40 CFR 80.50 - General test procedure requirements for augmentation of the emission models.

Code of Federal Regulations, 2010 CFR

2010-07-01

... § 80.45. (1) VOC, NOX, CO, and CO2 emissions must be measured for all fuel-vehicle combinations tested. (2) Toxics emissions must be measured when testing the extension fuels per the requirements of § 80... PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) REGULATION OF FUELS AND FUEL ADDITIVES Reformulated...

40 CFR 80.50 - General test procedure requirements for augmentation of the emission models.

Code of Federal Regulations, 2012 CFR

2012-07-01

... § 80.45. (1) VOC, NOX, CO, and CO2 emissions must be measured for all fuel-vehicle combinations tested. (2) Toxics emissions must be measured when testing the extension fuels per the requirements of § 80... PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) REGULATION OF FUELS AND FUEL ADDITIVES Reformulated...

40 CFR 80.50 - General test procedure requirements for augmentation of the emission models.

Code of Federal Regulations, 2011 CFR

2011-07-01

... § 80.45. (1) VOC, NOX, CO, and CO2 emissions must be measured for all fuel-vehicle combinations tested. (2) Toxics emissions must be measured when testing the extension fuels per the requirements of § 80... PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) REGULATION OF FUELS AND FUEL ADDITIVES Reformulated...

40 CFR 75.31 - Initial missing data procedures.

Code of Federal Regulations, 2010 CFR

2010-07-01

... 40 Protection of Environment 16 2010-07-01 2010-07-01 false Initial missing data procedures. 75.31... (CONTINUED) CONTINUOUS EMISSION MONITORING Missing Data Substitution Procedures § 75.31 Initial missing data.... For each hour of missing SO2, Hg, or CO2 emissions concentration data (including CO2 data converted...

Analysis of CO2, CO and HC emission reduction in automobiles

NASA Astrophysics Data System (ADS)

Balan, K. N.; Valarmathi, T. N.; Reddy, Mannem Soma Harish; Aravinda Reddy, Gireddy; Sai Srinivas, Jammalamadaka K. M. K.; Vasan

2017-05-01

In the present scenario, the emission from automobiles is becoming a serious problem to the environment. Automobiles, thermal power stations and Industries majorly constitute to the emission of CO2, CO and HC. Though the CO2 available in the atmosphere will be captured by oceans, grasslands; they are not enough to control CO2 present in the atmosphere completely. Also advances in engine and vehicle technology continuously to reduce the emission from engine exhaust are not sufficient to reduce the HC and CO emission. This work concentrates on design, fabrication and analysis to reduce CO2, CO and HC emission from exhaust of automobiles by using molecular sieve 5A of 1.5mm. In this paper, the details of the fabrication, results and discussion about the process are discussed.

40 CFR 98.73 - Calculating GHG emissions.

Code of Federal Regulations, 2010 CFR

2010-07-01

... (CONTINUED) MANDATORY GREENHOUSE GAS REPORTING Ammonia Manufacturing § 98.73 Calculating GHG emissions. You must calculate and report the annual process CO2 emissions from each ammonia manufacturing process unit... ammonia manufacturing unit, the CO2 process emissions from gaseous feedstock according to Equation G-1 of...

40 CFR 98.73 - Calculating GHG emissions.

Code of Federal Regulations, 2014 CFR

2014-07-01

... (CONTINUED) MANDATORY GREENHOUSE GAS REPORTING Ammonia Manufacturing § 98.73 Calculating GHG emissions. You must calculate and report the annual process CO2 emissions from each ammonia manufacturing process unit... ammonia manufacturing unit, the CO2 process emissions from gaseous feedstock according to Equation G-1 of...

40 CFR 98.73 - Calculating GHG emissions.

Code of Federal Regulations, 2013 CFR

2013-07-01

... (CONTINUED) MANDATORY GREENHOUSE GAS REPORTING Ammonia Manufacturing § 98.73 Calculating GHG emissions. You must calculate and report the annual process CO2 emissions from each ammonia manufacturing process unit... ammonia manufacturing unit, the CO2 process emissions from gaseous feedstock according to Equation G-1 of...

40 CFR 98.73 - Calculating GHG emissions.

Code of Federal Regulations, 2011 CFR

2011-07-01

... (CONTINUED) MANDATORY GREENHOUSE GAS REPORTING Ammonia Manufacturing § 98.73 Calculating GHG emissions. You must calculate and report the annual process CO2 emissions from each ammonia manufacturing process unit... ammonia manufacturing unit, the CO2 process emissions from gaseous feedstock according to Equation G-1 of...

40 CFR 98.73 - Calculating GHG emissions.

Code of Federal Regulations, 2012 CFR

2012-07-01

... (CONTINUED) MANDATORY GREENHOUSE GAS REPORTING Ammonia Manufacturing § 98.73 Calculating GHG emissions. You must calculate and report the annual process CO2 emissions from each ammonia manufacturing process unit... ammonia manufacturing unit, the CO2 process emissions from gaseous feedstock according to Equation G-1 of...

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

NASA Astrophysics Data System (ADS)

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

2010-12-01

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

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.

Atmospheric Observations of Carbon Dioxide and Quantification of Fossil Fuel Carbon Dioxide and Emission Inventories using Radiocarbon in the Korean Peninsula during the KORUS-AQ Field Campaign

NASA Astrophysics Data System (ADS)

Choi, Y.; DiGangi, J. P.; Diskin, G. S.; Nowak, J. B.; Halliday, H.; Pusede, S.; Arellano, A. F., Jr.; Tang, W.; Knote, C. J.; Woo, J. H.; Lee, Y.; Kim, Y.; Bu, C.; Blake, D. R.; Simpson, I. J.; Blake, N. J.; Xu, X.

2017-12-01

This presentation discusses a unique data set of airborne in situ carbon dioxide (CO2) and carbon monoxide (CO) soundings and radiocarbon measurements to accurately quantify anthropogenic CO2 emissions from the total measured CO2 signal. Precise assessment of fossil fuel (FF) CO2 gives a better understanding of source contributions to emission inventories in the study region. Fast response (1Hz) and high precision (<0.1 ppm) in situ measurements of atmospheric CO2 and other trace gases, including 60 CO2 radiocarbon measurements from flask samples, onboard the NASA DC-8 aircraft during KORUS-AQ (May-June, 2016), were used in combination with an updated emissions inventory named NIER/KU_CREATE (Comprehensive Regional Emissions inventory for Atmospheric Transport Experiment) to gain a better understanding of pollution characteristics in the study region. Fractional FF CO2 contributions were calculated using radiocarbon and in-situ CO2 concentrations. These quantified FF CO/CO2 ratios from the in situ measurements were compared to the updated emissions inventory. Distinctly higher ratios were found in Chinese outflow, relative to those from the Korean Peninsula, and the emission inventory shows higher CO/CO2 ratios than measurements both in the Korea and China regions. This quantified FF CO/CO2 ratio was applied to continuous measurements of in-situ CO and CO2 and used to identify the portion of biogenic CO2 observed during the field campaign (the biospheric contribution to the total CO2 is typically 20-30 % in this regions). This continuous partitioning of biogenic and anthropogenic sources will give a better understanding of diurnal variations of local sources and will be helpful for the evaluation of emission inventories, where mega-city fossil fuel combustion sources mix with biospheric sources. Also discussed is the comparison of quantified FF CO/CO2 ratios with the CAMS (Copernicus Atmosphere Monitoring Service) simulated products ratios and local source contribution analysis using FLEXPART-WRF back-trajectory analysis to understand the source of variability of FF CO/CO2 ratios in the study regions.

Measurements of Greenhouse Gases around the Sacramento Area: The Airborne Greenhouse Emissions Survey (AGES) Campaign

NASA Astrophysics Data System (ADS)

Karion, A.; Fischer, M. L.; Turnbull, J. C.; Sweeney, C.; Faloona, I. C.; Zagorac, N.; Guilderson, T. P.; Saripalli, S.; Sherwood, T.

2009-12-01

The state of California is leading the United States by enacting legislation (AB-32) to reduce greenhouse gas emissions to 1990 levels by 2020. The success of reduction efforts can be gauged with accurate emissions inventories and potentially verified with atmospheric measurements of greenhouse gases (GHGs) over time. Measurements of multiple GHGs and associated trace gas species in a specific region also provide information on emissions ratios for source apportionment. We conducted the Airborne Greenhouse Emissions Survey (AGES) campaign to determine emissions signature ratios for the sources that exist in the San Francisco Bay and Sacramento Valley areas. Specifically, we attempt to determine the emissions signatures of sources that influence ongoing measurements made at a tall-tower measurement site near Walnut Grove, CA. For two weeks in February and March of 2009, a Cessna 210 was flown throughout the Sacramento region, making continuous measurements of CO2, CH4, and CO while also sampling discrete flasks for a variety of additional tracers, including SF6, N2O, and 14C in CO2 (Δ14CO2). Flight paths were planned using wind predictions for each day to maximize sampling of sources whose emissions would also be sampled contemporaneously by the instrumentation at the Walnut Grove tower (WGC), part of the ongoing California Greenhouse Gas Emissions Measurement (CALGEM) project between NOAA/ESRL’s Carbon Cycle group and Lawrence Berkeley National Laboratory (LBNL). Flights were performed in two distinct patterns: 1) flying across a plume upwind and downwind of the Sacramento urban area, and 2) flying across the Sacramento-San Joaquin Delta from Richmond to Walnut Grove, a region consisting of natural wetlands as well as several power plants and refineries. Results show a variety of well-correlated mixing ratio signals downwind of Sacramento, documenting the urban signature emission ratios, while emissions ratios in the Delta region were more variable, likely due to the both natural and anthropogenic sources in that region. Periodic flask measurements of Δ14CO2 provide additional insight regarding the partitioning of CO2 emissions due to fossil fuel (deficient in 14C) from those of biospheric sources. A strong correlation between fossil-fuel CO2 and CO was measured downwind of Sacramento, suggesting that the continuous measurements of CO can be used to estimate a continuous profile of fossil-fuel CO2 enhancement in this region.

40 CFR 75.57 - General recordkeeping provisions.

Code of Federal Regulations, 2014 CFR

2014-07-01

... stack gas (percent H2O, rounded to the nearest tenth). If the continuous moisture monitoring system... record daily the following information for CO2 mass emissions: (i) Date; (ii) Daily combustion-formed CO2... whether optional procedure to adjust combustion-formed CO2 mass emissions for carbon retained in flyash...

40 CFR 75.57 - General recordkeeping provisions.

Code of Federal Regulations, 2013 CFR

2013-07-01

... stack gas (percent H2O, rounded to the nearest tenth). If the continuous moisture monitoring system... record daily the following information for CO2 mass emissions: (i) Date; (ii) Daily combustion-formed CO2... whether optional procedure to adjust combustion-formed CO2 mass emissions for carbon retained in flyash...

40 CFR 75.57 - General recordkeeping provisions.

Code of Federal Regulations, 2011 CFR

2011-07-01

... stack gas (percent H2O, rounded to the nearest tenth). If the continuous moisture monitoring system... record daily the following information for CO2 mass emissions: (i) Date; (ii) Daily combustion-formed CO2... whether optional procedure to adjust combustion-formed CO2 mass emissions for carbon retained in flyash...

40 CFR 75.57 - General recordkeeping provisions.

Code of Federal Regulations, 2012 CFR

2012-07-01

... stack gas (percent H2O, rounded to the nearest tenth). If the continuous moisture monitoring system... record daily the following information for CO2 mass emissions: (i) Date; (ii) Daily combustion-formed CO2... whether optional procedure to adjust combustion-formed CO2 mass emissions for carbon retained in flyash...

Evaluation and Optimization of China's Anthropogenic CO2 Emissions using Observations from Northern China (2005-2009).

NASA Astrophysics Data System (ADS)

Dayalu, A.; Munger, J. W.; Wang, Y.; Wofsy, S.; Zhao, Y.; Nielsen, C. P.; Nehrkorn, T.; McElroy, M. B.; Chang, R.

2017-12-01

China has pledged to peak carbon emissions by 2030, but there continues to be significant uncertainty in estimates of its anthropogenic carbon dioxide (CO2) emissions. In this study, we evaluate the performance of three anthropogenic CO2 inventories, two global and one regional, using five years of continuous hourly observations from a site in Northern China. We model five years of continuous hourly observations (2005 to 2009) using the Stochastic Time-Inverted Lagrangian Transport Model (STILT) run in backward time mode driven by high resolution meteorology from the Weather Research and Forecasting Model version 3.6.1 (WRF) with vegetation fluxes prescribed by a simple biosphere model. We calculate regional enhancements to advected background CO2 derived from NOAA CarbonTracker on seasonal and annual bases and use observations to optimize emissions inventories within the site's influence region at these timescales. Finally, we use annual enhancements to examine carbon intensity of provinces in and adjacent to Northern China as CO2 per unit of the region's GDP to evaluate the effects of local and global economic events on CO2 emissions. With the exception of peak growing season where discrepancies are confounded by errors in the vegetation model, we find the regional inventory agrees significantly better with observations than the global inventories at all timescales. Here we use a single measurement site; significant improvements in inventory optimizations can be achieved with a network of measurements stations. This study highlights the importance of China-specific data over global averages in emissions evaluation and demonstrates the value of top-down studies in independently evaluating inventory performance. We demonstrate the framework's ability to resolve differences of at least 20% among inventories, establishing a benchmark for ongoing efforts to decrease uncertainty in China's reported CO2 emissions estimates.

40 CFR 1037.105 - Exhaust emission standards for CO2 for vocational vehicles.

Code of Federal Regulations, 2013 CFR

2013-07-01

... (CONTINUED) AIR POLLUTION CONTROLS CONTROL OF EMISSIONS FROM NEW HEAVY-DUTY MOTOR VEHICLES Emission Standards... CO2 standard (g/ton-mile) for model year 2017 and later GVWR ≤ 19,500 388 373 19,500 < GVWR ≤ 33,000...

40 CFR 1037.105 - Exhaust emission standards for CO2 for vocational vehicles.

Code of Federal Regulations, 2012 CFR

2012-07-01

... (CONTINUED) AIR POLLUTION CONTROLS CONTROL OF EMISSIONS FROM NEW HEAVY-DUTY MOTOR VEHICLES Emission Standards... CO2 standard (g/ton-mile) for model year 2017 and later GVWR ≤ 19,500 388 373 19,500 < GVWR ≤ 33,000...

40 CFR 1037.105 - Exhaust emission standards for CO2 for vocational vehicles.

Code of Federal Regulations, 2014 CFR

2014-07-01

... (CONTINUED) AIR POLLUTION CONTROLS CONTROL OF EMISSIONS FROM NEW HEAVY-DUTY MOTOR VEHICLES Emission Standards... CO2 standard (g/ton-mile) for model year 2017 and later GVWR ≤19,500 388 373 19,500

Greenhouse gas emissions of different land uses in the delta region of Red River, Vietnam

NASA Astrophysics Data System (ADS)

Zhou, Minghua; Ha, Thu; An, Ngo The; Brüggemann, Nicolas

2017-04-01

Agricultural activities are responsible for up to a third of total anthropogenic GHG emissions. The subtropical/tropical delta areas of the large rivers in Southeast Asia are long-term history agricultural regions in the world. However, due to lack of field measurements, the estimation of the contribution of agro-ecosystems in the subtropical/tropical delta areas to global greenhouse gas emissions remains largely uncertain. Here, we conducted field experiments since January 2016 to quantify greenhouse gases (CO2, CH4 and N2O) emissions from four agricultural land uses of annual rice-rice, rice-vegetable, continuous vegetable system and fish pond in Red River delta region of Vietnam by using the transparent static chamber-gas chromatography technique. Higher N2O emissions were observed in the rice-vegetable and continuous vegetable systems, while lower N2O emissions were observed in the rice-rice and find pond systems. Compared to rice-rice system the cumulative N2O fluxes were on average twenty-fold higher in the rice-vegetable and continuous vegetable systems but significantly lower (75%) in the fish pond. Overall the net CO2 sinks were observed in the rice-rice system while other three land uses of rice-vegetable, continuous vegetable and fish pond acted as the net CO2 sources. The rice-rice and fish pond showed net CH4 emissions while variations of CH4 emissions (i.e. shifting between sources and sinks) along variations of soil moisture and temperature were observed in rice-vegetable and continuous vegetable systems. Compared to rice-rice system, the cumulative CH4 fluxes were significantly decreased by 100% for continuous vegetable system, 94% for rice-vegetable system and 89% for fish pond. Overall, the data suggest that conversion of traditional rice-rice paddy system to rice-vegetable, continuous vegetable system and find pond, which are currently undergoing driven by the economical requests and environmental changes (e.g., salinity intrusion) in this delta region, could alter CH4, CO2 and N2O emissions.

40 CFR Table 5 to Subpart Ppppp of... - Continuous Compliance With Emission Limitations

Code of Federal Regulations, 2010 CFR

2010-07-01

... THC concentration emission limitation a. Demonstrate CO or THC emissions are 20 ppmvd or less over..., according to § 63.9320; 2. CO or THC percent reduction emission limitation a. Demonstrate a reduction in CO or THC of 96 percent or more over each 4-hour rolling averaging period i. Collecting the CPMS data...

40 CFR Table 5 to Subpart Ppppp of... - Continuous Compliance With Emission Limitations

Code of Federal Regulations, 2012 CFR

2012-07-01

... THC concentration emission limitation a. Demonstrate CO or THC emissions are 20 ppmvd or less over..., according to § 63.9320; 2. CO or THC percent reduction emission limitation a. Demonstrate a reduction in CO or THC of 96 percent or more over each 4-hour rolling averaging period i. Collecting the CPMS data...

40 CFR Table 5 to Subpart Ppppp of... - Continuous Compliance With Emission Limitations

Code of Federal Regulations, 2013 CFR

2013-07-01

... THC concentration emission limitation a. Demonstrate CO or THC emissions are 20 ppmvd or less over..., according to § 63.9320; 2. CO or THC percent reduction emission limitation a. Demonstrate a reduction in CO or THC of 96 percent or more over each 4-hour rolling averaging period i. Collecting the CPMS data...

40 CFR Table 5 to Subpart Ppppp of... - Continuous Compliance With Emission Limitations

Code of Federal Regulations, 2011 CFR

2011-07-01

... THC concentration emission limitation a. Demonstrate CO or THC emissions are 20 ppmvd or less over..., according to § 63.9320; 2. CO or THC percent reduction emission limitation a. Demonstrate a reduction in CO or THC of 96 percent or more over each 4-hour rolling averaging period i. Collecting the CPMS data...

40 CFR Table 5 to Subpart Ppppp of... - Continuous Compliance With Emission Limitations

Code of Federal Regulations, 2014 CFR

2014-07-01

... THC concentration emission limitation a. Demonstrate CO or THC emissions are 20 ppmvd or less over..., according to § 63.9320; 2. CO or THC percent reduction emission limitation a. Demonstrate a reduction in CO or THC of 96 percent or more over each 4-hour rolling averaging period i. Collecting the CPMS data...

40 CFR 89.417 - Data evaluation for gaseous emissions.

Code of Federal Regulations, 2014 CFR

2014-07-01

... PROGRAMS (CONTINUED) CONTROL OF EMISSIONS FROM NEW AND IN-USE NONROAD COMPRESSION-IGNITION ENGINES Exhaust... emission recording, the last 60 seconds of each mode are recorded, and the average values for HC, CO, CO2...

40 CFR 89.417 - Data evaluation for gaseous emissions.

Code of Federal Regulations, 2011 CFR

2011-07-01

... PROGRAMS (CONTINUED) CONTROL OF EMISSIONS FROM NEW AND IN-USE NONROAD COMPRESSION-IGNITION ENGINES Exhaust... emission recording, the last 60 seconds of each mode are recorded, and the average values for HC, CO, CO2...

40 CFR 89.417 - Data evaluation for gaseous emissions.

Code of Federal Regulations, 2010 CFR

2010-07-01

... PROGRAMS (CONTINUED) CONTROL OF EMISSIONS FROM NEW AND IN-USE NONROAD COMPRESSION-IGNITION ENGINES Exhaust... emission recording, the last 60 seconds of each mode are recorded, and the average values for HC, CO, CO2...

40 CFR 89.417 - Data evaluation for gaseous emissions.

Code of Federal Regulations, 2012 CFR

2012-07-01

... PROGRAMS (CONTINUED) CONTROL OF EMISSIONS FROM NEW AND IN-USE NONROAD COMPRESSION-IGNITION ENGINES Exhaust... emission recording, the last 60 seconds of each mode are recorded, and the average values for HC, CO, CO2...

40 CFR 89.417 - Data evaluation for gaseous emissions.

Code of Federal Regulations, 2013 CFR

2013-07-01

... PROGRAMS (CONTINUED) CONTROL OF EMISSIONS FROM NEW AND IN-USE NONROAD COMPRESSION-IGNITION ENGINES Exhaust... emission recording, the last 60 seconds of each mode are recorded, and the average values for HC, CO, CO2...

Greenhouse gas and ammonia emissions from production of compost bedding on a dairy farm.

PubMed

Fillingham, M A; VanderZaag, A C; Burtt, S; Baldé, H; Ngwabie, N M; Smith, W; Hakami, A; Wagner-Riddle, C; Bittman, S; MacDonald, D

2017-12-01

Recent developments in composting technology enable dairy farms to produce their own bedding from composted manure. This management practice alters the fate of carbon and nitrogen; however, there is little data available documenting how gaseous emissions are impacted. This study measured in-situ emissions of methane (CH 4 ), carbon dioxide (CO 2 ), nitrous oxide (N 2 O), and ammonia (NH 3 ) from an on-farm solid-liquid separation system followed by continuously-turned plug-flow composting over three seasons. Emissions were measured separately from the continuously-turned compost phase, and the compost-storage phase prior to the compost being used for cattle bedding. Active composting had low emissions of N 2 O and CH 4 with most carbon being emitted as CO 2 -C and most N emitted as NH 3 -N. Compost storage had higher CH 4 and N 2 O emissions than the active phase, while NH 3 was emitted at a lower rate, and CO 2 was similar. Overall, combining both the active composting and storage phases, the mean total emissions were 3.9×10 -2 gCH 4 kg -1 raw manure (RM), 11.3gCO 2 kg -1 RM, 2.5×10 -4 g N 2 O kg -1 RM, and 0.13g NH 3 kg -1 RM. Emissions with solid-separation and composting were compared to calculated emissions for a traditional (unseparated) liquid manure storage tank. The total greenhouse gas emissions (CH 4 +N 2 O) from solid separation, composting, compost storage, and separated liquid storage were reduced substantially on a CO 2 -equivalent basis compared to traditional liquid storage. Solid-liquid separation and well-managed composting could mitigate overall greenhouse gas emissions; however, an environmental trade off was that NH 3 was emitted at higher rates from the continuously turned composter than reported values for traditional storage. Crown Copyright © 2017. Published by Elsevier Ltd. All rights reserved.

China's transportation energy consumption and CO2 emissions from a global perspective

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

Yin, Xiang; Chen, Wenying; Eom, Jiyong

2015-07-01

ABSTRACT Rapidly growing energy demand from China's transportation sector in the last two decades have raised concerns over national energy security, local air pollution, and carbon dioxide (CO2) emissions, and there is broad consensus that China's transportation sector will continue to grow in the coming decades. This paper explores the future development of China's transportation sector in terms of service demands, final energy consumption, and CO2 emissions, and their interactions with global climate policy. This study develops a detailed China transportation energy model that is nested in an integrated assessment model—Global Change Assessment Model (GCAM)—to evaluate the long-term energy consumptionmore » and CO2 emissions of China's transportation sector from a global perspective. The analysis suggests that, without major policy intervention, future transportation energy consumption and CO2 emissions will continue to rapidly increase and the transportation sector will remain heavily reliant on fossil fuels. Although carbon price policies may significantly reduce the sector's energy consumption and CO2 emissions, the associated changes in service demands and modal split will be modest, particularly in the passenger transport sector. The analysis also suggests that it is more difficult to decarbonize the transportation sector than other sectors of the economy, primarily owing to its heavy reliance on petroleum products.« less

Emission factors and characteristics of ammonia, hydrogen sulfide, carbon dioxide, and particulate matter at two high-rise layer hen houses

NASA Astrophysics Data System (ADS)

Ni, Ji-Qin; Liu, Shule; Diehl, Claude A.; Lim, Teng-Teeh; Bogan, Bill W.; Chen, Lide; Chai, Lilong; Wang, Kaiying; Heber, Albert J.

2017-04-01

Air pollutants emitted from confined animal buildings can cause environmental pollution and ecological damage. Long-term (>6 months) and continuous (or high frequency) monitoring that can reveal seasonal and diurnal variations is needed to obtain emission factors and characteristics about these pollutants. A two-year continuous monitoring of ammonia (NH3), hydrogen sulfide (H2S), carbon dioxide (CO2) and particulate matter (PM10) emissions from two 218,000-hen high-rise layer houses (H-A and H-B) in Indiana, USA was conducted from June 2007 to May 2009. Gaseous pollutant concentrations were measured with two gas analyzers and PM10 concentrations were measured with three Tapered Element Oscillating Microbalances. The operation and performance of ventilation fans were continuously monitored with multiple methods. Only the emission rates calculated with valid data days (days with more than 18 h, or 75%, of valid data) are reported in this paper. The two-house and two-year mean ± standard deviation emissions per day per hen for NH3, H2S, CO2, and PM10 were 1.08 ± 0.42 g, 1.37 ± 0.83 mg, 76.7 ± 14.6 g, and 20.6 ± 22.5 mg, respectively. Seasonal emission variations were demonstrated for NH3 and CO2, but not evident for H2S and PM10. Ammonia and CO2 emissions were higher in winter than in summer. Significant daily mean emission variations were observed for all four pollutants between the two houses (P < 0.05), and between the two years from the same house (P < 0.01) except for CO2 at one house. Carbon dioxide originated from manure decomposition was >9% of that from bird respiration. Emissions of CO2 during molting were about 80% of those during normal egg production days. Emissions of H2S were not a major concern due to their very low quantities. Emissions of PM10 were more variable than other pollutants. However, not all of the emission statistics are explainable.

40 CFR 86.316-79 - Carbon monoxide and carbon dioxide analyzer specifications.

Code of Federal Regulations, 2010 CFR

2010-07-01

... AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) CONTROL OF EMISSIONS FROM NEW AND IN-USE HIGHWAY VEHICLES AND...) The use of linearizing circuits is permitted. (c) The minimum water rejection ratio (maximum CO 2...) The minimum CO 2 rejection ratio (maximum CO 2 interference) as measured by § 86.322 for CO analyzers...

40 CFR 98.143 - Calculating GHG emissions.

Code of Federal Regulations, 2011 CFR

2011-07-01

... (CONTINUED) MANDATORY GREENHOUSE GAS REPORTING Glass Production § 98.143 Calculating GHG emissions. You must calculate and report the annual process CO2 emissions from each continuous glass melting furnace using the procedure in paragraphs (a) and (b) of this section. (a) For each continuous glass melting furnace that...

40 CFR 98.143 - Calculating GHG emissions.

Code of Federal Regulations, 2010 CFR

2010-07-01

... (CONTINUED) MANDATORY GREENHOUSE GAS REPORTING Glass Production § 98.143 Calculating GHG emissions. You must calculate and report the annual process CO2 emissions from each continuous glass melting furnace using the procedure in paragraphs (a) and (b) of this section. (a) For each continuous glass melting furnace that...

40 CFR 86.322-79 - NDIR CO2 rejection ratio check.

Code of Federal Regulations, 2012 CFR

2012-07-01

... 40 Protection of Environment 19 2012-07-01 2012-07-01 false NDIR CO2 rejection ratio check. 86.322... PROGRAMS (CONTINUED) CONTROL OF EMISSIONS FROM NEW AND IN-USE HIGHWAY VEHICLES AND ENGINES Emission....322-79 NDIR CO2 rejection ratio check. (a) Zero and span the analyzer on the lowest range that will be...

40 CFR 86.322-79 - NDIR CO2 rejection ratio check.

Code of Federal Regulations, 2013 CFR

2013-07-01

... 40 Protection of Environment 19 2013-07-01 2013-07-01 false NDIR CO2 rejection ratio check. 86.322... PROGRAMS (CONTINUED) CONTROL OF EMISSIONS FROM NEW AND IN-USE HIGHWAY VEHICLES AND ENGINES Emission....322-79 NDIR CO2 rejection ratio check. (a) Zero and span the analyzer on the lowest range that will be...

40 CFR 86.322-79 - NDIR CO2 rejection ratio check.

Code of Federal Regulations, 2011 CFR

2011-07-01

... 40 Protection of Environment 18 2011-07-01 2011-07-01 false NDIR CO2 rejection ratio check. 86.322... PROGRAMS (CONTINUED) CONTROL OF EMISSIONS FROM NEW AND IN-USE HIGHWAY VEHICLES AND ENGINES Emission....322-79 NDIR CO2 rejection ratio check. (a) Zero and span the analyzer on the lowest range that will be...

40 CFR 86.322-79 - NDIR CO2 rejection ratio check.

Code of Federal Regulations, 2010 CFR

2010-07-01

... 40 Protection of Environment 18 2010-07-01 2010-07-01 false NDIR CO2 rejection ratio check. 86.322... PROGRAMS (CONTINUED) CONTROL OF EMISSIONS FROM NEW AND IN-USE HIGHWAY VEHICLES AND ENGINES Emission....322-79 NDIR CO2 rejection ratio check. (a) Zero and span the analyzer on the lowest range that will be...

40 CFR 86.1540 - Idle exhaust sample analysis.

Code of Federal Regulations, 2014 CFR

2014-07-01

... (CONTINUED) CONTROL OF EMISSIONS FROM NEW AND IN-USE HIGHWAY VEHICLES AND ENGINES Emission Regulations for... CVS sampling system is used, the analysis procedures for dilute CO and CO2 specified in 40 CFR part 1065 apply. Follow the raw CO2 analysis procedure specified in 40 CFR part 1065, subpart F, for the raw...

Estimation of CO2 emissions from waste incinerators: Comparison of three methods.

PubMed

Lee, Hyeyoung; Yi, Seung-Muk; Holsen, Thomas M; Seo, Yong-Seok; Choi, Eunhwa

2018-03-01

Climate-relevant CO 2 emissions from waste incineration were compared using three methods: making use of CO 2 concentration data, converting O 2 concentration and waste characteristic data, and using a mass balance method following Intergovernmental Panel on Climate Change (IPCC) guidelines. For the first two methods, CO 2 and O 2 concentrations were measured continuously from 24 to 86 days. The O 2 conversion method in comparison to the direct CO 2 measurement method had a 4.8% mean difference in daily CO 2 emissions for four incinerators where analyzed waste composition data were available. However, the IPCC method had a higher difference of 13% relative to the direct CO 2 measurement method. For three incinerators using designed values for waste composition, the O 2 conversion and IPCC methods in comparison to the direct CO 2 measurement method had mean differences of 7.5% and 89%, respectively. Therefore, the use of O 2 concentration data measured for monitoring air pollutant emissions is an effective method for estimating CO 2 emissions resulting from waste incineration. Copyright © 2017 Elsevier Ltd. All rights reserved.

40 CFR 86.159-08 - Exhaust emission test procedures for US06 emissions.

Code of Federal Regulations, 2013 CFR

2013-07-01

... gasoline-fueled Otto-cycle vehicles, the composite samples collected in bags are analyzed for THC, CO, CO2, CH4, and NOX. For petroleum-fueled diesel-cycle vehicles, THC is sampled and analyzed continuously according to the provisions of § 86.110. Parallel bag samples of dilution air are analyzed for THC, CO, CO2...

40 CFR 86.160-00 - Exhaust emission test procedure for SC03 emissions.

Code of Federal Regulations, 2014 CFR

2014-07-01

... collected in bags are analyzed for THC, CO, CO2, CH4, and NOX. For petroleum-fueled diesel-cycle vehicles, THC is sampled and analyzed continuously according to the provisions of § 86.110. Parallel bag samples of dilution air are analyzed for THC, CO, CO2, CH4, and NOX. (b) Dynamometer activities. (1) All...

40 CFR 86.160-00 - Exhaust emission test procedure for SC03 emissions.

Code of Federal Regulations, 2012 CFR

2012-07-01

... collected in bags are analyzed for THC, CO, CO2, CH4, and NOX. For petroleum-fueled diesel-cycle vehicles, THC is sampled and analyzed continuously according to the provisions of § 86.110. Parallel bag samples of dilution air are analyzed for THC, CO, CO2, CH4, and NOX. (b) Dynamometer activities. (1) All...

40 CFR 86.159-08 - Exhaust emission test procedures for US06 emissions.

Code of Federal Regulations, 2014 CFR

2014-07-01

... gasoline-fueled Otto-cycle vehicles, the composite samples collected in bags are analyzed for THC, CO, CO2, CH4, and NOX. For petroleum-fueled diesel-cycle vehicles, THC is sampled and analyzed continuously according to the provisions of § 86.110. Parallel bag samples of dilution air are analyzed for THC, CO, CO2...

40 CFR 86.159-08 - Exhaust emission test procedures for US06 emissions.

Code of Federal Regulations, 2011 CFR

2011-07-01

... gasoline-fueled Otto-cycle vehicles, the composite samples collected in bags are analyzed for THC, CO, CO2, CH4, and NOX. For petroleum-fueled diesel-cycle vehicles, THC is sampled and analyzed continuously according to the provisions of § 86.110. Parallel bag samples of dilution air are analyzed for THC, CO, CO2...

40 CFR 86.159-08 - Exhaust emission test procedures for US06 emissions.

Code of Federal Regulations, 2010 CFR

2010-07-01

... gasoline-fueled Otto-cycle vehicles, the composite samples collected in bags are analyzed for THC, CO, CO2, CH4, and NOX. For petroleum-fueled diesel-cycle vehicles, THC is sampled and analyzed continuously according to the provisions of § 86.110. Parallel bag samples of dilution air are analyzed for THC, CO, CO2...

40 CFR 86.160-00 - Exhaust emission test procedure for SC03 emissions.

Code of Federal Regulations, 2013 CFR

2013-07-01

... collected in bags are analyzed for THC, CO, CO2, CH4, and NOX. For petroleum-fueled diesel-cycle vehicles, THC is sampled and analyzed continuously according to the provisions of § 86.110. Parallel bag samples of dilution air are analyzed for THC, CO, CO2, CH4, and NOX. (b) Dynamometer activities. (1) All...

40 CFR 86.159-08 - Exhaust emission test procedures for US06 emissions.

Code of Federal Regulations, 2012 CFR

2012-07-01

... gasoline-fueled Otto-cycle vehicles, the composite samples collected in bags are analyzed for THC, CO, CO2, CH4, and NOX. For petroleum-fueled diesel-cycle vehicles, THC is sampled and analyzed continuously according to the provisions of § 86.110. Parallel bag samples of dilution air are analyzed for THC, CO, CO2...

40 CFR 63.9307 - What are my continuous emissions monitoring system installation, operation, and maintenance...

Code of Federal Regulations, 2013 CFR

2013-07-01

... install, operate, and maintain each CEMS to monitor carbon monoxide (CO) or total hydrocarbons (THC) and... emission control device. (b) To comply with the CO or THC percent reduction emission limitation, you may install, operate, and maintain a CEMS to monitor CO or THC and O2 at both the inlet and the outlet of the...

40 CFR 63.9307 - What are my continuous emissions monitoring system installation, operation, and maintenance...

Code of Federal Regulations, 2014 CFR

2014-07-01

... install, operate, and maintain each CEMS to monitor carbon monoxide (CO) or total hydrocarbons (THC) and... emission control device. (b) To comply with the CO or THC percent reduction emission limitation, you may install, operate, and maintain a CEMS to monitor CO or THC and O2 at both the inlet and the outlet of the...

40 CFR 63.9307 - What are my continuous emissions monitoring system installation, operation, and maintenance...

Code of Federal Regulations, 2012 CFR

2012-07-01

... install, operate, and maintain each CEMS to monitor carbon monoxide (CO) or total hydrocarbons (THC) and... emission control device. (b) To comply with the CO or THC percent reduction emission limitation, you may install, operate, and maintain a CEMS to monitor CO or THC and O2 at both the inlet and the outlet of the...

40 CFR 63.9307 - What are my continuous emissions monitoring system installation, operation, and maintenance...

Code of Federal Regulations, 2010 CFR

2010-07-01

... install, operate, and maintain each CEMS to monitor carbon monoxide (CO) or total hydrocarbons (THC) and... emission control device. (b) To comply with the CO or THC percent reduction emission limitation, you may install, operate, and maintain a CEMS to monitor CO or THC and O2 at both the inlet and the outlet of the...

40 CFR 63.9307 - What are my continuous emissions monitoring system installation, operation, and maintenance...

Code of Federal Regulations, 2011 CFR

2011-07-01

... install, operate, and maintain each CEMS to monitor carbon monoxide (CO) or total hydrocarbons (THC) and... emission control device. (b) To comply with the CO or THC percent reduction emission limitation, you may install, operate, and maintain a CEMS to monitor CO or THC and O2 at both the inlet and the outlet of the...

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.

Detecting fossil fuel emissions patterns from subcontinental regions using North American in situ CO2 measurements.

PubMed

Shiga, Yoichi P; Michalak, Anna M; Gourdji, Sharon M; Mueller, Kim L; Yadav, Vineet

2014-06-28

The ability to monitor fossil fuel carbon dioxide (FFCO 2 ) emissions from subcontinental regions using atmospheric CO 2 observations remains an important but unrealized goal. Here we explore a necessary but not sufficient component of this goal, namely, the basic question of the detectability of FFCO 2 emissions from subcontinental regions. Detectability is evaluated by examining the degree to which FFCO 2 emissions patterns from specific regions are needed to explain the variability observed in high-frequency atmospheric CO 2 observations. Analyses using a CO 2 monitoring network of 35 continuous measurement towers over North America show that FFCO 2 emissions are difficult to detect during nonwinter months. We find that the compounding effects of the seasonality of atmospheric transport patterns and the biospheric CO 2 flux signal dramatically hamper the detectability of FFCO 2 emissions. Results from several synthetic data case studies highlight the need for advancements in data coverage and transport model accuracy if the goal of atmospheric measurement-based FFCO 2 emissions detection and estimation is to be achieved beyond urban scales. Poor detectability of fossil fuel CO 2 emissions from subcontinental regionsDetectability assessed via attribution of emissions patterns in atmospheric dataLoss in detectability due to transport modeling errors and biospheric signal.

Framework for Assessing Biogenic CO2 Emissions from ...

EPA Pesticide Factsheets

This revision of the 2011 report, Accounting Framework for Biogenic CO2 Emissions from Stationary Sources, evaluates biogenic CO2 emissions from stationary sources, including a detailed study of the scientific and technical issues associated with assessing biogenic carbon dioxide emissions from stationary sources. EPA developed the revised report, Framework for Assessing Biogenic CO2 Emissions from Stationary Sources, to present a methodological framework for assessing the extent to which the production, processing, and use of biogenic material at stationary sources for energy production results in a net atmospheric contribution of biogenic CO2 emissions. Biogenic carbon dioxide emissions are defined as CO2 emissions related to the natural carbon cycle, as well as those resulting from the production, harvest, combustion, digestion, decomposition, and processing of biologically-based materials. The EPA is continuing to refine its technical assessment of biogenic CO2 emissions through another round of targeted peer review of the revised study with the EPA Science Advisory Board (SAB). This study was submitted to the SAB's Biogenic Carbon Emissions Panel in February 2015. http://yosemite.epa.gov/sab/sabproduct.nsf/0/3235dac747c16fe985257da90053f252!OpenDocument&TableRow=2.2#2 The revised report will inform efforts by policymakers, academics, and other stakeholders to evaluate the technical aspects related to assessments of biogenic feedstocks used for energy at s

40 CFR 1037.106 - Exhaust emission standards for CO2 for tractors above 26,000 pounds GVWR.

Code of Federal Regulations, 2013 CFR

2013-07-01

... PROTECTION AGENCY (CONTINUED) AIR POLLUTION CONTROLS CONTROL OF EMISSIONS FROM NEW HEAVY-DUTY MOTOR VEHICLES... standard (g/ton-mile) for model years 2014-2016 CO2 standard (g/ton-mile) for model year 2017 and later 26...

40 CFR 1037.106 - Exhaust emission standards for CO2 for tractors above 26,000 pounds GVWR.

Code of Federal Regulations, 2014 CFR

2014-07-01

... PROTECTION AGENCY (CONTINUED) AIR POLLUTION CONTROLS CONTROL OF EMISSIONS FROM NEW HEAVY-DUTY MOTOR VEHICLES... standard (g/ton-mile) for model years 2014-2016 CO2 standard (g/ton-mile) for model year 2017 and later 26...

40 CFR 1037.106 - Exhaust emission standards for CO2 for tractors above 26,000 pounds GVWR.

Code of Federal Regulations, 2012 CFR

2012-07-01

... PROTECTION AGENCY (CONTINUED) AIR POLLUTION CONTROLS CONTROL OF EMISSIONS FROM NEW HEAVY-DUTY MOTOR VEHICLES... standard (g/ton-mile) for model years 2014-2016 CO2 standard (g/ton-mile) for model year 2017 and later 26...

Constructing a sustainable power sector in China: current and future emissions of coal-fired power plants from 2010 to 2030

NASA Astrophysics Data System (ADS)

Tong, D.; Zhang, Q.

2017-12-01

As the largest energy infrastructure in China, power sector consumed more coal than any other sector and threatened air quality and greenhouse gas (GHG) abatement target. In this work, we assessed the evolution of coal-fired power plants in China during 2010-2030 and the evolution of associated emissions for the same period by using a unit-based emission projection model which integrated the historical power plants information, turnover of the future power plant fleet, and the evolution of end-of-pipe control technologies. We found that, driven by the stringent environmental legislation, SO2, NOx, and PM2.5 emissions from China's coal-fired power plants decreased by 49%, 45%, and 24% respectively during 2010-2015, comparing to 14% increase of coal consumption and 15% increase in CO2 emissions. We estimated that under current national energy development planning, coal consumption and CO2 emissions from coal-fired power plants will continue to increase until 2030, in which against the China's Intended Nationally Determined Contributions (INDCs) targets. Early retirement of old and low-efficient power plants will cumulatively reduce 2.2 Pg CO2 emissions from the baseline scenario during 2016-2030, but still could not curb CO2 emissions from the peak before 2030. Owing to the implementation of "near zero" emission control policy, we projected that emissions of air pollutants will significantly decrease during the same period under all scenarios, indicating the decoupling trends of air pollutants and CO2 emissions. Although with limited direct emission reduction benefits, increasing operating hours of power plants could avoid 236 GW of new power plants construction, which could indirectly reduce emissions embodied in the construction activity. Our results identified a more sustainable pathway for China's coal-fired power plants, which could reduce air pollutant emissions, improve the energy efficiency, and slow down the construction of new units. However, continuous construction of new coal-fired power plants driven by increased electricity demand would pose a potential threat to climate change mitigation and China's peak carbon pledge, and more aggressive CO2 emission reduction policy should be implemented in the future.

40 CFR 75.30 - General provisions.

Code of Federal Regulations, 2012 CFR

2012-07-01

...) CONTINUOUS EMISSION MONITORING Missing Data Substitution Procedures § 75.30 General provisions. (a) Except as... continuous emission monitoring system according to the missing data procedures in this subpart whenever the... missing data procedures in this subpart if the owner or operator uses SO2, CO2, NOX, or O2 concentration...

40 CFR 75.31 - Initial missing data procedures.

Code of Federal Regulations, 2011 CFR

2011-07-01

... 40 Protection of Environment 16 2011-07-01 2011-07-01 false Initial missing data procedures. 75.31... (CONTINUED) CONTINUOUS EMISSION MONITORING Missing Data Substitution Procedures § 75.31 Initial missing data..., or O2 concentration data, and moisture data. For each hour of missing SO2 or CO2 emissions...

40 CFR 75.31 - Initial missing data procedures.

Code of Federal Regulations, 2013 CFR

2013-07-01

... 40 Protection of Environment 17 2013-07-01 2013-07-01 false Initial missing data procedures. 75.31... (CONTINUED) CONTINUOUS EMISSION MONITORING Missing Data Substitution Procedures § 75.31 Initial missing data..., or O2 concentration data, and moisture data. For each hour of missing SO2 or CO2 emissions...

40 CFR 75.30 - General provisions.

Code of Federal Regulations, 2011 CFR

2011-07-01

...) CONTINUOUS EMISSION MONITORING Missing Data Substitution Procedures § 75.30 General provisions. (a) Except as... continuous emission monitoring system according to the missing data procedures in this subpart whenever the... missing data procedures in this subpart if the owner or operator uses SO2, CO2, NOX, or O2 concentration...

40 CFR 75.31 - Initial missing data procedures.

Code of Federal Regulations, 2012 CFR

2012-07-01

... 40 Protection of Environment 17 2012-07-01 2012-07-01 false Initial missing data procedures. 75.31... (CONTINUED) CONTINUOUS EMISSION MONITORING Missing Data Substitution Procedures § 75.31 Initial missing data..., or O2 concentration data, and moisture data. For each hour of missing SO2 or CO2 emissions...

40 CFR 75.31 - Initial missing data procedures.

Code of Federal Regulations, 2014 CFR

2014-07-01

... 40 Protection of Environment 17 2014-07-01 2014-07-01 false Initial missing data procedures. 75.31... (CONTINUED) CONTINUOUS EMISSION MONITORING Missing Data Substitution Procedures § 75.31 Initial missing data..., or O2 concentration data, and moisture data. For each hour of missing SO2 or CO2 emissions...

40 CFR 75.30 - General provisions.

Code of Federal Regulations, 2013 CFR

2013-07-01

...) CONTINUOUS EMISSION MONITORING Missing Data Substitution Procedures § 75.30 General provisions. (a) Except as... continuous emission monitoring system according to the missing data procedures in this subpart whenever the... missing data procedures in this subpart if the owner or operator uses SO2, CO2, NOX, or O2 concentration...

40 CFR 75.30 - General provisions.

Code of Federal Regulations, 2010 CFR

2010-07-01

...) CONTINUOUS EMISSION MONITORING Missing Data Substitution Procedures § 75.30 General provisions. (a) Except as... continuous emission monitoring system according to the missing data procedures in this subpart whenever the... missing data procedures in this subpart if the owner or operator uses SO2, CO2, NOX, or O2 concentration...

40 CFR 75.30 - General provisions.

Code of Federal Regulations, 2014 CFR

2014-07-01

...) CONTINUOUS EMISSION MONITORING Missing Data Substitution Procedures § 75.30 General provisions. (a) Except as... continuous emission monitoring system according to the missing data procedures in this subpart whenever the... missing data procedures in this subpart if the owner or operator uses SO2, CO2, NOX, or O2 concentration...

Forcings and feedbacks by land ecosystem changes on climate change

NASA Astrophysics Data System (ADS)

Betts, R. A.

2006-12-01

Vegetation change is involved in climate change through both forcing and feedback processes. Emissions of CO{2} from past net deforestation are estimated to have contributed approximately 0.22 0.51 Wm - 2 to the overall 1.46 Wm - 2 radiative forcing by anthropogenic increases in CO{2} up to the year 2000. Deforestation-induced increases in global mean surface albedo are estimated to exert a radiative forcing of 0 to -0.2 Wm - 2, and dust emissions from land use may exert a radiative forcing of between approximately +0.1 and -0.2 Wm - 2. Changes in the fluxes of latent and sensible heat due to tropical deforestation are simulated to have exerted other local warming effects which cannot be quantified in terms of a Wm - 2 radiative forcing, with the potential for remote effects through changes in atmospheric circulation. With tropical deforestation continuing rapidly, radiative forcing by surface albedo change may become less useful as a measure of the forcing of climate change by changes in the physical properties of the land surface. Although net global deforestation is continuing, future scenarios used for climate change prediction suggest that fossil fuel emissions of CO{2} may continue to increase at a greater rate than land use emissions and therefore continue to increase in dominance as the main radiative forcing. The CO{2} rise may be accelerated by up to 66% by feedbacks arising from global soil carbon loss and forest dieback in Amazonia as a consequence of climate change, and Amazon forest dieback may also exert feedbacks through changes in the local water cycle and increases in dust emissions.

Greenhouse gases emissions accounting for typical sewage sludge digestion with energy utilization and residue land application in China.

PubMed

Niu, Dong-jie; Huang, Hui; Dai, Xiao-hu; Zhao, You-cai

2013-01-01

About 20 million tonnes of sludge (with 80% moisture content) is discharged by the sewage treatment plants per year in China, which, if not treated properly, can be a significant source of greenhouse gases (GHGs) emissions. Anaerobic digestion is a conventional sewage sludge treatment method and will continue to be one of the main technologies in the following years. This research has taken into consideration GHGs emissions from typical processes of sludge thickening+anaerobic digestion+dewatering+residue land application in China. Fossil CO(2), biogenic CO(2), CH(4,) and avoided CO(2) as the main objects is discussed respectively. The results show that the total CO(2)-eq is about 1133 kg/t DM (including the biogenic CO(2)), while the net CO(2)-eq is about 372 kg/t DM (excluding the biogenic CO(2)). An anaerobic digestion unit as the main GHGs emission source occupies more than 91% CO(2)-eq of the whole process. The use of biogas is important for achieving carbon dioxide emission reductions, which could reach about 24% of the total CO(2)-eq reduction. Copyright © 2012 Elsevier Ltd. All rights reserved.

Comparative study for hardwood and softwood forest biomass: chemical characterization, combustion phases and gas and particulate matter emissions.

PubMed

Amaral, Simone Simões; de Carvalho, João Andrade; Costa, Maria Angélica Martins; Soares Neto, Turíbio Gomes; Dellani, Rafael; Leite, Luiz Henrique Scavacini

2014-07-01

Two different types of typical Brazilian forest biomass were burned in the laboratory in order to compare their combustion characteristics and pollutant emissions. Approximately 2 kg of Amazon biomass (hardwood) and 2 kg of Araucaria biomass (softwood) were burned. Gaseous emissions of CO2, CO, and NOx and particulate matter smaller than 2.5 μm (PM2.5) were evaluated in the flaming and smoldering combustion phases. Temperature, burn rate, modified combustion efficiency, emissions factor, and particle diameter and concentration were studied. A continuous analyzer was used to quantify gas concentrations. A DataRam4 and a Cascade Impactor were used to sample PM2.5. Araucaria biomass (softwood) had a lignin content of 34.9%, higher than the 23.3% of the Amazon biomass (hardwood). CO2 and CO emissions factors seem to be influenced by lignin content. Maximum concentrations of CO2, NOx and PM2.5 were observed in the flaming phase. Copyright © 2014 Elsevier Ltd. All rights reserved.

Atmospheric inversion for cost effective quantification of city CO2 emissions

NASA Astrophysics Data System (ADS)

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

2015-11-01

Cities, currently covering only a very small portion (< 3 %) of the world's land surface, directly release to the atmosphere about 44 % of global energy-related CO2, and are associated with 71-76 % of CO2 emissions from global final energy use. Although many cities have set voluntary climate plans, their CO2 emissions are not evaluated by Monitoring, Reporting and Verification (MRV) procedures that play a key role for market- or policy-based mitigation actions. Here we propose a monitoring tool that could support the development of such procedures at the city scale. It is based on an atmospheric inversion method that exploits inventory data and continuous atmospheric CO2 concentration measurements from a network of stations within and around cities to estimate city CO2 emissions. We examine the cost-effectiveness and the performance of such a tool. The instruments presently used to measure CO2 concentrations at research stations are expensive. However, cheaper sensors are currently developed and should be useable for the monitoring of CO2 emissions from a megacity in the near-term. Our assessment of the inversion method is thus based on the use of several types of hypothetical networks, with a range of numbers of sensors sampling at 25 m a.g.l. The study case for this assessment is the monitoring of the emissions of the Paris metropolitan area (~ 12 million inhabitants and 11.4 Tg C emitted in 2010) during the month of January 2011. The performance of the inversion is evaluated in terms of uncertainties in the estimates of total and sectoral CO2 emissions. These uncertainties are compared to a notional ambitious target to diagnose annual total city emissions with an uncertainty of 5 % (2-sigma). We find that, with 10 stations only, which is the typical size of current pilot networks that are deployed in some cities, the uncertainty for the 1-month total city CO2 emissions is significantly reduced by the inversion by ~ 42 % but still corresponds to an annual uncertainty that is two times larger than the target of 5 %. By extending the network from 10 to 70 stations, the inversion can meet this requirement. As for major sectoral CO2 emissions, the uncertainties in the inverted emissions using 70 stations are reduced significantly over that obtained using 10 stations by 32 % for commercial and residential buildings, by 33 % for road transport and by 18 % for the production of energy by power plants, respectively. With 70 stations, the uncertainties from the inversion become of 15 % 2-sigma annual uncertainty for dispersed building emissions, and 18 % for emissions from road transport and energy production. The inversion performance could be further improved by optimal design of station locations and/or by assimilating additional atmospheric measurements of species that are co-emitted with CO2 by fossil fuel combustion processes with a specific signature from each sector, such as carbon monoxide (CO). Atmospheric inversions based on continuous CO2 measurements from a large number of cheap sensors can thus deliver a valuable quantification tool for the monitoring and/or the verification of city CO2 emissions (baseline) and CO2 emission reductions (commitments).

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

NASA Astrophysics Data System (ADS)

Tokarska, Katarzyna; Zickfeld, Kirsten

2014-05-01

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

Life Comparative Analysis of Energy Consumption and CO2 Emissions of Different Building Structural Frame Types

PubMed Central

Kim, Sangyong; Moon, Joon-Ho; Shin, Yoonseok; Kim, Gwang-Hee; Seo, Deok-Seok

2013-01-01

The objective of this research is to quantitatively measure and compare the environmental load and construction cost of different structural frame types. Construction cost also accounts for the costs of CO2 emissions of input materials. The choice of structural frame type is a major consideration in construction, as this element represents about 33% of total building construction costs. In this research, four constructed buildings were analyzed, with these having either reinforced concrete (RC) or steel (S) structures. An input-output framework analysis was used to measure energy consumption and CO2 emissions of input materials for each structural frame type. In addition, the CO2 emissions cost was measured using the trading price of CO2 emissions on the International Commodity Exchange. This research revealed that both energy consumption and CO2 emissions were, on average, 26% lower with the RC structure than with the S structure, and the construction costs (including the CO2 emissions cost) of the RC structure were about 9.8% lower, compared to the S structure. This research provides insights through which the construction industry will be able to respond to the carbon market, which is expected to continue to grow in the future. PMID:24227998

Dual-laser-beam-induced breakdown spectroscopy of copper using simultaneous continuous wave CO(2) and Q-switched Nd:YAG lasers.

PubMed

Shoursheini, S Z; Parvin, P; Sajad, B; Bassam, M A

2009-04-01

In this work, we investigate the enhancement of Cu emission lines of a micro-plasma induced by a Nd:YAG laser due to the thermal effect of simultaneous irradiation by a continuous wave (CW) CO(2) laser. The enhancement of the emission lines was achieved at a higher temperature with minimal distortion of the target when the focal point of the Nd:YAG laser was located approximately 1 mm away from the sample surface.

Towards Verifying National CO2 Emissions

NASA Astrophysics Data System (ADS)

Fung, I. Y.; Wuerth, S. M.; Anderson, J. L.

2017-12-01

With the Paris Agreement, nations around the world have pledged their voluntary reductions in future CO2 emissions. Satellite observations of atmospheric CO2 have the potential to verify self-reported emission statistics around the globe. We present a carbon-weather data assimilation system, wherein raw weather observations together with satellite observations of the mixing ratio of column CO2 from the Orbiting Carbon Observatory-2 are assimilated every 6 hours into the NCAR carbon-climate model CAM5 coupled to the Ensemble Kalman Filter of DART. In an OSSE, we reduced the fossil fuel emissions from a country, and estimated the emissions innovations demanded by the atmospheric CO2 observations. The uncertainties in the innovation are analyzed with respect to the uncertainties in the meteorology to determine the significance of the result. The work follows from "On the use of incomplete historical data to infer the present state of the atmosphere" (Charney et al. 1969), which maps the path for continuous data assimilation for weather forecasting and the five decades of progress since.

Year-round CH4 and CO2 flux dynamics in two contrasting freshwater ecosystems of the subarctic

NASA Astrophysics Data System (ADS)

Jammet, Mathilde; Dengel, Sigrid; Kettner, Ernesto; Parmentier, Frans-Jan W.; Wik, Martin; Crill, Patrick; Friborg, Thomas

2017-11-01

Lakes and wetlands, common ecosystems of the high northern latitudes, exchange large amounts of the climate-forcing gases methane (CH4) and carbon dioxide (CO2) with the atmosphere. The magnitudes of these fluxes and the processes driving them are still uncertain, particularly for subarctic and Arctic lakes where direct measurements of CH4 and CO2 emissions are often of low temporal resolution and are rarely sustained throughout the entire year. Using the eddy covariance method, we measured surface-atmosphere exchange of CH4 and CO2 during 2.5 years in a thawed fen and a shallow lake of a subarctic peatland complex. Gas exchange at the fen exhibited the expected seasonality of a subarctic wetland with maximum CH4 emissions and CO2 uptake in summer, as well as low but continuous emissions of CH4 and CO2 throughout the snow-covered winter. The seasonality of lake fluxes differed, with maximum CO2 and CH4 flux rates recorded at spring thaw. During the ice-free seasons, we could identify surface CH4 emissions as mostly ebullition events with a seasonal trend in the magnitude of the release, while a net CO2 flux indicated photosynthetic activity. We found correlations between surface CH4 emissions and surface sediment temperature, as well as between diel CO2 uptake and diel solar input. During spring, the breakdown of thermal stratification following ice thaw triggered the degassing of both CH4 and CO2. This spring burst was observed in 2 consecutive years for both gases, with a large inter-annual variability in the magnitude of the CH4 degassing. On the annual scale, spring emissions converted the lake from a small CO2 sink to a CO2 source: 80 % of total annual carbon emissions from the lake were emitted as CO2. The annual total carbon exchange per unit area was highest at the fen, which was an annual sink of carbon with respect to the atmosphere. Continuous respiration during the winter partly counteracted the fen summer sink by accounting for, as both CH4 and CO2, 33 % of annual carbon exchange. Our study shows (1) the importance of overturn periods (spring or fall) for the annual CH4 and CO2 emissions of northern lakes, (2) the significance of lakes as atmospheric carbon sources in subarctic landscapes while fens can be a strong carbon sink, and (3) the potential for ecosystem-scale eddy covariance measurements to improve the understanding of short-term processes driving lake-atmosphere exchange of CH4 and CO2.

40 CFR 75.35 - Missing data procedures for CO2.

Code of Federal Regulations, 2011 CFR

2011-07-01

... 40 Protection of Environment 16 2011-07-01 2011-07-01 false Missing data procedures for CO2. 75.35... (CONTINUED) CONTINUOUS EMISSION MONITORING Missing Data Substitution Procedures § 75.35 Missing data... the 720 quality-assured monitor operating hours preceding implementation of the standard missing data...

40 CFR 75.35 - Missing data procedures for CO2.

Code of Federal Regulations, 2010 CFR

2010-07-01

... 40 Protection of Environment 16 2010-07-01 2010-07-01 false Missing data procedures for CO2. 75.35... (CONTINUED) CONTINUOUS EMISSION MONITORING Missing Data Substitution Procedures § 75.35 Missing data... the 720 quality-assured monitor operating hours preceding implementation of the standard missing data...

40 CFR 75.35 - Missing data procedures for CO 2.

Code of Federal Regulations, 2013 CFR

2013-07-01

... 40 Protection of Environment 17 2013-07-01 2013-07-01 false Missing data procedures for CO 2. 75... (CONTINUED) CONTINUOUS EMISSION MONITORING Missing Data Substitution Procedures § 75.35 Missing data... the 720 quality-assured monitor operating hours preceding implementation of the standard missing data...

40 CFR 75.35 - Missing data procedures for CO2.

Code of Federal Regulations, 2012 CFR

2012-07-01

... 40 Protection of Environment 17 2012-07-01 2012-07-01 false Missing data procedures for CO2. 75.35... (CONTINUED) CONTINUOUS EMISSION MONITORING Missing Data Substitution Procedures § 75.35 Missing data... the 720 quality-assured monitor operating hours preceding implementation of the standard missing data...

40 CFR 75.35 - Missing data procedures for CO 2.

Code of Federal Regulations, 2014 CFR

2014-07-01

... 40 Protection of Environment 17 2014-07-01 2014-07-01 false Missing data procedures for CO 2. 75... (CONTINUED) CONTINUOUS EMISSION MONITORING Missing Data Substitution Procedures § 75.35 Missing data... the 720 quality-assured monitor operating hours preceding implementation of the standard missing data...

Diurnal variation of CO2, CH4, and N2O emission fluxes continuously monitored in-situ in three environmental habitats in a subtropical estuarine wetland.

PubMed

Yang, Wen-Bin; Yuan, Chung-Shin; Tong, Chuan; Yang, Pin; Yang, Lei; Huang, Bang-Qin

2017-06-15

Wetlands play a crucial role in modulating atmospheric concentrations of greenhouse gases (GHGs) such as carbon dioxide (CO 2 ), methane (CH 4 ), and nitrous oxide (N 2 O). The key factors controlling GHG emission from subtropical estuarine wetlands were investigated in this study, which continuously monitored the uptake/emission of GHGs (CO 2 , CH 4 , and N 2 O) by/from a subtropical estuarine wetland located in the Minjiang estuary in the coastal region of southeastern China. A self-designed floating chamber was used to collect air samples on-site at three environmental habitats (Phragmites australis marsh, mudflats, and river water). The CO 2 , CH 4 , and N 2 O concentrations were then measured using an automated nondispersive infrared analyzer. The magnitudes of the CO 2 and N 2 O emission fluxes at the three habitats were ordered as river water>P. australis>mudflats. P. australis emitted GHGs through photosynthesis and respiration processes. Emissions of CH 4 from P. australis and the mudflats were revealed to be slightly higher than those from the river water. The total GHG emission fluxes at the three environmental habitats were quite similar (4.68-4.78gm -2 h -1 ). However, when the total carbon dioxide equivalent fluxes (CO 2 -e) were considered, the river water was discovered to emit the most CO 2 -e compared with P. australis and the mudflats. Based on its potential to increase global warming, N 2 O was the main contributor to the total GHG emission, with that emitted from the river water being the most considerable. Tidal water carried onto the marsh had its own GHG content and thus has acted as a source or sink of GHGs. However, water quality had a large effect on GHG emissions from the river water whereas the tidal water height did not. Both high salinity and large amounts of sulfates in the wetlands explicitly inhibited the activity of CH 4 -producing bacteria, particularly at nighttime. Copyright © 2017 Elsevier Ltd. All rights reserved.

Greenhouse gases emissions accounting for typical sewage sludge digestion with energy utilization and residue land application in China

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

Niu Dongjie, E-mail: niudongjie@tongji.edu.cn; UNEP-Tongji Institute of Environment for Sustainable Development, 1239 Siping Road, Shanghai 200092; Huang Hui

2013-01-15

Highlights: Black-Right-Pointing-Pointer GHGs emissions from sludge digestion + residue land use in China were calculated. Black-Right-Pointing-Pointer The AD unit contributes more than 97% of total biogenic GHGs emissions. Black-Right-Pointing-Pointer AD with methane recovery is attractive for sludge GHGs emissions reduction. - Abstract: About 20 million tonnes of sludge (with 80% moisture content) is discharged by the sewage treatment plants per year in China, which, if not treated properly, can be a significant source of greenhouse gases (GHGs) emissions. Anaerobic digestion is a conventional sewage sludge treatment method and will continue to be one of the main technologies in the followingmore » years. This research has taken into consideration GHGs emissions from typical processes of sludge thickening + anaerobic digestion + dewatering + residue land application in China. Fossil CO{sub 2}, biogenic CO{sub 2}, CH{sub 4,} and avoided CO{sub 2} as the main objects is discussed respectively. The results show that the total CO{sub 2}-eq is about 1133 kg/t DM (including the biogenic CO{sub 2}), while the net CO{sub 2}-eq is about 372 kg/t DM (excluding the biogenic CO{sub 2}). An anaerobic digestion unit as the main GHGs emission source occupies more than 91% CO{sub 2}-eq of the whole process. The use of biogas is important for achieving carbon dioxide emission reductions, which could reach about 24% of the total CO{sub 2}-eq reduction.« less

Is rapid growth in Internet usage environmentally sustainable for Australia? An empirical investigation.

PubMed

Salahuddin, Mohammad; Alam, Khorshed; Ozturk, Ilhan

2016-03-01

This study estimates the short- and long-run effects of Internet usage and economic growth on carbon dioxide (CO2) emissions using annual time series macro data for Australia for the period 1985-2012. Autoregressive distributive lag (ARDL) bounds and Gregory-Hansen structural break cointegration tests are applied. ARDL estimates indicate no significant long-run relationship between Internet usage and CO2 emissions, which implies that the rapid growth in Internet usage is still not an environmental threat for Australia. The study further indicates that higher level of economic growth is associated with lower level of CO2 emissions; however, Internet usage and economic growth have no significant short-run relationship with CO2 emissions. Financial development has both short-run and long-run significant positive association with CO2 emissions. The findings offer support in favor of energy efficiency gains and a reduction in energy intensity in Australia. However, impulse response and variance decomposition analysis suggest that Internet usage, economic growth and financial development will continue to impact CO2 emissions in the future, and as such, this study recommends that in addition to the existing measures to combat CO2 emissions, Australia needs to exploit the potential of the Internet not only to reduce its own carbon footprint but also to utilize information and communication technology (ICT)-enabled emissions abatement potential to reduce emissions in various other sectors across the economy, such as, power, renewable energy especially in solar and wind energy, agriculture, transport and service.

Continuing global significance of emissions of Montreal Protocol-restricted halocarbons in the United States and Canada

NASA Astrophysics Data System (ADS)

Hurst, D. F.; Lin, J. C.; Romashkin, P. A.; Daube, B. C.; Gerbig, C.; Matross, D. M.; Wofsy, S. C.; Hall, B. D.; Elkins, J. W.

2006-08-01

Contemporary emissions of six restricted, ozone-depleting halocarbons, chlorofluorocarbon-11 (CFC-11, CCl3F), CFC-12 (CCl2F2), CFC-113 (CCl2FCClF2), methyl chloroform (CH3CCl3), carbon tetrachloride (CCl4), and Halon-1211 (CBrClF2), and two nonregulated trace gases, chloroform (CHCl3) and sulfur hexafluoride (SF6), are estimated for the United States and Canada. The estimates derive from 900 to 2900 in situ measurements of each of these gases within and above the planetary boundary layer over the United States and Canada as part of the 2003 CO2 Budget and Regional Airborne-North America (COBRA-NA) study. Air masses polluted by anthropogenic sources, identified by concurrently elevated levels of carbon monoxide (CO), SF6, and CHCl3, were sampled over a wide geographical range of these two countries. For each polluted air mass, we calculated emission ratios of halocarbons to CO and employed the Stochastic Time-Inverted Lagrangian Transport (STILT) model to determine the footprint associated with the air mass. Gridded CO emission estimates were then mapped onto the footprints and combined with measured emission ratios to generate footprint-weighted halocarbon flux estimates. We present statistically significant linear relationships between halocarbon fluxes (excluding CCl4) and footprint-weighted population densities, with slopes representative of per capita emission rates. These rates indicate that contemporary emissions of five restricted halocarbons (excluding CCl4) in the United States and Canada continue to account for significant fractions (7-40%) of global emissions.

Shallow tillage generates higher N2O emissions: results of continuous chamber-based measurement in a winter wheat field.

NASA Astrophysics Data System (ADS)

Broux, François; Lognoul, Margaux; Theodorakopoulos, Nicolas; Hiel, Marie-Pierre; Bodson, Bernard; Heinesch, Bernard; Aubinet, Marc

2017-04-01

Agriculture is one of the most important contributors to GHG emission, notably through fertilized croplands. Though, few publications have studied simultaneously and through continuous measurement the N2O and CO2 emissions in cultivated lands. We conducted this study to assess the effect of farming practices and climate on both N2O and CO2 emissions from a winter wheat crop. The experiment was held in an experimental field in the loamy region in Belgium from March 2016 till crop harvest in August 2016. The fluxes were measured on two nearby parcels in a winter wheat field with restitution of the residues from previous crop. For the past 8 years, one parcel was subjected to a shallow tillage (ST, 10 cm depth) and the other one to a conventional tillage (CT, 25 cm depth). On each parcel, the emissions are assessed with homemade automated closed chambers. Measurement continuity and good temporal resolution (one mean flux every 4 hours) of the system allowed a fine detection and quantification of the emission peaks which usually represent the major part of N2O fluxes. In addition to gas fluxes, soil water content and temperature were measured continuously. Soil samples were taken regularly to determine soil pH, soil organic carbon and nitrogen pools (total, NO3- and NH4+) and study microbial diversity and nitrification/denitrification gene expression. Unexpectedly, results showed N2O emissions twice as large in the ST parcel as in the CT parcel. On the contrary, less important CO2 emissions were observed under ST. Several emission peaks of N2O were observed during the measurement period. The peaks occurred after fertilization events and seemed to be triggered by an elevation of soil water content. Interesting links could be made between soil NH4-N and NO3-N pools and N2O emissions. Nitrification being the main process originating the fluxes was suggested on the one hand by the temporal evolution of nitrogen pools and N2O emissions and on the other hand by the relation between spatial variability of the emissions with the soil nitrate content. A comparison of the emissions between ST and CT and a discussion on peaks temporal dynamic, focusing on their intensity, duration and starting time will be presented.

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.

Frozen Cropland Soil in Northeast China as Source of N2O and CO2 Emissions

PubMed Central

Qiao, Yunfa; Han, Xiaozeng; Brancher Franco, Roberta

2014-01-01

Agricultural soils are important sources of atmospheric N2O and CO2. However, in boreal agro-ecosystems the contribution of the winter season to annual emissions of these gases has rarely been determined. In this study, soil N2O and CO2 fluxes were measured for 6 years in a corn-soybean-wheat rotation in northeast China to quantify the contribution of wintertime N2O and CO2 fluxes to annual emissions. The treatments were chemical fertilizer (NPK), chemical fertilizer plus composted pig manure (NPKOM), and control (Cont.). Mean soil N2O fluxes among all three treatments in the winter (November–March), when soil temperatures are below −7°C for extended periods, were 0.89–3.01 µg N m−2 h−1, and in between the growing season and winter (October and April), when freeze-thaw events occur, 1.73–5.48 µg N m−2 h−1. The cumulative N2O emissions were on average 0.27–1.39, 0.03–0.08 and 0.03–0.11 kg N2O–N ha−1 during the growing season, October and April, and winter, respectively. The average contributions of winter N2O efflux to annual emissions were 6.3–12.1%. In all three seasons, the highest N2O emissions occurred in NPKOM, while NPK and Cont. emissions were similar. Cumulative CO2 emissions were 2.73–4.94, 0.13–0.20 and 0.07–0.11 Mg CO2-C ha−1 during growing season, October and April, and winter, respectively. The contribution of winter CO2 to total annual emissions was 2.0–2.4%. Our results indicate that in boreal agricultural systems in northeast China, CO2 and N2O emissions continue throughout the winter. PMID:25536036

Contributions of past and present human generations to committed warming caused by carbon dioxide.

PubMed

Friedlingstein, Pierre; Solomon, Susan

2005-08-02

We developed a highly simplified approach to estimate the contributions of the past and present human generations to the increase of atmospheric CO(2) and associated global average temperature increases. For each human generation of adopted 25-year length, we use simplified emission test cases to estimate the committed warming passed to successive children, grandchildren, and later generations. We estimate that the last and the current generation contributed approximately two thirds of the present-day CO(2)-induced warming. Because of the long time scale required for removal of CO(2) from the atmosphere as well as the time delays characteristic of physical responses of the climate system, global mean temperatures are expected to increase by several tenths of a degree for at least the next 20 years even if CO(2) emissions were immediately cut to zero; that is, there is a commitment to additional CO(2)-induced warming even in the absence of emissions. If the rate of increase of CO(2) emissions were to continue up to 2025 and then were cut to zero, a temperature increase of approximately 1.3 degrees C compared to preindustrial conditions would still occur in 2100, whereas a constant-CO(2)-emissions scenario after 2025 would more than double the 2100 warming. These calculations illustrate the manner in which each generation inherits substantial climate change caused by CO(2) emissions that occurred previously, particularly those of their parents, and shows that current CO(2) emissions will contribute significantly to the climate change of future generations.

China's growing CO2 emissions--a race between increasing consumption and efficiency gains.

PubMed

Peters, Glen P; Weber, Christopher L; Guan, Dabo; Hubacek, Klaus

2007-09-01

China's rapidly growing economy and energy consumption are creating serious environmental problems on both local and global scales. Understanding the key drivers behind China's growing energy consumption and the associated CO2 emissions is critical for the development of global climate policies and provides insight into how other emerging economies may develop a low emissions future. Using recently released Chinese economic input-output data and structural decomposition analysis we analyze how changes in China's technology, economic structure, urbanization, and lifestyles affect CO2 emissions. We find that infrastructure construction and urban household consumption, both in turn driven by urbanization and lifestyle changes, have outpaced efficiency improvements in the growth of CO2 emissions. Net trade had a small effect on total emissions due to equal, but significant, growth in emissions from the production of exports and emissions avoided by imports. Technology and efficiency improvements have only partially offset consumption growth, but there remains considerable untapped potential to reduce emissions by improving both production and consumption systems. As China continues to rapidly develop there is an opportunity to further implement and extend policies, such as the Circular Economy, that will help China avoid the high emissions path taken by today's developed countries.

Structural change as a key component for agricultural non-CO2 mitigation efforts.

PubMed

Frank, Stefan; Beach, Robert; Havlík, Petr; Valin, Hugo; Herrero, Mario; Mosnier, Aline; Hasegawa, Tomoko; Creason, Jared; Ragnauth, Shaun; Obersteiner, Michael

2018-03-13

Agriculture is the single largest source of anthropogenic non-carbon dioxide (non-CO 2 ) emissions. Reaching the climate target of the Paris Agreement will require significant emission reductions across sectors by 2030 and continued efforts thereafter. Here we show that the economic potential of non-CO 2 emissions reductions from agriculture is up to four times as high as previously estimated. In fact, we find that agriculture could achieve already at a carbon price of 25 $/tCO 2 eq non-CO 2 reductions of around 1 GtCO 2 eq/year by 2030 mainly through the adoption of technical and structural mitigation options. At 100 $/tCO 2 eq agriculture could even provide non-CO 2 reductions of 2.6 GtCO 2 eq/year in 2050 including demand side efforts. Immediate action to favor the widespread adoption of technical options in developed countries together with productivity increases through structural changes in developing countries is needed to move agriculture on track with a 2 °C climate stabilization pathway.

Future CO2 Emissions and Climate Change from Existing Energy Infrastructure

NASA Astrophysics Data System (ADS)

Davis, S. J.; Caldeira, K.; Matthews, D.

2010-12-01

If current greenhouse gas (GHG) concentrations remain constant, the world would be committed to several centuries of increasing global mean temperatures and sea level rise. By contrast, near elimination of anthropogenic CO2 emissions would be required to produce diminishing GHG concentrations consistent with stabilization of mean temperatures. Yet long-lived energy and transportation infrastructure now operating can be expected to contribute substantial CO2 emissions over the next 50 years. Barring widespread retrofitting of existing power plants with carbon capture and storage (CCS) technologies or the early decommissioning of serviceable infrastructure, these “committed emissions” represent infrastructural inertia which may be the primary contributor to total future warming commitment. With respect to GHG emissions, infrastructural inertia may be thought of as having two important and overlapping components: (i) infrastructure that directly releases GHGs to the atmosphere, and (ii) infrastructure that contributes to the continued production of devices that emit GHGs to the atmosphere. For example, the interstate highway and refueling infrastructure in the United States facilitates continued production of gasoline-powered automobiles. Here, we focus only on the warming commitment from infrastructure that directly releases CO2 to the atmosphere. Essentially, we answer the question: What if no additional CO2-emitting devices (e.g., power plants, motor vehicles) were built, but all the existing CO2-emitting devices were allowed to live out their normal lifetimes? What CO2 levels and global mean temperatures would we attain? Of course, the actual lifetime of devices may be strongly influenced by economic and policy constraints. For instance, a ban on new CO2-emitting devices would create tremendous incentive to prolong the lifetime of existing devices. Thus, our scenarios are not realistic, but offer a means of gauging the threat of climate change from existing devices relative to those devices that have yet to be built. We developed scenarios of global CO2 emissions from the energy sector using datasets of power plants and motor vehicles worldwide, as well as estimates of fossil fuel emissions produced directly by industry, households, businesses, and other forms of transport. We estimated lifetimes and annual emissions of infrastructure from historical data. We projected changes in CO2 and temperature in response to our calculated emissions using an intermediate-complexity coupled climate-carbon model (UVic ESCM). We calculate cumulative future emissions of 496 (282 to 701) gigatonnes of CO2 from combustion of fossil fuels by existing infrastructure between 2010 and 2060, forcing mean warming of 1.3°C (1.1 to 1.4°C) above the preindustrial era and atmospheric concentrations of CO2 less than 430 parts per million (ppm). Because these conditions would likely avoid many key impacts of climate change, we conclude that sources of the most threatening emissions have yet to be built. However, CO2-emitting infrastructure will expand unless extraordinary efforts are undertaken to develop alternatives.

DEVELOPING AN INTEGRATED MANAGEMENT SYSTEM FOR URBAN AND ENERGY PLANNING TOWARDS A LOW-CARBON CITY

NASA Astrophysics Data System (ADS)

Maeda, Hideto; Nakakubo, Toyohiko; Tokai, Akihiro

In this study, we developed an integrated management model that supports local government to make a promising energy saving measure on a block-scale combined with urban planning. We applied the model to Osaka city and estimated CO2 emissions from the residential and commercial buildings to 2050. The urban renewal cases selected in this study included advanced multipole accumulation case, normal multipole accumulation case, and actual trend continuation case. The energy saving options introduced in each case included all-electric HP system, micro grid system, and we also set the option where the greater CO2 reduction one is selected in each block. The results showed that CO2 emission in 2050 would be reduced by 54.8-57.6% relative to the actual condition by introducing the new energy system in all cases. In addition, the amount of CO2 reduction in actual trend continuation case was highest. The major factor was that the effect of CO2 emission reductions by installing the solar power generation panel was higher than the effect by utilizing heated water mutually on the high-density blocks in terms of total urban buildings' energy consumption.

Representativeness analysis of CO_{2} profiles near a tall tower and from commercial airliner programs

NASA Astrophysics Data System (ADS)

Chen, Huilin; Katrynski, Krzysztof; Nedelec, Philippe; Machida, Toshinobu; Matsueda, Hidekazu; Sawa, Yousuke; Gerbig, Christoph

2010-05-01

Aircraft profiles for atmospheric trace gases have been collected using both rental aircraft and from commercial airliners. High-accuracy regular in situ CO2 measurements aboard rental aircraft over northeast Poland have been upgraded since August 2008. During each flight, two profiles are taken with a spatial separation of 20 kilometers. Until now, 74 profiles with continuous CO2 have been collected. Meanwhile, aircraft profiles for carbon monoxide (CO) have been made aboard commercial airliners within MOZAIC (Measurement of Ozone, water vapor, carbon monoxide and nitrogen oxides by AIrbus in-service airCraft) and for CO2 within CONTRAIL (Comprehensive Observation Network for TRace gases byAIrLiner) respectively. Starting from 2011, IAGOS-ERI (Integration of routine Aircraft measurements into a Global Observing System - European Research Infrastructure) will provide continuous CO2, CH4 and H2O measurements using instruments deployed aboard commercial airliners, with many profiles during take-off and landing over airports distributed all over the globe. These profiles contain not only vertical gradients but also regionally representative information. It is of importance to investigate how these profiles could be used for applications such as satellite validation and inverse modeling to retrieve surface-atmosphere exchange fluxes of greenhouse gases at regional to continental scales. Especially profiles from commercial airliners near major cities, which are potentially influenced by local fossil fuel emissions, need to be assessed with respect to their regional representativeness. We analyzed CO profiles over Frankfurt airport from the MOZAIC and CO2 profiles from CONTRAIL using STILT (the Stochastic Time Inverted Lagrangian Transport model) combined with a high resolution CO emission map in central Europe. Combining STILT footprints (maps of sensitivities to upstream surface fluxes) with high resolution emission inventories allows to attribute the contribution fossil fuel emissions to local vs. regional sources. In contrast, we analyzed CO2 profiles over northeast Poland in a similar way, where fossil fuel emissions are insignificant. The representativeness analysis provides information on under which circumstances such profiles can be used for potential applications, i.e. satellite validation and inverse modeling. The analysis suggests that a combined measurement of CO2 and CO significantly improves the usability of the regular profiles, where CO serves as the emission tracer.

A Modeling Framework for Inference of Surface Emissions Using Mobile Observations

NASA Astrophysics Data System (ADS)

Fasoli, B.; Mitchell, L.; Crosman, E.; Mendoza, D. L.; Lin, J. C.

2016-12-01

Our ability to quantify surface emissions depends on the precision of observations and the spatial density of measurement networks. Mobile measurement techniques offer a cost effective strategy for quantifying atmospheric conditions over space without requiring a dense network of in-situ sites. However, interpretation of these data and inversion of dispersed measurements to estimate surface emissions can be difficult. We introduce a framework using the Stochastic Time-Inverted Lagrangian Transport (STILT) model that assimilates both spatially resolved observations and an emissions inventory to better estimate surface fluxes. Salt Lake City is a unique laboratory for the study of urban carbon emissions. It is the only U.S. city that utilizes light-rail trains to continuously measure high frequency carbon dioxide (CO2) and methane (CH4); it is home to one of the longest and most spatially resolved high precision CO2 measurement networks (air.utah.edu); and it is one of four cities in the world for which the Hestia anthropogenic emissions inventory has been produced which characterizes CO2 emissions at the scale of individual buildings and roadways. Using these data and modeling resources, we evaluate spatially resolved CO2 measurements and transported CO2 emissions on hourly timescales at a dense spatial resolution across Salt Lake City.

Carbon dioxide emission tallies for 210 U.S. coal-fired power plants: a comparison of two accounting methods.

PubMed

Quick, Jeffrey C

2014-01-01

Annual CO2 emission tallies for 210 coal-fired power plants during 2009 were more accurately calculated from fuel consumption records reported by the US. Energy Information Administration (EIA) than measurements from Continuous Emissions Monitoring Systems (CEMS) reported by the US. Environmental Protection Agency. Results from these accounting methods for individual plants vary by +/- 10.8%. Although the differences systematically vary with the method used to certify flue-gas flow instruments in CEMS, additional sources of CEMS measurement error remain to be identified. Limitations of the EIA fuel consumption data are also discussed. Consideration of weighing, sample collection, laboratory analysis, emission factor, and stock adjustment errors showed that the minimum error for CO2 emissions calculated from the fuel consumption data ranged from +/- 1.3% to +/- 7.2% with a plant average of +/- 1.6%. This error might be reduced by 50% if the carbon content of coal delivered to U.S. power plants were reported. Potentially, this study might inform efforts to regulate CO2 emissions (such as CO2 performance standards or taxes) and more immediately, the U.S. Greenhouse Gas Reporting Rule where large coal-fired power plants currently use CEMS to measure CO2 emissions. Moreover, if, as suggested here, the flue-gas flow measurement limits the accuracy of CO2 emission tallies from CEMS, then the accuracy of other emission tallies from CEMS (such as SO2, NOx, and Hg) would be similarly affected. Consequently, improved flue gas flow measurements are needed to increase the reliability of emission measurements from CEMS.

Continuous atmospheric monitoring of the injected CO2 behavior over geological storage sites using flux stations: latest technologies and resources

NASA Astrophysics Data System (ADS)

Burba, George; Madsen, Rodney; Feese, Kristin

2014-05-01

Flux stations have been widely used to monitor emission rates of CO2 from various ecosystems for climate research for over 30 years [1]. The stations provide accurate and continuous measurements of CO2 emissions with high temporal resolution. Time scales range from 20 times per second for gas concentrations, to 15-minute, hourly, daily, and multi-year periods. The emissions are measured from the upwind area ranging from thousands of square meters to multiple square kilometers, depending on the measurement height. The stations can nearly instantaneously detect rapid changes in emissions due to weather events, as well as changes caused by variations in human-triggered events (pressure leaks, control releases, etc.). Stations can also detect any slow changes related to seasonal dynamics and human-triggered low-frequency processes (leakage diffusion, etc.). In the past, station configuration, data collection and processing were highly-customized, site-specific and greatly dependent on "school-of-thought" practiced by a particular research group. In the last 3-5 years, due to significant efforts of global and regional CO2 monitoring networks (e.g., FluxNet, Ameriflux, Carbo-Europe, ICOS, etc.) and technological developments, the flux station methodology became fairly standardized and processing protocols became quite uniform [1]. A majority of current stations compute CO2 emission rates using the eddy covariance method, one of the most direct and defensible micrometeorological techniques [1]. Presently, over 600 such flux stations are in operation in over 120 countries, using permanent and mobile towers or moving platforms (e.g., automobiles, helicopters, and airplanes). Atmospheric monitoring of emission rates using such stations is now recognized as an effective method in regulatory and industrial applications, including carbon storage [2-8]. Emerging projects utilize flux stations to continuously monitor large areas before and after the injections, to locate and quantify leakages from the subsurface, to improve storage efficiency, and for other storage characterizations [5-8]. In this presentation, the latest regulatory and methodological updates are provided regarding atmospheric monitoring of the injected CO2 behavior using flux stations. These include 2013 improvements in methodology, as well as the latest literature, including regulatory documents for using the method and step-by-step instructions on implementing it in the field. Updates also include 2013 development of a fully automated remote unattended flux station capable of processing data on-the-go to continuously output final CO2 emission rates in a similar manner as a standard weather station outputs weather parameters. References: [1] Burba G. Eddy Covariance Method for Scientific, Industrial, Agricultural and Regulatory Applications. LI-COR Biosciences; 2013. [2] International Energy Agency. Quantification techniques for CO2 leakage. IEA-GHG; 2012. [3] US Department of Energy. Best Practices for Monitoring, Verification, and Accounting of CO2 Stored in Deep Geologic Formations. US DOE; 2012. [4] Liu G. (Ed.). Greenhouse Gases: Capturing, Utilization and Reduction. Intech; 2012. [5] Finley R. et al. An Assessment of Geological Carbon Sequestration Options in the Illinois Basin - Phase III. DOE-MGSC; DE-FC26-05NT42588; 2012. [6] LI-COR Biosciences. Surface Monitoring for Geologic Carbon Sequestration. LI-COR, 980-11916, 2011. [7] Eggleston H., et al. (Eds). IPCC Guidelines for National Greenhouse Gas Inventories, IPCC NGGI P, WMO/UNEP; 2006-2011. [8] Burba G., Madsen R., Feese K. Eddy Covariance Method for CO2 Emission Measurements in CCUS Applications: Principles, Instrumentation and Software. Energy Procedia, 40C: 329-336; 2013.

Continuous multi-plot measurements of CO2, CH4, N2O and H2O in a managed boreal forest - The importance of accounting for all greenhouse gases

NASA Astrophysics Data System (ADS)

Vestin, P.; Mölder, M.; Sundqvist, E.; Båth, A.; Lehner, I.; Weslien, P.; Klemedtsson, L.; Lindroth, A.

2015-12-01

In order to assess the effects of different management practices on the exchange of greenhouse gases (GHG), it is desirable to perform repeated and parallel measurements on both experimental and control plots. Here we demonstrate how a system system combining eddy covariance and gradient techniques can be used to perform this assessment in a managed forest ecosystem.The net effects of clear-cutting and stump harvesting on GHG fluxes were studied at the ICOS site Norunda, Sweden. Micrometeorological measurements (i.e., flux-gradient measurements in 3 m tall towers) allowed for quantification of CO2, CH4 and H2O fluxes (from May 2010) as well as N2O and H2O fluxes (from June 2011) at two stump harvested plots and two control plots. There was one wetter and one drier plot of each treatment. Air was continuously sampled at two heights in the towers and gas concentrations were analyzed for CH4, CO2, H2O (LGR DLT-100, Los Gatos Research) and N2O, H2O (QCL Mini Monitor, Aerodyne Research). Friction velocities and sensible heat fluxes were measured by sonic anemometers (Gill Windmaster, Gill Instruments Ltd). Automatic chamber measurements (CO2, CH4, H2O) were carried out in the adjacent forest stand and at the clear-cut during 2010.Average CO2 emissions for the first year ranged between 14.4-20.2 ton CO2 ha-1 yr-1. The clear-cut became waterlogged after harvest and a comparison of flux-gradient data and chamber data (from the adjacent forest stand) indicated a switch from a weak CH4 sink to a significant source at all plots. The CH4 emissions ranged between 0.8-4.5 ton CO2-eq. ha-1 yr-1. N2O emissions ranged between 0.4-2.6 ton CO2-eq. ha-1 yr-1. Enhanced N2O emission on the drier stump harvested plot was the only clear treatment effect on GHG fluxes that was observed. Mean CH4 and N2O emissions for the first year of measurements amounted up to 29% and 20% of the mean annual CO2 emissions, respectively. This highlights the importance of including all GHGs when assessing the climate impacts of different forest management options. Our results show that continuous multi-plot measurements of the main GHGs are possible also at sites where GHG fluxes are low, at a reasonable cost and with reduced plot inter-comparison uncertainties.

The effect of urbanization and industrialization on carbon emissions in Turkey: evidence from ARDL bounds testing procedure.

PubMed

Pata, Ugur Korkut

2018-03-01

This paper examines the dynamic short- and long-term relationship between per capita GDP, per capita energy consumption, financial development, urbanization, industrialization, and per capita carbon dioxide (CO 2 ) emissions within the framework of the environmental Kuznets curve (EKC) hypothesis for Turkey covering the period from 1974 to 2013. According to the results of the autoregressive distributed lag bounds testing approach, an increase in per capita GDP, per capita energy consumption, financial development, urbanization, and industrialization has a positive effect on per capita CO 2 emissions in the long term, and also the variables other than urbanization increase per capita CO 2 emissions in the short term. In addition, the findings support the validity of the EKC hypothesis for Turkey in the short and long term. However, the turning points obtained from long-term regressions lie outside the sample period. Therefore, as the per capita GDP increases in Turkey, per capita CO 2 emissions continue to increase.

Diurnal and seasonal variations of greenhouse gas emissions from a naturally ventilated dairy barn in a cold region

NASA Astrophysics Data System (ADS)

Huang, Dandan; Guo, Huiqing

2018-01-01

Carbon dioxide (CO2), methane (CH4), and nitrous oxide (N2O) emissions were quantified for a naturally ventilated free-stall dairy barn in the Canadian Prairies climate through continuous measurements for a year from February 2015 to January 2016, with ventilation rate estimated by a CO2 mass balance method. The results were categorized into seasonal emission profiles with monthly data measured on a typical day, and diurnal profiles in cold (January), warm (July), and mild seasons (October) of all three gases. Seasonal CO2, CH4, and N2O concentrations greatly fluctuated within ranges of 593-2433 ppm, 15-152 ppm, and 0.32-0.40 ppm, respectively, with obviously higher concentrations in the cold season. Emission factors of the three gases were summarized: seasonal N2O emission varied between 0.5 and 10 μg s-1 AU-1 with lower emission in the cold season, while seasonal CO2 and CH4 emissions were within narrow ranges of 112-119 mg s-1 AU-1 and 2.5-3.5 mg s-1 AU-1. The result suggested a lower enteric CH4 emission for dairy cows than that estimated by Environment Canada (2014). Significant diurnal effects (P < 0.05) were observed for CH4 emissions in all seasons with higher emissions in the afternoons and evenings. The total greenhouse gas (GHG) emission, which was calculated by summing the three GHG in CO2 equivalent, was mainly contributed by CO2 and CH4 emissions and showed no significant seasonal variations (P > 0.05), but obvious diurnal variations in all seasons. In comparison with previous studies, it was found that the dairy barn in a cold region climate with smaller vent openings had relatively higher indoor CO2 and CH4 concentrations, but comparable CO2 and CH4 emissions to most previous studies. Besides, ventilation rate, temperature, and relative humidity all significantly affected the three gas concentrations with the outdoor temperature being the most relevant factor (P < 0.01); however, they showed less or no statistical relations to emissions.

Responses of Soil CO2 Emissions to Extreme Precipitation Regimes: a Simulation on Loess Soil in Semi-arid Regions

NASA Astrophysics Data System (ADS)

Wang, R.; Zhao, M.; Hu, Y.; Guo, S.

2016-12-01

Responses of soil CO2 emission to natural precipitation play an essential role in regulating regional C cycling. With more erratic precipitation regimes, mostly likely of more frequent heavy rainstorms, projected into the future, extreme precipitation would potentially affect local soil moisture, plant growth, microbial communities, and further soil CO2 emissions. However, responses of soil CO2 emissions to extreme precipitation have not yet been systematically investigated. Such performances could be of particular importance for rainfed arable soil in semi-arid regions where soil microbial respiration stress is highly sensitive to temporal distribution of natural precipitation.In this study, a simulated experiment was conducted on bare loess soil from the semi-arid Chinese Loess Plateau. Three precipitation regimes with total precipitation amounts of 150 mm, 300 mm and 600 mm were carried out to simulate the extremely dry, business as usual, and extremely wet summer. The three regimes were individually materialized by wetting soils in a series of sub-events (10 mm or 150 mm). Co2 emissions from surface soil were continuously measured in-situ for one month. The results show that: 1) Evident CO2 emission pulses were observed immediately after applying sub-events, and cumulative CO2 emissions from events of total amount of 600 mm were greater than that from 150 mm. 3) In particular, for the same total amount of 600 mm, wetting regimes by applying four times of 150 mm sub-events resulted in 20% less CO2 emissions than by applying 60 times of 10 mm sub-events. This is mostly because its harsh 150 mm storms introduced more over-wet soil microbial respiration stress days (moisture > 28%). As opposed, for the same total amount of 150 mm, CO2 emissions from wetting regimes by applying 15 times of 10 mm sub-events were 22% lower than by wetting at once with 150 mm water, probably because its deficiency of soil moisture resulted in more over-dry soil microbial respiration stress days (moisture < 15%). Overall, soil CO2 emissions not only responded to total precipitation amount, but was also sensitive to precipitation regimes. Such differentiated responses of CO2 emissions highlight the necessity to properly account for relative contributions from CO2 emissions when projecting global carbon cycling into future climate scenarios.

Feasibility of biodiesel production and CO2 emission reduction by Monoraphidium dybowskii LB50 under semi-continuous culture with open raceway ponds in the desert area.

PubMed

Yang, Haijian; He, Qiaoning; Hu, Chunxiang

2018-01-01

Compared with other general energy crops, microalgae are more compatible with desert conditions. In addition, microalgae cultivated in desert regions can be used to develop biodiesel. Therefore, screening oil-rich microalgae, and researching the algae growth, CO 2 fixation and oil yield in desert areas not only effectively utilize the idle desertification lands and other resources, but also reduce CO 2 emission. Monoraphidium dybowskii LB50 can be efficiently cultured in the desert area using light resources, and lipid yield can be effectively improved using two-stage induction and semi-continuous culture modes in open raceway ponds (ORPs). Lipid content (LC) and lipid productivity (LP) were increased by 20% under two-stage industrial salt induction, whereas biomass productivity (BP) increased by 80% to enhance LP under semi-continuous mode in 5 m 2 ORPs. After 3 years of operation, M. dybowskii LB50 was successfully and stably cultivated under semi-continuous mode for a month during five cycles of repeated culture in a 200 m 2 ORP in the desert area. This culture mode reduced the supply of the original species. The BP and CO 2 fixation rate were maintained at 18 and 33 g m -2  day -1 , respectively. Moreover, LC decreased only during the fifth cycle of repeated culture. Evaporation occurred at 0.9-1.8 L m -2  day -1 , which corresponded to 6.5-13% of evaporation loss rate. Semi-continuous and two-stage salt induction culture modes can reduce energy consumption and increase energy balance through the energy consumption analysis of life cycle. This study demonstrates the feasibility of combining biodiesel production and CO 2 fixation using microalgae grown as feedstock under culture modes with ORPs by using the resources in the desert area. The understanding of evaporation loss and the sustainability of semi-continuous culture render this approach practically viable. The novel strategy may be a promising alternative to existing technology for CO 2 emission reduction and biofuel production.

Kinetic Temperature and Carbon Dioxide from Broadband Infrared Limb Emission Measurements Taken from the TIMED/SABER Instrument

NASA Technical Reports Server (NTRS)

Mertens, Christopher J.; Russell III, James M.; Mlynczak, Martin G.; She, Chiao-Yao; Schmidlin, Francis J.; Goldberg, Richard A.; Lopez-Puertas, Manuel; Wintersteiner, Peter P.; Picard, Richard H.; Winick, Jeremy R.;

Relative importance of thermal versus carbon dioxide induced warming from fossil-fuel combustion

NASA Astrophysics Data System (ADS)

Zhang, X.; Caldeira, K.

2015-12-01

The Earth is heated both when reduced carbon is oxidized to carbon dioxide and when outgoing longwave radiation is trapped by carbon dioxide in the atmosphere (CO2 greenhouse effect). The purpose of this study is to improve our understanding of time scales and relative magnitudes of climate forcing increase over time from pulse, continuous, and historical CO2 and thermal emissions. To estimate the amount of global warming that would be produced by thermal and CO2 emissions from fossil fuel combustion, we calculate thermal emissions with thermal contents of fossil fuels and estimate CO2 emissions with emission factors from Intergovernmental Panel on Climate Change (IPCC) AR5. We then use a schematic climate model mimicking Coupled Model Intercomparison Project Phase 5 to investigate the climate forcing and the time-integrated climate forcing. We show that, considered globally, direct thermal forcing from fossil fuel combustion is about 1.71% the radiative forcing from CO2 that has accumulated in the atmosphere from past fossil fuel combustion. When a new power plant comes on line, the radiative forcing from the accumulation of released CO2 exceeds the thermal emissions from the power plant in less than half a year (and about 3 months for coal plants). Due to the long lifetime of CO2 in the atmosphere, CO2 radiative forcing greatly overwhelms direct thermal forcing on longer time scales. Ultimately, the cumulative radiative forcing from the CO2 exceeds the direct thermal forcing by a factor of ~100,000.

Physiological advantages of dwarfing in surviving extinctions in high-CO2 oceans

NASA Astrophysics Data System (ADS)

Garilli, Vittorio; Rodolfo-Metalpa, Riccardo; Scuderi, Danilo; Brusca, Lorenzo; Parrinello, Daniela; Rastrick, Samuel P. S.; Foggo, Andy; Twitchett, Richard J.; Hall-Spencer, Jason M.; Milazzo, Marco

2015-07-01

Excessive CO2 in the present-day ocean-atmosphere system is causing ocean acidification, and is likely to cause a severe biodiversity decline in the future, mirroring effects in many past mass extinctions. Fossil records demonstrate that organisms surviving such events were often smaller than those before, a phenomenon called the Lilliput effect. Here, we show that two gastropod species adapted to acidified seawater at shallow-water CO2 seeps were smaller than those found in normal pH conditions and had higher mass-specific energy consumption but significantly lower whole-animal metabolic energy demand. These physiological changes allowed the animals to maintain calcification and to partially repair shell dissolution. These observations of the long-term chronic effects of increased CO2 levels forewarn of changes we can expect in marine ecosystems as CO2 emissions continue to rise unchecked, and support the hypothesis that ocean acidification contributed to past extinction events. The ability to adapt through dwarfing can confer physiological advantages as the rate of CO2 emissions continues to increase.

40 CFR 91.328 - Measurement equipment accuracy/calibration frequency table.

Code of Federal Regulations, 2010 CFR

2010-07-01

... (CONTINUED) AIR PROGRAMS (CONTINUED) CONTROL OF EMISSIONS FROM MARINE SPARK-IGNITION ENGINES Emission Test... appendix A to this subpart are met. (f) Verify that all NDIR analyzers meet the water rejection ratio and the CO2 rejection ratio as specified in § 91.325. (g) Verify that the dynamometer test stand and power...

Can Producing Oil Store Carbon? Greenhouse Gas Footprint of CO2EOR, Offshore North Sea.

PubMed

Stewart, R Jamie; Haszeldine, R Stuart

2015-05-05

Carbon dioxide enhanced oil recovery (CO2EOR) is a proven and available technology used to produce incremental oil from depleted fields while permanently storing large tonnages of injected CO2. Although this technology has been used successfully onshore in North America and Europe, there are currently no CO2EOR projects in the United Kingdom. Here, we examine whether offshore CO2EOR can store more CO2 than onshore projects traditionally have and whether CO2 storage can offset additional emissions produced through offshore operations and incremental oil production. Using a high-level Life Cycle system approach, we find that the largest contribution to offshore emissions is from flaring or venting of reproduced CH4 and CO2. These can already be greatly reduced by regulation. If CO2 injection is continued after oil production has been optimized, then offshore CO2EOR has the potential to be carbon negative--even when emissions from refining, transport, and combustion of produced crude oil are included. The carbon intensity of oil produced can be just 0.056-0.062 tCO2e/bbl if flaring/venting is reduced by regulation. This compares against conventional Saudi oil 0.040 tCO2e/bbl or mined shale oil >0.300 tCO2e/bbl.

40 CFR 89.311 - Analyzer calibration frequency.

Code of Federal Regulations, 2010 CFR

2010-07-01

... (CONTINUED) CONTROL OF EMISSIONS FROM NEW AND IN-USE NONROAD COMPRESSION-IGNITION ENGINES Emission Test... rejection ratio and the CO2 rejection ratio as specified in § 89.318. (e) Verify that the dynamometer test...

Decadal changes in CH4 and CO2 emissions on the Alaskan North Slope

NASA Astrophysics Data System (ADS)

Sweeney, C.; Commane, R.; Wofsy, S.; Dlugokencky, E. J.; Karion, A.; Stone, R. S.; Chang, R.; Tans, P. P.; Wolter, S.

2016-12-01

Large changes in surface air temperature, sea ice cover and permafrost in the Arctic Boreal Ecosystems (ABE) are significantly impacting the critical ecosystem services and human societies that are dependent on the ABE. In order to predict the outcome of continued change in the climate system of the ABE, it is necessary to look at how past changes in climate have affected the ABE. We look at 30 years of CH4 and 42 years of CO2 observations from the NOAA Global Greenhouse Gas Reference Network site in Barrow, Alaska. By eliminating background trends and only looking at data collected when winds are blowing off the North Slope we find very little change in CH4 enhancements, but significant changes in the CO2 enhancements coming off the tundra. The bulk of both CO2 and CH4 emissions appear to be emitted well after the first snow fall on the North Slope. CO2 emissions are a strongly correlation with summer surface temperatures, while CH4 emissions appear insensitive to the large temperature changes that occurred over the measurement period. These results suggest that CO2, and not CH4 emissions, are a likely pathway for the degradation of permafrost carbon.

Ambient-temperature co-oxidation catalysts

NASA Technical Reports Server (NTRS)

Upchurch, Billy T.; Schryer, David R.; Brown, Kenneth G.; Kielin, Erik J.

1991-01-01

Oxidation catalysts which operate at ambient temperature were developed for the recombination of carbon monoxide (CO) and oxygen (O2) dissociation products which are formed during carbon dioxide (CO2) laser operation. Recombination of these products to regenerate CO2 allows continuous operation of CO2 lasers in a closed cycle mode. Development of these catalyst materials provides enabling technology for the operation of such lasers from space platforms or in ground based facilities without constant gas consumption required for continuous open cycle operation. Such catalysts also have other applications in various areas outside the laser community for removal of CO from other closed environments such as indoor air and as an ambient temperature catalytic converter for control of auto emissions.

Opportunities for Decarbonizing Existing U.S. Coal-Fired Power Plants via CO2 Capture, Utilization and Storage.

PubMed

Zhai, Haibo; Ou, Yang; Rubin, Edward S

2015-07-07

This study employs a power plant modeling tool to explore the feasibility of reducing unit-level emission rates of CO2 by 30% by retrofitting carbon capture, utilization, and storage (CCUS) to existing U.S. coal-fired electric generating units (EGUs). Our goal is to identify feasible EGUs and their key attributes. The results indicate that for about 60 gigawatts of the existing coal-fired capacity, the implementation of partial CO2 capture appears feasible, though its cost is highly dependent on the unit characteristics and fuel prices. Auxiliary gas-fired boilers can be employed to power a carbon capture process without significant increases in the cost of electricity generation. A complementary CO2 emission trading program can provide additional economic incentives for the deployment of CCS with 90% CO2 capture. Selling and utilizing the captured CO2 product for enhanced oil recovery can further accelerate CCUS deployment and also help reinforce a CO2 emission trading market. These efforts would allow existing coal-fired EGUs to continue to provide a significant share of the U.S. electricity demand.

40 CFR 98.163 - Calculating GHG emissions.

Code of Federal Regulations, 2014 CFR

2014-07-01

... (CONTINUED) MANDATORY GREENHOUSE GAS REPORTING Hydrogen Production § 98.163 Calculating GHG emissions. You must calculate and report the annual CO2 emissions from each hydrogen production process unit using the... associated with each fuel and feedstock used for hydrogen production by following paragraphs (b)(1) through...

40 CFR 98.163 - Calculating GHG emissions.

Code of Federal Regulations, 2011 CFR

2011-07-01

... (CONTINUED) MANDATORY GREENHOUSE GAS REPORTING Hydrogen Production § 98.163 Calculating GHG emissions. You must calculate and report the annual CO2 emissions from each hydrogen production process unit using the... associated with each fuel and feedstock used for hydrogen production by following paragraphs (b)(1) through...

40 CFR 98.163 - Calculating GHG emissions.

Code of Federal Regulations, 2013 CFR

2013-07-01

... (CONTINUED) MANDATORY GREENHOUSE GAS REPORTING Hydrogen Production § 98.163 Calculating GHG emissions. You must calculate and report the annual CO2 emissions from each hydrogen production process unit using the... associated with each fuel and feedstock used for hydrogen production by following paragraphs (b)(1) through...

40 CFR 98.163 - Calculating GHG emissions.

Code of Federal Regulations, 2012 CFR

2012-07-01

... (CONTINUED) MANDATORY GREENHOUSE GAS REPORTING Hydrogen Production § 98.163 Calculating GHG emissions. You must calculate and report the annual CO2 emissions from each hydrogen production process unit using the... associated with each fuel and feedstock used for hydrogen production by following paragraphs (b)(1) through...

A multi-scale approach to monitor urban carbon-dioxide emissions in the atmosphere over Vancouver, Canada

NASA Astrophysics Data System (ADS)

Christen, A.; Crawford, B.; Ketler, R.; Lee, J. K.; McKendry, I. G.; Nesic, Z.; Caitlin, S.

2015-12-01

Measurements of long-lived greenhouse gases in the urban atmosphere are potentially useful to constrain and validate urban emission inventories, or space-borne remote-sensing products. We summarize and compare three different approaches, operating at different scales, that directly or indirectly identify, attribute and quantify emissions (and uptake) of carbon dioxide (CO2) in urban environments. All three approaches are illustrated using in-situ measurements in the atmosphere in and over Vancouver, Canada. Mobile sensing may be a promising way to quantify and map CO2 mixing ratios at fine scales across heterogenous and complex urban environments. We developed a system for monitoring CO2 mixing ratios at street level using a network of mobile CO2 sensors deployable on vehicles and bikes. A total of 5 prototype sensors were built and simultaneously used in a measurement campaign across a range of urban land use types and densities within a short time frame (3 hours). The dataset is used to aid in fine scale emission mapping in combination with simultaneous tower-based flux measurements. Overall, calculated CO2 emissions are realistic when compared against a spatially disaggregated scale emission inventory. The second approach is based on mass flux measurements of CO2 using a tower-based eddy covariance (EC) system. We present a continuous 7-year long dataset of CO2 fluxes measured by EC at the 28m tall flux tower 'Vancouver-Sunset'. We show how this dataset can be combined with turbulent source area models to quantify and partition different emission processes at the neighborhood-scale. The long-term EC measurements are within 10% of a spatially disaggregated scale emission inventory. Thirdly, at the urban scale, we present a dataset of CO2 mixing ratios measured using a tethered balloon system in the urban boundary layer above Vancouver. Using a simple box model, net city-scale CO2 emissions can be determined using measured rate of change of CO2 mixing ratios, estimated CO2 advection and entrainment fluxes. Daily city-scale emissions totals predicted by the model are within 32% of a spatially scaled municipal greenhouse gas inventory. In summary, combining information from different approaches and scales is a promising approach to establish long-term emission monitoring networks in cities.

Stable carbon isotopes to monitor the CO2 source mix in the urban environment

NASA Astrophysics Data System (ADS)

Vogel, F. R.; Wu, L.; Ramonet, M.; Broquet, G.; Worthy, D. E. J.

2014-12-01

Urban areas are said to be responsible for approximately 71% of fossil fuel CO2 emissions while comprising only two percent of the land area [IEA, 2008]. This limited spatial expansion could facility a monitoring of anthropogenic GHGs from atmospheric observations. As major sources of emissions, cities also have a huge potential to drive emissions reductions. To effectively manage emissions, cities must however, first establish techniques to validate their reported emission statistics. A pilot study which includes continues 13CO2 data from calibrated cavity ring-down spectrometers [Vogel et al. 2013] of two "sister sites" in the vicinity of Toronto, Canada is contrasted to recent observations of 13CO2 observations in Paris during significant pollution events. Using Miller-Tans plots [Miller and Tans, 2003] for our multi-season observations reveals significant changes of the source signatures of night time CO2 emissions which reflect the importance of natural gas burning in Megacities (up to 80% of fossil fuel sources) and show-case the potential of future isotope studies to determine source sectors. Especially the winter data this approach seems suitable to determine the source contribution of different fuel types (natural gas, liquid fuels and coal) which can inform the interpretation of other Greenhouse Gases and air pollution levels.

Multi-Scale Science Framework for Attributing and Tracking Greenhouse Gas Fluxes at LANL's Four Corners New Mexico Test Bed

NASA Astrophysics Data System (ADS)

Costigan, K. R.; Dubey, M. K.; Chylek, P.; Love, S. P.; Henderson, B. G.; Flowers, B. A.; Reisner, J. M.; Rahn, T.; Quick, C. R.

2010-12-01

Agreements to limit greenhouse gas emissions require scientifically valid methods for monitoring and validating anthropogenic emissions. However, the task of monitoring CO2 emissions is difficult because relatively small increases need to be detected against CO2’s variable and large background concentrations. To ensure fair compliance, remotely sensed measurements and an understanding of the atmospheric transport of CO2 from the sources are required. We hypothesize that CO2 from various natural and anthropogenic sources can be distinguished and tracked by monitoring co-emitted gases (e.g. NO2, SO2, and CO) and isotopomers (e.g.13CO2). The ratio of a co-emitted species to CO2 depends on fuel composition and combustion process and thus varies by energy sector. These ratios provide an independent method to quantify CO2 emissions. Their low backgrounds, their large perturbations from energy activities, and our ability to measure them precisely make them sensitive probes to attribute sources, especially when emission ratios of multiple species are used concurrently. This strategy of observing emission ratios of co-emitted species to derive regional and source-specific baselines and CO2 fluxes is being tested in the Four Corners region of northwestern New Mexico. The semi-arid ecology in the region has a weak natural carbon cycle, facilitating our goal of dissection of anthropogenic sector-specific sources. The net Four Corners and San Juan power plant emissions are the largest point source of CO2 and NOx in North America. The Four Corners plant produces much more NOx than the San Juan power plant, while their energy and CO2 outputs, and coal used, are similar. This difference offers us a unique opportunity to test discrimination methods. While their CO2 signals remain elusive for current satellites, their NO2 plumes have recently been resolved from space. The region also experiences dispersed CO2 urban emissions as well as emissions and leaks from thousands of oil/gas wells. All of this makes the site an ideal test-bed. Our approach is to execute a systematic and coordinated observational, satellite validation and modeling program. We are instrumenting the Four Corners ground site with an array of state-of-the art, in situ and remote sensors, including LANL’s solar FTS and in situ sensors for continuous long term monitoring. Satellite measurements are also analyzed and have revealed that recent environmental upgrades have reduced NOx emissions, verifying bottom up inventories. A coordinated field campaign is planned, which will interrogate the power plant plume and regional dynamics and chemistry. Modeling using the plants’ reported emissions will be compared with observations to test the veracity of our approach. Early modeling, satellite analyses and measurements will be presented.

40 CFR 98.193 - Calculating GHG emissions.

Code of Federal Regulations, 2010 CFR

2010-07-01

... (CONTINUED) MANDATORY GREENHOUSE GAS REPORTING Lime Manufacturing § 98.193 Calculating GHG emissions. You must calculate and report the annual process CO2 emissions from all lime kilns combined using the procedure in paragraphs (a) and (b) of this section. (a) If all lime kilns meet the conditions specified in...

SEASONAL COURSE OF ISOPRENE EMISSIONS FROM A MIDLATITUDE DECIDUOUS FOREST

EPA Science Inventory

Continuous measurements of whole canopy isoprene emissions over an entire growing season are reported from Harvard Forest (42E32'N, 72E11'W). Emissions were calculated from the ratio of observed CO2 flux and gradient multiplied by the observed hydrocarbon gradients. In summer 199...

Unconsidered sporadic sources of carbon dioxide emission from soils in taiga forests.

PubMed

Karelin, D V; Zamolodchikov, D G; Isaev, A S

2017-07-01

Long-term monitoring in the Russian taiga zone has shown that all known extreme destructive effects resulting in the weakening and death of tree stands (windfalls, pest attacks, drought events, etc.) can be sporadic, but significant sources of CO 2 soil emission. Among them are (i) a recently found effect of the multiyear CO 2 emission from soil at the bottom of deadwood of spruce trees that died due to climate warming and subsequent pest outbreaks, (ii) increased soil CO 2 emissions due to to the fall of tree trunks during massive windfalls, and (iii) pulse CO 2 emission as a result of the so-called Birch effect after drought events in the taiga zone. According to the modeling, while depending on the spatial and temporal scales of their manifestation, the impact of these sporadic effects on the regional and global soil respiration fluxes could be significant and should be taken into consideration. This is due to continuing Climate Change, and further increase of local, regional and Global human impacts on the atmospheric greenhouse gases balance, and land use, as well.

Low-cost, high-density sensor network for urban emission monitoring: BEACO2N

NASA Astrophysics Data System (ADS)

Kim, J.; Shusterman, A.; Lieschke, K.; Newman, C.; Cohen, R. C.

2017-12-01

In urban environments, air quality is spatially and temporally heterogeneous as diverse emission sources create a high degree of variability even at the neighborhood scale. Conventional air quality monitoring relies on continuous measurements with limited spatial resolution or passive sampling with high-density and low temporal resolution. Either approach averages the air quality information over space or time and hinders our attempts to understand emissions, chemistry, and human exposure in the near-field of emission sources. To better capture the true spatio-temporal heterogeneity of urban conditions, we have deployed a low-cost, high-density air quality monitoring network in San Francisco Bay Area distributed at 2km horizontal spacing. The BErkeley Atmospheric CO2 Observation Network (BEACO2N) consists of approximately 50 sensor nodes, measuring CO2, CO, NO, NO2, O­3, and aerosol. Here we describe field-based calibration approaches that are consistent with the low-cost strategy of the monitoring network. Observations that allow inference of emission factors and identification of specific local emission sources will also be presented.

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

NASA Astrophysics Data System (ADS)

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

2016-05-01

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

40 CFR 86.320-79 - Analyzer bench check.

Code of Federal Regulations, 2010 CFR

2010-07-01

... (CONTINUED) CONTROL OF EMISSIONS FROM NEW AND IN-USE HIGHWAY VEHICLES AND ENGINES Emission Regulations for...) Water rejection ratio, NDIR analyzers only (see §§ 86.316(c) and 86.318 (b)(5). (7) CO2 rejection ratio...

Monitoring CO2 emissions to gain a dynamic view of carbon allocation to arbuscular mycorrhizal fungi.

PubMed

Slavíková, Renata; Püschel, David; Janoušková, Martina; Hujslová, Martina; Konvalinková, Tereza; Gryndlerová, Hana; Gryndler, Milan; Weiser, Martin; Jansa, Jan

2017-01-01

Quantification of carbon (C) fluxes in mycorrhizal plants is one of the important yet little explored tasks of mycorrhizal physiology and ecology. 13 CO 2 pulse-chase labelling experiments are increasingly being used to track the fate of C in these plant-microbial symbioses. Nevertheless, continuous monitoring of both the below- and aboveground CO 2 emissions remains a challenge, although it is necessary to establish the full C budget of mycorrhizal plants. Here, a novel CO 2 collection system is presented which allows assessment of gaseous CO 2 emissions (including isotopic composition of their C) from both belowground and shoot compartments. This system then is used to quantify the allocation of recently fixed C in mycorrhizal versus nonmycorrhizal Medicago truncatula plants with comparable biomass and mineral nutrition. Using this system, we confirmed substantially greater belowground C drain in mycorrhizal versus nonmycorrhizal plants, with the belowground CO 2 emissions showing large variation because of fluctuating environmental conditions in the glasshouse. Based on the assembled 13 C budget, the C allocation to the mycorrhizal fungus was between 2.3% (increased 13 C allocation to mycorrhizal substrate) and 2.9% (reduction of 13 C allocation to mycorrhizal shoots) of the plant gross photosynthetic production. Although the C allocation to shoot respiration (measured during one night only) did not differ between the mycorrhizal and nonmycorrhizal plants under our experimental conditions, it presented a substantial part (∼10%) of the plant C budget, comparable to the amount of CO 2 released belowground. These results advocate quantification of both above- and belowground CO 2 emissions in future studies.

40 CFR 60.84 - Emission monitoring.

Code of Federal Regulations, 2011 CFR

2011-07-01

... velocities or production rate. Continuous emission monitoring systems for measuring SO2, O2, and CO2 (if... H2SO4 produced. Cs=concentration of SO2, kg/dscm (lb/dscf). S=acid production rate factor, 368 dscm.... A=auxiliary fuel factor, =0.00 for no fuel. =0.0226 for methane. =0.0217 for natural gas. =0.0196...

40 CFR 60.84 - Emission monitoring.

Code of Federal Regulations, 2013 CFR

2013-07-01

... velocities or production rate. Continuous emission monitoring systems for measuring SO2, O2, and CO2 (if... H2SO4 produced. Cs=concentration of SO2, kg/dscm (lb/dscf). S=acid production rate factor, 368 dscm.... A=auxiliary fuel factor, =0.00 for no fuel. =0.0226 for methane. =0.0217 for natural gas. =0.0196...

40 CFR 60.84 - Emission monitoring.

Code of Federal Regulations, 2010 CFR

2010-07-01

... velocities or production rate. Continuous emission monitoring systems for measuring SO2, O2, and CO2 (if... H2SO4 produced. Cs=concentration of SO2, kg/dscm (lb/dscf). S=acid production rate factor, 368 dscm.... A=auxiliary fuel factor, =0.00 for no fuel. =0.0226 for methane. =0.0217 for natural gas. =0.0196...

40 CFR 60.84 - Emission monitoring.

Code of Federal Regulations, 2012 CFR

2012-07-01

... velocities or production rate. Continuous emission monitoring systems for measuring SO2, O2, and CO2 (if... H2SO4 produced. Cs=concentration of SO2, kg/dscm (lb/dscf). S=acid production rate factor, 368 dscm.... A=auxiliary fuel factor, =0.00 for no fuel. =0.0226 for methane. =0.0217 for natural gas. =0.0196...

40 CFR 60.84 - Emission monitoring.

Code of Federal Regulations, 2014 CFR

2014-07-01

... velocities or production rate. Continuous emission monitoring systems for measuring SO2, O2, and CO2 (if... of H2SO4 produced. Cs = concentration of SO2, kg/dscm (lb/dscf). S = acid production rate factor, 368... dry basis. A = auxiliary fuel factor, = 0.00 for no fuel. = 0.0226 for methane. = 0.0217 for natural...

40 CFR Table Nn-1 to Subpart Nn of... - Default Factors for Calculation Methodology 1 of This Subpart

Code of Federal Regulations, 2014 CFR

2014-07-01

... PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) MANDATORY GREENHOUSE GAS REPORTING Suppliers of Natural Gas and Natural Gas Liquids Pt. 98, Subpt. NN, Table NN-1 Table NN-1 to Subpart NN of Part 98... CO2emission factor (kg CO2/MMBtu) Natural Gas 1.026 MMBtu/Mscf 53.06 Propane 3.84 MMBtu/bbl 62.87 Normal...

Growth dynamics of carbon-metal particles and nanotubes synthesized by CO2 laser vaporization

NASA Astrophysics Data System (ADS)

Kokai, F.; Takahashi, K.; Yudasaka, M.; Iijima, S.

To study the growth of carbon-Co/Ni particles and single-wall carbon nanotubes (SWNTs) by 20 ms CO2 laser-pulse irradiation of a graphite-Co/Ni (1.2 at.%) target in an Ar gas atmosphere (600 Torr), we used emission imaging spectroscopy and shadowgraphy with a temporal resolution of 1.67 ms. Wavelength-selected emission images showed that C2 emission was strong in the region close to the target (within 2 cm), while for the same region the blackbody radiation from the large clusters or particles increased with increasing distance from the target. Shadowgraph images showed that the viscous flow of carbon and metal species formed a mushroom or a turbulent cloud spreading slowly into the Ar atmosphere, indicating that particles and SWNTs continued to grow as the ejected material cooled. In addition, emission imaging spectroscopy at 1200 °C showed that C2 and hot clusters and particles with higher emission intensities were distributed over much wider areas. We discuss the growth dynamics of the particles and SWNTs through the interaction of the ambient Ar with the carbon and metal species released from the target by the laser pulse.

CaO-based CO2 sorbents: from fundamentals to the development of new, highly effective materials.

PubMed

Kierzkowska, Agnieszka M; Pacciani, Roberta; Müller, Christoph R

2013-07-01

The enormous anthropogenic emission of the greenhouse gas CO2 is most likely the main reason for climate change. Considering the continuing and indeed growing utilisation of fossil fuels for electricity generation and transportation purposes, development and implementation of processes that avoid the associated emissions of CO2 are urgently needed. CO2 capture and storage, commonly termed CCS, would be a possible mid-term solution to reduce the emissions of CO2 into the atmosphere. However, the costs associated with the currently available CO2 capture technology, that is, amine scrubbing, are prohibitively high, thus making the development of new CO2 sorbents a highly important research challenge. Indeed, CaO, readily obtained through the calcination of naturally occurring limestone, has been proposed as an alternative CO2 sorbent that could substantially reduce the costs of CO2 capture. However, one of the major drawbacks of using CaO derived from natural sources is its rapidly decreasing CO2 uptake capacity with repeated carbonation-calcination reactions. Here, we review the current understanding of fundamental aspects of the cyclic carbonation-calcination reactions of CaO such as its reversibility and kinetics. Subsequently, recent attempts to develop synthetic, CaO-based sorbents that possess high and cyclically stable CO2 uptakes are presented. Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Spatial and Temporal Variations in the Partial Pressure and Emission of CO2 and CH4 in and Amazon Floodplain Lake

NASA Astrophysics Data System (ADS)

Forsberg, B. R.; Amaral, J. H.; Barbosa, P.; Kasper, D.; MacIntyre, S.; Cortes, A.; Sarmento, H.; Borges, A. V.; Melack, J. M.; Farjalla, V.

2015-12-01

The Amazon floodplain contains a variety of wetland environments which contribute CO2 and CH4 to the regional and global atmospheres. The partial pressure and emission of these greenhouse gases (GHGs) varies: 1) between habitats, 2) seasonally, as the characteristics these habitats changes and 3) diurnally, in response to diurnal stratification. In this study, we investigated the combined influence of these factors on the partial pressure and emission of GHGs in Lago Janauacá, a central Amazon floodplain lake (3o23' S; 60o18' O). All measurements were made between August of 2014 and April of 2015 at two different sites and in three distinct habitats: open water, flooded forest, flooded macrophytes. Concentrations of CO2 and CH4 in air were measured continuously with a cavity enhanced absorption spectrometer, Los Gatos Research´s Ultraportable Greenhouse Gas Analyzer (UGGA). Vertical profiles o pCO2 and pCH4 were measured using the UGGA connected to an electric pump and equilibrator. Diffusive surface emissions were estimated with the UGGA connected to a static floating chamber. To investigate the influence of vertical stratification and mixing on GHG partial pressure and emissions, a meteorological station and submersible sensor chain were deployed at each site. Meteorological sensors included wind speed and direction. The submersible chains included thermistors and oxygen sensors. Depth profiles of partial pressure and diffusive emissions for both CO2 and CH4 varied diurnally, seasonally and between habitats. Both pCO2 and pCH4 were consistently higher in bottom than surface waters with the largest differences occurring at high water when thermal stratification was most stable. Methane emissions and partial pressures were highest at low water while pCO2 and CO2 fluxes were highest during high water periods, with 35% of CO2 fluxes at low water being negative. The highest average surface value of pCO2 (5491 μatm), encountered during rising water, was ~3 times higher than that encountered at low water (1708 μatm). Partial pressures and emissions of both CO2 and CH4 were greatest in open water habitats and consistently higher at night. These patterns reflected the higher levels of wind driven mixing and turbulence in open water environments and higher convective mixing at night which promoted diffusive emission.

On-road and laboratory emissions of NO, NO2, NH3, N2O and CH4 from late-model EU light utility vehicles: Comparison of diesel and CNG.

PubMed

Vojtíšek-Lom, Michal; Beránek, Vít; Klír, Vojtěch; Jindra, Petr; Pechout, Martin; Voříšek, Tomáš

2018-03-01

Exhaust emissions of eight Euro 6 light duty vehicles - two station wagons and six vans - half powered by diesel fuel and half by compressed natural gas (CNG) were examined using both chassis dynamometer and on-road testing. A portable on-board FTIR analyzer was used to measure concentrations of reactive nitrogen compounds - NO, NO 2 and ammonia, of CO, formaldehyde, acetaldehyde and greenhouse gases CO 2 , methane and N 2 O. Exhaust flow was inferred from engine control unit data. Total emissions per cycle were compared and found to be in good agreement with laboratory measurements of NO X , CO and CO 2 during dynamometer tests. On diesel engines, mean NO X emissions were 136-1070mg/km in the laboratory and 537-615mg/km on the road, in many cases nearly an order of magnitude higher compared to the numerical value of the Euro 6 limit. Mean N 2 O emissions were 3-19mg/km and were equivalent to several g/km CO 2 . The measurements suggest that NO X and N 2 O emissions from late-model European light utility vehicles with diesel engines are non-negligible and should be continuously assessed and scrutinized. High variances in NO X emissions among the tested diesel vehicles suggest that large number of vehicles should be tested to offer at least some insights about distribution of fleet emissions among vehicles. CNG engines exhibited relatively low emissions of NO X (12-186mg/km) and NH 3 (10-24mg/km), while mean emissions of methane were 18-45mg/km, under 1g/km CO 2 equivalent, and N 2 O, CO, formaldehyde and acetaldehyde were negligible. The combination of a relatively clean-burning fuel, modern engine technology and a three-way catalyst has resulted in relatively low emissions under the wide variety of operating conditions encountered during the tests. The on-board FTIR has proven to be a useful instrument capable of covering, with the exception of total hydrocarbons, essentially all gaseous pollutants of interest. Copyright © 2017 Elsevier B.V. All rights reserved.

Measurements of Carbon Dioxide in the Portland, Oregon Metropolitan Region

NASA Astrophysics Data System (ADS)

Bostrom, G. A.; Rice, A. L.

2009-12-01

Urban centers provide large sources of carbon dioxide (CO2) to the atmosphere through intensive use of fossil fuels. Due to a lack of federal regulatory framework in the United States, a patchwork of regional and statewide approaches to reducing CO2 emissions has emerged. The City of Portland together with Multnomah County established itself as an early frontier in this regard by creating greenhouse gas emissions inventories in 1990 and adopting a regional plan to reduce emissions in 1993. Most recent emissions inventories suggest that County-wide emissions of CO2 are near 1990 levels, despite a growing population, with an ambitious goal of reducing emissions 80% by 2050. However, there has been no validation of either emissions inventories or their trends in time. Here, we detail preliminary results of a study aimed at testing regional CO2 emissions inventories through measurements of CO2 concentrations and its 13C isotopic composition. In collaboration with Oregon Department of Environmental Quality three test sites were established: a downtown Portland location on the campus of Portland State University; a residential Southeast Portland location; and at Sauvie Island, located ~30km northwest (upwind, rural) of Portland in the Columbia River Gorge. Continuous measurements of summertime CO2 concentrations since late July, 2009 range from approximately 370ppm to 420ppm (±2.7σ) for downtown and residential sites, and 360ppm to 420ppm for Sauvie Island, while maximum outlier levels at all three sites exceed 480ppm. Measurements at all three sites show a marked diurnal cycle averaging 25-35ppm. Maximum CO2 concentrations typically occur 6-8 am and minimum concentrations 5-7 pm. The two dominant forcing mechanisms of this strong diurnal cycle are varying biological sources and sinks and the dynamics of the planetary boundary layer. There is also a significant enhancement of ~7ppm in the average measured concentrations at the two urban sites (~395ppm) compared with the upwind Sauvie Island site (~388ppm). We interpret these results in terms of CO2 emissions inventories and sinks of CO2 in the Portland region. We also present preliminary measurements of the 13C isotopic composition of CO2 as a means of source apportionment with which to better refine emissions inventories.

Holocene peatland and ice-core data constraints on the timing and magnitude of CO2 emissions from past land use

PubMed Central

Massa, Charly

2017-01-01

CO2 emissions from preindustrial land-use change (LUC) are subject to large uncertainties. Although atmospheric CO2 records suggest only a small land carbon (C) source since 5,000 y before present (5 kyBP), the concurrent C sink by peat buildup could mask large early LUC emissions. Here, we combine updated continuous peat C reconstructions with the land C balance inferred from double deconvolution analyses of atmospheric CO2 and δ13C at different temporal scales to investigate the terrestrial C budget of the Holocene and the last millennium and constrain LUC emissions. LUC emissions are estimated with transient model simulations for diverging published scenarios of LU area change and shifting cultivation. Our results reveal a large terrestrial nonpeatland C source after the Mid-Holocene (66 ± 25 PgC at 7–5 kyBP and 115 ± 27 PgC at 5–3 kyBP). Despite high simulated per-capita CO2 emissions from LUC in early phases of agricultural development, humans emerge as a driver with dominant global C cycle impacts only in the most recent three millennia. Sole anthropogenic causes for particular variations in the CO2 record (∼20 ppm rise after 7 kyBP and ∼10 ppm fall between 1500 CE and 1600 CE) are not supported. This analysis puts a strong constraint on preindustrial vs. industrial-era LUC emissions and suggests that upper-end scenarios for the extent of agricultural expansion before 1850 CE are not compatible with the C budget thereafter. PMID:28137849

Spatial and temporal variations of diffuse CO2 degassing at El Hierro volcanic system: Relation to the 2011-2012 submarine eruption

NASA Astrophysics Data System (ADS)

Melián, Gladys; Hernández, Pedro A.; Padrón, Eleazar; Pérez, Nemesio M.; Barrancos, José; Padilla, Germán.; Dionis, Samara; Rodríguez, Fátima; Calvo, David; Nolasco, Dacil

2014-09-01

We report herein the results of extensive diffuse CO2 emission surveys performed on El Hierro Island in the period 1998-2012. More than 17,000 measurements of the diffuse CO2 efflux were carried out, most of them during the volcanic unrest period that started in July 2011. Two significant precursory signals based on geochemical and geodetical studies suggest that a magma intrusion processes might have started before 2011 in El Hierro Island. During the preeruptive and eruptive periods, the time series of the diffuse CO2 emission released by the whole island experienced two significant increases. The first started almost 2 weeks before the onset of the submarine eruption, reflecting a clear geochemical anomaly in CO2 emission, most likely due to increasing release of deep-seated magmatic gases to the surface. The second one, between 24 October and 27 November 2011, started before the most energetic seismic events of the volcanic-seismic unrest. The data presented here demonstrate that combined continuous monitoring studies and discrete surveys of diffuse CO2 emission provide important information to optimize the early warning system in volcano monitoring programs and to monitor the evolution of an ongoing volcanic eruption, even though it is a submarine eruption.

Effects of a clear-cut harvest on soil respiration in a jack pine - Lichen woodland

USGS Publications Warehouse

Striegl, Robert G.; Wickland, K.P.

1998-01-01

Quantification of the components of ecosystem respiration is essential to understanding carbon (C) cycling of natural and disturbed landscapes. Soil respiration, which includes autotrophic and heterotrophic respiration from throughout the soil profile, is the second largest flux in the global carbon cycle. We measured soil respiration (soil CO2 emission) at an undisturbed mature jack pine (Pinus banksiana Lamb.) stand in Saskatchewan (old jack pine, OJP), and at a formerly continuous portion of the stand that was clear-cut during the previous winter (clear-cut, CC). Tree harvesting reduced soil CO2 emission from ???22.5 to ???9.1 mol CO2??m2 for the 1994 growing season. OJP was a small net sink of atmospheric CO2, while CC was a net source of CO2. Winter emissions were similar at both sites. Reduction of soil respiration was attributed to disruption of the soil surface and to the death of tree roots. Flux simulations for CC and OJP identify 40% of CO2 emission at the undisturbed OJP site as near-surface respiration, 25% as deep-soil respiration, and 35% as tree-root respiration. The near-surface component was larger than the estimated annual C input to soil, suggesting fast C turnover and no net C accumulation in these boreal uplands in 1994.

Energy and material balance of CO2 capture from ambient air.

PubMed

Zeman, Frank

2007-11-01

Current Carbon Capture and Storage (CCS) technologies focus on large, stationary sources that produce approximately 50% of global CO2 emissions. We propose an industrial technology that captures CO2 directly from ambient air to target the remaining emissions. First, a wet scrubbing technique absorbs CO2 into a sodium hydroxide solution. The resultant carbonate is transferred from sodium ions to calcium ions via causticization. The captured CO2 is released from the calcium carbonate through thermal calcination in a modified kiln. The energy consumption is calculated as 350 kJ/mol of CO2 captured. It is dominated by the thermal energy demand of the kiln and the mechanical power required for air movement. The low concentration of CO2 in air requires a throughput of 3 million cubic meters of air per ton of CO2 removed, which could result in significant water losses. Electricity consumption in the process results in CO2 emissions and the use of coal power would significantly reduce to net amount captured. The thermodynamic efficiency of this process is low but comparable to other "end of pipe" capture technologies. As another carbon mitigation technology, air capture could allow for the continued use of liquid hydrocarbon fuels in the transportation sector.

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

NASA Astrophysics Data System (ADS)

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

2016-05-01

About 70 % of the anthropogenic carbon dioxide (CO2) is emitted from the megacities and urban areas of the world. In order to draw effective emission mitigation policies for combating future climate change as well as independently validating the emission inventories for constraining their large range of uncertainties, especially over major metropolitan areas of developing countries, there is an urgent need for greenhouse gas measurements over representative urban regions. India is a fast developing country, where fossil fuel emissions have increased dramatically in the last three decades and are predicted to continue to grow further by at least 6 % per year through to 2025. The CO2 measurements over urban regions in India are lacking. To overcome this limitation, simultaneous measurements of CO2 and carbon monoxide (CO) have been made at Ahmedabad, a major urban site in western India, using a state-of-the-art laser-based cavity ring down spectroscopy technique from November 2013 to May 2015. These measurements enable us to understand the diurnal and seasonal variations in atmospheric CO2 with respect to its sources (both anthropogenic and biospheric) and biospheric sinks. The observed annual average concentrations of CO2 and CO are 413.0 ± 13.7 and 0.50 ± 0.37 ppm respectively. Both CO2 and CO show strong seasonality with lower concentrations (400.3 ± 6.8 and 0.19 ± 0.13 ppm) during the south-west monsoon and higher concentrations (419.6 ± 22.8 and 0.72 ± 0.68 ppm) during the autumn (SON) season. Strong diurnal variations are also observed for both the species. The common factors for the diurnal cycles of CO2 and CO are vertical mixing and rush hour traffic, while the influence of biospheric fluxes is also seen in the CO2 diurnal cycle. Using CO and CO2 covariation, we differentiate the anthropogenic and biospheric components of CO2 and found significant contributions of biospheric respiration and anthropogenic emissions in the late night (00:00-05:00 h, IST) and evening rush hours (18:00-22:00 h) respectively. We compute total yearly emissions of CO to be 69.2 ± 0.07 Gg for the study region using the observed CO : CO2 correlation slope and bottom-up CO2 emission inventory. This calculated emission of CO is 52 % larger than the estimated emission of CO by the emissions database for global atmospheric research (EDGAR) inventory. The observations of CO2 have been compared with an atmospheric chemistry-transport model (ACTM), which incorporates various components of CO2 fluxes. ACTM is able to capture the basic variabilities, but both diurnal and seasonal amplitudes are largely underestimated compared to the observations. We attribute this underestimation by the model to uncertainties in terrestrial biosphere fluxes and coarse model resolution. The fossil fuel signal from the model shows fairly good correlation with observed CO2 variations, which supports the overall dominance of fossil fuel emissions over the biospheric fluxes in this urban region.

Experimental Study on NO Emission Concentration of Pulverized Coal in Different Atmosphere

NASA Astrophysics Data System (ADS)

Song, Jinghui; Yuan, Hui; Deng, jianhua

2018-02-01

The NO emission of pulverized coal during combustion in the O2/N2 atmosphere and O2/CO2 atmosphere was studied by using the sedimentation furnace test bed. The effects of CO2 concentration, temperature and excess air concentration on the NO emission characteristics of single coal and mixed coal The results show that the NO content of the pulverized coal is lower than that of the O2/N2 combustion atmosphere, and the decrease of the NO content in the O2/CO2 atmosphere is about 30%~35%. When the CO2 concentration changes from 20% to 50% of the process, the amount of NO produced in the selected coal gradually decreased, the change range is not large; with the pulverized coal combustion temperature continues to rise, the selected coal in the two kinds of atmosphere combustion NO content increased And the NO emission concentration is more obvious in the O2/N2 atmosphere. When the temperature reaches 1200°C and 1500°C the slope of the NO emission curve can be found to vary greatly. With the increase of the excess air coefficient α Increase, in these two atmosphere NO production also showed a rising trend.

Economic implications of reducing carbon emissions from energy use and industrial processes in Brazil.

PubMed

Chen, Y-H Henry; Timilsina, Govinda R; Landis, Florian

2013-11-30

This study assesses the economy-wide impacts of cutting CO2 emissions on the Brazilian economy. It finds that in 2040, the business-as-usual CO2 emissions from energy use and industrial processes would be almost three times as high as those in 2010 and would account for more than half of total national CO2 emissions. The current policy aims to reduce deforestation by 70 percent by 2017 and lower emissions intensity of the overall economy by 36-39 percent by 2020. If the policy were implemented as planned and continued to 2040, there would be no need to cut CO2 emissions from energy use and industrial processes until 2035, as emissions reduction through controlling deforestation would be enough to meet the voluntary carbon mitigation target of Brazil. The study also finds that using the carbon tax revenue to subsidize wind power can effectively increase the country's wind power output if that is the policy priority. Further, it finds evidence supporting the double dividend hypothesis, i.e., using revenue from a hypothetical carbon tax to finance a cut in labor income tax can significantly lower the GDP impacts of the carbon tax. Copyright © 2013 Elsevier Ltd. All rights reserved.

High-resolution atmospheric inversion of urban CO2 emissions during the dormant season of the Indianapolis Flux Experiment (INFLUX)

NASA Astrophysics Data System (ADS)

Lauvaux, Thomas; Miles, Natasha L.; Deng, Aijun; Richardson, Scott J.; Cambaliza, Maria O.; Davis, Kenneth J.; Gaudet, Brian; Gurney, Kevin R.; Huang, Jianhua; O'Keefe, Darragh; Song, Yang; Karion, Anna; Oda, Tomohiro; Patarasuk, Risa; Razlivanov, Igor; Sarmiento, Daniel; Shepson, Paul; Sweeney, Colm; Turnbull, Jocelyn; Wu, Kai

2016-05-01

Based on a uniquely dense network of surface towers measuring continuously the atmospheric concentrations of greenhouse gases (GHGs), we developed the first comprehensive monitoring systems of CO2 emissions at high resolution over the city of Indianapolis. The urban inversion evaluated over the 2012-2013 dormant season showed a statistically significant increase of about 20% (from 4.5 to 5.7 MtC ± 0.23 MtC) compared to the Hestia CO2 emission estimate, a state-of-the-art building-level emission product. Spatial structures in prior emission errors, mostly undetermined, appeared to affect the spatial pattern in the inverse solution and the total carbon budget over the entire area by up to 15%, while the inverse solution remains fairly insensitive to the CO2 boundary inflow and to the different prior emissions (i.e., ODIAC). Preceding the surface emission optimization, we improved the atmospheric simulations using a meteorological data assimilation system also informing our Bayesian inversion system through updated observations error variances. Finally, we estimated the uncertainties associated with undetermined parameters using an ensemble of inversions. The total CO2 emissions based on the ensemble mean and quartiles (5.26-5.91 MtC) were statistically different compared to the prior total emissions (4.1 to 4.5 MtC). Considering the relatively small sensitivity to the different parameters, we conclude that atmospheric inversions are potentially able to constrain the carbon budget of the city, assuming sufficient data to measure the inflow of GHG over the city, but additional information on prior emission error structures are required to determine the spatial structures of urban emissions at high resolution.

Characterization of fine particle and gaseous emissions during school bus idling.

PubMed

Kinsey, J S; Williams, D C; Dong, Y; Logan, R

2007-07-15

The particulate matter (PM) and gaseous emissions from six diesel school buses were determined over a simulated waiting period typical of schools in the northeastern U.S. Testing was conducted for both continuous idle and hot restart conditions using a suite of on-line particle and gas analyzers installed in the U.S. Environmental Protection Agency's Diesel Emissions Aerosol Laboratory. The specific pollutants measured encompassed total PM-2.5 mass (PM < or = 2.5 microm in aerodynamic diameter), PM-2.5 number concentration, particle size distribution, particle-surface polycyclic aromatic hydrocarbons (PAHs), and a tracer gas (1,1,1,2,3,3,3-heptafluoropropane) in the diluted sample stream. Carbon monoxide (CO), carbon dioxide, nitrogen oxides (NO(x)), total hydrocarbons (THC), oxygen, formaldehyde, and the tracer gas were also measured in the raw exhaust. Results of the study showed little difference in the measured emissions between a 10 min post-restart idle and a 10 min continuous idle with the exception of THC and formaldehyde. However, an emissions pulse was observed during engine restart. A predictive equation was developed from the experimental data, which allows a comparison between continuous idle and hot restart for NO(x), CO, PM2.5, and PAHs and which considers factors such as the restart emissions pulse and periods when the engine is not running. This equation indicates that restart is the preferred operating scenario as long as there is no extended idling after the engine is restarted.

Mapping palm oil expansion using SAR to study the impact on the CO2 cycle

NASA Astrophysics Data System (ADS)

Pohl, Christine

2014-06-01

With Malaysia being the second largest palm oil producer in the world and the fact that palm oil ranks first in vegetable oil production on the world market the palm oil industry became an important factor in the country. Along with the expansion of palm oil across the nation causing deforestation of natural rain forest and conversion of peat land into plantation land there are several factors causing a tremendous increase in carbon dioxide (CO2) emissions. Main causes of CO2 emission apart from deforestation and peat-land conversion are the fires to create plantation land plus the fires burning waste products of the plantations itself. This paper describes a project that aims at the development of a remote sensing monitoring system to allow a continuous observation of oil palm plantation activities and expansion in order to be able to quantify CO2 emissions. The research concentrates on developing a spaceborne synthetic aperture radar information extraction system for palm oil plantations in the Tropics. This will lead to objective figures that can be used internationally to create a policy implementation plan to sustainably reduce CO2 emission in the future.

Reducing CO2 flux by decreasing tillage in Ohio: overcoming conjecture with data

USDA-ARS?s Scientific Manuscript database

Soil could become an important sink for atmospheric carbon dioxide (CO2) as global agricultural greenhouse gas emissions continue to grow, but data to support this conjecture are few. Sequestering soil carbon (C) depends upon many factors including soil type, climate, crop, tillage, nitrogen fertili...

Factors and characteristics of ammonia, hydrogen sulfide, carbon dioxide, and particulate matter emissions from two manure-belt layer hen houses

NASA Astrophysics Data System (ADS)

Ni, Ji-Qin; Diehl, Claude A.; Chai, Lilong; Chen, Yan; Heber, Albert J.; Lim, Teng-Teeh; Bogan, Bill W.

2017-05-01

Manure-belt layer hen houses are a relatively newer design and are replacing the old high-rise layer hen houses for egg production in USA. However, reliable aerial pollutant emission data from comprehensive and long-term on-farm monitoring at manure-belt houses are scarce. This paper reports the emission factors and characteristics of ammonia (NH3), hydrogen sulfide (H2S), carbon dioxide (CO2), and particulate matter (PM10) from two 250,000-bird capacity manure-belt layer hen houses (B-A and B-B) in northern Indiana, USA. The 2-year continuous field monitoring followed the Quality Assurance Project Plan of the National Air Emission Monitoring Study (NAEMS). Only days with more than 18 h (or 75%) of valid data were reported to avoid biased emission calculation. The results of 2-year average daily mean (ADM) gas emissions per hen from the two houses, excluding emissions from their manure shed, were 0.280 g for NH3, 1.952 mg for H2S, and 103.2 g for CO2. They were 67% lower for NH3, 77% higher for H2S, and 10% higher for CO2 compared with reported emissions from high-rise layer hen houses. Emissions of NH3 and CO2 exhibited evident seasonal variations. They were higher in winter than in summer and followed the NH3 and CO2 concentration seasonal patterns. Annual emission differences were observed for all the four pollutants. Reduced emissions of the three gases were shown during periods of layer hen molting and flock replacement. The 2-year ADM PM10 emission from B-B was 25.2 mg d-1 hen-1. A unique weekly PM10 emission pattern was identified for both houses. It was characterized with much lower Sunday emissions compared with the other single-day emissions of the week and was related to the weekly schedule of in-house production operations, including maintenance and cleaning.

Tracking greenhouse gas emissions from a U.S. megacity by remote sensing from a mountaintop site

NASA Astrophysics Data System (ADS)

Wong, Clare; Fu, Dejian; Pongetti, Thomas; Newman, Sally; Kort, Eric; Duren, Riley; Hsu, Ying-Kuang; Miller, Charles; Yung, Yuk; Sander, Stanley

2014-05-01

Cities, such as Los Angeles, are significant sources of anthropogenic greenhouse gases (GHGs). With the growth of populations in cities worldwide, GHG emissions will increase, and monitoring the temporal trends will provide crucial data for global climate models as well as assessments of the effectiveness of control policies. Currently, continuous GHG observations in the Los Angeles basin are limited to a few in situ measurements, which are shown to be sensitive to local emissions and do not represent the Los Angeles basin well. To quantify GHG emissions from the metropolitan area, which tend to have heterogeneous characteristics, it is important to perform measurements which provide both continuous temporal and spatial coverage of the domain. Here we present observations of the major greenhouse gases, CO2 and CH4, using a spectroscopic remote sensing technique from the California Laboratory for Atmospheric Remote Sensing (CLARS) at Mount Wilson, California (1.7 km elevation). A Fourier Transform Spectrometer (FTS) deployed at the CLARS site points downward at 28 selected land surfaces in the LA basin to measure the slant column abundances of CO2, CH4, N2¬O, CO and O2 using reflected sunlight in the near-infrared and short-wave infrared regions. This remote sensing technique provides continuous temporal and spatial measurements in the Los Angeles basin to achieve the goal of quantifying emissions of GHGs and CO. It also serves as a test-bed for future geostationary satellite missions to measure GHGs from space such as NASA JPL's Geostationary Carbon Process Investigation (GCPI). The path-averaged dry-air mixing ratio, XCO2 and XCH4, observed by the CLARS FTS, showed significant diurnal variability that arises from emissions in the Los Angeles basin and atmospheric transport processes. High-precision data have been collected since August 2011. We analyze the seasonal trends of the ratio XCH4:XCO2 and estimate the seasonal and annual CH4 emission in the Los Angeles basin observed by the CLARS FTS from August 2011 to present. This work demonstrates the ability to quantify and track GHG emissions in a megacity using ground-based remote sensing from an elevated platform and the potential for future geostationary satellite missions, such as GCPI, to monitor carbon fluxes in cities. Copyright 2014. California Institute of Technology. Government sponsorship acknowledged.

Greenhouse Gas Emissions from U.S. Hydropower Reservoirs: FY2011 Annual Progress Report

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

Stewart, Arthur J; Mosher, Jennifer J; Mulholland, Patrick J

2012-05-01

The primary objective of this study is to quantify the net emissions of key greenhouse gases (GHG) - notably, CO{sub 2} and CH{sub 4} - from hydropower reservoirs in moist temperate areas within the U.S. The rationale for this objective is straightforward: if net emissions of GHG can be determined, it would be possible to directly compare hydropower to other power-producing methods on a carbon-emissions basis. Studies of GHG emissions from hydropower reservoirs elsewhere suggest that net emissions can be moderately high in tropical areas. In such areas, warm temperatures and relatively high supply rates of labile organic matter canmore » encourage high rates of decomposition, which (depending upon local conditions) can result in elevated releases of CO{sub 2} and CH{sub 4}. CO{sub 2} and CH{sub 4} emissions also tend to be higher for younger reservoirs than for older reservoirs, because vegetation and labile soil organic matter that is inundated when a reservoir is created can continue to decompose for several years (Galy-Lacaux et al. 1997, Barros et al. 2011). Water bodies located in climatically cooler areas, such as in boreal forests, could be expected to have lower net emissions of CO{sub 2} and CH{sub 4} because their organic carbon supplies tend to be relatively recalcitrant to microbial action and because cooler water temperatures are less conducive to decomposition.« less

A Review of CO2 Sequestration Projects and Application in China

PubMed Central

Tang, Yong; Yang, Ruizhi; Bian, Xiaoqiang

2014-01-01

In 2008, the top CO2 emitters were China, United States, and European Union. The rapid growing economy and the heavy reliance on coal in China give rise to the continued growth of CO2 emission, deterioration of anthropogenic climate change, and urgent need of new technologies. Carbon Capture and sequestration is one of the effective ways to provide reduction of CO2 emission and mitigation of pollution. Coal-fired power plants are the focus of CO2 source supply due to their excessive emission and the energy structure in China. And over 80% of the large CO2 sources are located nearby storage reservoirs. In China, the CO2 storage potential capacity is of about 3.6 × 109 t for all onshore oilfields; 30.483 × 109 t for major gas fields between 900 m and 3500 m of depth; 143.505 × 109 t for saline aquifers; and 142.67 × 109 t for coal beds. On the other hand, planation, soil carbon sequestration, and CH4–CO2 reforming also contribute a lot to carbon sequestration. This paper illustrates some main situations about CO2 sequestration applications in China with the demonstration of several projects regarding different ways of storage. It is concluded that China possesses immense potential and promising future of CO2 sequestration. PMID:25302323

COCA: deriving urban emissions and the carbon exchange of a forested region using airborne CO2 and CO observations

NASA Astrophysics Data System (ADS)

Geiss, H.; Schmitgen, S.; Ciais, P.; Neininger, B.; Baeumle, M.; Brunet, Y.; Kley, D.

2002-05-01

A crucial challenge in measuring the partitioning of sources and sinks of atmospheric CO2 is the separation of regional anthropogenic CO2 sources from biogenic activity. The aim of the COCA project is to quantify the fossil fuel and biogenic CO2 fractions using continuous airborne CO2 and CO measurements, where CO acts as a tracer for anthropogenic CO2. At first part of the project COCA an attempt was made to measure daytime biogenic CO2 fluxes over a forest area (about 15 by 30 km size). The campaign took place around the CARBOEUROFLUX site ``Le Bray'' (Pinus pinaster) close to Bordeaux in France end of June 2001 Based on continuous airborne CO2, H2O and CO flux and concentration measurements a Lagrangian budgeting approach was chosen to measure regional CO2 deposition fluxes. The objective is to determine the CO2 uptake of the extended forest area from the CO2/CO gradients up- and downwind of the ecosystem, using CO as air mass tracer and such estimating the influence of anthropogenic CO2 advected into the area First results of the summer flight on June 23rd will be shown, where fair wind speeds (~5 m/s) and a low CBL height led to the observation of a clear decrease in CO2 at the downwind flight stacks with basically constant CO concentrations. For other summer flights with very low wind speeds, local effects dominate the observations leading to a larger variability in the observations. Both, correlations and anti-correlations of CO2 with the anthropogenic tracer CO have been observed. Positive correlations indicate fresh plumes of anthropogenic CO2. Negative correlations are indicative of entrainment of free tropospheric air, that was marked by relatively higher CO2 and lower CO concentrations than the average CBL concentrations. During a second campaign the variance of anthropogenic CO and CO2 emissions of a large city unaffected by biogenic processes has been studied. This campaign was carried out on February 16 and 17, 2002 over the Paris metropolitan area (Ile de France, about 100 by 100 km size). Correlation plots of the measurements in the Paris plume on February 16th show a clear correlation between CO and CO2. This confirms the suitability of CO as a tracer for anthropogenic emissions at regional scales where the inputs of primary CO and CO2 with different ratios have blended to define regional mean CO/CO2 ratios.

40 CFR 98.146 - Data reporting requirements.

Code of Federal Regulations, 2010 CFR

2010-07-01

... (CONTINUED) MANDATORY GREENHOUSE GAS REPORTING Glass Production § 98.146 Data reporting requirements. In... glass melting furnace and for all furnaces combined (tons). (2) Annual quantity of glass produced (tons). (b) If a CEMS is not used to determine CO2 emissions from continuous glass melting furnaces, and...

Application of the LI-COR CO2 analyzer to volcanic plumes: a case study, volcán Popocatépetl, Mexico, June 7 and 10, 1995

USGS Publications Warehouse

Gerlach, T.M.; Delgado, H.; McGee, K.A.; Doukas, M.P.; Venegas, J.J.; Cardenas, L.

1997-01-01

Volcanic CO2 emission rate data are sparse despite their potential importance for constraining the role of magma degassing in the biogeochemical cycle of carbon and for assessing volcanic hazards. We used a LI-COR CO2 analyzer to determine volcanic CO2 emission rates by airborne measurements in volcanic plumes at Popocatépetl volcano on June 7 and 10, 1995. LI-COR sample paths of ∼72 m, compared with ∼1 km for the analyzer customarily used, together with fast Fourier transforms to remove instrument noise from raw data greatly improve resolution of volcanic CO2 anomalies. Parametric models fit to background CO2 provide a statistical tool for distinguishing volcanic from ambient CO2. Global Positioning System referenced flight traverses provide vastly improved data on the shape, coherence, and spatial distribution of volcanic CO2 in plume cross sections and contrast markedly with previous results based on traverse stacking. The continuous escape of CO2 and SO2 from Popocatépetl was fundamentally noneruptive and represented quiescent magma degassing from the top of a magma chamber ∼5 km deep. The average CO2 emission rate for January-June 1995 is estimated to be at least 6400 t d−1, one of the highest determined for a quiescently degassing volcano, although correction for downwind dispersion effects on volcanic CO2 indicates a higher rate of ∼9000 t d−1. Analysis of random errors indicates emission rates have 95% confidence intervals of ∼±20%, with uncertainty contributed mostly by wind speed variance, although the variance of plume cross-sectional areas during traversing is poorly constrained and possibly significant.

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.

Identifying Anthropogenic Emissions of Atmospheric Mercury and Methane in Urban Houston Using Measurements from A Mobile Laboratory

NASA Astrophysics Data System (ADS)

Lan, X.; Laine, P. L.; Talbot, R. W.; Lefer, B. L.; Flynn, J. H.; Sive, B. C.

2013-12-01

The Houston area is heavily polluted with more than 400 refineries and other industrial facilities in the surrounding regions. From our 2-year continuous measurements at this area, we observed frequent occurrences of large peaks in both atmospheric mercury and methane. The highest elemental mercury level we observed was 27,327 ppqv, and the highest CH4 level reached 25 ppmv. We found that some mercury spikes occurred simultaneously with peaks in CH4, CO, CO2, and NO. Many high mercury episodes showed different features of CO, CO2, CH4, NOx and SO2, indicating contributions from different sources. To identify and quantify the sources of mercury and methane in this area, a mobile van equipped with mercury instruments together with CH4, CO2, δ13CH4, δ13CO2 (Picarro G2201-i), and CO, O3, and NOx will be used to sample the emissions from surrounding oil refineries facilities, natural gas processing plants, coal-fired power plants, sewage treatment plants, landfills, petrochemical manufacturing facilities, etc. A Proton Transfer Reaction Mass Spectrometer is also equipped in the mobile van to measure some VOCs species, such as benzene, toluene, isoprene, acetaldehyde, formaldehyde, methanol, acetone, MVK, MEK+MACR, C8 aromatics. The CH4 isotopic and VOCs signatures, and the ratios of mercury versus important species (i.e., CO and CO2) will help us to identify the mercury and methane sources, to investigate the methane leakage problem from natural gas operations, and improve the mercury and methane emission inventories in Houston area. We believe this study will also provide important information on industrial emissions that are missing from the EPA National Emission Inventory.

40 CFR 90.328 - Measurement equipment accuracy/calibration frequency table.

Code of Federal Regulations, 2010 CFR

2010-07-01

... (CONTINUED) AIR PROGRAMS (CONTINUED) CONTROL OF EMISSIONS FROM NONROAD SPARK-IGNITION ENGINES AT OR BELOW 19... analyzers meet the water rejection ratio and the CO2 rejection ratio as specified in § 90.325. (g) Verify...

Increased N2O emission by inhibited plant growth in the CO2 leaked soil environment: Simulation of CO2 leakage from carbon capture and storage (CCS) site.

PubMed

Kim, You Jin; He, Wenmei; Ko, Daegeun; Chung, Haegeun; Yoo, Gayoung

2017-12-31

Atmospheric carbon dioxide (CO 2 ) concentrations is continuing to increase due to anthropogenic activity, and geological CO 2 storage via carbon capture and storage (CCS) technology can be an effective way to mitigate global warming due to CO 2 emission. However, the possibility of CO 2 leakage from reservoirs and pipelines exists, and such leakage could negatively affect organisms in the soil environment. Therefore, to determine the impacts of geological CO 2 leakage on plant and soil processes, we conducted a greenhouse study in which plants and soils were exposed to high levels of soil CO 2 . Cabbage, which has been reported to be vulnerable to high soil CO 2 , was grown under BI (no injection), NI (99.99% N 2 injection), and CI (99.99% CO 2 injection). Mean soil CO 2 concentration for CI was 66.8-76.9% and the mean O 2 concentrations in NI and CI were 6.6-12.7%, which could be observed in the CO 2 leaked soil from the pipelines connected to the CCS sites. The soil N 2 O emission was increased by 286% in the CI, where NO 3 - -N concentration was 160% higher compared to that in the control. This indicates that higher N 2 O emission from CO 2 leakage could be due to enhanced nitrification process. Higher NO 3 - -N content in soil was related to inhibited plant metabolism. In the CI treatment, chlorophyll content decreased and chlorosis appeared after 8th day of injection. Due to the inhibited root growth, leaf water and nitrogen contents were consistently lowered by 15% under CI treatment. Our results imply that N 2 O emission could be increased by the secondary effects of CO 2 leakage on plant metabolism. Hence, monitoring the environmental changes in rhizosphere would be very useful for impact assessment of CCS technology. Copyright © 2017 Elsevier B.V. All rights reserved.

40 CFR 75.1 - Purpose and scope.

Code of Federal Regulations, 2014 CFR

2014-07-01

... monitoring systems and provisions to account for missing data from certified continuous emission monitoring... estimation procedures for missing data are included in appendix C to this part. Optional protocols for...), and carbon dioxide (CO2) emissions, volumetric flow, and opacity data from affected units under the...

40 CFR 75.1 - Purpose and scope.

Code of Federal Regulations, 2011 CFR

2011-07-01

... monitoring systems and provisions to account for missing data from certified continuous emission monitoring... estimation procedures for missing data are included in appendix C to this part. Optional protocols for...), and carbon dioxide (CO2) emissions, volumetric flow, and opacity data from affected units under the...

40 CFR 75.1 - Purpose and scope.

Code of Federal Regulations, 2013 CFR

2013-07-01

... monitoring systems and provisions to account for missing data from certified continuous emission monitoring... estimation procedures for missing data are included in appendix C to this part. Optional protocols for...), and carbon dioxide (CO2) emissions, volumetric flow, and opacity data from affected units under the...

Measurements of CO, CO2, OH, and H2O in room-temperature and combustion gases by use of a broadly current-tuned multisection InGaAsP diode laser.

PubMed

Upschulte, B L; Sonnenfroh, D M; Allen, M G

1999-03-20

A new laser technology that achieves nearly 100-nm quasi-continuous tuning with only injection-current control in a four-section grating-coupler sampled-reflector laser was used to detect CO and CO(2) simultaneously in room-temperature gas mixtures. The same grating-coupler sampled-reflector laser was used to perform in situ measurements of CO, H(2)O, and OH in the exhaust gases of a CH(4)-air flame. This laser is being evaluated for inclusion in a multispecies combustion-emissions exhaust-analysis sensor, and its operational characteristics as they have an impact on gas sensing are described. Preliminary results suggest that this single laser can be used to replace multilaser sensor configurations for some combustion-emissions monitoring applications.

Sources of greenhouse gases and carbon monoxide in central London (UK)

NASA Astrophysics Data System (ADS)

Helfter, Carole; Tremper, Anja; Zazzeri, Giulia; Barlow, Janet F.; Nemitz, Eiko

2015-04-01

Biosphere-atmosphere exchange of carbon dioxide (CO2) has been on the scientific agenda for several decades and new technology now also allows for high-precision, continuous monitoring of fluxes of methane (CH4) and nitrous oxide (N2O). Compared to the natural environment, flux measurements in the urban environment, which is home to over 50% of the population globally, are still rare despite high densities of anthropogenic sources of pollutants. We report on over three years of measurements atop a 192 m tower in central London (UK), Europe's largest city, which started in October 2011. Fluxes of methane, carbon monoxide (CO) and carbon dioxide are measured by eddy-covariance (EC) at the British Telecom tower (51° 31' 17.4' N 0° 8' 20.04' W). In addition to the long-term measurements, EC fluxes of nitrous oxide (N2O) were measured in February 2014. All four trace gases exhibit diurnal trends consistent with anthropogenic activities with minimum emissions at night and early afternoon maxima. Segregating emissions by wind direction reveals heterogeneous source distributions with temporal patterns and source strengths that differ between compounds. The lowest emissions for CO, CO2 and CH4 were recorded for NW winds. The highest emissions of methane were in the SE sector, in the NE for CO2 and in the W for CO. Fluxes of all 3 gases exhibited marked seasonal trends characterised by a decrease in emissions in summer (63% reduction for CO, 36% for CO2 and 22% for CH4). Monthly fluxes of CO and CO2 were linearly correlated to air temperature (R2 = 0.7 and 0.59 respectively); a weaker dependence upon temperature was also observed for CH4 (R2 = 0.31). Diurnal and seasonal emissions of CO and CO2 are mainly controlled by local fossil fuel combustion and vehicle cold starts are thought to account for 20-30% of additional emissions of CO during the winter. Fugitive emissions of CH4 from the natural gas distribution network are thought to be substantial, which is consistent with the weaker seasonality of CH4 fluxes compared with CO and CO2. Annual estimates of CO2 emissions (41 kt km-2) obtained by EC were consistent with data upscaled from the London Atmospheric Emissions Inventory (LAEI; 46 kt km-2). Good agreement between measurements and inventory data was also found for CO (measured 156 t km-2; LAEI 145 t km-2) and for N2O (measured 0.36 t km-2; LAEI 0.42 t km-2), although based on a much shorter measurement period. By contrast, a two-fold difference was found between inventory and measured CH4 fluxes (measured 75 t km-2; LAEI 34 t km-2), which could indicate an underestimation by the inventory of CH4 emissions from anthropogenic sources or the existence of unaccounted biogenic sources. Measurements of isotopic CH4 taken 2 km SE of the tower near the banks of the river Thames reveal multiple episodes of 13C-depleted morning peaks consistent with biogenic sources. We speculate that the Thames can act as an additional significant source of biogenic methane especially at low tide and after heavy rainfall, which could explain the large emissions observed in the S-SE sector.

Holocene peatland and ice-core data constraints on the timing and magnitude of CO2 emissions from past land use.

PubMed

Stocker, Benjamin David; Yu, Zicheng; Massa, Charly; Joos, Fortunat

2017-02-14

CO 2 emissions from preindustrial land-use change (LUC) are subject to large uncertainties. Although atmospheric CO 2 records suggest only a small land carbon (C) source since 5,000 y before present (5 kyBP), the concurrent C sink by peat buildup could mask large early LUC emissions. Here, we combine updated continuous peat C reconstructions with the land C balance inferred from double deconvolution analyses of atmospheric CO 2 and [Formula: see text]C at different temporal scales to investigate the terrestrial C budget of the Holocene and the last millennium and constrain LUC emissions. LUC emissions are estimated with transient model simulations for diverging published scenarios of LU area change and shifting cultivation. Our results reveal a large terrestrial nonpeatland C source after the Mid-Holocene (66 [Formula: see text] 25 PgC at 7-5 kyBP and 115 [Formula: see text] 27 PgC at 5-3 kyBP). Despite high simulated per-capita CO 2 emissions from LUC in early phases of agricultural development, humans emerge as a driver with dominant global C cycle impacts only in the most recent three millennia. Sole anthropogenic causes for particular variations in the CO 2 record ([Formula: see text]20 ppm rise after 7 kyBP and [Formula: see text]10 ppm fall between 1500 CE and 1600 CE) are not supported. This analysis puts a strong constraint on preindustrial vs. industrial-era LUC emissions and suggests that upper-end scenarios for the extent of agricultural expansion before 1850 CE are not compatible with the C budget thereafter.

40 CFR 98.147 - Records that must be retained.

Code of Federal Regulations, 2010 CFR

2010-07-01

... (CONTINUED) MANDATORY GREENHOUSE GAS REPORTING Glass Production § 98.147 Records that must be retained. In... paragraphs (a)(1) and (a)(2) of this section: (1) Monthly glass production rate for each continuous glass... glass melting furnace (tons). (b) If process CO2 emissions are calculated according to the procedures...

40 CFR 98.147 - Records that must be retained.

Code of Federal Regulations, 2011 CFR

2011-07-01

... (CONTINUED) MANDATORY GREENHOUSE GAS REPORTING Glass Production § 98.147 Records that must be retained. In... paragraphs (a)(1) and (a)(2) of this section: (1) Monthly glass production rate for each continuous glass... glass melting furnace (tons). (b) If process CO2 emissions are calculated according to the procedures...

Seasonal variations in elemental carbon aerosol, carbon monoxide and sulfur dioxide: Implications for sources

NASA Astrophysics Data System (ADS)

Antony Chen, L.-W.; Doddridge, Bruce G.; Dickerson, Russell R.; Chow, Judith C.; Mueller, Peter K.; Quinn, John; Butler, William A.

As part of Maryland Aerosol Research and CHaracterization (MARCH-Atlantic) study, measurements of 24-hr average elemental carbon (EC) aerosol concentration were made at Fort Meade, Maryland, USA, a suburban site within the Baltimore-Washington corridor during July 1999, October 1999, January 2000, April 2000 and July 2000. Carbon monoxide (CO) and sulfur dioxide (SO2) were also measured nearly continuously over the period. Tight correlation between EC and CO in every month suggests common or proximate sources, likely traffic emissions. The EC versus CO slope varies in different seasons and generally increases with ambient temperature. The temperature dependence of EC/CO ratios suggests that EC source strength peaks in summer. By using the well established emission inventory for CO, and EC/CO ratio found in this study, EC emission over North America is estimated at 0.31±0.12 Tg yr-1, on the low end but in reasonable agreement with prior inventories based on emission factors and fuel consumption.

Seasonal variations in elemental carbon aerosol, carbon monoxide and sulfur dioxide: Implications for sources

NASA Astrophysics Data System (ADS)

Chen, L.-W. Antony; Doddridge, Bruce G.; Dickerson, Russell R.; Chow, Judith C.; Mueller, Peter K.; Quinn, John; Butler, William A.

2001-05-01

As part of Maryland Aerosol Research and CHaracterization (MARCH-Atlantic) study, measurements of 24-hr average elemental carbon (EC) aerosol concentration were made at Fort Meade, Maryland, USA, a suburban site within the Baltimore-Washington corridor during July 1999, October 1999, January 2000, April 2000 and July 2000. Carbon monoxide (CO) and sulfur dioxide (SO2) were also measured nearly continuously over the period. Tight correlation between EC and CO in every month suggests common or proximate sources, likely traffic emissions. The EC versus CO slope varies in different seasons and generally increases with ambient temperature. The temperature dependence of EC/CO ratios suggests that EC source strength peaks in summer. By using the well established emission inventory for CO, and EC/CO ratio found in this study, EC emission over North America is estimated at 0.31+/-0.12Tgyr-1, on the low end but in reasonable agreement with prior inventories based on emission factors and fuel consumption.

Anthropogenic emissions of nonmethane hydrocarbons in the northeastern United States: Measured seasonal variations from 1992-1996 and 1999-2001

NASA Astrophysics Data System (ADS)

Lee, Ben H.; Munger, J. William; Wofsy, Steven C.; Goldstein, Allen H.

2006-10-01

Harvard Forest, a rural site located in central Massachusetts downwind of major urban-industrial centers, provides an excellent location to observe a typical regional mixture of anthropogenic trace gases. Air that arrives at Harvard Forest from the southwest is affected by emissions from the U.S. east coast urban corridor and may have residual influence from emissions in the upper Ohio Valley and Great Lakes region farther to the west. Because of its relatively long distance from large individual emission sources, pollution plumes reaching the site are a homogenized mixture of regional anthropogenic emissions. Concentrations of C2-C6 hydrocarbons along with CO and NOy were measured nearly continuously from August 1992 through July 1996 and from June 1999 through November 2001. By correlating observed concentrations to acetylene, which is almost solely produced during combustion, we are able to detect seasonal trends in relative emissions for this series of trace gases. Seasonal changes in n-butane and i-butane emissions may largely be influenced by different gasoline formulations in late spring and summer. Shifts in evaporation rates due to the annual temperature cycle could induce a seasonal pattern for n-pentane, i-pentane and n-hexane emissions. Emissions of ethane and propane lack clear seasonality relative to acetylene emissions and also correlate less with acetylene than other gases, indicating that emissions of these two gases are strongly influenced by sources not associated with fuel combustion. Changes in the observed correlations of CO2 and CO relative to acetylene are consistent with published changes in the estimated emissions of CO2 and CO over the past decade, though variability in the observations makes it difficult to precisely quantify these changes.

CO2 and CH4 fluxes in a Spartina salt marsh and brackish Phragmites marsh in Massachusetts

NASA Astrophysics Data System (ADS)

Tang, J.; Wang, F.; Kroeger, K. D.; Gonneea, M. E.

2017-12-01

Coastal salt marshes play an important role in global and regional carbon cycling. Tidally restricted marshes reduce salinity and provide a habitat suitable for Phragmites invasion. We measured greenhouse gas (GHG) emissions (CO2 and CH4) continuously with the eddy covariance method and biweekly with the static chamber method in a Spartina salt marsh and a Phragmites marsh on Cape Cod, Massachusetts, USA. We did not find significant difference in CO2 fluxes between the two sites, but the CH4 fluxes were much higher in the Phragmites site than the Spartina marsh. Temporally, tidal cycles influence the CO2 and CH4 fluxes in both sites. We found that the salt marsh was a significant carbon sink when CO2 and CH4 fluxes were combined. Restoring tidally restricted marshes will significantly reduce CH4 emissions and provide a strong ecosystem carbon service.

Remote sensing of trend and seasonal variability of greenhouse gas emissions from the Los Angeles basin using an FTS on Mount Wilson

NASA Astrophysics Data System (ADS)

Wong, C.; Fu, D.; Pongetti, T. J.; Newman, S.; Yung, Y. L.; Sander, S. P.

2013-12-01

Cities, such as Los Angeles, are significant sources of anthropogenic greenhouse gases (GHGs). With the growth of populations in cities worldwide, GHG emissions will increase, and monitoring the temporal trends will provide crucial data for global climate models as well as assessments of the effectiveness of control policies. Currently, continuous GHG observations in the Los Angeles basin are limited to a few in situ measurements, which are shown to be sensitive to local emissions and do not represent the Los Angeles basin well. To quantify GHG emissions from the metropolitan area, which tend to have heterogeneous characteristics, it is important to perform measurements which provide both continuous temporal and spatial coverage of the domain. Here we present observations of the major greenhouse gases, CO2 and CH4, using a spectroscopic remote sensing technique from the California Laboratory for Atmospheric Remote Sensing (CLARS) at Mount Wilson, California (1.7 km elevation). A Fourier Transform Spectrometer (FTS) deployed at the CLARS site points downward at 28 selected land surfaces in the Los Angeles basin to measure the slant column abundances of CO2, CH4, N2O, CO and O2 using reflected sunlight in the near-infrared and shortwave infrared regions. This remote sensing technique provides continuous temporal and spatial measurements in the Los Angeles basin to achieve the goal of quantifying emissions of GHGs and CO. It also serves as a test-bed for future geostationary satellite missions to measure GHGs from space such as JPL's Geostationary Carbon Process Investigation (GCPI). The path-averaged dry-air mixing ratio, XCO2 and XCH4, observed by the CLARS FTS, show significant diurnal variability that arises from emissions in the Los Angeles basin and atmospheric transport processes. High-precision data have been collected since August 2011. Here we analyze the annual and seasonal trend of the ratio XCH4:XCO2 in the Los Angeles basin observed by the CLARS FTS from August 2011 to present. This work demonstrates the ability to quantify and track GHG emissions in a megacity using ground-based remote sensing from an elevated platform and the potential for future geostationary satellite missions, such as GCPI, to monitor carbon fluxes in cities.

Gas phase oxidation downstream of a catalytic combustor

NASA Technical Reports Server (NTRS)

Tien, J. S.; Anderson, D. N.

1979-01-01

Effect of the length available for gas-phase reactions downstream of the catalytic reactor on the emission of CO and unburned hydrocarbons was investigated. A premixed, prevaporized propane/air feed to a 12/cm/diameter catalytic/reactor test section was used. The catalytic reactor was made of four 2.5 cm long monolithic catalyst elements. Four water cooled gas sampling probes were located at positions between 0 and 22 cm downstream of the catalytic reactor. Measurements of unburned hydrocarbon, CO, and CO2 were made. Tests were performed with an inlet air temperature of 800 K, a reference velocity of 10 m/s, pressures of 3 and 600,000 Pa, and fuel air equivalence ratios of 0.14 to 0.24. For very lean mixtures, hydrocarbon emissions were high and CO continued to be formed downstream of the catalytic reactor. At the highest equivalence ratios tested, hydrocarbon levels were much lower and CO was oxidized to CO2 in the gas phase downstream. To achieve acceptable emissions, a downstream region several times longer than the catalytic reactor could be required.

40 CFR Appendix to Subpart Eee of... - Quality Assurance Procedures for Continuous Emissions Monitors Used for Hazardous Waste Combustors

Code of Federal Regulations, 2014 CFR

2014-07-01

... and CEMS control capabilities. 2.2Relative Accuracy (RA). The absolute mean difference between the... readings at the zero pollutant level after a stated period of operation during which no unscheduled... Evaluation for CO, O2, and HC CEMS Carbon Monoxide (CO), Oxygen (O2), and Hydrocarbon (HC) CEMS. An Absolute...

40 CFR Appendix to Subpart Eee of... - Quality Assurance Procedures for Continuous Emissions Monitors Used for Hazardous Waste Combustors

Code of Federal Regulations, 2013 CFR

2013-07-01

... and CEMS control capabilities. 2.2Relative Accuracy (RA). The absolute mean difference between the... readings at the zero pollutant level after a stated period of operation during which no unscheduled... Evaluation for CO, O2, and HC CEMS Carbon Monoxide (CO), Oxygen (O2), and Hydrocarbon (HC) CEMS. An Absolute...

A compilation of sulfur dioxide and carbon dioxide emission-rate data from Cook Inlet volcanoes (Redoubt, Spurr, Iliamna, and Augustine), Alaska during the period from 1990 to 1994

USGS Publications Warehouse

Doukas, Michael P.

1995-01-01

Airborne sulfur dioxide (SO2) gas sampling of the Cook Inlet volcanoes (Mt. Spurr, Redoubt, Iliamna, and Augustine) began in 1986 when several measurements were carried out at Augustine volcano during the eruption of 1986 (Rose and others, 1988). More systematic monitoring for SO2 began in March 1990 and for carbon dioxide (CO2) began in June, 1990 at Redoubt Volcano (Brantley, 1990 and Casadevall and others, 1994) and continues to the present. This report contains all of the available daily SO2 and CO2 emission rates determined by the U.S. Geological Survey (USGS) from March 1990 through July 1994. Intermittent measurements (four to six month intervals) at Augustine and Iliamna began in 1990 and continues to the present. Intermittent measurements began at Mt. Spurr volcano in 1991, and were continued at more regular intervals from June, 1992 through the 1992 eruption at the Crater Peak vent to the present.

Diurnal and seasonal variation of various carbon fluxes from an urban tower platform in Houston, TX

NASA Astrophysics Data System (ADS)

Schade, G. W.; Werner, N.; Hale, M. C.

2013-12-01

We measured carbon fluxes (CO2, CO, VOCs) from a tall lattice tower in Houston between 2007 and 2009, and 2011-2013. We present results from various analyses of (i) anthropogenic and biogenic CO2 fluxes using a quadrant segregation technique, (ii) seasonal and multi-year changes of CO fluxes as related to car traffic and industrial sources, and (iii) the accuracy of, and usefulness of a bulk flux footprint model to quantify pentane emissions form a distant source in comparison to permitted emission levels. Segregated and net anthropogenic CO2 fluxes were dominated by car traffic but industrial sources were identified as well. Emissions sank to minimal levels after hurricane Ike had passed over Houston, causing a traffic shutdown and lower population density. Segregated biogenic fluxes showed a clear seasonal variation with photosynthetic activity between April and November, and large effects of the 2011 Texas drought due to negligible irrigation in the study area. Carbon monoxide fluxes, measured via a flux gradient technique, are even stronger dominated by car traffic than CO2 fluxes and serve as a traffic tracer. Our data show a continued drop in emissions over time, seasonal changes with higher emissions during winter, and local influences due to industrial emissions. Lastly, we present the results of a tracer release study and a single point source quantification to test a bulk footprint model in this complex urban area. Known releases of volatile acetone and MEK were compered to measured fluxes using a REA-GC-FID system, and permit emissions of pentane from a foam plastics manufacturing facility were compared to measured pentane fluxes. Both comparisons reveal a surprisingly accurate performance of the footprint model within a factor of 2.

Future land-use change emissions: CO2, BVOC and wildfire

NASA Astrophysics Data System (ADS)

Arneth, A.; Knorr, W.; Hantson, S.; Anthoni, P.; Szogs, S.

2015-12-01

Historical land-use (LUC) change is known to have been a large source of CO2 emissions, mostly from deforestation: the equivalent of around 1/3 of today's CO2 in the atmosphere arises from LUC. And LUC will continue into the future, although the expected area change, the type of LUC (deforestation vs. afforestation/reforestation) and regions where the LUC will take place will differ greatly, depending on the future scenario. But LUC is not only of importance for projecting emissions of CO2. It also affects greatly emissions of biogenic volatile organic carbon, and from wildfires - all of which are important for the quantification of precursor substances relevant to air quality, and interactions with climate change. We show here that accounting for future socio-economic developments and LUC scenarios has the potential to override climate change and effects of CO2 fertilisation on fire and BVOC emission, regionally and in some cases also globally. Simulation experiments with the dynamic global vegetation model LPJ-GUESS will be performed, covering the 20th and 21st century, and assessing a rage of future population growth, LUC and climate change scenarios. For wildfire emissions, we find that burned area and emissions depend greatly on the type of population growth scenario, and on the distribution of urban vs rural population. BVOC emissions depend greatly on the amount and location of deforestation vs the region and magnitude of forest expansion in response to warming, such as through expansion of vegetation in the northern hemisphere, and via reforestation/afforestation. LUC so far has not been given sufficient attention for simulations of future air quality-climate interactions. In terms of terrestrial precursor emissions of atmospherically reactive substances our simulations clearly demonstrate the importance of including LUC in combination with vegetation that responds dynamically to changes in climate and atmospheric CO2 levels.

Ocean acidification in a geoengineering context

PubMed Central

Williamson, Phillip; Turley, Carol

2012-01-01

Fundamental changes to marine chemistry are occurring because of increasing carbon dioxide (CO2) in the atmosphere. Ocean acidity (H+ concentration) and bicarbonate ion concentrations are increasing, whereas carbonate ion concentrations are decreasing. There has already been an average pH decrease of 0.1 in the upper ocean, and continued unconstrained carbon emissions would further reduce average upper ocean pH by approximately 0.3 by 2100. Laboratory experiments, observations and projections indicate that such ocean acidification may have ecological and biogeochemical impacts that last for many thousands of years. The future magnitude of such effects will be very closely linked to atmospheric CO2; they will, therefore, depend on the success of emission reduction, and could also be constrained by geoengineering based on most carbon dioxide removal (CDR) techniques. However, some ocean-based CDR approaches would (if deployed on a climatically significant scale) re-locate acidification from the upper ocean to the seafloor or elsewhere in the ocean interior. If solar radiation management were to be the main policy response to counteract global warming, ocean acidification would continue to be driven by increases in atmospheric CO2, although with additional temperature-related effects on CO2 and CaCO3 solubility and terrestrial carbon sequestration. PMID:22869801

Precursory diffuse CO2 and H2S emission signatures of the 2011-2012 El Hierro submarine eruption, Canary Islands

NASA Astrophysics Data System (ADS)

Pérez, Nemesio M.; Padilla, Germán D.; Padrón, Eleazar; Hernández, Pedro A.; Melián, Gladys V.; Barrancos, José; Dionis, Samara; Nolasco, Dácil; Rodríguez, Fátima; Calvo, David; Hernández, Íñigo

2012-08-01

On October 12, 2011, a submarine eruption began 2 km off the coast of La Restinga, south of El Hierro Island. CO2 and H2S soil efflux were continuously measured during the period of volcanic unrest by using the accumulation chamber method at two different geochemical stations, HIE01 and HIE07. Recorded CO2 and H2S effluxes showed precursory signals that preceded the submarine eruption. Beginning in late August, the CO2 efflux time series started increasing at a relatively constant rate over one month, reaching a maximum of 19 gm-2d-1 one week before the onset of the submarine volcanic eruption. The H2S efflux time series at HIE07 showed a pulse in H2S emission just one day before the initiation of the submarine eruption, reaching peak values of 42 mg m-2 d-1, 10 times the average H2S efflux recorded during the observation period. Since CO2 and H2S effluxes are strongly influenced by external factors, we applied a multiple regression analysis to remove their contribution. A statistical analysis showed that the long-term trend of the filtered data is well correlated with the seismic energy. We find that these geochemical stations are important monitoring sites for evaluating the volcanic activity of El Hierro and that they demonstrate the potential of applying continuous monitoring of soil CO2 and H2S efflux to improve and optimize the detection of early warning signals of future volcanic unrest episodes at El Hierro. Continuous diffuse degassing studies would likely prove useful for monitoring other volcanoes during unrest episodes.

Catalytic reduction of CO 2 by H 2 for synthesis of CO, methanol and hydrocarbons: challenges and opportunities

DOE PAGES

Porosoff, Marc D.; Yan, Binhang; Chen, Jingguang G.

2015-10-22

Ocean acidification and climate change are expected to be two of the most difficult scientific challenges of the 21st century. Converting CO 2 into valuable chemicals and fuels is one of the most practical routes for reducing CO 2 emissions while fossil fuels continue to dominate the energy sector. Reducing CO 2 by H 2 using heterogeneous catalysis has been studied extensively, but there are still significant challenges in developing active, selective and stable catalysts suitable for large-scale commercialization. We study the catalytic reduction of CO 2 by H 2 can lead to the formation of three types of products:more » CO through the reverse water–gas shift (RWGS) reaction, methanol via selective hydrogenation, and hydrocarbons through combination of CO 2 reduction with Fischer–Tropsch (FT) reactions. In addition, investigations into these routes reveal that the stabilization of key reaction intermediates is critically important for controlling catalytic selectivity. Furthermore, viability of these processes is contingent on the development of a CO 2-free H 2 source on a large enough scale to significantly reduce CO 2 emissions.« less

Assessment and Optimization of the Accuracy of an Aircraft-Based Technique Used to Quantify Greenhouse Gas Emission Rates from Point Sources

NASA Astrophysics Data System (ADS)

Shepson, P. B.; Lavoie, T. N.; Kerlo, A. E.; Stirm, B. H.

2016-12-01

Understanding the contribution of anthropogenic activities to atmospheric greenhouse gas concentrations requires an accurate characterization of emission sources. Previously, we have reported the use of a novel aircraft-based mass balance measurement technique to quantify greenhouse gas emission rates from point and area sources, however, the accuracy of this approach has not been evaluated to date. Here, an assessment of method accuracy and precision was performed by conducting a series of six aircraft-based mass balance experiments at a power plant in southern Indiana and comparing the calculated CO2 emission rates to the reported hourly emission measurements made by continuous emissions monitoring systems (CEMS) installed directly in the exhaust stacks at the facility. For all flights, CO2 emissions were quantified before CEMS data were released online to ensure unbiased analysis. Additionally, we assess the uncertainties introduced to the final emission rate caused by our analysis method, which employs a statistical kriging model to interpolate and extrapolate the CO2 fluxes across the flight transects from the ground to the top of the boundary layer. Subsequently, using the results from these flights combined with the known emissions reported by the CEMS, we perform an inter-model comparison of alternative kriging methods to evaluate the performance of the kriging approach.

The relationship between economic growth, energy consumption, and CO2 emissions: Empirical evidence from China.

PubMed

Wang, Shaojian; Li, Qiuying; Fang, Chuanglin; Zhou, Chunshan

2016-01-15

Following several decades of rapid economic growth, China has become the largest energy consumer and the greatest emitter of CO2 in the world. Given the complex development situation faced by contemporary China, Chinese policymakers now confront the dual challenge of reducing energy use while continuing to foster economic growth. This study posits that a better understanding of the relationship between economic growth, energy consumption, and CO2 emissions is necessary, in order for the Chinese government to develop the energy saving and emission reduction strategies for addressing the impacts of climate change. This paper investigates the cointegrating, temporally dynamic, and casual relationships that exist between economic growth, energy consumption, and CO2 emissions in China, using data for the period 1990-2012. The study develops a comprehensive conceptual framework in order to perform this analysis. The results of cointegration tests suggest the existence of long-run cointegrating relationship among the variables, albeit with short dynamic adjustment mechanisms, indicating that the proportion of disequilibrium errors that can be adjusted in the next period will account for only a fraction of the changes. Further, impulse response analysis (which describes the reaction of any variable as a function of time in response to external shocks) found that the impact of a shock in CO2 emissions on economic growth or energy consumption was only marginally significant. Finally, Granger casual relationships were found to exist between economic growth, energy consumption, and CO2 emissions; specifically, a bi-directional causal relationship between economic growth and energy consumption was identified, and a unidirectional causal relationship was found to exist from energy consumption to CO2 emissions. The findings have significant implications for both academics and practitioners, warning of the need to develop and implement long-term energy and economic policies in order to effectively address greenhouse effects in China, thereby setting the nation on a low-carbon growth path. Copyright © 2015 Elsevier B.V. All rights reserved.

Long-term changes in quiescent degassing at Mount Baker Volcano, Washington, USA; Evidence for a stalled intrusion in 1975 and connection to a deep magma source

USGS Publications Warehouse

Werner, Cynthia A.; Evans, William C.; Poland, Michael P.; Doukas, Michael P.; Tucker, D.S.

2009-01-01

Long-term changes have occurred in the chemistry, isotopic ratios, and emission rates of gas at Mount Baker volcano following a major thermal perturbation in 1975. In mid-1975 a large pulse in sulfur and carbon dioxide output was observed both in emission rates and in fumarole samples. Emission rates of CO2 and H2S were ??? 950 and 112??t/d, respectively, in 1975; these decreased to ??? 150 and < 1??t/d by 2007. During the peak of the activity the C/S ratio was the lowest ever observed in the Cascade Range and similar to magmatic signatures observed at other basaltic-andesite volcanoes worldwide. Increases in the C/S ratio and decreases in the CO2/CH4 ratio since 1975 suggest a long steady trend back toward a more hydrothermal gas signature. The helium isotope ratio is very high (> 7??Rc/RA), but has declined slightly since the mid-1970s, and ??13C-CO2 has decreased by ??? 1??? over time. Both trends are expected from a gradually crystallizing magma. While other scenarios are investigated, we conclude that magma intruded the mid- to shallow-crust beneath Mount Baker during the thermal awakening of 1975. Since that time, evidence for fresh magma has waned, but the continued emission of CO2 and the presence of a long-term hydrothermal system leads us to suspect some continuing connection between the surface and deep convecting magma.

CO2 Efflux from Cleared Mangrove Peat

PubMed Central

Lovelock, Catherine E.; Ruess, Roger W.; Feller, Ilka C.

2011-01-01

Background CO2 emissions from cleared mangrove areas may be substantial, increasing the costs of continued losses of these ecosystems, particularly in mangroves that have highly organic soils. Methodology/Principal Findings We measured CO2 efflux from mangrove soils that had been cleared for up to 20 years on the islands of Twin Cays, Belize. We also disturbed these cleared peat soils to assess what disturbance of soils after clearing may have on CO2 efflux. CO2 efflux from soils declines from time of clearing from ∼10 600 tonnes km−2 year−1 in the first year to 3000 tonnes km2 year−1 after 20 years since clearing. Disturbing peat leads to short term increases in CO2 efflux (27 umol m−2 s−1), but this had returned to baseline levels within 2 days. Conclusions/Significance Deforesting mangroves that grow on peat soils results in CO2 emissions that are comparable to rates estimated for peat collapse in other tropical ecosystems. Preventing deforestation presents an opportunity for countries to benefit from carbon payments for preservation of threatened carbon stocks. PMID:21738628

CO2 efflux from cleared mangrove peat.

PubMed

Lovelock, Catherine E; Ruess, Roger W; Feller, Ilka C

2011-01-01

CO(2) emissions from cleared mangrove areas may be substantial, increasing the costs of continued losses of these ecosystems, particularly in mangroves that have highly organic soils. We measured CO(2) efflux from mangrove soils that had been cleared for up to 20 years on the islands of Twin Cays, Belize. We also disturbed these cleared peat soils to assess what disturbance of soils after clearing may have on CO(2) efflux. CO(2) efflux from soils declines from time of clearing from ∼10,600 tonnes km(-2) year(-1) in the first year to 3000 tonnes km(2) year(-1) after 20 years since clearing. Disturbing peat leads to short term increases in CO(2) efflux (27 umol m(-2) s(-1)), but this had returned to baseline levels within 2 days. Deforesting mangroves that grow on peat soils results in CO(2) emissions that are comparable to rates estimated for peat collapse in other tropical ecosystems. Preventing deforestation presents an opportunity for countries to benefit from carbon payments for preservation of threatened carbon stocks.

Global Climate Change - The Power Generation Challenge

EPA Science Inventory

The planet continues to warm; O.5 C from the 1970’s to the 2000’s. Also, worldwide CO2 emissions have increased at a 3% annual growth rate from 2000 to 2010. Such emissions are driven by fossil fuel combustion, especially in the power generation sector, & especial...

40 CFR 98.333 - Calculating GHG emissions.

Code of Federal Regulations, 2011 CFR

2011-07-01

... (CONTINUED) MANDATORY GREENHOUSE GAS REPORTING Zinc Production § 98.333 Calculating GHG emissions. You must... your facility used for zinc production, you must determine the mass of carbon in each carbon-containing... weights, CO2 to carbon. 2000/2205 = Conversion factor to convert tons to metric tons. (Zinc)k = Annual...

40 CFR Appendix to Subpart Eee of... - Quality Assurance Procedures for Continuous Emissions Monitors Used for Hazardous Waste Combustors

Code of Federal Regulations, 2012 CFR

2012-07-01

... capabilities. 2.2Relative Accuracy (RA). The absolute mean difference between the pollutant concentration... adjustment took place. 2.4Zero Drift (ZD). The difference in CEMS output readings at the zero pollutant level... Evaluation for CO, O2, and HC CEMS Carbon Monoxide (CO), Oxygen (O2), and Hydrocarbon (HC) CEMS. An Absolute...

40 CFR Appendix to Subpart Eee of... - Quality Assurance Procedures for Continuous Emissions Monitors Used for Hazardous Waste Combustors

Code of Federal Regulations, 2011 CFR

2011-07-01

... capabilities. 2.2Relative Accuracy (RA). The absolute mean difference between the pollutant concentration... adjustment took place. 2.4Zero Drift (ZD). The difference in CEMS output readings at the zero pollutant level... Evaluation for CO, O2, and HC CEMS Carbon Monoxide (CO), Oxygen (O2), and Hydrocarbon (HC) CEMS. An Absolute...

Estimation of the fossil fuel component in atmospheric CO2 based on radiocarbon measurements at the Beromünster tall tower, Switzerland

NASA Astrophysics Data System (ADS)

Berhanu, Tesfaye A.; Szidat, Sönke; Brunner, Dominik; Satar, Ece; Schanda, Rüdiger; Nyfeler, Peter; Battaglia, Michael; Steinbacher, Martin; Hammer, Samuel; Leuenberger, Markus

2017-09-01

Fossil fuel CO2 (CO2ff) is the major contributor of anthropogenic CO2 in the atmosphere, and accurate quantification is essential to better understand the carbon cycle. Since October 2012, we have been continuously measuring the mixing ratios of CO, CO2, CH4, and H2O at five different heights at the Beromünster tall tower, Switzerland. Air samples for radiocarbon (Δ14CO2) analysis have also been collected from the highest sampling inlet (212.5 m) of the tower on a biweekly basis. A correction was applied for 14CO2 emissions from nearby nuclear power plants (NPPs), which have been simulated with the Lagrangian transport model FLEXPART-COSMO. The 14CO2 emissions from NPPs offset the depletion in 14C by fossil fuel emissions, resulting in an underestimation of the fossil fuel component in atmospheric CO2 by about 16 %. An average observed ratio (RCO) of 13.4 ± 1.3 mmol mol-1 was calculated from the enhancements in CO mixing ratios relative to the clean-air reference site Jungfraujoch (ΔCO) and the radiocarbon-based fossil fuel CO2 mole fractions. The wintertime RCO estimate of 12.5 ± 3.3 is about 30 % higher than the wintertime ratio between in situ measured CO and CO2 enhancements at Beromünster over the Jungfraujoch background (8.7 mmol mol-1) corrected for non-fossil contributions due to strong biospheric contribution despite the strong correlation between ΔCO and ΔCO2 in winter. By combining the ratio derived using the radiocarbon measurements and the in situ measured CO mixing ratios, a high-resolution time series of CO2ff was calculated exhibiting a clear seasonality driven by seasonal variability in emissions and vertical mixing. By subtracting the fossil fuel component and the large-scale background, we have determined the regional biospheric CO2 component that is characterized by seasonal variations ranging between -15 and +30 ppm. A pronounced diurnal variation was observed during summer modulated by biospheric exchange and vertical mixing, while no consistent pattern was found during winter.

Urban Greenhouse Gas Emissions Monitoring in Davos, Switzerland, Before, During and After the World Economic Forum Annual Meeting 2012

NASA Astrophysics Data System (ADS)

Jacobson, Gloria; Davis, Ken; Richardson, Scott; Miles, Natasha; Lauvaux, Thomas; Deng, Aijun; Calonder, Gian-Paul; Ruesch, Marc; Lehning, Michael; Bals, Andre; DeCola, Phil; Rella, Chris

2013-04-01

Efforts to reduce anthropogenic greenhouse gas emissions require validation. Atmospheric measurements capture all emissions, and provide a unique and powerful means of continuous validation and feedback. To demonstrate the utility of real time greenhouse gas measurements, in-situ GHG mixing ratio instruments were deployed in Davos, Switzerland to measure emissions from the city before, during and after the World Economic Forum (WEF). Three Instruments were deployed at two separate locations over 3 months (late December 2011 to February 2012). One site was located in the middle of the Davos urban area and a second site was located out of the valley in the surrounding mountains. Carbon Dioxide (CO2), Methane (CH4), Carbon Monoxide (CO) and water vapor (H2O) were measured continuously by Picarro G2401 instruments at both sites. Additionally, a Picarro flux analyzer was deployed in the city to evaluate the inverse fluxes. The mesoscale atmospheric model, WRF nudged to meteorological observations (WRF-FDDA), was used to simulate the transport of GHG over the valley of Davos at 1.3km resolution. A Mini Micro Pulse LiDAR (MiniMPL) from Sigma Space was deployed to evaluate the simulated planetary boundary layer depth from the WRF-FDDA model. The initial flux estimates for CO2 were constructed based on inventories reported for 2005. CO2 mixing ratio measurements prior to WEF suggest the difference between modeled (real-time) and inventory (annual) emissions to be on the order of +40%. The enhancement is likely due to the increased use of heating fuel in the winter. We present here the temporal variability in the inverse fluxes, which are correlated with a cold wave severely affecting Western Europe during the past winter, as well as changes in anthropogenic activities during the week of the WEF meeting. Also presented are new analyses of composite diurnal cycles of hourly CO/CO2 ratios, which provide additional information on the contributions of traffic relative to heating fuel. The absence of traffic peaks during the WEF meeting, indicate a change in road emissions potentially responsible for the observed decrease in the city emissions during the meeting. Acknowledgments: Calibration tanks were provided by C. Sweeney, NOAA ESRL.

Recent observations of carbon and sulfur gas emissions from Tavurvur, Bagana and Ulawun (Papua New Guinea) with a combination of ground- and air-borne direct and remote sensing techniques

NASA Astrophysics Data System (ADS)

Arellano, Santiago; Galle, Bo; Mulina, Kila; Wallius, Julia; McCormick, Brendan; Salem, Lois; D'aleo, Roberto; Itikarai, Ima; Tirpitz, Lukas; Bobrowski, Nicole; Aiuppa, Alessandro

2017-04-01

Satellite observations reveal that volcanoes from Papua New Guinea contributed with ca. 15{%} of the global emission of volcanic sulfur dioxide (SO2) during the period 2005-2014. Relatively little is known about their carbon dioxide (CO2) outputs and more recent levels and dynamics of degassing activity. During September 2016 we conducted measurements of the CO2/SO2 ratio and the SO2 flux from Tavurvur, Bagana and Ulawun volcanoes using a combination of remote sensing and direct sampling techniques. Tavurvur exhibits low-level passive degassing from a modestly active vent and few other intra-crater fumaroles, which made access possible for direct measurements of the CO2/SO2 ratio with a compact Multi-GAS instrument. A wide-field of view pointing DOAS monitor was deployed for longer term monitoring of the SO2 flux from a distance of about 2 km. Bagana degasses continuously with occasional emissions of ash, and its SO2 flux, plume velocity and height was constrained by simultaneous scanning and dual-beam DOAS measurements. Molar ratios in the plume of Bagana were measured by the compact Multi-GAS aboard a multi-rotor UAV, up to a height of 1.6 km above ground. Ulawun showed continuous passive degassing and measurements with the UAV, up to an altitude of ca. 1.8 km, and mobile-DOAS traverses from a car were used to constrain its gas emission. Here we present an overview of the challenging conditions, measurement strategies and results of this campaign that forms part of the ongoing international effort DECADE aiming to better quantify the global gas emission of carbon- and sulfur containing species from volcanoes.

Measurement of black carbon emissions from in-use diesel-electric passenger locomotives in California

NASA Astrophysics Data System (ADS)

Tang, N. W.; Kirchstetter, T.; Martien, P. T.; Apte, J.

2015-12-01

Black carbon (BC) emission factors were measured for a California commuter rail line fleet of diesel-electric passenger locomotives (Caltrain). The emission factors are based on BC and carbon dioxide (CO2) concentrations in the exhaust plumes of passing locomotives, which were measured from pedestrian overpasses using portable analyzers. Each of the 29 locomotives in the fleet was sampled on 4-20 separate occasions at different locations to characterize different driving modes. The average emission factor expressed as g BC emitted per kg diesel consumed was 0.87 ± 0.66 g kg-1 (±1 standard deviation, n = 362 samples). BC emission factors tended to be higher for accelerating locomotives traveling at higher speeds with engines in higher notch settings. Higher fuel-based BC emission factors (g kg-1) were measured for locomotives equipped with separate "head-end" power generators (SEP-HEPs), which power the passenger cars, while higher time-based emission factors (g h-1) were measured for locomotives without SEP-HEPs, whose engines are continuously operated at high speeds to provide both head-end and propulsion power. PM10 emission factors, estimated assuming a BC/PM10 emission ratio of 0.6 and a typical power output-to-fuel consumption ratio, were generally in line with the Environmental Protection Agency's locomotive exhaust emission standards. Per passenger mile, diesel-electric locomotives in this study emit only 20% of the CO2 emitted by typical gasoline-powered light-duty vehicles (i.e., cars). However, the reduction in carbon footprint (expressed in terms of CO2 equivalents) due to CO2 emissions avoidance from a passenger commuting by train rather than car is appreciably offset by the locomotive's higher BC emissions.

Measurement of black carbon emissions from in-use diesel-electric passenger locomotives in California

NASA Astrophysics Data System (ADS)

Tang, Nicholas W.; Apte, Joshua S.; Martien, Philip T.; Kirchstetter, Thomas W.

2015-08-01

Black carbon (BC) emission factors were measured for a California commuter rail line fleet of diesel-electric passenger locomotives (Caltrain). The emission factors are based on BC and carbon dioxide (CO2) concentrations in the exhaust plumes of passing locomotives, which were measured from pedestrian overpasses using portable analyzers. Each of the 29 locomotives in the fleet was sampled on 4-20 separate occasions at different locations to characterize different driving modes. The average emission factor expressed as g BC emitted per kg diesel consumed was 0.87 ± 0.66 g kg-1 (±1 standard deviation, n = 362 samples). BC emission factors tended to be higher for accelerating locomotives traveling at higher speeds with engines in higher notch settings. Higher fuel-based BC emission factors (g kg-1) were measured for locomotives equipped with separate ;head-end; power generators (SEP-HEPs), which power the passenger cars, while higher time-based emission factors (g h-1) were measured for locomotives without SEP-HEPs, whose engines are continuously operated at high speeds to provide both head-end and propulsion power. PM10 emission factors, estimated assuming a BC/PM10 emission ratio of 0.6 and a typical power output-to-fuel consumption ratio, were generally in line with the Environmental Protection Agency's locomotive exhaust emission standards. Per passenger mile, diesel-electric locomotives in this study emit only 20% of the CO2 emitted by typical gasoline-powered light-duty vehicles (i.e., cars). However, the reduction in carbon footprint (expressed in terms of CO2 equivalents) due to CO2 emissions avoidance from a passenger commuting by train rather than car is appreciably offset by the locomotive's higher BC emissions.

The Climate Science Special Report: Perspectives on Climate Change Mitigation

NASA Astrophysics Data System (ADS)

DeAngelo, B. J.

2017-12-01

This chapter of CSSR provides scientific context for key issues regarding the long-term mitigation of climate change. Policy analysis and recommendations are beyond the scope of CSSR. Limiting and stabilizing warming to any level implies that there is an upper limit to the cumulative amount of CO2 that can be added to the atmosphere. Eventually stabilizing the global temperature requires CO2 emissions to approach zero. For a 3.6°F (2°C) or any desired global mean temperature target, an estimated range of allowable cumulative CO2 emissions from the current period onward can be calculated. Accounting for the temperature effects of non-CO2 species, cumulative CO2 emissions are required to stay below about 800 GtC in order to provide a two-thirds likelihood of preventing 3.6°F (2°C) of warming, meaning approximately 230 GtC more could be emitted globally. Assuming global emissions follow the range between the RCP8.5 and RCP4.5 scenarios, emissions could continue for approximately two decades before this cumulative carbon threshold is exceeded. Meeting a 2.7°F (1.5°C) target implies much tighter constraints. Mitigation of non-CO2 species contributes substantially to near-term cooling benefits but cannot be relied upon for ultimate stabilization goals. Successful implementation of the first round of Nationally Determined Contributions associated with the Paris Agreement will provide some likelihood of meeting the long-term temperature goal of limiting global warming to "well below" 3.6°F (2°C) above preindustrial levels; the likelihood depends strongly on the magnitude of global emission reductions after 2030. If interest in geoengineering increases, interest will also increase in assessments of the technical feasibilities, costs, risks, co-benefits, and governance challenges of these additional measures, which are as yet unproven at scale.

40 CFR 86.318-79 - Oxides of nitrogen analyzer specifications.

Code of Federal Regulations, 2010 CFR

2010-07-01

...) AIR PROGRAMS (CONTINUED) CONTROL OF EMISSIONS FROM NEW AND IN-USE HIGHWAY VEHICLES AND ENGINES... be calibrated per § 86.330. (5) The minimum water rejection ratio (maximum water interference) for the NO NDIR analyzer shall be 5,000:1 (see § 86.321). (6) The minimum CO2 rejection ratio (maximum CO2...

Volcanic soil gas 4He/CO2 ratio: a useful geochemical tool for eruption forecasting

NASA Astrophysics Data System (ADS)

Asensio-Ramos, M.; Perez, N. M.; Padron, E.; Melián, G.; Hernandez Perez, P. A.; Padilla, G.; Barrancos, J.; Rodríguez, F.; Sumino, H.; Calvo, D.

2016-12-01

Magmatic gases that percolate through volcano's porous flanks in a non-visible (diffuse) way disturb the chemical composition of soil gases at the surface environment of the volcano, generating enrichments of CO2, He and other gases. Two of the gases which have attracted attention in soil degassing studies are He and CO2 because both species have similar low solubility in silicate melts. However, once they are exsolved from the melts, their movement through the crust towards the surface is very different: CO2, which is a reactive gas, is affected by the occurrence of interfering processes, while interaction of He during its ascent is minimum. Their geochemical differences yield higher relative He/CO2 ratios in the fumarole gases than is actually present in the magma, but it decreases when the magma reservoir reaches enough pressure to generate incipient fracture systems approaching the eruption. In this work, we present quasi daily estimations of diffusive He through the whole surface of El Hierro, the youngest island of the Canarian archipelago, considering He emission data reported in the literature (Padrón et al., 2013. Geology, 41, 539-542), using the same procedure as for diffuse CO2 emission time series (Melián et al., 2014. J. Geophys. Res., 119, 6976-6991). After the occurrence of more than 11,000 seismic events, a shallow submarine eruption about 2 km off the south coast in the southernmost part of El Hierro, started in October 12, 2011 and lasted for 5 month. The herein presented methodology enables the calculation of the diffuse He/CO2 emission ratio of the entire island during the volcanic unrest. Two different emission peaks for both He and CO2, with approximately the same delay between them ( 23 days), were observed. The combination of both time series resulted in a drastic increase in the He/CO2 emission ratio of the island (up to 1.1×10-3) two weeks before the eruption onset. Additionally, a second significant He/CO2 emission peak (up to 5.5×10-4) was observed between 3 and 4 November, some days before the highest lava emission period. The detailed time series of He/CO2 emission ratio during El Hierro 2011-2012 submarine eruption presented here demonstrate the importance of its continuous monitoring in active volcanic regions, mainly in areas without visible manifestations of volcanic fluid discharges.

Influence of disturbance on carbon exchange in a permafrost collapse and adjacent burned forest

USGS Publications Warehouse

Myers-Smith, I. H.; McGuire, A.D.; Harden, J.W.; Chapin, F. S.

2007-01-01

We measured CO2 and CH4 exchange from the center of a Sphagnum-dominated permafrost collapse, through an aquatic most, and into a recently burned black spruce forest on the Tanana River floodplain in interior Alaska. In the anomalously dry growing season of 2004, both the collapse and the surrounding burned area were net sink, s for CO2, with a mean daytime net ecosystem exchange of -1.4 ??mol CO2 m-2 s-1, while the moat was a CH4 source with a mean flux of 0.013 ??mol CH4 m-2 s-1. Regression analyses identified temperature as the dominant factor affecting intragrowing season variation in CO2 exchange and soil moisture as the primary control influencing CH4 emissions. CH4 emissions during the wettest portion of the growing season were four times higher than during the driest periods. If temperatures continue to warm, peatlahd vegetation will likely expand with permafrost degradation, resulting in greater carbon accumulation and methane emissions for the landscape as a whole. Copyright 2007 by the American Geophysical Union.

Ocean Carbon Cycle Feedbacks Under Negative Emissions

NASA Astrophysics Data System (ADS)

Schwinger, Jörg; Tjiputra, Jerry

2018-05-01

Negative emissions will most likely be needed to achieve ambitious climate targets, such as limiting global warming to 1.5°. Here we analyze the ocean carbon-concentration and carbon-climate feedback in an Earth system model under an idealized strong CO2 peak and decline scenario. We find that the ocean carbon-climate feedback is not reversible by means of negative emissions on decadal to centennial timescales. When preindustrial surface climate is restored, the oceans, due to the carbon-climate feedback, still contain about 110 Pg less carbon compared to a simulation without climate change. This result is unsurprising but highlights an issue with a widely used carbon cycle feedback metric. We show that this metric can be greatly improved by using ocean potential temperature as a proxy for climate change. The nonlinearity (nonadditivity) of climate and CO2-driven feedbacks continues to grow after the atmospheric CO2 peak.

Assessing Greenhouse Gas emissions in the Greater Toronto Area using atmospheric observations (Invited)

NASA Astrophysics Data System (ADS)

Vogel, F. R.; Chan, E.; Huang, L.; Levin, I.; Worthy, D.

2013-12-01

Urban areas are said to be responsible for approximately 75% of anthropogenic Greenhouse Gases (GHGs) emissions while comprising only two percent of the land area [1]. This limited spatial expansion should facilitate a monitoring of anthropogenic GHGs from atmospheric observations. As major sources of emissions, cities also have a huge potential to drive emissions reductions. To effectively manage emissions, cities must however, first measure and report these publicly [2]. Modelling studies and measurements of CO2 from fossil fuel burning (FFCO2) in densely populated areas does, however, pose several challenges: Besides continuous in-situ observations, i.e. finding an adequate atmospheric transport model, a sufficiently fine-grained FFCO2 emission model and the proper background reference observations to distinguish the large-scale from the local/urban contributions to the observed FFCO2 concentration offsets ( ΔFFCO2) are required. Pilot studies which include the data from two 'sister sites*' in the vicinity of Toronto, Canada helped to derive flux estimates for Non-CO2 GHGs [3] and improve our understanding of urban FFCO2 emissions. Our 13CO2 observations reveal that the contribution of natural gas burning (mostly due to domestic heating) account for 80%×7% of FFCO2 emissions in the Greater Toronto Area (GTA) during winter. Our 14CO2 observations in the GTA, furthermore, show that the local offset of CO2 (ΔCO2) between our two sister sites can be largely attributed to urban FFCO2 emissions. The seasonal cycle of the observed ΔFFCO2 in Toronto, combined with high-resolution atmospheric modeling, helps to independently assess the contribution from different emission sectors (transportation, primary energy and industry, domestic heating) as predicted by a dedicated city-scale emission inventory, which deviates from a UNFCCC-based inventory. [1] D. Dodman. 2009. Blaming cities for climate change? An analysis of urban greenhouse gas emissions inventories. Environment and Urbanization, 21,185. [2] Arikan Y., Desaim R., Bhatia P. and W. K. Fong, 2012 Global Protocol for Community-Scale Greenhouse Gas Emissions (GPC), C40 Cities Climate Leadership group, available at: http://www.c40.org [3] Vogel, F. R., Ishizawa, M., Chan, E., Chan, D., Hammer, S., Levin, I., & Worthy, D. E. J. (2012). Regional non-CO2 greenhouse gas fluxes inferred from atmospheric measurements in Ontario, Canada. Journal of Integrative Environmental Sciences, 9(1), 41-55. *The term 'sister sites' refers to sites that share a common background signal (i.e. common large scale influence), while significantly differing sensitivities to urban GHG emissions. In our case: Egbert, Ontario and Downsview, Toronto, Ontario.

On-road vehicle emission control in Beijing: past, present, and future.

PubMed

Wu, Ye; Wang, Renjie; Zhou, Yu; Lin, Bohong; Fu, Lixin; He, Kebin; Hao, Jiming

2011-01-01

Beijing, the capital of China, has experienced rapid motorization since 1990; a trend that is likely to continue. The growth in vehicles and the corresponding emissions create challenges to improving the urban air quality. In an effort to reduce the impact of vehicle emissions on urban air quality, Beijing has adopted a number of vehicle emission control strategies and policies since the mid 1990 s. These are classified into seven categories: (1) emission control on new vehicles; (2) emission control on in-use vehicles; (3) fuel quality improvements; (4) alternative-fuel and advanced vehicles; (5) economic policies; (6) public transport; and (7) temporal traffic control measures. Many have proven to be successful, such as the Euro emission standards, unleaded gasoline and low sulfur fuel, temporal traffic control measures during the Beijing Olympic Games, etc. Some, however, have been failures, such as the gasoline-to-LPG taxi retrofit program. Thanks to the emission standards for new vehicles as well as other controls, the fleet-average emission rates of CO, HC, NO(X), and PM(10) by each major vehicle category are decreasing over time. For example, gasoline cars decreased fleet-average emission factors by 12.5% for CO, 10.0% for HC, 5.8% for NO(X), and 13.0% for PM(10) annually since 1995, and such a trend is likely to continue. Total emissions for Beijing's vehicle fleet increased from 1995 to 1998. However, they show a clear and steady decrease between 1999 and 2009. In 2009, total emissions of CO, HC, NO(X), and PM(10) were 845,000 t, 121,000 t, 84,000 t, and 3700 t, respectively; with reductions of 47%, 49%, 47%, and 42%, relative to 1998. Beijing has been considered a pioneer in controlling vehicle emissions within China, similar to the role of California to the U.S. The continued rapid growth of vehicles, however, is challenging Beijing's policy-makers.

Temperature dependence of greenhouse gas emissions from three hydromorphic soils at different groundwater levels.

PubMed

Vicca, S; Janssens, I A; Flessa, H; Fiedler, S; Jungkunst, H F

2009-09-01

Wetlands contribute considerably to the global greenhouse gas (GHG) balance. In these ecosystems, groundwater level (GWL) and temperature, two factors likely to be altered by climate change, exert important control over CO(2), CH(4) and N(2)O fluxes. However, little is known about the temperature sensitivity (Q(10)) of the combined GHG emissions from hydromorphic soils and how this Q(10) varies with GWL. We performed a greenhouse experiment in which three different (plant-free) hydromorphic soils from a temperate spruce forest were exposed to two GWLs (an intermediate GWL of -20 cm and a high GWL of -5 cm). Net CO(2), CH(4) and N(2)O fluxes were measured continuously. Here, we discuss how these fluxes responded to synoptic temperature fluctuations. Across all soils and GWLs, CO(2) emissions responded similarly to temperature and Q(10) was close to 2. The Q(10) of the CH(4) and N(2)O fluxes also was similar across soil types. GWL, on the other hand, significantly affected the Q(10) of both CH(4) and N(2)O emissions. The Q(10) of the net CH(4) fluxes increased from about 1 at GWL = -20 cm to 3 at GWL = -5 cm. For the N(2)O emissions, Q(10) varied around 2 for GWL = -20 cm and around 4 for GWL = -5 cm. This substantial GWL-effect on the Q(10) of CH(4) and N(2)O emissions was, however, hardly reflected in the Q(10) of the total GHG emissions (which varied around 2), because the contribution of these gases was relatively small compared to that of CO(2).

Does the high–tech industry consistently reduce CO{sub 2} emissions? Results from nonparametric additive regression model

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

Xu, Bin; Research Center of Applied Statistics, Jiangxi University of Finance and Economics, Nanchang, Jiangxi 330013; Lin, Boqiang, E-mail: bqlin@xmu.edu.cn

China is currently the world's largest carbon dioxide (CO{sub 2}) emitter. Moreover, total energy consumption and CO{sub 2} emissions in China will continue to increase due to the rapid growth of industrialization and urbanization. Therefore, vigorously developing the high–tech industry becomes an inevitable choice to reduce CO{sub 2} emissions at the moment or in the future. However, ignoring the existing nonlinear links between economic variables, most scholars use traditional linear models to explore the impact of the high–tech industry on CO{sub 2} emissions from an aggregate perspective. Few studies have focused on nonlinear relationships and regional differences in China. Basedmore » on panel data of 1998–2014, this study uses the nonparametric additive regression model to explore the nonlinear effect of the high–tech industry from a regional perspective. The estimated results show that the residual sum of squares (SSR) of the nonparametric additive regression model in the eastern, central and western regions are 0.693, 0.054 and 0.085 respectively, which are much less those that of the traditional linear regression model (3.158, 4.227 and 7.196). This verifies that the nonparametric additive regression model has a better fitting effect. Specifically, the high–tech industry produces an inverted “U–shaped” nonlinear impact on CO{sub 2} emissions in the eastern region, but a positive “U–shaped” nonlinear effect in the central and western regions. Therefore, the nonlinear impact of the high–tech industry on CO{sub 2} emissions in the three regions should be given adequate attention in developing effective abatement policies. - Highlights: • The nonlinear effect of the high–tech industry on CO{sub 2} emissions was investigated. • The high–tech industry yields an inverted “U–shaped” effect in the eastern region. • The high–tech industry has a positive “U–shaped” nonlinear effect in other regions. • The linear impact of the high–tech industry in the eastern region is the strongest.« less

Automated CO2, CH4 and N2O Fluxes from Tree Stems and Soils: Magnitudes, Temporal Patterns and Drivers

NASA Astrophysics Data System (ADS)

Barba, J.; Poyatos, R.; Vargas, R.

2017-12-01

The emissions of the main greenhouse gases (GHG; CO2, CH4 and N2O) through tree stems are still an uncertain component of the total GHG balance of forests. Despite that stem CO2 emissions have been studied for several decades, it is still unclear the drivers and spatiotemporal patterns of CH4 and N2O stem emissions. Additionally, it is unknown how stem emissions could be related to soil physiological processes or environmental conditions. We measured CO2, CH4 and N2O emissions hourly from April to July 2017 at two different heights (75 [LStem] and 150cm [HStem]) of bitternut hickory (Carya cordiformis) trees and adjacent soil locations in a forested area in the Mid Atlantic of the USA. We designed an automated system to continuously measure the three greenhouse gases (GHG) in stems and soils. Stem and soil CO2 emissions showed similar seasonal patterns with an average of 6.56±0.09 (soil), 3.72±0.05 (LStem) and 2.47±0.04 µmols m-2 s-1 (HStem) (mean±95% CI). Soil temperature controlled CO2 fluxes at both daily and seasonal scales (R2>0.5 for all cases), but there was no clear effect of soil moisture. The stems were a clear CH4 source with emissions decreasing with height (0.35±0.02 and 0.25±0.01 nmols m-2 s-1 for LStem and HStem, respectively) with no apparent seasonal pattern, and no clear relationship with environmental drivers (e.g., temperature, moisture). In contrast, soil was a CH4 sink throughout the experiment (-0.55±0.02 nmols m-2 s-1) and its seasonal pattern responded to moisture changes. Despite soil and stem N2O emissions did not show a seasonal pattern or apparent dependency on temperature or moisture, they showed net N2O emissions with a decrease in emissions with stem height (0.29±0.05 for soil, 0.38±0.06 for LStem and 0.28±0.05 nmols m-2 s-1 for HStem). The three GHG emissions decreased with stem height at similar rates (33%, 28% and 27% for CO2, CH4 and N2O, respectively). These results suggest that the gases were not produced in the stem but originated in the soil and transported within the stem. At the forest stand level, the CH4 sink capacity of soils could be partially counteracted by the stem emissions. These results indicate the need to measure CO2, CH4 and N2O emissions not only in soil but also in stems to account for the total GHG balance in ecosystems.

Soil pH management without lime, a strategy to reduce greenhouse gas emissions from cultivated soils

NASA Astrophysics Data System (ADS)

Nadeem, Shahid; Bakken, Lars; Reent Köster, Jan; Tore Mørkved, Pål; Simon, Nina; Dörsch, Peter

2015-04-01

For decades, agricultural scientists have searched for methods to reduce the climate forcing of food production by increasing carbon sequestration in the soil and reducing the emissions of nitrous oxide (N2O). The outcome of this research is depressingly meagre and the two targets appear incompatible: efforts to increase carbon sequestration appear to enhance the emissions of N2O. Currently there is a need to find alternative management strategies which may effectively reduce both the CO2 and N2O footprints of food production. Soil pH is a master variable in soil productivity and plays an important role in controlling the chemical and biological activity in soil. Recent investigations of the physiology of denitrification have provided compelling evidence that the emission of N2O declines with increasing pH within the range 5-7. Thus, by managing the soil pH at a near neutral level appears to be a feasible way to reduce N2O emissions. Such pH management has been a target in conventional agriculture for a long time, since a near-neutral pH is optimal for a majority of cultivated plants. The traditional way to counteract acidification of agricultural soils is to apply lime, which inevitably leads to emission of CO2. An alternative way to increase the soil pH is the use of mafic rock powders, which have been shown to counteract soil acidification, albeit with a slower reaction than lime. Here we report a newly established field trail in Norway, in which we compare the effects of lime and different mafic mineral and rock powders (olivine, different types of plagioclase) on CO2 and N2O emissions under natural agricultural conditions. Soil pH is measured on a monthly basis from all treatment plots. Greenhouse gas (GHG) emission measurements are carried out on a weekly basis using static chambers and an autonomous robot using fast box technique. Field results from the first winter (fallow) show immediate effect of lime on soil pH, and slower effects of the mafic rocks. The plots with mafic rock powders have lower CO2 and N2O emissions as compared with calcite and dolomite. The experiment will be continued for several years under conventionally managed continuous grass, and is unique in its kind allowing to compare different strategies for pH management on GHG emissions.

Improving the City-scale Emission Inventory of Anthropogenic Air Pollutants: A Case Study of Nanjing

NASA Astrophysics Data System (ADS)

Qiu, L.; Zhao, Y.; Xu, R.; Xie, F.; Wang, H.; Qin, H.; Wu, X.; Zhang, J.

2014-12-01

To evaluate the improvement of city-scale emission inventory, a high-resolution emission inventory of air pollutants for Nanjing is first developed combining detailed source information, and then justified through quantitative analysis with observations. The best available domestic emission factors and unit-/facility-based activity level data were compiled based on a thorough field survey on major emission sources. Totally 1089 individual emission sources were identified as point sources and all the emission-related parameters including burner type, combustion technology, fuel quality, and removal efficiency of pollution control devices, are carefully investigated and analyzed. Some new data such as detailed information of city fueling-gas stations, construction sites, monthly activity level, data from continuous emission monitoring systems and traffic flow information were combined to improve spatiotemporal distribution of this inventory. For SO2, NOX and CO, good spatial correlations were found between ground observation (9 state controlling air sampling sites in Nanjing) and city-scale emission inventory (R2=0.34, 0.38 and 0.74, respectively). For TSP, PM10 and PM2.5, however, poorer correlation was found due to relatively weaker accuracy in emission estimation and spatial distribution of road dust. The mixing ratios between specific pollutants including OC/EC, BC/CO and CO2/CO, are well correlated between those from ground observation and emission. Compared to MEIC (Multi-resolution Emission Inventory for China), there is a better spatial consistence between this city-scale emission inventory and NO2 measured by OMI (Ozone Monitoring Instrument). In particular, the city-scale emission inventory still correlated well with satellite observations (R2=0.28) while the regional emission inventory showed little correlation with satellite observations (R2=0.09) when grids containing power plants are excluded. It thus confirms the improvement of city-scale emission inventory on industrial and transportation sources other than big power plants. Through the inventory evaluation, the necessity to develop high-resolution emission inventory with comprehensive emission source information is revealed for atmospheric science studies and air quality improvement at local scale.

Mitigation potential of soil carbon management overestimated by neglecting N2O emissions

NASA Astrophysics Data System (ADS)

Lugato, Emanuele; Leip, Adrian; Jones, Arwyn

2018-03-01

International initiatives such as the `4 per 1000' are promoting enhanced carbon (C) sequestration in agricultural soils as a way to mitigate greenhouse gas emissions1. However, changes in soil organic C turnover feed back into the nitrogen (N) cycle2, meaning that variation in soil nitrous oxide (N2O) emissions may offset or enhance C sequestration actions3. Here we use a biogeochemistry model on approximately 8,000 soil sampling locations in the European Union4 to quantify the net CO2 equivalent (CO2e) fluxes associated with representative C-mitigating agricultural practices. Practices based on integrated crop residue retention and lower soil disturbance are found to not increase N2O emissions as long as C accumulation continues (until around 2040), thereafter leading to a moderate C sequestration offset mostly below 47% by 2100. The introduction of N-fixing cover crops allowed higher C accumulation over the initial 20 years, but this gain was progressively offset by higher N2O emissions over time. By 2060, around half of the sites became a net source of greenhouse gases. We conclude that significant CO2 mitigation can be achieved in the initial 20-30 years of any C management scheme, but after that N inputs should be controlled through appropriate management.

Portable Laser Spectrometer for Airborne and Ground-Based Remote Sensing of Geological CO2 Emissions

NASA Technical Reports Server (NTRS)

Queisser, Manuel; Burton, Mike; Allan, Graham R.; Chiarugi, Antonio

2017-01-01

A 24 kilogram, suitcase-sized, CW (Continuous Wave) Laser Remote Sensing Spectrometer (LARSS) with an approximately 2-kilometer range has been developed. It has demonstrated its flexibility in measuring both atmospheric CO2 from an airborne platform and terrestrial emission of CO2 from a remote mud volcano, Bledug Kuwu, Indonesia, from a ground-based sight. This system scans the CO2 absorption line with 20 discrete wavelengths, as opposed to the typical two-wavelength online-offline instrument. This multi-wavelength approach offers an effective quality control, bias control, and confidence estimate of measured CO2 concentrations via spectral fitting. The simplicity, ruggedness, and flexibility in the design allow for easy transportation and use on different platforms with a quick setup in some of the most challenging climatic conditions. While more refinement is needed, the results represent a stepping stone towards widespread use of active one-sided gas remote sensing in the earth sciences.

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

NASA Astrophysics Data System (ADS)

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

2016-06-01

Cities currently covering only a very small portion ( < 3 %) of the world's land surface directly release to the atmosphere about 44 % of global energy-related CO2, but they are associated with 71-76 % of CO2 emissions from global final energy use. Although many cities have set voluntary climate plans, their CO2 emissions are not evaluated by the monitoring, reporting, and verification (MRV) procedures that play a key role for market- or policy-based mitigation actions. Here we analyze the potential of a monitoring tool that could support the development of such procedures at the city scale. It is based on an atmospheric inversion method that exploits inventory data and continuous atmospheric CO2 concentration measurements from a network of stations within and around cities to estimate city CO2 emissions. This monitoring tool is configured for the quantification of the total and sectoral CO2 emissions in the Paris metropolitan area (˜ 12 million inhabitants and 11.4 TgC emitted in 2010) during the month of January 2011. Its performances are evaluated in terms of uncertainty reduction based on observing system simulation experiments (OSSEs). They are analyzed as a function of the number of sampling sites (measuring at 25 m a.g.l.) and as a function of the network design. The instruments presently used to measure CO2 concentrations at research stations are expensive (typically ˜ EUR 50 k per sensor), which has limited the few current pilot city networks to around 10 sites. Larger theoretical networks are studied here to assess the potential benefit of hypothetical operational lower-cost sensors. The setup of our inversion system is based on a number of diagnostics and assumptions from previous city-scale inversion experiences with real data. We find that, given our assumptions underlying the configuration of the OSSEs, with 10 stations only the uncertainty for the total city CO2 emission during 1 month is significantly reduced by the inversion by ˜ 42 %. It can be further reduced by extending the network, e.g., from 10 to 70 stations, which is promising for MRV applications in the Paris metropolitan area. With 70 stations, the uncertainties in the inverted emissions are reduced significantly over those obtained using 10 stations: by 32 % for commercial and residential buildings, by 33 % for road transport, by 18 % for the production of energy by power plants, and by 31 % for total emissions. These results indicate that such a high number of stations would be likely required for the monitoring of sectoral emissions in Paris using this observation-model framework. They demonstrate some high potential that atmospheric inversions can contribute to the monitoring and/or the verification of city CO2 emissions (baseline) and CO2 emission reductions (commitments) and the advantage that could be brought by the current developments of lower-cost medium precision (LCMP) sensors.

40 CFR 98.232 - GHGs to report.

Code of Federal Regulations, 2014 CFR

2014-07-01

... 40 Protection of Environment 21 2014-07-01 2014-07-01 false GHGs to report. 98.232 Section 98.232 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) MANDATORY GREENHOUSE GAS REPORTING Petroleum and Natural Gas Systems § 98.232 GHGs to report. (a) You must report CO2, CH4, and N2O emissions from each...

40 CFR 98.232 - GHGs to report.

Code of Federal Regulations, 2011 CFR

2011-07-01

... 40 Protection of Environment 21 2011-07-01 2011-07-01 false GHGs to report. 98.232 Section 98.232 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) MANDATORY GREENHOUSE GAS REPORTING Petroleum and Natural Gas Systems § 98.232 GHGs to report. (a) You must report CO2, CH4, and N2O emissions from each...

40 CFR 98.232 - GHGs to report.

Code of Federal Regulations, 2013 CFR

2013-07-01

... 40 Protection of Environment 22 2013-07-01 2013-07-01 false GHGs to report. 98.232 Section 98.232 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) MANDATORY GREENHOUSE GAS REPORTING Petroleum and Natural Gas Systems § 98.232 GHGs to report. (a) You must report CO2, CH4, and N2O emissions from each...

40 CFR 98.232 - GHGs to report.

Code of Federal Regulations, 2012 CFR

2012-07-01

... 40 Protection of Environment 22 2012-07-01 2012-07-01 false GHGs to report. 98.232 Section 98.232 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) MANDATORY GREENHOUSE GAS REPORTING Petroleum and Natural Gas Systems § 98.232 GHGs to report. (a) You must report CO2, CH4, and N2O emissions from each...

Localization of a continuous CO2 leak from an isotropic flat-surface structure using acoustic emission detection and near-field beamforming techniques

NASA Astrophysics Data System (ADS)

Yan, Yong; Cui, Xiwang; Guo, Miao; Han, Xiaojuan

2016-11-01

Seal capacity is of great importance for the safety operation of pressurized vessels. It is crucial to locate the leak hole timely and accurately for reasons of safety and maintenance. This paper presents the principle and application of a linear acoustic emission sensor array and a near-field beamforming technique to identify the location of a continuous CO2 leak from an isotropic flat-surface structure on a pressurized vessel in the carbon capture and storage system. Acoustic signals generated by the leak hole are collected using a linear high-frequency sensor array. Time-frequency analysis and a narrow-band filtering technique are deployed to extract effective information about the leak. The impacts of various factors on the performance of the localization technique are simulated, compared and discussed, including the number of sensors, distance between the leak hole and sensor array and spacing between adjacent sensors. Experiments were carried out on a laboratory-scale test rig to assess the effectiveness and operability of the proposed method. The results obtained suggest that the proposed method is capable of providing accurate and reliable localization of a continuous CO2 leak.

Energy in the Anthropocene

NASA Astrophysics Data System (ADS)

Davis, S. J.; Caldeira, K.; Cao, L.; Hoffert, M.

2012-12-01

Human interference in Earth's natural systems is fueled by ever-increasing consumption of fossil energy. The energy we consume has enabled exponential growth of human population and economic wealth by expanding access to basic goods and services such as food, medicine, light, sanitation and refrigeration, as well as more advanced technologies such as transport and communication. In turn, population growth and economic development drive demand for even more energy. By 2050, it is expected that global energy demand will double to more than 30 TW. Unfortunately, the modern energy system is largely dependent on fossil fuels, and the CO2 released by burning of these fuels is the primary cause of anthropogenic climate change. As human civilization has expanded, primary energy sources have become progressively less carbon intensive, transitioning from the use of unsustainably harvested biomass to coal, oil and then natural gas. However, tremendous growth in the quantity of energy energy consumption in the industrial era has caused rapid growth of CO2 emissions. Limiting these emissions to avoid the more severe impacts of climate change while also meeting future demand for energy will require continuing the process of decarbonization by making a planetary-scale transition to largely carbon-emission-free energy technologies. In 2004, Pacala and Socolow proposed that such a transition could be achieved by stabilizing emissions at then-current levels for 50 years and then decreasing emissions by 2% per year afterward. They divided the task of stabilization into "wedges" that would grow linearly from zero to 1 gigatonne of carbon emissions avoided per year (GtC/y; 1 Gt = 10^12 kg) over 50 years, and asserted that deploying 7 wedges offset the growth of emissions and put us on a trajectory to stabilize atmospheric CO2 concentration at 500 ppm if emissions decreased sharply in the second half of the 21st century. However, in light of the growth of emissions since 2004, new carbon-climate model simulations suggest that stabilizing current emissions for 50 years is no longer consistent with either an atmospheric CO2 concentration of 500 ppm nor global temperature increases below 2°C. Thus, if "solving the carbon-climate problem for the next 50 years" means meeting these climate targets, then solving the climate problem means not just stabilizing but substantially reducing CO2 emissions over the next 50 years, ultimately to near zero. And such large reductions in annual emissions will entail many more than 7 wedges. Depending on whether or not historical rates of decarbonization continue, a phase-out of emissions over 50 years would require between 19 and 31 wedges, beyond the wedges that may already be included in the baseline scenario. This level of mitigation will require affordable carbon-free energy systems to be deployed at the scale of tens of terawatts. Any hope for such fundamental transformation of the global energy system depends upon coordinated efforts to innovate, plan, and deploy new transportation and energy systems that can provide affordable energy at scale without emitting CO2 to the atmosphere. Lacking such efforts, the climate of the Anthropocene will come to resemble that of the Cretaceous.

Diurnal variability of CO2 and CH4 emissions from tropical reservoirs

NASA Astrophysics Data System (ADS)

Linkhorst, Annika; Reinaldo Paranaíba, José; Barros, Nathan; DelSontro, Tonya; Isidorova, Anastasija; Mendonça, Raquel; Sobek, Sebastian

2017-04-01

Reservoirs are important atmospheric sources of carbon dioxide (CO2) and methane (CH4) with CH4 being a greenhouse gas (GHG) at least 28 times more potent than CO2. Reservoir GHG emissions tend to be heterogeneous, however, and thus current emission estimates are likely conservative since they often overlook emission hot spots and hot moments, especially for CH4 ebullition. For CO2, diffusion is the dominant flux pathway, and diurnal patterns in CO2 emissions can largely be linked to photosynthesis. In contrast, ebullition, the release of gases through bubbles that are formed in the sediments and travel through the water column, is a major emission pathway for CH4 in shallow waters. We visually observed a change in quantity and size of bubbles at different times of the day, and therefore conducted a diurnal study in four different Brazilian reservoirs of different size, age, climatic and geographic characteristics. We hypothesized that sub-daily trends in CH4 ebullition occur in Brazilian reservoirs as bubble release depends on physical factors such as turbulence and hydrostatic pressure, which can exhibit sub-daily patterns in large, managed reservoirs. In each reservoir, we performed measurements of CO2 and CH4 fluxes at one location over 24 hours. CH4 ebullition was tracked continuously by an echosounder, and 13 anchored bubble traps per reservoir were sampled every three hours. Further, a custom-built equilibrator monitored dissolved CH4 and CO2 concentrations, and diffusive and total fluxes of CO2 and CH4 were measured using floating chambers in triplicates every 30 minutes during the same period. We observed that CH4 ebullition as well as CH4 and CO2 diffusion peaked during the day, with peak fluxes being up to four times higher than low fluxes. However, the exact timing and magnitude varied for the different sampling events, and could in part be linked to biological and physical properties of the respective reservoir. This study combined different state-of-the-art techniques to show, for the first time, short-scale temporal variability for both diffusion and ebullition of CO2 and CH4 in different tropical reservoirs. It shows substantial and non-negligable diurnal variability in GHG emission from tropical reservoirs. Further studies are needed to find out if the pattern of low flux during night needs to be accounted for in estimations of GHG emission from reservoirs.

CO2 and CH4 exchanges between land ecosystems and the atmosphere in northern high latitudes over the 21st century

USGS Publications Warehouse

Zhuang, Q.; Melillo, J.M.; Sarofim, M.C.; Kicklighter, D.W.; McGuire, A.D.; Felzer, B.S.; Sokolov, A.; Prinn, R.G.; Steudler, P.A.; Hu, S.

2006-01-01

Terrestrial ecosystems of the northern high latitudes (above 50??N) exchange large amounts of CO2 and CH4 with the atmosphere each year. Here we use a process-based model to estimate the budget of CO 2 and CH4 of the region for current climate conditions and for future scenarios by considering effects of permafrost dynamics, CO 2 fertilization of photosynthesis and fire. We find that currently the region is a net source of carbon to the atmosphere at 276 Tg C yr -1. We project that throughout the 21st century, the region will most likely continue as a net source of carbon and the source will increase by up to 473 Tg C yr-1 by the end of the century compared to the current emissions. However our coupled carbon and climate model simulations show that these emissions will exert relatively small radiative forcing on global climate system compared to large amounts of anthropogenic emissions. Copyright 2006 by the American Geophysical Union.

Nitrogen trifluoride global emissions estimated from updated atmospheric measurements

PubMed Central

Arnold, Tim; Harth, Christina M.; Mühle, Jens; Manning, Alistair J.; Salameh, Peter K.; Kim, Jooil; Ivy, Diane J.; Steele, L. Paul; Petrenko, Vasilii V.; Severinghaus, Jeffrey P.; Baggenstos, Daniel; Weiss, Ray F.

2013-01-01

Nitrogen trifluoride (NF3) has potential to make a growing contribution to the Earth’s radiative budget; however, our understanding of its atmospheric burden and emission rates has been limited. Based on a revision of our previous calibration and using an expanded set of atmospheric measurements together with an atmospheric model and inverse method, we estimate that the global emissions of NF3 in 2011 were 1.18 ± 0.21 Gg⋅y−1, or ∼20 Tg CO2-eq⋅y−1 (carbon dioxide equivalent emissions based on a 100-y global warming potential of 16,600 for NF3). The 2011 global mean tropospheric dry air mole fraction was 0.86 ± 0.04 parts per trillion, resulting from an average emissions growth rate of 0.09 Gg⋅y−2 over the prior decade. In terms of CO2 equivalents, current NF3 emissions represent between 17% and 36% of the emissions of other long-lived fluorinated compounds from electronics manufacture. We also estimate that the emissions benefit of using NF3 over hexafluoroethane (C2F6) in electronics manufacture is significant—emissions of between 53 and 220 Tg CO2-eq⋅y−1 were avoided during 2011. Despite these savings, total NF3 emissions, currently ∼10% of production, are still significantly larger than expected assuming global implementation of ideal industrial practices. As such, there is a continuing need for improvements in NF3 emissions reduction strategies to keep pace with its increasing use and to slow its rising contribution to anthropogenic climate forcing. PMID:23341630

Quantifying the relative importance of greenhouse gas emissions from current and future savanna land use change across northern Australia

NASA Astrophysics Data System (ADS)

Bristow, Mila; Hutley, Lindsay B.; Beringer, Jason; Livesley, Stephen J.; Edwards, Andrew C.; Arndt, Stefan K.

2016-11-01

The clearing and burning of tropical savanna leads to globally significant emissions of greenhouse gases (GHGs); however there is large uncertainty relating to the magnitude of this flux. Australia's tropical savannas occupy the northern quarter of the continent, a region of increasing interest for further exploitation of land and water resources. Land use decisions across this vast biome have the potential to influence the national greenhouse gas budget. To better quantify emissions from savanna deforestation and investigate the impact of deforestation on national GHG emissions, we undertook a paired site measurement campaign where emissions were quantified from two tropical savanna woodland sites; one that was deforested and prepared for agricultural land use and a second analogue site that remained uncleared for the duration of a 22-month campaign. At both sites, net ecosystem exchange of CO2 was measured using the eddy covariance method. Observations at the deforested site were continuous before, during and after the clearing event, providing high-resolution data that tracked CO2 emissions through nine phases of land use change. At the deforested site, post-clearing debris was allowed to cure for 6 months and was subsequently burnt, followed by extensive soil preparation for cropping. During the debris burning, fluxes of CO2 as measured by the eddy covariance tower were excluded. For this phase, emissions were estimated by quantifying on-site biomass prior to deforestation and applying savanna-specific emission factors to estimate a fire-derived GHG emission that included both CO2 and non-CO2 gases. The total fuel mass that was consumed during the debris burning was 40.9 Mg C ha-1 and included above- and below-ground woody biomass, course woody debris, twigs, leaf litter and C4 grass fuels. Emissions from the burning were added to the net CO2 fluxes as measured by the eddy covariance tower for other post-deforestation phases to provide a total GHG emission from this land use change. The total emission from this savanna woodland was 148.3 Mg CO2-e ha-1 with the debris burning responsible for 121.9 Mg CO2-e ha-1 or 82 % of the total emission. The remaining emission was attributed to CO2 efflux from soil disturbance during site preparation for agriculture (10 % of the total emission) and decay of debris during the curing period prior to burning (8 %). Over the same period, fluxes at the uncleared savanna woodland site were measured using a second flux tower and over the 22-month observation period, cumulative net ecosystem exchange (NEE) was a net carbon sink of -2.1 Mg C ha-1, or -7.7 Mg CO2-e ha-1. Estimated emissions for this savanna type were then extrapolated to a regional-scale to (1) provide estimates of the magnitude of GHG emissions from any future deforestation and (2) compare them with GHG emissions from prescribed savanna burning that occurs across the northern Australian savanna every year. Emissions from current rate of annual savanna deforestation across northern Australia was double that of reported (non-CO2 only) savanna burning. However, if the total GHG emission, CO2 plus non-CO2 emissions, is accounted for, burning emissions are an order of magnitude larger than that arising from savanna deforestation. We examined a scenario of expanded land use that required additional deforestation of savanna woodlands over and above current rates. This analysis suggested that significant expansion of deforestation area across the northern savanna woodlands could add an additional 3 % to Australia's national GHG account for the duration of the land use change. This bottom-up study provides data that can reduce uncertainty associated with land use change for this extensive tropical ecosystem and provide an assessment of the relative magnitude of GHG emissions from savanna burning and deforestation. Such knowledge can contribute to informing land use decision making processes associated with land and water resource development.

Invisible CO2 gas killing trees at Mammoth Mountain, California

USGS Publications Warehouse

Sorey, Michael L.; Farrar, Christopher D.; Evans, William C.; Hill, David P.; Bailey, Roy A.; Hendley, James W.; Stauffer, Peter H.

1996-01-01

Since 1980, scientists have monitored geologic unrest in Long Valley Caldera and at adjacent Mammoth Mountain, California. After a persistent swarm of earthquakes beneath Mammoth Mountain in 1989, earth scientists discovered that large volumes of carbon dioxide (CO2) gas were seeping from beneath this volcano. This gas is killing trees on the mountain and also can be a danger to people. The USGS continues to study the CO2 emissions to help protect the public from this invisible potential hazard.

Invisible CO2 gas killing trees at Mammoth Mountain, California

USGS Publications Warehouse

Sorey, Michael L.; Farrar, Christopher D.; Gerlach, Terrance M.; McGee, Kenneth A.; Evans, William C.; Colvard, Elizabeth M.; Hill, David P.; Bailey, Roy A.; Rogie, John D.; Hendley, James W.; Stauffer, Peter H.

2000-01-01

Since 1980, scientists have monitored geologic unrest in Long Valley Caldera and at adjacent Mammoth Mountain, California. After a persistent swarm of earthquakes beneath Mammoth Mountain in 1989, geologists discovered that large volumes of carbon dioxide (CO2 ) gas were seeping from beneath this volcano. This gas is killing trees on the mountain and also can be a danger to people. The U.S. Geological Survey (USGS) continues to study the CO2 emissions to help protect the public from this invisible potential hazard.

40 CFR 98.82 - GHGs to report.

Code of Federal Regulations, 2010 CFR

2010-07-01

... 40 Protection of Environment 20 2010-07-01 2010-07-01 false GHGs to report. 98.82 Section 98.82 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) MANDATORY GREENHOUSE GAS REPORTING Cement Production § 98.82 GHGs to report. You must report: (a) CO2 process emissions...

40 CFR 98.82 - GHGs to report.

Code of Federal Regulations, 2011 CFR

2011-07-01

... 40 Protection of Environment 21 2011-07-01 2011-07-01 false GHGs to report. 98.82 Section 98.82 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) MANDATORY GREENHOUSE GAS REPORTING Cement Production § 98.82 GHGs to report. You must report: (a) CO2 process emissions...

HIGH-RESOLUTION CO OBSERVATION OF THE CARBON STAR CIT 6 REVEALING THE SPIRAL STRUCTURE AND A NASCENT BIPOLAR OUTFLOW

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

Kim, Hyosun; Liu, Sheng-Yuan; Hirano, Naomi

2015-11-20

CIT 6 is a carbon star in the transitional phase from the asymptotic giant branch (AGB) to the protoplanetary nebulae (pPNs). Observational evidences of two point sources in the optical, circumstellar arc segments in an HC{sub 3}N line emission, and a bipolar nebula in near-infrared provide strong support for the presence of a binary companion. Hence, CIT 6 is very attractive for studying the role of companions in the AGB–pPN transition. We have carried out high-resolution {sup 12}CO J = 2–1 and {sup 13}CO J = 2–1 observations of CIT 6 with the Submillimeter Array combined with the Submillimeter Telescopemore » (single-dish) data. The {sup 12}CO channel maps reveal a spiral-shell pattern connecting the HC{sub 3}N segments in a continuous form and an asymmetric outflow corresponding to the near-infrared bipolar nebula. Rotation of the {sup 12}CO channel peak position may be related to the inner spiral winding and/or the bipolar outflow. An eccentric orbit binary is suggested for the presence of an anisotropic mass loss to the west and a double spiral pattern. The lack of interarm emission to the west may indicate a feature corresponding to the periastron passage of a highly eccentric orbit of the binary. Spatially averaged radial and spectral profiles of {sup 12}CO J = 2–1 and {sup 13}CO J = 2–1 are compared with simple spherical radiative transfer models, suggesting a change of {sup 12}CO/{sup 13}CO abundance ratio from ∼30 to ∼50 inward in the CSE of CIT 6. The millimeter continuum emission is decomposed into extended dust thermal emission (spectral index ∼ −2.4) and compact emission from radio photosphere (spectral index ∼ −2.0)« less

Modelling global CO2 emissions into the atmosphere from crown, ground, and peat fires

NASA Astrophysics Data System (ADS)

Eliseev, Alexey V.; Mokhov, Igor I.; Chernokulsky, Alexander V.

2015-04-01

The scheme for natural fires implemented in the climate model (CM) developed at the A.M. Obukhov Institute of Atmospheric Physics (IAP RAS) is extended by a module accounting for ground and peat fires. With the IAP RAS CM, the simulations are performed for 1700-2300 in accordance with the CMIP5 (Coupled Models Intercomparison Project, phase 5) protocol. The modelled present-day burnt area, BA, and the corresponding CO2 emissions into the atmosphere E agree with the GFED-3.1 estimates at most regions. In the 21st century, under the RCP (Representative Concentration Pathways) scenarios, the global BA increases by 10-41% depending on scenario, and E increases by 11-39%. Under the mitigation scenario RCP 2.6, both BA and E slightly decrease in the 22nd-23rd centuries. For scenarios RCP 4.5, RCP 6.0, and RCP 8.5, they continue to increase in these two centuries. All these changes are mostly due to changes in natural fires activity in the boreal regions. Ground and peat fires contribute significantly to the total emissions of CO2 from natural fires (20-25% at the global scale depending on scenario and calendar year). Peat fires markedly intensify interannual variability of regional CO2 emissions from natural fires.

Stratospheric ozone depletion due to nitrous oxide: influences of other gases

PubMed Central

Portmann, R. W.; Daniel, J. S.; Ravishankara, A. R.

2012-01-01

The effects of anthropogenic emissions of nitrous oxide (N2O), carbon dioxide (CO2), methane (CH4) and the halocarbons on stratospheric ozone (O3) over the twentieth and twenty-first centuries are isolated using a chemical model of the stratosphere. The future evolution of ozone will depend on each of these gases, with N2O and CO2 probably playing the dominant roles as halocarbons return towards pre-industrial levels. There are nonlinear interactions between these gases that preclude unambiguously separating their effect on ozone. For example, the CH4 increase during the twentieth century reduced the ozone losses owing to halocarbon increases, and the N2O chemical destruction of O3 is buffered by CO2 thermal effects in the middle stratosphere (by approx. 20% for the IPCC A1B/WMO A1 scenario over the time period 1900–2100). Nonetheless, N2O is expected to continue to be the largest anthropogenic emission of an O3-destroying compound in the foreseeable future. Reductions in anthropogenic N2O emissions provide a larger opportunity for reduction in future O3 depletion than any of the remaining uncontrolled halocarbon emissions. It is also shown that 1980 levels of O3 were affected by halocarbons, N2O, CO2 and CH4, and thus may not be a good choice of a benchmark of O3 recovery. PMID:22451111

Biogenic volatile organic compounds (BVOCs) emission of Scots pine under drought stress - a 13CO2 labeling study to determine de novo and pool emissions under different treatments

NASA Astrophysics Data System (ADS)

Lüpke, M.

2015-12-01

Plants emit biogenic volatile organic compounds (BVOCs) to e.g. communicate and to defend herbivores. Yet BVOCs also impact atmospheric chemistry processes, and lead to e.g. the built up of secondary organic aerosols. Abiotic stresses, such as drought, however highly influence plant physiology and subsequently BVOCs emission rates. In this study, we investigated the effect of drought stress on BVOCs emission rates of Scots pine trees, a de novo and pool emitter, under controlled climate chamber conditions within a dynamic enclosure system consisting of four plant chambers. Isotopic labeling with 13CO2 was used to detect which ratio of emissions of BVOCs derives from actual synthesis and from storage organs under different treatments. Additionally, the synthesis rate of the BVOCs synthesis can be determined. The experiment consisted of two campaigns (July 2015 and August 2015) of two control and two treated trees respectively in four controlled dynamic chambers simultaneously. Each campaign lasted for around 21 days and can be split into five phases: adaptation, control, dry-out, drought- and re-watering phase. The actual drought phase lasted around five days. During the campaigns two samples of BVOCs emissions were sampled per day and night on thermal desorption tubes and analyzed by a gas chromatograph coupled with a mass spectrometer and a flame ionization detector. Additionally, gas exchange of water and CO2, soil moisture, as well as leaf and chamber temperature was monitored continuously. 13CO2 labeling was performed simultaneously in all chambers during the phases control, drought and re-watering for five hours respectively. During the 13CO2 labeling four BVOCs emission samples per chamber were taken to identify the labeling rate on emitted BVOCs. First results show a decrease of BVOCs emissions during the drought phase and a recovery of emission after re-watering, as well as different strength of reduction of single compounds. The degree of labeling with 13CO2 differed between the emitted compounds, indicating different sources (pool / de novo) within the plant.

Detecting small scale CO2 emission structures using OCO-2

NASA Astrophysics Data System (ADS)

Schwandner, Florian M.; Eldering, Annmarie; Verhulst, Kristal R.; Miller, Charles E.; Nguyen, Hai M.; Oda, Tomohiro; O'Dell, Christopher; Rao, Preeti; Kahn, Brian; Crisp, David; Gunson, Michael R.; Sanchez, Robert M.; Ashok, Manasa; Pieri, David; Linick, Justin P.; Yuen, Karen

2016-04-01

Localized carbon dioxide (CO2) emission structures cover spatial domains of less than 50 km diameter and include cities and transportation networks, as well as fossil fuel production, upgrading and distribution infra-structure. Anthropogenic sources increasingly upset the natural balance between natural carbon sources and sinks. Mitigation of resulting climate change impacts requires management of emissions, and emissions management requires monitoring, reporting and verification. Space-borne measurements provide a unique opportunity to detect, quantify, and analyze small scale and point source emissions on a global scale. NASA's first satellite dedicated to atmospheric CO2 observation, the July 2014 launched Orbiting Carbon Observatory (OCO-2), now leads the afternoon constellation of satellites (A-Train). Its continuous swath of 2 to 10 km in width and eight footprints across can slice through coincident emission plumes and may provide momentary cross sections. First OCO-2 results demonstrate that we can detect localized source signals in the form of urban total column averaged CO2 enhancements of ~2 ppm against suburban and rural backgrounds. OCO-2's multi-sounding swath observing geometry reveals intra-urban spatial structures reflected in XCO2 data, previously unobserved from space. The transition from single-shot GOSAT soundings detecting urban/rural differences (Kort et al., 2012) to hundreds of soundings per OCO-2 swath opens up the path to future capabilities enabling urban tomography of greenhouse gases. For singular point sources like coal fired power plants, we have developed proxy detections of plumes using bands of imaging spectrometers with sensitivity to SO2 in the thermal infrared (ASTER). This approach provides a means to automate plume detection with subsequent matching and mining of OCO-2 data for enhanced detection efficiency and validation. © California Institute of Technology

The National Emissions Inventory Significantly Overestimates NOx Emissions: Analysis of CMAQ and in situ observations from DISCOVER-AQ

NASA Astrophysics Data System (ADS)

Anderson, D. C.; Dickerson, R. R.; Loughner, C.

2013-12-01

NOx and CO not only adversely impact human health, but they, along with associated VOCs, are also important precursors for O3 formation. While ambient NOx and CO concentrations have decreased dramatically over the past 10-20 years, O3 has remained a more recalcitrant problem, particularly in the Baltimore/Washington region. Reduction of O3 production requires that emissions inventories, such as the National Emissions Inventory (NEI), accurately capture total emissions of CO and NOx while also correctly apportioning them among different sectors. Previous evaluations of the NEI paint different pictures of its accuracy, with assertions that it overestimates either one or both of CO and NOx from anywhere between 25 percent to a factor of 2. These conflicting claims warrant further investigation. In this study, measurements of NOx and CO taken aboard the NOAA P3B airplane during the 2011 DISCOVER-AQ field campaign were used to determine the NOx/CO emissions ratio at 6 locations in the Washington/Baltimore region. An average molar emissions ratio of 12.8 × 1.2 CO/NOx was found by calculating the change in CO over the change in NOx from vertical concentration profiles in the planetary boundary layer. Ratios showed little variation with location. Observed values were approximately a factor of 1.35 - 1.75 times greater than that predicted by the annual, countywide emissions ratio from the 2008 NEI. When compared to a temporalized, gridded version of the inventory processed by SMOKE, ratio observations were greater than that predicted by inventories by up to a factor of 2. Comparison of the in situ measurements and remotely sensed observations from MOPITT of CO to the Community Multiscale Air Quality (CMAQ) model agree within 10-35 percent, with the model higher on average. Measurements of NOy by two separate analytical techniques, on the other hand, show that CMAQ consistently and significantly overestimates NOy concentrations. Combined with the CO observations, this indicates that the NEI overestimates NOx emissions by approximately a factor of 2. Comparison of the temporalized NEI to continuous monitoring of NOx emissions from point sources shows that, on average, agreement between observations and the NEI were within 5 percent. In a region where the NEI estimates on-road emissions can account for 50-75 percent of total NOx, the most likely source of error in the NOx inventory is in the on-road sector. Assumptions about the lifetime and efficacy of catalytic converters in the MOVES model should be investigated as a possible source of this error.

Ammonia and greenhouse gas emissions from a modern U.S. swine breeding-gestation-farrowing system

NASA Astrophysics Data System (ADS)

Stinn, John P.; Xin, Hongwei; Shepherd, Timothy A.; Li, Hong; Burns, Robert T.

2014-12-01

Aerial emissions from livestock production continue to be an area of attention and concern for both the potential health and environmental impacts. However, information of gaseous, especially greenhouse gas (GHG), emissions for swine breeding/gestation and farrowing production systems is limited. The purpose of this study was to quantify ammonia (NH3), carbon dioxide (CO2), nitrous oxide (N2O), and methane (CH4) concentrations and emissions from a modern breeding-gestation-farrowing system located in central Iowa, USA. A 4300-sow farm was selected for the extensive field monitoring which employed a Mobile Air Emission Monitoring Unit equipped with state-of-the-art gas analyzers and a data acquisition system. The monitored portion of the farm facility consisted of a deep-pit breeding/early gestation (B/EG) barn (1800 head), a deep-pit late gestation (LG) barn (1800 head), and two shallow-pit (pull-plug) farrowing rooms (40 head per room). A dynamic flux chamber was used to monitor gaseous emissions from the external manure storage for the farrowing rooms. Data were collected for 29 consecutive months (January 2011 through June 2013). Daily indoor NH3, CO2, N2O, and CH4 concentrations (ppm, mean ± SD) were 12.0 (±7.6), 1594 (±797), 0.31 (±0.11), and 28.5 (±9.8), respectively, in the breeding/gestation barns; and 9.7 (±4.1), 1536 (±701), 0.30 (±0.10), and 78.3 (±37), respectively, in the farrowing rooms. Daily emissions per animal unit (AU, 500 kg live weight) were 35.1 g NH3, 7.46 kg CO2, 0.17 g N2O, and 263.4 g CH4 for sows in the B/EG barn; and 28.2 g NH3, 6.50 kg CO2, 0.12 g N2O, and 201.3 g CH4 for sows in the LG barn. The average daily emissions per AU (sow and piglets) of the farrowing rooms during the lactation period (birth to weaning) were: 59.7 g NH3, 16.4 kg CO2, 0.73 g N2O, and 107 g CH4. For the monitored period, the external manure storage had the following average daily emission per m2 surface area: 1.26 g NH3, 137 g CO2, and 94.8 g CH4, which was equivalent to daily emissions per AU in the farrowing rooms of 12.2 g NH3, 1.055 kg CO2, and 867 g CH4. Average daily emissions per AU for the total operation (including house-level and manure storage emissions) were 38.5 g NH3, 8.73 kg CO2 (including 7.3 kg from animal respiration), 0.25 g N2O, and 301 g CH4.

Gas Phase Emission Ratios From In-Use Diesel and CNG Curbside Passenger Buses in New York City

NASA Astrophysics Data System (ADS)

Herndon, S. C.; Shorter, J.; Canagaratna, M.; Jayne, J.; Nelson, D. D.; Wormhoudt, J. C.; Williams, P.; Silva, P. J.; Shi, Q.; Ghertner, A.; Zahniser, M.; Worsnop, D.; Kolb, C.; Lanni, T.; Drewnick, F.; Demerjian, K. L.

2002-12-01

The Aerodyne Mobile Laboratory simultaneously measured gas phase and particulate emissions from in use vehicles during two campaigns in New York City. The campaigns took place during two weeks in October, 2000 and four weeks in July-August, 2001. Passenger curbside buses were the primary focus of the study, but school buses and several other heavy duty diesel vehicles were also characterized. This paper describes the methodologies used to measure individual in use vehicles and presents the results of the gas phase measurements. Emission ratios for NO, NO2, SO2, N2O, CO, CH4 and H2CO relative to CO2 have been determined across several classes of buses. The gas phase concentrations were measured each second, using Tunable Infrared Laser Direct Absorption Spectroscopy (TILDAS). Some of the categories of buses into which the data has been sorted are; diesel (both 6V92 and Series 50) with and without the Continuous Regenerative Technology (CRT) retrofit, compressed natural gas powered(CNG) and hybrid diesel-electric buses. The New York Metropolitan Transit Authority (MTA) cooperated with this work, providing details about each of their buses followed. In addition to MTA buses, other New York City passenger bus operators were also measured. In September 2000, MTA began to switch to 30 ppm sulfur diesel fuel while it is believed the non MTA operators did not. The measured emission ratios show that low sulfur fuel greatly reduces the amount of SO2 per CO2. Roughly one third of the MTA fleet of diesel buses have been equipped with the CRT retrofit. The gas phase results of interest in this category show increased direct emission of NO2 and companion work (also submitted to the 12th CRC) show the impact the CRT refit has on particulate emissions. CNG buses show increased H2CO and CH4 emission ratios relative to diesel powered motors.

State and Trends of the Global Carbon Budget

NASA Astrophysics Data System (ADS)

Canadell, J.

2017-12-01

Long-term redistribution of carbon among fossil fuel reserves, the atmosphere, oceans and land largely determines the degree of the human perturbation of the atmosphere and the climate system. Here I'll show a number of diagnostics to characterize changes in the global carbon cycle, including: 1) the continued growth in atmospheric CO2 despite an apparent stabilization in the growth of fossil fuel emissions and the likely emissions decline from land use change; 2) the growth in the land and ocean sinks in response to the rise in excess atmospheric CO2 with large annual and decadal variability; and 3) key drivers of these trends including the global greening, spatial distribution of carbons sinks, and responses to inter-annual variability. Efforts to attribute driving processes to the growing sinks require a strong CO2 fertilization effect on vegetation growth and emerging trends show an under realized role of semiarid regions in contributing to the mean, trend and variability of the global land sink. Climate variability, including ENSO and the 2000's slowdown in terrestrial global warming, has produced opportunities to explore the drivers of global carbon fluxes as they take large departures from mean states (e.g., high rates of atmospheric CO2 accumulation along with no growth in fossil fuel emissions and strong land greening trends in recent years). Process attribution shows the strong interplay between gross primary productivity and heterotrophic respiration in response to warming, and the role of tropical and sub-tropical systems to the overall sink. New advances in observations and data handling are critical in reducing uncertainties including 1) Bayesian fusion approaches to optimally combine multiple data streams of ocean and land uptake, and fossil fuel and land use change emissions; 2) continuous landscape carbon density measurements and column CO2 from remotely sensed platforms; and 3) improved ocean circulation and CO2 uptake at the decadal scales; among others. This presentation builds upon the work done by a team of international scientists under the umbrella of the Global Carbon Project.

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

NASA Astrophysics Data System (ADS)

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

2014-12-01

Measurements of CO2, CO, NOx and selected Volatile Organic Compounds (VOCs) mole fractions were performed continuously during a 10-day period in the Guy Môquet tunnel in Thiais, a peri-urban area about 15 km south of the centre of Paris, between 28 September and 8 October 2012. This data set is used here to identify the characteristics of traffic-emitted CO2 by evaluating its ratios to co-emitted species for the first time in the Paris region. High coefficients of determination (r2 > 0.7) are observed between CO2 and certain compounds that are characteristic of the traffic source (CO, NOx, benzene, xylenes and acetylene). Weak correlations (r2 < 0.2) are found with species such as propane, n-butane and i-butane that are associated with fuel evaporation, an insignificant source for CO2. To better characterise the traffic signal we focus only on species that are well-correlated with CO2 and on rush-hour periods characterised by the highest traffic-related mole fractions. From those mole fractions we remove the nighttime-average weekday mole fraction obtained for each species that we infer to be the most appropriate background signal for our study. Then we calculate observed Δspecies / ΔCO2 ratios, which we compare with the ones provided by the 2010 bottom-up high-resolved regional emission inventory from Airparif (the association in charge of monitoring the air quality in Île-de-France), focusing on local emission data for the specific road of the tunnel. We find an excellent agreement (2%) between the local inventory emission CO / CO2 ratio and our observed ΔCO / ΔCO2 ratio. Former tunnel experiments carried out elsewhere in the world provided observed ΔCO / ΔCO2 ratios that differ from 49 to 592% to ours. This variability can be related to technological improvement of vehicles, differences in driving conditions, and fleet composition. We also find a satisfactory agreement with the Airparif inventory for n-propylbenzene, n-pentane and xylenes to CO2 ratios. For most of the other species, the ratios obtained from the local emission inventory overestimate the observed ratios to CO2 by 34 to more than 300%. However, the emission ratios of NOx, o-xylene and i-pentane are underestimated by 30 to 79%. One main cause of such high differences between the inventory and our observations is likely the obsolete feature of the VOCs speciation matrix of the inventory that has not been updated since 1998, although law regulations on some VOCs have occurred since that time. Our study bears important consequences, discussed in the conclusion, for the characterisation of the urban CO2 plume and for atmospheric inverse modelling of urban CO2 emissions.

Greenhouse Gas Emissions Increase Following the Termination of a Perennial Legume Phase of an Annual Crop Rotation within the Red River Valley, Manitoba

NASA Astrophysics Data System (ADS)

Hanis, K. L.; Tenuta, M.; Amiro, B. D.; Glenn, A. J.; Maas, S.; Gervais, M.

2013-12-01

Perennial legume forages may have the potential to increase soil carbon sequestration and decrease nitrous oxide (N2O) emissions to the atmosphere when introduced into annual cropping systems. However, little is known about what short-term effect the return to annual cropping following termination of perennial legume forage would have on carbon dioxide (CO2) and N2O emissions. Furthermore, there are few quantitative measurements about this impact on the Canadian Prairies. A long-term field experiment to continuously measure CO2 and N2O fluxes was established at the Trace Gas Manitoba (TGAS-MAN) Long Term Greenhouse Gas Monitoring Site at Glenlea, Manitoba using the flux gradient micrometeorlogical technique with a tunable diode laser analyzer. The soil is poorly drained clay in the Red River Valley. The field experiment consisted of four 4-hectare plots planted to corn in 2006 and faba bean in 2007. In 2008, grass-alfalfa forage was introduced to two plots (annual - perennial) and grown until 2011 whereas the other two plots (annual) were planted to annual crops: spring wheat, rapeseed, barley and spring wheat in 2008, 2009, 2010 and 2011, respectively. In late September of 2011 the grass-alfalfa forage was killed and in 2012 all four plots were planted with corn. Termination of the grass-alfalfa forage resulted in greater fall CO2 emissions in 2011, greater spring melt CO2 emissions and net annual N2O emissions in 2012 from the annual-perennial plots when compared to the annual plots. Over seven crop years (2006-2012), the annual - perennial system increased carbon uptake by 3.4 Mg C ha-1 and reduced N2O emissions by 3.0 Mg CO2-eq ha-1 compared to the annual system. However after accounting for harvest removals both the annual and annual-perennial systems were net carbon sources of 5.7 and 2.5 Mg C ha-1 and net GHG sources of 38 and 24 Mg CO2-eq ha-1 respectively. We are currently following the long-term impacts of inclusion of perennial forages in an annual cropping system.

Sensitivity of Terrestrial Water and Energy Budgets to CO2-Physiological Forcing: An Investigation Using an Offline Land Model

NASA Technical Reports Server (NTRS)

Gopalakrishnan, Ranjith; Bala, Govindsamy; Jayaraman, Mathangi; Cao, Long; Nemani, Ramakrishna; Ravindranath, N. H.

2011-01-01

Increasing concentrations of atmospheric carbon dioxide (CO2) influence climate by suppressing canopy transpiration in addition to its well-known greenhouse gas effect. The decrease in plant transpiration is due to changes in plant physiology (reduced opening of plant stomata). Here, we quantify such changes in water flux for various levels of CO2 concentrations using the National Center for Atmospheric Research s (NCAR) Community Land Model. We find that photosynthesis saturates after 800 ppmv (parts per million, by volume) in this model. However, unlike photosynthesis, canopy transpiration continues to decline at about 5.1% per 100 ppmv increase in CO2 levels. We also find that the associated reduction in latent heat flux is primarily compensated by increased sensible heat flux. The continued decline in canopy transpiration and subsequent increase in sensible heat flux at elevated CO2 levels implies that incremental warming associated with the physiological effect of CO2 will not abate at higher CO2 concentrations, indicating important consequences for the global water and carbon cycles from anthropogenic CO2 emissions. Keywords: CO2-physiological effect, CO2-fertilization, canopy transpiration, water cycle, runoff, climate change 1.

Framing Climate Goals in Terms of Cumulative CO2-Forcing-Equivalent Emissions

NASA Astrophysics Data System (ADS)

Jenkins, S.; Millar, R. J.; Leach, N.; Allen, M. R.

2018-03-01

The relationship between cumulative CO2 emissions and CO2-induced warming is determined by the Transient Climate Response to Emissions (TCRE), but total anthropogenic warming also depends on non-CO2 forcing, complicating the interpretation of emissions budgets based on CO2 alone. An alternative is to frame emissions budgets in terms of CO2-forcing-equivalent (CO2-fe) emissions—the CO2 emissions that would yield a given total anthropogenic radiative forcing pathway. Unlike conventional "CO2-equivalent" emissions, these are directly related to warming by the TCRE and need to fall to zero to stabilize warming: hence, CO2-fe emissions generalize the concept of a cumulative carbon budget to multigas scenarios. Cumulative CO2-fe emissions from 1870 to 2015 inclusive are found to be 2,900 ± 600 GtCO2-fe, increasing at a rate of 67 ± 9.5 GtCO2-fe/yr. A TCRE range of 0.8-2.5°C per 1,000 GtC implies a total budget for 0.6°C of additional warming above the present decade of 880-2,750 GtCO2-fe, with 1,290 GtCO2-fe implied by the Coupled Model Intercomparison Project Phase 5 median response, corresponding to 19 years' CO2-fe emissions at the current rate.

Comparison of CO2 Emissions Data for 30 Cities from Different Sources

NASA Astrophysics Data System (ADS)

Nakagawa, Y.; Koide, D.; Ito, A.; Saito, M.; Hirata, R.

2017-12-01

Many sources suggest that cities account for a large proportion of global anthropogenic greenhouse gas emissions. Therefore, in search for the best ways to reduce total anthropogenic greenhouse gas emissions, a focus on the city emission is crucial. In this study, we collected CO2 emissions data in 30 cities during 1990-2015 and evaluated the degree of variance between data sources. The CO2 emissions data were obtained from academic papers, municipal reports, and high-resolution emissions maps (CIDIACv2016, EDGARv4.2, ODIACv2016, and FFDASv2.0). To extract urban CO2 emissions from the high-resolution emissions maps, urban fraction ranging from 0 to 1 was calculated for each 1×1 degree grid cell using the global land cover data (SYNMAP). Total CO2 emissions from the grid cells in which urban fraction occupies greater than or equal to 0.9 were regarded as urban CO2 emissions. The estimated CO2 emissions varied greatly depending on the information sources, even in the same year. There was a large difference between CO2 emissions collected from academic papers, municipal reports, and those extracted from high-resolution emissions maps. One reason is that they use different city boundaries. That is, the city proper (i.e. the political city boundary) is often defined as the city boundary in academic papers and municipal reports, whereas the urban area is used in the high-resolution emissions maps. Furthermore, there was a large variation in CO2 emissions collected from academic papers and municipal reports. These differences may be due to the difference in the assumptions such as allocation ratio of CO2 emissions to producers and consumers. In general, the consumption-based assignment of emissions gives higher estimates of urban CO2 emission in comparison with production-based assignment. Furthermore, there was also a large variation in CO2 emissions extracted from high-resolution emissions maps. This difference would be attributable to differences in information used in the spatial disaggregation of emissions. To identify the CO2 emissions from cities, it is necessary to determine common definitions of city boundaries, allocation ratio of CO2 emissions to consumption and production, and refined approach of the spatial disaggregation of CO2 emissions in high-resolution emissions maps.

The Anatomy of the Young Protostellar Outflow HH 211: Strong Evidence for CO v = 1-0 Fundamental Band Emission from Dense Gas in the Terminal Shock

NASA Astrophysics Data System (ADS)

Tappe, Achim; Forbrich, J.; Martín, S.; Lada, C. J.

2011-05-01

We present Spitzer Space Telescope 5-37 µm spectroscopic mapping observations toward the southeastern lobe of the young protostellar outflow HH 211 (part of IC 348 in Perseus, 260 pc). The terminal shock of the outflow shows a rich atomic and molecular spectrum with emission lines from OH, H2O, HCO+, CO2, H2, HD, [Fe II], [Si II], [Ne II], [S I], and [Cl I]. The spectrum also shows a rising continuum towards 5 µm, which we interpret as unresolved emission lines from highly excited rotational levels of the CO v=1-0 fundamental band. This interpretation is confirmed by a strong excess flux observed in the Spitzer IRAC 4-5 µm channel 2 image. We also observed the terminal outflow shock of this lobe with the Submillimeter Array (SMA) and detected pure rotational emission from CO 2-1, HCO+ 3-2, and HCN 3-2. The rotationally excited CO traces the collimated outflow and the terminal shock, whereas the vibrationally excited CO seen with Spitzer follows the continuation of the collimated outflow backbone in the terminal shock. The extremely high critical densities of the CO v=1-0 rovibrational lines indicate terminal shock jet densities larger than 107 cm-3. The unique combination of mid-infrared, submillimeter, and previous near-infrared observations allow us to gain detailed insights into the interaction of one of the youngest known protostellar outflows with its surrounding molecular cloud. Our results help to understand the nature of some of the so-called `green fuzzies’ (Extended Green Objects) identified by their Spitzer IRAC channel 2 excess and association with star-forming regions. They also provide a critical observational test to models of pulsed protostellar jets.

Geochemical monitoring of Taal volcano (Philippines) by means of diffuse CO2 degassing studies

NASA Astrophysics Data System (ADS)

Padrón, Eleazar; Hernández, Pedro A.; Arcilla, Carlo; Pérez, Nemesio M.; Lagmay, Alfredo M.; Rodríguez, Fátima; Quina, Gerald; Alonso, Mar; Padilla, Germán D.; Aurelio, Mario A.

2017-04-01

Observing changes in the discharge rate of CO2 is an important part of volcanic monitoring programs, because it is released by progressive depressurization of magma during ascent and reach the surface well before their parental magma. Taal Volcano in Southwest Luzon, Philippines, lies between a volcanic arc front facing the subduction zone along the Manila Trench and a volcanic field formed from extension beyond the arc front. Taal Volcano Island is formed by a main tuff cone surrounded by several smaller tuff cones, tuff rings and scoria cones. This island is located in the center of the 30 km wide Taal Caldera, now filled by Taal Lake. To monitor the volcanic activity of Taal volcano is a priority task in the Philippines, because several million people live within a 20-km radius of Taal's caldera rim. During the last period of volcanic unrest from 2010 to 2011, the main crater lake of Taal volcano released the highest diffuse CO2 emission rates through the water surface reported to date by volcanic lakes worldwide. The maximum CO2 emission rate measured in the study period occurred two months before the strongest seismic activity recorded during the unrest period (Arpa et al., 2013, Bull Volcanol 75:747). After the unrest period, diffuse CO2 emission has remained in the range 532-860 t/d in the period 2013-2016. In January 2016, an automatic geochemical station to monitor in a continuous mode the diffuse CO2 degassing in a selected location of Taal, was installed in January 2016 to improve the early warning system at the volcano. The station is located at Daang Kastila, at the northern portion of the main crater rim. It measures hourly the diffuse CO2 efflux, atmospheric CO2 concentration, soil water content and temperature, wind speed and direction, air temperature and humidity, rainfall, and barometric pressure. The 2016 time series show CO2 efflux values in the range 20-690 g m-2 d-1.Soil temperature, heavily influenced by rainfall, ranged between 74 and 96oC. Although short-temp fluctuations in the diffuse CO2 emission time series at Daang Kastila were partially driven by meteorological parameters, the main CO2 efflux changes were not driven by fluctuations of meteorological variables such as wind speed or barometric pressure and seem clearly to be associated with fluid pressure fluctuations in the volcanic system. These results showed the potential of applying continuous and discrete monitoring of soil CO2 efflux to improve and optimize the detection of early warning signals of future volcanic unrest at Taal volcano.

Emissions of mercury in southern Africa derived from long-term observations at Cape Point, South Africa

NASA Astrophysics Data System (ADS)

Brunke, E.-G.; Ebinghaus, R.; Kock, H. H.; Labuschagne, C.; Slemr, F.

2012-08-01

Mercury emissions in South Africa have so far been estimated only by a bottom-up approach from activities and emission factors for different processes. In this paper we derive GEM/CO (GEM being gaseous elemental mercury, Hg0), GEM/CO2, GEM/CH4, CO/CO2, CH4/CO2, and CH4/CO emission ratios from plumes observed during long-term monitoring of these species at Cape Point between March 2007 and December 2009. The average observed GEM/CO, GEM/CO2, GEM/CH4, CO/CO2, CH4/CO2, and CH4/CO emission ratios were 2.40 ± 2.65 pg m-3 ppb-1 (n = 47), 62.7 ± 80.2 pg m-3 ppm-1 (n = 44), 3.61 ± 4.66 pg m-3 ppb-1 (n = 46), 35.6 ± 25.4 ppb ppm-1 (n = 52), 20.2 ± 15.5 ppb ppm-1 (n = 48), and 0.876 ± 1.106 ppb ppb-1 (n = 42), respectively. The observed CO/CO2, CH4/CO2, and CH4/CO emission ratios agree within the combined uncertainties of the observations and emissions with the ratios calculated from EDGAR (version 4.2) CO2, CO, and CH4 inventories for South Africa and southern Africa (South Africa, Lesotho, Swaziland, Namibia, Botswana, Zimbabwe, and Mozambique) in 2007 and 2008 (inventories for 2009 are not available yet). Total elemental mercury emission of 13.1, 15.2, and 16.1 t Hg yr-1 are estimated independently using the GEM/CO, GEM/CO2, and GEM/CH4 emission ratios and the annual mean CO, CO2, and CH4 emissions, respectively, of South Africa in 2007 and 2008. The average of these independent estimates of 14.8 t GEM yr-1 is much less than the total emission of 257 t Hg yr-1 shown by older inventories which are now considered to be wrong. Considering the uncertainties of our emission estimate, of the emission inventories, and the fact that emission of GEM represents 50-78 % of all mercury emissions, our estimate is comparable to the currently cited GEM emissions in 2004 and somewhat smaller than emissions in 2006. A further increase of mercury emissions due to increasing electricity consumption will lead to a more pronounced difference. A quantitative assessment of the difference and its significance, however, will require emission inventories for the years of observations (2007-2009) as well as better data on the speciation of the total mercury emissions in South Africa.

Last chance for carbon capture and storage

NASA Astrophysics Data System (ADS)

Scott, Vivian; Gilfillan, Stuart; Markusson, Nils; Chalmers, Hannah; Haszeldine, R. Stuart

2013-02-01

Anthropogenic energy-related CO2 emissions are higher than ever. With new fossil-fuel power plants, growing energy-intensive industries and new sources of fossil fuels in development, further emissions increase seems inevitable. The rapid application of carbon capture and storage is a much heralded means to tackle emissions from both existing and future sources. However, despite extensive and successful research and development, progress in deploying carbon capture and storage has stalled. No fossil-fuel power plants, the greatest source of CO2 emissions, are using carbon capture and storage, and publicly supported demonstration programmes are struggling to deliver actual projects. Yet, carbon capture and storage remains a core component of national and global emissions-reduction scenarios. Governments have to either increase commitment to carbon capture and storage through much more active market support and emissions regulation, or accept its failure and recognize that continued expansion of power generation from burning fossil fuels is a severe threat to attaining objectives in mitigating climate change.

Development and Deployment of Mobile Emissions Laboratory for Continuous Long-Term Unattended Measurements of Greenhouse Gases, Fluxes, Isotopes and Pollutants

NASA Astrophysics Data System (ADS)

Gardner, A.; Baer, D. S.; Owano, T. G.; Provencal, R. A.; Gupta, M.; Parsotam, V.; Graves, P.; Goldstein, A.; Guha, A.

2010-12-01

Development and Deployment of Mobile Emissions Laboratory for Continuous Long-Term Unattended Measurements of Greenhouse Gases, Fluxes, Isotopes and Pollutants A. Gardner(1), D. Baer (1), T. Owano (1), R. Provencal (1), V. Parsotam (1), P. Graves (1), M. Gupta (1), Allen Goldstein (2), Abhinav Guha (2) (1) Los Gatos Research, 67 East Evelyn Avenue, Suite 3, Mountain View, CA 94041-1529 (2) Department of Environmental Science, Policy, and Management, University of California at Berkeley Quantifying the Urban Fossil Fuel Plume: Convergence of top-down and bottom-up approaches (Session A54). We report on the design, development and deployment of a novel Mobile Emissions Laboratory, consisting of innovative laser-based gas analyzers, for rapid measurements of multiple greenhouse gases and pollutants. Designed for real-time mobile and stationery emissions monitoring, the Mobile Emissions Laboratory was deployed at several locations during 2010, including CalNEX 2010, Caldecott Tunnel (Oakland, CA), and Altamont Landfill (Livermore, CA), to record real-time continuous measurements of isotopic CO2 (δ13C, CO2), methane (CH4), acetylene (C2H2), nitrous oxide (N2O), carbon monoxide (CO), and isotopic water vapor (H2O; δ18O, δ2H). The commercial gas analyzers are based on novel cavity-enhanced laser absorption spectroscopy. The portable analyzers provide measurements in real time, require about 150 watts (each) of power and do not need liquid nitrogen to operate. These instruments have been applied in the field for applications that require high data rates (for eddy correlation flux), wide dynamic range (e.g., for chamber flux and other applications with concentrations that can be 10-1000 times higher than typical ambient levels) and highest accuracy (atmospheric monitoring stations). The Mobile Emissions Laboratory, which contains onboard batteries for long-term unattended measurements without access to mains power, can provide regulatory agencies, monitoring stations, scientists and researchers with temporally and spatially resolved data (including measurements of important greenhouse gases, isotopes and pollutants) necessary for compliance monitoring, hot-spot detection, as well as cap and trade, at any location. Details of extended measurement campaigns (including lessons learned) at the various field sites (urban and rural environments) will be presented.

Analysis of non-regulated vehicular emissions by extractive FTIR spectrometry: tests on a hybrid car in Mexico City

NASA Astrophysics Data System (ADS)

Reyes, F.; Grutter, M.; Jazcilevich, A.; González-Oropeza, R.

2006-07-01

A methodology to acquire valuable information on the chemical composition and evolution of vehicular emissions is presented. The analysis of the gases is performed by passing a constant flow of a sample gas from the tail-pipe into a 10 L multi-pass cell. The absorption spectra within the cell are obtained using an FTIR spectrometer at 0.5 cm-1 resolution along a 13.1 m optical path. Additionally, the total flow from the exhaust is continuously measured from a differential pressure sensor on a Pitot tube installed at the exit of the exhaust. This configuration aims to obtain a good speciation capability by coadding spectra during 30 s and reporting the emission (in g/km) of key and non-regulated pollutants, such as CO2, CO, NO, SO2, NH3, HCHO, NMHC, during predetermined driving routines. The advantages and disadvantages of increasing the acquisition frequency, as well as the effect of other parameters such as spectral resolution, cell volume and flow rate, are discussed. With the aim of testing and evaluating the proposed technique, experiments were performed on a dynamometer running FTP-75 and typical driving cycles of the Mexico City Metropolitan Area (MCMA) on a Toyota Prius hybrid vehicle. This car is an example of recent automotive technology to reach the market dedicated to reduce emissions and therefore pressing the need of low detection techniques. This study shows the potential of the proposed technique to measure and report in real time the emissions of a large variety of pollutants, even from a super ultra-low emission vehicle (SULEV). The emissions of HC's, NOx, CO and CO2 obtained here are similar to experiments performed in other locations with the same vehicle model. Some differences suggest that an inefficient combustion process and type of gasoline used in the MCMA may be partly responsible for lower CO2 and higher CO and NO emission factors. Also, a fast reduction of NO emission to very low values is observed after cold ignition, giving rise to moderate N2O and eventually NH3 emissions. The proposed technique provides a tool for future studies comparing in detail the emissions of different technologies using alternative fuels and emission control systems.

The Net Climate Impact of Coal-Fired Power Plant Emissions

NASA Technical Reports Server (NTRS)

Shindell, D.; Faluvegi, G.

2010-01-01

Coal-fired power plants influence climate via both the emission of long-lived carbon dioxide (CO2) and short-lived ozone and aerosol precursors. Using a climate model, we perform the first study of the spatial and temporal pattern of radiative forcing specifically for coal plant emissions. Without substantial pollution controls, we find that near-term net global mean climate forcing is negative due to the well-known aerosol masking of the effects of CO2. Imposition of pollution controls on sulfur dioxide and nitrogen oxides leads to a rapid realization of the full positive forcing from CO2, however. Long-term global mean forcing from stable (constant) emissions is positive regardless of pollution controls. Emissions from coal-fired power plants until 1970, including roughly 1/3 of total anthropogenic CO2 emissions, likely contributed little net global mean climate forcing during that period though they may have induce weak Northern Hemisphere mid-latitude (NHml) cooling. After that time many areas imposed pollution controls or switched to low sulfur coal. Hence forcing due to emissions from 1970 to 2000 and CO2 emitted previously was strongly positive and contributed to rapid global and especially NHml warming. Most recently, new construction in China and India has increased rapidly with minimal application of pollution controls. Continuation of this trend would add negative near-term global mean climate forcing but severely degrade air quality. Conversely, following the Western and Japanese pattern of imposing air quality pollution controls at a later time could accelerate future warming rates, especially at NHmls. More broadly, our results indicate that due to spatial and temporal inhomogeneities in forcing, climate impacts of multi-pollutant emissions can vary strongly from region to region and can include substantial effects on maximum rate-of-change, neither of which are captured by commonly used global metrics. The method we introduce here to estimate regional temperature responses may provide additional insight.

The net climate impact of coal-fired power plant emissions

NASA Astrophysics Data System (ADS)

Shindell, D.; Faluvegi, G.

2010-04-01

Coal-fired power plants influence climate via both the emission of long-lived carbon dioxide (CO2) and short-lived ozone and aerosol precursors. Using a climate model, we perform the first study of the spatial and temporal pattern of radiative forcing specifically for coal plant emissions. Without substantial pollution controls, we find that near-term net global mean climate forcing is negative due to the well-known aerosol masking of the effects of CO2. Imposition of pollution controls on sulfur dioxide and nitrogen oxides leads to a rapid realization of the full positive forcing from CO2, however. Long-term global mean forcing from stable (constant) emissions is positive regardless of pollution controls. Emissions from coal-fired power plants until ~1970, including roughly 1/3 of total anthropogenic CO2 emissions, likely contributed little net global mean climate forcing during that period though they may have induce weak Northern Hemisphere mid-latitude (NHml) cooling. After that time many areas imposed pollution controls or switched to low-sulfur coal. Hence forcing due to emissions from 1970 to 2000 and CO2 emitted previously was strongly positive and contributed to rapid global and especially NHml warming. Most recently, new construction in China and India has increased rapidly with minimal application of pollution controls. Continuation of this trend would add negative near-term global mean climate forcing but severely degrade air quality. Conversely, following the Western and Japanese pattern of imposing air quality pollution controls at a later time could accelerate future warming rates, especially at NHmls. More broadly, our results indicate that due to spatial and temporal inhomogenaities in forcing, climate impacts of multi-pollutant emissions can vary strongly from region to region and can include substantial effects on maximum rate-of-change, neither of which are captured by commonly used global metrics. The method we introduce here to estimate regional temperature responses may provide additional insight.

Lifetime of carbon capture and storage as a climate-change mitigation technology

PubMed Central

Szulczewski, Michael L.; MacMinn, Christopher W.; Herzog, Howard J.; Juanes, Ruben

2012-01-01

In carbon capture and storage (CCS), CO2 is captured at power plants and then injected underground into reservoirs like deep saline aquifers for long-term storage. While CCS may be critical for the continued use of fossil fuels in a carbon-constrained world, the deployment of CCS has been hindered by uncertainty in geologic storage capacities and sustainable injection rates, which has contributed to the absence of concerted government policy. Here, we clarify the potential of CCS to mitigate emissions in the United States by developing a storage-capacity supply curve that, unlike current large-scale capacity estimates, is derived from the fluid mechanics of CO2 injection and trapping and incorporates injection-rate constraints. We show that storage supply is a dynamic quantity that grows with the duration of CCS, and we interpret the lifetime of CCS as the time for which the storage supply curve exceeds the storage demand curve from CO2 production. We show that in the United States, if CO2 production from power generation continues to rise at recent rates, then CCS can store enough CO2 to stabilize emissions at current levels for at least 100 y. This result suggests that the large-scale implementation of CCS is a geologically viable climate-change mitigation option in the United States over the next century. PMID:22431639

Emissions of mercury in Southern Africa derived from long-term observations at Cape Point, South Africa

NASA Astrophysics Data System (ADS)

Brunke, E.-G.; Ebinghaus, R.; Kock, H. H.; Labuschagne, C.; Slemr, F.

2012-05-01

Mercury emissions in South Africa have so far been estimated only by a bottom-up approach from activities and emission factors for different processes. In this paper we derive GEM/CO (GEM being gaseous elemental mercury, Hg0), GEM/CO2, GEM/CH4, CO/CO2, CH4/CO2, and CH4/CO emission ratios from plumes observed during long-term monitoring of these species at Cape Point between March 2007 and December 2009. The average observed GEM/CO, GEM/CO2, GEM/CH4, CO/CO2, CH4/CO2, and CH4/CO emission ratios were 2.40 ± 2.65 pg m-3 ppb-1 (n = 47), 62.7 ± 80.2 pg m-3 ppb-1 (n = 44), 3.61 ± 4.66 pg m-3 ppb-1 (n = 46), 35.6 ± 25.4 ppb ppm-1 (n = 52), 20.2 ± 15.5 ppb ppm-1 (n=48), and 0.876 ± 1.106 ppb ppm-1 (n=42), respectively. The observed CO/CO2, CH4/CO2, and CH4/CO emission ratios agree within the combined uncertainties of the observations and emissions with the ratios calculated from EDGAR (version 4.2) CO2, CO, and CH4 inventories for South Africa and Southern Africa (South Africa, Lesotho, Swaziland, Namibia, Botswana, Zimbabwe, and Mozambique) in 2007 and 2008 (inventories for 2009 are not available yet). Total elemental mercury emission of 13.1, 15.2, and 16.1 t Hg yr-1 are estimated independently using the GEM/CO, GEM/CO2, and GEM/CH4 emission ratios and the annual mean CO, CO2, and CH4 emissions, respectively, of South Africa in 2007 and 2008. The average of these independent estimates of 14.8 ± 1.5 t GEM yr-1 is much less than the total emission of 257 t Hg yr-1 from older inventories. Considering that emission of GEM represents only 50-78% of all mercury emissions, our estimates come close to the total mercury emission estimates ranging between 40-50 t Hg yr-1 from more recent inventories.

An evaluation of continuous emissions monitoring systems for improving industrial boiler efficiency

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

Eckerlin, H.M.; Hall, R.C.

1996-12-31

An experimental evaluation of currently available continuous emissions monitoring systems has been conducted at an industrial boiler facility. The analyzers used in the study represented a range of sensors and sampling systems. The performance of three systems was monitored and compared over a six-month period. Careful records were also kept on installation, calibration and maintenance requirements. Research results suggest that (at present) the close-coupled extractive systems using a zirconium oxide sensor (for O{sub 2}) and a catalytic combustibles sensor (for CO/combustibles) offer the most reliable, trouble-free performance. The project also provided valuable insights on a variety of issues relating tomore » the continuous monitoring of emissions from industrial boilers.« less

An evaluation of continuous emissions monitoring systems for improving industrial boiler efficiency

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

Eckerlin, H.M.; Hall, R.C.

1996-05-01

An experimental evaluation of currently available continuous emissions monitoring systems has been conducted at an industrial boiler facility. The analyzers used in the study represented a range of sensors and sampling systems. The performance of three systems was monitored and compared over a six-month period. Careful records were also kept on installation, calibration and maintenance requirements. Research results suggest that (at present) the close-coupled extractive systems using a zirconium oxide sensor (for O{sub 2}) and a catalytic combustibles sensor (for CO/combustibles) offer the most reliable, trouble-free performance. The project also provided valuable insights on a variety of issues relating tomore » the continuous monitoring of emissions from industrial boilers.« less

Young People's Burden: Requirement of Negative CO2 Emissions

NASA Technical Reports Server (NTRS)

Hansen, James; Sato, Makiko; Kharecha, Pushker; Von Schuckmann, Karina; Beerling, David J.; Cao, Junji; Marcott, Shaun; Masson-Delmotte, Valerie; Prather, Michael J.; Rohling, Eelco J.;

Young people's burden: requirement of negative CO2 emissions

NASA Astrophysics Data System (ADS)

Hansen, James; Sato, Makiko; Kharecha, Pushker; von Schuckmann, Karina; Beerling, David J.; Cao, Junji; Marcott, Shaun; Masson-Delmotte, Valerie; Prather, Michael J.; Rohling, Eelco J.; Shakun, Jeremy; Smith, Pete; Lacis, Andrew; Russell, Gary; Ruedy, Reto

2017-07-01

Global temperature is a fundamental climate metric highly correlated with sea level, which implies that keeping shorelines near their present location requires keeping global temperature within or close to its preindustrial Holocene range. However, global temperature excluding short-term variability now exceeds +1 °C relative to the 1880-1920 mean and annual 2016 global temperature was almost +1.3 °C. We show that global temperature has risen well out of the Holocene range and Earth is now as warm as it was during the prior (Eemian) interglacial period, when sea level reached 6-9 m higher than today. Further, Earth is out of energy balance with present atmospheric composition, implying that more warming is in the pipeline, and we show that the growth rate of greenhouse gas climate forcing has accelerated markedly in the past decade. The rapidity of ice sheet and sea level response to global temperature is difficult to predict, but is dependent on the magnitude of warming. Targets for limiting global warming thus, at minimum, should aim to avoid leaving global temperature at Eemian or higher levels for centuries. Such targets now require negative emissions, i.e., extraction of CO2 from the air. If phasedown of fossil fuel emissions begins soon, improved agricultural and forestry practices, including reforestation and steps to improve soil fertility and increase its carbon content, may provide much of the necessary CO2 extraction. In that case, the magnitude and duration of global temperature excursion above the natural range of the current interglacial (Holocene) could be limited and irreversible climate impacts could be minimized. In contrast, continued high fossil fuel emissions today place a burden on young people to undertake massive technological CO2 extraction if they are to limit climate change and its consequences. Proposed methods of extraction such as bioenergy with carbon capture and storage (BECCS) or air capture of CO2 have minimal estimated costs of USD 89-535 trillion this century and also have large risks and uncertain feasibility. Continued high fossil fuel emissions unarguably sentences young people to either a massive, implausible cleanup or growing deleterious climate impacts or both.

Tundra ecosystems observed to be CO2 sources due to differential amplification of the carbon cycle.

PubMed

Belshe, E F; Schuur, E A G; Bolker, B M

2013-10-01

Are tundra ecosystems currently a carbon source or sink? What is the future trajectory of tundra carbon fluxes in response to climate change? These questions are of global importance because of the vast quantities of organic carbon stored in permafrost soils. In this meta-analysis, we compile 40 years of CO2 flux observations from 54 studies spanning 32 sites across northern high latitudes. Using time-series analysis, we investigated if seasonal or annual CO2 fluxes have changed over time, and whether spatial differences in mean annual temperature could help explain temporal changes in CO2 flux. Growing season net CO2 uptake has definitely increased since the 1990s; the data also suggest (albeit less definitively) an increase in winter CO2 emissions, especially in the last decade. In spite of the uncertainty in the winter trend, we estimate that tundra sites were annual CO2 sources from the mid-1980s until the 2000s, and data from the last 7 years show that tundra continue to emit CO2 annually. CO2 emissions exceed CO2 uptake across the range of temperatures that occur in the tundra biome. Taken together, these data suggest that despite increases in growing season uptake, tundra ecosystems are currently CO2 sources on an annual basis. © 2013 John Wiley & Sons Ltd/CNRS.

Imaging volcanic CO2 and SO2

NASA Astrophysics Data System (ADS)

Gabrieli, A.; Wright, R.; Lucey, P. G.; Porter, J. N.

2017-12-01

Detecting and quantifying volcanic carbon dioxide (CO2) and sulfur dioxide (SO2) emissions is of relevance to volcanologists. Changes in the amount and composition of gases that volcanoes emit are related to subsurface magma movements and the probability of eruptions. Volcanic gases and related acidic aerosols are also an important atmospheric pollution source that create environmental health hazards for people, animals, plants, and infrastructures. For these reasons, it is important to measure emissions from volcanic plumes during both day and night. We present image measurements of the volcanic plume at Kīlauea volcano, HI, and flux derivation, using a newly developed 8-14 um hyperspectral imaging spectrometer, the Thermal Hyperspectral Imager (THI). THI is capable of acquiring images of the scene it views from which spectra can be derived from each pixel. Each spectrum contains 50 wavelength samples between 8 and 14 um where CO2 and SO2 volcanic gases have diagnostic absorption/emission features respectively at 8.6 and 14 um. Plume radiance measurements were carried out both during the day and the night by using both the lava lake in the Halema'uma'u crater as a hot source and the sky as a cold background to detect respectively the spectral signatures of volcanic CO2 and SO2 gases. CO2 and SO2 path-concentrations were then obtained from the spectral radiance measurements using a new Partial Least Squares Regression (PLSR)-based inversion algorithm, which was developed as part of this project. Volcanic emission fluxes were determined by combining the path measurements with wind observations, derived directly from the images. Several hours long time-series of volcanic emission fluxes will be presented and the SO2 conversion rates into aerosols will be discussed. The new imaging and inversion technique, discussed here, are novel allowing for continuous CO2 and SO2 plume mapping during both day and night.

Definition of yearly emission factor of dust and greenhouse gases through continuous measurements in swine husbandry

NASA Astrophysics Data System (ADS)

Costa, Annamaria; Guarino, Marcella

The object of this study was to develop an accurate estimation method to evaluate the contribution of the various compartments of swine husbandry to dust and GHG (greenhouse gases, CO 2, CH 4 and N 2O) emission into the atmosphere during one year of observation. A weaning, a gestation, a farrowing and a fattening room in an intensive pig house were observed in three different periods (Autumn-Winter, Springtime and Summer, monitoring at least 60% of each period (20% at the beginning, in the middle and at the end) of each cycle). During monitoring, live weight, average live weight gain, number of animals and its variation, type of feed and feeding time were taken into account to evaluate their influence on PM 10, or the fraction of suspended particulate matter with an aerodynamic diameter less than or equal to 10 μm [Emission Inventory Guidebook, 2007. B1100 Particle Emissions from Animal Husbandry Activities. Available from: (accessed October 2008)] and to define GHG emission. The selected piggery had a ventilation control system using a free running impeller to monitor continuously real-time environmental and management parameters with an accuracy of 5%. PM 10 concentration was monitored by a sampler (Haz Dust EPAM 5000), either continuously or through traditional gravimetric technique, and the mean value of dust amount collected on the membranes was utilized as a correction factor to be applied to continuously collected data. PM 10 concentration amount incoming from inlets was removed from PM 10 emission calculation, to estimate the real contribution of pig house dust pollution into atmosphere. Mean yearly emission factor of PM 10 was measured in 2 g d -1 LU -1 for the weaning room, 0.09 g d -1 LU -1 for the farrowing room, 2.59 g d -1 LU -1 for the fattening room and 1.23 g d -1 LU -1 for the gestation room. The highest PM 10 concentration and emission per LU was recorded in the fattening compartment while the lowest value was recorded in the farrowing room. CO 2, CH 4 and N 2O concentrations were continuously measured in the exhaust ducts using an infrared photoacoustic detector IPD (Brüel & Kjaer, Multi-gas Monitor Type 1302, Multipoint Sampler and Doser Type 1303) sampling data every 15 min, for the 60% of the cycles. Yearly emission factor for CO 2 was measured in 5997 g d -1 LU -1 for the weaning room, 1278 g d -1 LU -1 for the farrowing room, 13,636 g d -1 LU -1 for the fattening room and 8851 g d -1 LU -1 for the gestation room. Yearly emission factor for CH 4 was measured in 24.57 g d -1 LU -1 for the weaning room, 4.68 g d -1 LU -1 for the farrowing room, 189.82 g d -1 LU -1 for the fattening room and 132.12 g d -1 LU -1 for the gestation room. Yearly emission factor for N 2O was measured in 3.62 g d -1 LU -1 for the weaning room, 0.66 g d -1 LU -1 for the farrowing room, 3.26 g d -1 LU -1 for the fattening room and 2.72 g d -1 LU -1 for the gestation room.

Estimates of CO2 from fires in the United States: implications for carbon management.

PubMed

Wiedinmyer, Christine; Neff, Jason C

2007-11-01

Fires emit significant amounts of CO2 to the atmosphere. These emissions, however, are highly variable in both space and time. Additionally, CO2 emissions estimates from fires are very uncertain. The combination of high spatial and temporal variability and substantial uncertainty associated with fire CO2 emissions can be problematic to efforts to develop remote sensing, monitoring, and inverse modeling techniques to quantify carbon fluxes at the continental scale. Policy and carbon management decisions based on atmospheric sampling/modeling techniques must account for the impact of fire CO2 emissions; a task that may prove very difficult for the foreseeable future. This paper addresses the variability of CO2 emissions from fires across the US, how these emissions compare to anthropogenic emissions of CO2 and Net Primary Productivity, and the potential implications for monitoring programs and policy development. Average annual CO2 emissions from fires in the lower 48 (LOWER48) states from 2002-2006 are estimated to be 213 (+/- 50 std. dev.) Tg CO2 yr-1 and 80 (+/- 89 std. dev.) Tg CO2 yr-1 in Alaska. These estimates have significant interannual and spatial variability. Needleleaf forests in the Southeastern US and the Western US are the dominant source regions for US fire CO2 emissions. Very high emission years typically coincide with droughts, and climatic variability is a major driver of the high interannual and spatial variation in fire emissions. The amount of CO2 emitted from fires in the US is equivalent to 4-6% of anthropogenic emissions at the continental scale and, at the state-level, fire emissions of CO2 can, in some cases, exceed annual emissions of CO2 from fossil fuel usage. The CO2 released from fires, overall, is a small fraction of the estimated average annual Net Primary Productivity and, unlike fossil fuel CO2 emissions, the pulsed emissions of CO2 during fires are partially counterbalanced by uptake of CO2 by regrowing vegetation in the decades following fire. Changes in fire severity and frequency can, however, lead to net changes in atmospheric CO2 and the short-term impacts of fire emissions on monitoring, modeling, and carbon management policy are substantial.

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

NASA Technical Reports Server (NTRS)

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

2014-01-01

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

CarbonSat -Quantification of natural and man-made greenhouse gas surface fluxes from satellite observations of atmospheric CO2 and CH4 column amounts

NASA Astrophysics Data System (ADS)

Bovensmann, Heinrich; Buchwitz, M.; Burrows, J. P.; Notholt, J.; Bovensmann, H.; Reuter, M.; Trautmann, T.; Ehret, G.; Heimann, M.; Monks, P.; B&Ü, H.; Sch; Harding, R.; Quegan, S.; Rayner, P.; Breon, F. M.; Bergam-O Aschi, P.; Dittus, H. J.; Erzinger, J.; Crisp, D.

Surprisingly and in spite of their exceptional driving role in climate change, our knowledge about the variable sources and sinks of the greenhouse gases CO2 and CH4 is currently inadequate. For example, the ability of the Earth-atmosphere system to buffer increasing anthropogenic emissions into the atmosphere has large uncertainties and emissions from many sources (geo-logic, anthropogenic, biogenic) are to a large degree uncertain. An adequate knowledge of the sources and sinks of CO2 and CH4 and their response to a changing climate is a pre-requisite for the accurate prediction of the regional variation of the climate of our planet. CarbonSat is a new mission concept to quantify and monitor CO2 and CH4 sources and sinks at the regional to local scale. The data will allow a better understanding of the processes that control the Carbon Cycle dynamics and an independent estimate of local greenhouse gas emissions (fossil fuel, geological CO2 and CH4, etc.). This will be achieved by a unique combination of high spatial resolution passive and active compact remote sensing with inverse modeling techniques. CarbonSat will accurately measure column-averaged mixing ratios of CO2 and CH4, i.e., XCO2 and XCH4, at a spatial resolution of 2 x 2 km2 (500 km continuous swath) with 0.5 percent goal (1 percent threshold) single measurement precision and global coverage within 3-6 days. Beside the quantification of sources and sinks on the regional scale, one key and innovative aim of the CarbonSat mission is to go a step forward towards quantifying local emission hot spots (fossil fuel emissions by power plants, gas/oil production, geological sources etc.). The core sensor will be a compact Imaging NIR/SWIR spectrometer (SCIAMACHY, OCO her-itage) whose measurements yield global data sets of XCO2 and XCH4 with at least one order of magnitude higher number of cloud free measurements than GOSAT and OCO and one order of magnitude better spatial coverage than OCO, due to CarbonSat's 500 km swath continuous across track coverage with 2 x 2 km2 spatial resolution. Ideally, the imaging spectrometer will be accompanied by a compact CH4 Lidar, to derive complementary accurate XCH4 -especially in high northern latitudes -as well as information on clouds and vegetation height. The overall mission concept will be presented.

CarbonSat - Quantification of natural and man-made greenhouse gas surface fluxes from satellite observations of atmospheric CO2 and CH4 column amounts

NASA Astrophysics Data System (ADS)

Bovensmann, Heinrich; Buchwitz, Michael

2010-05-01

Surprisingly and in spite of their exceptional driving role in climate change, our knowledge about the variable sources and sinks of the greenhouse gases CO2 and CH4 is currently inadequate. For example, the ability of the Earth-atmosphere system to buffer increasing anthropogenic emissions into the atmosphere has large uncertainties and emissions from many sources (geologic, anthropogenic, biogenic) are to a large degree uncertain. An adequate knowledge of the sources and sinks of CO2 and CH4 and their response to a changing climate is a pre-requisite for the accurate prediction of the regional variation of the climate of our planet. CarbonSat is a new mission concept to quantify and monitor CO2 and CH4 sources and sinks at the regional to local scale. The data will allow a better understanding of the processes that control the Carbon Cycle dynamics and an independent estimate of local greenhouse gas emissions (fossil fuel, geological CO2 and CH4, etc.). This will be achieved by a unique combination of high spatial resolution passive and active compact remote sensing with inverse modeling techniques. CarbonSat will accurately measure column-averaged mixing ratios of CO2 and CH4, i.e., XCO2 and XCH4, at a spatial resolution of 2 x 2 km2 (500 km continuous swath) with 0.5% goal (1%, threshold) single measurement precision and global coverage within 3-6 days. Beside the quantification of sources and sinks on the regional scale, one key and innovative aim of the CarbonSat mission is to go a step forward towards quantifying local emission hot spots (fossil fuel emissions by power plants, gas/oil production, geological sources etc.). The core sensor will be a compact Imaging NIR/SWIR spectrometer (SCIAMACHY, OCO heritage) whose measurements yield global data sets of XCO2 and XCH4 with at least one order of magnitude higher number of cloud free measurements than GOSAT and OCO and one order of magnitude better spatial coverage than OCO, due to CarbonSat's 500 km swath continuous across track coverage with 2 x 2 km2 spatial resolution. Ideally, the imaging spectrometer will be accompanied by a compact CH4 Lidar, to derive complementary accurate XCH4 - especially in high northern latitudes - as well as information on clouds and vegetation height. The overall mission concept, the expected data quality and selected application areas will be presented.

Does replacing coal with wood lower CO2 emissions? Dynamic lifecycle analysis of wood bioenergy

NASA Astrophysics Data System (ADS)

Sterman, John D.; Siegel, Lori; Rooney-Varga, Juliette N.

2018-01-01

Bioenergy is booming as nations seek to cut their greenhouse gas emissions. The European Union declared biofuels to be carbon-neutral, triggering a surge in wood use. But do biofuels actually reduce emissions? A molecule of CO2 emitted today has the same impact on radiative forcing whether it comes from coal or biomass. Biofuels can only reduce atmospheric CO2 over time through post-harvest increases in net primary production (NPP). The climate impact of biofuels therefore depends on CO2 emissions from combustion of biofuels versus fossil fuels, the fate of the harvested land and dynamics of NPP. Here we develop a model for dynamic bioenergy lifecycle analysis. The model tracks carbon stocks and fluxes among the atmosphere, biomass, and soils, is extensible to multiple land types and regions, and runs in ≈1s, enabling rapid, interactive policy design and sensitivity testing. We simulate substitution of wood for coal in power generation, estimating the parameters governing NPP and other fluxes using data for forests in the eastern US and using published estimates for supply chain emissions. Because combustion and processing efficiencies for wood are less than coal, the immediate impact of substituting wood for coal is an increase in atmospheric CO2 relative to coal. The payback time for this carbon debt ranges from 44-104 years after clearcut, depending on forest type—assuming the land remains forest. Surprisingly, replanting hardwood forests with fast-growing pine plantations raises the CO2 impact of wood because the equilibrium carbon density of plantations is lower than natural forests. Further, projected growth in wood harvest for bioenergy would increase atmospheric CO2 for at least a century because new carbon debt continuously exceeds NPP. Assuming biofuels are carbon neutral may worsen irreversible impacts of climate change before benefits accrue. Instead, explicit dynamic models should be used to assess the climate impacts of biofuels.

A small, lightweight multipollutant sensor system for ground-mobile and aerial emission sampling from open area sources

NASA Astrophysics Data System (ADS)

Zhou, Xiaochi; Aurell, Johanna; Mitchell, William; Tabor, Dennis; Gullett, Brian

2017-04-01

Characterizing highly dynamic, transient, and vertically lofted emissions from open area sources poses unique measurement challenges. This study developed and applied a multipollutant sensor and time-integrated sampler system for use on mobile applications such as vehicles, tethered balloons (aerostats) and unmanned aerial vehicles (UAVs) to determine emission factors. The system is particularly applicable to open area sources, such as forest fires, due to its light weight (3.5 kg), compact size (6.75 L), and internal power supply. The sensor system, termed ;Kolibri;, consists of sensors measuring CO2 and CO, and samplers for particulate matter (PM) and volatile organic compounds (VOCs). The Kolibri is controlled by a microcontroller which can record and transfer data in real time through a radio module. Selection of the sensors was based on laboratory testing for accuracy, response delay and recovery, cross-sensitivity, and precision. The Kolibri was compared against rack-mounted continuous emissions monitoring system (CEMs) and another mobile sampling instrument (the ;Flyer;) that has been used in over ten open area pollutant sampling events. Our results showed that the time series of CO, CO2, and PM2.5 concentrations measured by the Kolibri agreed well with those from the CEMs and the Flyer, with a laboratory-tested percentage error of 4.9%, 3%, and 5.8%, respectively. The VOC emission factors obtained using the Kolibri were consistent with existing literature values that relate concentration to modified combustion efficiency. The potential effect of rotor downwash on particle sampling was investigated in an indoor laboratory and the preliminary results suggested that its influence is minimal. Field application of the Kolibri sampling open detonation plumes indicated that the CO and CO2 sensors responded dynamically and their concentrations co-varied with emission transients. The Kolibri system can be applied to various challenging open area scenarios such as fires, lagoons, flares, and landfills.

Effects of three years of simulated nitrogen deposition on soil nitrogen dynamics and greenhouse gas emissions in a Korean pine plantation of northeast China.

PubMed

Song, Lei; Tian, Peng; Zhang, Jinbo; Jin, Guangze

2017-12-31

Continuously enhanced nitrogen (N) deposition alters the pattern of N and carbon (C) transformations, and thus influences greenhouse gas emissions. It is necessary to clarify the effect of N deposition on greenhouse gas emissions and soil N dynamics for an accurate assessment of C and N budgets under increasing N deposition. In this study, four simulated N deposition treatments (control [CK: no N addition], low-N [L: 20kgNha -1 yr -1 ], medium-N [M: 40kgNha -1 yr -1 ], and high-N [H: 80kgNha -1 yr -1 ]) were operated from 2014. Carbon dioxide, methane and nitrous oxide fluxes were monitored semimonthly, as were soil variables such as temperature, moisture and the concentrations of total dissolved N (TDN), NO 3 - , NO 2 - , NH 4 + , and dissolved organic N (DON) in soil solutions. The simulated N deposition resulted in a significant increase in TDN, NO 3 - and DON concentrations in soil solutions. The average CO 2 emission rate ranged from 222.6mgCO 2 m -2 h -1 in CK to 233.7mgCO 2 m -2 h -1 in the high-N treatment. Three years of simulated N deposition had no effect on soil CO 2 emission, which was mainly controlled by soil temperature. The mean N 2 O emission rate during the whole 3years was 0.02mgN 2 Om -2 h -1 for CK, which increased significantly to 0.05mgN 2 Om -2 h -1 in the high-N treatment. The N 2 O emission rate positively correlated with NH 4 + concentrations, and negatively correlated with soil moisture. The average CH 4 flux during the whole 3years was -0.74μgCH 4 m -2 h -1 in CK, which increased to 1.41μgCH 4 m -2 h -1 in the low-N treatment. CH 4 flux positively correlated with NO 3 - concentrations. These results indicate that short-term N deposition did not affect soil CO 2 emissions, while CH 4 and N 2 O emissions were sensitive to N deposition. Copyright © 2017 Elsevier B.V. All rights reserved.

40 CFR 63.6640 - How do I demonstrate continuous compliance with the emission limitations, operating limitations...

Code of Federal Regulations, 2014 CFR

2014-07-01

.... (4) If you are demonstrating compliance with the THC percent reduction requirement, you must measure THC emissions using Method 25A, reported as propane, of 40 CFR part 60, appendix A. (5) You must... determine O2 concentration must be made at the same time as the measurements for CO or THC concentration. (6...

40 CFR 63.6640 - How do I demonstrate continuous compliance with the emission limitations, operating limitations...

Code of Federal Regulations, 2013 CFR

2013-07-01

.... (4) If you are demonstrating compliance with the THC percent reduction requirement, you must measure THC emissions using Method 25A, reported as propane, of 40 CFR part 60, appendix A. (5) You must... determine O2 concentration must be made at the same time as the measurements for CO or THC concentration. (6...

First Continuous High Frequency in Situ Measurements of CO2 and CH4 in Rwanda Using Cavity Ring-Down Spectroscopy, and Preliminary Results of Regional Emission Estimation

NASA Astrophysics Data System (ADS)

Gasore, J.; Prinn, R. G.

2016-12-01

Recent IPCC reports emphasize the lack of ground measurements of greenhouse gases on the African continent, despite Africa's significant emissions from agriculture and biomass burning as well as ongoing land use changes. We have established a greenhouse gas monitoring station in northern Rwanda that will be part of the Advanced Global Atmospheric Gases Experiment (AGAGE), a global network of high frequency long-term remote atmospheric measurement stations. Using a Picarro G2401 cavity ring-down analyzer, continuous measurements of CO2, CH4, and CO at a frequency of five seconds are being captured at this equatorial East African site. The measurement site is located near the Virunga mountains, a volcanic range in North-West Rwanda, on the summit of Mt. Mugogo (2507 m above sea level). Mt. Mugogo is located in a rural area 70km away from Kigali, the capital of Rwanda, and about 13km from the nearest town. From HYSPLIT 7-day back-trajectory calculations, we have determined that the station measures air masses originating from East and Central Africa, the Indian Ocean and occasionally from Southern Asia. Here we present the first greenhouse gas measurement data from this understudied location in Africa. We also present preliminary results of regional CO2 and CH4emissions estimation from this unique dataset, using the Numerical Atmospheric-dispersion Modeling Environment (NAME) lagrangian particle dispersion model.

Monitoring gas and heat emissions at Norris Geyser Basin, Yellowstone National Park, USA based on a combined eddy covariance and Multi-GAS approach

NASA Astrophysics Data System (ADS)

Lewicki, J. L.; Kelly, P. J.; Bergfeld, D.; Vaughan, R. G.; Lowenstern, J. B.

2017-11-01

We quantified gas and heat emissions in an acid-sulfate, vapor-dominated area (0.04-km2) of Norris Geyser Basin, located just north of the 0.63 Ma Yellowstone Caldera and near an area of anomalous uplift. From 14 May to 3 October 2016, an eddy covariance system measured half-hourly CO2, H2O and sensible (H) and latent (LE) heat fluxes and a Multi-GAS instrument measured (1 Hz frequency) atmospheric H2O, CO2 and H2S volumetric mixing ratios. We also measured soil CO2 fluxes using the accumulation chamber method and temperature profiles on a grid and collected fumarole gas samples for geochemical analysis. Eddy covariance CO2 fluxes ranged from - 56 to 885 g m- 2 d- 1. Using wavelet analysis, average daily eddy covariance CO2 fluxes were locally correlated with average daily environmental parameters on several-day to monthly time scales. Estimates of CO2 emission rate from the study area ranged from 8.6 t d- 1 based on eddy covariance measurements to 9.8 t d- 1 based on accumulation chamber measurements. Eddy covariance water vapor fluxes ranged from 1178 to 24,600 g m- 2 d- 1. Nighttime H and LE were considered representative of hydrothermal heat fluxes and ranged from 4 to 183 and 38 to 504 W m- 2, respectively. The total hydrothermal heat emission rate (H + LE + radiant) estimated for the study area was 11.6 MW and LE contributed 69% of the output. The mean ± standard deviation of H2O, CO2 and H2S mixing ratios measured by the Multi-GAS system were 9.3 ± 3.1 parts per thousand, 467 ± 61 ppmv, and 0.5 ± 0.6 ppmv, respectively, and variations in the gas compositions were strongly correlated with diurnal variations in environmental parameters (wind speed and direction, atmospheric temperature). After removing ambient H2O and CO2, the observed variations in the Multi-GAS data could be explained by the mixing of relatively H2O-CO2-H2S-rich fumarole gases with CO2-rich and H2O-H2S-poor soil gases. The fumarole H2O/CO2 and CO2/H2S end member ratios (101.7 and 27.1, respectively, on average) were invariant during the measurement period and fell within the range of values measured in direct fumarole gas samples. The soil gas H2O/CO2 end member ratios ( 15-30) were variable and low relative to the fumarole end member, likely resulting from water vapor loss during cooling and condensation in the shallow subsurface, whereas the CO2/H2S end member ratio was high ( 160), presumably related to transport of CO2-dominated soil gas emissions mixed with trace fumarolic emissions to the Multi-GAS station. Nighttime eddy covariance ratios of H2O to CO2 flux were typically between the soil gas and fumarole end member H2O/CO2 ratios defined by Multi-GAS measurements. Overall, the combined eddy covariance and Multi-GAS approach provides a powerful tool for quasi-continuous measurements of gas and heat emissions for improved volcano-hydrothermal monitoring.

Global Warming in the 21st Century: An Alternate Scenario

NASA Technical Reports Server (NTRS)

Hansen, James E.; Sato, Makiko; Ruedy, Reto; Lacis, Andrew; Oinas, Valdar

2000-01-01

A common view is that the current global warming rate will continue or accelerate. But we argue that rapid warming in recent decades has been driven by non-CO2 greenhouse gases (GHGs), such as CFCs, CH4 and N2O, not by the products of fossil fuel burning, CO2 and aerosols, whose positive and negative climate forcings are partially offsetting. The growth rate of non-CO2 GHGs has declined in the past decade. If sources of CH4 and O3 precursors were reduced in the future, the change of climate forcing by non-CO2 GHGs In the next 50 years could be near zero. Combined with a reduction of black carbon emissions and plausible success in slowing CO2 emissions, this could lead to a decline in the rate of global warming, reducing the danger of dramatic climate change. Such a focus on air pollution has practical benefits that unite the interests of developed and developing countries. However, assessment of ongoing and future climate change requires composition-specific longterm global monitoring of aerosol properties.

Reversible and irreversible impacts of greenhouse gas emissions in multi-century projections with the NCAR global coupled carbon cycle-climate model

NASA Astrophysics Data System (ADS)

Froelicher, T. L.; Joos, F.

2010-12-01

The legacy of historical and the long-term impacts of 21st century greenhouse gas emissions on climate, ocean acidification, and carbon-climate feedbacks are investigated with a coupled carbon cycle-climate model. Emission commitment scenarios with zero emissions after year 2100 and 21st century emissions of 1,800, 900, and 0 gigatons of carbon are run up to year 2500. The reversibility and irreversibility of impacts is quantified by comparing anthropogenically-forced regional changes with internal, unforced climate variability. We show that the influence of historical emissions and of non-CO2 agents is largely reversible on the regional scale. Forced changes in surface temperature and precipitation become smaller than internal variability for most land and ocean grid cells in the absence of future carbon emissions. In contrast, continued carbon emissions over the 21st century cause irreversible climate change on centennial to millennial timescales in most regions and impacts related to ocean acidification and sea level rise continue to aggravate for centuries even if emissions are stopped in year 2100. Undersaturation of the Arctic surface ocean with respect to aragonite, a mineral form of calcium carbonate secreted by marine organisms, is imminent and remains widespread. The volume of supersaturated water providing habitat to calcifying organisms is reduced from preindustrial 40 to 25% in 2100 and to 10% in 2300 for the high emission case. We conclude that emission trading schemes, related to the Kyoto Process,should not permit trading between emissions of relatively short-lived agents and CO2 given the irreversible impacts of anthropogenic carbon emissions.

Reversible and irreversible impacts of greenhouse gas emissions in multi-century projections with the NCAR global coupled carbon cycle-climate model

NASA Astrophysics Data System (ADS)

Frölicher, Thomas L.; Joos, Fortunat

2010-12-01

The legacy of historical and the long-term impacts of 21st century greenhouse gas emissions on climate, ocean acidification, and carbon-climate feedbacks are investigated with a coupled carbon cycle-climate model. Emission commitment scenarios with zero emissions after year 2100 and 21st century emissions of 1,800, 900, and 0 gigatons of carbon are run up to year 2500. The reversibility and irreversibility of impacts is quantified by comparing anthropogenically-forced regional changes with internal, unforced climate variability. We show that the influence of historical emissions and of non-CO2 agents is largely reversible on the regional scale. Forced changes in surface temperature and precipitation become smaller than internal variability for most land and ocean grid cells in the absence of future carbon emissions. In contrast, continued carbon emissions over the 21st century cause irreversible climate change on centennial to millennial timescales in most regions and impacts related to ocean acidification and sea level rise continue to aggravate for centuries even if emissions are stopped in year 2100. Undersaturation of the Arctic surface ocean with respect to aragonite, a mineral form of calcium carbonate secreted by marine organisms, is imminent and remains widespread. The volume of supersaturated water providing habitat to calcifying organisms is reduced from preindustrial 40 to 25% in 2100 and to 10% in 2300 for the high emission case. We conclude that emission trading schemes, related to the Kyoto Process, should not permit trading between emissions of relatively short-lived agents and CO2 given the irreversible impacts of anthropogenic carbon emissions.

State of energy consumption and CO2 emission in Bangladesh.

PubMed

Azad, Abul K; Nashreen, S W; Sultana, J

2006-03-01

Carbon dioxide (CO2) is one of the most important gases in the atmosphere, and is necessary for sustaining life on Earth. It is also considered to be a major greenhouse gas contributing to global warming and climate change. In this article, energy consumption in Bangladesh is analyzed and estimates are made of CO2 emission from combustion of fossil fuel (coal, gas, petroleum products) for the period 1977 to 1995. International Panel for Climate Change guidelines for national greenhouse gas inventories were used in estimating CO2 emission. An analysis of energy data shows that the consumption of fossil fuels in Bangladesh is growing by more than 5% per year. The proportion of natural gas in total energy consumption is increasing, while that of petroleum products and coal is decreasing. The estimated total CO2 release from all primary fossil fuels used in Bangladesh amounted to 5072 Gigagram (Gg) in 1977, and 14 423 Gg in 1995. The total amounts of CO2 released from petroleum products, natural gas, and coal in the period 1977-1995 were 83 026 Gg (50% of CO2 emission), 72 541 Gg (44% of CO2 emission), and 9545 Gg (6% CO2 emission), respectively. A trend in CO2 emission with projections to 2070 is generated. In 2070, total estimated CO2 emission will be 293 260 Gg with a current growth rate of 6.34% y . CO2 emission from fossil fuels is increasing. Petroleum products contribute the majority of CO2 emission load, and although the use of natural gas is increasing rapidly, its contribution to CO2 emission is less than that of petroleum products. The use of coal as well as CO2 emission from coal is expected to gradually decrease.

Global and regional drivers of accelerating CO2 emissions

PubMed Central

Raupach, Michael R.; Marland, Gregg; Ciais, Philippe; Le Quéré, Corinne; Canadell, Josep G.; Klepper, Gernot; Field, Christopher B.

2007-01-01

CO2 emissions from fossil-fuel burning and industrial processes have been accelerating at a global scale, with their growth rate increasing from 1.1% y−1 for 1990–1999 to >3% y−1 for 2000–2004. The emissions growth rate since 2000 was greater than for the most fossil-fuel intensive of the Intergovernmental Panel on Climate Change emissions scenarios developed in the late 1990s. Global emissions growth since 2000 was driven by a cessation or reversal of earlier declining trends in the energy intensity of gross domestic product (GDP) (energy/GDP) and the carbon intensity of energy (emissions/energy), coupled with continuing increases in population and per-capita GDP. Nearly constant or slightly increasing trends in the carbon intensity of energy have been recently observed in both developed and developing regions. No region is decarbonizing its energy supply. The growth rate in emissions is strongest in rapidly developing economies, particularly China. Together, the developing and least-developed economies (forming 80% of the world's population) accounted for 73% of global emissions growth in 2004 but only 41% of global emissions and only 23% of global cumulative emissions since the mid-18th century. The results have implications for global equity. PMID:17519334

Elevated [CO2] magnifies isoprene emissions under heat and improves thermal resistance in hybrid aspen.

PubMed

Sun, Zhihong; Hüve, Katja; Vislap, Vivian; Niinemets, Ülo

2013-12-01

Isoprene emissions importantly protect plants from heat stress, but the emissions become inhibited by instantaneous increase of [CO2], and it is currently unclear how isoprene-emitting plants cope with future more frequent and severe heat episodes under high [CO2]. Hybrid aspen (Populus tremula x Populus tremuloides) saplings grown under ambient [CO2] of 380 μmol mol(-1) and elevated [CO2] of 780 μmol mol(-1) were used to test the hypothesis that acclimation to elevated [CO2] reduces the inhibitory effect of high [CO2] on emissions. Elevated-[CO2]-grown plants had greater isoprene emission capacity and a stronger increase of isoprene emissions with increasing temperature. High temperatures abolished the instantaneous [CO2] sensitivity of isoprene emission, possibly due to removing the substrate limitation resulting from curbed cycling of inorganic phosphate. As a result, isoprene emissions were highest in elevated-[CO2]-grown plants under high measurement [CO2]. Overall, elevated growth [CO2] improved heat resistance of photosynthesis, in particular, when assessed under high ambient [CO2] and the improved heat resistance was associated with greater cellular sugar and isoprene concentrations. Thus, contrary to expectations, these results suggest that isoprene emissions might increase in the future.

Elevated [CO2] magnifies isoprene emissions under heat and improves thermal resistance in hybrid aspen

PubMed Central

Niinemets, Ülo

2013-01-01

Isoprene emissions importantly protect plants from heat stress, but the emissions become inhibited by instantaneous increase of [CO2], and it is currently unclear how isoprene-emitting plants cope with future more frequent and severe heat episodes under high [CO2]. Hybrid aspen (Populus tremula x Populus tremuloides) saplings grown under ambient [CO2] of 380 μmol mol−1 and elevated [CO2] of 780 μmol mol−1 were used to test the hypothesis that acclimation to elevated [CO2] reduces the inhibitory effect of high [CO2] on emissions. Elevated-[CO2]-grown plants had greater isoprene emission capacity and a stronger increase of isoprene emissions with increasing temperature. High temperatures abolished the instantaneous [CO2] sensitivity of isoprene emission, possibly due to removing the substrate limitation resulting from curbed cycling of inorganic phosphate. As a result, isoprene emissions were highest in elevated-[CO2]-grown plants under high measurement [CO2]. Overall, elevated growth [CO2] improved heat resistance of photosynthesis, in particular, when assessed under high ambient [CO2] and the improved heat resistance was associated with greater cellular sugar and isoprene concentrations. Thus, contrary to expectations, these results suggest that isoprene emissions might increase in the future. PMID:24153419

[Spatial temporal differentiation of product-based and consumption-based CO2 emissions and balance in the Beijing-Tianjin-Hebei region: an economic input- output analysis].

PubMed

Wang, Hao; Chen, Cao-cao; Pan, Tao; Liu, Chun-lan; Chen, Long; Sun, Li

2014-09-01

Distinguishing product-based and consumption-based CO2 emissions in the open economic region is the basis for differentiating the emission responsibility, which is attracting increasing attention of decision-makers'attention. The spatial and temporal characteristics of product-based and consumption-based CO2 emissions, as well as carbon balance, in 1997, 2002 and 2007 of JING- JIN-JI region were analyzed by the Economic Input-Output-Life Cycle Assessment model. The results revealed that both the product- based and consumption-based CO2 emissions in the region have been increased by about 4% annually. The percentage of CO2 emissions embodied in trade was 30% -83% , to which the domestic trading added the most. The territorial and consumption-based CO2 emissions in Hebei province were the predominant emission in JING-JIN-JI region, and the increasing speed and emission intensity were stronger than those of Beijing and Tianjin. JING-JIN-JI region was a net inflow region of CO2 emissions, and parts of the emission responsibility were transferred. Beijing and Tianjin were the net importers of CO2 emissions, and Hebei was a net outflow area of CO2 emissions. The key CO2 emission departments in the region were concentrated, and the similarity was great. The inter-regional mechanisms could be set up for joint prevention and control work. - Production and distribution of electricity, gas and water and smelting and pressing of metals had the highest reliability on CO2 emissions, and took on the responsibility of other departments. The EIO-LCA model could be used to analyze the product-based and consumption-based CO2 emissions, which is helpful for the delicate management of regional CO2 emissions reduction and policies making, and stimulating the reduction cooperation at regional scale.

Implications of overestimated anthropogenic CO2 emissions on East Asian and global land CO2 flux inversion

NASA Astrophysics Data System (ADS)

Saeki, Tazu; Patra, Prabir K.

2017-12-01

Measurement and modelling of regional or country-level carbon dioxide (CO2) fluxes are becoming critical for verification of the greenhouse gases emission control. One of the commonly adopted approaches is inverse modelling, where CO2 fluxes (emission: positive flux, sink: negative flux) from the terrestrial ecosystems are estimated by combining atmospheric CO2 measurements with atmospheric transport models. The inverse models assume anthropogenic emissions are known, and thus the uncertainties in the emissions introduce systematic bias in estimation of the terrestrial (residual) fluxes by inverse modelling. Here we show that the CO2 sink increase, estimated by the inverse model, over East Asia (China, Japan, Korea and Mongolia), by about 0.26 PgC year-1 (1 Pg = 1012 g) during 2001-2010, is likely to be an artifact of the anthropogenic CO2 emissions increasing too quickly in China by 1.41 PgC year-1. Independent results from methane (CH4) inversion suggested about 41% lower rate of East Asian CH4 emission increase during 2002-2012. We apply a scaling factor of 0.59, based on CH4 inversion, to the rate of anthropogenic CO2 emission increase since the anthropogenic emissions of both CO2 and CH4 increase linearly in the emission inventory. We find no systematic increase in land CO2 uptake over East Asia during 1993-2010 or 2000-2009 when scaled anthropogenic CO2 emissions are used, and that there is a need of higher emission increase rate for 2010-2012 compared to those calculated by the inventory methods. High bias in anthropogenic CO2 emissions leads to stronger land sinks in global land-ocean flux partitioning in our inverse model. The corrected anthropogenic CO2 emissions also produce measurable reductions in the rate of global land CO2 sink increase post-2002, leading to a better agreement with the terrestrial biospheric model simulations that include CO2-fertilization and climate effects.

Efficiency trends for new commercial jet aircraft 1960-2008

DOT National Transportation Integrated Search

2009-11-01

Concerns about aviations growing climate impact have revived interest in CO2 emission standards for new aircraft. To date, commercial aviation has been perceived to produce continuous improvements in efficiency by quickly adopting fuel-efficient t...

Global Warming in the Twenty-First Century: An Alternative Scenario

NASA Technical Reports Server (NTRS)

Hansen, James; Sato, Makiko; Ruedy, Reto; Lacis, Andrew; Oinas, Valdar; Travis, Larry (Technical Monitor)

2000-01-01

A common view is that the current global warming rate will continue or accelerate. But we argue that rapid warming in recent decades has been driven mainly by non-CO2 greenhouse gases (GHGs), such as chlorofluorocarbons, CH4, and N2O, not by the products of fossil fuel burning, CO2 and aerosols, the positive and negative climate forcings of which are partially offsetting. The growth rate of non-CO2 GHGs has declined in the past decade. If sources of CH4 and O3 precursors were reduced in the future, the change in climate forcing by non-CO2 GHGs in the next 50 years could be near zero. Combined with a reduction of black carbon emissions and plausible success in slowing CO2 emissions, this reduction of non-CO2 GHGs could lead to a decline in the rate of global warming, reducing the danger of dramatic climate change. Such a focus on air pollution has practical benefits that unite the interests of developed and developing countries. However, assessment of ongoing and future climate change requires composition specific long-term global monitoring of aerosol properties.

Global warming in the twenty-first century: an alternative scenario.

PubMed

Hansen, J; Sato, M; Ruedy, R; Lacis, A; Oinas, V

2000-08-29

A common view is that the current global warming rate will continue or accelerate. But we argue that rapid warming in recent decades has been driven mainly by non-CO(2) greenhouse gases (GHGs), such as chlorofluorocarbons, CH(4), and N(2)O, not by the products of fossil fuel burning, CO(2) and aerosols, the positive and negative climate forcings of which are partially offsetting. The growth rate of non-CO(2) GHGs has declined in the past decade. If sources of CH(4) and O(3) precursors were reduced in the future, the change in climate forcing by non-CO(2) GHGs in the next 50 years could be near zero. Combined with a reduction of black carbon emissions and plausible success in slowing CO(2) emissions, this reduction of non-CO(2) GHGs could lead to a decline in the rate of global warming, reducing the danger of dramatic climate change. Such a focus on air pollution has practical benefits that unite the interests of developed and developing countries. However, assessment of ongoing and future climate change requires composition-specific long-term global monitoring of aerosol properties.

Global warming in the twenty-first century: An alternative scenario

PubMed Central

Hansen, James; Sato, Makiko; Ruedy, Reto; Lacis, Andrew; Oinas, Valdar

2000-01-01

A common view is that the current global warming rate will continue or accelerate. But we argue that rapid warming in recent decades has been driven mainly by non-CO2 greenhouse gases (GHGs), such as chlorofluorocarbons, CH4, and N2O, not by the products of fossil fuel burning, CO2 and aerosols, the positive and negative climate forcings of which are partially offsetting. The growth rate of non-CO2 GHGs has declined in the past decade. If sources of CH4 and O3 precursors were reduced in the future, the change in climate forcing by non-CO2 GHGs in the next 50 years could be near zero. Combined with a reduction of black carbon emissions and plausible success in slowing CO2 emissions, this reduction of non-CO2 GHGs could lead to a decline in the rate of global warming, reducing the danger of dramatic climate change. Such a focus on air pollution has practical benefits that unite the interests of developed and developing countries. However, assessment of ongoing and future climate change requires composition-specific long-term global monitoring of aerosol properties. PMID:10944197

Carbon dioxide emission rate of Kīlauea Volcano: Implications for primary magma and the summit reservoir

USGS Publications Warehouse

Gerlach, T.M.; McGee, K.A.; Elias, T.; Sutton, A.J.; Doukas, M.P.

2002-01-01

 We report a CO2 emission rate of 8500 metric tons per day (t d−1) for the summit of Kīlauea Volcano, several times larger than previous estimates. It is based on three sets of measurements over 4 years of synchronous SO2 emission rates and volcanic CO2/SO2concentration ratios for the summit correlation spectrometer (COSPEC) traverse. Volcanic CO2/SO2 for the traverse is representative of the global ratio for summit emissions. The summit CO2 emission rate is nearly constant, despite large temporal variations in summit CO2/SO2 and SO2 emission rates. Summit CO2 emissions comprise most of Kīlauea's total CO2 output (∼9000 t d−1). The bulk CO2 content of primary magma determined from CO2emission and magma supply rate data is ∼0.70 wt %. Most of the CO2 is present as exsolved vapor at summit reservoir depths, making the primary magma strongly buoyant. Turbulent mixing with resident reservoir magma, however, prevents frequent eruptions of buoyant primary magma in the summit region. CO2 emissions confirm that the magma supply enters the edifice through the summit reservoir. A persistent several hundred parts per million CO2 anomaly arises from the entry of magma into the summit reservoir beneath a square kilometer area east of Halemaumau pit crater. Since most of the CO2 in primary magma is degassed in the summit, the summit CO2 emission rate is an effective proxy for the magma supply rate. Both scrubbing of SO2 and solubility controls on CO2and S in basaltic melt cause high CO2/SO2 in summit emissions and spatially uncorrelated distributions of CO2 and SO2 in the summit plume.

The climate response to five trillion tonnes of carbon

NASA Astrophysics Data System (ADS)

Tokarska, Katarzyna B.; Gillett, Nathan P.; Weaver, Andrew J.; Arora, Vivek K.; Eby, Michael

2016-09-01

Concrete actions to curtail greenhouse gas emissions have so far been limited on a global scale, and therefore the ultimate magnitude of climate change in the absence of further mitigation is an important consideration for climate policy. Estimates of fossil fuel reserves and resources are highly uncertain, and the amount used under a business-as-usual scenario would depend on prevailing economic and technological conditions. In the absence of global mitigation actions, five trillion tonnes of carbon (5 EgC), corresponding to the lower end of the range of estimates of the total fossil fuel resource, is often cited as an estimate of total cumulative emissions. An approximately linear relationship between global warming and cumulative CO2 emissions is known to hold up to 2 EgC emissions on decadal to centennial timescales; however, in some simple climate models the predicted warming at higher cumulative emissions is less than that predicted by such a linear relationship. Here, using simulations from four comprehensive Earth system models, we demonstrate that CO2-attributable warming continues to increase approximately linearly up to 5 EgC emissions. These models simulate, in response to 5 EgC of CO2 emissions, global mean warming of 6.4-9.5 °C, mean Arctic warming of 14.7-19.5 °C, and mean regional precipitation increases by more than a factor of four. These results indicate that the unregulated exploitation of the fossil fuel resource could ultimately result in considerably more profound climate changes than previously suggested.

Committed CO2 Emissions of China's Coal-fired Power Plants

NASA Astrophysics Data System (ADS)

Suqin, J.

2016-12-01

The extent of global warming is determined by the cumulative effects of CO2 in the atmosphere. Coal-fired power plants, the largest anthropogenic source of CO2 emissions, produce large amount of CO2 emissions during their lifetimes of operation (committed emissions), which thus influence the future carbon emission space under specific targets on mitigating climate change (e.g., the 2 degree warming limit relative to pre-industrial levels). Comprehensive understanding of committed CO2 emissions for coal-fired power generators is urgently needed in mitigating global climate change, especially in China, the largest global CO2emitter. We calculated China's committed CO2 emissions from coal-fired power generators installed during 1993-2013 and evaluated their impact on future emission spaces at the provincial level, by using local specific data on the newly installed capacities. The committed CO2 emissions are calculated as the product of the annual coal consumption from newly installed capacities, emission factors (CO2emissions per unit crude coal consumption) and expected lifetimes. The sensitivities about generators lifetimes and the drivers on provincial committed emissions are also analyzed. Our results show that these relatively recently installed coal-fired power generators will lead to 106 Gt of CO2 emissions over the course of their lifetimes, which is more than three times the global CO2 emissions from fossil fuels in 2010. More than 80% (85 Gt) of their total committed CO2 will be emitted after 2013, which are referred to as the remaining emissions. Due to the uncertainties of generators lifetime, these remaining emissions would increase by 45 Gt if the lifetimes of China's coal-fired power generators were prolonged by 15 years. Furthermore, the remaining emissions are very different among various provinces owing to local developments and policy disparities. Provinces with large amounts of secondary industry and abundant coal reserves have higher committed emissions. The national and provincial CO2 emission mitigation objectives might be greatly restricted by existing and planned power plants in China. The policy implications of our results have also been discussed.

40 CFR Table 6 to Subpart Zzzz of... - Continuous Compliance With Emission Limitations, Operating Limitations, Work Practices, and...

Code of Federal Regulations, 2012 CFR

2012-07-01

... major source of HAP a. Reduce CO emissions and using an oxidation catalyst, and using a CPMS i... RICE >500 HP located at a major source of HAP a. Reduce CO emissions and not using an oxidation... and using oxidation catalyst or NSCR i. Conducting semiannual performance tests for formaldehyde to...

40 CFR Table 6 to Subpart Zzzz of... - Continuous Compliance With Emission Limitations, Operating Limitations, Work Practices, and...

Code of Federal Regulations, 2011 CFR

2011-07-01

... major source of HAP a. Reduce CO emissions and using an oxidation catalyst, and using a CPMS i... RICE >500 HP located at a major source of HAP a. Reduce CO emissions and not using an oxidation... and using oxidation catalyst or NSCR i. Conducting semiannual performance tests for formaldehyde to...

Observed anomalous changes on diffuse CO2 emission at the summit crater of Teide volcano (Tenerife, Canary Islands, Spain): a geochemical evidence of volcanic unrest?

NASA Astrophysics Data System (ADS)

Perez, N. M.; Melián, G.; Asensio-Ramos, M.; Padrón, E.; Alonso Cótchico, M.; Hernández, P. A.; Rodríguez, F.; D'Auria, L.; García-Merino, M.; Padilla, G. D.; Burns, F.; Amonte, C.; García, E.; García-Hernández, R.; Barrancos, J.; Morales-Ocaña, C.; Calvo, D.; Vela, V.; Pérez, A.

2017-12-01

Tenerife (2034 km2) is the largest of the Canary Islands and hosts a central volcanic complex, Las Cañadas, which is characterized by the eruption of differentiated magmas. Laying inside Las Cañadas a twin stratovolcanoes system Pico Viejo and Teide, has been developed. Although Teide volcano shows weak fumarolic system, volcanic gas emissions observed in the summit area are mainly controlled by high rates of diffuse CO2 degassing. Soil CO2 efflux surveys have been performed at the summit crater of Teide volcano since 1999 according to the accumulation chamber method to monitor changes of volcanic activity. Soil CO2 efflux and soil temperature have been measured in sites homogeneously distributed within an area of about 6,972 m2 inside the summit crater. Historical seismic activity in Tenerife has been mainly characterized by low- to moderate-magnitude events (M <2.5), and most of epicenters clustered in an offshore area SE of Tenerife. Very few earthquakes have occurred in other areas, including Teide volcano. Since November 2016 more than 100 small magnitude earthquakes, with typical features of the microseismicity of hydrothermal systems, at depths usually ranging between 5 and 15 km located beneath Teide volcano have been recorded. On January 6th 2017 a M=2.5 earthquake was recorded in the area, being one of the strongest events recorded since 2004. Between October 11 and December 13, 2016, a continuous increase on the diffuse CO2 emission was registered preceding the occurrence of the 2.5 seismic event, from 21.3±2.0 to 101.7±20.7 t d-1. In Febraury 2017, the diffuse CO2 emission rate showed a maximum value (176±35 t/d) and has remained at relatively high values in the range 67-176 t/d. The observed increase on the diffuse CO2 emission, likely due to the increase of fluid pressure in the hydrothermal-magmatic system of Tenerife, might be a geochemical evidence of a future volcanic unrest at Tenerife Island.

The 2017 Fertilizer Emissions Airborne Study (FEAST): Quantifying N2O emissions from croplands and fertilizer plants in the Mississippi River Valley.

NASA Astrophysics Data System (ADS)

Kort, E. A.; Gvakharia, A.; Smith, M. L.; Conley, S.; Frauhammer, K.

2017-12-01

Nitrous Oxide (N2O) is a crucial atmospheric trace gas that drives 21st century stratospheric ozone depletion and substantively impacts climate. Anthropogenic emissions drive the global imbalance and annual growth of N2O, and the dominant anthropogenic source is fertilizer production and application, both of which have large uncertainties. In this presentation we will discuss the FEAST campaign, a study designed to demonstrate new approaches to quantify N2O emissions from fertilizer production and usage with aircraft measurements. In the FEAST campaign we deployed new instrumentation along with experienced flight sensors onboard the Scientific Aviation Mooney aircraft to make 40 hours of continuous 1Hz measurements of N2O, CO2, CO, H2O, CH4, O3, T, and winds. The Mississippi River Valley provided an optimal target as this location includes significant fertilizer production facilities as well as large cropland areas (dominated by corn, soy, rice, and cotton) with substantive fertilizer application. By leveraging our payload and unique airborne capabilities we directly observe and quantify N2O emissions from individual fertilizer production facilities (as well as CO2 and CH4 emissions from these same facilities). We are also able to quantify N2O fluxes from large cropland areas ( 100's km) employing a mass balance approach, a first for N2O, and will show results highlighting differences between crop types and amounts of applied fertilizer. The ability to quantify fluxes of croplands at 100km scale enables new understanding of processes controlling emissions at spatial scales that has eluded prior studies that either rely on extrapolation of small (flux chamber, towers), or work on 1,000+ km spatial scales (regional-global inversions from atmospheric measurements).

Field Measurements of Particulate Matter Emissions, Carbon Monoxide, and Exhaust Opacity from Heavy-Duty Diesel Vehicles.

PubMed

Clark, Nigel N; Jarrett, Ronald P; Atkinson, Christopher M

1999-09-01

Diesel particulate matter (PM) is a significant contributor to ambient air PM 10 and PM 2.5 particulate levels. In addition, recent literature argues that submicron diesel PM is a pulmonary health hazard. There is difficulty in attributing PM emissions to specific operating modes of a diesel engine, although it is acknowledged that PM production rises dramatically with load and that high PM emissions occur during rapid load increases on turbocharged engines. Snap-acceleration tests generally identify PM associated with rapid transient operating conditions, but not with high load. To quantify the origin of PM during transient engine operation, continuous opacity measurements have been made using a Wager 650CP full flow exhaust opacity meter. Opacity measurements were taken while the vehicles were operated over transient driving cycles on a chassis dynamometer using the West Virginia University (WVU) Transportable Heavy Duty Vehicle Emissions Testing Laboratories. Data were gathered from Detroit Diesel, Cummins, Caterpillar, and Navistar heavy-duty (HD) diesel engines. Driving cycles used were the Central Business District (CBD) cycle, the WVU 5-Peak Truck cycle, the WVU 5-Mile route, and the New York City Bus (NYCB) cycle. Continuous opacity measurements, integrated over the entire driving cycle, were compared to total integrated PM mass. In addition, the truck was subjected to repeat snap-acceleration tests, and PM was collected for a composite of these snap-acceleration tests. Additional data were obtained from a fleet of 1996 New Flyer buses in Flint, MI, equipped with electronically controlled Detroit Diesel Series 50 engines. Again, continuous opacity, regulated gaseous emissions, and PM were measured. The relationship between continuous carbon monoxide (CO) emissions and continuous opacity was noted. In identifying the level of PM emissions in transient diesel engine operation, it is suggested that CO emissions may prove to be a useful indicator and may be used to apportion total PM on a continuous basis over a transient cycle. The projected continuous PM data will prove valuable in future mobile source inventory prediction.

Design and application of a mobile ground-based observatory for continuous measurements of atmospheric trace-gas and criteria pollutant species

NASA Astrophysics Data System (ADS)

Bush, S. E.; Hopkins, F. M.; Randerson, J. T.; Lai, C.-T.; Ehleringer, J. R.

2015-01-01

Ground-based measurements of atmospheric trace gas species and criteria pollutants are essential for understanding emissions dynamics across space and time. Gas composition in the surface 50 m has the greatest direct impacts on human health as well as ecosystem processes, hence data at this level is necessary for addressing carbon cycle and public health related questions. However, such surface data are generally associated with stationary measurement towers, where spatial representation is limited due to the high cost of establishing and maintaining an extensive network of measurement stations. We describe here a compact mobile laboratory equipped to provide high-precision, high-frequency, continuous, on-road synchronous measurements of CO2, CO, CH4, H2O, NOx, O3, aerosol, meteorological, and geospatial position data. The mobile laboratory has been deployed across the western USA. In addition to describing the vehicle and its capacity, we present data that illustrate the use of the laboratory as a powerful tool for investigating the spatial structure of urban trace gas emissions and criteria pollutants at spatial scales ranging from single streets to whole ecosystem and regional scales. We identify fugitive urban CH4 emissions and assess the magnitude of CH4 emissions from known point sources. We illustrate how such a mobile laboratory can be used to better understand emissions dynamics and quantify emissions ratios associated with trace gas emissions from wildfire incidents. Lastly, we discuss additional mobile laboratory applications in health and urban metabolism.

40 CFR 98.193 - Calculating GHG emissions.

Code of Federal Regulations, 2014 CFR

2014-07-01

... (General Stationary Fuel Combustion Sources) the combustion CO2 emissions from each lime kiln according to... must calculate and report the annual process CO2 emissions from all lime kilns combined using the... combustion CO2 emissions from all lime kilns by operating and maintaining a CEMS to measure CO2 emissions...

Carbon dioxide emissions from the electricity sector in major countries: a decomposition analysis.

PubMed

Li, Xiangzheng; Liao, Hua; Du, Yun-Fei; Wang, Ce; Wang, Jin-Wei; Liu, Yanan

2018-03-01

The electric power sector is one of the primary sources of CO 2 emissions. Analyzing the influential factors that result in CO 2 emissions from the power sector would provide valuable information to reduce the world's CO 2 emissions. Herein, we applied the Divisia decomposition method to analyze the influential factors for CO 2 emissions from the power sector from 11 countries, which account for 67% of the world's emissions from 1990 to 2013. We decompose the influential factors for CO 2 emissions into seven areas: the emission coefficient, energy intensity, the share of electricity generation, the share of thermal power generation, electricity intensity, economic activity, and population. The decomposition analysis results show that economic activity, population, and the emission coefficient have positive roles in increasing CO 2 emissions, and their contribution rates are 119, 23.9, and 0.5%, respectively. Energy intensity, electricity intensity, the share of electricity generation, and the share of thermal power generation curb CO 2 emissions and their contribution rates are 17.2, 15.7, 7.7, and 2.8%, respectively. Through decomposition analysis for each country, economic activity and population are the major factors responsible for increasing CO 2 emissions from the power sector. However, the other factors from developed countries can offset the growth in CO 2 emissions due to economic activities.

Relevance of Clean Coal Technology for India’s Energy Security: A Policy Perspective

NASA Astrophysics Data System (ADS)

Garg, Amit; Tiwari, Vineet; Vishwanathan, Saritha

2017-07-01

Climate change mitigation regimes are expected to impose constraints on the future use of fossil fuels in order to reduce greenhouse gas (GHG) emissions. In 2015, 41% of total final energy consumption and 64% of power generation in India came from coal. Although almost a sixth of the total coal based thermal power generation is now super critical pulverized coal technology, the average CO2 emissions from the Indian power sector are 0.82 kg-CO2/kWh, mainly driven by coal. India has large domestic coal reserves which give it adequate energy security. There is a need to find options that allow the continued use of coal while considering the need for GHG mitigation. This paper explores options of linking GHG emission mitigation and energy security from 2000 to 2050 using the AIM/Enduse model under Business-as-Usual scenario. Our simulation analysis suggests that advanced clean coal technologies options could provide promising solutions for reducing CO2 emissions by improving energy efficiencies. This paper concludes that integrating climate change security and energy security for India is possible with a large scale deployment of advanced coal combustion technologies in Indian energy systems along with other measures.

Consumption-based accounting of CO2 emissions

PubMed Central

Davis, Steven J.; Caldeira, Ken

2010-01-01

CO2 emissions from the burning of fossil fuels are the primary cause of global warming. Much attention has been focused on the CO2 directly emitted by each country, but relatively little attention has been paid to the amount of emissions associated with the consumption of goods and services in each country. Consumption-based accounting of CO2 emissions differs from traditional, production-based inventories because of imports and exports of goods and services that, either directly or indirectly, involve CO2 emissions. Here, using the latest available data, we present a global consumption-based CO2 emissions inventory and calculations of associated consumption-based energy and carbon intensities. We find that, in 2004, 23% of global CO2 emissions, or 6.2 gigatonnes CO2, were traded internationally, primarily as exports from China and other emerging markets to consumers in developed countries. In some wealthy countries, including Switzerland, Sweden, Austria, the United Kingdom, and France, >30% of consumption-based emissions were imported, with net imports to many Europeans of >4 tons CO2 per person in 2004. Net import of emissions to the United States in the same year was somewhat less: 10.8% of total consumption-based emissions and 2.4 tons CO2 per person. In contrast, 22.5% of the emissions produced in China in 2004 were exported, on net, to consumers elsewhere. Consumption-based accounting of CO2 emissions demonstrates the potential for international carbon leakage. Sharing responsibility for emissions among producers and consumers could facilitate international agreement on global climate policy that is now hindered by concerns over the regional and historical inequity of emissions. PMID:20212122

The difference of level CO2 emissions from the transportation sector between weekdays and weekend days on the City Centre of Pemalang

NASA Astrophysics Data System (ADS)

Sawitri, E.; Hardiman, G.; Buchori, I.

2017-06-01

The high growth of human activity potentially increases the number of vehicles and the use of fossil fuels that contribute the increase of CO2 emissions in atmosphere. Controlling CO2 emission that causes greenhouse effect becomes the main agenda of Indonesian Government. The first step control CO2 emissions is by measuring the level of CO2 emissions, especially CO2 emissions from fossil fuel consumption in the transport sector. This research aims to assess the level of CO2 emissions from transportation sector on the main roads in the city centre of Pemalang both in weekdays and weekend days. The methods applied to calculate CO2 emissions using Intergovernmental Panel on Climate Change (IPCC) 2006 method. For this, a survey on the number of vehicles passing through the main roads using hand tally counter is firstly done. The results, CO2 emissions in working day, i.e. 49,006.95 tons/year compared to weekend i.e. 38,865.50 tons/year.

Aircraft observations of the urban CO2 dome in London and calculated daytime CO2 fluxes at the urban-regional scale

NASA Astrophysics Data System (ADS)

Font, Anna; Morgui, Josep Anton; Grimmond, Sue; Barratt, Benjamin

2013-04-01

Traffic, industry and energy production and consumption within urban boundaries emit great amounts of CO2 into the atmosphere, creating an urban increment of CO2 mixing ratios compared to the surrounding rural atmosphere. Monitoring CO2 within these 'urban domes' has been proposed as a means to evaluate the effectiveness of policies aiming to mitigate and reduce CO2 urban emissions (CMEGGE, 2010). London is the biggest urban conurbation in Western Europe with more than 8 million inhabitants, and it emitted roughly 45000 ktn CO2 in 2010 (DECC, 2012). In order to develop and implement observational strategies to measure the contribution of urban areas into the global carbon cycle, two airborne surveys were deployed using the Natural and Environment Research Council - Airborne Research and Survey Facility (NERC-ARSF). High frequency measurements of atmospheric CO2, O3, particles and meteorological variables were taken over London in October 2011 and July 2012. CO2 mixing ratios were measured by a Non-Dispersive IR instrument developed by AOS. In July 2012, a Cavity Ring-Down Spectroscopy (CDRS) instrument developed by PICARRO was deployed measuring CO2, CH4 and water vapour at 1Hz resolution. The objectives of the campaigns were to measure the CO2 dome over London and to calculate CO2 emissions at the urban-regional-scale. London was crossed by two transects (SW-NE and SSE-NNW) at an altitude of 360 m and vertical profiles up to 2000 m were carried out to characterize the structure of the atmosphere. Aircraft measurements allowed observation on how CO2 domes were shaped by meteorological conditions. In October 2011, the mean CO2 mixing ratio measured in London was on average 2 ppmv higher than the suburban measurements within the boundary layer. However, under low wind speeds, the CO2 mixing ratio in the urban mixing ratio peaked in central London (>10 ppmv) and decreased towards the city boundaries. Under windy conditions, the structure of the urban dome was dispersed downwind, with peak concentrations displaced from the urban centre along the main wind direction. The urban-regional surface CO2 flux was calculated for four days in October 2011 by either the Integrative Mass Boundary Layer (IMBL) or the Column Integration method (CIM), dependent on meteorological conditions. The diurnal CO2 flux in London obtained from the aircraft observations ranged from 36 to 71 μmol CO2 m-2 s-1 during the day time. This compared well with continuous measurements of CO2 exchange by an eddy-covariance system located in central London. The day-to-day variability observed in the calculated CO2 fluxes responded to the spatial variability of the influence area and emissions that observations were sensitive to. This study provides an example how aircraft surveys in urban areas can be used to estimate CO2 surface fluxes at the urban-regional scale. It also presents an important cross-validation of two independent measurement-based methods to infer the contribution of urban areas to climate change in terms of CO2 emissions that complement bottom-up emissions inventories. References Committee on Methods for Estimating Greenhouse Gas Emissions (2010), The National Academia Press. DECC (2012), http://www.decc.gov.uk/en/content/cms/statistics/indicators/ni186/ni186.aspx

Monitoring trace gases in downtown Toronto using open-path Fourier transform infrared spectroscopy

NASA Astrophysics Data System (ADS)

Byrne, B.; Strong, K.; Colebatch, O.; Fogal, P.; Mittermeier, R. L.; Wunch, D.; Jones, D. B. A.

2017-12-01

Emissions of greenhouse gases (GHGs) in urban environments can be highly heterogeneous. For example, vehicles produce point source emissions which can result in heterogeneous GHG concentrations on scales <10 m. The highly localized scale of these emissions can make it difficult to measure mean GHG concentrations on scales of 100-1000 m. Open-Path Fourier Transform Infrared Spectroscopy (OP-FTIR) measurements offer spatial averaging and continuous measurements of several trace gases simultaneously in the same airmass. We have set up an open-path system in downtown Toronto to monitor trace gases in the urban boundary layer. Concentrations of CO2, CO, CH4, and N2O are derived from atmospheric absorption spectra recorded over a two-way atmospheric open path of 320 m using non-linear least squares fitting. Using a simple box model and co-located boundary layer height measurements, we estimate surface fluxes of these gases in downtown Toronto from our OP-FTIR observations.

MODELING AND MEASUREMENT OF REAL-TIME CO CONCENTRATIONS IN ROADWAY MICROENVIRONMENTS

EPA Science Inventory

Although emission standards for motor vehicles continue to be tightened, tailpipe emissions continue to be a major source of human exposure to air toxics. The United States Environmental protection Agency's national Exposure Research laboratory has initiated a project to impro...

Climate, CO2 and human population impacts on global wildfire emissions

NASA Astrophysics Data System (ADS)

Knorr, W.; Jiang, L.; Arneth, A.

2016-01-01

Wildfires are by far the largest contributor to global biomass burning and constitute a large global source of atmospheric traces gases and aerosols. Such emissions have a considerable impact on air quality and constitute a major health hazard. Biomass burning also influences the radiative balance of the atmosphere and is thus not only of societal, but also of significant scientific interest. There is a common perception that climate change will lead to an increase in emissions as hot and dry weather events that promote wildfire will become more common. However, even though a few studies have found that the inclusion of CO2 fertilisation of photosynthesis and changes in human population patterns will tend to somewhat lower predictions of future wildfire emissions, no such study has included full ensemble ranges of both climate predictions and population projections, including the effect of different degrees of urbanisation.

Here, we present a series of 124 simulations with the LPJ-GUESS-SIMFIRE global dynamic vegetation-wildfire model, including a semi-empirical formulation for the prediction of burned area based on fire weather, fuel continuity and human population density. The simulations use Climate Model Intercomparison Project 5 (CMIP5) climate predictions from eight Earth system models. These were combined with two Representative Concentration Pathways (RCPs) and five scenarios of future human population density based on the series of Shared Socioeconomic Pathways (SSPs) to assess the sensitivity of emissions to the effect of climate, CO2 and humans. In addition, two alternative parameterisations of the semi-empirical burned-area model were applied. Contrary to previous work, we find no clear future trend of global wildfire emissions for the moderate emissions and climate change scenario based on the RCP 4.5. Only historical population change introduces a decline by around 15 % since 1900. Future emissions could either increase for low population growth and fast urbanisation, or continue to decline for high population growth and slow urbanisation. Only for high future climate change (RCP8.5), wildfire emissions start to rise again after ca. 2020 but are unlikely to reach the levels of 1900 by the end of the 21st century. We find that climate warming will generally increase the risk of fire, but that this is only one of several equally important factors driving future levels of wildfire emissions, which include population change, CO2 fertilisation causing woody thickening, increased productivity and fuel load and faster litter turnover in a warmer climate.

Exploring Multiple Constraints of Anthropogenic Pollution

NASA Astrophysics Data System (ADS)

Arellano, A. F., Jr.; Tang, W.; Silva, S. J.; Raman, A.

2017-12-01

It is imperative that we provide more accurate and consistent analysis of anthropogenic pollution emissions at scales that is relevant to air quality, energy, and environmental policy. Here, we present three proof-of-concept studies that explore observational constraints from ground, aircraft, and satellite-derived measurements of atmospheric composition on bulk characteristics of anthropogenic combustion in megacities and fire regions. We focus on jointly analyzing co-emitted combustion products such as CO2, NO2, CO, SO2, and aerosols from GOSAT, OCO-2, OMI, MOPITT, and MODIS retrievals, in conjunction with USEPA AQS and NASA field campaigns. Each of these constituents exhibit distinct atmospheric signatures that depend on fuel type, combustion technology, process, practices and regulatory policies. Our results show that distinguishable patterns and relationships between the increases in concentrations across the megacity (or enhancements) due to emissions of these constituents enable us to: a) identify trends in combustion activity and efficiency, and b) reconcile discrepancies between state- to country-based emission inventories and modeled concentrations of these constituents. For example, the trends in enhancement ratios of these species reveal combustion emission pathways for China and United States that are not captured by current emission inventories and chemical reanalysis. Analysis of their joint distributions has considerable potential utility in current and future integrated constituent data assimilation and inverse modeling activities for monitoring, verifying, and reporting emissions, particularly for regions with few observations and limited information on local combustion processes. This work also motivates the need for continuous and preferably collocated satellite measurements of atmospheric composition, including CH4 and CO2, and studies related to improving the applicability and integration of these observations with ground- and aircraft- based measurements.

What can we learn from field experiments about the development of SOC and GHG emissions under different management practices?

NASA Astrophysics Data System (ADS)

Spiegel, Heide; Lehtinen, Taru; Schlatter, Norman; Haslmayr, Hans-Peter; Baumgarten, Andreas; ten Berge, Hein

2015-04-01

Successful agricultural management practices are required to maintain or enhance soil quality; at the same time climate change mitigation is becoming increasingly important. Within the EU project CATCH-C we analysed the effects of different agricultural practices not only on crop productivity, but also on soil quality indicators (e.g. soil organic carbon (SOC)) and climate change (CC) mitigation indicators (e.g. CO2, CH4, N2O emissions). European data sets and associated literature, mainly from long-term experiments were evaluated. This evaluation of agricultural management practices was carried out comparing a set of improved ("best") and often applied ("current") management practices. Positive and negative effects occurred when best management practices are adopted. As expected, none of the investigated practices could comply with all objectives simultaneously, i.e. maintaining high yields, mitigating climate change and improving chemical, physical and biological soil quality. The studied soil management practices "non-inversion tillage", "organic fertilisation" (application of farm yard manure, slurry, compost) and "incorporation of crop residues" represent important management practices for farmers to increase SOC, thus improving soil quality. However, CO2 and, especially, N2O emissions may rise as well. The evaluation of CC mitigation is often limited by the lack of data from - preferably - continuous GHG emission measurements. Thus, more long-term field studies are needed to better assess the CO2, CH4 and, especially, N2O emissions following the above mentioned favorably rated MPs. Only if SOC and GHG emissions are measured in the same field experiments, it will be possible to compute overall balances of necessary CO2-C equivalent emissions. CATCH-C is funded within the 7th Framework Programme for Research, Technological Development and Demonstration, Theme 2 - Biotechnologies, Agriculture & Food. (Grant Agreement N° 289782).

Prospects for future climate change and the reasons for early action

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

MacCracken, Michael C.

2008-06-15

Combustion of coal, oil, and natural gas, and to a lesser extent deforestation, land-cover change, and emissions of halocarbons and other greenhouse gases, are rapidly increasing the atmospheric concentrations of climate-warming gases. The global average temperature is already approximately 0.8{sup o}C above its preindustrial level, and present atmospheric levels of greenhouse gases will contribute to further warming of 0.5-1{sup o}C as equilibrium is re-established. Warming has been and will be greater in mid and high latitudes compared with low latitudes, over land compared with oceans, and at night compared with day. As emissions continue to increase, both warming and themore » commitment to future warming are presently increasing at a rate of approximately 0.2{sup o}C per decade, with projections that the rate of warming will further increase if emission controls are not put in place. Such warming and the associated changes are likely to result in severe impacts on key societal and environmental support systems. Present estimates are that limiting the increase in global average surface temperature to no more than 2-2.5{sup o}C above its 1750 value of approximately 15{sup o}C will be required to avoid the most catastrophic, but certainly not all, consequences of climate change. Accomplishing this will require reducing emissions sharply by 2050 and to near zero by 2100. This can only be achieved if: (1) developed nations move rapidly to demonstrate that a modem society can function without reliance on technologies that release carbon dioxide (CO{sub 2}) and other non-CO{sub 2} greenhouse gases to the atmosphere; and (2) if developing nations act in the near-term to sharply limit their non-CO{sub 2} emissions while minimizing growth in CO{sub 2} emissions, and then in the long-term join with the developed nations to reduce all emissions as cost-effective technologies are developed. 183 refs., 13 figs., 5 tabs.« less

Outsourcing CO2 Emissions

NASA Astrophysics Data System (ADS)

Davis, S. J.; Caldeira, K. G.

2009-12-01

CO2 emissions from the burning of fossil fuels are the primary cause of global warming. Much attention has been focused on the CO2 directly emitted by each country, but relatively little attention has been paid to the amount of emissions associated with consumption of goods and services in each country. This consumption-based emissions inventory differs from the production-based inventory because of imports and exports of goods and services that, either directly or indirectly, involved CO2 emissions. Using the latest available data and reasonable assumptions regarding trans-shipment of embodied carbon through third-party countries, we developed a global consumption-based CO2 emissions inventory and have calculated associated consumption-based energy and carbon intensities. We find that, in 2004, 24% of CO2 emissions are effectively outsourced to other countries, with much of the developed world outsourcing CO2 emissions to emerging markets, principally China. Some wealthy countries, including Switzerland and Sweden, outsource over half of their consumption-based emissions, with many northern Europeans outsourcing more than three tons of emissions per person per year. The United States is both a big importer and exporter of emissions embodied in trade, outsourcing >2.6 tons of CO2 per person and at the same time as >2.0 tons of CO2 per person are outsourced to the United States. These large flows indicate that CO2 emissions embodied in trade must be taken into consideration when considering responsibility for increasing atmospheric greenhouse gas concentrations.

Eighteen years of geochemical monitoring at the oceanic active volcanic island of El Hierro (Canary Islands, Spain)

NASA Astrophysics Data System (ADS)

Asensio-Ramos, María; Alonso, Mar; Sharp, Emerson; Woods, Hannah; Barrancos, José; Pérez, Nemesio M.

2016-04-01

We report herein the latest results of a diffuse CO2 efflux survey at El Hierro volcanic system carried out during the summer period of 2015 to constrain the total CO2 output from the studied area a during post-eruptive period. El Hierro Island (278 km2) is the youngest and the SW-most of the Canary Islands. On July 16, 2011, a seismic-volcanic crisis started with the occurrence of more than 11,900 seismic events and significant deformation along the island. On October 10, 2011, the dominant character of seismicity changed dramatically from discrete earthquakes to continuous tremor, a clear indication that magma was rapidly approaching the surface immediately before the onset of the eruption, October 12. Eruption was declared over on 5 March, 2012. In order to monitor the volcanic activity of El Hierro Island, from 1998 to 2015 diffuse CO2 emission studies have been performed at El Hierro volcanic system in a yearly basis (˜600 observation sites) according to the accumulation chamber method. Spatial distribution maps were constructed following the sequential Gaussian simulation (sGs) procedure. To quantify the total CO2 emission from the studied area, 100 simulations for each survey have been performed. During the eruption period, soil CO2 efflux values range from non-detectable (˜0.5 g m-2 d-1) up to 457 g m-2 d-1, reaching in November 27, 2011, the maximum CO2 output estimated value of all time series, 2,398 t d-1, just before the episodes of maximum degassing observed as vigorous bubbling at the sea surface and an increment in the amplitude of the tremor signal. During the 2015 survey, soil CO2 efflux values ranged from non-detectable up to 41 g m-2 d-1. The spatial distribution of diffuse CO2 emission values seemed to be controlled by the main volcano structural features of the island. The total diffuse CO2 output released to atmosphere was estimated at 575 ± 24 t d-1, value slightly higher that the background CO2 emission estimated at 422 t d-1 (Melián et al., 2014). The above data demonstrate that discrete surveys of diffuse CO2 emission provide important information to optimize the early warning system in volcano monitoring programs and to monitor the evolution of an ongoing volcanic eruption, even though it is a submarine eruption. References: Melián et al., 2014. J. Geophys. Res. DOI: 10.1002/2014JB011013.

40 CFR 98.83 - Calculating GHG emissions.

Code of Federal Regulations, 2013 CFR

2013-07-01

... (General Stationary Fuel Combustion Sources) the combustion CO2 emissions from the kiln according to the... calculate and report the annual process CO2 emissions from each kiln using the procedure in paragraphs (a... combustion CO2 emissions by operating and maintaining a CEMS to measure CO2 emissions according to the Tier 4...

40 CFR 98.83 - Calculating GHG emissions.

Code of Federal Regulations, 2014 CFR

2014-07-01

... (General Stationary Fuel Combustion Sources) the combustion CO2 emissions from the kiln according to the... calculate and report the annual process CO2 emissions from each kiln using the procedure in paragraphs (a... combustion CO2 emissions by operating and maintaining a CEMS to measure CO2 emissions according to the Tier 4...

40 CFR 98.83 - Calculating GHG emissions.

Code of Federal Regulations, 2012 CFR

2012-07-01

... (General Stationary Fuel Combustion Sources) the combustion CO2 emissions from the kiln according to the... calculate and report the annual process CO2 emissions from each kiln using the procedure in paragraphs (a... combustion CO2 emissions by operating and maintaining a CEMS to measure CO2 emissions according to the Tier 4...

Abundances and Excitation of H2, H3+ & CO in Star-Forming Regions

NASA Astrophysics Data System (ADS)

Kulesa, Craig A.

Although most of the 123 reported interstellar molecules to date have been detected through millimeter-wave emission-line spectroscopy, this technique is inapplicable to non-polar molecules like H2 and H3+, which are central to our understanding of interstellar chemistry. Thus high resolution infrared absorption-line spectroscopy bears an important role in interstellar studies: chemically important non-polar molecules can be observed, and their abundances and excitation conditions can be referred to the same ``pencil beam'' absorbing column. In particular, through a weak quadrupole absorption line spectrum at near-infrared wavelengths, the abundance of cold H2 in dark molecular clouds and star forming regions can now be accurately measured and compared along the same ``pencil beam'' line of sight with the abundance of its most commonly cited surrogate, CO, and its rare isotopomers. Also detected via infrared line absorption is the pivotal molecular ion H3+, whose abundance provides the most direct measurement of the cosmic ray ionization rate in dark molecular clouds, a process that initiates the formation of many other observed molecules there. Our growing sample of H2 and CO detections now includes detailed multi-beam studies of the ρ Ophiuchi molecular cloud and NGC 2024 in Orion. We explore the excitation and degree of ortho- and para-H2 thermalization in dark clouds, variation of the CO abundance over a cloud, and the relation of H2 column density to infrared extinction mapping, far-infrared/submillimeter dust continuum emission, and large scale submillimeter CO, [C I] and HCO+ line emission -- all commonly invoked to indirectly trace H2 during the past 30+ years. For each of the distinct velocity components seen toward some embedded young stellar objects, we are also able to determine the temperature, density, and a CO/H2 abundance ratio, thus unraveling some of the internal structure of a star-forming cloud. H2 and H3+ continue to surprise and delight us with more mysteries. We present imaging and spectroscopy of excited H2 line emission from two Crab Nebula filaments, leading to intriguing questions -- such as the rapid formation, excitation, and continued survival of hydrogen molecules in such a hostile environment. Similarly, we depict the recent detection of CO and H3+ emission from the circumstellar disks of nearby Herbig AeBe stars, providing an outstanding diagnostic of energetic pre-planetary environments and a valuable study of the non-thermal excitation of H3+ in its own right. These studies spotlight the role of molecules as regulators and probes of physical processes in molecular clouds and star- & planet-forming regions. See: http://loke.as.arizona.edu/˜ckulesa/research/ for preprints & more information

Quantifying CO2 Emissions from Individual Power Plants using OCO-2 Observations

NASA Astrophysics Data System (ADS)

Nassar, R.; Hill, T. G.; McLinden, C. A.; Wunch, D.; Jones, D. B. A.; Crisp, D.

2017-12-01

In order to better manage anthropogenic CO2 emissions, improved methods of quantifying emissions are needed at all spatial scales from the national level down to the facility level. Although the Orbiting Carbon Observatory 2 (OCO-2) satellite was not designed for monitoring power plant emissions, we show that in select cases, CO2 observations from OCO-2 can be used to quantify daily CO2 emissions from individual mid- to large-sized coal power plants by fitting the data to plume model simulations. Emission estimates for US power plants are within 1-13% of reported daily emission values enabling application of the approach to international sites that lack detailed emission information. These results affirm that a constellation of future CO2 imaging satellites, optimized for point sources, could be used for the Monitoring, Reporting and Verification (MRV) of CO2 emissions from individual power plants to support the implementation of climate policies.

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

Feldman, Paul D.; A’Hearn, Michael F.; Feaga, Lori M.

ALICE is a far-ultraviolet imaging spectrograph on board Rosetta that, among multiple objectives, is designed to observe emissions from various atomic and molecular species from within the coma of comet 67P/Churyumov–Gerasimenko. The initial observations, made following orbit insertion in 2014 August, showed emissions of atomic hydrogen and oxygen spatially localized close to the nucleus and attributed to photoelectron impact dissociation of H{sub 2}O vapor. Weaker emissions from atomic carbon were subsequently detected and also attributed to electron impact dissociation, of CO{sub 2}, the relative H i and C i line intensities reflecting the variation of CO{sub 2} to H{sub 2}Omore » column abundance along the line of sight through the coma. Beginning in 2015 mid-April, Alice sporadically observed a number of outbursts above the sunward limb characterized by sudden increases in the atomic emissions, particularly the semi-forbidden O i λ 1356 multiplet, over a period of 10–30 minutes, without a corresponding enhancement in long-wavelength solar reflected light characteristic of dust production. A large increase in the brightness ratio O i λ 1356/O i λ 1304 suggests O{sub 2} as the principal source of the additional gas. These outbursts do not correlate with any of the visible images of outbursts taken with either OSIRIS or the navigation camera. Beginning in 2015 June the nature of the Alice spectrum changed considerably with CO Fourth Positive band emission observed continuously, varying with pointing but otherwise fairly constant in time. However, CO does not appear to be a major driver of any of the observed outbursts.« less

Carbon Dioxide Emissions Effects of Grid-Scale Electricity Storage in a Decarbonizing Power System

DOE PAGES

Craig, Michael T.; Jaramillo, Paulina; Hodge, Bri-Mathias

2018-01-03

While grid-scale electricity storage (hereafter 'storage') could be crucial for deeply decarbonizing the electric power system, it would increase carbon dioxide (CO 2) emissions in current systems across the United States. To better understand how storage transitions from increasing to decreasing system CO 2 emissions, we quantify the effect of storage on operational CO 2 emissions as a power system decarbonizes under a moderate and strong CO 2 emission reduction target through 2045. Under each target, we compare the effect of storage on CO 2 emissions when storage participates in only energy, only reserve, and energy and reserve markets. Wemore » conduct our study in the Electricity Reliability Council of Texas (ERCOT) system and use a capacity expansion model to forecast generator fleet changes and a unit commitment and economic dispatch model to quantify system CO 2 emissions with and without storage. We find that storage would increase CO 2 emissions in the current ERCOT system, but would decrease CO 2 emissions in 2025 through 2045 under both decarbonization targets. Storage reduces CO 2 emissions primarily by enabling gas-fired generation to displace coal-fired generation, but also by reducing wind and solar curtailment. We further find that the market in which storage participates drives large differences in the magnitude, but not the direction, of the effect of storage on CO 2 emissions.« less

Carbon Dioxide Emissions Effects of Grid-Scale Electricity Storage in a Decarbonizing Power System

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

Craig, Michael T.; Jaramillo, Paulina; Hodge, Bri-Mathias

While grid-scale electricity storage (hereafter 'storage') could be crucial for deeply decarbonizing the electric power system, it would increase carbon dioxide (CO 2) emissions in current systems across the United States. To better understand how storage transitions from increasing to decreasing system CO 2 emissions, we quantify the effect of storage on operational CO 2 emissions as a power system decarbonizes under a moderate and strong CO 2 emission reduction target through 2045. Under each target, we compare the effect of storage on CO 2 emissions when storage participates in only energy, only reserve, and energy and reserve markets. Wemore » conduct our study in the Electricity Reliability Council of Texas (ERCOT) system and use a capacity expansion model to forecast generator fleet changes and a unit commitment and economic dispatch model to quantify system CO 2 emissions with and without storage. We find that storage would increase CO 2 emissions in the current ERCOT system, but would decrease CO 2 emissions in 2025 through 2045 under both decarbonization targets. Storage reduces CO 2 emissions primarily by enabling gas-fired generation to displace coal-fired generation, but also by reducing wind and solar curtailment. We further find that the market in which storage participates drives large differences in the magnitude, but not the direction, of the effect of storage on CO 2 emissions.« less

Carbon dioxide emissions effects of grid-scale electricity storage in a decarbonizing power system

NASA Astrophysics Data System (ADS)

Craig, Michael T.; Jaramillo, Paulina; Hodge, Bri-Mathias

2018-01-01

While grid-scale electricity storage (hereafter ‘storage’) could be crucial for deeply decarbonizing the electric power system, it would increase carbon dioxide (CO2) emissions in current systems across the United States. To better understand how storage transitions from increasing to decreasing system CO2 emissions, we quantify the effect of storage on operational CO2 emissions as a power system decarbonizes under a moderate and strong CO2 emission reduction target through 2045. Under each target, we compare the effect of storage on CO2 emissions when storage participates in only energy, only reserve, and energy and reserve markets. We conduct our study in the Electricity Reliability Council of Texas (ERCOT) system and use a capacity expansion model to forecast generator fleet changes and a unit commitment and economic dispatch model to quantify system CO2 emissions with and without storage. We find that storage would increase CO2 emissions in the current ERCOT system, but would decrease CO2 emissions in 2025 through 2045 under both decarbonization targets. Storage reduces CO2 emissions primarily by enabling gas-fired generation to displace coal-fired generation, but also by reducing wind and solar curtailment. We further find that the market in which storage participates drives large differences in the magnitude, but not the direction, of the effect of storage on CO2 emissions.

Physical Controls on Carbon Flux from a Temperate Lake During Autumn Cooling

NASA Astrophysics Data System (ADS)

Czikowsky, M. J.; Miller, S. D.; Tedford, E. W.; MacIntyre, S.

2011-12-01

Seasonally-stratified temperate lakes are a source of carbon dioxide to the atmosphere during autumn overturning as CO2 trapped below the thermocline becomes available to the surface for release to the atmosphere. We made continuous measurements of the vertical profile of pCO2 in a ~600 ha temperate lake (Lake Pleasant, maximum depth ~24 m) in southwestern Adirondack Park, New York from mid-September to mid-October 2010 from a moored pontoon boat. Continuous eddy covariance flux measurements of momentum, sensible and latent heat, and CO2 were made in situ, and the water column thermal structure was measured using thermistor chains. The spatial variability (horizontal and vertical) of pCO2 throughout the lake was characterized periodically using a roving profiling system. At the beginning of the study interval, pCO2 at the pontoon boat varied from 500 ppm at the surface to > 3000 ppm below the thermocline. The vertical profile of pCO2 changed markedly during the campaign due to the effects of wind forcing and evaporation (buoyancy), with nearly uniform, high pCO2 throughout the water column at the end of the campaign (Figure 1). The elevated surface water pCO2 increased CO2 emission to the atmosphere.

Evaluating Anthropogenic Carbon Emissions in the Urban Salt Lake Valley through Inverse Modeling: Combining Long-term CO2 Observations and an Emission Inventory using a Multiple-box Atmospheric Model

NASA Astrophysics Data System (ADS)

Catharine, D.; Strong, C.; Lin, J. C.; Cherkaev, E.; Mitchell, L.; Stephens, B. B.; Ehleringer, J. R.

2016-12-01

The rising level of atmospheric carbon dioxide (CO2), driven by anthropogenic emissions, is the leading cause of enhanced radiative forcing. Increasing societal interest in reducing anthropogenic greenhouse gas emissions call for a computationally efficient method of evaluating anthropogenic CO2 source emissions, particularly if future mitigation actions are to be developed. A multiple-box atmospheric transport model was constructed in conjunction with a pre-existing fossil fuel CO2 emission inventory to estimate near-surface CO2 mole fractions and the associated anthropogenic CO2 emissions in the Salt Lake Valley (SLV) of northern Utah, a metropolitan area with a population of 1 million. A 15-year multi-site dataset of observed CO2 mole fractions is used in conjunction with the multiple-box model to develop an efficient method to constrain anthropogenic emissions through inverse modeling. Preliminary results of the multiple-box model CO2 inversion indicate that the pre-existing anthropogenic emission inventory may over-estimate CO2 emissions in the SLV. In addition, inversion results displaying a complex spatial and temporal distribution of urban emissions, including the effects of residential development and vehicular traffic will be discussed.

Mobile laboratory measurements of atmospheric emissions from agriculture, oil, and natural gas activities in northeastern Colorado

NASA Astrophysics Data System (ADS)

Eilerman, S. J.; Peischl, J.; Neuman, J. A.; Ryerson, T. B.; Wild, R. J.; Perring, A. E.; Brown, S. S.; Aikin, K. C.; Holloway, M.; Roberts, O.

2014-12-01

Atmospheric emissions from agriculture are important to air quality and climate, yet their representation in inventories is incomplete. Increased fertilizer use has lead to increased emissions of nitrogen compounds, which can adversely affect ecosystems and contribute to the formation of fine particulates. Furthermore, extraction and processing of oil and natural gas continues to expand throughout northeastern Colorado; emissions from these operations require ongoing measurement and characterization. This presentation summarizes initial data and analysis from a summer 2014 campaign to study emissions of nitrogen compounds, methane, and other species in northeastern Colorado using a new mobile laboratory. A van was instrumented to measure NH3, N2O, NOx, NOy, CH4, CO, CO2, O3, and bioaerosols with high time resolution. By sampling in close proximity to a variety of emissions sources, the mobile laboratory facilitated accurate source identification and quantification of emissions ratios. Measurements were obtained near agricultural sites, natural gas and oil operations, and other point sources. Additionally, extensive measurements were obtained downwind from urban areas and along roadways. The relationship between ammonia and other trace gases is used to characterize sources and constrain emissions inventories.

Satellite Air Quality Monitoring Before, During and After the Beijing 2008 Olympics and Paralympics

NASA Astrophysics Data System (ADS)

Witte, J. C.; Schoeberl, M. R.; Krotkov, N. A.; Pickering, K. E.; Streets, D. G.; Gleason, J. F.; Gille, J. C.

2009-12-01

In 2001, Beijing, China was awarded the hosting rights to the 2008 Olympic and Paralympic Games. Since then, the government has gradually implemented pollution emission control strategies to improve Beijing's air quality in preparation for both games. Long-term industrial and short-term vehicle emission controls have also been enforced upwind of Beijing's neighboring provinces to the south and west. This region is characterized by numerous heavy-polluting industries whose emissions are typically transported towards Beijing, significantly impacting the city's air quality. We examine the efficacy of these emission control measures on tropospheric NO2, SO2, and CO pollution using satellite data from Aura's Ozone Monitoring Instrument (OMI) and Terra's Measurements Of Pollution In The Troposphere (MOPITT) from 2004 to the present. During both games, held in August and September 2008, OMI and MOPITT measured significant decreases in all three tracer gases compared to the past three years: NO2 (-43%), SO2 (-13%), and CO (-12%). This decrease in CO and SO2 over northeastern China continues through 2009, reflecting the longer-term nature of emission controls on heavily polluting industries. The global recession is also a likely contributor, as factories have shut down or slowed production due to the decrease in demand for manufactured goods. The tropospheric NO2 column over Beijing returned to typical monthly mean values when controls on vehicle emissions were lifted by the end of September 2008. However, we observe a slight NO2 decrease at the beginning of 2009 relative to 2008 suggesting a decrease in the contribution of industrial emissions of NOx to the overall NO2 column.

Precursory signals of the 2014-15 Fogo eruption (Cape Verde) detected by surface CO2 emission and heat flow observations

NASA Astrophysics Data System (ADS)

Pérez, Nemesio M.; Dionis, Samara; Fernandes, Paulo; Barrancos, José; Rodríguez, Fátima; Bandomo, Zuleyka; Hernández, Pedro A.; Melián, Gladys V.; Silva, Sónia; Padilla, Germán; Padrón, Eleazar; Cabral, Jeremias; Calvo, David; Asensio-Ramos, María; Pereira, José Manuel; Gonçalves, António A.; Barros, Inocencio; Semedo, Helio

2015-04-01

On November 23, 2014 a new eruption occurred at Fogo volcano (Cape Verde) after 19 years of the last eruptive event in 1995. In the case of the 1995 Fogo eruption, a volcano monitoring program for the volcanic surveillance of Fogo did not exist. On the contrary, a simple and multidisciplinary volcano monitoring program was initiated since 2007 to detect early warning signals of a new volcanic unrest such as the 2014-15 Fogo eruption. Diffuse CO2 emission surveys at the summit crater of Pico do Fogo volcano were periodically carried out from May 2007 to October 2014 to provide this multidisciplinary approach and to monitor potential volcanic activity changes. During this 7 year period, CO2 efflux ranged from non detectable (< 1.5 g m-2 d-1) up to relatively high (61.9 kg m-2 d-1) values. The observed average δ13C- CO2 values related to these diffuse CO2 emission surveys ranged from -22.1 to 1.6 ‰, and surface heat flux measurements, following the method of Dawson (1964), showed also a wide range of values from 0.1 to 460 W m-2. Areas with the highest observed CO2 efflux values were also characterized by a relatively high soil temperature and an intense surface hydrothermal alteration, which supports that degassing process is primary controlled by an advective mechanism generated by geothermal gradients (convection). Two periods of anomalous diffuse CO2 emission were observed between February 2009 to February 2010 and March to August 2014, respectively. Rest of surveys showed the lowest variability on diffuse CO2 emission, ranging from 23 to 186 t d-1 (average = 86 t d-1). The first anomalous period was characterized by a sharp increase on diffuse CO2 emission, suggesting the first magma intrusion beneath Pico do Fogo volcano. This observation is also supported by a significant change on the δ13C- CO2 signature from May 2009 (-10.2 ‰) to February 2010 (-6.1‰) of the diffuse CO2 degassing, indicating an enrichment on the magmatic CO2 component. On February 2010, the diffuse CO2 emission rate was 219 ± 36 t d-1 (Dionis et al., 2015). The second anomalous period started on March 2014, eight months before the 2014-15 Fogo eruption onset, and reached a relatively high value of 337 ± 119 t d-1 on August 30, 2014. It was likely caused by rising of magmatic gases from a second magma intrusion which ended on an eruption. Heat flow temporal evolution during the observation period also shows a quasi-continuous increase before the eruption onset, with the maximum observed heat flow (16.4 ± 3.4 MW) on March 2014. These geochemical and geophysical evidences are clearly precursory signals of the 2014-15 Fogo eruption. Dawson, G.B. (1964), N Z J Geol Geophys 7:155-171; Dionis S. et al. (2015), Bull. Volcanol., in press

New Non-LTE Model of OH and CO2 Emission in the Mesosphere-Lower Thermosphere and its Application to Retrieving Nighttime Parameters

NASA Astrophysics Data System (ADS)

Panka, Peter A.

The hydroxyl, OH, and carbon dioxide, CO2, molecules and oxygen atoms, O(3P), are important parameters that characterize the chemistry, energetics, and dynamics of the nighttime mesosphere and lower thermosphere (MLT) region. Hence, there is much interest in obtaining high quality observations of these parameters in order to study the short-term variability as well as the long-term trends in characteristics of the MLT region. The Sounding of the Atmosphere using Broadband Emission Radiometry (SABER) instrument on board the Thermosphere, Ionosphere, Mesosphere, Energetics, and Dynamics (TIMED) satellite has been taking global, simultaneous measurements of limb infrared radiance in 10 spectral channels, including the OH 2.0 and 1.6-micron and CO2 4.3-micron emissions channels, continuously since late January 2002. These measurements can be interpreted using sophisticated non-Local Thermodynamic Equilibrium (non-LTE) models of OH and CO2 infrared emissions which can then be applied to obtain densities of these parameters (2.0 and 1.6-micron channel for O(3P)/OH and 4.3-micron channel for CO2). The latest non-LTE models of these molecules, however, do not fully represent all the dominant energy transfer mechanisms which influence their vibrational level distributions and infrared emissions. In particular, non-LTE models of CO2 4.3-micron emissions currently under-predict SABER measurements by up to 80%, and its application for the retrieval of CO2 will result in unrealistic densities. Additionally, current O(3P) retrievals from SABER OH emissions have been reported to be at least 30% higher compared to studies using other instruments. Methods to obtain OH total densities from SABER measurements have yet to be developed. Recent studies, however, have discovered a new energy transfer mechanism which influences both OH and CO2 infrared emissions, OH(v) → O(1D) → N2( v) → CO2(v3). This study focuses on the impact of this new mechanism on OH and CO2 infrared emissions as well as model applications for the retrieval of nighttime O( 3P), OH, and CO2 densities. We first study in detail the impact of the new mechanism on OH( v) vibrational level populations and emissions. We compared our calculations with the SABER/TIMED OH 1.6 and 2.0-micron limb radiances of the MLT and with ground and space observations of OH(v) densities in the nighttime mesosphere. We find that the new mechanism produces OH(v) density distributions which are in good agreement with both SABER limb OH emission observations and ground and space measurements. We then couple our OH non-LTE model with CO2 to study the impact of the new mechanism on CO2(v3) vibrational level populations and emissions. We compare our calculations with the SABER/TIMED 4.3-micron CO2 limb radiances and find that the new mechanism provides a strong enhancement of the 4.3-micron CO2 emissions, agreeing to within a 10-30% range. Further, a two-channel retrieval algorithm is developed to self-consistently invert the SABER measured radiances in the OH 2.0 and 1.6-micron channel to obtain vertical profiles of OH and O(3P) Volume Mixing Ratio (VMR). Studies of the inversion algorithm made with synthetic radiances indicate that a stable solution of the inverse problem can be obtained that is nearly independent of the starting conditions. The results presented from the two-channel algorithm to the SABER v2.0 data include comparisons of retrieved O(3P) with current SABER O(3P), in addition to O(3P) retrievals measured by the SCIAMACHY (SCanning Imaging Absorption spectroMeter for Atmospheric CHartographY) instrument, as well as those calculated by the WACCM (Whole Atmosphere Community Climate Model) model for four different days. The O( 3P) density retrieved between 90-95 km are, on average, lower than current SABER O(3P) by 10-50%. OH retrievals are performed over the same days and are compared with OH WACCM calculations as well as other studies. Finally, a similar self-consistent algorithm used for the retrieval of daytime CO2 densities is adopted for nighttime. The situation, however, is more complex for nighttime CO2, where lack of solar irradiation excitation greatly reduce 4.3-micron emission sensitivity to CO 2 density and, therefore, produces unrealistic retrievals. Alternative retrieval methods will be required to overcome these obstacles. For daytime, retrieval of temperature and CO2 are performed simultaneously due to strong coupling between these two parameters. Consideration of this effect will be crucial to obtain accurate nighttime CO2 densities.

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

NASA Technical Reports Server (NTRS)

Lin, Bing

2014-01-01

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

DEVELOPMENT OF A MODEL FOR REAL TIME CO CONCENTRATIONS NEAR ROADWAYS

EPA Science Inventory

Although emission standards for mobile sources continue to be tightened, tailpipe emissions in urban areas continue to be a major source of human exposure to air toxics. Current human exposure models using simplified assumptions based on fixed air monitoring stations and region...

Sampling Singular and Aggregate Point Sources of Carbon Dioxide from Space Using OCO-2

NASA Astrophysics Data System (ADS)

Schwandner, F. M.; Gunson, M. R.; Eldering, A.; Miller, C. E.; Nguyen, H.; Osterman, G. B.; Taylor, T.; O'Dell, C.; Carn, S. A.; Kahn, B. H.; Verhulst, K. R.; Crisp, D.; Pieri, D. C.; Linick, J.; Yuen, K.; Sanchez, R. M.; Ashok, M.

2016-12-01

Anthropogenic carbon dioxide (CO2) sources increasingly tip the natural balance between natural carbon sources and sinks. Space-borne measurements offer opportunities to detect and analyze point source emission signals anywhere on Earth. Singular continuous point source plumes from power plants or volcanoes turbulently mix into their proximal background fields. In contrast, plumes of aggregate point sources such as cities, and transportation or fossil fuel distribution networks, mix into each other and may therefore result in broader and more persistent excess signals of total column averaged CO2 (XCO2). NASA's first satellite dedicated to atmospheric CO2observation, the Orbiting Carbon Observatory-2 (OCO-2), launched in July 2014 and now leads the afternoon constellation of satellites (A-Train). While continuously collecting measurements in eight footprints across a narrow ( < 10 km) wide swath it occasionally cross-cuts coincident emission plumes. For singular point sources like volcanoes and coal fired power plants, we have developed OCO-2 data discovery tools and a proxy detection method for plumes using SO2-sensitive TIR imaging data (ASTER). This approach offers a path toward automating plume detections with subsequent matching and mining of OCO-2 data. We found several distinct singular source CO2signals. For aggregate point sources, we investigated whether OCO-2's multi-sounding swath observing geometry can reveal intra-urban spatial emission structures in the observed variability of XCO2 data. OCO-2 data demonstrate that we can detect localized excess XCO2 signals of 2 to 6 ppm against suburban and rural backgrounds. Compared to single-shot GOSAT soundings which detected urban/rural XCO2differences in megacities (Kort et al., 2012), the OCO-2 swath geometry opens up the path to future capabilities enabling urban characterization of greenhouse gases using hundreds of soundings over a city at each satellite overpass. California Institute of Technology

The right place for the right job in the photovoltaic life cycle.

PubMed

Kawajiri, Kotaro; Genchi, Yutaka

2012-07-03

The potential for photovoltaic power generation (PV) to reduce primary energy consumption (PEC) and CO(2) emissions depends on the physical locations of each stage of its life cycle. When stages are optimally located, CO(2) emissions are reduced nearly ten times as much as when each stage is located in the country having the largest current market share. The usage stage contributes the most to reducing CO(2) emissions and PEC, and total CO(2) emissions actually increase when PV is installed in countries having small CO(2) emissions from electricity generation. Global maps of CO(2) reduction potential indicate that Botswana and Gobi in Mongolia are the optimal locations to install PV due to favorable conditions for PV power generation and high CO(2) emissions from current electricity generation. However, the small electricity demand in those countries limits the contribution to global CO(2) reduction. The type of PVs has a small but significant effect on life cycle PEC and CO(2) emissions.

Regenerable Sorbent for CO2 Removal

NASA Technical Reports Server (NTRS)

Alptekin, Gokhan; Jayaraman, Ambal

2013-01-01

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

Enhanced CO2 uptake at a shallow Arctic Ocean seep field overwhelms the positive warming potential of emitted methane.

PubMed

Pohlman, John W; Greinert, Jens; Ruppel, Carolyn; Silyakova, Anna; Vielstädte, Lisa; Casso, Michael; Mienert, Jürgen; Bünz, Stefan

2017-05-23

Continued warming of the Arctic Ocean in coming decades is projected to trigger the release of teragrams (1 Tg = 10 6 tons) of methane from thawing subsea permafrost on shallow continental shelves and dissociation of methane hydrate on upper continental slopes. On the shallow shelves (<100 m water depth), methane released from the seafloor may reach the atmosphere and potentially amplify global warming. On the other hand, biological uptake of carbon dioxide (CO 2 ) has the potential to offset the positive warming potential of emitted methane, a process that has not received detailed consideration for these settings. Continuous sea-air gas flux data collected over a shallow ebullitive methane seep field on the Svalbard margin reveal atmospheric CO 2 uptake rates (-33,300 ± 7,900 μmol m -2 ⋅d -1 ) twice that of surrounding waters and ∼1,900 times greater than the diffusive sea-air methane efflux (17.3 ± 4.8 μmol m -2 ⋅d -1 ). The negative radiative forcing expected from this CO 2 uptake is up to 231 times greater than the positive radiative forcing from the methane emissions. Surface water characteristics (e.g., high dissolved oxygen, high pH, and enrichment of 13 C in CO 2 ) indicate that upwelling of cold, nutrient-rich water from near the seafloor accompanies methane emissions and stimulates CO 2 consumption by photosynthesizing phytoplankton. These findings challenge the widely held perception that areas characterized by shallow-water methane seeps and/or strongly elevated sea-air methane flux always increase the global atmospheric greenhouse gas burden.

Enhanced CO2 uptake at a shallow Arctic Ocean seep field overwhelms the positive warming potential of emitted methane

PubMed Central

Greinert, Jens; Silyakova, Anna; Vielstädte, Lisa; Casso, Michael; Mienert, Jürgen; Bünz, Stefan

2017-01-01

Continued warming of the Arctic Ocean in coming decades is projected to trigger the release of teragrams (1 Tg = 106 tons) of methane from thawing subsea permafrost on shallow continental shelves and dissociation of methane hydrate on upper continental slopes. On the shallow shelves (<100 m water depth), methane released from the seafloor may reach the atmosphere and potentially amplify global warming. On the other hand, biological uptake of carbon dioxide (CO2) has the potential to offset the positive warming potential of emitted methane, a process that has not received detailed consideration for these settings. Continuous sea−air gas flux data collected over a shallow ebullitive methane seep field on the Svalbard margin reveal atmospheric CO2 uptake rates (−33,300 ± 7,900 μmol m−2⋅d−1) twice that of surrounding waters and ∼1,900 times greater than the diffusive sea−air methane efflux (17.3 ± 4.8 μmol m−2⋅d−1). The negative radiative forcing expected from this CO2 uptake is up to 231 times greater than the positive radiative forcing from the methane emissions. Surface water characteristics (e.g., high dissolved oxygen, high pH, and enrichment of 13C in CO2) indicate that upwelling of cold, nutrient-rich water from near the seafloor accompanies methane emissions and stimulates CO2 consumption by photosynthesizing phytoplankton. These findings challenge the widely held perception that areas characterized by shallow-water methane seeps and/or strongly elevated sea−air methane flux always increase the global atmospheric greenhouse gas burden. PMID:28484018

Development of a hybrid photo-bioreactor and nanoparticle adsorbent system for the removal of CO2, and selected organic and metal co-pollutants.

PubMed

Rocha, Andrea A; Wilde, Christian; Hu, Zhenzhong; Nepotchatykh, Oleg; Nazarenko, Yevgen; Ariya, Parisa A

2017-07-01

Fossil fuel combustion and many industrial processes generate gaseous emissions that contain a number of toxic organic pollutants and carbon dioxide (CO 2 ) which contribute to climate change and atmospheric pollution. There is a need for green and sustainable solutions to remove air pollutants, as opposed to conventional techniques which can be expensive, consume additional energy and generate further waste. We developed a novel integrated bioreactor combined with recyclable iron oxide nano/micro-particle adsorption interfaces, to remove CO 2, and undesired organic air pollutants using natural particles, while generating oxygen. This semi-continuous bench-scale photo-bioreactor was shown to successfully clean up simulated emission streams of up to 45% CO 2 with a conversion rate of approximately 4% CO 2 per hour, generating a steady supply of oxygen (6mmol/hr), while nanoparticles effectively remove several undesired organic by-products. We also showed algal waste of the bioreactor can be used for mercury remediation. We estimated the potential CO 2 emissions that could be captured from our new method for three industrial cases in which, coal, oil and natural gas were used. With a 30% carbon capture system, the reduction of CO 2 was estimated to decrease by about 420,000, 320,000 and 240,000 metric tonnes, respectively for a typical 500MW power plant. The cost analysis we conducted showed potential to scale-up, and the entire system is recyclable and sustainable. We further discuss the implications of usage of this complete system, or as individual units, that could provide a hybrid option to existing industrial setups. Copyright © 2016. Published by Elsevier B.V.

Low-Computation Strategies for Extracting CO2 Emission Trends from Surface-Level Mixing Ratio Observations

NASA Astrophysics Data System (ADS)

Shusterman, A.; Kim, J.; Lieschke, K.; Newman, C.; Cohen, R. C.

2017-12-01

Global momentum is building for drastic, regulated reductions in greenhouse gas emissions over the coming decade. With this increasing regulation comes a clear need for increasingly sophisticated monitoring, reporting, and verification (MRV) strategies capable of enforcing and optimizing emissions-related policy, particularly as it applies to urban areas. Remote sensing and/or activity-based emission inventories can offer MRV insights for entire sectors or regions, but are not yet sophisticated enough to resolve unexpected trends in specific emitters. Urban surface monitors can offer the desired proximity to individual greenhouse gas sources, but due to the densely-packed nature of typical urban landscapes, surface observations are rarely representative of a single source. Most previous efforts to decompose these complex signals into their contributing emission processes have involved inverse atmospheric modeling techniques, which are computationally intensive and believed to depend heavily on poorly understood a priori estimates of error covariance. Here we present a number of transparent, low-computation approaches for extracting source-specific emissions estimates from signals with a variety of nearfield influences. Using observations from the first several years of the BErkeley Atmospheric CO2 Observation Network (BEACO2N), we demonstrate how to exploit strategic pairings of monitoring "nodes," anomalous wind conditions, and well-understood temporal variations to hone in on specific CO2 sources of interest. When evaluated against conventional, activity-based bottom-up emission inventories, these strategies are seen to generate quantitatively rigorous emission estimates. With continued application as the BEACO2N data set grows in time and space, these approaches offer a promising avenue for optimizing greenhouse gas mitigation strategies into the future.

New Model of the night-time CO2 4.3 µm emissions in the mesosphere/lower thermosphere

NASA Astrophysics Data System (ADS)

Panka, P.; Kutepov, A. A.; Kalogerakis, K. S.; Janches, D.; Russell, J. M., III; Rezac, L.; Feofilov, A.; Mlynczak, M. G.; Yiğit, E.

2016-12-01

We present a new non-LTE model of the night-time CO2 4.3 µm emissions in the MLT which accounts for various mechanisms of the non-thermal excitation of CO2 molecules. We pay specific attention to the transfer of vibrational energy of OH(v), produced in the chemical reaction H + O3, to the CO2(v3) vibrational mode. Two energy transfer channels are studied: 1) the "direct" mechanism, OH(v)→N2(v)→CO2(v3)→4.3 µm, suggested by Kumer et al, [1978], and 2) the new "indirect" mechanism, OH(v)→O(1D)→N2(v)→CO2(ν3)→4.3 µm, recently suggested by Sharma et al. [2015]. We show that for various seasonal scenarios above 75 km, the "direct" mechanism alone under-predicts the observed radiance between 30-70%, from 60°S-80°N. However, considering both the "direct" and "indirect" mechanism brings differences between simulated and measured nighttime SABER 4.3 µm limb radiances down to ±10% from 75-85 km and ±20% from 85-110km for the same region. These results suggest that the important mechanism of the nighttime 4.3 µm emission generation, which was missing in previous models [Lopez-Puertas and Taylor, 2001, Lopez-Puertas et al, 2004], has finally been found. This is an important step towards developing the algorithm suitable for retrieving CO2 densities in the MLT from nighttime limb radiances obtained by SABER, which has been taking continuous measurements for the past 15 years.

Direct carbon dioxide emissions from civil aircraft

NASA Astrophysics Data System (ADS)

Grote, Matt; Williams, Ian; Preston, John

2014-10-01

Global airlines consume over 5 million barrels of oil per day, and the resulting carbon dioxide (CO2) emitted by aircraft engines is of concern. This article provides a contemporary review of the literature associated with the measures available to the civil aviation industry for mitigating CO2 emissions from aircraft. The measures are addressed under two categories - policy and legal-related measures, and technological and operational measures. Results of the review are used to develop several insights into the challenges faced. The analysis shows that forecasts for strong growth in air-traffic will result in civil aviation becoming an increasingly significant contributor to anthropogenic CO2 emissions. Some mitigation-measures can be left to market-forces as the key-driver for implementation because they directly reduce airlines' fuel consumption, and their impact on reducing fuel-costs will be welcomed by the industry. Other mitigation-measures cannot be left to market-forces. Speed of implementation and stringency of these measures will not be satisfactorily resolved unattended, and the current global regulatory-framework does not provide the necessary strength of stewardship. A global regulator with ‘teeth' needs to be established, but investing such a body with the appropriate level of authority requires securing an international agreement which history would suggest is going to be very difficult. If all mitigation-measures are successfully implemented, it is still likely that traffic growth-rates will continue to out-pace emissions reduction-rates. Therefore, to achieve an overall reduction in CO2 emissions, behaviour change will be necessary to reduce demand for air-travel. However, reducing demand will be strongly resisted by all stakeholders in the industry; and the ticket price-increases necessary to induce the required reduction in traffic growth-rates place a monetary-value on CO2 emissions of approximately 7-100 times greater than other common valuations. It is clear that, whilst aviation must remain one piece of the transport-jigsaw, environmentally a global regulator with ‘teeth' is urgently required.

First measurements of a carbon dioxide plume from an industrial source using a ground based mobile differential absorption lidar.

PubMed

Robinson, R A; Gardiner, T D; Innocenti, F; Finlayson, A; Woods, P T; Few, J F M

2014-08-01

The emission of carbon dioxide (CO2) from industrial sources is one of the main anthropogenic contributors to the greenhouse effect. Direct remote sensing of CO2 emissions using optical methods offers the potential for the identification and quantification of CO2 emissions. We report the development and demonstration of a ground based mobile differential absorption lidar (DIAL) able to measure the mass emission rate of CO2 in the plume from a power station. To our knowledge DIAL has not previously been successfully applied to the measurement of emission plumes of CO2 from industrial sources. A significant challenge in observing industrial CO2 emission plumes is the ability to discriminate and observe localised concentrations of CO2 above the locally observed background level. The objectives of the study were to modify our existing mobile infrared DIAL system to enable CO2 measurements and to demonstrate the system at a power plant to assess the feasibility of the technique for the identification and quantification of CO2 emissions. The results of this preliminary study showed very good agreement with the expected emissions calculated by the site. The detection limit obtained from the measurements, however, requires further improvement to provide quantification of smaller emitters of CO2, for example for the detection of fugitive emissions. This study has shown that in principle, remote optical sensing technology will have the potential to provide useful direct data on CO2 mass emission rates.

Constraining East Asian CO2 emissions with GOSAT retrievals: methods and policy implications

NASA Astrophysics Data System (ADS)

Shim, C.; Henze, D. K.; Deng, F.

2017-12-01

The world largest CO2 emissions are from East Asia. However, there are large uncertainties in CO2 emission inventories, mainly because of imperfections in bottom-up statistics and a lack of observations for validating emission fluxes, particularly over China. Here we tried to constrain East Asian CO2 emissions with GOSAT retrievals applying 4-Dvar GEOS-Chem and its adjoint model. We applied the inversion to only the cold season (November - February) in 2009 - 2010 since the summer monsoon and greater transboundary impacts in spring and fall greatly reduced the GOSAT retrievals. In the cold season, the a posteriori CO2 emissions over East Asia generally higher by 5 - 20%, particularly Northeastern China shows intensively higher in a posteriori emissions ( 20%), where the Chinese government is recently focusing on mitigating the air pollutants. In another hand, a posteriori emissions from Southern China are lower 10 - 25%. A posteriori emissions in Korea and Japan are mostly higher by 10 % except over Kyushu region. With our top-down estimates with 4-Dvar CO2 inversion, we will evaluate the current regional CO2 emissions inventories and potential uncertainties in the sectoral emissions. This study will help understand the quantitative information on anthropogenic CO2 emissions over East Asia and will give policy implications for the mitigation targets.

The impacts of non-renewable and renewable energy on CO2 emissions in Turkey.

PubMed

Bulut, Umit

2017-06-01

As a result of great increases in CO 2 emissions in the last few decades, many papers have examined the relationship between renewable energy and CO 2 emissions in the energy economics literature, because as a clean energy source, renewable energy can reduce CO 2 emissions and solve environmental problems stemming from increases in CO 2 emissions. When one analyses these papers, he/she will observe that they employ fixed parameter estimation methods, and time-varying effects of non-renewable and renewable energy consumption/production on greenhouse gas emissions are ignored. In order to fulfil this gap in the literature, this paper examines the effects of non-renewable and renewable energy on CO 2 emissions in Turkey over the period 1970-2013 by employing fixed parameter and time-varying parameter estimation methods. Estimation methods reveal that CO 2 emissions are positively related to non-renewable energy and renewable energy in Turkey. Since policy makers expect renewable energy to decrease CO 2 emissions, this paper argues that renewable energy is not able to satisfy the expectations of policy makers though fewer CO 2 emissions arise through production of electricity using renewable sources. In conclusion, the paper argues that policy makers should implement long-term energy policies in Turkey.

Financial development and sectoral CO2 emissions in Malaysia.

PubMed

Maji, Ibrahim Kabiru; Habibullah, Muzafar Shah; Saari, Mohd Yusof

2017-03-01

The paper examines the impacts of financial development on sectoral carbon emissions (CO 2 ) for environmental quality in Malaysia. Since the financial sector is considered as one of the sectors that will contribute to Malaysian economy to become a developed country by 2020, we utilize a cointegration method to investigate how financial development affects sectoral CO 2 emissions. The long-run results reveal that financial development increases CO 2 emissions from the transportation and oil and gas sector and reduces CO 2 emissions from manufacturing and construction sectors. However, the elasticity of financial development is not significant in explaining CO 2 emissions from the agricultural sector. The results for short-run elasticities were also consistent with the long-run results. We conclude that generally, financial development increases CO 2 emissions and reduces environmental quality in Malaysia.

Non-CO2 Greenhouse Gas Emissions in China 2012: Inventory and Supply Chain Analysis

NASA Astrophysics Data System (ADS)

Zhang, Bo; Zhang, Yaowen; Zhao, Xueli; Meng, Jing

2018-01-01

Reliable inventory information is critical in informing emission mitigation efforts. Using the latest officially released emission data, which is production based, we take a consumption perspective to estimate the non-CO2 greenhouse gas (GHG) emissions for China in 2012. The non-CO2 GHG emissions, which cover CH4, N2O, HFCs, PFCs, and SF6, amounted to 2003.0 Mt. CO2-eq (including 1871.9 Mt. CO2-eq from economic activities), much larger than the total CO2 emissions in some developed countries. Urban consumption (30.1%), capital formation (28.2%), and exports (20.6%) derived approximately four fifths of the total embodied emissions in final demand. Furthermore, the results from structural path analysis help identify critical embodied emission paths and key economic sectors in supply chains for mitigating non-CO2 GHG emissions in Chinese economic systems. The top 20 paths were responsible for half of the national total embodied emissions. Several industrial sectors such as Construction, Production and Supply of Electricity and Steam, Manufacture of Food and Tobacco and Manufacture of Chemicals, and Chemical Products played as the important transmission channels. Examining both production- and consumption-based non-CO2 GHG emissions will enrich our understanding of the influences of industrial positions, final consumption demands, and trades on national non-CO2 GHG emissions by considering the comprehensive abatement potentials in the supply chains.

Climate, CO2, and demographic impacts on global wildfire emissions

NASA Astrophysics Data System (ADS)

Knorr, W.; Jiang, L.; Arneth, A.

2015-09-01

Wildfires are by far the largest contributor to global biomass burning and constitute a large global source of atmospheric traces gases and aerosols. Such emissions have a considerable impact on air quality and constitute a major health hazard. Biomass burning also influences the radiative balance of the atmosphere and is thus not only of societal, but also of significant scientific interest. There is a common perception that climate change will lead to an increase in emissions as hot and dry weather events that promote wildfire will become more common. However, even though a few studies have found that the inclusion of CO2 fertilization of photosynthesis and changes in human population patterns will tend to somewhat lower predictions of future wildfire emissions, no such study has included full ensemble ranges of both climate predictions and population projections, including the effect of different degrees of urbanisation. Here, we present a series of 124 simulations with the LPJ-GUESS-SIMFIRE global dynamic vegetation - wildfire model, including a semi-empirical formulation for the prediction of burned area based on fire weather, fuel continuity and human population density. The simulations comprise Climate Model Intercomparison Project 5 (CMIP5) climate predictions from eight Earth system models using two Representative Concentration Pathways (RCPs) and five scenarios of future human population density based on the series of Shared Socioeconomic Pathways (SSPs), sensitivity tests for the effect of climate and CO2, as well as a sensitivity analysis using two alternative parameterisations of the semi-empirical burned-area model. Contrary to previous work, we find no clear future trend of global wildfire emissions for the moderate emissions and climate change scenario based on the RCP 4.5. Only historical population change introduces a decline by around 15 % since 1900. Future emissions could either increase for low population growth and fast urbanisation, or continue to decline for high population growth and slow urbanisation. Only for high future climate change (RCP8.5), wildfire emissions start to rise again after ca. 2020 but are unlikely to reach the levels of 1900 by the end of the 21st century. We find that climate warming will generally increase the risk of fire, but that this is only one of several equally important factors driving future levels of wildfire emissions, which include population change, CO2 fertilisation causing woody thickening, increased productivity and fuel load, and faster litter turnover in a warmer climate.

RESULTS OF THE SEPTEMBER 1997 DOE/EPA DEMONSTRATION OF MULTIMETAL CONTINUOUS EMISSION MONITORING TECHNOLOGIES

EPA Science Inventory

In September 1997, the U.S. Department of Energy (DOE) and U.S. Environmental Protection Agency (EPA) co-sponsored a demonstration of several multimetal continuous emission monitos (CEMs). The demonstration, performed at the EPA National Risk Management Research Laboratory, Air P...

First field determination of the 13C/12C isotope ratio in volcanic CO2 by diode-laser.

PubMed

Castrillo, A; Casa, G; van Burgel, M; Tedesco, D; Gianfrani, L

2004-12-27

Carbon isotope ratio analysis using a laser-based technique has been performed in the field, on the gaseous emissions from an active volcano. We here describe that 13CO2/12CO2 determinations can be carried out in a quasi-continuous regime using a compact, selective and sensitive diode laser spectrometer at a wavelength of 2 mum. Within the Solfatara crater (near Naples, Italy), in a very harsh environment, we were able to determine relative 13CO2/12CO2 values, on the highest flux fumarole, with an accuracy of 0.5 per thousand. Regular and frequent observations of the carbon isotopes in volcanic gases, which become possible with our methodology, are of the utmost importance for geochemical surveillance of volcanoes.

Multidecadal Increase in North Atlantic Coccolithophores and Potential Role of Increasing CO2

NASA Astrophysics Data System (ADS)

Rivero-Calle, S.; Gnanadesikan, A.; del Castillo, C. E.; Balch, W. M.; Guikema, S.

2016-02-01

As anthropogenic CO2 emissions acidify the oceans, calcifiers are expected to be negatively impacted. Using data from the Continuous Plankton Recorder, we show that coccolithophore occurrence in the North Atlantic has increased from 2 to over 20% from 1965 through 2010. We used Random Forest models to examine more than 20 possible environmental drivers of this change. CO2 and the Atlantic Multidecadal Oscillation were the best predictors. Since coccolithophore photosynthesis is strongly carbon-limited, we hypothesize that higher CO2 levels might be encouraging growth. A compilation of 41 independent laboratory studies supports our hypothesis. Our study shows a long-term basin-scale increase in coccolithophores and suggests that increasing pCO2 and temperature accelerated the growth rate of a key phytoplankton group for carbon cycling.

An ensemble approach to simulate CO2 emissions from natural fires

NASA Astrophysics Data System (ADS)

Eliseev, A. V.; Mokhov, I. I.; Chernokulsky, A. V.

2014-01-01

This paper presents ensemble simulations with the global climate model developed at the A. M. Obukhov Institute of Atmospheric Physics, Russian Academy of Sciences (IAP RAS CM). These simulations were forced by historical reconstruction of external forcings for 850-2005 AD and by the Representative Concentration Pathways (RCP) scenarios till year 2300. Different ensemble members were constructed by varying the governing parameters of the IAP RAS CM module to simulate natural fires. These members are constrained by the GFED-3.1 observational data set and further subjected to Bayesian averaging. This approach allows to select only changes in fire characteristics which are robust within the constrained ensemble. In our simulations, the present-day (1998-2011 AD) global area burnt due to natural fires is (2.1 ± 0.4) × 106 km2 yr-1 (ensemble means and intra-ensemble standard deviations are presented), and the respective CO2 emissions in the atmosphere are (1.4 ± 0.2) PgC yr-1. The latter value is in agreement with the corresponding observational estimates. Regionally, the model underestimates CO2 emissions in the tropics; in the extra-tropics, it underestimates these emissions in north-east Eurasia and overestimates them in Europe. In the 21st century, the ensemble mean global burnt area is increased by 13% (28%, 36%, 51%) under scenario RCP 2.6 (RCP 4.5, RCP 6.0, RCP 8.5). The corresponding global emissions increase is 14% (29%, 37%, 42%). In the 22nd-23rd centuries, under the mitigation scenario RCP 2.6 the ensemble mean global burnt area and respective CO2 emissions slightly decrease, both by 5% relative to their values in year 2100. Under other RCP scenarios, these variables continue to increase. Under scenario RCP 8.5 (RCP 6.0, RCP 4.5) the ensemble mean burnt area in year 2300 is higher by 83% (44%, 15%) than its value in year 2100, and the ensemble mean CO2 emissions are correspondingly higher by 31% (19%, 9%). All changes of natural fire characteristics in the 21st-23rd centuries are associated mostly with the corresponding changes in boreal regions of Eurasia and North America. However, under the RCP 8.5 scenario, increase of the burnt area and CO2 emissions in boreal regions during the 22nd-23rd centuries are accompanied by the respective decreases in the tropics and subtropics.

Greenhouse gas emissions from on-site wastewater treatment systems

NASA Astrophysics Data System (ADS)

Somlai-Haase, Celia; Knappe, Jan; Gill, Laurence

2016-04-01

Nearly one third of the Irish population relies on decentralized domestic wastewater treatment systems which involve the discharge of effluent into the soil via a percolation area (drain field). In such systems, wastewater from single households is initially treated on-site either by a septic tank and an additional packaged secondary treatment unit, in which the influent organic matter is converted into carbon dioxide (CO2) and methane (CH4) by microbial mediated processes. The effluent from the tanks is released into the soil for further treatment in the unsaturated zone where additional CO2 and CH4 are emitted to the atmosphere as well as nitrous oxide (N2O) from the partial denitrification of nitrate. Hence, considering the large number of on-site systems in Ireland and internationally, these are potential significant sources of greenhouse gas (GHG) emissions, and yet have received almost no direct field measurement. Here we present the first attempt to quantify and qualify the production and emissions of GHGs from a septic tank system serving a single house in the County Westmeath, Ireland. We have sampled the water for dissolved CO2, CH4 and N2O and measured the gas flux from the water surface in the septic tank. We have also carried out long-term flux measurements of CO2 from the drain field, using an automated soil gas flux system (LI-8100A, Li-Cor®) covering a whole year semi-continuously. This has enabled the CO2 emissions from the unsaturated zone to be correlated against different meteorological parameters over an annual cycle. In addition, we have integrated an ultraportable GHG analyser (UGGA, Los Gatos Research Inc.) into the automated soil gas flux system to measure CH4 flux. Further, manual sampling has also provided a better understanding of N2O emissions from the septic tank system.

CO2 Degassing at Kilauea Volcano: Implications for Primary Magma, Summit Reservoir Dynamics, and Magma Supply Monitoring

NASA Astrophysics Data System (ADS)

Gerlach, T. M.; McGee, K. A.; Elias, T.; Sutton, A. J.; Doukas, M. P.

2001-12-01

We report a new CO2 emission rate of 8,500 tons/day (t/d) for the summit of Kilauea Volcano, a result several times larger than previous estimates. It is based on 12 experiments on three occasions over four years constraining the SO2 emission rate and the average CO2/SO2 of emissions along the 5.4-km summit COSPEC traverse (by COSPEC, NDIR CO2 analyzer, and CP-FTIR). The core of the summit plume is at ground level along the traverse and gives average CO2/SO2 values that are representative of the overall summit emission, even though CO2 and SO2 variations are commonly uncorrelated. CO2 and SO2 concentrations exceed background by 200-1,000 ppm and 1-7 ppm respectively. Nighttime measurements exclude Park auto exhaust as a source of CO2. The summit CO2 emission rate is nearly constant (95% confidence interval = 300 t/d), despite variable summit SO2 emission rates (62-240 t/d) and CO2/SO2 (54-183). Including other known CO2 emissions on the volcano (mainly from the Pu`u `O`o eruption) gives a total emission rate of about 8,800 t/d. Thus summit CO2 emissions comprise 97% of the total known CO2 output, consistent with the hypothesis that all primary magma supplied to Kilauea arrives under the summit caldera and is thoroughly degassed of excess CO2. A persistent large CO2 anomaly of 200-1,000 ppm indicates the entry to the summit reservoir is beneath a km2-area east of Halemaumau. The bulk CO2 content of primary magma is about 0.70 wt%, inferred from the CO2 emission rate and Kilauea's magma supply rate (0.18 km3/y [Cayol et al., Science, 288, 2343, 2000]). Most of the CO2 is present as exsolved vapor (3.6-11.7 vol%) at summit reservoir depths (2-7 km), making the primary magma strongly buoyant. Magma chamber replenishment models show that robust turbulent mixing of primary and reservoir magma prevents frequent eruption of buoyant primary magma in the summit region. The escape of 90-95% of the CO2 from the summit reservoir provides a potential proxy for monitoring the magma supply rate. Streaming CO2-rich vapor causes fractional degassing of H2O and SO2 from reservoir magma, but scrubbing minimizes summit SO2 emissions.

The Hestia Project: High Spatial Resolution Fossil Fuel Carbon Dioxide Emissions Quantification at Hourly Scale in Indianapolis, USA

NASA Astrophysics Data System (ADS)

Zhou, Y.; Gurney, K. R.

2009-12-01

In order to advance the scientific understanding of carbon exchange with the land surface and contribute to sound, quantitatively-based U.S. climate change policy interests, quantification of greenhouse gases emissions drivers at fine spatial and temporal scales is essential. Quantification of fossil fuel CO2 emissions, the primary greenhouse gases, has become a key component to cost-effective CO2 emissions mitigation options and a carbon trading system. Called the ‘Hestia Project’, this pilot study generated CO2 emissions down to high spatial resolution and hourly scale for the greater Indianapolis region in the USA through the use of air quality and traffic monitoring data, remote sensing, GIS, and building energy modeling. The CO2 emissions were constructed from three data source categories: area, point, and mobile. For the area source emissions, we developed an energy consumption model using DOE/EIA survey data on building characteristics and energy consumption. With the Vulcan Project’s county-level CO2 emissions and simulated building energy consumption, we quantified the CO2 emissions for each individual building by allocating Vulcan emissions to roughly 50,000 structures in Indianapolis. The temporal pattern of CO2 emissions in each individual building was developed based on temporal patterns of energy consumption. The point sources emissions were derived from the EPA National Emissions Inventory data and effluent monitoring of electricity producing facilities. The mobile source CO2 emissions were estimated at the month/county scale using the Mobile6 combustion model and the National Mobile Inventory Model database. The month/county scale mobile source CO2 emissions were downscaled to the “native” spatial resolution of road segments every hour using a GIS road atlas and traffic monitoring data. The result is shown in Figure 1. The resulting urban-scale inventory can serve as a baseline of current CO2 emissions and should be of immediate use to city environmental managers and regional industry as they plan emission mitigation options and project future emission trends. The results obtained here will also be a useful comparison to atmospheric CO2 monitoring efforts from the top-down. Figure 1. Location of the study area, the building level and mobile CO2 emissions, and an enlarged example neighborhood

Predictive NO x emission monitoring on board a passenger ferry

NASA Astrophysics Data System (ADS)

Cooper, D. A.; Andreasson, K.

NO x emissions from a medium speed diesel engine on board a servicing passenger ferry have been indirectly measured using a predictive emission monitoring system (PEMS) over a 1-yr period. Conventional NO x measurements were carried out with a continuous emission monitoring system (CEMS) at the start of the study to provide historical data for the empirical PEMS function. On three other occasions during the year the CEMS was also used to verify the PEMS and follow any changes in emission signature of the engine. The PEMS consisted of monitoring exhaust O 2 concentrations (in situ electrochemical probe), engine load, combustion air temperature and humidity, and barometric pressure. Practical experiences with the PEMS equipment were positive and measurement data were transferred to a land-based office by using a modem data communication system. The initial PEMS function (PEMS1) gave systematic differences of 1.1-6.9% of the calibration domain (0-1725 ppm) and a relative accuracy of 6.7% when compared with CEMS for whole journeys and varying load situations. Further improvements on the performance could be obtained by updating this function. The calculated yearly emission for a total engine running time of 4618 h was 316 t NO x±38 t and the average NO x emission corrected for ambient conditions 14.3 g kWh corr-1. The exhaust profile of the engine in terms of NO x, CO and CO 2 emissions as determined by CEMS was similar for most of the year. Towards the end of the study period, a significantly lower NO x emission was detected which was probably caused by replacement of fuel injector nozzles. The study suggests that PEMS can be a viable option for continuous, long-term NO x measurements on board ships.

Energy-dominated local carbon emissions in Beijing 2007: inventory and input-output analysis.

PubMed

Guo, Shan; Liu, J B; Shao, Ling; Li, J S; An, Y R

2012-01-01

For greenhouse gas (GHG) emissions by Beijing economy 2007, a concrete emission inventory covering carbon dioxide (CO(2)), methane (CH(4)), and nitrous oxide (N(2)O) is presented and associated with an input-output analysis to reveal the local GHG embodiment in final demand and trade without regard to imported emissions. The total direct GHG emissions amount to 1.06E + 08 t CO(2)-eq, of which energy-related CO(2) emissions comprise 90.49%, non-energy-related CO(2) emissions 6.35%, CH(4) emissions 2.33%, and N(2)O emissions 0.83%, respectively. In terms of energy-related CO(2) emissions, the largest source is coal with a percentage of 53.08%, followed by coke with 10.75% and kerosene with 8.44%. Sector 26 (Construction Industry) holds the top local emissions embodied in final demand of 1.86E + 07 t CO(2)-eq due to its considerable capital, followed by energy-intensive Sectors 27 (Transport and Storage) and 14 (Smelting and Pressing of Ferrous and Nonferrous Metals). The GHG emissions embodied in Beijing's exports are 4.90E + 07 t CO(2)-eq, accounting for 46.01% of the total emissions embodied in final demand. The sound scientific database totally based on local emissions is an important basis to make effective environment and energy policies for local decision makers.

Energy-Dominated Local Carbon Emissions in Beijing 2007: Inventory and Input-Output Analysis

PubMed Central

Guo, Shan; Liu, J. B.; Shao, Ling; Li, J. S.; An, Y. R.

2012-01-01

For greenhouse gas (GHG) emissions by Beijing economy 2007, a concrete emission inventory covering carbon dioxide (CO2), methane (CH4), and nitrous oxide (N2O) is presented and associated with an input-output analysis to reveal the local GHG embodiment in final demand and trade without regard to imported emissions. The total direct GHG emissions amount to 1.06E + 08 t CO2-eq, of which energy-related CO2 emissions comprise 90.49%, non-energy-related CO2 emissions 6.35%, CH4 emissions 2.33%, and N2O emissions 0.83%, respectively. In terms of energy-related CO2 emissions, the largest source is coal with a percentage of 53.08%, followed by coke with 10.75% and kerosene with 8.44%. Sector 26 (Construction Industry) holds the top local emissions embodied in final demand of 1.86E + 07 t CO2-eq due to its considerable capital, followed by energy-intensive Sectors 27 (Transport and Storage) and 14 (Smelting and Pressing of Ferrous and Nonferrous Metals). The GHG emissions embodied in Beijing's exports are 4.90E + 07 t CO2-eq, accounting for 46.01% of the total emissions embodied in final demand. The sound scientific database totally based on local emissions is an important basis to make effective environment and energy policies for local decision makers. PMID:23193385

Improved attribution of climate forcing to emissions by pollutant and sector

NASA Astrophysics Data System (ADS)

Shindell, D. T.

2009-12-01

Evaluating multi-component climate change mitigation strategies requires knowledge of the diverse direct and indirect effects of emissions. Methane, ozone and aerosols are linked through atmospheric chemistry so that emissions of a single pollutant can affect several species. I will show new calculations of atmospheric composition changes, radiative forcing, and the global warming potential (GWP) for increased emissions of tropospheric ozone and aerosol precursors in a coupled composition-climate model. The results demonstrate that gas-aerosol interactions substantially alter the relative importance of the various emissions, suggesting revisions to the GWPs used in international carbon trading. Additionally, I will present results showing how the net climate impact of particular activities depends strongly upon non-CO2 forcing agents for some sectors. These results will be highlighted by discussing the interplay between air quality emissions controls and climate for the case of emissions from coal-fired power plants. The changing balance between CO2 and air quality pollutants from coal plants may have contributed to the 20th century spatial and temporal patterns of climate change, and is likely to continue to do so as more and more plants are constructed in Asia.

40 CFR 75.19 - Optional SO 2, NO X, and CO 2 emissions calculation for low mass emissions (LME) units.

Code of Federal Regulations, 2013 CFR

2013-07-01

... 40 Protection of Environment 17 2013-07-01 2013-07-01 false Optional SO 2, NO X, and CO 2... Provisions § 75.19 Optional SO 2, NO X, and CO 2 emissions calculation for low mass emissions (LME) units. (a...) Determination of SO 2, NO X, and CO 2 emission rates. (i) If the unit combusts only natural gas and/or fuel oil...

40 CFR 75.19 - Optional SO 2, NO X, and CO 2 emissions calculation for low mass emissions (LME) units.

Code of Federal Regulations, 2014 CFR

2014-07-01

... 40 Protection of Environment 17 2014-07-01 2014-07-01 false Optional SO 2, NO X, and CO 2... Provisions § 75.19 Optional SO 2, NO X, and CO 2 emissions calculation for low mass emissions (LME) units. (a...) Determination of SO 2, NO X, and CO 2 emission rates. (i) If the unit combusts only natural gas and/or fuel oil...

Annual Greenhouse Gas (CO2, CH4, and N2O) Fluxes Via Ebullition from a Temperate Emergent Wetland

NASA Astrophysics Data System (ADS)

Mcnicol, G.; Sturtevant, C. S.; Knox, S. H.; Baldocchi, D. D.; Silver, W. L.

2014-12-01

Quantifying wetland greenhouse gas exchange is necessary to evaluate their potential for mitigating climate change via carbon sequestration. However measuring greenhouse gas fluxes of carbon dioxide (CO2), methane (CH4), and nitrous oxide (N2O) in wetlands is difficult due to high spatial and temporal variability, and multiple transport pathways of emission. Transport of biogenic soil gas via highly sporadic ebullition (bubbling) events is often ignored or quantified poorly in wetland greenhouse gas budgets, but can rapidly release large volumes of gas to the atmosphere. To quantify a robust annual ebullition flux we measured rates continuously for a year (2013-2014) using custom-built chambers deployed in a restored emergent wetland located in the Sacramento-San Joaquin Delta, CA. We combined ebullition flux rates with observations of gas concentrations to estimate annual ebullition emissions of CO2, CH4, and N2O and compare flux rates to whole-ecosystem exchange of CO2 and CH4 measured simultaneously by eddy covariance.Mean ebullition flux rates were 18.3 ± 5.6 L m-2 yr-1. Ebullition CH4 concentrations were very high and ranged from 23-76 % with a mean of 47 ± 2.9 %; CO2 concentrations were lower and ranged from 0.7-6.6 % with a mean of 2.8 ± 0.3 %; N2O concentrations were below atmospheric concentrations and ranged from 130-389 ppb(v) with a mean of 257 ± 13 ppb(v). We calculated well-constrained annual ebullition fluxes of: 6.2 ± 1.9 g CH4 m-2 yr-1, 1.0 ± 0.3 g CO2 m-2 yr-1 and 9.3 ± 2.8 mg N2O m-2 yr-1. Methane emissions via ebullition were very large, representing 15-25 % of total wetland CH4 emissions measured at this site, whereas ebullition released only relatively small quantities of CO2 and N2O. Our results demonstrate that large releases of CH4 via ebullition from open water surfaces can be a significant component of restored wetland greenhouse gas budgets.

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.

40 CFR 86.1809-01 - Prohibition of defeat devices.

Code of Federal Regulations, 2012 CFR

2012-07-01

... PROGRAMS (CONTINUED) CONTROL OF EMISSIONS FROM NEW AND IN-USE HIGHWAY VEHICLES AND ENGINES (CONTINUED) General Compliance Provisions for Control of Air Pollution From New and In-Use Light-Duty Vehicles, Light... emission control, the Administrator will use a guideline to determine the appropriateness of the CO...

40 CFR 86.1809-12 - Prohibition of defeat devices.

Code of Federal Regulations, 2010 CFR

2010-07-01

... PROGRAMS (CONTINUED) CONTROL OF EMISSIONS FROM NEW AND IN-USE HIGHWAY VEHICLES AND ENGINES (CONTINUED) General Compliance Provisions for Control of Air Pollution From New and In-Use Light-Duty Vehicles, Light... device. (c) For cold temperature CO and cold temperature NMHC emission control, the Administrator will...

40 CFR 86.1809-10 - Prohibition of defeat devices.

Code of Federal Regulations, 2010 CFR

2010-07-01

... PROGRAMS (CONTINUED) CONTROL OF EMISSIONS FROM NEW AND IN-USE HIGHWAY VEHICLES AND ENGINES (CONTINUED) General Compliance Provisions for Control of Air Pollution From New and In-Use Light-Duty Vehicles, Light... device. (c) For cold temperature CO and cold temperature NMHC emission control, the Administrator will...

40 CFR 86.1809-01 - Prohibition of defeat devices.

Code of Federal Regulations, 2010 CFR

2010-07-01

... PROGRAMS (CONTINUED) CONTROL OF EMISSIONS FROM NEW AND IN-USE HIGHWAY VEHICLES AND ENGINES (CONTINUED) General Compliance Provisions for Control of Air Pollution From New and In-Use Light-Duty Vehicles, Light... emission control, the Administrator will use a guideline to determine the appropriateness of the CO...

40 CFR 86.1809-01 - Prohibition of defeat devices.

Code of Federal Regulations, 2013 CFR

2013-07-01

... PROGRAMS (CONTINUED) CONTROL OF EMISSIONS FROM NEW AND IN-USE HIGHWAY VEHICLES AND ENGINES (CONTINUED) General Compliance Provisions for Control of Air Pollution From New and In-Use Light-Duty Vehicles, Light... emission control, the Administrator will use a guideline to determine the appropriateness of the CO...

40 CFR 86.1809-12 - Prohibition of defeat devices.

Code of Federal Regulations, 2013 CFR

2013-07-01

... PROGRAMS (CONTINUED) CONTROL OF EMISSIONS FROM NEW AND IN-USE HIGHWAY VEHICLES AND ENGINES (CONTINUED) General Compliance Provisions for Control of Air Pollution From New and In-Use Light-Duty Vehicles, Light... device. (c) For cold temperature CO and cold temperature NMHC emission control, the Administrator will...

40 CFR 86.1809-10 - Prohibition of defeat devices.

Code of Federal Regulations, 2011 CFR

2011-07-01

... PROGRAMS (CONTINUED) CONTROL OF EMISSIONS FROM NEW AND IN-USE HIGHWAY VEHICLES AND ENGINES (CONTINUED) General Compliance Provisions for Control of Air Pollution From New and In-Use Light-Duty Vehicles, Light... device. (c) For cold temperature CO and cold temperature NMHC emission control, the Administrator will...

40 CFR 86.1809-10 - Prohibition of defeat devices.

Code of Federal Regulations, 2013 CFR

2013-07-01

... PROGRAMS (CONTINUED) CONTROL OF EMISSIONS FROM NEW AND IN-USE HIGHWAY VEHICLES AND ENGINES (CONTINUED) General Compliance Provisions for Control of Air Pollution From New and In-Use Light-Duty Vehicles, Light... device. (c) For cold temperature CO and cold temperature NMHC emission control, the Administrator will...

40 CFR 86.1809-01 - Prohibition of defeat devices.

Code of Federal Regulations, 2011 CFR

2011-07-01

... PROGRAMS (CONTINUED) CONTROL OF EMISSIONS FROM NEW AND IN-USE HIGHWAY VEHICLES AND ENGINES (CONTINUED) General Compliance Provisions for Control of Air Pollution From New and In-Use Light-Duty Vehicles, Light... emission control, the Administrator will use a guideline to determine the appropriateness of the CO...

40 CFR 86.1809-12 - Prohibition of defeat devices.

Code of Federal Regulations, 2011 CFR

2011-07-01

... PROGRAMS (CONTINUED) CONTROL OF EMISSIONS FROM NEW AND IN-USE HIGHWAY VEHICLES AND ENGINES (CONTINUED) General Compliance Provisions for Control of Air Pollution From New and In-Use Light-Duty Vehicles, Light... device. (c) For cold temperature CO and cold temperature NMHC emission control, the Administrator will...

40 CFR 98.36 - Data reporting requirements.

Code of Federal Regulations, 2010 CFR

2010-07-01

... fossil fuels only, the annual CO2 emissions for all fuels combined. Reporting CO2 emissions by type of fuel is not required. (ii) For units that burn both fossil fuels and biomass, the annual CO2 emissions from combustion of all fossil fuels combined and the annual CO2 emissions from combustion of all...

[Diurnal changes in greenhouse gases at water-air interface of Xiangxi River in autumn and their influencing factors].

PubMed

Huang, Wen-Min; Zhu, Kong-Xian; Zhao, Wei; Yu, Bo-Shi; Yuan, Xi-Gong; Feng, Rui-Jie; Bi, Yong-Hong; Hu, Zheng-Yu

2013-04-01

With the closed chamber and gas chromatography method, a 24-hour continuous monitoring was carried out to understand the greenhouse gases fluxes across the water-air interface of the Xiangxi River Bay, the Three-Gorges Reservoir in Autumn. Results indicated that the fluxes of CO2, CH4 and N2O across the water-air interface showed an obvious diurnal variation. The absorption and emission process of CH4 showed strong diurnal variation during the experimental period, reaching the highest emission at 1 am, whereas CO2 and N2O were emitted all day. The fluxes of CO2 ranged from 20.1-97.5 mg x (m2 x h)(-1) at day and 32.7-42.5 mg x (m2 x h)(-1) at night, the fluxes of N2O ranged from 18.4-133.7 microg x (m2 x h)(-1) at day and 42.1-102.6 microg x (m2 x h)(-1) at night. The fluxes of CO2 had positive correlation with wind speed and negative correlation with pH. The fluxes of N2O had positive correlation with pH.

40 CFR 98.272 - GHGs to report.

Code of Federal Regulations, 2012 CFR

2012-07-01

... listed in paragraphs (a) through (f) of this section: (a) CO2, biogenic CO2, CH4, and N2O emissions from each kraft or soda chemical recovery furnace. (b) CO2, biogenic CO2, CH4, and N2O emissions from each sulfite chemical recovery combustion unit. (c) CO2, biogenic CO2, CH4, and N2O emissions from each stand...

40 CFR 98.272 - GHGs to report.

Code of Federal Regulations, 2010 CFR

2010-07-01

... listed in paragraphs (a) through (f) of this section: (a) CO2, biogenic CO2, CH4, and N2O emissions from each kraft or soda chemical recovery furnace. (b) CO2, biogenic CO2, CH4, and N2O emissions from each sulfite chemical recovery combustion unit. (c) CO2, biogenic CO2, CH4, and N2O emissions from each stand...

40 CFR 98.272 - GHGs to report.

Code of Federal Regulations, 2014 CFR

2014-07-01

... listed in paragraphs (a) through (f) of this section: (a) CO2, biogenic CO2, CH4, and N2O emissions from each kraft or soda chemical recovery furnace. (b) CO2, biogenic CO2, CH4, and N2O emissions from each sulfite chemical recovery combustion unit. (c) CO2, biogenic CO2, CH4, and N2O emissions from each stand...

40 CFR 98.272 - GHGs to report.

Code of Federal Regulations, 2013 CFR

2013-07-01

... listed in paragraphs (a) through (f) of this section: (a) CO2, biogenic CO2, CH4, and N2O emissions from each kraft or soda chemical recovery furnace. (b) CO2, biogenic CO2, CH4, and N2O emissions from each sulfite chemical recovery combustion unit. (c) CO2, biogenic CO2, CH4, and N2O emissions from each stand...

40 CFR 98.272 - GHGs to report.

Code of Federal Regulations, 2011 CFR

2011-07-01

... listed in paragraphs (a) through (f) of this section: (a) CO2, biogenic CO2, CH4, and N2O emissions from each kraft or soda chemical recovery furnace. (b) CO2, biogenic CO2, CH4, and N2O emissions from each sulfite chemical recovery combustion unit. (c) CO2, biogenic CO2, CH4, and N2O emissions from each stand...

Changes in the carbon footprint of Japanese households in an aging society.

PubMed

Shigetomi, Yosuke; Nansai, Keisuke; Kagawa, Shigemi; Tohno, Susumu

2014-06-03

As the aging and low birthrate trends continue in Japan, and as changes in the working population and consumption patterns occur, new factors are expected to have an impact on consumption-based greenhouse gas (GHG) emissions. We present the impacts of changes in the composition of Japanese households on GHG emission structures using current (2005) consumption-based accounting on the commodity sectors that are expected to require priority efforts for reducing emissions in 2035. This is done using the Global Link Input-Output model (GLIO) and domestic household consumption data and assuming that recent detailed consumption expenditures based on the Social Accounting Matrix (SAM) will continue into the future. The results show that consumption-based GHG emissions derived from Japanese household consumption in 2035 are estimated to be 1061 Mt-CO2eq (4.2% lower than in 2005). This study can be used to reveal more information and as a resource in developing policies to more meticulously and efficiently reduce emissions based on emission and import rates for each domestic and overseas commodity supply chain.

Measurement of CO 2, CO, SO 2, and NO emissions from coal-based thermal power plants in India

NASA Astrophysics Data System (ADS)

Chakraborty, N.; Mukherjee, I.; Santra, A. K.; Chowdhury, S.; Chakraborty, S.; Bhattacharya, S.; Mitra, A. P.; Sharma, C.

Measurements of CO 2 (direct GHG) and CO, SO 2, NO (indirect GHGs) were conducted on-line at some of the coal-based thermal power plants in India. The objective of the study was three-fold: to quantify the measured emissions in terms of emission coefficient per kg of coal and per kWh of electricity, to calculate the total possible emission from Indian thermal power plants, and subsequently to compare them with some previous studies. Instrument IMR 2800P Flue Gas Analyzer was used on-line to measure the emission rates of CO 2, CO, SO 2, and NO at 11 numbers of generating units of different ratings. Certain quality assurance (QA) and quality control (QC) techniques were also adopted to gather the data so as to avoid any ambiguity in subsequent data interpretation. For the betterment of data interpretation, the requisite statistical parameters (standard deviation and arithmetic mean) for the measured emissions have been also calculated. The emission coefficients determined for CO 2, CO, SO 2, and NO have been compared with their corresponding values as obtained in the studies conducted by other groups. The total emissions of CO 2, CO, SO 2, and NO calculated on the basis of the emission coefficients for the year 2003-2004 have been found to be 465.667, 1.583, 4.058, and 1.129 Tg, respectively.

Long-term changes in CO(2) emissions in Austria and Czechoslovakia-Identifying the drivers of environmental pressures.

PubMed

Gingrich, Simone; Kušková, Petra; Steinberger, Julia K

2011-02-01

This study presents fossil-fuel related CO(2) emissions in Austria and Czechoslovakia (current Czech Republic and Slovakia) for 1830-2000. The drivers of CO(2) emissions are discussed by investigating the variables of the standard Kaya identity for 1920-2000 and conducting a comparative Index Decomposition Analysis. Proxy data on industrial production and household consumption are analysed to understand the role of the economic structure. CO(2) emissions increased in both countries in the long run. Czechoslovakia was a stronger emitter of CO(2) throughout the time period, but per-capita emissions significantly differed only after World War I, when Czechoslovakia and Austria became independent. The difference in CO(2) emissions increased until the mid-1980s (the period of communism in Czechoslovakia), explained by the energy intensity and the composition effects, and higher industrial production in Czechoslovakia. Counterbalancing factors were the income effect and household consumption. After the Velvet revolution in 1990, Czechoslovak CO(2) emissions decreased, and the energy composition effect (and industrial production) lost importance. Despite their different political and economic development, Austria and Czechoslovakia reached similar levels of per-capita CO(2) emissions in the late 20th century. Neither Austrian "eco-efficiency" nor Czechoslovak restructuring have been effective in reducing CO(2) emissions to a sustainable level.

Sourcing methane and carbon dioxide emissions from a small city: Influence of natural gas leakage and combustion.

PubMed

Chamberlain, Samuel D; Ingraffea, Anthony R; Sparks, Jed P

2016-11-01

Natural gas leakage and combustion are major sources of methane (CH 4 ) and carbon dioxide (CO 2 ), respectively; however, our understanding of emissions from cities is limited. We mapped distribution pipeline leakage using a mobile CH 4 detection system, and continuously monitored atmospheric CO 2 and CH 4 concentrations and carbon isotopes (δ 13 C-CO 2 and δ 13 C-CH 4 ) for one-year above Ithaca, New York. Pipeline leakage rates were low (<0.39 leaks mile -1 ), likely due to the small extent of cast iron and bare steel within the distribution pipeline system (2.6%). Our atmospheric monitoring demonstrated that the isotopic composition of locally emitted CO 2 approached the δ 13 C range of natural gas combustion in winter, correlating to natural gas power generation patterns at Cornell's Combined Heat and Power Plant located 600 m southeast of the monitoring site. Atmospheric CH 4 plumes were primarily of natural gas origin, were observed intermittently throughout the year, and were most frequent in winter and spring. No correlations between the timing of atmospheric natural gas CH 4 plumes and Cornell Plant gas use patterns could be drawn. However, elevated CH 4 and CO 2 concentrations were observed coincident with high winds from the southeast, and the plant is the only major emission source in that wind sector. Our results demonstrate pipeline leakage rates are low in cities with a low extent of leak prone pipe, and natural gas power facilities may be an important source of urban and suburban emissions. Copyright © 2016 Elsevier Ltd. All rights reserved.

How light, temperature, and measurement and growth [CO2] interactively control isoprene emission in hybrid aspen

PubMed Central

Niinemets, Ülo; Sun, Zhihong

2015-01-01

Plant isoprene emissions have been modelled assuming independent controls by light, temperature and atmospheric [CO2]. However, the isoprene emission rate is ultimately controlled by the pool size of its immediate substrate, dimethylallyl diphosphate (DMADP), and isoprene synthase activity, implying that the environmental controls might interact. In addition, acclimation to growth [CO2] can shift the share of the control by DMADP pool size and isoprene synthase activity, and thereby alter the environmental sensitivity. Environmental controls of isoprene emission were studied in hybrid aspen (Populus tremula × Populus tremuloides) saplings acclimated either to ambient [CO2] of 380 μmol mol–1 or elevated [CO2] of 780 μmol mol–1. The data demonstrated strong interactive effects of environmental drivers and growth [CO2] on isoprene emissions. Light enhancement of isoprene emission was the greatest at intermediate temperatures and was greater in elevated-[CO2]-grown plants, indicating greater enhancement of the DMADP supply. The optimum temperature for isoprene emission was higher at lower light, suggesting activation of alternative DMADP sinks at higher light. In addition, [CO2] inhibition of isoprene emission was lost at a higher temperature with particularly strong effects in elevated-[CO2]-grown plants. Nevertheless, DMADP pool size was still predicted to more strongly control isoprene emission at higher temperatures in elevated-[CO2]-grown plants. We argue that interactive environmental controls and acclimation to growth [CO2] should be incorporated in future isoprene emission models at the level of DMADP pool size. PMID:25399006

Impact of elevated CO2, water table, and temperature changes on CO2 and CH4 fluxes from arctic tundra soils

NASA Astrophysics Data System (ADS)

Zona, Donatella; Haynes, Katherine; Deutschman, Douglas; Bryant, Emma; McEwing, Katherine; Davidson, Scott; Oechel, Walter

2015-04-01

Large uncertainties still exist on the response of tundra C emissions to future climate due, in part, to the lack of understanding of the interactive effects of potentially controlling variables on C emissions from Arctic ecosystems. In this study we subjected 48 soil cores (without active vegetation) from dominant arctic wetland vegetation types, to a laboratory manipulation of elevated atmospheric CO2, elevated temperature, and altered water table, representing current and future conditions in the Arctic for two growing seasons. To our knowledge this experiment comprised the most extensively replicated manipulation of intact soil cores in the Arctic. The hydrological status of the soil was the most dominant control on both soil CO2 and CH4 emissions. Despite higher soil CO2 emission occurring in the drier plots, substantial CO2 respiration occurred under flooded conditions, suggesting significant anaerobic respirations in these arctic tundra ecosystems. Importantly, a critical control on soil CO2 and CH4 fluxes was the original vascular plant cover. The dissolved organic carbon (DOC) concentration was correlated with cumulative CH4 emissions but not with cumulative CO2 suggesting C quality influenced CH4 production but not soil CO2 emissions. An interactive effect between increased temperature and elevated CO2 on soil CO2 emissions suggested a potential shift of the soils microbial community towards more efficient soil organic matter degraders with warming and elevated CO2. Methane emissions did not decrease over the course of the experiment, even with no input from vegetation. This result indicated that CH4 emissions are not carbon limited in these C rich soils. Overall CH4 emissions represented about 49% of the sum of total C (C-CO2 + C-CH4) emission in the wet treatments, and 15% in the dry treatments, representing a dominant component of the overall C balance from arctic soils.

Non-CO2 Greenhouse Gases: International Emissions and Projections

EPA Pesticide Factsheets

EPA August 2011 report on global non-CO2 emissions projections (1990-2030) for emissions of non-CO2 greenhouse gases (methane, nitrous oxide, and fluorinated greenhouse gases) from more than twenty emissions sources.

CO(2), CO, and Hg emissions from the Truman Shepherd and Ruth Mullins coal fires, eastern Kentucky, USA.

PubMed

O'Keefe, Jennifer M K; Henke, Kevin R; Hower, James C; Engle, Mark A; Stracher, Glenn B; Stucker, J D; Drew, Jordan W; Staggs, Wayne D; Murray, Tiffany M; Hammond, Maxwell L; Adkins, Kenneth D; Mullins, Bailey J; Lemley, Edward W

2010-03-01

Carbon dioxide (CO(2)), carbon monoxide (CO), and mercury (Hg) emissions were quantified for two eastern Kentucky coal-seam fires, the Truman Shepherd fire in Floyd County and the Ruth Mullins fire in Perry County. This study is one of the first to estimate gas emissions from coal fires using field measurements at gas vents. The Truman Shepherd fire emissions are nearly 1400t CO(2)/yr and 16kg Hg/yr resulting from a coal combustion rate of 450-550t/yr. The sum of CO(2) emissions from seven vents at the Ruth Mullins fire is 726+/-72t/yr, suggesting that the fire is consuming about 250-280t coal/yr. Total Ruth Mullins fire CO and Hg emissions are estimated at 21+/-1.8t/yr and >840+/-170g/yr, respectively. The CO(2) emissions are environmentally significant, but low compared to coal-fired power plants; for example, 3.9x10(6)t CO(2)/yr for a 514-MW boiler in Kentucky. Using simple calculations, CO(2) and Hg emissions from coal-fires in the U.S. are estimated at 1.4x10(7)-2.9x10(8)t/yr and 0.58-11.5t/yr, respectively. This initial work indicates that coal fires may be an important source of CO(2), CO, Hg and other atmospheric constituents.

Spatiotemporal Characteristics, Determinants and Scenario Analysis of CO2 Emissions in China Using Provincial Panel Data.

PubMed

Wang, Shaojian; Fang, Chuanglin; Li, Guangdong

2015-01-01

This paper empirically investigated the spatiotemporal variations, influencing factors and future emission trends of China's CO2 emissions based on a provincial panel data set. A series of panel econometric models were used taking the period 1995-2011 into consideration. The results indicated that CO2 emissions in China increased over time, and were characterized by noticeable regional discrepancies; in addition, CO2 emissions also exhibited properties of spatial dependence and convergence. Factors such as population scale, economic level and urbanization level exerted a positive influence on CO2 emissions. Conversely, energy intensity was identified as having a negative influence on CO2 emissions. In addition, the significance of the relationship between CO2 emissions and the four variables varied across the provinces based on their scale of economic development. Scenario simulations further showed that the scenario of middle economic growth, middle population increase, low urbanization growth, and high technology improvement (here referred to as Scenario BTU), constitutes the best development model for China to realize the future sustainable development. Based on these empirical findings, we also provide a number of policy recommendations with respect to the future mitigation of CO2 emissions.

Spatiotemporal Characteristics, Determinants and Scenario Analysis of CO2 Emissions in China Using Provincial Panel Data

PubMed Central

Wang, Shaojian

2015-01-01

This paper empirically investigated the spatiotemporal variations, influencing factors and future emission trends of China’s CO2 emissions based on a provincial panel data set. A series of panel econometric models were used taking the period 1995–2011 into consideration. The results indicated that CO2 emissions in China increased over time, and were characterized by noticeable regional discrepancies; in addition, CO2 emissions also exhibited properties of spatial dependence and convergence. Factors such as population scale, economic level and urbanization level exerted a positive influence on CO2 emissions. Conversely, energy intensity was identified as having a negative influence on CO2 emissions. In addition, the significance of the relationship between CO2 emissions and the four variables varied across the provinces based on their scale of economic development. Scenario simulations further showed that the scenario of middle economic growth, middle population increase, low urbanization growth, and high technology improvement (here referred to as Scenario BTU), constitutes the best development model for China to realize the future sustainable development. Based on these empirical findings, we also provide a number of policy recommendations with respect to the future mitigation of CO2 emissions. PMID:26397373

Tecnical Note: Analysis of non-regulated vehicular emissions by extractive FTIR spectrometry: tests on a hybrid car in Mexico City

NASA Astrophysics Data System (ADS)

Reyes, F.; Grutter, M.; Jazcilevich, A.; González-Oropeza, R.

2006-11-01

A methodology to acquire valuable information on the chemical composition and evolution of vehicular emissions is presented. The analysis of the gases is performed by passing a constant flow of a sample gas from the tail-pipe into a 10 L multi-pass cell. The absorption spectra within the cell are obtained using an FTIR spectrometer at 0.5 cm-1 resolution along a 13.1 m optical path. Additionally, the total flow from the exhaust is continuously measured from a differential pressure sensor on a textit{Pitot} tube installed at the exit of the exhaust. This configuration aims to obtain a good speciation capability by coadding spectra during 30 s and reporting the emission (in g/km) of both criteria and non-regulated pollutants, such as CO2, CO, NO, SO2, NH3, HCHO and some NMHC, during predetermined driving cycles. The advantages and disadvantages of increasing the measurement frequency, as well as the effect of other parameters such as spectral resolution, cell volume and flow rate, are discussed. To test and evaluate the proposed technique, experiments were performed on a dynamometer running FTP-75 and typical driving cycles for the Mexico City Metropolitan Area (MCMA) on a Toyota Prius hybrid vehicle. This car is an example of recent marketed automotive technology dedicated to reduced emissions, increasing the need for sensitive detection techniques. This study shows the potential of the proposed technique to measure and report in real time the emissions of a large variety of pollutants, even from a super ultra-low emission vehicle (SULEV). The emissions of HC's, NOx, CO and CO2 obtained here were compared to experiments performed in other locations with the same model vehicle. The proposed technique provides a tool for future studies comparing in detail the emissions of vehicles using alternative fuels and emission control systems.

A gas chromatograph system for semi-continuous greenhouse gas measurements at Puy de Dôme station, Central France

NASA Astrophysics Data System (ADS)

Lopez, M.; Schmidt, M.; Ramonet, M.; Bonne, J.-L.; Colomb, A.; Kazan, V.; Laj, P.; Pichon, J.-M.

2015-03-01

Three years of greenhouse gases measurements, obtained using a gas chromatograph (GC) system located at the Puy de Dôme station at 1465 m a.s.l. in Central France are presented. The GC system was installed in 2010 at Puy de Dôme and was designed for automatic and accurate semi-continuous measurements of atmospheric carbon dioxide, methane, nitrous oxide and sulfur hexafluoride mole fractions. We present in detail the instrumental set up and the calibration strategy, which together allow the GC to reach repeatabilities of 0.1 μmol mol-1, 1.2, 0.3 nmol mol-1 and 0.06 pmol mol-1 for CO2, CH4, N2O and SF6, respectively. Comparisons of the atmospheric time series with those obtained using other instruments shown that the GC system meets the World Meteorological Organization recommendations. The analysis of the three-year atmospheric time series revealed how the planetary boundary layer height drives the mole fractions observed at a mountain site such as Puy de Dôme where air masses alternate between the planetary boundary layer and the free troposphere. Accurate long-lived greenhouse gases measurements collocated with 222Rn measurements as an atmospheric tracer, allowed us to determine the CO2, CH4 and N2O emissions in the catchment area of the station. The derived CO2 surface flux revealed a clear seasonal cycle with net uptake by plant assimilation in the spring and net emission caused by the biosphere and burning of fossil fuel during the remainder of the year. We calculated a mean annual CO2 flux of 1150 t(CO2) km-2. The derived CH4 and N2O emissions in the station catchment area were 5.6 t(CH4) km-2 yr-1 and 1.5 t(N2O) km-2 yr-1, respectively. Our derived annual CH4 flux is in agreement with the national French inventory, whereas our derived N2O flux is five times larger than the same inventory.

PAH and soot emissions from burning components of medical waste: examination/surgical gloves and cotton pads.

PubMed

Levendis, Y A; Atal, A; Carlson, J B; Quintana, M D

2001-01-01

This is a laboratory investigation on the emissions from batch combustion of representative infectious ("red bag") medical waste components, such as medical examination latex gloves and sterile cotton pads. Plastics and cloth account for the majority of the red bag wastes by mass and, certainly, by volume. An electrically heated, horizontal muffle furnace was used for batch combustion of small quantities of shredded fuels (0.5-1.5 g) at a gas temperature of approximately 1000 degrees C. The residence time of the post-combustion gases in the furnace was approximately 1 s. At the exit of the furnace, the following emissions were measured: CO, CO2, NOx, particulates and polynuclear aromatic compounds (PACs). The first three gaseous emissions were measured with continuous gas analyzers. Soot and PAC emissions were simultaneously measured by passing the furnace effluent through a filter (to collect condensed-phase PACs) and a bed of XAD-4 adsorbent (to capture gaseous-phase PACs). Analysis involved soxhlet extraction, followed by gas chromatography-mass spectrometry (GC-MS). Results were contrasted with previously measured emissions from batch combustion of pulverized coal and tire-derived fuel (TDF) under similar conditions. Results showed that the particulate soot) and cumulative PAC emissions from batch combustion of latex gloves were more than an order of magnitude higher than those from cotton pads. The following values are indicative of the relative trends (but not necessarily absolute values) in emission yields: 26% of the mass of the latex was converted to soot, 11% of which was condensed PAC. Only 2% of the mass of cotton pads was converted to soot, and only 3% of the weight of that soot was condensed PAC. The PAC yields from latex were comparable to those from TDF. The PAC yields from cotton were higher than those from coal. A notable exception to this trend was that the three-ring gas-phase PAC yields from cotton were more significant than those from latex. Emission yields of CO and CO2 from batch combustion of cotton were, respectively, comparable and higher than those from latex, despite the fact that the carbon content of cotton was half that of latex. This is indicative of the more effective combustion of cotton. Nearly all of the mass of carbon of cotton gasified to CO and CO2 while only small fractions of the carbon in latex were converted to CO2 and CO (20% and 10%, respectively). Yields of NOx from batch combustions of latex and cotton accounted for 15% and 12%, respectively, of the mass of fuel nitrogen indicating that more fuel nitrogen was converted to NOx in the former case, possibly due to higher flame temperatures. No SO2 emissions were detected, indicating that during the fuel-rich combustion of latex, its sulfur content was converted to other compounds (such as H2S) or remained in the soot.

Monitoring gas and heat emissions at Norris Geyser Basin, Yellowstone National Park, USA based on a combined eddy covariance and Multi-GAS approach

USGS Publications Warehouse

Lewicki, Jennifer L.; Kelly, Peter; Bergfeld, Deborah; Vaughan, R. Greg; Lowenstern, Jacob B.

2017-01-01

We quantified gas and heat emissions in an acid-sulfate, vapor-dominated area (0.04-km2) of Norris Geyser Basin, located just north of the 0.63 Ma Yellowstone Caldera and near an area of anomalous uplift. From 14 May to 3 October 2016, an eddy covariance system measured half-hourly CO2, H2O and sensible (H) and latent (LE) heat fluxes and a Multi-GAS instrument measured (1 Hz frequency) atmospheric H2O, CO2 and H2S volumetric mixing ratios. We also measured soil CO2 fluxes using the accumulation chamber method and temperature profiles on a grid and collected fumarole gas samples for geochemical analysis. Eddy covariance CO2 fluxes ranged from − 56 to 885 g m− 2 d− 1. Using wavelet analysis, average daily eddy covariance CO2 fluxes were locally correlated with average daily environmental parameters on several-day to monthly time scales. Estimates of CO2emission rate from the study area ranged from 8.6 t d− 1 based on eddy covariance measurements to 9.8 t d− 1 based on accumulation chamber measurements. Eddy covariance water vapor fluxes ranged from 1178 to 24,600 g m− 2 d− 1. Nighttime H and LEwere considered representative of hydrothermal heat fluxes and ranged from 4 to 183 and 38 to 504 W m− 2, respectively. The total hydrothermal heat emission rate (H + LE + radiant) estimated for the study area was 11.6 MW and LE contributed 69% of the output. The mean ± standard deviation of H2O, CO2 and H2S mixing ratios measured by the Multi-GAS system were 9.3 ± 3.1 parts per thousand, 467 ± 61 ppmv, and 0.5 ± 0.6 ppmv, respectively, and variations in the gas compositions were strongly correlated with diurnal variations in environmental parameters (wind speed and direction, atmospheric temperature). After removing ambient H2O and CO2, the observed variations in the Multi-GAS data could be explained by the mixing of relatively H2O-CO2-H2S-rich fumarole gases with CO2-rich and H2O-H2S-poor soil gases. The fumarole H2O/CO2 and CO2/H2S end member ratios (101.7 and 27.1, respectively, on average) were invariant during the measurement period and fell within the range of values measured in direct fumarole gas samples. The soil gas H2O/CO2end member ratios (~ 15–30) were variable and low relative to the fumarole end member, likely resulting from water vapor loss during cooling and condensation in the shallow subsurface, whereas the CO2/H2S end member ratio was high (~ 160), presumably related to transport of CO2-dominated soil gas emissions mixed with trace fumarolic emissions to the Multi-GAS station. Nighttime eddy covariance ratios of H2O to CO2 flux were typically between the soil gas and fumarole end member H2O/CO2 ratios defined by Multi-GAS measurements. Overall, the combined eddy covariance and Multi-GAS approach provides a powerful tool for quasi-continuous measurements of gas and heat emissions for improved volcano-hydrothermal monitoring.

The engineering options for mitigating the climate impacts of aviation.

PubMed

Williams, Victoria

2007-12-15

Aviation is a growing contributor to climate change, with unique impacts due to the altitude of emissions. If existing traffic growth rates continue, radical engineering solutions will be required to prevent aviation becoming one of the dominant contributors to climate change. This paper reviews the engineering options for mitigating the climate impacts of aviation using aircraft and airspace technologies. These options include not only improvements in fuel efficiency, which would reduce carbon dioxide (CO2) emissions, but also measures to reduce non-CO2 impacts including the formation of persistent contrails. Integrated solutions to optimize environmental performance will require changes to airframes, engines, avionics, air traffic control systems and airspace design. While market-based measures, such as offset schemes and emissions trading, receive growing attention, this paper sets out the crucial role of engineering in the challenge to develop a 'green air traffic system'.

Advantages of a city-scale emission inventory for urban air quality research and policy: the case of Nanjing, a typical industrial city in the Yangtze River Delta, China

NASA Astrophysics Data System (ADS)

Zhao, Y.; Qiu, L. P.; Xu, R. Y.; Xie, F. J.; Zhang, Q.; Yu, Y. Y.; Nielsen, C. P.; Qin, H. X.; Wang, H. K.; Wu, X. C.; Li, W. Q.; Zhang, J.

2015-11-01

With most eastern Chinese cities facing major air quality challenges, there is a strong need for city-scale emission inventories for use in both chemical transport modeling and the development of pollution control policies. In this paper, a high-resolution emission inventory (with a horizontal resolution of 3 × 3 km) of air pollutants and CO2 for Nanjing, a typical large city in the Yangtze River Delta, is developed, incorporating the best available information on local sources. Emission factors and activity data at the unit or facility level are collected and compiled using a thorough on-site survey of major sources. Over 900 individual plants, which account for 97 % of the city's total coal consumption, are identified as point sources, and all of the emission-related parameters including combustion technology, fuel quality, and removal efficiency of air pollution control devices (APCD) are analyzed. New data-collection approaches including continuous emission monitoring systems and real-time monitoring of traffic flows are employed to improve spatiotemporal distribution of emissions. Despite fast growth of energy consumption between 2010 and 2012, relatively small interannual changes in emissions are found for most air pollutants during this period, attributed mainly to benefits of growing APCD deployment and the comparatively strong and improving regulatory oversight of the large point sources that dominate the levels and spatial distributions of Nanjing emissions overall. The improvement of this city-level emission inventory is indicated by comparisons with observations and other inventories at larger spatial scale. Relatively good spatial correlations are found for SO2, NOx, and CO between the city-scale emission estimates and concentrations at nine state-operated monitoring sites (R = 0.58, 0.46, and 0.61, respectively). The emission ratios of specific pollutants including BC to CO, OC to EC, and CO2 to CO compare well to top-down constraints from ground observations. The interannual variability and spatial distribution of NOx emissions are consistent with NO2 vertical column density measured by the Ozone Monitoring Instrument (OMI). In particular, the Nanjing city-scale emission inventory correlates better with satellite observations than the downscaled Multi-resolution Emission Inventory for China (MEIC) does when emissions from power plants are excluded. This indicates improvement in emission estimation for sectors other than power generation, notably industry and transportation. A high-resolution emission inventory may also provide a basis to consider the quality of instrumental observations. To further improve emission estimation and evaluation, more measurements of both emission factors and ambient levels of given pollutants are suggested; the uncertainties of emission inventories at city scale should also be fully quantified and compared with those at national scale.

Advantages of city-scale emission inventory for urban air quality research and policy: the case of Nanjing, a typical industrial city in the Yangtze River Delta, China

NASA Astrophysics Data System (ADS)

Zhao, Y.; Qiu, L.; Xu, R.; Xie, F.; Zhang, Q.; Yu, Y.; Nielsen, C. P.; Qin, H.; Wang, H.; Wu, X.; Li, W.; Zhang, J.

2015-07-01

With most eastern Chinese cities facing major air quality challenges, there is a strong need for city-scale emission inventories for use in both chemical transport modeling and the development of pollution control policies. In this paper, a high-resolution emission inventory of air pollutants and CO2 for Nanjing, a typical large city in the Yangtze River Delta, is developed incorporating the best available information on local sources. Emission factors and activity data at the unit or facility level are collected and compiled using a thorough onsite survey of major sources. Over 900 individual plants, which account for 97 % of the city's total coal consumption, are identified as point sources, and all of the emission-related parameters including combustion technology, fuel quality, and removal efficiency of air pollution control devices (APCD) are analyzed. New data-collection approaches including continuous emission monitoring systems and real-time monitoring of traffic flows are employed to improve spatiotemporal distribution of emissions. Despite fast growth of energy consumption between 2010 and 2012, relatively small inter-annual changes in emissions are found for most air pollutants during this period, attributed mainly to benefits of growing APCD deployment and the comparatively strong and improving regulatory oversight of the large point sources that dominate the levels and spatial distributions of Nanjing emissions overall. The improvement of this city-level emission inventory is indicated by comparisons with observations and other inventories at larger spatial scale. Relatively good spatial correlations are found for SO2, NOx, and CO between the city-scale emission estimates and concentrations at 9 state-opertated monitoring sites (R = 0.58, 0.46, and 0.61, respectively). The emission ratios of specific pollutants including BC to CO, OC to EC, and CO2 to CO compare well to top-down constraints from ground observations. The inter-annual variability and spatial distribution of NOx emissions are consistent with NO2 vertical column density measured by the Ozone Monitoring Instrument (OMI). In particular, the Nanjing city-scale emission inventory correlates better with satellite observations than the downscaled Multi-resolution Emission Inventory for China (MEIC) does when emissions from power plants are excluded. This indicates improvement in emission estimation for sectors other than power generation, notably industry and transportation. High-resolution emission inventory may also provide a basis to consider the quality of instrumental observations. To further improve emission estimation and evaluation, more measurements of both emission factors and ambient levels of given pollutants are suggested; the uncertainties of emission inventories at city scale should also be fully quantified and compared with those at national scale.

Winter crop CO2 uptake inferred from CONTRAIL CO2 measurements over Delhi, India

NASA Astrophysics Data System (ADS)

Umezawa, T.; Niwa, Y.; Sawa, Y.; Machida, T.; Matsueda, H.

2016-12-01

CONTRAIL is an ongoing project that measures atmospheric trace gases onboard aircraft of Japan Airlines. Atmospheric CO2 concentration is analyzed using Continuous CO2 Measuring Equipment (CME) during intercontinental flights. Since 2005, we have obtained >7 millions of data points of CO2 concentration along level-flight and ascent/descent tracks of >12 thousands flights with extensive coverage of the Asia-Pacific region. In this study, we analyze 787 vertical profiles of CO2 over Delhi, India. The surrounding area is mainly covered by irrigated croplands with patchy urban areas. We observed a general increase of CO2 toward the ground in the boundary layer throughout December-April due to urban CO2 emissions from the Delhi metropolitan area. In January-March, however, we frequently observed sharp decreases of CO2 below 2 km, indicating the existence of local CO2 sinks in this season. We calculated enhancement/depletion of CO2 amount in the boundary layer, and found clear depletion in February-March, coincident with the growing season of the winter crops (mainly wheat) in the region. It is also inferred that the crop uptake may exceed in magnitude the urban anthropogenic emissions from the Delhi area, indicating significance of agricultural CO2 fluxes in the regional carbon budget. Due to the winter crop uptake, CO2 concentration over Delhi shows no increasing/decreasing temporal trends during January-March when that at baseline stations at similar latitudes in the northern hemisphere increases steadily. This suggests that the CONTRAIL measurements capture local to regional flux signals that are not well resolved by the existing observation network.

A black alder plantation improves the greenhouse gas balance of a degraded moist peat grassland

NASA Astrophysics Data System (ADS)

Bereswill, Sarah; Hoffmann, Mathias; Huth, Vytas; Popova, Yulia; Zak, Dominik; Augustin, Jürgen

2017-04-01

Drained peatlands are among the strongest terrestrial sources of the greenhouse gases (GHG) CO2 and N2O. Therefore, activities of peatland revitalisation through rewetting, often combined with the implementation of peat forming vegetation, aim to restore the GHG sink function that is characteristic for pristine peatlands. Black alder (Alnus glutinosa) naturally occurs in temperate marshes and minerotrophic peatlands (= fens) and is also suitable for paludiculture, the cultivation of biomass on wet or rewetted peatlands. However, only little information exists, if a black alder plantation can reduce the climate impact of restored peatlands. Therefore, we investigated the effect of a newly established black alder plantation on the net GHG balance of a degraded fen in north-eastern Germany during a two-year study (August 2010 - August 2012). We compared the alder plantation (Awet) with an extensively used meadow (Mwet) both characterized by very moist soil conditions and a drier reference meadow (Mdry) characterized by moderately moist soil conditions. CO2, CH4 and N2O fluxes were measured monthly to bi-monthly with the manual closed chamber method. Fluxes were calculated using a modular R script and gap filled to obtain continuous daily fluxes. Awet was a net GHG sink of -4.8 t CO2-eq ha-1 yr-1, Mwet was climate neutral (-0.03 t CO2-eq ha-1 yr-1), and Mdry was a net GHG source of 15.7 t CO2-eq ha-1 yr-1. This was mainly caused by CO2 uptake at the two very moist sites and a high CO2 release at the drier reference site. In addition, Awet was a larger CO2 sink than Mwet, likely caused by an additional CO2 uptake of the alder stand. All sites were significant CH4 sources. Due to inundation following extraordinarily heavy precipitation in summer 2011 remarkable CH4emission peaks were found on all sites which accounted for up to 70 % of the cumulated two-year CH4emissions. However, overall Awet emitted significantly lesser CH4(4.9 g C m-2 yr-1). We assume that the black alders decreased the CH4emissions due to their effective O2 transport mechanism. N2O emissions were negligible at all three sites. Our results indicate that rewetting and planting black alders significantly improve the GHG balances of formerly drained fens already in the first two years after plantation. Furthermore, only one wet summer significantly increased the CH4 emissions of our study site, despite two-year average groundwater levels (GWL) of -0.2 to -0.35 m. This highlights the importance of acknowledging extreme precipitation events and groundwater fluctuations for the derivation of reliable GHG emission factors.

Hydrologic support of carbon dioxide flux revealed by whole-lake carbon budgets

USGS Publications Warehouse

Stets, E.G.; Striegl, Robert G.; Aiken, G.R.; Rosenberry, D.O.; Winter, T.C.

2009-01-01

Freshwater lakes are an important component of the global carbon cycle through both organic carbon (OC) sequestration and carbon dioxide (CO 2) emission. Most lakes have a net annual loss of CO2 to the atmosphere and substantial current evidence suggests that biologic mineralization of allochthonous OC maintains this flux. Because net CO 2 flux to the atmosphere implies net mineralization of OC within the lake ecosystem, it is also commonly assumed that net annual CO2 emission indicates negative net ecosystem production (NEP). We explored the relationship between atmospheric CO2 emission and NEP in two lakes known to have contrasting hydrologie characteristics and net CO2 emission. We calculated NEP for calendar year 2004 using whole-lake OC and inorganic carbon (IC) budgets, NEPoc and NEPIC, respectively, and compared the resulting values to measured annual CO 2 flux from the lakes. In both lakes, NEPIc and NEP Ic were positive, indicating net autotrophy. Therefore CO2 emission from these lakes was apparently not supported by mineralization of allochthonous organic material. In both lakes, hydrologie CO2 inputs, as well as CO2 evolved from netcalcite precipitation, could account for the net CO2 emission. NEP calculated from diel CO2 measurements was also affected by hydrologie inputs of CO2. These results indicate that CO2 emission and positive NEP may coincide in lakes, especially in carbonate terrain, and that all potential geologic, biogeochemical, and hydrologie sources of CO2 need to be accounted for when using CO2 concentrations to infer lake NEP. Copyright 2009 by the American Geophysical Union.

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.

CO 2 utilization and storage in shale gas reservoirs: Experimental results and economic impacts

DOE PAGES

Schaef, Herbert T.; Davidson, Casie L.; Owen, Antionette Toni; ...

2014-12-31

Natural gas is considered a cleaner and lower-emission fuel than coal, and its high abundance from advanced drilling techniques has positioned natural gas as a major alternative energy source for the U.S. However, each ton of CO 2 emitted from any type of fossil fuel combustion will continue to increase global atmospheric concentrations. One unique approach to reducing anthropogenic CO 2 emissions involves coupling CO 2 based enhanced gas recovery (EGR) operations in depleted shale gas reservoirs with long-term CO 2 storage operations. In this paper, we report unique findings about the interactions between important shale minerals and sorbing gasesmore » (CH 4 and CO 2) and associated economic consequences. Where enhanced condensation of CO 2 followed by desorption on clay surface is observed under supercritical conditions, a linear sorption profile emerges for CH 4. Volumetric changes to montmorillonites occur during exposure to CO 2. Theory-based simulations identify interactions with interlayer cations as energetically favorable for CO 2 intercalation. Thus, experimental evidence suggests CH 4 does not occupy the interlayer and has only the propensity for surface adsorption. Mixed CH 4:CO 2 gas systems, where CH 4 concentrations prevail, indicate preferential CO 2 sorption as determined by in situ infrared spectroscopy and X-ray diffraction techniques. Collectively, these laboratory studies combined with a cost-based economic analysis provide a basis for identifying favorable CO 2-EOR opportunities in previously fractured shale gas reservoirs approaching final stages of primary gas production. Moreover, utilization of site-specific laboratory measurements in reservoir simulators provides insight into optimum injection strategies for maximizing CH 4/CO 2 exchange rates to obtain peak natural gas production.« less

Assessing the Greenhouse Gas Emissions from Natural Gas Fired Power Plants

NASA Astrophysics Data System (ADS)

Hajny, K. D.; Shepson, P. B.; Rudek, J.; Stirm, B. H.; Kaeser, R.; Stuff, A. A.

2017-12-01

Natural gas is often discussed as a "bridge fuel" to transition to renewable energy as it only produces 51% the amount of CO2 per unit energy as coal. This, coupled with rapid increases in production fueled by technological advances, has led to a near tripling of natural gas used for electricity generation since 2005. One concern with this idea of a "bridge fuel" is that methane, the primary component of natural gas, is itself a potent greenhouse gas with 28 and 84 times the global warming potential of CO2 based on mass over a 100 and 20 year period, respectively. Studies have estimated that leaks from the point of extraction to end use of 3.2% would offset the climate benefits of natural gas. Previous work from our group saw that 3 combined cycle power plants emitted unburned CH4 from the stacks and leaked additional CH4 from equipment on site, but total loss rates were still less than 2.2%. Using Purdue's Airborne Laboratory for Atmospheric Research (ALAR) we completed additional aircraft based mass balance experiments combined with passes directly over power plant stacks to expand on the previous study. In this work, we have measured at 12 additional natural gas fired power plants including a mix of operation types (baseload, peaking, intermediate) and firing methods (combined cycle, simple thermal, combustion turbine). We have also returned to the 3 plants previously sampled to reinvestigate emissions for each of those, to assess reproducibility of the results. Here we report the comparison of reported continuous emissions monitoring systems (CEMS) data for CO2 to our emission rates calculated from mass balance experiments, as well as a comparison of calculated CH4 emission rates to estimated emission rates based on the EPA emission factor of 1 g CH4/mmbtu natural gas and CEMS reported heat input. We will also discuss emissions from a coal-fired plant which has been sampled by the group in the past and has since converted to natural gas. Lastly, we discuss the ratio of CH4 to CO2 in stack based emissions as it relates to our calculated emission rates and as compared to the same ratio for the emission factors.

Quantifying CO2 Emissions From Individual Power Plants From Space

NASA Astrophysics Data System (ADS)

Nassar, Ray; Hill, Timothy G.; McLinden, Chris A.; Wunch, Debra; Jones, Dylan B. A.; Crisp, David

2017-10-01

In order to better manage anthropogenic CO2 emissions, improved methods of quantifying emissions are needed at all spatial scales from the national level down to the facility level. Although the Orbiting Carbon Observatory 2 (OCO-2) satellite was not designed for monitoring power plant emissions, we show that in some cases, CO2 observations from OCO-2 can be used to quantify daily CO2 emissions from individual middle- to large-sized coal power plants by fitting the data to plume model simulations. Emission estimates for U.S. power plants are within 1-17% of reported daily emission values, enabling application of the approach to international sites that lack detailed emission information. This affirms that a constellation of future CO2 imaging satellites, optimized for point sources, could monitor emissions from individual power plants to support the implementation of climate policies.

Quantification of fossil fuel CO2 emissions at the urban scale: Results from the Indianapolis Flux Project (INFLUX)

NASA Astrophysics Data System (ADS)

Turnbull, J. C.; Cambaliza, M. L.; Sweeney, C.; Karion, A.; Newberger, T.; Tans, P. P.; Lehman, S.; Davis, K. J.; Miles, N. L.; Richardson, S.; Lauvaux, T.; Shepson, P.; Gurney, K. R.; Song, Y.; Razlivanov, I. N.

2012-12-01

Emissions of fossil fuel CO2 (CO2ff) from anthropogenic sources are the primary driver of observed increases in the atmospheric CO2 burden, and hence global warming. Quantification of the magnitude of fossil fuel CO2 emissions is vital to improving our understanding of the global and regional carbon cycle, and independent evaluation of reported emissions is essential to the success of any emission reduction efforts. The urban scale is of particular interest, because ~75% CO2ff is emitted from urban regions, and cities are leading the way in attempts to reduce emissions. Measurements of 14CO2 can be used to determine CO2ff, yet existing 14C measurement techniques require laborious laboratory analysis and measurements are often insufficient for inferring an urban emission flux. This presentation will focus on how 14CO2 measurements can be combined with those of more easily measured ancillary tracers to obtain high resolution CO2ff mixing ratio estimates and then infer the emission flux. A pilot study over Sacramento, California showed strong correlations between CO2ff and carbon monoxide (CO) and demonstrated an ability to quantify the urban flux, albeit with large uncertainties. The Indianapolis Flux Project (INFLUX) aims to develop and assess methods to quantify urban greenhouse gas emissions. Indianapolis was chosen as an ideal test case because it has relatively straightforward meteorology; a contained, isolated, urban region; and substantial and well-known fossil fuel CO2 emissions. INFLUX incorporates atmospheric measurements of a suite of gases and isotopes including 14C from light aircraft and from a network of existing tall towers surrounding the Indianapolis urban area. The recently added CO2ff content is calculated from measurements of 14C in CO2, and then convolved with atmospheric transport models and ancillary data to estimate the urban CO2ff emission flux. Significant innovations in sample collection include: collection of hourly averaged samples to remove short term atmospheric variability; and direct measurement of the background signal from towers immediately upwind of the urban area and from the boundary layer. We find that CO2ff and other anthropogenic trace gases are consistently enhanced at a tower site downwind of the city. Measurements made directly over or very close to the urban area show only weak correlations between CO2ff and trace gases associated with combustion, likely because the urban plume is not yet well mixed. Total CO2 is also consistently enhanced in the downwind samples, even in summer. In winter, total CO2 enhancement is slightly higher than the fossil fuel CO2 enhancement, in agreement with Indiana's requirement for 10% bioethanol use in gasoline. This result implies that the enhancement in total CO2 can be used to infer CO2ff emissions for Indianapolis during winter. We therefore use the high resolution in situ total CO2 measurements in a simple mass balance model to estimate the urban CO2ff emissions. An initial comparison shows a ~20% difference between the top-down and bottom-up methods.

Multiscale observations of CO2, 13CO2, and pollutants at Four Corners for emission verification and attribution

PubMed Central

Lindenmaier, Rodica; Dubey, Manvendra K.; Henderson, Bradley G.; Butterfield, Zachary T.; Herman, Jay R.; Rahn, Thom; Lee, Sang-Hyun

2014-01-01

There is a pressing need to verify air pollutant and greenhouse gas emissions from anthropogenic fossil energy sources to enforce current and future regulations. We demonstrate the feasibility of using simultaneous remote sensing observations of column abundances of CO2, CO, and NO2 to inform and verify emission inventories. We report, to our knowledge, the first ever simultaneous column enhancements in CO2 (3–10 ppm) and NO2 (1–3 Dobson Units), and evidence of δ13CO2 depletion in an urban region with two large coal-fired power plants with distinct scrubbing technologies that have resulted in ∆NOx/∆CO2 emission ratios that differ by a factor of two. Ground-based total atmospheric column trace gas abundances change synchronously and correlate well with simultaneous in situ point measurements during plume interceptions. Emission ratios of ∆NOx/∆CO2 and ∆SO2/∆CO2 derived from in situ atmospheric observations agree with those reported by in-stack monitors. Forward simulations using in-stack emissions agree with remote column CO2 and NO2 plume observations after fine scale adjustments. Both observed and simulated column ∆NO2/∆CO2 ratios indicate that a large fraction (70–75%) of the region is polluted. We demonstrate that the column emission ratios of ∆NO2/∆CO2 can resolve changes from day-to-day variation in sources with distinct emission factors (clean and dirty power plants, urban, and fires). We apportion these sources by using NO2, SO2, and CO as signatures. Our high-frequency remote sensing observations of CO2 and coemitted pollutants offer promise for the verification of power plant emission factors and abatement technologies from ground and space. PMID:24843169

Quantitative Estimation of the Climatic Effects of Carbon Transferred by International Trade.

PubMed

Wei, Ting; Dong, Wenjie; Moore, John; Yan, Qing; Song, Yi; Yang, Zhiyong; Yuan, Wenping; Chou, Jieming; Cui, Xuefeng; Yan, Xiaodong; Wei, Zhigang; Guo, Yan; Yang, Shili; Tian, Di; Lin, Pengfei; Yang, Song; Wen, Zhiping; Lin, Hui; Chen, Min; Feng, Guolin; Jiang, Yundi; Zhu, Xian; Chen, Juan; Wei, Xin; Shi, Wen; Zhang, Zhiguo; Dong, Juan; Li, Yexin; Chen, Deliang

2016-06-22

Carbon transfer via international trade affects the spatial pattern of global carbon emissions by redistributing emissions related to production of goods and services. It has potential impacts on attribution of the responsibility of various countries for climate change and formulation of carbon-reduction policies. However, the effect of carbon transfer on climate change has not been quantified. Here, we present a quantitative estimate of climatic impacts of carbon transfer based on a simple CO2 Impulse Response Function and three Earth System Models. The results suggest that carbon transfer leads to a migration of CO2 by 0.1-3.9 ppm or 3-9% of the rise in the global atmospheric concentrations from developed countries to developing countries during 1990-2005 and potentially reduces the effectiveness of the Kyoto Protocol by up to 5.3%. However, the induced atmospheric CO2 concentration and climate changes (e.g., in temperature, ocean heat content, and sea-ice) are very small and lie within observed interannual variability. Given continuous growth of transferred carbon emissions and their proportion in global total carbon emissions, the climatic effect of traded carbon is likely to become more significant in the future, highlighting the need to consider carbon transfer in future climate negotiations.

Non-CO2 greenhouse gases and climate change.

PubMed

Montzka, S A; Dlugokencky, E J; Butler, J H

2011-08-03

Earth's climate is warming as a result of anthropogenic emissions of greenhouse gases, particularly carbon dioxide (CO(2)) from fossil fuel combustion. Anthropogenic emissions of non-CO(2) greenhouse gases, such as methane, nitrous oxide and ozone-depleting substances (largely from sources other than fossil fuels), also contribute significantly to warming. Some non-CO(2) greenhouse gases have much shorter lifetimes than CO(2), so reducing their emissions offers an additional opportunity to lessen future climate change. Although it is clear that sustainably reducing the warming influence of greenhouse gases will be possible only with substantial cuts in emissions of CO(2), reducing non-CO(2) greenhouse gas emissions would be a relatively quick way of contributing to this goal.

Explaining CO2 fluctuations observed in snowpacks

NASA Astrophysics Data System (ADS)

Graham, Laura; Risk, David

2018-02-01

Winter soil carbon dioxide (CO2) respiration is a significant and understudied component of the global carbon (C) cycle. Winter soil CO2 fluxes can be surprisingly variable, owing to physical factors such as snowpack properties and wind. This study aimed to quantify the effects of advective transport of CO2 in soil-snow systems on the subdiurnal to diurnal (hours to days) timescale, use an enhanced diffusion model to replicate the effects of CO2 concentration depletions from persistent winds, and use a model-measure pairing to effectively explore what is happening in the field. We took continuous measurements of CO2 concentration gradients and meteorological data at a site in the Cape Breton Highlands of Nova Scotia, Canada, to determine the relationship between wind speeds and CO2 levels in snowpacks. We adapted a soil CO2 diffusion model for the soil-snow system and simulated stepwise changes in transport rate over a broad range of plausible synthetic cases. The goal was to mimic the changes we observed in CO2 snowpack concentration to help elucidate the mechanisms (diffusion, advection) responsible for observed variations. On subdiurnal to diurnal timescales with varying winds and constant snow levels, a strong negative relationship between wind speed and CO2 concentration within the snowpack was often identified. Modelling clearly demonstrated that diffusion alone was unable to replicate the high-frequency CO2 fluctuations, but simulations using above-atmospheric snowpack diffusivities (simulating advective transport within the snowpack) reproduced snow CO2 changes of the observed magnitude and speed. This confirmed that wind-induced ventilation contributed to episodic pulsed emissions from the snow surface and to suppressed snowpack concentrations. This study improves our understanding of winter CO2 dynamics to aid in continued quantification of the annual global C cycle and demonstrates a preference for continuous wintertime CO2 flux measurement systems.

A {sup 13}CO Detection in a Brightest Cluster Galaxy

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

Vantyghem, A. N.; McNamara, B. R.; Hogan, M. T.

We present ALMA Cycle 4 observations of CO(1-0), CO(3-2), and {sup 13}CO(3-2) line emission in the brightest cluster galaxy (BCG) of RXJ0821+0752. This is one of the first detections of {sup 13}CO line emission in a galaxy cluster. Half of the CO(3-2) line emission originates from two clumps of molecular gas that are spatially offset from the galactic center. These clumps are surrounded by diffuse emission that extends 8 kpc in length. The detected {sup 13}CO emission is confined entirely to the two bright clumps, with any emission outside of this region lying below our detection threshold. Two distinct velocitymore » components with similar integrated fluxes are detected in the {sup 12}CO spectra. The narrower component (60 km s{sup −1} FWHM) is consistent in both velocity centroid and linewidth with {sup 13}CO(3-2) emission, while the broader (130–160 km s{sup −1}), slightly blueshifted wing has no associated {sup 13}CO(3-2) emission. A simple local thermodynamic model indicates that the {sup 13}CO emission traces 2.1 × 10{sup 9} M {sub ⊙} of molecular gas. Isolating the {sup 12}CO velocity component that accompanies the {sup 13}CO emission yields a CO-to-H{sub 2} conversion factor of α {sub CO} = 2.3 M {sub ⊙} (K km s{sup −1}){sup −1}, which is a factor of two lower than the Galactic value. Adopting the Galactic CO-to-H{sub 2} conversion factor in BCGs may therefore overestimate their molecular gas masses by a factor of two. This is within the object-to-object scatter from extragalactic sources, so calibrations in a larger sample of clusters are necessary in order to confirm a sub-Galactic conversion factor.« less

CO2 emissions from German drinking water reservoirs.

PubMed

Saidi, Helmi; Koschorreck, Matthias

2017-03-01

Globally, reservoirs are a significant source of atmospheric CO 2 . However, precise quantification of greenhouse gas emissions from drinking water reservoirs on the regional or national scale is still challenging. We calculated CO 2 fluxes for 39 German drinking water reservoirs during a period of 22years (1991-2013) using routine monitoring data in order to quantify total emission of CO 2 from drinking water reservoirs in Germany and to identify major drivers. All reservoirs were a net CO 2 source with a median flux of 167gCm -2 y -1 , which makes gaseous emissions a relevant process for the carbon budget of each reservoir. Fluxes varied seasonally with median fluxes of 13, 48, and 201gCm -2 y -1 in spring, summer, and autumn respectively. Differences between reservoirs appeared to be primarily caused by the concentration of CO 2 in the surface water rather than by the physical gas transfer coefficient. Consideration of short term fluctuations of the gas transfer coefficient due to varying wind speed had only a minor effect on the annual budgets. High CO 2 emissions only occurred in reservoirs with pH<7 and total alkalinity <0.2mEql -1 . Annual CO 2 emissions correlated exponentially with pH but not with dissolved organic carbon (DOC). There was significant correlation between land use in the catchment and CO 2 emissions. In total, German drinking water reservoirs emit 44000t of CO 2 annually, which makes them a negligible CO 2 source (<0.005% of national CO 2 emissions) in Germany. Copyright © 2017 Elsevier B.V. All rights reserved.

Seasonal and temporal CO2 dynamics in three tropical mangrove creeks - A revision of global mangrove CO2 emissions

NASA Astrophysics Data System (ADS)

Rosentreter, Judith A.; Maher, D. T.; Erler, D. V.; Murray, R.; Eyre, B. D.

2018-02-01

Continuous high-resolution surface water pCO2 and δ13C-CO2 and 222Rn (dry season only) were measured over two tidal cycles in the wet and dry season in three tropical tidal mangrove creeks on the north-eastern coast of Queensland, Australia. Mangrove surface water pCO2 followed a clear tidal pattern (ranging from 387 to 13,031 μatm) with higher pCO2-values in the wet season than in the dry season. The δ13C-CO2 in the mangrove waters ranged from -21.7 to -8.8‰ and was rather indicative of a mixed source than a distinct mangrove signature. Surface water CO2 was likely driven by a combination of mangrove and external carbon sources, e.g. exchange with groundwater/pore water enriched in 13C, or terrestrial carbon inputs with a significant contribution of C4-vegetation (sugar cane) source. The kinetic and equilibrium fractionation during the gas exchange at the water-atmosphere interface may have further caused a 13C-enrichment of the CO2 pool in the mangrove surface waters. Average CO2 evasion rates (58.7-277.6 mmol m-2 d-1) were calculated using different empirical gas transfer velocity models. Using our high-resolution time series data and previously published data, the average CO2 flux rate in mangrove ecosystems was estimated to be 56.5 ± 8.9 mmol m-2 d-1, which corresponds to a revised global mangrove CO2 emission of 34.1 ± 5.4 Tg C per year.

Assessment of the Contribution of Poultry and Pig Production to Greenhouse Gas Emissions in South Korea Over the Last 10 Years (2005 through 2014).

PubMed

Boontiam, Waewaree; Shin, Yongjin; Choi, Hong Lim; Kumari, Priyanka

2016-12-01

The goal of this study was to estimate the emissions of greenhouse gases (GHG), namely methane (CH 4 ), nitrous oxide (N 2 O), and carbon dioxide (CO 2 ) from poultry and pig production in South Korea over the last 10 years (2005 through 2014). The calculations of GHG emissions were based on Intergovernmental Panel on Climate Change (IPCC) guidelines. Over the study period, the CH 4 emission from manure management decreased in layer chickens, nursery to finishing pigs and gestating to lactating sows, but there was a gradual increase in CH 4 emission from broiler chickens and male breeding pigs. Both sows and nursery to finishing pigs were associated with greater emissions from enteric fermentation than the boars, especially in 2009. Layer chickens produced lower direct and indirect N 2 O emissions from 2009 to 2014, whereas the average direct and indirect N 2 O emissions from manure management for broiler chickens were 12.48 and 4.93 Gg CO 2 -eq/yr, respectively. Annual direct and indirect N 2 O emissions for broiler chickens tended to decrease in 2014. Average CO 2 emission from direct on-farm energy uses for broiler and layer chickens were 46.62 and 136.56 Gg CO 2 -eq/yr, respectively. For pig sectors, the N 2 O emission from direct and indirect sources gradually increased, but they decreased for breeding pigs. Carbon dioxide emission from direct on-farm energy uses reached a maximum of 53.93 Gg CO 2 -eq/yr in 2009, but this total gradually declined in 2010 and 2011. For boars, the greatest CO 2 emission occurred in 2012 and was 9.44 Gg CO 2 -eq/yr. Indirect N 2 O emission was the largest component of GHG emissions in broilers. In layer chickens, the largest contributing factor to GHG emissions was CO 2 from direct on-farm energy uses. For pig production, the largest component of GHG emissions was CH 4 from manure management, followed by CO 2 emission from direct on-farm energy use and CH 4 enteric fermentation emission, which accounted for 8.47, 2.85, and 2.82 Gg-CO 2 /yr, respectively. The greatest GHG emission intensity occurred in female breeding sows relative to boars. Overall, it is an important issue for the poultry and pig industry of South Korea to reduce GHG emissions with the effective approaches for the sustainability of agricultural practices.

Assessment of the Contribution of Poultry and Pig Production to Greenhouse Gas Emissions in South Korea Over the Last 10 Years (2005 through 2014)

PubMed Central

Boontiam, Waewaree; Shin, Yongjin; Choi, Hong Lim; Kumari, Priyanka

2016-01-01

The goal of this study was to estimate the emissions of greenhouse gases (GHG), namely methane (CH4), nitrous oxide (N2O), and carbon dioxide (CO2) from poultry and pig production in South Korea over the last 10 years (2005 through 2014). The calculations of GHG emissions were based on Intergovernmental Panel on Climate Change (IPCC) guidelines. Over the study period, the CH4 emission from manure management decreased in layer chickens, nursery to finishing pigs and gestating to lactating sows, but there was a gradual increase in CH4 emission from broiler chickens and male breeding pigs. Both sows and nursery to finishing pigs were associated with greater emissions from enteric fermentation than the boars, especially in 2009. Layer chickens produced lower direct and indirect N2O emissions from 2009 to 2014, whereas the average direct and indirect N2O emissions from manure management for broiler chickens were 12.48 and 4.93 Gg CO2-eq/yr, respectively. Annual direct and indirect N2O emissions for broiler chickens tended to decrease in 2014. Average CO2 emission from direct on-farm energy uses for broiler and layer chickens were 46.62 and 136.56 Gg CO2-eq/yr, respectively. For pig sectors, the N2O emission from direct and indirect sources gradually increased, but they decreased for breeding pigs. Carbon dioxide emission from direct on-farm energy uses reached a maximum of 53.93 Gg CO2-eq/yr in 2009, but this total gradually declined in 2010 and 2011. For boars, the greatest CO2 emission occurred in 2012 and was 9.44 Gg CO2-eq/yr. Indirect N2O emission was the largest component of GHG emissions in broilers. In layer chickens, the largest contributing factor to GHG emissions was CO2 from direct on-farm energy uses. For pig production, the largest component of GHG emissions was CH4 from manure management, followed by CO2 emission from direct on-farm energy use and CH4 enteric fermentation emission, which accounted for 8.47, 2.85, and 2.82 Gg-CO2/yr, respectively. The greatest GHG emission intensity occurred in female breeding sows relative to boars. Overall, it is an important issue for the poultry and pig industry of South Korea to reduce GHG emissions with the effective approaches for the sustainability of agricultural practices. PMID:26954125

Analysis of the impact path on factors of China's energy-related CO2 emissions: a path analysis with latent variables.

PubMed

Chen, Wenhui; Lei, Yalin

2017-02-01

Identifying the impact path on factors of CO 2 emissions is crucial for the government to take effective measures to reduce carbon emissions. The most existing research focuses on the total influence of factors on CO 2 emissions without differentiating between the direct and indirect influence. Moreover, scholars have addressed the relationships among energy consumption, economic growth, and CO 2 emissions rather than estimating all the causal relationships simultaneously. To fill this research gaps and explore overall driving factors' influence mechanism on CO 2 emissions, this paper utilizes a path analysis model with latent variables (PA-LV) to estimate the direct and indirect effect of factors on China's energy-related carbon emissions and to investigate the causal relationships among variables. Three key findings emanate from the analysis: (1) The change in the economic growth pattern inhibits the growth rate of CO 2 emissions by reducing the energy intensity; (2) adjustment of industrial structure contributes to energy conservation and CO 2 emission reduction by raising the proportion of the tertiary industry; and (3) the growth of CO 2 emissions impacts energy consumption and energy intensity negatively, which results in a negative impact indirectly on itself. To further control CO 2 emissions, the Chinese government should (1) adjust the industrial structure and actively develop its tertiary industry to improve energy efficiency and develop low-carbon economy, (2) optimize population shifts to avoid excessive population growth and reduce energy consumption, and (3) promote urbanization steadily to avoid high energy consumption and low energy efficiency.

Carbon dioxide, methane, and nitrous oxide emissions from a rice-wheat rotation as affected by crop residue incorporation and temperature

NASA Astrophysics Data System (ADS)

Zou, Jianwen; Huang, Yao; Zong, Lianggang; Zheng, Xunhua; Wang, Yuesi

2004-10-01

Field measurements were made from June 2001 to May 2002 to evaluate the effect of crop residue application and temperature on CO2, CH4, and N2O emissions within an entire rice-wheat rotation season. Rapeseed cake and wheat straw were incorporated into the soil at a rate of 2.25 t hm-2 when the rice crop was transplanted in June 2001. Compared with the control, the incorporation of rapeseed cake enhanced the emissions of CO2, CH4, and N2O in the rice-growing season by 12.3%, 252.3%, and 17.5%, respectively, while no further effect was held on the emissions of CO2 and N2O in the following wheatgrowing season. The incorporation of wheat straw enhanced the emissions of CO2 and CH4 by 7.1% and 249.6%, respectively, but reduced the N2O emission by 18.8% in the rice-growing season. Significant reductions of 17.8% for the CO2 and of 12.9% for the N2O emission were observed in the following wheatgrowing season. A positive correlation existed between the emissions of N2O and CO2 ( R 2 = 0.445, n = 73, p < 0.001) from the rice-growing season when N2O was emitted. A trade-off relationship between the emissions of CH4 and N2O was found in the rice-growing season. The CH4 emission was significantly correlated with the CO2 emission for the period from rice transplantation to field drainage, but not for the entire rice-growing season. In addition, air temperature was found to regulate the CO2 emissions from the non-waterlogged period over the entire rice-wheat rotation season and the N2O emissions from the nonwaterlogged period of the rice-growing season, which can be quantitatively described by an exponential function. The temperature coefficient ( Q 10) was then evaluated to be 2.3±0.2 for the CO2 emission and 3.9±0.4 for the N2O emission, respectively.

Energy consumption and CO2 emissions in Tibet and its cities in 2014

NASA Astrophysics Data System (ADS)

Shan, Yuli; Zheng, Heran; Guan, Dabo; Li, Chongmao; Mi, Zhifu; Meng, Jing; Schroeder, Heike; Ma, Jibo; Ma, Zhuguo

2017-08-01

Because of its low level of energy consumption and the small scale of its industrial development, the Tibet Autonomous Region has historically been excluded from China's reported energy statistics, including those regarding CO2 emissions. In this paper, we estimate Tibet's energy consumption using limited online documents, and we calculate the 2014 energy-related and process-related CO2 emissions of Tibet and its seven prefecture-level administrative divisions for the first time. Our results show that 5.52 million tons of CO2 were emitted in Tibet in 2014; 33% of these emissions are associated with cement production. Tibet's emissions per capita amounted to 1.74 tons in 2014, which is substantially lower than the national average, although Tibet's emission intensity is relatively high at 0.60 tons per thousand yuan in 2014. Among Tibet's seven prefecture-level administrative divisions, Lhasa City and Shannan Region are the two largest CO2 contributors and have the highest per capita emissions and emission intensities. The Nagqu and Nyingchi regions emit little CO2 due to their farming/pasturing-dominated economies. This quantitative measure of Tibet's regional CO2 emissions provides solid data support for Tibet's actions on climate change and emission reductions.

Study of carbon dioxide emission inventory from transportation sector at Kualanamu International Airport

NASA Astrophysics Data System (ADS)

Suryati, I.; Indrawan, I.; Alihta, K. N.

2018-02-01

Transportation includes sources of greenhouse gas emission contributor in the form of carbon dioxide (CO2). CO2 is one of the air pollutant gases that cause climate change. The source of CO2 emissions at airports comes from road and air transportation. Kualanamu International Airport is one of the public service airports in North Sumatera Province. The purpose of this study is to inventory the emission loads generated by motor vehicles and aircraft and to forecast contributions of CO2 emissions from motor vehicles and aircraft. The research method used is quantitative and qualitative methods. The quantitative method used is to estimate emission loads of motor vehicles based on vehicle volume and emission factors derived from the literature and using the Tier-2 method to calculate the aircraft emission loads. The results for the maximum CO2 concentration were 6,206,789.37 μg/m3 and the minimal CO2 concentration was 4,070,674.84 μg/Nm3. The highest aircraft CO2 emission load is 200,164,424.5 kg/hr (1.75 x 109 ton/year) and the lowest is 38,884,064.5 kg/hr (3.40 x 108 ton/year). Meanwhile, the highest CO2 emission load from motor vehicles was 51,299.25 gr/hr (449,38 ton/year) and the lowest was 38,990.42 gr/hr (341,55 ton/year). CO2 contribution from a motor vehicle is 65% and 5% from aircraft in Kualanamu International Airport.

40 CFR 86.127-00 - Test procedures; overview.

Code of Federal Regulations, 2013 CFR

2013-07-01

... following emissions: (1) Gaseous exhaust THC, CO, NOX. CO2 (for petroleum-fueled and gaseous- fueled... vehicles). (b) The FTP Otto-cycle exhaust emission test is designed to determine gaseous THC, CO, CO2, CH4... determine gaseous THC, NMHC, CO, CO2, CH4, and NOX emissions from gasoline-fueled or diesel-fueled vehicles...

40 CFR 86.127-00 - Test procedures; overview.

Code of Federal Regulations, 2014 CFR

2014-07-01

... following emissions: (1) Gaseous exhaust THC, CO, NOX. CO2 (for petroleum-fueled and gaseous- fueled... vehicles). (b) The FTP Otto-cycle exhaust emission test is designed to determine gaseous THC, CO, CO2, CH4... determine gaseous THC, NMHC, CO, CO2, CH4, and NOX emissions from gasoline-fueled or diesel-fueled vehicles...

40 CFR 86.127-00 - Test procedures; overview.

Code of Federal Regulations, 2012 CFR

2012-07-01

... following emissions: (1) Gaseous exhaust THC, CO, NOX. CO2 (for petroleum-fueled and gaseous- fueled... vehicles). (b) The FTP Otto-cycle exhaust emission test is designed to determine gaseous THC, CO, CO2, CH4... determine gaseous THC, NMHC, CO, CO2, CH4, and NOX emissions from gasoline-fueled or diesel-fueled vehicles...

How light, temperature, and measurement and growth [CO2] interactively control isoprene emission in hybrid aspen.

PubMed

Niinemets, Ülo; Sun, Zhihong

2015-02-01

Plant isoprene emissions have been modelled assuming independent controls by light, temperature and atmospheric [CO2]. However, the isoprene emission rate is ultimately controlled by the pool size of its immediate substrate, dimethylallyl diphosphate (DMADP), and isoprene synthase activity, implying that the environmental controls might interact. In addition, acclimation to growth [CO2] can shift the share of the control by DMADP pool size and isoprene synthase activity, and thereby alter the environmental sensitivity. Environmental controls of isoprene emission were studied in hybrid aspen (Populus tremula × Populus tremuloides) saplings acclimated either to ambient [CO2] of 380 μmol mol(-1) or elevated [CO2] of 780 μmol mol(-1). The data demonstrated strong interactive effects of environmental drivers and growth [CO2] on isoprene emissions. Light enhancement of isoprene emission was the greatest at intermediate temperatures and was greater in elevated-[CO2]-grown plants, indicating greater enhancement of the DMADP supply. The optimum temperature for isoprene emission was higher at lower light, suggesting activation of alternative DMADP sinks at higher light. In addition, [CO2] inhibition of isoprene emission was lost at a higher temperature with particularly strong effects in elevated-[CO2]-grown plants. Nevertheless, DMADP pool size was still predicted to more strongly control isoprene emission at higher temperatures in elevated-[CO2]-grown plants. We argue that interactive environmental controls and acclimation to growth [CO2] should be incorporated in future isoprene emission models at the level of DMADP pool size. © The Author 2014. Published by Oxford University Press on behalf of the Society for Experimental Biology.

Forest carbon stocks and fluxes in physiographic zones of India.

PubMed

Sheikh, Mehraj A; Kumar, Munesh; Bussman, Rainer W; Todaria, Np

2011-12-25

Reducing carbon Emissions from Deforestation and Degradation (REDD+) is of central importance to combat climate change. Foremost among the challenges is quantifying nation's carbon emissions from deforestation and degradation, which requires information on forest carbon storage. Here we estimated carbon storage in India's forest biomass for the years 2003, 2005 and 2007 and the net flux caused by deforestation and degradation, between two assessment periods i.e., Assessment Period first (ASP I), 2003-2005 and Assessment Period second (ASP II), 2005-2007. The total estimated carbon stock in India's forest biomass varied from 3325 to 3161 Mt during the years 2003 to 2007 respectively. There was a net flux of 372 Mt of CO2 in ASP I and 288 Mt of CO2 in ASP II, with an annual emission of 186 and 114 Mt of CO2 respectively. The carbon stock in India's forest biomass decreased continuously from 2003 onwards, despite slight increase in forest cover. The rate of carbon loss from the forest biomass in ASP II has dropped by 38.27% compared to ASP I. With the Copenhagen Accord, India along with other BASIC countries China, Brazil and South Africa is voluntarily going to cut emissions. India will voluntary reduce the emission intensity of its GDP by 20-25% by 2020 in comparison to 2005 level, activities like REDD+ can provide a relatively cost-effective way of offsetting emissions, either by increasing the removals of greenhouse gases from the atmosphere by afforestation programmes, managing forests, or by reducing emissions through deforestation and degradation.

Forest carbon stocks and fluxes in physiographic zones of India

PubMed Central

2011-01-01

Background Reducing carbon Emissions from Deforestation and Degradation (REDD+) is of central importance to combat climate change. Foremost among the challenges is quantifying nation's carbon emissions from deforestation and degradation, which requires information on forest carbon storage. Here we estimated carbon storage in India's forest biomass for the years 2003, 2005 and 2007 and the net flux caused by deforestation and degradation, between two assessment periods i.e., Assessment Period first (ASP I), 2003-2005 and Assessment Period second (ASP II), 2005-2007. Results The total estimated carbon stock in India's forest biomass varied from 3325 to 3161 Mt during the years 2003 to 2007 respectively. There was a net flux of 372 Mt of CO2 in ASP I and 288 Mt of CO2 in ASP II, with an annual emission of 186 and 114 Mt of CO2 respectively. The carbon stock in India's forest biomass decreased continuously from 2003 onwards, despite slight increase in forest cover. The rate of carbon loss from the forest biomass in ASP II has dropped by 38.27% compared to ASP I. Conclusion With the Copenhagen Accord, India along with other BASIC countries China, Brazil and South Africa is voluntarily going to cut emissions. India will voluntary reduce the emission intensity of its GDP by 20-25% by 2020 in comparison to 2005 level, activities like REDD+ can provide a relatively cost-effective way of offsetting emissions, either by increasing the removals of greenhouse gases from the atmosphere by afforestation programmes, managing forests, or by reducing emissions through deforestation and degradation. PMID:22196920

Estimated HCFC-22 emissions for 1990-2050 in China and the increasing contribution to global emissions

NASA Astrophysics Data System (ADS)

Li, Zhifang; Bie, Pengju; Wang, Ziyuan; Zhang, Zhaoyang; Jiang, Hanyu; Xu, Weiguang; Zhang, Jianbo; Hu, Jianxin

2016-05-01

Chlorodifluoromethane (CHClF2, HCFC-22) is a widely used refrigerant and foaming agent that is not only an ozone-depleting substance (ozone depletion potential (ODP), 0.04) but also a greenhouse gas (global warming potential (GWP), 1780). A comprehensive historical emission inventory for 1990-2014 was produced using a bottom-up method, and a projection through to 2050 was made for China. The results demonstrated that historical emissions increased sharply from 0.2 Gg/yr in 1990 to 127.2 Gg/yr in 2014. Room air-conditioners (RACs), industrial and commercial refrigeration (ICR), and extruded polystyrene (XPS) were three primary emission sources, and accounted for an average of 95.4% of the total emissions over the period studied. The percentage of global HCFC-22 emissions originating from China significantly increased from 0.1% in 1990 to 31.6% in 2012, with an average growth rate of 1.4% per year. Under the Montreal Protocol phasing-out (MPPO) scenario, future emissions were expected to reach a peak of 133.5 Gg/yr in 2016 and then continuously decline to 10.2 Gg/yr in 2050. The accumulative reduction for 2015-2050 would be 5533.8 Gg (equivalent to 221.4 CFC-11-eq Gg and 9850.1 CO2-eq Tg), which is approximately equivalent to the total CO2 emission for China in 2012 (9900 Tg) (Olivier et al., 2013), compared with the no Montreal Protocol scenario (NMP). Under the MPPO scenario, two cases were analyzed to explore the future emission ranges in China. A comparison between the two cases implied that the choice of emission reduction policy will have a considerable impact on HCFC-22 emissions.

Experimental multi-phase H2O-CO2 brine interactions at elevated temperature and pressure: Implications for CO2 sequestration in deep-saline aquifers

USGS Publications Warehouse

Rosenbauer, R.; Koksalan, T.

2004-01-01

The burning of fossil fuel and other anthropogenic activities have caused a continuous and dramatic 30% increase of atmospheric CO2 over the past 150 yr. CO2 sequestration is increasingly being viewed as a tool for managing these anthropogenic CO2 emissions to the atmosphere. CO2-saturated brine-rock experiments were carried out to evaluate the effects of multiphase H2O-CO2 fluids on mineral equilibria and the potential for CO2 sequestration in mineral phases within deep-saline aquifers. Experimental results were generally consistent with theoretical thermodynamic calculations. The solubility of CO2 was enhanced in brines in the presence of both limestone and sandstone relative to brines alone. Reactions between CO2 saturated brines and arkosic sandstones were characterized by desiccation of the brine and changes in the chemical composition of the brine suggesting fixation of CO2 in mineral phases. These reactions were occurring on a measurable but kinetically slow time scale at 120??C.

Growth in emission transfers via international trade from 1990 to 2008.

PubMed

Peters, Glen P; Minx, Jan C; Weber, Christopher L; Edenhofer, Ottmar

2011-05-24

Despite the emergence of regional climate policies, growth in global CO(2) emissions has remained strong. From 1990 to 2008 CO(2) emissions in developed countries (defined as countries with emission-reduction commitments in the Kyoto Protocol, Annex B) have stabilized, but emissions in developing countries (non-Annex B) have doubled. Some studies suggest that the stabilization of emissions in developed countries was partially because of growing imports from developing countries. To quantify the growth in emission transfers via international trade, we developed a trade-linked global database for CO(2) emissions covering 113 countries and 57 economic sectors from 1990 to 2008. We find that the emissions from the production of traded goods and services have increased from 4.3 Gt CO(2) in 1990 (20% of global emissions) to 7.8 Gt CO(2) in 2008 (26%). Most developed countries have increased their consumption-based emissions faster than their territorial emissions, and non-energy-intensive manufacturing had a key role in the emission transfers. The net emission transfers via international trade from developing to developed countries increased from 0.4 Gt CO(2) in 1990 to 1.6 Gt CO(2) in 2008, which exceeds the Kyoto Protocol emission reductions. Our results indicate that international trade is a significant factor in explaining the change in emissions in many countries, from both a production and consumption perspective. We suggest that countries monitor emission transfers via international trade, in addition to territorial emissions, to ensure progress toward stabilization of global greenhouse gas emissions.

Growth in emission transfers via international trade from 1990 to 2008

PubMed Central

Peters, Glen P.; Minx, Jan C.; Weber, Christopher L.; Edenhofer, Ottmar

2011-01-01

Despite the emergence of regional climate policies, growth in global CO2 emissions has remained strong. From 1990 to 2008 CO2 emissions in developed countries (defined as countries with emission-reduction commitments in the Kyoto Protocol, Annex B) have stabilized, but emissions in developing countries (non-Annex B) have doubled. Some studies suggest that the stabilization of emissions in developed countries was partially because of growing imports from developing countries. To quantify the growth in emission transfers via international trade, we developed a trade-linked global database for CO2 emissions covering 113 countries and 57 economic sectors from 1990 to 2008. We find that the emissions from the production of traded goods and services have increased from 4.3 Gt CO2 in 1990 (20% of global emissions) to 7.8 Gt CO2 in 2008 (26%). Most developed countries have increased their consumption-based emissions faster than their territorial emissions, and non–energy-intensive manufacturing had a key role in the emission transfers. The net emission transfers via international trade from developing to developed countries increased from 0.4 Gt CO2 in 1990 to 1.6 Gt CO2 in 2008, which exceeds the Kyoto Protocol emission reductions. Our results indicate that international trade is a significant factor in explaining the change in emissions in many countries, from both a production and consumption perspective. We suggest that countries monitor emission transfers via international trade, in addition to territorial emissions, to ensure progress toward stabilization of global greenhouse gas emissions. PMID:21518879

Biogeologic Carbon Sequestration - a Cost-Effective Proposal

NASA Astrophysics Data System (ADS)

Shaw, G. H.; Kuhns, R.

2009-05-01

Carbon sequestration has been proposed as a strategy for reducing the impact of carbon dioxide emissions from burning of fossil fuels. There are two main routes: 1) capture CO2 emissions from power plants or other large point sources followed by some form of "burial/sequestration", and 2) extraction of CO2 from the ambient atmosphere (involving substantial concentration relative to atmospheric levels) also followed by burial/sequestration. In either case the goal is to achieve significant long-term isolation of CO2 at an economically sustainable price, perhaps measured by some "market price" for CO2, such as the European carbon futures market, where the price is now (2/3/09) about 14-15/tonne of CO2. The second approach, removal of CO2 from the atmosphere, has the potential benefit of reversing the previous buildup of atmospheric CO2, and perhaps even providing a means to "adjust" terrestrial climate by regulating atmospheric CO2 concentrations. For the present, ideas of planetary "geo-engineering" are not as popular as reducing the impact of continued CO2 emissions. In fact, the energy and capital costs of extraction from a dilute atmosphere appear to make this approach uneconomical. Proposals to fertilize the open ocean suffer from concerns about long term ecosystem effects, to say nothing of a lack of verifiability. There is, however, an approach using biological systems that can not only extract significant amounts of CO2, but can do so cost-effectively. Lakes are known in which primary productivity approaches or exceeds 1gm C/cm2-yr. This equates to removal of 35,000 tonnes of CO2 per km2 per year, with a "market value" of about 500,000/yr. Such productivity only occurs under highly eutrophic conditions, and presumably requires significant nutrient additions. As such it would be unthinkable to pursue this technique on a large scale in extant lakes. If, however, it is possible to produce one or more large artificial lakes under acceptable conditions it is conceivable that this approach to carbon sequestration could prove invaluable in both the near and long term.

Secular Variations of Soil CO2 Efflux at Santa Ana-Izalco-Coatepeque Volcanic Complex, El Salvador, Central America

NASA Astrophysics Data System (ADS)

Olmos, R.; Barahona, F.; Cartagena, R.; Soriano, T.; Salazar, J.; Hernandez, P.; Perez, N.; Lopez, D.

2002-12-01

The Santa Ana-Izalco-Coatepeque volcanic complex (2,365 m elevation), located 40 Km west of San Salvador, consists of the Coatepeque collapse caldera (a 6.5 x 10.5 Km elliptical depression), the Santa Ana and Izalco stratovolcanoes, as well as numerous cinder cones and explosion craters. The summit of the Santa Ana volcano contains an acid lake where hot springs, gas bubbling and intense fumarolic emissions occur. A volcanic plume, usually driven by the NE trades, may be seen rising up to 500 m from the summit crater of the Santa Ana volcano. The goal of this study is to provide a multidisciplinary approach for the volcanic surveillance by means of performing geochemical continuous monitoring of diffuse CO2 emission rate in addition to seismic monitoring. Temporal variations of soil CO2 efflux measured at Cerro Pacho dome, Coatepeque caldera, by means of the accumulation chamber method and using a CO2 efflux continuous monitoring station developed by WEST Systems (Italy). From May 2001 till May 2002, CO2 efflux ranged from 4.3 to 327 gm-2d-1, with a median value of 98 and a quartile range of 26 gm-2d-1. Two distinct diffuse CO2 degassing periods have been observed: (1) an increasing trend from May to July 2001, and (2) a stationary period from November 2001 to May 2002. The increasing-trend period may be due to the anomalous plume degassing at the Santa Ana volcano during 2001 and soon after the January and February 2001 earthquakes. Temporal variations of CO2 efllux during the second period seem to be coupled with those of barometric pressure and wind speed at different time scales, though most of the variance is contained at diurnal and semi-diurnal frequencies. These observations can help to explain the existence of a persistent behavior (Hurst exponent, H=0.934 +/- 0.0039) within the diffuse CO2 degassing phenomena. However, further observations are in progress to understand the long-term memory of diffuse CO2 degassing at the Santa Ana volcanic complex.

40 CFR Table 6 to Subpart Zzzz of... - Continuous Compliance With Emission Limitations, and Other Requirements

Code of Federal Regulations, 2014 CFR

2014-07-01

... >500 HP located at a major source of HAP a. Reduce CO emissions and using an oxidation catalyst, and... not using an oxidation catalyst, and using a CPMS i. Conducting semiannual performance tests for CO to... RICE exhaust and using oxidation catalyst or NSCR i. Conducting semiannual performance tests for...

40 CFR Table 6 to Subpart Zzzz of... - Continuous Compliance With Emission Limitations, and Other Requirements

Code of Federal Regulations, 2013 CFR

2013-07-01

... >500 HP located at a major source of HAP a. Reduce CO emissions and using an oxidation catalyst, and... not using an oxidation catalyst, and using a CPMS i. Conducting semiannual performance tests for CO to... RICE exhaust and using oxidation catalyst or NSCR i. Conducting semiannual performance tests for...

Different sources of soil CO2 respiration from a drained spruce forest and their dependence on environmental factors

NASA Astrophysics Data System (ADS)

Nousratpour, A.

2011-12-01

The annual CO2 emission from soils corresponds to a large portion of the global carbon cycle and equals 10 percent of the total atmospheric carbon pool. The total forest soil CO2 loss equals the sum of contribution from autotrophic and heterotrophic organisms. The autotrophic respiration is derived from recent photosynthates from the forest canopy and exudates via the roots. The heterotrophic respiration is less directly dependent on root presence and recently assimilated photosynthates, which points to the possibility of separate mechanisms governing the CO2 emissions. The variation of the CO2 flux from these some-what overlapping sources in the soil i.e. rhizospheric and non-rhizosperically is still not fully understood. Soil temperature and water availability in particular have often been used to explain the variation of soil CO2 efflux by using regression methods. In this experiment around 1000 hours of soil CO2-emission rates from a drained spruce forest was collected from 6 plots, among which 3 were previously root excluded. The emission rates were collected during 5 campaigns throughout the growing season along with continuous above ground and below ground temperature and water properties such as precipitation and VPD (vapor pressure deficit). The resulting matrix was analyzed using multivariate statistical model PLSr (Partial Least Squares regression). This operation reduces the dimensionality of large datasets with probable multicollinearity and helps clarify the dependence of a response factor on x- variables. In addition a time series analysis is applied to the dataset to address the time lag between below ground temperature and water properties to the above ground weather conditions such as VPD and air temperature. Mean carbon emission from the control plots (428 mg Carbon m-2 hr-1) was significantly larger than that from the root excluded plots (136 mg Carbon m-2 hr-1). During the growing season more than 2/3 of the total CO2 release was estimated to be root contribution. The results show that the activity in the rhizosphere increased with rising soil temperature, VPD and ground water depletion until a certain point. When the level of ground water depth was deeper than about 0.5 m the dependence was reversed. This effect was either the opposite or lacking in the root excluded plots, which reflects the involvement of the tree roots and the separate factors controlling the different sources of CO2.

Long-term changes in CO2 emissions in Austria and Czechoslovakia—Identifying the drivers of environmental pressures

PubMed Central

Gingrich, Simone; Kušková, Petra; Steinberger, Julia K.

2011-01-01

This study presents fossil-fuel related CO2 emissions in Austria and Czechoslovakia (current Czech Republic and Slovakia) for 1830–2000. The drivers of CO2 emissions are discussed by investigating the variables of the standard Kaya identity for 1920–2000 and conducting a comparative Index Decomposition Analysis. Proxy data on industrial production and household consumption are analysed to understand the role of the economic structure. CO2 emissions increased in both countries in the long run. Czechoslovakia was a stronger emitter of CO2 throughout the time period, but per-capita emissions significantly differed only after World War I, when Czechoslovakia and Austria became independent. The difference in CO2 emissions increased until the mid-1980s (the period of communism in Czechoslovakia), explained by the energy intensity and the composition effects, and higher industrial production in Czechoslovakia. Counterbalancing factors were the income effect and household consumption. After the Velvet revolution in 1990, Czechoslovak CO2 emissions decreased, and the energy composition effect (and industrial production) lost importance. Despite their different political and economic development, Austria and Czechoslovakia reached similar levels of per-capita CO2 emissions in the late 20th century. Neither Austrian “eco-efficiency” nor Czechoslovak restructuring have been effective in reducing CO2 emissions to a sustainable level. PMID:21461052

Testing a high resolution CO2 and CO emission inventory against atmospheric observations in Salt Lake City, Utah for policy applications

NASA Astrophysics Data System (ADS)

Mendoza, D. L.; Lin, J. C.; Mitchell, L.; Gurney, K. R.; Patarasuk, R.; Mallia, D. V.; Fasoli, B.; Bares, R.; Catharine, D.; O'Keeffe, D.; Song, Y.; Huang, J.; Horel, J.; Crosman, E.; Hoch, S.; Ehleringer, J. R.

2016-12-01

We address the need for robust highly-resolved emissions and trace gas concentration data required for planning purposes and policy development aimed at managing pollutant sources. Adverse health effects resulting from urban pollution exposure are the result of proximity to emission sources and atmospheric mixing, necessitating models with high spatial and temporal resolution. As urban emission sources co-emit carbon dioxide (CO2) and criteria air pollutants (CAPs), efforts to reduce specific pollutants would synergistically reduce others. We present a contemporary (2010-2015) emissions inventory and modeled CO2 and carbon monoxide (CO) concentrations for Salt Lake County, Utah. We compare emissions transported by a dispersion model against stationary measurement data and present a systematic quantification of uncertainties. The emissions inventory for CO2 is based on the Hestia emissions data inventory that resolves emissions at hourly, building and road-link resolutions, as well as on an hourly gridded scale. The emissions were scaled using annual Energy Information Administration (EIA) fuel consumption data. We derived a CO emissions inventory using methods similar to Hestia, downscaling total county emissions from the 2011 Environmental Protection Agency's (EPA) National Emissions Inventory (NEI). The gridded CO emissions were compared against the Hestia CO2 gridded data to characterize spatial similarities and differences between them. Correlations were calculated at multiple scales of aggregation. The Stochastic Time-Inverted Lagrangian Trasport (STILT) dispersion model was used to transport emissions and estimate pollutant concentrations at an hourly resolution. Modeled results were compared against stationary measurements in the Salt Lake County area. This comparison highlights spatial locations and hours of high variability and uncertainty. Sensitivity to biological fluxes as well as to specific economic sectors was tested by varying their contributions to modeled concentrations and calibrating their emissions.

Emissions from prescribed burning of agricultural fields in the Pacific Northwest

NASA Astrophysics Data System (ADS)

Holder, A. L.; Gullett, B. K.; Urbanski, S. P.; Elleman, R.; O'Neill, S.; Tabor, D.; Mitchell, W.; Baker, K. R.

2017-10-01

Prescribed burns of winter wheat stubble and Kentucky bluegrass fields in northern Idaho and eastern Washington states (U.S.A.) were sampled using ground-, aerostat-, airplane-, and laboratory-based measurement platforms to determine emission factors, compare methods, and provide a current and comprehensive set of emissions data for air quality models, climate models, and emission inventories. Batch measurements of PM2.5, volatile organic compounds (VOCs), polycyclic aromatic hydrocarbons (PAHs), and polychlorinated dibenzodioxins/dibenzofurans (PCDDs/PCDFs), and continuous measurements of black carbon (BC), particle mass by size, CO, CO2, CH4, and aerosol characteristics were taken at ground level, on an aerostat-lofted instrument package, and from an airplane. Biomass samples gathered from the field were burned in a laboratory combustion facility for comparison with these ground and aerial field measurements. Emission factors for PM2.5, organic carbon (OC), CH4, and CO measured in the field study platforms were typically higher than those measured in the laboratory combustion facility. Field data for Kentucky bluegrass suggest that biomass residue loading is directly proportional to the PM2.5 emission factor; no such relationship was found with the limited wheat data. CO2 and BC emissions were higher in laboratory burn tests than in the field, reflecting greater carbon oxidation and flaming combustion conditions. These distinctions between field and laboratory results can be explained by measurements of the modified combustion efficiency (MCE). Higher MCEs were recorded in the laboratory burns than from the airplane platform. These MCE/emission factor trends are supported by 1-2 min grab samples from the ground and aerostat platforms. Emission factors measured here are similar to other studies measuring comparable fuels, pollutants, and combustion conditions. The size distribution of refractory BC (rBC) was single modal with a log-normal shape, which was consistent among fuel types when normalized by total rBC mass. The field and laboratory measurements of the Angstrom exponent (α) and single scattering albedo (ω) exhibit a strong decreasing trend with increasing MCEs in the range of 0.9-0.99. Field measurements of α and ω were consistently higher than laboratory burns, which is likely due to less complete combustion. When VOC emissions are compared with MCE, the results are consistent for both fuel types: emission factors increase as MCE decreases.

Multidecadal increase in North Atlantic coccolithophores and the potential role of rising CO2

NASA Astrophysics Data System (ADS)

Rivero-Calle, Sara; Gnanadesikan, Anand; Del Castillo, Carlos E.; Balch, William M.; Guikema, Seth D.

2015-12-01

As anthropogenic carbon dioxide (CO2) emissions acidify the oceans, calcifiers generally are expected to be negatively affected. However, using data from the Continuous Plankton Recorder, we show that coccolithophore occurrence in the North Atlantic increased from ~2 to more than 20% from 1965 through 2010. We used random forest models to examine more than 20 possible environmental drivers of this change, finding that CO2 and the Atlantic Multidecadal Oscillation were the best predictors, leading us to hypothesize that higher CO2 levels might be encouraging growth. A compilation of 41 independent laboratory studies supports our hypothesis. Our study shows a long-term basin-scale increase in coccolithophores and suggests that increasing CO2 and temperature have accelerated the growth of a phytoplankton group that is important for carbon cycling.

40 CFR 98.213 - Calculating GHG emissions.

Code of Federal Regulations, 2012 CFR

2012-07-01

... emissions. You must determine CO2 process emissions from carbonate use in accordance with the procedures specified in either paragraphs (a) or (b) of this section. (a) Calculate the process emissions of CO2 using calcination fractions with Equation U-1 of this section. ER30OC09.077 Where: ECO2 = Annual CO2 mass emissions...

40 CFR 98.213 - Calculating GHG emissions.

Code of Federal Regulations, 2013 CFR

2013-07-01

... emissions. You must determine CO2 process emissions from carbonate use in accordance with the procedures specified in either paragraphs (a) or (b) of this section. (a) Calculate the process emissions of CO2 using calcination fractions with Equation U-1 of this section. ER30OC09.077 Where: ECO2 = Annual CO2 mass emissions...

40 CFR 98.213 - Calculating GHG emissions.

Code of Federal Regulations, 2011 CFR

2011-07-01

... emissions. You must determine CO2 process emissions from carbonate use in accordance with the procedures specified in either paragraphs (a) or (b) of this section. (a) Calculate the process emissions of CO2 using calcination fractions with Equation U-1 of this section. ER30OC09.077 Where: ECO2 = Annual CO2 mass emissions...

40 CFR 98.213 - Calculating GHG emissions.

Code of Federal Regulations, 2014 CFR

2014-07-01

... emissions. You must determine CO2 process emissions from carbonate use in accordance with the procedures specified in either paragraphs (a) or (b) of this section. (a) Calculate the process emissions of CO2 using calcination fractions with Equation U-1 of this section. ER30OC09.077 Where: ECO2 = Annual CO2 mass emissions...

Methane and CO2 emissions from China's hydroelectric reservoirs: a new quantitative synthesis.

PubMed

Li, Siyue; Zhang, Quanfa; Bush, Richard T; Sullivan, Leigh A

2015-04-01

Controversy surrounds the green credentials of hydroelectricity because of the potentially large emission of greenhouse gases (GHG) from associated reservoirs. However, limited and patchy data particularly for China is constraining the current global assessment of GHG releases from hydroelectric reservoirs. This study provides the first evaluation of the CO2 and CH4 emissions from China's hydroelectric reservoirs by considering the reservoir water surface and drawdown areas, and downstream sources (including spillways and turbines, as well as river downstream). The total emission of 29.6 Tg CO2/year and 0.47 Tg CH4/year from hydroelectric reservoirs in China, expressed as CO2 equivalents (eq), corresponds to 45.6 Tg CO2eq/year, which is 2-fold higher than the current GHG emission (ca. 23 Tg CO2eq/year) from global temperate hydropower reservoirs. China's average emission of 70 g CO2eq/kWh from hydropower amounts to 7% of the emissions from coal-fired plant alternatives. China's hydroelectric reservoirs thus currently mitigate GHG emission when compared to the main alternative source of electricity with potentially far great reductions in GHG emissions and benefits possible through relatively minor changes to reservoir management and design. On average, the sum of drawdown and downstream emission including river reaches below dams and turbines, which is overlooked by most studies, represents the equivalent of 42% of the CO2 and 92% of CH4 that emit from hydroelectric reservoirs in China. Main drivers on GHG emission rates are summarized and highlight that water depth and stratification control CH4 flux, and CO2 flux shows significant negative relationships with pH, DO, and Chl-a. Based on our finding, a substantial revision of the global carbon emissions from hydroelectric reservoirs is warranted.

40 CFR 98.193 - Calculating GHG emissions.

Code of Federal Regulations, 2012 CFR

2012-07-01

... Stationary Fuel Combustion Sources). (2) Calculate and report process and combustion CO2 emissions separately... Stationary Fuel Combustion Sources) the combustion CO2 emissions from each lime kiln according to the... must calculate and report the annual process CO2 emissions from all lime kilns combined using the...

40 CFR 98.193 - Calculating GHG emissions.

Code of Federal Regulations, 2013 CFR

2013-07-01

... Stationary Fuel Combustion Sources). (2) Calculate and report process and combustion CO2 emissions separately... Stationary Fuel Combustion Sources) the combustion CO2 emissions from each lime kiln according to the... must calculate and report the annual process CO2 emissions from all lime kilns combined using the...

Reduction of CO2 Emissions Due to Wind Energy - Methods and Issues in Estimating Operational Emission Reductions

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

Holttinen, Hannele; Kiviluoma, Juha; McCann, John

2015-10-05

This paper presents ways of estimating CO2 reductions of wind power using different methodologies. Estimates based on historical data have more pitfalls in methodology than estimates based on dispatch simulations. Taking into account exchange of electricity with neighboring regions is challenging for all methods. Results for CO2 emission reductions are shown from several countries. Wind power will reduce emissions for about 0.3-0.4 MtCO2/MWh when replacing mainly gas and up to 0.7 MtCO2/MWh when replacing mainly coal powered generation. The paper focuses on CO2 emissions from power system operation phase, but long term impacts are shortly discussed.

Long-term urban carbon dioxide observations reveal spatial and temporal dynamics related to urban characteristics and growth

DOE PAGES

Mitchell, Logan E.; Lin, John C.; Bowling, David R.; ...

2018-03-05

Cities are concentrated areas of CO 2 emissions and have become the foci of policies for mitigation actions. However, atmospheric measurement networks suitable for evaluating urban emissions over time are scarce. Here we present a unique long-term (decadal) record of CO 2 mole fractions from five sites across Utah’s metropolitan Salt Lake Valley. We examine “excess” CO 2 above background conditions resulting from local emissions and meteorological conditions. We ascribe CO 2 trends to changes in emissions, since we did not find longterm trends in atmospheric mixing proxies. Three contrasting CO 2 trends emerged across urban types: negative trends atmore » a residentialindustrial site, positive trends at a site surrounded by rapid suburban growth, and relatively constant CO 2 over time at multiple sites in the established, residential, and commercial urban core. Analysis of populationwithin the atmospheric footprints of the different sites reveals approximately equal increases in population influencing the observed CO 2, implying a nonlinear relationshipwith CO 2 emissions: Population growth in rural areas that experienced suburban development was associated with increasing emissions while population growth in the developed urban core was associated with stable emissions. Four state-of-the-art global-scale emission inventories also have a nonlinear relationship with population density across the city; however, in contrast to our observations, they all have nearly constant emissions over time. Our results indicate that decadal scale changes in urban CO 2 emissions are detectable through monitoring networks and constitute a valuable approach to evaluate emission inventories and studies of urban carbon cycles.« less

Long-term urban carbon dioxide observations reveal spatial and temporal dynamics related to urban characteristics and growth

NASA Astrophysics Data System (ADS)

Mitchell, Logan E.; Lin, John C.; Bowling, David R.; Pataki, Diane E.; Strong, Courtenay; Schauer, Andrew J.; Bares, Ryan; Bush, Susan E.; Stephens, Britton B.; Mendoza, Daniel; Mallia, Derek; Holland, Lacey; Gurney, Kevin R.; Ehleringer, James R.

2018-03-01

Cities are concentrated areas of CO2 emissions and have become the foci of policies for mitigation actions. However, atmospheric measurement networks suitable for evaluating urban emissions over time are scarce. Here we present a unique long-term (decadal) record of CO2 mole fractions from five sites across Utah’s metropolitan Salt Lake Valley. We examine “excess” CO2 above background conditions resulting from local emissions and meteorological conditions. We ascribe CO2 trends to changes in emissions, since we did not find long-term trends in atmospheric mixing proxies. Three contrasting CO2 trends emerged across urban types: negative trends at a residential-industrial site, positive trends at a site surrounded by rapid suburban growth, and relatively constant CO2 over time at multiple sites in the established, residential, and commercial urban core. Analysis of population within the atmospheric footprints of the different sites reveals approximately equal increases in population influencing the observed CO2, implying a nonlinear relationship with CO2 emissions: Population growth in rural areas that experienced suburban development was associated with increasing emissions while population growth in the developed urban core was associated with stable emissions. Four state-of-the-art global-scale emission inventories also have a nonlinear relationship with population density across the city; however, in contrast to our observations, they all have nearly constant emissions over time. Our results indicate that decadal scale changes in urban CO2 emissions are detectable through monitoring networks and constitute a valuable approach to evaluate emission inventories and studies of urban carbon cycles.

Long-term urban carbon dioxide observations reveal spatial and temporal dynamics related to urban characteristics and growth

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

Mitchell, Logan E.; Lin, John C.; Bowling, David R.

Cities are concentrated areas of CO 2 emissions and have become the foci of policies for mitigation actions. However, atmospheric measurement networks suitable for evaluating urban emissions over time are scarce. Here we present a unique long-term (decadal) record of CO 2 mole fractions from five sites across Utah’s metropolitan Salt Lake Valley. We examine “excess” CO 2 above background conditions resulting from local emissions and meteorological conditions. We ascribe CO 2 trends to changes in emissions, since we did not find longterm trends in atmospheric mixing proxies. Three contrasting CO 2 trends emerged across urban types: negative trends atmore » a residentialindustrial site, positive trends at a site surrounded by rapid suburban growth, and relatively constant CO 2 over time at multiple sites in the established, residential, and commercial urban core. Analysis of populationwithin the atmospheric footprints of the different sites reveals approximately equal increases in population influencing the observed CO 2, implying a nonlinear relationshipwith CO 2 emissions: Population growth in rural areas that experienced suburban development was associated with increasing emissions while population growth in the developed urban core was associated with stable emissions. Four state-of-the-art global-scale emission inventories also have a nonlinear relationship with population density across the city; however, in contrast to our observations, they all have nearly constant emissions over time. Our results indicate that decadal scale changes in urban CO 2 emissions are detectable through monitoring networks and constitute a valuable approach to evaluate emission inventories and studies of urban carbon cycles.« less

Tidal variability of CO2 and CH4 emissions from the water column within a Rhizophora mangrove forest (New Caledonia).

PubMed

Jacotot, Adrien; Marchand, Cyril; Allenbach, Michel

2018-08-01

We performed a preliminary study to quantify CO 2 and CH 4 emissions from the water column within a Rhizophora spp. mangrove forest. Mean CO 2 and CH 4 emissions during the studied period were 3.35±3.62mmolCm -2 h -1 and 18.30±27.72μmolCm -2 h -1 , respectively. CO 2 and CH 4 emissions were highly variable and mainly driven by tides (flow/ebb, water column thickness, neap/spring). Indeed, an inverse relationship between the magnitude of the emissions and the thickness of the water column above the mangrove soil was observed. δ 13 CO 2 values ranged from -26.88‰ to -8.6‰, suggesting a mixing between CO 2 -enriched pore waters and lagoon incoming waters. In addition, CO 2 and CH 4 emissions were significantly higher during ebb tides, mainly due to the progressive enrichment of the water column by diffusive fluxes as its residence time over the forest floor increased. Eventually, we observed higher CO 2 and CH 4 emissions during spring tides than during neap tides, combined to depleted δ 13 CO 2 values, suggesting a higher contribution of soil-produced gases to the emissions. These higher emissions may result from higher renewable of the electron acceptor and enhanced exchange surface between the soil and the water column. This study shows that CO 2 and CH 4 emissions from the water column were not negligible and must be considered in future carbon budgets in mangroves. Copyright © 2018 Elsevier B.V. All rights reserved.

CO2 Emissions Embodied in Interprovincial Electricity Transmissions in China.

PubMed

Qu, Shen; Liang, Sai; Xu, Ming

2017-09-19

Existing studies on the evaluation of CO 2 emissions due to electricity consumption in China are inaccurate and incomplete. This study uses a network approach to calculate CO 2 emissions of purchased electricity in Chinese provinces. The CO 2 emission factors of purchased electricity range from 265 g/kWh in Sichuan to 947 g/kWh in Inner Mongolia. We find that emission factors of purchased electricity in many provinces are quite different from the emission factors of electricity generation. This indicates the importance of the network approach in accurately reflecting embodied emissions. We also observe substantial variations of emissions factors of purchased electricity within subnational grids: the provincial emission factors deviate from the corresponding subnational-grid averages from -58% to 44%. This implies that using subnational-grid averages as required by Chinese government agencies can be quite inaccurate for reporting indirect CO 2 emissions of enterprises' purchased electricity. The network approach can improve the accuracy of the quantification of embodied emissions in purchased electricity and emission flows embodied in electricity transmission.

Behavioural impairment in reef fishes caused by ocean acidification at CO2 seeps

NASA Astrophysics Data System (ADS)

Munday, Philip L.; Cheal, Alistair J.; Dixson, Danielle L.; Rummer, Jodie L.; Fabricius, Katharina E.

2014-06-01

Experiments have shown that the behaviour of reef fishes can be seriously affected by projected future carbon dioxide (CO2) concentrations in the ocean. However, whether fish can acclimate to elevated CO2 over the longer term, and the consequences of altered behaviour on the structure of fish communities, are unknown. We used marine CO2 seeps in Papua New Guinea as a natural laboratory to test these questions. Here we show that juvenile reef fishes at CO2 seeps exhibit behavioural abnormalities similar to those seen in laboratory experiments. Fish from CO2 seeps were attracted to predator odour, did not distinguish between odours of different habitats, and exhibited bolder behaviour than fish from control reefs. High CO2 did not, however, have any effect on metabolic rate or aerobic performance. Contrary to expectations, fish diversity and community structure differed little between CO2 seeps and nearby control reefs. Differences in abundances of some fishes could be driven by the different coral community at CO2 seeps rather than by the direct effects of high CO2. Our results suggest that recruitment of juvenile fish from outside the seeps, along with fewer predators within the seeps, is currently sufficient to offset any negative effects of high CO2 within the seeps. However, continuous exposure does not reduce the effect of high CO2 on behaviour in natural reef habitat, and this could be a serious problem for fish communities in the future when ocean acidification becomes widespread as a result of continued uptake of anthropogenic CO2 emissions.

The Role of Environmental Driving Factors in Historical and Projected Carbon Dynamics of Wetland Ecosystems in Alaska.

PubMed

Lyu, Zhou; Genet, Hélène; He, Yujie; Zhuang, Qianlai; McGuire, A David; Bennett, Alec; Breen, Amy; Clein, Joy; Euskirchen, Eugénie S; Johnson, Kristofer; Kurkowski, Tom; Pastick, Neal J; Rupp, T Scott; Wylie, Bruce K; Zhu, Zhiliang

2018-05-29

Wetlands are critical terrestrial ecosystems in Alaska, covering ~177,000 km 2 , an area greater than all the wetlands in the remainder of the United States. To assess the relative influence of changing climate, atmospheric carbon dioxide (CO 2 ) concentration, and fire regime on carbon balance in wetland ecosystems of Alaska, a modeling framework that incorporates a fire disturbance model and two biogeochemical models was used. Spatially explicit simulations were conducted at 1 km-resolution for the historical period (1950-2009) and future projection period (2010-2099). Simulations estimated that wetland ecosystems of Alaska lost 175 Tg carbon (C) in the historical period. Ecosystem C storage in 2009 was 5556 Tg, with 89% of the C stored in soils. The estimated loss of C as CO 2 and biogenic methane (CH 4 ) emissions resulted in wetlands of Alaska increasing the greenhouse gas forcing of climate warming. Simulations for the projection period were conducted for six climate change scenarios constructed from two climate models forced under three CO 2 emission scenarios. Ecosystem C storage averaged among climate scenarios increased 3.94 TgC/yr by 2099, with variability among the simulations ranging from 2.02 to 4.42 TgC/yr. These increases were driven primarily by increases in net primary production (NPP) that were greater than losses from increased decomposition and fire. The NPP increase was driven by CO 2 fertilization (~5% per 100 ppmv increase) and by increases in air temperature (~1% per °C increase). Increases in air temperature were estimated to be the primary cause for a projected 47.7% mean increase in biogenic CH 4 emissions among the simulations (~15% per °C increase). Ecosystem CO 2 sequestration offset the increase in CH 4 emissions during the 21 st century to decrease the greenhouse gas forcing of climate warming. However, beyond 2100, we expect that this forcing will ultimately increase as wetland ecosystems transition from being a sink to a source of atmospheric CO 2 because of (1) decreasing sensitivity of NPP to increasing atmospheric CO 2 , (2) increasing availability of soil C for decomposition as permafrost thaws, and (3) continued positive sensitivity of biogenic CH 4 emissions to increases in soil temperature. This article is protected by copyright. All rights reserved. This article is protected by copyright. All rights reserved.

NEOWISE Reactivated Mission Cometary CO+CO2: Preliminary Results from Years 1 through 3

NASA Astrophysics Data System (ADS)

Bauer, James M.; Grav, Tommy; Mainzer, Amy K.; Kramer, Emily A.; Masiero, Joseph R.; Kelley, Michael S.; Nugent, Carrie R.; Sonnett, Sarah M.; Fernandez, Yanga R.; Lisse, Casey M.; Meech, Karen Jean; Rosser, Joshua David; Walker, Russell G.; Wright, Edward L.; NEOWISE Team

2017-10-01

NEOWISE has utilized the WISE spacecraft data to provided an unpresidented number of radiometrically determined diameters and mid-infrared photometric observations of small bodies. During the WISE prime mission (January 2010 - January 2011) over 158000 solar system objects were detected by the spacecraft[1] before it was placed in hibernation in February of 2011. Of these, 164 comets were detected and characterized with respect to their dust production and particle size[2,3], CO+CO2 production[4], and diameters[5].The WISE spacecraft was reactived in 2013 and survey operations were restarted with the express purpose of searching for and characterizing solar system objects[6]. Re-named NEOWISE, the spacecraft continues to image the sky for Near-Earth objects and other small bodies at wavelengths of 3.4 and 4.6 μm, and is now into year 4 of its reactivated survey. The first 3 years of the NEOWISE reactivated mission produced detections of 11,800 objects[7,8], with a larger fraction of comets than during the cryogenic mission. Over 110 comets have been detected in the first 3 years of the reactivated survey. With NEOWISE's wavelength coverage, the survey is sensative to CO2 emission lines that are obscured by Earth's atmosphere and faint CO emission that is not easily detected from groundbased observations. We will present a preliminary analysis of this 3-year data set of comets regarding CO and CO2 production rates, tracing the behavior of these emissions at different heliocentric distances for several comets and for the ensemble of comets that show excess emission relative to dust that is indicative of CO+CO2 emission, approximately two thirds of the entire sample. We will also place these in the context of the Spitzer mission data set of targeted comet observations[9].[1] Mainzer, A. et al. 2011a, ApJ, 731, 53.[2] Kramer, E. 2014, PhD Dissertation, Univ. Central Florida.[3] Kramer, E. et al. 2017, ApJ, 838, 58.[4] Bauer, J. M. et al. 2015, ApJ, 814, 85.[5] Bauer, J. M. et al. 2017, J, 154, 53.[6] Mainzer, A. et al. 2014, ApJ, 792, 30.[7] Cutri, R. M. et al. 2017 (http://wise2.ipac.caltech.edu/docs/release/neowise/expsup)[8] Masiero, J. et al. 2017, submitted.[9] Kelley, M. S. et al. 2017, AAS DPS meeting.

Carbon dioxide emission factors for U.S. coal by origin and destination

USGS Publications Warehouse

Quick, J.C.

2010-01-01

This paper describes a method that uses published data to calculate locally robust CO2 emission factors for U.S. coal. The method is demonstrated by calculating CO2 emission factors by coal origin (223 counties, in 1999) and destination (479 power plants, in 2005). Locally robust CO2 emission factors should improve the accuracy and verification of greenhouse gas emission measurements from individual coal-fired power plants. Based largely on the county origin, average emission factors for U.S. lignite, subbituminous, bituminous, and anthracite coal produced during 1999 were 92.97,91.97,88.20, and 98.91 kg CO2/GJgross, respectively. However, greater variation is observed within these rank classes than between them, which limits the reliability of CO2 emission factors specified by coal rank. Emission factors calculated by destination (power plant) showed greater variation than those listed in the Emissions & Generation Resource Integrated Database (eGRID), which exhibit an unlikely uniformity that is inconsistent with the natural variation of CO2 emission factors for U.S. coal. ?? 2010 American Chemical Society.

The Carbon Dioxide Removal Model Intercomparison Project (CDRMIP): rationale and experimental protocol for CMIP6

NASA Astrophysics Data System (ADS)

Keller, David P.; Lenton, Andrew; Scott, Vivian; Vaughan, Naomi E.; Bauer, Nico; Ji, Duoying; Jones, Chris D.; Kravitz, Ben; Muri, Helene; Zickfeld, Kirsten

2018-03-01

The recent IPCC reports state that continued anthropogenic greenhouse gas emissions are changing the climate, threatening severe, pervasive and irreversible impacts. Slow progress in emissions reduction to mitigate climate change is resulting in increased attention to what is called geoengineering, climate engineering, or climate intervention - deliberate interventions to counter climate change that seek to either modify the Earth's radiation budget or remove greenhouse gases such as CO2 from the atmosphere. When focused on CO2, the latter of these categories is called carbon dioxide removal (CDR). Future emission scenarios that stay well below 2 °C, and all emission scenarios that do not exceed 1.5 °C warming by the year 2100, require some form of CDR. At present, there is little consensus on the climate impacts and atmospheric CO2 reduction efficacy of the different types of proposed CDR. To address this need, the Carbon Dioxide Removal Model Intercomparison Project (or CDRMIP) was initiated. This project brings together models of the Earth system in a common framework to explore the potential, impacts, and challenges of CDR. Here, we describe the first set of CDRMIP experiments, which are formally part of the 6th Coupled Model Intercomparison Project (CMIP6). These experiments are designed to address questions concerning CDR-induced climate reversibility, the response of the Earth system to direct atmospheric CO2 removal (direct air capture and storage), and the CDR potential and impacts of afforestation and reforestation, as well as ocean alkalinization.>

CO2 emissions from permafrost regions in Alaska during the nongrowing seasons

NASA Astrophysics Data System (ADS)

Natali, S.; Risk, D. A.; Minions, C.; Ludwig, S.; Watts, J. D.; Rogers, B. M.; Goetz, S. J.; Jastrow, J. D.; Jorgenson, T.; Schade, J. D.

2017-12-01

Surface air temperatures in the Arctic have been increasing twice as fast as the global average, and climate models project that this rate of warming will continue through the century, with the greatest warming occurring during the winter months. An increase in wintertime temperature may reduce belowground carbon storage due to enhanced microbial respiration during the snow-covered period when plant carbon uptake has predominantly ceased. Carbon emissions during the nongrowing season (NGS: i.e., autumn, winter and spring) are an important component of annual respiratory loss, yet there are large uncertainties in local and regional estimates of NGS CO2 fluxes. To address these uncertainties, we established a network of automated soil respiration sensors that run throughout the year at 10 locations across AK, including several paired burned and unburned sites in tundra and boreal regions. We measured soil CO2 flux, soil temperature (15, 50, 100 cm), soil moisture, and snow depth throughout the NGS, and plant cover, stand density, organic layer depth and thaw depth, and we analyzed active layer soils for total C and N, and organic matter composition. During spring thaw, all sites exhibited a strong pulse of CO2, a result of physical release of CO2 produced during the NGS. CO2 flux rates during the spring thaw were 1-2 orders of magnitude higher than winter CO2 fluxes and twice as high as fluxes during the early growing season. While temperature was a key driver of NGS fluxes across sites, our results suggest that soil organic matter content and composition were also important for NGS CO2 production. Despite warmer soils in burned spruce forests (Nome Creek, 2004 burn and Hess Creek, 2003 burn; 1-2 C warmer at 50-100 cm) compared to mature forests, NGS fluxes were either not significantly different or were higher in the mature stands than in burned stands, which may be a result of substrate limitation to NGS fluxes following fire. Quantifying the magnitude and drivers of NGS CO2 flux is critical for determining whether the Arctic is currently a source or sink for carbon and how this is likely to change as warming continues.

GHG and black carbon emission inventories from Mezquital Valley: The main energy provider for Mexico Megacity.

PubMed

Montelongo-Reyes, M M; Otazo-Sánchez, E M; Romo-Gómez, C; Gordillo-Martínez, A J; Galindo-Castillo, E

2015-09-15

The greenhouse gases and black carbon emission inventory from IPCC key category Energy was accomplished for the Mezquital Valley, one of the most polluted regions in Mexico, as the Mexico City wastewater have been continuously used in agricultural irrigation for more than a hundred years. In addition, thermoelectric, refinery, cement and chemistry industries are concentrated in the southern part of the valley, near Mexico City. Several studies have reported air, soil, and water pollution data and its main sources for the region. Paradoxically, these sources contaminate the valley, but boosted its economic development. Nevertheless, no research has been done concerning GHG emissions, or climate change assessment. This paper reports inventories performed by the 1996 IPCC methodology for the baseline year 2005. Fuel consumption data were derived from priority sectors such as electricity generation, refineries, manufacturing & cement industries, transportation, and residential use. The total CO2 emission result was 13,894.9 Gg, which constituted three-quarters of Hidalgo statewide energy category. The principal CO2 sources were energy transformation (69%) and manufacturing (19%). Total black carbon emissions were estimated by a bottom-up method at 0.66 Gg. The principal contributor was on-road transportation (37%), followed by firewood residential consumption (26%) and cocked brick manufactures (22%). Non-CO2 gas emissions were also significant, particularly SO2 (255.9 Gg), which accounts for 80% of the whole Hidalgo State emissions. Results demonstrated the negative environmental impact on Mezquital Valley, caused by its role as a Megacity secondary fuel and electricity provider, as well as by the presence of several cement industries. Copyright © 2015 Elsevier B.V. All rights reserved.

Effects of soil water content and elevated CO2 concentration on the monoterpene emission rate of Cryptomeria japonica.

PubMed

Mochizuki, Tomoki; Amagai, Takashi; Tani, Akira

2018-09-01

Monoterpenes emitted from plants contribute to the formation of secondary pollution and affect the climate system. Monoterpene emission rates may be affected by environmental changes such as increasing CO 2 concentration caused by fossil fuel burning and drought stress induced by climate change. We measured monoterpene emissions from Cryptomeria japonica clone saplings grown under different CO 2 concentrations (control: ambient CO 2 level, elevated CO 2 : 1000μmolmol -1 ). The saplings were planted in the ground and we did not artificially control the SWC. The relationship between the monoterpene emissions and naturally varying SWC was investigated. The dominant monoterpene was α-pinene, followed by sabinene. The monoterpene emission rates were exponentially correlated with temperature for all measurements and normalized (35°C) for each measurement day. The daily normalized monoterpene emission rates (E s0.10 ) were positively and linearly correlated with SWC under both control and elevated CO 2 conditions (control: r 2 =0.55, elevated CO 2 : r 2 =0.89). The slope of the regression line of E s0.10 against SWC was significantly higher under elevated CO 2 than under control conditions (ANCOVA: P<0.01), indicating that the effect of CO 2 concentration on monoterpene emission rates differed by soil water status. The monoterpene emission rates estimated by considering temperature and SWC (Improved G93 algorithm) better agreed with the measured monoterpene emission rates, when compared with the emission rates estimated by considering temperature alone (G93 algorithm). Our results demonstrated that the combined effects of SWC and CO 2 concentration are important for controlling the monoterpene emissions from C. japonica clone saplings. If these relationships can be applied to the other coniferous tree species, our results may be useful to improve accuracy of monoterpene emission estimates from the coniferous forests as affected by climate change in the present and foreseeable future. Copyright © 2018 Elsevier B.V. All rights reserved.

Simulating the dispersion of NOx and CO2 in the city of Zurich at building resolving scale

NASA Astrophysics Data System (ADS)

Brunner, Dominik; Berchet, Antoine; Emmenegger, Lukas; Henne, Stephan; Müller, Michael

2017-04-01

Cities are emission hotspots for both greenhouse gases and air pollutants. They contribute about 70% of global greenhouse gas emissions and are home to a growing number of people potentially suffering from poor air quality in the urban environment. High-resolution atmospheric transport modelling of greenhouse gases and air pollutants at the city scale has, therefore, several important applications such as air pollutant exposure assessment, air quality forecasting, or urban planning and management. When combined with observations, it also has the potential to quantify emissions and monitor their long-term trends, which is the main motivation for the deployment of urban greenhouse gas monitoring networks. We have developed a comprehensive atmospheric modeling model system for the city of Zurich, Switzerland ( 600,000 inhabitants including suburbs), which is composed of the mesoscale model GRAMM simulating the flow in a larger domain around Zurich at 100 m resolution, and the nested high-resolution model GRAL simulating the flow and air pollutant dispersion in the city at building resolving (5-10 m) scale. Based on an extremely detailed emission inventory provided by the municipality of Zurich, we have simulated two years of hourly NOx and CO2 concentration fields across the entire city. Here, we present a detailed evaluation of the simulations against a comprehensive network of continuous monitoring sites and passive samplers for NOx and analyze the sensitivity of the results to the temporal variability of the emissions. Furthermore, we present first simulations of CO2 and investigate the challenges associated with CO2 sources not covered by the inventory such as human respiration and exchange fluxes with urban vegetation.

Life cycle assessment of coal-fired power plants and sensitivity analysis of CO2 emissions from power generation side

NASA Astrophysics Data System (ADS)

Yin, Libao; Liao, Yanfen; Zhou, Lianjie; Wang, Zhao; Ma, Xiaoqian

2017-05-01

The life cycle assessment and environmental impacts of a 1000MW coal-fired power plant were carried out in this paper. The results showed that the operation energy consumption and pollutant emission of the power plant are the highest in all sub-process, which accounts for 93.93% of the total energy consumption and 92.20% of the total emission. Compared to other pollutant emissions from the coal-fired power plant, CO2 reached up to 99.28%. Therefore, the control of CO2 emission from the coal-fired power plants was very important. Based on the BP neural network, the amount of CO2 emission from the generation side of coal-fired power plants was calculated via carbon balance method. The results showed that unit capacity, coal quality and unit operation load had great influence on the CO2 emission from coal-fired power plants in Guangdong Province. The use of high volatile and high heat value of coal also can reduce the CO2 emissions. What’s more, under higher operation load condition, the CO2 emissions of 1 kWh electric energy was less.

Plastic-film mulching and urea types affect soil CO2 emissions and grain yield in spring maize on the Loess Plateau, China

NASA Astrophysics Data System (ADS)

Liu, Qiaofei; Chen, Yu; Li, Weiwei; Liu, Yang; Han, Juan; Wen, Xiaoxia; Liao, Yuncheng

2016-06-01

A 2-year field experiment was conducted on maize (Zea mays L.) to explore effective ways to decrease soil CO2 emissions and increase grain yield. Treatments established were: (1) no mulching with urea, (2) no mulching with controlled release fertiliser (CRF), (3) transparent plastic-film mulching (PMt) with urea, (4) PMt with CRF, (5) black plastic-film mulching (PMb) with urea, and (6) PMb with CRF. During the early growth stages, soil CO2 emissions were noted as PMt > PMb > no mulching, and this order was reversed in the late growth stages. This trend was the result of topsoil temperature dynamics. There were no significant correlations noted between soil CO2 emissions and soil temperature and moisture. Cumulative soil CO2 emissions were higher for the PMt than for the PMb, and grain yield was higher for the PMb treatments than for the PMt or no mulching treatments. The CRF produced higher grain yield and inhibited soil CO2 emissions. Soil CO2 emissions per unit grain yield were lower for the BC treatment than for the other treatments. In conclusion, the use of black plastic-film mulching and controlled release fertiliser not only increased maize yield, but also reduced soil CO2 emissions.

Volcanic sulfur dioxide and carbon dioxide measurements using small unmanned aerial systems

NASA Astrophysics Data System (ADS)

Pieri, D. C.; Diaz, J. A.; Fladeland, M. M.; Bland, G.; Alan, A., Jr.; Alegria, O.; Buongiorno, M. F.; Christensen, L. E.; Corrales, E.; Linick, J.; Mouginis-Mark, P. J.; Ramsey, M. S.; Realmuto, V. J.; Schwandner, F. M.

2015-12-01

Volcanoes emit gases continuously with significant pre-post-eruption changes, mainly H2O and CO2, plus SO2, and others. The SO2/CO2 ratio changes within volcanic life cycles making it an indicator of oncoming eruption phases: it can dip weeks to months before eruptions, then increase, and decrease back to background after eruptions. Over the last five years, we have made an effort to develop small and inexpensive lighter-than-air and fixed wing unmanned aerial vehicle (UAV) platforms in Costa Rica at Turrialba Volcano. Turrialba is an appropriate natural laboratory to test and prove platforms and instrumentation in low-level steady state volcanogenic gas and aerosol emissions at moderate altitudes (<12Kft ASL), where good technical infrastructure exists, with good physical access to the volcano. Our program in Costa Rica includes: (1) systematic monitoring of Turrialba from orbit with the Advanced Spaceborne Thermal Emission and Reflection radiometer (ASTER), with its thermal infrared (TIR) camera for SO2 retrieval, and more recently with GOSAT and OCO-2 for CO2; (2) in situ observations from aerostats and UAVs during ASTER overpasses, and (3) reconciliation of the orbital results with in situ data to validate mass retrieval and transport models. As part of the NASA HyspIRI Preparatory Airborne Activities program, we will conduct similar observations at Kilauea volcano using small UAVs and for both SO2 and CO2 in situ. One of the salient characteristics of the long lived Kilauea eruptions since 1983 has been the emission of SO2 in significant amounts, generating environmental stresses on local inhabitants due to lowered air quality, and stress on vegetation. Kilauea volcanic plumes, as with Turrialba, are mainly gases and liquid--SO2 is hydrolyzed to H2SO4 and the resulting highly acidic liquid aerosol is termed "vog," an environmental health hazard. Measurement of the diffuse CO2 emissions at Kilauea will also be of interest. Such measurements at Turrialba, indicate summit CO2 concentrations of up to 4000ppmv, and flank CO2 values of up to1500ppmv. We will discuss our SO2 and CO2 results at Turrialba and in Italy, and plans for Hawaii. Work presented here was done, in part, under contract to the NASA Earth Surface and Interior Focus Area, at the Jet Propulsion Laboratory of the California Institute of Technology.

The impact of economic complexity on carbon emissions: evidence from France.

PubMed

Can, Muhlis; Gozgor, Giray

2017-07-01

This paper reanalyzes the determinants of the CO 2 emissions in France. For this purpose, it considers the unit root test with two structural breaks and a dynamic ordinary least squares estimation. The paper also considers the effects of the energy consumption and the economic complexity on CO 2 emissions. First, it is observed that the EKC hypothesis is valid in France. Second, the positive effect of the energy consumption on CO 2 emissions is obtained. Third, it is observed that a higher economic complexity suppresses the level of CO 2 emissions in the long run. The findings imply noteworthy environmental policy implications to decrease the level of CO 2 emissions in France.

Air quality and climate impacts of alternative bus technologies in Greater London.

PubMed

Chong, Uven; Yim, Steve H L; Barrett, Steven R H; Boies, Adam M

2014-04-15

The environmental impact of diesel-fueled buses can potentially be reduced by the adoption of alternative propulsion technologies such as lean-burn compressed natural gas (LB-CNG) or hybrid electric buses (HEB), and emissions control strategies such as a continuously regenerating trap (CRT), exhaust gas recirculation (EGR), or selective catalytic reduction with trap (SCRT). This study assessed the environmental costs and benefits of these bus technologies in Greater London relative to the existing fleet and characterized emissions changes due to alternative technologies. We found a >30% increase in CO2 equivalent (CO2e) emissions for CNG buses, a <5% change for exhaust treatment scenarios, and a 13% (90% confidence interval 3.8-20.9%) reduction for HEB relative to baseline CO2e emissions. A multiscale regional chemistry-transport model quantified the impact of alternative bus technologies on air quality, which was then related to premature mortality risk. We found the largest decrease in population exposure (about 83%) to particulate matter (PM2.5) occurred with LB-CNG buses. Monetized environmental and investment costs relative to the baseline gave estimated net present cost of LB-CNG or HEB conversion to be $187 million ($73 million to $301 million) or $36 million ($-25 million to $102 million), respectively, while EGR or SCRT estimated net present costs were $19 million ($7 million to $32 million) or $15 million ($8 million to $23 million), respectively.

Toluene emissions from plants

NASA Astrophysics Data System (ADS)

Heiden, A. C.; Kobel, K.; Komenda, M.; Koppmann, R.; Shao, M.; Wildt, J.

The emission of toluene from different plants was observed in continuously stirred tank reactors and in field measurements. For plants growing without stress, emission rates were low and ranged from the detection limit up to 2·10-16 mol·cm-2·s-1. Under conditions of stress, the emission rates exceeded 10-14 mol·cm-2·s-1. Exposure of sunflower (Helianthus annuus L. cv. Gigantheus) to 13CO2 resulted in 13C-labeling of the emitted toluene on a time scale of hours. Although no biochemical pathway for the production of toluene is known, these results indicate that toluene is synthesized by the plants. The emission rates of toluene from sunflower are dependent on nutrient supply and wounding. Since α-pinene emission rates are also influenced by these factors, toluene and α-pinene emissions show a high correlation. During pathogen attack on Scots pines (Pinus sylvestris L.) significant toluene emissions were observed. In this case emissions of toluene and α-pinene also show a good correlation. Toluene emissions were also found in field experiments with pines using branch enclosures.

Design and application of a mobile ground-based observatory for continuous measurements of atmospheric trace gas and criteria pollutant species

DOE PAGES

Bush, S. E.; Hopkins, F. M.; Randerson, J. T.; ...

2015-08-26

Ground-based measurements of atmospheric trace gas species and criteria pollutants are essential for understanding emissions dynamics across space and time. Gas composition in the lower 50 m of the atmosphere has the greatest direct impacts on human health as well as ecosystem processes; hence data at this level are necessary for addressing carbon-cycle- and public-health-related questions. However, such surface data are generally associated with stationary measurement towers, where spatial representation is limited due to the high cost of establishing and maintaining an extensive network of measurement stations. We describe here a compact mobile laboratory equipped to provide high-precision, high-frequency, continuous,more » on-road synchronous measurements of CO 2, CO, CH 4, H 2O, NO x, O 3, aerosol, meteorological, and geospatial position data. The mobile laboratory has been deployed across the western USA. In addition to describing the vehicle and its capacity, we present data that illustrate the use of the laboratory as a powerful tool for investigating the spatial structure of urban trace gas emissions and criteria pollutants at spatial scales ranging from single streets to whole ecosystem and regional scales. We assess the magnitude of known point sources of CH 4 and also identify fugitive urban CH 4 emissions. We illustrate how such a mobile laboratory can be used to better understand emissions dynamics and quantify emissions ratios associated with trace gas emissions from wildfire incidents. Lastly, we discuss additional mobile laboratory applications in health and urban metabolism.« less

Design and application of a mobile ground-based observatory for continuous measurements of atmospheric trace gas and criteria pollutant species

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

Bush, S. E.; Hopkins, F. M.; Randerson, J. T.

Ground-based measurements of atmospheric trace gas species and criteria pollutants are essential for understanding emissions dynamics across space and time. Gas composition in the lower 50 m of the atmosphere has the greatest direct impacts on human health as well as ecosystem processes; hence data at this level are necessary for addressing carbon-cycle- and public-health-related questions. However, such surface data are generally associated with stationary measurement towers, where spatial representation is limited due to the high cost of establishing and maintaining an extensive network of measurement stations. We describe here a compact mobile laboratory equipped to provide high-precision, high-frequency, continuous,more » on-road synchronous measurements of CO 2, CO, CH 4, H 2O, NO x, O 3, aerosol, meteorological, and geospatial position data. The mobile laboratory has been deployed across the western USA. In addition to describing the vehicle and its capacity, we present data that illustrate the use of the laboratory as a powerful tool for investigating the spatial structure of urban trace gas emissions and criteria pollutants at spatial scales ranging from single streets to whole ecosystem and regional scales. We assess the magnitude of known point sources of CH 4 and also identify fugitive urban CH 4 emissions. We illustrate how such a mobile laboratory can be used to better understand emissions dynamics and quantify emissions ratios associated with trace gas emissions from wildfire incidents. Lastly, we discuss additional mobile laboratory applications in health and urban metabolism.« less

Design and application of a mobile ground-based observatory for continuous measurements of atmospheric trace gas and criteria pollutant species

NASA Astrophysics Data System (ADS)

Bush, S. E.; Hopkins, F. M.; Randerson, J. T.; Lai, C.-T.; Ehleringer, J. R.

2015-08-01

Ground-based measurements of atmospheric trace gas species and criteria pollutants are essential for understanding emissions dynamics across space and time. Gas composition in the lower 50 m of the atmosphere has the greatest direct impacts on human health as well as ecosystem processes; hence data at this level are necessary for addressing carbon-cycle- and public-health-related questions. However, such surface data are generally associated with stationary measurement towers, where spatial representation is limited due to the high cost of establishing and maintaining an extensive network of measurement stations. We describe here a compact mobile laboratory equipped to provide high-precision, high-frequency, continuous, on-road synchronous measurements of CO2, CO, CH4, H2O, NOx, O3, aerosol, meteorological, and geospatial position data. The mobile laboratory has been deployed across the western USA. In addition to describing the vehicle and its capacity, we present data that illustrate the use of the laboratory as a powerful tool for investigating the spatial structure of urban trace gas emissions and criteria pollutants at spatial scales ranging from single streets to whole ecosystem and regional scales. We assess the magnitude of known point sources of CH4 and also identify fugitive urban CH4 emissions. We illustrate how such a mobile laboratory can be used to better understand emissions dynamics and quantify emissions ratios associated with trace gas emissions from wildfire incidents. Lastly, we discuss additional mobile laboratory applications in health and urban metabolism.

Environmental impact of minimally invasive surgery in the United States: an estimate of the carbon dioxide footprint.

PubMed

Power, Nicholas E; Silberstein, Jonathan L; Ghoneim, Tarek P; Guillonneau, Bertrand; Touijer, Karim A

2012-12-01

To attempt to quantitate the carbon footprint of minimally invasive surgery (MIS) through approximated scope 1 to 3 CO(2) emissions to identify its potential role in global warming. To estimate national usage, we determined the number of inpatient and outpatient MIS procedures using International Classification of Diseases, ninth revision-clinical modification codes for all MIS procedures in a 2009 sample collected in national databases. Need for surgery was considered essential, and therefore traditional open surgery was used as the comparator. Scope 1 (direct) CO(2) emissions resulting from CO(2) gas used for insufflation were based on both escaping procedural CO(2) and metabolic CO(2) eliminated via respiration. Scopes 2 and 3 (indirect) emissions related to capture, compression, and transportation of CO(2) to hospitals and the disposal of single-use equipment not used in open surgery were calculated. The total CO(2) emissions were calculated to be 355,924 tonnes/year. For perspective, if MIS in the United States was considered a country, it would rank 189 th on the United Nations 2008 list of countries' carbon emissions per year. Limitations include the inability to account for uncertainty using the various models and tools for approximating CO(2) emissions. CO(2) emission of MIS in the United States may have a significant environmental impact. This is the first attempt to quantify CO(2) emissions related to MIS in the United States. Strategies for reduction, while maintaining high quality medical care, should be considered.

The change of CO2 emission on manufacturing sectors in Indonesia: An input-output analysis

NASA Astrophysics Data System (ADS)

Putranti, Titi Muswati; Imansyah, Muhammad Handry

2017-12-01

The objective of this paper is to evaluate the change of CO2 emission on manufacturing sectors in Indonesia using input-output analysis. The method used supply perspective can measure the impact of an increase in the value added of different productive on manufacturing sectors on total CO2 emission and can identify the productive sectors responsible for the increase in CO2 emission when there is an increase in the value added of the economy. The data used are based on Input-Output Energy Table 1990, 1995 and 2010. The method applied the elasticity of CO2 emission to value added. Using the elasticity approach, one can identify the highest elasticity on manufacturing sector as the change of value added provides high response to CO2 emission. Therefore, policy maker can concentrate on manufacturing sectors with the high response of CO2 emission due to the increase of value added. The approach shows the contribution of the various sectors that deserve more consideration for mitigation policy. Five of highest elasticity of manufacturing sectors of CO2 emission are Spinning & Weaving, Other foods, Tobacco, Wearing apparel, and other fabricated textiles products in 1990. Meanwhile, the most sensitive sectors Petroleum refinery products, Other chemical products, Timber & Wooden Products, Iron & Steel Products and Other non-metallic mineral products in 1995. Two sectors of the 1990 were still in the big ten, i.e. Spinning & weaving and Other foods in 1995 for the most sensitive sectors. The six sectors of 1995 in the ten highest elasticity of CO2 emission on manufacturing which were Plastic products, Other chemical products,Other fabricated metal products, Cement, Iron & steel products, Iron & steel, still existed in 2010 condition. The result of this research shows that there is a change in the most elastic CO2 emission of manufacturing sectors which tends from simple and light manufacturing to be a more complex and heavier manufacturing. Consequently, CO2 emission jumped significantly.

Ambient particulate matter and carbon monoxide at an urban site of India: Influence of anthropogenic emissions and dust storms.

PubMed

Yadav, Ravi; Sahu, L K; Beig, G; Tripathi, Nidhi; Jaaffrey, S N A

2017-06-01

Continuous measurements of PM 2.5 , PM 10 and CO were conducted at an urban site of Udaipur in India from April 2011 to March 2012. The annual mean concentrations of PM 2.5, PM 10 and CO were 42 ± 17 μg m -3 , 114 ± 31 μg m -3 and 343 ± 136 ppbv, respectively. Concentrations of both particulate and CO showed high values during winter/pre-monsoon (dry) period and lowest in the monsoon season (wet). Local anthropogenic emission and long-range transport from open biomass burning sources along with favourable synoptic meteorology led to elevated levels of pollutants in the dry season. However, higher values of PM 10 /PM 2.5 ratio during pre-monsoon season were caused by the episodes of dust storm. In the monsoon season, flow of cleaner air, rainfall and negligible emissions from biomass burning resulted in the lowest levels of pollutants. The concentrations of PM 2.5 , PM 10 and CO showed highest values during morning and evening rush hours, while lowest in the afternoon hours. In winter season, reductions of PM 2.5, CO and PM 10 during weekends were highest of 15%, 13% and 9%, respectively. In each season, the highest PM 2.5 /PM 10 ratio coincided with the highest concentrations of pollutants (CO and NO X ) indicating predominant emissions from anthropogenic sources. Exceptionally high concentrations of PM 10 during the episode of dust storm were due to transport from the Arabian Peninsula and Thar Desert. Up to ∼32% enhancements of PM 10 were observed during strong dust storms. Relatively low levels of O 3 and NO x during the storm periods indicate the role of heterogeneous removal. Copyright © 2017 Elsevier Ltd. All rights reserved.

Interannual variability in CO2 and CH4 exchange in a brackish tidal marsh in Northern California

NASA Astrophysics Data System (ADS)

Knox, S. H.; Windham-Myers, L.; Anderson, F. E.; Bergamaschi, B. A.

2017-12-01

Carbon (C) cycling in coastal wetlands is difficult to measure and model due to extremely dynamic atmospheric and hydrologic fluxes, as well as sensitivities to dynamic land- and ocean-based drivers. To date, few studies have begun continuous measurements of net ecosystem CO2 exchange (NEE) in these systems, and as such our understanding of the key drivers of NEE in coastal wetlands remain poorly understood. Recent eddy covariance measurements of NEE in these environments show considerable variability both within and across sites, with daily CO2 uptake and annual net CO2 budgets varying by nearly an order of magnitude between years and across locations. Furthermore, measurements of CH4 fluxes in these systems are even more limited, despite the potential for CH4 emissions from brackish and freshwater coastal wetlands. Here we present 3 years of near-continuous eddy covariance measurements of CO2 and CH4 fluxes from a brackish tidal marsh in Northern California and explore the drivers of interannual variability in CO2 and CH4 exchange. CO2 fluxes showed significant interannual variability; net CO2 uptake was near-zero in 2014 (6 ± 26 g C-CO2 m-2 yr-1), while much greater uptake was observed in 2015 and 2016 (209 ± 27 g C- CO2 m-2 yr-1 and 243 ± 26 g C-CO2 m-2 yr-1, respectively). Conversely, annual CH4 emissions were small and consistent across years, with the wetland emitting on average 1 ± 0.1 g C-CH4 m-2 yr-1. With respect to the net atmospheric GHG budget (assuming a sustained global warming potential (SGWP) of 45, expressed in units of CO2 equivalents), the wetland was near neutral in 2014, but a net GHG sink of 706 ± 105 g CO2 eq m-2 yr-1 and 836 ± 83 g CO2 eq m-2 yr-1 in 2015 and 2016, respectively. The large interannual variability in CO2 exchange was driven by notable year-to-year differences in temperature and precipitation as California experienced a severe drought and record high temperatures from 2012 to 2015. The large interannual variability in NEE and GHG budgets observed in this study emphasizes the need for long-term measurements of C fluxes in coastal wetlands, particularly under changing climatic conditions.

Temperature sensitivity of soil carbon dioxide and nitrous oxide emissions in mountain forest and meadow ecosystems in China

NASA Astrophysics Data System (ADS)

Zhang, Junjun; Peng, Changhui; Zhu, Qiuan; Xue, Wei; Shen, Yan; Yang, Yanzheng; Shi, Guohua; Shi, Shengwei; Wang, Meng

2016-10-01

An incubation experiment was conducted at three temperature levels (8, 18 and 28 °C) to quantify the response of soil CO2 and N2O emissions to temperature in three ecosystems (pine forest, oak forest, and meadow) located in the Qinling Mountains of China, which are considered to be susceptible to disturbance and climate changes, especially global warming. The soil CO2 emission rates increased with temperature and decreased with soil depth; they were the highest in the oak forest (broadleaf forest) and were lower in the pine forest (coniferous forest) and the meadow ecosystem. However, there was no significant difference in the soil N2O emission rates among the three ecosystems. The temperature sensitivity of CO2 and N2O was higher in the forest than in the meadow ecosystem. The Q10 values (temperature sensitivity coefficient) for CO2 and N2O were 1.07-2.25 and 0.82-1.22, respectively, for the three ecosystems. There was also evidence that the CO2 and N2O emission rates were positively correlated. The soil characteristics exhibited different effects on CO2 and N2O emissions among different ecosystems at the three temperature levels. Moreover, the soil dissolved organic carbon (DOC), specific ultraviolet absorbance (SUVA) and nitrate (NO3-) were important factors for CO2 emissions, whereas the soil ammonium (NH4+) and pH were the major controllers of N2O emissions. Unexpectedly, our results indicated that CO2 emissions are more sensitive to increasing temperature than N2O, noting the different feedback of CO2 and N2O emissions to global warming in this region. The different responses of greenhouse gas emissions in different forest types and a meadow ecosystem suggest that it is critical to conduct a comprehensive investigation of the complex mountain forest and meadow ecosystem in the transitional climate zone under global warming. Our research results provide new insight and advanced understanding of the variations in major greenhouse gas emissions (CO2 and N2O) and soil characteristics in response to warming.

CO in Protostars (COPS): Herschel-SPIRE Spectroscopy of Embedded Protostars

NASA Astrophysics Data System (ADS)

Yang, Yao-Lun; Green, Joel D.; Evans, Neal J., II; Lee, Jeong-Eun; Jørgensen, Jes K.; Kristensen, Lars E.; Mottram, Joseph C.; Herczeg, Gregory; Karska, Agata; Dionatos, Odysseas; Bergin, Edwin A.; Bouwman, Jeroen; van Dishoeck, Ewine F.; van Kempen, Tim A.; Larson, Rebecca L.; Yıldız, Umut A.

2018-06-01

We present full spectral scans from 200 to 670 μm of 26 Class 0+I protostellar sources obtained with Herschel-SPIRE as part of the “COPS-SPIRE” Open Time program, complementary to the DIGIT and WISH Key Programs. Based on our nearly continuous, line-free spectra from 200 to 670 μm, the calculated bolometric luminosities (L bol) increase by 50% on average, and the bolometric temperatures (T bol) decrease by 10% on average, in comparison with the measurements without Herschel. Fifteen protostars have the same class using T bol and L bol/L smm. We identify rotational transitions of CO lines from J=4\\to 3 to J=13\\to 12, along with emission lines of 13CO, HCO+, H2O, and [C I]. The ratios of 12CO to 13CO indicate that 12CO emission remains optically thick for J up < 13. We fit up to four components of temperature from the rotational diagram with flexible break points to separate the components. The distribution of rotational temperatures shows a primary population around 100 K with a secondary population at ∼350 K. We quantify the correlations of each line pair found in our data set and find that the strength of the correlation of CO lines decreases as the difference between J levels between two CO lines increases. The multiple origins of CO emission previously revealed by velocity-resolved profiles are consistent with this smooth distribution if each physical component contributes to a wide range of CO lines with significant overlap in the CO ladder. We investigate the spatial extent of CO emission and find that the morphology is more centrally peaked and less bipolar at high-J lines. We find the CO emission observed with SPIRE related to outflows, which consists of two components, the entrained gas and shocked gas, as revealed by our rotational diagram analysis, as well as the studies with velocity-resolved CO emission. Herschel is an ESA space observatory with science instruments provided by European-led Principal Investigator consortia and with important participation from NASA.

Greenhouse gas budget (CO2, CH4 and N2O) of intensively managed grassland following restoration.

PubMed

Merbold, Lutz; Eugster, Werner; Stieger, Jacqueline; Zahniser, Mark; Nelson, David; Buchmann, Nina

2014-06-01

The first full greenhouse gas (GHG) flux budget of an intensively managed grassland in Switzerland (Chamau) is presented. The three major trace gases, carbon dioxide (CO2), methane (CH4), and nitrous oxide (N2O) were measured with the eddy covariance (EC) technique. For CO2 concentrations, an open-path infrared gas analyzer was used, while N2O and CH4 concentrations were measured with a recently developed continuous-wave quantum cascade laser absorption spectrometer (QCLAS). We investigated the magnitude of these trace gas emissions after grassland restoration, including ploughing, harrowing, sowing, and fertilization with inorganic and organic fertilizers in 2012. Large peaks of N2O fluxes (20-50 nmol m(-2) s(-1) compared with a <5 nmol m(-2) s(-1) background) were observed during thawing of the soil after the winter period and after mineral fertilizer application followed by re-sowing in the beginning of the summer season. Nitrous oxide (N2O) fluxes were controlled by nitrogen input, plant productivity, soil water content and temperature. Management activities led to increased variations of N2O fluxes up to 14 days after the management event as compared with background fluxes measured during periods without management (<5 nmol m(-2) s(-1)). Fluxes of CO2 remained small until full plant development in early summer 2012. In contrast, methane emissions showed only minor variations over time. The annual GHG flux budget was dominated by N2O (48% contribution) and CO2 emissions (44%). CH4 flux contribution to the annual budget was only minor (8%). We conclude that recently developed multi-species QCLAS in an EC system open new opportunities to determine the temporal variation of N2O and CH4 fluxes, which further allow to quantify annual emissions. With respect to grassland restoration, our study emphasizes the key role of N2O and CO2 losses after ploughing, changing a permanent grassland from a carbon sink to a significant carbon source. © 2014 John Wiley & Sons Ltd.

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

PubMed

Sun, Zhihong; Niinemets, Ülo; Hüve, Katja; Rasulov, Bahtijor; Noe, Steffen M

2013-05-01

Effects of elevated atmospheric [CO2] on plant isoprene emissions are controversial. Relying on leaf-scale measurements, most models simulating isoprene emissions in future higher [CO2] atmospheres suggest reduced emission fluxes. However, combined effects of elevated [CO2] on leaf area growth, net assimilation and isoprene emission rates have rarely been studied on the canopy scale, but stimulation of leaf area growth may largely compensate for possible [CO2] inhibition reported at the leaf scale. This study tests the hypothesis that stimulated leaf area growth leads to increased canopy isoprene emission rates. We studied the dynamics of canopy growth, and net assimilation and isoprene emission rates in hybrid aspen (Populus tremula × Populus tremuloides) grown under 380 and 780 μmol mol(-1) [CO2]. A theoretical framework based on the Chapman-Richards function to model canopy growth and numerically compare the growth dynamics among ambient and elevated atmospheric [CO2]-grown plants was developed. Plants grown under elevated [CO2] had higher C : N ratio, and greater total leaf area, and canopy net assimilation and isoprene emission rates. During ontogeny, these key canopy characteristics developed faster and stabilized earlier under elevated [CO2]. However, on a leaf area basis, foliage physiological traits remained in a transient state over the whole experiment. These results demonstrate that canopy-scale dynamics importantly complements the leaf-scale processes, and that isoprene emissions may actually increase under higher [CO2] as a result of enhanced leaf area production. © 2013 The Authors. New Phytologist © 2013 New Phytologist Trust.

Uncertainty in projected climate change arising from uncertain fossil-fuel emission factors

NASA Astrophysics Data System (ADS)

Quilcaille, Y.; Gasser, T.; Ciais, P.; Lecocq, F.; Janssens-Maenhout, G.; Mohr, S.

2018-04-01

Emission inventories are widely used by the climate community, but their uncertainties are rarely accounted for. In this study, we evaluate the uncertainty in projected climate change induced by uncertainties in fossil-fuel emissions, accounting for non-CO2 species co-emitted with the combustion of fossil-fuels and their use in industrial processes. Using consistent historical reconstructions and three contrasted future projections of fossil-fuel extraction from Mohr et al we calculate CO2 emissions and their uncertainties stemming from estimates of fuel carbon content, net calorific value and oxidation fraction. Our historical reconstructions of fossil-fuel CO2 emissions are consistent with other inventories in terms of average and range. The uncertainties sum up to a ±15% relative uncertainty in cumulative CO2 emissions by 2300. Uncertainties in the emissions of non-CO2 species associated with the use of fossil fuels are estimated using co-emission ratios varying with time. Using these inputs, we use the compact Earth system model OSCAR v2.2 and a Monte Carlo setup, in order to attribute the uncertainty in projected global surface temperature change (ΔT) to three sources of uncertainty, namely on the Earth system’s response, on fossil-fuel CO2 emission and on non-CO2 co-emissions. Under the three future fuel extraction scenarios, we simulate the median ΔT to be 1.9, 2.7 or 4.0 °C in 2300, with an associated 90% confidence interval of about 65%, 52% and 42%. We show that virtually all of the total uncertainty is attributable to the uncertainty in the future Earth system’s response to the anthropogenic perturbation. We conclude that the uncertainty in emission estimates can be neglected for global temperature projections in the face of the large uncertainty in the Earth system response to the forcing of emissions. We show that this result does not hold for all variables of the climate system, such as the atmospheric partial pressure of CO2 and the radiative forcing of tropospheric ozone, that have an emissions-induced uncertainty representing more than 40% of the uncertainty in the Earth system’s response.

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

Effect of repeated drying-wetting-freezing-thawing cycles on the active soil organic carbon pool

NASA Astrophysics Data System (ADS)

Semenov, V. M.; Kogut, B. M.; Lukin, S. M.

2014-04-01

Samples of soddy-podzolic soil (long-term overgrown fallow and continuous bare fallow), gray forest soil (forest, farming agrocenosis), and a typical chernozem (virgin steppe, forest area, farming agrocenosis, continuous bare fallow) have been incubated under stable conditions; other samples of these soils have been subjected to six drying-wetting-incubation-freezing-thawing-incubation cycles during 136 days. The wetting of dried soils and the thawing of frozen soils result in an abrupt but short increase in the emission rate of C-CO2 by 2.7-12.4 and 1.6-2.7 times, respectively, compared to the stable incubation conditions. As the soil is depleted in potentially mineralizable organic matter, the rate of the C-CO2 emission pulses initiated by disturbing impacts decreases. The cumulative extra production of C-CO2 by soils of natural lands for six cycles makes up 21-40% of that in the treatments with stable incubation conditions; the corresponding value for cultivated soils, including continuous clean fallow, is in the range of 45-82%. The content of potentially mineralizable organic matter in the soils subjected to recurrent drying-wetting-freezingthawing cycles decreased compared to the soils without disturbing impacts by 1.6-4.4 times, and the mineralization constants decreased by 1.9-3.6 times. It has been emphasized that the cumulative effect of drying-wetting-freezing-thawing cycles is manifested not only in the decrease in the total Corg from the soil but also in the reduction of the mineralization potential of the soil organic matter.

Evaluation of On-Road Vehicle Emission Trends in the United States

NASA Astrophysics Data System (ADS)

Harley, R. A.; Dallmann, T. R.; Kirchstetter, T.

2010-12-01

Mobile sources contribute significantly to emissions of nitrogen oxides (NOx), carbon monoxide (CO), fine particulate matter (PM2.5), and black carbon (BC). These emissions lead to a variety of environmental problems including air pollution and climate change. At present, national and state-level mobile source emission inventories are developed using statistical models to predict emissions from large and diverse populations of vehicles. Activity is measured by total vehicle-km traveled, and pollutant emission factors are predicted based on laboratory testing of individual vehicles. Despite efforts to improve mobile source emission inventories, they continue to have large associated uncertainties. Alternate methods, such as the fuel-based approach used here, are needed to evaluate estimates of mobile source emissions and to help reduce uncertainties. In this study we quantify U.S. national emissions of NOx, CO, PM2.5, and BC from on-road diesel and gasoline vehicles for the years 1990-2010, including effects of a weakened national economy on fuel sales and vehicle travel from 2008-10. Pollutant emissions are estimated by multiplying total amounts of fuel consumed with emission factors expressed per unit of fuel burned. Fuel consumption is used as a measure of vehicle activity, and is based on records of taxable fuel sales. Pollutant emission factors are derived from roadside and tunnel studies, remote sensing measurements, and individual vehicle exhaust plume capture experiments. Emission factors are updated with new results from a summer 2010 field study conducted at the Caldecott tunnel in the San Francisco Bay Area.

40 CFR 63.1650 - Applicability and compliance dates.

Code of Federal Regulations, 2010 CFR

2010-07-01

... (CONTINUED) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS FOR SOURCE CATEGORIES National Emission... are major sources or are co-located at major sources of hazardous air pollutant emissions. (b) The following sources at a ferromanganese and silicomanganese production facility are subject to this subpart...

CO2, CO, and Hg emissions from the Truman Shepherd and Ruth Mullins coal fires, eastern Kentucky, USA

USGS Publications Warehouse

O'Keefe, Jennifer M.K.; Henke, Kevin R.; Hower, James C.; Engle, Mark A.; Stracher, Glenn B.; Stucker, J.D.; Drew, Jordan W.; Staggs, Wayne D.; Murray, Tiffany M.; Hammond, Maxwell L.; Adkins, Kenneth D.; Mullins, Bailey J.; Lemley, Edward W.

2010-01-01

Carbon dioxide (CO2), carbon monoxide (CO), and mercury (Hg) emissions were quantified for two eastern Kentucky coal-seam fires, the Truman Shepherd fire in Floyd County and the Ruth Mullins fire in Perry County. This study is one of the first to estimate gas emissions from coal fires using field measurements at gas vents. The Truman Shepherd fire emissions are nearly 1400 t CO2/yr and 16 kg Hg/yr resulting from a coal combustion rate of 450–550 t/yr. The sum of CO2 emissions from seven vents at the Ruth Mullins fire is 726 ± 72 t/yr, suggesting that the fire is consuming about 250–280 t coal/yr. Total Ruth Mullins fire CO and Hg emissions are estimated at 21 ± 1.8 t/yr and > 840 ± 170 g/yr, respectively. The CO2emissions are environmentally significant, but low compared to coal-fired power plants; for example, 3.9 × 106 t CO2/yr for a 514-MW boiler in Kentucky. Using simple calculations, CO2 and Hg emissions from coal-fires in the U.S. are estimated at 1.4 × 107–2.9 × 108 t/yr and 0.58–11.5 t/yr, respectively. This initial work indicates that coal fires may be an important source of CO2, CO, Hg and other atmospheric constituents.

Associations of individual, household and environmental characteristics with carbon dioxide emissions from motorised passenger travel

PubMed Central

Brand, Christian; Goodman, Anna; Rutter, Harry; Song, Yena; Ogilvie, David

2013-01-01

Carbon dioxide (CO2) emissions from motorised travel are hypothesised to be associated with individual, household, spatial and other environmental factors. Little robust evidence exists on who contributes most (and least) to travel CO2 and, in particular, the factors influencing commuting, business, shopping and social travel CO2. This paper examines whether and how demographic, socio-economic and other personal and environmental characteristics are associated with land-based passenger transport and associated CO2 emissions. Primary data were collected from 3474 adults using a newly developed survey instrument in the iConnect study in the UK. The participants reported their past-week travel activity and vehicle characteristics from which CO2 emissions were derived using an adapted travel emissions profiling method. Multivariable linear and logistic regression analyses were used to examine what characteristics predicted higher CO2 emissions. CO2 emissions from motorised travel were distributed highly unequally, with the top fifth of participants producing more than two fifth of emissions. Car travel dominated overall CO2 emissions, making up 90% of the total. The strongest independent predictors of CO2 emissions were owning at least one car, being in full-time employment and having a home-work distance of more than 10 km. Income, education and tenure were also strong univariable predictors of CO2 emissions, but seemed to be further back on the causal pathway than having a car. Male gender, late-middle age, living in a rural area and having access to a bicycle also showed significant but weaker associations with emissions production. The findings may help inform the development of climate change mitigation policies for the transport sector. Targeting individuals and households with high car ownership, focussing on providing viable alternatives to commuting by car, and supporting planning and other policies that reduce commuting distances may provide an equitable and efficient approach to meeting carbon mitigation targets. PMID:24882922

The travel-related carbon dioxide emissions of atmospheric researchers

NASA Astrophysics Data System (ADS)

Stohl, A.

2008-11-01

Most atmospheric scientists agree that greenhouse gas emissions have already caused significant changes to the global climate system and that these changes will accelerate in the near future. At the same time, atmospheric scientists who like other scientists rely on international collaboration and information exchange travel a lot and, thereby, cause substantial emissions of CO2. In this paper, the CO2 emissions of the employees working at an atmospheric research institute (the Norwegian Institute for Air Research, NILU) caused by all types of business travel (conference visits, workshops, field campaigns, instrument maintainance, etc.) were calculated for the years 2005 2007. It is estimated that more than 90% of the emissions were caused by air travel, 3% by ground travel and 5% by hotel usage. The travel-related annual emissions were between 1.9 and 2.4 t CO2 per employee or between 3.9 and 5.5 t CO2 per scientist. For comparison, the total annual per capita CO2 emissions are 4.5 t worldwide, 1.2 t for India, 3.8 t for China, 5.9 t for Sweden and 19.1 t for Norway. The travel-related CO2 emissions of a NILU scientist, occurring in 24 days of a year on average, exceed the global average annual per capita emission. Norway's per-capita CO2 emissions are among the highest in the world, mostly because of the emissions from the oil industry. If the emissions per NILU scientist derived in this paper are taken as representative for the average Norwegian researcher, travel by Norwegian scientists would nevertheless account for a substantial 0.2% of Norway's total CO2 emissions. Since most of the travel-related emissions are due to air travel, water vapor emissions, ozone production and contrail formation further increase the relative importance of NILU's travel in terms of radiative forcing.

The travel-related carbon dioxide emissions of atmospheric researchers

NASA Astrophysics Data System (ADS)

Stohl, A.

2008-04-01

Most atmospheric scientists agree that greenhouse gas emissions have already caused significant changes to the global climate system and that these changes will accelerate in the near future. At the same time, atmospheric scientists who - like other scientists - rely on international collaboration and information exchange travel a lot and, thereby, cause substantial emissions of carbon dioxide (CO2). In this paper, the CO2 emissions of the employees working at an atmospheric research institute (the Norwegian Institute for Air Research, NILU) caused by all types of business travel (conference visits, workshops, field campaigns, instrument maintainance, etc.) were calculated for the years 2005-2007. It is estimated that more than 90% of the emissions were caused by air travel, 3% by ground travel and 5% by hotel usage. The travel-related annual emissions were between 1.9 and 2.4 t CO2 per employee or between 3.9 and 5.5 t CO2 per scientist. For comparison, the total annual per capita CO2 emissions are 4.5 t worldwide, 1.2 t for India, 3.8 t for China, 5.9 t for Sweden and 19.1 t for Norway. The travel-related CO2 emissions of a NILU scientist, occurring in 24 days of a year on average, exceed the global average annual per capita emission. Norway's per-capita CO2 emissions are among the highest in the world, mostly because of the emissions from the oil industry. If the emissions per NILU scientist derived in this paper are taken as representative for the average Norwegian researcher, travel by Norwegian scientists would nevertheless account for a substantial 0.2% of Norway's total CO2 emissions. Since most of the travel-related emissions are due to air travel, water vapor emissions, ozone production and contrail formation further increase the relative importance of NILU's travel in terms of radiative forcing.

Quantifying direct carbon dioxide emissions from wastewater treatment units by nondispersive infrared sensor (NDIR) - A pilot study.

PubMed

Kosse, Pascal; Kleeberg, Tasja; Lübken, Manfred; Matschullat, Jörg; Wichern, Marc

2018-08-15

Treatment of nutrient-rich wastewater potentially results in direct release of greenhouse gases (GHGs) such as CO 2 , N 2 O or CH 4 - and thus affects Waste Water Treatment Plant's carbon footprint. Accurate CO 2 quantification is challenging due to various chemical, physical and operational conditions. A floating chamber equipped with a nondispersive infrared, single beam, dual wavelength sensor has been evaluated for a pilot approach to quantify fugitive CO 2 emissions above different wastewater treatment units. Total average CO 2 flux was 1182gCO 2 ·m -2 ·d -1 with minimum and maximum fluxes of 829gCO 2 ·m -2 ·d -1 and 1493gCO 2 ·m -2 ·d -1 , respectively. Total observed CO 2 emissions were in 7 to 17kgCO 2 ·PE -1 ·a -1 (average 12kgCO 2 ·PE -1 ·a -1 ). The nitrification tank accounted for about 94.3% of the emissions, followed by secondary clarification (ca. 4.3%) and denitrification (ca. 1.4%), based on those average annual CO 2 emissions per population equivalent (PE). Copyright © 2018 Elsevier B.V. All rights reserved.