J. B. Nowak

Unexpected high levels of NO observed at South Pole

Reported here are the first Austral summer measurements of NO at South Pole (SP). They arc unique in that the levels are one to two orders of magnitude higher (i.e., median, 225 pptv) than measured at other polar sites. The available evidence suggests that these elevated levels arc the result of photodenitrification of the snowpack, in conjunction with a very thin atmospheric mixing depth. Important chemical consequences included finding the atmospheric oxidizing power at SP to be an order of magnitude higher than expected.

Infrared spectroscopy of model tropospheric aerosols as a function of relative humidity: Observation of deliquescence and crystallization

The infrared extinction spectra of model tropospheric aerosols, (NH4)2SO4, NH4HSO4, NaCl, and artificial seawater, have been measured as a function of relative humidity. Experimentally, submicron-sized aerosol particles are spectroscopically monitored as they flow at atmospheric pressure on a 30-s timescale through a room temperature infrared absorption cell. By monitoring absorption features due to either constituent ions or water molecules, we infer both the physical phase and, to some degree, the chemical composition of the aerosol particles. It is observed that (1) solid (NH4) SO4 and NaCl aerosol particles exhibit deliquescence at 79±1% and 75±1% relative humidity, respectively, very close to their thermodynamic values; (2) (NH4)2SO4 and NaCl liquid particles exhibit crystallization at relative humidities of 33±2% and 43±2%, respectively, well below their deliquescence points; (3) NH4HSO4 aqueous aerosol particles remain in the liquid state to relative humidities as low as 2%, far below the thermodynamic deliquescence humidity of 39%; and (4) artificial seawater aerosol particles show strong H2O absorption features at low relative humidities, arising either because the particle has not crystallized or because solid hydrates of Mg2+ salts have formed. These observations illustrate the extent to which water will be present in the aerosol condensed phase in both laboratory experiments and in the atmosphere. Specifically, for (NH4)2SO4 and NaCl particles, the water content is expected to be low at relative humidities below the crystallization point, whereas the aerosol particles will be liquid at higher relative humidities. NH4HSO4 and artificial seawater aerosols will both contain significant quantities of water down to very low relative humidities, present either as a liquid or possibly as hydrates of Mg2+ in the case of artificial seawater. By adding gas-phase D2O to NH4HSO4 and artificial seawater aerosols at low relative humidity, condensed phase D2O features appear in the spectra, indicating facile exchange of water between the gas-phase and the particles. Conversely, aerosols with low water content, such as solid NaCl, do not exhibit condensed-phase D2O features in the presence of gas-phase D2O.

Quantifying atmospheric methane emissions from the Haynesville, Fayetteville, and northeastern Marcellus shale gas production regions

We present measurements of methane (CH4) taken aboard a NOAA WP-3D research aircraft in 2013 over the Haynesville shale region in eastern Texas/northwestern Louisiana, the Fayetteville shale region in Arkansas, and the northeastern Pennsylvania portion of the Marcellus shale region, which accounted for the majority of Marcellus shale gas production that year. We calculate emission rates from the horizontal CH4 flux in the planetary boundary layer downwind of each region after subtracting the CH4 flux entering the region upwind. We find 1 day CH4 emissions of (8.0 ± 2.7) × 107 g/h from the Haynesville region, (3.9 ± 1.8) × 107 g/h from the Fayetteville region, and (1.5 ± 0.6) × 107 g/h from the Marcellus region in northeastern Pennsylvania. Finally, we compare the CH4 emissions to the total volume of natural gas extracted from each region to derive a loss rate from production operations of 1.0–2.1% from the Haynesville region, 1.0–2.8% from the Fayetteville region, and 0.18–0.41% from the Marcellus region in northeastern Pennsylvania. The climate impact of CH4 loss from shale gas production depends upon the total leakage from all production regions. The regions investigated in this work represented over half of the U.S. shale gas production in 2013, and we find generally lower loss rates than those reported in earlier studies of regions that made smaller contributions to total production. Hence, the national average CH4 loss rate from shale gas production may be lower than values extrapolated from the earlier studies.

Measurements of OH, H2SO4, and MSA at the South Pole during ISCAT

The first measurements of OH, H2SO4, and MSA performed at the South Pole as part of the Investigation of Sulfur Chemistry in the Antarctic Troposphere (ISCAT) study are presented. OH concentrations were found to be quite elevated for such a dry environment, with average values of 2x106 molecule cm−3. Model simulations suggest that much of the observed OH is a result of unexpectedly high NO concentrations. Concentrations of H2SO4 and MSA were generally low with average values of 2.5x105 and 1x105 molecule cm−3, respectively. Major variations in the concentration levels of the above species were found to have a high correlation with changes in the polar mixing layer as estimated from the measured temperature difference from 22 to 2m above the snow surface. Chemical details are discussed.

Formation of Low Volatility Organic Compounds and Secondary Organic Aerosol from Isoprene Hydroxyhydroperoxide Low-NO Oxidation.

Gas-phase low volatility organic compounds (LVOC), produced from oxidation of isoprene 4-hydroxy-3-hydroperoxide (4,3-ISOPOOH) under low-NO conditions, were observed during the FIXCIT chamber study. Decreases in LVOC directly correspond to appearance and growth in secondary organic aerosol (SOA) of consistent elemental composition, indicating that LVOC condense (at OA below 1 μg m(-3)). This represents the first simultaneous measurement of condensing low volatility species from isoprene oxidation in both the gas and particle phases. The SOA formation in this study is separate from previously described isoprene epoxydiol (IEPOX) uptake. Assigning all condensing LVOC signals to 4,3-ISOPOOH oxidation in the chamber study implies a wall-loss corrected non-IEPOX SOA mass yield of ∼4%. By contrast to monoterpene oxidation, in which extremely low volatility VOC (ELVOC) constitute the organic aerosol, in the isoprene system LVOC with saturation concentrations from 10(-2) to 10 μg m(-3) are the main constituents. These LVOC may be important for the growth of nanoparticles in environments with low OA concentrations. LVOC observed in the chamber were also observed in the atmosphere during SOAS-2013 in the Southeastern United States, with the expected diurnal cycle. This previously uncharacterized aerosol formation pathway could account for ∼5.0 Tg yr(-1) of SOA production, or 3.3% of global SOA.

An investigation of South Pole HOx chemistry: Comparison of model results with ISCAT observations

Author(s): Chen, G; Davis, D; Crawford, J; Nowak, JB; Eisele, F; Mauldin, RL; Tanner, D; Buhr, M; Shetter, R; Lefer, B; Arimoto, R; Hogan, A; Blake, D | Abstract: Unexpected high levels of OH and NO were recorded at the South Pole (SP) Atmospheric Research Observatory during the 1998-99 ISCAT field study. Model simulations suggest a major photochemical linkage between observed OH and NO. A detailed comparison of the observations with model predictions revealed good agreement for OH at NO levels between 120 and 380 pptv. However, the model tended to overestimate OH for NO levels l 120 pptv, while it underestimated OH at levels g 380 pptv. The reasons for these deviations appear not to involve NO directly but rather HOx radical scavenging for the low NO conditions and additional HOx sources for the high NO conditions. Because of the elevated levels of NO and highly activated HOx photochemistry, the SP was found to be a strong net source of surface ozone. It is quite likely that the strong oxidizing environment found at the South Pole extends over the entire polar plateau.

Measurement of peroxycarboxylic nitric anhydrides (PANs) during the ITCT 2K2 aircraft intensive experiment

[1] Measurements of peroxycarboxylic nitric anhydrides (PANs), peroxyacetic nitric anhydride (CH3C(O)OONO2; PAN), and peroxypropionic nitric anhydride (CH3CH2C(O)OONO2; PPN) were made in the spring of 2002, off the west coast of North America, as part of the Intercontinental Transport and Chemical Transformation 2002 (ITCT 2K2) project. Long-range transport of Asian emissions was observed in which PAN and PPN mixing ratios were as high as 650 pptv and 90 pptv, respectively. Moreover, these two species constituted as much as 80% of the odd nitrogen (NOy) in those air masses, and median PAN/NOy was more than 60% at altitudes of 4 km and above. Systematic differences in the ratio of PPN to PAN were observed in air masses that had been impacted by Asian urban emissions relative to those impacted by biomass burning. Mixing ratios of PAN and PPN were also elevated in the marine boundary layer close to the west coast of California, possibly because of photochemical production driven by maritime NOx emissions. INDEX TERMS: 0368 Atmospheric Composition and Structure: Troposphere—constituent transport and chemistry; 0365 Atmospheric Composition and Structure: Troposphere—composition and chemistry; 0345 Atmospheric Composition and Structure: Pollution—urban and regional (0305); KEYWORDS: peroxyacetic nitric anhydride, Asian pollution, eastern Pacific

Air quality implications of the Deepwater Horizon oil spill

During the Deepwater Horizon (DWH) oil spill, a wide range of gas and aerosol species were measured from an aircraft around, downwind, and away from the DWH site. Additional hydrocarbon measurements were made from ships in the vicinity. Aerosol particles of respirable sizes were on occasions a significant air quality issue for populated areas along the Gulf Coast. Yields of organic aerosol particles and emission factors for other atmospheric pollutants were derived for the sources from the spill, recovery, and cleanup efforts. Evaporation and subsequent secondary chemistry produced organic particulate matter with a mass yield of 8 ± 4% of the oil mixture reaching the water surface. Approximately 4% by mass of oil burned on the surface was emitted as soot particles. These yields can be used to estimate the effects on air quality for similar events as well as for this spill at other times without these data. Whereas emission of soot from burning surface oil was large during the episodic burns, the mass flux of secondary organic aerosol to the atmosphere was substantially larger overall. We use a regional air quality model to show that some observed enhancements in organic aerosol concentration along the Gulf Coast were likely due to the DWH spill. In the presence of evaporating hydrocarbons from the oil, NOx emissions from the recovery and cleanup operations produced ozone.

An investigation of ammonia and inorganic particulate matter in California during the CalNex campaign

Airborne observations from the California Research at the Nexus of Air Quality and Climate Change (CalNex) campaign in May and June 2010 are used to investigate the role of ammonia (NH3) in fine particulate matter (PM2.5) formation and surface air quality in California and test the key processes relevant to inorganic aerosol formation in the GEOS-Chem model. Concentrations of ammonia throughout California, sulfur dioxide (SO2) in the Central Valley, and ammonium nitrate in the Los Angeles (LA) area are underestimated several-fold in the model. We find that model concentrations are relatively insensitive to uncertainties in gas-particle partitioning and deposition processes in the region. Conversely, increases to anthropogenic livestock ammonia emissions (by a factor of 5) and anthropogenic sulfur dioxide emissions in the Central Valley (by a factor of 3–10) and a reduction of anthropogenic NOx emissions (by 30%) substantially reduce the bias in the simulation of gases (SO2, NH3, HNO3) throughout California and PM2.5 near LA, although the exact magnitudes of emissions in the region remain uncertain. Using these modified emissions, we investigate year-round PM2.5 air quality in California. The model reproduces the wintertime maximum in surface ammonium nitrate concentrations in the Central Valley (regional mean concentrations are three times higher in December than in June), associated with lower planetary boundary layer heights and colder temperatures, and the wintertime minimum in the LA region (regional mean concentrations are two times higher in June than December) associated with ammonia limitation. Year round, we attribute at least 50% of the inorganic PM2.5 mass simulated throughout California to anthropogenic ammonia emissions.

Instrumentation and Measurement Strategy for the NOAA SENEX Aircraft Campaign as Part of the Southeast Atmosphere Study 2013

Natural emissions of ozone-and-aerosol-precursor gases such as isoprene and monoterpenes are high in the southeast of the US. In addition, anthropogenic emissions are significant in the Southeast US and summertime photochemistry is rapid. The NOAA-led SENEX (Southeast Nexus) aircraft campaign was one of the major components of the Southeast Atmosphere Study (SAS) and was focused on studying the interactions between biogenic and anthropogenic emissions to form secondary pollutants. During SENEX, the NOAA WP-3D aircraft conducted 20 research flights between 27 May and 10 July 2013 based out of Smyrna, TN. Here we describe the experimental approach, the science goals and early results of the NOAA SENEX campaign. The aircraft, its capabilities and standard measurements are described. The instrument payload is summarized including detection limits, accuracy, precision and time resolutions for all gas-and-aerosol phase instruments. The inter-comparisons of compounds measured with multiple instruments on the NOAA WP-3D are presented and were all within the stated uncertainties, except two of the three NO2 measurements. The SENEX flights included day- and nighttime flights in the Southeast as well as flights over areas with intense shale gas extraction (Marcellus, Fayetteville and Haynesville shale). We present one example flight on 16 June 2013, which was a daytime flight over the Atlanta region, where several crosswind transects of plumes from the city and nearby point sources, such as power plants, paper mills and landfills, were flown. The area around Atlanta has large biogenic isoprene emissions, which provided an excellent case for studying the interactions between biogenic and anthropogenic emissions. In this example flight, chemistry in and outside the Atlanta plumes was observed for several hours after emission. The analysis of this flight showcases the strategies implemented to answer some of the main SENEX science questions.