Science.gov

Sample records for total annual emissions

  1. Estimation of total annual mercury emissions from cement manufacturing facilities in Korea

    NASA Astrophysics Data System (ADS)

    Won, Jong Hyun; Lee, Tai Gyu

    2012-12-01

    This study examined mercury (Hg) emissions from cement manufacturing facilities in Korea. Hg concentrations in stack gases from a kiln at the largest cement manufacturing facility (CMF) in Korea were measured using three different methods: a wet-chemical method and on-line measurements with two different types of conversion systems (SnCl2 and thermal) attached in front of each analyzer. The Hg concentrations of the feedstocks and fuels were then analyzed to determine the total amount of Hg input into CMFs and how much each material contributed to the Hg input. The total annual Hg input into all CMFs in Korea was estimated to be 1.71 tons, while the total annual Hg emissions estimated from the stack-gas measurement was 1.17-1.53 tons, indicating that 68-89% of total Hg input is released into the atmosphere. Therefore, more stringent regulation and effective control technologies should be applied to the CMFs to reduce Hg emissions.

  2. Anthropogenic mercury emission inventory with emission factors and total emission in Korea

    NASA Astrophysics Data System (ADS)

    Kim, Jeong-Hun; Park, Jung-Min; Lee, Sang-Bo; Pudasainee, Deepak; Seo, Yong-Chil

    2010-07-01

    Mercury emissions concentrations, emission factors, and the total national emission from major anthropogenic sources in Korea for the year 2007 were estimated. Uncontrolled and controlled mercury emission factors and the total emission from each source types are presented. The annual national mercury emission from major anthropogenic sources for the year 2007, on average was 12.8 ton which ranged from 6.5 to 20.2 ton. Averaged emissions of elemental, oxidized, and particulate mercury were estimated at 8.25 ton, 3.69 ton, and 0.87 ton, respectively. Due to the removal of a major portion of particulate and oxidized mercury species, elemental mercury was dominant in stack emission. About 54.8% of mercury emission was contributed by industrial sources, 45.0% by stationary combustion sources and 0.02% by mobile sources. Thermal power plants, oil refineries, cement kilns and incinerators (municipal, industrial, medical, sewage sludge) were the major mercury emitters, contributing about 26%, 25%, 21% and 20%, respectively to the total mercury emission. Other sources (crematory, pulp and paper manufacturing, nonferrous metals manufacturing, glass manufacturing) contributed about 8% of the total emission. Priority should be given in controlling mercury emissions from coal-fired power plants, oil refineries, cement kilns and waste incinerators. More measurements including natural and re-emission sources are to be carried out in the future in order to have a clear scenario of mercury emission from the country and to apply effective control measures.

  3. Soil respiration at mean annual temperature predicts annual total across vegetation types and biomes

    PubMed Central

    Bahn, M.; Reichstein, M.; Davidson, E. A.; Grnzweig, J.; Jung, M.; Carbone, M. S.; Epron, D.; Misson, L.; Nouvellon, Y.; Roupsard, O.; Savage, K.; Trumbore, S. E.; Gimeno, C.; Yuste, J. Curiel; Tang, J.; Vargas, R.; Janssens, I. A.

    2011-01-01

    Soil respiration (SR) constitutes the largest flux of CO2 from terrestrial ecosystems to the atmosphere. However, there still exist considerable uncertainties as to its actual magnitude, as well as its spatial and interannual variability. Based on a reanalysis and synthesis of 80 site-years for 57 forests, plantations, savannas, shrublands and grasslands from boreal to tropical climates we present evidence that total annual SR is closely related to SR at mean annual soil temperature (SRMAT), irrespective of the type of ecosystem and biome. This is theoretically expected for non water-limited ecosystems within most of the globally occurring range of annual temperature variability and sensitivity (Q10). We further show that for seasonally dry sites where annual precipitation (P) is lower than potential evapotranspiration (PET), annual SR can be predicted from wet season SRMAT corrected for a factor related to P/PET. Our finding indicates that it can be sufficient to measure SRMAT for obtaining a well constrained estimate of its annual total. This should substantially increase our capacity for assessing the spatial distribution of soil CO2 emissions across ecosystems, landscapes and regions, and thereby contribute to improving the spatial resolution of a major component of the global carbon cycle. PMID:23293656

  4. EVALUATION OF TOTAL ORGANIC EMISSIONS ANALYSIS METHODS

    EPA Science Inventory

    The rationale and supporting experimental data for revising EPA's 1996 "Guidance for Total Organics" are summarized in this document. It reports the results of reseach and investigation of improvements to the Total Organic Emissions (TOE) guidance used by EPA to measure recovera...

  5. Further Evaluation of an Emperical Equation for Annual Total Evaporation

    NASA Technical Reports Server (NTRS)

    Choudhury, Bhaskar J.

    1999-01-01

    An empirical equation for annual total evaporation based on annual precipitation and net radiation was found to provide evaporation within 10% of the observed values at seven locations within temperate and tropical regions, but it overestimated evaporation by 90% at one location within the tundra region. A synthesis of observations at two other locations within the tundra region gives overestimates of about 65%. A general analysis of observed precipitation, net radiation, and runoff within the tundra region shows that the empirical equation is generally biased to overestimate annual evaporation within the tundra region. A theoretical analysis is being done to understand the reason behind this bias.

  6. Contribution of evaporative emissions from gasoline vehicles toward total VOC emissions in Japan.

    PubMed

    Yamada, Hiroyuki

    2013-04-01

    The features of evaporative emissions from gasoline vehicles were examined. One potential source of evaporative emissions is mainly the so-called sigh of a fuel tank, which is a function of the daily temperature change and the volume not occupied by fuel. A theoretical equation was proposed for estimating the fuel vapor generation. It reproduced observed features well but underestimated the absolute values obtained in the experimental results. The widely used semi-empirical Reddy equation overestimates the results. The performance of a carbon canister was also evaluated. More than 95% of fuel vapor generation was trapped by the carbon canister. However, the canister worked for only one day because it adsorbed more VOC than that contained in the sigh alone. To estimate the evaporative emissions in the real world, the fuel tank temperature change while a car was parked in an outside car park was monitored and was found to be almost the same as the change in ambient air temperature; no other weather conditions had any effect. According to the findings in this study and data on frequency of car use, the annual amount of evaporative emissions from gasoline vehicles in Japan was estimated to be 4.6% of the total VOC emissions in Japan, making it the 6th-highest source of VOC. PMID:23422493

  7. Quantification of annual carbon emissions from deforestation in South America

    NASA Astrophysics Data System (ADS)

    Song, X.; Huang, C.; Townshend, J. R.

    2013-12-01

    Tropical deforestation is the second largest source of carbon emissions to the atmosphere and also one of the most uncertain components of the global carbon cycle. Current estimates of carbon emissions from deforestation have errors as much as ×50%. This substantial uncertainty range stems in part from the uncertain estimate of changes in forest area as well as the lack of spatially explicit information on biomass density. Here we use multiple sources satellite data to quantify carbon emissions from deforestation in South America on a year-to-year basis from 2000 to 2010. We first use time-series multi-spectral images to map the spatial extent of forest loss. We then spatially match the area of deforestation with initial biomass density to quantify the committed carbon emissions from forest loss. Our results reveal that the five countries with the highest deforestation related emissions in South America are Brazil, Bolivia, Colombia, Argentina, and Chile. Their average annual emission rates are 218 TgC/yr, 23 TgC/yr, 16 TgC/yr, 14 TgC/yr and 11 TgC/yr, respectively. However, there are substantial inter-annual variations. Emissions in both Brazil and Argentina increased initially until 2005, and then declined. But Bolivia had a steady increasing trend in its emission over the 10 years. The coefficient of variation of annual emissions in these five countries ranges from 36% to 45%, indicating considerable inter-annual variations in carbon emissions from deforestation in these countries. These spatially explicit, multi-year emission estimates may be used as a baseline for REDD+ or other related emission mitigation efforts. The trends and large inter-annual variations in deforestation related emissions as revealed in this study should be considered in evaluating the performance of such efforts.

  8. 40 CFR 57.303 - Total plantwide emission limitation.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... (CONTINUED) PRIMARY NONFERROUS SMELTER ORDERS Constant Controls and Related Requirements § 57.303 Total... requirement limiting the total allowable emissions from the smelter to the level which would have been associated with production at the smelter's maximum production capacity (as defined in § 57.103(r)) as...

  9. 40 CFR 57.303 - Total plantwide emission limitation.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... (CONTINUED) PRIMARY NONFERROUS SMELTER ORDERS Constant Controls and Related Requirements § 57.303 Total... requirement limiting the total allowable emissions from the smelter to the level which would have been associated with production at the smelter's maximum production capacity (as defined in § 57.103(r)) as...

  10. 40 CFR 57.303 - Total plantwide emission limitation.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... (CONTINUED) PRIMARY NONFERROUS SMELTER ORDERS Constant Controls and Related Requirements § 57.303 Total... requirement limiting the total allowable emissions from the smelter to the level which would have been associated with production at the smelter's maximum production capacity (as defined in § 57.103(r)) as...

  11. 40 CFR 57.303 - Total plantwide emission limitation.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... (CONTINUED) PRIMARY NONFERROUS SMELTER ORDERS Constant Controls and Related Requirements § 57.303 Total... requirement limiting the total allowable emissions from the smelter to the level which would have been associated with production at the smelter's maximum production capacity (as defined in § 57.103(r)) as...

  12. Hemispherical total emissivity of Hastelloy N with different surface conditions

    NASA Astrophysics Data System (ADS)

    Gordon, Andrew J.; Walton, Kyle L.; Ghosh, Tushar K.; Loyalka, Sudarshan K.; Viswanath, Dabir S.; Tompson, Robert V.

    2012-07-01

    The hemispherical total emissivity of Hastelloy N (a candidate structural material for Next Generation Nuclear Plants (NGNPs), particularly for the molten fluoride cooled reactors) was measured using an experimental set-up that was constructed in accordance with the standard ASTM C835-06. The material surface conditions included: (i) 'as received' (original) sample from the supplier; (ii) samples with increased surface roughness through sand blasting; (iii) oxidized surface, and (iv) samples coated with graphite powder. The emissivity of the as received samples varied from around 0.22 to 0.28 in the temperature range of 473 K to 1498 K. The emissivity increased when the roughness of the surface increased compared to an as received sample. When Hastelloy N was oxidized in air at 1153 K or coated with graphite powder, its emissivity increased substantially. The sample sand blasted with 60 grit beads and sprinkled with graphite powder showed an increase of emissivity from 0.2 to 0.60 at 473 K and from 0.25 to 0.67 at 1473 K. The oxidized surface showed a similar behavior: an increase in emissivity compared to an unoxidized sample. This increase in emissivity has strong favorable safety implications in terms of decay heat removal in post-accident environments. The data were compared with another Hastelloy family member, Hastelloy X.

  13. 29 CFR 779.253 - What is included in computing the total annual inflow volume.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... volume. 779.253 Section 779.253 Labor Regulations Relating to Labor (Continued) WAGE AND HOUR DIVISION... computing the total annual inflow volume. The goods which the establishment purchases or receives for resale that move or have moved across State lines must “amount in total annual volume to $250,000 or more.”...

  14. 29 CFR 779.253 - What is included in computing the total annual inflow volume.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... volume. 779.253 Section 779.253 Labor Regulations Relating to Labor (Continued) WAGE AND HOUR DIVISION... computing the total annual inflow volume. The goods which the establishment purchases or receives for resale that move or have moved across State lines must “amount in total annual volume to $250,000 or more.”...

  15. 29 CFR 779.253 - What is included in computing the total annual inflow volume.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... volume. 779.253 Section 779.253 Labor Regulations Relating to Labor (Continued) WAGE AND HOUR DIVISION... computing the total annual inflow volume. The goods which the establishment purchases or receives for resale that move or have moved across State lines must “amount in total annual volume to $250,000 or more.”...

  16. 29 CFR 779.253 - What is included in computing the total annual inflow volume.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 29 Labor 3 2010-07-01 2010-07-01 false What is included in computing the total annual inflow... computing the total annual inflow volume. The goods which the establishment purchases or receives for resale..., delivery, storage and any other will be included in computing the $250,000. The dollar volume of the...

  17. 29 CFR 779.253 - What is included in computing the total annual inflow volume.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 29 Labor 3 2011-07-01 2011-07-01 false What is included in computing the total annual inflow... computing the total annual inflow volume. The goods which the establishment purchases or receives for resale..., delivery, storage and any other will be included in computing the $250,000. The dollar volume of the...

  18. Continuous monitoring of total hydrocarbon emissions from sludge incinerators

    SciTech Connect

    Bostian, H.E.; Crumpler, E.P.; Koch, P.D.; Chehaske, J.T.; Hagele, J.C.

    1993-01-01

    The US Environmental Protection Agency (EPA), Office of Water (OW) drafted risk-based sludge regulations (for incineration and a variety of other options) under Section 405d of the Clean Water Act. Under consideration for the final regulation is a provision for continuously monitoring total hydrocarbon (THC) emissions as a method of controlling organic emissions from sludge incineration. The monitoring would have to demonstrate that the THC stack emissions were not exceeding a concentration limit. Continuous analyzers for THC, CO, and oxygen (O2) were installed and operated at two facilities, both of which employed multiple-hearth furnaces (MHFs) to incinerate wastewater sludge. In addition, EPA requested an evaluation of the use of these monitors to assist with incinerator operation.

  19. Global methane emissions from landfills: New methodology and annual estimates 1980-1996

    NASA Astrophysics Data System (ADS)

    Bogner, J.; Matthews, E.

    2003-06-01

    Significant interannual variations in the growth rate of atmospheric CH4 justify the development of an improved methodology for landfill emissions, the largest anthropogenic source in many developed countries. A major problem is that reliable solid waste data often do not exist, especially for developing countries where emissions are increasing. Here we develop and apply a new proxy method to reconstruct historical estimates for annual CH4 emissions for the period 1980-1996. Using composited solid waste data from 1975-1995, we developed linear regressions for waste generation per capita based on energy consumption per capita, a surrogate which reflects population and affluence, the major determinants of solid waste generation rates. Using total population (developed countries) or urban population (developing countries), annual landfill CH4 emissions were estimated using a modified Intergovernmental Panel on Climate Change (IPCC) methodology. Methane recovery was modeled by fitting historic data to time-dependent linear relationships. Two scenarios for global emissions using the surrogate were compared to two scenarios using an IPCC standard methodology. Results from all four scenarios range from 16 to 57 Tg CH4 yr-1, a similar range as previous estimates. We support the use of the lower energy surrogate scenario (A) with annual emissions of 16-20 Tg CH4 yr-1, both positive and negative annual variations, and commercial recovery >15% by 1996. The surrogate provides a reasonable methodology for a large number of countries where data do not exist, a consistent methodology for both developed and developing countries, and a procedure which facilitates annual updates using readily available data.

  20. Annual cycle of methane emission from a subarctic peatland

    NASA Astrophysics Data System (ADS)

    Jackowicz-KorczyńSki, Marcin; Christensen, Torben R.; BäCkstrand, Kristina; Crill, Patrick; Friborg, Thomas; Mastepanov, Mikhail; StröM, Lena

    2010-06-01

    Although much attention in recent years has been devoted to methane (CH4) emissions from northern wetlands, measurement based data sets providing full annual budgets are still limited in number. This study was designed to help fill the gap of year-round measurements of CH4 emissions from subarctic mires. We report continuous eddy correlation CH4 flux measurements made during 2006 and 2007 over the Stordalen mire in subarctic Sweden (68°20'N, 19°03'E, altitude 351 m) using a cryocooled tunable diode laser. The landscape-scale CH4 fluxes originated mainly from the permafrost free wet parts of the mire dominated by tall graminoid vegetation. The midseason average CH4 emission mean was 6.2 ± 2.6 mg m-2 h-1. A detailed footprint analysis indicates an additional strong influence on the flux by the nearby shallow Lake Villasjön (0.17 km2, maximum depth 1.3 m). A stable bimodal distribution of wind flow from either the east or the west allowed separating the lake and mire vegetation signals. The midseason lake emission rates were as high as 12.3 ± 3.3 mg m-2 h-1. Documented CH4 fluxes are similar to results obtained by automatic chamber technique and higher than manual chamber measurements made in the wet minerotrophic section dominated by Eriophorum angustifolium. The high fluxes observed from this vegetation type are significant because the areal distribution of this source in the mire is expanding due to ongoing thawing of the permafrost. A simple peat temperature relationship with CH4 emissions was used to fill data gaps to construct a complete annual budget of CH4 fluxes over the studied area. The calculated annual CH4 emissions in 2006 and 2007 equaled 24.5 and 29.5 g CH4 m-2 yr-1, respectively. The summer season CH4 emissions dominated (65%) the annual flux, with the shoulder seasons of spring and autumn significant (25%) and a minor flux from the winter (10%).

  1. 16 CFR 801.11 - Annual net sales and total assets.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 16 Commercial Practices 1 2010-01-01 2010-01-01 false Annual net sales and total assets. 801.11 Section 801.11 Commercial Practices FEDERAL TRADE COMMISSION RULES, REGULATIONS, STATEMENTS AND INTERPRETATIONS UNDER THE HART-SCOTT-RODINO ANTITRUST IMPROVEMENTS ACT OF 1976 COVERAGE RULES § 801.11 Annual...

  2. Measurement of total hemispherical emissivity of contaminated mirror surfaces

    NASA Technical Reports Server (NTRS)

    Facey, T. A.; Nonnenmacher, A. L.

    1989-01-01

    The effects of dust contamination on the total hemispherical emissivity (THE) of a 1.5-inch-diameter Al/MgF2-coated telescope mirror are investigated experimentally. The THE is determined by means of cooling-rate measurements in the temperature range 10-14.5 C in a vacuum of 100 ntorr or better. Photographs and drawings of the experimental setup are provided, and results for 11 dust levels are presented in tables and graphs. It is shown that dust has a significant effect on THE, but the experimental losses are only about half those predicted for perfectly black dust in perfect thermal contact with the mirror surface.

  3. 40 CFR 57.303 - Total plantwide emission limitation.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... the sum of uncontrolled process and fugitive emissions, and emissions from any control systems (operating at the efficiency prescribed under § 57.302). These emission rates may be derived from...

  4. Optimization of heavy metals total emission, case study: Bor (Serbia)

    NASA Astrophysics Data System (ADS)

    Ilić, Ivana; Bogdanović, Dejan; Živković, Dragana; Milošević, Novica; Todorović, Boban

    2011-07-01

    The town of Bor (Serbia) is one of the most polluted towns in southeastern Europe. The copper smelter which is situated in the centre of the town is the main pollutant, mostly because of its old technology, which leads to environmental pollution caused by higher concentrations of SO 2 and PM 10. These facts show that the word is about a very polluted region in Europe which, apart from harming human health in the region itself, poses a particular danger for wider area of southeastern Europe. Optimization of heavy metal's total emission was undertaken because years of long contamination of the soil with heavy metals of anthropogenic origin created a danger that those heavy metals may enter the food chains of animals and people, which can lead to disastrous consequences. This work represents the usage of Geographic Information System (GIS) for establishing a multifactor assessment model to quantitatively divide polluted zones and for selecting control sites in a linear programming model, combined with PROMETHEE/GAIA method, Screen View modeling system, and linear programming model. The results show that emissions at some control sites need to be cut for about 40%. In order to control the background of heavy metal pollution in Bor, the ecological environment must be improved.

  5. 78 FR 64496 - Acid Rain Program: Notice of Annual Adjustment Factors for Excess Emissions Penalty

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-10-29

    ... AGENCY Acid Rain Program: Notice of Annual Adjustment Factors for Excess Emissions Penalty AGENCY.... SUMMARY: The Acid Rain Program under title IV of the Clean Air Act provides for automatic excess emissions penalties in dollars per ton of excess emissions for sources that do not meet their annual Acid...

  6. 76 FR 71559 - Acid Rain Program: Notice of Annual Adjustment Factors for Excess Emissions Penalty

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-11-18

    ... AGENCY Acid Rain Program: Notice of Annual Adjustment Factors for Excess Emissions Penalty AGENCY.... SUMMARY: The Acid Rain Program under title IV of the Clean Air Act provides for automatic excess emissions penalties in dollars per ton of excess emissions for sources that do not meet their annual Acid...

  7. The surface energy budget and interannual variation of the annual total evaporation over a highland lake in Southwest China

    NASA Astrophysics Data System (ADS)

    Feng, Jian Wu; Liu, Hui Zhi; Sun, Ji Hua; Wang, Lei

    2015-08-01

    The turbulence spectra and energy budget were investigated based on eddy covariance method over an open-water highland lake (Erhai Lake) in Southwest China. We estimated the annual total evaporation and CO2 emission from the lake, and the evaporation trend in the past few decades was also discussed. Due to the large thermal inertia of lake water, the surface water temperature lagged behind the air temperature. Maximum lake-air temperature difference of about 4 °C had been observed in November. Water temperature profile measurements revealed that the stratification of lake water was not evident throughout the year. The spectra and cospectra of wind speed and temperature roughly satisfied the -2/3 and -4/3 rule in inertial subrange, respectively. The w spectra were observed to have a larger contribution from higher frequencies than other variables. Obvious shifts of spectra and cospectra peaks toward higher frequencies were observed as the atmospheric stratification became more stable. The lake acted as a heat sink from March through June and quickly released heat into the atmosphere from September through December. Average energy balance closure for the lake was about 80 % in 2012. The lake majorly acted as a source of CO2 to the atmosphere, but weak sinks of CO2 were observed in the summer and early fall. The total annual emission of CO2 was estimated to be 333.28 g C m-2 year-1. The annual evaporation over the lake decreased due to the increased amount of low cloud and precipitation, with the lower annual evaporation in the 1990s compared to that in the 1980s.

  8. Apparatus for Measuring Total Emissivity of Small, Low-Emissivity Samples

    NASA Technical Reports Server (NTRS)

    Tuttle, James; DiPirro, Michael J.

    2011-01-01

    An apparatus was developed for measuring total emissivity of small, lightweight, low-emissivity samples at low temperatures. The entire apparatus fits inside a small laboratory cryostat. Sample installation and removal are relatively quick, allowing for faster testing. The small chamber surrounding the sample is lined with black-painted aluminum honeycomb, which simplifies data analysis. This results in the sample viewing a very high-emissivity surface on all sides, an effect which would normally require a much larger chamber volume. The sample and chamber temperatures are individually controlled using off-the-shelf PID (proportional integral derivative) controllers, allowing flexibility in the test conditions. The chamber can be controlled at a higher temperature than the sample, allowing a direct absorptivity measurement. The lightweight sample is suspended by its heater and thermometer leads from an isothermal bar external to the chamber. The wires run out of the chamber through small holes in its corners, and the wires do not contact the chamber itself. During a steady-state measurement, the thermometer and bar are individually controlled at the same temperature, so there is zero heat flow through the wires. Thus, all of sample-temperature-control heater power is radiated to the chamber. Double-aluminized Kapton (DAK) emissivity was studied down to 10 K, which was about 25 K colder than any previously reported measurements. This verified a minimum in the emissivity at about 35 K and a rise as the temperature dropped to lower values.

  9. Continuously measured annual ammonia emissions from Southern High Plains beef cattle feedyards

    Technology Transfer Automated Retrieval System (TEKTRAN)

    The magnitude of ammonia emissions from beef cattle feedyards varies with season during the year, but studies of continuous measurement of ammonia emissions throughout the year are rare. The quantification of annual ammonia emissions will improve emission factors, provide databases that can be used ...

  10. Environmental Emissions from Energy Technology Systems: The Total Fuel Cycle

    SciTech Connect

    San Martin, Robert L.

    1989-01-01

    This is a summary report that compares emissions during the entire project life cycle for a number of fossil-fueled and renewable electric power systems, including geothermal steam (probably modeled after The Geysers). The life cycle is broken into Fuel Extraction, Construction, and Operation. The only emission covered is carbon dioxide.

  11. Environmental Emissions From Energy Technology Systems: The Total Fuel Cycle

    SciTech Connect

    San Martin, Robert L.

    1989-04-01

    This is a summary report that compares emissions during the entire project life cycle for a number of fossil-fueled and renewable electric power systems, including geothermal steam (probably modeled after The Geysers). The life cycle is broken into Fuel Extraction, Construction, and Operation. The only emission covered is carbon dioxide. (DJE 2005)

  12. Evaluation of Totally Impermeable Film for Fumigant Emissions Reduction

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Emissions from soil fumigation are stringently regulated for environmental safety concerns. Low permeability films can be used to reduce fumigant and volatile organic compound (VOC) emissions and to allow for smaller buffer zones. A large-scale field trial was conducted in Ventura, CA, to determine ...

  13. Airborne observations of aircraft aerosol emissions I: Total nonvolatile particle emission indices

    NASA Astrophysics Data System (ADS)

    Anderson, B. E.; Cofer, W. R.; Bagwell, D. R.; Barrick, J. W.; Hudgins, C. H.; Brunke, K. E.

    We report airborne measurements of total and nonvolatile (at T < 290°C) fine and ultrafine aerosol emission indices (EI's) generated by a variety of jet aircraft. The data were obtained using an instrumented jet aircraft, flown repeatedly through aircraft wakes. These aircraft were observed to produce 0.5hyphen;10 × 1015 nonvolatile particles kg-1 of fuel burned. Their numbers varied as a function of aircraft type, age, and engine operating parameters, but less with atmospheric conditions. Large numbers of volatile aerosols were measured in all cases. Volatile EI's ranged from 0.1 to 40×1016 kg-1 fuel burned. The observed soot emissions are estimated to have only a minor impact on atmospheric aerosol loading, but a future fleet producing such high concentrations of implied sulfate aerosols could perturb cloud formation and heterogeneous chemical processes in the upper troposphere/lower stratosphere.

  14. 40 CFR Appendix A to Part 72 - Methodology for Annualization of Emissions Limits

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 17 2012-07-01 2012-07-01 false Methodology for Annualization of Emissions Limits A Appendix A to Part 72 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) PERMITS REGULATION Pt. 72, App. A Appendix A to Part 72—Methodology for Annualization of Emissions Limits For...

  15. 40 CFR Appendix A to Part 72 - Methodology for Annualization of Emissions Limits

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 16 2011-07-01 2011-07-01 false Methodology for Annualization of Emissions Limits A Appendix A to Part 72 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) PERMITS REGULATION Pt. 72, App. A Appendix A to Part 72—Methodology for Annualization of Emissions Limits For...

  16. 40 CFR Appendix A to Part 72 - Methodology for Annualization of Emissions Limits

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 17 2014-07-01 2014-07-01 false Methodology for Annualization of Emissions Limits A Appendix A to Part 72 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) PERMITS REGULATION Pt. 72, App. A Appendix A to Part 72—Methodology for Annualization of Emissions Limits For...

  17. 40 CFR Appendix A to Part 72 - Methodology for Annualization of Emissions Limits

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 16 2010-07-01 2010-07-01 false Methodology for Annualization of Emissions Limits A Appendix A to Part 72 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) PERMITS REGULATION Pt. 72, App. A Appendix A to Part 72—Methodology for Annualization of Emissions Limits For...

  18. 12 CFR Appendix L to Part 226 - Assumed Loan Periods for Computations of Total Annual Loan Cost Rates

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... 12 Banks and Banking 3 2014-01-01 2014-01-01 false Assumed Loan Periods for Computations of Total Annual Loan Cost Rates L Appendix L to Part 226 Banks and Banking FEDERAL RESERVE SYSTEM (CONTINUED..., App. L Appendix L to Part 226Assumed Loan Periods for Computations of Total Annual Loan Cost Rates...

  19. 12 CFR Appendix K to Part 226 - Total Annual Loan Cost Rate Computations for Reverse Mortgage Transactions

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... 12 Banks and Banking 3 2012-01-01 2012-01-01 false Total Annual Loan Cost Rate Computations for... loan cost rate (100(.009061140 × 12))=10.87% (3) Lump sum advance at consummation and monthly advances....012 Total annual loan cost rate (100(.007708844 × 12)) = 9.25% (d) Reverse mortgage model form...

  20. 12 CFR Appendix K to Part 226 - Total Annual Loan Cost Rate Computations for Reverse Mortgage Transactions

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... 12 Banks and Banking 3 2014-01-01 2014-01-01 false Total Annual Loan Cost Rate Computations for... loan cost rate (100(.009061140 × 12))=10.87% (3) Lump sum advance at consummation and monthly advances....012 Total annual loan cost rate (100(.007708844 × 12)) = 9.25% (d) Reverse mortgage model form...

  1. A regional mass balance model based on total ammoniacal nitrogen for estimating ammonia emissions from beef cattle in Alberta Canada

    NASA Astrophysics Data System (ADS)

    Chai, Lilong; Kröbel, Roland; Janzen, H. Henry; Beauchemin, Karen A.; McGinn, Sean M.; Bittman, Shabtai; Atia, Atta; Edeogu, Ike; MacDonald, Douglas; Dong, Ruilan

    2014-08-01

    Animal feeding operations are primary contributors of anthropogenic ammonia (NH3) emissions in North America and Europe. Mathematical modeling of NH3 volatilization from each stage of livestock manure management allows comprehensive quantitative estimates of emission sources and nutrient losses. A regionally-specific mass balance model based on total ammoniacal nitrogen (TAN) content in animal manure was developed for estimating NH3 emissions from beef farming operations in western Canada. Total N excretion in urine and feces was estimated from animal diet composition, feed dry matter intake and N utilization for beef cattle categories and production stages. Mineralization of organic N, immobilization of TAN, nitrification, and denitrification of N compounds in manure, were incorporated into the model to account for quantities of TAN at each stage of manure handling. Ammonia emission factors were specified for different animal housing (feedlots, barns), grazing, manure storage (including composting and stockpiling) and land spreading (tilled and untilled land), and were modified for temperature. The model computed NH3 emissions from all beef cattle sub-classes including cows, calves, breeding bulls, steers for slaughter, and heifers for slaughter and replacement. Estimated NH3 emissions were about 1.11 × 105 Mg NH3 in Alberta in 2006, with a mean of 18.5 kg animal-1 yr-1 (15.2 kg NH3-N animal-1 yr-1) which is 23.5% of the annual N intake of beef cattle (64.7 kg animal-1 yr-1). The percentage of N intake volatilized as NH3-N was 50% for steers and heifers for slaughter, and between 11 and 14% for all other categories. Steers and heifers for slaughter were the two largest contributors (3.5 × 104 and 3.9 × 104 Mg, respectively) at 31.5 and 32.7% of total NH3 emissions because most growing animals were finished in feedlots. Animal housing and grazing contributed roughly 63% of the total NH3 emissions (feedlots, barns and pastures contributed 54.4, 0.2 and 8.1% of total emissions, respectively.). Manure storage (composting and stockpiling) and land spreading contributed 23 and 14% of the total emissions, respectively. Parameters from this TAN-based mass balance model will be incorporated into the HOLOS model - a farm-level greenhouse gas calculator.

  2. Biomass burning in Asia : annual and seasonal estimates and atmospheric emissions.

    SciTech Connect

    Streets, D. G.; Yarber, K. F.; Woo, J.-H.; Carmichael, G. R.; Decision and Information Sciences; Univ. of Iowa

    2003-10-15

    Estimates of biomass burning in Asia are developed to facilitate the modeling of Asian and global air quality. A survey of national, regional, and international publications on biomass burning is conducted to yield consensus estimates of 'typical' (i.e., non-year-specific) estimates of open burning (excluding biofuels). We conclude that 730 Tg of biomass are burned in a typical year from both anthropogenic and natural causes. Forest burning comprises 45% of the total, the burning of crop residues in the field comprises 34%, and 20% comes from the burning of grassland and savanna. China contributes 25% of the total, India 18%, Indonesia 13%, and Myanmar 8%. Regionally, forest burning in Southeast Asia dominates. National, annual totals are converted to daily and monthly estimates at 1{sup o} x 1{sup o} spatial resolution using distributions based on AVHRR fire counts for 1999--2000. Several adjustment schemes are applied to correct for the deficiencies of AVHRR data, including the use of moving averages, normalization, TOMS Aerosol Index, and masks for dust, clouds, landcover, and other fire sources. Good agreement between the national estimates of biomass burning and adjusted fire counts is obtained (R{sup 2} = 0.71--0.78). Biomass burning amounts are converted to atmospheric emissions, yielding the following estimates: 0.37 Tg of SO{sub 2}, 2.8 Tg of NO{sub x}, 1100 Tg of CO{sub 2}, 67 Tg of CO, 3.1 Tg of CH{sub 4}, 12 Tg of NMVOC, 0.45 Tg of BC, 3.3 Tg of OC, and 0.92 Tg of NH{sub 3}. Uncertainties in the emission estimates, measured as 95% confidence intervals, range from a low of {+-}65% for CO{sub 2} emissions in Japan to a high of {+-}700% for BC emissions in India.

  3. CONTINUOUS MONITORING OF TOTAL HYDROCARBON EMISSIONS FROM SLUDGE INCINERATORS

    EPA Science Inventory

    In general, the total hydrocarbon (THC) analyzers performed well. The only problems occurred when the flame failed to reignite after an automatic backpurge cycle (nine times), and on one occasion when a sample line plugged. Average THC concentration, normalized to 7% O2, was 108 ...

  4. Evaluating the effects of China's pollution control on inter-annual trends and uncertainties of atmospheric mercury emissions

    NASA Astrophysics Data System (ADS)

    Zhao, Y.; Zhong, H.; Zhang, J.; Nielsen, C. P.

    2014-10-01

    China's atmospheric mercury (Hg) emissions of anthropogenic origin have been effectively restrained through the national policy of air pollution control. Improved methods based on available field measurements are developed to quantify the benefits of Hg abatement through various emission control measures. Those measures include increased use of flue gas desulfurization (FGD) and selective catalyst reduction (SCR) systems for power sector, precalciners with fabric filter (FF) for cement production, machinery coking with electrostatic precipitator (ESP) for iron and steel production, and advanced manufacturing technologies for nonferrous metal smelting. Declining trends in emissions factors for those sources are revealed, leading to a much slower growth of national total Hg emissions than that of energy and economy, from 679 in 2005 to 750 metric tons (t) in 2012. In particular, nearly half of emissions from the above-mentioned four types of sources are expected to be reduced in 2012, attributed to expansion of technologies with high energy efficiencies and air pollutant removal rates after 2005. The speciation of Hg emissions keeps stable for recent years, with the mass fractions of around 55, 39 and 6% for Hg0, Hg2+ and Hgp, respectively. The lower estimate of Hg emissions than previous inventories is supported by limited chemistry simulation work, but middle-to-long term observation on ambient Hg levels is further needed to justify the inter-annual trends of estimated Hg emissions. With improved implementation of emission controls and energy saving, 23% reduction in annual Hg emissions for the most optimistic case in 2030 is expected compared to 2012, with total emissions below 600 t. While Hg emissions are evaluated to be gradually constrained, increased uncertainties are quantified with Monte-Carlo simulation for recent years, particularly for power and certain industrial sources. The uncertainty of Hg emissions from coal-fired power plants, as an example, increased from -48~ +73% in 2005 to -50~ +89% in 2012 (expressed as 95% confidence interval). This is attributed mainly to swiftly increased penetration of advanced manufacturing and pollutant control technologies. The unclear operation status or relatively small sample size of field measurements on those technologies results in lower but highly varied emission factors. To further confirm the benefits of pollution control polices with reduced uncertainty, therefore, systematic investigations are recommended specific for Hg pollution sources, and the variability of temporal trends and spatial distributions of Hg emissions need to be better tracked for the country under dramatic changes in economy, energy and air pollution status.

  5. 12 CFR Appendix L to Part 226 - Assumed Loan Periods for Computations of Total Annual Loan Cost Rates

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... Annual Loan Cost Rates L Appendix L to Part 226 Banks and Banking FEDERAL RESERVE SYSTEM (CONTINUED) BOARD OF GOVERNORS OF THE FEDERAL RESERVE SYSTEM TRUTH IN LENDING (REGULATION Z) Pt. 226, App. L Appendix L to Part 226Assumed Loan Periods for Computations of Total Annual Loan Cost Rates (a)...

  6. 7th Annual NASA/Contractors Conference on Quality and Productivity: "Total Quality Leadership"

    NASA Technical Reports Server (NTRS)

    1991-01-01

    More than 750 NASA, government, contractor, and academic representatives attended the Seventh Annual NASA/Contractors Conference on Quality and Productivity on October 12-13, 1990, in Grenelefe, Florida. The panel presentations and keynote speeches revolving around the theme of 'Total Quality Leadership' provided a solid base of understanding of the importance, benefits, and principles of total quality management. The implementation of these strategies is critical if we are to effectively pursue our mission of continuous quality improvement and reliability in our products, processess, and services. The annual NASA/contractors conferences serve as catalysts for achieving success in this mission. The conference was highlighted by the announcement of the first recipients of the George M. Low Trophy: NASA's Quality and Excellence Award. My congratulations go out to all nine finalist organizations and to the two recipients of this prestigious honor: Rockwell Space Systems Division and Marotta Scientific Controls, Inc. (the first small business to achieve this honor). These organizations have demonstrated a commitment to quality that is unsurpassed in the aerospace industry. This report summarizes the presentations and is not intended to be a verbatim proceedings document. You are encouraged to contact the speakers with any requests for further information.

  7. Greenhouse gas emission from the total process of swine manure composting and land application of compost

    NASA Astrophysics Data System (ADS)

    Zhong, Jia; Wei, Yuansong; Wan, Hefeng; Wu, Yulong; Zheng, Jiaxi; Han, Shenghui; Zheng, Bofu

    2013-12-01

    Greenhouse gas (GHG) emissions from animal manure management are of great concern in China. However, there are still great uncertainties about China's GHG inventory due to the GHG emission factors partly used default values from the Intergovernmental Panel of Climate Change (IPCC) guidelines. The purpose of this study was to use a case study in Beijing to determine the regional GHG emission factors based on the combination of swine manure composting and land application of the compost with both on-site examination and a life cycle assessment (LCA). The results showed that the total GHG emission factor was 240 kgCO2eq tDS-1 (dry solids), including the direct GHG emission factor of 115 kgCO2eq tDS-1 for swine manure composting and 48 kgCO2eq tDS-1 for land application of the compost. Among the total GHG emissions of 5.06 kgCH4 tDS-1 and 0.13 kgN2O tDS-1, the swine manure composting contributed approximately 89% to CH4 emissions while land application accounted for 92% of N2O emission. Meanwhile, the GHG emission profile from the full process in Beijing in 2015 and 2020 was predicted by the scenario analysis. The composting and land application is a cost-effective way for animal manure management in China considering GHG emissions.

  8. Determination of spectral and total emissivities of different new steel qualities

    NASA Astrophysics Data System (ADS)

    Bauer, Wolfgang; Rink, Matthias; Smit, Kobus

    2003-04-01

    The emissivities of different new steel grades for reactor use were determined. Numerical models for optimizing of the radiation heat transfer need total emissivities. For idealized bright metals the calculation of emissivities is possible, but not for different thermally treated surfaces. The emissivity of technical surfaces depends on numerous factors and cannot be calculated exactly based on theoretical relations. Therefore the emissivities of different pretreated steel samples have to be determined experimentally. The emissivity properties of two new steel qualities with and without different pre-treatments were investigated in the wavelength range between approx. 1.5 μm and 24 μm and the temperature range 200°C and 700°C. The results will be shown as spectral emissivities. Differences in the emissivities caused by pre-treatments will be discussed. The University of Duisburg-Essen has a measuring device for spectral emissivities. With these values temperature dependent total- and band-emissivities for use in heat transfer calculations and non-contact temperature measurements can be determined.

  9. Quantifying the contributions of natural emissions to ozone and total fine PM concentrations in the Northern Hemisphere

    NASA Astrophysics Data System (ADS)

    Zare, A.; Christensen, J. H.; Gross, A.; Irannejad, P.; Glasius, M.; Brandt, J.

    2014-03-01

    Accurate estimates of emissions from natural sources are needed for reliable predictions of ozone and fine particulate matter (PM2.5) using air quality models. In this study, the large-scale atmospheric chemistry transport model, DEHM (the Danish Eulerian Hemispheric Model) is further developed, evaluated and applied to study and quantify the contributions of natural emissions of VOCs, NOx, NH3, SO2, CH4, PM, CO and sea salt to the concentration of ozone and formation of PM2.5 for the year 2006. Natural source categories adopted in the recent model are vegetation, lightning, soils, wild animals and oceans. In this study, the model has been further developed to include more Biogenic Volatile Organic Compounds (BVOCs) and to implement a scheme for secondary organic aerosols as well as an updated description of sea-salt emissions. Our simulations indicate that in the Northern Hemisphere the contribution from natural emissions to the average annual ozone mixing ratios over land is between 4-30 ppbV. Among the natural emissions, BVOCs are found to be the most significant contributors to ozone formation in 2006, enhancing the average ozone mixing ratio by about 11% over the land areas of the Northern Hemisphere. The relative contribution of all the natural emissions to ozone is found to be highest in the northern part of South America by about 42%. Similarly, the highest contribution of all the natural sources to total fine particles over land is found to be in South America by about 74% and sea-salt aerosols demonstrated to play the most important role. However, over the rest of the regions in the model domain the largest contribution from the natural sources to PM2.5 in the specific year 2006 is due to wildfires. The contribution from natural emissions to the mean PM2.5 concentration over the land areas in the model domain is about 34%.

  10. Quantifying the contributions of natural emissions to ozone and total fine PM concentrations in the Northern Hemisphere

    NASA Astrophysics Data System (ADS)

    Zare, A.; Christensen, J. H.; Gross, A.; Irannejad, P.; Glasius, M.; Brandt, J.

    2013-06-01

    Accurate estimates of emissions from natural sources are needed for reliable predictions of ozone and fine particulate matter (PM2.5) using air quality models. In this study, the large-scale atmospheric chemistry transport model, DEHM (the Danish Eulerian Hemispheric Model) is further developed, evaluated and applied to study and quantify the contributions of natural emissions of VOCs, NOx, NH3, SO2, CH4, PM, CO and sea salt to the concentration of ozone and formation of PM2.5 for the year 2006. Natural source categories adopted in the recent model are vegetation, lightning, soils, wild animals and oceans. In this study, the model has been further developed to include more biogenic volatile organic compounds (BVOCs) and to implement a scheme for secondary organic aerosol as well as an updated description of sea-salt emissions. Our simulations indicate that at Northern Hemisphere the contribution from natural emissions to the average annual ozone concentrations over land is between 4-30 ppbV. Among the natural emissions, BVOCs are found to be the most significant contributors to ozone formation, enhancing the average ozone concentration by about 11% over the land areas of the Northern Hemisphere. The relative contribution of all the natural emissions to ozone is found to be highest in the northern part of South America by about 42%. Similarly, the highest contribution of all the natural sources to total fine particles over land is found to be in South America by about 74% and sea-salt aerosols demonstrated to play the most important role. However, over the rest of regions in the model domain the largest contribution from the natural sources to PM2.5 is due to wildfires. The contribution from natural emissions to the mean PM2.5 concentration over the land areas in the model domain is about 34%.

  11. Evaluating the effects of China's pollution controls on inter-annual trends and uncertainties of atmospheric mercury emissions

    NASA Astrophysics Data System (ADS)

    Zhao, Y.; Zhong, H.; Zhang, J.; Nielsen, C. P.

    2015-04-01

    China's anthropogenic emissions of atmospheric mercury (Hg) are effectively constrained by national air pollution control and energy efficiency policies. In this study, improved methods, based on available data from domestic field measurements, are developed to quantify the benefits of Hg abatement by various emission control measures. Those measures include increased use of (1) flue gas desulfurization (FGD) and selective catalyst reduction (SCR) systems in power generation; (2) precalciner kilns with fabric filters (FF) in cement production; (3) mechanized coking ovens with electrostatic precipitators (ESP) in iron and steel production; and (4) advanced production technologies in nonferrous metal smelting. Investigation reveals declining trends in emission factors for each of these sources, which together drive a much slower growth of total Hg emissions than the growth of China's energy consumption and economy, from 679 metric tons (t) in 2005 to 750 t in 2012. In particular, estimated emissions from the above-mentioned four source types declined 3% from 2005 to 2012, which can be attributed to expanded deployment of technologies with higher energy efficiencies and air pollutant removal rates. Emissions from other anthropogenic sources are estimated to increase by 22% during the period. The species shares of total Hg emissions have been stable in recent years, with mass fractions of around 55, 39, and 6% for gaseous elemental Hg (Hg0), reactive gaseous mercury (Hg2+), and particle-bound mercury (Hgp), respectively. The higher estimate of total Hg emissions than previous inventories is supported by limited simulation of atmospheric chemistry and transport. With improved implementation of emission controls and energy saving, a 23% reduction in annual Hg emissions from 2012 to 2030, to below 600 t, is expected at the most. While growth in Hg emissions has been gradually constrained, uncertainties quantified by Monte Carlo simulation for recent years have increased, particularly for the power sector and particular industrial sources. The uncertainty (expressed as 95% confidence intervals) of Hg emissions from coal-fired power plants, for example, increased from -48-+73% in 2005 to -50-+89% in 2012. This is attributed mainly to increased penetration of advanced manufacturing and pollutant control technologies; the unclear operational status and relatively small sample sizes of field measurements of those processes have resulted in lower but highly varied emission factors. To reduce uncertainty and further confirm the benefits of pollution control and energy polices, therefore, systematic investigation of specific Hg pollution sources is recommended. The variability of temporal trends and spatial distributions of Hg emissions needs to be better tracked during the ongoing dramatic changes in China's economy, energy use, and air pollution status.

  12. Longitudinal dependence of annual cycle of total ozone in the Northern mid-latitudes

    NASA Astrophysics Data System (ADS)

    Milinevsky, Gennadi; Evtushevsky, Oleksandr; Grytsai, Asen

    2015-04-01

    In the Northern mid-latitudes, annual change of the total ozone content (TOC) in terms of zonal means is mainly determined by stratospheric ozone accumulation in winter and spring due to the Brewer-Dobson circulation (BDC) and following photochemical relaxation continuing to autumn. It is known from previous studies that annual TOC cycle in some regions could be close to or differ from the zonal mean one. For example, annual TOC minimum over Eastern Asia is observed two months earlier (August) than over Europe (October). In this work, a consecutive analysis of the TOC seasonality along the latitudinal belt 50-55°N in 36 segments (10°-step in longitude) is analyzed. The latitude range includes northern Ukraine and Kyiv-Goloseyev Dobson station. Analysis is based on the Merged Ozone Data Set (MOD) reanalysis 1979-2011 (http://acd-ext.gsfc.nasa.gov/Data_services/merged/). We use also the NCEP-NCAR reanalysis data (http://www.esrl.noaa.gov/psd/cgi-bin/data/composites/printpage.pl) to estimate seasonal changes in geopotential heights and tropopause heights. It is shown that the seasonal TOC cycle over the cyclonic anomalies (high mean TOC level) is shifted to the beginning of year in comparison with that over the anticyclonic anomalies (low mean TOC level). The largest TOC values over the Aleutian low (around 150°E) are characterized by the earliest seasonal maximum (February-March) and minimum (August). Here, the tropospheric dynamics (winter/summer extremes in the planetary wave activity and stationary pressure anomaly formation/disappearance) and related tropopause effects seem to have dominant influence on the earliest development of the annual TOC cycle. Zonal asymmetry in stratospheric ozone accumulation influences rather the maximum TOC levels in this region than timing of the TOC extremes. In the opposite longitude range (zonal TOC minimum in region of the Azores high influence, 20-30°W), the annual TOC cycle lags by 2-3 months reaching a TOC maximum in May and a TOC minimum in November. Seasonal changes in this subtropical anomaly (pressure and tropopause height) are weak. Hence, troposphere influence on the TOC seasonality here is small in comparison with Aleutian low region. Slow accumulation of the stratospheric ozone during winter and spring leads to the latest occurrence of seasonal TOC maximum. Photochemical ozone relaxation lasts also longer up to beginning of the next BDC intensification since December. The results of this analysis could be useful for explanation of the interannual variations in the local annual TOC cycles considering the climatological ones in neighboring segments of the northern midlatitudes. Possible effects of the TOC seasonality in regional climate changes could also be analyzed in future studies. Acknowledgments. This work was partly supported by the Polar FORCeS project no. 4012 of the Australian Antarctic Science Program.

  13. 500 years of mercury production: global annual inventory by region until 2000 and associated emissions.

    PubMed

    Hylander, Lars D; Meili, Markus

    2003-03-20

    Since pre-industrial times, anthropogenic emissions of Hg have at least doubled global atmospheric Hg deposition rates. In order to minimize environmental and human health effects, efforts have been made to reduce Hg emissions from industries and power plants, while less attention has been paid to Hg mining. This paper is a compilation of available data on primary Hg production and associated emissions with regional and annual resolution since colonial times. Globally, approximately one million tons of metallic Hg has been extracted from cinnabar and other ores during the past five centuries, half already before 1925. Roughly half has been used for mining of gold and silver, but the annual Hg production peaked during a short period of recent industrial uses. Comparison with total historic Hg deposition from global anthropogenic emissions (0.1-0.2 Mtons) suggests that only a few percent of all mined Hg have escaped to the atmosphere thus far. While production of primary Hg has changed dramatically over time and among mines, the global production has always been dominant in the region of the mercuriferous belt between the western Mediterranean and central Asia, but appears to be shifting to the east. Roughly half of the registered Hg has been extracted in Europe, where Spanish mines alone have contributed one third of the world's mined Hg. Approximately one fourth has been mined in the Americas, and most of the remaining registered Hg in Asia. However, the Asian figures may be largely underestimated. Presently, the dominant Hg mines are in Almadén in Spain (236 t of Hg produced in 2000), Khaydarkan in Kyrgyzstan (550 t), Algeria (estimated 240 t) and China (ca. 200 t). Mercury by-production from mining of other metals (e.g. copper, zinc, gold, silver) in 2000 includes 48 t from Peru, 45 t from Finland and at least 15 t from the USA. Since 1970, the recorded production of primary Hg has been reduced by almost an order of magnitude to approximately 2000 t in the year 2000. Mining is thus still of similar magnitude as all current anthropogenic Hg emissions to the atmosphere, and mined Hg may account for more than one third of these emissions. Also before use, mercury is emitted from Hg mines locally during the mining and refining processes and from mining waste. Global direct emissions to the atmosphere amount to 10-30 t per year currently (up to 10 at Almadén alone), and probably exceed 10000 t historically. Termination of Hg mining will reduce associated local emissions to the atmosphere and biosphere. Since several economically viable Hg-free alternatives exist for practically all applications of Hg, the production and use of Hg can be further reduced and all primary production of Hg other than by-production terminated. PMID:12663168

  14. Radionuclide air emissions annual report for calendar year 1994

    SciTech Connect

    Not Available

    1995-04-04

    This report presents the results of the Pinellas Plant air sampling program for the year of 1994. Topics discussed include: site description; source description; air emissions data; dose assessments; description of dose model; summary of input parameters of dose model; unplanned releases; and diffuse emissions. Included in the attachments of this document are: non-radon individual dose assessment; non-radon population dose assessment; summary of stack flow rate measurements; HOTSPOT computer model run; and meteorological data for the Pinellas Plant for 1994.

  15. Radionuclide air emissions. Annual report for calendar year 1997

    SciTech Connect

    1997-08-01

    A description is provided of radioactive effluent releases from the Pinellas Plant. The DOE sold the Pinellas Plant in March 1995. A portion of the plant was backed by DOE until September 1997 to facilitate a safe transition to commercial ventures.The plant`s radiological processing equipment was cleaned from past DOE operations. Emissions from the cleanup activity were monitored.

  16. Annual Carbon Emissions from Deforestation in the Amazon Basin between 2000 and 2010.

    PubMed

    Song, Xiao-Peng; Huang, Chengquan; Saatchi, Sassan S; Hansen, Matthew C; Townshend, John R

    2015-01-01

    Reducing emissions from deforestation and forest degradation (REDD+) is considered one of the most cost-effective strategies for mitigating climate change. However, historical deforestation and emission rates-critical inputs for setting reference emission levels for REDD+-are poorly understood. Here we use multi-source, time-series satellite data to quantify carbon emissions from deforestation in the Amazon basin on a year-to-year basis between 2000 and 2010. We first derive annual deforestation indicators by using the Moderate Resolution Imaging Spectroradiometer Vegetation Continuous Fields (MODIS VCF) product. MODIS indicators are calibrated by using a large sample of Landsat data to generate accurate deforestation rates, which are subsequently combined with a spatially explicit biomass dataset to calculate committed annual carbon emissions. Across the study area, the average deforestation and associated carbon emissions were estimated to be 1.59 ± 0.25 M ha•yr(-1) and 0.18 ± 0.07 Pg C•yr(-1) respectively, with substantially different trends and inter-annual variability in different regions. Deforestation in the Brazilian Amazon increased between 2001 and 2004 and declined substantially afterwards, whereas deforestation in the Bolivian Amazon, the Colombian Amazon, and the Peruvian Amazon increased over the study period. The average carbon density of lost forests after 2005 was 130 Mg C•ha(-1), ~11% lower than the average carbon density of remaining forests in year 2010 (144 Mg C•ha(-1)). Moreover, the average carbon density of cleared forests increased at a rate of 7 Mg C•ha(-1)•yr(-1) from 2005 to 2010, suggesting that deforestation has been progressively encroaching into high-biomass lands in the Amazon basin. Spatially explicit, annual deforestation and emission estimates like the ones derived in this study are useful for setting baselines for REDD+ and other emission mitigation programs, and for evaluating the performance of such efforts. PMID:25951328

  17. Annual Carbon Emissions from Deforestation in the Amazon Basin between 2000 and 2010

    PubMed Central

    Song, Xiao-Peng; Huang, Chengquan; Saatchi, Sassan S.; Hansen, Matthew C.; Townshend, John R.

    2015-01-01

    Reducing emissions from deforestation and forest degradation (REDD+) is considered one of the most cost-effective strategies for mitigating climate change. However, historical deforestation and emission rates―critical inputs for setting reference emission levels for REDD+―are poorly understood. Here we use multi-source, time-series satellite data to quantify carbon emissions from deforestation in the Amazon basin on a year-to-year basis between 2000 and 2010. We first derive annual deforestation indicators by using the Moderate Resolution Imaging Spectroradiometer Vegetation Continuous Fields (MODIS VCF) product. MODIS indicators are calibrated by using a large sample of Landsat data to generate accurate deforestation rates, which are subsequently combined with a spatially explicit biomass dataset to calculate committed annual carbon emissions. Across the study area, the average deforestation and associated carbon emissions were estimated to be 1.59 ± 0.25 M ha•yr−1 and 0.18 ± 0.07 Pg C•yr−1 respectively, with substantially different trends and inter-annual variability in different regions. Deforestation in the Brazilian Amazon increased between 2001 and 2004 and declined substantially afterwards, whereas deforestation in the Bolivian Amazon, the Colombian Amazon, and the Peruvian Amazon increased over the study period. The average carbon density of lost forests after 2005 was 130 Mg C•ha−1, ~11% lower than the average carbon density of remaining forests in year 2010 (144 Mg C•ha−1). Moreover, the average carbon density of cleared forests increased at a rate of 7 Mg C•ha−1•yr−1 from 2005 to 2010, suggesting that deforestation has been progressively encroaching into high-biomass lands in the Amazon basin. Spatially explicit, annual deforestation and emission estimates like the ones derived in this study are useful for setting baselines for REDD+ and other emission mitigation programs, and for evaluating the performance of such efforts. PMID:25951328

  18. Measurements of Total Hemispherical Emissivity of Several Stably Oxidized Metals and Some Refractory Oxide Coatings

    NASA Technical Reports Server (NTRS)

    Wade, William R.

    1959-01-01

    A description of the apparatus and methods used for obtaining total hemispherical emissivity is presented, and data for several stably oxidized metals are included. The metals which were tested included type 347 stainless steel, tungsten, and Haynes alloys B, C, X, and 25. No values of emissivity were obtained for tungsten or Haynes alloy B because of the nature of the oxides produced. The refractory oxide coatings tested were flame-sprayed alumina and zirconia. The results of the investigation indicate that strongly adherent, oxidized surfaces of a high stable emissivity can be produced on type 347 stainless steel for which the total hemispherical emissivity varied from 0.87 to 0.91 for temperatures from 600 F to 2,000 F. For this same temperature range, the Haynes alloys tested showed values of total hemispherical emissivity from 0.90 to 0.96 for alloy C, from 0.85 to 0.88 for alloy X, and from 0.85 to 0.89 for alloy 25. Haynes alloy B and tungsten formed nonadherent oxides at elevated temperatures and, therefore, stable emissivities were not obtained. The results obtained for the flame-sprayed ceramics (alumina and zirconia) showed considerably higher values of total emissivity than those measured for coatings applied by other methods. Emissivity values ranging from 0.69 to 0.44 for aluminum oxide and from 0.62 to 0.44 for zirconium oxide were measured for temperatures from 800 F to 2,000 F.

  19. Energy use and emissions from marine vessels: a total fuel life cycle approach.

    PubMed

    Winebrake, James J; Corbett, James J; Meyer, Patrick E

    2007-01-01

    Regional and global air pollution from marine transportation is a growing concern. In discerning the sources of such pollution, researchers have become interested in tracking where along the total fuel life cycle these emissions occur. In addition, new efforts to introduce alternative fuels in marine vessels have raised questions about the energy use and environmental impacts of such fuels. To address these issues, this paper presents the Total Energy and Emissions Analysis for Marine Systems (TEAMS) model. TEAMS can be used to analyze total fuel life cycle emissions and energy use from marine vessels. TEAMS captures "well-to-hull" emissions, that is, emissions along the entire fuel pathway, including extraction, processing, distribution, and use in vessels. TEAMS conducts analyses for six fuel pathways: (1) petroleum to residual oil, (2) petroleum to conventional diesel, (3) petroleum to low-sulfur diesel, (4) natural gas to compressed natural gas, (5) natural gas to Fischer-Tropsch diesel, and (6) soybeans to biodiesel. TEAMS calculates total fuel-cycle emissions of three greenhouse gases (carbon dioxide, nitrous oxide, and methane) and five criteria pollutants (volatile organic compounds, carbon monoxide, nitrogen oxides, particulate matter with aerodynamic diameters of 10 microm or less, and sulfur oxides). TEAMS also calculates total energy consumption, fossil fuel consumption, and petroleum consumption associated with each of its six fuel cycles. TEAMS can be used to study emissions from a variety of user-defined vessels. This paper presents TEAMS and provides example modeling results for three case studies using alternative fuels: a passenger ferry, a tanker vessel, and a container ship. PMID:17269235

  20. Unidirectional total variation destriping using difference curvature in MODIS emissive bands

    NASA Astrophysics Data System (ADS)

    Wang, Mi; Zheng, Xinghui; Pan, Jun; Wang, Bin

    2016-03-01

    This paper presents a method of unidirectional total variation destriping using difference curvature in MODIS (Moderate Resolution Imaging Spectrometer) emissive bands. First, difference curvature is utilized to extract spatial information at each pixel; and the spatially weighted parameters that constructed by extracted spatial information are incorporated into the unidirectional total variation model to adaptively adjust the destriping strength for achieving a better destriping result and preserving the detail information meantime. Second, the split Bregman iteration method is employed to optimize the proposed model. Finally, experimental results from MODIS emissive bands and comparisons with other methods demonstrate the potential of the presented method for MODIS image destriping.

  1. Summary Report of the Seventh Annual NASA/Contractors Conference on Quality and Productivity: "Total Quality Leadership"

    NASA Technical Reports Server (NTRS)

    1991-01-01

    More than 750 NASA, government, contractor, and academic representatives attended the Seventh Annual NASA/Contractors Conference on Quality and Productivity on October 12-13, 1990, in Grenelefe, Florida. The panel presentations and keynote speeches revolving around the theme of 'Total Quality Leadership" provided a solid base of understanding of the importance, benefits, and principles of total quality management. The implementation of these strategies is critical if we are to effectively pursue our mission of continuous quality improvement and reliability in our products, processes, and services. The annual NASA/contractors conferences serve as catalysts for achieving success in this mission.

  2. 40 CFR Appendix A to Part 72 - Methodology for Annualization of Emissions Limits

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 17 2013-07-01 2013-07-01 false Methodology for Annualization of Emissions Limits A Appendix A to Part 72 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) PERMITS REGULATION Pt. 72, App. A Appendix A to Part 72—Methodology...

  3. 40 CFR 63.1431 - Process vent annual epoxides emission factor plan requirements.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... factor plan requirements. 63.1431 Section 63.1431 Protection of Environment ENVIRONMENTAL PROTECTION... group determination procedures in the NESHAP for Group I Polymers and Resins (40 CFR part 63, subpart U... Production § 63.1431 Process vent annual epoxides emission factor plan requirements. (a) Applicability...

  4. Spectral and total temperature-dependent emissivities of few-layer structures on a metallic substrate.

    PubMed

    Blandre, Etienne; Chapuis, Pierre-Olivier; Vaillon, Rodolphe

    2016-01-25

    We investigate the thermal radiative emission of few-layer structures deposited on a metallic substrate and its dependence on temperature with the Fluctuational Electrodynamics approach. We highlight the impact of the variations of the optical properties of metallic layers on their temperature-dependent emissivity. Fabry-Pérot spectral selection involving at most two transparent layers and one thin reflective layer leads to well-defined peaks and to the amplification of the substrate emission. For a single Fabry-Pérot layer on a reflective substrate, an optimal thickness that maximizes the emissivity of the structure can be determined at each temperature. A thin lossy layer deposited on the previous structure can enhance interference phenomena, and the analysis of the participation of each layer to the emission shows that the thin layer is the main source of emission. Eventually, we investigate a system with two Fabry-Pérot layers and a metallic thin layer, and we show that an optimal architecture can be found. The total hemispherical emissivity can be increased by one order of magnitude compared to the substrate emissivity. PMID:26832589

  5. Greenhouse gas emissions of drained fen peatlands in Belarus are controlled by water table, land use, and annual weather conditions

    NASA Astrophysics Data System (ADS)

    Burlo, Andrei; Minke, Merten; Chuvashova, Hanna; Augustin, Jürgen; Hoffmann, Mathias; Narkevitch, Ivan

    2014-05-01

    Drainage of peatlands causes strong emission of the greenhouse gases (GHG) CO2 and N2O, sometimes combined with a weak CH4 uptake. In Belarus drained peatlands occupy about 1505000 ha or more than 7.2 % of the country area. Joosten (2009) estimates CO2 emission from degraded peatlands in Belarus as 41.3 Mt yr-1 what equals to 47 % of total anthropogenic greenhouse gases (GHGs) emission of country in 2011. However, it could not be checked if these numbers are correct since there are no GHG measurements on these sites up to now. Therefore we studied the GHG emissions with the closed chamber approach in four peatlands situated in central and southern Belarus over a period from August 2010 to August 2012. The measurements comprised eight site types representing different water level conditions, and ranging from grassland and arable land over abandoned fields and peat cuts to near-natural sedge fens. Fluxes of CH4 and N2O were determined using the close-chamber approach every second week in snow free periods and every fourth week during winter time. The annual emissions were calculated based on linear interpolation. Carbon dioxide exchange was measured with transparent and opaque chambers every 3-4 weeks and the annual net ecosystem exchange (NEE) was modeled according to Drösler (2005). Most of the drained sites were sources of CO2 in both years. NEE increased with lower mean annual water table level. The highest NEE value (1263.5 g CO2-C m-1yr-1) was observed at the driest site of the study; an abandoned fen formerly used for agriculture. In contrast, a former peat extraction site with moist peat and small Pinus sylvestris tress were sinks of CO2 with uptake to 389.6 g CO2-C m-1yr-1. The highest N2O emissions were recorded at a drained agricultural fen with mean annual rates of up to 2347 mg N2O-N m-2 yr-1. Significant fluxes of CH4 (15 g CH4C m-2 h-1) were observed only at the near-natural site in the first year of investigation when precipitation and the mean water level were high. At the drained sites fluxes of CH4 were mainly close to null and sometimes a weak uptake of CH4 (-0.06 mg CH4-C m-2 h-1) was observed. In general the results show an increase of global warming potential of site with decreasing mean annual water level from 5.5 t CO2 equivalents ha-1yr-1 at near-natural site with annual mean water level -8 cm to 51 t CO2 equivalents ha-1yr-1 at abandoned fen formerly used for agriculture with mean annual water level near -90 cm. This study was conducted in the framework of the BMU financed project 'Restoring Peatlands and applying Concepts for Sustainable Management in Belarus - Climate Change Mitigation with Economic and Biodiversity Benefits'. Joosten H. The Global Peatland CO2 Picture: peatland status and drainage related emissions in all countries of the world - 2009.

  6. Particle size distribution characteristics of cotton gin mote trash system total particulate emissions

    Technology Transfer Automated Retrieval System (TEKTRAN)

    This report is part of a project to characterize cotton gin emissions from the standpoint of total particulate stack sampling and particle size analyses. In 2013, EPA published a more stringent standard for particulate matter with nominal diameter less than or equal to 2.5 µm (PM2.5). This created a...

  7. Particle size distribution characteristics of cotton gin battery condenser system total particulate emissions

    Technology Transfer Automated Retrieval System (TEKTRAN)

    This report is part of a project to characterize cotton gin emissions from the standpoint of total particulate stack sampling and particle size analyses. In 2013, EPA published a more stringent standard for particulate matter with nominal diameter less than or equal to 2.5 µm (PM2.5). This created a...

  8. Particle size distribution characteristics of cotton gin master trash system total particulate emissions

    Technology Transfer Automated Retrieval System (TEKTRAN)

    This report is part of a project to characterize cotton gin emissions from the standpoint of total particulate stack sampling and particle size analyses. In 2013, EPA published a more stringent standard for particulate matter with nominal diameter less than or equal to 2.5 µm (PM2.5). This created a...

  9. Particle size distribution characteristics of cotton gin mote cleaner system total particulate emissions

    Technology Transfer Automated Retrieval System (TEKTRAN)

    This report is part of a project to characterize cotton gin emissions from the standpoint of total particulate stack sampling and particle size analyses. In 2013, EPA published a more stringent standard for particulate matter with nominal diameter less than or equal to 2.5 µm (PM2.5). This created a...

  10. Particle size distribution characteristics of cotton gin combined lint cleaning system total particulate emissions

    Technology Transfer Automated Retrieval System (TEKTRAN)

    This report is part of a project to characterize cotton gin emissions from the standpoint of total particulate stack sampling and particle size analyses. In 2013, EPA published a more stringent standard for particulate matter with nominal diameter less than or equal to 2.5 µm (PM2.5). This created a...

  11. Particle size distribution characteristics of cotton gin mote cyclone robber system total particulate emissions

    Technology Transfer Automated Retrieval System (TEKTRAN)

    This report is part of a project to characterize cotton gin emissions from the standpoint of total particulate stack sampling and particle size analyses. In 2013, EPA published a more stringent standard for particulate matter with nominal diameter less than or equal to 2.5 µm (PM2.5). This created a...

  12. TOTAL PARTICLE, SULFATE, AND ACIDIC AEROSOL EMISSIONS FROM KEROSENE SPACE HEATERS

    EPA Science Inventory

    Chamber studies were conducted on four unvented kerosene space heaters to assess emissions of total particle, sulfate, and acidic aerosol. The heaters tested represented four burner designs currently in use by the public. Kerosene space heaters are a potential source of fine part...

  13. Novel Sampling Techniques for Measurement of Turbine Engine Total Particulate Matter Emissions

    EPA Science Inventory

    This is the first progress report of a study to evaluate two different condensation devices for the measurement of the total (volatile + non-volatile) particulate matter (PM) emissions from aircraft turbine engines by direct sampling at the engine exit. The characteristics of th...

  14. Particle size distribution characteristics of cotton gin overflow system total particulate emissions

    Technology Transfer Automated Retrieval System (TEKTRAN)

    This report is part of a project to characterize cotton gin emissions from the standpoint of total particulate stack sampling and particle size analyses. In 2013, EPA published a more stringent standard for particulate matter with nominal diameter less than or equal to 2.5 µm (PM2.5). This created a...

  15. Particle size distribution characteristics of cotton gin second stage mote system total particulate emissions

    Technology Transfer Automated Retrieval System (TEKTRAN)

    This report is part of a project to characterize cotton gin emissions from the standpoint of total particulate stack sampling and particle size analyses. In 2013, EPA published a more stringent standard for particulate matter with nominal diameter less than or equal to 2.5 µm (PM2.5). This created a...

  16. Particle size distribution characteristics of cotton gin combined mote system total particulate emissions

    Technology Transfer Automated Retrieval System (TEKTRAN)

    This report is part of a project to characterize cotton gin emissions from the standpoint of total particulate stack sampling and particle size analyses. In 2013, EPA published a more stringent standard for particulate matter with nominal diameter less than or equal to 2.5 µm (PM2.5). This created a...

  17. AUTOMATIC INTERFACING SYSTEM FOR SAMPLING TOTAL MERCURY IN STATIONARY SOURCE EMISSIONS

    EPA Science Inventory

    An interfacing system to sample total mercury emissions in source streams and suitably condition, dilute, and transport the sample to a mercury measuring instrument was designed, fabricated, and tested. The system consists of three components: a conditioner, a diluter, and a pump...

  18. Correlating benzene, total hydrocarbon and carbon monoxide emissions from wood-fired boilers

    SciTech Connect

    Hubbard, A.J.; Grande, D.E.; Berens, J.R.; Piotrowski, J.

    1997-12-31

    Hazardous air pollutants, including benzene, are generated by the incomplete combustion of fuels. Organic compound emissions, which are generally products of incomplete combustion, are reduced by promoting high quality combustion, for example by controlling furnace exit temperatures and establishing minimum residence times. Monitoring carbon monoxide (CO) emissions is important since the amount of carbon monoxide emitted represents the quality of combustion which in turn represents the amount of hazardous air pollutants being generated. Total hydrocarbon (THC) emissions are also related to the quality of combustion. Recently the Wisconsin Department of Natural Resources (DNR) measured the benzene and total hydrocarbon emissions from two large industrial wood fired boilers. These boilers are located at Tenneco Packaging, a container board manufacturing facility in northern Wisconsin. Temperature, oxygen and carbon monoxide concentrations were sampled continuously by Tenneco Packaging`s emission monitoring system. The Department`s team used an organic vapor analyzer to continuously measure concentrations of total hydrocarbons (THC). The Department`s team also used a modified USEPA Method 18 sampling train to capture organic vapors for subsequent analysis by gas chromatography. The data show correlations between benzene and carbon monoxide, and between benzene and THC concentrations. The emissions sampling occurred both upstream of the particulate emissions control system as well as at the stack. The CO variations during actual boiler operation appeared to be well correlated with changes in boiler steam load. That is, increases in CO generally accompanied a change, either up or down, in boiler load. Lower concentrations of CO were associated with stable combustion, as indicated by periods of constant or nearly constant boiler load.

  19. Consumption-based Total Suspended Particulate Matter Emissions in Jing-Jin-Ji Area of China

    NASA Astrophysics Data System (ADS)

    Yang, S.; Chen, S.; Chen, B.

    2014-12-01

    The highly-industrialized regions in China have been facing a serious problem of haze mainly consisted of total suspended particulate matter (TSPM), which has attracted great attention from the public since it directly impairs human health and clinically increases the risks of various respiratory and pulmonary diseases. In this paper, we set up a multi-regional input-output (MRIO) model to analyze the transferring routes of TSPM emissions between regions through trades. TSPM emission from particulate source regions and sectors are identified by analyzing the embodied TSPM flows through monetary flow and carbon footprint. The track of TSPM from origin to end via consumption activities are also revealed by tracing the product supply chain associated with the TSPM emissions. Beijing-Tianjin-Hebei (Jing-Jin-Ji) as the most industrialized area of China is selected for a case study. The result shows that over 70% of TSPM emissions associated with goods consumed in Beijing and Tianjin occurred outside of their own administrative boundaries, implying that Beijing and Tianjin are net embodied TSPM importers. Meanwhile, 63% of the total TSPM emissions in Hebei Province are resulted from the outside demand, indicating Hebei is a net exporter. In addition, nearly half of TSPM emissions are the by-products related to electricity and heating supply and non-metal mineral products in Jing-Jin-Ji Area. Based on the model results, we provided new insights into establishing systemic strategies and identifying mitigation priorities to stem TSPM emissions in China. Keywords: total suspended particulate matter (TSPM); urban ecosystem modeling; multi-regional input-output (MRIO); China

  20. The total hemispheric emissivity of painted aluminum honeycomb at cryogenic temperatures

    SciTech Connect

    Tuttle, J.; Canavan, E.; DiPirro, M.; Li, X.; Knollenberg, P.

    2014-01-29

    NASA uses high-emissivity surfaces on deep-space radiators and thermal radiation absorbers in test chambers. Aluminum honeycomb core material, when coated with a high-emissivity paint, provides a lightweight, mechanically robust, and relatively inexpensive black surface that retains its high emissivity down to low temperatures. At temperatures below about 100 Kelvin, this material performs much better than the paint itself. We measured the total hemispheric emissivity of various painted honeycomb configurations using an adaptation of an innovative technique developed for characterizing thin black coatings. These measurements were performed from room temperature down to 30 Kelvin. We describe the measurement technique and compare the results with predictions from a detailed thermal model of each honeycomb configuration.

  1. 76 FR 3142 - Notice of Annual Adjustment of the Cap on Average Total Assets That Defines Community Financial...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-01-19

    ... 75 FR 9601 (Mar. 3, 2010). II. The CFI Asset Cap for 2011 As of January 1, 2011, FHFA has increased... From the Federal Register Online via the Government Publishing Office FEDERAL HOUSING FINANCE AGENCY Notice of Annual Adjustment of the Cap on Average Total Assets That Defines Community...

  2. 75 FR 9601 - Notice of Annual Adjustment of the Cap on Average Total Assets That Defines Community Financial...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-03-03

    .... Accordingly, as of January 1, 2009, the adjusted CFI asset cap was $1,011,000,000. See 74 FR 7438 (Feb. 17... From the Federal Register Online via the Government Publishing Office FEDERAL HOUSING FINANCE AGENCY Notice of Annual Adjustment of the Cap on Average Total Assets That Defines Community...

  3. 77 FR 14366 - Notice of Annual Adjustment of the Cap on Average Total Assets That Defines Community Financial...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-03-09

    ... stated that the cap had been set at $1,040,000,000. See 76 FR 3142 (Jan. 19, 2011). \\1\\ See 12 U.S.C... From the Federal Register Online via the Government Publishing Office FEDERAL HOUSING FINANCE AGENCY Notice of Annual Adjustment of the Cap on Average Total Assets That Defines Community...

  4. 12 CFR Appendix L to Part 226 - Assumed Loan Periods for Computations of Total Annual Loan Cost Rates

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... borrower to become obligated on the reverse mortgage loan, as shown in the U.S. Decennial Life Tables for... 12 Banks and Banking 3 2010-01-01 2010-01-01 false Assumed Loan Periods for Computations of Total Annual Loan Cost Rates L Appendix L to Part 226 Banks and Banking FEDERAL RESERVE SYSTEM...

  5. 12 CFR Appendix L to Part 1026 - Assumed Loan Periods for Computations of Total Annual Loan Cost Rates

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 12 Banks and Banking 8 2013-01-01 2013-01-01 false Assumed Loan Periods for Computations of Total Annual Loan Cost Rates L Appendix L to Part 1026 Banks and Banking BUREAU OF CONSUMER FINANCIAL PROTECTION TRUTH IN LENDING (REGULATION Z) Pt. 1026, App. L Appendix L to Part 1026Assumed Loan Periods...

  6. 12 CFR Appendix L to Part 1026 - Assumed Loan Periods for Computations of Total Annual Loan Cost Rates

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... 12 Banks and Banking 8 2012-01-01 2012-01-01 false Assumed Loan Periods for Computations of Total Annual Loan Cost Rates L Appendix L to Part 1026 Banks and Banking BUREAU OF CONSUMER FINANCIAL PROTECTION TRUTH IN LENDING (REGULATION Z) Pt. 1026, App. L Appendix L to Part 1026Assumed Loan Periods...

  7. 12 CFR Appendix K to Part 1026 - Total Annual Loan Cost Rate Computations for Reverse Mortgage Transactions

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... 12 Banks and Banking 8 2012-01-01 2012-01-01 false Total Annual Loan Cost Rate Computations for Reverse Mortgage Transactions K Appendix K to Part 1026 Banks and Banking BUREAU OF CONSUMER FINANCIAL... transactions, as well as instructions, explanations, and examples for various transactions. This appendix...

  8. 12 CFR Appendix K to Part 1026 - Total Annual Loan Cost Rate Computations for Reverse Mortgage Transactions

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 12 Banks and Banking 8 2013-01-01 2013-01-01 false Total Annual Loan Cost Rate Computations for Reverse Mortgage Transactions K Appendix K to Part 1026 Banks and Banking BUREAU OF CONSUMER FINANCIAL... transactions, as well as instructions, explanations, and examples for various transactions. This appendix...

  9. Towards constraints on fossil fuel emissions from total column carbon dioxide

    NASA Astrophysics Data System (ADS)

    Keppel-Aleks, G.; Wennberg, P. O.; O'Dell, C. W.; Wunch, D.

    2013-04-01

    We assess the large-scale, top-down constraints on regional fossil fuel emissions provided by observations of atmospheric total column CO2, XCO2. Using an atmospheric general circulation model (GCM) with underlying fossil emissions, we determine the influence of regional fossil fuel emissions on global XCO2 fields. We quantify the regional contrasts between source and upwind regions and probe the sensitivity of atmospheric XCO2 to changes in fossil fuel emissions. Regional fossil fuel XCO2 contrasts can exceed 0.7 ppm based on 2007 emission estimates, but have large seasonal variations due to biospheric fluxes. Contamination by clouds reduces the discernible fossil signatures. Nevertheless, our simulations show that atmospheric fossil XCO2 can be tied to its source region and that changes in the regional XCO2 contrasts scale linearly with emissions. We test the GCM results against XCO2 data from the GOSAT satellite. Regional XCO2 contrasts in GOSAT data generally scale with the predictions from the GCM, but the comparison is limited by the moderate precision of and relatively few observations from the satellite. We discuss how this approach may be useful as a policy tool to verify national fossil emissions, as it provides an independent, observational constraint.

  10. Effects of water regime during rice-growing season on annual direct N(2)O emission in a paddy rice-winter wheat rotation system in southeast China.

    PubMed

    Liu, Shuwei; Qin, Yanmei; Zou, Jianwen; Liu, Qiaohui

    2010-01-15

    Annual paddy rice-winter wheat rotation constitutes one of the typical cropping systems in southeast China, in which various water regimes are currently practiced during the rice-growing season, including continuous flooding (F), flooding-midseason drainage-reflooding (F-D-F), and flooding-midseason drainage-reflooding and moisture but without waterlogging (F-D-F-M). We conducted a field experiment in a rice-winter wheat rotation system to gain an insight into the water regime-specific emission factors and background emissions of nitrous oxide (N(2)O) over the whole annual cycle. While flooding led to an unpronounced N(2)O emission during the rice-growing season, it incurred substantial N(2)O emission during the following non-rice season. During the non-rice season, N(2)O fluxes were, on average, 2.61 and 2.48 mg N(2)O-Nm(-)(2) day(-1) for the 250 kg N ha(-1) applied plots preceded by the F and F-D-F water regimes, which are 56% and 49% higher than those by the F-D-F-M water regime, respectively. For the annual rotation system experienced by continuous flooding during the rice-growing season, the relationship between N(2)O emission and nitrogen input predicted the emission factor and background emission of N(2)O to be 0.87% and 1.77 kg N(2)O-Nha(-1), respectively. For the plots experienced by the water regimes of F-D-F and F-D-F-M, the emission factors of N(2)O averaged 0.97% and 0.85%, with background N(2)O emissions of 2.00 kg N(2)O-Nha(-1) and 1.61 kg N(2)O-Nha(-1) for the annual rotation system, respectively. Annual direct N(2)O-N emission was estimated to be 98.1 Gg yr(-1) in Chinese rice-based cropping systems in the 1990s, consisting of 32.3 Gg during the rice-growing season and 65.8 Gg during the non-rice season, which accounts for 25-35% of the annual total emission from croplands in China. PMID:19926115

  11. Evaluation of total volatile organic compound emissions from adhesives based on chamber tests.

    PubMed

    Guo, H; Murray, F; Wilkinson, S

    2000-02-01

    In 1997, Homeswest in western Australia and Murdoch University developed a project to construct low-allergen houses (LAHs) in a newly developed suburb. Before the construction of LAHs, all potential volatile organic compound (VOC) emission materials used in LAHs are required to be measured to ensure that they are low total VOC (TVOC) emission materials. This program was developed based on this purpose. In recent times, the number of complaints about indoor air pollution caused by VOCs has increased. A number of surveys of indoor VOCs have indicated that many indoor materials contribute to indoor air pollution. Although some studies have been conducted on the characteristics of VOC emissions from adhesives, most of them were focused on VOC emissions from floor adhesives. Few measurements of VOC emissions from adhesives used for wood, fabrics, and leather are available. Furthermore, most research on VOC emissions from adhesives has been done in countries with cool climates, where ventilation rates in the indoor environment are lower than those in Mediterranean climates, due to energy conservation. VOCs emitted from adhesives have not been sufficiently researched to prepare an emission inventory to predict indoor air quality and to determine both exposure levels for the Australian population and the most appropriate strategies to reduce exposure. An environmental test chamber with controlled temperature, relative humidity, and airflow rate was used to evaluate emissions of TVOCs from three adhesives used frequently in Australia. The quantity of TVOC emissions was measured by a gas chromatography/flame ionization detector. The primary VOCs emitted from each adhesive were detected by gas chromatography/mass spectrometry. The temporal change of TVOC concentrations emitted from each adhesive was tested. A double-exponential equation was then developed to evaluate the characteristics of TVOC emissions from these three adhesives. With this double-exponential model, the physical processes of TVOC emissions can be explained, and a variety of emission parameters can be calculated. These emission parameters could be used to estimate real indoor TVOC concentrations in Mediterranean climates. PMID:10680349

  12. [Study on estimation of deserts soil total phosphorus content from thermal-infrared emissivity].

    PubMed

    Hou, Yan-jun; Tiyip, Tashpolat; Zhang, Fei; Sawut, Mamat; Nurmemet, Ilyas

    2015-02-01

    Soil phosphorus provides nutrient elements for plants, is one of important parameters for evaluating soil quality. The traditional method for soil total phosphorus content (STPC) measurement is not effective and time-consuming. However, remote sensing (RS) enables us to determine STPC in a fast and efficient way. Studies on the estimation of STPC in near-infrared spectroscopy have been developed by scholars, but model accuracy is still poor due to the low absorption coefficient and unclear absorption peak of soil phosphorus in near-infrared. In order to solve the deficiency which thermal-infrared emissivity estimate desert soil total phosphorus content, and could improve precision of estimation deserts soil total phosphorus. In this paper, characteristics of soil thermal-infrared emissivity are analyzed on the basis of laboratory processing and spectral measurement of deserts soil samples from the eastern Junggar Basin. Furthermore, thermal-infrared emissivity based RS models for STPC estimation are established and accuracy assessed. Results show that: when STPC is higher than 0.200 g x kg(-1), the thermal-infrared emissivity increases with the increase of STPC on the wavelength between 8.00 microm and 13 microm, and the emissivity is more sensitive to STPC on the wavelength between 9.00 and 9.6 microm; the estimate mode based on multiple stepwise regression was could not to estimate deserts soil total phosphorus content from thermal-infrared emissivity because the estimation effects of them were poor. The estimation accuracy of model based on partial least squares regression is higher than the model based on multiple stepwise regression. However, the accuracy of second-order differential estimation model based on partial least square regression is higher than based on multiple stepwise regression; The first differential of continuous remove estimation model based on partial least squares regression is the best model with R2 of correction and verification are up to 0.97 and 0.82 respectively, and RMSE of correction and verification are only 0.0106 and 0.015 7 respectively, RPD is 2.62. Research results provide optimized models for remotely sensed analysis on deserts soil total phosphorus content and could realize timeliness and effective monitoring on the space-time dynamic of deserts soil total phosphorus content for future regional ecological restoration. PMID:25970891

  13. Reduction potentials of total energy consumption and GHG emissions in Xiamen

    NASA Astrophysics Data System (ADS)

    Bin, C.; Cui, S.

    2009-12-01

    Urban areas contain 40% of the population and contribute 75% of the Chinese national economy. The 35 largest cities in China, which contain 18% of the population, contribute 40% of China’s energy uses and CO2 emissions. Therefore, an insight into energy consumption and quantification of emissions from urban areas are extremely important for identifying effects of energy-saving policies and finding solution to GHG emissions in urban centers. This paper applies the Long-range Energy Alternatives Planning (LEAP) system for modeling the total energy consumption and associated emissions from Xiamen city. Energy consumption under different sets of policy and technology options are analyzed for a time span of 2007-2020 and GHG emissions are estimated. Two scenarios have been designed to describe the future strategies relating to the development of Xiamen city. The ‘Business as Usual’ scenario is used as a baseline reference scenario, in which the government is assumed to do nothing to influence the long-term trends of urban energy demand. The ‘Integrated’ scenario is considered to be the most optimized case where a series of available reduction measures such as clean energy substitution, industrial energy conservation, combined heat and power generation, energy conservation in building, motor vehicle control and new and renewable energy development and utilization are assumed to be implemented. Energy demand and GHG emissions in Xiamen up to 2020 are estimated in these two scenarios. The total reduction potentials in the ‘Integrated’ scenario and the relative contribution rate of reduction potentials of each measure have been estimated.

  14. Aircraft-Based Estimate of Total Methane Emissions from the Barnett Shale Region.

    PubMed

    Karion, Anna; Sweeney, Colm; Kort, Eric A; Shepson, Paul B; Brewer, Alan; Cambaliza, Maria; Conley, Stephen A; Davis, Ken; Deng, Aijun; Hardesty, Mike; Herndon, Scott C; Lauvaux, Thomas; Lavoie, Tegan; Lyon, David; Newberger, Tim; Pétron, Gabrielle; Rella, Chris; Smith, Mackenzie; Wolter, Sonja; Yacovitch, Tara I; Tans, Pieter

    2015-07-01

    We present estimates of regional methane (CH4) emissions from oil and natural gas operations in the Barnett Shale, Texas, using airborne atmospheric measurements. Using a mass balance approach on eight different flight days in March and October 2013, the total CH4 emissions for the region are estimated to be 76 ± 13 × 10(3) kg hr(-1) (equivalent to 0.66 ± 0.11 Tg CH4 yr(-1); 95% confidence interval (CI)). We estimate that 60 ± 11 × 10(3) kg CH4 hr(-1) (95% CI) are emitted by natural gas and oil operations, including production, processing, and distribution in the urban areas of Dallas and Fort Worth. This estimate agrees with the U.S. Environmental Protection Agency (EPA) estimate for nationwide CH4 emissions from the natural gas sector when scaled by natural gas production, but it is higher than emissions reported by the EDGAR inventory or by industry to EPA's Greenhouse Gas Reporting Program. This study is the first to show consistency between mass balance results on so many different days and in two different seasons, enabling better quantification of the related uncertainty. The Barnett is one of the largest production basins in the United States, with 8% of total U.S. natural gas production, and thus, our results represent a crucial step toward determining the greenhouse gas footprint of U.S. onshore natural gas production. PMID:26148550

  15. Daily, monthly, seasonal, and annual ammonia emissions from Southern High Plains cattle feedyards.

    PubMed

    Todd, Richard W; Cole, N Andy; Rhoades, Marty B; Parker, David B; Casey, Kenneth D

    2011-01-01

    Ammonia emitted from beef cattle feedyards adds excess reactive N to the environment, contributes to degraded air quality as a precursor to secondary particulate matter, and represents a significant loss of N from beef cattle feedyards. We used open path laser spectroscopy and an inverse dispersion model to quantify daily, monthly, seasonal, and annual NH emissions during 2 yr from two commercial cattle feedyards in the Panhandle High Plains of Texas. Annual patterns of NH fluxes correlated with air temperature, with the greatest fluxes (>100 kg ha d) during the summer and the lowest fluxes (<15 kg ha d) during the winter. Mean monthly per capita emission rate (PCER) of NH-N at one feedyard ranged from 31 g NH-N head d (January) to 207 g NH-N head d (October), when increased dietary crude protein from wet distillers grains elevated emissions. Ammonia N emissions at the other feedyard ranged from 36 g NH-N head d (January) to 121 g NH-N head d (September). Monthly fractional NH-N loss ranged from a low of 19 to 24% to a high of 80 to 85% of fed N at the two feedyards. Seasonal PCER at the two feedyards averaged 60 to 71 g NH-N head d during winter and 103 to 158 g NH-N head d during summer. Annually, PCER was 115 and 80 g NH-N head d at the two feedyards, which represented 59 and 52% of N fed to the cattle. Detailed studies are needed to determine the effect of management and environmental variables such as diet, temperature, precipitation, and manure water content on NH emissions. PMID:21712577

  16. Annual cycle and long-term trend of the methane total column in the atmosphere over the St. Petersburg region

    NASA Astrophysics Data System (ADS)

    Makarova, M. V.; Kirner, O.; Timofeev, Yu. M.; Poberovskii, A. V.; Imkhasin, Kh. Kh.; Osipov, S. I.; Makarov, B. K.

    2015-07-01

    The annual cycle and long-term trend of the methane total column in the atmosphere over the Petergof station (St. Petersburg State University) are analyzed on the basis of data obtained from Fourier-transform infrared spectrometry and EMAC-model calculations. The amplitude of the annual cycle of the total column of CH4 amounts to 2.1 and 1.5% according to experimental and model data, respectively. For the atmospheric column-averaged mole fraction of CH4, the amplitude of its annual cycle is smaller than that for its total column and amounts to 1.1 and 0.6% according to experimental and model data, respectively. The results of local continuous measurements of surface CH4 concentrations showed that, in 2013, the atmospheric column-averaged mole fractions of CH4 and the amplitudes of diurnal variations in its local concentration were characterized by the same dynamics of seasonal variations. An analysis made on the basis of simulation results showed that atmospheric conditions (under which Fourier-transform IR measurements were performed) could increase the amplitude of the annual cycle of the total column of CH4 2.5 times when compared to the true one. The results of Fourier-transform IR measurements and EMAC-model calculations showed that, during 2009-2012, the atmospheric concentration of CH4 increased at a rate of ~0.2% per year. If measurement data obtained in 2013 are added, this rate decreases to ~0.13% per year.

  17. Total suspended particulate matter emissions at high friction velocities from desert landforms

    NASA Astrophysics Data System (ADS)

    Bacon, Steven N.; McDonald, Eric V.; Amit, Rivka; Enzel, Yehouda; Crouvi, Onn

    2011-09-01

    Most wind erosion studies that characterize dust emission potential measure particulate matter smaller than 10 μm (PM10) for air quality purposes or atmospheric modeling. Because the PM10 size fraction is only a portion of the total range of fine-grained particles potentially emitted from desert landforms, we modified the miniature Portable In Situ Wind Erosion Lab (PI-SWERL) by adding a new instrument to measure total suspended particulate matter (TSP). The modified PI-SWERL is capable of measuring TSP with diameters <500 μm emitted from highly erodible surfaces at friction velocities up to 1.28 m s-1. Undisturbed and artificially disturbed surfaces of six common landforms in the Negev Desert of Israel were studied to evaluate the utility of TSP measurements. These landforms include alluvial fans and plains armored by desert pavements, loessial soils with silt-rich surficial crusts, fluvial loess with biological crusts, and active sand dunes. The landforms differ in character and surface age, thereby exhibiting a wide range of surface covers, soil properties, and soil strengths. Our results indicate that the magnitude of TSP emission is primarily controlled by geomorphic setting and surface characteristics. TSP and PM10 concentrations measured from dust-rich loessial soils were significantly correlated, and TSP emission was best predicted at all sites using PM10 content and bearing capacity. Our results demonstrate that further research is needed to determine correction factors for friction velocities related to erodible, anisotropic surface roughness elements and that the modified PI-SWERL is a promising tool to quantify total potential emission flux from desert landforms.

  18. 24 CFR 884.104 - Maximum total annual contract commitment and project account (private-owner or PHA-owner projects).

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 24 Housing and Urban Development 4 2011-04-01 2011-04-01 false Maximum total annual contract commitment and project account (private-owner or PHA-owner projects). 884.104 Section 884.104 Housing and... commitment and project account (private-owner or PHA-owner projects). (a) Maximum total annual...

  19. 24 CFR 884.104 - Maximum total annual contract commitment and project account (private-owner or PHA-owner projects).

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 24 Housing and Urban Development 4 2010-04-01 2010-04-01 false Maximum total annual contract commitment and project account (private-owner or PHA-owner projects). 884.104 Section 884.104 Housing and... commitment and project account (private-owner or PHA-owner projects). (a) Maximum total annual...

  20. Annual land cover change mapping using MODIS time series to improve emissions inventories.

    NASA Astrophysics Data System (ADS)

    López Saldaña, G.; Quaife, T. L.; Clifford, D.

    2014-12-01

    Understanding and quantifying land surface changes is necessary for estimating greenhouse gas and ammonia emissions, and for meeting air quality limits and targets. More sophisticated inventories methodologies for at least key emission source are needed due to policy-driven air quality directives. Quantifying land cover changes on an annual basis requires greater spatial and temporal disaggregation of input data. The main aim of this study is to develop a methodology for using Earth Observations (EO) to identify annual land surface changes that will improve emissions inventories from agriculture and land use/land use change and forestry (LULUCF) in the UK. First goal is to find the best sets of input features that describe accurately the surface dynamics. In order to identify annual and inter-annual land surface changes, a times series of surface reflectance was used to capture seasonal variability. Daily surface reflectance images from the Moderate Resolution Imaging Spectroradiometer (MODIS) at 500m resolution were used to invert a Bidirectional Reflectance Distribution Function (BRDF) model to create the seamless time series. Given the limited number of cloud-free observations, a BRDF climatology was used to constrain the model inversion and where no high-scientific quality observations were available at all, as a gap filler. The Land Cover Map 2007 (LC2007) produced by the Centre for Ecology & Hydrology (CEH) was used for training and testing purposes. A prototype land cover product was created for 2006 to 2008. Several machine learning classifiers were tested as well as different sets of input features going from the BRDF parameters to spectral Albedo. We will present the results of the time series development and the first exercises when creating the prototype land cover product.

  1. 40 CFR Table W - 4 of Subpart W of Part 98-Default Total Hydrocarbon Emission Factors for Underground Natural Gas...

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... Total Hydrocarbon Emission Factors for Underground Natural Gas Storage W Table W Protection of... REPORTING Petroleum and Natural Gas Systems Definitions. Pt. 98, Subpt. W, Table W-4 Table W-4 of Subpart W of Part 98—Default Total Hydrocarbon Emission Factors for Underground Natural Gas Storage...

  2. 40 CFR Table W - 2 of Subpart W of Part 98-Default Total Hydrocarbon Emission Factors for Onshore Natural Gas...

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... Total Hydrocarbon Emission Factors for Onshore Natural Gas Processing W Table W Protection of... REPORTING Petroleum and Natural Gas Systems Definitions. Pt. 98, Subpt. W, Table W-2 Table W-2 of Subpart W of Part 98—Default Total Hydrocarbon Emission Factors for Onshore Natural Gas Processing...

  3. 40 CFR Table W - 3 of Subpart W of Part 98-Default Total Hydrocarbon Emission Factors for Onshore Natural Gas...

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... Total Hydrocarbon Emission Factors for Onshore Natural Gas Transmission Compression W Table W Protection... GREENHOUSE GAS REPORTING Petroleum and Natural Gas Systems Definitions. Pt. 98, Subpt. W, Table W--3 Table W-3 of Subpart W of Part 98—Default Total Hydrocarbon Emission Factors for Onshore Natural...

  4. Recent NASA/GSFC cryogenic measurements of the total hemispheric emissivity of black surface preparations

    NASA Astrophysics Data System (ADS)

    Tuttle, J.; Canavan, E.

    2015-12-01

    High-emissivity (black) surfaces are commonly used on deep-space radiators and thermal radiation absorbers in test chambers. Since 2011 NASA Goddard Space Flight Center has measured the total hemispheric emissivity of such surfaces from 20 to 300 K using a test apparatus inside a small laboratory cryostat. We report the latest data from these measurements, including Aeroglaze Z307 paint, Black Kapton, and a configuration of painted aluminum honeycomb that was not previously tested. We also present the results of batch-to- batch reproducibility studies in Ball Infrared BlackTM and painted aluminum honeycomb. Finally, we describe a recently-adopted temperature control method which significantly speeds the data acquisition, and we discuss efforts to reduce the noise in future data.

  5. Total emissions monitoring using a multi-beam integrated real-time remote sensing system

    SciTech Connect

    Pawloski, J.N.; Gibbons, R.E.

    1997-12-31

    A large west coast refinery as part of a good neighbor agreement, contracted with Terra Air Services to design and install a real-time emissions monitoring system utilizing open-path remote sensing technologies to include FTIR, UV, and TDL units. Meteorological data is collected concurrently with emissions data. The complete system incorporates two FTIR, two UV, two laser units and six organic gas detectors. All open-path instruments are timed to scan every five minutes or less. System data can be accessed on a daily, weekly, or monthly schedule. High alarm readings are reported immediately and appropriate action taken to notify the plant and surrounding communities. A total of thirty-four toxics are monitored with the possibility of including other species of concern when required. This paper describes system layout implementation and operational functions.

  6. Estimating Total Energy Consumption and Emissions of China's Commercial and Office Buildings

    SciTech Connect

    Fridley, David; Fridley, David G.; Zheng, Nina; Zhou, Nan

    2008-03-01

    Buildings represent an increasingly important component of China's total energy consumption mix. However, accurately assessing the total volume of energy consumed in buildings is difficult owing to deficiencies in China's statistical collection system and a lack of national surveys. Official statistics suggest that buildings account for about 19% of China's total energy consumption, while others estimate the proportion at 23%, rising to 30% over the next few years. In addition to operational energy, buildings embody the energy used in the in the mining, extraction, harvesting, processing, manufacturing and transport of building materials as well as the energy used in the construction and decommissioning of buildings. This embodied energy, along with a building's operational energy, constitutes the building's life-cycle energy and emissions footprint. This report first provides a review of international studies on commercial building life-cycle energy use from which data are derived to develop an assessment of Chinese commercial building life-cycle energy use, then examines in detail two cases for the development of office building operational energy consumption to 2020. Finally, the energy and emissions implications of the two cases are presented.

  7. Scaling non-point-source mercury emissions from two active industrial gold mines: influential variables and annual emission estimates.

    PubMed

    Eckley, C S; Gustin, M; Miller, M B; Marsik, F

    2011-01-15

    Open-pit gold mines encompass thousands of hectares of disturbed materials that are often naturally enriched in mercury (Hg). The objective of this study was to estimate annual non-point-source Hg emissions from two active gold mines in Nevada. This was achieved by measuring diel and seasonally representative Hg fluxes from mesocosms of materials collected from each mine. These measurements provided a framework for scaling emissions over space and time at each mine by identifying the important variables correlated with Hg flux. The validity of these correlations was tested by comparisons with measurements conducted in situ at the mines. Of the average diel fluxes obtained in situ (92 daily flux measurements), 81% were within the 95% prediction limits of the regressions developed from the laboratory-derived data. Some surfaces at the mines could not be simulated in the laboratory setting (e.g., material actively leached by cyanide solution and tailings saturated with cyanide solution), and as such in situ data were applied for scaling. Based on the surface areas of the materials and environmental conditions at the mines during the year of study, non-point-source Hg releases were estimated to be 19 and 109 kg·year(-1). These account for 56% and 14%, respectively, of the overall emissions from each mine (point + nonpoint sources). Material being heap-leached and active tailings impoundments were the major contributors to the releases (>60% combined) suggesting that as mining operations cease, releases will decline. PMID:21142061

  8. Indoor emission, dispersion and exposure of total particle-bound polycyclic aromatic hydrocarbons during cooking

    NASA Astrophysics Data System (ADS)

    Gao, Jun; Jian, Yating; Cao, Changsheng; Chen, Lei; Zhang, Xu

    2015-11-01

    Cooking processes highly contribute to indoor polycyclic aromatic hydrocarbon (PAH) pollution. High molecular weight and potentially carcinogenic PAHs are generally found attached to small particles, i.e., particulate phase PAHs (PPAHs). Due to the fact that indoor particle dynamics have been clear, describing the indoor dynamics of cooking-generated PPAHs within a specific time span is possible. This paper attempted to quantify the dynamic emission rate, simultaneous spatial dispersion and individual exposure of PPAHs using a cooking source. Experiments were conducted in a real-scale kitchen chamber to elucidate the time-resolved emission and effect of edible oil temperature and mass. Numerical simulations based on indoor particle dynamics were performed to obtain the spatial dispersion and individual inhalation intake of PPAHs under different emission and ventilation conditions. The present work examined the preheating cooking stage, at which edible oil is heated up to beyond its smoke point. The dynamic emission rate peak point occurred much earlier than the oil heating temperature. The total PPAH emission ranged from 2258 to 6578 ng upon heating 40-85 g of edible oil. The overall intake fraction by an individual within a period of 10 min, including 3 min for heating and 7 min for natural cooling, was generally ˜1/10,000. An important outcome of this work was that the overall intake fraction could be represented by multiplying the range hood escape efficiency by the inhalation-to-ventilation rate ratio, which would be no greater than the same ratio. The methodology and results of this work were extendible for the number-based assessment of PPAHs. This work is expected to help us understand the health risks due to inhalation exposure to cooking-generated PPAHs in the kitchen.

  9. High methane emissions dominate annual greenhouse gas balances 30 years after bog rewetting

    NASA Astrophysics Data System (ADS)

    Vanselow-Algan, M.; Schmidt, S. R.; Greven, M.; Fiencke, C.; Kutzbach, L.; Pfeiffer, E.-M.

    2015-02-01

    Natural peatlands are important carbon sinks and sources of methane (CH4). In contrast, drained peatlands turn from a carbon sink to a carbon source and potentially emit nitrous oxide (N2O). Rewetting of peatlands thus implies climate change mitigation. However, data about the time span that is needed for the re-establishment of the carbon sink function by restoration is scarce. We therefore investigated the annual greenhouse gas (GHG) balances of three differently vegetated bog sites 30 years after rewetting. All three vegetation communities turned out to be sources of carbon dioxide (CO2) ranging between 0.6 ± 1.43 t CO2 ha-2 yr-1 (Sphagnum-dominated vegetation) and 3.09 ± 3.86 t CO2 ha-2 yr-1 (vegetation dominated by heath). While accounting for the different global warming potential (GWP) of the three greenhouse gases, the annual GHG balance was calculated. Emissions ranged between 25 and 53 t CO2-eq ha-1 yr-1 and were dominated by large emissions of CH4 (22 up to 51 t CO2-eq ha-1 yr-1), while highest rates were found at purple moor grass (Molinia caerulea) stands. These are to our knowledge the highest CH4 emissions so far reported for bog ecosystems in temperate Europe. As the restored area was subject to large fluctuations in water table, we conclude that the high CH4 emission rates were caused by a combination of both the temporal inundation of the easily decomposable plant litter of this grass species and the plant-mediated transport through its tissues. In addition, as a result of the land use history, the mixed soil material can serve as an explanation. With regards to the long time span passed since rewetting, we note that the initial increase in CH4 emissions due to rewetting as described in the literature is not limited to a short-term period.

  10. 77 FR 62396 - Annual Company-Run Stress Test Requirements for Banking Organizations With Total Consolidated...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-10-12

    ... Implementation of the Basel II Advanced Capital Framework, 73 FR 44620 (July 31, 2008). \\4\\ A full assessment of... Testing for Banking Organizations With More Than $10 Billion in Total Consolidated Assets, 77 FR 29458... $10 Billion in Total Consolidated Assets, 77 FR 29458 (May 14, 2012), available at...

  11. Using Total Quality To Better Manage an Institutional Research Office. AIR 1991 Annual Forum Paper.

    ERIC Educational Resources Information Center

    Heverly, Mary Ann

    Responding to the call for higher education to adopt a new paradigm in managing its administrative processes, an Institutional Research Office at Delaware County Community College (DCCC) in Pennsylvania made a two-year effort to use a Total Quality approach in its management. Total Quality Management is a Japanese movement based on the teachings…

  12. Total Quality Management on Campus: Implementation, Experiences, and Observations. ASHE Annual Meeting Paper.

    ERIC Educational Resources Information Center

    Freed, Jann E.; And Others

    A national survey of higher education institutions that have adopted Total Quality Management sought to document their implementation, principles, and results. The study developed and pre-tested a questionnaire which was then sent to 408 institutions. With a reminder post-card and a second mailing the total response rate was 67 percent or 168…

  13. COMPACT NON-CONTACT TOTAL EMISSION DETECTION FOR IN-VIVO MULTI-PHOTON EXCITATION MICROSCOPY

    PubMed Central

    Glancy, Brian; Karamzadeh, Nader S.; Gandjbakhche, Amir H.; Redford, Glen; Kilborn, Karl; Knutson, Jay R.; Balaban, Robert S.

    2014-01-01

    Summary We describe a compact, non-contact design for a Total Emission Detection (c-TED) system for intra-vital multi-photon imaging. To conform to a standard upright two-photon microscope design, this system uses a parabolic mirror surrounding a standard microscope objective in concert with an optical path that does not interfere with normal microscope operation. The non-contact design of this device allows for maximal light collection without disrupting the physiology of the specimen being examined. Tests were conducted on exposed tissues in live animals to examine the emission collection enhancement of the c-TED device compared to heavily optimized objective-based emission collection. The best light collection enhancement was seen from murine fat (5×-2× gains as a function of depth), while murine skeletal muscle and rat kidney showed gains of over two and just under two-fold near the surface, respectively. Gains decreased with imaging depth (particularly in the kidney). Zebrafish imaging on a reflective substrate showed close to a two-fold gain throughout the entire volume of an intact embryo (approximately 150 μm deep). Direct measurement of bleaching rates confirmed that the lower laser powers (enabled by greater light collection efficiency) yielded reduced photobleaching in vivo. The potential benefits of increased light collection in terms of speed of imaging and reduced photo-damage, as well as the applicability of this device to other multi-photon imaging methods is discussed. PMID:24251437

  14. Emission of submicron aerosol particles in cement kilns: Total concentration and size distribution.

    PubMed

    Rotatori, Mauro; Mosca, Silvia; Guerriero, Ettore; Febo, Antonio; Giusto, Marco; Montagnoli, Mauro; Bianchini, Massimo; Ferrero, Renato

    2015-01-01

    Cement plants are responsible for particle and gaseous emissions into the atmosphere. With respect to particle emission, the greater part of is in the range from 0.05 to 5.0 µm in diameter. In the last years attention was paid to submicron particles, but there is a lack of available data on the emission from stationary sources. In this paper, concentration and size distribution of particles emitted from four cement kilns, in relationship to operational conditions (especially the use of alternative fuel to coal) of the clinker process are reported. Experimental campaigns were carried out by measuring particles concentration and size distribution at the stack of four cement plants through condensation particle counter (CPC) and scanning mobility particle sizer spectrometer (SMPS). Average total particle number concentrations were between 2000 and 4000 particles/cm³, about 8-10 times lower that those found in the corresponding surrounding areas. As for size distribution, for all the investigated plants it is stable with a unimodal distribution (120-150 nm), independent from the fuel used. PMID:25946956

  15. Micrometeorological measurements over 3 years reveal differences in N2 O emissions between annual and perennial crops.

    PubMed

    Abalos, Diego; Brown, Shannon E; Vanderzaag, Andrew C; Gordon, Robert J; Dunfield, Kari E; Wagner-Riddle, Claudia

    2016-03-01

    Perennial crops can deliver a wide range of ecosystem services compared to annual crops. Some of these benefits are achieved by lengthening the growing season, which increases the period of crop water and nutrient uptake, pointing to a potential role for perennial systems to mitigate soil nitrous oxide (N2 O) emissions. Employing a micrometeorological method, we tested this hypothesis in a 3-year field experiment with a perennial grass-legume mixture and an annual corn monoculture. Given that N2 O emissions are strongly dependent on the method of fertilizer application, two manure application options commonly used by farmers for each crop were studied: injection vs. broadcast application for the perennial; fall vs. spring application for the annual. Across the 3 years, lower N2 O emissions (P < 0.001) were measured for the perennial compared to the annual crop, even though annual N2 O emissions increased tenfold for the perennial after ploughing. The percentage of N2 O lost per unit of fertilizer applied was 3.7, 3.1 and 1.3 times higher for the annual for each consecutive year. Differences in soil organic matter due to the contrasting root systems of these crops are probably a major factor behind the N2 O reduction. We found that a specific manure management practice can lead to increases or reductions in annual N2 O emissions depending on environmental variables. The number of freeze-thaw cycles during winter and the amount of rainfall after fertilization in spring were key factors. Therefore, general manure management recommendations should be avoided because interannual weather variability has the potential to determine if a specific practice is beneficial or detrimental. The lower N2 O emissions of perennial crops deserve further research attention and must be considered in future land-use decisions. Increasing the proportion of perennial crops in agricultural landscapes may provide an overlooked opportunity to regulate N2 O emissions. PMID:26491961

  16. 15 CFR 303.3 - Determination of the total annual duty-exemption.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... (Continued) INTERNATIONAL TRADE ADMINISTRATION, DEPARTMENT OF COMMERCE MISCELLANEOUS REGULATIONS WATCHES, WATCH MOVEMENTS AND JEWELRY PROGRAM Watches and Watch Movements 303.3 Determination of the total... the territorial watch industry and the economic interests of the territories, the...

  17. 15 CFR 303.3 - Determination of the total annual duty-exemption.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... (Continued) INTERNATIONAL TRADE ADMINISTRATION, DEPARTMENT OF COMMERCE MISCELLANEOUS REGULATIONS WATCHES, WATCH MOVEMENTS AND JEWELRY PROGRAM Watches and Watch Movements 303.3 Determination of the total... the territorial watch industry and the economic interests of the territories, the...

  18. 15 CFR 303.3 - Determination of the total annual duty-exemption.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... (Continued) INTERNATIONAL TRADE ADMINISTRATION, DEPARTMENT OF COMMERCE MISCELLANEOUS REGULATIONS WATCHES, WATCH MOVEMENTS AND JEWELRY PROGRAM Watches and Watch Movements 303.3 Determination of the total... the territorial watch industry and the economic interests of the territories, the...

  19. 15 CFR 303.3 - Determination of the total annual duty-exemption.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... (Continued) INTERNATIONAL TRADE ADMINISTRATION, DEPARTMENT OF COMMERCE MISCELLANEOUS REGULATIONS WATCHES, WATCH MOVEMENTS AND JEWELRY PROGRAM Watches and Watch Movements § 303.3 Determination of the total... the territorial watch industry and the economic interests of the territories, the...

  20. Total Quality Management: Statistics and Graphics II-Control Charts. AIR 1992 Annual Forum Paper.

    ERIC Educational Resources Information Center

    Cherland, Ryan M.

    An examination was conducted of the control chart as a quality improvement statistical method often used by Total Quality Management (TQM) practitioners in higher education. The examination used an example based on actual requests for information gathered for the Director of Human Resources at a medical center at a midwestern university. The

  1. 16 CFR 801.11 - Annual net sales and total assets.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... factory valued at $60 million. A will exchange the factory and $80 million cash for B's assets. To... acquire assets from B and add the remainder to the value of the factory. Thus, A has total assets of $65 million. Even though A will use the factory as part of the consideration for the acquisition, the value...

  2. 16 CFR 801.11 - Annual net sales and total assets.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... factory valued at $60 million. A will exchange the factory and $80 million cash for B's assets. To... acquire assets from B and add the remainder to the value of the factory. Thus, A has total assets of $65 million. Even though A will use the factory as part of the consideration for the acquisition, the value...

  3. 16 CFR 801.11 - Annual net sales and total assets.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... factory valued at $60 million. A will exchange the factory and $80 million cash for B's assets. To... acquire assets from B and add the remainder to the value of the factory. Thus, A has total assets of $65 million. Even though A will use the factory as part of the consideration for the acquisition, the value...

  4. Total Quality Management on Campus: Pipe Dream or New Paradigm? AIR 1994 Annual Forum Paper.

    ERIC Educational Resources Information Center

    Freed, Jann E.; And Others

    This study looked at how Total Quality Management (TQM) is being adopted in institutions of higher education. A questionnaire was developed seeking information on: (1) leadership of the TQM movement and timing of events; (2) the training, educating, and informing of employees; (3) specific areas using TQM and the specific statistical tools being…

  5. The Influence of Precipitation-Driven Annual Plant Growth on Dust Emission in the Mojave Desert, USA

    NASA Astrophysics Data System (ADS)

    Urban, F. E.; Reynolds, R. L.; Fulton, R. E.

    2009-12-01

    Sparsely vegetated drylands are an important source for dust emission. However, little detail is known about dust generation in response to timing of precipitation and the consequent effects on soil and vegetation dynamics in these settings. This deficiency is especially acute at intermediate landscape scales, tens of meters to several hundred meters. It is essential to consider dust emission at this scale, because it links dust generation at scales of grains and wind tunnels with regional-scale dust examined using remotely sensed data from satellites. Three sites of slightly different geomorphic settings in the vicinity of Soda (dry) Lake were instrumented (in 1999) with meteorological and sediment transport sensors to measure wind erosion through saltating particle detection during high winds. Changes in vegetation in close proximity to the instrumented sites were bi-annually documented through measurements of plant type, cover, and repeat photographic imagery. Whereas high wind events are the dominant driver of saltation and dust emission, emissive conditions prevail only when annual plants are sparse or absent. Results show that wind erosion and dust emission at two study sites are highly variable and that such variability is dominantly related to vegetation type and cover as influenced by the amount and timing of antecedent precipitation. Secondary controls on dust emission are availability of new sediment related to flood deposits at the sites and seasonally differential wind strength. At sites where annual plants respond quickly and advantageously to precipitation, emissive conditions typically shut down because of vegetation growth within two to three months. This cover of annual plants, even when dead, persists in the desert landscape as a stabilizing agent for varying amounts of time, ten months to three years depending on the amount and vegetation type and subsequent input of precipitation and further annual plant growth. The lasting stabilization effect seems to be especially strong for grasses, although exceptionally vigorous growth of forbs can produce similar results. Periods of sparse rainfall and low soil-moisture conditions at the study sites led to strong saltation activity and vulnerability to dust emission. Wet periods (relative to our period of record) stimulated annual plant growth, including in one case, excessive localized plant growth and extraordinary bloom of an invasive mustard species at one site and mediterranean grass at another. This bloom dramatically suppressed particle saltation and associated local dust emission for several years. The decade-long record at these sites documents an inter-annual succession of wet and dry conditions, thus allowing a detailed analysis of the lags and mediating influence that precipitation driven annual plant growth and subsequent decay exerts on dust emission in sparsely vegetated drylands.

  6. 40 CFR Table W - 2 of Subpart W-Default Total Hydrocarbon Emission Factors for Onshore Natural Gas Processing

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... Hydrocarbon Emission Factors for Onshore Natural Gas Processing W Table W Protection of Environment... Petroleum and Natural Gas Systems Definitions. Pt. 98, Subpt. W, Table W-2 Table W-2 of Subpart W—Default Total Hydrocarbon Emission Factors for Onshore Natural Gas Processing Onshore natural gas...

  7. 40 CFR Table W - 4 of Subpart W-Default Total Hydrocarbon Emission Factors for Underground Natural Gas Storage

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... Hydrocarbon Emission Factors for Underground Natural Gas Storage W Table W Protection of Environment... Petroleum and Natural Gas Systems Definitions. Pt. 98, Subpt. W, Table W-4 Table W-4 of Subpart W—Default Total Hydrocarbon Emission Factors for Underground Natural Gas Storage Underground natural gas...

  8. 40 CFR Table W - 3 of Subpart W-Default Total Hydrocarbon Emission Factors for Onshore Natural Gas Transmission...

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... Hydrocarbon Emission Factors for Onshore Natural Gas Transmission Compression W Table W Protection of... REPORTING Petroleum and Natural Gas Systems Definitions. Pt. 98, Subpt. W, Table W-- Table W-3 of Subpart W—Default Total Hydrocarbon Emission Factors for Onshore Natural Gas Transmission Compression...

  9. A re-appraisal of the total biomass and annual production of Antarctic krill

    NASA Astrophysics Data System (ADS)

    Atkinson, A.; Siegel, V.; Pakhomov, E. A.; Jessopp, M. J.; Loeb, V.

    2009-05-01

    Despite much research on Euphausia superba, estimates of their total biomass and production are still very uncertain. Recently, circumpolar krill databases, combined with growth models and revisions in acoustics have made it possible to refine previous estimates. Net-based databases of density and length frequency (KRILLBASE) yield a summer distributional range of ˜19×10 6 km 2 and a mean total abundance of 8×10 14 post-larvae with biomass of 379 million tonnes (Mt). These values are based on a standardised net sampling method but they average over the period 1926-2004, during which krill abundance has fluctuated. To estimate krill biomass at the end of last century we combined the KRILLBASE map of relative krill density around Antarctica with an acoustics-derived biomass estimate of 37.3 Mt derived for the Scotia Sea area in 2000 by the Commission for the Conservation of Antarctic Marine Living Resources (CCAMLR). Thus the CCAMLR 2000 survey area contains 28% of the total stock, with total biomass of ˜133 Mt in January-February 2000. Gross postlarval production is estimated conservatively at 342-536 Mt yr -1, based on three independent methods. These are high values, within the upper range of recent estimates, but consistent with the concept of high energy throughput for a species of this size. The similarity between the three production estimates reflects a broad agreement between the three growth models used, plus the fact that, for a given population size, production is relatively insensitive to the size distribution of krill at the start of the growth season. These production values lie within the envelope of what can be supported from the Southern Ocean primary production system and what is required to support an estimated predator consumption of 128-470 Mt yr -1. Given the range of recent acoustics estimates, plus the need for precautionary management of the developing krill fishery, our net-based data provide an alternative estimate of total krill biomass.

  10. Measurement of the seasonal and annual variability of total column aerosol in a northeastern U.S. network

    SciTech Connect

    Michalsky, J.J.; Schlemmer, J.A.; Harrison, L.C.; Berkheiser, W.E. III; Larson, N.R.; Laulainen, N.S.

    1994-09-01

    A network of multi-filter rotating shadowband radiometers has operated since late 1991 in the northeastern US. The data acquired are simultaneous measurements of total and diffuse horizontal irradiances in six narrowband filtered detectors and one broadband shortwave detector. The direct normal irradiances are calculated from these measurements. These direct data are corrected for cosine response and used to calculate extraterrestrial irradiance (I{sub o}) using the Langley method of regressing the natural logarithm of direct irradiance versus air mass. With frequent determinations of I{sub o}, changes in I{sub o} caused by soiling and filter degradation, for example, can be tracked. Using these I{sub o}`s, total optical depth is calculated for every clear 30-minute period in the record. Consequently, total optical depth may be obtained on a fair number of days throughout the year. Using daily average total optical depth the authors have calculated aerosol optical depths for five wavelengths by subtracting Rayleigh scattering optical depths and Chappuis ozone absorption optical depths at each wavelength. The aerosol pattern at nearly every site is an annual cycle superimposed on a decaying stratospheric loading associated with the Mount Pinatubo volcanic eruption. An attempt is made to remove the volcanic signal using data from another site.

  11. High methane emissions dominated annual greenhouse gas balances 30 years after bog rewetting

    NASA Astrophysics Data System (ADS)

    Vanselow-Algan, M.; Schmidt, S. R.; Greven, M.; Fiencke, C.; Kutzbach, L.; Pfeiffer, E.-M.

    2015-07-01

    Natural peatlands are important carbon sinks and sources of methane (CH4). In contrast, drained peatlands turn from a carbon sink to a carbon source and potentially emit nitrous oxide (N2O). Rewetting of peatlands thus potentially implies climate change mitigation. However, data about the time span that is needed for the re-establishment of the carbon sink function by restoration are scarce. We therefore investigated the annual greenhouse gas (GHG) balances of three differently vegetated sites of a bog ecosystem 30 years after rewetting. All three vegetation communities turned out to be sources of carbon dioxide (CO2) ranging between 0.6 ± 1.43 t CO2 ha-2 yr-1 (Sphagnum-dominated vegetation) and 3.09 ± 3.86 t CO2 ha-2 yr-1 (vegetation dominated by heath). While accounting for the different global warming potential (GWP) of CO2, CH4 and N2O, the annual GHG balance was calculated. Emissions ranged between 25 and 53 t CO2-eq ha-1 yr-1 and were dominated by large emissions of CH4 (22-51 t CO2-eq ha-1 yr-1), with highest rates found at purple moor grass (Molinia caerulea) stands. These are to our knowledge the highest CH4 emissions so far reported for bog ecosystems in temperate Europe. As the restored area was subject to large fluctuations in the water table, we assume that the high CH4 emission rates were caused by a combination of both the temporal inundation of the easily decomposable plant litter of purple moor grass and the plant-mediated transport through its tissues. In addition, as a result of the land use history, mixed soil material due to peat extraction and refilling can serve as an explanation. With regards to the long time span passed since rewetting, we note that the initial increase in CH4 emissions due to rewetting as described in the literature is not inevitably limited to a short-term period.

  12. Solar Total Energy Project, Shenandoah, Georgia site. Annual report, July 1979-June 1980

    SciTech Connect

    Not Available

    1980-08-01

    Progress is reported in the development of a solar total energy system for a Georgia knitwear plant. In conjunction with Sandia and others, a pier test of the design for the parabolic dishes was carried out at the solar field site. The access road to the site and the new Construction Monitoring and Visitor's Center facility have been provided. Operation of the Meteorology Station proceeded throughout the entire reporting period without significant perturbation. The major event occurred near the end of the period when the station was moved to the southeast corner of the solar field, adjacent to and just south of the trailer facilities. Efforts are described for bringing the entire data collection and energy system in the Bleyle Plant into fine tuned order. Problems with the flow channels, humidity channels and the Bleyle economizer system were traced to basic design and installation deficiencies. All associated vendors were contacted on at least one occasion throughout the period. Reasonable confidence is reported that all systems were performing to the best of their design ability, and the data system was removed in preparation for the facility move to the southeast corner of the solar site. Nominal data collection by monthly reading of the watt-hour meters in the Bleyle boiler room is reported. The Site Team continued to interface with the design teams and updated the interface drawings.The major effort involved the finalization of the power systems interface sizing design and location. Effort was also exerted in the following: support to pier testing; interconnection piping design; new trailer design and location. A large number of requests were answered in providing presentations, design data, public information and technical magazines. It is expected that when construction commences early next period, the activity will become even more intense.

  13. The Annual Cycle of Water Vapor on Mars as Observed by the Thermal Emission Spectrometer

    NASA Technical Reports Server (NTRS)

    Smith, Michael D.; Vondrak, Richard R. (Technical Monitor)

    2001-01-01

    Spectra taken by the Mars Global Surveyor Thermal Emission Spectrometer (TES) have been used to monitor the latitude, longitude, and seasonal dependence of water vapor for over one full Martian year (March 1999-March 2001). A maximum in water vapor abundance is observed at high latitudes during mid-summer in both hemispheres, reaching a maximum value of approximately 100 pr-micrometer in the north and approximately 50 pr-micrometer in the south. Low water vapor abundance (<5 pr-micrometer) is observed at middle and high latitudes in the fall and winter of both hemispheres. There are large differences in the hemispheric (north versus south) and seasonal (perihelion versus aphelion) behavior of water vapor. The latitudinal and seasonal dependence of the decay of the northern summer water vapor maximum implies cross-equatorial transport of water to the southern hemisphere, while there is little or no corresponding transport during the decay of the southern hemisphere summer maximum. The latitude-longitude dependence of annually-averaged water vapor (corrected for topography) has a significant positive correlation with albedo and significant negative correlations with thermal inertia and surface pressure. Comparison of TES results with those retrieved from the Viking Orbiter Mars Atmospheric Water Detectors (MAWD) experiments shows some similar features, but also many significant differences. The southern hemisphere maximum observed by TES was not observed by MAWD and the large latitudinal gradient in annually-averaged water vapor observed by MAWD does not appear in the TES results.

  14. Sensitivity of simulated CO2 concentration to sub-annual variations in fossil fuel CO2 emissions

    NASA Astrophysics Data System (ADS)

    Zhang, X.; Gurney, K. R.; Rayner, P.; Baker, D.; Liu, Y.-P.

    2015-07-01

    Recent advances in fossil fuel CO2 (FFCO2) emission inventories enable sensitivity tests of simulated atmospheric CO2 concentrations to sub-annual variations in FFCO2 emissions and what this implies for the interpretation of observed CO2. Six experiments are conducted to investigate the potential impact of three cycles of FFCO2 emission variability (diurnal, weekly and monthly) using a global tracer transport model. Results show an annual FFCO2 rectification varying from -1.35 to +0.13 ppm from the combination of all three cycles. This rectification is driven by a large negative diurnal FFCO2 rectification due to the covariation of diurnal FFCO2 emissions and diurnal vertical mixing, and a smaller positive seasonal FFCO2 rectification driven by the covariation of monthly FFCO2 emissions and monthly atmospheric transport. The diurnal FFCO2 emissions are responsible for a diurnal FFCO2 concentration amplitude of up to 9.12 ppm at the grid cell scale. Similarly, the monthly FFCO2 emissions are responsible for a simulated seasonal CO2 amplitude of up to 6.11 ppm at the grid cell scale. The impact of the diurnal FFCO2 emissions, when only sampled in the local afternoon is also important, causing an increase of +1.13 ppmv at the grid cell scale. The simulated CO2 concentration impacts from the diurnally and seasonally-varying FFCO2 emissions are centered over large source regions in the Northern Hemisphere, extending to downwind regions. This study demonstrates the influence of sub-annual variations in FFCO2 emissions on simulated CO2 concentration and suggests that inversion studies must take account of these variations in the affected regions.

  15. Sensitivity of simulated CO2 concentration to sub-annual variations in fossil fuel CO2 emissions

    NASA Astrophysics Data System (ADS)

    Zhang, Xia; Gurney, Kevin R.; Rayner, Peter; Baker, David; Liu, Yu-ping

    2016-02-01

    Recent advances in fossil fuel CO2 (FFCO2) emission inventories enable sensitivity tests of simulated atmospheric CO2 concentrations to sub-annual variations in FFCO2 emissions and what this implies for the interpretation of observed CO2. Six experiments are conducted to investigate the potential impact of three cycles of FFCO2 emission variability (diurnal, weekly and monthly) using a global tracer transport model. Results show an annual FFCO2 rectification varying from -1.35 to +0.13 ppm from the combination of all three cycles. This rectification is driven by a large negative diurnal FFCO2 rectification due to the covariation of diurnal FFCO2 emissions and diurnal vertical mixing, as well as a smaller positive seasonal FFCO2 rectification driven by the covariation of monthly FFCO2 emissions and monthly atmospheric transport. The diurnal FFCO2 emissions are responsible for a diurnal FFCO2 concentration amplitude of up to 9.12 ppm at the grid cell scale. Similarly, the monthly FFCO2 emissions are responsible for a simulated seasonal CO2 amplitude of up to 6.11 ppm at the grid cell scale. The impact of the diurnal FFCO2 emissions, when only sampled in the local afternoon, is also important, causing an increase of +1.13 ppmv at the grid cell scale. The simulated CO2 concentration impacts from the diurnally and seasonally varying FFCO2 emissions are centered over large source regions in the Northern Hemisphere, extending to downwind regions. This study demonstrates the influence of sub-annual variations in FFCO2 emissions on simulated CO2 concentration and suggests that inversion studies must take account of these variations in the affected regions.

  16. The Impact of HbA1c Testing on Total Annual Healthcare Expenditures Among Newly Diagnosed Patients with Diabetes

    PubMed Central

    Bhounsule, Prajakta; Peterson, Andrew M.

    2015-01-01

    Background In 2010, diabetes was the seventh leading cause of death in the United States. Diabetes also imposes a huge financial burden on the US economy. In 2009, the American Diabetes Association International Expert Committee recommended the use of the glycated hemoglobin (HbA1c) test as a uniform diagnostic measure to identify patients with diabetes. Although HbA1c is a convenient diagnostic test, it is also more expensive than older tests and could, therefore, have an impact on patients’ healthcare expenditures. Objectives To determine if HbA1c testing has an impact on total annual healthcare expenditures among newly diagnosed patients with diabetes and to analyze the factors that are associated with the total healthcare expenditures among diabetic patients before and after HbA1c was implemented as a standard diagnostic factor. Methods This was an observational, retrospective, cross-sectional study. The Medical Expenditure Panel Survey-Household Component 2009 and 2011 databases were used to form the study cohort of patients with diabetes. The total mean healthcare expenditures among patients with diabetes formed the dependent variable. A proxy variable representing a diagnosis of diabetes with and without the use of HbA1c testing in 2009 and in 2011, respectively, formed the main independent variable along with demographic factors, comorbidities, and healthcare services utilization in both years. A generalized linear regression was conducted to determine the association of HbA1c testing with total diabetes-related healthcare expenditures. Results The mean total healthcare expenditure decreased in 2011 compared with 2009. The HbA1c test did not show an association with the total healthcare expenditures versus earlier diabetes-related diagnostic factors. The total expenditures were associated with private insurance, the incidence of a previous heart attack, prescription drug refills, inpatient hospital stays, home care, hospital discharges, and visits to outpatient providers and physicians in both years. Conclusions The HbA1c diagnostic factor did not yield any association with diabetes healthcare expenditures. Although the total healthcare expenditures were reduced in 2011 compared with 2009, it cannot be established that the reduction in costs is solely attributed to the implementation of the HbA1c diagnostic criteria. Further research on healthcare expenditures for diabetic patients diagnosed with and without the use of HbA1c testing is warranted to establish any possible association. PMID:26557226

  17. Total hemispherical emissivity of very high temperature reactor (VHTR) candidate materials: Hastelloy X, Haynes 230, and Alloy 617

    NASA Astrophysics Data System (ADS)

    Maynard, Raymond K.

    An experimental system was constructed in accordance with the standard ASTM C835-06 to measure the total hemispherical emissivity of structural materials of interest in Very High Temperature Reactor (VHTR) systems. The system was tested with304 stainless steel as well as for oxidized and un-oxidized nickel, and good reproducibility and agreement with the literature data was found. Emissivity of Hastelloy X was measured under different conditions that included: (i) "as received" (original sample) from the supplier; (ii) with increased surface roughness; (iii) oxidized, and; (iv) graphite coated. Measurements were made over a wide range of temperatures. Hastelloy X, as received from the supplier, was cleaned before additional roughening of the surface and coating with graphite. The emissivity of the original samples (cleaned after received) varied from around 0.18 to 0.28 in the temperature range of 473 K to 1498 K. The apparent emissivity increased only slightly as the roughness of the surface increased (without corrections for the increased surface area due to the increased surface roughness). When Hastelloy X was coated with graphite or oxidized however, its emissivity was observed to increase substantially. With a deposited graphite layer on the Hastelloy, emissivity increased from 0.2 to 0.53 at 473 K and from 0.25 to 0.6 at 1473 K; a finding that has strong favorable safety implications in terms of decay heat removal in post-accident VHTR environments. Although initial oxidation of Hastelloy X increased the emissivity prolonged oxidation did not significantly increase emissivity. However as there is some oxidation of Hastelloy X used in the construction of VHTRs, this represents an essentially neutral finding in terms of the safety implications in post-accident VHTR environments. The total hemispherical emissivity of Haynes 230 alloy, which is regarded as a leading candidate material for heat exchangers in VHTR systems, was measured under various surface conditions. The emissivity increased from 0.178 at 600 K to 0.235 at 1375 K for Haynes 230 as received sample. The emissivity increased significantly when its surface roughness was increased, or was oxidized in air, or coated with graphite dust, as compared to the as received material. The total hemispherical emissivity of Alloy 617 was measured as a function of temperature. The total emissivity increased from about 0.2 at 600 K to about 0.35 at 1275 K.

  18. Annual nitrous oxide emissions from intensively managed soils in Maui, Hawaii

    SciTech Connect

    Zachariassen, J.; Matson, P.A.; Vitousek, P.M. NASA-Ames Research Center, Moffett Field, CA )

    1993-06-01

    High inputs of fertilizer N and other intensive cropping practices have become widespread in many agricultural areas of the tropics. In an effort to examine the effects of these practices on trace gas-atmosphere exchange we measured N[sub 2]O, CO[sub 2], and CH[sub 4] flux in a range of heavily fertilized sugar cane systems. Annual N[sub 2]O fluxes during 1992 appeared to be highest on the leeward or dry side of the island ranging from 20-40 mgN m[sup [minus]2]y[sup [minus]1]; roughly 50% of these emissions occurred during fertilization events. On the windward wet side of the island N[sub 2]O fluxes ranged from about 11-30 mgN m[sup [minus]2]y[sup [minus]1]; from 10 to 30% of these emissions occurred during fertilization events. Methane was usually taken up by these soils and variability was slightly higher on the wet side vs. the dry side; although the CO[sub 2] data set was small, flux appeared to be higher on the wet side vs. the dry side.

  19. Toxic emissions from mobile sources: a total fuel-cycle analysis for conventional and alternative fuel vehicles.

    PubMed

    Winebrake, J J; Wang, M Q; He, D

    2001-07-01

    Mobile sources are among the largest contributors of four hazardous air pollutants--benzene, 1,3-butadiene, acetaldehyde, and formaldehyde--in urban areas. At the same time, federal and state governments are promoting the use of alternative fuel vehicles as a means to curb local air pollution. As yet, the impact of this movement toward alternative fuels with respect to toxic emissions has not been well studied. The purpose of this paper is to compare toxic emissions from vehicles operating on a variety of fuels, including reformulated gasoline (RFG), natural gas, ethanol, methanol, liquid petroleum gas (LPG), and electricity. This study uses a version of Argonne National Laboratory's Greenhouse Gas, Regulated Emissions, and Energy Use in Transportation (GREET) model, appropriately modified to estimate toxic emissions. The GREET model conducts a total fuel-cycle analysis that calculates emissions from both downstream (e.g., operation of the vehicle) and upstream (e.g., fuel production and distribution) stages of the fuel cycle. We find that almost all of the fuels studied reduce 1,3-butadiene emissions compared with conventional gasoline (CG). However, the use of ethanol in E85 (fuel made with 85% ethanol) or RFG leads to increased acetaldehyde emissions, and the use of methanol, ethanol, and compressed natural gas (CNG) may result in increased formaldehyde emissions. When the modeling results for the four air toxics are considered together with their cancer risk factors, all the fuels and vehicle technologies show air toxic emission reduction benefits. PMID:15658225

  20. 1995 Idaho National Engineering Laboratory (INEL) National Emission Standards for Hazardous Air Pollutants (NESHAPs): Radionuclides. Annual report

    SciTech Connect

    1996-06-01

    Under Section 61.94 of 40 CFR 61, Subpart H (National Emission Standards for Emissions of Radionuclides Other Than Radon From Department of Energy Facilities), each DOE facility must submit an annual report documenting compliance. This report addresses the Section 61.94 reporting requirements for operations at INEL for CY 1995. For that year, airborne radionuclide emissions from INEL operations were calculated to result in a maximum individual dose to a member of the public of 1.80E-02 mrem (1.80E-07 Sievert), well below the 40 CFR 61, Subpart H, regulatory standard of 10 mrem per year (1.0E-04 Sievert per year).

  1. Assessment of air quality improvement effect under the National Total Emission Control Program during the Twelfth National Five-Year Plan in China

    NASA Astrophysics Data System (ADS)

    Xue, Wenbo; Wang, Jinnan; Niu, Hao; Yang, Jintian; Han, Baoping; Lei, Yu; Chen, Hanli; Jiang, Chunlai

    2013-04-01

    The National Total Emission Control (NTEC) Program will continue to be implemented during the 12th Five-Year Plan period (FYP, 2011-2015) in China. Two pollutants (SO2 and NOx) are covered by NTEC, of which NOx is a newly added pollutant under control. NTEC requires that the national total SO2 and NOx emissions be reduced by 8% and 10% respectively in 2015 from the levels of 2010. Annual mean SO2, NO2, and PM2.5 (sulfates and nitrates) concentrations in 2010 and 2015 were simulated with the Community Multiscale Air Quality (CMAQ) model based on the national source census data and reduction targets in the NTEC Program. Reliability of the simulation results was verified by ground-based observation data and satellite remote sensing data in 113 national key monitoring cities. The air quality improvement from NTEC was also assessed quantitatively. The assessment results indicated that the average SO2 and NO2 concentrations in all cities in 2015 would be reduced by 9.28% and 10.61% respectively from the 2010 levels. The number of cities whose annual average SO2 and NO2 concentrations fail to comply with the national ambient air quality standard will be reduced by 9 and 27 respectively. The PM2.5 simulation results demonstrated that the average sulfate and nitrate concentrations in all cities in 2010 accounted for 20.28% and 17.45% of the PM2.5 respectively. Having considered the emissions reduction effect of SO2 and NOx only, the average sulfate, nitrate, and PM2.5 concentrations in all cities in 2015 will be reduced by 6.25%, 6.04%, and 2.23% respectively from the levels of 2010. However, the annual mean PM2.5 concentration will still exceed the national standard in 77.18% of the cities in China in 2015. These percentages would be as high as 99.70% based on U.S. national standards and 100% based on the World Health Organization's guideline value.

  2. Importance of the autumn overturn and anoxic conditions in the hypolimnion for the annual methane emissions from a temperate lake.

    PubMed

    Encinas Fernández, Jorge; Peeters, Frank; Hofmann, Hilmar

    2014-07-01

    Changes in the budget of dissolved methane measured in a small temperate lake over 1 year indicate that anoxic conditions in the hypolimnion and the autumn overturn period represent key factors for the overall annual methane emissions from lakes. During periods of stable stratification, large amounts of methane accumulate in anoxic deep waters. Approximately 46% of the stored methane was emitted during the autumn overturn, contributing ∼80% of the annual diffusive methane emissions to the atmosphere. After the overturn period, the entire water column was oxic, and only 1% of the original quantity of methane remained in the water column. Current estimates of global methane emissions assume that all of the stored methane is released, whereas several studies of individual lakes have suggested that a major fraction of the stored methane is oxidized during overturns. Our results provide evidence that not all of the stored methane is released to the atmosphere during the overturn period. However, the fraction of stored methane emitted to the atmosphere during overturn may be substantially larger and the fraction of stored methane oxidized may be smaller than in the previous studies suggesting high oxidation losses of methane. The development or change in the vertical extent and duration of the anoxic hypolimnion, which can represent the main source of annual methane emissions from small lakes, may be an important aspect to consider for impact assessments of climate warming on the methane emissions from lakes. PMID:24873684

  3. Quantifying the relative contribution of natural gas fugitive emissions to total methane emissions in Colorado, Utah, and Texas using mobile isotopic methane analysis based on Cavity Ringdown Spectroscopy

    NASA Astrophysics Data System (ADS)

    Rella, Chris; Winkler, Renato; Sweeney, Colm; Karion, Anna; Petron, Gabrielle; Crosson, Eric

    2014-05-01

    Fugitive emissions of methane into the atmosphere are a major concern facing the natural gas production industry. Because methane is more energy-rich than coal per kg of carbon dioxide emitted into the atmosphere, it represents an attractive alternative to coal for electricity generation, provided that the fugitive emissions of methane are kept under control. A key step in assessing these emissions in a given region is partitioning the observed methane emissions between natural gas fugitive emissions and other sources of methane, such as from landfills or agricultural activities. One effective method for assessing the contribution of these different sources is stable isotope analysis, using the isotopic carbon signature to distinguish between natural gas and landfills or ruminants. We present measurements of methane using a mobile spectroscopic stable isotope analyzer based on cavity ringdown spectroscopy, in three intense natural gas producing regions of the United States: the Denver-Julesburg basin in Colorado, the Uintah basin in Utah, and the Barnett Shale in Texas. Performance of the CRDS isotope analyzer is presented, including precision, calibration, stability, and the potential for measurement bias due to other atmospheric constituents. Mobile isotope measurements of individual sources and in the nocturnal boundary layer have been combined to establish the fraction of the observed methane emissions that can be attributed to natural gas activities. The fraction of total methane emissions in the Denver-Julesburg basin attributed to natural gas emissions is 78 +/- 13%. In the Uinta basin, which has no other significant sources of methane, the fraction is 96% +/- 15%. In addition, results from the Barnett shale are presented, which includes a major urban center (Dallas / Ft. Worth). Methane emissions in this region are spatially highly heterogeneous. Spatially-resolved isotope and concentration measurements are interpreted using a simple emissions model to arrive at an overall isotope ratio for the region.

  4. Master trash system total particulate emission factors and rates for cotton gins

    Technology Transfer Automated Retrieval System (TEKTRAN)

    This manuscript is part of a series of manuscripts that characterize cotton gin emissions from the standpoint of stack sampling. The impetus behind this project was the urgent need to collect additional cotton gin emissions data to address current regulatory issues. A key component of this study was...

  5. Unloading system total particulate emission factors and rates for cotton gins

    Technology Transfer Automated Retrieval System (TEKTRAN)

    This manuscript is part of a series of manuscripts that characterize cotton gin emissions from the standpoint of stack sampling. The impetus behind this project was the urgent need to collect additional cotton gin emissions data to address current regulatory issues. A key component of this study was...

  6. Master trash system total particulate emission factors and rates for cotton gins: Method 17

    Technology Transfer Automated Retrieval System (TEKTRAN)

    This manuscript is part of a series of manuscripts that characterize cotton gin emissions from the standpoint of stack sampling. The impetus behind this project was the urgent need to collect additional cotton gin emissions data to address current regulatory issues. A key component of this study was...

  7. Battery condenser system total particulate emission factors and rates for cotton gins: Method 17

    Technology Transfer Automated Retrieval System (TEKTRAN)

    This manuscript is part of a series of manuscripts that characterize cotton gin emissions from the standpoint of stack sampling. The impetus behind this project was the urgent need to collect additional cotton gin emissions data to address current regulatory issues. A key component of this study was...

  8. 1st stage lint cleaning system total particulate emission factors and rates for cotton gins

    Technology Transfer Automated Retrieval System (TEKTRAN)

    This manuscript is part of a series of manuscripts that characterize cotton gin emissions from the standpoint of stack sampling. The impetus behind this project was the urgent need to collect additional cotton gin emissions data to address current regulatory issues. A key component of this study was...

  9. 1st stage seed-cotton cleaning total particulate emission factors and rates for cotton gins

    Technology Transfer Automated Retrieval System (TEKTRAN)

    This manuscript is part of a series of manuscripts that detail a project to characterize cotton gin emissions from the standpoint of stack and ambient sampling. The impetus behind the project was the urgent need to collect additional cotton gin emissions data to address current regulatory issues. A ...

  10. Mote cyclone robber system total particulate emission factors and rates for cotton gins

    Technology Transfer Automated Retrieval System (TEKTRAN)

    This manuscript is part of a series of manuscripts that characterize cotton gin emissions from the standpoint of stack sampling. The impetus behind this project was the urgent need to collect additional cotton gin emissions data to address current regulatory issues. A key component of this study was...

  11. Overflow system total particulate emission factors and rates for cotton gins

    Technology Transfer Automated Retrieval System (TEKTRAN)

    This manuscript is part of a series of manuscripts that characterize cotton gin emissions from the standpoint of stack sampling. The impetus behind this project was the urgent need to collect additional cotton gin emissions data to address current regulatory issues. A key component of this study was...

  12. Battery condenser system total particulate emission factors and rates for cotton gins

    Technology Transfer Automated Retrieval System (TEKTRAN)

    This manuscript is part of a series of manuscripts that characterize cotton gin emissions from the standpoint of stack sampling. The impetus behind this project was the urgent need to collect additional cotton gin emissions data to address current regulatory issues. A key component of this study was...

  13. Combined mote system total particulate emission factors and rates for cotton gins

    Technology Transfer Automated Retrieval System (TEKTRAN)

    This manuscript is part of a series of manuscripts that characterize cotton gin emissions from the standpoint of stack sampling. The impetus behind this project was the urgent need to collect additional cotton gin emissions data to address current regulatory issues. A key component of this study was...

  14. 2nd stage lint cleaning system total particulate emission factors and rates for cotton gins

    Technology Transfer Automated Retrieval System (TEKTRAN)

    This manuscript is part of a series of manuscripts that characterize cotton gin emissions from the standpoint of stack sampling. The impetus behind this project was the urgent need to collect additional cotton gin emissions data to address current regulatory issues. A key component of this study was...

  15. An estimation of annual nitrous oxide emissions and soil quality following the amendment of high temperature walnut shell biochar and compost to a small scale vegetable crop rotation.

    PubMed

    Suddick, Emma C; Six, Johan

    2013-11-01

    Agricultural soils are responsible for emitting large quantities of nitrous oxide (N2O). The controlled incomplete thermal decomposition of agricultural wastes to produce biochar, once amended to soils, have been hypothesized to increase crop yield, improve soil quality and reduce N2O emissions. To estimate crop yields, soil quality parameters and N2O emissions following the incorporation of a high temperature (900 °C) walnut shell (HTWS) biochar into soil, a one year field campaign with four treatments (control (CONT), biochar (B), compost (COM), and biochar+compost (B+C)) was conducted in a small scale vegetable rotation system in Northern California. Crop yields from five crops (lettuce, winter cover crop, lettuce, bell pepper and Swiss chard) were determined; there were no significant differences in yield between treatments. Biochar amended soils had significant increases in % total carbon (C) and the retention of potassium (K) and calcium (Ca). Annual cumulative N2O fluxes were not significantly different between the four treatments with emissions ranging from 0.91 to 1.12 kg N2O-N ha(-1) yr(-1). Distinct peaks of N2O occurred upon the application of N fertilizers and the greatest mean emissions, ranging from 67.04 to 151.41 g N2O-N ha(-1) day(-1), were observed following the incorporation of the winter cover crop. In conclusion, HTWS biochar application to soils had a pronounced effect on the retention of exchangeable cations such as K and Ca compared to un-amended soils and composted soils, which in turn could reduce leaching of these plant available cations and could thus improve soils with poor nutrient retention. However, HTWS biochar additions to soil had neither a positive or negative effect on crop yield nor cumulative annual emissions of N2O. PMID:23490323

  16. Total sulfur dioxide emissions and pre-eruption vapor-saturated magma at Mount St. Helens, 1980-88

    NASA Astrophysics Data System (ADS)

    Gerlach, T. M.; McGee, K. A.

    1994-12-01

    SO2 from explosive volcanism can cause significant climatic and atmospheric impacts, but the source of the sulfur is controversial. Total ozone mapping spectrometer (TOMS), correlation spectrometer (COSPEC), and ash leachate data for Mount St. Helens from the time of the climactic eruption on 18 May 1980 to the final stages of non-explosive degassing in 1988 give a total SO2 emission of 2 Mt. COSPEC data show a sharp drop in emission rate that was apparently controlled by a decreasing rate of magma supply. A total SO2 emission of only 0.08 Mt is estimated from melt inclusion data and the conventional assumption that the main sulfur source was pre-eruption melt; commonly invoked sources of 'excess sulfur' (anhydrite decomposition, basaltic magma, and degassing of non-erupted magma) are unlikely in this case. Thus melt inclusions may significantly underestimate SO2 emissions and impacts of explosive volcanism on climate and the atmosphere. Measured CO2 emissions, together with the H2O content of melt inclusions and experimental solubility data, indicate the Mount St. Helens dacite was vapor-saturated at depth prior to ascent and suggest that a vapor phase was the main source of sulfur for the 2-Mt of SO2. A vapor source is consistent with experimental studies on the Mount St. Helens dacite and removes the need for a much debated shallow magma body.

  17. 40 CFR Table W - 4 of Subpart W of Part 98-Default Total Hydrocarbon Emission Factors for Underground Natural Gas...

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 21 2014-07-01 2014-07-01 false 4 of Subpart W of Part 98-Default Total Hydrocarbon Emission Factors for Underground Natural Gas Storage W Table W Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) MANDATORY GREENHOUSE GAS REPORTING Petroleum and Natural Gas...

  18. 40 CFR Table W - 2 of Subpart W of Part 98-Default Total Hydrocarbon Emission Factors for Onshore Natural Gas...

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 21 2014-07-01 2014-07-01 false 2 of Subpart W of Part 98-Default Total Hydrocarbon Emission Factors for Onshore Natural Gas Processing W Table W Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) MANDATORY GREENHOUSE GAS REPORTING Petroleum and Natural Gas...

  19. 40 CFR Table W - 3 of Subpart W of Part 98-Default Total Hydrocarbon Emission Factors for Onshore Natural Gas...

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 21 2014-07-01 2014-07-01 false 3 of Subpart W of Part 98-Default Total Hydrocarbon Emission Factors for Onshore Natural Gas Transmission Compression W Table W Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) MANDATORY GREENHOUSE GAS REPORTING Petroleum and Natural...

  20. Particle size distribution characteristics of cotton gin third stage seed-cotton cleaning system total particulate emissions

    Technology Transfer Automated Retrieval System (TEKTRAN)

    This report is part of a project to characterize cotton gin emissions from the standpoint of total particulate stack sampling and particle size analyses. In 2013, EPA published a more stringent standard for particulate matter with nominal diameter less than or equal to 2.5 µm (PM2.5). This created a...

  1. Point source emission rate estimates from MAMAP airborne remote sensing total column observations of atmospheric CO2 and CH4

    NASA Astrophysics Data System (ADS)

    Krings, Thomas; Gerilowski, Konstantin; Buchwitz, Michael; Hartmann, Jörg; Sachs, Torsten; Erzinger, Jörg; Burrows, John P.; Bovensmann, Heinrich

    2013-04-01

    Large parts of the anthropogenic greenhouse gas emissions of CO2 and CH4 are released from localised and point sources such as power plants or as fugitive emissions from fossil fuel mining and production sites. These emissions, however, are often not readily assessed by current measurement systems and networks. A tool developed to better understand point sources of CO2 and CH4 is the optical remote sensing instrument MAMAP (Methane Airborne MAPer), operated from aircraft. After a recent instrument modification, retrievals of the column averaged dry air mole fractions for methane XCH4 (or for carbon dioxide XCO2) derived from MAMAP observations in the short-wave infrared, have a precision of about 0.4% significantly improving data quality. MAMAP total column data also serve as a testbed for inversion concepts for greenhouse gas emissions from point sources using total column atmospheric concentration measurements. As information on wind speed is an important input parameter for the inference of emission rates using MAMAP data, recent measurement campaigns comprised an in-situ wind probe operated onboard the same aircraft. Incorporation of these wind measurements in combination with model data leads to a large reduction of uncertainties on the inversion result. Using the examples of two coal mine ventilation shafts in Western Germany as well as other anthropogenic targets, the value of high resolution total column data to obtain emission rate estimates is demonstrated. MAMAP has also been tested in sunglint geometry over the ocean and has therefore the potential for application also to offshore emission sites.

  2. Ryegrass pasture combined with partial total mixed ration reduces enteric methane emissions and maintains the performance of dairy cows during mid to late lactation.

    PubMed

    Dall-Orsoletta, Aline C; Almeida, João Gabriel R; Carvalho, Paulo C F; Savian, Jean V; Ribeiro-Filho, Henrique M N

    2016-06-01

    The inclusion of grazed pasture in dairy feeding systems based on a total mixed ration (TMR) reduces feed costs, benefits herd health, and reduces environmental impact. The present study aimed to evaluate the effect of ryegrass pasture combined with a partial TMR on enteric methane emissions, dry matter intake (DMI), and performance of dairy cows from mid to late lactation. The experimental treatments included 100% TMR (control), partial TMR + 6h of continuous grazing (0900-1500 h), and partial TMR + 6h of grazing that was divided into 2 periods of 3h each that took place after milking (0900-1200 h; 1530-1830 h). Twelve F1 cows (Holstein × Jersey; 132±44 DIM) were divided into 6 lots and distributed in a 3×3 Latin square design with 3 periods of 21 d (15 d of adaptation and 6 d of evaluation). Ryegrass (Lolium multiflorum Lam.) pasture was used, and the TMR was composed of 80% corn silage, 18% soybean meal, and 2% mineral and vitamin mixture, based on dry matter. The same mixture was used for cows with access to pasture. The total DMI, milk production, and 4% fat-corrected milk were similar for all cows; however, the pasture DMI (7.4 vs. 6.0kg/d) and grazing period (+ 40 min/d) were higher in cows that had access to pasture for 2 periods of 3h compared with those that grazed for a continuous 6-h period. Methane emission was higher (656 vs. 547g/d) in confined cows than in those that received partial TMR + pasture. The inclusion of annual ryegrass pasture in the diet of dairy cows maintained animal performance and reduced enteric methane emissions. The percentage of grazed forage in the cows' diet increased when access to pasture was provided in 2 periods after the morning and afternoon milking. PMID:27016830

  3. Total sulfur dioxide emissions and pre-eruption vapor-saturated magma at Mount St. Helens, 1980-88

    SciTech Connect

    Gerlach, T.M.; McGee, K.A.

    1994-12-15

    SO{sub 2} from explosive volcanism can cause significant climatic and atmospheric impacts, but the source of the sulfur is controversial. TOMS, COSPEC, and ash leachate data for Mount St. Helens from the time of the climactic eruption on 18 May 1980 to the final stages of non-explosive degassing in 1988 give a total SO{sub 2} emission of 2 Mt. COSPEC data show a sharp drop in emission rate that was apparently controlled by a decreasing rate of magma supply. A total SO{sub 2} emission of only 0.08 Mt is estimated from melt inclusion data and the conventional assumption that the main sulfur source was pre-eruption melt; commonly invoked sources of {open_quotes}excess sulfur{close_quotes} (anhydrite decomposition, basaltic magma, and degassing of non-erupted magma) are unlikely in this case. Thus melt inclusions may significantly underestimate SO{sub 2} emissions and impacts of explosive volcanism on climate and the atmosphere. Measured CO{sub 2} emissions, together with the H{sub 2}O content of melt inclusions and experimental solubility data, indicate the Mount St. Helens dacite was vapor-saturated at depth prior to ascent and suggest that a vapor phase was the main source of sulfur for the 2-Mt of SO{sub 2}. A vapor source is consistent with experimental studies on the Mount St. Helens dacite and removes the need for a much debated shallow magma body. 23 refs., 3 figs.

  4. Quantifying the relative contribution of natural gas fugitive emissions to total methane emissions in Colorado and Utah using mobile stable isotope (13CH4) analysis

    NASA Astrophysics Data System (ADS)

    Rella, Chris; Jacobson, Gloria; Crosson, Eric; Karion, Anna; Petron, Gabrielle; Sweeney, Colm

    2013-04-01

    Fugitive emissions of methane into the atmosphere are a major concern facing the natural gas production industry. Because methane is more energy-rich than coal per kg of CO2 emitted into the atmosphere, it represents an attractive alternative to coal for electricity generation. However, given that the global warming potential of methane is many times greater than that of carbon dioxide (Solomon et al. 2007), the importance of quantifying the fugitive emissions of methane throughout the natural gas production and distribution process becomes clear (Howarth et al. 2011). A key step in the process of assessing the emissions arising from natural gas production activities is partitioning the observed methane emissions between natural gas fugitive emissions and other sources of methane, such as from landfills or agricultural activities. One effective method for assessing the contribution of these different sources is stable isotope analysis. In particular, the 13CH4 signature of natural gas (-35 to -40 permil) is significantly different that the signature of other significant sources of methane, such as landfills or ruminants (-45 to -70 permil). In this paper we present measurements of mobile field 13CH4 using a spectroscopic stable isotope analyzer based on cavity ringdown spectroscopy, in two intense natural gas producing regions of the United States: the Denver-Julesburg basin in Colorado, and the Uintah basin in Utah. Mobile isotope measurements in the nocturnal boundary layer have been made, over a total path of 100s of km throughout the regions, allowing spatially resolved measurements of the regional isotope signature. Secondly, this analyzer was used to quantify the isotopic signature of those individual sources (natural gas fugitive emissions, concentrated animal feeding operations, and landfills) that constitute the majority of methane emissions in these regions, by making measurements of the isotope ratio directly in the downwind plume from each source. These data are combined to establish the fraction of the observed methane emissions that can be attributed to natural gas activities in the regions. The fraction of total methane emissions in the Denver-Julesburg basin that can be attributed to natural gas fugitive emissions has been determined to be 71 +/- 9%. References: 1. S. Solomon, D. Qin, M. Manning, Z. Chen, M. Marquis, K.B. Averyt, M.Tignor and H.L. Miller (eds.). IPCC, 2007: Climate Change 2007: The Physical Science Basis of the Fourth Assessment Report. Cambridge University Press, Cambridge, United Kingdom and New York, NY, USA. 2. R.W. Howarth, R. Santoro, and A. Ingraffea. "Methane and the greenhouse-gas footprint of natural gas from shale formations." Climate Change, 106, 679 (2011).

  5. Sensitivity of simulated CO2 concentration to sub-annual variations in fossil fuel CO2 emissions

    NASA Astrophysics Data System (ADS)

    Zhang, X.; Gurney, K. R.; Rayner, P. J.; Baker, D. F.; Liu, Y.; Asefi-Najafabady, S.

    2014-12-01

    This study presents a sensitivity analysis of the impact of sub-annual fossil fuel CO2 emissions on simulated CO2 concentration using a global tracer transport model. Four sensitivity experiments were conducted to investigate the impact of three cyclic components (diurnal, weekly and monthly) and a complete cyclic component (the combination of the three) by comparing with a temporally "flat" fossil fuel CO2 emissions inventory. A complete exploration of these impacts is quantified at annual, seasonal, weekly and diurnal time scales of the CO2concentration for the surface, vertical profile and column-integral structure. Result shows an annual mean surface concentration difference varying from -1.35 ppm to 0.13 ppm at grid scale for the complete cyclic fossil fuel emissions, which is mainly driven by a large negative diurnal rectification and less positive seasonal rectification. The negative diurnal rectification is up to 1.45 ppm at grid scale and primarily due to the covariation of diurnal fossil fuel CO2 emissions and diurnal variations of vertical mixing. The positive seasonal rectification is up to 0.23 ppm at grid scale which is mainly driven by the monthly fossil fuel CO2emissions coupling with atmospheric transport. Both the diurnal and seasonal rectifier effects are indicated at local-to-regional scales with center at large source regions and extend to neighboring regions in mainly Northern Hemisphere. The diurnal fossil fuel CO2 emissions is found to significantly affect the simulated diurnal CO2 amplitude (up to 9.12 ppm at grid scale), which is primarily contributed by the minima concentration differences around local sunset time. Similarly, large impact on the seasonal CO2 amplitude (up to 6.11 ppm) is found at regional scale for the monthly fossil fuel emissions. An impact of diurnal fossil fuel CO2 emissions on simulated afternoon CO2 concentration is also identified by up to 1.13 ppm at local scales. The study demonstrates a large cyclic fossil fuel CO2 emissions impact on simulated CO2 concentration, and suggests that attempts to constrain carbon fluxes using surface measurements and inversion models can be improved by avoiding the biases caused by considering the temporal variations in fossil fuel CO2 emissions.

  6. Effects of organic matter amendments on net primary productivity and greenhouse gas emissions in annual grasslands.

    PubMed

    Ryals, Rebecca; Silver, Whendee L

    2013-01-01

    Most of the world's grasslands are managed for livestock production. A critical component of the long-term sustainability and profitability of rangelands (e.g., grazed grassland ecosystems) is the maintenance of plant production. Amending grassland soils with organic waste has been proposed as a means to increase net primary productivity (NPP) and ecosystem carbon (C) storage, while mitigating greenhouse gas emissions from waste management. Few studies have evaluated the effects of amendments on the C balance and greenhouse gas dynamics of grasslands. We used field manipulations replicated within and across two rangelands (a valley grassland and a coastal grassland) to determine the effects of a single application of composted green waste amendments on NPP and greenhouse gas emissions over three years. Amendments elevated total soil respiration by 18% +/- 4% at both sites but had no effect on nitrous oxide or methane emissions. Carbon losses were significantly offset by greater and sustained plant production. Amendments stimulated both above- and belowground NPP by 2.1 +/- 0.8 Mg C/ha to 4.7 +/- 0.7 Mg C/ha (mean +/- SE) over the three-year study period. Net ecosystem C storage increased by 25-70% without including the direct addition of compost C. The estimated magnitude of net ecosystem C storage was sensitive to estimates of heterotrophic soil respiration but was greater than controls in five out of six fields that received amendments. The sixth plot was the only one that exhibited lower soil moisture than the control, suggesting an important role of water limitation in these seasonally dry ecosystems. Treatment effects persisted over the course of the study, which were likely derived from increased water-holding capacity in most plots, and slow-release fertilization from compost decomposition. We conclude that a single application of composted organic matter can significantly increase grassland C storage, and that effects of a single application are likely to carry over in time. PMID:23495635

  7. Constant-Pressure Specific Heat to Hemispherical Total Emissivity Ratio for Undercooled Liquid Nickel, Zirconium, and Silicon

    NASA Technical Reports Server (NTRS)

    Rulison, Aaron J.; Rhim, Won-Kyu

    1995-01-01

    Radiative cooling curves of nickel, zirconium, and silicon melts that were obtained using the high-temperature, high-vacuum electrostatic levitator (HTHVESL) have been analyzed to determine the ratio between the constant-pressure specific heat and the hemispherical total emissivity, c(sub p)(T)epsilon(sub T)(T). This ratio determined over a wide liquid temperature range for each material allows us to determine c(sub p)(T) if epsilon(sub T)(T) is known or vice versa. Following the recipe, the hemi-spherical total emissivities for each sample at its melting temperature, epsilon(sub T)(T(sub M)), have been determined using c(sub p)(T(sub m)) values available in the literature. They are 0.15, 0.29, and 0.17, for Ni, Zr, and Si, respectively.

  8. Emissions tradeoffs among alternative marine fuels: total fuel cycle analysis of residual oil, marine gas oil, and marine diesel oil.

    PubMed

    Corbett, James J; Winebrake, James J

    2008-04-01

    Worldwide concerns about sulfur oxide (SOx) emissions from ships are motivating the replacement of marine residual oil (RO) with cleaner, lower-sulfur fuels, such as marine gas oil (MGO) and marine diesel oil (MDO). Vessel operators can use MGO and MDO directly or blended with RO to achieve environmental and economic objectives. Although expected to be much cleaner in terms of criteria pollutants, these fuels require additional energy in the upstream stages of the fuel cycle (i.e., fuel processing and refining), and thus raise questions about the net impacts on greenhouse gas emissions (primarily carbon dioxide [CO2]) because of production and use. This paper applies the Total Energy and Environmental Analysis for Marine Systems (TEAMS) model to conduct a total fuel cycle analysis of RO, MGO, MDO, and associated blends for a typical container ship. MGO and MDO blends achieve significant (70-85%) SOx emissions reductions compared with RO across a range of fuel quality and refining efficiency assumptions. We estimate CO2 increases of less than 1% using best estimates of fuel quality and refinery efficiency parameters and demonstrate how these results vary based on parameter assumptions. Our analysis suggests that product refining efficiency influences the CO2 tradeoff more than differences in the physical and energy parameters of the alternative fuels, suggesting that modest increases in CO2 could be offset by efficiency improvements at some refineries. Our results help resolve conflicting estimates of greenhouse gas tradeoffs associated with fuel switching and other emissions control policies. PMID:18422040

  9. Quantifying the relative contribution of natural gas fugitive emissions to total methane emissions in Colorado, Utah, and Texas using mobile δ13CH4 analysis

    NASA Astrophysics Data System (ADS)

    Rella, C.; Crosson, E.; Petron, G.; Sweeney, C.; Karion, A.

    2013-12-01

    Fugitive emissions of methane into the atmosphere are a major concern facing the natural gas production industry. Because methane is more energy-rich than coal per kg of CO2 emitted into the atmosphere, it represents an attractive alternative to coal for electricity generation, provided that the fugitive emissions of methane are kept under control. A key step in assessing these emissions in a given region is partitioning the observed methane emissions between natural gas fugitive emissions and other sources of methane, such as from landfills or agricultural activities. One effective method for assessing the contribution of these different sources is stable isotope analysis, using the δ13CH4 signature to distinguish between natural gas and landfills or ruminants. We present measurements of mobile field δ13CH4 using a spectroscopic stable isotope analyzer based on cavity ringdown spectroscopy, in three intense natural gas producing regions of the United States: the Denver-Julesburg basin in Colorado, the Uintah basin in Utah, and the Barnett Shale in Texas. Mobile isotope measurements of individual sources and in the nocturnal boundary layer have been combined to establish the fraction of the observed methane emissions that can be attributed to natural gas activities. The fraction of total methane emissions in the Denver-Julesburg basin attributed to natural gas emissions is 78 +/- 13%. In the Uinta basin, which has no other significant sources of methane, the fraction is 96% +/- 15%. In addition, results from the Barnett shale are presented, which includes a major urban center (Dallas / Ft. Worth). Methane emissions in this region are spatially highly heterogeneous. Spatially-resolved isotope and concentration measurements are interpreted using a simple emissions model to arrive at an overall isotope ratio for the region. (left panel) Distribution of oil and gas well pads (yellow) and landfills (blue) in the Dallas / Ft. Worth area. Mobile nocturnal measurements of methane are shown in red, indicating a strong degree of source heterogeneity. (right panel) Histogram of individual isotopic source signatures, showing distinct signatures for landfills (red) and oil and gas sources (green).

  10. Quantifying the relative contribution of natural gas fugitive emissions to total methane emissions in Weld County Colorado using δ13CH4 analysis

    NASA Astrophysics Data System (ADS)

    Rella, C.; Jacobson, G. A.; Crosson, E.; Sweeney, C.; Karion, A.; Petron, G.

    2012-12-01

    Fugitive emissions of methane into the atmosphere are a major concern facing the natural gas production industry. Given that the global warming potential of methane is many times greater than that of carbon dioxide (Forster et al. 2007), the importance of quantifying methane emissions becomes clear. Companion presentations at this meeting describe efforts to quantify the overall methane emissions in two separate gas producing areas in Colorado and Utah during intensive field campaigns undertaken in 2012. A key step in the process of assessing the emissions arising from natural gas production activities is partitioning the observed methane emissions between natural gas fugitive emissions and other sources of methane, such as from landfills or agricultural activities. One method for assessing the contribution of these different sources is stable isotope analysis. In particular, the δ13CH4 signature of natural gas (-37 permil) is significantly different that the signature of other significant sources of methane, such as landfills or ruminants (-50 to -70 permil). In this paper we present measurements of δ13CH4 in Colorado in Weld County, a region of intense natural gas production, using a mobile δ13CH4¬ analyzer capable of high-precision measurements of the stable isotope ratio of methane at ambient levels. This analyzer was used to make stable isotope measurements at a fixed location near the center of the gas producing region, from which an overall isotope ratio for the regional emissions is determined. In addition, mobile measurements in the nocturnal boundary layer have been made, over a total distance of 150 km throughout Weld County, allowing spatially resolved measurements of this isotope signature. Finally, this analyzer was used to quantify the isotopic signature of those individual sources (natural gas fugitive emissions, concentrated animal feeding operations, and landfills) that constitute the majority of methane emissions in this region, by making measurements of the isotope ratio directly in the downwind plume from each source. These data are combined to establish the fraction of the observed methane emissions that can be attributed to natural gas activities in the region. The results are compared to inventories as well as other measurement techniques, and the uncertainty of the measurement is estimated.

  11. Total energy-cycle energy and emissions impacts of hybrid electric vehicles

    SciTech Connect

    Wang, M.Q.; Plotkin, S.; Santini, D.J.; He, J.; Gaines, L.; Patterson, P.

    1997-09-17

    Argonne National Laboratory has begun an analysis of the energy and air emission impacts of hybrid electric vehicles (HEVs) over the entire energy cycle, including manufacturing, operating, and recycling the vehicles and producing their fuel. Phase 1 evaluates series HEVs using lead acid and nickel metal hydride batteries, operating independent of the electricity grid and connected to it, and compares them to conventional ICE vehicles. With efficient electric components, both grid-dependent and grid-independent vehicles are more efficient than their conventional counterpart, though most of the efficiency advantage is gained in slow, lower power operation (e.g., on the federal urban driving schedule). The grid-independent HEV is not clearly superior if it operates part of each day with grid electricity. Finally, estimates of lead emissions for the lead acid battery-powered HEV are significantly lower than suggested elsewhere.

  12. The variability of the total flux density and polarization of Jupiter's decimetric radio emission

    NASA Technical Reports Server (NTRS)

    Klein, M. J.

    1976-01-01

    Results are presented for a continuing program to monitor the Jovian 13-cm flux at weekly intervals and for an observational program to measure the linear polarization on an annual basis. The initial results of these programs are compared with existing data. Some implications about the radiation belts are discussed. When the new data are combined with previously published 11- and 21-cm measurements, it is found that the nature of the time variations during the past 13 years is similar but not identical at these wavelengths and that there is no convincing evidence that the variations are correlated with either solar activity or Jupiter's distance from the sun. The peak degree of polarization of the synchrotron has not changed more than 1% from the mean value of 24.5% during the 12-year interval considered.

  13. 1997 Idaho National Engineering and Environmental Laboratory (INEEL) National Emission Standards for Hazardous Air Pollutants (NESHAPs) -- Radionuclides annual report

    SciTech Connect

    1998-06-01

    Under Section 61.94 of Title 40, Code of Federal Regulations (CFR), Part 61, Subpart H, National Emission Standards for Emissions of Radionuclides Other Than Radon From Department of Energy Facilities, each Department of Energy (DOE) facility must submit an annual report documenting compliance. This report addresses the Section 61.94 reporting requirements for operations at the Idaho National Engineering and Environmental Laboratory (INEEL) for calendar year (CY) 1997. Section 1 of this report provides an overview of the INEEL facilities and a brief description of the radioactive materials and processes at the facilities. Section 2 identifies radioactive air effluent release points and diffuse sources at the INEEL and actual releases during 1997. Section 2 also describes the effluent control systems for each potential release point. Section 3 provides the methodology and EDE calculations for 1997 INEEL radioactive emissions.

  14. Remote sensing-based estimates of annual and seasonal emissions from crop residue burning in the contiguous United States.

    PubMed

    McCarty, Jessica L

    2011-01-01

    Crop residue burning is an extensive agricultural practice in the contiguous United States (CONUS). This analysis presents the results of a remote sensing-based study of crop residue burning emissions in the CONUS for the time period 2003-2007 for the atmospheric species of carbon dioxide (CO2), methane (CH4), carbon monoxide (CO), nitrogen dioxide (NO2, sulfur dioxide (SO2), PM2.5 (particulate matter [PM] < or = 2.5 microm in aerodynamic diameter), and PM10 (PM < or = 10 microm in aerodynamic diameter). Cropland burned area and associated crop types were derived from Moderate Resolution Imaging Spectroradiometer (MODIS) products. Emission factors, fuel load, and combustion completeness estimates were derived from the scientific literature, governmental reports, and expert knowledge. Emissions were calculated using the bottom-up approach in which emissions are the product of burned area, fuel load, and combustion completeness for each specific crop type. On average, annual crop residue burning in the CONUS emitted 6.1 Tg of CO2, 8.9 Gg of CH4, 232.4 Gg of CO, 10.6 Gg of NO2, 4.4 Gg of SO2, 20.9 Gg of PM2.5, and 28.5 Gg of PM10. These emissions remained fairly consistent, with an average interannual variability of crop residue burning emissions of +/- 10%. The states with the highest emissions were Arkansas, California, Florida, Idaho, Texas, and Washington. Most emissions were clustered in the southeastern United States, the Great Plains, and the Pacific Northwest. Air quality and carbon emissions were concentrated in the spring, summer, and fall, with an exception because of winter harvesting of sugarcane in Florida, Louisiana, and Texas. Sugarcane, wheat, and rice residues accounted for approximately 70% of all crop residue burning and associated emissions. Estimates of CO and CH4 from agricultural waste burning by the U.S. Environmental Protection Agency were 73 and 78% higher than the CO and CH4 emission estimates from this analysis, respectively. This analysis also showed that crop residue burning emissions are a minor source of CH4 emissions (< 1%) compared with the CH4 emissions from other agricultural sources, specifically enteric fermentation, manure management, and rice cultivation. PMID:21305885

  15. Forest carbon in North America: annual storage and emissions from British Columbia’s harvest, 1965–2065

    PubMed Central

    2012-01-01

    Background The default international accounting rules estimate the carbon emissions from forest products by assuming all harvest is immediately emitted to the atmosphere. This makes it difficult to assess the greenhouse gas (GHG) consequences of different forest management or manufacturing activities that maintain the storage of carbon. The Intergovernmental Panel on Climate Change (IPCC) addresses this issue by allowing other accounting methods. The objective of this paper is to provide a new model for estimating annual stock changes of carbon in harvested wood products (HWP). Results The model, British Columbia Harvested Wood Products version 1 (BC-HWPv1), estimates carbon stocks and fluxes for wood harvested in BC from 1965 to 2065, based on new parameters on local manufacturing, updated and new information for North America on consumption and disposal of wood and paper products, and updated parameters on methane management at landfills in the USA. Based on model results, reporting on emissions as they occur would substantially lower BC’s greenhouse gas inventory in 2010 from 48 Mt CO2 to 26 Mt CO2 because of the long-term forest carbon storage in-use and in the non-degradable material in landfills. In addition, if offset projects created under BC’s protocol reported 100 year cumulative emissions using the BC-HWPv1 the emissions would be lower by about 11%. Conclusions This research showed that the IPCC default methods overestimate the emissions North America wood products. Future IPCC GHG accounting methods could include a lower emissions factor (e.g. 0.52) multiplied by the annual harvest, rather than the current multiplier of 1.0. The simulations demonstrated that the primary opportunities for climate change mitigation are in shifting from burning mill waste to using the wood for longer-lived products. PMID:22828161

  16. Structure and emission of the solar chromosphere in the helium D3 line from observations of total Solar eclipses

    NASA Astrophysics Data System (ADS)

    Akimov, L. A.; Belkina, I. L.; Beletsky, S. A.; Dyatel, N. P.

    2002-04-01

    Maps of the chromospheric emission in the helium D3 line as functions of heliographic latitude and height obtained from cinematographic observations of the total solar eclipses 1972 July 10 and 1981 July 31 are presented. The helium emission is found to be observed in separate features with a characteristic supergranule size of 20000-30000 km along the limb mainly. The features are concentrated at a height of about 1400 km but can be observed at heights up to 3000-4000 km. These are also present at the base of the chromosphere, and the height distribution of surface brightness reveals two peaks at heights of about 1400 and 250 km. The energy emitted by the chromosphere over the height range of the lower maximum is about 5% and 10% of the total energy emitted by the chromosphere in the D3 line for the eclipses of 1972 and 1981, respectively. It is found that the integral brightness of the quiet chromosphere for the eclipse of 1981 was twice that of the 1972 eclipse. This difference is connected with the fact that the eclipses occurred at different phases of sunspot cycle. It is shown that the helium emission at the height range of the temperature minimum in an the inhomogeneous chromosphere can be explained by the penetration of the coronal radiation with λ<6 nm to these heights.

  17. DEVELOPMENT OF SEASONAL AND ANNUAL BIOGENIC EMISSIONS INVENTORIES FOR THE U.S. AND CANADA

    EPA Science Inventory

    The report describes the development of a biogenic emissions inventory for the U.S. and Canada, to assess the role of biogenic emissions in ozone formation. Emission inventories were developed at hourly and grid (1/4 x 116 degree) level from input data at the same scales. Emissio...

  18. Determination of total tin in canned food using inductively coupled plasma atomic emission spectroscopy.

    PubMed

    Perring, Loïc; Basic-Dvorzak, Marija

    2002-09-01

    Tin is considered to be a priority contaminant by the Codex Alimentarius Commission. Tin can enter foods either from natural sources, environmental pollution, packaging material or pesticides. Higher concentrations are found in processed food and canned foods. Dissolution of the tinplate depends on the of food matrix, acidity, presence of oxidising reagents (anthocyanin, nitrate, iron and copper) presence of air (oxygen) in the headspace, time and storage temperature. To reduce corrosion and dissolution of tin, nowadays cans are usually lacquered, which gives a marked reduction of tin migration into the food product. Due to the lack of modern validated published methods for food products, an ICP-AES (Inductively coupled plasma-atomic emission spectroscopy) method has been developed and evaluated. This technique is available in many laboratories in the food industry and is more sensitive than atomic absorption. Conditions of sample preparation and spectroscopic parameters for tin measurement by axial ICP-AES were investigated for their ruggedness. Two methods of preparation involving high-pressure ashing or microwave digestion in volumetric flasks were evaluated. They gave complete recovery of tin with similar accuracy and precision. Recoveries of tin from spiked products with two levels of tin were in the range 99+/-5%. Robust relative repeatabilities and intermediate reproducibilities were <5% for different food matrices containing >30 mg/kg of tin. Internal standard correction (indium or strontium) did not improve the method performance. Three emission lines for tin were tested (189.927, 283.998 and 235.485 nm) but only 189.927 nm was found to be robust enough with respect to interferences, especially at low tin concentrations. The LOQ (limit of quantification) was around 0.8 mg/kg at 189.927 nm. A survey of tin content in a range of canned foods is given. PMID:12324843

  19. 40 CFR 63.5870 - How do I calculate annual uncontrolled and controlled organic HAP emissions from my wet-out area...

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... control and from wet-out areas that are captured by an enclosure but are vented to the atmosphere and not... and controlled organic HAP emissions from my wet-out area(s) and from my oven(s) for continuous... annual uncontrolled and controlled organic HAP emissions from my wet-out area(s) and from my oven(s)...

  20. 40 CFR 63.5870 - How do I calculate annual uncontrolled and controlled organic HAP emissions from my wet-out area...

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... control and from wet-out areas that are captured by an enclosure but are vented to the atmosphere and not... and controlled organic HAP emissions from my wet-out area(s) and from my oven(s) for continuous... annual uncontrolled and controlled organic HAP emissions from my wet-out area(s) and from my oven(s)...

  1. 40 CFR 63.5870 - How do I calculate annual uncontrolled and controlled organic HAP emissions from my wet-out area...

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... control and from wet-out areas that are captured by an enclosure but are vented to the atmosphere and not... and controlled organic HAP emissions from my wet-out area(s) and from my oven(s) for continuous... annual uncontrolled and controlled organic HAP emissions from my wet-out area(s) and from my oven(s)...

  2. Annual emissions and air-quality impacts of an urban area district-heating system: Boston case study

    SciTech Connect

    Bernow, S.S.; McAnulty, D.R.; Buchsbaum, S.; Levine, E.

    1980-02-01

    A district-heating system, based on thermal energy from power plants retrofitted to operate in the cogeneration mode, is expected to improve local air quality. This possibility has been examined by comparing the emissions of five major atmospheric pollutants, i.e., particulates, sulfur oxides, carbon monoxide, hydrocarbons, and nitrogen oxides, from the existing heating and electric system in the City of Boston with those from a proposed district heating system. Detailed, spatial distribution of existing heating load and fuel mix is developed to specify emissions associated with existing heating systems. Actual electric-power-plant parameters and generation for the base year are specified. Additional plant fuel consumption and emissions resulting from cogeneration operation have been estimated. Six alternative fuel-emissions-control scenarios are considered. The average annual ground-level concentrations of sulfur oxides are calculated using a modified form of the EPA's Climatological Dispersion Model. This report describes the methodology, the results and their implications, and the areas for extended investigation. The initial results confirm expectations. Average sulfur oxides concentrations at various points within and near the city drop by up to 85% in the existing fuels scenarios and by 95% in scenarios in which different fuels and more-stringent emissions controls at the plants are used. These reductions are relative to concentrations caused by fuel combustion for heating and large commercial and industrial process uses within the city and Boston Edison Co. electric generation.

  3. 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.

  4. Characterization of odor emission from alternating aerobic and anoxic activated sludge systems using real-time total reduced sulfur analyzer.

    PubMed

    Kim, Hyunook; Lee, Hyunjoo; Choi, Eunsun; Choi, Il; Shin, Taesub; Im, Hyungjoon; Ahn, Soobin

    2014-12-01

    Anaerobic biodegradation of sulfur-containing compounds always generates volatile sulfur compounds (VSCs) including H2S, methyl mercaptan, and dimethyl sulfide (DMS). VSC emissions from wastewater treatment plants (WWTPs) result in odor complaints from people living nearby. To control odor-causing compounds in WWTPs, it is important to know the odor emission quantity particularly with continuous monitoring. Since modified activated sludge processes always include anaerobic, anoxic and aerobic conditions for nutrient removal, odor emission from these different environmental settings is expected. In this study, continuous monitoring of VSCs from the headspace of an alternating aerobic and anoxic (AAA) activated sludge process via total reduced sulfur (TRS) analyzer was performed. There is clear pattern of the initial TRS peak immediately after the initiation of the aeration in the AAA system and TRS concentration begins to drop through the remaining air-on cycle. On the other hand, during the air-off period, TRS concentrations increase with time. In particular, a clear inflection point in the TRS profile could be observed after complete removal of nitrate during air-off, meaning more VSCs formation. Since the highest odor emission occurs after the initiation of aeration, the future control of exhausted air should only deal with air collected during the initial aeration period (e.g., 30min), a similar concept for the treatment of first flush in combined sewer overflow. In addition, application of a control scheme to initiate aeration immediately after denitrification is completed during air-off should be beneficial in reducing odor emission. PMID:25180483

  5. Reconstruction of the net emission distribution from the total radiance distribution on a reflecting surface.

    PubMed

    Ruyten, W

    2001-01-01

    The problem is considered of reconstructing, from a measurement of the total radiance distribution on an emitting surface, the radiance distribution that would be observed in the absence of reflected radiation. An explicit solution of the implied inverse problem is derived for the case in which the reflective properties of the surface are given in terms of a bidirectional reflection distribution function. Also considered are the limiting cases of diffuse and specular reflection. Practical considerations are discussed for application of the theory to the nonintrusive and remote measurement of temperatures and pressures on concave surfaces, either by traditional radiometry or by the use of thermographic phosphors and temperature- and pressure-sensitive paints. PMID:11152000

  6. Characterizing Methane Emissions at Local Scales with a 20 Year Total Hydrocarbon Time Series, Imaging Spectrometry, and Web Facilitated Analysis

    NASA Astrophysics Data System (ADS)

    Bradley, Eliza Swan

    Methane is an important greenhouse gas for which uncertainty in local emission strengths necessitates improved source characterizations. Although CH4 plume mapping did not motivate the NASA Airborne Visible InfraRed Imaging Spectrometer (AVIRIS) design and municipal air quality monitoring stations were not intended for studying marine geological seepage, these assets have capabilities that can make them viable for studying concentrated (high flux, highly heterogeneous) CH4 sources, such as the Coal Oil Point (COP) seep field (˜0.015 Tg CH4 yr-1) offshore Santa Barbara, California. Hourly total hydrocarbon (THC) data, spanning 1990 to 2008 from an air pollution station located near COP, were analyzed and showed geologic CH4 emissions as the dominant local source. A band ratio approach was developed and applied to high glint AVIRIS data over COP, resulting in local-scale mapping of natural atmospheric CH4 plumes. A Cluster-Tuned Matched Filter (CTMF) technique was applied to Gulf of Mexico AVIRIS data to detect CH4 venting from offshore platforms. Review of 744 platform-centered CTMF subsets was facilitated through a flexible PHP-based web portal. This dissertation demonstrates the value of investigating municipal air quality data and imaging spectrometry for gathering insight into concentrated methane source emissions and highlights how flexible web-based solutions can help facilitate remote sensing research.

  7. Nondestructive Total Excitation-Emission Fluorescence Microscopy Combined with Multi-Way Chemometric Analysis for Visually Indistinguishable Single Fiber Discrimination.

    PubMed

    Muñoz de la Peña, Arsenio; Mujumdar, Nirvani; Heider, Emily C; Goicoechea, Hector C; Muñoz de la Peña, David; Campiglia, Andres D

    2016-03-01

    The potential of total excitation-emission fluorescence microscopy combined with multiway chemometric analysis was investigated for the nondestructive forensic analysis of textile fibers. The four pairs of visually indistinguishable fibers consisted of nylon 361 dyed with acid yellow 17 and acid yellow 23, acetate satin 105B dyed with disperse blue 3 and disperse blue 14, polyester 777 dyed with disperse red 1 and disperse red 19, and acrylic 864 dyed with basic green 1 and basic green 4. Excitation emission matrices were recorded with the aid of an inverted microscope and a commercial spectrofluorimeter. The full information content of excitation-emission matrices was processed with the aid of unsupervised parallel factor analysis (PARAFAC), PARAFAC supervised by linear discriminant analysis (LDA), and discriminant unfolded partial least-squares (DU-PLS). The ability of the latter algorithm to classify the four pairs of fibers demonstrates the advantage of using the multidimensionality of fluorescence data formats for the nondestructive analysis of forensic fiber evidence. PMID:26861578

  8. Miniaturized dielectric barrier discharge carbon atomic emission spectrometry with online microwave-assisted oxidation for determination of total organic carbon.

    PubMed

    Han, Bingjun; Jiang, Xiaoming; Hou, Xiandeng; Zheng, Chengbin

    2014-07-01

    A simple, rapid, and portable system consisted of a laboratory-built miniaturized dielectric barrier discharge atomic emission spectrometer and a microwave-assisted persulfate oxidation reactor was developed for sensitive flow injection analysis or continuous monitoring of total organic carbon (TOC) in environmental water samples. The standard/sample solution together with persulfate was pumped to the reactor to convert organic compounds to CO2, which was separated from liquid phase and transported to the spectrometer for detection of the elemental specific carbon atomic emission at 193.0 nm. The experimental parameters were systematically investigated. A limit of detection of 0.01 mg L(-1) (as C) was obtained based on a 10 mL sample injection volume, and the precision was better than 6.5% (relative standard deviation, RSD) at 0.1 mg L(-1). The system was successfully applied for TOC analysis of real environmental water samples. The obtained TOC value of 30 test samples agreed well with those by the standard high-temperature combustion coupled nondispersive infrared absorption method. Most importantly, the system showed good capability of in situ continuous monitoring of total organic carbon in environmental water. PMID:24862626

  9. 77 FR 24382 - Approval and Promulgation of Air Quality Implementation Plans; North Carolina; Annual Emissions...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-04-24

    ... Curran Memo further states that if an area has a previously approved emissions statements rule for the 1... stationary sources located in these areas with actual emissions of 25 tons per year or more of volatile... when the pre-existing 1-hour ozone standard was promulgated (62 FR 38855).\\1\\ \\1\\ EPA issued a...

  10. 1996 Idaho National Engineering and Environmental Laboratory (INEEL) National Emissions Standards for Hazardous Air Pollutants (NESHAPs) -- Radionuclides. Annual report

    SciTech Connect

    1997-06-01

    Under Section 61.94 of Title 40, Code of Federal Regulations (CFR), Part 61, Subpart H, ``National Emission Standards for Emissions of Radionuclides Other Than Radon From Department of Energy Facilities,`` each Department of Energy (DOE) facility must submit an annual report documenting compliance. This report addresses the Section 61.94 reporting requirements for operations at the Idaho National Engineering and Environmental Laboratory (INEEL) for calendar year (CY) 1996. The Idaho Operations Office of the DOE is the primary contact concerning compliance with the National Emission Standards for Hazardous Air Pollutants (NESHAPs) at the INEEL. For calendar year 1996, airborne radionuclide emissions from the INEEL operations were calculated to result in a maximum individual dose to a member of the public of 3.14E-02 mrem (3.14E-07 Sievert). This effective dose equivalent (EDE) is well below the 40 CFR 61, Subpart H, regulatory standard of 10 mrem per year (1.0E-04 Sievert per year).

  11. Quasi-biennial oscillation and quasi-biennial oscillation-annual beat in the tropical total column ozone: A two-dimensional model simulation

    NASA Astrophysics Data System (ADS)

    Jiang, Xun; Camp, Charles D.; Shia, Runlie; Noone, David; Walker, Christopher; Yung, Yuk L.

    2004-08-01

    The National Centers for Environmental Prediction-Department of Energy Reanalysis 2 data are used to calculate the monthly mean meridional circulation and eddy diffusivity from 1979 to 2002 for use in the California Institute of Technology-Jet Propulsion Laboratory two-dimensional (2-D) chemistry and transport model (CTM). This allows for an investigation of the impact of dynamics on the interannual variability of the tropical total column ozone for all years for which the Total Ozone Mapping Spectrometer and the Solar Backscatter Ultraviolet merged total ozone data are available. The first two empirical orthogonal functions (EOFs) of the deseasonalized and detrended stratospheric stream function capture 88% of the total variance on interannual timescales. The first EOF, accounting for over 70% of the interannual variance, is related to the quasi-biennial oscillation (QBO) and its interaction with annual cycles, the QBO-annual beat (QBO-AB). The 2-D CTM provides realistic simulations of the seasonal and interannual variability of ozone in the tropics. The equatorial ozone anomaly from the model is close to that derived from the observations. The phase and amplitude of the QBO are well captured by the model. The magnitude of the QBO signal is somewhat larger in the model than it is in the data. The QBO-AB found in the simulated ozone agrees well with that in the observed data.

  12. Needle age and season influence photosynthetic temperature response and total annual carbon uptake in mature Picea mariana trees

    DOE PAGESBeta

    Jensen, Anna M.; Warren, Jeffrey; Hanson, Paul J.; Childs, Joanne; Wullschleger, Stan D.

    2015-01-01

    Using seasonal- and cohort-specific photosynthetic temperature response functions, we quantified the physiological significance of maintaining multiple foliar cohorts in mature (~40-45 year old) Picea mariana trees in an ombrotrophic Sphagnum-bog, northern Minnesota, USA. We measured photosynthetic capacity, foliar respiration (Rd), biochemistry and morphology to estimate annual carbon (C) uptake by cohort, season and canopy position. Temperature response of key photosynthetic parameters at 25 C (i.e., light-saturated rate of CO2 assimilation (Asat), light-saturated rate of Rubisco carboxylation (Vcmax), light-saturated electron transport rate (Jmax)) were clearly dependent on season and were generally less responsive in younger needles. Temperature optimums range between 18.7-23.7,more » 31.3-38.3 and 28.7-36.7 C for Asat, Vcmax and Jmax respectively. Current-year (Y0) foliage had lower photosynthetic capacities compared to one-year-old (Y1) and two-year-old (Y2) foliage. As Y0 needles matured, values of Asat, Vcmax, Jmax, foliar LMA and nitrogen increased. Values of Vcmax, Jmax and Rd were related to foliar nitrogen but only in the youngest (Y0) cohort. Foliar ontogeny affected photosynthetic capacity more than growth temperature. Morphological and physiological cohort differences were reflected by their annual contribution to modeled C uptake, with a ~36% lower estimated annual C uptake by Y0 needles (LAI 0.52 m2m-2) compared to Y1&2 cohorts (LAI 0.67 m2m-2). Collectively, these results illustrate the physiological and ecological significance of characterizing multiple foliar cohorts during bud break and throughout the growth season, and for cumulative C uptake model estimates.« less

  13. Needle age and season influence photosynthetic temperature response and total annual carbon uptake in mature Picea mariana trees

    SciTech Connect

    Jensen, Anna M.; Warren, Jeffrey; Hanson, Paul J.; Childs, Joanne; Wullschleger, Stan D.

    2015-01-01

    Using seasonal- and cohort-specific photosynthetic temperature response functions, we quantified the physiological significance of maintaining multiple foliar cohorts in mature (~40-45 year old) Picea mariana trees in an ombrotrophic Sphagnum-bog, northern Minnesota, USA. We measured photosynthetic capacity, foliar respiration (Rd), biochemistry and morphology to estimate annual carbon (C) uptake by cohort, season and canopy position. Temperature response of key photosynthetic parameters at 25 C (i.e., light-saturated rate of CO2 assimilation (Asat), light-saturated rate of Rubisco carboxylation (Vcmax), light-saturated electron transport rate (Jmax)) were clearly dependent on season and were generally less responsive in younger needles. Temperature optimums range between 18.7-23.7, 31.3-38.3 and 28.7-36.7 C for Asat, Vcmax and Jmax respectively. Current-year (Y0) foliage had lower photosynthetic capacities compared to one-year-old (Y1) and two-year-old (Y2) foliage. As Y0 needles matured, values of Asat, Vcmax, Jmax, foliar LMA and nitrogen increased. Values of Vcmax, Jmax and Rd were related to foliar nitrogen but only in the youngest (Y0) cohort. Foliar ontogeny affected photosynthetic capacity more than growth temperature. Morphological and physiological cohort differences were reflected by their annual contribution to modeled C uptake, with a ~36% lower estimated annual C uptake by Y0 needles (LAI 0.52 m2m-2) compared to Y1&2 cohorts (LAI 0.67 m2m-2). Collectively, these results illustrate the physiological and ecological significance of characterizing multiple foliar cohorts during bud break and throughout the growth season, and for cumulative C uptake model estimates.

  14. Needle age and season influence photosynthetic temperature response and total annual carbon uptake in mature Picea mariana trees

    SciTech Connect

    Jensen, Anna M.; Warren, Jeffrey; Hanson, Paul J.; Childs, Joanne; Wullschleger, Stan D.

    2015-07-28

    Using seasonal- and cohort-specific photosynthetic temperature response functions, we quantified the physiological significance of maintaining multiple foliar cohorts in mature (~40-45 year old) Picea mariana trees in an ombrotrophic Sphagnum-bog, northern Minnesota, USA. We measured photosynthetic capacity, foliar respiration (Rd), biochemistry and morphology to estimate annual carbon (C) uptake by cohort, season and canopy position. Temperature response of key photosynthetic parameters at 25 C (i.e., light-saturated rate of CO2 assimilation (Asat), light-saturated rate of Rubisco carboxylation (Vcmax), light-saturated electron transport rate (Jmax)) were clearly dependent on season and were generally less responsive in younger needles. Temperature optimums range between 18.7-23.7, 31.3-38.3 and 28.7-36.7 C for Asat, Vcmax and Jmax respectively. Current-year (Y0) foliage had lower photosynthetic capacities compared to one-year-old (Y1) and two-year-old (Y2) foliage. As Y0 needles matured, values of Asat, Vcmax, Jmax, foliar LMA and nitrogen increased. Values of Vcmax, Jmax and Rd were related to foliar nitrogen but only in the youngest (Y0) cohort. Foliar ontogeny affected photosynthetic capacity more than growth temperature. Morphological and physiological cohort differences were reflected by their annual contribution to modeled C uptake, with a ~36% lower estimated annual C uptake by Y0 needles (LAI 0.52 m2m-2) compared to Y1&2 cohorts (LAI 0.67 m2m-2). Collectively, these results illustrate the physiological and ecological significance of characterizing multiple foliar cohorts during bud break and throughout the growth season, and for cumulative C uptake model estimates.

  15. Denitrification and N2O emissions in annual croplands, perennial grass buffers, and restored perennial grasslands

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Inclusion of perennial vegetation filter strips (PFS) in the toeslope of annual cropland watersheds can decrease nitrate (NO3) losses to ground and surface waters. Although PFS are similar to riparian buffers, PFS are a relatively new conservation tool and the processes responsible for NO3 removal f...

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

    SciTech Connect

    Stewart, Arthur J; Mosher, Jennifer J; Mulholland, Patrick J; Fortner, Allison M; Phillips, Jana Randolph; Bevelhimer, Mark S

    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 can 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.

  17. Development of a method for estimating total CH4 emission from rice paddies in Japan using the DNDC-Rice model.

    PubMed

    Katayanagi, Nobuko; Fumoto, Tamon; Hayano, Michiko; Takata, Yusuke; Kuwagata, Tsuneo; Shirato, Yasuhito; Sawano, Shinji; Kajiura, Masako; Sudo, Shigeto; Ishigooka, Yasushi; Yagi, Kazuyuki

    2016-03-15

    Methane (CH4) is a greenhouse gas, and paddy fields are one of its main anthropogenic emission sources. To mitigate this emission based on effective management measures, CH4 emission from paddy fields must be quantified at a national scale. In Japan, country-specific emission factors have been applied since 2003 to estimate national CH4 emission from paddy fields. However, this method cannot account for the effects of weather conditions and temporal variability of nitrogen fertilizer and organic matter application rates; thus, the estimated emission is highly uncertain. To improve the accuracy of national-scale estimates, we calculated country-specific emission factors using the DeNitrification-DeComposition-Rice (DNDC-Rice) model. First, we calculated CH4 emission from 1981 to 2010 using 986 datasets that included soil properties, meteorological data, and field management data. Using the simulated site-specific emission, we calculated annual mean emission for each of Japan's seven administrative regions, two water management regimes (continuous flooding and conventional mid-season drainage), and three soil drainage rates (slow, moderate, and fast). The mean emission was positively correlated with organic carbon input to the field, and we developed linear regressions for the relationships among the regions, water management regimes, and drainage rates. The regression results were within the range of published observation values for site-specific relationships between CH4 emission and organic carbon input rates. This suggests that the regressions provide a simplified method for estimating CH4 emission from Japanese paddy fields, though some modifications can further improve the estimation accuracy. PMID:26802630

  18. Indirect Estimates of the Total Gas Content of SDSS-IV/MaNGA Galaxies from Optical Emission Lines

    NASA Astrophysics Data System (ADS)

    Tremonti, Christina A.; Pace, Zachary; Andrews, Brett; Law, David R.; Li, Cheng; Martinsson, Thomas; Masters, Karen; Stark, David; Sanchez, Sebastian; Storchi-Bergmann, Thaisa; MaNGA Team

    2016-01-01

    To understand galaxy evolution it is critical to obtain a census of both the stellar and gaseous contents of galaxies. The SDSS-IV MaNGA survey will deliver exquisite stellar mass maps of ~10,000 nearby galaxies. However, radio surveys capable of providing matched resolution gas data for a large fraction of the MaNGA sample are a decade or more away. We are therefore exploring a new technique for obtaining maps of the total gas content directly from the MaNGA data. Following the method outlined in Brinchmann et al. 2013, we use the dust optical depth and the nebular metallicity measured from optical emission lines to estimate the total gas surface density in individual spaxels. We combine this with estimates of the stellar mass in each spaxel to produce spatially resolved estimates of the gas mass fraction. We compare trends in the global gas mass fraction with stellar mass and NUV-r color to those found in the literature. We explore how the radial gas mass fraction gradients of MaNGA galaxies correlate with other properties such as total stellar mass, specific star formation rate (SFR/M*), concentration, and environment.

  19. Status report and FY95 plans -- Re-evaluation of NOAA Dobson spectrophotometer total ozone data. 1994 annual report

    SciTech Connect

    1994-12-31

    The goal of this project was to re-evaluate NOAA/CMDL Dobson spectrophotometer total ozone data during FY94 from the stations Haute Provence, France; Lauder, New Zealand; Perth, Australia; and Poker Flat, Alaska and the Umkehr data from Boulder, Colorado and Mauna Loa, Hawaii. During the second year the authors planned to re-evaluate total ozone data from Byrd, Hallett and South Pole, Antarctica; Fairbanks, Alaska; Puerto Montt, Chile; Huancayo, Peru and Umkehr data from Huancayo.

  20. Evaluation of stream water quality data generated from MODIS images in modeling total suspended solid emission to a freshwater lake.

    PubMed

    Ayana, Essayas K; Worqlul, Abeyou W; Steenhuis, Tammo S

    2015-08-01

    Modeling of suspended sediment emission into freshwater lakes is challenging due to data gaps in developing countries. Existing models simulate sediment concentration at a gauging station upstream and none of these studies had modeled total suspended solids (TSS) emissions by inflowing rivers to freshwater lakes as there are no TSS measurements at the river mouth in the upper Blue Nile basin. In this study a 10year TSS time series data generated from remotely sensed MODIS/Terra images using established empirical relationship is applied to calibrate and validate a hydrology model for Lake Tana in Upper Blue Nile Basin. The result showed that at a monthly time scale TSS at the river mouth can be replicated with Nash-Sutcliffe efficiency (NS) of 0.34 for calibration and 0.21 for validation periods. Percent bias (PBIAS) and ratio of the root-mean-square error to the standard deviation of measured data (RSR) are all within range. Given the inaccessibility and costliness to measure TSS at river mouths to a lake the results found here are considered useful for suspended sediment budget studies in water bodies of the basin. PMID:25863508

  1. Solar Total-Energy Project, Shenandoah, Georgia site. Annual technical progress report, July 1, 1980-June 30, 1982

    SciTech Connect

    Not Available

    1982-01-01

    A solar total energy system is used at a knitwear manufacturing facility to supply electric power to a utility grid and process steam and air conditioning to the facility. The system is a fully cascaded total energy system with parabolic dish solar collectors and steam Rankine cycle power conversion system capable of supplying 100 to 400 kW output with process steam extraction. A detailed chronological record of activities at the facility is presented. Progress is reported in the areas of site preparation and construction support, meteorology, and information dissemination/technology transfer. Cost summaries and future plans are also given. (LEW)

  2. Total Quality Management: Statistics and Graphics III - Experimental Design and Taguchi Methods. AIR 1993 Annual Forum Paper.

    ERIC Educational Resources Information Center

    Schwabe, Robert A.

    Interest in Total Quality Management (TQM) at institutions of higher education has been stressed in recent years as an important area of activity for institutional researchers. Two previous AIR Forum papers have presented some of the statistical and graphical methods used for TQM. This paper, the third in the series, first discusses some of the…

  3. 12 CFR Appendix L to Part 226 - Assumed Loan Periods for Computations of Total Annual Loan Cost Rates

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 12 Banks and Banking 3 2013-01-01 2013-01-01 false Assumed Loan Periods for Computations of Total... Period 1 is a two-year loan period. (2) Loan Period 2 is the life expectancy in years of the youngest... 1979-1981 for females, rounded to the nearest whole year. (3) Loan Period 3 is the life...

  4. 12 CFR Appendix L to Part 226 - Assumed Loan Periods for Computations of Total Annual Loan Cost Rates

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 12 Banks and Banking 3 2011-01-01 2011-01-01 false Assumed Loan Periods for Computations of Total... Period 1 is a two-year loan period. (2) Loan Period 2 is the life expectancy in years of the youngest... 1979-1981 for females, rounded to the nearest whole year. (3) Loan Period 3 is the life...

  5. Total hydrocarbon emission testing of waste-water sludge incinerators. Volume 1. Final report 1991-92

    SciTech Connect

    Chehaske, J.T.; DeWees, W.G.; Lewis, F.M.

    1992-06-01

    The U.S. EPA is considering continuous monitoring of total hydrocarbon (THC) emissions from all wastewater sludge incincerators. The study was conducted to determine the reliability of total hydrocarbon analyzers (THCAs) in the application. Continuous monitors for oxygen (O2), carbon monoxide (CO), THC, and temperature were installed at two municipal wastewater sludge incinerators. The O2 data were used to normalize the measured THC concentrations to 7% O2. CO was measured to determine if it could be used as a surrogate for THC measurements. The two THCAs performed very well, achieving 94 and 90% on-line availability at the two sampling sites, respectively. The O2 and CO analyzers also worked well. There were initial problems with the sample conditioning system that is necessary for the CO and O2 monitors, but successful operation was achieved after it was modified. The report presents graphical and tabular summaries of the results. The report covers a period from February 1991 to September 1991, and work was completed as of May 29, 1992.

  6. Solid-Sampling Electrothermal Vaporization Inductively Coupled Plasma Optical Emission Spectrometry for Direct Determination of Total Oxygen in Coal.

    PubMed

    Vogt, Thomas; Bauer, Daniela; Nennstiel, David; Otto, Matthias

    2015-10-20

    A new analytical method for direct determination of total oxygen contents in eight coal samples of the Argonne Premium Coal (APC) series and in the NIST SRM 1632d is presented. The development of a suitable calibration procedure, optimization of measurement conditions, and the application of a tailored data processing for handling of plasma effects and high blanks enable the quantification of oxygen simultaneously with other trace, minor, or major elements in whole coal samples by means of electrothermal vaporization inductively coupled plasma optical emission spectrometry (ETV-ICP OES). For comparison, the oxygen contents were determined by a direct oxygen analyzer. The obtained oxygen values of the APC and the reference material NIST SRM 1632d were compared to data in the literature. The precision of the ETV-ICP OES was within ±3.5%, and the recovery better than 92%. With this good accuracy, the developed direct solid sampling method ETV-ICP OES is well suited for the fast determination of oxygen in coals, varying in rank from lignite to semianthracite, in a content range of about 100 ppm up to 27% using 1.5 mg sample weight. This direct analysis method represents an accurate, advantageous alternative to currently used methods for estimation of total oxygen contents in coals. PMID:26372175

  7. Non-Native Plant Litter Enhances Soil Carbon Dioxide Emissions in an Invaded Annual Grassland

    PubMed Central

    Zhang, Ling; Wang, Hong; Zou, Jianwen; Rogers, William E.; Siemann, Evan

    2014-01-01

    Litter decomposition is a fundamental ecosystem process in which breakdown and decay of plant detritus releases carbon and nutrients. Invasive exotic plants may produce litter that differs from native plant litter in quality and quantity. Such differences may impact litter decomposition and soil respiration in ways that depend on whether exotic and native plant litters decompose in mixtures. However, few field experiments have examined how exotic plants affect soil respiration via litter decomposition. Here, we conducted an in situ study of litter decomposition of an annual native grass (Eragrostis pilosa), a perennial exotic forb (Alternanthera philoxeroides), and their mixtures in an annual grassland in China to examine potential invasion effects on soil respiration. Alternanthera litter decomposed faster than Eragrostis litter when each was incubated separately. Mass loss in litter mixes was more rapid than predicted from rates in single species bags (only 35% of predicted mass remained at 8 months) showing synergistic effects. Notably, exotic plant litter decomposition rate was unchanged but native plant litter decomposition rate was accelerated in mixtures (decay constant k?=?0.20 month?1) compared to in isolation (k?=?0.10 month?1). On average, every litter type increased soil respiration compared to bare soil from which litter was removed. However, the increases were larger for mixed litter (1.82 times) than for Alternanthera litter (1.58 times) or Eragrostis litter (1.30 times). Carbon released as CO2 relative to litter carbon input was also higher for mixed litter (3.34) than for Alternathera litter (2.29) or Eragrostis litter (1.19). Our results indicated that exotic Alternanthera produces rapidly decomposing litter which also accelerates the decomposition of native plant litter in litter mixtures and enhances soil respiration rates. Thus, this exotic invasive plant species will likely accelerate carbon cycling and increase soil respiration even at intermediate stages of invasion in these annual grasslands. PMID:24647312

  8. Development of criteria for extension of applicability of low emission, high efficiency coal burners. Annual report Sep 77-Sep 78

    SciTech Connect

    Brienza, A.; Chen, S.; Heap, M.; Lee, J.; Nurick, W.

    1984-02-01

    The report gives results of the first year's effort on this contract. Experimental studies were conducted at three scales to determine the influence of coal properties on NOx emissions. In addition, the use of sorbents to reduce SOx emissions from coal flames was investigated. Bench-scale (0.1 million Btu/hr) investigation concentrated on studies to define the effect of coal characteristics on fuel nitrogen conversion. Based on these investigations, the total coal nitrogen content does not appear to be the primary variable controlling fuel NO production in pulverized-coal flames. Experiments were conducted with research-design low-NOx burners at two scales (12.5 and 100 million Btu/hr) using three coal types. Under optimum conditions, the NOx emissions, typically below 200 ppm (dry at 0% O/sub 2/), were only slightly dependent on coal characteristics. Preliminary investigations assessed the use of the low-NOx burner design to reduce NOx and SOx emissions by adding sorbents to the coal before the pulverizer. Limestone added this way gave 50, 70, and 80% reductions in SO/sub 2/ emissions at calcium/sulfur molar ratios of 1, 2, and 3, respectively.

  9. Monthly, seasonal, and annual ammonia emissions from Southern High Plains cattle feedyards

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Ammonia emitted from beef cattle feedyards adds excess reactive nitrogen to the environment and contributes to degraded air quality as a precursor to secondary particulate matter. Accurate ammonia emissions are required because, beginning in 2009, most feedyards are required by the Emergency Plannin...

  10. Inter-annual trend of the primary contribution of ship emissions to PM2.5 concentrations in Venice (Italy): Efficiency of emissions mitigation strategies

    NASA Astrophysics Data System (ADS)

    Contini, Daniele; Gambaro, Andrea; Donateo, Antonio; Cescon, Paolo; Cesari, Daniela; Merico, Eva; Belosi, Franco; Citron, Marta

    2015-02-01

    Ships and harbour emissions are currently increasing, due to the increase of tourism and trade, with potential impact on global air pollution and climate. At local scale, in-port ship emissions influence air quality in coastal areas impacting on health of coastal communities. International legislations to reduce ship emissions, both at Worldwide and European levels, are mainly based on the use of low-sulphur content fuel. In this work an analysis of the inter-annual trends of primary contribution, ε, of tourist shipping to the atmospheric PM2.5 concentrations in the urban area of Venice has been performed. Measurements have been taken in the summer periods of 2007, 2009 and 2012. Results show a decrease of ε from 7% (±1%) in 2007 to 5% (±1%) in 2009 and to 3.5% (±1%) in 2012. The meteorological and micrometeorological conditions of the campaigns were similar. Tourist ship traffic during measurement campaigns increased, in terms of gross tonnage, of about 25.4% from 2007 to 2009 and of 17.6% from 2009 to 2012. The decrease of ε was associated to the effect of a voluntary agreement (Venice Blue Flag) for the use of low-sulphur content fuel enforced in the area between 2007 and 2009 and to the implementation of the 2005/33/CE Directive in 2010. Results show that the use of low-sulphur fuel could effectively reduce the impact of shipping to atmospheric primary particles at local scale. Further, voluntary agreement could also be effective in reducing the impact of shipping on local air quality in coastal areas.

  11. Annual emissions of mercury to the atmosphere from natural sources in Nevada and California

    USGS Publications Warehouse

    Coolbaugh, M.F.; Gustin, M.S.; Rytuba, J.J.

    2002-01-01

    The impact of natural source emissions on atmospheric mercury concentrations and the biogeochemical cycle of mercury is not known. To begin to assess this impact, mercury emissions to the atmosphere were scaled up for three areas naturally enriched in mercury: the Steamboat Springs geothermal area, Nevada, the New Idria mercury mining district, California, and the Medicine Lake volcano, California. Data used to scale up area emissions included mercury fluxes, measured in-situ using field flux chambers, from undisturbed and disturbed geologic substrates, and relationships between mercury emissions and geologic rock types, soil mercury concentrations, and surface heat flux. At select locations mercury fluxes were measured for 24 h and the data were used to adjust fluxes measured at different times of the day to give an average daily flux. This adjustment minimized daily temporal variability, which is observed for mercury flux because of light and temperature effects. Area emissions were scaled spatially and temporally with GIS software. Measured fluxes ranged from 0.3 to approximately 50 ng m-2 h-1 at undisturbed sites devoid of mercury mineralization, and to greater than 10,000 ng m-2 h-1 from substrates that were in areas of mercury mining. Area-averaged fluxes calculated for bare soil at Steamboat Springs, New Idria, and Medicine Lake of 181, 9.2, and 2 ng m-2 h-1, respectively, are greater than fluxes previously ascribed to natural non-point sources, indicating that these sources may be more significant contributors of mercury to the atmosphere than previously realized.

  12. Solar Total Energy Project, Shenandoah, Georgia site. Annual technical progress report, July 1, 1982-June 30, 1983

    SciTech Connect

    Not Available

    1983-01-01

    A part of the National Solar Thermal Energy Program, initially funded by DOE, the Shenandoah Project, is the world's largest industrial application of the solar total energy concept. The objective of the Project is to evaluate a solar total energy system that provides electrical power, process steam, and air conditioning for a knit-wear factory (operated by Bleyle of America, Inc.). During normal operation, solar energy generates a large part of the electricity and displaces part of the fossil fuels normally used to run the factory and produce the clothing. Construction of the system was completed early in 1982, when operations were initiated. Solution of unexpected electrical and mechanical problems produced significant information for subsequent system designs. An overview of the Project and a brief System Description is presented following a chronological summary of progress. A discussion of varius anomalies, together with subsequent high quality solar and thermodynamic system performance results, is then discussed.

  13. Solar Total Energy Project, Shenandoah, Georgia site. Annual technical progress report, July 1, 1983-June 30, 1984

    SciTech Connect

    Ney, E.J.

    1984-10-01

    The Solar Total Energy Project (STEP) at Shenandoah, Georgia, is a cooperative effort between the United States Department of Energy (DOE) and the Georgia Power Company to further the search for new sources of energy. A part of the National Solar Thermal Energy Program, initially funded by DOE, the Shenandoah Project, is the world's largest industrial application of the solar total energy concept. The objective of the Project is to evaluate a solar total energy system that provides electrical power, process steam, and air conditioning for a knit-wear factory (operated by Bleyle of America, Inc.). During normal operation, solar energy generates a large part of the electricity and displaces part of the fossil fuels normally used to run the factory and produce the clothing. Construction of the system was completed early in 1982, when operations were initiated. Solution of unexpected electrical and mechanical problems produced significant information for subsequent system designs. A discussion of various anomalies, together with subsequent high quality solar and thermodynamic system performance results, is included.

  14. 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.

  15. Estimates of global, regional, and national annual CO{sub 2} emissions from fossil-fuel burning, hydraulic cement production, and gas flaring: 1950--1992

    SciTech Connect

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

    1995-12-01

    This document describes the compilation, content, and format of the most comprehensive C0{sub 2}-emissions database currently available. The database includes global, regional, and national annual estimates of C0{sub 2} emissions resulting from fossil-fuel burning, cement manufacturing, and gas flaring in oil fields for 1950--92 as well as the energy production, consumption, and trade data used for these estimates. The methods of Marland and Rotty (1983) are used to calculate these emission estimates. For the first time, the methods and data used to calculate CO, emissions from gas flaring are presented. This C0{sub 2}-emissions database is useful for carbon-cycle research, provides estimates of the rate at which fossil-fuel combustion has released C0{sub 2} to the atmosphere, and offers baseline estimates for those countries compiling 1990 C0{sub 2}-emissions inventories.

  16. Significant non-linearity in nitrous oxide chamber data and its effect on calculated annual emissions

    NASA Astrophysics Data System (ADS)

    Stolk, P. C.; Jacobs, C. M. J.; Moors, E. J.; Hensen, A.; Velthof, G. L.; Kabat, P.

    2009-01-01

    Chambers are widely used to measure surface fluxes of nitrous oxide (N2O). Usually linear regression is used to calculate the fluxes from the chamber data. Non-linearity in the chamber data can result in an underestimation of the flux. Non-linear regression models are available for these data, but are not commonly used. In this study we compared the fit of linear and non-linear regression models to determine significant non-linearity in the chamber data. We assessed the influence of this significant non-linearity on the annual fluxes. For a two year dataset from an automatic chamber we calculated the fluxes with linear and non-linear regression methods. Based on the fit of the methods 32% of the data was defined significant non-linear. Significant non-linearity was not recognized by the goodness of fit of the linear regression alone. Using non-linear regression for these data and linear regression for the rest, increases the annual flux with 21% to 53% compared to the flux determined from linear regression alone. We suggest that differences this large are due to leakage through the soil. Macropores or a coarse textured soil can add to fast leakage from the chamber. Yet, also for chambers without leakage non-linearity in the chamber data is unavoidable, due to feedback from the increasing concentration in the chamber. To prevent a possibly small, but systematic underestimation of the flux, we recommend comparing the fit of a linear regression model with a non-linear regression model. The non-linear regression model should be used if the fit is significantly better. Open questions are how macropores affect chamber measurements and how optimization of chamber design can prevent this.

  17. Seasonal and inter-annual variability in wetland methane emissions simulated by CLM4Me' and CAM-chem and comparisons to observations of concentrations

    NASA Astrophysics Data System (ADS)

    Meng, L.; Paudel, R.; Hess, P. G. M.; Mahowald, N. M.

    2015-02-01

    Understanding the temporal and spatial variation of wetland methane emissions is essential to the estimation of the global methane budget. We examine the seasonal and inter-annual variability in wetland methane emissions simulated in the Community Land Model (CLM4Me'). Methane emissions from both the Carbon-Nitrogen (CN, i.e. CLM4.0) and the Biogeochemistry (BGC, i.e. CLM4.5) versions of the CLM are evaluated. We further conduct simulations of the transport and removal of methane using the Community Atmosphere Model (CAM-chem) model using CLM4Me' methane emissions from both CN and BGC along with other methane sources and compare model simulated atmospheric methane concentration with observations. In addition, we simulate the atmospheric concentrations based on the TransCom wetland and rice paddy emissions from a different terrestrial ecosystem model VISIT. Our analysis suggests CN wetland methane emissions are higher in tropics and lower in high latitudes than BGC. In CN, methane emissions decrease from 1993 to 2004 while this trend does not appear in the BGC version. In the CN versions, methane emission variations follow satellite-derived inundation wetlands closely. However, they are dissimilar in BGC due to its different carbon cycle. CAM-chem model simulations with CLM4Me' methane emissions suggest that both prescribed anthropogenic and predicted wetlands methane emissions contribute substantially to seasonal and inter-annual variability in atmospheric methane concentration. It also suggests that different spatial patterns of wetland emissions can have significant impacts on N-S atmospheric CH4 concentration gradients and growth rates. This study suggests that large uncertainties still exist in terms of spatial patterns and magnitude of global wetland methane budgets, and that substantial uncertainty comes from the carbon model underlying the methane flux modules.

  18. The Eighth Annual NASA/Contractors Conference and 1991 National Symposium on Quality and Productivity: Extending the boundaries of total quality management

    NASA Technical Reports Server (NTRS)

    Templeton, Geoffrey B. (Editor); Stewart, Lynne M. (Editor); Still, William T. (Editor)

    1992-01-01

    The Eighth Annual NASA/Contractors Conference and 1991 National Symposium on Quality and Productivity provided a forum to exchange knowledge and experiences in these areas of continuous improvement. The more than 1,100 attendees from government, industry, academia, community groups, and the international arena had a chance to learn about methods, tools, and strategies for excellence and to discuss continuous improvement strategies, successes, and failures. This event, linked via satellite to concurrent conferences hosted by the NASA Goddard Space Flight Center in Greenbelt, Maryland, and Martin Marietta Astronautics Group in Denver, Colorado, also explored extending the boundaries of Total Quality Management to include partnerships for quality within communities and encouraged examination, evaluation, and change to incorporate the principles of continuous improvement.

  19. Relative contribution of oxygenated hydrocarbons to the total biogenic VOC emissions of selected mid-European agricultural and natural plant species

    NASA Astrophysics Data System (ADS)

    König, Georg; Brunda, Monika; Puxbaum, Hans; Hewitt, C. Nicholas; Duckham, S. Craig; Rudolph, Jochen

    Emission rates of more than 50 individual VOCs were determined for eight plant species and three different types of grass land typical for natural deciduous and agricultural vegetation in Austria. In addition to the emissions of isoprene and monoterpenes, 33 biogenic oxygenated volatile organic compounds (BOVOCs) were detected. Of these, 2-methyl-l-propanol, 1-butanal, 2-butanal, 1-pentanol, 3-pentanol, 1-hexanol, 6-methyl-5-hepten-2-one, butanal and ethylhexylacetate were observed for the first time as plant emissions. In terms of prevalence of one of the groups of emitted VOCs (isoprene, terpenes, BOVOCs) the grain plants wheat and rye, grape, oilseed rape and the decidous trees hombeam and birch could be classified as "BOVOC"-emitters. For the grass plots examined, BOVOCs and terpenes appear to be of equal importance. The emission rates of the total assigned organic plant emissions ranged from 0.01 μ g -1 h -1 for wheat to 0.8 μg g -1 h -1 for oak (based on dry leaf weight). Intercomparison with available data from other studies show that our emission rates are rather at the lower end of reported ranges. The influence of the stage of growth was examined for rye, rape (comparing emissions of blossoming and nonblossoming plants) and for grape (with and without fruit). Emission rate differences for different stages of growth varied from nondetectable for blossoming and nonblossoming rye to a factor of six for the grape with fruits vs grape without fruits (emission rate based on dry leaf weight). The major decidous tree in Austria (beech) is a terpene emitter, with the contribution of BOVOCs below 5% of the total assigned emissions of 0.2 μg g -1 h -1 for the investigations of 20°C.

  20. Research of Ionospheric Total Electron Content Variations Caused by Powerful Radio Emission of `SURA' Facility on Network of Gnss - Receivers

    NASA Astrophysics Data System (ADS)

    Kogogin, Denis; Nasyrov, Igor; Grach, Savely; Shindin, Alexey; Zagretdinov, Renat; Shaimukhametov, Ramil; Kislichin, Alexander; Ryabova, Mariya

    Large-scale irregularities with scales of 5-50 km can be effectively studied using dual-frequency raying by signals of the Navstar (GPS) and GLONASS microwave satellite systems. During propagation through the heated region, such signals acquire an additional phase increment stipulated by the dispersion of radio waves in the ionospheric plasma and linearly related to the total electron content (TEC) on the propagation trajectory. In this work we present results of measurement of total electron content (TEC) variations in the F2 part of the ionosphere of the Earth caused by powerful radio emission of “Sura” facility carried out during several experimental companies from 2010 to 2013 years. Parameters of TEC-variations were obtained by dual - frequency global navigation satellite systems (GNSS) diagnostics. Registration of signal parameters from GNSS-transmitters was performed at spatially separated sites around the “Sura” facility: Vasilsursk (56(°) 08' N, 46(°) 05' E), Zelenodolsk (55(°) 52' N, 48(°) 33' E), Kazan (55(°) 48' N, 49(°) 08' E) and Yoshkar-Ola (56(°) 38'N, 47(°) 52'E). The initial data containing measurements of the phase L and pseudorange P for the operating frequencies f1 =1575.42 MHz and f2 = 1227.60 MHz are RINEX files. For a detail study of small TEC variations based on the initial dependence, the trend was removed by subtraction of the moving average with the use of the linear weight function. In the experiments radio path from GNSS satellite to Vasilsursk passed over the disturbed region of ionosphere, but radio paths to Zelenodolsk, to Kazan and to Yoshkar-Ola did not. However, TEC-variations correlated with pumping of ionosphere by ”Sura” facility were detected for three ground measurements sites, situated along the “Sura” facility geomagnetic longitude (Vasilsursk, Zelenodolsk, Kazan). Magnitudes of TEC-variations reached 0.15-0.3 TECU. Velocity of propagation of large-scale ionospheric disturbance stimulated by powerful radio wave along the geomagnetic latitude is about 320 m/s in the west-east direction. In connection with the above matter the found effect described in the report needs further detailed investigation and discussion. This work was supported by the Russian Foundation for Basic Research (grants No. 12-02-00513, 13-02-00957, 14-02-31459).

  1. Trace element emissions. Semi-annual report, October 1994--February 1995

    SciTech Connect

    Pigeaud, A.; Maru, H.; Wilemski, G.; Helble, J.

    1995-02-01

    Many trace elements can exist in raw coal gas either in the form of metallic vapors or gaseous compounds which, besides their action on potentially ``very clean`` advanced power generating systems such as fuel cells and gas turbines, can also be detrimental to plant and animal life when released into the atmosphere. Therefore, volatile trace contaminants from coal which can also be toxic must be removed before they become detrimental to both power plant performance/endurance and the environment. Five trace elements were selected in this project based on: abundance in solid coal, volatility during gasification, effects on downstream systems and toxicity to plant and animal life. An understanding was sought in this investigation of the interactions of these five trace elements (and their high temperature species) with the different components in integrated cleanup and power generating systems, as well as the ultimate effects with respect to atmospheric emissions. Utilizing thermodynamic calculations and various experimental techniques, it was determined that a number of trace contaminants that exist in coal may be substantially removed by flyash, and after that by different sorbent systems. High temperature cleanup of contaminants by sorbents such as zinc titanate, primarily to remove sulfur, can also absorb some metallic contaminants such as cadmium and antimony. Further polishing will be required, however, to eliminate trace contaminant species incorporating the elements arsenic, selemium, lead, and mercury.

  2. 2nd stage seed-cotton cleaning system total particulate emission factors and rates for cotton gins

    Technology Transfer Automated Retrieval System (TEKTRAN)

    This manuscript is part of a series of manuscripts that characterize cotton gin emissions from the standpoint of stack sampling. The impetus behind this project was the urgent need to collect additional cotton gin emissions data to address current regulatory issues. A key component of this study was...

  3. Emissions and Total Energy Consumption of a Multicylinder Piston Engine Running on Gasoline and a Hydrogen-gasoline Mixture

    NASA Technical Reports Server (NTRS)

    Cassidy, J. F.

    1977-01-01

    A multicylinder reciprocating engine was used to extend the efficient lean operating range of gasoline by adding hydrogen. Both bottled hydrogen and hydrogen produced by a research methanol steam reformer were used. These results were compared with results for all gasoline. A high-compression-ratio, displacement production engine was used. Apparent flame speed was used to describe the differences in emissions and performance. Therefore, engine emissions and performance, including apparent flame speed and energy lost to the cooling system and the exhaust gas, were measured over a range of equivalence ratios for each fuel. All emission levels decreased at the leaner conditions. Adding hydrogen significantly increased flame speed over all equivalence ratios.

  4. 40 CFR 98.83 - Calculating GHG emissions.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... (CONTINUED) MANDATORY GREENHOUSE GAS REPORTING Cement Production § 98.83 Calculating GHG emissions. You must...) and (b) of this section. (a) For each cement kiln that meets the conditions specified in § 98.33(b)(4... process emissions of CO2 from cement manufacturing, metric tons. CO2 Cli,m = Total annual emissions of...

  5. 40 CFR 98.83 - Calculating GHG emissions.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... (CONTINUED) MANDATORY GREENHOUSE GAS REPORTING Cement Production § 98.83 Calculating GHG emissions. You must...) and (b) of this section. (a) For each cement kiln that meets the conditions specified in § 98.33(b)(4... process emissions of CO2 from cement manufacturing, metric tons. CO2 Cli,m = Total annual emissions of...

  6. OBSERVABLE INDICATORS OF THE SENSITIVITY OF PM 2.5 NITRATE TO EMISSION REDUCTIONS, PART II: SENSITIVITY TO ERRORS IN TOTAL AMMONIA AND TOTAL NITRATE OF THE CMAQ-PREDICTED NONLINEAR EFFECT OF SO 2 EMISSION REDUCTIONS

    EPA Science Inventory

    The inorganic aerosol system of sulfate, nitrate, and ammonium can respond nonlinearly to changes in precursor sulfur dioxide (SO2) emissions. The potential increase in nitrate, when sulfate is reduced and the associated ammonia is released, can negate the sulfate mass...

  7. MEASUREMENT OF TOTAL SITE MERCURY EMISSIONS FROM A CHLOR-ALKALI PLANT USING OPEN-PATH UV-DOAS

    EPA Science Inventory

    In December 2003, the EPA promulgated the National Emission Standard for Hazardous Air Pollutants for mercury cell chlor-alkali plants. In February 2004, the Natural Resources Defense Council filed petitions on the final rule in U.S. district court citing, among other issues, th...

  8. OPTIMIZING MULTI-PHOTON FLUORESCENCE MICROSCOPY LIGHT COLLECTION FROM LIVING TISSUE BY NON-CONTACT TOTAL EMISSION DETECTION (epiTED)

    PubMed Central

    Combs, Christian A.; Smirnov, Aleksandr; Chess, David; McGavern, Dorian B.; Schroeder, James L.; Riley, Jason; Kang, Silvia S.; Lugar-Hammer, Merav; Gandjbakhche, Amir; Knutson, Jay R.; Balaban, Robert S.

    2012-01-01

    Summary A benefit of multiphoton fluorescence microscopy is the inherent optical sectioning that occurs during excitation at the diffraction-limited spot. The scanned collection of fluorescence emission is incoherent; i.e., no real image needs to be formed on the detector plane. The nearly isotropic emission of fluorescence excited at the focal spot allows for new detection schemes that efficiently funnel all attainable photons to detector(s). We previously showed (Combs et al., 2007) that parabolic mirrors and condensers could be combined to collect the totality of solid angle around the excitation spot for tissue blocks, leading to ~8-fold signal gain. Using a similar approach, we have developed an in vivo Total Emission Detection (epiTED) instrument modified to make non-contact images from outside of living tissue. Simulations suggest that a ~4 fold enhancement may be possible (much larger with lower NA objectives than the 0.95 NA used here) with this approach depending on objective characteristics, imaging depth and the characteristics of the sample being imaged. In our initial prototype, two fold improvements were demonstrated in the mouse brain and skeletal muscle as well as the rat kidney using a variety of fluorophores and no compromise of spatial resolution. These results show this epiTED effectively doubles emission signal in vivo ; thus, it will maintain the image signal to noise ratio (SNR) at two times the scan rate or enable full scan rate at approximately 30% reduced laser power (to minimize photo-damage). PMID:21118209

  9. Gradient anaysis of biomass in Costa Rica and a first estimate of total emissions of greenhouse gases from biomass burning

    SciTech Connect

    Helmer, E.H.; Brown, S.

    1997-12-31

    One important component of sustainable development for a nation is the degree to which it can balance greenhouse gas (GHG) exchange with the atmosphere. Scientists at NHEERL-WED recently estimated the release of such GHGs from the conversion of a range of forest types in Costa Rica between 1940-1983. They also evaluated the influence of environmental gradients that affect the rates and patterns of deforestation and the carbon pools of the forest cleared on GHG emissions.

  10. Annual dissolved nitrite plus nitrate and total phosphorous loads for the Susquehanna, St. Lawrence, Mississippi-Atchafalaya, and Columbia River basins, 1968-2004

    USGS Publications Warehouse

    Aulenbach, Brent T.

    2006-01-01

    Annual stream-water loads were calculated near the outlet of four of the larger river basins (Susquehanna, St. Lawrence, Mississippi-Atchafalaya, and Columbia) in the United States for dissolved nitrite plus nitrate (NO2 + NO3) and total phosphorus using LOADEST load estimation software. Loads were estimated for the period 1968-2004; although loads estimated for individual river basins and chemical constituent combinations typically were for shorter time periods due to limitations in data availability. Stream discharge and water-quality data for load estimates were obtained from the U.S. Geological Survey (USGS) with additional stream discharge data for the Mississippi-Atchafalaya River Basin from the U.S. Army Corps of Engineers. The loads were estimated to support national assessments of changes in stream nutrient loads that are periodically conducted by Federal agencies (for example, U.S. Environmental Protection Agency) and other water- and land-resource organizations. Data, methods, and results of load estimates are summarized herein; including World Wide Web links to electronic ASCII text files containing the raw data. The load estimates are compared to dissolved NO2 + NO3 loads for three of the large river basins from 1971 to 1998 that the USGS provided during 2001 to The H. John Heinz III Center for Science, Economics and the Environment (The Heinz Center) for a report The Heinz Center published during 2002. Differences in the load estimates are the result of using the most up-to-date monitoring data since the 2001 analysis, differences in how concentrations less than the reporting limit were handled by the load estimation models, and some errors and exclusions in the 2001 analysis datasets (which resulted in some inaccurate load estimates).

  11. Annual emissions of CH4 and N2O, and ecosystem respiration, from eight organic soils in Western Denmark managed by agriculture

    NASA Astrophysics Data System (ADS)

    Petersen, S. O.; Hoffmann, C. C.; Schäfer, C.-M.; Blicher-Mathiesen, G.; Elsgaard, L.; Kristensen, K.; Larsen, S. E.; Torp, S. B.; Greve, M. H.

    2012-01-01

    The use of organic soils by agriculture involves drainage and tillage, and the resulting increase in C and N turnover can significantly affect their greenhouse gas balance. This study estimated annual fluxes of CH4 and N2O, and ecosystem respiration (Reco), from eight organic soils managed by agriculture. The sites were located in three regions representing different landscape types and climatic conditions, and three land use categories were covered (arable crops, AR, grass in rotation, RG, and permanent grass, PG). The normal management at each site was followed, except that no N inputs occurred during the monitoring period from August 2008 to October 2009. The stratified sampling strategy further included six sampling points in three blocks at each site. Environmental variables (precipitation, PAR, air and soil temperature, soil moisture, groundwater level) were monitored continuously and during sampling campaigns, where also groundwater samples were taken for analysis. Gaseous fluxes were monitored on a three-weekly basis, giving 51, 49 and 38 field campaigns for land use categories AR, PG and RG, respectively. Climatic conditions in each region during monitoring were representative as compared to 20-yr averages. Peat layers were shallow, typically 0.5 to 1 m, and with a pH of 4 to 5. At six sites annual emissions of N2O were in the range 3 to 24 kg N2O-N ha-1, but at two arable sites (spring barley, potato) net emissions of 38 and 61 kg N2O-N ha-1 were recorded. The two high-emitting sites were characterized by fluctuating groundwater, low soil pH and elevated groundwater SO42- concentrations. Annual fluxes of CH4 were generally small, as expected, ranging from 2 to 4 kg CH4 ha-1. However, two permanent grasslands had tussocks of Juncus effusus L. (soft rush) in sampling points that were consistent sources of CH4 throughout the year. Emission factors for organic soils in rotation and with permanent grass, respectively, were estimated to be 0.011 and 0.47 g m-2 for CH4, and 2.5 and 0.5 g m-2 for N2O. This first documentation of CH4 and N2O emissions from managed organic soils in Denmark confirms the levels and wide ranges of emissions previously reported for the Nordic countries. However, the stratified experimental design also identified links between gaseous emissions and site-specific conditions with respect to soil, groundwater and vegetation which point to areas of future research that may account for part of the variability and hence lead to improved emission factors or models.

  12. Annual emissions of CH4 and N2O, and ecosystem respiration, from eight organic soils in Western Denmark managed by agriculture

    NASA Astrophysics Data System (ADS)

    Petersen, S. O.; Hoffmann, C. C.; Schäfer, C.-M.; Blicher-Mathiesen, G.; Elsgaard, L.; Kristensen, K.; Larsen, S. E.; Torp, S. B.; Greve, M. H.

    2011-10-01

    The use of organic soils by agriculture involves drainage and tillage, and the resulting increase in C and N turnover can significantly affect their greenhouse gas balance. This study estimated annual fluxes of CH4 and N2O, and ecosystem respiration (Reco), from eight organic soils managed by agriculture. The sites were located in three regions representing different landscape types and climatic conditions, and three land use categories (arable crops, AR, grass in rotation, RG, and permanent grass, PG) were covered. The normal management at each site was followed, except that no N inputs occurred during the monitoring period from August 2008 to October 2009. The stratified sampling strategy further included six sampling points in three blocks at each site. Environmental variables (precipitation, PAR, air and soil temperature, soil moisture, groundwater level) were monitored continuously and during sampling campaigns, where also groundwater samples were taken for analysis. Gaseous fluxes were monitored on a three-weekly basis, giving 51, 49 and 38 field campaigns for land use categories AR, PG and RG, respectively. Climatic conditions in each region during monitoring were representative based on 20-yr averages. Peat layers were shallow, typically 0.5 to 1 m, and with a pH of 4-5. At six sites annual emissions of N2O were in the range 3 to 24 kg N2O-N ha-1, but at two arable sites (spring barley, potato) net emissions of 38 and 61 kg N2O-N ha-1 were recorded. Both were characterized by fluctuating groundwater with elevated SO42- concentrations. Annual fluxes of CH4 were generally small, as expected, ranging from -2 to 4 kg CH4 ha-1. However, two permanent grasslands had tussocks of Juncus effusus (soft rush) in sampling points that were consistent sources of CH4 throughout the year. Emission factors for organic soils in rotation and permanent grass, respectively, were estimated to be 0.011 and 0.47 g m-2 for CH4, and 2.5 and 0.5 g m-2 for N2O. This first documentation of CH4 and N2O emissions from managed organic soils in Denmark confirms the levels and wide ranges of emissions previously reported for this region. However, the factorial approach also identified links between gaseous emissions and site-specific conditions with respect to soil, groundwater and vegetation which point to areas of future research that may account for part of the variability and hence lead to improved emission factors or models.

  13. Title V Semi-Annual Emissions Report for Permit P100R1 July 1, 2011 - December 31, 2011

    SciTech Connect

    Whetham, Walter

    2012-03-15

    Reports of actual emissions from permitted sources in Section 2.0 shall be submitted on a 6 month basis. Reports shall not include emissions from insignificant activities. Emission estimates of criteria pollutants NOx, CO, SO2, PM and VOCs shall not include fugitive emissions. Emission estimates of HAPs shall include fugitive emissions. The reports shall include a comparison of actual emissions that occurred during the reporting period with the facility-wide allowable emission limits specified in Section 2.11 of this permit. The report required by Condition 4.1 shall be submitted within 90 days from the end of the reporting period. The semiannual report required by Condition 4.2 shall be submitted within 45 days from the end of the reporting period. The reporting periods are January 1st to June 30th and July 1st to December 31st. This condition is pursuant to 20.2.70.302.E.1 NMAC.

  14. Radiative Transfer Models of Tidal Disruption Events: What Sets their Emission Line Strengths and Total Optical Flux?

    NASA Astrophysics Data System (ADS)

    Roth, Nathaniel; Kasen, Daniel; Guillochon, James; Ramirez-Ruiz, Enrico

    2016-01-01

    Given the recent influx of observational data and theoretical investigation into the nature of the tidal disruption of stars by super-massive black holes (TDEs), a full radiative transfer calculation applicable to an optically thick, electron scattering-dominated reprocessing region can provide valuable insight. Such a calculation can help address puzzles such as the lack of hydrogen emission lines in the optical spectra some TDEs, the origin of the optical and UV flux, and the simultaneous observation of x-rays along with the optical emission. In this talk I will discuss such a calculation performed with my collaborators as part of my dissertation. We track the reprocessing of accretion luminosity from a supermassive black hole as the light travels through an extended, spherical envelope composed of hydrogen, helium, and oxygen from the disrupted star. The steady-state radiative transfer equation is coupled to a solver for the atomic level populations and ionization states that does not assume local thermodynamic equilibrium. Our calculations show how the hydrogen optical emission lines can become more effectively optically thick than their helium counterparts, causing them to remain hidden even in the disruption of a hydrogen-rich star. More generally, variations in the structure of the reprocessing material can give rise to a variety of hydrogen-to-helium line ratios, as has been seen in recent observations. We also determine the amount of material necessary to transfer enough radiative energy from x-ray to optical wavelengths to match what is observed, and we demonstrate how the partial absorption of ionizing radiation can give rise to events simultaneously observed in x-rays and in the optical.

  15. RECOMMENDED OPERATING PROCEDURE NO. 2.3: SAMPLING AND ANALYSIS OF TOTAL HYDROCARBONS FROM SOURCES BY CONTINUOUS EMISSION MONITOR

    EPA Science Inventory

    The report is a recommended operating procedure (ROP) prepared for use in research activities conducted by EPA's Air and Energy Engineering Research Laboratory (AEERL). he described method is applicable to the continuous measurement of total hydrocarbons (THCs), also known as tot...

  16. Soil efflux and total emission rates of magmatic CO2 at the horseshoe lake tree kill, mammoth mountain, California, 1995-1999

    USGS Publications Warehouse

    Gerlach, T.M.; Doukas, M.P.; McGee, K.A.; Kessler, R.

    2001-01-01

    We report the results of eight soil CO2 efflux surveys by the closed circulation chamber method at the Horseshoe Lake tree kill (HLTK) - the largest tree kill on Mammoth Mountain. The surveys were undertaken from 1995 to 1999 to constrain total HLTK CO2 emissions and to evaluate occasional efflux surveys as a surveillance tool for the tree kills. HLTK effluxes range from 1 to > 10,000 g m -2 day -1 (grams CO2 per square meter per day); they are not normally distributed. Station efflux rates can vary by 7-35% during the course of the 8- to 16-h surveys. Disturbance of the upper 2 cm of ground surface causes effluxes to almost double. Semivariograms of efflux spatial covariance fit exponential or spherical models; they lack nugget effects. Efflux contour maps and total CO2 emission rates based on exponential, spherical, and linear kriging models of survey data are nearly identical; similar results are also obtained with triangulation models, suggesting that the kriging models are not seriously distorted by the lack of normal efflux distributions. In addition, model estimates of total CO2 emission rates are relatively insensitive to the measurement precision of the efflux rates and to the efflux value used to separate magmatic from forest soil sources of CO2. Surveys since 1997 indicate that, contrary to earlier speculations, a termination of elevated CO2 emissions at the HLTK is unlikely anytime soon. The HLTK CO2 efflux anomaly fluctuated greatly in size and intensity throughout the 1995-1999 surveys but maintained a N-S elongation, presumably reflecting fault control of CO2 transport from depth. Total CO2 emission rates also fluctuated greatly, ranging from 46 to 136 t day-1 (metric tons CO2 per day) and averaging 93 t day-1. The large inter-survey variations are caused primarily by external (meteorological) processes operating on time scales of hours to days. The externally caused variations can mask significant changes occurring at depth; a striking example is the masking of a degassing event generated at depth and detected by a soil gas sensor network in September 1997 while an efflux survey was in progress. Thus, occasional efflux surveys are not an altogether effective surveillance tool for the HLTK, and making them effective by greatly increasing their frequency may not be practical. Published by Elsevier Science B.V.

  17. Total prompt γ-ray emission in fission of U235, Pu239,241, and Cf252

    NASA Astrophysics Data System (ADS)

    Chyzh, A.; Wu, C. Y.; Kwan, E.; Henderson, R. A.; Bredeweg, T. A.; Haight, R. C.; Hayes-Sterbenz, A. C.; Lee, H. Y.; O'Donnell, J. M.; Ullmann, J. L.

    2014-07-01

    The total prompt γ-ray energy distributions for the neutron-induced fission of U235 and Pu239,241 in the neutron energy range of 0.025 eV - 100 keV and the spontaneous fission of Cf252 were measured using the Detector for Advanced Neutron Capture Experiments (DANCE) in coincidence with the detection of fission fragments by a parallel-plate avalanche counter. DANCE is a highly segmented, highly efficient 4π γ-ray calorimeter. Corrections were made to the measured distribution by unfolding the two-dimension spectrum of total γ-ray energy vs multiplicity using a simulated DANCE response matrix generated with a geometrical model of the detector arrays and validated with the γ-ray calibration sources. The mean values of the total prompt γ-ray energy, determined from the unfolded distributions, are ˜20% higher than those of early measurements for all the fissile nuclei studied. The implication for the γ heating in nuclear reactors is discussed.

  18. Yearly variation and annual cycle of total column ozone over New Delhi (29°N, 77°E), India and Halley Bay (76°S, 27°W), British Antarctic Survey Station and its effect on night airglow intensity of OH(8, 3) for the period 1979-2005

    NASA Astrophysics Data System (ADS)

    Jana, P. K.; Saha, D. K.; Sarkar, D.

    2012-12-01

    A critical analysis made on the long-term monthly, seasonal, yearly variation and annual cycle of total column ozone (TCO) concentration at New Delhi (29°N, 77°E), India and Halley Bay (76°S, 27°W), a British Antarctic Service Station reveals more decline in yearly mean ozone concentration at Halley Bay than at New Delhi from 1979 to 2005. The nature of variations of monthly mean TCO during the months of August and September was the most identical with that of yearly mean ozone values at New Delhi and Halley Bay, respectively, for the same period. Annual cycles of TCO over these stations are completely different for the above period. The effect of O3 depletion on night airglow emission of OH(8, 3) line at New Delhi and Halley Bay has been studied. Calculations based on chemical kinetics show that the airglow intensity of OH(8, 3) has also been affected due to the depletion of O3 concentration. The yearly variations and annual cycle of intensities of OH(8, 3) line for the above two stations are depicted and compared. It has been shown that the rate of decrease of intensity of OH(8, 3) line was comparatively more at Halley Bay due to dramatic decrease of Antarctic O3 concentration.

  19. Determination of free and total sulfur dioxide in wine samples by vapour-generation inductively coupled plasma-optical-emission spectrometry.

    PubMed

    Cmelík, Jirí; Machát, Jirí; Niedobová, Eva; Otruba, Vítezslav; Kanický, Viktor

    2005-10-01

    Sulfur dioxide (SO(2)) is used as a preservative and stabilizer in wine production to prevent undesired biochemical processes in the must and the final product. The concentration of SO(2) is restricted by national regulations. There are two main forms of SO(2) in wine-free (inorganic forms) and bound (fixed to organic compounds, e.g. aldehydes). Iodometric titration is commonly employed for determination of SO(2) concentration (either by direct titration or after pre-separation by distillation); other techniques are also used. In this work inductively coupled plasma-optical-emission spectrometry with vapour generation was used for determination of free and total SO(2) in wine. Gaseous SO(2) is released from the sample by addition of acid and swept into the ICP by an argon stream. The intensity of the sulfur atomic emission lines is measured in the vacuum UV region. Determination of total SO(2) is performed after hydrolysis of bound forms with sodium hydroxide (NaOH). Concentrations of acid for vapour generation and NaOH for hydrolysis were optimised. The method was used for determination of free and total SO(2) in red and white wine samples and results were compared with those from iodometric titration. PMID:16052345

  20. Prescribed-burning vs. wildfire: management implications for annual carbon emissions along a latitudinal gradient of Calluna vulgaris-dominated vegetation

    NASA Astrophysics Data System (ADS)

    Santana, V. M.; Alday, J. G.; Lee, H.; Allen, K. A.; Marrs, R. H.

    2015-11-01

    A~present challenge in fire ecology is to optimize management techniques so that ecological services are maximized and C emissions minimized. Here, we model the effects of different prescribed-burning rotation intervals and wildfires on carbon emissions (present and future) in British moorlands. Biomass-accumulation curves from four Calluna-dominated ecosystems along a north-south, climatic gradient in Great Britain were calculated and used within a matrix-model based on Markov Chains to calculate above-ground biomass-loads, and annual C losses under different prescribed-burning rotation intervals. Additionally, we assessed the interaction of these parameters with an increasing wildfire return interval. We observed that litter accumulation patterns varied along the latitudinal gradient, with differences between northern (colder and wetter) and southern sites (hotter and drier). The accumulation patterns of the living vegetation dominated by Calluna were determined by site-specific conditions. The optimal prescribed-burning rotation interval for minimizing annual carbon losses also differed between sites: the rotation interval for northern sites was between 30 and 50 years, whereas for southern sites a hump-backed relationship was found with the optimal interval either between 8 to 10 years or between 30 to 50 years. Increasing wildfire frequency interacted with prescribed-burning rotation intervals by both increasing C emissions and modifying the optimum prescribed-burning interval for C minimum emission. This highlights the importance of studying site-specific biomass accumulation patterns with respect to environmental conditions for identifying suitable fire-rotation intervals to minimize C losses.

  1. Anthropogenic chromium emissions in china from 1990 to 2009.

    PubMed

    Cheng, Hongguang; Zhou, Tan; Li, Qian; Lu, Lu; Lin, Chunye

    2014-01-01

    An inventory of chromium emission into the atmosphere and water from anthropogenic activities in China was compiled for 1990 through to 2009. We estimate that the total emission of chromium to the atmosphere is about 1.92×10⁵ t. Coal and oil combustion were the two leading sources of chromium emission to the atmosphere in China, while the contribution of them showed opposite annual growth trend. In total, nearly 1.34×10⁴ t of chromium was discharged to water, mainly from six industrial categories in 20 years. Among them, the metal fabrication industry and the leather tanning sector were the dominant sources of chromium emissions, accounting for approximately 68.0% and 20.0% of the total emissions and representing increases of 15.6% and 10.3% annually, respectively. The spatial trends of Cr emissions show significant variation based on emissions from 2005 to 2009. The emission to the atmosphere was heaviest in Hebei, Shandong, Guangdong, Zhejiang and Shanxi, whose annual emissions reached more than 1000t for the high level of coal and oil consumption. In terms of emission to water, the largest contributors were Guangdong, Jiangsu, Shandong and Zhejiang, where most of the leather production and metal manufacturing occur and these four regions accounted for nearly 47.4% of the total emission to water. PMID:24505309

  2. Anthropogenic Chromium Emissions in China from 1990 to 2009

    PubMed Central

    Cheng, Hongguang; Zhou, Tan; Li, Qian; Lu, Lu; Lin, Chunye

    2014-01-01

    An inventory of chromium emission into the atmosphere and water from anthropogenic activities in China was compiled for 1990 through to 2009. We estimate that the total emission of chromium to the atmosphere is about 1.92×105t. Coal and oil combustion were the two leading sources of chromium emission to the atmosphere in China, while the contribution of them showed opposite annual growth trend. In total, nearly 1.34×104t of chromium was discharged to water, mainly from six industrial categories in 20 years. Among them, the metal fabrication industry and the leather tanning sector were the dominant sources of chromium emissions, accounting for approximately 68.0% and 20.0% of the total emissions and representing increases of15.6% and 10.3% annually, respectively. The spatial trends of Cr emissions show significant variation based on emissions from 2005 to 2009. The emission to the atmosphere was heaviest in Hebei, Shandong, Guangdong, Zhejiang and Shanxi, whose annual emissions reached more than 1000t for the high level of coal and oil consumption. In terms of emission to water, the largest contributors were Guangdong, Jiangsu, Shandong and Zhejiang, where most of the leather production and metal manufacturing occur and these four regions accounted for nearly 47.4% of the total emission to water. PMID:24505309

  3. 17 CFR 270.30b1-2 - Semi-annual report for totally-owned registered management investment company subsidiary of...

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ...-owned registered management investment company subsidiary of registered management investment company...-owned registered management investment company subsidiary of registered management investment company... subsidiary of a registered management investment company need not file a semi-annual report on Form N-SAR...

  4. Measurements of Total Hemispherical Emissivity of Several Stably Oxidized Nickel-Titanium Carbide Cemented Hard Metals from 600 F to 1,600 F

    NASA Technical Reports Server (NTRS)

    Wade, William R.; Casey, F. W., Jr.

    1959-01-01

    The total hemispherical emissivity of several nickel-titanium carbide cemented hard metals have been measured over a temperature range from 600 F to l,600 F. A variety of cemented hard metals were obtained from the Kennametal Corporation. A brief discussion of the apparatus employed and the procedures used for this investigation is included. The results of the tests of specimens in the as-received and polished states indicate a nearly constant emissivity for each material tested over the temperature range considered and only slight differences in emissivity values for the different materials. Values obtained on the stably oxidized specimens range from 0.90 to 0.94 at 6000 F and o.88 to 0.92 at 1,600 F for the as-received specimens and from 0.82 to 0.89 at 600 F and 0.85 to 0.87 at 1,600 F for the polished specimens. The surface analysis of the oxidized materials as obtained by X-ray diffraction methods and metallographic techniques are presented as an aid to reproducing the surface on which these measurements were made.

  5. Development of particle induced gamma-ray emission methods for nondestructive determination of isotopic composition of boron and its total concentration in natural and enriched samples.

    PubMed

    Chhillar, Sumit; Acharya, Raghunath; Sodaye, Suparna; Pujari, Pradeep K

    2014-11-18

    We report simple particle induced gamma-ray emission (PIGE) methods using a 4 MeV proton beam for simultaneous and nondestructive determination of the isotopic composition of boron ((10)B/(11)B atom ratio) and total boron concentrations in various solid samples with natural isotopic composition and enriched with (10)B. It involves measurement of prompt gamma-rays at 429, 718, and 2125 keV from (10)B(p,αγ)(7)Be, (10)B(p, p'γ)(10)B, and (11)B(p, p'γ)(11)B reactions, respectively. The isotopic composition of boron in natural and enriched samples was determined by comparing peak area ratios corresponding to (10)B and (11)B of samples to natural boric acid standard. An in situ current normalized PIGE method, using F or Al, was standardized for total B concentration determination. The methods were validated by analyzing stoichiometric boron compounds and applied to samples such as boron carbide, boric acid, carborane, and borosilicate glass. Isotopic compositions of boron in the range of 0.247-2.0 corresponding to (10)B in the range of 19.8-67.0 atom % and total B concentrations in the range of 5-78 wt % were determined. It has been demonstrated that PIGE offers a simple and alternate method for total boron as well as isotopic composition determination in boron based solid samples, including neutron absorbers that are important in nuclear technology. PMID:25312472

  6. 40 CFR 98.33 - Calculating GHG emissions.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... chapter, as described in paragraph (a)(5) of this section. For units that combust both biomass and fossil fuels, you must calculate and report CO2 emissions from the combustion of biomass separately using the... quarterly totals are summed to determine the annual CO2 mass emissions. (vii) If both biomass and...

  7. The Wildland Fire Emission Inventory: emission estimates and an evaluation of uncertainty

    NASA Astrophysics Data System (ADS)

    Urbanski, S. P.; Hao, W. M.; Nordgren, B.

    2011-08-01

    We present the Wildland Fire Emission Inventory (WFEI), a high resolution model for non-agricultural open biomass burning (hereafter referred to as wildland fires) in the contiguous United States (CONUS). WFEI was used to estimate emissions of CO and PM2.5 for the western United States from 2003-2008. The estimated annual CO emitted ranged from 436 Gg yr-1 in 2004 to 3107 Gg yr-1 in 2007. The extremes in estimated annual PM2.5 emitted were 65 Gg yr-1 in 2004 and 454 Gg yr-1 in 2007. Annual wildland fire emissions were significant compared to other emission sources in the western United States as estimated in a national emission inventory. In the peak fire year of 2007, fire emissions were ~20 % of total CO emissions and ~39 % of total PM2.5 emissions. During the months with the greatest fire activity, wildland fires accounted for the majority of CO and PM2.5 emitted across the study region. The uncertainty in the inventory estimates of CO and PM2.5 emissions (ECO and EPM2.5, respectively) have been quantified across spatial and temporal scales relevant to regional and global modeling applications. The uncertainty in annual, domain wide emissions was 28 % to 51 % for CO and 40 % to 65 % for PM2.5. Sensitivity of the uncertainty in ECO and EPM2.5 to the emission model components depended on scale. At scales relevant to regional modeling applications (Δx = 10 km, Δt = 1 day) WFEI estimates 50 % of total ECO with an uncertainty <133 % and half of total EPM2.5 with an uncertainty <146 %. The uncertainty in ECO and EPM2.5 is significantly reduced at the scale of global modeling applications (Δx = 100 km, Δt = 30 day). Fifty percent of total emissions are estimated with an uncertainty <50 % for CO and <64 % for PM2.5. Uncertainty in the burned area drives the emission uncertainties at regional scales. At global scales the uncertainty in ECO is most sensitive to uncertainties in the fuel load consumed while the uncertainty in the emission factor for PM2.5 drives the EPM2.5 uncertainty. Our uncertainty analysis indicates that the large scale aggregate uncertainties (e.g. annual, CONUS) that are typically reported for biomass burning emission inventories may not be appropriate for evaluating and interpreting results of modeling applications that employ the emission estimates. When feasible, biomass burning emission inventories should be evaluated and reported across the scales for which they are intended to be used.

  8. Soil concentration profiles and diffusion and emission of nitrous oxide influenced by the application of biochar in a rice-wheat annual rotation system.

    PubMed

    Zhou, Ziqiang; Xu, Xin; Bi, Zhichao; Li, Lu; Li, Bo; Xiong, Zhengqin

    2016-04-01

    Field experiments were carried out to determine biochar effects on nitrous oxide (N2O) concentration profiles, diffusion, and emissions in paddy soil under rice-wheat annual rotation in southeastern China. An in situ soil gas device was adapted to measure N2O concentrations at depths of 7, 15, 30, and 50 cm. Five treatments were installed as N0B0, N0B1, N1B0, N1B1, and N1B2 (B0, B1, and B2 designated as biochar at 0, 20, and 40 t ha(-1), respectively, while N0 and N1 as nitrogen at 0 and 250 kg N ha(-1) crop(-1), respectively). The results showed that N2O concentrations were higher in the 15 and 30 cm depths than other depths. With positive diffusive fluxes, the 7 cm in the rice season and 15 cm in the wheat season were main production sites. The surface N2O emissions and topsoil diffusive fluxes showed good agreement. N application strongly increased soil N2O profiles and surface emissions. Relative to N1B0, N1B1 decreased N2O concentration, surface emissions, and diffusive fluxes by 25.2, 31.8, and 26.5 %, respectively, while N1B2 decreased them averagely by 40.7, 43.2, and 44.2 %, correspondingly. Therefore, the gas gradient method is effective for estimating N2O emissions, and biochar can decrease N2O production when N was applied. PMID:26769480

  9. Emission of polycyclic aromatic hydrocarbons in China

    SciTech Connect

    Shanshan Xu; Wenxin Liu; Shu Tao

    2006-02-01

    Emission of 16 polycyclic aromatic hydrocarbons (PAHs) listed as U.S. Environmental Protection Agency (U.S. EPA) priority pollutants from major sources in China were compiled. Geographical distribution and temporal change of the PAH emission, as well as emission profiles, are discussed. It was estimated that the total PAH emission in China was 25,300 tons in 2003. The emission profile featured a relatively higher portion of high molecular weight (HMW) species with carcinogenic potential due to large contributions of domestic coal and coking industry. Among various sources, biomass burning, domestic coal combustion, and the coking industry contributed 60%, 20%, and 16% of the total emission, respectively. Total emission, emission density, emission intensity, and emission per capita showed geographical variations. In general, the southeastern provinces were characterized by higher emission density, while those in western and northern China featured higher emission intensity and population-normalized emission. Although energy consumption in China went up continuously during the past two decades, annual emission of PAHs fluctuated depending on the amount of domestic coal consumption, coke production, and the efficiency of energy utilization. 47 refs., 6 figs.

  10. Intra- and inter-annual variability of VOC emissions from natural and semi-natural vegetation in Europe and neighbouring countries

    NASA Astrophysics Data System (ADS)

    Steinbrecher, Rainer; Smiatek, Gerhard; Köble, Renate; Seufert, Günther; Theloke, Jochen; Hauff, Karin; Ciccioli, Paolo; Vautard, Robert; Curci, Gabriele

    Biogenic VOC emission estimates from the earth's surface are crucial input parameters in air quality models. Knowledge accumulated in the last years about BVOC source distributions and chemical compound species emission profiles in Europe as well as the demand of air quality modellers for a finer resolution in space and time of BVOC estimates have led to the set-up of new emission modelling systems. An updated fast BVOC emission modelling platform explicitly considering the seasonality of emission potentials and leaf temperature gradients in forest canopies by the semi-empirical emission module (seBVOC) will be proposed and used for estimating hourly values of chemical compound-specific emissions in Europe (33-68° north; 10° west to 40° east) in the years 1997, 2000, 2001, and 2003. Spatial resolution will be 10 km by 10 km. The database used contains latest land and forest distributions, updated foliar biomass densities, leaf area indices (LAI), and plant as well as chemical compound-specific emission potentials, if available. Meteorological input parameters for the respective years will be generated using the non-hydrostatic meteorological model MM5. Highest BVOC emissions occur in daytime hours around noon from the end of May to mid-August in the Mediterranean area and from the mid of June to the end of July in the boreal forests. Comparison of 3 BVOC model approaches will reveal that for July 2003, the European isoprene and monoterpene totals range from 1124 Gg to 1446 Gg and from 338 Gg to 1112 Gg, respectively. Small-scale deviations may be as high as ±0.6 Mg km -2 for July 2003, reflecting the current uncertainty range for BVOC estimates. Key sources of errors in inventories are still insufficiently detailed land use data for some areas and lacking chemically speciated plant-specific emission potentials in particular in boreal, south-eastern, and northern African landscapes. The hourly emissions of isoprene, speciated terpenes, and oxyVOC have been made available by the NatAir database.

  11. DEVELOPMENT OF CRITERIA FOR EXTENSION OF APPLICABILITY OF LOW EMISSION, HIGH EFFICIENCY COAL BURNERS: SECOND ANNUAL REPORT

    EPA Science Inventory

    The report, describing the second year's effort under this contract, concerns the development of criteria for the evaluation and applicability of low-emission, high efficiency coal burners. The report describes progress in three major areas: (1) bench scale studies, (2) distribut...

  12. DEVELOPMENT OF CRITERIA FOR EXTENSION OF APPLICABILITY OF LOW-EMISSION, HIGH-EFFICIENCY COAL BURNERS: FOURTH ANNUAL REPORT

    EPA Science Inventory

    The report summarizes technical progress during the fourth year of effort on EPA contract 68-02-2667. NOx and SOx emission characteristics of two low-NOx distributed-mixing burners were tested with three coals in a large water-tube simulator furnace (50-70 million Btu/hr firing r...

  13. LLNL NESHAPs 2004 Annual Report

    SciTech Connect

    Harrach, R; Gallegos, G; Peterson, R; Wilson, K; Harrach, R J; Gallegos, G M; Peterson, S R; Wilson, K R

    2005-06-27

    This annual report is prepared pursuant to the National Emission Standards for Hazardous Air Pollutants (NESHAPs; Title 40 Code of Federal Regulations [CFR] Part 61, Subpart H). Subpart H governs radionuclide emissions to air from Department of Energy (DOE) facilities.

  14. Estimation of mercury emission from different sources to atmosphere in Chongqing, China.

    PubMed

    Wang, Dingyong; He, Lei; Wei, Shiqiang; Feng, Xinbin

    2006-08-01

    This investigation presents a first assessment of the contribution to the regional mercury budget from anthropogenic and natural sources in Chongqing, an important industrial region in southwest China. The emissions of mercury to atmosphere from anthropogenic sources in the region were estimated through indirect approaches, i.e. using commonly acceptable emission factors method, which based on annual process throughputs or consumption for these sources. The natural mercury emissions were estimated from selected natural sources by the dynamic flux chamber technique. The results indicated that the anthropogenic mercury emissions totaled approximately 8.85 tons (t), more than 50% of this total originated in coal combustion and 23.7% of this total emission in the industrial process (include cement production, metal smelting and chemical industry). The natural emissions represented approximately 17% of total emissions (1.78 t yr(-1)). The total mercury emission to atmosphere in Chongqing in 2001 was 10.63 t. PMID:16219340

  15. Total Quality Leadership

    NASA Technical Reports Server (NTRS)

    1991-01-01

    More than 750 NASA, government, contractor, and academic representatives attended the Seventh Annual NASA/Contractors Conference on Quality and Productivity. The panel presentations and Keynote speeches revolving around the theme of total quality leadership provided a solid base of understanding of the importance, benefits, and principles of total quality management (TQM). The presentations from the conference are summarized.

  16. Development of advanced electrochemical emission spectroscopy for monitoring corrosion in simulated DOE liquid waste. 1998 annual progress report

    SciTech Connect

    MacDonald, D.D.

    1998-06-01

    'Objective of this project is to develop and use Electrochemical Emission Spectroscopy (EES) and other electrochemical techniques as in situ tools for exploring corrosion mechanisms of iron and carbon steel in highly alkaline solutions and for continuously monitoring corrosion on structural materials in DOE liquid waste storage system. In particular, the author will explore the fundamental aspects of the passive behavior of pure iron since breakdown of passivity leads to localized corrosion. This report summarizes work after 1 year of a 3 year project.'

  17. IN ROW AND BETWEEN ROW ZONE HERBICIDE APPLICATION AT DIFFERENT RATES CONTROLS ANNUAL WEEDS AND REDUCES TOTAL RESIDUAL HERBICIDE USE IN CORN (ZEA MAYS)

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Zone herbicide application uses 1) crop management to enhance crop competitiveness with weeds, 2) soil residual herbicide banded over crop rows at reduced rates and 3) the same herbicide banded between rows at higher rates than over crop rows, so that total herbicide use per unit area is reduced. T...

  18. Total sulfur determination in gasoline, kerosene and diesel fuel using inductively coupled plasma optical emission spectrometry after direct sample introduction as detergent emulsions

    NASA Astrophysics Data System (ADS)

    Santelli, Ricardo Erthal; Oliveira, Eliane Padua; de Carvalho, Maria de Fátima Batista; Bezerra, Marcos Almeida; Freire, Aline Soares

    2008-07-01

    Herein, we present the development of a procedure for the determination of total sulfur in petroleum-derived products (gasoline, kerosene and diesel fuel) employing inductively coupled plasma optical emission spectrometry (ICP OES). For this procedure, samples were prepared as emulsions that were made using concentrated nitric acid, Triton X-100, sample, and ultra pure water in proportions of 5/10/7/78% (v/v), respectively. Sample volumes were weighed because of the density differences, and oxygen was added to the sheat gas entrance of the ICP OES in order to decrease carbon deposition in the torch and to minimize background effects. A Doehlert design was applied as an experimental matrix to investigate the flow ratios of argon (sheat and plasma gas) and oxygen in relation to the signal-to-background ratio. A comparative study among the slopes of the analytical curves built in aqueous media, surfactant/HNO 3, and by spike addition for several sample emulsions indicates that a unique solution of surfactant in acidic media can be employed to perform the external calibration for analysis of the emulsions. The developed procedure allows for the determination of the total sulfur content in petroleum derivatives with a limit of detection (LOD) and limit of quantification (LOQ) of 0.72 and 2.4 μg g - 1 , respectively. Precision values, expressed as the relative standard deviations (% RSD, n = 10) for 12 and 400 μg g - 1 , were 2.2% and 1.3%, respectively. The proposed procedure was applied toward the determination of total sulfur in samples of gasoline, kerosene, and diesel fuel commercialized in the city of Niterói/RJ, Brazil. The accuracy of the proposed method was evaluated by the determination of the total sulfur in three different standard reference materials (SRM): NIST 2723a (sulfur in diesel fuel oil), NIST 1616b (sulfur in kerosene), and NIST 2298 (sulfur in gasoline). The data indicate that the methodology can be successfully applied to these types of samples. Spiking tests, conducted with the analyzed samples, indicate that recoveries are between 97 and 103%.

  19. Contributions of the pollutant emission in South Korea to the aerosol concentrations and depositions in Asia

    NASA Astrophysics Data System (ADS)

    Park, Soon-Ung; Lee, In-Hye; Choe, Anna; Joo, Seung Jin

    2015-05-01

    The spatial distributions of annual mean concentrations and the annual total depositions of the Asian dust (AD) aerosol and the anthropogenic aerosol (AA) in 2010 are investigated with pollutant emissions over the whole model domain of Asia and without the pollutant emission from South Korea using the Aerosol Modeling System (AMS) that is modified from the Asian Dust Aerosol Model2 (ADAM2) and the Community Multi-Scale Air Quality (CMAQ) modeling System. The annual mean surface aerosol concentrations in Asia are found to affect a wide region as a complex mixture of AA and AD aerosols. However, the contribution of the pollutant emission from South Korea is found to be limited to the neighboring regions. The annual total aerosol deposition in Asia is 485.2 Tg. However, the contribution due to the pollutant emission from South Korea is about 1.9 Tg, suggesting of no significant contribution to the environment.

  20. Prediction of BOD, COD, and Total Nitrogen Concentrations in a Typical Urban River Using a Fluorescence Excitation-Emission Matrix with PARAFAC and UV Absorption Indices

    PubMed Central

    Hur, Jin; Cho, Jinwoo

    2012-01-01

    The development of a real-time monitoring tool for the estimation of water quality is essential for efficient management of river pollution in urban areas. The Gap River in Korea is a typical urban river, which is affected by the effluent of a wastewater treatment plant (WWTP) and various anthropogenic activities. In this study, fluorescence excitation-emission matrices (EEM) with parallel factor analysis (PARAFAC) and UV absorption values at 220 nm and 254 nm were applied to evaluate the estimation capabilities for biochemical oxygen demand (BOD), chemical oxygen demand (COD), and total nitrogen (TN) concentrations of the river samples. Three components were successfully identified by the PARAFAC modeling from the fluorescence EEM data, in which each fluorophore group represents microbial humic-like (C1), terrestrial humic-like organic substances (C2), and protein-like organic substances (C3), and UV absorption indices (UV220 and UV254), and the score values of the three PARAFAC components were selected as the estimation parameters for the nitrogen and the organic pollution of the river samples. Among the selected indices, UV220, C3 and C1 exhibited the highest correlation coefficients with BOD, COD, and TN concentrations, respectively. Multiple regression analysis using UV220 and C3 demonstrated the enhancement of the prediction capability for TN. PMID:22368505

  1. Prediction of BOD, COD, and total nitrogen concentrations in a typical urban river using a fluorescence excitation-emission matrix with PARAFAC and UV absorption indices.

    PubMed

    Hur, Jin; Cho, Jinwoo

    2012-01-01

    The development of a real-time monitoring tool for the estimation of water quality is essential for efficient management of river pollution in urban areas. The Gap River in Korea is a typical urban river, which is affected by the effluent of a wastewater treatment plant (WWTP) and various anthropogenic activities. In this study, fluorescence excitation-emission matrices (EEM) with parallel factor analysis (PARAFAC) and UV absorption values at 220 nm and 254 nm were applied to evaluate the estimation capabilities for biochemical oxygen demand (BOD), chemical oxygen demand (COD), and total nitrogen (TN) concentrations of the river samples. Three components were successfully identified by the PARAFAC modeling from the fluorescence EEM data, in which each fluorophore group represents microbial humic-like (C1), terrestrial humic-like organic substances (C2), and protein-like organic substances (C3), and UV absorption indices (UV(220) and UV(254)), and the score values of the three PARAFAC components were selected as the estimation parameters for the nitrogen and the organic pollution of the river samples. Among the selected indices, UV(220), C3 and C1 exhibited the highest correlation coefficients with BOD, COD, and TN concentrations, respectively. Multiple regression analysis using UV(220) and C3 demonstrated the enhancement of the prediction capability for TN. PMID:22368505

  2. The measurement of the ionospheric total content variations caused by a powerful radio emission of "Sura" facility on a network of GNSS-receivers

    NASA Astrophysics Data System (ADS)

    Nasyrov, I. A.; Kogogin, D. A.; Shindin, A. V.; Grach, S. M.; Zagretdinov, R. V.

    2016-02-01

    Observations of the perturbations of total electron content (TEC) caused by a powerful radio emission of "Sura" facility (Radio Physical Research Institute, N. Novgorod) were carried out during several experimental campaigns from March of 2010 to March 2013. In this paper the data of experimental measurements of TEC-variations conducted on March, 15, 2010 and on March, 12, 2013, are presented. Parameters of TEC-variations were obtained by dual-frequency global navigation satellite systems (GNSS) diagnostics. Registration of signal parameters from GNSS-transmitters was performed at spatially separated sites along the geomagnetic latitude: Vasilsursk (56 °08‧ N, 46 °05‧ E), Zelenodolsk (55 °52‧ N, 48 °33‧ E) and Kazan (55 °48‧ N, 49 °08‧ E). In the experiments radio path from GNSS satellite to Vasilsursk passed over the disturbed region of ionosphere, but radio paths to Zelenodolsk and to Kazan did not. However, TEC-variations correlated with pumping of ionosphere by "Sura" facility were detected for all up to three ground measurements sites. Magnitudes of TEC-variations reached up to ∼ 0.6 - 0.7 TECU. The speculation that a sharp gradient of the electron density formed at the border of the main lobe of "Sura" facility may cause the generation of IGW is presented.

  3. Branch-level measurement of total OH reactivity for constraining unknown BVOC emission during the CABINEX (Community Atmosphere-Biosphere INteractions Experiments)-09 Field Campaign

    NASA Astrophysics Data System (ADS)

    Kim, S.; Guenther, A.; Karl, T.; Greenberg, J.

    2011-03-01

    We present OH reactivity measurements using the comparative reactivity method with a branch enclosure technique for four different tree species (red oak, white pine, beech and red maple) in the UMBS PROPHET tower footprint during the Community Atmosphere Biosphere INteraction EXperiment (CABINEX) field campaign in July of 2009. Proton Transfer Reaction-Mass Spectrometry (PTR-MS) was sequentially used as a detector for OH reactivity and BVOC including isoprene and monoterpenes (MT), in enclosure air, so that the measurement dataset contains both measured OH reactivity and calculated OH reactivity from well-known BVOC. The results indicate that isoprene and MT, and in one case a sesquiterpene, can account for the measured OH reactivity. Significant discrepancy between measured OH reactivity and calculated OH reactivity from isoprene and MT is found for the red maple enclosure dataset but it can be reconciled by adding reactivity from emission of a sesquiterpene, α-farnesene, detected by GC-MS. This leads us to conclude that no significant unknown BVOC emission contributed to ambient OH reactivity from these trees at least during the study period. This conclusion leads us to explore the contribution from unmeasured isoprene (the dominant OH sink in this ecosystem) oxidation products such as hydroxyacetone, glyoxal, methylglyoxal and C4 and C5-hydroxycarbonyl using recently published isoprene oxidation mechanisms (Mainz Isoprene Mechanism II and Leuven Isoprene Mechanism). Evaluation of conventionally unmeasured first generation oxidation products of isoprene and their possible contribution to ambient missing OH reactivity indicates that the ratio of OH reactivity from unmeasured products over OH reactivity from MVK + MACR is strongly dependent on NO concentrations. The unmeasured oxidation products can contribute ~7.2% (8.8% from LIM and 5.6% by MIM 2 when NO = 100 pptv) of the isoprene contribution towards total ambient OH reactivity. This amount can explain ~8.0% (9.7% from LIM and 6.2% from MIM 2) of missing OH reactivity, reported by Di Carlo et al. (2004) at the same site. Further study on contribution from further generation of unmeasured oxidation products should be followed to constrain tropospheric photochemical reactivity of BVOC that have important implications for both photochemical ozone and secondary organic aerosol formation.

  4. Biogenic voc emissions development and its impacts on regional o3 in PRD, china

    NASA Astrophysics Data System (ADS)

    Wang, Xuemei; Shuping, Situ; Guenther, Alex; Chen, Fei; Wu, Zhiyong

    2010-05-01

    The new Model of Emissions of Gases and Aerosols from Nature (MEGAN) has been coupled with WRF-Chem to investigate the influence of biogenic violate organic carbon (BVOC ) emissions on the regional distribution of O3 and SOA concentration in the Pearl River Delta (PRD), China. MEGAN first estimate an emission factor which represents the net above-canopy emission rate expected at optimal conditions, and use a number of environmental correction factor based on photosynthetically activated radiation (PAR) and leaf temperature to adjust the emission rate due to deviations from optimal conditions. Total emissions are the sum of emissions estimated for each plant functional type (PFT) in a given grid cell. Our model simulations estimated showed: (1) Total annual BVOCs emissions were 339.01× 106 kg, which is 40.68% of annual AVOCs emissions and 28.91% of total VOCs emission in PRD in 2006. Isoprene, monoterpene, sesquiterpene and OVOCs contributed about 31.94%, 39.23%, 3.27% and 25.56% of the estimated total annual emissions respectively. α- pinene and β- pinene were the major components in monoterpene, which contributed 28.09% and 26.98% to the total annual monoterpene emissions respectively;β-caryophyllene andα-farnesene were two important sesquiterpene, and they contributed to 22.31% and 18.76% of the annual sesquiterpene emissions.(2) BVOCs emissions have large variations in their spatial distributions, which were mainly resulted from the differences in the geographical distribution of vegetation. Their emission amounts were larger in the places where urbanization were relative lower and plants distributions were higher.(3) Emissions of terpenoids had significant annual and diurnal variations and the largest emission rate occurred at 13:00 local time while the amount of emission in summer is the largest.(4) There were significant terpenoids emission rate (≥1.21.2 kg km-2h-1) in the remote areas in PRD region where the emissions of AVOCs were low, and terpenoids may control the air quality especially the ozone formation in those areas.WRF-Chem-MEGAN model will be used to investigate the impacts of BVOC on regional ozone concentration in PRD.

  5. 40 CFR 86.166-12 - Method for calculating emissions due to air conditioning leakage.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... determine a refrigerant leakage rate in grams per year from vehicle-based air conditioning units. The...). (a) Emission totals. Calculate an annual rate of refrigerant leakage from an air conditioning system... described in paragraph (b) of this section. Grams/YRSP = Emission rate for service ports and...

  6. 40 CFR 86.166-12 - Method for calculating emissions due to air conditioning leakage.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... determine a refrigerant leakage rate in grams per year from vehicle-based air conditioning units. The...). (a) Emission totals. Calculate an annual rate of refrigerant leakage from an air conditioning system... described in paragraph (b) of this section. Grams/YRSP = Emission rate for service ports and...

  7. 40 CFR 86.166-12 - Method for calculating emissions due to air conditioning leakage.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... determine a refrigerant leakage rate in grams per year from vehicle-based air conditioning units. The...). (a) Emission totals. Calculate an annual rate of refrigerant leakage from an air conditioning system... described in paragraph (b) of this section. Grams/YRSP = Emission rate for service ports and...

  8. Cover Crop Effects on Nitrous Oxide Emission from a Manure-Treated Mollisol

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Agriculture contributes 40% to 60% of the total annual N2O emissions to the atmosphere. Development of management practices to reduce these emissions would have a significant impact on greenhouse gas levels. Non-leguminous cover crops are efficient scavengers of residual soil NO3, thereby reducing l...

  9. Mercury emission from crematories in Japan

    NASA Astrophysics Data System (ADS)

    Takaoka, M.; Oshita, K.; Takeda, N.; Morisawa, S.

    2009-12-01

    Anthropogenic sources of mercury emissions have a significant impact on global pollution. Therefore, finding uncharacterised sources and assessing the emissions from these sources are important. However, limited data are available worldwide on mercury emissions from crematories. In Japan, 99.9% of dead bodies are cremated, which is the highest percentage in the world, and more than 1600 crematories are in operation. We thus focused on emissions from crematories in Japan. The number of targeted facilities was seven, and we used continuous emission monitoring to measure the mercury concentrations and investigate mercury behaviour. The total mercury concentrations in stack gases were a few μg/Nm3 (normal cubic meters). Considering the time profile of mercury and its species in cremations, the findings confirmed that the mercury in stack gas originated from dental amalgam. The amount of mercury emissions was calculated using the total concentration and gas flow rate. Furthermore, the annual amount of mercury emission from crematories in Japan was estimated by using the total number of corpses. The emission amount was considerably lower than that estimated in the UK. From statistical analyses on population demographics and measurements, future total emissions from crematories were also predicted. As a result, the amount of mercury emitted by crematories will likely increase by 2.6-fold from 2007 to 2037.

  10. Mercury emission from crematories in Japan

    NASA Astrophysics Data System (ADS)

    Takaoka, M.; Oshita, K.; Takeda, N.; Morisawa, S.

    2010-04-01

    Anthropogenic sources of mercury emissions have a significant impact on global pollution. Therefore, finding uncharacterised sources and assessing the emissions from these sources are important. However, limited data are available worldwide on mercury emissions from crematories. In Japan, 99.9% of dead bodies are cremated, which is the highest percentage in the world, and more than 1600 crematories are in operation. We thus focused on emissions from crematories in Japan. The number of targeted facilities was seven, and we used continuous emission monitoring to measure the mercury concentrations and investigate mercury behaviour. The total mercury concentrations in stack gases were a few μg/Nm3 (normal cubic meters). Considering the time profile of mercury and its species in cremations, the findings confirmed that the mercury in stack gas originated from dental amalgam. The amount of mercury emissions was calculated using the total concentration and gas flow rate. Furthermore, the annual amount of mercury emission from crematories in Japan was estimated by using the total number of corpses. The emission amount was considerably lower than that estimated in the United Kingdom. From statistical analyses on population demographics and measurements, future total emissions from crematories were also predicted. As a result, the amount of mercury emitted by crematories will likely increase by 2.6-fold from 2007 to 2037.

  11. N2O emissions from a nitrogen-enriched river

    USGS Publications Warehouse

    McMahon, P.B.; Dennehy, K.F.

    1999-01-01

    Nitrous oxide (N2O) emissions from the South Platte River in Colorado were measured using closed chambers in the fall, winter, and summer of 1994- 1995. The South Platte River was enriched in inorganic N (9-800 ??M) derived from municipal wastewater effluent and groundwater return flows from irrigated agricultural fields. River water was as much as 2500% supersaturated with N2O, and median N2O emission rates from the river surface ranged from less than 90 to 32 600 ??g-N m-2 d-1. Seventy-nine percent of the variance in N2O emission rates was explained by concentrations of total inorganic N in river water and by water temperature. The estimated total annual N2O emissions from the South Platte River were 2 x 1013-6 x 1013 ??g-N yr-1. This amount of annual N2O emissions was similar to the estimated annual N2O emissions from all primary municipal wastewater treatment processes in the United States (1). Results from this study indicate that N-enriched rivers could be important anthropogenic sources of N2O to the atmosphere. However, N2O emission measurements from other N-enriched rivers are needed to better quantify this source.Nitrous oxide (N2O) emissions from the South Platte River in Colorado were measured using closed chambers in the fall, winter, and summer of 1994-1995. The South Platte River was enriched in inorganic N (9-800 ??M) derived from municipal wastewater effluent and groundwater return flows from irrigated agricultural fields. River water was as much as 2500% supersaturated with N2O, and median N2O emission rates from the river surface ranged from less than 90 to 32 600 ??g-N m-2 d-1. Seventy-nine percent of the variance in N2O emission rates was explained by concentrations of total inorganic N in river water and by water temperature. The estimated total annual N2O emissions from the South Platte River were 2??1013-6??1013 ??g-N yr-1. This amount of annual N2O emissions was similar to the estimated annual N2O emissions from all primary municipal wastewater treatment processes in the United States. Results from this study indicate that N-enriched rivers could be important anthropogenic sources of N2O to the atmosphere. However, N2O emission measurements from other N-enriched rivers are needed to better quantify this source.

  12. Annual Energy Review, 2008

    SciTech Connect

    2009-06-01

    The Annual Energy Review (AER) is the Energy Information Administration's (EIA) primary report of annual historical energy statistics. For many series, data begin with the year 1949. Included are statistics on total energy production, consumption, trade, and energy prices; overviews of petroleum, natural gas, coal, electricity, nuclear energy, renewable energy, and international energy; financial and environment indicators; and data unit conversions.

  13. The role of [18F]fluoride positron emission tomography in the early detection of aseptic loosening of total knee arthroplasty.

    PubMed

    Sterner, T; Pink, R; Freudenberg, L; Jentzen, T; Quitmann, H; Bockisch, A; Löer, F

    2007-04-01

    Total knee arthroplasty is successful in the treatment of degenerative, arthritic or injured joints. But the most important long term complication seems to be aseptic loosening. An inflammatory process at the bone/cement or bone/prosthesis interface leads to a severe osteolysis. Although early diagnosis is very important the standard techniques often fail. [(18)F]Fluoride ion positron emission tomography (F-PET) is an appropriate tracer paired with a modern method for the evaluation of increased bone metabolism at the bone/prosthesis interface. In this preliminary study we describe for the first time the value of F-PET in the early diagnosis of aseptic loosening. We studied 14 painful knee arthoplasties. In 6 cases the definite diagnosis was determined by surgical procedure, for 8 cases a long clinical follow-up of the least 6 months after the onset of symptoms led to the diagnosis. The F-PET scans were obtained by with an ECAT EXACT HR+ scanner with and without attenuation correction in the two-and three-dimensional mode. An intermediate or high uptake along the bone/prosthesis or bone/cement interface including either the tibial stem or the half of the femoral component was suspected to be aseptic loose. The result were compared with plain radiographs. We found a sensitivity of 100%, a specificity of 56% and an accuracy of 71%. No false negative results were detected, in 4 patients one component as false positive. The sensitivity, specificity and accuracy for the plain radiograph of the same patients were 43%, 86% and 64%, respectively. In conclusion PET seems to be a promising new method in the early diagnosis of painful TKA because of its excellent spatial solution. In combination with the bone seeking tracer [(18) F]fluoride, PET allows the detection of aseptic loosening and the differentiation to the simple synovitis. Our preliminary results suggest that F-PET could be a useful tool although we examined a small group of patients. PMID:17448973

  14. The Seasonal and Spatial Distribution of Carbon Dioxide Emissions from Fossil Fuels in Asia

    NASA Astrophysics Data System (ADS)

    Gregg, J. S.; Andres, R. J.

    2006-12-01

    Carbon dioxide emissions from fossil-fuel consumption are presented for the five Asian countries that are among the global leaders in anthropogenic carbon emissions: China (13% of global total), Japan (5% of global total), India (5% of global total), South Korea (2% of global total), and Indonesia (1% of global total). Together, these five countries represent over a quarter of the world's fossil-fuel based carbon emissions. Moreover, these countries are rapidly developing and energy demand has grown dramatically in the last two decades. A method is developed to estimate the spatial and seasonal flux of fossil-fuel consumption, thereby greatly improving the temporal and spatial resolution of anthropogenic carbon dioxide emissions. Currently, only national annual data for anthropogenic carbon emissions are available, and as such, no understanding of seasonal or sub-national patterns of emissions are possible. This methodology employs fuel distribution data from representative sectors of the fossil-fuel market to determine the temporal and spatial patterns of fuel consumption. These patterns of fuel consumption are then converted to patterns of carbon emissions. The annual total emissions estimates produced by this method are consistent to those maintained by the United Nations. Improved estimates of temporal and spatial resolution of the human based carbon emissions allows for better projections about future energy demands, carbon emissions, and ultimately the global carbon cycle.

  15. 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.

  16. 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.

  17. 40 CFR 98.183 - Calculating GHG emissions.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... smelting furnace, determine the annual mass of carbon in each carbon-containing material, other than fuel... emissions using Equation R-1 of this section. Carbon-containing materials include carbonaceous reducing agents. If you document that a specific material contributes less than 1 percent of the total carbon...

  18. 40 CFR 98.183 - Calculating GHG emissions.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... smelting furnace, determine the annual mass of carbon in each carbon-containing material, other than fuel... emissions using Equation R-1 of this section. Carbon-containing materials include carbonaceous reducing agents. If you document that a specific material contributes less than 1 percent of the total carbon...

  19. 40 CFR 98.183 - Calculating GHG emissions.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... smelting furnace, determine the annual mass of carbon in each carbon-containing material, other than fuel... emissions using Equation R-1 of this section. Carbon-containing materials include carbonaceous reducing agents. If you document that a specific material contributes less than 1 percent of the total carbon...

  20. 40 CFR 98.183 - Calculating GHG emissions.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... smelting furnace, determine the annual mass of carbon in each carbon-containing material, other than fuel... emissions using Equation R-1 of this section. Carbon-containing materials include carbonaceous reducing agents. If you document that a specific material contributes less than 1 percent of the total carbon...

  1. 40 CFR 98.183 - Calculating GHG emissions.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... smelting furnace, determine the annual mass of carbon in each carbon-containing material, other than fuel... emissions using Equation R-1 of this section. Carbon-containing materials include carbonaceous reducing agents. If you document that a specific material contributes less than 1 percent of the total carbon...

  2. Effects of liquid aluminum chloride additions to poultry litter on broiler performance, ammonia emissions, soluble phosphorus, total volatile fatty acids, and nitrogen contents of litter

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Recent studies have shown that the use of aluminum sulfate (Al2(SO4)3.14H2O) and aluminum chloride (AlCl3) additions to animal manures are more effective than other chemicals in reducing ammonia (NH3) emissions and phosphorus (P) solubility. Although the use of alum has been intensively used in the ...

  3. Measurement of Total Site Mercury Emissions from Chlor-Alkali Plant Using Ultraviolet Differential Optical Absorption Spectroscopy and Cell Room Roof-Vent Monitoring

    EPA Science Inventory

    This technical note describes a United States Environmental Protection Agency (U.S. EPA) measurement project to determine elemental mercury (Hg0) emissions from a mercury cell chlor-alkali (MCCA) facility in the southeastern U.S. during a 53-day monitoring campaign in the fall of...

  4. A study to estimate and compare the total particulate matter emission indices (EIN) between traditional jet fuel and two blends of Jet A/Camelina biofuel used in a high by-pass turbofan engine: A case study of Honeywell TFE-109 engine

    NASA Astrophysics Data System (ADS)

    Shila, Jacob Joshua Howard

    The aviation industry is expected to grow at an annual rate of 5% until the year 2031 according to Boeing Outlook Report of 2012. Although the aerospace manufacturers have introduced new aircraft and engines technologies to reduce the emissions generated by aircraft engines, about 15% of all aircraft in 2032 will be using the older technologies. Therefore, agencies such as the National Aeronautics and Astronautics Administration (NASA), Federal Aviation Administration (FAA), the Environmental Protection Agency (EPA) among others together with some academic institutions have been working to characterize both physical and chemical characteristics of the aircraft particulate matter emissions to further understand their effects to the environment. The International Civil Aviation Organization (ICAO) is also working to establish an inventory with Particulate Matter emissions for all the aircraft turbine engines for certification purposes. This steps comes as a result of smoke measurements not being sufficient to provide detailed information on the effects of Particulate Matter (PM) emissions as far as the health and environmental concerns. The use of alternative fuels is essential to reduce the impacts of emissions released by Jet engines since alternative aviation fuels have been studied to lower particulate matter emissions in some types of engines families. The purpose of this study was to determine whether the emission indices of the biofuel blended fuels were lower than the emission indices of the traditional jet fuel at selected engine thrust settings. The biofuel blends observed were 75% Jet A-25% Camelina blend biofuel, and 50% Jet A-50% Jet A blend biofuel. The traditional jet fuel in this study was the Jet A fuel. The results of this study may be useful in establishing a baseline for aircraft engines' PM inventory. Currently the International Civil Aviation Organization (ICAO) engines emissions database contains only gaseous emissions data for only the TFE 731 and JT15D engines' families as representatives of other engines with rated thrust of 6000 pounds or below. The results of this study may be used to add to the knowledge of PM emission data that has been collected in other research studies. This study was quantitative in nature. Three factors were designated which were the types of fuels studied. The TFE-109 turbofan engine was the experimental subject. The independent variable was the engine thrust setting while the response variable was the emission index. Four engine runs were conducted for each fuel. In each engine run, four engine thrust settings were observed. The four engine thrust levels were 10%, 30%, 85%, and 100% rated thrusts levels. Therefore, for each engine thrust settings, there four replicates. The experiments were conducted using a TFE-109 engine test cell located in the Niswonger Aviation Technology building at the Purdue University Airport. The testing facility has the capability to conduct the aircraft PM emissions tests. Due to the equipment limitations, the study was limited to observe total PM emissions instead of specifically measuring the non-volatile PM emissions. The results indicate that the emissions indices of the blended biofuels were not statistically significantly lower compared to the emissions of the traditional jet fuel at rated thrust levels of 100% and 85% of TFE-109 turbofan engine. However, the emission indices for the 50%Jet A - 50%Camelina biofuel blend were statistically significantly lower compared to the emission indices of the 100% Jet A fuel at 10% and 30% engine rated thrusts levels of TFE-109 engine. The emission indices of the 50%-50% biofuel blend were lower by reductions of 15% and 17% at engine rated thrusts of 10% and 30% respectively compared to the emissions indices of the traditional jet fuel at the same engine thrust levels. Experimental modifications in future studies may provide estimates of the emissions indices range for this particular engine these estimates may be used to estimate the levels of PM emissions for other similar engines. Additional measurements steps such as heating of the sampling line, sampling dilution application, sampling line loss estimates, and calculations of the sampling line PM residence times will also be useful future results.

  5. Trends in anthropogenic mercury emissions in China from 1995 to 2003

    SciTech Connect

    Ye Wu; Shuxiao Wang; David G. Streets; Jiming Hao; Melissa Chan; Jingkun Jiang

    2006-09-01

    We have developed multiple-year inventories of anthropogenic mercury emissions in China for 1995 through 2003. It is estimated that total Hg emissions from all anthropogenic sources increased at an average annual rate of 2.9% during the period 1995-2003, reaching 696 ({+-}307) t in 2003, with a speciation split of 395 t of Hg{sup 0}, 230 t of Hg{sup 2+}, and 70 t of particulate mercury, Hg{sup p}. Nonferrous metals smelting and coal combustion continue to be the two leading mercury sources in China, as nonferrous metals production and coal consumption keep increasing. Nonferrous metals smelting and coal combustion together contributed {approximately}80% of total Hg emissions during the past decade. Hg emissions from coal combustion increased from 202 t in 1995 to 257 t in 2003 at an average annual rate of 3.0%. Among all of the coal consumption sectors, the power sector is the leading one in Hg emissions growth, up by 5.9% annually. Hg emissions from nonferrous metals smelting increased from 230 t in 1995 to 321 t in 2003 at an average annual rate of 4.2%. Although Hg emissions related to gold smelting decreased since 1996, other nonferrous metals such as zinc, lead, and copper contributed significant Hg growth at annual rates of 8.5%, 13.0%, and 6.9%, respectively. At provincial level, the trends of Hg emissions show significant variation. The uncertainty level decreased from {+-}78% (95% confidence interval) in the estimate of total emissions in 1995, to {+-}44% in 2003. This is primarily attributed to the decreased emissions from those Hg sources with the largest uncertainty in both activity levels and emission factors, such as artisanal gold smelting, mercury mining, and battery/fluorescent lamp production. 36 refs., 2 figs., 4 tabs.

  6. Mercury emissions from biomass burning in China.

    PubMed

    Huang, Xin; Li, Mengmeng; Friedli, Hans R; Song, Yu; Chang, Di; Zhu, Lei

    2011-11-01

    Biomass burning covers open fires (forest and grassland fires, crop residue burning in fields, etc.) and biofuel combustion (crop residues and wood, etc., used as fuel). As a large agricultural country, China may produce large quantities of mercury emissions from biomass burning. A new mercury emission inventory in China is needed because previous studies reflected outdated biomass burning with coarse resolution. Moreover, these studies often adopted the emission factors (mass of emitted species per mass of biomass burned) measured in North America. In this study, the mercury emissions from biomass burning in China (excluding small islands in the South China Sea) were estimated, using recently measured mercury concentrations in various biomes in China as emission factors. Emissions from crop residues and fuelwood were estimated based on annual reports distributed by provincial government. Emissions from forest and grassland fires were calculated by combining moderate resolution imaging spectroradiometer (MODIS) burned area product with combustion efficiency (ratio of fuel consumption to total available fuels) considering fuel moisture. The average annual emission from biomass burning was 27 (range from 15.1 to 39.9) Mg/year. This inventory has high spatial resolution (1 km) and covers a long period (2000-2007), making it useful for air quality modeling. PMID:21950526

  7. The importance of policy in emissions inventory accuracy--a lesson from British Columbia, Canada.

    PubMed

    Krzyzanowski, Judi

    2009-04-01

    Actual atmospheric emissions in northeast British Columbia, Canada, are much higher than reported emissions. The addition of upstream oil and gas sector sources not included in the year-2000 emissions inventory of Criteria Air Contaminants (CACs) increases annual totals of nitrogen oxides, sulfur oxides, and volatile organic compound emissions by 115.1, 89.9, and 109.5%, respectively. These emissions arise from numerous small and unregulated point sources (N = 10,129). CAC summaries are given by source type and source sector. An analysis of uncertainty and reporting policy suggests that inventory omissions are not limited to the study area and that Canadian pollutant emissions are systematically underestimated. The omissions suggest that major changes in reporting procedures are needed in Canada if true estimates of annual pollutant emissions are to be documented. PMID:19418817

  8. 40 CFR 63.5870 - How do I calculate annual uncontrolled and controlled organic HAP emissions from my wet-out area...

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... lamination/casting operations? 63.5870 Section 63.5870 Protection of Environment ENVIRONMENTAL PROTECTION... lamination/casting operations? To calculate your annual uncontrolled and controlled organic HAP...

  9. Assessing global radiative forcing due to regional emissions of tropospheric ozone precursors: a step towards climate credit for ozone reductions

    NASA Astrophysics Data System (ADS)

    Mauzerall, D. L.; Naik, V.; Horowitz, L. W.; Schwarzkopf, D.; Ramaswamy, V.; Oppenheimer, M.

    2005-05-01

    Carbon dioxide emissions from fossil-fuel consumption are presented for the five Asian countries that are among the global leaders in anthropogenic carbon emissions: China (13% of global total), Japan (5% of global total), India (5% of global total), South Korea (2% of global total), and Indonesia (1% of global total). Together, these five countries represent over a quarter of the world's fossil-fuel based carbon emissions. Moreover, these countries are rapidly developing and energy demand has grown dramatically in the last two decades. A method is developed to estimate the spatial and seasonal flux of fossil-fuel consumption, thereby greatly improving the temporal and spatial resolution of anthropogenic carbon dioxide emissions. Currently, only national annual data for anthropogenic carbon emissions are available, and as such, no understanding of seasonal or sub-national patterns of emissions are possible. This methodology employs fuel distribution data from representative sectors of the fossil-fuel market to determine the temporal and spatial patterns of fuel consumption. These patterns of fuel consumption are then converted to patterns of carbon emissions. The annual total emissions estimates produced by this method are consistent to those maintained by the United Nations. Improved estimates of temporal and spatial resolution of the human based carbon emissions allows for better projections about future energy demands, carbon emissions, and ultimately the global carbon cycle.

  10. Estimating CH4 Emissions in California Using Measurements from a Tower Network

    NASA Astrophysics Data System (ADS)

    Jeong, S.; Hsu, Y.; Andrews, A. E.; Bianco, L.; Vaca, P.; Wilczak, J. M.; Fischer, M. L.

    2012-12-01

    We estimate regionally resolved methane (CH4) emissions for California using a Bayesian inverse model driven by CH4 mixing ratios measured at a network of five towers across the Central Valley during 2010 - 2011. The method estimates emissions by comparing measurements with transport model predictions of CH4 signals obtained from two 0.1 degree prior emission maps: 1) seasonally varying "California-specific" emission maps, calibrated to State emission totals, and 2) the EDGAR4.2 static global emission map. Atmospheric transport is calculated from particle trajectories and surface footprints using the Weather Research and Forecasting (WRF) and Stochastic Time-Inverted Lagrangian Transport (STILT) models. Results for the 5-tower CARB-CEC-LBNL-NOAA network show that significant reductions in posterior emissions uncertainty are obtained for regions comprising ~ 90% of California's known CH4 emissions, with annually averaged emissions totaling 1.6+/-0.1 and 2.5+/-0.3 times California's inventory for the California-specific and EDGAR4.2 emissions maps, respectively. Assuming these results apply across California, total CH4 emissions account for approximately 8% - 14% of current state total greenhouse gas emissions. The magnitude and uncertainty of emissions from specific regions and source sectors (e.g., crop agriculture, waste management, livestock, and energy activities) are estimated by comparing region and source sector results obtained with the CA-specific and EDGAR4.2 emission maps.

  11. Total protein

    MedlinePlus

    The total protein test measures the total amount of two classes of proteins found in the fluid portion of your blood. These are albumin and globulin. Proteins are important parts of all cells and tissues. ...

  12. 77 FR 64463 - Annual Retail Trade Survey

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-10-22

    ..., the Census Bureau will collect data covering annual sales, annual e- commerce sales, year-end..., accounts receivables, and, for selected industries, merchandise line sales, and percent of e-commerce sales..., annual sales, annual e-commerce sales, purchases, total and detailed operating expenses,...

  13. 75 FR 63804 - Annual Retail Trade Survey

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-10-18

    ... survey, the Census Bureau will collect data covering annual sales, annual e-commerce sales, year-end... percent of e-commerce sales to customers located outside the United States. These data are collected to... classification basis, annual sales, annual e-commerce sales, purchases, total operating expenses,...

  14. Methane emissions to the troposphere from the Amazon floodplain

    NASA Technical Reports Server (NTRS)

    Devol, Allen H.; Richey, Jeffrey E.; Clark, Wayne A.; King, Stagg L.; Martinelli, Luiz A.

    1988-01-01

    The magnitudes of CH4 emissions to the troposphere from the Amazon River floodplain and the mechanism of these emissions were investigated using the data of 94 individual flux measurements made along a 1700-km stretch of the river during July/August 1985. The overall average rate of CH4 emission from wetlands was found to be 390 mg CH4/sq m per day, with the highest emissions (590 mg CH4/sq m per day) attributed to the water surfaces covered by aquatic macrophytes. Ebullition was the dominant mechanism of emission, accounting for 85 percent of the total. Surface-water CH4 concentrations were highly supersaturated, averaging 6.4 micromolar. The annual emission of CH4 from the Amazon Basin to the troposphere, estimated from the area and the known emission rate, is about 10 CH4 Tg/yr, indicating the importance of the area in the global atmospheric CH4 cycle.

  15. Uncertainties of modelling emissions from road transport

    NASA Astrophysics Data System (ADS)

    Kühlwein, J.; Friedrich, R.

    To determine emission data from road transport, complex methods and models are applied. Emission data are characterized by a huge variety of source types as well as a high resolution of the spatial allocation and temporal variation. So far, the uncertainties of such calculated emission data have been largely unknown. As emission data is used to aid policy decisions, the accuracy of the data should be known. So, in the following, the determination of uncertainties of emission data is described. Using the IER emission model for generating regional or national emission data, the uncertainties of model input data and the total errors on different aggregation levels are exemplarily investigated for the pollutants NO x and NMHC in 1994 for the area of West Germany. The results of statistical error analysis carried out for annual emissions on road sections show variation coefficients (68.3% confidence interval) of 15-25%. In addition, systematic errors of common input data sets have been identified especially affecting emissions on motorway sections. The statistical errors of urban emissions with warm engine on town level amount to 35%. Therefore they are considerably higher than the errors outside towns. Error ranges of additional cold start emissions determined so far have been found in the same order. Additional uncertainties of temporally highly resolved (hourly) emission data depend strongly on the daytime, the weekday and the road category. Variation coefficients have been determined in the range between 10 and 70% for light-duty vehicles and between 15 and 100% for heavy-duty vehicles. All total errors determined here have to be regarded as lower limits of the real total errors.

  16. Application of particle size distributions to total particulate stack samples to estimate PM2.5 and PM10 emission factors for agricultural sources

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Particle size distributions (PSD) have long been used to more accurately estimate the PM10 fraction of total particulate matter (PM) stack samples taken from agricultural sources. These PSD analyses were typically conducted using a Coulter Counter with 50 micrometer aperture tube. With recent increa...

  17. A comparison on the emission of polycyclic aromatic hydrocarbons and their corresponding carcinogenic potencies from a vehicle engine using leaded and lead-free gasoline.

    PubMed Central

    Mi, H H; Lee, W J; Tsai, P J; Chen, C B

    2001-01-01

    Our objective in this study was to assess the effect of using two kinds of lead-free gasoline [including 92-lead-free gasoline (92-LFG) and 95-lead-free gasoline (95-LFG), rated according to their octane levels] to replace the use of premium leaded gasoline (PLG) on the emissions of polycyclic aromatic hydrocarbons (PAHs) and their corresponding benzo[a]pyrene equivalent (BaP(eq)) amounts from the gasoline-powered engine. The results show that the three gasoline fuels originally contained similar total PAHs and total BaP(eq) contents; however, we found significant differences in the engine exhausts in both contents. The above results suggest that PAHs originally contained in the gasoline fuel did not affect the PAH emissions in the engine exhausts. The emission factors of both total PAHs and total BaP(eq) obtained from the three gasoline fuels shared the same trend: 95-LFG > PLG > 92-LFG. The above result suggests that when PLG was replaced by 95-LFG, the emissions would increase in both total PAHs and total BaP(eq), but when replaced by 92-LFG would lead to the decreased emissions of both contents. By taking emission factors and their corresponding annual gasoline consumption rates into account, we found that both total PAH and total BaP(eq) emissions increased from 1994 to 1999. However, the annual increasing rates in total BaP(eq) emissions were slightly higher than the corresponding increasing rates in total PAHs. PMID:11748037

  18. Impact of Changes in Barometric Pressure on Landfill Methane Emission

    NASA Astrophysics Data System (ADS)

    McDermitt, Dayle; Xu, Liukang; Lin, Xiaomao; Amen, Jim; Welding, Karla

    2013-04-01

    Landfill methane emissions were measured continuously using the eddy covariance method from June to December 2010. The study site was located at the Bluff Road Landfill in Lincoln, Nebraska USA. Methane emissions strongly depended on changes in barometric pressure; rising barometric pressure suppressed the emission, while falling barometric pressure enhanced the emission. Emission rates were systematically higher in December than during the summer period. Higher methane emission rates were associated with changes in barometric pressure that were larger in magnitude and longer in duration in winter than in summer, and with lower mean temperatures, which appeared to reduce methane oxidation rates. Sharp changes in barometric pressure caused up to 35-fold variation in day-to-day methane emissions. Power spectrum and ogive analysis showed that continuous measurements over a period of at least 10 days were needed in order to capture 90% of total variance in the methane emission time series at our site. Our results suggest that point-in-time methane emission rate measurements taken at monthly or even longer time intervals using techniques such as the tracer plume method, the mass balance method, or the closed-chamber method may be subject to large variations because of the strong dependence of methane emissions on changes in barometric pressure. Estimates of long-term integrated methane emissions from landfills based on such measurements will inevitably yield large uncertainties. Our results demonstrate the value of continuous measurements for quantifying total annual methane emission from a landfill.

  19. Seasonal variations in N2O emissions from central California

    NASA Astrophysics Data System (ADS)

    Jeong, Seongeun; Zhao, Chuanfeng; Andrews, Arlyn E.; Dlugokencky, Edward J.; Sweeney, Colm; Bianco, Laura; Wilczak, James M.; Fischer, Marc L.

    2012-08-01

    We estimate nitrous oxide (N2O) emissions from Central California for the period of December 2007 through November 2009 by comparing N2O mixing ratios measured at a tall tower (Walnut Grove, WGC) with transport model predictions based on two global a priori N2O emission models (EDGAR32 and EDGAR42). Atmospheric particle trajectories and surface footprints are computed using the Weather Research and Forecasting (WRF) and Stochastic Time-Inverted Lagrangian Transport (STILT) models. Regression analyses show that the slopes of predicted on measured N2O from both emission models are low, suggesting that actual N2O emissions are significantly higher than the EDGAR inventories for all seasons. Bayesian inverse analyses of regional N2O emissions show that posterior annual N2O emissions are larger than both EDGAR inventories by factors of 2.0 ± 0.4 (EDGAR32) and 2.1 ± 0.4 (EDGAR42) with seasonal variation ranging from 1.6 ± 0.3 to 2.5 ± 0.4 for an influence region of Central California within approximately 150 km of the tower. These results suggest that if the spatial distribution of N2O emissions in California follows the EDGAR emission models, then actual emissions are 2.7 ± 0.5 times greater than the current California emission inventory, and total N2O emissions account for 8.1 ± 1.4% of total greenhouse gas emissions from California.

  20. Contribution of Solar Hydrogen Lyα Line Emission in Total Ionization Rate in Ionospheric D-region During the Maximum of Solar X-flare

    NASA Astrophysics Data System (ADS)

    Nina, A.; Čadež, V. M.; Bajčetić, J.

    2015-12-01

    The solar Lyα line emission can be considered as the dominant source of ionization processes in the ionospheric D-region at altitudes above 70 km during unperturbed conditions. However, large sudden impacts of radiation in some other energy domains can also significantly influence the ionization rate and, in this paper, we present a study on the contribution of Lyα radiation to the ionization rate when the ionosphere is disturbed by solar X-flares. We give relevant analytical expressions and make calculations and numerical simulations for the low ionosphere using data collected by the VLF receiver located in Serbia for the VLF radio signal emitted by the DHO transmitter in Germany.

  1. Effect of progressive inoculation of fauna-free sheep with holotrich protozoa and total-fauna on rumen fermentation, microbial diversity and methane emissions

    PubMed Central

    Belanche, Alejandro; de la Fuente, Gabriel; Newbold, Charles J.

    2014-01-01

    Rumen methanogenesis represents an energy waste for the ruminant and an important source of greenhouse gas; thus, integrated studies are needed to fully understand this process. Eight fauna-free sheep were used to investigate the effect of successive inoculation with holotrich protozoa then with total fauna on rumen methanogenesis. Holotrichs inoculation neither altered rumen fermentation rate nor diet digestibility, but increased concentrations of acetate (+15%), butyrate (+57%), anaerobic fungi (+0.82 log), methanogens (+0.41 log) and methanogenesis (+54%). Further inoculation with total fauna increased rumen concentrations of protozoa (+1.0 log), bacteria (+0.29 log), anaerobic fungi (+0.78 log), VFA (+8%), ammonia and fibre digestibility (+17%) without affecting levels of methanogens or methanogenesis. Rumen methanogens population was fairly stable in terms of structure and diversity, while the bacterial community was highly affected by the treatments. Inoculation with holotrich protozoa increased bacterial diversity. Further inoculation with total fauna lowered bacterial diversity but increased concentrations of certain propionate and lactate-producing bacteria, suggesting that alternative H2 sinks could be relevant. This experiment suggests that holotrich protozoa have a greater impact on rumen methanogenesis than entodiniomorphids. Thus, further research is warranted to understand the effect of holotrich protozoa on methane formation and evaluate their elimination from the rumen as a potential methane mitigation strategy. PMID:25764558

  2. Effect of progressive inoculation of fauna-free sheep with holotrich protozoa and total-fauna on rumen fermentation, microbial diversity and methane emissions.

    PubMed

    Belanche, Alejandro; de la Fuente, Gabriel; Newbold, Charles J

    2015-03-01

    Rumen methanogenesis represents an energy waste for the ruminant and an important source of greenhouse gas; thus, integrated studies are needed to fully understand this process. Eight fauna-free sheep were used to investigate the effect of successive inoculation with holotrich protozoa then with total fauna on rumen methanogenesis. Holotrichs inoculation neither altered rumen fermentation rate nor diet digestibility, but increased concentrations of acetate (+15%), butyrate (+57%), anaerobic fungi (+0.82 log), methanogens (+0.41 log) and methanogenesis (+54%). Further inoculation with total fauna increased rumen concentrations of protozoa (+1.0 log), bacteria (+0.29 log), anaerobic fungi (+0.78 log), VFA (+8%), ammonia and fibre digestibility (+17%) without affecting levels of methanogens or methanogenesis. Rumen methanogens population was fairly stable in terms of structure and diversity, while the bacterial community was highly affected by the treatments. Inoculation with holotrich protozoa increased bacterial diversity. Further inoculation with total fauna lowered bacterial diversity but increased concentrations of certain propionate and lactate-producing bacteria, suggesting that alternative H2 sinks could be relevant. This experiment suggests that holotrich protozoa have a greater impact on rumen methanogenesis than entodiniomorphids. Thus, further research is warranted to understand the effect of holotrich protozoa on methane formation and evaluate their elimination from the rumen as a potential methane mitigation strategy. PMID:25764558

  3. 2008 annual merit review

    SciTech Connect

    None, None

    2009-01-18

    The 2008 DOE Vehicle Technologies Program Annual Merit Review was held February 25-28, 2008 in Bethesda, Maryland. The review encompassed all of the work done by the Vehicle Technologies Program: a total of 280 individual activities were reviewed, by a total of just over 100 reviewers. A total of 1,908 individual review responses were received for the technical reviews, and an additional 29 individual review responses were received for the plenary session review.

  4. Methane and nitrous oxide (N{sub 2}O) emission characteristics from automobiles

    SciTech Connect

    Koike, Noriyuki; Odaka, Matsuo

    1996-09-01

    Exhaust gases discharged from automobiles are noticed as one of the reasons for recent increase in atmospheric methane and nitrous oxide concentration, which have been considered as greenhouse gases. In order to make an accurate estimation of methane and nitrous oxide discharged from automobiles, measurement methods were experimentally developed and emissions were measured for different kinds of automobiles under various driving conditions. Then, the authors have tried to estimate the annual global emissions from automobiles using these measurement results and statistical data such as the number of automobiles, the total annual mileage, and the total annual fuel consumption, etc. The emissions from passenger vehicles which have been estimated from the global number of automobiles were 477.263 t/year for methane and 313.472 t/year for nitrous oxide. These numbers are higher than what had been estimated.

  5. Polychlorinated dibenzo-p-dioxin and dibenzofuran emissions from an industrial park clustered with metallurgical industries.

    PubMed

    Wang, Jenshi B; Hung, Chung-Hsien; Hung, Chung-Hsuang; Chang-Chien, Guo-Ping

    2009-01-30

    Emissions of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) from an industrial park operated as Taiwan's center of metallurgical industries were investigated. The characteristics of mean PCDD/F I-TEQ concentrations, congener profiles and emission factors of each source were studied over samples of stack flue gases of individual sources. Different characteristics of congener profiles and large variations of emission factors of secondary aluminum smelters (ALSs) were observed. The mean emission factors of electric arc furnaces were comparable to those for ALSs and much greater than those of municipal solid waste incinerators and sinter plants, but still less than that of clinical waste incinerators. Annual PCDD/F emission contribution of each source was estimated, raising critical concerns over the overall PCDD/F emissions from metallurgical processes. The metallurgical industries altogether contributed approximately 98.1% of the total annual emissions, while waste incinerators only 1.9%. The contributions by sinter plants and metallurgical industries to the total annual emissions of the Park were much higher than the corresponding national averages of Taiwan. The combined dioxin emissions from the entire metallurgical processes and their controls should be seriously envisaged by industrial parks devoted to metal productions. PMID:18538923

  6. Modeling of pesticide emissions from agricultural ecosystems

    NASA Astrophysics Data System (ADS)

    Li, Rong

    2012-04-01

    Pesticides are applied to crops and soils to improve agricultural yields, but the use of pesticides has become highly regulated because of concerns about their adverse effects on human health and environment. Estimating pesticide emission rates from soils and crops is a key component for risk assessment for pesticide registration, identification of pesticide sources to the contamination of sensitive ecosystems, and appreciation of transport and fate of pesticides in the environment. Pesticide emission rates involve processes occurring in the soil, in the atmosphere, and on vegetation surfaces and are highly dependent on soil texture, agricultural practices, and meteorology, which vary significantly with location and/or time. To take all these factors into account for simulating pesticide emissions from large agricultural ecosystems, this study coupled a comprehensive meteorological model with a dynamic pesticide emission model. The combined model calculates hourly emission rates from both emission sources: current applications and soil residues resulting from historical use. The coupled modeling system is used to compute a gridded (36 × 36 km) hourly toxaphene emission inventory for North America for the year 2000 using a published U.S. toxaphene residue inventory and a Mexican toxaphene residue inventory developed using its historical application rates and a cropland inventory. To my knowledge, this is the first such hourly toxaphene emission inventory for North America. Results show that modeled emission rates have strong diurnal and seasonal variations at a given location and over the entire domain. The simulated total toxaphene emission from contaminated agricultural soils in North America in 2000 was about 255 t, which compares reasonably well to a published annual estimate. Most emissions occur in spring and summer, with domain-wide emission rates in April, May and, June of 36, 51, and 35 t/month, respectively. The spatial distribution of emissions depends on the distribution of toxaphene soil residues, and high emission rates coincide with heavily contaminated areas.

  7. Development of criteria for extension of applicability of low emission, high efficiency coal burners: second annual report. Report for Oct 78-Sep 79

    SciTech Connect

    Brienza, A.; Chen, S.; Heap, M.; Lee, J.; Nurick, W.

    1984-02-01

    The report, describing the second year's effort under this contract, concerns the development of criteria for the evaluation and applicability of low-emission, high efficiency coal burners. The report describes progress in three major areas: (1) bench scale studies, (2) distributed mixing burner (DMB) development, and (3) comparison with commercial practice. No operability problems were encountered with different fuel types, but NO emissions were fuel dependent. Several commercial burners were tested satisfactorily in the test facility.

  8. International energy annual 1996

    SciTech Connect

    1998-02-01

    The International Energy Annual presents an overview of key international energy trends for production, consumption, imports, and exports of primary energy commodities in over 220 countries, dependencies, and areas of special sovereignty. Also included are population and gross domestic product data, as well as prices for crude oil and petroleum products in selected countries. Renewable energy reported in the International Energy Annual includes hydroelectric power, geothermal, solar, and wind electric power, biofuels energy for the US, and biofuels electric power for Brazil. New in the 1996 edition are estimates of carbon dioxide emissions from the consumption of petroleum and coal, and the consumption and flaring of natural gas. 72 tabs.

  9. Obtaining Electron Temperatures and Flow Speeds from Thomson Scattered Coronal Emission Observed during the 29 March 2006 Total Solar Eclipse in Libya

    NASA Technical Reports Server (NTRS)

    Davila, Joseph M.; Geginald, Nelson L.; Gashut, Hadi; Guhathakurta, Madhulika; Hassler, Donald M.

    2008-01-01

    An experiment to measure the electron temperature and flow speed in the solar corona by observing the visible K-coronal spectrum was conducted during the total solar eclipse on 29 March 2006 in Libya. New corona1 models accounting for the effect of electron temperature and flow on the resulting K-corona spectrum were used to interpret the observations. Results show electron temperatures of 1.10 +/- 0.05, 0.98 +/- 0.12, and 0.70 +/- 0.08 MK, at l.l{\\it R)$-{\\odot)$ in the solar north, east and west, respectively, and 0.93 +/- 0.12 MK, at 1.2 R(sub sun) in the solar east. The corresponding outflow speeds obtained from the spectral fit are 103 +/- 92, 0 + 10, 0 + 10, and 0 + 10 km/s. Since the observations are taken only at 1.1 and 1.2 R(sub sun) these velocities , consistent with zero outflow, are in agreement with expectations and provide additional confirmation that the spectral fitting method is working.

  10. β - γ and β-neutron- γ emission in mass A=137 Decay Chain Studied with the Modular Total Absorption Spectrometer (MTAS)

    NASA Astrophysics Data System (ADS)

    Rasco, Charles; Fijałkowska, Aleksandra; Karny, Marek; Rykaczewski, Krzysztof; Wolińska-Cichocka, Marzena; Grzywacz, Robert

    2013-10-01

    The Modular Total Absorption Spectrometer (MTAS) is a detector made up of 19 separate hexagon modules of NaI which results in over a ton of NaI in the MTAS detector. MTAS was designed to capture as much of the electromagnetic energy release in β-decays as possible. MTAS was constructed at the Holifield Radioactive Ion Beam Facility and measured over 20 decay products of 238U fission products in its inaugural measurement campaign in January 2012. The measurements were focused on nuclei identified as important for decay heat analysis of the nuclear fuel cycle. Silicon detectors placed at the center of MTAS to provide β triggers, make for extremely clean signals in MTAS. Preliminary results on the average electromagnetic energy release in the β decay of 137Xe and 137I isotopes will be presented. These isotopes are among the priority 1 cases listed by the NEA. The 137I also has a beta -neutron decay branch that is detected in MTAS. Neutron detection in a large NaI detector will also be discussed. This work was supported by the US DOE by award no. DE-FG02-96ER40978 and by US DOE, Office of Nuclear Physics.

  11. Evaluation of sample preparation methods for the detection of total metal content using inductively coupled plasma optical emission spectrometry (ICP-OES) in wastewater and sludge

    NASA Astrophysics Data System (ADS)

    Dimpe, K. M.; Ngila, J. C.; Mabuba, N.; Nomngongo, P. N.

    Heavy metal contamination exists in aqueous wastes and sludge of many industrial discharges and domestic wastewater, among other sources. Determination of metals in the wastewater and sludge requires sample pre-treatment prior to analysis because of certain challenges such as the complexity of the physical state of the sample, which may lead to wrong readings in the measurement. This is particularly the case with low analyte concentration to be detected by the instrument. The purpose of this work was to assess and validate the different sample preparation methods namely, hot plate and microwave-assisted digestion procedures for extraction of metal ions in wastewater and sludge samples prior to their inductively coupled plasma optical emission spectrometric (ICP-OES) determination. For the extraction of As, Al, Cd, Cr, Cu, Fe, Mn, Ni, Pb, Zn, three acid mixtures, that is, HNO3/H2O2, HNO3/HClO4/H2O2 and aqua regia + H2O2, were evaluated. Influent wastewater spiked with the SRM (CWW-TM-B) was used for the optimization of acid mixtures affecting the extraction procedure. After sample digestion, the filtration capabilities of cellulose-acetate filter paper and the acrodisc syringe filter with the pore size of 0.45 μm were compared. In terms of performance, acrodisc syringe filter in terms of the improved recoveries obtained, was found to be the best filtration method compared to the filter paper. Based on the analytical results obtained, microwave-assisted digestion (MAD) using aqua regia + H2O2 mixture was found to be the most suitable method for extraction of heavy metals and major elements in all the sample matrices. Therefore, MAD using aqua regia + H2O2 mixture was used for further investigations. The precision of the developed MAD method expressed in terms of relative standard deviations (% RSD) for different metals was found to be <5%. The limits of detection (LOD) and limits of quantification (LOQ) ranged from 0.12% to 2.18 μg L-1 and 0.61% to 3.43 μg L-1, respectively. The accuracy of the developed method (MAD using aqua regia + H2O2) was verified by analyzing two SRMs (CWW-TM-A and CWW-TM-B) and the obtained results were in agreement with certified values with recoveries ranging from 80% to 104% for CWW-TM-A and 84% to 102% for CWW-TM-B. The accuracy of the developed method was verified also by the recovery test in the spiked sludge samples. The accuracy and spike recovery test for different metal ions were in the range 80-104% and 92-106%, respectively. The developed method was applied for extraction of the As, Al, Cd, Cr, Cu, Fe, Mn, Ni, Pb, Zn in environmental samples, namely wastewater and sludge.

  12. Emissions from South Asian brick production.

    PubMed

    Weyant, Cheryl; Athalye, Vasudev; Ragavan, Santhosh; Rajarathnam, Uma; Lalchandani, Dheeraj; Maithel, Sameer; Baum, Ellen; Bond, Tami C

    2014-06-01

    Thirteen South Asian brick kilns were tested to quantify aerosol and gaseous pollutant emissions. Particulate matter (PM2.5), carbon monoxide (CO), and optical scattering and absorption measurements in the exhaust of six kiln technologies demonstrate differences in overall emission profiles and relative climate warming resulting from kiln design and fuel choice. Emission factors differed between kiln types, in some cases by an order of magnitude. The kilns currently dominating the sector had the highest emission factors of PM2.5 and light absorbing carbon, while improved Vertical Shaft and Tunnel kilns were lower emitters. An improved version of the most common technology in the region, the zig-zag kiln, was among the lowest emitting kilns in PM2.5, CO, and light absorbing carbon. Emission factors measured here are lower than those currently used in emission inventories as inputs to global climate models; 85% lower (PM2.5) and 35% lower for elemental carbon (EC) for the most common kiln in the region, yet the ratio of EC to total carbon was higher than previously estimated (0.96 compared to 0.47). Total annual estimated emissions from the brick industry are 120 Tg CO2, 2.5 Tg CO, 0.19 Tg PM2.5, and 0.12 Tg EC. PMID:24735080

  13. Oxygenated VOC and monoterpene emissions from a boreal coniferous forest

    NASA Astrophysics Data System (ADS)

    Taipale, R.; Rantala, P.; Kajos, M. K.; Patokoski, J.; Ruuskanen, T. M.; Aalto, J.; Kolari, P.; Bäck, J.; Hari, P.; Kulmala, M.; Rinne, J.

    2012-04-01

    Compared with terpenoids, emissions of oxygenated volatile organic compounds (VOCs) from boreal ecosystems have been poorly characterized. We measured ecosystem scale emissions of three oxygenated compounds (methanol, acetaldehyde, and acetone) and monoterpenes from a Scots pine dominated forest in southern Finland during the summers 2006-2008. The measurements were conducted using the disjunct eddy covariance method combined with proton transfer reaction mass spectrometry. The contribution of the three oxygenated compounds to the measured total emissions was 40-60 %. The highest oxygenated VOC emissions were those of methanol, comprising 20-30 % of the total, followed by acetone with a share of 10-20 %. The acetaldehyde emissions were 5-10 % of the total. This emission composition will be compared with that obtained from shoot enclosure measurements. Methanol showed deposition during some periods although its overall flux was towards the atmosphere. The monoterpene emissions had a light dependent component, suggesting that part of the emissions originated directly from monoterpene biosynthesis. Diurnal, seasonal, and inter-annual variations in the emissions, along with temperature and light dependencies, will be discussed.

  14. Inter-annual variability of wintertime PM2.5 chemical composition in Xi'an, China: Evidences of changing source emissions.

    PubMed

    Xu, Hongmei; Cao, Junji; Chow, Judith C; Huang, R-J; Shen, Zhenxing; Chen, L W Antony; Ho, Kin Fai; Watson, John G

    2016-03-01

    Chemical characteristics of PM2.5 in Xi'an in wintertime of 2006, 2008, and 2010 were investigated. Markers of OC2, EC1, and NO3(-)/SO4(2-) ratio were calculated to investigate the changes in PM2.5 emission sources over the 5-year period. Positive matrix factorization (PMF) model was used to identify and quantify the main sources of PM2.5 and their contributions. The results showed that coal combustion, motor vehicular emissions, fugitive dust, and secondary inorganic aerosol accounted for more than 80% of PM2.5 mass. The importance of these major sources to the PM2.5 mass varied yearly: coal combustion was the largest contributor (31.2% ± 5.2%), followed by secondary inorganic aerosol (20.9% ± 5.2%) and motor vehicular emissions (19.3% ± 4.8%) in 2006; the order was still coal combustion emissions (27.6% ± 3.4%), secondary inorganic aerosol (23.2% ± 6.9%), and motor vehicular emissions (20.9% ± 4.6%) in 2008; while coal combustion emission further decreased (24.1% ± 3.1%) with fugitive dust (19.4% ± 5.5%) increasing in 2010. The changes in PM2.5 chemical compositions and source contributions can be attributed to the social and economic developments in Xi'an, China, including energy structure adjustment, energy consumption, the expansion of civil vehicles, and the increase of urban construction activities. PMID:26760274

  15. Isoprene and monoterpene emissions from an Inner Mongolia grassland

    NASA Astrophysics Data System (ADS)

    Bai, Jianhui; Baker, Bradly; Liang, Baosheng; Greenberg, James; Guenther, Alex

    Terpenoid emissions were measured at a grassland site in Inner Mongolia, China during four campaigns over a 2-year period. Emissions were strongly correlated with light and temperature and the variations could be simulated using a canopy emission model. Substantial seasonal and interannual variations in isoprene emissions were also observed. Area averaged isoprene emissions normalized to standard above-canopy temperature and light conditions (30 °C and 1500 μmol m -2 s -1) ranged from about 50 to 500 μg m -2 h -1. These rates are more than an order of magnitude higher than those previously reported for temperate grasslands but are lower than emission rates observed from ground cover vegetation at higher latitudes. Isoprene emissions from this Inner Mongolia grassland may be dominated by emissions from sedges, e.g. Carex appendiculata. Total monoterpene emissions normalized to a standard temperature of 30 °C were only about 3 μg m -2 h -1 and consisted primarily of carene and limonene with smaller contributions of α-pinene and β-pinene. A model sensitivity study showed that grass and other herbaceous ground cover can contribute >10% of the total isoprene emission from certain regions, such as Inner Mongolia, but are<4% on a global annual scale.

  16. Historical evaluation of vehicle emission control in Guangzhou based on a multi-year emission inventory

    NASA Astrophysics Data System (ADS)

    Zhang, Shaojun; Wu, Ye; Liu, Huan; Wu, Xiaomeng; Zhou, Yu; Yao, Zhiliang; Fu, Lixin; He, Kebin; Hao, Jiming

    2013-09-01

    The Guangzhou government adopted many vehicle emission control policies and strategies during the five-year preparation (2005-2009) to host the 2010 Asian Games. This study established a multi-year emission inventory for vehicles in Guangzhou during 2005-2009 and estimated the uncertainty in total vehicle emissions by taking the assumed uncertainties in fleet-average emission factors and annual mileage into account. In 2009, the estimated total vehicle emissions in Guangzhou were 313 000 (242 000-387 000) tons of CO, 60 900 (54 000-70 200) tons of THC, 65 600 (56 800-74 100) tons of NOx and 2740 (2100-3400) tons of PM10. Vehicle emissions within the urban area of Guangzhou were estimated to be responsible for ˜40% of total gaseous pollutants and ˜25% of total PM10 in the entire city. Although vehicle use intensity increased rapidly in Guangzhou during 2005-2009, vehicle emissions were estimated to have been reduced by 12% for CO, 21% for THC and 20% for PM10 relative to those in 2005. NOx emissions were estimated to have remained almost constant during this period. Compared to the "without control" scenario, 19% (15%-23%) of CO, 20% (18%-23%) of THC, 9% (8%-10%) of NOx and 16% (12%-20%) of PM10 were estimated to have been mitigated from a combination of the implementation of Euro III standards for light-duty vehicles (LDVs) and heavy-duty diesel vehicles and improvement of fuel quality. This study also evaluated several enhanced vehicle emission control actions taken recently. For example, the enhanced I/M program for LDVs was estimated to reduce 11% (9%-14%) of CO, 9% (8%-10%) of THC and 2% (2%-3%) of NOx relative to total vehicle emissions in 2009. Total emission reductions by temporary traffic controls for the Asian Games were estimated equivalent to 9% (7%-11%) of CO, 9% (8%-10%) of THC, 5% (5%-6%) of NOx and 10% (8%-13%) of PM10 estimated total vehicle emissions in 2009. Those controls are essential to further vehicle emission mitigation in Guangzhou required by the new National Ambient Air Quality Standards.

  17. 40 CFR 63.5870 - How do I calculate annual uncontrolled and controlled organic HAP emissions from my wet-out area...

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... table temperature) amongst all formulae. (You may use the results of the worst-case formula test for all..., conduct at least one test (consisting of three runs). During the test, track information on organic HAP... table. (6) Using the test results, develop uncontrolled and controlled organic HAP emissions...

  18. Catalog of total excitation-emission and total synchronous fluorescence maps with synchronous fluorescence spectra of homologated fluorescent pesticides in large use in Morocco: development of a spectrometric low cost and direct analysis as an alert method in case of massive contamination of soils and waters by fluorescent pesticides.

    PubMed

    Foudeil, S; Hassoun, H; Lamhasni, T; Ait Lyazidi, S; Benyaich, F; Haddad, M; Choukrad, M; Boughdad, A; Bounakhla, M; Bounouira, H; Duarte, R M B O; Cachada, A; Duarte, A C

    2015-05-01

    The purpose of this research is to develop a direct spectrometric approach to monitor soils and waters, at a lower cost than the widely used chromatographic techniques; a spectrometric approach that is effective, reliable, fast, easy to implement, and without any use of organic solvents whose utilization is subject to law limitation. It could be suitable at least as an alert method in case of massive contamination. Here, we present for the first time a catalog of excitation-emission and total synchronous fluorescence maps that may be considered as fingerprints of a series of homologated pesticides, in large use in Morocco, aiming at a direct detection of their remains in agricultural soils and neighboring waters. After a large survey among farmers, agricultural workers and product distributors in two important agricultural regions of Morocco (Doukkala-Abda and Sebou basin), 48 commercial pesticides, which are fluorescent, were chosen. A multi-component spectral database of these targeted commercial pesticides was elaborated. For each pesticide, dissolved in water at the lowest concentration giving a no-noise fluorescence spectrum, the total excitation-emission matrix (TEEM), the total synchronous fluorescence matrix (TSFM) in addition to synchronous fluorescence spectra (SFS) at those offsets giving the highest fluorescence intensity were recorded. To test this preliminary multi-component database, two real soil samples, collected at a wheat field and at a vine field in the region of Doukkala, were analyzed. Remains of the commercial Pirimor (Carbamate) and Atlantis (Sulfonylurea) were identified by comparison of the recorded TEEM, TSFM, and SFS to those of the preliminary catalog at one hand, and on the basis of the results of a field pre-survey. The developed approach seems satisfactory, and the fluorimetric fingerprint database is under extension to a higher number of fluorescent pesticides in common use among the Moroccan agricultural regions. PMID:25424031

  19. Effects of a perennial ryegrass diet or total mixed ration diet offered to spring-calving Holstein-Friesian dairy cows on methane emissions, dry matter intake, and milk production.

    PubMed

    O'Neill, B F; Deighton, M H; O'Loughlin, B M; Mulligan, F J; Boland, T M; O'Donovan, M; Lewis, E

    2011-04-01

    The objective of the present study was to compare the enteric methane (CH4) emissions and milk production of spring-calving Holstein-Friesian cows offered either a grazed perennial ryegrass diet or a total mixed ration (TMR) diet for 10 wk in early lactation. Forty-eight spring-calving Holstein-Friesian dairy cows were randomly assigned to 1 of 2 nutritional treatments for 10 wk: 1) grass or 2) TMR. The grass group received an allocation of 17 kg of dry matter (DM) of grass per cow per day with a pre-grazing herbage mass of 1,492 kg of DM/ha. The TMR offered per cow per day was composed of maize silage (7.5 kg of DM), concentrate blend (8.6 kg of DM), grass silage (3.5 kg of DM), molasses (0.7 kg of DM), and straw (0.5 kg of DM). Daily CH4 emissions were determined via the emissions from ruminants using a calibrated tracer technique for 5 consecutive days during wk 4 and 10 of the study. Simultaneously, herbage dry matter intake (DMI) for the grass group was estimated using the n-alkane technique, whereas DMI for the TMR group was recorded using the Griffith Elder feeding system. Cows offered TMR had higher milk yield (29.5 vs. 21.1 kg/d), solids-corrected milk yield (27.7 vs. 20.1 kg/d), fat and protein (FP) yield (2.09 vs. 1.54 kg/d), bodyweight change (0.54 kg of gain/d vs. 0.37 kg of loss/d), and body condition score change (0.36 unit gain vs. 0.33 unit loss) than did the grass group over the course of the 10-wk study. Methane emissions were higher for the TMR group than the grass group (397 vs. 251 g/cow per day). The TMR group also emitted more CH4 per kg of FP (200 vs. 174 g/kg of FP) than did the grass group. They also emitted more CH4 per kg of DMI (20.28 vs. 18.06 g/kg of DMI) than did the grass group. In this study, spring-calving cows, consuming a high quality perennial ryegrass diet in the spring, produced less enteric CH4 emissions per cow, per unit of intake, and per unit of FP than did cows offered a standard TMR diet. PMID:21426985

  20. Twenty-five years of continuous sulphur dioxide emission reduction in Europe

    NASA Astrophysics Data System (ADS)

    Vestreng, V.; Myhre, G.; Fagerli, H.; Reis, S.; Tarrasón, L.

    2007-07-01

    During the last twenty-five years European emission data have been compiled and reported under the Cooperative Programme for Monitoring and Evaluation of the Long-range Transmission of Air Pollutants in Europe (EMEP) as part of the work under the UNECE Convention on Long-range Transboundary Air Pollution (LRTAP). This paper presents emission trends of SO2 reported to EMEP and validated within the programme for the period 1980-2004. These European anthropogenic sulphur emissions have been steadily decreasing over the last twenty-five years, amounting from about 55 Tg SO2 in 1980 to 15 Tg SO2 in 2004. The uncertainty in sulphur emission estimates for individual countries and years are documented to range between 3% and 25%. The relative contribution of European emissions to global anthropogenic sulphur emissions has been halved during this period. Based on annual emission reports from European countries, three emission reduction regimes have been identified. The period 1980-1989 is characterized by low annual emission reductions (below 5% reduction per year and 20% for the whole period) and is dominated by emission reductions in Western Europe. The period 1990-1999 is characterised by high annual emission reductions (up to 11% reduction per year and 54% for the whole period), most pronounced in Central and Eastern Europe. The annual emission reductions in the period 2000-2004 are medium to low (below 6% reduction per year and 17% for the whole period) and reflect the unified Europe, with equally large reductions in both East and West. The sulphur emission reduction has been largest in the sector Combustion in energy and transformation industries, but substantial decreases are also seen in the Non-industrial combustion plants together with the sectors Industrial combustion and Industrial production processes. The majority of European countries have reduced their emissions by more than 60% between 1990 and 2004, and one quarter have already achieved sulphur emission reductions higher than 80%. At European level, the total sulphur target for 2010 set in the Gothenburg Protocol (16 Tg) has apparently already been met by 2004. However, still half of the Parties to the Gothenburg Protocol have to reduce further their sulphur emissions in order to attain their individual country total emission targets for 2010. It is also noteworthy that, contrasting the Gothenburg Protocol requirements, a growing number of countries have recently been reporting increasing sulphur emissions, while others report only minor further decreases. The emission trends presented here are supported by different studies of air concentrations and depositions carried out within and outside the framework of the LRTAP Convention.

  1. Twenty-five years of continuous sulphur dioxide emission reduction in Europe

    NASA Astrophysics Data System (ADS)

    Vestreng, V.; Myhre, G.; Fagerli, H.; Reis, S.; Tarrasón, L.

    2007-04-01

    During the last twenty-five years European emission data have been compiled and reported under the Cooperative Programme for Monitoring and Evaluation of the Long-range Transmission of Air Pollutants in Europe (EMEP) as part of the work under the UNECE Convention on Long-range Transboundary Air Pollution (LRTAP). This paper presents emission trends of SO2 reported to EMEP and validated within the programme for the period 1980-2004. These European anthropogenic sulphur emissions have been steadily decreasing over the last twenty-five years, amounting from about 55 Tg SO2 in 1980 to 15 Tg SO2 in 2004. The uncertainty in sulphur emission estimates for individual countries and years are documented to range between 3% and 25%. The relative contribution of European emissions to global anthropogenic sulphur emissions has been halved during this period. Based on annual emission reports from European countries, three emission reduction regimes have been identified. The period 1980-1989 is characterized by low annual emission reductions (below 5% reduction per year and 20% for the whole period) and is dominated by emission reductions in Western Europe. The period 1990-1999 is characterised by high annual emission reductions (up to 11% reduction per year and 54% for the whole period), most pronounced in Central and Eastern Europe. The annual emission reductions in the period 2000-2004 are medium to low and reflect the unified Europe, with equally large reductions in both East and West. The sulphur emission reduction has been largest in the sector Combustion in energy and transformation industries, but substantial decreases are also seen in the Non-industrial combustion plants together with the sectors Industrial Combustion and Industrial Production Processes. The majority of European countries have reduced their emissions by more than 60% between 1990 and 2004, and one quarter have already achieved sulphur emission reductions higher than 80%. At European level, the total sulphur target for 2010 set in the Gothenburg Protocol (16 Tg) has apparently already been met by 2004. However, still half of the Parties to the Gothenburg Protocol have to reduce further their sulphur emissions in order to attain their individual country total emission targets for 2010. It is also noteworthy that, contrasting the Gothenburg Protocol requirements, a growing number of countries have recently been reporting increasing sulphur emissions, while others report only minor further decreases. The emission trends presented here are supported by different studies of air concentrations and depositions carried out within and outside the framework of the LRTAP Convention.

  2. Estimation of vehicular emissions using dynamic emission factors: A case study of Delhi, India

    NASA Astrophysics Data System (ADS)

    Mishra, Dhirendra; Goyal, P.

    2014-12-01

    The estimation of vehicular emissions depends mainly on the values of emission factors, which are used for the development of a comprehensive emission inventory of vehicles. In this study the variations of emission factors as well as the emission rates have been studied in Delhi. The implementation of compressed natural gas (CNG), in the diesel and petrol, public vehicles in the year 2001 has changed the complete air quality scenario of Delhi. The dynamic emission factors of criteria pollutants viz. carbon monoxide (CO), nitrogen oxide (NOx) and particulate matter (PM10) for all types of vehicles have been developed after, which are based on the several factors such as regulated emission limits, number of vehicle deterioration, vehicle increment, vehicle age etc. These emission factors are found to be decreased continuously throughout the study years 2003-2012. The International Vehicle Emissions (IVE) model is used to estimate the emissions of criteria pollutants by utilizing a dataset available from field observations at different traffic intersections in Delhi. Thus the vehicular emissions, based on dynamic emission factors have been estimated for the years 2003-2012, which are found to be comparable with the monitored concentrations at different locations in Delhi. It is noticed that the total emissions of CO, NOx, and PM10 are increased by 45.63%, 68.88% and 17.92%, respectively up to the year 2012 and the emissions of NOx and PM10 are grown continuously with an annual average growth rate of 5.4% and 1.7% respectively.

  3. Carbon emissions from spring 1998 fires in tropical Mexico

    SciTech Connect

    Cairns, M.A.; Hao, W.M.; Alvarado, E.; Haggerty, P.K.

    1999-04-01

    The authors used NOAA-AVHRR satellite imagery, biomass density maps, fuel consumption estimates, and a carbon emission factor to estimate the total carbon (C) emissions from the Spring 1998 fires in tropical Mexico. All eight states in southeast Mexico were affected by the wildfires, although the activity was concentrated near the common border of Oaxaca, Chiapas, and Veracruz. The fires burned approximately 482,000 ha and the land use/land cover classes most extensively impacted were the tall/medium selvas (tropical evergreen forests), open/fragmented forests, and perturbed areas. The total prompt emissions were 4.6 TgC during the two-month period of the authors` study, contributing an additional 24% to the region`s average annual net C emissions from forestry and land-use change. Mexico in 1998 experienced its driest Spring since 1941, setting the stage for the widespread burning.

  4. CO2 emissions from German drinking water reservoirs estimated from routine monitoring data

    NASA Astrophysics Data System (ADS)

    Saidi, H.; Koschorreck, M.

    2016-01-01

    Globally, reservoirs are a significant source of atmospheric CO2. However, precise quantification of greenhouse gas emissions from drinking water reservoirs on the regional or national scale is still challenging. We calculated CO2 fluxes for 39 German drinking water reservoirs during a period of 22 years (1991-2013) using routine monitoring data in order to quantify total emission of CO2 from drinking water reservoirs in Germany. All reservoirs were small net CO2 sources with a median flux of 167 g C m-2 y-1, which makes gaseous emissions a relevant process for the reservoirs carbon budgets. In total, German drinking reservoirs emit 44000 t of CO2 annually, which makes them a negligible CO2 source in Germany. Fluxes varied seasonally with median fluxes of 30, 11, and 46 mmol m-2 d-1 in spring, summer, and autumn respectively. Differences between reservoirs appeared to be primarily caused by the concentration of CO2 in the surface water rather than by the physical gas transfer coefficient. Consideration of short term fluctuations of the gas transfer coefficient due to variable wind had only a minor effect on the annual budgets. High CO2 emission only occurred in reservoirs with pH < 7 and total alkalinity < 0.2 mEq l-1. Annual CO2 emission correlated exponentially with pH, making pH a suitable proxy for CO emission from German drinking water reservoirs.

  5. Annual maximum 5-day rainfall total and maximum number of consecutive dry days over Central America and the Caribbean in the late twenty-first century projected by an atmospheric general circulation model with three different horizontal resolutions

    NASA Astrophysics Data System (ADS)

    Nakaegawa, T.; Kitoh, A.; Murakami, H.; Kusunoki, S.

    2014-04-01

    We simulated changes in annual maximum 5-day rainfall (RX5D) and annual maximum number of consecutive dry days (CDD) in Central America, Mexico, and the Caribbean with three different horizontal resolution atmospheric global general circulation models (AGCMs) and quantified the uncertainty of the projections. The RX5Ds and CDDs were projected to increase in most areas in response to global warming. However, consistent changes were confined to small areas: for RX5D, both coastal zones of northern Mexico and the Yucatan Peninsula; for CDD, the Pacific coastal zone of Mexico, the Yucatan Peninsula, and Guatemala. All three AGCMs projected that RX5Ds and CDDs averaged over only the land area and over the entire area (land and ocean) would increase. The dependence of RX5D probability density functions on the horizontal resolutions was complex. Precipitation unrelated to tropical cyclones was primarily responsible for the projected increases in the frequency of RX5Ds greater than 300 mm.

  6. 76 FR 69239 - Annual Retail Trade Survey

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-11-08

    ... survey, the Census Bureau will collect data covering annual sales, annual e-commerce sales, year-end... receivables, and, for selected industries, merchandise line sales, and percent of e-commerce sales to..., annual e-commerce sales, purchases, total operating expenses, accounts receivables, and...

  7. The wildland fire emission inventory: western United States emission estimates and an evaluation of uncertainty

    NASA Astrophysics Data System (ADS)

    Urbanski, S. P.; Hao, W. M.; Nordgren, B.

    2011-12-01

    Biomass burning emission inventories serve as critical input for atmospheric chemical transport models that are used to understand the role of biomass fires in the chemical composition of the atmosphere, air quality, and the climate system. Significant progress has been achieved in the development of regional and global biomass burning emission inventories over the past decade using satellite remote sensing technology for fire detection and burned area mapping. However, agreement among biomass burning emission inventories is frequently poor. Furthermore, the uncertainties of the emission estimates are typically not well characterized, particularly at the spatio-temporal scales pertinent to regional air quality modeling. We present the Wildland Fire Emission Inventory (WFEI), a high resolution model for non-agricultural open biomass burning (hereafter referred to as wildland fires, WF) in the contiguous United States (CONUS). The model combines observations from the MODerate Resolution Imaging Spectroradiometer (MODIS) sensors on the Terra and Aqua satellites, meteorological analyses, fuel loading maps, an emission factor database, and fuel condition and fuel consumption models to estimate emissions from WF. WFEI was used to estimate emissions of CO (ECO) and PM2.5 (EPM2.5) for the western United States from 2003-2008. The uncertainties in the inventory estimates of ECO and EPM2.5 (uECO and uEPM2.5, respectively) have been explored across spatial and temporal scales relevant to regional and global modeling applications. In order to evaluate the uncertainty in our emission estimates across multiple scales we used a figure of merit, the half mass uncertainty, ũEX (where X = CO or PM2.5), defined such that for a given aggregation level 50% of total emissions occurred from elements with uEX ũEX. The sensitivity of the WFEI estimates of ECO and EPM2.5 to uncertainties in mapped fuel loading, fuel consumption, burned area and emission factors have also been examined. The estimated annual, domain wide ECO ranged from 436 Gg yr-1 in 2004 to 3107 Gg yr-1 in 2007. The extremes in estimated annual, domain wide EPM2.5 were 65 Gg yr-1 in 2004 and 454 Gg yr-1 in 2007. Annual WF emissions were a significant share of total emissions from non-WF sources (agriculture, dust, non-WF fire, fuel combustion, industrial processes, transportation, solvent, and miscellaneous) in the western United States as estimated in a national emission inventory. In the peak fire year of 2007, WF emissions were ~20% of total (WF + non-WF) CO emissions and ~39% of total PM2.5 emissions. During the months with the greatest fire activity, WF accounted for the majority of total CO and PM2.5 emitted across the study region. Uncertainties in annual, domain wide emissions was 28% to 51% for CO and 40% to 65% for PM2.5. Sensitivity of ũECO and ũEPM2.5 to the emission model components depended on scale. At scales relevant to regional modeling applications (Δx = 10 km, Δt = 1 day) WFEI estimates 50% of total ECO with an uncertainty <133% and half of total EPM2.5 with an uncertainty <146%. ũECO and ũEPM2.5 are reduced by more than half at the scale of global modeling applications (Δ x = 100 km, Δ t = 30 day) where 50% of total emissions are estimated with an uncertainty <50% for CO and <64% for PM2.5. Uncertainties in the estimates of burned area drives the emission uncertainties at regional scales. At global scales ũECO is most sensitive to uncertainties in the fuel load consumed while the uncertainty in the emission factor for PM2.5 plays the dominant role in ũEPM2.5. Our analysis indicates that the large scale aggregate uncertainties (e.g. the uncertainty in annual CO emitted for CONUS) typically reported for biomass burning emission inventories may not be appropriate for evaluating and interpreting results of regional scale modeling applications that employ the emission estimates. When feasible, biomass burning emission inventories should be evaluated and reported across the scales for which they are intended to be used.

  8. Carbon dioxide emissions from an Acacia plantation on peatland in Sumatra, Indonesia

    NASA Astrophysics Data System (ADS)

    Jauhiainen, J.; Hooijer, A.; Page, S. E.

    2011-08-01

    Peat surface CO2 emission, groundwater table depth and peat temperature were monitored for two years along transects in an Acacia plantation on thick tropical peat (>4 m) in Sumatra, Indonesia. A total of 2300 emission measurements were taken at 144 locations. The autotrophic root respiration component of the CO2 emission was separated from heterotrophic emissions caused by peat oxidation in three ways: (i) by comparing CO2 emissions within and beyond the tree rooting zone, (ii) by comparing CO2 emissions with and without peat trenching (i.e. cutting any roots remaining in the peat beyond the tree rooting zone), and (iii) by comparing CO2 emissions before and after Acacia tree harvesting. On average, the contribution of root respiration to daytime CO2 emission is 21 % along transects in mature tree stands. At locations 0.5 m from trees this is up to 80 % of the total emissions, but it is negligible at locations more than 1.3 m away. This means that CO2 emission measurements well away from trees are free of any root respiration contribution and thus represent only peat oxidation emission. We find daytime mean annual CO2 emission from peat oxidation alone of 94 t ha-1 yr-1 at a mean water table depth of 0.8 m, and a minimum emission value of 80 t ha-1 yr-1 after correction for the effect of diurnal temperature fluctuations, which resulted in a 14.5 % reduction of the daytime emission. There is a positive correlation between mean long-term water table depths and peat oxidation CO2 emission. However, no such relation is found for instantaneous emission/water table depth within transects and it is clear that factors other than water table depth also affect peat oxidation and total CO2 emissions. The increase in the temperature of the surface peat due to plantation development may explain over 50 % of peat oxidation emissions.

  9. Estimation of atmospheric emissions of six semivolatile polycyclic aromatic hydrocarbons in southern canada and the United States by use of an emissions processing system.

    PubMed

    Galarneau, Elisabeth; Makar, Paul A; Sassi, Mourad; Diamond, Miriam L

    2007-06-15

    Polycyclic aromatic hydrocarbons (PAHs) are toxic compounds that are ubiquitous in the atmospheric environment. The input for an emissions processing system that was originally configured forthe study of criteria air pollutants was updated to calculate emissions of six semivolatile PAHs. The goal of the work was to produce emissions estimates with the spatial and temporal resolution needed to serve as input to a regional air quality model for southern Canada and the U.S. Such modeling is helpful in determining reductions in PAH emissions that may be necessary to protect human and ecosystem health. The total annual emission of the six PAHs (sigma6PAH) for both countries was estimated at 18 273 Mg/year. A total of 90% of these emissions arise from U.S. sources. The top six source types account for 73% of emissions and are related to metal production, open burning, incineration, and forest fires. The emission factors used in this study were derived from published compilations. Although this approach has the advantage of quality control during the compilation process, some compilations include factors from older studies that may overestimate emissions since they do not account for recent improvements in emission control technology. When compared to estimates published in the National Emissions Inventory (NEI) for 2002, the U.S. emissions in this study are higher by a factor of 4 (16 424 vs 4102 Mg/year). The cause of this difference has been investigated, and much of it is likely due to our use of data unavailable in the 2002 NEI but inferred here on the basis of the PAH emissions literature. Augmenting the 2002 NEI with this additional information would bring its reported annual emissions to 8213 Mg/year, which is within a factor of 2 of the estimates herein. The results presented for southern Canada are the first published values for all known PAH sources in that country. PMID:17626414

  10. Development of a high-resolution (1 km × 1 km, 1 h) emission model for Spain: The High-Elective Resolution Modelling Emission System (HERMES)

    NASA Astrophysics Data System (ADS)

    Baldasano, José María; Güereca, Leonor Patricia; López, Eugeni; Gassó, Santiago; Jimenez-Guerrero, Pedro

    This work presents the results of the development and application of the High-Elective Resolution Modelling Emission System (HERMES). HERMES generates the emissions for Spain needed for the application of high-resolution chemistry transport models, taking the year 2004 as reference with a temporal resolution of 1 h and a spatial resolution of 1 km 2 considering both anthropogenic (power generation, industrial activities, on-road traffic, ports, airports, solvent use, domestic and commercial fossil fuel use) and biogenic sources (vegetation), using a bottom-up approach, up-to-date information and state-of-the-art methodologies for emission estimation. HERMES is capable of calculating emissions by sector-specific sources or by individual installations and stacks. The annual addition of hourly sectorial emissions leads to an estimation of total annual emissions as follows: NO x, 795 kt; NMVOCs, 1025 kt; CO, 1236 kt; SO 2, 1142 kt and TSP, 180 kt; which are distributed principally in the greater areas of the main cities, highways and large point sources. NO x, SO 2 and PM 2.5 highly correlate with the power generation by coal use, achieving higher emission levels during summertime due to the increase of electricity demand by cooling systems. NMVOCs show high correlation with temperature and solar radiation (mainly as a consequence of the important weight of biogenic emissions) causing the maximum emissions during the daylight hours of summer months. CO emissions are mostly influenced by the on-road traffic; consequently the higher emissions are attained in summer because of the increase of daily average traffic during holidays. The most significant total emission sources are on-road traffic (38%), combustion in power generation plants (33%), biogenic sources (12%) and combustion in manufacturing industries (9%). The inventory generated with HERMES emission model has been successfully integrated within the Spanish Ministry of the Environment's air quality forecasting system (Caliope project), being the emission core for the validation and assessment of air quality simulations in Spain.

  11. Carbonyl emissions from commercial cooking sources in Hong Kong.

    PubMed

    Ho, Steven Sai Hang; Yu, Jian Zhen; Chu, Kam Wah; Yeung, Lam Lung

    2006-08-01

    Cooking fumes are an important carbonyl emission source, especially in a highly urbanized city, such as Hong Kong. Cooking exhaust from 15 commercial kitchens of a variety of cooking styles was sampled and analyzed for a suite of 13 carbonyl compounds. Carbonyl compositions were varied among the different cooking styles. Formaldehyde was generally the most abundant carbonyl, and its contribution to the total carbonyl amount on a molar basis ranged from 12 to 60%. Acrolein was also found to be an abundant carbonyl in the cooking exhaust. The highest contribution by acrolein to the total carbonyls was found to be 30% in the exhaust of a western-style steak restaurant. Long-chain saturated carbonyls, that is, heptanal, octanal, and nonanal, accounted for a significant fraction (> 40%) of the total carbonyls in kitchens that always used heated cooking oils. Two dicarbonyls, glyoxal and methylglyoxal, had a various presence in the cooking emissions, ranging from negligible to 10%. The presence of benzaldehyde and tolualdehyde was mostly negligible in the sampled kitchen exhaust. Annual emission rates of both individual carbonyls and total carbonyls were estimated for various types of commercial kitchens. Local-style fast-food shops contributed the highest total carbonyl emissions per year mainly because of the large number of this kind of restaurant in Hong Kong. The citywide annual emission rates of the three most toxic carbonyls, formaldehyde, acetaldehyde, and acrolein, were estimated assuming that the limited number of sampled restaurants were representative of the average restaurants. Such estimates of carbonyl emission rates were comparable to the estimated carbonyl emissions from vehicular sources, suggesting the importance of commercial cooking as a source for carbonyls in Hong Kong. PMID:16933641

  12. The emission density and trend of ammonia over China

    SciTech Connect

    Wen-Xing Wang; Xiao-Feng Lu; Yan-Bo Pang; Tao Wang

    1996-12-31

    Nationwide, province-based and gridded anthropogenic NH{sub 3} emissions in China have been made based on the number of livestock, poultry, fertilizer application, NH{sub 3} production and human beings. The total annual emissions have been calculated to be 89194.4 kt in 1991. In which livestock, fertilizer application, human beings, poultry and NH{sub 3} production account for 56.8%, 17.5%, 16.7% and 0.9% respectively. The gridded emission densities show that the high densities have appeared in the Middle Eastern China and Sichuan Basin. The average emission density over China is 0.9 t/km{sup 2} a in 1991. Which is just less than that of Europe (1.1 t/km{sup 2} a). The emission trends of NH{sub 3} have also been calculated from 1991 to 1992.

  13. Emissions of gaseous and particulate pollutants in a port and harbour region in India.

    PubMed

    Gupta, A K; Patil, R S; Gupta, S K

    2002-12-01

    Ports can generate large quantity of pollutants in the atmosphere due to various activities like loading and unloading, transportation, and construction operations. Determination of the character and quantity of emissions from individual sources is an essential step in any project to control and minimize the emissions. In this study a detailed emission inventory of total suspended particulate matter (TSP), particulate matter less than 10 microm (PM10), sulfur dioxide (SO2) and nitrogen oxides (NOx) for a port and harbour project near Mumbai is compiled. Results show that the total annual average contributions of TSP and PM10 from all the port activities were 872 and 221 t yr(-1), respectively. Annual average emissions of gaseous pollutants SO2 and NOx were 56 and 397 t yr(-1), respectively, calculated by using emission factors for different port activities. The maximum TSP emission (419 t yr(-1)) was from paved roads, while the least (0.4 t yr(-1)) was from bulk handling activity. The maximum PM10 emission (123 t yr(-1)) was from unpaved roads and minimum (0.2 t yr(-1)) from bulk handling operations. Similarly the ratio of TSP and PM10 emission was highest (5.18) from paved roads and least (2.17) from bulk handling operations. Regression relation was derived from existing emission data of TSP and PM10 from various port activities. Good correlation was observed between TSP and PM10 having regression coefficient >0.8. PMID:12449324

  14. Emissions of Trace Gases and Particles from Two Ships in the Southern Atlantic Ocean

    NASA Technical Reports Server (NTRS)

    Sinha, Parikhit; Hobbs, Peter V.; Yokelson, Robert J.; Christian, Ted J.; Kirchstetter, Thomas W.; Bruintjes, Roelof

    2003-01-01

    Measurements were made of the emissions of particles and gases from two diesel-powered ships in the southern Atlantic Ocean off the coast of Namibia. The measurements are used to derive emission factors from ships of three species not reported previously, namely, black carbon, accumulation-mode particles, and cloud condensation nuclei (CCN), as well as for carbon dioxide, carbon monoxide (CO), methane (CH4), non-methane hydrocarbons, sulfur dioxide (SO2), nitrogen oxides (NOx), and condensation nuclei. The effects of fuel grade and engine power on ship emissions are discussed. The emission factors are combined with fuel usage data to obtain estimates of global annual emissions of various particles and gases from ocean-going ships. Global emissions of black carbon, accumulation- mode particles, and CCN from ocean-going ships are estimated to be 19-26 Gg yr(sup -1), (4.4-6.1) x 10(exp 26) particles yr(sup -1), and (1.0-1.5) x l0(exp 26) particles yr(sup -1), respectively. Black carbon emissions from ocean-going ships are approximately 0.2% of total anthropogenic emissions. Emissions of NOx and SO2 from ocean-going ships are approximately 10-14% and approximately 3-4%, respectively, of the total emissions of these species from the burning of fossil fuels, and approximately 40% and approximately 70%, respectively, of the total emissions of these species from the burning of biomass. Global annual emissions of CO and CH4 from ocean-going ships are approximately 2% and approximately 2-5%, respectively, of natural oceanic emissions of these species.

  15. LLNL NESHAPs 2003 Annual Report

    SciTech Connect

    Harrach, R J; Gallegos, G M; Peterson, S; Wilson, K R; Althouse, P E; Larson, J M; Bertoldo, N A; Tate, P J; Bowen, B

    2004-06-23

    This annual report is prepared pursuant to the National Emission Standards for Hazardous Air Pollutants (NESHAPs; Title 40 Code of Federal Regulations [CFR] Part 61, Subpart H). Subpart H governs radionuclide emissions to air from Department of Energy (DOE) facilities. NESHAPs limits the emission of radionuclides to the ambient air from DOE facilities to levels resulting in an annual effective dose equivalent (EDE) of 10 mrem (100 {micro}Sv) to any member of the public. The EDEs for the Lawrence Livermore National Laboratory (LLNL) site-wide maximally exposed members of the public from operations in 2003 are summarized here. Livermore site: 0.044 mrem (0.44 {micro}Sv) (55% from point-source emissions, 45% from diffuse-source emissions). The point-source emissions include gaseous tritium modeled as tritiated water vapor as directed by EPA Region IX; the resulting dose is used for compliance purposes. Site 300: 0.017 mrem (0.17 {micro}Sv) (98% from point-source emissions, 2% from diffuse-source emissions). The EDEs were calculated using the EPA-approved CAP88-PC air dispersion/dose-assessment model, except for doses for two diffuse sources that were estimated using measured concentrations and dose coefficients. Site specific meteorological data, stack flow data, and emissions estimates based on radionuclide usage inventory data or continuous stack monitoring data were the specific inputs to CAP88-PC for each modeled source.

  16. LLNL NESHAPs 2002 Annual Report

    SciTech Connect

    Harrach, R J; Gallegos, G M; Peterson, S-R; Tate, P J; Bertoldo, N A; Wilson, K R; Althouse, P E; Larson, J M

    2003-06-01

    This annual report is prepared pursuant to the National Emission Standards for Hazardous Air Pollutants (NESHAPs; Title 40 Code of Federal Regulations [CFR] Part 61, Subpart H). Subpart H governs radionuclide emissions to air from Department of Energy (DOE) facilities. NESHAPs limits the emission of radionuclides to the ambient air from DOE facilities to levels resulting in an annual effective dose equivalent (EDE) of 10 mrem (100 {micro}Sv) to any member of the public. The EDEs for the Lawrence Livermore National Laboratory (LLNL) site-wide maximally exposed members of the public from operations in 2002 are summarized here: (1) Livermore site: 0.023 mrem (0.23 {micro}Sv) (43% from point-source emissions, 57% from diffuse-source emissions). The point-source emissions include gaseous tritium modeled as tritiated water vapor as directed by EPA Region IX; the resulting dose is used for compliance purposes; and (2) Site 300: 0.021 mrem (0.21 {micro}Sv) (85% from point-source emissions, 15% from diffuse-source emissions). The EDEs were calculated using the EPA-approved CAP88-PC air dispersion/dose-assessment model, except for doses for three diffuse sources, which were calculated from measured concentrations and dose coefficients. Site specific meteorological data, stack flow data, and emissions estimates based on radionuclide usage inventory data or continuous stack monitoring data were the specific inputs to CAP88-PC for each modeled source.

  17. Development of an emission factor for ammonia emissions from US swine farms based on field tests and application of a mass balance method

    NASA Astrophysics Data System (ADS)

    Doorn, M. R. J.; Natschke, D. F.; Thorneloe, S. A.; Southerland, J.

    This paper discusses and summarizes post-1994 US and European information on ammonia (NH 3) emissions from swine farms and assesses the applicability for general use in the United States. The emission rates for the houses calculated by various methods show good agreement and suggest that the houses are a more significant source than previously thought. A general emission factor for houses of 3.7±1.0 kg NH 3/ year/ finisher pig or 59±10 g NH 3/kg live weight/year is recommended. For lagoons, it was found that there is good similarity between the field test results and the number calculated by a mass balance method. The suggested annual NH 3 emission factor for lagoons based on field tests at one swine farm lagoon in North Carolina is 2.4 kg/ year/ pig. Emission rates from sprayfields were estimated using a total mass balance approach, while subtracting the house and lagoon emissions. The total emission rates for finishing pigs at the test farm compared well to the total rate established by a mass balance approach based on nitrogen intake and volatilization. Therefore, it was concluded that a mass balance approach can be helpful in estimating NH 3 emissions from swine farms. A general emission factor of 7±2 kg NH 3/pig/year could be developed, which is comparable to general European emission factors, which varied from 4.8 to 6.4 kg NH 3/pig/year.

  18. Estimation of atmospheric emissions of six semivolatile polycyclic aromatic hydrocarbons in southern Canada and the United States by use of an emissions processing system

    SciTech Connect

    Elisabeth Galarneau; Paul A. Makar; Mourad Sassi; Miriam L. Diamond

    2007-06-15

    Polycyclic aromatic hydrocarbons (PAHs) are toxic compounds that are ubiquitous in the atmospheric environment. The input for an emissions processing system that was originally configured for the study of criteria air pollutants was updated to calculate emissions of six semivolatile PAHs. The goal of the work was to produce emissions estimates with the spatial and temporal resolution needed to serve as input to a regional air quality model for southern Canada and the U.S. The total annual emission of the six PAHs ({Sigma}6PAH) for both countries was estimated at 18,273 Mg/year. A total of 90% of these emissions arise from U.S. sources. The top six source types account for 73% of emissions and are related to metal production, open burning, incineration, and forest fires. Other sources include coal-fired boilers, diesel and gasoline vehicles, oxygen furnaces, and iron sintering. The emission factors used in this study were derived from published compilations. Although this approach has the advantage of quality control during the compilation process, some compilations include factors from older studies that may overestimate emissions since they do not account for recent improvements in emission control technology. When compared to estimates published in the National Emissions Inventory (NEI) for 2002, the U.S. emissions in this study are higher by a factor of 4. Much of the difference is likely due to use of data unavailable in the 2002 NEI but inferred here on the basis of the PAH emissions literature. Augmenting the 2002 NEI with this additional information would bring its reported annual emissions to 8213 Mg/year, which is within a factor of 2 of the estimates made by the authors. 17 refs., 5 figs., 2 tabs.

  19. Linking annual N2O emission in organic soils to mineral nitrogen input as estimated by heterotrophic respiration and soil C/N ratio.

    PubMed

    Mu, Zhijian; Huang, Aiying; Ni, Jiupai; Xie, Deti

    2014-01-01

    Organic soils are an important source of N2O, but global estimates of these fluxes remain uncertain because measurements are sparse. We tested the hypothesis that N2O fluxes can be predicted from estimates of mineral nitrogen input, calculated from readily-available measurements of CO2 flux and soil C/N ratio. From studies of organic soils throughout the world, we compiled a data set of annual CO2 and N2O fluxes which were measured concurrently. The input of soil mineral nitrogen in these studies was estimated from applied fertilizer nitrogen and organic nitrogen mineralization. The latter was calculated by dividing the rate of soil heterotrophic respiration by soil C/N ratio. This index of mineral nitrogen input explained up to 69% of the overall variability of N2O fluxes, whereas CO2 flux or soil C/N ratio alone explained only 49% and 36% of the variability, respectively. Including water table level in the model, along with mineral nitrogen input, further improved the model with the explanatory proportion of variability in N2O flux increasing to 75%. Unlike grassland or cropland soils, forest soils were evidently nitrogen-limited, so water table level had no significant effect on N2O flux. Our proposed approach, which uses the product of soil-derived CO2 flux and the inverse of soil C/N ratio as a proxy for nitrogen mineralization, shows promise for estimating regional or global N2O fluxes from organic soils, although some further enhancements may be warranted. PMID:24798347

  20. Inventory of emissions from non-automotive vehicular sources. Final report

    SciTech Connect

    Taback, H.J.; Macko, J.F.; Parker, N.R.; Dale, D.A.; Erlich, S.

    1980-02-01

    The report presents the results of a program to develop methodologies for the inventory of emissions from nonautomotive vehicular sources, which are applicable in all areas of California; and using these methods, compile an inventory of emissions for 1977 for the four counties comprising the South Coast Air Basin. In this study, nonautomotive vehicular sources were defined as construction equipment, farm vehicles, industrial vehicles, and small boats. The general approach was to determine total annual fuel consumption by vehicle type, then multiply each total by the appropriate EPA emission factors. For construction equipment, the method is based upon the level of construction activity, miles of roadway constructed, and human population. For farm vehicles, the method is based upon the annual number of harvested acres of each type of crop. For industrial vehicles, the method is based upon the vehicle population and usage factors. Boats are separated into pleasure and commercial categories, with usage and fuel consumption factors for each group.

  1. 12 CFR 1206.3 - Annual assessments.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... ratio to the total portion of the annual assessment allocated to the Enterprises that the total exposure... of the annual assessments based on the ratio between its minimum required regulatory capital and the.... Surplus funds shall be allocated to all Regulated Entities in the same proportion in which they...

  2. 12 CFR 1206.3 - Annual assessments.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... ratio to the total portion of the annual assessment allocated to the Enterprises that the total exposure... of the annual assessments based on the ratio between its minimum required regulatory capital and the.... Surplus funds shall be allocated to all Regulated Entities in the same proportion in which they...

  3. 12 CFR 1206.3 - Annual assessments.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... ratio to the total portion of the annual assessment allocated to the Enterprises that the total exposure... of the annual assessments based on the ratio between its minimum required regulatory capital and the.... Surplus funds shall be allocated to all Regulated Entities in the same proportion in which they...

  4. An emission inventory of sulfur from anthropogenic sources in Antarctica

    NASA Astrophysics Data System (ADS)

    Shirsat, S. V.; Graf, H. F.

    2009-05-01

    This paper presents first results of a comprehensive emission inventory of chemical species from anthropogenic activities (power generation, vehicles, ships and aircraft) in Antarctica, covering the 2004-2005 period. The inventory is based on estimated emission rates of fuel consumption provided by some of the Antarctic research stations. Since the emission sources have different modes of operation and use a variety of fuel, the emission flux rate of chemical species is calculated by multiplying the fuel consumption value with the density of fuel and appropriate emission factors. A separate inventory is prepared for each anthropogenic emission source in Antarctica. Depending on the type of operation, emission rates of SO2, and BC (Black Carbon, from shipping only) have been calculated using the above technique. However, only results of SO2 emissions from each source are presented here. Emission inventory maps of SO2 depicting the track/path taken by each mobile source are shown. The total annual SO2 is 158 Mg from power generation and vehicle operations, 3873 Mg from ships and 56 Mg from aircraft for 2004-2005 and these values undergo strong seasonality following the human activity in Antarctica. Though these figures are small when compared to the emissions at most other regions of the world, they are an indication that human presence in Antarctica leads to at least local pollution. The sources are mainly line and point sources and thus the local pollution potentially is relatively strong.

  5. An emission inventory of sulfur from anthropogenic sources in Antarctica

    NASA Astrophysics Data System (ADS)

    Shirsat, S. V.; Graf, H. F.

    2009-01-01

    This paper presents first results of a comprehensive emission inventory of chemical species from anthropogenic activities (power generation, vehicles, ships and aircraft) in Antarctica, covering the 2004-2005 period. The inventory is based on estimated emission rates of fuel consumption provided by some of the Antarctic research stations. Since the emission sources have different modes of operation and use a variety of fuel, the emission flux rate of chemical species is calculated by multiplying the fuel consumption value with the density of fuel and appropriate emission factors. A separate inventory is prepared for each anthropogenic emission source in Antarctica. Depending on the type of operation, emission rates of SO2, and BC (Black Carbon, from shipping only) have been calculated using the above technique. However, only results of SO2 emissions from each source are presented here. Emission inventory maps of SO2 depicting the track/path taken by each mobile source are shown. The total annual SO2 is 158 Mg from power generation and vehicle operations, 3873 Mg from ships and 56 Mg from aircraft for 2004-2005 and these values undergo strong seasonality following the human activity in Antarctica. Though these figures are small when compared to the emissions at most other regions of the world, they are an indication that human presence in Antarctica leads to at least local pollution. The sources are mainly line and point sources and thus the local pollution potentially is relatively strong.

  6. The impact of global aviation NOx emissions on tropospheric composition changes from 2005 to 2011

    NASA Astrophysics Data System (ADS)

    Wasiuk, D. K.; Khan, M. A. H.; Shallcross, D. E.; Lowenberg, M. H.

    2016-09-01

    The impact of aviation NOx emissions from 2005 to 2011 on the chemical composition of the atmosphere has been investigated on the basis of integrations of the 3-D global chemical and transport model, STOCHEM-CRI with the novel CRIv2-R5 chemistry scheme. A base case simulation without aircraft NOx emissions and integrations with NOx emissions from aircraft are inter-compared. The sensitivity of the global atmosphere to varying the quantity and the geographical distribution of the global annual aviation NOx emissions is assessed by performing, for the first time, a series of integrations based on changing the total mass and distribution of aircraft NOx emissions derived from air traffic movements recorded between 2005 and 2011. The emissions of NOx from the global fleet based on actual records of air traffic movements between 2005 and 2011 increased the global tropospheric annual mean burden of O3 by 1.0 Tg and decreased the global tropospheric annual mean burden of CH4 by 2.5 Tg. The net NOy and O3 production increases by 0.5% and 1%, respectively between 2005 and 2011 in total. At cruise altitude, the absolute increase in the modelled O3 mixing ratios is found to be up to 0.7 ppb between 2005 and 2011 at 25°N-50°N.

  7. Carbon emissions and sequestration in forests: Case studies from seven developing countries. Volume 4: Mexico: Draft

    SciTech Connect

    Makundi, W.; Sathaye, J.; Cerutti, O.M.; Ordonez, M.J.; Minjarez, R.D.

    1992-08-01

    Estimates of carbon emissions from deforestation in Mexico are derived for the year 1985 and for two contrasting scenarios in 2025. Carbon emissions are calculated through an in-depth review of the existing information on forest cover deforestation mtes and area affected by forest fires as well as on forests` carbon-related biological characteristics. The analysis covers both tropical -- evergreen and deciduous -- and temperate -- coniferous and broadleaf -- closed forests. Emissions from the forest sector are also compared to those from energy and industry. Different policy options for promoting the sustainable management of forest resources in the country are discussed. The analysis indicates that approximately 804,000 hectares per year of closed forests suffered from major perturbations in the mid 1980`s in Mexico, leading to an annual deforestation mte of 668,000 hectares. Seventy five percent of total deforestation is concentrated in tropical forests. The resulting annual carbon balance is estimated in 53.4 million tons per year, and the net committed emissions in 45.5 million tons or 41% and 38%, respectively, of the country`s total for 1985--87. The annual carbon balance from the forest sector in 2025 is expected to decline to 16.5 million tons in the low emissions scenario and to 22.9 million tons in the high emissions scenario. Because of the large uncertainties in some of the primary sources of information, the stated figures should be taken as preliminary estimates.

  8. Carbon emissions and sequestration in forests: Case studies from seven developing countries

    SciTech Connect

    Makundi, W.; Sathaye, J. ); Cerutti, O.M.; Ordonez, M.J.; Minjarez, R.D. Centro de Ecologia)

    1992-08-01

    Estimates of carbon emissions from deforestation in Mexico are derived for the year 1985 and for two contrasting scenarios in 2025. Carbon emissions are calculated through an in-depth review of the existing information on forest cover deforestation mtes and area affected by forest fires as well as on forests' carbon-related biological characteristics. The analysis covers both tropical -- evergreen and deciduous -- and temperate -- coniferous and broadleaf -- closed forests. Emissions from the forest sector are also compared to those from energy and industry. Different policy options for promoting the sustainable management of forest resources in the country are discussed. The analysis indicates that approximately 804,000 hectares per year of closed forests suffered from major perturbations in the mid 1980's in Mexico, leading to an annual deforestation mte of 668,000 hectares. Seventy five percent of total deforestation is concentrated in tropical forests. The resulting annual carbon balance is estimated in 53.4 million tons per year, and the net committed emissions in 45.5 million tons or 41% and 38%, respectively, of the country's total for 1985--87. The annual carbon balance from the forest sector in 2025 is expected to decline to 16.5 million tons in the low emissions scenario and to 22.9 million tons in the high emissions scenario. Because of the large uncertainties in some of the primary sources of information, the stated figures should be taken as preliminary estimates.

  9. Nitric oxide emission from a typical vegetable field in the Pearl River Delta, China

    NASA Astrophysics Data System (ADS)

    Li, Dejun; Wang, Xinming

    Croplands contribute to atmospheric nitric oxide (NO), but very limited data are available about NO fluxes from intensively managed croplands in China. In this study, NO fluxes were measured in a typical vegetable field planted with flowering Chinese cabbage ( Brassica campestris L. ssp. Chinensis var. utilis Tsen et Lee), which is the most widely cultivated vegetable in Guangdong province, south China. NO emission drastically increased after nitrogen fertilizer application, and other practices involving loosening the soil also enhanced NO emission. Mean NO emission flux was 47.5 ng N m -2 s -1 over a complete growth cycle. Annual NO emission from the vegetable field was about 10.1 kg N ha -1 yr -1. Fertilizer-induced NO emission factor was estimated to be 2.4%. Total NO emission from vegetable fields in Guangdong province was roughly estimated to be 11.7 Gg N yr -1 based on the vegetable field area and annual NO emission rate, and to be 13.3 Gg N yr -1 based on fertilizer-induced NO emission factor and background NO emission. This means that NO emission from vegetable fields was approximately 6% of NO x from commercial energy consumption in Guangdong province.

  10. Impacts of future climate change and emissions reductions on nitrogen and sulfur deposition over the United States

    NASA Astrophysics Data System (ADS)

    Tagaris, Efthimios; Liao, Kuo-Jen; Manomaiphiboon, Kasemsan; Woo, Jung-Hun; He, Shan; Amar, Praveen; Russell, Armistead G.

    2008-04-01

    Potential impacts of global climate change and emissions on the total nitrogen and sulfur deposition over the US are investigated. Three future years' annual average deposition rates (i.e., 2049-2051) are compared with historic ones (i.e., 2000-2002) accounting for existing US and individual State's emission regulations and strategies. Impacts of global climate change alone on regional nitrogen and sulfur deposition are small compared to impacts from emission control-related reductions for the projections used in this study. The combined effect of climate change and emission reductions is a decrease in the annual average nitrogen and sulfur deposition over the US. Reduced nitrogen species dominate oxidized nitrogen deposition in the future. Spatial distribution plots for both components show lower deposition rates in the future mainly in the middle and eastern States where reductions in NOx and SO2 emissions are more pronounced.

  11. Seasonal course of isoprene emissions from a midlatitude deciduous forest

    NASA Astrophysics Data System (ADS)

    Goldstein, Allen H.; Goulden, Michael L.; Munger, J. William; Wofsy, Steven C.; Geron, Christopher D.

    1998-12-01

    Continuous measurements of whole canopy isoprene emissions over an entire growing season are reported from Harvard Forest (4232'N, 7211'W). Emissions were calculated from the ratio of observed CO2 flux and gradient multiplied by the observed hydrocarbon gradients. In summer 1995, 24-hour average emissions of isoprene from June 1 through October 31 were 32.71010 molecules cm-2 s-l (mg C m-2 h-l = 2.8 1011 molecules cm-2 s-1), and the mean midday mixing ratio was 4.4 ppbv at 24 m. Isoprene emissions were zero at night, increased through the morning with increasing air temperature and light, reached a peak in the afternoon between the peaks in air temperature and light, and then declined with light. Isoprene emissions were observed over a shorter seasonal period than photosynthetic carbon uptake. Isoprene emission was not detected from young leaves and reached a peak rate (normalized for response to measured light and temperature conditions) 4 weeks after leaf out and 2 weeks after emissions began. The normalized emission rate remained constant for approximately 65 days, then decreased steadily through September and into October. Total isoprene emissions over the growing season (42 kg C ha-1 yr-1) were equal to 2% of the annual net uptake of carbon by the forest. Measured isoprene emissions were higher than the Biogenic Emission Inventory System-II model by at least 40% at midday and showed distinctly different diurnal and seasonal emission patterns. Seasonal adjustment factors (in addition to the light and temperature factors) should be incorporated into future empirical models of isoprene emissions. Comparison of measured isoprene emissions with estimates of anthropogenic volatile organic compound emissions suggests that isoprene is more important for ozone production in much of Massachusetts on hot summer days when the highest ozone events occur.

  12. Reconciling reported and unreported HFC emissions with atmospheric observations

    PubMed Central

    Lunt, Mark F.; Rigby, Matthew; Ganesan, Anita L.; Manning, Alistair J.; Prinn, Ronald G.; O’Doherty, Simon; Mühle, Jens; Harth, Christina M.; Salameh, Peter K.; Arnold, Tim; Weiss, Ray F.; Saito, Takuya; Yokouchi, Yoko; Krummel, Paul B.; Steele, L. Paul; Fraser, Paul J.; Li, Shanlan; Park, Sunyoung; Reimann, Stefan; Vollmer, Martin K.; Lunder, Chris; Hermansen, Ove; Schmidbauer, Norbert; Maione, Michela; Arduini, Jgor; Young, Dickon; Simmonds, Peter G.

    2015-01-01

    We infer global and regional emissions of five of the most abundant hydrofluorocarbons (HFCs) using atmospheric measurements from the Advanced Global Atmospheric Gases Experiment and the National Institute for Environmental Studies, Japan, networks. We find that the total CO2-equivalent emissions of the five HFCs from countries that are required to provide detailed, annual reports to the United Nations Framework Convention on Climate Change (UNFCCC) increased from 198 (175–221) Tg-CO2-eq⋅y–1 in 2007 to 275 (246–304) Tg-CO2-eq⋅y–1 in 2012. These global warming potential-weighted aggregated emissions agree well with those reported to the UNFCCC throughout this period and indicate that the gap between reported emissions and global HFC emissions derived from atmospheric trends is almost entirely due to emissions from nonreporting countries. However, our measurement-based estimates of individual HFC species suggest that emissions, from reporting countries, of the most abundant HFC, HFC-134a, were only 79% (63–95%) of the UNFCCC inventory total, while other HFC emissions were significantly greater than the reported values. These results suggest that there are inaccuracies in the reporting methods for individual HFCs, which appear to cancel when aggregated together. PMID:25918401

  13. Reconciling reported and unreported HFC emissions with atmospheric observations.

    PubMed

    Lunt, Mark F; Rigby, Matthew; Ganesan, Anita L; Manning, Alistair J; Prinn, Ronald G; O'Doherty, Simon; Mühle, Jens; Harth, Christina M; Salameh, Peter K; Arnold, Tim; Weiss, Ray F; Saito, Takuya; Yokouchi, Yoko; Krummel, Paul B; Steele, L Paul; Fraser, Paul J; Li, Shanlan; Park, Sunyoung; Reimann, Stefan; Vollmer, Martin K; Lunder, Chris; Hermansen, Ove; Schmidbauer, Norbert; Maione, Michela; Arduini, Jgor; Young, Dickon; Simmonds, Peter G

    2015-05-12

    We infer global and regional emissions of five of the most abundant hydrofluorocarbons (HFCs) using atmospheric measurements from the Advanced Global Atmospheric Gases Experiment and the National Institute for Environmental Studies, Japan, networks. We find that the total CO2-equivalent emissions of the five HFCs from countries that are required to provide detailed, annual reports to the United Nations Framework Convention on Climate Change (UNFCCC) increased from 198 (175-221) Tg-CO2-eq ⋅ y(-1) in 2007 to 275 (246-304) Tg-CO2-eq ⋅ y(-1) in 2012. These global warming potential-weighted aggregated emissions agree well with those reported to the UNFCCC throughout this period and indicate that the gap between reported emissions and global HFC emissions derived from atmospheric trends is almost entirely due to emissions from nonreporting countries. However, our measurement-based estimates of individual HFC species suggest that emissions, from reporting countries, of the most abundant HFC, HFC-134a, were only 79% (63-95%) of the UNFCCC inventory total, while other HFC emissions were significantly greater than the reported values. These results suggest that there are inaccuracies in the reporting methods for individual HFCs, which appear to cancel when aggregated together. PMID:25918401

  14. The use of ion chromatography-dc plasma atomic emission spectrometry for the speciation of trace metals. Annual performance report, February 1, 1989--January 31, 1992

    SciTech Connect

    Urasa, I.T.

    1991-09-20

    The original objects of this research program were: to interface d.c. plasma atomic emission spectrometer with an ion chromatograph; to characterize and optimize the combined systems for application in the speciation of metals in aqueous solutions; to use this system in the study of the solution chemistry of various metals; and to find ways in which the measurement sensitivity of the method can be enhanced, thereby allowing the detection of metal species at low ppb concentration levels. This approach has been used to study the chemistry of and speciate several elements in solution including: arsenic, chromium, iron, manganese, nickel phosphorus, platinum, selenium, and vanadium. During the course of this research, we have found that the solution chemistry of the elements studied and the speciation data obtained can vary considerably depending on the solution, and the chromatographic conditions employed. The speciation of chromium, iron, and vanadium was found to be highly influenced by the acidity of the sample. The element selective nature of the d.c. plasma detector allows these changes to be monitored, thereby providing quantitative information on the new moieties formed. New approaches are being developed including the use of chelating ligands as preconcentration agents for purposes of reducing further the detection limits of the elements of interest and to improve the overall element speciation scheme. New thrusts are being directed towards the employment of post-column derivatization method coupled with colorimetric measurements to detect and quantify metal species eluting from the chromatographic column. The influence of sample acidity on these investigations will be carefully evaluated. These new thrusts are described in the accompanying Project Renewal Proposal.

  15. Seasonal NH 3 emissions for the continental united states: Inverse model estimation and evaluation

    NASA Astrophysics Data System (ADS)

    Gilliland, Alice B.; Wyat Appel, K.; Pinder, Robert W.; Dennis, Robin L.

    Significant uncertainty exists in the seasonal distribution of NH 3 emissions since the predominant sources are animal husbandry and fertilizer application. Previous studies that estimated bottom-up and top-down NH 3 emissions have provided the most comprehensive information available about the seasonality of NH 3 emissions. In this study, this bottom-up and top-down emission information is combined with the most recent 2001 USEPA National Emission Inventory (NEI) to construct a best prior estimate of seasonal NH 3 emissions. These emission estimates are then used in an annual 2001 USEPA Community Multiscale Air Quality (CMAQ) model simulation for the continental United States. A key objective of this study is to evaluate these prior NH 3 emission estimates and test the top-down inverse modeling method for a different year and a larger modeling domain than used previously. Based on the final posterior NH 3 emission estimates, the inverse modeling results suggest that the annual total NEI NH 3 emissions are reasonable and that a previous high bias in older USEPA emission inventories has been addressed in the updated inventory. Inverse modeling results suggest that the prior NH 3 emission estimates should be increased in the summer and decreased in the winter, while results for the spring and fall are questionable due to precipitation prediction biases. A final conclusion from this study is that total NH x (NH 3 and aerosol NH 4+) air concentration data are essential for quantitative top-down analyses of NH 3 emissions that can extend beyond what is possible using precipitation chemistry data.

  16. LLNL NESHAPs 1995 annual report

    SciTech Connect

    Gallegos, G.M.; Harrach, R.J.; Biermann, A.H.; Tate, P.J.

    1996-06-01

    This annual report is prepared pursuant to the National Emissions Standards for Hazardous Air Pollutants (NESHAPs) 40 CFR Part 61, Subpart H; Subpart H governs radionuclide emissions to air from Department of Energy (DOE) facilities. NESHAPs limits the emission of radionuclides to the ambient air from DOE facilities to levels resulting in an effective dose equivalent (EDE) of 10 mrem to any member of the public. This document contains the EDEs for the Lawrence Livermore National Laboratory (LLNL) site-wide maximally exposed members of the public from 1995 operations.

  17. Is it Possible to Use the Green Coronal Line Instead of X rays to Cancel an Effect of the Coronal Emissivity Deficit in Estimation of the Prominence Total Mass from Decrease of the EUV-corona Intensities?

    NASA Astrophysics Data System (ADS)

    Schwartz, P.; Heinzel, P.; Jejčič, S.; Rybák, J.; Kotrč, P.; Fárník, F.; Kupryakov, Yu. A.; Deluca, E. E.; Golub, L.; Jibben, P. R.; Anzer, U.; Tlatov, A. G..; Guseva, S. A.

    2016-04-01

    Total masses of six quiescent prominences observed from April through June 2011 were estimated using multi-spectral observations (in EUV, X-rays, Hα, and Ca II H). The method for the total mass estimation is based on the fact that the intensity of the EUV solar corona at wavelengths below 912 Å is reduced at a prominence by the absorption in resonance continua (photoionisation) of hydrogen and possibly by helium and subsequently an amount of absorbed radiation is proportional to the column density of hydrogen and helium plasma. Moreover, the deficit of the coronal emissivity in volume occupied by the cool prominence plasma also contributes to the intensity decrease. The observations in X-rays which are not absorbed by the prominence plasma, allow us to separate these two mechanisms from each other. The X-ray observations of XRT onboard the Hinode satellite made with the Al-mesh focal filter were used because the X-ray coronal radiation formed in plasma of temperatures of the order of 106 K was registered and EUV spectral lines occurring in the 193, 211 and 335 Å channels of the Atmospheric Imaging Assembly of the Solar Dynamics Observatory satellite are also formed at such temperatures. Unfortunately, the Al-mesh filter has a secondary peak of the transmittance at around 171 Å which causes a contribution from the EUV corona to the measured data of up to 11 % in the quiet corona. Thus, absorption in prominence plasma influences XRT X-ray data when using the Al-mesh filter. On the other hand, other X-ray XRT filters are more sensitive to plasma of much higher temperatures (log T of the order of 7), thus observations using these filters cannot be used together with the AIA observations in the method for mass estimations. This problem could be solved using observations in the green coronal line instead of X-rays. Absorption of the green coronal line by a prominence plasma is negligible and this line is formed at temperatures of the order of 106 K. We compare values of the total mass of the prominence observed on 20 October 2012 on the SE limb estimated when using XRT X-ray observations and observations in the green coronal line obtained at Kislovodsk Mountain Astronomical Station of the Pulkovo observatory (Russia).

  18. Particles and gaseous emissions from realistic operation of residential wood pellet heating systems

    NASA Astrophysics Data System (ADS)

    Win, Kaung Myat; Persson, Tomas; Bales, Chris

    2012-11-01

    Gaseous and particulate emissions from six residential wood pellet heating systems are determined at a realistic six day operation sequence. The study aims to investigate the total emissions from a realistic operation of the heating systems including start-up and stop phases. Five combined solar and pellet heating systems and one reference boiler without solar system with an integrated DHW preparation was tested in a laboratory at realistic operation conditions. The investigated emissions comprised carbon monoxide (CO), nitrogen oxide (NO), total organic carbon (TOC) and particulate matter (PM2.5). In this study, the emissions are presented as accumulated total emissions from the whole six days period and the emissions from start-up and stop phases are also presented separately to evaluate the influence of the emissions from these phases on the total emissions. Emission factors of the measured systems from the six day period are between 192 and 547 mg MJ-1 for the CO emissions, between 61 and 95 mg MJ-1 for the NO, between 6 and 45 mg MJ-1 for the TOC, between 31 and 116 mg MJ-1 for the particulate matter and between 2.1 × 1013 and 4 × 1013 for the number of particles. The emissions from the start-up and stop phases are significantly high for the CO (63-95 %) and the TOC (48-93 %). NO and particles emissions are shown to dominate during stationary operation. However, 30-40 % of the particle emissions arise from the start and stop periods. It is also shown that the average emissions of CO, TOC and particles under the realistic annual conditions were higher than the limit values of two eco labels.

  19. Impact of changes in barometric pressure on landfill methane emission

    NASA Astrophysics Data System (ADS)

    Xu, Liukang; Lin, Xiaomao; Amen, Jim; Welding, Karla; McDermitt, Dayle

    2014-07-01

    Landfill methane emissions were measured continuously using the eddy covariance method from June to December 2010. The study site was located at the Bluff Road Landfill in Lincoln, Nebraska, USA. Our results show that landfill methane emissions strongly depended on changes in barometric pressure; rising barometric pressure suppressed the emission, while falling barometric pressure enhanced the emission, a phenomenon called barometric pumping. There was up to a 35-fold variation in day-to-day methane emissions due to changes in barometric pressure. Wavelet coherence analysis revealed a strong spectral coherency between variations of barometric pressure and methane emission at periodicities ranging from 1 day to 8 days. Power spectrum and ogive analysis showed that at least 10 days of continuous measurements was needed in order to capture 90% of the total variance in the methane emission time series at our landfill site. From our results, it is clear that point-in-time measurements taken at monthly or longer time intervals using techniques such as the trace plume method, the mass balance method, or the closed-chamber method will be subject to large variations in measured emission rates because of the barometric pumping phenomenon. Estimates of long-term integrated methane emissions from landfills based on such measurements could yield uncertainties, ranging from 28.8% underestimation to 32.3% overestimation. Our results demonstrate a need for continuous measurements to quantify annual total landfill emissions. This conclusion may apply to the study of methane emissions from wetlands, peatlands, lakes, and other environmental contexts where emissions are from porous media or ebullition. Other implications from the present study for hazard gas monitoring programs are also discussed.

  20. Emission factors for ammonia and nitrous oxide emissions following immediate manure incorporation on two contrasting soil types

    NASA Astrophysics Data System (ADS)

    Webb, J.; Thorman, R. E.; Fernanda-Aller, M.; Jackson, D. R.

    2014-01-01

    We carried out four replicated field experiments to measure the impacts of immediate incorporation of solid manures on emissions of ammonia (NH3) and nitrous oxide (N2O). Four manures: cattle farmyard manure (FYM); pig FYM; layer manure and broiler manure were applied to the soil surface or immediately incorporated by mouldboard plough, disc or tine. Two of the experiments were carried out on a clay soil and two on a sandy soil to find out whether soil type interacted with incorporation technique to influence emissions of NH3 or N2O. Ammonia emissions were measured for 1 or 2 weeks while N2O emissions were measured for 60 days in one experiment and for a complete year in the other three experiments. Immediate incorporation by plough reduced NH3 emissions by c. 90% and by c. 60% by disc and tine (P < 0.001). There was no effect of soil type on NH3 abatement efficiency by plough or tine but the disc was less effective on the coarse sandy soil. Cross-site analysis indicated no effect of incorporation by disc or tine on emissions of N2O-N after 60 days but incorporation by plough increased direct emissions of N2O-N compared with surface application of manure (P < 0.001). Direct emissions of N2O-N, at c. 0.67% of total N applied, were substantially greater at the coarse-textured site than at the heavy clay site (0.04% of total N applied; P < 0.001). The impact of incorporation on total annual direct emissions of N2O-N differed in the three experiments where emissions were measured for a full year. There was no effect of incorporation on N2O-N emissions in the first experiment on the clay soil, and in the second experiment at this site incorporation by plough or disc, but not tine, reduced direct emissions of N2O (P = 0.006). However on the sandy soil direct emissions of N2O-N were increased when manures were incorporated by plough (P = 0.002) but not when incorporated by disc or tine. These results confirm that immediate incorporation of solid manures by plough is the most effective means of reducing NH3 emissions following the application of solid manures. The results also indicate that immediate incorporation of solid manures to reduce NH3 emissions does not necessarily increase emissions of N2O. However, the impacts of immediate incorporation on emissions of N2O may be related to soil type with a greater possibility of emission increases on coarse sandy soils.

  1. (abstract) Determination of the Specific Heat and Total Hemispherical Total Emissivity of the Highly Undercooled Zr(sub 41.2)Ti(sub 13.8)Cu(sub 12.5)Ni(sub 10.0)Be(sub 22.5) Alloy

    NASA Technical Reports Server (NTRS)

    Busch, R.; Kim, Y. J.; Johnson, W. L.; Rulison, A. J.; Rhim, W. K.

    1995-01-01

    High temperature high vacuum electrostatic levitation was combined with DSC experiments to determine the specific heat C(sub p) of the undercooled Zr(sub 41.2)Ti(sub 13.8)Cu(sub 12.5)Ni(sub 10.0)Be(sub 22.5) liquid as a function of temperature. The containerless approach made it possible to undercool the melt to the glass transition temperature without inducing nucleation. Because the cooling process was purely radiative, noncontact temperature measurement techniques could be used to determine the specific heat to total hemispherical emissivity ratio, C(sub p)/epsilon(sub t), for the undercooled liquid region. Using C(sub p) values which were independently obtained by DSC, epsilon(sub t) could be determined. With knowledge of C(sub p) of the undercooled liquid it was possible to determine other thermodynamic properties such as Gibbs free energy and entropy as a function of undercooling.

  2. LLNL NESHAPs 1996 Annual Report

    SciTech Connect

    Gallegos, G.M.

    1997-01-06

    This annual report is prepared pursuant to the National Emissions Standards for Hazardous Air Pollutants (NESHAPs) 40 CFR Part 61, Subpart H; Subpart H governs radionuclide emissions to air from Department of Energy (DOE) facilities. NESHAPs limits the emission of radionuclides to the ambient air from DOE facilities to levels resulting in an annual effective dose equivalent (EDE) of 10 mrem (10 microsieverts) to any member of the public. The EDEs for the Lawrence Livermore National Laboratory (LLNL) site-wide maximally exposed members of the public from 1996 operations were (1) Livermore site: 0. 093 mrem (0.93 microsievert) (52% from point-source emissions, 48% from diffuse-source emissions); (2) Site 300: 0.033 mrem (0.33 microsievert) (99% from point-source, 1% from diffuse-source emissions). The EDEs were generally calculated using the EPA-approved CAP88-PC air-dispersion/dose-assessment model. Site-specific meteorological data, stack flow data, and emissions estimates based on radionuclide inventory data or continuous-monitoring systems data were the specific input to CAP88-PC for each modeled source. 5 figs., 8 tabs.

  3. 40 CFR 89.125 - Production engines, annual report.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 20 2010-07-01 2010-07-01 false Production engines, annual report. 89... (CONTINUED) CONTROL OF EMISSIONS FROM NEW AND IN-USE NONROAD COMPRESSION-IGNITION ENGINES Emission Standards and Certification Provisions § 89.125 Production engines, annual report. (a) Upon the...

  4. 40 CFR 89.125 - Production engines, annual report.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 21 2013-07-01 2013-07-01 false Production engines, annual report. 89... (CONTINUED) CONTROL OF EMISSIONS FROM NEW AND IN-USE NONROAD COMPRESSION-IGNITION ENGINES Emission Standards and Certification Provisions § 89.125 Production engines, annual report. (a) Upon the...

  5. 40 CFR 89.125 - Production engines, annual report.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 20 2014-07-01 2013-07-01 true Production engines, annual report. 89... (CONTINUED) CONTROL OF EMISSIONS FROM NEW AND IN-USE NONROAD COMPRESSION-IGNITION ENGINES Emission Standards and Certification Provisions § 89.125 Production engines, annual report. (a) Upon the...

  6. 40 CFR 89.125 - Production engines, annual report.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 21 2012-07-01 2012-07-01 false Production engines, annual report. 89... (CONTINUED) CONTROL OF EMISSIONS FROM NEW AND IN-USE NONROAD COMPRESSION-IGNITION ENGINES Emission Standards and Certification Provisions § 89.125 Production engines, annual report. (a) Upon the...

  7. 40 CFR 89.125 - Production engines, annual report.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 20 2011-07-01 2011-07-01 false Production engines, annual report. 89... (CONTINUED) CONTROL OF EMISSIONS FROM NEW AND IN-USE NONROAD COMPRESSION-IGNITION ENGINES Emission Standards and Certification Provisions § 89.125 Production engines, annual report. (a) Upon the...

  8. The socioeconomic drivers of Chinas primary PM2.5 emissions

    NASA Astrophysics Data System (ADS)

    Guan, Dabo; Su, Xin; Zhang, Qiang; Peters, Glen P.; Liu, Zhu; Lei, Yu; He, Kebin

    2014-01-01

    Primary PM2.5 emissions contributed significantly to poor air quality in China. We present an interdisciplinary study to measure the magnitudes of socioeconomic factors in driving primary PM2.5 emission changes in China between 1997-2010, by using a regional emission inventory as input into an environmentally extended input-output framework and applying structural decomposition analysis. Our results show that Chinas significant efficiency gains fully offset emissions growth triggered by economic growth and other drivers. Capital formation is the largest final demand category in contributing annual PM2.5 emissions, but the associated emission level is steadily declining. Exports is the only final demand category that drives emission growth between 1997-2010. The production of exports led to emissions of 638 thousand tonnes of PM2.5, half of the EU27 annual total, and six times that of Germany. Embodied emissions in Chinese exports are largely driven by consumption in OECD countries.

  9. A UK inventory of nitrous oxide emissions from farmed livestock

    NASA Astrophysics Data System (ADS)

    Chadwick, D. R.; Sneath, R. W.; Phillips, V. R.; Pain, B. F.

    A UK inventory of the nitrous oxide (N 2O) emissions from farmed livestock was compiled to identify areas where potential abatement practices may be effective. Where possible, emission factors based on direct experimental data gathered under UK conditions were used, but published data were used when this was not feasible, together with statistical information, which included details of numbers of animals within each category of a species, animal liveweights, number of days housed, excretal rates and volumes of manures in stores. Total N 2O emissions were calculated for each component of livestock production systems, i.e. animal houses, manure stores, following application of manures to land and during grazing. Emissions were also estimated from land used for forage conservation and tillage. Total annual N 2O emissions from UK farmed livestock, based mainly on 1996 animal census data, were estimated to be 38.27 kt. The two main terms were 22.66 kt N 2O from mineral fertilisers after application to soils and 5.61 kt N 2O from stored manures (mainly in the form of farmyard manure). Within buildings, poultry were the largest contributors of N 2O, 2.97 kt, followed by cattle, 1.62 kt. Within the total emissions from stored manures, cattle were the largest contributors of N 2O, 3.58 kt, followed by poultry, 1.86 kt. Dietary manipulation and a move from solid manure based systems to slurry based systems appear to be promising abatement practices.

  10. The contribution of evaporative emissions from gasoline vehicles to the volatile organic compound inventory in Mexico City.

    PubMed

    Schifter, I; Díaz, L; Rodríguez, R; González-Macías, C

    2014-06-01

    The strategy for decreasing volatile organic compound emissions in Mexico has been focused much more on tailpipe emissions than on evaporative emissions, so there is very little information on the contribution of evaporative emissions to the total volatile organic compound inventory. We examined the magnitudes of exhaust and evaporative volatile organic compound emissions, and the species emitted, in a representative fleet of light-duty gasoline vehicles in the Metropolitan Area of Mexico City. The US "FTP-75" test protocol was used to estimate volatile organic compound emissions associated with diurnal evaporative losses, and when the engine is started and a journey begins. The amount and nature of the volatile organic compounds emitted under these conditions have not previously been accounted in the official inventory of the area. Evaporative emissions from light-duty vehicles in the Metropolitan Area of Mexico City were estimated to be 39 % of the total annual amount of hydrocarbons emitted. Vehicles built before 1992 (16 % of the fleet) were found to be responsible for 43 % of the total hydrocarbon emissions from exhausts and 31 % of the evaporative emissions of organic compounds. The relatively high amounts of volatile organic compounds emitted from older vehicles found in this study show that strong emission controls need to be implemented in order to decrease the contribution of evaporative emissions of this fraction of the fleet. PMID:24526614

  11. Hypergolic oxidizer and fuel scrubber emissions

    NASA Technical Reports Server (NTRS)

    Parrish, Clyde F.; Barile, Ronald G.; Curran, Dan; Hodge, Tim; Lueck, Dale E.; Young, Rebecca C.

    1995-01-01

    Hypergolic fuels and oxidizer are emitted to the environment during fueling and deservicing shuttle and other spacecraft. Such emissions are difficult to measure due to the intermittent purge flow and to the presence of suspended scrubber liquor. A new method for emissions monitoring was introduced in a previous paper. This paper is a summary of the results of a one-year study of shuttle launch pads and orbiter processing facilities (OPF's) which proved that emissions can be determined from field scrubbers without direct measurement of vent flow rate and hypergol concentration. This new approach is based on the scrubber efficiency, which was measured during normal operations, and on the accumulated weight of hypergol captured in the scrubber liquor, which is part of the routine monitoring data of scrubber liquors. To validate this concept, three qualification tests were performed, logs were prepared for each of 16 hypergol scrubbers at KSC, the efficiencies of KSC scrubbers were measured during normal operations, and an estimate of the annual emissions was made based on the efficiencies and the propellant buildup data. The results have confirmed that the emissions from the KSC scrubbers can be monitored by measuring the buildup of hypergol propellant in the liquor, and then using the appropriate efficiency to calculate the emissions. There was good agreement between the calculated emissions based on outlet concentration and flow rate, and the emissions calculated from the propellant buildup and efficiency. The efficiencies of 12 KSC scrubbers, measured under actual servicing operations and special test conditions, were assumed to be valid for all subsequent operations until a significant change in hardware occurred. An estimate of the total emissions from 16 scrubbers for three years showed that 0.3 kg/yr of fuel and 234 kg/yr of oxidizer were emitted.

  12. Mercury emissions from municipal solid waste combustors

    SciTech Connect

    Not Available

    1993-05-01

    This report examines emissions of mercury (Hg) from municipal solid waste (MSW) combustion in the United States (US). It is projected that total annual nationwide MSW combustor emissions of mercury could decrease from about 97 tonnes (1989 baseline uncontrolled emissions) to less than about 4 tonnes in the year 2000. This represents approximately a 95 percent reduction in the amount of mercury emitted from combusted MSW compared to the 1989 mercury emissions baseline. The likelihood that routinely achievable mercury emissions removal efficiencies of about 80 percent or more can be assured; it is estimated that MSW combustors in the US could prove to be a comparatively minor source of mercury emissions after about 1995. This forecast assumes that diligent measures to control mercury emissions, such as via use of supplemental control technologies (e.g., carbon adsorption), are generally employed at that time. However, no present consensus was found that such emissions control measures can be implemented industry-wide in the US within this time frame. Although the availability of technology is apparently not a limiting factor, practical implementation of necessary control technology may be limited by administrative constraints and other considerations (e.g., planning, budgeting, regulatory compliance requirements, etc.). These projections assume that: (a) about 80 percent mercury emissions reduction control efficiency is achieved with air pollution control equipment likely to be employed by that time; (b) most cylinder-shaped mercury-zinc (CSMZ) batteries used in hospital applications can be prevented from being disposed into the MSW stream or are replaced with alternative batteries that do not contain mercury; and (c) either the amount of mercury used in fluorescent lamps is decreased to an industry-wide average of about 27 milligrams of mercury per lamp or extensive diversion from the MSW stream of fluorescent lamps that contain mercury is accomplished.

  13. The effects of energy paths and emission controls and standards on future trends in China's emissions of primary air pollutants

    NASA Astrophysics Data System (ADS)

    Zhao, Y.; Zhang, J.; Nielsen, C. P.

    2014-03-01

    To examine the efficacy of China's actions to control atmospheric pollution, three levels of growth of energy consumption and three levels of implementation of emission controls are estimated, generating a total of nine combined activity-emission control scenarios that are then used to estimate trends of national emissions of primary air pollutants through 2030. The emission control strategies are expected to have more effects than the energy paths on the future emission trends for all the concerned pollutants. As recently promulgated national action plans of air pollution prevention and control (NAPAPPC) are implemented, China's anthropogenic pollutant emissions should decline. For example, the emissions of SO2, NOx, total primary particulate matter (PM), PM10, and PM2.5 are estimated to decline 7%, 20%, 41%, 34%, and 31% from 2010 to 2030, respectively, in the "best guess" scenario that includes national commitment of energy saving policy and partial implementation of NAPAPPC. Should the issued/proposed emission standards be fully achieved, a less likely scenario, annual emissions would be further reduced, ranging from 17% (for primary PM2.5) to 29% (for NOx) declines in 2015, and the analogue numbers would be 12% and 24% in 2030. The uncertainties of emission projections result mainly from the uncertain operational conditions of swiftly proliferating air pollutant control devices and lack of detailed information about emission control plans by region. The predicted emission trends by sector and chemical species raise concerns about current pollution control strategies: the potential for emissions abatement in key sectors may be declining due to the near saturation of emission control devices use; risks of ecosystem acidification could rise because emissions of alkaline base cations may be declining faster than those of SO2; and radiative forcing could rise because emissions of positive-forcing carbonaceous aerosols may decline more slowly than those of SO2 emissions and thereby concentrations of negative-forcing sulfate particles. Expanded control of emissions of fine particles and carbonaceous aerosols from small industrial and residential sources is recommended, and a more comprehensive emission control strategy targeting a wider range of pollutants and taking account of more diverse environmental impacts is also urgently needed.

  14. The effects of energy paths and emission controls and standards on future trends in China's emissions of primary air pollutants

    NASA Astrophysics Data System (ADS)

    Zhao, Y.; Zhang, J.; Nielsen, C. P.

    2014-09-01

    To examine the efficacy of China's actions to control atmospheric pollution, three levels of growth of energy consumption and three levels of implementation of emission controls are estimated, generating a total of nine combined activity-emission control scenarios that are then used to estimate trends of national emissions of primary air pollutants through 2030. The emission control strategies are expected to have more effects than the energy paths on the future emission trends for all the concerned pollutants. As recently promulgated national action plans of air pollution prevention and control (NAPAPPC) are implemented, China's anthropogenic pollutant emissions should decline. For example, the emissions of SO2, NOx, total suspended particles (TSP), PM10, and PM2.5 are estimated to decline 7, 20, 41, 34, and 31% from 2010 to 2030, respectively, in the "best guess" scenario that includes national commitment of energy saving policy and implementation of NAPAPPC. Should the issued/proposed emission standards be fully achieved, a less likely scenario, annual emissions would be further reduced, ranging from 17 (for primary PM2.5) to 29% (for NOx) declines in 2015, and the analogue numbers would be 12 and 24% in 2030. The uncertainties of emission projections result mainly from the uncertain operational conditions of swiftly proliferating air pollutant control devices and lack of detailed information about emission control plans by region. The predicted emission trends by sector and chemical species raise concerns about current pollution control strategies: the potential for emissions abatement in key sectors may be declining due to the near saturation of emission control devices use; risks of ecosystem acidification could rise because emissions of alkaline base cations may be declining faster than those of SO2; and radiative forcing could rise because emissions of positive-forcing carbonaceous aerosols may decline more slowly than those of SO2 emissions and thereby concentrations of negative-forcing sulfate particles. Expanded control of emissions of fine particles and carbonaceous aerosols from small industrial and residential sources is recommended, and a more comprehensive emission control strategy targeting a wider range of pollutants (volatile organic compounds, NH3 and CO, etc.) and taking account of more diverse environmental impacts is also urgently needed.

  15. Lower Monoamine Oxidase-A Total Distribution Volume in Impulsive and Violent Male Offenders with Antisocial Personality Disorder and High Psychopathic Traits: An [(11)C] Harmine Positron Emission Tomography Study.

    PubMed

    Kolla, Nathan J; Matthews, Brittany; Wilson, Alan A; Houle, Sylvain; Bagby, R Michael; Links, Paul; Simpson, Alexander I; Hussain, Amina; Meyer, Jeffrey H

    2015-10-01

    Antisocial personality disorder (ASPD) often presents with highly impulsive, violent behavior, and pathological changes in the orbitofrontal cortex (OFC) and ventral striatum (VS) are implicated. Several compelling reasons support a relationship between low monoamine oxidase-A (MAO-A), an enzyme that regulates neurotransmitters, and ASPD. These include MAO-A knockout models in rodents evidencing impulsive aggression and positron emission tomography (PET) studies of healthy subjects reporting associations between low brain MAO-A levels and greater impulsivity or aggression. However, a fundamental gap in the literature is that it is unknown whether brain MAO-A levels are low in more severe, clinical disorders of impulsivity, such as ASPD. To address this issue, we applied [(11)C] harmine PET to measure MAO-A total distribution volume (MAO-A VT), an index of MAO-A density, in 18 male ASPD participants and 18 age- and sex-matched controls. OFC and VS MAO-A VT were lower in ASPD compared with controls (multivariate analysis of variance (MANOVA): F2,33=6.8, P=0.003; OFC and VS MAO-A VT each lower by 19%). Similar effects were observed in other brain regions: prefrontal cortex, anterior cingulate cortex, dorsal putamen, thalamus, hippocampus, and midbrain (MANOVA: F7,28=2.7, P=0.029). In ASPD, VS MAO-A VT was consistently negatively correlated with self-report and behavioral measures of impulsivity (r=-0.50 to -0.52, all P-values<0.05). This study is the first to demonstrate lower brain MAO-A levels in ASPD. Our results support an important extension of preclinical models of impulsive aggression into a human disorder marked by pathological aggression and impulsivity. PMID:26081301

  16. Detection of Long-Term Change in Methane Emissions Using Atmospheric Network Observations

    NASA Astrophysics Data System (ADS)

    Bruhwiler, L.

    2014-12-01

    The number of sites in the Arctic at which observations of atmospheric CH4 are collected has grown over the past several decades. Some of these sites now have observation records that span several decades; from the early 1980s to present. At the same time, Arctic temperatures have increased at double the rate of the global average increase. A recent comparison of models of CH4 emissions from wetlands (the "WETCHIMP" study) found that many models predict increased emissions in response to higher temperatures. Given the temperature sensitivity of the wetland emission models, and the observed Arctic temperature increase, the change in annual CH4 emissions is likely small, however, the cumulative extra emissions over this period may be at the detection level of the atmospheric network. Even so there is still no firm evidence from the atmospheric network that emissions are changing. In this study, we explore the sensitivity of the atmospheric network to changing emissions. How large do the emissions have to be before they can be seen in the network observations? Can changes be detected by using spatial gradients of observed methane? Can changes in the amplitude and phase of the annual cycle be used to detect increasing emissions during the growing season? Furthermore, by using atmospheric assimilation techniques, network observations provide a strong constraint on total Arctic emissions. Using results from a suite of atmospheric CH4 assimilations we show that total emissions from the Arctic are ~25 TgCH4/yr (with a range from 18 to 29 TgCH4/yr). This is lower than many bottom-up analyses, and implies that emissions from Arctic lakes, the Eastern Siberian Arctic Sea, wetlands and possible geologic sources cannot all be accommodated in the Arctic atmospheric budget of CH4. Finally, we address the issue of how the observation network can be augmented to allow timely trend detection.

  17. Methane emission from natural wetlands: Global distribution, area, and environmental characteristics of sources

    SciTech Connect

    Matthews, E.; Fung, I. )

    1987-03-01

    A global data base of wetlands at 1 degree resolution was developed from the integration of three independent global, digital sources: (1) vegetation, (2) soil properties and (3) fractional inundation in each 1 degree cell. The integration yielded a global distribution of wetland sites identified with in situ ecological and environmental characteristics. The wetland sites were classified into five major groups on the basis of environmental characteristics governing methane emissions. The global wetland area derived in this study is 5.3 trillion sq m, approximately twice the wetland area previously used in methane emission studies. Methane emission was calculated using methane fluxes for the major wetland groups, and simple assumptions about the duration of the methane production season. The annual methane emission from wetlands is about 110 Tg, well within the range of previous estimates. Tropical/subtropical peat-poor swamps from 20 degrees N to 30 degrees S account from 30% of the global wetland area and 25% of the total methane emission. About 60% of the total emission comes from peat-rich bogs concentrated from 50-70 degrees N, suggesting that the highly seasonal emission from these ecosystems is the major contributor to the large annual oscillations observed in atmospheric methane concentrations at these latitudes. 78 refs., 6 figs., 5 tabs.

  18. Cold season emissions dominate the Arctic tundra methane budget.

    PubMed

    Zona, Donatella; Gioli, Beniamino; Commane, Róisín; Lindaas, Jakob; Wofsy, Steven C; Miller, Charles E; Dinardo, Steven J; Dengel, Sigrid; Sweeney, Colm; Karion, Anna; Chang, Rachel Y-W; Henderson, John M; Murphy, Patrick C; Goodrich, Jordan P; Moreaux, Virginie; Liljedahl, Anna; Watts, Jennifer D; Kimball, John S; Lipson, David A; Oechel, Walter C

    2016-01-01

    Arctic terrestrial ecosystems are major global sources of methane (CH4); hence, it is important to understand the seasonal and climatic controls on CH4 emissions from these systems. Here, we report year-round CH4 emissions from Alaskan Arctic tundra eddy flux sites and regional fluxes derived from aircraft data. We find that emissions during the cold season (September to May) account for ≥ 50% of the annual CH4 flux, with the highest emissions from noninundated upland tundra. A major fraction of cold season emissions occur during the "zero curtain" period, when subsurface soil temperatures are poised near 0 °C. The zero curtain may persist longer than the growing season, and CH4 emissions are enhanced when the duration is extended by a deep thawed layer as can occur with thick snow cover. Regional scale fluxes of CH4 derived from aircraft data demonstrate the large spatial extent of late season CH4 emissions. Scaled to the circumpolar Arctic, cold season fluxes from tundra total 12 ± 5 (95% confidence interval) Tg CH4 y(-1), ∼ 25% of global emissions from extratropical wetlands, or ∼ 6% of total global wetland methane emissions. The dominance of late-season emissions, sensitivity to soil environmental conditions, and importance of dry tundra are not currently simulated in most global climate models. Because Arctic warming disproportionally impacts the cold season, our results suggest that higher cold-season CH4 emissions will result from observed and predicted increases in snow thickness, active layer depth, and soil temperature, representing important positive feedbacks on climate warming. PMID:26699476

  19. Cold season emissions dominate the Arctic tundra methane budget

    PubMed Central

    Zona, Donatella; Gioli, Beniamino; Lindaas, Jakob; Wofsy, Steven C.; Miller, Charles E.; Dinardo, Steven J.; Dengel, Sigrid; Sweeney, Colm; Karion, Anna; Chang, Rachel Y.-W.; Henderson, John M.; Murphy, Patrick C.; Goodrich, Jordan P.; Moreaux, Virginie; Liljedahl, Anna; Watts, Jennifer D.; Kimball, John S.; Lipson, David A.; Oechel, Walter C.

    2016-01-01

    Arctic terrestrial ecosystems are major global sources of methane (CH4); hence, it is important to understand the seasonal and climatic controls on CH4 emissions from these systems. Here, we report year-round CH4 emissions from Alaskan Arctic tundra eddy flux sites and regional fluxes derived from aircraft data. We find that emissions during the cold season (September to May) account for ≥50% of the annual CH4 flux, with the highest emissions from noninundated upland tundra. A major fraction of cold season emissions occur during the “zero curtain” period, when subsurface soil temperatures are poised near 0 °C. The zero curtain may persist longer than the growing season, and CH4 emissions are enhanced when the duration is extended by a deep thawed layer as can occur with thick snow cover. Regional scale fluxes of CH4 derived from aircraft data demonstrate the large spatial extent of late season CH4 emissions. Scaled to the circumpolar Arctic, cold season fluxes from tundra total 12 ± 5 (95% confidence interval) Tg CH4 y−1, ∼25% of global emissions from extratropical wetlands, or ∼6% of total global wetland methane emissions. The dominance of late-season emissions, sensitivity to soil environmental conditions, and importance of dry tundra are not currently simulated in most global climate models. Because Arctic warming disproportionally impacts the cold season, our results suggest that higher cold-season CH4 emissions will result from observed and predicted increases in snow thickness, active layer depth, and soil temperature, representing important positive feedbacks on climate warming. PMID:26699476

  20. Carbon dioxide emissions from an Acacia plantation on peatland in Sumatra, Indonesia

    NASA Astrophysics Data System (ADS)

    Jauhiainen, J.; Hooijer, A.; Page, S. E.

    2012-02-01

    Peat surface CO2 emission, groundwater table depth and peat temperature were monitored for two years along transects in an Acacia plantation on thick tropical peat (>4 m) in Sumatra, Indonesia. A total of 2300 emission measurements were taken at 144 locations, over a 2 year period. The autotrophic root respiration component of CO2 emission was separated from heterotrophic emission caused by peat oxidation in three ways: (i) by comparing CO2 emissions within and beyond the tree rooting zone, (ii) by comparing CO2 emissions with and without peat trenching (i.e. cutting any roots remaining in the peat beyond the tree rooting zone), and (iii) by comparing CO2 emissions before and after Acacia tree harvesting. On average, the contribution of autotrophic respiration to daytime CO2 emission was 21% along transects in mature tree stands. At locations 0.5 m from trees this was up to 80% of the total emissions, but it was negligible at locations more than 1.3 m away. This means that CO2 emission measurements well away from trees were free of any autotrophic respiration contribution and thus represent only heterotrophic emissions. We found daytime mean annual CO2 emission from peat oxidation alone of 94 t ha-1 y-1 at a mean water table depth of 0.8 m, and a minimum emission value of 80 t ha-1 y-1 after correction for the effect of diurnal temperature fluctuations, which may result in a 14.5% reduction of the daytime emission. There is a positive correlation between mean long-term water table depth and peat oxidation CO2 emission. However, no such relation is found for instantaneous emission/water table depth within transects and it is clear that factors other than water table depth also affect peat oxidation and total CO2 emissions. The increase in the temperature of the surface peat due to plantation establishment may explain over 50% of peat oxidation emissions. Our study sets a standard for greenhouse gas flux studies from tropical peatlands under different forms of agricultural land management. It is the first to purposefully quantify heterotrophic CO2 emissions resulting from tropical peat decomposition by separating these from autotrophic emissions. It also provides the most scientifically- and statistically-rigorous study to date of CO2 emissions resulting from anthropogenic modification of this globally significant carbon rich ecosystem. Our findings indicate that past studies have underestimated emissions from peatland plantations, with important implications for the scale of greenhouse gas emissions arising from land use change, particularly in the light of current, rapid agricultural conversion of peatlands in the Southeast Asian region.

  1. Coal industry annual 1997

    SciTech Connect

    1998-12-01

    Coal Industry Annual 1997 provides comprehensive information about US coal production, number of mines, prices, productivity, employment, productive capacity, and recoverable reserves. US Coal production for 1997 and previous years is based on the annual survey EIA-7A, Coal Production Report. This report presents data on coal consumption, coal distribution, coal stocks, coal prices, and coal quality for Congress, Federal and State agencies, the coal industry, and the general public. Appendix A contains a compilation of coal statistics for the major coal-producing States. This report includes a national total coal consumption for nonutility power producers that are not in the manufacturing, agriculture, mining, construction, or commercial sectors. 14 figs., 145 tabs.

  2. Annual Energy Review 2007

    SciTech Connect

    Seiferlein, Katherine E.

    2008-06-01

    The Annual Energy Review (AER) is the Energy Information Administration's (EIA) primary report of annual historical energy statistics. For many series, data begin with the year 1949. Included are data on total energy production, consumption, and trade; overviews of petroleum, natural gas, coal, electricity, nuclear energy, renewable energy, international energy, as well as financial and environment indicators; and data unit conversion tables. Publication of this report is required under Public Law 95–91 (Department of Energy Organization Act), Section 205(c), and is in keeping with responsibilities given to the EIA under Section 205(a)(2), which states: “The Administrator shall be responsible for carrying out a central, comprehensive, and unified energy data and information program which will collect, evaluate, assemble, analyze, and disseminate data and information....”

  3. Biomass Burning Emissions and Deforestation in The Legal Amazon

    NASA Astrophysics Data System (ADS)

    Ellicott, E. A.; Vermote, E. F.

    2010-12-01

    Biomass burning, often concomitant with deforestation, is recognized as a significant source of atmospheric trace gases and aerosols and has received attention from the scientific community as an important agent in climate change. Earth observing satellites have made significant contributions to fire and deforestation detection, monitoring, and characterization for nearly three decades. In this work, we demonstrate the application of our approach to estimate fire radiative energy (FRE) released from biomass burning to infer CO2 and organic and black carbon aerosol (OCBC) emissions from biomass burning in the Legal Amazon. We then compared emission estimates with deforestation rates produced by the Brazilian National Institute for Space Research (INPE). Our research offers a new approach and insights to the dynamics of fire, deforestation, emissions. The annual mean CO2 and OCBC emitted for the study period (2001-2009) from the Legal Amazon biomass burning was estimated to be 253 Tg and 2.3 Tg, respectively. This represents 9% and 14% of the global CO2 and OCBC, respectively, emitted from fires. In general, the trend in emission estimates mirrored deforestation rates. However, 2007 was an anomalous year in Brazil as it was one of the highest years in emissions from fire, but a relatively low year for deforestation (Fig. 1). This discrepancy is a result of an abnormally dry year which resulted in a greater frequency of fires not directly associated with deforestation, but which may be tied to agricultural and pasture maintenance fires. A similar discrepancy was observed when comparing deforestation and emission rates from Mato Grosso and Pará; the two states responsible for most of the deforestation (71%) and emissions (~65%) from the Legal Amazon during the study period. Although as of 2006 Pará had annually surpassed Mato Grosso in annual forest loss it wasn’t until 2009 that emissions from Pará were greater. Thus, suggesting the importance of non-deforestation related fires to total annual emissions in Mato Grosso. Therefore, any discussion of reducing emissions from deforestation and degradation (REDD+) should also consider the implications of fire as a tool for managing the land after deforestation has occurred.

  4. Impact of Biogenic Emission Uncertainties on the Simulated Response of Ozone and Fine Particulate Matter to Anthropogenic Emission Reductions

    PubMed Central

    Hogrefe, Christian; Isukapalli, Sastry S.; Tang, Xiaogang; Georgopoulos, Panos G.; He, Shan; Zalewsky, Eric E.; Hao, Winston; Ku, Jia-Yeong; Key, Tonalee; Sistla, Gopal

    2011-01-01

    The role of emissions of volatile organic compounds and nitric oxide from biogenic sources is becoming increasingly important in regulatory air quality modeling as levels of anthropogenic emissions continue to decrease and stricter health-based air quality standards are being adopted. However, considerable uncertainties still exist in the current estimation methodologies for biogenic emissions. The impact of these uncertainties on ozone and fine particulate matter (PM2.5) levels for the eastern United States was studied, focusing on biogenic emissions estimates from two commonly used biogenic emission models, the Model of Emissions of Gases and Aerosols from Nature (MEGAN) and the Biogenic Emissions Inventory System (BEIS). Photochemical grid modeling simulations were performed for two scenarios: one reflecting present day conditions and the other reflecting a hypothetical future year with reductions in emissions of anthropogenic oxides of nitrogen (NOx). For ozone, the use of MEGAN emissions resulted in a higher ozone response to hypothetical anthropogenic NOx emission reductions compared with BEIS. Applying the current U.S. Environmental Protection Agency guidance on regulatory air quality modeling in conjunction with typical maximum ozone concentrations, the differences in estimated future year ozone design values (DVF) stemming from differences in biogenic emissions estimates were on the order of 4 parts per billion (ppb), corresponding to approximately 5% of the daily maximum 8-hr ozone National Ambient Air Quality Standard (NAAQS) of 75 ppb. For PM2.5, the differences were 0.1–0.25 μg/m3 in the summer total organic mass component of DVFs, corresponding to approximately 1–2% of the value of the annual PM2.5 NAAQS of 15 μg/m3. Spatial variations in the ozone and PM2.5 differences also reveal that the impacts of different biogenic emission estimates on ozone and PM2.5 levels are dependent on ambient levels of anthropogenic emissions. PMID:21305893

  5. 40 CFR 61.162 - Emission limits.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS National Emission Standard for Inorganic Arsenic Emissions... total arsenic emissions from the glass melting furnace shall be less than 2.5 Mg (2.7 ton) per year, or (2) Total arsenic emissions from the glass melting furnace shall be conveyed to a control device...

  6. 40 CFR 61.162 - Emission limits.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS National Emission Standard for Inorganic Arsenic Emissions... total arsenic emissions from the glass melting furnace shall be less than 2.5 Mg (2.7 ton) per year, or (2) Total arsenic emissions from the glass melting furnace shall be conveyed to a control device...

  7. The contribution of soil biogenic NO emissions from a managed hyper-arid ecosystem to the regional NO2 emissions during growing season

    NASA Astrophysics Data System (ADS)

    Mamtimin, B.; Badawy, M.; Behrendt, T.; Meixner, F. X.; Wagner, T.

    2015-12-01

    A study was carried out to understand the contributions of soil biogenic NO emissions from managed (fertilized and irrigated) hyper-arid ecosystem in NW-China to the regional NO2 emissions during growing season. Soil biogenic NO emissions were quantified by laboratory incubation of corresponding soil samples. We have developed the Geoscience General Tool Package (GGTP) to obtain soil temperature, soil moisture and biogenic soil NO emission at oasis scale. Bottom-up anthropogenic NO2 emissions have been scaled down from annual to monthly values to compare mean monthly soil biogenic NO2 emissions. The top-down emission estimates have been derived from satellite observations compared then with the bottom-up emission estimates (anthropogenic and biogenic). The results show that the soil biogenic emissions of NO2 during the growing period are (at least) equal until twofold of the related anthropogenic sources. We found that the grape soils are the main summertime contributor to the biogenic NO emissions of study area, followed by cotton soils. The top-down and bottom-up emission estimates were shown to be useful methods to estimate the monthly/seasonal cycle of the total regional NO2 emissions. The resulting total NO2 emissions show a strong peak in winter and a secondary peak in summer, providing confidence in the method. These findings provide strong evidence that biogenic emissions from soils of managed drylands (irrigated and fertilized) in the growing period can be much more important contributors to the regional NO2 budget (hence to regional photochemistry) of dryland regions than thought before.

  8. Methane Emissions from United States Natural Gas Gathering and Processing.

    PubMed

    Marchese, Anthony J; Vaughn, Timothy L; Zimmerle, Daniel J; Martinez, David M; Williams, Laurie L; Robinson, Allen L; Mitchell, Austin L; Subramanian, R; Tkacik, Daniel S; Roscioli, Joseph R; Herndon, Scott C

    2015-09-01

    New facility-level methane (CH4) emissions measurements obtained from 114 natural gas gathering facilities and 16 processing plants in 13 U.S. states were combined with facility counts obtained from state and national databases in a Monte Carlo simulation to estimate CH4 emissions from U.S. natural gas gathering and processing operations. Total annual CH4 emissions of 2421 (+245/-237) Gg were estimated for all U.S. gathering and processing operations, which represents a CH4 loss rate of 0.47% (±0.05%) when normalized by 2012 CH4 production. Over 90% of those emissions were attributed to normal operation of gathering facilities (1697 +189/-185 Gg) and processing plants (506 +55/-52 Gg), with the balance attributed to gathering pipelines and processing plant routine maintenance and upsets. The median CH4 emissions estimate for processing plants is a factor of 1.7 lower than the 2012 EPA Greenhouse Gas Inventory (GHGI) estimate, with the difference due largely to fewer reciprocating compressors, and a factor of 3.0 higher than that reported under the EPA Greenhouse Gas Reporting Program. Since gathering operations are currently embedded within the production segment of the EPA GHGI, direct comparison to our results is complicated. However, the study results suggest that CH4 emissions from gathering are substantially higher than the current EPA GHGI estimate and are equivalent to 30% of the total net CH4 emissions in the natural gas systems GHGI. Because CH4 emissions from most gathering facilities are not reported under the current rule and not all source categories are reported for processing plants, the total CH4 emissions from gathering and processing reported under the EPA GHGRP (180 Gg) represents only 14% of that tabulated in the EPA GHGI and 7% of that predicted from this study. PMID:26281719

  9. Factors affecting methane emission from rice fields

    NASA Astrophysics Data System (ADS)

    Neue, H. U.; Wassmann, R.; Lantin, R. S.; Alberto, Ma C. R.; Aduna, J. B.; Javellana, A. M.

    Emission of CH 4 from ricefields is the result of anoxic bacterial methane production. Global estimates of annual CH 4 emission from ricefields is 100 Tg. CH 4 emission data from limited sites are tentative. It is essential that uncertainty in individual sources is reduced in order to develop feasible and effective mitigation options which do not negate gains in rice production and productivity. Field studies at the International Rice Research Institute show that soil and added organic matter are the sources for initial methane production. Addition of rice straw enhances methane production. Roots and root exudates of wetland rice plants appear to be the major carbon sources at ripening stage. The production and transport of CH 4 to the atmosphere depend on properties of the rice plant. Under the same spacing and fertilization, the traditional variety Dular emitted more CH 4 per day than did the new plant type IR65597. Upon flooding for land preparation anaerobic conditions result in significant amount of methane being formed. Drying the field at midtillering significantly reduced total CH 4 emissions. Large amounts of entrapped CH 4 escape to the atmosphere when floodwater recedes upon drying at harvest. Cultural practices may account for 20% of the overall seasonal CH 4 emissions.

  10. Compilation and application of Japanese inventories for energy consumption and air pollutant emissions using input-output tables.

    PubMed

    Nansai, Keisuke; Moriguchi, Yuichi; Tohno, Susumu

    2003-05-01

    Preparing emission inventories is essential to the assessment and management of our environment. In this study, Japanese air pollutant emissions, energy consumption, and CO2 emissions categorized by approximately 400 sectors (as classified by Japanese input-output tables in 1995) were estimated, and the contributions of each sector to the total amounts were analyzed. The air pollutants examined were nitrogen oxides (NOx), sulfur oxides (SOx), and suspended particulate matter (SPM). Consumptions of about 20 fossil fuels and five other fuels were estimated according to sector. Air pollutant emission factors for stationary sources were calculated from the results of a survey on air pollution prevention in Japan. Pollutant emissions from mobile sources were estimated taking into consideration vehicle types, traveling speeds, and distances. This work also counted energy supply and emissions from seven nonfossil fuel sources, including nonthermal electric power, and CO2 emissions from limestone (for example, during cement production). The total energy consumption in 1995 was concluded to be 18.3 EJ, and the annual total emissions of CO2, NOx, SOx, and SPM were, respectively, 343 Mt-C, 3.51 Mt, 1.87 Mt, and 0.32 Mt. An input-output analysis of the emission inventories was used to calculate the amounts of energy consumption and emissions induced in each sector by the economic final demand. PMID:12775078

  11. Comparison of road traffic emission models in Madrid (Spain)

    NASA Astrophysics Data System (ADS)

    Borge, Rafael; de Miguel, Isabel; de la Paz, David; Lumbreras, Julio; Pérez, Javier; Rodríguez, Encarnación

    2012-12-01

    Many cities in Europe have difficulties to meet the air quality standards set by the European legislation, most particularly the annual mean Limit Value for NO2. Road transport is often the main source of air pollution in urban areas and therefore, there is an increasing need to estimate current and future traffic emissions as accurately as possible. As a consequence, a number of specific emission models and emission factors databases have been developed recently. They present important methodological differences and may result in largely diverging emission figures and thus may lead to alternative policy recommendations. This study compares two approaches to estimate road traffic emissions in Madrid (Spain): the COmputer Programme to calculate Emissions from Road Transport (COPERT4 v.8.1) and the Handbook Emission Factors for Road Transport (HBEFA v.3.1), representative of the 'average-speed' and 'traffic situation' model types respectively. The input information (e.g. fleet composition, vehicle kilometres travelled, traffic intensity, road type, etc.) was provided by the traffic model developed by the Madrid City Council along with observations from field campaigns. Hourly emissions were computed for nearly 15 000 road segments distributed in 9 management areas covering the Madrid city and surroundings. Total annual NOX emissions predicted by HBEFA were a 21% higher than those of COPERT. The discrepancies for NO2 were lower (13%) since resulting average NO2/NOX ratios are lower for HBEFA. The larger differences are related to diesel vehicle emissions under "stop & go" traffic conditions, very common in distributor/secondary roads of the Madrid metropolitan area.In order to understand the representativeness of these results, the resulting emissions were integrated in an urban scale inventory used to drive mesoscale air quality simulations with the Community Multiscale Air Quality (CMAQ) modelling system (1 km2 resolution). Modelled NO2 concentrations were compared with observations through a series of statistics. Although there are no remarkable differences between both model runs, the results suggest that HBEFA may overestimate traffic emissions. However, the results are strongly influenced by methodological issues and limitations of the traffic model. This study was useful to provide a first alternative estimate to the official emission inventory in Madrid and to identify the main features of the traffic model that should be improved to support the application of an emission system based on "real world" emission factors.

  12. Emissions from miombo woodland and dambo grassland savanna fires

    NASA Astrophysics Data System (ADS)

    Sinha, Parikhit; Hobbs, Peter V.; Yokelson, Robert J.; Blake, Donald R.; Gao, Song; Kirchstetter, Thomas W.

    2004-06-01

    Airborne measurements of trace gases and particles over and downwind of two prescribed savanna fires in Zambia are described. The measurements include profiles through the smoke plumes of condensation nucleus concentrations and normalized excess mixing ratios of particles and gases, emission factors for 42 trace gases and seven particulate species, and vertical profiles of ambient conditions. The fires were ignited in plots of miombo woodland savanna, the most prevalent savanna type in southern Africa, and dambo grassland savanna, an important enclave of miombo woodland ecosystems. Emission factors for the two fires are combined with measurements of fuel loading, combustion factors, and burned area (derived from satellite burn scar retrievals) to estimate the emissions of trace gases and particles from woodland and grassland savanna fires in Zambia and southern Africa during the dry season (May-October) of 2000. It is estimated that the emissions of CO2, CO, total hydrocarbons, nitrogen oxides (NOx as NO), sulfur dioxide (SO2), formaldehyde, methyl bromide, total particulate matter, and black carbon from woodland and grassland savanna fires during the dry season of 2000 in southern Africa contributed 12.3%, 12.6%, 5.9%, 10.3%, 7.5%, 24.2%, 2.8%, 17.5%, and 11.1%, respectively, of the average annual emissions from all types of savanna fires worldwide. In 2000 the average annual emissions of methane, ethane, ethene, acetylene, propene, formaldehyde, methanol, and acetic acid from the use of biofuels in Zambia were comparable to or exceeded dry season emissions of these species from woodland and grassland savanna fires in Zambia.

  13. Emissions from Miombo Woodland and Dambo Grassland Savanna Fires

    NASA Technical Reports Server (NTRS)

    Sinha, Parikhit; Hobbs, Peter V.; Yokelson, Robert J.; Blake, Donald R.; Gao, Song; Kirchstetter, Thomas W.

    2004-01-01

    Airborne measurements of trace gases and particles over and downwind of two prescribed savanna fires in Zambia are described. The measurements include profiles through the smoke plumes of condensation nucleus concentrations and normalized excess mixing ratios of particles and gases, emission factors for 42 trace gases and seven particulate species, and vertical profiles of ambient conditions. The fires were ignited in plots of miombo woodland savanna, the most prevalent savanna type in southern Africa, and dambo grassland savanna, an important enclave of miombo woodland ecosystems. Emission factors for the two fires are combined with measurements of fuel loading, combustion factors, and burned area (derived from satellite burn scar retrievals) to estimate the emissions of trace gases and particles from woodland and grassland savanna fires in Zambia and southern Africa during the dry season (May-October) of 2000. It is estimated that the emissions of CO2, CO, total hydrocarbons, nitrogen oxides (NOx as NO), sulfur dioxide (SO2), formaldehyde, methyl bromide, total particulate matter, and black carbon from woodland and grassland savanna fires during the dry season of 2000 in southern Africa contributed 12.3%, 12.6%, 5.9%, 10.3%, 7.5%, 24.2%, 2.8%, 17.5%, and 11.1%, respectively, of the average annual emissions from all types of savanna fires worldwide. In 2000 the average annual emissions of methane, ethane, ethene, acetylene, propene, formaldehyde, methanol, and acetic acid from the use of biofuels in Zambia were comparable to or exceeded dry season emissions of these species from woodland and grassland savanna fires in Zambia.

  14. Large emissions of perfluorocarbons in East Asia deduced from continuous atmospheric measurements.

    PubMed

    Saito, Takuya; Yokouchi, Yoko; Stohl, Andreas; Taguchi, Shoichi; Mukai, Hitoshi

    2010-06-01

    The atmospheric mixing ratios of perfluorocarbons (PFCs), extremely potent greenhouse gases, have been continuously measured at two Japanese stations (Cape Ochiishi and Hateruma Island) since 2006, to infer their global and regional emissions. The baseline mixing ratios of the measured C(2)-C(4) PFCs [PFC-116 (C(2)F(6)), PFC-218 (C(3)F(8)), and PFC-318 (c-C(4)F(8))] showed slight annual increases of 1%-3%. Enhanced mixing ratios above baseline were occasionally observed at both sites in air masses that had passed over metropolitan regions in East Asia, suggesting high PFC emissions from those regions. We applied transport models to these pollution events and an inversion technique to estimate national emissions. The results suggest that, among the studied regions (China, Japan, North Korea, South Korea, and Taiwan), China was the largest PFC emitter, accounting for more than half of the regional emissions, followed by Japan. The estimated total emissions of each PFC from East Asia were 0.86 Gg yr(-1) for PFC-116, 0.31 Gg yr(-1) for PFC-218, and 0.56 Gg yr(-1) for PFC-318. They contributed greatly to global emissions as derived from the annual increases in the baseline mixing ratios, accounting for more than 75% of global PFC-218 and PFC-318 emissions and for approximately 40% of global PFC-116 emissions. PMID:20441144

  15. Significant fraction of CO2 emissions from boreal lakes derived from hydrologic inorganic carbon inputs

    NASA Astrophysics Data System (ADS)

    Weyhenmeyer, Gesa A.; Kosten, Sarian; Wallin, Marcus B.; Tranvik, Lars J.; Jeppesen, Erik; Roland, Fabio

    2015-12-01

    Annual CO2 emissions from lakes and other inland waters into the atmosphere are estimated to almost entirely compensate the total annual carbon uptake by oceans. CO2 supersaturation in lakes, which results in CO2 emissions, is frequently attributed to CO2 produced within the lake. However, lateral inorganic carbon flux through watersheds can also be sizeable. Here we calculated lake surface water CO2 concentrations and emissions using lake pH, alkalinity and temperature from a compilation of data from 5,118 boreal lakes. Autumn surface water CO2 concentrations and CO2 emissions from the 5,118 lakes co-varied with lake internal autumn CO2 production. However, using a mass balance approach we found that CO2 emission in the majority of lakes was sustained by inorganic carbon loading from the catchment rather than by internal CO2 production. Small lakes with high dissolved organic carbon and phosphorus concentrations, shorter retention times and longer ice-free seasons had the highest CO2 concentrations. CO2 emissions from these small lakes was twice that of comparable lakes in colder regions, and similar to emissions from subtropical and tropical lakes. We conclude that changes in land use and climate that increase dissolved inorganic carbon may cause emission levels from boreal lakes to approach those of lakes in warmer regions.

  16. An Emission Inventory of Polycyclic Aromatic Hydrocarbons in China

    NASA Astrophysics Data System (ADS)

    Mu, Xilong; Zhu, Xianlei; Wang, Xuesong

    2015-04-01

    Polycyclic Aromatic Hydrocarbons (PAHs) are among the most dangerous compounds due to their high carcinogenic and mutagenic character. Emission inventory provides the primary data to account for the sources of ambient PAHs and server as a necessary database for effective PAHs pollution control. China is experiencing fast economic growth and large energy consumption, which might result in a large amount of PAHs anthropogenic emissions. Therefore, based on the previous studies and combined recently field emission measurements as well as socio-economic activity data, the development of a nationwide PAHs emission inventory is needed. In this work, the emission inventory of 16 PAHs listed as U.S. Environmental Protection Agency priority pollutants in China in the year 2012 is compiled. The emission amounts of PAHs were estimated as annual rates of emission-related activities multiplied by respective emission factors. The activities such as fuel consumption, including fossil fuel and biofuel, and socio-economic statistics were obtained from yearbook released by Chinese central government and/or provincial governments, as well as related industry reports. Emission factors were derived from the related literature. Recently reported emission factors from local measurements were used. The total emissions of PAHs were 120611 ton in 2012. In China, PAHs were emitted predominantly from domestic combustion of coal and biofuel, coking industry and motor vehicles, accounting for 72% of the total amount. PAHs emission profiles were significantly different between China and the other countries. The emission profile in China featured a relatively higher portion of high molecular weight species with carcinogenic potential due to large contributions of domestic combustion and coking industry. Domestic combustion of straw, coal and firewood emitted 19464 ton, 8831 ton, and 5062 ton of PAHs, respectively, which were much higher than those in other countries. Emission per capita showed geographical variations. In general, the southeastern provinces of China were characterized by higher emission per capita. The PAHs emissions were higher in the winter than those in the summer. In the following work, the above emission inventory will be used as an input to Chemical Transport Model to simulate the ambient PAHs concentrations in China, and the uncertainty of the inventory will be assessed based on the comparisons between simulated concentrations and available observations. Acknowledgement This work was financially supported by the Natural Science Foundation of China (Grant No. 41175102). Corresponding author: Xuesong Wang

  17. Seasonal trends of biogenic terpene emissions.

    PubMed

    Helmig, Detlev; Daly, Ryan Woodfin; Milford, Jana; Guenther, Alex

    2013-09-01

    Biogenic volatile organic compound (BVOC) emissions from six coniferous tree species, i.e. Pinus ponderosa (Ponderosa Pine), Picea pungens (Blue Spruce), Pseudotsuga menziesii (Rocky Mountain Douglas Fir) and Pinus longaeva (Bristlecone Pine), as well as from two deciduous species, Quercus gambelii (Gamble Oak) and Betula occidentalis (Western River Birch) were studied over a full annual growing cycle. Monoterpene (MT) and sesquiterpene (SQT) emissions rates were quantified in a total of 1236 individual branch enclosure samples. MT dominated coniferous emissions, producing greater than 95% of BVOC emissions. MT and SQT demonstrated short-term emission dependence with temperature. Two oxygenated MT, 1,8-cineol and piperitone, were both light and temperature dependent. Basal emission rates (BER, normalized to 1000μmolm(-2)s(-1) and 30°C) were generally higher in spring and summer than in winter; MT seasonal BER from the coniferous trees maximized between 1.5 and 6.0μgg(-1)h(-1), while seasonal lows were near 0.1μgg(-1)h(-1). The fractional contribution of individual MT to total emissions was found to fluctuate with season. SQT BER measured from the coniferous trees ranged from <0.01 to 0.15μgg(-1)h(-1). BER of up to 1.2μgg(-1)h(-1) of the SQT germacrene B were found from Q. gambelii, peaking in late summer. The β-factor, used to define temperature dependence in emissions modeling, was not found to exhibit discernible growth season trends. A seasonal correction factor proposed by others in previous work to account for a sinusoidal shaped emission pattern was applied to the data. Varying levels of agreement were found between the data and model results for the different plant species seasonal data sets using this correction. Consequently, the analyses on this extensive data set suggest that it is not feasible to apply a universal seasonal correction factor across different vegetation species. A modeling exercise comparing two case scenarios, (1) without and (2) with consideration of the seasonal changes in emission factors illustrated large deviations when emission factors are applied for other seasons than those in which they were experimentally determined. PMID:23827483

  18. LLNL NESHAPs 2014 Annual Report

    SciTech Connect

    Wilson, K.; Bertoldo, N.; Gallegos, G.; MacQueen, D.; Wegrecki, A.

    2015-07-01

    Lawrence Livermore National Security, LLC operates facilities at Lawrence Livermore National Laboratory (LLNL) where radionuclides are handled and stored. These facilities are subject to the U.S. Environmental Protection Agency (EPA) National Emission Standards for Hazardous Air Pollutants (NESHAPs) in Code of Federal Regulations (CFR) Title 40, Part 61, Subpart H, which regulates radionuclide emissions to air from Department of Energy (DOE) facilities. Specifically, NESHAPs limits the emission of radionuclides to the ambient air to levels resulting in an annual effective dose equivalent of 10 mrem (100 μSv) to any member of the public. Using measured and calculated emissions, and building-specific and common parameters, LLNL personnel applied the EPA-approved computer code, CAP88-PC, Version 4.0.1.17, to calculate the dose to the maximally exposed individual member of the public for the Livermore Site and Site 300.

  19. Sulfur hexafluoride (SF6) emissions in East Asia determined by inverse modeling

    NASA Astrophysics Data System (ADS)

    Fang, X.; Thompson, R. L.; Saito, T.; Yokouchi, Y.; Kim, J.; Li, S.; Kim, K. R.; Park, S.; Graziosi, F.; Stohl, A.

    2013-08-01

    Sulfur hexafluoride (SF6) has a global warming potential of around 22 800 over a 100 yr time horizon and is one of the greenhouse gases regulated under the Kyoto Protocol. Around circa 2000 there was a reversal in the global SF6 emission trend, from a decreasing to an increasing trend, which was likely caused by increasing emissions in countries that are not obligated to report their annual emissions to the United Nations Framework Convention on Climate Change. In this study, SF6 emissions during the period 2006-2012 for all East Asian countries, including Mongolia, China, the Taiwan region, North Korea, South Korea and Japan, were determined by using inverse modeling and in-situ atmospheric measurements. We found that the most important sources of uncertainty associated with these inversions are related to the choice of a priori emissions and their assumed uncertainty, the station network as well as the meteorological input data. Much lower uncertainties are due to seasonal variability in the emissions, inversion geometry and resolution, and the measurement calibration scale. Based on the results of these sensitivity tests, we estimate that the total SF6 emission in East Asia increased rapidly from 2437 ± 329 Mg yr-1 in 2006 to 3787 ± 512 Mg yr-1 in 2009 and stabilized thereafter. China contributed 58-72 % to the total East Asian emission for the different years, followed by South Korea (9-19%), Japan (5-16%) and the Taiwan region (4-7%), while the contributions from North Korea and Mongolia together were less than 3% of the total. The per-capita SF6 emissions are highest in South Korea and the Taiwan region, while the per-capita emissions for China, North Korea and Japan are close to global average. During the period 2006-2012, emissions from China increased rapidly and emissions from South Korea increased slightly, while emissions from the Taiwan region and Japan decreased overall.

  20. 35th Annual Official Education Construction Report

    ERIC Educational Resources Information Center

    Agron, Joe

    2009-01-01

    Spending on construction by the nation's education institutions increased in 2008, reversing four years of declines in total annual expenditures, according to "American School & University"'s 35th annual Official Education Construction Report. One of the reasons for the increase in spending was the fact that the majority of the construction…

  1. 77 FR 16484 - Annual Stress Test

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-03-21

    ... in the ] proposed rule.\\2\\ Please submit your comments using only one method. \\2\\ See 77 FR 3166... CORPORATION 12 CFR Part 325 RIN 3064-AD91 Annual Stress Test AGENCY: Federal Deposit Insurance Corporation... Corporation with total consolidated assets of more than $10 billion to conduct annual stress tests. \\1\\...

  2. 78 FR 68023 - Annual Wholesale Trade Survey

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-11-13

    ... collect data covering annual sales, e- commerce sales, purchases, total operating expenses, year-end... Census Bureau will collect data covering sales, e-commerce sales, year-end inventories held inside and... offices, the Census Bureau will collect data covering annual sales, e-commerce sales, year-end...

  3. 75 FR 63805 - Annual Wholesale Trade Survey

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-10-18

    ... Census Bureau will collect data on annual sales, e-commerce sales, purchases, total operating expenses... wholesale distributors, the Census Bureau will collect data covering sales, e-commerce sales, year-end... manufacturers' sales branches and offices, the Census Bureau will collect data covering annual sales,...

  4. 76 FR 64894 - Annual Wholesale Trade Survey

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-10-19

    ... collect data covering annual sales, e-commerce sales, purchases, total operating expenses, year-end..., e- commerce sales, year-end inventories held inside and outside the United States, purchases, and... data covering annual sales, e-commerce sales, year-end inventories held inside and outside the...

  5. A multitower measurement network estimate of California's methane emissions

    NASA Astrophysics Data System (ADS)

    Jeong, Seongeun; Hsu, Ying-Kuang; Andrews, Arlyn E.; Bianco, Laura; Vaca, Patrick; Wilczak, James M.; Fischer, Marc L.

    2013-10-01

    present an analysis of methane (CH4) emissions using atmospheric observations from five sites in California's Central Valley across different seasons (September 2010 to June 2011). CH4 emissions for spatial regions and source sectors are estimated by comparing measured CH4 mixing ratios with transport model (Weather Research and Forecasting and Stochastic Time-Inverted Lagrangian Transport) predictions based on two 0.1° CH4 (seasonally varying "California-specific" (California Greenhouse Gas Emission Measurements, CALGEM) and a static global (Emission Database for Global Atmospheric Research, release version 42, EDGAR42)) prior emission models. Region-specific Bayesian analyses indicate that for California's Central Valley, the CALGEM- and EDGAR42-based inversions provide consistent annual total CH4 emissions (32.87 ± 2.09 versus 31.60 ± 2.17 Tg CO2eq yr-1; 68% confidence interval (CI), assuming uncorrelated errors between regions). Summing across all regions of California, optimized CH4 emissions are only marginally consistent between CALGEM- and EDGAR42-based inversions (48.35 ± 6.47 versus 64.97 ± 11.85 Tg CO2eq), because emissions from coastal urban regions (where landfill and natural gas emissions are much higher in EDGAR than CALGEM) are not strongly constrained by the measurements. Combining our results with those from a recent study of the South Coast Air Basin narrows the range of estimates to 43-57 Tg CO2eq yr-1 (1.3-1.8 times higher than the current state inventory). These results suggest that the combination of rural and urban measurements will be necessary to verify future changes in California's total CH4 emissions.

  6. LLNL NESHAPs 2008 Annual Report

    SciTech Connect

    Bertoldo, N; Gallegos, G; MacQueen, D; Wegrecki, A; Wilson, K

    2009-06-25

    Lawrence Livermore National Security, LLC operates facilities at Lawrence Livermore National Laboratory (LLNL) where radionuclides are handled and stored. These facilities are subject to the U.S. Environmental Protection Agency (EPA) National Emission Standards for Hazardous Air Pollutants (NESHAPs) in Code of Federal Regulations (CFR) Title 40, Part 61, Subpart H, which regulates radionuclide emissions to air from Department of Energy (DOE) facilities. Specifically, NESHAPs limits the emission of radionuclides to the ambient air to levels resulting in an annual effective dose equivalent of 10 mrem (100 {mu}Sv) to any member of the public. Using measured and calculated emissions, and building-specific and common parameters, LLNL personnel applied the EPA-approved computer code, CAP88-PC, Version 1.0, to calculate the dose to the maximally exposed individual for the Livermore site and Site 300. The dose for the LLNL site-wide maximally exposed members of the public from operations in 2008 are summarized here: {sm_bullet} Livermore site: 0.0013 mrem (0.013 {mu}Sv) (26% from point source emissions, 74% from diffuse source emissions). The point source emissions include gaseous tritium modeled as tritiated water vapor as directed by EPA Region IX; the resulting dose is used for compliance purposes. {sm_bullet} Site 300: 0.000000044 mrem (0.00000044 {mu}Sv) (100% from point source emissions).

  7. Relative Contributions of Soil, Foliar and Woody-Tissue Respiration to Total Ecosystem Respiration in Different-Age Planted Forests

    NASA Astrophysics Data System (ADS)

    Khomik, M.; Arain, A. M.; Peichl, M.; Restrepo-Coupe, N.; McLaren, J. D.; Brodeur, J.

    2009-05-01

    Forest ecosystem respiration (Re) consists of smaller components, such as soil (Rs), foliar (Rf), and woody tissue (Rw) respiration, which function at different temporal and spatial scales. An understading the seasonal dynamics and intersite variability of these component fluxes is necessary to properly quantify Re in space and time. We measured CO2 emissions from soil, foliage, and woody-tissue in temperate, planted, white pine (Pinus Strobus L.) forests, aged: 70-, 35-, 20- and 7-years-old, using a portable chamber system. Empirical models were used to compute daily emissions from each Re component. These emissions were upscaled to stand level, using biometric indecies, and summed-up to estimate monthly and annual Re for each forest stand. The relative percent contribution of each component to total annual Re varied among the stands. Rs dominated emissions at the youngest stand, while Rf dominated emissions at the 20-year-old stand. In contrast, at the two oldest stands, Rs and Rf were comparable. Rs was 44, 40, 29, and 69 % of Re, across the 70-, 35-, 20-, and 7-year-old stands, while Rf accounted for 48, 40, 58, and 31 % of Re, respectively. Rw was the smallest component of annual Re across the stands (9, 15, 13 and 0.1 %, respectively). In general, Re increased up to and peaked around age 20, then decreased somewhat for the older stands. However, within ± 2 standard deviations on the sum, Re at the 20-year-old stand was comparable to that of the 70-year-old stand and higher than that of the 35-year-old stand. Differences in past land-use history and growth stage of these plantations may have been responsible for the observed trends in Re and its components. Our results highlight the need to consider component fluxes, as well as stand characteristics, prior, during, and after afforestation, when assessing annual carbon budgets of planted forests.

  8. How do emission patterns in megacities affect regional air pollution?

    NASA Astrophysics Data System (ADS)

    Heil, A.; Richter, C.; Schroeder, S.; Schultz, M. G.

    2010-12-01

    Megacities around the world show distinctly different emission patterns in terms of absolute amounts and emission ratios of individual chemical compounds due to varying socio-economic developments and technological standards. The emission patterns influence the chemical reactivity of the urban pollution plume, and hence determine air quality in and around megacity areas. In this study, which is part of the European project CITYZEN (megaCITY - Zoom for the ENvironment), the effects of emission changes in four selected megacity areas on air pollution were investigated: BeNeLux (BNL), Istanbul (IST), Pearl River Delta (PRD) and Sao Paulo (SAP). The study aims at answering the question: how would air pollution in megacity X change if it had the same urban emissions per capita as megacity Y? Model simulations with the global chemistry climate model ECHAM5-MOZ were carried out for the year 2001 using a resolution of about 2 degrees in the horizontal and of 31 levels (surface to 10 hPa) in the vertical. The model was driven by meteorological input data from the ECMWF ERA Interim reanalysis. Emissions were taken from the gridded global ACCMIP emission inventory recently established for use in chemistry-climate simulations in connection to the IPCC-AR5 assessments (Lamarque et al. 2010). We carried out sensitivity simulations where emission patterns from each of the megacity areas were replaced by those from all others. This was done on the basis of the per capita emissions for each species and sector averaged over the respective region. Total per capita CO and NMVOC emissions are highest in PRD and lowest in SAP while total per capita NOx emissions are highest in BNL and lowest in SAP. There are strong differences in the relative contribution of the urban sectors to total emissions of individual compounds. As a result, each of the four megacity areas exhibits a very characteristic NMVOC speciation profile which determines the NMVOC-related photochemical ozone (O_3) creation potential. Compared to the emissions used in the reference simulation, changing per capita urban emissions in BNL into those of IST or SAP will lead to reduction in total megacity emissions of CO and NOx by between 40 to 80% and of between 5 to 20% for NMVOC. When the per capita emissions for PRD are applied, only NOx decreases (by 50%) while CO and NMVOC increase by between 20 and 40%. Similar changes occur when the emissions are interchanged in the other three regions. Annual mean ambient O_3 concentrations in the entire BNL megacity domain are elevated by 3 to 8 ppb in all sensitivity runs and a significant effect is also found outside the main megacity area. In the IST and PRD megacity areas, O_3 levels increase or decrease by 1 to 5 ppb when the per capita emissions from the other regions are used. For the SAP megacity area, all scenarios lead to a reduction of annual mean O_3 levels by more than 4 ppb in the north-western section of the domain while increases up to 3 ppb are predicted for some southern regions. We will also present an analysis of changes in the photochemical regimes related to altered emission patterns. The study can contribute directly to the development of air pollution abatement strategies.

  9. Emissions Of Greenhouse Gases From Rice Agriculture

    SciTech Connect

    M. Aslam K. Khalil

    2009-07-16

    This project produced detailed data on the processes that affect methane and nitrous oxide emissions from rice agriculture and their inter-relationships. It defines the shifting roles and potential future of these gases in causing global warming and the benefits and tradeoffs of reducing emissions. The major results include: 1). Mechanisms and Processes Leading to Methane Emissions are Delineated. Our experiments have tested the standard model of methane emissions from rice fields and found new results on the processes that control the flux. A mathematical mass balance model was used to unravel the production, oxidation and transport of methane from rice. The results suggested that when large amounts of organic matter are applied, the additional flux that is observed is due to both greater production and reduced oxidation of methane. 2). Methane Emissions From China Have Been Decreasing Over the Last Two Decades. We have calculated that methane emissions from rice fields have been falling in recent decades. This decrease is particularly large in China. While some of this is due to reduced area of rice agriculture, the bigger effect is from the reduction in the emission factor which is the annual amount of methane emitted per hectare of rice. The two most important changes that cause this decreasing emission from China are the reduced use of organic amendments which have been replaced by commercial nitrogen fertilizers, and the increased practice of intermittent flooding as greater demands are placed on water resources. 3). Global Methane Emissions Have Been Constant For More Than 20 Years. While the concentrations of methane in the atmosphere have been leveling off in recent years, our studies show that this is caused by a near constant total global source of methane for the last 20 years or more. This is probably because as some anthropogenic sources have increased, others, such as the rice agriculture source, have fallen. Changes in natural emissions appear small. 4). Nitrous Oxide Emissions From Rice Fields Increase as Methane Emissions Drop. Inundated conditions favor anaerobic methane production with high emission rates and de-nitrification resulting in modest nitrous oxide emissions. Under drier conditions such as intermittent flooding, methane emissions fall and nitrous oxide emissions increase. Increased nitrogen fertilizer use increases nitrous oxide emissions and is usually accompanied by reduced organic matter applications which decreases methane emissions. These mechanisms cause a generally inverse relationship between methane and nitrous oxide emissions. Reduction of methane from rice agriculture to control global warming comes with tradeoffs with increased nitrous oxide emissions. 5). High Spatial Resolution Maps of Emissions Produced. Maps of methane and nitrous oxide emissions at a resolution of 5 min × 5 min have been produced based on the composite results of this research. These maps are necessary for both scientific and policy uses.

  10. Greenhouse gas emissions from shifting cultivation in the tropics, including uncertainty and sensitivity analysis

    NASA Astrophysics Data System (ADS)

    Silva, J. M. N.; Carreiras, J. M. B.; Rosa, I.; Pereira, J. M. C.

    2011-10-01

    Annual emissions of CO2, CH4, CO, N2O, and NOx from biomass burning in shifting cultivation systems in tropical Asia, Africa, and America were estimated at national and continental levels as the product of area burned, aboveground biomass, combustion completeness, and emission factor. The total area of shifting cultivation in each country was derived from the Global Land Cover 2000 map, while the area cleared and burned annually was obtained by multiplying the total area by the rotation cycle of shifting cultivation, calculated using cropping and fallow lengths reported in the literature. Aboveground biomass accumulation was estimated as a function of the duration and mean temperature of the growing season, soil texture type, and length of the fallow period. The uncertainty associated with each model variable was estimated, and an uncertainty and sensitivity analysis of greenhouse gas estimates was performed with Monte Carlo and variance decomposition techniques. Our results reveal large uncertainty in emission estimates for all five gases. In the case of CO2, mean (standard deviation) emissions from shifting cultivation in Asia, Africa, and America were estimated at 241 (132), 205 (139), and 295 (197) Tg yr-1, respectively. Combustion completeness and emission factors were the model inputs that contributed the most to the uncertainty of estimates. Our mean estimates are lower than the literature values for atmospheric emission from biomass burning in shifting cultivation systems. Only mean values could be compared since other studies do not provide any measure of uncertainty.

  11. Characterization of gas and particle emissions from laboratory burns of peat

    NASA Astrophysics Data System (ADS)

    Black, Robert R.; Aurell, Johanna; Holder, Amara; George, Ingrid J.; Gullett, Brian K.; Hays, Michael D.; Geron, Chris D.; Tabor, Dennis

    2016-05-01

    Peat cores collected from two locations in eastern North Carolina (NC, USA) were burned in a laboratory facility to characterize emissions during simulated field combustion. Particle and gas samples were analyzed to quantify emission factors for particulate matter (PM2.5), organic carbon (OC), elemental carbon, light absorbing carbon, absorption Angstrom exponent, metals, polycyclic aromatic hydrocarbons (PAHs), and polychlorinated dibenzodioxins/dibenzofurans (PCDDs/PCDFs). CO from the smoldering burns, up to 7 h in duration, contributed approximately 16% of the total carbon emitted. Emission factors for black carbon (BC) and light absorbing carbon (UVPM) were considerably lower than those found for forest litter burns. Emission factors for PCDDs/PCDFs were near published values for forest fuels, at 1-4 ng toxic equivalents (TEQ)/kg carbon burned (Cb). Total PAH concentrations of ≥12 mg/kg were higher than published data from biomass burns, but roughly the same in terms of toxicity. Application of these emission factors to the noteworthy 2008 "Evans Road" fire in NC indicates that PM2.5 and PCDD/PCDF emissions from this fire may have been 4-6% of the annual US inventory and 5% of the annual OC amount.

  12. How important are atmospheric depressions and nocturnal low-level jets for North African dust emission?

    NASA Astrophysics Data System (ADS)

    Fiedler, Stephanie; Schepanski, Kerstin; Knippertz, Peter; Heinold, Bernd; Tegen, Ina

    2014-05-01

    Nocturnal low-level jets (NLLJs) and atmospheric depressions are known to generate wind speeds sufficient for dust emission in North Africa, but their relative importance is not well quantified. This work presents the first climatology of dust emission associated with theses phenomenon based on ERA-Interim data from the European Centre for Medium-Range Weather Forecasts. Depressions are detected as minima in the geopotential height at 925 hPa with a tracking algorithm. NLLJs are identified with a new automated detection algorithm. The results of the identification are connected with dust emissions from a dust model driven by 10m-winds from ERA-Interim. The findings highlight that atmospheric depressions are associated with 55 % of the dust emission in the annual and spatial mean. Regions south of the Atlas Mountains in spring and wide areas of North Africa during summer have contributions of up to 90 %. Lee cyclogenesis causes favourable conditions predominantly in spring while the heat low over West Africa dominates the climatology in summer. Migrating cyclones that live for more than two days are rare and associated with 4 % of the dust emission annually and spatially averaged. Maximum contributions of cyclones to dust emission are 25 % over eastern North Africa in spring. This result suggests that few depressions forming near the Atlas Mountains undergo the development to a long-lived and moving cyclone. Even though their total contribution to dust emission is small, the emission intensity is large. The climatological mean of the emission flux is exceeded by a factor of four to eight during cyclones. The presence of soil moisture during cyclones suppresses 10 % of the dust emission. The daytime fluxes are three to five times larger than at night. NLLJs are wind speed maxima at night that build at a few 100 m above the surface. Annually and spatially averaged, NLLJs form in 29 % of nights. Single regions and seasons, e.g. the Bodélé Depression in winter and the margins of the Saharan heat low in summer, have frequencies of up to 80 %. The NLLJ contribution to the dust emission amount is 15 % annually and spatially averaged. Specific regions and seasons show NLLJ contributions of up to 60 %. The largest dust emission associated with NLLJs is found during the mid-morning when the surface inversion decays. In conclusion, atmospheric depressions, migrating cyclones and NLLJs are important for North African dust emission. This climatology enables a process-based evaluation of meteorological drivers of dust emission in atmospheric models that contributes to reducing uncertainty.

  13. Aircraft-Based Measurements of Point Source Methane Emissions in the Barnett Shale Basin.

    PubMed

    Lavoie, Tegan N; Shepson, Paul B; Cambaliza, Maria O L; Stirm, Brian H; Karion, Anna; Sweeney, Colm; Yacovitch, Tara I; Herndon, Scott C; Lan, Xin; Lyon, David

    2015-07-01

    We report measurements of methane (CH4) emission rates observed at eight different high-emitting point sources in the Barnett Shale, Texas, using aircraft-based methods performed as part of the Barnett Coordinated Campaign. We quantified CH4 emission rates from four gas processing plants, one compressor station, and three landfills during five flights conducted in October 2013. Results are compared to other aircraft- and surface-based measurements of the same facilities, and to estimates based on a national study of gathering and processing facilities emissions and 2013 annual average emissions reported to the U.S. EPA Greenhouse Gas Reporting Program (GHGRP). For the eight sources, CH4 emission measurements from the aircraft-based mass balance approach were a factor of 3.2-5.8 greater than the GHGRP-based estimates. Summed emissions totaled 7022 ± 2000 kg hr(-1), roughly 9% of the entire basin-wide CH4 emissions estimated from regional mass balance flights during the campaign. Emission measurements from five natural gas management facilities were 1.2-4.6 times larger than emissions based on the national study. Results from this study were used to represent "super-emitters" in a newly formulated Barnett Shale Inventory, demonstrating the importance of targeted sampling of "super-emitters" that may be missed by random sampling of a subset of the total. PMID:26148549

  14. Gridded atmospheric emission inventory of 2,3,7,8-TCDD in China

    NASA Astrophysics Data System (ADS)

    Huang, Tao; Tian, Chongguo; Zhang, Kai; Gao, Hong; Li, Yi-Fan; Ma, Jianmin

    2015-05-01

    Establishment of the dioxins emission inventory has been considered as a crucial step toward risk assessment and elimination of dioxins contaminations. Based on a total dioxin emission inventory in China from different emission categories in 2004, this study created a gridded emission inventory of 2,3,7,8-TCDD, the most toxic congener in dioxins, in China in 2009 with a 1/4° longitude by 1/4° latitude resolution. It was estimated that annually total 371 ± 53 g (average ± standard deviation) of 2,3,7,8-TCDD was released into the atmosphere in 2009 over China, increasing approximately by 37% compared with its emission in 2004. Differing from most developed countries where municipal waste incinerations were regarded as a major atmospheric emission source, in China ferrous and non-ferrous metal production made the largest contribution to 2,3,7,8-TCDD air emission (138 ± 16 g), followed by waste incineration (109 ± 12 g), power and heating generation (62 ± 9 g), and production of mineral products (47 ± 8 g). The rest of sources contributed approximately 3% to the total 2,3,7,8-TCDD emission in 2009. Iron and steel industries are mainly located in Beijing-Tianjin-Hebei (BTH) and Yangtze River Delta (YRD) regions, whereas waste incinerators are mainly located in Pearl River Delta (PRD) region. Higher 2,3,7,8-TCDD emissions were found in these three regions. While the BTH, YRD, and PRD accounted for only about 4% of total land area of China, they contributed approximately 14%, 15%, and 5% to the total 2,3,7,8-TCDD emission in 2009 in China, respectively.

  15. Direct Continuous Measurements of Methane Emissions from a Landfill: Method, Station and Latest Results

    NASA Astrophysics Data System (ADS)

    Burba, G. G.; Xu, L.; Lin, X.; Amen, J.; Welding, K.; McDermitt, D. K.

    2014-12-01

    Solar-powered automated flux station was deployed continuously inside the Bluff Road Landfill (Lincoln, NE) for the period of over4 years starting June 2010. Landfill methane emissions were measured using the eddy covariance method, reporting hourly emission rates. The data shown in this presentation are from the period of June to December 2010 when no gas recovery was in operation. The continuous measurements of hourly emission rates allowed a number of important analyses of the key factors affecting landfill methane emissions at different time scales. In particular, the results show that landfill methane emissions strongly depended on changes in barometric pressure. Rising barometric pressure suppressed the emission, while falling barometric pressure enhanced the emission, resulting in up to a 35-fold variation in day-to-day methane emissions. Wavelet coherence analysis revealed a strong spectral coherency between variations of barometric pressure and methane emission at periodicities ranging from 1 day to 8 days. Power spectrum and ogive analysis showed that at least 10 days of continuous measurements was needed in order to capture 90% of the total variance in the methane emission time series at the site.From these results, it is apparent that point-in-time measurements taken at monthly or longer time intervals using techniques such as the trace plume method, the mass balance method, or the closed-chamber method will be subject to large variations in measured emission rates because of the barometric pumping phenomenon. Estimates of long-term integrated methane emissions based on such measurements could yield uncertainties, ranging from 28% underestimation to 32% overestimation.The results demonstrate a need for continuous measurements to quantify annual total landfill emissions. This conclusion may also apply to the wetlands, peatlands, lakes, and other environments where emissions are from porous media or ebullition.

  16. Does extreme precipitation intensity depend on the emissions scenario?

    NASA Astrophysics Data System (ADS)

    Pendergrass, Angeline G.; Lehner, Flavio; Sanderson, Benjamin M.; Xu, Yangyang

    2015-10-01

    The rate of increase of global-mean precipitation per degree global-mean surface temperature increase differs for greenhouse gas and aerosol forcings and across emissions scenarios with differing composition of change in forcing. We investigate whether or not the rate of change of extreme precipitation also varies across the four emissions scenarios that force the Coupled Model Intercomparison Project, version 5 multimodel ensemble. In most models, the rate of increase of maximum annual daily precipitation per degree global warming in the multimodel ensemble is statistically indistinguishable across the four scenarios, whether this extreme precipitation is calculated globally, over all land, or over extratropical land. These results indicate that in contrast to mean precipitation, extreme precipitation depends on the total amount of warming and does not depend on emissions scenario in most models.

  17. A temporally and spatially resolved ammonia emission inventory for dairy cows in the United States

    NASA Astrophysics Data System (ADS)

    Pinder, Robert W.; Strader, Ross; Davidson, Cliff I.; Adams, Peter J.

    Previous inventories of ammonia emissions for the United States have not characterized the seasonal and geographic variations that are necessary for accurately predicting ambient concentrations of ammonium nitrate and ammonium sulfate aerosol. This research calculates the seasonal and geographic variation in ammonia emissions from dairy cows in the United States. Monthly, county-level emission factors are calculated with a process-based model of dairy farm emissions, the national distribution of farming practices, seasonal climate conditions, and animal populations. Annual, county-level emission factors are estimated to range between 13.1 and 55.5, with a national average of 23.9 kg NH 3 cow -1 yr -1. The seasonal variation of the emission factor is estimated to be as high as a factor of seven in some counties. Emissions are predicted to be the highest in the spring and fall, because of high manure application rates during the spring planting and after the fall harvest. Summer emissions are higher than winter, resulting from the temperature dependence of housing and storage emissions. In the summer and winter, the majority of emissions are from animal housing. In the spring and fall, the majority of emissions are from field applied manure. The 5% and 95% confidence interval about the national annual average emission factor is between 18 and 36 kg NH 3 cow -1 yr -1. Uncertainties in farming practices contribute most to the total uncertainty, yet uncertainty in the timing of manure application, the quantity of manure and nitrogen excreted by cows, and the physical processes of volatilization affecting applied manure are also significant.

  18. PROCEDURE FOR ESTIMATING PERMANENT TOTAL ENCLOSURE COSTS

    EPA Science Inventory

    The paper discusses a procedure for estimating permanent total enclosure (PTE) costs. (NOTE: Industries that use add-on control devices must adequately capture emissions before delivering them to the control device. One way to capture emissions is to use PTEs, enclosures that mee...

  19. Sulfur hexafluoride (SF6) emissions in East Asia determined by inverse modeling

    NASA Astrophysics Data System (ADS)

    Fang, X.; Thompson, R. L.; Saito, T.; Yokouchi, Y.; Kim, J.; Li, S.; Kim, K. R.; Park, S.; Graziosi, F.; Stohl, A.

    2014-05-01

    Sulfur hexafluoride (SF6) has a global warming potential of around 22 800 over a 100-year time horizon and is one of the greenhouse gases regulated under the Kyoto Protocol. Around the year 2000 there was a reversal in the global SF6 emission trend, from a decreasing to an increasing trend, which was likely caused by increasing emissions in countries that are not obligated to report their annual emissions to the United Nations Framework Convention on Climate Change. In this study, SF6 emissions during the period 2006-2012 for all East Asian countries - including Mongolia, China, Taiwan, North Korea, South Korea and Japan - were determined by using inverse modeling and in situ atmospheric measurements. We found that the most important sources of uncertainty associated with these inversions are related to the choice of a priori emissions and their assumed uncertainty, the station network as well as the meteorological input data. Much lower uncertainties are due to seasonal variability in the emissions, inversion geometry and resolution, and the measurement calibration scale. Based on the results of these sensitivity tests, we estimate that the total SF6 emission in East Asia increased rapidly from 2404 ± 325 Mg yr-1 in 2006 to 3787 ± 512 Mg yr-1 in 2009 and stabilized thereafter. China contributed 60-72% to the total East Asian emission for the different years, followed by South Korea (8-16%), Japan (5-16%) and Taiwan (4-7%), while the contributions from North Korea and Mongolia together were less than 3% of the total. The per capita SF6 emissions are highest in South Korea and Taiwan, while the per capita emissions for China, North Korea and Japan are close to global average. During the period 2006-2012, emissions from China and from South Korea increased, while emissions from Taiwan and Japan decreased overall.

  20. Coal industry annual 1993

    SciTech Connect

    Not Available

    1994-12-06

    Coal Industry Annual 1993 replaces the publication Coal Production (DOE/FIA-0125). This report presents additional tables and expanded versions of tables previously presented in Coal Production, including production, number of mines, Productivity, employment, productive capacity, and recoverable reserves. This report also presents data on coal consumption, coal distribution, coal stocks, coal prices, coal quality, and emissions for a wide audience including the Congress, Federal and State agencies, the coal industry, and the general public. In addition, Appendix A contains a compilation of coal statistics for the major coal-producing States. This report does not include coal consumption data for nonutility Power Producers who are not in the manufacturing, agriculture, mining, construction, or commercial sectors. This consumption is estimated to be 5 million short tons in 1993.

  1. The global distribution of ammonia emissions from seabird colonies

    NASA Astrophysics Data System (ADS)

    Riddick, S. N.; Dragosits, U.; Blackall, T. D.; Daunt, F.; Wanless, S.; Sutton, M. A.

    2012-08-01

    Seabird colonies represent a significant source of atmospheric ammonia (NH3) in remote maritime systems, producing a source of nitrogen that may encourage plant growth, alter terrestrial plant community composition and affect the surrounding marine ecosystem. To investigate seabird NH3 emissions on a global scale, we developed a contemporary seabird database including a total seabird population of 261 million breeding pairs. We used this in conjunction with a bioenergetics model to estimate the mass of nitrogen excreted by all seabirds at each breeding colony. The results combined with the findings of mid-latitude field studies of volatilization rates estimate the global distribution of NH3 emissions from seabird colonies on an annual basis. The largest uncertainty in our emission estimate concerns the potential temperature dependence of NH3 emission. To investigate this we calculated and compared temperature independent emission estimates with a maximum feasible temperature dependent emission, based on the thermodynamic dissociation and solubility equilibria. Using the temperature independent approach, we estimate global NH3 emissions from seabird colonies at 404 Gg NH3 per year. By comparison, since most seabirds are located in relatively cold circumpolar locations, the thermodynamically dependent estimate is 136 Gg NH3 per year. Actual global emissions are expected to be within these bounds, as other factors, such as non-linear interactions with water availability and surface infiltration, moderate the theoretical temperature response. Combining sources of error from temperature (±49%), seabird population estimates (±36%), variation in diet composition (±23%) and non-breeder attendance (±13%), gives a mid estimate with an overall uncertainty range of NH3 emission from seabird colonies of 270 [97-442] Gg NH3 per year. These emissions are environmentally relevant as they primarily occur as "hot-spots" in otherwise pristine environments with low anthropogenic emissions.

  2. Attributing land-use change carbon emissions to exported biomass

    SciTech Connect

    Saikku, Laura; Soimakallio, Sampo; Pingoud, Kim

    2012-11-15

    In this study, a simple, transparent and robust method is developed in which land-use change (LUC) emissions are retrospectively attributed to exported biomass products based on the agricultural area occupied for the production. LUC emissions account for approximately one-fifth of current greenhouse gas emissions. Increasing agricultural exports are becoming an important driver of deforestation. Brazil and Indonesia are used as case studies due to their significant deforestation in recent years. According to our study, in 2007, approximately 32% and 15% of the total agricultural land harvested and LUC emissions in Brazil and Indonesia respectively were due to exports. The most important exported single items with regard to deforestation were palm oil for Indonesia and bovine meat for Brazil. To reduce greenhouse gas (GHG) emissions effectively worldwide, leakage of emissions should be avoided. This can be done, for example, by attributing embodied LUC emissions to exported biomass products. With the approach developed in this study, controversial attribution between direct and indirect LUC and amortization of emissions over the product life cycle can be overcome, as the method operates on an average basis and annual level. The approach could be considered in the context of the UNFCCC climate policy instead of, or alongside with, other instruments aimed at reducing deforestation. However, the quality of the data should be improved and some methodological issues, such as the allocation procedure in multiproduct systems and the possible dilution effect through third parties not committed to emission reduction targets, should be considered. - Highlights: Black-Right-Pointing-Pointer CO{sub 2} emissions from land use changes are highly important. Black-Right-Pointing-Pointer Attribution of land use changes for products is difficult. Black-Right-Pointing-Pointer Simple and robust method is developed to attribute land use change emissions.

  3. Nitrous oxide and greenhouse gas emissions from grazed pastures as affected by use of nitrification inhibitor and restricted grazing regime.

    PubMed

    Luo, Jiafa; Ledgard, Stewart F; Lindsey, Stuart B

    2013-11-01

    Integration of a restricted grazing regime in winter with the use of a nitrification inhibitor can potentially reduce N2O emissions from grazed pasture systems. A three year field study was conducted to compare annual N2O emission rates from a "tight nitrogen" grazed farmlet with those from a control farmlet. The control farmlet was managed under a conventional rotational all-year grazing regime, while the "tight nitrogen" farmlet was under a similar grazing regime, except during winter and early spring seasons when cows grazed for about 6h per day. A nitrification inhibitor (dicyandiamide, DCD) was applied onto the "tight nitrogen" farmlet immediately after grazing through winter and early spring. A chamber technique was used to measure N2O emissions in several paddocks from each farmlet during three contrasting seasons each year. The IPCC (Intergovernmental Panel on Climate Change) inventory methodology was used to estimate CH4 and indirect N2O emissions and the life cycle assessment (LCA) methodology was used to calculate CO2 emissions from the farm systems. The individual and combined effects of restricted grazing and DCD use on N2O emissions were also determined. During the late spring/summer and autumn periods, N2O emission rates were generally similar between the two farmlets. The use of a restricted grazing regime and DCD reduced N2O emissions from the grazed farmlet during the winter/early spring seasons by 43-55%, 64-79% and 45-60% over each of the three years, respectively. The use of restricted grazing and DCD both resulted in a similar reduction in N2O emissions, but there was no significant further reduction from the combination of these technologies. For the three study years, the annual N2O emission rate from the "tight nitrogen" farmlet was 20% lower, on average, than from the control. Total annual greenhouse gas (GHG) emissions, however, were only 5% less in the "tight nitrogen" system. PMID:23374420

  4. Mercury emissions from waste combustion in China from 2004 to 2010

    NASA Astrophysics Data System (ADS)

    Hu, Dan; Zhang, Wei; Chen, Long; Chen, Cen; Ou, Langbo; Tong, Yindong; Wei, Wen; Long, Wenjing; Wang, Xuejun

    2012-12-01

    An inventory of mercury emissions originating from waste incineration in China, including municipal solid waste, rural household waste and agricultural waste, was calculated for the period of 2004-2010. During this period, mercury emissions from waste incineration increased at an average annual rate of 3.9%, and reached 16.6 t y-1 by the end of 2010. From 2004 to 2010, the mercury emissions from rural household waste incineration accounted for 46.6% of the total waste emissions, followed by agricultural waste (30.7%) and municipal solid waste (22.7%). However, the growth rate of mercury emissions was largest for municipal solid waste incineration, with an annual rate of 37.3%, while the emissions from rural household waste showed a negative growth rate (-5.8%). The mercury emissions from waste combustion is projected to be 18.6 t y-1 by 2015, with the contribution of municipal solid waste, rural household waste and agricultural waste being 46.4%, 27.1% and 26.5%, respectively.

  5. Total hydrocarbon analyzer evaluation study

    SciTech Connect

    Shamat, N. ); Crumpler, E. ); Roddan, A. )

    1991-10-01

    Measuring and controlling organic emissions from incineration processes has become a major environmental concern in recent years. The US Environmental Protection Agency (EPA) recently proposed a regulation for sewage sludge incinerators under section 405(d) of the Clean Water Act that will require all sludge incinerators to monitor total hydrocarbon emissions (THCs) on a continuous basis. Such a requirement would be part of National Pollutant Discharge Elimination (NPDES) permits and site-specific THC limits would be established for facilities based on a risk assessment of organic emissions. Before EPA can finalize the proposed requirement, THC monitoring must be successfully conducted in a plant environment and the system required by any final regulation must be kept in operation so that facilities can comply with their permits. The Metropolitan Waste Control Commission (MWCC) in St. Paul, Minn., and Rosemount Analytical Division in La Habre, Calif., entered into a joint agreement with EPA to demonstrate a hot' THC monitoring system to detect THCs in stack gases. The objectives of the study are to determine the feasibility of THC monitoring of sludge incinerator emissions; evaluate the long term reliability, cost of operation, and consistency of a continuous THC monitoring system in an incinerator environment; and determine the correlation of THC stack concentration to incinerator and scrubber operating conditions, carbon monoxide concentration, and specific VOC emissions.

  6. Commitment accounting of CO2 emissions

    NASA Astrophysics Data System (ADS)

    Davis, Steven J.; Socolow, Robert H.

    2014-08-01

    The world not only continues to build new coal-fired power plants, but built more new coal plants in the past decade than in any previous decade. Worldwide, an average of 89 gigawatts per year (GW yr-1) of new coal generating capacity was added between 2010 and 2012, 23 GW yr-1 more than in the 2000-2009 time period and 56 GW yr-1 more than in the 1990-1999 time period. Natural gas plants show a similar pattern. Assuming these plants operate for 40 years, the fossil-fuel burning plants built in 2012 will emit approximately 19 billion tons of CO2 (Gt CO2) over their lifetimes, versus 14 Gt CO2 actually emitted by all operating fossil fuel power plants in 2012. We find that total committed emissions related to the power sector are growing at a rate of about 4% per year, and reached 307 (with an estimated uncertainty of 192-439) Gt CO2 in 2012. These facts are not well known in the energy policy community, where annual emissions receive far more attention than future emissions related to new capital investments. This paper demonstrates the potential for ‘commitment accounting’ to inform public policy by quantifying future emissions implied by current investments.

  7. Extension of an assessment model of ship traffic exhaust emissions for particulate matter and carbon monoxide

    NASA Astrophysics Data System (ADS)

    Jalkanen, J.-P.; Johansson, L.; Kukkonen, J.; Brink, A.; Kalli, J.; Stipa, T.

    2012-03-01

    A method is presented for the evaluation of the exhaust emissions of marine traffic, based on the messages provided by the Automatic Identification System (AIS), which enable the positioning of ship emissions with a high spatial resolution (typically a few tens of metres). The model also takes into account the detailed technical data of each individual vessel. The previously developed model was applicable for evaluating the emissions of NOx, SOx and CO2. This paper addresses a substantial extension of the modelling system, to allow also for the mass-based emissions of particulate matter (PM) and carbon monoxide (CO). The presented Ship Traffic Emissions Assessment Model (STEAM2) allows for the influences of accurate travel routes and ship speed, engine load, fuel sulphur content, multiengine setups, abatement methods and waves. We address in particular the modeling of the influence on the emissions of both engine load and the sulphur content of the fuel. The presented methodology can be used to evaluate the total PM emissions, and those of organic carbon, elemental carbon, ash and hydrated sulphate. We have evaluated the performance of the extended model against available experimental data on engine power, fuel consumption and the composition-resolved emissions of PM. We have also compared the annually averaged emission values with those of the corresponding EMEP inventory, As example results, the geographical distributions of the emissions of PM and CO are presented for the marine regions of the Baltic Sea surrounding the Danish Straits.

  8. English in a Program of Total Innovation

    ERIC Educational Resources Information Center

    Knoll, Robert E.

    1970-01-01

    Explains an experimental program designed to give the student a total look at himself and his society through literature, politics, and history; a paper presented at annual convention of National Council of Teachers of English (Washington, D. C., November 28, 1969) and published in Kansas English" (February 1970). (Editor/SW)

  9. Potential Nitrous Oxide Emissions from Municipal Drinking Water

    NASA Astrophysics Data System (ADS)

    Anderson, D. E.; Thienelt, T.; Tindall, J.; McMahon, P.

    2005-12-01

    Nitrous oxide (N2O) is a potent greenhouse gas, having a global warming potential 280 times larger than carbon dioxide. Although the bulk of N2O emissions appear to be related to agricultural activity, various industrial and transportation related emissions exist as well. This study reports the discovery of a new and significant source of potential N2O emissions related to its presence in purified municipal water supplies worldwide. Multiple drinking water samples were obtained from 86 cities in the United States (US) and 44 cities in 16 countries in the Americas, Europe, Asia, and Africa. Samples ranged from 0.004 to 2μmol/L or the equivalent of 60% unsaturated to 200 times supersaturated with respect to ambient atmospheric concentration (320 ppb). Highest N2O contents were from southern US cities. Suspecting nitrification as the cause for the presence of N2O in drinking water, correlation statistics were calculated between N2O concentration and city size, geographical location, mean annual temperature, nitrate, and ammonia concentrations for the total population of samples as well as subsets based on country, water purification method, and raw water source (ground, surface, combination). The highest correlation (r=0.66, p<0.05, N=73) found was between latitude and N2O content for the subset group of large US cities using chloramines to purify water. Continuous year long sampling from a major US city indicated that variance in N2O content is remarkably low through the year within a water supply district. The annual US emission, based on this preliminary analysis, is 8x106 moles or 3.5X108 g N2O. Annual global emissions may be five times larger.

  10. An improvement on the dust emission scheme in the global aerosol-climate model ECHAM5-HAM

    NASA Astrophysics Data System (ADS)

    Cheng, T.; Peng, Y.; Feichter, J.; Tegen, I.

    2007-09-01

    Formulation of the dust emission scheme in the global aerosol-climate modeling system ECHAM5-HAM has been improved. Modifications on the surface aerodynamic roughness length, soil moisture and East-Asian soil properties are included in the parameterization, which result in a large impact on the threshold wind friction velocity for aeolian erosion and thus influence the simulated dust emission amount. The annual global mean of dust emission in the year 2000 is reduced by 76.5% and 2.2%, respectively, due to changes in the aerodynamic roughness length and the soil moisture. An inclusion of detailed East-Asian soil properties leads to an increase of 16.6% in the annual global mean of dust emission, which exhibits mainly in the arid and semi-arid areas of northern China and southern Mongolia. Reasonable values of annual global mean of dust emission, dust burden and total aerosol optical thickness can be obtained in the improved model. In addition, measurements of the surface dust concentrations are collected in dust source regions of East Asia, and verify a more realistic spatial distribution of dust emission in the improved model.

  11. Global atmospheric emissions of polycyclic aromatic hydrocarbons from 1960 to 2008 and future predictions.

    PubMed

    Shen, Huizhong; Huang, Ye; Wang, Rong; Zhu, Dan; Li, Wei; Shen, Guofeng; Wang, Bin; Zhang, Yanyan; Chen, Yuanchen; Lu, Yan; Chen, Han; Li, Tongchao; Sun, Kang; Li, Bengang; Liu, Wenxin; Liu, Junfeng; Tao, Shu

    2013-06-18

    Global atmospheric emissions of 16 polycyclic aromatic hydrocarbons (PAHs) from 69 major sources were estimated for a period from 1960 to 2030. Regression models and a technology split method were used to estimate country and time specific emission factors, resulting in a new estimate of PAH emission factor variation among different countries and over time. PAH emissions in 2007 were spatially resolved to 0.1° × 0.1° grids based on a newly developed global high-resolution fuel combustion inventory (PKU-FUEL-2007). The global total annual atmospheric emission of 16 PAHs in 2007 was 504 Gg (331-818 Gg, as interquartile range), with residential/commercial biomass burning (60.5%), open-field biomass burning (agricultural waste burning, deforestation, and wildfire, 13.6%), and petroleum consumption by on-road motor vehicles (12.8%) as the major sources. South (87 Gg), East (111 Gg), and Southeast Asia (52 Gg) were the regions with the highest PAH emission densities, contributing half of the global total PAH emissions. Among the global total PAH emissions, 6.19% of the emissions were in the form of high molecular weight carcinogenic compounds and the percentage of the carcinogenic PAHs was higher in developing countries (6.22%) than in developed countries (5.73%), due to the differences in energy structures and the disparities of technology. The potential health impact of the PAH emissions was greatest in the parts of the world with high anthropogenic PAH emissions, because of the overlap of the high emissions and high population densities. Global total PAH emissions peaked at 592 Gg in 1995 and declined gradually to 499 Gg in 2008. Total PAH emissions from developed countries peaked at 122 Gg in the early 1970s and decreased to 38 Gg in 2008. Simulation of PAH emissions from 2009 to 2030 revealed that PAH emissions in developed and developing countries would decrease by 46-71% and 48-64%, respectively, based on the six IPCC SRES scenarios. PMID:23659377

  12. Global atmospheric emissions of polycyclic aromatic hydrocarbons from 1960 to 2008 and future predictions

    PubMed Central

    Shen, Huizhong; Huang, Ye; Wang, Rong; Zhu, Dan; Li, Wei; Shen, Guofeng; Wang, Bin; Zhang, Yanyan; Chen, Yuanchen; Lu, Yan; Chen, Han; Li, Tongchao; Sun, Kang; Li, Bengang; Liu, Wenxin; Liu, Junfeng; Tao, Shu

    2013-01-01

    Global atmospheric emissions of 16 polycyclic aromatic hydrocarbons (PAHs) from 69 major sources were estimated for a period from 1960 to 2030. Regression models and a technology split method were used to estimate country and time specific emission factors, resulting in a new estimate of PAH emission factor variation among different countries and over time. PAH emissions in 2007 were spatially resolved to 0.1°× 0.1° grids based on a newly developed global high-resolution fuel combustion inventory (PKU-FUEL-2007). The global total annual atmospheric emission of 16 PAHs in 2007 was 504 Gg (331-818 Gg, as interquartile range), with residential/commercial biomass burning (60.5%), open-field biomass burning (agricultural waste burning, deforestation, and wildfire, 13.6%), and petroleum consumption by on-road motor vehicles (12.8%) as the major sources. South (87 Gg), East (111 Gg), and Southeast Asia (52 Gg) were the regions with the highest PAH emission densities, contributing half of the global total PAH emissions. Among the global total PAH emissions, 6.19% of the emissions were in the form of high molecular weight carcinogenic compounds and the percentage of the carcinogenic PAHs was higher in developing countries (6.22%) than in developed countries (5.73%), due to the differences in energy structures and the disparities of technology. The potential health impact of the PAH emissions was greatest in the parts of the world with high anthropogenic PAH emissions, because of the overlap of the high emissions and high population densities. Global total PAH emissions peaked at 592 Gg in 1995 and declined gradually to 499 Gg in 2008. Total PAH emissions from developed countries peaked at 122 Gg in the early 1970s and decreased to 38 Gg in 2008. Simulation of PAH emissions from 2009 to 2030 revealed that PAH emissions in developed and developing countries would decrease by 46-71% and 48-64%, respectively, based on the six IPCC SRES scenarios. PMID:23659377

  13. Energy Use and Carbon Dioxide Emissions from Cropland Production in the United States, 1990-2004

    SciTech Connect

    West, Tristram O.; Brandt, Craig C; Marland, Gregg; Nelson, Richard G; Hellwinckel, Chad M; De La Torre Ugarte, Daniel G

    2009-01-01

    Changes in cropland production and management influence energy consumption and emissions of CO2 from fossil-fuel combustion. A method was developed to calculate on-site and off-site energy and CO2 emissions for cropping practices in the US at the county scale. Energy consumption and emissions occur on-site from the operation of farm machinery and occur off-site from the manufacture and transport of cropland production inputs, such as fertilizers, pesticides, and agricultural lime. Estimates of fossil-fuel consumption and associated CO2 emissions for cropping practices enable (a) the monitoring of energy and emissions with changes in land management, and (b) the calculation and balancing of regional and national carbon budgets. Results indicate on-site energy use and total energy use (i.e., the sum of on-site and off-site) on US croplands in 2004 ranged from 1.6-7.9 GJ ha-1 yr-1 and from 5.5-20.5 GJ ha-1 yr-1, respectively. On-site and total CO2 emissions in 2004 ranged from 23-176 kg C ha-1 yr-1 and from 91-365 kg C ha-1 yr-1, respectively. During the period of this analysis (1990-2004), national total energy consumption for crop production ranged from 1204-1297 PJ yr-1 (Petajoule = 1 1015 Joule) with associated total fossil CO2 emissions ranging from 22.0-23.2 Tg C yr-1 (Teragram = 1 1012 gram). The annual proportion of on-site CO2 to total CO2 emissions changed depending on the diversity of crops planted. Adoption of reduced tillage practices in the US from 1990 to 2004 resulted in a net emissions reduction of 2.4 Tg C.

  14. Evaluation of Mobile Source Emissions and Trends

    NASA Astrophysics Data System (ADS)

    Dallmann, Timothy Ryan

    Mobile sources contribute significantly to air pollution problems. Relevant pollutants include numerous gaseous and particle-phase species that can affect human health, ecosystems, and climate. Accurate inventories of emissions from these sources are needed to help understand possible adverse impacts, and to develop effective air quality management strategies. Unfortunately large uncertainties persist in the understanding of mobile source emissions, and how these emissions are changing over time. This dissertation aims to evaluate long-term trends in mobile source emissions in the United States, and to make detailed measurements of emissions from present-day fleets of on-road vehicles operating in California. Long-term trends in mobile source emissions of nitrogen oxides (NO x) and fine particulate matter (PM2.5) in the United States were investigated through development of a fuel-based emission inventory. Annual emissions from on- and off-road gasoline and diesel engines were quantified for the years 1996-2006. Diesel engines were found to be the dominant mobile source of NOx and PM2.5, and on-road diesel vehicles were identified as the single largest anthropogenic source of NOx emissions in the United States as of 2005. The importance of diesel engines as a source of exhaust particulate matter emissions has led to the recent introduction of advanced emission control technologies in the United States, such as diesel particle filters (DPF), which have been required since 2007 for all new on-road heavy-duty (HD) diesel engines. In addition to national requirements for the use of such control devices on new engines, California has mandated accelerated clean-up of statewide emissions from older in-use diesel engines. The plume capture method was further applied to measure emissions from a more diverse population of trucks observed at the Caldecott tunnel in summer 2010. Emissions from hundreds of individual trucks were measured, and emission factor distributions were characterized for nitric oxide (NO), nitrogen dioxide (NO2), carbon monoxide (CO), formaldehyde, BC, as well as optical properties of the emitted particles. Emission factor distributions for all species were skewed, with a small fraction of trucks contributing disproportionately to total emissions. These findings confirm that the use of catalyzed DPF systems is leading to increased primary NO2 emissions. Absorption and scattering cross-section emission factors were used to calculate the aerosol single scattering albedo (SSA, at 532 nm) for individual truck exhaust plumes, which averaged 0.14 +/- 0.03. This value of aerosol SSA is very low compared to typical values (0.90-0.99) observed in ambient air studies. It is indicative of a strongly light-absorbing aerosol, due to the high BC emissions that are a characteristic feature of diesel exhaust PM emissions. Measurements at the Caldecott tunnel also included efforts to quantify light-duty (LD) gasoline vehicle emission factors, and further investigation of the relative contributions of on-road gasoline and diesel engines to air pollutant emissions. Measurements of CO, NOx, PM2.5, BC, and organic aerosol (OA) were made in a tunnel traffic bore where LD vehicles account for >99% of total traffic. Measured pollutant concentrations were apportioned between LD gasoline vehicles and diesel trucks, and fleet-average emission factors were quantified for LD gasoline vehicles using a carbon balance method. Diesel trucks contributed 18 +/- 3, 22 +/- 5, 44 +/- 8% of measured NOx, OA, and BC concentrations, respectively, despite accounting for <1% of total vehicles. Emission factors and overall fuel consumption for gasoline and diesel engines were used to describe the relative contributions of these sources to overall on-road vehicle emissions. Gasoline engines were found to be the dominant source of CO, an insignificant source of BC, and a relatively minor source of on-road OA emissions at urban, state, and national scales. Measurements at the Caldecott tunnel also featured use of a new high-resolution time-of-flight aerosol mass spectrometer, which was used to characterize the chemical composition of PM emitted by gasoline and diesel vehicles. Measurements of PM in the exhaust of individual HD trucks show a predominance of cyclyoalkane-derived ion signals relative to saturated alkane ion signals in the truck exhaust OA spectra, indicating that lubricating oil, rather than diesel fuel, was the dominant source of OA emitted by diesel trucks. This conclusion is supported by the presence of lubricant-derived trace elements in truck exhaust, emitted relative to total OA at levels that correspond to their weight fractions in bulk oil. Furthermore, comparison of mass spectra for sampling periods with varying levels of diesel influence found a high degree of similarity in the chemical composition of OA emitted by gasoline and diesel engines, suggesting a common lubricating oil rather than fuel-derived source for OA emissions. (Abstract shortened by UMI.).

  15. Cow power: the energy and emissions benefits of converting manure to biogas

    NASA Astrophysics Data System (ADS)

    Cullar, Amanda D.; Webber, Michael E.

    2008-07-01

    This report consists of a top-level aggregate analysis of the total potential for converting livestock manure into a domestic renewable fuel source (biogas) that could be used to help states meet renewable portfolio standard requirements and reduce greenhouse gas (GHG) emissions. In the US, livestock agriculture produces over one billion tons of manure annually on a renewable basis. Most of this manure is disposed of in lagoons or stored outdoors to decompose. Such disposal methods emit methane and nitrous oxide, two important GHGs with 21 and 310 times the global warming potential of carbon dioxide, respectively. In total, GHG emissions from the agricultural sector in the US amounted to 536 million metric tons (MMT) of carbon dioxide equivalent, or 7% of the total US emissions in 2005. Of this agricultural contribution, 51 to 118 MMT of carbon dioxide equivalent resulted from livestock manure emissions alone, with trends showing this contribution increasing from 1990 to 2005. Thus, limiting GHG emissions from manure represents a valuable starting point for mitigating agricultural contributions to global climate change. Anaerobic digestion, a process that converts manure to methane-rich biogas, can lower GHG emissions from manure significantly. Using biogas as a substitute for other fossil fuels, such as coal for electricity generation, replaces two GHG sourcesmanure and coal combustionwith a less carbon-intensive source, namely biogas combustion. The biogas energy potential was calculated using values for the amount of biogas energy that can be produced per animal unit (defined as 1000 pounds of animal) per day and the number of animal units in the US. The 95 million animal units in the country could produce nearly 1 quad of renewable energy per year, amounting to approximately 1% of the US total energy consumption. Converting the biogas into electricity using standard microturbines could produce 88 20 billion kWh, or 2.4 0.6% of annual electricity consumption in the US. Replacing coal and manure GHG emissions with the emissions from biogas would produce a net potential GHG emissions reduction of 99 59 million metric tons or 3.9 2.3% of the annual GHG emissions from electricity generation in the US.

  16. Effects of climate change on volatile organic compound emissions from soil and litter

    NASA Astrophysics Data System (ADS)

    Gray, C. M.; Fierer, N.

    2012-12-01

    Our knowledge of the variability and magnitude of volatile organic compound (VOC) emissions from soil and litter is relatively limited compared to what we know about VOC emissions from terrestrial plants. With climate change expecting to alter plant community composition, nitrogen (N) deposition rates, mean annual temperatures, and precipitation patterns, it is unknown how production and consumption of VOCs from litter and soil will respond. We spent the last four years quantifying VOC emissions from soil and litter, comparing VOC emissions to CO2 emissions, and identifying the biotic and abiotic controls on emission rates with both lab and field experiments using a proton transfer reaction mass spectrometer (PTR-MS). In all studies, methanol was the dominant VOC flux. VOC emissions were not driven by abiotic processes, as microbial sources accounted for 78% to 99% of the total VOC emissions from decomposing litter. Litter chemistry was correlated with the types of VOCs emitted and the net emissions of carbon as VOCs was found to be up to 88% of that emitted as CO2 suggesting that VOCs likely represent an important component of the carbon cycle in many terrestrial systems. Nitrogen additions drastically reduced VOC emissions from litter to near zero, though it is still not understood whether this was due to an increase in consumption or a decrease in production. Finally, field and lab experiments show that temperature and moisture are both important controls of certain VOC emissions from soils, but that the effects of these factors on VOC emissions are not necessarily equivalent to their effects on CO2 emissions. Together, these series of studies are moving us toward a predictive understanding of VOC emissions from soil and litter with the ultimate goal of incorporating these VOC emissions into global models of terrestrial VOC dynamics.

  17. FERROALLOY PROCESS EMISSIONS MEASUREMENT

    EPA Science Inventory

    The report gives results of sampling and analysis to characterize and quantify particulate, organic, and inorganic chemical emissions in effluents from a totally sealed metallurgical furnace at a ferroalloy plant. Effluents were sampled downstream of a venturi scrubber during sil...

  18. Zero emission targets as long-term global goals for climate protection

    NASA Astrophysics Data System (ADS)

    Rogelj, Joeri; Schaeffer, Michiel; Meinshausen, Malte; Knutti, Reto; Alcamo, Joseph; Riahi, Keywan; Hare, William

    2015-10-01

    Recently, assessments have robustly linked stabilization of global-mean temperature rise to the necessity of limiting the total amount of emitted carbon-dioxide (CO2). Halting global warming thus requires virtually zero annual CO2 emissions at some point. Policymakers have now incorporated this concept in the negotiating text for a new global climate agreement, but confusion remains about concepts like carbon neutrality, climate neutrality, full decarbonization, and net zero carbon or net zero greenhouse gas (GHG) emissions. Here we clarify these concepts, discuss their appropriateness to serve as a long-term global benchmark for achieving temperature targets, and provide a detailed quantification. We find that with current pledges and for a likely (>66%) chance of staying below 2 °C, the scenario literature suggests net zero CO2 emissions between 2060 and 2070, with net negative CO2 emissions thereafter. Because of residual non-CO2 emissions, net zero is always reached later for total GHG emissions than for CO2. Net zero emissions targets are a useful focal point for policy, linking a global temperature target and socio-economic pathways to a necessary long-term limit on cumulative CO2 emissions.

  19. Updated emission inventories for speciated atmospheric mercury from anthropogenic sources in China.

    PubMed

    Zhang, Lei; Wang, Shuxiao; Wang, Long; Wu, Ye; Duan, Lei; Wu, Qingru; Wang, Fengyang; Yang, Mei; Yang, Hai; Hao, Jiming; Liu, Xiang

    2015-03-01

    China is the largest contributor to global atmospheric mercury (Hg), and accurate emission inventories in China are needed to reduce large gaps existing in global Hg mass balance estimates and assess Hg effects on various ecosystems. The China Atmospheric Mercury Emission (CAME) model was developed in this study using probabilistic emission factors generated from abundant on-site measurements and literature data. Using this model, total anthropogenic Hg emissions were estimated to be continuously increasing from 356 t in 2000 to 538 t in 2010 with an average annual increase rate of 4.2%. Industrial coal combustion, coal-fired power plants, nonferrous metal smelting, and cement production were identified to be the dominant Hg emission sources in China. The ten largest contributing provinces accounted for nearly 60% of the total Hg emissions in 2010. Speciated Hg emission inventory was developed over China with a grid-resolution of 36 × 36 km, providing needed emission fields for Hg transport models. In this new inventory, the sectoral Hg speciation profiles were significantly improved based on the latest data from field measurements and more detailed technology categorization. The overall uncertainties of the newly developed inventory were estimated to be in the range of -20% to +23%. PMID:25655106

  20. Spatial and temporal distribution of onroad CO2 emissions at the Urban spatial scale

    NASA Astrophysics Data System (ADS)

    Song, Y.; Gurney, K. R.; Zhou, Y.; Mendoza, D. L.

    2011-12-01

    The Hestia Project is a multi-disciplinary effort to help better understand the spatial and temporal distribution of fossil fuel carbon dioxide (CO2) emission at urban scale. Onroad transportation is an essential source of CO2 emissions. This study examines two urban domains: Marion County (Indianapolis) and Los Angeles County and explores the methods and results associated with the spatial and temporal distribution of local urban onroad CO2 emissions. We utilize a bottom-up approach and spatially distribute county emissions based on the Annual Average Daily Traffic (AADT) counts provided by local Department of Transportation. The total amount of CO2 emissions is calculated by the National Mobile Inventory Model (NMIM) for Marion County and the EMission FACtors (EMFAC) model for Los Angeles County. The NMIM model provides CO2 emissions based on vehicle miles traveled (VMT) data at the county-level from the national county database (NCD). The EMFAC model provides CO2 emissions for California State based on vehicle activities, including VMT, vehicle population and fuel types. A GIS road atlas is retrieved from the US Census Bureau. Further spatial analysis and integration are performed by GIS software to distribute onroad CO2 emission according to the traffic volume. The temporal allocation of onroad CO2 emission is based on the hourly traffic data obtained from the Metropolitan Planning Orgnizations (MPO) for Marion County and Department of Transportation for Los Angeles County. The annual CO2 emissions are distributed according to each hourly fraction of traffic counts. Due to the fact that ATR stations are unevenly distributed in space, we create Thiessen polygons such that each road segment is linked to the nearest neighboring ATR station. The hourly profile for each individual station is then combined to create a "climatology" of CO2 emissions in time on each road segment. We find that for Marion County in the year 2002, urban interstate and arterial roads have less than 15% of total road length and more than 60% of total CO2 emission. Urban minor arterials and major collectors have 9% of the total road length with 21% of the total CO2 emission. Urban minor collectors and local roads have 63% of the total road length and 16% of the total CO2 emission. The rural roads have 13% of the total road length and less than 4% of the total CO2 emission. The temporal distribution shows that the peak hour of CO2 emission is from 7am to 8am in the morning and 4pm to 5pm in the afternoon. Our study also reveals that further downscaling and refining in both spatial and temporal resolution is required to derive more accurate and precise distribution of onroad CO2 emission.

  1. Assessing the impacts of tillage and fertilization management on nitrous oxide emissions in a cornfield using the DNDC model

    NASA Astrophysics Data System (ADS)

    Deng, Qi; Hui, Dafeng; Wang, Junming; Yu, Chih-Li; Li, Changsheng; Reddy, K. Chandra; Dennis, Sam

    2016-02-01

    Quantification and prediction of N2O emissions from croplands under different agricultural management practices are vital for sustainable agriculture and climate change mitigation. We simulated N2O emissions under tillage and no-tillage,and different nitrogen (N) fertilizer types and application methods (i.e., nitrification inhibitor, chicken manure, and split applications) in a cornfield using the DeNitrification-DeComposition (DNDC) model. The model was parameterized with field experimental data collected in Nashville, Tennessee, under various agricultural management treatments and run for a short term (3 years) and a long term (100 years). Results showed that the DNDC model could adequately simulate N2O emissions as well as soil properties under different agricultural management practices. The modeled emissions of N2O significantly increased by 35% with tillage, and decreased by 24% with the use of nitrification inhibitor, compared with no-tillage and normal N fertilization. Chicken manure amendment and split applications of N fertilizer had minor impact on N2O emission in a short term, but over a long term (100 years) the treatments significantly altered N2O emission (+35%, -10%, respectively). Sensitivity analysis showed that N2O emission was sensitive to mean annual precipitation, mean annual temperature, soil organic carbon, and the amount of total N fertilizer application. Our model results provide valuable information for determining agricultural best management practice to maintain highly productive corn yield while reducing greenhouse gas emissions.

  2. Determining national greenhouse gas emissions from waste-to-energy using the Balance Method.

    PubMed

    Schwarzböck, Therese; Rechberger, Helmut; Cencic, Oliver; Fellner, Johann

    2016-03-01

    Different directives of the European Union require operators of waste-to-energy (WTE) plants to report the amount of electricity that is produced from biomass in the waste feed, as well as the amount of fossil CO2 emissions generated by the combustion of fossil waste materials. This paper describes the application of the Balance Method for determining the overall amount of fossil and thus climate relevant CO2 emissions from waste incineration in Austria. The results of 10 Austrian WTE plants (annual waste throughput of around 2,300 kt) demonstrate large seasonal variations in the specific fossil CO2 emissions of the plants as well as large differences between the facilities (annual means range from 32±2 to 51±3kg CO2,foss/GJ heating value). An overall amount of around 924 kt/yr of fossil CO2 for all 10 WTE plants is determined. In comparison biogenic (climate neutral) CO2 emissions amount to 1,187 kt/yr, which corresponds to 56% of the total CO2 emissions from waste incineration. The total energy input via waste feed to the 10 facilities is about 22,500 TJ/yr, of which around 48% can be assigned to biogenic and thus renewable sources. PMID:26847720

  3. TETE: Total Education in the Total Environment.

    ERIC Educational Resources Information Center

    Eblen, William R.

    The Hudson River Museum's Environmental Arts and Science Division has published this booklet describing their model educational program, "TETE: Total Education in the Total Environment," a multidisciplinary approach to environmental education utilizing existing curricula. For conducting the program model communities strategically located along the…

  4. Annual Energy Review 1999

    SciTech Connect

    Seiferlein, Katherine E.

    2000-07-01

    A generation ago the Ford Foundation convened a group of experts to explore and assess the Nation’s energy future, and published their conclusions in A Time To Choose: America’s Energy Future (Cambridge, MA: Ballinger, 1974). The Energy Policy Project developed scenarios of U.S. potential energy use in 1985 and 2000. Now, with 1985 well behind us and 2000 nearly on the record books, it may be of interest to take a look back to see what actually happened and consider what it means for our future. The study group sketched three primary scenarios with differing assumptions about the growth of energy use. The Historical Growth scenario assumed that U.S. energy consumption would continue to expand by 3.4 percent per year, the average rate from 1950 to 1970. This scenario assumed no intentional efforts to change the pattern of consumption, only efforts to encourage development of our energy supply. The Technical Fix scenario anticipated a “conscious national effort to use energy more efficiently through engineering know-how." The Zero Energy Growth scenario, while not clamping down on the economy or calling for austerity, incorporated the Technical Fix efficiencies plus additional efficiencies. This third path anticipated that economic growth would depend less on energy-intensive industries and more on those that require less energy, i.e., the service sector. In 2000, total energy consumption was projected to be 187 quadrillion British thermal units (Btu) in the Historical Growth case, 124 quadrillion Btu in the Technical Fix case, and 100 quadrillion Btu in the Zero Energy Growth case. The Annual Energy Review 1999 reports a preliminary total consumption for 1999 of 97 quadrillion Btu (see Table 1.1), and the Energy Information Administration’s Short-Term Energy Outlook (April 2000) forecasts total energy consumption of 98 quadrillion Btu in 2000. What energy consumption path did the United States actually travel to get from 1974, when the scenarios were drawn, to the end of the century? What happened to the relationship between growth and energy consumption? How did the fuel mix change over this period? What are the effects of energy usage on our environment? What level of consumption will the United States—and the world—record in the Annual Energy Review 2025? We present this edition of the Annual Energy Review to help investigate these important questions and to stimulate and inform our thinking about what the future holds.

  5. Emission database for global atmospheric research (Edgar).

    PubMed

    Olivier, J G; Bouwman, A F; van der Maas, C W; Berdowski, J J

    1994-05-01

    Atmospheric chemistry and climate modellers require gridded global emissions data as input into their models. To meet this urgent need a global emissions source database called EDGAR is being developed by TNO and RIVM to estimate for 1990, on a regional and on a grid basis, annual emissions of greenhouse gases (CO2, CH4, N2O, CO, NOx, non-methane VOC, SOx), of NH3, and of ozone depleting compounds (halocarbons) from all known sources. The aim is to establish at due levels of spatial, temporal and source aggregation the emissions from both anthropogenic and biogenic sources: a complete set of data required to estimate the total source strength of the various gases with a 1×1 ° resolution (altitude resolution of 1 km) and a temporal resolution of a month, supplemented by diurnal variation, as agreed upon in the Global Emissions Inventory Activity (GEIA) of the International Atmospheric Chemistry Programme (IGAC). In this way EDGAR will meet the requirements of present and future developments in the field of atmospheric modelling. The data comprise demographic data, social and economic factors, land use distributions and emission factors (with due emphasis on the uncertainty). As understanding in this field is still changing, due attention is paid to flexibility regarding the disaggregation of sources, spatial and temporal resolution and species. The objective and methodology chosen for the construction of the database and the structural design of the database system are presented, as well as the type and sources of data and the approach used for data collection. As an example, the construction of the N2O inventory is discussed. PMID:24213893

  6. 40 CFR 61.162 - Emission limits.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... pollution control practice for minimizing emissions of inorganic arsenic to the atmosphere to the maximum... EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS National Emission Standard for Inorganic Arsenic Emissions... total arsenic emissions from the glass melting furnace shall be less than 2.5 Mg (2.7 ton) per year,...

  7. Total Artificial Heart

    MedlinePlus

    ... the NHLBI on Twitter. What Is a Total Artificial Heart? A total artificial heart (TAH) is a ... outside power source. Normal Heart and CardioWest Total Artificial Heart Figure A shows the normal structure and ...

  8. A study on the trends of vehicular emissions in the Beijing-Tianjin-Hebei (BTH) region, China

    NASA Astrophysics Data System (ADS)

    Lang, Jianlei; Cheng, Shuiyuan; Wei, Wei; Zhou, Ying; Wei, Xiao; Chen, Dongsheng

    2012-12-01

    This paper aims to study the vehicular emissions trends in the Beijing-Tianjin-Hebei (BTH) region, located in northern China. The multiyear emission inventories of NOX, CO, VOC and PM10 from road vehicles in the period 1999-2010 were developed by the COPERT IV model. Results show that vehicular emissions of CO and VOC have decreased by annual average change rates (AACR) of -3.1% to -5.2% and -4.4% to -6.9% in the study area, respectively. However, due to the rapid development of freight traffic, emissions of NOX and PM10 have kept increasing in Tianjin and Hebei. Based on the vehicular emission inventories, trends of emission levels for vehicles with different standards, as well as the overall effects of implementing vehicular emission mitigation strategies were assessed. It is suggested that passenger cars (PC) with Euro 0 and Euro I standards, which were at higher emission level in the PC fleet, should be gradually eliminated. Although the increasing rates (IR) of emissions from PC were lower than those of the PC population, the sharp growth of PC population in recent years contributed to a remarkable increase of emissions, weakening the overall mitigation effect. Total vehicle population capacity and other mitigation measures should be studied in China in order to develop new and more effective vehicular emission control strategies.

  9. Annual Energy Review 2006

    SciTech Connect

    Seiferlein, Katherine E.

    2007-06-01

    The Annual Energy Review (AER) is the Energy Information Administration's (EIA) primary report of annual historical energy statistics. For many series, data begin with the year 1949. Included are data on total energy production, consumption, and trade; overviews of petroleum, natural gas, coal, electricity, nuclear energy, renewable energy, international energy, as well as financial and environment indicators; and data unit conversion tables. Publication of this report is required under Public Law 95–91 (Department of Energy Organization Act), Section 205(c), and is in keeping with responsibilities given to the EIA under Section 205(a)(2), which states: “The Administrator shall be responsible for carrying out a central, comprehensive, and unified energy data and information program which will collect, evaluate, assemble, analyze, and disseminate data and information....” The AER is intended for use by Members of Congress, Federal and State agencies, energy analysts, and the general public. EIA welcomes suggestions from readers regarding data series in the AER and in other EIA publications.

  10. Annual Energy Review 2011

    SciTech Connect

    Fichman, Barbara T.

    2012-09-01

    The Annual Energy Review (AER) is the U.S. Energy Information Administration's (EIA) primary report of annual historical energy statistics. For many series, data begin with the year 1949. Included are statistics on total energy production, consumption, trade, and energy prices; overviews of petroleum, natural gas, coal, electricity, nuclear energy, and renewable energy; financial and environment indicators; and data unit conversions. Publication of this report is required under Public Law 95–91 (Department of Energy Organization Act), Section 205(c), and is in keeping with responsibilities given to the EIA under Section 205(a)(2), which states: “The Administrator shall be responsible for carrying out a central, comprehensive, and unified energy data and information program which will collect, evaluate, assemble, analyze, and disseminate data and information....” The AER is intended for use by Members of Congress, Federal and State agencies, energy analysts, and the general public. EIA welcomes suggestions from readers regarding the content of the AER and other EIA publications.

  11. Annual Energy Review 2009

    SciTech Connect

    Fichman, Barbara T.

    2010-08-01

    The Annual Energy Review (AER) is the U.S. Energy Information Administration's (EIA) primary report of annual historical energy statistics. For many series, data begin with the year 1949. Included are statistics on total energy production, consumption, trade, and energy prices; overviews of petroleum, natural gas, coal, electricity, nuclear energy, renewable energy, and international energy; financial and environment indicators; and data unit conversions. Publication of this report is required under Public Law 95–91 (Department of Energy Organization Act), Section 205(c), and is in keeping with responsibilities given to the EIA under Section 205(a)(2), which states: “The Administrator shall be responsible for carrying out a central, comprehensive, and unified energy data and information program which will collect, evaluate, assemble, analyze, and disseminate data and information....” The AER is intended for use by Members of Congress, Federal and State agencies, energy analysts, and the general public. EIA welcomes suggestions from readers regarding the content of the AER and other EIA publications.

  12. Annual Energy Review 2005

    SciTech Connect

    Seiferlein, Katherine E.

    2006-07-01

    The Annual Energy Review (AER) is the Energy Information Administration's (EIA) primary report of annual historical energy statistics. For many series, data begin with the year 1949. Included are data on total energy production, consumption, and trade; overviews of petroleum, natural gas, coal, electricity, nuclear energy, renewable energy, international energy, as well as financial and environment indicators; and data unit conversion tables. Publication of this report is required under Public Law 95–91 (Department of Energy Organization Act), Section 205(c), and is in keeping with responsibilities given to the EIA under Section 205(a)(2), which states: “The Administrator shall be responsible for carrying out a central, comprehensive, and unified energy data and information program which will collect, evaluate, assemble, analyze, and disseminate data and information....” The AER is intended for use by Members of Congress, Federal and State agencies, energy analysts, and the general public. EIA welcomes suggestions from readers regarding data series in the AER and in other EIA publications.

  13. Annual Energy Review 2004

    SciTech Connect

    Seiferlein, Katherine E.

    2005-08-01

    The Annual Energy Review (AER) is the Energy Information Administration's (EIA) primary report of annual historical energy statistics. For many series, data begin with the year 1949. Included are data on total energy production, consumption, and trade; overviews of petroleum, natural gas, coal, electricity, nuclear energy, renewable energy, international energy, as well as financial and environment indicators; and data unit conversion tables. Publication of this report is required under Public Law 95–91 (Department of Energy Organization Act), Section 205(c), and is in keeping with responsibilities given to the EIA under Section 205(a)(2), which states: “The Administrator shall be responsible for carrying out a central, comprehensive, and unified energy data and information program which will collect, evaluate, assemble, analyze, and disseminate data and information....” The AER is intended for use by Members of Congress, Federal and State agencies energy analysts, and the general public. EIA welcomes suggestions from readers regarding data series in the AER and in other EIA publications.

  14. NO2 emissions from agricultural burning in São Paulo, Brazil.

    PubMed

    Oppenheimer, Clive; Tsanev, Vitchko I; Allen, Andrew G; McGonigle, Andrew J S; Cardoso, Arnaldo A; Wiatr, Antony; Paterlini, Willian; Dias, Cristine de Mello

    2004-09-01

    We report here on the application of a compact ultraviolet spectrometer to measurement of NO2 emissions from sugar cane field burns in São Paulo, Brazil. The time-resolved NO2 emission from a 10 ha plot peaked at about 240 g (NO2) s(-1), and amounted to a total yield of approximately 50 kg of N, or about 0.5 g (N) m(-2). Emission of N as NOx (i.e., NO + NO2) was estimated at 2.5 g (N) m(-2), equivalent to 30% of applied fertilizer nitrogen. The corresponding annual emission of NOx nitrogen from São Paulo State sugar cane burning was >45 Gg N. In contrast to mechanized harvesting, which does not require prior burning of the crop, manual harvesting with burning acts to recycle nitrogen into surface soils and ecosystems. PMID:15461163

  15. Development of an improved inventory of emissions from pleasure craft in California. Final report

    SciTech Connect

    Chinkin, L.

    1995-06-01

    An updated emissions inventory for California pleasure craft covers total organic gases (TOG), Nox, CO, SOx, and particulate matter (PM). A survey of over 10,000 pleasure craft owners from June 1993 to May 1994 ascertained spatial and temporal utilization of pleasure craft and collected updated consumption rates. Annual fuel consumption is estimated for vessels by propulsion/engine combinations by region (Northern, Central, and Southern). From these, regional and county-level emissions are estimated using a model (PCEM) that includes emission estimates from DMV-registered vessels, Coast Guard-documented vessels, and rental vessels. Fuel consumption is multiplied by emission factors for each propulsion/engine type and allocated to counties with spatial allocation factors developed from the survey data. Temporal activity profiles are derived from the survey data.

  16. Estimation of nitrous oxide emissions from US grasslands

    SciTech Connect

    Mummey, D.L.; Smith, J.L.; Bluhm, G.

    2000-02-01

    Nitrous oxide (N{sub 2}O) emissions from temperate grasslands are poorly quantified and may be an important part of the atmospheric N{sub 2}O budget. In this study N{sub 2}O emissions were simulated for 1,052 grassland sites in the US using the NGAS model of Parton and others (1996) coupled with an organic matter decomposition model. N{sub 2}O flux was calculated for each site using soil and land use data obtained from the National Resource Inventory (NRI) database and weather data obtained from NASA. The estimates were regionalized based upon temperature and moisture isotherms. Annual N{sub 2}O emissions for each region were based on the grassland area of each region and the mean estimated annual N{sub 2}O flux from NRI grassland sites in the region. The regional fluxes ranged from 0.18 to 1.02 kg N{sub 2}O N/ha/yr with the mean flux for all regions being 0.29 kg N{sub 2}O N/ha/yr. Even though fluxes from the western regions were relatively low, these regions made the largest contribution to total emissions due to their large grassland area. Total US grassland N{sub 2}O emissions were estimated to be about 67 Gg N{sub 2}O N/yr. Emissions from the Great Plains states, which contain the largest expanse of natural grassland in the US, were estimated to average 0.24 kg N{sub 2}O N/ha/yr. Using the annual flux estimate for the temperate Great Plains, the authors estimate that temperate grasslands worldwide may potentially produce 0.27 Tg N{sub 2}O N/yr. Even though the estimate for global temperate grassland N{sub 2}O emissions is less than published estimates for other major temperate grasslands are a significant part of both United States and global atmospheric N{sub 2}O budgets. This study demonstrates the utility of models for regional N{sub 2}O budgets. This study demonstrates the utility of models for regional N{sub 2}O flux estimation although additional data from carefully designed field studies is needed to further validate model results.

  17. Wastewater treatment process impact on energy savings and greenhouse gas emissions.

    PubMed

    Mamais, D; Noutsopoulos, C; Dimopoulou, A; Stasinakis, A; Lekkas, T D

    2015-01-01

    The objective of this research was to assess the energy consumption of wastewater treatment plants (WWTPs), to apply a mathematical model to evaluate their carbon footprint, and to propose energy saving strategies that can be implemented to reduce both energy consumption and greenhouse gas (GHG) emissions in Greece. The survey was focused on 10 WWTPs in Greece with a treatment capacity ranging from 10,000 to 4,000,000 population equivalents (PE). Based on the results, annual specific energy consumption ranged from 15 to 86 kWh/PE. The highest energy consumer in all the WWTPs was aeration, accounting for 40-75% of total energy requirements. The annual GHG emissions varied significantly according to the treatment schemes employed and ranged between 61 and 161 kgCO₂e/PE. The highest values of CO₂emissions were obtained in extended aeration systems and the lowest in conventional activated sludge systems. Key strategies that the wastewater industry could adopt to mitigate GHG emissions are identified and discussed. A case study is presented to demonstrate potential strategies for energy savings and GHG emission reduction. Given the results, it is postulated that the reduction of dissolved oxygen (DO) set points and sludge retention time can provide significant energy savings and decrease GHG emissions. PMID:25633956

  18. Emissions from International Shipping in the Arctic

    NASA Astrophysics Data System (ADS)

    Corbett, J. J.; Winebrake, J. J.; Gold, M.; Harder, S.

    2008-12-01

    Studies assessing the potential impacts of international shipping on climate and air pollution demonstrate that ships contribute significantly to global climate change and health impacts through emission of GHGs and raised the potential for disproportionate impacts from shipping in the Arctic region. We present an activity- based model inventory of emissions of CO2, BC, NOx, SOx, PM, and CO for shipping in the Arctic. We estimate emissions for a particular "vessel-trip" or "voyage" based on Arctic shipping data collected by the Arctic Marine Shipping Assessment for 2004. The detailed voyage data provided for our inventory effort included some 3800 ship trips, represent some 2.6 million km of ship voyages (range 2.0 to 3.9 million km, or 1.1 to 2.1 million nautical miles), and nearly 15,000 voyage days for 2004; this is equivalent to less than 500 transoceanic voyages, compared to many tens of thousands transoceanic voyages per year to major ports around the world. In 2004, the top five vessel types, bulk carrier, general cargo, fishing, government vessels, and containerships, account for nearly 80 percent of total emissions. Preliminary results show CO2 emissions from shipping in the Arctic to be approximately 2.3 Tg CO2 per yr. Given that total CO2 emissions from international shipping globally are about 1000 Tg CO2 per yr, Arctic contributions would amount to less than 0.25 percent of total ship emissions. Relative to total CO2 emissions from all sources, the contributions of Arctic shipping are on the order of one-hundredth of one percent (0.006-0.008 percent). BC emissions from Arctic shipping, on a mass basis alone (estimated here to be ~600 tonnes /year), may have limited independent impact on global climate change compared to other sources, but could have significant regional impacts. More concerning may be micro-scale emissions (e.g., at harbor or in port) which could affect local air pollution or ecosystems, depending on regional conditions. Pollutants with more regional impact include NOx, SOx, CO, and PM. For these pollutants Arctic shipping emissions are small contributors to global inventories on a mass basis. For example, Arctic shipping accounts for about 62,400 tonnes per year of NOX pollution in the Arctic region, about 0.3 percent of 25.6 Tg of NOx (as NO2, or 7.8 Tg as N in 2007) global ship NOx emissions. Future trends toward increased international shipping in the Arctic will increase these numbers proportional to the increased traffic, although future research is needed to determine whether the increased climate-scale impacts would be proportional to Arctic shipping activity. Previous research (Granier et al, GRL 2006) indicated that shipping growth could account for an additional 0.65 to 1.3 million Tg N from Arctic shipping (2.5 Tg to 4.9 Tg NOx as NO2). Using our preliminary inventory results, this corresponds to between 40 and 70 times more Arctic shipping activity in 2050 than in 2004, representing annually compounding growth rates in the range of 8 to 10 percent. We will present our inventory and discuss data quality needs to better reduce the uncertainty in Arctic shipping inventories.

  19. Estimates of emissions from open biomass burning in Tropical Asia during 2000-2007

    NASA Astrophysics Data System (ADS)

    Chang, D.

    2009-04-01

    Biomass burning in tropical Asia emits large amounts of trace gases and particulate matters to atmosphere, which have significant influence in climate change and atmospheric chemistry. Emissions from open biomass burning in tropical Asia are estimated during seven fire years 2000-2006 (i.e., April 1st 2000-March 31st 2007), using newly released L3JRC burned area product and MODIS burned area product (MCD45A1). Over seven fire years, both burned areas and fire emissions showed clearly spatial and inter-annual variations. The L3JRC burned areas ranged from 31.3×103 km2 for fire year 2005 to 57.5×103 km2 for 2000, while the MODIS burned areas ranged from 64.9×103 km2 for fire year 2002 to 127.0×103 km2 for 2004. We compared the total burned areas and forest burned areas derived from the two separate products with publication data for several typical countries and found that the L3JRC results were comparable to previous studies and the MODIS results showed significant overestimation. The annual average L3JRC-based emissions were 29915, 1948, 90, 30, 12, 105, and 871 Gg yr-1 for CO2, CO, CH4, NOx, BC, OC, and PM2.5 respectively, while MODIS-based emissions were 86740, 5222, 230, 83, 33, 296, and 2188 Gg yr-1, 60.2%-65.5% higher than L3JRC. Forest fires were the largest contributor to fire emissions, though burned area within forest biomes only constituted a minority of total burned area. Fire emissions were mainly concentrated in Myanmar, Cambodia and India. Furthermore, the seasonal distribution of fire emissions was in good agreement with that of total burned areas.

  20. 33rd Annual Official Education Construction Report

    ERIC Educational Resources Information Center

    Agron, Joe

    2007-01-01

    Construction spending by education institutions topped $36 billion in 2006. While strong by historical standards, it represents the third consecutive year that total spending on construction dropped from the year before. According to the "American School & University" 33rd annual Official Education Construction Report, total spending on new,…

  1. Variation Trend and Driving Factors of Greenhouse Gas Emissions from Chinese Magnesium Production.

    PubMed

    Gao, Feng; Liu, Yu; Nie, Zuo-Ren; Gong, Xianzheng; Wang, Zhihong

    2015-11-01

    As the largest magnesium producer in the world, China is facing a great challenge of greenhouse gas (GHG) emissions reduction. In this paper, the variation trend and driving factors of GHG emissions from Chinese magnesium production were evaluated and the measures of technology and policy for effectively mitigating GHG emissions were provided. First, the energy-related and process-oriented GHG inventory is compiled for magnesium production in China. Then, the driving forces for the changes of the energy-related emission were analyzed by the method of Logarithmic Mean Divisia Index (LMDI) decomposition. Results demonstrated that Chinese magnesium output from 2003 to 2013 increased by 125%, whereas GHG emissions only increased by 16%. The emissions caused by the fuels consumption decline most significantly (from 28.4 to 6.6 t CO2eq/t Mg) among all the emission sources. The energy intensity and the energy structure were the main offsetting factors for the increase of GHG emissions, while the scale of production and the international market demand were the main contributors for the total increase. Considering the improvement of technology application and more stringent policy measures, the annual GHG emissions from Chinese primary magnesium production will be controlled within 22 million tons by 2020. PMID:26458120

  2. Testing and modeling the influence of reclamation and control methods for reducing nonpoint mercury emissions associated with industrial open pit gold mines.

    PubMed

    Miller, Matthieu B; Gustin, Mae S

    2013-06-01

    Industrial gold mining is a significant source of mercury (Hg) emission to the atmosphere. To investigate ways to reduce these emissions, reclamation and dust and mercury control methods used at open pit gold mining operations in Nevada were studied in a laboratory setting. Using this information along with field data, and building off previous work, total annual Hg emissions were estimated for two active gold mines in northern Nevada. Results showed that capping mining waste materials with a low-Hg substrate can reduce Hg emissions from 50 to nearly 100%. The spraying of typical dust control solutions often results in higher Hg emissions, especially as materials dry after application. The concentrated application of a dithiocarbamate Hg control reagent appears to reduce Hg emissions, but further testing mimicking the actual distribution of this chemical within an active leach solution is needed to make a more definitive assessment. PMID:23858994

  3. 21 CFR 1002.13 - Annual reports.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... the due date of the report. (c) New models of a model family that do not involve changes in radiation emission or requirements of a performance standard do not require supplemental reports prior to introduction into commerce. These model numbers should be reported in quarterly updates to the annual report....

  4. Global production and emissions of bromochlorodifluoromethane and bromotrifluoromethane (halons 1211 and 1301)

    NASA Astrophysics Data System (ADS)

    McCulloch, Archie

    Data for the global production of Halons 1211 and 1301 have been assembled from audieted values submitted by procedures within OECD (Organisation for Economic Cooperation and Development, comprising Australia, Canada, Japan, New Zealand, U.S.A. and European countries, excluding those in the former Eastern bloc) and from estimates of production in U.S.S.R. and China. Aggregate values for production are accurate to within 3% for Halon 1211 and 2% for Halon 1301. Annual emissions of these Halons have been calculated from the production figures and industrial estimates of the annual percentages released. The totals of these emissions up to and including 1990 are 112,946 tonnes of Halon 1211 and 48,377 tonnes of Halon 1301; values which, after discounting for the atmosphericlifetimes of these compounds, are generally consistent with measured atmospheric concentrations.

  5. Comparison of two U.S. power-plant carbon dioxide emissions data sets

    USGS Publications Warehouse

    Ackerman, K.V.; Sundquist, E.T.

    2008-01-01

    Estimates of fossil-fuel CO2 emissions are needed to address a variety of climate-change mitigation concerns over a broad range of spatial and temporal scales. We compared two data sets that report power-plant CO 2 emissions in the conterminous U.S. for 2004, the most recent year reported in both data sets. The data sets were obtained from the Department of Energy's Energy Information Administration (EIA) and the Environmental Protection Agency's eGRID database. Conterminous U.S. total emissions computed from the data sets differed by 3.5% for total plant emissions (electricity plus useful thermal output) and 2.3% for electricity generation only. These differences are well within previous estimates of uncertainty in annual U.S. fossil-fuel emissions. However, the corresponding average absolute differences between estimates of emissions from individual power plants were much larger, 16.9% and 25.3%, respectively. By statistical analysis, we identified several potential sources of differences between EIA and eGRID estimates for individual plants. Estimates that are based partly or entirely on monitoring of stack gases (reported by eGRID only) differed significantly from estimates based on fuel consumption (as reported by EIA). Differences in accounting methods appear to explain differences in estimates for emissions from electricity generation from combined heat and power plants, and for total and electricity generation emissions from plants that burn nonconventional fuels (e.g., biomass). Our analysis suggests the need for care in utilizing emissions data from individual power plants, and the need for transparency in documenting the accounting and monitoring methods used to estimate emissions.

  6. Measurement of emission fluxes from Technical Area 54, Area G and L. Final report

    SciTech Connect

    Eklund, B.

    1995-03-15

    The emission flux (mass/time-area) of tritiated water from TA-54 was measured to support the characterization of radioactive air emissions from waste sites for the Radioactive Air Emissions Management (RAEM) program and for the Area G Performance Assessment. Measurements were made at over 180 locations during the summers of 1993 and 1994, including randomly selected locations across Area G, three suspected areas of contamination at Area G, and the property surrounding TA-54. The emission fluxes of radon were measured at six locations and volatile organic compounds (VOCs) at 30 locations. Monitoring was performed at each location over a several-hour period using the U.S. EPA flux chamber approach. Separate samples for tritiated water, radon, and VOCs were collected and analyzed in off-site laboratories. The measured tritiated water emission fluxes varied over several orders of magnitude, from background levels of about 3 pCi/m{sup 2}-min to 9.69 x 10{sup 6} pCi/m{sup 2}-min near a disposal shaft. Low levels of tritiated water were found to have migrated into Pajarito Canyon, directly south of Area G. The tritium flux data were used to generate an estimated annual emission rate of 14 Curies/yr for all of Area G, with the majority of this activity being emitted from relatively small areas adjacent to several disposal shafts. The estimated total annual release is less than 1% of the total tritium release from all LANL in 1992 and results in a negligible off-site dose. Based on the limited data available, the average emission flux of radon from Area G is estimated to be 8.1 pCi/m{sup 2}-min. The measured emission fluxes of VOCs were < 100 {mu}g/m{sup 2}-min, which is small compared with fluxes typically measured at hazardous waste landfills. The air quality impacts of these releases were evaluated in a separate report.

  7. Emissions of volatile fatty acids from feed at dairy facilities

    NASA Astrophysics Data System (ADS)

    Alanis, Phillip; Ashkan, Shawn; Krauter, Charles; Campbell, Sean; Hasson, Alam S.

    2010-12-01

    Recent studies suggest that dairy operations may be a major source of non-methane volatile organic compounds in dairy-intensive regions such as Central California, with short chain carboxylic acids (volatile fatty acids or VFAs) as the major components. Emissions of four VFAs (acetic acid, propanoic acid, butanoic acid and hexanoic acid) were measured from two feed sources (silage and total mixed rations (TMR)) at six Central California Dairies over a fifteen-month period. Measurements were made using a combination of flux chambers, solid phase micro-extraction fibers coupled to gas chromatography mass spectrometry (SPME/GC-MS) and infra-red photoaccoustic detection (IR-PAD for acetic acid only). The relationship between acetic acid emissions, source surface temperature and four sample composition factors (acetic acid content, ammonia-nitrogen content, water content and pH) was also investigated. As observed previously, acetic acid dominates the VFA emissions. Fluxes measured by IR-PAD were systematically lower than SPME/GC-MS measurements by a factor of two. High signals in field blanks prevented emissions from animal waste sources (flush lane, bedding, open lot) from being quantified. Acetic acid emissions from feed sources are positively correlated with surface temperature and acetic acid content. The measurements were used to derive a relationship between surface temperature, acetic acid content and the acetic acid flux. The equation derived from SPME/GC-MS measurements predicts estimated annual average acetic acid emissions of (0.7 + 1/-0.4) g m -2 h -1 from silage and (0.2 + 0.3/-0.1) g m -2 h -1 from TMR using annually averaged acetic acid content and meteorological data. However, during the summer months, fluxes may be several times higher than these values.

  8. 40 CFR 98.223 - Calculating GHG emissions.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... (CONTINUED) MANDATORY GREENHOUSE GAS REPORTING Nitric Acid Production § 98.223 Calculating GHG emissions. (a) You must determine annual N2O process emissions from each nitric acid train according to paragraphs (a...) You must conduct an annual performance test for each nitric acid train according to paragraphs...

  9. 40 CFR 98.223 - Calculating GHG emissions.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... (CONTINUED) MANDATORY GREENHOUSE GAS REPORTING Nitric Acid Production § 98.223 Calculating GHG emissions. (a) You must determine annual N2O process emissions from each nitric acid train according to paragraphs (a...) You must conduct an annual performance test for each nitric acid train according to paragraphs...

  10. 40 CFR 98.223 - Calculating GHG emissions.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... (CONTINUED) MANDATORY GREENHOUSE GAS REPORTING Nitric Acid Production § 98.223 Calculating GHG emissions. (a) You must determine annual N2O process emissions from each nitric acid train according to paragraphs (a...) You must conduct an annual performance test for each nitric acid train according to paragraphs...

  11. 40 CFR 98.223 - Calculating GHG emissions.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... (CONTINUED) MANDATORY GREENHOUSE GAS REPORTING Nitric Acid Production § 98.223 Calculating GHG emissions. (a) You must determine annual N2O process emissions from each nitric acid train according to paragraphs (a...) You must conduct an annual performance test for each nitric acid train according to paragraphs...

  12. 1992 Carbon emissions data

    SciTech Connect

    1995-12-31

    This article reports on the global total of carbon dioxide emissions from fossil-fuel burning and cement manufacture in 1992. The total estimate of 6097 million metric tons of carbon is essentially the same for 1990 and down slightly from 1991, but 7 of 9 geographical regions had increases.

  13. Nitrous oxide emission hotspots from organic soils in Europe

    NASA Astrophysics Data System (ADS)

    Leppelt, T.; Dechow, R.; Gebbert, S.; Freibauer, A.; Lohila, A.; Augustin, J.; Drösler, M.; Fiedler, S.; Glatzel, S.; Höper, H.; Järveoja, J.; Lærke, P. E.; Maljanen, M.; Mander, Ü.; Mäkiranta, P.; Minkkinen, K.; Ojanen, P.; Regina, K.; Strömgren, M.

    2014-06-01

    Organic soils are a main source of direct nitrous oxide (N2O) emissions, an important greenhouse gas (GHG). Observed N2O emissions from organic soils are highly variable in space and time which causes high uncertainties in national emission inventories. Those uncertainties could be reduced when relating the upscaling process to a priori identified key drivers by using available N2O observations from plot scale in empirical approaches. We used the empirical fuzzy modelling approach MODE to identify main drivers for N2O and utilize them to predict the spatial emission pattern of European organic soils. We conducted a meta study with a total amount of 659 annual N2O measurements which was used to derive separate models for different land use types. We applied our models to available, spatial explicit input driver maps to upscale N2O emissions on European level and compared the inventory with recently published IPCC emission factors. The final statistical models explained up to 60% of the N2O variance. Our study results showed that cropland and grasslands emitted the highest N2O fluxes 0.98 ± 1.08 and 0.58 ± 1.03 g N2O-N m-2 a-1, respectively. High fluxes from cropland sites were mainly controlled by low soil pH-value and deep drained groundwater tables. Grassland hotspot emissions were strongly related to high amount of N-fertilizer inputs and warmer winter temperatures. In contrast N2O fluxes from natural peatlands were predominantly low (0.07±0.27 g N2O-N m-2 a-1) and we found no relationship with the tested drivers. The total inventory for direct N2O emissions from organic soils in Europe amount up to 149.5 Gg N2O-N a-1, which included also fluxes from forest and peat extraction sites and exceeds the inventory calculated by IPCC emission factors of 87.4 Gg N2O-N a-1. N2O emissions from organic soils represent up to 13% of total European N2O emissions reported in the European Union (EU) greenhouse gas inventory of 2011 from only 7% of the EU area. Thereby the model demonstrated that with up to 85% the major part of the inventory is induced by anthropogenic management, which shows the significant reduction potential by rewetting and extensivation of agricultural used peat soils.

  14. Top-down analysis of the elemental carbon emissions inventory in the United States by inverse modeling using Community Multiscale Air Quality model with decoupled direct method (CMAQ-DDM)

    NASA Astrophysics Data System (ADS)

    Hu, Yongtao; Odman, M. Talat; Russell, Armistead G.

    2009-12-01

    A Community Multiscale Air Quality (CMAQ) model based inverse method is used for calibrating the 2004 elemental carbon (EC) emissions in the continental United States. We convert the Thermal Optical Transmittance (TOT) EC measurements to the Thermal Optical Reflectance (TOR) equivalents to fully utilize available observational networks. The reestimate of the total emissions is 0.40 Tg yr-1, about 13% higher than the a priori. The posterior CMAQ simulation driven by the adjusted emissions had an ˜10% reduction in annual average fractional error based on 24 h EC observations. Comparison of simulated EC concentrations to hourly aethalometer black carbon (BC) measurements improved as well. Also, using the EC scaling factors to adjust the primary particulate organic matter (OM) emissions improved performance for OM simulation. Results show that splitting sources further spatially and category-wise increases the flexibility of adjusting emissions according to the spatial variability of the emissions strength and hence makes a better reestimate of emissions.

  15. Side-by-side comparison of field monitoring methods for hot bitumen emission exposures: the German IFA Method 6305, U.S. NIOSH Method 5042, and the Total Organic Matter Method.

    PubMed

    Kriech, Anthony J; Emmel, Christoph; Osborn, Linda V; Breuer, Dietmar; Redman, Adam P; Hoeber, Dieter; Bochmann, Frank; Ruehl, Reinhold

    2010-12-01

    Field studies were conducted at paving and roofing sites to compare the German Institute for Occupational Safety and Health of the German Social Accident Insurance (IFA) Fourier transform infrared spectroscopy method 6305 with the National Institute for Occupational Science and Health (NIOSH) benzene soluble fraction method 5042 plus total organic matter. Sampling using both methods was performed in multiple bitumen-related workplace environments. To provide comparable data all samplings were performed in parallel, and the analytical data were related to the same representative bitumen condensate standard. An outline of the differences between the sampling and analytical methods is provided along with comparative data obtained from these site investigations. A total of 55 bitumen paving sampler pairs were reported and statistical comparisons made using the 35 pairs of detectable data. First, the German inhalable aerosol data and the NIOSH benzene soluble fraction (BSF) method showed a correlation coefficient of R²= 0.88 (y((BSF))= 0.60 x((aerosol))). Second, the aerosol data compared with total particulate matter (TPM) show a R² of 0.83 (y((TPM))= 1.01 x((aerosol))). Finally, total organic matter (TOM) and "aerosol + vapor" data yielded a R² of 0.78 (y((TOM))= 0.44 x((aerosol+vapor))). Twenty-nine pairs of roofing data were also collected; 37% were below the limit of detection. When comparing the TOM data with the aerosol + vapor data, using the 13 of 29 pairs where both samplers showed detectable results, the relationship was y((TOM))= 0.74 x((aerosol+vapor)) (R²= 0.91). The slopes within these equations provide predictive factors between these sampling and analysis methods; intended for use with large sets of data, they are not applicable to single point measurements. PMID:21058156

  16. Fertiliser induced nitrous oxide emissions during energy crop cultivation on loamy sand soils

    NASA Astrophysics Data System (ADS)

    Hellebrand, Hans J.; Scholz, Volkhard; Kern, Jürgen

    Nitrous oxide (N 2O) fluxes from a loamy sand soil have been collected at an experimental field since 1999. To study the nitrogen (N) fertiliser induced emissions, annual crops and perennial plants received three different levels of N fertilisation: 0, 75, and 150 kg N ha -1. N 2O was measured by gas chromatography and closed chamber technique. Water content of the soil was determined gravimetrically and the soil content of mineral N by ion chromatography. The N 2O fluxes were below 30 μg N 2O m -2 h -1 during the winter season and varied from 10 to more than 1000 μg N 2O m -2 h -1 in the course of the vegetation season. N 2O emissions after N fertilisation were assigned to fertiliser induced emissions. High N 2O emissions at the end of the vegetation period are the result of increased mineralisation of soil organic matter. N 2O emissions from freeze-thaw cycles gave only a small contribution to the total annual N 2O emission budget from all blocks studied. Since the mean soil moisture content is very low (10%) and the water-filled pore space (WFPS) correlates negatively with N 2O emissions, nitrification is considered the main source for N 2O emissions. Evaluation of the data regarding dependence on fertilisation level indicates that N 2O fluxes are positively correlated to soil NO 3-N content. The N 2O fluxes from annual crop plots are higher than those from plots with perennial plants (grass, willow, poplar). The mean N 2O-N emission factor for fertiliser induced emissions from tilled soil is 1.0% in contrast to that of non-tilled soil with 0.7%. The mean fertiliser induced N 2O-N emissions, averaged over all crops and the total period of nine years, are in the range of 0.8 ± 0.2% of the N fertiliser applied.

  17. 40 CFR 51.122 - Emissions reporting requirements for SIP revisions relating to budgets for NOX emissions.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... emissions. (f) Reporting schedules. (1) Data collection is to begin during the ozone season 1 year prior to... Submitting Reports Data collection year Type ofreport required 2005 Triennial. 2006 Annual. 2007 Annual. 2008... OF IMPLEMENTATION PLANS Control Strategy § 51.122 Emissions reporting requirements for SIP...

  18. 40 CFR 51.122 - Emissions reporting requirements for SIP revisions relating to budgets for NOX emissions.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... emissions. (f) Reporting schedules. (1) Data collection is to begin during the ozone season 1 year prior to... Submitting Reports Data collection year Type ofreport required 2005 Triennial. 2006 Annual. 2007 Annual. 2008... OF IMPLEMENTATION PLANS Control Strategy § 51.122 Emissions reporting requirements for SIP...

  19. 40 CFR 51.122 - Emissions reporting requirements for SIP revisions relating to budgets for NOX emissions.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... emissions. (f) Reporting schedules. (1) Data collection is to begin during the ozone season 1 year prior to... Submitting Reports Data collection year Type ofreport required 2005 Triennial. 2006 Annual. 2007 Annual. 2008... OF IMPLEMENTATION PLANS Control Strategy § 51.122 Emissions reporting requirements for SIP...

  20. Investigation of VOC emissions from indoor and outdoor painting processes in shipyards

    NASA Astrophysics Data System (ADS)

    Celebi, Ugur Bugra; Vardar, Nurten

    Volatile organic compounds (VOCs) from painting solvents are one of the most important sources of pollutant outputs for the shipbuilding and ship repair industry. Two ships of equal tonnage with the same painted area as each other, which were built in Turkish shipyards, are compared in terms of VOCs produced during painting and coating. Total area of all painted surfaces and total paint consumption of a 3500 deadweight tonne (DWT) oil/chemical tanker and a general cargo ship are calculated. An improved model for calculating the surface emissions of VOCs from painting and coating processes is utilized. Material balance emission estimation approach is employed to calculate the amount of VOCs, since it is used most often where a relatively large amount of material is emitted during use, and/or all air emissions are uncaptured. For both ships calculated VOCs are presented in figures. For the years 2005 and 2006 the total deadweight tonnage of ships delivered in Tuzla region, where 42 shipyards are located, is known. Therefore, a linear estimation is made to guess the total annual VOC emissions caused by painting operations. Finally, this information is used to project the total amount of VOCs emitted to the atmosphere for the year 2010.

  1. Abatement of methane emissions from landfills -- the German way

    SciTech Connect

    Angerer, G.; Kalb, H.

    1996-12-31

    Landfills are a major source of methane. Methane is generated by biological degradation of native organic matter under anaerobic conditions. In Germany one quarter to one third of the total methane emissions into the air originate from landfills for municipal wastes. These emissions amounts to 1.2--1.9 million metric tons annually. Landfills represent the second most important methane source. For stock farming the technical opportunities to reduce methane emissions are limited. Therefore, environmental policy aiming to abate methane emissions focuses on waste management. In Germany the most effective policy instrument for this task is the Third Administrative Provision to the waste framework law. This provision came into operation in 1993 and requires that waste disposed in landfills must be inert. Beginning in the year 2005 the total organic carbon (TOC) content of the waste will be limited to 1--3%. This limit requires a pretreatment of municipal waste, and among the currently available technology options only an incineration is able to fulfill the stipulated criteria. Methane abatement will be further regulated by the new waste law, Cycle Economy and Waste Law.

  2. Relative contributions of soil, foliar, and woody tissue respiration to total ecosystem respiration in four pine forests of different ages

    NASA Astrophysics Data System (ADS)

    Khomik, Myroslava; Arain, M. Altaf; Brodeur, Jason J.; Peichl, Matthias; Restrepo-Coupé, Natalia; McLaren, Joshua D.

    2010-09-01

    Carbon dioxide (CO2) emissions from soil, foliage, and live woody tissue were measured throughout the year in afforested, white pine (Pinus strobus L.) stands (67, 32, 17, and 4 years old as of 2006), growing in a northern temperate climate. The data were used to estimate annual ecosystem respiration (Re) and its component fluxes, including soil, foliar, and woody tissue respiration; to investigate major environmental factors causing intersite and temporal variability in the observed fluxes; and to compare chamber-based Re estimates with eddy covariance-based estimates. While temperature was the dominant driving factor of temporal variability in component fluxes, intersite variability in CO2 emissions was attributed to differences in stand physiological characteristics, such as the presence of the LFH soil horizon, its carbon-to-nitrogen ratio, and the amount of canopy cover. Additional factors that contributed to flux variability included the frequency of precipitation events, vapor pressure deficit and stem diameter, depending on the component considered. Estimated annual chamber-based totals of Re across the four stands were 1526 ± 137, 1278 ± 137, 1985 ± 293, and 773 ± 46 g C m-2 yr-1 for the 67-, 32-, 17-, and 4-year-old stands, respectively. Soil respiration dominated emissions at the 4-year-old stand, while foliar respiration dominated emissions at the 17-year-old stand. In contrast, at the two oldest stands, soil and foliar respirations were comparable. Soil respiration accounted for 44%, 44%, 26%, and 70% of annual Re, across the 67-, 32-, 17-, and 4-year-old stands, while foliar respiration accounted for 48%, 41%, 60%, and 30% of annual Re, across the respective sites. Wood respiration was the smallest component of annual Re across the stands (8%, 15%, 14%, and 0.1%, respectively). The chamber-based Re values were higher than tower-based eddy covariance Re estimates, on average by 18%, 70%, 18%, and 36% at the 67-, 32-, 17-, and 4-year-old stands, respectively. This study contributes to our general understanding of the age-related effects and the role of climate on carbon emissions from various components of afforested ecosystems. Our results suggest that foliar respiration could be comparable to or higher than soil respiration in its contribution to Re in young to mature, planted or afforested, ecosystems. They also suggest that site quality and stand age are important factors to be considered in future studies of carbon dynamics of afforested stands.

  3. A high-resolution and multi-year emissions inventory for biomass burning in Southeast Asia during 2001-2010

    NASA Astrophysics Data System (ADS)

    Shi, Yusheng; Yamaguchi, Yasushi

    2014-12-01

    Biomass burning (BB) emissions from forest fires, agricultural waste burning, and peatland combustion contain large amounts of greenhouse gases (e.g., CO2, CH4, and N2O), which significantly impact ecosystem productivity, global atmospheric chemistry, and climate change. With the help of recently released satellite products, biomass density based on satellite and observation data, and spatiotemporal variable combustion factors, this study developed a new high-resolution and multi-year emissions inventory for BB in Southeast Asia (SEA) during 2001-2010. The 1-km grid was effective for quantifying emissions from small-sized fires that were frequently misinterpreted by coarse grid data due to their large smoothed pixels. The average annual BB emissions in SEA during 2001-2010 were 277 Gg SO2, 1125 Gg NOx, 55,388 Gg CO, 3831 Gg NMVOC, 553 Gg NH3, 324 Gg BC, 2406 Gg OC, 3832 Gg CH4, 817,809 Gg CO2, and 99 Gg N2O. Emissions were high in western Myanmar, Northern Thailand, eastern Cambodia, northern Laos, and South Sumatra and South Kalimantan of Indonesia. Emissions from forest burning were the dominant contributor to the total emissions among all land types. The spatial pattern of BB emissions was consistent with that of the burned areas. In addition, BB emissions exhibited similar temporal trends from 2001 to 2010, with strong interannual and intraannual variability. Interannual and intraannual emission peaks were seen during 2004, 2007, 2010, and January-March and August-October, respectively.

  4. A new gridded on-road CO2 emissions inventory for the United States, 1980-2011

    NASA Astrophysics Data System (ADS)

    Gately, C.; Hutyra, L.; Sue Wing, I.

    2013-12-01

    On-road transportation is responsible for 28% of all U.S. fossil fuel CO2 emissions. However, mapping vehicle emissions at regional scales is challenging due to data limitations. Existing emission inventories have used spatial proxies such as population and road density to downscale national or state level data, which may introduce errors where the proxy variables and actual emissions are weakly correlated. We have developed a national on-road emissions inventory product based on roadway-level traffic data obtained from the Highway Performance Monitoring System. We produce annual estimates of on-road CO2 emissions at a 1km spatial resolution for the contiguous United States for the years 1980 through 2011. For the year 2011 we also produce an hourly emissions product at the 1km scale using hourly traffic volumes from hundreds of automated traffic counters across the country. National on-road emissions rose at roughly 2% per year from 1980 to 2006, with emissions peaking at 1.71 Tg CO2 in 2007. However, while national emissions have declined 6% since the peak, we observe considerable regional variation in emissions trends post-2007. While many states show stable or declining on-road emissions, several states and metropolitan areas in the Midwest, mountain west and south had emissions increases of 3-10% from 2008 to 2011. Our emissions estimates are consistent with state-reported totals of gasoline and diesel fuel consumption. This is in contrast to on-road CO2 emissions estimated by the Emissions Database of Global Atmospheric Research (EDGAR), which we show to be inconsistent in matching on-road emissions to published fuel consumption at the scale of U.S. states, due to the non-linear relationships between emissions and EDGAR's chosen spatial proxies at these scales. Since our emissions estimates were generated independent of population density and other demographic data, we were able to conduct a panel regression analysis to estimate the relationship between these variables and on-road CO2 at various spatial scales. In the case of Massachusetts we find a non-linear relationship between emissions and population density indicating that increasing density resulted in increased emissions when density is less than 2000 persons-km-2. These results highlight the value of using an emissions inventory with high spatial and temporal resolution. At coarser spatial scales, much of the variation in population density and on-road emissions between towns is lost due to aggregation. The high spatial resolution and broad temporal scope of our CO2 estimates provides a basis for analyses to support emissions monitoring, verification and mitigation policies at regional, state and local scale.

  5. Annual Check-up

    MedlinePlus

    ... Medical Conditions Nutrition & Fitness Emotional Health Annual Check-Up Posted under Health Guides . Updated 7 January 2015. + ... I get ready for my annual medical check-up? If this is your first visit to your ...

  6. Emissions of mercury and other trace elements from coal-fired power plants in Japan.

    PubMed

    Ito, Shigeo; Yokoyama, Takahisa; Asakura, Kazuo

    2006-09-01

    To evaluate trace element emissions from modern coal-fired power plants into the atmospheric environment in Japan, trace elements in the coal used in electric utility boilers, stack concentrations, emission rates and emission ratios of coal-fired power plants, and proportions of trace elements in coal-fired power plants were studied. The elements were As, B, Be, Cd, Co, Cr, F, Hg, Mn, Ni, Pb, Sb, Se and V, which are designated in the Law of Pollutant Release and Transfer Register. The particulate trace elements were collected in an electrostatic precipitator and a wet desulfurization scrubber. Emissions into the atmosphere were lower than 1% of the quantity in coal, but the volatile trace elements showed somewhat higher emission ratios. For mercury, the mean concentration in coal was 0.045 ppm, the mean emission rate was 4.4 microg/kW h, and the mean emission ratio was 27%, the highest ratio among all elements in this study. The total annual emission of mercury from coal-fired power plants of the electric power industry in Japan was estimated to be 0.63 t/y. On the basis of these data, the atmospheric environment loads from a coal-fired power station were investigated. The calculation of stack gas dispersion showed that maximum annual mean ground level concentrations were in the order of 10(-2) to 10(-5) of the background concentrations, and that the adverse effect of the emissions from the coal-fired power station was small. PMID:16225907

  7. A new European plant-specific emission inventory of biogenic volatile organic compounds for use in atmospheric transport models

    NASA Astrophysics Data System (ADS)

    Karl, M.; Guenther, A.; Köble, R.; Leip, A.; Seufert, G.

    2009-06-01

    We present a new European plant-specific emission inventory for isoprene, monoterpenes, sesquiterpenes and oxygenated VOC (OVOC), on a spatial resolution of 0.089×0.089 degrees, for implementation in atmospheric transport models. The inventory incorporates more accurate data on foliar biomass densities from several litterfall databases that became available in the last years for the main tree species in Europe. A bioclimatic correction factor was introduced to correct the foliar biomass densities of trees and crops for the different plant growth conditions that can be found in Pan-Europe. Long-term seasonal variability of agriculture and forest emissions was taken into account by implementing a new growing season concept. The 2004-2005 averaged annual total biogenic volatile organic compound (BVOC) emissions for the Pan-European domain are estimated to be about 12 Tg with a large contribution from the OVOC class of about 4.5 Tg and from monoterpenes of about 4 Tg. Annual isoprene emissions are found to be about 3.5 Tg, insensitive to the chosen emission algorithm. Emissions of OVOC were found to originate to a large extent from agriculture. Further experiments on crop emissions should be carried out to check the validity of the applied standard emission factors. The new inventory aims at a fully transparent and verifiable aggregation of detailed land use information and at the inclusion of plant-specific emission data. Though plant-specific land use data is available with relatively high accuracy, a lack of experimental biomass densities and emission data on terpenes, sesquiterpenes and oxygenated VOC, in particular for agricultural plants, currently limits the setup of a highly accurate plant-specific emission inventory.

  8. Nuclear medicine annual 1990

    SciTech Connect

    Freeman, L.M. )

    1990-01-01

    Two of the major areas of cutting-edge nuclear medicine research, single-photon emission computed tomography (SPECT) functional brain imaging and monoclonal antibody studies receive attention in this volume. Advances in these areas are critical to the continued growth of our specialty. Fortunately, the current outlook in both areas remains quite optimistic. As has been the policy in the first decade of publication, thorough state-of-the-art reviews on existing procedures are interspersed with chapters dealing with research developments. The editor wishes to express a particular note of appreciation to a very supportive British colleague, Dr. Ignac Fogelman, who is becoming a regular contributor. His exhaustive review of the role of nuclear medicine in the evaluation of osteoporotic patients is packed with extremely useful information that will prove to be fruitful to all readers. The author would like to thank the readers and colleagues who have taken the time to offer useful and constructive comments over the past ten years. The author continue to welcome suggestions that will help to further improve this Annual.

  9. 40 CFR 61.24 - Annual reporting requirements.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 8 2011-07-01 2011-07-01 false Annual reporting requirements. 61.24 Section 61.24 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS National Emission Standards for...

  10. 40 CFR 61.254 - Annual reporting requirements.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 8 2010-07-01 2010-07-01 false Annual reporting requirements. 61.254 Section 61.254 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS National Emission Standards for...

  11. 40 CFR 61.254 - Annual reporting requirements.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 8 2011-07-01 2011-07-01 false Annual reporting requirements. 61.254 Section 61.254 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS National Emission Standards for...

  12. 40 CFR 61.24 - Annual reporting requirements.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 8 2010-07-01 2010-07-01 false Annual reporting requirements. 61.24 Section 61.24 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS National Emission Standards for...

  13. 40 CFR 61.24 - Annual reporting requirements.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 9 2013-07-01 2013-07-01 false Annual reporting requirements. 61.24 Section 61.24 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS National Emission Standards for...

  14. 40 CFR 61.24 - Annual reporting requirements.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 9 2014-07-01 2014-07-01 false Annual reporting requirements. 61.24 Section 61.24 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS National Emission Standards for...

  15. 40 CFR 61.254 - Annual reporting requirements.