scholarly journals Characteristics of Ethiopia Air Chemistry and Its Meteorological Context

2018 ◽  
Vol 22 (12) ◽  
pp. 1-22 ◽  
Author(s):  
Mark R. Jury

Abstract The concentration of trace gases and aerosols in Ethiopia is poorly characterized due to a limited history of surface measurements. Here, satellite measurements and model estimates of atmospheric composition are employed to understand space–time distributions in the period 2000–16. Methane (CH4) and carbon monoxide (CO) display high concentrations over the highlands and provide a focus for analysis of monthly and daily data. CH4 emissions from livestock peak at the beginning of the dry season, while CO from biomass burning rises at the end of the dry season. The seasonal cycle of dust, aerosol optical depth (AOD), and CO2 is inversely related with CH4, while CO closely follows sensible heat flux, thus linking drying and rural biomass burning. Stable easterly flow in the dry season accumulates local emissions, so near-surface concentrations of CO and CH4 are high then. The weather pattern underlying an episode of high nitrogen dioxide (NO2) concentrations was studied. In addition to a stable lapse rate and dry anticyclonic weather, midtropospheric subsidence was related to intrusion of the northern subtropical jet stream on 24–26 December 2010. The wind shadow was cast by the Rift Escarpment limited dispersion, particularly with the dry, stable weather conditions. A key outcome of this work is that CH4 concentrations over Ethiopia are high in global context and have increased >0.1 ppm from 2002 to 2016; hence, there is a need to improve livestock management and production efficiency.

1985 ◽  
Vol 15 (1-2) ◽  
pp. 77-120 ◽  
Author(s):  
P.J. Crutzen ◽  
M.T. Coffey ◽  
A.C. Delany ◽  
J. Greenberg ◽  
P. Haagenson ◽  
...  

Field measurement programs in Brazil during the dry season months of August and September in 1979 and 1980 have demonstrated the great importance of the continental tropics in global air chemistry. Especially in the mixed layer, the air composition over land is much different from that over the ocean and the land areas are clearly longe scale sources of many inportant trace gases. During the dry season much biomass, burning takes place especially in the cerrado regions leading to substantial emission of air pollutants, such as CO, NOx, N2O, CH4 and other hydrocarbons. Ozone concentrations are alsoenhanced due to photochemical reactions. Biogenic organic emissions from tropical forests play likewise an important role in the photochemistry of the atmosphere. Carbon monoxide was found to be present in high concentrations in the boundary layer of the tropical forest, but ozone concentrations were much lower than in the cerrado.


2020 ◽  
Author(s):  
Margaret Marvin ◽  
Paul Palmer ◽  
Fei Yao ◽  
Barry Latter ◽  
Richard Siddans ◽  
...  

<p>Mainland and maritime Southeast Asia is home to more than 655 million people, representing nearly 10% of the global population. The dry season in this region is typically associated with intense biomass burning activity, which leads to a significant increase in surface air pollutants that are harmful to human health, including ozone (O<sub>3</sub>) and fine (radii smaller than 2.5 microns) particulate matter (PM<sub>2.5</sub>). Latitude-based differences in dry season timing and land use distinguish two regional biomass burning regimes: (1) agricultural waste burning on the peninsular mainland from February through April and (2) coastal peat burning across the equatorial islands in September and October. The type and amount of material burned determines the chemical composition of emissions and subsequently their impact on regional air quality. Understanding the individual and collective roles of these biomass burning regimes is a crucial step towards developing effective air quality mitigation strategies for Southeast Asia. Here, we use the nested GEOS-Chem atmospheric chemistry transport model (horizontal resolution of 0.25° x 0.3125°) to simulate fire-atmosphere interactions over Southeast Asia during March and September of 2014, when emissions peak from the two regional burning seasons. Based on our analysis of model output, we report how these two distinct biomass burning regimes impact the photochemical environment over Southeast Asia and what the resulting consequences are for surface air quality. We will also present a critical evaluation of our model using ground-based and satellite observations of atmospheric composition across the region.</p>


2016 ◽  
Vol 16 (15) ◽  
pp. 9727-9743 ◽  
Author(s):  
James D. Whitehead ◽  
Eoghan Darbyshire ◽  
Joel Brito ◽  
Henrique M. J. Barbosa ◽  
Ian Crawford ◽  
...  

Abstract. The Amazon basin is a vast continental area in which atmospheric composition is relatively unaffected by anthropogenic aerosol particles. Understanding the properties of the natural biogenic aerosol particles over the Amazon rainforest is key to understanding their influence on regional and global climate. While there have been a number of studies during the wet season, and of biomass burning particles in the dry season, there has been relatively little work on the transition period – the start of the dry season in the absence of biomass burning. As part of the Brazil–UK Network for Investigation of Amazonian Atmospheric Composition and Impacts on Climate (BUNIAACIC) project, aerosol measurements, focussing on unpolluted biogenic air masses, were conducted at a remote rainforest site in the central Amazon during the transition from wet to dry season in July 2013. This period marks the start of the dry season but before significant biomass burning occurs in the region. Median particle number concentrations were 266 cm−3, with size distributions dominated by an accumulation mode of 130–150 nm. During periods of low particle counts, a smaller Aitken mode could also be seen around 80 nm. While the concentrations were similar in magnitude to those seen during the wet season, the size distributions suggest an enhancement in the accumulation mode compared to the wet season, but not yet to the extent seen later in the dry season, when significant biomass burning takes place. Submicron nonrefractory aerosol composition, as measured by an aerosol chemical speciation monitor (ACSM), was dominated by organic material (around 81 %). Aerosol hygroscopicity was probed using measurements from a hygroscopicity tandem differential mobility analyser (HTDMA), and a quasi-monodisperse cloud condensation nuclei counter (CCNc). The hygroscopicity parameter, κ, was found to be low, ranging from 0.12 for Aitken-mode particles to 0.18 for accumulation-mode particles. This was consistent with previous studies in the region, but lower than similar measurements conducted in Borneo, where κ ranged 0.17–0.37. A wide issue bioaerosol sensor (WIBS-3M) was deployed at ground level to probe the coarse mode, detecting primary biological aerosol by fluorescence (fluorescent biological aerosol particles, or FBAPs). The mean FBAP number concentration was 400 ± 242 L−1; however, this ranged from around 200 L−1 during the day to as much as 1200 L−1 at night. FBAPs dominated the coarse-mode particles, comprising between 55 and 75 % of particles during the day to more than 90 % at night. Non-FBAPs did not show a strong diurnal pattern. Comparison with previous FBAP measurements above canopy at the same location suggests there is a strong vertical gradient in FBAP concentrations through the canopy. Cluster analysis of the data suggests that FBAPs were dominated (around 70 %) by fungal spores. Further, long-term measurements will be required in order to fully examine the seasonal variability and distribution of primary biological aerosol particles through the canopy. This is the first time that such a suite of measurements has been deployed at this site to investigate the chemical composition and properties of the biogenic contributions to Amazonian aerosol during the transition period from the wet to the dry season, and thus provides a unique comparison to the aerosol properties observed during the wet season in previous similar campaigns. This was also the first deployment of a WIBS in the Amazon rainforest to study coarse-mode particles, particularly primary biological aerosol particles, which are likely to play an important role as ice nuclei in the region.


2009 ◽  
Vol 9 (20) ◽  
pp. 8017-8038 ◽  
Author(s):  
S.-W. Kim ◽  
P. Chazette ◽  
F. Dulac ◽  
J. Sanak ◽  
B. Johnson ◽  
...  

Abstract. We present observations of tropospheric aerosol and water vapor transport over West Africa and the associated meteorological conditions during the AMMA SOP-0 dry season experiment, which was conducted in West Africa in January–February 2006. This study combines data from ultra-light aircraft (ULA)-based lidar, airborne in-situ aerosol and gas measurements, standard meteorological measurements, satellite-based aerosol measurements, airmass trajectories, and radiosonde measurements. At Niamey (13.5° N, 2.2° E) the prevailing surface wind (i.e. Harmattan) was from the northeast bringing dry dusty air from the Sahara desert. High concentrations of mineral dust aerosol were typically observed from the surface to 1.5 or 2 km associated with the Saharan airmasses. At higher altitudes the prevailing wind veered to the south or southeast bringing relatively warm and humid airmasses from the biomass burning regions to the Sahel (<10° N). These elevated layers had high concentrations of biomass burning aerosol and were typically observed between altitudes of 2–5 km. Meteorological analyses show these airmasses were advected upwards over the biomass burning regions through ascent in Inter-Tropical Discontinuity (ITD) zone. Aerosol vertical profiles obtained from the space-based lidar CALIOP onboard CALIPSO during January 2007 also showed the presence of dust particles (particle depolarization (δ)~30%, lidar Ångström exponent (LAE)<0, aerosol backscatter to extinction ratio (BER): 0.026~0.028 sr−1) at low levels (<1.5 km) and biomass burning smoke aerosol (δ<10%, LAE: 0.6~1.1, BER: 0.015~0.018 sr−1) between 2 and 5 km. CALIOP data indicated that these distinct continental dust and biomass burning aerosol layers likely mixed as they advected further south over the tropical Atlantic Ocean, as indicated an intermediate values of δ (10~17%), LAE (0.16~0.18) and BER (0.0021~0.0022 sr−1).


2009 ◽  
Vol 9 (1) ◽  
pp. 1831-1871
Author(s):  
S.-W. Kim ◽  
P. Chazette ◽  
F. Dulac ◽  
J. Sanak ◽  
B. Johnson ◽  
...  

Abstract. We present observations of tropospheric aerosol and water vapor transport over West Africa and the associated meteorological conditions during the AMMA SOP-0 dry season experiment, which was conducted in West Africa in January–February 2006. This study combines data from ultra-light aircraft (ULA)-based lidar, airborne in-situ aerosol and gas measurements, standard meteorological measurements, satellite-based aerosol measurements, airmass trajectories, and radiosonde measurements. At Niamey (13.5° N, 2.2° E) the prevailing surface wind was from the northeast bringing dry dusty air from the Sahara desert. High concentrations of mineral dust aerosol were typically observed from the surface to 1.5 or 2 km associated with the Saharan airmasses. At higher altitudes the prevailing wind veered to the south or southeast bringing relatively warm and humid airmasses from the biomass burning regions to the Sahel (<10° N). These elevated layers had high concentrations of biomass burning aerosol and were typically observed between altitudes of 2–5 km. Meteorological analyses show these airmasses were advected upwards over the biomass burning regions through large-scale ascent, presumably driven by surface heating rather than pyro-convection. Aerosol vertical profiles obtained from the space-based lidar CALIOP onboard CALIPSO during January 2007 also showed the presence of dust particles (depolarization ~30%, color ratio <0) at low levels (<1.5 km) and biomass burning smoke aerosol (depolarization ratio <10%) between 2 and 5 km. CALIOP data indicated that these distinct continental dust and biomass burning aerosol layers likely mixed as they advected further south over the tropical Atlantic Ocean.


2016 ◽  
Author(s):  
J. D. Whitehead ◽  
E. Darbyshire ◽  
J. Brito ◽  
H. M. J. Barbosa ◽  
I. Crawford ◽  
...  

Abstract. The Amazon basin is a vast continental area in which atmospheric composition is relatively unaffected by anthropogenic aerosol particles. Understanding the properties of the natural biogenic aerosol particles over the Amazon rainforest is key to understanding their influence on regional and global climate. While there have been a number of studies during the wet season, and of biomass burning particles in the dry season, there has been relatively little work on the transition period – the start of the dry season in the absence of biomass burning. As part of the Brazil-UK Network for Investigation of Amazonian Atmospheric Composition and Impacts on Climate (BUNIAACIC) project, aerosol measurements, focussing on unpolluted biogenic air masses, were conducted above the canopy at a remote rainforest site in the Amazon, during the transition from wet to dry seasons, in July, 2013. This period marks the start of the dry season, but before significant biomass burning occurs in the region. Median particle number concentrations were 266 cm−3, with size distributions dominated by an accumulation mode of 130–150 nm. During periods of low particle counts, a smaller Aitken mode could also be seen around 80 nm. While the concentrations were similar in magnitude to those seen during the wet season, the size distributions suggest an enhancement in the accumulation mode compared to the wet season, but not yet to the extent seen later in the dry season, when significant biomass burning takes place. Submicron non-refractory aerosol composition, as measured by an Aerosol Chemical Speciation Monitor (ACSM), was dominated by organic material (86 %). Aerosol hygroscopicity was probed using measurements from a Hygroscopicity Tandem Differential Mobility Analyser (HTDMA), and a quasi-monodisperse Cloud Condensation Nuclei counter (CCNc). The hygroscopicity parameter, κ, was found to be low, ranging from 0.12 for Aitken mode particles to 0.18 for accumulation mode particles. This was consistent with previous studies in the region, but lower than similar measurements conducted in Borneo, where κ ranged 0.17–0.37, possibly due to a stronger marine influence at that location, bringing higher sulphate loadings than are typically seen in the Amazon. A Wide Issue Bioaerosol Sensor (WIBS-3M) was deployed at ground level to probe the coarse mode, detecting primary biological aerosol by fluorescence (Fluorescent Biological Aerosol Particles, or FBAP). The mean FBAP number concentration was 404 ± 237 l−1, however this was subject to a strong diurnal cycle, and ranged from around 200 l−1 during the day to as much as 1200 l−1 at night. FBAP dominated the coarse mode particles, comprising more than 90 % of particles detected by the WIBS-3 during the night. This proportion was also subject to a diurnal cycle, dropping to between 55 % and 75 % during the day, since non-FBAP did not show a strong diurnal pattern. Comparison with previous FBAP measurements above canopy at the same location suggests there is a strong vertical gradient in FBAP concentrations through the canopy. Application of Ward linkage cluster analysis using the z-score normalisation to the data suggests that FBAP were dominated (around 70 %) by fungal spores. Further, long-term measurements will be required in order to fully examine the seasonal variability, and distribution through the canopy of primary biological aerosol particles. This is the first time that such a suite of measurements has been deployed at this site to investigate the chemical composition and properties of the biogenic contributions to Amazonian aerosol during the transition period from the wet to dry seasons, and thus provides a unique contrast to the aerosol properties observed during the wet season in previous, similar campaigns. This was also the first deployment of a WIBS in the Amazon rainforest to study coarse mode particles, particularly primary biological aerosol particles, which is likely to play an important role as ice nuclei in the region.


Author(s):  
Milena Ponczek ◽  
Marco Aurélio de Menezes Franco ◽  
Samara Carbone ◽  
Luciana Varanda Rizzo ◽  
Djacinto Aparecido Monteiro dos Santos ◽  
...  

Biomass burning emissions in Amazonia changes the atmospheric composition and aerosol properties during the dry season. We investigated fine-mode aerosol chemical composition and optical properties at an intensive field experiment...


2021 ◽  
Vol 13 (10) ◽  
pp. 2001
Author(s):  
Antonella Boselli ◽  
Alessia Sannino ◽  
Mariagrazia D’Emilio ◽  
Xuan Wang ◽  
Salvatore Amoruso

During the summer of 2017, multiple huge fires occurred on Mount Vesuvius (Italy), dispersing a large quantity of ash in the surrounding area ensuing the burning of tens of hectares of Mediterranean scrub. The fires affected a very large area of the Vesuvius National Park and the smoke was driven by winds towards the city of Naples, causing daily peak values of particulate matter (PM) concentrations at ground level higher than the limit of the EU air quality directive. The smoke plume spreading over the area of Naples in this period was characterized by active (lidar) and passive (sun photometer) remote sensing as well as near-surface (optical particle counter) observational techniques. The measurements allowed us to follow both the PM variation at ground level and the vertical profile of fresh biomass burning aerosol as well as to analyze the optical and microphysical properties. The results evidenced the presence of a layer of fine mode aerosol with large mean values of optical depth (AOD > 0.25) and Ångstrom exponent (γ > 1.5) above the observational site. Moreover, the lidar ratio and aerosol linear depolarization obtained from the lidar observations were about 40 sr and 4%, respectively, consistent with the presence of biomass burning aerosol in the atmosphere.


2019 ◽  
Author(s):  
Yunjiang Zhang ◽  
Olivier Favez ◽  
Jean-Eudes Petit ◽  
Francesco Canonaco ◽  
Francois Truong ◽  
...  

Abstract. Organic aerosol (OA) particles are recognized as key factors influencing air quality and climate change. However, highly-time resolved year-round characterizations of their composition and sources in ambient air are still very limited due to challenging continuous observations. Here, we present an analysis of long-term variability of submicron OA using the combination of Aerosol Chemical Speciation Monitor (ACSM) and multi-wavelength aethalometer from November 2011 to March 2018 at a background site of the Paris region (France). Source apportionment of OA was achieved via partially constrained positive matrix factorization (PMF) using the multilinear engine (ME-2). Two primary OA (POA) and two oxygenated OA (OOA) factors were identified and quantified over the entire studied period. POA factors were designated as hydrocarbon-like OA (HOA) and biomass burning OA (BBOA). The latter factor presented a significant seasonality with higher concentrations in winter with significant monthly contributions to OA (18–33 %) due to enhanced residential wood burning emissions. HOA mainly originated from traffic emissions but was also influenced by biomass burning in cold periods. OOA factors were distinguished between their less- and more-oxidized fractions (LO-OOA and MO-OOA, respectively). These factors presented distinct seasonal patterns, associated with different atmospheric formation pathways. A pronounced increase of LO-OOA concentrations and contributions (50–66 %) was observed in summer, which may be mainly explained by secondary OA (SOA) formation processes involving biogenic gaseous precursors. Conversely high concentrations and OA contributions (32–62 %) of MO-OOA during winter and spring seasons were partly associated with anthropogenic emissions and/or long-range transport from northeastern Europe. The contribution of the different OA factors as a function of OA mass loading highlighted the dominant roles of POA during pollution episodes in fall and winter, and of SOA for highest springtime and summertime OA concentrations. Finally, long-term trend analyses indicated a decreasing feature (of about 200 ng m−3 yr−1) for MO-OOA, very limited or insignificant decreasing trends for primary anthropogenic carbonaceous aerosols (BBOA and HOA, along with the fossil fuel and biomass burning black carbon components), and no trend for LO-OOA over the 6+-year investigated period.


Plants ◽  
2021 ◽  
Vol 10 (2) ◽  
pp. 212
Author(s):  
Yeimi Cecilia Vega-Ruiz ◽  
Corina Hayano-Kanashiro ◽  
Nohemí Gámez-Meza ◽  
Luis Angel Medina-Juárez

Jatropha species have been shown to be an important source of secondary metabolites with different biological effects. Jatropha cinerea (Ortega) Müll. Arg and Jatropha cordata (Ortega) Müll. Arg are distributed in the Northwestern region of Mexico, are adapted to extreme weather conditions and are widely used (stems, leaves, and sap) in traditional medicine. The aim of the present study was to carry out the phytochemical characterization and the evaluation of the antioxidant activity in methanolic extracts of stems and leaves from J. cinerea and J. cordata. The compounds present in the extracts of both species were characterized by ESI-IT-MS/MS and quantified by HPLC-DAD. The results showed that the stem extracts of both species are rich in phenolic acids, while the leaf extracts are rich in flavonoids. Some of the main compounds found were gallic acid, gentisic acid, 3,4-Dihydroxybenzoic acid, vitexin, isovitexin, and catechol. Both species showed high concentrations of phenols and total flavonoids and antioxidant activity. J. cordata showed the highest antioxidant capacity and the highest concentration of phenolic compounds. Overall, both Jatropha species are a natural source of antioxidant compounds with potential biotechnological uses.


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