Introducing the concept of Potential Aerosol Mass (PAM)

International audiencePotential Aerosol Mass (PAM) can be defined as the maximum aerosol mass that the oxidation of precursor gases produces. In the measurement, all precursor gases are rapidly oxidized with extreme amounts of oxidants to low volatility compounds, resulting in the aerosol formation. Oxidation occurs in a small, simple, flow-through chamber that has a short residence time and is irradiated with ultraviolet light. The amount of the oxidants ozone (O3), hydroxyl (OH), and hydroperoxyl (HO2) were measured directly and can be controlled by varying the UV light and the relative humidity. Maximum values were 40 ppmv for O3 500 pptv for OH, and 4 ppbv for HO2. The oxidant amounts are 100 to 1000 times troposphere values, but the ratios OH/O3 and HO2/OH are similar to troposphere values. The aerosol production mechanism and the aerosol mass yield were studied for several controlling variables, such as temperature, relative humidity, oxidant concentration, presence of nitrogen oxides (NOx), precursor gas composition and amount, and the presence of acidic seed aerosol. The measured secondary organic aerosol (SOA) yield of several natural and anthropogenic volatile organic compounds and a mixture of hydrocarbons in the PAM chamber were similar to those obtained in large, batch-style environmental chambers. This PAM method is being developed for measuring potential aerosol mass in the atmosphere, but is also useful for examining SOA processes in the laboratory and in environmental chambers

Measurements of quantum yields of bromine atoms in the photolysis of bromoform from 266 to 324 nm

The quantum yield for the formation of bromine atoms in the photolysis of bromoform, CHBr_3, has been measured between 266 and 324 nm. For 303 to 306 nm the quantum yields are unity within the experimental uncertainty of the measurements. At longer wavelengths, where the bromoform cross sections decrease rapidly, an apparent trend to slightly lower quantum yields is probably the result of systematic and random errors or incorrect CHBr_3 absorption cross sections. Support for a unit quantum yield for all wavelengths longer than 300 nm comes from the recent theoretical calculations of Peterson and Francisco. At 266 nm the bromine atom quantum yield is 0.76 (±0.03), indicating that at least one additional dissociation channel becomes important at shorter wavelengths. For modeling of the troposphere, it is recommended that a quantum yield of unity be used for wavelengths of 300 nm and longer

The Role of Small to Moderate Volcanic Eruptions in the Early 19th Century Climate

Small-to-moderate volcanic eruptions can lead to significant surface cooling when they occur clustered, as observed in recent decades. In this study, based on new high-resolution ice-core data from Greenland, we produce a new volcanic forcing data set that includes several small-to-moderate eruptions not included in prior reconstructions and investigate their climate impacts of the early 19th century through ensemble simulations with the Max Planck Institute Earth System Model. We find that clustered small-to-moderate eruptions produce significant additional global surface cooling (∼0.07 K) during the period 1812–1820, superposing with the cooling by large eruptions in 1809 (unidentified location) and 1815 (Tambora). This additional cooling helps explain the reconstructed long-lasting cooling after the large eruptions, but simulated regional impacts cannot be confirmed with reconstructions due to a low signal-to-noise ratio. This study highlights the importance of small-to-moderate eruptions for climate simulations as their impacts can be comparable with that of solar irradiance changes

Introducing the concept of Potential Aerosol Mass (PAM)

La Constitución Política de Colombia de 1991 intentó consolidar un proceso de cambio cultural tendiente a modernizar la administración pública haciendo más eficaces, eficientes y económicos los procedimientos de gobierno y por consiguiente, el desempeño de los empleados oficiales

A fiber-coupled laser hygrometer for airborne total water measurement

The second-generation University of Colorado closed-path tunable-diode laser hygrometer (CLH-2) is an instrument for the airborne in situ measurement of total water content – the sum of vapor-, liquid- and ice-phase water – in clouds. This compact instrument has been flown on the NSF/NCAR Gulfstream-V aircraft in an underwing canister. It operates autonomously and uses fiber-coupled optics to eliminate the need for a supply of dry compressed gas. In operation, sample air is ingested into a forward-facing sub-isokinetic inlet; this sampling configuration results in particle concentrations that are enhanced relative to ambient and causes greater instrument sensitivity to condensed water particles. Heaters within the inlet vaporize the ingested water particles, and the resulting augmented water vapor mixing ratio is measured by absorption of near-infrared light in a single-pass optical cell. The condensed water content is then determined by subtracting the ambient water vapor content from the total and by accounting for the inertial enhancement of particles into the sampling inlet. The CLH-2 is calibrated in the laboratory over a range of pressures and water vapor mixing ratios; the uncertainty in CLH-2 condensed water retrievals is estimated to be 14.3% to 16.1% (1-σ). A vapor-only laboratory intercomparison with the first-generation University of Colorado closed-path tunable-diode laser hygrometer (CLH) shows agreement within the 2-σ uncertainty bounds of both instruments

Isoprene oxidation products are a significant atmospheric aerosol component

International audienceGlycolaldehyde, hydroxyacetone, and methylglyoxal, which are known isoprene oxidation products, were collected during two field experiments using an annular denuder sampling system and compared to a model calculation. The compounds in gas and aerosol phases were determined during both experiments. Global variation and distribution of the aerosol mass contribution of the compounds were predicted using the measurements, the box model results, and gas-phase concentrations and humidity simulated by a global 3-D model. Here we report the estimates of a global annual contribution of 35 (10?120) Tg of aerosol organic matter from isoprene

Ozone loss derived from balloon-borne tracer measurements in the 1999/2000 Arctic winter

Balloon-borne measurements of CFC11 (from the DIRAC in situ gas chromatograph and the DESCARTES grab sampler), ClO and O3 were made during the 1999/2000 Arctic winter as part of the SOLVE-THESEO 2000 campaign, based in Kiruna (Sweden). Here we present the CFC11 data from nine flights and compare them first with data from other instruments which flew during the campaign and then with the vertical distributions calculated by the SLIMCAT 3D CTM. We calculate ozone loss inside the Arctic vortex between late January and early March using the relation between CFC11 and O3 measured on the flights. The peak ozone loss (~1200ppbv) occurs in the 440-470K region in early March in reasonable agreement with other published empirical estimates. There is also a good agreement between ozone losses derived from three balloon tracer data sets used here. The magnitude and vertical distribution of the loss derived from the measurements is in good agreement with the loss calculated from SLIMCAT over Kiruna for the same days

Measurements of quantum yields of bromine atoms in the photolysis of bromoform from 266 to 324 nm

The quantum yield for the formation of bromine atoms in the photolysis of bromoform, CHBr_3, has been measured between 266 and 324 nm. For 303 to 306 nm the quantum yields are unity within the experimental uncertainty of the measurements. At longer wavelengths, where the bromoform cross sections decrease rapidly, an apparent trend to slightly lower quantum yields is probably the result of systematic and random errors or incorrect CHBr_3 absorption cross sections. Support for a unit quantum yield for all wavelengths longer than 300 nm comes from the recent theoretical calculations of Peterson and Francisco. At 266 nm the bromine atom quantum yield is 0.76 (±0.03), indicating that at least one additional dissociation channel becomes important at shorter wavelengths. For modeling of the troposphere, it is recommended that a quantum yield of unity be used for wavelengths of 300 nm and longer

Emissions from biomass burning in the Yucatan

In March 2006 two instrumented aircraft made the first detailed field measurements of biomass burning (BB) emissions in the Northern Hemisphere tropics as part of the MILAGRO project. The aircraft were the National Center for Atmospheric Research C-130 and a University of Montana/US Forest Service Twin Otter. The initial emissions of up to 49 trace gas or particle species were measured from 20 deforestation and crop residue fires on the Yucatan peninsula. This included two trace gases useful as indicators of BB (HCN and acetonitrile) and several rarely, or never before, measured species: OH, peroxyacetic acid, propanoic acid, hydrogen peroxide, methane sulfonic acid, and sulfuric acid. Crop residue fires emitted more organic acids and ammonia than deforestation fires, but the emissions from the main fire types were otherwise fairly similar. The Yucatan fires emitted unusually high amounts of SO2 and particle chloride, likely due to a strong marine influence on this peninsula. As smoke from one fire aged, the ratio ΔO3/ΔCO increased to ~15% in 1×10^7 molecules/cm^3) that were likely caused in part by high initial HONO (~10% of NO_y). Thus, more research is needed to understand critical post emission processes for the second-largest trace gas source on Earth. It is estimated that ~44 Tg of biomass burned in the Yucatan in the spring of 2006. Mexican BB (including Yucatan BB) and urban emissions from the Mexico City area can both influence the March-May air quality in much of Mexico and the US

Ozone loss derived from balloon-borne tracer measurements and the SLIMCAT CTM

Balloon-borne measurements of CFC-11 (on flights of the DIRAC in situ gas chromatograph and the DESCARTES grab sampler), ClO and O3 were made during the 1999/2000 winter as part of the SOLVE-THESEO 2000 campaign. Here we present the CFC-11 data from nine flights and compare them first with data from other instruments which flew during the campaign and then with the vertical distributions calculated by the SLIMCAT 3-D CTM. We calculate ozone loss inside the Arctic vortex between late January and early March using the relation between CFC-11 and O3 measured on the flights, the peak ozone loss (1200 ppbv) occurs in the 440–470 K region in early March in reasonable agreement with other published empirical estimates. There is also a good agreement between ozone losses derived from three independent balloon tracer data sets used here. The magnitude and vertical distribution of the loss derived from the measurements is in good agreement with the loss calculated from SLIMCAT over Kiruna for the same days