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		<title>Atmosphere</title>
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        <item rdf:about="http://www.mdpi.com/2073-4433/4/2/157">
	<title><![CDATA[Atmosphere, Vol. 4, Pages 157-168: Spatial and Temporal Variations of Atmospheric Aerosol in Osaka]]></title>
	<link>http://www.mdpi.com/2073-4433/4/2/157</link>
	<description>It is well known that the aerosol distribution in Asia is complex due to both the increasing emissions of the anthropogenic aerosols associated with economic growth and the behavior of natural dusts. Therefore, detailed observations of atmospheric particles in Asian urban cities are important. In this work, we focus on the spatial and temporal variations of atmospheric particles around Higashi-Osaka in Japan. Higashi-Osaka is located in the eastern part of Osaka, the second-largest city in Japan, and is famous for small- and medium-sized manufacturing enterprises. For this study, we placed various ground measurement devices around the Higashi-Osaka campus of Kinki University including a Cimel sunphotometer supported by NASA/AERONET (Aerosol robotics network), suspended particulate matter (SPM) sampler and LIDAR (light detection and ranging). Individual particle analyses with a SEM (scanning electron microscope)/EDX (energy-dispersive X-ray analyzer) show the temporal variations of particle properties, such as size, shape and components, during a dust event on 21 March 2010. The simultaneous measurement using a portable sun photometer with AERONET was conducted from April to November 2011. A comparison of the data at each site and the combination of the observed LIDAR data and model simulations indicate the difference in the transportation processes between dust and anthropogenic particles. We suppose this difference is attributed to the differences in the vertical aerosol profiles, where one aerosol is transported over Mount Ikoma and the other is blocked by it.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2013-05-21</prism:publicationDate>
	<prism:volume>4</prism:volume>
	<prism:number>2</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos4020157</prism:doi>
	<prism:startingPage>157</prism:startingPage>
		<prism:endingPage>168</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Spatial and Temporal Variations of Atmospheric Aerosol in Osaka]]></dc:title>
    <dc:date>2013-05-21</dc:date>
	<dc:identifier>doi: 10.3390/atmos4020157</dc:identifier>
    	<dc:creator>Makiko Nakata</dc:creator>
		<dc:creator>Itaru Sano</dc:creator>
		<dc:creator>Sonoyo Mukai</dc:creator>
		<dc:creator>Brent Holben</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/4/2/132">
	<title><![CDATA[Atmosphere, Vol. 4, Pages 132-156: Numerical Modeling of Climate-Chemistry Connections: Recent Developments and Future Challenges]]></title>
	<link>http://www.mdpi.com/2073-4433/4/2/132</link>
	<description>This paper reviews the current state and development of different numerical model classes that are used to simulate the global atmospheric system, particularly Earth’s climate and climate-chemistry connections. The focus is on Chemistry-Climate Models. In general, these serve to examine dynamical and chemical processes in the Earth atmosphere, their feedback, and interaction with climate. Such models have been established as helpful tools in addition to analyses of observational data. Definitions of the global model classes are given and their capabilities as well as weaknesses are discussed. Examples of scientific studies indicate how numerical exercises contribute to an improved understanding of atmospheric behavior. There, the focus is on synergistic investigations combining observations and model results. The possible future developments and challenges are presented, not only from the scientific point of view but also regarding the computer technology and respective consequences for numerical modeling of atmospheric processes. In the future, a stronger cross-linkage of subject-specific scientists is necessary, to tackle the looming challenges. It should link the specialist discipline and applied computer science.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2013-05-17</prism:publicationDate>
	<prism:volume>4</prism:volume>
	<prism:number>2</prism:number>
	<prism:section>Review</prism:section>
	<prism:doi>10.3390/atmos4020132</prism:doi>
	<prism:startingPage>132</prism:startingPage>
		<prism:endingPage>156</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Numerical Modeling of Climate-Chemistry Connections: Recent Developments and Future Challenges]]></dc:title>
    <dc:date>2013-05-17</dc:date>
	<dc:identifier>doi: 10.3390/atmos4020132</dc:identifier>
    	<dc:creator>Martin Dameris</dc:creator>
		<dc:creator>Patrick Jöckel</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/4/2/113">
	<title><![CDATA[Atmosphere, Vol. 4, Pages 113-131: Decreases in Mercury Wet Deposition over the United States during 2004–2010: Roles of Domestic and Global Background Emission Reductions]]></title>
	<link>http://www.mdpi.com/2073-4433/4/2/113</link>
	<description>Wet deposition of mercury (Hg) across the United States is influenced by changes in atmospheric conditions, domestic emissions and global background emissions. We examine trends in Hg precipitation concentrations at 47 Mercury Deposition Network (MDN) sites during 2004–2010 by using the GEOS-Chem nested-grid Hg simulation. We run the model with constant anthropogenic emissions and subtract the model results from the observations. This helps to remove the variability in observed Hg concentrations caused by meteorological factors, including precipitation. We find significant decreasing trends in Hg concentrations in precipitation at MDN sites in the Northeast (−4.1 ± 0.49% yr−1) and Midwest (−2.7 ± 0.68% yr−1). Over the Southeast (−0.53 ± 0.59% yr−1), trends are weaker and not significant, while over the West, trends are highly variable. We conduct model simulations assuming a 45% decrease in Hg emissions from domestic sources in the modeled period and a uniform 12% decrease in background atmospheric Hg concentrations. The combination of domestic emission reductions and decreasing background concentrations explains the observed trends over the Northeast and Midwest, with domestic emission reductions accounting for 58–46% of the decreasing trends. Over the Southeast, we overestimate the observed decreasing trend, indicating potential issues with our assumption of uniformly decreasing background Hg concentrations.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2013-05-10</prism:publicationDate>
	<prism:volume>4</prism:volume>
	<prism:number>2</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos4020113</prism:doi>
	<prism:startingPage>113</prism:startingPage>
		<prism:endingPage>131</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Decreases in Mercury Wet Deposition over the United States during 2004–2010: Roles of Domestic and Global Background Emission Reductions]]></dc:title>
    <dc:date>2013-05-10</dc:date>
	<dc:identifier>doi: 10.3390/atmos4020113</dc:identifier>
    	<dc:creator>Yanxu Zhang</dc:creator>
		<dc:creator>Lyatt Jaeglé</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/4/2/94">
	<title><![CDATA[Atmosphere, Vol. 4, Pages 94-112: Spatio-Temporal Analysis of Droughts in Semi-Arid Regions by Using Meteorological Drought Indices]]></title>
	<link>http://www.mdpi.com/2073-4433/4/2/94</link>
	<description>Six meteorological drought indices including percent of normal (PN), standardized precipitation index (SPI), China-Z index (CZI), modified CZI (MCZI),  Z-Score (Z), the aridity index of E. de Martonne (I) are compared and evaluated for assessing spatio-temporal dynamics of droughts in six climatic regions in Iran. Results indicated that by consideration of the advantages and disadvantages of the mentioned drought predictors in Iran, the Z-Score, CZI and MCZI could be used as a good meteorological drought predictor. Depending on the month, the length of drought and climatic conditions of the region, they are an alternative to the SPI that has limitations both because of only a few available long term data series in Iran and its complex structure.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2013-04-25</prism:publicationDate>
	<prism:volume>4</prism:volume>
	<prism:number>2</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos4020094</prism:doi>
	<prism:startingPage>94</prism:startingPage>
		<prism:endingPage>112</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Spatio-Temporal Analysis of Droughts in Semi-Arid Regions by Using Meteorological Drought Indices]]></dc:title>
    <dc:date>2013-04-25</dc:date>
	<dc:identifier>doi: 10.3390/atmos4020094</dc:identifier>
    	<dc:creator>Alireza Shahabfar</dc:creator>
		<dc:creator>Josef Eitzinger</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/4/2/72">
	<title><![CDATA[Atmosphere, Vol. 4, Pages 72-93: Observation and Analysis of Particle Nucleation at a Forest Site in Southeastern US]]></title>
	<link>http://www.mdpi.com/2073-4433/4/2/72</link>
	<description>This study examines the characteristics of new particle formation at a forest site in southeastern US. Particle size distributions above a Loblolly pine plantation were measured between November 2005 and September 2007 and analyzed by event type and frequency, as well as in relation to meteorological and atmospheric chemical conditions. Nucleation events occurred on 69% of classifiable observation days. Nucleation frequency was highest in spring. The highest daily nucleation (class A and B events) frequency  (81%) was observed in April. The average total particle number concentration on nucleation days was 8,684 cm−3 (10 &amp;amp;lt; Dp &amp;amp;lt; 250 nm) and 3,991 cm−3 (10 &amp;amp;lt; Dp &amp;amp;lt; 25 nm) with a mode diameter of 28 nm with corresponding values on non-nucleation days of  2,143 cm−3, 655 cm−3, and 44.5 nm, respectively. The annual average growth rate during nucleation events was 2.7 ± 0.3 nm·h−1. Higher growth rates were observed during summer months with highest rates observed in May (5.0 ± 3.6 nm·h−1). Winter months were associated with lower growth rates, the lowest occurring in February (1.2 ± 2.2 nm·h−1). Consistent with other studies, nucleation events were more likely to occur on days with higher radiative flux and lower relative humidity compared to non-nucleation days. The daily minimum in the condensation sink, which typically occurred 2 to 3 h after sunrise, was a good indicator of the timing of nucleation onset. The intensity of the event, indicated by the total particle number concentration, was well correlated with photo-synthetically active radiation, used here as a surrogate for total global radiation, and relative humidity. Even though the role of biogenic VOC in the initial nuclei formation is not understood from this study, the relationships with chemical precursors and secondary aerosol products associated with nucleation, coupled with diurnal boundary layer dynamics and seasonal meteorological patterns, suggest that H2SO4 and biogenic VOC play a role in nucleated particle growth at this site.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2013-04-03</prism:publicationDate>
	<prism:volume>4</prism:volume>
	<prism:number>2</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos4020072</prism:doi>
	<prism:startingPage>72</prism:startingPage>
		<prism:endingPage>93</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Observation and Analysis of Particle Nucleation at a Forest Site in Southeastern US]]></dc:title>
    <dc:date>2013-04-03</dc:date>
	<dc:identifier>doi: 10.3390/atmos4020072</dc:identifier>
    	<dc:creator>Priya Pillai</dc:creator>
		<dc:creator>Andrey Khlystov</dc:creator>
		<dc:creator>John Walker</dc:creator>
		<dc:creator>Viney Aneja</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/4/1/48">
	<title><![CDATA[Atmosphere, Vol. 4, Pages 48-71: Characterizing a New Surface-Based Shortwave Cloud Retrieval Technique, Based on Transmitted Radiance for Soil and Vegetated Surface Types]]></title>
	<link>http://www.mdpi.com/2073-4433/4/1/48</link>
	<description>This paper presents an approach using the GEneralized Nonlinear Retrieval Analysis (GENRA) tool and general inverse theory diagnostics including the maximum likelihood solution and the Shannon information content to investigate the performance of a new spectral technique for the retrieval of cloud optical properties from surface based transmittance measurements. The cumulative retrieval information over broad ranges in cloud optical thickness (τ), droplet effective radius (re), and overhead sun angles is quantified under two conditions known to impact transmitted radiation; the variability in land surface albedo and atmospheric water vapor content. Our conclusions are: (1) the retrieved cloud properties are more sensitive to the natural variability in land surface albedo than to water vapor content; (2) the new spectral technique is more accurate (but still imprecise) than a standard approach, in particular for τ between 5 and 60 and re less than approximately 20 μm; and (3) the retrieved cloud properties are dependent on sun angle for clouds of  from 5 to 10 and re &amp;amp;lt; 10 μm, with maximum sensitivity obtained for an overhead sun.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2013-03-19</prism:publicationDate>
	<prism:volume>4</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos4010048</prism:doi>
	<prism:startingPage>48</prism:startingPage>
		<prism:endingPage>71</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Characterizing a New Surface-Based Shortwave Cloud Retrieval Technique, Based on Transmitted Radiance for Soil and Vegetated Surface Types]]></dc:title>
    <dc:date>2013-03-19</dc:date>
	<dc:identifier>doi: 10.3390/atmos4010048</dc:identifier>
    	<dc:creator>Odele Coddington</dc:creator>
		<dc:creator>Peter Pilewskie</dc:creator>
		<dc:creator>K. Schmidt</dc:creator>
		<dc:creator>Patrick McBride</dc:creator>
		<dc:creator>Tomislava Vukicevic</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/4/1/35">
	<title><![CDATA[Atmosphere, Vol. 4, Pages 35-47: Dust Detection and Optical Depth Retrieval Using MSG‑SEVIRI Data]]></title>
	<link>http://www.mdpi.com/2073-4433/4/1/35</link>
	<description>Thanks to its observational frequency of 15 min, the Meteosat Second Generation (MSG) geostationary satellite offers a great potential to monitor dust storms. To explore this potential, an algorithm for the detection and the retrieval of dust aerosol optical properties has been tested. This is a multispectral algorithm based on visible and infrared data which has been applied to 15 case studies selected between 2007 and 2011. The algorithm has been validated in the latitude–longitude box between 30 and 50 degrees north, and −10 and 20 degrees east, respectively. Hereafter we present the obtained results that have been validated against Aerosol Robotic Network (AERONET) ground-based measurements and compared with the retrievals from the Moderate Resolution Imaging Spectroradiometer (MODIS) on NASA’s Terra and Aqua satellites. The dust aerosol optical depth variations observed at the AERONET sites are well reproduced, showing good correlation of about 0.77, and a root mean square difference within 0.08, and the spatial patterns retrieved by using the algorithm developed are in agreement with those observed by MODIS.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2013-03-05</prism:publicationDate>
	<prism:volume>4</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos4010035</prism:doi>
	<prism:startingPage>35</prism:startingPage>
		<prism:endingPage>47</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Dust Detection and Optical Depth Retrieval Using MSG‑SEVIRI Data]]></dc:title>
    <dc:date>2013-03-05</dc:date>
	<dc:identifier>doi: 10.3390/atmos4010035</dc:identifier>
    	<dc:creator>Filomena Romano</dc:creator>
		<dc:creator>Elisabetta Ricciardelli</dc:creator>
		<dc:creator>Domenico Cimini</dc:creator>
		<dc:creator>Francesco Di Paola</dc:creator>
		<dc:creator>Mariassunta Viggiano</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/4/1/17">
	<title><![CDATA[Atmosphere, Vol. 4, Pages 17-34: Biomass Burning Aerosols Observed in Northern Finland during the 2010 Wildfires in Russia]]></title>
	<link>http://www.mdpi.com/2073-4433/4/1/17</link>
	<description>A smoke plume originating from the massive wildfires near Moscow was clearly detected in northern Finland on 30 July 2010. Measurements made with remote sensing instruments demonstrated how the biomass burning aerosols affected the chemical and optical characteristics of the atmosphere in regions hundreds of kilometers away from the actual fires. In this study, we used MODIS, AIRS, CALIOP, PFR, ceilometers, FTS and Brewer data to quantify the properties of the transported smoke plume. In addition, in situ measurements of aerosol concentration (DMPS), absorption (aethalometer) and scattering (nephelometer) are presented. We found that due to the smoke plume in northern Finland, the daily averaged optical thickness of aerosols increased fourfold, and MODIS retrieved AOD as high as 4.5 for the thickest part of the plume. FTS measurements showed that CO concentration increased by 100% during the plume. CALIOP and ceilometer measurements revealed that the smoke plume was located close to the surface, below 3 km, and that the plume was not homogeneously mixed. In addition, in situ measurements showed that the scattering and absorption coefficients were almost 20 times larger in the smoke plume than on average, and that the number of particles larger than 320 nm increased 14-fold. Moreover, a comparison with in situ measurements recorded in eastern Finland on the previous day showed that the transport from eastern to northern Finland decreased the scattering coefficient, black carbon concentration, and total number concentration 0.5%/h, 1.5%/h and 2.0%/h, respectively.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2013-02-28</prism:publicationDate>
	<prism:volume>4</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos4010017</prism:doi>
	<prism:startingPage>17</prism:startingPage>
		<prism:endingPage>34</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Biomass Burning Aerosols Observed in Northern Finland during the 2010 Wildfires in Russia]]></dc:title>
    <dc:date>2013-02-28</dc:date>
	<dc:identifier>doi: 10.3390/atmos4010017</dc:identifier>
    	<dc:creator>Tero Mielonen</dc:creator>
		<dc:creator>Veijo Aaltonen</dc:creator>
		<dc:creator>Heikki Lihavainen</dc:creator>
		<dc:creator>Antti-Pekka Hyvärinen</dc:creator>
		<dc:creator>Antti Arola</dc:creator>
		<dc:creator>Mika Komppula</dc:creator>
		<dc:creator>Rigel Kivi</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/4/1/1">
	<title><![CDATA[Atmosphere, Vol. 4, Pages 1-16: A Comparison of the Mineral Dust Absorptive Properties between Two Asian Dust Events]]></title>
	<link>http://www.mdpi.com/2073-4433/4/1/1</link>
	<description>Asian dust events are generated by deep convection from strong low pressure systems that form over mineral dust source regions. This study compares the mineral dust optical properties of two strong Asian dust events from the winter (December 2007) and spring (March 2010) seasons using AERONET retrieved parameters from three sites along the dust event path: SACOL (dust source region), Xianghe (downwind mixed aerosol region), and Taihu (downwind pollution region). The parameters include: aerosol effective radius, optical depth (t), absorptive optical depth (tabs), their respective wavelength dependences or Angstrom exponents (a and aabs), and the spectral single scattering albedo (wo(λ)). The a440–870 values in both cases do not exceed 0.62 indicating coarse mode particle dominance at all three sites. The winter case is shown to have carbonaceous influences at all three sites as given by aabs440–870 between 1.3 and 1.8 with strong spectral tabs absorption. The spring case is more dust dominant with aabs440–870 of 1.7–2.5 (noting that the largest value occurred at Taihu) with strong tabs absorption primarily in the visible wavelengths. Comparison studies between the observed and theoretically calculated wo(λ) for the winter and spring cases have shown an excellent agreement except for the winter case at Taihu due to pollution influences. The comparison studies also suggest that wo(λ) is more sensitive to particle absorptive properties rather than particle size. The sharp increase in the aerosol radiative effect (ARE) during the dust events with AREBOA &amp;amp;gt; ARETOA suggests a stronger aerosol cooling effect at the surface than at the TOA.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2013-01-28</prism:publicationDate>
	<prism:volume>4</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos4010001</prism:doi>
	<prism:startingPage>1</prism:startingPage>
		<prism:endingPage>16</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[A Comparison of the Mineral Dust Absorptive Properties between Two Asian Dust Events]]></dc:title>
    <dc:date>2013-01-28</dc:date>
	<dc:identifier>doi: 10.3390/atmos4010001</dc:identifier>
    	<dc:creator>Timothy Logan</dc:creator>
		<dc:creator>Baike Xi</dc:creator>
		<dc:creator>Xiquan Dong</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/3/4/591">
	<title><![CDATA[Atmosphere, Vol. 3, Pages 591-619: Exploration of a Polarized Surface Bidirectional Reflectance Model Using the Ground-Based Multiangle SpectroPolarimetric Imager]]></title>
	<link>http://www.mdpi.com/2073-4433/3/4/591</link>
	<description>Accurate characterization of surface reflection is essential for retrieval of aerosols using downward-looking remote sensors. In this paper, observations from the Ground-based Multiangle SpectroPolarimetric Imager (GroundMSPI) are used to evaluate a surface polarized bidirectional reflectance distribution function (PBRDF) model. GroundMSPI is an eight-band spectropolarimetric camera mounted on a rotating gimbal to acquire pushbroom imagery of outdoor landscapes. The camera uses a very accurate photoelastic-modulator-based polarimetric imaging technique to acquire Stokes vector measurements in three of the instrument’s bands (470, 660, and 865 nm). A description of the instrument is presented, and observations of selected targets within a scene acquired on 6 January 2010 are analyzed. Data collected during the course of the day as the Sun moved across the sky provided a range of illumination geometries that facilitated evaluation of the surface model, which is comprised of a volumetric reflection term represented by the modified Rahman-Pinty-Verstraete function plus a specular reflection term generated by a randomly oriented array of Fresnel-reflecting microfacets. While the model is fairly successful in predicting the polarized reflection from two grass targets in the scene, it does a poorer job for two manmade targets (a parking lot and a truck roof), possibly due to their greater degree of geometric organization. Several empirical adjustments to the model are explored and lead to improved fits to the data. For all targets, the data support the notion of spectral invariance in the angular shape of the unpolarized and polarized surface reflection. As noted by others, this behavior provides valuable constraints on the aerosol retrieval problem, and highlights the importance of multiangle observations.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2012-12-18</prism:publicationDate>
	<prism:volume>3</prism:volume>
	<prism:number>4</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos3040591</prism:doi>
	<prism:startingPage>591</prism:startingPage>
		<prism:endingPage>619</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Exploration of a Polarized Surface Bidirectional Reflectance Model Using the Ground-Based Multiangle SpectroPolarimetric Imager]]></dc:title>
    <dc:date>2012-12-18</dc:date>
	<dc:identifier>doi: 10.3390/atmos3040591</dc:identifier>
    	<dc:creator>David Diner</dc:creator>
		<dc:creator>Feng Xu</dc:creator>
		<dc:creator>John Martonchik</dc:creator>
		<dc:creator>Brian Rheingans</dc:creator>
		<dc:creator>Sven Geier</dc:creator>
		<dc:creator>Veljko Jovanovic</dc:creator>
		<dc:creator>Ab Davis</dc:creator>
		<dc:creator>Russell Chipman</dc:creator>
		<dc:creator>Stephen McClain</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/3/4/573">
	<title><![CDATA[Atmosphere, Vol. 3, Pages 573-590: Continuous Cropping and Moist Deep Convection on the Canadian Prairies]]></title>
	<link>http://www.mdpi.com/2073-4433/3/4/573</link>
	<description>Summerfallow is cropland that is purposely kept out of production during a growing season to conserve soil moisture. On the Canadian Prairies, a trend to continuous cropping with a reduction in summerfallow began after the summerfallow area peaked in 1976. This study examined the impact of this land-use change on convective available potential energy (CAPE), a necessary but not sufficient condition for moist deep convection. All else being equal, an increase in CAPE increases the probability-of-occurrence of convective clouds and their intensity if they occur. Representative Bowen ratios for the Black, Dark Brown, and Brown soil zones were determined for 1976: the maximum summerfallow year, 2001: our baseline year, and 20xx: a hypothetical year with the maximum-possible annual crop area. Average mid-growing-season Bowen ratios and noon solar radiation were used to estimate the reduction in the lifted index (LI) from land-use weighted evapotranspiration in each study year. LI is an index of CAPE, and a reduction in LI indicates an increase in CAPE. The largest reductions in LI were found for the Black soil zone. They were −1.61 ± 0.18, −1.77 ± 0.14 and −1.89 ± 0.16 in 1976, 2001 and 20xx, respectively. These results suggest that, all else being equal, the probability-of-occurrence of moist deep convection in the Black soil zone was lower in 1976 than in the base year 2001, and it will be higher in 20xx when the annual crop area reaches a maximum. The trend to continuous cropping had less impact in the drier Dark Brown and Brown soil zones.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2012-12-13</prism:publicationDate>
	<prism:volume>3</prism:volume>
	<prism:number>4</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos3040573</prism:doi>
	<prism:startingPage>573</prism:startingPage>
		<prism:endingPage>590</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Continuous Cropping and Moist Deep Convection on the Canadian Prairies]]></dc:title>
    <dc:date>2012-12-13</dc:date>
	<dc:identifier>doi: 10.3390/atmos3040573</dc:identifier>
    	<dc:creator>Bharat Shrestha</dc:creator>
		<dc:creator>Richard Raddatz</dc:creator>
		<dc:creator>Raymond Desjardins</dc:creator>
		<dc:creator>Devon Worth</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/3/4/557">
	<title><![CDATA[Atmosphere, Vol. 3, Pages 557-572: A Comprehensive Modeling Study on Regional Climate Model (RCM) Application — Regional Warming Projections in Monthly Resolutions under IPCC A1B Scenario]]></title>
	<link>http://www.mdpi.com/2073-4433/3/4/557</link>
	<description>Some of the major dimensions of climate change include increase in surface temperature, longer spells of droughts in significant portions of the world, associated higher evapotranspiration rates, and so on. It is therefore essential to comprehend the future possible scenario of climate change in terms of global warming. A high resolution limited area Regional Climate Model (RCM) can produce reasonably appropriate projections to be used for climate-scenario generation in country-scale. This paper features the development of future surface temperature projections for Bangladesh on monthly resolution for each year from 2011 to 2100 applying Providing Regional Climates for Impacts Studies (PRECIS), and it explains in detail the modeling processes including the model features, domain size selection, bias identification as well as construction of change field for the concerned climatic variable, in this case, surface temperature. PRECIS was run on a 50 km horizontal grid-spacing under the Intergovernmental Panel on Climate Change (IPCC) A1B scenario and it was found to perform reasonably well in simulating future surface temperature of Bangladesh. The linear regression between observed and model simulated results of monthly average temperatures, within the 30-year period from 1971 to 2000, gives a high correlation of 0.93. The applied change field in average annual temperature shows only 0.5 °C–1 °C deviation from the observed values over the period from 2005 to 2008. Eventually, from the projected average temperature change during the years 1971–2000, it is apparent that warming in Bangladesh prevails invariably every month, which might eventually result in an average annual increase of 4 °C by the year 2100. Calculated anomalies in country-average annual temperature mostly remain on the positive side throughout the period of 2071–2100 indicating an overall up-shift. Apart from these quantitative analyses of temporal changes of temperature, this paper also illustrates their spatial distribution with a view to identify the most vulnerable zones under consequent warming through future times.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2012-10-31</prism:publicationDate>
	<prism:volume>3</prism:volume>
	<prism:number>4</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos3040557</prism:doi>
	<prism:startingPage>557</prism:startingPage>
		<prism:endingPage>572</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[A Comprehensive Modeling Study on Regional Climate Model (RCM) Application — Regional Warming Projections in Monthly Resolutions under IPCC A1B Scenario]]></dc:title>
    <dc:date>2012-10-31</dc:date>
	<dc:identifier>doi: 10.3390/atmos3040557</dc:identifier>
    	<dc:creator>Mohammad Rajib</dc:creator>
		<dc:creator>Md. Rahman</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/3/4/537">
	<title><![CDATA[Atmosphere, Vol. 3, Pages 537-556: Modelling Regional Surface Energy Exchange and Boundary Layer Development in Boreal Sweden — Comparison of Mesoscale Model (RAMS) Simulations with Aircraft and Tower Observations]]></title>
	<link>http://www.mdpi.com/2073-4433/3/4/537</link>
	<description>Simulation of atmospheric and surface processes with an atmospheric model (RAMS) during a period of ten days in August 2001 over a boreal area in Sweden were compared to tower measurements and aircraft measurements of vertical profiles as well as surface fluxes from low altitude flights. The shape of the vertical profiles was simulated reasonably well by the model although there were significant biases in absolute values. Surface fluxes were less well simulated and the model showed considerable sensitivity to initial soil moisture conditions. The simulations were performed using two different land cover databases, the original one supplied with the RAMS model and the more detailed CORINE database. The two different land cover data bases resulted in relatively large fine scale differences in the simulated values. The conclusion of this study is that RAMS has the potential to be used as a tool to estimate boundary layer conditions and surface fluxes and meteorology over a boreal area but also that further improvement is needed.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2012-10-30</prism:publicationDate>
	<prism:volume>3</prism:volume>
	<prism:number>4</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos3040537</prism:doi>
	<prism:startingPage>537</prism:startingPage>
		<prism:endingPage>556</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Modelling Regional Surface Energy Exchange and Boundary Layer Development in Boreal Sweden — Comparison of Mesoscale Model (RAMS) Simulations with Aircraft and Tower Observations]]></dc:title>
    <dc:date>2012-10-30</dc:date>
	<dc:identifier>doi: 10.3390/atmos3040537</dc:identifier>
    	<dc:creator>Elena Kvon</dc:creator>
		<dc:creator>Janno Tuulik</dc:creator>
		<dc:creator>Meelis Mölder</dc:creator>
		<dc:creator>Anders Lindroth</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/3/4/522">
	<title><![CDATA[Atmosphere, Vol. 3, Pages 522-536: Low-Frequency Rotation of Surface Winds over Canada]]></title>
	<link>http://www.mdpi.com/2073-4433/3/4/522</link>
	<description>Hourly surface observations from the Canadian Weather Energy and Engineering Dataset were analyzed with respect to long-term wind direction drift or rotation. Most of the Canadian landmass, including the High Arctic, exhibits a spatially consistent and remarkably steady anticyclonic rotation of wind direction. The period of anticyclonic rotation recorded at 144 out of 149 Canadian meteostations directly correlated with latitude and ranged from 7 days at Medicine Hat (50°N, 110°W) to 25 days at Resolute (75°N, 95°W). Only five locations in the vicinity of the Rocky Mountains and Pacific Coast were found to obey a “negative” (i.e., cyclonic) rotation. The observed anticyclonic rotation appears to be a deterministic, virtually ubiquitous, and highly persistent feature of continental surface wind. These findings are directly applicable to probabilistic assessments of airborne pollutants.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2012-10-25</prism:publicationDate>
	<prism:volume>3</prism:volume>
	<prism:number>4</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos3040522</prism:doi>
	<prism:startingPage>522</prism:startingPage>
		<prism:endingPage>536</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Low-Frequency Rotation of Surface Winds over Canada]]></dc:title>
    <dc:date>2012-10-25</dc:date>
	<dc:identifier>doi: 10.3390/atmos3040522</dc:identifier>
    	<dc:creator>Vladimir Korolevych</dc:creator>
		<dc:creator>Richard Richardson</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/3/4/495">
	<title><![CDATA[Atmosphere, Vol. 3, Pages 495-521: Initial Assessment of the Spectrometer for Sky-Scanning, Sun-Tracking Atmospheric Research (4STAR)-Based Aerosol Retrieval: Sensitivity Study]]></title>
	<link>http://www.mdpi.com/2073-4433/3/4/495</link>
	<description>The Spectrometer for Sky-Scanning, Sun-Tracking Atmospheric Research (4STAR) being developed for airborne measurements will offer retrievals of aerosol microphysical and optical properties from multi-angular and multi-spectral measurements of sky radiance and direct-beam sun transmittance. In this study, we assess the expected accuracy of the 4STAR-based aerosol retrieval and its sensitivity to major sources of anticipated perturbations in the 4STAR measurements. The major anticipated perturbations are (1) an apparent enhancement of sky radiance at small scattering angles associated with the necessarily compact design of the 4STAR and (2) an offset (i.e., uncertainty) of sky radiance calibration independent of scattering angle. The assessment is performed through application of the operational AERONET aerosol retrieval and constructed synthetic 4STAR-like data. Particular attention is given to the impact of these perturbations on the broadband fluxes and the direct aerosol radiative forcing. The results from this study suggest that limitations in the accuracy of 4STAR-retrieved particle size distributions and scattering phase functions have diminished impact on the accuracy of retrieved bulk microphysical parameters, permitting quite accurate retrievals of properties including the effective radius (up to 10%, or 0.03), and the radiatively important optical properties, such as the asymmetry factor (up to 4%, or ±0.02) and single-scattering albedo (up to 6%, or ±0.04). Also, the obtained results indicate that the uncertainties in the retrieved aerosol optical properties are quite small in the context of the calculated fluxes and direct aerosol radiative forcing (up to 15%, or 3 W∙m−2).</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2012-10-24</prism:publicationDate>
	<prism:volume>3</prism:volume>
	<prism:number>4</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos3040495</prism:doi>
	<prism:startingPage>495</prism:startingPage>
		<prism:endingPage>521</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Initial Assessment of the Spectrometer for Sky-Scanning, Sun-Tracking Atmospheric Research (4STAR)-Based Aerosol Retrieval: Sensitivity Study]]></dc:title>
    <dc:date>2012-10-24</dc:date>
	<dc:identifier>doi: 10.3390/atmos3040495</dc:identifier>
    	<dc:creator>Evgueni Kassianov</dc:creator>
		<dc:creator>Connor Flynn</dc:creator>
		<dc:creator>Jens Redemann</dc:creator>
		<dc:creator>Beat Schmid</dc:creator>
		<dc:creator>Philip Russell</dc:creator>
		<dc:creator>Alexander Sinyuk</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/3/4/468">
	<title><![CDATA[Atmosphere, Vol. 3, Pages 468-494: Development of a Ground Based Remote Sensing Approach for Direct Evaluation of Aerosol-Cloud Interaction]]></title>
	<link>http://www.mdpi.com/2073-4433/3/4/468</link>
	<description>The possible interaction and modification of cloud properties due to aerosols is one of the most poorly understood mechanisms within climate studies, resulting in the most significant uncertainty as regards radiation budgeting. In this study, we explore direct ground based remote sensing methods to assess the Aerosol-Cloud Indirect Effect directly, as space-borne retrievals are not directly suitable for simultaneous aerosol/cloud retrievals. To illustrate some of these difficulties, a statistical assessment of existing multispectral imagers on geostationary (e.g., GOES)/Moderate Resolution Imaging Spectroradiometer (MODIS) satellite retrievals of the Cloud Droplet Effective Radius (Reff) showed significant biases especially at larger solar zenith angles, further motivating the use of ground based remote sensing approaches. In particular, we discuss the potential of using a combined Microwave Radiometer (MWR)—Multi-Filter Rotating Shadowband Radiometer (MFRSR) system for real-time monitoring of Cloud Optical Depth (COD) and Cloud Droplet Effective Radius (Reff), which are combined with aerosol vertical properties from an aerosol lidar. An iterative approach combining the simultaneous observations from MFRSR and MWR are used to retrieve the COD and Reff for thick cloud cases and are extensively validated using the DoE Southern Great Plains (SGP) retrievals as well as regression based parameterized model retrievals. In addition, we account for uncertainties in background aerosol, surface albedo and the combined measurement uncertainties from the MWR and MFRSR in order to provide realistic uncertainty estimates, which is found to be ~10% for the parameter range of interest in Aerosol-Cloud Interactions. Finally, we analyze a particular case of possible aerosol-cloud interaction described in the literature at the SGP site and demonstrate that aerosol properties obtained at the surface can lead to inconclusive results in comparison to lidar-derived aerosol properties near the cloud base.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2012-10-17</prism:publicationDate>
	<prism:volume>3</prism:volume>
	<prism:number>4</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos3040468</prism:doi>
	<prism:startingPage>468</prism:startingPage>
		<prism:endingPage>494</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Development of a Ground Based Remote Sensing Approach for Direct Evaluation of Aerosol-Cloud Interaction]]></dc:title>
    <dc:date>2012-10-17</dc:date>
	<dc:identifier>doi: 10.3390/atmos3040468</dc:identifier>
    	<dc:creator>Bomidi Lakshmi Madhavan</dc:creator>
		<dc:creator>Yuzhe He</dc:creator>
		<dc:creator>Yonghua Wu</dc:creator>
		<dc:creator>Barry Gross</dc:creator>
		<dc:creator>Fred Moshary</dc:creator>
		<dc:creator>Samir Ahmed</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/3/4/451">
	<title><![CDATA[Atmosphere, Vol. 3, Pages 451-467: A Polarized Atmospheric Radiative Transfer Model for Calculations of Spectra of the Stokes Parameters of Shortwave Radiation Based on the Line-by-Line and Monte Carlo Methods]]></title>
	<link>http://www.mdpi.com/2073-4433/3/4/451</link>
	<description>This paper presents a new version of radiative transfer model called the Fast Line-by-Line Model (FLBLM), which is based on the Line-by-Line (LbL) and Monte Carlo (MC) methods and rigorously treats particulate and molecular scattering alongside absorption. The advantage of this model consists in the use of the line-by-line model that allows for the computing of high-resolution spectra quite quickly. We have developed the model by taking into account the polarization state of light and carried out some validations by comparison against benchmark results. FLBLM calculates the Stokes parameters spectra of shortwave radiation in vertically inhomogeneous atmospheres. This update makes the model applicable for the assessment of cloud and aerosol influence on radiances as measured by the SW high-resolution polarization spectrometers. In sample results we demonstrate that the high-resolution spectra of the Stokes parameters contain more detailed information about clouds and aerosols than the medium- and low-resolution spectra wherein lines are not resolved. The presented model is rapid enough for many practical applications (e.g., validations) and might be useful especially for the remote sensing. FLBLM is suitable for development of the reliable technique for retrieval of optical and microphysical properties of clouds and aerosols from high-resolution satellites data.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2012-10-10</prism:publicationDate>
	<prism:volume>3</prism:volume>
	<prism:number>4</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos3040451</prism:doi>
	<prism:startingPage>451</prism:startingPage>
		<prism:endingPage>467</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[A Polarized Atmospheric Radiative Transfer Model for Calculations of Spectra of the Stokes Parameters of Shortwave Radiation Based on the Line-by-Line and Monte Carlo Methods]]></dc:title>
    <dc:date>2012-10-10</dc:date>
	<dc:identifier>doi: 10.3390/atmos3040451</dc:identifier>
    	<dc:creator>Boris Fomin</dc:creator>
		<dc:creator>Victoria Falaleeva</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/3/3/419">
	<title><![CDATA[Atmosphere, Vol. 3, Pages 419-450: Evaluation of Two Cloud Parameterizations and Their Possible Adaptation to Arctic Climate Conditions]]></title>
	<link>http://www.mdpi.com/2073-4433/3/3/419</link>
	<description>Based on the atmospheric regional climate model HIRHAM5, the single-column model version HIRHAM5-SCM was developed and applied to investigate the performance of a relative humidity based (RH-Scheme) and a prognostic statistical cloud scheme (PS-Scheme) in the central Arctic. The surface pressure as well as dynamical tendencies of temperature, specific humidity, and horizontal wind were prescribed from the ERA-Interim data set to enable the simulation of a realistic annual cycle. Both modeled temperature and relative humidity profiles were validated against radio soundings carried out on the 35th North Pole drifting station (NP-35). Simulated total cloud cover was evaluated with NP-35 and satellite-based ISCCP-D2 and MODIS observations. The more sophisticated PS-Scheme was found to perform more realistically and matched the observations better. Nevertheless, the model systematically overestimated the monthly averaged total cloud cover. Sensitivity studies were conducted to assess the effect of modified “tuning” parameters on cloud-related model variables. Two tunable parameters of the PS-Scheme and six tuning parameters contained in the cloud microphysics were analyzed. Lower values of the PS-Scheme adjustment parameter q0, which defines the shape of the symmetric beta distribution (acting as probability density function), as well as higher values of the cloud water threshold CWmin or autoconversion rate γ1 are able to reduce the overestimation of Arctic clouds. Furthermore, a lower cloud ice threshold γthr, which controls the Bergeron–Findeisen process, improves model cloudiness and the ratio of liquid to solid water content.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2012-08-17</prism:publicationDate>
	<prism:volume>3</prism:volume>
	<prism:number>3</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos3030419</prism:doi>
	<prism:startingPage>419</prism:startingPage>
		<prism:endingPage>450</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Evaluation of Two Cloud Parameterizations and Their Possible Adaptation to Arctic Climate Conditions]]></dc:title>
    <dc:date>2012-08-17</dc:date>
	<dc:identifier>doi: 10.3390/atmos3030419</dc:identifier>
    	<dc:creator>Daniel Klaus</dc:creator>
		<dc:creator>Wolfgang Dorn</dc:creator>
		<dc:creator>Klaus Dethloff</dc:creator>
		<dc:creator>Annette Rinke</dc:creator>
		<dc:creator>Moritz Mielke</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/3/3/400">
	<title><![CDATA[Atmosphere, Vol. 3, Pages 400-418: Evaluation of the Variability in Chemical Transport Model Performance for Deposition and Ambient Concentrations of Nitrogen and Sulfur Compounds]]></title>
	<link>http://www.mdpi.com/2073-4433/3/3/400</link>
	<description>Air quality models are increasingly used to develop estimates of dry and wet deposition of sulfate and nitrate in watersheds (because of lack of measurements) in an effort to determine the acidifying deposition load into the aquatic systems. These models need to be rigorously evaluated to ensure that one can rely on the modeled quantities instead of the measured quantities. In the United State (U.S.), these models have been proposed for use in establishing national standards based on modeled quantities. The U.S. Environmental Protection Agency (EPA) is considering aquatic acidification as the main ecological endpoint of concern in determining the secondary national ambient air quality standards for nitrogen oxides and sulfur oxides. Acidification is tied to depositions of sulfur and nitrogen, which are linked to ambient concentrations of the elements. As EPA proposes to use a chemical transport model in linking deposition to ambient concentration, it is important to investigate how the currently used chemical transport models perform in predicting depositions and ambient concentrations of relevant chemical species and quantify the variability in their estimates. In this study, several annual simulations by multiple chemical transport models for the entire continental U.S. domain are evaluated against available measurement data for depositions and ambient concentrations of sulfur oxides and reactive nitrogen species. The model performance results vary by evaluation time-scale and geographical region. Evaluation of annualized quantities (annual average ambient concentrations and annual total depositions) suppresses the large variances shown in the evaluation using the observation’s native shorter-term time-scales (e.g., weekly). In addition, there is a large degree of bias and error (especially for deposition fluxes) in the modeling results that brings to question the suitability of using air quality models to provide estimates of deposition loads. Variability in the ratio of deposition to ambient concentration, so-called the Transference Ratio that EPA has proposed to use in linking deposition to ambient concentration, is also examined. Our study shows that the Transference Ratios as well as total reduced nitrogen deposition, another modeled parameter EPA proposed to use in the process of determining the new secondary standard, vary considerably by geographical region and by model simulation.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2012-08-10</prism:publicationDate>
	<prism:volume>3</prism:volume>
	<prism:number>3</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos3030400</prism:doi>
	<prism:startingPage>400</prism:startingPage>
		<prism:endingPage>418</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Evaluation of the Variability in Chemical Transport Model Performance for Deposition and Ambient Concentrations of Nitrogen and Sulfur Compounds]]></dc:title>
    <dc:date>2012-08-10</dc:date>
	<dc:identifier>doi: 10.3390/atmos3030400</dc:identifier>
    	<dc:creator>Bonyoung Koo</dc:creator>
		<dc:creator>Piti Piyachaturawat</dc:creator>
		<dc:creator>Ralph Morris</dc:creator>
		<dc:creator>Eladio Knipping</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/3/3/377">
	<title><![CDATA[Atmosphere, Vol. 3, Pages 377-399: Spatio-Temporal Variability of Western Central African Convection from Infrared Observations]]></title>
	<link>http://www.mdpi.com/2073-4433/3/3/377</link>
	<description>The present study has used Meteosat infrared brightness temperature images to investigate the regional and interannual variability of Central African cloudiness. Spatial and temporal variability were investigated using half–hourly data from the Meteosat-7 during June–July–August (JJA) of 1998–2002. The full domain of study (1.5E–17E, 1N–15N) was divided into six regions and statistics in each region were derived. Analysis of the dependence of cloud fraction to the brightness temperature threshold is explored both over land and ocean. Three diurnal cycle regimes (continental, oceanic, and coastal) are depicted according to the amplitude and peak time. Over regions of relatively flat terrain, results indicate enhancement of deep convection in the afternoon followed by a gradual decrease in the night. The diurnal cycle of convection is characterised by afternoon and early evening (around 15:00–18:00 LST) maxima located mainly downwind of the major mountain chains, and a more rapid nighttime decay. In terms of the harmonic amplitude, the diurnal signal shows significant regional contrast with the strongest manifestation over the Adamaoua Plateau and the weakest near the South Cameroon Plateau. This remarkable spatial dependence is clear evidence of orographic and heterogeneous land-surface impacts on convective development. Oceanic region exhibits weak activity of convective cloudiness with a maximum at noon. It is suggested that daytime heating of the land surface and moist environment may play a role in determining the spatial distribution of cloud fraction. This study further demonstrates the importance of the Cameroon coastline concavity and coastal mountains in regulating regional frequencies of convection and their initialization. The strength of the diurnal cycle of convective activity depends on mountain height, mean flow, coastal geometry.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2012-08-08</prism:publicationDate>
	<prism:volume>3</prism:volume>
	<prism:number>3</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos3030377</prism:doi>
	<prism:startingPage>377</prism:startingPage>
		<prism:endingPage>399</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Spatio-Temporal Variability of Western Central African Convection from Infrared Observations]]></dc:title>
    <dc:date>2012-08-08</dc:date>
	<dc:identifier>doi: 10.3390/atmos3030377</dc:identifier>
    	<dc:creator>Derbetini A. Vondou</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/3/3/352">
	<title><![CDATA[Atmosphere, Vol. 3, Pages 352-376: Modeling Multiple-Core Updraft Plume Rise for an Aerial Ignition Prescribed Burn by Coupling Daysmoke with a Cellular Automata Fire Model]]></title>
	<link>http://www.mdpi.com/2073-4433/3/3/352</link>
	<description>Smoke plume rise is critically dependent on plume updraft structure. Smoke plumes from landscape burns (forest and agricultural burns) are typically structured into “sub-plumes” or multiple-core updrafts with the number of updraft cores depending on characteristics of the landscape, fire, fuels, and weather. The number of updraft cores determines the efficiency of vertical transport of heat and particulate matter and therefore plume rise. Daysmoke, an empirical-stochastic plume rise model designed for simulating wildland fire plumes, requires updraft core number as an input. In this study, updraft core number was gained via a cellular automata fire model applied to an aerial ignition prescribed burn conducted at Eglin AFB on 6 February 2011. Typically four updraft cores were simulated in agreement with a photo-image of the plume showing three/four distinct sub-plumes. Other Daysmoke input variables were calculated including maximum initial updraft core diameter, updraft core vertical velocity, and relative emissions production. Daysmoke simulated a vertical tower that mushroomed 1,000 m above the mixing height. Plume rise was validated by ceilometer. Simulations with two temperature profiles found 89–93 percent of the PM2.5 released during the flaming phase was transported into the free atmosphere above the mixing layer. The minimal ground-level smoke concentrations were verified by a small network of particulate samplers. Implications of these results for inclusion of wildland fire smoke in air quality models are discussed.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2012-07-25</prism:publicationDate>
	<prism:volume>3</prism:volume>
	<prism:number>3</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos3030352</prism:doi>
	<prism:startingPage>352</prism:startingPage>
		<prism:endingPage>376</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Modeling Multiple-Core Updraft Plume Rise for an Aerial Ignition Prescribed Burn by Coupling Daysmoke with a Cellular Automata Fire Model]]></dc:title>
    <dc:date>2012-07-25</dc:date>
	<dc:identifier>doi: 10.3390/atmos3030352</dc:identifier>
    	<dc:creator>Gary L. Achtemeier</dc:creator>
		<dc:creator>Scott A. Goodrick</dc:creator>
		<dc:creator>Yongqiang Liu</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/3/3/320">
	<title><![CDATA[Atmosphere, Vol. 3, Pages 320-351: The Spring-Time Boundary Layer in the Central Arctic Observed during PAMARCMiP 2009]]></title>
	<link>http://www.mdpi.com/2073-4433/3/3/320</link>
	<description>The Arctic atmospheric boundary layer (AABL) in the central Arctic was characterized by dropsonde, lidar, ice thickness and airborne in situ measurements during the international Polar Airborne Measurements and Arctic Regional Climate Model Simulation Project (PAMARCMiP) in April 2009. We discuss AABL observations in the lowermost 500 m above (A) open water, (B) sea ice with many open/refrozen leads (C) sea ice with few leads, and (D) closed sea ice with a front modifying the AABL. Above water, the AABL had near-neutral stratification and contained a high water vapor concentration. Above sea ice, a low AABL top, low near-surface temperatures, strong surface-based temperature inversions and an increase of moisture with altitude were observed. AABL properties and particle concentrations were modified by a frontal system, allowing vertical mixing with the free atmosphere. Above areas with many leads, the potential temperature decreased with height in the lowest 50 m and was nearly constant above, up to an altitude of 100–200 m, indicating vertical mixing. The increase of the backscatter coefficient towards the surface was high. Above sea ice with few refrozen leads, the stably stratified boundary layer extended up to 200–300 m altitude. It was characterized by low specific humidity and a smaller increase of the backscatter coefficient towards the surface.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2012-07-16</prism:publicationDate>
	<prism:volume>3</prism:volume>
	<prism:number>3</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos3030320</prism:doi>
	<prism:startingPage>320</prism:startingPage>
		<prism:endingPage>351</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[The Spring-Time Boundary Layer in the Central Arctic Observed during PAMARCMiP 2009]]></dc:title>
    <dc:date>2012-07-16</dc:date>
	<dc:identifier>doi: 10.3390/atmos3030320</dc:identifier>
    	<dc:creator>Astrid Lampert</dc:creator>
		<dc:creator>Marion Maturilli</dc:creator>
		<dc:creator>Christoph Ritter</dc:creator>
		<dc:creator>Anne Hoffmann</dc:creator>
		<dc:creator>Maria Stock</dc:creator>
		<dc:creator>Andreas Herber</dc:creator>
		<dc:creator>Gerit Birnbaum</dc:creator>
		<dc:creator>Roland Neuber</dc:creator>
		<dc:creator>Klaus Dethloff</dc:creator>
		<dc:creator>Thomas Orgis</dc:creator>
		<dc:creator>Robert Stone</dc:creator>
		<dc:creator>Ralf Brauner</dc:creator>
		<dc:creator>Johannes Kässbohrer</dc:creator>
		<dc:creator>Christian Haas</dc:creator>
		<dc:creator>Alexander Makshtas</dc:creator>
		<dc:creator>Vladimir Sokolov</dc:creator>
		<dc:creator>Peter Liu</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/3/3/288">
	<title><![CDATA[Atmosphere, Vol. 3, Pages 288-319: Assessment of the Weather Research and Forecasting/Chemistry Model to Simulate Ozone Concentrations in March 2008 over Coastal Areas of the Sea of Japan]]></title>
	<link>http://www.mdpi.com/2073-4433/3/3/288</link>
	<description>The fully coupled WRF/Chem (Weather Research and Forecasting/Chemistry) model is used to simulate air quality over coastal areas of the Sea of Japan. The anthropogenic surface emissions database used as input for this model was based primarily on global hourly emissions data (dust, sea salt, and biomass burning), RETRO (REanalysis of the TROpospheric chemical composition), GEIA (Global Emissions Inventory Activity), and POET (Precursors of Ozone and their Effects in the Troposphere). Climatologic concentrations of particulate matter derived from the Regional Acid Deposition Model (RADM2), chemical mechanism, and the Secondary Organic Aerosol Model (MADE/SORGAM) with aqueous reactions were used to deduce the corresponding aerosol fluxes for input to the WRF/Chem model. The model was first integrated continuously over 48 hours, starting from 00:00 UTC on 14 March 2008, to evaluate ozone concentrations and other precursor pollutants. WPS meteorological data were used for the WRF/Chem model simulation in this study. Despite the low resolution of global emissions and the weak density of the local point emissions, it was found that the WRF/Chem model simulates the diurnal variation of the chemical species concentrations over the coastal areas of the Sea of Japan quite well. The Air Quality Management Division of the Ministry of the Environment in Japan selected the maximum level of the air quality standard for ozone, which is 60 ppb. In this study, the atmospheric concentrations of ozone over the coastal area of the Sea of Japan were calculated to be 30–55 ppb during the simulation period, which was lower than the Japanese air quality standard for ozone.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2012-07-10</prism:publicationDate>
	<prism:volume>3</prism:volume>
	<prism:number>3</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos3030288</prism:doi>
	<prism:startingPage>288</prism:startingPage>
		<prism:endingPage>319</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Assessment of the Weather Research and Forecasting/Chemistry Model to Simulate Ozone Concentrations in March 2008 over Coastal Areas of the Sea of Japan]]></dc:title>
    <dc:date>2012-07-10</dc:date>
	<dc:identifier>doi: 10.3390/atmos3030288</dc:identifier>
    	<dc:creator>Khandakar Md. Habib Al Razi</dc:creator>
		<dc:creator>Moritomi Hiroshi</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/3/2/266">
	<title><![CDATA[Atmosphere, Vol. 3, Pages 266-287: An Examination of the Sensitivity of Sulfur Dioxide, Nitric Oxide, and Nitrogen Dioxide Concentrations to the Important Factors Affecting Air Quality Inside a Public Transportation Bus]]></title>
	<link>http://www.mdpi.com/2073-4433/3/2/266</link>
	<description>The present study examined the sensitivity of sulfur dioxide (SO2), nitric oxide (NO), and nitrogen dioxide (NO2) concentrations to the important factors affecting air quality inside a public transportation bus. Additionally, this study quantified the in-bus contaminant concentrations in relation to the ranked statistically significant variables. The independent variables to which the monitored contaminant concentrations are the most sensitive to were determined using regression trees and the analysis of variance. A comprehensive one-year database, of the monitored contaminant concentrations and the independent factors that affect an indoor microenvironment (meteorology, monitoring periods, outdoor sources, and ventilation settings) was developed to study the sensitivity of monitored in-bus contaminants. SO2 concentrations were extremely sensitive to the month, weather conditions, and heavy vehicles. NO concentrations were sensitive to the month/season, ventilation, and ambient temperature; while NO2 concentrations were additionally sensitive to the monitoring period and the ambient mixing ratio. Quantified in-bus relationships revealed NO and NO2 concentrations to be less than 0.6 ppm and 0.1 ppm, respectively. SO2 concentrations of 0.4 ppm were observed in the fall-winter months, when the lead heavy vehicles were at a minimum density of 56 per hour; &amp;lt; 0.4 ppm SO2 concentrations remained for the rest of the year.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2012-06-15</prism:publicationDate>
	<prism:volume>3</prism:volume>
	<prism:number>2</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos3020266</prism:doi>
	<prism:startingPage>266</prism:startingPage>
		<prism:endingPage>287</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[An Examination of the Sensitivity of Sulfur Dioxide, Nitric Oxide, and Nitrogen Dioxide Concentrations to the Important Factors Affecting Air Quality Inside a Public Transportation Bus]]></dc:title>
    <dc:date>2012-06-15</dc:date>
	<dc:identifier>doi: 10.3390/atmos3020266</dc:identifier>
    	<dc:creator>Akhil Kadiyala</dc:creator>
		<dc:creator>Ashok Kumar</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/3/2/246">
	<title><![CDATA[Atmosphere, Vol. 3, Pages 246-265: Estimation of the Interference in Multi-Gas Measurements Using Infrared Photoacoustic Analyzers]]></title>
	<link>http://www.mdpi.com/2073-4433/3/2/246</link>
	<description>Two methods were described to estimate interference in the measurements of infrared (IR) photoacoustic multi-gas analyzer (PAMGA). One is IR spectroscopic analysis (IRSA) and the other is mathematical simulation. An Innova 1412 analyzer (AirTech Instruments, Ballerup, Denmark) with two different filter configurations was used to provide examples that demonstrate the two methods. The filter configuration in Example #1 consists of methane (CH4), methanol (MeOH), ethanol (EtOH), nitrous oxide (N2O), carbon dioxide (CO2), and water vapor (H2O), and in Example #2 of ammonia (NH3), MeOH, EtOH, N2O, CO2, and H2O. The interferences of NH3 as a non-target gas in Example #1 were measured to validate the two methods. The interferences of H2O and NH3 as target gases in Example #2 were also measured to evaluate the analyzer’s internal cross compensation algorithm. Both simulation and experimental results showed that the interference between the target gases could be eliminated by the internal cross compensation algorithm. But the interferences of non-target gases on target gases could not be addressed by the internal cross compensation, while they could be assessed by the IRSA and mathematical simulation methods. If the IR spectrum of a non-target gas overlaps with that of target gas A at filter A, it could affect not only gas A (primary interference), but also other target gases by secondary interference (because the IR spectrum of gas A overlaps with gas B at filter B and thus affects gas B measurements). The IRSA and mathematical simulation methods can be used to estimate the interference in IR PAMGA measurements prior to purchase or calibration of the unit.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2012-04-18</prism:publicationDate>
	<prism:volume>3</prism:volume>
	<prism:number>2</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos3020246</prism:doi>
	<prism:startingPage>246</prism:startingPage>
		<prism:endingPage>265</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Estimation of the Interference in Multi-Gas Measurements Using Infrared Photoacoustic Analyzers]]></dc:title>
    <dc:date>2012-04-18</dc:date>
	<dc:identifier>doi: 10.3390/atmos3020246</dc:identifier>
    	<dc:creator>Yongjing Zhao</dc:creator>
		<dc:creator>Yuee Pan</dc:creator>
		<dc:creator>Jerry Rutherford</dc:creator>
		<dc:creator>Frank M. Mitloehner</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/3/1/229">
	<title><![CDATA[Atmosphere, Vol. 3, Pages 229-245: Unveiling Assigned Amount Unit (AAU) Trades: Current Market Impacts and Prospects for the Future]]></title>
	<link>http://www.mdpi.com/2073-4433/3/1/229</link>
	<description>The sale of assigned amount units (AAUs) from countries whose emissions have declined since their baseline year under the Kyoto Protocol has led critics to be skeptical of carbon markets due to the lack of actual emission reductions that occur as a result of these trades. This policy review describes the historical context of AAU trading, current market price and volumes, and environmental and economic impacts of the current AAU trading rules. Options for how to handle current, and prevent the creation of future, surplus AAUs are discussed.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2012-03-07</prism:publicationDate>
	<prism:volume>3</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos3010229</prism:doi>
	<prism:startingPage>229</prism:startingPage>
		<prism:endingPage>245</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Unveiling Assigned Amount Unit (AAU) Trades: Current Market Impacts and Prospects for the Future]]></dc:title>
    <dc:date>2012-03-07</dc:date>
	<dc:identifier>doi: 10.3390/atmos3010229</dc:identifier>
    	<dc:creator>Elizabeth Lokey Aldrich</dc:creator>
		<dc:creator>Cassandra L. Koerner</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/3/1/213">
	<title><![CDATA[Atmosphere, Vol. 3, Pages 213-228: Numerical Simulation of the Global Neutral Wind System of the Earth’s Middle Atmosphere for Different Seasons]]></title>
	<link>http://www.mdpi.com/2073-4433/3/1/213</link>
	<description>A non-hydrostatic model of the global neutral wind system of the Earth’s atmosphere, developed earlier, is utilized to simulate the large-scale global circulation of the middle atmosphere for conditions of different seasons. In the model calculations, not only the horizontal components, but also the vertical component of the neutral wind velocity, are obtained by means of a numerical solution of a generalized Navier-Stokes equation for compressible gas, so the hydrostatic equation is not applied. Moreover, the global temperature field is assumed to be a given distribution, (i.e., the input parameter of the model) and obtained from one of the existing empirical models. The results of simulation indicate that the horizontal non-uniformity of the neutral gas temperature, which is distinct in different seasons, ought to considerably influence the formation of the global neutral wind system in the middle atmosphere, in particular, the large-scale circumpolar vortices of the northern and southern hemispheres.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2012-03-05</prism:publicationDate>
	<prism:volume>3</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos3010213</prism:doi>
	<prism:startingPage>213</prism:startingPage>
		<prism:endingPage>228</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Numerical Simulation of the Global Neutral Wind System of the Earth’s Middle Atmosphere for Different Seasons]]></dc:title>
    <dc:date>2012-03-05</dc:date>
	<dc:identifier>doi: 10.3390/atmos3010213</dc:identifier>
    	<dc:creator>Igor V. Mingalev</dc:creator>
		<dc:creator>Victor S. Mingalev</dc:creator>
		<dc:creator>Galina I. Mingaleva</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/3/1/200">
	<title><![CDATA[Atmosphere, Vol. 3, Pages 200-212: Anthropogenic Climate Change and Allergic Diseases]]></title>
	<link>http://www.mdpi.com/2073-4433/3/1/200</link>
	<description>Climate change is expected to have an impact on various aspects of health, including mucosal areas involved in allergic inflammatory disorders that include asthma, allergic rhinitis, allergic conjunctivitis and anaphylaxis. The evidence that links climate change to the exacerbation and the development of allergic disease is increasing and appears to be linked to changes in pollen seasons (duration, onset and intensity) and changes in allergen content of plants and their pollen as it relates to increased sensitization, allergenicity and exacerbations of allergic airway disease. This has significant implications for air quality and for the global food supply.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2012-02-28</prism:publicationDate>
	<prism:volume>3</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Review</prism:section>
	<prism:doi>10.3390/atmos3010200</prism:doi>
	<prism:startingPage>200</prism:startingPage>
		<prism:endingPage>212</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Anthropogenic Climate Change and Allergic Diseases]]></dc:title>
    <dc:date>2012-02-28</dc:date>
	<dc:identifier>doi: 10.3390/atmos3010200</dc:identifier>
    	<dc:creator>James Blando</dc:creator>
		<dc:creator>Leonard Bielory</dc:creator>
		<dc:creator>Viann Nguyen</dc:creator>
		<dc:creator>Rafael Diaz</dc:creator>
		<dc:creator>Hueiwang Anna Jeng</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/3/1/181">
	<title><![CDATA[Atmosphere, Vol. 3, Pages 181-199: Assessing the Transferability of the Regional Climate Model REMO to Different COordinated Regional Climate Downscaling EXperiment (CORDEX) Regions]]></title>
	<link>http://www.mdpi.com/2073-4433/3/1/181</link>
	<description>The transferability of the regional climate model REMO with a standard setup over different regions of the world has been evaluated. The study is based on the idea that the modeling parameters and parameterizations in a regional climate model should be robust to adequately simulate the major climatic characteristic of different regions around the globe. If a model is not able to do that, there might be a chance of an “overtuning” to the “home-region”, which means that the model physics are tuned in a way that it might cover some more fundamental errors, e.g., in the dynamics. All simulations carried out in this study contribute to the joint effort by the international regional downscaling community called COordinated Regional climate Downscaling EXperiment (CORDEX). REMO has been integrated over six CORDEX domains forced with the so-called perfect boundary conditions obtained from the global reanalysis dataset ERA-Interim for the period 1989 to 2008. These six domains include Africa, Europe, North America, South America, West Asia and the Mediterranean region. Each of the six simulations was conducted with the identical model setup which allows investigating the transferability of a single model to regions with substantially different climate characteristics. For the consistent evaluation over the different domains, a new evaluation framework is presented by combining the Köppen-Trewartha climate classification with temperature-precipitation relationship plots and a probability density function (PDF) skill score method. The evaluation of the spatial and temporal characteristics of simulated precipitation and temperature, in comparison to observational datasets, shows that REMO is able to simulate the mean annual climatic features over all the domains quite reasonably, but still some biases remain. The regions over the Amazon and near the coast of major upwelling regions have a significant warm bias. Wet and dry biases appear over the mountainous regions and East Africa, respectively. The temperature over South America and precipitation over the tundra and highland climate of West Asia are misrepresented. The probable causes leading to these biases are discussed and ideas for improvements are suggested. The annual cycle of precipitation and temperature of major catchments in each domain are also well represented by REMO. The model has performed well in simulating the inter- and intra-seasonal characteristics of different climate types in different regions. Moreover, the model has a high ability in representing the general characteristics of different climate types as measured by the probability density function (PDF) skill score method. Although REMO seems to perform best over its home domain in Europe (domain of development and testing), the model has simulated quite well the climate characteristics of other regions with the same set of parameterization options. Therefore, these results lead us to the conclusion that REMO is well suited for long-term climate change simulations to examine projected future changes in all these regions.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2012-02-21</prism:publicationDate>
	<prism:volume>3</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos3010181</prism:doi>
	<prism:startingPage>181</prism:startingPage>
		<prism:endingPage>199</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Assessing the Transferability of the Regional Climate Model REMO to Different COordinated Regional Climate Downscaling EXperiment (CORDEX) Regions]]></dc:title>
    <dc:date>2012-02-21</dc:date>
	<dc:identifier>doi: 10.3390/atmos3010181</dc:identifier>
    	<dc:creator>Daniela Jacob</dc:creator>
		<dc:creator>Alberto Elizalde</dc:creator>
		<dc:creator>Andreas Haensler</dc:creator>
		<dc:creator>Stefan Hagemann</dc:creator>
		<dc:creator>Pankaj Kumar</dc:creator>
		<dc:creator>Ralf Podzun</dc:creator>
		<dc:creator>Diana Rechid</dc:creator>
		<dc:creator>Armelle Reca Remedio</dc:creator>
		<dc:creator>Fahad Saeed</dc:creator>
		<dc:creator>Kevin Sieck</dc:creator>
		<dc:creator>Claas Teichmann</dc:creator>
		<dc:creator>Christof Wilhelm</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/3/1/164">
	<title><![CDATA[Atmosphere, Vol. 3, Pages 164-180: Pre-Harvest Sugarcane Burning: Determination of Emission Factors through Laboratory Measurements]]></title>
	<link>http://www.mdpi.com/2073-4433/3/1/164</link>
	<description>Sugarcane is an important crop for the Brazilian economy and roughly 50% of its production is used to produce ethanol. However, the common practice of pre-harvest burning of sugarcane straw emits particulate material, greenhouse gases, and tropospheric ozone precursors to the atmosphere. Even with policies to eliminate the practice of pre-harvest sugarcane burning in the near future, there is still significant environmental damage. Thus, the generation of reliable inventories of emissions due to this activity is crucial in order to assess their environmental impact. Nevertheless, the official Brazilian emissions inventory does not presently include the contribution from pre-harvest sugarcane burning. In this context, this work aims to determine sugarcane straw burning emission factors for some trace gases and particulate material smaller than 2.5 μm in the laboratory. Excess mixing ratios for CO2, CO, NOX, UHC (unburned hydrocarbons), and PM2.5 were measured, allowing the estimation of their respective emission factors. Average estimated values for emission factors (g kg−1 of burned dry biomass) were 1,303 ± 218 for CO2, 65 ± 14 for CO, 1.5 ± 0.4 for NOX, 16 ± 6 for UHC, and 2.6 ± 1.6 for PM2.5. These emission factors can be used to generate more realistic emission inventories and therefore improve the results of air quality models.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2012-02-15</prism:publicationDate>
	<prism:volume>3</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos3010164</prism:doi>
	<prism:startingPage>164</prism:startingPage>
		<prism:endingPage>180</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Pre-Harvest Sugarcane Burning: Determination of Emission Factors through Laboratory Measurements]]></dc:title>
    <dc:date>2012-02-15</dc:date>
	<dc:identifier>doi: 10.3390/atmos3010164</dc:identifier>
    	<dc:creator>Daniela de Azeredo França</dc:creator>
		<dc:creator>Karla Maria Longo</dc:creator>
		<dc:creator>Turibio Gomes Soares Neto</dc:creator>
		<dc:creator>José Carlos Santos</dc:creator>
		<dc:creator>Saulo R. Freitas</dc:creator>
		<dc:creator>Bernardo F. T. Rudorff</dc:creator>
		<dc:creator>Ely Vieira Cortez</dc:creator>
		<dc:creator>Edson Anselmo</dc:creator>
		<dc:creator>João Andrade Carvalho</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/3/1/132">
	<title><![CDATA[Atmosphere, Vol. 3, Pages 132-163: The Impact of Uncertainties in African Biomass Burning Emission Estimates on Modeling Global Air Quality, Long Range Transport and Tropospheric Chemical Lifetimes]]></title>
	<link>http://www.mdpi.com/2073-4433/3/1/132</link>
	<description>The chemical composition of the troposphere in the tropics and Southern Hemisphere (SH) is significantly influenced by gaseous emissions released from African biomass burning (BB). Here we investigate how various emission estimates given in bottom-up BB inventories (GFEDv2, GFEDv3, AMMABB) affect simulations of global tropospheric composition using the TM4 chemistry transport model. The application of various model parameterizations for introducing such emissions is also investigated. There are perturbations in near-surface ozone (O3) and carbon monoxide (CO) of ~60–90% in the tropics and ~5–10% in the SH between different inventories. Increasing the update frequency of the temporal distribution to eight days generally results in decreases of between ~5 and 10% in near-surface mixing ratios throughout the tropics, which is larger than the influence of increasing the injection heights at which BB emissions are introduced. There are also associated differences in the long range transport of pollutants throughout the SH, where the composition of the free troposphere in the SH is sensitive to the chosen BB inventory. Analysis of the chemical budget terms reveals that the influence of increasing the tropospheric CO burden due to BB on oxidative capacity of the troposphere is mitigated by the associated increase in NOx emissions (and thus O3) with the variations in the CO/N ratio between inventories being low. For all inventories there is a decrease in the tropospheric chemical lifetime of methane of between 0.4 and 0.8% regardless of the CO emitted from African BB. This has implications for assessing the effect of inter-annual variability in BB on the annual growth rate of methane.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2012-02-09</prism:publicationDate>
	<prism:volume>3</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos3010132</prism:doi>
	<prism:startingPage>132</prism:startingPage>
		<prism:endingPage>163</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[The Impact of Uncertainties in African Biomass Burning Emission Estimates on Modeling Global Air Quality, Long Range Transport and Tropospheric Chemical Lifetimes]]></dc:title>
    <dc:date>2012-02-09</dc:date>
	<dc:identifier>doi: 10.3390/atmos3010132</dc:identifier>
    	<dc:creator>Jason E. Williams</dc:creator>
		<dc:creator>Michiel van Weele</dc:creator>
		<dc:creator>Peter F. J. van Velthoven</dc:creator>
		<dc:creator>Marinus P. Scheele</dc:creator>
		<dc:creator>Catherine Liousse</dc:creator>
		<dc:creator>Guido R. van der Werf</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/3/1/124">
	<title><![CDATA[Atmosphere, Vol. 3, Pages 124-131: Trends in Intense Typhoon Minimum Sea Level Pressure]]></title>
	<link>http://www.mdpi.com/2073-4433/3/1/124</link>
	<description>A number of recent publications have examined trends in the maximum wind speed of tropical cyclones in various basins. In this communication, the author focuses on typhoons in the western North Pacific. Rather than maximum wind speed, the intensity of the storms is measured by their lifetime minimum sea level pressure (MSLP). Quantile regression is used to test for trends in storms of extreme intensity. The results indicate that there is a trend of decreasing intensity in the most intense storms as measured by MSLP over the period 1951–2010. However, when the data are broken into intervals 1951–1987 and 1987–2010, neither interval has a significant trend, but the intensity quantiles for the two periods differ. Reasons for this are discussed, including the cessation of aircraft reconnaissance in 1987. The author also finds that the average typhoon intensity is greater in El Nino years, while the intensity of the strongest typhoons shows no significant relation to El Nino Southern Oscillation.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2012-01-31</prism:publicationDate>
	<prism:volume>3</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Communication</prism:section>
	<prism:doi>10.3390/atmos3010124</prism:doi>
	<prism:startingPage>124</prism:startingPage>
		<prism:endingPage>131</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Trends in Intense Typhoon Minimum Sea Level Pressure]]></dc:title>
    <dc:date>2012-01-31</dc:date>
	<dc:identifier>doi: 10.3390/atmos3010124</dc:identifier>
    	<dc:creator>Stephen L. Durden</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/3/1/103">
	<title><![CDATA[Atmosphere, Vol. 3, Pages 103-123: An Evaluation of Modeled Plume Injection Height with Satellite-Derived Observed Plume Height]]></title>
	<link>http://www.mdpi.com/2073-4433/3/1/103</link>
	<description>Plume injection height influences plume transport characteristics, such as range and potential for dilution. We evaluated plume injection height from a predictive wildland fire smoke transport model over the contiguous United States (U.S.) from 2006 to 2008 using satellite-derived information, including plume top heights from the Multi-angle Imaging SpectroRadiometer (MISR) Plume Height Climatology Project and aerosol vertical profiles from the Cloud-Aerosol Lidar with Orthogonal Polarization (CALIOP). While significant geographic variability was found in the comparison between modeled plumes and satellite-detected plumes, modeled plume heights were lower overall. In the eastern U.S., satellite-detected and modeled plume heights were similar (median height 671 and 660 m respectively). Both satellite-derived and modeled plume injection heights were higher in the western U.S. (2345 and 1172 m, respectively). Comparisons of modeled plume injection height to satellite-derived plume height at the fire location (R2 = 0.1) were generally worse than comparisons done downwind of the fire (R2 = 0.22). This suggests that the exact injection height is not as important as placement of the plume in the correct transport layer for transport modeling.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2012-01-18</prism:publicationDate>
	<prism:volume>3</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos3010103</prism:doi>
	<prism:startingPage>103</prism:startingPage>
		<prism:endingPage>123</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[An Evaluation of Modeled Plume Injection Height with Satellite-Derived Observed Plume Height]]></dc:title>
    <dc:date>2012-01-18</dc:date>
	<dc:identifier>doi: 10.3390/atmos3010103</dc:identifier>
    	<dc:creator>Sean M. Raffuse</dc:creator>
		<dc:creator>Kenneth J. Craig</dc:creator>
		<dc:creator>Narasimhan K. Larkin</dc:creator>
		<dc:creator>Tara T. Strand</dc:creator>
		<dc:creator>Dana Coe Sullivan</dc:creator>
		<dc:creator>Neil J. M. Wheeler</dc:creator>
		<dc:creator>Robert Solomon</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/3/1/87">
	<title><![CDATA[Atmosphere, Vol. 3, Pages 87-102: Atmosphere: A Source of Pathogenic or Beneficial Microbes?]]></title>
	<link>http://www.mdpi.com/2073-4433/3/1/87</link>
	<description>The atmosphere has been described as one of the last frontiers of biological exploration on Earth. The composition of microbial communities in the atmosphere is still not well-defined, and taxonomic studies of bacterial diversity in the outdoor air have just started to emerge, whereas our knowledge about the functional potential of air microbiota is scant. When in the air, microorganisms can be attached to ambient particles and/or incorporated into water droplets of clouds, fog, and precipitation (i.e., rain, snow, hail). Further, they can be deposited back to earth’s surfaces via dry and wet deposition processes and they can possibly induce an effect on the diversity and function of aquatic and terrestrial ecosystems or impose impacts to human health through microbial pathogens dispersion. In addition to their impact on ecosystem and public health, there are strong indications that air microbes are metabolically active and well adapted to the harsh atmospheric conditions. Furthermore they can affect atmospheric chemistry and physics, with important implications in meteorology and global climate. This review summarizes current knowledge about the ubiquitous presence of microbes in the atmosphere and discusses their ability to survive in the atmospheric environment. The purpose is to evaluate the atmospheric environment as a source of pathogenic or beneficial microbes and to assess the biotechnological opportunities that may offer.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2012-01-16</prism:publicationDate>
	<prism:volume>3</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Review</prism:section>
	<prism:doi>10.3390/atmos3010087</prism:doi>
	<prism:startingPage>87</prism:startingPage>
		<prism:endingPage>102</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Atmosphere: A Source of Pathogenic or Beneficial Microbes?]]></dc:title>
    <dc:date>2012-01-16</dc:date>
	<dc:identifier>doi: 10.3390/atmos3010087</dc:identifier>
    	<dc:creator>Paraskevi N. Polymenakou</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/3/1/59">
	<title><![CDATA[Atmosphere, Vol. 3, Pages 59-86: An Investigation of Two Highest Ozone Episodes During the Last Decade in New England]]></title>
	<link>http://www.mdpi.com/2073-4433/3/1/59</link>
	<description>This study examined the role of meteorological processes in two of the highest ozone (O3) episodes within the last decade at monitoring sites in southern New Hampshire (NH), USA. The highest O3 levels occurred on 14 August 2002 at Thompson Farm (TF) and 22 July 2004 at Castle Springs (CS). Ozone mixing ratios in the 2002 episode showed continual high values (&amp;gt;100 ppbv) at the beginning of the episode, and reached 151 ppbv on 14 August. The 2004 episode consisted of one day of high O3 (&amp;gt;100 ppbv) on 22 July at CS with the peak level of 111 ppbv. Our analysis suggested that the August 2002 high O3 event at TF occurred under stagnant synoptic high-pressure conditions that prevailed over the entire eastern USA for an unusually extended time period. The clear skies and stable meteorological conditions resulted in accumulation of pollutants in the boundary layer. At the same time, the mesoscale low-level-jet (LLJ) played an important role in transporting air masses from the polluted Mid-Atlantic areas to the Northeast. Local land-sea-breeze circulations also added to the impact of this event. Our examination showed that the unprecedented high levels of O3 on 22 July 2004 at CS was driven by two mechanisms, stratospheric intrusion and the Appalachian lee trough (APLT), which was not found during other O3 episodes at the site in the decade long data record. This study demonstrated that unusually high O3 levels at New England rural sites were driven by multi-scale processes, and the regional/local scale processes controlled the magnitude and timing of the local pollution episodes.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2011-12-27</prism:publicationDate>
	<prism:volume>3</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos3010059</prism:doi>
	<prism:startingPage>59</prism:startingPage>
		<prism:endingPage>86</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[An Investigation of Two Highest Ozone Episodes During the Last Decade in New England]]></dc:title>
    <dc:date>2011-12-27</dc:date>
	<dc:identifier>doi: 10.3390/atmos3010059</dc:identifier>
    	<dc:creator>Tzu-Ling Lai</dc:creator>
		<dc:creator>Robert Talbot</dc:creator>
		<dc:creator>Huiting Mao</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/3/1/33">
	<title><![CDATA[Atmosphere, Vol. 3, Pages 33-58: Radar-Based Analysis of Convective Storms over Northwestern Italy]]></title>
	<link>http://www.mdpi.com/2073-4433/3/1/33</link>
	<description>Thunderstorms may cause large damages to infrastructures and population, therefore the possible identification of the areas with the highest occurrence of these events is especially relevant. Nevertheless, few extensive studies of these phenomena with high spatial and temporal resolution have been carried out in the Alps and none of them includes North-western Italy. To analyze thunderstorm events, the data of the meteorological radar network of the regional meteorological service of Piedmont region (ARPA Piemonte) have been used in this work. The database analyzed includes all thunderstorms occurred during the warm months (April to September) of a 6-year period (2005–2010). The tracks of each storm have been evaluated using a storm tracking algorithm. Several characteristics of the storms have been analyzed, such as the duration, the spatial and the temporaldistribution, the direction and the distance travelled. Obtained results revealed several important characteristics that may be useful for nowcasting purposes providing a first attempt of radar-based climatology in the considered region.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2011-12-27</prism:publicationDate>
	<prism:volume>3</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos3010033</prism:doi>
	<prism:startingPage>33</prism:startingPage>
		<prism:endingPage>58</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Radar-Based Analysis of Convective Storms over Northwestern Italy]]></dc:title>
    <dc:date>2011-12-27</dc:date>
	<dc:identifier>doi: 10.3390/atmos3010033</dc:identifier>
    	<dc:creator>Paolo Davini</dc:creator>
		<dc:creator>Renzo Bechini</dc:creator>
		<dc:creator>Roberto Cremonini</dc:creator>
		<dc:creator>Claudio Cassardo</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/3/1/1">
	<title><![CDATA[Atmosphere, Vol. 3, Pages 1-32: A Review of Tropospheric Atmospheric Chemistry and Gas-Phase Chemical Mechanisms for Air Quality Modeling]]></title>
	<link>http://www.mdpi.com/2073-4433/3/1/1</link>
	<description>Gas-phase chemical mechanisms are vital components of prognostic air quality models. The mechanisms are incorporated into modules that are used to calculate the chemical sources and sinks of ozone and the precursors of particulates. Fifty years ago essential atmospheric chemical processes, such as the importance of the hydroxyl radical, were unknown and crude air quality models incorporated only a few parameterized reactions obtained by fitting observations. Over the years, chemical mechanisms for air quality modeling improved and became more detailed as more experimental data and more powerful computers became available. However it will not be possible to incorporate a detailed treatment of the chemistry for all known chemical constituents because there are thousands of organic compounds emitted into the atmosphere. Some simplified method of treating atmospheric organic chemistry is required to make air quality modeling computationally possible. The majority of the significant differences between air quality mechanisms are due to the differing methods of treating this organic chemistry. The purpose of this review is to present an overview of atmospheric chemistry that is incorporated into air quality mechanisms and to suggest areas in which more research is needed.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2011-12-21</prism:publicationDate>
	<prism:volume>3</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Review</prism:section>
	<prism:doi>10.3390/atmos3010001</prism:doi>
	<prism:startingPage>1</prism:startingPage>
		<prism:endingPage>32</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[A Review of Tropospheric Atmospheric Chemistry and Gas-Phase Chemical Mechanisms for Air Quality Modeling]]></dc:title>
    <dc:date>2011-12-21</dc:date>
	<dc:identifier>doi: 10.3390/atmos3010001</dc:identifier>
    	<dc:creator>William R. Stockwell</dc:creator>
		<dc:creator>Charlene V. Lawson</dc:creator>
		<dc:creator>Emily Saunders</dc:creator>
		<dc:creator>Wendy S. Goliff</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/2/4/715">
	<title><![CDATA[Atmosphere, Vol. 2, Pages 715-741: Case Study of Pollutants Concentration Sensitivity to Meteorological Fields and Land Use Parameters over Douala (Cameroon) Using AERMOD Dispersion Model]]></title>
	<link>http://www.mdpi.com/2073-4433/2/4/715</link>
	<description>This paper deals with the simulation of the NOx concentration over Douala for the period 2002–2006 by means of the American Meteorological Society (AMS)/Environmental Protection Agency (EPA) Regulatory Model (AERMOD) model, version 07026. Its sensitivity to local meteorological fields and land use parameters are investigated by selecting different buildings (receptors) specific direction and distance from the source and by making changes in land use parameters. Results reveal variations in concentration patterns depending on the roughness length, albedo and the Bowen ratio. Changes in the albedo as well as the Bowen ratio only alter the concentration patterns during convective conditions. For a short averaging time, changes in albedo and Bowen ratio have the same effects on the concentration patterns. These results not only help to accurately choose the indicated areas for implanting industrial sites, to manage risk assessment exposure to pollutants in Douala city and addressing recommendations to policies makers.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2011-12-14</prism:publicationDate>
	<prism:volume>2</prism:volume>
	<prism:number>4</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos2040715</prism:doi>
	<prism:startingPage>715</prism:startingPage>
		<prism:endingPage>741</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Case Study of Pollutants Concentration Sensitivity to Meteorological Fields and Land Use Parameters over Douala (Cameroon) Using AERMOD Dispersion Model]]></dc:title>
    <dc:date>2011-12-14</dc:date>
	<dc:identifier>doi: 10.3390/atmos2040715</dc:identifier>
    	<dc:creator>Pascal Moudi Igri</dc:creator>
		<dc:creator>Derbetini Appolinaire Vondou</dc:creator>
		<dc:creator>François Mkankam Kamga</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/2/4/702">
	<title><![CDATA[Atmosphere, Vol. 2, Pages 702-714: Carbon Dioxide and Methane at a Desert Site—A Case Study at Railroad Valley Playa, Nevada, USA]]></title>
	<link>http://www.mdpi.com/2073-4433/2/4/702</link>
	<description>Ground based in-situ measurements of carbon dioxide (CO2) and methane (CH4) at the dry lakebed at Railroad Valley (RRV) playa, Nevada, USA (38°30.234′ N, 115°41.604′ W, elevation 1437 m) were conducted over a five day period from 20–25 June 2010. The playa is a flat, desert site with virtually no vegetation, an overall size of 15 km × 15 km and is approximately 110 km south-west of the nearest city, Ely (elevation 1962 m, inhabitants 4000). The measurements were taken in support of the vicarious calibration experiment to validate column-averaged dry air mole fractions of CO2 and CH4 (XCO2 and XCH4) retrieved from the Greenhouse Gases Observing Satellite (GOSAT) which was launched in January 2009. This work reports on ground-based in-situ measurements of CO2 and CH4 from RRV playa and describes comparisons made between in-situ data and XCO2 and XCH4 from GOSAT.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2011-12-08</prism:publicationDate>
	<prism:volume>2</prism:volume>
	<prism:number>4</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos2040702</prism:doi>
	<prism:startingPage>702</prism:startingPage>
		<prism:endingPage>714</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Carbon Dioxide and Methane at a Desert Site—A Case Study at Railroad Valley Playa, Nevada, USA]]></dc:title>
    <dc:date>2011-12-08</dc:date>
	<dc:identifier>doi: 10.3390/atmos2040702</dc:identifier>
    	<dc:creator>Emma L. Yates</dc:creator>
		<dc:creator>Kathleen Schiro</dc:creator>
		<dc:creator>Max Lowenstein</dc:creator>
		<dc:creator>Edwin J. Sheffner</dc:creator>
		<dc:creator>Laura T. Iraci</dc:creator>
		<dc:creator>Jovan M. Tadić</dc:creator>
		<dc:creator>Akihiko Kuze</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/2/4/688">
	<title><![CDATA[Atmosphere, Vol. 2, Pages 688-701: A Comparison of Risk Estimates for the Effect of Short-Term Exposure to PM, NO2 and CO on Cardiovascular Hospitalizations and Emergency Department Visits: Effect Size Modeling of Study Findings]]></title>
	<link>http://www.mdpi.com/2073-4433/2/4/688</link>
	<description>Although particulate matter (PM), nitrogen dioxide (NO2) and carbon monoxide (CO) typically exist as part of a complex air pollution mixture, the evidence linking these pollutants to health effects is evaluated separately in the scientific and policy reviews of the National Ambient Air Quality Standards (NAAQS). The objective of this analysis was to use meta-regression methods to model effect estimates for several individual yet correlated NAAQS pollutants in an effort to identify factors that explain differences in the effect sizes across studies and across pollutants. We expected that our consideration of the evidence for several correlated pollutants in parallel could lead to insights regarding exposure to the pollutant mixture. We focused on studies of hospital admissions for congestive heart failure (CHF) and ischemic heart disease (IHD), which have played an important role in the evaluation of the scientific evidence communicated in the PM, NO2, and CO Integrated Science Assessments (ISAs). Of the studies evaluated, 11 CHF studies and 21 IHD studies met our inclusion requirements. The size of the risk estimates was explained by factors related to the pollution mixture, study methods, and monitoring network characteristics. Our findings suggest that additional analyses focusing on understanding differences in effect sizes across geographic areas with different pollution mixtures and monitor network designs may improve our understanding of the independent and combined effects of correlated pollutants.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2011-12-06</prism:publicationDate>
	<prism:volume>2</prism:volume>
	<prism:number>4</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos2040688</prism:doi>
	<prism:startingPage>688</prism:startingPage>
		<prism:endingPage>701</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[A Comparison of Risk Estimates for the Effect of Short-Term Exposure to PM, NO2 and CO on Cardiovascular Hospitalizations and Emergency Department Visits: Effect Size Modeling of Study Findings]]></dc:title>
    <dc:date>2011-12-06</dc:date>
	<dc:identifier>doi: 10.3390/atmos2040688</dc:identifier>
    	<dc:creator>Ellen Kirrane</dc:creator>
		<dc:creator>David Svendsgaard</dc:creator>
		<dc:creator>Mary Ross</dc:creator>
		<dc:creator>Barbara Buckley</dc:creator>
		<dc:creator>Allen Davis</dc:creator>
		<dc:creator>Doug Johns</dc:creator>
		<dc:creator>Dennis Kotchmar</dc:creator>
		<dc:creator>Thomas C. Long</dc:creator>
		<dc:creator>Thomas J. Luben</dc:creator>
		<dc:creator>Genee Smith</dc:creator>
		<dc:creator>Lindsay Wichers Stanek</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/2/4/671">
	<title><![CDATA[Atmosphere, Vol. 2, Pages 671-687: Desorption of Herbicides from Atmospheric Particulates During High-Volume Air Sampling]]></title>
	<link>http://www.mdpi.com/2073-4433/2/4/671</link>
	<description>Pesticides can be present in the atmosphere either as vapours and/or in association with suspended particles. High-volume air sampling, in which air is aspirated first through a glass fibre filter to capture pesticides associated with atmospheric particulates and then polyurethane foam (PUF), often in combination with an adsorbent resin such as XAD-2, to capture pesticides present as vapours, is generally employed during atmospheric monitoring for pesticides. However, the particulate fraction may be underestimated because some pesticides may be stripped or desorbed from captured particulates due to the pressure drop created by the high flow of air through the filter. This possibility was investigated with ten herbicide active ingredients commonly used on the Canadian prairies (dimethylamine salts of 2,4-D, MCPA and dicamba, 2,4-D 2-ethylhexyl ester, bromoxynil octanoate, diclofop methyl ester, fenoxaprop ethyl ester, trifluralin, triallate and ethalfluralin) and seven hydrolysis products (2,4-D, MCPA, dicamba, bromoxynil, diclofop, clopyralid and mecoprop). Finely ground heavy clay soil fortified with active ingredients/hydrolysis products was evenly distributed on the glass fibre filters of high-volume air samplers and air aspirated through the samplers at a flow rate of 12.5 m3/h for a 7-day period. The proportion desorbed as vapour from the fortified soil was determined by analysis of the PUF/XAD-2 resin composite cartridges. The extent of desorption from the fortified soil applied to the filters varied from 0% for each of the dimethylamine salts of 2,4-D, MCPA and dicamba to approximately 50% for trifluralin, triallate and ethalfluralin.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2011-11-14</prism:publicationDate>
	<prism:volume>2</prism:volume>
	<prism:number>4</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos2040671</prism:doi>
	<prism:startingPage>671</prism:startingPage>
		<prism:endingPage>687</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Desorption of Herbicides from Atmospheric Particulates During High-Volume Air Sampling]]></dc:title>
    <dc:date>2011-11-14</dc:date>
	<dc:identifier>doi: 10.3390/atmos2040671</dc:identifier>
    	<dc:creator>Allan J. Cessna</dc:creator>
		<dc:creator>Don T. Waite</dc:creator>
		<dc:creator>Jonathan Bailey</dc:creator>
		<dc:creator>Lorne A. Kerr</dc:creator>
		<dc:creator>Dwight V. Quiring</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/2/4/655">
	<title><![CDATA[Atmosphere, Vol. 2, Pages 655-670: Influence of Reduced Nitrogen Diets on Ammonia Emissions from Cattle Feedlot Pens]]></title>
	<link>http://www.mdpi.com/2073-4433/2/4/655</link>
	<description>Reducing crude protein (CP) in livestock diets may lower ammonia emissions. A feeding trial was conducted with crossbred steers at the Southeast Colorado Research Center in Lamar, Colorado from December 2009 to March 2010. Three diet treatments were investigated: Reduced (11.6% CP), Oscillating (13.5% crude protein 4 days/week and 11.6% CP 3 days/week) and Control (13.5% CP). Intact soil core samples (n = 36 per sampling date) were collected from the pen surfaces on three dates corresponding to 45, 92, and 148 days into the feeding cycle. Four pens from each diet treatment were sampled. Cores were placed into flow-through laboratory chambers for seven days and ammonia fluxes were trapped in acid bubblers that were refreshed every 24 h. Average daily ammonia emissions for the Control diet ranged from 6.6 to 9.4 g NH3 m−2·day−1; average daily emission for the Oscillating diet ranged from 6.3 to 8.8 g NH3 m−2·day−1; and average daily flux for the Reduced diet ranged from 4.1 to 5.8 g NH3 m−2·day−1. Ammonia fluxes from the reduced N treatment were significantly lower (21% to 40%) than from the control diet on the first two sample dates. There was no significant difference between the Oscillating and Control treatments. Reducing CP in cattle feedlot diets may be an effective method for reducing ammonia emissions from pen surfaces. More research is needed to validate these results at commercial scales in different environments to determine if reductions in ammonia can be sustained with lower CP diets without affecting rate of gain, feed efficiency and health.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2011-11-11</prism:publicationDate>
	<prism:volume>2</prism:volume>
	<prism:number>4</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos2040655</prism:doi>
	<prism:startingPage>655</prism:startingPage>
		<prism:endingPage>670</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Influence of Reduced Nitrogen Diets on Ammonia Emissions from Cattle Feedlot Pens]]></dc:title>
    <dc:date>2011-11-11</dc:date>
	<dc:identifier>doi: 10.3390/atmos2040655</dc:identifier>
    	<dc:creator>Karen Galles</dc:creator>
		<dc:creator>Jay Ham</dc:creator>
		<dc:creator>Elin Westover</dc:creator>
		<dc:creator>Joshua Stratton</dc:creator>
		<dc:creator>John Wagner</dc:creator>
		<dc:creator>Terry Engle</dc:creator>
		<dc:creator>Tony C. Bryant</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/2/4/633">
	<title><![CDATA[Atmosphere, Vol. 2, Pages 633-654: Emission Ratios for Ammonia and Formic Acid and Observations of Peroxy Acetyl Nitrate (PAN) and Ethylene in Biomass Burning Smoke as Seen by the Tropospheric Emission Spectrometer (TES)]]></title>
	<link>http://www.mdpi.com/2073-4433/2/4/633</link>
	<description>We use the Tropospheric Emission Spectrometer (TES) aboard the NASA Aura satellite to determine the concentrations of the trace gases ammonia (NH3) and formic acid (HCOOH) within boreal biomass burning plumes, and present the first detection of peroxy acetyl nitrate (PAN) and ethylene (C2H4) by TES. We focus on two fresh Canadian plumes observed by TES in the summer of 2008 as part of the Arctic Research of the Composition of the Troposphere from Aircraft and Satellites (ARCTAS-B) campaign. We use TES retrievals of NH3 and HCOOH within the smoke plumes to calculate their emission ratios (1.0% ± 0.5% and 0.31% ± 0.21%, respectively) relative to CO for these Canadian fires. The TES derived emission ratios for these gases agree well with previous aircraft and satellite estimates, and can complement ground-based studies that have greater surface sensitivity. We find that TES observes PAN mixing ratios of ~2 ppb within these mid-tropospheric boreal biomass burning plumes when the average cloud optical depth is low ( &amp;lt; 0.1) and that TES can detect C2H4 mixing ratios of ~2 ppb in fresh biomass burning smoke plumes.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2011-11-09</prism:publicationDate>
	<prism:volume>2</prism:volume>
	<prism:number>4</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos2040633</prism:doi>
	<prism:startingPage>633</prism:startingPage>
		<prism:endingPage>654</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Emission Ratios for Ammonia and Formic Acid and Observations of Peroxy Acetyl Nitrate (PAN) and Ethylene in Biomass Burning Smoke as Seen by the Tropospheric Emission Spectrometer (TES)]]></dc:title>
    <dc:date>2011-11-09</dc:date>
	<dc:identifier>doi: 10.3390/atmos2040633</dc:identifier>
    	<dc:creator>Matthew J. Alvarado</dc:creator>
		<dc:creator>Karen E. Cady-Pereira</dc:creator>
		<dc:creator>Yaping Xiao</dc:creator>
		<dc:creator>Dylan B. Millet</dc:creator>
		<dc:creator>Vivienne H. Payne</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/2/4/617">
	<title><![CDATA[Atmosphere, Vol. 2, Pages 617-632: Emission Ratios of the Tropospheric Ozone Precursors Nitrogen Dioxide and Formaldehyde from Australia’s Black Saturday Fires]]></title>
	<link>http://www.mdpi.com/2073-4433/2/4/617</link>
	<description>The ‘Black Saturday’ fires were a series of devastating forest fires that burned across Victoria, Australia, during February and March of 2009. In this study we have used satellite data made publically available by NASA from the Ozone Monitoring Instrument (OMI) and the Atmospheric InfraRed Sounder (AIRS) to track the smoke plume from the Black Saturday firestorm and explore the chemical aging of the smoke plume in the first days after emission. We also determined emission ratios for formaldehyde and nitrogen dioxide within smoke from fires actively burning across Victoria between 7 and 17 February 2009. The mean emission ratios with respect to carbon monoxide derived for these two tropospheric ozone precursors are (0.016 ± 0.004 mol.mol−1) for formaldehyde and (0.005 ± 0.002 mol.mol−1) for nitrogen dioxide. The mean emission ratio for formaldehyde with respect to CO is in broad agreement with values previously quoted in the literature for temperate forest fires. However, to our knowledge there are no previous measurements of emission ratios for nitrogen dioxide from Australian temperate forest fires.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2011-10-31</prism:publicationDate>
	<prism:volume>2</prism:volume>
	<prism:number>4</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos2040617</prism:doi>
	<prism:startingPage>617</prism:startingPage>
		<prism:endingPage>632</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Emission Ratios of the Tropospheric Ozone Precursors Nitrogen Dioxide and Formaldehyde from Australia’s Black Saturday Fires]]></dc:title>
    <dc:date>2011-10-31</dc:date>
	<dc:identifier>doi: 10.3390/atmos2040617</dc:identifier>
    	<dc:creator>Emma Young</dc:creator>
		<dc:creator>Clare Paton-Walsh</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/2/4/567">
	<title><![CDATA[Atmosphere, Vol. 2, Pages 567-616: Cloud Processing of Gases and Aerosols in Air Quality Modeling]]></title>
	<link>http://www.mdpi.com/2073-4433/2/4/567</link>
	<description>The representations of cloud processing of gases and aerosols in some of the current state-of-the-art regional air quality models in North America and Europe are reviewed. Key processes reviewed include aerosol activation (or nucleation scavenging of aerosols), aqueous-phase chemistry, and wet deposition/removal of atmospheric tracers. It was found that models vary considerably in the parameterizations or algorithms used in representing these processes. As an emerging area of research, the current understanding of the uptake of water soluble organics by cloud droplets and the potential aqueous-phase reaction pathways leading to the atmospheric secondary organic aerosol (SOA) formation is also reviewed. Sensitivity tests using the AURAMS model have been conducted in order to assess the impact on modeled regional particulate matter (PM) from: (1) the different aerosol activation schemes, (2) the different below-cloud particle scavenging algorithms, and (3) the inclusion of cloud processing of water soluble organics as a potential pathway for the formation of atmospheric SOA. It was found that the modeled droplet number concentrations and ambient PM size distributions were strongly affected by the use of different aerosol activation schemes. The impact on the modeled average ambient PM mass concentration was found to be limited in terms of averaged PM2.5 concentration (~a few percents) but more significant in terms of PM1.0 (up to 10 percents). The modeled ambient PM was found to be moderately sensitive to the below-cloud particle scavenging algorithms, with relative differences up to 10% and 20% in terms of PM2.5 and PM10, respectively, when using the two different algorithms for the scavenging coefficient (Λ) corresponding to the lower and upper bounds in the parameterization for Λ. The model simulation with the additional cloud uptake and processing of water-soluble organic gases was shown to improve the evaluation statistics for modeled PM2.5 OA compared to the IMPROVE network data, and it was demonstrated that the cloud processing of water-soluble organics can indeed be an important mechanism in addition to the traditional secondary organic gas uptake to the particle organic phase.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2011-10-10</prism:publicationDate>
	<prism:volume>2</prism:volume>
	<prism:number>4</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos2040567</prism:doi>
	<prism:startingPage>567</prism:startingPage>
		<prism:endingPage>616</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Cloud Processing of Gases and Aerosols in Air Quality Modeling]]></dc:title>
    <dc:date>2011-10-10</dc:date>
	<dc:identifier>doi: 10.3390/atmos2040567</dc:identifier>
    	<dc:creator>Wanmin Gong</dc:creator>
		<dc:creator>Craig Stroud</dc:creator>
		<dc:creator>Leiming Zhang</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/2/3/553">
	<title><![CDATA[Atmosphere, Vol. 2, Pages 553-566: Measuring Trace Gas Emission from Multi-Distributed Sources Using Vertical Radial Plume Mapping (VRPM) and Backward Lagrangian Stochastic (bLS) Techniques]]></title>
	<link>http://www.mdpi.com/2073-4433/2/3/553</link>
	<description>Two micrometeorological techniques for measuring trace gas emission rates from distributed area sources were evaluated using a variety of synthetic area sources. The vertical radial plume mapping (VRPM) and the backward Lagrangian stochastic (bLS) techniques with an open-path optical spectroscopic sensor were evaluated for relative accuracy for multiple emission-source and sensor configurations. The relative accuracy was calculated by dividing the measured emission rate by the actual emission rate; thus, a relative accuracy of 1.0 represents a perfect measure. For a single area emission source, the VRPM technique yielded a somewhat high relative accuracy of 1.38 ± 0.28. The bLS technique resulted in a relative accuracy close to unity, 0.98 ± 0.24. Relative accuracies for dual source emissions for the VRPM and bLS techniques were somewhat similar to single source emissions, 1.23 ± 0.17 and 0.94 ± 0.24, respectively. When the bLS technique was used with vertical point concentrations, the relative accuracy was unacceptably low.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2011-09-23</prism:publicationDate>
	<prism:volume>2</prism:volume>
	<prism:number>3</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos2030553</prism:doi>
	<prism:startingPage>553</prism:startingPage>
		<prism:endingPage>566</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Measuring Trace Gas Emission from Multi-Distributed Sources Using Vertical Radial Plume Mapping (VRPM) and Backward Lagrangian Stochastic (bLS) Techniques]]></dc:title>
    <dc:date>2011-09-23</dc:date>
	<dc:identifier>doi: 10.3390/atmos2030553</dc:identifier>
    	<dc:creator>Kyoung S. Ro</dc:creator>
		<dc:creator>Melvin H. Johnson</dc:creator>
		<dc:creator>Patrick G. Hunt</dc:creator>
		<dc:creator>Thomas K. Flesch</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/2/3/533">
	<title><![CDATA[Atmosphere, Vol. 2, Pages 533-552: Seasonal Gradient Patterns of Polycyclic Aromatic Hydrocarbons and Particulate Matter Concentrations near a Highway]]></title>
	<link>http://www.mdpi.com/2073-4433/2/3/533</link>
	<description>Close proximity to roadways has been associated with higher exposure to traffic-related air pollutants. However, analyses of the effects of season and meteorological parameters on horizontal gradient patterns of traffic-generated air pollutants still need to be elucidated. Our objectives were to: (1) determine effects of season on horizontal gradient patterns of polycyclic aromatic hydrocarbons (PAHs), total suspended particles (TSP), and PM2.5 near a heavily trafficked highway; and (2) examine the effect of day-of-the-week variations (weekday versus weekend) associated with traffic counts on measured airborne-contaminant levels. PAHs (Σ8PAHs [MW 228–278]; gas + particulate), TSP and PM2.5 were monitored at nominal distances (50, 100, and 150 m) from the New Jersey Turnpike every 6 days for periods of 24 h, between September 2007 and September 2008. Seasonal variations in the horizontal gradient patterns of Σ8PAHs were observed. In the summer, Σ8PAHs declined significantly between 50–100 m from the highway (23% decrease), but not between the furthermost distances (100–150 m). An inverse pattern was observed in the winter: Σ8PAHs declined between 100–150 m (26% decrease), but not between the closest distances. Σ8PAHs and TSP, but not PM2.5, concentrations measured on weekends were 12–37% lower than those on weekdays, respectively, corresponding to lower diesel traffic volume. This study suggests that people living in the close proximity to highways may be exposed to varying levels of Σ8PAHs, TSP, and PM2.5 depending on distance to highway, season, and day-of-the-week variations.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2011-09-21</prism:publicationDate>
	<prism:volume>2</prism:volume>
	<prism:number>3</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos2030533</prism:doi>
	<prism:startingPage>533</prism:startingPage>
		<prism:endingPage>552</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Seasonal Gradient Patterns of Polycyclic Aromatic Hydrocarbons and Particulate Matter Concentrations near a Highway]]></dc:title>
    <dc:date>2011-09-21</dc:date>
	<dc:identifier>doi: 10.3390/atmos2030533</dc:identifier>
    	<dc:creator>Kyung Hwa Jung</dc:creator>
		<dc:creator>Francisco Artigas</dc:creator>
		<dc:creator>Jin Y. Shin</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/2/3/510">
	<title><![CDATA[Atmosphere, Vol. 2, Pages 510-532: Chemical Mechanism Solvers in Air Quality Models]]></title>
	<link>http://www.mdpi.com/2073-4433/2/3/510</link>
	<description>The solution of chemical kinetics is one of the most computationally intensivetasks in atmospheric chemical transport simulations. Due to the stiff nature of the system,implicit time stepping algorithms which repeatedly solve linear systems of equations arenecessary. This paper reviews the issues and challenges associated with the construction ofefficient chemical solvers, discusses several families of algorithms, presents strategies forincreasing computational efficiency, and gives insight into implementing chemical solverson accelerated computer architectures.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2011-09-13</prism:publicationDate>
	<prism:volume>2</prism:volume>
	<prism:number>3</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos2030510</prism:doi>
	<prism:startingPage>510</prism:startingPage>
		<prism:endingPage>532</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Chemical Mechanism Solvers in Air Quality Models]]></dc:title>
    <dc:date>2011-09-13</dc:date>
	<dc:identifier>doi: 10.3390/atmos2030510</dc:identifier>
    	<dc:creator>Hong Zhang</dc:creator>
		<dc:creator>John C. Linford</dc:creator>
		<dc:creator>Adrian Sandu</dc:creator>
		<dc:creator>Rolf Sander</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/2/3/484">
	<title><![CDATA[Atmosphere, Vol. 2, Pages 484-509: Adaptive Grid Use in Air Quality Modeling]]></title>
	<link>http://www.mdpi.com/2073-4433/2/3/484</link>
	<description>The predictions from air quality models are subject to many sources of uncertainty; among them, grid resolution has been viewed as one that is limited by the availability of computational resources. A large grid size can lead to unacceptable errors for many pollutants formed via nonlinear chemical reactions. Further, insufficient grid resolution limits the ability to perform accurate exposure assessments. To address this issue in parallel to increasing computational power, modeling techniques that apply finer grids to areas of interest and coarser grids elsewhere have been developed. Techniques using multiple grid sizes are called nested grid or multiscale modeling techniques. These approaches are limited by uncertainty in the placement of finer grids since pertinent locations may not be known a priori, loss in solution accuracy due to grid boundary interface problems, and inability to adjust to changes in grid resolution requirements. A different approach to achieve local resolution involves using dynamic adaptive grids. Various adaptive mesh refinement techniques using structured grids as well as mesh enrichment techniques on unstructured grids have been explored in atmospheric modeling. Recently, some of these techniques have been applied to full blown air quality models. In this paper, adaptive grid methods used in air quality modeling are reviewed and categorized. The advantages and disadvantages of each adaptive grid method are discussed. Recent advances made in air quality simulation owing to the use of adaptive grids are summarized. Relevant connections to adaptive grid modeling in weather and climate modeling are also described.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2011-09-09</prism:publicationDate>
	<prism:volume>2</prism:volume>
	<prism:number>3</prism:number>
	<prism:section>Review</prism:section>
	<prism:doi>10.3390/atmos2030484</prism:doi>
	<prism:startingPage>484</prism:startingPage>
		<prism:endingPage>509</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Adaptive Grid Use in Air Quality Modeling]]></dc:title>
    <dc:date>2011-09-09</dc:date>
	<dc:identifier>doi: 10.3390/atmos2030484</dc:identifier>
    	<dc:creator>Fernando Garcia-Menendez</dc:creator>
		<dc:creator>Mehmet Talat Odman</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/2/3/464">
	<title><![CDATA[Atmosphere, Vol. 2, Pages 464-483: Coupling of Important Physical Processes in the Planetary Boundary Layer between Meteorological and Chemistry Models for Regional to Continental Scale Air Quality Forecasting: An Overview]]></title>
	<link>http://www.mdpi.com/2073-4433/2/3/464</link>
	<description>A consensus among many Air Quality (AQ) modelers is that planetary boundary layer processes are the most influential processes for surface concentrations of air pollutants. Due to the many uncertainties intrinsically embedded in the parameterization of these processes, parameter optimization is often employed to determine an optimal set or range of values of the sensitive parameters. In this review study, we focus on the two of the most important physical processes: turbulent mixing and dry deposition. An emphasis was put on surveying AQ models that have been proven to resolve meso-scale features and cover a large geographical area, such as large regional, continental, or trans-continental boundary extents. Five AQ models were selected. Four of the models were run in real-time operational forecasting settings for continental scale AQ. The models use various forms of level 2.5 closure algorithms to calculate turbulent mixing. Tuning and parameter optimization has been used to tailor these algorithms to better suit their AQ models which are typically comprised of a coupled chemistry and meteorology model. Longer forecasts and long lead-times are inevitably under increasing demand for these models. Land Surface Models that have the capability for soil moisture and temperature data assimilation will have an advantage to constrain the key variables that govern the partitioning of surface sensible and latent heat fluxes and thus attain the potential to perform better in longer forecasts than those models that do not have this capability. Dry deposition velocity is a very significant model parameter that governs a major surface exchange activity. An exploratory study has been conducted to see the upper bound of roughness length in the similarity equation for aerodynamic resistance.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2011-08-31</prism:publicationDate>
	<prism:volume>2</prism:volume>
	<prism:number>3</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos2030464</prism:doi>
	<prism:startingPage>464</prism:startingPage>
		<prism:endingPage>483</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Coupling of Important Physical Processes in the Planetary Boundary Layer between Meteorological and Chemistry Models for Regional to Continental Scale Air Quality Forecasting: An Overview]]></dc:title>
    <dc:date>2011-08-31</dc:date>
	<dc:identifier>doi: 10.3390/atmos2030464</dc:identifier>
    	<dc:creator>Pius Lee</dc:creator>
		<dc:creator>Fong Ngan</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/2/3/426">
	<title><![CDATA[Atmosphere, Vol. 2, Pages 426-463: Chemical Data Assimilation—An Overview]]></title>
	<link>http://www.mdpi.com/2073-4433/2/3/426</link>
	<description>Chemical data assimilation is the process by which models use measurements to produce an optimal representation of the chemical composition of the atmosphere. Leveraging advances in algorithms and increases in the available computational power, the integration of numerical predictions and observations has started to play an important role in air quality modeling. This paper gives an overview of several methodologies used in chemical data assimilation. We discuss the Bayesian framework for developing data assimilation systems, the suboptimal and the ensemble Kalman filter approaches, the optimal interpolation (OI), and the three and four dimensional variational methods. Examples of assimilation real observations with CMAQ model are presented.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2011-08-29</prism:publicationDate>
	<prism:volume>2</prism:volume>
	<prism:number>3</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos2030426</prism:doi>
	<prism:startingPage>426</prism:startingPage>
		<prism:endingPage>463</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Chemical Data Assimilation—An Overview]]></dc:title>
    <dc:date>2011-08-29</dc:date>
	<dc:identifier>doi: 10.3390/atmos2030426</dc:identifier>
    	<dc:creator>Adrian Sandu</dc:creator>
		<dc:creator>Tianfeng Chai</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/2/3/407">
	<title><![CDATA[Atmosphere, Vol. 2, Pages 407-425: Air Quality Response Modeling for Decision Support]]></title>
	<link>http://www.mdpi.com/2073-4433/2/3/407</link>
	<description>Air quality management relies on photochemical models to predict the responses of pollutant concentrations to changes in emissions. Such modeling is especially important for secondary pollutants such as ozone and fine particulate matter which vary nonlinearly with changes in emissions. Numerous techniques for probing pollutant-emission relationships within photochemical models have been developed and deployed for a variety of decision support applications. However, atmospheric response modeling remains complicated by the challenge of validating sensitivity results against observable data. This manuscript reviews the state of the science of atmospheric response modeling as well as efforts to characterize the accuracy and uncertainty of sensitivity results.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2011-08-26</prism:publicationDate>
	<prism:volume>2</prism:volume>
	<prism:number>3</prism:number>
	<prism:section>Review</prism:section>
	<prism:doi>10.3390/atmos2030407</prism:doi>
	<prism:startingPage>407</prism:startingPage>
		<prism:endingPage>425</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Air Quality Response Modeling for Decision Support]]></dc:title>
    <dc:date>2011-08-26</dc:date>
	<dc:identifier>doi: 10.3390/atmos2030407</dc:identifier>
    	<dc:creator>Daniel S. Cohan</dc:creator>
		<dc:creator>Sergey L. Napelenok</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/2/3/389">
	<title><![CDATA[Atmosphere, Vol. 2, Pages 389-406: Sub-Grid Scale Plume Modeling]]></title>
	<link>http://www.mdpi.com/2073-4433/2/3/389</link>
	<description>Multi-pollutant chemical transport models (CTMs) are being routinely used to predict the impacts of emission controls on the concentrations and deposition of primary and secondary pollutants. While these models have a fairly comprehensive treatment of the governing atmospheric processes, they are unable to correctly represent processes that occur at very fine scales, such as the near-source transport and chemistry of emissions from elevated point sources, because of their relatively coarse horizontal resolution. Several different approaches have been used to address this limitation, such as using fine grids, adaptive grids, hybrid modeling, or an embedded sub-grid scale plume model, i.e., plume-in-grid (PinG) modeling. In this paper, we first discuss the relative merits of these various approaches used to resolve sub-grid scale effects in grid models, and then focus on PinG modeling which has been very effective in addressing the problems listed above. We start with a history and review of PinG modeling from its initial applications for ozone modeling in the Urban Airshed Model (UAM) in the early 1980s using a relatively simple plume model, to more sophisticated and state-of-the-science plume models, that include a full treatment of gas-phase, aerosol, and cloud chemistry, embedded in contemporary models such as CMAQ, CAMx, and WRF-Chem. We present examples of some typical results from PinG modeling for a variety of applications, discuss the implications of PinG on model predictions of source attribution, and discuss possible future developments and applications for PinG modeling.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2011-08-24</prism:publicationDate>
	<prism:volume>2</prism:volume>
	<prism:number>3</prism:number>
	<prism:section>Review</prism:section>
	<prism:doi>10.3390/atmos2030389</prism:doi>
	<prism:startingPage>389</prism:startingPage>
		<prism:endingPage>406</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Sub-Grid Scale Plume Modeling]]></dc:title>
    <dc:date>2011-08-24</dc:date>
	<dc:identifier>doi: 10.3390/atmos2030389</dc:identifier>
    	<dc:creator>Prakash Karamchandani</dc:creator>
		<dc:creator>Krish Vijayaraghavan</dc:creator>
		<dc:creator>Greg Yarwood</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/2/3/358">
	<title><![CDATA[Atmosphere, Vol. 2, Pages 358-388: Modeling Smoke Plume-Rise and Dispersion from Southern United States Prescribed Burns with Daysmoke]]></title>
	<link>http://www.mdpi.com/2073-4433/2/3/358</link>
	<description>We present Daysmoke, an empirical-statistical plume rise and dispersion model for simulating smoke from prescribed burns. Prescribed fires are characterized by complex plume structure including multiple-core updrafts which makes modeling with simple plume models difficult. Daysmoke accounts for plume structure in a three-dimensional veering/sheering atmospheric environment, multiple-core updrafts, and detrainment of particulate matter. The number of empirical coefficients appearing in the model theory is reduced through a sensitivity analysis with the Fourier Amplitude Sensitivity Test (FAST). Daysmoke simulations for “bent-over” plumes compare closely with Briggs theory although the two-thirds law is not explicit in Daysmoke. However, the solutions for the “highly-tilted” plume characterized by weak buoyancy, low initial vertical velocity, and large initial plume diameter depart considerably from Briggs theory. Results from a study of weak plumes from prescribed burns at Fort Benning GA showed simulated ground-level PM2.5 comparing favorably with observations taken within the first eight kilometers of eleven prescribed burns. Daysmoke placed plume tops near the lower end of the range of observed plume tops for six prescribed burns. Daysmoke provides the levels and amounts of smoke injected into regional scale air quality models. Results from CMAQ with and without an adaptive grid are presented.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2011-08-19</prism:publicationDate>
	<prism:volume>2</prism:volume>
	<prism:number>3</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos2030358</prism:doi>
	<prism:startingPage>358</prism:startingPage>
		<prism:endingPage>388</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Modeling Smoke Plume-Rise and Dispersion from Southern United States Prescribed Burns with Daysmoke]]></dc:title>
    <dc:date>2011-08-19</dc:date>
	<dc:identifier>doi: 10.3390/atmos2030358</dc:identifier>
    	<dc:creator>Gary L. Achtemeier</dc:creator>
		<dc:creator>Scott A. Goodrick</dc:creator>
		<dc:creator>Yongqiang Liu</dc:creator>
		<dc:creator>Fernando Garcia-Menendez</dc:creator>
		<dc:creator>Yongtao Hu</dc:creator>
		<dc:creator>Mehmet Talat Odman</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/2/3/330">
	<title><![CDATA[Atmosphere, Vol. 2, Pages 330-357: Climate Variability and Its Impact on Forest Hydrology on South Carolina Coastal Plain, USA]]></title>
	<link>http://www.mdpi.com/2073-4433/2/3/330</link>
	<description>Understanding the changes in hydrology of coastal forested wetlands induced by climate change is fundamental for developing strategies to sustain their functions and services. This study examined 60 years of climatic observations and 30 years of hydrological data, collected at the Santee Experimental Forest (SEF) in coastal South Carolina. We also applied a physically-based, distributed hydrological model (MIKE SHE) to better understand the hydrological responses to the observed climate variability. The results from both observation and simulation for the paired forested watershed systems indicated that the forest hydrology was highly susceptible to change due to climate change. The stream flow and water table depth was substantially altered with a change in precipitation. Both flow and water table level decreased with a rise in temperature. The results also showed that hurricanes substantially influenced the forest hydrological patterns for a short time period (several years) as a result of forest damage.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2011-08-16</prism:publicationDate>
	<prism:volume>2</prism:volume>
	<prism:number>3</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos2030330</prism:doi>
	<prism:startingPage>330</prism:startingPage>
		<prism:endingPage>357</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Climate Variability and Its Impact on Forest Hydrology on South Carolina Coastal Plain, USA]]></dc:title>
    <dc:date>2011-08-16</dc:date>
	<dc:identifier>doi: 10.3390/atmos2030330</dc:identifier>
    	<dc:creator>Zhaohua Dai</dc:creator>
		<dc:creator>Devendra M. Amatya</dc:creator>
		<dc:creator>Ge Sun</dc:creator>
		<dc:creator>Carl C. Trettin</dc:creator>
		<dc:creator>Changsheng Li</dc:creator>
		<dc:creator>Harbin Li</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/2/3/303">
	<title><![CDATA[Atmosphere, Vol. 2, Pages 303-329: Greenhouse Gas Emissions from Ground Level Area Sources in Dairy and Cattle Feedyard Operations]]></title>
	<link>http://www.mdpi.com/2073-4433/2/3/303</link>
	<description>A protocol that consisted of an isolation flux chamber and a portable gas chromatograph was used to directly quantify greenhouse gas (GHG) emissions at a dairy and a feedyard operation in the Texas Panhandle. Field sampling campaigns were performed 5 consecutive days only during daylight hours from 9:00 am to 7:00 pm each day. The objective of this research was to quantify and compare GHG emission rates (ERs) from ground level area sources (GLAS) at dairy and cattle feedyard operations during the summer. A total of 74 air samples using flux chamber were collected from the barn (manure lane and bedding area), loafing pen, open lot, settling basin, lagoons, and compost pile within the dairy operation. For the cattle feedyard, a total of 87 air samples were collected from four corner pens of a large feedlot, runoff holding pond, and compost pile. Three primary GHGs (methane, carbon dioxide, and nitrous oxide) were measured and quantified from both operations. The aggregate estimated ERs for CH4, CO2, and N2O were 836, 5573, 3.4 g hd−1 d−1 (collectively 27.5 kg carbon dioxide equivalent (CO2e) hd−1 d−1), respectively, at the dairy operation. The aggregate ERs for CH4, CO2, and N2O were 3.8, 1399, 0.68 g hd−1 d−1 (1.7 kg CO2e hd−1 d−1), respectively, from the feedyard. The estimated USEPA GHG ERs were about 13.2 and 1.16 kg CO2e hd−1 d−1, respectively, for dairy and feedyard operations. Aggregate CH4, CO2 and N2O ERs at the dairy facility were about 219, 4 and 5 times higher, respectively, than those at the feedyard. At the dairy, average CH4 ERs estimated from the settling basin, primary and secondary lagoons were significantly higher than those from the other GLAS, contributing about 98% of the aggregate CH4 emission. The runoff holding pond and pen surface of the feedyard contributed about 99% of the aggregate CH4 emission. Average CO2 and N2O ERs estimated from the pen surface area were significantly higher than those estimated from the compost pile and runoff pond. The pen surface alone contributed about 93% and 84% of the aggregate CO2 and N2O emission, respectively. Abatement and management practices that address GHG emissions from these sources will likely be most effective for reducing facility emissions.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2011-08-09</prism:publicationDate>
	<prism:volume>2</prism:volume>
	<prism:number>3</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos2030303</prism:doi>
	<prism:startingPage>303</prism:startingPage>
		<prism:endingPage>329</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Greenhouse Gas Emissions from Ground Level Area Sources in Dairy and Cattle Feedyard Operations]]></dc:title>
    <dc:date>2011-08-09</dc:date>
	<dc:identifier>doi: 10.3390/atmos2030303</dc:identifier>
    	<dc:creator>Md Saidul Borhan</dc:creator>
		<dc:creator>Sergio C. Capareda</dc:creator>
		<dc:creator>Saqib Mukhtar</dc:creator>
		<dc:creator>William B. Faulkner</dc:creator>
		<dc:creator>Russell McGee</dc:creator>
		<dc:creator>Calvin B. Parnell</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/2/3/271">
	<title><![CDATA[Atmosphere, Vol. 2, Pages 271-302: Surface Flux Modeling for Air Quality Applications]]></title>
	<link>http://www.mdpi.com/2073-4433/2/3/271</link>
	<description>For many gasses and aerosols, dry deposition is an important sink of atmospheric mass. Dry deposition fluxes are also important sources of pollutants to terrestrial and aquatic ecosystems. The surface fluxes of some gases, such as ammonia, mercury, and certain volatile organic compounds, can be upward into the air as well as downward to the surface and therefore should be modeled as bi-directional fluxes. Model parameterizations of dry deposition in air quality models have been represented by simple electrical resistance analogs for almost 30 years. Uncertainties in surface flux modeling in global to mesoscale models are being slowly reduced as more field measurements provide constraints on parameterizations. However, at the same time, more chemical species are being added to surface flux models as air quality models are expanded to include more complex chemistry and are being applied to a wider array of environmental issues. Since surface flux measurements of many of these chemicals are still lacking, resistances are usually parameterized using simple scaling by water or lipid solubility and reactivity. Advances in recent years have included bi-directional flux algorithms that require a shift from pre-computation of deposition velocities to fully integrated surface flux calculations within air quality models. Improved modeling of the stomatal component of chemical surface fluxes has resulted from improved evapotranspiration modeling in land surface models and closer integration between meteorology and air quality models. Satellite-derived land use characterization and vegetation products and indices are improving model representation of spatial and temporal variations in surface flux processes. This review describes the current state of chemical dry deposition modeling, recent progress in bi-directional flux modeling, synergistic model development research with field measurements, and coupling with meteorological land surface models.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2011-08-08</prism:publicationDate>
	<prism:volume>2</prism:volume>
	<prism:number>3</prism:number>
	<prism:section>Review</prism:section>
	<prism:doi>10.3390/atmos2030271</prism:doi>
	<prism:startingPage>271</prism:startingPage>
		<prism:endingPage>302</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Surface Flux Modeling for Air Quality Applications]]></dc:title>
    <dc:date>2011-08-08</dc:date>
	<dc:identifier>doi: 10.3390/atmos2030271</dc:identifier>
    	<dc:creator>Jonathan Pleim</dc:creator>
		<dc:creator>Limei Ran</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/2/3/256">
	<title><![CDATA[Atmosphere, Vol. 2, Pages 256-270: Nitrogen Isotope Fractionation and Origin of Ammonia Nitrogen Volatilized from Cattle Manure in Simulated Storage]]></title>
	<link>http://www.mdpi.com/2073-4433/2/3/256</link>
	<description>A series of laboratory experiments were conducted to establish the relationship between nitrogen (N) isotope composition of cattle manure and ammonia emissions, potential contribution of nitrogenous gases other than ammonia to manure N volatilization losses, and to determine the relative contribution of urinary- vs. fecal-N to ammonia emissions during the initial stage of manure storage. Data confirmed that ammonia volatilization losses from manure are most intensive during the first 2 to 3 days of storage and this coincides with a very rapid loss (hydrolysis) of urinary urea. Long-term (30 days) monitoring of δ15N of manure and emitted ammonia indicated that the dynamics of N isotope fractionation may be complicating the usefulness of the isotope approach as a tool for estimating ammonia emissions from manure in field conditions. The relationship between δ15N of manure and ammonia emission appears to be linear during the initial stages of manure storage (when most of the ammonia losses occur) and should be further investigated. These experiments demonstrated that the main source of ammonia-N volatilized from cattle manure during the initial 10 days of storage is urinary-N, representing on average 90% of the emitted ammonia-N. The contribution of fecal-N was relatively low, but gradually increased to about 10% by day 10. There appears to be substantial emissions of nitrogenous gases other than ammonia, most likely dinitrogen gas, which may account for up to 25% of N losses during the first 20 days of manure storage. This finding, which has to be confirmed in laboratory and field conditions, may be indicative of overestimation of ammonia emissions from cattle operations by the current emissions factors.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2011-08-02</prism:publicationDate>
	<prism:volume>2</prism:volume>
	<prism:number>3</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos2030256</prism:doi>
	<prism:startingPage>256</prism:startingPage>
		<prism:endingPage>270</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Nitrogen Isotope Fractionation and Origin of Ammonia Nitrogen Volatilized from Cattle Manure in Simulated Storage]]></dc:title>
    <dc:date>2011-08-02</dc:date>
	<dc:identifier>doi: 10.3390/atmos2030256</dc:identifier>
    	<dc:creator>Chanhee Lee</dc:creator>
		<dc:creator>Alexander N. Hristov</dc:creator>
		<dc:creator>Terri Cassidy</dc:creator>
		<dc:creator>Kyle Heyler</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/2/3/242">
	<title><![CDATA[Atmosphere, Vol. 2, Pages 242-255: Cross-Comparison of MODIS and CloudSat Data as a Tool to Validate Local Cloud Cover Masks]]></title>
	<link>http://www.mdpi.com/2073-4433/2/3/242</link>
	<description>This paper presents a cross-comparison of the data acquired by the MODIS and CloudSat sensors in order to understand the limit of the developed cloud-mask algorithm and to provide a quantitative validation assessment of cloud masks by using exclusively remotely sensed data. The analysis has been carried out by comparing both the intermediate levels of the cloud mask such as the brightness temperatures and the reflectance values for different channels, and the cloud mask itself with the cloud profiles as measured by the CloudSat sensor. The comparison between MODIS cloud tests and the CloudSat profiles indicates an agreement with hit rates (H) and Hanssen-Kuiper Skill Score (KSS) varying between 0.7 and 1.0 and 0.4 and 1.0, respectively. In this case, the low values of H and KSS are found due to the limitation of CloudSat to detect low clouds. The comparison between the cloud mask and the CloudSat profile determines H and KSS values between 0.6 and 1, except for one case. The CloudSat profile has also been compared with the Standard MODIS cloud mask in order to understand the improvement obtained in the use of local adapted thresholds. A comparison of MODIS and CALIPSO data is also presented.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2011-07-22</prism:publicationDate>
	<prism:volume>2</prism:volume>
	<prism:number>3</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos2030242</prism:doi>
	<prism:startingPage>242</prism:startingPage>
		<prism:endingPage>255</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Cross-Comparison of MODIS and CloudSat Data as a Tool to Validate Local Cloud Cover Masks]]></dc:title>
    <dc:date>2011-07-22</dc:date>
	<dc:identifier>doi: 10.3390/atmos2030242</dc:identifier>
    	<dc:creator>Claudia Notarnicola</dc:creator>
		<dc:creator>Daniela Di Rosa</dc:creator>
		<dc:creator>Francesco Posa</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/2/3/222">
	<title><![CDATA[Atmosphere, Vol. 2, Pages 222-241: The Coupled Effect of Mid-Tropospheric Moisture and Aerosol Abundance on Deep Convective Cloud Dynamics and Microphysics]]></title>
	<link>http://www.mdpi.com/2073-4433/2/3/222</link>
	<description>The humidity of the mid troposphere has a significant effect on the development of deep convection. Dry layers (dry intrusions) can inhibit deep convection through the effect of a thermal inversion resulting from radiation and due to the reduction in buoyancy resulting from entrainment. Recent observations have shown that the sensitivity of cloud top height to changes in mid-tropospheric humidity can be larger than straightforward “parcel dilution” would lead us to expect. Here, we investigate how aerosol effects on cloud development and microphysics are coupled to the effects of mid-tropospheric dry air. The two effects are coupled because the buoyancy loss through entrainment depends on droplet evaporation, so is controlled both by the environmental humidity and by droplet sizes, which are, in turn, controlled in part by the aerosol size distribution. Previous studies have not taken these microphysical effects into account. Cloud development and microphysics are examined using a 2-D non-hydrostatic cloud model with a detailed treatment of aerosol, drop, and ice-phase hydrometeor size spectra. A moderately deep mixed-phase convective cloud that developed over the High Plains of the United States is simulated. We find that a dry layer in the mid troposphere leads to a reduction in cloud updraft strength, droplet number, liquid water content and ice mass above the layer. The effect of the dry layer on these cloud properties is greatly enhanced under elevated aerosol conditions. In an environment with doubled aerosol number (but still realistic for continental conditions) the dry layer has about a three-times larger effect on cloud drop number and 50% greater effect on ice mass compared to an environment with lower aerosol. In the case with high aerosol loading, the dry layer stops convective development for over 10 min, and the maximum cloud top height reached is lower. However, the effect of the dry layer on cloud vertical development is significantly reduced when aerosol concentrations are lower. The coupled effect of mid-tropospheric dry air and aerosol on convective development is an additional way in which long term changes in aerosol may impact planetary cloud processes and climate.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2011-07-19</prism:publicationDate>
	<prism:volume>2</prism:volume>
	<prism:number>3</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos2030222</prism:doi>
	<prism:startingPage>222</prism:startingPage>
		<prism:endingPage>241</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[The Coupled Effect of Mid-Tropospheric Moisture and Aerosol Abundance on Deep Convective Cloud Dynamics and Microphysics]]></dc:title>
    <dc:date>2011-07-19</dc:date>
	<dc:identifier>doi: 10.3390/atmos2030222</dc:identifier>
    	<dc:creator>Zhiqiang Cui</dc:creator>
		<dc:creator>Kenneth S. Carslaw</dc:creator>
		<dc:creator>Alan M. Blyth</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/2/3/201">
	<title><![CDATA[Atmosphere, Vol. 2, Pages 201-221: Influence of Climatic Changes on Pollution Levels in Hungary and Surrounding Countries]]></title>
	<link>http://www.mdpi.com/2073-4433/2/3/201</link>
	<description>The influence of future climatic changes on some high pollution levels that can cause damage to plants and human beings is studied in this paper. The particular area of interest is Hungary and its surrounding countries. Three important quantities, which are closely related to ozone concentrations, have been investigated. We shall mainly focus on cases where the critical values, prescribed in the directives, are exceeded. Six scenarios, which allow us to compare directly the future and the present levels, have been run over a period of sixteen years. Some of the results obtained in the selected domain by using these scenarios have been carefully studied. The major conclusion is that an increase in temperature in combination with some other factors might lead to rather considerable increases of the damaging effects of ozone on plants and humans.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2011-07-18</prism:publicationDate>
	<prism:volume>2</prism:volume>
	<prism:number>3</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos2030201</prism:doi>
	<prism:startingPage>201</prism:startingPage>
		<prism:endingPage>221</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Influence of Climatic Changes on Pollution Levels in Hungary and Surrounding Countries]]></dc:title>
    <dc:date>2011-07-18</dc:date>
	<dc:identifier>doi: 10.3390/atmos2030201</dc:identifier>
    	<dc:creator>Zahari Zlatev</dc:creator>
		<dc:creator>Ágnes Havasi</dc:creator>
		<dc:creator>István Faragó</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/2/2/182">
	<title><![CDATA[Atmosphere, Vol. 2, Pages 182-200: Emissions from Ethanol-Gasoline Blends: A Single Particle Perspective]]></title>
	<link>http://www.mdpi.com/2073-4433/2/2/182</link>
	<description>Due to its agricultural origin and function as a fuel oxygenate, ethanol is being promoted as an alternative biomass-based fuel for use in spark ignition engines, with mandates for its use at state and regional levels. While it has been established that the addition of ethanol to a fuel reduces the particulate mass concentration in the exhaust, little attention has been paid to changes in the physicochemical properties of the emitted particles. In this work, a dynamometer-mounted GM Quad-4 spark ignition engine run without aftertreatment at 1,500 RPM and 100% load was used with four different fuel blends, containing 0, 20, 40 and 85 percent ethanol in gasoline. This allowed the effects of the fuel composition to be isolated from other effects. Instrumentation employed included two Aerosol Time-of-Flight Mass Spectrometers covering different size ranges for analysis of single particle composition, an Aethalometer for black carbon, a Scanning Mobility Particle Sizer for particle size distributions, a Photoelectric Aerosol Sensor for particle-bound polycyclic aromatic hydrocarbon (PAH) species and gravimetric filter measurements for particulate mass concentrations. It was found that, under the conditions investigated here, additional ethanol content in the fuel changes the particle size distribution, especially in the accumulation mode, and decreases the black carbon and total particulate mass concentrations. The molecular weight distribution of the PAHs was found to decrease with added ethanol. However, PAHs produced from higher ethanol-content fuels are associated with NO2− (m/z—46) in the single-particle mass spectra, indicating the presence of nitro-PAHs. Compounds associated with the gasoline (e.g., sulfur-containing species) are diminished due to dilution as ethanol is added to the fuel relative to those associated with the lubricating oil (e.g., calcium, zinc, phosphate) in the single particle spectra. These changes have potential implications for the health effect impacts of particulate emissions from biofuel blends.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2011-06-22</prism:publicationDate>
	<prism:volume>2</prism:volume>
	<prism:number>2</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos2020182</prism:doi>
	<prism:startingPage>182</prism:startingPage>
		<prism:endingPage>200</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Emissions from Ethanol-Gasoline Blends: A Single Particle Perspective]]></dc:title>
    <dc:date>2011-06-22</dc:date>
	<dc:identifier>doi: 10.3390/atmos2020182</dc:identifier>
    	<dc:creator>Dabrina D. Dutcher</dc:creator>
		<dc:creator>Mark R. Stolzenburg</dc:creator>
		<dc:creator>Samantha L. Thompson</dc:creator>
		<dc:creator>Juan M. Medrano</dc:creator>
		<dc:creator>Deborah S. Gross</dc:creator>
		<dc:creator>David B. Kittelson</dc:creator>
		<dc:creator>Peter H. McMurry</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/2/2/171">
	<title><![CDATA[Atmosphere, Vol. 2, Pages 171-181: No Borders for Tobacco Smoke in Hospitality Venues in Vienna]]></title>
	<link>http://www.mdpi.com/2073-4433/2/2/171</link>
	<description>In public places many countries banned smoking as the most important indoor source of fine airborne particulate matter. In Austria partial bans have been in force since 2009, with exemptions for the hospitality industry. From February to October 2010 we investigated PM2.5 concentrations in the breathing area of guests in well frequented Viennese establishments of all sizes, and compared these chance indoor samples with PM2.5 concentrations measured during the same half hour at the next outdoor monitoring station. The laser particle counter (OPC1.108, Grimm®) used for indoor measurements had been calibrated by ß-attenuation (FH 62 I-R, Eberline®), which was used outdoors. 48% of 112 venues visited did not fully comply with the law, notwithstanding its weakness.  Highest median concentrations (in µg/m3) were found in bars (443.7), followed by nightclubs/discotheques (421.1), pubs (147.7), cafes (106.1) and restaurants (23.4). Concentrations increased with number of smokers present (p &amp;lt; 0.01), with medians of 282.4/241,3/67.6/6.9 µg/m³ in smoking venues/smoking rooms/adjacent non-smoking rooms/exclusive non-smoking venues. Only for the latter, a significant correlation was found with outdoor concentrations (r = 0.48, p &amp;lt; 0.01), while concentrations in non-smoking rooms were higher (p &amp;lt; 0.01) and unrelated to outdoor concentrations, but significantly dependent on concentrations in the adjacent smoking room (r = 0.64, p &amp;lt; 0.01). In conclusion, the partial smoking ban failed and guests of Viennese hospitality venues continue to risk disease from passive smoking, even in so-called “non-smoking rooms”, which are second-hand smoke rooms.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2011-06-17</prism:publicationDate>
	<prism:volume>2</prism:volume>
	<prism:number>2</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos2020171</prism:doi>
	<prism:startingPage>171</prism:startingPage>
		<prism:endingPage>181</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[No Borders for Tobacco Smoke in Hospitality Venues in Vienna]]></dc:title>
    <dc:date>2011-06-17</dc:date>
	<dc:identifier>doi: 10.3390/atmos2020171</dc:identifier>
    	<dc:creator>Herbert Pletz</dc:creator>
		<dc:creator>Manfred Neuberger</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/2/2/146">
	<title><![CDATA[Atmosphere, Vol. 2, Pages 146-170: An Ensemble of Arctic Simulations of the AOE-2001 Field Experiment]]></title>
	<link>http://www.mdpi.com/2073-4433/2/2/146</link>
	<description>An ensemble of model runs with the COAMPS© regional model is compared to observations in the central Arctic for August 2001 from the Arctic Ocean Experiment 2001 (AOE-2001). The results are from a 6-km horizontal resolution 2nd, inner, nest of the model while the outermost model domain covers the pan-Arctic region, including the marginal ice zone and some of the land areas around the Arctic Ocean. Sea surface temperature and ice cover were prescribed from satellite data while sea-ice surface properties were modeled with an energy balance model, assuming a constant ice thickness. Five ensemble members were generated by altering the initialization time for the innermost nest, the surface roughness and the turbulent mixing scheme for clouds. The large size of the outer domain means that the model simulations have substantial deviations from the observations at synoptic-scale time scales. Therefore the evaluation focuses on statistical measures, rather than in details of individual ensemble member performance as compared directly to observations. In this context, the ensemble members are surprisingly similar even though details differ significantly. The ensemble average results features two main systematic problems: a consistent temperature bias, with too low temperatures below 2–3 km and slightly high temperatures through the rest of the troposphere, and a significant underestimation of the lowest clouds. In terms of total cloud cover, however, the model produces a realistic result; it is the very lowest clouds that are essentially missing. The temperature bias initially appears to be related to an interaction between clouds and radiation; the shape of the mean radiative heating-rate profile is very similar to that of the temperature bias. The lack of the lowest clouds could be due to the too low temperatures in conjunction with a cloud scheme that overestimates the transfer of cloud droplets to ice particles that precipitate. The different terms in the surface energy balance as well as the surface stress has only small systematic errors and are surprisingly consistent between the members.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2011-05-25</prism:publicationDate>
	<prism:volume>2</prism:volume>
	<prism:number>2</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos2020146</prism:doi>
	<prism:startingPage>146</prism:startingPage>
		<prism:endingPage>170</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[An Ensemble of Arctic Simulations of the AOE-2001 Field Experiment]]></dc:title>
    <dc:date>2011-05-25</dc:date>
	<dc:identifier>doi: 10.3390/atmos2020146</dc:identifier>
    	<dc:creator>Per Axelsson</dc:creator>
		<dc:creator>Michael Tjernström</dc:creator>
		<dc:creator>Stefan Söderberg</dc:creator>
		<dc:creator>Gunilla Svensson</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/2/2/129">
	<title><![CDATA[Atmosphere, Vol. 2, Pages 129-145: Climate Signals on the Regional Scale Derived with a Statistical Method: Relevance of the Driving Model’s Resolution]]></title>
	<link>http://www.mdpi.com/2073-4433/2/2/129</link>
	<description>When assessing the magnitude of climate signals in a regional scale, a host of optional approaches is feasible. This encompasses the use of regional climate models (RCM), nested into global climate models (GCM) for an area of interest as well as employing empirical statistical downscaling methods (ESD). In this context the question is addressed: Is an empirical statistical downscaling method capable of yielding results that are comparable to those by dynamical RCMs? Based on the presented ESD method, the comparison of RCM and ESD results show a high amount of agreement. In addition the empirical statistical downscaling can be applied directly to a GCM or a GCM-RCM cascade. The paper aims at comparing the consequences of employing various CGM-RCM-ESD combinations on the derived future changes of temperature and precipitation. This adds to the insight on the scale dependency of downscaling strategies. Results for one GCM with several scenario runs driving several RCMs with and without subsequent empirical statistical downscaling are presented. It is shown that there are only small differences between using the GCM results directly or as a GCM-RCM-ESD cascade.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2011-05-23</prism:publicationDate>
	<prism:volume>2</prism:volume>
	<prism:number>2</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos2020129</prism:doi>
	<prism:startingPage>129</prism:startingPage>
		<prism:endingPage>145</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Climate Signals on the Regional Scale Derived with a Statistical Method: Relevance of the Driving Model’s Resolution]]></dc:title>
    <dc:date>2011-05-23</dc:date>
	<dc:identifier>doi: 10.3390/atmos2020129</dc:identifier>
    	<dc:creator>Frank Kreienkamp</dc:creator>
		<dc:creator>Sonja Baumgart</dc:creator>
		<dc:creator>Arne Spekat</dc:creator>
		<dc:creator>Wolfgang Enke</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/2/2/110">
	<title><![CDATA[Atmosphere, Vol. 2, Pages 110-128: Improving Ammonia Emission Modeling and Inventories by Data Mining and Intelligent Interpretation of the National Air Emission Monitoring Study Database]]></title>
	<link>http://www.mdpi.com/2073-4433/2/2/110</link>
	<description>Ammonia emission is one of the greatest environmental concerns in sustainable agriculture development. Several limitations and fundamental problems associated with the current agricultural ammonia emission modeling and emission inventories have been identified. They were associated with a significant disconnection between field monitoring data and knowledge about the data. Comprehensive field measurement datasets have not been fully exploited for scientific research and emission regulations. This situation can be considerably improved if the currently available data are better interpreted and the new knowledge is applied to update ammonia emission modeling techniques. The world’s largest agricultural air quality monitoring database with more than 2.4 billion data points has recently been created by the United States’ National Air Emission Monitoring Study. New approaches of data mining and intelligent interpretation of the database are planned to uncover new knowledge and to answer a series of questions that have been raised. The expected results of this new research idea include enhanced fundamental understanding of ammonia emissions from animal agriculture and improved accuracy and scope in regional and national ammonia emission inventories.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2011-05-16</prism:publicationDate>
	<prism:volume>2</prism:volume>
	<prism:number>2</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos2020110</prism:doi>
	<prism:startingPage>110</prism:startingPage>
		<prism:endingPage>128</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Improving Ammonia Emission Modeling and Inventories by Data Mining and Intelligent Interpretation of the National Air Emission Monitoring Study Database]]></dc:title>
    <dc:date>2011-05-16</dc:date>
	<dc:identifier>doi: 10.3390/atmos2020110</dc:identifier>
    	<dc:creator>Ji-Qin Ni</dc:creator>
		<dc:creator>Erin L. Cortus</dc:creator>
		<dc:creator>Albert J. Heber</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/2/2/96">
	<title><![CDATA[Atmosphere, Vol. 2, Pages 96-109: Effects of Floor Level and Building Type on Residential Levels of Outdoor and Indoor Polycyclic Aromatic Hydrocarbons, Black Carbon, and Particulate Matter in New York City]]></title>
	<link>http://www.mdpi.com/2073-4433/2/2/96</link>
	<description>Consideration of the relationship between residential floor level and concentration of traffic-related airborne pollutants may predict individual residential exposure among inner city dwellers more accurately. Our objective was to characterize the vertical gradient of residential levels of polycyclic aromatic hydrocarbons (PAH; dichotomized into Σ8PAHsemivolatile (MW 178–206), and Σ8PAHnonvolatile (MW 228–278), black carbon (BC), PM2.5 (particulate matter) by floor level (FL), season and building type. We hypothesize that PAH, BC and PM2.5 concentrations may decrease with higher FL and the vertical gradients of these compounds would be affected by heating season and building type. PAH, BC and PM2.5 were measured over a two-week period outdoor and indoor of the residences of a cohort of 5–6 year old children (n = 339) living in New York City’s Northern Manhattan and the Bronx. Airborne-pollutant levels were analyzed by three categorized FL groups (0–2nd, 3rd–5th, and 6th–32nd FL) and two building types (low-rise versus high-rise apartment building). Indoor Σ8PAHnonvolatile and BC levels declined with increasing FL. During the nonheating season, the median outdoor Σ8PAHnonvolatile, but not Σ8PAHsemivolatile, level at 6th–2nd FL was 1.5–2 times lower than levels measured at lower FL. Similarly, outdoor and indoor BC concentrations at 6th–32nd FL were significantly lower than those at lower FL only during the nonheating season (p &amp;lt; 0.05). In addition, living in a low-rise building was associated significantly with higher levels of Σ8PAHnonvolatile and BC. These results suggest that young inner city children may be exposed to varying levels of air pollutants depending on their FL, season, and building type.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2011-05-16</prism:publicationDate>
	<prism:volume>2</prism:volume>
	<prism:number>2</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos2020096</prism:doi>
	<prism:startingPage>96</prism:startingPage>
		<prism:endingPage>109</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Effects of Floor Level and Building Type on Residential Levels of Outdoor and Indoor Polycyclic Aromatic Hydrocarbons, Black Carbon, and Particulate Matter in New York City]]></dc:title>
    <dc:date>2011-05-16</dc:date>
	<dc:identifier>doi: 10.3390/atmos2020096</dc:identifier>
    	<dc:creator>Kyung Hwa Jung</dc:creator>
		<dc:creator>Kerlly Bernabé</dc:creator>
		<dc:creator>Kathleen Moors</dc:creator>
		<dc:creator>Beizhan Yan</dc:creator>
		<dc:creator>Steven N. Chillrud</dc:creator>
		<dc:creator>Robin Whyatt</dc:creator>
		<dc:creator>David Camann</dc:creator>
		<dc:creator>Patrick L. Kinney</dc:creator>
		<dc:creator>Frederica P. Perera</dc:creator>
		<dc:creator>Rachel L. Miller</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/2/2/67">
	<title><![CDATA[Atmosphere, Vol. 2, Pages 67-95: The Importance of Lateral Boundaries, Surface Forcing and Choice of Domain Size for Dynamical Downscaling of Global Climate Simulations]]></title>
	<link>http://www.mdpi.com/2073-4433/2/2/67</link>
	<description>Dynamical downscaling by atmospheric Regional Climate Models (RCMs) forced with low-resolution data should produce climate details and add quality and value to the low-resolution data. The aim of this study was to explore the importance of (i) the oceanic surface forcing (sea-surface temperature (SST) and sea-ice), (ii) the lateral boundary condition data, and (iii) the size of the integration domain with respect to improved quality and value in dynamically downscaled data. Experiments addressing the three aspects were performed and the results were investigated for mean sea level pressure (mslp), 2 m air temperature (T2m) and daily precipitation. Although changes in SST gave a clear response locally, changes in the lateral boundary data and the size of the integration domain turned out to be more important with our geographical scope being Norway. The T2m turned out less sensitive to the changes in lateral forcing and the size of the integration domain than mslp and precipitation. The sensitivity for all three variables differed between Norwegian regions; northern parts of Norway were the most sensitive. Even though the sensitivities found in this study might be different in other regions and for other RCMs, these results call for careful consideration when choosing integration domain and driving lateral boundary data when performing dynamical downscaling.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2011-05-11</prism:publicationDate>
	<prism:volume>2</prism:volume>
	<prism:number>2</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos2020067</prism:doi>
	<prism:startingPage>67</prism:startingPage>
		<prism:endingPage>95</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[The Importance of Lateral Boundaries, Surface Forcing and Choice of Domain Size for Dynamical Downscaling of Global Climate Simulations]]></dc:title>
    <dc:date>2011-05-11</dc:date>
	<dc:identifier>doi: 10.3390/atmos2020067</dc:identifier>
    	<dc:creator>Morten A.Ø. Køltzow</dc:creator>
		<dc:creator>Trond Iversen</dc:creator>
		<dc:creator>Jan Erik Haugen</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/2/2/57">
	<title><![CDATA[Atmosphere, Vol. 2, Pages 57-66: Diurnal Cycle of the North American Monsoon in a Mesoscale Model Simulation: Evolution of Key Parameters in Relation to Precipitation]]></title>
	<link>http://www.mdpi.com/2073-4433/2/2/57</link>
	<description>The diurnal cycle of the North American monsoon is analyzed based on the output from a mesoscale model simulation. Statistically significant diurnal cycle in precipitation is identified, with heavy precipitation—essentially convective—dominating in local afternoons. Temporal evolution of key parameters in relation to precipitation is investigated, based on which a sequence of the dynamic/thermodynamic processes underlying precipitation development is proposed. Particularly, the afternoon peak in precipitation is found preceded by enhanced static instability and low-level convergence.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2011-04-06</prism:publicationDate>
	<prism:volume>2</prism:volume>
	<prism:number>2</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos2020057</prism:doi>
	<prism:startingPage>57</prism:startingPage>
		<prism:endingPage>66</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Diurnal Cycle of the North American Monsoon in a Mesoscale Model Simulation: Evolution of Key Parameters in Relation to Precipitation]]></dc:title>
    <dc:date>2011-04-06</dc:date>
	<dc:identifier>doi: 10.3390/atmos2020057</dc:identifier>
    	<dc:creator>Bin Guan</dc:creator>
		<dc:creator>Weizhong Zheng</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/2/2/36">
	<title><![CDATA[Atmosphere, Vol. 2, Pages 36-56: Challenges and Approaches for Developing Ultrafine Particle Emission Inventories for Motor Vehicle and Bus Fleets]]></title>
	<link>http://www.mdpi.com/2073-4433/2/2/36</link>
	<description>Motor vehicles in urban areas are the main source of ultrafine particles (diameters &amp;lt; 0.1 µm). Ultrafine particles are generally measured in terms of particle number because they have little mass and are prolific in terms of their numbers. These sized particles are of particular interest because of their ability to enter deep into the human respiratory system and contribute to negative health effects. Currently ultrafine particles are neither regularly monitored nor regulated by ambient air quality standards. Motor vehicle and bus fleet inventories, epidemiological studies and studies of the chemical composition of ultrafine particles are urgently needed to inform scientific debate and guide development of air quality standards and regulation to control this important pollution source. This article discusses some of the many challenges associated with modelling and quantifying ultrafine particle concentrations and emission rates for developing inventories and microscale modelling of motor vehicles and buses, including the challenge of understanding and quantifying secondary particle formation. Recommendations are made concerning the application of particle emission factors in developing ultrafine particle inventories for motor vehicle fleets. The article presents a précis of the first published inventory of ultrafine particles (particle number) developed for the urban South-East Queensland motor vehicle and bus fleet in Australia, and comments on the applicability of the comprehensive set of average particle emission factors used in this inventory, for developing ultrafine particle (particle number) and particle mass inventories in other developed countries.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2011-03-24</prism:publicationDate>
	<prism:volume>2</prism:volume>
	<prism:number>2</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos2020036</prism:doi>
	<prism:startingPage>36</prism:startingPage>
		<prism:endingPage>56</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Challenges and Approaches for Developing Ultrafine Particle Emission Inventories for Motor Vehicle and Bus Fleets]]></dc:title>
    <dc:date>2011-03-24</dc:date>
	<dc:identifier>doi: 10.3390/atmos2020036</dc:identifier>
    	<dc:creator>Diane U. Keogh</dc:creator>
		<dc:creator>Darrell Sonntag</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/2/2/21">
	<title><![CDATA[Atmosphere, Vol. 2, Pages 21-35: An Analytical Simple Formula for the Ground Level Concentration from a Point Source]]></title>
	<link>http://www.mdpi.com/2073-4433/2/2/21</link>
	<description>The Advection-Diffusion Equation is solved for a constant pollutant emission from a point-like source placed inside an unstable Atmospheric Boundary Layer. The solution is obtained adopting the novel analytical approach: Generalized Integral Laplace Transform Technique. The concentration solution of the equation is expressed through an infinite series expansion. After setting a realistic scenario through the wind and diffusivity parameterizations, the Ground Level Concentration (GLC) is determined, and an explicit approximate expression is provided for it, allowing an analytically simple expression for the position and value of the maximum. Remarks arise regarding the ability to express value and position of the GLC as explicit functions of the parameters defining the Atmospheric Boundary Layer scenario and the source height.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2011-03-24</prism:publicationDate>
	<prism:volume>2</prism:volume>
	<prism:number>2</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos2020021</prism:doi>
	<prism:startingPage>21</prism:startingPage>
		<prism:endingPage>35</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[An Analytical Simple Formula for the Ground Level Concentration from a Point Source]]></dc:title>
    <dc:date>2011-03-24</dc:date>
	<dc:identifier>doi: 10.3390/atmos2020021</dc:identifier>
    	<dc:creator>Tiziano Tirabassi</dc:creator>
		<dc:creator>Alessandro Tiesi</dc:creator>
		<dc:creator>Marco T. Vilhena</dc:creator>
		<dc:creator>Bardo E.J. Bodmann</dc:creator>
		<dc:creator>Daniela Buske</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/2/1/1">
	<title><![CDATA[Atmosphere, Vol. 2, Pages 1-20: Comparison of Particulate Mercury Measured with Manual and Automated Methods]]></title>
	<link>http://www.mdpi.com/2073-4433/2/1/1</link>
	<description>A study was conducted to compare measuring particulate mercury (HgP) with the manual filter method and the automated Tekran system. Simultaneous measurements were conducted with the Tekran and Teflon filter methodologies in the marine and coastal continental atmospheres. Overall, the filter HgP values were on the average 21% higher than the Tekran HgP, and &amp;gt;85% of the data were outside of ±25% region surrounding the 1:1 line. In some cases the filter values were as much as 3-fold greater, with</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2011-01-20</prism:publicationDate>
	<prism:volume>2</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos2010001</prism:doi>
	<prism:startingPage>1</prism:startingPage>
		<prism:endingPage>20</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Comparison of Particulate Mercury Measured with Manual and Automated Methods]]></dc:title>
    <dc:date>2011-01-20</dc:date>
	<dc:identifier>doi: 10.3390/atmos2010001</dc:identifier>
    	<dc:creator>Robert Talbot</dc:creator>
		<dc:creator>Huiting Mao</dc:creator>
		<dc:creator>Dara Feddersen</dc:creator>
		<dc:creator>Melissa Smith</dc:creator>
		<dc:creator>Su Youn Kim</dc:creator>
		<dc:creator>Barkley Sive</dc:creator>
		<dc:creator>Karl Haase</dc:creator>
		<dc:creator>Jesse Ambrose</dc:creator>
		<dc:creator>Yong Zhou</dc:creator>
		<dc:creator>Rachel Russo</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/1/1/62">
	<title><![CDATA[Atmosphere, Vol. 1, Pages 62-84: The Influence of Stratospheric Sulphate Aerosol Deployment on the Surface Air Temperature and the Risk of an Abrupt Global Warming]]></title>
	<link>http://www.mdpi.com/2073-4433/1/1/62</link>
	<description>We used the ‘Radiative-Convective Model of the Earth-atmosphere system’ (OGIM) to investigate the cooling effects induced by sulphur injections into the stratosphere. The ensemble of numerical calculations was based on the A1B scenario from the IPCC Special Report on Emissions Scenarios (SRES). Several geoengineered scenarios were analysed, including the abrupt interruption of these injections in different scenarios and at different dates. We focused on the surface air temperature (SAT) anomalies induced by stratospheric sulphate aerosol generated in order to compensate future warming. Results show that continuous deployment of sulphur into the stratosphere could induce a lasting decrease in SAT. Retaining a constant aerosol loading equivalent to 6 TgS would delay the expected global warming by 53 years. Keeping the SAT constant in a context of increasing greenhouse gases (GHGs) means that the aerosol loading needs to be increased by 1.9% annually. This would offset the effect of increasing GHG under the A1B scenario. A major focus of this study was on the heating rates of SAT that would arise in different scenarios in case of an abrupt cessation of sulphur injections into the stratosphere. Our model results show that heating rates after geoengineering interruption would be 15–28 times higher than in a case without geoengineering, with likely important consequences for life on Earth. Larger initial sulphate loadings induced more intense warming rates when the geoengineering was stopped at the same time. This implies that, if sulphate loading was increased to maintain constant SAT in the light of increasing GHG concentrations, the later the geoengineering interruption was to occur, the higher the heating rates would be. Consequently, geoengineering techniques like this should only be regarded as last-resort measures and require intense further research should they ever become necessary.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2010-12-10</prism:publicationDate>
	<prism:volume>1</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos1010062</prism:doi>
	<prism:startingPage>62</prism:startingPage>
		<prism:endingPage>84</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[The Influence of Stratospheric Sulphate Aerosol Deployment on the Surface Air Temperature and the Risk of an Abrupt Global Warming]]></dc:title>
    <dc:date>2010-12-10</dc:date>
	<dc:identifier>doi: 10.3390/atmos1010062</dc:identifier>
    	<dc:creator>Pedro Llanillo</dc:creator>
		<dc:creator>Phil D. Jones</dc:creator>
		<dc:creator>Roland Von Glasow</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/1/1/51">
	<title><![CDATA[Atmosphere, Vol. 1, Pages 51-61: Assessment of Maximum Possible Urbanization Influences on Land Temperature Data by Comparison of Land and Marine Data around Coasts]]></title>
	<link>http://www.mdpi.com/2073-4433/1/1/51</link>
	<description>Global surface temperature trends, based on land and marine data, show warming of about 0.8 °C over the last 100 years. This rate of warming is sometimes questioned because of the existence of Urban Heat Islands (UHIs). In this study we compare the rate of temperature change estimated from measurements of land and marine temperatures for the same grid squares using 5° by 5° latitude/longitude grid-box datasets. For 1951–2009 the ‘land’ average warmed by 0.02 °C decade−1 relative to the ‘sea surface temperature’ (SST) average. There were regional contrasts in the trends of land/sea temperature differences: the land warmed at a greater rate compared to the SST for regions north of 20°S, but the opposite occurred further south. Given strong forcing of the climate system, we would expect the land to change more rapidly than the ocean, so the differences represent an upper limit to the urbanization effect.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2010-12-06</prism:publicationDate>
	<prism:volume>1</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos1010051</prism:doi>
	<prism:startingPage>51</prism:startingPage>
		<prism:endingPage>61</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Assessment of Maximum Possible Urbanization Influences on Land Temperature Data by Comparison of Land and Marine Data around Coasts]]></dc:title>
    <dc:date>2010-12-06</dc:date>
	<dc:identifier>doi: 10.3390/atmos1010051</dc:identifier>
    	<dc:creator>Dimitrios A. Efthymiadis</dc:creator>
		<dc:creator>Philip D. Jones</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/1/1/34">
	<title><![CDATA[Atmosphere, Vol. 1, Pages 34-50: Oceanic Dimethyl Sulfide Emission and New Particle Formation around the Coast of Antarctica: A Modeling Study of Seasonal Variations and Comparison with Measurements]]></title>
	<link>http://www.mdpi.com/2073-4433/1/1/34</link>
	<description>A clear understanding of new particle formation processes in remote oceans is critical for properly assessing the role of oceanic dimethyl sulfide (DMS) emission on the Earth’s climate and associated climate feedback processes. Almost free from anthropogenic pollutants and leafed plants, the Antarctic continent and surrounding oceans are unique regions for studying the lifecycle of natural sulfate aerosols. Here we investigate the well-recognized seasonal variations of new particle formation around Antarctic coastal areas with a recently developed global size-resolved aerosol model. Our simulations indicate that enhanced DMS emission and photochemistry during the austral summer season lead to significant new particle formation via ion-mediated nucleation (IMN) and much higher particle number concentrations over Antarctica and surrounding oceans. By comparing predicted condensation nuclei larger than 10 nm (CN10) during a three-year period (2005–2007) with the long-period continuous CN10 measurements at the German Antarctic station Neumayer, we show that the model captures the absolute values of monthly mean CN10 (within a factor 2–3) as well as their seasonal variations. Our simulations confirm that the observed Antarctic CN10 and cloud condensation nuclei (CCN) seasonal variations are due to the formation of secondary particles during the austral summer. From the austral winter to summer, the zonally averaged CN10 and CCN in the lower troposphere over Antarctica increase by a factor of ~4–6 and ~2–4, respectively. This study appears to show that the H2SO4-H2O IMN mechanism is able to account for the new particle formation frequently observed in the Antarctica region during the austral summer.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2010-12-06</prism:publicationDate>
	<prism:volume>1</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos1010034</prism:doi>
	<prism:startingPage>34</prism:startingPage>
		<prism:endingPage>50</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Oceanic Dimethyl Sulfide Emission and New Particle Formation around the Coast of Antarctica: A Modeling Study of Seasonal Variations and Comparison with Measurements]]></dc:title>
    <dc:date>2010-12-06</dc:date>
	<dc:identifier>doi: 10.3390/atmos1010034</dc:identifier>
    	<dc:creator>Fangqun Yu</dc:creator>
		<dc:creator>Gan Luo</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/1/1/15">
	<title><![CDATA[Atmosphere, Vol. 1, Pages 15-33: Remote Sensing and Modeling of Cyclone Monica near Peak Intensity]]></title>
	<link>http://www.mdpi.com/2073-4433/1/1/15</link>
	<description>Cyclone Monica was an intense Southern Hemisphere tropical cyclone of 2006. Although no in situ measurements of Monica’s inner core were made, microwave, infrared, and visible satellite instruments observed Monica before and during peak intensity through landfall on Australia’s northern coast. The author analyzes remote sensing measurements in detail to investigate Monica’s intensity. While Dvorak analysis of its imagery argues that it was of extreme intensity, infrared and microwave soundings indicate a somewhat lower intensity, especially as it neared landfall. The author also describes several numerical model runs that were made to investigate the maximum possible intensity for the observed environmental conditions; these simulations also suggest a lower intensity than estimates from Dvorak analysis alone. Based on the evidence from the various measurements and modeling, the estimated range for the minimum sea level pressure at peak intensity is 900 to 920 hPa. The estimated range for the one-minute averaged maximum wind speed at peak intensity is 72 to 82 m/s. These maxima were likely reached about 24 hours prior to landfall, with some weakening occurring afterward.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2010-07-12</prism:publicationDate>
	<prism:volume>1</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos1010015</prism:doi>
	<prism:startingPage>15</prism:startingPage>
		<prism:endingPage>33</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Remote Sensing and Modeling of Cyclone Monica near Peak Intensity]]></dc:title>
    <dc:date>2010-07-12</dc:date>
	<dc:identifier>doi: 10.3390/atmos1010015</dc:identifier>
    	<dc:creator>Stephen L. Durden</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/1/1/3">
	<title><![CDATA[Atmosphere, Vol. 1, Pages 3-14: Correlation of Air Quality Data to Ultrafine Particles (UFP) Concentration and Size Distribution in Ambient Air]]></title>
	<link>http://www.mdpi.com/2073-4433/1/1/3</link>
	<description>This study monitored ultrafine particles (UFP) concurrent with environmental air quality data, investigating whether already existing instrumentation used by environmental authorities can provide reference values for estimating UFP concentrations. Of particular interest was the relation of UFP to PM10 (particulate matter) and nitrogen oxides (NOx, NO2) in ambient air. Existing PM measurement methods alone did not correspond exactly enough with the actual particle number, but we observed a link between NOx and NO2 to UFP concentration. The combined data could act as proxy-indicator for authorities in estimating particle number concentrations, but cannot replace UFP monitoring.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2010-07-12</prism:publicationDate>
	<prism:volume>1</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Article</prism:section>
	<prism:doi>10.3390/atmos1010003</prism:doi>
	<prism:startingPage>3</prism:startingPage>
		<prism:endingPage>14</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Correlation of Air Quality Data to Ultrafine Particles (UFP) Concentration and Size Distribution in Ambient Air]]></dc:title>
    <dc:date>2010-07-12</dc:date>
	<dc:identifier>doi: 10.3390/atmos1010003</dc:identifier>
    	<dc:creator> Kwasny</dc:creator>
		<dc:creator> Madl</dc:creator>
		<dc:creator> Hofmann</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
        <item rdf:about="http://www.mdpi.com/2073-4433/1/1/1">
	<title><![CDATA[Atmosphere, Vol. 1, Pages 1-2: Atmosphere: An International and Interdisciplinary Scientific Open Access Journal]]></title>
	<link>http://www.mdpi.com/2073-4433/1/1/1</link>
	<description>The new online, Open Access journal Atmosphere has been launched to present reviews, regular research papers, communications and short notes on atmospheric topics. These topics include experimental and theoretical work related to the physical atmosphere, such as turbulence, atmospheric flow, dynamic and physical processes and mechanisms, atmospheric chemistry, such as changes in atmospheric composition, including aerosols, ozone, air pollution, chemical weather, meteorology and scale interaction, climate, climate change and environmental science, including water and energy cycles.</description>

	<prism:publicationName>Atmosphere</prism:publicationName>
	<prism:publicationDate>2010-07-09</prism:publicationDate>
	<prism:volume>1</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Editorial</prism:section>
	<prism:doi>10.3390/atmos1010001</prism:doi>
	<prism:startingPage>1</prism:startingPage>
		<prism:endingPage>2</prism:endingPage>
		<prism:issn>2073-4433</prism:issn>
	
	<dc:title><![CDATA[Atmosphere: An International and Interdisciplinary Scientific Open Access Journal]]></dc:title>
    <dc:date>2010-07-09</dc:date>
	<dc:identifier>doi: 10.3390/atmos1010001</dc:identifier>
    	<dc:creator> Jacob</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
    
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