2014
DOI: 10.1002/asl2.489
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Evidence of a LNOX influence on middle/upper troposphere ozone‐mixing ratios at Dakar, Senegal during Northern Hemisphere summer season

Abstract: We present results for the vertical distribution of tropospheric ozone from 40 measurements at Dakar, Senegal (14.59• N, 17.5

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Cited by 5 publications
(9 citation statements)
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“…We show: (1) the WOOM's evolution is driven by episodic biomass burning plumes that are transported from Southern Africa in August and September; (2) polluted air from biomass burning can vary in height with ozone rich layers in the 2–5 km range; (3) easterly winds typically produce higher ozone mixing ratio values at Ascension Island, but we also observed higher ozone mixing ratios with westerly winds and back trajectories suggests a South American origin; (4) there is only limited evidence of the AEJ‐S in its strong phase (SJ) as would be expected based on results from Mari et al. (2008) and Adebiyi and Zuidema (2016); (5) high ozone mixing ratios are frequently observed in the 500–300 hPa layer, suggestive of a LNO X source from Africa which has been observed in similar layers and linked to LNO X near to and north of the Equator (Jenkins et al., 2008, 2012, 2014, 2015) and becomes more prominent during the last week in September and October in the observations; (6) the TEJ with its large anticyclonic circulation at 200 hPa is the dominant mechanism for cross‐equatorial transport of LNO X produced O 3 in the upper troposphere from West Africa to the South Tropical Atlantic Ocean.…”
Section: Discussionmentioning
confidence: 56%
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“…We show: (1) the WOOM's evolution is driven by episodic biomass burning plumes that are transported from Southern Africa in August and September; (2) polluted air from biomass burning can vary in height with ozone rich layers in the 2–5 km range; (3) easterly winds typically produce higher ozone mixing ratio values at Ascension Island, but we also observed higher ozone mixing ratios with westerly winds and back trajectories suggests a South American origin; (4) there is only limited evidence of the AEJ‐S in its strong phase (SJ) as would be expected based on results from Mari et al. (2008) and Adebiyi and Zuidema (2016); (5) high ozone mixing ratios are frequently observed in the 500–300 hPa layer, suggestive of a LNO X source from Africa which has been observed in similar layers and linked to LNO X near to and north of the Equator (Jenkins et al., 2008, 2012, 2014, 2015) and becomes more prominent during the last week in September and October in the observations; (6) the TEJ with its large anticyclonic circulation at 200 hPa is the dominant mechanism for cross‐equatorial transport of LNO X produced O 3 in the upper troposphere from West Africa to the South Tropical Atlantic Ocean.…”
Section: Discussionmentioning
confidence: 56%
“…(2006) show that lightning activity over Africa continues to enhance TOC values across the Southern Atlantic Ocean leading to the Tropical Ozone Paradox, where TOC values exceed those in the Northern Tropical Atlantic although biomass burning is active in West Africa. The pattern of elevated O 3 mixing ratios has also been found in Equatorial Africa (Jenkins et al., 2008) and the Northern Tropical Atlantic during the West African wet season where peaks in middle troposphere ozone mixing ratios are found downstream and at continental outflow regions of West Africa at Cape Verde and Dakar Senegal (Barret et al., 2010; Jenkins et al., 2012, 2014). Elevated middle troposphere O 3 mixing ratios at Barbados are observed downstream of tropical disturbances and linked to LNO X lightning (Jenkins et al., 2015).…”
Section: Introductionmentioning
confidence: 74%
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“…In addition, corona discharge in the vicinity of a lightning flash can also produce ozone directly (Bozem et al, 2014). Increase of O 3 concentration in the middle and upper troposphere associated with lightning and lightning produced NO x had been reported in many studies Zhang et al, 2012;Jenkins et al, 2014). However, influence of lightning and lightning induced NO x on O 3 concentration could be different in the atmospheric surface layer because of relatively more complex meteorological conditions and atmospheric chemical reactions.…”
Section: Introductionmentioning
confidence: 99%