High DNA stability in white blood cells and buffy coat lysates stored at ambient temperature under anoxic and anhydrous atmosphere.

Directory of Open Access Journals (Sweden)

Anne-Lise Fabre

Full Text Available Conventional storage of blood-derived fractions relies on cold. However, lately, ambient temperature preservation has been evaluated by several independent institutions that see economic and logistic advantages in getting rid of the cold chain. Here we validated a novel procedure for ambient temperature preservation of DNA in white blood cell and buffy coat lysates based on the confinement of the desiccated biospecimens under anoxic and anhydrous atmosphere in original hermetic minicapsules. For this validation we stored encapsulated samples either at ambient temperature or at several elevated temperatures to accelerate aging. We found that DNA extracted from stored samples was of good quality with a yield of extraction as expected. Degradation rates were estimated from the average fragment size of denatured DNA run on agarose gels and from qPCR reactions. At ambient temperature, these rates were too low to be measured but the degradation rate dependence on temperature followed Arrhenius' law, making it possible to extrapolate degradation rates at 25°C. According to these values, the DNA stored in the encapsulated blood products would remain larger than 20 kb after one century at ambient temperature. At last, qPCR experiments demonstrated the compatibility of extracted DNA with routine DNA downstream analyses. Altogether, these results showed that this novel storage method provides an adequate environment for ambient temperature long term storage of high molecular weight DNA in dehydrated lysates of white blood cells and buffy coats.

Continuous determination of gaseous ammonia in the ambient atmosphere using fluorescence derivatization

Science.gov (United States)

Abbas, Rana; Tanner, Roger L.

A method for continuous determination of ambient ammonia levels employing o-phthalaldehyde fluorescence derivatization is described. A simplified Venturi scrubber and gas-liquid separator have been employed for reproducible measurements of ⩾ 0.1 ppb ambient ammonia with less than 2 min time resolution. The scrubbing efficiency of the ammonia gas collection system was determined to be 29 ± 1 %. During 4 d in August 1979 ambient ammonia levels at the Brookhaven National Laboratory site averaged about 1.5 ± 1.1 ppb during afternoon daylight hours.

The contribution of waste water treatment plants to PBDEs in ambient air

International Nuclear Information System (INIS)

Martellini, Tania; Jones, Kevin C.; Sweetman, Andy; Giannoni, Martina; Pieri, Francesca; Cincinelli, Alessandra

2012-01-01

Air samples were collected at different sites in and around two wastewater treatment plants (WWTPs) located in central Italy to determine the concentrations, compositional profiles and contribution to ambient levels of eight polybrominated diphenyl ethers (PBDEs). The investigated WWTPs were selected as they treat industrial wastewater produced by local textile industries along with municipal wastewater. PBDE concentrations within the WWTPs were higher than those measured at reference sites located 4 and 5 km away with BDE-209 dominating the BDE congener composition in all air samples in 2008. Ambient PBDE concentrations measured in and around the WWTPs and estimates of emissions from aeration tanks suggest that WWTPs are sources of PBDEs to ambient air. Principal component analysis and Pearson correlations confirmed this result. The effect of distance from the plant and wind direction on atmospheric concentrations was also investigated. Although the primary fate of PBDEs in WWTPs will be partitioning to sewage sludge, this study suggests that plants can provide a measurable source of these compounds to local ambient air. - Highlights: ► Levels and distribution profiles of PBDEs in the atmosphere surrounding two WWTPs. ► Airborne polybrominated diphenyl ethers in the surrounding area of two WWTPs in Italy. ► To investigate WWTPs as sources of PBDEs to the atmosphere. ► Samples collected downwind respect to the plant showed BDE-209 as dominant congener. ► The effect of distance and wind direction on atmospheric concentrations was also investigated. - Waste water treatment plants as sources of PBDEs to the ambient air.

Atmospheric correction for JPSS-2 VIIRS response versus scan angle measurements

Science.gov (United States)

McIntire, Jeffrey; Moeller, Chris; Oudrari, Hassan; Xiong, Xiaoxiong

2017-09-01

The Joint Polar Satellite System 2 (JPSS-2) Visible Infrared Imaging Radiometer Suite (VIIRS) includes one spectral band centered in a strong atmospheric absorption region. As much of the pre-launch calibration is performed under laboratory ambient conditions, accurately accounting for the absorption, and thereby ensuring the transfer of the sensor calibration to on-orbit operations, is necessary to generate science quality data products. This work is focused on the response versus scan angle (RVS) measurements, which characterize the relative scan angle dependent reflectance of the JPSS-2 VIIRS instrument optics. The spectral band of interest, centered around 1378 nm, is within a spectral region strongly effected by water vapor absorption. The methodology used to model the absolute humidity and the atmospheric transmittance under the laboratory conditions is detailed. The application of this transmittance to the RVS determination is then described including an uncertainty estimate; a comparison to the pre-launch measurements from earlier sensor builds is also performed.

Secondary organic aerosols: Formation potential and ambient data

DEFF Research Database (Denmark)

Barthelmie, R.J.; Pryor, S.C.

1997-01-01

Organic aerosols comprise a significant fraction of the total atmospheric particle loading and are associated with radiative forcing and health impacts. Ambient organic aerosol concentrations contain both a primary and secondary component. Herein, fractional aerosol coefficients (FAC) are used...... in conjunction with measurements of volatile organic compounds (VOC) to predict the formation potential of secondary organic aerosols (SOA) in the Lower Fraser Valley (LEV) of British Columbia. The predicted concentrations of SOA show reasonable accord with ambient aerosol measurements and indicate considerable...

Ten years measuring PCDDs/PCDFs in ambient air in Catalonia (Spain)

Energy Technology Data Exchange (ETDEWEB)

Lluis, G; Gomez, R; Guinart, X; Hernandez, I [Dept. de Medi Ambient de la Generalitat de Catalunya (Spain); Esteban, A; Caixach, J; Manich, A; Rivera, J [Mass Spectrometry Lab., Dept. of Ecotechnologies, IIQAB-CSIC (Spain)

2004-09-15

PCDDs and PCDFs can be formed as unwanted by-products in many anthropogenic processes and their presence in the atmosphere comes mainly from several industrial activities which include, for instance, a variety of thermal processes such as waste management plants, cement kiln plants, sintering plants and other diffuse sources. Furthermore, once released into the atmosphere, these toxicants can be transported far from their original sources and as a result their presence can be determined in remote areas. In this sense, great efforts have been made to increase the knowledge about these pollutants and stringent regulations aiming to protect public health have already been established. Monitoring programs play an important role in public and sanitary decisions. In particular, the presence and trend of this pollutants in the atmosphere have been subject of many environmental studies performed all over the world. In 1994, the Environmental Department (Departament de Medi Ambient) of the Catalonian Government (Generalitat de Catalunya) in collaboration with the Dioxin Laboratory /Mass Spectrometry Laboratory (Dept.of Ecotechnologies) of the Spanish Council for Scientific Research (CSIC) started a surveillance programme on PCDDs/PCDFs in ambient air. The aim of the study was to determine dioxin levels and to assess temporal trends of the atmospheric content of these pollutants in major industrial sites all over Catalonia. Moreover, samples from urban and rural areas as well as other supposedly non-affected sites were also considered. Furthermore, in accordance with the new regulatory framework, a comparison of two different sampling devices, TSP and PM10, has also been performed during the study.

An international marine-atmospheric 222Rn measurement intercomparison in Bermuda. Part 2: Results for the participating laboratories

International Nuclear Information System (INIS)

Colle, R.; Unterweger, M.P.; Hutchinson, J.M.R.

1996-01-01

As part of an international measurement intercomparison of instruments used to measure atmospheric 222 Rn, four participating laboratories made nearly simultaneous measurements of 222 Rn activity concentration in commonly sampled, ambient air over approximately a 2 week period, and three of these four laboratories participated in the measurement comparison of 14 introduced samples with known, but undisclosed (blind) 222 Rn activity concentration. The exercise was conducted in Bermuda in October 1991. The 222 Rn activity concentrations in ambient Bermudian air over the course of the intercomparison ranged from a few hundredths of a Bq · m -3 to about 2 Bq · m -3 , while the standardized sample additions covered a range from approximately 2.5 Bq · m -3 to 35 Bq · m -3 . The overall uncertainty in the latter concentrations was in the general range of 10%, approximating a 3 standard deviation uncertainty interval. The results of the intercomparison indicated that two of the laboratories were within very good agreement with the standard additions, and almost within expected statistical variations. These same two laboratories, however, at lower ambient concentrations, exhibited a systematic difference with an averaged offset of roughly 0.3 Bq · m -3 . The third laboratory participating in the measurement of standardized sample additions was systematically low by about 65% to 70%, with respect to the standard addition which was also confirmed in their ambient air concentration measurements. The fourth laboratory, participating in only the ambient measurement part of the intercomparison, was also systematically low by at least 40% with respect to the first two laboratories

Light-induced magnetoresistance in solution-processed planar hybrid devices measured under ambient conditions.

Science.gov (United States)

Banerjee, Sreetama; Bülz, Daniel; Reuter, Danny; Hiller, Karla; Zahn, Dietrich R T; Salvan, Georgeta

2017-01-01

We report light-induced negative organic magnetoresistance (OMAR) measured in ambient atmosphere in solution-processed 6,13-bis(triisopropylsilylethynyl)pentacene (TIPS-pentacene) planar hybrid devices with two different device architectures. Hybrid electronic devices with trench-isolated electrodes (HED-TIE) having a channel length of ca. 100 nm fabricated in this work and, for comparison, commercially available pre-structured organic field-effect transistor (OFET) substrates with a channel length of 20 µm were used. The magnitude of the photocurrent as well as the magnetoresistance was found to be higher for the HED-TIE devices because of the much smaller channel length of these devices compared to the OFETs. We attribute the observed light-induced negative magnetoresistance in TIPS-pentacene to the presence of electron-hole pairs under illumination as the magnetoresistive effect scales with the photocurrent. The magnetoresistance effect was found to diminish over time under ambient conditions compared to a freshly prepared sample. We propose that the much faster degradation of the magnetoresistance effect as compared to the photocurrent was due to the incorporation of water molecules in the TIPS-pentacene film.

57Fe Moessbauer spectroscopic study on surface products of thin iron plates exposed to ambient atmosphere as a means of environmental monitoring

International Nuclear Information System (INIS)

Matsuo, Motoyuki; Kobayashi, Takaaki

1993-01-01

Conversion electron and transmission Moessbauer spectroscopy were applied to the analysis of thin iron plates exposed to the ambient atmosphere. The degree of corrosion of the iron plates was classified into three categories according to the kind and thickness of rust evaluated by Moessbauer spectra. The severe corrosion took place in seaside and roadside areas. The medium corrosion was observed in urban areas, and the weak corrosion occurred in suburban and mountainous areas. This fact implies that the surface products of iron plates can successfully reflect the ambient atmosphere to which the plates were exposed. (orig.)

Measurements of a potential interference with laser-induced fluorescence measurements of ambient OH from the ozonolysis of biogenic alkenes

Science.gov (United States)

Rickly, Pamela; Stevens, Philip S.

2018-01-01

Reactions of the hydroxyl radical (OH) play a central role in the chemistry of the atmosphere, and measurements of its concentration can provide a rigorous test of our understanding of atmospheric oxidation. Several recent studies have shown large discrepancies between measured and modeled OH concentrations in forested areas impacted by emissions of biogenic volatile organic compounds (BVOCs), where modeled concentrations were significantly lower than measurements. A potential reason for some of these discrepancies involves interferences associated with the measurement of OH using the laser-induced fluorescence-fluorescence assay by gas expansion (LIF-FAGE) technique in these environments. In this study, a turbulent flow reactor operating at atmospheric pressure was coupled to a LIF-FAGE cell and the OH signal produced from the ozonolysis of α-pinene, β-pinene, ocimene, isoprene, and 2-methyl-3-buten-2-ol (MBO) was measured. To distinguish between OH produced from the ozonolysis reactions and any OH artifact produced inside the LIF-FAGE cell, an external chemical scrubbing technique was used, allowing for the direct measurement of any interference. An interference under high ozone (between 2 × 1013 and 10 × 1013 cm-3) and BVOC concentrations (between approximately 0.1 × 1012 and 40 × 1012 cm-3) was observed that was not laser generated and was independent of the ozonolysis reaction time. For the ozonolysis of α- and β-pinene, the observed interference accounted for approximately 40 % of the total OH signal, while for the ozonolysis of ocimene the observed interference accounted for approximately 70 % of the total OH signal. Addition of acetic acid to the reactor eliminated the interference, suggesting that the source of the interference in these experiments involved the decomposition of stabilized Criegee intermediates (SCIs) inside the FAGE detection cell. Extrapolation of these measurements to ambient concentrations suggests that these interferences

Measurement and analysis of ambient atmospheric particulate matter in urban and remote environments

Science.gov (United States)

Hagler, Gayle S. W.

Atmospheric particulate matter pollution is a challenging environmental concern in both urban and remote locations worldwide. It is intrinsically difficult to control, given numerous anthropogenic and natural sources (e.g. fossil fuel combustion, biomass burning, dust, and seaspray) and atmospheric transport up to thousands of kilometers after production. In urban regions, fine particulate matter (particles with diameters under 2.5 mum) is of special concern for its ability to penetrate the human respiratory system and threaten cardiopulmonary health. A second major impact area is climate, with particulate matter altering Earth's radiative balance through scattering and absorbing solar radiation, modifying cloud properties, and reducing surface reflectivity after deposition in snow-covered regions. While atmospheric particulate matter has been generally well-characterized in populated areas of developed countries, particulate pollution in developing nations and remote regions is relatively unexplored. This thesis characterizes atmospheric particulate matter in locations that represent the extreme ends of the spectrum in terms of air pollution-the rapidly-developing and heavily populated Pearl River Delta Region of China, the pristine and climate-sensitive Greenland Ice Sheet, and a remote site in the Colorado Rocky Mountains. In China, fine particles were studied through a year-long field campaign at seven sites surrounding the Pearl River Delta. Fine particulate matter was analyzed for chemical composition, regional variation, and meteorological impacts. On the Greenland Ice Sheet and in the Colorado Rocky Mountains, the carbonaceous fraction (organic and elemental carbon) of particulate matter was studied in the atmosphere and snow pack. Analyses included quantifying particulate chemical and optical properties, assessing atmospheric transport, and evaluating post-depositional processing of carbonaceous species in snow.

Atmospheric nitrogen dioxide at ambient levels stimulates growth and development of horticultural plants

International Nuclear Information System (INIS)

Adam, S.E.H.; Shigeto, J.; Sakamoto, A.; Takahashi, M.; Morikawa, H.

2008-01-01

Studies have demonstrated that ambient levels of atmospheric nitrogen dioxide (NO 2 ) can cause Nicotiana plumbaginifolia to double its biomass as well as its cell contents. This paper examined the influence of NO 2 on lettuce, sunflower, cucumber, and pumpkin plants. Plants were grown in environments supplemented with stable isotope-labelled NO 2 for approximately 6 weeks and irrigated with nitrates. Measured growth parameters included leaf number, internode number, stem length, number of flower buds, and root length. Results of the study demonstrated that the addition of NO 2 doubled the aboveground and belowground biomass of sunflowers, while only the aboveground biomass of pumpkin, cucumbers, and lettuces was doubled. Levels of carbon (C), nitrogen (N), phosphorus (P), potassium (K), calcium (Ca), and magnesium (Mg) were also doubled in the lettuce samples. A mass spectrometry analysis showed that only a small percentage of total plant N was derived from NO 2 . It was concluded that exogenous NO 2 additions function as a signal rather than as a significant nutrient source in horticultural plants. 22 refs., 2 tabs., 1 fig

The NRPI multi-purpose on-line monitoring station for measurement of natural radioactivity in the ambient atmosphere and in the soil

International Nuclear Information System (INIS)

Jilek, K.; Slezakova, M.; Fronka, A.; Prokop, T.; Neubauer, L.

2017-01-01

During years 2010 12 an automated, on-line and wireless outdoor measurement station of atmospheric radon, gamma dose rate and meteorological parameters was realised at the National Radiation Protection Institute (NRPI) in Prague. At the turn of the year 2013 an expansion of the existing station was completed. Under the project funded by the Czech Technological Agency a new updated station was established, additionally equipped with modules for measurement of atmospheric radon/thoron short-lived decay products, radon in water and soil and radon exhalation rate from soil. After the introduction of the station updated key detection parameters and benefits, its use for atmospheric modelling and monitoring is demonstrated. There are summarised results from the 3-year measurement period in the NRPI outdoor area in Prague and from simultaneous annual measurement performed by another similar station located near uranium mud fields in DIAMO, state enterprise, Straz pod Ralskem. Observed seasonal and diurnal variations of atmospheric radon concentrations and variability of the equilibrium factor, F, are illustrated and compared. (authors)

Light-induced magnetoresistance in solution-processed planar hybrid devices measured under ambient conditions

Directory of Open Access Journals (Sweden)

Sreetama Banerjee

2017-07-01

Full Text Available We report light-induced negative organic magnetoresistance (OMAR measured in ambient atmosphere in solution-processed 6,13-bis(triisopropylsilylethynylpentacene (TIPS-pentacene planar hybrid devices with two different device architectures. Hybrid electronic devices with trench-isolated electrodes (HED-TIE having a channel length of ca. 100 nm fabricated in this work and, for comparison, commercially available pre-structured organic field-effect transistor (OFET substrates with a channel length of 20 µm were used. The magnitude of the photocurrent as well as the magnetoresistance was found to be higher for the HED-TIE devices because of the much smaller channel length of these devices compared to the OFETs. We attribute the observed light-induced negative magnetoresistance in TIPS-pentacene to the presence of electron–hole pairs under illumination as the magnetoresistive effect scales with the photocurrent. The magnetoresistance effect was found to diminish over time under ambient conditions compared to a freshly prepared sample. We propose that the much faster degradation of the magnetoresistance effect as compared to the photocurrent was due to the incorporation of water molecules in the TIPS-pentacene film.

Lord Kelvin's atmospheric electricity measurements

Science.gov (United States)

Aplin, Karen; Harrison, R. Giles; Trainer, Matthew; Hough, James

2013-04-01

Lord Kelvin (William Thomson), one of the greatest Victorian scientists, made a substantial but little-recognised contribution to geophysics through his work on atmospheric electricity. He developed sensitive instrumentation for measuring the atmospheric electric field, including invention of a portable electrometer, which made mobile measurements possible for the first time. Kelvin's measurements of the atmospheric electric field in 1859, made during development of the portable electrometer, can be used to deduce the substantial levels of particulate pollution blown over the Scottish island of Arran from the industrial mainland. Kelvin was also testing the electrometer during the largest solar flare ever recorded, the "Carrington event" in the late summer of 1859. Subsequently, Lord Kelvin also developed a water dropper sensor, and employed photographic techniques for "incessant recording" of the atmospheric electric field, which led to the long series of measurements recorded at UK observatories for the remainder of the 19th and much of the 20th century. These data sets have been valuable in both studies of historical pollution and cosmic ray effects on atmospheric processes.

Development, enhancement, and evaluation of aircraft measurement techniques for national ambient air quality standard criteria pollutants

Science.gov (United States)

Brent, Lacey Cluff

The atmospheric contaminants most harmful to human health are designated Criteria Pollutants. To help Maryland attain the national ambient air quality standards (NAAQS) for Criteria Pollutants, and to improve our fundamental understanding of atmospheric chemistry, I conducted aircraft measurements in the Regional Atmospheric Measurement Modeling Prediction Program (RAMMPP). These data are used to evaluate model simulations and satellite observations. I developed techniques for improving airborne observation of two NAAQS pollutants, particulate matter (PM) and nitrogen dioxide (NO2). While structure and composition of organic aerosol are important for understanding PM formation, the molecular speciation of organic ambient aerosol remains largely unknown. The spatial distribution of reactive nitrogen is likewise poorly constrained. To examine water-soluble organic aerosol (WSOA) during an air pollution episode, I designed and implemented a shrouded aerosol inlet system to collect PM onto quartz fiber filters from a Cessna 402 research aircraft. Inlet evaluation conducted during a side-by-side flight with the NASA P3 demonstrated agreement to within 30%. An ion chromatographic mass spectrometric method developed using the NIST Standard Reference Material (SRM) 1649b Urban Dust, as a surrogate material resulted in acidic class separation and resolution of at least 34 organic acids; detection limits approach pg/g concentrations. Analysis of aircraft filter samples resulted in detection of 8 inorganic species and 16 organic acids of which 12 were quantified. Aged, re-circulated metropolitan air showed a greater number of dicarboxylic acids compared to air recently transported from the west. While the NAAQS for NO2 is rarely exceeded, it is a precursor molecule for ozone, America's most recalcitrant pollutant. Using cavity ringdown spectroscopy employing a light emitting diode (LED), I measured vertical profiles of NO2 (surface to 2.5 km) west (upwind) of the Baltimore

Discharge current measurements on Venera 13 & 14 - Evidence for charged aerosols in the Venus lower atmosphere?

Science.gov (United States)

Lorenz, Ralph D.

2018-06-01

Measurements of discharge currents on the Venera 13 and 14 landers during their descent in the lowest 35 km of the Venus atmosphere are interpreted as driven either by an ambient electric field, or by deposition of charge from aerosols. The latter hypothesis is favored (`triboelectric charging' in aeronautical parlance), and would entail an aerosol opacity and charge density somewhat higher than that observed in Saharan dust transported over long distances on Earth.

Characterisation of an inlet pre-injector laser-induced fluorescence instrument for the measurement of atmospheric hydroxyl radicals

Science.gov (United States)

Novelli, A.; Hens, K.; Tatum Ernest, C.; Kubistin, D.; Regelin, E.; Elste, T.; Plass-Dülmer, C.; Martinez, M.; Lelieveld, J.; Harder, H.

2014-10-01

Atmospheric measurements of hydroxyl radicals (OH) are challenging due to a high reactivity and consequently low concentration. The importance of OH as an atmospheric oxidant has motivated a sustained effort leading to the development of a number of highly sensitive analytical techniques. Recent work has indicated that the laser-induced fluorescence of the OH molecules method based on the fluorescence assay by gas expansion technique (LIF-FAGE) for the measurement of atmospheric OH in some environments may be influenced by artificial OH generated within the instrument, and a chemical method to remove this interference was implemented in a LIF-FAGE system by Mao et al. (2012). While it is not clear whether other LIF-FAGE instruments suffer from the same interference, we have applied this method to our LIF-FAGE HORUS (Hydroxyl Radical Measurement Unit based on fluorescence Spectroscopy) system, and developed and deployed an inlet pre-injector (IPI) to determine the chemical zero level in the instrument via scavenging the ambient OH radical. We describe and characterise this technique in addition to its application at field sites in forested locations in Finland, Spain and Germany. Ambient measurements show that OH generated within the HORUS instrument is a non-negligible fraction of the total OH signal, which can comprise 30 to 80% during daytime and 60 to 100% during the night. The contribution of the background OH varied greatly between measurement sites and was likely related to the type and concentration of volatile organic compounds (VOCs) present at each particular location. Two inter-comparisons in contrasting environments between the HORUS instrument and two different chemical ionisation mass spectrometers (CIMS) are described to demonstrate the efficacy of IPI and the necessity of the chemical zeroing method for our LIF-FAGE instrument in such environments.

Conductivity of CH{sub 3}NH{sub 3}PbI{sub 3} thin film perovskite stored in ambient atmosphere

Energy Technology Data Exchange (ETDEWEB)

Gebremichael, Bizuneh, E-mail: bizunehme@gmail.com [Physics Department, Addis Ababa University, Addis Ababa, P.O. Box 1176 (Ethiopia); Alemu, Getachew [Physics Department, Addis Ababa University, Addis Ababa, P.O. Box 1176 (Ethiopia); Tessema Mola, Genene [School of Chemistry & Physics, University of KwaZulu-Nat al, Pietermaritzburg Campus, Private Bag X01, Scottsville 3209 (South Africa)

2017-06-01

Time dependent conductivity loss in CH{sub 3}NH{sub 3}PbI{sub 3} thin film perovskite stored in ambient atmosphere were studied based on electrical and optical measurements. Recent investigations on thin film perovskite solar cell suggest that in the steady state operation of the device, the V{sub oc} is unchanged by continuous illumination of light. Rather the reduction in the power conversion efficiency is caused by significant reduction of the short circuit current (J{sub sc}). In this paper, the effect of light on the optical absorption and electrical conductivity of the CH{sub 3}NH{sub 3}PbI{sub 3} thin film which is deposited on a glass substrate is investigated. The temperature dependent conductivity measurements indicated that the dominant conduction mechanism in the film perovskite is electronic rather than ionic.

Fluxes of CH4 and N2O in aspen stands grown under ambient and twice-ambient CO2

DEFF Research Database (Denmark)

Ambus, P.; Robertson, G.P.

1999-01-01

Elevated atmospheric CO2 has the potential to change below-ground nutrient cycling and thereby alter the soil-atmosphere exchange of biogenic trace gases. We measured fluxes of CH4 and N2O in trembling aspen (Populus tremuloides Michx.) stands grown in open-top chambers under ambient and twice......-ambient CO2 concentrations crossed with `high' and low soil-N conditions. Flux measurements with small static chambers indicated net CH4 oxidation in the open-top chambers. Across dates, CH4 oxidation activity was significantly (P CO2 (8.7 mu g CH4-C m(-2) h(-1)) than...... with elevated CO2 (6.5 mu g CH4-C m(-2) h(-1)) in the low N soil. Likewise, across dates and soil N treatments CH4 was oxidized more rapidly (P CO2 (9.5 mu g CH4-C m(-2) h(-1)) than in chambers with elevated CO2 (8.8 mu g CH4-C m(-2) h(-1)). Methane oxidation in soils incubated...

Atmospheric nitrogen dioxide at ambient levels stimulates growth and development of horticultural plants

Energy Technology Data Exchange (ETDEWEB)

Adam, S.E.H.; Shigeto, J. [Hiroshima Univ., Hiroshima (Japan). Dept. of Mathematical and Life Sciences; Sakamoto, A.; Takahashi, M.; Morikawa, H. [Hiroshima Univ., Hiroshima (Japan). Dept. of Mathematical and Life Sciences, Core Research for Evolutional Science and Technology

2008-02-15

Studies have demonstrated that ambient levels of atmospheric nitrogen dioxide (NO{sub 2}) can cause Nicotiana plumbaginifolia to double its biomass as well as its cell contents. This paper examined the influence of NO{sub 2} on lettuce, sunflower, cucumber, and pumpkin plants. Plants were grown in environments supplemented with stable isotope-labelled NO{sub 2} for approximately 6 weeks and irrigated with nitrates. Measured growth parameters included leaf number, internode number, stem length, number of flower buds, and root length. Results of the study demonstrated that the addition of NO{sub 2} doubled the aboveground and belowground biomass of sunflowers, while only the aboveground biomass of pumpkin, cucumbers, and lettuces was doubled. Levels of carbon (C), nitrogen (N), phosphorus (P), potassium (K), calcium (Ca), and magnesium (Mg) were also doubled in the lettuce samples. A mass spectrometry analysis showed that only a small percentage of total plant N was derived from NO{sub 2}. It was concluded that exogenous NO{sub 2} additions function as a signal rather than as a significant nutrient source in horticultural plants. 22 refs., 2 tabs., 1 fig.

Paloma: In-situ Measurement of The Elemental and Isotopic Composition of The Mars Atmosphere

Science.gov (United States)

Chassefiere, E.; Jambon, A.; Berthelier, J.-J.; Correia, J.-J.; Covinhes, J.; Goulpeau, G.; Leblanc, F.; Malique, Ch.; Sarda, P.; Schaetzel, P.; Sabroux, J.-C.; Ferry, C.; Richon, P.; Pineau, J.-F.; Desjean, M.-C.

The PALOMA instrument, presently under study in the frame of the NASA/CNES Mars exploration program, is devoted to the accurate measurement of isotopic and el- emental ratios in Mars atmosphere. It consists of a mass spectrometer coupled with a gas preparation line for separation of reactive and noble gas species, and noble gas species (and reactive gases) from each other, by chemical and cryogenic trapping, and possibly permeation techniques. This instrument, ranked among the most important four types of measurement recommended by the US Committee on Planetary and Lu- nar Exploration (COMPLEX), will be proposed as a part of the payload of the 07 NASA smart landers. The general objectives of PALOMA are to provide instanta- neous and time-varying patterns of noble gas isotopic spectra, and stable isotopes. Such measurements will allow to improve our general understanding of volatile cy- cles on Mars, and to better decipher the history of the atmosphere and climate. Past escape processes, exchanges between solid planet and atmosphere, post-accretional addition of volatil-rich matter from comets, are expected to have imprinted specific isotopic signatures. Although these signatures are strongly interlocked, a compara- tive Earth-Mars approach may allow to discriminate between them, and therefore to reconstruct the history of Martian volatiles. The evolution of atmospheric mass and composition may have had a major impact on climate evolution, e.g. through massive escape of carbon dioxide and water. In addition, precise measurements of isotopes in the present Mars atmosphere are the most promising way on the short term to confirm that SNC meteorites are from Martian origin. PALOMA also includes a small separate device for measuring ambient natural radioactivity, which might provide information about the presence of a near subsurface permafrost, possible residual volcanic activity, vertical mixing rate in the boundary layer.

A high-resolution mass spectrometer to measure atmospheric ion composition

Directory of Open Access Journals (Sweden)

H. Junninen

2010-08-01

Full Text Available In this paper we present recent achievements on developing and testing a tool to detect the composition of ambient ions in the mass/charge range up to 2000 Th. The instrument is an Atmospheric Pressure Interface Time-of-Flight Mass Spectrometer (APi-TOF, Tofwerk AG. Its mass accuracy is better than 0.002%, and the mass resolving power is 3000 Th/Th. In the data analysis, a new efficient Matlab based set of programs (tofTools were developed, tested and used. The APi-TOF was tested both in laboratory conditions and applied to outdoor air sampling in Helsinki at the SMEAR III station. Transmission efficiency calibrations showed a throughput of 0.1–0.5% in the range 100–1300 Th for positive ions, and linearity over 3 orders of magnitude in concentration was determined. In the laboratory tests the APi-TOF detected sulphuric acid-ammonia clusters in high concentration from a nebulised sample illustrating the potential of the instrument in revealing the role of sulphuric acid clusters in atmospheric new particle formation. The APi-TOF features a high enough accuracy, resolution and sensitivity for the determination of the composition of atmospheric small ions although the total concentration of those ions is typically only 400–2000 cm⁻³. The atmospheric ions were identified based on their exact masses, utilizing Kendrick analysis and correlograms as well as narrowing down the potential candidates based on their proton affinities as well isotopic patterns. In Helsinki during day-time the main negative ambient small ions were inorganic acids and their clusters. The positive ions were more complex, the main compounds were (polyalkyl pyridines and – amines. The APi-TOF provides a near universal interface for atmospheric pressure sampling, and this key feature will be utilized in future laboratory and field studies.

Quantification of Atmospheric Formaldehyde by Near-Infrared Cavity Ring-Down Spectroscopy

Science.gov (United States)

Rella, C.; Hoffnagle, J.; Fleck, D.; Kim-Hak, D.

2017-12-01

Formaldehyde is an important species in atmospheric chemistry, especially in urban environments, where it is a decay product of methane and volatile hydrocarbons. It is also a toxic, carcinogenic compound that can contaminate ambient air from incomplete combustion, or outgassing of commercial products such as adhesives used to fabricate plywood or to affix indoor carpeting. Formaldehyde has a clearly resolved ro-vibrational absorption spectrum that is well-suited to optical analysis of formaldehyde concentration. We describe an instrument based on cavity ring-down spectroscopy for the quantitative analysis of formaldehyde concentration in ambient air. The instrument has a precision (1-sigma) of about 1 ppb at a measurement rate of 1 second, and provides measurements of less than 100 ppt with averaging. The instrument provides stable measurements (drift < 1 ppb) over long periods of time (days). The instrument has been ruggedized for mobile applications, and with a fast response time of a couple of seconds, it is suitable for ground-based vehicle deployments for fenceline monitoring of formaldehyde emissions. In addition, we report on ambient atmospheric measurements at a 10m urban tower, which demonstrate the suitability of the instrument for applications in atmospheric chemistry.

effect of ambient levels of ozone on photosynthetic components

African Journals Online (AJOL)

ACSS

To clarify the long-term effects of ambient levels of tropospheric ozone (O3) on ... (Rubisco), thus contributing to the reduction in net photosynthetic rate at the .... USA). During the measurements, atmospheric. CO2 concentrations, air ...... productivity and implications for climate change. Annual Review of Plant Biology 63:.

Back-exchange: a novel approach to quantifying oxygen diffusion and surface exchange in ambient atmospheres.

Science.gov (United States)

Cooper, Samuel J; Niania, Mathew; Hoffmann, Franca; Kilner, John A

2017-05-17

A novel two-step Isotopic Exchange (IE) technique has been developed to investigate the influence of oxygen containing components of ambient air (such as H 2 O and CO 2 ) on the effective surface exchange coefficient (k*) of a common mixed ionic electronic conductor material. The two step 'back-exchange' technique was used to introduce a tracer diffusion profile, which was subsequently measured using Time-of-Flight Secondary Ion Mass Spectrometry (ToF-SIMS). The isotopic fraction of oxygen in a dense sample as a function of distance from the surface, before and after the second exchange step, could then be used to determine the surface exchange coefficient in each atmosphere. A new analytical solution was found to the diffusion equation in a semi-infinite domain with a variable surface exchange boundary, for the special case where D* and k* are constant for all exchange steps. This solution validated the results of a numerical, Crank-Nicolson type finite-difference simulation, which was used to extract the parameters from the experimental data. When modelling electrodes, D* and k* are important input parameters, which significantly impact performance. In this study La 0.6 Sr 0.4 Co 0.2 Fe 0.8 O 3-δ (LSCF6428) was investigated and it was found that the rate of exchange was increased by around 250% in ambient air compared to high purity oxygen at the same pO 2 . The three experiments performed in this study were used to validate the back-exchange approach and show its utility.

Near-infrared light absorption by brown carbon in the ambient atmosphere

Science.gov (United States)

Chung, C.; Hoffer, A.; Beres, N. D.; Moosmüller, H.; Liu, C.; Green, M.; Kim, S. W.; Engelbrecht, J. P.; Gelencser, A.

2017-12-01

Organic aerosols have been assumed to have little-to-no absorption in the red and near-infrared spectral regions of solar radiation, even though a class of organic aerosols were shown to absorb significantly in these spectral regions. Here, we show that ambient atmospheric data from commonly-used 7-wavelength aethalometers contain evidence of abundant near-infrared light absorption by organic aerosol. This evidence comes from the absorption Ångström exponent over 880 950 nm, which often exceeds values explainable by fresh or coated black carbon, or mineral dust. This evidence is not due to an artifact from the instrument random errors or biases, either. The best explanation for these large 880/950 nm absorption Ångström exponent values in the aethalometer data is near-infrared light absorption by tar balls. Tar balls are among common particles from forest fire.

Uncertainty associated with the gravimetric measurement of particulate matter concentration in ambient air.

Science.gov (United States)

Lacey, Ronald E; Faulkner, William Brock

2015-07-01

This work applied a propagation of uncertainty method to typical total suspended particulate (TSP) sampling apparatus in order to estimate the overall measurement uncertainty. The objectives of this study were to estimate the uncertainty for three TSP samplers, develop an uncertainty budget, and determine the sensitivity of the total uncertainty to environmental parameters. The samplers evaluated were the TAMU High Volume TSP Sampler at a nominal volumetric flow rate of 1.42 m3 min(-1) (50 CFM), the TAMU Low Volume TSP Sampler at a nominal volumetric flow rate of 17 L min(-1) (0.6 CFM) and the EPA TSP Sampler at the nominal volumetric flow rates of 1.1 and 1.7 m3 min(-1) (39 and 60 CFM). Under nominal operating conditions the overall measurement uncertainty was found to vary from 6.1x10(-6) g m(-3) to 18.0x10(-6) g m(-3), which represented an uncertainty of 1.7% to 5.2% of the measurement. Analysis of the uncertainty budget determined that three of the instrument parameters contributed significantly to the overall uncertainty: the uncertainty in the pressure drop measurement across the orifice meter during both calibration and testing and the uncertainty of the airflow standard used during calibration of the orifice meter. Five environmental parameters occurring during field measurements were considered for their effect on overall uncertainty: ambient TSP concentration, volumetric airflow rate, ambient temperature, ambient pressure, and ambient relative humidity. Of these, only ambient TSP concentration and volumetric airflow rate were found to have a strong effect on the overall uncertainty. The technique described in this paper can be applied to other measurement systems and is especially useful where there are no methods available to generate these values empirically. This work addresses measurement uncertainty of TSP samplers used in ambient conditions. Estimation of uncertainty in gravimetric measurements is of particular interest, since as ambient particulate

Effects of ambient temperature and water vapor on chamber pressure and oxygen level during low atmospheric pressure stunning of poultry.

Science.gov (United States)

Holloway, Paul H; Pritchard, David G

2017-08-01

The characteristics of the vacuum used in a low atmospheric pressure stunning system to stun (render unconscious) poultry prior to slaughter are described. A vacuum chamber is pumped by a wet screw compressor. The vacuum pressure is reduced from ambient atmospheric pressure to an absolute vacuum pressure of ∼250 Torr (∼33 kPa) in ∼67 sec with the vacuum gate valve fully open. At ∼250 Torr, the sliding gate valve is partially closed to reduce effective pumping speed, resulting in a slower rate of decreasing pressure. Ambient temperature affects air density and water vapor pressure and thereby oxygen levels and the time at the minimum total pressure of ∼160 Torr (∼21 kPa) is varied from ∼120 to ∼220 sec to ensure an effective stun within the 280 seconds of each cycle. The reduction in total pressure results in a gradual reduction of oxygen partial pressure that was measured by a solid-state electrochemical oxygen sensor. The reduced oxygen pressure leads to hypoxia, which is recognized as a humane method of stunning poultry. The system maintains an oxygen concentration of air always reduces the oxygen concentrations to a value lower than in dry air. The partial pressure of water and oxygen were found to depend on the pump down parameters due to the formation of fog in the chamber and desorption of water from the birds and the walls of the vacuum chamber. © The Author 2017. Published by Oxford University Press on behalf of Poultry Science Association.

Airborne Atmospheric Aerosol Measurement System

Science.gov (United States)

Ahn, K.; Park, Y.; Eun, H.; Lee, H.

2015-12-01

It is important to understand the atmospheric aerosols compositions and size distributions since they greatly affect the environment and human health. Particles in the convection layer have been a great concern in global climate changes. To understand these characteristics satellite, aircraft, and radio sonde measurement methods have usually been used. An aircraft aerosol sampling using a filter and/or impactor was the method commonly used (Jay, 2003). However, the flight speed particle sampling had some technical limitations (Hermann, 2001). Moreover, the flight legal limit, altitude, prohibited airspace, flight time, and cost was another demerit. To overcome some of these restrictions, Tethered Balloon Package System (T.B.P.S.) and Recoverable Sonde System(R.S.S.) were developed with a very light optical particle counter (OPC), impactor, and condensation particle counter (CPC). Not only does it collect and measure atmospheric aerosols depending on altitudes, but it also monitors the atmospheric conditions, temperature, humidity, wind velocity, pressure, GPS data, during the measurement (Eun, 2013). In this research, atmospheric aerosol measurement using T.B.P.S. in Ansan area is performed and the measurement results will be presented. The system can also be mounted to an unmanned aerial vehicle (UAV) and create an aerial particle concentration map. Finally, we will present measurement data using Tethered Balloon Package System (T.B.P.S.) and R.S.S (Recoverable Sonde System).

Some measurements of ambient air pollution

International Nuclear Information System (INIS)

Memon, H.R.; Memon, A.A.; Behan, M.Y.

1999-01-01

Ambient air pollution arising from different sources in Karachi and its surroundings has been studied. The urban centres like Karachi are mostly confronted with eye-irritation, reduce visibility, heart-diseases, nervous disorder, smog and other unpleasant experiences. In this paper quantitative estimations of some air-pollutants such as sulphur dioxide, carbon monoxide, oxides of nitrogen, chlorine and particular matters are presented with their hazardous effects. The remedial measures for the control of major air emissions are also discussed. (author)

Global Atmosphere Watch Workshop on Measurement-Model ...

Science.gov (United States)

The World Meteorological Organization’s (WMO) Global Atmosphere Watch (GAW) Programme coordinates high-quality observations of atmospheric composition from global to local scales with the aim to drive high-quality and high-impact science while co-producing a new generation of products and services. In line with this vision, GAW’s Scientific Advisory Group for Total Atmospheric Deposition (SAG-TAD) has a mandate to produce global maps of wet, dry and total atmospheric deposition for important atmospheric chemicals to enable research into biogeochemical cycles and assessments of ecosystem and human health effects. The most suitable scientific approach for this activity is the emerging technique of measurement-model fusion for total atmospheric deposition. This technique requires global-scale measurements of atmospheric trace gases, particles, precipitation composition and precipitation depth, as well as predictions of the same from global/regional chemical transport models. The fusion of measurement and model results requires data assimilation and mapping techniques. The objective of the GAW Workshop on Measurement-Model Fusion for Global Total Atmospheric Deposition (MMF-GTAD), an initiative of the SAG-TAD, was to review the state-of-the-science and explore the feasibility and methodology of producing, on a routine retrospective basis, global maps of atmospheric gas and aerosol concentrations as well as wet, dry and total deposition via measurement-model

Ambient dose measurement in some CT departments in Khartoum State

International Nuclear Information System (INIS)

Mohammed, S. A. H.

2012-09-01

Computerized Tomography (CT) is now one of the most important radiological examinations world wide.The frequency of CT examinations is increasing rapidly from 2% of all radiological examinations in some countries a decade age to 10-15% now. During the imaging procedure, staff may expose to a significant dose. Therefore, ambient dose measurement is important in the shortage of regular personal monitoring in sudan. This study intended to evaluate the ambient dose at some CT departments (Medical Military hospital, Alamal National Hospital, Elnelin Diagnostic Center and Modern Medical Centre). These departments were equipped with daul, 16 and 64 multi detector CT machines. A survey meter (Radios) was used to measure ambient doses in three locations: Doors, Control Rooms and Adjacent Rooms. The ambient dose equivalent (scatter dose) was measured at various distances from the isocenter of the CT unit at various angles to establish isodose cartography. The mean and range of radiation at control room is 10.00-0.20 and mean (7.05μSv/hr,) reception 1.0-0 (0.40) and doors 4.00-100.00 (73.5) for height 1 meter above the ground. For height 2 meters at control room 0-10.00 (6,75), reception 0-90.00 (30) at door 9.00-90.00 (49.50). This study confirms that low levels of radiation dose are received by staff during CT imaging and these levels are within safe limits as prescribed by the national and international regulations. (Author)

Remote sensing FTIR-system for emission monitoring and ambient air control of atmospheric trace gases and air pollutants; Remote sensing FTIR-System zur Emissions- und Immissionsmessung atmosphaerischer Spurengasse und Luftschadstoffe

Energy Technology Data Exchange (ETDEWEB)

Eisenmann, T; Mosebach, H; Bittner, H [Kayser-Threde GmbH, Muenchen (Germany)

1994-01-01

The Fourier Transform Infrared spectrometer K300, based on the double-pendulum interferometer, is due to its optical design particularly suitable for high resolution remote sensing emission and transmission (long path monitoring) measurements of air pollutants and atmospheric trace gases in the field. The applications encompass direct emission measurements of hot flue gases and aircraft engine exhaust as well as surveillance of industrial complexes and waste disposal sites and ambient air control of e.g. traffic polluted sites. For direct emission measurements the infrared radiation of hot gases is utilized. Monitoring of cold diffuse emissions (e.g. at waste disposal sites) and ambient air control is carried out applying a bistatic transmission configuration with an artificial infrared source (glowbar) facing the instrument from a distance up to several hundred meters (long-path monitoring). Following a short introduction of the measurement technique and system, results from the above mentioned applications, obtained during several field studies are depicted and discussed. 19 refs., 8 figs., 12 tabs.

Remote measurement of atmospheric pollutants

Science.gov (United States)

Allario, F.; Hoell, J.; Seals, R. K.

1979-01-01

The concentration and vertical distribution of atmospheric ammonia and ozone are remotely sensed, using dual-C02-laser multichannel infrared Heterodyne Spectrometer (1HS). Innovation makes atmospheric pollution measurements possible with nearly-quantum-noise-limited sensitivity and ultrafine spectral resolution.

Innovative measurement within the atmosphere of Venus.

Science.gov (United States)

Ekonomov, Alexey; Linkin, Vyacheslav; Manukin, Anatoly; Makarov, Vladislav; Lipatov, Alexander

The results of Vega project experiments with two balloons flew in the cloud layer of the atmosphere of Venus are analyzed as to the superrotation nature and local dynamic and thermodynamic characteristics of the atmosphere. These balloons in conjunction with measurements of temperature profiles defined by the Fourier spectrometer measurements from the spacecraft Venera 15 allow us to offer a mechanism accelerating the atmosphere to high zonal velocities and supporting these speeds, the atmosphere superrotation in general. Spectral measurements with balloons confirm the possibility of imaging the planet's surface from a height of not more than 55 km. Promising experiments with balloons in the atmosphere of Venus are considered. In particular, we discuss the possibility of measuring the geopotential height, as Venus no seas and oceans to vertical positioning of the temperature profiles. As an innovative research facilities within the atmosphere overpressure balloon with a lifetime longer than 14 Earth days and vertical profile microprobes are considered.

Mobile Communication Devices, Ambient Noise, and Acoustic Voice Measures.

Science.gov (United States)

Maryn, Youri; Ysenbaert, Femke; Zarowski, Andrzej; Vanspauwen, Robby

2017-03-01

The ability to move with mobile communication devices (MCDs; ie, smartphones and tablet computers) may induce differences in microphone-to-mouth positioning and use in noise-packed environments, and thus influence reliability of acoustic voice measurements. This study investigated differences in various acoustic voice measures between six recording equipments in backgrounds with low and increasing noise levels. One chain of continuous speech and sustained vowel from 50 subjects with voice disorders (all separated by silence intervals) was radiated and re-recorded in an anechoic chamber with five MCDs and one high-quality recording system. These recordings were acquired in one condition without ambient noise and in four conditions with increased ambient noise. A total of 10 acoustic voice markers were obtained in the program Praat. Differences between MCDs and noise condition were assessed with Friedman repeated-measures test and posthoc Wilcoxon signed-rank tests, both for related samples, after Bonferroni correction. (1) Except median fundamental frequency and seven nonsignificant differences, MCD samples have significantly higher acoustic markers than clinical reference samples in minimal environmental noise. (2) Except median fundamental frequency, jitter local, and jitter rap, all acoustic measures on samples recorded with the reference system experienced significant influence from room noise levels. Fundamental frequency is resistant to recording system, environmental noise, and their combination. All other measures, however, were impacted by both recording system and noise condition, and especially by their combination, often already in the reference/baseline condition without added ambient noise. Caution is therefore warranted regarding implementation of MCDs as clinical recording tools, particularly when applied for treatment outcomes assessments. Copyright © 2017 The Voice Foundation. Published by Elsevier Inc. All rights reserved.

Atmospheric Measurements Laboratory (AML)

Data.gov (United States)

Federal Laboratory Consortium — The Atmospheric Measurements Laboratory (AML) is one of the nation's leading research facilities for understanding aerosols, clouds, and their interactions. The AML...

Characterization of the natural ambient sound environment : Measurements in open agricultural grassland

NARCIS (Netherlands)

Boersma, HF

The audibility of manmade sound in a natural environment is affected because of masking by ambient sound. In this report results are presented of measurements of the level and spectral composition of natural ambient sound. The statistical L-95 level was determined, i.e., the sound pressure level

Arctic summertime measurements of ammonia in the near-surface atmosphere

Science.gov (United States)

Moravek, A.; Murphy, J. G.; Wentworth, G.; Croft, B.; Martin, R.

2016-12-01

Measurements of gas-phase ammonia (NH3) in the summertime Arctic are rare, despite the impact NH3 can have on new particle formation rates and nitrogen deposition. The presence of NH3 can also increase the ratio of particulate-phase ammonium (NH4+) to non-sea salt sulphate (nss-SO42-) which decreases particle acidity. Known regional sources of NH3in the Arctic summertime include migratory seabird colonies and northern wildfires, whereas the Arctic Ocean is a net sink. In the summer of 2016, high time resolution measurements were collected in the Arctic to improve our understanding of the sources, sinks and impacts of ammonia in this remote region. A four week study was conducted at Alert, Canada (82.5º N, 62.3 º W) from June 23 to July 19, 2016 to examine the magnitude and sources of NH3 and SO42-. The Ambient Ion Monitor-Ion Chromatography system (AIM-IC) provided on-line, hourly averaged measurements of NH3, NH4+, SO42- and Na+. Measurements of NH3 ranged between 50 and 700 pptv (campaign mean of 240 pptv), consistent with previous studies in the summertime Arctic boundary layer. Levels of NH4+ and nss-SO42- were near or below detection limits ( 20 ng m-3) for the majority of the study. Tundra and lake samples were collected to investigate whether these could be important local sources of NH3 at Alert. These surface samples were analyzed for NH4+, pH and temperature and a compensation point (χ) for each sample was calculated to determine if these surface reservoirs can act as net NH3 sources. Precipitation samples were also collected throughout the study to better constrain our understanding of wet NH4+deposition in the summertime Arctic. From mid-July through August, 2016, NH3 was measured continuously using a laser spectroscopy technique onboard the Canadian Coast Guard Ship Amundsen in the eastern Arctic Ocean. Ocean-atmosphere exchange of NH3 was quantified using measurements of sea surface marine NH4+ concentrations. In addition, wet deposition of

Influence of low ambient temperature on epitympanic temperature measurement: a prospective randomized clinical study.

Science.gov (United States)

Strapazzon, Giacomo; Procter, Emily; Putzer, Gabriel; Avancini, Giovanni; Dal Cappello, Tomas; Überbacher, Norbert; Hofer, Georg; Rainer, Bernhard; Rammlmair, Georg; Brugger, Hermann

2015-11-05

Epitympanic temperature (Tty) measured with thermistor probes correlates with core body temperature (Tcore), but the reliability of measurements at low ambient temperature is unknown. The aim of this study was to determine if commercially-available thermistor-based Tty reflects Tcore in low ambient temperature and if Tty is influenced by insulation of the ear. Thirty-one participants (two females) were exposed to room (23.2 ± 0.4 °C) and low (-18.7 ± 1.0 °C) ambient temperature for 10 min using a randomized cross-over design. Tty was measured using an epitympanic probe (M1024233, GE Healthcare Finland Oy) and oesophageal temperature (Tes) with an oesophageal probe (M1024229, GE Healthcare Finland Oy) inserted into the lower third of the oesophagus. Ten participants wore ear protectors (Arton 2200, Emil Lux GmbH & Co. KG, Wermelskirchen, Switzerland) to insulate the ear from ambient air. During exposure to room temperature, mean Tty increased from 33.4 ± 1.5 to 34.2 ± 0.8 °C without insulation of the ear and from 35.0 ± 0.8 to 35.5 ± 0.7 °C with insulation. During exposure to low ambient temperature, mean Tty decreased from 32.4 ± 1.6 to 28.5 ± 2.0 °C without insulation and from 35.6 ± 0.6 to 35.2 ± 0.9 °C with insulation. The difference between Tty and Tes at low ambient temperature was reduced by 82% (from 7.2 to 1.3 °C) with insulation of the ear. Epitympanic temperature measurements are influenced by ambient temperature and deviate from Tes at room and low ambient temperature. Insulating the ear with ear protectors markedly reduced the difference between Tty and Tes and improved the stability of measurements. The use of models to correct Tty may be possible, but results should be validated in larger studies.

Atmospheric corrosion in Gran Canaria specifically meteorological and pollution conditions

International Nuclear Information System (INIS)

Gonzalez, J.E.G.; Valles, M.L.; Mirza R, J.C.

1998-01-01

Carbon steel, copper, zinc and aluminium samples were exposed in different sizes with known ambient parameters in Gran Canaria Island and atmospheric corrosion was investigated. Weight-loss measurements used to determine corrosion damage were complemented with metallographic and XP S determination in order to characterize the structure and morphology of surface corrosion products. The ambient aggressiveness could be well evaluated from meteorological and pollution data. All atmospheric corrosion and environmental data were statistically processed for establishing general corrosion damage functions for carbon steel, copper, aluminium and zinc in terms of Gran Canaria extreme meteorological and pollution parameters. (Author)

Mobile Instruments Measure Atmospheric Pollutants

Science.gov (United States)

2009-01-01

As a part of NASA's active research of the Earth s atmosphere, which has included missions such as the Atmospheric Laboratory of Applications and Science (ATLAS, launched in 1992) and the Total Ozone Mapping Spectrometer (TOMS, launched on the Earth Probe satellite in 1996), the Agency also performs ground-based air pollution research. The ability to measure trace amounts of airborne pollutants precisely and quickly is important for determining natural patterns and human effects on global warming and air pollution, but until recent advances in field-grade spectroscopic instrumentation, this rapid, accurate data collection was limited and extremely difficult. In order to understand causes of climate change and airborne pollution, NASA has supported the development of compact, low power, rapid response instruments operating in the mid-infrared "molecular fingerprint" portion of the electromagnetic spectrum. These instruments, which measure atmospheric trace gases and airborne particles, can be deployed in mobile laboratories - customized ground vehicles, typically - to map distributions of pollutants in real time. The instruments must be rugged enough to operate rapidly and accurately, despite frequent jostling that can misalign, damage, or disconnect sensitive components. By measuring quickly while moving through an environment, a mobile laboratory can correlate data and geographic points, revealing patterns in the environment s pollutants. Rapid pollutant measurements also enable direct determination of pollutant sources and sinks (mechanisms that remove greenhouse gases and pollutants), providing information critical to understanding and managing atmospheric greenhouse gas and air pollutant concentrations.

Characteristics of Ambient Volatile Organic Compounds (VOCs Measured in Shanghai, China

Directory of Open Access Journals (Sweden)

Guang-Qiang Zhou

2010-08-01

Full Text Available To better understand the characteristics of ambient abundance of volatile organic compounds (VOCs in Shanghai, one of the biggest metropolis of China, VOCs were measured with a gas chromatography system equipped with a mass-selective detector (GC/MSD from July 2006 to February 2010. An intensive measurement campaign was conducted (eight samples per day with a 3 hour interval during May 2009. The comparison of ambient VOCs collected in different regions of Shanghai shows that the concentrations are slightly higher in the busy commercial area (28.9 ppbv at Xujiaui than in the urban administrative area (24.3 ppbv at Pudong. However, during the intensive measurement period, the concentrations in the large steel industrial area (28.7 ppbv at Baoshan were much higher than in the urban administrative area (18 ppbv at Pudong, especially for alkanes, alkenes, and toluene. The seasonal variations of ambient VOC concentrations measured at the Xujiahui sampling site indicate that the VOC concentrations are significantly affected by meteorological conditions (such as wind direction and precipitation. In addition, although alkanes are the most abundant VOCs at the Xujiahui measurement site, the most important VOCs contributing to ozone formation potential (OFP are aromatics, accounting for 57% of the total OFP. The diurnal variations of VOC concentrations show that VOC concentrations are higher on weekdays than in weekends at the Xujiahui sampling site, suggesting that traffic condition and human activities have important impacts on VOC emissions in Shanghai. The evidence also shows that the major sources of isoprene are mainly resulted from gasoline evaporation at a particular time (06:00–09:00 in the busy commercial area. The results gained from this study provide useful information for better understanding the characteristics of ambient VOCs and the sources of VOCs in Shanghai.

Characteristics of Ambient Volatile Organic Compounds (VOCs) Measured in Shanghai, China

Science.gov (United States)

Cai, Chang-Jie; Geng, Fu-Hai; Tie, Xue-Xi; Yu, Qiong; Peng, Li; Zhou, Guang-Qiang

2010-01-01

To better understand the characteristics of ambient abundance of volatile organic compounds (VOCs) in Shanghai, one of the biggest metropolis of China, VOCs were measured with a gas chromatography system equipped with a mass-selective detector (GC/MSD) from July 2006 to February 2010. An intensive measurement campaign was conducted (eight samples per day with a 3 hour interval) during May 2009. The comparison of ambient VOCs collected in different regions of Shanghai shows that the concentrations are slightly higher in the busy commercial area (28.9 ppbv at Xujiaui) than in the urban administrative area (24.3 ppbv at Pudong). However, during the intensive measurement period, the concentrations in the large steel industrial area (28.7 ppbv at Baoshan) were much higher than in the urban administrative area (18 ppbv at Pudong), especially for alkanes, alkenes, and toluene. The seasonal variations of ambient VOC concentrations measured at the Xujiahui sampling site indicate that the VOC concentrations are significantly affected by meteorological conditions (such as wind direction and precipitation). In addition, although alkanes are the most abundant VOCs at the Xujiahui measurement site, the most important VOCs contributing to ozone formation potential (OFP) are aromatics, accounting for 57% of the total OFP. The diurnal variations of VOC concentrations show that VOC concentrations are higher on weekdays than in weekends at the Xujiahui sampling site, suggesting that traffic condition and human activities have important impacts on VOC emissions in Shanghai. The evidence also shows that the major sources of isoprene are mainly resulted from gasoline evaporation at a particular time (06:00–09:00) in the busy commercial area. The results gained from this study provide useful information for better understanding the characteristics of ambient VOCs and the sources of VOCs in Shanghai. PMID:22163629

Measuring method to impulse neutron scattering background in complicated ambient condition

International Nuclear Information System (INIS)

Tang Zhangkui; Peng Taiping; Tang Zhengyuan; Liu Hangang; Hu Mengchun; Fan Juan

2004-01-01

This paper introduced a measuring method and calculative formula about impulse neutron scattering background in complicated ambient condition. The experiment had been done in the lab, and the factors to affect measurement conclusion were analysised. (authors)

A method to measure internal stray radiation of cryogenic infrared imaging systems under various ambient temperatures

Science.gov (United States)

Tian, Qijie; Chang, Songtao; Li, Zhou; He, Fengyun; Qiao, Yanfeng

2017-03-01

The suppression level of internal stray radiation is a key criterion for infrared imaging systems, especially for high-precision cryogenic infrared imaging systems. To achieve accurate measurement for internal stray radiation of cryogenic infrared imaging systems under various ambient temperatures, a measurement method, which is based on radiometric calibration, is presented in this paper. First of all, the calibration formula is deduced considering the integration time, and the effect of ambient temperature on internal stray radiation is further analyzed in detail. Then, an approach is proposed to measure the internal stray radiation of cryogenic infrared imaging systems under various ambient temperatures. By calibrating the system under two ambient temperatures, the quantitative relation between the internal stray radiation and the ambient temperature can be acquired, and then the internal stray radiation of the cryogenic infrared imaging system under various ambient temperatures can be calculated. Finally, several experiments are performed in a chamber with controllable inside temperatures to evaluate the effectiveness of the proposed method. Experimental results indicate that the proposed method can be used to measure internal stray radiation with high accuracy at various ambient temperatures and integration times. The proposed method has some advantages, such as simple implementation and the capability of high-precision measurement. The measurement results can be used to guide the stray radiation suppression and to test whether the internal stray radiation suppression performance meets the requirement or not.

A reaction cell for ambient pressure soft x-ray absorption spectroscopy

Science.gov (United States)

Castán-Guerrero, C.; Krizmancic, D.; Bonanni, V.; Edla, R.; Deluisa, A.; Salvador, F.; Rossi, G.; Panaccione, G.; Torelli, P.

2018-05-01

We present a new experimental setup for performing X-ray Absorption Spectroscopy (XAS) in the soft X-ray range at ambient pressure. The ambient pressure XAS setup is fully compatible with the ultra high vacuum environment of a synchrotron radiation spectroscopy beamline end station by means of ultrathin Si3N4 membranes acting as windows for the X-ray beam and seal of the atmospheric sample environment. The XAS detection is performed in total electron yield (TEY) mode by probing the drain current from the sample with a picoammeter. The high signal/noise ratio achievable in the TEY mode, combined with a continuous scanning of the X-ray energies, makes it possible recording XAS spectra in a few seconds. The first results show the performance of this setup to record fast XAS spectra from sample surfaces exposed at atmospheric pressure, even in the case of highly insulating samples. The use of a permanent magnet inside the reaction cell enables the measurement of X-ray magnetic circular dichroism at ambient pressure.

What metrology can do to improve the quality of your atmospheric ammonia measurements

Science.gov (United States)

Leuenberger, Daiana; Martin, Nicholas A.; Pascale, Céline; Guillevic, Myriam; Ackermann, Andreas; Ferracci, Valerio; Cassidy, Nathan; Hook, Josh; Battersby, Ross M.; Tang, Yuk S.; Stevens, Amy C. M.; Jones, Matthew R.; Braban, Christine F.; Gates, Linda; Hangartner, Markus; Sacco, Paolo; Pagani, Diego; Hoffnagle, John A.; Niederhauser, Bernhard

2017-04-01

Measuring ammonia in ambient air is a sensitive and priority issue due to its harmful effects on human health and ecosystems. The European Directive 2001/81/EC on "National Emission Ceilings for Certain Atmospheric Pollutants (NEC)" regulates ammonia emissions in the member states. However, there is a lack of regulation to ensure reliable ammonia measurements, namely in applicable analytical technology, maximum allowed uncertainty, quality assurance and quality control (QC/QA) procedures, as well as in the infrastructure to attain metrological traceability, i.e. that the results of measurements are traceable to SI-units through an unbroken chain of calibrations. In the framework of the European Metrology Research Programme (EMRP) project on the topic "Metrology for Ammonia in Ambient Air" (MetNH3), European national metrology institutes (NMI's) have joined to tackle the issue of generating SI-traceable reference material, i.e. generate reference gas mixtures containing known amount fractions of NH3.This requires special infrastructure and analytical techniques: Measurements of ambient ammonia are commonly carried out with diffusive samplers or by active sampling with denuders, but such techniques have not yet been extensively validated. Improvements in the metrological traceability may be achieved through the determination of NH3 diffusive sampling rates using ammonia Primary Standard Gas Mixtures (PSMs), developed by gravimetry at the National Physical Laboratory NPL and a controlled atmosphere test facility in combination with on-line monitoring with a cavity ring-down spectrometer. The Federal Institute of Metrology METAS has developed an infrastructure to generate SI-traceable NH3 reference gas mixtures dynamically in the amount fraction range 0.5-500 nmol/mol (atmospheric concentrations) and with uncertainties UNH3 mobile device for full flexibility for calibrations in the laboratory and in the field. Both devices apply the method of temperature and pressure

Volatility measurement of atmospheric submicron aerosols in an urban atmosphere in southern China

Science.gov (United States)

Cao, Li-Ming; Huang, Xiao-Feng; Li, Yuan-Yuan; Hu, Min; He, Ling-Yan

2018-02-01

Aerosol pollution has been a very serious environmental problem in China for many years. The volatility of aerosols can affect the distribution of compounds in the gas and aerosol phases, the atmospheric fates of the corresponding components, and the measurement of the concentration of aerosols. Compared to the characterization of chemical composition, few studies have focused on the volatility of aerosols in China. In this study, a thermodenuder aerosol mass spectrometer (TD-AMS) system was deployed to study the volatility of non-refractory submicron particulate matter (PM1) species during winter in Shenzhen. To our knowledge, this paper is the first report of the volatilities of aerosol chemical components based on a TD-AMS system in China. The average PM1 mass concentration during the experiment was 42.7±20.1 µg m-3, with organic aerosol (OA) being the most abundant component (43.2 % of the total mass). The volatility of chemical species measured by the AMS varied, with nitrate showing the highest volatility, with a mass fraction remaining (MFR) of 0.57 at 50 °C. Organics showed semi-volatile characteristics (the MFR was 0.88 at 50 °C), and the volatility had a relatively linear correlation with the TD temperature (from the ambient temperature to 200 °C), with an evaporation rate of 0.45 % °C-1. Five subtypes of OA were resolved from total OA using positive matrix factorization (PMF) for data obtained under both ambient temperature and high temperatures through the TD, including a hydrocarbon-like OA (HOA, accounting for 13.5 %), a cooking OA (COA, 20.6 %), a biomass-burning OA (BBOA, 8.9 %), and two oxygenated OAs (OOAs): a less-oxidized OOA (LO-OOA, 39.1 %) and a more-oxidized OOA (MO-OOA, 17.9 %). Different OA factors presented different volatilities, and the volatility sequence of the OA factors at 50 °C was HOA (MFR of 0.56) > LO-OOA (0.70) > COA (0.85) ≈ BBOA (0.87) > MO-OOA (0.99), which was not completely consistent with the sequence of their O

Dispersion of effluents in the atmosphere; Dispersion des effluents dans l`atmosphere

Energy Technology Data Exchange (ETDEWEB)

NONE

1999-12-31

This conference day was organized by the `convection` section of the French association of thermal engineers with the support of the environment and energy mastery agency (ADEME). This book of proceedings contains 10 papers entitled: `physical modeling of atmospheric dispersion in wind tunnels. Some industrial examples`; `modeling of the noxious effects of a fire on the environment of an industrial site: importance of thermal engineering related hypotheses`; `atmospheric diffusion of a noxious cloud: fast evaluation method of safety areas around refrigerating installations that use ammonia`; `modeling of atmospheric flows in urban areas in order to study the dispersion of pollutants`; `use of a dispersion parameter to characterize the evolution of a diffusion process downstream of a linear source of passive contaminant placed inside a turbulent boundary layer`; `elements of reflexion around the development of an analytical methodology applied to the elaboration of measurement strategies of air quality in ambient and outdoor atmospheres around industrial sites`; `state-of-the-art about treatment techniques for VOC-rich gaseous effluents`; `characteristics of the time variation of the atmospheric pollution in the Paris region and visualization of its space distribution`; `mass-spectrometry for the measurement of atmospheric pollutants`; `volume variations in natural convection turbulence`. (J.S.)

Dispersion of effluents in the atmosphere; Dispersion des effluents dans l`atmosphere

Energy Technology Data Exchange (ETDEWEB)

NONE

1998-12-31

This conference day was organized by the `convection` section of the French association of thermal engineers with the support of the environment and energy mastery agency (ADEME). This book of proceedings contains 10 papers entitled: `physical modeling of atmospheric dispersion in wind tunnels. Some industrial examples`; `modeling of the noxious effects of a fire on the environment of an industrial site: importance of thermal engineering related hypotheses`; `atmospheric diffusion of a noxious cloud: fast evaluation method of safety areas around refrigerating installations that use ammonia`; `modeling of atmospheric flows in urban areas in order to study the dispersion of pollutants`; `use of a dispersion parameter to characterize the evolution of a diffusion process downstream of a linear source of passive contaminant placed inside a turbulent boundary layer`; `elements of reflexion around the development of an analytical methodology applied to the elaboration of measurement strategies of air quality in ambient and outdoor atmospheres around industrial sites`; `state-of-the-art about treatment techniques for VOC-rich gaseous effluents`; `characteristics of the time variation of the atmospheric pollution in the Paris region and visualization of its space distribution`; `mass-spectrometry for the measurement of atmospheric pollutants`; `volume variations in natural convection turbulence`. (J.S.)

Stable isotope measurements of atmospheric CO2

International Nuclear Information System (INIS)

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

2002-01-01

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

Measurements and simulations of the radiation exposure to aircraft crew workplaces due to cosmic radiation in the atmosphere

International Nuclear Information System (INIS)

Beck, P.; Latocha, M.; Dorman, L.; Pelliccioni, M.; Rollet, S.

2007-01-01

As required by the European Directive 96/29/Euratom, radiation exposure due to natural ionizing radiation has to be taken into account at workplaces if the effective dose could become more than 1 mSv per year. An example of workers concerned by this directive is aircraft crew due to cosmic radiation exposure in the atmosphere. Extensive measurement campaigns on board aircraft have been carried out to assess ambient dose equivalent. A consortium of European dosimetry institutes within EURADOS WG5 summarized experimental data and results of calculations, together with detailed descriptions of the methods for measurements and calculations. The radiation protection quantity of interest is the effective dose, E (ISO). The comparison of results by measurements and calculations is done in terms of the operational quantity ambient dose equivalent, H*(10). This paper gives an overview of the EURADOS Aircraft Crew In-Flight Database and it presents a new empirical model describing fitting functions for this data. Furthermore, it describes numerical simulations performed with the Monte Carlo code FLUKA-2005 using an updated version of the cosmic radiation primary spectra. The ratio between ambient dose equivalent and effective dose at commercial flight altitudes, calculated with FLUKA-2005, is discussed. Finally, it presents the aviation dosimetry model AVIDOS based on FLUKA-2005 simulations for routine dose assessment. The code has been developed by Austrian Research Centers (ARC) for the public usage (http://avidos.healthphysics.at. (authors)

a Study of the Origin of Atmospheric Organic Aerosols

Science.gov (United States)

Hildemann, Lynn Mary

1990-01-01

The sources of ambient organic particulate matter in urban areas are investigated through a program of emission source measurements, atmospheric measurements, and mathematical modeling of source/receptor relationships. A dilution sampler intended to collect fine organic aerosol from combustion sources is designed to simulate atmospheric cooling and dilution processes, so that organic vapors which condense under ambient conditions will be collected as particulate matter. This system is used to measure the emissions from a boiler burning distillate oil, a home fireplace, catalyst and noncatalyst automobiles, heavy-duty diesel trucks, natural gas home appliances, and meat cooking operations. Alternate techniques are used to sample the particulate matter emitted from cigarette smoking, a roofing tar pot, paved road dust, brake lining wear, tire wear, and vegetative detritus. The bulk chemical characteristics of the fine aerosol fraction are presented for each source. Over half of the fine aerosol mass emitted from automobiles, wood burning, meat cooking, home appliances, cigarettes, and tar pots is shown to consist of organic compounds. The organic material collected from these sources is analyzed using high-resolution gas chromatography. Using a simple analytical protocol, a quantitative, 50-parameter characterization of the elutable fine organic aerosol emitted from each source type is obtained, which proves to be a unique fingerprint that can be used to distinguish most sources from each other. A mathematical model is used to predict the characteristics of fine ambient organic aerosol in the Los Angeles area that would prevail if the primary organic emissions are transported without chemical reaction. The model is found to track the seasonal variations observed in the ambient aerosol at the three sites studied. Emissions from vehicles and fireplaces are identified as significant sources of solvent-extractable organic aerosol. Differences between the model

Volatile organic compound (VOC) determination in working atmospheres; Determinacion de compuestos organicos volatiles (VOC) en ambiente laboral

Energy Technology Data Exchange (ETDEWEB)

Blass A, Georgina; Panama T, Luz A; Corrales C, Deyanira [Instituto de Investigaciones Electricas, Cuernavaca, Morelos (Mexico)

2003-07-01

The present work describes, in a synthesized way, the implementation and application of procedures based on the normativity related to the subject of the volatile organic compounds (Volatile Organic Compounds VOC), that allow to sample, quantify and evaluate the present contamination in the working atmosphere of a refinery due to the fugitive emissions of VOC and other substances. In accordance with the corresponding normativity, more than 189 organic compounds denominated dangerous air polluting agents (Hazardous Air Pollutants, HAP) can be found in a working atmosphere, but they are the 11 main HAP that can be found in a refinery. In the present article the work made for the sampling and quantification of 5 of the 11 dangerous polluting agents of the air: benzene, toluene, xylene, iso-octane and naphthalene. [Spanish] El presente trabajo describe, de manera sintetizada, la implementacion y aplicacion de procedimientos basados en la normatividad relacionada al tema de los compuestos organicos volatiles (Volatil Organic Compounds, VOC), que permiten muestrear, cuantificar y evaluar la contaminacion presente en el ambiente laboral de una refineria debido a las emisiones fugitivas de VOC y otras sustancias. De acuerdo con la normatividad correspondiente, mas de 189 compuestos organicos denominados contaminantes peligrosos del aire (Hazardous Air Pollutants, HAP), pueden ser encontrados en un ambiente laboral, pero son 11 los principales HAP que pueden ser hallados en una refineria. En el presente articulo se informa el trabajo realizado para el muestreo y cuantificacion de 5 de los 11 contaminantes peligrosos del aire: benceno, tolueno, xileno, iso-octano y naftaleno.

Compensation for the Effects of Ambient Conditions on the Calibration of Multi-Capillary Pressure Drop Standards

Directory of Open Access Journals (Sweden)

Colard S

2014-12-01

Full Text Available Cigarette draw resistance and filter pressure drop (PD are both major physical parameters for the tobacco industry. Therefore these parameters must be measured reliably. For these measurements, specific equipment calibrated with PD transfer standards is used. Each transfer standard must have a known and stable PD value, such standards usually being composed of several capillary tubes associated in parallel. However, PD values are modified by ambient conditions during calibration of such standards, i.e. by temperature and relative humidity (RH of air, and atmospheric pressure. In order to reduce the influence of these ambient factors, a simplified model was developed for compensating the effects of ambient conditions on the calibration of multi-capillary PD standards.

Unexpected O and O3 production in the effluent of He/O2 microplasma jets emanating into ambient air

International Nuclear Information System (INIS)

Ellerweg, D; Von Keudell, A; Benedikt, J

2012-01-01

Microplasma jets are commonly used to treat samples in ambient air. The effect of admixing air into the effluent may severely affect the composition of the emerging species. Here, the effluent of a He/O 2 microplasma jet has been analyzed in a helium and in an air atmosphere by molecular beam mass spectrometry. First, the composition of the effluent in air was recorded as a function of the distance to determine how fast air admixes into the effluent. Then, the spatial distribution of atomic oxygen and ozone in the effluent was recorded in ambient air and compared with measurements in a helium atmosphere. Additionally, a fluid model of the gas flow with reaction kinetics of reactive oxygen species in the effluent was constructed. In ambient air, the O density declines only slightly faster with distance compared with a helium atmosphere. In contrast, the O 3 density in ambient air increases significantly faster with distance compared with a helium atmosphere. This unexpected behavior cannot be explained by simple recombination reactions of O atoms with O 2 molecules. A reaction scheme involving the reaction of plasma-produced excited O 2 * species of unknown identity with ground state O 2 molecules is proposed as a possible explanation for these observations. (paper)

Methodology and significance of studies of atmospheric deposition in highway runoff

Science.gov (United States)

Colman, John A.; Rice, Karen C.; Willoughby, Timothy C.

2001-01-01

gases by impaction, especially during precipitation periods.Ultimately, traffic and road maintenance may be determined to be the source of many constituents measured in highway runoff previously attributed to ambient atmospheric deposition. An investigative design using tracers of ambient deposition that are not present in highway traffic sources could determine conclusively what fraction of highway runoff load is contributed by ambient atmospheric deposition.

Mathematical modeling of atmospheric fine particle-associated primary organic compound concentrations

Science.gov (United States)

Rogge, Wolfgang F.; Hildemann, Lynn M.; Mazurek, Monica A.; Cass, Glen R.; Simoneit, Bernd R. T.

1996-08-01

An atmospheric transport model has been used to explore the relationship between source emissions and ambient air quality for individual particle phase organic compounds present in primary aerosol source emissions. An inventory of fine particulate organic compound emissions was assembled for the Los Angeles area in the year 1982. Sources characterized included noncatalyst- and catalyst-equipped autos, diesel trucks, paved road dust, tire wear, brake lining dust, meat cooking operations, industrial oil-fired boilers, roofing tar pots, natural gas combustion in residential homes, cigarette smoke, fireplaces burning oak and pine wood, and plant leaf abrasion products. These primary fine particle source emissions were supplied to a computer-based model that simulates atmospheric transport, dispersion, and dry deposition based on the time series of hourly wind observations and mixing depths. Monthly average fine particle organic compound concentrations that would prevail if the primary organic aerosol were transported without chemical reaction were computed for more than 100 organic compounds within an 80 km × 80 km modeling area centered over Los Angeles. The monthly average compound concentrations predicted by the transport model were compared to atmospheric measurements made at monitoring sites within the study area during 1982. The predicted seasonal variation and absolute values of the concentrations of the more stable compounds are found to be in reasonable agreement with the ambient observations. While model predictions for the higher molecular weight polycyclic aromatic hydrocarbons (PAH) are in agreement with ambient observations, lower molecular weight PAH show much higher predicted than measured atmospheric concentrations in the particle phase, indicating atmospheric decay by chemical reactions or evaporation from the particle phase. The atmospheric concentrations of dicarboxylic acids and aromatic polycarboxylic acids greatly exceed the contributions that

Measurements of gaseous mercury exchanges at the sediment-water, water-atmosphere and sediment-atmosphere interfaces of a tidal environment (Arcachon Bay, France).

Science.gov (United States)

Bouchet, Sylvain; Tessier, Emmanuel; Monperrus, Mathilde; Bridou, Romain; Clavier, Jacques; Thouzeau, Gerard; Amouroux, David

2011-05-01

The elemental mercury evasion from non-impacted natural areas is of significant importance in the global Hg cycle due to their large spatial coverage. Intertidal areas represent a dynamic environment promoting the transformations of Hg species and their subsequent redistribution. A major challenge remains in providing reliable data on Hg species variability and fluxes under typical transient tidal conditions found in such environment. Field experiments were thus carried out to allow the assessment and comparison of the magnitude of the gaseous Hg fluxes at the three interfaces, sediment-water, sediment-atmosphere and water-atmosphere of a mesotidal temperate lagoon (Arcachon Bay, Aquitaine, France) over three distinct seasonal conditions. The fluxes between the sediment-water and the sediment-atmosphere interfaces were directly evaluated with field flux chambers, respectively static or dynamic. Water-atmosphere fluxes were evaluated from ambient concentrations using a gas exchange model. The fluxes at the sediment-water interface ranged from -5.0 to 5.1 ng m(-2) h(-1) and appeared mainly controlled by diffusion. The occurrence of macrophytic covers (i.e.Zostera noltii sp.) enhanced the fluxes under light radiations. The first direct measurements of sediment-atmosphere fluxes are reported here. The exchanges were more intense and variable than the two other interfaces, ranging between -78 and 40 ng m(-2) h(-1) and were mostly driven by the overlying atmospheric Hg concentrations and superficial sediment temperature. The exchanges between the water column and the atmosphere, computed as a function of wind speed and gaseous mercury saturation ranged from 0.4 to 14.5 ng m(-2) h(-1). The flux intensities recorded over the intertidal sediments periodically exposed to the atmosphere were roughly 2 to 3 times higher than the fluxes of the other interfaces. The evasion of elemental mercury from emerged intertidal sediments is probably a significant pathway for Hg evasion in

Absolute density measurements in the middle atmosphere

Directory of Open Access Journals (Sweden)

M. Rapp

2001-05-01

Full Text Available In the last ten years a total of 25 sounding rockets employing ionization gauges have been launched at high latitudes ( ~ 70° N to measure total atmospheric density and its small scale fluctuations in an altitude range between 70 and 110 km. While the determination of small scale fluctuations is unambiguous, the total density analysis has been complicated in the past by aerodynamical disturbances leading to densities inside the sensor which are enhanced compared to atmospheric values. Here, we present the results of both Monte Carlo simulations and wind tunnel measurements to quantify this aerodynamical effect. The comparison of the resulting ‘ram-factor’ profiles with empirically determined density ratios of ionization gauge measurements and falling sphere measurements provides excellent agreement. This demonstrates both the need, but also the possibility, to correct aerodynamical influences on measurements from sounding rockets. We have determined a total of 20 density profiles of the mesosphere-lower-thermosphere (MLT region. Grouping these profiles according to season, a listing of mean density profiles is included in the paper. A comparison with density profiles taken from the reference atmospheres CIRA86 and MSIS90 results in differences of up to 40%. This reflects that current reference atmospheres are a significant potential error source for the determination of mixing ratios of, for example, trace gas constituents in the MLT region.Key words. Middle atmosphere (composition and chemistry; pressure, density, and temperature; instruments and techniques

Absolute density measurements in the middle atmosphere

Directory of Open Access Journals (Sweden)

M. Rapp

Full Text Available In the last ten years a total of 25 sounding rockets employing ionization gauges have been launched at high latitudes ( ~ 70° N to measure total atmospheric density and its small scale fluctuations in an altitude range between 70 and 110 km. While the determination of small scale fluctuations is unambiguous, the total density analysis has been complicated in the past by aerodynamical disturbances leading to densities inside the sensor which are enhanced compared to atmospheric values. Here, we present the results of both Monte Carlo simulations and wind tunnel measurements to quantify this aerodynamical effect. The comparison of the resulting ‘ram-factor’ profiles with empirically determined density ratios of ionization gauge measurements and falling sphere measurements provides excellent agreement. This demonstrates both the need, but also the possibility, to correct aerodynamical influences on measurements from sounding rockets. We have determined a total of 20 density profiles of the mesosphere-lower-thermosphere (MLT region. Grouping these profiles according to season, a listing of mean density profiles is included in the paper. A comparison with density profiles taken from the reference atmospheres CIRA86 and MSIS90 results in differences of up to 40%. This reflects that current reference atmospheres are a significant potential error source for the determination of mixing ratios of, for example, trace gas constituents in the MLT region.

Key words. Middle atmosphere (composition and chemistry; pressure, density, and temperature; instruments and techniques

Onboard measurement system of atmospheric carbon monoxide in the Pacific by voluntary observing ships

Directory of Open Access Journals (Sweden)

H. Nara

2011-11-01

Full Text Available Long-term monitoring of carbon monoxide (CO mixing ratios in the atmosphere over the Pacific Ocean is being carried out on commercial cargo vessels participating in the National Institute for Environmental Studies Voluntary Observing Ships program. The program provides a regular platform for measurement of atmospheric CO along four cruise routes: from Japan to Oceania, the United States, Canada, and Southeast Asia. Flask samples are collected during every cruise for subsequent analysis in the laboratory, and in 2005, continuous shipboard CO measurements were initiated on three of the routes. Here, we describe the system we developed for onboard measurement of CO mixing ratios with a commercially available gas filter correlation CO analyzer. The fully automated system measures CO in ambient air, and the detector sensitivity and background signals are calibrated by referencing the measurements to a CO-in-air standard gas (~1 ppmv and to CO-free air scrubbed with a catalyst, respectively. We examined the artificial production of CO in the high-pressure working gas standards during storage by referencing the measurements to CO standard gases maintained as our primary scale before and after use on the ships. The onboard performance of the continuous CO measurement system was evaluated by comparing its data with data from laboratory analyses of flask samples using gas chromatography with a reduction gas detector. The reasonably good consistency between the two independent measurement methods demonstrated the good performance of both methods over the course of 3–5 years. The continuous measurement system was more useful than the flask sampling method for regionally polluted air masses, which were often encountered on Southeast Asian cruises.

Onboard measurement system of atmospheric carbon monoxide in the Pacific by voluntary observing ships

Science.gov (United States)

Nara, H.; Tanimoto, H.; Nojiri, Y.; Mukai, H.; Machida, T.; Tohjima, Y.

2011-11-01

Long-term monitoring of carbon monoxide (CO) mixing ratios in the atmosphere over the Pacific Ocean is being carried out on commercial cargo vessels participating in the National Institute for Environmental Studies Voluntary Observing Ships program. The program provides a regular platform for measurement of atmospheric CO along four cruise routes: from Japan to Oceania, the United States, Canada, and Southeast Asia. Flask samples are collected during every cruise for subsequent analysis in the laboratory, and in 2005, continuous shipboard CO measurements were initiated on three of the routes. Here, we describe the system we developed for onboard measurement of CO mixing ratios with a commercially available gas filter correlation CO analyzer. The fully automated system measures CO in ambient air, and the detector sensitivity and background signals are calibrated by referencing the measurements to a CO-in-air standard gas (~1 ppmv) and to CO-free air scrubbed with a catalyst, respectively. We examined the artificial production of CO in the high-pressure working gas standards during storage by referencing the measurements to CO standard gases maintained as our primary scale before and after use on the ships. The onboard performance of the continuous CO measurement system was evaluated by comparing its data with data from laboratory analyses of flask samples using gas chromatography with a reduction gas detector. The reasonably good consistency between the two independent measurement methods demonstrated the good performance of both methods over the course of 3-5 years. The continuous measurement system was more useful than the flask sampling method for regionally polluted air masses, which were often encountered on Southeast Asian cruises.

Effect of ambient gas density for diesel spray; Diesel funmu ni taisuru fun`iki mitsudo no eikyo

Energy Technology Data Exchange (ETDEWEB)

Yokohashi, M; Suzuki, T; Oshima, R [Tohokugakuin University, Sendai (Japan); Ono, A [Shinryo Corp., Tokyo (Japan)

1997-10-01

Effect of ambient gas density for fuel spray are measured to investigate the Diesel spray behavior. The change of ambient gas density has been given by pressuring N2 gas and using a high density atmospheric pressure SF6 gas. The measurement are performed for the spray penetration and angle. As a result, the spray penetration is confirmed same tendency at the change of density by pressuring N2 and using SF6. Though spray angle is required modification with viscosity. 2 refs., 11 figs.

Measurement of Ambient Air Motion of D. I. Gasoline Spray by LIF-PIV

Science.gov (United States)

Yamakawa, Masahisa; Isshiki, Seiji; Yoshizaki, Takuo; Nishida, Keiya

Ambient air velocity distributions in and around a D. I. gasoline spray were measured using a combination of LIF and PIV techniques. A rhodamine and water solution was injected into ambient air to disperse the fine fluorescent liquid particles used as tracers. A fuel spray was injected into the fluorescent tracer cloud and was illuminated by an Nd: YAG laser light sheet (532nm). The scattered light from the spray droplets and tracers was cut off by a high-pass filter (>560nm). As the fluorescence (>600nm) was transmitted through the high-pass filter, the tracer images were captured using a CCD camera and the ambient air velocity distribution could be obtained by PIV based on the images. This technique was applied to a D. I. gasoline spray. The ambient air flowed up around the spray and entered into the tail of the spray. Furthermore, the relative velocity between the spray and ambient air was investigated.

Development of an Automated Diffusion Scrubber-Conductometry System for Measuring Atmospheric Ammonia

International Nuclear Information System (INIS)

Lee, Bok Young; Lee, Chong Keun; Lee, Dong Soo

2011-01-01

A semi-continuous and automated method for quantifying atmospheric ammonia at the parts per billion level has been developed. The instrument consists of a high efficiency diffusion scrubber, an electrolytic on-line anion exchange device, and a conductivity detector. Water soluble gases in sampled air diffuse through the porous membrane and are absorbed in an absorbing solution. Interferences are eliminated by using an anion exchange devises. The electrical conductivity of the solution is measured without chromatographic separation. The collection efficiency was over 99%. Over the 0-200 ppbv concentration range, the calibration was linear with r"2 = 0.99. The lower limit of detection was 0.09 ppbv. A parallel analysis of Seoul air over several days using this method and a diffusion scrubber coupled to an ion chromatography system showed acceptable agreement, r"2 = 0.940 (n = 686). This method can be applied for ambient air monitoring of ammonia

Global atmospheric particle formation from CERN CLOUD measurements

CERN Document Server

Dunne, E M; Kurten, A; Almeida, J; Duplissy, J; Williamson, C; Ortega, I K; Pringle, K J; Adamov, A; Baltensperger, U; Barmet, P; Benduhn, F; Bianchi, F; Breitenlechner, M; Clarke, A; Curtius, J; Dommen, J; Donahue, N M; Ehrhart, S; Flagan, R C; Franchin, A; Guida, R; Hakala, J; Hansel, A; Heinritzi, M; Jokinen, T; Kangasluoma, J; Kirkby, J; Kulmala, M; Kupc, A; Lawler, M J; Lehtipalo, K; Makhmutov, V; Mann, G; Mathot, S; Merikanto, J; Miettinen, P; Nenes, A; Onnela, A; Rap, A; Reddington, C L S; Riccobono, F; Richards, N A D; Rissanen, M P; Rondo, L; Sarnela, N; Schobesberger, S; Sengupta, K; Simon, M; Sipila, M; Smith, J N; Stozkhov, Y; Tome, A; Trostl, J; Wagner, P E; Wimmer, D; Winkler, P M; Worsnop, D R; Carslaw, K S

2016-01-01

Fundamental questions remain about the origin of newly formed atmospheric aerosol particles because data from laboratory measurements have been insufficient to build global models. In contrast, gas-phase chemistry models have been based on laboratory kinetics measurements for decades. Here we build a global model of aerosol formation using extensive laboratory-measured nucleation rates involving sulfuric acid, ammonia, ions and organic compounds. The simulations and a comparison with atmospheric observations show that nearly all nucleation throughout the present-day atmosphere involves ammonia or biogenic organic compounds in addition to sulfuric acid. A significant fraction of nucleation involves ions, but the relatively weak dependence on ion concentrations indicates that for the processes studied variations in cosmic ray intensity do not significantly affect climate via nucleation in the present-day atmosphere.

Volatile organic compounds in urban atmospheres: Long-term measurements of ambient air concentrations in differently loaded regions of Leipzig

Energy Technology Data Exchange (ETDEWEB)

Knobloch, T.; Asperger, A.; Engewald, W. [University of Leipzig, Institute of Analytical Chemistry, Leipzig (Germany)

1997-09-01

For the comprehensive characterization of ambient air concentrations of a broad spectrum of volatile organic compounds (VOCs) an analytical method is described, consisting of adsorptive enrichment, thermal desorption without cryofocusing, and capillary gas chromatographic separation. The method was applied during two-week measuring campaigns in winter and summer 1995, and in the winter of 1996. Long-term sampling was carried out at sampling points in residential areas in the suburbs and near the city center of Leipzig. About 70 VOCs - mainly hydrocarbons from propene to hexadecane - were identified both by GC-MS and chromatographic retention data and quantified after external calibration. Mean values of VOC concentrations obtained during the sampling periods are reported and discussed with regard to the topographical location of the sampling points in the Leipzig area, seasonal variations, and possible emission sources. (orig.) With 7 figs., 3 tabs., 18 refs.

Turbine airfoil with ambient cooling system

Science.gov (United States)

Campbell, Jr, Christian X.; Marra, John J.; Marsh, Jan H.

2016-06-07

A turbine airfoil usable in a turbine engine and having at least one ambient air cooling system is disclosed. At least a portion of the cooling system may include one or more cooling channels configured to receive ambient air at about atmospheric pressure. The ambient air cooling system may have a tip static pressure to ambient pressure ratio of at least 0.5, and in at least one embodiment, may include a tip static pressure to ambient pressure ratio of between about 0.5 and about 3.0. The cooling system may also be configured such that an under root slot chamber in the root is large to minimize supply air velocity. One or more cooling channels of the ambient air cooling system may terminate at an outlet at the tip such that the outlet is aligned with inner surfaces forming the at least one cooling channel in the airfoil to facilitate high mass flow.

Water and organic nitrate detection in an AMS. Laboratory characterization and application to ambient measurements

Energy Technology Data Exchange (ETDEWEB)

Mensah, Amewu A.

2011-08-12

Atmospheric aerosols were studied by three different means. Laboratory experiments determined the relative ionization efficiency of water (RIE{sub H2O}) in an Aerodyne Aerosol Mass Spectrometers (AMS), simulation chamber experiments gave insight to the reaction products of biogenic volatile organic compounds (BVOC) oxidation products, and the findings were applied to two field campaign measurements at Cabauw, NL, in May 2008 and February 2009. Knowing the liquid water content of aerosol particles is vital for the assessment of their climate forcing potential. A value of 2 for RIE{sub H2O} was determined by studying oxalate salts with different amounts of crystal water. BVOCs contribute much more to the global budget of VOCs than anthropogenic ones but oxidation products in terms of secondary organic aerosol often correlate to anthropogenic tracers such as NO{sub x} from fossil fuel burning. In atmospheric simulation chamber experiments, organic nitrates from BVOC-NO{sub 3} oxidation showed higher vapor pressures than pure organic compounds produced in the same reactions. Organic nitrates comprised up to approx. 41 % of the particulate phase. A specific fragmentation ratio of nitrate (NO{sub 2}{sup +}/NO{sup +}) of 0.1 was found by high resolution AMS analysis differing strongly from the value of 0.4 known for the most abundant ambient NO{sub 3} specie (NH{sub 4}NO{sub 3}). Ambient average particulate mass loadings were 9.72 {mu}g/m{sup 3} dominated by organics (40 %) in 2008 and 5.62 {mu}g/m{sup 3} dominated by nitrate (42 %) in 2009. Data comparison to collocated instruments showed good agreement. Positive Matrix Factorization analysis of the particulate organic fraction distinguished semi and low volatile oxygenated organic aerosol (OOA) as well as hydrocarbon like organic aerosol (HOA) in both campaigns. An additional highly oxygenated OA with a mass spectrum very similar to fulvic acid was found in 2008. The average contribution of organic nitrate to the

Ambient RF energy scavenging: GSM and WLAN power density measurements

NARCIS (Netherlands)

Visser, H.J.; Reniers, A.C.F.; Theeuwes, J.A.C.

2009-01-01

To assess the feasibility of ambient RF energy scavenging, a survey of expected power density levels distant from GSM-900 and GSM-1800 base stations has been conducted and power density measurements have been performed in a WLAN environment. It appears that for distances ranging from 25 m to 100 m

Future of Atmospheric Neutrino Measurements

International Nuclear Information System (INIS)

Choubey, Sandhya

2013-01-01

Discovery of large θ 13 has opened up the possibility of determining the neutrino mass hierarchy and θ 23 octant through earth matter effects. The atmospheric neutrinos pick up large earth matter effects both in the ν e and ν μ channels, which if observed could lead to the determination of the mass hierarchy and θ 23 octant using this class of experiments in the near future. In this talk I review the status and prospects of future atmospheric neutrino measurements in determining the mass hierarchy and octant of θ 23

Photosynthesis and growth response of almond to increased atmospheric ozone partial pressures

International Nuclear Information System (INIS)

Retzlaff, W.A.; Williams, L.E.; DeJong, T.M.

1992-01-01

Uniform nursery stock of five almond cultivars [Prunus dulcis (Mill) D.A. Webb syn. P. amygdalus Batsch, cv. Butte, Carmel, Mission, Nonpareil, and Sonora] propagated on peach (P. domstica L. Batsch.) rootstock were exposed to three different atmospheric ozone (O 3 ) partial pressures. The trees were planted in open-top fumigation chambers on 19 Apr. 1989 at the University of California Kearny Agricultural Center located in the San Joaquin Valley of California. Exposures of the trees to three atmospheric O 3 partial pressures lasted from 1 June to 2 Nov. 1989. The mean 12-h [0800-2000 h Pacific Daylight Time (PDT)] O 3 partial pressures measured in the open-top chambers during the experimental period were 0.038, 0.060, and 0.112 μPa Pa -1 O 3 in the charcoal filtered, ambient, and ambient + O 3 treatments, respectively. Leaf net CO 2 assimilation, trunk cross-sectional area growth, and root, trunk, foliage, and total dry weight of Nonpareil were reduced by increased atmospheric O 3 partial pressures. Mission was unaffected by O 3 and Butte, Carmel, and Sonora were intermediate in their responses. Foliage of Nonpareil also abscised prematurely in the ambient and ambient + O 3 treatments. The results indicate that there are almond cultivars that are sensitive to O 3 exposure

Superconducting-Magnet-Based Faraday Rotation Spectrometer for Real Time in Situ Measurement of OH Radicals at 106 Molecule/cm3 Level in an Atmospheric Simulation Chamber.

Science.gov (United States)

Zhao, Weixiong; Fang, Bo; Lin, Xiaoxiao; Gai, Yanbo; Zhang, Weijun; Chen, Wenge; Chen, Zhiyou; Zhang, Haifeng; Chen, Weidong

2018-03-20

Atmospheric simulation chambers play vital roles in the validation of chemical mechanisms and act as a bridge between field measurements and modeling. Chambers operating at atmospheric levels of OH radicals (10 6 -10 7 molecule/cm 3 ) can significantly enhance the possibility for investigating the discrepancies between the observation and model predications. However, few chambers can directly detect chamber OH radicals at ambient levels. In this paper, we report on the first combination of a superconducting magnet with midinfrared Faraday rotation spectroscopy (FRS) for real time in situ measurement of the OH concentration in an atmospheric simulation chamber. With the use of a multipass enhanced FRS, a detection limit of 3.2 × 10 6 OH/cm 3 (2σ, 4 s) was achieved with an absorption path length of 108 m. The developed FRS system provided a unique, self-calibrated analytical instrument for in situ direct measurement of chamber OH concentration.

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

Science.gov (United States)

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

1993-01-01

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

Development of accurate dimethyl sulphide primary standard gas mixtures at low nanomole per mole levels in high-pressure aluminium cylinders for ambient measurements

Science.gov (United States)

Eon Kim, Mi; Kang, Ji Hwan; Doo Kim, Yong; Lee, Dong Soo; Lee, Sangil

2018-04-01

Dimethyl sulphide (DMS) plays an important role in atmospheric chemistry and climate change. Ambient DMS is monitored in a global network and reported at sub-nanomole per mole (nmol/mol) levels. Developing traceable, accurate DMS standards at ambient levels is essential for tracking the long-term trends and understanding the role of DMS in the atmosphere. Gravimetrically prepared gas standards in cylinders are widely used for calibrating instruments. Therefore, a stable primary standard gas mixture (PSM) is required for traceable ambient DMS measurement at remote sites. In this study, to evaluate adsorption loss on the internal surface of the gas cylinder, 6 nmol mol-1 DMS gas mixtures were prepared in three types of aluminium cylinders: a cylinder without a special coating on its internal surface (AL), an Aculife IV  +  III-treated cylinder (AC), and an Experis-treated cylinder (EX). There was little adsorption loss on the EX cylinder, whereas there was substantial adsorption loss on the other two cylinders. The EX cylinder was used to prepare 0.5, 2, 5, and 7 nmol mol-1 DMS PSMs with relative expanded uncertainties of less than 0.4%. The DMS PSMs were analytically verified and consistent within a relative expanded uncertainty of less than 1.2%. The long-term stability of the 7 nmol mol-1 DMS PSM was assessed by tracking the ratio of the DMS to the internal standard, benzene. The results showed that the DMS was stable for about seven months and it was projected to be stable for more than 60 months within a relative expanded uncertainty of 3%.

Ambient pressure photoemission spectroscopy of metal surfaces

Energy Technology Data Exchange (ETDEWEB)

Baikie, Iain D., E-mail: iain@kptechnology.ltd.uk; Grain, Angela C.; Sutherland, James; Law, Jamie

2014-12-30

Highlights: • Ambient pressure photoemission spectroscopy of metals. • Rastered photon energy scan overcomes inelastic scattering. • Relationship between photoemission threshold and contact potential difference. - Abstract: We describe a novel photoemission technique utilizing a traditional Kelvin probe as a detector of electrons/atmospheric ions ejected from metallic surfaces (Au, Ag, Cu, Fe, Ni, Ti, Zn, Al) illuminated by a deep ultra-violet (DUV) source under ambient pressure. To surmount the limitation of electron scattering in air the incident photon energy is rastered rather than applying a variable retarding electric field as is used with UPS. This arrangement can be applied in several operational modes: using the DUV source to determine the photoemission threshold (Φ) with 30–50 meV resolution and also the Kelvin probe, under dark conditions, to measure contact potential difference (CPD) between the Kelvin probe tip and the metallic sample with an accuracy of 1–3 meV. We have studied the relationship between the photoelectric threshold and CPD of metal surfaces cleaned in ambient conditions. Inclusion of a second spectroscopic visible source was used to confirm a semiconducting oxide, possibly Cu{sub 2}O, via surface photovoltage measurements with the KP. This dual detection system can be easily extended to controlled gas conditions, relative humidity control and sample heating/cooling.

Evidence for the role of organics in aerosol particle formation under atmospheric conditions

International Nuclear Information System (INIS)

Metzger, A.; Dommen, J.; Duplissy, J.; Prevot, A.S.H.; Weingartner, E.; Baltensperger, U.; Verheggen, B.; Riipinen, I.; Kulmala, M.; Spracklen, D.V.; Carslaw, K.S.

2010-01-01

New particle formation in the atmosphere is an important parameter in governing the radiative forcing of atmospheric aerosols. However, detailed nucleation mechanisms remain ambiguous, as laboratory data have so far not been successful in explaining atmospheric nucleation. We investigated the formation of new particles in a smog chamber simulating the photochemical formation of H2SO4 and organic condensable species. Nucleation occurs at H2SO4 concentrations similar to those found in the ambient atmosphere during nucleation events. The measured particle formation rates are proportional to the product of the concentrations of H2SO4 and an organic molecule. This suggests that only one H2SO4 molecule and one organic molecule are involved in the rate-limiting step of the observed nucleation process. Parameterizing this process in a global aerosol model results in substantially better agreement with ambient observations compared to control runs.

Global atmospheric particle formation from CERN CLOUD measurements.

Science.gov (United States)

Dunne, Eimear M; Gordon, Hamish; Kürten, Andreas; Almeida, João; Duplissy, Jonathan; Williamson, Christina; Ortega, Ismael K; Pringle, Kirsty J; Adamov, Alexey; Baltensperger, Urs; Barmet, Peter; Benduhn, Francois; Bianchi, Federico; Breitenlechner, Martin; Clarke, Antony; Curtius, Joachim; Dommen, Josef; Donahue, Neil M; Ehrhart, Sebastian; Flagan, Richard C; Franchin, Alessandro; Guida, Roberto; Hakala, Jani; Hansel, Armin; Heinritzi, Martin; Jokinen, Tuija; Kangasluoma, Juha; Kirkby, Jasper; Kulmala, Markku; Kupc, Agnieszka; Lawler, Michael J; Lehtipalo, Katrianne; Makhmutov, Vladimir; Mann, Graham; Mathot, Serge; Merikanto, Joonas; Miettinen, Pasi; Nenes, Athanasios; Onnela, Antti; Rap, Alexandru; Reddington, Carly L S; Riccobono, Francesco; Richards, Nigel A D; Rissanen, Matti P; Rondo, Linda; Sarnela, Nina; Schobesberger, Siegfried; Sengupta, Kamalika; Simon, Mario; Sipilä, Mikko; Smith, James N; Stozkhov, Yuri; Tomé, Antonio; Tröstl, Jasmin; Wagner, Paul E; Wimmer, Daniela; Winkler, Paul M; Worsnop, Douglas R; Carslaw, Kenneth S

2016-12-02

Fundamental questions remain about the origin of newly formed atmospheric aerosol particles because data from laboratory measurements have been insufficient to build global models. In contrast, gas-phase chemistry models have been based on laboratory kinetics measurements for decades. We built a global model of aerosol formation by using extensive laboratory measurements of rates of nucleation involving sulfuric acid, ammonia, ions, and organic compounds conducted in the CERN CLOUD (Cosmics Leaving Outdoor Droplets) chamber. The simulations and a comparison with atmospheric observations show that nearly all nucleation throughout the present-day atmosphere involves ammonia or biogenic organic compounds, in addition to sulfuric acid. A considerable fraction of nucleation involves ions, but the relatively weak dependence on ion concentrations indicates that for the processes studied, variations in cosmic ray intensity do not appreciably affect climate through nucleation in the present-day atmosphere. Copyright © 2016, American Association for the Advancement of Science.

Development of an Automated Diffusion Scrubber-Conductometry System for Measuring Atmospheric Ammonia

Energy Technology Data Exchange (ETDEWEB)

Lee, Bok Young; Lee, Chong Keun; Lee, Dong Soo [Yonsei University, Seoul (Korea, Republic of)

2011-06-15

A semi-continuous and automated method for quantifying atmospheric ammonia at the parts per billion level has been developed. The instrument consists of a high efficiency diffusion scrubber, an electrolytic on-line anion exchange device, and a conductivity detector. Water soluble gases in sampled air diffuse through the porous membrane and are absorbed in an absorbing solution. Interferences are eliminated by using an anion exchange devises. The electrical conductivity of the solution is measured without chromatographic separation. The collection efficiency was over 99%. Over the 0-200 ppbv concentration range, the calibration was linear with r{sup 2} = 0.99. The lower limit of detection was 0.09 ppbv. A parallel analysis of Seoul air over several days using this method and a diffusion scrubber coupled to an ion chromatography system showed acceptable agreement, r{sup 2} = 0.940 (n = 686). This method can be applied for ambient air monitoring of ammonia.

Radon-222 related influence on ambient gamma dose.

Science.gov (United States)

Melintescu, A; Chambers, S D; Crawford, J; Williams, A G; Zorila, B; Galeriu, D

2018-04-03

Ambient gamma dose, radon, and rainfall have been monitored in southern Bucharest, Romania, from 2010 to 2016. The seasonal cycle of background ambient gamma dose peaked between July and October (100-105 nSv h -1 ), with minimum values in February (75-80 nSv h -1 ), the time of maximum snow cover. Based on 10 m a.g.l. radon concentrations, the ambient gamma dose increased by around 1 nSv h -1 for every 5 Bq m -3 increase in radon. Radon variability attributable to diurnal changes in atmospheric mixing contributed less than 15 nSv h -1 to the overall variability in ambient gamma dose, a factor of 4 more than synoptic timescale changes in air mass fetch. By contrast, precipitation-related enhancements of the ambient gamma dose were 15-80 nSv h -1 . To facilitate routine analysis, and account in part for occasional equipment failure, an automated method for identifying precipitation spikes in the ambient gamma dose was developed. Lastly, a simple model for predicting rainfall-related enhancement of the ambient gamma dose is tested against rainfall observations from events of contrasting duration and intensity. Results are also compared with those from previously published models of simple and complex formulation. Generally, the model performed very well. When simulations underestimated observations the absolute difference was typically less than the natural variability in ambient gamma dose arising from atmospheric mixing influences. Consequently, combined use of the automated event detection method and the simple model of this study could enable the ambient gamma dose "attention limit" (which indicates a potential radiological emergency) to be reduced from 200 to 400% above background to 25-50%. Copyright © 2018 Elsevier Ltd. All rights reserved.

Propagation of atmospheric pressure helium plasma jet into ambient air at laminar gas flow

Science.gov (United States)

Pinchuk, M.; Stepanova, O.; Kurakina, N.; Spodobin, V.

2017-05-01

The formation of an atmospheric pressure plasma jet (APPJ) in a gas flow passing through the discharge gap depends on both gas-dynamic properties and electrophysical parameters of the plasma jet generator. The paper presents the results of experimental and numerical study of the propagation of the APPJ in a laminar flow of helium. A dielectric-barrier discharge (DBD) generated inside a quartz tube equipped with a coaxial electrode system, which provided gas passing through it, served as a plasma source. The transition of the laminar regime of gas flow into turbulent one was controlled by the photography of a formed plasma jet. The corresponding gas outlet velocity and Reynolds numbers were revealed experimentally and were used to simulate gas dynamics with OpenFOAM software. The data of the numerical simulation suggest that the length of plasma jet at the unvarying electrophysical parameters of DBD strongly depends on the mole fraction of ambient air in a helium flow, which is established along the direction of gas flow.

Dependence of Acetate-Based Antisolvents for High Humidity Fabrication of CH3NH3PbI3 Perovskite Devices in Ambient Atmosphere.

Science.gov (United States)

Yang, Fu; Kapil, Gaurav; Zhang, Putao; Hu, Zhaosheng; Kamarudin, Muhammad Akmal; Ma, Tingli; Hayase, Shuzi

2018-05-16

High-efficiency perovskite solar cells (PSCs) need to be fabricated in the nitrogen-filled glovebox by the atmosphere-controlled crystallization process. However, the use of the glovebox process is of great concern for mass level production of PSCs. In this work, notable efficient CH 3 NH 3 PbI 3 solar cells can be obtained in high humidity ambient atmosphere (60-70% relative humidity) by using acetate as the antisolvent, in which dependence of methyl, ethyl, propyl, and butyl acetate on the crystal growth mechanism is discussed. It is explored that acetate screens the sensitive perovskite intermediate phases from water molecules during perovskite film formation and annealing. It is revealed that relatively high vapor pressure and high water solubility of methyl acetate (MA) leads to the formation of highly dense and pinhole free perovskite films guiding to the best power conversion efficiency (PCE) of 16.3% with a reduced hysteresis. The devices prepared using MA showed remarkable shelf life stability of more than 80% for 360 h in ambient air condition, when compared to the devices fabricated using other antisolvents with low vapor pressure and low water solubility. Moreover, the PCE was still kept at 15.6% even though 2 vol % deionized water was added in the MA for preparing the perovskite layer.

Ship-Based Measurements of Atmospheric Mercury Concentrations over the Baltic Sea

Directory of Open Access Journals (Sweden)

Hanna Hoglind

2018-02-01

Full Text Available Mercury is a toxic pollutant emitted from both natural sources and through human activities. A global interest in atmospheric mercury has risen ever since the discovery of the Minamata disease in 1956. Properties of gaseous elemental mercury enable long range transport, which can cause pollution even in pristine environments. Gaseous elemental mercury (GEM was measured from winter 2016 to spring 2017 over the Baltic Sea. A Tekran 2357A mercury analyser was installed aboard the research and icebreaking vessel Oden for the purpose of continuous measurements of gaseous mercury in ambient air. Measurements were performed during a campaign along the Swedish east coast and in the Bothnian Bay near Lulea during the icebreaking season. Data was evaluated from Gothenburg using plotting software, and back trajectories for air masses were calculated. The GEM average of 1.36 ± 0.054 ng/m3 during winter and 1.29 ± 0.140 ng/m3 during spring was calculated as well as a total average of 1.36 ± 0.16 ng/m3. Back trajectories showed a possible correlation of anthropogenic sources elevating the mercury background level in some areas. There were also indications of depleted air, i.e., air with lower concentrations than average, being transported from the Arctic to northern Sweden, resulting in a drop in GEM levels.

Mass Spectrometry Imaging under Ambient Conditions

Science.gov (United States)

Wu, Chunping; Dill, Allison L.; Eberlin, Livia S.; Cooks, R. Graham; Ifa, Demian R.

2012-01-01

Mass spectrometry imaging (MSI) has emerged as an important tool in the last decade and it is beginning to show potential to provide new information in many fields owing to its unique ability to acquire molecularly specific images and to provide multiplexed information, without the need for labeling or staining. In MSI, the chemical identity of molecules present on a surface is investigated as a function of spatial distribution. In addition to now standard methods involving MSI in vacuum, recently developed ambient ionization techniques allow MSI to be performed under atmospheric pressure on untreated samples outside the mass spectrometer. Here we review recent developments and applications of MSI emphasizing the ambient ionization techniques of desorption electrospray ionization (DESI), laser ablation electrospray ionization (LAESI), probe electrospray ionization (PESI), desorption atmospheric pressure photoionization (DAPPI), femtosecond laser desorption ionization (fs-LDI), laser electrospray mass spectrometry (LEMS), infrared laser ablation metastable-induced chemical ionization (IR-LAMICI), liquid microjunction surface sampling probe mass spectrometry (LMJ-SSP MS), nanospray desorption electrospray ionization (nano-DESI), and plasma sources such as the low temperature plasma (LTP) probe and laser ablation coupled to flowing atmospheric-pressure afterglow (LA-FAPA). Included are discussions of some of the features of ambient MSI including the ability to implement chemical reactions with the goal of providing high abundance ions characteristic of specific compounds of interest and the use of tandem mass spectrometry to either map the distribution of targeted molecules with high specificity or to provide additional MS information in the structural identification of compounds. We also describe the role of bioinformatics in acquiring and interpreting the chemical and spatial information obtained through MSI, especially in biological applications for tissue

Volatility measurement of atmospheric submicron aerosols in an urban atmosphere in southern China

Directory of Open Access Journals (Sweden)

L.-M. Cao

2018-02-01

Full Text Available Aerosol pollution has been a very serious environmental problem in China for many years. The volatility of aerosols can affect the distribution of compounds in the gas and aerosol phases, the atmospheric fates of the corresponding components, and the measurement of the concentration of aerosols. Compared to the characterization of chemical composition, few studies have focused on the volatility of aerosols in China. In this study, a thermodenuder aerosol mass spectrometer (TD-AMS system was deployed to study the volatility of non-refractory submicron particulate matter (PM1 species during winter in Shenzhen. To our knowledge, this paper is the first report of the volatilities of aerosol chemical components based on a TD-AMS system in China. The average PM1 mass concentration during the experiment was 42.7±20.1 µg m−3, with organic aerosol (OA being the most abundant component (43.2 % of the total mass. The volatility of chemical species measured by the AMS varied, with nitrate showing the highest volatility, with a mass fraction remaining (MFR of 0.57 at 50 °C. Organics showed semi-volatile characteristics (the MFR was 0.88 at 50 °C, and the volatility had a relatively linear correlation with the TD temperature (from the ambient temperature to 200 °C, with an evaporation rate of 0.45 % °C−1. Five subtypes of OA were resolved from total OA using positive matrix factorization (PMF for data obtained under both ambient temperature and high temperatures through the TD, including a hydrocarbon-like OA (HOA, accounting for 13.5 %, a cooking OA (COA, 20.6 %, a biomass-burning OA (BBOA, 8.9 %, and two oxygenated OAs (OOAs: a less-oxidized OOA (LO-OOA, 39.1 % and a more-oxidized OOA (MO-OOA, 17.9 %. Different OA factors presented different volatilities, and the volatility sequence of the OA factors at 50 °C was HOA (MFR of 0.56  >  LO-OOA (0.70  >  COA (0.85  ≈  BBOA (0.87�

EPR-based distance measurements at ambient temperature.

Science.gov (United States)

Krumkacheva, Olesya; Bagryanskaya, Elena

2017-07-01

Pulsed dipolar (PD) EPR spectroscopy is a powerful technique allowing for distance measurements between spin labels in the range of 2.5-10.0nm. It was proposed more than 30years ago, and nowadays is widely used in biophysics and materials science. Until recently, PD EPR experiments were limited to cryogenic temperatures (TEPR as well as other approaches based on EPR (e.g., relaxation enhancement; RE). In this paper, we review the features of PD EPR and RE at ambient temperatures, in particular, requirements on electron spin phase memory time, ways of immobilization of biomolecules, the influence of a linker between the spin probe and biomolecule, and future opportunities. Copyright © 2017 Elsevier Inc. All rights reserved.

Onboard measurement system of atmospheric carbon monoxide over the Pacific Ocean by voluntary observing ships

Science.gov (United States)

Nara, H.; Tanimoto, H.; Nojiri, Y.; Mukai, H.; Machida, T.; Tohjima, Y.

2011-07-01

Long-term monitoring of carbon monoxide (CO) mixing ratios in the atmosphere over the Pacific Ocean is being carried out on commercial cargo vessels participating in the National Institute for Environmental Studies Voluntary Observing Ships program. The program provides a regular platform for measurement of atmospheric CO along four cruising routes: from Japan to Oceania, from Japan to the United States, from Japan to Canada, and from Japan to Southeast Asia. Flask samples are collected during every cruise for subsequent analysis in the laboratory, and in 2005, continuous shipboard CO measurements were initiated on three of the routes. Here, we describe the system we developed for onboard measurement of CO mixing ratios with a commercially available gas filter correlation CO analyzer. The fully automated system measures CO in ambient air, and the detector sensitivity and background signals are calibrated by referencing the measurements to a CO-in-air standard gas (~1 ppmv) and to CO-free air scrubbed with a catalyst, respectively. We examined the artificial production of CO in the high-pressure working gas standards (CO balanced with purified air at ppmv levels) during storage by referencing the measurements to CO standard gases maintained as our primary scale before and after use on the ships. The onboard performance of the continuous CO measurement system was evaluated by comparing its data with data from laboratory analyses of flask samples using gas chromatography with a reduction gas detector. The reasonably good consistency between the two independent measurement methods demonstrated the good performance of both methods over the course of 3-5 yr. The continuous measurement system was more useful than the flask sampling method for regionally polluted air masses, which were often encountered on Southeast Asian cruises.

On the Application of Hall Thruster Working with Ambient Atmospheric Gas for Orbital Station-Keeping

Directory of Open Access Journals (Sweden)

D. V. Duhopel'nikov

2016-01-01

Full Text Available The paper considers the application of the Hall thruster using the ambient atmospheric air for orbital station keeping. This is a relevant direction at the up-to-date development stage of propulsion systems. Many teams of designers of electric rocket thrusters evaluate the application of different schemes of particle acceleration at the low-earth orbit. Such technical solution allows us to abandon the storage systems of the working agent on the spacecraft board. Thus, lifetime of such a system at the orbit wouldn`t be limited by fuel range. The paper suggests a scheme of the propulsion device with a parabolic confuser that provides a required compression ratio of the ambient air for correct operation. Formulates physical and structural restrictions on ambient air to be used as a working agent of the thruster. Pointes out that the altitudes from 200 to 300 km are the most promising for such propulsion devices. Shows that for operation at lower altitudes are required the higher capacities that are not provided by modern onboard power supply systems. For the orbit heightening the air intakes with significant compression rate are of necessity. The size of such air intakes would exceed nose fairing of exploited space launch systems. To perform further design calculations are shown dependencies that allow us to calculate an effective diameter of the thruster channel and a critical voltage to be desirable for thrust force excess over air resistance. The dependencies to calculate minimal and maximal fluxes of neutral particles of oxygen and nitrogen, that are necessary for normal thruster operation, are also shown. Calculation results of the propulsion system parameters for the spacecrafts with cross-sectional area within 1 - 3 m2 and inlet diameter of air intake within 1 - 3 m are demonstrated. The research results have practical significance in design of advanced propulsion devices for lowaltitude spacecrafts. The work has been supported by the RFFR

Atmospheric radiation measurement program facilities newsletter, June 2002.; TOPICAL

International Nuclear Information System (INIS)

Holdridge, D. J.

2002-01-01

ARM Intensive Operational Period Scheduled to Validate New NASA Satellite-Beginning in July, all three ARM sites (Southern Great Plains[SGP], North Slope of Alaska, and Tropical Western Pacific; Figure 1) will participate in the AIRS Validation IOP. This three-month intensive operational period (IOP) will validate data collected by the satellite-based Atmospheric Infrared Sounder (AIRS) recently launched into space. On May 4, the National Aeronautics and Space Administration (NASA) launched Aqua, the second spacecraft in the Earth Observing System (EOS) series. The EOS satellites monitor Earth systems including land surfaces, oceans, the atmosphere, and ice cover. The first EOS satellite, named Terra, was launched in December 1999. The second EOS satellite is named Aqua because its primary focus is understanding Earth's water cycle through observation of atmospheric moisture, clouds, temperature, ocean surface, precipitation, and soil moisture. One of the instruments aboard Aqua is the AIRS, built by the Jet Propulsion Laboratory, a NASA agency. The AIRS Validation IOP complements the ARM mission to improve understanding of the interactions of clouds and atmospheric moisture with solar radiation and their influence on weather and climate. In support of satellite validation IOP, ARM will launch dedicated radiosondes at all three ARM sites while the Aqua satellite with the AIRS instrument is orbiting overhead. These radiosonde launches will occur 45 minutes and 5 minutes before selected satellite overpasses. In addition, visiting scientists from the Jet Propulsion Laboratory will launch special radiosondes to measure ozone and humidity over the SGP site. All launches will generate ground-truth data to validate satellite data collected simultaneously. Data gathered daily by ARM meteorological and solar radiation instruments will complete the validation data sets. Data from Aqua-based instruments, including AIRS, will aid in weather forecasting, climate modeling, and

Influence of oil and gas emissions on ambient atmospheric non-methane hydrocarbons in residential areas of Northeastern Colorado

Directory of Open Access Journals (Sweden)

Chelsea R. Thompson

2014-11-01

Full Text Available Abstract The Northern Front Range (NFR region of Colorado has experienced rapid expansion of oil and gas extraction from shale and tight sands reservoirs in recent years due to advances in hydraulic fracturing technology, with over 25,000 wells currently in operation. This region has also been designated as a federal ozone non-attainment area by the U.S. EPA. High ozone levels are a significant health concern, as are potential health impacts from chronic exposure to primary emissions of non-methane hydrocarbons (NMHC for residents living near wells. From measurements of ambient atmospheric NMHC present in residential areas located in close proximity to wells in Erie, Colorado, we find that mean mole fractions of the C2–C5 alkanes are enhanced by a factor of 18–77 relative to the regional background, and present at higher levels than typically found in large urban centers. When combined with NMHC observations from downtown Denver and Platteville, it is apparent that these compounds are elevated across the NFR, with highest levels within the Greater Wattenberg Gas Field. This represents a large area source for ozone precursors in the NFR. The BTEX aromatic compounds in Erie were comparable to (e.g., benzene or lower than (e.g., toluene, ethylbenzene, xylene in large urban centers, however, benzene was significantly higher in Platteville, and within the range of chronic health-based exposure levels. An initial look at comparisons with data sets from previous years reveal that ambient levels for oil and gas-related NMHC in Erie, as well as further downwind in Boulder, have not decreased, but appear to have been increasing, despite tightening of emissions standards for the oil and gas industries in 2008.

Cavity ring-down spectroscopy (CRDS) system for measuring atmospheric mercury using differential absorption

Science.gov (United States)

Pierce, A.; Obrist, D.; Moosmuller, H.; Moore, C.

2012-04-01

Atmospheric elemental mercury (Hg0) is a globally pervasive element that can be transported and deposited to remote ecosystems where it poses — particularly in its methylated form — harm to many organisms including humans. Current techniques for measurement of atmospheric Hg0 require several liters of sample air and several minutes for each analysis. Fast-response (i.e., 1 second or faster) measurements would improve our ability to understand and track chemical cycling of mercury in the atmosphere, including high frequency Hg0 fluctuations, sources and sinks, and chemical transformation processes. We present theory, design, challenges, and current results of our new prototype sensor based on cavity ring-down spectroscopy (CRDS) for fast-response measurement of Hg0 mass concentrations. CRDS is a direct absorption technique that implements path-lengths of multiple kilometers in a compact absorption cell using high-reflectivity mirrors, thereby improving sensitivity and reducing sample volume compared to conventional absorption spectroscopy. Our sensor includes a frequency-doubled, dye-laser emitting laser pulses tunable from 215 to 280 nm, pumped by a Q-switched, frequency tripled Nd:YAG laser with a pulse repetition rate of 50 Hz. We present how we successfully perform automated wavelength locking and stabilization of the laser to the peak Hg0 absorption line at 253.65 nm using an external isotopically-enriched mercury (202Hg0) cell. An emphasis of this presentation will be on the implementation of differential absorption measurement whereby measurements are alternated between the peak Hg0 absorption wavelength and a nearby wavelength "off" the absorption line. This can be achieved using a piezo electric tuning element that allows for pulse-by-pulse tuning and detuning of the laser "online" and "offline" of the Hg absorption line, and thereby allows for continuous correction of baseline extinction losses. Unexpected challenges with this approach included

Photosynthesis and growth response of almond to increased atmospheric ozone partial pressures

Energy Technology Data Exchange (ETDEWEB)

Retzlaff, W.A.; Williams, L.E. (Univ. of California, Davis (United States) Kearney Agricultural Center, Parlier, CA (United States)); DeJong, T.M. (Univ. of California, Davis (United States))

Uniform nursery stock of five almond cultivars [Prunus dulcis (Mill) D.A. Webb syn. P. amygdalus Batsch, cv. Butte, Carmel, Mission, Nonpareil, and Sonora] propagated on peach (P. domstica L. Batsch.) rootstock were exposed to three different atmospheric ozone (O[sub 3]) partial pressures. The trees were planted in open-top fumigation chambers on 19 Apr. 1989 at the University of California Kearny Agricultural Center located in the San Joaquin Valley of California. Exposures of the trees to three atmospheric O[sub 3] partial pressures lasted from 1 June to 2 Nov. 1989. The mean 12-h [0800-2000 h Pacific Daylight Time (PDT)] O[sub 3] partial pressures measured in the open-top chambers during the experimental period were 0.038, 0.060, and 0.112 [mu]Pa Pa[sup [minus]1] O[sub 3] in the charcoal filtered, ambient, and ambient + O[sub 3] treatments, respectively. Leaf net CO[sub 2] assimilation, trunk cross-sectional area growth, and root, trunk, foliage, and total dry weight of Nonpareil were reduced by increased atmospheric O[sub 3] partial pressures. Mission was unaffected by O[sub 3] and Butte, Carmel, and Sonora were intermediate in their responses. Foliage of Nonpareil also abscised prematurely in the ambient and ambient + O[sub 3] treatments. The results indicate that there are almond cultivars that are sensitive to O[sub 3] exposure.

Point source attribution of ambient contamination events near unconventional oil and gas development.

Science.gov (United States)

Hildenbrand, Zacariah L; Mach, Phillip M; McBride, Ethan M; Dorreyatim, M Navid; Taylor, Josh T; Carlton, Doug D; Meik, Jesse M; Fontenot, Brian E; Wright, Kenneth C; Schug, Kevin A; Verbeck, Guido F

2016-12-15

We present an analysis of ambient benzene, toluene, and xylene isomers in the Eagle Ford shale region of southern Texas. In situ air quality measurements using membrane inlet mobile mass spectrometry revealed ambient benzene and toluene concentrations as high as 1000 and 5000 parts-per-billion, respectively, originating from specific sub-processes on unconventional oil and gas well pad sites. The detection of highly variant contamination events attributable to natural gas flaring units, condensate tanks, compressor units, and hydrogen sulfide scavengers indicates that mechanical inefficiencies, and not necessarily the inherent nature of the extraction process as a whole, result in the release of these compounds into the environment. This awareness of ongoing contamination events contributes to an enhanced knowledge of ambient volatile organic compounds on a regional scale. While these reconnaissance measurements on their own do not fully characterize the fluctuations of ambient BTEX concentrations that likely exist in the atmosphere of the Eagle Ford Shale region, they do suggest that contamination events from unconventional oil and gas development can be monitored, controlled, and reduced. Copyright © 2016 Elsevier B.V. All rights reserved.

Measurements of atmospheric mercury with high time resolution: recent applications in environmental research and monitoring.

Science.gov (United States)

Ebinghaus, R; Kock, H H; Schmolke, S R

2001-11-01

In the past five years automated high time-resolution measurements of mercury species in ambient air have promoted remarkable progress in the understanding of the spatial distribution, short-term variability, and fate of this priority pollutant in the lower troposphere. Examples show the wide range of possible applications of these techniques in environmental research and monitoring. Presented applications of measurement methods for total gaseous mercury (TGM) include long-term monitoring of atmospheric mercury at a coastal station, simultaneous measurements during a south-to-north transect measurement campaign covering a distance of approximately 800 km, the operation on board of a research aircraft, and the quantification of mercury emissions from naturally enriched surface soils. First results obtained with a new method for the determination of reactive gaseous mercury (RGM) are presented. Typical background concentrations of TGM are between 1.5 and 2 ng m(-3) in the lower troposphere. Concentrations of RGM have been determined at a rural site in Germany between 2 and 35 pg m(-3). Flux measurements over naturally enriched surface soils in the Western U.S.A. have revealed emission fluxes of up to 200 ng Hg m(-1) h(-1) under dry conditions.

Ambient Sensors

NARCIS (Netherlands)

Börner, Dirk; Specht, Marcus

2014-01-01

This software sketches comprise two custom-built ambient sensors, i.e. a noise and a movement sensor. Both sensors measure an ambient value and process the values to a color gradient (green > yellow > red). The sensors were built using the Processing 1.5.1 development environment. Available under

Measurement of Ambient Air Particle (TSP, PM10, PM2,5) Around Candidate Location of PLTN Semenanjung Lemahabang

International Nuclear Information System (INIS)

AgusGindo S; Budi Hari H

2008-01-01

Measurement analysis of ambient air particle (TSP, PM 10 , PM 2,5 ) around location candidate of PLTN (Power Station of Nuclear Energy) Semenanjung Lemahabang has been carried out. The measurement was conducted in May 2007 with a purpose to providing information about concentration of ambient air particle (TSP, PM 10 , PM 2,5 ) and diameter distribution of its air particle. The measurement was conducted in three locations i.e. 1). Balong village 2). Bayuran 3). Bondo. Concentration of TSP, PM 10 , and PM 2,5 per 24 hours in all measured locations in area candidate of PLTN exceed quality standard of national ambient air is specified by government. All measurement locations for the TSP, PM 10 , and PM 2,5 was include category of ISPU (Standard Index of Air Pollution) moderate. (author)

Inter-comparison of laser photoacoustic spectroscopy and gas chromatography techniques for measurements of ethene in the atmosphere.

Science.gov (United States)

Kuster, William C; Harren, Frans J M; de Gouw, Joost A

2005-06-15

Laser photoacoustic spectroscopy (LPAS) is highly suitable for the detection of ethene in air due to the overlap between its strongest absorption lines and the wavelengths accessible by high-powered CO2 lasers. Here, we test the ability of LPAS to measure ethene in ambient air by comparing the measurements in urban air with those from a gas chromatography flame-ionization detection (GC-FID) instrument. Over the course of several days, we obtained quantitative agreement between the two measurements. Over this period, the LPAS instrument had a positive offset of 330 +/- 140 pptv (parts-per-trillion by volume) relative to the GC-FID instrument, possibly caused by interference from other species. The detection limit of the LPAS instrument is currently estimated around 1 ppbv and is limited by this offset and the statistical noise in the data. We conclude that LPAS has the potential to provide fast-response measurements of ethene in the atmosphere, with significant advantages over existing techniques when measuring from moving platforms and in the vicinity of emission sources.

The Effects of Ambient Conditions on Helicopter Harmonic Noise Radiation: Theory and Experiment

Science.gov (United States)

Greenwood, Eric; Sim, Ben W.; Boyd, D. Douglas, Jr.

2016-01-01

The effects of ambient atmospheric conditions, air temperature and density, on rotor harmonic noise radiation are characterized using theoretical models and experimental measurements of helicopter noise collected at three different test sites at elevations ranging from sea level to 7000 ft above sea level. Significant changes in the thickness, loading, and blade-vortex interaction noise levels and radiation directions are observed across the different test sites for an AS350 helicopter flying at the same indicated airspeed and gross weight. However, the radiated noise is shown to scale with ambient pressure when the flight condition of the helicopter is defined in nondimensional terms. Although the effective tip Mach number is identified as the primary governing parameter for thickness noise, the nondimensional weight coefficient also impacts lower harmonic loading noise levels, which contribute strongly to low frequency harmonic noise radiation both in and out of the plane of the horizon. Strategies for maintaining the same nondimensional rotor operating condition under different ambient conditions are developed using an analytical model of single main rotor helicopter trim and confirmed using a CAMRAD II model of the AS350 helicopter. The ability of the Fundamental Rotorcraft Acoustics Modeling from Experiments (FRAME) technique to generalize noise measurements made under one set of ambient conditions to make accurate noise predictions under other ambient conditions is also validated.

Precision Photometric Extinction Corrections from Direct Atmospheric Measurements

Science.gov (United States)

McGraw, John T.; Zimmer, P.; Linford, J.; Simon, T.; Measurement Astrophysics Research Group

2009-01-01

For decades astronomical extinction corrections have been accomplished using nightly mean extinction coefficients derived from Langley plots measured with the same telescope used for photometry. Because this technique results in lost time on program fields, observers only grudgingly made sporadic extinction measurements. Occasionally extinction corrections are not measured nightly but are made using tabulated mean monthly or even quarterly extinction coefficients. Any observer of the sky knows that Earth's atmosphere is an ever-changing fluid in which is embedded extinction sources ranging from Rayleigh (molecular) scattering to aerosol, smoke and dust scattering and absorption, to "just plain cloudy.” Our eyes also tell us that the type, direction and degree of extinction changes on time scales of minutes or less - typically shorter than many astronomical observations. Thus, we should expect that atmospheric extinction can change significantly during a single observation. Mean extinction coefficients might be well-defined nightly means, but those means have high variance because they do not accurately record the wavelength-, time-, and angle-dependent extinction actually affecting each observation. Our research group is implementing lidar measurements made in the direction of observation with one minute cadence, from which the absolute monochromatic extinction can be measured. Simultaneous spectrophotometry of nearby bright standard stars allows derivation and MODTRAN modeling atmospheric transmission as a function of wavelength for the atmosphere through which an observation is made. Application of this technique is demonstrated. Accurate real-time extinction measurements are an enabling factor for sub-1% photometry. This research is supported by NSF Grant 0421087 and AFRL Grant #FA9451-04-2-0355.

Propagation of atmospheric pressure helium plasma jet into ambient air at laminar gas flow

International Nuclear Information System (INIS)

Pinchuk, M; Kurakina, N; Spodobin, V; Stepanova, O

2017-01-01

The formation of an atmospheric pressure plasma jet (APPJ) in a gas flow passing through the discharge gap depends on both gas-dynamic properties and electrophysical parameters of the plasma jet generator. The paper presents the results of experimental and numerical study of the propagation of the APPJ in a laminar flow of helium. A dielectric-barrier discharge (DBD) generated inside a quartz tube equipped with a coaxial electrode system, which provided gas passing through it, served as a plasma source. The transition of the laminar regime of gas flow into turbulent one was controlled by the photography of a formed plasma jet. The corresponding gas outlet velocity and Reynolds numbers were revealed experimentally and were used to simulate gas dynamics with OpenFOAM software. The data of the numerical simulation suggest that the length of plasma jet at the unvarying electrophysical parameters of DBD strongly depends on the mole fraction of ambient air in a helium flow, which is established along the direction of gas flow. (paper)

Influence of ambient meteorology on the accuracy of radiation measurements: insights from field and laboratory experiments

Science.gov (United States)

Oswald, Sandro M.; Pietsch, Helga; Baumgartner, Dietmar J.; Rieder, Harald E.

2016-04-01

that precipitation (as simulated by spray-tests or observed under ambient conditions) significantly affects the thermal environment of the instruments and thus their stability. Statistical analyses during nighttime conditions showed that precipitation triggers zero offsets of 4 W/m2 or more, depending on the HV-system and prevailing ambient conditions (i.e., air temperature, wind), indicating a clear exceedance of BSRN targets. References: McArthur L. J. B.: World Climate Research Programme-Baseline Surface Radiation Network (BSRN) - Operations Manual Version 2.1, Experimental Studies Division, Atmospheric Environment Service, Downsview, Ontario, Canada, 2005. Olefs M., Baumgartner D. J., Obleitner F., Bichler C., Foelsche U., Pietsch H., Rieder H. E., Weihs P., Geyer F., Haiden T., Schöner W.: The Austrian radiation monitoring network ARAD - best practice and added value, Atmospheric Measurement Techniques Discussions, 8: 10663-10710, 2015. Ohmura A., Dutton E. G., Forgan B., Frohlich C., Gilgen H., Hegner H., Heimo A., Stephens G. L., König-Langlo G., McArthur B., Müller G., Philipona R., Pinker R., Whitlock C. H., Dehne K., Wild M.: Baseline surface radiation network (bsrn/wcrp): new precision radiometry for climate research, Bulletin of the American Meteorological Society, 79(10): 2115-2136, 1998.

Concentrations and fate of decamethylcyclopentasiloxane (D(5)) in the atmosphere.

Science.gov (United States)

McLachlan, Michael S; Kierkegaard, Amelie; Hansen, Kaj M; van Egmond, Roger; Christensen, Jesper H; Skjøth, Carsten A

2010-07-15

Decamethylcyclopentasiloxane (D(5)) is a volatile compound used in personal care products that is released to the atmosphere in large quantities. Although D(5) is currently under consideration for regulation, there have been no field investigations of its atmospheric fate. We employed a recently developed, quality assured method to measure D(5) concentration in ambient air at a rural site in Sweden. The samples were collected with daily resolution between January and June 2009. The D(5) concentration ranged from 0.3 to 9 ng m(-3), which is 1-3 orders of magnitude lower than previous reports. The measured data were compared with D(5) concentrations predicted using an atmospheric circulation model that included both OH radical and D(5) chemistry. The model was parametrized using emissions estimates and physical chemical properties determined in laboratory experiments. There was good agreement between the measured and modeled D(5) concentrations. The results show that D(5) is clearly subject to long-range atmospheric transport, but that it is also effectively removed from the atmosphere via phototransformation. Atmospheric deposition has little influence on the atmospheric fate. The good agreement between the model predictions and the field observations indicates that there is a good understanding of the major factors governing D(5) concentrations in the atmosphere.

A method of atmospheric density measurements during Shuttle entry using UV laser Rayleigh scattering

Science.gov (United States)

Mckenzie, Robert L.

1987-01-01

A detailed study is described of the performance capabilities and the hardware requirements for a method in which ambient density is measured along the Space Shuttle flight path using on-board optical instrumentation. The technique relies on Rayleigh scattering of light from a pulsed, ultraviolet, ArF excimer laser operating at a wavelength of 193 nm. The method is shown to be capable of providing direct measurements of ambient density with an uncertainty of less than 1 percent and with a spatial resolution of 1 km, over an altitude range from 50 to 90 km. In addition, extensions of this concept are discussed that allow measurements of the shock wave location and the density profile within the shock layer. Two approaches are identified that appear to be feasible, in which the same laser system is used for the extended measurements as that required for the ambient density measurements.

Blow-out limits of nonpremixed turbulent jet flames in a cross flow at atmospheric and sub-atmospheric pressures

KAUST Repository

Wang, Qiang; Hu, Longhua; Yoon, Sung Hwan; Lu, Shouxiang; Delichatsios, Michael; Chung, Suk-Ho

2015-01-01

The blow-out limits of nonpremixed turbulent jet flames in cross flows were studied, especially concerning the effect of ambient pressure, by conducting experiments at atmospheric and sub-atmospheric pressures. The combined effects of air flow

Using magnetic and chemical measurements to detect atmospherically-derived metal pollution in artificial soils and metal uptake in plants

International Nuclear Information System (INIS)

Sapkota, B.; Cioppa, M.T.

2012-01-01

Quantification of potential effects of ambient atmospheric pollution on magnetic and chemical properties of soils and plants requires precise experimental studies. A controlled growth experiment assessing magnetic and chemical parameters was conducted within (controls) and outside (exposed) a greenhouse setting. Magnetic susceptibility (MS) measurements showed that while initial MS values were similar for the sample sets, the overall MS value of exposed soil was significantly greater than in controls, suggesting an additional input of Fe-containing particles. Scanning electron microscope images of the exposed soils revealed numerous angular magnetic particles and magnetic spherules typical of vehicular exhaust and combustion processes, respectively. Similarly, chemical analysis of plant roots showed that plants grown in the exposed soil had higher concentrations of Fe and heavy (toxic) metals than controls. This evidence suggests that atmospheric deposition contributed to the MS increase in exposed soils and increased metal uptake by plants grown in this soil. - Highlights: ► Magnetic susceptibility (MS) values increased in exposed soils during the growth. ► MS values in control soils decreased from their initial values during the growth. ► Decrease in MS values due to downwards migration of Fe particles, magnetic mineral transformations and Fe uptake by plants. ► Higher metal uptake in plants grown in exposed soils than those grown in controls. ► Atmospheric particulate deposition isolated as main contributor to these effects. - Variations in atmospheric particulate levels are measurable using magnetic and chemical techniques on soils and plant biomass, and suggest pollutant levels may be higher than previously recognized.

Total Peroxy Nitrates (ΣPNs in the atmosphere: the Thermal Dissociation-Laser Induced Fluorescence (TD-LIF technique and comparisons to speciated PAN measurements

Directory of Open Access Journals (Sweden)

B. W. LaFranchi

2010-05-01

Full Text Available Peroxyacetyl nitrate (PAN and its chemical analogues are increasingly being quantified in the ambient atmosphere by thermal dissociation (TD followed by detection of either the peroxyacyl radical or the NO2 product. Here we present details of the technique developed at University of California, Berkeley which detects the sum of all peroxynitrates (ΣPNs via laser-induced fluorescence (LIF of the NO2 product. We review the various deployments and compare the Berkeley ΣPNs measurements with the sums of PAN and its homologue species detected individually by other instruments. The observed TD-LIF ΣPNs usually agree to within 10% with the summed individual species, thus arguing against the presence of significant concentrations of unmeasured PAN-type compounds in the atmosphere, as suggested by some photochemical mechanisms. Examples of poorer agreement are attributed to a sampling inlet design that is shown to be inappropriate for high NOx conditions. Interferences to the TD-LIF measurements are described along with strategies to minimize their effects.

Sampling and analyte enrichment strategies for ambient mass spectrometry.

Science.gov (United States)

Li, Xianjiang; Ma, Wen; Li, Hongmei; Ai, Wanpeng; Bai, Yu; Liu, Huwei

2018-01-01

Ambient mass spectrometry provides great convenience for fast screening, and has showed promising potential in analytical chemistry. However, its relatively low sensitivity seriously restricts its practical utility in trace compound analysis. In this review, we summarize the sampling and analyte enrichment strategies coupled with nine modes of representative ambient mass spectrometry (desorption electrospray ionization, paper vhspray ionization, wooden-tip spray ionization, probe electrospray ionization, coated blade spray ionization, direct analysis in real time, desorption corona beam ionization, dielectric barrier discharge ionization, and atmospheric-pressure solids analysis probe) that have dramatically increased the detection sensitivity. We believe that these advances will promote routine use of ambient mass spectrometry. Graphical abstract Scheme of sampling stretagies for ambient mass spectrometry.

Development and Application of an Oxidation Flow Reactor to Study Secondary Organic Aerosol Formation from Ambient Air

Science.gov (United States)

Palm, Brett Brian

Secondary organic aerosols (SOA) in the atmosphere play an important role in air quality, human health, and climate. However, the sources, formation pathways, and fate of SOA are poorly constrained. In this dissertation, I present development and application of the oxidation flow reactor (OFR) technique for studying SOA formation from OH, O3, and NO3 oxidation of ambient air. With a several-minute residence time and a portable design with no inlet, OFRs are particularly well-suited for this purpose. I first introduce the OFR concept, and discuss several advances I have made in performing and interpreting OFR experiments. This includes estimating oxidant exposures, modeling the fate of low-volatility gases in the OFR (wall loss, condensation, and oxidation), and comparing SOA yields of single precursors in the OFR with yields measured in environmental chambers. When these experimental details are carefully considered, SOA formation in an OFR can be more reliably compared with ambient SOA formation processes. I then present an overview of what OFR measurements have taught us about SOA formation in the atmosphere. I provide a comparison of SOA formation from OH, O3, and NO3 oxidation of ambient air in a wide variety of environments, from rural forests to urban air. In a rural forest, the SOA formation correlated with biogenic precursors (e.g., monoterpenes). In urban air, it correlated instead with reactive anthropogenic tracers (e.g., trimethylbenzene). In mixed-source regions, the SOA formation did not correlate well with any single precursor, but could be predicted by multilinear regression from several precursors. Despite these correlations, the concentrations of speciated ambient VOCs could only explain approximately 10-50% of the total SOA formed from OH oxidation. In contrast, ambient VOCs could explain all of the SOA formation observed from O3 and NO3 oxidation. Evidence suggests that lower-volatility gases (semivolatile and intermediate-volatility organic

Ambient ionization mass spectrometry: A tutorial

Energy Technology Data Exchange (ETDEWEB)

Huang, Min-Zong; Cheng, Sy-Chi; Cho, Yi-Tzu [Department of Chemistry, National Sun Yat-Sen University, Kaohsiung, Taiwan (China); Shiea, Jentaie, E-mail: jetea@fac.nsysu.edu.tw [Department of Chemistry, National Sun Yat-Sen University, Kaohsiung, Taiwan (China); Cancer Center, Kaohsiung Medical University, Kaohsiung, Taiwan (China)

2011-09-19

Highlights: {yields} Ambient ionization technique allows the direct analysis of sample surfaces with little or no sample pretreatment. {yields} We sort ambient ionization techniques into three main analytical strategies, direct ionization, direct desorption/ionization, and two-step ionization. {yields} The underlying principles of operation, ionization processes, detecting mass ranges, sensitivity, and representative applications of these techniques are described and compared. - Abstract: Ambient ionization is a set of mass spectrometric ionization techniques performed under ambient conditions that allows the direct analysis of sample surfaces with little or no sample pretreatment. Using combinations of different types of sample introduction systems and ionization methods, several novel techniques have been developed over the last few years with many applications (e.g., food safety screening; detection of pharmaceuticals and drug abuse; monitoring of environmental pollutants; detection of explosives for antiterrorism and forensics; characterization of biological compounds for proteomics and metabolomics; molecular imaging analysis; and monitoring chemical and biochemical reactions). Electrospray ionization and atmospheric pressure chemical ionization are the two main ionization principles most commonly used in ambient ionization mass spectrometry. This tutorial paper provides a review of the publications related to ambient ionization techniques. We describe and compare the underlying principles of operation, ionization processes, detecting mass ranges, sensitivity, and representative applications of these techniques.

Ambient ionization mass spectrometry: A tutorial

International Nuclear Information System (INIS)

Huang, Min-Zong; Cheng, Sy-Chi; Cho, Yi-Tzu; Shiea, Jentaie

2011-01-01

Highlights: → Ambient ionization technique allows the direct analysis of sample surfaces with little or no sample pretreatment. → We sort ambient ionization techniques into three main analytical strategies, direct ionization, direct desorption/ionization, and two-step ionization. → The underlying principles of operation, ionization processes, detecting mass ranges, sensitivity, and representative applications of these techniques are described and compared. - Abstract: Ambient ionization is a set of mass spectrometric ionization techniques performed under ambient conditions that allows the direct analysis of sample surfaces with little or no sample pretreatment. Using combinations of different types of sample introduction systems and ionization methods, several novel techniques have been developed over the last few years with many applications (e.g., food safety screening; detection of pharmaceuticals and drug abuse; monitoring of environmental pollutants; detection of explosives for antiterrorism and forensics; characterization of biological compounds for proteomics and metabolomics; molecular imaging analysis; and monitoring chemical and biochemical reactions). Electrospray ionization and atmospheric pressure chemical ionization are the two main ionization principles most commonly used in ambient ionization mass spectrometry. This tutorial paper provides a review of the publications related to ambient ionization techniques. We describe and compare the underlying principles of operation, ionization processes, detecting mass ranges, sensitivity, and representative applications of these techniques.

Processes engaged in the persistence in atmosphere of previously deposited artificial radionuclides

International Nuclear Information System (INIS)

Piga, Damien

2010-01-01

Since 1959, atmospheric sampling stations of the environmental radioactivity permanent observatory measure both natural and artificial radioactivity in ambient air. Nowadays, Cs-137 (30.07 years), an artificial radionuclide mainly issue from atmospheric weapons tests and several accidents, is still measured at trace level in the lower atmosphere although there is no significant release anymore. The aim of this study was to identify and characterize the processes which explain this persistence. Areas highly contaminated by Chernobylsk accident are the major contributors to the Cs-137 atmospheric persistence in France. In these areas, wildfires are the most significant resuspension processes during the dry season and can lead to long range transport events. Around 1013 Bq of Cs-137 are yearly resuspended by this process. In connection with significant increases of total suspended particles, Sahara is the second area involved in the atmospheric Cs-137 persistence due to dust transport events. The whole of these events has a mean contribution of around 1/3 of the Cs-137 background level at the French scale. The last identified process is the wood burning during winter. Even if its emission factor is low, spatial extent of source areas and quantities used at the season scale makes wood burning a significant process compared to ambient trace levels. At the French scale, around 1011 Bq of Cs-137 are yearly resuspended by this process. During this season, the decrease of ventilation conditions in the lower atmosphere leads to an increase of the background level whereas significant increases are due to long range transport events from Eastern Europe

Stable isotope measurement techniques for atmospheric greenhouse gases

International Nuclear Information System (INIS)

2002-01-01

The technical requirements to perform useful measurements of atmospheric greenhouse gas concentrations and of their isotope ratios are of direct relevance for all laboratories engaged in this field. A meaningful interpretation of isotopes in global models on sources and sinks of CO 2 and other greenhouse gases depends on strict laboratory protocols and data quality control measures ensuring comparable data in time and space. Only with this precondition met, the isotope techniques can serve as a potentially powerful method for reducing uncertainties in the global CO 2 budgets and for tracing pathways and interaction of terrestrial, oceanic, and atmospheric pools of carbon. This publication provides four contributions describing methods for the determination of the isotopic composition of trace gases in atmospheric air and in ice cores. These contributions have been indexed separately

Field measurements of horizontal forward motion velocities of terrestrial dust devils: Towards a proxy for ambient winds on Mars and Earth

Science.gov (United States)

Balme, M. R.; Pathare, A.; Metzger, S. M.; Towner, M. C.; Lewis, S. R.; Spiga, A.; Fenton, L. K.; Renno, N. O.; Elliott, H. M.; Saca, F. A.; Michaels, T. I.; Russell, P.; Verdasca, J.

2012-11-01

Dust devils - convective vortices made visible by the dust and debris they entrain - are common in arid environments and have been observed on Earth and Mars. Martian dust devils have been identified both in images taken at the surface and in remote sensing observations from orbiting spacecraft. Observations from landing craft and orbiting instruments have allowed the dust devil translational forward motion (ground velocity) to be calculated, but it is unclear how these velocities relate to the local ambient wind conditions, for (i) only model wind speeds are generally available for Mars, and (ii) on Earth only anecdotal evidence exists that compares dust devil ground velocity with ambient wind velocity. If dust devil ground velocity can be reliably correlated to the ambient wind regime, observations of dust devils could provide a proxy for wind speed and direction measurements on Mars. Hence, dust devil ground velocities could be used to probe the circulation of the martian boundary layer and help constrain climate models or assess the safety of future landing sites. We present results from a field study of terrestrial dust devils performed in the southwest USA in which we measured dust devil horizontal velocity as a function of ambient wind velocity. We acquired stereo images of more than a 100 active dust devils and recorded multiple size and position measurements for each dust devil. We used these data to calculate dust devil translational velocity. The dust devils were within a study area bounded by 10 m high meteorology towers such that dust devil speed and direction could be correlated with the local ambient wind speed and direction measurements. Daily (10:00-16:00 local time) and 2-h averaged dust devil ground speeds correlate well with ambient wind speeds averaged over the same period. Unsurprisingly, individual measurements of dust devil ground speed match instantaneous measurements of ambient wind speed more poorly; a 20-min smoothing window applied to

Single particle characterization, source apportionment, and aging effects of ambient aerosols in Southern California

Science.gov (United States)

Shields, Laura Grace

Composed of a mixture of chemical species and phases and existing in a variety of shapes and sizes, atmospheric aerosols are complex and can have serious influence on human health, the environment, and climate. In order to better understand the impact of aerosols on local to global scales, detailed measurements on the physical and chemical properties of ambient particles are essential. In addition, knowing the origin or the source of the aerosols is important for policymakers to implement targeted regulations and effective control strategies to reduce air pollution in their region. One of the most ground breaking techniques in aerosol instrumentation is single particle mass spectrometry (SPMS), which can provide online chemical composition and size information on the individual particle level. The primary focus of this work is to further improve the ability of one specific SPMS technique, aerosol time-of-flight mass spectrometry (ATOFMS), for the use of identifying the specific origin of ambient aerosols, which is known as source apportionment. The ATOFMS source apportionment method utilizes a library of distinct source mass spectral signatures to match the chemical information of the single ambient particles. The unique signatures are obtained in controlled source characterization studies, such as with the exhaust emissions of heavy duty diesel vehicles (HDDV) operating on a dynamometer. The apportionment of ambient aerosols is complicated by the chemical and physical processes an individual particle can undergo as it spends time in the atmosphere, which is referred to as "aging" of the aerosol. Therefore, the performance of the source signature library technique was investigated on the ambient dataset of the highly aged environment of Riverside, California. Additionally, two specific subsets of the Riverside dataset (ultrafine particles and particles containing trace metals), which are known to cause adverse health effects, were probed in greater detail. Finally

Greenhouse gases regional fluxes estimated from atmospheric measurements

International Nuclear Information System (INIS)

Messager, C.

2007-07-01

build up a new system to measure continuously CO 2 (or CO), CH 4 , N 2 O and SF 6 mixing ratios. It is based on a commercial gas chromatograph (Agilent 6890N) which have been modified to reach better precision. Reproducibility computed with a target gas on a 24 hours time step gives: 0.06 ppm for CO 2 , 1.4 ppb for CO, 0.7 ppb for CH 4 , 0.2 ppb for N 2 O and 0.05 ppt for SF 6 . The instrument's run is fully automated, an air sample analysis takes about 5 minutes. In July 2006, I install instrumentation on a telecommunication tall tower (200 m) situated near Orleans forest in Trainou, to monitor continuously greenhouse gases (CO 2 , CH 4 , N 2 O, SF 6 ), atmospheric tracers (CO, Radon-222) and meteorological parameters. Intake lines were installed at 3 levels (50, 100 and 180 m) and allow us to sample air masses along the vertical. Continuous measurement started in January 2007. I used Mace Head (Ireland) and Gif-sur-Yvette continuous measurements to estimate major greenhouse gases emission fluxes at regional scale. To make the link between atmospheric measurements and surface fluxes, we need to quantify dilution due to atmospheric transport. I used Radon-222 as tracer (radon tracer method) and planetary boundary layer heights estimates from ECMWF model (boundary layer budget method) to parameterize atmospheric transport. In both cases I compared results to available emission inventories. (author)

A new possibility of separate the natural and industrial components of the ambient radiation background

International Nuclear Information System (INIS)

Purghel, L.; Valcov, N.; Celarel, A.

1997-01-01

The ambient radiation background, sometimes considered as a gamma-ray background, is actually composed by a natural radiation field and an industrial radiation field, produced by nuclear facilities. This work presents a possibility to separate and to measure simultaneously both components by using the statistical discrimination method. As the statistical discrimination method is able to measure mixed radiation fields, characterized by essentially different statistical factors k = σ 2 / I (I - the mean value and σ 2 - the variance of the ionization current), this basic assumption of the method is checked, for the natural background and the gamma-ray checked, for natural background and the gamma-ray fields. The obtained value of the ratio k B / k γ = 9 has confirmed the validity of the statistical discrimination method as well as the assumption of a small contribution of the gamma-ray field to the ambient radiation background. Some estimations of the statistical uncertainties, associated with the measurement of two components of the ambient background field have been made. For a 10 liters, atmospheric pressure air - filled ionization chamber (or its equivalent, i.e. 2 liters, 5 atmospheres air -filled chamber) and a 30 s integration time constant, the minimum detectable absorbed dose rate of gamma-rays, for a 0.1 μ Gy / h natural background absorbed dose rate, is equal to 0.02 μ Gy / h. The statistical relative uncertainty of measurement for a 0.5 μ Gy / h absorbed dose rate gamma-ray field, corresponding to the admissible value of the equivalent dose rate of 0.6 μ Sv / h, for non-professional population is about 4 %. (authors)

Development of an atmospheric 214Bi measuring instrument

International Nuclear Information System (INIS)

1975-01-01

Part of the radiation environment encountered during airborne gamma ray surveys is produced by 214 Bi existing in the atmosphere. The 214 Bi atmospheric concentration changes with time and location, and should be measured to process the acquired data correctly. Three methods of atmospheric 214 Bi measurement are evaluated in this work. These are: (1) an 11 1 / 2 '' dia. x 4'' thick NaI(Tl) crystal shielded from ground radiation, (2) a negatively charged wire to collect radioactive ions, and (3) a high volume air sampler collecting particulate matter on filter paper. The shielded detector and filter paper methods yield good results with the shielded detector producing a factor of about 10 times higher counting rate. The charged wire method gave very low counting rates where the shielded detector counting rates were about a factor of 100 times higher, and the results did not correlate with the 214 Bi atmospheric concentration as determined by the other two methods. The theory necessary to understand the collection and decay of the airborne radioactivity using the charged wire and filter paper methods is developed

The photosynthesis - leaf nitrogen relationship at ambient and elevated atmospheric carbon dioxide: a meta-analysis

Energy Technology Data Exchange (ETDEWEB)

Andrew G. Peterson; J. Timothy Ball; Yiqi Luo; Christopher B. Field; Peter B. Reich; Peter S. Curtis; Kevin L. Griffin; Carla S Gunderson; Richard J. Norby; David T. Tissue; Manfred Forstreuter; Ana Rey; Christoph S. Vogel; CMEAL collaboration

1998-09-25

Estimation of leaf photosynthetic rate (A) from leaf nitrogen content (N) is both conceptually and numerically important in models of plant, ecosystem and biosphere responses to global change. The relationship between A and N has been studied extensively at ambient CO{sub 2} but much less at elevated CO{sub 2}. This study was designed to (1) assess whether the A-N relationship was more similar for species within than between community and vegetation types, and (2) examine how growth at elevated CO{sub 2} affects the A-N relationship. Data were obtained for 39 C{sub 3} species grown at ambient CO{sub 2} and 10 C{sub 3} species grown at ambient and elevated CO{sub 2}. A regression model was applied to each species as well as to species pooled within different community and vegetation types. Cluster analysis of the regression coefficients indicated that species measured at ambient CO{sub 2} did not separate into distinct groups matching community or vegetation type. Instead, most community and vegetation types shared the same general parameter space for regression coefficients. Growth at elevated CO{sub 2} increased photosynthetic nitrogen use efficiency for pines and deciduous trees. When species were pooled by vegetation type, the A-N relationship for deciduous trees expressed on a leaf-mass bask was not altered by elevated CO{sub 2}, while the intercept increased for pines. When regression coefficients were averaged to give mean responses for different vegetation types, elevated CO{sub 2} increased the intercept and the slope for deciduous trees but increased only the intercept for pines. There were no statistical differences between the pines and deciduous trees for the effect of CO{sub 2}. Generalizations about the effect of elevated CO{sub 2} on the A-N relationship, and differences between pines and deciduous trees will be enhanced as more data become available.

Simulated reaction of formaldehyde and ambient atmospheric particulate matter using a chamber

Institute of Scientific and Technical Information of China (English)

Yueyue Chen; Jia Liu; Jing Shang; Tong Zhu

2017-01-01

The reaction of HCHO with Beijing winter's real ambient particulate matter (PM) inside a 3.3 m3 Teflon Chamber was conducted in this study.NO2,O3 and H2O gases were removed from the ambient aerosol before entering into the chamber.The decays of HCHO were monitored (acetylacetone spectrophotometry method) during the reactions at different PM number concentrations (Na) and relative humidities (RHs),and the formed particulate formate was detected by IC and XPS techniques.The results showed that when RH was 10％-15％,the decay rate of HCHO in the chamber was higher with the existence of PM from relatively clean days (with number concentration (Na) ＜ 200,000 particle/L,0.35-22.5 μm) compared to dirty days (Na ＞ 200,000 particle/L,0.35-22.5 μm).When RH increased to 30％-45％,PM can hardly have significant influences on the decay of HCHO.The formations of formate on the reacted PM were consistent with the HCHO decay rates at different ambient PM Na and RH conditions.This is a first study related to the "real" ambient PM reacted with HCHO and suggested that in the clean and low RH days,PM could be an effective medium for the conversion of HCHO to formate.

Atmospheric acidity measurements on allegheny mountain and the origins of ambient acidity in the Northeastern United States

Science.gov (United States)

Pierson, William R.; Brachaczek, Wanda W.; Gorse, Robert A.; Japar, Steven M.; Norbeck, Joseph M.; Keeler, Gerald J.

Atmospheric acidity as HNO 3(g), SO 2(g), and aerosol H + was measured on Allegheny Mountain and Laurel Hill in southwest Pennsylvania in August 1983. The aerosol H + appeared to represent the net after H 2SO 4 reaction with NH 3(g). The resulting H +/SO 42- ratio depended on SO 42- concentration, approaching that of H 2SO 4 at the highest SO 42- concentrations. The atmosphere was acidic; the average concentrations of HNO 3 (78 nmole m -3) and aerosol H + (205 nmole m -3), NH 4+ (172 nmole m -3) and SO 42- (201 nmole m -3), and the dearth of NH 3( 2, with one 10-h period averaging 263 and 844 nmolem -3 for HNO 3 and aerosol H +, respectively. SO 2 added another 900 nmole m -3 (average) of potential H + acidity. HNO 3 and aerosol H + episodes were concurrent, on 7-8 day cycles, unrelated to SO 2 which existed more in short-lived bursts of apparently more local origin. NOx was sporadic like SO 2. Laurel and Allegheny, separated by 35.5 km, were essentially identical in aerosol SO 42-, and in aerosol H +, less so in HNO 3 and especially less so in SO 2; apparently, chemistry involving HNO 3 and aerosol H + or SO 42- was slow compared to inter-site transport times (1-2 h). From growth of bscat and decline of SO 2 during one instance of inter-site transport, daytime rate coefficients for SO 2 oxidation and SO 2 dry deposition were inferred to have been, respectively, ~ 0.05 and ⩽ 0.1 h -1. HNO 3 declined at night. Aerosol H + and SO 42- showed no significant diurnal variation, and O 3 showed very little; these observations, together with high PAN/NO x ratios, indicate that regional transport rather than local chemistry is governing. The O 3 concentration (average 56 ppb or 2178 nmolem -3) connotes an oxidizing atmosphere conducive to acid formation. Highest atmospheric acidity was associated with (1) slow westerly winds traversing westward SO 2 source areas, (2) local stagnation, or (3) regional transport around to the back side of a high pressure system. Low acidity

Comparisons of continuous atmospheric CH4, CO2 and N2O measurements - results from a travelling instrument campaign at Mace Head

International Nuclear Information System (INIS)

Vardag, S.N.; Hammer, S.; Levin, I.; O'Doherty, S.; Spain, T.G.; Wastine, B.; Jordan, A.

2014-01-01

A 2-month measurement campaign with a Fourier transform infrared analyser as a travelling comparison instrument (TCI) was performed at the Advanced Global Atmospheric Gases Experiment (AGAGE) and World Meteorological Organization (WMO) Global Atmosphere Watch (GAW) station at Mace Head, Ireland. The aim was to evaluate the compatibility of atmospheric methane (CH 4 ), carbon dioxide (CO 2 ) and nitrous oxide (N 2 O) measurements of the routine station instrumentation, consisting of a gas chromatograph (GC) for CH 4 and N 2 O as well as a cavity ring-down spectroscopy (CRDS) system for CH 4 and CO 2 . The advantage of a TCI approach for quality control is that the comparison covers the entire ambient air measurement system, including the sample intake system and the data evaluation process. For initial quality and performance control, the TCI was run in parallel with the Heidelberg GC before and after the measurement campaign at Mace Head. Median differences between the Heidelberg GC and the TCI were well within the WMO inter-laboratory compatibility target for all three greenhouse gases. At Mace Head, the median difference between the station GC and the TCI were -0.04 nmol mol -1 for CH 4 and -0.37 nmol mol -1 for N 2 O (GC-TCI). For N 2 O, a similar difference (-0.40 nmol mol -1 ) was found when measuring surveillance or working gas cylinders with both instruments. This suggests that the difference observed in ambient air originates from a calibration offset that could partly be due to a difference between the WMON2O X2006a reference scale used for the TCI and the Scripps Institution of Oceanography (SIO-1998) scale used at Mace Head and in the whole AGAGE network. Median differences between the CRDS G1301 and the TCI at Mace Head were 0.12 nmol mol -1 for CH 4 and 0.14 μmol mol -1 for CO 2 (CRDS G1301 - TCI). The difference between both instruments for CO 2 could not be explained, as direct measurements of calibration gases show no such difference. The CH 4

Twenty years of measurement of polycyclic aromatic hydrocarbons (PAHs) in UK ambient air by nationwide air quality networks.

Science.gov (United States)

Brown, Andrew S; Brown, Richard J C; Coleman, Peter J; Conolly, Christopher; Sweetman, Andrew J; Jones, Kevin C; Butterfield, David M; Sarantaridis, Dimitris; Donovan, Brian J; Roberts, Ian

2013-06-01

The impact of human activities on the health of the population and of the wider environment has prompted action to monitor the presence of toxic compounds in the atmosphere. Toxic organic micropollutants (TOMPs) are some of the most insidious and persistent of these pollutants. Since 1991 the United Kingdom has operated nationwide air quality networks to assess the presence of TOMPs, including polycyclic aromatic hydrocarbons (PAHs), in ambient air. The data produced in 2010 marked 20 years of nationwide PAH monitoring. This paper marks this milestone by providing a novel and critical review of the data produced since nationwide monitoring began up to the end of 2011 (the latest year for which published data is available), discussing how the networks performing this monitoring has evolved, and elucidating trends in the concentrations of the PAHs measured. The current challenges in the area and a forward look to the future of air quality monitoring for PAHs are also discussed briefly.

Southern Great Plains Atmospheric Radiation Measurement Site

Data.gov (United States)

Federal Laboratory Consortium — The Southern Great Plains Atmospheric Radiation Measurement Site (SGP-ARM) is the oldest and largest of DOE's Arm sites. It was established in 1992. It consists of...

Isotope measurement techniques for atmospheric methane

International Nuclear Information System (INIS)

Lowe, D.; White, J.; Levin, I.; Wahlen, M.; Miller, J.B.; Bergamaschi, P.

2002-01-01

Measurement techniques for the carbon isotopic composition of atmospheric methane (δ 13 C) are described in detail as applied in several leading institutions active in this field since many years. The standard techniques with offline sample preparation and subsequent measurement by dual inlet isotope ratio mass spectrometry (IRMS) are compared with continuous flow IRMS. The potential use of infrared absorption spectroscopy is briefly discussed. Details on quality control and calibration are provided. Basic analytical aspects for the measurement of other species, 2 H and 14 C, are also given. (author)

Evaluation and application of passive and active optical remote sensing methods for the measurement of atmospheric aerosol properties

Energy Technology Data Exchange (ETDEWEB)

Mielonen, T.

2010-07-01

Atmospheric aerosol particles affect the atmosphere's radiation balance by scattering and absorbing sunlight. Moreover, the particles act as condensation nuclei for clouds and affect their reflectivity. In addition, aerosols have negative health effects and they reduce visibility. Aerosols are emitted into the atmosphere from both natural and anthropogenic sources. Different types of aerosols have different effects on the radiation balance, thus global monitoring and typing of aerosols is of vital importance. In this thesis, several remote sensing methods used in the measurement of atmospheric aerosols are evaluated. Remote sensing of aerosols can be done with active and passive instruments. Passive instruments measure radiation emitted by the sun and the Earth while active instruments have their own radiation source, for example a black body radiator or laser. The instruments utilized in these studies were sun photometers (PFR, Cimel), lidars (POLLYXT, CALIOP), transmissiometer (OLAF) and a spectroradiometer (MODIS). Retrieval results from spaceborne instruments (MODIS, CALIOP) were evaluated with ground based measurements (PFR, Cimel). In addition, effects of indicative aerosol model assumptions on the calculated radiative transfer were studied. Finally, aerosol particle mass at the ground level was approximated from satellite measurements and vertical profiles of aerosols measured with a lidar were analyzed. For the evaluation part, these studies show that the calculation of aerosol induced attenuation of radiation based on aerosol size distribution measurements is not a trivial task. In addition to dry aerosol size distribution, the effect of ambient relative humidity on the size distribution and the optical properties of the aerosols need to be known in order to achieve correct results from the calculations. Furthermore, the results suggest that aerosol size parameters retrieved from passive spaceborne measurements depend heavily on surgace reflectance

Health Effects of Ambient Air Pollution in Developing Countries

OpenAIRE

Mannucci, Pier Mannuccio; Franchini, Massimo

2017-01-01

The deleterious effects of ambient air pollution on human health have been consistently documented by many epidemiologic studies worldwide, and it has been calculated that globally at least seven million deaths are annually attributable to the effects of air pollution. The major air pollutants emitted into the atmosphere by a number of natural processes and human activities include nitrogen oxides, volatile organic compounds, and particulate matter. In addition to the poor ambient air quality...

Atmospheric profiles from active space-based radio measurements

Science.gov (United States)

Hardy, Kenneth R.; Hinson, David P.; Tyler, G. L.; Kursinski, E. R.

1992-01-01

The paper describes determinations of atmospheric profiles from space-based radio measurements and the retrieval methodology used, with special attention given to the measurement procedure and the characteristics of the soundings. It is speculated that reliable profiles of the terrestrial atmosphere can be obtained by the occultation technique from the surface to a height of about 60 km. With the full complement of 21 the Global Positioning System (GPS) satellites and one GPS receiver in sun synchronous polar orbit, a maximum of 42 soundings could be obtained for each complete orbit or about 670 per day, providing almost uniform global coverage.

Raman Channel Temperature Measurement of SiC MESFET as a Function of Ambient Temperature and DC Power

Science.gov (United States)

Ponchak, George E.; Eldridge, Jeffrey J.; Krainsky, Isay L.

2009-01-01

Raman spectroscopy is used to measure the junction temperature of a Cree SiC MESFET as a function of the ambient temperature and DC power. The carrier temperature, which is approximately equal to the ambient temperature, is varied from 25 C to 450 C, and the transistor is biased with VDS=10V and IDS of 50 mA and 100 mA. It is shown that the junction temperature is approximately 52 and 100 C higher than the ambient temperature for the DC power of 500 and 1000 mW, respectively.

Relationship between Objective and Subjective Atmospheric Visibility and Its Influence on Willingness to Accept or Pay in China.

Directory of Open Access Journals (Sweden)

Kangkang Yu

Full Text Available This study is to distinguish the objective and subjective measures of atmospheric visibility, and investigate the relationship between the two measures as well as the effect on the people's behavioral intentions on air pollution in China. A mixed method was adopted in this study combining both lab experiments to measure objective atmospheric visibility and a questionnaire survey to measure subjective atmospheric visibility. The regression results show that: (a The people's perception of atmospheric visibility is based on objective information about the ambient air (Relative Humidity, PM2.5, Atmospheric Visibility and there are some turning points that could enable people to distinguish good and poor air quality; (b The people's perception of visibility has a significant effect on either their willingness-to-accept (WTA the visibility or on their willingness-to-pay (WTP for improving the air quality;

Absolute production rate measurements of nitric oxide by an atmospheric pressure plasma jet (APPJ)

International Nuclear Information System (INIS)

Pipa, A V; Bindemann, T; Foest, R; Kindel, E; Roepcke, J; Weltmann, K-D

2008-01-01

Tunable diode laser absorption spectroscopy (TDLAS) has been applied to measure the absolute production rate of NO molecules in the gas phase of an atmospheric pressure plasma jet (APPJ) operating at rf (13.56 MHz) in argon with small (up to 1%) admixtures of air. The resulting NO production rates were found to be in the range (0.1-80) x 10 -3 sccm or (0.05-35) x 10 18 molecules s -1 depending on the experimental conditions. Maximum rates were obtained at 0.2% air. For TDLAS measurements the APPJ was arranged inside an astigmatic multi-pass cell of Herriott type with 100 m absorption length. The insertion into a closed volume differs slightly from the normal, open operation with the jet propagating freely into air. Therefore, the measuring results are compared with optical emission of the open jet to verify equivalent experimental conditions. The dependence of the optical emission of NO (237 nm) on power and gas mixture has been measured. The similar shape of the dependence of absorption and emission signals gives evidence that the comparability of experimental conditions is sufficiently satisfied. It is concluded that the NO production rate of the APPJ in ambient air can be characterized using TDLAS and provides reliable results in spite of differing experimental conditions due to the set-up.

Air/surface exchange processes of mercury and their linkage to atmospheric pools

International Nuclear Information System (INIS)

Bahlmann, Enno; Ebinghaus, Ralf

2001-01-01

The atmospheric mercury cycle is strongly linked to the terrestrial, aquatic and biologic cycle of mercury via air/surface exchange processes. In order to quantify mercury fluxes from and to the atmosphere to predict local and regional source contributions the methods for flux measurements as well as the physicochemical factors controlling air/surface exchange processes must be assessed. We will describe methods for the determination of mercury and mercury species in ambient air which are basic for investigation of air/surface exchange processes. Further on we will describe approaches for studying the physicochemical factors controlling this processes by using a new laboratory flux measurement system. (author)

THE EFFECTS OF AMBIENT SCENT ON CONSUMER BEHAVIOR: A REVIEW OF THE LITERATURE

OpenAIRE

OLAHUT Meda Roxana; PLAIAS Ioan

2013-01-01

The main purpose of this paper is to present an extended literature review of relevant empirical studies which examine the effect of ambient scent on consumers' perception, consumers' emotions and consumers' behavioral responses in the context of retailing. Compared with other atmospheric stimuli (such as background music), ambient scent has received little attention from researchers. This paper is also concentrated on identifying de principal dimensions of ambient scent (presence versus abse...

THE EFFECTS OF AMBIENT SCENT ON CONSUMER BEHAVIOR: A REVIEW OF THE LITERATURE

OpenAIRE

OLAHUT Meda Roxana; PLAIAS Ioan

2013-01-01

The main purpose of this paper is to present an extended literature review of relevant empirical studies which examine the effect of ambient scent on consumers’ perception, consumers’ emotions and consumers’ behavioral responses in the context of retailing. Compared with other atmospheric stimuli (such as background music), ambient scent has received little attention from researchers. This paper is also concentrated on identifying de principal dimensions of ambient scent (presence versus abse...

A Continuous Flow System for the Measurement of Ambient Nitrogen Oxides [NO + NO] Using Rhodamine B Hydrazide as a Chemosensor

Directory of Open Access Journals (Sweden)

Pandurangappa Malingappa

2014-01-01

Full Text Available A new chemosensor has been used to monitor atmospheric nitrogen oxides [NO + NO 2 ] at parts per billion (ppb level. It is based on the catalytic reaction of nitrogen oxides with rhodamine B hydrazide (RBH to produce a colored compound through the hydrolysis of the amide bond of the molecule. A simple colorimeter has been used to monitor atmospheric nitrogen dioxide at ppb level. The air samples were purged through a sampling cuvette containing RBH solution using peristaltic pump. The proposed method has been successfully applied to monitor the ambient nitrogen dioxide levels at traffic junction points within the city limits and the results obtained are compared with the standard Griess-Ilosvay method.

Measurement of volatile plant compounds in field ambient air by thermal desorption-gas chromatography-mass spectrometry.

Science.gov (United States)

Cai, Xiao-Ming; Xu, Xiu-Xiu; Bian, Lei; Luo, Zong-Xiu; Chen, Zong-Mao

2015-12-01

Determination of volatile plant compounds in field ambient air is important to understand chemical communication between plants and insects and will aid the development of semiochemicals from plants for pest control. In this study, a thermal desorption-gas chromatography-mass spectrometry (TD-GC-MS) method was developed to measure ultra-trace levels of volatile plant compounds in field ambient air. The desorption parameters of TD, including sorbent tube material, tube desorption temperature, desorption time, and cold trap temperature, were selected and optimized. In GC-MS analysis, the selected ion monitoring mode was used for enhanced sensitivity and selectivity. This method was sufficiently sensitive to detect part-per-trillion levels of volatile plant compounds in field ambient air. Laboratory and field evaluation revealed that the method presented high precision and accuracy. Field studies indicated that the background odor of tea plantations contained some common volatile plant compounds, such as (Z)-3-hexenol, methyl salicylate, and (E)-ocimene, at concentrations ranging from 1 to 3400 ng m(-3). In addition, the background odor in summer was more abundant in quality and quantity than in autumn. Relative to previous methods, the TD-GC-MS method is more sensitive, permitting accurate qualitative and quantitative measurements of volatile plant compounds in field ambient air.

The exchange of acetaldehyde between plants and the atmosphere: Stable carbon isotope and flux measurements

Science.gov (United States)

Jardine, Kolby Jeremiah

The exchange of acetaldehyde between plant canopies and the atmosphere may significantly influence regional atmospheric chemistry and plant metabolism. While plants are known to both produce and consume acetaldehyde, the exchange of this compound with forested ecosystems is complicated by physical, biological, and chemical processes that range from being poorly understood to completely unknown. This precludes a quantitative understanding of acetaldehyde exchange rates between the atmosphere and the biosphere. In this study, the processes controlling the exchange of acetaldehyde with plant canopies was investigated using concentration, flux, and natural abundance 13C measurements of gas phase acetaldehyde from individual plants, soils, and entire ecosystems. Although previously only considered important in anoxic tissues, it was discovered that acetaldehyde is produced and consumed in leaves through ethanolic fermentation coupled to the pyruvate dehydrogenase bypass system under normal aerobic conditions. These coupled pathways determine the acetaldehyde compensation point, a major factor controlling its exchange with the atmosphere. Carbon isotope analysis suggests a new pathway for acetaldehyde production from plants under stress involving the peroxidation of membrane fatty acids. This pathway may be a major source of acetaldehyde to the atmosphere from plants under biotic and abiotic stresses. Plant stomata were found to be the dominant pathway for the exchange of acetaldehyde with the atmosphere with stomatal conductance influencing both emission and uptake fluxes. In addition, increasing temperature and solar radiation was found to increase the compensation point by increasing the rates of acetaldehyde production relative to consumption. Under ambient conditions, bare soil was neutral to the exchange of acetaldehyde while senescing and decaying leaves were found to be strong source of acetaldehyde to the atmosphere due to increased decomposition processes and

Measurement and modeling of shortwave irradiance components in cloud-free atmospheres

Energy Technology Data Exchange (ETDEWEB)

Halthore, R.N.

1999-08-04

Atmosphere scatters and absorbs incident solar radiation modifying its spectral content and decreasing its intensity at the surface. It is very useful to classify the earth-atmospheric solar radiation into several components--direct solar surface irradiance (E{sub direct}), diffuse-sky downward surface irradiance (E{sub diffuse}), total surface irradiance, and upwelling flux at the surface and at the top-of-the atmosphere. E{sub direct} depends only on the extinction properties of the atmosphere without regard to details of extinction, namely scattering or absorption; furthermore it can be accurately measured to high accuracy (0.3%) with the aid of an active cavity radiometer (ACR). E{sub diffuse} has relatively larger uncertainties both in its measurement using shaded pyranometers and in model estimates, owing to the difficulty in accurately characterizing pyranometers and in measuring model inputs such as surface reflectance, aerosol single scattering albedo, and phase function. Radiative transfer model simulations of the above surface radiation components in cloud-free skies using measured atmospheric properties show that while E{sub direct} estimates are closer to measurements, E{sub diffuse} is overestimated by an amount larger than the combined uncertainties in model inputs and measurements, illustrating a fundamental gap in the understanding of the magnitude of atmospheric absorption in cloud-free skies. The excess continuum type absorption required to reduce the E{sub diffuse} model overestimate ({approximately}3--8% absorptance) would significantly impact climate prediction and remote sensing. It is not clear at present what the source for this continuum absorption is. Here issues related to measurements and modeling of the surface irradiance components are discussed.

Detailed characterization of a Comparative Reactivity Method (CRM) instrument for ambient OH reactivity measurements: experiments vs. modeling

Science.gov (United States)

Michoud, Vincent; Locoge, Nadine; Dusanter, Sébastien

2015-04-01

The Hydroxyl radical (OH) is the main daytime oxidant in the troposphere, leading to the oxidation of Volatile Organic Compounds (VOCs) and the formation of harmful pollutants such as ozone (O3) and Secondary Organic Aerosols (SOA). While OH plays a key role in tropospheric chemistry, recent studies have highlighted that there are still uncertainties associated with the OH budget, i.e the identification of sources and sinks and the quantification of production and loss rates of this radical. It has been demonstrated that ambient measurements of the total OH loss rate (also called total OH reactivity) can be used to identify and reduce these uncertainties. In this context, the Comparative Reactivity Method (CRM), developed by Sinha et al. (ACP, 2008), is a promising technique to measure total OH reactivity in ambient air and has already been used during several field campaigns. This technique relies on monitoring competitive reactions of OH with ambient trace gases and a reference compound (pyrrole) in a sampling reactor to derive ambient OH reactivity. However, this technique requires a complex data processing chain that has yet to be carefully investigated in the laboratory. In this study, we present a detailed characterization of a CRM instrument developed at Mines Douai, France. Experiments have been performed to investigate the dependence of the CRM response on humidity, ambient NOx levels, and the pyrrole-to-OH ratio inside the sampling reactor. Box modelling of the chemistry occurring in the reactor has also been performed to assess our theoretical understanding of the CRM measurement. This work shows that the CRM response is sensitive to both humidity and NOx, which can be accounted for during data processing using parameterizations depending on the pyrrole-to-OH ratio. The agreement observed between laboratory studies and model results suggests a good understanding of the chemistry occurring in the sampling reactor and gives confidence in the CRM

ORGANOCHLORINE PESTICIDES IN THE AMBIENT AIR OF MEXICO

Science.gov (United States)

Recent and past use of organochlorine pesticides (OCPs) in Mexico has resulted in concentrations in ambient air that are 1-2 orders of magnitude above levels in the Great Lakes region. Atmospheric transport from Mexico and Central America may be contributing significant amounts ...

Atmospheric Radiation Measurement Program plan

International Nuclear Information System (INIS)

1990-02-01

In order to understand energy's role in anthropogenic global climate change, significant reliance is being placed on General Circulation Models (GCMs). A major goal is to foster the development of GCMs capable of predicting the timing and magnitude of greenhouse gas-induced global warming and the regional effects of such warming. The Atmospheric Radiation Measurement (ARM) Program will contribute to the Department of Energy goal by improving the treatment of cloud radiative forcing and feedbacks in GCMs. Two issues will be addressed: the radiation budget and its spectral dependence and the radiative and other properties of clouds. The experimental objective of the ARM Program is to characterize empirically the radiative processes in the Earth's atmosphere with improved resolution and accuracy. A key to this characterization is the effective treatment of cloud formation and cloud properties in GCMs. Through this characterization of radiative properties, it will be possible to understand both the forcing and feedback effects. 19 refs., 4 figs., 2 tabs

The possible direct use of satellite radiance measurements by the Atmospheric Radiation Measurement Program

International Nuclear Information System (INIS)

1993-03-01

The Atmospheric Radiation Measurement (ARM) Program is a major research program initiated by the Department of Energy to improve our understanding of radiative and cloud processes critical to predicting the Earth's climate and its changes. Central to this concept is the use of four to six intensively instrumented sites for long-term study and characterization of the processes of interest. The instrumentation suites will include ground-based, high-accuracy radiometers for measuring the short and longwave surface flux, as well as an extensive set of ground-and air-based instrumentation for characterizing the intervening atmospheric column. Satellite-based measurements are expected to play a very important role in providing top-of-the-atmosphere measurements. In this study, we examine the possibility of comparing ARM outputs directly with satellite measurements, thereby ensuring the independence of these two important data sets. Thus we focused on what do satellites really measure and how well do they measure it. On what can we do about the general lack of adequate visible channel calibration. On what is the best way for ARM to obtain near-real-time access to this unprocessed data. And on what is the optimum way for ARM to make use of satellite data

Ambient and laboratory observations of organic ammonium salts in PM1.

Science.gov (United States)

Schlag, P; Rubach, F; Mentel, T F; Reimer, D; Canonaco, F; Henzing, J S; Moerman, M; Otjes, R; Prévôt, A S H; Rohrer, F; Rosati, B; Tillmann, R; Weingartner, E; Kiendler-Scharr, A

2017-08-24

Ambient measurements of PM 1 aerosol chemical composition at Cabauw, the Netherlands, implicate higher ammonium concentrations than explained by the formation of inorganic ammonium salts. This additional particulate ammonium is called excess ammonium (e NH 4 ). Height profiles over the Cabauw Experimental Site for Atmospheric Research (CESAR) tower, of combined ground based and airborne aerosol mass spectrometric (AMS) measurements on a Zeppelin airship show higher concentrations of e NH 4 at higher altitudes compared to the ground. Through flights across the Netherlands, the Zeppelin based measurements furthermore substantiate e NH 4 as a regional phenomenon in the planetary boundary layer. The excess ammonium correlates with mass spectral signatures of (di-)carboxylic acids, making a heterogeneous acid-base reaction the likely process of NH 3 uptake. We show that this excess ammonium was neutralized by the organic fraction forming particulate organic ammonium salts. We discuss the significance of such organic ammonium salts for atmospheric aerosols and suggest that NH 3 emission control will have benefits for particulate matter control beyond the reduction of inorganic ammonium salts.

Air quality and Atmospheric resources: Phase 1: Background document

International Nuclear Information System (INIS)

2001-01-01

The Environment and Sustainable Development Indicators (ESDI) initiative, under the umbrella of the National Round Table on the Environment and the Economy (NRTEE), commissioned a study for the evaluation and the development of sustainable development indicators (SDIs) in the field of air quality and atmospheric resources. The report contained key information with regard to each indicator or indicator set, and no comprehensive comparative analysis was performed. The report was designed to be used as a technical reference. Where appropriate, SDIs developed by foreign organizations were included. The emphasis of the report was: (1) ambient air quality and human health effects, (2) air emissions having transboundary or global implications for ecosystem health and human health, and (3) demand on the atmosphere for environmental services. The bulk of the research was conducted on the Internet. The report was divided into three sections. A review of the availability of SDIs based on ambient air quality measures was discussed in the first section, while the second section was devoted to the availability of SDIs based on pollutant emission levels. The last section contained a systematic review of those SDIs used or being proposed along with the supporting data available to calculate SDI values. Some observations were also made touching on topics such as the abundance of ambient air quality information, the abundance of pollutant emissions information, the linkages between emissions and ambient air quality, the absence of forecasting, the indoor air quality gap, and the connections to human health. refs., 1 fig

Experimental study of the influence of atmospheric conditions on the performance of natural draft dry cooling towers

International Nuclear Information System (INIS)

Markoczy, G.; Staempfli, E.

1977-08-01

The heat dissipation of cooling towers is influenced by atmospheric conditions. In order to establish these influences EIR conducted measurements on a natural draft dry cooling tower. During two measuring campaigns with a duration of total 10 weeks the performance of the cooling tower, the ambient air temperatures, the wind velocities and directions as well as air temperature at the top of the tower and in front of the heat exchangers were continuously measured and registered. The results achieved enable the quantitative description of the influence of the ambient air temperature, wind and temperature inversion on the performance of natural draft dry cooling towers. (Auth.)

Effects of initiating anaerobic digestion of layer-hen poultry dung at sub-atmospheric pressure

Directory of Open Access Journals (Sweden)

Chima C. Ngumah

2013-12-01

Full Text Available This study investigated the effects of initiating anaerobic digestion (AD of dry layer-hen poultry dung at the sub-atmospheric pressure of -30 cmHg on biodegradation, biogasification, and biomethanation. The setup was performed as a batch process at an average ambient temperature of 29±2 0C and a retention time of 15 days. Comparisons were made with two other experiments which were both begun at ambient atmospheric pressure; one was inoculated with digestate from a previous layer-hen dung AD, while the other was not inoculated. The bioreactors initiated at sub-atmospheric pressure, ambient atmospheric pressure without inoculum, and ambient atmospheric pressure with inoculum showed the following for biogas and biomethane yields respectively: 16.8 cm3 g-1 VS and 15.46 cm3 g 1 VS, 25.10 cm3 g-1 VS and 12.85 cm3 g-1 VS, 21.44 cm3 g-1 VS and 14.88 cm3 g 1 VS. In the same order, after AD, the following values were recorded for volatile solids and total viable counts (prokaryotes and fungi in the digestates: 40.33% and 23.22 x 106 cfu mL-1, 43.42% and 22.17 x 106 cfu mL-1, 41.11% and 13.3 x 106 cfu mL-1. The feedstock showed values of 83.93% and 3.98 x 106 cfu mL-1 for volatile solids and total viable count respectively. There was a slight difference in the volatile solids of the digestates of the three bioreactors after AD. The pH recorded for the feedstock slurry before AD was 7.9 at 30oC, while after AD, the digestates from all the three bioreactors showed the same pH of 5.9 at 29 0C. Statistical analysis using ANOVA showed no significant difference in biogas yields of the feedstock for the three bioreactors (A, B, C. ANOVA showed no significant difference for biomethane yields in the bioreactors initiated at sub-atmospheric pressure and for those initiated at ambient atmospheric pressure with inoculums. However, it showed significant difference in the bioreactor initiated at sub-atmospheric pressure and that initiated at ambient atmospheric

Brachial artery responses to ambient pollution, temperature, and humidity in people with type 2 diabetes: a repeated-measures study.

Science.gov (United States)

Zanobetti, Antonella; Luttmann-Gibson, Heike; Horton, Edward S; Cohen, Allison; Coull, Brent A; Hoffmann, Barbara; Schwartz, Joel D; Mittleman, Murray A; Li, Yongsheng; Stone, Peter H; de Souza, Celine; Lamparello, Brooke; Koutrakis, Petros; Gold, Diane R

2014-03-01

Extreme weather and air pollution are associated with increased cardiovascular risk in people with diabetes. In a population with diabetes, we conducted a novel assessment of vascular brachial artery responses both to ambient pollution and to weather (temperature and water vapor pressure, a measure of humidity). Sixty-four 49- to 85-year-old Boston residents with type 2 diabetes completed up to five study visits (279 repeated measures). Brachial artery diameter (BAD) was measured by ultrasound before and after brachial artery occlusion [i.e., flow-mediated dilation (FMD)] and before and after nitroglycerin-mediated dilation (NMD). Ambient concentrations of fine particulate mass (PM2.5), black carbon (BC), organic carbon (OC), elemental carbon, particle number, and sulfate were measured at our monitoring site; ambient concentrations of carbon monoxide, nitrogen dioxide, and ozone were obtained from state monitors. Particle exposure in the home and during each trip to the clinic (home/trip exposure) was measured continuously and as a 5-day integrated sample. We used linear models with fixed effects for participants, adjusting for date, season, temperature, and water vapor pressure on the day of each visit, to estimate associations between our outcomes and interquartile range increases in exposure. Baseline BAD was negatively associated with particle pollution, including home/trip-integrated BC (-0.02 mm; 95% CI: -0.04, -0.003, for a 0.28 μg/m3 increase in BC), OC (-0.08 mm; 95% CI: -0.14, -0.03, for a 1.61 μg/m3 increase) as well as PM2.5, 5-day average ambient PM2.5, and BC. BAD was positively associated with ambient temperature and water vapor pressure. However, exposures were not consistently associated with FMD or NMD. Brachial artery diameter, a predictor of cardiovascular risk, decreased in association with particle pollution and increased in association with ambient temperature in our study population of adults with type 2 diabetes. Zanobetti A, Luttmann

Health Effects of Ambient Air Pollution in Developing Countries.

Science.gov (United States)

Mannucci, Pier Mannuccio; Franchini, Massimo

2017-09-12

The deleterious effects of ambient air pollution on human health have been consistently documented by many epidemiologic studies worldwide, and it has been calculated that globally at least seven million deaths are annually attributable to the effects of air pollution. The major air pollutants emitted into the atmosphere by a number of natural processes and human activities include nitrogen oxides, volatile organic compounds, and particulate matter. In addition to the poor ambient air quality, there is increasing evidence that indoor air pollution also poses a serious threat to human health, especially in low-income countries that still use biomass fuels as an energy resource. This review summarizes the current knowledge on ambient air pollution in financially deprived populations.

TRANC - a novel fast-response converter to measure total reactive atmospheric nitrogen

Science.gov (United States)

Marx, O.; Brümmer, C.; Ammann, C.; Wolff, V.; Freibauer, A.

2012-05-01

The input and loss of plant available nitrogen (reactive nitrogen: Nr) from/to the atmosphere can be an important factor for the productivity of ecosystems and thus for its carbon and greenhouse gas exchange. We present a novel converter for reactive nitrogen (TRANC: Total Reactive Atmospheric Nitrogen Converter), which offers the opportunity to quantify the sum of all airborne reactive nitrogen compounds (∑Nr) in high time resolution. The basic concept of the TRANC is the full conversion of all Nr to nitrogen monoxide (NO) within two reaction steps. Initially, reduced Nr compounds are being oxidised, and oxidised Nr compounds are thermally converted to lower oxidation states. Particulate Nr is being sublimated and oxidised or reduced afterwards. In a second step, remaining higher nitrogen oxides or those generated in the first step are catalytically converted to NO with carbon monoxide used as reduction gas. The converter is combined with a fast response chemiluminescence detector (CLD) for NO analysis and its performance was tested for the most relevant gaseous and particulate Nr species under both laboratory and field conditions. Recovery rates during laboratory tests for NH3 and NO2 were found to be 95 and 99%, respectively, and 97% when the two gases were combined. In-field longterm stability over an 11-month period was approved by a value of 91% for NO2. Effective conversion was also found for ammonium and nitrate containing particles. The recovery rate of total ambient Nr was tested against the sum of individual measurements of NH3, HNO3, HONO, NH4+, NO3-, and NOx using a combination of different well-established devices. The results show that the TRANC-CLD system precisely captures fluctuations in ∑Nr concentrations and also matches the sum of all individual Nr compounds measured by the different single techniques. The TRANC features a specific design with very short distance between the sample air inlet and the place where the thermal and catalytic

Algorithms in ambient intelligence

NARCIS (Netherlands)

Aarts, E.H.L.; Korst, J.H.M.; Verhaegh, W.F.J.; Weber, W.; Rabaey, J.M.; Aarts, E.

2005-01-01

We briefly review the concept of ambient intelligence and discuss its relation with the domain of intelligent algorithms. By means of four examples of ambient intelligent systems, we argue that new computing methods and quantification measures are needed to bridge the gap between the class of

IMPACT OF ATMOSPHERIC CHROMATIC EFFECTS ON WEAK LENSING MEASUREMENTS

International Nuclear Information System (INIS)

Meyers, Joshua E.; Burchat, Patricia R.

2015-01-01

Current and future imaging surveys will measure cosmic shear with statistical precision that demands a deeper understanding of potential systematic biases in galaxy shape measurements than has been achieved to date. We use analytic and computational techniques to study the impact on shape measurements of two atmospheric chromatic effects for ground-based surveys such as the Dark Energy Survey and the Large Synoptic Survey Telescope (LSST): (1) atmospheric differential chromatic refraction and (2) wavelength dependence of seeing. We investigate the effects of using the point-spread function (PSF) measured with stars to determine the shapes of galaxies that have different spectral energy distributions than the stars. We find that both chromatic effects lead to significant biases in galaxy shape measurements for current and future surveys, if not corrected. Using simulated galaxy images, we find a form of chromatic “model bias” that arises when fitting a galaxy image with a model that has been convolved with a stellar, instead of galactic, PSF. We show that both forms of atmospheric chromatic biases can be predicted (and corrected) with minimal model bias by applying an ordered set of perturbative PSF-level corrections based on machine-learning techniques applied to six-band photometry. Catalog-level corrections do not address the model bias. We conclude that achieving the ultimate precision for weak lensing from current and future ground-based imaging surveys requires a detailed understanding of the wavelength dependence of the PSF from the atmosphere, and from other sources such as optics and sensors. The source code for this analysis is available at https://github.com/DarkEnergyScienceCollaboration/chroma

IMPACT OF ATMOSPHERIC CHROMATIC EFFECTS ON WEAK LENSING MEASUREMENTS

Energy Technology Data Exchange (ETDEWEB)

Meyers, Joshua E.; Burchat, Patricia R., E-mail: jmeyers314@gmail.com [Kavli Institute for Particle Astrophysics and Cosmology, Department of Physics, Stanford University, Stanford, CA 94305 (United States)

2015-07-10

Current and future imaging surveys will measure cosmic shear with statistical precision that demands a deeper understanding of potential systematic biases in galaxy shape measurements than has been achieved to date. We use analytic and computational techniques to study the impact on shape measurements of two atmospheric chromatic effects for ground-based surveys such as the Dark Energy Survey and the Large Synoptic Survey Telescope (LSST): (1) atmospheric differential chromatic refraction and (2) wavelength dependence of seeing. We investigate the effects of using the point-spread function (PSF) measured with stars to determine the shapes of galaxies that have different spectral energy distributions than the stars. We find that both chromatic effects lead to significant biases in galaxy shape measurements for current and future surveys, if not corrected. Using simulated galaxy images, we find a form of chromatic “model bias” that arises when fitting a galaxy image with a model that has been convolved with a stellar, instead of galactic, PSF. We show that both forms of atmospheric chromatic biases can be predicted (and corrected) with minimal model bias by applying an ordered set of perturbative PSF-level corrections based on machine-learning techniques applied to six-band photometry. Catalog-level corrections do not address the model bias. We conclude that achieving the ultimate precision for weak lensing from current and future ground-based imaging surveys requires a detailed understanding of the wavelength dependence of the PSF from the atmosphere, and from other sources such as optics and sensors. The source code for this analysis is available at https://github.com/DarkEnergyScienceCollaboration/chroma.

An experimental verification of the compensation of length change of line scales caused by ambient air pressure

International Nuclear Information System (INIS)

Takahashi, Akira; Miwa, Nobuharu

2010-01-01

Line scales are used as a working standard of length for the calibration of optical measuring instruments such as profile projectors, measuring microscopes and video measuring systems. The authors have developed a one-dimensional calibration system for line scales to obtain a lower uncertainty of measurement. The scale calibration system, named Standard Scale Calibrator SSC-05, employs a vacuum interferometer system for length measurement, a 633 nm iodine-stabilized He–Ne laser to calibrate the oscillating frequency of the interferometer laser light source and an Abbe's error compensation structure. To reduce the uncertainty of measurement, the uncertainty factors of the line scale and ambient conditions should not be neglected. Using the length calibration system, the expansion and contraction of a line scale due to changes in ambient air pressure were observed and the measured scale length was corrected into the length under standard atmospheric pressure, 1013.25 hPa. Utilizing a natural rapid change in the air pressure caused by a tropical storm (typhoon), we carried out an experiment on the length measurement of a 1000 mm long line scale made of glass ceramic with a low coefficient of thermal expansion. Using a compensation formula for the length change caused by changes in ambient air pressure, the length change of the 1000 mm long line scale was compensated with a standard deviation of less than 1 nm

Global atmospheric particle formation from CERN CLOUD measurements

Science.gov (United States)

Dunne, Eimear M.; Gordon, Hamish; Carslaw, Kenneth S.

2017-04-01

New particle formation (or nucleation) is acknowledged as a significant source of climate-relevant aerosol throughout the atmosphere. However, performing atmospherically relevant nucleation experiments in a laboratory setting is extremely challenging. As a result, until now, the parameterisations used to represent new particle formation in global aerosol models were largely based on in-situ observations or theoretical nucleation models, and usually only represented the binary H2SO4-H2O system. Several different chemicals can affect particle formation rates, even at extremely low trace concentrations, which are technically challenging to measure directly. Nucleation rates also respond to environmental changes in e.g. temperature in a highly non-linear fashion. The CERN CLOUD experiment was designed to provide the most controlled and accurate nucleation rate measurements to date, over the full range of free tropospheric temperatures and down to sulphuric acid concentrations of the order of 105 cm-3. We will present a parameterisation of inorganic nucleation rates for use in global models, based on these measurements, which includes four separate nucleation pathways: binary neutral, binary ion-induced, ternary neutral, and ternary ion-induced. Both inorganic and organic nucleation parameterisations derived from CLOUD measurements have been implemented in the GLOMAP global aerosol model. The parameterisations depend on temperature and on concentrations of sulphuric acid, ammonia, organic vapours, and ions. One of CLOUD's main original goals was to determine the sensitivity of atmospheric aerosol to changes in the nucleation rate over a solar cycle. We will show that, in a present-day atmosphere, the changes in climate-relevant aerosol (in the form of cloud-level cloud condensation nuclei) over a solar cycle are on average about 0.1%, with local changes of less than 1%. In contrast, anthropogenic changes in ammonia since pre-industrial times were estimated to have a

Measuring variations of δ18O and δ2H in atmospheric water vapour using two commercial laser-based spectrometers: an instrument characterisation study

Directory of Open Access Journals (Sweden)

S. Pfahl

2012-07-01

Full Text Available Variations of stable water isotopes in water vapour have become measurable at a measurement frequency of about 1 Hz in recent years using novel laser spectroscopic techniques. This enables us to perform continuous measurements for process-based investigations of the atmospheric water cycle at the time scales relevant for synoptic and mesoscale meteorology. An important prerequisite for the interpretation of data from automated field measurements lasting for several weeks or months is a detailed knowledge about instrument properties and the sources of measurement uncertainty. We present here a comprehensive characterisation and comparison study of two commercial laser spectroscopic systems based on cavity ring-down spectroscopy (Picarro and off-axis integrated cavity output spectroscopy (Los Gatos Research. The uncertainty components of the measurements were first assessed in laboratory experiments, focussing on the effects of (i water vapour mixing ratio, (ii measurement stability, (iii uncertainties due to calibration and (iv response times of the isotope measurements due to adsorption-desorption processes on the tubing and measurement cavity walls. Based on the experience from our laboratory experiments, we set up a one-week field campaign for comparing measurements of the ambient isotope signals from the two laser spectroscopic systems. The optimal calibration strategy determined for both instruments was applied as well as the correction functions for water vapour mixing ratio effects. The root mean square difference between the isotope signals from the two instruments during the field deployment was 2.3‰ for δ2H, 0.5‰ for δ18O and 3.1‰ for deuterium excess. These uncertainty estimates from field measurements compare well to those found in the laboratory experiments. The present quality of measurements from laser spectroscopic instruments combined with a calibration system opens new possibilities for investigating the atmospheric

PALOMA : An instrument to measure the molecular, elemental and isotopic composition of Mars atmosphere from a landed platform (MSL 09, EXOMARS)

Science.gov (United States)

Chassefière, E.; Paloma Team

2003-04-01

required level of vacuum in the separation line and in the spectrometer, a small additional stand-alone sensor for radon and its short-lived daughters measurement. It is designed to work during one full Martian year, in order to perform accurate measurements of the atmospheric composition and its seasonal, and more generally temporal, variations. The gas is sampled directly from the ambient atmosphere, without need for an external sample distribution system. The main parameters of PALOMA are 6.5 kg, 20 W (peak value : 30 W), 4 kb/day (peak value : 15 kb/day).

Water vapor retrieval from near-IR measurements of polarized scanning atmospheric corrector

Science.gov (United States)

Qie, Lili; Ning, Yuanming; Zhang, Yang; Chen, Xingfeng; Ma, Yan; Li, Zhengqiang; Cui, Wenyu

2018-02-01

Water vapor and aerosol are two key atmospheric factors effecting the remote sensing image quality. As water vapor is responsible for most of the solar radiation absorption occurring in the cloudless atmosphere, accurate measurement of water content is important to not only atmospheric correction of remote sensing images, but also many other applications such as the study of energy balance and global climate change, land surface temperature retrieval in thermal remote sensing. A multi-spectral, single-angular, polarized radiometer called Polarized Scanning Atmospheric Corrector (PSAC) were developed in China, which are designed to mount on the same satellite platform with the principle payload and provide essential parameters for principle payload image atmospheric correction. PSAC detect water vapor content via measuring atmosphere reflectance at water vapor absorbing channels (i.e. 0.91 μm) and nearby atmospheric window channel (i.e. 0.865μm). A near-IR channel ratio method was implemented to retrieve column water vapor (CWV) amount from PSAC measurements. Field experiments were performed at Yantai, in Shandong province of China, PSAC aircraft observations were acquired. The comparison between PSAC retrievals and ground-based Sun-sky radiometer measurements of CWV during the experimental flights illustrates that this method retrieves CWV with relative deviations ranging from 4% 13%. This method retrieve CWV more accurate over land than over ocean, as the water reflectance is low.

Torque and Axial Loading Physics for Measuring Atmospheric Icing Load and Icing Rate

OpenAIRE

Mughal, Umair Najeeb; Virk, Muhammad Shakeel

2015-01-01

Measuring icing load and icing rate are important parameters for an atmospheric icing sensor. A new icing sensor has recently been designed and developed at Narvik University College for measuring atmospheric icing rate, icing load and icing type. Unlike the existing atmospheric icing sensors commercially available in market, which uses the axial loading for measuring icing load and icing rate, this new sensory system measures icing load and icing rate using the torque loading physics. The pe...

Medição de desempenho ambiental baseada em método multicriterial de apoio à decisão: estudo de caso na indústria automotiva Environmental performance measurement supported by a multicriterial approach: a case study in a manufacturing operation in the automotive industry

Directory of Open Access Journals (Sweden)

Sheila Oliveira de Castro da Luz

2006-12-01

Full Text Available Este artigo apresenta e discute um estudo de caso sobre medição de desempenho ambiental (MDA baseada em um método multicriterial de apoio à decisão, o AHP. A medição foi feita em uma operação de manufatura da indústria automotiva, cujo Sistema de Gestão Ambiental (SGA é certificado conforme a norma ISO 14001:2004. A metodologia foi desenvolvida de forma a viabilizar a sua extensão a outras indústrias ou tipos de operação. O artigo inicia apresentando uma discussão sobre desempenho empresarial e ambiental, justificando a necessidade de um índice para medir e comunicar este desempenho. Cita-se o método multicriterial usado e, a seguir, propõe-se a metodologia de medição, na qual se formulam construtos de sustentação do índice, calculam-se importâncias relativas dos construtos e especificam-se os indicadores. O índice foi calculado para o desempenho atual, chegando-se a um desempenho ambiental próximo a 85% do máximo possível. Os construtos empregados na medição são: resíduos sólidos; efluentes; emissões atmosféricas; uso de recursos naturais; e gestão ambiental. As principais oportunidades de melhoria ambiental são reduções no uso de recursos naturais e em emiss��es atmosféricas.This paper presents and discusses a case concerning environmental performance measurement (MDA, in which a multicriterial approach, the AHP, was used. The measurement took place in a manufacturing operation in the automotive industry, whose environmental management system (SGA is certified according to ISO 14001: 2004. The methodology was developed in such a way that it is feasible to reproduce it in other industries or operations. The paper discusses business and environmental performance, justifying the need for a numerical index, in order to establish such performances. We propose the measurement methodology, in which we formulate hierarchical constructs for sustaining the index, weighed by the AHP and measured by indicators

Evaluation of Routine Atmospheric Sounding Measurements Using Unmanned Systems (ERASMUS) Field Campaign Report

Energy Technology Data Exchange (ETDEWEB)

de Boer, Gijs [Univ. of Colorado, Boulder, CO (United States). Cooperative Inst. for Research in Environmental Sciences (CIRES); Lawrence, Dale [Univ. of Colorado, Boulder, CO (United States); Palo, Scott [Univ. of Colorado, Boulder, CO (United States); Argrow, Brian [Univ. of Colorado, Boulder, CO (United States); LoDolce, Gabriel [Univ. of Colorado, Boulder, CO (United States); Curry, Nathan [Univ. of Colorado, Boulder, CO (United States); Weibel, Douglas [Univ. of Colorado, Boulder, CO (United States); Finnamore, W [Univ. of Colorado, Boulder, CO (United States); D' Amore, P [Univ. of Colorado, Boulder, CO (United States); Borenstein, Steven [Univ. of Colorado, Boulder, CO (United States); Nichols, Tevis [Univ. of Colorado, Boulder, CO (United States); Elston, Jack [Blackswift Technologies, Boulder, CO (United States); Ivey, Mark [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States); Bendure, Al [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States); Schmid, Beat [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Long, Chuck [National Oceanic and Atmospheric Administration (NOAA), Boulder, CO (United States). Earth System Research Lab.; Telg, Hagen [Univ. of Colorado, Boulder, CO (United States). Cooperative Inst. for Research in Environmental Sciences (CIRES); Gao, Rushan [National Oceanic and Atmospheric Administration (NOAA), Boulder, CO (United States). Earth System Research Lab.; Hock, T [National Center for Atmospheric Research, Boulder, CO (United States); Bland, Geoff [National Aeronautics and Space Administration (NASA), Washington, DC (United States)

2017-03-01

The Evaluation of Routine Atmospheric Sounding Measurements using Unmanned Systems (ERASMUS) campaign was proposed with two central goals; to obtain scientifically relevant measurements of quantities related to clouds, aerosols, and radiation, including profiles of temperature, humidity, and aerosol particles, the structure of the arctic atmosphere during transitions between clear and cloudy states, measurements that would allow us to evaluate the performance of retrievals from U.S. Department of Energy (DOE) Atmospheric Radiation Measurement (ARM) Climate Research Facility remote sensors in the Arctic atmosphere, and information on the spatial variability of heat and moisture fluxes from the arctic surface; and to demonstrate unmanned aerial system (UAS) capabilities in obtaining measurements relevant to the ARM and ASR programs, particularly for improving our understanding of Arctic clouds and aerosols.

Development of a Ground-Based Atmospheric Monitoring Network for the Global Mercury Observation System (GMOS

Directory of Open Access Journals (Sweden)

Sprovieri F.

2013-04-01

Full Text Available Consistent, high-quality measurements of atmospheric mercury (Hg are necessary in order to better understand Hg emissions, transport, and deposition on a global scale. Although the number of atmospheric Hg monitoring stations has increased in recent years, the available measurement database is limited and there are many regions of the world where measurements have not been extensively performed. Long-term atmospheric Hg monitoring and additional ground-based monitoring sites are needed in order to generate datasets that will offer new insight and information about the global scale trends of atmospheric Hg emissions and deposition. In the framework of the Global Mercury Observation System (GMOS project, a coordinated global observational network for atmospheric Hg is being established. The overall research strategy of GMOS is to develop a state-of-the-art observation system able to provide information on the concentration of Hg species in ambient air and precipitation on the global scale. This network is being developed by integrating previously established ground-based atmospheric Hg monitoring stations with newly established GMOS sites that are located both at high altitude and sea level locations, as well as in climatically diverse regions. Through the collection of consistent, high-quality atmospheric Hg measurement data, we seek to create a comprehensive assessment of atmospheric Hg concentrations and their dependence on meteorology, long-range atmospheric transport and atmospheric emissions.

Atmospheric chemistry, sources and sinks of carbon suboxide, C3O2

Science.gov (United States)

Keßel, Stephan; Cabrera-Perez, David; Horowitz, Abraham; Veres, Patrick R.; Sander, Rolf; Taraborrelli, Domenico; Tucceri, Maria; Crowley, John N.; Pozzer, Andrea; Stönner, Christof; Vereecken, Luc; Lelieveld, Jos; Williams, Jonathan

2017-07-01

Carbon suboxide, O = C = C = C = O, has been detected in ambient air samples and has the potential to be a noxious pollutant and oxidant precursor; however, its lifetime and fate in the atmosphere are largely unknown. In this work, we collect an extensive set of studies on the atmospheric chemistry of C3O2. Rate coefficients for the reactions of C3O2 with OH radicals and ozone were determined as kOH = (2.6 ± 0.5) × 10-12 cm3 molecule-1 s-1 at 295 K (independent of pressure between ˜ 25 and 1000 mbar) and kO3 chemistry-general circulation model. The results indicate sub-pptv levels at the Earth's surface, up to about 10 pptv in regions with relatively strong sources, e.g. influenced by biomass burning, and a mean lifetime of ˜ 3.2 days. These predictions carry considerable uncertainty, as more measurement data are needed to determine ambient concentrations and constrain the source strengths.

On measuring surface wave phase velocity from station–station cross-correlation of ambient signal

DEFF Research Database (Denmark)

Boschi, Lapo; Weemstra, Cornelis; Verbeke, Julie

2012-01-01

We apply two different algorithms to measure surface wave phase velocity, as a function of frequency, from seismic ambient noise recorded at pairs of stations from a large European network. The two methods are based on consistent theoretical formulations, but differ in the implementation: one met...

Measurement of the Residual Gases O2 and CO2 in Meat Products Packed in Modified Atmosphere

Directory of Open Access Journals (Sweden)

Jozef Čapla

2013-02-01

Full Text Available Nowadays, consumers have increased demand for quality and food safety and also rising demand for natural foods without chemical additives. There are many ways to presserve freshness of these products, one of them is modified atmosphere packaging, which can mean elimination and/or replacement surrounding the product before closing it in package with a mixture of gases other than the original ambient air atmosphere. for replacement of atmosphere are generally used three types of gases such as carbon dioxide, oxygen and nitrogen. this type of packaging is often used for meat and meat products, which belongs to foods that are under normal conditions perishable and for increasing the shelf life of meat products are also used various other preservation methods or their combinations. Packaging of meat and meat products in modified atmosphere is usually made with a high content of carbon dioxide, which has good bacteriostatic and fungistatic effect and is also an effective mean for increasing the shelf life of packaged products during storage and sale.

Ambient Space and Ambient Sensation

DEFF Research Database (Denmark)

Schmidt, Ulrik

The ambient is the aesthetic production of the sensation of being surrounded. As a concept, 'ambient' is mostly used in relation to the music genre 'ambient music' and Brian Eno's idea of environmental background music. However, the production of ambient sensations must be regarded as a central...... aspect of the aesthetization of modern culture in general, from architecture, transport and urbanized lifeforms to film, sound art, installation art and digital environments. This presentation will discuss the key aspects of ambient aesthetization, including issues such as objectlessness...

ambient volatile organic compounds pollution and ozone formation

African Journals Online (AJOL)

OLUMAYEDE

2013-08-01

Aug 1, 2013 ... Volatile organic compound (VOC) species react at different rate and exhibit differences in reactivity with respect to ozone formation in polluted urban atmosphere. To assess this, the variations pattern, reactivity relative to OH radical and ozone creation potential of ambient VOCs were investigated in field.

Environmentally Persistent Free Radical (EPFRs) - Ambient Air Particulates, Soils and Fate of Some Pollutants

Science.gov (United States)

Lomnicki, S. M.

2017-12-01

Environmentally Persistent Free Radicals (EPFRs) are relatively recently discovered species that are present on ambient air particulates. Their origin is typically associated with the combustion borne PM, where in the cool zone of the combustion process aromatic precursors react with the metal centers of particulates forming surface-organic complex with radical characteristics. EPFRs have been found to be sufficiently resistant to be emitted from the combustion sources and persist in the ambient air on particulates. Their inhalation has been associated with severe health effects, and potentially are one of the major agents contributing the epidemiological risks of PM exposure. Interestingly, EPFRs can be formed not only at the elevated temperatures but also in ambient conditions, where the contact of precursor molecules with transition metal (but not only) domains can result in adsorbate complexes. In fact, EPFRs have been detected in the contaminated soils, or during the oil spill incidents. It is very likely, that the interaction of some molecules released to the air can result in the formation of EPFRs on the ambient air particulates in atmospheric conditions. These species can be a natural degradation by-products that lead to the formation of oxygenated organics in ambient atmosphere.

Soil microbes shift C-degrading activity along an ambient and experimental nitrogen gradient

Science.gov (United States)

Moore, J.; Frey, S. D.

2017-12-01

The balance between soil carbon (C) accumulation and decomposition is determined in large part by the activity and biomass of soil microbes, and yet their sensitivity to global changes remains unresolved. Atmospheric nitrogen (N) deposition has increased 22% (for NH4+) in the last two decades despite initiation of the Clean Air Act. Nitrogen deposition alters ecosystem processes by changing nutrient availability and soil pH, creating physiologically stressful environments that select for stress tolerant microbes. The functional fungal community may switch from domination by species with traits associated with decomposition via oxidative enzymes to traits associated with stress tolerance if global changes push fungal physiological limits. We examined changes in soil microbial activity across seven sites representing a gradient of ambient atmospheric N deposition, and five of these sites also had long-term N addition experiments. We measured changes in abundance of decomposition genes and C mineralization rates as indicators of microbial activity. We expected microbes to be less active with high N deposition, thus decreasing C mineralization rates. We found that C mineralization rates declined with total N deposition (ambient plus experimental additions), and this decline was more sensitive to N deposition where it occurred naturally compared to experimental treatments. Carbon mineralization declined by 3% in experimentally fertilized soils compared to 10% in control soils for every 1 kg/ha/y increase in ambient N deposition. Thus, microbes exposed to ambient levels of N deposition (2 - 12 kg/ha/y) had a stronger response than those exposed to fertilized soils (20 - 50 kg/ha/y). Long-term experimental N-addition seems to have selected for a microbial community that is tolerant of high N deposition. In sum, we provide evidence that soil microbial activity responded to N deposition, and may shift over time to a community capable of tolerating environmental change.

Unrestricted release measurements with ambient air ionization monitors

International Nuclear Information System (INIS)

MacArthur, D.; Gunn, R.; Dockray, T.; Luff, C.

1999-01-01

Radiation monitoring systems based on the long-range alpha detection (LRAD) technique, such as the BNFL Instruments IonSens trademark, provide a single contamination measurement for an entire object rather than the more familiar individual readings for smaller surface areas. The LRAD technique relies on the ionization of ambient air molecules by alpha particles, and the subsequent detection of these ions, rather than direct detection of the alpha particles themselves. A single monitor can detect all of the ions produced over a large object and report a total contamination level for the entire surface of that object. However, both the unrestricted release limits specified in USDOE Order 5400.5 (and similar documents in other countries), and the definitions of radioactive waste categories, are stated in terms of contamination per area. Thus, conversion is required between the total effective contamination as measured by the LRAD-based detector and the allowable release limits. In addition, since the release limits were not written assuming an averaging detector system, the method chosen to average the assumed contamination over the object can have a significant impact on the effective sensitivity of the detector

Metrological challenges for measurements of key climatological observables: oceanic salinity and pH, and atmospheric humidity. Part 1: overview

Science.gov (United States)

Feistel, R.; Wielgosz, R.; Bell, S. A.; Camões, M. F.; Cooper, J. R.; Dexter, P.; Dickson, A. G.; Fisicaro, P.; Harvey, A. H.; Heinonen, M.; Hellmuth, O.; Kretzschmar, H.-J.; Lovell-Smith, J. W.; McDougall, T. J.; Pawlowicz, R.; Ridout, P.; Seitz, S.; Spitzer, P.; Stoica, D.; Wolf, H.

2016-02-01

Water in its three ambient phases plays the central thermodynamic role in the terrestrial climate system. Clouds control Earth’s radiation balance, atmospheric water vapour is the strongest ‘greenhouse’ gas, and non-equilibrium relative humidity at the air-sea interface drives evaporation and latent heat export from the ocean. On climatic time scales, melting ice caps and regional deviations of the hydrological cycle result in changes of seawater salinity, which in turn may modify the global circulation of the oceans and their ability to store heat and to buffer anthropogenically produced carbon dioxide. In this paper, together with three companion articles, we examine the climatologically relevant quantities ocean salinity, seawater pH and atmospheric relative humidity, noting fundamental deficiencies in the definitions of those key observables, and their lack of secure foundation on the International System of Units, the SI. The metrological histories of those three quantities are reviewed, problems with their current definitions and measurement practices are analysed, and options for future improvements are discussed in conjunction with the recent seawater standard TEOS-10. It is concluded that the International Bureau of Weights and Measures, BIPM, in cooperation with the International Association for the Properties of Water and Steam, IAPWS, along with other international organizations and institutions, can make significant contributions by developing and recommending state-of-the-art solutions for these long standing metrological problems in climatology.

"Atmospheric Radiation Measurement (ARM) Research Facility at Oliktok Point Alaska"

Science.gov (United States)

Helsel, F.; Ivey, M.; Hardesty, J.; Roesler, E. L.; Dexheimer, D.

2017-12-01

Scientific Infrastructure To Support Atmospheric Science, Aerosol Science and UAS's for The Department Of Energy's Atmospheric Radiation Measurement Programs At The Mobile Facility 3 Located At Oliktok Point, Alaska.The Atmospheric Radiation Measurement (ARM) Program's Mobile Facility 3 (AMF3) located at Oliktok Point, Alaska is a U.S. Department of Energy (DOE) site designed to collect data and help determine the impact that clouds and aerosols have on solar radiation. AMF3 provides a scientific infrastructure to support instruments and collect arctic data for the international arctic research community. The infrastructure at AMF3/Oliktok is designed to be mobile and it may be relocated in the future to support other ARM science missions. AMF3's present base line instruments include: scanning precipitation Radars, cloud Radar, Raman Lidar, Eddy correlation flux systems, Ceilometer, Balloon sounding system, Atmospheric Emitted Radiance Interferometer (AERI), Micro-pulse Lidar (MPL) Along with all the standard metrological measurements. In addition AMF3 provides aerosol measurements with a Mobile Aerosol Observing System (MAOS). Ground support for Unmanned Aerial Systems (UAS) and tethered balloon flights. Data from these instruments and systems are placed in the ARM data archives and are available to the international research community. This poster will discuss what instruments and systems are at the ARM Research Facility at Oliktok Point Alaska.

Measuring Atmospheric Abundances and Rotation of a Brown Dwarf with a Measured Mass and Radius

Science.gov (United States)

Birkby, Jayne

2015-08-01

There are no cool brown dwarfs with both a well-characterized atmosphere and a measured mass and radius. LHS 6343, a brown dwarf transiting one member of an M+M binary in the Kepler field, provides the first opportunity to tie theoretical atmospheric models to the observed brown dwarf mass-radius diagram. We propose four half-nights of observations with NIRSPAO in 2015B to measure spectral features in LHS 6343 C by detecting the relative motions of absorption features during the system's orbit. In addition to abundances, we will directly measure the brown dwarf's projected rotational velocity and mass.

Atmospheric effect on the ground-based measurements of broadband surface albedo

Directory of Open Access Journals (Sweden)

T. Manninen

2012-11-01

Full Text Available Ground-based pyranometer measurements of the (clear-sky broadband surface albedo are affected by the atmospheric conditions (mainly by aerosol particles, water vapour and ozone. A new semi-empirical method for estimating the magnitude of the effect of atmospheric conditions on surface albedo measurements in clear-sky conditions is presented. Global and reflected radiation and/or aerosol optical depth (AOD at two wavelengths are needed to apply the method. Depending on the aerosol optical depth and the solar zenith angle values, the effect can be as large as 20%. For the cases we tested using data from the Cabauw atmospheric test site in the Netherlands, the atmosphere caused typically up to 5% overestimation of surface albedo with respect to corresponding black-sky surface albedo values.

Optimal interpolation method for intercomparison of atmospheric measurements.

Science.gov (United States)

Ridolfi, Marco; Ceccherini, Simone; Carli, Bruno

2006-04-01

Intercomparison of atmospheric measurements is often a difficult task because of the different spatial response functions of the experiments considered. We propose a new method for comparison of two atmospheric profiles characterized by averaging kernels with different vertical resolutions. The method minimizes the smoothing error induced by the differences in the averaging kernels by exploiting an optimal interpolation rule to map one profile into the retrieval grid of the other. Compared with the techniques published so far, this method permits one to retain the vertical resolution of the less-resolved profile involved in the intercomparison.

Novel Measurements of Aerosol Particle Interfaces Using Biphasic Microfluidics

Science.gov (United States)

Metcalf, A. R.; Dutcher, C. S.

2014-12-01

Secondary organic aerosol (SOA) particles are nearly ubiquitous in the atmosphere and yet there remains large uncertainties in their formation processes and ambient properties. These particles are complex microenvironments, which can contain multiple interfaces due to internal aqueous-organic phase partitioning and to the external liquid-vapor surface. These aerosol interfaces can profoundly affect the fate of condensable organic compounds emitted into the atmosphere by altering the way in which organic vapors interact with the ambient aerosol. Aerosol interfaces affect particle internal structure, species uptake, equilibrium partitioning, activation to cloud condensation or ice nuclei, and optical properties. For example, organic thin films can shield the core of the aerosol from the ambient environment, which may disrupt equilibrium partitioning and mass transfer. To improve our ability to accurately predict the fate of SOA in the atmosphere, we must improve our knowledge of aerosol interfaces and their interactions with the ambient environment. Few technologies exist to accurately probe aerosol interfaces at atmospherically-relevant conditions. In this talk, a novel method using biphasic microscale flows will be introduced for generating, trapping, and perturbing complex interfaces at atmospherically relevant conditions. These microfluidic experiments utilize high-speed imaging to monitor interfacial phenomena at the microscale and are performed with phase contrast and fluorescence microscopy on a temperature-controlled inverted microscope stage. From these experiments, interfacial thermodynamic properties such as surface tension, rheological properties such as interfacial moduli, and kinetic properties such as mass transfer coefficients can be measured or inferred. Chemical compositions of the liquid phases studied here span a range of viscosities and include electrolyte and water soluble organic acid species often observed in the atmosphere, such as mixtures

Influences on the fraction of hydrophobic and hydrophilic black carbon in the atmosphere

Directory of Open Access Journals (Sweden)

G. R. McMeeking

2011-05-01

Full Text Available Black carbon (BC is a short term climate forcer that directly warms the atmosphere, slows convection, and hinders quantification of the effect of greenhouse gases on climate change. The atmospheric lifetime of BC particles with respect to nucleation scavenging in clouds is controlled by their ability to serve as cloud condensation nuclei (CCN. To serve as CCN under typical conditions, hydrophobic BC particles must acquire hygroscopic coatings. However, the quantitative relationship between coatings and hygroscopic properties for ambient BC particles is not known nor is the time scale for hydrophobic-to-hydrophilic conversion. Here we introduce a method for measuring the hygroscopicity of externally and internally mixed BC particles by coupling a single particle soot photometer with a humidified tandem differential mobility analyzer. We test this technique using uncoated and coated laboratory generated model BC compounds and apply it to characterize the hygroscopicity distribution of ambient BC particles. From these data we derive that the observed number fraction of BC that is CCN active at 0.2 % supersaturation is generally low in an urban area near sources and that it varies with the trajectory of the airmass. We anticipate that our method can be combined with measures of air parcel physical and photochemical age to provide the first quantitative estimates for characterizing hydrophobic-to-hydrophilic conversion rates in the atmosphere.

A spectroscopic transfer standard for accurate atmospheric CO measurements

Science.gov (United States)

Nwaboh, Javis A.; Li, Gang; Serdyukov, Anton; Werhahn, Olav; Ebert, Volker

2016-04-01

Atmospheric carbon monoxide (CO) is a precursor of essential climate variables and has an indirect effect for enhancing global warming. Accurate and reliable measurements of atmospheric CO concentration are becoming indispensable. WMO-GAW reports states a compatibility goal of ±2 ppb for atmospheric CO concentration measurements. Therefore, the EMRP-HIGHGAS (European metrology research program - high-impact greenhouse gases) project aims at developing spectroscopic transfer standards for CO concentration measurements to meet this goal. A spectroscopic transfer standard would provide results that are directly traceable to the SI, can be very useful for calibration of devices operating in the field, and could complement classical gas standards in the field where calibration gas mixtures in bottles often are not accurate, available or stable enough [1][2]. Here, we present our new direct tunable diode laser absorption spectroscopy (dTDLAS) sensor capable of performing absolute ("calibration free") CO concentration measurements, and being operated as a spectroscopic transfer standard. To achieve the compatibility goal stated by WMO for CO concentration measurements and ensure the traceability of the final concentration results, traceable spectral line data especially line intensities with appropriate uncertainties are needed. Therefore, we utilize our new high-resolution Fourier-transform infrared (FTIR) spectroscopy CO line data for the 2-0 band, with significantly reduced uncertainties, for the dTDLAS data evaluation. Further, we demonstrate the capability of our sensor for atmospheric CO measurements, discuss uncertainty calculation following the guide to the expression of uncertainty in measurement (GUM) principles and show that CO concentrations derived using the sensor, based on the TILSAM (traceable infrared laser spectroscopic amount fraction measurement) method, are in excellent agreement with gravimetric values. Acknowledgement Parts of this work have been

Comments on the water cycle of the atmosphere and its measurement

International Nuclear Information System (INIS)

Benton, G.S.

1967-01-01

There are two major water cycles of the atmosphere: the meridional cycle, which results in a latitudinal exchange of water, and the hydrological cycle, which carries water from the oceans over the continents. In the present paper a model is used for the estimation of atmospheric water balance from direct measurements of atmospheric vapour flux and limitation of this model are discussed

Secondary organic aerosol formation from ambient air in an oxidation flow reactor in central Amazonia

Science.gov (United States)

Palm, Brett B.; de Sá, Suzane S.; Day, Douglas A.; Campuzano-Jost, Pedro; Hu, Weiwei; Seco, Roger; Sjostedt, Steven J.; Park, Jeong-Hoo; Guenther, Alex B.; Kim, Saewung; Brito, Joel; Wurm, Florian; Artaxo, Paulo; Thalman, Ryan; Wang, Jian; Yee, Lindsay D.; Wernis, Rebecca; Isaacman-VanWertz, Gabriel; Goldstein, Allen H.; Liu, Yingjun; Springston, Stephen R.; Souza, Rodrigo; Newburn, Matt K.; Lizabeth Alexander, M.; Martin, Scot T.; Jimenez, Jose L.

2018-01-01

Secondary organic aerosol (SOA) formation from ambient air was studied using an oxidation flow reactor (OFR) coupled to an aerosol mass spectrometer (AMS) during both the wet and dry seasons at the Observations and Modeling of the Green Ocean Amazon (GoAmazon2014/5) field campaign. Measurements were made at two sites downwind of the city of Manaus, Brazil. Ambient air was oxidized in the OFR using variable concentrations of either OH or O3, over ranges from hours to days (O3) or weeks (OH) of equivalent atmospheric aging. The amount of SOA formed in the OFR ranged from 0 to as much as 10 µg m-3, depending on the amount of SOA precursor gases in ambient air. Typically, more SOA was formed during nighttime than daytime, and more from OH than from O3 oxidation. SOA yields of individual organic precursors under OFR conditions were measured by standard addition into ambient air and were confirmed to be consistent with published environmental chamber-derived SOA yields. Positive matrix factorization of organic aerosol (OA) after OH oxidation showed formation of typical oxidized OA factors and a loss of primary OA factors as OH aging increased. After OH oxidation in the OFR, the hygroscopicity of the OA increased with increasing elemental O : C up to O : C ˜ 1.0, and then decreased as O : C increased further. Possible reasons for this decrease are discussed. The measured SOA formation was compared to the amount predicted from the concentrations of measured ambient SOA precursors and their SOA yields. While measured ambient precursors were sufficient to explain the amount of SOA formed from O3, they could only explain 10-50 % of the SOA formed from OH. This is consistent with previous OFR studies, which showed that typically unmeasured semivolatile and intermediate volatility gases (that tend to lack C = C bonds) are present in ambient air and can explain such additional SOA formation. To investigate the sources of the unmeasured SOA-forming gases during this campaign

Mars Atmospheric Entry Integrated Navigation with Partial Intermittent Measurements

Directory of Open Access Journals (Sweden)

Tai-shan Lou

2017-01-01

Full Text Available Signal degradation suffered by the vehicle is a combination brownout and blackout during Mars atmospheric entry. The communications brownout means that signal fades and blackout means that the signal is lost completely. The communications brownout and blackout periods are analyzed and predicted with an altitude and velocity profiles. In the brownout period, the range measurements between the vehicle and the orbiters are modeled as intermittent measurements with the radio signal arrival probabilities, which are distributed as a Rayleigh distribution of the electron number density around the entry vehicle. A new integrated navigation strategy during the Mars atmospheric entry phase is proposed to consider the probabilities of the radio measurements in the communications brownout and blackout periods under the IMU/beacon scenario based on the information filter with intermittent measurements. Numerical navigation simulations are designed to show the performance of the proposed navigation strategy under the integrated navigation scenario.

Measurement of atmospheric pollutants

Energy Technology Data Exchange (ETDEWEB)

1975-01-01

Studies of simplified methods of determining various atmospheric pollutants were performed. Measurements with Kitagawa detecting tubes were made in front of Shibuya Station in Tokyo on October 27, 1973. The number of cars that passed the site was counted then the nitrogen dioxide, sulfur dioxide, hydrocarbons and carbon monoxide content was determined. The number of cars was about 7000-12,000 between 9 AM and 6 PM. The heaviest traffic occurred around 10 am, and the least traffic occurred around 1 pm. A simulation experiment of smoking was also performed. A simplified model of smoking indicated that the concentration of CO in the mouth is as high as 10,000-15,000 ppM. The simplified measurement of sulfur dioxide and nitrogen dioxide by the use of a small piece of an alkaline filter was also investigated. A photoelectric colorimeter gave an excellent demonstration of the pollution due to SO/sub 2/ and NO/sub 2/. A simplified determination of NO/sub 2/ by the Saltzman method was also performed.

In Situ Measurement of Atmospheric Krypton and Xenon on Mars with Mars Science Laboratory

Science.gov (United States)

Conrad, P. G.; Malespin, C. A.; Franz, H. B.; Pepin, R. O.; Trainer, M. G.; Schwenzer, S. P.; Atreya, S. K.; Freissinet, C.; Jones, J. H.; Manning, H.;

Historical Ambient Air Quality Data Inventory

Data.gov (United States)

U.S. Environmental Protection Agency — The Historical Ambient Air Quality Data Inventory contains measured and estimated data on ambient air pollution for use in assessing air quality, assisting in...

On the permanent hip-stabilizing effect of atmospheric pressure.

Science.gov (United States)

Prietzel, Torsten; Hammer, Niels; Schleifenbaum, Stefan; Kaßebaum, Eric; Farag, Mohamed; von Salis-Soglio, Georg

2014-08-22

Hip joint dislocations related to total hip arthroplasty (THA) are a common complication especially in the early postoperative course. The surgical approach, the alignment of the prosthetic components, the range of motion and the muscle tone are known factors influencing the risk of dislocation. A further factor that is discussed until today is atmospheric pressure which is not taken into account in the present THA concepts. The aim of this study was to investigate the impact of atmospheric pressure on hip joint stability. Five joint models (Ø 28-44 mm), consisting of THA components were hermetically sealed with a rubber capsule, filled with a defined amount of fluid and exposed to varying ambient pressure. Displacement and pressure sensors were used to record the extent of dislocation related to intraarticular and ambient pressure. In 200 experiments spontaneous dislocations of the different sized joint models were reliably observed once the ambient pressure was lower than 6.0 kPa. Increasing the ambient pressure above 6.0 kPa immediately and persistently reduced the joint models until the ambient pressure was lowered again. Displacement always exceeded half the diameter of the joint model and was independent of gravity effects. This experimental study gives strong evidence that the hip joint is permanently stabilized by atmospheric pressure, confirming the theories of Weber and Weber (1836). On basis of these findings the use of larger prosthetic heads, capsular repair and the deployment of an intracapsular Redon drain are proposed to substantially decrease the risk of dislocation after THA. Copyright © 2014 Elsevier Ltd. All rights reserved.

Measurement of atmospheric MTF in a littoral environment

CSIR Research Space (South Africa)

Griffith, DJ

2008-09-01

Full Text Available Measurement of atmospheric modulation transfer function (MTF) derived from the point spread function is an alternative to the use of scintillometry in characterizing the effects of turbulence as well as optical scattering. This experiment involved...

Measuring the greenhouse effect and radiative forcing through the atmosphere

Science.gov (United States)

Philipona, Rolf; Kräuchi, Andreas; Brocard, Emmanuel

2013-04-01

In spite of a large body of existing measurements of incoming shortwave solar radiation and outgoing longwave terrestrial radiation at the Earth's surface and at the top of the atmosphere, there are few observations documenting how radiation profiles change through the atmosphere - information that is necessary to fully quantify the greenhouse effect of the Earth's atmosphere. Using weather balloons and specific radiometer equipped radiosondes, we continuously measured shortwave and longwave radiation fluxes from the surface of the Earth up to altitudes of 35 kilometers in the upper stratosphere. Comparing radiation profiles from night measurements with different amounts of water vapor, we show evidence of large greenhouse forcing. We show, that under cloud free conditions, water vapor increases with Clausius-Clapeyron ( 7% / K), and longwave downward radiation at the surface increases by 8 Watts per square meter per Kelvin. The longwave net radiation however, shows a positive increase (downward) of 2.4 Watts per square meter and Kelvin at the surface, which decreases with height and shows a similar but negative increase (upward) at the tropopause. Hence, increased tropospheric water vapor increases longwave net radiation towards the ground and towards space, and produces a heating of 0.42 Kelvin per Watt per square meter at the surface. References: Philipona et al., 2012: Solar and thermal radiation profiles and radiative forcing measured through the atmosphere. Geophys. Res. Lett., 39, L13806, doi: 10.1029/2012GL052087.

Atmospheric mixing ratios of methyl ethyl ketone (2-butanone in tropical, boreal, temperate and marine environments

Directory of Open Access Journals (Sweden)

A. M. Yáñez-Serrano

2016-09-01

Full Text Available Methyl ethyl ketone (MEK enters the atmosphere following direct emission from vegetation and anthropogenic activities, as well as being produced by the gas-phase oxidation of volatile organic compounds (VOCs such as n-butane. This study presents the first overview of ambient MEK measurements at six different locations, characteristic of forested, urban and marine environments. In order to understand better the occurrence and behaviour of MEK in the atmosphere, we analyse diel cycles of MEK mixing ratios, vertical profiles, ecosystem flux data, and HYSPLIT back trajectories, and compare with co-measured VOCs. MEK measurements were primarily conducted with proton-transfer-reaction mass spectrometer (PTR-MS instruments. Results from the sites under biogenic influence demonstrate that vegetation is an important source of MEK. The diel cycle of MEK follows that of ambient temperature and the forest structure plays an important role in air mixing. At such sites, a high correlation of MEK with acetone was observed (e.g. r2 = 0.96 for the SMEAR Estonia site in a remote hemiboreal forest in Tartumaa, Estonia, and r2 = 0.89 at the ATTO pristine tropical rainforest site in central Amazonia. Under polluted conditions, we observed strongly enhanced MEK mixing ratios. Overall, the MEK mixing ratios and flux data presented here indicate that both biogenic and anthropogenic sources contribute to its occurrence in the global atmosphere.

Compact high-resolution echelle-AOTF NIR spectrometer for atmospheric measurements

Science.gov (United States)

Korablev, Oleg I.; Bertaux, Jean-Loup; Vinogradov, Imant I.; Kalinnikov, Yurii K.; Nevejans, D.; Neefs, E.; Le Barbu, T.; Durry, G.

2017-11-01

A new concept of a high-resolution near-IR spectrometer consisting of an echelle grating combined with an acousto-optic tunable filter (AOTF) for separation of diffraction orders, is developed for space-borne studies of planetary atmospheres. A compact design with no moving parts within the mass budget of 3-5 kg allows to reach the resolving power λ/Δλ of 20000-30000. Only a small piece of spectrum in high diffraction orders can be measured at a time, but thanks to flexibility of the AOTF electrical tuning, such pieces of spectrum can be measured randomly and rapidly within the spectral range. This development can be used for accurate measurements of important atmospheric gases, such as CO2 in terrestrial atmosphere, isotopic ratios and minor gases. A spectrometer, based on this principle, SOIR (Solar Occultation InfraRed) is being built for Venus Express (2005) ESA mission. Instruments based on this principle have high potential for the studies of the Earth, in particular for measurements of isotopes of water in the lower atmosphere, either in solar occultation profiling (tangent altitude <10 km), or observing solar glint for integral quantities of the components. Small size of hardware makes them ideal for micro-satellites, which are now agile enough to provide necessary pointing for solar occultation or glint observations. Also, the atmosphere of Mars has never been observed at local scales with such a high spectral resolution. A laboratory prototype consisting of 275-mm echelle spectrometer with Hamamatsu InGaAs 512-pixel linear array and the AOTF has demonstrated λ/Δλ≍30000 in the spectral range of 1-1.7 μm. The next set up, covering the spectral ranges of 1-1.7 μm and 2.3-4.3 μm, and the Venus Express SOIR are briefly discussed.

Tomographic reconstruction of atmospheric volumes from infrared limb-imager measurements

Energy Technology Data Exchange (ETDEWEB)

Ungermann, Joern

2011-08-12

State-of-the art nadir and limb-sounders, but also in situ measurements, do not offer the capability to highly resolve the atmosphere in all three dimensions. This leaves an observational gap with respect to small-scale structures that arise frequently in the atmosphere and that still lack a quantitative understanding. For instance, filaments and tropopause folds in the upper troposphere and lower stratosphere (UTLS) are crucial for its composition and variability. One way to achieve a highly resolved three-dimensional (3-D) picture of the atmosphere is the tomographic evaluation of limb-imager measurements. This thesis presents a methodology for the tomographic reconstruction of atmospheric constituents. To be able to deal with the large increase of observations and unknowns compared to conventional retrievals, great care is taken to reduce memory consumption and processing time. This method is used to evaluate the performance of two upcoming infrared limb-imager instruments and to prepare their missions. The first examined instrument is the infrared limb-imager on board of PREMIER (Process Exploration through Measurements of Infrared and millimetrewave Emitted Radiation), one of three remaining candidates for ESA's 7th Earth Explorer mission. Scientific goals of PREMIER are, among others, the examination of gravity waves and the quantification of processes controlling atmospheric composition in the UTLS, a region of particular importance for climate change. Simulations based on the performance requirements of this instrument deliver a vertical resolution that is slightly better than its vertical field-of-view (about 0.75 km) and a horizontal resolution of {approx}25km x 70 km. Non-linear end-to-end simulations for various gravity wave patterns demonstrate that the high 3-D resolution of PREMIER considerably extends the range of detectable gravity waves in terms of horizontal and vertical wavelength compared to previous observations. The second examined

Tomographic reconstruction of atmospheric volumes from infrared limb-imager measurements

Energy Technology Data Exchange (ETDEWEB)

Ungermann, Joern

2011-08-12

State-of-the art nadir and limb-sounders, but also in situ measurements, do not offer the capability to highly resolve the atmosphere in all three dimensions. This leaves an observational gap with respect to small-scale structures that arise frequently in the atmosphere and that still lack a quantitative understanding. For instance, filaments and tropopause folds in the upper troposphere and lower stratosphere (UTLS) are crucial for its composition and variability. One way to achieve a highly resolved three-dimensional (3-D) picture of the atmosphere is the tomographic evaluation of limb-imager measurements. This thesis presents a methodology for the tomographic reconstruction of atmospheric constituents. To be able to deal with the large increase of observations and unknowns compared to conventional retrievals, great care is taken to reduce memory consumption and processing time. This method is used to evaluate the performance of two upcoming infrared limb-imager instruments and to prepare their missions. The first examined instrument is the infrared limb-imager on board of PREMIER (Process Exploration through Measurements of Infrared and millimetrewave Emitted Radiation), one of three remaining candidates for ESA's 7th Earth Explorer mission. Scientific goals of PREMIER are, among others, the examination of gravity waves and the quantification of processes controlling atmospheric composition in the UTLS, a region of particular importance for climate change. Simulations based on the performance requirements of this instrument deliver a vertical resolution that is slightly better than its vertical field-of-view (about 0.75 km) and a horizontal resolution of {approx}25km x 70 km. Non-linear end-to-end simulations for various gravity wave patterns demonstrate that the high 3-D resolution of PREMIER considerably extends the range of detectable gravity waves in terms of horizontal and vertical wavelength compared to previous observations. The second examined instrument

Conversion of an Alpha CAM Monitor of Victoreen calibrated of factory for plutonium in a measurement monitor of radon in the atmosphere

International Nuclear Information System (INIS)

Moreno y Moreno, A.

2004-01-01

It is presented in this work the conversion of a monitor ALPHA CAM of the monitor Victoreen gauged of it manufactures for plutonium in a monitor for radon mensuration in the atmosphere. Those units in that the radon measures are expressed are: peak curies/unit of volume of air to sampling. This way one has to gauge and to supplement the software and the parts that the old one monitor for plutonium. It requires. This task implies: a) To calibrate and to determine the efficiency of the detector of accustomed to state of 1700 mm 2 for alpha particles coming from the radioactive series of the radon. b) to connect in series and to calibrate a flow measurer of air in it lines with the detector. Measures are presented of the ambient air and other places of the the historical area of the city of Puebla obtained with the team Converted ALPHA-CAM. (Author)

The impact of ambient dose rate measuring network and precipitation radar system for detection of environmental radioactivity released by accident

International Nuclear Information System (INIS)

Bleher, M; Stoehlker, U.

2003-01-01

For the surveillance of environmental radioactivity, the German measuring network of BfS consists of more than 2000 stations where the ambient gamma dose rate is continuously measured. This network is a helpful tool to detect and localise enhanced environmental contamination from artificial radionuclides. The threshold for early warning is so low, that already an additional dose rate contribution of 0,07 μGy/h is detectable. However, this threshold is frequently exceeded due to precipitation events caused by washout of natural activity in air. Therefore, the precipitation radar system of the German Weather Service provides valuable information on the problem, whether the increase of the ambient dose rate is due to natural or man-made events. In case of an accidental release, the data of this radar system show small area precipitation events and potential local hot spots not detected by the measuring network. For the phase of cloud passage, the ambient dose rate measuring network provides a reliable database for the evaluation of the current situation and its further development. It is possible to compare measured data for dose rate with derived intervention levels for countermeasures like ''sheltering''. Thus, critical regions can be identified and it is possible to verify implemented countermeasures. During and after this phase of cloud passage the measured data of the monitoring network help to adapt the results of the national decision support systems PARK and RODOS. Therefore, it is necessary to derive the actual additional contribution to the ambient dose rate. Map representations of measured dose rate are rapidly available and helpful to optimise measurement strategies of mobile systems and collection strategies for samples of agricultural products. (orig.)

Chemical Thermodynamics of Aqueous Atmospheric Aerosols: Modeling and Microfluidic Measurements

Science.gov (United States)

Nandy, L.; Dutcher, C. S.

2017-12-01

Accurate predictions of gas-liquid-solid equilibrium phase partitioning of atmospheric aerosols by thermodynamic modeling and measurements is critical for determining particle composition and internal structure at conditions relevant to the atmosphere. Organic acids that originate from biomass burning, and direct biogenic emission make up a significant fraction of the organic mass in atmospheric aerosol particles. In addition, inorganic compounds like ammonium sulfate and sea salt also exist in atmospheric aerosols, that results in a mixture of single, double or triple charged ions, and non-dissociated and partially dissociated organic acids. Statistical mechanics based on a multilayer adsorption isotherm model can be applied to these complex aqueous environments for predictions of thermodynamic properties. In this work, thermodynamic analytic predictive models are developed for multicomponent aqueous solutions (consisting of partially dissociating organic and inorganic acids, fully dissociating symmetric and asymmetric electrolytes, and neutral organic compounds) over the entire relative humidity range, that represent a significant advancement towards a fully predictive model. The model is also developed at varied temperatures for electrolytes and organic compounds the data for which are available at different temperatures. In addition to the modeling approach, water loss of multicomponent aerosol particles is measured by microfluidic experiments to parameterize and validate the model. In the experimental microfluidic measurements, atmospheric aerosol droplet chemical mimics (organic acids and secondary organic aerosol (SOA) samples) are generated in microfluidic channels and stored and imaged in passive traps until dehydration to study the influence of relative humidity and water loss on phase behavior.

Airborne Lidar Measurements of Atmospheric Pressure Made Using the Oxygen A-Band

Science.gov (United States)

Riris, Haris; Rodriquez, Michael D.; Allan, Graham R.; Hasselbrack, William E.; Mao, Jianping; Stephen, Mark A.; Abshire, James B.

2012-01-01

Accurate measurements of greenhouse gas mixing ratios on a global scale are currently needed to gain a better understanding of climate change and its possible impact on our planet. In order to remotely measure greenhouse gas concentrations in the atmosphere with regard to dry air, the air number density in the atmosphere is also needed in deriving the greenhouse gas concentrations. Since oxygen is stable and uniformly mixed in the atmosphere at 20.95%, the measurement of an oxygen absorption in the atmosphere can be used to infer the dry air density and used to calculate the dry air mixing ratio of a greenhouse gas, such as carbon dioxide or methane. OUT technique of measuring Oxygen uses integrated path differential absorption (IPDA) with an Erbium Doped Fiber Amplifier (EDF A) laser system and single photon counting module (SPCM). It measures the absorbance of several on- and off-line wavelengths tuned to an O2 absorption line in the A-band at 764.7 nm. The choice of wavelengths allows us to maximize the pressure sensitivity using the trough between two absorptions in the Oxygen A-band. Our retrieval algorithm uses ancillary meteorological and aircraft altitude information to fit the experimentally obtained lidar O2 line shapes to a model atmosphere and derives the pressure from the profiles of the two lines. We have demonstrated O2 measurements from the ground and from an airborne platform. In this paper we will report on our airborne measurements during our 2011 campaign for the ASCENDS program.

Radiation dosemeters and ambient dose rate measuring systems

International Nuclear Information System (INIS)

Maushart, R.

1985-01-01

The manufacturers have got the feeling that the PTB only reluctantly accepts complex dosimetric systems or systems with modern digital and microprocessor technology. Especially the fact that the PTB demands a restriction to a defined system configuration which must not be changed after design approval is felt to be a severe handicap. The rigid frame of design qualification forces manufacturers to adopt a two-tier development line, at least for ambient dose rate measuring systems, and frequently it is not necessarily the 'nature' system, i.e. equipment with modern technology, that is sent in to the PTB for testing. The way of solving the problem could be that PTB more readily accepts less familiar technologies, for instance by more frequently approving equipment at least preliminarily or for a restricted period of time, in order to collect experience. Another way could be to grant licence for system components, especially detectors. (orig./HP) [de

Atmospheric measurements of hydroperoxides and aldehydes during field campaigns : new results due to improvement of measurements techniques

Science.gov (United States)

François, S.; Sowka, I.; Poulain, L.; Monod, A.; Wortham, H.

2003-04-01

Hydroperoxides and aldehydes are considered as atmospheric reservoirs of OH, HO_2 and RO_2 radicals and can reflect the oxidizing levels of the atmosphere. They are considered as important gas phase photo-oxidants present in the atmosphere. However, the atmospheric role of these compounds can vary from one species to another, therefore it is essential to investigate their measurement and speciation in the atmosphere. Atmospheric measurements were realized during two different field campaigns in the Marseilles area (France). Hydroperoxides were trapped in aqueous phase, with a glass coil and analyzed by HPLC/fluorescence detector with post column derivatization. Aldehydes were trapped in a liquid phase containing 2-4 DNPH, with a mist chamber and analyzed by HPLC/UV. The analytical techniques provided individual separation and quantification of seven hydroperoxides (hydrogen peroxide, hydroxymethyl hydroperoxide, bis(hydroxymethyl) peroxide, 1-hydroxyethyl hydroperoxide, methyl hydroperoxide, ethyl hydroperoxide and peroxyacetic acid) and eleven volatile aldehydes (formaldehyde, acetaldehyde, acrolein, acetone, propionaldehyde, crotonaldehyde, butyraldehyde, benzaldehyde, glyoxal, valeraldehyde and methylglyoxal). The first field campaign was part of the ESCOMPTE project (June 4th to July 16th 2001). During this campaign five different sampling sites, at low altitudes (<= 285 m), were investigated (maritime, urban, sub-industrial, biogenic and rural sites) and atmospheric measurements were realized during photochemical air pollution events. The second field campaign was part of the BOND project (July 2nd to July 14th 2002). Atmospheric measurements of hydroperoxides were carried out on one biogenic site, at altitude 690 m. The measurement system was improved allowing online sampling and analysis. During these field campaigns collection efficiencies were better than 96% for hydroperoxides, and from 78% to 96% for aldehydes. Detection limits were between 7,3× 10-3 �

INSTRUMENTATION FOR MEASURING AND TRANSMISSION THE SOLAR RADIATION THROUGH EARTH’S ATMOSPHERE

Directory of Open Access Journals (Sweden)

Alexandru Dan Toma

2013-07-01

Full Text Available The Sun's energy is distributed over a broad range of the electromagnetic spectrum and Sun behaves approximately like a "blackbody" radiating at a temperature of about 5800 K with maximum output in the green-yellow part of the visible spectrum, around 500 nm. Not all solar radiation reaching the top of the atmosphere reaches Earth's surface due to a various optical phenomena in regard to solar radiation crossing the Earth’s atmosphere. In order to investigate them, there are two general categories of instruments used to measure the transmission of solar radiation through Earth's atmosphere: instruments that measure radiation from the entire sky and instruments that measure only direct solar radiation. Within each of these categories, instruments can be further subdivided into those that measure radiation over a broad range of wavelengths and those that measure only specific wavelengths.

Atmospheric Fluctuation Measurements with the Palomar Testbed Interferometer

Science.gov (United States)

Linfield, R. P.; Lane, B. F.; Colavita, M. M.; PTI Collaboration

Observations of bright stars with the Palomar Testbed Interferometer, at a wavelength of 2.2 microns, have been used to measure atmospheric delay fluctuations. The delay structure function Dτ(Δ t) was calculated for 66 scans (each >= 120s in length) on seven nights in 1997 and one in 1998. For all except one scan, Dτ exhibited a clean power law shape over the time interval 50-500 msec. Over shorter time intervals, the effect of the delay line servo loop corrupts Dτ. Over longer time intervals (usually starting at > 1s), the slope of Dτ decreases, presumably due to some combination of saturation e.g. finite turbulent layer thickness) and the effect of the finite wind speed crossing time on our 110 m baseline. The mean power law slopes for the eight nights ranged from 1.16 to 1.36, substantially flatter than the value of 1.67 for three dimensional Kolmogorov turbulence. Such sub-Kolmogorov slopes will result in atmospheric seeling (θ) that improves rapidly with increasing wavelength: θ propto λ1-(2β), where β is the observed power law slope of Dτ. The atmospheric errors in astrometric measurements with an interferometer will average down more quickly than in the Kolmogorov case.

The AquaVIT-1 intercomparison of atmospheric water vapor measurement techniques

Science.gov (United States)

Fahey, D. W.; Gao, R.-S.; Möhler, O.; Saathoff, H.; Schiller, C.; Ebert, V.; Krämer, M.; Peter, T.; Amarouche, N.; Avallone, L. M.; Bauer, R.; Bozóki, Z.; Christensen, L. E.; Davis, S. M.; Durry, G.; Dyroff, C.; Herman, R. L.; Hunsmann, S.; Khaykin, S. M.; Mackrodt, P.; Meyer, J.; Smith, J. B.; Spelten, N.; Troy, R. F.; Vömel, H.; Wagner, S.; Wienhold, F. G.

2014-09-01

The AquaVIT-1 intercomparison of atmospheric water vapor measurement techniques was conducted at the aerosol and cloud simulation chamber AIDA (Aerosol Interaction and Dynamics in the Atmosphere) at the Karlsruhe Institute of Technology, Germany, in October 2007. The overall objective was to intercompare state-of-the-art and prototype atmospheric hygrometers with each other and with independent humidity standards under controlled conditions. This activity was conducted as a blind intercomparison with coordination by selected referees. The effort was motivated by persistent discrepancies found in atmospheric measurements involving multiple instruments operating on research aircraft and balloon platforms, particularly in the upper troposphere and lower stratosphere, where water vapor reaches its lowest atmospheric values (less than 10 ppm). With the AIDA chamber volume of 84 m3, multiple instruments analyzed air with a common water vapor mixing ratio, by extracting air into instrument flow systems, by locating instruments inside the chamber, or by sampling the chamber volume optically. The intercomparison was successfully conducted over 10 days during which pressure, temperature, and mixing ratio were systematically varied (50 to 500 hPa, 185 to 243 K, and 0.3 to 152 ppm). In the absence of an accepted reference instrument, the absolute accuracy of the instruments was not established. To evaluate the intercomparison, the reference value was taken to be the ensemble mean of a core subset of the measurements. For these core instruments, the agreement between 10 and 150 ppm of water vapor is considered good with variation about the reference value of about ±10% (±1σ). In the region of most interest between 1 and 10 ppm, the core subset agreement is fair with variation about the reference value of ±20% (±1σ). The upper limit of precision was also derived for each instrument from the reported data. The implication for atmospheric measurements is that the

Atmospheric CO2 Concentration Measurements with Clouds from an Airborne Lidar

Science.gov (United States)

Mao, J.; Abshire, J. B.; Kawa, S. R.; Riris, H.; Allan, G. R.; Hasselbrack, W. E.; Numata, K.; Chen, J. R.; Sun, X.; DiGangi, J. P.; Choi, Y.

2017-12-01

Globally distributed atmospheric CO2 concentration measurements with high precision, low bias and full seasonal sampling are crucial to advance carbon cycle sciences. However, two thirds of the Earth's surface is typically covered by clouds, and passive remote sensing approaches from space are limited to cloud-free scenes. NASA Goddard is developing a pulsed, integrated-path differential absorption (IPDA) lidar approach to measure atmospheric column CO2 concentrations, XCO2, from space as a candidate for NASA's ASCENDS mission. Measurements of time-resolved laser backscatter profiles from the atmosphere also allow this technique to estimate XCO2 and range to cloud tops in addition to those to the ground with precise knowledge of the photon path-length. We demonstrate this measurement capability using airborne lidar measurements from summer 2017 ASCENDS airborne science campaign in Alaska. We show retrievals of XCO2 to ground and to a variety of cloud tops. We will also demonstrate how the partial column XCO2 to cloud tops and cloud slicing approach help resolving vertical and horizontal gradient of CO2 in cloudy conditions. The XCO2 retrievals from the lidar are validated against in situ measurements and compared to the Goddard Parameterized Chemistry Transport Model (PCTM) simulations. Adding this measurement capability to the future lidar mission for XCO2 will provide full global and seasonal data coverage and some information about vertical structure of CO2. This unique facility is expected to benefit atmospheric transport process studies, carbon data assimilation in models, and global and regional carbon flux estimation.

Radiation protection and ambient radioactivity monitoring in the area of the Asse mine. Annual report 1997

International Nuclear Information System (INIS)

Meyer, H.; Stippler, R.

1998-01-01

The number of annual sampling and measurements performed in compliance with the operator's monitoring duties have been the same as last year: 364. All measured radioactivity values were at the level of natural environmental radioactivity. Some samples and measurements reflected the fallout from former atmospheric nuclear weapons tests and the accident at the Chernobyl reactor. Personnel dosimetry was performed according to legal requirements of the Radiation Protection Ordinance, as were measurements for the monitoring of ambient doses, dose rates and radioactivity levels in the air of the mine structures. All measured values were below the maximum permissible personal doses and occupational dose limits. Ambient air measurements in the salt mine as in the preceding years detected low amounts of the nuclides H 3, C 14, Pb 210, and the short-lived daughter products of Rn 222 and Rn 220. The calculated radioactivity concentrations in the vicinity of the mine, derived from averaged annual effluents, to some part were below the average natural concentrations of the nuclides. The effluent-induced radiation dose at the most affected location was far below the limits set by the Radiation Protection Ordinance. (orig./CB) [de

A Study on intelligent measurement of nuclear explosion equivalent in atmosphere

International Nuclear Information System (INIS)

Wang Desheng; Wu Xiaohong

1999-01-01

Measurement of nuclear explosion equivalent in atmosphere is an important subject for nuclear survey. Based on the relations between nuclear explosion equivalent and the minimum illuminance time of light radiation from nuclear explosion. The method of RC differential valley time detection and mean-time taking is presented the method, using a single-chip computer as a intelligent part, can realize intelligent measurement of minimum illuminance time with high reliability and low power consumption. This method provides a practical mean for quick, accurate and reliable measurement of nuclear explosion equivalent in atmosphere

Atmospheric tritium. Measurement and application

International Nuclear Information System (INIS)

Frejaville, Gerard

1967-02-01

The possible origins of atmospheric tritium are reviewed and discussed. A description is given of enrichment (electrolysis and thermal diffusion) and counting (gas counters and liquid scintillation counters) processes which can be used for determining atmospheric tritium concentrations. A series of examples illustrates the use of atmospheric tritium for resolving a certain number of hydrological and glaciological problems. (author) [fr

Highly resolved measurements of atmospheric turbulence with the new 2d-Atmospheric Laser Cantilever Anemometer

International Nuclear Information System (INIS)

Jeromin, A; Schaffarczyk, A P; Puczylowski, J; Peinke, J; Hölling, M

2014-01-01

For the investigation of atmospheric turbulent flows on small scales a new anemometer was developed, the so-called 2d-Atmospheric Laser Cantilever Anemometer (2d-ALCA). It performs highly resolved measurements with a spatial resolution in millimeter range and temporal resolution in kHz range, thus detecting very small turbulent structures. The anemometer is a redesign of the successfully operating 2d-LCA for laboratory application. The new device was designed to withstand hostile operating environments (rain and saline, humid air). In February 2012, the 2d-ALCA was used for the first time in a test field. The device was mounted in about 53 m above ground level on a lattice tower near the German North Sea coast. Wind speed was measured by the 2d-ALCA at 10 kHz sampling rate and by cup anemometers at 1 Hz. The instantaneous wind speed ranged from 8 m/s to 19 m/s at an average turbulence level of about 7 %. Wind field characteristics were analyzed based on cup anemometer as well as 2d-ALCA. The combination of both devices allowed the study of atmospheric turbulence over several magnitudes in turbulent scales

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

Directory of Open Access Journals (Sweden)

H. A. J. Meijer

2009-09-01

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

Evaluation and Comparison of Chemiluminescence and UV Photometric Methods for Measuring Ozone Concentrations in Ambient Air

Science.gov (United States)

The current Federal Reference Method (FRM) for measuring concentrations of ozone in ambient air is based on the dry, gas-phase, chemiluminescence reaction between ethylene (C2H4) and any ozone (O3) that may be p...

Aerosol Particle Interfacial Thermodynamics and Phase Partitioning Measurements Using Biphasic Microfluidics

Science.gov (United States)

Dutcher, Cari; Metcalf, Andrew

2015-03-01

Secondary organic aerosol particles are nearly ubiquitous in the atmosphere and yet there remain large uncertainties in their formation processes and ambient properties. These particles are complex microenvironments, which can contain multiple interfaces due to internal aqueous-organic phase partitioning and to the external liquid-vapor surface. Interfacial properties affect the ambient aerosol morphology, or internal structure of the particle, which in turn can affect the way a particle interacts with an environment of condensable clusters and organic vapors. To improve our ability to accurately predict ambient aerosol morphology, we must improve our knowledge of aerosol interfaces and their interactions with the ambient environment. Unfortunately, many techniques employed to measure interfacial properties do so in bulk solutions or in the presence of a ternary (e.g. solid) phase. In this talk, a novel method using biphasic microscale flows will be introduced for generating, trapping, and perturbing complex interfaces at atmospherically relevant conditions. These microfluidic experiments utilize high-speed imaging to monitor interfacial phenomena at the microscale and are performed with phase contrast and fluorescence microscopy on a temperature-controlled inverted microscope stage. From these experiments, interfacial thermodynamic properties such as surface or interfacial tension, rheological properties such as interfacial moduli, and kinetic properties such as mass transfer coefficients can be measured or inferred.

A Controlled Environment System For Measuring Plant-Atmosphere Gas Exchange

Science.gov (United States)

James M. Brown

1975-01-01

Describes an inexpensive, efficient system for measuring plant-atmosphere gas exchange. Designed to measure transpiration from potted tree seedlings, it is readily adaptable for measuring other gas exchanges or gas exchange by plant parts. Light level, air and root temperature can be precisely controlled at minimum cost.

An Experimental Measurement on Laminar Burning Velocities and Markstein Length of Iso-Butane-Air Mixtures at Ambient Conditions

Directory of Open Access Journals (Sweden)

Yousif Alaeldeen Altag

2016-01-01

Full Text Available In the present work, experimental investigation on laminar combustion of iso-butane-air mixtures was conducted in constant volume explosion vessel. The experiments were conducted at wide range of equivalence ratios ranging between Ф = 0.6 and 1.4 and atmospheric pressure of 0.1 MPa and ambient temperature of 303K. Using spherically expanding flame method, flame parameters including stretched, unstretched flame propagation speeds, laminar burning velocities and Markstein length were calculated. For laminar burning velocities the method of error bars of 95% confidence level was applied. In addition, values of Markstein lengths were measured in wide range of equivalence ratios to study the influence of stretch rate on flame instability and burning velocity. It was found that the stretched flame speed and laminar burning velocities increased with equivalence ratios and the peak value was obtained at equivalence ratio of Ф = 1.1. The Markstein length decreased with the increases in equivalence ratios, which indicates that the diffusion thermal flame instability increased at high equivalence ratios in richer mixture side. However, the total deviations in the laminar burning velocities have discrepancies of 1.2-2.9% for all investigated mixtures.

Real-time measurements of secondary organic aerosol formation and aging from ambient air in an oxidation flow reactor in the Los Angeles area

Science.gov (United States)

Ortega, Amber M.; Hayes, Patrick L.; Peng, Zhe; Palm, Brett B.; Hu, Weiwei; Day, Douglas A.; Li, Rui; Cubison, Michael J.; Brune, William H.; Graus, Martin; Warneke, Carsten; Gilman, Jessica B.; Kuster, William C.; de Gouw, Joost; Gutiérrez-Montes, Cándido; Jimenez, Jose L.

2016-06-01

Field studies in polluted areas over the last decade have observed large formation of secondary organic aerosol (SOA) that is often poorly captured by models. The study of SOA formation using ambient data is often confounded by the effects of advection, vertical mixing, emissions, and variable degrees of photochemical aging. An oxidation flow reactor (OFR) was deployed to study SOA formation in real-time during the California Research at the Nexus of Air Quality and Climate Change (CalNex) campaign in Pasadena, CA, in 2010. A high-resolution aerosol mass spectrometer (AMS) and a scanning mobility particle sizer (SMPS) alternated sampling ambient and reactor-aged air. The reactor produced OH concentrations up to 4 orders of magnitude higher than in ambient air. OH radical concentration was continuously stepped, achieving equivalent atmospheric aging of 0.8 days-6.4 weeks in 3 min of processing every 2 h. Enhancement of organic aerosol (OA) from aging showed a maximum net SOA production between 0.8-6 days of aging with net OA mass loss beyond 2 weeks. Reactor SOA mass peaked at night, in the absence of ambient photochemistry and correlated with trimethylbenzene concentrations. Reactor SOA formation was inversely correlated with ambient SOA and Ox, which along with the short-lived volatile organic compound correlation, indicates the importance of very reactive (τOH ˜ 0.3 day) SOA precursors (most likely semivolatile and intermediate volatility species, S/IVOCs) in the Greater Los Angeles Area. Evolution of the elemental composition in the reactor was similar to trends observed in the atmosphere (O : C vs. H : C slope ˜ -0.65). Oxidation state of carbon (OSc) in reactor SOA increased steeply with age and remained elevated (OSC ˜ 2) at the highest photochemical ages probed. The ratio of OA in the reactor output to excess CO (ΔCO, ambient CO above regional background) vs. photochemical age is similar to previous studies at low to moderate ages and also extends to

Real-time measurements of secondary organic aerosol formation and aging from ambient air in an oxidation flow reactor in the Los Angeles area

Directory of Open Access Journals (Sweden)

A. M. Ortega

2016-06-01

Full Text Available Field studies in polluted areas over the last decade have observed large formation of secondary organic aerosol (SOA that is often poorly captured by models. The study of SOA formation using ambient data is often confounded by the effects of advection, vertical mixing, emissions, and variable degrees of photochemical aging. An oxidation flow reactor (OFR was deployed to study SOA formation in real-time during the California Research at the Nexus of Air Quality and Climate Change (CalNex campaign in Pasadena, CA, in 2010. A high-resolution aerosol mass spectrometer (AMS and a scanning mobility particle sizer (SMPS alternated sampling ambient and reactor-aged air. The reactor produced OH concentrations up to 4 orders of magnitude higher than in ambient air. OH radical concentration was continuously stepped, achieving equivalent atmospheric aging of 0.8 days–6.4 weeks in 3 min of processing every 2 h. Enhancement of organic aerosol (OA from aging showed a maximum net SOA production between 0.8–6 days of aging with net OA mass loss beyond 2 weeks. Reactor SOA mass peaked at night, in the absence of ambient photochemistry and correlated with trimethylbenzene concentrations. Reactor SOA formation was inversely correlated with ambient SOA and Ox, which along with the short-lived volatile organic compound correlation, indicates the importance of very reactive (τOH  ∼  0.3 day SOA precursors (most likely semivolatile and intermediate volatility species, S/IVOCs in the Greater Los Angeles Area. Evolution of the elemental composition in the reactor was similar to trends observed in the atmosphere (O : C vs. H : C slope  ∼  −0.65. Oxidation state of carbon (OSc in reactor SOA increased steeply with age and remained elevated (OSC  ∼  2 at the highest photochemical ages probed. The ratio of OA in the reactor output to excess CO (ΔCO, ambient CO above regional background vs. photochemical age is similar to

Comparison of halocarbon measurements in an atmospheric dry whole air sample.

Science.gov (United States)

Rhoderick, George C; Hall, Bradley D; Harth, Christina M; Kim, Jin Seog; Lee, Jeongsoon; Montzka, Stephen A; Mühle, Jens; Reimann, Stefan; Vollmer, Martin K; Weiss, Ray F

The growing awareness of climate change/global warming, and continuing concerns regarding stratospheric ozone depletion, will require continued measurements and standards for many compounds, in particular halocarbons that are linked to these issues. In order to track atmospheric mole fractions and assess the impact of policy on emission rates, it is necessary to demonstrate measurement equivalence at the highest levels of accuracy for assigned values of standards. Precise measurements of these species aid in determining small changes in their atmospheric abundance. A common source of standards/scales and/or well-documented agreement of different scales used to calibrate the measurement instrumentation are key to understanding many sets of data reported by researchers. This report describes the results of a comparison study among National Metrology Institutes and atmospheric research laboratories for the chlorofluorocarbons (CFCs) dichlorodifluoromethane (CFC-12), trichlorofluoromethane (CFC-11), and 1,1,2-trichlorotrifluoroethane (CFC-113); the hydrochlorofluorocarbons (HCFCs) chlorodifluoromethane (HCFC-22) and 1-chloro-1,1-difluoroethane (HCFC-142b); and the hydrofluorocarbon (HFC) 1,1,1,2-tetrafluoroethane (HFC-134a), all in a dried whole air sample. The objective of this study is to compare calibration standards/scales and the measurement capabilities of the participants for these halocarbons at trace atmospheric levels. The results of this study show agreement among four independent calibration scales to better than 2.5% in almost all cases, with many of the reported agreements being better than 1.0%.

Comparison of halocarbon measurements in an atmospheric dry whole air sample

Directory of Open Access Journals (Sweden)

George C. Rhoderick

2015-11-01

Full Text Available Abstract The growing awareness of climate change/global warming, and continuing concerns regarding stratospheric ozone depletion, will require continued measurements and standards for many compounds, in particular halocarbons that are linked to these issues. In order to track atmospheric mole fractions and assess the impact of policy on emission rates, it is necessary to demonstrate measurement equivalence at the highest levels of accuracy for assigned values of standards. Precise measurements of these species aid in determining small changes in their atmospheric abundance. A common source of standards/scales and/or well-documented agreement of different scales used to calibrate the measurement instrumentation are key to understanding many sets of data reported by researchers. This report describes the results of a comparison study among National Metrology Institutes and atmospheric research laboratories for the chlorofluorocarbons (CFCs dichlorodifluoromethane (CFC-12, trichlorofluoromethane (CFC-11, and 1,1,2-trichlorotrifluoroethane (CFC-113; the hydrochlorofluorocarbons (HCFCs chlorodifluoromethane (HCFC-22 and 1-chloro-1,1-difluoroethane (HCFC-142b; and the hydrofluorocarbon (HFC 1,1,1,2-tetrafluoroethane (HFC-134a, all in a dried whole air sample. The objective of this study is to compare calibration standards/scales and the measurement capabilities of the participants for these halocarbons at trace atmospheric levels. The results of this study show agreement among four independent calibration scales to better than 2.5% in almost all cases, with many of the reported agreements being better than 1.0%.

Comparison of halocarbon measurements in an atmospheric dry whole air sample

Science.gov (United States)

Hall, Bradley D.; Harth, Christina M.; Kim, Jin Seog; Lee, Jeongsoon; Montzka, Stephen A.; Mühle, Jens; Reimann, Stefan; Vollmer, Martin K.; Weiss, Ray F.

2015-01-01

The growing awareness of climate change/global warming, and continuing concerns regarding stratospheric ozone depletion, will require continued measurements and standards for many compounds, in particular halocarbons that are linked to these issues. In order to track atmospheric mole fractions and assess the impact of policy on emission rates, it is necessary to demonstrate measurement equivalence at the highest levels of accuracy for assigned values of standards. Precise measurements of these species aid in determining small changes in their atmospheric abundance. A common source of standards/scales and/or well-documented agreement of different scales used to calibrate the measurement instrumentation are key to understanding many sets of data reported by researchers. This report describes the results of a comparison study among National Metrology Institutes and atmospheric research laboratories for the chlorofluorocarbons (CFCs) dichlorodifluoromethane (CFC-12), trichlorofluoromethane (CFC-11), and 1,1,2-trichlorotrifluoroethane (CFC-113); the hydrochlorofluorocarbons (HCFCs) chlorodifluoromethane (HCFC-22) and 1-chloro-1,1-difluoroethane (HCFC-142b); and the hydrofluorocarbon (HFC) 1,1,1,2-tetrafluoroethane (HFC-134a), all in a dried whole air sample. The objective of this study is to compare calibration standards/scales and the measurement capabilities of the participants for these halocarbons at trace atmospheric levels. The results of this study show agreement among four independent calibration scales to better than 2.5% in almost all cases, with many of the reported agreements being better than 1.0%. PMID:26753167

Atmospheric Airborne Pressure Measurements Using the Oxygen A Band for the ASCENDS Mission

Science.gov (United States)

Riris, Haris; Rodriguez, Mike; Stephen, Mark; Hasselbrack, William; Allan, Graham; Mao, Jiamping,; Kawa, Stephan R.; Weaver, Clark J.

2011-01-01

We report on airborne atmospheric pressure measurements using new fiber-based laser technology and the oxygen A-band at 765 nm. Remote measurements of atmospheric temperature and pressure are required for a number of NASA Earth science missions and specifically for the Active Sensing of CO2 Emissions Over Nights, Days, and Seasons (ASCENDS) mission. Accurate measurements of tropospheric CO2 on a global scale are very important in order to better understand its sources and sinks and to improve predictions on any future climate change. The ultimate goal of a CO2 remote sensing mission, such as ASCENDS, is to derive the CO2 concentration in the atmosphere in terms of mole fraction in unit of parts-per-million (ppmv) with regard to dry air. Therefore, both CO2 and the dry air number of molecules in the atmosphere are needed in deriving this quantity. O2 is a stable molecule and uniformly mixed in the atmosphere. Measuring the O2 absorption in the atmosphere can thus be used to infer the dry air number of molecules and then used to calculate CO2 concentration. With the knowledge of atmospheric water vapor, we can then estimate the total surface pressure needed for CO2 retrievals. Our work, funded by the ESTO IIP program, uses fiber optic technology and non-linear optics to generate 765 nm laser radiation coincident with the Oxygen A-band. Our pulsed, time gated technique uses several on- and off-line wavelengths tuned to the O2 absorption line. The choice of wavelengths allows us to measure the pressure by using two adjacent O2 absorptions in the Oxygen A-band. Our retrieval algorithm fits the O2 lineshapes and derives the pressure. Our measurements compare favorably with a local weather monitor mounted outside our laboratory and a local weather station.

Science Plan for the Atmospheric Radiation Measurement Program (ARM)

International Nuclear Information System (INIS)

1996-02-01

The purpose of this Atmospheric Radiation Measurement (ARM) Science Plan is to articulate the scientific issues driving the ARM Program, and to relate them to DOE's programmatic objectives for ARM, based on the experience and scientific progress gained over the past five years. ARM programmatic objectives are to: (1) Relate observed radiative fluxes and radiances in the atmosphere, spectrally resolved and as a function of position and time, to the temperature and composition of the atmosphere, specifically including water vapor and clouds, and to surface properties, and sample sufficient variety of situations so as to span a wide range of climatologically relevant possibilities; (2) develop and test parameterizations that can be used to accurately predict the radiative properties and to model the radiative interactions involving water vapor and clouds within the atmosphere, with the objective of incorporating these parameterizations into general circulation models. The primary observational methods remote sending and other observations at the surface, particularly remote sensing of clouds, water vapor and aerosols

HO2 measurements at atmospheric concentrations using a chemical ionization mass spectrometry

Science.gov (United States)

Albrecht, S.; Novelli, A.; Hofzumahaus, A.; Kang, S.; Baker, Y.; Mentel, T. F.; Fuchs, H.

2017-12-01

Correct and precise measurements of atmospheric radical species are necessary for a better understanding of the oxidative capacity of the atmosphere. Due to the reactivity of radicals, and their consequent low concentrations, direct measurements of these species are particularly challenging and have been proven in the past to be affected by interfering species. Here we present a chemical ionization source coupled to an APi-HR-TOF-MS (Aerodyne Research Inc.), which has a limit of detection for HO2 radicals well below its atmospheric concentrations ( 1 x 108 molecules cm-3). The instrument was calibrated with a well-established and characterized HO2 calibration source in use for the laser induced fluorescence instrument in the Forschungszentrum Jülich. Within the source, a well characterized amount of HO2 radicals is produced after photolysis of water by a mercury lamp. In addition, several experiments were performed in the atmosphere simulation chamber SAPHIR at the Forschungszentrum Jülich to test for potential interferences. Measurements of HO2 radicals were concurrently detected by a laser induced fluorescence instrument allowing for the comparison of measurements within the two different and independent techniques for various atmospheric conditions regarding concentrations of O3, NOx and VOCs. Results from the intercomparison together with the calibration procedure of the instrument and laboratory characterization will be presented.

Applications of high power microwaves to atmospheric modification and measurement

International Nuclear Information System (INIS)

Benford, J.

1993-01-01

The current state of proposals to use high power microwaves in the atmosphere is reviewed. HPM has been proposed to aid in the conservation of stratospheric ozone by partial breakdown, facilitating chemistry to eliminate chlorine. Another proposal is over-the-horizon radar using a partial breakdown area in the ionosphere. A key to any such effort is rapid diagnosis of the state of the atmosphere before, during and after intervention. Technology requirements of these modification and measurement proposals are reviewed. The elements of an atmospheric modification program are identified and political, economic and ideological factors are discussed

Evaluation of Routine Atmospheric Sounding Measurements using Unmanned Systems (ERASMUS)

Energy Technology Data Exchange (ETDEWEB)

Bland, Geoffrey [NASA Goddard Space Flight Center (GSFC), Greenbelt, MD (United States)

2016-06-30

The use of small unmanned aircraft systems (sUAS) with miniature sensor systems for atmospheric research is an important capability to develop. The Evaluation of Routine Atmospheric Sounding Measurements using Unmanned Systems (ERASMUS) project, lead by Dr. Gijs de Boer of the Cooperative Institute for Research in Environmental Sciences (CIRES- a partnership of NOAA and CU-Boulder), is a significant milestone in realizing this new potential. This project has clearly demonstrated that the concept of sUAS utilization is valid, and miniature instrumentation can be used to further our understanding of the atmospheric boundary layer in the arctic.

SOA formation from gasoline vehicles: from the tailpipe to the atmosphere

Science.gov (United States)

Robinson, A. L.; Zhao, Y.; Lambe, A. T.; Saleh, R.; Saliba, G.; Tkacik, D. S.

2017-12-01

Secondary organic aerosol (SOA) formation from gasoline vehicles has been indicated as an important source of atmospheric SOA, but its contribution to atmospheric SOA is loosely constrained due to the lack of measurements to link SOA formation from the tailpipe to atmospheric SOA. In this study, we determine the contribution of SOA formation based on measurements made with a Potential Aerosol Mass (PAM) oxidation flow reactor by oxidizing vehicular exhaust and ambient air. We first investigate SOA formation from dilute gasoline-vehicle exhaust during chassis dynamometer testing. The test fleet consists of both vehicles equipped with gasoline direct injection engines (GDI vehicles) and those equipped with port fuel injection engines (PFI vehicles). These vehicles span a wide range of emissions standards from Tier0 to Super Ultra-Low Emission Vehicles (SULEV). Then, we combine our measurements of SOA formation from gasoline vehicles during dynamometer testing with measurements of SOA formation using a PAM reactor conducted in a highway tunnel and in the unban atmosphere. Comparisons of SOA formation between these datasets enable us to quantitatively connect SOA formation from individual vehicles, to a large on-road fleet, and to the atmosphere. To facilitate the comparisons, we account for the effects of both the photochemical age and dilution on SOA formation. Our results show that SOA formation from gasoline vehicles can contribute over 50% of fossil fuel-related atmospheric SOA in the Los Angeles area. Furthermore, our results demonstrate that the tightening of emissions standards effectively reduces SOA formation from gasoline vehicles, including both PFI and GDI vehicles, if the atmospheric chemistry regime remains the same.

Seasonal variation of heavy metals in ambient air and precipitation at a single site in Washington, DC

International Nuclear Information System (INIS)

Melaku, Samuel; Morris, Vernon; Raghavan, Dharmaraj; Hosten, Charles

2008-01-01

Atmospheric samples of precipitation and ambient air were collected at a single site in Washington, DC, for 7 months (for ambient air samples) and 1 year (for wet deposition samples) and analyzed for arsenic, cadmium, chromium and lead. The ranges of heavy metal concentrations for 6-day wet deposition samples collected over the 1-year period were 0.20-1.3 μg/l, 0.060-5.1 μg/l, 0.062-4.6 μg/l and 0.11-3.2 μg/l for arsenic, cadmium, chromium and lead, respectively, with a precision better than 5% for more than 95% of the measurements. The ranges of heavy metal concentrations for the 6-day ambient air samples were 0.800-15.7 ng/m 3 , 1.50-30.0 ng/m 3 , 16.8-112 ng/m 3 , and 2.90-137 ng/m 3 for arsenic, cadmium, chromium and lead, respectively, with a precision better than 10%. The spread in the heavy metal concentration over the observation period suggests a high seasonal variability for heavy metal content in both ambient air and wet deposition samples. - High seasonal variability of heavy metals were observed in both ambient air and wet deposition samples

Ambient and Wake Turbulence Measurements at Marine Energy Sites from a Five Beam AD2CP

Science.gov (United States)

Guerra, M. A.; Thomson, J. M.

2016-02-01

Ambient turbulence at hydrokinetic energy sites is a key input for turbine design and for their performance determination. Added turbulence from rotating blades to the flow affects the environment surrounding the turbine and has an impact in turbine array distribution. We present two approaches of turbulence measurements: stationary and drifting. Stationary measurements allow for time and frequency analysis of turbulent velocities, while drifting measurements give a spatial characterization of turbulence. For both approaches we used the new five beam Nortek Signature AD2CP. This instrument captures turbulent flow along the water column at high sampling rates (8 Hz) with low Doppler noise level; the use of five beams also makes it possible to fully calculate the Reynolds Stresses. Both sets of measurements require Doppler noise removal for consistent results. Stationary measurements of ambient turbulence were carried out in Admiralty Inlet, WA, in May 2015. The Signature was deployed up looking on a sea spider tripod in a 50 m depth tidal channel during two tidal cycles. This data set allowed us to characterize the turbulence in terms of spectra and Reynolds Stresses in order to evaluate the turbulent kinetic energy balance along the water column and to compare results to other tidal energy sites with similar characteristics where turbulence measurements were taken as well. Drifting measurements of ambient and wake turbulence were conducted in the vicinity of the ORPC RivGen® turbine deployed on the Kvichak River in Alaska in July 2015. The Signature was mounted down looking onboard an anchor buoy equipped with two GPS data receivers for georefference. The cross-sectional river span was covered by releasing the drifter at different positions across the river. More than 300 drifts were performed to spatially characterize turbulence before and after turbine's deployment and grid connection. Results indicate an increased turbulent wake extending up to 75 m downstream

Source identification of ambient PM2.5 during summer inhalation exposure studies in Detroit, MI

Energy Technology Data Exchange (ETDEWEB)

Morishita, M.; Keeler, G.J.; Wagner, J.G.; Harkema, J.R. [University of Michigan, Ann Arbor, MI (United States). Air Quality Laboratory

2006-07-15

Particulate air pollution is associated with cardiopulmonary morbidity and mortality in heavily populated urban centers of the United States. Because ambient fine particulate matter (aerodynamic diameter {<=} 2.5 {mu}m; PM2.5) is a complex mixture resulting from multiple sources and variable atmospheric conditions, it is difficult to identify specific components of PM2.5 that are responsible for adverse health effects. During four consecutive summers from 2000 to 2003 we characterized the ambient gaseous and PM2.5 air quality in an urban southwest Detroit community where childhood asthma hospitalization rates are more than twice the statewide average. Both integrated and continuous PM measurements together with gaseous air pollution measurements were performed using a mobile air research facility, AirCARE1, in which concurrent toxicological studies were being conducted. Chemical and physical characterizations of PM2.5 as well as receptor modeling using positive matrix factorization (PMF) were completed. Results from PMF indicated that six major sources contributed to the observed ambient PM2.5 mass during the summer months. Primary sources included (1) coal combustion/secondary sulfate aerosol, (2) motor vehicle/urban road dust, (3) municipal waste incinerators, (4) oil combustion/refineries, (5) sewage sludge incinerators, and (6) iron/steel manufacturing. Although the contribution of the coal/secondary sulfate aerosol source was greater than other factors, increased levels of urban PM2.5 from local combustion sources were also observed. In addition to characterization of ambient PM2.5 and their sources in southwest Detroit, this paper discusses possible associations of ambient PM2.5 from local combustion sources, specifically incinerator and refinery emissions and the observed adverse health effects during the inhalation exposure campaigns.

Microplasma-based flowing atmospheric-pressure afterglow (FAPA) source for ambient desorption-ionization mass spectrometry

Energy Technology Data Exchange (ETDEWEB)

Zeiri, Offer M.; Storey, Andrew P.; Ray, Steven J., E-mail: sjray2@buffalo.edu; Hieftje, Gary M.

2017-02-01

A new direct-current microplasma-based flowing atmospheric pressure afterglow (FAPA) source was developed for use in ambient desorption-ionization mass spectrometry. The annular-shaped microplasma is formed in helium between two concentric stainless-steel capillaries that are separated by an alumina tube. Current-voltage characterization of the source shows that this version of the FAPA operates in the normal glow-discharge regime. A glass surface placed in the path of the helium afterglow reaches temperatures of up to approximately 400 °C; the temperature varies with distance from the source and helium flow rate through the source. Solid, liquid, and vapor samples were examined by means of a time-of-flight mass spectrometer. Results suggest that ionization occurs mainly through protonation, with only a small amount of fragmentation and adduct formation. The mass range of the source was shown to extend up to at least m/z 2722 for singly charged species. Limits of detection for several small organic molecules were in the sub-picomole range. Examination of competitive ionization revealed that signal suppression occurs only at high (mM) concentrations of competing substances. - Highlights: • The first microplasma version of the FAPA source. • Current-voltage behavior reflects the behavior of a normal glow discharge. • Detection limits below 1 pmol for the classes of organic compounds studied over a wide mass range. • Mass spectra show limited fragmentation.

A condensed water method for measuring the atmospheric radon

CERN Document Server

Wu Xin; Pan Xiao Qing; Yu Yi Ling

1998-01-01

The author summarizes the present situation of atmospheric Radon measurement, and introduces the working principle, working method and advantage and disadvantage of condensed water method in detail. The structure and function of the instrument used for this method, and the measuring result are discussed. The direction of further work is pointed out from now on

Joint measurements of PM2. 5 and light-absorptive PM in woodsmoke-dominated ambient and plume environments

Science.gov (United States)

Zhang, K. Max; Allen, George; Yang, Bo; Chen, Geng; Gu, Jiajun; Schwab, James; Felton, Dirk; Rattigan, Oliver

2017-09-01

DC, also referred to as Delta-C, measures enhanced light absorption of particulate matter (PM) samples at the near-ultraviolet (UV) range relative to the near-infrared range, which has been proposed previously as a woodsmoke marker due to the presence of enhanced UV light-absorbing materials from wood combustion. In this paper, we further evaluated the applications and limitations of using DC as both a qualitative and semi-quantitative woodsmoke marker via joint continuous measurements of PM2. 5 (by nephelometer pDR-1500) and light-absorptive PM (by 2-wavelength and 7-wavelength Aethalometertext">®) in three northeastern US cities/towns including Rutland, VT; Saranac Lake, NY and Ithaca, NY. Residential wood combustion has shown to be the predominant source of wintertime primary PM2. 5 emissions in both Rutland and Saranac Lake, where we conducted ambient measurements. In Ithaca, we performed woodsmoke plume measurements. We compared the pDR-1500 against a FEM PM2. 5 sampler (BAM 1020), and identified a close agreement between the two instruments in a woodsmoke-dominated ambient environment. The analysis of seasonal and diurnal trends of DC, black carbon (BC, 880 nm) and PM2. 5 concentrations supports the use of DC as an adequate qualitative marker. The strong linear relationships between PM2. 5 and DC in both woodsmoke-dominated ambient and plume environments suggest that DC can reasonably serve as a semi-quantitative woodsmoke marker. We propose a DC-based indicator for woodsmoke emission, which has shown to exhibit a relatively strong linear relationship with heating demand. While we observed reproducible PM2. 5-DC relationships in similar woodsmoke-dominated ambient environments, those relationships differ significantly with different environments, and among individual woodsmoke sources. Our analysis also indicates the potential for PM2. 5-DC relationships to be utilized to distinguish different combustion and operating conditions of woodsmoke sources, and

Passive radiative cooling below ambient air temperature under direct sunlight.

Science.gov (United States)

Raman, Aaswath P; Anoma, Marc Abou; Zhu, Linxiao; Rephaeli, Eden; Fan, Shanhui

2014-11-27

Cooling is a significant end-use of energy globally and a major driver of peak electricity demand. Air conditioning, for example, accounts for nearly fifteen per cent of the primary energy used by buildings in the United States. A passive cooling strategy that cools without any electricity input could therefore have a significant impact on global energy consumption. To achieve cooling one needs to be able to reach and maintain a temperature below that of the ambient air. At night, passive cooling below ambient air temperature has been demonstrated using a technique known as radiative cooling, in which a device exposed to the sky is used to radiate heat to outer space through a transparency window in the atmosphere between 8 and 13 micrometres. Peak cooling demand, however, occurs during the daytime. Daytime radiative cooling to a temperature below ambient of a surface under direct sunlight has not been achieved because sky access during the day results in heating of the radiative cooler by the Sun. Here, we experimentally demonstrate radiative cooling to nearly 5 degrees Celsius below the ambient air temperature under direct sunlight. Using a thermal photonic approach, we introduce an integrated photonic solar reflector and thermal emitter consisting of seven layers of HfO2 and SiO2 that reflects 97 per cent of incident sunlight while emitting strongly and selectively in the atmospheric transparency window. When exposed to direct sunlight exceeding 850 watts per square metre on a rooftop, the photonic radiative cooler cools to 4.9 degrees Celsius below ambient air temperature, and has a cooling power of 40.1 watts per square metre at ambient air temperature. These results demonstrate that a tailored, photonic approach can fundamentally enable new technological possibilities for energy efficiency. Further, the cold darkness of the Universe can be used as a renewable thermodynamic resource, even during the hottest hours of the day.

Chapter 4 Gaseous Elemental Mercury in the Ambient Atmosphere

DEFF Research Database (Denmark)

Ariya, Parisa A.; Skov, Henrik; Grage, Mette M L

2008-01-01

Understanding the kinetics and mechanisms associated with the atmospheric chemistry of mercury is of great importance to protecting the environment. This review will focus on theoretical calculations to advance understanding of gas phase oxidation of gaseous elemental mercury (GEM) by halogen spe...

Secondary organic aerosol formation from ambient air in an oxidation flow reactor in central Amazonia

Directory of Open Access Journals (Sweden)

B. B. Palm

2018-01-01

Full Text Available Secondary organic aerosol (SOA formation from ambient air was studied using an oxidation flow reactor (OFR coupled to an aerosol mass spectrometer (AMS during both the wet and dry seasons at the Observations and Modeling of the Green Ocean Amazon (GoAmazon2014/5 field campaign. Measurements were made at two sites downwind of the city of Manaus, Brazil. Ambient air was oxidized in the OFR using variable concentrations of either OH or O3, over ranges from hours to days (O3 or weeks (OH of equivalent atmospheric aging. The amount of SOA formed in the OFR ranged from 0 to as much as 10 µg m−3, depending on the amount of SOA precursor gases in ambient air. Typically, more SOA was formed during nighttime than daytime, and more from OH than from O3 oxidation. SOA yields of individual organic precursors under OFR conditions were measured by standard addition into ambient air and were confirmed to be consistent with published environmental chamber-derived SOA yields. Positive matrix factorization of organic aerosol (OA after OH oxidation showed formation of typical oxidized OA factors and a loss of primary OA factors as OH aging increased. After OH oxidation in the OFR, the hygroscopicity of the OA increased with increasing elemental O : C up to O : C ∼ 1.0, and then decreased as O : C increased further. Possible reasons for this decrease are discussed. The measured SOA formation was compared to the amount predicted from the concentrations of measured ambient SOA precursors and their SOA yields. While measured ambient precursors were sufficient to explain the amount of SOA formed from O3, they could only explain 10–50 % of the SOA formed from OH. This is consistent with previous OFR studies, which showed that typically unmeasured semivolatile and intermediate volatility gases (that tend to lack C = C bonds are present in ambient air and can explain such additional SOA formation. To investigate the sources of the

Venus thermosphere and exosphere - First satellite drag measurements of an extraterrestrial atmosphere

Science.gov (United States)

Keating, G. M.; Tolson, R. H.; Hinson, E. W.

1979-01-01

Atmospheric drag measurements obtained from the study of the orbital decay of Pioneer Venus I indicate that atomic oxygen predominates in the Venus atmosphere above 160 kilometers. Drag measurements give evidence that conditions characteristic of a planetary thermosphere disappear near sundown, with inferred exospheric temperatures sharply dropping from approximately 300 K to less than 150 K. Observed densities are generally lower than given by theoretical models.

Measurements and theoretical calculations of diffused radiation and atmosphere lucidity

International Nuclear Information System (INIS)

Pelece, I.; Iljins, U.; Ziemelis, I.

2009-01-01

Align with other environment friendly renewable energy sources solar energy is widely used in the world. Also in Latvia solar collectors are used. However, in Latvia because of its geographical and climatic conditions there are some specific features in comparison with traditional solar energy using countries. These features lead to the necessity to pay more attention to diffused irradiance. Another factor affecting the received irradiance of any surface is lucidity of atmosphere. This factor has not been studied in Latvia yet. This article deals with evaluation of diffused irradiance, and also of lucidity of atmosphere. The diffused irradiance can be measured directly or as a difference between the global irradiance and the beam one. The lucidity of atmosphere can be calculated from the measurements of both global and beam irradiance, if the height of the sun is known. Therefore, measurements of both global and beam irradiance have been carried out, and the diffused irradiance calculated as a difference between the global irradiance and the beam one. For measuring of the global irradiance the dome solarimeter has been used. For measuring of the direct irradiance tracking to sun pirheliometer has been used. The measurements were performed in Riga from October 2008 till March 2009. The measurements were executed automatically after every 5 minutes. The obtained results have been analyzed taking into account also the data on nebulosity from the State agency Latvian Environment, Geology and Meteorology Agency. Also efforts to calculate theoretically the diffused irradiance from the height of the sun and the data of the nebulosity have been done. These calculated values have been compared with the measured ones. Good accordance is obtained. (author)

Collisionless coupling of a high- β expansion to an ambient, magnetized plasma. II. Experimental fields and measured momentum coupling

Science.gov (United States)

Bonde, Jeffrey; Vincena, Stephen; Gekelman, Walter

2018-04-01

The momentum coupled to a magnetized, ambient argon plasma from a high- β, laser-produced carbon plasma is examined in a collisionless, weakly coupled limit. The total electric field was measured by separately examining the induced component associated with the rapidly changing magnetic field of the high- β (kinetic β˜106), expanding plasma and the electrostatic component due to polarization of the expansion. Their temporal and spatial structures are discussed and their effect on the ambient argon plasma (thermal β˜10-2) is confirmed with a laser-induced fluorescence diagnostic, which directly probed the argon ion velocity distribution function. For the given experimental conditions, the electrostatic field is shown to dominate the interaction between the high- β expansion and the ambient plasma. Specifically, the expanding plasma couples energy and momentum into the ambient plasma by pulling ions inward against the flow direction.

Seasonal Variation of Atmospheric Composition of Water-Soluble ...

African Journals Online (AJOL)

`123456789jkl''''#

Background Site in Tanzania, East Africa. 1Mkoma S.L. ... fine, coarse and PM10 mass were, 17±4, 52±27 and 69±29 µg/m3 during the 2005 dry season campaign and. 13±5, 34±23 ... particles in ambient air, atmospheric particulate ... especially the fine particle fraction with ..... Atmospheric Chemistry and Physics: From Air.

The sound of high winds. The effect of atmospheric stability on wind turbine sound and microphone noise

International Nuclear Information System (INIS)

Van den Berg, G.P.

2006-01-01

In this thesis issues are raised concerning wind turbine noise and its relationship to altitude dependent wind velocity. The following issues are investigated: what is the influence of atmospheric stability on the speed and sound power of a wind turbine?; what is the influence of atmospheric stability on the character of wind turbine sound?; how widespread is the impact of atmospheric stability on wind turbine performance: is it relevant for new wind turbine projects; how can noise prediction take this stability into account?; what can be done to deal with the resultant higher impact of wind turbine sound? Apart from these directly wind turbine related issues, a final aim was to address a measurement problem: how does wind on a microphone affect the measurement of the ambient sound level?

Effect of Atmospheric Conditions on LIBS Spectra

OpenAIRE

Effenberger, Andrew J.; Scott, Jill R.

2010-01-01

Laser-induced breakdown spectroscopy (LIBS) is typically performed at ambient Earth atmospheric conditions. However, interest in LIBS in other atmospheric conditions has increased in recent years, especially for use in space exploration (e.g., Mars and Lunar) or to improve resolution for isotopic signatures. This review focuses on what has been reported about the performance of LIBS in reduced pressure environments as well as in various gases other than air.

Scintillation detectors, applications in ambient dose rate measurement of ionizing radiation

International Nuclear Information System (INIS)

Harja, C.

1997-01-01

For the task of developing an ambient dose rate measuring probe, the company MAB decided for a design combining an organic plastic scintillator and a secondary electron multiplier. MAB tested a range of available plastic scintillators suitable for this task, and one proved to be particularly good for the intended purpose. This scintillator is a product of the British company NE Technology Ltd. and was specially developed for dosimetry applications, offering the following advantages: The response within the range from 33 keV to 1.3 MeV (Co-60) is much more constant than with combined-design types; there is no afterglow under conditions of excessive load. (orig./CB) [de

Gone with the Wind: Three Years of MAVEN Measurements of Atmospheric Loss at Mars

Science.gov (United States)

Brain, David; MAVEN Team

2017-10-01

The Mars Atmosphere and Volatile EvolutioN (MAVEN) mission is making measurements of the Martian upper atmosphere and near space environment, and their interactions with energy inputs from the Sun. A major goal of the mission is to evaluate the loss of atmospheric gases to space in the present epoch, and over Martian history. MAVEN is equipped with instruments that measure both the neutral and charged upper atmospheric system (thermosphere, ionosphere, exosphere, and magnetosphere), inputs from the Sun (extreme ultraviolet flux, solar wind and solar energetic particles, and interplanetary magnetic field), and escaping atmospheric particles. The MAVEN instruments, coupled with models, allow us to more completely understand the physical processes that control atmospheric loss and the particle reservoirs for loss.Here, we provide an overview of the significant results from MAVEN over approximately 1.5 Mars years (nearly three Earth years) of observation, from November 2014 to present. We argue that the MAVEN measurements tell us that the loss of atmospheric gases to space was significant over Martian history, and present the seasonal behavior of the upper atmosphere and magnetosphere. We also discuss the influence of extreme events such as solar storms, and a variety of new discoveries and observations of the Martian system made by MAVEN.

Olfactory marketing: The role of ambient scents in a shopping experience

OpenAIRE

Douce, Lieve

2015-01-01

Atmospheric elements such as lights, music, and scents make up the physical environment of a store and can have an impact on consumers’ shopping behavior. This doctoral dissertation aims to provide a better understanding of the effects of ambient scent in the store environment on consumer reactions. Specifically, the moderating role of individual differences (chapter 2 and 3), product congruency (chapter 4 and 5) and congruency with other atmospheric elements (chapter 6 and 7) on scent effect...

Measurements of atmospheric and gamma rays-balloon experiments at subantartic region

International Nuclear Information System (INIS)

Jayanthi, U.B.; Correa, R.V.; Blanco, F.G.

1986-01-01

The results of two stratospheric balloon experiments conducted to measure the atmospheric X and gamma rays are presented. These experiments, conducted at Comandante Ferraz base in subantarctic region, have provided the spectrum of ground radioactivity in gamma rays (0.2 to 2.9 MeV) and atmospheric X-ray spectra at different altitudes. We specifically chose to discuss the observed ceiling spectrum of X-rays in the 28 to 180KeV region observed at 7.0 g. cm -2 . We have utilized the data of other experiments with different telescope geometries, to evaluate the builup effects due to cosmic ray secondaries in atmosphere. This behaviour, previoulsy studied for atmospheric gamma rays, permitted to compare the up/down flux rations to explain the observed atmospheric X-ray spectrum. (Author) [pt

TRANC – a novel fast-response converter to measure total reactive atmospheric nitrogen

Directory of Open Access Journals (Sweden)

V. Wolff

2012-05-01

Full Text Available The input and loss of plant available nitrogen (reactive nitrogen: Nr from/to the atmosphere can be an important factor for the productivity of ecosystems and thus for its carbon and greenhouse gas exchange. We present a novel converter for reactive nitrogen (TRANC: Total Reactive Atmospheric Nitrogen Converter, which offers the opportunity to quantify the sum of all airborne reactive nitrogen compounds (∑Nr in high time resolution. The basic concept of the TRANC is the full conversion of all Nr to nitrogen monoxide (NO within two reaction steps. Initially, reduced Nr compounds are being oxidised, and oxidised Nr compounds are thermally converted to lower oxidation states. Particulate Nr is being sublimated and oxidised or reduced afterwards. In a second step, remaining higher nitrogen oxides or those generated in the first step are catalytically converted to NO with carbon monoxide used as reduction gas. The converter is combined with a fast response chemiluminescence detector (CLD for NO analysis and its performance was tested for the most relevant gaseous and particulate Nr species under both laboratory and field conditions. Recovery rates during laboratory tests for NH3 and NO2 were found to be 95 and 99%, respectively, and 97% when the two gases were combined. In-field longterm stability over an 11-month period was approved by a value of 91% for NO2. Effective conversion was also found for ammonium and nitrate containing particles. The recovery rate of total ambient Nr was tested against the sum of individual measurements of NH3, HNO3, HONO, NH4+, NO3−, and NOx using a combination of different well-established devices. The results show that the TRANC-CLD system precisely captures fluctuations in ∑Nr concentrations and also matches the sum of all individual Nr compounds measured by the different single techniques. The TRANC features a specific design with very short distance between the sample air inlet and the place where the thermal

Secondary organic aerosol formation from in situ OH, O3, and NO3 oxidation of ambient forest air in an oxidation flow reactor

Science.gov (United States)

Palm, Brett B.; Campuzano-Jost, Pedro; Day, Douglas A.; Ortega, Amber M.; Fry, Juliane L.; Brown, Steven S.; Zarzana, Kyle J.; Dube, William; Wagner, Nicholas L.; Draper, Danielle C.; Kaser, Lisa; Jud, Werner; Karl, Thomas; Hansel, Armin; Gutiérrez-Montes, Cándido; Jimenez, Jose L.

2017-04-01

Ambient pine forest air was oxidized by OH, O3, or NO3 radicals using an oxidation flow reactor (OFR) during the BEACHON-RoMBAS (Bio-hydro-atmosphere interactions of Energy, Aerosols, Carbon, H2O, Organics and Nitrogen - Rocky Mountain Biogenic Aerosol Study) campaign to study biogenic secondary organic aerosol (SOA) formation and organic aerosol (OA) aging. A wide range of equivalent atmospheric photochemical ages was sampled, from hours up to days (for O3 and NO3) or weeks (for OH). Ambient air processed by the OFR was typically sampled every 20-30 min, in order to determine how the availability of SOA precursor gases in ambient air changed with diurnal and synoptic conditions, for each of the three oxidants. More SOA was formed during nighttime than daytime for all three oxidants, indicating that SOA precursor concentrations were higher at night. At all times of day, OH oxidation led to approximately 4 times more SOA formation than either O3 or NO3 oxidation. This is likely because O3 and NO3 will only react with gases containing C = C bonds (e.g., terpenes) to form SOA but will not react appreciably with many of their oxidation products or any species in the gas phase that lacks a C = C bond (e.g., pinonic acid, alkanes). In contrast, OH can continue to react with compounds that lack C = C bonds to produce SOA. Closure was achieved between the amount of SOA formed from O3 and NO3 oxidation in the OFR and the SOA predicted to form from measured concentrations of ambient monoterpenes and sesquiterpenes using published chamber yields. This is in contrast to previous work at this site (Palm et al., 2016), which has shown that a source of SOA from semi- and intermediate-volatility organic compounds (S/IVOCs) 3.4 times larger than the source from measured VOCs is needed to explain the measured SOA formation from OH oxidation. This work suggests that those S/IVOCs typically do not contain C = C bonds. O3 and NO3 oxidation produced SOA with elemental O : C and H : C

Desorption atmospheric pressure photoionization high-resolution mass spectrometry: a complementary approach for the chemical analysis of atmospheric aerosols.

Science.gov (United States)

Parshintsev, Jevgeni; Vaikkinen, Anu; Lipponen, Katriina; Vrkoslav, Vladimir; Cvačka, Josef; Kostiainen, Risto; Kotiaho, Tapio; Hartonen, Kari; Riekkola, Marja-Liisa; Kauppila, Tiina J

2015-07-15

On-line chemical characterization methods of atmospheric aerosols are essential to increase our understanding of physicochemical processes in the atmosphere, and to study biosphere-atmosphere interactions. Several techniques, including aerosol mass spectrometry, are nowadays available, but they all suffer from some disadvantages. In this research, desorption atmospheric pressure photoionization high-resolution (Orbitrap) mass spectrometry (DAPPI-HRMS) is introduced as a complementary technique for the fast analysis of aerosol chemical composition without the need for sample preparation. Atmospheric aerosols from city air were collected on a filter, desorbed in a DAPPI source with a hot stream of toluene and nitrogen, and ionized using a vacuum ultraviolet lamp at atmospheric pressure. To study the applicability of the technique for ambient aerosol analysis, several samples were collected onto filters and analyzed, with the focus being on selected organic acids. To compare the DAPPI-HRMS data with results obtained by an established method, each filter sample was divided into two equal parts, and the second half of the filter was extracted and analyzed by liquid chromatography/mass spectrometry (LC/MS). The DAPPI results agreed with the measured aerosol particle number. In addition to the targeted acids, the LC/MS and DAPPI-HRMS methods were found to detect different compounds, thus providing complementary information about the aerosol samples. DAPPI-HRMS showed several important oxidation products of terpenes, and numerous compounds were tentatively identified. Thanks to the soft ionization, high mass resolution, fast analysis, simplicity and on-line applicability, the proposed methodology has high potential in the field of atmospheric research. Copyright © 2015 John Wiley & Sons, Ltd.

A passive sampler for atmospheric ozone

International Nuclear Information System (INIS)

Grosjean, D.; Hisham, M.W.M.

1992-01-01

A simple, cost-effective passive sampler has been developed for the determination of atmospheric ozone. This passive sampler is based on a colorant which fades upon reaction with ozone, whose concentration can be determined by reflectance measurement of the color change. Direct, on-site measurements are possible, and no chemical analyses are needed. Sampler design and validation studies have been carried out and included quantitative determination of color change vs exposure time (1-8 days), color change vs. ozone concentration (30-350 ppb), and response to changes in sampler configuration that modify the passive sampling rate. With indigo carmine as the colorant, the detection limits are 30 ppb. day and 120 ppb. day using a plastic grid and Teflon filter, respectively, as diffusion barriers. Interferences from nitrogen dioxide, formaldehyde and peroxyacetyl nitrate are 15, 4 and 16%, respectively, thus resulting in a negligible bias when measuring ozone in ambient air

THE EFFECTS OF AMBIENT SCENT ON CONSUMER BEHAVIOR: A REVIEW OF THE LITERATURE

Directory of Open Access Journals (Sweden)

OLAHUT Meda Roxana

2013-07-01

Full Text Available The main purpose of this paper is to present an extended literature review of relevant empirical studies which examine the effect of ambient scent on consumers' perception, consumers' emotions and consumers' behavioral responses in the context of retailing. Compared with other atmospheric stimuli (such as background music, ambient scent has received little attention from researchers. This paper is also concentrated on identifying de principal dimensions of ambient scent (presence versus absence; congruity versus incongruity and pleasantness versus unpleasantness and examined how these dimensions of ambient scent have an impact on evaluation of a product, of a store or of a shopping mall and their impact on shopping behavior within a store. The paper also presented the Gulas and Bloch (1995 model, a complex conceptual framework on the influence of ambient scent on consumer responses, in their model the authors introduced the influence of mediating factors on behavioral responses to scent. Their model is a first step on the understanding the role of ambient scent in influencing consumer behavior. Davis, Kooijman and Ward (2003 extending and elaborating the Gulas and Bloch (1995 model by introducing concepts from cognate disciplines and examines mediating factors that help shape the emotional and behavioural responses that are stimulated to encompass current research on human olfaction and brings another specific points for future research. Based on the results of the relevant studies the authors of the present paper concludes by identifying gaps in the literature and suggest future research to explore how the use of scent help to create an overall store atmosphere which influence shopping behavior in the context of retailing.

Telemetric measurement system of beehive environment conditions

Science.gov (United States)

Walendziuk, Wojciech; Sawicki, Aleksander

2014-11-01

This work presents a measurement system of beehive environmental conditions. The purpose of the device is to perform measurements of parameters such as ambient temperature, atmospheric pressure, internal temperature, humidity and sound level. The measured values were transferred to the MySQL database, which is located on an external server, with the use of GPRS protocol. A website presents the measurement data in the form of tables and graphs. The study also shows exemplary results of environmental conditions measurements recorded in the beehive by hour cycle.

Atmospheric diffusion wind tunnel with automatic measurement

Energy Technology Data Exchange (ETDEWEB)

Maki, S; Sakai, J; Murata, E

1974-01-01

A wind tunnel which permits estimates of atmospheric diffusion is described. Smoke from power plant smoke stacks, for example, can be simulated and traced to determine the manner of diffusion in the air as well as the grade of dilution. The wind tunnel is also capable of temperature controlled diffusion tests in which temperature distribution inside the wind tunnel is controlled. A minimum wind velocity of 10 cm can be obtained with accuracy within plus or minus 0.05 percent using a controlled direct current motor; diffusion tests are often made at low wind velocity. Fully automatic measurements can be obtained by using a minicomputer so that the operation and reading of the measuring instruments can be remotely controlled from the measuring chamber. (Air Pollut. Abstr.)

Ambient water quality criteria for polycyclic aromatic hydrocarbons (PAHs)

Energy Technology Data Exchange (ETDEWEB)

Nagpal, N.K.

1993-08-13

Ambient water quality criteria are established for polyaromatic hydrocarbons (PAH) in British Columbia. Major sources of PAH in the atmosphere and aquatic environments include, for the atmosphere, forest and prairie fires, agricultural burning, refuse burning, enclosed incineration, and heating and power, and for the aquatic environment, petroleum spillage, atmospheric deposition, wastewaters, surface land runoff, and biosynthesis. Details are presented of PAH and their characteristics, forms and transformations, occurrence in the environment, drinking water concerns, aquatic life concerns, wildlife concerns, livestock water supply concerns, and irrigation concerns. Application of criteria for aquatic life is discussed including phototoxic vs long term criteria, assessment of existing water quality, setting water quality objectives, and PAH levels in smoked fish. 221 refs., 5 figs., 30 tabs.

Study of self-assembled triethoxysilane thin films made by casting neat reagents in ambient atmosphere

International Nuclear Information System (INIS)

Yang Yongan; Bittner, Alexander M.; Baldelli, Steve; Kern, Klaus

2008-01-01

We studied four trialkoxysilane thin films, fabricated via self-assembly by casting neat silane reagents onto hydrophilic SiO x /Si substrates in the ambient. This drop-casting method is simple, yet rarely studied for the production of silane self-assembled monolayers (SAMs). Various ex-situ techniques were utilized to systematically characterize the growth process: Ellipsometry measurements can monitor the evolution of film thickness with silanization time; water droplet contact angle measurements reveal the wettability; the change of surface morphology was followed by Atomic Force Microscopy; the chemical identity of the films was verified by Infrared-Visible Sum Frequency Generation spectroscopy. We show that the shorter carbon chain (propyl-) or branched (2-(diphenylphosphino)ethyl-) silane SAMs exhibit poor ordering. In contrast, longer carbon chain (octadecyl and decyl) silanes form relatively ordered monolayers. The growth of the latter two cases shows Langmuir-like kinetics and a transition process from lying-down to standing-up geometry with increasing coverage

An Evaluation of Uncertainty Associated to Analytical Measurements of Selected Polycyclic Aromatic Compounds in Ambient Air

International Nuclear Information System (INIS)

Barrado, A. I.; Garcia, S.; Perez, R. M.

2013-01-01

This paper presents an evaluation of uncertainty associated to analytical measurement of eighteen polycyclic aromatic compounds (PACs) in ambient air by liquid chromatography with fluorescence detection (HPLC/FD). The study was focused on analyses of PM 1 0, PM 2 .5 and gas phase fractions. Main analytical uncertainty was estimated for eleven polycyclic aromatic hydrocarbons (PAHs), four nitro polycyclic aromatic hydrocarbons (nitro-PAHs) and two hydroxy polycyclic aromatic hydrocarbons (OH-PAHs) based on the analytical determination, reference material analysis and extraction step. Main contributions reached 15-30% and came from extraction process of real ambient samples, being those for nitro- PAHs the highest (20-30%). Range and mean concentration of PAC mass concentrations measured in gas phase and PM 1 0/PM 2 .5 particle fractions during a full year are also presented. Concentrations of OH-PAHs were about 2-4 orders of magnitude lower than their parent PAHs and comparable to those sparsely reported in literature. (Author)

Corona discharge experiments in admixtures of N2 and CH4: a laboratory simulation of Titan's atmosphere

OpenAIRE

Horvath, G.; Skalny, J. D.; Mason, N. J.; Klas, M.; Zahoran, M.; Vladoiu, R.; Manole, M.

2009-01-01

A positive corona discharge fed by a N2:CH4 mixture (98:2) at atmospheric pressure and ambient temperature has been studied as a laboratory mimic of the chemical processes occurring in the atmosphere of Titan, Saturn's largest moon. In-situ measurements of UV and IR transmission spectra within the discharge have shown that the main chemical product is C2H2, produced by dissociation of CH4, with small but significant traces of ethane and HCN, all species that have been detected in Titan's atmo...

Remote measurement of atmospheric pollutants with laser techniques

Energy Technology Data Exchange (ETDEWEB)

Corio, W; Querzola, B; Zanzottera, E

1979-03-01

Laser techniques for the remote sensing of atmospheric pollutants are reviewed, with attention given to lidars based on Rayleigh and Mie scattering, the Raman effect, or fluorescent scattering. Emphasis is placed on differential absorption lidars, which rely on Rayleigh or Mie scattering for measurements made in the IR or in the visible-UV range, respectively. A comprehensive air pollution monitoring program based on differential absorption lidars, together with systems using fluorescent backscattering and absorption measurements with topographic backscattering, is described.

L-Band Radiometers Measuring Salinity From Space: Atmospheric Propagation Effects

DEFF Research Database (Denmark)

Skou, Niels; Hofman-Bang, Dorthe

2005-01-01

Microwave radiometers can measure sea surface salinity from space using L-band frequencies around 1.4 GHz. However, requirements to the accuracy of the measurements, in order to be satisfactory for the user, are so stringent that the influence of the intervening atmosphere cannot be neglected...

Simultaneous temperature measurement of ionospheric plasma and neutral atmosphere with K-10-11 rocket

International Nuclear Information System (INIS)

Murasato, Yukio; Kaneko, Osamu; Sasaki, Susumu; Kawashima, Nobuki; Kibune, Tadashi.

1976-01-01

Ion temperature and neutral atmospheric temperature in lower ionospheric layer were measured by the ''Shadow Method'', which has been developed and improved by the authors. The principle of the method, which utilizes the fact that the shadow due to the reduction of density of medium behind on obstacle depends upon the flow velocity and the temperature of the medium, is briefly explained together with the apparatus used for the measurement. A pair of the Langmuir probes with the interval of 44 mm was used for the measurement of ion temperature. For the measurement of the neutral atmospheric temperature, its density was measured with the ionization gauge. The measuring system was mounted on the K-10-11 rocket, and launched from KSC at 2 p.m., September 24, 1975. Although the rocket itself reached its highest altitude of 196 km, the temperature measurement was performed between the altitude of 80 km and 140 km. The measured temperatures of ions, neutral atmosphere, and electrons are presented as the functions of altitude. It is confirmed that the temperatures of ions and neutral atmosphere are lower than that of electrons in that range of altitude. (Aoki, K.)

Three Mile Island ambient-air-temperature sensor measurements

International Nuclear Information System (INIS)

Fryer, M.O.

1983-01-01

Data from the ambient-air-temperature sensors in Three Mile Island-Unit 2 (TMI-2) reactor containment building are analyzed. The data were for the period of the hydrogen burn that was part of the TMI-2 accident. From the temperature data, limits are placed on the duration of the hydrogen burn

Measurement of the atmospheric muon charge ratio with the OPERA detector

CERN Document Server

Agafonova, N.; Aoki, S.; Ariga, A.; Ariga, T.; Autiero, D.; Badertscher, A.; Bagulya, A.; Bertolin, A.; Besnier, M.; Bick, D.; Boyarkin, V.; Bozza, C.; Brugiere, T.; Brugnera, R.; Brunetti, G.; Buontempo, S.; Cazes, A.; Chaussard, L.; Chernyavsky, M.; Chiarella, V.; Chon-Sen, N.; Chukanov, A.; Cozzi, M.; D'Amato, G.; Dal Corso, F.; D'Ambrosio, N.; De Lellis, G.; Declais, Y.; De Serio, M.; Di Capua, F.; Di Ferdinando, D.; Di Giovanni, A.; Di Marco, N.; Dmitrievski, S.; Dracos, M.; Duchesneau, D.; Dusini, S.; Ebert, J.; Egorov, O.; Enikeev, R.; Ereditato, A.; Esposito, L.S.; Favier, J.; Felici, G.; Ferber, T.; Fini, R.; Frekers, D.; Fukuda, T.; Fukushima, C.; Galkin, V.I.; Garfagnini, A.; Giacomelli, G.; Giorgini, M.; Goellnitz, C.; Goldberg, J.; Golubkov, D.; Goncharova, L.; Gornushkin, Y.; Grella, G.; Grianti, F.; Guler, M.; Gustavino, C.; Hagner, C.; Hamada, K.; Hara, T.; Hierholzer, M.; Hoshino, K.; Ieva, M.; Jakovcic, K.; Jollet, C.; Juget, F.; Kazuyama, M.; Kim, S.H.; Kimura, M.; Klicek, B.; Knuesel, J.; Kodama, K.; Komatsu, M.; Kose, U.; Kreslo, I.; Kubota, H.; Lazzaro, C.; Lenkeit, J.; Ljubicic, A.; Longhin, A.; Lutter, G.; Malgin, A.; Mandrioli, G.; Marotta, A.; Marteau, J.; Matsuo, T.; Matveev, V.; Mauri, N.; Medinaceli, E.; Meisel, F.; Meregaglia, A.; Migliozzi, P.; Mikado, S.; Miyamoto, S.; Monacelli, P.; Morishima, K.; Moser, U.; Muciaccia, M.T.; Naganawa, N.; Naka, T.; Nakamura, M.; Nakano, T.; Naumov, D.; Nikitina, V.; Niwa, K.; Nonoyama, Y.; Ogawa, S.; Olchevski, A.; Oldorf, C.; Orlova, G.; Osedlo, V.; Paniccia, M.; Paoloni, A.; Park, B.D.; Park, I.G.; Pastore, A.; Patrizii, L.; Pennacchio, E.; Pessard, H.; Pilipenko, V.; Pistillo, C.; Policastro, G.; Polukhina, N.; Pozzato, M.; Pretzl, K.; Publichenko, P.; Pupilli, F.; Rescigno, R.; Roganova, T.; Rokujo, H.; Romano, G.; Rosa, G.; Rostovtseva, I.; Rubbia, A.; Russo, A.; Ryasny, V.; Ryazhskaya, O.; Sato, O.; Sato, Y.; Schembri, A.; Schmidt Parzefall, W.; Schroeder, H.; Scotto Lavina, L.; Sheshukov, A.; Shibuya, H.; Simone, S.; Sioli, M.; Sirignano, C.; Sirri, G.; Song, J.S.; Spinetti, M.; Stanco, L.; Starkov, N.; Stipcevic, M.; Strauss, T.; Strolin, P.; Takahashi, S.; Tenti, M.; Terranova, F.; Tezuka, I.; Tioukov, V.; Tolun, P.; Tran, T.; Tufanli, S.; Vilain, P.; Vladimirov, M.; Votano, L.; Vuilleumier, J.L.; Wilquet, G.; Wonsak, B.; Yakushev, V.; Yoon, C.S.; Yoshioka, T.; Yoshida, J.; Zaitsev, Y.; Zemskova, S.; Zghiche, A.; Zimmermann, R.

2010-01-01

The OPERA detector at the Gran Sasso underground laboratory (LNGS) was used to measure the atmospheric muon charge ratio in the TeV energy region. We analyzed 403069 atmospheric muons corresponding to 113.4 days of livetime during the 2008 CNGS run. We computed separately the muon charge ratio for single and for multiple muon events in order to select different energy regions of the primary cosmic ray spectrum and to test the charge ratio dependence on the primary composition. The measured charge ratio values were corrected taking into account the charge-misidentification errors. Data have also been grouped in five bins of the "vertical surface energy". A fit to a simplified model of muon production in the atmosphere allowed the determination of the pion and kaon charge ratios weighted by the cosmic ray energy spectrum.

Variations of aerosol size distribution, chemical composition and optical properties from roadside to ambient environment: A case study in Hong Kong, China

Science.gov (United States)

Zhang, Qian; Ning, Zhi; Shen, Zhenxing; Li, Guoliang; Zhang, Junke; Lei, Yali; Xu, Hongmei; Sun, Jian; Zhang, Leiming; Westerdahl, Dane; Gali, Nirmal Kumar; Gong, Xuesong

2017-10-01

This study investigated the ;roadside-to-ambient; evolution of particle physicochemical and optical properties in typical urban atmospheres of Hong Kong through collection of chemically-resolved PM2.5 data and PM2.5 size distribution at a roadside and an ambient site. Roadside particle size distribution showed typical peaks in the nuclei mode (30-40 nm) while ambient measurements peaked in the Aitken mode (50-70 nm), revealing possible condensation and coagulation growth of freshly emitted particles during aging processes. Much higher levels of anthropogenic chemical components, i.e. nitrate, sulfate, ammonium, organic carbon (OC) and elemental carbon (EC), but lower levels of OC/EC and secondary inorganic aerosols (SIA)/EC ratios appeared in roadside than ambient particles. The high OC/EC and SIA/EC ratios in ambient particles implied high contributions from secondary aerosols. Black carbon (BC), a strong light absorbing material, showed large variations in optical properties when mixed with other inorganic and organic components. Particle-bound polycyclic aromatic hydrocarbons (p-PAHs), an indicator of brown carbon (BrC), showed significant UV-absorbing ability. The average BC and p-PAHs concentrations were 3.8 and 87.6 ng m-3, respectively, at the roadside, but were only 1.5 and 18.1 ng m-3 at the ambient site, suggesting BC and p-PAHs concentrations heavily driven by traffic emissions. In contrast, PM2.5 UV light absorption coefficients (babs-BrC,370nm) at the ambient site (4.2 Mm-1) and at the roadside site (4.1 Mm-1) were similar, emphasizing that particle aging processes enhanced UV light-absorbing properties, a conclusion that was also supported by the finding that the Absorption Ångström coefficient (AAC) value at UV wavelengths (AAC_UV band) at the ambient site were ∼1.7 times higher than that at the roadside. Both aqueous reaction and photochemically produced secondary organic aerosol (SOA) for ambient aerosols contributed to the peak values of babs

First Measurements of Ambient Total Gaseous Mercury (TGM at the EvK2CNR Pyramid Observatory in Nepal

Directory of Open Access Journals (Sweden)

Gratz L. E.

2013-04-01

Full Text Available As part of the Global Mercury Observation System (GMOS project, a global-scale network of ground-based atmospheric monitoring sites is being developed with the objective of expanding the global coverage of atmospheric mercury (Hg measurements and improving our understanding of global atmospheric Hg transport. An important addition to the GMOS monitorng network has been the high altitude EvK2CNR Pyramid Observatory, located at an elevation of 5,050 meters a.s.l. in the eastern Himalaya Mountains of Nepal. Monitoring of total gaseous mercury (TGM using the Tekran 2537A Mercury Vapor Analyzer began at the EvK2CNR Pyramid Observatory in November 2011. From 17 November 2011 to 23 April 2012, the mean concentration of TGM at the Pyramid was 1.2 ng m−3. A range of concentrations from 0.7 to 2.6 ng m−3 has been observed. These are the first reported measurements of atmospheric Hg in Nepal, and currently this is the highest altitude monitoring station for atmospheric Hg in the world. It is anticipated that these high quality measurements, in combination with the other continuous atmospheric measurments being collected at the Pyramid station, will help to further our understanding of Hg concentrations in the free troposphere and the transport of atmospheric Hg on the global scale.

Metrological traceability of carbon dioxide measurements in atmosphere and seawater

International Nuclear Information System (INIS)

Rolle, F; Pessana, E; Sega, M

2017-01-01

The accurate determination of gaseous pollutants is fundamental for the monitoring of the trends of these analytes in the environment and the application of the metrological concepts to this field is necessary to assure the reliability of the measurement results. In this work, an overview of the activity carried out at Istituto Nazionale di Ricerca Metrologica to establish the metrological traceability of the measurements of gaseous atmospheric pollutants, in particular of carbon dioxide (CO 2 ), is presented. Two primary methods, the gravimetry and the dynamic dilution, are used for the preparation of reference standards for composition which can be used to calibrate sensors and analytical instrumentation. At present, research is carried out to lower the measurement uncertainties of the primary gas mixtures and to extend their application to the oceanic field. The reason of such investigation is due to the evidence of the changes occurring in seawater carbonate chemistry, connected to the rising level of CO 2 in the atmosphere. The well established activity to assure the metrological traceability of CO 2 in the atmosphere will be applied to the determination of CO 2 in seawater, by developing suitable reference materials for calibration and control of the sensors during their routine use. (paper)

Effect of Atmospheric Conditions on LIBS Spectra

Science.gov (United States)

Effenberger, Andrew J.; Scott, Jill R.

2010-01-01

Laser-induced breakdown spectroscopy (LIBS) is typically performed at ambient Earth atmospheric conditions. However, interest in LIBS in other atmospheric conditions has increased in recent years, especially for use in space exploration (e.g., Mars and Lunar) or to improve resolution for isotopic signatures. This review focuses on what has been reported about the performance of LIBS in reduced pressure environments as well as in various gases other than air. PMID:22399914

Comparison of ambient aerosol extinction coefficients obtained from in-situ, MAX-DOAS and LIDAR measurements at Cabauw

NARCIS (Netherlands)

Zieger, P.; Weingartner, E.; Henzing, J.; Moerman, M.; Leeuw, G. de; Mikkilä, J.; Ehn, M.; Petäjä, T.; Clémer, K.; Roozendael, M. van; Yilmaz, S.; Frieß, U.; Irie, H.; Wagner, T.; Shaiganfar, R.; Beirle, S.; Apituley, A.; Wilson, K.; Baltensperger, U.

2011-01-01

In the field, aerosol in-situ measurements are often performed under dry conditions (relative humidity RH<30-40%). Since ambient aerosol particles experience hygroscopic growth at enhanced RH, their microphysical and optical properties especially the aerosol light scattering are also strongly

New insights to the use of ethanol in automotive fuels: a stable isotopic tracer for fossil- and bio-fuel combustion inputs to the atmosphere.

Science.gov (United States)

Giebel, Brian M; Swart, Peter K; Riemer, Daniel D

2011-08-01

Ethanol is currently receiving increased attention because of its use as a biofuel or fuel additive and because of its influence on air quality. We used stable isotopic ratio measurements of (13)C/(12)C in ethanol emitted from vehicles and a small group of tropical plants to establish ethanol's δ(13)C end-member signatures. Ethanol emitted in exhaust is distinctly different from that emitted by tropical plants and can serve as a unique stable isotopic tracer for transportation-related inputs to the atmosphere. Ethanol's unique isotopic signature in fuel is related to corn, a C4 plant and the primary source of ethanol in the U.S. We estimated a kinetic isotope effect (KIE) for ethanol's oxidative loss in the atmosphere and used previous assumptions with respect to the fractionation that may occur during wet and dry deposition. A small number of interpretive model calculations were used for source apportionment of ethanol and to understand the associated effects resulting from atmospheric removal. The models incorporated our end-member signatures and ambient measurements of ethanol, known or estimated source strengths and removal magnitudes, and estimated KIEs associated with atmospheric removal processes for ethanol. We compared transportation-related ethanol signatures to those from biogenic sources and used a set of ambient measurements to apportion each source contribution in Miami, Florida-a moderately polluted, but well ventilated urban location.

Correlation-study about the ambient dose rate and the weather conditions

Science.gov (United States)

Furuya, Masato; Hatano, Yuko; Aoyama, Tomoo; Igarashi, Yasuhito; Kita, Kazuyuki; Ishizuka, Masahide

2016-04-01

The long-term radiation risks are believed to be heavily affected by the resuspension process. We therefore focus on the surface-atmosphere exchange process of released radioactive materials in this study. Radioactive materials were deposited on the soil and float in the air, and such complicated process are influenced by the weather conditions deeply. We need to reveal the correlation between the weather conditions and the ambient dose rate. In this study, we study the correlation between the weather conditions and the ambient dose rate with the correction of the decrease due to the radioactive decay. We found that there is a negative correlation between the ambient dose rate and the soil water content by the correlation coefficient. Using this result, we reconstruct the ambient dose rate from the weather conditions by the multiple regression analysis and found that the reconstructed data agree with the observation very well. Using Kalman filter, which can be sequentially updates the state estimate, we obtained such a good agreement.

Observations of linear dependence between sulfate and nitrate in atmospheric particles

Science.gov (United States)

Kong, Lingdong; Yang, Yiwei; Zhang, Shuanqin; Zhao, Xi; Du, Huanhuan; Fu, Hongbo; Zhang, Shicheng; Cheng, Tiantao; Yang, Xin; Chen, Jianmin; Wu, Dui; Shen, Jiandong; Hong, Shengmao; Jiao, Li

2014-01-01

Hourly measurements of water-soluble inorganic ionic species in ambient atmospheric particles were conducted at Shanghai, Hangzhou, and Guangzhou sampling sites in China during the period of 2009-2011. The relation between sulfate and nitrate in particulate matter (PM10 and PM2.5) was examined based on these measurements. Results showed that the mass fraction of sulfate was strongly negatively correlated with that of nitrate in atmospheric particles on most of the sampling days, especially when sulfate and nitrate made up the vast majority of the total soluble anions and cations (Na+, K+, Ca2+, and Mg2+) made a small contribution to the total water-soluble ions, revealing that the formation mechanisms of sulfate and nitrate in the atmosphere are highly correlated, and there exists a significant negative correlation trend between sulfate and nitrate mass fractions in the atmospheric particles. We found that local meteorological conditions presented opposite influences on the mass fractions of sulfate and nitrate. Further analysis indicated that the two mass fractions were modulated by the neutralizing level of atmospheric aerosols, and the negative correlation could be found in acidic atmospheric particles. Strong negative correlation was usually observed on clear days, hazy days, foggy days, and respirable particulate air pollution days, whereas poor negative correlation was often observed during cloud, rain, snow, dust storm, and suspended dust events. The results can help to better understand the formation mechanisms of atmospheric sulfate and nitrate during air pollution episodes and to better explain field results of atmospheric chemistry concerning sulfate and nitrate.

A comparative study of carbon plasma emission in methane and argon atmospheres

Science.gov (United States)

Yousfi, H.; Abdelli-Messaci, S.; Ouamerali, O.; Dekhira, A.

2018-04-01

The interaction between laser produced plasma (LPP) and an ambient gas is largely investigated by Optical Emission Spectroscopy (OES). The analysis of carbon plasma produced by an excimer KrF laser was performed under controlled atmospheres of methane and argon. For each ambient gas, the features of produced species have been highlighted. Using the time of flight (TOF) analysis, we have observed that the C and C2 exhibit a triple and a double peaks respectively in argon atmosphere in contrast to the methane atmosphere. The evolution of the first peaks of C and C2 follows the plasma expansion, whereas the second peaks move backward, undergoing reflected shocks. It was found that the translational temperature, obtained by Shifted Maxwell Boltzmann distribution function is strongly affected by the nature of ambient gas. The dissociation of CH4 by electronic impact presents the principal approach for explaining the emission of CH radical in reactive plasma. Some chemical reactions have been proposed in order to explain the formation process of molecular species.

Temporal evolution of main ambient PM2. 5 sources in Santiago, Chile, from 1998 to 2012

Science.gov (United States)

Barraza, Francisco; Lambert, Fabrice; Jorquera, Héctor; María Villalobos, Ana; Gallardo, Laura

2017-08-01

The inhabitants of Santiago, Chile have been exposed to harmful levels of air pollutants for decades. The city's poor air quality is a result of steady economic growth, and stable atmospheric conditions adverse to mixing and ventilation that favor the formation of oxidants and secondary aerosols. Identifying and quantifying the sources that contribute to the ambient levels of pollutants is key for designing adequate mitigation measures. Estimating the evolution of source contributions to ambient pollution levels is also paramount to evaluating the effectiveness of pollution reduction measures that have been implemented in recent decades. Here, we quantify the main sources that have contributed to fine particulate matter (PM2. 5) between April 1998 and August 2012 in downtown Santiago by using two different source-receptor models (PMF 5.0 and UNMIX 6.0) that were applied to elemental measurements of 1243 24 h filter samples of ambient PM2.5. PMF resolved six sources that contributed to ambient PM2. 5, with UNMIX producing similar results: motor vehicles (37.3 ± 1.1 %), industrial sources (18.5 ± 1.3 %), copper smelters (14.4 ± 0.8 %), wood burning (12.3 ± 1.0 %), coastal sources (9.5 ± 0.7 %) and urban dust (3.0 ± 1.2 %). Our results show that over the 15 years analyzed here, four of the resolved sources significantly decreased [95 % confidence interval]: motor vehicles 21.3 % [2.6, 36.5], industrial sources 39.3 % [28.6, 48.4], copper smelters 81.5 % [75.5, 85.9], and coastal sources 58.9 % [38.5, 72.5], while wood burning did not significantly change and urban dust increased by 72 % [48.9, 99.9]. These changes are consistent with emission reduction measures, such as improved vehicle emission standards, cleaner smelting technology, introduction of low-sulfur diesel for vehicles and natural gas for industrial processes, public transport improvements, etc. However, it is also apparent that the mitigation expected from the above regulations has been partially

Atmospheric heavy metals and Arsenic in China: Situation, sources and control policies

Science.gov (United States)

Duan, Jingchun; Tan, Jihua

2013-08-01

In recent years, heavy metal pollution accidents were reported frequently in China. The atmospheric heavy metal pollution is drawing all aspects of attention. This paper summarizes the recent research results from our studies and previous studies in recent years in China. The level, temporal variation, seasonal variation and size distribution of the heavy metals of atmospheric Lead(Pb), Vanadium(V), Manganese(Mn), Nickel(Ni), Chromium(Cr), Cadmium(Cd), Copper(Cu), Zinc(Zn) and Arsenic(As) were characterized in China. The emission characteristics and sources of atmospheric heavy metals and As in China were reviewed. Coal burning, iron and steel industry and vehicle emission are important sources in China. Control policies and effects in China were reviewed including emission standards, ambient air quality standards, phase out of leaded gasoline and so on, and further works for atmospheric heavy metals control were suggested. The comprehensive heavy metals pollution control measures and suggestions were put forward based on the summarization of the development and experience of the atmospheric heavy metal pollution control abroad.

A comparison of GC-FID and PTR-MS toluene measurements in ambient air under conditions of enhanced monoterpene loading

Directory of Open Access Journals (Sweden)

J. L. Ambrose

2010-07-01

Full Text Available Toluene was measured using both a gas chromatographic system (GC, with a flame ionization detector (FID, and a proton transfer reaction-mass spectrometer (PTR-MS at the AIRMAP atmospheric monitoring station Thompson Farm (THF in rural Durham, NH during the summer of 2004. Simultaneous measurements of monoterpenes, including α- and β-pinene, camphene, Δ ³-carene, and d-limonene, by GC-FID demonstrated large enhancements in monoterpene mixing ratios relative to toluene, with median and maximum enhancement ratios of ~2 and ~30, respectively. A detailed comparison between the GC-FID and PTR-MS toluene measurements was conducted to test the specificity of PTR-MS for atmospheric toluene measurements under conditions often dominated by biogenic emissions. We derived quantitative estimates of potential interferences in the PTR-MS toluene measurements related to sampling and analysis of monoterpenes, including fragmentation of the monoterpenes and some of their primary carbonyl oxidation products via reactions with H₃O⁺, O₂⁺ and NO⁺ in the PTR-MS drift tube. The PTR-MS and GC-FID toluene measurements were in good quantitative agreement and the two systems tracked one another well from the instrumental limits of detection to maximum mixing ratios of ~0.5 ppbv. A correlation plot of the PTR-MS versus GC-FID toluene measurements was described by the least squares regression equation y=(1.13± 0.02x−(0.008±0.003 ppbv, suggesting a small ~13% positive bias in the PTR-MS measurements. The bias corresponded with a ~0.055 ppbv difference at the highest measured toluene level. The two systems agreed quantitatively within the combined 1σ measurement precisions for 60% of the measurements. Discrepancies in the measured mixing ratios were not well correlated with enhancements in the monoterpenes. Better quantitative agreement between the two systems was obtained by

Modification, calibration, and performance of the Ultra-High Sensitivity Aerosol Spectrometer for particle size distribution and volatility measurements during the Atmospheric Tomography Mission (ATom airborne campaign

Directory of Open Access Journals (Sweden)

A. Kupc

2018-01-01

Full Text Available Atmospheric aerosol is a key component of the chemistry and climate of the Earth's atmosphere. Accurate measurement of the concentration of atmospheric particles as a function of their size is fundamental to investigations of particle microphysics, optical characteristics, and chemical processes. We describe the modification, calibration, and performance of two commercially available, Ultra-High Sensitivity Aerosol Spectrometers (UHSASs as used on the NASA DC-8 aircraft during the Atmospheric Tomography Mission (ATom. To avoid sample flow issues related to pressure variations during aircraft altitude changes, we installed a laminar flow meter on each instrument to measure sample flow directly at the inlet as well as flow controllers to maintain constant volumetric sheath flows. In addition, we added a compact thermodenuder operating at 300 °C to the inlet line of one of the instruments. With these modifications, the instruments are capable of making accurate (ranging from 7 % for Dp < 0.07 µm to 1 % for Dp > 0.13 µm, precise (< ±1.2 %, and continuous (1 Hz measurements of size-resolved particle number concentration over the diameter range of 0.063–1.0 µm at ambient pressures of > 1000 to 225 hPa, while simultaneously providing information on particle volatility.We assessed the effect of uncertainty in the refractive index (n of ambient particles that are sized by the UHSAS assuming the refractive index of ammonium sulfate (n =  1.52. For calibration particles with n between 1.44 and 1.58, the UHSAS diameter varies by +4/−10 % relative to ammonium sulfate. This diameter uncertainty associated with the range of refractive indices (i.e., particle composition translates to aerosol surface area and volume uncertainties of +8.4/−17.8 and +12.4/−27.5 %, respectively. In addition to sizing uncertainty, low counting statistics can lead to uncertainties of < 20 % for aerosol surface area and < 30�

Composition and properties of atmospheric particles in the eastern Atlantic and impacts on gas phase uptake rates

Directory of Open Access Journals (Sweden)

G. McFiggans

2009-12-01

Full Text Available Marine aerosol composition continues to represent a large source of uncertainty in the study of climate and atmospheric chemistry. In addition to their physical size and chemical composition, hygroscopicity plays a significant role, increasing the particles' surface areas and scattering potential. Simultaneous aerosol measurements were performed on board the RRS Discovery and at the Cape Verde atmospheric observatory during the Aerosol Composition and Modelling in the Marine Environment (ACMME and Reactive Halogens in the Marine Boundary Layer (RHAMBLE experiments. These included online measurements of number and dry size and bulk collection for offline analysis of aqueous ions. In addition, the measurements on board the Discovery included online measurements of composition using an Aerodyne Aerosol Mass Spectrometer, optical absorption using a Multi Angle Absorption Photometer, ambient humidity size distribution measurements using a humidified differential mobility particle sizer (DMPS and optical particle counter (OPC and hygroscopicity measurements with a hygroscopicity tandem differential mobility analyser (HTDMA.

Good agreement between platforms in terms of the sea salt (ss and non sea salt (nss modes was found during the period when the Discovery was in close proximity to Cape Verde and showed a composition consistent with remote marine air. As the Discovery approached the African coast, the aerosol showed signs of continental influence such as an increase in particle number, optical absorption, enhancement of the nss mode and dust particles. The Cape Verde site was free of this influence during this period. Chloride and bromide showed concentrations with significant deviations from seawater relative to sodium, indicating that atmospheric halogen processing (and/or acid displacement for chloride had taken place. The time dependent ambient size distribution was synthesised using humidified DMPS and OPC data, corrected to ambient

Control of emissions from stationary combustion sources: Pollutant detection and behavior in the atmosphere

International Nuclear Information System (INIS)

Licht, W.; Engel, A.J.; Slater, S.M.

1979-01-01

Stationary combustion resources continue to be significant sources of NOx and SOx pollutants in the ambient atmosphere. This volume considers four problem areas: (1) control of emissions from stationary combustion sources, particularly SOx and NOx (2) pollutant behavior in the atmosphere (3) advances in air pollution analysis and (4) air quality management. Topics of interest include carbon slurries for sulfur dioxide abatement, mass transfer in the Kellogg-Weir air quality control system, oxidation/inhibition of sulfite ion in aqueous solution, some micrometeorological methods of measuring dry deposition rates, Spanish moss as an indicator of airborne metal contamination, and air quality impacts from future electric power generation in Texas

Effects of initiating anaerobic digestion of layer-hen poultry dung at sub-atmospheric pressure

OpenAIRE

Ngumah, Chima C.; Ogbulie, Jude N.; Orji, Justina C.; Amadi, Ekperechi S.

2013-01-01

This study investigated the effects of initiating anaerobic digestion (AD) of dry layer-hen poultry dung at the sub-atmospheric pressure of -30 cmHg on biodegradation, biogasification, and biomethanation. The setup was performed as a batch process at an average ambient temperature of 29±2 ºC and a retention time of 15 days. Comparisons were made with two other experiments which were both begun at ambient atmospheric pressure; one was inoculated with digestate from a previous layer-hen dung AD...

Measuring techniques of minute amounts of NO/sub x/ present in the atmosphere

Energy Technology Data Exchange (ETDEWEB)

Futsuhara, N

1974-06-01

A comparison was made between the chemiluminescence measuring method for nitrogen oxides and the automatic Saltzman analyzer method. The reaction between nitrite oxide and ozone is allowed to proceed in reduced pressure or under ordinary pressure. The light emitted by the progress of the reaction is detected with a photoelectron multiplier and used to determine the NO concentration. Nitrogen dioxide is converted into NO before determination. This method is quick in response and highly sensitive. Also, the experimental data are little affected by the presence of various gases usually present in the ambient atmosphere. The Saltzman method makes use of the coloration of sulfanyl acid or N-(1-naphthyl)ethylenediamine by nitric ion, which is formed by the reaction between water and NO/sub 2/. By this method, NO is converted to NO/sub 2/ by oxidation with potassium permanganate if NO is to be determined. The disadvantage of this method is that the data are not available until at least 1 hour after the determination. The permeation membrane method was examined for the preparation of standard gases to be used for the determination. This method has various advantages over the permeation tube method. The data obtained by the Saltzman method were compared with those obtained by the chemiluminescence method with the aid of the standard gases prepared by the permeation membrane method.

Solid Sampling with a Diode Laser for Portable Ambient Mass Spectrometry.

Science.gov (United States)

Yung, Yeni P; Wickramasinghe, Raveendra; Vaikkinen, Anu; Kauppila, Tiina J; Veryovkin, Igor V; Hanley, Luke

2017-07-18

A hand-held diode laser is implemented for solid sampling in portable ambient mass spectrometry (MS). Specifically, a pseudocontinuous wave battery-powered surgical laser diode is employed for portable laser diode thermal desorption (LDTD) at 940 nm and compared with nanosecond pulsed laser ablation at 2940 nm. Postionization is achieved in both cases using atmospheric pressure photoionization (APPI). The laser ablation atmospheric pressure photoionization (LAAPPI) and LDTD-APPI mass spectra of sage leaves (Salvia officinalis) using a field-deployable quadrupole ion trap MS display many similar ion peaks, as do the mass spectra of membrane grown biofilms of Pseudomonas aeruginosa. These results indicate that LDTD-APPI method should be useful for in-field sampling of plant and microbial communities, for example, by portable ambient MS. The feasibility of many portable MS applications is facilitated by the availability of relatively low cost, portable, battery-powered diode lasers. LDTD could also be coupled with plasma- or electrospray-based ionization for the analysis of a variety of solid samples.

Composition and oxidation state of sulfur in atmospheric particulate matter

Directory of Open Access Journals (Sweden)

A. F. Longo

2016-10-01

Full Text Available The chemical and physical speciation of atmospheric sulfur was investigated in ambient aerosol samples using a combination of sulfur near-edge x-ray fluorescence spectroscopy (S-NEXFS and X-ray fluorescence (XRF microscopy. These techniques were used to determine the composition and oxidation state of sulfur in common primary emission sources and ambient particulate matter collected from the greater Atlanta area. Ambient particulate matter samples contained two oxidation states: S0 and S+VI. Ninety-five percent of the individual aerosol particles (> 1 µm analyzed contain S0. Linear combination fitting revealed that S+VI in ambient aerosol was dominated by ammonium sulfate as well as metal sulfates. The finding of metal sulfates provides further evidence for acidic reactions that solubilize metals, such as iron, during atmospheric transport. Emission sources, including biomass burning, coal fly ash, gasoline, diesel, volcanic ash, and aerosolized Atlanta soil, and the commercially available bacterium Bacillus subtilis, contained only S+VI. A commercially available Azotobacter vinelandii sample contained approximately equal proportions of S0 and S+VI. S0 in individual aerosol particles most likely originates from primary emission sources, such as aerosolized bacteria or incomplete combustion.

Ambient air quality observations in the Athabasca oil sands region

International Nuclear Information System (INIS)

1996-01-01

Both Syncrude and Suncor have plans to develop new oil sands leases and to increase crude oil and bitumen recovery in the Athabasca oil sands region. In recognition of the effects that this will have on the environment, Suncor has proposed modifications to reduce SO 2 emissions to the atmosphere, while Syncrude plans to develop additional ambient air quality, sulphur deposition and biomonitoring programs. This report discussed the ambient air quality monitoring that was undertaken in the Fort McMurray-Fort McKay airshed. Twelve continuous ambient air quality stations and 76 passive monitoring stations are maintained in the region. Environment Canada maintains eight precipitation monitoring stations in northern Alberta and Saskatchewan. Source characterization, ambient air quality and meteorology observations, air quality monitoring, and air quality data from continuous sulphur dioxide, hydrogen sulphide, nitrogen oxides, ozone, carbon monoxide, hydrocarbon, acid rain and particulates analyzers were reviewed. The documentation of all computer files used for the analysis of the air quality data is discussed in the Appendix. 47 refs., 39 tabs., 53 figs

Direct measurement of electron density in microdischarge at atmospheric pressure by Stark broadening

International Nuclear Information System (INIS)

Dong Lifang; Ran Junxia; Mao Zhiguo

2005-01-01

We present a method and results for measurement of electron density in atmospheric-pressure dielectric barrier discharge. The electron density of microdischarge in atmospheric pressure argon is measured by using the spectral line profile method. The asymmetrical deconvolution is used to obtain Stark broadening. The results show that the electron density in single filamentary microdischarge at atmospheric pressure argon is 3.05x10 15 cm -3 if the electron temperature is 10,000 K. The result is in good agreement with the simulation. The electron density in dielectric barrier discharge increases with the increase of applied voltage

Does ambient noise or hypobaric atmosphere influence olfactory and gustatory function?

Science.gov (United States)

Rahne, Torsten; Köppke, Robert; Nehring, Michael; Plontke, Stefan K; Fischer, Hans-Georg

2018-01-01

Multidimensional food perception is based mainly on gustatory and olfactory function. Recent research has demonstrated that hypobaric pressure impairs gustatory function and that background noise or distracting auditory stimulation impairs olfactory function. Using a hypobaric chamber, the odor identification, discrimination, and thresholds as well as taste identification and threshold scores were measured in 16 healthy male volunteers under normal and hypobaric (6380 ft) conditions using clinically validated tests. In both conditions, background noise was either canceled out or replaced by white noise presentation (70 dB sound pressure level). Olfactory sensitivity for n-butanol and gustatory sensitivity were impaired in a hypobaric atmosphere. White noise did not influence the odor test results. White noise stimulation impaired sensitivity for sour and sweet but not for bitter or salty tastants. We conclude that hypobaric or noisy environments could impair gustatory and olfactory sensitivity selectively for particular tastants and odorants.

Measurement of the atmospheric muon charge ratio with the OPERA detector

International Nuclear Information System (INIS)

Agafonova, N.; Boyarkin, V.; Enikeev, R.; Malgin, A.; Matveev, V.; Ryasny, V.; Ryazhskaya, O.; Yakushev, V.; Anokhina, A.; Galkin, V.I.; Nikitina, V.; Osedlo, V.; Publichenko, P.; Roganova, T.; Aoki, S.; Hara, T.; Rokujo, H.; Ariga, A.; Ariga, T.; Ereditato, A.; Juget, F.; Knuesel, J.; Kreslo, I.; Lutter, G.; Meisel, F.; Moser, U.; Pistillo, C.; Pretzl, K.; Vuilleumier, J.L.; Autiero, D.; Brugiere, T.; Cazes, A.; Chaussard, L.; Declais, Y.; Marteau, J.; Pennacchio, E.; Tran, T.; Badertscher, A.; Lazzaro, C.; Rubbia, A.; Strauss, T.; Bagulya, A.; Chernyavsky, M.; Goncharova, L.; Orlova, G.; Polukhina, N.; Starkov, N.; Vladimirov, M.; Bertolin, A.; Dal Corso, F.; Dusini, S.; Besnier, M.; Duchesneau, D.; Favier, J.; Pessard, H.; Zghiche, A.; Bick, D.; Ebert, J.; Ferber, T.; Goellnitz, C.; Hagner, C.; Lenkeit, J.; Oldorf, C.; Schmidt Parzefall, W.; Wonsak, B.; Zimmermann, R.; Bozza, C.; D'Amato, G.; Grella, G.; Policastro, G.; Rescigno, R.; Romano, G.; Sirignano, C.; Brugnera, R.; Garfagnini, A.; Kose, U.; Brunetti, G.; Giacomelli, G.; Giorgini, M.; Mauri, N.; Pozzato, M.; Sioli, M.; Tenti, M.; Buontempo, S.; Chukanov, A.; Di Capua, F.; Marotta, A.; Migliozzi, P.; Scotto Lavina, L.; Tioukov, V.; Chiarella, V.; Felici, G.; Grianti, F.; Paniccia, M.; Paoloni, A.; Spinetti, M.; Terranova, F.; Votano, L.; Chon-Sen, N.; Dracos, M.; Jollet, C.; Meregaglia, A.; Cozzi, M.; D'Ambrosio, N.; Di Giovanni, A.; Esposito, L.S.; Gustavino, C.; De Lellis, G.; Russo, A.; Strolin, P.; De Serio, M.; Fini, R.; Ieva, M.; Di Ferdinando, D.; Mandrioli, G.; Medinaceli, E.; Patrizii, L.; Sirri, G.; Di Marco, N.; Monacelli, P.; Park, B.D.; Park, I.G.; Pupilli, F.; Dmitrievski, S.; Gornushkin, Y.; Naumov, D.; Olchevski, A.; Sheshukov, A.; Zemskova, S.; Egorov, O.; Golubkov, D.; Rostovtseva, I.; Zaitsev, Y.; Frekers, D.; Pilipenko, V.; Fukuda, T.; Hamada, K.; Hoshino, K.; Kazuyama, M.; Komatsu, M.; Kubota, H.; Miyamoto, S.; Morishima, K.; Naganawa, N.; Naka, T.; Nakamura, M.; Nakano, T.; Niwa, K.; Nonoyama, Y.; Sato, O.; Takahashi, S.; Yoshioka, T.; Yoshida, J.; Fukushima, C.; Kimura, M.; Matsuo, T.; Mikado, S.; Ogawa, S.; Shibuya, H.; Goldberg, J.; Guler, M.; Tolun, P.; Tufanli, S.; Hierholzer, M.; Jakovcic, K.; Klicek, B.; Ljubicic, A.; Stipcevic, M.; Kim, S.H.; Song, J.S.; Yoon, C.S.; Kodama, K.; Longhin, A.; Stanco, L.; Muciaccia, M.T.; Pastore, A.; Simone, S.; Rosa, G.; Schembri, A.; Sato, Y.; Tezuka, I.; Schroeder, H.; Vilain, P.; Wilquet, G.

2010-01-01

The OPERA detector at the Gran Sasso underground laboratory (LNGS) was used to measure the atmospheric muon charge ratio R μ =N μ + /N μ - in the TeV energy region. We analyzed 403069 atmospheric muons corresponding to 113.4 days of lifetime during the 2008 CNGS run. We computed separately the muon charge ratio for single and for multiple muon events in order to select different energy regions of the primary cosmic ray spectrum and to test the R μ dependence on the primary composition. The measured R μ values were corrected taking into account the charge-misidentification errors. Data have also been grouped in five bins of the ''vertical surface energy'' E μ cos θ. A fit to a simplified model of muon production in the atmosphere allowed the determination of the pion and kaon charge ratios weighted by the cosmic ray energy spectrum. (orig.)

Thomson scattering measurements in atmospheric plasma jets

International Nuclear Information System (INIS)

Gregori, G.; Schein, J.; Schwendinger, P.; Kortshagen, U.; Heberlein, J.; Pfender, E.

1999-01-01

Electron temperature and electron density in a dc plasma jet at atmospheric pressure have been obtained using Thomson laser scattering. Measurements performed at various scattering angles have revealed effects that are not accounted for by the standard scattering theory. Differences between the predicted and experimental results suggest that higher order corrections to the theory may be required, and that corrections to the form of the spectral density function may play an important role. copyright 1999 The American Physical Society

In situ secondary organic aerosol formation from ambient pine forest air using an oxidation flow reactor

Science.gov (United States)

Palm, Brett B.; Campuzano-Jost, Pedro; Ortega, Amber M.; Day, Douglas A.; Kaser, Lisa; Jud, Werner; Karl, Thomas; Hansel, Armin; Hunter, James F.; Cross, Eben S.; Kroll, Jesse H.; Peng, Zhe; Brune, William H.; Jimenez, Jose L.

2016-03-01

An oxidation flow reactor (OFR) is a vessel inside which the concentration of a chosen oxidant can be increased for the purpose of studying SOA formation and aging by that oxidant. During the BEACHON-RoMBAS (Bio-hydro-atmosphere interactions of Energy, Aerosols, Carbon, H2O, Organics & Nitrogen-Rocky Mountain Biogenic Aerosol Study) field campaign, ambient pine forest air was oxidized by OH radicals in an OFR to measure the amount of SOA that could be formed from the real mix of ambient SOA precursor gases, and how that amount changed with time as precursors changed. High OH concentrations and short residence times allowed for semicontinuous cycling through a large range of OH exposures ranging from hours to weeks of equivalent (eq.) atmospheric aging. A simple model is derived and used to account for the relative timescales of condensation of low-volatility organic compounds (LVOCs) onto particles; condensational loss to the walls; and further reaction to produce volatile, non-condensing fragmentation products. More SOA production was observed in the OFR at nighttime (average 3 µg m-3 when LVOC fate corrected) compared to daytime (average 0.9 µg m-3 when LVOC fate corrected), with maximum formation observed at 0.4-1.5 eq. days of photochemical aging. SOA formation followed a similar diurnal pattern to monoterpenes, sesquiterpenes, and toluene+p-cymene concentrations, including a substantial increase just after sunrise at 07:00 local time. Higher photochemical aging (> 10 eq. days) led to a decrease in new SOA formation and a loss of preexisting OA due to heterogeneous oxidation followed by fragmentation and volatilization. When comparing two different commonly used methods of OH production in OFRs (OFR185 and OFR254-70), similar amounts of SOA formation were observed. We recommend the OFR185 mode for future forest studies. Concurrent gas-phase measurements of air after OH oxidation illustrate the decay of primary VOCs, production of small oxidized organic

In situ secondary organic aerosol formation from ambient pine forest air using an oxidation flow reactor

Directory of Open Access Journals (Sweden)

B. B. Palm

2016-03-01

Full Text Available An oxidation flow reactor (OFR is a vessel inside which the concentration of a chosen oxidant can be increased for the purpose of studying SOA formation and aging by that oxidant. During the BEACHON-RoMBAS (Bio-hydro-atmosphere interactions of Energy, Aerosols, Carbon, H2O, Organics & Nitrogen–Rocky Mountain Biogenic Aerosol Study field campaign, ambient pine forest air was oxidized by OH radicals in an OFR to measure the amount of SOA that could be formed from the real mix of ambient SOA precursor gases, and how that amount changed with time as precursors changed. High OH concentrations and short residence times allowed for semicontinuous cycling through a large range of OH exposures ranging from hours to weeks of equivalent (eq. atmospheric aging. A simple model is derived and used to account for the relative timescales of condensation of low-volatility organic compounds (LVOCs onto particles; condensational loss to the walls; and further reaction to produce volatile, non-condensing fragmentation products. More SOA production was observed in the OFR at nighttime (average 3 µg m−3 when LVOC fate corrected compared to daytime (average 0.9 µg m−3 when LVOC fate corrected, with maximum formation observed at 0.4–1.5 eq. days of photochemical aging. SOA formation followed a similar diurnal pattern to monoterpenes, sesquiterpenes, and toluene+p-cymene concentrations, including a substantial increase just after sunrise at 07:00 local time. Higher photochemical aging (> 10 eq. days led to a decrease in new SOA formation and a loss of preexisting OA due to heterogeneous oxidation followed by fragmentation and volatilization. When comparing two different commonly used methods of OH production in OFRs (OFR185 and OFR254-70, similar amounts of SOA formation were observed. We recommend the OFR185 mode for future forest studies. Concurrent gas-phase measurements of air after OH oxidation illustrate the decay of primary VOCs, production

Large-sized SmBCO single crystals with T sub c over 93 K grown in atmospheric ambient by crystal pulling

CERN Document Server

Yao Xin; Shiohara, Y

2003-01-01

Sm sub 1 sub + sub x Ba sub 2 sub - sub x Cu sub 3 O sub z (SmBCO) single crystals were grown under atmospheric ambient by the top-seeded solution growth method. Inductively coupled plasma results indicate that there is negligible Sm substitution for Ba sites in the grown SmBCO crystals, although they crystallized from different Ba-Cu-O solvents with a wide composition range (Ba/Cu ratio of 0.5-0.6). As a result, these crystals show high superconducting critical transition temperature values (T sub c) of over 93 K with a sharp transition width after oxygenation. A large-sized crystal with an a-b plane of 23 x 22 mm sup 2 and a c-axis of 19 mm was obtained at a high growth rate of nearly 0.13 mm h sup - sup 1. In short, with more controllable thermodynamic parameters, SmBCO single crystals can readily achieve both large size and high superconducting properties. (rapid communication)

Desorption atmospheric pressure photoionization high-resolution mass spectrometry: a complementary approach for the chemical analysis of atmospheric aerosols

Czech Academy of Sciences Publication Activity Database

Parshintsev, J.; Vaikkinen, A.; Lipponen, K.; Vrkoslav, Vladimír; Cvačka, Josef; Kostiainen, R.; Kotiaho, T.; Hartonen, K.; Riekkola, M. L.; Kauppila, T. J.

2015-01-01

Roč. 29, č. 13 (2015), s. 1233-1241 ISSN 0951-4198 Grant - others:GA AV ČR(CZ) M200551204 Institutional support: RVO:61388963 Keywords : atmospheric aerosols * mass spectrometry * ambient ionization Subject RIV: CB - Analytical Chemistry , Separation Impact factor: 2.226, year: 2015

Experience with novel technologies for direct measurement of atmospheric NO2

Science.gov (United States)

Hueglin, Christoph; Hundt, Morten; Mueller, Michael; Schwarzenbach, Beat; Tuzson, Bela; Emmenegger, Lukas

2017-04-01

Nitrogen dioxide (NO2) is an air pollutant that has a large impact on human health and ecosystems, and it plays a key role in the formation of ozone and secondary particulate matter. Consequently, legal limit values for NO2 are set in the EU and elsewhere, and atmospheric observation networks typically include NO2 in their measurement programmes. Atmospheric NO2 is principally measured by chemiluminescence detection, an indirect measurement technique that requires conversion of NO2 into nitrogen monoxide (NO) and finally calculation of NO2 from the difference between total nitrogen oxides (NOx) and NO. Consequently, NO2 measurements with the chemiluminescence method have a relatively high measurement uncertainty and can be biased depending on the selectivity of the applied NO2 conversion method. In the past years, technologies for direct and selective measurement of NO2 have become available, e.g. cavity attenuated phase shift spectroscopy (CAPS), cavity enhanced laser absorption spectroscopy and quantum cascade laser absorption spectrometry (QCLAS). These technologies offer clear advantages over the indirect chemiluminescence method. We tested the above mentioned direct measurement techniques for NO2 over extended time periods at atmospheric measurement stations and report on our experience including comparisons with co-located chemiluminescence instruments equipped with molybdenum as well as photolytic NO2 converters. A still open issue related to the direct measurement of NO2 is instrument calibration. Accurate and traceable reference standards and NO2 calibration gases are needed. We present results from the application of different calibration strategies based on the use of static NO2 calibration gases as well as dynamic NO2 calibration gases produced by permeation and by gas-phase titration (GPT).

Electricity and environmental conservation; Electricidad y conservacion del medio ambiente

Energy Technology Data Exchange (ETDEWEB)

Rivas, Elena [ed.] [Instituto de Investigaciones Electricas, Temixco, Morelos (Mexico)

1999-07-01

This article presents a study on the environmental contamination of seven of the main fossil fuel power stations of the country. Experiment with water emulsions in fuel oil and with fluidized beds was carried out, which allow to burn fuels with efficiency, retaining the polluting compounds emitted to the atmosphere, which considers factors such as the wind turbulences, the atmospheric chemistry and the gas recirculation above the chimney, and the use of biogas to generate electricity which offers an ample potential of mitigation of the environmental contamination, characteristic of the garbage dumps. [Spanish] Este articulo presenta un estudio de contaminacion ambiental de siete de las principales centrales termoeletricas del pais. Se experimento con emulsiones de agua en combustoleo y los lechos fluidizados, los cuales permiten quemar combustibles con eficiencia reteniendo los compuestos contaminantes emitidos a la atmosfera, los cuales consideran factores como la turbulencia del viento, la quimica atmosferica y la recirculacion de gases sobre la chimenea, la utilizacion de biogas para generar electricidad el cual ofrece un amplio potencial de mitigacion de la contaminacion ambiental propia de los basureros.

Evaluation of factors affecting accurate measurements of atmospheric CO2 and CH4 by wavelength-scanned cavity ring-down spectroscopy

Science.gov (United States)

Nara, H.; Tanimoto, H.; Tohjima, Y.; Mukai, H.; Nojiri, Y.; Katsumata, K.; Rella, C.

2012-07-01

We examined potential interferences from water vapor and atmospheric background gases (N2, O2, and Ar), and biases by isotopologues of target species, on accurate measurement of atmospheric CO2 and CH4 by means of wavelength-scanned cavity ring-down spectroscopy (WS-CRDS). Variations in the composition of the background gas substantially impacted the CO2 and CH4 measurements: the measured amounts of CO2 and CH4 decreased with increasing N2 mole fraction, but increased with increasing O2 and Ar, suggesting that the pressure-broadening effects (PBEs) increased as Ar < O2 < N2. Using these experimental results, we inferred PBEs for the measurement of synthetic standard gases. The PBEs were negligible (up to 0.05 ppm for CO2 and 0.01 ppb for CH4) for gas standards balanced with purified air, although the PBEs were substantial (up to 0.87 ppm for CO2 and 1.4 ppb for CH4) for standards balanced with synthetic air. For isotopic biases on CO2 measurements, we compared experimental results and theoretical calculations, which showed excellent agreement within their uncertainty. We derived empirical correction functions for water vapor for three WS-CRDS instruments (Picarro EnviroSense 3000i, G-1301, and G-2301). Although the transferability of the functions was not clear, no significant difference was found in the water vapor correction values among these instruments within the typical analytical precision at sufficiently low water concentrations (< 0.3%V for CO2 and < 0.4%V for CH4). For accurate measurements of CO2 and CH4 in ambient air, we concluded that WS-CRDS measurements should be performed under complete dehumidification of air samples, or moderate dehumidification followed by application of a water vapor correction function, along with calibration by natural air-based standard gases or purified air-balanced synthetic standard gases with isotopic correction.

Radiological Programs- Ambient Radon at the Yucca Mountain Site (SCPB:NA)

International Nuclear Information System (INIS)

TRW

1999-01-01

This report summarizes the results of the ambient radon monitoring activities conducted by the Radiological/Environmental Field Programs Department of the Civilian Radioactive Waste Management and Operating Contractor (CRWMS M and O), Yucca Mountain Site Characterization Office. Overall, outdoor radon concentrations measured at the Yucca Mountain site were within the range of those reported for other areas in Nevada and the continental United States. Though there was some evidence of trends with time at some monitoring sites, regional atmospheric radon concentrations to date, do not appear to have changed significantly since the inception of site characterization activities. A preliminary dose assessment yielded an estimated annual effective dose equivalent of 134 mrem based on a continuous exposure to the average ambient radon concentration measured at the Yucca Mountain site. Concentrations were measured using two types of systems, passive electret ion chambers (EIC) and continuous radon monitors (CRM). The EICs produced time-averaged radon concentration data and the CRMs were used to study radon fluctuations over time. Between 1991 and 1995, the mean radon concentration at the site, as measured by EICs placed one meter above ground level, was 0.32 ± 0.15 pCi L -1 . Radon concentrations varied between monitoring locations and between years. Station NF38, located near the North Portal of the Exploratory Studies Facility (ESF), exhibited the highest overall average radon concentration at 0.55 pCi L -1 (1992 to 1995). Concentrations appear to cycle diurnally, generally peaking in the early morning hours and being lowest in the afternoon. The data also suggested that radon concentrations may fluctuate seasonally. The work accomplished between 1991 and 1995, established radon levels in the general area surrounding Yucca Mountain. It is recommended that further work focus directly on those locations that have the greatest potential for influencing ambient radon levels

Detection capability of the IMS seismic network based on ambient seismic noise measurements

Science.gov (United States)

Gaebler, Peter J.; Ceranna, Lars

2016-04-01

All nuclear explosions - on the Earth's surface, underground, underwater or in the atmosphere - are banned by the Comprehensive Nuclear-Test-Ban Treaty (CTBT). As part of this treaty, a verification regime was put into place to detect, locate and characterize nuclear explosion testings at any time, by anyone and everywhere on the Earth. The International Monitoring System (IMS) plays a key role in the verification regime of the CTBT. Out of the different monitoring techniques used in the IMS, the seismic waveform approach is the most effective technology for monitoring nuclear underground testing and to identify and characterize potential nuclear events. This study introduces a method of seismic threshold monitoring to assess an upper magnitude limit of a potential seismic event in a certain given geographical region. The method is based on ambient seismic background noise measurements at the individual IMS seismic stations as well as on global distance correction terms for body wave magnitudes, which are calculated using the seismic reflectivity method. From our investigations we conclude that a global detection threshold of around mb 4.0 can be achieved using only stations from the primary seismic network, a clear latitudinal dependence for the detection threshold can be observed between northern and southern hemisphere. Including the seismic stations being part of the auxiliary seismic IMS network results in a slight improvement of global detection capability. However, including wave arrivals from distances greater than 120 degrees, mainly PKP-wave arrivals, leads to a significant improvement in average global detection capability. In special this leads to an improvement of the detection threshold on the southern hemisphere. We further investigate the dependence of the detection capability on spatial (latitude and longitude) and temporal (time) parameters, as well as on parameters such as source type and percentage of operational IMS stations.

Influence of Ambient Gas on Laser-Induced Breakdown Spectroscopy of Uranium Metal

International Nuclear Information System (INIS)

Zhang Dacheng; Ma Xinwen; Wang Shulong; Zhu Xiaolong

2015-01-01

Laser-induced breakdown spectroscopy (LIBS) is regarded as a suitable method for the remote analysis of materials in any phase, even in an environment with high radiation levels. In the present work we used the third harmonic pulse of a Nd:YAG laser for ablation of uranium metal and measured the plasma emission with a fiber-optic spectrometer. The LIBS spectra of uranium metal and their features in different ambient gases (i.e., argon, neon, oxygen, and nitrogen) at atmospheric pressure were studied. Strong continuum spectrum and several hundreds of emission lines from UI and UII were observed. It is found that the continuum spectrum observed in uranium not only comes from bremsstrahlung emission but is also due to the complex spectrum of uranium. The influence of ambient gas and the gas flow rate for ablation of uranium metal was investigated. The experimental results indicate that the intensity of the uranium lines was enhanced in argon and nitrogen. However, the intensity of uranium lines was decreased in oxygen due to the generation of UO and other oxides. The results also showed that the highest intensity of uranium lines were obtained in argon gas with a gas flow rate above 2.5 L/min. The enhanced mechanism in ambient gas and the influence of the gas flow rate were analyzed in this work. (paper)

The Effect of Atmospheric Scattering as Inferred from the Rocket-Borne UV Radiometer Measurements

Directory of Open Access Journals (Sweden)

Jhoon Kim

1997-06-01

Full Text Available Radiometers in UV and visible wavelengths were onboard the Korean Sounding Rocket(KSR-1 and 2 which were launched on June 4th and September 1st, 1993. These radiometers were designed to capture the solar radiation during the ascending period of the rocket flight. The purpose of the instrument was to measure the vertical profiles of stratospheric ozone densities. Since the instrument measured the solar radiation from the ground to its apogee, it is possible to investigate the altitude variation of the measured intensity and to estimate the effect of atmospheric scattering by comparing the UV and visible intensity. The visible channel was a reference because the 450-nm wavelength is in the atmospheric window region, where the solar radiation is transmitted through the atmosphere without being absorbed by other atmospheric gases. The use of 450-nm channel intensity as a reference should be limited to the altitude ranges above the certain altitudes, say 20 to 25§° where the signals are not perturbed by atmospheric scattering effects.

Ultraviolet spectrophotometer for measuring columnar atmospheric ozone from aircraft

Science.gov (United States)

Hanser, F. A.; Sellers, B.; Briehl, D. C.

1978-01-01

An ultraviolet spectrophotometer (UVS) to measure downward solar fluxes from an aircraft or other high altitude platform is described. The UVS uses an ultraviolet diffuser to obtain large angular response with no aiming requirement, a twelve-position filter wheel with narrow (2-nm) and broad (20-nm) bandpass filters, and an ultraviolet photodiode. The columnar atmospheric ozone above the UVS (aircraft) is calculated from the ratios of the measured ultraviolet fluxes. Comparison with some Dobson station measurements gives agreement to 2%. Some UVS measured ozone profiles over the Pacific Ocean for November 1976 are shown to illustrate the instrument's performance.

Ambient diagnostics

CERN Document Server

Cai, Yang

2014-01-01

Part I. FundamentalsIntroductionWhat is Ambient Diagnostics?Diagnostic ModelsMultimedia IntelligenceCrowd SourcingSoft SensorsScience of SimplicityPersonal DiagnosesBasic AlgorithmsBasic ToolsSummaryProblemsTransformationEarly Discoveries of Heartbeat PatternsTransforms, Features, and AttributesSequential FeaturesSpatiotemporal FeaturesShape FeaturesImagery FeaturesFrequency Domain FeaturesMulti-Resolution FeaturesSummaryProblemsPattern RecognitionSimilarities and DistancesClustering MethodsClassification MethodsClassifier Accuracy MeasuresSummaryProblemsPart II. Multimedia IntelligenceSound RecognitionMicrophone AppsModern Acoustic Transducers (Microphones)Frequency Response CharacteristicsDigital Audio File FormatsHeart Sound SensingLung Sound SensingSnore MeterSpectrogram (STFT)Ambient Sound AnalysisSound RecognitionRecognizing Asthma SoundPeak ShiftFeature CompressionRegroupingNoise IssuesFuture ApplicationsSummaryProblemsColor SensorsColor SensingHuman Color VisionColor SensorsColor Matching ExperimentsC...

Impact of coal combustion from thermal power plant: estimates on ambient SO2 levels

International Nuclear Information System (INIS)

Joshi, P.V.

1991-01-01

Using a Gaussian dispersion model, ambient Ground Levels Concentrations (GLC) of SO 2 due to Nashik Thermal Power Plant have been computed. Annual GLC in 16 cardinal sectors and concentration levels in 6 atmospheric stability classes have been estimated as a function of down wind distance. The values are compared with national ambient air quality standard and risk involved due to the release of SO 2 from power plant has been assessed. (author). 8 refs., 2 appendixes

Comparison of OH reactivity measurements in the atmospheric simulation chamber SAPHIR

Science.gov (United States)

Fuchs, Hendrik; Novelli, Anna; Rolletter, Michael; Hofzumahaus, Andreas; Pfannerstill, Eva Y.; Kessel, Stephan; Edtbauer, Achim; Williams, Jonathan; Michoud, Vincent; Dusanter, Sebastien; Locoge, Nadine; Zannoni, Nora; Gros, Valerie; Truong, Francois; Sarda-Esteve, Roland; Cryer, Danny R.; Brumby, Charlotte A.; Whalley, Lisa K.; Stone, Daniel; Seakins, Paul W.; Heard, Dwayne E.; Schoemaecker, Coralie; Blocquet, Marion; Coudert, Sebastien; Batut, Sebastien; Fittschen, Christa; Thames, Alexander B.; Brune, William H.; Ernest, Cheryl; Harder, Hartwig; Muller, Jennifer B. A.; Elste, Thomas; Kubistin, Dagmar; Andres, Stefanie; Bohn, Birger; Hohaus, Thorsten; Holland, Frank; Li, Xin; Rohrer, Franz; Kiendler-Scharr, Astrid; Tillmann, Ralf; Wegener, Robert; Yu, Zhujun; Zou, Qi; Wahner, Andreas

2017-10-01

Hydroxyl (OH) radical reactivity (kOH) has been measured for 18 years with different measurement techniques. In order to compare the performances of instruments deployed in the field, two campaigns were conducted performing experiments in the atmospheric simulation chamber SAPHIR at Forschungszentrum Jülich in October 2015 and April 2016. Chemical conditions were chosen either to be representative of the atmosphere or to test potential limitations of instruments. All types of instruments that are currently used for atmospheric measurements were used in one of the two campaigns. The results of these campaigns demonstrate that OH reactivity can be accurately measured for a wide range of atmospherically relevant chemical conditions (e.g. water vapour, nitrogen oxides, various organic compounds) by all instruments. The precision of the measurements (limit of detection CRM) has a higher limit of detection of 2 s-1 at a time resolution of 10 to 15 min. The performances of the instruments were systematically tested by stepwise increasing, for example, the concentrations of carbon monoxide (CO), water vapour or nitric oxide (NO). In further experiments, mixtures of organic reactants were injected into the chamber to simulate urban and forested environments. Overall, the results show that the instruments are capable of measuring OH reactivity in the presence of CO, alkanes, alkenes and aromatic compounds. The transmission efficiency in Teflon inlet lines could have introduced systematic errors in measurements for low-volatile organic compounds in some instruments. CRM instruments exhibited a larger scatter in the data compared to the other instruments. The largest differences to reference measurements or to calculated reactivity were observed by CRM instruments in the presence of terpenes and oxygenated organic compounds (mixing ratio of OH reactants were up to 10 ppbv). In some of these experiments, only a small fraction of the reactivity is detected. The accuracy of CRM

Formation of nitro-PAHs from the heterogeneous reaction of ambient particle-bound PAHs with NO3/N2O5

Science.gov (United States)

Zimmermann, K.; Jariyasopit, N.; Simonich, S. L.; Atkinson, R.; Arey, J.

2012-12-01

Polycyclic aromatic hydrocarbons (PAHs) and their nitrated derivatives (nitro-PAHs) have been shown to be mutagenic in bacterial and mammalian assays and are classified as probable human carcinogens. Semi-volatile PAHs partition between the gas and particulate phases, depending on their liquid-phase vapor pressures and ambient temperatures. These PAHs have been extensively measured in ambient particulate matter and can ultimately undergo long-range transport from source regions (e.g., China to the western USA) (1). During transport these particle-bound PAHs may undergo reaction with NO3/N2O5 to form nitro-PAH derivatives. Previous studies of heterogeneous nitration of PAHs have used particles composed of graphite, diesel soot, and wood smoke (2-4). This study investigates the heterogeneous formation of nitro-PAHs from ambient particle-bound PAHs from Beijing, China and sites located within the Los Angeles air basin. These ambient particle samples, along with filters coated with isotopically labeled PAHs, were exposed to a mix of NO2/NO3/N2O5 in a 7000 L Teflon chamber, with analysis focused on the heterogeneous formation of molecular weight 247 and 273 nitro-PAHs. The heterogeneous formation of certain nitro-PAHs (including1-nitropyrene and 1- and 2-nitrotriphenylene) was observed for some, but not all, ambient samples. Formation of nitro-PAHs typically formed through gas-phase reactions (2-nitrofluoranthene and 2-nitropyrene) was not observed. The effect of particle age and local photochemical conditions during sampling on the degree of nitration in environmental chamber reactions, as well as ambient implications, will be presented. 1. Primbs, T.; Simonich, S.; Schmedding, D.; Wilson, G.; Jaffe, D.; Takami, A.; Kato, S.; Hatakeyama, S.; Kajii, Y. Environ. Sci. Technol. 2007, 41, 3551-3558. 2. Esteve, W.; Budzinski, H.; Villenave, E. Atmospheric Environment 2004, 38, 6063-6072. 3. Nguyen, M.; Bedjanian, Y.; Guilloteau, A. Journal of Atmospheric Chemistry 2009, 62

Atmospheric implications of simultaneous nighttime measurements of NO3 radicals and hono

International Nuclear Information System (INIS)

Pitts, J.N. Jr.; Biermann, H.W.; Atkinson, R.; Winer, A.M.

1984-01-01

Atmospheric concentrations of gaseous HONO and the NO 3 radical were measured simultaneously for the first time using long path differential optical absorption spectroscopy. Diurnal profiles are reported for two successive nights following days of moderate pollution at Riverside, California, together with concurrent measurements of NO 2 , O 3 and NO concentrations and an upper limit for HCHO levels. These measurements permit an examination of selected aspects of the nighttime atmospheric chemistry of HONO and the NO 3 radical and related species. Our data do not support a recently proposed homogeneous gas phase mechanism for HONO formation initiated by the reaction of the NO 3 radical with HCHO

Mid-infrared photoacoustic spectroscopy for atmospheric NO2 measurements

Science.gov (United States)

Lassen, Mikael; Lamard, Laurent; Balslev-Harder, David; Peremans, Andre; Petersen, Jan C.

2018-02-01

A photoacoustic (PA) sensor for spectroscopic measurements of NO2-N2 at ambient pressure and temperature is demonstrated. The PA sensor is pumped resonantly by a nanosecond pulsed single-mode mid-infrared (MIR) optical parametric oscillator (OPO). Spectroscopic measurements of NO2-N2 in the 3.25 μm to 3.55 μm wavelength region with a resolution bandwidth of 5 cm-1 and with a single shot detection limit of 1.6 ppmV (μmol/mol) is demonstrated. The measurements were conducted with a constant flow rate of 300 ml/min, thus demonstrating the suitability of the gas sensor for real time trace gas measurements. The acquired spectra is compared with data from the Hitran database and good agreement is found. An Allan deviation analysis shows that the detection limit at optimum integration time for the PAS sensor is 14 ppbV (nmol/mol) at 170 seconds of integration time, corresponding to a normalized noise equivalent absorption (NNEA) coefficient of 3.3×10-7 W cm-1 Hz-1/2.

Atmospheric Radiation Measurement Climate Research Facility (ACRF) Annual Report 2008

Energy Technology Data Exchange (ETDEWEB)

LR Roeder

2008-12-01

The Importance of Clouds and Radiation for Climate Change: The Earth’s surface temperature is determined by the balance between incoming solar radiation and thermal (or infrared) radiation emitted by the Earth back to space. Changes in atmospheric composition, including greenhouse gases, clouds, and aerosols, can alter this balance and produce significant climate change. Global climate models (GCMs) are the primary tool for quantifying future climate change; however, there remain significant uncertainties in the GCM treatment of clouds, aerosol, and their effects on the Earth’s energy balance. In 1989, the U.S. Department of Energy (DOE) Office of Science created the Atmospheric Radiation Measurement (ARM) Program to address scientific uncertainties related to global climate change, with a specific focus on the crucial role of clouds and their influence on the transfer of radiation in the atmosphere. To reduce these scientific uncertainties, the ARM Program uses a unique twopronged approach: • The ARM Climate Research Facility, a scientific user facility for obtaining long-term measurements of radiative fluxes, cloud and aerosol properties, and related atmospheric characteristics in diverse climate regimes; and • The ARM Science Program, focused on the analysis of ACRF and other data to address climate science issues associated with clouds, aerosols, and radiation, and to improve GCMs. This report provides an overview of each of these components and a sample of achievements for each in fiscal year (FY) 2008.

Investigation of hydrophobic substrates for solution residue analysis utilizing an ambient desorption liquid sampling-atmospheric pressure glow discharge microplasma.

Science.gov (United States)

Paing, Htoo W; Marcus, R Kenneth

2018-03-12

A practical method for preparation of solution residue samples for analysis utilizing the ambient desorption liquid sampling-atmospheric pressure glow discharge optical emission spectroscopy (AD-LS-APGD-OES) microplasma is described. Initial efforts involving placement of solution aliquots in wells drilled into copper substrates, proved unsuccessful. A design-of-experiment (DOE) approach was carried out to determine influential factors during sample deposition including solution volume, solute concentration, number of droplets deposited, and the solution matrix. These various aspects are manifested in the mass of analyte deposited as well as the size/shape of the product residue. Statistical analysis demonstrated that only those initial attributes were significant factors towards the emission response of the analyte. Various approaches were investigated to better control the location/uniformity of the deposited sample. Three alternative substrates, a glass slide, a poly(tetrafluoro)ethylene (PTFE) sheet, and a polydimethylsiloxane (PDMS)-coated glass slide, were evaluated towards the microplasma analytical performance. Co-deposition with simple organic dyes provided an accurate means of determining the location of the analyte with only minor influence on emission responses. The PDMS-coated glass provided the best performance by virtue of its providing a uniform spatial distribution of the residue material. This uniformity yielded an improved limits of detection by approximately 22× for 20 μL and 4 x for 2 μL over the other two substrates. While they operate by fundamentally different processes, this choice of substrate is not restricted to the LS-APGD, but may also be applicable to other AD methods such as DESI, DART, or LIBS. Further developments will be directed towards a field-deployable ambient desorption OES source for quantitative analysis of microvolume solution residues of nuclear forensics importance.

Measuring the spectral emissivity of thermal protection materials during atmospheric reentry simulation

Science.gov (United States)

Marble, Elizabeth

1996-01-01

Hypersonic spacecraft reentering the earth's atmosphere encounter extreme heat due to atmospheric friction. Thermal Protection System (TPS) materials shield the craft from this searing heat, which can reach temperatures of 2900 F. Various thermophysical and optical properties of TPS materials are tested at the Johnson Space Center Atmospheric Reentry Materials and Structures Evaluation Facility, which has the capability to simulate critical environmental conditions associated with entry into the earth's atmosphere. Emissivity is an optical property that determines how well a material will reradiate incident heat back into the atmosphere upon reentry, thus protecting the spacecraft from the intense frictional heat. This report describes a method of measuring TPS emissivities using the SR5000 Scanning Spectroradiometer, and includes system characteristics, sample data, and operational procedures developed for arc-jet applications.

Hazard surveillance for workplace magnetic fields. 1: Walkaround sampling method for measuring ambient field magnitude; 2: Field characteristics from waveform measurements

Energy Technology Data Exchange (ETDEWEB)

Methner, M.M.; Bowman, J.D.

1998-03-01

Recent epidemiologic research has suggested that exposure to extremely low frequency (ELF) magnetic fields (MF) may be associated with leukemia, brain cancer, spontaneous abortions, and Alzheimer`s disease. A walkaround sampling method for measuring ambient ELF-MF levels was developed for use in conducting occupational hazard surveillance. This survey was designed to determine the range of MF levels at different industrial facilities so they could be categorized by MF levels and identified for possible subsequent personal exposure assessments. Industries were selected based on their annual electric power consumption in accordance with the hypothesis that large power consumers would have higher ambient MFs when compared with lower power consumers. Sixty-two facilities within thirteen 2-digit Standard Industrial Classifications (SIC) were selected based on their willingness to participate. A traditional industrial hygiene walkaround survey was conducted to identify MF sources, with a special emphasis on work stations.

Novel Semi-Direct OH Reactivity (kOH) Measurements by Chemical Ionization Mass Spectrometry during a Chamber Instrument Comparison Campaign and Continuous Ambient Air Sampling at a Central European GAW Station

Science.gov (United States)

Muller, J.; Kubistin, D.; Elste, T.; Plass-Duelmer, C.; Claude, A.; Englert, J.; Holla, R.; Fuchs, H.; Hofzumahaus, A.; Holland, F.; Novelli, A.; Tillmann, R.; Wegener, R.; Rohrer, F.; Yu, Z.; Bohn, B.; Williams, J.; Pfannerstill, E.; Edtbauer, A.; Kluepfel, T.

2016-12-01

Total OH reactivity (kOH) has been recognized as a useful measure to gauge the potential atmospheric oxidation capacity and a few different in-situ measurement techniques have been developed over the last 15 years. Here results are presented from a novel semi-direct method developed by the German Weather Service (DWD) utilizing a chemical ionization mass spectrometer (CIMS). Recently in April 2016, the CIMS system participated in a half-blind kOH instrument comparison campaign at the Forschungszentrum Jülich (FZJ) SAPHIR chamber. Experiments provided controlled conditions with a range of different VOC mixtures and varying NOx levels, representing environments dominated by biogenic or urban emissions. Alongside CIMS, kOH was also measured by systems using the comparative reactivity method (CRM) and the pump-probe technique with OH detection. The intercomparison revealed a good performance of CIMS at lower OH reactivities (0-15 s-1), a range for which the instrumental set up was optimized. Limitations of the CIMS system consist of an upper limit for kOH detection and the need for applying a chemical correction function as a result of instrument-internal HOx recycling. Findings and instrument parameters obtained from the FZJ SAPHIR campaign and flow tube experiments are then applied to ambient air kOH measurements at the Meteorological Observatory Hohenpeissenberg (MOHp), Germany. The CIMS instrument is used there for long-term measurements of OH, H2SO4, ROx and kOH. Here, we show ambient air kOH measurements, interpreted in conjunction with volatile organic compounds (VOC) and inorganic trace gases also measured at the GAW station Hohenpeissenberg. These observations provide a unique dataset to investigate turnover rates and seasonal cycles of reactive trace gases, i.e. sources that make up total OH reactivity in this central European, rural setting.

Methyl chavicol: characterization of its biogenic emission rate, abundance, and oxidation products in the atmosphere

Directory of Open Access Journals (Sweden)

N. C. Bouvier-Brown

2009-03-01

Full Text Available We report measurements of ambient atmospheric mixing ratios for methyl chavicol and determine its biogenic emission rate. Methyl chavicol, a biogenic oxygenated aromatic compound, is abundant within and above Blodgett Forest, a ponderosa pine forest in the Sierra Nevada Mountains of California. Methyl chavicol was detected simultaneously by three in-situ instruments – a gas chromatograph with mass spectrometer detector (GC-MS, a proton transfer reaction mass spectrometer (PTR-MS, and a thermal desorption aerosol GC-MS (TAG – and found to be abundant within and above Blodgett Forest. Methyl chavicol atmospheric mixing ratios are strongly correlated with 2-methyl-3-buten-2-ol (MBO, a light- and temperature-dependent biogenic emission from the ponderosa pine trees at Blodgett Forest. Scaling from this correlation, methyl chavicol emissions account for 4–68% of the carbon mass emitted as MBO in the daytime, depending on the season. From this relationship, we estimate a daytime basal emission rate of 0.72–10.2 μgCg⁻¹ h⁻¹, depending on needle age and seasonality. We also present the first observations of its oxidation products (4-methoxybenzaldehyde and 4-methyoxy benzene acetaldehyde in the ambient atmosphere. Methyl chavicol is a major essential oil component of many plant species. This work suggests that methyl chavicol plays a significant role in the atmospheric chemistry of Blodgett Forest, and potentially other sites, and should be included explicitly in both biogenic volatile organic carbon emission and atmospheric chemistry models.

Spectral light absorption by ambient aerosols influenced by biomass burning in the Amazon Basin. I: Comparison and field calibration of absorption measurement techniques

Directory of Open Access Journals (Sweden)

O. Schmid

2006-01-01

Full Text Available Spectral aerosol light absorption is an important parameter for the assessment of the radiation budget of the atmosphere. Although on-line measurement techniques for aerosol light absorption, such as the Aethalometer and the Particle Soot Absorption Photometer (PSAP, have been available for two decades, they are limited in accuracy and spectral resolution because of the need to deposit the aerosol on a filter substrate before measurement. Recently, a 7-wavelength (λ Aethalometer became commercially available, which covers the visible (VIS to near-infrared (NIR spectral range (λ=450–950 nm, and laboratory calibration studies improved the degree of confidence in these measurement techniques. However, the applicability of the laboratory calibration factors to ambient conditions has not been investigated thoroughly yet. As part of the LBA-SMOCC (Large scale Biosphere atmosphere experiment in Amazonia – SMOke aerosols, Clouds, rainfall and Climate campaign from September to November 2002 in the Amazon basin we performed an extensive field calibration of a 1-λ PSAP and a 7-λ Aethalometer utilizing a photoacoustic spectrometer (PAS, 532 nm as reference device. Especially during the dry period of the campaign, the aerosol population was dominated by pyrogenic emissions. The most pronounced artifact of integrating-plate type attenuation techniques (e.g. Aethalometer, PSAP is due to multiple scattering effects within the filter matrix. For the PSAP, we essentially confirmed the laboratory calibration factor by Bond et al. (1999. On the other hand, for the Aethalometer we found a multiple scattering enhancement of 5.23 (or 4.55, if corrected for aerosol scattering, which is significantly larger than the factors previously reported (~2 for laboratory calibrations. While the exact reason for this discrepancy is unknown, the available data from the present and previous studies suggest aerosol mixing (internal versus external as a likely cause. For

Measuring Mass-Based Hygroscopicity of Atmospheric Particles through in situ Imaging

Energy Technology Data Exchange (ETDEWEB)

Piens, Dominique` Y.; Kelly, Stephen T.; Harder, Tristan; Petters, Markus D.; O' Brien, Rachel; Wang, Bingbing; Teske, Ken; Dowell, Pat; Laskin, Alexander; Gilles, Mary K.

2016-04-18

Quantifying how atmospheric particles interact with water vapor is critical for understanding the effects of aerosols on climate. We present a novel method to measure the mass-based hygroscopicity of particles while characterizing their elemental and carbon functional group compositions. Since mass-based hygroscopicity is insensitive to particle geometry, it is advantageous for probing the hygroscopic behavior of atmospheric particles, which can have irregular morphologies. Combining scanning electron microscopy with energy dispersive X-ray analysis (SEM/EDX), scanning transmission X-ray microscopy (STXM) analysis, and in situ STXM humidification experiments, this method was validated using laboratory-generated, atmospherically relevant particles. Then, the hygroscopicity and elemental composition of 15 complex atmospheric particles were analyzed by leveraging quantification of C, N, and O from STXM, and complementary elemental quantification from SEM/EDX. We found three types of hygroscopic responses, and correlated high hygroscopicity with Na and Cl content. The mixing state determined for 158 particles broadly agreed with those of the humidified particles, indicating the potential to infer the atmospheric hygroscopic behavior from a selected subset of particles. These methods offer unique quantitative capabilities to characterize and correlate the hygroscopicity and chemistry of individual submicron atmospheric particles.

Inter-hemispheric gradient of atmospheric trace gases in the Pacific

International Nuclear Information System (INIS)

Lowe, D.; Manning, M.; Brailsford, G.; Bromley, T.; Moss, R.; Ferretti, D.

1997-01-01

Measurements of atmospheric trace gases show that the concentrations and isotopic compositions of these species can change dramatically across the intertropical convergence zone (ITCZ) separating the two hemispheres. Because the anthropogenic sources of virtually all trace gases are greater in the northern than in the southern hemisphere, concentrations of the species are lower in the southern hemisphere. Typically the concentration gradient is inversely proportional to the lifetime of the trace gas in the atmosphere. Hence understanding the transport across the ITCZ is crucial to determining the variation of important trace gases in the New Zealand region. Container ships are being used to collect large clean air samples on voyages across the Pacific on great circle routes between Auckland (New Zealand), Honolulu (Hawaii) and Los Angeles and Seattle on the US West coast. Measurements on these samples are being used to supplement extensive carbon isotope measurements of atmospheric methane made at fixed sites in the southern hemisphere: Baring Head (New Zealand), Suva (Fiji) and Scott Base (Antarctica) to provide information on the global methane cycle. The authors present the first results of high precision measurements of the stable isotopes of atmospheric carbon monoxide and methane in transects across the equator. These have been obtained using a Finnigan MAT 252 high precision isotope ratio mass spectrometer with a modified miniature inlet system and a stringent calibration protocol. Overall precision for δ 13 C in ambient methane and carbon monoxide in clean air approaches 0.02 per thousand which helps provide information on several subtle processes controlling the abundance of the trace gases in the atmosphere. The 13 C in methane and carbon dioxide data show remarkable seasonal variations across the intertropical convergence zone (ITCZ) and may be used to infer aspects of transport of gases to extra tropical regions in the southern hemisphere

Sustained diffusive alternating current gliding arc discharge in atmospheric pressure air

DEFF Research Database (Denmark)

Zhu, Jiajian; Gao, Jinlong; Li, Zhongshan

2014-01-01

Rapid transition from glow discharge to thermal arc has been a common problem in generating stable high-power non-thermal plasmas especially at ambient conditions. A sustained diffusive gliding arc discharge was generated in a large volume in atmospheric pressure air, driven by an alternating...... current (AC) power source. The plasma column extended beyond the water-cooled stainless steel electrodes and was stabilized by matching the flow speed of the turbulent air jet with the rated output power. Comprehensive investigations were performed using high-speed movies measured over the plasma column...

Atmospheric Methane characterisation over the South African interior

CSIR Research Space (South Africa)

Feig, Gregor T

2016-10-01

Full Text Available The concentrations of atmospheric methane have an important impact on the global climate system and are important in the production of tropospheric ozone as it acts as an ozone precursor. The ambient concentrations of methane have increased more...

Atmospheric Radiation Measurement (ARM) Climate Research Facility Management Plan

Energy Technology Data Exchange (ETDEWEB)

Mather, James [Pacific Northwest National Lab. (PNNL), Richland, WA (United States)

2016-04-01

Mission and Vision Statements for the U.S. Department of Energy (DOE)’s Atmospheric Radiation Measurement (ARM) Climate Research Facility Mission The ARM Climate Research Facility, a DOE scientific user facility, provides the climate research community with strategically located in situ and remote-sensing observatories designed to improve the understanding and representation, in climate and earth system models, of clouds and aerosols as well as their interactions and coupling with the Earth’s surface. Vision To provide a detailed and accurate description of the Earth atmosphere in diverse climate regimes to resolve the uncertainties in climate and Earth system models toward the development of sustainable solutions for the nation's energy and environmental challenges.

Development of Rayleigh Doppler lidar for measuring middle atmosphere winds

Science.gov (United States)

Raghunath, K.; Patra, A. K.; Narayana Rao, D.

Interpretation of most of the middle and upper atmospheric dynamical and chemical data relies on the climatological description of the wind field Rayleigh Doppler lidar is one instrument which monitors wind profiles continuously though continuity is limited to clear meteorological conditions in the middle atmosphere A Doppler wind lidar operating in incoherent mode gives excellent wind and temperature information at these altitudes with necessary spectral sensitivity It observes atmospheric winds by measuring the spectral shift of the scattered light due to the motions of atmospheric molecules with background winds and temperature by spectral broadening The presentation is about the design and development of Incoherent Doppler lidar to obtain wind information in the height regions of 30-65 km The paper analyses and describes various types of techniques that can be adopted viz Edge technique and Fringe Imaging technique The paper brings out the scientific objectives configuration simulations error sources and technical challenges involved in the development of Rayleigh Doppler lidar The presentation also gives a novel technique for calibrating the lidar

Satellite data sets for the atmospheric radiation measurement (ARM) program

Energy Technology Data Exchange (ETDEWEB)

Shi, L.; Bernstein, R.L. [SeaSpace Corp., San Diego, CA (United States)

1996-04-01

This abstract describes the type of data obtained from satellite measurements in the Atmospheric Radiation Measurement (ARM) program. The data sets have been widely used by the ARM team to derive cloud-top altitude, cloud cover, snow and ice cover, surface temperature, water vapor, and wind, vertical profiles of temperature, and continuoous observations of weather needed to track and predict severe weather.

Re-tuning tuned mass dampers using ambient vibration measurements

International Nuclear Information System (INIS)

Hazra, B; Sadhu, A; Narasimhan, S; Lourenco, R

2010-01-01

Deterioration, accidental changes in the operating conditions, or incorrect estimates of the structure modal properties lead to de-tuning in tuned mass dampers (TMDs). To restore optimal performance, it is necessary to estimate the modal properties of the system, and re-tune the TMD to its optimal state. The presence of closely spaced modes and a relatively large amount of damping in the dominant modes renders the process of identification difficult. Furthermore, the process of estimating the modal properties of the bare structure using ambient vibration measurements of the structure with the TMD is challenging. In order to overcome these challenges, a novel identification and re-tuning algorithm is proposed. The process of identification consists of empirical mode decomposition to separate the closely spaced modes, followed by the blind identification of the remaining modes. Algorithms for estimating the fundamental frequency and the mode shape of the primary structure necessary for re-tuning the TMD are proposed. Experimental results from the application of the proposed algorithms to identify and re-tune a laboratory structure TMD system are presented

Measurement of radioactive aerosols as an original indicator of atmospheric pollution in urban areas

International Nuclear Information System (INIS)

Le Petit, G.; Millies-Lacroix, J. C.

1998-01-01

The Service Radioanalyses, Chimie et Environnment (Departement Analyses Surveillance de l'Environnement) of the French Atomic Energy Commission, located in suburban Paris, has for many years been conducting atmospheric radioactivity measurements. Since 1994, the laboratory has been using high volume air samplers equipped with filters for the weekly collection of atmospheric aerosols at a mean rate of about 600 m 3 .h -1 . The polypropylene filters, with a collection efficiency in excess of 93%, are compacted after sampling. The atmospheric radioactivity is measured by HP Ge gamma spectrometry after decay of short-lived natural relationship products. A study conducted in 1996 shows good correlation between the evolution with time of some of the indicators routinely used by AIRPARIF, the organization in charge of monitoring the air quality in the Ile-de-France region, to measure atmospheric pollution in the Paris area (SO 2 , NO) and that related to radioactivity of terrestrial ( 210 Pb, 40 K) and anthropogenic ( 137 Cs) origin, as well as the amount of aerosols collected. Further, the distribution in time of the atmospheric radioactivity of cosmogenic origin ( 7 Be) shows a yearly evolution somewhat similar to that observed with ozone

Formation of hydrophobic coating on glass surface using atmospheric pressure non-thermal plasma in ambient air

International Nuclear Information System (INIS)

Fang, Z; Qiu, Y; Kuffel, E

2004-01-01

Non-thermal plasmas under atmospheric pressure are of great interest in material surface processing because of their convenience, effectiveness and low cost. In this paper, the treatment of a glass surface for improving hydrophobicity using a non-thermal plasma generated by a dielectric barrier corona discharge (DBCD) with a needle array-to-plane electrode arrangement in atmospheric air is conducted, and the surface properties of the glass before and after the DBCD treatment are studied using contact angle measurement, surface resistance measurement and the wet flashover voltage test. The effects of the plasma dose (the product of average discharge power and treatment time) of DBCD on the surface modification are studied, and the mechanism of interaction between the plasma and glass surface is discussed. It is found that a layer of hydrophobic coating is formed on the glass surface through DBCD treatment, and the improvement of hydrophobicity depends on the plasma dose of the DBCD. It seems that there is an optimum plasma dose for the surface treatment. The test results of thermal ageing and chemical ageing show that the hydrophobic layer has quite stable characteristics

Ambient pressure sensitivity of microbubbles investigated through a parameter study

DEFF Research Database (Denmark)

Andersen, Klaus Scheldrup; Jensen, Jørgen Arendt

2009-01-01

Measurements on microbubbles clearly indicate a relation between the ambient pressure and the acoustic behavior of the bubble. The purpose of this study was to optimize the sensitivity of ambient pressure measurements, using the subharmonic component, through microbubble response simulations....... The behavior of two microbubbles corresponding to two different contrast agents was investigated as a function of driving pulse and ambient overpressure, pov. Simulations of Levovist using a rectangular driving pulse show an almost linear reduction in the subharmonic component as pov is increased. For a 20...... found, although the reduction is not completely linear as a function of the ambient pressure....

Long-term sub second-response monitoring of gaseous ammonia in ambient air by positive inhaling ion mobility spectrometry.

Science.gov (United States)

Huang, Wei; Wang, Weiguo; Chen, Chuang; Li, Mei; Peng, Liying; Li, Hang; Liu, Jiwei; Hou, Keyong; Li, Haiyang

2017-12-01

A real-time dynamic measurements of ammonia (NH 3 ) is crucial for understanding the atmospheric nucleation process. A novel method was developed for on line monitoring at the sub-second time scale for the gaseous ammonia in ambient air for months, based on a positive inhaling ion mobility spectrometry (IMS) with a 63 Ni ion source. The selective detection of NH 3 was achieved using a high resolution IMS with an optimization of the drift tube temperature above 150°C. This method improved the peak-to-peak resolution significantly, thus avoided the interferences of the adjacent peaks to the quantitative analysis of NH 3 . The time resolution of the IMS was less than 0.1s at a data averaging of 10 times. The limit of detection (LOD) achieved at sub-ppb level while a linear response of peak intensity versus concentration of NH 3 in the range of 10-60ppb and 60-400ppb were obtained. The relative standard deviations (RSD), the confidence level and the errors were 1.06%, 95% and ± 0.21ppb by measuring 100ppb NH 3 for 100 times. The effect of ambient humidity could be greatly reduced by using the drift temperature of over 150°C. At last, the application of measuring the NH 3 concentration evolutions of Dalian city was performed from June 19 to December 3 in 2015. The results illustrated a potential method of using IMS for a real-time measuring atmospheric NH 3 at an unprecedented accuracy and sensitivity with long-term stability. Copyright © 2017 Elsevier B.V. All rights reserved.

Characterization of selenium in ambient aerosols and primary emission sources.

Science.gov (United States)

De Santiago, Arlette; Longo, Amelia F; Ingall, Ellery D; Diaz, Julia M; King, Laura E; Lai, Barry; Weber, Rodney J; Russell, Armistead G; Oakes, Michelle

2014-08-19

Atmospheric selenium (Se) in aerosols was investigated using X-ray absorption near-edge structure (XANES) spectroscopy and X-ray fluorescence (XRF) microscopy. These techniques were used to determine the oxidation state and elemental associations of Se in common primary emission sources and ambient aerosols collected from the greater Atlanta area. In the majority of ambient aerosol and primary emission source samples, the spectroscopic patterns as well as the absence of elemental correlations suggest Se is in an elemental, organic, or oxide form. XRF microscopy revealed numerous Se-rich particles, or hotspots, accounting on average for ∼16% of the total Se in ambient aerosols. Hotspots contained primarily Se(0)/Se(-II). However, larger, bulk spectroscopic characterizations revealed Se(IV) as the dominant oxidation state in ambient aerosol, followed by Se(0)/Se(-II) and Se(VI). Se(IV) was the only observed oxidation state in gasoline, diesel, and coal fly ash, while biomass burning contained a combination of Se(0)/Se(-II) and Se(IV). Although the majority of Se in aerosols was in the most toxic form, the Se concentration is well below the California Environmental Protection Agency chronic exposure limit (∼20000 ng/m(3)).

Det Ambiente

DEFF Research Database (Denmark)

Schmidt, Ulrik

Det ambiente er iscenesættelsen af en karakteristisk sanseoplevelse, der er kendetegnet ved fornemmelsen af at være omgivet. I dag bliver begrebet om det ambiente mest anvendt i forbindelse med musikgenren ’ambient musik’. Det ambiente er dog ikke essentielt knyttet til det musikalske, men må...... forstås som et betydeligt bredere fænomen i den moderne æstetiske kultur, der spiller en væsentlig rolle i oplevelsen af moderne transportformer, arkitektur, film, lydkunst, installationskunst og digitale multimedieiscenesættelser. En forståelse af det ambiente er derfor centralt for forståelsen af en...... moderne æstetiseret oplevelseskultur i almindelighed. Da det ambiente ikke hidtil har været gjort til genstand for en mere indgående teoretisk behandling, er der dog stor usikkerhed omkring, hvad fænomenet overhovedet indebærer. Hovedformålet med Det ambiente – Sansning, medialisering, omgivelse er derfor...

Measurement of the atmospheric muon charge ratio with the OPERA detector

OpenAIRE

Mauri, Nicoletta

2011-01-01

The atmospheric muon charge ratio, defined as the number of positive over negative charged muons, is an interesting quantity for the study of high energy hadronic interactions in atmosphere and the nature of the primary cosmic rays. The measurement of the charge ratio in the TeV muon energy range allows to study the hadronic interactions in kinematic regions not yet explored at accelerators. The OPERA experiment is a hybrid electronic detector/emulsion apparatus, located in the undergroun...

Comparison of mesoscale model and tower measurements of surface fluxes during Winter Icing and Storms Program/Atmospheric Radiation Measurement 91

International Nuclear Information System (INIS)

Oncley, S.P.; Dudhia, J.

1994-01-01

This study is an evaluation of the ability of the Pennsylvania State University/National Center for Atmospheric Research (NCAR) mesoscale model (MM4) to determine surface fluxes to see if measured fluxes should be assimilated into model runs. Fluxes were compared from a high-resolution (5 km grid spacing) MM4 run during one day of the Winter Icing and Storms Programs/Atmospheric Radiation Measurement (WISP/ARM) experiment (over NE Colorado in winter 1991) with direct flux measurements made from a tower over a representative site by a three-dimensional sonic anemometer and fast response temperature and humidity sensors. This tower was part of the NCAR Atmosphere-Surface Turbulent Exchange Research (ASTER) facility. Also, mean values were compared to check whether any differences were due to the model parameterization or model variables

A measurement of summertime dry deposition of ambient air particulates and associated metallic pollutants in Central Taiwan.

Science.gov (United States)

Fang, Guor-Cheng; Chiang, Hung-Che; Chen, Yu-Cheng; Xiao, You-Fu; Wu, Chia-Ming; Kuo, Yu-Chen

2015-04-01

The purpose of this study is to characterize metallic elements associated with atmospheric particulate matter in the dry deposition plate, total suspended particulate, fine particles, and coarse particles at Taichung Harbor and Gong Ming Junior High School (airport) in central Taiwan at a sampling site from June 2013 to August 2013. The results indicated that: (1) the average concentrations of the metallic elements Cr and Cd were highest at the Gong Ming Junior High School (airport), and the average concentrations of the metallic elements Ni, Cu, and Pb were highest at the Taichung Harbor sampling site. (2) The high smelting industry density and export/import rate of heavily loaded cargos were the main reasons leading to these findings. (3) The average metallic element dry deposition and metallic element PM(2.5-10) all followed the order of Pb > Cr > Cu > Ni > Cd at the two sampling sites. However, the average metallic elements Cu and Pb were found to have the highest dry deposition velocities and concentrations in PM(2.5) for the two sampling sites in this study. (4) The correlation coefficients of ambient air particle dry deposition and concentration with wind speed at the airport were higher than those from the harbor sampling site. The wind and broad open spaces at Taichung Airport were the possible reasons for the increasing correlation coefficients for ambient air particle concentration and dry deposition with wind speed at the Taichung Airport sampling site.

Atmospheric Radiation Measurement Madden-Julian Oscillation Investigation Experiment Field Campaign Report

Energy Technology Data Exchange (ETDEWEB)

Long, Chuck [National Oceanic and Atmospheric Administration (NOAA), Boulder, CO (United States). Earth System Research Lab.

2016-07-01

Every 30–90 days during the Northern Hemisphere winter, the equatorial tropical atmosphere experiences pulses of extraordinarily strong deep convection and rainfall. This phenomenon is referred to as the Madden–Julian Oscillation, or MJO, named after the scientists who identified this cycle. The MJO significantly affects weather and rainfall patterns around the world (Zhang 2013). To improve predictions of the MJO—especially about how it forms and evolves throughout its lifecycle—an international group of scientists collected an unprecedented set of observations from the Indian Ocean and western Pacific region from October 2011 through March 2012 through several coordinated efforts. The coordinated field campaigns captured six distinct MJO cycles in the Indian Ocean. The rich set of observations capturing several MJO events from these efforts will be used for many years to study the physics of the MJO. Here we highlight early research results using data from the Atmospheric Radiation Measurement (ARM) Madden-Julian Oscillation Investigation Experiment (AMIE), sponsored by the U.S. Department of Energy (DOE) Atmospheric Radiation Measurement (ARM) Climate Research Facility.

Measurement of atmospheric neutrino composition with the IMB-3 detector

International Nuclear Information System (INIS)

Casper, D.; Becker-Szendy, R.; Bratton, C.B.; Cady, D.R.; Claus, R.; Dye, S.T.; Gajewski, W.; Goldhaber, M.; Haines, T.J.; Halverson, P.G.; Jones, T.W.; Kielczewska, D.; Kropp, W.R.; Learned, J.G.; LoSecco, J.M.; McGrew, C.; Matsuno, S.; Matthews, J.; Mudan, M.S.; Price, L.; Reines, F.; Schultz, J.; Sinclair, D.; Sobel, H.W.; Stone, J.L.; Sulak, L.R.; Svoboda, R.; Thornton, G.; van der Velde, J.C.; The University of Michigan, Ann Arbor, Michigan 48109 Brookhaven National; Laboratory, Upton, New York 11973; Boston University, Boston, Massachusetts 02215; The University of Hawaii, Honolulu, Hawaii 96822 University College, London, WC1E F6BT, United Kingdom; Warsaw University, Warsaw, Poland; Cleveland State University, Cleveland, Ohio 44115; The University of Notre Dame, Notre Dame, Indiana 46556; Lousiana State University, Baton Rouge, Lousisiana 70803; The University of Maryland, College Park, Maryland 20742)

1991-01-01

The atmospheric neutrino flux is measured using a 3.4-kt yr exposure of the IMB-3 detector. Single-ring events are classified as showering or nonshowering using the geometry of the Cerenkov pattern. A simulation of neutrino interactions and three models of atmospheric neutrino production are used to predict the composition of the sample. Showering-nonshowering character is strongly correlated with the flavor of the neutrino parent. In the lepton momentum range p<1500 MeV/c, we find that nonshowering events comprise [41±3±2syst]% of the total. The fraction expected is [51±5(syst)]%

Laser-induced breakdown spectroscopy for space exploration applications: Influence of the ambient pressure on the calibration curves prepared from soil and clay samples

International Nuclear Information System (INIS)

Salle, Beatrice; Cremers, David A.; Maurice, Sylvestre; Wiens, Roger C.

2005-01-01

Recently, there has been an increasing interest in the laser-induced breakdown spectroscopy (LIBS) technique for stand-off detection of geological samples for use on landers and rovers to Mars, and for other space applications. For space missions, LIBS analysis capabilities must be investigated and instrumental development is required to take into account constraints such as size, weight, power and the effect of environmental atmosphere (pressure and ambient gas) on flight instrument performance. In this paper, we study the in-situ LIBS method at reduced pressure (7 Torr CO 2 to simulate the Martian atmosphere) and near vacuum (50 mTorr in air to begin to simulate the Moon or asteroids' pressure) as well as at atmospheric pressure in air (for Earth conditions and comparison). Here in-situ corresponds to distances on the order of 150 mm in contrast to stand-off analysis at distance of many meters. We show the influence of the ambient pressure on the calibration curves prepared from certified soil and clay pellets. In order to detect simultaneously all the elements commonly observed in terrestrial soils, we used an Echelle spectrograph. The results are discussed in terms of calibration curves, measurement precision, plasma light collection system efficiency and matrix effects

Direct measurement of time dependent diffusion for Ag and Au under ambient conditions

Energy Technology Data Exchange (ETDEWEB)

Yoo, Pil Sun; Jo, Han Yeol; Kim, Tae Kyeong [Hankuk University of Foreign Studies, Yongin (Korea, Republic of)

2014-12-15

Time-dependent diffusion for Ag and Au metal atoms was measured using the scanning tunneling microscope break-junction technique in ambient conditions. We observed that Ag contacts do not form long single-atomic chains compared to Au contacts during the elongation of each metal electrode, and Ag atoms diffuse more quickly than Au atoms after metal contact rupture. This is consistent with previous results of molecular dynamic simulations. Further, we found a correlation between diffusion length and the evolution time on an atomic scale to reveal the time-dependent diffusion for Ag and Au metal atoms.

Folded tubular photometer for atmospheric measurements of NO2 and NO

Science.gov (United States)

Birks, John W.; Andersen, Peter C.; Williford, Craig J.; Turnipseed, Andrew A.; Strunk, Stanley E.; Ennis, Christine A.; Mattson, Erick

2018-05-01

We describe and characterize a modular folded tubular photometer for making direct measurements of the concentrations of nitrogen dioxide (NO2) and specify how this method could be extended to measure other pollutants such as sulfur dioxide (SO2), ozone (O3), and black carbon particulate matter. Direct absorbance measurements using this photometer can be made across the spectral range from the ultraviolet (UV) to the near infrared. The absorbance cell makes use of modular components (tubular detection cells and mirror cubes) that allow construction of path lengths of up to 2 m or more while maintaining low cell volumes. The long path lengths and low cell volumes enable sensitive detection of ambient air pollutants down to low part-per-billion levels for gas species and aerosol extinctions down to 1 Mm-1, corresponding to ˜ 0.1 µg m-3 for black carbon particulates. Pressure equalization throughout the stages of the absorbance measurement is shown to be critical to accurate measurements of analyte concentrations. The present paper describes the application of this photometer to direct measurements of nitrogen dioxide (NO2) and the incorporation of design features that also enable measurement of nitric oxide (NO) in the same instrument. Excellent agreement for ambient measurements along an urban roadside was found for both NO2 and NO measured by the folded tubular photometer compared to existing standard techniques. Compared to commonly used methods for measurements of NOx species, the advantages of this approach include (1) an absolute quantification for NO2 based on the Beer-Lambert law, thereby greatly reducing the frequency at which calibrations are required; (2) the direct measurement of NO2 concentration without prior conversion to NO as is required for the commonly used chemiluminescence method; (3) the use of modular components that allow construction of absorbance detection cells of varying lengths for extending the dynamic range of concentrations that can

Dioxin in the atmosphere of Denmark

Energy Technology Data Exchange (ETDEWEB)

Vikelsoee, J.; Hovmand, M.F.; Andersen, Helle V.; Bossi, R.; Johansen, Elsebeth; Chrillesen, M.A.

2006-03-15

Occurrence and geographical distribution of dioxin was investigated in air and deposition at selected locations in Denmark, three forest sites in the background area, a city site in Copenhagen and a village site. At two sites simultaneously determination of dioxins concentrations in the ambient atmosphere and bulk precipitation were carried out during a period of three years. (au)

Wide angle Michelson Doppler imaging interferometer. [measuring atmospheric emissions

Science.gov (United States)

Shepherd, G. G.

1980-01-01

The optical system, stepping control, phase and modulation depth, array detector, and directions sensor are described for a specialized type of Michelson interferometer which works at sufficiently high resolution to measure the line widths and Doppler shifts of naturally occurring atmospheric emissions. With its imaging capability, the instrument can potentially supply this data independently for each element of the 100 x 100 detector array. The experiment seeks: (1) to obtain vertical profiles of atmospheric winds and temperatures as functions of latitude by observing near the limb; (2) to acquire exploratory wind and temperature data on smaller scale structures in airglow irregularities and in auroral forms; and (3) to collaborate with other Spacelab experiments, such as barium cloud releases, in providing wind and temperature data.

Measurement of radioactivity in the atmosphere and pollution nearby an atomic centre

International Nuclear Information System (INIS)

Labeyrie, J.; Weill, J.

1955-01-01

The French Atomic Energy Commission (CEA) is particularly interested in studies on atmospheric radioactivity by reason of the necessity to control the atmosphere nearby nuclear plants as uranium mines, nuclear reactors and hot laboratories or radioactive materials treatment plants. Thus, the CEA developed different apparatus to control and monitor the atmosphere nearby its sites. These air monitors are essentially of two types: the first one, called 'Babar', monitors smokes, fogs and dusts, the second type is an ionization chamber and measures the concentration of radioactive gas in the air. The functioning and sensitivity of these two systems are discussed. (M.P.)

A microwave pressure sounder. [for remote measurement of atmospheric pressure

Science.gov (United States)

Peckham, G. E.; Flower, D. A.

1981-01-01

A technique for the remote measurement of atmospheric surface pressure will be described. Such measurements could be made from a satellite in polar orbit and would cover many areas for which conventional meteorological data are not available. An active microwave instrument is used to measure the strength of return echoes from the ocean surface at a number of frequencies near the 60 GHz oxygen absorption band. Factors which affect the accuracy with which surface pressure can be deduced from these measurements will be discussed and an instrument designed to test the method by making measurements from an aircraft will be described.

Determination of atmospheric aerosol properties over land using satellite measurements

NARCIS (Netherlands)

Kokhanovsky, A.A.; Leeuw, G. de

2009-01-01

Mostly, aerosol properties are poorly understood because the aerosol properties are very sparse. The first workshop on the determination of atmospheric aerosol properties over land using satellite measurements is convened in Bremen, Germany. In this workshop, the topics of discussions included a

Measurement of radioactive aerosols as an original indicator of atmospheric pollution in urban areas

International Nuclear Information System (INIS)

Le Petit, G.; Millies-Lacroix, J.-C.; Simon, F.

1998-01-01

The Service Radioanalyses, Chimie et Environnement (Departement Analyses Surveillance de l'Environnement) of the French Atomic Energy Commission, located in suburban Paris, has for many years been conducting atmospheric radioactivity measurements. Since 1994, the laboratory has been using high volume air samplers equipped with filters for the weekly collection of atmospheric aerosols at a mean rate of about 600 m 3 .h -1 . The polypropylene filters, with a collection efficiency in excess of 93%, are compacted after sampling. The atmospheric radioactivity is measured by HP Ge gamma spectrometry after decay of short-lived natural relationship products. A study conducted in 1996 shows good correlation between the evolution with time of some of the indicators routinely used by AIRPARIF, the organization in charge of monitoring of the air quality in the Ile-de-France region, to measure atmospheric pollution in the Paris area (SO 2 , NO) and that related to radioactivity of terrestrial ( 210 Pb, 40 K) and anthropogenic ( 137 Cs) origin, as well as the amount of aerosols collected. Further, the distribution in time of the atmospheric radioactivity of cosmogenic origin ( 7 Be) shows a yearly evolution somewhat similar to that observed with ozone. (author). 16 refs., 21 figs., 1 tab

On the Effects of Atmospheric Particles Contamination and Humidity on Tin Corrosion

DEFF Research Database (Denmark)

D’Angelo, L.; Verdingovas, V.; Ferrero, L.

2017-01-01

The effects of hygroscopic atmospheric particles are investigated in relation to the corrosion of tin. Surface insulation resistance test boards were directly contaminated both with ambient particles sampled in the field at Milan, Italy, and with pure saline particles generated in the laboratory....... An innovative particle deposition device was used to uniformly coat circular spots on to the test board surfaces. Deliquescence and crystallization of the water-soluble compounds were detected by observing the impedance response to varying relative humidity (RH) conditions with a gradual and continuous ramps....... The effects of the adsorption/desorption kinetics and of the temperature on the deliquescence and crystallization RH values were also investigated. Leakage current measurements at 5-V dc highlighted the ability of atmospheric particles to promote corrosion and electrochemical migration at RH levels far below...

Evaluation of the use of bioethanol fuelled buses based on ambient air pollution screening and on-road measurements.

Science.gov (United States)

López-Aparicio, S; Hak, C

2013-05-01

Mitigation measures to reduce greenhouse gas emissions may have adverse effects on urban air quality and human exposure to harmful pollutants. The use of bioethanol fuelled vehicles is increasing worldwide and may create new undesired pollution effects. Different measurement campaigns were performed in a pilot study to contribute to the understanding of the consequences associated with the use of bioethanol blended fuel (E95) on a series of pollutants. Ambient screening measurements of NO2, O3, acetic acid, formaldehyde and acetaldehyde were performed at different urban locations, exposed and not exposed to the circulation of bioethanol buses. In addition, volatile organic compounds were measured at the exhaust pipe of a bioethanol fuelled bus, both under idling conditions (carbonyls; DNPH cartridge) and under on-road driving conditions applying online monitoring (PTR-TOF). Higher ambient acetaldehyde values were measured at locations exposed to bioethanol fuelled buses than at locations not exposed, and very high acetaldehyde and acetic acid values were measured from the exhaust pipe during driving conditions (acetaldehyde>150 ppm; acetic acid ≈ 20-30 ppm) and modelled at close distance to the bioethanol bus. Human exposure to high concentration of acetaldehyde is expected, and it may involve a significantly increased chance in developing cancer. The high concentration of acetic acid will involve odour annoyance and significant material degradation or corrosion. Copyright © 2013 Elsevier B.V. All rights reserved.

Measurement of interferences associated with the detection of the hydroperoxy radical in the atmosphere using laser-induced fluorescence

Science.gov (United States)

Lew, Michelle M.; Dusanter, Sebastien; Stevens, Philip S.

2018-01-01

One technique used to measure concentrations of the hydroperoxy radical (HO2) in the atmosphere involves chemically converting it to OH by addition of NO and subsequent detection of OH. However, some organic peroxy radicals (RO2) can also be rapidly converted to HO2 (and subsequently OH) in the presence of NO, interfering with measurements of ambient HO2 radical concentrations. This interference must be characterized for each instrument to determine to what extent various RO2 radicals interfere with measurements of HO2 and to assess the impact of this interference on past measurements. The efficiency of RO2-to-HO2 conversion for the Indiana University laser-induced fluorescence-fluorescence assay by gas expansion (IU-FAGE) instrument was measured for a variety of RO2 radicals. Known quantities of OH and HO2 radicals were produced from the photolysis of water vapor at 184.9 nm, and RO2 radicals were produced by the reaction of several volatile organic compounds (VOCs) with OH. The conversion efficiency of RO2 radicals to HO2 was measured when NO was added to the sampling cell for conditions employed during several previous field campaigns. For these conditions, approximately 80 % of alkene-derived RO2 radicals and 20 % of alkane-derived RO2 radicals were converted to HO2. Based on these measurements, interferences from various RO2 radicals contributed to approximately 35 % of the measured HO2 signal during the Mexico City Metropolitan Area (MCMA) 2006 campaign (MCMA-2006), where the measured VOCs consisted of a mixture of saturated and unsaturated species. However, this interference can contribute more significantly to the measured HO2 signal in forested environments dominated by unsaturated biogenic emissions such as isoprene.

Changes in concentration and (delta) 13C value of dissolved CH4, CO2 and organic carbon in rice paddies under ambient and elevated concentrations of atmospheric CO2

International Nuclear Information System (INIS)

Weiguo Cheng; Yagi, Kazuyuki; Sakai, Hidemitsu; Hua Xu; Kobayashi, Kazuhiko

2005-01-01

Changes in concentration and (delta) 13 C value of dissolved CH 4 , CO 2 and organic carbon (DOC) in floodwater and soil solution from a Japanese rice paddy were studied under ambient and elevated concentrations of atmospheric CO 2 in controlled environment chambers. The concentrations of dissolved CH 4 in floodwater increased with rice growth (with some fluctuation), while the concentrations of CO 2 remained between 2.9 to 4.4 and 4.2 to 5.8 μg C mL -1 under conditions of ambient and elevated CO 2 concentration, respectively. The amount of CH 4 dissolved in soil solution under elevated CO 2 levels was significantly lower than under ambient CO 2 in the tillering stage, implying that the elevated CO 2 treatment accelerated CH 4 oxidation during the early stage of growth. However, during later stages of growth, production of CH 4 increased and the amount of CH 4 dissolved in soil solution under elevated CO 2 levels was, on average, greater than that under ambient CO 2 conditions. Significant correlation existed among the (delta) 13 C values of dissolved CH 4 , CO 2 , and DOC in floodwater (except for the samples taken immediately after pulse feeding with 13 C enriched CO 2 ), indicating that the origins and cycling of CH 4 , CO 2 and DOC were related. There were also significant correlations among the (delta) 13 C values of CH 4 , CO 2 and DOC in the soil solution. The turnover rate of CO 2 in soil solution was most rapid in the panicle formation stage of rice growth and that of CH 4 fastest in the grain filling stage. (Author)

Simulation of microbubble response to ambient pressure changes

DEFF Research Database (Denmark)

Andersen, Klaus Scheldrup; Jensen, Jørgen Arendt

2008-01-01

The theory on microbubbles clearly indicates a relation between the ambient pressure and the acoustic behavior of the bubble. The purpose of this study was to optimize the sensitivity of ambient pressure measurements, using the subharmonic component, through microbubble response simulations....... The behaviour of two different contrast agents was investigated as a function of driving pulse and ambient overpressure, pov. Simulations of Levovist using a rectangular driving pulse show an almost linear reduction in the subharmonic component as pov is increased. For a 20 cycles driving pulse, a reduction...... is not completely linear as a function of the ambient pressure....

Measurement of Ozone Production Sensor

Directory of Open Access Journals (Sweden)

M. Cazorla

2010-05-01

Full Text Available A new ambient air monitor, the Measurement of Ozone Production Sensor (MOPS, measures directly the rate of ozone production in the atmosphere. The sensor consists of two 11.3 L environmental chambers made of UV-transmitting Teflon film, a unit to convert NO₂ to O₃, and a modified ozone monitor. In the sample chamber, flowing ambient air is exposed to the sunlight so that ozone is produced just as it is in the atmosphere. In the second chamber, called the reference chamber, a UV-blocking film over the Teflon film prevents ozone formation but allows other processes to occur as they do in the sample chamber. The air flows that exit the two chambers are sampled by an ozone monitor operating in differential mode so that the difference between the two ozone signals, divided by the exposure time in the chambers, gives the ozone production rate. High-efficiency conversion of NO₂ to O₃ prior to detection in the ozone monitor accounts for differences in the NO_x photostationary state that can occur in the two chambers. The MOPS measures the ozone production rate, but with the addition of NO to the sampled air flow, the MOPS can be used to study the sensitivity of ozone production to NO. Preliminary studies with the MOPS on the campus of the Pennsylvania State University show the potential of this new technique.

Temporal and spatial dynamics of laser-induced aluminum plasma in argon background at atmospheric pressure: Interplay with the ambient gas

International Nuclear Information System (INIS)

Ma, Q.L.; Motto-Ros, V.; Lei, W.Q.; Boueri, M.; Bai, X.S.; Zheng, L.J.; Zeng, H.P.; Yu, J.

2010-01-01

Laser ablation in background gas implies supplementary complexities with respect to what happens in the vacuum. It is however essential to understand in detail the involved mechanisms for a number of applications requiring the ablation to be performed in an ambient gas at relative high pressure, such as pulsed-laser deposition, or laser-induced breakdown spectroscopy. In this paper, the expansion of a vapor plume ablated from an aluminum target into an argon gas at atmospheric pressure is experimentally investigated using time- and space-resolved emission spectroscopy. The obtained results provide a detailed description of the interplay between the vapor and the gas. The electron density, the temperature and the number densities (and therefore the partial pressures) of aluminum vapor and argon gas have been measured in and surrounding the vapor plume. Our observations show a confinement of the vapor plume by the gas, which is expected as predicted by the usual hydrodynamics models. The result is a plasma core with quite uniform distributions in electron density, temperature and number densities. Such plasma core presents an ideal emission source for spectroscopic applications. It is however evidenced by our observations that a large amount of argon is mixed into the aluminum plume in the plasma core, which invalidates in the experimental conditions that we used, the hydrodynamic 'piston' model where the background gas is pushed out by the shock wave surrounding the vapor plume. Instead, other mechanisms such as laser-supported detonation wave should play important roles in the early stage of the expansion of the plasma for the determination of its morphology at longer delays.

Atmospheric radiation measurement program facilities newsletter, September 2001.; TOPICAL

International Nuclear Information System (INIS)

Holdridge, D. J.

2001-01-01

Our Changing Climate-Is our climate really changing? How do we measure climate change? How can we predict what Earth's climate will be like for generations to come? One focus of the Atmospheric Radiation Measurement (ARM) Program is to improve scientific climate models enough to achieve reliable regional prediction of future climate. According to the Environmental Protection Agency (EPA), the global mean surface temperature has increased by 0.5-1.0 F since the late 19th century. The 20th century's 10 warmest years all occurred in the last 15 years of the century, with 1998 being the warmest year of record. The global mean surface temperature is measured by a network of temperature-sensing instruments distributed around the world, including ships, ocean buoys, and weather stations on land. The data from this network are retrieved and analyzed by various organizations, including the National Aeronautics and Space Administration, the National Oceanic and Atmospheric Administration, and the World Meteorological Organization. Worldwide temperature records date back to 1860. To reconstruct Earth's temperature history before 1860, scientists use limited temperature records, along with proxy indicators such as tree rings, pollen records, and analysis of air frozen in ancient ice. The solar energy received from the sun drives Earth's weather and climate. Some of this energy is reflected and filtered by the atmosphere, but most is absorbed by Earth's surface. The absorbed solar radiation warms the surface and is re-radiated as heat energy into the atmosphere. Some atmospheric gases, called greenhouse gases, trap some of the re-emitted heat, keeping the surface temperature regulated and suitable for sustaining life. Although the greenhouse effect is natural, some evidence indicates that human activities are producing increased levels of some greenhouse gases such as carbon dioxide, methane, and nitrous oxide. Scientists believe that the combustion of fossil fuels is

The design of laser atmosphere transmission characteristic measurement system based on virtual instrument

Science.gov (United States)

Zhang, Laixian; Sun, Huayan; Xu, Jiawen

2010-10-01

The laser atmosphere transmission characteristic affects the use of laser in engineering greatly. This paper designed a laser atmosphere transmission characteristic measurement system based on LabVIEW software, a product of NI. The system acquires laser spacial distribution by means of controlling NI image acquisition card and CCD through PCI, controls oscillograph to acquire laser time domain distribution through Ethernet and controls power meter to acquire energy of laser through RS-232. It processes the data acquired and analyses the laser atmosphere transmission characteristic using Matlab, which is powerful in data processing, through software interface. It provided a new way to study the laser atmosphere transmission characteristic.

Estimation of Atmospheric Path Delays in TerraSAR-X Data using Models vs. Measurements

Directory of Open Access Journals (Sweden)

Donat Perler

2008-12-01

Full Text Available Spaceborne synthetic aperture radar (SAR measurements of the Earth’s surface depend on electromagnetic waves that are subject to atmospheric path delays, in turn affecting geolocation accuracy. The atmosphere influences radar signal propagation by modifying its velocity and direction, effects which can be modeled. We use TerraSAR-X (TSX data to investigate improvements in the knowledge of the scene geometry. To precisely estimate atmospheric path delays, we analyse the signal return of four corner reflectors with accurately surveyed positions (based on differential GPS, placed at different altitudes yet with nearly identical slant ranges to the sensor. The comparison of multiple measurements with path delay models under these geometric conditions also makes it possible to evaluate the corrections for the atmospheric path delay made by the TerraSAR processor and to propose possible improvements.

Association of atmospheric concentrations of polycyclic aromatic hydrocarbons with their urinary metabolites in children and adolescents.

Science.gov (United States)

Poursafa, Parinaz; Amin, Mohammad Mehdi; Hajizadeh, Yaghoub; Mansourian, Marjan; Pourzamani, Hamidreza; Ebrahim, Karim; Sadeghian, Babak; Kelishadi, Roya

2017-07-01

This study aims to determine the atmospheric concentrations of particulate matter 2.5 (PM 2.5 )-bounded polycyclic aromatic hydrocarbons (PAHs) and their association with their urinary metabolites in children and adolescents. This study was conducted from October 2014 to March 2016 in Isfahan, Iran. We measured 16 species of PAHs bounded to PM 2.5 by gas chromatography mass spectrometry (GC/MS) from 7 parts of the city. Moreover, PAH urinary metabolites were measured in 186 children and adolescents, randomly selected from households. Urinary metabolites consisted of 1-hydroxy naphthalene (1-naphthol), 2-hydroxy naphthalene (2-naphthol), 9-hydroxy phenanthrene (9-phenanthrol), and 1-hydroxy pyrene using GC/MS. Considering the short half-lives of PAHs, we measured the metabolites twice with 4 to 6 months of time interval. We found that the ambient concentrations of PAHs were significantly associated with their urinary metabolites. 1-hydroxy naphthalene and 2-hydroxy naphthalene concentrations showed an increase of 1.049 (95% CI: 1.030, 1.069) and 1.047 (95% CI: 1.025, 1.066) for each unit increase (1 ng/m 3 ) in ambient naphthalene. Similarly, 1-hydroxy pyrene showed an increase of 1.009 (95% CI: 1.006-1.011) for each unit increase (1 ng/m 3 ) in ambient pyrene concentration after adjustment for body mass index, physical activity level, urinary creatinine, age, and sex. The association of urinary 9-hydroxyphenanthrene and ambient phenantherene was significant in the crude model; however after adjustment for the abovementioned covariates, it was no more significant. We found significant correlations between exposure to ambient PM 2.5 -bounded PAHs and their urinary excretion. Considering the adverse health effects of PAHs in the pediatric age group, biomonitoring of PAHs should be underscored; preventive measures need to be intensified.

Vertical Sampling Scales for Atmospheric Boundary Layer Measurements from Small Unmanned Aircraft Systems (sUAS

Directory of Open Access Journals (Sweden)

Benjamin L. Hemingway

2017-09-01

Full Text Available The lowest portion of the Earth’s atmosphere, known as the atmospheric boundary layer (ABL, plays an important role in the formation of weather events. Simple meteorological measurements collected from within the ABL, such as temperature, pressure, humidity, and wind velocity, are key to understanding the exchange of energy within this region, but conventional surveillance techniques such as towers, radar, weather balloons, and satellites do not provide adequate spatial and/or temporal coverage for monitoring weather events. Small unmanned aircraft, or aerial, systems (sUAS provide a versatile, dynamic platform for atmospheric sensing that can provide higher spatio-temporal sampling frequencies than available through most satellite sensing methods. They are also able to sense portions of the atmosphere that cannot be measured from ground-based radar, weather stations, or weather balloons and have the potential to fill gaps in atmospheric sampling. However, research on the vertical sampling scales for collecting atmospheric measurements from sUAS and the variabilities of these scales across atmospheric phenomena (e.g., temperature and humidity is needed. The objective of this study is to use variogram analysis, a common geostatistical technique, to determine optimal spatial sampling scales for two atmospheric variables (temperature and relative humidity captured from sUAS. Results show that vertical sampling scales of approximately 3 m for temperature and 1.5–2 m for relative humidity were sufficient to capture the spatial structure of these phenomena under the conditions tested. Future work is needed to model these scales across the entire ABL as well as under variable conditions.

Electron density measurement of non-equilibrium atmospheric pressure plasma using dispersion interferometer

Science.gov (United States)

Yoshimura, Shinji; Kasahara, Hiroshi; Akiyama, Tsuyoshi

2017-10-01

Medical applications of non-equilibrium atmospheric plasmas have recently been attracting a great deal of attention, where many types of plasma sources have been developed to meet the purposes. For example, plasma-activated medium (PAM), which is now being studied for cancer treatment, has been produced by irradiating non-equilibrium atmospheric pressure plasma with ultrahigh electron density to a culture medium. Meanwhile, in order to measure electron density in magnetic confinement plasmas, a CO2 laser dispersion interferometer has been developed and installed on the Large Helical Device (LHD) at the National Institute for Fusion Science, Japan. The dispersion interferometer has advantages that the measurement is insensitive to mechanical vibrations and changes in neutral gas density. Taking advantage of these properties, we applied the dispersion interferometer to electron density diagnostics of atmospheric pressure plasmas produced by the NU-Global HUMAP-WSAP-50 device, which is used for producing PAM. This study was supported by the Grant of Joint Research by the National Institutes of Natural Sciences (NINS).

Broadband Outdoor Radiometer Calibration Process for the Atmospheric Radiation Measurement Program

Energy Technology Data Exchange (ETDEWEB)

Dooraghi, Michael [National Renewable Energy Lab. (NREL), Golden, CO (United States)

2015-09-01

The Atmospheric Radiation Measurement program (ARM) maintains a fleet of monitoring stations to aid in the improved scientific understanding of the basic physics related to radiative feedback processes in the atmosphere, particularly the interactions among clouds and aerosols. ARM obtains continuous measurements and conducts field campaigns to provide data products that aid in the improvement and further development of climate models. All of the measurement campaigns include a suite of solar measurements. The Solar Radiation Research Laboratory at the National Renewable Energy Laboratory supports ARM's full suite of stations in a number of ways, including troubleshooting issues that arise as part of the data-quality reviews; managing engineering changes to the standard setup; and providing calibration services and assistance to the full fleet of solar-related instruments, including pyranometers, pyrgeometers, pyrheliometers, as well as the temperature/relative humidity probes, multimeters, and data acquisition systems that are used in the calibrations performed at the Southern Great Plains Radiometer Calibration Facility. This paper discusses all aspects related to the support provided to the calibration of the instruments in the solar monitoring fleet.

Performances of an atmospheric tritium sampler and its application

International Nuclear Information System (INIS)

Inoue, Yoshikazu; Kahn, B.; Carter, M.W.

1983-01-01

A sampling system for atmospheric tritium in the form of water vapor, hydrogen and hydrocarbons was designed and built. The air was passed first through molecular sieve which adsorbed water vapor, then over palladium catalyst which oxidized hydrogen and adsorbed resulting water in situ, and finally over hot Hopcalite catalyst, which oxidized hydrocarbons and the resulting water was adsorbed on a following molecular sieve column. Three water samples were extracted from adsorbers and their tritium contents were measured by liquid scintillation counting. Performances of this sampler were examined for retrieval of tritiated water from molecular sieve, oxidation of hydrogen on palladium catalyst and oxidation of methane on Hopcalite. The portable sampler was applied to analyze tritium in a duct air of a heavy water moderated research reactor. More than 99% of total tritium was in vapor form. Trace amounts of tritiated hydrogen and hydrocarbon were also detected. This tritium sampler is applicable to detect all of atmospheric tritium as high as ten times of ambient levels. (author)

Atmospheric CO2 measurements with a 2-μm DIAL instrument

Science.gov (United States)

Cadiou, Erwan; Dherbecourt*, Jean-Baptiste; Gorju, Guillaume; Melkonian, Jean-Michel; Godard, Antoine; Pelon, Jacques; Raybaut, Myriam

2018-04-01

We report on ground-based atmospheric concentration measurements of carbon dioxide, using a pulsed direct detection differential absorption lidar operating at 2051 nm. The transmitter is based on a tunable parametric source emitting 10-mJ energy, 10-ns duration Fourier-limited pulses. Range resolved concentration measurements have been carried out on the aerosol back-scattered signal. Cloud signals have been used to get long range integrated-path measurements.

Temporal evolution of main ambient PM2. 5 sources in Santiago, Chile, from 1998 to 2012

Directory of Open Access Journals (Sweden)

F. Barraza

2017-08-01

Full Text Available The inhabitants of Santiago, Chile have been exposed to harmful levels of air pollutants for decades. The city's poor air quality is a result of steady economic growth, and stable atmospheric conditions adverse to mixing and ventilation that favor the formation of oxidants and secondary aerosols. Identifying and quantifying the sources that contribute to the ambient levels of pollutants is key for designing adequate mitigation measures. Estimating the evolution of source contributions to ambient pollution levels is also paramount to evaluating the effectiveness of pollution reduction measures that have been implemented in recent decades. Here, we quantify the main sources that have contributed to fine particulate matter (PM2. 5 between April 1998 and August 2012 in downtown Santiago by using two different source-receptor models (PMF 5.0 and UNMIX 6.0 that were applied to elemental measurements of 1243 24 h filter samples of ambient PM2.5. PMF resolved six sources that contributed to ambient PM2. 5, with UNMIX producing similar results: motor vehicles (37.3 ± 1.1 %, industrial sources (18.5 ± 1.3 %, copper smelters (14.4 ± 0.8 %, wood burning (12.3 ± 1.0 %, coastal sources (9.5 ± 0.7 % and urban dust (3.0 ± 1.2 %. Our results show that over the 15 years analyzed here, four of the resolved sources significantly decreased [95 % confidence interval]: motor vehicles 21.3 % [2.6, 36.5], industrial sources 39.3 % [28.6, 48.4], copper smelters 81.5 % [75.5, 85.9], and coastal sources 58.9 % [38.5, 72.5], while wood burning did not significantly change and urban dust increased by 72 % [48.9, 99.9]. These changes are consistent with emission reduction measures, such as improved vehicle emission standards, cleaner smelting technology, introduction of low-sulfur diesel for vehicles and natural gas for industrial processes, public transport improvements, etc. However, it is also apparent that the

Comparison of OH reactivity measurements in the atmospheric simulation chamber SAPHIR

Directory of Open Access Journals (Sweden)

H. Fuchs

2017-10-01

Full Text Available Hydroxyl (OH radical reactivity (kOH has been measured for 18 years with different measurement techniques. In order to compare the performances of instruments deployed in the field, two campaigns were conducted performing experiments in the atmospheric simulation chamber SAPHIR at Forschungszentrum Jülich in October 2015 and April 2016. Chemical conditions were chosen either to be representative of the atmosphere or to test potential limitations of instruments. All types of instruments that are currently used for atmospheric measurements were used in one of the two campaigns. The results of these campaigns demonstrate that OH reactivity can be accurately measured for a wide range of atmospherically relevant chemical conditions (e.g. water vapour, nitrogen oxides, various organic compounds by all instruments. The precision of the measurements (limit of detection  < 1 s−1 at a time resolution of 30 s to a few minutes is higher for instruments directly detecting hydroxyl radicals, whereas the indirect comparative reactivity method (CRM has a higher limit of detection of 2 s−1 at a time resolution of 10 to 15 min. The performances of the instruments were systematically tested by stepwise increasing, for example, the concentrations of carbon monoxide (CO, water vapour or nitric oxide (NO. In further experiments, mixtures of organic reactants were injected into the chamber to simulate urban and forested environments. Overall, the results show that the instruments are capable of measuring OH reactivity in the presence of CO, alkanes, alkenes and aromatic compounds. The transmission efficiency in Teflon inlet lines could have introduced systematic errors in measurements for low-volatile organic compounds in some instruments. CRM instruments exhibited a larger scatter in the data compared to the other instruments. The largest differences to reference measurements or to calculated reactivity were observed by CRM instruments in

Atmospheric radiation measurement program facilities newsletter, April 2001.; TOPICAL

International Nuclear Information System (INIS)

Holdridge, D. J.

2001-01-01

Intensive Observation Period Projects Scheduled-Several IOP projects have been scheduled for the SGP CART site this spring. These projects either have already begun or will begin shortly. Radiosondes-The RS-90 Transition IOP is currently under way. The RS-90 model radiosonde is gradually replacing the older RS-80 model. Radiosondes are instrument packages attached to and launched by weather balloons. The instruments measure atmospheric pressure, temperature, and relative humidity as the balloon rises through the air. The new RS-90 model is a high-performance radiosonde with fast-response sensors capable of providing data for each variable every second. The relatively environmentally friendly package is constructed of cardboard and steel rather than Styrofoam, and it has a water-activated battery that contains no toxic substances. The RS-90 Transition IOP is taking place during April. Operators will launch both the old RS-80 and the new RS-90 radiosondes simultaneously once each day to obtain duplicate vertical profiles of the atmosphere for comparison. This procedure will also allow data users to test the output from the old and new radiosondes in models. Narrow Field of View (NFOV) Solar Spectrometer Cloud Optical Depth Retrieval Campaign-The NFOV IOP is scheduled to take place on May 7-August 31, 2001. A researcher from Pennsylvania State University will be deploying a dual-spectrometer instrument that measures the hemispheric flux and zenith NFOV radiance over a wavelength range of 300- 1000 nanometers. (One nanometer equals 1 billionth of a meter or 0.000000039 inches.) This wavelength range includes the ultraviolet, visible, and near-infrared spectra. These measurements are used to estimate cloud optical depth-a quantity related to the amount of solar radiation intercepted by a cloud-for broken cloud fields over vegetated surfaces. The IOP measurements will be compared with optical depth measurements made by SGP instruments. Precision Gas Sampling (PGS

Atmospheric Radiation Measurement Program Plan

International Nuclear Information System (INIS)

1990-02-01

In order to understand energy's role in anthropogenic global climate change, significant reliance is being placed on General Circulation Models (GCMs). A major goal of the Department is to foster the development of GCMs capable of predicting the timing and magnitude of greenhouse gas-induced global warming and the regional effects of such warming. DOE research has revealed that cloud radiative feedback is the single most important effect determining the magnitude of possible climate responses to human activity. However, cloud radiative forcing and feedbacks are not understood at the levels needed for reliable climate prediction. The Atmospheric Radiation Measurement (ARM) Program will contribute to the DOE goal by improving the treatment of cloud radiative forcing and feedbacks in GCMs. Two issues will be addressed: the radiation budget and its spectral dependence and the radiative and other properties of clouds. Understanding cloud properties and how to predict them is critical because cloud properties may very well change as climate changes. The experimental objective of the ARM Program is to characterize empirically the radiative processes in the Earth's atmosphere with improved resolution and accuracy. A key to this characterization is the effective treatment of cloud formation and cloud properties in GCMs. Through this characterization of radiative properties, it will be possible to understand both the forcing and feedback effects. GCM modelers will then be able to better identify the best approaches to improved parameterizations of radiative transfer effects. This is expected to greatly improve the accuracy of long-term, GCM predictions and the efficacy of those predictions at the important regional scale, as the research community and DOE attempt to understand the effects of greenhouse gas emissions on the Earth's climate. 153 refs., 24 figs., 6 tabs

On the choice of retrieval variables in the inversion of remotely sensed atmospheric measurements.

Science.gov (United States)

Ridolfi, Marco; Sgheri, Luca

2013-05-06

In this paper we introduce new variables that can be used to retrieve the atmospheric continuum emission in the inversion of remote sensing measurements. This modification tackles the so-called sloppy model problem. We test this approach on an extensive set of real measurements from the Michelson Interferometer for Passive Atmospheric Sounding. The newly introduced variables permit to achieve a more stable inversion and a smaller value of the minimum of the cost function.

Dissolved atmospheric gas in xylem sap measured with membrane inlet mass spectrometry.

Science.gov (United States)

Schenk, H Jochen; Espino, Susana; Visser, Ate; Esser, Bradley K

2016-04-01

A new method is described for measuring dissolved gas concentrations in small volumes of xylem sap using membrane inlet mass spectrometry. The technique can be used to determine concentrations of atmospheric gases, such as argon, as reported here, or for any dissolved gases and their isotopes for a variety of applications, such as rapid detection of trace gases from groundwater only hours after they were taken up by trees and rooting depth estimation. Atmospheric gas content in xylem sap directly affects the conditions and mechanisms that allow for gas removal from xylem embolisms, because gas can dissolve into saturated or supersaturated sap only under gas pressure that is above atmospheric pressure. The method was tested for red trumpet vine, Distictis buccinatoria (Bignoniaceae), by measuring atmospheric gas concentrations in sap collected at times of minimum and maximum daily temperature and during temperature increase and decline. Mean argon concentration in xylem sap did not differ significantly from saturation levels for the temperature and pressure conditions at any time of collection, but more than 40% of all samples were supersaturated, especially during the warm parts of day. There was no significant diurnal pattern, due to high variability between samples. © 2015 John Wiley & Sons Ltd.

110. PTB seminar: Dose rate measurements of ionizing radiation in the range of natural ambient radiation. Proceedings

International Nuclear Information System (INIS)

Lauterbach, U.; Pessara, W.; Woehler-Figgen, S.

1997-12-01

Measuring instruments for radiation dose measurement in the range of natural ambient radiation are not subject to legal obligations for calibration and the PTB received numerous requests in the past, asking for measures to be taken in order to ensure reliability of measuring results in this range of radiation. This has induced PTB to organise the seminar, intended to present the current status of measuring technology in this field, reveal problems encountered in practical applications, and discuss suitable ction for quality assurance. The papers of the seminar report the measuring performance and capabilities of the available instruments, results of comparative analyses of measurements, and resulting proposed action for quality assurance. Discussions concluding the sessions are also presented in the processdings volume. (orig./CB) [de

Measurement of Spatial Coherence of Light Propagating in a Turbulent Atmosphere

Directory of Open Access Journals (Sweden)

P. Barcik

2013-04-01

Full Text Available A lot of issues have to be taken into account when designing a reliable free space optical communication link. Among these are e.g.,beam wander, fluctuation of optical intensity and loss of spatial coherence that are caused by atmospheric turbulence. This paper presents experimental measurements of spatial coherence of a laser beam. The experimental setup is based on Young's double pinhole experiment. Fringe patterns under atmospheric turbulence for four different pinhole separations are presented. From these fringe patterns, visibility is determined and the coherence radius is estimated.

Ambient temperature and cardiovascular biomarkers in a repeated-measure study in healthy adults: A novel biomarker index approach.

Science.gov (United States)

Wu, Shaowei; Yang, Di; Pan, Lu; Shan, Jiao; Li, Hongyu; Wei, Hongying; Wang, Bin; Huang, Jing; Baccarelli, Andrea A; Shima, Masayuki; Deng, Furong; Guo, Xinbiao

2017-07-01

Associations of ambient temperature with cardiovascular morbidity and mortality have been well documented in numerous epidemiological studies, but the underlying pathways remain unclear. We investigated whether systemic inflammation, coagulation, systemic oxidative stress, antioxidant activity and endothelial function may be the mechanistic pathways associated with ambient temperature. Forty study participants underwent repeated blood collections for 12 times in Beijing, China in 2010-2011. Ambient temperature and air pollution data were measured in central monitors close to student residences. We created five indices as the sum of weighted biomarker percentiles to represent the overall levels of 15 cardiovascular biomarkers in five pathways (systemic inflammation: hs-CRP, TNF-α and fibrinogen; coagulation: fibrinogen, PAI-1, tPA, vWF and sP-selectin; systemic oxidative stress: Ox-LDL and sCD36: antioxidant activity: EC-SOD and GPX1; and endothelial function: ET-1, E-selectin, ICAM-1 and VCAM-1). We used generalized mixed-effects models to estimate temperature effects controlling for air pollution and other covariates. There were significant decreasing trends in the adjusted means of biomarker indices over the lowest to the highest quartiles of daily temperatures before blood collection. A 10°C decrease at 2-d average daily temperature were associated with increases of 2.5% [95% confidence interval (CI): 0.7, 4.2], 1.6% (95% CI: 0.1, 3.1), 2.7% (95% CI: 0.5, 4.8), 5.5% (95% CI: 3.8, 7.3) and 2.0% (95% CI: 0.3, 3.8) in the indices for systemic inflammation, coagulation, systemic oxidative stress, antioxidant activity and endothelial function, respectively. In contrast, the associations between ambient temperature and individual biomarkers had substantial variation in magnitude and strength. The altered cardiovascular biomarker profiles in healthy adults associated with ambient temperature changes may help explain the temperature-related cardiovascular morbidity

Advances of study on atmospheric methane oxidation (consumption) in forest soil

Institute of Scientific and Technical Information of China (English)

WANG Chen-rui; SHI Yi; YANG Xiao-ming; WU Jie; YUE Jin

2003-01-01

Next to CO2, methane (CH4) is the second important contributor to global warming in the atmosphere and global atmospheric CH4 budget depends on both CH4 sources and sinks. Unsaturated soil is known as a unique sink for atmospheric CH4 in terrestrial ecosystem. Many comparison studies proved that forest soil had the biggest capacity of oxidizing atmospheric CH4 in various unsaturated soils. However, up to now, there is not an overall review in the aspect of atmospheric CH4 oxidation (consumption) in forest soil. This paper analyzed advances of studies on the mechanism of atmospheric CH4 oxidation, and related natural factors (Soil physical and chemical characters, temperature and moisture, ambient main greenhouse gases concentrations, tree species, and forest fire) and anthropogenic factors (forest clear-cutting and thinning, fertilization, exogenous aluminum salts and atmospheric deposition, adding biocides, and switch of forest land use) in forest soils. It was believed that CH4 consumption rate by forest soil was limited by diffusion and sensitive to changes in water status and temperature of soil. CH4 oxidation was also particularly sensitive to soil C/N, Ambient CO2, CH4 and N2O concentrations, tree species and forest fire. In most cases, anthropogenic disturbances will decrease atmospheric CH4 oxidation, thus resulting in the elevating of atmospheric CH4. Finally, the author pointed out that our knowledge of atmospheric CH4 oxidation (consumption) in forest soil was insufficient. In order to evaluate the contribution of forest soils to atmospheric CH4 oxidation and the role of forest played in the process of global environmental change, and to forecast the trends of global warming exactly, more researchers need to studies further on CH4 oxidation in various forest soils of different areas.

Ambient concentrations of aldehydes in relation to Beijing Olympic air pollution control measures

Science.gov (United States)

Gong, J. C.; Zhu, T.; Hu, M.; Zhang, L. W.; Cheng, H.; Zhang, L.; Tong, J.; Zhang, J.

2010-08-01

Aldehydes are ubiquitous constituents of the atmosphere. Their concentrations are elevated in polluted urban atmospheres. The present study was carried out to characterize three aldehydes of most health concern (formaldehyde, acetaldehyde, and acrolein) in a central Beijing site in the summer and early fall of 2008 (from June to October). Measurements were made before, during, and after the Beijing Olympics to examine whether the air pollution control measures implemented to improve Beijing's air quality during the Olympics had any impact on concentrations of the three aldehydes. Average concentrations of formaldehyde, acetaldehyde and acrolein were 29.34 ± 15.12 μg/m3, 27.09 ± 15.74 μg/m3 and 2.32 ± 0.95 μg/m3, respectively, for the entire period of measurements, all being the highest among the levels measured in cities around the world in photochemical smog seasons. Among the three measured aldehydes, only acetaldehyde had a substantially reduced mean concentration during the Olympic air pollution control period compared to the pre-Olympic period. Formaldehyde and acrolein followed the changing pattern of temperature and were each significantly correlated with ozone (a secondary product of photochemical reactions). In contrast, acetaldehyde was significantly correlated with several pollutants emitted mainly from local emission sources (e.g., NO2, CO, and PM2.5). These findings suggest that local direct emissions had a larger impact on acetaldehyde than formaldehyde and acrolein.

Results of concentration measurements of artificial radioactive aerosols in the lower atmosphere; Resultats des mesures de concentration, dans la basse atmosphere, des aerosols radioactifs artificiels

Energy Technology Data Exchange (ETDEWEB)

Ardouin, B; Jehanno, C; Labeyrie, J; Lambert, G; Tanaevsky, O; Vassy, E [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

1963-07-01

This report gives the results of the measurements of artificial gross-{beta}-radioactivity in aerosols in the lower atmosphere; these measurements have been made by the Electronic Physics Service of the Electronic Department, and by the Atmospheric Physics Laboratory of the Paris Science Faculty. The measurements were begun in September 1956 and were continued in an increasing number of stations both in France and in the rest of the world. The present report deals with the period up to the end of august 1961, that is up to the end of the nuclear moratorium. After recalling the constitution and the properties of radioactive aerosols present in the atmosphere, the authors describe the measurement methods, estimate their accuracy and discuss various aspects of the results. (authors) [French] Ce rapport contient les resultats des mesures de radioactivite {beta} globale d'origine artificielle des aerosols dans la basse atmosphere, effectuees conjointement par le Service d'Electronique Physique du Departement d'Electronique et le Laboratoire de Physique de l'Atmosphere de la Faculte des Sciences de Paris. Les mesures ont commence en septembre 1956 et ont ete poursuivies dans un nombre croissant de stations, tant en France que dans le reste du monde. Le present rapport s'arrete a la fin aout 1961, c'est-a-dire au moment de la reprise des essais nucleaires. Apres avoir rappele la constitution et les proprietes des aerosols radioactifs presents dans l'atmosphere, les auteurs indiquent les methodes de mesure utilisees, evaluent leur precision et discutent les differents aspects des resultats de leurs mesures. (auteurs)

Inversion of Atmospheric Tracer Measurements, Localization of Sources

Science.gov (United States)

Issartel, J.-P.; Cabrit, B.; Hourdin, F.; Idelkadi, A.

When abnormal concentrations of a pollutant are observed in the atmosphere, the question of its origin arises immediately. The radioactivity from Tchernobyl was de- tected in Sweden before the accident was announced. This situation emphasizes the psychological, political and medical stakes of a rapid identification of sources. In tech- nical terms, most industrial sources can be modeled as a fixed point at ground level with undetermined duration. The classical method of identification involves the cal- culation of a backtrajectory departing from the detector with an upstream integration of the wind field. We were first involved in such questions as we evaluated the ef- ficiency of the international monitoring network planned in the frame of the Com- prehensive Test Ban Treaty. We propose a new approach of backtracking based upon the use of retroplumes associated to available measurements. Firstly the retroplume is related to inverse transport processes, describing quantitatively how the air in a sam- ple originates from regions that are all the more extended and diffuse as we go back far in the past. Secondly it clarifies the sensibility of the measurement with respect to all potential sources. It is therefore calculated by adjoint equations including of course diffusive processes. Thirdly, the statistical interpretation, valid as far as sin- gle particles are concerned, should not be used to investigate the position and date of a macroscopic source. In that case, the retroplume rather induces a straightforward constraint between the intensity of the source and its position. When more than one measurements are available, including zero valued measurements, the source satisfies the same number of linear relations tightly related to the retroplumes. This system of linear relations can be handled through the simplex algorithm in order to make the above intensity-position correlation more restrictive. This method enables to manage in a quantitative manner the

Combining in situ and laboratory measurements of soil-atmosphere carbonyl sulfide fluxes from four different biomes across Europe

Science.gov (United States)

Kitz, Florian; Gomez-Brandon, Maria; Hammerle, Albin; Spielmann, Felix M.; Insam, Heribert; Ibrom, Andreas; Migliavacca, Mirco; Moreno, Gerardo; Noe, Steffen M.; Wohlfahrt, Georg

2017-04-01

Flux partitioning, the quantification of photosynthesis and respiration, is a major uncertainty in modelling the carbon cycle and in times when robust models are needed to assess future global changes a persistent problem. A promising new approach is to derive gross primary production (GPP) from measurements of the carbonyl sulfide (COS) flux, the most abundant sulfur-containing trace gas in the atmosphere, with a mean concentration of about 500 pptv in the troposphere. This is possible because COS and CO2 enter the leaf via a similar pathway and are processed by the same enzyme (carbonic anhydrase). A prerequisite for using COS as a proxy for photosynthesis is a robust estimation of all non-leaf sources and sinks in an ecosystem. Past studies described soils either as a sink or source, depending on their properties like soil temperature and soil water content. In 2016 we conducted field campaigns in Austria (managed temperate mountain grassland), Spain (savannah), Denmark (temperate beech forest) and Estonia (hemiboreal forest) to estimate the soil-atmosphere COS fluxes under ambient conditions in different biomes. We used self-built fused silica soil chambers to avoid COS emissions from built-in materials and to assess the impact of radiation. At the grassland sites (Austria, Spain) vegetation was removed below the chambers, therefor more radiation reached the soil surface compared to natural conditions. The grassland sites were characterized by highly positive COS fluxes during daytime and COS fluxes around zero during nighttime. In contrast, the soils at the forest sites (Denmark, Estonia), characterized by less radiation on the soil surface, acted as a sink for COS. The impact of other abiotic factors, like soil water content and soil temperature, varied between the ecosystems. In addition to the field measurements soil and litter samples were taken at the study sites and used to measure COS fluxes under controlled conditions in the lab. Results from the

Influence of a gaseous atmosphere on fatigue crack propagation

International Nuclear Information System (INIS)

Henaff, G.

2002-01-01

The paper presents a review of the current knowledge on the influence of gaseous atmospheres, and primarily ambient air, on fatigue crack propagation in metallic alloys. Experimental evidence of the effect of exposure to ambient air or any moist environment on fatigue crack propagation in steels is first proposed. The different interacting processes are analyzed so as to clearly uncouple the influence of the various factors on crack growth resistance. Two distinct mechanisms are identified: the adsorption of vapour molecules and hydrogen assisted fracture at crack tip. (author)

Folded tubular photometer for atmospheric measurements of NO2 and NO

Directory of Open Access Journals (Sweden)

J. W. Birks

2018-05-01

Full Text Available We describe and characterize a modular folded tubular photometer for making direct measurements of the concentrations of nitrogen dioxide (NO2 and specify how this method could be extended to measure other pollutants such as sulfur dioxide (SO2, ozone (O3, and black carbon particulate matter. Direct absorbance measurements using this photometer can be made across the spectral range from the ultraviolet (UV to the near infrared. The absorbance cell makes use of modular components (tubular detection cells and mirror cubes that allow construction of path lengths of up to 2 m or more while maintaining low cell volumes. The long path lengths and low cell volumes enable sensitive detection of ambient air pollutants down to low part-per-billion levels for gas species and aerosol extinctions down to 1 Mm−1, corresponding to  ∼  0.1 µg m−3 for black carbon particulates. Pressure equalization throughout the stages of the absorbance measurement is shown to be critical to accurate measurements of analyte concentrations. The present paper describes the application of this photometer to direct measurements of nitrogen dioxide (NO2 and the incorporation of design features that also enable measurement of nitric oxide (NO in the same instrument. Excellent agreement for ambient measurements along an urban roadside was found for both NO2 and NO measured by the folded tubular photometer compared to existing standard techniques. Compared to commonly used methods for measurements of NOx species, the advantages of this approach include (1 an absolute quantification for NO2 based on the Beer–Lambert law, thereby greatly reducing the frequency at which calibrations are required; (2 the direct measurement of NO2 concentration without prior conversion to NO as is required for the commonly used chemiluminescence method; (3 the use of modular components that allow construction of absorbance detection cells of varying lengths for extending the

Intercomparison of atmospheric water vapour measurements at a Canadian High Arctic site

Science.gov (United States)

Weaver, Dan; Strong, Kimberly; Schneider, Matthias; Rowe, Penny M.; Sioris, Chris; Walker, Kaley A.; Mariani, Zen; Uttal, Taneil; McElroy, C. Thomas; Vömel, Holger; Spassiani, Alessio; Drummond, James R.

2017-08-01

Water vapour is a critical component of the Earth system. Techniques to acquire and improve measurements of atmospheric water vapour and its isotopes are under active development. This work presents a detailed intercomparison of water vapour total column measurements taken between 2006 and 2014 at a Canadian High Arctic research site (Eureka, Nunavut). Instruments include radiosondes, sun photometers, a microwave radiometer, and emission and solar absorption Fourier transform infrared (FTIR) spectrometers. Close agreement is observed between all combination of datasets, with mean differences ≤ 1.0 kg m-2 and correlation coefficients ≥ 0.98. The one exception in the observed high correlation is the comparison between the microwave radiometer and a radiosonde product, which had a correlation coefficient of 0.92.A variety of biases affecting Eureka instruments are revealed and discussed. A subset of Eureka radiosonde measurements was processed by the Global Climate Observing System (GCOS) Reference Upper Air Network (GRUAN) for this study. Comparisons reveal a small dry bias in the standard radiosonde measurement water vapour total columns of approximately 4 %. A recently produced solar absorption FTIR spectrometer dataset resulting from the MUSICA (MUlti-platform remote Sensing of Isotopologues for investigating the Cycle of Atmospheric water) retrieval technique is shown to offer accurate measurements of water vapour total columns (e.g. average agreement within -5.2 % of GRUAN and -6.5 % of a co-located emission FTIR spectrometer). However, comparisons show a small wet bias of approximately 6 % at the high-latitude Eureka site. In addition, a new dataset derived from Atmospheric Emitted Radiance Interferometer (AERI) measurements is shown to provide accurate water vapour measurements (e.g. average agreement was within 4 % of GRUAN), which usefully enables measurements to be taken during day and night (especially valuable during polar night).

Atmospheric formaldehyde and acetaldehyde at the campus University of Hiroshima, Japan

Directory of Open Access Journals (Sweden)

Sonia Naomi Nomi

2010-09-01

Full Text Available Ambient levels of formaldehyde (HCHO and acetaldehyde (CH3CHO were measured at Hiroshima (Japan during spring and summer of 2005. Measurements of O3, NOx, and SO2 were simultaneously conducted, in an attempt to identify temporal profiles and sources for these aldehydes. Atmospheric aldehydes were collected using C18 silica gel cartridges coated with an acidic solution of 2, 4-dinitrophenylhydrazine (2,4-DNPH and analyzed by high performance liquid chromatography with UV/VIS detection adjusted to 360 nm. Summer concentrations were higher than spring levels. FA concentrations during spring period ranged from 0.50 to 1.05 ppb and AA concentrations ranged from 0.17 to 1.31 ppb; during summer their concentrations ranged from 1.55 to 4.12 ppb and 0. 34 to 2.03 ppb. Average FA/AA in spring and summer were 3.09 and 3.72 suggesting biogenic emissions of aldehydes. The levels of FA and AA, their temporal variations, and their concentration ratio (FA/AA indicated that photochemical reactions contributed significantly to the formation of atmospheric aldehydes at the study site.

Bio-organic materials in the atmosphere and snow: measurement and characterization.

Science.gov (United States)

Ariya, P A; Kos, G; Mortazavi, R; Hudson, E D; Kanthasamy, V; Eltouny, N; Sun, J; Wilde, C

2014-01-01

Bio-organic chemicals are ubiquitous in the Earth's atmosphere and at air-snow interfaces, as well as in aerosols and in clouds. It has been known for centuries that airborne biological matter plays various roles in the transmission of disease in humans and in ecosystems. The implication of chemical compounds of biological origins in cloud condensation and in ice nucleation processes has also been studied during the last few decades, and implications have been suggested in the reduction of visibility, in the influence on oxidative potential of the atmosphere and transformation of compounds in the atmosphere, in the formation of haze, change of snow-ice albedo, in agricultural processes, and bio-hazards and bio-terrorism. In this review we critically examine existing observation data on bio-organic compounds in the atmosphere and in snow. We also review both conventional and cutting-edge analytical techniques and methods for measurement and characterisation of bio-organic compounds and specifically for microbial communities, in the atmosphere and snow. We also explore the link between biological compounds and nucleation processes. Due to increased interest in decreasing emissions of carbon-containing compounds, we also briefly review (in an Appendix) methods and techniques that are currently deployed for bio-organic remediation.

The influence of ambient light on the driver

Science.gov (United States)

Klinger, Karsten D.; Lemmer, Uli

2008-04-01

Increasingly, cars are fitted with interior ambient lighting which is switched on while driving. This special kind of interior light emphasizes the interior design of the car, it makes a car look special and gives the buyers a new option to personalize their automobiles. But how does ambient interior light influence the driver? We conducted a series of over 50 tests to study the influence of interior ambient light on contrast perception under different illumination levels, colors and positions of the illuminated areas. Our tests show that in many cases the ambient lighting can improve the visual contrast for seeing objects in the headlamp beam. But the test persons mentioned that the tested brightness looked too bright and that they felt glared. The measured values instead proved that no disability glare exists. Therefore, provided that the drivers can adjust the intensity of the ambient light to avoid glare, the ambient light has no negative effect on the drivers' contrast perception.

Atmospheric aerosol in an urban area: Comparison of measurement instruments and methodologies and pulmonary deposition assessment

International Nuclear Information System (INIS)

Berico, M.; Luciani, A.; Formignani, M.

1996-07-01

In March 1995 a measurement campaign of atmospheric aerosol in the Bologna urban area (Italy) was carried out. A transportable laboratory, set up by ENEA (Italian national Agency for New Technologies, Energy and the Environment) Environmental Department (Bologna), was utilized with instruments for measurement of atmospheric aerosol and meteorological parameters. The aim of this campaign was of dual purpose: to characterize aerosol in urban area and to compare different instruments and methodologies of measurements. Mass concentrations measurements, evaluated on a 23-hour period with total filter, PM10 dichotomous sampler and low pressure impactor (LPI Berner), have provided information respectively about total suspended particles, respirable fraction and granulometric parameters of aerosol. Eight meteorologic parameters, number concentration of submicromic fraction of aerosol and mass concentration of micromic fraction have been continually measured. Then, in a daytime period, several number granulometries of atmospheric aerosol have also been estimated by means of diffusion battery system. Results related to different measurement methodologies and granulometric characteristics of aerosol are presented here. Pulmonary deposition of atmospheric aerosol is finally calculated, using granulometries provided by LPI Brener and ICRP 66 human respiratory tract model

High Precision Continuous and Real-Time Measurement of Atmospheric Oxygen Using Cavity Ring-Down Spectroscopy.

Science.gov (United States)

Kim-Hak, D.; Hoffnagle, J.; Rella, C.; Sun, M.

2016-12-01

Oxygen is a major and vital component of the Earth atmosphere representing about 21% of its composition. It is consumed or produced through biochemical processes such as combustion, respiration, and photosynthesis. Although atmospheric oxygen is not a greenhouse gas, it can be used as a top-down constraint on the carbon cycle. The variation observations of oxygen in the atmosphere are very small, in the order of the few ppm's. This presents the main technical challenge for measurement as a very high level of precision is required and only few methods including mass spectrometry, fuel cell, and paramagnetic are capable of overcoming it. Here we present new developments of a high-precision gas analyzer that utilizes the technique of Cavity Ring-Down Spectroscopy to measure oxygen concentration and oxygen isotope. Its compact and ruggedness design combined with high precision and long-term stability allows the user to deploy the instrument in the field for continuous monitoring of atmospheric oxygen level. Measurements have a 1-σ 5-minute averaging precision of 1-2 ppm for O2 over a dynamic range of 0-20%. We will present supplemental data acquired from our 10m tower measurements in Santa Clara, CA.

Armazenamento de dois tipos de sapoti sob condição de ambiente Storage of two types of sapodilla under ambient condition

Directory of Open Access Journals (Sweden)

Maria Raquel Alcântara de Miranda

2002-12-01

Full Text Available Esse trabalho objetiva avaliar a vida útil de dois tipos de sapoti em temperatura ambiente, com ou sem atmosfera modificada (filme de PVC. O experimento constituiu-se no armazenamento dos frutos, coletados na estação experimental da Embrapa em Paraipaba-CE, em temperatura ambiente (24 ± 2ºC e 90 ± 5% U.R. e dispostos em bandejas com ou sem filme de PVC. Dois tipos de sapoti foram avaliados quanto à perda de peso, textura, sólidos solúveis totais, açúcares redutores e totais, acidez total titulável e amido. Os frutos sob atmosfera modificada apresentaram uma menor perda de peso, mas apresentaram uma redução mais rápida na firmeza da polpa. Os dois tipos de sapoti apresentaram um decréscimo no teor de sólidos solúveis, acidez, açúcares solúveis totais e pH e um aumento em açúcares redutores ao longo do armazenamento, independentemente das diferentes atmosferas de conservação. Os resultados indicam que os frutos do tipo II (formato da sapota possuem uma maior vida útil pós-colheita.This work aims to evaluate the postharvest life of two types of sapodilla at ambient temperature and with or without modified atmosphere (PVC film packing. The experiment consisted in storing fruits, harvested at Embrapa´s (Agroindústria Tropical Experimental Station located in Paraipaba, Ceará, Brazil, under ambient condition (24 ± 2ºC and 90 ± 5% U.R, on retail trays where half of these trays was wrapped in PVC and the other half, was not wrapped. Fruits of two types were evaluated for weight loss; pulp firmness; total soluble solids; titrable acidity; pH; total soluble sugars, reducing sugars and starch contents. Fruits stored under MA had less weight loss and greater reduction in pulp firmness when compared to those under AA. Decreases in acidity, soluble solids and total sugar contents and pH were found in both types of fruit during storage under both atmosphere conditions, as well as an increase in reduced sugars content. The type

Detecting charging state of ultra-fine particles: instrumental development and ambient measurements

Directory of Open Access Journals (Sweden)

L. Laakso

2007-01-01

Full Text Available The importance of ion-induced nucleation in the lower atmosphere has been discussed for a long time. In this article we describe a new instrumental setup – Ion-DMPS – which can be used to detect contribution of ion-induced nucleation on atmospheric new particle formation events. The device measures positively and negatively charged particles with and without a bipolar charger. The ratio between "charger off" to "charger on" describes the charging state of aerosol particle population with respect to equilibrium. Values above one represent more charges than in an equilibrium (overcharged state, and values below unity stand for undercharged situation, when there is less charges in the particles than in the equilibrium. We performed several laboratory experiments to test the operation of the instrument. After the laboratory tests, we used the device to observe particle size distributions during atmospheric new particle formation in a boreal forest. We found that some of the events were clearly dominated by neutral nucleation but in some cases also ion-induced nucleation contributed to the new particle formation. We also found that negative and positive ions (charged particles behaved in a different manner, days with negative overcharging were more frequent than days with positive overcharging.

Ambient air quality of karachi city as reflected by atmospheric particulate matter (PM/sub 10/) concentrations

International Nuclear Information System (INIS)

Hashmi, D.R.; Shareef, A.

2016-01-01

The present study examines the variation of ambient aerosol (PM/sub 10/) concentrations in Karachi, city. Samples were collected from ten different locations, representative of urban background, residential, traffic and industrial areas from 2007 to 2011. At each location, PM/sub 10/) was measured continuously from 08:00 am to 06:00 pm at local time. The maximum 10 h average particulate matter (PM/sub 10/) mass concentrations were found at Tibet Centre (440.1 mg/m/sup 3/) and minimum at PCSIR Campus (21.7 mg/m/sup 3/) during 2008. A rising trend during 2008 may be due to the civil works for bridges and extension of roads at different locations in Karachi. The results also suggest that urban traffic and industrial areas appeared to have higher PM/sub 10/) concentration than residential and background areas. (author)

Determinação de Ácidos Carboxílicos na Atmosfera Urbana de São Paulo: uma abordagem analítica e ambiental Carboxylic acids measuremsnts in urban air of são paulo city: an analytical and environmental approach

Directory of Open Access Journals (Sweden)

Silvia R. Souza

1997-06-01

Full Text Available In this work, analytical strategies are evaluated in order to measure accurately the ambient levels of atmospheric organic acids. Environmental considerations about the determination of low molecular weight mono- and di-carboxylic acids from urban areas of São Paulo are described.

Atmospheric ventilation corridors and coefficients for pollution plume ...

African Journals Online (AJOL)

This study presents a comparative investigation of atmospheric ventilation corridors and coefficients for gaseous pollution plume released from an isolated industrial facility into the ambient air of the host community in Ile-Ife suburb, southwest Nigeria. For the months of September to December in the year 2012 and 2013, ...

iSPEX: everybody can measure atmospheric aerosols with a smartphone spectropolarimeter

Science.gov (United States)

Snik, F.; Heikamp, S.; de Boer, J.; Keller, C. U.; van Harten, G.; Smit, J. M.; Rietjens, J. H. H.; Hasekamp, O.; Stam, D. M.; Volten, H.; iSPEX Team

2012-04-01

An increasing amount people carry a mobile phone with internet connection, camera and large computing power. iSPEX, a spectropolarimetric add-on with complementary app, instantly turns a smartphone into a scientific instrument to measure dust and other aerosols in our atmosphere. A measurement involves scanning the blue sky, which yields the angular behavior of the degree of linear polarization as a function of wavelength, which can unambiguously be interpreted in terms of size, shape and chemical composition of the aerosols in the sky directly above. The measurements are tagged with location and pointing information, and submitted to a central database where they will be interpreted and compiled into an aerosol map. Through crowdsourcing, many people will thus be able to contribute to a better assessment of health risks of particulate matter and of whether or not volcanic ash clouds are dangerous for air traffic. It can also contribute to the understanding of the relationship between atmospheric aerosols and climate change. We will give a live presentation of the first iSPEX prototype. Furthermore, we will present the design and the plans for producing the iSPEX add-on, app and website. We aim to distribute thousands of iSPEX units, such that a unique network of aerosol measurement equipment is created. Many people will thus contribute to the solution of several urgent social and scientific problems, and learn about the nature of light, remote sensing and the issues regarding atmospheric aerosols in the process. In particular we focus on school classes where smartphones are usually considered a nuisance, whereas now they can be a crucial part of various educational programs in science class.

Five-year measurements of ambient ammonia and its relationships with other trace gases at an urban site of Delhi, India

Science.gov (United States)

Saraswati; Sharma, S. K.; Mandal, T. K.

2018-04-01

In this study, we present the 5-year measurements of ambient ammonia (NH3), oxides of nitrogen (NO and NO2) and carbon monoxide (CO) along with the meteorological parameters at an urban site of Delhi, India from January 2011 to December 2015. The average mixing ratios of ambient NH3, NO, NO2 and CO over the entire period of observations were recorded as 19.3 ± 4.4 (ppb), 20.1 ± 5.9 (ppb), 18.6 ± 4.6 (ppb) and 1.8 ± 0.5 (ppm), respectively. The mixing ratios of NH3, NO, NO2 and CO were recorded highest during winter season, followed by summer and monsoon season. In the present case, a substantial seasonal variation of NH3 was observed during all the seasons except NO, NO2 and CO. The results emphasized that the traffic could be one of the significant sources of ambient NH3 at the urban site of Delhi as illustrated by positive correlations of NH3 with traffic related pollutants (NO x and CO). Surface wind as well as back trajectory analysis also supports the road side traffic and agricultural activities at the nearby area indicating possible major sources of ambient NH3 at observational site. Trajectory analysis, potential source contribution function and concentration weighted trajectory analysis indicated the surrounding nearby areas (NCR, Haryana, Punjab, Rajasthan and Uttar Pradesh) as a significant source region of ambient NH3 at the observational site of Delhi.

Discovery and measurement of an isotopically distinct source of sulfate in Earth's atmosphere.

Science.gov (United States)

Dominguez, Gerardo; Jackson, Terri; Brothers, Lauren; Barnett, Burton; Nguyen, Bryan; Thiemens, Mark H

2008-09-02

Sulfate (SO(4)) and its precursors are significant components of the atmosphere, with both natural and anthropogenic sources. Recently, our triple-isotope ((16)O, (17)O, (18)O) measurements of atmospheric sulfate have provided specific insights into the oxidation pathways leading to sulfate, with important implications for models of the sulfur cycle and global climate change. Using similar isotopic measurements of aerosol sulfate in a polluted marine boundary layer (MBL) and primary sulfate (p-SO(4)) sampled directly from a ship stack, we quantify the amount of p-SO(4) found in the atmosphere from ships. We find that ships contribute between 10% and 44% of the non-sea-salt sulfate found in fine [diameter (D) sea salt particles may lead to the rapid removal of SO(2) in the MBL. When combined with the longer residence time of p-SO(4) emissions in the MBL, these findings suggest that the importance of p-SO(4) emissions in marine environments may be underappreciated in global chemical models. Given the expected increase of international shipping in the years to come, these findings have clear implications for public health, air quality, international maritime law, and atmospheric chemistry.

Atmospheric effects on the photovoltaic performance of hybrid perovskite solar cells

KAUST Repository

Sheikh, Arif D.

2015-06-01

Organometal trihalide perovskite solar cells have recently attracted lots of attention in the photovoltaic community due to their escalating efficiency and solution processability. The most efficient organometallic mixed-halide sensitized solar cells often employ 2,2′7,7′-tetrakis-(N,N-di-p-methoxyphenyl-amine)-9,9′-spirobifluorene (spiro-MeOTAD) as the hole-transporting material. In this work, we investigated the effect of different atmospheric storage conditions, particularly vacuum, dry nitrogen, and dry air, on the photovoltaic performance of TiO2-CH3NH3PbI3-xClx-spiro-MeOTAD solar cells. We found that spin coating of spiro-MeOTAD in an oxygen atmosphere alone was not adequate to functionalize its hole-transport property completely, and our systematic experiments revealed that the device efficiency depends on the ambient atmospheric conditions during the drying process of spiro-MeOTAD. Complementary incident photon to current conversion efficiency (IPCE), light absorption and photoluminescence quenching measurements allowed us to attribute the atmosphere-dependent efficiency to the improved electronic characteristics of the solar cells. Furthermore, our Fourier transform infrared and electrical impedance measurements unambiguously detected modifications in the spiro-MeOTAD after the drying processes in different gas environments. Our findings demonstrate that proper oxidization and p-doping in functionalizing spiro-MeOTAD play a very critical role in determining device performance. These findings will facilitate the search for alternative hole-transporting materials in high-performance perovskite solar cells with long-term stability.

Improved radon-flux-measurement system for uranium-tailings pile measurement

International Nuclear Information System (INIS)

Freeman, H.D.

1981-10-01

The Pacific Northwest Laboratory (PNL) is developing cover technology for uranium mill tailings that will inhibit the diffusion of radon to the atmosphere. As part of this cover program, an improved radon flux measurement system has been developed. The radon measurement system is a recirculating, pressure-balanced, flow-through system that uses activated carbon at ambient temperatures to collect the radon. With the system, an area of 0.93 m 2 is sampled for periods ranging from 1 to 12 h. The activated carbon is removed from the radon trap and the collected radon is determined by counting the 214 Bi daughter product. Development of the system included studies to determine the efficiency of activated carbon, relative calibration measurements and field measurements made during 1980 at the inactive tailings pile in Grand Junction, Colorado. Results of these studies are presented

Periodismo ambiental

Directory of Open Access Journals (Sweden)

Lucía Lemos

2015-01-01

Full Text Available Los periodistas toman el tema del medio ambiente cada vez más en serio. El uso de temas relacionados con el medio ambiente, debe estar ligado al análisis socio-económico y a las posibilidades de comunicación y educación de diferentes regiones del mundo. A continuación se presenta un resumen de la situación ambiental, las acciones de prensa y comunicación que se llevan a cabo en América Central (Panamá, El Salvador, Costa Rica y en Sudamérica Brasil,Colombia, Chile, México, y Perú. Se concluye en la necesidad de formar hábitos ecológicos. Los comunicadores deben presentar soluciones a los problemas, fomentar campañas comunes, compartir información y velar por el ambiente ambiente para que las generaciones futuras no tengan que perecer.

Monitoring method for an ambient Gamma exposure rate and its measurement analysis

Energy Technology Data Exchange (ETDEWEB)

Lee, Mo Sung [Cheongju Univ., Cheongju (Korea, Republic of); Woo, Jong Kwan [University of Seoul, Seoul (Korea, Republic of)

2006-12-15

Daily and seasonal variations of the ambient gamma ray exposure rates were measured by using a pressurized ion chamber from January 2003 to December 2005 in the Cheongju Regional Radiation Monitoring Post and the patterns of the distributions were studied. The annual average of the daily variation of the exposure rate was {approx}0.17 {mu}R/h. The exposure rate was found to be maximum during 8:00 am to 9:00 am and minimum during 8:00 pm to 10:00 pm. For the annual data, the exposure rate was the minimum during the month of February. The exposure rate increased from February to mid-October (except during the period from May to July with no change) and decreased from October to February. The seasonal variation was found to be about 1 {mu}R/h. Most of the measured values (96%) of the exposure rates fell under the normal distribution with a deviation of less than 4.8% and the remaining 4% had large fluctuations caused mainly by the rainfalls.

Annual report of the ambient air quality measurements in Austria 2000

International Nuclear Information System (INIS)

Spangl, W.; Schneider, J.

2001-01-01

This report presents the result of the ambient air quality measurements conducted according to the air quality act (Austrian Federal Law Gazette I 115/97) in Austria in 2000. This act defines ambient air quality limit values for sulphur dioxide, nitrogen dioxide, total suspended particulates (TSP), carbon monoxide, benzene, lead in air, deposition (total mass including lead and cadmium) and a target value for ozone. The report also comprises results of explorative measurements of PM10 and PM2,5. Only one exceedance of the limit value for sulphur dioxide (0,20 mg/m 3 as half hour mean value, not to be exceeded more than three times a day; 0,50 mg/m 3 as half hour mean value) was observed. The exceedance was caused by air pollution transport from Slovenia. The limit values for nitrogen dioxide and total suspended particulates were exceeded quite frequently in 2000. For nitrogen dioxide, mainly traffic stations were affected. Exceedances of the limit value (0,20 mg/m 3 as half hour mean value) were observed both during winter episodes with unfavourable conditions for dispersion, as well as in spring/summer at a heavily frequented road during episodes with high ozone levels, causing rapid oxidation of NO to NO 2 . Exceedances of the limit value for total suspended particulates (0,15 mg/m 3 as daily mean value) were predominately recorded in urban areas in the vicinity of heavily frequented streets, especially in southern alpine basins and valleys with unfavourable dispersion conditions. The highest pollution was recorded at a heavily frequented crossroad in Graz. For carbon monoxide (eight hour mean value of 10 mg/m 3 ), benzene ( 10 μg/m 3 as annual mean value) and lead (1 μg/m 3 , as annual mean value), no exceedances were recorded. The pollution levels of sulphur dioxide and carbon monoxide show a strong decrease during the last decade, whereas for nitrogen dioxide and particulate matter no clear trend can be identified. The target value of ozone is exceeded at

Modeling of atmospheric pollutant transfers

International Nuclear Information System (INIS)

Jourdain, F.

2007-01-01

Modeling is today a common tool for the evaluation of the environmental impact of atmospheric pollution events, for the design of air monitoring networks or for the calculation of pollutant concentrations in the ambient air. It is even necessary for the a priori evaluation of the consequences of a pollution plume. A large choice of atmospheric transfer codes exist but no ideal tool is available which allows to model all kinds of situations. The present day approach consists in combining different types of modeling according to the requested results and simulations. The CEA has a solid experience in this domain and has developed independent tools for the impact and safety studies relative to industrial facilities and to the management of crisis situations. (J.S.)

Design of a fiber optical sensor for atmospheric electric field measurement

International Nuclear Information System (INIS)

Baghdasaryan, H.V.; Knyazyan, T.M.; Daryan, A.V.

2016-01-01

All-optical sensor for atmospheric electric field detection and measurement is suggested and numerically modelled. Thin electro- optical crystal sandwiched between two distributed Bragg reflectors (DBRs) forming multilayer Gires-Tournois (G-T) microresonator is used as a sensitive part of the electric field sensor. In the sensor device, an optical fiber delivers the wideband light spectrum to the sensing multilayer structure of G-T microresonator. The reflectance spectrum of the sensor contains information on the electric field strength and direction. The relevant reflectance peaks’ shift in the reflected spectrum can be observed by an optical spectrum analyzer (OSA). Numerical modelling has been done by the method of single expression that is a suitable tool for multi-boundary problems solution. The obtained results of modelling will be useful in a new type of non-distorting sensor’s elaboration for atmospheric electric field detection and measurement. (author)

Comparison of ambient aerosol extinction coefficients obtained from in-situ, MAX-DOAS and LIDAR measurements at Cabauw

Directory of Open Access Journals (Sweden)

P. Zieger

2011-03-01

Full Text Available In the field, aerosol in-situ measurements are often performed under dry conditions (relative humidity RH<30–40%. Since ambient aerosol particles experience hygroscopic growth at enhanced RH, their microphysical and optical properties – especially the aerosol light scattering – are also strongly dependent on RH. The knowledge of this RH effect is of crucial importance for climate forcing calculations or for the comparison of remote sensing with in-situ measurements. Here, we will present results from a four-month campaign which took place in summer 2009 in Cabauw, The Netherlands. The aerosol scattering coefficient σ_sp(λ was measured dry and at various, predefined RH conditions between 20 and 95% with a humidified nephelometer. The scattering enhancement factor f(RH,λ is the key parameter to describe the effect of RH on σ_sp(λ and is defined as σ_sp(RH,λ measured at a certain RH divided by the dry σ_sp(dry,λ. The measurement of f(RH,λ together with the dry absorption measurement (assumed not to change with RH allows the determination of the actual extinction coefficient σ_ep(RH,λ at ambient RH. In addition, a wide range of other aerosol properties were measured in parallel. The measurements were used to characterize the effects of RH on the aerosol optical properties. A closure study showed the consistency of the aerosol in-situ measurements. Due to the large variability of air mass origin (and thus aerosol composition a simple parameterization of f(RH,λ could not be established. If f(RH,λ needs to be predicted, the chemical composition and size distribution need to be known. Measurements of four MAX-DOAS (multi-axis differential optical absorption spectroscopy instruments were used to retrieve vertical profiles of σ_ep(λ. The values of the lowest layer were compared to the in-situ values after conversion of the latter ones to ambient

Effect of corrosive marine atmosphere on construction materials in Tanzania: Exposure sites and preliminary results

International Nuclear Information System (INIS)

Mmari, A.G.; Uiso, C.B.S.; Makundi, I.N.; Potgieter-Vermaak, S.S.; Potgieter, J.H.; Van Grieken, R.

2007-01-01

Air pollution studies in Africa are limited and the influence of ambient air quality on buildings and constructions have not been investigated in the larger part of Sub-Saharan Africa. The increasing burden of emission from industry, traffic and coal power plants on ambient air pollution in Sub-Saharan Africa necessitated reviewing previous and current studies. In South Africa a 20-year exposure program, focusing on the effect of ambient exposure on various metals and alloys, showed that the amount of rainfall, relative humidity, atmospheric pollution, wind speed, solar radiation and structural design are some of the factors controlling atmospheric corrosion. Tanzania, being among the Sub-Saharan African countries and partly bordered by Indian ocean, the main source of marine atmosphere, experiences corrosive degradation on metal roofing and cementitious materials. This paper describes the exposure site set-up and will report on some preliminary results of air quality and its relation with the meteorological conditions, as well as surface changes observed, for the year one of exposure. These will thereafter be compared to the completed European and Asian studies, as reported by CLRTAP and RAPIDC respectively. (author)

Development of a Wind Plant Large-Eddy Simulation with Measurement-Driven Atmospheric Inflow

Energy Technology Data Exchange (ETDEWEB)

Quon, Eliot W.; Churchfield, Matthew J.; Cheung, Lawrence; Kern, Stefan

2017-01-09

This paper details the development of an aeroelastic wind plant model with large-eddy simulation (LES). The chosen LES solver is the Simulator for Wind Farm Applications (SOWFA) based on the OpenFOAM framework, coupled to NREL's comprehensive aeroelastic analysis tool, FAST. An atmospheric boundary layer (ABL) precursor simulation was constructed based on assessments of meteorological tower, lidar, and radar data over a 3-hour window. This precursor was tuned to the specific atmospheric conditions that occurred both prior to and during the measurement campaign, enabling capture of a night-to-day transition in the turbulent ABL. In the absence of height-varying temperature measurements, spatially averaged radar data were sufficient to characterize the atmospheric stability of the wind plant in terms of the shear profile, and near-ground temperature sensors provided a reasonable estimate of the ground heating rate describing the morning transition. A full aeroelastic simulation was then performed for a subset of turbines within the wind plant, driven by the precursor. Analysis of two turbines within the array, one directly waked by the other, demonstrated good agreement with measured time-averaged loads.

Evidence of feasible hardness test on Mars using ratio of ionic/neutral emission intensities measured with laser-induced breakdown spectroscopy in low pressure CO_2 ambient gas

International Nuclear Information System (INIS)

Abdulmadjid, Syahrun Nur; Lahna, Kurnia; Idris, Nasrullah; Pardede, Marincan; Suyanto, Hery; Ramli, Muliadi; Marpaung, Alion Mangasi; Hedwig, Rinda; Lie, Zener Sukra; Kurniawan, Davy Putra; Kurniawan, Koo Hendrik; Lie, Tjung Jie; Tjia, May On; Kagawa, Kiichiro

2016-01-01

An experimental study is conducted on the possibility and viability of performing hardness measurement of the various stone and chert samples in low pressure (600 Pa) CO_2 ambient gas, a condition that is encountered in the Mars atmosphere. For this study, a nanosecond Nd-YAG laser is employed to generate plasma emission from the samples with different degrees of hardness. This technique is developed in light of the role of the shock wave in the generation of a laser-induced plasma. It was previously shown that the speed of the shock front depends on the hardness of the sample, and a positive relationship was found between the speed of the shock front and the ionization rate of the ablated atoms. Hence, the ratio of the intensity between the Mg II 279.5 nm and Mg I 285.2 nm emission lines detected from the laser-induced plasma can be used to estimate the hardness of a material. In fact, it is shown that the ratio changes linearly with respect to changes of sample hardness. The result has thus demonstrated the feasibility and viability of using LIBS for non contact hardness measurement on Mars.

Skin perfusion measurement: the normal range, the effects of ambient temperature and its clinical application

International Nuclear Information System (INIS)

Henry, R.E.; Malone, J.M.; Daly, M.J.; Hughes, J.H.; Moore, W.S.

1982-01-01

Quantitation of skin perfusion provides objective criteria to determine the optimal amputation level in ischemic limb disease, to assess the maturation of pedicle flaps in reconstructive surgery, and to select appropriate treatment for chronic skin ulcers. A technique for measurement of skin perfusion using intradermal (ID) Xe-133 and a gamma camera/minicomputer system was previously reported. An update of this procedure is now reported, the normal range for the lower extremity in men, observations on the effects of ambient temperature, and an experience using the procedure to determine amputation level

Humidity Effects on Fragmentation in Plasma-Based Ambient Ionization Sources.

Science.gov (United States)

Newsome, G Asher; Ackerman, Luke K; Johnson, Kevin J

2016-01-01

Post-plasma ambient desorption/ionization (ADI) sources are fundamentally dependent on surrounding water vapor to produce protonated analyte ions. There are two reports of humidity effects on ADI spectra. However, it is unclear whether humidity will affect all ADI sources and analytes, and by what mechanism humidity affects spectra. Flowing atmospheric pressure afterglow (FAPA) ionization and direct analysis in real time (DART) mass spectra of various surface-deposited and gas-phase analytes were acquired at ambient temperature and pressure across a range of observed humidity values. A controlled humidity enclosure around the ion source and mass spectrometer inlet was used to create programmed humidity and temperatures. The relative abundance and fragmentation of molecular adduct ions for several compounds consistently varied with changing ambient humidity and also were controlled with the humidity enclosure. For several compounds, increasing humidity decreased protonated molecule and other molecular adduct ion fragmentation in both FAPA and DART spectra. For others, humidity increased fragment ion ratios. The effects of humidity on molecular adduct ion fragmentation were caused by changes in the relative abundances of different reagent protonated water clusters and, thus, a change in the average difference in proton affinity between an analyte and the population of water clusters. Control of humidity in ambient post-plasma ion sources is needed to create spectral stability and reproducibility.

Plume Splitting in a Two-layer Stratified Ambient Fluid

Science.gov (United States)

Ma, Yongxing; Flynn, Morris; Sutherland, Bruce