A short climatology of nanoparticles at the Cape Grim Baseline Air Pollution Station, Tasmania

2007 ◽  
Vol 4 (5) ◽  
pp. 301 ◽  
Author(s):  
S. I. Jimi ◽  
J.L. Gras ◽  
S. T. Siems ◽  
P. B. Krummel

Environmental context. Atmospheric particles play an important role in the global climate system; they contribute to the radiation balance directly, but they also have an indirect effect by modifying cloud properties and influencing precipitation. Over the Southern Ocean, nanometre-sized particle production is believed to be largely natural, although the processes that lead to these particles are not well understood. This work provides new observations of atmospheric nanoparticles, and shows that they arise from diverse sources of production. Abstract. This paper presents analyses of a two-year record of aerosol measurements made at the Cape Grim Baseline Air Pollution Station (CGBAPS) in Tasmania covering the period 1999 and 2000. The focus of the study is nanoparticles, defined here as particles with diameter Dp, in the range 3 ≤ Dp ≤ 12 nm; with the number concentration determined using two condensation particle counters, a TSI 3025 UCPC (Dp ≥ 3 nm) and a TSI CN3760 (Dp ≥ 12 nm). Total aerosol (Dp ≥ 3 nm) and nanoparticle concentrations were examined for three broad air mass origins, namely ‘Baseline’ or background maritime, continental Australia and Tasmanian air masses. Total median aerosol concentrations in the Baseline, continental and Tasmanian sectors typically ranged from 100 to 900, 1300 to 1900 and 500 to 1200 cm–3, respectively. The median ranges for the nanoparticle concentrations were 50–350 cm–3 in Baseline air, 150–450 cm–3 in continental air and 100–300 cm–3 in Tasmanian air. While the total aerosol concentrations in the three sectors were quite different, the nanoparticle concentrations were less so. Nanoparticle diurnal concentrations showed substantial differences between the three sectors, indicative of different aerosol sources or precursor sources in the regions designated by these wind sectors.


2008 ◽  
Vol 8 (20) ◽  
pp. 6155-6168 ◽  
Author(s):  
B. Wehner ◽  
W. Birmili ◽  
F. Ditas ◽  
Z. Wu ◽  
M. Hu ◽  
...  

Abstract. The Chinese capital Beijing is one of the global megacities where the effects of rapid economic growth have led to complex air pollution problems that are not well understood. In this study, ambient particle number size distributions in Beijing between 2004 and 2006 are analysed as a function of regional meteorological transport. An essential result is that the particle size distribution in Beijing depends to large extent on the history of the synoptic scale air masses. A first approach based on manual back trajectory classification yielded differences in particulate matter mass concentration by a factor of two between four different air mass categories, including three main wind directions plus the case of stagnant air masses. A back trajectory cluster analysis refined these results, yielding a total of six trajectory clusters. Besides the large scale wind direction, the transportation speed of an air mass was found to play an essential role on the PM concentrations in Beijing. Slow-moving air masses were shown to be associated with an effective accumulation of surface-based anthropogenic emissions due to both, an increased residence time over densely populated land, and their higher degree of vertical stability. For the six back trajectory clusters, differences in PM1 mass concentrations by a factor of 3.5, in the mean air mass speed by a factor of 6, and in atmospheric visibility by a factor of 4 were found. The main conclusion is that the air quality in Beijing is not only degraded by anthropogenic aerosol sources from within the megacity, but also by sources across the entire Northwest China plain depending on the meteorological situation.



2009 ◽  
Vol 6 (6) ◽  
pp. 508 ◽  
Author(s):  
John L. Gras ◽  
Salah I. Jimi ◽  
Steven T. Siems ◽  
Paul B. Krummel

Environmental context. Clouds and the factors controlling cloud properties are essential components in understanding and accurately predicting global climate change. This work examines nanometre-sized atmospheric particles, particularly bursts of enhanced particle concentrations following cold fronts over the Southern Ocean. The properties of these events have been established to enable modelling of their significance as a source of cloud-droplet-forming nuclei. Abstract. Nanoparticles (diameter <10 nm) were studied in clean maritime air at Cape Grim over a 2-year period. Concentrations were determined using a condensation nucleus counter (CNC) and an ultra-CNC (UCNC), requiring careful treatment of drifts in counter efficiency. This is the first extended examination of nanoparticles following cold fronts and shows that nanoparticle enhancements were present following 94% of 121 cold fronts studied. Typical enhancements were ~100 cm–3 with maxima ~300–500 cm–3, occur 9–11 h after the front and contain multiple peaks with peak-to-peak separation of 8–11 h. Most enhancements were associated with drier conditions, indicative of increased entrainment of free-tropospheric air after the front. The quasi-periodicity of the enhancements may be related to mesoscale structures in cloud fields following fronts but this requires testing. This quantification of event properties allows evaluation of the significance of these events for the cloud nucleating particle (CCN) population.



2009 ◽  
Vol 9 (4) ◽  
pp. 1465-1478 ◽  
Author(s):  
H. Venzac ◽  
K. Sellegri ◽  
P. Villani ◽  
D. Picard ◽  
P. Laj

Abstract. Particle number concentration and size distribution are important variables needed to constrain the role of atmospheric particles in the Earth radiation budget, both directly and indirectly through CCN activation. They are also linked to regulated variables such as particle mass (PM) and therefore of interest to air quality studies. However, data on their long-term variability are scarce, in particular at high altitudes. In this paper, we investigate the diurnal and seasonal variability of the aerosol total number concentration and size distribution at the puy de Dôme research station (France, 1465 m a.s.l.). We report a variability of aerosol particle total number concentration measured over a five-year (2003–2007) period for particles larger than 10 nm and aerosol size distributions between 10 and 500 nm over a two-year period (January 2006 to December 2007). Concentrations show a strong seasonality with maxima during summer and minima during winter. A diurnal variation is also observed with maxima between 12:00 and 18:00 UTC. At night (00:00–06:00 UTC), the median hourly total concentration varies from 600 to 800 cm−3 during winter and from 1700 to 2200 cm−3 during summer. During the day (08:00–18:00 UTC), the concentration is in the range of 700 to 1400 cm−3 during winter and of 2500 to 3500 cm−3 during summer. An averaged size distribution of particles (10–500 nm) was calculated for each season. The total aerosol number concentrations are dominated by the Aitken mode integral concentrations, which drive most of the winter to summer total concentrations increase. The night to day increase in dominated by the nucleation mode integral number concentration. Because the site is located in the free troposphere only a fraction of the time, in particular at night and during the winter season, we have subsequently analyzed the variability for nighttime and free tropospheric (FT)/residual layer (RL) conditions only. We show that a seasonal variability is still observed for these FT/RL conditions. The FT/RL seasonal variation is due to both seasonal changes in the air mass origin from winter to summer and enhanced concentrations of particles in the residual layer/free troposphere in summer. The later observation can be explained by higher emissions intensity in the boundary layer, stronger exchanges between the boundary layer and the free troposphere as well as enhanced photochemical processes. Finally, aerosols mean size distributions are calculated for a given air mass type (marine/continental/regional) according to the season for the specific conditions of the residual layer/free troposphere. The seasonal variability in aerosol sources seems to be predominant over the continent compared to the seasonal variation of marine aerosol sources. These results are of regional relevance and can be used to constrain chemical-transport models over Western Europe.



2008 ◽  
Vol 8 (3) ◽  
pp. 11321-11362 ◽  
Author(s):  
B. Wehner ◽  
W. Birmili ◽  
F. Ditas ◽  
Z. Wu ◽  
M. Hu ◽  
...  

Abstract. The Chinese capital Beijing is one of the global megacities where the effects of rapid economic growth have led to complex air pollution problems that are not well understood. In this study, ambient particle number size distributions in Beijing between 2004 and 2006 are analysed as a function of regional meteorological transport. An essential result is that the particle size distribution in Beijing depends to large extent on the history of the synoptic scale air masses. A first approach based on manual back trajectory classification yielded differences in particulate matter mass concentration (PM1 and PM10) by a factor of two between four different air mass categories, including three main wind directions plus the case of stagnant air masses. A back trajectory cluster analysis refined these results, yielding a total of six trajectory clusters. Besides the large scale wind direction, the transportation speed of an air mass was found to play an essential role on the PM concentrations in Beijing. Slow-moving air masses were shown to be associated with an effective accumulation of surface-based anthropogenic emissions due to both, an increased residence time over densely populated land, and their higher degree of vertical stability. For the six back trajectory clusters, differences in PM1 mass concentrations by a factor of 3.5, in the mean air mass speed by a factor of 6, and in atmospheric visibility by a factor of 4 were found. The main conclusion is that the air quality in Beijing is not only degraded by anthropogenic aerosol sources from within the megacity, but also by sources across the entire Northwest China plain depending on the meteorological situation.



2016 ◽  
Author(s):  
Justin H. Dingle ◽  
Kennedy Vu ◽  
Roya Bahreini ◽  
Eric C. Apel ◽  
Teresa L. Campos ◽  
...  

Abstract. Summertime aerosol optical extinction (βext) was measured in the Colorado Front Range and Denver Metropolitan Area as part of the Front Range Air Pollution and Photochemistry Experiment (FRAPPÉ) campaign during July–August 2014. An Aerodyne Cavity Attenuated Phase Shift particle light extinction monitor (CAPS-PMex) was deployed to measure dry, βext of submicron aerosols at λ = 632 nm at 1 Hz. Data from a suite of gas-phase instrumentation were used to interpret βext behavior under various categories of air masses and sources. Extinction enhancement ratios relative to CO (Δβext/ΔCO) were significantly increased in highly aged air masses compared to fresh air masses by 50–60 %. The resulting increase in Δβext/ΔCO under highly aged air masses was accompanied by formation of secondary organic aerosols (SOA). In addition, the impacts of aerosol composition on βext in air masses under the influence of urban, natural oil and gas operations (O&amp;G), and agriculture and livestock operations were evaluated. Estimated non-refractory mass extinction efficiency (MEE) values for different air mass types ranged from 1.83–3.30 m2 g−1, with the minimum and maximum values observed in agriculture and urban + O&amp;G influenced air masses, respectively. The mass distribution for organic, nitrate, and sulfate aerosols presented distinct profiles in different air mass types. During Aug. 11–12, regional influence of a biomass burning event was observed, increasing the background βext by 10–15 Mm−1 and the estimated MEE and Δβext/ΔCO values in the Front Range.



2019 ◽  
Author(s):  
Joel Alroe ◽  
Luke T. Cravigan ◽  
Branka Miljevic ◽  
Graham R. Johnson ◽  
Paul Selleck ◽  
...  

Abstract. Cloud-radiation interactions over the Southern Ocean are not well constrained in climate models, in part due to uncertainties in the sources, concentrations and cloud-forming potential of aerosol in this region. To date, most studies in this region have reported measurements from fixed terrestrial stations or a limited set of instrumentation, and often present findings as broad seasonal or latitudinal trends. Here, we present an extensive set of aerosol and meteorological observations obtained during an austral summer cruise across the full width of the Southern Ocean south of Australia. Three episodes of continental-influenced air masses were identified, including an apparent transition between the Ferrel atmospheric cell and the polar cell at approximately 64° S. During the other two episodes, synoptic-scale weather patterns diverted air masses across distances greater than 1000 km from the Australian and Antarctic coastlines, respectively, indicating that a large proportion of the Southern Ocean may be periodically influenced by continental air masses. In all three cases, a highly cloud-active accumulation mode dominated the size distribution, with up to 93 % of the total number concentration activating as cloud condensation nuclei. In contrast, sampling periods influenced by marine air masses frequently demonstrated a correlation between air mass trajectories over regions of high biological productivity and subsequent enhancement of an Aitken mode centred at approximately 30 nm and contributing an average of 71 % of the total aerosol number concentration. Although these small diameters limited their contribution to cloud condensation nuclei concentrations, Aitken number concentrations and diameters were highly variable. A detailed investigation of the marine air masses revealed that this variability may be attributed to the availability of biogenic precursors, the competing influence of condensation sinks (such as sea spray aerosol) and vertical transport between the marine boundary layer and the free troposphere. This variability of the marine Aitken mode as well as the instances of long-range transport were governed by synoptic-scale weather systems, through their influence on air mass trajectories and both generation and depletion of condensation sinks. These results demonstrate the highly dynamic nature of Southern Ocean aerosol and their complex dependence on both biological productivity and synoptic-scale weather systems.



2016 ◽  
Vol 16 (17) ◽  
pp. 11207-11217 ◽  
Author(s):  
Justin H. Dingle ◽  
Kennedy Vu ◽  
Roya Bahreini ◽  
Eric C. Apel ◽  
Teresa L. Campos ◽  
...  

Abstract. Summertime aerosol optical extinction (βext) was measured in the Colorado Front Range and Denver metropolitan area as part of the Front Range Air Pollution and Photochemistry Éxperiment (FRAPPÉ) campaign during July–August 2014. An Aerodyne cavity attenuated phase shift particle light extinction monitor (CAPS-PMex) was deployed to measure βext (at average relative humidity of 20 ± 7 %) of submicron aerosols at λ = 632 nm at 1 Hz. Data from a suite of gas-phase instrumentation were used to interpret βext behavior in various categories of air masses and sources. Extinction enhancement ratios relative to CO (Δβext ∕ ΔCO) were higher in aged urban air masses compared to fresh air masses by  ∼  50 %. The resulting increase in Δβext ∕ ΔCO for highly aged air masses was accompanied by formation of secondary organic aerosols (SOAs). In addition, the impacts of aerosol composition on βext in air masses under the influence of urban, natural oil and gas operations (O&amp;G), and agriculture and livestock operations were evaluated. Estimated non-refractory mass extinction efficiency (MEE) values for different air mass types ranged from 1.51 to 2.27 m2 g−1, with the minimum and maximum values observed in urban and agriculture-influenced air masses, respectively. The mass distribution for organic, nitrate, and sulfate aerosols presented distinct profiles in different air mass types. During 11–12 August, regional influence of a biomass burning event was observed, increasing the background βext and estimated MEE values in the Front Range.



2006 ◽  
Vol 6 (1) ◽  
pp. 879-898 ◽  
Author(s):  
R. Dupuy ◽  
P. Laj ◽  
K. Sellegri

Abstract. The fraction of aerosol particles activated to droplets (CCN) is often derived from semi-empirical relationships that commonly tend to overestimate droplet number concentration leading to major uncertainties in global climate models. One of the difficulties in relating aerosol concentration to cloud microphysics and cloud albedo lies in the necessity of working at a constant liquid water path (LWP), which is very difficult to control. In this study we observed the relationships between aerosol number concentration (NCN), cloud droplet concentration (Nd) and effective radius (Reff), at the Puy de Dôme (France). A total of 20 cloud events were sampled representing a period of more than 250 h of cloud sampling. Samples are classified first according to air mass origins (Modified Marine, Continental and Polluted) and then according to their liquid water content (Thin, Medium and Thick clouds). The CCN fraction of aerosols appears to vary significantly according to the air mass origin. It is maximum for Continental air masses and minimum for Polluted air masses. Surprisingly, the CCN fraction of Modified Marine air masses fraction is lower than the continental air mass and from expected from previous studies. The limited number of activated particles in Modified Marine air masses is most likely the result of the presence of hydrophobic organic compounds. The limited activation effect leads to a 0.5 to 1 μm increase in Reff with respect to an ideal Marine case. This is significant and implies that the dReff/dNCN of low-continental clouds is higher than expected.



2010 ◽  
Vol 10 (14) ◽  
pp. 6527-6536 ◽  
Author(s):  
M. A. Brunke ◽  
S. P. de Szoeke ◽  
P. Zuidema ◽  
X. Zeng

Abstract. Here, liquid water path (LWP), cloud fraction, cloud top height, and cloud base height retrieved by a suite of A-train satellite instruments (the CPR aboard CloudSat, CALIOP aboard CALIPSO, and MODIS aboard Aqua) are compared to ship observations from research cruises made in 2001 and 2003–2007 into the stratus/stratocumulus deck over the southeast Pacific Ocean. It is found that CloudSat radar-only LWP is generally too high over this region and the CloudSat/CALIPSO cloud bases are too low. This results in a relationship (LWP~h9) between CloudSat LWP and CALIPSO cloud thickness (h) that is very different from the adiabatic relationship (LWP~h2) from in situ observations. Such biases can be reduced if LWPs suspected to be contaminated by precipitation are eliminated, as determined by the maximum radar reflectivity Zmax>−15 dBZ in the apparent lower half of the cloud, and if cloud bases are determined based upon the adiabatically-determined cloud thickness (h~LWP1/2). Furthermore, comparing results from a global model (CAM3.1) to ship observations reveals that, while the simulated LWP is quite reasonable, the model cloud is too thick and too low, allowing the model to have LWPs that are almost independent of h. This model can also obtain a reasonable diurnal cycle in LWP and cloud fraction at a location roughly in the centre of this region (20° S, 85° W) but has an opposite diurnal cycle to those observed aboard ship at a location closer to the coast (20° S, 75° W). The diurnal cycle at the latter location is slightly improved in the newest version of the model (CAM4). However, the simulated clouds remain too thick and too low, as cloud bases are usually at or near the surface.



2019 ◽  
Vol 19 (19) ◽  
pp. 12477-12494 ◽  
Author(s):  
Armin Sigmund ◽  
Korbinian Freier ◽  
Till Rehm ◽  
Ludwig Ries ◽  
Christian Schunk ◽  
...  

Abstract. To assist atmospheric monitoring at high-alpine sites, a statistical approach for distinguishing between the dominant air masses was developed. This approach was based on a principal component analysis using five gas-phase and two meteorological variables. The analysis focused on the Schneefernerhaus site at Zugspitze Mountain, Germany. The investigated year was divided into 2-month periods, for which the analysis was repeated. Using the 33.3 % and 66.6 % percentiles of the first two principal components, nine air mass regimes were defined. These regimes were interpreted with respect to vertical transport and assigned to the BL (recent contact with the boundary layer), UFT/SIN (undisturbed free troposphere or stratospheric intrusion), and HYBRID (influences of both the boundary layer and the free troposphere or ambiguous) air mass classes. The input data were available for 78 % of the investigated year. BL accounted for 31 % of the cases with similar frequencies in all seasons. UFT/SIN comprised 14 % of the cases but was not found from April to July. HYBRID (55 %) mostly exhibited intermediate characteristics, whereby 17 % of the HYBRID class suggested an influence from the marine boundary layer or the lower free troposphere. The statistical approach was compared to a mechanistic approach using the ceilometer-based mixing layer height from a nearby valley site and a detection scheme for thermally induced mountain winds. Due to data gaps, only 25 % of the cases could be classified using the mechanistic approach. Both approaches agreed well, except in the rare cases of thermally induced uplift. The statistical approach is a promising step towards a real-time classification of air masses. Future work is necessary to assess the uncertainty arising from the standardization of real-time data.



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