ALBERT

Description: Photooxidation products of biogenic volatile organic compounds, mainly isoprene and monoterpenes, are significant sources of atmospheric particulate matter in forested regions. The objectives of this study were to examine time trends and diurnal variations of polar organic tracers for the photooxidation of isoprene and α-pinene to investigate whether they are linked with meteorological parameters or trace gases and to estimate their regional carbon contributions. PM2.5 (particulate matter with an aerodynamic diameter

Description: The sulfur cycle and radiative effects of sulfate aerosol on climate are studied with a Global tropospheric Climate-Chemistry Model in which chemistry, radiation and dynamics are fully coupled. Production and removal mechanisms of sulfate are analyzed for the conditions of natural and anthropogenic sulfur emissions. Results show that the 1985 anthropogenic emission doubled the global SO2 and sulfate loadings from its natural value of 0.15 and 0.27 Tg S, respectively. Under natural conditions, the fraction of sulfate produced in-cloud is 87%, and the lifetime of SO2 and sulfate are 1.8 and 4.0 days, respectively; whereas with anthropogenic emissions, changes in in-cloud sulfate production are small, while SO2 and sulfate lifetimes are significant reduced (1.0 and 2.4 days, respectively). The doubling of sulfate results in a direct radiative forcing of −0.32 and −0.14 W m−2 under clear-sky and all-sky conditions, respectively, and a significant first indirect forcing of −1.69 W m−2. The first indirect forcing is sensitive to the relationship between aerosol concentration and cloud droplet number concentration. Two aspects of chemistry-climate interaction are addressed. Firstly, the coupling effects lead to 10% and 2% decreases in sulfate loading, respectively, for the cases of natural and anthropogenic added sulfur emissions. Secondly, only the indirect effect of sulfate aerosols yields significantly stronger signals in changes of near surface temperature and sulfate loading than changes due to intrinsic climate variability, while other responses to the indirect effect and all responses to the direct effect are weak.

Description: The Tibetan Plateau (TP), the highest and largest plateau in the world, has long been identified to be critical in regulating the Asian monsoon climate and hydrological cycle. The snowpack and glaciers over the TP provide fresh water to billions of people in Asian countries, but the TP glaciers have been retreating faster than those anywhere else in the world. In this modeling study a series of numerical experiments with a global climate model are designed to simulate radiative forcing of black carbon (BC) and dust in snow, and to assess the relative impacts of anthropogenic CO2 and carbonaceous particles in the atmosphere and snow on the snowpack over the TP and subsequent impacts on the Asian monsoon climate and hydrological cycle. Simulations results show a large BC content in snow over the TP, especially the southern slope, with concentration larger than 100 μg/kg. Because of the high aerosol content in snow and large incident solar radiation in the low latitude and high elevation, the TP exhibits the largest surface radiative forcing induced by aerosols (e.g. BC, Dust) in snow compared to other snow-covered regions in the world. Simulation results show that the aerosol-induced snow albedo perturbations generate surface radiative forcing of 5–25 W m−2 during spring, with a maximum in April or May. BC-in-snow increases the surface air temperature by around 1.0 °C averaged over the TP and reduces spring snowpack over the TP more than pre-industrial to present CO2 increase and carbonaceous particles in the atmosphere. As a result, runoff increases during late winter and early spring but decreases during late spring and early summer (i.e. a trend toward earlier melt dates). The snowmelt efficacy, defined as the snowpack reduction per unit degree of warming induced by the forcing agent, is 1–4 times larger for BC-in-snow than CO2 increase during April–July, indicating that BC-in-snow more efficiently accelerates snowmelt because the increased net solar radiation induced by reduced albedo melts the snow more efficiently than snow melt due to warming in the air. The TP also influences the South (SAM) and East (EAM) Asian monsoon through its dynamical and thermal forcing. Simulation results show that during boreal spring aerosols are transported by southwesterly, causing some particles to reach higher altitude and deposit to the snowpack over the TP. While BC and OM in the atmosphere directly absorb sunlight and warm the air, the darkened snow surface polluted by BC absorbs more solar radiation and increases the skin temperature, which warms the air above through sensible heat flux. Both effects enhance the upward motion of air and spur deep convection along the TP during the pre-monsoon season, resulting in earlier onset of the SAM and increase of moisture, cloudiness and convective precipitation over Northern India. BC-in-snow has a more significant impact on the EAM in July than CO2 increase and carbonaceous particles in the atmosphere. Contributed by the significant increase of both sensible heat flux associated with the warm skin temperature and latent heat flux associated with increased soil moisture with long memory, the role of the TP as a heat pump is elevated from spring through summer as the land-sea thermal contrast increases to strengthen the EAM. As a result, both Southern China and Northern China become wetter, but Central China (i.e. Yangtze River Basin) becomes drier – a near-zonal anomaly pattern that is consistent with the dominant mode of precipitation variability in East Asia.

Description: The Tibetan Plateau (TP) has long been identified to be critical in regulating the Asian monsoon climate and hydrological cycle. In this modeling study a series of numerical experiments with a global climate model are designed to simulate radiative effect of black carbon (BC) and dust in snow, and to assess the relative impacts of anthropogenic CO2 and carbonaceous particles in the atmosphere and snow on the snowpack over the TP and subsequent impacts on the Asian monsoon climate and hydrological cycle. Simulations results show a large BC content in snow over the TP, especially the southern slope. Because of the high aerosol content in snow and large incident solar radiation in the low latitude and high elevation, the TP exhibits the largest surface radiative flux changes induced by aerosols (e.g. BC, Dust) in snow compared to any other snow-covered regions in the world. Simulation results show that the aerosol-induced snow albedo perturbations generate surface radiative flux changes of 5–25 W m−2 during spring, with a maximum in April or May. BC-in-snow increases the surface air temperature by around 1.0 °C averaged over the TP and reduces spring snowpack over the TP more than pre-industrial to present CO2 increase and carbonaceous particles in the atmosphere. As a result, runoff increases during late winter and early spring but decreases during late spring and early summer (i.e. a trend toward earlier melt dates). The snowmelt efficacy, defined as the snowpack reduction per unit degree of warming induced by the forcing agent, is 1–4 times larger for BC-in-snow than CO2 increase during April–July, indicating that BC-in-snow more efficiently accelerates snowmelt because the increased net solar radiation induced by reduced albedo melts the snow more efficiently than snow melt due to warming in the air. The TP also influences the South (SAM) and East (EAM) Asian monsoon through its dynamical and thermal forcing. Simulation results show that during boreal spring aerosols are transported by southwesterly, causing some particles to reach higher altitude and deposit to the snowpack over the TP. While BC and Organic Matter (OM) in the atmosphere directly absorb sunlight and warm the air, the darkened snow surface polluted by BC absorbs more solar radiation and increases the skin temperature, which warms the air above through sensible heat flux. Both effects enhance the upward motion of air and spur deep convection along the TP during the pre-monsoon season, resulting in earlier onset of the SAM and increase of moisture, cloudiness and convective precipitation over northern India. BC-in-snow has a more significant impact on the EAM in July than CO2 increase and carbonaceous particles in the atmosphere. Contributed by the significant increase of both sensible heat flux associated with the warm skin temperature and latent heat flux associated with increased soil moisture with long memory, the role of the TP as a heat pump is elevated from spring through summer as the land-sea thermal contrast increases to strengthen the EAM. As a result, both southern China and northern China become wetter, but central China (i.e. Yangtze River Basin) becomes drier – a near-zonal anomaly pattern that is consistent with the dominant mode of precipitation variability in East Asia. The snow impurity effects reported in this study likely represent some upper limits as snowpack is remarkably overestimated over the TP due to excessive precipitation. Improving the simulation of precipitation and snowpack will be important for improved estimates of the effects of snowpack pollution in future work.

Description: Total atmospheric OH reactivities (kOH) have been measured as reciprocal OH lifetimes by a newly developed instrument at a rural site in the densely populated Pearl River Delta (PRD) in Southern China in summer 2006. The deployed technique, LP-LIF, uses laser flash photolysis (LP) for artificial OH generation and laser-induced fluorescence (LIF) to measure the time-dependent OH decay in samples of ambient air. The reactivities observed at PRD covered a range from 10 s−1 to 120 s−1, indicating a large load of chemical reactants. On average, kOH exhibited a pronounced diurnal profile with a mean maximum value of 50 s−1 at daybreak and a mean minimum value of 20 s−1 at noon. The comparison of reactivities calculated from measured trace gases with measured kOH reveals a missing reactivity of about a factor of 2 at day and night. The reactivity explained by measured trace gases was dominated by anthropogenic pollutants (e.g., CO, NOx, light alkenes and aromatic hydrocarbons) at night, while it was strongly influenced by local, biogenic emissions of isoprene during the day. Box model calculations initialized by measured parameters reproduce the observed OH reactivity well and suggest that the missing reactivity is contributed by unmeasured, secondary chemistry products (mainly aldehydes and ketones) that were photochemically formed by hydrocarbon oxidation. Overall, kOH was dominated by organic compounds, which had a maximum contribution of 85% in the afternoon. The paper demonstrates the usefulness of direct reactivity measurements, emphasizes the need for direct measurements of oxygenated organic compounds in atmospheric chemistry studies, and discusses uncertainties of the modelling of OVOC reactivities.

Description: An offline-coupled model (WRF/Polyphemus) and an online-coupled model (WRF/Chem-MADRID) are applied to simulate air quality in July 2001 at horizontal grid resolutions of 0.5° and 0.125° over Western Europe. The model performance is evaluated against available surface and satellite observations. The two models simulate different concentrations in terms of domainwide performance statistics, spatial distribution, temporal variations, and column abundance. WRF/Chem-MADRID at 0.5° gives higher values than WRF/Polyphemus for the domainwide mean and over polluted regions in Central and southern Europe for all surface concentrations and column variables except for the tropospheric ozone residual (TOR). Compared with observations, WRF/Polyphemus gives better statistical performance for daily HNO3, SO2, and NO2 at the European Monitoring and Evaluation Programme (EMEP) sites, maximum 1 h O3 at the AirBase sites, PM2.5 at the AirBase sites, maximum 8 h O3 and PM10 composition at all sites, column abundance of CO, NO2, TOR, and aerosol optical depth (AOD), whereas WRF/Chem-MADRID gives better statistical performance for NH3, hourly SO2, NO2, and O3 at the AirBase and BDQA (Base de données de la qualité de l'air) sites, maximum 1 h O3 at the BDQA and EMEP sites, and PM10 at all sites. WRF/Chem-MADRID generally reproduces well the observed high hourly concentrations of SO2 and NO2 at most sites except for extremely high episodes at a few sites, and WRF/Polyphemus performs well for hourly SO2 concentrations at most rural or background sites where pollutant levels are relatively low, but it underpredicts the observed hourly NO2 concentrations at most sites. Both models generally capture well the daytime maximum 8 h O3 concentrations and diurnal variations of O3 with more accurate peak daytime and minimal nighttime values by WRF/Chem-MADRID, but neither model reproduces extremely low nighttime O3 concentrations at several urban and suburban sites due to underpredictions of NOx and thus insufficient titration of O3 at night. WRF/Polyphemus gives more accurate concentrations of PM2.5, and WRF/Chem-MADRID reproduces better the observations of PM10 concentrations at all sites. The differences between model predictions and observations are mostly caused by inaccurate representations of emissions of gaseous precursors and primary PM species, as well as biases in the meteorological predictions. The differences in model predictions are caused by differences in the heights of the first model layers and thickness of each layer that affect vertical distributions of emissions, model treatments such as dry/wet deposition, heterogeneous chemistry, and aerosol and cloud, as well as model inputs such as emissions of soil dust and sea salt and chemical boundary conditions of CO and O3 used in both models. WRF/Chem-MADRID shows a higher sensitivity to grid resolution than WRF/Polyphemus at all sites. For both models, the use of a finer grid resolution generally leads to an overall better statistical performance for most variables, with greater spatial details and an overall better agreement in temporal variations and magnitudes at most sites. The use of online biogenic volatile organic compound (BVOC) emissions gives better statistical performance for hourly and maximum 8 h O3 and PM2.5 and generally better agreement with their observed temporal variations at most sites. Because it is an online model, WRF/Chem-MADRID offers the advantage of accounting for various feedbacks between meteorology and chemical species. However, this model comparison suggests that atmospheric pollutant concentrations are most sensitive in state-of-the-science air quality models to vertical structure, inputs, and parameterizations for dry/wet removal of gases and particles in the model.

Description: This paper presents the first results of the measurements of trace gases and aerosols at three surface sites in and outside Beijing before and during the 2008 Olympics. The official air pollution index near the Olympic Stadium and the data from our nearby site revealed an obvious association between air quality and meteorology and different responses of secondary and primary pollutants to the control measures. Ambient concentrations of vehicle-related nitrogen oxides (NOx) and volatile organic compounds (VOCs) at an urban site dropped by 25% and 20–45% in the first two weeks after full control was put in place, but the levels of ozone, sulfate and nitrate in PM2.5 increased by 16%, 64%, 37%, respectively, compared to the period prior to the full control; wind data and back trajectories indicated the contribution of regional pollution from the North China Plain. Air quality (for both primary and secondary pollutants) improved significantly during the Games, which were also associated with the changes in weather conditions (prolonged rainfall, decreased temperature, and more frequent air masses from clean regions). A comparison of the ozone data at three sites on eight ozone-pollution days, when the air masses were from the southeast-south-southwest sector, showed that regional pollution sources contributed 〉34–88% to the peak ozone concentrations at the urban site in Beijing. Regional sources also contributed significantly to the CO concentrations in urban Beijing. Ozone production efficiencies at two sites were low (~3 ppbv/ppbv), indicating that ozone formation was being controlled by VOCs. Compared with data collected in 2005 at a downwind site, the concentrations of ozone, sulfur dioxide (SO2), total sulfur (SO2+PM2.5 sulfate), carbon monoxide (CO), reactive aromatics (toluene and xylenes) sharply decreased (by 8–64%) in 2008, but no significant changes were observed for the concentrations of PM2.5, fine sulfate, total odd reactive nitrogen (NOy), and longer lived alkanes and benzene. We suggest that these results indicate the success of the government's efforts in reducing emissions of SO2, CO, and VOCs in Beijing, but increased regional emissions during 2005–2008. More stringent control of regional emissions will be needed for significant reductions of ozone and fine particulate pollution in Beijing.

Description: A study of the atmospheric heterogeneous reactions of formic acid, acetic acid, and propionic acid on α-Al2O3 was performed at ambient condition by using a diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) reactor. From the analysis of the spectral features, observations of carboxylates formation provide strong evidence for an efficient reactive uptake process. Comparison of the calculated and experimental vibrational frequencies of adsorbed carboxylates establishes the bridging coordinated structures on the surface. The uptake coefficients of formic acid, acetic acid, and propionic acid on α-Al2O3 particles are (2.07±0.26)×10−3 or (2.37±0.30) ×10−7, (5.00±0.69)×10−3 or (5.99±0.78)×10−7, and (3.04±0.63)×10−3 or (3.03±0.52)×10−7, respectively (using geometric or BET surface area). Furthermore, the effect of varying relative humidity (RH) on these heterogeneous reactions was studied. The uptake coefficients of monocarboxylic acids on α-Al2O3 particles increase initially (RH20%) which was due to the effect of water on carboxylic acid solvation, particle surface hydroxylation, and competition for reactive sites. On the basis of the results of experimental simulation, the mechanism of heterogeneous reaction of α-Al2O3 with carboxylic acids at ambient RH was discussed. The loss of atmospheric monocarboxylic acids due to reactive uptake on available mineral dust particles may be competitive with homogeneous loss pathways, especially in dusty urban and desertified environments.

Description: Heterogeneous processes on dust particles are important for understanding the chemistry and radiative balance of the atmosphere. This paper investigates an intense Asian dust storm episode observed at Mount Heng (1269 m a.s.l.) in southern China on 24–26 April 2009. A set of aerosol and trace gas data collected during the study was analyzed to investigate their chemical evolution and heterogeneous photochemistry as the dust traveled to southern China. Results show that the mineral dust arriving at Mt. Heng experienced significant modifications during transport, with large enrichments in secondary species (sulfate, nitrate, and ammonium) compared with the dust composition collected at an upwind mountain top site (Mount Hua). A photochemical age "clock" (−Log10(NOx/NOy)) was employed to quantify the atmospheric processing time. The result indicates an obvious increase in the abundance of secondary water-soluble ions in dust particles with the air mass atmospheric processing time. Based on the observations, a 4-stage evolution process is proposed for carbonate-containing Asian dust, starting from fresh dust to particles coated with hydrophilic and acidic materials. Daytime-enhanced nitrite formation on the dust particles was also observed, which indicates the recent laboratory result of the TiO2 photocatalysis of NO2 as a potential source of nitrite and nitrous acid.

Description: The North China plain is a region with megacities and huge populations. Aerosols over the highly polluted area have a significant impact on the regional and global climate. In order to investigate the physical and chemical characteristics of aerosol particles in elevated layers there, observations were carried out at the summit of Mt. Tai (1534 m a.s.l.) from 19 to 28 April, 2010, when the air masses were advected from the east (phase-I: 19–21 April), from the south (phase-II: 22–25 April), and from the northwest (phase-III: 26–28 April). Individual aerosol particles were identified with transmission electron microscopy (TEM), new particle formation (NPF) and growth events were monitored by a wide-range particle spectrometer, and ion concentrations in PM2.5 were analyzed. During phase-I and phase-II, haze layers caused by anthropogenic pollution were observed, and a high percentage of particles were sulfur-rich (47–49%). In phase-III, the haze disappeared due to the intrusion of cold air from the northwest, and mineral dust particles from deserts were dominant (43%). NPF followed by particle growth during daytime was more pronounced on hazy than on clear days. Particle growth during daytime resulted in an increase of particle geometric mean diameter from 10–22 nm in the morning to 56–96 nm in the evening. TEM analysis suggests that sulfuric acid and secondary organic compounds should be important factors for particle nucleation and growth. However, the presence of fine anthropogenic particles (e.g., soot, metal, and fly ash) embedded within S-rich particles indicates that they could weaken NPF and enhance particle growth through condensation and coagulation. Abundant mineral particles in phase-III likely suppressed the NPF processes because they supplied sufficient area on which acidic gases or acids condensed.