scholarly journals Characteristics of intercontinental transport of tropospheric ozone from Africa to Asia

2018 ◽  
Vol 18 (6) ◽  
pp. 4251-4276 ◽  
Author(s):  
Han Han ◽  
Jane Liu ◽  
Huiling Yuan ◽  
Bingliang Zhuang ◽  
Ye Zhu ◽  
...  

Abstract. In this study, we characterize the transport of ozone from Africa to Asia through the analysis of the simulations of a global chemical transport model, GEOS-Chem, from 1987 to 2006. The receptor region Asia is defined within 5–60∘ N and 60–145∘ E, while the source region Africa is within 35∘ S–15∘ N and 20∘ W–55∘ E and within 15–35∘ N and 20∘ W–30∘ E. The ozone generated in the African troposphere from both natural and anthropogenic sources is tracked through tagged ozone simulation. Combining this with analysis of trajectory simulations using the Hybrid Single-Particle Lagrangian Integrated Trajectory (HYSPLIT) model, we find that the upper branch of the Hadley cell connects with the subtropical westerlies in the Northern Hemisphere (NH) to form a primary transport pathway from Africa to Asia in the middle and upper troposphere throughout the year. The Somali jet that runs from eastern Africa near the equator to the Indian subcontinent in the lower troposphere is the second pathway that appears only in NH summer. The influence of African ozone mainly appears over Asia south of 40∘ N. The influence shows strong seasonality, varying with latitude, longitude, and altitude. In the Asian upper troposphere, imported African ozone is largest from March to May around 30∘ N (12–16 ppbv) and lowest during July–October around 10∘ N (∼ 2 ppbv). In the Asian middle and lower troposphere, imported African ozone peaks in NH winter between 20 and 25∘ N. Over 5–40∘ N, the mean fractional contribution of imported African ozone to the overall ozone concentrations in Asia is largest during NH winter in the middle troposphere (∼ 18 %) and lowest in NH summer throughout the tropospheric column (∼ 6 %). This seasonality mainly results from the collective effects of the ozone precursor emissions in Africa and meteorology and chemistry in Africa, in Asia and along the transport pathways. The seasonal swing of the Hadley circulation and subtropical westerlies along the primary transport pathway plays a dominant role in modulating the seasonality. There is more imported African ozone in the Asian upper troposphere in NH spring than in winter. This is likely due to more ozone in the NH African upper troposphere generated from biogenic and lightning NOx emissions in NH spring. The influence of African ozone on Asia appears larger in NH spring than in autumn. This can be attributed to both higher altitudes of the elevated ozone in Africa and stronger subtropical westerlies in NH spring. In NH summer, African ozone hardly reaches Asia because of the blocking by the Saharan High, Arabian High, and Tibetan High on the transport pathway in the middle and upper troposphere, in addition to the northward swing of the subtropical westerlies. The seasonal swings of the intertropical convergence zone (ITCZ) in Africa, coinciding with the geographic variations of the ozone precursor emissions, can further modulate the seasonality of the transport of African ozone, owing to the functions of the ITCZ in enhancing lightning NOx generation and uplifting ozone and ozone precursors to upper layers. The strength of the ITCZ in Africa is also found to be positively correlated with the interannual variation of the transport of African ozone to Asia in NH winter. Ozone from NH Africa makes up over 80 % of the total imported African ozone over Asia in most altitudes and seasons. The interhemispheric transport of ozone from southern hemispheric Africa (SHAF) is most evident in NH winter over the Asian upper troposphere and in NH summer over the Asian lower troposphere. The former case is associated with the primary transport pathway in NH winter, while the latter case is associated with the second transport pathway. The intensities of the ITCZ in Africa and the Somali jet can each explain ∼ 30 % of the interannual variations in the transport of ozone from SHAF to Asia in the two cases.

2011 ◽  
Vol 11 (12) ◽  
pp. 32423-32453
Author(s):  
L. Huang ◽  
R. Fu ◽  
J. H. Jiang ◽  
J. S. Wright ◽  
M. Luo

Abstract. Past studies have identified various pathways along which carbon monoxide (CO) in the tropical upper troposphere (UT) may have been transported from the surface. However, the roles that these transport pathways play in determining the locations and seasonality of CO in the tropical UT remain unclear. In particular, UT CO peaks during the spring and fall seasons when surface CO emission and deep atmospheric convection are moderate relative to those observed during winter and summer. We have developed a method to automate the identification of three pathways that transport CO to the UT, which makes joint use of several A-Train satellite measurements. We use this method to show that the locations and seasonality of the major UT CO centers in the tropics during 2007 were largely determined by local convective transport. On average, the "local convection" pathway, in which convection occurred within a fire region, transported significantly more CO to the UT than the "LT advection → convection" pathway, in which CO was advected within the lower troposphere from a fire region to a convective region prior to convection. To leading order, the seasonality of CO concentrations in the tropical UT followed the seasonality of the "local convection" transport pathway. The centers of highest CO peaked over Central Africa during boreal spring and over South America during austral spring, when the "local convection" transport pathway was most prevalent. During boreal winter and summer, surface CO emission and convection were located in opposite hemispheres, limiting the effectiveness of transport to the UT. In these seasons, CO was mainly transported to the UT via the "LT advection → convection" pathway, in which CO was advected within the lower troposphere from fire source regions in the winter hemisphere to convective regions in the summer hemisphere, or via the "UT advection" pathway, in which UT CO was redistributed from the summer hemisphere to the winter hemisphere.


2012 ◽  
Vol 12 (10) ◽  
pp. 4683-4698 ◽  
Author(s):  
L. Huang ◽  
R. Fu ◽  
J. H. Jiang ◽  
J. S. Wright ◽  
M. Luo

Abstract. Past studies have identified a variety of pathways by which carbon monoxide (CO) may be transported from the surface to the tropical upper troposphere (UT); however, the relative roles that these transport pathways play in determining the distribution and seasonality of CO in the tropical UT remain unclear. We have developed a method to automate the identification of two pathways ("local convection" and "advection within the lower troposphere (LT) followed by convective vertical transport") involved in CO transport from the surface to the UT. This method is based on the joint application of instantaneous along-track, co-located, A-Train satellite measurements. Using this method, we find that the locations and seasonality of the UT CO maxima in the tropics were strongly correlated with the frequency of local convective transport during 2007. We also find that the "local convection" pathway (convective transport that occurred within a fire region) typically transported significantly more CO to the UT than the "LT advection → convection" pathway (advection of CO within the LT from a fire region to a convective region prior to convective transport). To leading order, the seasonality of CO concentrations in the tropical UT reflected the seasonality of the "local convection" transport pathway during 2007. The UT CO maxima occurred over Central Africa during boreal spring and over South America during austral spring. Occurrence of the "local convection" transport pathway in these two regions also peaked during these seasons. During boreal winter and summer, surface CO emission and convection were located in opposite hemispheres, which limited the effectiveness of transport to the UT. During these seasons, CO transport from the surface to the UT typically occurred via the "LT advection → convection" pathway.


2011 ◽  
Vol 11 (24) ◽  
pp. 13395-13419 ◽  
Author(s):  
I. Bouarar ◽  
K. S. Law ◽  
M. Pham ◽  
C. Liousse ◽  
H. Schlager ◽  
...  

Abstract. A global chemistry-climate model LMDz_INCA is used to investigate the contribution of African and Asian emissions to tropospheric ozone over Central and West Africa during the summer monsoon. The model results show that ozone in this region is most sensitive to lightning NOx and to Central African biomass burning emissions. However, other emission categories also contribute significantly to regional ozone. The maximum ozone changes due to lightning NOx occur in the upper troposphere between 400 hPa and 200 hPa over West Africa and downwind over the Atlantic Ocean. Biomass burning emissions mainly influence ozone in the lower and middle troposphere over Central Africa, and downwind due to westward transport. Biogenic emissions of volatile organic compounds, which can be uplifted from the lower troposphere to higher altitudes by the deep convection that occurs over West Africa during the monsoon season, lead to maximum ozone changes in the lower stratosphere region. Soil NOx emissions over the Sahel region make a significant contribution to ozone in the lower troposphere. In addition, convective uplift of these emissions and subsequent ozone production are also an important source of ozone in the upper troposphere over West Africa. Concerning African anthropogenic emissions, they only make a small contribution to ozone compared to the other emission categories. The model results indicate that most ozone changes due to African emissions occur downwind, especially over the Atlantic Ocean, far from the emission regions. The import of Asian emissions also makes a considerable contribution to ozone concentrations above 150 hPa and has to be taken into account in studies of the ozone budget over Africa. Using IPCC AR5 (Intergovernmental Panel on Climate Change; Fifth Assessment Report) estimates of anthropogenic emissions for 2030 over Africa and Asia, model calculations show larger changes in ozone over Africa due to growth in Asian emissions compared to African emissions over the next 20 yr.


2013 ◽  
Vol 13 (10) ◽  
pp. 25567-25615
Author(s):  
L. Huang ◽  
R. Fu ◽  
J. H. Jiang

Abstract. Carbon monoxide (CO) is an important tracer to study the transport of fire-generated pollutants from the surface to the upper troposphere (UT). This study analyzed the relative importance of fire emission, convection and climate conditions on the interannual variation of CO in the tropical UT, by using satellite observations, reanalysis data and transport pathway auto-identification method developed in our previous study. Empirical orthogonal function (EOF) and singular value decomposition (SVD) methods are used to identify the dominant modes of CO interannual variation in the tropical UT and factors that are related to these modes. Results show that the leading EOF mode is dominated by CO anomalies over Indonesia related to El Niño-Southern Oscillation (ENSO). This is consistent with previous findings by directly evaluating CO anomaly field. Transport pathway analysis suggests that the differences of UT CO between different ENSO types over the tropical continents are mainly dominated by the "local convection" pathway, especially the average CO transported by this pathway. The relative frequency of the "advection within the lower troposphere (LT) followed by convective vertical transport" pathway appears to be responsible only for the UT CO differences over the west-central Pacific between El Niño and La Niña years.


2014 ◽  
Vol 7 (12) ◽  
pp. 12719-12733 ◽  
Author(s):  
F. Zus ◽  
G. Beyerle ◽  
S. Heise ◽  
T. Schmidt ◽  
J. Wickert

Abstract. The Global Positioning System (GPS) radio occultation (RO) technique provides valuable input for numerical weather prediction and is considered as a data source for climate related research. Numerous studies outline the high precision and accuracy of RO atmospheric soundings in the upper troposphere and lower stratosphere. In this altitude region (8–25 km) RO atmospheric soundings are considered to be free of any systematic error. In the tropical (30° S–30° N) Lower (<8 km) Troposphere (LT), this is not the case; systematic differences with respect to independent data sources exist and are still not completely understood. To date only little attention has been paid to the Open Loop (OL) Doppler model. Here we report on a RO experiment carried out on-board of the twin satellite configuration TerraSAR-X and TanDEM-X which possibly explains to some extent biases in the tropical LT. In two sessions we altered the OL Doppler model aboard TanDEM-X by not more than ±5 Hz with respect to TerraSAR-X and compare collocated atmospheric refractivity profiles. We find a systematic difference in the retrieved refractivity. The bias mainly stems from the tropical LT; there the bias reaches up to ±1%. Hence, we conclude that the negative bias (several Hz) of the OL Doppler model aboard TerraSAR-X introduces a negative bias (in addition to the negative bias which is primarily caused by critical refraction) in our retrieved refractivity in the tropical LT.


2007 ◽  
Vol 7 (20) ◽  
pp. 5357-5370 ◽  
Author(s):  
B. Sauvage ◽  
F. Gheusi ◽  
V. Thouret ◽  
J.-P. Cammas ◽  
J. Duron ◽  
...  

Abstract. A meso-scale model was used to understand and describe the dynamical processes driving high ozone concentrations observed during both dry and monsoon season in monthly climatologies profiles over Lagos (Nigeria, 6.6° N, 3.3° E), obtained with the MOZAIC airborne measurements (ozone and carbon monoxide). This study focuses on ozone enhancements observed in the upper-part of the lower troposphere, around 3000 m. Two individual cases have been selected in the MOZAIC dataset as being representative of the climatological ozone enhancements, to be simulated and analyzed with on-line Lagrangian backtracking of air masses. This study points out the role of baroclinic low-level circulations present in the Inter Tropical Front (ITF) area. Two low-level thermal cells around a zonal axis and below 2000 m, in mirror symmetry to each other with respect to equator, form near 20° E and around 5° N and 5° S during the (northern hemisphere) dry and wet seasons respectively. They are caused by surface gradients – the warm dry surface being located poleward of the ITF and the cooler wet surface equatorward of the ITF. A convergence line exists between the poleward low-level branch of each thermal cell and the equatorward low-level branch of the Hadley cell. Our main conclusion is to point out this line as a preferred location for fire products – among them ozone precursors – to be uplifted and injected into the lower free troposphere. The free tropospheric transport that occurs then depends on the hemisphere and season. In the NH dry season, the AEJ allows transport of ozone and precursors westward to Lagos. In the NH monsoon (wet) season, fire products are transported from the southern hemisphere to Lagos by the southeasterly trade that surmounts the monsoon layer. Additionally ozone precursors uplifted by wet convection in the ITCZ can also mix to the ones uplifted by the baroclinic cell and be advected up to Lagos by the trade flow.


2015 ◽  
Vol 15 (20) ◽  
pp. 11537-11555 ◽  
Author(s):  
D. Liu ◽  
B. Quennehen ◽  
E. Darbyshire ◽  
J. D. Allan ◽  
P. I. Williams ◽  
...  

Abstract. Black carbon aerosol (BC) deposited to the Arctic sea ice or present in the free troposphere can significantly affect the Earth's radiation budget at high latitudes yet the BC burden in these regions and the regional source contributions are poorly constrained. Aircraft measurements of aerosol composition in the European Arctic were conducted during the Aerosol–Cloud Coupling And Climate Interactions in the Arctic (ACCACIA) campaign in March 2013. Pollutant plumes were encountered throughout the lower to upper Arctic troposphere featuring enhancements in CO and aerosol mass loadings, which were chemically speciated into BC and non-refractory sulphate and organic matter. FLEXPART-WRF simulations have been performed to evaluate the likely contribution to the pollutants from regional ground sources. By combining up-to-date anthropogenic and open fire biomass burning (OBB) inventories, we have been able to compare the contributions made to the observed pollution layers from the sources of eastern/northern Asia (AS), Europe (EU) and North America (NA). Over 90 % of the contribution to the BC was shown to arise from non-OBB anthropogenic sources. AS sources were found to be the major contributor to the BC burden, increasing background BC loadings by a factor of 3–5 to 100.8 ± 48.4 ng sm−3 (in standard air m3 at 273.15 K and 1013.25 mbar) and 55.8 ± 22.4 ng sm−3 in the middle and upper troposphere respectively. AS plumes close to the tropopause (about 7.5–8 km) were also observed, with BC concentrations ranging from 55 to 73 ng sm−3, which will potentially have a significant radiative impact. EU sources influenced the middle troposphere with a BC mean concentration of 70.8 ± 39.1 ng sm−3 but made a minor contribution to the upper troposphere due to the relatively high latitude of the source region. The contribution of NA was shown to be much lower at all altitudes with BC mean concentration of 20 ng sm−3. The BC transported to the Arctic is mixed with a non-BC volume fraction representing between 90–95 % of the mass, and has a relatively uniform core size distribution with mass median diameter 190–210 nm and geometric standard deviation σg = 1.55–1.65 and this varied little across all source regions. It is estimated that 60–95 % of BC is scavenged between emission and receptor based on BC / ΔCO comparisons between source inventories and measurement. We show that during the springtime of 2013, the anthropogenic pollution particularly from sources in Asia, contributed significantly to BC across the European Arctic free troposphere. In contrast to previous studies, the contribution from open wildfires was minimal. Given that Asian pollution is likely to continue to rise over the coming years, it is likely that the radiative forcing in the Arctic will also continue to increase.


MAUSAM ◽  
2022 ◽  
Vol 53 (4) ◽  
pp. 503-514
Author(s):  
R. SURESH

The total ozone derived from TOVS data from NOAA 12 satellite through one step physical retrieval algorithm of  International TOVS Processing Package (ITPP) version 5.0 has been used to identify  its diurnal, monthly, latitudinal and longitudinal variability during 1998 over the domain Equator to 26° N / 60-100° E. The linkage of  maximum total ozone with warmer tropopause and lower stratosphere has been re-established. The colder upper tropospheric temperature which is normally associated with maximum ozone concentration throughout the year elsewhere in the world  has also been identified in this study but the relationship gets reversed during southwest  monsoon months(June-September) over the domain considered. The moisture  available in abundance in the lower troposphere gets precipitated due to the convective instability prevailing in the atmosphere during monsoon season and very little moisture is only available for vertical transport into the upper troposphere atop 500 hPa. The latent heat released by the  precipitation processes warms up the middle and upper atmosphere. The warm and dry upper troposphere could be the reason for less depletion of ozone in the upper troposphere during monsoonal  months and this is supported by the positive correlation coefficient prevailing in monsoon season between  total ozone and upper tropospheric (aloft 300 hPa) temperature. The warmness in middle and upper troposphere which is associated with less depletion and/or production of more  ozone in the upper troposphere may  perhaps contribute  for the  higher total ozone during monsoon months than in other seasons over peninsular Indian region.  The minimum concentration is observed during January (226 DU) over 6° N and the maximum (283DU) over 18° N during August. Longitudinal variability is less pronounced than the latitudinal variability.


2021 ◽  
Author(s):  
Victor Lannuque ◽  
Bastien Sauvage ◽  
Brice Barret ◽  
Hannah Clark ◽  
Gilles Athier ◽  
...  

Abstract. Between December 2005 and 2013, the In-service Aircraft for a Global Observing System (IAGOS) program produced almost daily in situ measurements of CO and O3 between Europe and southern Africa. IAGOS data combined with measurements from the IASI instrument onboard the Metop-A satellite (2008–2013) are used to characterize meridional distributions and seasonality of CO and O3 in the African upper troposphere (UT). The FLEXPART particle dispersion model and the SOFT-IO model which combines the FLEXPART model with CO emission inventories are used to explore the sources and origins of the observed transects of CO and O3. We focus our analysis on two main seasons: December to March (DJFM) and June to October (JJASO). These seasons have been defined according to the position of Intertropical Convergence Zone (ITCZ), determined using in situ measurements from IAGOS. During both seasons, the UT CO meridional transects are characterized by maximum mixing ratios located 10° from the position of the ITCZ above the dry regions inside the hemisphere of the strongest Hadley cell (132 to 165 ppb at 0–5° N in DJFM and 128 to 149 ppb at 3–7° S in JJASO), and decreasing values south- and north-ward. The O3 meridional transects are characterized by mixing ratio minima of ~ 42–54 ppb at the ITCZ (10–16° S in DJFM and 5–8° N in JJASO) framed by local maxima (~ 53–71 ppb) coincident with the wind shear zones North and South of the ITCZ. O3 gradients are strongest in the hemisphere of the strongest Hadley cell. IASI UT O3 distributions in DJFM have revealed that the maxima are a part of a crescent-shaped O3 plume above the Atlantic Ocean around the Gulf of Guinea. CO emitted at the surface is transported towards the ITCZ by the trade winds and then convectively uplifted. Once in the upper troposphere, CO enriched air masses are transported away from the ITCZ by the upper branches of the Hadley cells and accumulate within the zonal wind shear zones where the maximum CO mixing ratios are found. Anthropogenic and fires both contribute, by the same order of magnitude, to the CO budget of the African upper troposphere. Local fires have the highest contribution, drive the location of the observed UT CO maxima, and are related to the following transport pathway: CO emitted at the surface is transported towards the ITCZ by the trade winds and further convectively uplifted. Then UT CO enriched air masses are transported away from the ITCZ by the upper branches of the Hadley cells and accumulate within the zonal wind shear zones where the maxima are located. Anthropogenic CO contribution is mostly from Africa during the entire year, with a low seasonal variability, and is related to similar transport circulation than fire air masses. There is also a large contribution from Asia in JJASO related to the fast convective uplift of polluted air masses in the Asian monsoon region which are further westward transported by the tropical easterly jet (TEJ) and the Asian monsoon anticyclone (AMA). O3 minima correspond to air masses that were recently uplifted from the surface where mixing ratios are low at the ITCZ. The O3 maxima correspond to old high altitude air masses uplifted from either local or long distance area of high O3 precursor emissions (Africa and South America during all the year, South Asia mainly in JJASO), and must be created during transport by photochemistry. This analysis of meridional transects contribute to a better understanding of distributions of CO and O3 in the intertropical African upper troposphere and the processes which drive these distributions. Therefore, it provides a solid basis for comparison and improvement of models and satellite products in order to get the good O3 for the good reasons.


Author(s):  
Yuya Hamaguchi ◽  
Yukari N. Takayabu

AbstractIn this study, the statistical relationship between tropical upper-tropospheric troughs (TUTTs) and the initiation of summertime tropical-depression type disturbances (TDDs) over the western and central North Pacific is investigated. By applying a spatiotemporal filter to the 34-year record of brightness temperature and using JRA-55 reanalysis products, TDD-event initiations are detected and classified as trough-related (TR) or non-trough-related (non-TR). The conventional understanding is that TDDs originate primarily in the lower-troposphere; our results refine this view by revealing that approximately 30% of TDDs in the 10°N-20°N latitude ranges are generated under the influence of TUTTs. Lead-lag composite analysis of both TR- and non-TR-TDDs clarifies that TR-TDDs occur under relatively dry and less convergent large-scale conditions in the lower-troposphere. This result suggests that TR-TDDs can form in a relatively unfavorable low-level environment. The three-dimensional structure of the wave activity flux reveals southward and downward propagation of wave energy in the upper troposphere that converges at the mid-troposphere around the region where TR-TDDs occur, suggesting the existence of extratropical forcing. Further, the role of dynamic forcing associated with the TUTT on the TR-TDD-initiation is analyzed using the quasi-geostrophic omega equation. The result reveals that moistening in the mid-to-upper troposphere takes place in association with the sustained dynamical ascent at the southeast side of the TUTT, which precedes the occurrence of deep convective heating. Along with a higher convective available potential energy due to the destabilizing effect of TUTTs, the moistening in the mid-to-upper troposphere also helps to prepare the environment favorable to TDDs initiation.


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