Investigation of correlations between the high surface ozone episodes and the stratospheric intrusion events

2005 ◽  
Author(s):  
Vera Grigorieva ◽  
Staytcho Kolev ◽  
Mihail Mihalev
2012 ◽  
Vol 2012 ◽  
pp. 1-7 ◽  
Author(s):  
Nandita D. Ganguly

The surface ozone levels in some Indian cities have increased significantly in the recent years. Ozone being toxic to the living system and an important contributor to anthropogenic global warming, enhanced surface ozone may have adverse effects on the air quality and climate. Transport of ozone from the stratosphere to the troposphere causes stratospheric ozone to decrease and tropospheric ozone to increase, which can in turn have serious consequences for life on earth. Since stratosphere-troposphere exchange (STE) is an important factor influencing the ozone concentration in the troposphere, this paper investigates probably for the first time the possible contribution of STE events to the observed enhanced surface ozone levels for cities covering from north to south of India. It is concluded that apart from transport processes and in situ photochemical production, STE also influences the observed high-surface ozone levels in Indian cities to a small extent (8%–16%). STE events producing high-surface ozone levels are found to be higher at high latitudes.


2012 ◽  
Vol 117 (D21) ◽  
pp. n/a-n/a ◽  
Author(s):  
Meiyun Lin ◽  
Arlene M. Fiore ◽  
Owen R. Cooper ◽  
Larry W. Horowitz ◽  
Andrew O. Langford ◽  
...  

2011 ◽  
Vol 11 (6) ◽  
pp. 2569-2583 ◽  
Author(s):  
H. He ◽  
D. W. Tarasick ◽  
W. K. Hocking ◽  
T. K. Carey-Smith ◽  
Y. Rochon ◽  
...  

Abstract. Twice-daily ozonesondes were launched from Harrow, in southwestern Ontario, Canada, during the BAQS-Met (Border Air Quality and Meteorology Study) field campaign in June and July of 2007. A co-located radar windprofiler measured tropopause height continuously. These data, in combination with continuous surface ozone measurements and geo-statistical interpolation of satellite ozone observations, present a consistent picture and indicate that a number of significant ozone enhancements in the troposphere were observed that were the result of stratospheric intrusion events. The combined observations have also been compared with results from two Environment Canada numerical models, the operational weather prediction model GEM (as input to FLEXPART), and a new version of the regional air quality model AURAMS, in order to examine the ability of these models to accurately represent sporadic cross-tropopause ozone transport events. The models appear to reproduce intrusion events with some skill, implying that GEM dynamics (which also drive AURAMS) are able to represent such events well. There are important differences in the quantitative comparison, however; in particular, the poor vertical resolution of AURAMS around the tropopause causes it to bring down too much ozone in individual intrusions. These campaign results imply that stratospheric intrusions are important to the ozone budget of the mid-latitude troposphere, and appear to be responsible for much of the variability of ozone in the free troposphere. GEM-FLEXPART calculations indicate that stratospheric ozone intrusions contributed significantly to surface ozone on several occasions during the BAQS-Met campaign, and made a moderate but significant contribution to the overall tropospheric ozone budget.


2018 ◽  
Author(s):  
Jean J. Guo ◽  
Arlene M. Fiore ◽  
Lee T. Murray ◽  
Daniel A. Jaffe ◽  
Jordan L. Schnell ◽  
...  

Abstract. U.S. background ozone (O3) includes O3 produced from anthropogenic O3 precursors emitted outside of the U.S.A., from global methane, and from any natural sources. Using a suite of sensitivity simulations in the GEOS-Chem global chemistry-transport model, we estimate the influence from individual background versus U.S. anthropogenic sources on total surface O3 over ten continental U.S. regions from 2004–2012. Evaluation with observations reveals model biases of +0–19 ppb in seasonal mean maximum daily 8-hour average (MDA8) O3, highest in summer over the eastern U.S.A. Simulated high-O3 events cluster too late in the season. We link these model biases to regional O3 production (e.g., U.S. anthropogenic, biogenic volatile organic compounds (BVOC), and soil NOx, emissions), or coincident missing sinks. On the ten highest observed O3 days during summer (O3_top10obs_JJA), U.S. anthropogenic emissions enhance O3 by 5–11 ppb and by less than 2 ppb in the eastern versus western U.S.A. The O3 enhancement from BVOC emissions during summer is 1–7 ppb higher on O3_top10obs_JJA days than on average days, while intercontinental pollution is up to 2 ppb higher on average vs. on O3_top10obs_JJA days. In the model, regional sources of O3 precursor emissions drive interannual variability in the highest observed O3 levels. During the summers of 2004–2012, monthly regional mean U.S. background O3 MDA8 levels vary by 10–20 ppb. Simulated summertime total surface O3 levels on O3_top10obs_JJA days decline by 3 ppb (averaged over all regions) from 2004–2006 to 2010–2012 in both the observations and the model, reflecting rising U.S. background (+2 ppb) and declining U.S. anthropogenic O3 emissions (−6 ppb). The model attributes interannual variability in U.S. background O3 on O3_top10obs days to natural sources, not international pollution transport. We find that a three-year averaging period is not long enough to eliminate interannual variability in background O3.


Elem Sci Anth ◽  
2021 ◽  
Vol 9 (1) ◽  
Author(s):  
Kai-Lan Chang ◽  
Martin G. Schultz ◽  
Xin Lan ◽  
Audra McClure-Begley ◽  
Irina Petropavlovskikh ◽  
...  

This paper is aimed at atmospheric scientists without formal training in statistical theory. Its goal is to (1) provide a critical review of the rationale for trend analysis of the time series typically encountered in the field of atmospheric chemistry, (2) describe a range of trend-detection methods, and (3) demonstrate effective means of conveying the results to a general audience. Trend detections in atmospheric chemical composition data are often challenged by a variety of sources of uncertainty, which often behave differently to other environmental phenomena such as temperature, precipitation rate, or stream flow, and may require specific methods depending on the science questions to be addressed. Some sources of uncertainty can be explicitly included in the model specification, such as autocorrelation and seasonality, but some inherent uncertainties are difficult to quantify, such as data heterogeneity and measurement uncertainty due to the combined effect of short and long term natural variability, instrumental stability, and aggregation of data from sparse sampling frequency. Failure to account for these uncertainties might result in an inappropriate inference of the trends and their estimation errors. On the other hand, the variation in extreme events might be interesting for different scientific questions, for example, the frequency of extremely high surface ozone events and their relevance to human health. In this study we aim to (1) review trend detection methods for addressing different levels of data complexity in different chemical species, (2) demonstrate that the incorporation of scientifically interpretable covariates can outperform pure numerical curve fitting techniques in terms of uncertainty reduction and improved predictability, (3) illustrate the study of trends based on extreme quantiles that can provide insight beyond standard mean or median based trend estimates, and (4) present an advanced method of quantifying regional trends based on the inter-site correlations of multisite data. All demonstrations are based on time series of observed trace gases relevant to atmospheric chemistry, but the methods can be applied to other environmental data sets.


2017 ◽  
Vol 114 (10) ◽  
pp. 2491-2496 ◽  
Author(s):  
Lu Shen ◽  
Loretta J. Mickley

We develop a statistical model to predict June–July–August (JJA) daily maximum 8-h average (MDA8) ozone concentrations in the eastern United States based on large-scale climate patterns during the previous spring. We find that anomalously high JJA ozone in the East is correlated with these springtime patterns: warm tropical Atlantic and cold northeast Pacific sea surface temperatures (SSTs), as well as positive sea level pressure (SLP) anomalies over Hawaii and negative SLP anomalies over the Atlantic and North America. We then develop a linear regression model to predict JJA MDA8 ozone from 1980 to 2013, using the identified SST and SLP patterns from the previous spring. The model explains ∼45% of the variability in JJA MDA8 ozone concentrations and ∼30% variability in the number of JJA ozone episodes (>70 ppbv) when averaged over the eastern United States. This seasonal predictability results from large-scale ocean–atmosphere interactions. Warm tropical Atlantic SSTs can trigger diabatic heating in the atmosphere and influence the extratropical climate through stationary wave propagation, leading to greater subsidence, less precipitation, and higher temperatures in the East, which increases surface ozone concentrations there. Cooler SSTs in the northeast Pacific are also associated with more summertime heatwaves and high ozone in the East. On average, models participating in the Atmospheric Model Intercomparison Project fail to capture the influence of this ocean–atmosphere interaction on temperatures in the eastern United States, implying that such models would have difficulty simulating the interannual variability of surface ozone in this region.


2020 ◽  
Author(s):  
Meiyun Lin ◽  
Larry Horowitz ◽  
Yuanyu Xie ◽  
Fabien Paulot ◽  
Sergey Malyshev ◽  
...  

<p>This study highlights a previously under-appreciated “climate penalty” feedback mechanism - namely, substantial reductions of ozone uptake by water stressed vegetation – as a missing piece to the puzzle of why European ozone pollution episodes have not decreased as expected in recent decades, despite marked reductions in regional emissions of ozone precursors due to regulatory changes. The most extreme ozone pollution episodes are linked to heatwaves and droughts, which are increasing in frequency and intensity over Europe, with severe impacts on natural and human systems. Under drought stress, plants close their stomata to reduce water loss, consequently limiting the ozone uptake by vegetation (a component of dry deposition), leading to increased surface ozone concentrations. Such land-biosphere feedbacks are often overlooked in prior air quality projections, owing to a lack of process-based model formulations. Here, we use six decades of observations and Earth system model simulations (1960-2018) with an interactive dry deposition scheme to show that declining ozone removal by water-stressed vegetation in the warming climate exacerbate ozone air pollution over Europe. Incorporated into a dynamic vegetation land – atmospheric chemistry – climate model, the dry deposition scheme mechanistically describes the response of ozone deposition to atmospheric CO<sub>2 </sub>concentration, canopy air vapor pressure deficit, and soil water availability. Our observational and modeling analyses reveal drought stress causing as much as 70% reductions in ozone removal by forests. Reduced ozone removal by water-stressed vegetation worsens peak ozone episodes during European mega-droughts, such as the 2003 event, offsetting much of the air quality improvements gained from regional emission controls. Accounting for vegetation feedbacks leads to a three-fold increase in high surface ozone events above 80 ppbv (8-hour average) and a 20% increase in the sensitivity of ozone pollution extremes (95<sup>th </sup>percentile) to increasing temperature. As the frequency of hot and dry summers is expected to increase in the coming decades, this ozone climate penalty could be severe and therefore needs to be considered when designing clean air policy in the European Union. </p><p>Notes: This study is currently under review for possible publication in Nature Climate Change. </p>


2020 ◽  
Author(s):  
Minghu Ding ◽  
Biao Tian ◽  
Michael Ashley ◽  
Zhenxi Zhu ◽  
Lifan Wang ◽  
...  

Abstract. To evaluate the characteristics of near-surface O3 over Dome A (Kunlun Station), which is located at the summit of the east Antarctic Ice Sheet, continuous observations were carried out in 2016. Together with observations from the Amundsen–Scott Station (South Pole) and Zhongshan Station, the seasonal and diurnal O3 variabilities were investigated. The results showed different patterns between coastal and inland Antarctic areas that were characterized by high concentrations in cold seasons and at night. The annual mean values at the three stations were 29.19 ± 7.52 ppb, 29.94 ± 4.97 ppb and 24.06 ± 5.79 ppb. Then, specific atmospheric processes, including synoptic-scale air mass transport, were analysed by Hybrid Single-Particle Lagrangian Integrated Trajectory (HYSPLIT) back-trajectory analysis and the potential source contribution function (PSCF) model. Long-range transport was found to account for the O3 enhancement events (OEEs) during summer at Dome A, rather than efficient local production (consistent with previous studies in inland Antarctica). In addition, we observed OEEs during the polar night in the Dome A region, which was not previously found in Antarctica. To explain this unique finding, the occurrence of stratospheric intrusion (stratosphere-to-troposphere, STT) events was studied with the Stratosphere-to-Troposphere Exchange Flux (STEFLUX) tool. This finding suggested that STT events occurred frequently over Dome A and could account for 55 % of the total polar night period. The occurrence probability of OEEs agreed well with STT events, indicating that the STT process was the dominant factor affecting the near-surface O3 over Dome A in the absence of photochemical reaction sources during polar night. This work provides unique information on ozone variation at Dome A and expands our knowledge regarding such events in Antarctica.


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