sediment. Results from these investigations provide useful information to support site selection, risk assessment, and public education efforts associated with geological CO2 storage and sequestration.« less

Southern Ocean biogeochemical control of glacial/interglacial carbon dioxide change

NASA Astrophysics Data System (ADS)

Sigman, D. M.

2014-12-01

In the effort to explain the lower atmospheric CO2 concentrations observed during ice ages, two of the first hypotheses involved redistributing dissolved inorganic carbon (DIC) within the ocean. Broecker (1982) proposed a strengthening of the ocean's biological pump during ice ages, which increased the dissolved inorganic carbon gradient between the dark, voluminous ocean interior and the surface ocean's sun-lit, wind-mixed layer. Boyle (1988) proposed a deepening in the ocean interior's pool of DIC associated with organic carbon regeneration, with its concentration maximum shifting from intermediate to abyssal depths. While not irrefutable, evidence has arisen that these mechanisms can explain much of the ice age CO2 reduction and that both were activated by changes in the Southern Ocean. In the Antarctic Zone, reduced exchange of water between the surface and the underlying ocean sequestered more DIC in the ocean interior (the biological pump mechanism). Dust-borne iron fertilization of the Subantarctic surface lowered CO2 partly by the biological pump mechanism and partly by Boyle's carbon deepening. Each mechanism owes a part of its CO2 effect to a transient increase in seafloor calcium carbonate dissolution, which raised the ice age ocean's alkalinity, causing it to absorb more CO2. However, calcium carbonate cycling also sets limits on these mechanisms and their CO2 effects, such that the combination of Antarctic and Subantarctic changes is needed to achieve the full (80-100 ppm) ice age CO2 decline. Data suggest that these changes began at different phases in the development of the last ice age, 110 and 70 ka, respectively, explaining a 40 ppm CO2 drop at each time. We lack a robust understanding of the potential causes for both the implied reduction in Antarctic surface/deep exchange and the increase in Subantarctic dust supply during ice ages. Thus, even if the evidence for these Southern Ocean changes were to become incontrovertible, conceptual gaps stand in the way of a theory of glacial cycles that includes Southern Ocean-driven CO2 change. There are more compelling proposals for the causes of deglacial change, with a sharp reduction in North Atlantic deep water formation implicated as a trigger of increased surface/deep exchange in the Antarctic and the resulting release of CO2 to the atmosphere.

Geological carbon budget of the Mackenzie River Basin: New insight from the oxidation of rock-derived organic carbon

NASA Astrophysics Data System (ADS)

Horan, K.; Hilton, R. G.; Dellinger, M.; Galy, V.; Gaillardet, J.; Tipper, E.; Selby, D. S.; Ottley, C. J.; Burton, K. W.

2016-12-01

Erosion and weathering transfer carbon between the atmosphere and lithospheric storage, thereby operating to modify Earth's long-term climate. Over millions of years, atmospheric carbon dioxide (CO2) is sequestered during the weathering of silicate minerals by carbonic acid, coupled to carbonate formation, and following the erosion of biospheric organic carbon and its burial in sediments. However, erosion and weathering also act together to release CO2 from the lithosphere. Erosion enhances the rate of oxidative weathering of organic carbon in rocks (petrogenic OC, OCpetro), which is a major CO2 source over geological time. In addition, oxidation of sulfide minerals can produce sulfuric acid that weathers carbonate minerals and results in transient CO2 release. Although these sources and sinks of CO2 are well recognised, limited case studies exist where they have been measured alongside each other. Here we calculate the geological carbon budget during weathering and erosion in the Mackenzie River Basin, Canada. The silicate weathering rate, carbonate weathering rate by sulfuric acid and the sedimentary burial of biospheric organic carbon have been constrained by prior work. Closing the long-term CO2 budget therefore requires us to quantify the OCpetro oxidation rate. To do this, we use dissolved rhenium (Re) concentrations as a proxy for OCpetro weathering using samples collected from 2009 to 2013. We normalise dissolved river Re concentrations to the rock Re concentration ([Re]diss/[Re]rock) to assess the variability in oxidative weathering efficiency. We find [Re]diss/[Re]rock ratios are 2-4 times lower than those calculated for rapidly eroding mountain catchments (e.g. Taiwan), which is consistent with a lower physical erosion rate in the Mackenzie Basin. By making assumptions about the concurrent mobility of Re and CO2 during OCpetro weathering we quantify the OCpetro weathering rate and constrain the associated CO2 flux to be 0.3 tC km-2 yr-1. The transient CO2 release by sulfuric acid driven carbonate weathering is 0.8 tC km-2 yr-1. Therefore, these two CO2 sources counter CO2 drawdown by silicate weathering (0.4 tC km-2 yr-1). Nevertheless, OCpetro oxidation does not negate the large CO2 sink driven by biospheric organic carbon erosion (2 tC km-2 yr-1), so the Mackenzie Basin is presently a CO2 sink.

Adaptive physiological response, carbon partitioning, and biomass production of Withania somnifera (L.) Dunal grown under elevated CO2 regimes.

PubMed

Sharma, Rupali; Singh, Hukum; Kaushik, Monica; Nautiyal, Raman; Singh, Ombir

2018-06-01

Winter cherry or Ashwagandha ( Withania somnifera ) is an important medicinal plant used in traditional and herbal medicine system. Yet, there is no information available on response of this plant to changing climatic conditions particularly elevated atmospheric CO 2 concentrations. Therefore, we conducted an experiment to examine the effect of elevated CO 2 concentrations (ECs) on Withania somnifera . The variations in traits of physiological adaptation, net primary productivity, carbon partitioning, morphology, and biomass in response to elevated CO 2 concentrations (ambient, 600 and 800 µmol mol -1 ) during one growth cycle were investigated within the open top chamber (OTC) facility in the foothill of the Himalayas, Dehardun, India. ECs significantly increased photosynthetic rate, transpiration rate, stomatal conductance, water use efficiency, soil respiration, net primary productivity and the carbon content of plant tissues (leaf, stem, and root), and soil carbon. Furthermore, ECs significantly enhanced biomass production (root and shoot), although declined night leaf respiration. Overall, it was summarized that photosynthesis, stomatal conductance, water use efficiency, leaf, and soil carbon and biomass increased under ECs rendering the physiological adaptation to the plant. Increased net primary productivity might facilitate mitigation effects by sequestering elevated levels of carbon dioxide. We advocate further studies to investigate the effects of ECs on the accumulation of secondary metabolites and health-promoting substances of this as well as other medicinal plants.

Sustainable fuel for the transportation sector

PubMed Central

Agrawal, Rakesh; Singh, Navneet R.; Ribeiro, Fabio H.; Delgass, W. Nicholas

2007-01-01

A hybrid hydrogen-carbon (H2CAR) process for the production of liquid hydrocarbon fuels is proposed wherein biomass is the carbon source and hydrogen is supplied from carbon-free energy. To implement this concept, a process has been designed to co-feed a biomass gasifier with H2 and CO2 recycled from the H2-CO to liquid conversion reactor. Modeling of this biomass to liquids process has identified several major advantages of the H2CAR process. (i) The land area needed to grow the biomass is <40% of that needed by other routes that solely use biomass to support the entire transportation sector. (ii) Whereas the literature estimates known processes to be able to produce ≈30% of the United States transportation fuel from the annual biomass of 1.366 billion tons, the H2CAR process shows the potential to supply the entire United States transportation sector from that quantity of biomass. (iii) The synthesized liquid provides H2 storage in an open loop system. (iv) Reduction to practice of the H2CAR route has the potential to provide the transportation sector for the foreseeable future, using the existing infrastructure. The rationale of using H2 in the H2CAR process is explained by the significantly higher annualized average solar energy conversion efficiency for hydrogen generation versus that for biomass growth. For coal to liquids, the advantage of H2CAR is that there is no additional CO2 release to the atmosphere due to the replacement of petroleum with coal, thus eliminating the need to sequester CO2. PMID:17360377

Sustainable fuel for the transportation sector.

PubMed

Agrawal, Rakesh; Singh, Navneet R; Ribeiro, Fabio H; Delgass, W Nicholas

2007-03-20

A hybrid hydrogen-carbon (H(2)CAR) process for the production of liquid hydrocarbon fuels is proposed wherein biomass is the carbon source and hydrogen is supplied from carbon-free energy. To implement this concept, a process has been designed to co-feed a biomass gasifier with H(2) and CO(2) recycled from the H(2)-CO to liquid conversion reactor. Modeling of this biomass to liquids process has identified several major advantages of the H(2)CAR process. (i) The land area needed to grow the biomass is <40% of that needed by other routes that solely use biomass to support the entire transportation sector. (ii) Whereas the literature estimates known processes to be able to produce approximately 30% of the United States transportation fuel from the annual biomass of 1.366 billion tons, the H(2)CAR process shows the potential to supply the entire United States transportation sector from that quantity of biomass. (iii) The synthesized liquid provides H(2) storage in an open loop system. (iv) Reduction to practice of the H(2)CAR route has the potential to provide the transportation sector for the foreseeable future, using the existing infrastructure. The rationale of using H(2) in the H(2)CAR process is explained by the significantly higher annualized average solar energy conversion efficiency for hydrogen generation versus that for biomass growth. For coal to liquids, the advantage of H(2)CAR is that there is no additional CO(2) release to the atmosphere due to the replacement of petroleum with coal, thus eliminating the need to sequester CO(2).

The Energy Future.

PubMed

Newman, John; Bonino, Christopher A; Trainham, James A

2018-06-07

The foreseeable energy future will be driven by economics of known technologies and the desire to reduce CO 2 emissions to the atmosphere. Renewable energy options are compared with each other and with the use of fossil fuels with carbon capture and sequestration (CCS). Economic analysis is used to determine the best of several alternatives. One can disagree on the detailed costs, including externalities such as climate change and air and water pollution. But the differences in capital and operating costs between known technologies are so significant that one can draw clear conclusions. Results show that renewable energy cannot compete with fossil fuels on a cost basis alone because energy is intrinsic to the molecule, except for hydroelectricity. However, fossil fuels are implicated in climate change. Using renewable energy exclusively, including transportation and electricity needs, could reduce the standard of living in the United States by 43% to 62%, which would correspond to the level in about 1970. If capture and sequester of CO 2 are implemented, the cost of using fossil fuels will increase, but they beat renewable energy handily as an economic way to produce clean energy.

Study on potential of carbon dioxide absorption in reinforced concrete beams

NASA Astrophysics Data System (ADS)

Bambroo, Vibhas; Gupta, Shipali; Bhoite, Pratik; Sekar, S. K.

2017-11-01

The global gas emission is keeping on increasing for which cement industry alone contributes 5%. The enormous water is required for curing of concrete in construction industry which can effectively be used for various purposes. The accelerated carbonation curing shows a way to reduce these emissions in a very effective way by sequestering it in concrete elements. In this research the effect of accelerated carbonation curing was checked on non-reinforced concrete elements (cubes) and reinforced concrete elements (prisms). The 100mm × 100mm × 100 mm cubes and 150mm × 150mm × 1200mm prisms were cast. They were CO2 cured for 4 and 8 hours and were tested for compressive strength and flexural strength test. The CO2 curing results showed 27.7% and 1.8% increase in strength of cubes and prisms, respectively when compared to water cured specimens. This early age strength through waste gas proves beneficial in terms of reducing in atmospheric pollution and saving the water which is a critical resource now-a-days.

Habitability from Tidally Induced Tectonics

NASA Astrophysics Data System (ADS)

Valencia, Diana; Tan, Vivian Yun Yan; Zajac, Zachary

2018-04-01

The stability of Earth’s climate on geological timescales is enabled by the carbon–silicate cycle that acts as a negative feedback mechanism stabilizing surface temperatures via the intake and outgassing of atmospheric carbon. On Earth, this thermostat is enabled by plate tectonics that sequesters outgassed CO2 back into the mantle via weathering and subduction at convergent margins. Here we propose a separate tectonic mechanism—vertical recycling—that can serve as the vehicle for CO2 outgassing and sequestration over long timescales. The mechanism requires continuous tidal heating, which makes it particularly relevant to planets in the habitable zone of M stars. Dynamical models of this vertical recycling scenario and stability analysis show that temperate climates stable over timescales of billions of years are realized for a variety of initial conditions, even as the M star dims over time. The magnitude of equilibrium surface temperatures depends on the interplay of sea weathering and outgassing, which in turn depends on planetary carbon content, so that planets with lower carbon budgets are favored for temperate conditions. The habitability of planets such as found in the Trappist-1 system may be rooted in tidally driven tectonics.

Effects of High Carbon Dioxide Soil-Gas Concentrations and Emission Rates From Mammoth Mountain, California, USA

NASA Astrophysics Data System (ADS)

Farrar, C. D.; Evans, W. C.

2006-12-01

High concentrations (90 vol %) of carbon dioxide (CO2) are present in shallow soils, and CO2 is emitted to the atmosphere at high rates (1,000 g/d/m2), in several locations around Mammoth Mountain. The CO2 emissions have been diffuse and at ambient temperature. CO2 in the soil has killed most of the coniferous forest in five areas totaling 35 ha around the north, west, and south sides of the mountain at altitudes between 2,600 and 3,000 m. Part of the CO2 has dissolved in ground water, causing acidic conditions and severely corroding steel casings in several wells. The high CO2 emission rates are implicated in the deaths of four people in the past eight years. During winter, a large quantity of CO2 is sequestered in the snow pack on parts of the mountain, posing potential dangers for winter recreation. One U.S. Forest Service campground has been closed and safety plans have been implemented by the local ski resort. Mammoth Mountain is a dormant Quaternary volcanic center, but overlies an area that has been affected by periods of magmatic unrest during the past two decades. Hypocenters of long-period earthquakes indicate that basaltic intrusions reach depths as shallow as 20 to 15 km, from which CO2 has exsolved during decompression and (or) crystallization of these intrusions. CO2 moves to the land surface along fracture zones associated with faults and possibly geologic contacts. The magmatic source of CO2 is confirmed by ¦Ä13C = -3 to -5 PDB, a lack of 14C, and 3He/4He = 4 to 5 R/RA. The present-day high CO2 soil-gas concentrations and emission rates were first documented in 1994; however, anecdotal information and low 14C in post-1989 tree rings suggest that an abrupt increase in both concentrations and emission rates probably began in 1990, following a 6-month period of seismic swarm activity beneath the mountain. Emissions in an area on the south flank of the mountain have been the focus of CO2 monitoring and have shown no indications of abatement between 1994 and 2005, during which estimates of the total CO2 efflux ranged from 90 to 150 MT/d. The variations can be partly attributed to the precision of the techniques and to minor differences in measurement protocols between researchers; variations in soil- moisture and atmospheric conditions alone can cause fluctuations in efflux of ± 10% over periods of hours to days.

Satellite assisted aerosol correlation in a sequestered CO2 leakage controlled site

NASA Astrophysics Data System (ADS)

Landulfo, Eduardo; da Silva Lopes, Fábio J.; Nakaema, Walter M.; de Medeiros, José A. G.; Moreira, Andrea

2014-10-01

Currently one of the main challenges in CO2 storage research is to grant the development, testing and validation of accurate and efficient Measuring, Monitoring and Verification (MMV) techniques to be deployed at the final storage site, targeting maximum storage efficiency at the minimal leakage risk levels. For such task a mimetic sequestration site has been deployed in Florianopolis, Brazil, in order to verify the performance of monitoring plataforms to detect and quantify leakages of ground injected CO2, namely a Cavity Ring Down System (CRDS) - Los Gatos Research - an Eddy Covariance System (Campbell Scientific and Irgason) and meteorological tower for wind, humidity, precipitation and temperature monitoring onsite. The measurement strategy for detecting CO2 leakages can be very challenging since environmental and phytogenic influence can be very severe and play a role on determining if the values measured are unambiguous or not. One external factor to be considered is the amount of incoming solar radiation which will be the driving force for the whole experimental setup and following this reasoning the amount of aerosols in the atmospheric column can be a determinant factor influencing the experimental results. Thus the investigation of measured fluxes CO2 and its concentration with the aforementioned experimental instruments and their correlation with the aerosol data should be taken into account by means of satellite borne systems dedicated to measure aerosol vertical distribution and its optical properties, in this study we have selected CALIPSO and MODIS instrumentation to help on deriving the aerosol properties and CO2 measurements.

The O2-assisted Al/CO2 electrochemical cell: A system for CO2 capture/conversion and electric power generation.

PubMed

Al Sadat, Wajdi I; Archer, Lynden A

2016-07-01

Economical and efficient carbon capture, utilization, and sequestration technologies are a requirement for successful implementation of global action plans to reduce carbon emissions and to mitigate climate change. These technologies are also essential for longer-term use of fossil fuels while reducing the associated carbon footprint. We demonstrate an O2-assisted Al/CO2 electrochemical cell as a new approach to sequester CO2 emissions and, at the same time, to generate substantial amounts of electrical energy. We report on the fundamental principles that guide operations of these cells using multiple intrusive electrochemical and physical analytical methods, including chronopotentiometry, cyclic voltammetry, direct analysis in real-time mass spectrometry, energy-dispersive x-ray spectroscopy, x-ray photoelectron spectroscopy, and coupled thermogravimetric analysis-Fourier transform infrared spectroscopy. On this basis, we demonstrate that an electrochemical cell that uses metallic aluminum as anode and a carbon dioxide/oxygen gas mixture as the active material in the cathode provides a path toward electrochemical generation of a valuable (C2) species and electrical energy. Specifically, we show that the cell first reduces O2 at the cathode to form superoxide intermediates. Chemical reaction of the superoxide with CO2 sequesters the CO2 in the form of aluminum oxalate, Al2(C2O4)3, as the dominant product. On the basis of an analysis of the overall CO2 footprint, which considers emissions associated with the production of the aluminum anode and the CO2 captured/abated by the Al/CO2-O2 electrochemical cell, we conclude that the proposed process offers an important strategy for net reduction of CO2 emissions.

The O2-assisted Al/CO2 electrochemical cell: A system for CO2 capture/conversion and electric power generation

PubMed Central

Al Sadat, Wajdi I.; Archer, Lynden A.

2016-01-01

Economical and efficient carbon capture, utilization, and sequestration technologies are a requirement for successful implementation of global action plans to reduce carbon emissions and to mitigate climate change. These technologies are also essential for longer-term use of fossil fuels while reducing the associated carbon footprint. We demonstrate an O2-assisted Al/CO2 electrochemical cell as a new approach to sequester CO2 emissions and, at the same time, to generate substantial amounts of electrical energy. We report on the fundamental principles that guide operations of these cells using multiple intrusive electrochemical and physical analytical methods, including chronopotentiometry, cyclic voltammetry, direct analysis in real-time mass spectrometry, energy-dispersive x-ray spectroscopy, x-ray photoelectron spectroscopy, and coupled thermogravimetric analysis–Fourier transform infrared spectroscopy. On this basis, we demonstrate that an electrochemical cell that uses metallic aluminum as anode and a carbon dioxide/oxygen gas mixture as the active material in the cathode provides a path toward electrochemical generation of a valuable (C2) species and electrical energy. Specifically, we show that the cell first reduces O2 at the cathode to form superoxide intermediates. Chemical reaction of the superoxide with CO2 sequesters the CO2 in the form of aluminum oxalate, Al2(C2O4)3, as the dominant product. On the basis of an analysis of the overall CO2 footprint, which considers emissions associated with the production of the aluminum anode and the CO2 captured/abated by the Al/CO2-O2 electrochemical cell, we conclude that the proposed process offers an important strategy for net reduction of CO2 emissions. PMID:27453949

Acetone in theGlobal Troposphere: Its Possible Role as a Global Source of PAN

NASA Technical Reports Server (NTRS)

Singh, H. B.; Kanakidou, M.

1994-01-01

Oxygenated hydrocarbons are thought to be important components of the atmosphere but, with the exception of formaldehyde, very little about their distribution and fate is known. Aircraft measurements of acetone (CH3COCH3), PAN (CH3CO3NO2) and other organic species (e. g. acetaldehyde, methanol and ethanol) have been performed over the Pacific, the southern Atlantic, and the subarctic atmospheres. Sampled areas extended from 0 to 12 km altitude over latitudes of 70 deg N to 40 deg S. All measurements are based on real time in-situ analysis of cryogenically preconcentrated air samples. Substantial concentrations of these oxygenated species (10-2000 ppt) have been observed at all altitudes and geographical locations in the troposphere. Important sources include, emissions from biomass burning, plant and vegetation, secondary oxidation of primary non-methane hydrocarbons, and man-made emissions. Direct measurements within smoke plumes have been used to estimate the biomass burning source. Photochemistry studies are used to suggest that acetone could provide a major source of peroxyacetyl radicals in the atmosphere and play an important role in sequestering reactive nitrogen. Model calculations show that acetone photolysis contributes significantly to PAN formation in the middle and upper troposphere.

CCS Site Optimization by Applying a Multi-objective Evolutionary Algorithm to Semi-Analytical Leakage Models

NASA Astrophysics Data System (ADS)

Cody, B. M.; Gonzalez-Nicolas, A.; Bau, D. A.

2011-12-01

Carbon capture and storage (CCS) has been proposed as a method of reducing global carbon dioxide (CO2) emissions. Although CCS has the potential to greatly retard greenhouse gas loading to the atmosphere while cleaner, more sustainable energy solutions are developed, there is a possibility that sequestered CO2 may leak and intrude into and adversely affect groundwater resources. It has been reported [1] that, while CO2 intrusion typically does not directly threaten underground drinking water resources, it may cause secondary effects, such as the mobilization of hazardous inorganic constituents present in aquifer minerals and changes in pH values. These risks must be fully understood and minimized before CCS project implementation. Combined management of project resources and leakage risk is crucial for the implementation of CCS. In this work, we present a method of: (a) minimizing the total CCS cost, the summation of major project costs with the cost associated with CO2 leakage; and (b) maximizing the mass of injected CO2, for a given proposed sequestration site. Optimization decision variables include the number of CO2 injection wells, injection rates, and injection well locations. The capital and operational costs of injection wells are directly related to injection well depth, location, injection flow rate, and injection duration. The cost of leakage is directly related to the mass of CO2 leaked through weak areas, such as abandoned oil wells, in the cap rock layers overlying the injected formation. Additional constraints on fluid overpressure caused by CO2 injection are imposed to maintain predefined effective stress levels that prevent cap rock fracturing. Here, both mass leakage and fluid overpressure are estimated using two semi-analytical models based upon work by [2,3]. A multi-objective evolutionary algorithm coupled with these semi-analytical leakage flow models is used to determine Pareto-optimal trade-off sets giving minimum total cost vs. maximum mass of CO2 sequestered. This heuristic optimization method is chosen because of its robustness in optimizing large-scale, highly non-linear problems. Trade-off curves are developed for multiple fictional sites with the intent of clarifying how variations in domain characteristics (aquifer thickness, aquifer and weak cap rock permeability, the number of weak cap rock areas, and the number of aquifer-cap rock layers) affect Pareto-optimal fronts. Computational benefits of using semi-analytical leakage models are explored and discussed. [1] Birkholzer, J. (2008) "Research Project on CO2 Geological Storage and Groundwater Resources: Water Quality Effects Caused by CO2 Intrusion into Shallow Groundwater" Berkeley (CA): Lawrence Berkeley National Laboratory (US); 2008 Oct. 473 p. Report No.: 510-486-7134. [2] Celia, M.A. and Nordbotten, J.M. (2011) "Field-scale application of a semi-analytical model for estimation of CO2 and brine leakage along old wells" International Journal of Greenhouse Gas Control, 5 (2011), 257-269. [3] Nordbotten, J.M. and Celia, M.A. (2009) "Model for CO2 leakage including multiple geological layers and multiple leaky wells" Environ. Sci. Technol., 43, 743-749.

Geospatial analysis of near-term potential for carbon-negative bioenergy in the United States

PubMed Central

Baik, Ejeong; Turner, Peter A.; Mach, Katharine J.; Field, Christopher B.; Benson, Sally M.

2018-01-01

Bioenergy with carbon capture and storage (BECCS) is a negative-emissions technology that may play a crucial role in climate change mitigation. BECCS relies on the capture and sequestration of carbon dioxide (CO2) following bioenergy production to remove and reliably sequester atmospheric CO2. Previous BECCS deployment assessments have largely overlooked the potential lack of spatial colocation of suitable storage basins and biomass availability, in the absence of long-distance biomass and CO2 transport. These conditions could constrain the near-term technical deployment potential of BECCS due to social and economic barriers that exist for biomass and CO2 transport. This study leverages biomass production data and site-specific injection and storage capacity estimates at high spatial resolution to assess the near-term deployment opportunities for BECCS in the United States. If the total biomass resource available in the United States was mobilized for BECCS, an estimated 370 Mt CO2⋅y−1 of negative emissions could be supplied in 2020. However, the absence of long-distance biomass and CO2 transport, as well as limitations imposed by unsuitable regional storage and injection capacities, collectively decrease the technical potential of negative emissions to 100 Mt CO2⋅y−1. Meeting this technical potential may require large-scale deployment of BECCS technology in more than 1,000 counties, as well as widespread deployment of dedicated energy crops. Specifically, the Illinois basin, Gulf region, and western North Dakota have the greatest potential for near-term BECCS deployment. High-resolution spatial assessment as conducted in this study can inform near-term opportunities that minimize social and economic barriers to BECCS deployment. PMID:29531081

Time-Lapse Seismic Monitoring and Performance Assessment of CO 2 Sequestration in Hydrocarbon Reservoirs

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

Datta-Gupta, Akhil

Carbon dioxide sequestration remains an important and challenging research topic as a potentially viable approach for mitigating the effects of greenhouse gases on global warming (e.g., Chu and Majumdar, 2012; Bryant, 2007; Orr, 2004; Hepple and Benson, 2005; Bachu, 2003; Grimston et al., 2001). While CO 2 can be sequestered in oceanic or terrestrial biomass, the most mature and effective technology currently available is sequestration in geologic formations, especially in known hydrocarbon reservoirs (Barrufet et al., 2010; Hepple and Benson, 2005). However, challenges in the design and implementation of sequestration projects remain, especially over long time scales. One problem ismore » that the tendency for gravity override caused by the low density and viscosity of CO 2. In the presence of subsurface heterogeneity, fractures and faults, there is a significant risk of CO 2 leakage from the sequestration site into overlying rock compared to other liquid wastes (Hesse and Woods, 2010; Ennis-King and Patterson, 2002; Tsang et al., 2002). Furthermore, the CO 2 will likely interact chemically with the rock in which it is stored, so that understanding and predicting its transport behavior during sequestration can be complex and difficult (Mandalaparty et al., 2011; Pruess et al., 2003). Leakage of CO 2 can lead to such problems as acidification of ground water and killing of plant life, in addition to contamination of the atmosphere (Ha-Duong, 2003; Gasda et al., 2004). The development of adequate policies and regulatory systems to govern sequestration therefore requires improved characterization of the media in which CO 2 is stored and the development of advanced methods for detecting and monitoring its flow and transport in the subsurface (Bachu, 2003).« less

Accelerated weathering of limestone for CO2 mitigation: Opportunities for the stone and cement industries

USGS Publications Warehouse

Langer, William H.; San, Juan A.; Rau, Greg H.; Caldeira, Ken

2009-01-01

Large amounts of limestone fines co-produced during the processing of crushed limestone may be useful in the sequestration of carbon dioxide (CO2). Accelerated weathering of limestone (AWL) is proposed as a low-tech method to capture and sequester CO2 from fossil fuel-fired power plants and other point sources such as cement manufacturing. AWL reactants are readily available, inexpensive and environmentally benign. Waste CO2 is hydrated with water to produce carbonic acid. This reacts with and is neutralized by limestone fines, thus converting CO2 gas to dissolved calcium bicarbonate.

The biokarst system and its carbon sinks in response to pH changes: A simulation experiment with microalgae

NASA Astrophysics Data System (ADS)

Xie, Tengxiang; Wu, Yanyou

2017-03-01

This study aims to explore the changes in a microalgal biokarst system as a potential carbon sink system in response to pH changes. The bidirectional isotope labeling method and mass balance calculation were adopted in a simulated biokarst environment with a series of set pH conditions and three microalgal species. Three key processes of the microalgal biokarst system, including calcite dissolution, CaCO3 reprecipitation, and inorganic carbon assimilation by microalgae, were completely quantitatively described. The combined effects of chemical dissolution and species-specific biodissolution caused a decrease in overall dissolution rate when the pH increased from 7 to 9. CaCO3 reprecipitation and the utilization of dissolved inorganic carbon originating from calcite dissolution decreased when the pH increased from 7 to 9. The three processes exhibited different effects in changing the CO2 atmosphere. The amount of photosynthetic carbon sink was larger at high pH values than at low pH values. However, the CO2 sequestration related to the biokarst process (biokarst carbon sink) increased with decreasing pH. Overall, the total amount of sequestered CO2 produced by the biokarst system (CaCO3-CO2-microalgae) shows a minimum at a specific pH then increases with decreasing pH. Therefore, various processes and carbon sinks in the biokarst system are sensitive to pH changes, and biokarst processes play an important negative feedback role in the release of CO2 by acidification. The results also suggest that the carbon sink associated with carbonate weathering cannot be neglected when considering the global carbon cycle on the scale of thousands of years (<3 ka).

Anthropogenic Disturbance of Montane Meadows May Cause Substantial Loss of Soil Carbon to the Atmosphere

NASA Astrophysics Data System (ADS)

Reed, C. C.; Sullivan, B. W.; Hart, S. C.; Drew, M.; Merrill, A.

2016-12-01

High-elevation meadows are biological hotspots that contain high densities of soil carbon (C). The capacity of these ecosystems to sequester C depends on a combination of high primary productivity, seasonally low temperatures, and anaerobic soil conditions associated with water tables at or near the soil surface. However, anthropogenic disturbances in many montane meadows in California's Sierra Nevada have lowered water tables, decreased primary productivity, and created aerobic soil conditions - changes that may alter the balance of greenhouse gas (GHG) emissions and reverse meadows from a net C sink to a net source. Recently, C policy in California has spurred interest in the potential of hydrologic restoration to increase C sequestration in meadows. However, soil C pools and fluxes in degraded meadows must be quantified before the impacts of restoration can accurately be assessed. In this study, we measured soil C stocks in surface soil (1 m) and annual soil GHG fluxes (carbon dioxide (CO2), methane (CH4), and nitrous oxide (N2O)) in three degraded, northern Sierra Nevada meadows. In a parallel laboratory incubation, we manipulated meadow soil water content to determine target goals for restoration of anaerobic conditions. Our results suggest that degraded meadows contain large reservoirs of existing C, but that this C may be vulnerable to decomposition under current conditions. Soil CO2 fluxes ranged from 26.7-33.1 Mg of CO2 ha-1 y-1, roughly equivalent to the amount of C sequestered annually by 70 acres of U.S. forests. These high rates of soil respiration, combined with low primary productivity, resulted in substantial losses of soil C with implications for climate change, ecosystem function, and restoration. Soils from these meadows were a net source of N2O and a net sink of CH4, but these fluxes were 4 orders of magnitude smaller than CO2. Also, we found substantial GHG emissions persist in these organic soils at peak soil moisture, suggesting that restoration may need to sustain soil water holding capacities in excess of 115%, and possibly 200%, for anaerobic soil conditions to return. These findings highlight the need to conserve properly functioning meadows and provide target conditions for optimal restoration of degraded meadows.

Anthropogenic CO2 in a dense water formation area of the Mediterranean Sea

NASA Astrophysics Data System (ADS)

Ingrosso, Gianmarco; Bensi, Manuel; Cardin, Vanessa; Giani, Michele

2017-05-01

There is growing evidence that the on-going ocean acidification of the Mediterranean Sea could be favoured by its active overturning circulation. The areas of dense water formation are, indeed, preferential sites for atmospheric carbon dioxide absorption and through them the ocean acidification process can quickly propagate into the deep layers. In this study we estimated the concentration of anthropogenic CO2 (Cant) in the dense water formation areas of the middle and southern Adriatic Sea. Using the composite tracer TrOCA (Tracer combining Oxygen, inorganic Carbon, and total Alkalinity) and carbonate chemistry data collected throughout March 2013, our results revealed that a massive amount of Cant has invaded all the identified water masses. High Cant concentration was detected at the bottom layer of the Pomo Pit (middle Adriatic, 96.8±9.7 μmol kg-1) and Southern Adriatic Pit (SAP, 85.2±9.4 μmol kg-1), associated respectively with the presence of North Adriatic Dense Water (NAdDW) and Adriatic Dense Water (AdDW). This anthropogenic contamination was clearly linked to the dense water formation events, which govern strong CO2 flux from the atmosphere to the sea and the sinking of dense, CO2-rich surface waters to the deep sea. However, a very high Cant level (94.5±12.5 μmol kg-1) was also estimated at the intermediate layer, as a consequence of a recent vertical mixing that determined the physical and biogeochemical modification of the water of Levantine origin (i.e. Modified Levantine Intermediate Water, MLIW) and favoured the atmospheric CO2 intrusion. The penetration of Cant in the Adriatic Sea determined a significant pH reduction since the pre-industrial era (- 0.139±0.019 pH units on average). This estimation was very similar to the global Mediterranean Sea acidification, but it was again more pronounced at the bottom of the Pomo Pit, within the layer occupied by NAdDW (- 0.157±0.018 pH units), and at the intermediate layer of the recently formed MLIW (- 0.143±0.020 pH units). Our results indicate that the Adriatic Sea could potentially be one of the Mediterranean regions most affected by the ocean acidification and also demonstrate its active role in sequestering and storing Cant.

Proceedings from the second science team meeting of the United States of America Department of Energy and the People's Republic of China Academia Sinica Joint Research Program on CO/sub 2/-Induced Climate Change

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

Not Available

The six papers presented here as the proceedings of this second Joint CO/sub 2/ Research Team Meeting are examples of the research progress during the last two years. The first paper is documentation of the first numerical climate simulation model developed by the Institute of Atmospheric Physics in Beijing. Two papers from the National Oceanic and Atmospheric Administration's National Climatic Data Center at Asheville, North Carolina, demonstrate the work being done on the United States Historical Climatology Network data (the time series of temperature, precipitation, and sunshine) in the US. The fourth paper speaks of climate variability on a regionalmore » scale being much larger than that based on averages of global-wide data and therefore more difficult to predict. The China Precipitation Proxy Index covers a period of 510 years. This permits comparison of contemporary climate patterns (i.e., the last 100 years) with the period of the Little Ice Age when the mean temperature over China was 2/degree/ colder than present. The fifth paper is fascinating documentation of the effects of climate change upon the wild elephants whose habitat has shifted from as far north as Beijing, in historical times, to a currently small, sequestered section in the southwest corner of the country. The final paper demonstrates the pragmatic exchange of both data and technical assistance between the two countries.« less

Mineral Carbonation Employing Ultramafic Mine Waste

NASA Astrophysics Data System (ADS)

Southam, G.; McCutcheon, J.; Power, I. M.; Harrison, A. L.; Wilson, S. A.; Dipple, G. M.

2014-12-01

Carbonate minerals are an important, stable carbon sink being investigated as a strategy to sequester CO2 produced by human activity. A natural playa (Atlin, BC, CAN) that has demonstrated the ability to microbially-accelerate hydromagnesite formation was used as an experimental model. Growth of microbial mats from Atlin, in a 10 m long flow-through bioreactor catalysed hydromagnesite precipitation under 'natural' conditions. To enhance mineral carbonation, chrysotile from the Clinton Creek Asbestos Mine (YT, CAN) was used as a target substrate for sulphuric acid leaching, releasing as much as 94% of the magnesium into solution via chemical weathering. This magnesium-rich 'feedstock' was used to examine the ability of the microbialites to enhance carbonate mineral precipitation using only atmospheric CO2 as the carbon source. The phototrophic consortium catalysed the precipitation of platy hydromagnesite [Mg5(CO3)4(OH)2·4H2O] accompanied by magnesite [MgCO3], aragonite [CaCO3], and minor dypingite [Mg5(CO3)4(OH)2·5H2O]. Scanning Electron Microscopy-Energy Dispersive Spectroscopy indicated that cell exteriors and extracellular polymeric substances (EPS) served as nucleation sites for carbonate precipitation. In many cases, entire cyanobacteria filaments were entombed in magnesium carbonate coatings, which appeared to contain a framework of EPS. Cell coatings were composed of small crystals, which intuitively resulted from rapid crystal nucleation. Excess nutrient addition generated eutrophic conditions in the bioreactor, resulting in the growth of a pellicle that sealed the bioreactor contents from the atmosphere. The resulting anaerobic conditions induced fermentation and subsequent acid generation, which in turn caused a drop in pH to circumneutral values and a reduction in carbonate precipitation. Monitoring of the water chemistry conditions indicated that a high pH (> 9.4), and relatively high concentrations of magnesium (> 3000 ppm), compared with the natural wetland (up to 1000 ppm), and dissolved inorganic carbon (> 20 mM C) were ideal for carbonate precipitation. Under optimum nutrient and magnesium inputs, a mass balance calculation using water chemistry data and hydromagnesite as the sole mineral product resulted in a carbon sequestration rate of 61 t C/ha/year.

Measurement of carbon for carbon sequestration and site monitoring

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

Martin, Madhavi Z; Wullschleger, Stan D; Garten Jr, Charles T

A 2 to 6 degree C increase in global temperature by 2050 has been predicted due to the production of greenhouse gases that is directly linked to human activities. This has encouraged an increase in the international efforts on ways to reduce anthropogenic emissions of greenhouse gases particularly carbon dioxide (CO{sub 2}) as evidence for the link between atmospheric greenhouse gases and climate change has been established. Suggestion that soils and vegetation could be managed to increase their uptake and storage of CO{sub 2}, and thus become 'land carbon sinks' is an incentive for scientists to undertake the ability tomore » measure and quantify the carbon in soils and vegetation to establish base-line quantities present at this time. The verification of the permanence of these carbon sinks has raised some concern regarding the accuracy of their long-term existence. Out of the total percentage of carbon that is potentially sequestered in the terrestrial land mass, only 25% of that is sequestered above ground and almost 75% is hypothesized to be sequestered underground. Soil is composed of solids, liquids, and gases which is similar to a three-phase system. The gross chemical composition of soil organic carbon (SOC) consists of 65% humic substances that are amorphous, dark-colored, complex, polyelectrolyte-like materials that range in molecular weight from a few hundred to several thousand Daltons. The very complex structure of humic and fulvic acid makes it difficult to obtain a spectral signature for all soils in general. The humic acids of different soils have been observed to have polymeric structure, appearing as rings, chains and clusters as seen in electron microscope observations. The humification processes of the soils will decide the sizes of their macromolecules that range from 60-500 angstroms. The percentage of the humus that occurs in the light brown soils is much lower than the humus present in dark brown soils. The humus of forest soils is characterized by a high content of fulvic acids while the humus of peat and grassland soils is high in humic acids. Similarly it is well known that the amount of carbon present in forest soils is lower than the amount present in grassland soils.« less

Terrestrial Carbon Sequestration with Biochar: A Preliminary Assessment of its Global Potential

NASA Astrophysics Data System (ADS)

Amonette, J.; Lehmann, J.; Joseph, S.

2007-12-01

Biochar technology involves the capture of CO2 from the atmosphere by photosynthesis and its ultimate conversion to biochar by pyrolysis. Energy is obtained during the pyrolysis process and the charcoal, or biochar, which is considerably more stable than biomass, may then be incorporated into agricultural lands where it serves to increase the nutrient- and water-holding capacity of soil. With an estimated half-life in soil on the order of centuries to millenia, biochar offers a way of safely storing C for long periods of time while enhancing the productivity of terrestrial ecosystems. Moreover, biochar technology, like other biomass conversion approaches that include C sequestration options, offers a way to decrease the levels of CO2 in the atmosphere. That is, biochar technology is one of the few inherently "carbon-negative" sources of energy. These positive attributes are of little consequence, however, if the total contribution to sequestration is small compared to the need. In this paper, we provide a preliminary assessment of the potential contribution of biochar technology to the mitigation of climate change, and identify some research needs. Currently, the atmospheric C levels are increasing by about 4.1 Gt/yr, with 7.2 Gt/yr being put into the atmosphere by fossil fuel combustion and cement production, and 3.1 Gt/yr being removed from the atmosphere by the ocean (2.2 Gt/yr) and terrestrial processes (0.9 Gt/yr). The uptake by terrestrial processes can be increased significantly by management of the 60.6 Gt/yr of biomass C that is fixed by photosynthesis (i.e., net primary productivity), of which 59 Gt/yr is decomposed and 1.6 Gt/yr combusted. Biomass pyrolysis converts about 50% of the biomass C to char. Of the other 50% that is converted to bio-oil and bio-gas, the net energy production is about 62% efficient. Thus, pyrolysis of 1 Gt of biomass C would provide energy equivalent to about 0.3 Gt of fossil C and could be used to offset that amount of fossil C, while sequestering 0.5 Gt as biochar. Of the 60.6 Gt/yr of biomass that is fixed in usable form, we estimate that perhaps 10% of it (6.1 Gt/yr) could become available in one form or another (crop and forestry residues, and animal waste) for pyrolysis. This level of pyrolysis would offset 1.8 Gt/yr of fossil C, and sequester 3.0 Gt/yr as biochar, enough to halt the increase and actually decrease the level of atmospheric C by 0.7 Gt/yr. Even at half this level (i.e., 5% of annually fixed biomass), pyrolysis would be sufficient to decrease the global C cycle imbalance by 2.4 Gt/yr and in combination with other sequestration options help to achieve the minimum goal of C neutrality. Clearly, the potential contribution of biochar technology is large, perhaps large enough to mitigate climate change alone. However, this preliminary assessment is tempered by several unknowns. Research is needed to further define the impacts of biochar amendments on soil biota, productivity, and greenhouse gas production. For example, there is some evidence that N2O and CH4 production is decreased by biochar amendments, but the mechanisms responsible are unknown. The impact of different types of biochar and pyrolysis conditions also needs to be determined. Lastly, total accounting for greenhouse gas emissions coupled with economic analyses to determine the economic potential of the technology under various scenarios is essential.

A new tool for long-term studies of POM-bacteria interactions: overcoming the century-old Bottle Effect

PubMed Central

Ionescu, Danny; Bizic-Ionescu, Mina; Khalili, Arzhang; Malekmohammadi, Reza; Morad, Mohammad Reza; de Beer, Dirk; Grossart, Hans-Peter

2015-01-01

Downward fluxes of particulate organic matter (POM) are the major process for sequestering atmospheric CO2 into aquatic sediments for thousands of years. Budget calculations of the biological carbon pump are heavily based on the ratio between carbon export (sedimentation) and remineralization (release to the atmosphere). Current methodologies determine microbial dynamics on POM using closed vessels, which are strongly biased towards heterotrophy due to rapidly changing water chemistry (Bottle Effect). We developed a flow-through rolling tank for long term studies that continuously maintains POM at near in-situ conditions. There, bacterial communities resembled in-situ communities and greatly differed from those in the closed systems. The active particle-associated community in the flow-through system was stable for days, contrary to hours previously reported for closed incubations. In contrast to enhanced respiration rates, the decrease in photosynthetic rates on particles throughout the incubation was much slower in our system than in traditional ones. These results call for reevaluating experimentally-derived carbon fluxes estimated using traditional methods. PMID:26435525

Ferric iron-bearing sediments as a mineral trap for CO2 sequestration: Iron reduction using sulfur-bearing waste gas

USGS Publications Warehouse

Palandri, J.L.; Kharaka, Y.K.

2005-01-01

We present a novel method for geologic sequestration of anthropogenic CO2 in ferrous carbonate, using ferric iron present in widespread redbeds and other sediments. Iron can be reduced by SO2 that is commonly a component of flue gas produced by combustion of fossil fuel, or by adding SO2 or H2S derived from other industrial processes to the injected waste gas stream. Equilibrium and kinetically controlled geochemical simulations at 120 bar and 50 and 100 ??C with SO2 or H2S show that iron can be transformed almost entirely to siderite thereby trapping CO2, and simultaneously, that sulfur can be converted predominantly to dissolved sulfate. If there is an insufficient amount of sulfur-bearing gas relative to CO2 as for typical flue gas, then some of the iron is not reduced, and some of the CO2 is not sequestered. If there is an excess of sulfur-bearing gas, then complete iron reduction is ensured, and some of the iron precipitates as pyrite or other solid iron sulfide, depending on their relative precipitation kinetics. Gas mixtures with insufficient sulfur relative to CO2 can be used in sediments containing Ca, Mg, or other divalent metals capable of precipitating carbonate minerals. For quartz arenite with an initial porosity of 21% and containing 0.25 wt.% Fe2O3, approximately 0.7 g of CO2 is sequestered per kg of rock, and the porosity decrease is less than 0.03%. Sequestration of CO2 using ferric iron has the advantage of disposing of SO2 that may already be present in the combustion gas. ?? 2005 Published by Elsevier B.V.

Whole Farm Net Greenhouse Gas Abatement from Establishing Kikuyu-Based Perennial Pastures in South-Western Australia

PubMed Central

Thomas, Dean T.; Sanderman, Jonathan; Eady, Sandra J.; Masters, David G.; Sanford, Paul

2012-01-01

Simple Summary Greenhouse gas (GHG) emissions from ruminant livestock production (sheep, cattle and goats) have contributed to a common perception that a shift in the human diet from animal to plant-based products is environmentally responsible. In this study we found that the level of net emissions from livestock production systems is strongly influenced by the type of farming system that is used, and in fact GHG emission levels from some livestock production systems may be comparable with cropping systems. By introducing into farming systems ‘perennial’ pasture plants that are able to capture more atmospheric carbon, which is then stored in the soil, emission levels from livestock production can be substantially reduced. Abstract On-farm activities that reduce GHG emissions or sequester carbon from the atmosphere to compensate for anthropogenic emissions are currently being evaluated by the Australian Government as carbon offset opportunities. The aim of this study was to examine the implications of establishing and grazing Kikuyu pastures, integrated as part of a mixed Merino sheep and cropping system, as a carbon offset mechanism. For the assessment of changes in net greenhouse gas emissions, results from a combination of whole farm economic and livestock models were used (MIDAS and GrassGro). Net GHG emissions were determined by deducting increased emissions from introducing this practice change (increased methane and nitrous oxide emissions due to higher stocking rates) from the soil carbon sequestered from growing the Kikuyu pasture. Our results indicate that livestock systems using perennial pastures may have substantially lower net GHG emissions, and reduced GHG intensity of production, compared with annual plant-based production systems. Soil carbon accumulation by converting 45% of arable land within a farm enterprise to Kikuyu-based pasture was determined to be 0.80 t CO2-e farm ha−1 yr−1 and increased GHG emissions (leakage) was 0.19 t CO2-e farm ha−1 yr−1. The net benefit of this practice change was 0.61 t CO2-e farm ha−1 yr−1 while the rate of soil carbon accumulation remains constant. The use of perennial pastures improved the efficiency of animal production almost eight fold when expressed as carbon dioxide equivalent emissions per unit of animal product. The strategy of using perennial pasture to improve production levels and store additional carbon in the soil demonstrates how livestock should be considered in farming systems as both sources and sinks for GHG abatement. PMID:26487024

Effects of dissolved CO2 on Shallow Freshwater Microbial Communities simulating a CO2 Leakage Scenario

NASA Astrophysics Data System (ADS)

Gulliver, D. M.; Lowry, G. V.; Gregory, K.

2013-12-01

Geological carbon sequestration is likely to be part of a comprehensive strategy to minimize the atmospheric release of greenhouse gasses, establishing a concern of sequestered CO2 leakage into overlying potable aquifers. Leaking CO2 may affect existing biogeochemical processes and therefore water quality. There is a critical need to understand the evolution of CO2 exposed microbial communities that influence the biogeochemistry in these freshwater aquifers. The evolution of microbial ecology for different CO2 exposure concentrations was investigated using fluid-slurry samples obtained from a shallow freshwater aquifer (55 m depth, 0.5 MPa, 22 °C, Escatawpa, MS). The microbial community of well samples upstream and downstream of CO2 injection was characterized. In addition, batch vessel experiments were conducted with the upstream aquifer samples exposed to varying pCO2 from 0% to 100% under reservoir temperature and pressure for up to 56 days. The microbial community of the in situ experiment and the batch reactor experiment were analyzed with 16S rRNA clone libraries and qPCR. In both the in situ experiment and the batch reactor experiment, DNA concentration did not correlate with CO2 exposure. Both the in situ experiment and the batch reactors displayed a changing microbial community with increased CO2 exposure. The well water isolate, Curvibacter, appeared to be the most tolerant genus to high CO2 concentrations in the in situ experiments and to mid-CO2 concentrations in the batch reactors. In batch reactors with pCO2 concentrations higher than experienced in situ (pCO2 = 0.5 MPa), Pseudomonas appeared to be the most tolerant genus. Findings provide insight into a dynamic biogeochemical system that will alter with CO2 exposure. Adapted microbial populations will eventually give rise to the community that will impact the metal mobility and water quality. Knowledge of the surviving microbial populations will enable improved models for predicting the fate of CO2 following leakage and lead to better strategies for ensuring the quality of potable aquifer water.

Stomatal Conductance, Plant Species Distribution, and an Exploration of Rhizosphere Microbes and Mycorrhizae at a Deliberately Leakimg Experimental Carbon Sequestration Field (ZERT)

NASA Astrophysics Data System (ADS)

Sharma, B.; Apple, M. E.; Morales, S.; Zhou, X.; Holben, B.; Olson, J.; Prince, J.; Dobeck, L.; Cunningham, A. B.; Spangler, L.

2010-12-01

One measure to reduce atmospheric CO2 is to sequester it in deep geological formations. Rapid surface detection of any CO2 leakage is crucial. CO2 leakage rapidly affects vegetation above sequestration fields. Plant responses to high CO2 are valuable tools in surface detection of leaking CO2. The Zero Emission Research Technology (ZERT) site in Bozeman, MT is an experimental field for surface detection of CO2 where 0.15 ton/day of CO2 was released (7/19- 8/15/2010) from a 100m horizontal injection well, HIW, 1.5 m underground with deliberate leaks of CO2 at intervals, and from a vertical injector, VI, (6/3-6/24/2010). The vegetation includes Taraxacum officinale (Dandelion), Dactylis glomerata (Orchard Grass), and other herbaceous plants. We collected soil and roots 1, 3 and 5 m from the VI to determine the responses of mycorrhizal fungi and rhizosphere microbes to high CO2. Mycorrhizal fungi obtain C from root exudates, increase N and P availability, and reduce desiccation, while prokaryotic rhizosphere microbes fix atmospheric N and will be examined for abundance and expression of carbon and nitrogen cycling genes. We are quantifying mycorrhizal colonization and the proportion of spores, hyphae, and arbuscules in vesicular-arbuscular mycorrhizae (VAM) in cleared and stained roots. Stomatal conductance is an important measure of CO2 uptake and water loss via transpiration. We used a porometer (5-40°C, 0-90% RH, Decagon) to measure stomatal conductivity in dandelion and orchard grass at 1, 3, and 5 m from the VI and along a transect perpendicular to the HIW. Dandelion conductance was highest close to the VI and almost consistently higher close to hot spots (circular regions with maximum CO2 and leaf dieback) at the HIW, with 23.2 mmol/m2/s proximal to the hot spot, and 10.8 mmol/m2/s distally. Average conductance in grass (50.3 mmol/m2/s) was higher than in dandelion, but grass did not have high conductance near hot spots. Stomata generally close at elevated CO2. Dandelion leaves near hot spots undergo rapid color change from green to red before senescing to a desiccated brown, while xeromorphic grass leaves do not. Species-specific differences in leaf survival following exposure to CO2 may be linked to species-specific differences in stomatal conductance, and to rhizosphere and mycorrhizal responses. Initial survey results of plant species distribution suggest a shift from a dandelion-grass to a grass-dominated community over hot spots. Sudden and long-term shifts in species composition have important ecological implications and may provide a means of surface detection of upwelling CO2.

Stochastic injection-strategy optimization for the preliminary assessment of candidate geological storage sites

NASA Astrophysics Data System (ADS)

Cody, Brent M.; Baù, Domenico; González-Nicolás, Ana

2015-09-01

Geological carbon sequestration (GCS) has been identified as having the potential to reduce increasing atmospheric concentrations of carbon dioxide (CO2). However, a global impact will only be achieved if GCS is cost-effectively and safely implemented on a massive scale. This work presents a computationally efficient methodology for identifying optimal injection strategies at candidate GCS sites having uncertainty associated with caprock permeability, effective compressibility, and aquifer permeability. A multi-objective evolutionary optimization algorithm is used to heuristically determine non-dominated solutions between the following two competing objectives: (1) maximize mass of CO2 sequestered and (2) minimize project cost. A semi-analytical algorithm is used to estimate CO2 leakage mass rather than a numerical model, enabling the study of GCS sites having vastly different domain characteristics. The stochastic optimization framework presented herein is applied to a feasibility study of GCS in a brine aquifer in the Michigan Basin (MB), USA. Eight optimization test cases are performed to investigate the impact of decision-maker (DM) preferences on Pareto-optimal objective-function values and carbon-injection strategies. This analysis shows that the feasibility of GCS at the MB test site is highly dependent upon the DM's risk-adversity preference and degree of uncertainty associated with caprock integrity. Finally, large gains in computational efficiency achieved using parallel processing and archiving are discussed.

Reducing Energy-Related CO2 Emissions Using Accelerated Limestone Weathering

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

Rau, G H; Knauss, K G; Langer, W H

2004-04-27

Following earlier descriptions, the use and impacts of accelerated weathering of limestone AWL; reaction: CO{sub 2} + H{sub 2}O + CaCO{sub 3} {yields} Ca{sup 2+} + 2(HCO{sub 3}{sup -}) as a CO{sub 2} capture and sequestration method is further explored. Since ready access to the ocean is likely an essential requirement for AWL, it is shown that significant limestone resources are relatively close to a majority of CO{sub 2}-emitting power plants along the coastal US. Furthermore, waste fines, representing more than 20% of current US crushed limestone production (>10{sup 9} tonnes/yr), could be used in many instances as an inexpensivemore » or free source of AWL carbonate. With limestone transportation to coastal sites then as the dominant cost variable, CO{sub 2} sequestration (plus capture) costs of $3-$4/tonne are achievable in certain locations. While there is vastly more limestone and water on earth than that required for AWL to capture and sequester all fossil fuel CO{sub 2} production, the transportation cost of bringing limestone, seawater, and waste CO{sub 2} into contact likely limits the method's applicability to perhaps 10-20% of US point-source emissions. Using a bench-scale laboratory reactor, it is shown that CO{sub 2} sequestration rates of 10{sup -6} to 10{sup -5} moles/sec per m{sup 2} of limestone surface area are readily achievable using seawater. This translates into reaction densities as high as 2 x 10{sup -2} tonnes CO{sub 2} m{sup -3}day{sup -1}, highly dependent on limestone particle size, solution turbulence and flow, and CO{sub 2} concentration. Modeling of AWL end-solution disposal in the ocean shows significantly reduced effects on ocean pH and carbonate chemistry relative to those caused by direct CO{sub 2} disposal into the atmosphere or ocean. In fact the increase in ocean Ca{sup 2+} and bicarbonate offered by AWL should significantly enhance the growth of corals and other marine calcifiers whose health is currently being threatened by anthropogenic CO{sub 2} invasion and pH reduction in the ocean.« less

The evolution of organic matter along the lower Amazon River continuum - Óbidos to the ocean

NASA Astrophysics Data System (ADS)

Ward, N. D.; Keil, R. G.; Medeiros, P. M.; Brito, D.; Cunha, A.; Sawakuchi, H. O.; Moura, J. S.; Yager, P. L.; Krusche, A. V.; Richey, J. E.

2013-12-01

The influence of the Amazon River on global hydrologic and biogeochemical cycling is well recognized. The Amazon River provides roughly 16% of the global freshwater supply to the ocean and is a significant source of CO2 to the atmosphere, outgassing 0.5 Pg C y-1 to the atmosphere--a flux roughly equivalent to the amount of carbon 'sequestered' by the Amazon rainforest (Field et al, 1998; Richey et al., 2002; Malhi et al., 2008). However, much of our understanding of the flux of matter from the Amazon River into the Atlantic Ocean (and atmosphere) is limited to measurements made at and upstream of Óbidos, 900 km upstream from the actual river mouth. Further, there are few to no observations documenting the transformation of organic matter in a parcel of water as it travels downstream of Óbidos into the ocean. Here we explore the hydrological and biogeochemical evolution of the lower Amazon River continuum, from Óbidos to the Atlantic Ocean. A suite of dissolved and particulate organic matter (OM) parameters were measured during a series of five river expeditions with stations at Óbidos, the Tapajós tributary, the mouth of the Lago Grande de Curuai floodplain lake, both the north and south channels of the Amazon River mouth near Macapá, and the confluence of the Amazon and Tocantins Rivers near Belém. In addition to bulk carbon isotopic signatures, a suite of biomarkers including dissolved and particulate lignin-derived phenols were measured to trace the sources and degradation history of terrestrial vascular plant derived OM throughout the continuum. Dissolved and particulate lignin phenol concentrations both correlated positively with river discharge in the Amazon River mainstem, with variable export patterns from the tributaries and floodplains. As organic matter travels along the continuum it is degraded by microbial composition, fuelling gross respiration and CO2 outgassing. The flux of organic carbon to the ocean is chemically recalcitrant as a result of the constant biological processing of labile OM throughout the lower river. We estimate that 40% of the vascular plant-derived organic carbon sequestered by the terrestrial biosphere is degraded within soils, 55% is degraded along the river continuum, and less than 5% is delivered to the ocean (Ward et al., 2013) References Cited Field, C., M. Behrenfeld, J. Randerson, and P. Falkowski. 1998. Primary production of the biosphere: Integrating terrestrial and oceanic components. Science 281, 237-240. Malhi, Y., Roberts, J.T., Betts, R.A., Killeen, T.J., Li, W., Nobre, C.A. 2008. Climate change, deforestation, and the fate of the Amazon. Science 319, 169-172. Richey, J. E., Melack, J. M., Aufdenkampe, A. K., Ballester, V. M. & Hess, L. L. 2002. Outgassing from Amazonian rivers and wetlands as a large tropical source of atmospheric CO2. Nature 416, 617-620. Ward, N.D.; Keil, R.G.; Medeiros, P.M.; Brito, D.C.; Cunha, A.C.; Dittmar, T.; Yager, P.L.; Krusche, A.V.; Richey, J.E. 2013. Degradation of terrestrially derived macromolecules in the Amazon River. Nature Geoscience. doi: 10.1038/ngeo1817

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

Mohaghegh, Shahab D.

apability of underground carbon dioxide storage to confine and sustain injected CO2 for a very long time is the main concern for geologic CO2 sequestration. If a leakage from a geological CO2 sequestration site occurs, it is crucial to find the approximate amount and the location of the leak in order to implement proper remediation activity. An overwhelming majority of research and development for storage site monitoring has been concentrated on atmospheric, surface or near surface monitoring of the sequestered CO2. This study aims to monitor the integrity of CO2 storage at the reservoir level. This work proposes developing in-situmore » CO2 Monitoring and Verification technology based on the implementation of Permanent Down-hole Gauges (PDG) or “Smart Wells” along with Artificial Intelligence and Data Mining (AI&DM). The technology attempts to identify the characteristics of the CO2 leakage by de-convolving the pressure signals collected from Permanent Down-hole Gauges (PDG). Citronelle field, a saline aquifer reservoir, located in the U.S. was considered for this study. A reservoir simulation model for CO2 sequestration in the Citronelle field was developed and history matched. The presence of the PDGs were considered in the reservoir model at the injection well and an observation well. High frequency pressure data from sensors were collected based on different synthetic CO2 leakage scenarios in the model. Due to complexity of the pressure signal behaviors, a Machine Learning-based technology was introduced to build an Intelligent Leakage Detection System (ILDS). The ILDS was able to detect leakage characteristics in a short period of time (less than a day) demonstrating the capability of the system in quantifying leakage characteristics subject to complex rate behaviors. The performance of ILDS was examined under different conditions such as multiple well leakages, cap rock leakage, availability of an additional monitoring well, presence of pressure drift and noise in the pressure sensor and uncertainty in the reservoir model.« less

Are Salps A Silver Bullet Against Global Warming And Ocean Acidification?

NASA Astrophysics Data System (ADS)

Kithil, P. W.

2006-12-01

Oceanic uptake of 25 billion tons CO2 annually introduced into the atmosphere from carbon fuels must be mitigated to prevent further widespread changes in ocean biochemistry and potentially severe anthropogenic climate change. Larry Madin of Woods Hole Oceanographic Institute and his colleagues have measured the carbon sequestration in the excretia produced by dense swarms of Salps of up to 4,000 tons per day over a 100,000 km2 ocean region, equivalent to over 14 thousand tons of CO2 per day. This poses several questions: 1. Given the ocean surface of 372 million km2, does the Madin report imply a potential removal of 20 billion tons of CO2 per year 80% of emissions? 2. What might be the natural limitations on widespread propagation of Salps, and how would these effect the carbon sequestration actually achieved? 3. What mechanism could encourage the propagation of Salps throughout the oceans? Since Salps feast on phytoplankton which require sunlight and sufficient nutrients, we must first reduce the available ocean by perhaps 60% as a seasonal limit on phytoplankton growth and allow 60% further limit for poor nutrient availability and assuming some ocean regions are an unfavorable environment for Salps. Combined, the net ocean area over which Salps could sequester carbon is thus 36%, or 134 million km2. Assuming Madin's values for carbon sequestration are achievable over this ocean region, about 7.2 billion tons of CO2 could be sequestered annually, equal to 29% of mankind's current fossil-fuel CO2 output. This converts to a carbon equivalent of 1.96 billion tons per year. The mechanism we propose to encourage widespread propagation of Salps is forced upwelling using Atmocean's arrays of wave-driven deep ocean pumps to bring up large volumes of cold, nutrient-rich deep ocean to enhance the ocean's primary production, absorbing CO2 and producing oxygen. The pump simply comprises a buoy, flexible tube, cylinder with valve, cable to connect the buoy and cylinder, and solar panel to power communications & provide remote control. Adjacent pumps are connected at the bottom to maintain relative position. If required, periodic seafloor anchoring can maintain absolute position within an ocean basin. Deployment is low cost as the pumps self-deploy when dropped into the ocean from barges. Pumps would not be deployed in ocean shipping channels, regions used by recreational boaters, nor where excessive tides or currents exist. In a global application, 1,340 arrays each 100,000 km2 are needed to cover the 134 million km2 calculated above. Assuming one pump per square km costing 2,000, an investment of 268 billion is needed. Using a five year payback, this investment is recouped if the carbon credit price is 26.80 per ton applied to sequestering 1.96 billion tons per year of carbon. This is not dramatically different from today's carbon credit price of about 15 per ton. Assuming a governmental mandate of carbon sequestration, today's price could easily increase many-fold, making ocean sequestration using forced upwelling economically attractive. Additional benefits of widespread forced upwelling include: 1 Buffering of ocean pH by removing CO2 during photosynthesis; 2 Possible cooling the upper mixed layer upstream from coral reefs to reduce bleaching from ocean hotspots; 3 Possible mitigation of rapid climate change by enhancing the mixing of arctic/Greenland meltwater; 4 Enhancement of wild fish populations; and, 5 Reduced hurricane intensity, achieved by cooling the upper mixed layer upon approach of a tropical storm in high risk regions such as the Gulf of Mexico.

Method of detecting leakage from geologic formations used to sequester CO.sub.2

DOEpatents

White, Curt [Pittsburgh, PA; Wells, Arthur [Bridgeville, PA; Diehl, J Rodney [Pittsburgh, PA; Strazisar, Brian [Venetia, PA

2010-04-27

The invention provides methods for the measurement of carbon dioxide leakage from sequestration reservoirs. Tracer moieties are injected along with carbon dioxide into geological formations. Leakage is monitored by gas chromatographic analyses of absorbents. The invention also provides a process for the early leak detection of possible carbon dioxide leakage from sequestration reservoirs by measuring methane (CH.sub.4), ethane (C.sub.2H.sub.6), propane (C.sub.3H.sub.8), and/or radon (Rn) leakage rates from the reservoirs. The invention further provides a method for branding sequestered carbon dioxide using perfluorcarbon tracers (PFTs) to show ownership.

Consequences of carbon offset payments for the global forest sector

Treesearch

Joseph Buongiorno; Shushuai. Zhu

2013-01-01

Long-term effects of policies to induce carbon storage in forests were projected with the Global Forest Products Model. Offset pay- ments for carbon sequestered in forest biomass of $15–$50/t CO2 e applied in all countries increased CO2 sequestration in world forests by 5–14 billion tons from 2009 to 2030. Limiting implementation to developed countries exported...

Comments on Economides and Ehlig-Economides,"Sequestering carbon dioxide in a closed underground volume," SPE 124430, October 2009

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

Oldenburg, Curt; Pruess, Karsten; Birkholzer, Jens

The paper examines the pressure increase resulting from injection of CO2 into a 1D radial system with closed boundaries. The finding is that unacceptably high pressures are obtained when only 1% or less of the pore volume is occupied by injected CO2. These results are used to make the general conclusion that large-scale CCS is not feasible.

Component greenhouse gas fluxes and radiative balance from two deltaic marshes in Louisiana: Pairing chamber techniques and eddy covariance

USGS Publications Warehouse

Krauss, Ken W.; Holm, Guerry O.; Perez, Brian C.; McWhorter, David E.; Cormier, Nicole; Moss, Rebecca; Johnson, Darren; Neubauer, Scott C; Raynie, Richard C

2016-01-01

Coastal marshes take up atmospheric CO2 while emitting CO2, CH4, and N2O. This ability to sequester carbon (C) is much greater for wetlands on a per-area basis than from most ecosystems, facilitating scientific, political, and economic interest in their value as greenhouse gas sinks. However, the greenhouse gas balance of Gulf of Mexico wetlands is particularly understudied. We describe the net ecosystem exchange (NEEc) of CO2 and CH4 using eddy covariance (EC) in comparison with fluxes of CO2, CH4, and N2O using chambers from brackish and freshwater marshes in Louisiana, USA. From EC, we found that 182 g C m-2 y-1 was lost through NEEc from the brackish marsh. Of this, 11 g C m-2 y-1 resulted from net CH4 emissions and the remaining 171 g C m-2 y-1 resulted from net CO2 emissions. In contrast, -290 g C m2 y-1 was taken up through NEEc by the freshwater marsh, with 47 g C m-2 y-1 emitted as CH4 and -337 g C m-2 y-1 taken up as CO2. From chambers, we discovered that neither site had large fluxes of N2O. Sustained-flux greenhouse gas accounting metrics indicated that both marshes had a positive (warming) radiative balance, with the brackish marsh having a substantially greater warming effect than the freshwater marsh. That net respiratory emissions of CO2 and CH4 as estimated through chamber techniques were 2-4 times different from emissions estimated through EC requires additional understanding of the artifacts created by different spatial and temporal sampling footprints between techniques.

Federal land management, carbon sequestration, and climate change in the Southeastern U.S.: a case study with fort benning

USGS Publications Warehouse

Zhao, S.; Liu, S.; Li, Z.; Sohl, Terry L.

2010-01-01

Land use activities can have a major impact on the temporal trendsandspatialpatternsofregionalland-atmosphereexchange of carbon. Federal lands generally have substantially different land management strategies from surrounding areas, and the carbon consequences have rarely been quantified and assessed. Using the Fort Benning Installation as a case study, we used the General Ensemble biogeochemical Modeling System (GEMS) to simulate and compare ecosystem carbon sequestration between the U.S. Army's Fort Benning and surrounding areas from 1992 to 2050. Our results indicate that the military installation sequestered more carbon than surrounding areas from 1992 to 2007 (76.7 vs 18.5 g C m-2 yr-1), and is projected to continue sequestering more carbon from 2008 to 2050 (75.7 vs 25.6 g C m-2 yr-1), mostly because of the proactive management approaches adopted on military training lands. Our results suggest that federal lands might play a positive and important role in sequestering and conserving atmospheric carbon because some anthropogenic disturbances (e.g., urbanization, forest harvesting, and agriculture) can be minimized or prevented on federal lands

Geological Sequestration of CO2 by Hydrous Carbonate Formation with Reclaimed Slag

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

Von L. Richards; Kent Peaslee; Jeffrey Smith

The concept of this project is to develop a process that improves the kinetics of the hydrous carbonate formation reaction enabling steelmakers to directly remove CO2 from their furnace exhaust gas. It is proposed to bring the furnace exhaust stream containing CO2 in contact with reclaimed steelmaking slag in a reactor that has an environment near the unit activity of water resulting in the production of carbonates. The CO2 emissions from the plant would be reduced by the amount sequestered in the formation of carbonates. The main raw materials for the process are furnace exhaust gases and specially prepared slag.

A SEA FLOOR GRAVITY SURVEY OF THE SLEIPNER FIELD TO MONITOR CO2 MIGATION

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

Mark Zumberge

2003-06-13

At the Sleipner gas field, excess CO{sub 2} is sequestered and injected underground into a porous saline aquifer 1000 m below the seafloor. A high precision micro-gravity survey was carried out on the seafloor to monitor the injected CO{sub 2}. A repeatability of 5 {micro}Gal in the station averages was observed. This is considerably better than pre-survey expectations. These data will serve as the baseline for time-lapse gravity monitoring of the Sleipner CO{sub 2} injection site. Simple modeling of the first year data give inconclusive results, thus a more detailed approach is needed. Work towards this is underway.

Greenhouse gas emissions and carbon sequestration by agroforestry systems in southeastern Brazil.

PubMed

Torres, Carlos Moreira Miquelino Eleto; Jacovine, Laércio Antônio Gonçalves; Nolasco de Olivera Neto, Sílvio; Fraisse, Clyde William; Soares, Carlos Pedro Boechat; de Castro Neto, Fernando; Ferreira, Lino Roberto; Zanuncio, José Cola; Lemes, Pedro Guilherme

2017-12-01

Agrosilvopastoral and silvopastoral systems can increase carbon sequestration, offset greenhouse gas (GHG) emissions and reduce the carbon footprint generated by animal production. The objective of this study was to estimate GHG emissions, the tree and grass aboveground biomass production and carbon storage in different agrosilvopastoral and silvopastoral systems in southeastern Brazil. The number of trees required to offset these emissions were also estimated. The GHG emissions were calculated based on pre-farm (e.g. agrochemical production, storage, and transportation), and on-farm activities (e.g. fertilization and machinery operation). Aboveground tree grass biomass and carbon storage in all systems was estimated with allometric equations. GHG emissions from the agroforestry systems ranged from 2.81 to 7.98 t CO 2 e ha -1 . Carbon storage in the aboveground trees and grass biomass were 54.6, 11.4, 25.7 and 5.9 t C ha -1 , and 3.3, 3.6, 3.8 and 3.3 t C ha -1 for systems 1, 2, 3 and 4, respectively. The number of trees necessary to offset the emissions ranged from 17 to 44 trees ha -1 , which was lower than the total planted in the systems. Agroforestry systems sequester CO 2 from the atmosphere and can help the GHG emission-reduction policy of the Brazilian government.

Iron fertilisation and century-scale effects of open ocean dissolution of olivine in a simulated CO2 removal experiment

NASA Astrophysics Data System (ADS)

Hauck, Judith; Köhler, Peter; Wolf-Gladrow, Dieter; Völker, Christoph

2016-02-01

Carbon dioxide removal (CDR) approaches are efforts to reduce the atmospheric CO2 concentration. Here we use a marine carbon cycle model to investigate the effects of one CDR technique: the open ocean dissolution of the iron-containing mineral olivine. We analyse the maximum CDR potential of an annual dissolution of 3 Pg olivine during the 21st century and focus on the role of the micro-nutrient iron for the biological carbon pump. Distributing the products of olivine dissolution (bicarbonate, silicic acid, iron) uniformly in the global surface ocean has a maximum CDR potential of 0.57 gC/g-olivine mainly due to the alkalinisation of the ocean, with a significant contribution from the fertilisation of phytoplankton with silicic acid and iron. The part of the CDR caused by ocean fertilisation is not permanent, while the CO2 sequestered by alkalinisation would be stored in the ocean as long as alkalinity is not removed from the system. For high CO2 emission scenarios the CDR potential due to the alkalinity input becomes more efficient over time with increasing ocean acidification. The alkalinity-induced CDR potential scales linearly with the amount of olivine, while the iron-induced CDR saturates at 113 PgC per century (on average ˜ 1.1 PgC yr-1) for an iron input rate of 2.3 Tg Fe yr-1 (1% of the iron contained in 3 Pg olivine). The additional iron-related CO2 uptake occurs in the Southern Ocean and in the iron-limited regions of the Pacific. Effects of this approach on surface ocean pH are small (\\lt 0.01).

Performance of an electrochemical carbon monoxide monitor in the presence of anesthetic gases.

PubMed

Dunning, M; Woehlck, H J

1997-11-01

The passage of volatile anesthetic agents through accidentally dried CO2 absorbents in anesthesia circuits can result in the chemical breakdown of anesthetics with production of greater than 10000 ppm carbon monoxide (CO). This study was designed to evaluate a portable CO monitor in the presence of volatile anesthetic agents. Two portable CO monitors employing electrochemical sensors were tested to determine the effects of anesthetic agents, gas sample flow rates, and high CO concentrations on their electrochemical sensor. The portable CO monitors were exposed to gas mixtures of 0 to 500 ppm CO in either 70% nitrous oxide, 1 MAC concentrations of contemporary volatile anesthetics, or reacted isoflurane or desflurane (containing CO and CHF3) in oxygen. The CO measurements from the electrochemical sensors were compared to simultaneously obtained samples measured by gas chromatography (GC). Data were analyzed by linear regression. Overall correlation between the portable CO monitors and the GC resulted in an r2 value >0.98 for all anesthetic agents. Sequestered samples produced an exponential decay of measured CO with time, whereas stable measurements were maintained during continuous flow across the sensor. Increasing flow rates resulted in higher CO readings. Exposing the CO sensor to 3000 and 19000 ppm CO resulted in maximum reported concentrations of approximately 1250 ppm, with a prolonged recovery. Decrease in measured concentration of the sequestered samples suggests destruction of the sample by the sensor, whereas a diffusion limitation is suggested by the dependency of measured value upon flow. Any value over 500 ppm must be assumed to represent dangerous concentrations of CO because of the non-linear response of these monitors at very high CO concentrations. These portable electrochemical CO monitors are adequate to measure CO concentrations up to 500 ppm in the presence of typical clinical concentrations of anesthetics.

Decay of cacti and carbon cycling

NASA Astrophysics Data System (ADS)

Garvie, Laurence A. J.

2006-03-01

Cacti contain large quantities of Ca-oxalate biominerals, with C derived from atmospheric CO2. Their death releases these biominerals into the environment, which subsequently transform to calcite via a monohydrocalcite intermediate. Here, the fate of Ca-oxalates released by plants in arid environments is investigated. This novel and widespread form of biomineralization has unexpected consequences on C cycling and calcite accumulation in areas with large numbers of cacti. The magnitude of this mineralization is revealed by studying the large columnar cactus Carnegiea gigantea (Engelm.) Britton and Rose in southwestern Arizona (locally called the saguaro). A large C. gigantea contains on the order of 1×105 g of the Ca-oxalate weddellite—CaC2O4·2H2O. In areas with high C. gigantea density, there is an estimated 40 g Catm m-2 sequestered in Ca-oxalates. Following the death of the plant, the weddellite transforms to calcite on the order to 10-20 years. In areas with high saguaro density, there is an estimated release of up to 2.4 g calcite m-2 year-1 onto the desert soil. Similar transformation mechanisms occur with the Ca-oxalates that are abundant in the majority of cacti. Thus, the total atmospheric C returned to the soil of areas with a high number density of cacti is large, suggesting that there may be a significant long-term accumulation of atmospheric C in these soils derived from Ca-oxalate biominerals. These findings demonstrate that plant decay in arid environments may have locally significant impacts on the Ca and inorganic C cycles.

Decay of cacti and carbon cycling.

PubMed

Garvie, Laurence A J

2006-03-01

Cacti contain large quantities of Ca-oxalate biominerals, with C derived from atmospheric CO(2). Their death releases these biominerals into the environment, which subsequently transform to calcite via a monohydrocalcite intermediate. Here, the fate of Ca-oxalates released by plants in arid environments is investigated. This novel and widespread form of biomineralization has unexpected consequences on C cycling and calcite accumulation in areas with large numbers of cacti. The magnitude of this mineralization is revealed by studying the large columnar cactus Carnegiea gigantea (Engelm.) Britton and Rose in southwestern Arizona (locally called the saguaro). A large C. gigantea contains on the order of 1 x 10(5) g of the Ca-oxalate weddellite-CaC(2)O(4) x 2H(2)O. In areas with high C. gigantea density, there is an estimated 40 g C(atm) m(-2) sequestered in Ca-oxalates. Following the death of the plant, the weddellite transforms to calcite on the order to 10-20 years. In areas with high saguaro density, there is an estimated release of up to 2.4 g calcite m(-2) year(-1) onto the desert soil. Similar transformation mechanisms occur with the Ca-oxalates that are abundant in the majority of cacti. Thus, the total atmospheric C returned to the soil of areas with a high number density of cacti is large, suggesting that there may be a significant long-term accumulation of atmospheric C in these soils derived from Ca-oxalate biominerals. These findings demonstrate that plant decay in arid environments may have locally significant impacts on the Ca and inorganic C cycles.

Carbon Dynamics in Isolated Wetlands of the Northern Everglades Watershed is Revealed using Hydrogeophysical Methods and Aerial Imagery

NASA Astrophysics Data System (ADS)

McClellan, M. D.; Job, M. J.; Comas, X.

2016-12-01

Peatlands play a critical role in the carbon (C) cycle by sequestering and storing a large fraction of the global soil C pool; and by producing and releasing significant amounts of greenhouse gasses (CO2, CH4) into the atmosphere. While most studies exploring these attributes have traditionally focused on boreal and subarctic biomes, wetlands in temperate and tropical climates (such as the Florida Everglades) have been understudied despite accounting for more than 20% of the global peatland C stock. We used a combination of indirect non-invasive geophysical methods (ground penetrating radar, GPR), aerial imagery, and direct measurements (gas traps) to estimate the contribution of subtropical isolated wetlands to the total C pool of the pine flatwoods landscape at the Disney Wilderness Preserve (DWP, Poinciana, FL). Measurements were collected within two types of isolated wetlands at the preserve, emergent and forested. Geophysical surveys were collected weekly to 1) define total peat thickness (i.e. from the surface to the mineral soil interface) and 2) estimate changes within the internal gas regime. Direct measurements of gas fluxes using gas traps and time-lapse cameras were used to estimate gas emissions (i.e. CH­4 and CO2). Aerial photographs were used to estimate surface area for each isolated wetland and develop a relationship between surface area and total wetland C production that is then applied to every isolated wetland in the preserve to estimate the total wetland C contribution. This work seeks to provide evidence that isolated wetlands within the central Florida landscape are key contributors of C to the atmosphere.

Atmospheric carbon reduction by urban trees

Treesearch

David J. Nowak

1993-01-01

Trees, because they sequester atmospheric carbon through their growth process and conserve energy in urban areas, have been suggested as one means to combat increasing levels of atmospheric carbon. Analysis of the urban forest in Oakland, California (21% tree cover), reveals a tree carbon storage level of 11.0 metric tons/hectare. Trees in the area of the 1991 fire in...

Assessing the biogeochemical impact of AMOC collapse during Heinrich Stadial 1: New surface and mid-depth records from the South Atlantic

NASA Astrophysics Data System (ADS)

Lund, D. C.; Lacerra, M.; Schmittner, A.; Yu, J.

2017-12-01

Carbon isotope minima were a ubiquitous feature in the mid-depth (1.5-2.5 km) Atlantic during Heinrich Stadial 1 (HS1, 14.5-17.5 kyr BP), with the most likely driver being a collapse of the Atlantic Meridional Overturning Circulation (AMOC) [1, 2]. Model simulations suggest a weaker AMOC increases the residence time of deep water and causes accumulation of isotopically light respired carbon at mid-depths [3]. Subsequent weakening of the biological pump also causes light carbon to accumulate in the surface ocean and atmosphere, potentially accounting for surface ocean δ13C minima and the initial rise in atmospheric CO2. Here, we test the AMOC hypothesis using high resolution planktonic and benthic δ13C records from the Brazil Margin (1.8 km and 2.1 km water depth). We show that N. dutertrei and G. sacculifer δ13C lags benthic δ13C during HS1 by 500 years. Because the planktonic and benthic results are based on analyses of the same samples, the relative timing is constrained by the stratigraphic offset of the δ13C time series. Our results are consistent with the model prediction of an initial collapse of the AMOC causing δ13C minima at mid-depth followed by weakening of the biological pump and equilibration of the surface ocean with a 13C-depleted atmosphere. We also assess ΣCO2 storage in the mid-depth Atlantic during HS1 using benthic foraminiferal B/Ca as a proxy for [CO32-]. Using replicated high resolution B/Ca records, we show that [CO32-] decreased during HS1, synchronous with apparent weakening of the AMOC. The [CO32-] response is smaller than in the tropical North Atlantic [4], indicating there was a north-south gradient in the [CO32-] signal similar to that for δ13C [5]. The implied ΣCO2 signal is consistent with model results [3], suggesting that carbon is temporarily sequestered in the mid-depth Atlantic during millennial-scale stadial events. We estimate that approximately 75% of the mid-depth δ13C signal was driven by accumulation of remineralized carbon, highlighting the non-conservative nature of δ13C during the last deglaciation. 1 McManus, J. et al. (2004) Nature, 428, 834. 2 Oppo, D. et al. (2015) Paleoceanography, 30, 353. 3 Schmittner, A., & Lund, D. (2015) Clim. Past, 11, 135. 4 Yu, J. et al. (2010) Science, 330 (6007), 1084. 5 Lund, D., et al. (2015) Paleoceanography, 30, 477.

Geoengineering the Climate: Approaches to Counterbalancing Global Warming

NASA Astrophysics Data System (ADS)

MacCracken, M. C.

2005-12-01

For the past two hundred years, the inadvertent release of carbon dioxide and other radiatively active gases and aerosols, particularly as a result of combustion of fossil fuels and changes in land cover, have been contributing to global climate change. Global warming to date is approaching 1°C, and this is being accompanied by reduced sea ice, rising sea level, shifting ecosystems and more. Rather than sharply curtailing use of fossil fuels in order to reduce CO2 emissions and eventually eliminate the net human influence on global climate, a number of approaches have been suggested that are intended to advertently modify the climate in a manner to counter-balance the warming influence of greenhouse gas emissions. One general type of approach is carbon sequestration, which focuses on capturing the CO2 and then sequestering it underground or in the ocean. This can be done at the source of emission, by pulling the CO2 out of the atmosphere through some chemical process, or by enhancing the natural processes that remove CO2 from the atmosphere, for example by fertilizing the oceans with iron. A second general approach to geoengineering the climate is to lower the warming influence of the incoming solar radiation by an amount equivalent to the energy captured by the CO2-induced enhancement of the greenhouse effect. Proposals have been made to do this by locating a deflector at the Earth-Sun Lagrange point, lofting many thousands of near-Earth mirrors, injecting aerosols into the stratosphere, or by increasing the surface albedo. A third general approach is to alter natural Earth system processes in ways that would counterbalance the effects of the warming. Among suggested approaches are constructing dams to block various ocean passages, oceanic films to limit evaporation and water vapor feedback, and even, at small scale, to insulate mountain glaciers to prevent melting. Each of these approaches has its advantages, ranging from simplicity to reversibility, and disadvantages, ranging from costs for implementation to associated inadvertent negative environmental consequences. Unless implemented as only a bridging effort, geoengineering would require diversion of substantial, and even growing, resources from the effort to move away from reliance on fossil fuels. Because the lifetime of the excess CO2 in the atmosphere is so long, such efforts would generally need to be maintained for centuries by future generations to avoid a relatively rapid increase in global average temperature, even after emissions of CO2 had eventually been halted. In that such approaches are also fraught with uncertainties, there has been very little study of the details of how such approaches might be pursued and of their overall advertent and inadvertent consequences, leaving the area open to ongoing consideration of sometimes rather speculative possibilities.

Northern California CO 2 Reduction Project

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

Hymes, Edward

2010-06-16

C6 Resources LLC, a wholly owned subsidiary of Shell Oil Company, worked with the US Department of Energy (DOE) under a Cooperative Agreement to develop the Northern California CO 2 Reduction Project. The objective of the Project is to demonstrate the viability of using Carbon Capture and Sequestration (CCS) to reduce existing greenhouse gas emissions from industrial sources on a large-scale. The Project will capture more than 700,000 metric tonnes of CO 2 per year, which is currently being vented to the atmosphere from the Shell Martinez Refinery in Contra Costa County. The CO 2 will be compressed and dehydratedmore » at the refinery and then transported via pipeline to a sequestration site in a rural area in neighboring Solano County. The CO 2 will be sequestered into a deep saline formation (more than two miles underground) and will be monitored to assure secure, long-term containment. The pipeline will be designed to carry as much as 1,400,000 metric tonnes of CO 2 per year, so additional capacity will be available to accommodate CO 2 captured from other industrial sources. The Project is expected to begin operation in 2015. The Project has two distinct phases. The overall objective of Phase 1 was to develop a fully definitive design basis for the Project. The Cooperative Agreement with the DOE provided cost sharing for Phase 1 and the opportunity to apply for additional DOE cost sharing for Phase 2, comprising the design, construction and operation of the Project. Phase 1 has been completed. DOE co-funding is provided by the American Recovery and Reinvestment Act (ARRA) of 2009. As prescribed by ARRA, the Project will stimulate the local economy by creating manufacturing, transportation, construction, operations, and management jobs while addressing the need to reduce greenhouse gas emissions at an accelerated pace. The Project, which will also assist in meeting the CO 2 reduction requirements set forth in California's Climate Change law, presents a major opportunity for both the environment as well as the region. C6 Resources is conducting the Project in collaboration with federally-funded research centers, such as Lawrence Berkeley National Lab and Lawrence Livermore National Lab. C6 Resources and Shell have identified CCS as one of the critical pathways toward a worldwide goal of providing cleaner energy. C6 Resources, in conjunction with the West Coast Regional Carbon Sequestration Partnership (WESTCARB), has conducted an extensive and ongoing public outreach and CCS education program for local, regional and state-wide stakeholders. As part of a long term relationship, C6 Resources will continue to engage directly with community leaders and residents to ensure public input and transparency. This topical report summarizes the technical work from Phase 1 of the Project in the following areas; Surface Facility Preliminary Engineering: summarizes the preliminary engineering work performed for CO 2 capture, CO 2 compression and dehydration at the refinery, and surface facilities at the sequestration site; Pipeline Preliminary Engineering: summarizes the pipeline routing study and preliminary engineering design; Geologic Sequestration: summarizes the work to characterize, model and evaluate the sequestration site; and Monitoring, Verification and Accounting (MVA): summarizes the MVA plan to assure long-term containment of the sequestered CO 2.« less

Geoengineering with Charged Droplets

NASA Astrophysics Data System (ADS)

Gokturk, H.

2011-12-01

Water molecules in a droplet are held together by intermolecular forces generated by hydrogen bonding which has a bonding energy of only about 0.2 eV. One can create a more rugged droplet by using an ion as a condensation nucleus. In that case, water molecules are held together by the interaction between the ion and the dipole moments of the water molecules surrounding the ion, in addition to any hydrogen bonding. In this research, properties of such charged droplets were investigated using first principle quantum mechanical calculations. A molecule which exhibits positive electron affinity is a good candidate to serve as the ionic condensation nucleus, because addition of an electron to such a molecule creates an energetically more stable state than the neutral molecule. A good example is the oxygen molecule (O2) where energy of O2 negative (O2-) ion is lower than that of the neutral O2 by about 0.5 eV. Examples of other molecules which have positive electron affinity include ozone (O3), nitrogen dioxide (NO2) and sulfur oxides (SOx, x=1-3). Atomic models used in the calculations consisted of a negative ion of one of the molecules mentioned above surrounded by water molecules. Calculations were performed using the DFT method with B3LYP hybrid functional and Pople type basis sets with polarization and diffuse functions. Energy of interaction between O2- ion and the water molecule was found to be ~0.7 eV. This energy is an order of magnitude greater than the thermal energy of even the highest temperatures encountered in the atmosphere. Once created, charged rugged droplets can survive in hot and dry climates where they can be utilized to create humidity and precipitation. The ion which serves as the nucleus of the droplet can attract not only water molecules but also other dipolar gases in the atmosphere. Such dipolar gases include industrial pollutants, for example nitrogen dioxide (NO2) or sulfur dioxide (SO2). Energy of interaction between O2- ion and pollutant molecules was calculated to be ~0.5 eV for NO2 and ~0.9 eV for SO2. These values are comparable to that of water, hence charged droplets have the potential to serve as scavengers of pollutants in the atmosphere. The charged droplet can also interact with quadrupolar gases depending on the charge distribution of the gas. A quadrupole of interest is carbon dioxide (CO2) where oxygens are slightly negative and carbon is slightly positive in a neutral molecule. When CO2 is in the vicinity of a negative ion, the carbon atom gets attracted to the ion, whereas oxygens are repelled from it. This interaction distorts the linear geometry of CO2, turning it into a small dipole. Energy of interaction between O2- ion and CO2 was calculated to be ~0.3 eV which is smaller than those of the above mentioned dipoles, but still significantly greater than the typical thermal energy at 25 C (~0.03 eV). One can expect the diffusion of atmospheric CO2 into the droplets to be enhanced due to the charge. Hence such droplets can help capture the CO2 in the atmosphere and sequester it simply as rain. Charged droplets can be created using electrical,optical, thermal or other means. A method which utilizes solar energy will be described in the presentation.

North American prairie wetlands are important nonforested land-based carbon storage sites

USGS Publications Warehouse

Euliss, N.H.; Gleason, R.A.; Olness, A.; McDougal, R.L.; Murkin, H.R.; Robarts, R.D.; Bourbonniere, R.A.; Warner, B.G.

2006-01-01

We evaluated the potential of prairie wetlands in North America as carbon sinks. Agricultural conversion has resulted in the average loss of 10.1 Mg ha- 1 of soil organic carbon on over 16 million ha of wetlands in this region. Wetland restoration has potential to sequester 378 Tg of organic carbon over a 10-year period. Wetlands can sequester over twice the organic carbon as no-till cropland on only about 17% of the total land area in the region. We estimate that wetland restoration has potential to offset 2.4% of the annual fossil CO2 emission reported for North America in 1990. ?? 2005 Elsevier B.V. All rights reserved.

Multiphase, multicomponent simulations and experiments of reactive flow, relevant for combining geologic CO2 sequestration with geothermal energy capture

NASA Astrophysics Data System (ADS)

Saar, Martin O.

2011-11-01

Understanding the fluid dynamics of supercritical carbon dioxide (CO2) in brine- filled porous media is important for predictions of CO2 flow and brine displacement during geologic CO2 sequestration and during geothermal energy capture using sequestered CO2 as the subsurface heat extraction fluid. We investigate multiphase fluid flow in porous media employing particle image velocimetry experiments and lattice-Boltzmann fluid flow simulations at the pore scale. In particular, we are interested in the motion of a drop (representing a CO2 bubble) through an orifice in a plate, representing a simplified porous medium. In addition, we study single-phase/multicomponent reactive transport experimentally by injecting water with dissolved CO2 into rocks/sediments typically considered for CO2 sequestration to investigate how resultant fluid-mineral reactions modify permeability fields. Finally, we investigate numerically subsurface CO2 and heat transport at the geologic formation scale.

Geologic CO2 Sequestration: Predicting and Confirming Performance in Oil Reservoirs and Saline Aquifers

NASA Astrophysics Data System (ADS)

Johnson, J. W.; Nitao, J. J.; Newmark, R. L.; Kirkendall, B. A.; Nimz, G. J.; Knauss, K. G.; Ziagos, J. P.

2002-05-01

Reducing anthropogenic CO2 emissions ranks high among the grand scientific challenges of this century. In the near-term, significant reductions can only be achieved through innovative sequestration strategies that prevent atmospheric release of large-scale CO2 waste streams. Among such strategies, injection into confined geologic formations represents arguably the most promising alternative; and among potential geologic storage sites, oil reservoirs and saline aquifers represent the most attractive targets. Oil reservoirs offer a unique "win-win" approach because CO2 flooding is an effective technique of enhanced oil recovery (EOR), while saline aquifers offer immense storage capacity and widespread distribution. Although CO2-flood EOR has been widely used in the Permian Basin and elsewhere since the 1980s, the oil industry has just recently become concerned with the significant fraction of injected CO2 that eludes recycling and is therefore sequestered. This "lost" CO2 now has potential economic value in the growing emissions credit market; hence, the industry's emerging interest in recasting CO2 floods as co-optimized EOR/sequestration projects. The world's first saline aquifer storage project was also catalyzed in part by economics: Norway's newly imposed atmospheric emissions tax, which spurred development of Statoil's unique North Sea Sleipner facility in 1996. Successful implementation of geologic sequestration projects hinges on development of advanced predictive models and a diverse set of remote sensing, in situ sampling, and experimental techniques. The models are needed to design and forecast long-term sequestration performance; the monitoring techniques are required to confirm and refine model predictions and to ensure compliance with environmental regulations. We have developed a unique reactive transport modeling capability for predicting sequestration performance in saline aquifers, and used it to simulate CO2 injection at Sleipner; we are now extending this capability to address CO2-flood EOR/sequestration in oil reservoirs. We have also developed a suite of innovative geophysical and geochemical techniques for monitoring sequestration performance in both settings. These include electromagnetic induction imaging and electrical resistance tomography for tracking migration of immiscible CO2, noble gas isotopes for assessing trace CO2 leakage through the cap rock, and integrated geochemical sampling, analytical, and experimental methods for determining sequestration partitioning among solubility and mineral trapping mechanisms. We have proposed to demonstrate feasibility of the co-optimized EOR/sequestration concept and utility of our modeling and monitoring technologies to design and evaluate its implementation by conducting a demonstration project in the Livermore Oil Field. This small, mature, shallow field, located less than a mile east of Lawrence Livermore National Laboratory, is representative of many potential EOR/sequestration sites in California. In approach, this proposed demonstration is analogous to the Weyburn EOR/CO2 monitoring project, to which it will provide an important complement by virtue of its contrasting depth (immiscible versus Weyburn's miscible CO2 flood) and geologic setting (clay-capped sand versus Weyburn's anhydrite-capped carbonate reservoir).

Spatial variability of upper ocean POC export in the Bay of Bengal and the Indian Ocean determined using particle-reactive 234Th

NASA Astrophysics Data System (ADS)

Subha Anand, S.; Rengarajan, R.; Sarma, V. V. S. S.; Sudheer, A. K.; Bhushan, R.; Singh, S. K.

2017-05-01

The northern Indian Ocean is globally significant for its seasonally reversing winds, upwelled nutrients, high biological production, and expanding oxygen minimum zones. The region acts as sink and source for atmospheric CO2. However, the efficiency of the biological carbon pump to sequester atmospheric CO2 and export particulate organic carbon from the surface is not well known. To quantify the upper ocean carbon export flux and to estimate the efficiency of biological carbon pump in the Bay of Bengal and the Indian Ocean, seawater profiles of total 234Th were measured from surface to 300 m depth at 13 stations from 19.9°N to 25.3°S in a transect along 87°E, during spring intermonsoon period (March-April 2014). Results showed enhanced in situ primary production in the equatorial Indian Ocean and the central Bay of Bengal and varied from 13.2 to 173.8 mmol C m-2 d-1. POC export flux in this region varied from 0 to 7.7 mmol C m-2 d-1. Though high carbon export flux was found in the equatorial region, remineralization of organic carbon in the surface and subsurface waters considerably reduced organic carbon export in the Bay of Bengal. Annually recurring anticyclonic eddies enhanced organic carbon utilization and heterotrophy. Oxygen minimum zone developed due to stratification and poor ventilation was intensified by subsurface remineralization. 234Th-based carbon export fluxes were not comparable with empirical statistical model estimates based on primary production and temperature. Region-specific refinement of model parameters is required to accurately predict POC export fluxes.

Changes in Nitrogen Cycling during Tropical Forest Secondary Succession on Abandoned Pastures

NASA Astrophysics Data System (ADS)

Mirza, S.; Rivera, R. J.; Marin-Spiotta, E.

2017-12-01

Nitrogen (N) plays two important roles in Earth's climate. As a plant nutrient, the availability of N affects plant growth and the uptake of carbon (C) from the atmosphere into plant biomass. The accumulation of C in long-lived biomass and in soils contributes to reducing the amount of CO2 in the atmosphere. Secondly, excess N can lead to the production of N2O, which is a more potent greenhouse than CO2. Humans have altered the cycling of N in terrestrial ecosystems, affecting their potential to sequester C and help mitigate climate change. Land-use change, specifically deforestation and reforestation, can affect N availability for plant growth and N2O production. Long-term agricultural use can deplete nitrogen sources, even in tropical soils where N is not expected to limit productivity. Secondary succession and reforestation can allow for the recovery of N stocks and fluxes, with implications for C cycling and N2O emissions. N limitation in pastures and early successional forests increases the demand for N-fixing tree species, but previous research has shown that there is a greater abundance of N-fixing species in older forests (Batterman et. al 2013). Successional trends in N mineralization and denitrification vary across studies, with some showing greater rates in agricultural soils or in mature forest soils, compared to early successional sites. Here we examine changes in N-fixing species, above and belowground N pools, and N cycling rates in secondary forests on former pastures on Oxisols in the wet tropical forest life zone of Puerto Rico. The availability of a long-term well-replicated chronosequence provides us with the opportunity to study decadal trends in N processes during forest recovery after agricultural abandonment.

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

Doug Cathro

The Lake Charles CCS Project is a large-scale industrial carbon capture and sequestration (CCS) project which will demonstrate advanced technologies that capture and sequester carbon dioxide (CO{sub 2}) emissions from industrial sources into underground formations. Specifically the Lake Charles CCS Project will accelerate commercialization of large-scale CO{sub 2} storage from industrial sources by leveraging synergy between a proposed petroleum coke to chemicals plant (the LCC Gasification Project) and the largest integrated anthropogenic CO{sub 2} capture, transport, and monitored sequestration program in the U.S. Gulf Coast Region. The Lake Charles CCS Project will promote the expansion of EOR in Texas andmore » Louisiana and supply greater energy security by expanding domestic energy supplies. The capture, compression, pipeline, injection, and monitoring infrastructure will continue to sequester CO{sub 2} for many years after the completion of the term of the DOE agreement. The objectives of this project are expected to be fulfilled by working through two distinct phases. The overall objective of Phase 1 was to develop a fully definitive project basis for a competitive Renewal Application process to proceed into Phase 2 - Design, Construction and Operations. Phase 1 includes the studies attached hereto that will establish: the engineering design basis for the capture, compression and transportation of CO{sub 2} from the LCC Gasification Project, and the criteria and specifications for a monitoring, verification and accounting (MVA) plan at the Hastings oil field in Texas. The overall objective of Phase 2, provided a successful competitive down-selection, is to execute design, construction and operations of three capital projects: (1) the CO{sub 2} capture and compression equipment, (2) a Connector Pipeline from the LLC Gasification Project to the Green Pipeline owned by Denbury and an affiliate of Denbury, and (3) a comprehensive MVA system at the Hastings oil field.« less

DE-SC0004118 (Wong & Lindquist). Final Report: Changes of Porosity, Permeability and Mechanical Strength Induced by Carbon Dioxide Sequestration.

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

WONG, TENG-FONG; Lindquist, Brent

In the context of CO{sub 2} sequestration, the overall objective of this project is to conduct a systematic investigation of how the flow of the acidic, CO{sub 2} saturated, single phase component of the injected/sequestered fluid changes the microstructure, permeability and strength of sedimentary rocks, specifically limestone and sandstone samples. Hydromechanical experiments, microstructural observations and theoretical modeling on multiple scales were conducted.

Breeding crop plants with deep roots: their role in sustainable carbon, nutrient and water sequestration

PubMed Central

Kell, Douglas B.

2011-01-01

Background The soil represents a reservoir that contains at least twice as much carbon as does the atmosphere, yet (apart from ‘root crops’) mainly just the above-ground plant biomass is harvested in agriculture, and plant photosynthesis represents the effective origin of the overwhelming bulk of soil carbon. However, present estimates of the carbon sequestration potential of soils are based more on what is happening now than what might be changed by active agricultural intervention, and tend to concentrate only on the first metre of soil depth. Scope Breeding crop plants with deeper and bushy root ecosystems could simultaneously improve both the soil structure and its steady-state carbon, water and nutrient retention, as well as sustainable plant yields. The carbon that can be sequestered in the steady state by increasing the rooting depths of crop plants and grasses from, say, 1 m to 2 m depends significantly on its lifetime(s) in different molecular forms in the soil, but calculations (http://dbkgroup.org/carbonsequestration/rootsystem.html) suggest that this breeding strategy could have a hugely beneficial effect in stabilizing atmospheric CO2. This sets an important research agenda, and the breeding of plants with improved and deep rooting habits and architectures is a goal well worth pursuing. PMID:21813565

Breeding crop plants with deep roots: their role in sustainable carbon, nutrient and water sequestration.

PubMed

Kell, Douglas B

2011-09-01

The soil represents a reservoir that contains at least twice as much carbon as does the atmosphere, yet (apart from 'root crops') mainly just the above-ground plant biomass is harvested in agriculture, and plant photosynthesis represents the effective origin of the overwhelming bulk of soil carbon. However, present estimates of the carbon sequestration potential of soils are based more on what is happening now than what might be changed by active agricultural intervention, and tend to concentrate only on the first metre of soil depth. Breeding crop plants with deeper and bushy root ecosystems could simultaneously improve both the soil structure and its steady-state carbon, water and nutrient retention, as well as sustainable plant yields. The carbon that can be sequestered in the steady state by increasing the rooting depths of crop plants and grasses from, say, 1 m to 2 m depends significantly on its lifetime(s) in different molecular forms in the soil, but calculations (http://dbkgroup.org/carbonsequestration/rootsystem.html) suggest that this breeding strategy could have a hugely beneficial effect in stabilizing atmospheric CO(2). This sets an important research agenda, and the breeding of plants with improved and deep rooting habits and architectures is a goal well worth pursuing.

Production, process optimization and molecular characterization of polyhydroxyalkanoate (PHA) by CO2 sequestering B. cereus SS105.

PubMed

Maheshwari, Neha; Kumar, Madan; Thakur, Indu Shekhar; Srivastava, Shaili

2018-04-01

Carbon dioxide sequestering bacterial strains were previously isolated from free air CO 2 enriched (FACE) soil. In the present study, these strains were screened for PHA accumulation and Bacillus cereus SS105 was found to be the most prominent PHA accumulating strain on sodium bicarbonate and molasses as carbon source. This strain was further characterized by Spectrofluorometric method and Confocal microscopy after staining with Nile red. PHA granules in inclusion bodies were visualized by Transmission Electron Microscopy. The PHA and its monomer composition were characterized by GC-MS followed by FTIR and NMR. The genetic basis of PHA production was confirmed by the amplification, cloning and analysis of PHA biosynthesis genes phaR, phaB and phaC from B. cereus with the degenerate primers. The PHA production was further optimized by Response Surface Methodology and the percent increase observed after optimization was 55.16% (w/v). Copyright © 2018 Elsevier Ltd. All rights reserved.

Greenhouse Gas Fluxes at the Tablelands, NL, Canada: A Site of Active Serpentinization

NASA Astrophysics Data System (ADS)

Morrill, P. L.; Morrissey, L. S.; Cumming, E.

2016-12-01

Active sites of serpentinization have been proposed as sites for carbon capture and storage (CCS) projects. However, in addition to their ability to convert carbon dioxide to carbonate rock, sites of serpentinization also have the potential release methane, which is a more power greenhouse gas than carbon dioxide. Very little is known about the natural flux of carbon dioxide sequestered and methane released into the atmosphere from active sites of serpentinization. In this study we measured carbon dioxide, methane, and nitrous oxide gas fluxes at a pool of ultra-basic water discharging from serpentinized rock in Winterhouse Canyon, Gros Morne, Newfoundland. We found that the flux of methane released was 4.6 x 10-7 mol/m2/min and the carbon dioxide sequestered was 1.9 x 10-5 mol/m2/min, while the concentrations of nitrous oxide showed little change. Based on these fluxes we calculated predictive climate change parameters such as net radiative forcing and global warming potential which predicted that despite the methane being released the site still had an overall long-term atmospheric cooling effect based on the natural rate of carbon dioxide sequestration.

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

Cannon, Gordon C.; Heinhorst, Sabine; Kerfeld, Cheryl A.

Cyanobacteria and some chemoautotrophic bacteria are able to grow in environments with limiting CO2 concentrations by employing a CO2-concentrating mechanism (CCM) that allows them to accumulate inorganic carbon in their cytoplasm to concentrations several orders of magnitude higher than that on the outside. The final step of this process takes place in polyhedral protein microcompartments known as carboxysomes, which contain the majority of the CO2-fixing enzyme, RubisCO. The efficiency of CO2 fixation by the sequestered RubisCO is enhanced by co-localization with a specialized carbonic anhydrase that catalyzes dehydration of the cytoplasmic bicarbonate and ensures saturation of RubisCO with its substrate,more » CO2. There are two genetically distinct carboxysome types that differ in their protein composition and in the carbonic anhydrase(s) they employ. Here we review the existing information concerning the genomics, structure and enzymology of these uniquely adapted carbonic anhydrases, which are of fundamental importance in the global carbon cycle.« less

Two-way feedback between biology and deep Earth processes

NASA Astrophysics Data System (ADS)

Sleep, N. H.; Pope, E.; Bird, D.

2012-12-01

The presence of the metamorphic products of banded iron formation and black shale indicate that the Earth teemed with life by the time of the earliest preserved rocks, ca. 3.85 Ga. Iron and sulfur-based anoxygenic photosynthesis with full carbon cycles was present by this time. The pH of the ocean was ~8. The lack of older rock record cloaks pre-biotic evolution and the origin of life. Nascent and early life obtained energy from chemical disequilibria in rocks rather than sunlight. Appraising putative rock pre-biological environments is difficult in that life has modified the composition of the atmosphere, the hydrosphere, and sedimentary rocks. It has greatly affected the composition of crystalline crustal rocks and measurably modified the mantle. Conversely, hard crustal rocks and the mantle likely sequester a very ancient record of last resort. Theory provides additional insight. The Earth's surface and interior cooled following the moon-forming impact. The oceans passed through conditions favored by thermophile organisms before becoming clement. Ocean pH was ~6 and bars of CO2 existed in the atmosphere. Subduction removed the CO2 into the mantle before the time of rock record. Serpentinite likely existed in land, tidal, and marine environments as it does today. Seafloor spreading and arc volcanism likely drove hydrothermal circulation. The late heavy bombardment occurred after ca. 4.1 Ga; low heat flow environments and hence habitable subsurface refugia existed. It is conceivable that one or a few ocean-boiling impacts left thermophile survivors in their wake. Overall, the molecular biology of extant life likely conserves features that relate to its earliest abodes.

The spatial extent of agriculturally-induced topsoil removal in the Midwestern United States

NASA Astrophysics Data System (ADS)

Thaler, E.; Larsen, I. J.; Yu, Q.; Keiluweit, M.

2017-12-01

Human-induced erosion of soil organic carbon (SOC) degrades soils, leading to decreased crop yields. Here we develop a novel approach for mapping the spatial distribution of complete topsoil loss in agricultural landscapes, focusing on the Midwestern U.S. We used the ferric iron index (FeI) derived from high-resolution satellite imagery to map Fe-rich subsoil exposed by the loss of carbon-rich topsoil. Integrating topographic curvature derived from high resolution topographic data with FeI values demonstrates that FeI values are lowest in concave hollows where eroded soil accumulates, and increase linearly with topographic curvature on convex hilltops. The relationship between FeI and curvature indicates diffusion-like erosion by tillage is a dominant mechanism of soil loss, a mechanism generally not included in soil loss prediction in the U.S. Moreover, the FeI and curvature data indicate SOC-rich topsoil has been completely removed from hilltops, exposing Fe-rich subsoil. This interpretation supported by measurements of FeI using laboratory spectra, extractable-Fe, and organic C from two soil profiles from native prairies, which preserve the pre-agricultural soil profile. FeI increased sharply from the topsoil through the subsoil and total C and extractable Fe content are negatively correlated in both profiles. We calculated topographic curvature for 3.8 x105 km2 of the formerly-glaciated Midwestern U.S. using LiDAR data and found that convex topography, where FeI values suggest topsoil has been completely stripped, covers half of the landscape. Assuming complete removal of original SOC on all hilltops, we estimate that 784 Tg of C has been removed since cultivation began in the mid-1800s and that the SOC decline results in billions of dollars in annual economic losses from decreased crop yields. Restoration of eroded SOC has been proposed as a method to sequester atmospheric CO2 while simultaneously increasing crop yields, and our estimates suggest that replenishing eroded SOC within the Midwestern U.S. to pre-settlement levels could sequester 2900 Tg of CO2, equivalent to more than half of 2016 U.S. CO2 emissions. Our study highlights both the necessity to incorporate tillage into soil erosion models and the potential for SOC restoration to increase crop yields and offset carbon emissions.

Effects of media and species on soil CO2 efflux in the landscape

USDA-ARS?s Scientific Manuscript database

Increasing concentrations of greenhouse gases (GHG) including carbon dioxide, methane, and nitrous oxide are widely believed to be the main contributing factors leading to global climate change. The horticulture industry has the potential to improve GHG conditions through sequestering carbon (C) in ...

The costing of carbon credits from ocean nourishment plants.

PubMed

Shoji, K; Jones, I S

2001-09-28

Ocean nourishment is a process for stimulating the sequestration of atmospheric carbon dioxide in the deep ocean by providing the nutrients needed to enhance the production of phytoplankton. The carbon dioxide sink thus created, can be used to generate tradeable carbon credits. The costs of sequestering carbon by the process of ocean nourishment have been estimated using as a basis, the previous experience in nitrogen fixing of Toyo Engineering Corporation. While there are uncertainties about the biological uptake efficiency, these introduce only a moderate uncertainty in our overall estimates of costs. The major determinants of the costs are the interest that must be paid on capital and the cost of the feedstock, natural gas. We have used for discussion purposes, an interest rate of 4-8% per annum and natural gas costs of US$0.5-$2 per GJ. The costs of carbon credits lie in the range US$6.70-$12.40 per tonne of carbon dioxide emissions sequestered. It should be noted that we have adopted the measure of carbon avoided by non-emission, because of the complex partitioning of anthropogenic carbon between the atmosphere, land and ocean.

Terrestrial nitrogen–carbon cycle interactions at the global scale

PubMed Central

Zaehle, S.

2013-01-01

Interactions between the terrestrial nitrogen (N) and carbon (C) cycles shape the response of ecosystems to global change. However, the global distribution of nitrogen availability and its importance in global biogeochemistry and biogeochemical interactions with the climate system remain uncertain. Based on projections of a terrestrial biosphere model scaling ecological understanding of nitrogen–carbon cycle interactions to global scales, anthropogenic nitrogen additions since 1860 are estimated to have enriched the terrestrial biosphere by 1.3 Pg N, supporting the sequestration of 11.2 Pg C. Over the same time period, CO2 fertilization has increased terrestrial carbon storage by 134.0 Pg C, increasing the terrestrial nitrogen stock by 1.2 Pg N. In 2001–2010, terrestrial ecosystems sequestered an estimated total of 27 Tg N yr−1 (1.9 Pg C yr−1), of which 10 Tg N yr−1 (0.2 Pg C yr−1) are due to anthropogenic nitrogen deposition. Nitrogen availability already limits terrestrial carbon sequestration in the boreal and temperate zone, and will constrain future carbon sequestration in response to CO2 fertilization (regionally by up to 70% compared with an estimate without considering nitrogen–carbon interactions). This reduced terrestrial carbon uptake will probably dominate the role of the terrestrial nitrogen cycle in the climate system, as it accelerates the accumulation of anthropogenic CO2 in the atmosphere. However, increases of N2O emissions owing to anthropogenic nitrogen and climate change (at a rate of approx. 0.5 Tg N yr−1 per 1°C degree climate warming) will add an important long-term climate forcing. PMID:23713123

Terrestrial nitrogen-carbon cycle interactions at the global scale.

PubMed

Zaehle, S

2013-07-05

Interactions between the terrestrial nitrogen (N) and carbon (C) cycles shape the response of ecosystems to global change. However, the global distribution of nitrogen availability and its importance in global biogeochemistry and biogeochemical interactions with the climate system remain uncertain. Based on projections of a terrestrial biosphere model scaling ecological understanding of nitrogen-carbon cycle interactions to global scales, anthropogenic nitrogen additions since 1860 are estimated to have enriched the terrestrial biosphere by 1.3 Pg N, supporting the sequestration of 11.2 Pg C. Over the same time period, CO2 fertilization has increased terrestrial carbon storage by 134.0 Pg C, increasing the terrestrial nitrogen stock by 1.2 Pg N. In 2001-2010, terrestrial ecosystems sequestered an estimated total of 27 Tg N yr(-1) (1.9 Pg C yr(-1)), of which 10 Tg N yr(-1) (0.2 Pg C yr(-1)) are due to anthropogenic nitrogen deposition. Nitrogen availability already limits terrestrial carbon sequestration in the boreal and temperate zone, and will constrain future carbon sequestration in response to CO2 fertilization (regionally by up to 70% compared with an estimate without considering nitrogen-carbon interactions). This reduced terrestrial carbon uptake will probably dominate the role of the terrestrial nitrogen cycle in the climate system, as it accelerates the accumulation of anthropogenic CO2 in the atmosphere. However, increases of N2O emissions owing to anthropogenic nitrogen and climate change (at a rate of approx. 0.5 Tg N yr(-1) per 1°C degree climate warming) will add an important long-term climate forcing.

Landscape-level controls on dissolved carbon flux from diverse catchments of the circumboreal

USGS Publications Warehouse

Tank, Suzanne; Frey, Karen E.; Striegl, Robert G.; Raymond, Peter A.; Holmes, R. Max; McClelland, James W.; Peterson, Bruce J.

2012-01-01

While much of the dissolved organic carbon (DOC) within rivers is destined for mineralization to CO2, a substantial fraction of riverine bicarbonate (HCO3-) flux represents a CO2 sink, as a result of weathering processes that sequester CO2 as HCO3-. We explored landscape-level controls on DOC and HCO3- flux in subcatchments of the boreal, with a specific focus on the effect of permafrost on riverine dissolved C flux. To do this, we undertook a multivariate analysis that partitioned the variance attributable to known, key regulators of dissolved C flux (runoff, lithology, and vegetation) prior to examining the effect of permafrost, using riverine biogeochemistry data from a suite of subcatchments drawn from the Mackenzie, Yukon, East, and West Siberian regions of the circumboreal. Across the diverse catchments that we study, controls on HCO3- flux were near-universal: runoff and an increased carbonate rock contribution to weathering (assessed as riverwater Ca:Na) increased HCO3- yields, while increasing permafrost extent was associated with decreases in HCO3-. In contrast, permafrost had contrasting and region-specific effects on DOC yield, even after the variation caused by other key drivers of its flux had been accounted for. We used ionic ratios and SO4 yields to calculate the potential range of CO2 sequestered via weathering across these boreal subcatchments, and show that decreasing permafrost extent is associated with increases in weathering-mediated CO2 fixation across broad spatial scales, an effect that could counterbalance some of the organic C mineralization that is predicted with declining permafrost.

Effects of nutrient ratios and carbon dioxide bio-sequestration on biomass growth of Chlorella sp. in bubble column photobioreactor.

PubMed

Vo, Hoang-Nhat-Phong; Bui, Xuan-Thanh; Nguyen, Thanh-Tin; Nguyen, Dinh Duc; Dao, Thanh-Son; Cao, Ngoc-Dan-Thanh; Vo, Thi-Kim-Quyen

2018-08-01

Photobioreactor technology, especially bubble column configuration, employing microalgae cultivation (e.g., Chlorella sp.), is an ideal man-made environment to achieve sufficient microalgae biomass through its strictly operational control. Nutrients, typically N and P, are necessary elements in the cultivation process, which determine biomass yield and productivity. Specifically, N:P ratios have certain effects on microalgae's biomass growth. It is also attractive that microalgae can sequester CO 2 by using that carbon source for photosynthesis and, subsequently, reducing CO 2 emission. Therefore, this study aims to investigate the effect of N:P ratios on Chlorella sp.'s growth, and to study the dynamic of CO 2 fixation in the bubble column photobioreactor. According to our results, N:P ratio of 15:1 could produce the highest biomass yield (3568 ± 158 mg L -1 ). The maximum algae concentration was 105 × 10 6  cells mL -1 , receiving after 92 h. Chlorella sp. was also able to sequester CO 2 at 28 ± 1.2%, while the specific growth rate and carbon fixation rate were observed at 0.064 h -1 and 68.9 ± 1.91 mg L -1  h -1 , respectively. The types of carbon sources (e.g., organic and inorganic carbon) possessed potential impact on microalgae's cultivation. Copyright © 2018 Elsevier Ltd. All rights reserved.

Forest and grassland cover types reduce net greenhouse gas emissions from agricultural soils.

PubMed

Baah-Acheamfour, Mark; Carlyle, Cameron N; Lim, Sang-Sun; Bork, Edward W; Chang, Scott X

2016-11-15

Western Canada's prairie region is extensively cultivated for agricultural production, which is a large source of greenhouse gas emissions. Agroforestry systems are common land uses across Canada, which integrate trees into the agricultural landscape and could play a substantial role in sequestering carbon and mitigating increases in atmospheric GHG concentrations. We measured soil CO2, CH4 and N2O fluxes and the global warming potential of microbe-mediated net greenhouse gas emissions (GWPm) in forest and herbland (areas without trees) soils of three agroforestry systems (hedgerow, shelterbelt and silvopasture) over two growing seasons (May through September in 2013 and 2014). We measured greenhouse gas fluxes and environmental conditions at 36 agroforestry sites (12 sites for each system) located along a south-north oriented soil/climate gradient of increasing moisture availability in central Alberta, Canada. The temperature sensitivity of soil CO2 emissions was greater in herbland (4.4) than in forest (3.1), but was not different among agroforestry systems. Over the two seasons, forest soils had 3.4% greater CO2 emission, 36% higher CH4 uptake, and 66% lower N2O emission than adjacent herbland soils. Combining the CO2 equivalents of soil CH4 and N2O fluxes with the CO2 emitted via heterotrophic (microbial) respiration, forest soils had a smaller GWPm than herbland soils (68 and 89kgCO2ha(-1), respectively). While emissions of total CO2 were silvopasture>hedgerow>shelterbelt, soils under silvopasture had 5% lower heterotrophic respiration, 15% greater CH4 uptake, and 44% lower N2O emission as compared with the other two agroforestry systems. Overall, the GWPm of greenhouse gas emissions was greater in hedgerow (88) and shelterbelt (85) than in the silvopasture system (76kgCO2ha(-1)). High GWPm in the hedgerow and shelterbelt systems reflects the greater contribution from the monoculture annual crops within these systems. Opportunities exist for reducing soil greenhouse gas emissions and mitigating climate change by promoting the establishment of perennial vegetation in the agricultural landscape. Copyright © 2016 Elsevier B.V. All rights reserved.

In-situ observation for growth of hierarchical metal-organic frameworks and their self-sequestering mechanism for gas storage

NASA Astrophysics Data System (ADS)

Hyo Park, Jung; Min Choi, Kyung; Joon Jeon, Hyung; Jung Choi, Yoon; Ku Kang, Jeung

2015-07-01

Although structures with the single functional constructions and micropores were demonstrated to capture many different molecules such as carbon dioxide, methane, and hydrogen with high capacities at low temperatures, their feeble interactions still limit practical applications at room temperature. Herein, we report in-situ growth observation of hierarchical pores in pomegranate metal-organic frameworks (pmg-MOFs) and their self-sequestering storage mechanism, not observed for pristine MOFs. Direct observation of hierarchical pores inside the pmg-MOF was evident by in-situ growth X-ray measurements while self-sequestering storage mechanism was revealed by in-situ gas sorption X-ray analysis and molecular dynamics simulations. The results show that meso/macropores are created at the early stage of crystal growth and then enclosed by micropore crystalline shells, where hierarchical pores are networking under self-sequestering mechanism to give enhanced gas storage. This pmg-MOF gives higher CO2 (39%) and CH4 (14%) storage capacity than pristine MOF at room temperature, in addition to fast kinetics with robust capacity retention during gas sorption cycles, thus giving the clue to control dynamic behaviors of gas adsorption.

Carbon Abatement and Emissions Associated with the Gasification of Walnut Shells for Bioenergy and Biochar Production.

PubMed

Pujol Pereira, Engil Isadora; Suddick, Emma C; Six, Johan

2016-01-01

By converting biomass residue to biochar, we could generate power cleanly and sequester carbon resulting in overall greenhouse gas emissions (GHG) savings when compared to typical fossil fuel usage and waste disposal. We estimated the carbon dioxide (CO2) abatements and emissions associated to the concurrent production of bioenergy and biochar through biomass gasification in an organic walnut farm and processing facility in California, USA. We accounted for (i) avoided-CO2 emissions from displaced grid electricity by bioenergy; (ii) CO2 emissions from farm machinery used for soil amendment of biochar; (iii) CO2 sequestered in the soil through stable biochar-C; and (iv) direct CO2 and nitrous oxide (N2O) emissions from soil. The objective of these assessments was to pinpoint where the largest C offsets can be expected in the bioenergy-biochar chain. We found that energy production from gasification resulted in 91.8% of total C offsets, followed by stable biochar-C (8.2% of total C sinks), offsetting a total of 107.7 kg CO2-C eq Mg-1 feedstock. At the field scale, we monitored gas fluxes from soils for 29 months (180 individual observations) following field management and precipitation events in addition to weekly measurements within three growing seasons and two tree dormancy periods. We compared four treatments: control, biochar, compost, and biochar combined with compost. Biochar alone or in combination with compost did not alter total N2O and CO2 emissions from soils, indicating that under the conditions of this study, biochar-prompted C offsets may not be expected from the mitigation of direct soil GHG emissions. However, this study revealed a case where a large environmental benefit was given by the waste-to-bioenergy treatment, addressing farm level challenges such as waste management, renewable energy generation, and C sequestration.

Carbon Abatement and Emissions Associated with the Gasification of Walnut Shells for Bioenergy and Biochar Production

PubMed Central

Pujol Pereira, Engil Isadora; Suddick, Emma C.; Six, Johan

2016-01-01

By converting biomass residue to biochar, we could generate power cleanly and sequester carbon resulting in overall greenhouse gas emissions (GHG) savings when compared to typical fossil fuel usage and waste disposal. We estimated the carbon dioxide (CO2) abatements and emissions associated to the concurrent production of bioenergy and biochar through biomass gasification in an organic walnut farm and processing facility in California, USA. We accounted for (i) avoided-CO2 emissions from displaced grid electricity by bioenergy; (ii) CO2 emissions from farm machinery used for soil amendment of biochar; (iii) CO2 sequestered in the soil through stable biochar-C; and (iv) direct CO2 and nitrous oxide (N2O) emissions from soil. The objective of these assessments was to pinpoint where the largest C offsets can be expected in the bioenergy-biochar chain. We found that energy production from gasification resulted in 91.8% of total C offsets, followed by stable biochar-C (8.2% of total C sinks), offsetting a total of 107.7 kg CO2-C eq Mg-1 feedstock. At the field scale, we monitored gas fluxes from soils for 29 months (180 individual observations) following field management and precipitation events in addition to weekly measurements within three growing seasons and two tree dormancy periods. We compared four treatments: control, biochar, compost, and biochar combined with compost. Biochar alone or in combination with compost did not alter total N2O and CO2 emissions from soils, indicating that under the conditions of this study, biochar-prompted C offsets may not be expected from the mitigation of direct soil GHG emissions. However, this study revealed a case where a large environmental benefit was given by the waste-to-bioenergy treatment, addressing farm level challenges such as waste management, renewable energy generation, and C sequestration. PMID:26963623

Downhole fluid injection systems, CO₂ sequestration methods, and hydrocarbon material recovery methods

DOEpatents

Schaef, Herbert T.; McGrail, B. Peter

2015-07-28

Downhole fluid injection systems are provided that can include a first well extending into a geological formation, and a fluid injector assembly located within the well. The fluid injector assembly can be configured to inject a liquid CO₂/H₂O-emulsion into the surrounding geological formation. CO₂ sequestration methods are provided that can include exposing a geological formation to a liquid CO₂/H₂O-emulsion to sequester at least a portion of the CO₂ from the emulsion within the formation. Hydrocarbon material recovery methods are provided that can include exposing a liquid CO₂/H₂O-emulsion to a geological formation having the hydrocarbon material therein. The methods can include recovering at least a portion of the hydrocarbon material from the formation.

HARNESSING THE CHEMISTRY OF CO2

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

Louie, Janis

2010-05-11

Our research program is broadly focused on activating CO{sub 2} through the use of organic and organometallic based catalysts. Some of our methods have centered on annulation reactions of unsaturated hydrocarbons (and carbonyl substrates) to provide a diverse array of carbocycles and heterocycles. We use a combination of catalyst discovery and optimization in conjunction with classical physical organic chemistry to elucidate the key mechanistic features of the cycloaddition reactions such that the next big advances in catalyst development can be made. Key to all of our cycloaddition reactions is the use of a sterically hindered, electron donating N heterocyclic carbenemore » (NHC) ligand, namely IPr (or SIPr), in conjunction with a low valent nickel pre-catalyst. The efficacy of this ligand is two-fold: (1) the high {delta}-donating ability of the NHC increases the nucleophilicity of the metal center which thereby facilitates interaction with the electrophilic carbonyl and (2) the steric hindrance prevents an otherwise competitive side reaction involving only the alkyne substrate. Such a system has allowed for the facile cycloaddition to prepare highly functionalized pyrones, pyridones, pyrans, as well as novel carbocycles. Importantly, all reactions proceed under extremely mild conditions (room temperature, atmospheric pressures, and short reaction times), require only catalytic amounts of Ni/NHC and readily available starting materials, and afford annulated products in excellent yields. Our current focus revolves around understanding the fundamental processes that govern these cycloadditions such that the next big advance in the cyclization chemistry of CO{sub 2} can be made. Concurrent to our annulation chemistry is our investigation of the potential for imidazolylidenes to function as thermally-actuated CO{sub 2} sequestering and delivery agents.« less

Dissolution of steel slags in aqueous media.

PubMed

Yadav, Shashikant; Mehra, Anurag

2017-07-01

Steel slag is a major industrial waste in steel industries, and its dissolution behavior in water needs to be characterized in the larger context of its potential use as an agent for sequestering CO 2 . For this purpose, a small closed system batch reactor was used to conduct the dissolution of steel slags in an aqueous medium under various dissolution conditions. In this study, two different types of steel slags were procured from steel plants in India, having diverse structural features, mineralogical compositions, and particle sizes. The experiment was performed at different temperatures for 240 h of dissolution at atmospheric pressure. The dissolution rates of major and minor slag elements were quantified through liquid-phase elemental analysis using an inductively coupled plasma atomic emission spectroscopy at different time intervals. Advanced analytical techniques such as field emission gun-scanning electron microscope, energy-dispersive X-ray, BET, and XRD were also used to analyze mineralogical and structural changes in the slag particles. High dissolution of slags was observed irrespective of the particle size distribution, which suggests high carbonation potential. Concentrations of toxic heavy metals in the leachate were far below maximum acceptable limits. Thus, the present study investigates the dissolution behavior of different mineral ions of steel slag in aqueous media in light of its potential application in CO 2 sequestration.

Estimation of weathering rates and CO2 drawdown based on solute load: Significance of granulites and gneisses dominated weathering in the Kaveri River basin, Southern India

NASA Astrophysics Data System (ADS)

Pattanaik, J. K.; Balakrishnan, S.; Bhutani, R.; Singh, P.

2013-11-01

The solute load of the Kaveri River (South India) and its tributaries draining diverse Precambrian terrains during pre-monsoon and monsoon periods was determined. Using average annual flow, total drainage area and atmospheric input corrected major ion concentrations of these rivers chemical weathering rates, annual fluxes of different ionic species to the ocean and CO2 consumption rates were estimated. Bicarbonate is the most dominant ion (27-79% of anion budget) in all the river samples collected during monsoon period followed by Ca2+, whereas, in case of pre-monsoon water samples Na+ is the most dominant ion (in meq/l). Two approaches were adopted to estimate silicate and carbonate weathering rates in the drainage basin. At Musuri silicate weathering rate (SWR) is 9.44 ± 0.29 tons/km2/a and carbonate weathering rate (CWR) is 1.46 ± 0.16 tons/km2/a. More than 90% of the total ionic budget is derived from weathering of silicates in the Kaveri basin. CO2 consumption rate in the basin for silicate weathering FCO2sil is 3.83 ± 0.12 × 105 mol/km2/a (upper limit), which is comparable with the Himalayan rivers at upper reaches. For carbonate weathering (FCO2carb) CO2 consumption rate is 0.15 ± 0.03 × 105 mol/km2/a in the Kaveri basin. The lower limit of CO2 consumption rate corrected for H2SO4 during silicate and carbonate weathering is FCO2sil is 3.24 × 1005 mol/km2/a and FCO2carb 0.13 × 105 mol/km2/a respectively. CO2 sequestered due to silicate weathering in the Kaveri basin is 25.41 (±0.82) × 109 mol/a which represents 0.21 (±0.01)% of global CO2 drawdown. This may be due to tropical climatic condition, high rainfall during both SW and NE monsoon and predominance of silicate rocks in the Kaveri basin.

INCORPORATING WETLANDS IN WATER QUALITY TRADING PROGRAMS: ECONOMIC AND ECOLOGICAL CONSIDERATIONS

EPA Science Inventory

Water quality trading has grown in popularity and scope in recent years owing to its potential as a flexible low cost way to achieve water quality goals, especially nutrient removal goals. Wetlands probide a variety of ecosystem services. They can sequester CO2, they can provide ...

SHARAD Finds Voluminous CO2 Ice Sequestered in the Martian South Polar Layered Deposits

NASA Astrophysics Data System (ADS)

Phillips, R. J.; Davis, B. J.; Byrne, S.; Campbell, B. A.; Carter, L. M.; Haberle, R. M.; Holt, J. W.; Kahre, M. A.; Nunes, D. C.; Plaut, J. J.; Putzig, N. E.; Smith, I. B.; Smrekar, S. E.; Tanaka, K. L.; Titus, T. N.

2010-12-01

The SHARAD instrument on the Mars Reconnaissance Orbiter (MRO) mission has carried out systematic radar soundings of the layered deposits at both martian polar regions. While well-organized sets of radar reflectors are ubiquitous in the North Polar Layered Deposits, those in the South Polar Layered Deposits (SPLD) are limited to specific regions, and it is difficult to map SPLD-wide radar stratigraphy. What is evident in the radar observations are four regional reflection-free zones (RFZ) distinguished qualitatively by their radar characteristics. They are up to a kilometer in thickness and extend downward from near the surface. One such zone (RFZ3) occurs beneath the South Polar Residual Cap (SPRC), which is composed of ~5 m of solid CO2 underlain by an apparently thin layer of water ice. Using a correlation technique, we inverted for the real permittivity, ɛ', on each of 41 usable SHARAD orbits over RFZ3. The results were mean values of ɛ' = 2.0 or 2.1, with a σ of 0.2. A secondary technique based on the “smoothest” solution gave similar results. These values are exceptionally close to the laboratory-measured permittivity value of bulk CO2 ice [Pettinelli et al., 2003] and distant from the bulk water ice value (ɛ' = 3.15); water ice is the dominant volatile in the SPLD. An alternative hypothesis for ɛ' = 2.0-2.1 is that the RFZ3 material is porous water ice, but this can be strongly discounted based on theoretical and empirical models of ɛ' of porous water ice vs. thickness. By the same arguments, the proposed CO2 material also cannot be very porous, and ɛ' should be close to the bulk value. With the permittivity estimates, radar time delays were converted to depth, and for RFZ3 a mean thickness of 210-220 m and a volume of 4,200-4,400 km3 result. This is unlikely to be the entire volume because MRO’s orbital inclination precludes SHARAD sounding poleward of ~87°S, where RFZ3 appears to extend. We do find a very good spatial correlation of RFZ3 with the stratigraphic unit (named “Aa3”) immediately beneath the SPRC [Kolb et al., 2006] and use this geologic unit as a basis for extrapolation, yielding a volume estimate range of 9,500 to 12,500 km3. For comparison, the CO2 in the SPRC is estimated to be < 380 km3 [Thomas et al., 2009]. The equivalent atmospheric pressure of the extrapolated RFZ3 volume is 4-5 mbar, competing in magnitude with the current atmospheric pressure of 6-7 mbar. We have searched the past million year orbit history of Mars for periods when insolation at the south pole would likely render the proposed CO2 mass unstable and are carrying out GCM simulations to evaluate the climate regime at those times with 10-12 mbar of CO2 in the atmosphere. The other three reflection-free zones may also contain a component of CO2, but the reflector geometry is not favorable for estimating permittivity.

Geological Carbon Sequestration in the Ohio River Valley: An Evaluation of Possible Target Formations

NASA Astrophysics Data System (ADS)

Dalton, T. A.; Daniels, J. J.

2009-12-01

The development of geological carbon sequestration within the Ohio River Valley is of major interest to the national electricity and coal industries because the Valley is home to a heavy concentration of coal-burning electricity generation plants and the infrastructure is impossible to eliminate in the short-term. It has been determined by Ohio's politicians and citizenry that the continued use of coal in this region until alternative energy supplies are available will be necessary over the next few years. Geologic sequestration is the only possible means of keeping the CO2 out of the atmosphere in the region. The cost of the sequestration effort greatly decreases CO2 emissions by sequestering CO2 directly on site of these plants, or by minimizing the distance between fossil-fueled generation and sequestration (i.e., by eliminating the cost of transportation of supercritical CO2 from plant to sequestration site). Thus, the practicality of CO2 geologic sequestration within the Ohio River Valley is central to the development of such a commercial effort. Though extensive work has been done by the Regional Partnerships of the DOE/NETL in the characterization of general areas for carbon sequestration throughout the nation, few projects have narrowed their focus into a single geologic region in order to evaluate the sites of greatest commercial potential. As an undergraduate of the Earth Sciences at Ohio State, I have engaged in thorough research to obtain a detailed understanding of the geology of the Ohio River Valley and its potential for commercial-scale carbon sequestration. Through this research, I have been able to offer an estimate of the areas of greatest interest for CO2 geologic sequestration. This research has involved petrological, mineralogical, geochemical, and geophysical analyses of four major reservoir formations within Ohio—the Rose Run, the Copper Ridge, the Clinton, and the Oriskany—along with an evaluation of the possible effects of injection into these saline reservoirs.

How organic carbon derived from multiple sources contributes to carbon sequestration processes in a shallow coastal system?

PubMed Central

Watanabe, Kenta; Kuwae, Tomohiro

2015-01-01

Carbon captured by marine organisms helps sequester atmospheric CO2, especially in shallow coastal ecosystems, where rates of primary production and burial of organic carbon (OC) from multiple sources are high. However, linkages between the dynamics of OC derived from multiple sources and carbon sequestration are poorly understood. We investigated the origin (terrestrial, phytobenthos derived, and phytoplankton derived) of particulate OC (POC) and dissolved OC (DOC) in the water column and sedimentary OC using elemental, isotopic, and optical signatures in Furen Lagoon, Japan. Based on these data analysis, we explored how OC from multiple sources contributes to sequestration via storage in sediments, water column sequestration, and air–sea CO2 exchanges, and analyzed how the contributions vary with salinity in a shallow seagrass meadow as well. The relative contribution of terrestrial POC in the water column decreased with increasing salinity, whereas autochthonous POC increased in the salinity range 10–30. Phytoplankton-derived POC dominated the water column POC (65–95%) within this salinity range; however, it was minor in the sediments (3–29%). In contrast, terrestrial and phytobenthos-derived POC were relatively minor contributors in the water column but were major contributors in the sediments (49–78% and 19–36%, respectively), indicating that terrestrial and phytobenthos-derived POC were selectively stored in the sediments. Autochthonous DOC, part of which can contribute to long-term carbon sequestration in the water column, accounted for >25% of the total water column DOC pool in the salinity range 15–30. Autochthonous OC production decreased the concentration of dissolved inorganic carbon in the water column and thereby contributed to atmospheric CO2 uptake, except in the low-salinity zone. Our results indicate that shallow coastal ecosystems function not only as transition zones between land and ocean but also as carbon sequestration filters. They function at different timescales, depending on the salinity, and OC sources. PMID:25880367

Antarctic Ocean Nutrient Conditions During the Last Two Glacial Cycles

NASA Astrophysics Data System (ADS)

Studer, A.; Sigman, D. M.; Martinez-Garcia, A.; Benz, V.; Winckler, G.; Kuhn, G.; Esper, O.; Lamy, F.; Jaccard, S.; Wacker, L.; Oleynik, S.; Gersonde, R.; Haug, G. H.

2014-12-01

The high concentration of the major nutrients nitrate and phosphate in the Antarctic Zone of the Southern Ocean dictates the nature of Southern Ocean ecosystems and permits these nutrients to be carried from the deep ocean into the nutrient-limited low latitudes. Incomplete nutrient consumption in the Antarctic also allows the leakage of deeply sequestered carbon dioxide (CO2) back to the atmosphere, and changes in this leakage may have driven glacial/interglacial cycles in atmospheric CO2. In a sediment core from the Pacific sector of the Antarctic Ocean, we report diatom-bound N isotope (δ15Ndb) records for total recoverable diatoms and two assemblages of diatom species. These data indicate tight coupling between the degree of nitrate consumption and Antarctic climate across the last two glacial cycles, with δ15Ndb (and thus the degree of nitrate consumption) increasing at each major Antarctic cooling event. Measurements in the same sediment core indicate that export production was reduced during ice ages, pointing to an ice age reduction in the supply of deep ocean-sourced nitrate to the Antarctic Ocean surface. The reduced export production of peak ice ages also implies a weaker winter-to-summer decline (i.e. reduced seasonality) in mixed layer nitrate concentration, providing a plausible explanation for an observed reduction in the inter-assemblage δ15Ndb difference during these coldest times. Despite the weak summertime productivity, the reduction in wintertime nitrate supply from deep waters left the Antarctic mixed layer with a low nitrate concentration, and this wintertime change also would have reduced the outgassing of CO2. Relief of light limitation fails to explain the intermediate degree of nitrate consumption that characterizes early glacial conditions, as improved light limitation coincident with reduced nitrate supply would drive nitrate consumption to completion. Thus, the data favor iron availability as the dominant control on annual Antarctic Ocean export production over glacial cycles.

Plastid-bearing sea slugs fix CO2 in the light but do not require photosynthesis to survive

PubMed Central

Christa, Gregor; Zimorski, Verena; Woehle, Christian; Tielens, Aloysius G. M.; Wägele, Heike; Martin, William F.; Gould, Sven B.

2014-01-01

Several sacoglossan sea slugs (Plakobranchoidea) feed upon plastids of large unicellular algae. Four species—called long-term retention (LtR) species—are known to sequester ingested plastids within specialized cells of the digestive gland. There, the stolen plastids (kleptoplasts) remain photosynthetically active for several months, during which time LtR species can survive without additional food uptake. Kleptoplast longevity has long been puzzling, because the slugs do not sequester algal nuclei that could support photosystem maintenance. It is widely assumed that the slugs survive starvation by means of kleptoplast photosynthesis, yet direct evidence to support that view is lacking. We show that two LtR plakobranchids, Elysia timida and Plakobranchus ocellatus, incorporate 14CO2 into acid-stable products 60- and 64-fold more rapidly in the light than in the dark, respectively. Despite this light-dependent CO2 fixation ability, light is, surprisingly, not essential for the slugs to survive starvation. LtR animals survived several months of starvation (i) in complete darkness and (ii) in the light in the presence of the photosynthesis inhibitor monolinuron, all while not losing weight faster than the control animals. Contrary to current views, sacoglossan kleptoplasts seem to be slowly digested food reserves, not a source of solar power. PMID:24258718

Above Ground Carbon Stock Estimates of Mangrove Forest Using Worldview-2 Imagery in Teluk Benoa, Bali

NASA Astrophysics Data System (ADS)

Candra, E. D.; Hartono; Wicaksono, P.

2016-11-01

Mangrove forests have a role as an absorbent and a carbon sink to a reduction CO2 in the atmosphere. Based on the previous studies found that mangrove forests have the ability to sequestering carbon through photosynthesis and carbon burial of sediment effectively. The value and distribution of carbon stock are important to understand through remote sensing technology. In this study, will estimate the carbon stock using WorldView-2 imagery with and without distinction mangrove species. Worldview-2 is a high resolution image with 2 meters spatial resolution and eight spectral bands. Worldview-2 potential to estimate carbon stock in detail. Vegetation indices such as DVI (Difference Vegetation Index), EVI (Enhanced Vegetation Index), and MRE-SR (Modified Red Edge-Simple Ratio) and field data were modeled to determine the best vegetation indices to estimate carbon stocks. Carbon stock estimated by allometric equation approach specific to each species of mangrove. Worldview-2 imagery to map mangrove species with an accuracy of 80.95%. Total carbon stock estimation results in the study area of 35.349,87 tons of dominant species Rhizophora apiculata, Rhizophora mucronata and Sonneratia alba.

Applications of Satellite Geodesy in Environmental and Climate Change

NASA Astrophysics Data System (ADS)

Yang, Qian

Satellite geodesy plays an important role in earth observation. This dissertation presents three applications of satellite geodesy in environmental and climate change. Three satellite geodesy techniques are used: high-precision Global Positioning System (GPS), the Gravity Recovery and Climate Experiment (GRACE) and Interferometric Synthetic Aperture Radar (InSAR). In the first study, I use coastal uplift observed by GPS to study the annual changes in mass loss of the Greenland ice sheet. The data show both spatial and temporal variations of coastal ice mass loss and suggest that a combination of warm atmospheric and oceanic condition drove these variations. In the second study, I use GRACE monthly gravity change estimates to constrain recent freshwater flux from Greenland. The data show that Arctic freshwater flux started to increase rapidly in the mid-late 1990s, coincident with a decrease in the formation of dense Labrador Sea Water, a key component of the deep southward return flow od the Atlantic Meridional Overturning Circulation (AMOC). Recent freshening of the polar oceans may be reducing formation of Labrador Sea Water and hence may be weakening the AMOC. In the third study, I use InSAR to monitor ground deformation caused by CO2 injection at an enhanced oil recovery site in west Texas. Carbon capture and storage can reduce CO 2 emitted from power plants, and is a promising way to mitigate anthropogenic warming. From 2007 to 2011, ~24 million tons of CO2 were sequestered in this field, causing up to 10 MPa pressure buildup in a reservoir at depth, and surface uplift up to 10 cm. This study suggests that surface displacement observed by InSAR is a cost-effective way to estimate reservoir pressure change and monitor the fate of injected fluids at waste disposal and CO2 injection sites.

North Atlantic Deep Water Production during the Last Glacial Maximum

PubMed Central

Howe, Jacob N. W.; Piotrowski, Alexander M.; Noble, Taryn L.; Mulitza, Stefan; Chiessi, Cristiano M.; Bayon, Germain

2016-01-01

Changes in deep ocean ventilation are commonly invoked as the primary cause of lower glacial atmospheric CO2. The water mass structure of the glacial deep Atlantic Ocean and the mechanism by which it may have sequestered carbon remain elusive. Here we present neodymium isotope measurements from cores throughout the Atlantic that reveal glacial–interglacial changes in water mass distributions. These results demonstrate the sustained production of North Atlantic Deep Water under glacial conditions, indicating that southern-sourced waters were not as spatially extensive during the Last Glacial Maximum as previously believed. We demonstrate that the depleted glacial δ13C values in the deep Atlantic Ocean cannot be explained solely by water mass source changes. A greater amount of respired carbon, therefore, must have been stored in the abyssal Atlantic during the Last Glacial Maximum. We infer that this was achieved by a sluggish deep overturning cell, comprised of well-mixed northern- and southern-sourced waters. PMID:27256826

Deciphering ocean carbon in a changing world

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

Moran, Mary Ann; Kujawinski, Elizabeth B.; Stubbins, Aron

Dissolved organic matter (DOM) in the oceans is one of the largest pools of reduced carbon on Earth, comparable in size to the atmospheric CO 2 reservoir. The cycling of DOM over short and long time scales has profound impacts on the quantity of carbon sequestered in the oceans and the foundations of the food webs that support ocean life. At the heart of this cycle lie molecular-level relationships between the individual molecules in DOM and the members of the ocean microbiome that produce and consume them. In the past, these connections have defied clear definition and study because bothmore » DOM and microbial communities consist of many thousands of individual components. Emerging tools in analytical chemistry, microbiology and informatics are breaking down the barriers to a fuller appreciation of these connections. Furthermore, we highlight questions that are being addressed using this new toolkit and consider how these advances are transforming our understanding of some of the most important reactions of the marine carbon cycle.« less

Modern deposition rates and patterns of organic carbon burial in Fiordland, New Zealand

NASA Astrophysics Data System (ADS)

Ramirez, Michael T.; Allison, Mead A.; Bianchi, Thomas S.; Cui, Xingqian; Savage, Candida; Schüller, Susanne E.; Smith, Richard W.; Vetter, Lael

2016-11-01

Fjords are disproportionately important for global organic carbon (OC) burial relative to their spatial extent and may be important in sequestering atmospheric CO2, providing a negative climate feedback. Within fjords, multiple locally variable delivery mechanisms control mineral sediment deposition, which in turn modulates OC burial. Sediment and OC sources in Fiordland, New Zealand, include terrigenous input at fjord heads, sediment reworking over fjord-mouth sills, and landslide events from steep fjord walls. Box cores were analyzed for sedimentary texture, sediment accumulation rate, and OC content to evaluate the relative importance of each delivery mechanism. Sediment accumulation was up to 3.4 mm/yr in proximal and distal fjord areas, with lower rates in medial reaches. X-radiograph and 210Pb stratigraphy indicate mass wasting and surface-sediment bioturbation throughout the fjords. Sediment accumulation rates are inversely correlated with %OC. Spatial heterogeneity in sediment depositional processes and rates is important when evaluating OC burial within fjords.

Deciphering ocean carbon in a changing world

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

Moran, Mary Ann; Kujawinski, Elizabeth B.; Stubbins, Aron

2016-03-07

Dissolved organic matter (DOM) in the oceans is one of the largest pools of reduced carbon on Earth, comparable in size to the atmospheric CO2 reservoir. The cycling of DOM over short and long time scales has profound impacts on the quantity of carbon sequestered in the oceans and the foundations of the food webs that support ocean life. At the heart of this cycle lie molecular-level relationships between the individual molecules in DOM and the members of the ocean microbiome that produce and consume them. In the past, these connections have defied clear definition and study because both DOMmore » and microbial communities consist of many thousands of individual components. Emerging tools in analytical chemistry, microbiology and informatics are breaking down the barriers to a fuller appreciation of these connections. Here we highlight questions that are being addressed using this new toolkit and consider how these advances are transforming our understanding of some of the most important reactions of the marine carbon cycle.« less

Sulphur shuttling across a chaperone during molybdenum cofactor maturation.

PubMed

Arnoux, Pascal; Ruppelt, Christian; Oudouhou, Flore; Lavergne, Jérôme; Siponen, Marina I; Toci, René; Mendel, Ralf R; Bittner, Florian; Pignol, David; Magalon, Axel; Walburger, Anne

2015-02-04

Formate dehydrogenases (FDHs) are of interest as they are natural catalysts that sequester atmospheric CO2, generating reduced carbon compounds with possible uses as fuel. FDHs activity in Escherichia coli strictly requires the sulphurtransferase EcFdhD, which likely transfers sulphur from IscS to the molybdenum cofactor (Mo-bisPGD) of FDHs. Here we show that EcFdhD binds Mo-bisPGD in vivo and has submicromolar affinity for GDP-used as a surrogate of the molybdenum cofactor's nucleotide moieties. The crystal structure of EcFdhD in complex with GDP shows two symmetrical binding sites located on the same face of the dimer. These binding sites are connected via a tunnel-like cavity to the opposite face of the dimer where two dynamic loops, each harbouring two functionally important cysteine residues, are present. On the basis of structure-guided mutagenesis, we propose a model for the sulphuration mechanism of Mo-bisPGD where the sulphur atom shuttles across the chaperone dimer.

Deciphering ocean carbon in a changing world

DOE PAGES

Moran, Mary Ann; Kujawinski, Elizabeth B.; Stubbins, Aron; ...

2016-03-07

Dissolved organic matter (DOM) in the oceans is one of the largest pools of reduced carbon on Earth, comparable in size to the atmospheric CO 2 reservoir. The cycling of DOM over short and long time scales has profound impacts on the quantity of carbon sequestered in the oceans and the foundations of the food webs that support ocean life. At the heart of this cycle lie molecular-level relationships between the individual molecules in DOM and the members of the ocean microbiome that produce and consume them. In the past, these connections have defied clear definition and study because bothmore » DOM and microbial communities consist of many thousands of individual components. Emerging tools in analytical chemistry, microbiology and informatics are breaking down the barriers to a fuller appreciation of these connections. Furthermore, we highlight questions that are being addressed using this new toolkit and consider how these advances are transforming our understanding of some of the most important reactions of the marine carbon cycle.« less

Organic carbon sequestration under selected land use in Padang city, West Sumatra, Indonesia

NASA Astrophysics Data System (ADS)

Yulnafatmawita; Yasin, S.

2018-03-01

Organic carbon is a potential element to build biomass as well as emitting CO2 to the atmosphere and promotes global warming. This research was aimed to calculate the sequestered Carbon (C) within a 1-m soil depth under selected land use from 6 different sites in Padang city, Indonesia. Disturbed and undisturbed soil samples were taken from several horizons until 100 cm depth at each location. Soil parameters observed were organic carbon (OC), bulk density (BD), and soil texture. The result showed that soil OC content tended to decrease by the depth at all land use types, except under rice field in Kurao-Nanggalo which extremely increased at >65 cm soil depth with the highest carbon stock. The soil organic carbon sequestration from the highest to the lowest according to land use and the location is in the following order mix garden- Kayu Aro > mix garden- Aie Pacah > Rangeland- Parak Laweh >seasonal farming- Teluk Sirih > rice field- Kampuang Jua.

Pore Structure Characterization in Concrete Prepared with Carbonated Fly Ash

NASA Astrophysics Data System (ADS)

Sahoo, Sanjukta

2018-03-01

Carbon dioxide capture and storage (CCS) is a technique to address the global concern of continuously rising CO2 level in the atmosphere. Fly ash is considered as a suitable medium for CCS due to presence of metal oxides. The fly ash which has already sequestered carbon dioxide is referred to as carbonated fly ash. Recent research reveals better durability of concretes using carbonated fly ash as part replacement of cement. In the present research pore structure characterization of the carbonated fly ash concrete has been carried out. Mercury Intrusion porosimetry test has been conducted on control concrete and concrete specimens using fly ash and carbonated fly ash at replacement levels of 25% and 40%. The specimens have been water cured for 28 days and 90 days. It is observed that porosity reduction rate is more pronounced in carbonated fly ash concrete compared to control concrete at higher water curing age. Correlation analysis is also carried out which indicates moderately linear relationship between porosity % and pore distribution with particle size and water curing.

Sulphur shuttling across a chaperone during molybdenum cofactor maturation

NASA Astrophysics Data System (ADS)

Arnoux, Pascal; Ruppelt, Christian; Oudouhou, Flore; Lavergne, Jérôme; Siponen, Marina I.; Toci, René; Mendel, Ralf R.; Bittner, Florian; Pignol, David; Magalon, Axel; Walburger, Anne

2015-02-01

Formate dehydrogenases (FDHs) are of interest as they are natural catalysts that sequester atmospheric CO2, generating reduced carbon compounds with possible uses as fuel. FDHs activity in Escherichia coli strictly requires the sulphurtransferase EcFdhD, which likely transfers sulphur from IscS to the molybdenum cofactor (Mo-bisPGD) of FDHs. Here we show that EcFdhD binds Mo-bisPGD in vivo and has submicromolar affinity for GDP—used as a surrogate of the molybdenum cofactor’s nucleotide moieties. The crystal structure of EcFdhD in complex with GDP shows two symmetrical binding sites located on the same face of the dimer. These binding sites are connected via a tunnel-like cavity to the opposite face of the dimer where two dynamic loops, each harbouring two functionally important cysteine residues, are present. On the basis of structure-guided mutagenesis, we propose a model for the sulphuration mechanism of Mo-bisPGD where the sulphur atom shuttles across the chaperone dimer.

Influence of sustainable irrigation regimes and agricultural practices on the soil CO2 fluxes from olive groves in SE Spain

NASA Astrophysics Data System (ADS)

Marañón-Jiménez, Sara; Serrano-Ortíz, Penelope; Vicente-Vicente, Jose Luis; Chamizo, Sonia; Kowalski, Andrew S.

2017-04-01

Olive (Olea europaea) is the dominant agriculture plantation in Spain and its main product, olive oil, is vital to the economy of Mediterranean countries. Given the extensive surface dedicated to olive plantations, olive groves can potentially sequester large amounts of carbon and contribute to mitigate climate change. Their potential for carbon sequestration will, however, largely depend on the management and irrigation practices in the olive grove. Although soil respiration is the main path of C release from the terrestrial ecosystems to the atmosphere and a suitable indicator of soil health and fertility, the interaction of agricultural management practices with irrigation regimes on soil CO2 fluxes have not been assessed yet. Here we investigate the influence of the presence of herbaceous cover, use of artificial fertilizers and their interaction with the irrigation regime on the CO2 emission from the soil to the atmosphere. For this, the three agricultural management treatments were established in replicated plots in an olive grove in the SE of Spain: presence of herbaceous cover ("H"), exclusion of herbaceous cover by using herbicides ("NH"), and exclusion of herbaceous cover along with addition of artificial fertilizers (0.55 kg m-2 year-1 of N, P, K solid fertilizer in the proportion 20:10:10, "NHF"). Within each management treatment, three irrigation regimes were also implemented in a randomized design: no-irrigation ("NO") or rain fed, full irrigation (224 l week-1 per olive tree, "MAX"), and a 50% restriction (112 l week-1 per olive tree, "MED"). Soil respiration was measured every 2-3 weeks at 1, 3, and 5 meters from each olive tree together with soil temperature and soil moisture in order to account for the spatial and seasonal variability over the year. Soil respiration was higher when herbaceous cover was present compared to the herbaceous exclusion, whereas the addition of fertilizer did not exert any significant effect. Although the different irrigation regimes did affect soil moisture, soil CO2 fluxes remained unaffected by the amount of water added. Soil moisture and temperature were actually reduced by the presence of herbaceous cover during the growing season, which suggests water competition between herbaceous plants and olives with counteracting effects on soil respiration values. Soil respiration showed high spatial heterogeneity, with values decreasing exponentially with the distance from the olive trees. These data highlight the need to account for their spatial and seasonal heterogeneity when estimating the contribution of soil respiration to atmospheric CO2 emissions and the crucial role of the agricultural management on determining the carbon sequestration potential of soil from olive groves.

Diffusion-based process for carbon dioxide uptake and isoprene emission in gaseous/aqueous two-phase photobioreactors by photosynthetic microorganisms.

PubMed

Bentley, Fiona K; Melis, Anastasios

2012-01-01

Photosynthesis for the generation of fuels and chemicals from cyanobacteria and microalgae offers the promise of a single host organism acting both as photocatalyst and processor, performing sunlight absorption and utilization, as well as CO(2) assimilation and conversion into product. However, there is a need to develop methods for generating, sequestering, and trapping such bio-products in an efficient and cost-effective manner that is suitable for industrial scale-up and exploitation. A sealed gaseous/aqueous two-phase photobioreactor was designed and applied for the photosynthetic generation of volatile isoprene (C(5)H(8)) hydrocarbons, which operates on the principle of spontaneous diffusion of CO(2) from the gaseous headspace into the microalgal or cyanobacterial-containing aqueous phase, followed by photosynthetic CO(2) assimilation and isoprene production by the transgenic microorganisms. Volatile isoprene hydrocarbons were emitted from the aqueous phase and were sequestered into the gaseous headspace. Periodic replacement (flushing) of the isoprene (C(5)H(8)) and oxygen (O(2)) content of the gaseous headspace with CO(2) allowed for the simultaneous harvesting of the photoproducts and replenishment of the CO(2) supply in the gaseous headspace. Reduction in practice of the gaseous/aqueous two-phase photobioreactor is offered in this work with a fed-batch and a semi-continuous culturing system using Synechocystis sp. PCC 6803 heterologously expressing the Pueraria montana (kudzu) isoprene synthase (IspS) gene. Constitutive isoprene production was observed over 192 h of experimentation, coupled with cyanobacterial biomass accumulation. The diffusion-based process in gaseous/aqueous two-phase photobioreactors has the potential to be applied to other high-value photosynthetically derived volatile molecules, emanating from a variety of photosynthetic microorganisms. Copyright © 2011 Wiley Periodicals, Inc.

Potential fate of eroded SOC after erosion

NASA Astrophysics Data System (ADS)

Xiao, Liangang; Fister, Wolfgang; Greenwood, Philip; Hu, Yaxian; Kuhn, Nikolaus J.

2015-04-01

Globally, soils contain more than three times as much carbon as either atmosphere or terrestrial vegetation. Soil erosion moves soil organic carbon (SOC) from the site of soil and SOC formation and to depositional environments. There some SOC might be sequestered. Combined with dynamic replacement at the site of erosion, the effect can significantly influence the carbon cycle. However, the fate of SOC moved by erosion has been subject to an intense controversy. Two opposing views prevail: erosion may contribute to SOC mineralization during transport and thus act as a source for atmospheric CO2; the burial of SOC, on the other hand, can be seen as a sink while dynamic replacement maintains SOC at the eroding site and thus increase the C-stocks in soils and sediments. The debate suffers from a lack of information on the distribution, movement and fate of SOC in terrestrial ecosystems. This study aims to improve our understanding of the transport and subsequent fate of the eroded soil and the associated SOC. The research presented here focused on the SOC content and potential transport distance of erode soil. During a series of simulated rainfall soil eroded on crusted loess soils near Basel, Switzerland, was collected. The sediment was fractionated according to its settling velocity, with classes set to correspond to either a transfer into rivers or a deposition on slopes. The soil mass, SOC concentration and cumulative CO2 emission of each fraction were measured. Our results show that about 50% of the eroded sediment and 60% of the eroded SOC are likely to be deposited on the slopes, even during a high rainfall intensity event. This is 3 times greater than the association of SOC with mineral particles suggests. The CO2 emission of the eroded soil is increased by 40% compared to disturbed bulk soil. This confirms that aggregate breakdown reduces the protection of SOC in aggregates. Both results of this study show that taking (i) the effect of aggregation on SOC redistribution and (ii) the subsequent CO2 emission during the transport have to be considered to achieve a reliable assessment of the effect of soil erosion on the global C-cycle. They also indicate that our current balances may underestimate the CO2 emission caused by soil erosion.

Origin of carbon released from ecosystems affected by permafrost degradation in Northern Siberia

NASA Astrophysics Data System (ADS)

Gandois, L.; Hoyt, A.; Xu, X.; Hatte, C.; Teisserenc, R.; Tananaev, N.

2016-12-01

Permafrost soils and peatlands store half of the soil organic carbon stock worldwide, and are rapidly evolving as a result of permafrost thaw. Determining the origin (permafrost or recent photosynthesis) of carbon which is released to surface waters and the atmosphere is crucial to assess Arctic ecosystems' potential feedback to climate change. In order to evaluate it, we investigated the stable and radioactive content of carbon in solid organic matter, dissolved organic matter (DOM) and dissolved CO2 and CH4 in a discontinuous permafrost area of Siberia affected by permafrost degradation (Igarka, Graviyka catchment (67°27'11''N, 86°32'07''E)). We collected samples from the active layer, permafrost, surface water and bubbles from thermokarst lakes. We further investigated DOM and dissolved CO2 and CH4 in porewater profiles, streams and the catchment outlet. In thermokarst lakes, DOM of surface water as well as CO2 and CH4 from bubbles from lake sediments predominantly originate from modern carbon. In two locations, CO2 and CH4 from bubbles have relatively low 14C contents, with ages greater than 700 yr BP, but still younger that what was previously reported in Eastern Siberia. In all samples the Δ14C of CH4 and CO2 were strongly correlated, with CH4 being consistently older than CO2, indicating strong interrelation between CO2 and CH4 cycles. In our study, permafrost influenced CO2 and CH4 is found in small ponds where palsa collapse and the resulting bank erosion has mobilized sequestered carbon. In peatland porewater, the Δ14C of DOM, CO2 and CH4 increases with depth (DOM: 1385 ±45 yr BP at 2m), indicating a contribution from Holocene peatlands affected by permafrost. In deep layers, CO2 reduction is the dominant pathway of CH4 production, whereas acetate fermentation dominates in thermokarst lakes. In summary, the majority of dissolved CO2 and CH4 analyzed from thermokarst lakes and degraded peatlands is modern and originates from recently fixed carbon. Additionally, the DOM exported in small streams draining peatlands is also modern. However, at the catchment scale, an additional contribution from deep groundwater or thawing permafrost results in an intermediate Δ14C of DOM (300-400 yr BP) at the outlet of the Graviyka River.

Influence of the biosphere and circulation on atmospheric CO2

NASA Astrophysics Data System (ADS)

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

2017-12-01

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

Electricity without carbon dioxide: Assessing the role of carbon capture and sequestration in United States electric markets

NASA Astrophysics Data System (ADS)

Johnson, Timothy Lawrence

2002-09-01

Stabilization of atmospheric greenhouse gas concentrations will likely require significant cuts in electric sector carbon dioxide (CO2) emissions. The ability to capture and sequester CO2 in a manner compatible with today's fossil-fuel based power generating infrastructure offers a potentially low-cost contribution to a larger climate change mitigation strategy. This thesis fills a niche between economy-wide studies of CO 2 abatement and plant-level control technology assessments by examining the contribution that carbon capture and sequestration (CCS) might make toward reducing US electric sector CO2 emissions. The assessment's thirty year perspective ensures that costs sunk in current infrastructure remain relevant and allows time for technological diffusion, but remains free of assumptions about the emergence of unidentified radical innovations. The extent to which CCS might lower CO2 mitigation costs will vary directly with the dispatch of carbon capture plants in actual power-generating systems, and will depend on both the retirement of vintage capacity and competition from abatement alternatives such as coal-to-gas fuel switching and renewable energy sources. This thesis therefore adopts a capacity planning and dispatch model to examine how the current distribution of generating units, natural gas prices, and other industry trends affect the cost of CO2 control via CCS in an actual US electric market. The analysis finds that plants with CO2 capture consistently provide significant reductions in base-load emissions at carbon prices near 100 $/tC, but do not offer an economical means of meeting peak demand unless CO2 reductions in excess of 80 percent are required. Various scenarios estimate the amount by which turn-over of the existing generating infrastructure and the severity of criteria pollutant constraints reduce mitigation costs. A look at CO2 sequestration in the seabed beneath the US Outer Continental Shelf (OCS) complements this model-driven assessment by considering issues of risk, geological storage capacity, and regulation. Extensive experience with offshore oil and gas operations suggests that the technical uncertainties associated with OCS sequestration are not large. The legality of seabed CO 2 disposal under US law and international environmental agreements, however, is ambiguous, and the OCS may be the first region where these regulatory regimes clash over CO2 sequestration.

Water Utility Lime Sludge Reuse – An Environmental Sorbent for Power Utilities

EPA Science Inventory

Lime sludge can be used as an environmental sorbent to remove sulfur dioxide (SO2) and acid gases, by the ultra-fine CaCO3 particles, and to sequester mercury and other heavy metals, by the Natural Organic Matter and residual activated carbon. The laboratory experimental set up ...

Chamber and Diffusive Based Carbon Flux Measurements in an Alaskan Arctic Ecosystem

NASA Astrophysics Data System (ADS)

Wilkman, E.; Oechel, W. C.; Zona, D.

2013-12-01

Eric Wilkman, Walter Oechel, Donatella Zona Comprising an area of more than 7 x 106 km2 and containing over 11% of the world's organic matter pool, Arctic terrestrial ecosystems are vitally important components of the global carbon cycle, yet their structure and functioning are sensitive to subtle changes in climate and many of these functional changes can have large effects on the atmosphere and future climate regimes (Callaghan & Maxwell 1995, Chapin et al. 2002). Historically these northern ecosystems have acted as strong C sinks, sequestering large stores of atmospheric C due to photosynthetic dominance in the short summer season and low rates of decomposition throughout the rest of the year as a consequence of cold, nutrient poor, and generally water-logged conditions. Currently, much of this previously stored carbon is at risk of loss to the atmosphere due to accelerated soil organic matter decomposition in warmer future climates (Grogan & Chapin 2000). Although there have been numerous studies on Arctic carbon dynamics, much of the previous soil flux work has been done at limited time intervals, due to both the harshness of the environment and labor and time constraints. Therefore, in June of 2013 an Ultraportable Greenhouse Gas Analyzer (UGGA - Los Gatos Research Inc.) was deployed in concert with the LI-8100A Automated Soil Flux System (LI-COR Biosciences) in Barrow, AK to gather high temporal frequency soil CO2 and CH4 fluxes from a wet sedge tundra ecosystem. An additional UGGA in combination with diffusive probes, installed in the same location, provides year-round soil and snow CO2 and CH4 concentrations. When used in combination with the recently purchased AlphaGUARD portable radon monitor (Saphymo GmbH), continuous soil and snow diffusivities and fluxes of CO2 and CH4 can be calculated (Lehmann & Lehmann 2000). Of particular note, measuring soil gas concentration over a diffusive gradient in this way allows one to separate both net production and consumption, whereas chamber and eddy covariance methodologies only document net production from the surface. Also, the capability to measure spring, summer and fall chamber fluxes, and to continuously determine year-round CO2 and CH4 fluxes under even the most extreme weather conditions, allows an unprecedented level of data continuity and local spatial coverage. Comparison to a nearby eddy covariance tower measuring CO2 and CH4 fluxes with an LGR Fast Greenhouse Gas Analyzer add additional power to this set of measurements. Thus, inter-comparison between diffusive, chamber, and tower-based carbon fluxes should lend much insight into the spatial and temporal controls on carbon cycling in this ecosystem.

Subsidence in tropical peatlands: Estimating CO2 fluxes from peatlands in Southeast Asia

NASA Astrophysics Data System (ADS)

Hoyt, A.; Harvey, C. F.; Seppalainen, S. S.; Chaussard, E.

2017-12-01

Tropical peatlands of Southeast Asia are an important global carbon stock. However, they are being rapidly deforested and drained. Peatland drainage facilitates peat decomposition, releases sequestered peat carbon to the atmosphere as CO2, and leads to subsidence of the peat surface. As a result, subsidence measurements can be used to monitor peatland carbon loss over time. Until now, subsidence measurements have been primarily limited to ground-based point measurements using subsidence poles. Here we demonstrate a powerful method to measure peatland subsidence rates across much larger areas than ever before. Using remotely sensed InSAR data, we map subsidence rates across thousands of square kilometers in Southeast Asia and validate our results against ground-based subsidence measurements. The method allows us to monitor subsidence in remote locations, providing unprecedented spatial information, and the first comprehensive survey of land uses such as degraded peatlands, burnt and open areas, shrub lands, and smallholder farmlands. Strong spatial patterns emerged, with the highest subsidence rates occurring at the centers of peat domes, where the peat is thickest and drainage depths are likely to be largest. Peatland subsidence rates were also strongly dependent on current and historical land use, with typical subsidence rates ranging from 2-4 cm/yr. Finally, we scaled up our results to calculate total annual emissions from peat decomposition in degraded peatlands.

Tectono-thermal History of the Southern Nenana Basin, Interior Alaska: Implications for Conventional and Unconventional Hydrocarbon Exploration

NASA Astrophysics Data System (ADS)

Dixit, N. C.; Hanks, C. L.

2014-12-01

The Tertiary Nenana basin of Interior Alaska is currently the focus of both new oil exploration and coalbed methane exploitation and is being evaluated as a potential CO2sequestration site. The basin first formed as a Late Paleocene extensional rift with the deposition of oil and gas-prone, coal-bearing non-marine sediments with excellent source potential. Basin inversion during the Early Eocene-Early Oligocene times resulted in folding and erosion of higher stratigraphic levels, forming excellent structural and stratigraphic traps. Initiation of active faulting on its eastern margin in the middle Oligocene caused slow tectonic subsidence that resulted in the deposition of reservoir and seal rocks of the Usibelli Group. Onset of rapid tectonic subsidence in Pliocene that continues to the present-day has provided significant pressure and temperature gradient for the source rocks. Apatite fission-track and vitrinite reflectance data reveals two major paleo-thermal episodes: Late Paleocene to Early Eocene (60 Ma to 54.8 Ma) and Late Miocene to present-day (7 Ma to present). These episodes of maximum paleotemperatures have implications for the evolution of source rock maturity within the basin. In this study, we are also investigating the potential for coalbed methane production from the Late Paleocene coals via injection of CO2. Our preliminary analyses demonstrate that 150 MMSCF of methane could be produced while 33000 tonnes of CO2 per injection well (base case of ~9 years) can be sequestered in the vicinity of existing infrastructure. However, these volumes of sequestered CO2and coal bed methane recovery are estimates and are sensitive to the reservoir's geomechanical and flow properties. Keywords: extensional rift, seismic, subsidence, thermal history, fission track, vitrinite reflectance, coal bed methane, Nenana basin, CO2 sequestration

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

PubMed

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

2016-11-01

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

Natural Terrestrial Sequestration Potential of Highplains Prairie to Subalpine Forest and Mined-Lands Soils Derived from Weathering of Tertiary Volcanics

NASA Astrophysics Data System (ADS)

Yager, D. B.; Burchell, A.; Robinson, R.; Odell, S.; Dick, R. P.; Johnson, C. A.; Hidinger, J.; Rathke, D.

2007-12-01

There is now widespread agreement that, if the climate is to be stabilized, then net greenhouse gas emissions must be greatly reduced (IPCC, 2007). The need to reduce net CO2 emissions plus the possible economic and environmental ramifications of not addressing climate change have stimulated important atmospheric carbon mitigation actions, as well as, studies to understand and quantify potential carbon sinks. Soils represent a potentially large and environmentally significant natural carbon reservoir. Increasing the natural terrestrial sequestration potential (NTS) of soils is among the seven, "Sokolow CO2 stabilization wedges' or carbon management strategies needed to thwart doubling of atmospheric CO2. Additionally, high plains to subalpine temperate soils tend to be less susceptible to baseline C pool declines due to global warming than are warmer regions and are important ecosystems in which to quantify soil carbon storage capacity. To examine the potential of magnesium silicate-bearing soils to sequester additional carbon, we sampled 60 high plains prairie to subalpine forest soil horizons derived from weathering of Tertiary-age dacite-andesite- basalt compositions in Colorado, U.S.A.: the San Luis Valley, San Juan Volcanic Field, Grand Mesa, White River- Roan Plateau (Flat Tops), Rocky Mountain National Park, Front Range and propylitically-altered terrain in the western San Juan Volcanic field containing secondary magnesium silicates (chlorite-species). Data for C, N, O (total conc., isotopes), metals, major and trace elements, Hg, S, microbial enzymes (β-glucosidase, arylsulfatase, acid neutralizing capacity (ANC), and 14C radiocarbon dates are reported. Samples demonstrate variable but elevated C relative to average global soil C. In particular, the propylitically-altered rocks have a high instantaneous ANC in laboratory tests (> 20 kg/ton CaCO3 equivalent) and derivative forest soils containing low-temperature charcoal "burn" horizons have high total organic carbon contents (12-14 Wt.% in the A-B horizons; 0 to 30 cm). These data are important to understanding the carbon sequestration potential that soils derived from intermediate to mafic igneous rocks can provide. Additionally, for range or forest management and mine waste remediation scenarios, this data suggests C mitigation efforts may be augmented by 'geomimicry' scenarios whereby projects model and enhance natural processes that support CO2 sequestration.

Climatic Controls on Forest Productivity in Western North America; Variability, Covariability, and Projected Change

NASA Astrophysics Data System (ADS)

Hawkins, L. R.; Rupp, D. E.; Li, S.; Mote, P.; Sparrow, S.; Massey, N.

2016-12-01

The forests of western North America serve as a carbon sink sequestering carbon and slowing the rise of CO2 in the atmosphere. Though still positive, the rate of net carbon uptake has been in decline over the past two decades. Regional drought has been shown to slow forest productivity and net carbon uptake despite warmer temperatures and longer growing seasons. With drought conditions projected to increase in frequency and severity under climate change there is concern that these forests' capacity as an effective carbon sink will continue to decrease in the future. To investigate how changes in regional hydroclimate may affect future carbon uptake in western US forests we dynamically downscaled global climate simulations using a 25-km resolution regional climate model HadRM3P with the land surface scheme MOSES2. We generated a 100-member ensemble of simulations for an historical period (1985-2015) and mid-21st century period (2030-2060) under Representative Concentration Pathway 8.5. We evaluated the effects of regional changes in atmospheric moisture demand, seasonality of water supply, and water stress on forest productivity and carbon uptake. We investigated how these changes in hydroclimate interact with the relaxing of temperature controls. This work can inform future adaptation efforts through improving our understanding of climatic controls on forest carbon sequestration.

CO2 condensation is a serious limit to the deglaciation of Earth-like planets

NASA Astrophysics Data System (ADS)

Turbet, Martin; Forget, Francois; Leconte, Jeremy; Charnay, Benjamin; Tobie, Gabriel

2017-10-01

It is widely believed that the carbonate-silicate cycle is the main agent, through volcanism, to trigger deglaciations by CO2 greenhouse warming on Earth and on Earth-like planets when they get in a frozen state. Here we use a 3D Global Climate Model to simulate the ability of planets initially completely frozen to escape from glaciation episodes by accumulating enough gaseous CO2. The model includes CO2 condensation and sublimation processes and the water cycle. We find that planets with Earth-like characteristics (size, mass, obliquity, rotation rate, etc.) orbiting a Sun-like star may never be able to escape from a glaciation era, if their orbital distance is greater than ∼1.27 Astronomical Units (Flux < 847 Wm-2 or 62% of the Solar constant), because CO2 would condense at the poles - here the cold traps - forming permanent CO2 ice caps. This limits the amount of CO2 in the atmosphere and thus its greenhouse effect. Furthermore, our results indicate that for (1) high rotation rates (Prot < 24 h), (2) low obliquity (obliquity <23.5°), (3) low background gas partial pressures (<1 bar), and (4) high water ice albedo (H2O albedo > 0.6), this critical limit could occur at a significantly lower equivalent distance (or higher insolation). For each possible configuration, we show that the amount of CO2 that can be trapped in the polar caps depends on the efficiency of CO2 ice to flow laterally as well as its gravitational stability relative to subsurface water ice. We find that a frozen Earth-like planet located at 1.30 AU of a Sun-like star could store as much as 1.5, 4.5 and 15 bars of dry ice at the poles, for internal heat fluxes of 100, 30 and 10 mW m-2, respectively. But these amounts are in fact lower limits. For planets with a significant water ice cover, we show that CO2 ice deposits should be gravitationally unstable. They get buried beneath the water ice cover in geologically short timescales of ∼104 yrs, mainly controlled by the viscosity of water ice. CO2 would be permanently sequestered underneath the water ice cover, in the form of CO2 liquids, CO2 clathrate hydrates and/or dissolved in subglacial water reservoirs (if any). This would considerably increase the amount of CO2 trapped and further reduce the probability of deglaciation.

Tree- Rings Link Climate and Carbon Storage in a Northern Mixed Hardwood Forest

NASA Astrophysics Data System (ADS)

Chiriboga, A.

2007-12-01

The terrestrial biosphere is a variable sink for atmospheric carbon dioxide. It is important to understand how carbon storage in trees is affected by natural climate variability to better characterize the sink. Quantifying the sensitivity of forest carbon storage to climate will improve carbon budgets and have implications for forest management practices. Here we explore how climate variability affects the ability of a northern mixed hardwood forest in Michigan to sequester atmospheric carbon dioxide in woody tissues. This site is ideal for studies of carbon sequestration; The University of Michigan Biological Station is an Ameriflux site, and has detailed meteorological and biometric records, as well as CO2 flux data. We have produced an 82- year aspen (Populus grandidentata) tree-ring chronology for this site, and measured ring widths at several heights up the bole. These measurements were used to estimate annual wood volume, which represents carbon allocated to aboveground carbon stores. Standard dendroclimatological techniques are used to identify environmental factors (e.g. temperature or precipitation) that drive tree-ring increment variability in the past century, and therefore annual carbon storage in this forest. Preliminary results show that marker years within the tree- ring chronology correspond with years that have cold spring temperatures. This suggests that trees at this site are temperature sensitive.

Do Titan's Mountains Betray the Late Acquisition of its Current Atmosphere

NASA Technical Reports Server (NTRS)

Moore, Jeffrey Morgan; Nimmo, F.

2011-01-01

Titan may have acquired its massive atmosphere relatively recently in solar system history [1,2,3,4]. Prior to that time, Titan would have been nearly airless, with its volatiles frozen or sequestered. Present-day Titan experiences only small (approximately 4 K) pole-to-equator variations, owing to efficient heat transport via the thick atmosphere [5]; these temperature variations would have been much larger (approximately 20 K) in the absence of an atmosphere. If Titan's ice shell is conductive, the change in surface temperature associated with the development of an atmosphere would have led to changes in shell thickness. In particular, the poles would move down (inducing compression) while the equator would move up. Figure 1 shows the predicted change in surface elevation as a result of the change in surface temperature, using the numerical conductive shell thickness model of [6

Effects of urban tree management and species selection on atmospheric carbon dioxide

Treesearch

David J. Nowak; Jack C. Stevens; Susan M. Sisinni; Christopher J. Luley

2002-01-01

Trees sequester and store carbon in their tissue at differing rates and amounts based on such factors as tree size at maturity, life span, and growth rate. Concurrently, tree care practices release carbon back to the atmosphere based on fossil-fuel emissions from maintenance equipment (e.g., chain saws, trucks, chippers). Management choices such as tree locations for...

In-Situ MVA of CO 2 Sequestration Using Smart Field Technology

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

Mohaghegh, Shahab D.

2014-09-01

Capability of underground carbon dioxide storage to confine and sustain injected CO 2 for a long period of time is the main concern for geologic CO 2 sequestration. If a leakage from a geological CO 2 sequestration site occurs, it is crucial to find the approximate amount and the location of the leak, in a timely manner, in order to implement proper remediation activities. An overwhelming majority of research and development for storage site monitoring has been concentrated on atmospheric, surface or near surface monitoring of the sequestered CO 2 . This study aims to monitor themore » integrity of CO 2 storage at the reservoir level. This work proposes developing in-situ CO 2 Monitoring and Verification technology based on the implementation of Permanent Down-hole Gauges (PDG) or “Smart Wells” along with Artificial Intelligence and Data Mining (AI&DM). The technology attempts to identify the characteristics of the CO 2 leakage by de-convolving the pressure signals collected from Permanent Down-hole Gauges (PDG). Citronelle field, a saline aquifer reservoir, located in the U.S. was considered as the basis for this study. A reservoir simulation model for CO 2 sequestration in the Citronelle field was developed and history matched. PDGs were installed, and therefore were considered in the numerical model, at the injection well and an observation well. Upon completion of the history matching process, high frequency pressure data from PDGs were generated using the history matched numerical model using different CO 2 leakage scenarios. Since pressure signal behaviors were too complicated to de-convolute using any existing mathematical formulations, a Machine Learning-based technology was introduced for this purpose. An Intelligent Leakage Detection System (ILDS) was developed as the result of this effort using the machine learning and pattern recognition technologies. The ILDS is able to detect leakage characteristics in a short period of time (less than a day from its occurrence) demonstrating the capability of the system in quantifying leakage characteristics subject to complex rate behaviors. The performance of ILDS is examined under different conditions such as multiple well leakages, cap rock leakage, availability of an additional monitoring well, presence of pressure drift and noise in the pressure sensor and uncertainty in the reservoir model.« less

A 3D Global Climate Model of the Pluto atmosphere coupled to a volatile transport model to interpret New Horizons observations, including the N2, CH4 and CO cycles and the formation of organic hazes

NASA Astrophysics Data System (ADS)

Bertrand, Tanguy; Forget, Francois

2016-04-01

To interpret New Horizons observations and simulate the Pluto climate system, we have developed a Global Climate Model (GCM) of Pluto's atmosphere. In addition to a 3D "dynamical core" which solves the equation of meteorology, the model takes into account the N2 condensation and sublimation and its thermal and dynamical effects, the vertical turbulent mixing, the radiative transfer through methane and carbon monoxide, molecular thermal conduction, and a detailed surface thermal model with different thermal inertia for various timescales (diurnal, seasonal). The GCM also includes a detailed model of the CH4 and CO cycles, taking into account their transport by the atmospheric circulation and turbulence, as well as their condensation and sublimation on the surface and in the atmosphere, possibly forming methane ice clouds. The GCM consistently predicts the 3D methane abundance in the atmosphere, which is used as an input for our radiative transfer calculation. In a second phase, we also developed a volatile transport model, derived from the GCM, which can be run over thousands of years in order to reach consistent initial states for the GCM runs and better explore the seasonal processes on Pluto. Results obtained with the volatile transport model show that the distribution of N2, CH4 and CO ices primarily depends on the seasonal thermal inertia used for the different ices, and is affected by the assumed topography as well. As observed, it is possible to form a large and permanent nitrogen glacier with CO and CH4 ice deposits in an equatorial basin corresponding to Sputnik Planum, while having a surface pressure evolution consistent with stellar occultations and New Horizons data. In addition, most of the methane ice is sequestered with N2 ice in the basin but seasonal polar caps of CH4 frosts also form explaining the bright polar caps observed with Hubble in the 1980s and in line with New Horizons observations. Using such balanced combination of surface and subsurface conditions as initial conditions, we run the GCM from 1975 to 2015, so that the model become insensitive to the assumed atmospheric initial states (that are not constrained by the volatile transport model). The simulated thermal structure and waves can be compared to the New Horizons occultations measurements. As observed, the horizontal variability is very limited, for fundamental reasons. In addition, we have developed a 3D model of the formation of organic hazes within the GCM. It includes the different steps of aerosols formation as understood on Titan: photolysis of CH4 in the upper atmosphere by the Lyman-alpha radiation, production of various gaseous precursor species, conversion into solid particles through chemistry and aggregation processes, and gravitational sedimentation. Significant amount of haze particles are found to be present at all latitudes up to 100 km. However, if N2 ice is already condensing in the polar night, the majority of the haze particles tend to accumulate in the polar night because of the transport of the haze precursors and aerosols by the condensation flow.

Growing Season Carbon Dioxide Exchange in Flooded Non-Mulching and Non-Flooded Mulching Cotton

PubMed Central

Li, Zhi-guo; Zhang, Run-hua; Wang, Xiu-jun; Chen, Fang; Tian, Chang-yan

2012-01-01

There is much interest in the role that agricultural practices might play in sequestering carbon to help offset rising atmospheric CO2 concentrations. However, limited information exists regarding the potential for increased carbon sequestration of different management strategies. The objective of this study was to quantify and contrast carbon dioxide exchange in traditional non-mulching with flooding irrigation (TF) and plastic film mulching with drip irrigation (PM) cotton (Gossypium hirsutum L.) fields in northwest China. Net primary productivity (NPP), soil heterotrophic respiration (R h) and net ecosystem productivity (NEP) were measured during the growing seasons in 2009 and 2010. As compared with TF, PM significantly increased the aboveground and belowground biomass and the NPP (340 g C m−2 season−1) of cotton, and decreased the R h (89 g C m−2 season−1) (p<0.05). In a growing season, PM had a higher carbon sequestration in terms of NEP of ∼ 429 g C m−2 season−1 than the TF. These results demonstrate that conversion of this type of land use to mulching practices is an effective way to increase carbon sequestration in the short term in cotton systems of arid areas. PMID:23226376

Robust CO2 Injection: Application of Bayesian-Information-Gap Decision Theory

NASA Astrophysics Data System (ADS)

Grasinger, M.; O'Malley, D.; Vesselinov, V. V.; Karra, S.

2015-12-01

Carbon capture and sequestration has the potential to reduce greenhouse gasemissions. However, care must be taken when choosing a site for CO2 seques-tration to ensure that the CO2 remains sequestered for many years, and thatthe environment is not harmed in any way. Making a rational decision be-tween potential sites for sequestration is not without its challenges because, asin the case of many environmental and subsurface problems, there is a lot ofuncertainty that exists. A method for making decisions under various typesand severities of uncertainty, Bayesian-Information-Gap Decision Theory (BIGDT), is presented. BIG DT was coupled with a numerical model for CO2 wellinjection and the resulting framework was then applied to a problem of selectingbetween two potential sites for CO2 sequestration. The results of the analysisare presented, followed by a discussion of the decision process.

Scoping Alternatives for Negative Emission Technologies. FRACCC - Possible Routes to Biomass-Derived Carbon Injection in Shallow Aquifers?

NASA Astrophysics Data System (ADS)

Correa Silva, R.; Larter, S.

2016-12-01

Atmospheric CO2 capture into biomass is one of the capture options for negative emission technologies, although proposed sequestration systems such as the permanent burial of total fresh biomass, algal lipids or soil amendment with biochar are yet to be successfully demonstrated as effective at scale. In the context of carbon sequestration, shallow geological reservoirs have not been exhaustively explored, even though they pose, away from groundwater protection zones, potentially low implementation cost, and geographically abundant potential carbon storage reservoirs. Typical carbon storage vectors considered, such as CO2 and biochar, are not suitable for shallow aquifer disposal, due either to cap rock containment requirements, or shallow aquifer CO2 densities, or issues related to formation damage from solid particles. Thus, a cost-effective technology, aimed at converting biomass into a large-scale carbon vector fit-for-disposal in shallow formations could be significant, linking promising carbon capture and containment strategies. In this work, we discuss the development of unconventional carbon vectors for subsurface storage in the form of Functionalized, Refractory and Aqueous Compatible Carbon Compounds (FRACCC), as a potential alternative negative emission technology (Larter et al., 2010). The concept is based on CO2 capture into microbial and algal biomass, followed by the modification of biomass constituents through facile chemical reactions aimed at rendering the biomass efficiently into a stable, biologically refractory but water soluble form, similar in some regards, to dissolved organic matter in the oceans, then sequestering the material in geological settings. As the injected material is not buoyant, containment specifications are more modest than for CO2 injection and potentially, more reservoirs could be accessible! This work analyses the technological, economic and societal implications of such potential FRACCC technologies, and make an assessment of whether such routes are likely to be technically, economically and politically viable.

Carbon sequestration index as a determinant for climate change mitigation: Case study of Bintan Island

NASA Astrophysics Data System (ADS)

Wahyudi, A.'an J.; Afdal; Prayudha, Bayu; Dharmawan, I. W. E.; Irawan, Andri; Abimanyu, Haznan; Meirinawati, Hanny; Surinati, Dewi; Syukri, Agus F.; Yuliana, Chitra I.; Yuniati, Putri I.

2018-02-01

The increase of the anthropogenic carbon dioxide (CO2) affects the global carbon cycle altering the atmospheric system and initiates the climate changes. There are two ways to mitigate these changes, by maintaining the greenhouse gasses below the carbon budget and by conserving the marine and terrestrial vegetation for carbon sequestration. These two strategies become variable to the carbon sequestration index (CSI) that represents the potential of a region in carbon sequestration, according to its natural capacity. As a study case, we conducted carbon sequestration research in Bintan region (Bintan Island and its surrounding), Riau Archipelago province. This research was aimed to assess the CSI and its possibility for climate change mitigation. We observed carbon sequestration of seagrass meadows and mangrove, greenhouse gas (CO2) emission (correlated to population growth, the increase of vehicles), and CSI. Bintan region has 125,849.9 ha of vegetation area and 14,879.6 ha of terrestrial and marine vegetation area, respectively. Both vegetation areas are able to sequester 0.262 Tg C yr-1 in total and marine vegetation contributes about 77.1%. Total CO2 emission in Bintan region is up to 0.273 Tg C yr-1, produced by transportation, industry and land use sectors. Therefore, CSI of the Bintan region is 0.98, which is above the global average (i.e. 0.58). This value demonstrates that the degree of sequestration is comparable to the total carbon emission. This result suggests that Bintan’s vegetation has high potential for reducing greenhouse gas effects.

A mechanistic understanding of plagioclase dissolution based on Al occupancy and T-O bond length: from geologic carbon sequestration to ambient conditions.

PubMed

Yang, Yi; Min, Yujia; Jun, Young-Shin

2013-11-14

A quantitative description of how the bulk properties of aluminosilicates affect their dissolution kinetics is important in helping people understand the regulation of atmospheric CO2 concentration by silicate weathering and predict the fate and transport of geologically sequestered CO2 through brine-rock interactions. In this study, we employed a structure model based on the C1 space group to illustrate how differences in crystallographic properties of aluminosilicates, such as T-O (Tetrahedral site-Oxygen) bond length and Al/Si ordering, can result in quantifiable variations in mineral dissolution rates. The dissolution rates of plagioclases were measured under representative geologic carbon sequestration (GCS) conditions (90 °C, 100 atm of CO2, 1.0 M NaCl, and pH ∼ 3.1), and used to validate the model. We found that the logarithm of the characteristic time of the breakdown of Al-O-Si linkages in plagioclases follows a good linear relation with the mineral's aluminum content (nAl). The Si release rates of plagioclases can be calculated based on an assumption of dissolution congruency or on the regularity of Al/Si distribution in the constituent tetrahedra of the mineral. We further extended the application of our approach to scenarios where dissolution incongruency arises because of different linkage reactivities in the solid matrix, and compared the model predictions with published data. The application of our results enables a significant reduction of experimental work for determining the dissolution rates of structurally related aluminosilicates, given a reaction environment.

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

PubMed

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

2011-03-01

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

Unearthing the hidden world of roots: Root biomass and architecture differ among species within the same guild

Treesearch

Katherine Sinacore; Jefferson Scott Hall; Catherine Potvin; Alejandro A. Royo; Mark J. Ducey; Mark S. Ashton; Shijo Joseph

2017-01-01

The potential benefits of planting trees have generated significant interest with respect to sequestering carbon and restoring other forest based ecosystem services. Reliable estimates of carbon stocks are pivotal for understanding the global carbon balance and for promoting initiatives to mitigate CO2 emissions through forest management. There...

How to estimate carbon sequestration on small forest tracts estimate carbon sequestration on small forest tracts

Treesearch

Coeli M. Hoover; Richard A. Birdsey; Linda S. Heath; Susan L. Stout

2000-01-01

International climate change agreements may allow carbon stored as a result of afforestation and reforestation to be used to offset CO2 emissions. Monitoring the carbon sequestered or released through forest management activities thus becomes important. Estimating forest carbon storage is feasible even for nonindustrial private forestland (NIPF)...

Atmospheric Collapse on Early Mars: The Role of CO2 Clouds

NASA Technical Reports Server (NTRS)

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

2017-01-01

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

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

NASA Astrophysics Data System (ADS)

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

2014-09-01

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

Insights into the structure of mixed CO 2/CH 4 in gas hydrates

DOE PAGES

Everett, S. Michelle; Rawn, Claudia J.; Chakoumakos, Bryan C.; ...

2015-05-12

The exchange of carbon dioxide for methane in natural gas hydrates is an attractive approach to harvesting CH 4 for energy production while simultaneously sequestering CO 2. In addition to the energy and environmental implications, the solid solution of clathrate hydrate (CH 4) 1-x(CO 2) x·5.75H 2O provides a model system to study how the distinct bonding and shapes of CH 4 and CO 2 influence the structure and properties of the compound. In this paper, high-resolution neutron diffraction was used to examine mixed CO 2/CH 4 gas hydrates. CO 2-rich hydrates had smaller lattice parameters, which were attributed tomore » the higher affinity of the CO 2 molecule interacting with H 2O molecules that form the surrounding cages, and resulted in a reduction in the unit-cell volume. Experimental nuclear scattering densities illustrate how the cage occupants and energy landscape change with composition. Finally, these results provide important insights on the impact and mechanisms for the structure of mixed CH 4/CO 2 gas hydrate.« less

Modeling and Evaluation of Geophysical Methods for Monitoring and Tracking CO2 Migration

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

Daniels, Jeff

2012-11-30

Geological sequestration has been proposed as a viable option for mitigating the vast amount of CO{sub 2} being released into the atmosphere daily. Test sites for CO{sub 2} injection have been appearing across the world to ascertain the feasibility of capturing and sequestering carbon dioxide. A major concern with full scale implementation is monitoring and verifying the permanence of injected CO{sub 2}. Geophysical methods, an exploration industry standard, are non-invasive imaging techniques that can be implemented to address that concern. Geophysical methods, seismic and electromagnetic, play a crucial role in monitoring the subsurface pre- and post-injection. Seismic techniques have beenmore » the most popular but electromagnetic methods are gaining interest. The primary goal of this project was to develop a new geophysical tool, a software program called GphyzCO2, to investigate the implementation of geophysical monitoring for detecting injected CO{sub 2} at test sites. The GphyzCO2 software consists of interconnected programs that encompass well logging, seismic, and electromagnetic methods. The software enables users to design and execute 3D surface-to-surface (conventional surface seismic) and borehole-to-borehole (cross-hole seismic and electromagnetic methods) numerical modeling surveys. The generalized flow of the program begins with building a complex 3D subsurface geological model, assigning properties to the models that mimic a potential CO{sub 2} injection site, numerically forward model a geophysical survey, and analyze the results. A test site located in Warren County, Ohio was selected as the test site for the full implementation of GphyzCO2. Specific interest was placed on a potential reservoir target, the Mount Simon Sandstone, and cap rock, the Eau Claire Formation. Analysis of the test site included well log data, physical property measurements (porosity), core sample resistivity measurements, calculating electrical permittivity values, seismic data collection, and seismic interpretation. The data was input into GphyzCO2 to demonstrate a full implementation of the software capabilities. Part of the implementation investigated the limits of using geophysical methods to monitor CO{sub 2} injection sites. The results show that cross-hole EM numerical surveys are limited to under 100 meter borehole separation. Those results were utilized in executing numerical EM surveys that contain hypothetical CO{sub 2} injections. The outcome of the forward modeling shows that EM methods can detect the presence of CO{sub 2}.« less

Renewal of Collaborative Research: Economically Viable Forest Harvesting Practices That Increase Carbon Sequestration

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

Davidson, E.A.; Dail, D.B., Hollinger, D.; Scott, N.

Forests provide wildlife habitat, water and air purification, climate moderation, and timber and nontimber products. Concern about climate change has put forests in the limelight as sinks of atmospheric carbon. The C stored in the global vegetation, mostly in forests, is nearly equivalent to the amount present in atmospheric CO{sub 2}. Both voluntary and government-mandated carbon trading markets are being developed and debated, some of which include C sequestration resulting from forest management as a possible tradeable commodity. However, uncertainties regarding sources of variation in sequestration rates, validation, and leakage remain significant challenges for devising strategies to include forest managementmore » in C markets. Hence, the need for scientifically-based information on C sequestration by forest management has never been greater. The consequences of forest management on the US carbon budget are large, because about two-thirds of the {approx}300 million hectare US forest resource is classified as 'commercial forest.' In most C accounting budgets, forest harvesting is usually considered to cause a net release of C from the terrestrial biosphere to the atmosphere. However, forest management practices could be designed to meet the multiple goals of providing wood and paper products, creating economic returns from natural resources, while sequestering C from the atmosphere. The shelterwood harvest strategy, which removes about 30% of the basal area of the overstory trees in each of three successive harvests spread out over thirty years as part of a stand rotation of 60-100 years, may improve net C sequestration compared to clear-cutting because: (1) the average C stored on the land surface over a rotation increases, (2) harvesting only overstory trees means that a larger fraction of the harvested logs can be used for long-lived sawtimber products, compared to more pulp resulting from clearcutting, (3) the shelterwood cut encourages growth of subcanopy trees by opening up the forest canopy to increasing light penetration. Decomposition of onsite harvest slash and of wastes created during timber processing releases CO{sub 2} to the atmosphere, thus offsetting some of the C sequestered in vegetation. Decomposition of soil C and dead roots may also be temporarily stimulated by increased light penetration and warming of the forest floor. Quantification of these processes and their net effect is needed. We began studying C sequestration in a planned shelterwood harvest at the Howland Forest in central Maine in 2000. The harvest took place in 2002 by the International Paper Corporation, who assisted us to track the fates of harvest products (Scott et al., 2004, Environmental Management 33: S9-S22). Here we present the results of intensive on-site studies of the decay of harvest slash, soil respiration, growth of the remaining trees, and net ecosystem exchange (NEE) of CO{sub 2} during the first six years following the harvest. These results are combined with calculations of C in persisting off-site harvest products to estimate the net C consequences to date of this commercial shelterwood harvest operation. Tower-based eddy covariance is an ideal method for this study, as it integrates all C fluxes in and out of the forest over a large 'footprint' area and can reveal how the net C flux, as well as gross primary productivity and respiration, change following harvest. Because the size of this experiment precludes large-scale replication, we are use a paired-airshed approach, similar to classic large-scale paired watershed experiments. Measurements of biomass and C fluxes in control and treatment stands were compared during a pre-treatment calibration period, and then divergence from pre-treatment relationships between the two sites measured after the harvest treatment. Forests store carbon (C) as they accumulate biomass. Many forests are also commercial sources of timber and wood fiber. In most C accounting budgets, forest harvesting is usually considered to cause a net release of C from the terrestrial biosphere to the atmosphere. However, it might also be possible for commercial use of forests to contribute to terrestrial sequestration of C. The objective of the our research project is to determine whether shelterwood cutting regimes now being adopted in the commercial forests of Maine and other areas of the country can achieve these multiple goals.« less

Greenhouse gas release from arctic permafrost: positive feedback to climate warming (Invited)

NASA Astrophysics Data System (ADS)

Walter Anthony, K. M.; Zimov, S. A.

2009-12-01

The release of carbon (C) in the form of greenhouse gases from thawing permafrost is one of the most likely and important positive feedbacks from the land to the atmosphere in a warmer world. Perennially frozen ground, known as permafrost, covers 20 percent of the Earth’s land surface. Recent accounting for C stored as far as 80m beneath the surface in permafrost (950 billion tons) more than doubles previous inventory estimates and is comparable to the current atmospheric CO2 burden of 750 billion tons. Permafrost organic C accumulated over tens of thousands of years. In its frozen state this C is sequestered from the atmosphere, mitigating climate warming. Long term borehole from Siberia and North America attest that permafrost is thawing. A third to half of permafrost is now within a degree to a degree and a half of thawing. In places where permafrost temperature crosses the critical 0°C threshold, ice melts causing thermokarst (ground surface collapse). Thermokarst features such as sink holes, pits, slope failure, mud flows, and the formation, expansion, and drainage of thaw lakes are widespread, up to 90% of the land area in some areas of the Arctic. Dating of features revealed that this process has been going on for the past 10,000 years, since the Earth entered the most recent interglacial warm period. However, satellite records during the past 55 years suggest that permafrost thaw in some regions is accelerating. What will happen to the climate as the rest of the permafrost thaws? When permafrost thaws, organic C is made available to microbes, which rapidly degrade it, producing greenhouse gases such as CO2 and methane (CH4, 25 times the global warming potential of CO2 over 100 years). A particularly important region for greenhouse gas emissions is the Siberian Yedoma Ice Complex (10^6 km2), a Pliestocene-aged permafrost type that contains roughly half of the Arctic’s permafrost C stock. Based on patterns of yedoma degradation during the present interglacial period, estimates of the amount of C remaining in permafrost today, long term field measurements, laboratory incubation experiments, and mass balance calculations of the efficiency of CH4 production from thawed permafrost, we predict that at least 50 billion tons of CH4 (equivalent to 10 times the current atmospheric methane burden) will escape from thermokarst lakes in Siberia as yedoma thaws. More CH4 will be released from the remainder of arctic lakes. Under current projections of warming and thaw in the Arctic (7-8 deg C by 2100), thermokarst will release 0.1-0.2 billion tons CH4 yr-1 by 2100, an order of magnitude more than its current source strength, adding another 20-40% of all human and natural sources of CH4 to the atmosphere. Frozen soils which thaw under aerobic conditions will produce CO2 with projected emissions of ~0.5-1.0 billion tons C yr-1, constituting approximately 10% of modern anthropogenic emission.

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

NASA Astrophysics Data System (ADS)

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

2017-10-01

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

Effects of atmospheric composition on respiratory behavior, weight loss, and appearance of Camembert-type cheeses during chamber ripening.

PubMed

Picque, D; Leclercq-Perlat, M-N; Corrieu, G

2006-08-01

Respiratory activity, weight loss, and appearance of Camembert-type cheeses were studied during chamber ripening in relation to atmospheric composition. Cheese ripening was carried out in chambers under continuously renewed, periodically renewed, or nonrenewed gaseous atmospheres or under a CO(2) concentration kept constant at either 2 or 6% throughout the chamber-ripening process. It was found that overall atmospheric composition, and especially CO(2) concentration, of the ripening chamber affected respiratory activity. When CO(2) was maintained at either 2 or 6%, O(2) consumption and CO(2) production (and their kinetics) were higher compared with ripening trials carried out without regulating CO(2) concentration over time. Global weight loss was maximal under continuously renewed atmospheric conditions. In this case, the airflow increased exchanges between cheeses and the atmosphere. The ratio between water evaporation and CO(2) release also depended on atmospheric composition, especially CO(2) concentration. The thickening of the creamy underrind increased more quickly when CO(2) was present in the chamber from the beginning of the ripening process. However, CO(2) concentrations higher than 2% negatively influenced the appearance of the cheeses.

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

USGS Publications Warehouse

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

2002-01-01

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

Analysis of Geologic Parameters on the Performance of CO2-Plume Geothermal (CPG) Systems in a Multi-Layered Reservoirs

NASA Astrophysics Data System (ADS)

Garapati, N.; Randolph, J.; Saar, M. O.

2013-12-01

CO2-Plume Geothermal (CPG) involves injection of CO2 as a working fluid to extract heat from naturally high permeable sedimentary basins. The injected CO2 forms a large subsurface CO2 plume that absorbs heat from the geothermal reservoir and eventually buoyantly rises to the surface. The heat density of sedimentary basins is typically relatively low.However, this drawback is likely counteracted by the large accessible volume of natural reservoirs compared to artificial, hydrofractured, and thus small-scale, reservoirs. Furthermore, supercritical CO2has a large mobility (inverse kinematic viscosity) and expansibility compared to water resulting in the formation of a strong thermosiphon which eliminates the need for parasitic pumping power requirements and significantly increasing electricity production efficiency. Simultaneously, the life span of the geothermal power plant can be increased by operating the CPG system such that it depletes the geothermal reservoir heat slowly. Because the produced CO2 is reinjected into the ground with the main CO2 sequestration stream coming from a CO2 emitter, all of the CO2 is ultimately geologically sequestered resulting in a CO2 sequestering geothermal power plant with a negative carbon footprint. Conventional geothermal process requires pumping of huge amount of water for the propagation of the fractures in the reservoir, but CPG process eliminates this requirement and conserves water resources. Here, we present results for performance of a CPG system as a function of various geologic properties of multilayered systemsincludingpermeability anisotropy, rock thermal conductivity, geothermal gradient, reservoir depth and initial native brine salinity as well as spacing between the injection and production wells. The model consists of a 50 m thick, radially symmetric grid with a semi-analytic heat exchange and no fluid flow at the top and bottom boundaries and no fluid and heat flow at the lateral boundaries. We design Plackett-Burman experiments resulting in 16 simulations for the seven parameters investigated. The reservoir is divided into 3-, 4-, or 5- layer systems with log-normal permeability distributions. We consider 10 sets of values for each case resulting in a total of 16x3x10 =480 simulations.We analyze the performance of the system to maximize the amount of heat energy extracted, minimize reservoir temperature depletion and maximize the CO2concentration in the produced fluid. Achieving the latter objective reduces power system problems as Welch and Boyle (GRC Trans. 2009) found that CO2 concentration should be >94% in the systems they investigated.

North America carbon dioxide sources and sinks: magnitude, attribution, and uncertainty

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

King, Anthony W.; Hayes, Daniel J.; Huntzinger, Deborah N.

2012-12-01

North America is both a source and sink of atmospheric CO2. Sources, predominately fossil-fuel combustion in the United States along with contributions from deforestation in Mexico, add CO2 to the atmosphere. Most North America ecosystems, particularly regrowing forests in the United States, are sinks for atmospheric CO2. CO2 is removed from the atmosphere in photosynthesis, converted into biomass and stored as carbon in vegetation, soil and wood products. Fossil-fuel emissions dominate the North American source-sink balance. North America is a net source of atmospheric CO2 with ecosystem sinks balancing approximately 35% of fossil-fuel CO2 emissions from North America.

Carbon Sequestration and Fertility after Centennial Time Scale Incorporation of Charcoal into Soil

PubMed Central

Criscuoli, Irene; Alberti, Giorgio; Baronti, Silvia; Favilli, Filippo; Martinez, Cristina; Calzolari, Costanza; Pusceddu, Emanuela; Rumpel, Cornelia; Viola, Roberto; Miglietta, Franco

2014-01-01

The addition of pyrogenic carbon (C) in the soil is considered a potential strategy to achieve direct C sequestration and potential reduction of non-CO2 greenhouse gas emissions. In this paper, we investigated the long term effects of charcoal addition on C sequestration and soil physico-chemical properties by studying a series of abandoned charcoal hearths in the Eastern Alps of Italy established in the XIX century. This natural setting can be seen as an analogue of a deliberate experiment with replications. Carbon sequestration was assessed indirectly by comparing the amount of pyrogenic C present in the hearths (23.3±4.7 kg C m−2) with the estimated amount of charcoal that was left on the soil after the carbonization (29.3±5.1 kg C m−2). After taking into account uncertainty associated with parameters’ estimation, we were able to conclude that 80±21% of the C originally added to the soil via charcoal can still be found there and that charcoal has an overall Mean Residence Time of 650±139 years, thus supporting the view that charcoal incorporation is an effective way to sequester atmospheric CO2. We also observed an overall change in the physical properties (hydrophobicity and bulk density) of charcoal hearth soils and an accumulation of nutrients compared to the adjacent soil without charcoal. We caution, however, that our site-specific results should not be generalized without further study. PMID:24614647

Formation and loss of humic substances during decomposition in a pine forest floor

USGS Publications Warehouse

Qualls, R.G.; Takiyama, A.; Wershaw, R. L.

2003-01-01

Since twice as much C is sequestered in soils as is contained in the atmosphere, the factors controlling the decomposition rate of soil C are important to the assessment of the effects of climatic change. The formation of chemically resistant humic substances might be an important process controlling recycling of CO2 to the atmosphere. Our objectives were to measure the rate of formation and loss of humic substances during 13 yr of litter decomposition. We placed nets on the floor of a white pine (Pinus strobus) forest to separate each annual layer of litter for 13 yr and measured humic substance concentration using NaOH extraction followed by chromatographic fractionation. The humic acid fraction increased from 2.1% of the C in litterfall to 15.7% after 1 yr. On a grams per square meter (g m-2) basis the humic substance fraction increased during the first year and then declined, with a half decay time (t1/2) of 5.1 yr, which was significantly slower than the bulk litter (t1/2 = 3.9 yr). The carboxylic C concentration estimated from 13C nuclear magnetic resonance (NMR) increased in the litter over time, though total mass of carboxylic acid C in the forest floor also declined over the 13-yr period (t1/2 = 4.6 yr). While humic substances in the forest floor decomposed at a somewhat slower rate than bulk litter during Years 1 to 13, they decomposed much faster than has been calculated from 14C dating of the refractory fraction of organic matter in the mineral soil.

Coupled nutrient cycling determines tropical forest trajectory under elevated CO2.

NASA Astrophysics Data System (ADS)

Bouskill, N.; Zhu, Q.; Riley, W. J.

2017-12-01

Tropical forests have a disproportionate capacity to affect Earth's climate relative to their areal extent. Despite covering just 12 % of land surface, tropical forests account for 35 % of global net primary productivity and are among the most significant of terrestrial carbon stores. As atmospheric CO2 concentrations increase over the next century, the capacity of tropical forests to assimilate and sequester anthropogenic CO2 depends on limitation by multiple factors, including the availability of soil nutrients. Phosphorus availability has been considered to be the primary factor limiting metabolic processes within tropical forests. However, recent evidence points towards strong spatial and temporal co-limitation of tropical forests by both nitrogen and phosphorus. Here, we use the Accelerated Climate Modeling for Energy (ACME) Land Model (ALMv1-ECA-CNP) to examine how nutrient cycles interact and affect the trajectory of the tropical forest carbon sink under, (i) external nutrient input, (ii) climate (iii) elevated CO2, and (iv) a combination of 1-3. ALMv1 includes recent theoretical advances in representing belowground competition between roots, microbes and minerals for N and P uptake, explicit interactions between the nitrogen and phosphorus cycles (e.g., phosphatase production and nitrogen fixation), the dynamic internal allocation of plant N and P resources, and the integration of global datasets of plant physiological traits. We report nutrient fertilization (N, P, N+P) predictions for four sites in the tropics (El Verde, Puerto Rico, Barro Colorado Island, Panama, Manaus, Brazil and the Osa Peninsula, Coast Rica) to short-term nutrient fertilization (N, P, N+P), and benchmarking of the model against a meta-analysis of forest fertilization experiments. Subsequent simulations focus on the interaction of the carbon, nitrogen, and phosphorus cycles across the tropics with a focus on the implications of coupled nutrient cycling and the fate of the tropical forest carbon sink. Our results highlight the importance of transient CNP allocation, leaf-level stoichiometric controls on photosynthesis, and trade-offs between above and belowground plant investments.

Gross primary production of a semiarid grassland is enhanced by six years of exposure to elevated atmospheric CO2, warming, and irrigation.

NASA Astrophysics Data System (ADS)

Ryan, E.; Ogle, K.; Peltier, D.; Williams, D. G.; Pendall, E.

2014-12-01

The goal of this study was to quantify interannual variation of gross primary production (GPP) and evaluate potential drivers of GPP with global change using the Prairie Heating and CO2 Enrichment (PHACE) experiment in semiarid grassland in southeastern Wyoming. PHACE consists of the treatments: control, warming only, elevated CO2 (eCO2) only, eCO2 and warming, and irrigation only. We expected that GPP would be most strongly influenced by interannual variability in precipitation under all PHACE treatments, soil water availability under eCO2, and nitrogen availability. GPP data were obtained from paired measurements of net ecosystem exchange (NEE) and ecosystem respiration (Reco; GPP = Reco - NEE) made on 2-4 week intervals over six growing seasons (2007-2012). Soil temperature (T), soil water content (SWC), vapor pressure deficit (VPD), and photosynthetically active radiation (PAR) were continuously recorded at the plot (T, SWC) and site (VPD, PAR) scales. Annual, plot-level aboveground plant nitrogen content (N) was measured during peak biomass. We fit a non-linear light-response model to the GPP data within a Bayesian framework, and modeled the maximum GPP rate (Gmax) and canopy light-use efficiency (Q) as functions of N and current and antecedent SWC, T, and VPD. The model fit the GPP data well (R2 = 0.64), and regardless of the PHACE treatment the most important drivers of GPP were N (for Gmax), VPD (Gmax and Q), antecedent T (Gmax), and antecedent VPD (Q). Model simulations predicted that annual GPP increased on average by about 16% with eCO2, 14% with warming, 12% with eCO2 and warming, and 23% with irrigation. For four of the six years, annual GPP was significantly affected by either eCO2 alone or when combined with warming. The increase in annual GPP under irrigation was similar to the increase under eCO2 during a dry year (2012), but irrigation stimulated GPP to a greater degree than eCO2 during wet years (2008, 2009). Hence, increases in GPP under eCO2 appear to be indirectly due to increases in SWC, especially under dry conditions. These results suggest that future climate scenarios will lead to more productive grasslands in semiarid regions, but the overall response of the C cycle and the potential for these systems to sequester greater C will depend on the magnitude and direction of both the Reco and GPP responses.

Quantifying fossil fuel CO2 from continuous measurements of APO: a novel approach

NASA Astrophysics Data System (ADS)

Pickers, Penelope; Manning, Andrew C.; Forster, Grant L.; van der Laan, Sander; Wilson, Phil A.; Wenger, Angelina; Meijer, Harro A. J.; Oram, David E.; Sturges, William T.

2016-04-01

Using atmospheric measurements to accurately quantify CO2 emissions from fossil fuel sources requires the separation of biospheric and anthropogenic CO2 fluxes. The ability to quantify the fossil fuel component of CO2 (ffCO2) from atmospheric measurements enables more accurate 'top-down' verification of CO2 emissions inventories, which frequently have large uncertainty. Typically, ffCO2 is quantified (in ppm units) from discrete atmospheric measurements of Δ14CO2, combined with higher resolution atmospheric CO measurements, and with knowledge of CO:ffCO2 ratios. In the United Kingdom (UK), however, measurements of Δ14CO2 are often significantly biased by nuclear power plant influences, which limit the use of this approach. We present a novel approach for quantifying ffCO2 using measurements of APO (Atmospheric Potential Oxygen; a tracer derived from concurrent measurements of CO2 and O2) from two measurement sites in Norfolk, UK. Our approach is similar to that used for quantifying ffCO2 from CO measurements (ffCO2(CO)), whereby ffCO2(APO) = (APOmeas - APObg)/RAPO, where (APOmeas - APObg) is the APO deviation from the background, and RAPO is the APO:CO2 combustion ratio for fossil fuel. Time varying values of RAPO are calculated from the global gridded COFFEE (CO2 release and Oxygen uptake from Fossil Fuel Emission Estimate) dataset, combined with NAME (Numerical Atmospheric-dispersion Modelling Environment) transport model footprints. We compare our ffCO2(APO) results to results obtained using the ffCO2(CO) method, using CO:CO2 fossil fuel emission ratios (RCO) from the EDGAR (Emission Database for Global Atmospheric Research) database. We find that the APO ffCO2 quantification method is more precise than the CO method, owing primarily to a smaller range of possible APO:CO2 fossil fuel emission ratios, compared to the CO:CO2 emission ratio range. Using a long-term dataset of atmospheric O2, CO2, CO and Δ14CO2 from Lutjewad, The Netherlands, we examine the accuracy of our ffCO2(APO) method, and assess the potential of using APO to quantify ffCO2 independently from Δ14CO2 measurements, which, as well as being unreliable in many UK regions, are very costly. Using APO to quantify ffCO2 has significant policy relevance, with the potential to provide more accurate and more precise top-down verification of fossil fuel emissions.

Microbiological and biochemical aspects of Camembert-type cheeses depend on atmospheric composition in the ripening chamber.

PubMed

Leclercq-Perlat, M-N; Picque, D; Riahi, H; Corrieu, G

2006-08-01

Camembert-type cheeses were prepared from pasteurized milk seeded with Kluyveromyces lactis, Geotrichum candidum, Penicillium camemberti, and Brevibacterium aurantiacum. Microorganism growth and biochemical dynamics were studied in relation to ripening chamber CO(2) atmospheric composition using 31 descriptors based on kinetic data. The chamber ripening was carried out under 5 different controlled atmospheres: continuously renewed atmosphere, periodically renewed atmosphere, no renewed atmosphere, and 2 for which CO(2) was either 2% or 6%. All microorganism dynamics depended on CO(2) level. Kluyveromyces lactis was not sensitive to CO(2) during its growth phases, but its death did depend on it. An increase of CO(2) led to a significant improvement in G. candidum. Penicillium camemberti mycelium development was enhanced by 2% CO(2). The equilibrium between P. camemberti and G. candidum populations was disrupted in favor of the yeast when CO(2) was higher than 4%. Growth of B. aurantiacum depended more on O(2) than on CO(2). Two ripening progressions were observed in relation to the presence of CO(2) at the beginning of ripening: in the presence of CO(2), the ripening was fast-slow, and in the absence of CO(2), it was slow-fast. The underrind was too runny if CO(2) was equal to or higher than 6%. The nitrogen substrate progressions were slightly related to ripening chamber CO(2) and O(2) levels. During chamber ripening, the best atmospheric condition to produce an optimum between microorganism growth, biochemical dynamics, and cheese appearance was a constant CO(2) level close to 2%.

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

PubMed

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

2018-01-01

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

Observational constraints on the global atmospheric CO2 budget

NASA Technical Reports Server (NTRS)

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

1990-01-01

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

Bolide impacts and the oxidation state of carbon in the Earth's early atmosphere

NASA Technical Reports Server (NTRS)

Kasting, J. F.

1992-01-01

A one-dimensional photochemical model was used to examine the effect of bolide impacts on the oxidation state of Earth's primitive atmosphere. The impact rate should have been high prior to 3.8 Ga before present, based on evidence derived from the Moon. Impacts of comets or carbonaceous asteroids should have enhanced the atmospheric CO/CO2 ratio by bringing in CO ice and/or organic carbon that can be oxidized to CO in the impact plume. Ordinary chondritic impactors would contain elemental iron that could have reacted with ambient CO2 to give CO. Nitric oxide (NO) should also have been produced by reaction between ambient CO2 and N2 in the hot impact plumes. High NO concentrations increase the atmospheric CO/CO2 ratio by increasing the rainout rate of oxidized gases. According to the model, atmospheric CO/CO2 ratios of unity or greater are possible during the first several hundred million years of Earth's history, provided that dissolved CO was not rapidly oxidized to bicarbonate in the ocean. Specifically, high atmospheric CO/CO2 ratios are possible if either: (1) the climate was cool (like today's climate), so that hydration of dissolved CO to formate was slow, or (2) the formate formed from CO was efficiently converted into volatile, reduced carbon compounds, such as methane. A high atmospheric CO/CO2 ratio may have helped to facilitate prebiotic synthesis by enhancing the production rates of hydrogen cyanide and formaldehyde. Formaldehyde may have been produced even more efficiently by photochemical reduction of bicarbonate and formate in Fe(++)-rich surface waters.

Maximum leaf conductance driven by CO2 effects on stomatal size and density over geologic time.

PubMed

Franks, Peter J; Beerling, David J

2009-06-23

Stomatal pores are microscopic structures on the epidermis of leaves formed by 2 specialized guard cells that control the exchange of water vapor and CO(2) between plants and the atmosphere. Stomatal size (S) and density (D) determine maximum leaf diffusive (stomatal) conductance of CO(2) (g(c(max))) to sites of assimilation. Although large variations in D observed in the fossil record have been correlated with atmospheric CO(2), the crucial significance of similarly large variations in S has been overlooked. Here, we use physical diffusion theory to explain why large changes in S necessarily accompanied the changes in D and atmospheric CO(2) over the last 400 million years. In particular, we show that high densities of small stomata are the only way to attain the highest g(cmax) values required to counter CO(2)"starvation" at low atmospheric CO(2) concentrations. This explains cycles of increasing D and decreasing S evident in the fossil history of stomata under the CO(2) impoverished atmospheres of the Permo-Carboniferous and Cenozoic glaciations. The pattern was reversed under rising atmospheric CO(2) regimes. Selection for small S was crucial for attaining high g(cmax) under falling atmospheric CO(2) and, therefore, may represent a mechanism linking CO(2) and the increasing gas-exchange capacity of land plants over geologic time.

Maximum leaf conductance driven by CO2 effects on stomatal size and density over geologic time

PubMed Central

Franks, Peter J.; Beerling, David J.

2009-01-01

Stomatal pores are microscopic structures on the epidermis of leaves formed by 2 specialized guard cells that control the exchange of water vapor and CO2 between plants and the atmosphere. Stomatal size (S) and density (D) determine maximum leaf diffusive (stomatal) conductance of CO2 (gcmax) to sites of assimilation. Although large variations in D observed in the fossil record have been correlated with atmospheric CO2, the crucial significance of similarly large variations in S has been overlooked. Here, we use physical diffusion theory to explain why large changes in S necessarily accompanied the changes in D and atmospheric CO2 over the last 400 million years. In particular, we show that high densities of small stomata are the only way to attain the highest gcmax values required to counter CO2“starvation” at low atmospheric CO2 concentrations. This explains cycles of increasing D and decreasing S evident in the fossil history of stomata under the CO2 impoverished atmospheres of the Permo-Carboniferous and Cenozoic glaciations. The pattern was reversed under rising atmospheric CO2 regimes. Selection for small S was crucial for attaining high gcmax under falling atmospheric CO2 and, therefore, may represent a mechanism linking CO2 and the increasing gas-exchange capacity of land plants over geologic time. PMID:19506250

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

NASA Technical Reports Server (NTRS)

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

1985-01-01

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

Modeling hormonal control of cambium proliferation.

PubMed

Oles, Vladyslav; Panchenko, Alexander; Smertenko, Andrei

2017-01-01

Rise of atmospheric CO2 is one of the main causes of global warming. Catastrophic climate change can be avoided by reducing emissions and increasing sequestration of CO2. Trees are known to sequester CO2 during photosynthesis, and then store it as wood biomass. Thus, breeding of trees with higher wood yield would mitigate global warming as well as augment production of renewable construction materials, energy, and industrial feedstock. Wood is made of cellulose-rich xylem cells produced through proliferation of a specialized stem cell niche called cambium. Importance of cambium in xylem cells production makes it an ideal target for the tree breeding programs; however our knowledge about control of cambium proliferation remains limited. The morphology and regulation of cambium are different from those of stem cell niches that control axial growth. For this reason, translating the knowledge about axial growth to radial growth has limited use. Furthermore, genetic approaches cannot be easily applied because overlaying tissues conceal cambium from direct observation and complicate identification of mutants. To overcome the paucity of experimental tools in cambium biology, we constructed a Boolean network CARENET (CAmbium REgulation gene NETwork) for modelling cambium activity, which includes the key transcription factors WOX4 and HD-ZIP III as well as their potential regulators. Our simulations predict that: (1) auxin, cytokinin, gibberellin, and brassinosteroids act cooperatively in promoting transcription of WOX4 and HD-ZIP III; (2) auxin and cytokinin pathways negatively regulate each other; (3) hormonal pathways act redundantly in sustaining cambium activity; (4) individual cambium cells can have diverse molecular identities. CARENET can be extended to include components of other signalling pathways and be integrated with models of xylem and phloem differentiation. Such extended models would facilitate breeding trees with higher wood yield.

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

NASA Astrophysics Data System (ADS)

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

2017-03-01

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

Lidar Measurements of Atmospheric CO2 From Regional to Global Scales

NASA Technical Reports Server (NTRS)

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

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

PubMed

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

2011-01-01

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

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

NASA Astrophysics Data System (ADS)

Zickfeld, K.; Azevedo, D.

2017-12-01

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

Practical method of CO.sub.2 sequestration

DOEpatents

Goswami, D Yogi [Gainesville, FL; Lee, Man Su [Houston, TX; Kothurkar, Nikhil K [Tampa, FL; Stefanakos, Elias K [Tampa, FL

2011-03-01

A process and device to capture of CO.sub.2 at its originating source, such as a power plant, is disclosed. Absorbent material is recharged by desorbing CO.sub.2, so that it may be sequestered or used in another application. Continual recharging results in loss of absorbent surface area, due to pore plugging and sintering of particles. Calcium oxide or calcium hydroxide was immobilized to a fibrous ceramic-based fabric substrate as a thin film and sintered, creating an absorbent material. The samples were characterized, showing continuous cyclic carbonation conversions between about 62% and 75% under mild calcination conditions at 750.degree. C. and no CO.sub.2 in N.sub.2. Under the more severe calcination condition at 850.degree. C. and 20 wt % CO.sub.2 in N.sub.2, yttria fabric was superior to alumina as a substrate for carbon dioxide capture and the reactivity of the calcium oxide absorbent immobilized to yttria was maintained at the same level in the 12 cycles.

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

DOE Data Explorer

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

1998-01-01

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

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

PubMed

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

2016-10-27

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

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

NASA Astrophysics Data System (ADS)

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

2016-12-01

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

Methodology for calculation of carbon balances for biofuel crops production

NASA Astrophysics Data System (ADS)

Gerlfand, I.; Hamilton, S. K.; Snapp, S. S.; Robertson, G. P.

2012-04-01

Understanding the carbon balance implications for different biofuel crop production systems is important for the development of decision making tools and policies. We present here a detailed methodology for assessing carbon balances in agricultural and natural ecosystems. We use 20 years of data from Long-term Ecological Research (LTER) experiments at the Kellogg Biological Station (KBS), combined with models to produce farm level CO2 balances for different management practices. We compared four grain and one forage systems in the U.S. Midwest: corn (Zea mays) - soybean (Glycine max) - wheat (Triticum aestivum) rotations managed with (1) conventional tillage, (2) no till, (3) low chemical input, and (4) biologically-based (organic) practices; and (5) continuous alfalfa (Medicago sativa). In addition we use an abandoned agricultural field (successionnal ecosystem) as reference system. Measurements include fluxes of N2O and CH4, soil organic carbon change, agricultural yields, and agricultural inputs (e.g. fertilization and farm fuel use). In addition to measurements, we model carbon offsets associated with the use of bioenergy from agriculturally produced crops. Our analysis shows the importance of establishing appropriate system boundaries for carbon balance calculations. We explore how different assumptions regarding production methods and emission factors affect overall conclusions on carbon balances of different agricultural systems. Our results show management practices that have major the most important effects on carbon balances. Overall, agricultural management with conventional tillage was found to be a net CO2 source to the atmosphere, while agricultural management under reduced tillage, low input, or organic management sequestered carbon at rates of 93, -23, -51, and -14 g CO2e m-2 yr-1, respectively for conventionally tilled, no-till, low-input, and organically managed ecosystems. Perennial systems (alfalfa and the successionnal fields) showed net carbon sequestration of -44 and -382 g CO2e m-2 yr-1, respectively. When studied systems were assumed to be used for bioenergy production, all system exhibited carbon sequestration -- between -149 and -841 g CO2e m-2 yr-1, for conventionally tilled and successionnal ecosystems, respectively.

Potential for negative emissions of greenhouse gases (CO2, CH4 and N2O) through coastal peatland re-establishment: Novel insights from high frequency flux data at meter and kilometer scales

NASA Astrophysics Data System (ADS)

Windham-Myers, Lisamarie; Bergamaschi, Brian; Anderson, Frank; Knox, Sara; Miller, Robin; Fujii, Roger

2018-04-01

High productivity temperate wetlands that accrete peat via belowground biomass (peatlands) may be managed for climate mitigation benefits due to their global distribution and notably negative emissions of atmospheric carbon dioxide (CO2) through rapid storage of carbon (C) in anoxic soils. Net emissions of additional greenhouse gases (GHG)—methane (CH4) and nitrous oxide (N2O)—are more difficult to predict and monitor due to fine-scale temporal and spatial variability, but can potentially reverse the climate mitigation benefits resulting from CO2 uptake. To support management decisions and modeling, we collected continuous 96 hour high frequency GHG flux data for CO2, CH4 and N2O at multiple scales—static chambers (1 Hz) and eddy covariance (10 Hz)—during peak productivity in a well-studied, impounded coastal peatland in California’s Sacramento Delta with high annual rates of C fluxes, sequestering 2065 ± 150 g CO2 m‑2 y‑1 and emitting 64.5 ± 2.4 g CH4 m‑2 y‑1. Chambers (n = 6) showed strong spatial variability along a hydrologic gradient from inlet to interior plots. Daily (24 hour) net CO2 uptake (NEE) was highest near inlet locations and fell dramatically along the flowpath (‑25 to ‑3.8 to +2.64 g CO2 m‑2 d‑1). In contrast, daily net CH4 flux increased along the flowpath (0.39 to 0.62 to 0.88 g CH4 m‑2 d‑1), such that sites of high daily CO2 uptake were sites of low CH4 emission. Distributed, continuous chamber data exposed five novel insights, and at least two important datagaps for wetland GHG management, including: (1) increasing dominance of CH4 ebullition fluxes (15%–32% of total) along the flowpath and (2) net negative N2O flux across all sites as measured during a 4 day period of peak biomass (‑1.7 mg N2O m‑2 d‑1 0.51 g CO2 eq m‑2 d‑1). The net negative emissions of re-established peat-accreting wetlands are notably high, but may be poorly estimated by models that do not consider within-wetland spatial variability due to water flowpaths.

Mapping the Mineral Resource Base for Mineral Carbon-Dioxide Sequestration in the Conterminous United States

USGS Publications Warehouse

Krevor, S.C.; Graves, C.R.; Van Gosen, B. S.; McCafferty, A.E.

2009-01-01

This database provides information on the occurrence of ultramafic rocks in the conterminous United States that are suitable for sequestering captured carbon dioxide in mineral form, also known as mineral carbon-dioxide sequestration. Mineral carbon-dioxide sequestration is a proposed greenhouse gas mitigation technology whereby carbon dioxide (CO2) is disposed of by reacting it with calcium or magnesium silicate minerals to form a solid magnesium or calcium carbonate product. The technology offers a large capacity to permanently store CO2 in an environmentally benign form via a process that takes little effort to verify or monitor after disposal. These characteristics are unique among its peers in greenhouse gas disposal technologies. The 2005 Intergovernmental Panel on Climate Change report on Carbon Dioxide Capture and Storage suggested that a major gap in mineral CO2 sequestration is locating the magnesium-silicate bedrock available to sequester the carbon dioxide. It is generally known that silicate minerals with high concentrations of magnesium are suitable for mineral carbonation. However, no assessment has been made in the United States that details their geographical distribution and extent, nor has anyone evaluated their potential for use in mineral carbonation. Researchers at Columbia University and the U.S. Geological Survey have developed a digital geologic database of ultramafic rocks in the conterminous United States. Data were compiled from varied-scale geologic maps of magnesium-silicate ultramafic rocks. The focus of our national-scale map is entirely on ultramafic rock types, which typically consist primarily of olivine- and serpentine-rich rocks. These rock types are potentially suitable as source material for mineral CO2 sequestration.

Carbonate-H2O2 Leaching for Sequestering Uranium from Seawater

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

Pan, Horng-Bin; Weisheng, Liao; Wai, Chien

Uranium adsorbed on amidoxime-based polyethylene fiber in simulated seawater can be quantitatively eluted at room temperature using 1M Na2CO3 containing 0.1 M H2O2. This efficient elution process is probably due to formation of an extremely stable uranyl-peroxo-carbonato complex in the carbonate solution. After washing with water, the sorbent can be reused with little loss of uranium loading capacity. Possible existence of this stable uranyl species in ocean water is also discussed.

Chemistry of Earth's Putative Steam Atmosphere

NASA Astrophysics Data System (ADS)

Fegley, B.; Schaefer, L.

2007-12-01

The concept of a steam atmosphere generated by impact devolatilization of planetesimals accreted during Earth's formation is over 20 years old (Matsui and Abe, 1986; Lange and Ahrens, 1982). Surprisingly, with the possible exception of a few qualitative remarks, no one has critically assessed this scenario. We use thermochemical equilibrium and, where relevant, thermochemical kinetic calculations to model the chemistry of the "steam" atmosphere produced by impact volatilization of different types of accreting material. We present results for our nominal conditions (1500 K, total P = 100 bar). We also studied the effects of variable temperature and total pressure. The composition of the accreting material is modeled using average compositions of the Orgueil CI chondrite, the Murchison CM2 chondrite, the Allende CV3 chondrite, average ordinary (H, L, LL) chondrites, and average enstatite (EH, EL) chondrites. The major gases released from CI and CM chondritic material are H2O, CO2, H2, H2S, CO, CH4, and SO2 in decreasing order of abundance. About 10% of the atmosphere is CO2. The major gases released from CV chondritic material are CO2, H2O, CO, H2, and SO2 in decreasing order of abundance. About 20% of the total atmosphere is steam. The major gases released from average ordinary chondritic material are H2, CO, H2O, CO2, CH4, H2S, and N2 in decreasing order of abundance. The "steam" atmosphere is predominantly H2 + CO with steam being about 10% of the total atmosphere. The major gases released from EH chondritic material are H2, CO, H2O, CO2, N2, and CH4 in decreasing order of abundance. The "steam" atmosphere is predominantly H2 + CO with about 10% of the total atmosphere as steam. This work was supported by the NASA Astrobiology and Origins Programs.

Effect of high-oxygen and high-carbon-dioxide atmospheres on strawberry flavor and other quality traits.

PubMed

Pérez, A G; Sanz, C

2001-05-01

The effect of high-oxygen atmospheres on strawberry flavor was studied. Strawberry fruits (Fragariax ananassa Duch. cv. Camarosa) were stored at 8 degrees C in four different atmospheres: air, 5% O(2)/20% CO(2), 80% O(2)/20% CO(2), and 90% O(2)/10% CO(2). Changes in several quality parameters were evaluated. Atmospheres combining high O(2) and high CO(2) were the most effective in preventing fungal growth and enhancing strawberry firmness. Other quality parameters such as color, titrable acidity, sugars and organic acids distribution, off-flavor development, and aroma were only mildly affected by superatmospheric O(2) levels. After one week of storage, unexpected high contents of off-flavor related compounds were found in the 80% O(2)/20% CO(2) and 90% O(2)/10% CO(2) atmospheres. Evidence of an altered ester biosynthesis was also found in fruits stored under these high-O(2) atmospheres. Data obtained suggest that stress induced by high CO(2) and stress induced by high O(2) have an additive effect on strawberry flavor alteration.

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

NASA Technical Reports Server (NTRS)

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

2000-01-01

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

[Direct Observation on the Temporal and Spatial Patterns of the CO2 Concentration in the Atmospheric of Nanjing Urban Canyon in Summer].

PubMed

Gao, Yun-qiu; Liu, Shou-dong; Hu, Ning; Wang, Shu-min; Deng, Li-chen; Yu, Zhou; Zhang, Zhen; Li, Xu-hui

2015-07-01

Direct observation of urban atmospheric CO2 concentration is vital for the research in the contribution of anthropogenic activity to the atmospheric abundance since cities are important CO2 sources. The observations of the atmospheric CO2 concentration at multiple sites/heights can help us learn more about the temporal and spatial patterns and influencing mechanisms. In this study, the CO2 concentration was observed at 5 sites (east, west, south, north and middle) in the main city area of Nanjing from July 18 to 25, 2014, and the vertical profile of atmospheric CO2 concentration was measured in the middle site at 3 heights (30 m, 65 m and 110 m). The results indicated that: (1) An obvious vertical CO2 gradient was found, with higher CO2 concentration [molar fraction of 427. 3 x 10(-6) (±18. 2 x 10(-6))] in the lower layer due to the strong influences of anthropogenic emissions, and lower CO2 concentration in the upper layers [411. 8 x 10(-6) (±15. 0 x 10(-6)) and 410. 9 x 10(-6) (±14. 6 x 10(-6)) at 65 and 110 m respectively] for the well-mixed condition. The CO2 concentration was higher and the vertical gradient was larger when the atmosphere was stable. (2) The spatial distribution pattern of CO2 concentration was dominated by wind and atmospheric stability. During the observation, the CO2 concentration in the southwest was higher than that in the northeast region with the CO2 concentration difference of 7. 8 x 10(-6), because the northwest wind was prevalent. And the CO2 concentration difference reduced with increasing wind speed since stronger wind diluted CO2 more efficiently. The more stable the atmosphere was, the higher the CO2 concentration was. (3) An obvious diurnal variation of CO2 concentration was shown in the 5 sites. A peak value occurred during the morning rush hours, the valley value occurred around 17:00 (Local time) and another high value occurred around 19:00 because of evening rush hour sometimes.

Deep ocean nutrients imply large latitudinal variation in particle transfer efficiency.

PubMed

Weber, Thomas; Cram, Jacob A; Leung, Shirley W; DeVries, Timothy; Deutsch, Curtis

2016-08-02

The "transfer efficiency" of sinking organic particles through the mesopelagic zone and into the deep ocean is a critical determinant of the atmosphere-ocean partition of carbon dioxide (CO2). Our ability to detect large-scale spatial variations in transfer efficiency is limited by the scarcity and uncertainties of particle flux data. Here we reconstruct deep ocean particle fluxes by diagnosing the rate of nutrient accumulation along transport pathways in a data-constrained ocean circulation model. Combined with estimates of organic matter export from the surface, these diagnosed fluxes reveal a global pattern of transfer efficiency to 1,000 m that is high (∼25%) at high latitudes and low (∼5%) in subtropical gyres, with intermediate values in the tropics. This pattern is well correlated with spatial variations in phytoplankton community structure and the export of ballast minerals, which control the size and density of sinking particles. These findings accentuate the importance of high-latitude oceans in sequestering carbon over long timescales, and highlight potential impacts on remineralization depth as phytoplankton communities respond to a warming climate.

Deep ocean nutrients imply large latitudinal variation in particle transfer efficiency

NASA Astrophysics Data System (ADS)

Weber, Thomas; Cram, Jacob A.; Leung, Shirley W.; DeVries, Timothy; Deutsch, Curtis

2016-08-01

The “transfer efficiency” of sinking organic particles through the mesopelagic zone and into the deep ocean is a critical determinant of the atmosphere-ocean partition of carbon dioxide (CO2). Our ability to detect large-scale spatial variations in transfer efficiency is limited by the scarcity and uncertainties of particle flux data. Here we reconstruct deep ocean particle fluxes by diagnosing the rate of nutrient accumulation along transport pathways in a data-constrained ocean circulation model. Combined with estimates of organic matter export from the surface, these diagnosed fluxes reveal a global pattern of transfer efficiency to 1,000 m that is high (˜25%) at high latitudes and low (˜5%) in subtropical gyres, with intermediate values in the tropics. This pattern is well correlated with spatial variations in phytoplankton community structure and the export of ballast minerals, which control the size and density of sinking particles. These findings accentuate the importance of high-latitude oceans in sequestering carbon over long timescales, and highlight potential impacts on remineralization depth as phytoplankton communities respond to a warming climate.

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

PubMed Central

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

2016-01-01

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

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

DOE PAGES

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

2016-11-08

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

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

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

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

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

Simulated effect of calcification feedback on atmospheric CO2 and ocean acidification

PubMed Central

Zhang, Han; Cao, Long

2016-01-01

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

Physical disintegration of biochar: An overlooked process

EPA Science Inventory

Biochar is a form of black carbon (BC) that has been documented to be resistant to both microbial and chemical degradation pathways as well as simultaneously sequestering atmospheric carbon (C) and postulated to act as a soil fertility agent by providing critical inorganic plant ...

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

PubMed

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

2012-04-01

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

Protecting terrestrial ecosystems and the climate through a global carbon market.

PubMed

Bonnie, Robert; Carey, Melissa; Petsonk, Annie

2002-08-15

Protecting terrestrial ecosystems through international environmental laws requires the development of economic mechanisms that value the Earth's natural systems. The major international treaties to address ecosystem protection lack meaningful binding obligations and the requisite financial instruments to affect large-scale conservation. The Kyoto Protocol's emissions-trading framework creates economic incentives for nations to reduce greenhouse-gas (GHG) emissions cost effectively. Incorporating GHG impacts from land-use activities into this system would create a market for an important ecosystem service provided by forests and agricultural lands: sequestration of atmospheric carbon. This would spur conservation efforts while reducing the 20% of anthropogenic CO(2) emissions produced by land-use change, particularly tropical deforestation. The Kyoto negotiations surrounding land-use activities have been hampered by a lack of robust carbon inventory data. Moreover, the Protocol's provisions agreed to in Kyoto made it difficult to incorporate carbon-sequestering land-use activities into the emissions-trading framework without undermining the atmospheric GHG reductions contemplated in the treaty. Subsequent negotiations since 1997 failed to produce a crediting system that provides meaningful incentives for enhanced carbon sequestration. Notably, credit for reducing rates of tropical deforestation was explicitly excluded from the Protocol. Ultimately, an effective GHG emissions-trading framework will require full carbon accounting for all emissions and sequestration from terrestrial ecosystems. Improved inventory systems and capacity building for developing nations will, therefore, be necessary.

Accelerated weathering of limestone for CO2 mitigation opportunities for the stone and cement industries

USGS Publications Warehouse

Langer, W.H.; Juan, C.A.S.; Rau, G.H.; Caldeira, K.

2009-01-01

Large amounts of limestone fines coproduced during the processing of crushed limestone may be useful in the sequestration of carbon dioxide (CO 2). Accelerated weathering of limestone (AWL) is proposed as a low-tech method to capture and sequester CO2 from fossil fuel-fired power plants and other point-sources such as cement manufacturing. AWL reactants are readily available, inexpensive, and environmentally benign. Waste CO 2 is hydrated with water to produce carbonic acid, which then reacts with and is neutralized by limestone fines, thus converting CO2 gas to dissolved calcium bicarbonate. AWL waste products can be disposed of in the ocean. Feasibility requires access to an inexpensive source of limestone and to seawater, thus limiting AWL facilities within about 10 km of the coastline. The majority of U.S. coastal power generating facilities are within economical transport distance of limestone resources. AWL presents opportunities for collaborative efforts among the crushed stone industry, electrical utilities, cement manufactures, and research scientists.

Sustainable biochar to mitigate global climate change

PubMed Central

Woolf, Dominic; Amonette, James E.; Street-Perrott, F. Alayne; Lehmann, Johannes; Joseph, Stephen

2010-01-01

Production of biochar (the carbon (C)-rich solid formed by pyrolysis of biomass) and its storage in soils have been suggested as a means of abating climate change by sequestering carbon, while simultaneously providing energy and increasing crop yields. Substantial uncertainties exist, however, regarding the impact, capacity and sustainability of biochar at the global level. In this paper we estimate the maximum sustainable technical potential of biochar to mitigate climate change. Annual net emissions of carbon dioxide (CO2), methane and nitrous oxide could be reduced by a maximum of 1.8 Pg CO2-C equivalent (CO2-Ce) per year (12% of current anthropogenic CO2-Ce emissions; 1 Pg=1 Gt), and total net emissions over the course of a century by 130 Pg CO2-Ce, without endangering food security, habitat or soil conservation. Biochar has a larger climate-change mitigation potential than combustion of the same sustainably procured biomass for bioenergy, except when fertile soils are amended while coal is the fuel being offset. PMID:20975722

Evaluating Soil Carbon Sequestration in Central Iowa

NASA Astrophysics Data System (ADS)

Doraiswamy, P. C.; Hunt, E. R.; McCarty, G. W.; Daughtry, C. S.; Izaurralde, C.

2005-12-01

The potential for reducing atmospheric carbon dioxide (CO2) concentration through landuse and management of agricultural systems is of great interest worldwide. Agricultural soils can be a source of CO2 when not properly managed but can also be a sink for sequestering CO2 through proper soil and crop management. The EPIC-CENTURY biogeochemical model was used to simulate the baseline level of soil carbon from soil survey data and project changes in soil organic carbon (SOC) under different tillage and crop management practices for corn and soybean crops. The study was conducted in central Iowa (50 km x 100 km) to simulate changes in soil carbon over the next 50 years. The simulations were conducted in two phases; initially a 25-year period (1971-1995) was simulated using conventional tillage practices since there was a transition in new management after 1995. In the second 25-year period (1996-2020), four different modeling scenarios were applied namely; conventional tillage, mulch tillage, no-tillage and no-tillage with a rye cover crop over the winter. The model simulation results showed potential gains in soil carbon in the top layers of the soil for conservation tillage. The simulations were made at a spatial resolution of 1.6 km x 1.6 km and mapped for the study area. There was a mean reduction in soil organic carbon of 0.095 T/ha per year over the 25-year period starting with 1996 for the conventional tillage practice. However, for management practices of mulch tillage, no tillage and no tillage with cover crop there was an increase in soil organic carbon of 0.12, 0.202 and 0.263 T/ha respectively over the same 25-year period. These results are in general similar to studies conducted in this region.

An Integrated, Low Temperature Process to Capture and Sequester Carbon Dioxide from Industrial Emissions

NASA Astrophysics Data System (ADS)

Wendlandt, R. F.; Foremski, J. J.

2013-12-01

Laboratory experiments show that it is possible to integrate (1) the chemistry of serpentine dissolution, (2) capture of CO2 gas from the combustion of natural gas and coal-fired power plants using aqueous amine-based solvents, (3) long-term CO2 sequestration via solid phase carbonate precipitation, and (4) capture solvent regeneration with acid recycling in a single, continuous process. In our process, magnesium is released from serpentine at 300°C via heat treatment with ammonium sulfate salts or at temperatures as low as 50°C via reaction with sulfuric acid. We have also demonstrated that various solid carbonate phases can be precipitated directly from aqueous amine-based (NH3, MEA, DMEA) CO2 capture solvent solutions at room temperature. Direct precipitation from the capture solvent enables regenerating CO2 capture solvent without the need for heat and without the need to compress the CO2 off gas. We propose that known low-temperature electrochemical methods can be integrated with this process to regenerate the aqueous amine capture solvent and recycle acid for dissolution of magnesium-bearing mineral feedstocks and magnesium release. Although the direct precipitation of magnesite at ambient conditions remains elusive, experimental results demonstrate that at temperatures ranging from 20°C to 60°C, either nesquehonite Mg(HCO3)(OH)●2H2O or a double salt with the formula [NH4]2Mg(CO3)2●4H2O or an amorphous magnesium carbonate precipitate directly from the capture solvent. These phases are less desirable for CO2 sequestration than magnesite because they potentially remove constituents (water, ammonia) from the reaction system, reducing the overall efficiency of the sequestration process. Accordingly, the integrated process can be accomplished with minimal energy consumption and loss of CO2 capture and acid solvents, and a net generation of 1 to 4 moles of H2O/6 moles of CO2 sequestered (depending on the solid carbonate precipitate and amount of produced H2 and O2 gas reacted to produce heat and water). Features of the integrated process include the following: 1) the four separate processes have compatible chemistry, enabling design of an integrated, continuous process scheme for CO2 capture and sequestration; 2) all 4 stages of the process can be conducted at ambient or slightly elevated temperatures; 3) precipitating carbonate directly from the capture solvent eliminates the need for costly CO2 gas compression; and 4) recycling the acid used for serpentine dissolution and the solvent used for CO2 capture reduces feed stock costs.

Sequestration Options for the West Coast States

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

Myer, Larry

The West Coast Regional Carbon Sequestration Partnership (WESTCARB) is one of seven partnerships that have been established by the U.S. Department of Energy (DOE) to evaluate carbon capture and sequestration (CCS) technologies best suited for different regions of the country. The West Coast Region comprises Arizona, California, Nevada, Oregon, Washington, Alaska, and British Columbia. Led by the California Energy Commission, WESTCARB is a consortium of about 70 organizations, including state natural resource and environmental protection agencies; national laboratories and universities; private companies working on carbon dioxide (CO{sub 2}) capture, transportation, and storage technologies; utilities; oil and gas companies; nonprofit organizations; and policy/governance coordinating organizations. Both terrestrial and geologic sequestration options were evaluated in the Region during the 18-month Phase I project. A centralized Geographic Information System (GIS) database of stationary source, geologic and terrestrial sink data was developed. The GIS layer of source locations was attributed with CO{sub 2} emissions and other data and a spreadsheet was developed to estimate capture costs for the sources in the region. Phase I characterization of regional geological sinks shows that geologic storage opportunities exist in the WESTCARB region in each of the major technology areas: saline formations, oil and gas reservoirs, and coal beds. California offers outstanding sequestration opportunities because of its large capacity and the potential of value-added benefits from enhanced oil recovery (EOR) and enhanced gas recovery. The estimate for storage capacity of saline formations in the ten largest basins in California ranges from about 150 to about 500 Gt of CO{sub 2}, the potential CO{sub 2}-EOR storage was estimated to be 3.4 Gt, and the cumulative production from gas reservoirs suggests a CO{sub 2} storage capacity of 1.7 Gt. A GIS-based method for source-sink matching was implemented and preliminary marginal cost curves developed, which showed that 20, 40, or 80 Mega tonnes (Mt) of CO{sub 2} per year could be sequestered in California at a cost ofmore » $31/tonne (t), $35/t, or $$50/t, respectively. Phase I also addressed key issues affecting deployment of CCS technologies, including storage-site monitoring, injection regulations, and health and environmental risks. A framework for screening and ranking candidate sites for geologic CO{sub 2} storage on the basis of HSE risk was developed. A webbased, state-by-state compilation of current regulations for injection wells, and permits/contracts for land use changes, was developed, and modeling studies were carried out to assess the application of a number of different geophysical techniques for monitoring geologic sequestration. Public outreach activities resulted in heightened awareness of sequestration among state, community and industry leaders in the Region. Assessment of the changes in carbon stocks in agricultural lands showed that Washington, Oregon and Arizona were CO{sub 2} sources for the period from 1987 to 1997. Over the same period, forest carbon stocks decreased in Washington, but increased in Oregon and Arizona. Results of the terrestrial supply curve analyses showed that afforestation of rangelands and crop lands offer major sequestration opportunities; at a price of $$20 per t CO{sub 2}, more than 1,233 MMT could be sequestered over 40-years in Washington and more than 1,813 MMT could be sequestered in Oregon.« less

Bolide impacts and the oxidation state of carbon in the earth's early atmosphere

NASA Technical Reports Server (NTRS)

Kasting, James F.

1990-01-01

A one-dimensional photochemical model was used to examine the effect of bolide impacts on the oxidation state of earth's primitive atmosphere. The impact rate should have been high prior to 3.8 Ga before present, based on evidence derived from the moon. Impacts of comets or carbonaceous asteroids should have enhanced the atmospheric CO/CO2 ratio by bringing in CO ice and/or organic carbon that can be oxidized to CO in the impact plume. Ordinary chondritic impactors would contain elemental iron that could have reacted with ambient CO2 to give CO. Nitric oxide (NO) should also have been produced by reaction between ambient CO2 and N2 in the hot impact plumes. High NO concentrations increase the atmospheric CO/CO2 ratio by increasing the rainout rate of oxidized gases. According to the model, atmospheric CO/CO2 ratios of unity or greater are possible during the first several hundred million years of earth's history, provided that dissolved CO was not rapidly oxidized to bicarbonate in the ocean.

Partially Interpenetrated NbO Topology Metal–Organic Framework Exhibiting Selective Gas Adsorption

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

Verma, Gaurav; Kumar, Sanjay; Pham, Tony

2017-03-29

We report on the first partially interpenetrated metal–organic framework (MOF) with NbO topology for its ability to separate methane from carbon dioxide and permanently sequester the greenhouse gas CO2. The MOF, Cu2(pbpta) (H4pbpta = 4,4',4'',4'''-(1,4-phenylenbis(pyridine-4,2-6-triyl))-tetrabenzoic acid), crystallizes in the monoclinic C2/m space group and has a 2537 m2/g Brunauer, Emmett and Teller surface area with an 1.06 cm3/g pore volume. The MOF exhibits selective adsorption of CO2 over CH4 as well as that of C2H6 and C2H4 over CH4. Cu2(pbpta) additionally shows excellent catalytic efficacy for the cycloaddition reaction of CO2 with epoxides to produce industrially important cyclic carbonates usingmore » solvent-free conditions.« less

The Global Carbon Cycle: It's a Small World

NASA Astrophysics Data System (ADS)

Ineson, Philip; Milcu, Alexander; Subke, Jens-Arne; Wildman, Dennis; Anderson, Robert; Manning, Peter; Heinemeyer, Andreas

2010-05-01

Predicting future atmospheric concentrations of carbon dioxide (CO2), together with the impacts of these changes on global climate, are some of the most urgent and important challenges facing mankind. Modelling is the only way in which such predictions can be made, leading to the current generation of increasingly complex computer simulations, with associated concerns about embedded assumptions and conflicting model outputs. Alongside analysis of past climates, the GCMs currently represent our only hope of establishing the importance of potential runaway positive feedbacks linking climate change and atmospheric greenhouse gases yet the incorporation of necessary biospheric responses into GCMs markedly increases the uncertainty of predictions. Analysis of the importance of the major components of the global carbon (C) cycle reveals that an understanding of the conditions under which the terrestrial biosphere could switch from an overall carbon (C) sink to a source is critical to our ability to make future climate predictions. Here we present an alternative approach to assessing the short term biotic (plant and soil) sensitivities to elevated temperature and atmospheric CO2 through the use of a purely physical analogue. Centred on the concept of materially-closed systems containing scaled-down ratios of the global C stocks for the atmosphere, vegetation and soil we show that, in these model systems, the terrestrial biosphere is able to buffer a rise of 3oC even when coupled to very strong CO2-temperature positive feedbacks. The system respiratory response appears to be extremely well linked to temperature and is critical in deciding atmospheric concentrations of CO2. Simulated anthropogenic emissions of CO2 into the model systems showed an initial corresponding increase in atmospheric CO2 but, somewhat surprisingly, CO2 concentrations levelled off at ca. 480 p.p.m.v., despite continuing additions of CO2. Experiments were performed in which reversion of atmospheric temperatures, or cessation of CO2 additions, showed rapid and proportionate decreases in atmospheric CO2 concentrations. The results indicate that short term terrestrial feedbacks are not sufficient to induce a CO2-temperature runaway scenario and suggest that predictions of atmospheric CO2 by current GCMs may under-estimate the CO2 fertilisation effect on plants and, hence, over-estimate future atmospheric CO2 increases. Perhaps, more importantly, the experiments show that the impacts of imposed elevated CO2 and temperature increase can be reversed. Whilst clearly representing a simplified version of terrestrial CO2 dynamics, it is proposed that closed system research represents a new form of test-bed for validation of processes represented within digital global CO2 models.

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

PubMed

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

2013-03-01

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

Eddy covariance measurements of greenhouse gases from a restored and rewetted raised bog ecosystem.

NASA Astrophysics Data System (ADS)

Lee, S. C.; Christen, A.; Black, T. A.; Johnson, M. S.; Ketler, R.; Nesic, Z.; Merkens, M.

2015-12-01

Wetland ecosystems play a significant role in the global carbon (C) cycle. Wetlands act as a major long-term storage of carbon by sequestrating carbon-dioxide (CO2) from the atmosphere. Meanwhile, they can emit significant amounts of methane (CH4) due to anaerobic microbial decomposition. The Burns Bog Ecological Conservancy Area (BBECA) is recognized as one of Canada's largest undeveloped natural areas retained within an urban area. Historically, it has been substantially reduced in size and degraded by peat mining and agriculture. Since 2005, the bog has been declared a conservancy area, and the restoration efforts in BBECA focus on rewetting the disturbed ecosystems to promote a transition back to a raised bog. A pilot study measured CH4, CO2 and N2O exchanges in 2014 and concluded to monitor CO2, CH4 fluxes continuously. From the perspective of greenhouse gas (GHG) emissions, CO2 sequestered in bog needs to be protected and additional CO2 and CH4 emissions due to land-cover change need to be reduced by wise management. In this study, we measured the growing-season (June-September) fluxes of CO2 and CH4 exchange using eddy covariance (EC). A floating platform with an EC system for both CO2 (closed-path) and CH4 (open-path) began operation in June 2015. During the growing-season, gross ecosystem photosynthesis (GEP) and ecosystem respiration (Re) averaged 5.87 g C m-2 day-1 and 2.02 g C m-2 day-1, respectively. The magnitude of GEP and Re were lower than in previous studies of pristine northern peatlands. The daily average CH4 emission was 0.99 (±1.14) g C m-2 day-1 and it was higher than in most previous studies. We also characterized how environmental factors affected the seasonal dynamics of these exchanges in this disturbed peatland. Our measurements showed that soil temperature and soil water content were major drivers of seasonal changes of GHG fluxes. The daily average GHG warming potential (GWP) of the emissions in the growing seasons (from CO2 and CH4) totals to 37.09 g CO2e m-2 day-1. CH4 was the significant constributor (99 % of GHG emissions) indicating that GHG exchange due to photosynthesis and respiration was of secondary order. Although oxygen limitation due to the high water table caused by the restoration strategy suppressed the Re it also promoted substantial CH4 formation under anoxic conditions.

Understanding Climate Policy Data Needs. NASA Carbon Monitoring System Briefing: Characterizing Flux Uncertainty, Washington D.C., 11 January 2012

NASA Technical Reports Server (NTRS)

Brown, Molly E.; Macauley, Molly

2012-01-01

Climate policy in the United States is currently guided by public-private partnerships and actions at the local and state levels. This mitigation strategy is made up of programs that focus on energy efficiency, renewable energy, agricultural practices and implementation of technologies to reduce greenhouse gases. How will policy makers know if these strategies are working, particularly at the scales at which they are being implemented? The NASA Carbon Monitoring System (CMS) will provide information on carbon dioxide fluxes derived from observations of earth's land, ocean and atmosphere used in state of the art models describing their interactions. This new modeling system could be used to assess the impact of specific policy interventions on CO2 reductions, enabling an iterative, results-oriented policy process. In January of 2012, the CMS team held a meeting with carbon policy and decision makers in Washington DC to describe the developing modeling system to policy makers. The NASA CMS will develop pilot studies to provide information across a range of spatial scales, consider carbon storage in biomass, and improve measures of the atmospheric distribution of carbon dioxide. The pilot involves multiple institutions (four NASA centers as well as several universities) and over 20 scientists in its work. This pilot study will generate CO2 flux maps for two years using observational constraints in NASA's state-of -the-art models. Bottom-up surface flux estimates will be computed using data-constrained land and ocean models; comparison of the different techniques will provide some knowledge of uncertainty in these estimates. Ensembles of atmospheric carbon distributions will be computed using an atmospheric general circulation model (GEOS-5), with perturbations to the surface fluxes and to transport. Top-down flux estimates will be computed from observed atmospheric CO2 distributions (ACOS/GOSAT retrievals) alongside the forward-model fields, in conjunction with an inverse approach based on the CO2 model of GEOS ]Chem. The forward model ensembles will be used to build understanding of relationships among surface flux perturbations, transport uncertainty and atmospheric carbon concentration. This will help construct uncertainty estimates and information on the true spatial resolution of the top-down flux calculations. The relationship between the top-down and bottom-up flux distributions will be documented. Because the goal of NASA CMS is to be policy relevant, the scientists involved in the flux modeling pilot need to understand and be focused on the needs of the climate policy and decision making community. If policy makers are to use CMS products, they must be aware of the modeling effort and begin to design policies that can be evaluated with information. Improving estimates of carbon sequestered in forests, for example, will require information on the spatial variability of forest biomass that is far more explicit than is presently possible using only ground observations. Carbon mitigation policies being implemented by cities around the United States could be designed with the CMS data in mind, enabling sequential evaluation and subsequent improvements in incentives, structures and programs. The success of climate mitigation programs being implemented in the United States today will hang on the depth of the relationship between scientists and their policy and decision making counterparts. Ensuring that there is two-way communication between data providers and users is important for the success both of the policies and the scientific products meant to support them..

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

PubMed

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

2015-10-16

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

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

Treesearch

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

2012-01-01

The southeastern landscape is composed of agricultural and forest systems that can store carbon (C) in standing biomass and soil. Research is needed to quantify the effects of elevated atmospheric carbon dioxide (CO2) on terrestrial C dynamics including CO2 release back to the atmosphere and soil sequestration. Longleaf...

Impact of atmospheric CO2 levels on continental silicate weathering

NASA Astrophysics Data System (ADS)

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

2010-07-01

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

Developing a Comprehensive Risk Assessment Framework for Geological Storage CO 2

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

Duncan, Ian

2014-08-31

The operational risks for CCS projects include: risks of capturing, compressing, transporting and injecting CO₂; risks of well blowouts; risk that CO 2 will leak into shallow aquifers and contaminate potable water; and risk that sequestered CO 2 will leak into the atmosphere. This report examines these risks by using information on the risks associated with analogue activities such as CO 2 based enhanced oil recovery (CO 2-EOR), natural gas storage and acid gas disposal. We have developed a new analysis of pipeline risk based on Bayesian statistical analysis. Bayesian theory probabilities may describe states of partial knowledge, even perhapsmore » those related to non-repeatable events. The Bayesian approach enables both utilizing existing data and at the same time having the capability to adsorb new information thus to lower uncertainty in our understanding of complex systems. Incident rates for both natural gas and CO 2 pipelines have been widely used in papers and reports on risk of CO 2 pipelines as proxies for the individual risk created by such pipelines. Published risk studies of CO 2 pipelines suggest that the individual risk associated with CO2 pipelines is between 10 -3 and 10 -4, which reflects risk levels approaching those of mountain climbing, which many would find unacceptably high. This report concludes, based on a careful analysis of natural gas pipeline failures, suggests that the individual risk of CO 2 pipelines is likely in the range of 10-6 to 10-7, a risk range considered in the acceptable to negligible range in most countries. If, as is commonly thought, pipelines represent the highest risk component of CCS outside of the capture plant, then this conclusion suggests that most (if not all) previous quantitative- risk assessments of components of CCS may be orders of magnitude to high. The potential lethality of unexpected CO 2 releases from pipelines or wells are arguably the highest risk aspects of CO 2 enhanced oil recovery (CO2-EOR), carbon capture, and storage (CCS). Assertions in the CCS literature, that CO 2 levels of 10% for ten minutes, or 20 to 30% for a few minutes are lethal to humans, are not supported by the available evidence. The results of published experiments with animals exposed to CO 2, from mice to monkeys, at both normal and depleted oxygen levels, suggest that lethal levels of CO 2 toxicity are in the range 50 to 60%. These experiments demonstrate that CO 2 does not kill by asphyxia, but rather is toxic at high concentrations. It is concluded that quantitative risk assessments of CCS have overestimated the risk of fatalities by using values of lethality a factor two to six lower than the values estimated in this paper. In many dispersion models of CO 2 releases from pipelines, no fatalities would be predicted if appropriate levels of lethality for CO 2 had been used in the analysis.« less

Sustainable biochar to mitigate global climate change

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

Woolf, Dominic; Amonette, James E.; Street-Perrott, F. A.

2010-08-10

Production of biochar (the carbon-rich solid formed by pyrolysis of biomass), in combination with its storage in soils, has been suggested as a means to abate anthropogenic climate change, while simultaneously increasing crop yields. The climate mitigation potential stems primarily from the highly recalcitrant nature of biochar, which slows the rate at which photosynthetically fixed carbon is returned to the atmosphere. Significant uncertainties exist, however, regarding the impact, capacity, and sustainability of biochar for carbon capture and storage when scaled to the global level. Previous estimates, based on simple assumptions, vary widely. Here we show that, subject to strict environmentalmore » and modest economic constraints on biomass procurement and biochar production methods, annual net emissions of CO2, CH4 and N2O could be reduced by 1.1 - 1.9 Pg CO2-C equivalent (CO2-Ce)/yr (7 - 13% of current anthropogenic CO2-Ce emissions; 1Pg = 1 Gt). Over one century, cumulative net emissions of these gases could be reduced by 72-140 Pg CO2-Ce. The lower end of this range uses currently untapped residues and wastes; the upper end requires substantial alteration to global biomass management, but would not endanger food security, habitat or soil conservation. Half the avoided emissions are due to the net C sequestered as biochar, one-quarter to replacement of fossil-fuel energy by pyrolysis energy, and one-quarter to avoided emissions of CH4 and N2O. The total mitigation potential is 18-30% greater than if the same biomass were combusted to produce energy. Despite limited data for the decomposition rate of biochar in soils and the effects of biochar additions on soil greenhouse-gas fluxes, sensitivity within realistic ranges of these parameters is small, resulting in an uncertainty of ±8% (±1 s.d.) in our estimates. Achieving these mitigation results requires, however, that biochar production be performed using only low-emissions technologies and feedstocks obtained sustainably, with minimal carbon debt incurred from land-use change.« less

Enhanced CO2 sequestration by a novel microalga: Scenedesmus obliquus SA1 isolated from bio-diversity hotspot region of Assam, India.

PubMed

Basu, Samarpita; Roy, Abhijit Sarma; Mohanty, Kaustubha; Ghoshal, Aloke K

2013-09-01

The present study aimed to isolate a high CO2 and temperature tolerant microalga capable of sequestering CO2 from flue gas. Microalga strain SA1 was isolated from a freshwater body of Assam and identified as Scenedesmus obliquus (KC733762). At 13.8±1.5% CO2 and 25 °C, maximum biomass (4.975±0.003 g L(-1)) and maximum CO2 fixation rate (252.883±0.361 mg L(-1) d(-1)) were obtained which were higher than most of the relevant studies. At elevated temperature (40 °C) and 13.8±1.5% CO2 maximum biomass (0.883±0.001 g L(-1)) was obtained. The carbohydrate, protein, lipid, and chlorophyll content of the CO2 treated SA1 were 30.87±0.64%, 9.48±1.65%, 33.04±0.46% and 6.03±0.19% respectively, which were higher than previous reports. Thus, SA1 could prove to be a potential candidate for CO2 sequestration from flue gas as well as for the production of value added substances. Copyright © 2013 Elsevier Ltd. All rights reserved.

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

NASA Technical Reports Server (NTRS)

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

1990-01-01

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

Atmospheric CO2 Variability Observed From ASCENDS Flight Campaigns

NASA Technical Reports Server (NTRS)

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

Effects of Syn-Pandemic Reforestation on Atmospheric Carbon Dioxide From 1500 to 1700 A.D.

NASA Astrophysics Data System (ADS)

Nevle, R. J.; Bird, D. K.

2005-12-01

Recent analysis of paleoclimate proxies suggests that biomass burning by humans during the past eight millennia produced quantities of CO2 sufficient to counteract the effects of decreasing insolation driven by orbital variations and thus prevented ice sheet expansion. Correlation between periods of declining population and biomass burning, such as implied by the synchroneity of the American pandemics and decreasing atmospheric CO2 concentration during the 16th-18th centuries, provides an important test of the extent to which pre-industrial anthropogenic activity affected the atmospheric greenhouse gas budget. Numerous studies have attributed the ~5 ppm decline of atmospheric CO2 concentration, as well as the synchronous ~0.1 per mil increase of the δ13C of atmospheric CO2 between 1500 and 1700 A.D., to the effects of Little Ice Age cooling. However, this interpretation is not supported by recent multiproxy-based surface temperature reconstructions, which demonstrate a diminutive global temperature anomaly of ~0.1 C that was unlikely to have independently produced the distinct effect observed in atmospheric CO2 concentration. Alternatively, it is possible that a decline in CO2 concentration driven by massive reforestation produced cooling as a by-product. The timing and magnitude of changes in both the concentration and carbon-isotope composition of atmospheric CO2 recorded by globally distributed climate proxies from the tropics (sponges), temperate latitudes (tree rings), and polar regions (ice cores) are compatible with fixation of >10 Gt C due to reforestation. Reforestation, which explains pre-industrial atmospheric CO2 variations between 1500 and 1700 A.D. in a manner more consistent with the global surface temperature record than explanations requiring substantial cooling, presumably occurred on lands that were cultivated and seasonally burned, then subsequently abandoned, by indigenous Americans who perished in pandemics during European conquest. The present proxy data point to reforestation in the wake of the American pandemic, with its consequent affects on atmospheric CO2, as unique in human history. These findings redefine the duration and extent of human activities affecting composition of the atmosphere during the past millennium. The anthropogenic influence on the partial pressure of atmospheric CO2 since ~1800 A.D. is well documented by the exponential rise in concentration and simultaneous decline in δ13C of atmospheric CO2, but these recent trends represent dramatic reversals in the behavior of atmospheric CO2 concentration and δ13C prior to the Industrial Revolution between 1500 and 1700. During this time the concentration of atmospheric CO2 decreased and its δ13C increased due to land use changes resulting from pandemics that killed ~90% of the indigenous American population (~50 million people).

C/O Ratio as a Dimension for Characterizing Exoplanetary Atmospheres

NASA Astrophysics Data System (ADS)

Madhusudhan, Nikku

2012-10-01

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

C/O RATIO AS A DIMENSION FOR CHARACTERIZING EXOPLANETARY ATMOSPHERES

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

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

2012-10-10

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

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

NASA Astrophysics Data System (ADS)

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

2015-12-01

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

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

NASA Astrophysics Data System (ADS)

Oschlies, A.

2009-08-01

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

Carbonate-H₂O₂ leaching for sequestering uranium from seawater.

PubMed

Pan, Horng-Bin; Liao, Weisheng; Wai, Chien M; Oyola, Yatsandra; Janke, Christopher J; Tian, Guoxin; Rao, Linfeng

2014-07-28

Uranium adsorbed on amidoxime-based polyethylene fiber in simulated seawater can be quantitatively eluted at room temperature using 1 M Na2CO3 containing 0.1 M H2O2. This efficient elution process is probably due to the formation of an extremely stable uranyl-peroxo-carbonato complex in the carbonate solution. After washing with water, the sorbent can be reused with minimal loss of uranium loading capacity. Possible existence of this stable uranyl species in ocean water is also discussed.

Venus: The case for a wet origin and a runaway greenhouse

NASA Technical Reports Server (NTRS)

Kasting, J. F.

1992-01-01

To one interested in atmospheric evolution, the most intriguing aspect of our neighboring planet Venus is its lack of water. Measurements made by Pioneer Venus and by Several Venera spacecraft indicate that the present water abundance in Venus' lower atmosphere is of the order of 20 to 200 ppmv, or 3 x 10( exp -6) to 3 x 10 (exp -5) of the amount of water in Earth's oceans. The exact depletion factor is uncertain, in part because of an unexplained vertical gradient in H2O concentration in the lowest 10 km of the venusian atmosphere, but the general scarcity of water is well established. The interesting question, then, is: Was venus deficient in water when it formed and, if not, where did its water go? The conclusion that Venus was originally wet is consistent with its large endowment of other volatiles and with the enhanced D/H ratio in the present atmosphere. The most likely mechanism by which Venus could have lost its water is by the development of a runaway or moist greenhouse atmosphere followed by photodissociation of water vapor and escape of hydrogen to space. Climate model calculations that neglect cloud albedo feedback predict the existence of two critical transitions in atmospheric behavior at high solar fluxes: (1) at a solar flux of approximately 1.1 times the value at Earth's orbit, S(o), the abundance of stratospheric water vapor increases dramatically, permitting rapid escape of hydrogen to space (termed a moist greenhouse) and (2) at a solar flux of approximately 1.4 S(o), the oceans vaporize entirely, creating a true runaway greenhouse. If cloudiness increases at high surface temperatures, as seems likely, and if the dominant effect of clouds is to cool the planet by reflecting incident solar radiation, the actual solar flux required to create moist or runaway conditions would be higher than the values quoted above. Early in solar system history, solar luminosity was about 25 percent to 30 percent less than today, putting the flux at Venus' orbit in the range of 1.34 S(o) to 1.43 S(o). Thus, it is possible that Venus had liquid water on its surface for several hundred million years following its formation. Paradoxically, this might have facilitated water loss by sequestering atmospheric CO2 in carbonate rocks and by providing an effective medium for surface oxidation.

Seaweeds and halophytes to remove carbon from the atmosphere

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

Glenn, E.P.; Kent, K.J.; Thompson, T.L.

1991-02-01

The utility industry and other interested parties have investigated strategies to mitigate the buildup of atmospheric CO{sub 2}. One option that has been considered is the planting of trees on a massive scale to absorb carbon through photosynthesis. A dilemma of using tree plantations, however, is that they might occupy land that will be needed for food production or other needs for an expected doubling of human population in the tropical regions. We evaluated seaweeds and salt-tolerant terrestrial plants (halophytes) to be grown on the coastal shelves and salt deserts of the world as possible alternatives to tree plantations. Anmore » estimated 1.3 {times} 10{sup 6} km{sup 2} of continental shelf and 1.3 {times} 10{sup 6} km{sup 2} of salt desert may be usable for seaweed and halophyte plantations. The production rates of managed seaweed and halophyte plantings are similar to managed tree plantations. Seaweeds and halophytes could conceivably absorb 10--20% of annual fossil fuel carbon emissions through biomass production, similar to estimates made for tree plantations. Present costs of halophyte biomass production are similar to costs of tree biomass production, whereas seaweed biomass is much more expensive to produce using existing technologies. Storage of seaweed carbon might be accomplished by allowing it to enter the sediment detritus chain whereas halophyte carbon might be sequestered in the soil, or used as biomass fuel. As has been concluded for reforestation, these saline biomass crops could at best help delay rather than solve the carbon dioxide build-up problem. 1 fig., 13 tabs.« less

Apportionment of carbon dioxide over central Europe: insights from combined measurements of atmospheric CO2 mixing ratios and carbon isotope composition

NASA Astrophysics Data System (ADS)

Zimnoch, M.; Jelen, D.; Galkowski, M.; Kuc, T.; Necki, J.; Chmura, L.; Gorczyca, Z.; Jasek, A.; Rozanski, K.

2012-04-01

The European continent, due to high population density and numerous sources of anthropogenic CO2 emissions, plays an important role in the global carbon budget. Nowadays, precise measurements of CO2 mixing ratios performed by both global and regional monitoring networks, combined with appropriate models of carbon cycle, allow quantification of the European input to the global atmospheric CO2 load. However, measurements of CO2 mixing ratios alone cannot provide the information necessary for the apportionment of fossil-fuel related and biogenic contributions to the total CO2 burden of the regional atmosphere. Additional information is required, for instance obtained through measurements of radiocarbon content in atmospheric carbon dioxide. Radiocarbon is a particularly useful tracer for detecting fossil carbon in the atmosphere on different spatial and temporal scales. Regular observations of atmospheric CO2mixing ratios and their isotope compositions have been performed during the period of 2005-2009 at two sites located in central Europe (southern Poland). The sites, only ca. 100 km apart, represent two extreme environments with respect to the extent of anthropogenic pressure: (i) the city of Krakow, representing typical urban environment with numerous sources of anthropogenic CO2, and (ii) remote mountain site Kasprowy Wierch, relatively free of local influences. Regular, quasi-continuous measurements of CO2 mixing ratios have been performed at both sites. In addition, cumulative samples of atmospheric CO2 have been collected (weekly sampling regime for Krakow and monthly for Kasprowy Wierch) to obtain mean carbon isotope signature (14C/12C and 13C/12C ratios) of atmospheric CO2 at both sampling locations. Partitioning of the local atmospheric CO2 load at both locations has been performed using isotope- and mass balance approach. In Krakow, the average fossil-fuel related contribution to the local atmospheric CO2 load was equal to approximately 3.4%. The biogenic component turned out to be of the same magnitude. Both components revealed a distinct seasonality, with the fossil-fuel related component reaching maximum values during winter months and the biogenic component shifted in phase by ca. 6 months. Seasonality of fossil-fuel related CO2 load in the local atmosphere is linked with seasonality of local CO2sources, mostly burning of fossil fuels for heating purposes. Positive values of biogenic component indicate prevalence of the local respiration and biomass burning processes over local photosynthesis. Summer maxima of biogenic CO2 component represent mostly local respiration activity. Direct measurements of soil CO2 fluxes in the Krakow region showed an approximately 10-fold increase of those fluxes during the summer months. Partitioning of the local CO2 budget for Kasprowy Wierch site revealed large differences in the derived components when compared to urban atmosphere of Krakow: the fossil-fuel related component was ca. 5 times lower whereas the biogenic component was negative in summer, pointing to the importance of photosynthetic sink associated with extensive forests in the neighborhood of the station. The isotope- and mass balance approach was also used to derive mean monthly 13C isotope signature of fossil-fuel related CO2 emissions in Krakow. Although the derived δ13CO2 values revealed large variability, they are confined in the range of 13C isotope composition being reported for various sources of CO2 emissions in the city (burning of coal and oil, burning of methane gas, traffic).

Method for sequestering CO.sub.2 and SO.sub.2 utilizing a plurality of waste streams

DOEpatents

Soong, Yee [Monroeville, PA; Allen, Douglas E [Salem, MA; Zhu, Chen [Monroe County, IN

2011-04-12

A neutralization/sequestration process is provided for concomitantly addressing capture and sequestration of both CO.sub.2 and SO.sub.2 from industrial gas byproduct streams. The invented process concomitantly treats and minimizes bauxite residues from aluminum production processes and brine wastewater from oil/gas production processes. The benefits of this integrated approach to coincidental treatment of multiple industrial waste byproduct streams include neutralization of caustic byproduct such as bauxite residue, thereby decreasing the risk associated with the long-term storage and potential environmental of storing caustic materials, decreasing or obviating the need for costly treatment of byproduct brines, thereby eliminating the need to purchase CaO or similar scrubber reagents typically required for SO.sub.2 treatment of such gasses, and directly using CO.sub.2 from flue gas to neutralize bauxite residue/brine mixtures, without the need for costly separation of CO.sub.2 from the industrial byproduct gas stream by processes such as liquid amine-based scrubbers.

Comparison of carbon balance in Mediterranean pilot constructed wetlands vegetated with different C4 plant species.

PubMed

Barbera, Antonio C; Borin, Maurizio; Cirelli, Giuseppe L; Toscano, Attilio; Maucieri, Carmelo

2015-02-01

This study investigates carbon dioxide (CO2) and methane (CH4) emissions and carbon (C) budgets in a horizontal subsurface flow pilot-plant constructed wetland (CW) with beds vegetated with Cyperus papyrus L., Chrysopogon zizanioides (L.) Roberty, and Mischantus × giganteus Greef et Deu in the Mediterranean basin (Sicily) during the 1st year of plant growing season. At the end of the vegetative season, M. giganteus showed the higher biomass accumulation (7.4 kg m(-2)) followed by C. zizanioides (5.3 kg m(-2)) and C. papyrus (1.8 kg m(-2)). Significantly higher emissions of CO2 were detected in the summer, while CH4 emissions were maximum during spring. Cumulative CO2 emissions by C. papyrus and C. zizanioides during the monitoring period showed similar trends with final values of about 775 and 1,074 g m(-2), respectively, whereas M. giganteus emitted 3,395 g m(-2). Cumulative CH4 bed emission showed different trends for the three C4 plant species in which total gas release during the study period was for C. papyrus 12.0 g m(-2) and ten times higher for M. giganteus, while C. zizanioides bed showed the greatest CH4 cumulative emission with 240.3 g m(-2). The wastewater organic carbon abatement determined different C flux in the atmosphere. Gas fluxes were influenced both by plant species and monitored months with an average C-emitted-to-C-removed ratio for C. zizanioides, C. papyrus, and M. giganteus of 0.3, 0.5, and 0.9, respectively. The growing season C balances were positive for all vegetated beds with the highest C sequestered in the bed with M. giganteus (4.26 kg m(-2)) followed by C. zizanioides (3.78 kg m(-2)) and C. papyrus (1.89 kg m(-2)). To our knowledge, this is the first paper that presents preliminary results on CO2 and CH4 emissions from CWs vegetated with C4 plant species in Mediterranean basin during vegetative growth.

Fighting global warming by greenhouse gas removal: destroying atmospheric nitrous oxide thanks to synergies between two breakthrough technologies.

PubMed

Ming, Tingzhen; de Richter, Renaud; Shen, Sheng; Caillol, Sylvain

2016-04-01

Even if humans stop discharging CO2 into the atmosphere, the average global temperature will still increase during this century. A lot of research has been devoted to prevent and reduce the amount of carbon dioxide (CO2) emissions in the atmosphere, in order to mitigate the effects of climate change. Carbon capture and sequestration (CCS) is one of the technologies that might help to limit emissions. In complement, direct CO2 removal from the atmosphere has been proposed after the emissions have occurred. But, the removal of all the excess anthropogenic atmospheric CO2 will not be enough, due to the fact that CO2 outgases from the ocean as its solubility is dependent of its atmospheric partial pressure. Bringing back the Earth average surface temperature to pre-industrial levels would require the removal of all previously emitted CO2. Thus, the atmospheric removal of other greenhouse gases is necessary. This article proposes a combination of disrupting techniques to transform nitrous oxide (N2O), the third most important greenhouse gas (GHG) in terms of current radiative forcing, which is harmful for the ozone layer and possesses quite high global warming potential. Although several scientific publications cite "greenhouse gas removal," to our knowledge, it is the first time innovative solutions are proposed to effectively remove N2O or other GHGs from the atmosphere other than CO2.

Rocks Here Sequester Some of Mars Early Atmosphere

NASA Image and Video Library

2015-09-02

This view combines information from two instruments on NASA's Mars Reconnaissance Orbiter to map color-coded composition over the shape of the ground in a small portion of the Nili Fossae plains region of Mars' northern hemisphere. This site is part of the largest known carbonate-rich deposit on Mars. In the color coding used for this map, green indicates a carbonate-rich composition, brown indicates olivine-rich sands, and purple indicates basaltic composition. Carbon dioxide from the atmosphere on early Mars reacted with surface rocks to form carbonate, thinning the atmosphere by sequestering the carbon in the rocks. An analysis of the amount of carbon contained in Nili Fossae plains estimated the total at no more than twice the amount of carbon in the modern atmosphere of Mars, which is mostly carbon dioxide. That is much more than in all other known carbonate on Mars, but far short of enough to explain how Mars could have had a thick enough atmosphere to keep surface water from freezing during a period when rivers were cutting extensive valley networks on the Red Planet. Other possible explanations for the change from an era with rivers to dry modern Mars are being investigated. This image covers an area approximately 1.4 miles (2.3 kilometers) wide. A scale bar indicates 500 meters (1,640 feet). The full extent of the carbonate-containing deposit in the region is at least as large as Delaware and perhaps as large as Arizona. The color coding is from data acquired by the Compact Reconnaissance Imaging Spectrometer for Mars (CRISM), in observation FRT0000C968 made on Sept. 19, 2008. The base map showing land shapes is from the High Resolution Imaging Science Experiment (HiRISE) camera. It is one product from HiRISE observation ESP_010351_2020, made July 20, 2013. http://photojournal.jpl.nasa.gov/catalog/PIA19817

Carbon Monoxide and the Potential for Prebiotic Chemistry on Habitable Planets Around Main Sequence M Stars

NASA Technical Reports Server (NTRS)

Nava-Sedeno, J. Manik; Ortiz-Cervantes, Adrian; Segura, Antigona; Domagal-Goldman, Shawn D.

2016-01-01

Lifeless planets with CO2 atmospheres produce CO by CO2 photolysis. On planets around M dwarfs, CO is a long-lived atmospheric compound, as long as UV emission due to the stars chromospheric activity lasts, and the sink of CO and O2 in seawater is small compared to its atmospheric production. Atmospheres containing reduced compounds, like CO, may undergo further energetic and chemical processing to give rise to organic compounds of potential importance for the origin of life. We calculated the yield of organic compounds from CO2-rich atmospheres of planets orbiting M dwarf stars, which were previously simulated by Domagal- Goldman et al. (2014) and Harman et al. (2015), by cosmic rays and lightning using results of experiments by Miyakawaet al. (2002) and Schlesinger and Miller (1983a, 1983b). Stellar protons from active stars may be important energy sources for abiotic synthesis and increase production rates of biological compounds by at least 2 orders of magnitude compared to cosmic rays. Simple compounds such as HCN and H2CO are more readily synthesized than more complex ones, such as amino acids and uracil (considered here as an example), resulting in higher yields for the former and lower yields for the latter. Electric discharges are most efficient when a reducing atmosphere is present. Nonetheless, atmospheres with high quantities of CO2 are capable of producing higher amounts of prebiotic compounds, given that CO is constantly produced in the atmosphere. Our results further support planetary systems around M dwarf stars as candidates for supporting life or its origin.

Carbon dioxide partial pressure and 13C content of north temperate and boreal lakes at spring ice melt

USGS Publications Warehouse

Striegl, Robert G.; Kortelainen, Pirkko; Chanton, J.P.; Wickland, K.P.; Bugna, G.C.; Rantakari, M.

2001-01-01

Carbon dioxide (CO2) accumulates under lake ice in winter and degasses to the atmosphere after ice melt. This large springtime CO2 pulse is not typically considered in surface-atmosphere flux estimates, because most field studies have not sampled through ice during late winter. Measured CO2 partial pressure (pCO2) of lake surface water ranged from 8.6 to 4,290 Pa (85-4,230 ??atm) in 234 north temperate and boreal lakes prior to ice melt during 1998 and 1999. Only four lakes had surface pCO2 less than or equal to atmospheric pCO2, whereas 75% had pCO2 >5 times atmospheric. The ??13CDIC (DIC = ??CO2) of 142 of the lakes ranged from -26.28??? to +0.95.???. Lakes with the greatest pCO2 also had the lightest ??13CDIC, which indicates respiration as their primary CO2 source. Finnish lakes that received large amounts of dissolved organic carbon from surrounding peatlands had the greatest pCO2. Lakes set in noncarbonate till and bedrock in Minnesota and Wisconsin had the smallest pCO2 and the heaviest ??13CDIC, which indicates atmospheric and/or mineral sources of C for those lakes. Potential emissions for the period after ice melt were 2.36 ?? 1.44 mol CO2 m-2 for lakes with average pCO2 values and were as large as 13.7 ?? 8.4 mol CO2 m-2 for lakes with high pCO2 values.

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

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

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

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

Role of Atmospheric CO2 in the Ice Ages (Invited)

NASA Astrophysics Data System (ADS)

Toggweiler, J. R.

2010-12-01

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

Causes and Implications of Persistent Atmospheric Carbon Dioxide Biases in Earth System Models

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

Hoffman, Forrest M; Randerson, James T.; Arora, Vivek K.

The strength of feedbacks between a changing climate and future CO2 concentrations are uncertain and difficult to predict using Earth System Models (ESMs). We analyzed emission-driven simulations--in which atmospheric CO2 levels were computed prognostically--for historical (1850-2005) and future periods (RCP 8.5 for 2006-2100) produced by 15 ESMs for the Fifth Phase of the Coupled Model Intercomparison Project (CMIP5). Comparison of ESM prognostic atmospheric CO2 over the historical period with observations indicated that ESMs, on average, had a small positive bias in predictions of contemporary atmospheric CO2. Weak ocean carbon uptake in many ESMs contributed to this bias, based on comparisonsmore » with observations of ocean and atmospheric anthropogenic carbon inventories. We found a significant linear relationship between contemporary atmospheric CO2 biases and future CO2 levels for the multi-model ensemble. We used this relationship to create a contemporary CO2 tuned model (CCTM) estimate of the atmospheric CO2 trajectory for the 21st century. The CCTM yielded CO2 estimates of 600 {plus minus} 14 ppm at 2060 and 947 {plus minus} 35 ppm at 2100, which were 21 ppm and 32 ppm below the multi-model mean during these two time periods. Using this emergent constraint approach, the likely ranges of future atmospheric CO2, CO2-induced radiative forcing, and CO2-induced temperature increases for the RCP 8.5 scenario were considerably narrowed compared to estimates from the full ESM ensemble. Our analysis provided evidence that much of the model-to-model variation in projected CO2 during the 21st century was tied to biases that existed during the observational era, and that model differences in the representation of concentration-carbon feedbacks and other slowly changing carbon cycle processes appear to be the primary driver of this variability. By improving models to more closely match the long-term time series of CO2 from Mauna Loa, our analysis suggests uncertainties in future climate projections can be reduced.« less

Causes and implications of persistent atmospheric carbon dioxide biases in Earth System Models

NASA Astrophysics Data System (ADS)

Hoffman, F. M.; Randerson, J. T.; Arora, V. K.; Bao, Q.; Cadule, P.; Ji, D.; Jones, C. D.; Kawamiya, M.; Khatiwala, S.; Lindsay, K.; Obata, A.; Shevliakova, E.; Six, K. D.; Tjiputra, J. F.; Volodin, E. M.; Wu, T.

2014-02-01

The strength of feedbacks between a changing climate and future CO2 concentrations is uncertain and difficult to predict using Earth System Models (ESMs). We analyzed emission-driven simulations—in which atmospheric CO2levels were computed prognostically—for historical (1850-2005) and future periods (Representative Concentration Pathway (RCP) 8.5 for 2006-2100) produced by 15 ESMs for the Fifth Phase of the Coupled Model Intercomparison Project (CMIP5). Comparison of ESM prognostic atmospheric CO2 over the historical period with observations indicated that ESMs, on average, had a small positive bias in predictions of contemporary atmospheric CO2. Weak ocean carbon uptake in many ESMs contributed to this bias, based on comparisons with observations of ocean and atmospheric anthropogenic carbon inventories. We found a significant linear relationship between contemporary atmospheric CO2 biases and future CO2levels for the multimodel ensemble. We used this relationship to create a contemporary CO2 tuned model (CCTM) estimate of the atmospheric CO2 trajectory for the 21st century. The CCTM yielded CO2estimates of 600±14 ppm at 2060 and 947±35 ppm at 2100, which were 21 ppm and 32 ppm below the multimodel mean during these two time periods. Using this emergent constraint approach, the likely ranges of future atmospheric CO2, CO2-induced radiative forcing, and CO2-induced temperature increases for the RCP 8.5 scenario were considerably narrowed compared to estimates from the full ESM ensemble. Our analysis provided evidence that much of the model-to-model variation in projected CO2 during the 21st century was tied to biases that existed during the observational era and that model differences in the representation of concentration-carbon feedbacks and other slowly changing carbon cycle processes appear to be the primary driver of this variability. By improving models to more closely match the long-term time series of CO2from Mauna Loa, our analysis suggests that uncertainties in future climate projections can be reduced.

CO2 greenhouse in the early martian atmosphere: SO2 inhibits condensation

NASA Technical Reports Server (NTRS)

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

1997-01-01

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

Controlled-atmosphere effects on postharvest quality and antioxidant activity of cranberry fruits.

PubMed

Gunes, Gurbuz; Liu, Rui Hai; Watkins, Christopher B

2002-10-09

The effects of controlled-atmosphere (CA) storage on the firmness, respiration rate, quality, weight loss, total phenolics and flavonoids contents, and total antioxidant activities of the Pilgrim and Stevens cultivars of cranberries (Vaccinium macrocarpon Aiton) have been studied during storage in atmospheres of 2, 21, and 70% O(2) with 0, 15, and 30% CO(2) (balance N(2)); and 100% N(2) at 3 degrees C. Elevated CO(2) concentrations decreased bruising, physiological breakdown, and decay of berries, thereby reducing fruit losses. Respiration and weight loss of fruits decreased, but fruit softening increased, at higher CO(2) concentrations. Accumulations of acetaldehyde, ethanol, and ethyl acetate varied by cultivar and storage atmosphere but were generally highest in the 2 and 70% O(2) and 100% N(2) atmospheres and increased in response to elevated CO(2) concentrations. Overall, the 30% CO(2) plus 21% O(2) atmosphere appeared optimal for the storage of cranberries. Sensory analysis is required, however, to confirm that accumulations of fermentation products at this atmosphere are acceptable for consumers. Stevens fruits had a higher phenolics content and total antioxidant activity than Pilgrim fruits. The storage atmosphere did not affect the content of total phenolics or flavonoids. However, the total antioxidant activity of the fruits increased overall by about 45% in fruits stored in air. This increase was prevented by storage in 30% CO(2) plus 21% O(2).

Transmission of atmospherically derived trace elements through an undeveloped, forested Maryland watershed

USGS Publications Warehouse

Scudlark, J.R.; Rice, Karen C.; Conko, Kathryn M.; Bricker, Owen P.; Church, T.M.

2005-01-01

The transmission of atmospherically derived trace elements (Al, As, Cd, Cr, Cu, Fe, Mn, Ni, Pb, Se, and Zn) was evaluated in a small, undeveloped, forested watershed located in north-central Maryland. Atmospheric input was determined for wet-only and vegetative throughfall components. Annual throughfall fluxes were significantly enriched over incident precipitation for most elements, although some elements exhibited evidence of canopy release (Mn) or preferential uptake (As, Cr, and Se). Stream export was gauged based on systematic sampling under varied flow regimes. Particle loading appears to contribute significantly to watershed export (> 10%) for only As, Pb, and Fe, and then only during large precipitation/runoff events. The degree of watershed transmission for each trace element was evaluated based on a comparison of total, net atmospheric input (throughfall) to stream export over an annual hydrologic cycle. This comparison indicates that the atmospheric input of some elements (Al, Cd, Ni, Zn) is effectively transmitted through the watershed, but other elements (Pb, As, Se, Fe, Cr, Cu) appear to be strongly sequestered, in the respective orders noted. Results suggest that precipitation and subsequent soil pH are the primary factors that determine the mobility of sequestered trace element phases.To further resolve primary atmospheric and secondary weathering components, the geochemical model NETPATH was applied. Results indicate that minerals dissolved include chlorite, plagioclase feldspar, epidote, and potassium feldspar; phases formed were kaolinite, pyrite, and silica. The model also indicates that weathering processes contribute negligible amounts of trace elements to stream export, indicative of the unreactive orthoquartzite bedrock lithology underlying the watershed. Thus, the stream export of trace elements primarily reflects atmospheric deposition to the local watershed.

Uncertainty Quantification and Assessment of CO2 Leakage in Groundwater Aquifers

NASA Astrophysics Data System (ADS)

Carroll, S.; Mansoor, K.; Sun, Y.; Jones, E.

2011-12-01

Complexity of subsurface aquifers and the geochemical reactions that control drinking water compositions complicate our ability to estimate the impact of leaking CO2 on groundwater quality. We combined lithologic field data from the High Plains Aquifer, numerical simulations, and uncertainty quantification analysis to assess the role of aquifer heterogeneity and physical transport on the extent of CO2 impacted plume over a 100-year period. The High Plains aquifer is a major aquifer over much of the central United States where CO2 may be sequestered in depleted oil and gas reservoirs or deep saline formations. Input parameters considered included, aquifer heterogeneity, permeability, porosity, regional groundwater flow, CO2 and TDS leakage rates over time, and the number of leakage source points. Sensitivity analysis suggest that variations in sand and clay permeability, correlation lengths, van Genuchten parameters, and CO2 leakage rate have the greatest impact on impacted volume or maximum distance from the leak source. A key finding is that relative sensitivity of the parameters changes over the 100-year period. Reduced order models developed from regression of the numerical simulations show that volume of the CO2-impacted aquifer increases over time with 2 order of magnitude variance.

Poromechanical response of naturally fractured sorbing media

NASA Astrophysics Data System (ADS)

Kumar, Hemant

The injection of CO2 in coal seams has been utilized for enhanced gas recovery and potential CO2 sequestration in unmineable coal seams. It is advantageous because as it enhances the production and significant volumes of CO2 may be stored simultaneously. The key issues for enhanced gas recovery and geologic sequestration of CO2 include (1) Injectivity prediction: The chemical and physical processes initiated by the injection of CO2 in the coal seam leads to permeability/porosity changes (2) Up scaling: Development of full scale coupled reservoir model which may predict the enhanced production, associated permeability changes and quantity of sequestered CO2. (3) Reservoir Stimulation: The coalbeds are often fractured and proppants are placed into the fractures to prevent the permeability reduction but the permeability evolution in such cases is poorly understood. These issues are largely governed by dynamic coupling of adsorption, fluid exchange, transport, water content, stress regime, fracture geometry and physiomechanical changes in coals which are triggered by CO 2 injection. The understanding of complex interactions in coal has been investigated through laboratory experiments and full reservoir scale models are developed to answer key issues. (Abstract shortened by ProQuest.).

TES/Aura L2 Carbon Dioxide (CO2) Nadir V7 (TL2CO2N)

Atmospheric Science Data Center

2018-01-18

... TES/Aura L2 Carbon Dioxide (CO2) Nadir (TL2CO2N) News:  TES News Join TES News List Project ... TES Order Tool Parameters:  Earth Science Atmosphere Atmospheric Chemistry/Carbon and Hydrocarbon Compounds ...

Primary, secondary, and tertiary amines for CO2 capture: designing for mesoporous CO2 adsorbents.

PubMed

Ko, Young Gun; Shin, Seung Su; Choi, Ung Su

2011-09-15

CO(2) emissions, from fossil-fuel-burning power plants, the breathing, etc., influence the global worming on large scale and the man's work efficiency on small scale. The reversible capture of CO(2) is a prominent feature of CO(2) organic-inorganic hybrid adsorbent to sequester CO(2). Herein, (3-aminopropyl) trimethoxysilane (APTMS), [3-(methylamino)propyl] trimethoxysilane (MAPTMS), and [3-(diethylamino) propyl] trimethoxysilane (DEAPTMS) are immobilized on highly ordered mesoporous silicas (SBA-15) to catch CO(2) as primary, secondary, and tertiary aminosilica adsorbents. X-ray photoelectron spectroscopy was used to analyze the immobilized APTMS, MAPTMS, and DEAPTMS on the SBA-15. We report an interesting discovery that the CO(2) adsorption and desorption on the adsorbent depend on the amine type of the aminosilica adsorbent. The adsorbed CO(2) was easily desorbed from the adsorbent with the low energy consumption in the order of tertiary, secondary, and primary amino-adsorbents while the adsorption amount and the bonding-affinity increased in the reverse order. The effectiveness of amino-functionalized (1(o), 2(o), and 3(o) amines) SBA-15s as a CO(2) capturing agent was investigated in terms of adsorption capacity, adsorption-desorption kinetics, and thermodynamics. This work demonstrates apt amine types to catch CO(2) and regenerate the adsorbent, which may open new avenues to designing "CO(2) basket". Copyright © 2011. Published by Elsevier Inc.

Carbon sequestration to mitigate climate change

USGS Publications Warehouse

Sundquist, Eric; Burruss, Robert; Faulkner, Stephen; Gleason, Robert; Harden, Jennifer; Kharaka, Yousif; Tieszen, Larry; Waldrop, Mark

2008-01-01

Human activities, especially the burning of fossil fuels such as coal, oil, and gas, have caused a substantial increase in the concentration of carbon dioxide (CO2) in the atmosphere. This increase in atmospheric CO2 - from about 280 to more than 380 parts per million (ppm) over the last 250 years - is causing measurable global warming. Potential adverse impacts include sea-level rise; increased frequency and intensity of wildfires, floods, droughts, and tropical storms; changes in the amount, timing, and distribution of rain, snow, and runoff; and disturbance of coastal marine and other ecosystems. Rising atmospheric CO2 is also increasing the absorption of CO2 by seawater, causing the ocean to become more acidic, with potentially disruptive effects on marine plankton and coral reefs. Technically and economically feasible strategies are needed to mitigate the consequences of increased atmospheric CO2. The United States needs scientific information to develop ways to reduce human-caused CO2 emissions and to remove CO2 from the atmosphere.

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

NASA Astrophysics Data System (ADS)

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

2018-06-01

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

Monitoring Atmospheric CO2 From Space: Challenge & Approach

NASA Technical Reports Server (NTRS)

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

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

PubMed Central

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

2015-01-01

The change in ancient atmospheric CO2 concentrations provides important clues for understanding the relationship between the atmospheric CO2 concentration and global temperature. However, the lack of CO2 evolution curves estimated from a single terrestrial proxy prevents the understanding of climatic and environmental impacts due to variations in data. Thus, based on the stomatal index of fossilized Metasequoia needles, we reconstructed a history of atmospheric CO2 concentrations from middle Miocene to late Early Pleistocene when the climate changed dramatically. According to this research, atmospheric CO2 concentration was stabile around 330–350 ppmv in the middle and late Miocene, then it decreased to 278–284 ppmv during the Late Pliocene and to 277–279 ppmv during the Early Pleistocene, which was almost the same range as in preindustrial time. According to former research, this is a time when global temperature decreased sharply. Our results also indicated that from middle Miocene to Pleistocene, global CO2 level decreased by more than 50 ppmv, which may suggest that CO2 decrease and temperature decrease are coupled. PMID:26154449

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

PubMed

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

2015-01-01

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

Microbial Growth under Supercritical CO2

PubMed Central

Peet, Kyle C.; Freedman, Adam J. E.; Hernandez, Hector H.; Britto, Vanya; Boreham, Chris; Ajo-Franklin, Jonathan B.

2015-01-01

Growth of microorganisms in environments containing CO2 above its critical point is unexpected due to a combination of deleterious effects, including cytoplasmic acidification and membrane destabilization. Thus, supercritical CO2 (scCO2) is generally regarded as a sterilizing agent. We report isolation of bacteria from three sites targeted for geologic carbon dioxide sequestration (GCS) that are capable of growth in pressurized bioreactors containing scCO2. Analysis of 16S rRNA genes from scCO2 enrichment cultures revealed microbial assemblages of varied complexity, including representatives of the genus Bacillus. Propagation of enrichment cultures under scCO2 headspace led to isolation of six strains corresponding to Bacillus cereus, Bacillus subterraneus, Bacillus amyloliquefaciens, Bacillus safensis, and Bacillus megaterium. Isolates are spore-forming, facultative anaerobes and capable of germination and growth under an scCO2 headspace. In addition to these isolates, several Bacillus type strains grew under scCO2, suggesting that this may be a shared feature of spore-forming Bacillus spp. Our results provide direct evidence of microbial activity at the interface between scCO2 and an aqueous phase. Since microbial activity can influence the key mechanisms for permanent storage of sequestered CO2 (i.e., structural, residual, solubility, and mineral trapping), our work suggests that during GCS microorganisms may grow and catalyze biological reactions that influence the fate and transport of CO2 in the deep subsurface. PMID:25681188

Extracellular hemoglobin: the case of a friend turned foe

PubMed Central

Quaye, Isaac K.

2015-01-01

Hemoglobin (Hb) is a highly conserved molecule present in all life forms and functionally tied to the complexity of aerobic organisms on earth in utilizing oxygen from the atmosphere and delivering to cells and tissues. This primary function sustains the energy requirements of cells and maintains cellular homeostasis. Decades of intensive research has presented a paradigm shift that shows how the molecule also functions to facilitate smooth oxygen delivery through the cardiovascular system for cellular bioenergetic homeostasis and signaling for cell function and defense. These roles are particularly highlighted in the binding of Hb to gaseous molecules carbon dioxide (CO2), nitric oxide (NO) and carbon monoxide (CO), while also serving indirectly or directly as sources of these signaling molecules. The functional activities impacted by Hb outside of bioenergetics homeostasis, include fertilization, signaling functions, modulation of inflammatory responses for defense and cell viability. These activities are efficiently executed while Hb is sequestered safely within the confines of the red blood cell (rbc). Outside of rbc confines, Hb disaggregates and becomes a danger molecule to cell survival. In these perpectives, Hb function is broadly dichotomous, either a friend in its natural environment providing and facilitating the means for cell function or foe when dislocated from its habitat under stress or pathological condition disrupting cell function. The review presents insights into how this dichotomy in function manifests. PMID:25941490

Programmable pH buffers

DOEpatents

Gough, Dara Van; Huber, Dale L.; Bunker, Bruce C.; Roberts, Mark E.

2017-01-24

A programmable pH buffer comprises a copolymer that changes pK.sub.a at a lower critical solution temperature (LCST) in water. The copolymer comprises a thermally programmable polymer that undergoes a hydrophobic-to-hydrophilic phase change at the LCST and an electrolytic polymer that exhibits acid-base properties that are responsive to the phase change. The programmable pH buffer can be used to sequester CO.sub.2 into water.

Monthly Atmospheric 13C/12C Isotopic Ratios for 11 SIO Stations (1977-2008)

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

Keeling, R. F.; Piper, S. C.; Bollenbacher, A. F.

Stable isotopic measurements for atmospheric 13C/12C and 18O/16O at global sampling sites were initiated by Dr. C.D. Keeling and co-workers at Scripps Institution of Oceanography (SIO) in 1977. These isotopic measurements complement the continuing global atmospheric and oceanic CO2 measurements initiated by Keeling in 1957. This work is currently being continued under the direction of R.F. Keeling, who also runs a parallel program at SIO to measure changes in atmospheric O2 and Ar abundances (Scripps O2 Program). A more complete set of 13CO2 data is found online at http://scrippsco2.ucsd.edu/data/atmospheric_co2.html

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

NASA Astrophysics Data System (ADS)

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

2014-11-01

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

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

NASA Astrophysics Data System (ADS)

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

2014-11-01

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

Is there an Alternative for the Huge Impact-Generated Atmosphere?

NASA Astrophysics Data System (ADS)

Gerasimov, M. V.; Dikov, Y. P.; Yakovlev, O. I.; Wlotzka, F.

1998-01-01

The Earth's primordial atmosphere is considered to be the result of impact degassing during planetary accretion. Experiments on the decomposition of a serpentine and calcite during a shock wave loading showed that a rather efficient decomposition could be achieved beginning with the impact velocities that corresponded to escape velocities of a relatively small (about Moon-sized) planetary embryo. During further accumulation of planetary mass, the decomposition of serpentine and carbonates with the release of H2O and CO2 (gases considered to be the main product of impact degassing) into the primordial atmosphere was considered to be complete. The sink rate of H2O and CO2 from the primordial atmosphere was evaluated mainly as atmospheric impact erosion, thermal and EW-driven escape from the atmosphere, hydration and carboniza60n of surface minerals, dissolution of gases in magma ocean, loss of water for oxidation of Fe, etc. The growth of the atmosphere was considered to be a result of source and sink processes during each impact event. The rehydration of 100% of degassed material during an impact is considered to be an end effect when no hydrous atmosphere is formed. But even a small efficiency of impact degassing (the ratio of volatiles that remain in the atmosphere after an impact to the amount delivered by a planetesimal) was calculated to produce an abundant H2O-CO2 atmosphere. During a set of impact simulation experiments we have investigated the chemistry of volatiles and their interaction behavior with condensing silicates at conditions similar to impact vaporization. First, the experiments showed that the gas mixture was not limited only by H20 and CO2 during high-temperature vaporization of silicates, a wide variety of gases were formed, including oxides [SO2, CO2, CO (CO/CO2 approximately 1), H20] and reduced gas components (H2, H2S, CS2, COS, and hydrocarbons). Second, experiments on high-temperature vaporization of mafic and ultramafic rocks and minerals in water and/or CO2 containing atmospheres showed that condensing silicates provide intense trapping of water and/or CO2 during the hot stage of vapor cloud expansion. The amount of water trapped by formation of different hydroxides could be about 10 wt% of silicate mass. The trapping of atmospheric CO2 is proceeded by the formation of carbonates, carbides, hydrocarbons, and elemental C phases. Preliminary results indicate that Ni is also trapped by formation of -NO3, -H2N, and -CN phases. The maximum concentrations of trapped CO2 and N were measured up to 4 wt% and 0.1 wt% respectively. Trapping is efficient even at low partial gas pressures. Impact-induced trapping of atmospheric gases was not accounted for by theoretical models, but it seems to be an efficient process controlling the atmospheric mass. The ratio of volatiles added to the atmosphere after an impact to the amount delivered by a planetesimal can only be positive but sufficiently negative as well. During the impact of a planetesimal analogous to an ordinary chondrite on the growing Earth with a dense atmosphere, the removal of gases from the atmosphere seems to be more probable as a result of release and trapping processes. The capacity of the sink buffer exceeds the whole planetary volatile inventory. The trapping efficiency of gases inside the vapor plume suggests a model for the formation of a primordial atmosphere of moderate density.

Effects of Elevated CO2 Concentration on Photosynthesis and Respiration of Populus Deltodies

NASA Technical Reports Server (NTRS)

Anderson, Angela M.

1998-01-01

To determine how increased atmospheric CO2 will affect the physiology of cottonwood trees, cuttings of the cloned Populus deltodies [cottonwood] were grown in open-top chambers containing ambient or elevated CO2 concentration. The control treatment was maintained at ambient Biosphere 2 atmospheric CO2 (c. 450 +/- 50 micro l/l), and elevated CO2 treatment was maintained at approximately double ambient Biosphere 2 atmospheric CO2 (c. 1000 +/- 50 micro l/l). The effects of elevated CO2 on leaf photosynthesis, and stomatal conductance were measured. The cottonwoods exposed to CO2 enrichment showed no significant indication of photosynthetic down-regulation. There was no significant difference in the maximum assimilation rate between the treatment and the control (P less than 0.24). The CO2 enriched treatment showed a decreased stomatal conductance of 15% (P less than 0.03). The elevated CO2 concentrated atmosphere had an effect on the respiration rates of the plants; the compensation point of the treatment was on average 13% higher than the control (P less than 0.01).

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

NASA Astrophysics Data System (ADS)

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

2017-12-01

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

Uptake of atmospheric carbon dioxide into silk fiber by silkworms.

PubMed

Magoshi, Jun; Tanaka, Toshihisa; Sasaki, Haruto; Kobayashi, Masatoshi; Magoshi, Yoshiko; Tsuda, Hidetoshi; Becker, Mary A; Inoue, Shun-ichi; Ishimaru, Ken

2003-01-01

The relation between the uptake of atmospheric CO(2) and insect's production of silk fiber has not yet been reported. Here, we provide the first quantitative demonstrations that four species of silkworms (Bombyx mori, Samia cynthia ricini, Antheraea pernyi, and Antheraea yamamai) and a silk-producing spider (Nephila clavata) incorporate atmospheric CO(2) into their silk fibers. The abundance of (13)C incorporated from the environment was determined by mass spectrometry and (13)C NMR measurements. Atmospheric CO(2) was incorporated into the silk fibers in the carbonyl groups of alanine, aspartic acid, serine, and glycine and the C(gamma) of aspartic acid. We show a simple model for the uptake of atmospheric CO(2) by silkworms. These results will demonstrate that silkworm has incorporated atmospheric CO(2) into silk fiber via the TCA cycle; however, the magnitude of uptake into the silk fibers is smaller than that consumed by the photosynthesis in trees and coral reefs.

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

NASA Astrophysics Data System (ADS)

Cowling, Sharon A.; Sykes, Martin T.

1999-09-01

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

Atmospheric Carbon Dioxide and the Global Carbon Cycle: The Key Uncertainties

DOE R&D Accomplishments Database

Peng, T. H.; Post, W. M.; DeAngelis, D. L.; Dale, V. H.; Farrell, M. P.

1987-12-01

The biogeochemical cycling of carbon between its sources and sinks determines the rate of increase in atmospheric CO{sub 2} concentrations. The observed increase in atmospheric CO{sub 2} content is less than the estimated release from fossil fuel consumption and deforestation. This discrepancy can be explained by interactions between the atmosphere and other global carbon reservoirs such as the oceans, and the terrestrial biosphere including soils. Undoubtedly, the oceans have been the most important sinks for CO{sub 2} produced by man. But, the physical, chemical, and biological processes of oceans are complex and, therefore, credible estimates of CO{sub 2} uptake can probably only come from mathematical models. Unfortunately, one- and two-dimensional ocean models do not allow for enough CO{sub 2} uptake to accurately account for known releases. Thus, they produce higher concentrations of atmospheric CO{sub 2} than was historically the case. More complex three-dimensional models, while currently being developed, may make better use of existing tracer data than do one- and two-dimensional models and will also incorporate climate feedback effects to provide a more realistic view of ocean dynamics and CO{sub 2} fluxes. The instability of current models to estimate accurately oceanic uptake of CO{sub 2} creates one of the key uncertainties in predictions of atmospheric CO{sub 2} increases and climate responses over the next 100 to 200 years.

Net uptake of atmospheric CO2 by coastal submerged aquatic vegetation

PubMed Central

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

2014-01-01

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

Atmospheric measurement of point source fossil fuel CO2 emissions

NASA Astrophysics Data System (ADS)

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

2013-11-01

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

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

PubMed

Xu, Ming

2015-07-20

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

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

NASA Technical Reports Server (NTRS)

Schlesinger, G.; Miller, S. L.

1983-01-01

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

Modeling Microalgal Biosediment Formation Based on Attenuated Total Reflection Fourier Transform Infrared (ATR FT-IR) Monitoring.

PubMed

Ogburn, Zachary L; Vogt, Frank

2018-03-01

With increasing amounts of anthropogenic pollutants being released into ecosystems, it becomes ever more important to understand their fate and interactions with living organisms. Microalgae play an important ecological role as they are ubiquitous in marine environments and sequester inorganic pollutants which they transform into organic biomass. Of particular interest in this study is their role as a sink for atmospheric CO 2 , a greenhouse gas, and nitrate, one cause of harmful algal blooms. Novel chemometric hard-modeling methodologies have been developed for interpreting phytoplankton's chemical and physiological adaptations to changes in their growing environment. These methodologies will facilitate investigations of environmental impacts of anthropogenic pollutants on chemical and physiological properties of marine microalgae (here: Nannochloropsis oculata). It has been demonstrated that attenuated total reflection Fourier transform infrared (ATR FT-IR) spectroscopy can gain insights into both and this study only focuses on the latter. From time-series of spectra, the rate of microalgal biomass settling on top of a horizontal ATR element is derived which reflects several of phytoplankton's physiological parameters such as growth rate, cell concentrations, cell size, and buoyancy. In order to assess environmental impacts on such parameters, microalgae cultures were grown under 25 different chemical scenarios covering 200-600 ppm atmospheric CO 2 and 0.35-0.75 mM dissolved NO 3 - . After recording time-series of ATR FT-IR spectra, a multivariate curve resolution-alternating least squares (MCR-ALS) algorithm extracted spectroscopic and time profiles from each data set. From the time profiles, it was found that in the considered concentration ranges only NO 3 - has an impact on the cells' physiological properties. In particular, the cultures' growth rate has been influenced by the ambient chemical conditions. Thus, the presented spectroscopic + chemometric methodology enables investigating the link between chemical conditions in a marine ecosystem and their consequences for phytoplankton living in it.

Improving city forests through assessment, modelling and monitoring

Treesearch

D.J. Nowak

2018-01-01

Urban and peri-urban forests produce numerous benefits for society. These include moderating the climate; reducing energy use in buildings; sequestering atmospheric carbon dioxide; improving air and water quality; mitigating rainfall run-off and flooding; providing an aesthetic environment and recreational opportunities; enhancing human health and social well-being;...

Biochar and soil properties affecting microbial transport through biochar-amended soils

USDA-ARS?s Scientific Manuscript database

The incorporation of biochar into soils has been proposed as a means to sequester carbon from the atmosphere. An added environmental benefit is that biochar has also been shown to increase soil retention of nutrients, heavy metals, and pesticides. We have recently conducted a series of experiments t...

Forest carbon calculators: a review for managers, policymakers, and educators

Treesearch

Harold S.J. Zald; Thomas A. Spies; Mark E. Harmon; Mark J. Twery

2016-01-01

Forests play a critical role sequestering atmospheric carbon dioxide, partially offsetting greenhouse gas emissions, and thereby mitigating climate change. Forest management, natural disturbances, and the fate of carbon in wood products strongly influence carbon sequestration and emissions in the forest sector. Government policies, carbon offset and trading programs,...

The challenge of making ozone risk assessment for forest trees more mechanistic

USDA-ARS?s Scientific Manuscript database

In the upcoming decades, the earth’s atmosphere will contain increasing levels of carbon dioxide and possibly tropospheric ozone. The latter constitute a risk for vegetation, including forest ecosystems, counteracting the ability to sequester carbon. In view of climate change, the need increases f...

Carbon Monoxide and the Potential for Prebiotic Chemistry on Habitable Planets around Main Sequence M Stars.

PubMed

Nava-Sedeño, J Manik; Ortiz-Cervantes, Adrian; Segura, Antígona; Domagal-Goldman, Shawn D

2016-10-04

Lifeless planets with CO 2 atmospheres produce CO by CO 2 photolysis. On planets around M dwarfs, CO is a long-lived atmospheric compound, as long as UV emission due to the star's chromospheric activity lasts, and the sink of CO and O 2 in seawater is small compared to its atmospheric production. Atmospheres containing reduced compounds, like CO, may undergo further energetic and chemical processing to give rise to organic compounds of potential importance for the origin of life. We calculated the yield of organic compounds from CO 2 -rich atmospheres of planets orbiting M dwarf stars, which were previously simulated by Domagal-Goldman et al. (2014) and Harman et al. (2015), by cosmic rays and lightning using results of experiments by Miyakawa et al. (2002) and Schlesinger and Miller ( 1983a , 1983b ). Stellar protons from active stars may be important energy sources for abiotic synthesis and increase production rates of biological compounds by at least 2 orders of magnitude compared to cosmic rays. Simple compounds such as HCN and H 2 CO are more readily synthesized than more complex ones, such as amino acids and uracil (considered here as an example), resulting in higher yields for the former and lower yields for the latter. Electric discharges are most efficient when a reducing atmosphere is present. Nonetheless, atmospheres with high quantities of CO 2 are capable of producing higher amounts of prebiotic compounds, given that CO is constantly produced in the atmosphere. Our results further support planetary systems around M dwarf stars as candidates for supporting life or its origin. Key Words: Prebiotic chemistry-M dwarfs-Habitable planets-Cosmic rays-Lightning-Stellar activity. Astrobiology 16, 744-754.

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

NASA Astrophysics Data System (ADS)

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

2017-12-01

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

Seal assessment and estimated storage capacities of a targeted CO2 reservoir based on new displacement pressures in SW Wyoming, U.S.A.

NASA Astrophysics Data System (ADS)

Spaeth, Lynsey; Campbell-Stone, Erin; Lynds, Ranie; Frost, Carol; McLaughlin, J. Fred

2013-04-01

Carbon capture and storage locations are being investigated throughout the state of Wyoming, USA, in preparation for sequestration of greenhouse gases. At potential storage sites, confining units must be identified that are capable of ensuring stored carbon dioxide remains in place at depth. Previous fluid inclusion volatile work indicates that Triassic formations in southwestern Wyoming act as a confining system on the Rock Springs uplift (RSU). An investigation of the Triassic Dinwoody Formation using mercury capillary entry pressure was conducted to calculate column height potential for CO2 sequestration on the RSU. A stratigraphic test well drilled on the RSU recovered 27.4 meters of core from the Dinwoody Formation. It is dominantly a brownish-red, very fine-grained sandy and micaceous siltstone with minor layers of thin mudstone and minor amounts of anhydrite. Four samples were taken from this core for mercury injection capillary pressure (MICP) analysis. During MICP analysis, mercury is injected into the sample over a range of pressures increased in steps. Only when sufficient pressure is applied will the mercury penetrate into the pore system and at this pressure a confining system will begin to leak. The mercury entry pressures for the Dinwoody samples range from 6.58 to18.85 megapascals and were converted to entry pressures for brine/CO2 systems. Previous simulations indicate that sequestering commercial quantities of CO2 (5-15 megatons CO2/year) over the course of 50 years can be accommodated at the RSU. Determination of the total possible capacity requires knowledge of the column height, i.e. the vertical thickness of CO2 that can be safely injected without caprock failure. Using converted pressures for brine/CO2 systems, the interfacial tensions of CO2, water, and substrate, as well as the densities of CO2 and brine, column heights were calculated for the RSU. It has been suggested by other research that supercritical CO2 and brine may behave as a single wetting phase at elevated pressures and temperatures, resulting in an interfacial tension of 0 milliNewton/meter. Under these conditions the pore throat radius of sealing units is assumed to be the principle inhibitor to flow through the seal. Experimental data indicate pore throat radii range from 39.2 to 113.5 nanometers in the confining system, and preliminary column height calculations indicate that, depending on the size of the plume, reservoir thickness will most likely be the limiting factor to the amount of CO2 that can be sequestered rather than the column height.

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

NASA Astrophysics Data System (ADS)

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

2016-12-01

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

Exploring the low friction of diamond-like carbon films in carbon dioxide atmosphere by experiments and first-principles calculations

NASA Astrophysics Data System (ADS)

Huo, Lei; Wang, Shunhua; Pu, Jibin; Sun, Junhui; Lu, Zhibin; Ju, Pengfei; Wang, Liping

2018-04-01

The friction behavior and the mechanism of DLC films in CO2 atmosphere are rarely explored, which is a significant obstacle for the potential practical application of DLC films in primarily CO2 environment. Here, the experiments and first-principles calculations are performed to simultaneously investigate this theme. We find that DLC films in CO2 atmosphere exhibit astoundingly low friction coefficient compared with in ambient air and vacuum atmospheres. The XPS and Raman spectrums demonstrate the possibly activation of CO2 molecule in the shearing interfaces, which may be critical for the low friction of DLC films in CO2 atmosphere. The calculated results reveal that the lactone groups can easily form during the horizontally chemisorption of CO2 molecule on the DLC surface, which is energetic and is a favorable process under the interfacial stress. Because of the presence of the lone-pairs of the lactone group, the lactone-terminated surfaces appear to be responsible for the low friction of DLC films in CO2 atmosphere. The studies may open up the possibility for DLC films usage in Mars applications.

Evaluation of simulated biospheric carbon dioxide fluxes and atmospheric concentrations using global in situ observations

NASA Astrophysics Data System (ADS)

Philip, S.; Johnson, M. S.; Potter, C. S.; Genovese, V. B.

2016-12-01

Atmospheric mixing ratios of carbon dioxide (CO2) are largely controlled by anthropogenic emission sources and biospheric sources/sinks. Global biospheric fluxes of CO2 are controlled by complex processes facilitating the exchange of carbon between terrestrial ecosystems and the atmosphere. These processes which play a key role in these terrestrial ecosystem-atmosphere carbon exchanges are currently not fully understood, resulting in large uncertainties in the quantification of biospheric CO2 fluxes. Current models with these inherent deficiencies have difficulties simulating the global carbon cycle with high accuracy. We are developing a new modeling platform, GEOS-Chem-CASA by integrating the year-specific NASA-CASA (National Aeronautics and Space Administration - Carnegie Ames Stanford Approach) biosphere model with the GEOS-Chem (Goddard Earth Observation System-Chemistry) chemical transport model to improve the simulation of atmosphere-terrestrial ecosystem carbon exchange. We use NASA-CASA to explicitly represent the exchange of CO2 between terrestrial ecosystem and atmosphere by replacing the baseline GEOS-Chem land net CO2 flux and forest biomass burning CO2 emissions. We will present the estimation and evaluation of these "bottom-up" land CO2 fluxes, simulated atmospheric mixing ratios, and forest disturbance changes over the last decade. In addition, we will present our initial comparison of atmospheric column-mean dry air mole fraction of CO2 predicted by the model and those retrieved from NASA's OCO-2 (Orbiting Carbon Observatory-2) satellite instrument and model-predicted surface CO2 mixing ratios with global in situ observations. This evaluation is the first step necessary for our future work planned to constrain the estimates of biospheric carbon fluxes through "top-down" inverse modeling, which will improve our understanding of the processes controlling atmosphere-terrestrial ecosystem greenhouse gas exchanges, especially over regions which lack in situ observations.

B33C-0612: Evaluation of Simulated Biospheric Carbon Dioxide Fluxes and Atmospheric Concentrations Using Global in Situ Observations

NASA Technical Reports Server (NTRS)

Philip, Sajeev; Johnson, Matthew S.; Potter, Christopher S.; Genovese, Vanessa

2016-01-01

Atmospheric mixing ratios of carbon dioxide (CO2) are largely controlled by anthropogenic emission sources and biospheric sources/sinks. Global biospheric fluxes of CO2 are controlled by complex processes facilitating the exchange of carbon between terrestrial ecosystems and the atmosphere. These processes which play a key role in these terrestrial ecosystem-atmosphere carbon exchanges are currently not fully understood, resulting in large uncertainties in the quantification of biospheric CO2 fluxes. Current models with these inherent deficiencies have difficulties simulating the global carbon cycle with high accuracy. We are developing a new modeling platform, GEOS-Chem-CASA by integrating the year-specific NASA-CASA (National Aeronautics and Space Administration - Carnegie Ames Stanford Approach) biosphere model with the GEOS-Chem (Goddard Earth Observation System-Chemistry) chemical transport model to improve the simulation of atmosphere-terrestrial ecosystem carbon exchange. We use NASA-CASA to explicitly represent the exchange of CO2 between terrestrial ecosystem and atmosphere by replacing the baseline GEOS-Chem land net CO2 flux and forest biomass burning CO2 emissions. We will present the estimation and evaluation of these "bottom-up" land CO2 fluxes, simulated atmospheric mixing ratios, and forest disturbance changes over the last decade. In addition, we will present our initial comparison of atmospheric column-mean dry air mole fraction of CO2 predicted by the model and those retrieved from NASA's OCO-2 (Orbiting Carbon Observatory-2) satellite instrument and model-predicted surface CO2 mixing ratios with global in situ observations. This evaluation is the first step necessary for our future work planned to constrain the estimates of biospheric carbon fluxes through "top-down" inverse modeling, which will improve our understanding of the processes controlling atmosphere-terrestrial ecosystem greenhouse gas exchanges, especially over regions which lack in situ observations.

Mitigation of greenhouse gases emissions impact and their influence on terrestrial ecosystem.

NASA Astrophysics Data System (ADS)

Wójcik Oliveira, K.; Niedbała, G.

2018-05-01

Nowadays, one of the most important challenges faced by the humanity in the current century is the increasing temperature on Earth, caused by a growing emission of greenhouse gases into the atmosphere. Terrestrial ecosystems, as an important component of the carbon cycle, play an important role in the sequestration of carbon, which is a chance to improve the balance of greenhouse gases. Increasing CO2 absorption by terrestrial ecosystems is one way to reduce the atmospheric CO2 emissions. Sequestration of CO2 by terrestrial ecosystems is not yet fully utilized method of mitigating CO2 emission to the atmosphere. Terrestrial ecosystems, especially forests, are essential for the regulation of CO2 content in the atmosphere and more attention should be paid to seeking the natural processes of CO2 sequestration.

Cooling the Martian atmosphere: The spectral overlap of the C02 15 micrometers band and dust

NASA Technical Reports Server (NTRS)

Lindner, Bernhard Lee

1994-01-01

Careful consideration must be given to the simultaneous treatment of the radiative transfer of the CO2 15 micron band and dust calculations for the Martian winter polar region show that a simple sum of separately calculated CO2 cooling rates and dust cooling rates can easily result a 30 percent error in the net cooling particularly near the surface. CO2 and dust hinder each others ability to cool the atmosphere. Even during periods of low dust opacity, dust still reduces the efficacy of CO2 at cooling the atmosphere. At the other extreme, when dust storms occur, CO2 still significantly impedes the ability of dust to cool the atmosphere. Hence, both CO2 and dust must be considered in radiative transfer models.

Integration of CO2 Capture and Mineral Carbonation by Using Recyclable Ammonium Salts

PubMed Central

Wang, Xiaolong; Maroto-Valer, M Mercedes

2011-01-01

A new approach to capture and store CO2 by mineral carbonation using recyclable ammonium salts was studied. This process integrates CO2 capture with mineral carbonation by employing NH3, NH4HSO4, and NH4HCO3 in the capture, mineral dissolution, and carbonation steps, respectively. NH4HSO4 and NH3 can then be regenerated by thermal decomposition of (NH4)2SO4. The use of NH4HCO3 as the source of CO2 can avoid desorption and compression of CO2. The mass ratio of Mg/NH4HCO3/NH3 is the key factor controlling carbonation and the optimum ratio of 1:4:2 gives a conversion of Mg ions to hydromagnesite of 95.5 %. Thermogravimetric analysis studies indicated that the regeneration efficiency of NH4HSO4 and NH3 in this process is 95 %. The mass balance of the process shows that about 2.63 tonnes of serpentine, 0.12 tonnes of NH4HSO4, 7.48 tonnes of NH4HCO3, and 0.04 tonnes of NH3 are required to sequester 1 tonne of CO2 as hydromagnesite. PMID:21732542

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

NASA Astrophysics Data System (ADS)

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

2015-12-01

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

An analysis of the global spatial variability of column-averaged CO2 from SCIAMACHY and its implications for CO2 sources and sinks

USGS Publications Warehouse

Zhang, Zhen; Jiang, Hong; Liu, Jinxun; Zhang, Xiuying; Huang, Chunlin; Lu, Xuehe; Jin, Jiaxin; Zhou, Guomo

2014-01-01

Satellite observations of carbon dioxide (CO2) are important because of their potential for improving the scientific understanding of global carbon cycle processes and budgets. We present an analysis of the column-averaged dry air mole fractions of CO2 (denoted XCO2) of the Scanning Imaging Absorption Spectrometer for Atmospheric Cartography (SCIAMACHY) retrievals, which were derived from a satellite instrument with relatively long-term records (2003–2009) and with measurements sensitive to the near surface. The spatial-temporal distributions of remotely sensed XCO2 have significant spatial heterogeneity with about 6–8% variations (367–397 ppm) during 2003–2009, challenging the traditional view that the spatial heterogeneity of atmospheric CO2 is not significant enough (2 and surface CO2 were found for major ecosystems, with the exception of tropical forest. In addition, when compared with a simulated terrestrial carbon uptake from the Integrated Biosphere Simulator (IBIS) and the Emissions Database for Global Atmospheric Research (EDGAR) carbon emission inventory, the latitudinal gradient of XCO2 seasonal amplitude was influenced by the combined effect of terrestrial carbon uptake, carbon emission, and atmospheric transport, suggesting no direct implications for terrestrial carbon sinks. From the investigation of the growth rate of XCO2 we found that the increase of CO2 concentration was dominated by temperature in the northern hemisphere (20–90°N) and by precipitation in the southern hemisphere (20–90°S), with the major contribution to global average occurring in the northern hemisphere. These findings indicated that the satellite measurements of atmospheric CO2 improve not only the estimations of atmospheric inversion, but also the understanding of the terrestrial ecosystem carbon dynamics and its feedback to atmospheric CO2.

Characteristics of variations of climate change and atmospheric CO2 concentration at different time scales over the past 500 Ma

NASA Astrophysics Data System (ADS)

LIU, Z.; Huang, S. S. X. E. C.; Tang, X.

2015-12-01

It is generally believed that current global warming is due to the persistent rise of atmospheric greenhouse gas CO2. The consensus is based mostly on the observational data of past decades and the polar ice core records. To understand the relationship between climate change and atmospheric CO2, their behaviors over a longer interval at different time scales need to be appreciated. Here, we collect and analyze past 500 Ma records of atmospheric CO2 and temperature in six time periods, namely Phanerozoic, Cenozoic, middle Pleistocene, last deglaciation, past millennium, and recent decades. According to the carriers and time spans, we divide these records into three categories: 1.The millionaire and longer records from model calculation and paleosols/paleobotany proxies. Although the trends of both variables are generally consistent on this time scale, it is difficult to establish a clear causal relationship because of great uncertainties and low resolutions of both sets of data. 2.The orbital scale mainly from the polar ice core. High precise CO2 and temperature reconstructions allow for an examination of the possible role of atmospheric CO2 in the glacial-interglacial transformation. 3.The records at centennial and shorter time scales over the past millennium from ice, snow, and instrumental data. The past millennium records are most abundant and accurate, especially CO2 has been measured directly in recent decades. However, due to the difficulties in distinguishing the effect of CO2 from other factors, there are great uncertainties in the interpretation of climate change versus CO2. Overall, we come to the following conclusions:1.Paleoclimatic reconstructions show that both temperature and atmospheric CO2 have generally decreased over the past 500 Ma. However, there are no consistent sequential orders in the changes between these two variables. 2.The Earth's atmospheric CO2 has a drastic oscillation history. There were many high CO2 periods when the values were higher than 5000 ppm, and there are several low CO2 periods when the values dropped to less than 100 ppm. 3.According to global observational data, atmospheric CO2 has recently exceeded 400 ppm. Although there is no conclusive evidence that shows this value has a special significance, it is the highest since the last 800 ka, and rare over the Quaternary.

Positive feedback between increasing atmospheric CO2 and ecosystem productivity

NASA Astrophysics Data System (ADS)

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

2009-12-01

Increasing atmospheric CO2 will likely affect both the hydrologic cycle and ecosystem productivity. Current assumptions that increasing CO2 will lead to increased ecosystem productivity and plant water use efficiency (WUE) are driving optimistic predictions of higher crop yields as well as greater availability of freshwater resources due to a decrease in evapotranspiration. The plant physiological response that drives these effects is believed to be an increase in carbon uptake either by (a) stronger CO2 gradient between the stomata and the atmosphere, or by (b) reduced CO2 limitation of enzymatic carboxylation within the leaf. The (a) scenario will lead to increased water use efficiency (WUE) in plants. However, evidence for increased WUE is mostly based on modeling studies, and experiments producing a short duration or step-wise increase in CO2 concentration (e.g. free-air CO2 enrichment). We hypothesize that the increase in atmospheric CO2 concentration is having a positive effect on ecosystem productivity and WUE. To investigate this hypothesis, we analyzed meteorological, ANPP, and soil CO2 flux datasets together with carbon isotopic ratio (13C/12C) of archived plant samples from the long term ecological research (LTER) program at Kellogg Biological Station. The datasets were collected between 1989 and 2007 (corresponding to an increase in atmospheric CO2 concentration of ~33 ppmv at Mauna Loa). Wheat (Triticum aestivum) samples taken from 1989 and 2007 show a significant decrease in the C isotope discrimination factor (Δ) over time. Stomatal conductance is directly related to Δ, and thus Δ is inversely related to plant intrinsic WUE (iWUE). Historical changes in the 13C/12C ratio (δ13C) in samples of a perennial forb, Canada goldenrod (Solidago canadensis), taken from adjacent successional fields, indicate changes in Δ upon uptake of CO2 as well. These temporal trends in Δ suggest a positive feedback between the increasing CO2 concentration in the atmosphere, air temperature, and plant iWUE. This positive feedback is expressed by (a) nonparallel changes of δ13C signal of atmospheric CO2 (δa) and plant samples (δp), (b) negative correlation between the Δ and average temperatures during the growth season, although only for temperatures up to 21°C. The lack of effect at higher temperatures suggests a negative influence of growing season warming on the iWUE. These results suggest a complex feedback between atmospheric CO2 increase, plant physiology, ecosystem productivity, and soil CO2 fluxes. These complex effects support our hypothesis of a CO2 fertilization effect on plant productivity, and they raise additional questions regarding adaptation of plants to changing atmospheric CO2 and climate.

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

NASA Technical Reports Server (NTRS)

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

2010-01-01

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

Orbiting Carbon Observatory

NASA Technical Reports Server (NTRS)

Miller, Charles E.

2005-01-01

Human impact on the environment has produced measurable changes in the geological record since the late 1700s. Anthropogenic emissions of CO2 today may cause the global climate to depart for its natural behavior for many millenia. CO2 is the primary anthropogenic driver of climate change. The Orbiting Carbon Observatory goals are to help collect measurements of atmospheric CO2, answering questions such as why the atmospheric CO2 buildup varies annually, the roles of the oceans and land ecosystems in absorbing CO2, the roles of North American and Eurasian sinks and how these carbon sinks respond to climate change. The present carbon cycle, CO2 variability, and climate uncertainties due atmospheric CO2 uncertainties are highlighted in this presentation.

Moss and soil contributions to the annual net carbon flux of a maturing boreal forest

USGS Publications Warehouse

Harden, J.W.; O'Neill, K. P.; Trumbore, S.E.; Veldhuis, H.; Stocks, B.J.

1997-01-01

We used input and decomposition data from 14C studies of soils to determine rates of vertical accumulation of moss combined with carbon storage inventories on a sequence of burns to model how carbon accumulates in soils and moss after a stand-killing fire. We used soil drainage - moss associations and soil drainage maps of the old black spruce (OBS) site at the BOREAS northern study area (NSA) to areally weight the contributions of each moderately well drained, feathermoss areas; poorly drained sphagnum - feathermoss areas; and very poorly drained brown moss areas to the carbon storage and flux at the OBS NSA site. On this very old (117 years) complex of black spruce, sphagnum bog veneer, and fen systems we conclude that these systems are likely sequestering 0.01-0.03 kg C m-2 yr-' at OBS-NSA today. Soil drainage in boreal forests near Thompson, Manitoba, controls carbon storage and flux by controlling moss input and decomposition rates and by controlling through fire the amount and quality of carbon left after burning. On poorly drained soils rich in sphagnum moss, net accumulation and long-term storage of carbon is higher than on better drained soils colonized by feathermosses. The carbon flux of these contrasting ecosystems is best characterized by soil drainage class and stand age, where stands recently burned are net sources of CO2, and maturing stands become increasingly stronger sinks of atmospheric CO2. This approach to measuring carbon storage and flux presents a method of scaling to larger areas using soil drainage, moss cover, and stand age information.

Modeling soil carbon sequestration with EPIC and the soil conditioning index

USDA-ARS?s Scientific Manuscript database

Increasing CO2 in the atmosphere is a concern, because of its potential to warm the planet. CO2 and other greenhouse gases act as a barrier to prevent heat escaping from the atmosphere. Prior to the industrial revolution, atmospheric CO2 concentration was about 280 parts per million (ppm). A deli...

Sequestration of non-pure carbon dioxide streams in iron oxyhydroxide-containing saline repositories

USGS Publications Warehouse

Garcia, S.; Rosenbauer, Robert J.; Palandri, James L.; Maroto-Valer, M. Mercedes

2012-01-01

Iron oxyhydroxide, goethite (α-FeOOH), was evaluated as a potential formation mineral reactant for trapping CO2 in a mineral phase such as siderite (FeCO3), when a mixture of CO2-SO 2 flue gas is injected into a saline aquifer. Two thermodynamic simulations were conducted, equilibrating a CO2-SO2 fluid mixture with a NaCl-brine and Fe-rich rocks at 150 °C and 300 bar. The modeling studies evaluated mineral and fluid composition at equilibrium and the influence of pH buffering in the system. Results show siderite precipitates both in the buffered and unbuffered system; however, the presence of an alkaline pH buffer enhances the stability of the carbonate. Based on the model, an experiment was designed to compare with thermodynamic predictions. A CO2-SO2 gas mixture was reacted in 150 ml of NaCl-NaOH brine containing 10 g of goethite at 150 °C and 300 bar for 24 days. Mineralogical and brine chemistry confirmed siderite as the predominant reaction product in the system. Seventy-six mg of CO2 are sequestered in siderite per 10 g of goethite.

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

NASA Astrophysics Data System (ADS)

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

2015-04-01

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

Speleothems as proxy for the carbon isotope composition of atmospheric CO2

NASA Astrophysics Data System (ADS)

Baskaran, M.; Krishnamurthy, R. V.

1993-12-01

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

Influence of modified atmosphere packaging on the shelf life of prebaked pizza dough with and without preservative added.

PubMed

Rodríguez, Valle; Medina, Luis; Jordano, Rafael

2003-04-01

The possible effect of different modified atmospheres on the shelf life of prebaked pizza dough, with and without added calcium propionate, was investigated. Three packaging atmospheres were tested: 20% CO2: 80% N2, 50% CO2: 50% N2, 100% CO2, and air (control). Samples were examined daily for visible mold growth and analysed after 2, 8, 17 and 31 days throughout storage (15-20 degrees C and 54-65% relative humidity, RH) for changes in gaseous composition, pH and microbial populations (mesophilic aerobic and anaerobic bacteria, lactic acid bacteria (LAB), and yeasts and molds). Microbiological results showed that molds had a greater sensitivity to CO2 than bacteria and yeasts. Products containing calcium propionate did not show mold growth throughout storage (31 days) when packaged in air or in CO2-enriched atmospheres (20, 50 and 100%). However, in pizza dough without preservative (calcium propionate), mold growth was evident after 7 days, except under 100% CO2 atmosphere (13 days) regardless of the packaging atmosphere. From these results we conclude that the addition of calcium propionate had more and decisive influence on the shelf life extension of prebaked pizza dough.

Effect of increasing CO2 on the terrestrial carbon cycle

PubMed Central

Schimel, David; Fisher, Joshua B.

2015-01-01

Feedbacks from the terrestrial carbon cycle significantly affect future climate change. The CO2 concentration dependence of global terrestrial carbon storage is one of the largest and most uncertain feedbacks. Theory predicts the CO2 effect should have a tropical maximum, but a large terrestrial sink has been contradicted by analyses of atmospheric CO2 that do not show large tropical uptake. Our results, however, show significant tropical uptake and, combining tropical and extratropical fluxes, suggest that up to 60% of the present-day terrestrial sink is caused by increasing atmospheric CO2. This conclusion is consistent with a validated subset of atmospheric analyses, but uncertainty remains. Improved model diagnostics and new space-based observations can reduce the uncertainty of tropical and temperate zone carbon flux estimates. This analysis supports a significant feedback to future atmospheric CO2 concentrations from carbon uptake in terrestrial ecosystems caused by rising atmospheric CO2 concentrations. This feedback will have substantial tropical contributions, but the magnitude of future carbon uptake by tropical forests also depends on how they respond to climate change and requires their protection from deforestation. PMID:25548156

Mercury Adsorption and Oxidation over Cobalt Oxide Loaded Magnetospheres Catalyst from Fly Ash in Oxyfuel Combustion Flue Gas.

PubMed

Yang, Jianping; Zhao, Yongchun; Chang, Lin; Zhang, Junying; Zheng, Chuguang

2015-07-07

Cobalt oxide loaded magnetospheres catalyst from fly ash (Co-MF catalyst) showed good mercury removal capacity and recyclability under air combustion flue gas in our previous study. In this work, the Hg(0) removal behaviors as well as the involved reactions mechanism were investigated in oxyfuel combustion conditions. Further, the recyclability of Co-MF catalyst in oxyfuel combustion atmosphere was also evaluated. The results showed that the Hg(0) removal efficiency in oxyfuel combustion conditions was relative high compared to that in air combustion conditions. The presence of enriched CO2 (70%) in oxyfuel combustion atmosphere assisted the mercury oxidation due to the oxidation of function group of C-O formed from CO2. Under both atmospheres, the mercury removal efficiency decreased with the addition of SO2, NO, and H2O. However, the enriched CO2 in oxyfuel combustion atmosphere could somewhat weaken the inhibition of SO2, NO, and H2O. The multiple capture-regeneration cycles demonstrated that the Co-MF catalyst also present good regeneration performance in oxyfuel combustion atmosphere.

Simulation of reactive transport of injected CO2 on the Colorado Plateau, Utah, USA

USGS Publications Warehouse

White, S.P.; Allis, R.G.; Moore, J.; Chidsey, T.; Morgan, C.; Gwynn, W.; Adams, M.

2005-01-01

This paper investigates injection of CO2 into non-dome-shaped geological structures that do not provide the traps traditionally deemed necessary for the development of artificial CO2 reservoirs. We have developed a conceptual and two numerical models of the geology and groundwater along a cross-section lying approximately NW-SE and in the vicinity of the Hunter power station on the Colorado Plateau, Central Utah and identified a number of potential sequestration sites on this cross-section. Preliminary modeling identified the White Rim Sandstone as appearing to offer the properties required of a successful sequestration site. Detailed modeling of injection of CO2 into the White Rim Sandstone using the reactive chemical simulator ChemTOUGH found that 1000 years after the 30 year injection period began approximately 21% of the injected CO2 was permanently sequestered as a mineral, 52% was beneath the ground surface as a gas or dissolved in the groundwater and 17% had leaked to the surface and leakage to the surface was continuing. ?? 2005 Elsevier B.V. All rights reserved.

Atmospheric measurement of point source fossil CO2 emissions

NASA Astrophysics Data System (ADS)

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

2014-05-01

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

Atmospheric inversion of the surface CO2 flux with 13CO2 constraint

NASA Astrophysics Data System (ADS)

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

2013-10-01

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

Implications for carbon processing beneath the Greenland Ice Sheet from dissolved CO2 and CH4 concentrations of subglacial discharge

NASA Astrophysics Data System (ADS)

Pain, A.; Martin, J.; Martin, E. E.

2017-12-01

Subglacial carbon processes are of increasing interest as warming induces ice melting and increases fluxes of glacial meltwater into proglacial rivers and the coastal ocean. Meltwater may serve as an atmospheric source or sink of carbon dioxide (CO2) or methane (CH4), depending on the magnitudes of subglacial organic carbon (OC) remineralization, which produces CO2 and CH4, and mineral weathering reactions, which consume CO2 but not CH4. We report wide variability in dissolved CO2 and CH4 concentrations at the beginning of the melt season (May-June 2017) between three sites draining land-terminating glaciers of the Greenland Ice Sheet. Two sites, located along the Watson River in western Greenland, drain the Isunnguata and Russell Glaciers and contained 1060 and 400 ppm CO2, respectively. In-situ CO2 flux measurements indicated that the Isunnguata was a source of atmospheric CO2, while the Russell was a sink. Both sites had elevated CH4 concentrations, at 325 and 25 ppm CH4, respectively, suggesting active anaerobic OC remineralization beneath the ice sheet. Dissolved CO2 and CH4 reached atmospheric equilibrium within 2.6 and 8.6 km downstream of Isunnguata and Russell discharge sites, respectively. These changes reflect rapid gas exchange with the atmosphere and/or CO2 consumption via instream mineral weathering. The third site, draining the Kiagtut Sermiat in southern Greenland, had about half atmospheric CO2 concentrations (250 ppm), but approximately atmospheric CH4 concentrations (2.1 ppm). Downstream CO2 flux measurements indicated ingassing of CO2 over the entire 10-km length of the proglacial river. CO2 undersaturation may be due to more readily weathered lithologies underlying the Kiagtut Sermiat compared to Watson River sites, but low CH4 concentrations also suggest limited contributions of CO2 and CH4 from OC remineralization. These results suggest that carbon processing beneath the Greenland Ice Sheet may be more variable than previously recognized. Variations control whether discharge is a source or sink of atmospheric CO2 or CH4, but gas concentrations could be further modified by instream reactions. Increased meltwater fluxes should enhance the importance of greenhouse gas fluxes from subglacial discharge, and heighten the need to constrain variability in subglacial carbon processing.

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

NASA Astrophysics Data System (ADS)

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

2014-12-01

We have developed a novel framework ("Tan-Tracker") for assimilating observations of atmospheric CO2 concentrations, based on the POD-based (proper orthogonal decomposition) ensemble four-dimensional variational data assimilation method (PODEn4DVar). The high flexibility and the high computational efficiency of the PODEn4DVar approach allow us to include both the atmospheric CO2 concentrations and the surface CO2 fluxes as part of the large state vector to be simultaneously estimated from assimilation of atmospheric CO2 observations. Compared to most modern top-down flux inversion approaches, where only surface fluxes are considered as control variables, one major advantage of our joint data assimilation system is that, in principle, no assumption on perfect transport models is needed. In addition, the possibility for Tan-Tracker to use a complete dynamic model to consistently describe the time evolution of CO2 surface fluxes (CFs) and the atmospheric CO2 concentrations represents a better use of observation information for recycling the analyses at each assimilation step in order to improve the forecasts for the following assimilations. An experimental Tan-Tracker system has been built based on a complete augmented dynamical model, where (1) the surface atmosphere CO2 exchanges are prescribed by using a persistent forecasting model for the scaling factors of the first-guess net CO2 surface fluxes and (2) the atmospheric CO2 transport is simulated by using the GEOS-Chem three-dimensional global chemistry transport model. Observing system simulation experiments (OSSEs) for assimilating synthetic in situ observations of surface CO2 concentrations are carefully designed to evaluate the effectiveness of the Tan-Tracker system. In particular, detailed comparisons are made with its simplified version (referred to as TT-S) with only CFs taken as the prognostic variables. It is found that our Tan-Tracker system is capable of outperforming TT-S with higher assimilation precision for both CO2 concentrations and CO2 fluxes, mainly due to the simultaneous estimation of CO2 concentrations and CFs in our Tan-Tracker data assimilation system. A experiment for assimilating the real dry-air column CO2 retrievals (XCO2) from the Japanese Greenhouse Gases Observation Satellite (GOSAT) further demonstrates its potential wide applications.

Calcium silicates synthesised from industrial residues with the ability for CO2 sequestration.

PubMed

Morales-Flórez, Victor; Santos, Alberto; López, Antonio; Moriña, Isabel; Esquivias, Luis

2014-12-01

This work explored several synthesis routes to obtain calcium silicates from different calcium-rich and silica-rich industrial residues. Larnite, wollastonite and calcium silicate chloride were successfully synthesised with moderate heat treatments below standard temperatures. These procedures help to not only conserve natural resources, but also to reduce the energy requirements and CO2 emissions. In addition, these silicates have been successfully tested as carbon dioxide sequesters, to enhance the viability of CO2 mineral sequestration technologies using calcium-rich industrial by-products as sequestration agents. Two different carbon sequestration experiments were performed under ambient conditions. Static experiments revealed carbonation efficiencies close to 100% and real-time resolved experiments characterised the dynamic behaviour and ability of these samples to reduce the CO2 concentration within a mixture of gases. The CO2 concentration was reduced up to 70%, with a carbon fixation dynamic ratio of 3.2 mg CO2 per g of sequestration agent and minute. Our results confirm the suitability of the proposed synthesis routes to synthesise different calcium silicates recycling industrial residues, being therefore energetically more efficient and environmentally friendly procedures for the cement industry. © The Author(s) 2014.

Independent evaluation of point source fossil fuel CO2 emissions to better than 10%

PubMed Central

Turnbull, Jocelyn Christine; Keller, Elizabeth D.; Norris, Margaret W.; Wiltshire, Rachael M.

2016-01-01

Independent estimates of fossil fuel CO2 (CO2ff) emissions are key to ensuring that emission reductions and regulations are effective and provide needed transparency and trust. Point source emissions are a key target because a small number of power plants represent a large portion of total global emissions. Currently, emission rates are known only from self-reported data. Atmospheric observations have the potential to meet the need for independent evaluation, but useful results from this method have been elusive, due to challenges in distinguishing CO2ff emissions from the large and varying CO2 background and in relating atmospheric observations to emission flux rates with high accuracy. Here we use time-integrated observations of the radiocarbon content of CO2 (14CO2) to quantify the recently added CO2ff mole fraction at surface sites surrounding a point source. We demonstrate that both fast-growing plant material (grass) and CO2 collected by absorption into sodium hydroxide solution provide excellent time-integrated records of atmospheric 14CO2. These time-integrated samples allow us to evaluate emissions over a period of days to weeks with only a modest number of measurements. Applying the same time integration in an atmospheric transport model eliminates the need to resolve highly variable short-term turbulence. Together these techniques allow us to independently evaluate point source CO2ff emission rates from atmospheric observations with uncertainties of better than 10%. This uncertainty represents an improvement by a factor of 2 over current bottom-up inventory estimates and previous atmospheric observation estimates and allows reliable independent evaluation of emissions. PMID:27573818

Independent evaluation of point source fossil fuel CO2 emissions to better than 10%.

PubMed

Turnbull, Jocelyn Christine; Keller, Elizabeth D; Norris, Margaret W; Wiltshire, Rachael M

2016-09-13

Independent estimates of fossil fuel CO2 (CO2ff) emissions are key to ensuring that emission reductions and regulations are effective and provide needed transparency and trust. Point source emissions are a key target because a small number of power plants represent a large portion of total global emissions. Currently, emission rates are known only from self-reported data. Atmospheric observations have the potential to meet the need for independent evaluation, but useful results from this method have been elusive, due to challenges in distinguishing CO2ff emissions from the large and varying CO2 background and in relating atmospheric observations to emission flux rates with high accuracy. Here we use time-integrated observations of the radiocarbon content of CO2 ((14)CO2) to quantify the recently added CO2ff mole fraction at surface sites surrounding a point source. We demonstrate that both fast-growing plant material (grass) and CO2 collected by absorption into sodium hydroxide solution provide excellent time-integrated records of atmospheric (14)CO2 These time-integrated samples allow us to evaluate emissions over a period of days to weeks with only a modest number of measurements. Applying the same time integration in an atmospheric transport model eliminates the need to resolve highly variable short-term turbulence. Together these techniques allow us to independently evaluate point source CO2ff emission rates from atmospheric observations with uncertainties of better than 10%. This uncertainty represents an improvement by a factor of 2 over current bottom-up inventory estimates and previous atmospheric observation estimates and allows reliable independent evaluation of emissions.

Using radiocarbon to investigate soil respiration impacts on atmospheric CO2

NASA Astrophysics Data System (ADS)

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

2013-12-01

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

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

PubMed

Moreira, Diana; Pires, José C M

2016-09-01

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

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

NASA Astrophysics Data System (ADS)

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

2016-04-01

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

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

PubMed

Fleischer, Siegfried

2003-02-01

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

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

NASA Astrophysics Data System (ADS)

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

2009-04-01

Nowadays one of the most burning questions for the science is the rate and the reasons of the recent climate change. Greenhouse gases (GHG), mainly CO2 and CH4 in the atmosphere could affect the climate of our planet. However, the relation between the amount of atmospheric GHG and the climate is complex, full with interactions and feedbacks partly poorly known even by now. The only way to understand the processes, to trace the changes, to develop and validate mathematical models for forecasts is the extensive, high precision, continuous monitoring of the atmosphere. Fossil fuel CO2 emissions are a major component of the European carbon budget. Separation of the fossil fuel signal from the natural biogenic one in the atmosphere is, therefore, a crucial task for quantifying exchange flux of the continental biosphere through atmospheric observations and inverse modelling. An independent method to estimate trace gas emissions is the top-down approach, using atmospheric CO2 concentration measurements combined with simultaneous radiocarbon (14C) observations. As adding fossil fuel CO2 to the atmosphere, therefore, leads not only to an increase in the CO2 content of the atmosphere but also to a decrease in the 14C/12C ratio in atmospheric CO2. The ATOMKI has more than two decade long experience in atmospheric 14CO2 monitoring. As a part of an ongoing research project being carried out in Hungary to investigate the amount and temporal and spatial variations of fossil fuel CO2 in the near surface atmosphere we developed a mobile and high-precision atmospheric CO2 monitoring station. We describe the layout and the operation of the measuring system which is designed for the continuous, unattended monitoring of CO2 mixing ratio in the near surface atmosphere based on an Ultramat 6F (Siemens) infrared gas analyser. In the station one atmospheric 14CO2 sampling unit is also installed which is developed and widely used since more than one decade by ATOMKI. Mixing ratio of CO2 is measured at 2 m above the ground by the monitoring station. Air is pumped through a 9.5-mm-diameter plastic tube (PFA, Swagelok) to a CO2 analyser located in a container box. Container box (Containex) is 1.5 m wide, 1.2 m deep and 2.2 m high, designed as a mobile measuring room which is field deployable, only electric power is required. A 15 micron pore size stainless steel Tee-Type (Swagelok) particle filter is located at the inlet of the sampler tube. Diaphragm pump (KNF) is used to draw air continuously through the sampling tube from monitoring level at flow rate of ~ 2 L/min. After leaving the pump, the air at 5 psig overpressure enters a glass trap for liquid water that is cooled in a regular household refrigerator, to dry the air to a dew point of 3°-4°C. Liquid water is forced out through an orifice at the bottom of the trap. The air sample inlet tube and the standard gases (Linde Hungary) are connected to miniature solenoid valves (S Series, ASCO Numatics) in a manifold which are normally closed and controlled by the CO2 analyser, which selects which gas is sampled. The air leaving the manifold through its common outlet is further dried to a dew point of about -25°C by passage through a 360-cm-long Nafion drier (Permapure), so that the water vapour interference and dilution effect are <0.1 ppm equivalent CO2. The Nafion drier is purged in a counter flow (300 cm3/min) arrangement using waste sample air that has been further dried by passage through anhydrous CaSO4 (Drierite). Analysis is carried out using an infrared gas analyser Ultramat 6F which is a specialised model for field applications by Siemens. A constant sample flow rate of 300 cm3/min is maintained by a mass flow controller (Aalborg). The reference cell of the CO2 analyzer is continuously flushed with a compressed reference gas of 350 ppm CO2 in synthetic air (Messer Hungarogáz). The basic calibration cycle is 2 hours, consisting of a zero-point calibration and a span calibration. Each calibration is consisting of 2 min flushing and 20 sec signal integration. The usual change of the response function is below 0.2 ppm after 2 hours following a previous calibration. The analyser measures the CO2 mixing ratio in the sample gas in every 3 seconds. Output data are registered by a data logger developed for this application (Special Control Devices). The overall uncertainty of our atmospheric CO2 mixing ratio measurements is < 0.5 ppm (< 0,2 %). This level of error is acceptable for fossil fuel CO2 calculations as the uncertainty of the other required parameter radiocarbon content of atmospheric CO2 is usually 0.3-0.5%. Using the developed mobile and high-precision atmospheric CO2 monitoring station we plan to determine the fossil fuel CO2 amount in the air of different cities and other average industrial regions in Hungary. This research project was supported by Hungarian NSF (Ref No. F69029).

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

NASA Technical Reports Server (NTRS)

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

2015-01-01

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

Orbiting carbon observatory (OCO-2) tracks increase of carbon release to the atmosphere during the 2014-2016 El Niño

NASA Astrophysics Data System (ADS)

Patra, P. K.; Crisp, D.; W Kaiser, J.; Wunch, D.; Saeki, T.; Ichii, K.; Sekiya, T.; Wenneberg, P.; Griffith, D. W. T.; Feist, D. G.; Pollard, D.; Velazco, V. A.; De Maziere, M.; Sha, M. K.; Roehl, C. M.; Chatterjee, A.

2016-12-01

Uncertainties in estimates of regional fluxes of carbon dioxide (CO2) and other greenhouse gases derived from direct inventory methods or inferred from atmospheric observations has hindered the implementation of effective policy for reduction of emissions from anthropogenic activity. To improve the resolution and coverage of the atmospheric CO2 measurements for reducing CO2 flux uncertainty, NASA launched the OCO-2 satellite in 2014, and OCO-2 has been routinely returning almost one million soundings each day over the sunlit hemisphere. A powerful El Niño event in 2015-2016 - the third most intense since the 1950s - has exerted a large impact on the Earth's natural climate system. Here, we analyze column-averaged CO2 dry-air mole fraction (XCO2) observations during the period from September 2014 to February 2016 (18 months) together with ground-based remote sensing and in situ observations. From the differences between observations and simulations from an atmospheric chemistry-transport model, we estimated, that relative to the mean annual fluxes for 2011-2013, this El Niño has contributed to an excess CO2 flux from the Earth's surface (land+ocean) to the atmosphere in the range of 2.24-3.32 PgC (1 Pg = 1015 g). This anomalous CO2 flux results primarily from reduction in vegetation uptake due to drought and biomass burning. Improvements in modeling atmospheric-CO2 are required to attribute CO2 source changes at regional scales.

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

NASA Astrophysics Data System (ADS)

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

2013-12-01

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

Eastern equatorial pacific productivity and related-CO2 changes since the last glacial period.

PubMed

Calvo, Eva; Pelejero, Carles; Pena, Leopoldo D; Cacho, Isabel; Logan, Graham A

2011-04-05

Understanding oceanic processes, both physical and biological, that control atmospheric CO(2) is vital for predicting their influence during the past and into the future. The Eastern Equatorial Pacific (EEP) is thought to have exerted a strong control over glacial/interglacial CO(2) variations through its link to circulation and nutrient-related changes in the Southern Ocean, the primary region of the world oceans where CO(2)-enriched deep water is upwelled to the surface ocean and comes into contact with the atmosphere. Here we present a multiproxy record of surface ocean productivity, dust inputs, and thermocline conditions for the EEP over the last 40,000 y. This allows us to detect changes in phytoplankton productivity and composition associated with increases in equatorial upwelling intensity and influence of Si-rich waters of sub-Antarctic origin. Our evidence indicates that diatoms outcompeted coccolithophores at times when the influence of Si-rich Southern Ocean intermediate waters was greatest. This shift from calcareous to noncalcareous phytoplankton would cause a lowering in atmospheric CO(2) through a reduced carbonate pump, as hypothesized by the Silicic Acid Leakage Hypothesis. However, this change does not seem to have been crucial in controlling atmospheric CO(2), as it took place during the deglaciation, when atmospheric CO(2) concentrations had already started to rise. Instead, the concomitant intensification of Antarctic upwelling brought large quantities of deep CO(2)-rich waters to the ocean surface. This process very likely dominated any biologically mediated CO(2) sequestration and probably accounts for most of the deglacial rise in atmospheric CO(2).

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

NASA Astrophysics Data System (ADS)

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

2009-12-01

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

Nitrogen deposition and forest carbon sequestration: a quantitative synthesis from plot to global scales

NASA Astrophysics Data System (ADS)

Goodale, C. L.; Thomas, R. Q.; Dentener, F. J.; Adams, M.; Baron, J.; Emmett, B.; Evans, C. B.; Fernandez, I. J.; Gundersen, P.; Hagedorn, F.; Kulmatiski, A.; Lovett, G. M.; McNulty, S.; Melvin, A. M.; Moldan, F.; Ollinger, S. V.; Schleppi, P.; Weiss, M.

2009-12-01

Atmospheric nitrogen deposition has long been proposed as a driver of terrestrial carbon sequestration, but its quantitative effect remains poorly constrained. Global models, observations along N deposition gradients, and plot-level forest N-addition experiments provide a range of estimates of the amount of C sequestered in response to added N. Synthesis of results from 48 multi-year N-addition studies in temperate forests show responses ranging from +53 to -95 kg C of live tree production per unit of N addition. Negative effects on live tree C occurred in stands with low rates of biomass accumulation, and occurred more rapidly with higher N application rates. More positive effects occurred in younger stands, and with greater efficiency of C gain at lower N addition rates. Observations of tree growth along N deposition gradients in Europe and the eastern U.S. produced broadly similar tree growth responses (19-56 kg C/kg N) as the N addition experiments. Soil C response increased with N addition rate, and averaged 4 + 12 kg C/kg N. These surface soil responses suggest modest suppression of soil decomposition induced by added N in some but not all sites due to several possible mechanisms, none of which are yet considered in global models. Global-scale estimates of N deposition effects on forest C sequestration have ranged from 0.1 to 2.0 Pg C/y depending on assumptions on the rate of N deposition to forests, its fate, and the C:N ratios of recipient C pools. A new group of biogeochemistry models designed for coupling with global climate models all simulate relatively limited terrestrial C sinks from atmospheric N deposition alone (0.2 - 0.4 PgC/y), more in combination with rising atmospheric CO2. Future model projections should benefit from rigorous comparisons with the range of observed C responses reviewed here.

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

NASA Technical Reports Server (NTRS)

Zent, A. P.

1992-01-01

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

The interaction of climate change and methane hydrates

USGS Publications Warehouse

Ruppel, Carolyn D.; Kessler, John D.

2017-01-01

Gas hydrate, a frozen, naturally-occurring, and highly-concentrated form of methane, sequesters significant carbon in the global system and is stable only over a range of low-temperature and moderate-pressure conditions. Gas hydrate is widespread in the sediments of marine continental margins and permafrost areas, locations where ocean and atmospheric warming may perturb the hydrate stability field and lead to release of the sequestered methane into the overlying sediments and soils. Methane and methane-derived carbon that escape from sediments and soils and reach the atmosphere could exacerbate greenhouse warming. The synergy between warming climate and gas hydrate dissociation feeds a popular perception that global warming could drive catastrophic methane releases from the contemporary gas hydrate reservoir. Appropriate evaluation of the two sides of the climate-methane hydrate synergy requires assessing direct and indirect observational data related to gas hydrate dissociation phenomena and numerical models that track the interaction of gas hydrates/methane with the ocean and/or atmosphere. Methane hydrate is likely undergoing dissociation now on global upper continental slopes and on continental shelves that ring the Arctic Ocean. Many factors—the depth of the gas hydrates in sediments, strong sediment and water column sinks, and the inability of bubbles emitted at the seafloor to deliver methane to the sea-air interface in most cases—mitigate the impact of gas hydrate dissociation on atmospheric greenhouse gas concentrations though. There is no conclusive proof that hydrate-derived methane is reaching the atmosphere now, but more observational data and improved numerical models will better characterize the climate-hydrate synergy in the future.

The interaction of climate change and methane hydrates

NASA Astrophysics Data System (ADS)

Ruppel, Carolyn D.; Kessler, John D.

2017-03-01

Gas hydrate, a frozen, naturally-occurring, and highly-concentrated form of methane, sequesters significant carbon in the global system and is stable only over a range of low-temperature and moderate-pressure conditions. Gas hydrate is widespread in the sediments of marine continental margins and permafrost areas, locations where ocean and atmospheric warming may perturb the hydrate stability field and lead to release of the sequestered methane into the overlying sediments and soils. Methane and methane-derived carbon that escape from sediments and soils and reach the atmosphere could exacerbate greenhouse warming. The synergy between warming climate and gas hydrate dissociation feeds a popular perception that global warming could drive catastrophic methane releases from the contemporary gas hydrate reservoir. Appropriate evaluation of the two sides of the climate-methane hydrate synergy requires assessing direct and indirect observational data related to gas hydrate dissociation phenomena and numerical models that track the interaction of gas hydrates/methane with the ocean and/or atmosphere. Methane hydrate is likely undergoing dissociation now on global upper continental slopes and on continental shelves that ring the Arctic Ocean. Many factors—the depth of the gas hydrates in sediments, strong sediment and water column sinks, and the inability of bubbles emitted at the seafloor to deliver methane to the sea-air interface in most cases—mitigate the impact of gas hydrate dissociation on atmospheric greenhouse gas concentrations though. There is no conclusive proof that hydrate-derived methane is reaching the atmosphere now, but more observational data and improved numerical models will better characterize the climate-hydrate synergy in the future.

The interaction of climate change and methane hydrates

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

Ruppel, Carolyn D.; Kessler, John D.

Gas hydrate, a frozen, naturally-occurring, and highly-concentrated form of methane, sequesters significant carbon in the global system and is stable only over a range of low-temperature and moderate-pressure conditions. Gas hydrate is widespread in the sediments of marine continental margins and permafrost areas, locations where ocean and atmospheric warming may perturb the hydrate stability field and lead to release of the sequestered methane into the overlying sediments and soils. Methane and methane-derived carbon that escape from sediments and soils and reach the atmosphere could exacerbate greenhouse warming. The synergy between warming climate and gas hydrate dissociation feeds a popular perceptionmore » that global warming could drive catastrophic methane releases from the contemporary gas hydrate reservoir. Appropriate evaluation of the two sides of the climate-methane hydrate synergy requires assessing direct and indirect observational data related to gas hydrate dissociation phenomena and numerical models that track the interaction of gas hydrates/methane with the ocean and/or atmosphere. Methane hydrate is likely undergoing dissociation now on global upper continental slopes and on continental shelves that ring the Arctic Ocean. Many factors—the depth of the gas hydrates in sediments, strong sediment and water column sinks, and the inability of bubbles emitted at the seafloor to deliver methane to the sea-air interface in most cases—mitigate the impact of gas hydrate dissociation on atmospheric greenhouse gas concentrations though. There is no conclusive proof that hydrate-derived methane is reaching the atmosphere now, but more observational data and improved numerical models will better characterize the climate-hydrate synergy in the future.« less

The interaction of climate change and methane hydrates

DOE PAGES

Ruppel, Carolyn D.; Kessler, John D.

2016-12-14

Gas hydrate, a frozen, naturally-occurring, and highly-concentrated form of methane, sequesters significant carbon in the global system and is stable only over a range of low-temperature and moderate-pressure conditions. Gas hydrate is widespread in the sediments of marine continental margins and permafrost areas, locations where ocean and atmospheric warming may perturb the hydrate stability field and lead to release of the sequestered methane into the overlying sediments and soils. Methane and methane-derived carbon that escape from sediments and soils and reach the atmosphere could exacerbate greenhouse warming. The synergy between warming climate and gas hydrate dissociation feeds a popular perceptionmore » that global warming could drive catastrophic methane releases from the contemporary gas hydrate reservoir. Appropriate evaluation of the two sides of the climate-methane hydrate synergy requires assessing direct and indirect observational data related to gas hydrate dissociation phenomena and numerical models that track the interaction of gas hydrates/methane with the ocean and/or atmosphere. Methane hydrate is likely undergoing dissociation now on global upper continental slopes and on continental shelves that ring the Arctic Ocean. Many factors—the depth of the gas hydrates in sediments, strong sediment and water column sinks, and the inability of bubbles emitted at the seafloor to deliver methane to the sea-air interface in most cases—mitigate the impact of gas hydrate dissociation on atmospheric greenhouse gas concentrations though. There is no conclusive proof that hydrate-derived methane is reaching the atmosphere now, but more observational data and improved numerical models will better characterize the climate-hydrate synergy in the future.« less

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

DOE PAGES

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

2016-07-22

Megacities are major sources of anthropogenic fossil fuel CO 2 (FFCO 2) emissions. The spatial extents of these large urban systems cover areas of 10 000 km 2 or more with complex topography and changing landscapes. We present a high-resolution land–atmosphere modelling system for urban CO 2 emissions over the Los Angeles (LA) megacity area. The Weather Research and Forecasting (WRF)-Chem model was coupled to a very high-resolution FFCO 2 emission product, Hestia-LA, to simulate atmospheric CO 2 concentrations across the LA megacity at spatial resolutions as fine as ~1 km. We evaluated multiple WRF configurations, selecting one that minimizedmore » errors in wind speed, wind direction, and boundary layer height as evaluated by its performance against meteorological data collected during the CalNex-LA campaign (May–June 2010). Our results show no significant difference between moderate-resolution (4 km) and high-resolution (1.3 km) simulations when evaluated against surface meteorological data, but the high-resolution configurations better resolved planetary boundary layer heights and vertical gradients in the horizontal mean winds. We coupled our WRF configuration with the Vulcan 2.2 (10 km resolution) and Hestia-LA (1.3 km resolution) fossil fuel CO 2 emission products to evaluate the impact of the spatial resolution of the CO 2 emission products and the meteorological transport model on the representation of spatiotemporal variability in simulated atmospheric CO 2 concentrations. We find that high spatial resolution in the fossil fuel CO 2 emissions is more important than in the atmospheric model to capture CO 2 concentration variability across the LA megacity. Finally, we present a novel approach that employs simultaneous correlations of the simulated atmospheric CO 2 fields to qualitatively evaluate the greenhouse gas measurement network over the LA megacity. Spatial correlations in the atmospheric CO 2 fields reflect the coverage of individual measurement sites when a statistically significant number of sites observe emissions from a specific source or location. We conclude that elevated atmospheric CO 2 concentrations over the LA megacity are composed of multiple fine-scale plumes rather than a single homogenous urban dome. Furthermore, we conclude that FFCO 2 emissions monitoring in the LA megacity requires FFCO 2 emissions modelling with ~1 km resolution because coarser-resolution emissions modelling tends to overestimate the observational constraints on the emissions estimates.« less

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

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

Feng, Sha; Lauvaux, Thomas; Newman, Sally

Megacities are major sources of anthropogenic fossil fuel CO 2 (FFCO 2) emissions. The spatial extents of these large urban systems cover areas of 10 000 km 2 or more with complex topography and changing landscapes. We present a high-resolution land–atmosphere modelling system for urban CO 2 emissions over the Los Angeles (LA) megacity area. The Weather Research and Forecasting (WRF)-Chem model was coupled to a very high-resolution FFCO 2 emission product, Hestia-LA, to simulate atmospheric CO 2 concentrations across the LA megacity at spatial resolutions as fine as ~1 km. We evaluated multiple WRF configurations, selecting one that minimizedmore » errors in wind speed, wind direction, and boundary layer height as evaluated by its performance against meteorological data collected during the CalNex-LA campaign (May–June 2010). Our results show no significant difference between moderate-resolution (4 km) and high-resolution (1.3 km) simulations when evaluated against surface meteorological data, but the high-resolution configurations better resolved planetary boundary layer heights and vertical gradients in the horizontal mean winds. We coupled our WRF configuration with the Vulcan 2.2 (10 km resolution) and Hestia-LA (1.3 km resolution) fossil fuel CO 2 emission products to evaluate the impact of the spatial resolution of the CO 2 emission products and the meteorological transport model on the representation of spatiotemporal variability in simulated atmospheric CO 2 concentrations. We find that high spatial resolution in the fossil fuel CO 2 emissions is more important than in the atmospheric model to capture CO 2 concentration variability across the LA megacity. Finally, we present a novel approach that employs simultaneous correlations of the simulated atmospheric CO 2 fields to qualitatively evaluate the greenhouse gas measurement network over the LA megacity. Spatial correlations in the atmospheric CO 2 fields reflect the coverage of individual measurement sites when a statistically significant number of sites observe emissions from a specific source or location. We conclude that elevated atmospheric CO 2 concentrations over the LA megacity are composed of multiple fine-scale plumes rather than a single homogenous urban dome. Furthermore, we conclude that FFCO 2 emissions monitoring in the LA megacity requires FFCO 2 emissions modelling with ~1 km resolution because coarser-resolution emissions modelling tends to overestimate the observational constraints on the emissions estimates.« less

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

NASA Technical Reports Server (NTRS)

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

1993-01-01

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

Comparing ecosystem and soil respiration: Review and key challenges of tower-based and soil mesurements

USDA-ARS?s Scientific Manuscript database

The net ecosystem exchange (NEE) is the difference between ecosystem CO2 assimilation and CO2 losses to the atmosphere. Ecosystem respiration (Reco), the efflux of CO2 from the ecosystem to the atmosphere, includes the soil-to-atmosphere carbon flux (i.e., soil respiration; Rsoil) and aboveground pl...

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

Treesearch

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

2013-01-01

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

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

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

Gao, Peter; Hu, Renyu; Li, Cheng

2015-06-20

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

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

NASA Technical Reports Server (NTRS)

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

The 2015-2016 El Nino and the Response of the Carbon Cycle: Findings from NASA's OCO-2 Mission

NASA Technical Reports Server (NTRS)

Chatterjee, Abhishek; Schimel, D.; Stephens, B.; Crisp, D.; Eldering, A.; Feely, R.; Gierach, M.; Gunson, M.; Keeling, R.; Landschuetzer, P.;

Long-term results from an urban CO2 monitoring network

NASA Astrophysics Data System (ADS)

Ehleringer, J.; Pataki, D. E.; Lai, C.; Schauer, A.

2009-12-01

High-precision atmospheric CO2 has been monitored in several locations through the Salt Lake Valley metropolitan region of northern Utah over the past nine years. Many parts of this semi-arid grassland have transitioned into dense urban forests, supported totally by extensive homeowner irrigation practices. Diurnal changes in fossil-fuel energy uses and photosynthesis-respiration processes have resulted in significant spatial and temporal variations in atmospheric CO2. Here we present an analysis of the long-term patterns and trends in midday and nighttime CO2 values for four sites: a midvalley residential neighborhood, a midvalley non-residential neighborhood, an undeveloped valley-edge area transitioning from agriculture, and a developed valley-edge neighborhood with mixed residential and commercial activities; the neighborhoods span an elevation gradient within the valley of ~100 m. Patterns in CO2 concentrations among neighborhoods were examined relative to each other and relative to the NOAA background station, a desert site in Wendover, Utah. Four specific analyses are considered. First, we present a statistical analysis of weekday versus weekend CO2 patterns in the winter, spring, summer, and fall seasons. Second, we present a statistical analysis of the influences of high-pressure systems on the elevation of atmospheric CO2 above background levels in the winter versus summer seasons. Third, we present an analysis of the nighttime CO2 values through the year, relating these patterns to observed changes in the carbon isotope ratios of atmospheric CO2. Lastly, we examine the rate of increase in midday urban CO2 over time relative to regional and global CO2 averages to determine if the amplification of urban energy use is statistically detectable from atmospheric trace gas measurements over the past decade. These results show two important patterns. First, there is a strong weekday-weekend effect of vehicle emissions in contrast to the temperature-dependent effect of home-heating emissions on diurnal/seasonal cycles. Second, there appears to be photosynthetic drawdown of atmospheric CO2 levels during the growing season, but at a cost of significant water expenditure. To the degree that atmospheric CO2 and particulate matter levels are correlated, these results have implications for both climate and health issues.

Carbonate system parameters and anthropogenic CO2 in the North Aegean Sea during October 2013

NASA Astrophysics Data System (ADS)

Krasakopoulou, E.; Souvermezoglou, E.; Giannoudi, L.; Goyet, C.

2017-10-01

Data of AT (total alkalinity) and CT (total inorganic carbon) collected during October 2013, on a N-S transect crossing the North of Lemnos basin allowed to identify the peculiarities of the CO2 system in the North Aegean Sea and estimate the anthropogenic CO2 (CANT) concentrations. Extremely high concentrations of AT and CT were recorded in the upper layer of the North Aegean reflecting the high loads of AT and CT by the brackish BSW (Black Sea Water) outflowing through the Dardanelles strait and by the rivers runoff. Both AT and CT exhibit strong negative linear correlation with salinity in the upper layer (0-20 m). Investigation of the AT-S relationship along with the salinity adjustment of AT revealed excess alkalinity throughout the water column in relation to the surface waters implying a possible occurrence of non-carbonate alkalinity inputs as well as of other processes that take place probably over the extended shelves and contribute to the alkalinity surplus. The intermediate layer occupied by the Modified Levantine Intermediate Water (MLIW) mass exhibits the lowest CT and AT concentrations, while rather elevated AT and CT concentrations characterize the North Aegean Deep Water (NAgDW) mass filling the deep layer of the North of Lemnos basin linked to previous dense water formation episodes. High anthropogenic CO2 content was detected at intermediate and deep layers of the North Aegean reflecting the effective transportation of the absorbed atmospheric CO2 from the surface to the deeper waters via the dense water formation episodes. The MLIW layer is more affected by the penetration of CANT than the NAgDW that fills the deep part of the basin. The observed variability of CANT distribution reflects the influence of the intensity of dense water formation events, of the different θ/S properties of the newly formed dense waters as well as of the diverse submarine pathways followed by the cascading dense waters. The invasion of CANT has lead to more acidic conditions and to lower saturation degree of calcium carbonate in relation to the preindustrial era. The findings of this study provide baseline information about the carbonate system properties of the North Aegean and highlight its active role in sequestering and storing anthropogenic CO2.

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

NASA Astrophysics Data System (ADS)

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

2017-12-01

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

The Fate and Stability of Eroding Wetland Soil Carbon in a Subsiding Deltaic Coastal Plain

NASA Astrophysics Data System (ADS)

White, J. R.; Steinmuller, H.; Chambers, L. G.; Fontenot, A.

2017-12-01

Coastal wetlands can respond to rapid rates of relative sea level rise via wetland submergence and/or erosion, which occur when wetlands are unable to vertically accrete to keep pace with sea level rise. As coastal wetlands erode, previously sequestered organic carbon is exposed to oxygen-rich estuarine water. This transition in redox from anaerobic to aerobic condition can trigger increased mineralization rates of decades to centuries'-old soil carbon. Barataria Bay, Louisiana has one of the highest coastal wetland land loss rates in the United States, primarily due to eustatic sea level rise coupled with coastal subsidence. Marsh-edge erosion rates measured over the past two years are on the order of 1.5 meters per year. Meter long soil cores were obtained from vegetated wetland sites and sectioned into 11 intervals to investigate aerobic and anaerobic mineralization rates with depth. In surface soils, organic carbon mineralization rates averaged 16 times greater than anaerobic mineralization rates. In deeper, older soils, the aerobic mineralization rate was still an order of magnitude greater than the anaerobic rate, suggesting a significant portion of this older, soil carbon is readily cycling back to the atmosphere after erosion followed by mineralization by microorganisms. These results have consequences for increased atmospheric CO2 concentrations in the future, as stable coastlines worldwide will be subjected to Barataria-bay levels of sea level rise in the next 50-75 years.

Preliminary work of mangrove ecosystem carbon stock mapping in small island using remote sensing: above and below ground carbon stock mapping on medium resolution satellite image

NASA Astrophysics Data System (ADS)

Wicaksono, Pramaditya; Danoedoro, Projo; Hartono, Hartono; Nehren, Udo; Ribbe, Lars

2011-11-01

Mangrove forest is an important ecosystem located in coastal area that provides various important ecological and economical services. One of the services provided by mangrove forest is the ability to act as carbon sink by sequestering CO2 from atmosphere through photosynthesis and carbon burial on the sediment. The carbon buried on mangrove sediment may persist for millennia before return to the atmosphere, and thus act as an effective long-term carbon sink. Therefore, it is important to understand the distribution of carbon stored within mangrove forest in a spatial and temporal context. In this paper, an effort to map carbon stocks in mangrove forest is presented using remote sensing technology to overcome the handicap encountered by field survey. In mangrove carbon stock mapping, the use of medium spatial resolution Landsat 7 ETM+ is emphasized. Landsat 7 ETM+ images are relatively cheap, widely available and have large area coverage, and thus provide a cost and time effective way of mapping mangrove carbon stocks. Using field data, two image processing techniques namely Vegetation Index and Linear Spectral Unmixing (LSU) were evaluated to find the best method to explain the variation in mangrove carbon stocks using remote sensing data. In addition, we also tried to estimate mangrove carbon sequestration rate via multitemporal analysis. Finally, the technique which produces significantly better result was used to produce a map of mangrove forest carbon stocks, which is spatially extensive and temporally repetitive.

Electrical Resistance Tomography Field Trials to Image CO2 Sequestration

NASA Astrophysics Data System (ADS)

Newmark, R.

2003-12-01

If geologic formations are used to sequester or store carbon dioxide (CO2) for long periods of time, it will be necessary to verify the containment of injected CO2 by assessing leaks and flow paths, and by understanding the geophysical and geochemical interactions between the CO2 and the geologic minerals and fluids. Remote monitoring methods are preferred, to minimize cost and impact to the integrity of the disposal reservoir. Electrical methods are especially well suited for monitoring processes involving fluids, as electrical properties are most sensitive to the presence and nature of the fluids contained in the medium. High resolution tomographs of electrical properties have been used with success for site characterization, monitoring subsurface migration of fluids in instances of leaking underground tanks, water infiltration events, subsurface steam floods, contaminant movement, and assessing the integrity of subsurface barriers. These surveys are commonly conducted utilizing vertical arrays of point electrodes in a crosswell configuration. Alternative ways of monitoring the reservoir are desirable due to the high costs of drilling the required monitoring boreholes Recent field results obtained using steel well casings as long electrodes are also promising. We have conducted field trials to evaluate the effectiveness of long electrode ERT as a potential monitoring approach for CO2 sequestration. In these trials, CO2 is not being sequestered but rather is being used as a solvent for enhanced oil recovery. This setting offers the same conditions expected during sequestration so monitoring secondary oil recovery allows a test of the method under realistic physical conditions and operational constraints. Field experience has confirmed the challenges identified during model studies. The principal difficulty are the very small signals due to the fact that formation changes occur only over a small segment of the 5000 foot length of the electrodes. In addition, telluric noise can be comparable to the signal levels during periods of geomagnetic activity. Finally, instrumentation stability over long periods is necessary to follow trends in reservoir behavior for several years. Solutions to these and other problems will be presented along with results from the first two years of work at a producing field undergoing CO2 flood. If electrical resistance tomography (ERT) imaging can be performed using existing well casings as long electrodes, it will substantially reduce the cost to monitor CO2 sequestration. This work was performed under the auspices of the U.S. Department of Energy by University of California Lawrence Livermore National Laboratory under contract No. W-7405-Eng-48.

MEMBRANE PROCESS TO SEQUESTER CO2 FROM POWER PLANT FLUE GAS

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

Tim Merkel; Karl Amo; Richard Baker

2009-03-31

The objective of this project was to assess the feasibility of using a membrane process to capture CO2 from coal-fired power plant flue gas. During this program, MTR developed a novel membrane (Polaris™) with a CO2 permeance tenfold higher than commercial CO2-selective membranes used in natural gas treatment. The Polaris™ membrane, combined with a process design that uses a portion of combustion air as a sweep stream to generate driving force for CO2 permeation, meets DOE post-combustion CO2 capture targets. Initial studies indicate a CO2 separation and liquefaction cost of $20 - $30/ton CO2 using about 15% of the plantmore » energy at 90% CO2 capture from a coal-fired power plant. Production of the Polaris™ CO2 capture membrane was scaled up with MTR’s commercial casting and coating equipment. Parametric tests of cross-flow and countercurrent/sweep modules prepared from this membrane confirm their near-ideal performance under expected flue gas operating conditions. Commercial-scale, 8-inch diameter modules also show stable performance in field tests treating raw natural gas. These findings suggest that membranes are a viable option for flue gas CO2 capture. The next step will be to conduct a field demonstration treating a realworld power plant flue gas stream. The first such MTR field test will capture 1 ton CO2/day at Arizona Public Service’s Cholla coal-fired power plant, as part of a new DOE NETL funded program.« less

Atmospheric mass and the record of liquid water on Mars

NASA Astrophysics Data System (ADS)

Halevy, I.; Head, J. W., III

2017-12-01

Widespread evidence for the action of liquid water on early Mars is generally accepted to require the presence of atmospheric greenhouse agents other than CO2. Much of this activity clusters in the late Noachian and early Hesperian (3.9-3.6 Ga), and appears to coincide with a long maximum in extrusive and explosive volcanic activity. Among other suggestions, a role for S-bearing volcanic gases has been proposed, but these and any other non-CO2 greenhouse gases or atmospheric components require a background CO2 atmosphere of several hundred mbar. Global climate models suggest that even if the surface reservoir of CO2 were much larger than today, this reservoir would be mostly trapped as CO2 ice, and only a few to tens of mbar would be in the atmosphere. Thus, at the long-term steady state, sustained warmth is difficult to achieve in the face of a fainter Sun. We suggest that episodic volcanism released the CO2 trapped as ice at the planet's surface in two ways. First, the emission of S-bearing greenhouse gases (mostly SO2) would lead to warming of a few Kelvins. Second, the deposition of volcanic ash on water and CO2 ice surfaces would push the local energy budget to favor sublimation, and would also decrease the planetary albedo and lead to additional warming. Inflation of the CO2 atmosphere has been shown in global climate models to shift the distribution of snowfall to high elevations, as opposed to a latitude-dependent distribution at low atmospheric pressure. We suggest that seasonal melting of this snow carved the valley networks and filled basin lakes. The duration of warm periods was limited by the timescale for atmospheric collapse by condensation, which is 102-103 years. Repeated inflation episodes over the duration of active volcanism led to an integrated duration of aqueous activity of 106-107 years, enough to carve the valley networks. The S-bearing gases emitted by eruptions formed sulfate minerals, initially uniformly dispersed, then remobilized and locally redeposited at low latitudes during periods of aqueous activity. As volcanic activity waned in the mid-Hesperian, fewer instances of atmospheric inflation occurred, and CO2 was trapped as high-latitude surface ice. Decreasing volcanic input and gradual atmospheric escape ultimately resulted in the remaining reservoir of CO2 observed today.

The oxygen side of sulfate constrains global biospheric productivity in the mid-Phanerozoic

NASA Astrophysics Data System (ADS)

Wing, B. A.

2009-12-01

Recent work has read in the oxygen side of sulfate a record of CO2 concentrations and extreme environments on Neoproterozoic Earth [1, 2]. The connection between CO2 levels and total isotopic composition of mineral proxies for marine sulfate was motivated by an empirical correlation between CO2 concentrations and in 17O anomalies in samples of atmospheric gases preserved as bubbles in ice cores [3,4]. The 17O anomaly in atmospheric O2 has been interpreted to originate primarily from stratospheric photochemical cycles of O3, O2, and CO2 [3, 4]. Both CO2 and O3 form the 17O-enriched partners for the 17O-depleted O2 and, given a fixed atmospheric lifetime for O2, isotopic mass balance dictates that increasing CO2 levels will drive larger relative 17O deficits in O2. With a photochemically-calibrated relationship between the relative 17O anomaly in atmospheric O2 and atmospheric CO2 levels [1], the amount of CO2 in an ancient atmosphere can be directly estimated from the isotopic record of atmospheric O2 bound up in the oxygen side of sulfate. Although they are correlated, the relative 17O anomaly in atmospheric O2 is not only a function of atmospheric CO2 levels. Photosynthetic O2 is characterized by isotopically ‘normal’ oxygen sourced from the global hydrosphere [3]. Increased photosynthetic O2 production, therefore, dilutes the isotopic anomaly found in atmospheric O2. Measurements of the 17O anomaly in O2 from ice cores allow global changes in global biosphere productivity to be traced back to 60 ka ago [3, 4]. Applying similar analysis to recent datasets of the 17O anomaly in marine sulfates [1] and atmospheric CO2 levels [5] produces quantitative global biospheric productivity estimates for the time interval from 310 to 240 Ma ago. Although the time resolution is coarse, much of the mid-Phanerozoic was characterized by global biospheric productivity similar in magnitude to the average global biospheric productivity for the last 10 ka. Counterintuitively, this includes the global mid-Carboniferous biosphere. Global biospheric productivity at the end of the Permian, however, was apparently greatly enhanced relative to the rest of the mid-Phanerozoic. [1] Huiming Bao, J. Lyons, Chuanming Zhou (2008) Nature 453 504. [2] Huiming Bao, I.J. Fairchild, P.M. Wynn, C. Spötl (2009) Science 323 119. [3] B. Luz, E. Barkan, M. L. Bender, M. H. Thiemens, K. A. Boering (1999) Nature 400 547. [4] T. Blunier, B. Barnett, M. L. Bender, M. B. Hendricks (2002) Global Biogeochem. Cycles 16 doi:10.1029/2001GB001460. [5] D. L. Royer (2006) Geochim. Cosmochim. Acta 70 5665.

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

NASA Astrophysics Data System (ADS)

Zickfeld, K.; Tokarska, K.

2014-12-01

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

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

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

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

1984-09-01

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

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

NASA Astrophysics Data System (ADS)

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

2016-02-01

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

Effect of modified atmosphere and vacuum packaging on some quality characteristics and the shelf-life of "morcilla", a typical cooked blood sausage.

PubMed

Cachaldora, Aida; García, Gloria; Lorenzo, José M; García-Fontán, M Camino

2013-02-01

The effect of modified atmosphere and vacuum packaging on the shelf-life of "morcilla", a traditional cooked blood sausage, was investigated. A total of 99 "morcillas" were packaged under vacuum and in modified atmosphere using three different gas mixtures: 15:35:50/O(2):N(2):CO(2) (atmosphere 1), 60:40/N(2):CO(2) (atmosphere 2) and 40:60/N(2):CO(2) (atmosphere 3), and stored during 2, 4, 6 and 8 weeks at 4 °C. Shelf life evaluation was based on pH, water activity (a(w)), colour (CIE L*, a*, b*, C* and h*), TBARS formation and microbial counts. The results indicated that, in general, storage time affected (P<0.05) all parameters whereas no significant differences were observed (P>0.05) among packaging conditions. Based on the microbial counts, the shelf-life of "morcilla" would be greater than 8 weeks for all packaging conditions. Samples packaged with high CO(2) concentrations (40:60/N(2):CO(2)) showed the lowest values of TBARS at the end of storage. Copyright © 2012 Elsevier Ltd. All rights reserved.

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

PubMed

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

2006-12-01

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

Could recent increases in atmospheric CO2 have acted as a selection factor in wild oat populations? Implications for cultivated and wild oat competition

USDA-ARS?s Scientific Manuscript database

Projected increases in atmospheric carbon dioxide concentration, [CO2] may lead to differential selection and competition between weeds and crops. Yet, the current level of atmospheric [CO2] already reflects a rapid rise (~25%) from mid-20th century levels. To assess whether this increase could ha...

Tropospheric O3 compromises net primary production in young stands of trembling aspen, paper birch and sugar maple in response to elevated atmospheric CO2

Treesearch

John S. King; Mark E. Kubiske; Kurt S. Pregitzer; George R. Hendrey; Evan P. McDonald; Christian P. Giardina; Vanessa S. Quinn; David F. Karnosky

2005-01-01

Concentrations of atmospheric CO2 and tropospheric ozone (O3) are rising concurrently in the atmosphere, with potentially antagonistic effects on forest net primary production (NPP) and implications for terrestrial carbon sequestration. Using free-air CO2 enrichment (FACE) technology, we exposed north...

Atmospheric turbulence triggers pronounced diel pattern in karst carbonate geochemistry

NASA Astrophysics Data System (ADS)

Roland, M.; Serrano-Ortiz, P.; Kowalski, A. S.; Goddéris, Y.; Sánchez-Cañete, E. P.; Ciais, P.; Domingo, F.; Cuezva, S.; Sanchez-Moral, S.; Longdoz, B.; Yakir, D.; Van Grieken, R.; Schott, J.; Cardell, C.; Janssens, I. A.

2013-07-01

CO2 exchange between terrestrial ecosystems and the atmosphere is key to understanding the feedbacks between climate change and the land surface. In regions with carbonaceous parent material, CO2 exchange patterns occur that cannot be explained by biological processes, such as disproportionate outgassing during the daytime or nighttime CO2 uptake during periods when all vegetation is senescent. Neither of these phenomena can be attributed to carbonate weathering reactions, since their CO2 exchange rates are too small. Soil ventilation induced by high atmospheric turbulence is found to explain atypical CO2 exchange between carbonaceous systems and the atmosphere. However, by strongly altering subsurface CO2 concentrations, ventilation can be expected to influence carbonate weathering rates. By imposing ventilation-driven CO2 outgassing in a carbonate weathering model, we show here that carbonate geochemistry is accelerated and does play a surprisingly large role in the observed CO2 exchange pattern of a semi-arid ecosystem. We found that by rapidly depleting soil CO2 during the daytime, ventilation disturbs soil carbonate equilibria and therefore strongly magnifies daytime carbonate precipitation and associated CO2 production. At night, ventilation ceases and the depleted CO2 concentrations increase steadily. Dissolution of carbonate is now enhanced, which consumes CO2 and largely compensates for the enhanced daytime carbonate precipitation. This is why only a relatively small effect on global carbonate weathering rates is to be expected. On the short term, however, ventilation has a drastic effect on synoptic carbonate weathering rates, resulting in a pronounced diel pattern that exacerbates the non-biological behavior of soil-atmosphere CO2 exchanges in dry regions with carbonate soils.

Atmospheric CO and hydrogen uptake and CO oxidizer phylogeny for miyake-jima, Japan volcanic deposits.

PubMed

King, Gary M; Weber, Carolyn F; Nanba, Kenji; Sato, Yoshinori; Ohta, Hiroyuki

2008-01-01

We have assayed rates of atmospheric CO and hydrogen uptake, maximum potential CO uptake and the major phylogenetic composition of CO-oxidizing bacterial communities for a variety of volcanic deposits on Miyake-jima, Japan. These deposits represented different ages and stages of plant succession, ranging from unvegetated scoria deposited in 1983 to forest soils on deposits >800 yr old. Atmospheric CO and hydrogen uptake rates varied from -2.0±1.8-6.3±0.1 mg CO m(-2) d(-1) and 0.0±0.4-2.0±0.2 mg H(2) m(-2) d(-1), respectively, and were similar to or greater than values reported for sites on Kilauea volcano, Hawaii, USA. At one of the forested sites, CO was emitted to the atmosphere, while two vegetated sites did not consume atmospheric hydrogen, an unusual observation. Although maximum potential CO uptake rates were also comparable to values for Kilauea, the relationship between these rates and organic carbon contents of scoria or soil indicated that CO oxidizers were relatively more abundant in Miyake-jima deposits. Phylogenetic analyses based on the large sub-unit gene for carbon monoxide dehydrogenase (coxL) indicated that many novel lineages were present on Miyake-jima, that CO-oxidizing Proteobacteria were prevalent in vegetated sites and that community structure appeared to vary more than composition among sites.

Implications of elevated atmospheric CO2 on plant growth and water relations

USDA-ARS?s Scientific Manuscript database

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

Investigating Mars South Residual CO2 Cap with a Global Climate Model

NASA Technical Reports Server (NTRS)

Kahre, M. A.; Dequaire, J.; Hollingsworth, J. L.; Haberle, R. M.

2016-01-01

The CO2 cycle is one of the three controlling climate cycles on Mars. One aspect of the CO2 cycle that is not yet fully understood is the existence of a residual CO2 ice cap that is offset from the south pole. Previous investigations suggest that the atmosphere may control the placement of the south residual cap (e.g., Colaprete et al., 2005). These investigations show that topographically forced stationary eddies in the south during southern hemisphere winter produce colder atmospheric temperatures and increased CO2 snowfall over the hemisphere where the residual cap resides. Since precipitated CO2 ice produces higher surface albedos than directly deposited CO2 ice, it is plausible that CO2 snowfall resulting from the zonally asymmetric atmospheric circulation produces surface ice albedos high enough to maintain a residual cap only in one hemisphere. The goal of the current work is to further evaluate Colaprete et al.'s hypothesis by investigating model-predicted seasonally varying snowfall patterns in the southern polar region and the atmospheric circulation components that control them.

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

NASA Astrophysics Data System (ADS)

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

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

Quality of Golden papaya stored under controlled atmosphere conditions.

PubMed

Martins, Derliane Ribeiro; de Resende, Eder Dutra

2013-10-01

This work evaluated physicochemical parameters of Golden papaya stored under refrigeration in controlled atmospheres. The fruits were kept at 13  in chambers containing either 3 or 6% O2 combined with 6%, 10% or 15% CO2. Moreover, a normal atmosphere was produced with 20.8% O2 and 0.03% CO2 with ethylene scrubbing, and a control treatment was used with ambient conditions. Evaluations were performed at the following times: before storage, after 30 days of storage in controlled atmosphere, and after removal from controlled atmosphere and storage for 7 days in the cold room. At the lower O2 levels and higher CO2 levels, the ripening rate was decreased. The drop in pulp acidity was avoided after 30 days of storage at 3% O2, but the fruits reached normal acidity after removal from controlled atmosphere and storage for 7 days in the cold room. The reducing sugars remained at a higher concentration after 30 days under 3% O2 and 15% CO2 even 7 days after removal from controlled atmosphere and storage in the cold room. This atmosphere also preserved the content of ascorbic acid at a higher level.

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

NASA Astrophysics Data System (ADS)

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

2013-12-01

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

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

NASA Astrophysics Data System (ADS)

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

2009-12-01

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