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

    PubMed Central

    Bahn, M.; Reichstein, M.; Davidson, E. A.; Grünzweig, 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

  3. 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...

  4. Total OH reactivity emissions from Norway spruce

    NASA Astrophysics Data System (ADS)

    Nölscher, Anke; Bourtsoukidis, Efstratios; Bonn, Boris; Kesselmeier, Jürgen; Lelieveld, Jos; Williams, Jonathan

    2013-04-01

    Forest emissions represent a strong potential sink for the main tropospheric oxidant, the hydroxyl radical (OH). In forested environments, the comparison of the directly determined overall sink of OH radicals, the total OH reactivity, and the individually measured OH sink compounds often exposes a significant gap. This "missing" OH reactivity can be high and influenced by both direct biogenic emissions and secondary photo-oxidation products. To investigate the source of the missing OH sinks in forests, total OH reactivity emission rates were determined for the first time from a Norway spruce (Picea abies) throughout spring, summer and autumn 2011. The total OH reactivity was measured inside a branch enclosure using the Comparative Reactivity Method (CRM) with a Proton Transfer Reaction-Mass Spectrometer (PTR-MS) as the detector. In parallel, separate volatile organic compounds (VOC) emission rates were monitored by a second PTR-MS, including the signal of isoprene, acetaldehyde, total monoterpenes and total sesquiterpenes. The comparison of known and PTR-MS detected OH sink compounds and the directly measured total OH reactivity emitted from Norway spruce revealed unmeasured and possibly unknown primary biogenic emissions. These were found to be highest in late summer during daytime coincident with highest temperatures and ozone levels.

  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. Seasonal and inter-annual variation in ecosystem scale methane emission from a boreal fen

    NASA Astrophysics Data System (ADS)

    Rinne, Janne; Li, Xuefei; Raivonen, Maarit; Peltola, Olli; Sallantaus, Tapani; Haapanala, Sami; Smolander, Sampo; Alekseychik, Pavel; Aurela, Mika; Korrensalo, Aino; Mammarella, Ivan; Tuittila, Eeva-Stiina; Vesala, Timo

    2016-04-01

    Northern wetlands are one of the major sources of atmospheric methane. We have measured ecosystem scale methane emissions from a boreal fen continuously since 2005. The site is an oligotrophic fen in boreal vegetation zone situated in Siikaneva wetland complex in Southern Finland. The mean annual temperature in the area is 3.3°C and total annual precipitation 710 mm. We have conducted the methane emission measurements by the eddy covariance method. Additionally we have measured fluxes of carbon dioxide, water vapor, and sensible heat together with a suite of other environmental parameters. We have analyzed this data alongside with a model run with University of Helsinki methane model. The measured fluxes show generally highest methane emission in late summers coinciding with the highest temperatures in saturated peat zone. During winters the fluxes show small but detectable emission despite the snow and ice cover on the fen. More than 90% of the annual methane emission occurs in snow-free period. The methane emission and peat temperature are connected in exponential manner in seasonal scales, but methane emission does not show the expected behavior with water table. The lack of water table position dependence also contrasts with the spatial variation across microtopography. There is no systematic variation in sub-diurnal time scale. The general seasonal cycle in methane emission is captured well with the methane model. We will show how well the model reproduces the temperature and water table position dependencies observed. The annual methane emission is typically around 10 gC m-2. This is a significant part of the total carbon exchange between the fen and the atmosphere and about twice the estimated carbon loss by leaching from the fen area. The inter-annual variability in the methane emission is modest. The June-September methane emissions from different years, comprising most of the annual emission, correlates positively with peat temperature, but not with

  8. 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.

  9. National annual dioxin emissions estimate for hazardous waste incinerators

    SciTech Connect

    Cudahy, J.J.; Rigo, H.G.

    1997-12-31

    On April 19, 1996, the EPA proposed Maximum Achievable Control [MACT] Standards for Hazardous Waste Combustors. In that preamble, the EPA stated that annual estimated emissions of dioxins from the nation`s hazardous waste incinerators [HWIs] expressed as an equivalent amount of 2,3,7,8 TCDD (international toxic equivalents) are 77 grams. Commentors on EPA dioxin emission estimates from medical waste incinerators and cement kilns found them significantly overestimated. This paper presents an independent dioxin emissions estimate that takes advantage of correcting the errors in EPA`s HWI emissions database, an updated inventory of HWIs in the United States and statistical imputation techniques that maximum the information extractable from the limited dioxin emissions data for HWIs. Actual HWI dioxin emissions are probably between a quarter and half the HWC preamble estimate.

  10. 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.

  11. National annual dioxin emissions estimate for hazardous waste incinerators

    PubMed

    Cudahy; Rigo

    1998-11-01

    Reducing emissions of polychlorinated dibenzo-p-dioxins and dibenzofurans, commonly known as dioxins, is a high priority for environmental regulatory bodies throughout much of the world. In the United States, Section 112 (c)(6) of the Clean Air Act (CAA) requires the Environmental Protection Agency (EPA) to identify and control emissions from sources that are responsible for at least 90% of the overall emissions of seven targeted hazardous air pollutants, including dioxins. On April 19, 1996, the EPA proposed Maximum Achievable Control Technology (MACT) Standards for Hazardous Waste Combustors (HWCs). In that preamble, the EPA estimated annual dioxin emissions from the nation's hazardous waste incinerators (HWIs) to be 79 grams expressed as 2,3,7,8 tetrachloro dibenzo-p-dioxins (TCDD) international toxic equivalents (ITEQs). However, early EPA dioxin emission estimates from medical waste incinerators and cement kilns were significantly overestimated; so, the following independent national dioxin emissions estimate for HWIs was prepared. This estimate corrects the errors in the EPA's HWI emissions database, uses an updated inventory of HWIs in the United States, and applies statistical imputation techniques that take maximum advantage of the limited dioxin emissions data for HWIs.

  12. 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.

  13. 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.

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

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 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, 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...

  16. 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.

  17. 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...

  18. 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...

  19. 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.

  20. 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.

  1. 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

    2016-10-01

    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.

  2. 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...

  3. 40 CFR 97.424 - Compliance with TR NOX Annual emissions limitation.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 22 2012-07-01 2012-07-01 false Compliance with TR NOX Annual... (CONTINUED) AIR PROGRAMS (CONTINUED) FEDERAL NOX BUDGET TRADING PROGRAM AND CAIR NOX AND SO2 TRADING PROGRAMS TR NOX Annual Trading Program § 97.424 Compliance with TR NOX Annual emissions limitation....

  4. 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)

  5. 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.

  6. 40 CFR 57.303 - Total plantwide emission limitation.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... plantwide emission limitation. (a) Calculation of the emission limitation. Each NSO shall contain a... August 7, 1977. This limitation shall be expressed in units of mass per time and shall be calculated as... direct measurements or appropriately documented mass balance calculations. (b) Compliance with...

  7. 40 CFR 57.303 - Total plantwide emission limitation.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... plantwide emission limitation. (a) Calculation of the emission limitation. Each NSO shall contain a... August 7, 1977. This limitation shall be expressed in units of mass per time and shall be calculated as... direct measurements or appropriately documented mass balance calculations. (b) Compliance with...

  8. 40 CFR 57.303 - Total plantwide emission limitation.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... plantwide emission limitation. (a) Calculation of the emission limitation. Each NSO shall contain a... August 7, 1977. This limitation shall be expressed in units of mass per time and shall be calculated as... direct measurements or appropriately documented mass balance calculations. (b) Compliance with...

  9. 29 CFR 779.253 - What is included in computing the total annual inflow volume.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 29 Labor 3 2013-07-01 2013-07-01 false What is included in computing the total annual inflow volume. 779.253 Section 779.253 Labor Regulations Relating to Labor (Continued) WAGE AND HOUR DIVISION... Apply; Enterprise Coverage Interstate Inflow Test Under Prior Act § 779.253 What is included...

  10. 29 CFR 779.253 - What is included in computing the total annual inflow volume.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 29 Labor 3 2014-07-01 2014-07-01 false What is included in computing the total annual inflow volume. 779.253 Section 779.253 Labor Regulations Relating to Labor (Continued) WAGE AND HOUR DIVISION... Apply; Enterprise Coverage Interstate Inflow Test Under Prior Act § 779.253 What is included...

  11. 29 CFR 779.253 - What is included in computing the total annual inflow volume.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 29 Labor 3 2012-07-01 2012-07-01 false What is included in computing the total annual inflow volume. 779.253 Section 779.253 Labor Regulations Relating to Labor (Continued) WAGE AND HOUR DIVISION... Apply; Enterprise Coverage Interstate Inflow Test Under Prior Act § 779.253 What is included...

  12. 40 CFR 57.303 - Total plantwide emission limitation.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... August 7, 1977. This limitation shall be expressed in units of mass per time and shall be calculated as... direct measurements or appropriately documented mass balance calculations. (b) Compliance with the emission limitation. Each NSO shall require the use of specific, enforceable testing methods...

  13. 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

  14. 40 CFR 97.424 - Compliance with TR NOX Annual emissions limitation.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 21 2014-07-01 2014-07-01 false Compliance with TR NOX Annual emissions limitation. 97.424 Section 97.424 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... accounting basis in the following order: (i) Any TR NOX Annual allowances that were allocated to the units...

  15. 40 CFR 97.424 - Compliance with TR NOX Annual emissions limitation.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 22 2013-07-01 2013-07-01 false Compliance with TR NOX Annual emissions limitation. 97.424 Section 97.424 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... accounting basis in the following order: (i) Any TR NOX Annual allowances that were allocated to the units...

  16. 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

  17. 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 PROTECTION TRUTH IN LENDING (REGULATION Z) Pt. 1026, App. K Appendix K to Part 1026—Total Annual Loan...

  18. 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 PROTECTION TRUTH IN LENDING (REGULATION Z) Pt. 1026, App. K Appendix K to Part 1026—Total Annual Loan...

  19. 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 Reverse Mortgage Transactions K Appendix K to Part 226 Banks and Banking FEDERAL RESERVE SYSTEM (CONTINUED..., App. K Appendix K to Part 226—Total Annual Loan Cost Rate Computations for Reverse...

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

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 12 Banks and Banking 3 2013-01-01 2013-01-01 false Total Annual Loan Cost Rate Computations for Reverse Mortgage Transactions K Appendix K to Part 226 Banks and Banking FEDERAL RESERVE SYSTEM (CONTINUED..., App. K Appendix K to Part 226—Total Annual Loan Cost Rate Computations for Reverse...

  1. Total prompt γ-ray emission in fission

    NASA Astrophysics Data System (ADS)

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

    2016-06-01

    The total prompt γ-ray energy distributions for the neutron-induced fission of 235U, 239,241Pu at incident neutron energy of 0.025 eV ‒ 100 keV, and the spontaneous fission of 252Cf were measured using the Detector for Advanced Neutron Capture Experiments (DANCE) array 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. The mean values of the total prompt γ-ray energy, determined from the unfolded distributions, are ~ 20% higher than those derived from measurements using single γ-ray detector for all the fissile nuclei studied. This raises serious concern on the validity of the mean total prompt γ-ray energy obtained from the product of mean values for both prompt γ-ray energy and multiplicity.

  2. 40 CFR 51.321 - Annual source emissions and State action report.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... action report. 51.321 Section 51.321 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS REQUIREMENTS FOR PREPARATION, ADOPTION, AND SUBMITTAL OF IMPLEMENTATION PLANS Reports Source Emissions and State Action Reporting § 51.321 Annual source emissions and State action report....

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

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... factor plan requirements. 63.1431 Section 63.1431 Protection of Environment ENVIRONMENTAL PROTECTION... Polyether Polyols Production § 63.1431 Process vent annual epoxides emission factor plan requirements. (a) Applicability of emission factor plan requirements. An owner or operator electing to comply with an...

  4. Annual variations of odor concentrations and emissions from swine gestation, farrowing, and nursery buildings.

    PubMed

    Guo, Huiqing; Wang, Yuanyuan; Yuan, Yuming

    2011-12-01

    To obtain annual odor emission profiles from intensive swine operations, odor concentrations and emission rates were measured monthly from swine nursery, farrowing, and gestation rooms for a year. Large annual variations in odor concentrations and emissions were found in all the rooms and the impact of the seasonal factor (month) was significant (P < 0.05). Odor concentration was low in summer when ventilation rate was high but high in winter when ventilation rate was low, ranging from 362 (farrowing room in July) to 8934 (nursery room in December) olfactory unit (OU) m(-3). This indicates that the air quality regarding odor was significantly better in summer than that in winter. Odor emission rate did not show obvious seasonal pattern as odor concentration did, ranging from 2 (gestation room in November) to 90 (nursery room in April) OU m(-2) sec(-1); this explains why the odor complaints for swine barns have occurred all year round. The annual geometric mean odor concentration and emission rate of the nursery room was significantly higher than the other rooms (P < 0.05). In order to obtain the representative annual emission rate, measurements have to be taken at least monthly, and then the geometric mean of the monthly values will represent the annual emission rate. Incorporating odor control technologies in the nursery area will be the most efficient in reducing odor emission from the farm considering its emission rate was 2 to 3 times of the other areas. The swine grower-finisher area was the major odor source contributing 53% of odor emission of the farm and should also be targeted for odor control. Relatively positive correlations between odor concentration and both H2S and CO2 concentrations (R(2) = 0.58) means that high level of these two gases might likely indicate high odor concentration in swine barns.

  5. 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

  6. 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

    ... 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 226—Assumed Loan Periods for Computations of Total Annual Loan Cost Rates (a)...

  7. 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

  8. 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.

  9. 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.

  10. 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.

  11. 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.

  12. 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.

  13. 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

  14. 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

  15. Quantification of variability and uncertainty in lawn and garden equipment NOx and total hydrocarbon emission factors.

    PubMed

    Frey, H Christopher; Bammi, Sachin

    2002-04-01

    Variability refers to real differences in emissions among multiple emission sources at any given time or over time for any individual emission source. Variability in emissions can be attributed to variation in fuel or feedstock composition, ambient temperature, design, maintenance, or operation. Uncertainty refers to lack of knowledge regarding the true value of emissions. Sources of uncertainty include small sample sizes, bias or imprecision in measurements, nonrepresentativeness, or lack of data. Quantitative methods for characterizing both variability and uncertainty are demonstrated and applied to case studies of emission factors for lawn and garden (L&G) equipment engines. Variability was quantified using empirical and parametric distributions. Bootstrap simulation was used to characterize confidence intervals for the fitted distributions. The 95% confidence intervals for the mean grams per brake horsepower/hour (g/hp-hr) emission factors for two-stroke engine total hydrocarbon (THC) and NOx emissions were from -30 to +41% and from -45 to +75%, respectively. The confidence intervals for four-stroke engines were from -33 to +46% for THCs and from -27 to +35% for NOx. These quantitative measures of uncertainty convey information regarding the quality of the emission factors and serve as a basis for calculation of uncertainty in emission inventories (EIs).

  16. 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

  17. 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...

  18. 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...

  19. 40 CFR 63.1431 - Process vent annual epoxides emission factor plan requirements.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... group determination procedures in the NESHAP for Group I Polymers and Resins (40 CFR part 63, subpart U..., recovery, or recapture device, along with the expected percent efficiency. (iii) Annual emissions after the... section, kg/yr. R = Expected control efficiency of the combustion, recovery, or recapture device,...

  20. 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... AGENCY Notice of Annual Adjustment of the Cap on Average Total Assets That Defines Community Financial... Agency (FHFA) has adjusted the cap on average total assets that defines a ``Community...

  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... AGENCY Notice of Annual Adjustment of the Cap on Average Total Assets That Defines Community Financial... Agency (FHFA) has adjusted the cap on average total assets that defines a ``Community...

  2. 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.

  3. 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.

  4. 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

  5. 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.

  6. 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

  7. 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.

  8. 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.

  9. The Total Hemispheric Emissivity of Painted Aluminum Honeycomb at Cryogenic Temperatures

    NASA Technical Reports Server (NTRS)

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

    2013-01-01

    NASA uses high-emissivity surfaces on deep-space radiators or 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.

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

    NASA Astrophysics Data System (ADS)

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

    2014-01-01

    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.

  11. 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.

  12. 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...

  13. 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...

  14. 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...

  15. Particle size distribution characteristics of cotton gin 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...

  16. 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...

  17. 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...

  18. 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...

  19. 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...

  20. 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...

  1. 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...

  2. Particle size distribution characteristics of cotton gin unloading 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...

  3. 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...

  4. Particle size distribution characteristics of cotton gin second stage 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...

  5. 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

  6. 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.

  7. 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

    ... FDIC invited public comment on proposed rules in January of 2012.\\9\\ \\9\\ Annual Stress Test, 77 FR 3408 (Jan. 24, 2012) (OCC); Annual Stress Test, 77 FR 3166 (Jan. 17, 2012) (FDIC). The Board is finalizing... the Board as specified in the Capital Assessments and Stress Testing information collection (FR...

  8. 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 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....

  9. 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

    ... Reverse Mortgage Transactions K Appendix K 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. K Appendix K to Part 226—Total Annual Loan Cost Rate Computations for Reverse Mortgage Transactions...

  10. 12 CFR Appendix K to Part 226 - Total Annual Loan Cost Rate Computations for Reverse Mortgage Transactions

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... Reverse Mortgage Transactions K Appendix K 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. K Appendix K to Part 226—Total Annual Loan Cost Rate Computations for Reverse Mortgage Transactions...

  11. 12 CFR Appendix K to Part 226 - Total Annual Loan Cost Rate Computations for Reverse Mortgage Transactions

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... Reverse Mortgage Transactions K Appendix K 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. K Appendix K to Part 226—Total Annual Loan Cost Rate Computations for Reverse Mortgage Transactions...

  12. 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

  13. 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.

  14. [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

  15. Contribution of winter to the annual CH4 emission from a eutrophied boreal lake.

    PubMed

    Huttunen, Jari T; Alm, Jukka; Saarijärvi, Erkki; Lappalainen, K Matti; Silvola, Jouko; Martikainen, Pertti J

    2003-01-01

    The springtime methane (CH4) emission from a small, eutrophied boreal lake was assessed during the winter ice-cover by measurement of gas ebullition and CH4 accumulation in the water column in association with the development of oxygen depletion after ice formation. The winter CH4 production was estimated to result in a loss of 3.6-7.9 g CH4 m(-2) from the lake to the atmosphere during the short period of ice melt. This could account for 22-48% of the annual CH4 emission from the pelagic zone of the lake. The contribution of winter to the annual CH4 release can be similar or even higher in seasonally ice-covered northern aquatic ecosystems than in northern terrestrial wetlands, thus winter must be considered in any studies into the aquatic CH4 emissions. The trophic state and wintertime oxygen conditions, linked to the changes in land-use in the catchments and climate, are important factors controlling the springtime lake CH4 emissions. PMID:12653296

  16. 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.

  17. 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

  18. 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.

  19. 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.

  20. 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

    ... 40 Protection of Environment 22 2012-07-01 2012-07-01 false 4 of Subpart W-Default Total Hydrocarbon Emission Factors for Underground Natural Gas Storage W Table W Protection of Environment... Total Hydrocarbon Emission Factors for Underground Natural Gas Storage Underground natural gas...

  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

    ... 40 Protection of Environment 22 2013-07-01 2013-07-01 false 4 of Subpart W of Part 98-Default Total Hydrocarbon Emission Factors for Underground Natural Gas Storage W Table W Protection of... of Part 98—Default Total Hydrocarbon Emission Factors for Underground Natural Gas Storage...

  2. 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

    ... 40 Protection of Environment 22 2012-07-01 2012-07-01 false 3 of Subpart W-Default Total Hydrocarbon Emission Factors for Onshore Natural Gas Transmission Compression W Table W Protection of...—Default Total Hydrocarbon Emission Factors for Onshore Natural Gas Transmission Compression...

  3. 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... of Part 98—Default Total Hydrocarbon Emission Factors for Onshore Natural Gas Processing...

  4. 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... of Part 98—Default Total Hydrocarbon Emission Factors for Underground Natural Gas Storage...

  5. 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

    ... 40 Protection of Environment 22 2013-07-01 2013-07-01 false 2 of Subpart W of Part 98-Default Total Hydrocarbon Emission Factors for Onshore Natural Gas Processing W Table W Protection of... of Part 98—Default Total Hydrocarbon Emission Factors for Onshore Natural Gas Processing...

  6. 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...-3 of Subpart W of Part 98—Default Total Hydrocarbon Emission Factors for Onshore Natural...

  7. 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

    ... 40 Protection of Environment 22 2012-07-01 2012-07-01 false 2 of Subpart W-Default Total Hydrocarbon Emission Factors for Onshore Natural Gas Processing W Table W Protection of Environment... Total Hydrocarbon Emission Factors for Onshore Natural Gas Processing Onshore natural gas...

  8. 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

    ... 40 Protection of Environment 22 2013-07-01 2013-07-01 false 3 of Subpart W of Part 98-Default Total Hydrocarbon Emission Factors for Onshore Natural Gas Transmission Compression W Table W Protection...-3 of Subpart W of Part 98—Default Total Hydrocarbon Emission Factors for Onshore Natural...

  9. 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.

  10. 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.

  11. 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

  12. 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.

  13. 16 CFR 801.11 - Annual net sales and total assets.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... INTERPRETATIONS UNDER THE HART-SCOTT-RODINO ANTITRUST IMPROVEMENTS ACT OF 1976 COVERAGE RULES § 801.11 Annual net... controls, subsidiaries C1 and C2 which B1 controls, and subsidiary C3 which B2 controls. Suppose that A's... sheet of that person. Example: Suppose “A” sells assets to “B” on January 1. “A's” next...

  14. 16 CFR 801.11 - Annual net sales and total assets.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... INTERPRETATIONS UNDER THE HART-SCOTT-RODINO ANTITRUST IMPROVEMENTS ACT OF 1976 COVERAGE RULES § 801.11 Annual net... controls, subsidiaries C1 and C2 which B1 controls, and subsidiary C3 which B2 controls. Suppose that A's... sheet of that person. Example: Suppose “A” sells assets to “B” on January 1. “A's” next...

  15. Regional metropolitan and nonmetropolitan trends in annual growth rates of total personal income and population: 1959-1987.

    PubMed

    Nissan, E

    1992-01-01

    "The annual growth rates of total personal income and population in regional metropolitan and nonmetropolitan areas [of the United States] are examined for the period 1959-87, partitioned into sub periods. Statistical testing for equality of rates shows no perceptible differences in growth rates between the major categories, metro and nonmetro. Further, this study uses a model similar in scope to shift-share analysis to test for convergence of the growth rates within these categories. It was found that for both regional nonmetro and metro areas, there was a general trend toward convergence with the exception of the 1970s decade. In that decade total population growth rates in the nonmetro areas and total income and total population growth rates in the metro areas showed significant divergences."

  16. Mapping mean total annual precipitation in Belgium, by investigating the scale of topographic control at the regional scale

    NASA Astrophysics Data System (ADS)

    Meersmans, J.; Van Weverberg, K.; De Baets, S.; De Ridder, F.; Palmer, S. J.; van Wesemael, B.; Quine, T. A.

    2016-09-01

    Accurate precipitation maps are essential for ecological, environmental, element cycle and hydrological models that have a spatial output component. It is well known that topography has a major influence on the spatial distribution of precipitation and that increasing topographical complexity is associated with increased spatial heterogeneity in precipitation. This means that when mapping precipitation using classical interpolation techniques (e.g. regression, kriging, spline, inverse distance weighting, etc.), a climate measuring network with higher spatial density is needed in mountainous areas in order to obtain the same level of accuracy as compared to flatter regions. In this study, we present a mean total annual precipitation mapping technique that combines topographical information (i.e. elevation and slope orientation) with average total annual rain gauge data in order to overcome this problem. A unique feature of this paper is the identification of the scale at which topography influences the precipitation pattern as well as the direction of the dominant weather circulation. This method was applied for Belgium and surroundings and shows that the identification of the appropriate scale at which topographical obstacles impact precipitation is crucial in order to obtain reliable mean total annual precipitation maps. The dominant weather circulation is determined at 260°. Hence, this approach allows accurate mapping of mean annual precipitation patterns in regions characterized by rather high topographical complexity using a climate data network with a relatively low density and/or when more advanced precipitation measurement techniques, such as radar, aren't available, for example in the case of historical data.

  17. 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

  18. 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

  19. 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…

  20. 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…

  1. 15 CFR 303.3 - Determination of the total annual duty-exemption.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... (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...

  2. 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...

  3. 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...

  4. 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...

  5. 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...

  6. 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.

  7. Constraints on total fire carbon emissions over maritime southeast Asia in 2015

    NASA Astrophysics Data System (ADS)

    Huijnen, Vincent; Wooster, Martin; Kaiser, Johannes; Gaveau, David; Flemming, Johannes; Parrington, Mark; Inness, Antje; Murdiyarso, Daniel; Main, Bruce; van Weele, Michiel

    2016-04-01

    In September and October 2015 widespread forest and peatland fires burned over large parts of maritime southeast Asia, releasing large amounts of terrestrially-stored carbon into the atmosphere, primarily in the form of CO2, CO and CH4. Although seasonal fires are a frequent occurrence in the human modified landscapes in the south of Kalimantan, the southeastern provinces of Sumatra, and West Papua, the extent of the fires was greatly inflated by an extended period of drought associated with a particularly strong El Niño. In this contribution we provide an estimate of the total carbon released in these fires, making use of satellite observations of the fire's radiative power output as processed with GFAS, applied in the modelling and assimilation framework of the Copernicus Atmosphere Monitoring Service (CAMS: http://atmosphere.copernicus.eu/). The carbon emissions are further constrained with MOPITT atmospheric CO column measurements as well as unique on-site plume measurements on Kalimantan. We estimate the carbon emissions from the 2015 fires to be the largest over the maritime southeast Asian region since those associated with the record breaking El Niño of 1997.

  8. 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…

  9. Estimation of maximum annual ambient concentrations of air toxics resulting from industrial facility emissions

    SciTech Connect

    Rehm, R.M. ); Vandenberg, J.J.; Trutna, M.A.; Painter, D.F. )

    1988-01-01

    A screening tool is also needed by S/L agencies and EPA to evaluate initially the large amounts of data now being submitted by industry pursuant to Title III of the Superfund Amendments and Reauthorization Act (SARA) of 1986. Here, while thousands of sources are required to file data submissions on their releases to the environment of over 300 chemicals and classes of compounds, the information on releases to the atmosphere will only include plant-wide, annual stack and fugitive emissions. The result will be a challenge for governmental officials to identify and prioritize source problems in order to effectively respond to inquiries from concerned citizens. Certainly, the screening tool needed for HRPS identification could also be put to constructive use in determining which SARA sources should be analyzed in more detail. This paper summarizes the authors' progress to date in developing this tool.

  10. 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.

  11. The East Siberian Arctic Shelf: monitoring is necessary to assess actual scale of annual methane emissions from seabed deposits. (Invited)

    NASA Astrophysics Data System (ADS)

    Shakhova, N. E.

    2010-12-01

    of strong methane pulses occur, this component is not included in the total flux estimate, which thus is conservative, as the spatial and temporal pattern of such non-gradual “catastrophic event” ebullition is uncertain. Additional components to be incorporated into developed model of annual emissions are following: 1) releases associated with storm events; 2) seasonal releases associated with deep fall convection and ice-break period; 3) winter emissions through flaw polynyas and leads in winter; 4) abrupt releases triggered by seismic and tectonical events, sediments settlement and adjustment associated with permafrost and hydrate destabilization, permafrost breaks, geological power of highly pressured gas fronts. Recent data give evidence that incorporation of only one component (non-gradual releases from hot spot areas) could alter reported numbers many folds. This underscores importance of establishing monitoring net over the ESAS.

  12. 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.

  13. 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.

  14. 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

  15. An interior-point method for total variation regularized positron emission tomography image reconstruction

    NASA Astrophysics Data System (ADS)

    Bai, Bing

    2012-03-01

    There has been a lot of work on total variation (TV) regularized tomographic image reconstruction recently. Many of them use gradient-based optimization algorithms with a differentiable approximation of the TV functional. In this paper we apply TV regularization in Positron Emission Tomography (PET) image reconstruction. We reconstruct the PET image in a Bayesian framework, using Poisson noise model and TV prior functional. The original optimization problem is transformed to an equivalent problem with inequality constraints by adding auxiliary variables. Then we use an interior point method with logarithmic barrier functions to solve the constrained optimization problem. In this method, a series of points approaching the solution from inside the feasible region are found by solving a sequence of subproblems characterized by an increasing positive parameter. We use preconditioned conjugate gradient (PCG) algorithm to solve the subproblems directly. The nonnegativity constraint is enforced by bend line search. The exact expression of the TV functional is used in our calculations. Simulation results show that the algorithm converges fast and the convergence is insensitive to the values of the regularization and reconstruction parameters.

  16. 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.

  17. 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.

  18. 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

  19. 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

  20. Role of the biomass burning emission on the total peroxy nitrates measured during the BORTAS campaign

    NASA Astrophysics Data System (ADS)

    Aruffo, Eleonora; Biancofiore, Fabio; Di Carlo, Piero; Busilacchio, Marcella; Verdecchia, Marco; Tomassetti, Barbara; Dari Salisburgo, Cesare; Giammaria, Franco; Bauguitte, Stephane; Lee, James; Moller, Sarah; Hopkins, James; Punjabi, Shalini; Andrews, Stephen; Lewis, Alistair C.; Palmer, Paul P.; Hyer, Edward; Breton, Michael L.; Percival, Carl

    2016-04-01

    During the BORTAS (BOReal forest fires on Tropospheric oxidants over the Atlantic using Aircraft and Satellites) campaign, carried out in the Eastern Canada during the summer 2011, the total peroxy nitrates (∑PNs) concentrations have been measured using the TD-LIF (Thermal Dissociation - Laser Induced Fluorescence) instrument (Di Carlo et al., 2013) developed at the University of L'Aquila (Italy). In our analysis, we observed a strong correlation between the CO, a well-known BB tracer, and the ∑PNs suggesting the possibility to use also the ∑PNs as BB tracer for the identification of a BB plume. Moreover, Alvarado et al. (2010) demonstrated that, in the first few hours after the emissions by fires, the 40% of the NOx emitted is converted into PAN, confirming that the ∑PNs are strongly produced by BB. We used different methods for the identification of a BB plume using the ∑PNs as a tracer. Moreover, we will show the comparison between our results and the results obtained using other methods available in literature. We will illustrate in detail two case studies in which the ∑PNs and the hydrogen cyanide (HCN) measurements help for a more specific identification of a BB plume. Our results have been confirmed using an artificial neural network model (Biancofiore et al., 2015). References Alvarado, M. J., Logan, J. A., Mao, J., Apel E, Riemer, D., Blake, D., Cohen, R. C., Min, K.-E., Perring, A. E., Browne, E.C., Wooldridge, P. J., Diskin, G. S., Sachse, G.W., Fuelberg, H., Sessions, W. R., Harrigan, D. L., Huey, G., Liao, J., Case-Hanks, A., Jimenez, J. L., Cubison, M. J., Vay, S. A., Weinheimer, A. J., Knapp, D. J., Montzka, D. D., Flocke, F. M., Pollack, I. B., Wennberg, P. O., Kurten, A., Crounse, J., St. Clair, J. M., Wisthaler, A., Mikoviny, T., Yantosca, R. M., Carouge, C. C., and Le Sager, P.: Nitrogen oxides and PAN in plumes from boreal fires during ARCTAS-B and their impact on ozone: an integrated analysis of aircraft and satellite observations

  1. 40 CFR Appendix A to Part 72 - Methodology for Annualization of Emissions Limits

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... expressed in pounds of SO2 per million British Thermal Unit of heat input (lb/mmBtu) and expressed on an... Periods and Annualization Factors Definition Annualization factor Scrubbed Unscrubbed Unit Unit...

  2. 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...

  3. 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...

  4. Mote 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. 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.

  6. 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...

  7. Particle size distribution characteristics of cotton gin first 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...

  8. Particle size distribution characteristics of cotton gin second 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...

  9. 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

  10. 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

  11. 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

  12. 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

  13. The role of midlatitude mixing barriers in creating the annual variation of total ozone in high northern latitudes

    NASA Astrophysics Data System (ADS)

    Gille, John; Karol, Svetlana; Kinnison, Douglas; Lamarque, Jean-Francois; Yudin, Valery

    2014-08-01

    Data from the HIgh Resolution Dynamics Limb Sounder (HIRDLS), the Microwave Limb Sounder (MLS), and the Whole Atmosphere Community Climate Model (WACCM) are used to investigate the annual variation of total column ozone in high northern latitudes. Downward transport of ozone-rich air by the residual mean circulation during autumn and winter bends ozone isopleths down and increases the high-latitude ozone amounts, leading to an ozone maximum at the end of the winter. During the summer months eddy mixing acts to restore pre-fall distributions of ozone. In this study the large-scale mixing in the lower stratosphere is analyzed using Nakamura's (1996) equivalent length formulation with observed and simulated ozone. The analysis of ozone mixing is performed in the tracer equivalent latitude-potential temperature coordinate system. Steep latitudinal gradients of ozone isopleths below about 500 K occur during the winter, where there are minima in the equivalent length, indicating barriers to mixing at 30°N-40°N. This transport barrier allows large ozone maxima to develop poleward of it. The barrier disappears over the summer, permitting latitudinal mixing of the high ozone air. Above 500 K mixing is more effective during the winter, so a large winter maximum does not occur. In both midlatitude and high latitude the lower stratospheric layer from 330 to 500 K doubles its ozone content from autumn to spring, compared with much smaller changes in the layer from 500 to 650 K. Our results confirm that the presence of the winter transport barrier in the lower stratosphere controls the seasonal variation of total ozone.

  14. Electrochemical monitoring of the fluorescence emission of tetrazine and bodipy dyes using total internal reflection fluorescence microscopy coupled to electrochemistry.

    PubMed

    Miomandre, F; Lépicier, E; Munteanu, S; Galangau, O; Audibert, J F; Méallet-Renault, R; Audebert, P; Pansu, R B

    2011-03-01

    A very sensitive technique where an electrochemical cell is coupled to a total internal reflection fluorescence microscopy setup is described and applied for the first time to the electrochemical monitoring of the fluorescence of organic dyes in solution. It is shown that this setup basically allows both spatial and time resolution for the recorded fluorescence signal as a function of the electrode potential: indeed the variations of the emission intensity are recorded within the diffusion layer for a classical cyclic voltammetry or chronoamperometry experiment inducing the redox conversion of an emissive form into a non emissive one (and conversely). Simultaneously, the variations of the emissive state lifetime are measured to discriminate between a mechanism involving only the conversion into a non emissive form from one involving a quenching between the emitter and the electrogenerated species. The results concerning the investigation of the electrochemical monitoring of the fluorescence properties for two types of original dyes are presented, demonstrating the possibility to switch on and off the emission in a fully reversible way and to investigate in depth the mechanisms associated to this switch.

  15. Estimating total aqueous and airborne chemical emissions from ozonated and chemically treated cooling towers

    SciTech Connect

    Pryor, A.

    1996-10-01

    Cooling tower operations result in aqueous and airborne emissions into the environment in the form of blowdown and drift, respectively. Increased regulatory and licensing requirements often obligate end users to quantify the nature and amount of any added chemicals in such emissions. This paper presents a methodology whereby cooling tower operators can perform such calculations for conventionally chemically treated cooling towers as well as ozonated cooling towers. Emissions from cooling towers depend on the operating characteristics of the tower (recirculation rate, drift rate), makeup and cooling water quality (makeup water mineral concentration, cooling water cycles of concentration), the amount of chemicals added to the cooling water, and/or the amount of ozone injected into the cooling water and the mass transfer efficiency of the ozone injection process.

  16. 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.

  17. 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

  18. 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

  19. 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

  20. 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

  1. 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.

  2. 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...

  3. 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.

  4. Plant-specific correlations to predict the total VOC emissions from wastewater treatment plants

    NASA Astrophysics Data System (ADS)

    Oskouie, Ali K.; Lordi, David T.; Granato, Thomas C.; Kollias, Louis

    Simple linear correlations between the lumped parameter of raw wastewater flow rate, mixed liquor suspended solids (MLSS), and concentration of three volatile organic compounds (VOCs), chloroform, dichloromethane and toluene in the liquid and gas phases, Q×MLSS(C/ER), and T, wastewater temperature, were found for three large wastewater treatment plants operated by the Metropolitan Water Reclamation District of Greater Chicago (MWRDGC) using their monthly data for year 2000. These linear relationships were verified for these three dominant VOCs using the data from years 1987 to 1992, 1998, and 1999 for the three MWRDGC plants. The results of this theoretical study showed that linear functions could reasonably fit to the actual data, and the specific VOC compounds' emission rate could be predicted upon having information on ambient temperature, MLSS, and VOC concentration in the liquid phase at the influent to the specific plant without having to use the Bay Area Sewage Toxics Emission (BASTE) fate model as a future emission estimator once the baseline correlation was determined.

  5. Quantifying missing annual emission sources of heavy metals in the United Kingdom with an atmospheric transport model.

    PubMed

    Dore, Anthony J; Hallsworth, Stephen; McDonald, Alan G; Werner, Małgorzata; Kryza, Maciej; Abbot, John; Nemitz, Eiko; Dore, Christopher J; Malcolm, Heath; Vieno, Massimo; Reis, Stefan; Fowler, David

    2014-05-01

    An atmospheric chemical transport model was adapted to simulate the concentration and deposition of heavy metals (arsenic, cadmium, chromium, copper, lead, nickel, selenium, vanadium, and zinc) in the United Kingdom. The model showed that wet deposition was the most important process for the transfer of metals from the atmosphere to the land surface. The model achieved a good correlation with annually averaged measurements of metal concentrations in air. The correlation with measurements of wet deposition was less strong due to the complexity of the atmospheric processes involved in the washout of particulate matter which were not fully captured by the model. The measured wet deposition and air concentration of heavy metals were significantly underestimated by the model for all metals (except vanadium) by factors between 2 and 10. These results suggest major missing sources of annual heavy metal emissions which are currently not included in the official inventory. Primary emissions were able to account for only 9%, 21%, 29%, 21%, 36%, 7% and 23% of the measured concentrations for As, Cd, Cr, Cu, Ni, Pb and Zn. A likely additional contribution to atmospheric heavy metal concentrations is the wind driven re-suspension of surface dust still present in the environment from the legacy of much higher historic emissions. Inclusion of two independent estimates of emissions from re-suspension in the model was found to give an improved agreement with measurements. However, an accurate estimate of the magnitude of re-suspended emissions is restricted by the lack of measurements of metal concentrations in the re-suspended surface dust layer.

  6. Inter-Annual Variability of Area-Scaled Gaseous Carbon Emissions from Wetland Soils in the Liaohe Delta, China.

    PubMed

    Ye, Siyuan; Krauss, Ken W; Brix, Hans; Wei, Mengjie; Olsson, Linda; Yu, Xueyang; Ma, Xueying; Wang, Jin; Yuan, Hongming; Zhao, Guangming; Ding, Xigui; Moss, Rebecca F

    2016-01-01

    Global management of wetlands to suppress greenhouse gas (GHG) emissions, facilitate carbon (C) sequestration, and reduce atmospheric CO2 concentrations while simultaneously promoting agricultural gains is paramount. However, studies that relate variability in CO2 and CH4 emissions at large spatial scales are limited. We investigated three-year emissions of soil CO2 and CH4 from the primary wetland types of the Liaohe Delta, China, by focusing on a total wetland area of 3287 km2. One percent is Suaeda salsa, 24% is Phragmites australis, and 75% is rice. While S. salsa wetlands are under somewhat natural tidal influence, P. australis and rice are managed hydrologically for paper and food, respectively. Total C emissions from CO2 and CH4 from these wetland soils were 2.9 Tg C/year, ranging from 2.5 to 3.3 Tg C/year depending on the year assessed. Primary emissions were from CO2 (~98%). Photosynthetic uptake of CO2 would mitigate most of the soil CO2 emissions, but CH4 emissions would persist. Overall, CH4 fluxes were high when soil temperatures were >18°C and pore water salinity <18 PSU. CH4 emissions from rice habitat alone in the Liaohe Delta represent 0.2% of CH4 carbon emissions globally from rice. With such a large area and interannual sensitivity in soil GHG fluxes, management practices in the Delta and similar wetlands around the world have the potential not only to influence local C budgeting, but also to influence global biogeochemical cycling.

  7. Inter-Annual Variability of Area-Scaled Gaseous Carbon Emissions from Wetland Soils in the Liaohe Delta, China.

    PubMed

    Ye, Siyuan; Krauss, Ken W; Brix, Hans; Wei, Mengjie; Olsson, Linda; Yu, Xueyang; Ma, Xueying; Wang, Jin; Yuan, Hongming; Zhao, Guangming; Ding, Xigui; Moss, Rebecca F

    2016-01-01

    Global management of wetlands to suppress greenhouse gas (GHG) emissions, facilitate carbon (C) sequestration, and reduce atmospheric CO2 concentrations while simultaneously promoting agricultural gains is paramount. However, studies that relate variability in CO2 and CH4 emissions at large spatial scales are limited. We investigated three-year emissions of soil CO2 and CH4 from the primary wetland types of the Liaohe Delta, China, by focusing on a total wetland area of 3287 km2. One percent is Suaeda salsa, 24% is Phragmites australis, and 75% is rice. While S. salsa wetlands are under somewhat natural tidal influence, P. australis and rice are managed hydrologically for paper and food, respectively. Total C emissions from CO2 and CH4 from these wetland soils were 2.9 Tg C/year, ranging from 2.5 to 3.3 Tg C/year depending on the year assessed. Primary emissions were from CO2 (~98%). Photosynthetic uptake of CO2 would mitigate most of the soil CO2 emissions, but CH4 emissions would persist. Overall, CH4 fluxes were high when soil temperatures were >18°C and pore water salinity <18 PSU. CH4 emissions from rice habitat alone in the Liaohe Delta represent 0.2% of CH4 carbon emissions globally from rice. With such a large area and interannual sensitivity in soil GHG fluxes, management practices in the Delta and similar wetlands around the world have the potential not only to influence local C budgeting, but also to influence global biogeochemical cycling. PMID:27501148

  8. Inter-Annual Variability of Area-Scaled Gaseous Carbon Emissions from Wetland Soils in the Liaohe Delta, China

    PubMed Central

    Ye, Siyuan; Krauss, Ken W.; Brix, Hans; Wei, Mengjie; Olsson, Linda; Yu, Xueyang; Ma, Xueying; Wang, Jin; Yuan, Hongming; Zhao, Guangming; Ding, Xigui; Moss, Rebecca F.

    2016-01-01

    Global management of wetlands to suppress greenhouse gas (GHG) emissions, facilitate carbon (C) sequestration, and reduce atmospheric CO2 concentrations while simultaneously promoting agricultural gains is paramount. However, studies that relate variability in CO2 and CH4 emissions at large spatial scales are limited. We investigated three-year emissions of soil CO2 and CH4 from the primary wetland types of the Liaohe Delta, China, by focusing on a total wetland area of 3287 km2. One percent is Suaeda salsa, 24% is Phragmites australis, and 75% is rice. While S. salsa wetlands are under somewhat natural tidal influence, P. australis and rice are managed hydrologically for paper and food, respectively. Total C emissions from CO2 and CH4 from these wetland soils were 2.9 Tg C/year, ranging from 2.5 to 3.3 Tg C/year depending on the year assessed. Primary emissions were from CO2 (~98%). Photosynthetic uptake of CO2 would mitigate most of the soil CO2 emissions, but CH4 emissions would persist. Overall, CH4 fluxes were high when soil temperatures were >18°C and pore water salinity <18 PSU. CH4 emissions from rice habitat alone in the Liaohe Delta represent 0.2% of CH4 carbon emissions globally from rice. With such a large area and interannual sensitivity in soil GHG fluxes, management practices in the Delta and similar wetlands around the world have the potential not only to influence local C budgeting, but also to influence global biogeochemical cycling. PMID:27501148

  9. 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

  10. 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

  11. 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).

  12. Readily implementable techniques can cut annual CO2 emissions from the production of concrete by over 20%

    NASA Astrophysics Data System (ADS)

    Miller, Sabbie A.; Horvath, Arpad; Monteiro, Paulo J. M.

    2016-07-01

    Due to its prevalence in modern infrastructure, concrete is experiencing the most rapid increase in consumption among globally common structural materials; however, the production of concrete results in approximately 8.6% of all anthropogenic CO2 emissions. Many methods have been developed to reduce the greenhouse gas emissions associated with the production of concrete. These methods range from the replacement of inefficient manufacturing equipment to alternative binders and the use of breakthrough technologies; nevertheless, many of these methods have barriers to implementation. In this research, we examine the extent to which the increased use of several currently implemented methods can reduce the greenhouse gas emissions in concrete material production without requiring new technologies, changes in production, or novel material use. This research shows that, through increased use of common supplementary cementitious materials, appropriate selection of proportions for cement replacement, and increased concrete design age, 24% of greenhouse gas emissions from global concrete production or 650 million tonnes (Mt) CO2-eq can be eliminated annually.

  13. Operating costs for reducing total emission loads of key pollutants in municipal wastewater treatment plants in China.

    PubMed

    Wang, J W; Zhang, T Z; Chen, J N

    2010-01-01

    Total emission load reduction of COD, NH(4)-N, TN, and TP is the key measure in controlling water pollution and eutrophication. Municipal wastewater treatment plants (MWWTPs) are major contributors in lowering energy consumption and reducing pollutant discharge. The flow-based operating costs have not been directly established to relate to costs of pollutant reduction based on an investigation of 11 MWWTPs in China. However, energy consumption to eliminate one kilogram of COD or NH(4)-N was observed to decrease when the total reduced pollutants is increased. Additional energy consumption required to remove nitrogen and phosphorus is allotted for mixers and internal return pumps. Major factors for operating costs include influent and effluent concentration, design capacity, and flow loading rate. Therefore, an operating cost model for the total emission load reduction of COD, NH(4)-N, TN, and TP was developed based on energy consumption and the above mentioned major factors. Using this model to calculate the operating costs for MWWTPs would facilitate more reduction of key pollutants than the flow-based method.

  14. 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.

  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. 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.

  17. Hydropower’s Contribution to Carbon Dioxide Emission Reduction

    SciTech Connect

    Francfort, James E.

    1997-11-01

    The annual carbon dioxide emissions currently (1997 figures) avoided by the use of hydropower in electricity generation is 142 million metric tons, and it has a carbon tax value of $7.1 billion. Developing the identified additional hydropower capacity can yield an additional 34 million tons annually of avoided carbon dioxide emissions, with a value of $1.7 billion in carbon taxes. The total annual avoided emissions can exceed 176 million metric tons, with a value of $8.8 billion.

  18. 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.

  19. Avoiding total reduced sulfur (TRS) emissions from sodium sulfite pulping recovery processes

    SciTech Connect

    Norman, J.C.; Sell, N.J. ); Ciriacks, J.C. )

    1990-06-01

    This paper reports that one of the current trends in paper-making with cellulose pulping is the use of high-yield processes. With yields greater than 65%, these processes include mechanical pulps (groundwood and thermomechanical pulps or TMP), and semichemical types (chemi-TMP or CTMP). Groundwood and TMP make up about 10% of North American pulp production. Semichemical pulp makes up about 7% and is mostly used for corrugating medium. High-yield pulping for linerboard, particularly using the alkaline sulfite process, is also likely to be used in the future. High-yield pulping is based primarily on the sulfite process using mostly sodium-based chemicals. A disadvantage of this process is the unavailability of a recovery system for the inorganic pulping chemicals. Generally, mills have not accepted any particular recovery system for this process. For this and other reasons, sulfite processes constitute only 3-4% of the total North American pulp production. If high-yield processes continue to increase in popularity, a sodium sulfite chemical recovery system will be needed. A number of chemical recovery systems have been developed in the past 30 years for sodium-based sulfite pulping processes, with most of the mills successfully using this process located in Scandinavia.

  20. 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.

  1. 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

  2. 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.

  3. 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

  4. 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...

  5. 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.

  6. 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.

  7. Non-native plant litter enhances soil carbon dioxide emissions in an invaded annual grassland.

    PubMed

    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

  8. 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.

  9. Simple approximation of total emissivity of CO2-H2O mixture used in the zonal method of calculation of heat transfer by radiation

    NASA Astrophysics Data System (ADS)

    Lisienko, V. G.; Malikov, G. K.; Titaev, A. A.

    2014-12-01

    The paper presents a new simple-to-use expression to calculate the total emissivity of a mixture of gases CO2 and H2O used for modeling heat transfer by radiation in industrial furnaces. The accuracy of this expression is evaluated using the exponential wide band model. It is found that the time taken to calculate the total emissivity in this expression is 1.5 times less than in other approximation methods.

  10. 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

  11. 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

  12. 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.

  13. 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.

  14. 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.

  15. 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…

  16. 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.

  17. Examination of rotational fixation of the femoral component in total hip arthroplasty. A mechanical study of micromovement and acoustic emission.

    PubMed

    Sugiyama, H; Whiteside, L A; Kaiser, A D

    1989-12-01

    Rotational loosening has recently emerged as an important cause of failure of the femoral component of total hip arthroplasties. This study was designed to investigate the role played by torsional loads in loosening of cementless femoral components and to evaluate three cementing techniques involving a combination of canal irrigation, manual insertion, and vacuum mixing combined with pressure injection of the cement for their ability to improve rotational fixation. Rotational micromotion and subsidence were measured in 24 preserved human anatomic specimen femora. Acoustic emission (AE) technique was applied as a non-destructive method for evaluating material failure during loading. From the micromovement data, torque to 50 mu subsidence and torque to failure were surprisingly low with cementless fixation and with poor cement technique but were markedly improved with pulsed irrigation. Further improvement was achieved by pressure injection and vacuum mixing of the cement. However, AE was detected even in the most carefully performed cement specimens under torsional-loading conditions commonly occurring in daily activities. These signs of microfailure of the cement mantle at relatively low torsional loads suggest that the mode of failure of deeply penetrated cement is by microfracture of the cement mantle. The poor performance suggests that cementless fixation of intramedullary stems provides unsatisfactory fixation against torsional loading. There is need for major improvements in fixation mechanisms and techniques. The signs of failure of the cement mantle at normally occurring torsional loads suggest that even the best cement technique is prone to failure in torsion when exposed to normal daily use. PMID:2582663

  18. Development of a tunable diode laser absorption sensor for online monitoring of industrial gas total emissions based on optical scintillation cross-correlation technique.

    PubMed

    Zhang, Zhirong; Pang, Tao; Yang, Yang; Xia, Hua; Cui, Xiaojuan; Sun, Pengshuai; Wu, Bian; Wang, Yu; Sigrist, Markus W; Dong, Fengzhong

    2016-05-16

    We report the first application of gas total emission using a DFB diode laser for gas concentration measurements combined with two LEDs for gas velocity measurements. In situ gas total emissions and particle density measurements in an industrial pipeline using simultaneous tunable diode laser absorption spectroscopy (TDLAS) and optical scintillation cross-correlation technique (OSCC) are presented. Velocity mean values obtained are 7.59 m/s (OSCC, standard deviation is 1.37 m/s) and 8.20 m/s (Pitot tube, standard deviation is 1.47 m/s) in a steel plant pipeline for comparison. Our experiments demonstrate that the combined system of TDLAS and OSCC provides a new versatile tool for accurate measurements of total gas emissions. PMID:27409967

  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. 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.

  1. Fe II EMISSION IN ACTIVE GALACTIC NUCLEI: THE ROLE OF TOTAL AND GAS-PHASE IRON ABUNDANCE

    SciTech Connect

    Shields, Gregory A.; Ludwig, Randi R.; Salviander, Sarah E-mail: randi@astro.as.utexas.ed

    2010-10-01

    Active galactic nuclei (AGNs) have Fe II emission from the broad-line region (BLR) that differs greatly in strength from object to object. We examine the role of the total and gas-phase iron abundance in determining Fe II strength. Using AGN spectra from the Sloan Digital Sky Survey (SDSS) in the redshift range of 0.2 < z < 0.35, we measure the Fe/Ne abundance of the narrow-line region (NLR) using the [Fe VII]/[Ne V] line intensity ratio. We find no significant difference in the abundance of Fe relative to Ne in the NLR as a function of Fe II/H{beta}. However, the [N II]/[S II] ratio increases by a factor of 2 with increasing Fe II strength. This indicates a trend in N/S abundance ratio, and by implication in the overall metallicity of the NLR gas, with increasing Fe II strength. We propose that the wide range of Fe II strength in AGN largely results from the selective depletion of Fe into grains in the low ionization portion of the BLR. Photoionization models show that the strength of the optical Fe II lines varies almost linearly with gas-phase Fe abundance, while the ultraviolet Fe II strength varies more weakly. Interstellar depletions of Fe can be as large as 2 orders of magnitude, sufficient to explain the wide range of optical Fe II strength in AGNs. This picture is consistent with the similarity of the BLR radius to the dust sublimation radius and with indications of Fe II emitting gas flowing inward from the dusty torus.

  2. 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

  3. Speciation of Total Organic Gas and Particulate Matter Emissions from Onroad Vehicles in the Next Version of MOVES

    EPA Science Inventory

    Calculation of organic gas measures used in MOVES (total hydrocarbons, methane, non-methane hydrocarbons, volatile organic compounds, non-methane organic gases, and total organic gases). Incorporation of speciation within MOVES to produce total organic gas and particulate matte...

  4. 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.

  5. 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...

  6. 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.

  7. 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

  8. 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

  9. 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...

  10. Two periods of total testicular regression are peculiar events of the annual reproductive cycle of the black Myotis bat, Myotis nigricans (Chiroptera: Vespertilionidae).

    PubMed

    Beguelini, Mateus R; Góes, Rejane M; Taboga, Sebastião R; Morielle-Versute, Eliana

    2014-01-01

    Myotis nigricans presents few and controversial reproductive data, which indicate geographical variation in reproduction. Thus, this study aimed to evaluate the seasonal modifications in testicular and epididymal morphologies in a tropical environment, submitting these organs to morphometric and immunohistochemical analysis. The observations revealed that this species presents two peaks of spermatogenic activity followed by two periods of total testicular regression (a quiescent pre-pubertal-like morphology, where only Sertoli cells and spermatogonia could be observed), in the same annual reproductive cycle, which seem to be only indirectly influenced by abiotic factors. This testicular behaviour seems to be synchronised with the caput and corpus epididymidis, but not with the cauda epididymidis, which presents aspects of sperm storage in May-June. The control of this variation seems to be directly linked to the expression of the androgen receptor, since, throughout the year, it is high in periods of testicular recrudescence and low in periods of deactivation. It is not thought to be directly linked to apoptosis, which is more pronounced in periods of recrudescence than in periods of regression. PMID:23830483

  11. Response of total belowground carbon flux and soil organic carbon storage to increasing mean annual temperature in Hawaiian tropical montane wet forest.

    NASA Astrophysics Data System (ADS)

    Giardina, C. P.; Litton, C. M.; Crow, S. E.

    2011-12-01

    Controls on the allocation of carbon belowground by plants and the retention of this carbon as new soil organic carbon are poorly quantified, yet exert a large influence on the carbon balance of the terrestrial biosphere. While many studies have now quantified total belowground carbon flux (TBCF), and general global patterns have been identified, rigorous field tests of the effects of climate variables on TBCF do not yet exist, and the conversion of TBCF into soil organic carbon - particularly long-lived soil organic carbon - has received little attention. These represent critical gaps in our understanding of terrestrial carbon cycling, and currently severely constrain efforts to model climate change impacts on belowground carbon processes and storage. We have established a model mean annual temperature gradient spanning 5.2°C in Hawaiian tropical montane wet forests where soil type and age, soil moisture balance, vegetation composition, and disturbance history do not co-vary with temperature. We found that TBCF increases by a factor of two over the 5.2°C MAT gradient in response to increasing ecosystem productivity, while total soil carbon storage is constant. These findings suggest that as temperatures warm, there will be a significant increase in TBCF and belowground carbon process leading to increased flux of CO2 from soils as soil respiration, but that soil organic carbon storage will be relatively insensitive to warming - at least where moisture availability is not affected by rising temperatures. While short-term responses to warming may differ, this study represents long-term insight into the impacts of rising temperatures on belowground carbon cycling and assumes that ecosystem characteristics will change with warming as quantified across this MAT gradient.

  12. 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.

  13. 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).

  14. US Department of Energy radionuclide air emissions annual report (under Subpart H of 40 CFR Part 61) calendar year 1993

    SciTech Connect

    Not Available

    1993-12-31

    This report contains information collected by the Rocky Flats Plant concerning the emission of radionuclides into the air. Topics discussed include: Facility information, source description, air emissions data, dose assessments, point and non-point sources, and supplemental information on decontamination of concrete docks.

  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

  17. Multiple pulse-heating experiments with different current to determine total emissivity, heat capacity, and electrical resistivity of electrically conductive materials at high temperatures.

    PubMed

    Watanabe, Hiromichi; Yamashita, Yuichiro

    2012-01-01

    A modified pulse-heating method is proposed to improve the accuracy of measurement of the hemispherical total emissivity, specific heat capacity, and electrical resistivity of electrically conductive materials at high temperatures. The proposed method is based on the analysis of a series of rapid resistive self-heating experiments on a sample heated at different temperature rates. The method is used to measure the three properties of the IG-110 grade of isotropic graphite at temperatures from 850 to 1800 K. The problem of the extrinsic heating-rate effect, which reduces the accuracy of the measurements, is successfully mitigated by compensating for the generally neglected experimental error associated with the electrical measurands (current and voltage). The results obtained by the proposed method can be validated by the linearity of measured quantities used in the property determinations. The results are in reasonably good agreement with previously published data, which demonstrate the suitability of the proposed method, in particular, to the resistivity and total emissivity measurements. An interesting result is the existence of a minimum in the emissivity of the isotropic graphite at around 1120 K, consistent with the electrical resistivity results.

  18. Evaluation of AERMOD and CALPUFF for predicting ambient concentrations of total suspended particulate matter (TSP) emissions from a quarry in complex terrain.

    PubMed

    Tartakovsky, Dmitry; Broday, David M; Stern, Eli

    2013-08-01

    Concentrations of particulate emissions from a quarry located in hilly terrain were calculated by two common atmospheric dispersion models, AERMOD and CALPUFF. Evaluation of these models for emissions from quarries/open pit mines that are located in complex topography is missing from the literature. Due to severe uncertainties in the input parameters, numerous scenarios were simulated and model sensitivity was studied. Model results were compared among themselves, and to measured total suspended particulate (TSP). For a wide range of meteorological and topographical conditions studied, AERMOD predictions were in a better agreement with the measurements than those obtained by CALPUFF. The use of AERMOD's "Open pit" tool seems unnecessary when accurate digital topographic data are available. Onsite meteorological data are shown to be crucial for reliable dispersion calculations in complex terrain.

  19. The experimental determination of the temperature dependence of the total emissivity of GaAs using a new temperature measurement technique

    NASA Astrophysics Data System (ADS)

    Timans, P. J.

    1992-07-01

    Temperature measurement and control are key issues in many technologically important areas of semiconductor processing, including rapid thermal annealing, molecular-beam epitaxy, and plasma processing. As a result, the development of accurate techniques for the characterization of thermal cycles is a problem of great practical interest. In this study, the total emissivity of specimens of GaAs was determined using a technique which combines isothermal electron-beam heating with a temperature measurement method which exploits the temperature dependence of the band gap of GaAs. Emission spectra from the GaAs specimens were recorded for a range of heating power densities. These spectra display a maximum near the semiconductor absorption edge, because the blackbody radiation rises with increasing wavelength but the spectral emissivity decreases rapidly once the photon energy falls below the band gap. The temperature was determined by fitting the Planck radiation function to the high-energy side of the maximum. This allowed a self-consistent determination of the temperature dependence of the position of the absorption edge. The results were used to calibrate a second set of experiments in which a corresponding set of reflection spectra were recorded. The reflection spectra exhibit a large change in reflectivity at the absorption edge, because light starts being reflected from the back surface of the wafer as well as from the front when it becomes transparent. The reflection spectra provide a convenient method of temperature measurement because the intensity of the reflected light can be much larger than that of the emitted light. The large signal levels should permit temperature measurements to be made with good spatial and temporal resolution, even for samples at low temperatures. The temperature measurements can be performed with a precision of about 2 °C, and in this study the accuracy was ±5 °C. As a result of these measurements the total hemispherical emissivity

  20. 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

  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

    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.

  3. Volcanic Eruption Detection by the Total Ozone Mapping Spectrometer (TOMS) Instruments: a 22-Year Record of Sulfur Dioxide and Ash Emissions

    NASA Astrophysics Data System (ADS)

    Carn, S. A.; Krueger, A. J.; Bluth, G. J.; Schaefer, S. J.; Krotkov, N. A.; Watson, I. M.; Datta, S.

    2002-05-01

    Since their first deployment in November 1978, the Total Ozone Mapping Spectrometer (TOMS) instruments have provided a unique, robust and near-continuous record of sulfur dioxide (SO2) and ash emissions from active volcanoes worldwide. Data from the four TOMS satellites that have flown to date (Nimbus-7, Meteor-3, ADEOS and Earth Probe) have been incorporated into a TOMS volcanic emissions database that presently covers 22 years of SO2 and ash emissions, representing one of the longest satellite-derived records of volcanic activity in existence. At the beginning of 2002, this database comprised 194 individual eruptive events produced during 100 eruptions from 60 volcanoes, resulting in a total of 666 days of volcanic cloud observations by TOMS. Regular eruptions of the African volcano Nyamuragira (DR Congo) since 1978, accompanied by copious SO2 production (Guth et al., 2002), have alone contributed approximately 20% of the days on which clouds were observed. Indonesian volcanoes have produced over 30% of detected eruptive events, due largely to frequent explosive activity at Galunggung, Soputan and Colo during the 1980s. The latest SO2 retrieval results from Earth Probe (EP) TOMS document a period (1996-2001) lacking large explosive eruptions, and also dominated by SO2 emission from 4 eruptions of Nyamuragira. EP TOMS has detected the SO2 and ash produced during 39 eruptive events from 15 volcanoes to date, with volcanic clouds observed on 128 days. Data from EP TOMS have recently begun to degrade, and its erstwhile successor (QuikTOMS) failed to achieve orbit in 2001. New SO2 algorithms are currently being developed for the Ozone Monitoring Instrument (OMI), which will continue the TOMS record of UV remote sensing of volcanic emissions from 2004. OMI will offer SO2 detection limits up to 50 times lower than TOMS and comparable to COSPEC, offering the prospect of regular space-based measurement of passive degassing. Reference: A.L. Guth, G.J.S. Bluth & S.A. Carn

  4. Total toxicity equivalents emissions of SF6, CHF3, and CCl2F2 decomposed in a RF plasma environment.

    PubMed

    Wang, Ya-Fen; Shih, Minliang; Tsai, Cheng-Hsien; Tsai, Perng-Jy

    2006-03-01

    Sulfur hexafluorine compound (SF6), trifluoromethane (CHF3) and diclorodifluoromethane (CCl2F2) are extensively used in the semiconductor industry. They are global warming gases. Most studies have addressed the effective decomposition of fluorine compounds, rather than the toxicity of decomposed by-products. Hence, the concepts of toxicity equivalents (TEQs) were applied in this work. The results indicated that HF and SiF4 were the two greatest contributors of TEQ to the SF6/H2/Ar plasma system, while F2 and SiF4 were the two greatest contributors to the SF6/O2/Ar system. Additionally, SiF4 and HF were the two greatest contributors of TEQ to both the CHF3/H2/Ar and CHF3/O2/Ar plasma systems. HF and HCl were the two greatest contributors of TEQ to the CCl2F2/H2/Ar plasma system, and Cl2 and COCl2 were the two greatest contributors to the CCl2F2/O2/Ar system. HCl and HF can be recovered using wet scrubbing, which reduces the toxicity of these emission gases. Consequently, the hydrogen-based plasma system was a better alternative for treating gases that contained SF6, CHF3 and CCl2F2 from the TEQs point of view. PMID:16084562

  5. 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.

  6. India Co2 Emissions

    NASA Astrophysics Data System (ADS)

    Sharan, S.; Diffenbaugh, N. S.

    2010-12-01

    Is there a way to find a balance between improving living conditions for the people on the margins and also reducing emissions while limiting our negative impacts on the climate? This is a critical question today because there are many arguments between developed and developing countries about who is responsible for global warming. Developed countries believe that it is the poor countries because they are not educated enough to know about how they are affecting the climate. While the developing countries hold wealthy nations responsible because they are using the most resources. However it is important to acknowledge the fact that if there was no gap in between the developed and developing countries our emissions total would be much higher. This “gap” has been a natural controlling factor in climate change. This is why I wanted to see if I could plot what it would look like if a developing country such as India were to produce emissions that the US or Switzerland or Norway are producing as developed countries. India has a population total of 1.1 billion compared to the US with only 298 million, Switzerland with 7.5 million, and Norway with 4.6 million people. When the population is compared to the emissions output in metric tons, per capita, India produced the least emissions out of these countries, 1.4 tons per person while having the second largest population in the world, while the US produced 19 tons per capita, Switzerland produced 5.6 and Norway produced 8.7 tons per capita in 2006. The emissions rate is growing every year and increases widely and globally. If India was producing emissions that equal Norway, Switzerland and the US the total emissions it would be producing annually would be 9 billion for Norway, 6 billion for Switzerland and 20 billion emissions for the US, all in the year 2006 alone. This shows how the balance between countries with huge populations and very little emission output and average population and high emission out put has

  7. 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

  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.

  9. Integrated emissions control system for residential CWS furnace. Annual status report number 1, 20 September 1989--30 September 1990

    SciTech Connect

    Balsavich, J.C.; Breault, R.W.

    1990-10-01

    One of the major obstacles to the successful development and commercialization of a coal-fired residential furnace is the need for a reliable, cost-effective emission control system. Tecogen Inc. is developing a novel, integrated emission control system to control NO{sub x}, SO{sub 2}, and particulate emissions. A reactor provides high sorbent particle residence time within the reactor to control SO{sub 2} emissions, while providing a means of extracting a substantial amount of the particulates present in the combustion gases. Final cleanup of any flyash exiting the reactor is completed with the use of high-efficiency bag filters. Tecogen Inc. developed a residential-scale Coal Water Slurry (CWS) combustor which makes use of centrifugal forces to separate and confine larger unburned coal particles in the furnace upper chamber. Various partitions are used to retard the axial, downward flow of these particles, and thus maximize their residence time in the hottest section of the combustor. By operating this combustor under staged conditions, the local stoichiometry in the primary zone can be controlled to minimize NO{sub x} emissions. During the first year of the program, work encompassed a literature search, developing an analytical model of the SO{sub 2} reactor, fabricating and assembling the initial prototype components, testing the prototype component, and estimating the operating and manufacturing costs.

  10. 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.

  11. 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.

  12. 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

  13. 40 CFR 98.33 - Calculating GHG emissions.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 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...

  14. 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.

  15. Effects of total CH 4/Ar gas pressure on the structures and field electron emission properties of carbon nanomaterials grown by plasma-enhanced chemical vapor deposition

    NASA Astrophysics Data System (ADS)

    Qi, J. L.; Wang, X.; Zheng, W. T.; Tian, H. W.; Liu, C.; Lu, Y. L.; Peng, Y. S.; Cheng, G.

    2009-12-01

    The effects of total CH 4/Ar gas pressure on the growth of carbon nanomaterials on Si (1 0 0) substrate covered with CoO nanoparticles, using plasma-enhanced chemical vapor deposition (PECVD), were investigated. The structures of obtained products were correlated with the total gas pressure and changed from pure carbon nanotubes (CNTs) through hybrid CNTs/graphene sheets (GSs), to pure GSs as the total gas pressure changed from 20 to 4 Torr. The total gas pressure influenced the density of hydrogen radicals and Ar ions in chamber, which in turn determined the degree of how CoO nanoparticles were deoxidized and ion bombardment energy that governed the final carbon nanomaterials. Moreover, the obtained hybrid CNTs/GSs exhibited a lower turn-on field (1.4 V/μm) emission, compared to either 2.7 V/μm for pure CNTs or 2.2 V/μm for pure GSs, at current density of 10 μA/cm 2.

  16. Springtime carbon emission episodes at the Gosan background site revealed by total carbon, stable carbon isotopic composition, and thermal characteristics of carbonaceous particles

    NASA Astrophysics Data System (ADS)

    Jung, J.; Kawamura, K.

    2011-11-01

    In order to investigate the emission of carbonaceous aerosols at the Gosan background super-site (33.17° N, 126.10° E) in East Asia, total suspended particles (TSP) were collected during spring of 2007 and 2008 and analyzed for particulate organic carbon, elemental carbon, total carbon (TC), total nitrogen (TN), and stable carbon isotopic composition (δ13C) of TC. The stable carbon isotopic composition of TC (δ13CTC) was found to be lowest during pollen emission episodes (range: -26.2‰ to -23.5‰, avg. -25.2 ± 0.9‰), approaching those of the airborne pollen (-28.0‰) collected at the Gosan site. Based on a carbon isotope mass balance equation, we found that ~42% of TC in the TSP samples during the pollen episodes was attributed to airborne pollen from Japanese cedar trees planted around tangerine farms in Jeju Island. A negative correlation between the citric acid-carbon/TC ratios and δ13CTC was obtained during the pollen episodes. These results suggest that citric acid emitted from tangerine fruit may be adsorbed on the airborne pollen and then transported to the Gosan site. Thermal evolution patterns of organic carbon during the pollen episodes were characterized by high OC evolution in the OC2 temperature step (450 °C). Since thermal evolution patterns of organic aerosols are highly influenced by their molecular weight, they can be used as additional information on the formation of secondary organic aerosols and the effect of aging of organic aerosols during the long-range atmospheric transport and sources of organic aerosols.

  17. On-line determination of Sb(III) and total Sb using baker's yeast immobilized on polyurethane foam and hydride generation inductively coupled plasma optical emission spectrometry

    NASA Astrophysics Data System (ADS)

    Menegário, Amauri A.; Silva, Ariovaldo José; Pozzi, Eloísa; Durrant, Steven F.; Abreu, Cassio H.

    2006-09-01

    The yeast Saccharomyces cerevisiae was immobilized in cubes of polyurethane foam and the ability of this immobilized material to separate Sb(III) and Sb(V) was investigated. A method based on sequential determination of total Sb (after on-line reduction of Sb(V) to Sb(III) with thiourea) and Sb(III) (after on-line solid-liquid phase extraction) by hydride generation inductively coupled plasma optical emission spectrometry is proposed. A flow system assembled with solenoid valves was used to manage all stages of the process. The effects of pH, sample loading and elution flow rates on solid-liquid phase extraction of Sb(III) were evaluated. Also, the parameters related to on-line pre-reduction (reaction coil and flow rates) were optimized. Detection limits of 0.8 and 0.15 μg L - 1 were obtained for total Sb and Sb(III), respectively. The proposed method was applied to the analysis of river water and effluent samples. The results obtained for the determination of total Sb were in agreement with expected values, including the river water Standard Reference Material 1640 certified by the National Institute of Standards and Technology (NIST). Recoveries of Sb(III) and Sb(V) in spiked samples were between 81 ± 19 and 111 ±15% when 120 s of sample loading were used.

  18. 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.'

  19. 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.

  20. 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.

  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.

  2. 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.

  3. 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.

  4. 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.

  5. 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

  6. 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...

  7. Analysis of dilute aqueous multifluorophoric mixtures using excitation-emission matrix fluorescence (EEMF) and total synchronous fluorescence (TSF) spectroscopy: a comparative evaluation.

    PubMed

    Kumar, Keshav; Mishra, Ashok Kumar

    2013-12-15

    Excitation-emission matrix fluorescence (EEMF) and total synchronous fluorescence (TSF) spectroscopy are two conceptually different fluorescence techniques that have been used to map the fluorescence responses of the fluorophores present in a multifluorophoric mixture. EEMF was introduced four decades back and most of the fluorimeters have the suitable computer program which allows the acquisition EEMF spectra. Recently introduced TSF spectroscopy has been shown to possess good application potential in analytical fluorimetry and has started attracting the attention of analytical chemists. TSF data structure, however, is intrinsically different from EEMF data structure and a better understanding of TSF data structure is crucial to utilising its application potential. In the present work, a comprehensive comparative study between EEMF and TSF spectroscopic data set was performed by taking aqueous mixtures containing low concentrations of benzo[a]pyrene, chrysene, and pyrene as test case. The EEMF and TSF data structures were clearly explained by taking pyrene as an example. The effects of Rayleigh and Raman scattering on the quality of EEMF and TSF data sets were studied. EEMF and TSF data sets of dilute aqueous mixtures of benzo[a]pyrene, chrysene, and pyrene were subjected to three chemometric techniques PARAFAC, N-PLS, and MCR-ALS analysis. TSF data set in particular was found to be highly attuned to MCR-ALS analysis. Obtained results of chemometric analyses on EEMF and TSF data sets show that TSF data of dilute aqueous mixtures provides more accurate spectral and concentration information than EEMF data sets. Therefore, TSF spectroscopy could be considered as an alternate to the EEMF for the analyses of dilute multifluorophoric mixtures.

  8. 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.

  9. 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.

  10. 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.

  11. The impact of residential combustion emission on Arctic aerosol concentrations

    NASA Astrophysics Data System (ADS)

    Eckhardt, Sabine; Stohl, Andreas; Olivie, Dirk J. L.; Grini, Alf

    2016-04-01

    Arctic haze is a seasonal phenomenon with high concentrations of accumulation-mode aerosols occurring in the Arctic in winter and early spring. It has been challenging to reproduced this cylce and concentration levels with atmospheric transport and climate models. However, simulations have been improving recently and it has been shown, that a better scavenging parametrization as well as more realistic emissions are important to obtain better results. In this study we focus on the emission from residential heating, which depend on air temperature, as heating demand is higher on cold days. Varying this emission shows a clear effect on modeled Arctic concentrations. Arctic-mean and annual-mean concentrations of black carbon from Arctic domestic combustion emissions due to heating requirements, are nearly 70% higher when accounting for diurnal emission variability relative to constant emissions (Stohl et al., 2013). Emissions are high when ambient temperatures are low and cold air is transported to the Arctic. In order to capture this systematic effect, we created an interactive emission module for NorESM, a climate model, using the heating degree-day concept. Domestic combustion emissions of BC and other species are scaled interactively with the modeled ambient air temperatures, while securing that levels of annual total emissions from emission scenarios are reproduced. We compare the modeled aerosol concentration in the Arctic to observations and show the level of improvements achieved by using varying emission.

  12. N2O Emissions From a Fertilized Grassland: Modeling and Measurements

    NASA Astrophysics Data System (ADS)

    Hsieh, C.

    2005-12-01

    N2O emissions from a fertilized grassland near Cork, Ireland were continuously measured during 2003 using the eddy covariance method. For most of the year N2O emissions were close to zero and the bulk of the emission occurred in only eight major events, each event lasting from two to twenty days. This data set was used to test the N2O emissions predicted by the DNDC (DeNitrification-DeComposition) model. Good agreement between measured and modeled N2O emissions was found, thus providing a basis for using the model to simulate (a) background N2O emissions and (b) the effect of future climate perturbations on N2O emissions. Our future climate projections are based on the standard Hadley Center model output of the IS92a scenario for Ireland in which the average temperature increases for the whole year and precipitation increases in winter but decreases in summer. The measured annual N2O emission was 11.6 kg N/ha. A total of 335 kg/ha of chemical and organic N was applied, giving an emission factor of 3.4%, uncorrected for background emission. Based on the DNDC model prediction with zero N applications, the background emission accounts for 15% of the total annual observed N2O emission. The DNDC model predicts that the future climate shifts based on the IS92a scenario will increase total annual N2O emission by 45% (7.0 kg N2O-N/ha). By comparison, a decrease of 10% in total N applications (in order to comply with EU water quality legislation) leads to a predicted reduction in current N2O emissions of only 7% (0.9 kg N2O-N/ha). Thus the projected increase in N2O emission caused by climate perturbations is far larger than the decrease expected from reduced fertilization to comply with water quality legislation.

  13. 40 CFR 98.33 - Calculating GHG emissions.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... chapter, as described in paragraph (a)(5) of this section. For units that combust both biomass and fossil... quarterly totals are summed to determine the annual CO2 mass emissions. (vii) If both biomass and fossil... paragraphs (a)(5)(i) through (a)(5)(iii) of this section, if both biomass and fossil fuel are...

  14. 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.

  15. 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.

  16. 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

  17. Road traffic emission factors for heavy metals

    NASA Astrophysics Data System (ADS)

    Johansson, Christer; Norman, Michael; Burman, Lars

    Quantifying the emissions and concentrations of heavy metals in urban air is a prerequisite for assessing their health effects. In this paper a combination of measurements and modelling is used to assess the contribution from road traffic emissions. Concentrations of particulate heavy metals in air were measured simultaneously during 1 year at a densely trafficked street and at an urban background site in Stockholm, Sweden. Annual mean concentrations of cadmium were 50 times lower than the EU directive and for nickel and arsenic concentrations were 10 and six times lower, respectively. More than a factor of two higher concentrations was in general observed at the street in comparison to roof levels indicating the strong influence from local road traffic emissions. The only compound with a significantly decreasing trend in the urban background was Pb with 9.1 ng m -3 in 1995/96 compared to 3.4 ng m -3 2003/04. This is likely due to decreased emissions from wear of brake linings and reduced emissions due to oil and coal combustion in central Europe. Total road traffic emission factors for heavy metals were estimated using parallel measurements of NOx concentrations and knowledge of NOx emission factors. In general, the emission factors for the street were higher than reported in road tunnel measurements. This could partly be due to different driving conditions, since especially for metals which are mainly emitted from brake wear, more stop and go driving in the street compared to in road tunnels is likely to increase emissions. Total emissions were compared with exhaust emissions, obtained from the COPERT model and brake wear emissions based on an earlier study in Stockholm. For Cu, Ni and Zn the sum of brake wear and exhaust emissions agreed very well with estimated total emission factors in this study. More than 90% of the road traffic emissions of Cu were due to brake wear. For Ni more than 80% is estimated to be due to exhaust emissions and for Zn around 40% of

  18. 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...

  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, 2014 CFR

    2014-07-01

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

  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

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

  1. Modeling total reduced sulfur and sulfur dioxide emissions from a kraft recovery boiler using an artificial neural network, and, Investigating volatile organic compounds in an urban intermountain valley using a TD/GC/MS methodology and intrinsic tracer molecules

    NASA Astrophysics Data System (ADS)

    Wrobel, Christopher Louis

    2000-11-01

    Back-propagation neural networks were trained to predict total reduced sulfur (TRS) and SO2 emissions from kraft recovery boiler operational data. A 0.721 coefficient of correlation was achieved between actual and predicted sulfur emissions on test data withheld from network training. The artificial neural network (ANN) models found an inverse, linear relationship between TRS/SO2 emissions and percent opacity. A number of relationships among operating parameters and sulfur emissions were identified by the ANN models. These relationships were used to formulate strategies for reducing sulfur emissions. Disagreement between ANN model predictions on a subsequent data set revealed an additional scenario for sulfur release not present in the training data. ANN modeling was demonstrated to be an effective tool for analyzing process variables when balancing productivity and environmental concerns. Five receptor sites distributed in the Missoula Valley, Montana, were employed to investigate possible VOC (benzene, 2,3,4-trimethylpentane, toluene, ethylbenzene, m-/p-xylene, o-xylene, naphthalene, acetone, chloroform, α-pinene, β-pinene, p-cymene and limonene) sources. The most dominant source of VOCs was found to be vehicle emissions. Furthermore, anthropogenic sources of terpenoids overwhelmed biogenic emissions, on a local scale. Difficulties correlating wind direction and pollutant levels could be explained by wind direction variability, low wind speed and seasonally dependent meteorological factors. Significant evidence was compiled to support the use of p-cymene as a tracer molecule for pulp mill VOC emissions. Apportionment techniques using o-xylene and p-cymene as tracers for automobile and pulp mill emissions, respectively, were employed to estimate each source's VOC contribution. Motor vehicles were estimated to contribute between 56 and 100 percent of the aromatic pollutants in the Missoula Valley airshed, depending upon the sampling location. Pulp mill emissions

  2. 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.

  3. 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.

  4. Total protein

    MedlinePlus

    ... page: //medlineplus.gov/ency/article/003483.htm Total protein To use the sharing features on this page, please enable JavaScript. The total protein test measures the total amount of two classes ...

  5. 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.

  6. 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

    ... and controlled organic HAP emissions from my wet-out area(s) and from my oven(s) for continuous lamination/casting operations? 63.5870 Section 63.5870 Protection of Environment ENVIRONMENTAL PROTECTION... uncontrolled and controlled organic HAP emissions from my wet-out area(s) and from my oven(s) for...

  7. 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

    ... factor is specific to the wet-out area only, or to the oven only, then you must develop the corresponding... 40 Protection of Environment 12 2010-07-01 2010-07-01 true How do I calculate annual uncontrolled... lamination/casting operations? 63.5870 Section 63.5870 Protection of Environment ENVIRONMENTAL...

  8. 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...

  9. 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

  10. 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.

  11. Estimation of methane and nitrous oxide emissions from Indian livestock.

    PubMed

    Patra, Amlan K

    2012-10-26

    Greenhouse gas (GHG; methane and nitrous oxide) emissions from enteric fermentation and manure management of Indian livestock were estimated from the last two Indian livestock census datasets (2003 and 2007) using IPCC Tier 2 (2006) guidelines. The total annual GHG emissions from Indian livestock increased in 2007 compared to the year 2003 with an annual growth rate of 1.52% over this period. The contributions of GHG by dairy cattle, non-dairy cattle, buffaloes, goats, sheep and other animals (yak, mithun, horse, donkeys, pigs and poultry) were 30.52, 24.0, 37.7, 4.34, 2.09 and 3.52%, respectively, in 2007. Enteric fermentation was the major source of methane, accounting for 89.2% of the total GHG emissions, followed by manure methane (9.49%). Nitrous oxide emissions accounted for 1.34%. GHG emissions (CO(2)-eq. per kg of fat and protein corrected milk (FPCM)) by female animals were considerably lower for crossbred cows (1161 g), followed by buffaloes (1332 g) and goats (2699 g), and were the highest for indigenous cattle (3261 g) in 2007. There was a decreasing trend in GHG emissions (-1.82% annual growth rate) in relation to milk production from 2003 to 2007 (1818 g and 1689 g CO(2)-eq. per kg FPCM in 2003 and 2007, respectively). This study revealed that GHG emissions (total as well as per unit of products) from dairy and other categories of livestock populations could be reduced substantially through proper dairy herd management without compromising animal production. In conclusion, although the total GHG emissions from Indian livestock increased in 2007, there was a decreasing trend in GHG production per kg of milk production or animal products.

  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. Estimating methane and nitrous oxide emissions in California using multi-tower observations and hierarchical Bayesian inversion

    NASA Astrophysics Data System (ADS)

    Jeong, S.; Hsu, Y.; Newman, S.; Zhang, J.; Andrews, A. E.; Bianco, L.; Bagley, J.; Cui, X.; Graven, H. D.; Kim, J.; Salameh, P.; LaFranchi, B. W.; Priest, C.; Campos-Pineda, M.; Novakovskaia, E.; Sloop, C.; Michelsen, H. A.; Bambha, R.; Weiss, R. F.; Keeling, R. F.; Fischer, M. L.

    2015-12-01

    We present an analysis of annual state total methane (CH4) and nitrous oxide (N2O) emissions from California using atmospheric observations from thirteen sites (six sites for N2O) in California during June 2013 - May 2014. A hierarchical Bayesian inversion (HBI) method is used to estimate CH4 and N2O emissions for spatial regions (0.3 degree pixels) by comparing measured mixing ratios with transport model (WRF-STILT) predictions. Using the multi-site measurements across California, the HBI analysis constrains a significant portion of expected emissions for both CH4 and N2O in the Central Valley and southern California. Based on the HBI analysis, we estimate a likely range of the state's annual CH4 emissions is 2.4 - 2.7 Tg CH4/yr (at 68% confidence), which is 1.4 - 1.6 times the total estimated by the California Air Resources Board (CARB). Similarly, we estimate the state's annual N2O emissions to be 77 - 95 Gg N2O/yr (at 68% confidence), which are 1.6 - 2.0 times CARB's state total. These results suggest that the combined total of CH4 and N2O emissions from the HBI analysis would comprise 18 - 21% of state total greenhouse gas (GHG) emissions, higher than 12% estimated in the current state inventory. Additionally, we expand previous evaluations of possible systematic bias in annual emission estimates due to transport model error by comparing measured and predicted carbon monoxide (CO) for four of the sites. These results highlight the need for multiple independent methods to estimate non-CO2 GHG emissions, and offer insight into opportunities for non-CO2 GHG emission mitigation efforts towards achieving California's GHG emission goals.

  15. 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.

  16. [Calculation of regional carbon emission: a case of Guangdong Province].

    PubMed

    Zhai, Shi-Yan; Wang, Zheng; Ma, Xiao-Zhe; Huang, Rui; Liu, Chang-Xin; Zhu, Yong-Bin

    2011-06-01

    By using IPCC carbon emission calculation formula (2006 edition), economy-carbon emission dynamic model, and cement carbon emission model, a regional carbon emission calculation framework was established, and, taking Guangdong Province as a case, its energy consumption carbon emission, cement production CO2 emission, and forest carbon sink values in 2008-2050 were predicted, based on the socio-economic statistical data, energy consumption data, cement production data, and forest carbon sink data of the Province. In 2008-2050, the cement production CO2 emission in the Province would be basically stable, with an annual carbon emission being 10-15 Mt C, the energy consumption carbon emission and the total carbon emission would be in inverse U-shape, with the peaks occurred in 2035 and 2036, respectively, and the carbon emission intensity would be decreased constantly while the forest carbon sink would have a fluctuated decline. It was feasible and reasonable to use the regional carbon emission calculation framework established in this paper to calculate the carbon emission in Guangdong Province. PMID:21941757

  17. 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.

  18. 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.

  19. LLNL NESHAP's 1999 Annual Report

    SciTech Connect

    Gallegos, G.; Biermann, A.H.; Harrach, R.J.; Bertoldo, N.A.; Berger, R.L.; Surano,K.A.

    2000-06-01

    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 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 1999 operations are summarized.

  20. 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.

  1. Comprehensive Black Carbon Emission Inventory of India: Uncertainty Analyses

    NASA Astrophysics Data System (ADS)

    Burkhart, J. F.; Paliwal, U.; Sharma, M.

    2015-12-01

    We present a new GIS based comprehensive high resolution grid wise emission inventory of Black carbon from India in the year 2011. The emissions have been determined at district level and were spatially distributed into grids at a resolution of 40x40 km2. The uncertainty in emissions has been estimated using Monte Carlo simulation by considering the variability in activity data and emission factors. Monthly variation of BC emissions has also been determined. The total BC annual emission for India in 2011 is determined to be 892.12 ± 151.53 Gg/yr. Domestic fuels contributed maximum (48%) followed by Industry (22%), Transport (17%), open burning (12%) and others (1%).

  2. 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.

  3. 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.

  4. 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

  5. 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.

  6. 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.

  7. 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

  8. The total nitrogen budget of the UK- amounts, controls and prognosis

    NASA Astrophysics Data System (ADS)

    Worrall, F.; Burt, T. P.; Howden, N. K.; Whelan, M.

    2011-12-01

    This study estimates the total annual nitrogen budget of the UK from 1990 to 2020. The following inputs of nitrogen are considered: inorganic fertilizer, atmospheric deposition; food and feed imports; and biological nitrogen fixation. The outputs considered include: atmospheric emissions (including to N2); direct losses of sewage and industrial effluent to the sea; fluvial losses at source; food and feed exports; and terrestrial and aquatic denitrification to N2. The study is the first to include in-stream losses and terrestrial denitrification to N2 into a national nitrogen budget: in so doing it does not have to assume the total budget is in balance following inter-annual changes. Unlike previous studies, this study is not limited to reactive nitrogen species. It is shown here that: i) Inputs of inorganic fertilizer declined significantly over the study period; atmospheric deposition showed no change and food and feed imports significantly increased. ii) Outputs of fluvial nitrogen rose significantly, but atmospheric emissions of N20 and NH3 declined dramatically, while dentrification to N2 remained steady. iii) The UK was a net source of total nitrogen in 1990 of 527 (±40%) ktonnes N/yr (22 kg N/ha/yr). By 2005, it was a net source of 172 (±106%) ktonnes N/yr (7 kg N/ha/yr). iv) The prognosis for the N budget of the UK to 2020 is critically dependent upon the future trends and trade-offs between atmospheric emissions and applications of inorganic fertilisers. If atmospheric emissions follow current trends then by 2020 the net sink of total N in the UK will be 44 ktonnes N/yr, if atmospheric emissions are restricted to current UK government emissions targets, then the UK will be a net source of Total N of 151 ktonnes N/yr as reductions in the application of inorganic fertiliser outstrip declines in atmospheric emissions.

  9. 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

  10. 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.

  11. Nuclear Medicine Annual, 1986

    SciTech Connect

    Freeman, L.M.; Weissmann, H.S.

    1986-01-01

    Nuclear Medicine Annual, l986 features state-of-the-art reports on the technical aspects and clinical applications of single-photon emission computed tomography, as well as on monoclonal antibodies for radioimmunoimaging and on receptorbinding radiopharmaceuticals. Also included is a review of magnetic resonance imaging of congenital cardiac abnormalities. Other contributions cover bone mineral measurements; skeletal scintigraphy of the hands and wrists; and radionuclide blood-pool imaging in the diagnosis of deep-vein thrombosis of the leg.

  12. Reduction of inherent mercury emissions in PC combustion. Semi-annual technical progress report No. 2, January 1, 1996--June 30, 1996

    SciTech Connect

    Kramlich, J.C.; Sliger, R.N.; Going, D.J.

    1996-08-19

    The 1990 Clean Air Act Amendments handed the utility industry a major challenge for the coming years. The legislation requires that the U.S. Environmental Protection Agency set emission standards for the 189 compounds or compound families identified in the act as air toxics. Evaluations by EPRI have identified 37 of these species as concerns in power generation. This research focuses on the air pollution control of mercury and rate limiting steps in mercury capture.

  13. 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.

  14. The contribution of soil biogenic NO and HONO emissions from a managed hyperarid ecosystem to the regional NOx emissions during growing season

    NASA Astrophysics Data System (ADS)

    Mamtimin, Buhalqem; Meixner, Franz X.; Behrendt, Thomas; Badawy, Moawad; Wagner, Thomas

    2016-08-01

    A study was carried out to understand the contributions of soil biogenic NO emissions from managed (fertilized and irrigated) hyperarid ecosystems in NW China to the regional NOx emissions during the growing season. Soil biogenic net potential NO fluxes were quantified by laboratory incubation of soil samples from the three dominating ecosystems (desert, cotton, and grape fields). Regional biogenic NO emissions were calculated bottom-up hourly for the entire growing season (April-September 2010) by considering corresponding land use, hourly data of soil temperature, gravimetric soil moisture, and fertilizer enhancement factors. The regional HONO emissions were estimated using the ratio of the optimum condition ((FN,opt(HONO) to FN,opt (NO)). Regional anthropogenic NOx emissions were calculated bottom-up from annual statistical data provided by regional and local government bureaus which have been downscaled to monthly value. Regional top-down emission estimates of NOx were derived on the monthly basis from satellite observations (OMI) of tropospheric vertical NO2 column densities and prescribed values of the tropospheric NOx lifetime. In order to compare the top-down and bottom-up emission estimates, all emission estimates were expressed in terms of mass of atomic nitrogen. Consequently, monthly top-down NOx emissions (total) were compared with monthly bottom-up NOx emissions (biogenic + anthropogenic) for the time of the satellite overpass (around 13:00 LT) with the consideration of the diurnal cycle of bottom-up estimates. Annual variation in total Tohsun Oasis NOx emissions is characterized by a strong peak in winter (December-February) and a secondary peak in summer (June-August). During summer, soil biogenic emissions were from equal to double that of related anthropogenic emissions, and grape soils were the main contributor to soil biogenic emissions, followed by cotton soils, while emissions from the desert were negligible. The top-down and bottom

  15. Temporal and spatial distribution of atmospheric antimony emission inventories from coal combustion in China.

    PubMed

    Tian, H Z; Zhao, D; He, M C; Wang, Y; Cheng, K

    2011-06-01

    A multiple-year inventory of atmospheric antimony (Sb) emissions from coal combustion in China for the period of 1980-2007 has been calculated for the first time. Specifically, the emission inventories of Sb from 30 provinces and 4 economic sectors (thermal power, industry, residential use, and others) are evaluated and analyzed in detail. It shows that the total Sb emissions released from coal combustion in China have increased from 133.19 t in 1980 to 546.67 t in 2007, at an annually average growth rate of 5.4%. The antimony emissions are largely emitted by industrial sector and thermal power generation sector, contributing 53.6% and 26.9% of the totals, respectively. At provincial level, the distribution of Sb emissions shows significant variation. Between 2005 and 2007, provinces always rank at the top five largest Sb emissions are: Guizhou, Hunan, Hebei, Shandong, and Anhui.

  16. 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

    . 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

  17. 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

  18. Seasonality of monoterpene emission potentials in Quercus ilex and Pinus pinea: Implications for regional VOC emissions modeling

    NASA Astrophysics Data System (ADS)

    Keenan, Trevor; Niinemets, ÜLo; Sabate, Santi; Gracia, Carlos; PeñUelas, Josep

    2009-11-01

    VOC emissions from terrestrial ecosystems provide one of the principal controls over oxidative photochemistry in the lower atmosphere and the resulting air pollution. Such atmospheric processes have strong seasonal cycles. Although similar seasonal cycles in VOC emissions from terrestrial ecosystems have been reported, regional emissions inventories generally omit the effect of seasonality on emissions. We compiled measurement data on seasonal variations in monoterpene emissions potentials for two evergreen species (Quercus ilex and Pinus pinea) and used these data to construct two contrasting seasonal response functions for the inclusion in monoterpene emission models. We included these responses in the Niinemets et al. model and compared simulation results to those of the MEGAN model, both with and without its predicted seasonality. The effect of seasonality on regional monoterpene emissions inventories for European Mediterranean forests dominated by these species was tested for both models, using the GOTILWA+ biosphere model platform. The consideration of seasonality in the Niinemets et al. model reduced total estimated annual monoterpene emissions by up to 65% in some regions, with largest reductions at lower latitudes. The MEGAN model demonstrated a much weaker seasonal response than that in the Niinemets et al. model, and did not capture the between species seasonality differences found in this study. Results suggest that previous regional model inventories based on one fixed emission factor likely overestimate regional emissions, and species-specific expressions of seasonality may be necessary. The consideration of seasonality both largely reduces monoterpene emissions estimates, and changes their expected seasonal distribution.

  19. 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.

  20. 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.

  1. Effect of climate, intra and inter-annual variability, on nutrients emission (C,N, P) in stream water: lessons from an agricultural long term observatory of the temperate zone

    NASA Astrophysics Data System (ADS)

    Gascuel-Odoux, Chantal; Remi, Dupas; Patrick, Durand; Ophélie, Fovet; Gerard, Gruau; Anne, Jaffrezic; Guillaume, Humbert; Philippe, Merot; Gu, Sen

    2016-04-01

    Agriculture greatly contributes to modify C, N and P cycles, particularly in animal breeding regions due to high inputs. Climatic conditions, intra and inter-annual variabilities, modify nutrient stream water emissions, acting in time on transfer and transformation, accumulation and mobilization processes, connecting and disconnecting in time different compartments (soil, riparian areas, groundwater). In agricultural catchments, nutrient perturbations are dominated by agricultural land use, and decoupling human activities and climate effects is far from easy. Climate change generally appears as a secondary driver compared to land use. If studied, generally only one nutrient is considered. Only long term, high frequency and multiple element data series can decouple these two drivers. The Kervidy-Naizin watershed belongs to the AgrHyS environmental research observatory (http://www6.inra.fr/ore_agrhys_eng), itself included in RBV (French catchment network of the CZO). On this catchment, 6 years of daily data on DOC, NO3, SRP, TP concentrations allow us to analyze the effect of seasonal and inter-annual climatic variabilities on water quality (C, N, P). Different papers have been published on the effect of climate on nitrate (Molenat et al, 2008), SRP and TP (Dupas et al, 2015) and DOC (Humbert et al, 2015). We will present first results comparing the effect of climate on these three major solute forms of C, N and P. While C and P dynamics are very close and controlled by fluctuation of water table downslope, i.e. in riparian areas, mobilizing C and P in time, nitrate dynamics is controlled by GW dynamics upslope acting as the major N reservoir. As example, the dryness conditions in summer appears a key factor of the C and P emissions in autumn. All the three solute forms interact when anoxic conditions are observed in riparian zones. These basic processes explain how climatic variability can influence and explain interactions between C, N and P emissions in stream

  2. Emission of polycyclic aromatic hydrocarbons in China by county

    SciTech Connect

    Yanxu Zhang; Shu Tao; Jun Cao; Raymond M. Coveney III

    2007-02-15

    Quantitative relationships among social, economic, and climate parameters, and energy consumption for Chinese provinces, provide data for regression models' estimated rates of energy consumption and emission of polycyclic aromatic hydrocarbons (PAHs) by county. A nonlinear model was used for domestic coal combustion with total population and annual mean temperature as independent variables. Linear regression models were utilized for all other types of fuel consumption. Monte Carlo simulation demonstrated that emission factors, rather than the regression modeling, constitute the main source of uncertainty in prediction. Models were validated using available energy data of several northern and southern counties of China from the literature. The total PAHs produced by each county is approximately equivalent to the sum of the total emission from energy, coke, and aluminum production. 25 refs., 8 figs.

  3. The temporal and spatial distribution of carbon dioxide emissions from fossil-fuel use in North America

    SciTech Connect

    Gregg, J; Losey, London M; Andres, Robert Joseph; Blasing, T J; Marland, Gregg

    2009-01-01

    Refinements in the spatial and temporal resolution of North American fossil-fuel carbon dioxide (CO{sub 2}) emissions provide additional information about anthropogenic aspects of the carbon cycle. In North America, the seasonal and spatial patterns are a distinctive component to characterizing anthropogenic carbon emissions. The pattern of fossil-fuel-based CO{sub 2} emissions on a monthly scale has greater temporal and spatial variability than the flux aggregated to the national annual level. For some areas, monthly emissions can vary by as much as 85% for some fuels when compared with monthly estimates based on a uniform temporal and spatial distribution. The United States accounts for the majority of North American fossil carbon emissions, and the amplitude of the seasonal flux in emissions in the United States is greater than the total mean monthly emissions in both Canada and Mexico. Nevertheless, Canada and Mexico have distinctive seasonal patterns as well. For the continent, emissions were aggregated on a 5{sup o} x 10{sup o} latitude-longitude grid. The monthly pattern of emissions varies on both a north-south and east-west gradient and evolves through the time period analyzed (1990-2007). For many areas in North America, the magnitude of the month-to-month variation is larger than the total annual emissions from land use change, making the characterization of emissions patterns essential to understanding humanity's influence on the carbon cycle.

  4. 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.

  5. 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.

  6. New estimates of direct N2O emissions from Chinese croplands from 1980 to 2007 using localized emission factors

    NASA Astrophysics Data System (ADS)

    Gao, B.; Ju, X. T.; Zhang, Q.; Christie, P.; Zhang, F. S.

    2011-07-01

    Nitrous oxide (N2O) is a long-lived greenhouse gas with a large radiation intensity and it is emitted mainly from agricultural land. Accurate estimates of total direct N2O emissions from croplands on a country scale are important for global budgets of anthropogenic sources of N2O emissions and for the development of effective mitigation strategies. The objectives of this study were to re-estimate direct N2O emissions using localized emission factors and a database of measurements from Chinese croplands. We obtained N2O emission factors for paddy fields (0.41 %) and uplands (1.05 %) from a normalization process through cube root transformation of the original data after comparing the results of normalization from the original values, logarithmic and cube root transformations because the frequency of the original data was not normally distributed. Direct N2O emissions from Chinese croplands from 1980 to 2007 were estimated using IPCC (2006) guidelines combined with separate localized emission factors for paddy fields and upland areas. Direct N2O emissions from paddy fields showed little change, increasing by 11 % with an annual rate of increase of 0.4 % from 29.8 Gg N2O-N in 1980 to 33.1 Gg N2O-N in 2007. In contrast, emissions from uplands changed dramatically, increasing by 296 % with an annual rate of 10.9 % from 64.4 Gg N2O-N in 1980 to 255.3 Gg N2O-N in 2007. Total direct N2O emissions from Chinese croplands increased by 206 % with an annual rate of 7.6 % from 94.2 Gg N2O-N in 1980 to 288.4 Gg N2O-N in 2007, and were determined mainly by upland emissions (accounting for 68.4-88.5 % of total emissions from 1980 to 2007). Synthetic nitrogen fertilizers played a major role in N2O emissions from agricultural land, and the magnitude of the contributions to total direct N2O emissions made by different amendments was synthetic N fertilizer > manure > straw, representing about 77, 16, and 6.5 % of total direct N2O emissions, respectively, between 2000 and 2007. The

  7. New estimates of direct N2O emissions from Chinese croplands from 1980 to 2007 using localized emission factors

    NASA Astrophysics Data System (ADS)

    Gao, B.; Ju, X. T.; Zhang, Q.; Christie, P.; Zhang, F. S.

    2011-10-01

    Nitrous oxide (N2O) is a long-lived greenhouse gas with a large radiation intensity and it is emitted mainly from agricultural land. Accurate estimates of total direct N2O emissions from croplands on a country scale are important for global budgets of anthropogenic sources of N2O emissions and for the development of effective mitigation strategies. The objectives of this study were to re-estimate direct N2O emissions using localized emission factors and a database of measurements from Chinese croplands. We obtained N2O emission factors for paddy fields (0.41 ± 0.04%) and uplands (1.05 ± 0.02%) from a normalization process through cube root transformation of the original data. After comparing the results of normalization from the original values, Logarithmic and cube root transformations were used because the frequency of the original data was not normally distributed. Direct N2O emissions from Chinese croplands from 1980 to 2007 were estimated using IPCC (2006) guidelines combined with separate localized emission factors for paddy fields and upland areas. Direct N2O emissions from paddy fields showed little change, increasing by 10.5% with an annual rate of increase of 0.4% from 32.3 Gg N2O-N in 1980 to 35.7 Gg N2O-N in 2007. In contrast, emissions from uplands changed dramatically, increasing by 308% with an annual rate of 11% from 68.0 Gg N2O-N in 1980 to 278 Gg N2O-N in 2007. Total direct N2O emissions from Chinese croplands increased by 213% with an annual rate of 7.6% from 100 Gg N2O-N in 1980 to 313 Gg N2O-N in 2007, and were determined mainly by upland emissions (accounting for 67.8-88.6% of total emissions from 1980 to 2007). Synthetic N fertilizers played a major role in N2O emissions from agricultural land, and the magnitude of the contributions to total direct N2O emissions made by different amendments was synthetic N fertilizer > manure > straw, representing about 78, 15, and 6% of total direct N2O emissions, respectively, between 2000 and 2007. The

  8. 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.

  9. 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...

  10. 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.

  11. 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

  12. Temporal and spatial distributions of total gaseous mercury concentrations in ambient air in a mountainous area in southwestern China: implications for industrial and domestic mercury emissions in remote areas in China.

    PubMed

    Fu, Xuewu; Feng, Xinbin; Wang, Shaofeng; Rothenberg, S; Shang, Lihai; Li, Zhonggen; Qiu, Guangle

    2009-03-15

    Spatial and temporal distributions of total gaseous mercury (TGM) concentrations in ambient air were investigated in the Mt. Gongga area (Sichuan province, PR China) from April 2006 to June 2007. The annual geometric mean TGM concentration at the Moxi baseline station was 3.90+/-1.20 ng m(-3). Geometric mean TGM concentrations at 14 representative sampling sites during the warm season ranged from 1.60 to 20.1 ng m(-3) and varied spatially, with levels decreasing between urbanized areas and more remote regions: urban area (U1-U3: 7.76+/-4.57 to 20.1+/-15.1 ng m(-3)), town (T1: 4.61+/-1.15 ng m(-3)) and village (V1-V4: 3.26+/-0.63 to 8.45+/-3.06 ng m(-3)), and remote area (R1-R6: 1.60+/-0.43 to 3.41+/-1.26 ng m(-3)). Our study suggested that industrial activities, especially non-ferrous smelting activities, were an important source of atmospheric Hg and played a vital role in the regional distribution of TGM. In addition, domestic coal and biomass combustion to heat residential homes were important sources of TGM in densely populated areas during the winter months.

  13. 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

  14. 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.

  15. 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

  16. 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.

  17. 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.

  18. 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.

  19. 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.

  20. Empirical model of global soil-biogenic NO{sub x} emissions

    SciTech Connect

    Yienger, J.J.; Levy, H. II

    1995-06-20

    The authors construct a global, temperature and precipitation dependent, empirical model of soil-biogenic NO{sub x} emissions using 6-hour general circulation model forcing. New features of this source relative to the latest published ones by Dignon et al. and Muller include synoptic-scale modeling of {open_quotes}pulsing{close_quotes} (the emissions burst following the wetting of a dry soil), a biome dependent scheme to estimate canopy recapture of NO{sub x}, and an explicit linear dependence of emission on N fertilizer rate for agricultural soils. Their best estimate for annual above-canopy emissions is 5.5 Tg N (NO{sub x}) with a range of 3.3-7.7 Tg N. Globally, the strongest emitters are agriculture, grasslands, and tropical rain forests, accounting for 41%, 35%, and 16% of the annual budget, respectively. {open_quotes}Pulsing{close_quotes} contributes 1.3 Tg N annually. In temperate regions, agriculture dominates emission, and in tropical regions, grassland dominates. Canopy recapture is significant, consuming, on average, possibly 50% of soil emissions. In temperate regions, periodic temperature changes associated with synoptic-scale disturbances can cause emission fluctuations of up to 20 ng N m{sup {minus}2}s{sup {minus}1}, indicating a close correlation between emission and warm weather events favorable to O{sub 3}/smog formation. By the year 2025, increasing use of nitrogen fertilizer may raise total annual emissions to 6.9 Tg N with agriculture accounting for more than 50% of the global source. Finally, biomass burning may add up to an additional 0.6 Tg N globally by stimulating emissions for a short period after the burn. 74 refs., 4 figs., 9 tabs.

  1. 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.

  2. [Estimation of VOC emission from forests in China based on the volume of tree species].

    PubMed

    Zhang, Gang-feng; Xie, Shao-dong

    2009-10-15

    Applying the volume data of dominant trees from statistics on the national forest resources, volatile organic compounds (VOC) emissions of each main tree species in China were estimated based on the light-temperature model put forward by Guenther. China's VOC emission inventory for forest was established, and the space-time and age-class distributions of VOC emission were analyzed. The results show that the total VOC emissions from forests in China are 8565.76 Gg, of which isoprene is 5689.38 Gg (66.42%), monoterpenes is 1343.95 Gg (15.69%), and other VOC is 1532.43 Gg (17.89%). VOC emissions have significant species variation. Quercus is the main species responsible for emission, contributing 45.22% of the total, followed by Picea and Pinus massoniana with 6.34% and 5.22%, respectively. Southwest and Northeast China are the major emission regions. In specific, Yunnan, Sichuan, Heilongjiang, Jilin and Shaanxi are the top five provinces producing the most VOC emissions from forests, and their contributions to the total are 15.09%, 12.58%, 10.35%, 7.49% and 7.37%, respectively. Emissions from these five provinces occupy more than half (52.88%) of the national emissions. Besides, VOC emissions show remarkable seasonal variation. Emissions in summer are the largest, accounting for 56.66% of the annual. Forests of different ages have different emission contribution. Half-mature forests play a key role and contribute 38.84% of the total emission from forests. PMID:19968092

  3. 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

  4. 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.

  5. LLNL NESHAPs 1998 annual report

    SciTech Connect

    Berger, R L; Bertoldo, N A; Biermann, A H; Gallegos, G; Hall, L C; Harrach, R J; Surano, K A

    1999-06-14

    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 (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 1998 operations are summarized here. (1) Livermore site: 0.055 mrem (0.55 {micro}Sv) (57% from point-source emissions, 43% from diffuse-source emissions). The point-source emissions include gaseous tritium modeled as tritiated water vapor as directed by EPA Region IX and is used for compliance purposes. LLNL believes a more realistic dose for the Livermore site is 0.049 mrem (0.49 {micro}Sv) (52% from point-source emissions, 48% from diffuse-source emissions). This dose is based on an assessment that represents a more realistic behavior of tritium gas in the environment. (2) Site 300: 0.024 mrem (0.24 {micro}Sv) (78% from point-source emissions, 22% 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.

  6. 40 CFR 61.123 - Emission testing.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... computing the emission rate for the test. The annual polonium-210 emission rate from a calciner or nodulizing kiln shall be determined by multiplying the measured polonium-210 emission rate in curies per Mg... operator changes his operation in such a way as to increase his emissions of polonium-210, such as...

  7. The Health Impacts of Energy Policy Pathways in Ulaanbaatar, Mongolia: A Total Exposure Assessment

    NASA Astrophysics Data System (ADS)

    Hill, L. A.; Damdinsuren, Y.; Olkhanud, P. B.; Smith, K. R.; Turner, J. R.; Edwards, R.; Odsuren, M.; Ochir, C.

    2015-12-01

    Ulaanbaatar is home to nearly half of Mongolia's 2.8 million residents. The city's rapid growth, frigid winters, valley topography, and reliance on coal-fired stoves have led to some of the worst winter pollution levels in the world. To better understand this issue, we modeled integrated PM2.5exposures and related health impacts for various city-wide heating policies through 2024. This assessment is one of the first to employ a total exposure approach and results of the 2014 Comparative Risk Assessments of the Global Burden of Disease Project (CRA/GBD) in a policy-relevant energy study. Emissions related to heating, traffic, and power generation were considered under Business as Usual, Moderate Improvement, and Max Improvement scenarios. Calibrated outdoor models were combined with indoor models, local infiltration and time activity estimates, and demographic projections to estimate PM2.5exposures in 2014 and 2024. Indoor exposures were assigned by heating type, home type, and smoking status; outdoor exposures were assigned through geocoding. Population average annual exposures were calculated and applied to local disease rates and integrated exposure-response curves (2014 CRA/GBD) to arrive at annual projections of premature deaths and DALYs. We estimate 2014 annual average exposures at 68 μg/m3, dictated almost exclusively by indoor winter exposures. Under current trends, annual exposures increase 10% to 75 μg/m3 in 2024. This is in stark contrast to the moderate and max improvement scenarios, which lead to 2024 annual exposures that are 31%, and 68% lower, respectively. Under the Moderate scenario, 2024 per capita annual DALY and death burdens drop 26% and 22%, respectively, from 2014 levels. Under the Max scenario, 2024 per capita annual DALY and death burdens drop 71% and 66%, respectively, from 2014. SHS becomes a major contributor as emissions from other sectors decrease. Reductions are dominated by cardiovascular and lower respiratory diseases in children.

  8. 12 CFR 1206.3 - Annual assessments.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... House Price Index (HPI) and the conforming loan limit; (13) Amounts deemed necessary by the Director to... 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...

  9. 12 CFR 1206.3 - Annual assessments.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... House Price Index (HPI) and the conforming loan limit; (13) Amounts deemed necessary by the Director to... 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...

  10. 12 CFR 1206.3 - Annual assessments.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... House Price Index (HPI) and the conforming loan limit; (13) Amounts deemed necessary by the Director to... 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...

  11. 12 CFR 1206.3 - Annual assessments.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... House Price Index (HPI) and the conforming loan limit; (13) Amounts deemed necessary by the Director to... 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...

  12. Proposal of new expanded selection criteria using total tumor size and 18F-fluorodeoxyglucose - positron emission tomography/computed tomography for living donor liver transplantation in patients with hepatocellular carcinoma: The National Cancer Center Korea criteria

    PubMed Central

    Lee, Seung Duk; Lee, Bora; Kim, Seong Hoon; Joo, Jungnam; Kim, Seok-Ki; Kim, Young-Kyu; Park, Sang-Jae

    2016-01-01

    AIM: To expand the living donor liver transplantation (LT) pool of eligible patients with hepatocellular carcinoma (HCC) using new morphological and biological criteria. METHODS: Patients with HCC who underwent living donor LT (LDLT) from March 2005 to May 2013 at the National Cancer Center Korea (NCCK) were enrolled. We performed the 18F-fluorodeoxyglucose positron emission tomography/computed tomography (PET/CT) before LDLT. Overall and disease-free survival analysis was done in patients to evaluate the usefulness of new NCCK criteria using PET/CT and total tumor size (10 cm). RESULTS: We enrolled a total of 280 patients who pathologically confirmed to have HCC and performed the PET/CT before transplantation. Among them, 164 (58.6%) patients fulfilled the NCCK criteria and 132 patients (47.1%) met the Milan criteria. Five-year overall and disease-free survival rates for patients who fulfilled the NCCK criteria showed 85.2% and 84.0%, respectively, and were significantly higher than those beyond the NCCK criteria (60.2% and 44.4%, respectively; P < 0.001). The correlation analysis between preoperative imaging tests and pathologic reports using Cohen’s Kappa demonstrated the better results in the NCCK criteria than those in the Milan criteria (0.850 vs 0.583). The comparison of disease-free analysis among the NCCK, Milan, and University of California, San Francisco (UCSF) criteria using the receiver operating characteristics curves revealed the similar area under the curve value criteria (NCCK vs Milan, P = 0.484; NCCK vs UCSF, P = 0.189 at 5-years). CONCLUSION: The NCCK criteria using hybrid concept of both morphological and biological parameters showed an excellent agreement between preoperative imaging and pathological results, and favorable survival outcomes. These new criteria might select the optimal patients with HCC waiting LDLT and expand the selection pool. PMID:27358787

  13. 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.

  14. De-excitation dynamics of Rydberg states in O2: I. Total cross sections for O I fluorescence emission following predissociation of 2σ- 1u(c4Σ- u)nσg3Σ-u states

    NASA Astrophysics Data System (ADS)

    Liebel, H.; Ehresmann, A.; Schmoranzer, H.; Demekhin, Ph V.; Lagutin, B. M.; Sukhorukov, V. L.

    2002-02-01

    Absolute cross sections for the total fluorescence emission between 97 and 131 nm by atomic oxygen formed after the photoexcitation of 2σ-1u(c4Σ- u)nσg3Σ- u Rydberg states in O2 and their successive predissociation were measured for the first time. The dissociation lifetimes and fluorescence yields were estimated using a stepwise model and the potential curve of the O2+2σ- 1u(c4Σ-u) state known from Beebe et al (Beebe N H F, Thulstrup E W and Andersen A 1976 J. Chem. Phys. 64 2080). The calculated lifetimes of the vibrational levels v = 0 and 1 of the 2σ-1u(c4Σ- u) state are 3.4×10-12 and 6.3×10-14 s, respectively. They agree with the measured data of Evans et al (Evans M, Stimson S, Ng C Y and Hsu C-W 1998 J. Chem. Phys. 109 1285) and are consistent with the results of the present experiment. The calculated lifetimes support the model of `fast' dissociation of the O2+2σ- 1u(c4Σ-u), v states in contrast to the earlier model of `slow' dissociation of Tanaka and Yoshimine (Tanaka K and Yoshimine M 1979 J. Chem. Phys. 70 1626).

  15. 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

  16. 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

  17. 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.

  18. The socioeconomic drivers of China’s 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 China’s 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.

  19. Estimating CH4 and N2O Emissions Using Tower Measurements in California

    NASA Astrophysics Data System (ADS)

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

    2011-12-01

    Based on an inverse modeling approach, we report spatio-temporally-resolved emissions for major non-CO2 greenhouse gases (CH4 and N2O) in California's Central Valley using measurements from a collaborative tower network. This large dataset, for the first time, allows quantification of the seasonal and inter-annual variations in California emissions, facilitating validation of uncertain state-wide annual emission totals that will be subject to future regulation by AB-32. Seasonally varying regional methane emissions (~100km) are estimated by scaling high-resolution (10-km scale) CH4 emission maps (initially tied to estimated state totals) for major known sources using a Bayesian inversion model to provide optimal agreement with aggregate mixing ratio data measured at the CARB-CEC-LBNL-NOAA 5-tower network. Two years of continuous CH4 measurements from the Walnut Grove (WGC) tall-tower indicate that annual CH4 emissions north of WGC (the southern end of the Sacramento Valley) are 2 - 3 times greater than the un-scaled inventory, with stronger summertime emissions that are likely driven by agriculture. South of WGC (in the Northern San Joaquin Valley) emissions are 0.9 - 1.5 times greater than the un-scaled inventory with small seasonal variation, where dairy emissions are expected to be dominant. Preliminary measurements from the 5-tower network suggest that long term data collected from those sites will greatly increase the ability to quantify and apportion CH4 emissions at 50 - 100 km scales over the entire Valley. Two years of daily N2O flask measurements from WGC indicate that N2O emissions are 2 - 3 times higher than the EDGAR3.2 emission inventory in Central California. Applying these scaling factors to the remainder of the California landscape suggests that total non-CO2 GHG's constitute 15 - 25% of California's total GHG emissions, and hence that mitigation of non-CO2 GHG emissions could meaningfully reduce California's overall GHG burden.

  20. 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...

  1. 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...

  2. 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...

  3. 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...

  4. 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...

  5. 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

  6. 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

  7. 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.

  8. Frozen cropland soil in northeast China as source of N2O and CO2 emissions.

    PubMed

    Miao, Shujie; Qiao, Yunfa; Han, Xiaozeng; Brancher Franco, Roberta; Burger, Martin

    2014-01-01

    Agricultural soils are important sources of atmospheric N2O and CO2. However, in boreal agro-ecosystems the contribution of the winter season to annual emissions of these gases has rarely been determined. In this study, soil N2O and CO2 fluxes were measured for 6 years in a corn-soybean-wheat rotation in northeast China to quantify the contribution of wintertime N2O and CO2 fluxes to annual emissions. The treatments were chemical fertilizer (NPK), chemical fertilizer plus composted pig manure (NPKOM), and control (Cont.). Mean soil N2O fluxes among all three treatments in the winter (November-March), when soil temperatures are below -7°C for extended periods, were 0.89-3.01 µg N m(-2) h(-1), and in between the growing season and winter (October and April), when freeze-thaw events occur, 1.73-5.48 µg N m(-2) h(-1). The cumulative N2O emissions were on average 0.27-1.39, 0.03-0.08 and 0.03-0.11 kg N2O_N ha(-1) during the growing season, October and April, and winter, respectively. The average contributions of winter N2O efflux to annual emissions were 6.3-12.1%. In all three seasons, the highest N2O emissions occurred in NPKOM, while NPK and Cont. emissions were similar. Cumulative CO2 emissions were 2.73-4.94, 0.13-0.20 and 0.07-0.11 Mg CO2-C ha(-1) during growing season, October and April, and winter, respectively. The contribution of winter CO2 to total annual emissions was 2.0-2.4%. Our results indicate that in boreal agricultural systems in northeast China, CO2 and N2O emissions continue throughout the winter. PMID:25536036

  9. Seasonal methane emissions by diffusion and ebullition from oligohaline marsh environments in coastal Louisiana

    USGS Publications Warehouse

    Leventhal, Joel S.; Guntenspergen, Glenn R.

    2004-01-01

    Methane is an important atmospheric greenhouse gas that is emitted from many natural and anthropogenic sources. In order to evaluate the global methane budget, precise data are needed from the diverse sources including coastal wetlands. Over 100 time-series determinations of methane emissions from an oligohaline wetland (brackish marsh) in coastal Louisiana show large variability during five seasonal sampling periods. Emission by both diffusion and ebullition (bubbles) was measured, however, neither of these emission modes were strongly dependent on either water depth or temperature (except in winter). Methane emission to static collectors placed over plants (Scirpus olneyi andSpartina patens) was not significantly different from shallow open water or mud. However, considerable heterogeneity in methane emissions and processes occurs even at a single site. Thus, establishing a reasonable estimate of the overall methane emission for a particular marsh environment and season requires multiple measurements at several sites. The average emissions for April, May, July, and September ranged from 31 to 54 mg/m2/h (744–1296 mg/m2/day). This can be separated into emissions from diffusion ranging from 8.3 to 20 mg/m2/h (18–50% of total) and emissions due to ebullition of 20–44 mg/m /h (50–82%). January emissions were much lower, amounting to 0.2 mg/m2/h (6 mg/m2/day), mainly by diffusion with only one episode of ebullition. Extrapolating these data to annual emissions gives total annual methane emissions of 203 g/m2/yr (61 g/m2/yr by diffusion and 142 g/m2/yr by ebullition).

  10. A global catalogue of large SO2 sources and emissions derived from the Ozone Monitoring Instrument

    NASA Astrophysics Data System (ADS)

    Fioletov, Vitali E.; McLinden, Chris A.; Krotkov, Nickolay; Li, Can; Joiner, Joanna; Theys, Nicolas; Carn, Simon; Moran, Mike D.

    2016-09-01

    Sulfur dioxide (SO2) measurements from the Ozone Monitoring Instrument (OMI) satellite sensor processed with the new principal component analysis (PCA) algorithm were used to detect large point emission sources or clusters of sources. The total of 491 continuously emitting point sources releasing from about 30 kt yr-1 to more than 4000 kt yr-1 of SO2 per year have been identified and grouped by country and by primary source origin: volcanoes (76 sources); power plants (297); smelters (53); and sources related to the oil and gas industry (65). The sources were identified using different methods, including through OMI measurements themselves applied to a new emission detection algorithm, and their evolution during the 2005-2014 period was traced by estimating annual emissions from each source. For volcanic sources, the study focused on continuous degassing, and emissions from explosive eruptions were excluded. Emissions from degassing volcanic sources were measured, many for the first time, and collectively they account for about 30 % of total SO2 emissions estimated from OMI measurements, but that fraction has increased in recent years given that cumulative global emissions from power plants and smelters are declining while emissions from oil and gas industry remained nearly constant. Anthropogenic emissions from the USA declined by 80 % over the 2005-2014 period as did emissions from western and central Europe, whereas emissions from India nearly doubled, and emissions from other large SO2-emitting regions (South Africa, Russia, Mexico, and the Middle East) remained fairly constant. In total, OMI-based estimates account for about a half of total reported anthropogenic SO2 emissions; the remaining half is likely related to sources emitting less than 30 kt yr-1 and not detected by OMI.

  11. 40 CFR 98.113 - Calculating GHG emissions.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... = Annual mass of alloy product k tapped from EAF (tons). Cproduct k = Carbon content in alloy product k... = Annual process CH4 emissions from an individual EAF (metric tons). Mproduct i = Annual mass of alloy.... EFproduct i = CH4 emission factor for alloy product i from Table K-1 in this subpart (kg of CH4...

  12. 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.

  13. 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

  14. 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

  15. Cold season emissions dominate the Arctic tundra methane budget

    NASA Astrophysics Data System (ADS)

    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.

  16. (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.

  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. 40 CFR 61.162 - Emission limits.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 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...

  19. 40 CFR 61.162 - Emission limits.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 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...

  20. 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...

  1. 40 CFR 61.162 - Emission limits.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 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...

  2. 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...

  3. Assessment of volatile organic compound emissions from ecosystems of China

    NASA Astrophysics Data System (ADS)

    Klinger, L. F.; Li, Q.-J.; Guenther, A. B.; Greenberg, J. P.; Baker, B.; Bai, J.-H.

    2002-11-01

    Isoprene, monoterpene, and other volatile organic compound (VOC) emissions from grasslands, shrublands, forests, and peatlands in China were characterized to estimate their regional magnitudes and to compare these emissions with those from landscapes of North America, Europe, and Africa. Ecological and VOC emission sampling was conducted at 52 sites centered in and around major research stations located in seven different regions of China: Inner Mongolia (temperate), Changbai Mountain (boreal-temperate), Beijing Mountain (temperate), Dinghu Mountain (subtropical), Ailao Mountain (subtropical), Kunming (subtropical), and Xishuangbanna (tropical). Transects were used to sample plant species and growth form composition, leafy (green) biomass, and leaf area in forests representing nearly all the major forest types of China. Leafy biomass was determined using generic algorithms based on tree diameter, canopy structure, and absolute cover. Measurements of VOC emissions were made on 386 of the 541 recorded species using a portable photo-ionization detector method. For 105 species, VOC emissions were also measured using a flow-through leaf cuvette sampling/gas chromatography analysis method. Results indicate that isoprene and monoterpene emissions, as well as leafy biomass, vary systematically along gradients of ecological succession in the same manner found in previous studies in the United States, Canada, and Africa. Applying these results to a regional VOC emissions model, we arrive at a value of 21 Tg C for total annual biogenic VOC emissions from China, compared to 5 Tg C of VOCs released annually from anthropogenic sources there. The isoprene and monoterpene emissions are nearly the same as those reported for Europe, which is comparable in size to China.

  4. 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.

  5. Lower Monoamine Oxidase-A Total Distribution Volume in Impulsive and Violent Male Offenders with Antisocial Personality Disorder and High Psychopathic Traits: An [11C] Harmine Positron Emission Tomography Study

    PubMed Central

    Kolla, Nathan J; Matthews, Brittany; Wilson, Alan A; Houle, Sylvain; Bagby, R Michael; Links, Paul; Simpson, Alexander I; Hussain, Amina; Meyer, Jeffrey H

    2016-01-01

    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 [11C] 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

  6. 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.

  7. Lower Monoamine Oxidase-A Total Distribution Volume in Impulsive and Violent Male Offenders with Antisocial Personality Disorder and High Psychopathic Traits: An [11C] Harmine Positron Emission Tomography Study

    PubMed Central

    Kolla, Nathan J; Matthews, Brittany; Wilson, Alan A; Houle, Sylvain; Michael Bagby, R; Links, Paul; Simpson, Alexander I; Hussain, Amina; Meyer, Jeffrey H

    2015-01-01

    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 [11C] 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

  8. 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

  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. 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

  11. 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.

  12. 40 CFR 98.113 - Calculating GHG emissions.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... must calculate and report the annual process CO2 emissions from each EAF not subject to paragraph (c... and report under this subpart the process CO2 emissions by operating and maintaining CEMS according to... subpart the annual process CO2 emissions using the procedure in either paragraph (b)(1) or (b)(2) of...

  13. 40 CFR 98.263 - Calculating GHG emissions.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... (CONTINUED) MANDATORY GREENHOUSE GAS REPORTING Phosphoric Acid Production § 98.263 Calculating GHG emissions. You must calculate and report the annual process CO2 emissions from each wet-process phosphoric acid... the annual CO2 mass emissions from each wet-process phosphoric acid process line using the methods...

  14. 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

  15. 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

  16. 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....”

  17. 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.

  18. 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.

  19. 21 CFR 1315.11 - Assessment of annual needs.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... QUOTAS FOR EPHEDRINE, PSEUDOEPHEDRINE, AND PHENYLPROPANOLAMINE Assessment of Annual Needs § 1315.11 Assessment of annual needs. (a) The Administrator shall determine the total quantity of ephedrine, pseudoephedrine, and phenylpropanolamine, including drug products containing ephedrine, pseudoephedrine,...

  20. 21 CFR 1315.11 - Assessment of annual needs.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... QUOTAS FOR EPHEDRINE, PSEUDOEPHEDRINE, AND PHENYLPROPANOLAMINE Assessment of Annual Needs § 1315.11 Assessment of annual needs. (a) The Administrator shall determine the total quantity of ephedrine, pseudoephedrine, and phenylpropanolamine, including drug products containing ephedrine, pseudoephedrine,...

  1. 21 CFR 1315.11 - Assessment of annual needs.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... QUOTAS FOR EPHEDRINE, PSEUDOEPHEDRINE, AND PHENYLPROPANOLAMINE Assessment of Annual Needs § 1315.11 Assessment of annual needs. (a) The Administrator shall determine the total quantity of ephedrine, pseudoephedrine, and phenylpropanolamine, including drug products containing ephedrine, pseudoephedrine,...

  2. 21 CFR 1315.11 - Assessment of annual needs.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... QUOTAS FOR EPHEDRINE, PSEUDOEPHEDRINE, AND PHENYLPROPANOLAMINE Assessment of Annual Needs § 1315.11 Assessment of annual needs. (a) The Administrator shall determine the total quantity of ephedrine, pseudoephedrine, and phenylpropanolamine, including drug products containing ephedrine, pseudoephedrine,...

  3. 21 CFR 1315.11 - Assessment of annual needs.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... QUOTAS FOR EPHEDRINE, PSEUDOEPHEDRINE, AND PHENYLPROPANOLAMINE Assessment of Annual Needs § 1315.11 Assessment of annual needs. (a) The Administrator shall determine the total quantity of ephedrine, pseudoephedrine, and phenylpropanolamine, including drug products containing ephedrine, pseudoephedrine,...

  4. 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.

  5. A multitower measurement network estimate of California's methane emissions

    SciTech Connect

    Jeong, Seongeun; Hsu, Ying-Kuang; Andrews, Arlyn E.; Bianco, Laura; Vaca, Patrick; Wilczak, James M.; Fischer, Marc L.

    2013-09-20

    In this paper, we 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). Finally, 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. Anthropogenic atmospheric nickel emissions and its distribution characteristics in China.

    PubMed

    Tian, H Z; Lu, L; Cheng, K; Hao, J M; Zhao, D; Wang, Y; Jia, W X; Qiu, P P

    2012-02-15

    Nickel and its compounds are considered as potential human carcinogens, and atmospheric nickel is one of the major routes for human exposure. By applying the best available fuel-based or product-based emission factors and annual activity levels, a multiple-year comprehensive inventory of anthropogenic atmospheric nickel emissions in China is presented with temporal trend and spatial resolutions for the period of 1980-2009 from both fuels combustion sources and industrial producing processes. We estimate that the total atmospheric nickel emissions from all the sources have increased from 1096.07 t in 1980 to 3933.71 t in 2009, at an average annual growth rate of 4.5%. Therein, coal combustion is the leading source, attributing 63.4% of the national total nickel emissions in 2009; liquid fuels consumption ranks the second, contributing 12.4% of the totals; biofuels burning accounts for 8.4% and the remaining sources together contribute 15.8% of the totals. Significant spatial variations are demonstrated among provincial emissions and the most concentrated regions are the highly industrialized and densely populated areas like the Yangtze River Delta, the Pearl River Delta and the Beijing-Tianjin-Hebei region. Moreover, the overall uncertainties are estimated at -32.6%-37.7% by using Monte Carlo simulation, most of which come from non-ferrous metals smelting category, implying the urgent need for further investigation and field tests. This article may help to combat the increasing stress on air heavy metals pollution in China and provide useful information to calculate global mass balance models for hazardous trace elements. PMID:22236636

  7. Anthropogenic atmospheric nickel emissions and its distribution characteristics in China.

    PubMed

    Tian, H Z; Lu, L; Cheng, K; Hao, J M; Zhao, D; Wang, Y; Jia, W X; Qiu, P P

    2012-02-15

    Nickel and its compounds are considered as potential human carcinogens, and atmospheric nickel is one of the major routes for human exposure. By applying the best available fuel-based or product-based emission factors and annual activity levels, a multiple-year comprehensive inventory of anthropogenic atmospheric nickel emissions in China is presented with temporal trend and spatial resolutions for the period of 1980-2009 from both fuels combustion sources and industrial producing processes. We estimate that the total atmospheric nickel emissions from all the sources have increased from 1096.07 t in 1980 to 3933.71 t in 2009, at an average annual growth rate of 4.5%. Therein, coal combustion is the leading source, attributing 63.4% of the national total nickel emissions in 2009; liquid fuels consumption ranks the second, contributing 12.4% of the totals; biofuels burning accounts for 8.4% and the remaining sources together contribute 15.8% of the totals. Significant spatial variations are demonstrated among provincial emissions and the most concentrated regions are the highly industrialized and densely populated areas like the Yangtze River Delta, the Pearl River Delta and the Beijing-Tianjin-Hebei region. Moreover, the overall uncertainties are estimated at -32.6%-37.7% by using Monte Carlo simulation, most of which come from non-ferrous metals smelting category, implying the urgent need for further investigation and field tests. This article may help to combat the increasing stress on air heavy metals pollution in China and provide useful information to calculate global mass balance models for hazardous trace elements.

  8. 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).

  9. 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.

  10. 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.

  11. Spatio-temporal variation of biogenic volatile organic compounds emissions in China.

    PubMed

    Li, L Y; Chen, Y; Xie, S D

    2013-11-01

    Aiming to reduce the large uncertainties of biogenic volatile organic compounds (BVOCs) emissions estimation, the emission inventory of BVOCs in China at a high spatial and temporal resolution of 36 km × 36 km and 1 h was established using MEGANv2.1 with MM5 providing high-resolution meteorological data, based on the most detailed and latest vegetation investigations. BVOC emissions from 82 plant functional types in China were computed firstly. More local species-specific emission rates were developed combining statistical analysis and category classification, and the leaf biomass was estimated based on vegetation volume and production with biomass-apportion models. The total annual BVOC emissions in 2003 were 42.5 Tg, including isoprene 23.4 Tg, monoterpene 5.6 Tg, sesquiterpene 1.0 Tg, and other VOCs (OVOCs) 12.5 Tg. Subtropical and tropical evergreen and deciduous broadleaf shrubs, Quercus, and bamboo contributed more than 45% to the total BVOC emissions. The highest biogenic emissions were found over northeastern, southeastern, and southwestern China. Strong seasonal pattern was observed with the highest BVOC emissions in July and the lowest in January and December, with daily emission peaked at approximately 13:00 or 14:00 local time. PMID:23916627

  12. 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.

  13. 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.

  14. 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.

  15. 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.

  16. 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.

  17. LLNL NESHAPs 2001 Annual Report

    SciTech Connect

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

    2002-06-18

    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 2001 are summarized here: (1) Livermore site: 0.017 mrem (0.17 {micro}Sv) (34% from point-source emissions, 66% 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: 0.054 mrem (0.54 {micro}Sv) (93% from point-source emissions, 7% 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.

  18. LLNL NESHAPs 2000 Annual Report

    SciTech Connect

    Gallegos, G M; Harrach, R J; Berger, R L; Bertoldo, N A; Tate, P J; Peterson, S R

    2001-06-01

    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 2000 operations are summarized here. {sm_bullet} Livermore site: 0.038 mrem (0.38 {micro}Sv) (45% from point-source emissions, 55% from diffuse-source emissions). The point-source emissions include gaseous tritium modeled as tritiated water vapor as directed by EPA Region IX, and the resulting dose is used for compliance purposes. {sm_bullet} Site 300: 0.019 mrem (0.19 {micro}Sv) (79% from point-source emissions, 21% from diffuse-source emissions). The EDEs were calculated using the EPA-approved CAP88-PC air dispersion/dose-assessment model, except for doses for four 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 input to CAP88-PC for each modeled source.

  19. Global mercury emissions from combustion in light of international fuel trading.

    PubMed

    Chen, Yilin; Wang, Rong; Shen, Huizhong; Li, Wei; Chen, Han; Huang, Ye; Zhang, Yanyan; Chen, Yuanchen; Su, Shu; Lin, Nan; Liu, Junfeng; Li, Bengang; Wang, Xilong; Liu, Wenxin; Coveney, Raymond M; Tao, Shu

    2014-01-01

    The spatially resolved emission inventory is essential for understanding the fate of mercury. Previous global mercury emission inventories for fuel combustion sources overlooked the influence of fuel trading on local emission estimates of many countries, mostly developing countries, for which national emission data are not available. This study demonstrates that in many countries, the mercury content of coal and petroleum locally consumed differ significantly from those locally produced. If the mercury content in locally produced fuels were used to estimate emission, then the resulting global mercury emissions from coal and petroleum would be overestimated by 4.7 and 72%, respectively. Even higher misestimations would exist in individual countries, leading to strong spatial bias. On the basis of the available data on fuel trading and an updated global fuel consumption database, a new mercury emission inventory for 64 combustion sources has been developed. The emissions were mapped at 0.1° × 0.1° resolution for 2007 and at country resolution for a period from 1960 to 2006. The estimated global total mercury emission from all combustion sources (fossil fuel, biomass fuel, solid waste, and wildfires) in 2007 was 1454 Mg (1232-1691 Mg as interquartile range from Monte Carlo simulation), among which elementary mercury (Hg(0)), divalent gaseous mercury (Hg(2+)), and particulate mercury (Hg(p)) were 725, 548, and 181 Mg, respectively. The total emission from anthropogenic sources, excluding wildfires, was 1040 Mg (886-1248 Mg), with coal combustion contributing more than half. Globally, total annual anthropogenic mercury emission from combustion sources increased from 285 Mg (263-358 Mg) in 1960 to 1040 Mg (886-1248 Mg) in 2007, owing to an increased fuel consumption in developing countries. However, mercury emissions from developed countries have decreased since 2000.

  20. 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.

  1. 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...

  2. 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\\...

  3. 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...

  4. 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,...

  5. 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…

  6. 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.

  7. Potential methane emission from north-temperate lakes following ice melt

    USGS Publications Warehouse

    Michmerhuizen, C.M.; Striegl, R.G.; McDonald, M.E.

    1996-01-01

    Methane, a radiatively active 'greenhouse' gas, is emitted from lakes to the atmosphere throughout the open-water season. However, annual lake CH4 emissions calculated solely from open-water measurements that exclude the time of spring ice melt may substantially underestimate the lake CH4 source strength. We estimated potential spring CH4 emission at the time of ice melt for 19 lakes in northern Minnesota and Wisconsin. Lakes ranged in area from 2.7 to 57,300 ha and varied in littoral zone sediment type. Regression analyses indicated that lake area explained 38% of the variance in potential CH4 emission for relatively undisturbed lakes; as lake area increases potential CH4 emission per unit area decreases. Inclusion of a second term accounting for the presence or absence of soft organic-rich littoral-zone sediments explained 83% of the variance in potential spring CH4 emission. Total estimated spring CH4 emission for 1993 for all Minnesota lakes north of 45?? with areas ???4 ha was 1.5 x 108 mol CH4 assuming a 1 : 1 ratio of soft littoral sediment to hard littoral sediment lakes. Emission estimates ranged from 5.3 x 107 tool assuming no lakes have soft organic-rich littoral sediments to 4.5 x 108 mol assuming all lakes have soft organic-rich littoral sediments. This spring CH4 pulse may make up as much as 40% of the CH4 annually emitted to the atmosphere by small lakes.

  8. Methane and nitrous oxide emissions from three paddy rice based cultivation systems in Southwest China

    NASA Astrophysics Data System (ADS)

    Jiang, Changsheng; Wang, Yuesi; Zheng, Xunhua; Zhu, Bo; Huang, Yao; Hao, Qingju

    2006-05-01

    To understand methane (CH4) and nitrous oxide (N2O) emissions from permanently flooded rice paddy fields and to develop mitigation options, a field experiment was conducted in situ for two years (from late 2002 to early 2005) in three rice-based cultivation systems, which are a permanently flooded rice field cultivated with a single time and followed by a non-rice season (PF), a rice-wheat rotation system (RW) and a rice-rapeseed rotation system (RR) in a hilly area in Southwest China. The results showed that the total CH4 emissions from PF were 646.3±52.1 and 215.0±45.4 kg CH4 hm-2 during the rice-growing period and non-rice period, respectively. Both values were much lower than many previous reports from similar regions in Southwest China. The CH4 emissions in the rice-growing season were more intensive in PF, as compared to RW and RR. Only 33% of the total annual CH4 emission in PF occurred in the non-rice season, though the duration of this season is two times longer than the rice season. The annual mean N2O flux in PF was 4.5±0.6 kg N2O hm-2 yr-1. The N2O emission in the rice-growing season was also more intensive than in the non-rice season, with only 16% of the total annual emission occurring in the non-rice season. The amounts of N2O emission in PF were ignorable compared to the CH4 emission in terms of the global warming potential (GWP). Changing PF to RW or RR not only eliminated CH4 emissions in the non-rice season, but also substantially reduced the CH4 emission during the following rice-growing period (ca. 58%, P<0.05). However, this change in cultivation system substantially increased N2O emissions, especially in the non-rice season, by a factor of 3.7 to 4.5. On the 100-year horizon, the integrated GWP of total annual CH4 and N2O emissions satisfies PF≫RR≈RW. The GWP of PF is higher than that of RW and RR by a factor of 2.6 and 2.7, respectively. Of the total GWP of CH4 and N2O emissions, CH4 emission contributed to 93%, 65% and 59% in PF, RW

  9. 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

  10. Historical variations of biogenic volatile organic compound emission inventories in China, 1981-2003

    NASA Astrophysics Data System (ADS)

    Li, L. Y.; Xie, S. D.

    2014-10-01

    To evaluate the variations in temporal and spatial distribution of biogenic volatile organic compound (BVOC) emissions in China, historical BVOC emission inventories at a spatial resolution of 36 km × 36 km for the period of 1981-2003 were developed firstly. Based on the time-varying statistical data and Vegetation Atlas of China (1:1,000,000), emissions of isoprene, 37 monoterpenes, 32 sesquiterpenes, and other volatile organic compounds (OVOCs) were estimated using MEGANv2.1 driven by WRF model. Results show China's BVOC emissions had increased by 28.01% at an annual average rate of 1.27% from 37.89 Tg in 1981 to 48.50 Tg in 2003. Emissions of isoprene, monoterpenes, sesquiterpenes, and OVOCs had increased by 41.60%, 34.78%, 41.05%, and 4.89%, respectively. With fixed meteorological variables, the estimated BVOC emissions would increase by 19.25%, resulting from the increasing of vegetation biomass during the last 23 years. On average, isoprene, monoterpenes, sesquiterpenes, and OVOCs were responsible for 52.40%, 12.73%, 2.58%, and 32.29% of the national BVOC emissions, respectively. β-pinene and α-pinene, farnesene and caryophyllene were the largest contributors to the total monoterpene and sesquiterpene emissions, respectively. The highest emissions were found over northeastern, southeastern, southwestern China, Qinling Mountain, and Hainan and Taiwan provinces. The regions with high emissions had been expanding over the years, especially in the Changbai Mountain, southern China, and southwestern forest regions. The lowest emissions in southern China occurred in 1984-1988. Almost all the provinces had experienced increasing emissions, but their contributions to the national emissions differed significantly over the past 23 years. Yunnan, Guangxi, Heilongjiang, Jiangxi, Fujian, Guangdong, and Sichuan provinces always dominated the national BVOC emissions, excluding in 1977-1981, when the three northeastern provinces had relatively lower emissions.

  11. 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

  12. 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%.

  13. TOTAL MOLECULAR GAS MASSES OF z {approx} 3 LYMAN- BREAK GALAXIES: CO(J = 1 {yields} 0) EMISSION IN MS 1512-cB58 AND THE COSMIC EYE

    SciTech Connect

    Riechers, Dominik A.; Carilli, Christopher L.; Momjian, Emmanuel; Walter, Fabian

    2010-12-01

    We report the detection of CO(J = 1 {yields} 0) emission toward the lensed L {sup *} {sub UV} Lyman-break galaxies (LBGs) MS 1512-cB58 (z = 2.73) and the Cosmic Eye (z = 3.07), using the Expanded Very Large Array. The strength of the CO line emission reveals molecular gas reservoirs with masses of (4.6 {+-} 1.1) x 10{sup 8} ({mu}{sub L}/32){sup -1} ({alpha}{sub CO}/0.8) M {sub sun} and (9.3 {+-} 1.6) x 10{sup 8} ({mu}{sub L}/28){sup -1} ({alpha}{sub CO}/0.8) M {sub sun}, respectively. These observations suggest {approx}30%-40% larger gas reservoirs than previously estimated based on CO(J = 3 {yields} 2) observations due to subthermal excitation of the J = 3 line. These observations also suggest gas mass fractions of 0.46 {+-} 0.17 and 0.16 {+-} 0.06. The CO(J = 1 {yields} 0) emission in the Cosmic Eye is slightly resolved on scales of 4.''5 {+-} 1.''5, consistent with previous studies of nebular emission lines. This suggests that the molecular gas is associated with the most intensely star-forming regions seen in the ultraviolet (UV). We do not resolve the CO(J = 1 {yields} 0) emission in cB58 at {approx}2'' resolution, but find that the CO(J = 1 {yields} 0) emission is also consistent with the position of the UV-brightest emission peak. The gas masses, gas fractions, moderate CO line excitation, and star formation efficiencies in these galaxies are consistent with what is found in nearby luminous infrared galaxies. These observations thus currently represent the best constraints on the molecular gas content of 'ordinary' (i.e., {approx}L* {sub UV}) z {approx} 3 star-forming galaxies. Despite comparable star formation rates, the gas properties of these young LBGs seem to be different from the recently identified optical/infrared-selected high-z massive, gas-rich star-forming galaxies, which are more gas-rich and massive, but have lower star formation efficiencies, and presumably trace a different galaxy population.

  14. 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.

  15. Energy use and carbon dioxide emissions from cropland production in the United States, 1990-2004.

    PubMed

    Nelson, Richard G; Hellwinckel, Chad M; Brandt, Craig C; West, Tristram O; De La Torre Ugarte, Daniel G; Marland, Gregg

    2009-01-01

    Changes in cropland production and management influence energy consumption and emissions of CO(2) from fossil-fuel combustion. A method was developed to calculate on-site and off-site energy and CO(2) emissions for cropping practices in the United States 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 CO(2) emissions for cropping practices enable (i) the monitoring of energy and emissions with changes in land management and (ii) 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 U.S. croplands in 2004 ranged from 1.6 to 7.9 GJ ha(-1) yr(-1) and from 5.5 to 20.5 GJ ha(-1) yr(-1), respectively. On-site and total CO(2) emissions in 2004 ranged from 23 to 176 kg C ha(-1) yr(-1) and from 91 to 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 to 1297 PJ yr(-1) (Petajoule = 1 x 10(15) Joule) with associated total fossil CO(2) emissions ranging from 21.5 to 23.2 Tg C yr(-1) (Teragram = 1 x 10(12) gram). The annual proportion of on-site CO(2) to total CO(2) emissions changed depending on the diversity of crops planted. Adoption of reduced tillage practices in the United States from 1990 to 2004 resulted in a net fossil emissions reduction of 2.4 Tg C.

  16. Cow power: the energy and emissions benefits of converting manure to biogas

    NASA Astrophysics Data System (ADS)

    Cuéllar, 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 sources—manure and coal combustion—with 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

  17. 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...

  18. 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.

  19. Shifting emissions to low latitudes had a greater influence on global tropospheric ozone than changing emission magnitude, 1980-2010

    NASA Astrophysics Data System (ADS)

    Zhang, Y.; Cooper, O. R.; West, J. J.

    2015-12-01

    Global anthropogenic emissions of short-lived O3 precursors (NOx, NMVOCs and CO) have increased since 1980. These increases are greatest in developing countries (China and India), while emissions have generally decreased in North America and Europe. Consequently, emissions have shifted southwards. Modeling studies have shown that the tropospheric O3 burden and resulting radiative forcing are more sensitive to emission changes in the tropics and Southern Hemisphere than in other regions. Here we separate the influence of the change in the spatial distributions of short-lived global anthropogenic emissions from that of the change in the emission magnitude and the change in global CH4 between 1980 and 2010. We use the global CAM-chem model with 2008-2012 GEOS-5 meteorology for all simulations, neglecting possible effects of climate change. The global tropospheric O3 burden is estimated to have increased by 28.12 Tg from 1980 to 2010, with the largest increases over 30°S—30°N (17.93 Tg). Of the total O3 burden change, the influence of the change in the spatial distributions of emissions contributes 16.39 Tg, roughly double the effect of the change in emission magnitude (8.59 Tg) and of the global CH4 change (7.48 Tg). The three-month O3 season MDA8 surface O3 has decreased over the U.S. and Europe, and increased over East and South Asia from 1980 to 2010, mainly because of changes in the emission distributions. Significant increases in the zonal annual average O3 are modeled in the upper troposphere (500 to 150 hPa) between 15°N and 40°N. Upper tropospheric O3 also increases over the U.S. and Europe, despite peroxyacetyl nitrate (PAN) decreases in the middle to upper troposphere resulting from regional emission reductions. These upper tropospheric changes result from the change in the spatial distributions of emissions, with little from contributions from the changes in emissions magnitude or methane, and reflect the intercontinental transport of O3. We conclude

  20. Greenhouse Gas Emissions from Septic Systems in New York State.

    PubMed

    Truhlar, Allison M; Rahm, Brian G; Brooks, Rachael A; Nadeau, Sarah A; Makarsky, Erin T; Walter, M Todd

    2016-07-01

    Onsite septic systems use microbial processes to eliminate organic wastes and nutrients such as nitrogen; these processes can contribute to air pollution through the release of greenhouse gases (GHGs). Current USEPA estimates for septic system GHG emissions are based on one study conducted in north-central California and are limited to methane; therefore, the contribution of these systems to the overall GHG emission budget is unclear. This study quantified and compared septic system GHG emissions from the soil over leach fields and the roof vent, which are the most likely locations for gas emissions during normal septic system operation. At each of eight septic systems, we measured fluxes of CH, CO, and NO using a static chamber method. The roof vent released the majority of septic system gas emissions. In addition, the leach field was a significant source of NO fluxes. Comparisons between leach field and vent emissions suggest that biological processes in the leach field soil may influence the type and quantity of gas released. Overall, our results suggest that (i) revisions are needed in USEPA guidance (e.g., septic systems are not currently listed as a source of NO emissions) and (ii) similar studies representing a wider range of climatic and geographic settings are needed. The total vent, sand filter, and leach field GHG emissions were 0.17, 0.045, and 0.050 t CO-equivalents capita yr, respectively. In total, this represents about 1.5% of the annual carbon footprint of an individual living in the United States. PMID:27380062

  1. 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±3 kg CO(2,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.

  2. Soil respiration in a mixed temperate forest and its contribution to total ecosystem respiration.

    PubMed

    Curiel Yuste, J; Nagy, M; Janssens, I A; Carrara, A; Ceulemans, R

    2005-05-01

    Soil respiration (SR) was measured with an infrared gas analyzer in nine plots representative of the heterogeneous vegetation in a mixed coniferous-deciduous forest in the Belgian Campine region. Selected plots included the two most representative overstory species (Pinus sylvestris L. and Quercus robur L.) in combination with the most representative understory species of the forest. A model that includes temperature and water as the main controlling variables was fitted to the data. We found large spatial variability in SR among plots, with typically lower fluxes under the coniferous overstory than under the deciduous overstory (means of 4.8 +/- 0.4 and 8.8 +/- 0.5 Mg C ha(-1) year(-1), respectively). Total annual soil carbon (C) emissions were estimated by weighting fluxes from different types of vegetation according to their relative contribution to the footprint area of the eddy covariance flux measurement. The relative contribution of the two main tree species to the footprint-weighted total SR varied among seasons with the more abundant coniferous overstory contributing the most to total SR during most of the year. Nonetheless, during summer, the contribution of deciduous plots to total SR was disproportionally high because of the more pronounced seasonality of belowground metabolic activity. Net ecosystem carbon dioxide exchange was measured by eddy covariance, and we estimated total ecosystem respiration (TER) with footprint-constrained nighttime fluxes. Mean total annual SR and TER were 6.1 +/- 0.11 and 9.1 +/- 1.15 Mg C ha(-1) year(-1), respectively. The 95% confidence interval of the ratio of annual SR:TER ranged from 0.58 to 0.76, with a mean of 0.67. The contribution of SR to TER tended to vary seasonally, with minimum contributions during summer (less than 50% of TER) and maximum contributions during winter (about 94% of TER).

  3. High resolution mapping of total deposition of acidifying pollutants

    NASA Astrophysics Data System (ADS)

    de Vos, Thierri; Zhang, Leiming

    2012-09-01

    A framework has been developed to estimate dry and wet deposition over Southern Belgium for a variety of acidifying substances on a 5 × 5 km2 grid. Concentrations of different compounds in the atmosphere or in the precipitation are provided by the measurement networks (both stations and gauges) and are interpolated over Southern Belgium. Dry deposition velocities are calculated using local meteorology and land use information, following the approach described in Zhang et al. (2001, 2003). Local precipitation is provided by merged radar-gauge observations. This is the first high resolution framework for Southern Belgium computing both time- and space-dependent deposition, using a modified kriging interpolation method (for SO2 and NO2), as well as radar-based precipitation. Estimated dry and wet depositions are compared with long range transport (LRT) model results, based on the European emission inventories. Although a good agreement is observed between our results and LRT model results on the annual totals averaged over Southern Belgium, the extent of agreement for the spatial variability of the annual deposition differs significantly from one pollutant to another. This new framework provides consistent high resolution maps for several pollutants, while improving the mapping of dry and wet deposition in Southern Belgium, in order to assess critical loads exceedances.

  4. Three-North Shelter Forest Program contribution to long-term increasing trends of biogenic isoprene emissions in northern China

    NASA Astrophysics Data System (ADS)

    Zhang, Xiaodong; Huang, Tao; Zhang, Leiming; Shen, Yanjie; Zhao, Yuan; Gao, Hong; Mao, Xiaoxuan; Jia, Chenhui; Ma, Jianmin

    2016-06-01

    To assess the long-term trends of isoprene emissions in northern China and the impact of the Three-North Shelter Forest Program (TNRSF) on these trends, a database of historical biogenic isoprene emissions from 1982 to 2010 was developed for this region using a biogenic emission model for gases and aerosols. The total amount of the biogenic isoprene emissions during the 3 decades was 4.4 Tg in northern China and 1.6 Tg in the TNRSF, with annual emissions ranging from 132 000 to 176 000 t yr-1 and from 45 000 to 70 000 t yr-1, respectively, in the two regions. Isoprene emission fluxes have increased substantially in many areas of the TNRSF over the last 3 decades due to the growing trees and vegetation coverage, especially in the central north China region where the highest emission incline reached to 58 % from 1982 to 2010. Biogenic isoprene emissions produced from anthropogenic forests tended to surpass those produced from natural forests, such as boreal forests in northeastern China. The estimated isoprene emissions suggest that the TNRSF has altered the long-term emission trend in north China from a decreasing trend during 1982 to 2010 (slope = -0.533, R2 = 0.05) to an increasing trend for the same period of time (slope = 0.347, R2 = 0.014), providing strong evidence for the change in the emissions of biogenic volatile organic compounds (BVOCs) induced by the human activities on decadal or longer timescales.

  5. Global emissions of HFC-23 estimated to year 2015

    NASA Astrophysics Data System (ADS)

    McCulloch, A.; Lindley, A. A.

    HFC-23 (trifluoromethane, fluoroform, CHF 3) is a powerful greenhouse gas that is formed at the reactor stage of the manufacture of HCFC-22 (chlorodifluoromethane, CHClF 2). The amount formed depends on the conditions used in the manufacturing process and, for individual plants, lies between 1% and 4% of the production of HCFC-22. While it is possible to reduce the formation of HFC-23 by optimising process conditions, it is not possible to eliminate its production. This requires destruction, generally by thermal oxidation. Under the Kyoto Protocol, developed countries have obligations to reduce greenhouse gas emissions and, in the developing world, there are projects under the Clean Development Mechanism for the incineration of HFC-23 waste streams. These should lead to a reduction in average global emission factors relative to production of HCFC-22. We present estimates of global production of HCFC-22 up to the year 2015 and also the calculated range of emissions of HFC-23 that may be consequences of this. In terms of the effect on climate change, the atmospheric burden of HFC-23 accumulated from emissions is calculated to contribute between 0.1% and 0.2% of the radiative forcing of climate in 2015. Annual emissions of HFC-23 would be equivalent to between 284 and 28 million tonnes of CO 2 in that year, when total anthropogenic greenhouse gas emissions are predicted to lie between 46,000 million and 59,000 million tonnes of CO 2 equivalent.

  6. LLNL NESHAPs project 1997 annual report

    SciTech Connect

    Gallegos, G.M.

    1998-06-01

    NESHAP`s 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 ({mu}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 1997 operations were Livermore site. 0 097 mrem (0 97 {mu}Sv) (80% from point-source emissions), 20% from diffuse-source emissions), Site 300 0 014 mrem (O 14 {mu}Sv) (38% from point-source emissions, 62% 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.

  7. 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.

  8. Contribution from urban heating to China's 2020 goal of emission reduction.

    PubMed

    Wang, Li; Chen, Xia; Wang, Lu; Sun, Shufeng; Tong, Lige; Yue, Xianfang; Yin, Shaowu; Zheng, Lifang

    2011-06-01

    To reduce inhalable particle and SO(x) pollution from coal-based urban central heating (UCH), China has been vigorously developing natural gas-based UCH for years. The CO(2) emissions of UCH, having an average annual growth rate of 10.3%, accounted for 4.4% of China's total CO(2) emissions in 2009. This paper analyzes the feasibility of replacing UCH with heat pump heating (HPH) in China's climatic suitable regions and evaluates the corresponding potential for energy saving and emission reduction. Current strategy of replacing coal-based UCH with natural gas-based UCH is expected to decrease CO(2) emissions by 63.5%. However, the CO(2) emissions of HPH are 55.4% less than those of natural gas-based UCH. Replacing coal-based UCH with HPH is capable of decreasing CO(2) emissions by 83.7% and consequently decreases the CO(2) emissions per unit of gross domestic product (GDP) by 4.2% by 2020 compared with 2005 level. This contributes about 10.5% to China's 2020 CO(2) emission reduction target. For controlling environmental pollution and protecting ecological environment better, China should adjust its strategy for CO(2) emission reduction by shifting its attention from replacing coal-based UCH with natural gas-based UCH to popularizing HPH in climatic suitable regions.

  9. 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.

  10. High resolution of anthropogenic atmospheric emissions of 12 heavy metals in the three biggest metropolitan areas, China

    NASA Astrophysics Data System (ADS)

    Tian, H.; Zhu, C.

    2015-12-01

    Atmospheric emissions of typical toxic heavy metals from anthropogenic sources have received worldwide concerns due to their adverse effects on human health and the ecosystem. An integrated inventory of anthropogenic emissions of twelve HMs (Hg, As, Se, Pb, Cd, Cr, Ni, Sb, Mn, Co, Cu and Zn) in the three biggest metropolitan areas, including Beijing-Tianjin-Hebei (BTH) region, Yangtze River Delta (YRD) region and Pearl River Delta (PRD) region, are developed for 1980-2012 by combining with detailed activity data and inter-annual dynamic emission factors which are determined by S-shaped curves on account of technology progress, economic development, and emission control. The results indicate total emissions of twelve HMs in the three metropolitan regions have increased from 5448.8 tons in 1980 to 19054.9 tons in 2012, with an annual average growth rate of about 4.0%. Due to significant difference in industrial structures and energy consumption compositions, remarkable distinctions can be observed with respect to source contributions of total HM emissions from above three metropolitan areas. Specifically, the ferrous metal smelting sector, coal combustion by industrial boilers and coal combustion by power plants are found to be the primary source of total HM emissions in the BTH region (about 34.2%), YRD region (about 28.2%) and PRD region (about 24.3%), respectively. Furthermore, we allocate the annual emissions of these heavy metals in 2012 at a high spatial resolution of 9 km × 9 km grid with ArcGIS methodology and surrogate indexes, such as regional population and gross domestic product (GDP). The peak of HM emissions are mainly distributed over the grid cells of Beijing, Tianjin, Tangshan, Shijiazhuang, Handan and Baoding in the BTH region; Shanghai, Suzhou, Wuxi, Nanjing, Hangzhou, Ningbo in the YRD region; Guangzhou, Shenzhen, Dongguan, Foshan in the PYD region, respectively. Additionally, monthly emission profiles are established in order to further identify

  11. [Lead emission amount from coal combustion and its environment effect in Xi'an City].

    PubMed

    Luo, Kunli; Wang, Douhu; Tan, Jianan; Wang, Lizheng; Feng, Fujian; Li, Ribang

    2002-01-30

    For study the lead emission amount from coal combustion and its environment effect, the lead content of coal, ash and cinder of power station and coal-fired boiler, the lead content of dusts in the period of heating time and the non-heating time in Xi'an City were studied in this paper. The results show that amount of lead emission from 1 ton coal combustion, which lead content in coal was 30 g, was 20 g in atmosphere. The rate of lead emission of coal combustion was about 66%. About 10 million tons of coal was straight burning every year in Xi'an City and suburb, those coal mainly come from Permo-Carboniferous coal in Weibei coal mine, Shaanxi, their average lead content was 30 mg/kg. So the total lead emission from coal combustion to atmosphere was about 200 t annually in Xi'an City.

  12. 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.

  13. GHGs emission inventory in Slovakia

    SciTech Connect

    Mareckova, K.

    1996-12-31

    The results of Country Study project in Slovakia are presented. The gases included in the inventory are CO{sub 2}, CH{sub 4}, and N{sub 2}O. While the combustion of fossil fuels accounts for about 96 percent of total Slovak carbon dioxide emissions, CO{sub 2} also results directly from industrial processes. The most relevant industrial activities in Slovakia leading to CO{sub 2} emissions were cement, magnesit, and coke production. The total CO{sub 2} emissions estimated in 1990 were 60 018 Gg and 43 449 Gg in 1994. In the forestry and land use category the net CO{sub 2} flux is estimated to have been a removal. The main sources of methane emissions are livestock, natural gas distribution networks and landfills. Total CH{sub 4} emission in 1990 were estimated to be 387 Gg respectively 315 Gg in 1994. Compared to the other GHGs the emissions of N{sub 2}O are not fully understood. The main sources are expected to be agriculture soils and waste water treatment. The 21 Gg (13.5 Gg in 1994) estimated emission is still very preliminary. To evaluate the share of different GHGs and sectors, the aggregated emissions were estimated. In the year 1990 CO{sub 2} emissions amount to 79%, CH{sub 4} emissions amount to 12%, and N{sub 2}O emissions amount to 9% of total emissions, respectively 78%, 14% and 8% in 1994.

  14. 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

  15. Isoprene emission inventory for the BOREAS southern study area.

    PubMed

    Westberg, Hal; Lamb, Brian; Kempf, Kelly; Allwine, Gene

    2000-06-01

    An isoprene emission inventory for a section of boreal forest in central Saskatchewan was developed based on measured emission rates from the two dominant isoprene-emitting species, black spruce (Picea mariana (Mill.) BSP) and aspen (Populus tremuloides Michx.). The micrometeorological gradient technique was used to determine isoprene emission factors for establishing the inventory. Isoprene fluxes were measured during each of the three BOREAS intensive field campaigns (IFCs) during the 1994 growing season. Measured isoprene fluxes varied from 0.04 to 3.3 mg C m(-2) h(-1) over the black spruce canopy, and from 0.05 to 7.3 mg C m(-2) h(-1) above the aspen forest. Midsummer standard isoprene emission fluxes were 1.2 mg C m(-2) h(-1) and 2.3 mg C m(-2) h(-1) (at 20 degrees C and photosynthetically active radiation (PAR) of 1000 &mgr;mol m(-2) s(-1)) for black spruce and aspen, respectively. With light and temperature differences accounted for, there was an apparent seasonal effect on emissions with the highest rates in the summer months. The total amount of isoprene emitted from this section of the boreal forest was estimated to be 8.6 Gg C year(-1), which is about 1% of the net ecosystem carbon exchange for the study area. Aspen was the largest contributor, accounting for approximately 70% of the total. Branch enclosure and relaxed eddy accumulation measurements made at the black spruce site were used to define the uncertainty associated with flux measurements. Emission rates obtained by the gradient, enclosure and relaxed eddy accumulation methods showed good agreement when normalized to standard light and temperature conditions. The coefficient of variance between the three techniques was 12% for summer (IFC-2) measurements. The sensitivity of the annual isoprene emission total to the assignment of mean irradiance and temperature was also examined. If the hourly mean temperatures were increased by 1 degrees C throughout the growing season, annual carbon loss due to

  16. 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.

  17. Hotspots of gross emissions from the land use sector: patterns, uncertainties, and leading emission sources for the period 2000-2005 in the tropics

    NASA Astrophysics Data System (ADS)

    Roman-Cuesta, Rosa Maria; Rufino, Mariana C.; Herold, Martin; Butterbach-Bahl, Klaus; Rosenstock, Todd S.; Herrero, Mario; Ogle, Stephen; Li, Changsheng; Poulter, Benjamin; Verchot, Louis; Martius, Christopher; Stuiver, John; de Bruin, Sytze

    2016-07-01

    According to the latest report of the Intergovernmental Panel on Climate Change (IPCC), emissions must be cut by 41-72 % below 2010 levels by 2050 for a likely chance of containing the global mean temperature increase to 2 °C. The AFOLU sector (Agriculture, Forestry and Other Land Use) contributes roughly a quarter ( ˜ 10-12 Pg CO2e yr-1) of the net anthropogenic GHG emissions mainly from deforestation, fire, wood harvesting, and agricultural emissions including croplands, paddy rice, and livestock. In spite of the importance of this sector, it is unclear where the regions with hotspots of AFOLU emissions are and how uncertain these emissions are. Here we present a novel, spatially comparable dataset containing annual mean estimates of gross AFOLU emissions (CO2, CH4, N2O), associated uncertainties, and leading emission sources, in a spatially disaggregated manner (0.5°) for the tropics for the period 2000-2005. Our data highlight the following: (i) the existence of AFOLU emissions hotspots on all continents, with particular importance of evergreen rainforest deforestation in Central and South America, fire in dry forests in Africa, and both peatland emissions and agriculture in Asia; (ii) a predominant contribution of forests and CO2 to the total AFOLU emissions (69 %) and to their uncertainties (98 %); (iii) higher gross fluxes from forests, which coincide with higher uncertainties, making agricultural hotspots appealing for effective mitigation action; and (iv) a lower contribution of non-CO2 agricultural emissions to the total gross emissions (ca. 25 %), with livestock (15.5 %) and rice (7 %) leading the emissions. Gross AFOLU tropical emissions of 8.0 (5.5-12.2) were in the range of other databases (8.4 and 8.0 Pg CO2e yr-1 in FAOSTAT and the Emissions Database for Global Atmospheric Research (EDGAR) respectively), but we offer a spatially detailed benchmark for monitoring progress in reducing emissions from the land sector in the tropics. The location of

  18. 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.

  19. Comparison of two U.S. power-plant carbon dioxide emissions data sets.

    PubMed

    Ackerman, Katherine V; Sundquist, Eric T

    2008-08-01

    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 CO2 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.

  20. 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.

  1. 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.

  2. 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.

  3. 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.

  4. 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.

  5. 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.

  6. 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.

  7. 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.

  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. 40 CFR 98.213 - Calculating GHG emissions.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... the process emissions of CO2 using actual mass of output carbonates with Equation U-2 of this section... = Annual mass of input carbonate type k (tons). EFk = Emission factor for the carbonate type k, as specified in Table U-1 of this subpart (metric tons CO2/metric ton carbonate input). Mj = Annual mass...

  13. 40 CFR 98.353 - Calculating GHG emissions.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... anaerobic reactor and anaerobic lagoon from which biogas is not recovered, estimate annual CH4 emissions... wastewater treatment process n from which biogas is not recovered (metric tons). CH4Gn = Annual mass of CH4... some biogas is recovered, estimate the annual mass of CH4 recovered according to the requirements...

  14. 40 CFR 98.353 - Calculating GHG emissions.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... anaerobic reactor and anaerobic lagoon from which biogas is not recovered, estimate annual CH4 emissions... wastewater treatment process n from which biogas is not recovered (metric tons). CH4Gn = Annual mass of CH4... some biogas is recovered, estimate the annual mass of CH4 recovered according to the requirements...

  15. 40 CFR 98.353 - Calculating GHG emissions.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... anaerobic reactor and anaerobic lagoon from which biogas is not recovered, estimate annual CH4 emissions... wastewater treatment process n from which biogas is not recovered (metric tons). CH4Gn = Annual mass of CH4... biogas is recovered, estimate the annual mass of CH4 recovered according to the requirements...

  16. 40 CFR 98.353 - Calculating GHG emissions.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... anaerobic reactor and anaerobic lagoon from which biogas is not recovered, estimate annual CH4 emissions... wastewater treatment process n from which biogas is not recovered (metric tons). CH4Gn = Annual mass of CH4... some biogas is recovered, estimate the annual mass of CH4 recovered according to the requirements...

  17. Emission measurements of alkenes, alkanes, SO2, and NO2 from stationary sources in Southeast Texas over a 5 year period using SOF and mobile DOAS

    NASA Astrophysics Data System (ADS)

    Johansson, John K. E.; Mellqvist, Johan; Samuelsson, Jerker; Offerle, Brian; Lefer, Barry; Rappenglück, Bernhard; Flynn, James; Yarwood, Greg

    2014-02-01

    A mobile platform for flux measurements of VOCs (alkanes and alkenes), SO2, and NO2 emissions using the Solar Occultation Flux (SOF) method and mobile differential optical absorption spectroscopy (DOAS) was used in four different studies to measure industrial emissions. The studies were carried out in several large conglomerates of oil refineries and petrochemical industries in Southeast and East Texas in 2006, 2009, 2011, and 2012. The measured alkane emissions from the Houston Ship Channel (HSC) have been fairly stable between 2006 and 2011, averaging about 11,500 kg/h, while the alkene emissions have shown greater variations. The ethene and propene emissions measured from the HSC were 1511 kg/h and 878 kg/h, respectively, in 2006, while dropping to roughly 600 kg/h for both species in 2009 and 2011. The results were compared to annual inventory emissions, showing that measured VOC emissions were typically 5-15 times higher, while for SO2 and NO2 the ratio was typically 0.5-2. AP-42 emission factors were used to estimate meteorological effects on alkane emissions from tanks, showing that these emissions may have been up to 35-45% higher during the studies than the annual average. A more focused study of alkene emissions from a petrochemical complex in Longview in 2012 identified two upset episodes, and the elevation of the total emissions during the measurement period due to the upsets was estimated to be approximately 20%. Both meteorological and upset effects were small compared to the factor of 5-15, suggesting that VOC emissions are systematically and substantially underestimated in current emission inventories.

  18. Volatile compounds emission from canopy fine litterfall in a hemiboreal mixed forest at Järvselja

    NASA Astrophysics Data System (ADS)

    Portillo-Estrada, Miguel; Noe, Beate; Noe, Steffen M.

    2013-04-01

    The seasonal distribution of biogenic volatile organic compounds (BVOC) emissions from canopy fine litterfall was investigated over a period of two years. Three stands of a hemiboreal mixed forest were studied. The stands presented different dominant tree species: (1) Norway spruce, (2) Scots pine, and (3) Silver birch and Downy birch. The litterfall was monthly collected in litter traps. The BVOC emission of litter was sampled by placing the litter into a glass jar equipped with a vent tube and pumping the head space air through a VOC adsorbing tube (carbotrap). Adsorbed BVOCs were analyzed in a GC-MS. Fifteen compounds were quantified. Seasonal differences in the total emission of BVOCs were found, defined by a maximum in summer and a minimum in autumn and winter. During summer months, litter emissions were dominated by limonene, α-pinene, camphene and 3-carene in the three litter types, accounting for 70-75 % of total BVOC emitted in June. 3-Carene, α-pinene and β-pinene were the main compounds emitted during winter time, accounting for 50-60 % of total BVOC emitted in January. Stand to stand differences were assessed. The spruce and birch dominated stands showed more similarities in their BVOC emission pattern if compared to the pine dominated stand. Together with the litterfall data, an estimation of the annual total BVOC emitted by the soil litter layer is presented for each stand type.

  19. 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

  20. The FAOSTAT database of greenhouse gas emissions from agriculture

    NASA Astrophysics Data System (ADS)

    Tubiello, Francesco N.; Salvatore, Mirella; Rossi, Simone; Ferrara, Alessandro; Fitton, Nuala; Smith, Pete

    2013-03-01

    Greenhouse gas (GHG) emissions from agriculture, including crop and livestock production, forestry and associated land use changes, are responsible for a significant fraction of anthropogenic emissions, up to 30% according to the Intergovernmental Panel on Climate Change (IPCC). Yet while emissions from fossil fuels are updated yearly and by multiple sources—including national-level statistics from the International Energy Agency (IEA)—no comparable efforts for reporting global statistics for agriculture, forestry and other land use (AFOLU) emissions exist: the latest complete assessment was the 2007 IPCC report, based on 2005 emission data. This gap is critical for several reasons. First, potentially large climate funding could be linked in coming decades to more precise estimates of emissions and mitigation potentials. For many developing countries, and especially the least developed ones, this requires improved assessments of AFOLU emissions. Second, growth in global emissions from fossil fuels has outpaced that from AFOLU during every decade of the period 1961-2010, so the relative contribution of the latter to total climate forcing has diminished over time, with a need for regular updates. We present results from a new GHG database developed at FAO, providing a complete and coherent time series of emission statistics over a reference period 1961-2010, at country level, based on FAOSTAT activity data and IPCC Tier 1 methodology. We discuss results at global and regional level, focusing on trends in the agriculture sector and net deforestation. Our results complement those available from the IPCC, extending trend analysis to a longer historical period and, critically, beyond 2005 to more recent years. In particular, from 2000 to 2010, we find that agricultural emissions increased by 1.1% annually, reaching 4.6 Gt CO2 yr-1 in 2010 (up to 5.4-5.8 Gt CO2 yr-1 with emissions from biomass burning and organic soils included). Over the same decade 2000-2010, the

  1. 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.

  2. [Estimation of carbonaceous gases emission from forest fires in Xiao Xing'an Mountains of Northeast China in 1953-2011].

    PubMed

    Hu, Hai-Qing; Luo, Bi-Zhen; Wei, Shu-Jing; Sun, Long; Wei, Shu-Wei; Wen, Zheng-Min

    2013-11-01

    Based on the forest resources investigation data and the forest fire inventory in 1953-2011, in combining with our field research in burned areas and our laboratory experiments, this paper estimated the carbonaceous gases carbon dioxide (CO2), carbon monoxide (CO), methane (CH4), and nonmethane hydrocarbons (NMHC) emission from the forest fires in Xiao Xing' an Mountains of Heilongjiang Province, Northeast China in 1953-2011. The total carbon emission from the forest fires in the Xiao Xing'an Mountains in 1953-2011 was 1.12 x 10(7) t, and the annual emission was averagely 1.90 x10(5) t, accounting for 1.7% of the annual average total carbon emission from the forest fires in China. The emission of CO2, CO, CH4, and NMHC was 3.39 x 10(7), 1.94 x 10(5), 1.09 x 10(5), and 7.46 x 10(4) t, respectively, and the corresponding annual average emission was 5.74 x 10(5), 3.29 x 10(4), 1.85 x 10(3), and 1.27 x 10(3) t, accounting for 1.4%, 1.2%, 1.7%, and 1.1% of the annual carbonaceous gases emitted from the forest fires in China, respectively. The combustion efficiency and the carbon emission per unit burned area of different forest types decreased in order of coniferous forest > broad-leaved forest > coniferous broadleaved mixed forest. Some rational forest fire management measures were put forward.

  3. Temporalization of peak electric generation particulate matter emissions during high energy demand days.

    PubMed

    Farkas, Caroline M; Moeller, Michael D; Felder, Frank A; Baker, Kirk R; Rodgers, Mark; Carlton, Annmarie G

    2015-04-01

    Underprediction of peak ambient pollution by air quality models hinders development of effective strategies to protect health and welfare. The U.S. Environmental Protection Agency's community multiscale air quality (CMAQ) model routinely underpredicts peak ozone and fine particulate matter (PM2.5) concentrations. Temporal misallocation of electricity sector emissions contributes to this modeling deficiency. Hourly emissions are created for CMAQ by use of temporal profiles applied to annual emission totals unless a source is matched to a continuous emissions monitor (CEM) in the National Emissions Inventory (NEI). More than 53% of CEMs in the Pennsylvania-New Jersey-Maryland (PJM) electricity market and 45% nationally are unmatched in the 2008 NEI. For July 2006, a United States heat wave with high electricity demand, peak electric sector emissions, and elevated ambient PM2.5 mass, we match hourly emissions for 267 CEM/NEI pairs in PJM (approximately 49% and 12% of unmatched CEMs in PJM and nationwide) using state permits, electricity dispatch modeling and CEMs. Hourly emissions for individual facilities can differ up to 154% during the simulation when measurement data is used rather than default temporalization values. Maximum CMAQ PM2.5 mass, sulfate, and elemental carbon predictions increase up to 83%, 103%, and 310%, at the surface and 51%, 75%, and 38% aloft (800 mb), respectively. PMID:25705922

  4. Emission estimates of particulate matter and heavy metals from mobile sources in Delhi (India).

    PubMed

    Kumari, Ragini; Attri, Arun K; Panis, Luc Int; Gurjar, B R

    2013-04-01

    An attempt has been made to make a comprehensive emission inventory of particulate matter (PM) of various size fractions and also of heavy metals (HMs) emitted from mobile sources (both exhaust and non-exhaust) from the road transport of Delhi, India (1991-2006). COPERT-III and 4 models were mainly used toestimate these emissions. Results show that the annual exhaust emission of PM of size upto 2.5 micrometer (PM2.5) has increased from 3Gg to 4.5Gg during 1991-2006 irrespective of'improvement in vehicle-technology and fuel use. PM emission from exhaust and non-exhaust sources in general has increased. Heavy commercial vehicles-need attention to control particulate emission as it emerged as a predominant source of PM emissions. Among non-exhaust emissions of total suspended particulate matter (TSP), road-surface wear (~49%) has the prime contribution. As a result of-introduction of unleaded gasoline Pb has significantly reduced (~8 fold) whereas share of Cu and Zn are still considerable. Among non-exhaust sources, Pb release was the most significant one from tyre-wear whereas from break-wear, Cu release was found to be the most significant followed by Pb and Cr + Zn. Because of public health concerns further policies need to be developed to reduce emissions of PM and HMs from the road transport of megacity Delhi. PMID:25464689

  5. Emission estimates of particulate matter and heavy metals from mobile sources in Delhi (India).

    PubMed

    Kumari, Ragini; Attri, Arun K; Panis, Luc Int; Gurjar, B R

    2013-04-01

    An attempt has been made to make a comprehensive emission inventory of particulate matter (PM) of various size fractions and also of heavy metals (HMs) emitted from mobile sources (both exhaust and non-exhaust) from the road transport of Delhi, India (1991-2006). COPERT-III and 4 models were mainly used toestimate these emissions. Results show that the annual exhaust emission of PM of size upto 2.5 micrometer (PM2.5) has increased from 3Gg to 4.5Gg during 1991-2006 irrespective of'improvement in vehicle-technology and fuel use. PM emission from exhaust and non-exhaust sources in general has increased. Heavy commercial vehicles-need attention to control particulate emission as it emerged as a predominant source of PM emissions. Among non-exhaust emissions of total suspended particulate matter (TSP), road-surface wear (~49%) has the prime contribution. As a result of-introduction of unleaded gasoline Pb has significantly reduced (~8 fold) whereas share of Cu and Zn are still considerable. Among non-exhaust sources, Pb release was the most significant one from tyre-wear whereas from break-wear, Cu release was found to be the most significant followed by Pb and Cr + Zn. Because of public health concerns further policies need to be developed to reduce emissions of PM and HMs from the road transport of megacity Delhi. PMID:25508320

  6. A probabilistic approach to emissions from transportation sector in the coming decades

    NASA Astrophysics Data System (ADS)

    Yan, F.; Winijkul, E.; Bond, T. C.; Streets, D. G.

    2010-12-01

    how these uncertainties will affect total emissions if any input parameter that has inherent the uncertainties is substituted by a range of values-probability distribution and varies at the same time; the 95% confidence interval of global emission annual growth rate is -1.9% to +0.2% per year.

  7. Monthly, global emissions of carbon dioxide from fossil fuel consumption

    SciTech Connect

    Andres, Robert Joseph; Gregg, JS; Losey, London M; Marland, Gregg; Boden, Thomas A

    2011-01-01

    This paper examines available data, develops a strategy and presents a monthly, global time series of fossil-fuel carbon dioxide emissions for the years 1950 2006. This monthly time series was constructed from detailed study of monthly data from the 21 countries that account for approximately 80% of global total emissions. These data were then used in a Monte Carlo approach to proxy for all remaining countries. The proportional-proxy methodology estimates by fuel group the fraction of annual emissions emitted in each country and month. Emissions from solid, liquid and gas fuels are explicitly modelled by the proportional-proxy method. The primary conclusion from this study is the global monthly time series is statistically significantly different from a uniform distribution throughout the year. Uncertainty analysis of the data presented show that the proportional-proxy method used faithfully reproduces monthly patterns in the data and the global monthly pattern of emissions is relatively insensitive to the exact proxy assignments used. The data and results presented here should lead to a better understanding of global and regional carbon cycles, especially when the mass data are combined with the stable carbon isotope data in atmospheric transport models.

  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. Inventory of methane emissions from U.S. cattle

    NASA Astrophysics Data System (ADS)

    Westberg, H.; Lamb, B.; Johnson, K. A.; Huyler, M.

    2001-01-01

    Many countries, including the United States, are in the process of inventorying greenhouse gas emissions as a prerequisite for designing control strategies. We have developed a measurement-based inventory of methane emissions from cattle in the United States. Methane emission factors were established for the major livestock groups using an internal tracer method. The groups studied included cows, replacement heifers, slaughter cattle, calves, and bulls in the beef sector and cows plus replacement heifers in the dairy industry. Since methane emission is dependent on the quality and quantity of feed, diets were chosen that are representative of the feed regimes utilized by producers in the United States. Regional cattle populations, obtained from U.S. Department of Agriculture statistics, were combined with the methane emission factors to yield regional emission estimates. The methane totals from the five regions were then summed to give a U.S. inventory of cattle emissions for 1990, 1992, 1994, 1996, and 1998. Annual releases ranged from 6.50 Tg in 1990 to a high of 6.98 Tg in 1996. On a regional scale the North Central region of the United States had the largest methane emissions from livestock followed by the South Central and the West. The beef cow group released the most methane (˜2.5 Tg yr-1) followed by slaughter cattle (˜1.7 Tg yr-1) and dairy cows at about 1.5 Tg yr-1. Methane released by cattle in the United States contributes about 11% of the global cattle source.

  10. 40 CFR 61.24 - Annual reporting requirements.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 9 2012-07-01 2012-07-01 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...

  11. 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...

  12. 40 CFR 61.254 - 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. 61.254 Section 61.254 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS National Emission Standards for...

  13. 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...

  14. 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...

  15. 40 CFR 61.254 - Annual reporting requirements.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 9 2012-07-01 2012-07-01 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...

  16. 40 CFR 61.254 - 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. 61.254 Section 61.254 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS National Emission Standards for...

  17. 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...

  18. 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...

  19. 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...

  20. Emission Database for Global Atmospheric Research (EDGAR).

    ERIC Educational Resources Information Center

    Olivier, J. G. J.; And Others

    1994-01-01

    Presents the objective and methodology chosen for the construction of a global emissions source database called EDGAR and the structural design of the database system. The database estimates on a regional and grid basis, 1990 annual emissions of greenhouse gases, and of ozone depleting compounds from all known sources. (LZ)

  1. Methane and carbon dioxide emissions from 40 lakes along a north–south latitudinal transect in Alaska

    DOE PAGESBeta

    Sepulveda-Jauregui, A.; Walter Anthony, K. M.; Martinez-Cruz, K.; Greene, S.; Thalasso, F.

    2014-09-12

    Uncertainties in the magnitude and seasonality of various gas emission modes, particularly among different lake types, limit our ability to estimate methane (CH4) and carbon dioxide (CO2) emissions from northern lakes. Here we assessed the relationship between CH4 and CO2 emission modes in 40 lakes along a latitudinal transect in Alaska to physicochemical limnology and geographic characteristics, including permafrost soil type surrounding lakes. Emission modes included Direct Ebullition, Diffusion, Storage flux, and a newly identified Ice-Bubble Storage (IBS) flux. We found that all lakes were net sources of atmospheric CH4 and CO2, but the climate warming impact of lake CH4more » emissions was two times higher than that of CO2. Ebullition and Diffusion were the dominant modes of CH4 and CO2 emissions respectively. IBS, ~ 10% of total annual CH4 emissions, is the release to the atmosphere of seasonally ice-trapped bubbles when lake ice confining bubbles begins to melt in spring. IBS, which has not been explicitly accounted for in regional studies, increased the estimate of springtime emissions from our study lakes by 320%. Geographically, CH4 emissions from stratified, dystrophic interior Alaska thermokarst (thaw) lakes formed in icy, organic-rich yedoma permafrost soils were 6-fold higher than from non-yedoma lakes throughout the rest of Alaska. Total CH4 emission was correlated with concentrations of phosphate and total nitrogen in lake water, Secchi depth and lake area, with yedoma lakes having higher nutrient concentrations, shallower Secchi depth, and smaller lake areas. Our findings suggest that permafrost type plays important roles in determining CH4 emissions from lakes by both supplying organic matter to methanogenesis directly from thawing permafrost and by enhancing nutrient availability to primary production, which can also fuel decomposition and methanogenesis.« less

  2. 40 CFR 60.1730 - How do I make sure my continuous emission monitoring systems are operating correctly?

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... annual evaluations of your continuous emission monitoring systems that measure oxygen (or carbon dioxide... to 60 minutes) using your oxygen (or carbon dioxide) continuous emission monitoring system, your sulfur dioxide, nitrogen oxides, or carbon monoxide continuous emission monitoring systems,...

  3. Measurements of methane emissions at natural gas production sites in the United States

    PubMed Central

    Allen, David T.; Torres, Vincent M.; Thomas, James; Sullivan, David W.; Harrison, Matthew; Hendler, Al; Herndon, Scott C.; Kolb, Charles E.; Fraser, Matthew P.; Hill, A. Daniel; Lamb, Brian K.; Miskimins, Jennifer; Sawyer, Robert F.; Seinfeld, John H.

    2013-01-01

    Engineering estimates of methane emissions from natural gas production have led to varied projections of national emissions. This work reports direct measurements of methane emissions at 190 onshore natural gas sites in the United States (150 production sites, 27 well completion flowbacks, 9 well unloadings, and 4 workovers). For well completion flowbacks, which clear fractured wells of liquid to allow gas production, methane emissions ranged from 0.01 Mg to 17 Mg (mean = 1.7 Mg; 95% confidence bounds of 0.67–3.3 Mg), compared with an average of 81 Mg per event in the 2011 EPA national emission inventory from April 2013. Emission factors for pneumatic pumps and controllers as well as equipment leaks were both comparable to and higher than estimates in the national inventory. Overall, if emission factors from this work for completion flowbacks, equipment leaks, and pneumatic pumps and controllers are assumed to be representative of national populations and are used to estimate national emissions, total annual emissions from these source categories are calculated to be 957 Gg of methane (with sampling and measurement uncertainties estimated at ±200 Gg). The estimate for comparable source categories in the EPA national inventory is ∼1,200 Gg. Additional measurements of unloadings and workovers are needed to produce national emission estimates for these source categories. The 957 Gg in emissions for completion flowbacks, pneumatics, and equipment leaks, coupled with EPA national inventory estimates for other categories, leads to an estimated 2,300 Gg of methane emissions from natural gas production (0.42% of gross gas production). PMID:24043804

  4. Estimating nitrogen oxides emissions at city scale in China with a nightlight remote sensing model.

    PubMed

    Jiang, Jianhui; Zhang, Jianying; Zhang, Yangwei; Zhang, Chunlong; Tian, Guangming

    2016-02-15

    Increasing nitrogen oxides (NOx) emissions over the fast developing regions have been of great concern due to their critical associations with the aggravated haze and climate change. However, little geographically specific data exists for estimating spatio-temporal trends of NOx emissions. In order to quantify the spatial and temporal variations of NOx emissions, a spatially explicit approach based on the continuous satellite observations of artificial nighttime stable lights (NSLs) from the Defense Meteorological Satellite Program/Operational Linescan System (DMSP/OLS) was developed to estimate NOx emissions from the largest emission source of fossil fuel combustion. The NSL based model was established with three types of data including satellite data of nighttime stable lights, geographical data of administrative boundaries, and provincial energy consumptions in China, where a significant growth of NOx emission has experienced during three policy stages corresponding to the 9th-11th)Five-Year Plan (FYP, 1995-2010). The estimated national NOx emissions increased by 8.2% per year during the study period, and the total annual NOx emissions in China estimated by the NSL-based model were approximately 4.1%-13.8% higher than the previous estimates. The spatio-temporal variations of NOx emissions at city scale were then evaluated by the Moran's I indices. The global Moran's I indices for measuring spatial agglomerations of China's NOx emission increased by 50.7% during 1995-2010. Although the inland cities have shown larger contribution to the emission growth than the more developed coastal cities since 2005, the High-High clusters of NOx emission located in Beijing-Tianjin-Hebei regions, the Yangtze River Delta, and the Pearl River Delta should still be the major focus of NOx mitigation. Our results indicate that the readily available DMSP/OLS nighttime stable lights based model could be an easily accessible and effective tool for achieving strategic decision making

  5. Quantification of methane emissions from 15 Danish landfills using the mobile tracer dispersion method

    SciTech Connect

    Mønster, Jacob; Samuelsson, Jerker; Scheutz, Charlotte

    2015-01-15

    Highlights: • Quantification of whole landfill site methane emission at 15 landfills. • Multiple on-site source identification and quantification. • Quantified methane emission from shredder waste and composting. • Large difference between measured and reported methane emissions. - Abstract: Whole-site methane emissions from 15 Danish landfills were assessed using a mobile tracer dispersion method with either Fourier transform infrared spectroscopy (FTIR), using nitrous oxide as a tracer gas, or cavity ring-down spectrometry (CRDS), using acetylene as a tracer gas. The landfills were chosen to represent the different stages of the lifetime of a landfill, including open, active, and closed covered landfills, as well as those with and without gas extraction for utilisation or flaring. Measurements also included landfills with biocover for oxidizing any fugitive methane. Methane emission rates ranged from 2.6 to 60.8 kg h{sup −1}, corresponding to 0.7–13.2 g m{sup −2} d{sup −1}, with the largest emission rates per area coming from landfills with malfunctioning gas extraction systems installed, and the smallest emission rates from landfills closed decades ago and landfills with an engineered biocover installed. Landfills with gas collection and recovery systems had a recovery efficiency of 41–81%. Landfills where shredder waste was deposited showed significant methane emissions, with the largest emission from newly deposited shredder waste. The average methane emission from the landfills was 154 tons y{sup −1}. This average was obtained from a few measurement campaigns conducted at each of the 15 landfills and extrapolating to annual emissions requires more measurements. Assuming that these landfills are representative of the average Danish landfill, the total emission from Danish landfills were calculated at 20,600 tons y{sup −1}, which is significantly lower than the 33,300 tons y{sup −1} estimated for the national greenhouse gas inventory for

  6. Measurements of methane emissions at natural gas production sites in the United States.

    PubMed

    Allen, David T; Torres, Vincent M; Thomas, James; Sullivan, David W; Harrison, Matthew; Hendler, Al; Herndon, Scott C; Kolb, Charles E; Fraser, Matthew P; Hill, A Daniel; Lamb, Brian K; Miskimins, Jennifer; Sawyer, Robert F; Seinfeld, John H

    2013-10-29

    Engineering estimates of methane emissions from natural gas production have led to varied projections of national emissions. This work reports direct measurements of methane emissions at 190 onshore natural gas sites in the United States (150 production sites, 27 well completion flowbacks, 9 well unloadings, and 4 workovers). For well completion flowbacks, which clear fractured wells of liquid to allow gas production, methane emissions ranged from 0.01 Mg to 17 Mg (mean = 1.7 Mg; 95% confidence bounds of 0.67-3.3 Mg), compared with an average of 81 Mg per event in the 2011 EPA national emission inventory from April 2013. Emission factors for pneumatic pumps and controllers as well as equipment leaks were both comparable to and higher than estimates in the national inventory. Overall, if emission factors from this work for completion flowbacks, equipment leaks, and pneumatic pumps and controllers are assumed to be representative of national populations and are used to estimate national emissions, total annual emissions from these source categories are calculated to be 957 Gg of methane (with sampling and measurement uncertainties estimated at ± 200 Gg). The estimate for comparable source categories in the EPA national inventory is ~1,200 Gg. Additional measurements of unloadings and workovers are needed to produce national emission estimates for these source categories. The 957 Gg in emissions for completion flowbacks, pneumatics, and equipment leaks, coupled with EPA national inventory estimates for other categories, leads to an estimated 2,300 Gg of methane emissions from natural gas production (0.42% of gross gas production).

  7. Ammonia emissions from naturally ventilated dairy cattle buildings and outdoor concrete yards in Portugal

    NASA Astrophysics Data System (ADS)

    Pereira, José; Misselbrook, Tom H.; Chadwick, David R.; Coutinho, João; Trindade, Henrique

    2010-09-01

    There is a lack of information on ammonia (NH 3) emissions from cattle housing systems in Mediterranean countries, with most published data deriving from NW Europe. An investigation was carried out in NW Portugal to quantify NH 3 emissions for the main types of dairy cattle buildings in Portugal, i.e. naturally ventilated buildings and outdoor concrete yards, and to derive robust emission factors (EFs) for these conditions and compare with EFs used elsewhere in Europe. Measurements were made throughout a 12-month period using the passive flux sampling method in the livestock buildings and the equilibrium concentration technique in outdoor yards. The mean NH 3 emission factor for the whole housing system (buildings + outdoor yards) was 43.7 g NH 3-N LU -1 day -1 and for outdoor concrete yards used by dairy cattle was 26.6 g NH 3-N LU -1 day -1. Expressing NH 3 emission in terms of the quantity of liquid milk produced gave similar values across the three dairy farms studied (with a mean of 2.3 kg N ton-milk -1 produced) and may have advantages when comparing different farming systems. In dairy houses with outdoor yards, NH 3 emissions from the yard area contributed to 69-92% of total emissions from this housing system. Emissions were particularly important during spring and summer seasons from outdoor yards with NH 3 emitted in this period accounting for about 72% of annual emissions from outdoor yards. Mean NH 3 emission factors derived for this freestall housing system and outdoor concrete yards used by dairy cattle in Portugal were higher than those measured in northern Europe. In addition, values of animal N excretion estimated in this study were greater than official National standard values. If these emissions are typical for Portuguese dairy systems, then the current National inventory underestimates emissions from this source in NW of Portugal, because of the use of lower standard values of N excretion by dairy cattle.

  8. Estimating nitrogen oxides emissions at city scale in China with a nightlight remote sensing model.

    PubMed

    Jiang, Jianhui; Zhang, Jianying; Zhang, Yangwei; Zhang, Chunlong; Tian, Guangming

    2016-02-15

    Increasing nitrogen oxides (NOx) emissions over the fast developing regions have been of great concern due to their critical associations with the aggravated haze and climate change. However, little geographically specific data exists for estimating spatio-temporal trends of NOx emissions. In order to quantify the spatial and temporal variations of NOx emissions, a spatially explicit approach based on the continuous satellite observations of artificial nighttime stable lights (NSLs) from the Defense Meteorological Satellite Program/Operational Linescan System (DMSP/OLS) was developed to estimate NOx emissions from the largest emission source of fossil fuel combustion. The NSL based model was established with three types of data including satellite data of nighttime stable lights, geographical data of administrative boundaries, and provincial energy consumptions in China, where a significant growth of NOx emission has experienced during three policy stages corresponding to the 9th-11th)Five-Year Plan (FYP, 1995-2010). The estimated national NOx emissions increased by 8.2% per year during the study period, and the total annual NOx emissions in China estimated by the NSL-based model were approximately 4.1%-13.8% higher than the previous estimates. The spatio-temporal variations of NOx emissions at city scale were then evaluated by the Moran's I indices. The global Moran's I indices for measuring spatial agglomerations of China's NOx emission increased by 50.7% during 1995-2010. Although the inland cities have shown larger contribution to the emission growth than the more developed coastal cities since 2005, the High-High clusters of NOx emission located in Beijing-Tianjin-Hebei regions, the Yangtze River Delta, and the Pearl River Delta should still be the major focus of NOx mitigation. Our results indicate that the readily available DMSP/OLS nighttime stable lights based model could be an easily accessible and effective tool for achieving strategic decision making

  9. Annual Fund. Estate Planning.

    ERIC Educational Resources Information Center

    Stuhr, Robert L.; Jarc, Jerry A.

    The first of a series, this publication consists of two symposium presentations. The first paper, "Annual Fund: Cornerstone of Development," by Robert L. Stuhr, defines the annual fund concept in the context of institutional development and provides five requisites for a successful annual fund: it must (1) be part of an ongoing development…

  10. Air Permit Compliance for Hanford Waste Retrieval Operations Involving Multi-Unit Emissions

    SciTech Connect

    Faulk, D.E.; Simmons, F.M.

    2008-07-01

    Since 1970, approximately 38,000 suspect-transuranic and transuranic waste containers have been placed in retrievable storage on the Hanford Site in the 200 Areas burial grounds. Hanford's Waste Retrieval Project is retrieving these buried containers and processing them for safe storage and disposition. Container retrieval activities require an air emissions permit to account for potential emissions of radionuclides. The air permit covers the excavation activities as well as activities associated with assaying containers and installing filters in the retrieved transuranic containers lacking proper venting devices. Fluor Hanford, Inc. is required to track radioactive emissions resulting from the retrieval activities. Air, soil, and debris media contribute to the emissions and enabling assumptions allow for calculation of emissions. Each of these activities is limited to an allowed annual emission (per calendar year) and contributes to the overall total emissions allowed for waste retrieval operations. Tracking these emissions is required to ensure a permit exceedance does not occur. A tracking tool was developed to calculate potential emissions in real time sense. Logic evaluations are established within the tracking system to compare real time data against license limits to ensure values are not exceeded for either an individual activity or the total limit. Data input are based on field survey and workplace air monitoring activities. This tracking tool is used monthly and quarterly to verify compliance to the license limits. Use of this tool has allowed Fluor Hanford, Inc. to successfully retrieve a significant number of containers in a safe manner without any exceedance of emission limits. (authors)

  11. Emissivity of microstructured silicon.

    PubMed

    Maloney, Patrick G; Smith, Peter; King, Vernon; Billman, Curtis; Winkler, Mark; Mazur, Eric

    2010-03-01

    Infrared transmittance and hemispherical-directional reflectance data from 2.5 to 25 microm on microstructured silicon surfaces have been measured, and spectral emissivity has been calculated for this wavelength range. Hemispherical-total emissivity is calculated for the samples and found to be 0.84 before a measurement-induced annealing and 0.65 after the measurement for the sulfur-doped sample. Secondary samples lack a measurement-induced anneal, and reasons for this discrepancy are presented. Emissivity numbers are plotted and compared with a silicon substrate, and Aeroglaze Z306 black paint. Use of microstructured silicon as a blackbody or microbolometer surface is modeled and presented, respectively.

  12. What is the impact of Harmattan surges on desert dust emission in North Africa?

    NASA Astrophysics Data System (ADS)

    Fiedler, Stephanie; Kaplan, Michael L.; Knippertz, Peter

    2015-04-01

    Desert dust aerosols have important implications in the Earth system, but their emission amount has a large model uncertainty. Improving the most important meteorological processes for dust-emitting winds helps to reduce this uncertainty. However, the dominant meteorological mechanisms for the large dust emission during spring remain unclear. This time of year is characterized by mobile, long-lived cyclones and Harmattan surges which are capable to uplift dust aerosol for long-range atmospheric transport. Emission near to the centre of mobile, long-lived cyclones are associated with a small mass of dust emission over the northern Sahara in spring, despite their most frequent occurrence in this season. Harmattan surges are proposed to be more efficient in emitting dust aerosol in spring. These events manifest themselves as a postfrontal strengthening of near-surface winds with a continental impact on dust emission. The present study shows the first long-term climatology of dust emission associated with Harmattan surges over North Africa. Using a newly-developed automated identification, Harmattan surges are statistically analysed in 32 years of ERA-Interim re-analysis from the European Centre for Medium-Range Weather Forecasts. The results show 34 events per year in the annual mean. Spring is herein the most active season with the largest mean number and duration of Harmattan surges, in contrast to summer with virtually no activity. The offline dust emission model by Tegen et al (2002) is used to calculate emissions with ERA-Interim data. Combining these results with the Harmattan surges allows a first quantitative estimate of the associated emission mass. The results highlight that a fraction of 32 % of the total emission is associated with these events, annually and spatially averaged across North Africa. This amount exceeds the annual mean contribution of nocturnal low-level jets to dust emission, which is known as one of the most important drivers for North

  13. Trends and Projected Estimates of GHG Emissions from Indian Livestock in Comparisons with GHG Emissions from World and Developing Countries.

    PubMed

    Patra, Amlan Kumar

    2014-04-01

    This study presents trends and projected estimates of methane and nitrous oxide emissions from livestock of India vis-à-vis world and developing countries over the period 1961 to 2010 estimated based on IPCC guidelines. World enteric methane emission (EME) increased by 54.3% (61.5 to 94.9 ×10(9) kg annually) from the year 1961 to 2010, and the highest annual growth rate (AGR) was noted for goat (2.0%), followed by buffalo (1.57%) and swine (1.53%). Global EME is projected to increase to 120×10(9) kg by 2050. The percentage increase in EME by Indian livestock was greater than world livestock (70.6% vs 54.3%) between the years 1961 to 2010, and AGR was highest for goat (1.91%), followed by buffalo (1.55%), swine (1.28%), sheep (1.25%) and cattle (0.70%). In India, total EME was projected to grow by 18.8×10(9) kg in 2050. Global methane emission from manure (MEM) increased from 6.81 ×10(9) kg in 1961 to 11.4×10(9) kg in 2010 (an increase of 67.6%), and is projected to grow to 15×10(9) kg by 2050. In India, the annual MEM increased from 0.52×10(9) kg to 1.1×10(9) kg (with an AGR of 1.57%) in this period, which could increase to 1.54×10(9) kg in 2050. Nitrous oxide emission from manure in India could be 21.4×10(6) kg in 2050 from 15.3×10(6) kg in 2010. The AGR of global GHG emissions changed a small extent (only 0.11%) from developed countries, but increased drastically (1.23%) for developing countries between the periods of 1961 to 2010. Major contributions to world GHG came from cattle (79.3%), swine (9.57%) and sheep (7.40%), and for developing countries from cattle (68.3%), buffalo (13.7%) and goat (5.4%). The increase of GHG emissions by Indian livestock was less (74% vs 82% over the period of 1961 to 2010) than the developing countries. With this trend, world GHG emissions could reach 3,520×10(9) kg CO2-eq by 2050 due to animal population growth driven by increased demands for meat and dairy products in the world.

  14. 2009 LANL radionuclide air emissions report

    SciTech Connect

    Fuehne, David P.

    2010-06-01

    The emissions of radionuclides from Department of Energy Facilities such as Los Alamos National Laboratory (LANL) are regulated by the Amendments to the Clean Air Act of 1990, National Emissions Standards for Hazardous Air Pollutants (40 CFR 61 Subpart H). These regulations established an annual dose limit of 10 mrem to the maximally exposed member of the public attributable to emissions of radionuclides. This document describes the emissions of radionuclides from LANL and the dose calculations resulting from these emissions for calendar year 2009. This report meets the reporting requirements established in the regulations.

  15. 2008 LANL radionuclide air emissions report

    SciTech Connect

    Fuehne, David P.

    2009-06-01

    The emissions of radionuclides from Department of Energy Facilities such as Los Alamos National Laboratory (LANL) are regulated by the Amendments to the Clean Air Act of 1990, National Emissions Standards for Hazardous Air Pollutants (40 CFR 61 Subpart H). These regulations established an annual dose limit of 10 mrem to the maximally exposed member of the public attributable to emissions of radionuclides. This document describes the emissions of radionuclides from LANL and the dose calculations resulting from these emissions for calendar year 2008. This report meets the reporting requirements established in the regulations.

  16. 2010 LANL radionuclide air emissions report /

    SciTech Connect

    Fuehne, David P.

    2011-06-01

    The emissions of radionuclides from Department of Energy Facilities such as Los Alamos National Laboratory (LANL) are regulated by the Amendments to the Clean Air Act of 1990, National Emissions Standards for Hazardous Air Pollutants (40 CFR 61 Subpart H). These regulations established an annual dose limit of 10 mrem to the maximally exposed member of the public attributable to emissions of radionuclides. This document describes the emissions of radionuclides from LANL and the dose calculations resulting from these emissions for calendar year 2010. This report meets the reporting requirements established in the regulations.

  17. Ammonia emissions from outdoor concrete yards used by livestock—quantification and mitigation

    NASA Astrophysics Data System (ADS)

    Misselbrook, T. H.; Webb, J.; Gilhespy, S. L.

    Outdoor concrete yards are commonly found on UK livestock farms, and, to a lesser extent, elsewhere in Europe, and represent a potentially significant source of ammonia (NH 3) emissions to the atmosphere. This study provided further measurements from a larger sample than previously made, to improve the robustness of the estimate of total NH 3 emission for inclusion in the UK NH 3 emission inventory. In addition, an assessment was made of a number of potential mitigation strategies. Measurements were made using the equilibrium concentration technique, employing small dynamic chambers and passive diffusion samplers, from 20 yards used by livestock on commercial farms. Mean emission rates (±standard error) were 0.31±0.07, 0.23±0.12, 0.19±0.05 and 0.18±0.09 g NH 3-N m -2 h -1 (0.70±0.21, 0.53±0.34, 0.76±0.22 and 0.18±0.14 g NH 3-N animal -1 h -1) for dairy cow-collecting yards, dairy cow-feeding yards, beef-feeding yards and sheep-feeding/handling areas, respectively, with mean respective livestock densities of 0.3, 0.5, 0.2 and 1.1 animals per m 2. There was a significant effect of season, with lower emission rates in the winter. There was a significant, albeit poor, positive linear relationship between emission rate and ambient air temperature ( r2=0.22) and between emission rate and total ammoniacal N content on the yard surface ( r2=0.14), but not with ambient wind speed. Pooling data from the present study with that from previous studies gave mean emission factors of 0.47±0.09, 0.98±0.39 and 0.13±0.09 g NH 3-N animal -1 h -1 for yards used by dairy cattle, beef cattle and sheep, respectively. Inclusion of these values, together with survey data on yard use, gave a total annual UK emission of approximately 25 kt NH 3 (95% confidence interval of 12-40 kt NH 3), representing almost 10% of total NH 3 emission from UK agriculture. In controlled studies, pressure washing and the use of a urease inhibitor in addition to yard scraping were found to be

  18. N2O emissions from streams in the Neuse river watershed, North Carolina.

    PubMed

    Stow, Craig A; Walker, John T; Cardoch, Lynette; Spence, Porche; Geron, Chris

    2005-09-15

    We present N2O emission data from 11 sites in the Neuse River watershed. Emissions were measured using a static surface enclosure technique deployed on eight sites on the main river channel and three tributary sites. Ancillary data collected included dissolved oxygen, nitrate, total nitrogen, ammonium, dissolved organic carbon, total phosphorus, and temperature. Analysis using standard linear models, and classification and regression trees (CART), indicated nitrate to be the primary driving variable associated with N2O emission, although dissolved organic carbon concentration and water temperature were positively related with N2O emission as well. Relationships between nitrate concentration and N2O emission were consistent with those found in previous studies, although the data presented here represent the lower end of the range for both variables among published studies. Using our measured N2O emission rates along with literature values for the ratio of nitrogen gas to N2O produced during denitrification, we estimate N loss via denitrification in the Neuse River is approximately 17% of the annual N load delivered to the estuary.

  19. CO2 annual and semiannual cycles from multiple satellite retrievals and models

    NASA Astrophysics Data System (ADS)

    Jiang, Xun; Crisp, David; Olsen, Edward T.; Kulawik, Susan S.; Miller, Charles E.; Pagano, Thomas S.; Liang, Maochang; Yung, Yuk L.

    2016-02-01

    Satellite CO2 retrievals from the Greenhouse gases Observing SATellite (GOSAT), Atmospheric Infrared Sounder (AIRS), and Tropospheric Emission Spectrometer (TES) and in situ measurements from the National Oceanic and Atmospheric Administration - Earth System Research Laboratory (NOAA-ESRL) Surface CO2 and Total Carbon Column Observing Network (TCCON) are utilized to explore the CO2 variability at different altitudes. A multiple regression method is used to calculate the CO2 annual cycle and semiannual cycle amplitudes from different data sets. The CO2 annual cycle and semiannual cycle amplitudes for GOSAT XCO2 and TCCON XCO2 are consistent but smaller than those seen in the NOAA-ESRL surface data. The CO2 annual and semiannual cycles are smallest in the AIRS midtropospheric CO2 compared with other data sets in the Northern Hemisphere. The amplitudes for the CO2 annual cycle and semiannual cycle from GOSAT, TES, and AIRS CO2 are small and comparable to each other in the Southern Hemisphere. Similar regression analysis is applied to the Model for OZone And Related chemical Tracers-2 and CarbonTracker model CO2. The convolved model CO2 annual cycle and semiannual cycle amplitudes are similar to those from the satellite CO2 retrievals, although the models tend to underestimate the CO2 seasonal cycle amplitudes in the Northern Hemisphere midlatitudes and underestimate the CO2 semiannual cycle amplitudes in the high latitudes. These results can be used to better understand the vertical structures for the CO2 annual cycle and semiannual cycle and help identify deficiencies in the models, which are very important for the carbon budget study.

  20. Emission of PCDD/Fs and dioxin-like PCBs from metallurgy industries in S. Korea.

    PubMed

    Yu, Byeong-Woon; Jin, Guang-Zhu; Moon, Young-Hoon; Kim, Min-Kwan; Kyoung, Jong-Dai; Chang, Yoon-Seok

    2006-01-01

    The metallurgy industry and municipal waste incinerators are considered the main sources of polychlorinated dibenzo-p-dioxin and dibenzofurans (PCDD/Fs) in many countries. This study investigated the emission factors and total emissions of PCDD/Fs and dioxin-like polychlorinated biphenyls (PCBs) emitted from metallurgy industries (including ferrous and nonferrous foundries) in Korea. The toxic equivalency (TEQ) emission factor of PCDD/Fs was the highest for secondary copper production, at 24451 ng I-TEQ/ton. The total estimated emissions of PCDD/Fs from these sources were 35.259 g I-TEQ/yr, comprising 0.088 g I-TEQ/yr from ferrous foundries, 31.713 g I-TEQ/yr from copper production, 1.716 g I-TEQ/yr from lead production, 0.111 g I-TEQ/yr from zinc production, and 1.631 g I-TEQ/yr from aluminum production. The total estimated annual amounts of dioxin-like PCBs emitted from these sources were 13.260 g WHO-TEQ/yr, comprising 0.014 g WHO-TEQ/yr from ferrous foundries, 12.675 g WHO-TEQ/yr from copper production, 0.170 g WHO-TEQ/yr from lead production, 0.017 g WHO-TEQ/yr from zinc production, and 0.384 g WHO-TEQ/yr from aluminum production. The highest emission factor was found for secondary copper smelting, at 9770 ng WHO-TEQ/ton.