scholarly journals Impact of forest fires, biogenic emissions and high temperatures on the elevated Eastern Mediterranean ozone levels during the hot summer of 2007

2012 ◽  
Vol 12 (18) ◽  
pp. 8727-8750 ◽  
Author(s):  
Ø. Hodnebrog ◽  
S. Solberg ◽  
F. Stordal ◽  
T. M. Svendby ◽  
D. Simpson ◽  
...  

Abstract. The hot summer of 2007 in southeast Europe has been studied using two regional atmospheric chemistry models; WRF-Chem and EMEP MSC-W. The region was struck by three heat waves and a number of forest fire episodes, greatly affecting air pollution levels. We have focused on ozone and its precursors using state-of-the-art inventories for anthropogenic, biogenic and forest fire emissions. The models have been evaluated against measurement data, and processes leading to ozone formation have been quantified. Heat wave episodes are projected to occur more frequently in a future climate, and therefore this study also makes a contribution to climate change impact research. The plume from the Greek forest fires in August 2007 is clearly seen in satellite observations of CO and NO2 columns, showing extreme levels of CO in and downwind of the fires. Model simulations reflect the location and influence of the fires relatively well, but the modelled magnitude of CO in the plume core is too low. Most likely, this is caused by underestimation of CO in the emission inventories, suggesting that the CO/NOx ratios of fire emissions should be re-assessed. Moreover, higher maximum values are seen in WRF-Chem than in EMEP MSC-W, presumably due to differences in plume rise altitudes as the first model emits a larger fraction of the fire emissions in the lowermost model layer. The model results are also in fairly good agreement with surface ozone measurements. Biogenic VOC emissions reacting with anthropogenic NOx emissions are calculated to contribute significantly to the levels of ozone in the region, but the magnitude and geographical distribution depend strongly on the model and biogenic emission module used. During the July and August heat waves, ozone levels increased substantially due to a combination of forest fire emissions and the effect of high temperatures. We found that the largest temperature impact on ozone was through the temperature dependence of the biogenic emissions, closely followed by the effect of reduced dry deposition caused by closing of the plants' stomata at very high temperatures. The impact of high temperatures on the ozone chemistry was much lower. The results suggest that forest fire emissions, and the temperature effect on biogenic emissions and dry deposition, will potentially lead to substantial ozone increases in a warmer climate.

2012 ◽  
Vol 12 (3) ◽  
pp. 7617-7675 ◽  
Author(s):  
Ø. Hodnebrog ◽  
S. Solberg ◽  
F. Stordal ◽  
T. M. Svendby ◽  
D. Simpson ◽  
...  

Abstract. The hot summer of 2007 in Southeast Europe has been studied using two regional atmospheric chemistry models; WRF-Chem and EMEP MSC-W. The region was struck by three heat waves and a number of forest fire episodes, greatly affecting air pollution levels. We have focused on ozone and its precursors using state-of-the-art inventories for anthropogenic, biogenic and forest fire emissions. The models have been evaluated against measurement data, and processes leading to ozone formation have been quantified. Heat wave episodes are projected to occur more frequently in a future climate, and therefore this study also makes a contribution to climate change research. The plume from the Greek forest fires in August 2007 is clearly seen in satellite observations of CO and NO2 columns, showing extreme levels of CO in and downwind of the fires. Model simulations reflect the location and influence of the fires relatively well, but the modelled magnitude of CO in the plume core is too low. Most likely, this is caused by underestimation of CO in the emission inventories, suggesting that the CO/NOx ratios of fire emissions should be re-assessed. Moreover, higher maximum values are seen in WRF-Chem than in EMEP MSC-W, presumably due to differences in plume rise altitudes as the first model emits a larger fraction of the fire emissions in the lowermost model layer. The model results are also in fairly good agreement with surface ozone measurements. Biogenic VOC emissions reacting with anthropogenic NOx emissions are calculated to contribute significantly to the levels of ozone in the region, but the magnitude and geographical distribution depend strongly on the model and biogenic emission module used. During the July and August heat waves, ozone levels increased substantially due to a combination of forest fire emissions and the effect of high temperatures. We found that the largest temperature impact on ozone was through the temperature dependence of the biogenic emissions, closely followed by the effect of decreased dry deposition. The impact of high temperatures on the ozone chemistry was much lower. The results suggest that forest fire emissions, and the temperature effect on biogenic emissions and dry deposition, will potentially lead to substantial ozone increases in a warmer climate.


2016 ◽  
Vol 16 (5) ◽  
pp. 3485-3497 ◽  
Author(s):  
Marcella Busilacchio ◽  
Piero Di Carlo ◽  
Eleonora Aruffo ◽  
Fabio Biancofiore ◽  
Cesare Dari Salisburgo ◽  
...  

Abstract. The observations collected during the BOReal forest fires on Tropospheric oxidants over the Atlantic using Aircraft and Satellites (BORTAS) campaign in summer 2011 over Canada are analysed to study the impact of forest fire emissions on the formation of ozone (O3) and total peroxy nitrates ∑PNs, ∑ROONO2). The suite of measurements on board the BAe-146 aircraft, deployed in this campaign, allows us to calculate the production of O3 and of  ∑PNs, a long-lived NOx reservoir whose concentration is supposed to be impacted by biomass burning emissions. In fire plumes, profiles of carbon monoxide (CO), which is a well-established tracer of pyrogenic emission, show concentration enhancements that are in strong correspondence with a significant increase of concentrations of ∑PNs, whereas minimal increase of the concentrations of O3 and NO2 is observed. The ∑PN and O3 productions have been calculated using the rate constants of the first- and second-order reactions of volatile organic compound (VOC) oxidation. The ∑PN and O3 productions have also been quantified by 0-D model simulation based on the Master Chemical Mechanism. Both methods show that in fire plumes the average production of ∑PNs and O3 are greater than in the background plumes, but the increase of ∑PN production is more pronounced than the O3 production. The average ∑PN production in fire plumes is from 7 to 12 times greater than in the background, whereas the average O3 production in fire plumes is from 2 to 5 times greater than in the background. These results suggest that, at least for boreal forest fires and for the measurements recorded during the BORTAS campaign, fire emissions impact both the oxidized NOy and O3,  but (1 ∑PN production is amplified significantly more than O3 production and (2) in the forest fire plumes the ratio between the O3 production and the ∑PN production is lower than the ratio evaluated in the background air masses, thus confirming that the role played by the ∑PNs produced during biomass burning is significant in the O3 budget. The implication of these observations is that fire emissions in some cases, for example boreal forest fires and in the conditions reported here, may influence more long-lived precursors of O3 than short-lived pollutants, which in turn can be transported and eventually diluted in a wide area.


2015 ◽  
Vol 15 (5) ◽  
pp. 6009-6040
Author(s):  
M. Busilacchio ◽  
P. Di Carlo ◽  
E. Aruffo ◽  
F. Biancofiore ◽  
C. D. Salisburgo ◽  
...  

Abstract. The observations collected during the BORTAS campaign in summer 2011 over Canada are analysed to study the impact of forest fire emissions on the formation of ozone (O3) and total peroxy nitrates (ΣPNs, ΣROONO2). The suite of measurements on board the BAe-146 aircraft, deployed in this campaign, allows us to calculate the production of O3 and of ΣPNs, a long lived O3 reservoir whose concentration is supposed to be impacted by biomass burning emissions. In fire plumes, profiles of carbon monoxide (CO), which is a well-established tracer of pyrogenic emission, show concentration enhancements that are in strong correspondence with a significant increase of ΣPNs concentrations, whereas minimal increase of the concentrations of O3 and NO2 are observed. In those fire plumes the average ΣPNs production is 12 times greater than in the background plumes, by contrast the average O3 production is only 5 times greater. These results suggest that, at least for boreal forest fires and for the measurements recorded during the BORTAS campaign, fire emissions impact both the oxidized NOy and O3, but: (1) ΣPNs production is affected significantly respect to the O3 production and (2) in the forest fire plumes the ratio between the ΣPNs production and the O3 production is lower than the ratio evaluated in the background air masses, thus confirming that the role played by the ΣPNs produced during biomass burning is significant in the O3 budget. These observations are consistent with elevated production of PAN and concurrent low production (or sometimes loss) of O3 observed in some another campaigns (i.e. ARCTAS-B) focused on forest fire emissions. Moreover our observations extend ARCTAS-B results since PAN is one of the compounds included in the ΣPNs family detected during BORTAS. The implication of these observations is that fire emissions in some cases, for example Boreal forest fires and in the conditions reported here, may influence more long lived precursors of O3 than short lived pollutants, which in turn can be transported and eventually diluted in a wide area. These observations provide additional indirect evidence that O3 production may be enhanced as plumes from forest fires age.


1993 ◽  
Vol 69 (3) ◽  
pp. 290-293 ◽  
Author(s):  
Brian J. Stocks

The looming possibility of global warming raises legitimate concerns for the future of the forest resource in Canada. While evidence of a global warming trend is not conclusive at this time, governments would be wise to anticipate, and begin planning for, such an eventuality. The forest fire business is likely to be affected both early and dramatically by any trend toward warmer and drier conditions in Canada, and fire managers should be aware that the future will likely require new and innovative thinking in forest fire management. This paper summarizes research activities currently underway to assess the impact of global warming on forest fires, and speculates on future fire management problems and strategies.


2020 ◽  
Vol 237 ◽  
pp. 03012
Author(s):  
Christoph Senff ◽  
Andrew Langford ◽  
Raul Alvarez ◽  
Tim Bonin ◽  
Alan Brewer ◽  
...  

Recently, two air quality campaigns were conducted in the southwestern United States to study the impact of transported ozone, stratospheric intrusions, and fire emissions on ground-level ozone concentrations. The California Baseline Ozone Transport Study (CABOTS) took place in May – August 2016 covering the central California coast and San Joaquin Valley, and the Fires, Asian, and Stratospheric Transport Las Vegas Ozone Study (FAST-LVOS) was conducted in the greater Las Vegas, Nevada area in May – June 2017. During these studies, nearly 1000 hours of ozone and aerosol profile data were collected with the NOAA TOPAZ lidar. A Doppler wind lidar and a radar wind profiler provided continuous observations of atmospheric turbulence, horizontal winds, and mixed layer height. These measurements allowed us to directly observe the degree to which ozone transport layers aloft were entrained into the boundary layer and to quantify the resulting impact on surface ozone levels. Mixed layer heights in the San Joaquin Valley during CABOTS were generally below 1 km above ground level (AGL), while boundary layer heights in Las Vegas during FAST-LVOS routinely exceeded 3 km AGL and occasionally reached up to 4.5 km AGL. Consequently, boundary layer entrainment was more often observed during FAST-LVOS, while most elevated ozone layers passed untapped over the San Joaquin Valley during CABOTS.


2019 ◽  
Author(s):  
Lang Wang ◽  
Amos P. K. Tai ◽  
Chi-Yung Tam ◽  
Mehliyar Sadiq ◽  
Peng Wang ◽  
...  

Abstract. Surface ozone (O3) is an important air pollutant and greenhouse gas. Land use and land cover (LULC) is one of the critical factors influencing ozone, in addition to anthropogenic emissions and climate. LULC change can on the one hand affect ozone biogeochemically, i.e., via dry deposition and biogenic emissions of volatile organic compounds (VOCs). LULC change can on the other hand alter regional- to large-scale climate through modifying albedo and evapotranspiration, which can lead to changes in surface temperature, hydrometeorology and atmospheric circulation that can ultimately impact ozone biogeophysically over local and remote areas. Such biogeophysical effects of LULC on ozone are largely understudied. This study investigates the individual and combined biogeophysical and biogeochemical effects of LULC on ozone, and explicitly examines the critical pathway for how LULC change impacts ozone pollution. A global coupled atmosphere–chemistry–land model is driven by projected LULC changes from the present day (2000) to future (2050) under RCP4.5 and RCP8.5 scenarios, focusing on the boreal summer. Results reveal that when considering biogeochemical effects only, surface ozone is predicted to have slight changes by up to 2 ppbv maximum in some areas due to LULC changes. It is primarily driven by changes in isoprene emission and dry deposition counteracting each other in shaping ozone. In contrast, when considering the integrated effect of LULC, ozone is more substantially altered by up to 6 ppbv over several regions, reflecting the importance of biogeophysical effects on ozone changes. Furthermore, large areas of these ozone changes are found over the regions without LULC changes where the biogeophysical effect is the only pathway for such changes. The mechanism is likely that LULC change induces a regional circulation response, in particular the formation of anomalous stationary high-pressure systems, shifting of moisture transport, and near-surface warming over the middle-to-high northern latitudes in boreal summer, owing to associated changes in albedo and surface energy budget. Such temperature changes then alter ozone substantially. We conclude that the biogeophysical effect of LULC is an important pathway for the influence of LULC change on ozone air quality over both local and remote regions, even in locations without significant LULC changes. Overlooking the impact of biogeophysical effect may cause evident underestimation of the impacts of LULC change on ozone pollution.


2004 ◽  
Vol 155 (7) ◽  
pp. 263-277 ◽  
Author(s):  
Marco Conedera ◽  
Gabriele Corti ◽  
Paolo Piccini ◽  
Daniele Ryser ◽  
Francesco Guerini ◽  
...  

The Southern Alps, in particular the Canton Ticino, is the region of Switzerland that is most affected by the phenomenon of forest fires. Therefore, the cantonal authorities are continually confronted with problems of prevention, fire fighting and mitigation of the effects of forest fires. In this article forest fire management in Canton Ticino is analyzed in historical terms, verifying in particular the impact of the methods used and the improvement of technology addressing the frequency of events and the extent of burned surfaces. In this way it has been possible to show how a few structural measures (better organization of fire fighting crews and equipment, introduction of aerial fire fighting techniques, electrification followed by construction of shelters along railway lines, etc.) have rather reduced the extent of burned surfaces, while legislative measures such as restrictions of open fires help to reduce the number of forest fires.


2021 ◽  
pp. 19-26
Author(s):  
Николай Петрович Копылов ◽  
Елена Юрьевна Сушкина ◽  
Александр Евгеньевич Кузнецов ◽  
Виктория Ивановна Новикова

Проведены экспериментальные исследования влияния лучистого теплообмена на переход верхового лесного пожара на постройки IV и V степеней огнестойкости. Лесной верховой пожар моделировался горением штабеля древесины с интенсивностью тепловыделения, близкой к интенсивности при реальных пожарах. Получена зависимость изменения плотности теплового потока от расстояния до кромки горения. Экспериментально определены температура воздуха с подветренной стороны пожара и плотность выпадения искр в зависимости от расстояния. Проверена эффективность защиты растворами ретардантов деревянных строений от возгорания при лучистом теплообмене между факелом пламени пожара и объектом защиты. Crown fires are the main threat of the combustion transfer from the forest to objects located in it. Fire services dealing with forest fires face the problem how to protect these objects from forest fires. It is proposed to treat the object with retardant solutions before a forest fire approaches. To assess the effectiveness of such tactics for fire protection of objects when exposed to a heat flow from the combustion front there were carried out experiments on large-scale crown fire models. A crown fire is simulated with a pile of wood with a heat release rate of ≈ 13 MW m. The wind is generated by fans, its speed is close to the speed at which a forest fire occurs. Measurements of the heat flux density, medium temperature, and the density of sparks falling downwind of the fire front at different distances and heights were carried out. Calculations were carried out to assess the impact of heat flow on buildings of IV-V degrees of fire resistance. The results obtained are compared with experimental data and they are in good agreement. There have been determined the distances from the fire front at which the fire protection with retardant solutions is effective for structures of IV-V fire resistance degrees at radiant heat exchange.


2016 ◽  
Vol 16 (1) ◽  
pp. 239-253 ◽  
Author(s):  
I. Lehtonen ◽  
A. Venäläinen ◽  
M. Kämäräinen ◽  
H. Peltola ◽  
H. Gregow

Abstract. The target of this work was to assess the impact of projected climate change on forest-fire activity in Finland with special emphasis on large-scale fires. In addition, we were particularly interested to examine the inter-model variability of the projected change of fire danger. For this purpose, we utilized fire statistics covering the period 1996–2014 and consisting of almost 20 000 forest fires, as well as daily meteorological data from five global climate models under representative concentration pathway RCP4.5 and RCP8.5 scenarios. The model data were statistically downscaled onto a high-resolution grid using the quantile-mapping method before performing the analysis. In examining the relationship between weather and fire danger, we applied the Canadian fire weather index (FWI) system. Our results suggest that the number of large forest fires may double or even triple during the present century. This would increase the risk that some of the fires could develop into real conflagrations which have become almost extinct in Finland due to active and efficient fire suppression. However, the results reveal substantial inter-model variability in the rate of the projected increase of forest-fire danger, emphasizing the large uncertainty related to the climate change signal in fire activity. We moreover showed that the majority of large fires in Finland occur within a relatively short period in May and June due to human activities and that FWI correlates poorer with the fire activity during this time of year than later in summer when lightning is a more important cause of fires.


2018 ◽  
Vol 18 (19) ◽  
pp. 14133-14148 ◽  
Author(s):  
Shan S. Zhou ◽  
Amos P. K. Tai ◽  
Shihan Sun ◽  
Mehliyar Sadiq ◽  
Colette L. Heald ◽  
...  

Abstract. Tropospheric ozone is an air pollutant that substantially harms vegetation and is also strongly dependent on various vegetation-mediated processes. The interdependence between ozone and vegetation may constitute feedback mechanisms that can alter ozone concentration itself but have not been considered in most studies to date. In this study we examine the importance of dynamic coupling between surface ozone and leaf area index (LAI) in shaping ozone air quality and vegetation. We first implement an empirical scheme for ozone damage on vegetation in the Community Land Model (CLM) and simulate the steady-state responses of LAI to long-term exposure to a range of prescribed ozone levels (from 0 to 100 ppb). We find that most plant functional types suffer a substantial decline in LAI as ozone level increases. Based on the CLM-simulated results, we develop and implement in the GEOS-Chem chemical transport model a parameterization that computes fractional changes in monthly LAI as a function of local mean ozone levels. By forcing LAI to respond to ozone concentrations on a monthly timescale, the model simulates ozone–LAI coupling dynamically via biogeochemical processes including biogenic volatile organic compound (VOC) emissions and dry deposition, without the complication from meteorological changes. We find that ozone-induced damage on LAI can lead to changes in ozone concentrations by −1.8 to +3 ppb in boreal summer, with a corresponding ozone feedback factor of −0.1 to +0.6 that represents an overall self-amplifying effect from ozone–LAI coupling. Substantially higher simulated ozone due to strong positive feedbacks is found in most tropical forests, mainly due to the ozone-induced reductions in LAI and dry deposition velocity, whereas reduced isoprene emission plays a lesser role in these low-NOx environments. In high-NOx regions such as the eastern US, Europe, and China, however, the feedback effect is much weaker and even negative in some regions, reflecting the compensating effects of reduced dry deposition and reduced isoprene emission (which reduces ozone in high-NOx environments). In remote, low-LAI regions, including most of the Southern Hemisphere, the ozone feedback is generally slightly negative due to the reduced transport of NOx–VOC reaction products that serve as NOx reservoirs. This study represents the first step to accounting for dynamic ozone–vegetation coupling in a chemical transport model with ramifications for a more realistic joint assessment of ozone air quality and ecosystem health.


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