scholarly journals Formaldehyde and nitrogen dioxide over the remote western Pacific Ocean: SCIAMACHY and GOME-2 validation using ship-based MAX-DOAS observations

2012 ◽  
Vol 12 (22) ◽  
pp. 11179-11197 ◽  
Author(s):  
E. Peters ◽  
F. Wittrock ◽  
K. Großmann ◽  
U. Frieß ◽  
A. Richter ◽  
...  

Abstract. In October 2009, shipborne Multi-Axis Differential Optical Absorption Spectroscopy (MAX-DOAS) measurements were performed during the TransBrom campaign over the western Pacific Ocean (≈ 40° N to 20° S). Vertical tropospheric trace gas columns and profiles of nitrogen dioxide (NO2) and formaldehyde (HCHO) as well as stratospheric NO2 columns were retrieved in order to validate corresponding measurements from the GOME-2 and SCIAMACHY satellite instruments and to estimate tropospheric background concentrations of these trace gases. All instruments reproduced the same characteristic, latitude-dependent shape of stratospheric NO2. SCIAMACHY and GOME-2 data differ by about 1% from each other while yielding lower vertical columns than MAX-DOAS morning values as a consequence of measurement time and stratospheric NO2 diurnal cycle. Due to this diurnal cycle, an increase of 8.7 ± 0.5 × 1013 molec cm−2 h−1 of stratospheric NO2 was estimated from MAX-DOAS data at low latitudes during the day. Tropospheric NO2 was above the detection limit only in regions of higher anthropogenic impact (ship traffic, transport of pollution from land). A background column of 1.3 × 1014 molec cm−2 (or roughly 50 ppt boundary layer concentration) can be estimated as upper limit for the remote ocean, which is in agreement with GOME-2 monthly mean values. In the marine boundary layer close to the islands of Hokkaido and Honshu, up to 0.8 ppbv were retrieved close to the surface. Background HCHO concentrations over the remote ocean exhibit a diurnal cycle with maximum values (depending strongly on weather conditions) of 4 × 1015 molec cm−2 for the vertical column at noontime. Corresponding peak concentrations of up to 1.1 ppbv were retrieved in elevated altitudes (≈ 400 m) around noon while maximum concentrations in the evening are close to the ground. An agreement between MAX-DOAS and GOME-2 data was found for typical vertical columns of 3 × 1015 molec cm−2 over the remote ocean at the time of overpass.

2012 ◽  
Vol 12 (6) ◽  
pp. 15977-16024 ◽  
Author(s):  
E. Peters ◽  
F. Wittrock ◽  
K. Großmann ◽  
U. Frieß ◽  
A. Richter ◽  
...  

Abstract. In October 2009, ship-borne Multi-Axis Differential Optical Absorption Spectroscopy (MAX-DOAS) measurements were performed during the TransBrom campaign over the Western Pacific Ocean (≈40° N to −207° S). Vertical tropospheric trace gas columns and profiles of nitrogen dioxide (NO2) and formaldehyde (HCHO) as well as stratospheric NO2 columns were retrieved in order to validate corresponding measurements from the GOME-2 and SCIAMACHY satellite instruments and to estimate tropospheric background concentrations of these trace gases. All instruments reproduced the same characteristic latitude-dependent shape of stratospheric NO2. SCIAMACHY and GOME-2 data differ by about 1% from each other while yielding lower vertical columns than MAX-DOAS morning values as a consequence of measurement time and stratospheric NO2 diurnal cycle. At low latitudes, an increase of 8.7 ± 0.5 × 1013 molec cm−2 h−1 of stratospheric NO2 was estimated from MAX-DOAS data. Tropospheric NO2 was above the detection limit only in regions of higher anthropogenic impact (ship traffic, transport of pollution from land). A background column of 1.3 × 1014 molec cm−2 (or roughly 50 ppt BL concentration) can be estimated as upper limit for the remote ocean, which is in agreement with GOME-2 monthly mean values. In the marine boundary layer close to the islands of Hokkaido and Honshu, up to 0.8 ppbv were retrieved close to the surface. Background HCHO concentrations over the remote ocean exhibit a diurnal cycle with maximum values (depending strongly on weather conditions) of 4 × 1015 molec cm−2 for the vertical column at noon-time. Corresponding peak concentrations of up to 1.1 ppbv were retrieved in altitudes of 400–600 m around noon while maximum concentrations in the evening are close to the ground. An agreement between MAX-DOAS and GOME-2 data was found for typical vertical columns of 3 × 1015 molec cm−2 over the remote ocean at the time of overpass.


2013 ◽  
Vol 13 (6) ◽  
pp. 3363-3378 ◽  
Author(s):  
K. Großmann ◽  
U. Frieß ◽  
E. Peters ◽  
F. Wittrock ◽  
J. Lampel ◽  
...  

Abstract. A latitudinal cross-section and vertical profiles of iodine monoxide (IO) are reported from the marine boundary layer of the Western Pacific. The measurements were taken using Multi-Axis Differential Optical Absorption Spectroscopy (MAX-DOAS) during the TransBrom cruise of the German research vessel Sonne, which led from Tomakomai, Japan (42° N, 141° E) through the Western Pacific to Townsville, Australia (19° S, 146° E) in October 2009. In the marine boundary layer within the tropics (between 20° N and 5° S), IO mixing ratios ranged between 1 and 2.2 ppt, whereas in the subtropics and at mid-latitudes typical IO mixing ratios were around 1 ppt in the daytime. The profile retrieval reveals that the bulk of the IO was located in the lower part of the marine boundary layer. Photochemical simulations indicate that the organic iodine precursors observed during the cruise (CH3I, CH2I2, CH2ClI, CH2BrI) are not sufficient to explain the measured IO mixing ratios. Reasonable agreement between measured and modelled IO can only be achieved if an additional sea-air flux of inorganic iodine (e.g., I2) is assumed in the model. Our observations add further evidence to previous studies that reactive iodine is an important oxidant in the marine boundary layer.


2012 ◽  
Vol 12 (10) ◽  
pp. 27475-27519 ◽  
Author(s):  
K. Großmann ◽  
U. Frieß ◽  
E. Peters ◽  
F. Wittrock ◽  
J. Lampel ◽  
...  

Abstract. A latitudinal cross-section and vertical profiles of iodine monoxide (IO) are reported from the marine boundary layer of the Western Pacific. The measurements were taken using Multi-Axis Differential Optical Absorption Spectroscopy (MAX-DOAS) during the TransBrom cruise of the German research vessel Sonne, which led from Tomakomai, Japan (42° N, 141° E) through the Western Pacific to Townsville, Australia (19° S, 146° E) in October 2009. In the marine boundary layer within the tropics (between 20° N and 5° S), IO mixing ratios ranged between 1 and 2.2 ppt, whereas in the subtropics and at mid-latitudes typical IO mixing ratios were around 1 ppt in the daytime. The profile retrieval reveals that the bulk of the IO was located in the lower part of the marine boundary layer. Photochemical simulations indicate that the organic iodine precursors observed during the cruise (CH3I, CH2I2, CH2ClI, CH2BrI) are not sufficient to explain the measured IO mixing ratios. Reasonable agreement between measured and modelled IO can only be achieved, if an additional sea-air flux of inorganic iodine (e.g. I2) is assumed in the model. Our observations add further evidence to previous studies that reactive iodine is an important oxidant in the marine boundary layer.


2021 ◽  
Author(s):  
Feng Xu ◽  
Shi‐Bo Yan ◽  
Hong‐Hai Zhang ◽  
Ying‐Cui Wu ◽  
Qian‐Yao Ma ◽  
...  

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