Mountain-valley circulation in central Chile: consequences for Black Carbon deposition over glaciers in wintertime and summertime

Author(s):  
Rémy Lapere ◽  
Sylvain Mailler ◽  
Laurent Menut ◽  
Nicolás Huneeus

<p>The configuration of the Santiago basin, Chile (33.5°S 70.65°W) is quite unique in that it combines very strong emissions of urban anthropogenic pollutants with the steep topography of the coastal and Andes cordilleras surrounding the Metropolitan area. Interactions between atmospheric pollution and mountain meteorology are therefore exacerbated, and the potential for black carbon (BC) deposition on glaciers is strong. Based on chemistry-transport modeling with WRF-CHIMERE, we investigate (i) the pathways leading to deposition of BC from Santiago up to Andean glaciers in wintertime and (ii) the differences in magnitude and time dynamics of such deposition between wintertime and summertime.</p><p>Ice and snow in the central Andes contain significant amounts of BC often attributed to emissions from Santiago. However, given the usually stable conditions in wintertime and the height of the obstacle to overcome for urban air masses (Santiago is 500 m a.s.l., summits are above 4000 m a.s.l.) the pathways for such deposition are not straightforward. We find that, for a typical winter month, up to 40% of BC dry deposition on snow- or ice-covered areas in the central Andes directly downwind from the Metropolitan area can indeed be attributed to emissions from Santiago. The adjacent network of canyons plays a key role in this export: for the case of the Maipo canyon, polluted urban air masses follow gentle slopes upward in the afternoon, consistently with mountain-valley circulation, before being vertically exported when reaching the tip of the main canyon. Statistical analysis shows that zonal wind speed in the urban area and vertical diffusion deep into the canyon account for most of the variance in BC deposition.</p><p>In summertime, more intense convection takes place, and mountain-valley circulation is seldom perturbed by cloud cover, resulting in a greater export potential. Accordingly, summertime dry deposition of BC on glaciers occurs on a regular basis with equivalent amounts each day, contrarily to a more chaotic time series in wintertime. The contribution of wet deposition in winter (nonexistent in summer) exacerbates this irregularity. However, as a consequence of weaker emissions, average monthly dry deposition of BC over the central Andes glaciers (29°S to 38°S) is found to be less than half in summertime (135 µg/m<sup>2</sup>) compared to wintertime (320 µg/m<sup>2</sup>). Given the lesser role played by wood burning for residential heating in summertime, emissions from Santiago through traffic and industry dominate the signal leading to 55% of dry deposition, while it accounts for only 14% in wintertime, at the regional scale, due to more scattered sources.</p>

2021 ◽  
Vol 13 (7) ◽  
pp. 1267
Author(s):  
Honglei Wang ◽  
Ankang Liu ◽  
Zhongxiu Zhen ◽  
Yan Yin ◽  
Bin Li ◽  
...  

As the largest independent east–west-trending mountain in the world, Mt. Tianshan exerts crucial impacts on climate and pollutant distributions in central Asia. Here, the vertical structures of meteorological elements and black carbon (BC) were first derived at Mt. Tianshan using an unmanned aerial vehicle system (UAVS). Vertical changes in meteorological elements can directly affect the structure of the planet boundary layer (PBL). As such, the influences of topography and meteorological elements’ vertical structure on aerosol distributions were explored from observations and model simulations. The mass concentrations of BC changed slightly with the increasing height below 2300 m above sea level (a.s.l.), which significantly increased with the height between 2300–3500 m a.s.l. and contrarily decreased with ascending altitude higher than 3500 m. Topography and mountain–valley winds were found to play important roles in the distributions of aerosols and BC. The prevailing valley winds in the daytime were conducive to pollutant transport from surrounding cities to Mt. Tianshan, where the aerosol number concentration and BC mass concentration increased rapidly, whereas the opposite transport pattern dominated during nighttime.


1993 ◽  
Vol 27 (7) ◽  
pp. 1327-1333 ◽  
Author(s):  
Thomas M. Holsen ◽  
Kenneth E. Noll ◽  
Guor Cheng Fang ◽  
Wen Jhy Lee ◽  
Jui Min Lin ◽  
...  

2013 ◽  
Vol 78 ◽  
pp. 259-267 ◽  
Author(s):  
Teppei J. Yasunari ◽  
Qian Tan ◽  
K.-M. Lau ◽  
Paolo Bonasoni ◽  
Angela Marinoni ◽  
...  

2014 ◽  
Vol 14 (18) ◽  
pp. 10061-10084 ◽  
Author(s):  
D. Liu ◽  
J. D. Allan ◽  
D. E. Young ◽  
H. Coe ◽  
D. Beddows ◽  
...  

Abstract. Black carbon aerosols (BC) at a London urban site were characterised in both winter- and summertime 2012 during the Clean Air for London (ClearfLo) project. Positive matrix factorisation (PMF) factors of organic aerosol mass spectra measured by a high-resolution aerosol mass spectrometer (HR-AMS) showed traffic-dominant sources in summer but in winter the influence of additional non-traffic sources became more important, mainly from solid fuel sources (SF). Measurements using a single particle soot photometer (SP2, DMT), showed the traffic-dominant BC exhibited an almost uniform BC core size (Dc) distribution with very thin coating thickness throughout the detectable range of Dc. However, the size distribution of Dc (project average mass median Dc = 149 ± 22 nm in winter, and 120 ± 6 nm in summer) and BC coating thickness varied significantly in winter. A novel methodology was developed to attribute the BC number concentrations and mass abundances from traffic (BCtr) and from SF (BCsf), by using a 2-D histogram of the particle optical properties as a function of BC core size, as measured by the SP2. The BCtr and BCsf showed distinctly different Dc distributions and coating thicknesses, with BCsf displaying larger Dc and larger coating thickness compared to BCtr. BC particles from different sources were also apportioned by applying a multiple linear regression between the total BC mass and each AMS-PMF factor (BC–AMS–PMF method), and also attributed by applying the absorption spectral dependence of carbonaceous aerosols to 7-wavelength Aethalometer measurements (Aethalometer method). Air masses that originated from westerly (W), southeasterly (SE), and easterly (E) sectors showed BCsf fractions that ranged from low to high, and whose mass median Dc values were 137 ± 10 nm, 143 ± 11 nm and 169 ± 29 nm, respectively. The corresponding bulk relative coating thickness of BC (coated particle size/BC core – Dp/Dc) for these same sectors was 1.28 ± 0.07, 1.45 ± 0.16 and 1.65 ± 0.19. For W, SE and E air masses, the number fraction of BCsf ranged from 6 ± 2% to 11 ± 5% to 18 ± 10%, respectively, but importantly the larger BC core sizes lead to an increased fraction of BCsf in terms of mass than number (for W, SE and E air masses, the BCsf mass fractions ranged from 16 ± 6%, 24 ± 10% and 39 ± 14%, respectively). An increased fraction of non-BC particles (particles that did not contain a BC core) was also observed when SF sources were more significant. The BC mass attribution by the SP2 method agreed well with the BC–AMS–PMF multiple linear regression method (BC–AMS–PMF : SP2 ratio = 1.05, r2 = 0.80) over the entire experimental period. Good agreement was found between BCsf attributed with the Aethalometer model and the SP2. However, the assumed absorption Ångström exponent (αwb) had to be changed according to the different air mass sectors to yield the best comparison with the SP2. This could be due to influences of fuel type or burn phase.


2016 ◽  
Vol 12 (5) ◽  
pp. 1165-1180 ◽  
Author(s):  
Karsten Schittek ◽  
Sebastian T. Kock ◽  
Andreas Lücke ◽  
Jonathan Hense ◽  
Christian Ohlendorf ◽  
...  

Abstract. High-altitude cushion peatlands are versatile archives for high-resolution palaeoenvironmental studies, due to their high accumulation rates, range of proxies, and sensitivity to climatic and/or human-induced changes. Especially within the Central Andes, the knowledge about climate conditions during the Holocene is limited. In this study, we present the environmental and climatic history for the last 2100 years of Cerro Tuzgle peatland (CTP), located in the dry Puna of NW Argentina, based on a multi-proxy approach. X-ray fluorescence (XRF), stable isotope and element content analyses (δ13C, δ15N, TN and TOC) were conducted to analyse the inorganic geochemistry throughout the sequence, revealing changes in the peatlands' past redox conditions. Pollen assemblages give an insight into substantial environmental changes on a regional scale. The palaeoclimate varied significantly during the last 2100 years. The results reflect prominent late Holocene climate anomalies and provide evidence that in situ moisture changes were coupled to the migration of the Intertropical Convergence Zone (ITCZ). A period of sustained dry conditions prevailed from around 150 BC to around AD 150. A more humid phase dominated between AD 200 and AD 550. Afterwards, the climate was characterised by changes between drier and wetter conditions, with droughts at around AD 650–800 and AD  1000–1100. Volcanic forcing at the beginning of the 19th century (1815 Tambora eruption) seems to have had an impact on climatic settings in the Central Andes. In the past, the peatland recovered from climatic perturbations. Today, CTP is heavily degraded by human interventions, and the peat deposit is becoming increasingly susceptible to erosion and incision.


2015 ◽  
Vol 15 (10) ◽  
pp. 5415-5428 ◽  
Author(s):  
R. Kumar ◽  
M. C. Barth ◽  
V. S. Nair ◽  
G. G. Pfister ◽  
S. Suresh Babu ◽  
...  

Abstract. This study examines differences in the surface black carbon (BC) aerosol loading between the Bay of Bengal (BoB) and the Arabian Sea (AS) and identifies dominant sources of BC in South Asia and surrounding regions during March–May 2006 (Integrated Campaign for Aerosols, Gases and Radiation Budget, ICARB) period. A total of 13 BC tracers are introduced in the Weather Research and Forecasting Model coupled with Chemistry to address these objectives. The model reproduced the temporal and spatial variability of BC distribution observed over the AS and the BoB during the ICARB ship cruise and captured spatial variability at the inland sites. In general, the model underestimates the observed BC mass concentrations. However, the model–observation discrepancy in this study is smaller compared to previous studies. Model results show that ICARB measurements were fairly well representative of the AS and the BoB during the pre-monsoon season. Elevated BC mass concentrations in the BoB are due to 5 times stronger influence of anthropogenic emissions on the BoB compared to the AS. Biomass burning in Burma also affects the BoB much more strongly than the AS. Results show that anthropogenic and biomass burning emissions, respectively, accounted for 60 and 37% of the average ± standard deviation (representing spatial and temporal variability) BC mass concentration (1341 ± 2353 ng m−3) in South Asia. BC emissions from residential (61%) and industrial (23%) sectors are the major anthropogenic sources, except in the Himalayas where vehicular emissions dominate. We find that regional-scale transport of anthropogenic emissions contributes up to 25% of BC mass concentrations in western and eastern India, suggesting that surface BC mass concentrations cannot be linked directly to the local emissions in different regions of South Asia.


2020 ◽  
Author(s):  
Sobhan Kumar Kompalli ◽  
Surendran Nair Suresh Babu ◽  
Krishnaswamy Krishnamoorthy ◽  
Sreedharan Krishnakumari Satheesh ◽  
Mukunda M. Gogoi ◽  
...  

Abstract. Regional climatic implications of aerosol black carbon (BC) are well recognized over South Asia, which has a wide variety of anthropogenic sources in a large abundance. Significant uncertainties remain in its quantification due to lack of sufficient information on the microphysical properties (its concentration, size, and mixing state with other aerosol components), which determine the absorption potential of BC. Especially the information on mixing state of BC is extremely sparse over this region. In this study, first-ever observations of the size distribution and mixing state of individual refractory black carbon (rBC) particles in the south Asian outflow to Southeastern Arabian Sea, northern and equatorial Indian Ocean regions are presented based on measurements using a single particle soot photometer (SP2) aboard the ship cruise of the Integrated Campaign for Aerosols, gases, and Radiation Budget (ICARB-2018) during winter-2018 (16 January to 13 February). The results revealed significant spatial heterogeneity of BC characteristics. Highest rBC mass concentrations (~ 938 ± 293 ng m−3) with the highest relative coating thickness (RCT; the ratio of BC core to its coating diameters) of ~ 2.16 ± 0.19 are found over the Southeast Arabian Sea (SEAS) region, which is in the proximity of the continental outflow. As we move to farther oceanic regions, though the mass concentrations decreased by nearly half (~ 546 ± 80 ng m−3), BC still remained thickly coated (RCT ~ 2.05 ± 0.07). The air over the remote equatorial Indian Ocean, which received considerable marine air masses compared to the other regions, showed the lowest rBC mass concentrations (~ 206 ± 114 ng m−3), with a moderately thick coating (RCT ~ 1.73 ± 0.16). Even over oceanic regions far from the landmass, regions which received the outflow from more industrialized east coast/the Bay of Bengal had thicker coating (~ 104 nm) compared to regions that received outflow from the west coast/peninsular India (~ 86 nm). Although different regions of the ocean depicted contrasting concentrations and mixing state parameters due to varying extent and nature of the continental outflow as well as the atmospheric lifetime of air masses, the modal parameters of rBC mass-size distributions were similar over all the regions. The observed mono-modal distribution with mean mass median diameters (MMD) in the range of 0.19–0.20 μm suggested mixed sources of BC. The mean fraction of BC containing particles (FBC) varied in the range 0.20–0.28 (suggesting significant amounts of non-BC particles), whereas the bulk mixing ratio of coating mass to rBC mass was highest (8.77 ± 2.77) over the outflow regions compared to the remote ocean (4.29 ± 1.54) highlighting the role of outflow in providing condensable material for coating on rBC. These parameters, along with the information on size-resolved mixing state of BC cores, throw light on the role of sources and secondary processing of their complex mixtures for coating on BC under highly polluted conditions. Examination of the non-refractory sub-micrometre aerosol chemical composition obtained using the aerosol chemical speciation monitor (ACSM) suggested that the overall aerosol system was sulfate dominated over the far-oceanic regions. In contrast, organics were equally prominent adjacent to the coastal landmass. Association between the BC mixing state and aerosol chemical composition suggested that sulfate was the probable dominant coating material on rBC cores.


2010 ◽  
Vol 10 (4) ◽  
pp. 9291-9328 ◽  
Author(s):  
T. J. Yasunari ◽  
P. Bonasoni ◽  
P. Laj ◽  
K. Fujita ◽  
E. Vuillermoz ◽  
...  

Abstract. The possible minimal range of reduction in snow surface albedo due to dry deposition of black carbon (BC) in the pre-monsoon period (March–May) was estimated as a lower bound together with the estimation of its accuracy, based on atmospheric observations at the Nepal Climate Observatory-Pyramid (NCO-P) sited at 5079 m a.s.l. in the Himalayan region. We estimated a total BC deposition rate of 2.89 μg m−2 day−1 providing a total deposition of 266 μg m−2 for March–May at the site, based on a calculation with a minimal deposition velocity of 1.0×10−4 m s−1 with atmospheric data of equivalent BC concentration. Main BC size at NCO-P site was determined as 103.1–669.8 nm by correlation analysis between equivalent BC concentration and particulate size distribution in the atmosphere. We also estimated BC deposition from the size distribution data and found that 8.7% of the estimated dry deposition corresponds to the estimated BC deposition from equivalent BC concentration data. If all the BC is deposited uniformly on the top 2-cm pure snow, the corresponding BC concentration is 26.0–68.2 μg kg−1 assuming snow density variations of 195–512 kg m−3 of Yala Glacier close to NCO-P site. Such a concentration of BC in snow could result in 2.0–5.2% albedo reductions. From a simple numerical calculations and if assuming these albedo reductions continue throughout the year, this would lead to a runoff increases of 70–204 mm of water drainage equivalent of 11.6–33.9% of the annual discharge of a typical Tibetan glacier. Our estimates of BC concentration in snow surface for pre-monsoon season can be considered comparable to those at similar altitude in the Himalayan region, where glaciers and perpetual snow region starts in the vicinity of NCO-P. Our estimates from only BC are likely to represent a lower bound for snow albedo reductions, since a fixed slower deposition velocity was used and atmospheric wind and turbulence effects, snow aging, dust deposition, and snow albedo feedbacks were not considered. This study represents the first investigation about BC deposition on snow from atmospheric aerosol data in Himalayas and related albedo effect is especially the first track at the southern slope of Himalayas.


2012 ◽  
Vol 64 (2) ◽  
pp. 51-62 ◽  
Author(s):  
Kazimiera Chłopek ◽  
Katarzyna Dąbrowsa-Zapart ◽  
Barbara Tokarska-Guzik

The investigation of <i>Ambrosia</i> pollen counts in the air of Sosnowiec was carried out from 1998 to 2010 by means of the volumetric method. The pollen season which was determined by means of the 98% method started at the end of July and the beginning of August and lasted until the end of October. The highest <i>Ambrosia</i> pollen count was recorded in 1999 (222 grains x m<sup>-3</sup>) and the lowest in 2001 (18 grains x m<sup>-3</sup>). It was stated that the daily count of pollen grains depended on the wind direction and maximum air temperature. The strongest correlations were found with maximum temperature and with a wind direction from the south east. A high negative correlation coefficient was found between the frequency of inflows of air masses from the west and the annual total of pollen grains and the value of the maximum daily count. The closest sites of <i>Ambrosia</i> L. are at a distance of 25-40 kilometres from the sampling point. Significant correlations with the frequency of inflow of air masses can support the conclusion that <i>Ambrosia</i> pollen grains recorded in Sosnowiec were most probably carried not only from local sources but also, at least in part, from distant places.


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