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Increasing synoptic scale variability in atmospheric CO2 at Hateruma Island associated with increasing East-Asian emissions

In-situ observations of atmospheric CO2 and CH4 at Hateruma Island (24.05° N, 123.80° E, 47 m a.s.l), Japan shows large synoptic scale variations during a 6-month period from November to April, when the sampled air is predominantly of continental origin due to the Asian winter monsoon. Synoptic scale variations are extracted from the daily averaged values for the years between 1996 and 2007, along with the annual standard deviations (σCO2 and σCH4 for CO2 and CH4, respectively) for the relevant 6-month period. During this 6-month period the absolute mixing ratios of CO2 and CH4 at Hateruma are also elevated compared to those at two sites in the central North Pacific Ocean. The temporal change in σCO2 shows a systematic increase over the 12-year period, with elevated excursions in 1998 and 2003; there is no clear increase in σCH4. We also find that the σCO2/σCH4 ratio increases gradually from 1996 to 2002 and rapidly after 2002 without any extreme deviations that characterised σCO2. The σCO2/σCH4 ratio correlates closely with the recent rapid increase in fossil carbon emissions from China, as indicated in the Carbon Dioxide Information Analysis Center (CDIAC) database. This methodology can be applied to multiple chemical tracers of sufficient lifetime, for tracking overall changes in regional emissions.
Atmospheric sub-3 nm particles at high altitudes

Formation of new atmospheric aerosol particles is known to occur almost all over the world and the importance of these particles to climate and air quality has been recognized. Recently, it was found that atmospheric aerosol particle formation begins at the diameter of around 1.5–2.0 nm and a pool of sub-3 nm atmospheric particles – consisting of both charged and uncharged ones – was observed at the ground level. Here, we report on the first airborne observations of the pool of sub-3 nm neutral atmospheric particles. Between 2 and 3 nm, their concentration is roughly two orders of magnitude larger than that of the ion clusters, depending slightly on the altitude. Our findings indicate that new particle formation takes place throughout the tropospheric column up to the tropopause. Particles were found to be formed via neutral pathways in the boundary layer, and there was no sign of an increasing role by ion-induced nucleation toward the upper troposphere. Clouds, while acting as a source of sub-10 nm ions, did not perturb the overall budget of atmospheric clusters or particles.
Advective mixing in a nondivergent barotropic hurricane model

This paper studies Lagrangian mixing in a two-dimensional barotropic model for hurricane-like vortices. Since such flows show high shearing in the radial direction, particle separation across shear-lines is diagnosed through a Lagrangian field, referred to as R-field, that measures trajectory separation orthogonal to the Lagrangian velocity. The shear-lines are identified with the level-contours of another Lagrangian field, referred to as S-field, that measures the average shear-strength along a trajectory. Other fields used for model diagnostics are the Lagrangian field of finite-time Lyapunov exponents (FTLE-field), the Eulerian Q-field, and the angular velocity field. Because of the high shearing, the FTLE-field is not a suitable indicator for advective mixing, and in particular does not exhibit ridges marking the location of finite-time stable and unstable manifolds. The FTLE-field is similar in structure to the radial derivative of the angular velocity. In contrast, persisting ridges and valleys can be clearly recognized in the R-field, and their propagation speed indicates that transport across shear-lines is caused by Rossby waves. A radial mixing rate derived from the R-field gives a time-dependent measure of flux across the shear-lines. On the other hand, a measured mixing rate across the shear-lines, which counts trajectory crossings, confirms the results from the R-field mixing rate, and shows high mixing in the eyewall region after the formation of a polygonal eyewall, which continues until the vortex breaks down. The location of the R-field ridges elucidates the role of radial mixing for the interaction and breakdown of the mesovortices shown by the model.
Kinetics and mechanisms of heterogeneous reaction of NO2 on CaCO3 surfaces under dry and wet conditions

With increasing NO2 concentration in the troposphere, the importance of NO2 reaction with mineral dust in the atmosphere needs to be evaluated. Until now, little is known about the reaction of NO2 with CaCO3. In this study, the heterogeneous reaction of NO2 on the surface of CaCO3 particles was investigated at 296 K and NO2 concentrations between 4.58×1015 molecules cm−3 to 1.68×1016 molecules cm−3, using diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) combined with X-ray photoelectron spectroscopy (XPS) and scanning electron microscopy (SEM), under wet and dry conditions. Nitrate formation was observed under both conditions, while nitrite was observed under wet conditions, indicating the reaction of NO2 on the CaCO3 surface produced nitrate and probably nitrous acid (HONO). Relative humidity (RH) influences both the initial uptake coefficient and the reaction mechanism. At low RH, surface −OH is formed through dissociation of the surface adsorbed water via oxygen vacancy, thus determining the reaction order. As RH increases, water starts to condense on the surface and the gas-liquid reaction of NO2 with the condensed water begins. With high enough RH (>52% in our experiment), the gas-liquid reaction of NO2 with condensed water becomes dominant, forming HNO3 and HONO. The initial uptake coefficient γ0 was determined to be (4.25±1.18)×10−9 under dry conditions and up to (6.56±0.34)×10−8 under wet conditions. These results suggest that the reaction of NO2 on CaCO3 particle is unable to compete with that of HNO3 in the atmosphere. Further studies at lower NO2 concentrations and with a more accurate assessment of the surface area for calculating the uptake coefficient of the reaction of NO2 on CaCO3 particle and to examine its importance as a source of HONO in the atmosphere are needed.
Forecasted deep stratospheric intrusions over Central Europe: case studies and climatologies

Based on daily predictions of stratospheric air intrusions, obtained from trajectory calculations by ETH Zürich with wind fields from ECMWF forecasts, a high number of measurements with the ozone lidar at IMK-IFU (Garmisch-Partenkirchen, Germany) were carried out in 2001. The lidar measurements show a large variety of rather different cases reflecting the full complexity of intrusion episodes that is not visible in classical case studies. In part, tropopause folds could be fully captured. The frequency of intrusion cases forecasted and verified by vertical sounding or in the in-situ data recorded at the nearby Zugspitze summit (2962 m a.s.l.) exceed that in previous work by more than a factor of two. Three cases mapped with the lidar were selected to validate the results for the corresponding time periods extracted from a one-year run with the new hemispheric version of the chemistry-transport model EURAD. Due to the high spatial resolution chosen for these simulations the agreement with the lidar measurements is satisfactory. The Zugspitze ozone data from 1978 to 2004 were recently filtered by applying different criteria for stratospheric air, based on the 7Be and humidity measurements. Here, by using the daily model forecasts during the time period 2001–2005, we examine three criteria and determine how well they represent the stratospheric air intrusions reaching the mountain site. Seasonal cycles for the period 2001–2005 were derived for the forecasts as well as the intrusion frequency per month for the forecasted intrusions and each of the criteria, distinguishing eight different characteristic transport pathways. In most cases a winter maximum and a summer minimum was obtained, but in the case of cyclonic arrival of intrusions starting over Greenland a late-spring maximum is seen. Two of the filtering criteria examined, based on combining a relative-humidity (RH) threshold of 60% with either a 7Be threshold of 5.5 mBq m−3 or the requirement for RH≤30% within ±6 h, rather reliably predict periods of deep intrusions reaching the Zugspitze station. An "or" combination of both these criteria yields slightly more cases and covers 77.9% of the intrusions identified. The lack of observations in the complementary 22.1% are mostly explained by overpasses. In this way the long-term trend of stratospheric ozone observed at this site as well as the corresponding ozone budget may be derived on the basis of measurements only. This effort will be the subject of a subsequent publication.
Evaluation of the volatility basis-set approach for the simulation of organic aerosol formation in the Mexico City metropolitan area

New primary and secondary organic aerosol modules have been added to PMCAMx, a three dimensional chemical transport model (CTM), for use with the SAPRC99 chemistry mechanism based on recent smog chamber studies. The new modelling framework is based on the volatility basis-set approach: both primary and secondary organic components are assumed to be semivolatile and photochemically reactive and are distributed in logarithmically spaced volatility bins. This new framework with the use of the new volatility basis parameters for low-NOx and high-NOx conditions tends to predict 4–6 times higher anthropogenic SOA concentrations than those predicted with the older generation of models. The resulting PMCAMx-2008 was applied in Mexico City Metropolitan Area (MCMA) for approximately a week during April 2003 during a period of very low regional biomass burning impact. The emission inventory, which uses as a starting point the MCMA 2004 official inventory, is modified and the primary organic aerosol (POA) emissions are distributed by volatility based on dilution experiments. The predicted organic aerosol (OA) concentrations peak in the center of Mexico City, reaching values above 40 μg m−3. The model predictions are compared with the results of the Positive Matrix Factorization (PMF) analysis of the Aerosol Mass Spectrometry (AMS) observations. The model reproduces both Hydrocarbon-like Organic Aerosol (HOA) and Oxygenated Organic Aerosol (OOA) concentrations and diurnal profiles. The small OA underprediction during the rush-hour periods and overprediction in the afternoon suggest potential improvements to the description of fresh primary organic emissions and the formation of the oxygenated organic aerosols, respectively, although they may also be due to errors in the simulation of dispersion and vertical mixing. However, the AMS OOA data are not specific enough to prove that the model reproduces the organic aerosol observations for the right reasons. Other combinations of contributions of primary and secondary organic aerosol production rates may lead to similar results. The model results strongly suggest that, during the simulated period, transport of OA from outside the city was a significant contributor to the observed OA levels. Future simulations should use a larger domain in order to test whether the regional OA can be predicted with current SOA parameterizations. Sensitivity tests indicate that the predicted OA concentration is especially sensitive to the volatility distribution of the emissions in the lower volatility bins.
Technical Note: Sensitivity of 1-D smoke plume rise models to the inclusion of environmental wind drag

Vegetation fires emit hot gases and particles which are rapidly transported upward by the positive buoyancy generated by the combustion process. In general, the final vertical height that the smoke plumes reach is controlled by the thermodynamic stability of the atmospheric environment and the surface heat flux released by the fire. However, the presence of a strong horizontal wind can enhance the lateral entrainment and induce additional drag, particularly for small fires, impacting the smoke injection height. In this paper, we revisit the parameterization of the vertical transport of hot gases and particles emitted from vegetation fires, described in Freitas et al. (2007), to include the effects of environmental wind on transport and dilution of the smoke plume at its scale. This process is quantitatively represented by introducing an additional entrainment term to account for organized inflow of a mass of cooler and drier ambient air into the plume and its drag by momentum transfer. An extended set of equations including the horizontal motion of the plume and the additional increase of the plume radius is solved to simulate the time evolution of the plume rise and the smoke injection height. One-dimensional (1-D) model results are presented for two deforestation fires in the Amazon basin with sizes of 10 and 50 ha under calm and windy atmospheric environments. The results are compared to corresponding simulations generated by the complex non-hydrostatic three-dimensional (3-D) Active Tracer High resolution Atmospheric Model (ATHAM). We show that the 1-D model results compare well with the full 3-D simulations. The 1-D model may thus be used in field situations where extensive computing facilities are not available, especially under conditions for which several optional cases must be studied.
Corrigendum to "Overview: oxidant and particle photochemical processes above a south-east Asian tropical rainforest (the OP3 project): introduction, rationale, location characteristics and tools" published in Atmos. Chem. Phys., 10, 169–199, 2010
Carbonyl sulfide exchange in a temperate loblolly pine forest grown under ambient and elevated CO2

Vegetation, soil and ecosystem level carbonyl sulfide (COS) exchange was observed at Duke Forest, a temperate loblolly pine forest, grown under ambient (Ring 1, R1) and elevated (Ring 2, R2) CO2. During calm meteorological conditions, ambient COS mixing ratios at the top of the forest canopy followed a distinct diurnal pattern in both CO2 growth regimes, with maximum COS mixing ratios during the day (R1=380±4 pptv and R2=373±3 pptv, daytime mean ± standard error) and minimums at night (R1=340±6 pptv and R2=346±5 pptv, nighttime mean ± standard error) reflecting a significant nighttime sink. Nocturnal vegetative uptake (−11 to −21 pmol m−2s−1, negative values indicate uptake from the atmosphere) dominated nighttime net ecosystem COS flux estimates (−10 to −30 pmol m−2s−1) in both CO2 regimes. In comparison, soil uptake (−0.8 to −1.7 pmol m−2 s−1) was a minor component of net ecosystem COS flux. In both CO2 regimes, loblolly pine trees exhibited substantial COS consumption overnight (50% of daytime rates) that was independent of CO2 assimilation. This suggests current estimates of the global vegetative COS sink, which assume that COS and CO2 are consumed simultaneously, may need to be reevaluated. Ambient COS mixing ratios, species specific diurnal patterns of stomatal conductance, temperature and canopy position were the major factors influencing the vegetative COS flux at the branch level. While variability in branch level vegetative COS consumption measurements in ambient and enhanced CO2 environments could not be attributed to CO2 enrichment effects, estimates of net ecosystem COS flux based on ambient canopy mixing ratio measurements suggest less nighttime uptake of COS in R2, the CO2 enriched environment.
Trace gas and particle emissions from domestic and industrial biofuel use and garbage burning in central Mexico

In central Mexico during the spring of 2007 we measured the initial emissions of 12 gases and the aerosol speciation for elemental and organic carbon (EC, OC), anhydrosugars, Cl−, NO3−, and 20 metals from 10 cooking fires, four garbage fires, three brick making kilns, three charcoal making kilns, and two crop residue fires. Global biofuel use has been estimated at over 2600 Tg/y. With several simple case studies we show that cooking fires can be a major, or the major, source of several gases and fine particles in developing countries. Insulated cook stoves with chimneys were earlier shown to reduce indoor air pollution and the fuel use per cooking task. We confirm that they also reduce the emissions of VOC pollutants per mass of fuel burned by about half. We did not detect HCN emissions from cooking fires in Mexico or Africa. Thus, if regional source attribution is based on HCN emissions typical for other types of biomass burning (BB), then biofuel use and total BB will be underestimated in much of the developing world. This is also significant because cooking fires are not detected from space. We estimate that ~2000 Tg/y of garbage are generated globally and about half may be burned, making this a commonly overlooked major global source of emissions. We estimate a fine particle emission factor (EFPM2.5) for garbage burning of ~10.5±8.8 g/kg, which is in reasonable agreement with very limited previous work. We observe large HCl emission factors in the range 2–10 g/kg. Consideration of the Cl content of the global waste stream suggests that garbage burning may generate as much as 6–9 Tg/yr of HCl, which would make it a major source of this compound. HCl generated by garbage burning in dry environments may have a relatively greater atmospheric impact than HCl generated in humid areas. Garbage burning PM2.5 was found to contain levoglucosan and K in concentrations similar to those for biomass burning, so it could be a source of interference in some areas when using these tracers to estimate BB. Galactosan was the anhydrosugar most closely correlated with BB in this study. Fine particle antimony (Sb) shows initial promise as a garbage burning tracer and suggests that this source could contribute a significant amount of the PM2.5 in the Mexico City metropolitan area. The fuel consumption and emissions due to industrial biofuel use are difficult to characterize regionally. This is partly because of the diverse range of fuels used and the very small profit margins of typical micro-enterprises. Brick making kilns produced low total EFPM2.5 (~1.6 g/kg), but very high EC/OC ratios (6.72). Previous literature on brick kilns is scarce but does document some severe local impacts. Coupling data from Mexico, Brazil, and Zambia, we find that charcoal making kilns can exhibit an 8-fold increase in VOC/CO over their approximately one-week lifetime. Acetic acid emission factors for charcoal kilns were much higher in Mexico than elsewhere. Our dirt charcoal kiln EFPM2.5 emission factor was ~1.1 g/kg, which is lower than previous recommendations intended for all types of kilns. We speculate that some PM2.5 is scavenged in the walls of dirt kilns.