scholarly journals Chemical characteristics assigned to trajectory clusters during the MINOS campaign

2003 ◽  
Vol 3 (2) ◽  
pp. 459-468 ◽  
Author(s):  
M. Traub ◽  
H. Fischer ◽  
M. de Reus ◽  
R. Kormann ◽  
H. Heland ◽  
...  

Abstract. During the Mediterranean Intensive Oxidant Study (MINOS) in August 2001 a total of 14 measurement flights were performed with the DLR Falcon jet aircraft from Heraklion, Crete. One objective of this campaign was to investigate the role of long-range transport of pollutants into the Mediterranean area. An analysis of 5-day back trajectories indicates that in the lower troposphere (0-4 km) air masses originated from eastern and western Europe, in the mid-troposphere (4-8 km) from the North Atlantic Ocean region and in the upper troposphere (8-14 km) from North Atlantic Ocean/North America (NANA) as well as South Asia. We allocated all back trajectories to clusters based on their ending height and source region. The mixing ratios of ozone, nitrogen oxide, total reactive oxidized nitrogen (NOy), formaldehyde, methanol, acetonitrile, acetone, peroxyacetyl nitrate (PAN), carbon dioxide, carbon monoxide and methane measured along the flight tracks are examined in relation to the different cluster trajectories. In the lower troposphere the mean trace gas mixing ratios of the eastern Europe cluster trajectories were significantly higher than those from western Europe. In the upper troposphere air from the NANA region seems to be influenced by the stratosphere, in addition, air masses were transported from South Asia, being influenced by strong convection in the Indian monsoon.

2003 ◽  
Vol 3 (1) ◽  
pp. 107-134 ◽  
Author(s):  
M. Traub ◽  
H. Fischer ◽  
M. de Reus ◽  
R. Kormann ◽  
J. Heland ◽  
...  

Abstract. During the Mediterranean Intensive Oxidant Study (MINOS) in August 2001 a total of 14 measurement flights were performed with the DLR Falcon aircraft from Heraklion, Crete. One objective of this campaign was to investigate the role of long-range transport of pollutants into the Mediterranean area. An analysis of 5-day back trajectories indicates that in the lower troposphere (0–4 km) air masses originated from eastern and western Europe, in the mid-troposphere (4–8 km) from the Atlantic Ocean region and in the upper troposphere (8–14 km) from North Artlantic Ocean/North America  (NAONA) as well as South Asia. We allocated all back trajectories to clusters based on their ending height and source region. The mixing ratios of ozone, nitrogen oxide, total reactive oxidized nitrogen (NOy), formaldehyde, methanol, acetonitrile, acetone, peroxyacetyl nitrate (PAN), carbon dioxide, carbon monoxide and methane measured along the flight tracks are examined in relation to the different cluster trajectories. In the lower troposphere the mean gas mixing ratios of the eastern Europe cluster trajectories were significantly higher than that from western Europe. Considering 2-day instead of 5-day trajectories the relative differences between the concentrations of these two clusters increased. In the upper troposphere relatively high concentrations of  O3 and NOy, combined with low CO of the NAONA trajectories indicate mixing with stratospheric air masses.


2016 ◽  
Author(s):  
X. W. Fu ◽  
N. Marusczak ◽  
L. -E. Heimbürger ◽  
B. Sauvage ◽  
F. Gheusi ◽  
...  

Abstract. Continuous measurements of atmospheric gaseous elemental mercury (GEM), particulate bound mercury (PBM) and gaseous oxidized mercury (GOM) at the high-altitude Pic du Midi Observatory (PDM, 2877 m a.s.l) in southern France were made from Nov 2011 to Nov 2012. The mean GEM, PBM and GOM concentrations were 1.86 ng m−3, 14 pg m−3 and 27 pg m−3, respectively and we observed 44 high PBM (up to 98 pg m−3) and 61 high GOM (up to 295 pg m−3) events. The high PBM events occurred mainly in cold seasons (winter and spring) whereas high GOM events were mainly observed in the warm seasons (summer and autumn). In cold seasons the maximum air mass residence times (ARTs) associated with high PBM events were observed in the upper troposphere over North America. The ratios of high PBM ARTs to total ARTs over North America, Europe, the Arctic region and Atlantic Ocean were all elevated in the cold season compared to the warm season, indicating that the middle and upper free troposphere of the Northern Hemisphere may be more enriched in PBM in cold seasons. PBM concentrations and PBM/GOM ratios during the high PBM events were significantly anti-correlated with atmospheric aerosol concentrations, air temperature and solar radiation, suggesting in situ formation of PBM in the middle and upper troposphere. We identified two distinct types of high GOM events with the GOM concentrations positively and negatively correlated with atmospheric ozone concentrations, respectively. High GOM events positively correlated with ozone were mainly related to air masses from the upper troposphere over the Arctic region and middle troposphere over the temperate North Atlantic Ocean, whereas high GOM events anti-correlated with ozone were mainly related to air masses from the lower free troposphere over the subtropical North Atlantic Ocean. The ARTs analysis demonstrates that the lower and middle free troposphere over the North Atlantic Ocean was the largest source region of atmospheric GOM at PDM Observatory. The ratios of high GOM ARTs to total ARTs over the subtropical North Atlantic Ocean in summer were significantly higher than that over the temperate and sub-arctic North Atlantic Ocean as well as that over the North Atlantic Ocean in other seasons, indicating abundant in situ oxidation of GEM to GOM in the lower free troposphere over the subtropical North Atlantic Ocean in summer.


2016 ◽  
Vol 16 (9) ◽  
pp. 5623-5639 ◽  
Author(s):  
Xuewu Fu ◽  
Nicolas Marusczak ◽  
Lars-Eric Heimbürger ◽  
Bastien Sauvage ◽  
François Gheusi ◽  
...  

Abstract. Continuous measurements of atmospheric gaseous elemental mercury (GEM), particulate bound mercury (PBM) and gaseous oxidized mercury (GOM) at the high-altitude Pic du Midi Observatory (PDM Observatory, 2877 m a.s.l.) in southern France were made from November 2011 to November 2012. The mean GEM, PBM and GOM concentrations were 1.86 ng m−3, 14 pg m−3 and 27 pg m−3, respectively and we observed 44 high PBM (peak PBM values of 33–98 pg m−3) and 61 high GOM (peak GOM values of 91–295 pg m−3) events. The high PBM events occurred mainly in cold seasons (winter and spring) whereas high GOM events were mainly observed in the warm seasons (summer and autumn). In cold seasons the maximum air mass residence times (ARTs) associated with high PBM events were observed in the upper troposphere over North America. The ratios of high PBM ARTs to total ARTs over North America, Europe, the Arctic region and Atlantic Ocean were all elevated in the cold season compared to the warm season, indicating that the middle and upper free troposphere of the Northern Hemisphere may be more enriched in PBM in cold seasons. PBM concentrations and PBM ∕ GOM ratios during the high PBM events were significantly anti-correlated with atmospheric aerosol concentrations, air temperature and solar radiation, suggesting in situ formation of PBM in the middle and upper troposphere. We identified two distinct types of high GOM events with the GOM concentrations positively and negatively correlated with atmospheric ozone concentrations, respectively. High GOM events positively correlated with ozone were mainly related to air masses from the upper troposphere over the Arctic region and middle troposphere over the temperate North Atlantic Ocean, whereas high GOM events anti-correlated with ozone were mainly related to air masses from the lower free troposphere over the subtropical North Atlantic Ocean. The ARTs analysis demonstrates that the lower and middle free troposphere over the North Atlantic Ocean was the largest source region of atmospheric GOM at the PDM Observatory. The ratios of high GOM ARTs to total ARTs over the subtropical North Atlantic Ocean in summer were significantly higher than those over the temperate and sub-arctic North Atlantic Ocean as well as that over the North Atlantic Ocean in other seasons, indicating abundant in situ oxidation of GEM to GOM in the lower free troposphere over the subtropical North Atlantic Ocean in summer.


2011 ◽  
Vol 11 (14) ◽  
pp. 7375-7397 ◽  
Author(s):  
S.-H. Lee ◽  
S.-W. Kim ◽  
M. Trainer ◽  
G. J. Frost ◽  
S. A. McKeen ◽  
...  

Abstract. Transport and chemical transformation of well-defined New York City (NYC) urban plumes over the North Atlantic Ocean were studied using aircraft measurements collected on 20–21 July 2004 during the ICARTT (International Consortium for Atmospheric Research on Transport and Transformation) field campaign and WRF-Chem (Weather Research and Forecasting-Chemistry) model simulations. The strong NYC urban plumes were characterized by carbon monoxide (CO) mixing ratios of 350–400 parts per billion by volume (ppbv) and ozone (O3) levels of about 100 ppbv near New York City on 20 July in the WP-3D in-situ and DC-3 lidar aircraft measurements. On 21 July, the two aircraft captured strong urban plumes with about 350 ppbv CO and over 150 ppbv O3 (~160 ppbv maximum) about 600 km downwind of NYC over the North Atlantic Ocean. The measured urban plumes extended vertically up to about 2 km near New York City, but shrank to 1–1.5 km over the stable marine boundary layer (MBL) over the North Atlantic Ocean. The WRF-Chem model reproduced ozone formation processes, chemical characteristics, and meteorology of the measured urban plumes near New York City (20 July) and in the far downwind region over the North Atlantic Ocean (21 July). The quasi-Lagrangian analysis of transport and chemical transformation of the simulated NYC urban plumes using WRF-Chem results showed that the pollutants can be efficiently transported in (isentropic) layers in the lower atmosphere (<2–3 km) over the North Atlantic Ocean while maintaining a dynamic vertical decoupling by cessation of turbulence in the stable MBL. The O3 mixing ratio in the NYC urban plumes remained at 80–90 ppbv during nocturnal transport over the stable MBL, then grew to over 100 ppbv by daytime oxidation of nitrogen oxides (NOx = NO + NO2) with mixing ratios on the order of 1 ppbv. Efficient transport of reactive nitrogen species (NOy), specifically nitric acid (HNO3), was confirmed through the comparison of the CO/NOy ratio in photochemically fresh and aged NYC plumes, implying the possibility of long-range transport of O3 over the stable MBL over the North Atlantic Ocean in association with NOx regeneration mechanism. The impact of chemical initial and boundary conditions (IC/BCs) on modelled O3 urban plumes was investigated in terms of the background O3 level and the vertical structure of the urban plumes. Simulations with dynamic ("time-variant") chemical IC/BCs enhanced the O3 level by 2–12 ppbv on average in the atmospheric layer below 3 km, showing better agreement with the observed NYC plumes and biomass-burning plumes than the simulation with prescribed static IC/BCs. The simulation including MOZART-4 chemical IC/BCs and Alaskan/Canadian wildfire emissions compared better to the observed O3 profiles in the upper atmospheric layer (>~3 km) than models that only accounted for North American anthropogenic/biogenic and wildfire contributions to background ozone. The comparison between models and observations show that chemical IC/BCs must be properly specified to achieve accurate model results.


2010 ◽  
Vol 10 (8) ◽  
pp. 3723-3741 ◽  
Author(s):  
J. Hegarty ◽  
H. Mao ◽  
R. Talbot

Abstract. The distributions of tropospheric ozone (O3) and carbon monoxide (CO), and the synoptic factors regulating these distributions over the western North Atlantic Ocean during winter and summer were investigated using profile retrievals from the Tropospheric Emission Spectrometer (TES) for 2004–2006. Seasonal composites of TES retrievals, reprocessed to remove the influence of the a priori on geographical and seasonal structure, exhibited strong seasonal differences. At the 681 hPa level during winter months of December, January and February (DJF) the composite O3 mixing ratios were uniformly low (~45 ppbv), but continental export was evident in a channel of enhanced CO (100–110 ppbv) flowing eastward from the US coast. In summer months June, July, and August (JJA) O3 mixing ratios were variable (45–65 ppbv) and generally higher due to increased photochemical production. The summer distribution also featured a channel of enhanced CO (95–105 ppbv) flowing northeastward around an anticyclone and exiting the continent over the Canadian Maritimes around 50° N. Offshore O3-CO slopes were generally 0.15–0.20 mol mol−1 in JJA, indicative of photochemical O3 production. Composites for 4 predominant synoptic patterns or map types in DJF suggested that export to the lower free troposphere (681 hPa level) was enhanced by the warm conveyor belt airstream of mid-latitude cyclones while stratospheric intrusions increased TES O3 levels at 316 hPa. A major finding in the DJF data was that offshore 681 hPa CO mixing ratios behind cold fronts could be enhanced up to >150 ppbv likely by lofting from the surface via shallow convection resulting from rapid destabilization of cold air flowing over much warmer ocean waters. In JJA composites for 3 map types showed that the general export pattern of the seasonal composites was associated with a synoptic pattern featuring the Bermuda High. However, weak cyclones and frontal troughs could enhance offshore 681 hPa CO mixing ratios to >110 ppbv with O3-CO slopes >0.50 mol mol−1 south of 45° N. Intense cyclones, which were not as common in the summer, enhanced export by lofting of boundary layer pollutants from over the US and also provided a possible mechanism for transporting pollutants from boreal fire outflow southward to the US east coast. Overall, for winter and summer the TES retrievals showed substantial evidence of air pollution export to the western North Atlantic Ocean with the most distinct differences in distribution patterns related to strong influences of mid-latitude cyclones in winter and the Bermuda High anticyclone in summer.


2017 ◽  
Vol 21 (3) ◽  
pp. 1397-1419 ◽  
Author(s):  
Monica Ionita ◽  
Lena M. Tallaksen ◽  
Daniel G. Kingston ◽  
James H. Stagge ◽  
Gregor Laaha ◽  
...  

Abstract. The summer drought of 2015 affected a large portion of continental Europe and was one of the most severe droughts in the region since summer 2003. The summer of 2015 was characterized by exceptionally high temperatures in many parts of central and eastern Europe, with daily maximum temperatures 2 °C higher than the seasonal mean (1971–2000) over most of western Europe, and more than 3 °C higher in the east. It was the hottest and climatologically driest summer over the 1950–2015 study period for an area stretching from the eastern Czech Republic to Ukraine. For Europe, as a whole, it is among the six hottest and driest summers since 1950. High evapotranspiration rates combined with a lack of precipitation affected soil moisture and vegetation and led to record low river flows in several major rivers, even beyond the drought-hit region. The 2015 drought developed rather rapidly over the Iberian Peninsula, France, southern Benelux and central Germany in May and reached peak intensity and spatial extent by August, affecting especially the eastern part of Europe. Over the summer period, there were four heat wave episodes, all associated with persistent blocking events. Upper-level atmospheric circulation over Europe was characterized by positive 500 hPa geopotential height anomalies flanked by a large negative anomaly to the north and west (i.e., over the central North Atlantic Ocean extending to northern Fennoscandia) and another center of positive geopotential height anomalies over Greenland and northern Canada. Simultaneously, the summer sea surface temperatures (SSTs) were characterized by large negative anomalies in the central North Atlantic Ocean and large positive anomalies in the Mediterranean basin. Composite analysis shows that the western Mediterranean SST is strongly related to the occurrence of dry and hot summers over the last 66 years (especially over the eastern part of Europe). The lagged relationship between the Mediterranean SST and summer drought conditions established in this study can provide valuable skill for the prediction of drought conditions over Europe on interannual to decadal timescales.


During the period 20-8 ka BP, movements of the polar front in the North Atlantic Ocean between the latitudes of Iceland and the Iberian peninsula greatly affected the climate of western Europe. During the Lateglacial, sea-surface temperature changes were particularly marked in the Bay of Biscay. Such migrations of the polar front, which have been shown to be time-transgressive, have been used to explain Lateglacial climatic events in northwestern Europe. A comparative study of Lateglacial and early Holocene records from lacustrine sites in northern and northwestern Spain and the Pyrenees confirms that the Lateglacial climatic amelioration was time-transgressive along the seaboard of western Europe, beginning 500-1000 years earlier in northwestern Spain than in the British Isles. This time-lag is further exaggerated in the vegetational response by migrational lags and edaphic factors. There are marked differences in the nature and chronology of Lateglacial plant successions, not only between southwest and northwest Europe, but particularly between sites in northwestern Spain, the coastal lowlands of the Pays Basque and the Pyrenees. Sites in northwestern Spain, including that of Sanabria Marsh, here published in detail for the first time, show the moderating climatic influence of the Atlantic Ocean throughout the Lateglacial. There, the climatic amelioration began early, perhaps before 14 ka b p . Deciduous oak forest had already begun to develop during Lateglacial times; this observation suggests that the perglacial refugia for these trees lay close to the maritime Atlantic coasts of Spain and Portugal, and not in the Pyrenees as some authors have proposed. After the onset of the Lateglacial climatic amelioration, pine and birch forest became widespread in the Pyrenees but oaks were very sparse or absent. Oak forest only developed there after lOkaBP in the early Holocene. The Younger Dryas episode of cooling can be detected, but only by a small expansion of herbaceous plant communities in some areas and with almost no lowering of the treeline. In contrast, Lateglacial conditions in the Pays Basque appear to have been cold and bleak. Even birch and pine forest was poorly developed and may have disappeared with the onset of the Younger Dryas cooling. Acid heathland with Empetrum and ericaceous plants then developed, to be replaced by oak-hazel forest in the early Holocene. Here, clearly, the influence of cold polar water conditions in the Bay of Biscay was very strong. Pollen diagrams from marine cores in the Bay of Biscay are also reviewed, but low sedimentation rates, bioturbation and differential transport and preservation of pollen make comparison with continental pollen diagrams difficult and correlation only possible in broad terms. Accurate vegetational interpretations are impossible. Palynologists working on archaeological cave and rock shelter sequences in southwest France and northern Spain have claimed to recognize, between 32 and 14 ka BP, a series of interstadial intervals with expansions of temperate trees. Careful consideration of pollen diagrams covering the purported Laugerie and Lascaux interstadials, said to occur between 16 and 20 ka BP (conventionally the maximum period of glacial advance of the last glacial stage), suggests that temperate pollen has percolated down through overlying deposits and been preserved in certain sedimentologically favourable beds. Although widely accepted by archaeologists, these interstadials appear to have no reality and must be rejected. There is no trace of them in the long lacustrine records of Les Echets (Beaulieu & Reille 1984) and Grande Pile (Woillard 1975, 1978). There is thus no good palynological record for 30-16 ka BP from south-west Europe, other than the long pollen sequence from Padul in southern Spain (Pons & Reille 1986).


2003 ◽  
Vol 3 (2) ◽  
pp. 1991-2026 ◽  
Author(s):  
J. Heland ◽  
H. Ziereis ◽  
H. Schlager ◽  
M. de Reus ◽  
M. Traub ◽  
...  

Abstract. We present mean altitude profiles of NOx, NOy, O3, and CO as measured by the DLR Falcon aircraft during the MINOS 2001 campaign over the Mediterranean in August 2001 and compare the data with results from other aircraft campaigns, namely the SIL 1996 (North Atlantic flight corridor), the POLINAT-2 (North Atlantic flight corridor), and the EXPORT 2000 (central Europe) campaigns. The MINOS NOy, O3, and CO mixing ratios in the free troposphere, especially between 4–8 km, are very similar to those measured during the EXPORT 2000 campaign. However, compared to the other campaigns the MINOS O3 and CO were significantly higher in the boundary layer, by about 20 ppbV and 50 ppbV, respectively. In the second part of the paper the D[O3]/D[NOy], D[O3]/D[CO], D[CO]/D[NOy], and D[NOx]/D[NOy] trace gas correlations were calculated for the MINOS 2001 campaign. It was found that, within the scatter of the data, the overall average altitude profiles of the correlations compared well with data from a literature survey. The analysis of the mean vertical correlation profiles as measured during MINOS 2001 does therefore not single out special meteorological conditions and air mass origins over the Mediterranean in summer but reflects a more general condition of the free troposphere in the northern hemisphere. Correlation analyses for single flights at different altitudes, however, unambiguously identify air masses influenced by the stratosphere, whereas pollution plumes could only be identified with the help of back trajectories.


2011 ◽  
Vol 11 (5) ◽  
pp. 14031-14089
Author(s):  
S.-H. Lee ◽  
S.-W. Kim ◽  
M. Trainer ◽  
G. J. Frost ◽  
S. A. McKeen ◽  
...  

Abstract. Transport and chemical transformation of well-defined New York City (NYC) urban plumes over the North Atlantic Ocean were studied using aircraft measurements collected on 20–21 July 2004 during the ICARTT (International Consortium for Atmospheric Research on Transport and Transformation) field campaign and WRF-Chem (Weather Research and Forecasting-Chemistry) model simulations. The strong NYC urban plumes were characterized by carbon monoxide (CO) mixing ratios of 350–400 parts per billion by volume (ppbv) and ozone (O3) levels of about 100 ppbv near New York City on 20 July in the WP-3D in-situ and DC-3 lidar aircraft measurements. On 21 July, the two aircraft captured strong urban plumes with about 350 ppbv CO and over 150 ppbv O3 (~160 ppbv maximum) about 600 km downwind of NYC over the North Atlantic Ocean. The measured urban plumes extended vertically up to about 2 km near New York City, but shrank to 1–1.5 km over the stable marine boundary layer (MBL) over the North Atlantic Ocean. The WRF-Chem model reproduced ozone formation processes, chemical characteristics, and meteorology of the measured urban plumes near New York City (20 July) and in the far downwind region over the North Atlantic Ocean (21 July). The quasi-Lagrangian analysis of transport and chemical transformation of the simulated NYC urban plumes using WRF-Chem results showed that the pollutants can be efficiently transported in (isentropic) layers in the lower atmosphere (<2–3 km) over the North Atlantic Ocean while maintaining a dynamic vertical decoupling by cessation of turbulence in the stable MBL. The O3 mixing ratio in the NYC urban plumes remained at 80–90 ppbv during nocturnal transport over the stable MBL, then grew to over 100 ppbv by daytime oxidation of nitrogen oxides (NOx = NO + NO2) with mixing ratios on the order of 1 ppbv. Efficient transport of reactive nitrogen species (NOy), specifically nitric acid (HNO3), was confirmed through the comparison of the CO/NOy ratio in photochemically fresh and aged NYC plumes, implying the possibility of long-range transport of O3 over the stable MBL over the North Atlantic Ocean in association with NOx regeneration mechanism. The impact of chemical initial and boundary conditions (IC/BCs) on modelled O3 urban plumes was investigated in terms of the background O3 level and the vertical structure of the urban plumes. Simulations with dynamic chemical IC/BCs enhanced the O3 level by 2–12 ppbv on average in the atmospheric layer below 3 km, showing better agreement with the observed NYC plumes and biomass-burning plumes than the simulation with prescribed static IC/BCs. The simulation including MOZART-4 chemical IC/BCs and Alaskan/Canadian wildfire emissions compared better to the observed O3 profiles in the upper atmospheric layer (>~3 km) than models that only accounted for North American anthropogenic/biogenic and wildfire contributions to background ozone. The comparison between models and observations show that chemical IC/BCs must be properly specified to achieve accurate model results.


Sign in / Sign up

Export Citation Format

Share Document