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Open AccessJournal ArticleDOI

Atmospheric composition change – global and regional air quality

Paul S. Monks, +68 more
- 01 Oct 2009 - 
- Vol. 43, Iss: 33, pp 5268-5350
TLDR
A review of the state of scientific understanding in relation to global and regional air quality is outlined in this article, in terms of emissions, processing and transport of trace gases and aerosols.
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This article is published in Atmospheric Environment.The article was published on 2009-10-01 and is currently open access. It has received 760 citations till now. The article focuses on the topics: Air quality index.

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Citations
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An inventory of gaseous and primary aerosol emissions in Asia in the year 2000 : NASA global tropospheric experiment transport and chemical evolution over the pacific (TRACE-P): Measurements and analysis (TRACEP1)

TL;DR: In this paper, an inventory of air pollutant emissions in Asia in the year 2000 is developed to support atmospheric modeling and analysis of observations taken during the TRACE-P experiment funded by the National Aeronautics and Space Administration (NASA) and the ACE-Asia experiment, in which emissions are estimated for all major anthropogenic sources, including biomass burning, in 64 regions of Asia.

Secondary Organic Aerosol Formation from Anthropogenic Air Pollution: Rapid and Higher than Expected

TL;DR: This paper showed that reactive anthropogenic VOCs (AVOCs) produce much larger amounts of SOA than these models predict, even shortly after sunrise, and a significant fraction of the excess SOA is formed from first-generation AVOC oxidation products.
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Mountain Weather and Climate

TL;DR: In this paper, the authors present a review of mountain bioclimatology and changes in mountain climates, and discuss the role of orography in the evolution of mountain climate.
References
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Journal ArticleDOI

A model investigation of tropospheric ozone chemical tendencies in long-range transported pollution plumes

Abstract: The impact of continental outflow on the ozone chemical tendencies (i.e., production and loss rates) is quantified in the North Atlantic and northwest Pacific regions using the GEOS-Chem and the MOZECH global models of chemistry and transport. The ozone tendencies simulated by these global models are compared to box model simulations constrained by observations in different regions and seasons. The two global models generally capture the seasonal and regional variations of the ozone tendencies. The largest discrepancies between the ozone tendencies from the box model and those from the global models are found in the lower troposphere of the eastern North Atlantic during the ACSOE campaign and are attributed to differences between chemical schemes and too strong NO x concentrations in the global models. The background and plume (i.e., impacted by continental outflow) environments are differentiated over the oceanic areas using criteria based on simulated daily mean CO concentrations. The ozone tendencies in the plume environment differ from that in the background over the entire column in North Atlantic and northwest Pacific at all seasons. According to the models, net ozone production is enhanced by 2 to 6 ppbv/day in the boundary layer and by 1 to 3 ppbv/day in the upper troposphere, whereas the effect of pollution ranges from −1 ppbv/day to +1 ppbv/day in the middle troposphere (3–7 km), depending on the model used. The different responses of the two models are determined by differences in the water vapor distributions relative to those of pollutants in the plumes. In particular, GEOS-Chem tends to transport pollution in a drier sector of cyclones than MOZECH.
Journal ArticleDOI

Relative tropospheric photolysis rates of HCHO and HCDO measured at the European Photoreactor Facility.

TL;DR: The atmospheric implications of the large isotope effect in the relative rate of photolysis and quantum yield of the formaldehyde isotopologues are discussed in relation to the global hydrogen budget.
Journal ArticleDOI

Long-range transport of tropospheric ozone

TL;DR: In this article, models of ozone and other oxidants are suggested for episodes where air masses of continental origin reach the British Isles during fair weather in summer, and it is shown that ozone stays at high levels for several days, allowing for transport over long distances (∼ 1,000 km).
Journal ArticleDOI

Modeling New Particle Formation During Air Pollution Episodes: Impacts on Aerosol and Cloud Condensation Nuclei

TL;DR: In this article, the impact of new particle formation on regional air quality and CCN formation is explored using the UAM-AERO air quality model, where new particles are formed by ternary nucleation of sulfuric acid, ammonia and water.
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Frequently Asked Questions (12)
Q1. What are the contributions mentioned in the paper "Atmospheric composition change - global and regional air quality" ?

In this review the state of scientific understanding in relation to global and regional air quality is outlined. Trends in anthropogenic emissions both by region and globally are discussed as well as biomass burning emissions. New findings with respect to the transport of pollutants across the scales are discussed, in particular the move to quantify the impact of long-range transport on regional air quality. In particular, the policy challenges for concerted air quality and climate change policy ( co-benefit ) are discussed. 

Fossil fuel extraction and burning, energy production and consumption, industrial activities, transportation and landfills have also led to the emissions of large quantities of pollutants into the atmosphere. 

A step forward in deriving parameterizations of topographic venting for larger scale models is the quantification of the air mass exchanged vertically on a sub-grid scale. 

Particular areas where understanding is lacking include uncertainties in the mechanisms of the initial oxidation sequences to first generation products, and limitations in the available information on the subsequent chemistry of many of the classes of product known tobe generated. 

the main challenges in the estimation of uncertainties in emissions are related to the uncertainties in input data and in the development of methods for quantifying systematic errors. 

By overlaying the distribution of frequency of occurrence with land use changes, the amount of anthropogenic dust emissions can be evaluated. 

Over the last three decades, fire emissions estimates have developed from early inventories based on average fire return times and biomass estimates to detailed studies based on satellite data and sophisticated modelling predicting emissions with high spatial and temporal resolution. 

Uncertainty in emission scenario analysis at urban scale has also been tackled using Bayesian Monte-Carlo techniques (Deguillaume et al., 2008). 

The degradation of aromatic hydrocarbons, although usually only initiated significantly by reaction with OH, can proceed via a number of different routes to generate a large variety of structurally complex ring-retained and ring-opened products e.g. 

As dust has some unique spectral signatures (Dubovik et al., 2002), it is possible to separate pixels with freshly emitted dust from other aerosols. 

Technical challenges are also linked to fast hygroscopicity measurements for airborne applications in order to document high altitude hygroscopicity. 

Other questions also remain open, such as whether the concentrated emissions of gases, aerosols and aerosol precursors in the megacities have a substantial impact on regional and global climate.