Seasonal and Elevational Variations of Black Carbon and Dust in Snow and Ice in the Solu-Khumbu, Nepal and Estimated Radiative Forcings

NASA Astrophysics Data System (ADS)

Kaspari, S.; Painter, T. H.; Gysel, M.; Skiles, M.; Schwikowski, M.

2014-12-01

Black carbon (BC) and dust deposited on snow and glacier surfaces can reduce the surface albedo, accelerate melt, and trigger albedo feedback. Assessing BC and dust concentrations in snow and ice in the Himalaya is of interest because this region borders large BC and dust sources, and seasonal snow and glacier ice in this region are an important source of water resources. Snow and ice samples were collected from crevasse profiles and snowpits at elevations between 5400 and 6400 m asl from Mera glacier located in the Solu-Khumbu region of Nepal. The samples were measured for Fe concentrations (used as a dust proxy) via ICP-MS, total impurity content gravimetrically, and BC concentrations using a Single Particle Soot Photometer (SP2). BC and Fe concentrations are substantially higher at elevations < 6000 m due to post-depositional processes including melt and sublimation and greater loading in the lower troposphere. Because the largest areal extent of snow and ice resides at elevations < 6000 m, the higher BC and dust concentrations at these elevations can reduce the snow and glacier albedo over large areas, accelerating melt, affecting glacier mass-balance and water resources, and contributing to a positive climate forcing. Radiative transfer modeling constrained by measurements at 5400 m at Mera La indicates that BC concentrations in the winter-spring snow/ice horizons are sufficient to reduce albedo by 6-10% relative to clean snow, corresponding to localized instantaneous radiative forcings of 75-120 W m-2. The other bulk impurity concentrations, when treated separately as dust, reduce albedo by 40-42% relative to clean snow and give localized instantaneous radiative forcings of 488 to 525 W m-2. Adding the BC absorption to the other impurities results in additional radiative forcings of 3 W m-2. While these results suggest that the snow albedo and radiative forcing effect of dust is considerably greater than BC, there are several sources of uncertainty.

Light-absorbing impurities accelerate glacier melt in the Central Tibetan Plateau.

PubMed

Li, Xiaofei; Kang, Shichang; He, Xiaobo; Qu, Bin; Tripathee, Lekhendra; Jing, Zhefan; Paudyal, Rukumesh; Li, Yang; Zhang, Yulan; Yan, Fangping; Li, Gang; Li, Chaoliu

2017-06-01

Light-absorbing impurities (LAIs), such as organic carbon (OC), black carbon (BC), and mineral dust (MD) deposited on the glacier surface can reduce albedo, thus accelerating the glacier melt. Surface fresh snow, aged snow, granular ice, and snowpits samples were collected between August 2014 and October 2015 on the Xiao Dongkemadi (XDKMD) glacier (33°04'N, 92°04'E) in the central Tibetan Plateau (TP). The spatiotemporal variations of LAIs concentrations in the surface snow/ice were observed to be consistent, differing mainly in magnitudes. LAIs concentrations were found to be in the order: granular ice>snowpit>aged snow>fresh snow, which must be because of post-depositional effects and enrichment. In addition, more intense melting led to higher LAIs concentrations exposed to the surface at a lower elevation, suggesting a strong negative relationship between LAIs concentrations and elevation. The scavenging efficiencies of OC and BC were same (0.07±0.02 for OC, 0.07±0.01 for BC), and the highest enrichments was observed in late September and August for surface snow and granular ice, respectively. Meanwhile, as revealed by the changes in the OC/BC ratios, intense glacier melt mainly occurred between August and October. Based on the SNow ICe Aerosol Radiative (SNICAR) model simulations, BC and MD in the surface snow/ice were responsible for about 52%±19% and 25%±14% of the albedo reduction, while the radiative forcing (RF) were estimated to be 42.74±40.96Wm -2 and 21.23±22.08Wm -2 , respectively. Meanwhile, the highest RF was observed in the granular ice, suggesting that the exposed glaciers melt and retreat more easily than the snow distributed glaciers. Furthermore, our results suggest that BC was the main forcing factor compared with MD in accelerating glacier melt during the melt season in the Central TP. Copyright © 2017 Elsevier B.V. All rights reserved.

Concentrations and Sources of Soot in Greenland Precipitation from 1788 to 2002: Implications for Radiative Forcing

NASA Astrophysics Data System (ADS)

McConnell, J. R.; Edwards, R.; Kok, G. L.; Flanner, M. G.; Zender, C. S.; Saltzman, E. S.; Banta, J. R.; Pasteris, D. R.; Carter, M. M.; Kahl, J. D.

2007-12-01

Black carbon (BC) in the atmosphere results from biomass and fossil fuel combustion. It alters chemical and physical properties of the atmosphere and snow albedo, yet little is known about BC emission or deposition histories. Monthly resolved measurements of BC in an ice core indicate that concentrations in central Greenland precipitation varied greatly during the period of record from 1788 to 2002. Parallel measurements of vanillic acid and non-sea-salt sulfur in the same ice core suggest that BC in Greenland came from wildfires and industrial activities. Prior to 1850, BC concentrations were highest in late summer to autumn and resulted primarily from boreal forest fires. Beginning about 1850, industrial emissions resulted in a seven-fold increase in ice core BC concentrations, with most change occurring in winter. BC concentrations after about 1951 were lower, probably as a result of wildfire suppression policies and the shift from coal burning to oil and gas in North America. Late 20th century increases in BC, however, may be linked to coal combustion in the rapidly expanding economies of Asia. At its maximum from 1906 to 1910, estimated surface climate forcing in early summer from BC in Arctic snow was about 3 W per square meter, more than eight times typical pre-industrial forcing.

Sources of black carbon aerosols in South Asia and surrounding regions during the Integrated Campaign for Aerosols, Gases and Radiation Budget (ICARB)

DOE PAGES

Kumar, R.; Barth, M. C.; Nair, V. S.; ...

2015-05-19

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 inlandmore » 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.« less

Top-down Estimates of Biomass Burning Emissions of Black Carbon in the Western United States

NASA Astrophysics Data System (ADS)

Mao, Y.; Li, Q.; Randerson, J. T.; Liou, K.

2011-12-01

We apply a Bayesian linear inversion to derive top-down estimates of biomass burning emissions of black carbon (BC) in the western United States (WUS) for May-November 2006 by inverting surface BC concentrations from the IMPROVE network using the GEOS-Chem chemical transport model. Model simulations are conducted at both 2°×2.5° (globally) and 0.55°×0.66° (nested over North America) horizontal resolutions. We first improve the spatial distributions and seasonal and interannual variations of the BC emissions from the Global Fire Emissions Database (GFEDv2) using MODIS 8-day active fire counts from 2005-2007. The GFEDv2 emissions in N. America are adjusted for three zones: boreal N. America, temperate N. America, and Mexico plus Central America. The resulting emissions are then used as a priori for the inversion. The a posteriori emissions are 2-5 times higher than the a priori in California and the Rockies. Model surface BC concentrations using the a posteriori estimate provide better agreement with IMPROVE observations (~20% increase in the Taylor skill score), including improved ability to capture the observed variability especially during June-July. However, model surface BC concentrations are still biased low by ~30%. Comparisons with the Fire Locating and Modeling of Burning Emissions (FLAMBE) are included.

Top-down Estimates of Biomass Burning Emissions of Black Carbon in the Western United States

NASA Astrophysics Data System (ADS)

Mao, Y.; Li, Q.; Randerson, J. T.; CHEN, D.; Zhang, L.; Liou, K.

2012-12-01

We apply a Bayesian linear inversion to derive top-down estimates of biomass burning emissions of black carbon (BC) in the western United States (WUS) for May-November 2006 by inverting surface BC concentrations from the IMPROVE network using the GEOS-Chem chemical transport model. Model simulations are conducted at both 2°×2.5° (globally) and 0.5°×0.667° (nested over North America) horizontal resolutions. We first improve the spatial distributions and seasonal and interannual variations of the BC emissions from the Global Fire Emissions Database (GFEDv2) using MODIS 8-day active fire counts from 2005-2007. The GFEDv2 emissions in N. America are adjusted for three zones: boreal N. America, temperate N. America, and Mexico plus Central America. The resulting emissions are then used as a priori for the inversion. The a posteriori emissions are 2-5 times higher than the a priori in California and the Rockies. Model surface BC concentrations using the a posteriori estimate provide better agreement with IMPROVE observations (~50% increase in the Taylor skill score), including improved ability to capture the observed variability especially during June-September. However, model surface BC concentrations are still biased low by ~30%. Comparisons with the Fire Locating and Modeling of Burning Emissions (FLAMBE) are included.

Impacts of global, regional, and sectoral black carbon emission reductions on surface air quality and human mortality

NASA Astrophysics Data System (ADS)

Anenberg, S. C.; Talgo, K.; Arunachalam, S.; Dolwick, P.; Jang, C.; West, J. J.

2011-07-01

As a component of fine particulate matter (PM2.5), black carbon (BC) is associated with premature human mortality. BC also affects climate by absorbing solar radiation and reducing planetary albedo. Several studies have examined the climate impacts of BC emissions, but the associated health impacts have been studied less extensively. Here, we examine the surface PM2.5 and premature mortality impacts of halving anthropogenic BC emissions globally and individually from eight world regions and three major economic sectors. We use a global chemical transport model, MOZART-4, to simulate PM2.5 concentrations and a health impact function to calculate premature cardiopulmonary and lung cancer deaths. We estimate that halving global anthropogenic BC emissions reduces outdoor population-weighted average PM2.5 by 542 ng m-3 (1.8 %) and avoids 157 000 (95 % confidence interval, 120 000-194 000) annual premature deaths globally, with the vast majority occurring within the source region. Most of these avoided deaths can be achieved by halving emissions in East Asia (China; 54 %), followed by South Asia (India; 31 %), however South Asian emissions have 50 % greater mortality impacts per unit BC emitted than East Asian emissions. Globally, halving residential, industrial, and transportation emissions contributes 47 %, 35 %, and 15 % to the avoided deaths from halving all anthropogenic BC emissions. These contributions are 1.2, 1.2, and 0.6 times each sector's portion of global BC emissions, owing to the degree of co-location with population globally. We find that reducing BC emissions increases regional SO4 concentrations by up to 28 % of the magnitude of the regional BC concentration reductions, due to reduced absorption of radiation that drives photochemistry. Impacts of residential BC emissions are likely underestimated since indoor PM2.5 exposure is excluded. We estimate ∼8 times more avoided deaths when BC and organic carbon (OC) emissions are halved together, suggesting that these results greatly underestimate the full air pollution-related mortality benefits of BC mitigation strategies which generally decrease both BC and OC. The choice of concentration-response factor and health effect thresholds affects estimated global avoided deaths by as much as 56 % but does not strongly affect the regional distribution. Confidence in our results would be strengthened by reducing uncertainties in emissions, model parameterization of aerosol processes, grid resolution, and PM2.5 concentration-mortality relationships globally.

Flux, Budget and Sources of Black Carbon (BC) in the Continental Shelf of the Bohai and Yellow Seas, China

NASA Astrophysics Data System (ADS)

Fang, Y.; Chen, Y.; Tian, C.

2015-12-01

Black carbon (BC) derived from incomplete combustion of fossil fuels and biomass has received increasing attention due to their potential importance in a wide range of biogeochemical processes. China has been generally considered as the world's largest BC emitter. Due to a combination of the prevailing East Asia monsoon and large amounts of riverine outflow, BC released from China can be transported to the adjacent continental shelf seas, the Bohai Sea (BS) and Yellow Sea (YS). Based on measurements of BC in 191 surface sediments, 36 riverine water, and 2 seawater samples, as well as the reported BC data set of the aerosol samples in the Bohai Rim, the concentration, flux, and budget of BC in the BS and YS were investigated. The spatial distribution of the BC concentration in surface sediments was largely influenced by the regional hydrodynamic conditions, with high values mainly occurring in the central mud areas. The BC burial flux in the BS and YS ranged from 4 to 1100 μg/cm2/yr, and averaged 166 ± 200 μg/cm2/yr. The area-integrated sedimentary BC sink flux in the entire BS and YS was ~325 Gg/yr. The BC budget calculated in the BS showed that atmospheric deposition and riverine discharge played comparable importance in delivering BC to the BS, and sequestration to bottom sediments was the major BC output pattern, accounting for ~88% of the total input BC. Besides, we attempted to apportion the BC sources in the BS and YS surface sediments using PAHs (organic molecular proxies cogenerated with BC) and BC as an input data to the Positive Matrix Factorization (PMF) receptor model. Results showed that ~83% of the sediment BC was attributed to the combustion of fossil fuels, and the remaining ~17% was from biomass burning. Due to the differences in their production mechanisms and therefore physicochemical properties, the above distinction and quantification would help us better understand their different environmental behaviors in the complex continental shelf regimes.

Enhanced light absorptivity of black carbon with air pollution development in urban Beijing, China

NASA Astrophysics Data System (ADS)

Zhang, Y.; Zhang, Q.; Cheng, Y.; Su, H.; He, K.

2017-12-01

The impacts of black carbon (BC) aerosols on air quality and climate are dependent on BC light absorptivity. However, the light absorptivity of ambient BC-containing particles remains conflicting. In this work, we investigated the evolution of BC light absorptivity with pollution development in urban Beijing, China. We found that the mass absorption cross-section (MAC) of ambient BC-containing particles measured during the campaign increased with BC mass concentration, which can be attributed to more coating materials on BC surface with pollution development. A single-particle soot photometer (SP2) measurement showed that the coating thickness (CT) of BC-containing particles increased by 48% with PM1 and BC mass concentration increasing from 10 μg m-3 and 0.3 μg m-3 to 230 μg m-3 and 12 μg m-3. Based on Mie calculation, the CT increase could led to light absorption enhancement (Eab) of BC-containing particles increasing by 22%, consistent with the increase of measured MAC. The relationship between growth rate of BC light absorptivity (kEab) and that of PM1 or rBC concentration (kPM1 or krBC) showed that kEab ≈ 4.8% kPM1 or kEab ≈ 2.5% krBC. The analysis of effective emission intensity (EEI) for BC revealed that the enhancement of BC light absorptivity with increasing pollution levels was dominated by regional transport. During the pollution period, 63% of BC over Beijing originated from regional sources. The aging of these regional BC during atmospheric transport controlled the increase of coating materials for BC-containing particles observed in Beijing. As a result of enhanced light absorptivity with pollution development, BC forcing efficiency could increase by 20% during polluted period. Our work identified the importance of BC on radiative forcing under polluted environment, which is determined by not only the increase of BC mass concentration, but also the enhancement of BC forcing efficiency due to more coating materials.

Preliminary Estimation of Black Carbon Deposition from Nepal Climate Observatory-Pyramid Data and Its Possible Impact on Snow Albedo Changes Over Himalayan Glaciers During the Pre-Monsoon Season

NASA Technical Reports Server (NTRS)

Yasunari, T. J.; Bonasoni, P.; Laj, P.; Fujita, K.; Vuillermoz, E.; Marinoni, A.; Cristofanelli, P.; Duchi, R.; Tartari, G.; Lau, K.-M.

2010-01-01

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 g m-2 day-1 providing a total deposition of 266 micrograms/ square m for March-May at the site, based on a calculation with a minimal deposition velocity of 1.0 10(exp -4) m/s 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 microgram/kg assuming snow density variations of 195-512 kg/ cubic m 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.

Major fraction of black carbon is flushed from the melting New Hampshire snowpack nearly as quickly as soluble impurities

NASA Astrophysics Data System (ADS)

Lazarcik, James; Dibb, Jack E.; Adolph, Alden C.; Amante, Jacqueline M.; Wake, Cameron P.; Scheuer, Eric; Mineau, Madeleine M.; Albert, Mary R.

2017-01-01

Seasonal snowpacks accumulate impurities derived from atmospheric aerosols and trace gases throughout the winter and release them during snowmelt. Previous field and laboratory studies have shown that a snowpack can lose up to 80% of the soluble ion burden in the first 20% of the melt, an event commonly known as an ionic pulse. Other studies have concluded that particulate impurities (e.g., black carbon (BC)) concentrate in surface layers during melt which can have important implications for snowpack albedo. However, model and field studies have indicated that meltwater scavenging efficiency of BC in melting snowpacks is still an area of uncertainty. To quantify BC melt dynamics and the release of soluble impurities, we collected and analyzed near-daily chemical profiles in the snowpack at three sites during two winters in New Hampshire, United States of America. We observe an ionic pulse and a pulse of BC from the snowpack at the onset of melt; up to 62% of BC leaves within the first 24% of the melt. Surface concentrations of BC are higher than seasonal medians at the end of the winter season, but surface enhancements do not appear to be closely linked to decreases in snow-water equivalence caused by melting.

The Spectral and Chemical Measurement of Pollutants on Snow Near South Pole, Antarctica

NASA Technical Reports Server (NTRS)

Casey, K. A.; Kaspari, S. D.; Skiles, S. M.; Kreutz, K.; Handley, M. J.

2017-01-01

Remote sensing of light-absorbing particles (LAPs), or dark colored impurities, such as black carbon (BC) and dust on snow, is a key remaining challenge in cryospheric surface characterization and application to snow, ice, and climate models. We present a quantitative data set of in situ snow reflectance, measured and modeled albedo, and BC and trace element concentrations from clean to heavily fossil fuel emission contaminated snow near South Pole, Antarctica. Over 380 snow reflectance spectra (350-2500 nm) and 28 surface snow samples were collected at seven distinct sites in the austral summer season of 2014-2015. Snow samples were analyzed for BC concentration via a single particle soot photometer and for trace element concentration via an inductively coupled plasma mass spectrometer. Snow impurity concentrations ranged from 0.14 to 7000 part per billion (ppb) BC, 9.5 to 1200 ppb sulfur, 0.19 to 660 ppb iron, 0.013 to 1.9 ppb chromium, 0.13 to 120 ppb copper, 0.63 to 6.3 ppb zinc, 0.45 to 82 parts per trillion (ppt) arsenic, 0.0028 to 6.1 ppb cadmium, 0.062 to 22 ppb barium, and 0.0044 to 6.2 ppb lead. Broadband visible to shortwave infrared albedo ranged from 0.85 in pristine snow to 0.62 in contaminated snow. LAP radiative forcing, the enhanced surface absorption due to BC and trace elements, spanned from less than 1 W m(exp. -2) for clean snow to approximately 70 W m(exp. -2) for snow with high BC and trace element content. Measured snow reflectance differed from modeled snow albedo due to specific impurity-dependent absorption features, which we recommend be further studied and improved in snow albedo models.

The spectral and chemical measurement of pollutants on snow near South Pole, Antarctica

NASA Astrophysics Data System (ADS)

Casey, K. A.; Kaspari, S. D.; Skiles, S. M.; Kreutz, K.; Handley, M. J.

2017-06-01

Remote sensing of light-absorbing particles (LAPs), or dark colored impurities, such as black carbon (BC) and dust on snow, is a key remaining challenge in cryospheric surface characterization and application to snow, ice, and climate models. We present a quantitative data set of in situ snow reflectance, measured and modeled albedo, and BC and trace element concentrations from clean to heavily fossil fuel emission contaminated snow near South Pole, Antarctica. Over 380 snow reflectance spectra (350-2500 nm) and 28 surface snow samples were collected at seven distinct sites in the austral summer season of 2014-2015. Snow samples were analyzed for BC concentration via a single particle soot photometer and for trace element concentration via an inductively coupled plasma mass spectrometer. Snow impurity concentrations ranged from 0.14 to 7000 part per billion (ppb) BC, 9.5 to 1200 ppb sulfur, 0.19 to 660 ppb iron, 0.013 to 1.9 ppb chromium, 0.13 to 120 ppb copper, 0.63 to 6.3 ppb zinc, 0.45 to 82 parts per trillion (ppt) arsenic, 0.0028 to 6.1 ppb cadmium, 0.062 to 22 ppb barium, and 0.0044 to 6.2 ppb lead. Broadband visible to shortwave infrared albedo ranged from 0.85 in pristine snow to 0.62 in contaminated snow. LAP radiative forcing, the enhanced surface absorption due to BC and trace elements, spanned from <1 W m-2 for clean snow to 70 W m-2 for snow with high BC and trace element content. Measured snow reflectance differed from modeled snow albedo due to specific impurity-dependent absorption features, which we recommend be further studied and improved in snow albedo models.

Light-absorbing Aerosol Properties in the Kathmandu Valley during SusKat-ABC Field Campaign

NASA Astrophysics Data System (ADS)

Kim, S.; Yoon, S.; Kim, J.; Cho, C.; Jung, J.

2013-12-01

Light-absorbing aerosols, such as black carbon (BC), are major contributors to the atmospheric heating and the reduction of solar radiation reaching at the earth's surface. In this study, we investigate light-absorption and scattering properties of aerosols (i.e., BC mass concentration, aerosol solar-absorption/scattering efficiency) in the Kathmandu valley during Sustainable atmosphere for the Kathmandu valley (SusKat)-ABC campaign, from December 2012 to February 2013. Kathmandu City is among the most polluted cities in the world. However, there are only few past studies that provide basic understanding of air pollution in the Kathmandu Valley, which is not sufficient for designing effective mitigation measures (e.g., technological, financial, regulatory, legal and political measures, planning strategies). A distinct diurnal variation of BC mass concentration with two high peaks observed during wintertime dry monsoon period. BC mass concentration was found to be maximum around 09:00 and 20:00 local standard time (LST). Increased cars and cooking activities including substantial burning of wood and other biomass in the morning and in the evening contributed to high BC concentration. Low BC concentrations during the daytime can be explain by reduced vehicular movement and cooking activities. Also, the developmements of the boundary layer height and mountain-valley winds in the Kathmandu Valley paly a crucial role in the temproal variation of BC mass concentrations. Detailed radiative effects of light-absorbing aerosols will be presented.

Temporal variation and source identification of black carbon at Lin'an and Longfengshan regional background stations in China

NASA Astrophysics Data System (ADS)

Cheng, Siyang; Wang, Yaqiang; An, Xingqin

2017-12-01

Black carbon (BC) is a component of fine particulate matter (PM2.5), associated with climate, weather, air quality, and people's health. However, studies on temporal variation of atmospheric BC concentration at background stations in China and its source area identification are lacking. In this paper, we use 2-yr BC observations from two background stations, Lin'an (LAN) and Longfengshan (LFS), to perform the investigation. The results show that the mean diurnal variation of BC has two significant peaks at LAN while different characteristics are found in the BC variation at LFS, which are probably caused by the difference in emission source contributions. Seasonal variation of monthly BC shows double peaks at LAN but a single peak at LFS. The annual mean concentrations of BC at LAN and LFS decrease by 1.63 and 0.26 μg m-3 from 2009 to 2010, respectively. The annual background concentration of BC at LAN is twice higher than that at LFS. The major source of the LAN BC is industrial emission while the source of the LFS BC is residential emission. Based on transport climatology on a 7-day timescale, LAN and LFS stations are sensitive to surface emissions respectively in belt or approximately circular area, which are dominated by summer monsoon or colder land air flows in Northwest China. In addition, we statistically analyze the BC source regions by using BC observation and FLEXible PARTicle dispersion model (FLEXPART) simulation. In summer, the source regions of BC are distributed in the northwest and south of LAN and the southwest of LFS. Low BC concentration is closely related to air mass from the sea. In winter, the source regions of BC are concentrated in the west and south of LAN and the northeast of the threshold area of s tot at LFS. The cold air mass in the northwest plays an important role in the purification of atmospheric BC. On a yearly scale, sources of BC are approximately from five provinces in the northwest/southeast of LAN and the west of LFS. These findings are helpful in reducing BC emission and controlling air pollution.

Radiative effect of black carbon aerosol on a squall line case in North China

NASA Astrophysics Data System (ADS)

Fu, Shizuo; Deng, Xin; Li, Zhe; Xue, Huiwen

2017-11-01

The radiative effect of black carbon aerosol (BC) on a squall line case in north China is studied with the Weather Research and Forecasting model. Before the initiation of the squall line, the surface-emitted BC is mixed only in the boundary layer (BL). BC is then transported from the BL into the free troposphere by the updrafts in the squall line system. Once distributed in the atmosphere, BC absorbs solar radiation and heats the surrounding air. The maximum increase of temperature is 0.05 K for the moderately polluted case bc2 and 0.37 K for the heavily polluted case bc20. In case bc2, where the BC concentration is not very high, the solar flux reaching the surface, the sensible heat flux, and the latent heat flux are not significantly affected by BC. In case bc20, the solar flux reaching the surface, the sensible heat flux, and the latent heat flux are reduced by up to 80, 30, and 21 W m- 2, respectively. The reduced surface evaporation leads to a reduced vapor amount at the early stage. After some time, the heating effect causes a large-scale convergence and brings slightly more vapor into the domain. The effect of BC on the cold pool strength and low-level wind shear is small and hence does not significantly affect the triggering of new convections. In addition, our results show that the effect of BC is negligible on the strength and rain rate of the squall line case.

Light-absorbing impurities in a southern Tibetan Plateau glacier: Variations and potential impact on snow albedo and radiative forcing

NASA Astrophysics Data System (ADS)

Li, Xiaofei; Kang, Shichang; Zhang, Guoshuai; Qu, Bin; Tripathee, Lekhendra; Paudyal, Rukumesh; Jing, Zhefan; Zhang, Yulan; Yan, Fangping; Li, Gang; Cui, Xiaoqing; Xu, Rui; Hu, Zhaofu; Li, Chaoliu

2018-02-01

Light-absorbing impurities (LAIs), such as organic carbon (OC), black carbon (BC), and mineral dust (MD), deposited on the surface snow of glacier can reduce the surface albedo. As there exists insufficient knowledge to completely characterize LAIs variations and difference in LAIs distributions, it is essential to investigate the behaviors of LAIs and their influence on the glaciers across the Tibetan Plateau (TP). Therefore, surface snow and snowpit samples were collected during September 2014 to September 2015 from Zhadang (ZD) glacier in the southern TP to investigate the role of LAIs in the glacier. LAIs concentrations were observed to be higher in surface aged snow than in the fresh snow possibly due to post-depositional processes such as melting or sublimation. The LAIs concentrations showed a significant spatial distribution and marked negative relationship with elevation. Impurity concentrations varied significantly with depth in the vertical profile of the snowpit, with maximum LAIs concentrations frequently occurred in the distinct dust layers which were deposited in non-monsoon, and the bottom of snowpit due to the eluviation in monsoon. Major ions in snowpit and backward trajectory analysis indicated that regional activities and South Asian emissions were the major sources. According to the SNow ICe Aerosol Radiative (SNICAR) model, the average simulated albedo caused by MD and BC in aged snow collected on 31 May 2015 accounts for about 13% ± 3% and 46% ± 2% of the albedo reduction. Furthermore, we also found that instantaneous RF caused by MD and BC in aged snow collected on 31 May 2015 varied between 4-16 W m- 2 and 7-64 W m- 2, respectively. The effect of BC exceeds that of MD on albedo reduction and instantaneous RF in the study area, indicating that BC played a major role on the surface of the ZD glacier.

Tethered balloon-born and ground-based measurements of black carbon and particulate profiles within the lower troposphere during the foggy period in Delhi, India.

PubMed

Bisht, D S; Tiwari, S; Dumka, U C; Srivastava, A K; Safai, P D; Ghude, S D; Chate, D M; Rao, P S P; Ali, K; Prabhakaran, T; Panickar, A S; Soni, V K; Attri, S D; Tunved, P; Chakrabarty, R K; Hopke, P K

2016-12-15

The ground and vertical profiles of particulate matter (PM) were mapped as part of a pilot study using a Tethered balloon within the lower troposphere (1000m) during the foggy episodes in the winter season of 2015-16 in New Delhi, India. Measurements of black carbon (BC) aerosol and PM <2.5 and 10μm (PM 2.5 & PM 10 respectively) concentrations and their associated particulate optical properties along with meteorological parameters were made. The mean concentrations of PM 2.5 , PM 10 , BC 370 nm, and BC 880 nm were observed to be 146.8±42.1, 245.4±65.4, 30.3±12.2, and 24.1±10.3μgm -3 , respectively. The mean value of PM 2.5 was ~12 times higher than the annual US-EPA air quality standard. The fraction of BC in PM 2.5 that contributed to absorption in the shorter visible wavelengths (BC 370 nm ) was ~21%. Compared to clear days, the ground level mass concentrations of PM 2.5 and BC 370 nm particles were substantially increased (59% and 24%, respectively) during the foggy episode. The aerosol light extinction coefficient (σ ext ) value was much higher (mean: 610Mm -1 ) during the lower visibility (foggy) condition. Higher concentrations of PM 2.5 (89μgm -3 ) and longer visible wavelength absorbing BC 880 nm (25.7μgm -3 ) particles were observed up to 200m. The BC 880 nm and PM 2.5 aerosol concentrations near boundary layer (1km) were significantly higher (~1.9 and 12μgm -3 ), respectively. The BC (i.e BC tot ) aerosol direct radiative forcing (DRF) values were estimated at the top of the atmosphere (TOA), surface (SFC), and atmosphere (ATM) and its resultant forcing were - 75.5Wm -2 at SFC indicating the cooling effect at the surface. A positive value (20.9Wm -2 ) of BC aerosol DRF at TOA indicated the warming effect at the top of the atmosphere over the study region. The net DRF value due to BC aerosol was positive (96.4Wm -2 ) indicating a net warming effect in the atmosphere. The contribution of fossil and biomass fuels to the observed BC aerosol DRF values was ~78% and ~22%, respectively. The higher mean atmospheric heating rate (2.71Kday -1 ) by BC aerosol in the winter season would probably strengthen the temperature inversion leading to poor dispersion and affecting the formation of clouds. Serious detrimental impacts on regional climate due to the high concentrations of BC and PM (especially PM 2.5 ) aerosol are likely based on this study and suggest the need for immediate, stringent measures to improve the regional air quality in the northern India. Copyright © 2016 Elsevier B.V. All rights reserved.

Sensitivity of black carbon concentrations and climate impact to aging and scavenging in OsloCTM2-M7

NASA Astrophysics Data System (ADS)

Lund, Marianne T.; Berntsen, Terje K.; Samset, Bjørn H.

2017-05-01

Accurate representation of black carbon (BC) concentrations in climate models is a key prerequisite for understanding its net climate impact. BC aging and scavenging are treated very differently in current models. Here, we examine the sensitivity of three-dimensional (3-D), temporally resolved BC concentrations to perturbations to individual model processes in the chemistry transport model OsloCTM2-M7. The main goals are to identify processes related to aerosol aging and scavenging where additional observational constraints may most effectively improve model performance, in particular for BC vertical profiles, and to give an indication of how model uncertainties in the BC life cycle propagate into uncertainties in climate impacts. Coupling OsloCTM2 with the microphysical aerosol module M7 allows us to investigate aging processes in more detail than possible with a simpler bulk parameterization. Here we include, for the first time in this model, a treatment of condensation of nitric acid on BC. Using kernels, we also estimate the range of radiative forcing and global surface temperature responses that may result from perturbations to key tunable parameters in the model. We find that BC concentrations in OsloCTM2-M7 are particularly sensitive to convective scavenging and the inclusion of condensation by nitric acid. The largest changes are found at higher altitudes around the Equator and at low altitudes over the Arctic. Convective scavenging of hydrophobic BC, and the amount of sulfate required for BC aging, are found to be key parameters, potentially reducing bias against HIAPER Pole-to-Pole Observations (HIPPO) flight-based measurements by 60 to 90 %. Even for extensive tuning, however, the total impact on global-mean surface temperature is estimated to less than 0.04 K. Similar results are found when nitric acid is allowed to condense on the BC aerosols. We conclude, in line with previous studies, that a shorter atmospheric BC lifetime broadly improves the comparison with measurements over the Pacific. However, we also find that the model-measurement discrepancies can not be uniquely attributed to uncertainties in a single process or parameter. Model development therefore needs to be focused on improvements to individual processes, supported by a broad range of observational and experimental data, rather than tuning of individual, effective parameters such as the global BC lifetime.

Measurements of Refractory Black Carbon (rBC) Aerosols in the McMurdo Dry Valleys, Antarctica

NASA Astrophysics Data System (ADS)

Khan, A. L.; McMeeking, G. R.; Lyons, W. B.; Schwarz, J. P.; Welch, K. A.; McKnight, D. M.

2015-12-01

Measurements of light absorbing particles in the boundary layer of the high southern latitudes are scarce. During the 2013-2014 austral summer field season refractory black carbon (rBC) aerosols were quantified by a single particle soot photometer (SP2) in the McMurdo Dry Valleys, Antarctica. The dark rBC particles absorb more radiation thereby increasing atmospheric heating, as well as reducing surface albedo and enhancing hydrologic melt when deposited on highly reflective surfaces such as snow and ice. Quantifying both local and long-range atmospheric transport of rBC to this region of a remote continent mostly covered by ice and snow would be useful in understanding meltwater generation as climate changes. Although the Dry Valleys are the largest ice-free region of Antarctica, they contain many alpine glaciers, some of which are fed from the East Antarctic Ice Sheet (EAIS). Continuous rBC measurements were collected at Lake Hoare Camp in the Taylor Valley for two months, along with shorter periods at more remote locations within the Dry Valleys. Conditions at the Lake Hoare Camp were dominated by up-valley winds from McMurdo Sound, however, winds also brought air down-valley from the EAIS polar plateau. Here we investigated periods dominated by both up and down-valley winds to explore differences in rBC concentrations, size distributions, and scattering properties. The average background rBC mass concentration was 1ng/m3, though concentrations as high as 50 ng/m3 were observed at times, likely due to local sources.

Changes in Fire-Derived Soil Black Carbon Storage in a Sub-humid Woodland

NASA Astrophysics Data System (ADS)

White, J. D.; Yao, J.; Murray, D. B.; Hockaday, W. C.

2014-12-01

Fire-derived black carbon (BC) in soil, including charcoal, represents a potentially important fraction of terrestrial carbon cycling due to its presumed long persistence in soil. Interpretation of site BC retention is important for assessing feedbacks to ecosystem processes including nutrient and water cycling. However, interaction between vegetation disturbance, BC formation, and off site transport may exist that complicate interpretation of BC addition to soils from wildfire or prescribed burns directly. To investigate the relationship between disturbance and site retention on soil BC, we determined BC concentrations for a woodland in central Texas, USA, from study plots in hilly terrain with a fire scar dendrochronology spanning 100 years. BC values were determined from 13C nuclear magnetic resonance (NMR) spectroscopy. Estimated values showed mean BC concentration of 2.73 ± 3.06 g BC kg-1 (0.91 ± 0.51 kg BC m-2) for sites with fire occurrence within the last 40 years compared with BC values of1.21 ± 1.70 g BC kg-1 soil (0.18 ± 0.14 kg BC m-2) for sites with fire 40 - 100 years ago. Sites with no tree ring evidence of fire during the last 100 years had the lowest mean soil BC concentration of 0.05 ± 0.11 g BC kg-1 (0.02 ± 0.03 kg BC m-2). Molecular proxies of stability (lignin/N) and decomposition (Alkyl C/O-Alky C) showed no differences across the sites, indicating that low potential for BC mineralization. Modeled soil erosion and time since fire from fire scar data showed that soil BC concentrations were inversely correlated. A modified the ecosystem process model, Biome-BGC, was also used simulate the effects of fire disturbance with different severities and seasonality on C cycling related to the BC production, effect on soil water availability, and off-site transport. Results showed that BC impacts on ecosystem processes, including net ecosystem exchange and leaf area development, were predominantly related to fire frequency. Site BC loss rates were affected by initial slope-affected erosion, fire severity, vegetation type, and rate of vegetation recovery. The simulation results showed that fire types, such as high severity, was generally associated with low site BC retention related to low vertical transfer of BC into soils, buoyancy of BC particles, and surface runoff from unvegetated soils.

Confronting the “Indian summer monsoon response to black carbon aerosol” with the uncertainty in its radiative forcing and beyond

DOE PAGES

Kovilakam, Mahesh; Mahajan, Salil

2016-06-28

While black carbon aerosols (BC) are believed to modulate the Indian monsoons, the radiative forcing estimate of BC suffers from large uncertainties globally. In this paper, we analyze a suite of idealized experiments forced with a range of BC concentrations that span a large swath of the latest estimates of its global radiative forcing. Within those bounds of uncertainty, summer precipitation over the Indian region increases nearly linearly with the increase in BC burden. The linearity holds even as the BC concentration is increased to levels resembling those hypothesized in nuclear winter scenarios, despite large surface cooling over India andmore » adjoining regions. The enhanced monsoonal circulation is associated with a linear increase in the large-scale meridional tropospheric temperature gradient. The precipitable water over the region also increases linearly with an increase in BC burden, due to increased moisture transport from the Arabian sea to the land areas. The wide range of Indian monsoon response elicited in these experiments emphasizes the need to reduce the uncertainty in BC estimates to accurately quantify their role in modulating the Indian monsoons. Finally, the increase in monsoonal circulation in response to large BC concentrations contrasts earlier findings that the Indian summer monsoon may break down following a nuclear war.« less

Confronting the “Indian summer monsoon response to black carbon aerosol” with the uncertainty in its radiative forcing and beyond

DOE Office of Scientific and Technical Information (OSTI.GOV)

Kovilakam, Mahesh; Mahajan, Salil

While black carbon aerosols (BC) are believed to modulate the Indian monsoons, the radiative forcing estimate of BC suffers from large uncertainties globally. In this paper, we analyze a suite of idealized experiments forced with a range of BC concentrations that span a large swath of the latest estimates of its global radiative forcing. Within those bounds of uncertainty, summer precipitation over the Indian region increases nearly linearly with the increase in BC burden. The linearity holds even as the BC concentration is increased to levels resembling those hypothesized in nuclear winter scenarios, despite large surface cooling over India andmore » adjoining regions. The enhanced monsoonal circulation is associated with a linear increase in the large-scale meridional tropospheric temperature gradient. The precipitable water over the region also increases linearly with an increase in BC burden, due to increased moisture transport from the Arabian sea to the land areas. The wide range of Indian monsoon response elicited in these experiments emphasizes the need to reduce the uncertainty in BC estimates to accurately quantify their role in modulating the Indian monsoons. Finally, the increase in monsoonal circulation in response to large BC concentrations contrasts earlier findings that the Indian summer monsoon may break down following a nuclear war.« less

Dependency of black-carbon-induced atmospheric warming on the concentration of sulphate and organic aerosols

NASA Astrophysics Data System (ADS)

Kim, S.; Yoon, S.; in-Jin, C.; Ramanathan, V.; Ramana, M.

2010-12-01

Previous modeling studies have showed that the net radiative effect of black carbon (BC) and organic aerosols generated by fossil-fuel combustion and biomass-fuel cooking contribute to a warming by absorbing solar radiation, and the warming effect of fossil-fuel BC is larger than that of biomass-fuel cooking [Ramana et al., Nature Geoscience, 2010]. However, the extent of BC warming is regulated by the ambient concentrations of sulphate and organic carbon (OC) aerosols, which reflect the solar radiation and cool the surface, thus enhancing the net warming caused by BC and GHGs. This is because the major sources of BC also emit CO2 and other greenhouse gases (GHGs) (that warm the climate), and sulfates, nitrates, organics and other particles (that cool the climate). In this study, we present the impact of BC-to-sulphate and BC-to-OC ratios on atmospheric warming on the basis of surface-based filter and in-situ measurements at Gosan climate observatory in Jeju, South Korea and radiative transfer calculations with AERONET Cimel sun/sky radiometer and micro-pulse lidar measurements as a model input. We investigate (1) BC-to-sulphate and BC-to-OC ratios, (2) aerosol solar-absorption efficiency (i.e., co-single scattering albedo) and (3) corresponding atmospheric direct radiative forcing and heating rate of aerosol plumes from N. China (Beijing), S. China (Shanghai) and clean marine sources during ACE-Asia (April-May 2001), ABC-EAREX2005 (March-April 2005) and CAMPEX (August-September 2008), and discuss their relationships.

Source attribution of black carbon and its direct radiative forcing in China

DOE Office of Scientific and Technical Information (OSTI.GOV)

Yang, Yang; Wang, Hailong; Smith, Steven J.

The source attributions for mass concentration, haze formation, transport and direct radiative forcing of black carbon (BC) in various regions of China are quantified in this study using the Community Earth System Model (CESM) with a source-tagging technique. Anthropogenic emissions are from the Community Emissions Data System that is newly developed for the Coupled Model Intercomparison Project Phase 6 (CMIP6). Over north China where the air quality is often poor, about 90 % of near-surface BC concentration is contributed by local emissions. Overall, 35 % of BC concentration over south China in winter can be attributed to emissions from north China, andmore » 19 % comes from sources outside China in spring. For other regions in China, BC is largely contributed from nonlocal sources. We further investigated potential factors that contribute to the poor air quality in China. During polluted days, a net inflow of BC transported from nonlocal source regions associated with anomalous winds plays an important role in increasing local BC concentrations. BC-containing particles emitted from East Asia can also be transported across the Pacific. Our model results show that emissions from inside and outside China are equally important for the BC outflow from East Asia, while emissions from China account for 8 % of BC concentration and 29 % in column burden in the western United States in spring. Radiative forcing estimates show that 65 % of the annual mean BC direct radiative forcing (2.2 W m −2) in China results from local emissions, and the remaining 35 % is contributed by emissions outside of China. Efficiency analysis shows that a reduction in BC emissions over eastern China could have a greater benefit for the regional air quality in China, especially in the winter haze season.« less

Source attribution of black carbon and its direct radiative forcing in China

DOE PAGES

Yang, Yang; Wang, Hailong; Smith, Steven J.; ...

2017-03-30

The source attributions for mass concentration, haze formation, transport and direct radiative forcing of black carbon (BC) in various regions of China are quantified in this study using the Community Earth System Model (CESM) with a source-tagging technique. Anthropogenic emissions are from the Community Emissions Data System that is newly developed for the Coupled Model Intercomparison Project Phase 6 (CMIP6). Over north China where the air quality is often poor, about 90 % of near-surface BC concentration is contributed by local emissions. Overall, 35 % of BC concentration over south China in winter can be attributed to emissions from north China, andmore » 19 % comes from sources outside China in spring. For other regions in China, BC is largely contributed from nonlocal sources. We further investigated potential factors that contribute to the poor air quality in China. During polluted days, a net inflow of BC transported from nonlocal source regions associated with anomalous winds plays an important role in increasing local BC concentrations. BC-containing particles emitted from East Asia can also be transported across the Pacific. Our model results show that emissions from inside and outside China are equally important for the BC outflow from East Asia, while emissions from China account for 8 % of BC concentration and 29 % in column burden in the western United States in spring. Radiative forcing estimates show that 65 % of the annual mean BC direct radiative forcing (2.2 W m −2) in China results from local emissions, and the remaining 35 % is contributed by emissions outside of China. Efficiency analysis shows that a reduction in BC emissions over eastern China could have a greater benefit for the regional air quality in China, especially in the winter haze season.« less

Emission inventories for ships in the arctic based on satellite sampled AIS data

NASA Astrophysics Data System (ADS)

Winther, Morten; Christensen, Jesper H.; Plejdrup, Marlene S.; Ravn, Erik S.; Eriksson, Ómar F.; Kristensen, Hans Otto

2014-07-01

This paper presents a detailed BC, NOx and SO2 emission inventory for ships in the Arctic in 2012 based on satellite AIS data, ship engine power functions and technology stratified emission factors. Emission projections are presented for the years 2020, 2030 and 2050. Furthermore, the BC, SO2 and O3 concentrations and the deposition of BC are calculated for 2012 and for two arctic shipping scenarios - with or without arctic diversion routes due to a possible polar sea ice extent in the future. In 2012, the largest shares of Arctic ships emissions are calculated for fishing ships (45% for BC, 38% for NOx, 23% for SO2) followed by passenger ships (20%, 17%, 25%), tankers (9%, 13%, 15%), general cargo (8%, 11%, 12%) and container ships (5%, 7%, 8%). In 2050, without arctic diversion routes, the total emissions of BC, NOx and SO2 are expected to change by +16%, -32% and -63%, respectively, compared to 2012. The results for fishing ships are the least certain, caused by a less precise engine power - sailing speed relation. The calculated BC, SO2, and O3 surface concentrations and BC deposition contributions from ships are low as a mean for the whole Arctic in 2012, but locally BC additional contributions reach up to 20% around Iceland, and high additional contributions (100-300%) are calculated in some sea areas for SO2. In 2050, the arctic diversion routes highly influence the calculated surface concentrations and the deposition of BC in the Arctic. During summertime navigation contributions become very visible for BC (>80%) and SO2 (>1000%) along the arctic diversion routes, while the O3 (>10%) and BC deposition (>5%) additional contributions, respectively, get highest over the ocean east of Greenland and in the High Arctic. The geospatial ship type specific emission results presented in this paper have increased the accuracy of the emission inventories for ships in the Arctic. The methodology can be used to estimate shipping emissions in other regions of the world, and hence may serve as an input for other researchers and policy makers working in this field.

Biochar composites with nano zerovalent iron and eggshell powder for nitrate removal from aqueous solution with coexisting chloride ions.

PubMed

Ahmad, Munir; Ahmad, Mahtab; Usman, Adel R A; Al-Faraj, Abdullah S; Abduljabbar, Adel S; Al-Wabel, Mohammad I

2017-09-18

Biochar (BC) was produced from date palm tree leaves and its composites were prepared with nano zerovalent iron (nZVI-BC) and hen eggshell powder (EP-BC). The produced BC and its composites were characterized by SEM, XRD, BET, and FTIR for surface structural, mineralogical, and chemical groups and tested for their efficiency for nitrate removal from aqueous solutions in the presence and absence of chloride ions. The incidence of graphene and nano zerovalent iron (Fe 0 ) in the nZVI-BC composite was confirmed by XRD. The nZVI-BC composite possessed highest surface area (220.92 m 2  g -1 ), carbon (80.55%), nitrogen (3.78%), and hydrogen (11.09%) contents compared to other materials. Nitrate sorption data was fitted well to the Langmuir (R 2  = 0.93-0.98) and Freundlich (R 2  = 0.90-0.99) isotherms. The sorption kinetics was adequately explained by the pseudo-second-order, power function, and Elovich models. The nZVI-BC composite showed highest Langmuir predicted sorption capacity (148.10 mg g -1 ) followed by EP-BC composite (72.77 mg g -1 ). In addition to the high surface area, the higher nitrate removal capacity of nZVI-BC composite could be attributed to the combination of two processes, i.e., chemisorption (outer-sphere complexation) and reduction of nitrate to ammonia or nitrogen by Fe 0 . The appearance of Fe-O stretching and N-H bonds in post-sorption FTIR spectra of nZVI-BC composite suggested the occurrence of redox reaction and formation of Fe compound with N, such as ferric nitrate (Fe(NO 3 ) 3 ·9H 2 O). Coexistence of chloride ions negatively influenced the nitrate sorption. The decrease in nitrate sorption with increasing chloride ion concentration was observed, which could be due to the competition of free active sites on the sorbents between nitrate and chloride ions. The nZVI-BC composite exhibited higher nitrate removal efficiency compared to other materials even in the presence of highest concentration (100 mg L -1 ) of coexisting chloride ion.

Quantifying sources of black carbon in western North America using observationally based analysis and an emission tagging technique in the Community Atmosphere Model

DOE PAGES

Zhang, Rudong; Wang, Hailong; Hegg, D. A.; ...

2015-11-18

The Community Atmosphere Model (CAM5), equipped with a technique to tag black carbon (BC) emissions by source regions and types, has been employed to establish source–receptor relationships for atmospheric BC and its deposition to snow over western North America. The CAM5 simulation was conducted with meteorological fields constrained by reanalysis for year 2013 when measurements of BC in both near-surface air and snow are available for model evaluation. We find that CAM5 has a significant low bias in predicted mixing ratios of BC in snow but only a small low bias in predicted atmospheric concentrations over northwestern USA and westernmore » Canada. Even with a strong low bias in snow mixing ratios, radiative transfer calculations show that the BC-in-snow darkening effect is substantially larger than the BC dimming effect at the surface by atmospheric BC. Local sources contribute more to near-surface atmospheric BC and to deposition than distant sources, while the latter are more important in the middle and upper troposphere where wet removal is relatively weak. Fossil fuel (FF) is the dominant source type for total column BC burden over the two regions. FF is also the dominant local source type for BC column burden, deposition, and near-surface BC, while for all distant source regions combined the contribution of biomass/biofuel (BB) is larger than FF. An observationally based positive matrix factorization (PMF) analysis of the snow-impurity chemistry is conducted to quantitatively evaluate the CAM5 BC source-type attribution. Furthermore, while CAM5 is qualitatively consistent with the PMF analysis with respect to partitioning of BC originating from BB and FF emissions, it significantly underestimates the relative contribution of BB. In addition to a possible low bias in BB emissions used in the simulation, the model is likely missing a significant source of snow darkening from local soil found in the observations.« less

Impacts of global, regional, and sectoral black carbon emission reductions on surface air quality and human mortality

NASA Astrophysics Data System (ADS)

Anenberg, S. C.; Talgo, K.; Arunachalam, S.; Dolwick, P.; Jang, C.; West, J. J.

2011-04-01

As a component of fine particulate matter (PM2.5), black carbon (BC) is associated with premature human mortality. BC also affects climate by absorbing solar radiation and reducing planetary albedo. Several studies have examined the climate impacts of BC emissions, but the associated health impacts have been studied less extensively. Here, we examine the surface PM2.5 and premature mortality impacts of halving anthropogenic BC emissions globally, from eight world regions, and from three major economic sectors. We use a global chemical transport model, MOZART-4, to simulate PM2.5 concentrations and a health impact function to calculate premature cardiopulmonary and lung cancer deaths. We estimate that halving global anthropogenic BC emissions reduces outdoor population-weighted average PM2.5 by 542 ng m-3 (1.8%) and avoids 157 000 (95% confidence interval, 120 000-194 000) annual premature deaths globally, with the vast majority occurring within the source region. While most of these avoided deaths can be achieved by halving East Asian emissions (54%), followed by South Asian emissions (31%), South Asian emissions have 50% greater mortality impacts per unit BC emitted than East Asian emissions. Globally, the contribution of residential, industrial, and transportation BC emissions to PM2.5-related mortality is 1.3, 1.2, and 0.6 times each sector's contribution to anthropogenic BC emissions, owing to the degree of co-location with population. Impacts of residential BC emissions are underestimated since indoor PM2.5 exposure is excluded. We estimate ~8 times more avoided deaths when BC and organic carbon (OC) emissions are halved together, suggesting that these results greatly underestimate the full air pollution-related mortality benefits of BC mitigation strategies which generally decrease both BC and OC. Confidence in our results would be strengthened by reducing uncertainties in emissions, model parameterization of aerosol processes, grid resolution, and PM2.5 concentration-mortality relationships globally.

Change in diurnal variations of meteorological variables induced by anthropogenic aerosols over the North China Plain in summer 2008

NASA Astrophysics Data System (ADS)

Gao, Yi; Zhang, Meigen; Liu, Xiaohong; Wang, Lili

2016-04-01

This study investigates the impacts of all anthropogenic aerosols and anthropogenic black carbon (BC) on the diurnal variations of meteorological variables in the atmospheric boundary layer over the North China Plain (NCP) during June to August 2008, using a coupled meteorology and chemistry model (WRF-Chem). The results of the ensemble numerical experiments show that surface air temperature decreases by about 0.6 to 1.2 K with the maximum decrease over the Beijing urban area and the southern part of Hebei province, and the surface relative humidity (RH) increases by 2-4 % owing to all anthropogenic aerosols. On the contrary, anthropogenic BC induces a small change of temperature and RH at surface. Averaged for Beijing, Tianjin, and Hebei province (BTH region) and High Particle Concentration (HPC) periods when PM2.5 surface concentration is more than 60 μg m-3 and daily AOD is more than 0.9, all anthropogenic aerosols decrease air temperature under 850 hPa and increase it between 500 and 850 hPa, while anthropogenic BC increases it for whole atmosphere. The maximum changes occur at 08:00-20:00 (local time). Aerosol-induced surface energy and diabatic heating change leads to a cooling at the surface and in the lower atmosphere and a warming in the middle troposphere at 08:00-17:00, with reversed effects at 20:00-05:00. BC cools the atmosphere at the surface and warms the atmosphere above for the whole day. As a result, the equivalent potential temperature profile change shows that the lower atmosphere is more stable at 08:00 and 14:00. All anthropogenic aerosols decrease the surface wind speed by 20-60 %, while anthropogenic BC decreases the wind speed by 10-40 % over the NCP with the maximum decrease at 08:00. The aerosol-induced stabilization of the lower atmosphere favors the accumulation of air pollutants and thus contributes to deterioration of visibility and fog-haze events.

An insight into the adsorption of diclofenac on different biochars: Mechanisms, surface chemistry, and thermodynamics.

PubMed

Lonappan, Linson; Rouissi, Tarek; Kaur Brar, Satinder; Verma, Mausam; Surampalli, Rao Y

2018-02-01

Biochars were prepared from feedstocks pinewood and pig manure. Biochar microparticles obtained through grinding were evaluated for the removal of emerging contaminant diclofenac (DCF) and the underlying mechanism were thoroughly studied. Characterization of biochar was carried out using particle size analyzer, SEM, BET, FT-IR, XRD, XPS and zeta potential instrument. Pig manure biochar (BC-PM) exhibited excellent removal efficiency (99.6%) over pine wood biochar (BC-PW) at 500 µg L -1 of DCF (environmentally significant concentration). Intraparticle diffusion was found to be the major process facilitated the adsorption. BC-PW followed pseudo first-order kinetics whereas BC-PM followed pseudo second-order kinetics. Pine wood biochar was largely affected by pH variations whereas for pig manure biochar, pH effects were minimal owing to its surface functional groups and DCF hydrophobicity. Thermodynamics, presence of co-existing ions, initial adsorbate concentration and particles size played substantial role in adsorption. Various isotherms models were also studied and results are presented. Copyright © 2017 Elsevier Ltd. All rights reserved.

In-situ measurements of light-absorbing impurities in snow of glacier on Mt. Yulong and implications for radiative forcing estimates.

PubMed

Niu, Hewen; Kang, Shichang; Shi, Xiaofei; Paudyal, Rukumesh; He, Yuanqing; Li, Gang; Wang, Shijin; Pu, Tao; Shi, Xiaoyi

2017-03-01

The Tibetan Plateau (TP) or the third polar cryosphere borders geographical hotspots for discharges of black carbon (BC). BC and dust play important roles in climate system and Earth's energy budget, particularly after they are deposited on snow and glacial surfaces. BC and dust are two kinds of main light-absorbing impurities (LAIs) in snow and glaciers. Estimating concentrations and distribution of LAIs in snow and glacier ice in the TP is of great interest because this region is a global hotspot in geophysical research. Various snow samples, including surface aged-snow, superimposed ice and snow meltwater samples were collected from a typical temperate glacier on Mt. Yulong in the snow melt season in 2015. The samples were determined for BC, Organic Carbon (OC) concentrations using an improved thermal/optical reflectance (DRI Model 2001) method and gravimetric method for dust concentrations. Results indicated that the LAIs concentrations were highly elevation-dependent in the study area. Higher contents and probably greater deposition at relative lower elevations (generally <5000masl) of the glacier was observed. Temporal difference of LAIs contents demonstrated that LAIs in snow of glacier gradually increased as snow melting progressed. Evaluations of the relative absorption of BC and dust displayed that the impact of dust on snow albedo and radiative forcing (RF) is substantially larger than BC, particularly when dust contents are higher. This was verified by the absorption factor, which was <1.0. In addition, we found the BC-induced albedo reduction to be in the range of 2% to nearly 10% during the snow melting season, and the mean snow albedo reduction was 4.63%, hence for BC contents ranging from 281 to 894ngg -1 in snow of a typical temperate glacier on Mt. Yulong, the associated instantaneous RF will be 76.38-146.96Wm -2 . Further research is needed to partition LAIs induced glacial melt, modeling researches in combination with long-term in-situ observations of LAIs in glaciers is also urgent needed in the future work. Copyright © 2017 Elsevier B.V. All rights reserved.

Tethered balloon-based black carbon profiles within the lower troposphere of Shanghai in the 2013 East China smog

NASA Astrophysics Data System (ADS)

Li, Juan; Fu, Qingyan; Huo, Juntao; Wang, Dongfang; Yang, Wen; Bian, Qinggen; Duan, Yusen; Zhang, Yihua; Pan, Jun; Lin, Yanfen; Huang, Kan; Bai, Zhipeng; Wang, Sheng-Hsiang; Fu, Joshua S.; Louie, Peter K. K.

2015-12-01

A Tethered balloon-based field campaign was launched for the vertical observation of air pollutants within the lower troposphere of 1000 m for the first time over a Chinese megacity, Shanghai in December of 2013. A custom-designed instrumentation platform for tethered balloon observation and ground-based observation synchronously operated for the measurement of same meteorological parameters and typical air pollutants. One episodic event (December 13) was selected with specific focus on particulate black carbon, a short-lived climate forcer with strong warming effect. Diurnal variation of the mixing layer height showed very shallow boundary of less than 300 m in early morning and night due to nocturnal inversion while extended boundary of more than 1000 m from noon to afternoon. Wind profiles showed relatively stagnant synoptic condition in the morning, frequent shifts between upward and downward motion at noon and in the afternoon, and dominant downward motion with sea breeze in the evening. Characteristics of black carbon vertical profiles during four different periods of a day were analyzed and compared. In the morning, surface BC concentration averaged as high as 20 μg/m3 due to intense traffic emissions from the morning rush hours and unfavorable meteorological conditions. A strong gradient of BC concentrations with altitude was observed from the ground to the top of boundary layer at around 250-370 m. BC gradients turned much smaller above the boundary layer. BC profiles measured during noon and afternoon were the least dependent on heights. The largely extended boundary layer with strong vertical convection was responsible for a well mixing of BC particles in the whole measured column. BC profiles were similar between the early-evening and late-evening phases. The lower troposphere was divided into two stratified air layers with contrasted BC vertical distributions. Profiles at night showed strong gradients from the relatively high surface concentrations to low concentrations near the top of the boundary layer around 200 m. Above the boundary layer, BC increased with altitudes and reached a maximum at the top of 1000 m. Prevailing sea breeze within the boundary layer was mainly responsible for the quick cleanup of BC in the lower altitudes. In contrast, continental outflow via regional transport was the major cause of the enhanced BC aloft. This study provides a first insight of the black carbon vertical profiles over Eastern China, which will have significant implications for narrowing the gaps between the source emissions and observations as well as improving estimations of BC radiative forcing and regional climate.

CCN concentrations and BC warming influenced by maritime ship emitted aerosol plumes over southern Bay of Bengal.

PubMed

Ramana, M V; Devi, Archana

2016-08-02

Significant quantities of carbon soot aerosols are emitted into pristine parts of the atmosphere by marine shipping. Soot impacts the radiative balance of the Earth-atmosphere system by absorbing solar-terrestrial radiation and modifies the microphysical properties of clouds. Here we examined the impact of black carbon (BC) on net warming during monsoon season over southern Bay-of-Bengal, using surface and satellite measurements of aerosol plumes from shipping. Shipping plumes had enhanced the BC concentrations by a factor of four around the shipping lane and exerted a strong positive influence on net warming. Compiling all the data, we show that BC atmospheric heating rates for relatively-clean and polluted-shipping corridor locations to be 0.06 and 0.16 K/day respectively within the surface layer. Emissions from maritime ships had directly heated the lower troposphere by two-and-half times and created a gradient of around 0.1 K/day on either side of the shipping corridor. Furthermore, we show that ship emitted aerosol plumes were responsible for increase in the concentration of cloud condensation nuclei (CCN) by an order of magnitude that of clean air. The effects seen here may have significant impact on the monsoonal activity over Bay-of-Bengal and implications for climate change mitigation strategies.

Source sector and region contributions to BC and PM 2.5 in Central Asia

DOE PAGES

Kulkarni, S.; Sobhani, N.; Miller-Schulze, J. P.; ...

2015-02-18

Particulate matter (PM) mass concentrations, seasonal cycles, source sector, and source region contributions in Central Asia (CA) are analyzed for the period April 2008–July 2009 using the Sulfur Transport and dEposition Model (STEM) chemical transport model and modeled meteorology from the Weather Research and Forecasting (WRF) model. Predicted aerosol optical depth (AOD) values (annual mean value ~0.2) in CA vary seasonally, with lowest values in the winter. Surface PM 2.5 concentrations (annual mean value ~10 μg m −3) also exhibit a seasonal cycle, with peak values and largest variability in the spring/summer, and lowest values and variability in the wintermore » (hourly values from 2 to 90 μg m −3). Surface concentrations of black carbon (BC) (mean value ~0.1 μg m −3) show peak values in the winter. The simulated values are compared to surface measurements of AOD as well as PM 2.5, PM 10, BC, and organic carbon (OC) mass concentrations at two regional sites in Kyrgyzstan (Lidar Station Teplokluchenka (LST) and Bishkek). The predicted values of AOD and PM mass concentrations and their seasonal cycles are fairly well captured. The carbonaceous aerosols are underpredicted in winter, and analysis suggests that the winter heating emissions are underestimated in the current inventory. Dust, from sources within and outside CA, is a significant component of the PM mass and drives the seasonal cycles of PM and AOD. On an annual basis, the power and industrial sectors are found to be the most important contributors to the anthropogenic portion of PM 2.5. Residential combustion and transportation are shown to be the most important sectors for BC. Biomass burning within and outside the region also contributes to elevated PM and BC concentrations. The analysis of the transport pathways and the variations in particulate matter mass and composition in CA demonstrates that this region is strategically located to characterize regional and intercontinental transport of pollutants. Aerosols at these sites are shown to reflect dust, biomass burning, and anthropogenic sources from Europe; South, East, and Central Asia; and Russia depending on the time period. Simulations for a reference 2030 emission scenario based on pollution abatement measures already committed to in current legislation show that PM 2.5 and BC concentrations in the region increase, with BC growing more than PM 2.5 on a relative basis. This indicates that both the health impacts and the climate warming associated with these particles may increase over the next decades unless additional control measures are taken. The importance of observations in CA to help characterize the changes that are rapidly taking place in the region are discussed.« less

Source Estimation of Wintertime Soot Particles for an Urban Site Varanasi (25.30 N, 83.00 E) in Central Indo-Gangetic Plain Region

NASA Astrophysics Data System (ADS)

Singh, A. K.; Srivastava, M. K.; Dumka, U. C.; Singh, R. K.; Singh, R. S.; Tiwari, S.; Mehrotra, B. J.; Srivastava, A. K.

2017-12-01

Black carbon particles (BC: also called Soot) are formed by incomplete combustion of hydrocarbon based fuels (fossil fuel: coal, diesel, petrol, etc.) as well as due to burning of biomass and bio-fuels (wood, shrubs, dry leaves, etc.). Soot particles are warming agent to the atmosphere that gained wide attention in recent years due to their direct and indirect impacts on local, regional as well as global climate. The climatic effects due to soot are not well understood as indicated by large uncertainties in their climate forcing estimation, particularly in South and East Asian region, possibly due to unavailability of adequate database and information about the source. Measurement of wintertime BC mass concentrations for urban site in central IGP, `Varanasi' (25.30 N, 83.00 E), using a seven wavelength Aethalometer is reported in this work. Delta-C (=BC370 - BC880), which is an indicator of biomass/bio-fuels or residential coal burning is used to understand the source. Aethalometer based source apportionment model "Aethalometer model" was used to apportion the fossil fuel/traffic and wood/biomass burning mass concentration to the total BC mass. The preliminary results for representative month (January-2015) show that daily-average BC mass ranged from 4.47 to 20.70 μg m-3 (Average: 9.45 ± 4.15 μg m-3). The daily Absorption Ångström Exponent (AAE) and the ratio of BCff/BC and BCff/BCwb varied between 1.09 - 1.32, 0.67 - 0.92 and 2 - 40, respectively, due to the changes in BC emissions rates. The total BC, BC from fossil fuel (BCff) and BC from wood/biomass burning (BCwb) behaved in the remarkable diurnal pattern, behaving opposite to the mixing layer heights (MLHs). During daytime, MLHs are higher due to surface based solar warming and causes more volume of atmosphere for the BC dispersion. This phenomenon causes the surface measurement of lower BC mass during the daytime. The data is, however, still being processed for multi-year wintertime observations and the detailed discussions will be shown during the presentation.

Enhanced Sorption of PAHs in Natural-Fire-Impacted Sediments from Oriole Lake, California

EPA Science Inventory

Surface sediment cores from Oriole Lake (CA) were analyzed for organic carbon (OC), black carbon (BC), and their δ13C isotope ratios. Sediments displayed high OC(20-25%) and increasing BC concentrations from ∼0.40% (in 1800 C.E.) to ∼0.60% dry weight (in 2000 C.E.). Petrographic...

Rapid Adjustments Cause Weak Surface Temperature Response to Increased Black Carbon Concentrations

NASA Astrophysics Data System (ADS)

Stjern, Camilla Weum; Samset, Bjørn Hallvard; Myhre, Gunnar; Forster, Piers M.; Hodnebrog, Øivind; Andrews, Timothy; Boucher, Olivier; Faluvegi, Gregory; Iversen, Trond; Kasoar, Matthew; Kharin, Viatcheslav; Kirkevâg, Alf; Lamarque, Jean-François; Olivié, Dirk; Richardson, Thomas; Shawki, Dilshad; Shindell, Drew; Smith, Christopher J.; Takemura, Toshihiko; Voulgarakis, Apostolos

2017-11-01

We investigate the climate response to increased concentrations of black carbon (BC), as part of the Precipitation Driver Response Model Intercomparison Project (PDRMIP). A tenfold increase in BC is simulated by nine global coupled-climate models, producing a model median effective radiative forcing of 0.82 (ranging from 0.41 to 2.91) W m-2, and a warming of 0.67 (0.16 to 1.66) K globally and 1.24 (0.26 to 4.31) K in the Arctic. A strong positive instantaneous radiative forcing (median of 2.10 W m-2 based on five of the models) is countered by negative rapid adjustments (-0.64 W m-2 for the same five models), which dampen the total surface temperature signal. Unlike other drivers of climate change, the response of temperature and cloud profiles to the BC forcing is dominated by rapid adjustments. Low-level cloud amounts increase for all models, while higher-level clouds are diminished. The rapid temperature response is particularly strong above 400 hPa, where increased atmospheric stabilization and reduced cloud cover contrast the response pattern of the other drivers. In conclusion, we find that this substantial increase in BC concentrations does have considerable impacts on important aspects of the climate system. However, some of these effects tend to offset one another, leaving a relatively small median global warming of 0.47 K per W m-2—about 20% lower than the response to a doubling of CO2. Translating the tenfold increase in BC to the present-day impact of anthropogenic BC (given the emissions used in this work) would leave a warming of merely 0.07 K.

Higher Atmosphere Heating due to black carbon Over the Northern Part of India

NASA Astrophysics Data System (ADS)

Tiwari, S.; Singh, S., , Dr

2017-12-01

Light-absorbing, atmospheric particles have gained greater attention in recent years because of their direct and indirect impacts on regional and global climate. Atmospheric black carbon (BC) aerosol (also called soot particle) is a leading climate warming agent, yet uncertainties in the global direct aerosol radiative forcing remain large. Based on a year of aerosol absorption measurements at seven wavelengths, BC concentrations were investigated in Dhanbad, the coal capital of India. Coal is routinely burned for cooking and residential heat as well as in small industries. The mean daily concentrations of ultraviolet-absorbing black carbon measured at 370 nm (UVBC) and black carbon measured at 880 nm (BC) were 9.8 ± 5.7 and 6.5 ± 3.8 μg m-3, respectively. The difference between UVBC and BC, Delta-C, is an indicator of biomass or residential coal burning and averaged 3.29 ± 4.61 μg m-3. An alternative approach uses the calculation of the Angstrom Exponent (AE) to estimate the amounts of biomass/coal and traffic BC. Biomass/coal burning contributed 87% and fossil fuel combustion contributed 13% to the annual average BC concentration. In the post-monsoon season, potential source contribution function analysis showed that air masses came from the central and northwestern Indo-Gangetic Plains resulting in mean UVBC values of 10.9 μg m-3 and BC of 7.2 μg m-3. The mean winter UVBC and BC concentrations were 15.0 and 10.1 μg m-3, respectively. These highest values were largely driven by local sources under conditions of poor dispersion. The direct radiative forcing (DRF) due to UVBC and BC at the surface (SFC) and the top of the atmosphere (TOA) were calculated. The mean atmospheric heating rates due to UVBC and BC were estimated to be 1.40°K day-1 and 1.18°K day-1, respectively. This high heating rate may affect the monsoon circulation in this region.

Source region and sector contributions of atmospheric soot particle in a coalfield region of Dhanbad, eastern part of India

NASA Astrophysics Data System (ADS)

Singh, S.; Tiwari, S.; Dumka, U. C.; Kumar, R.; Singh, P. K.

2017-11-01

Black carbon (BC) aerosols affect the Earth's climate directly by interacting with the solar radiation and indirectly by modifying the lifetime and optical properties of clouds. However, our understanding of BC aerosols and their impacts on the climate are limited by lack of in situ measurements of BC, especially in the developing world. This study reports measurements of BC from Dhanbad, a coalfields area of eastern India, we analyze BC data at 370 and 880 nm during 2013 to gain insight into the emission sources affecting the study area. Our analysis indicates significantly higher absorption at the lower wavelength (ultraviolet). We estimate that 33% of BC at Dhanbad comes from biomass/biofuel combustion and the remaining 67% from the fossil fuel combustion. Higher concentrations of BC370 nm (> 12 μg m- 3) were observed when the air masses affecting Dhanbad originated far away in countries like Iran, Afghanistan, Pakistan, Oman, United Arab Emirates and passed over the Indo-Gangetic Plains (IGP) prior to arriving at the observation site. The source regions affecting BC880 nm were localized over the IGP but BC880 nm concentrations are 33% lower ( 8 μg m- 3) than BC370 nm. The cluster analysis showed that the largest fraction (35 and 29%) of the air masses arriving at Dhanbad passed through the boundary layer of the central IGP and north-west IGP region during the post-monsoon season. Average values of BC370 nm (16.0 and 20.0 μg m- 3) and BC880 nm (9.5 and 10.0 μg m- 3) in the IGP influenced air masses were significantly higher than those arriving from other source regions. The Weather Research and Forecasting model coupled with Chemistry (WRF-Chem) model were applied to understand the relative importance of different sources affecting Dhanbad. The variability of observed BC mass concentrations was captured fairly well by WRF-Chem with minor deviations from the measured values. Model results indicate that anthropogenic emissions account for more than 75% of the surface BC at Dhanbad. Biomass burning contribution peaks in March-April and October-November but remains less than 25%. Long-range transport estimated in terms of inflow from domain boundaries does not affect BC concentrations at Dhanbad significantly.

Exposure to ultrafine particles and black carbon in diesel-powered commuter trains

NASA Astrophysics Data System (ADS)

Jeong, Cheol-Heon; Traub, Alison; Evans, Greg J.

2017-04-01

Ultrafine particle (UFP), black carbon (BC) and lung deposited surface area (LDSA) concentrations measured during 43 trips on diesel-powered commuter trains revealed elevated exposures under some conditions. When the passenger coaches were pulled by a locomotive, the geometric mean concentrations of UFP, LDSA, and BC were 18, 10, and 6 times higher than the exposure levels when the locomotive pushed the coaches, respectively. In addition, UFP, LDSA, and BC concentrations in pull-trains were 5, 3, and 4 times higher than concentrations measured while walking on city sidewalks, respectively. Exposure to these pollutants was most elevated in the coach located closest to the locomotive: geometric means were 126,000 # cm-3 for UFP, 249 μm2 cm-3 for LDSA, and 17,800 ng m-3 of BC; these concentrations are much higher than those previously reported for other modes of public transportation. Markedly high levels of diesel exhaust are present in passenger trains powered by diesel locomotives operated in pull-mode. Thus, it is recommended that immediate steps be taken to evaluate, and where needed, mitigate exposure in diesel-powered passenger trains, both commuter and inter-city.

Wintertime vertical variations in particulate matter (PM) and precursor concentrations in the San Joaquin Valley during the California Regional Coarse PM/Fine PM Air Quality Study.

PubMed

Brown, Steven G; Roberts, Paul T; McCarthy, Michael C; Lurmann, Frederick W; Hyslop, Nicole P

2006-09-01

Air quality monitoring was conducted at a rural site with a tower in the middle of California's San Joaquin Valley (SJV) and at elevated sites in the foothills and mountains surrounding the SJV for the California Regional PM10/ PM2.5 Air Quality Study. Measurements at the surface and n a tower at 90 m were collected in Angiola, CA, from December 2000 through February 2001 and included hourly black carbon (BC), particle counts from optical particle counters, nitric oxide, ozone, temperature, relative humidity, wind speed, and direction. Boundary site measurements were made primarily using 24-hr integrated particulate matter (PM) samples. These measurements were used to understand the vertical variations of PM and PM precursors, the effect of stratification in the winter on concentrations and chemistry aloft and at the surface, and the impact of aloft-versus-surface transport on PM concentrations. Vertical variations of concentrations differed among individual species. The stratification may be important to atmospheric chemistry processes, particularly nighttime nitrate formation aloft, because NO2 appeared to be oxidized by ozone in the stratified aloft layer. Additionally, increases in accumulation-mode particle concentrations in the aloft layer during a fine PM (PM2.5) episode corresponded with increases in aloft nitrate, demonstrating the likelihood of an aloft nighttime nitrate formation mechanism. Evidence of local transport at the surface and regional transport aloft was found; transport processes also varied among the species. The distribution of BC appeared to be regional, and BC was often uniformly mixed vertically. Overall, the combination of time-resolved tower and surface measurements provided important insight into PM stratification, formation, and transport.

Description and evaluation of a new four-mode version of the Modal Aerosol Module (MAM4) within version 5.3 of the Community Atmosphere Model

NASA Astrophysics Data System (ADS)

Liu, X.; Ma, P.-L.; Wang, H.; Tilmes, S.; Singh, B.; Easter, R. C.; Ghan, S. J.; Rasch, P. J.

2016-02-01

Atmospheric carbonaceous aerosols play an important role in the climate system by influencing the Earth's radiation budgets and modifying the cloud properties. Despite the importance, their representations in large-scale atmospheric models are still crude, which can influence model simulated burden, lifetime, physical, chemical and optical properties, and the climate forcing of carbonaceous aerosols. In this study, we improve the current three-mode version of the Modal Aerosol Module (MAM3) in the Community Atmosphere Model version 5 (CAM5) by introducing an additional primary carbon mode to explicitly account for the microphysical ageing of primary carbonaceous aerosols in the atmosphere. Compared to MAM3, the four-mode version of MAM (MAM4) significantly increases the column burdens of primary particulate organic matter (POM) and black carbon (BC) by up to 40 % in many remote regions, where in-cloud scavenging plays an important role in determining the aerosol concentrations. Differences in the column burdens for other types of aerosol (e.g., sulfate, secondary organic aerosols, mineral dust, sea salt) are less than 1 %. Evaluating the MAM4 simulation against in situ surface and aircraft observations, we find that MAM4 significantly improves the simulation of seasonal variation of near-surface BC concentrations in the polar regions, by increasing the BC concentrations in all seasons and particularly in cold seasons. However, it exacerbates the overestimation of modeled BC concentrations in the upper troposphere in the Pacific regions. The comparisons suggest that, to address the remaining model POM and BC biases, future improvements are required related to (1) in-cloud scavenging and vertical transport in convective clouds and (2) emissions of anthropogenic and biomass burning aerosols.

Description and evaluation of a new four-mode version of the Modal Aerosol Module (MAM4) within version 5.3 of the Community Atmosphere Model

DOE PAGES

Liu, X.; Ma, P. -L.; Wang, H.; ...

2016-02-08

Atmospheric carbonaceous aerosols play an important role in the climate system by influencing the Earth's radiation budgets and modifying the cloud properties. Despite the importance, their representations in large-scale atmospheric models are still crude, which can influence model simulated burden, lifetime, physical, chemical and optical properties, and the climate forcing of carbonaceous aerosols. In this study, we improve the current three-mode version of the Modal Aerosol Module (MAM3) in the Community Atmosphere Model version 5 (CAM5) by introducing an additional primary carbon mode to explicitly account for the microphysical ageing of primary carbonaceous aerosols in the atmosphere. Compared to MAM3,more » the four-mode version of MAM (MAM4) significantly increases the column burdens of primary particulate organic matter (POM) and black carbon (BC) by up to 40 % in many remote regions, where in-cloud scavenging plays an important role in determining the aerosol concentrations. Differences in the column burdens for other types of aerosol (e.g., sulfate, secondary organic aerosols, mineral dust, sea salt) are less than 1 %. Evaluating the MAM4 simulation against in situ surface and aircraft observations, we find that MAM4 significantly improves the simulation of seasonal variation of near-surface BC concentrations in the polar regions, by increasing the BC concentrations in all seasons and particularly in cold seasons. However, it exacerbates the overestimation of modeled BC concentrations in the upper troposphere in the Pacific regions. As a result, the comparisons suggest that, to address the remaining model POM and BC biases, future improvements are required related to (1) in-cloud scavenging and vertical transport in convective clouds and (2) emissions of anthropogenic and biomass burning aerosols.« less

An AeroCom Assessment of Black Carbon in Arctic Snow and Sea Ice

NASA Technical Reports Server (NTRS)

Jiao, C.; Flanner, M. G.; Balkanski, Y.; Bauer, S. E.; Bellouin, N.; Bernsten, T. K.; Bian, H.; Carslaw, K. S.; Chin, M.; DeLuca, N.;

Ambient black carbon particulate matter in the coal region of Dhanbad, India.

PubMed

Singh, S; Tiwari, S; Hopke, P K; Zhou, C; Turner, J R; Panicker, A S; Singh, P K

2018-02-15

Light-absorbing, atmospheric particles have gained greater attention in recent years because of their direct and indirect impacts on regional and global climate. Atmospheric black carbon (BC) aerosol is a leading climate warming agent, yet uncertainties in the global direct aerosol radiative forcing remain large. Based on a year of aerosol absorption measurements at seven wavelengths, BC concentrations were investigated in Dhanbad, the coal capital of India. Coal is routinely burned for cooking and residential heat as well as in small industries. The mean daily concentrations of ultraviolet-absorbing black carbon measured at 370nm (UVBC) and black carbon measured at 880nm (BC) were 9.8±5.7 and 6.5±3.8μgm -3 , respectively. The difference between UVBC and BC, Delta-C, is an indicator of biomass or residential coal burning and averaged 3.29±4.61μgm -3 . An alternative approach uses the Ǻngstrom Exponent (AE) to estimate the biomass/coal and traffic BC concentrations. Biomass/coal burning contributed ~87% and high temperature, fossil-fuel combustion contributed ~13% to the annual average BC concentration. The post-monsoon seasonal mean UVBC values were 10.9μgm -3 and BC of 7.2μgm -3 . Potential source contribution function analysis showed that in the post-monsoon season, air masses came from the central and northwestern Indo-Gangetic Plains where there is extensive agricultural burning. The mean winter UVBC and BC concentrations were 15.0 and 10.1μgm -3 , respectively. These higher values were largely produced by local sources under poor dispersion conditions. The direct radiative forcing (DRF) due to UVBC and BC at the surface (SUR) and the top of the atmosphere (TOA) were calculated. The mean atmospheric heating rates due to UVBC and BC were estimated to be 1.40°Kday -1 and 1.18°Kday -1 , respectively. This high heating rate may affect the monsoon circulation in this region. Copyright © 2017 Elsevier B.V. All rights reserved.

Sources of springtime surface black carbon in the Arctic: an adjoint analysis for April 2008

NASA Astrophysics Data System (ADS)

Qi, Ling; Li, Qinbin; Henze, Daven K.; Tseng, Hsien-Liang; He, Cenlin

2017-08-01

We quantify source contributions to springtime (April 2008) surface black carbon (BC) in the Arctic by interpreting surface observations of BC at five receptor sites (Denali, Barrow, Alert, Zeppelin, and Summit) using a global chemical transport model (GEOS-Chem) and its adjoint. Contributions to BC at Barrow, Alert, and Zeppelin are dominated by Asian anthropogenic sources (40-43 %) before 18 April and by Siberian open biomass burning emissions (29-41 %) afterward. In contrast, Summit, a mostly free tropospheric site, has predominantly an Asian anthropogenic source contribution (24-68 %, with an average of 45 %). We compute the adjoint sensitivity of BC concentrations at the five sites during a pollution episode (20-25 April) to global emissions from 1 March to 25 April. The associated contributions are the combined results of these sensitivities and BC emissions. Local and regional anthropogenic sources in Alaska are the largest anthropogenic sources of BC at Denali (63 % of total anthropogenic contributions), and natural gas flaring emissions in the western extreme north of Russia (WENR) are the largest anthropogenic sources of BC at Zeppelin (26 %) and Alert (13 %). We find that long-range transport of emissions from Beijing-Tianjin-Hebei (also known as Jing-Jin-Ji), the biggest urbanized region in northern China, contribute significantly (˜ 10 %) to surface BC across the Arctic. On average, it takes ˜ 12 days for Asian anthropogenic emissions and Siberian biomass burning emissions to reach the Arctic lower troposphere, supporting earlier studies. Natural gas flaring emissions from the WENR reach Zeppelin in about a week. We find that episodic transport events dominate BC at Denali (87 %), a site outside the Arctic front, which is a strong transport barrier. The relative contribution of these events to surface BC within the polar dome is much smaller (˜ 50 % at Barrow and Zeppelin and ˜ 10 % at Alert). The large contributions from Asian anthropogenic sources are predominately in the form of chronic pollution (˜ 40 % at Barrow, 65 % at Alert, and 57 % at Zeppelin) on about a 1-month timescale. As such, it is likely that previous studies using 5- or 10-day trajectory analyses strongly underestimated the contribution from Asia to surface BC in the Arctic.

Enhanced Solar Energy Absorption by Internally-mixed Black Carbon in Snow Grains

DOE Office of Scientific and Technical Information (OSTI.GOV)

Flanner, M. G.; Liu, Xiaohong; Zhou, Cheng

2012-05-30

Here we explore light absorption by snowpack containing black carbon (BC) particles residing within ice grains. Basic considerations of particle volumes and BC/snow mass concentrations show that there are generally 0:05-109 BC particles for each ice grain. This suggests that internal BC is likely distributed as multiple inclusions within ice grains, and thus the dynamic effective medium approximation (DEMA) (Chylek and Srivastava, 1983) is a more appropriate optical representation for BC/ice composites than coated-sphere or standard mixing approximations. DEMA calculations show that the 460 nm absorption cross-section of BC/ice composites, normalized to the mass of BC, is typically enhanced bymore » factors of 1.8-2.1 relative to interstitial BC. BC effective radius is the dominant cause of variation in this enhancement, compared with ice grain size and BC volume fraction. We apply two atmospheric aerosol models that simulate interstitial and within-hydrometeor BC lifecycles. Although only {approx}2% of the atmospheric BC burden is cloud-borne, 71-83% of the BC deposited to global snow and sea-ice surfaces occurs within hydrometeors. Key processes responsible for within-snow BC deposition are development of hydrophilic coatings on BC, activation of liquid droplets, and subsequent snow formation through riming or ice nucleation by other species and aggregation/accretion of ice particles. Applying deposition fields from these aerosol models in offline snow and sea-ice simulations, we calculate that 32-73% of BC in global surface snow resides within ice grains. This fraction is smaller than the within-hydrometeor deposition fraction because meltwater flux preferentially removes internal BC, while sublimation and freezing within snowpack expose internal BC. Incorporating the DEMA into a global climate model, we simulate increases in BC/snow radiative forcing of 43-86%, relative to scenarios that apply external optical properties to all BC. We show that snow metamorphism driven by diffusive vapor transfer likely proceeds too slowly to alter the mass of internal BC while it is radiatively active, but neglected processes like wind pumping and convection may play much larger roles. These results suggest that a large portion of BC in surface snowpack may reside within ice grains and increase BC/snow radiative forcing, although measurements to evaluate this are lacking. Finally, previous studies of BC/snow forcing that neglected this absorption enhancement are not necessarily biased low, because of application of absorption-enhancing sulfate coatings to hydrophilic BC, neglect of coincident absorption by dust in snow, and implicit treatment of cloud-borne BC resulting in longer-range transport.« less

Evaluations of the Method to Measure Black Carbon Particles Suspended in Rainwater and Snow Samples

NASA Astrophysics Data System (ADS)

Ohata, S.; Moteki, N.; Schwarz, J. P.; Fahey, D. W.; Kondo, Y.

2012-12-01

The mass concentrations and size distributions of black carbon (BC) particles in rainwater and snow are important parameters for improved understanding of the wet deposition of BC, is a key process in quantifying the impacts of BC on climate. In this study, we have evaluated a new method to measure these parameters. The approach consists of an ultrasonic nebulizer (USN) used in conjunction with a Single Particle Soot Photometer (SP2). The USN converts sample water into micron-size droplets at a constant rate and then extracts airborne BC particles by dehydrating the water droplets. The mass of individual BC particles is measured by the SP2, based on the laser-induced incandescence technique. The combination of the USN and SP2 enabled the measurement of BC particles using only small amount of sample water, typically 10 ml (Ohata et al., 2011). However, the loss of BC during the extraction process depends on their size. We determined the size-dependent extraction efficiency using polystyrene latex spheres (PSLs) with twelve different diameters between 100-1050 nm. The PSL concentrations in water were determined by the light extinction of at 532nm. The extraction efficiency of the USN showed broad maximum in the diameter range of 200-500nm, and decreased substantially at larger sizes. The extraction efficiency determined using the PSL standards agreed to within ±40% with that determined using laboratory-generated BC concentration standards. We applied this method to the analysis of rainwater collected in Tokyo and Okinawa over the East China Sea. Measured BC size distributions in all rainwater samples showed negligible contribution of the BC particles larger than 600nm to the total BC amounts. However, for BC particles in surface snow collected in Greenland and Antarctica, size distributions were sometimes shifted to much larger size ranges.

Estimation of columnar concentrations of absorbing and scattering fine mode aerosol components using AERONET data

NASA Astrophysics Data System (ADS)

Choi, Yongjoo; Ghim, Young Sung

2016-11-01

Columnar concentrations of absorbing and scattering components of fine mode aerosols were estimated using Aerosol Robotic Network (AERONET) data for a site downwind of Seoul. The study period was between March 2012 and April 2013 including the period of the Distributed Regional Aerosol Gridded Observation Networks (DRAGON)-Asia campaign in March to May 2012. The Maxwell Garnett mixing rule was assumed for insoluble components embedded in a host solution, while the volume average mixing rule was assumed for the aqueous solution of soluble components. During the DRAGON-Asia campaign the surface concentrations of major components of fine particles were measured. The columnar mass fractions of black carbon (BC), organic carbon (OC), mineral dust (MD), and ammonium sulfate (AS) were 1.5, 5.9, 6.6, and 52%, respectively, which were comparable to the mass fractions measured at the surface for BC, OC, and secondary inorganic aerosols at 2.3, 18, and 55%. The vertical distributions of BC and AS were investigated by employing the concept of a column height. While the column height for BC was similar to the planetary boundary layer (PBL) height, that for AS was 4.4 times higher than the PBL height and increased with air temperature from March to May. The monthly variations of the columnar mass concentrations during the study period were generally well explained in term of meteorology and emission characteristics. However, certain variations of MD were different from those typically observed primarily because only fine mode aerosols were considered.

Transport of particle pollution into the Maipo Valley: winter 2015 campaign results

NASA Astrophysics Data System (ADS)

Huneeus, Nicolás; Mazzeo, Andrea; Ordóñez, César; Donoso, Nicolás; Gallardo, Laura; Molina, Luisa; Moreno, Valeria; Muñoz, Ricardo; Orfanoz, Andrea; Vizcarra, Aldo

2016-04-01

Each winter, Santiago (33° 27'S, 70° 40'W) the capital of Chile with a population of about 7 million people, experiences episodes with particulate matter (PM) concentrations larger than allowed by Chilean environmental regulations. Transport and residential heating largely dominate emissions prior to and during these episodes. Important impact of black carbon (BC) on the cryosphere has been documented in other parts of the world associated with urban pollution. In order to explore if BC from Santiago has the potential to reach the Andean cryosphere during the aforementioned episodes, a one week-long campaign was conducted in Santiago and the Maipo Valley between 18th and 25th of July 2015 when the air quality conditions of the city reached twice the critical levels (pre-emergency in Chilean regulations). Measurements were carried out at three sites: downtown Santiago, the entrance of the valley (and outskirts of Santiago) and 12 km inside the Maipo Valley. At each of these sites both surface and vertically distributed measurements were conducted. A meteorological station measuring standard meteorological parameters and an E-Sampler measuring PM10 concentrations were installed at each site. In addition, a tethered balloon equipped with a sonde and a mini-aethalometer was used in each site to measure vertical profiles of standard meteorological parameters and BC concentrations, respectively. The tethered balloon was raised every three hours up to a maximum of 1000 meters above ground level, whenever meteorological conditions allowed. In general, the BC concentrations inside the valley, both at the surface and in the vertical, were dominated by emissions within the valley and BC was limited to shallow layers above the ground. However, on both days with critical air quality levels, winds blowing from the city and deeper BC layers were observed inside the valley. Furthermore, during these days observations at the entrance of the valley and those taken inside were coupled, contrary to the other days when they were decoupled. This deeper BC layer and the coupling of observations at the entrance and inside the valley suggest that pollutants are transported into the Maipo Valley and thus could potentially reach the snow and ice covered areas in the Andes.

Using an Explicit Emission Tagging Method in Global Modeling of Source-Receptor Relationships for Black Carbon in the Arctic: Variations, Sources and Transport Pathways

DOE Office of Scientific and Technical Information (OSTI.GOV)

Wang, Hailong; Rasch, Philip J.; Easter, Richard C.

2014-11-27

We introduce an explicit emission tagging technique in the Community Atmosphere Model to quantify source-region-resolved characteristics of black carbon (BC), focusing on the Arctic. Explicit tagging of BC source regions without perturbing the emissions makes it straightforward to establish source-receptor relationships and transport pathways, providing a physically consistent and computationally efficient approach to produce a detailed characterization of the destiny of regional BC emissions and the potential for mitigation actions. Our analysis shows that the contributions of major source regions to the global BC burden are not proportional to the respective emissions due to strong region-dependent removal rates and lifetimes,more » while the contributions to BC direct radiative forcing show a near-linear dependence on their respective contributions to the burden. Distant sources contribute to BC in remote regions mostly in the mid- and upper troposphere, having much less impact on lower-level concentrations (and deposition) than on burden. Arctic BC concentrations, deposition and source contributions all have strong seasonal variations. Eastern Asia contributes the most to the wintertime Arctic burden. Northern Europe emissions are more important to both surface concentration and deposition in winter than in summer. The largest contribution to Arctic BC in the summer is from Northern Asia. Although local emissions contribute less than 10% to the annual mean BC burden and deposition within the Arctic, the per-emission efficiency is much higher than for major non-Arctic sources. The interannual variability (1996-2005) due to meteorology is small in annual mean BC burden and radiative forcing but is significant in yearly seasonal means over the Arctic. When a slow aging treatment of BC is introduced, the increase of BC lifetime and burden is source-dependent. Global BC forcing-per-burden efficiency also increases primarily due to changes in BC vertical distributions. The relative contribution from major non-Arctic sources to the Arctic BC burden increases only slightly, although the contribution of Arctic local sources is reduced by a factor of 2 due to the slow aging treatment.« less

Top-down estimates of biomass burning emissions of black carbon in the western United States

Treesearch

Y. H. Mao; Q. B. Li; D. Chen; L. Zhang; W. -M. Hao; K.-N. Liou

2014-01-01

We estimate biomass burning and anthropogenic emissions of black carbon (BC) in the western US for May-October 2006 by inverting surface BC concentrations from the Interagency Monitoring of PROtected Visual Environment (IMPROVE) network using a global chemical transport model. We first use active fire counts from the Moderate Resolution Imaging Spectroradiometer (MODIS...

Constraining Black Carbon Aerosol over Asia using OMI Aerosol Absorption Optical Depth and the Adjoint of GEOS-Chem

NASA Technical Reports Server (NTRS)

Zhang, Li; Henze, David K.; Grell, Georg A.; Carmichael. Gregory R.; Bousserez, Nicolas; Zhang, Qiang; Torres, Omar; Ahn, Changwoo; Lu, Zifeng; Cao, Junji;

DOE Office of Scientific and Technical Information (OSTI.GOV)

Zinin, Pavel V.; Burgess, Katherine; Jia, Ruth

Dense BC{sub x} phases with high boron concentration are predicted to be metastable, superhard, and conductors or superconductors depending on boron concentration. However, up to this point, diamond-like boron rich carbides BC{sub x} (dl-BC{sub x}) phases have been thought obtainable only through high pressure and high temperature treatment, necessitating small specimen volume. Here, we use electron energy loss spectroscopy combined with transmission electron microscopy, Raman spectroscopy, surface Brillouin scattering, laser ultrasonics (LU) technique, and analysis of elastic properties to demonstrate that low pressure synthesis (chemical vapor deposition) of BC{sub x} phases may also lead to the creation of diamond-like boronmore » rich carbides. The elastic properties of the dl-BC{sub x} phases depend on the carbon sp²versus sp³ content, which decreases with increasing boron concentration, while the boron bonds determine the shape of the Raman spectra of the dl-BC{sub x} after high pressure-high temperature treatment. Using the estimation of the density value based on the sp³ fraction, the shear modulus μ of dl-BC₄, containing 10% carbon atoms with sp³ bonds, and dl-B₃C₂, containing 38% carbon atoms with sp³ bonds, were found to be μ = 19.3 GPa and μ = 170 GPa, respectively. The presented experimental data also imply that boron atoms lead to a creation of sp³ bonds during the deposition processes.« less

Plackett-Burman experimental design for bacterial cellulose-silica composites synthesis.

PubMed

Guzun, Anicuta Stoica; Stroescu, Marta; Jinga, Sorin Ion; Voicu, Georgeta; Grumezescu, Alexandru Mihai; Holban, Alina Maria

2014-09-01

Bacterial cellulose-silica hybrid composites were prepared starting from wet bacterial cellulose (BC) membranes using Stöber reaction. The structure and surface morphology of hybrid composites were examined by FTIR and SEM. The SEM pictures revealed that the silica particles are attached to BC fibrils and are well dispersed in the BC matrix. The influence of silica particles upon BC crystallinity was studied using XRD analysis. Thermogravimetric (TG) analysis showed that the composites are stable up to 300°C. A Plackett-Burman design was applied in order to investigate the influence of process parameters upon silica particle sizes and silica content of BC-silica composites. The statistical model predicted that it is possible for silica particles size to vary the synthesis parameters in order to obtain silica particles deposed on BC membranes in the range from 34.5 to 500 nm, the significant parameters being ammonia concentration, reaction time and temperature. The silica content also varies depending on process parameters, the statistical model predicting that the most influential parameters are water-tetraethoxysilane (TEOS) ratio and reaction temperature. The antimicrobial behavior on Staphylococcus aureus of BC-silica composites functionalized with usnic acid (UA) was also studied, in order to create improved surfaces with antiadherence and anti-biofilm properties. Copyright © 2014 Elsevier B.V. All rights reserved.

An AeroCom assessment of black carbon in Arctic snow and sea ice

DOE Office of Scientific and Technical Information (OSTI.GOV)

Jiao, C.; Flanner, M. G.; Balkanski, Y.

2014-01-01

Though many global aerosols models prognose surface deposition, only a few models have been used to directly simulate the radiative effect from black carbon (BC) deposition to snow and sea ice. In this paper, we apply aerosol deposition fields from 25 models contributing to two phases of the Aerosol Comparisons between Observations and Models (AeroCom) project to simulate and evaluate within-snow BC concentrations and radiative effect in the Arctic. We accomplish this by driving the offline land and sea ice components of the Community Earth System Model with different deposition fields and meteorological conditions from 2004 to 2009, during whichmore » an extensive field campaign of BC measurements in Arctic snow occurred. We find that models generally underestimate BC concentrations in snow in northern Russia and Norway, while overestimating BC amounts elsewhere in the Arctic. Although simulated BC distributions in snow are poorly correlated with measurements, mean values are reasonable. The multi-model mean (range) bias in BC concentrations, sampled over the same grid cells, snow depths, and months of measurements, are -4.4 (-13.2 to +10.7) ng g -1 for an earlier phase of AeroCom models (phase I), and +4.1 (-13.0 to +21.4) ng g -1 for a more recent phase of AeroCom models (phase II), compared to the observational mean of 19.2 ng g -1. Factors determining model BC concentrations in Arctic snow include Arctic BC emissions, transport of extra-Arctic aerosols, precipitation, deposition efficiency of aerosols within the Arctic, and meltwater removal of particles in snow. Sensitivity studies show that the model–measurement evaluation is only weakly affected by meltwater scavenging efficiency because most measurements were conducted in non-melting snow. The Arctic (60–90° N) atmospheric residence time for BC in phase II models ranges from 3.7 to 23.2 days, implying large inter-model variation in local BC deposition efficiency. Combined with the fact that most Arctic BC deposition originates from extra-Arctic emissions, these results suggest that aerosol removal processes are a leading source of variation in model performance. The multi-model mean (full range) of Arctic radiative effect from BC in snow is 0.15 (0.07–0.25) W m -2 and 0.18 (0.06–0.28) W m -2 in phase I and phase II models, respectively. After correcting for model biases relative to observed BC concentrations in different regions of the Arctic, we obtain a multi-model mean Arctic radiative effect of 0.17 W m -2 for the combined AeroCom ensembles. Finally, there is a high correlation between modeled BC concentrations sampled over the observational sites and the Arctic as a whole, indicating that the field campaign provided a reasonable sample of the Arctic.« less

DOE Office of Scientific and Technical Information (OSTI.GOV)

Kulkarni, S.; Sobhani, N.; Miller-Schulze, J. P.

Particulate matter (PM) mass concentrations, seasonal cycles, source sector, and source region contributions in Central Asia (CA) are analyzed for the period April 2008–July 2009 using the Sulfur Transport and dEposition Model (STEM) chemical transport model and modeled meteorology from the Weather Research and Forecasting (WRF) model. Predicted aerosol optical depth (AOD) values (annual mean value ~0.2) in CA vary seasonally, with lowest values in the winter. Surface PM 2.5 concentrations (annual mean value ~10 μg m −3) also exhibit a seasonal cycle, with peak values and largest variability in the spring/summer, and lowest values and variability in the wintermore » (hourly values from 2 to 90 μg m −3). Surface concentrations of black carbon (BC) (mean value ~0.1 μg m −3) show peak values in the winter. The simulated values are compared to surface measurements of AOD as well as PM 2.5, PM 10, BC, and organic carbon (OC) mass concentrations at two regional sites in Kyrgyzstan (Lidar Station Teplokluchenka (LST) and Bishkek). The predicted values of AOD and PM mass concentrations and their seasonal cycles are fairly well captured. The carbonaceous aerosols are underpredicted in winter, and analysis suggests that the winter heating emissions are underestimated in the current inventory. Dust, from sources within and outside CA, is a significant component of the PM mass and drives the seasonal cycles of PM and AOD. On an annual basis, the power and industrial sectors are found to be the most important contributors to the anthropogenic portion of PM 2.5. Residential combustion and transportation are shown to be the most important sectors for BC. Biomass burning within and outside the region also contributes to elevated PM and BC concentrations. The analysis of the transport pathways and the variations in particulate matter mass and composition in CA demonstrates that this region is strategically located to characterize regional and intercontinental transport of pollutants. Aerosols at these sites are shown to reflect dust, biomass burning, and anthropogenic sources from Europe; South, East, and Central Asia; and Russia depending on the time period. Simulations for a reference 2030 emission scenario based on pollution abatement measures already committed to in current legislation show that PM 2.5 and BC concentrations in the region increase, with BC growing more than PM 2.5 on a relative basis. This indicates that both the health impacts and the climate warming associated with these particles may increase over the next decades unless additional control measures are taken. The importance of observations in CA to help characterize the changes that are rapidly taking place in the region are discussed.« less

Simulation of Arctic Black Carbon using Hemispheric CMAQ: Role of Russia's BC Emissions, Transport, and Deposition

NASA Astrophysics Data System (ADS)

Huang, K.; Fu, J. S.

2015-12-01

Black carbon plays a unique role in the Arctic climate system due to its multiple effects. It causes Arctic warming by directly absorbing sunlight from space and by darkening the surface albedo of snow and ice, which indirectly leads to further warming and melting, thus inducing an Arctic amplification effect. BC depositions over the Arctic are more sensitive to regions in close proximity. In this study, we reconstruct BC emissions for Russian Federation, which is the country that occupies the largest area in the Arctic Circle. Local Russia information such as activity data, emission factors and other emission source data are used. In 2010, total anthropogenic BC emission of Russia is estimated to be around 254 Gg. Gas flaring, a commonly ignored black carbon source, contributes a dominant 43.9% of Russia's total anthropogenic BC emissions. Other sectors, i.e., residential, transportation, industry, and power plants, contribute 22.0%, 17.8%, 11.5%, and 4.8%, respectively. BC simulations were conducted using the hemispheric version of CMAQ with polar projection. Emission inputs are from a global emissions database EDGAR (Emissions Database for Global Atmospheric Research)-HTAPv2 (Hemispheric Transport of Air Pollution) and EDGAR-HTAPv2 with its Russian part replaced by the newly developed Russian BC emissions, respectively. The simulations using the new Russian BC emission inventory could improve 46 - 61% of the Absorption Aerosol Optical Depth (AAOD) measured at the AERONET sites in Russia throughout the whole year as compared to that using the default HTAPv2 emissions. At the four air monitoring sites (Zeppelin, Barrow, Alert, and Tiksi) in the Arctic Circle, surface BC simulations are improved the most during the Arctic haze periods (October - March). Emission perturbation studies show that Russia's BC emissions contribute over 50% of the surface BC concentrations over the Arctic during the cold seasons. This study demonstrates the good capability of H-CMAQ in simulating the transport of BC particles to the Arctic and suggests that the impact of Russian emissions on the Arctic haze has likely been underestimated, which is one of the causes that previous modeling works struggled in reproducing the BC levels in the Arctic region.

Ship-based Observations of Atmospheric Black Carbon Particles over the Arctic Ocean, Bering Sea, and North Western Pacific Ocean on 2016: Comparisons with Regional Chemical Transport Model simulations

NASA Astrophysics Data System (ADS)

Taketani, F.; Miyakawa, T.; Takigawa, M.; Yamaguchi, M.; Kanaya, Y.; Komazaki, Y.; Takashima, H.; Mordovskoi, P.; Tohjima, Y.

2017-12-01

Black carbon (BC), formed through the incomplete combustion of fossil fuels, biofuels, and biomass, is a major component of light-absorbing particulate matter in the atmosphere, causing positive radiative forcing. Also, BC deposition on the surface reduces the Earth's albedo and accelerates snow/ice melting by absorbing the sunlight. Therefore, the impact of BC on the Arctic climate needs to be assessed; however, observational information has been still insufficient. Over the Arctic Ocean, we have been conducting ship-based BC observations using a single particle soot photometer (SP2) on R/V Mirai every summer since 2014. To estimate the transport pathways of BC, we have also conducted model simulations during the period of cruise using a regional transport model (WRF-Chem 3.8.1). Here we focus on observations conducted on-board the R/V Mirai from 22 August to 5 October 2016 in a round trip to the Arctic Ocean through the Bering Strait from a port of Hachinohe (40.52N, 141.51E), Japan. We captured relatively high BC mass concentration events in this observation. The observed average BC mass concentration during 2016 was 0.8 ± 1.4 ng/m3 in >70N, similar to the levels ( 1.0ng/m3) recorded during our previous observations in the Arctic during 2014 and 2015. The variations in the observed concentrations in 2016 were qualitatively well reproduced by the regional chemical transport model. Quantitatively, however, the model tended to overestimate the BC levels, suggesting the possibilities that the emission rates were overestimated and/or the removal rates were underestimated. We will present further analysis on the size distribution, coating, and possible sources.

Climate Impacts of CALIPSO-Guided Corrections to Black Carbon Aerosol Vertical Distributions in a Global Climate Model

NASA Astrophysics Data System (ADS)

Kovilakam, Mahesh; Mahajan, Salil; Saravanan, R.; Chang, Ping

2017-10-01

We alleviate the bias in the tropospheric vertical distribution of black carbon aerosols (BC) in the Community Atmosphere Model (CAM4) using the Cloud-Aerosol and Infrared Pathfinder Satellite Observations (CALIPSO)-derived vertical profiles. A suite of sensitivity experiments are conducted with 1x, 5x, and 10x the present-day model estimated BC concentration climatology, with (corrected, CC) and without (uncorrected, UC) CALIPSO-corrected BC vertical distribution. The globally averaged top of the atmosphere radiative flux perturbation of CC experiments is ˜8-50% smaller compared to uncorrected (UC) BC experiments largely due to an increase in low-level clouds. The global average surface temperature increases, the global average precipitation decreases, and the ITCZ moves northward with the increase in BC radiative forcing, irrespective of the vertical distribution of BC. Further, tropical expansion metrics for the poleward extent of the Northern Hemisphere Hadley cell (HC) indicate that simulated HC expansion is not sensitive to existing model biases in BC vertical distribution.

Observed high-altitude warming and snow cover retreat over Tibet and the Himalayas enhanced by black carbon aerosols

DOE Office of Scientific and Technical Information (OSTI.GOV)

Xu, Y.; Ramanathan, V.; Washington, W. M.

Himalayan mountain glaciers and the snowpack over the Tibetan Plateau provide the headwater of several major rivers in Asia. In situ observations of snow cover extent since the 1960s suggest that the snowpack in the region have retreated significantly, accompanied by a surface warming of 2–2.5°C observed over the peak altitudes (5000 m). Using a high-resolution ocean–atmosphere global climate model and an observationally constrained black carbon (BC) aerosol forcing, we attribute the observed altitude dependence of the warming trends as well as the spatial pattern of reductions in snow depths and snow cover extent to various anthropogenic factors. At themore » Tibetan Plateau altitudes, the increase in atmospheric CO 2 concentration exerted a warming of 1.7°C, BC 1.3°C where as cooling aerosols cause about 0.7°C cooling, bringing the net simulated warming consistent with the anomalously large observed warming. We therefore conclude that BC together with CO 2 has contributed to the snow retreat trends. In particular, BC increase is the major factor in the strong elevation dependence of the observed surface warming. The atmospheric warming by BC as well as its surface darkening of snow is coupled with the positive snow albedo feedbacks to account for the disproportionately large role of BC in high-elevation regions. Here, these findings reveal that BC impact needs to be properly accounted for in future regional climate projections, in particular on high-altitude cryosphere.« less

Observed high-altitude warming and snow cover retreat over Tibet and the Himalayas enhanced by black carbon aerosols

DOE PAGES

Xu, Y.; Ramanathan, V.; Washington, W. M.

2016-02-05

Himalayan mountain glaciers and the snowpack over the Tibetan Plateau provide the headwater of several major rivers in Asia. In situ observations of snow cover extent since the 1960s suggest that the snowpack in the region have retreated significantly, accompanied by a surface warming of 2–2.5°C observed over the peak altitudes (5000 m). Using a high-resolution ocean–atmosphere global climate model and an observationally constrained black carbon (BC) aerosol forcing, we attribute the observed altitude dependence of the warming trends as well as the spatial pattern of reductions in snow depths and snow cover extent to various anthropogenic factors. At themore » Tibetan Plateau altitudes, the increase in atmospheric CO 2 concentration exerted a warming of 1.7°C, BC 1.3°C where as cooling aerosols cause about 0.7°C cooling, bringing the net simulated warming consistent with the anomalously large observed warming. We therefore conclude that BC together with CO 2 has contributed to the snow retreat trends. In particular, BC increase is the major factor in the strong elevation dependence of the observed surface warming. The atmospheric warming by BC as well as its surface darkening of snow is coupled with the positive snow albedo feedbacks to account for the disproportionately large role of BC in high-elevation regions. Here, these findings reveal that BC impact needs to be properly accounted for in future regional climate projections, in particular on high-altitude cryosphere.« less

Distribution and sources of dissolved black carbon in surface waters of the Chukchi Sea, Bering Sea, and the North Pacific Ocean

NASA Astrophysics Data System (ADS)

Nakane, Motohiro; Ajioka, Taku; Yamashita, Youhei

2017-05-01

Pyrogenic carbon, also called black carbon (BC), is an important component in the global carbon cycle. BC produced by biomass burning or fossil fuel combustion is transported to oceans by the atmosphere or rivers. However, environmental dynamics (i.e., major sources and sinks) of BC in marine environments have not been well documented. In this study, dissolved BC (DBC) collected from surface waters of the Chukchi Sea, the Bering Sea, and the subarctic and subtropical North Pacific were analyzed using the benzene polycarboxylic acid (BPCA) method. The DBC concentration and the ratio of B5CA and B6CA to all BPCAs (an index of the DBC condensation degree) ranged from 4.8 to 15.5 µg-C L-1 and from 0.20 to 0.43, respectively, in surface waters of the Chukchi/Bering Seas and the North Pacific Ocean. The concentration and condensation degree of DBC in the Chukchi/Bering Seas were higher and more variable than those in the subarctic and subtropical North Pacific, which implies that the major factors controlling DBC distribution were different in these marine provinces. In the Chukchi/Bering Seas, the DBC concentration was negatively correlated to salinity but positively correlated to chromophoric dissolved organic matter (CDOM) quantity and total dissolved lignin phenol concentration estimated by CDOM parameters. These correlations indicated that the possible major source of DBC in the Chukchi/Bering Seas was Arctic rivers. However, in the North Pacific, where riverine inputs are negligible for most sampling sites, DBC was possibly derived from the atmosphere. Although spectral slopes of CDOM at 275-295 nm (an index of the photodegradation degree of CDOM) differed widely between the subarctic and subtropical North Pacific, the concentration and condensation degrees of DBC were similar between the subarctic and subtropical North Pacific, which suggests that photodegradation was not the only major factor controlling DBC distribution. Therefore, DBC distributions of the North Pacific Ocean were considered to be mainly controlled by atmospheric deposition of BC and subsequent losses by photodegradation and adsorption onto sinking particles. This study implies that the main influence on DBC distribution in the open ocean and the coastal ocean are atmospheric deposition and fluvial inputs, respectively.

Temporal characteristics of black carbon concentrations and its potential emission sources in a southern Taiwan industrial urban area.

PubMed

Cheng, Yu-Hsiang; Lin, Chi-Chi; Liu, Jyh-Jian; Hsieh, Cheng-Ju

2014-03-01

This study investigates the temporal characteristics of black carbon and its potential emission sources, as well as the fractions of BC in PM2.5 levels in Kaohsiung urban area, which is an industrial city in southern Taiwan. Concentrations of BC and PM2.5 are monitored continuously from March 2006 to February 2010, using an aethalometer and a tapered element oscillating microbalance monitor. Additionally, the presence of organic compounds (or UV enhanced species) in particles at the sampling site is determined using the Delta-C (UVBC-BC) value. According to long-term measurement results, BC and PM2.5 concentrations are 3.33 and 34.0 μg m(-3), respectively, in the Kaohsiung urban area. The ratio of BC/PM2.5 is approximately 11 %. Low concentration of BC and PM2.5 in the summer of this study period is mostly likely owing to meteorological conditions that favored dispersion of local air pollutants. Nevertheless, BC concentrations peaked markedly during morning hours (7:00-11:00), likely owing to local traffic congestion. Measurement results suggest that BC is released from local traffic activities and emitted from industrial activities at this sampling site. Additionally, Delta-C values are significantly higher than zero during January-March and November-December periods in this industrial urban area, implying that UV enhanced species can be observed. At this sampling site, these UV enhanced species do not only originate from household activity and solid waste burning but also release from industrial activities. The elevated Delta-C values during nighttime (18:00-6:00) in the autumn and winter seasons are likely related to those UV enhanced species in the atmosphere, which can be condensed on particle surface under low temperature conditions. According to long-term measurement results, significantly positive Delta-C values can be observed under temperatures <20 °C and relative humidity of 60-75 % in this study. Despite the household activity and solid waste burning, the major sources of particles that are bound with UV enhanced species in this sampling site are industrial parks and a coal-fired power plant.

Vertical profiles and ground-based measurements of Black Carbon, Particulate matter and Optical properties over New Delhi during the foggy winters of 2015-16

NASA Astrophysics Data System (ADS)

Tiwari, S.; Bisht, D. S.; Srivastava, A. K.; Hopke, P. K.; Chakrabarty, R. K.

2016-12-01

Ground level and vertical observations of particulate matter were made as part of a pilot experiment using an air-quality monitory tethered balloon flown in the lower troposphere (1000 m) during the foggy winters of New Delhi, India. Measurements of black carbon (BC), the dominant absorber of visible light, particulate matter (PM), and the particulate optical properties along with meteorological parameters were conducted during the winter of 2015-16 in Delhi. During the study period, the mean concentrations of PM2.5, BC370nm, and BC880nm were observed to be 144.0 ± 39.7, 25.3 ± 8.5, and 19.4 ± 6.9 μg/m3, respectively. The mean value of PM2.5 is 12 times higher than the daily US-EPA air quality standard. The contribution of BC370nm in PM2.5 is 18 %. During the foggy period, the ground level concentrations of fine (PM2.5) and soot (BC370nm) particles increased substantially (59% and 26%, respectively) in comparison to clear days. Also, the aerosol light extinction coefficient (σext) was much higher (mean: 610 Mm-1) indicating that atmosphere was not transparent resulting in lower visibility. High concentrations of PM2.5 (89 µg/m3) and BC880nm (25.7 µg/m3) were observed up to 200 m (fog persists in this layer) in January. The BC880nm and PM2.5 concentrations near 1 km were significantly higher ( 1.9 and 12 µg/m3), respectively. Direct radiative forcing (DRF) due to BC was estimated at the top of the atmosphere (TOA), surface (SFC), and atmospheric (ATM) and its resultant forcing were - 46.2 Wm-2 at SFC indicates the cooling effect. However, a positive value ( 20.8 Wm-2) of BC DRF at TOA indicates the warming effect over the study region. The resultant ATM DRF due to BC was positive (67.0 Wm-2) indicating a net warming effect in the atmosphere. The contribution of fossil fuel climate forcing due to BC was 79% and 21% was due to burning of biomass/biofuels. The higher mean atmospheric heating rate (2.05 K day-1) by BC in the winter season would probably strengthen the temperature inversion leading to poor dispersion and affecting the formation of clouds. Based on this study, serious detrimental impacts of high concentrations of BC and PM (especially PM2.5) on regional climate are likely, thereby highlighting the need for immediate, stringent measures to improve the regional air quality in northern India.

Black Carbon and Sulfate Aerosols in the Arctic: Long-term Trends, Radiative Impacts, and Source Attributions

NASA Astrophysics Data System (ADS)

Wang, H.; Zhang, R.; Yang, Y.; Smith, S.; Rasch, P. J.

2017-12-01

The Arctic has warmed dramatically in recent decades. As one of the important short-lived climate forcers, aerosols affect the Arctic radiative budget directly by interfering radiation and indirectly by modifying clouds. Light-absorbing particles (e.g., black carbon) in snow/ice can reduce the surface albedo. The direct radiative impact of aerosols on the Arctic climate can be either warming or cooling, depending on their composition and location, which can further alter the poleward heat transport. Anthropogenic emissions, especially, BC and SO2, have changed drastically in low/mid-latitude source regions in the past few decades. Arctic surface observations at some locations show that BC and sulfate aerosols had a decreasing trend in the recent decades. In order to understand the impact of long-term emission changes on aerosols and their radiative effects, we use the Community Earth System Model (CESM) equipped with an explicit BC and sulfur source-tagging technique to quantify the source-receptor relationships and decadal trends of Arctic sulfate and BC and to identify variations in their atmospheric transport pathways from lower latitudes. The simulation was conducted for 36 years (1979-2014) with prescribed sea surface temperatures and sea ice concentrations. To minimize potential biases in modeled large-scale circulations, wind fields in the simulation are nudged toward an atmospheric reanalysis dataset, while atmospheric constituents including water vapor, clouds, and aerosols are allowed to evolve according to the model physics. Both anthropogenic and open fire emissions came from the newly released CMIP6 datasets, which show strong regional trends in BC and SO2 emissions during the simulation time period. Results show that emissions from East Asia and South Asia together have the largest contributions to Arctic sulfate and BC concentrations in the upper troposphere, which have an increasing trend. The strong decrease in emissions from Europe, Russia and North America contributed significantly to the overall decreasing trend in Arctic BC and sulfate, especially, in the lower troposphere. The long-term changes in the spatial distributions of aerosols, their radiative impacts and source attributions, along with implications for the Arctic warming trend, will be discussed.

Enhanced sorption of PAHs in natural-fire-impacted sediments from Oriole Lake, California.

PubMed

Sullivan, Julia; Bollinger, Kevyn; Caprio, Anthony; Cantwell, Mark; Appleby, Peter; King, John; Ligouis, Bertrand; Lohmann, Rainer

2011-04-01

Surface sediment cores from Oriole Lake (CA) were analyzed for organic carbon (OC), black carbon (BC), and their δ(13)C isotope ratios. Sediments displayed high OC (20-25%) and increasing BC concentrations from ∼0.40% (in 1800 C.E.) to ∼0.60% dry weight (in 2000 C.E.). Petrographic analysis confirmed the presence of fire-derived carbonaceous particles/BC at ∼2% of total OC. Natural fires were the most likely cause of both elevated polycyclic aromatic hydrocarbon (PAH) concentrations and enhanced sorption in Oriole Lake sediments prior to 1850, consistent with their tree-ring-based fire history. In contrast to other PAHs, retene and perylene displayed decreasing concentrations during periods with natural fires, questioning their use as fire tracers. The occurrence of natural fires, however, did not result in elevated concentrations of black carbon or chars in the sediments. Only the 1912-2007 sediment layer contained anthropogenic particles, such as soot BC. In this layer, combining OC absorption with adsorption to soot BC (using a Freundlich coefficient n = 0.7) explained the observed sorption well. In the older layers, n needed to be 0.3 and 0.5 to explain the enhanced sorption to the sediments, indicating the importance of natural chars/inertinites in sorbing PAHs. For phenanthrene, values of n differed significantly between sorption to natural chars (0.1-0.4) and sorption to anthropogenic black carbon (>0.5), suggesting it could serve as an in situ probe of sorbents.

Salivary carbonic anhydrase VI and its relation to salivary flow rate and buffer capacity in pregnant and non-pregnant women.

PubMed

Kivelä, Jyrki; Laine, Merja; Parkkila, Seppo; Rajaniemi, Hannu

2003-08-01

Previous studies have shown that pregnancy may have unfavourable effects on oral health. The pH and buffer capacity (BC) of paraffin-stimulated saliva, for example, have been found to decrease towards late pregnancy. Salivary carbonic anhydrase VI (CA VI) probably protects the teeth by accelerating the neutralization of hydrogen ions in the enamel pellicle on dental surfaces. Since estrogens and androgens are known to regulate CA expression in some tissues, we studied here whether salivary CA VI concentration shows pregnancy-related changes. Paraffin-stimulated salivary samples were collected from nine pregnant women 1 month before delivery and about 2 months afterwards and assayed for salivary CA VI concentration, BC and flow rate. The enzyme concentration was determined using a specific time-resolved immunofluorometric assay. The control group consisted of 17 healthy non-pregnant women. The results indicated that salivary CA VI levels varied markedly among individuals, but no significant differences in mean concentrations were seen between the samples collected during late pregnancy and postpartum. BC values were lower during pregnancy, however. Our findings suggest that CA VI secretion is not significantly affected by the hormonal alterations associated with pregnancy, and confirm the earlier reports that CA VI is not involved in the regulation of actual salivary BC.

Abiotic reduction of trifluralin and pendimethalin by sulfides in black-carbon-amended coastal sediments.

PubMed

Gong, Wenwen; Liu, Xinhui; Xia, Shuhua; Liang, Baocui; Zhang, Wei

2016-06-05

Dinitroaniline herbicides such as trifluralin and pendimethalin are persistent bioaccumulative toxins to aquatic organisms. Thus, in-situ remediation of contaminated sediments is desired. This study investigated whether black carbons (BCs), including apple wood charcoal (BC1), rice straw biochar (BC2), and activated carbon (BC3), could facilitate abiotic reduction of trifluralin and pendimethalin by sulfides of environmentally-relevant concentrations in anoxic coastal sediments. The reduction rates of trifluralin and pendimethalin increased substantially with increasing BC dosages in the sediments. This enhancing effect was dependent on BC type with the greatest for BC3 followed by BC1 and BC2, which well correlated with their specific surface area. The pseudo-first order reduction rate constants (kobs) for BC3-amended sediment (2%) were 13- and 14 times the rate constants in the BC-free sediment. The reduction rates increased with increasing temperature from 8 to 25°C in the BC-amended sediment, following the Arrhenius relationship. Finally, through molecular modeling by density functional theory and reaction species identification from mass spectra, molecular pathways of trifluralin and pendimethalin reduction were elucidated. In contrary to the separate sequential reduction of each nitro group to amine group, both nitro groups, first reduced to nitroso, then eventually to amine groups. Copyright © 2016 Elsevier B.V. All rights reserved.

Benzalkonium Chloride Provides Remarkable Stability to Liquid Protein Lures for Trapping Anastrepha obliqua (Diptera: Tephritidae).

PubMed

Lasa, R; Williams, T

2017-12-05

Hydrolyzed protein lures are widely used to monitor fruit fly pests but are rapidly degraded by microbial activity and must be replaced frequently. To improve the stability of lures, the quaternary ammonium biocide, benzalkonium chloride (BC), was evaluated in mixtures with two hydrolyzed proteins commonly used to monitor Anastrepha spp. The mean number of Anastrepha obliqua adults captured during six consecutive weeks using Captor + borax with the addition of 240 mg BC/liter, not renewed during the test, was similar to Captor + borax that was replaced at weekly intervals and was more effective than Captor + borax without BC. Numbers of A. obliqua flies captured in 30% CeraTrap diluted in water containing 240 mg BC/liter were similar to those caught in traps baited with Captor + borax or 30% CeraTrap without BC in the first 9 d of evaluation but was significantly more effective than both lures after 56 d. After >2 mo of use, 30% CeraTrap containing 240 mg BC/liter remained as effective as newly prepared 30% CeraTrap. The addition of BC to lures reduced surface tension of liquid lures by ~40-50%. However, when BC was increased to 720 mg BC/liter, only a small additional reduction in surface tension was observed and higher concentrations of BC did not increase capture rates. These findings could contribute to reduced costs for trapping networks and the development of long-lasting formulations of liquid protein lures for bait stations and mass-trapping targeted at major tephritid pests. © The Author(s) 2017. Published by Oxford University Press on behalf of Entomological Society of America. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Chemical, mechanical and biological properties of contemporary composite surface sealers.

PubMed

Anagnostou, Maria; Mountouris, George; Silikas, Nick; Kletsas, Dimitris; Eliades, George

2015-12-01

To evaluate the chemical, mechanical, and biological properties of modern composite surface sealers (CSS) having different compositions. The CSS products tested were Biscover LV (BC), Durafinish (DF), G-Coat Plus (GC), and Permaseal (PS). The tests performed were: (A): degree of conversion (DC%) by ATR-FTIR spectroscopy; (B): thickness of O2-inhibition layer by transmission optical microscopy; (C): surface hardness, 10 min after irradiation and following 1 week water storage, employing a Vickers indenter (VHN); (D): color (ΔE*) and gloss changes (ΔGU) after toothbrush abrasion, using L*a*b* colorimetry and glossimetry; (E): accelerated wear (GC,PS only) by an OHSU wear simulator plus 3D profilometric analysis, and (F): cytotoxicity testing of aqueous CSS eluents on human gingival fibroblast cultures employing the methyl-(3)H thymidine DNA labeling method. Statistical analyses included 1-way (A, B, ΔE*, ΔGU) and 2-way (C, F) ANOVAs, plus Tukey post hoc tests. Student's t-test was used to evaluate the results of the accelerated wear test (α=0.05 for all). The rankings of the statistical significant differences were: (A) PS (64.9)>DF,BC,GC (56.1-53.9) DC%; (B) DF,PS (12.3,9.8)>GC,BC (5.2,4.8) μm; (C): GC (37.6)>BC,DF (32.6,31.1)>PS (26.6) VHN (10 min/dry) and BC,DF (29.3,28.7)>GC(26.5)>PS(21.6) VHN (1w/water), with no significant material/storage condition interaction; (D): no differences were found among GC,DF,BC,PS (0.67-1.11) ΔE*, with all values within the visually acceptable range and PS,BC (32.8,29.4)>GC,DF (19.4,12.9) ΔGU; (E): no differences were found between GC and PS in volume loss (0.10,0.11 mm(3)), maximum (113.9,130.5 μm) and mean wear depths (30.3,27.5 μm); (F): at 1% v/v concentration, DF showed toxicity (23% vital cells vs 95-102% for others). However, at 5% v/v concentration DF (0%) and BC (9%) were the most toxic, whereas GC (58%) and PS (56%) showed moderate toxicity. Important chemical, mechanical, and biological properties exist among the CSS tested, which may affect their clinical performance. Copyright © 2015 Academy of Dental Materials. Published by Elsevier Ltd. All rights reserved.

Do contemporary (1980-2015) emissions determine the elemental carbon deposition trend at Holtedahlfonna glacier, Svalbard?

NASA Astrophysics Data System (ADS)

Ruppel, Meri M.; Soares, Joana; Gallet, Jean-Charles; Isaksson, Elisabeth; Martma, Tõnu; Svensson, Jonas; Kohler, Jack; Pedersen, Christina A.; Manninen, Sirkku; Korhola, Atte; Ström, Johan

2017-10-01

The climate impact of black carbon (BC) is notably amplified in the Arctic by its deposition, which causes albedo decrease and subsequent earlier snow and ice spring melt. To comprehensively assess the climate impact of BC in the Arctic, information on both atmospheric BC concentrations and deposition is essential. Currently, Arctic BC deposition data are very scarce, while atmospheric BC concentrations have been shown to generally decrease since the 1990s. However, a 300-year Svalbard ice core showed a distinct increase in EC (elemental carbon, proxy for BC) deposition from 1970 to 2004 contradicting atmospheric measurements and modelling studies. Here, our objective was to decipher whether this increase has continued in the 21st century and to investigate the drivers of the observed EC deposition trends. For this, a shallow firn core was collected from the same Svalbard glacier, and a regional-to-meso-scale chemical transport model (SILAM) was run from 1980 to 2015. The ice and firn core data indicate peaking EC deposition values at the end of the 1990s and lower values thereafter. The modelled BC deposition results generally support the observed glacier EC variations. However, the ice and firn core results clearly deviate from both measured and modelled atmospheric BC concentration trends, and the modelled BC deposition trend shows variations seemingly independent from BC emission or atmospheric BC concentration trends. Furthermore, according to the model ca. 99 % BC mass is wet-deposited at this Svalbard glacier, indicating that meteorological processes such as precipitation and scavenging efficiency have most likely a stronger influence on the BC deposition trend than BC emission or atmospheric concentration trends. BC emission source sectors contribute differently to the modelled atmospheric BC concentrations and BC deposition, which further supports our conclusion that different processes affect atmospheric BC concentration and deposition trends. Consequently, Arctic BC deposition trends should not directly be inferred based on atmospheric BC measurements, and more observational BC deposition data are required to assess the climate impact of BC in Arctic snow.

Characterization of Particulate Matter Profiling and Alveolar Deposition from Biomass Burning in Northern Thailand: The 7-SEAS Study

NASA Technical Reports Server (NTRS)

Chuang, Hsiao-Chi; Hsiao, Ta-Chih; Wang, Sheng-Hsiang; Tsay, Si-Chee; Lin, Neng-Huei

2016-01-01

Biomass burning (BB) frequently occurs in SouthEast Asia (SEA), which significantly affects the air quality and could consequently lead to adverse health effects. The aim of this study was to characterize particulate matter (PM) and black carbon (BC) emitted from BB source regions in SEA and their potential of deposition in the alveolar region of human lungs. A 31-day characterization of PM profiling was conducted at the Doi Ang Khang (DAK) meteorology station in northern Thailand in March 2013. Substantial numbers of PM (10147 +/- 5800 # per cubic centimeter) with a geometric mean diameter (GMD) of 114.4 +/- 9.2 nm were found at the study site. The PM of less than 2.5 micron in aerodynamic diameter (PM sub 2.5) hourly-average mass concentration was 78.0 +/- 34.5 per cubic microgram whereas the black carbon (BC) mass concentration was 4.4 +/- 2.6 micrograms per cubic meter. Notably, high concentrations of nanoparticle surface area (100.5 +/- 54.6 square micrometers per cubic centimeter) emitted from biomass burning can be inhaled into the human alveolar region. Significant correlations with fire counts within different ranges around DAK were found for particle number, the surface area concentration of alveolar deposition, and BC. In conclusion, biomass burning is an important PM source in SEA, particularly nanoparticles, which has high potency to be inhaled into the lung environment and interact with alveolar cells, leading to adverse respiratory effects. The fire counts within 100 to 150 km shows the highest Pearson's r for particle number and surface area concentration. It suggests 12 to 24 hr could be a fair time scale for initial aging process of BB aerosols. Importantly, the people lives in this region could have higher risk for PM exposure.

Sources and physicochemical characteristics of black carbon aerosol from the southeastern Tibetan Plateau: internal mixing enhances light absorption

NASA Astrophysics Data System (ADS)

Wang, Qiyuan; Cao, Junji; Han, Yongming; Tian, Jie; Zhu, Chongshu; Zhang, Yonggang; Zhang, Ningning; Shen, Zhenxing; Ni, Haiyan; Zhao, Shuyu; Wu, Jiarui

2018-04-01

Black carbon (BC) aerosol has important effects on the climate and hydrology of the Tibetan Plateau (TP). An intensive measurement campaign was conducted at Lulang (˜ 3300 m a.s.l. - above sea level), southeastern TP, from September to October 2015, to investigate the sources and physicochemical characteristics of refractory BC (rBC) aerosol. The average rBC mass concentration was 0.31 ± 0.55 µg m-3, which is higher than most prior results for BC on the TP. A clear diurnal cycle in rBC showed high values in the morning and low values in the afternoon. A bivariate polar plot showed that rBC loadings varied with wind speed and direction, which also reflected the dominant transport direction. The estimated net surface rBC transport intensity was +0.05 ± 0.29 µg s-1 m-2, indicating stronger transport from outside the TP compared with its interior. Cluster analysis and a concentration-weighted trajectory model connected emissions from north India to the high rBC loadings, but the effects of internal TP sources should not be overlooked. The average mass median diameter (MMD) of rBC was 160 ± 23 nm, with smaller MMDs on rainy days (145 nm) compared with non-rainy days (164 nm). The average number fraction of thickly coated rBC (FrBC) was 39 ± 8 %, and it increased with the O3 mixing ratios from 10:00 to 14:00 LT, indicating that photochemical oxidation played a role in forming rBC coatings. The average rBC absorption enhancement (Eabs) was estimated to be 1.9, suggesting that light absorption by coated rBC particles was greater than for uncoated ones. The Eabs was strongly positively correlated with the FrBC, indicating an amplification of light absorption for internally mixed rBC. For rBC cores < 170 nm, Eabs was negatively correlated with MMD, but it was nearly constant for rBC cores > 170 nm. Our study provides insight into the sources and evolution of rBC aerosol on the TP, and the results should be useful for improving models of the radiative effects of carbonaceous aerosols in this area.

Airborne black carbon concentrations over an urban region in western India-temporal variability, effects of meteorology, and source regions.

PubMed

Bapna, Mukund; Sunder Raman, Ramya; Ramachandran, S; Rajesh, T A

2013-03-01

This study characterizes over 5 years of high time resolution (5 min), airborne black carbon (BC) concentrations (July 2003 to December 2008) measured over Ahmedabad, an urban region in western India. The data were used to obtain different time averages of BC concentrations, and these averages were then used to assess the diurnal, seasonal, and annual variability of BC over the study region. Assessment of diurnal variations revealed a strong association between BC concentrations and vehicular traffic. Peaks in BC concentration were co-incident with the morning (0730 to 0830, LST) and late evening (1930 to 2030, LST) rush hour traffic. Additionally, diurnal variability in BC concentrations during major festivals (Diwali and Dushera during the months of October/November) revealed an increase in BC concentrations due to fireworks displays. Maximum half hourly BC concentrations during the festival days were as high as 79.8 μg m(-3). However, the high concentrations rapidly decayed suggesting that local meteorology during the festive season was favorable for aerosol dispersion. A multiple linear regression (MLR) model with BC as the dependent variable and meteorological parameters as independent variables was fitted. The variability in temperature, humidity, wind speed, and wind direction accounted for about 49% of the variability in measured BC concentrations. Conditional probability function (CPF) analysis was used to identify the geographical location of local source regions contributing to the effective BC measured (at 880 nm) at the receptor site. The east north-east (ENE) direction to the receptor was identified as a major source region. National highway (NH8) and two coal-fired thermal power stations (at Gandhinagar and Sabarmati) were located in the identified direction, suggesting that local traffic and power plant emissions were likely contributors to the measured BC.

Catchment-scale redistribution of lithogenic solutes and black carbon over three years following wildfire in the Jemez Mountains, New Mexico, USA

NASA Astrophysics Data System (ADS)

Pohlmann, M. A.; Root, R.; Abrell, L.; Schwartz, C. J.; Chorover, J.

2017-12-01

Wildfire represents a disturbance that is becoming more prevalent as climate shifts to hotter and drier conditions in the southwestern US. It has profound and potentially long-term effects on the physical, chemical and microbiological properties of soil, including immediate surface deposition of lithogenic elements and incompletely combusted organic matter (i.e., black carbon or BC) previously held in biomass. The long residence time of BC mitigates oxidative release of carbon to the atmosphere and thus has implications for long-term climate forcing. Immediately following the 2013 Thompson Ridge wildfire in the Jemez River Basin Critical Zone Observatory, we sampled 22 soil profiles across a zero order basin at finely resolved depth intervals to 40 cm. Samples were collected again 12 and 24 months following the fire to assess redistribution of solutes and BC in the two years following fire. Water extractable anions, cations and carbon were measured for each sample and maps were generated by geostatistical interpolation. Additionally, the benzene polycarboxylic acid (BPCA) molecular marker method was employed for a selection of samples to quantify and characterize the BC content of the existing soil organic carbon pool as a function of landscape position and time. The `pulsed' deposition of water-soluble ions and BC followed pre-fire vegetation structure as indicated by solution chemistry data for years one and two displaying elevated solute concentrations in surface depths proximal to dense vegetation. Vertical and lateral redistribution of the water extractable elements and BC were consistent with wetting front propagation and topographic trends (driven by erosion, overland flow and lateral subsurface flow). BC depth profiles indicate vertical infiltration and lateral transport with burial, the latter associated with surface erosion of sediment, as mechanisms for redistribution.

Insights into the binding behavior of bovine serum albumin to black carbon nanoparticles and induced cytotoxicity

NASA Astrophysics Data System (ADS)

Wu, Hai; Chen, Miaomiao; Shang, Mengting; Li, Xiang; Mu, Kui; Fan, Suhua; Jiang, Shuanglin; Li, Wenyong

2018-07-01

Black carbon (BC) is a main component of particulate matter (PM2.5). Due to their small size (<100 nm), inhaled ultrafine BC nanoparticles may penetrate the lung alveoli, where they interact with surfactant proteins and lipids, causing more serious damage to human health. Here, BC was analyzed to investigate the binding mechanism of its interaction with protein and induction of cytotoxicity changes. The binding process and protein conformation between BC and a serum protein (bovine serum albumin, BSA) were monitored by using a fluorescence quenching technique and UV-vis absorption, Fourier transform infrared (FTIR) and circular dichroism (CD) spectroscopies. The experimental results revealed that the fluorescence quenching of BSA induced by BC was a static quenching process and the hydrophobic force played the critical role in the interaction. The native conformation of BSA on the BC surface was slightly disturbed but obvious structural unfolding of the secondary structure did not occur. In the cytotoxicity study, BC nanoparticles with low concentrations exhibited strong toxicity towards BEAS-2B cells. However, the toxicity of BC nanoparticles could be mitigated by the presence of BSA. Therefore, proteins in biological fluids likely reduce the toxic effect of BC on human health. These findings delineated the binding mechanism and the toxicity between BC and the BSA-BC system, contributing to the understanding of the biological effects of BC exposure on human health in polluted atmospheres.

Climate Impacts of CALIPSO-Guided Corrections to Black Carbon Aerosol Vertical Distributions in a Global Climate Model

DOE Office of Scientific and Technical Information (OSTI.GOV)

Kovilakam, Mahesh; Mahajan, Salil; Saravanan, R.

Here, we alleviate the bias in the tropospheric vertical distribution of black carbon aerosols (BC) in the Community Atmosphere Model (CAM4) using the Cloud-Aerosol and Infrared Pathfinder Satellite Observations (CALIPSO)-derived vertical profiles. A suite of sensitivity experiments are conducted with 1x, 5x, and 10x the present-day model estimated BC concentration climatology, with (corrected, CC) and without (uncorrected, UC) CALIPSO-corrected BC vertical distribution. The globally averaged top of the atmosphere radiative flux perturbation of CC experiments is ~8–50% smaller compared to uncorrected (UC) BC experiments largely due to an increase in low-level clouds. The global average surface temperature increases, the globalmore » average precipitation decreases, and the ITCZ moves northward with the increase in BC radiative forcing, irrespective of the vertical distribution of BC. Further, tropical expansion metrics for the poleward extent of the Northern Hemisphere Hadley cell (HC) indicate that simulated HC expansion is not sensitive to existing model biases in BC vertical distribution.« less

Climate Impacts of CALIPSO-Guided Corrections to Black Carbon Aerosol Vertical Distributions in a Global Climate Model

DOE PAGES

Kovilakam, Mahesh; Mahajan, Salil; Saravanan, R.; ...

2017-09-13

Here, we alleviate the bias in the tropospheric vertical distribution of black carbon aerosols (BC) in the Community Atmosphere Model (CAM4) using the Cloud-Aerosol and Infrared Pathfinder Satellite Observations (CALIPSO)-derived vertical profiles. A suite of sensitivity experiments are conducted with 1x, 5x, and 10x the present-day model estimated BC concentration climatology, with (corrected, CC) and without (uncorrected, UC) CALIPSO-corrected BC vertical distribution. The globally averaged top of the atmosphere radiative flux perturbation of CC experiments is ~8–50% smaller compared to uncorrected (UC) BC experiments largely due to an increase in low-level clouds. The global average surface temperature increases, the globalmore » average precipitation decreases, and the ITCZ moves northward with the increase in BC radiative forcing, irrespective of the vertical distribution of BC. Further, tropical expansion metrics for the poleward extent of the Northern Hemisphere Hadley cell (HC) indicate that simulated HC expansion is not sensitive to existing model biases in BC vertical distribution.« less

Effect of Wegener-Bergeron-Findeisen Process to Black Carbon Simulation

NASA Astrophysics Data System (ADS)

Qi, Ling; Li, Qinbin; He, Cenlin; Wang, Xin; Huang, Jianping

2016-04-01

We systematically investigated the effect of Wegener-Bergeron-Findeisen (WBF) process to black carbon (BC) simulation by a global 3D chemical transport model GEOS-Chem constrained by measurements of BC scavenging efficiencies, concentration in air, deposition fluxes, concentration in snow and washout ratios. Including effect of WBF process reduces the annual mean BC scavenging efficiencies (the ratio of BC in cloud droplets to total BC) at all altitudes by 43-76% in the Arctic. For mid latitude BC scavenging efficiencies decrease by 8-22%, 23-39%, and 41-50% in lower (0-2 km), middle (2-5 km) and upper troposphere (5-10 km), respectively. Simulated BC in air in the Arctic and at mid altitude (˜4 km) in mid latitude increases by ˜40%, and the discrepancy reduces from -65% to -30%. Simulated median BC in snow decreases from 25.7 to 22.4 ng g-1, by 15% in mid latitude and increases from 8.7 to 11.0 ng g-1, by 26% in the Arctic and the comparison with observations improves. The model overestimates washout ratios (ratio of BC in fresh snow/rain to BC in surface air) at most of the sites by up to a factor of 165. With effect of WBF process included, the discrepancy decreases to a factor of 72. The simulated BC burden increases from 0.22 to 0.35 mg m-2 yr-1 when effect of WBF process is included, partly explains the scaled up of BC burden in Bond et al., 2013. Moreover, burden above 5 km increases from 22% to 27% when WBF process is included, indicating a higher forcing efficiency. We also found that BC simulation is insensitive to the temperature criteria between mixed phase clouds and ice clouds. The simulated BC burden is the same when the temperature is set as -15° C and -25° C. This study also suggests that more observations are needed to better distinguish riming dominated and WBF dominated conditions and better parameterize BC scavenging efficiency under the two conditions.

Chemical Composition and Sources of Aerosols in Finnish Arctic: 1964 - 2008

NASA Astrophysics Data System (ADS)

Husain, L.; Dutkiewicz, V. A.; Dejulio, A.; Ahmed, T.; Laing, J.; Hopke, P. K.; Paatero, J.; Viisanen, Y.

2013-12-01

BC particles strongly absorb solar radiation and impact the Earth's climate. In fact, BC may be the second largest contributor to global warming after greenhouses gases. However, the magnitude of the climate forcing by BC is quite uncertain, with a global average value estimated up to + 1.1W m-2 [Bond et al., 2013]. Direct long-term atmospheric measurements in the Arctic are required to evaluate the BC trends, variability and contributions from local as well as distant regional sources. Such information will permit the development of a strategy to minimize its impact on the climate. In this paper we report the measurements of concentrations of black carbon, [BC], SO4, methane sulfonic acid (MSA) and trace elements in filters collected weekly for 47 consecutive years at Kevo, Finland (69o 45' N and 27o 02' E) from 1964-2010. The data provides the longest record of direct measurement of these particulate species, and should be invaluable in assessing the impact of changes in emissions from nearby as well as distant sources. BC concentrations were determined in individual filters using thermal-optical and optical methods. The mean winter, spring, summer, and autumn [BC] were, 339, 199, 127, and 213 ngm-3, respectively. Annual [BC] decreased from 645 in 1965 to 82 ngm-3 in 2010, a nearly 8-fold decrease. There was a sharp decrease in concentrations after 1988, around the time of the collapse of the USSR. An overall decreasing trend was observed for all anthropogenic elements except lead where there was a decline that reflects the shift to unleaded gasoline. The 47-year complete data set will be analyzed by Positive Matrix Factorization (PMF). The receptor modeling results will be connected with back trajectory data in a Potential Source Contribution Function (PSCF) analysis to determine possible source areas. The combination of PMF and PSCF will identify sources and their geographic locations. Initial PSCF results with MSA show the Barents Sea and related areas as the source region while BC and sulfate come largely from Russia and Eastern Europe. The sulfate concentrations parallel the changes in estimated emission rates in Europe and Russia, but the BC concentration/emissions relationships are less clear. MSA has a weak but statistically significant correlation with the sea surface temperature anomaly within the areas identified by the PSCF analysis suggesting responses to temperature changes by the phytoplankton dimethyl sulfide emissions.

Characteristics and source apportionment of black carbon aerosols over an urban site.

PubMed

Rajesh, T A; Ramachandran, S

2017-03-01

Aethalometer based source apportionment model using the measured aerosol absorption coefficients at different wavelengths is used to apportion the contribution of fossil fuel and wood burning sources to the total black carbon (BC) mass concentration. Temporal and seasonal variabilities in BC mass concentrations, equivalent BC from fossil fuel (BC f f ), and wood burning (BC w b ) are investigated over an urban location in western India during January 2014 to December 2015. BC, BC f f , and BC w b mass concentrations exhibit strong diurnal variation and are mainly influenced by atmospheric dynamics. BC f f was higher by a factor of 2-4 than BC w b and contributes maximum to BC mass throughout the day, confirming consistent anthropogenic activities. Diurnal contribution of BC f f and BC w b exhibits opposite variation due to differences in emission sources over Ahmedabad. Night time BC values are about a factor of 1.4 higher than day time BC values. The annual mean percentage contributions of day time and night time are 42 and 58 %, respectively. BC, BC f f , and BC w b mass concentrations exhibit large and significant variations during morning, afternoon, evening, and night time. During afternoon, mass concentration values are minimum throughout the year because of the fully evolved boundary layer and reduced anthropogenic activities. BC exhibits a strong seasonal variability with postmonsoon high (8.3 μg m -3 ) and monsoon low (1.9 μg m -3 ). Annual mean BC f f and BC w b contributions are 80 and 20 %, respectively, to total BC, which suggests that major contribution of BC in Ahmedabad comes from fossil fuel emissions. The results show that the study location is dominated by fossil fuel combustion as compared to the emissions from wood burning. The results obtained represent a regional value over an urban regime which can be used as inputs on source apportionment to model BC emissions in regional and global climate models.

The Distribution of Snow Black Carbon observed in the Arctic and Compared to the GISS-PUCCINI Model

NASA Technical Reports Server (NTRS)

Dou, T.; Xiao, C.; Shindell, D. T.; Liu, J.; Eleftheriadis, K.; Ming, J.; Qin, D.

2012-01-01

In this study, we evaluate the ability of the latest NASA GISS composition-climate model, GISS-E2- PUCCINI, to simulate the spatial distribution of snow BC (sBC) in the Arctic relative to present-day observations. Radiative forcing due to BC deposition onto Arctic snow and sea ice is also estimated. Two sets of model simulations are analyzed, where meteorology is linearly relaxed towards National Centers for Environmental Prediction (NCEP) and towards NASA Modern Era Reanalysis for Research and Applications (MERRA) reanalyses. Results indicate that the modeled concentrations of sBC are comparable with presentday observations in and around the Arctic Ocean, except for apparent underestimation at a few sites in the Russian Arctic. That said, the model has some biases in its simulated spatial distribution of BC deposition to the Arctic. The simulations from the two model runs are roughly equal, indicating that discrepancies between model and observations come from other sources. Underestimation of biomass burning emissions in Northern Eurasia may be the main cause of the low biases in the Russian Arctic. Comparisons of modeled aerosol BC (aBC) with long-term surface observations at Barrow, Alert, Zeppelin and Nord stations show significant underestimation in winter and spring concentrations in the Arctic (most significant in Alaska), although the simulated seasonality of aBC has been greatly improved relative to earlier model versions. This is consistent with simulated biases in vertical profiles of aBC, with underestimation in the lower and middle troposphere but overestimation in the upper troposphere and lower stratosphere, suggesting that the wet removal processes in the current model may be too weak or that vertical transport is too rapid, although the simulated BC lifetime seems reasonable. The combination of observations and modeling provides a comprehensive distribution of sBC over the Arctic. On the basis of this distribution, we estimate the decrease in snow and sea ice albedo and the resulting radiative forcing. We suggest that the albedo reduction due to BC deposition presents significant space-time variations, with highest mean reductions of 1.25% in the Russian Arctic, which are much larger than those in other Arctic regions (0.39% to 0.64 %). The averaged value over the Arctic north of 66degN is 0.4-0.6% during spring, leading to regional surface radiative forcings of 0.7, 1.1 and 1.0Wm(exp-2) in spring 2007, 2008 and 2009, respectively.

Impacts of absorbing aerosol deposition on snowpack and hydrologic cycle in the Rocky Mountain region using variable-resolution CESM (VR-CESM)

NASA Astrophysics Data System (ADS)

Wu, C.; Liu, X.; Lin, Z.; Rahimi-Esfarjani, S. R.; Lu, Z.

2017-12-01

Deposition of light-absorbing aerosols (LAAs) including black carbon (BC) and dust onto snow surface has been suggested to reduce the snow albedo, and modulate the snowpack and consequent hydrologic cycle. In this study we use the variable-resolution Community Earth System Model (VR-CESM) to quantify the impacts of LAAs deposition onto snow in the Rocky Mountain region (RMR) during the period of 1981-2005. We first evaluate the model simulation of LAA concentrations both in the atmosphere and in snow, and then investigate the snowpack and runoff changes induced by LAAs-in-snow. The model simulates similar magnitudes of surface atmospheric dust concentrations as observations, but underestimates surface atmospheric BC concentrations by about a factor of two. Despite of this, the magnitude of BC-in-snow concentrations is overall comparable to observations. Regional mean surface radiative effect (SRE) due to LAAs-in-snow reaches up to 0.6-1.7 W m-2 in spring, and dust contributes to about 21-43% of total SRE. Maximum surface air temperature increase due to the LLA's SRE is around 0.9-1.1oC. Snow water equivalent and snow cover fraction reduce by around 2-50 mm and 0.05-0.2, respectively in the two regions around the mountains (Eastern Snake River Plain and Southwestern Wyoming) due to positive snow-albedo feedbacks. During the snow melting period, LAAs accelerate the hydrologic cycle with runoff increased by 7%-42% in April-May and reduced by 2-23% in June-July in the mountainous regions. Under the influence of LAAs-in-snow, Southern Rockies experience the most significant reduction of runoff by about 15% in the later stage of snow melt (i.e., June-July). Our results highlight the potentially important role of LAAs-in-snow in the historical and future changes of snowpack in the RMR.

Effects of black carbon and boundary layer interaction on surface ozone in Nanjing, China

NASA Astrophysics Data System (ADS)

Gao, Jinhui; Zhu, Bin; Xiao, Hui; Kang, Hanqing; Pan, Chen; Wang, Dongdong; Wang, Honglei

2018-05-01

As an important solar radiation absorbing aerosol, the effect of black carbon (BC) on surface ozone, via reducing photolysis rate, has been widely discussed by offline model studies. However, BC-boundary layer (BL) interactions also influence surface ozone. Using the online model simulations and process analysis, we demonstrate the significant impact of BC-BL interaction on surface ozone in Nanjing. The absorbing effect of BC heats the air above the BL and suppresses and delays the development of the BL, which eventually leads to a change in surface ozone via a change in the contributions from chemical and physical processes (photochemistry, vertical mixing and advection). For chemical processes, the suppression of the BL leads to large amounts of ozone precursors being confined below the BL which has an increased effect on ozone chemical production and offsets the decrease caused by the reduction of the photolysis rate, thus enhancing ozone chemical formation from 10:00 to 12:00 LT. Furthermore, changes in physical processes, especially the vertical mixing process, show a more significant influence on surface ozone. The weakened turbulence, caused by the suppressed BL, entrains much less ozone aloft down to the surface. Finally, summing-up the changes in the processes, surface ozone reduces before noon and the maximum reduction reaches 16.4 ppb at 12:00 LT. In the afternoon, the changes in chemical process are small which inconspicuously influence surface ozone. However, change in the vertical mixing process still influences surface ozone significantly. Due to the delayed development of the BL, there are obvious ozone gradients around the top of BL. Therefore, high concentrations of ozone aloft can still be entrained down to the surface which offsets the reduction of surface ozone. Comparing the changes in the processes, the change in vertical mixing plays the most important role in impacting surface ozone. Our results highlight the great impacts BC-BL interactions have on surface ozone by influencing the ozone contribution from physical process. This suggests that more attention should be paid to the mechanism of aerosol-BL interactions when controlling ozone pollution.

Black Carbon, Dust and Organic Matter at South Cascade Glacier in Washington State, USA: A Comprehensive Characterization of Temporal (1865-2014) and Spatial Variability

NASA Astrophysics Data System (ADS)

Kaspari, S.; Pittenger, D.; Swick, M.; Skiles, M.; Perez, A.; Sethi, H.; Sevier, E.

2017-12-01

Rising temperatures are a widely recognized cause of glacial retreat in Washington, however light absorbing aerosols (LAA, including black carbon (BC), dust and organic matter) can also contribute to increased melt by reducing snow albedo. We present updated results of BC and dust variability at South Cascade (SOCAS) glacier spanning 1865-1994 using a 158 m ice core. Peak BC deposition occurred between 1940-1958, when median BC concentrations were 25 times higher than background levels. Post 1958 BC concentrations decrease, followed by an increase post 1980 associated with melt consolidation and/or trans-Pacific aerosol transport. Dust deposition at SOCAS is dominated by local sources. Albedo reductions from LAA are dominated by dust deposition, except during high BC deposition events from wildfires, and during the 1940-1958 period when BC contributes equally to albedo reductions. Results from a 2014 field campaign that included collection of 3 shallow ice cores, surface snow, and snow albedo measurements allow the 1865-1994 ice core record to be extended toward present, and spatial variability in LAA to be characterized. Snow albedo transects were measured using a spectrometer. BC concentrations were measured using a Single Particle Soot Photometer (SP2). Gravimetric filtration was used to determine the total LAA, and a thermal gravimetric technique was used to partition the LAA between dust and organic matter. The organic matter was partitioned into organic and elemental carbon using a thermal optical method. These methods allow LAA abundances be measured, but to partition the contribution of the LAA to albedo reductions requires characterization of LAA optical properties. This was accomplished using a Hyperspectral Imaging Microscope Spectrometer method that allows particle reflectance to be measured at 138 nm2 pixel resolution. By combining these methods, we provide a comprehensive characterization of spatial and temporal LAA variability at SOCAS.

Association of marine viral and bacterial communities with reference black carbon particles under experimental conditions: an analysis with scanning electron, epifluorescence and confocal laser scanning microscopy.

PubMed

Cattaneo, Raffaela; Rouviere, Christian; Rassoulzadegan, Fereidoun; Weinbauer, Markus G

2010-11-01

Black carbon (BC), the product of incomplete combustion of fossil fuels and biomass, constitutes a significant fraction of the marine organic carbon pool. However, little is known about the possible interactions of BC and marine microorganisms. Here, we report the results of experiments using a standard reference BC material in high concentrations to investigate basic principles of the dynamics of natural bacterial and viral communities with BC particles. We assessed the attachment of viral and bacterial communities using scanning electron, epifluorescence and confocal laser scanning microscopy and shifts in bacterial community composition using 16S rRNA gene denaturing gradient gel electrophoresis (DGGE). In 24-h time-course experiments, BC particles showed a strong potential for absorbing viruses and bacteria. Total viral abundance was reduced, whereas total bacterial abundance was stimulated in the BC treatments. Viral and bacterial abundance on BC particles increased with particle size, whereas the abundances of BC-associated viruses and bacteria per square micrometer surface area decreased significantly with BC particle size. DGGE results suggested that BC has the potential to change bacterial community structure and favour phylotypes related to Glaciecola sp. Our study indicates that BC could influence processes mediated by bacteria and viruses in marine ecosystems. © 2010 Federation of European Microbiological Societies. Published by Blackwell Publishing Ltd. All rights reserved.

Historical record of black carbon in urban soils and its environmental implications.

PubMed

He, Yue; Zhang, Gan-Lin

2009-10-01

Energy use in urbanization has fundamentally changed the pattern and fluxes of carbon cycling, which has global and local environmental impacts. Here we have investigated organic carbon (OC) and black carbon (BC) in six soil profiles from two contrast zones in an ancient city (Nanjing) in China. BC in soils was widely variable, from 0.22 to 32.19 g kg(-1). Its average concentration in an ancient residential area (Zone 1) was, 0.91 g kg(-1), whereas in Zone 2, an industrial and commercial area, the figure was 8.62 g kg(-1). The ratio of BC/OC ranged from 0.06 to 1.29 in soil profiles, with an average of 0.29. The vertical distribution of BC in soil is suggested to reflect the history of BC formation from burning of biomass and/or fossil fuel. BC in the surface layer of soils was mainly from traffic emission (especially from diesel vehicles). In contrast, in cultural layers BC was formed from historical coal use. The contents of BC and the ratio of BC/OC may reflect different human activities and pollution sources in the contrasting urban zones. In addition, the significant correlation of heavy metals (Cu, Pb, and Zn) with BC contents in some culture layers suggests the sorption of the metals by BC or their coexistence resulted from the coal-involved smelting.

Global Air Quality and Health Co-benefits of Mitigating Near-term Climate Change Through Methane and Black Carbon Emission Controls

NASA Technical Reports Server (NTRS)

Anenberg, Susan C.; Schwartz, Joel; Shindell, Drew Todd; Amann, Markus; Faluvegi, Gregory S.; Klimont, Zbigniew; Janssens-Maenhout, Greet; Pozzoli, Luca; Dingenen, Rita Van; Vignati, Elisabetta;

Comprehensive Adsorption Studies of Doxycycline and Ciprofloxacin Antibiotics by Biochars Prepared at Different Temperatures

PubMed Central

Zeng, Zhi-wei; Tan, Xiao-fei; Liu, Yun-guo; Tian, Si-rong; Zeng, Guang-ming; Jiang, Lu-hua; Liu, Shao-bo; Li, Jiang; Liu, Ni; Yin, Zhi-hong

2018-01-01

This paper comparatively investigated the removal efficiency and mechanisms of rice straw biochars prepared under three pyrolytic temperatures for two kinds of tetracycline and quinolone antibiotics (doxycycline and ciprofloxacin). The influencing factors of antibiotic adsorption (including biochar dosage, pH, background electrolytes, humic acid, initial antibiotics concentration, contact time, and temperature) were comprehensively studied. The results suggest that biochars produced at high-temperature [i.e., 700°C (BC700)], have higher adsorption capacity for the two antibiotics than low-temperature (i.e., 300–500°C) biochars (BC300 and BC500). Higher surface area gives rise to greater volume of micropores and mesopores, and higher graphitic surfaces of the BC700 contributed to its higher functionality. The maximum adsorption capacity was found to be in the following order: DOX > CIP. The π-π EDA interaction and hydrogen bonding might be the predominant adsorption mechanisms. Findings in this study highlight the important roles of high-temperature biochars in controlling the contamination of tetracycline and quinolone antibiotics in the environment. PMID:29637067

Comprehensive adsorption studies of doxycycline and ciprofloxacin antibiotics by biochars prepared at different temperatures

NASA Astrophysics Data System (ADS)

Zeng, Zhi-wei; Tan, Xiao-fei; Liu, Yun-guo; Tian, Si-rong; Zeng, Guang-ming; Jiang, Lu-hua; Liu, Shao-bo; Li, Jiang; Liu, Ni; Yin, Zhi-hong

2018-03-01

This paper comparatively investigated the removal efficiency and mechanisms of rice straw biochars prepared under three pyrolytic temperatures for two kinds of tetracycline and quinolone antibiotics (doxycycline and ciprofloxacin). The influencing factors of antibiotic adsorption (including biochar dosage, pH, background electrolytes, humic acid, initial antibiotics concentration, contact time, and temperature) were comprehensively studied. The results suggest that biochars produced at high-temperature (i.e., 700°C (BC700)), have higher adsorption capacity for the two antibiotics than low-temperature (i.e., 300-500°C) biochars (BC300 and BC500). Higher surface area gives rise to greater volume of micropores and mesopores, and higher graphitic surfaces of the BC700 contributed to its higher functionality. The maximum adsorption capacity was found to be in the following order: DOX > CIP. The π-π EDA interaction and hydrogen bonding might be the predominant adsorption mechanisms. Findings in this study highlight the important roles of high-temperature biochars in controlling the contamination of tetracycline and quinolone antibiotics in the environment.

Diurnal cycling of urban aerosols under different weather regimes

NASA Astrophysics Data System (ADS)

Gregorič, Asta; Drinovec, Luka; Močnik, Griša; Remškar, Maja; Vaupotič, Janja; Stanič, Samo

2016-04-01

A one month measurement campaign was performed in summer 2014 in Ljubljana, the capital of Slovenia (population 280,000), aiming to study temporal and spatial distribution of urban aerosols and the mixing state of primary and secondary aerosols. Two background locations were chosen for this purpose, the first one in the city center (urban background - KIS) and the second one in the suburban background (Brezovica). Simultaneous measurements of black carbon (BC) and particle number size distribution of submicron aerosols (PM1) were conducted at both locations. In the summer season emission from traffic related sources is expected to be the main local contribution to BC concentration. Concentrations of aerosol species and gaseous pollutants within the planetary boundary layer are controlled by the balance between emission sources of primary aerosols and gases, production of secondary aerosols, chemical reactions of precursor gases under solar radiation and the rate of dilution by mixing within the planetary boundary layer (PBL) as well as with tropospheric air. Only local emission sources contribute to BC concentration during the stable PBL with low mixing layer height, whereas during the time of fully mixed PBL, regionally transported BC and other aerosols can contribute to the surface measurements. The study describes the diurnal behaviour of the submicron aerosol at the urban and suburban background location under different weather regimes. Particles in three size modes - nucleation (< 25 nm, NUM), Aitken (25 - 90 nm, AIM) and accumulation mode (90 - 800 nm, ACM), as well as BC mass concentration were evaluated separately for sunny, cloudy and rainy days, taking into account modelled values of PBL height. Higher particle number and black carbon concentrations were observed at the urban background (KIS) than at the suburban background location (Brezovica). Significant diurnal pattern of total particle concentration and black carbon concentration was observed at both locations, with a distinct morning and late afternoon peak. As a consequence of different PBL dynamics and atmospheric processes (photochemical effects, humidity, wind speed and direction), diurnal profile differs for sunny, cloudy and rainy days. Nucleation mode particles were found to be subjected to lower daily variation and only slightly influenced by weather, as opposed to Aitken and accumulation mode particles. The highest correlation between BC and particle number concentration is observed during stable atmospheric conditions in the night and morning hours and is attributed to different particle size modes, depending on the distance to local BC emission sources. In sunny weather conditions, correlation between BC and particle number concentration decreases during the day due to mixing in the atmosphere and formation of secondary aerosols. Black carbon aging and mixing with secondary aerosols was additionally studied on the aerosol samples taken from the morning to the evening of a sunny day using SEM-EDX technique.

Distribution and Sources of Black Carbon in the Arctic

NASA Astrophysics Data System (ADS)

Qi, Ling

The Arctic is warming at twice the global rate over recent decades. To slow down this warming trend, there is growing interest in reducing the impact from short-lived climate forcers, such as black carbon (BC), because the benefits of mitigation are seen more quickly relative to CO2 reduction. To propose efficient mitigation policies, it is imperative to improve our understanding of BC distribution in the Arctic and to identify the sources. In this dissertation, we investigate the sensitivity of BC in the Arctic, including BC concentrations in snow (BCsnow) and BC concentrations in air (BCair), to emissions, dry deposition and wet scavenging using a global 3-D chemical transport model (CTM) GEOS-Chem. By including flaring emissions, estimating dry deposition velocity using resistance-in-series method, and including Wegener-Bergeron-Findeisen (WBF) in wet scavenging, simulated BCsnow in the eight Arctic sub-regions agree with the observations within a factor of two, and simulated BCair fall within the uncertainty range of observations. Specifically, we find that natural gas flaring emissions in Western Extreme North of Russia (WENR) strongly enhance BCsnow (by up to ?50%) and BCair (by 20-32%) during snow season in the so-called 'Arctic front', but has negligible impact on BC in the free troposphere. The updated dry deposition velocity over snow and ice is much larger than those used in most of global CTMs and agrees better with observation. The resulting BCsnow changes marginally because of the offsetting of higher dry and lower wet deposition fluxes. In contrast, surface BCair decreases strongly due to the faster dry deposition (by 27-68%). WBF occurs when the environmental vapor pressure is in between the saturation vapor pressure of ice crystals and water drops in mixed-phase clouds. As a result, water drops evaporate and releases BC particles in them back into the interstitial air. In most CTMs, WBF is either missing or represented by a uniform and low BC scavenging efficiency. In this dissertation, we relate WBF with temperature and ice mass fraction based on long-term observations in mixed-phase clouds. We find that WBF reduces BC scavenging efficiency globally, with larger decrease at higher latitude and altitude (from 8% in the tropics to 76% in the Arctic). WBF slows down and reduces wet deposition of BC and leave more BC in the atmosphere. Higher BC air results in larger dry deposition. The resulting total deposition is lower in mid-latitudes (by 12-34%) and higher in the Arctic (2-29%). Globally, including WBF significantly reduces the discrepancy of BCsnow (by 50%), BCair (by 50%), and washout ratios (by a factor of two to four). The remaining discrepancies in these variables suggest that in-cloud removal is likely still excessive over land. In the last part, we identify sources of surface atmospheric BC in the Arctic in springtime, when radiative forcing is the largest due to the high insolation and surface albedo. We find a large contribution from Asian anthropogenic sources (40-43%) and open biomass burning emissions from forest fires in South Siberia (29-41%). Outside the Arctic front, BC is strongly enhanced by episodic, direct transport events from Asia and Siberia after 12 days of transport. In contrast, in the Arctic front, a large fraction of the Asian contribution is in the form of 'chronic' pollution on 1-2 month timescale. As such, it is likely that previous studies using 5- or 10-day trajectory analyses strongly underestimated the contribution from Asia to surface BC in the Arctic. Our results point toward an urgent need for better characterization of flaring emissions of BC (e.g. the emission factors, temporal and spatial distribution), extensive measurements of both the dry deposition of BC over snow and ice, and the scavenging efficiency of BC in mixed-phase clouds, particularly over Ocean. More measurements of 14C are needed to better understand sources of BC (fossil fuel combustion versus biomass burning) and to provide additional constrain on BC simulations.

Significant cooling effect on the surface due to soot particles over Brahmaputra River Valley region, India: An impact on regional climate.

PubMed

Tiwari, S; Kumar, R; Tunved, P; Singh, S; Panicker, A S

2016-08-15

Black carbon (BC) is an important atmospheric aerosol constituent that affects the climate by absorbing (directly) the sunlight and modifying cloud characteristics (indirectly). Here, we present first time yearlong measurements of BC and carbon monoxide (CO) from an urban location of Guwahati located in the Brahmaputra River valley (BRV) in the northeast region of India from 1st July 2013 to 30th June 2014. Daily BC concentrations varied within the range of 2.86 to 11.56μgm(-3) with an annual average of 7.17±1.89μgm(-3), while, CO varied from 0.19 to 1.20ppm with a mean value of 0.51±0.19ppm during the study period. The concentrations of BC (8.37μgm(-3)) and CO (0.67ppm) were ~39% and ~55% higher during the dry months (October to March) than the wet months (April to September) suggesting that seasonal changes in meteorology and emission sources play an important role in controlling these species. The seasonal ΔBC/ΔCO ratios were highest (lowest) in the pre-monsoon (winter) 18.1±1.4μgm(-3)ppmv(-1) (12.6±2.2μgm(-3)ppmv(-1)) which indicate the combustion of biofuel/biomass as well as direct emissions from fossil fuel during the pre-monsoon season. The annual BC emission was estimated to be 2.72Gg in and around Guwahati which is about 44% lower than the mega city 'Delhi' (4.86Gg). During the study period, the annual mean radiative forcing (RF) at the top of the atmosphere (TOA) for clear skies of BC was +9.5Wm(-2), however, the RF value at the surface (SFC) was -21.1Wm(-2) which indicates the net warming and cooling effects, respectively. The highest RF at SFC was in the month of April (-30Wm(-2)) which is coincident with the highest BC mass level. The BC atmospheric radiative forcing (ARF) was +30.16 (annual mean) Wm(-2) varying from +23.1 to +43.8Wm(-2). The annual mean atmospheric heating rate (AHR) due to the BC aerosols was 0.86Kday(-1) indicates the enhancement in radiation effect over the study region. The Weather Research and Forecasting model coupled with Chemistry (WRF-Chem) captured the seasonal cycle of observed BC fairly well but underestimated the observed BC during the month of May-August. Model results show that BC at Guwahati is controlled mainly by anthropogenic emissions except during the pre-monsoon season when open biomass burning also makes a similar contribution. Copyright © 2016 Elsevier B.V. All rights reserved.

Insights into the binding behavior of bovine serum albumin to black carbon nanoparticles and induced cytotoxicity.

PubMed

Wu, Hai; Chen, Miaomiao; Shang, Mengting; Li, Xiang; Mu, Kui; Fan, Suhua; Jiang, Shuanglin; Li, Wenyong

2018-07-05

Black carbon (BC) is a main component of particulate matter (PM 2.5 ). Due to their small size (<100nm), inhaled ultrafine BC nanoparticles may penetrate the lung alveoli, where they interact with surfactant proteins and lipids, causing more serious damage to human health. Here, BC was analyzed to investigate the binding mechanism of its interaction with protein and induction of cytotoxicity changes. The binding process and protein conformation between BC and a serum protein (bovine serum albumin, BSA) were monitored by using a fluorescence quenching technique and UV-vis absorption, Fourier transform infrared (FTIR) and circular dichroism (CD) spectroscopies. The experimental results revealed that the fluorescence quenching of BSA induced by BC was a static quenching process and the hydrophobic force played the critical role in the interaction. The native conformation of BSA on the BC surface was slightly disturbed but obvious structural unfolding of the secondary structure did not occur. In the cytotoxicity study, BC nanoparticles with low concentrations exhibited strong toxicity towards BEAS-2B cells. However, the toxicity of BC nanoparticles could be mitigated by the presence of BSA. Therefore, proteins in biological fluids likely reduce the toxic effect of BC on human health. These findings delineated the binding mechanism and the toxicity between BC and the BSA-BC system, contributing to the understanding of the biological effects of BC exposure on human health in polluted atmospheres. Copyright © 2018 Elsevier B.V. All rights reserved.

Variation of the radiative properties during black carbon aging: theoretical and experimental intercomparison

DOE PAGES

He, C.; Liou, K.-N.; Takano, Y.; ...

2015-07-20

A theoretical black carbon (BC) aging model is developed to account for three typical evolution stages, namely, freshly emitted aggregates, coated BC by soluble material, and BC particles undergoing further hygroscopic growth. The geometric-optics surface-wave (GOS) approach is employed to compute the BC single-scattering properties at each aging stage, which are subsequently compared with laboratory measurements. Theoretical calculations are consistent with measurements in extinction and absorption cross sections for fresh BC aggregates, but overestimate the scattering cross sections for BC mobility diameters of 155, 245, and 320 nm, because of uncertainties associated with theoretical calculations for small particles as wellmore » as laboratory scattering measurements. The measured optical cross sections for coated BC by sulfuric acid and for those undergoing further hygroscopic growth are captured by theoretical calculations using a concentric core-shell structure, with differences of less than 20 %. This suggests that the core-shell shape represents the realistic BC coating morphology reasonably well in this case, which is consistent with the observed strong structure compaction during aging. We find that the absorption and scattering properties of fresh BC aggregates vary by up to 60 % due to uncertainty in the BC refractive index, which, however, is a factor of two smaller in the case of coated BC particles. Sensitivity analyses on the BC morphology show that the optical properties of fresh BC aggregates are more sensitive to fractal dimension than primary spherule size. The absorption and scattering cross sections of coated BC particles vary by more than a factor of two due to different coating structures. We find an increase of 20–250 % in absorption and a factor of 3–15 in scattering during aging, significantly depending on coating morphology and aging stages. Applying the aging model to CalNex 2010 field measurements, we show that the resulting BC direct radiative forcing (DRF) first increases from 1.5 to 1.7 W m -2 and subsequently decreases to 1.0 W m -2 during the transport from the Los Angeles Basin to downwind regions, as a result of the competition between absorption enhancement due to coating and dilution of BC concentration. The BC DRF can vary by up to a factor of two due to differences in BC coating morphology. Thus, an accurate estimate of BC DRF requires the incorporation of a dynamic BC aging process that accounts for realistic morphology in climate models, particularly for the regional analysis with high atmospheric heterogeneity.« less

Variation of the radiative properties during black carbon aging: theoretical and experimental intercomparison

DOE Office of Scientific and Technical Information (OSTI.GOV)

He, C.; Liou, K.-N.; Takano, Y.

A theoretical black carbon (BC) aging model is developed to account for three typical evolution stages, namely, freshly emitted aggregates, coated BC by soluble material, and BC particles undergoing further hygroscopic growth. The geometric-optics surface-wave (GOS) approach is employed to compute the BC single-scattering properties at each aging stage, which are subsequently compared with laboratory measurements. Theoretical calculations are consistent with measurements in extinction and absorption cross sections for fresh BC aggregates, but overestimate the scattering cross sections for BC mobility diameters of 155, 245, and 320 nm, because of uncertainties associated with theoretical calculations for small particles as wellmore » as laboratory scattering measurements. The measured optical cross sections for coated BC by sulfuric acid and for those undergoing further hygroscopic growth are captured by theoretical calculations using a concentric core-shell structure, with differences of less than 20 %. This suggests that the core-shell shape represents the realistic BC coating morphology reasonably well in this case, which is consistent with the observed strong structure compaction during aging. We find that the absorption and scattering properties of fresh BC aggregates vary by up to 60 % due to uncertainty in the BC refractive index, which, however, is a factor of two smaller in the case of coated BC particles. Sensitivity analyses on the BC morphology show that the optical properties of fresh BC aggregates are more sensitive to fractal dimension than primary spherule size. The absorption and scattering cross sections of coated BC particles vary by more than a factor of two due to different coating structures. We find an increase of 20–250 % in absorption and a factor of 3–15 in scattering during aging, significantly depending on coating morphology and aging stages. Applying the aging model to CalNex 2010 field measurements, we show that the resulting BC direct radiative forcing (DRF) first increases from 1.5 to 1.7 W m -2 and subsequently decreases to 1.0 W m -2 during the transport from the Los Angeles Basin to downwind regions, as a result of the competition between absorption enhancement due to coating and dilution of BC concentration. The BC DRF can vary by up to a factor of two due to differences in BC coating morphology. Thus, an accurate estimate of BC DRF requires the incorporation of a dynamic BC aging process that accounts for realistic morphology in climate models, particularly for the regional analysis with high atmospheric heterogeneity.« less

Sediment Transport from Urban, Urbanizing, and Rural Areas in Johnson County, Kansas, 2006-08

USGS Publications Warehouse

Lee, Casey J.

2013-01-01

1. Studies have commonly illustrated that erosion and sediment transport from construction sites is extensive, typically 10-100X that of background levels. 2. However, to our knowledge, the affects of construction and urbanization have rarely been assessed (1) since erosion and sediment controls have been required at construction sites, and (2) at watershed (5-65 mi2) scales. This is primarily because of difficulty characterizing sediment loads in small basins. Studies (such as that illustrated from Timble, 1999) illustrated how large changes in surface erosion may not result in substantive changes in downstream sediment loads (b/c of sediment deposition on land-surfaces, floodplains, and in stream channels). 3. Improved technology (in-situ turbidity) sensors provide a good application b/c they provide an independent surrogate of sediment concentration that is more accurate at estimating sediment concentrations and loads that instantaneous streamflow.

Modelling Black Carbon concentrations in two busy street canyons in Brussels using CANSBC

NASA Astrophysics Data System (ADS)

Brasseur, O.; Declerck, P.; Heene, B.; Vanderstraeten, P.

2015-01-01

This paper focused on modelling Black Carbon (BC) concentrations in two busy street canyons, the Crown and Belliard Street in Brussels. The used original Operational Street Pollution Model was adapted to BC by eliminating the chemical module and is noted here as CANSBC. Model validations were performed using temporal BC data from the fixed measurement network in Brussels. Subsequently, BC emissions were adjusted so that simulated BC concentrations equalled the observed ones, averaged over the whole period of simulation. Direct validations were performed for the Crown Street, while BC model calculations for the Belliard Street were validated indirectly using the linear relationship between BC and NOx. Concerning the Crown Street, simulated and observed half-hourly BC concentrations correlated well (r = 0.74) for the period from July 1st, 2011 till June 30th, 2013. In particular, CANSBC performed very well to simulate the monthly and diurnal evolutions of averaged BC concentrations, as well as the difference between weekdays and weekends. This means that the model correctly handled the meteorological conditions as well as the variation in traffic emissions. Considering dispersion, it should however be noted that BC concentrations are better simulated under stable than under unstable conditions. Even if the correlation on half-hourly NOx concentrations was slightly lower (r = 0.60) than the one of BC, indirect validations of CANSBC for the Belliard Street yielded comparable results and conclusions as described above for the Crown Street. Based on our results, it can be stated that CANSBC is suitable to accurately simulate BC concentrations in the street canyons of Brussels, under the following conditions: (i) accurate vehicle counting data is available to correctly estimate traffic emissions, and (ii) vehicle speeds are measured in order to improve emission estimates and to take into account the impact of the turbulence generated by moving vehicles on the local dispersion of BC.

Biochar reduces copper toxicity in Chenopodium quinoa Willd. In a sandy soil.

PubMed

Buss, Wolfram; Kammann, Claudia; Koyro, Hans-Werner

2012-01-01

Mining, smelting, land applications of sewage sludge, the use of fungicides containing copper (Cu), and other human activities have led to widespread soil enrichment and contamination with Cu and potentially toxic conditions. Biochar (BC) can adsorb several substances, ranging from herbicides to plant-inhibiting allelochemicals. However, the range of potential beneficial effects on early-stage plant growth with regard to heavy metal toxicity is largely unexplored. We investigated the ameliorating properties of a forestry-residue BC under Cu toxicity conditions on early plant growth. Young quinoa plants () were grown in the greenhouse in the presence of 0, 2, and 4% BC application (w/w) added to a sandy soil with 0, 50, or 200 μg g Cu supplied. The plants without BC showed severe stress symptoms and reduced growth shortly after Cu application of 50 μg g and died at 200 μg Cu g. Increasing BC concentrations in the growth medium significantly increased the plant performance without Cu toxicity or under Cu stress. At the 4% BC application rate, the plants with 200 μg g Cu almost reached the same biomass as in the control treatment. In the presence of BC, less Cu entered the plant tissues, which had reduced Cu concentrations in the order roots, shoots, leaves. The amelioration effect also was reflected in the plant-soil system CO gas exchange, which showed clear signs of improvement with BC presence. The most likely ameliorating mechanisms were adsorption of Cu to negatively charged BC surfaces and an improvement of the water supply. Overall, BC seems to be a beneficial amendment with the potential to ameliorate Cu toxicity in sandy soils. Further research with a broad spectrum of different soil types, BCs, and crop plants is required. Copyright © by the American Society of Agronomy, Crop Science Society of America, and Soil Science Society of America, Inc.

Effects of humic acid and heavy metals on the sorption of polar and apolar organic pollutants onto biochars.

PubMed

Wang, Fei; Sun, Hongwen; Ren, Xinhao; Liu, Yarui; Zhu, Hongkai; Zhang, Peng; Ren, Chao

2017-12-01

The effects of humic acid (HA) and heavy metals (Cu 2+ and Ag + ) on the sorption of polar and apolar organic pollutants onto biochars that were produced at temperatures of 200 °C (BC200) and 700 °C (BC700) were studied. Due to the plentiful polar functional groups on BC200, cationic propranolol exhibited higher levels of sorption than naphthalene on BC200 while naphthalene and propranolol showed similar sorption capacities on BC700. HA changed the characteristics of biochars and generally inhibited the sorption of target organic pollutants on biochars; however, enhancement occurred in some cases depending on the pollutants involved and their concentrations, biochars used and the addition sequences and concentrations of HA. On BC200, HA modifications mainly influenced sorption by decreasing its polarity and increasing its aromaticity, while on BC700, the surface area and pore volume greatly decreased due to the pore-blocking effects of HA. Residue dissolved HA in solution may also contribute to sorption inhibition. Complexation between polar functional groups on BC200 and heavy metals slightly enhanced the sorption of neutral naphthalene and significantly enhanced that of anionic 4-nitro-1-naphtol, while limited the sorption of cationic propranolol. Heavy metals together with their associated water molecules decreased the sorption of target chemicals on BC700 via pore-filling or pore-mouth-covering. Inhibition of heavy metals for 4-nitro-1-naphthol was found to be the weakest due to the bridge effects of heavy metals between 4-nitro-1-naphtol and BC700. The higher polarizability of Ag + led to the increase of its sorption on biochars in the presence of organic aromatic pollutants. The results of the present study shed light on the sorption mechanisms of bi-solute systems and enable us to select suitable biochar sorbents when chemicals co-exist. Copyright © 2017. Published by Elsevier Ltd.

Quantifying sources, transport, deposition, and radiative forcing of black carbon over the Himalayas and Tibetan Plateau

DOE PAGES

Zhang, Rudong; Wang, Hailong; Qian, Yun; ...

2015-06-08

Black carbon (BC) particles over the Himalayas and Tibetan Plateau (HTP), both airborne and those deposited on snow, have been shown to affect snowmelt and glacier retreat. Since BC over the HTP may originate from a variety of geographical regions and emission sectors, it is essential to quantify the source–receptor relationships of BC in order to understand the contributions of natural and anthropogenic emissions and provide guidance for potential mitigation actions. In this study, we use the Community Atmosphere Model version 5 (CAM5) with a newly developed source-tagging technique, nudged towards the MERRA meteorological reanalysis, to characterize the fate ofmore » BC particles emitted from various geographical regions and sectors. Evaluated against observations over the HTP and surrounding regions, the model simulation shows a good agreement in the seasonal variation in the near-surface airborne BC concentrations, providing confidence to use this modeling framework for characterizing BC source–receptor relationships. Our analysis shows that the relative contributions from different geographical regions and source sectors depend on season and location in the HTP. The largest contribution to annual mean BC burden and surface deposition in the entire HTP region is from biofuel and biomass (BB) emissions in South Asia, followed by fossil fuel (FF) emissions from South Asia, then FF from East Asia. The same roles hold for all the seasonal means except for the summer, when East Asia FF becomes more important. For finer receptor regions of interest, South Asia BB and FF have the largest impact on BC in the Himalayas and central Tibetan Plateau, while East Asia FF and BB contribute the most to the northeast plateau in all seasons and southeast plateau in the summer. Central Asia and Middle East FF emissions have relatively more important contributions to BC reaching the northwest plateau, especially in the summer. Although local emissions only contribute about 10% of BC in the HTP, this contribution is extremely sensitive to local emission changes. Lastly, we show that the annual mean radiative forcing (0.42 W m -2) due to BC in snow outweighs the BC dimming effect (-0.3 W m -2) at the surface over the HTP. We also find strong seasonal and spatial variation with a peak value of 5 W m -2 in the spring over the northwest plateau. Such a large forcing of BC in snow is sufficient to cause earlier snow melting and potentially contribute to the acceleration of glacier retreat.« less

Quantifying sources, transport, deposition, and radiative forcing of black carbon over the Himalayas and Tibetan Plateau

DOE Office of Scientific and Technical Information (OSTI.GOV)

Zhang, Rudong; Wang, Hailong; Qian, Yun

Black carbon (BC) particles over the Himalayas and Tibetan Plateau (HTP), both airborne and those deposited on snow, have been shown to affect snowmelt and glacier retreat. Since BC over the HTP may originate from a variety of geographical regions and emission sectors, it is essential to quantify the source–receptor relationships of BC in order to understand the contributions of natural and anthropogenic emissions and provide guidance for potential mitigation actions. In this study, we use the Community Atmosphere Model version 5 (CAM5) with a newly developed source-tagging technique, nudged towards the MERRA meteorological reanalysis, to characterize the fate ofmore » BC particles emitted from various geographical regions and sectors. Evaluated against observations over the HTP and surrounding regions, the model simulation shows a good agreement in the seasonal variation in the near-surface airborne BC concentrations, providing confidence to use this modeling framework for characterizing BC source–receptor relationships. Our analysis shows that the relative contributions from different geographical regions and source sectors depend on season and location in the HTP. The largest contribution to annual mean BC burden and surface deposition in the entire HTP region is from biofuel and biomass (BB) emissions in South Asia, followed by fossil fuel (FF) emissions from South Asia, then FF from East Asia. The same roles hold for all the seasonal means except for the summer, when East Asia FF becomes more important. For finer receptor regions of interest, South Asia BB and FF have the largest impact on BC in the Himalayas and central Tibetan Plateau, while East Asia FF and BB contribute the most to the northeast plateau in all seasons and southeast plateau in the summer. Central Asia and Middle East FF emissions have relatively more important contributions to BC reaching the northwest plateau, especially in the summer. Although local emissions only contribute about 10% of BC in the HTP, this contribution is extremely sensitive to local emission changes. Lastly, we show that the annual mean radiative forcing (0.42 W m -2) due to BC in snow outweighs the BC dimming effect (-0.3 W m -2) at the surface over the HTP. We also find strong seasonal and spatial variation with a peak value of 5 W m -2 in the spring over the northwest plateau. Such a large forcing of BC in snow is sufficient to cause earlier snow melting and potentially contribute to the acceleration of glacier retreat.« less

The Importance of Asia as a Source of Black Carbon to the Arctic Constrained by Aircraft and Surface Measurements.

NASA Astrophysics Data System (ADS)

Xu, J.; Martin, R.; Morrow, A.; Sharma, S.; Huang, L.; Leaitch, W. R.; Burkart, J.; Schulz, H.; Zanatta, M.; Willis, M. D.; Henze, D. K.; Lee, C. J.; Herber, A. B.; Abbatt, J.

2017-12-01

The contribution of Asian sources to Arctic black carbon (BC) remains uncertain. We interpret a series of recent airborne (NETCARE 2015, PAMARCMiP 2009 and 2011 campaigns) and ground-based measurements (at Alert, Barrow and Ny-Ålesund) from multiple methods (thermal, laser incandescence and light absorption) with the GEOS-Chem global chemical transport model and its adjoint to attribute the sources of Arctic BC. Our simulations with the addition of seasonally varying domestic heating and of gas flaring emissions are consistent with ground-based measurements of BC concentrations at Alert and Barrow to within 13% in winter and spring, and with airborne measurements to within 17 % except for an underestimation in the middle troposphere (500-700 hPa). Sensitivity simulations suggest that anthropogenic emissions from eastern and southern Asia have the largest impact on the Arctic BC column burden both in spring (56 %) and annually (37 %), with the largest contribution in the middle troposphere (400-700 hPa). Anthropogenic emissions from northern Asia are the primary source of the Arctic surface BC ( 40% annually). Our adjoint simulations indicate noteworthy contributions from emissions in eastern China (15 %) and western Siberia (6.5 %) to the Arctic BC loadings on an annual average. Emissions from as south as the Indo-Gangetic Plain have a substantial impact (6.3 % annually) on Arctic BC as well. The Tarim oilfield in western China stands out as the second most influential grid cell with an annual contribution of 2.6 %. Gas flaring emissions from oilfields in western Siberia have a striking impact (13 %) on Arctic BC loadings in January, comparable to the total influence of continental Europe and North America (6.5 % each in January).

The Role of Trans Tensional Structures and Lake Mead Reservoir in Groundwater Flow in Black Canyon, Lake Mead National Recreation Area, NV-AZ

NASA Astrophysics Data System (ADS)

Justet, L.; Beard, S.

2010-12-01

Hot springs and seeps discharging into Black Canyon (BC) along the Colorado River in north Colorado River Valley (CRV) support endemic riparian ecosystems in the Lake Mead National Recreation Area. Increases in groundwater development in southern NV and northwestern AZ may impact spring discharge. Sources of spring discharge in BC were evaluated using geochemical methods. Kinematic analysis and geologic mapping of structures associated with BC springs were used to evaluate structural controls on groundwater flow in BC. Geochemical analysis indicates groundwater discharge near Hoover Dam (HD) and along the faulted edge of the Boulder City Pluton is derived from Lake Mead, high δ87Sr Proterozoic or Tertiary crystalline rock and, possibly, Tertiary sedimentary rock. Reducing conditions indicated by 234U/238U and δ34S concentrations suggest the groundwater is confined and/or derived from greater depths while carbon isotopes indicate the groundwater is old. Lighter δD and δO-18, modern tritium concentrations, post-Dam U disequilibrium ages, and occurrence of anthropogenic perchlorate support the presence of a young Lake Mead component. South of the pluton, the Lake Mead component is absent. More oxidizing conditions in this part of BC, indicated by the U and S isotope concentrations, suggest the groundwater is less confined and/or derived from shallower depths compared to groundwater discharging near HD. Older apparent groundwater ages and heavier δD and δO-18 values south of the pluton indicate slower flow paths from a lower elevation or latitude source. Clarifying the nature of groundwater flow in eastern NV, the analyses indicate that hydraulic connection between the regional carbonate aquifer and BC is unlikely. Instead, the data indicate sources of BC springs are derived relatively locally in CRV and, possibly, south Lake Mead Valley. Results of the geologic and kinematic analyses indicate faults that formed from the interaction of E-W extension related to the AZ extensional corridor and NW-SE trans tension related to the Lake Mead shear zone are the main controls on groundwater flow in the vicinity of HD and Boulder City Pluton. Most groundwater in BC appears to discharge along the NW-striking Palm Tree fault that parallels the northern edge of the pluton. Supported by trends in chemistry, an alignment of similar-elevation springs along a N-S striking fault that extends the length of west BC may be a flow path for groundwater from north BC to south of the pluton. South of the pluton, dikes intrude many of the faults and appear to act as flow barriers. Groundwater in this part of BC may flow through stacked layers of brecciated volcanic rock prevalent in the area. Flow from laterally adjacent valleys into BC would have to cross a N-S structural fabric that is not favored kinematically. Existing information implies an overall absence of significant surface discharge in BC prior to construction of HD. This indicates that the head created by impoundment of the Colorado River has likely pushed old, slow moving groundwater through CRV and, possibly, south Lake Mead Valley, to the surface in BC where it discharges as springs and seeps.

The Ascension Island boundary layer in the remote southeast Atlantic is often smoky

DOE PAGES

Zuidema, Paquita; Sedlacek III, Arthur J.; Flynn, Connor; ...

2018-03-31

Observations from June through October, 2016, from a surface-based ARM Mobile Facility deployment on Ascension Island (8°S, 14.5°W) indicate that refractory black carbon (rBC) is almost always present within the boundary layer. rBC mass concentrations, light absorption coefficients, and cloud condensation nuclei concentrations vary in concert and synoptically, peaking in August. Light absorption coefficients at three visible wavelengths as a function of rBC mass indirectly indicate the presence of other light-absorbing aerosols (e.g., brown carbon), most pronounced in June. The single-scattering-albedo increases systematically from August to October in both 2016 and 2017, with monthly-means of 0.78±0.02 (August), 0.81±0.03 (September) andmore » 0.83±0.03 (October) at the green wavelength. Boundary-layer aerosol loadings are only loosely correlated with total aerosol optical depth, with smoke more likely to be present in the boundary layer earlier in the biomass-burning season, evolving to smoke predominantly present above the cloud layers in September-October, typically resting upon the cloud-top inversion. The time period with the campaign-maximum near-surface light absorption and column aerosol optical depth, on 13-16 August of 2016, is investigated further. Also, backtrajectories indicate more direct boundary layer transport westward from the African continent is central to explaining the elevated surface aerosol loadings.« less

The Ascension Island boundary layer in the remote southeast Atlantic is often smoky

DOE Office of Scientific and Technical Information (OSTI.GOV)

Zuidema, Paquita; Sedlacek III, Arthur J.; Flynn, Connor

Observations from June through October, 2016, from a surface-based ARM Mobile Facility deployment on Ascension Island (8°S, 14.5°W) indicate that refractory black carbon (rBC) is almost always present within the boundary layer. rBC mass concentrations, light absorption coefficients, and cloud condensation nuclei concentrations vary in concert and synoptically, peaking in August. Light absorption coefficients at three visible wavelengths as a function of rBC mass indirectly indicate the presence of other light-absorbing aerosols (e.g., brown carbon), most pronounced in June. The single-scattering-albedo increases systematically from August to October in both 2016 and 2017, with monthly-means of 0.78±0.02 (August), 0.81±0.03 (September) andmore » 0.83±0.03 (October) at the green wavelength. Boundary-layer aerosol loadings are only loosely correlated with total aerosol optical depth, with smoke more likely to be present in the boundary layer earlier in the biomass-burning season, evolving to smoke predominantly present above the cloud layers in September-October, typically resting upon the cloud-top inversion. The time period with the campaign-maximum near-surface light absorption and column aerosol optical depth, on 13-16 August of 2016, is investigated further. Also, backtrajectories indicate more direct boundary layer transport westward from the African continent is central to explaining the elevated surface aerosol loadings.« less

In vitro cytotoxicity of calcium silicate-containing endodontic sealers.

PubMed

Zhou, Hui-min; Du, Tian-feng; Shen, Ya; Wang, Zhe-jun; Zheng, Yu-feng; Haapasalo, Markus

2015-01-01

The cytotoxicity of 2 novel calcium silicate-containing endodontic sealers to human gingival fibroblasts was studied. EndoSequence BC (Brasseler, Savannah, GA), MTA Fillapex (Angelus Indústria de Produtos Odontológicos S/A, Londrina, PR, Brazil) and a control sealer (AH Plus; Dentsply DeTrey GmbH, Konstanz, Germany) were evaluated. Human gingival fibroblasts were incubated for 3 days both with the extracts from fresh and set materials in culture medium and cultured on the surface of the set materials in Dulbecco-modified Eagle medium. Fibroblasts cultured in Dulbecco-modified Eagle medium were used as a control group. Cytotoxicity was evaluated by flow cytometry, and the adhesion of the fibroblasts to the surface of the set materials was assessed using scanning electron microscopy. The data of cell cytotoxicity were analyzed statistically using a 1-way analysis of variance test at a significance level of P < .05. Cells incubated with extracts from BC Sealer showed higher viabilities at all extract concentrations than cells incubated with extracts from freshly mixed AH Plus and fresh and set MTA Fillapex, esspecially for the high extract concentrations (1:2 and 1:8 dilutions). Extracts from set MTA Fillapex of 2 weeks and older were more cytotoxic than extracts from freshly mixed and 1-week-old cement. With extract concentrations of 1:32 and lower, MTA Fillapex was no longer cytotoxic. After setting, AH Plus was no longer cytotoxic, and the fibroblast cells grew on set AH Plus equally as well as on BC Sealer. BC Sealer and MTA Fillapex, the 2 calcium silicate-containing endodontic sealers, exhibited different cytotoxicity to human gingival fibroblasts. Copyright © 2015 American Association of Endodontists. Published by Elsevier Inc. All rights reserved.

Impact of pollutant emission reductions on summertime aerosol feedbacks: A case study over the PO valley

NASA Astrophysics Data System (ADS)

Carnevale, C.; Finzi, G.; Pederzoli, A.; Turrini, E.; Volta, M.; Ferrari, F.; Gianfreda, R.; Maffeis, G.

2015-12-01

This study presents an evaluation of the impact by future pollutant anthropogenic emission reductions on summertime aerosol feedbacks over the Po valley. The fully coupled on line model Wrf/Chem has been used to examine the air quality and meteorology response over the region to 2020 emission reductions with respect to a simulation base case (2013). Future changes in net short wave radiation flux (SW) are also analyzed. The model domain is a 6 × 6 km2 resolution grid over Northern Italy; the simulation period covers two summer months (July-August). The work is divided into two parts. In the first, model results for the Base Case simulation (BC) are evaluated by comparing Wrf/Chem output to surface observations provided by two monitoring networks. Approximately 25 sites belonging to the regional ARPA Lombardia Network are used for both chemistry (NO2, O3 and PM10 concentrations) and meteorology (wind speed and 2-meters temperature) evaluation; 4 stations part of the global AEROsol Robotic Network (AERONET) are used for the evaluation of Aerosol Optical Depth (AOD). In the second part, a Maximum Feasible Reduction (MFR) scenario at 2020 have been simulated for the same months; monthly direct, indirect and overall aerosols feedbacks for both BC and MFR have been computed and analyzed. The emission reductions in the MFR 2020 lead to a sensible change in the aerosol overall feedbacks for all variables; a drop of SW over the valley (cooling effect) is visible in both BC and MFR, but it is less significant in the MFR (-5 W m-2) compared to the BC (-45 W m-2). This difference is mainly due to the abatement of SO2 primary emissions, which leads to lower sulfates concentrations scattering radiation, thus mitigates the cooling effect and favors the warming. As SW is higher in the MFR, T2 also increases over land with respect to the BC (the cooling of -0.5 °C estimated in the Base Case almost disappears). The overall effects lead to an enhancement of PM10 concentration in the BC; they are less efficient in the MFR because of lower secondary aerosol concentrations (associated to the reduction of primary PM10 emissions by approximately 20%). Concerning NO2, some localized areas with high reductions in the BC are not visible in the MFR. This is consistent with the increase of T2, which leads to higher photolytic rates compared to the BC. Higher concentrations of NO2 in the MFR with respect to the BC lead to lower O3 concentrations (maximum O3 values drop from +6 ppb to +3 ppb).

Seasonal variations of sulfate, carbonaceous species (black carbon and polycyclic aromatic hydrocarbons), and trace elements in fine atmospheric aerosols collected at subtropical islands in the East China Sea

NASA Astrophysics Data System (ADS)

Kaneyasu, Naoki; Takada, Hideshige

2004-03-01

In order to characterize the outflow of pollution derived aerosols from the Asian Pacific rim to the North Pacific Ocean, seasonal variations of fine aerosol components (aerodynamic diameter <2 μm) were collected at two islands (Amami Island and Miyako Island) that surround the East China Sea. Monthly averaged concentrations of non-sea-salt SO42- (nss.SO42-) and black carbon (BC) at Amami and Miyako showed relatively high values in winter to spring and low values in summer. The observed seasonal variation is basically determined by the northwesterly monsoon in winter to spring and southeasterly wind from the stationary North Pacific anticyclone in summer. The minimum concentration levels of nss.SO42- and BC in summer were almost 2-3 times that of the North Pacific background level. Trace metals in aerosols showed similar seasonal variations observed for nss.SO42- and BC. The concentrations of nss.SO42- and Sb were highly correlated; this is in contradiction with the results at stations established in Pacific Exploratory Mission-West ground monitoring sites. Polycyclic aromatic hydrocarbons (PAHs) also showed a pronounced maximum in winter and/or spring, with maximum concentrations comparable in magnitude to those in spring at Barrow, Alaska. Many of the low molecular weight species of PAHs had high correlation with BC, suggesting that they were either transported independently in a similar way or were transported attached to BC. Furthermore, the relative abundance of some PAH species in the present study and those found in deep-ocean surface sediments sampled in the middle Pacific Ocean are compared and discussed.

Measurement of Atmospheric Black Carbon Concentrations, [BC]atm, in the Arctic Region from ~1700 to 2013

NASA Astrophysics Data System (ADS)

Husain, L.; Sarkar, S.; Jyethi, D. S.; Ruppel, M.; Dutkiewicz, V. A.

2015-12-01

Atmospheric black carbon (BC) aerosols play a key role in Earth's climate through direct and indirect effects. Due to a lack of long-term BC data, climate models are used to estimate BC based on fuel inventories, which have large uncertainties. Hence, long term BC data is needed to verify global models. We report here the first measurements of atmospheric BC concentrations, [BC]atm, from ~1700 to 2013 using sediments from Finnish lakes, Saanajarvi (SJ)(690 44' N, 200 52' E), and Vuoskojarvi (VJ)(69044'N, 26057'E). The cores were collected from the deepest parts of the lakes using a HTH gravity corer, sliced in 0.25 cm sections; freeze dried, and ages determined using 210Pb dating method. The BC was chemically separated, and [BC] determined by the thermal optical method. The [BC] varied from 50 to 1140µg/gdry weight in SJ; and 20 to 130µg/gdry weight in VJ. Husain et al.,(JGR, vol 113, D13102,doi:10.1029/2007JD009398, 2008) showed that the atmospheric deposition of BC into lake sediments depends on the characteristic of individual lakes, BC washout ratios, precipitation intensity, and sedimentation rates. The deposition rate, K, for a lake is defined by, [BC]sed = K[BC]atm where [BC]sed, is the concentration of BC in the sediment. We have measured [BC]atm from 1970 to 2010 in Kevo, Finland, where VJ and SJ are located. The [BC]atm from Kevo, and [BC]sed from VJ, and SJ were used to determine K for each of the lake. Owing to the availability of the long term atmospheric BC data from 1970 to 2010 multiple measurements of K were made, and provided a high measure of precision. The mean values of K for VJ, and SJ were 226 ± 60, and 830 ± 290 (m3air/ gdry weight). The K values were used to determine [BC]atm for the years before 1970. The [BC]atm from 2013 to 2006 was 82ng/m3. It increased slowly reaching a peak value of about 947 ± 322 ng/m3.The concentrations decreased subsequently to 244 ± 83ng/m3 in 1920, and changed little ~ 1774.The lowest concentration, 77 ± 26 ng/m3, was observed ~ 1700. The high atmospheric concentrations beyond 1850, perhaps, suggest a proportionally larger component from wood burning for heating. We plan to estimate [BC]atm using OsloCTM3 model, and inventory of fossil fuel, and biomass burning, and compare it with our measurements.

Temporal variations of black carbon during haze and non-haze days in Beijing

PubMed Central

Liu, Qingyang; Ma, Tangming; Olson, Michael R; Liu, Yanju; Zhang, Tingting; Wu, Yu; Schauer, James J.

2016-01-01

Black carbon (BC) aerosol has been identified as one of key factors responsible for air quality in Beijing. BC emissions abatement could help slow regional climate change while providing benefits for public health. In order to quantify its variations and contribution to air pollution, we systematically studied real-time measurements of equivalent black carbon (eBC) in PM2.5 aerosols at an urban site in Beijing from 2010 to 2014. Equivalent black carbon (eBC) is used instead of black carbon (BC) for data derived from Aethalometer-31 measurement. Equivalent BC concentrations showed significant temporal variations with seasonal mean concentration varying between 2.13 and 5.97 μg m−3. The highest concentrations of eBC were found during autumn and winter, and the lowest concentrations occurred in spring. We assessed the temporal variations of eBC concentration during haze days versus non-haze days and found significantly lower eBC fractions in PM2.5 on haze days compared to those on non-haze days. Finally, we observed a clear inverse relationship between eBC and wind speed. Our results show that wind disperses PM2.5 more efficiently than eBC; so, secondary aerosols are not formed to the same degree as primary aerosols over the same transport distance during windy conditions. PMID:27634102

Effect of the Agricultural Biomass Burning on the Ambient Air Quality of Lumbini

NASA Astrophysics Data System (ADS)

Mehra, M.; Panday, A. K.; Praveen, P. S.; Bhujel, A.; Pokhrel, S.; Ram, K.

2017-12-01

The emissions from increasing anthropogenic activities has led to degradation in ambient air quality of Lumbini (UNESCO world heritage site) and its surrounding environments. The presence of high concentrations of air pollutants is of concern because of its implications for public health, atmospheric visibility, chemistry, crop yield, weather and climate on a local to regional scale. The study region experiences wide-spread on-field agricultural residue burning, particularly in the months of November (paddy residue burning) and April (wheat residue burning). In an attempt to study the impact of emissions from post-harvest burning of paddy and wheat residue in Nepal, the International Centre for Integrated Mountain Development, in collaboration with the Government of Nepal's Department of Environment and the Lumbini International Research Institute, established the Lumbini Air Quality Observatory (LAQO) in May 2016 for continuous measurement of Black carbon (BC), particulate matter (PM10, PM2.5 & PM1), as well as concentration of gaseous pollutant and meteorological parameters. Here we present results of the surface observations from LAQO for the months with intensified paddy and wheat open biomass burning during November 2016 and April 2017, respectively. The average concentrations of BC, PM2.5 and PM10 were 11.3±6.2 µg m-3, 96.7±48.9 µg m-3 and 132.3±59.1 µg m-3 respectively during the month of November 2016. On the other hand, the surface concentrations of BC, PM2.5 and PM10 were found to be 11.0±8.3 µg m-3, 45.0±35.0 µg m-3 and 114.0±96.1 µg m-3 during April 2017. A significant increase in the primary pollutant concentration was observed during both types of open agricultural burning periods. However, BC/PM2.5 ratio was almost higher by factor of two during paddy burning as compared to wheat residue burning. Source characteristics and the relative contribution of agricultural burning to PM concentrations at Lumbini are being computed based on measurements of chemical tracers in ambient aerosol samples and these results will be discussed during the conference.

Re-evaluating black carbon in the Himalayas and the Tibetan Plateau: concentrations and deposition

NASA Astrophysics Data System (ADS)

Li, Chaoliu; Yan, Fangping; Kang, Shichang; Chen, Pengfei; Han, Xiaowen; Hu, Zhaofu; Zhang, Guoshuai; Hong, Ye; Gao, Shaopeng; Qu, Bin; Zhu, Zhejing; Li, Jiwei; Chen, Bing; Sillanpää, Mika

2017-10-01

Black carbon (BC) is the second most important warming component in the atmosphere after CO2. The BC in the Himalayas and the Tibetan Plateau (HTP) has influenced the Indian monsoon and accelerated the retreat of glaciers, resulting in serious consequences for billions of Asian residents. Although a number of related studies have been conducted in this region, the BC concentrations and deposition rates remain poorly constrained. Because of the presence of arid environments and the potential influence of carbonates in mineral dust (MD), the reported BC concentrations in the HTP are overestimated. In addition, large discrepancies have been reported among the BC deposition derived from lake cores, ice cores, snow pits and models. Therefore, the actual BC concentration and deposition values in this sensitive region must be determined. A comparison between the BC concentrations in acid (HCl)-treated and untreated total suspected particle samples from the HTP showed that the BC concentrations previously reported for the Nam Co station (central part of the HTP) and the Everest station (northern slope of the central Himalayas) were overestimated by approximately 52 ± 35 and 39 ± 24 %, respectively, because of the influence of carbonates in MD. Additionally, the organic carbon (OC) levels were overestimated by approximately 22 ± 10 and 22 ± 12 % for the same reason. Based on previously reported values from the study region, we propose that the actual BC concentrations at the Nam Co and Everest stations are 61 and 154 ng m-3, respectively. Furthermore, a comprehensive comparison of the BC deposition rates obtained via different methods indicated that the deposition of BC in HTP lake cores was mainly related to river sediment transport from the lake basin as a result of climate change (e.g., increases in temperature and precipitation) and that relatively little BC deposition occurred via atmospheric deposition. Therefore, previously reported BC deposition rates from lake cores overestimated the atmospheric deposition of BC in the HTP. Correspondingly, BC deposition derived from snow pits and ice cores agreed well with that derived from models, implying that the BC depositions of these two methods reflect the actual values in the HTP. Therefore, based on reported values from snow pits and ice cores, we propose that the BC deposition in the HTP is 17. 9 ± 5. 3 mg m-2 a-1, with higher and lower values appearing along the fringes and central areas of the HTP, respectively. These adjusted BC concentrations and deposition values in the HTP are critical for performing accurate evaluations of other BC factors, such as atmospheric distribution, radiative forcing and chemical transport in the HTP.

Effects of wet deposition on the abundance and size distribution of black carbon in East Asia

NASA Astrophysics Data System (ADS)

Kondo, Y.; Moteki, N.; Oshima, N.; Ohata, S.; Koike, M.; Shibano, Y.; Takegawa, N.; Kita, K.

2016-05-01

An improved understanding of the variations in the mass concentration and size distribution of black carbon (BC) in the free troposphere (FT) over East Asia, where BC emissions are very high, is needed to reliably estimate the radiative forcing of BC in climate models. We measured these parameters and the carbon monoxide (CO) concentration by conducting the Aerosol Radiative Forcing in East Asia (A-FORCE) 2013W aircraft campaign in East Asia in winter 2013 and compared these data with measurements made in the same region in spring 2009. The median BC concentrations in the FT originating from North China (NC) and South China (SC) showed different seasonal variations, which were primarily caused by variations in meteorological conditions. CO concentrations above the background were much higher in SC than in NC in both seasons, suggesting a more active upward transport of CO. In SC, precipitation greatly increased from winter to spring, leading to an increased wet deposition of BC. As a result, the median BC concentration in the FT was highest in SC air in winter. This season and region were optimal for the effective transport of BC from the planetary boundary layer to the FT. The count median diameters of the BC size distributions generally decreased with altitude via wet removal during upward transport. The altitude dependence of the BC size distributions was similar in winter and spring, in accord with the similarity in the BC mixing state. The observed BC concentrations and microphysical properties will be useful for evaluating the performance of climate models.

Arginine functionalized bacterial cellulose nanofibers containing gel as an effective wound dressing; in vitro and in vivo evaluation.

PubMed

Feizabadi, Farideh; Minaiyan, Mohsan; Taheri, Azade

2018-02-19

Nanofibers such as bacterial cellulose nanofibers (BC-NFs) have gained increasing attention for use in wound dressings. Topical application of arginine can stimulate wound healing significantly. In order to promote the wound healing process, arginine functionalized BC-NFs containing gel (Arg-BC-NFs gel) was prepared by the electrostatic attachment of arginine on the surface of BC-NFs. The effect of pH was evaluated on the amount of the attached arginine on the BC-NFs surface. The attachment of arginine on BC-NFs surface was investigated by FTIR spectroscopy. The morphology of Arg-BC-NFs was evaluated using FESEM. The viscosity and spreadability of Arg-BC-NFs and the release of arginine from Arg-BC-NFs were evaluated. The effectiveness of Arg-BC-NFs gel was assessed in a full thickness wound model in rats. Re-epithelization, collagen deposition and neovascularization were investigated in the wound tissues using histological and immunohistochemical analysis. FTIR spectra and the zeta potential of BC-NFs confirmed the surface modification of BC-NFs by arginine. FESEM images showed the nanofibrous structure of Arg-BC-NFs. The release of arginine from Arg-BC-NFs gel was in a sustained release manner for 24 h. The appropriate viscosity and spreadability of Arg-BC-NFs gel confirmed its easy topical application. In vivo studies revealed that Arg-BC-NFs gel promoted wound closure at a faster rate than BC-NFs gel and arginine solution. Moreover, faster and more organized re-epithelialization, angiogenesis and collagen deposition were achieved in Arg-BC-NFs gel treated group in comparison to other groups. Arg-BC-NFs gel can be introduced as an effective wound dressing for acute wounds. Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.org.

In Situ Observations of Snow Metamorphosis Acceleration Induced by Dust and Black Carbon

NASA Astrophysics Data System (ADS)

Schneider, A. M.; Flanner, M.

2017-12-01

Previous studies demonstrate the dependence of shortwave infrared (SWIR) reflectance on snow specific surface area (SSA) and others examine the direct darkening effect dust and black carbon (BC) deposition has on snow and ice-covered surfaces. The extent to which these light absorbing aerosols (LAAs) accelerate snow metamorphosis, however, is challenging to assess in situ as measurement techniques easily disturb snowpack. Here, we use two Near-Infrared Emitting Reflectance Domes (NERDs) to measure 1300 and 1550nm bidirectional reflectance factors (BRFs) of natural snow and experimental plots with added dust and BC. We obtain NERD measurements and subsequently collect and transport snow samples to the nearby U.S. Army Corps of Engineers' Cold Regions Research and Engineering Lab for micro computed tomography (micro-CT) analysis. Snow 1300 (1550) nm BRFs evolve from 0.6 (0.15) in fresh snow to 0.2 (0.03) after metamorphosis. Hourly-scale time evolving snow surface BRFs and SSA estimates from micro-CT reveal more rapid SWIR darkening and snow metamorphosis in contaminated versus natural plots. Cloudiness and high wind speeds can completely obscure these results if LAAs mobilize before absorbing enough radiant energy. These findings verify experimentally that dust and BC deposition can accelerate snow metamorphosis and enhance snow albedo feedback in sunny, calm weather conditions. Although quantifying the enhancement of snow albedo feedback induced by LAAs requires further surface temperature, solar irradiance, and impurity concentration measurements, this study provides experimental verification of positive feedback occurring where dust and BC accelerate snow metamorphosis.

The Ascension Island Boundary Layer in the Remote Southeast Atlantic is Often Smoky

DOE Office of Scientific and Technical Information (OSTI.GOV)

Zuidema, Paquita; Sedlacek, Arthur J.; Flynn, Connor

Observations from June through October, 2016, from a surface-based ARM Mobile Facility deployment on Ascension Island (8°S, 14.5°W) indicate that refractory black carbon (rBC) is almost always present within the boundary layer. rBC mass concentrations, light absorption coefficients, and cloud condensation nuclei concentrations vary in concert and synoptically, peaking in August. Derived mass absorption cross-sections using light absorptioin coefficients at three wavelengths as a function of rBC mass indirectly indicate the presence of other light-absorbing organic aerosols (e.g., brown carbon), most pronounced in June. A filter-based estimate of single-scattering-albedo increases systematically from August to October, also apparent in 2017. Boundary-layermore » aerosol loadings are only loosely correlated with total aerosol optical depth, with smoke more likely to be present in the boundary layer earlier in the biomass-burning season, evolving to smoke predominantly present in the free-troposphere in September-October, typically resting upon the cloud-top inversion. The time period with the campaign-maximum near-surface light absorption and column aerosol optical depth, on 13-16 August of 2016, is investigated further. Back trajectories indicate the boundary layer transport was directly westward from the African continent, which is unusual in August.« less

Variation of the radiative properties during black carbon aging: theoretical and experimental intercomparison

DOE PAGES

He, C.; Liou, K.-N.; Takano, Y.; ...

2015-10-28

A theoretical black carbon (BC) aging model is developed to account for three typical evolution stages, namely, freshly emitted aggregates, BC coated by soluble material, and BC particles undergoing further hygroscopic growth. The geometric-optics surface-wave (GOS) approach is employed to compute the BC single-scattering properties at each aging stage, which are subsequently compared with laboratory measurements. Theoretical calculations are consistent with measurements in extinction and absorption cross sections for fresh BC aggregates with different BC sizes (i.e., mobility diameters of 155, 245, and 320 nm), with differences of ≤ 25 %. The measured optical cross sections for BC coated bymore » sulfuric acid and for that undergoing further hygroscopic growth are generally captured (differences < 30 %) by theoretical calculations using a concentric core-shell structure, with an overestimate in extinction and absorption of the smallest BC size and an underestimate in scattering of the largest BC size. We find that the absorption and scattering cross sections of fresh BC aggregates vary by 20–40 and 50–65 %, respectively, due to the use of upper (1.95–0.79 i) and lower (1.75–0.63 i) bounds of BC refractive index, while the variations are < 20 % in absorption and < 50 % in scattering in the case of coated BC particles. Sensitivity analyses of the BC morphology show that the optical properties of fresh BC aggregates are more sensitive to fractal dimension than primary spherule size. The absorption and scattering cross sections of coated BC particles vary by more than a factor of 2 due to different coating structures. We find an increase of 20–250 % in absorption and a factor of 3–15 in scattering during aging, significantly depending on coating morphology and aging stages. This study suggests that an accurate estimate of BC radiative effects requires the incorporation of a dynamic BC aging process that accounts for realistic coating structures in climate models.« less

Variation of the radiative properties during black carbon aging: theoretical and experimental intercomparison

DOE Office of Scientific and Technical Information (OSTI.GOV)

He, C.; Liou, K.-N.; Takano, Y.

A theoretical black carbon (BC) aging model is developed to account for three typical evolution stages, namely, freshly emitted aggregates, BC coated by soluble material, and BC particles undergoing further hygroscopic growth. The geometric-optics surface-wave (GOS) approach is employed to compute the BC single-scattering properties at each aging stage, which are subsequently compared with laboratory measurements. Theoretical calculations are consistent with measurements in extinction and absorption cross sections for fresh BC aggregates with different BC sizes (i.e., mobility diameters of 155, 245, and 320 nm), with differences of ≤ 25 %. The measured optical cross sections for BC coated bymore » sulfuric acid and for that undergoing further hygroscopic growth are generally captured (differences < 30 %) by theoretical calculations using a concentric core-shell structure, with an overestimate in extinction and absorption of the smallest BC size and an underestimate in scattering of the largest BC size. We find that the absorption and scattering cross sections of fresh BC aggregates vary by 20–40 and 50–65 %, respectively, due to the use of upper (1.95–0.79 i) and lower (1.75–0.63 i) bounds of BC refractive index, while the variations are < 20 % in absorption and < 50 % in scattering in the case of coated BC particles. Sensitivity analyses of the BC morphology show that the optical properties of fresh BC aggregates are more sensitive to fractal dimension than primary spherule size. The absorption and scattering cross sections of coated BC particles vary by more than a factor of 2 due to different coating structures. We find an increase of 20–250 % in absorption and a factor of 3–15 in scattering during aging, significantly depending on coating morphology and aging stages. This study suggests that an accurate estimate of BC radiative effects requires the incorporation of a dynamic BC aging process that accounts for realistic coating structures in climate models.« less

Distribution, input pathway and mass inventory of black carbon in sediments of the Gulf of Thailand, SE Asia

NASA Astrophysics Data System (ADS)

Hu, Limin; Shi, Xuefa; Bai, Yazhi; Fang, Yin; Chen, Yingjun; Qiao, Shuqing; Liu, Shengfa; Yang, Gang; Kornkanitnan, Narumol; Khokiattiwong, Somkiat

2016-03-01

The coastal margins around Southeast Asia (SE Asia) may serve as an ideal location to study the source-sink process of sedimentary black carbon (BC) because SE Asia has been identified as one of the major BC emission source regions in the world. This study provides an extensive picture of recent regional-scale sedimentary BC sequestration in the Gulf of Thailand (GOT), a tropical marine system in SE Asia. Generally, the sedimentary BC concentrations (0.07-3.99 mg/g) were in the low to moderate ranges of those obtained in other coastal sediments around the world. Regional variability of the BC and its correlation with the sediment grain size and total organic carbon (TOC) content indicated a general hydrodynamic constraint on BC occurrence in the lower Gulf in contrast to the upper Gulf with a more source dependence due to the direct land-based input. BC/TOC% values and the varied BC components (char and soot), as well as their correlations suggested that char was the predominant constituents of sedimentary BC both in the upper and lower Gulf, which could be mainly derived from biomass burning and entered into the nearshore region through direct fluvial transport and surface run-off. The estimated BC burial flux (∼212 μg/cm2/y) and mass inventory (∼200 Gg/y) in the GOT on the hundred-year timescale were of the same order of magnitude compared with other oceanic margins, and thus the tropical shelf sediments from SE Asia could serve as an important sink of land-emitted BC.

The online measured black carbon aerosol and source orientations in the Nam Co region, Tibet.

PubMed

Zhang, Xin; Ming, Jing; Li, Zhongqin; Wang, Feiteng; Zhang, Guoshuai

2017-11-01

Equivalent black carbon (eBC) mass concentrations were measured by an aethalometer (AE-31) in the Nam Co, central Tibet from 2010 to 2014. Different from previous filter-sampling studies (Ming et al., J Environ Sci 22(11):1748-1756, 2010; Zhao et al., Environ Sci Pollut Res 20:5827-5838, 2013), the first high-resolution online eBC measurement conducted in central Tibet is reported here, allowing to discuss the diurnal variations as well as seasonal variabilities of eBC. Average daily eBC concentration was 74 ± 50 ng/m 3 , reflecting a global background level. Meteorological conditions influenced eBC concentrations largely at seasonal scale, which are higher in February-May but lower in June-January. The highest eBC concentrations (greater than 210 ng/m 3 ) were more associated with the W and WSW winds smaller than 6 m/s. The diurnal variations of eBC showed plateaus from 10:00 to 15:00 with seasonal variations, associated with local anthropogenic activities, such as indigenous Tibetan burning animal waste and tourism traffic. The PBLHs showed a co-variance with eBC concentrations, implicating close sources. The aerosol optical depths derived from the MODIS data over the Nam Co Observatory Station (NCOS)-included sub-area (30° N-40° N, 90° E-100° E) showed significant relationship with eBC concentrations. This suggests that nearby or short-distance sources other than long-distance transported pollutants could be important contributors to eBC concentrations at the NCOS, different from the conclusions suggested by previous studies.

Impact of Snow Grain Shape and Internal Mixing with Black Carbon Aerosol on Snow Optical Properties for use in Climate Models

NASA Astrophysics Data System (ADS)

He, C.; Liou, K. N.; Takano, Y.; Yang, P.; Li, Q.; Chen, F.

2017-12-01

A set of parameterizations is developed for spectral single-scattering properties of clean and black carbon (BC)-contaminated snow based on geometric-optic surface-wave (GOS) computations, which explicitly resolves BC-snow internal mixing and various snow grain shapes. GOS calculations show that, compared with nonspherical grains, volume-equivalent snow spheres show up to 20% larger asymmetry factors and hence stronger forward scattering, particularly at wavelengths <1 mm. In contrast, snow grain sizes have a rather small impact on the asymmetry factor at wavelengths <1 mm, whereas size effects are important at longer wavelengths. The snow asymmetry factor is parameterized as a function of effective size, aspect ratio, and shape factor, and shows excellent agreement with GOS calculations. According to GOS calculations, the single-scattering coalbedo of pure snow is predominantly affected by grain sizes, rather than grain shapes, with higher values for larger grains. The snow single-scattering coalbedo is parameterized in terms of the effective size that combines shape and size effects, with an accuracy of >99%. Based on GOS calculations, BC-snow internal mixing enhances the snow single-scattering coalbedo at wavelengths <1 mm, but it does not alter the snow asymmetry factor. The BC-induced enhancement ratio of snow single-scattering coalbedo, independent of snow grain size and shape, is parameterized as a function of BC concentration with an accuracy of >99%. Overall, in addition to snow grain size, both BC-snow internal mixing and snow grain shape play critical roles in quantifying BC effects on snow optical properties. The present parameterizations can be conveniently applied to snow, land surface, and climate models including snowpack radiative transfer processes.

Radiative effects of light-absorbing particles deposited in snow over Himalayas using WRF-Chem simulations

NASA Astrophysics Data System (ADS)

Sarangi, C.; Qian, Y.; Painter, T. H.; Liu, Y.; Lin, G.; Wang, H.

2017-12-01

Radiative forcing induced by light-absorbing particles (LAP) deposited on snow is an important surface forcing. It has been debated that an aerosol-induced increase in atmospheric and surface warming over Tibetan Plateau (TP) prior to the South Asian summer monsoon can have a significant effect on the regional thermodynamics and South Asian monsoon circulation. However, knowledge about the radiative effects due to deposition of LAP in snow over TP is limited. In this study we have used a high-resolution WRF-Chem (coupled with online chemistry and snow-LAP-radiation model) simulations during 2013-2014 to estimate the spatio-temporal variation in LAP deposition on snow, specifically black carbon (BC) and dust particles, in Himalayas. Simulated distributions in meteorology, aerosol concentrations, snow albedo, snow grain size and snow depth are evaluated against satellite and in-situ measurements. The spatio-temporal change in snow albedo and snow grain size with variation in LAP deposition is investigated and the resulting shortwave LAP radiative forcing at surface is calculated. The LAP-radiative forcing due to aerosol deposition, both BC and dust, is higher in magnitude over Himalayan slopes (terrain height below 4 km) compared to that over TP (terrain height above 4 km). We found that the shortwave aerosol radiative forcing efficiency at surface due to increase in deposited mass of BC particles in snow layer ( 25 (W/m2)/ (mg/m2)) is manifold higher than the efficiency of dust particles ( 0.1 (W/m2)/ (mg/m2)) over TP. However, the radiative forcing of dust deposited in snow is similar in magnitude (maximum 20-30 W/m2) to that of BC deposited in snow over TP. This is mainly because the amount of dust deposited in snow over TP can be about 100 times greater than the amount of BC deposited in snow during polluted conditions. The impact of LAP on surface energy balance, snow melting and atmospheric thermodynamics is also examined.

The Ascension Island Boundary Layer in the Remote Southeast Atlantic is Often Smoky

NASA Astrophysics Data System (ADS)

Zuidema, Paquita; Sedlacek, Arthur J.; Flynn, Connor; Springston, Stephen; Delgadillo, Rodrigo; Zhang, Jianhao; Aiken, Allison C.; Koontz, Annette; Muradyan, Paytsar

2018-05-01

Observations from June to October 2016, from a surface-based ARM Mobile Facility deployment on Ascension Island (8°S, 14.5°W) indicate that refractory black carbon (rBC) is almost always present within the boundary layer. The rBC mass concentrations, light absorption coefficients, and cloud condensation nuclei concentrations vary in concert and synoptically, peaking in August. Light absorption coefficients at three visible wavelengths as a function of rBC mass are approximately double that calculated from black carbon in lab studies. A spectrally-flat absorption angstrom exponent suggests most of the light absorption is from lens-coated black carbon. The single-scattering-albedo increases systematically from August to October in both 2016 and 2017, with monthly means of 0.78 ± 0.02 (August), 0.81 ± 0.03 (September), and 0.83 ± 0.03 (October) at the green wavelength. Boundary layer aerosol loadings are only loosely correlated with total aerosol optical depth, with smoke more likely to be present in the boundary layer earlier in the biomass burning season, evolving to smoke predominantly present above the cloud layers in September-October, typically resting upon the cloud top inversion. The time period with the campaign-maximum near-surface light absorption and column aerosol optical depth, on 13-16 August 2016, is investigated further. Backtrajectories that indicate more direct boundary layer transport westward from the African continent is central to explaining the elevated surface aerosol loadings.

Distribution and Fate of Black Carbon Nanoparticles from Regional Urban Pollution and Wildfire at a Large Subalpine Lake in the Western United States

NASA Astrophysics Data System (ADS)

Bisiaux, M. M.; Heyvaert, A. C.; Edwards, R.

2012-04-01

Emitted to the atmosphere through fire and fossil fuel combustion, refractory black carbon nanoparticles (rBC) impact human health, climate, atmospheric chemistry, and the carbon cycle. Eventually these particles enter aquatic environments, where their distribution, fate and association with other pollutants are still poorly characterized. This study presents results from an evaluation of rBC in the waters of oligotrophic Lake Tahoe and its watershed in the western United States. The study period included a large wildfire within the Tahoe basin, seasonal snowmelt, and a number of storm events that resulted in pulsed urban runoff into the lake with rBC concentrations up to four orders of magnitude higher than mid-lake concentrations. The results show that elevated rBC concentrations from wildfire and urban runoff were rapidly attenuated in the lake, suggesting unexpected aggregation or degradation of the particles that prevent rBC concentrations from building up in the water of this lake, renowned for its clarity. The rBC concentrations were also measured in sediment cores from Lake Tahoe to evaluate the sediment archive as a potential combustion record. The evidence suggests that rBC is efficiently transferred to these sediments, which preserve a local-to-regional scale history of rBC emissions, as revealed by comparison with other pollutant records in the sediment. Rapid removal of rBC soon after entry into the lake has implications for transport of rBC in the global aquatic environment and flux of rBC from continents to the global ocean.

Investigating the Vertical Distribution and Source Attribution of Black Carbon over the Pacific Ocean

NASA Astrophysics Data System (ADS)

Zhang, J.; Liu, J.; Ban-Weiss, G. A.; Tao, S.

2014-12-01

Long-range transport of black carbon (BC) aerosols to the Pacific Ocean can potentially play a significant role in changing the marine climate through influences on temperature and cloud profiles and the top-of-atmosphere and surface energy balance. Therefore, quantitatively understanding sources of BC over the Pacific, particularly at different altitudes, is of great importance. In this study, we simulate the transport of thirteen continental BC tracers with a variety of e-folding aging times (few hours to 1 month) using the global chemical transport model MOZART-4. We then optimize BC aging rate according to different source regions by constraining the vertical profile of BC concentrations to the HAIPER Polo-to-Pole Observations (HIPPO). We find that for all HIPPO deployments, a shorter BC aging timescale (less than half day) for tropical and mid-latitude tracers and a longer aging timescale (2-10 days) for high-latitude tracers (except summer) in most cases significantly reduces model biases. By comparing the source-receptor relationship between the optimized BC tracers over the Pacific, we find that during 2009-2011, East Asia contributes most to the BC loading over the Northern Pacific in all seasons except summer, while South American, African and Australian tracers dominate the BC loadings over the Southern Pacific. In addition, unlike other tracers, African BC is a dominant contributor over a larger area in the free troposphere versus the boundary layer. Our findings indicate that the aging rate of BC strongly depends on source location and season, which may significantly influence the contribution of different source regions to BC forcing over the Pacific Ocean.

Black carbon radiative forcing derived from AERONET measurements and models over an urban location in the southeastern Iberian Peninsula

NASA Astrophysics Data System (ADS)

Valenzuela, A.; Arola, A.; Antón, M.; Quirantes, A.; Alados-Arboledas, L.

2017-07-01

This paper provides an account of observed variations in Black carbon (BC) aerosol concentrations and their induced radiative forcing for the first time over Granada a measurement site in Southeastern Iberian Peninsula. Column-integrated BC concentrations were retrieved for the period 2005-2012. Monthly averages of BC concentrations (± one standard deviation) ranged from higher values in January and December with 4.0 ± 2.5 and 4 ± 3 mg/m2, respectively, to lower values in July and August with 1.6 ± 1.2 and 2.0 ± 0.5 mg/m2, respectively. This reduction is not only observed in the average values, but also in the median, third and first quartiles. The average BC concentration in winter (3.8 ± 0.6 mg/m2) was substantially higher than in summer (1.9 ± 0.3 mg/m2), being the eight-year average of 2.9 ± 0.9 mg/m2. The reduction in the use of fossil fuels during the economic crisis contributed significantly to reduced atmospheric loadings of BC. According to our analysis this situation persisted until 2010. BC concentration values were analyzed in terms of air mass influence using cluster analysis. BC concentrations for cluster 1 (local and regional areas) showed high correlations with air masses frequency in winter and autumn. In these seasons BC sources were related to the intense road traffic and increased BC emissions from domestic heating. High BC concentrations were found in autumn just when air mass frequencies for cluster 3 (Mediterranean region) were more elevated, suggesting that air masses coming from that area transport biomass burning particles towards Granada. BC aerosol optical properties were retrieved from BC fraction using aerosol AERONET size volume distribution and Mie theory. A radiative transfer model (SBDART) was used to estimate the aerosol radiative forcing separately for composite aerosol (total aerosols) and exclusively for BC aerosols. The mean radiative forcing for composite aerosol was + 23 ± 6 W/m2 (heating rate of + 0.21 ± 0.06 K/day) and + 15 ± 6 W/m2 for BC aerosol (heating rate of + 0.15 ± 0.06 K/day). These values of radiative forcing and heating rate for BC aerosol represent about 70% of their values for composite aerosol, which highlights the crucial role that BC aerosols play in modifying the radiation budget and climate.

Different patterns of nuclear and mitochondrial penetration by the G3 PAMAM dendrimer and its biotin–pyridoxal bioconjugate BC-PAMAM in normal and cancer cells in vitro

PubMed Central

Uram, Łukasz; Szuster, Magdalena; Filipowicz, Aleksandra; Gargasz, Krzysztof; Wołowiec, Stanisław; Wałajtys-Rode, Elżbieta

2015-01-01

The intracellular localization and colocalization of a fluorescently labeled G3 amine-terminated cationic polyamidoamine (PAMAM) dendrimer and its biotin–pyridoxal (BC-PAMAM) bioconjugate were investigated in a concentration-dependent manner in normal human fibroblast (BJ) and squamous epithelial carcinoma (SCC-15) cell lines. After 24 hours treatment, both cell lines revealed different patterns of intracellular dendrimer accumulation depending on their cytotoxic effects. Cancer cells exhibited much higher (20-fold) tolerance for native PAMAM treatment than fibroblasts, whereas BC-PAMAM was significantly toxic only for fibroblasts at 50 µM concentration. Fibroblasts accumulated the native and bioconjugated dendrimers in a concentration-dependent manner at nontoxic range of concentration, with significantly lower bioconjugate loading. After reaching the cytotoxicity level, fluorescein isothiocyanate-PAMAM accumulation remains at high, comparable level. In cancer cells, native PAMAM loading at higher, but not cytotoxic concentrations, was kept at constant level with a sharp increase at toxic concentration. Mander’s coefficient calculated for fibroblasts and cancer cells confirmed more efficient native PAMAM penetration as compared to BC-PAMAM. Significant differences in nuclear dendrimer penetration were observed for both cell lines. In cancer cells, PAMAM signals amounted to ~25%–35% of the total nuclei area at all investigated concentrations, with lower level (15%–25%) observed for BC-PAMAM. In fibroblasts, the dendrimer nuclear signal amounted to 15% at nontoxic and up to 70% at toxic concentrations, whereas BC-PAMAM remained at a lower concentration-dependent level (0.3%–20%). Mitochondrial localization of PAMAM and BC-PAMAM revealed similar patterns in both cell lines, depending on the extracellular dendrimer concentration, and presented significantly lower signals from BC-PAMAM, which correlated well with the cytotoxicity. PMID:26379435

Cellulose Nanofibrils and Mechanism of their Mineralization in Biomimetic Synthesis of Hydroxyapatite/Native Bacterial Cellulose Nanocomposites: Molecular Dynamics Simulations.

PubMed

Lukasheva, N V; Tolmachev, D A

2016-01-12

Molecular dynamics (MD) simulation of a nanofibril of native bacterial cellulose (BC) in solutions of mineral ions is presented. The supersaturated calcium-phosphate (CP) solution with the ionic composition of hydroxyapatite and CaCl2 solutions with the concentrations below, equal to, and above the solubility limits are simulated. The influence of solvation models (TIP3P and TIP4P-ew water models) on structural characteristics of the simulated nanofibril and on the crystal nucleation process is assessed. The structural characteristics of cellulose nanofibrils (in particular, of the surface layer) are found to be nearly independent of the solvation models used in the simulation and on the presence of ions in the solutions. It is shown that ionic clusters are formed in the solution rather than on the fibril surface. The cluster sizes are slightly different for the two water models. The effect of the ion-ion interaction parameters on the results is discussed. The main conclusion is that the activity of hydroxyl groups on the BC fibril surface is not high enough to cause adsorption of Ca(2+) ions from the solution. Therefore, the nucleation of CP crystals takes place initially in solution, and then the crystallites formed can be adsorbed on BC nanofibril surfaces.

Black Carbon in Sedimentary Organic Carbon in the Northeast Pacific using the Benzene Polycarboxylic Acid Method

NASA Astrophysics Data System (ADS)

Coppola, A. I.; Ziolkowski, L. A.; Druffel, E. R.

2010-12-01

Black carbon (BC) in the Northeast Pacific ultrafiltered dissolved organic matter (UDOM) was found to be surprisingly old with a 14C age of 18,000 +/-3,000 14C years (Ziolkowski and Druffel, 2010) using the Benzene Polycarboxylic Acid (BPCA) method, while BC in sedimentary organic carbon (SOC) was found to be 2,400-12,900 14C years older than non-BC SOC (Masiello and Druffel, 1998) with a different method. Using the dichromate-sulfuric acid oxidation method (Wolbach and Anders, 1989), Masiello and Druffel (1998) estimated that 12-31% of SOC in the Northeast Pacific and the Southern Ocean surface sediments was black carbon (BC). However, the dichromate-sulfuric acid oxidation may over-estimate the concentration of BC, because this method is more biased toward modern (char) material (Currie et al., 2002). Alternatively, the BPCA method isolates aromatic components of BC as benzene rings substituted with carboxylic acid groups, and provides structural information about the BC. Recent modifications to the BPCA method by Ziolkowski and Druffel (2009) involve few biases in quantifying BC in the continuum between char and soot in UDOM. Here we use the BPCA method to determine the concentrations and 14C values of BC in sediments from three sites in the Northeast Pacific Ocean. Constraining the difference between non-BC SOC and BC-SOC using the BPCA method allows for a more precise estimate of how much BC is present in the sediments and its 14C age. Presumably, the intermediate reservoir of BC is oceanic dissolved organic carbon (DOC) and is, in part, responsible for DOC’s great 14C age. These results can be utilized to better constrain the oceanic carbon budget as a possible sink of BC. References: Currie, L. A., Benner Jr., B. A., Kessler, J.D., et al (2002), A critical evaluation of interlaboratory data on total, elemental, and isotopic carbon in the carbonaceous particle reference material, nist srm 1649a, J. Res. Natl. Inst. Stand. Technol., 107, 279-298. Masiello, C., and E. R. Druffel (1988), Black carbon in deep-sea sediments, Science, 280, 1911-1913. Wolbach, W., and E. Anders (1989), Elemental carbon in sediments: Determination and isotopic analysis in presence of kerogen, Geochim. Cosmochim. Acta, 53, 1637-1647. Ziolkowski, L. A., and E. R. Druffel (2010), Aged black carbon identified in marine dissolved organic carbon, J. Geophys. Res., 37, L16601, doi: 10.1029/2010GL043963.

Black carbon in the atmosphere and deposition on snow, last 130 years

NASA Astrophysics Data System (ADS)

Skeie, R. B.; Berntsen, T.; Myhre, G.; Pedersen, C.; Gerland, S.; Ström, J.; Forsström, S.

2009-04-01

The transport of Black Carbon (BC) in the atmosphere and the deposition of BC on snow surfaces for the last 130 years, with special emphasis on the last 8 years, are modeled with the Oslo CTM2 model. In addition regional contribution to BC deposition on snow in the polar region is evaluated for some years. The model results are compared with observations including our own recent measurement of BC in snow. Radiative forcing due to the direct effect as well as the snow-albedo effect is also calculated. Oslo CTM2 is an offline chemical transport model with T42 horizontal resolution using meteorological data from the IFS model at ECMWF. The scheme for BC includes hydrophilic and hydrophobic particles, as well as emissions from fossil fuel, biofuel and open biomass burning. Data on snow fall, melt and evaporation from ECMWF are used to generate and remove snow layers in each grid box. In these snow layers the amounts of deposited BC are stored, and concentration of BC in each snow layer is calculated. For the period 1870-2000 time slice simulations are done every 10th year. The period is simulated with constant meteorological data for the year 2000-2001 and vertical resolution of 40 levels. The emission data used is from Bond [1] for fossil fuel and biofuel, and data from Ito and Penner [2] for open biomass burning. The period 2000 until present are modeled with real time meteorological data and vertical resolution of 60 levels. Fossil fuel emission data used are the year 2000 data from Bond [1] except for the Asian region where REAS emissions [3] are used. For biomass burning BC emission the GFED data set are used [4]. The results are compared with available BC measurements from ice cores, air and snow. The observed time history of the BC concentration in snow over Greenland, US, and Himalaya is compared to the model results. During the years 2006-2008 several measurements of BC concentrations in snow in the Arctic region have been done, showing significant spatial variability. Within the large spread in the observations of BC concentration in snow, the model gives results that are consistent with the observations. In addition to evaluating total effect of BC in snow and its radiative effects, regional contribution to BC deposition on snow in the Arctic region are calculated. Today China is the region with largest BC fossil fuel emissions. Our results using the Olso CTM2 model show however that it is the 4th region in contribution to BC deposition on snow north of 65 degrees. The largest contributor is Russia, followed by Western Europe and North America. In the historical period, the share of emissions between these regions differs from the present situation. The BC emissions from fossil fuel in North America and Western Europe were respectively 3 and 2 times larger in 1920-30 than the present emissions from these regions. Therefore those regions had a higher contribution to BC in snow in the Arctic region 80 years ago than they have today. References: 1. Bond, T.C., et al., Historical emissions of black and organic carbon aerosol from energy-related combustion, 1850-2000. Global Biogeochemical Cycles, 2007. 21(2): p. 16. 2. Ito, A. and J.E. Penner, Historical emissions of carbonaceous aerosols from biomass and fossil fuel burning for the period 1870-2000. Global Biogeochemical Cycles, 2005. 19(2): p. 14. 3. Ohara, T., et al., An Asian emission inventory of anthropogenic emission sources for the period 1980-2020. Atmospheric Chemistry and Physics, 2007. 7(16): p. 4419-4444. 4. van der Werf, G.R., et al., Interannual variability in global biomass burning emissions from 1997 to 2004. Atmos. Chem. Phys., 2006. 6(11): p. 3423-3441.

Cloning, monoclonal antibody production, and bodily distribution pattern of a bovine lipocalin.

PubMed

Japaridze, Tamar; Senda, Akitsugu; Nozaki, Hirofumi; Yanagida, Mayumi; Suzuki, Takumi; Ganzorig, Khuukhenbaatar; Kushi, Yasunori; Kida, Katsuya; Urashima, Tadasu; Bruckmaier, Rupert M; Fukuda, Kenji

2012-01-01

A bovine lipocalin, previously identified as a putative odorant-binding protein in bovine colostrum (bcOBP), was cloned and expressed, and its monoclonal antibody was established. bcOBP was constantly secreted into milk on day of parturition until at least 10 d postpartum at a concentration of 181±39 µg/L. Besides milk, bcOBP occurred in the nasal mucus, saliva, amniotic fluid, vaginal discharge, and blood plasma. Despite its low concentration, the distribution pattern and the finding that bcOBP harbored a characteristic sequence motif, CxxxC, which is conserved among insect and mammal pheromone binding proteins, suggest that bcOBP functions as a pheromone carrier. The presence of bcOBP in the plasma at varied concentrations depending on the lactation period does not exclude the possibility that bcOBP is secreted into milk from the blood. Cross-reactivity of the monoclonal antibody indicated presence of proteins homologous to bcOBP in the colostrum of farm animals of Cetartiodactyla.

Components of Particle Emissions from Light-Duty Spark-Ignition Vehicles with Varying Aromatic Content and Octane Rating in Gasoline.

PubMed

Short, Daniel Z; Vu, Diep; Durbin, Thomas D; Karavalakis, Georgios; Asa-Awuku, Akua

2015-09-01

Typical gasoline consists of varying concentrations of aromatic hydrocarbons and octane ratings. However, their impacts on particulate matter (PM) such as black carbon (BC) and water-soluble and insoluble particle compositions are not well-defined. This study tests seven 2012 model year vehicles, which include one port fuel injection (PFI) configured hybrid vehicle, one PFI vehicle, and six gasoline direct injection (GDI) vehicles. Each vehicle was driven on the Unified transient testing cycle (UC) using four different fuels. Three fuels had a constant octane rating of 87 with varied aromatic concentrations at 15%, 25%, and 35%. A fourth fuel with higher octane rating, 91, contained 35% aromatics. BC, PM mass, surface tension, and water-soluble organic mass (WSOM) fractions were measured. The water-insoluble mass (WIM) fraction of the vehicle emissions was estimated. Increasing fuel aromatic content increases BC emission factors (EFs) of transient cycles. BC concentrations were higher for the GDI vehicles than the PFI and hybrid vehicles, suggesting a potential climate impact for increased GDI vehicle production. Vehicle steady-state testing showed that the hygroscopicity of PM emissions at high speeds (70 mph; κ > 1) are much larger than emissions at low speeds (30 mph; κ < 0.1). Iso-paraffin content in the fuels was correlated to the decrease in WSOM emissions. Both aromatic content and vehicle speed increase the amount of hygroscopic material found in particle emissions.

Black carbon at a roadside site in Beijing: Temporal variations and relationships with carbon monoxide and particle number size distribution

NASA Astrophysics Data System (ADS)

Song, Shaojie; Wu, Ye; Xu, Jiayu; Ohara, Toshimasa; Hasegawa, Shuichi; Li, Jiaqi; Yang, Liu; Hao, Jiming

2013-10-01

Black carbon (BC), carbon monoxide (CO), and particle number size distribution were measured near a major urban expressway of Beijing during summer and winter field campaigns in 2009. BC was also observed at urban and rural sites. The temporal variations of BC and its relationships with CO and particle number size distribution were analyzed. The average BC concentrations at the roadside site were 12.3 and 17.9 μg m-3 during the summer and winter campaigns, respectively. BC concentrations ranked in the order of roadside > urban > rural. A general diurnal pattern at all sites showed that the higher BC levels were observed at night. The diurnal pattern of summertime BC at the roadside site followed the variations of heavy-duty diesel vehicles (HDDVs). The increased proportion of HDDVs at night contributed to high ΔBC/ΔCO ratios. This study suggests that HDDVs are an important contributor to nighttime BC and particle number concentrations of both Aitken and accumulation modes near major roadways in Beijing, especially in summer.

A cellphone based system for large-scale monitoring of black carbon

NASA Astrophysics Data System (ADS)

Ramanathan, N.; Lukac, M.; Ahmed, T.; Kar, A.; Praveen, P. S.; Honles, T.; Leong, I.; Rehman, I. H.; Schauer, J. J.; Ramanathan, V.

2011-08-01

Black carbon aerosols are a major component of soot and are also a major contributor to global and regional climate change. Reliable and cost-effective systems to measure near-surface black carbon (BC) mass concentrations (hereafter denoted as [BC]) globally are necessary to validate air pollution and climate models and to evaluate the effectiveness of BC mitigation actions. Toward this goal we describe a new wireless, low-cost, ultra low-power, BC cellphone based monitoring system (BC_CBM). BC_CBM integrates a Miniaturized Aerosol filter Sampler (MAS) with a cellphone for filter image collection, transmission and image analysis for determining [BC] in real time. The BC aerosols in the air accumulate on the MAS quartz filter, resulting in a coloration of the filter. A photograph of the filter is captured by the cellphone camera and transmitted by the cellphone to the analytics component of BC_CBM. The analytics component compares the image with a calibrated reference scale (also included in the photograph) to estimate [BC]. We demonstrate with field data collected from vastly differing environments, ranging from southern California to rural regions in the Indo-Gangetic plains of Northern India, that the total BC deposited on the filter is directly and uniquely related to the reflectance of the filter in the red wavelength, irrespective of its source or how the particles were deposited. [BC] varied from 0.1 to 1 μg m -3 in Southern California and from 10 to 200 μg m -3 in rural India in our field studies. In spite of the 3 orders of magnitude variation in [BC], the BC_CBM system was able to determine the [BC] well within the experimental error of two independent reference instruments for both indoor air and outdoor ambient air. Accurate, global-scale measurements of [BC] in urban and remote rural locations, enabled by the wireless, low-cost, ultra low-power operation of BC_CBM, will make it possible to better capture the large spatial and temporal variations in [BC], informing climate science, health, and policy.

Global Air Quality and Health Co-benefits of Mitigating Near-Term Climate Change through Methane and Black Carbon Emission Controls

PubMed Central

Schwartz, Joel; Shindell, Drew; Amann, Markus; Faluvegi, Greg; Klimont, Zbigniew; Janssens-Maenhout, Greet; Pozzoli, Luca; Van Dingenen, Rita; Vignati, Elisabetta; Emberson, Lisa; Muller, Nicholas Z.; West, J. Jason; Williams, Martin; Demkine, Volodymyr; Hicks, W. Kevin; Kuylenstierna, Johan; Raes, Frank; Ramanathan, Veerabhadran

2012-01-01

Background: Tropospheric ozone and black carbon (BC), a component of fine particulate matter (PM ≤ 2.5 µm in aerodynamic diameter; PM2.5), are associated with premature mortality and they disrupt global and regional climate. Objectives: We examined the air quality and health benefits of 14 specific emission control measures targeting BC and methane, an ozone precursor, that were selected because of their potential to reduce the rate of climate change over the next 20–40 years. Methods: We simulated the impacts of mitigation measures on outdoor concentrations of PM2.5 and ozone using two composition-climate models, and calculated associated changes in premature PM2.5- and ozone-related deaths using epidemiologically derived concentration–response functions. Results: We estimated that, for PM2.5 and ozone, respectively, fully implementing these measures could reduce global population-weighted average surface concentrations by 23–34% and 7–17% and avoid 0.6–4.4 and 0.04–0.52 million annual premature deaths globally in 2030. More than 80% of the health benefits are estimated to occur in Asia. We estimated that BC mitigation measures would achieve approximately 98% of the deaths that would be avoided if all BC and methane mitigation measures were implemented, due to reduced BC and associated reductions of nonmethane ozone precursor and organic carbon emissions as well as stronger mortality relationships for PM2.5 relative to ozone. Although subject to large uncertainty, these estimates and conclusions are not strongly dependent on assumptions for the concentration–response function. Conclusions: In addition to climate benefits, our findings indicate that the methane and BC emission control measures would have substantial co-benefits for air quality and public health worldwide, potentially reversing trends of increasing air pollution concentrations and mortality in Africa and South, West, and Central Asia. These projected benefits are independent of carbon dioxide mitigation measures. Benefits of BC measures are underestimated because we did not account for benefits from reduced indoor exposures and because outdoor exposure estimates were limited by model spatial resolution. PMID:22418651

Effect of vitamin supplementation on breast milk concentrations of retinol, carotenoids, and tocopherols in HIV-infected Tanzanian women

PubMed Central

Webb, Aimee L.; Aboud, Said; Furtado, Jeremy; Murrin, Clare; Campos, Hannia; Fawzi, Wafaie W.; Villamor, Eduardo

2011-01-01

Background The effect of daily prenatal and postnatal vitamin supplementation on concentrations of breast milk nutrients is not well characterized in HIV-infected women. Objective We examined the impact of vitamin supplementation during pregnancy and lactation on breast milk concentrations of retinol, carotenoids, and tocopherols during the first year post-partum among 626 HIV-infected Tanzanian women. Design We conducted a randomized, double-blind, placebo controlled trial. Women were assigned to one of four daily oral supplements: vitamin A + β-carotene (VA+BC); multivitamins (B, C, E (MV)); MV+VA+BC; or placebo. Concentrations of breast milk nutrients were determined by HPLC at birth and every 3 mo thereafter. Results Supplementation with VA+BC increased concentrations of retinol, β-carotene, and α-carotene at delivery by 4799, 1791, and 84 nmol/L, respectively, compared to no VA+BC (all p<0.0001). MV supplementation did not increase concentrations of α-tocopherol or δ-tocopherol at delivery but significantly decreased concentrations of breast milk γ-tocopherol and retinol. Although concentrations of all nutrients decreased significantly by 3 months postpartum, retinol, α-carotene, and β-carotene concentrations were significantly higher among those receiving VA+BC at 3, 6, and 12 mo compared to no VA+BC. Alpha tocopherol was significantly higher, while γ-tocopherol concentrations were significantly lower, among women receiving MV compared to no MV at 3, 6, and 12 mo post-partum. Conclusions Sustained supplementation of HIV-infected breastfeeding mothers with MV could be a safe and effective intervention to improve vitamin E concentrations in breast milk. VA+BC supplementation increases concentrations of breast milk retinol but it is not recommended in HIV-infected mothers due to the elevated risk of vertical transmission. PMID:17940544

Effect of vitamin supplementation on breast milk concentrations of retinol, carotenoids and tocopherols in HIV-infected Tanzanian women.

PubMed

Webb, A L; Aboud, S; Furtado, J; Murrin, C; Campos, H; Fawzi, W W; Villamor, E

2009-03-01

The effect of daily prenatal and postnatal vitamin supplementation on concentrations of breast milk nutrients is not well characterized in HIV-infected women. We examined the impact of vitamin supplementation during pregnancy and lactation on breast milk concentrations of retinol, carotenoids and tocopherols during the first year postpartum among 626 HIV-infected Tanzanian women. We conducted a randomized, double-blind, placebo-controlled trial. Women were assigned to one of four daily oral supplements: vitamin A+beta-carotene (VA+BC); multivitamins (MV; B, C and E); MV+VA+BC or placebo. Concentrations of breast milk nutrients were determined by high-performance liquid chromatography at birth and every 3 months thereafter. Supplementation with VA+BC increased concentrations of retinol, beta-carotene and alpha-carotene at delivery by 4799, 1791 and 84 nmol l(-1), respectively, compared to no VA+BC (all P<0.0001). MV supplementation did not increase concentrations of alpha-tocopherol or delta-tocopherol at delivery but significantly decreased concentrations of breast milk gamma-tocopherol and retinol. Although concentrations of all nutrients decreased significantly by 3 months postpartum, retinol, alpha-carotene and beta-carotene concentrations were significantly higher among those receiving VA+BC at 3, 6 and 12 months compared to no VA+BC. alpha-Tocopherol was significantly higher, while gamma-tocopherol concentrations were significantly lower, among women receiving MV compared to no MV at 3, 6 and 12 months postpartum. Sustained supplementation of HIV-infected breastfeeding mothers with MV could be a safe and effective intervention to improve vitamin E concentrations in breast milk. VA+BC supplementation increases concentrations of breast milk retinol but it is not recommended in HIV-infected mothers due to the elevated risk of vertical transmission.

Magnetic adsorbents for the removal of Hg (II) and phenanthrene from aqueous solutions

NASA Astrophysics Data System (ADS)

Isari, Ekavi; Karapanagioti, Hrissi K.; Manariotis, Ioannis D.; Werner, David

2015-04-01

Activated carbon (AC) acts as a strong binding agent that lowers the pollutant concentration and, thus its toxicity. Another promising sorbent material in environmental applications is biochar (BC) which is obtained from the incomplete combustion of carbon-rich biomass under oxygen-limited conditions. Both of these materials could be used as soil or sediment amendments that would lower the toxicity in the aqueous phase. A draw back of this technique is that although the pollutant will remain non- bioavailable for many years being sorbed into these sorbents, it actually stays into the system. The objective of this study was (a) to synthesize a magnetic powdered activated carbon (AC/Fe) and magnetic powdered biochar (BC/Fe) produced from commercial AC1 and AC2 samples and biochar respectively and (b) to evaluate the potential use of AC/Fe and BIO/Fe to remove aqueous Hg (II) or phenanthrene while being magnetically recoverable. The BC was produced from olive pomace. The surface area, the pore volume, and the average pore size of each sorbent were determined using gas (N2) adsorption-desorption cycles and the Brunauer, Emmett, and Teller (BET) equation. Isotherms with 30 adsorption and 20 desorption points were conducted at liquid nitrogen temperature (77K). Open surface area and micropore volume were determined using t-plot method and Harkins & Jura equation. For both AC/Fe, surface area measurements resulted in 66% those of corresponding AC. For BC/Fe, the surface area was 82% that of BC. Batch experiments with all sorbent samples and mercury solutions were conducted at room temperature (25oC) and at pH 5 in order to compare the sorption properties of the materials. Similar tests were performed with phenanthrene solutions. Based on mercury isotherm data, AC/Fe and BC/Fe are effective sorbents but with lower sorption capacity compared to the initial materials (50-75% lower). All these properties point to promising materials that can effectively be used for in-situ environmental remediation and also be recovered.

Effects of Lipids on in Vitro Release and Cellular Uptake of β-Carotene in Nanoemulsion-Based Delivery Systems.

PubMed

Yi, Jiang; Zhong, Fang; Zhang, Yuzhu; Yokoyama, Wallace; Zhao, Liqing

2015-12-23

β-Carotene (BC) nanoemulsions were successfully prepared by microfluidization. BC micellarization was significantly affected by bile salts and pancreatin concentration. Positive and linear correlation was observed between BC release and bile salts concentration. Pancreatin facilitated BC's release in simulated digestion. Compared to the control (bulk oil) (4.6%), nanoemulsion delivery systems significantly improved the micellarization of BC (70.9%). The amount of BC partitioned into micelles was positively proportional to the length of carrier oils. Unsaturated fatty acid (UFA)-rich oils were better than saturated fatty acid (SFA)-rich oils in transferring BC (p < 0.05). No significant difference was observed between monounsaturated fatty acid (MUFA)-rich oils and polyunsaturated fatty acid (PUFA)-rich oils (p > 0.05). A positive and linear relationship between the degree of lipolysis and the release of BC in vitro digestion was observed. Bile salts showed cytotoxicity to Caco-2 cells below 20 times dilution. BC uptake by Caco-2 cells was not affected by fatty acid (FA) compositions in micelles, but BC uptake was proportional to its concentration in the diluted micelle fraction. The results obtained are beneficial to encapsulate and deliver BC or other bioactive lipophilic carotenoids in a wide range of commercial products.

On the rumpling instability in thermal barrier systems

NASA Astrophysics Data System (ADS)

Panat, Rahul Padmakar

Thermal barrier coatings (TBCs) are protective multi-layered metal-ceramic coatings used in hot sections of jet engines and gas turbines. The TBCs are composed of a superalloy substrate, an intermediate metallic bond coat (BC) and a ceramic topcoat. The TBCs are beset by reliability problems arising from delamination of the ceramic topcoat due to various instabilities in the system. The present work examines one such instability of "rumpling", or progressive roughening of the BC surface in the BC-superalloy systems upon high temperature exposure. A combined experimental and analytical approach is taken to study the rumpling phenomenon. Thermal cycling and isothermal experiments are carried out in air and in vacuum to identify the driving force and the kinetics governing rumpling. The experiments show that a nominally flat BC surface rumples to a wavelength of about 60--100 mum, and an amplitude of about 4--8 mum. The rumpling is seen to be relatively insensitive to the initial BC surface morphology. Significant initial flaws are not necessary for rumpling to occur. Further, rumpling occurs even in absence of thermal cycling. To explain BC rumpling, we develop a linear stability model for surface evolution of BCs under a remote stress. The driving force for this process is the in-plane stress in the BC due to its thermal mismatch with the substrate as indicated by the experimental results. The BC volume and BC surface diffusion governs the deformation kinetics. A governing equation is derived that gives the amplitude evolution of BC surface perturbations as a function of time. The analysis establishes a range of wavelengths for which the perturbation amplitude increases at a significantly higher rate as compared with other wavelengths. At the dominant instability wavelength, under low-stress and high-temperature conditions, the model shows that the roughening is caused only by volume diffusion, while smoothing is caused only by surface diffusion. The results from this thermodynamic model agree with the experimental observations quite well. Particular BC material properties and testing conditions are identified that control the BC rumpling and hence an important TBC failure mode. Guidelines to improve TBC performance are presented.

DOE Office of Scientific and Technical Information (OSTI.GOV)

Wang, Mo; Xu, B.; Kaspari, Susan D.

We analyzed refractory black carbon (rBC) in an ice core spanning 1875-2000 AD from Mt. Muztagh Ata, the Eastern Pamirs, using a Single Particle Soot Photometer (SP2). Additionally a pre-existing levoglucosan record from the same ice core was used to differentiate rBC that originated from open fires, energy-related combustion of biomass, and fossil fuel combustion. Mean rBC concentrations increased four-fold since the mid-1970s and reached maximum values at the end of 1980s. The observed decrease of the rBC concentrations during the 1990s was likely driven by the economic recession of former USSR countries in Central Asia. Levoglucosan concentrations showed amore » similar temporal trend to rBC concentrations, exhibiting a large increase around 1980 AD followed by a decrease in the 1990s that was likely due to a decrease in energy-related biomass combustion. The time evolution of levoglucosan/rBC ratios indicated stronger emissions from open fires during the 1940s-1950s, while the increase in rBC during the 1980s-1990s was caused from an increase in energy-related combustion of biomass and fossil fuels.« less

Grey Tienshan Urumqi Glacier No.1 and light-absorbing impurities.

PubMed

Ming, Jing; Xiao, Cunde; Wang, Feiteng; Li, Zhongqin; Li, Yamin

2016-05-01

The Tienshan Urumqi Glacier No.1 (TUG1) usually shows "grey" surfaces in summers. Besides known regional warming, what should be responsible for largely reducing its surface albedo and making it look "grey"? A field campaign was conducted on the TUG1 on a selected cloud-free day of 2013 after a snow fall at night. Fresh and aged snow samples were collected in the field, and snow densities, grain sizes, and spectral reflectances were measured. Light-absorbing impurities (LAIs) including black carbon (BC) and dust, and number concentrations and sizes of the insoluble particles (IPs) in the samples were measured in the laboratory. High temperatures in summer probably enhanced the snow ageing. During the snow ageing process, the snow density varied from 243 to 458 kg m(-3), associated with the snow grain size varying from 290 to 2500 μm. The concentrations of LAIs in aged snow were significantly higher than those in fresh snow. Dust and BC varied from 16 ppm and 25 ppb in fresh snow to 1507 ppm and 1738 ppb in aged snow, respectively. Large albedo difference between the fresh and aged snow suggests a consequent forcing of 180 W m(-2). Simulations under scenarios show that snow ageing, BC, and dust were responsible for 44, 25, and 7 % of the albedo reduction in the accumulation zone, respectively.

Complement activation on the surface of cell-derived microparticles during cardiac surgery with cardiopulmonary bypass - is retransfusion of pericardial blood harmful?

PubMed

Biró, E; van den Goor, J M; de Mol, B A; Schaap, M C; Ko, L-Y; Sturk, A; Hack, C E; Nieuwland, R

2011-01-01

To investigate whether cell-derived microparticles play a role in complement activation in pericardial blood of patients undergoing cardiac surgery with cardiopulmonary bypass (CPB) and whether microparticles in pericardial blood contribute to systemic complement activation upon retransfusion. Pericardial blood of 13 patients was retransfused in 9 and discarded in 4 cases. Microparticles were isolated from systemic blood collected before anesthesia (T1) and at the end of CPB (T2), and from pericardial blood. The microparticles were analyzed by flow cytometry for bound complement components C1q, C4 and C3, and bound complement activator molecules C-reactive protein (CRP), serum amyloid P-component (SAP), immunoglobulin (Ig)M and IgG. Fluid-phase complement activation products (C4b/c, C3b/c) and activator molecules were determined by ELISA. Compared with systemic T1 blood, pericardial blood contained increased C4b/c and C3b/c, and increased levels of microparticles with bound complement components. In systemic T1 samples, microparticle-bound CRP, whereas in pericardial blood, microparticle-bound SAP and IgM were associated with complement activation. At the end of CPB, increased C3b/c (but not C4b/c) was present in systemic T2 blood compared with T1, while concentrations of microparticles binding complement components and of those binding complement activator molecules were similar. Concentrations of fluid-phase complement activation products and microparticles were similar in patients whether or not retransfused with pericardial blood. In pericardial blood of patients undergoing cardiac surgery with CPB, microparticles contribute to activation of the complement system via bound SAP and IgM. Retransfusion of pericardial blood, however, does not contribute to systemic complement activation.

Large reductions in urban black carbon concentrations in the United States between 1965 and 2000

NASA Astrophysics Data System (ADS)

Kirchstetter, Thomas W.; Preble, Chelsea V.; Hadley, Odelle L.; Bond, Tami C.; Apte, Joshua S.

2017-02-01

Long-term pollutant concentration trends can be useful for evaluating air quality effects of emission controls and historical transitions in energy sources. We employed archival records of coefficient of haze (COH), a now-retired measure of light-absorbing particulate matter, to re-construct historical black carbon (BC) concentrations at urban locations in the United States (U.S.). The following relationship between COH and BC was determined by reinstating into service COH monitors beside aethalometers for two years in Vallejo and one year in San Jose, California: BC (μg m-3) = 6.7COH + 0.1, R2 = 0.9. Estimated BC concentrations in ten states stretching from the East to West Coast decreased markedly between 1965 and 1980: 5-fold in Illinois, Ohio, and Virginia, 4-fold in Missouri, and 2.5-fold in Pennsylvania. Over the period from the mid-1960s to the early 2000s, annual average BC concentrations in New Jersey and California decreased from 13 to 2 μg m-3 and 4 to 1 μg m-3, respectively, despite concurrent increases in fossil fuel consumption from 1.6 to 2.1 EJ (EJ = 1018 J) in New Jersey and 4.2 to 6.4 EJ in California. New Jersey's greater reliance on BC-producing heavy fuel oils and coal in the 1960s and early 1970s and subsequent transition to cleaner fuels explains why the decrease was larger in New Jersey than California. Patterns in seasonal and weekly BC concentrations and energy consumption trends together indicate that reducing wintertime emissions - namely substituting natural gas and electricity for heavy fuel oil in the residential sector - and decreasing emissions from diesel vehicles contributed to lower ambient BC concentrations. Over the period of study, declining concentrations of BC, a potent and short-lived climate warming pollutant, contrast increasing fossil fuel carbon dioxide (CO2) emissions in the U.S. Declining BC emissions may have had the benefit of mitigating some atmospheric warming driven by increased CO2 emissions with complementary health benefits.

Size distribution and coating thickness of black carbon from the Canadian oil sands operations

NASA Astrophysics Data System (ADS)

Cheng, Yuan; Li, Shao-Meng; Gordon, Mark; Liu, Peter

2018-02-01

Black carbon (BC) plays an important role in the Earth's climate system. However, parameterizations of BC size and mixing state have not been well addressed in aerosol-climate models, introducing substantial uncertainties into the estimation of radiative forcing by BC. In this study, we focused on BC emissions from the oil sands (OS) surface mining activities in northern Alberta, based on an aircraft campaign conducted over the Athabasca OS region in 2013. A total of 14 flights were made over the OS source area, in which the aircraft was typically flown in a four- or five-sided polygon pattern along flight tracks encircling an OS facility. Another 3 flights were performed downwind of the OS source area, each of which involved at least three intercepting locations where the well-mixed OS plume was measured along flight tracks perpendicular to the wind direction. Comparable size distributions were observed for refractory black carbon (rBC) over and downwind of the OS facilities, with rBC mass median diameters (MMDs) between ˜ 135 and 145 nm that were characteristic of fresh urban emissions. This MMD range corresponded to rBC number median diameters (NMDs) of ˜ 60-70 nm, approximately 100 % higher than the NMD settings in some aerosol-climate models. The typical in- and out-of-plume segments of a flight, which had different rBC concentrations and photochemical ages, showed consistent rBC size distributions in terms of MMD, NMD and the corresponding distribution widths. Moreover, rBC size distributions remained unchanged at different downwind distances from the source area, suggesting that atmospheric aging would not necessarily change rBC size distribution. However, aging indeed influenced rBC mixing state. Coating thickness for rBC cores in the diameter range of 130-160 nm was nearly doubled (from ˜ 20 to 40 nm) within 3 h when the OS plume was transported over a distance of 90 km from the source area.

Towards Soil and Sediment Inventories of Black Carbon

NASA Astrophysics Data System (ADS)

Masiello, C. A.

2008-12-01

A body of literature on black carbon (BC) concentrations in soils and sediments is rapidly accumulating, but as of yet, there are no global or regional inventories of BC in either reservoir. Soil and sediment BC inventories are badly needed for a range of fields. For example, in oceanography a global sediment BC inventory is crucial in understanding the role of biomass burning in the development of stable marine carbon reservoirs, including dissolved organic carbon and sedimentary organic carbon. Again in the marine environment, BC likely strongly impacts the fate and transport of anthropogenic pollutants: regional inventories of BC in sediments will help develop better environmental remediation strategies. In terrestrial systems well-constrained natural BC soil inventories would help refine ecological, agricultural, and soil biogeochemical studies. BC is highly sorptive of nutrients including nitrogen and phosphorous. The presence of BC in ecosystems almost certainly alters N and P cycling; however, without soil BC inventories, we cannot know where BC has a significant impact. BC's nutrient sorptivity and water-holding capacity make it an important component of agricultural soils, and some researchers have proposed artificially increasing soil BC inventories to improve soil fertility. Natural soil BC concentrations in some regions are quite high, but without a baseline inventory, it is challenging to predict when agricultural amendment will significantly exceed natural conditions. And finally, because BC is one of the most stable fractions of organic carbon in soils, understanding its concentration and regional distribution will help us track the dynamics of soil organic matter response to changing environmental conditions. Developing effective regional and global BC inventories is challenging both because of data sparsity and methodological intercomparison issues. In this presentation I will describe a roadmap to generating these valuable inventories.

Multidecadal trends in aerosol radiative forcing over the Arctic: Contribution of changes in anthropogenic aerosol to Arctic warming since 1980

NASA Astrophysics Data System (ADS)

Breider, Thomas J.; Mickley, Loretta J.; Jacob, Daniel J.; Ge, Cui; Wang, Jun; Payer Sulprizio, Melissa; Croft, Betty; Ridley, David A.; McConnell, Joseph R.; Sharma, Sangeeta; Husain, Liaquat; Dutkiewicz, Vincent A.; Eleftheriadis, Konstantinos; Skov, Henrik; Hopke, Phillip K.

2017-03-01

Arctic observations show large decreases in the concentrations of sulfate and black carbon (BC) aerosols since the early 1980s. These near-term climate-forcing pollutants perturb the radiative balance of the atmosphere and may have played an important role in recent Arctic warming. We use the GEOS-Chem global chemical transport model to construct a 3-D representation of Arctic aerosols that is generally consistent with observations and their trends from 1980 to 2010. Observations at Arctic surface sites show significant decreases in sulfate and BC mass concentrations of 2-3% per year. We find that anthropogenic aerosols yield a negative forcing over the Arctic, with an average 2005-2010 Arctic shortwave radiative forcing (RF) of -0.19 ± 0.05 W m-2 at the top of atmosphere (TOA). Anthropogenic sulfate in our study yields more strongly negative forcings over the Arctic troposphere in spring (-1.17 ± 0.10 W m-2) than previously reported. From 1980 to 2010, TOA negative RF by Arctic aerosol declined, from -0.67 ± 0.06 W m-2 to -0.19 ± 0.05 W m-2, yielding a net TOA RF of +0.48 ± 0.06 W m-2. The net positive RF is due almost entirely to decreases in anthropogenic sulfate loading over the Arctic. We estimate that 1980-2010 trends in aerosol-radiation interactions over the Arctic and Northern Hemisphere midlatitudes have contributed a net warming at the Arctic surface of +0.27 ± 0.04 K, roughly one quarter of the observed warming. Our study does not consider BC emissions from gas flaring nor the regional climate response to aerosol-cloud interactions or BC deposition on snow.

Impact of Canadian wildfire smoke on air quality at two rural sites in NY State

NASA Astrophysics Data System (ADS)

Dutkiewicz, Vincent A.; Husain, Liaquat; Roychowdhury, Utpal K.; Demerjian, Kenneth L.

2011-04-01

We report high concentrations of black carbon aerosols (BC), present at two rural sites in New York during the last week in May 2010, that are linked to wildfire activity. At Mayville BC from wood smoke was recorded for a total of 20 h from three separate episodes, mean concentration was 1400 ng m -3. These three short events contributed 13% of the BC burden during the month of May. At Whiteface Mountain high concentrations of BC, carbon monoxide gas (CO), and fine particulate matter mass (PM 2.5) are reported from a heavy smoke event that impacted the Adirondack region of the State on May 31, 2010. PM 2.5 mass recorded at the Lodge site (600 m above mean sea level) was 150 μg m -3 at 8:30 am EST and the 24-h mean was almost twice the USEPA limits while CO concentration exceeded 1000 ppb and BC concentration reached 9600 ng m -3. The event was delayed several hours at the Summit site (1500 m above mean sea level) but at 5:45 pm BC concentration reached 1600 ng m -3 and CO was 317 ppbv. Detailed temporal profiles and correlations are presented.

Latitudinal distribution of aerosol black carbon and its mass fraction to composite aerosols over peninsular India during winter season

NASA Astrophysics Data System (ADS)

Moorthy, K. Krishna; Babu, S. Suresh; Badarinath, K. V. S.; Sunilkumar, S. V.; Kiranchand, T. R.; Ahmed, Y. Nazeer

2007-04-01

During a land campaign to characterise the spatial distribution of aerosols over peninsular India during the winter season, extensive, collocated, and spatially resolved measurements of mass concentration of the composite aerosols (MT) as well as that (MB) of aerosol Black Carbon (BC) were made over different environments (coastal, industrial, urban, village, remote, semiarid) of the western peninsular India. High concentrations of BC, >2.5 μg m-3, were observed along the west coast, from ~8°N up to 14.5°N, and moderate values (1.0 to 2.5 μg m-3) over inland regions from 15 to 18°N. Latitudinally, BC concentration decreased from south to north, @~160 ng m-3 for every degree increase in latitude. The spatial pattern of BC mass fraction differed from that of MB, with regions of high (8 to 16%) ratios spreading more interior, implying higher fractional load of BC at locations where the BC concentrations remain lower.

Cadmium, lead, and zinc mobility and plant uptake in a mine soil amended with sugarcane straw biochar.

PubMed

Puga, A P; Abreu, C A; Melo, L C A; Paz-Ferreiro, J; Beesley, L

2015-11-01

Accumulation of heavy metals in unconsolidated soils can prove toxic to proximal environments, if measures are not taken to stabilize soils. One way to minimize the toxicity of metals in soils is the use of materials capable of immobilizing these contaminants by sorption. Biochar (BC) can retain large amounts of heavy metals due to, among other characteristics, its large surface area. In the current experiment, sugarcane-straw-derived biochar, produced at 700 °C, was applied to a heavy-metal-contaminated mine soil at 1.5, 3.0, and 5.0% (w/w). Jack bean and Mucuna aterrima were grown in pots containing a mine contaminated soil and soil mixed with BC. Pore water was sampled to assess the effects of biochar on zinc solubility, while soils were analyzed by DTPA extraction to confirm available metal concentrations. The application of BC decreased the available concentrations of Cd, Pb, and Zn in the mine contaminated soil leading to a consistent reduction in the concentration of Zn in the pore water. Amendment with BC reduced plant uptake of Cd, Pb, and Zn with the jack bean uptaking higher amounts of Cd and Pb than M. aterrima. This study indicates that biochar application during mine soil remediation could reduce plant concentrations of heavy metals. Coupled with this, symptoms of heavy metal toxicity were absent only in plants growing in pots amended with biochar. The reduction in metal bioavailability and other modifications to the substrate induced by the application of biochar may be beneficial to the establishment of a green cover on top of mine soil to aid remediation and reduce risks.

Trichodesmium slicks associated with environmental conditions of continental shelf-break at the southwestern of the Atlantic Ocean

NASA Astrophysics Data System (ADS)

Detoni, A. M. S.; Yunes, J. S., Sr.; Ciotti, Á. M.; Calil, P. H. R.; Tavano, V. M.

2016-02-01

Trichodesmium can accumulate high biomass, particularly in the oligotrophic regions of North and Tropical Atlantic, and North Pacific. Large Trichodesmium slicks have been reported in the South Atlantic as well, associated with the Brazil Currrent (BC) that flows southwards over the continental shelf-break. Regional variations of the width of the Brazilian continental shelf, as well as changes in the bottom topography, generate cyclonic and anti-cyclonic eddies as BC crosses the southeastern Brazil. Thus, the general conditions of the BC - characterized as a warm, saline and oligotrophic current - are expected to change not only with latitude but also by the influence of mesoscale instabilities. In this study, three oceanographic cruises were carried out to characterize the distribution of Trichodesmium along the southeastern Brazilian continental shelf-break and their relationship with temperature and upper layer nutrients concentrations. As in other oceanic regions, high concentrations of Trichodesmium (maximum 212.6 × 105 trichomes L-1) were observed in waters with temperatures between 22° C to 25° C, low nitrogen (< 2.4 μM), and moderate phosphate concentrations (> 0.08 μM), where wind speeds were low (< 11 m s-1). Generally, slicks were present where phosphate concentration in the upper 25 m was slightly higher than that of adjacent waters. Wind and hydrographic observations suggested that wind divergence at micro-regions (approximately 625 km2), as well as shelf-break dynamics can drive sporadic shelf-break upwelling, favouring Trichodesmium growth between 23° S to 28° S. Although shelf-break upwelling may occur along the entire domain of the BC flow, Trichodesmium densities were low at latitudes between 28° S to 33° S likely a result of the lower sea surface temperature.

Characterization of Ambient Black Carbon Aerosols

NASA Astrophysics Data System (ADS)

Zhang, R.; Levy, M. E.; Zheng, J.; Molina, L. T.

2013-12-01

Because of the strong absorption over a broad range of the electromagnetic spectra, black carbon (BC) is a key short-lived climate forcer, which contributes significantly to climate change by direct radiative forcing and is the second most important component causing global warming after carbon dioxide. The impact of BC on the radiative forcing of the Earth-Atmosphere system is highly dependent of the particle properties. In this presentation, emphasis will be placed on characterizing BC containing aerosols in at the California-Mexico border to obtain a greater understanding of the atmospheric aging and properties of ambient BC aerosols. A comprehensive set of directly measured aerosol properties, including the particle size distribution, effective density, hygroscopicity, volatility, and several optical properties, will be discussed to quantify the mixing state and composition of ambient particles. In Tijuana, Mexico, submicron aerosols are strongly influenced by vehicle emissions; subsequently, the BC concentration in Tijuana is considerably higher than most US cities with an average BC concentration of 2.71 × 2.65 g cm-3. BC accounts for 24.75 % × 9.44 of the total submicron concentration on average, but periodically accounts for over 50%. This high concentration of BC strongly influences many observed aerosol properties such as single scattering albedo, hygroscopicity, effective density, and volatility.

Black carbon aerosol characterization in a remote area of Qinghai-Tibetan Plateau, western China.

PubMed

Wang, Qiyuan; Schwarz, J P; Cao, Junji; Gao, Rushan; Fahey, D W; Hu, Tafeng; Huang, R-J; Han, Yongming; Shen, Zhenxing

2014-05-01

The concentrations, size distributions, and mixing states of refractory black carbon (rBC) aerosols were measured with a ground-based Single Particle Soot Photometer (SP2), and aerosol absorption was measured with an Aethalometer at Qinghai Lake (QHL), a rural area in the Northeastern Tibetan Plateau of China in October 2011. The area was not pristine, with an average rBC mass concentration of 0.36 μg STP-m(-3) during the two-week campaign period. The rBC concentration peaked at night and reached the minimal in the afternoon. This diurnal cycle of concentration is negatively correlated with the mixed layer depth and ventilation. When air masses from the west of QHL were sampled in late afternoon to early evening, the average rBC concentration of 0.21 μg STP-m(-3) was observed, representing the rBC level in a larger Tibetan Plateau region because of the highest mixed layer depth. A lognormal primary mode with mass median diameter (MMD) of ~175 nm, and a small secondary lognormal mode with MMD of 470-500 nm of rBC were observed. Relative reduction in the secondary mode during a snow event supports recent work that suggested size dependent removal of rBC by precipitation. About 50% of the observed rBC cores were identified as thickly coated by non-BC material. A comparison of the Aethalometer and SP2 measurements suggests that non-BC species significantly affect the Aethalometer measurements in this region. A scaling factor for the Aethalometer data at a wavelength of 880 nm is therefore calculated based on the measurements, which may be used to correct other Aethalometer datasets collected in this region for a more accurate estimate of the rBC loading. The results present here significantly improve our understanding of the characteristics of rBC aerosol in the less studied Tibetan Plateau region and further highlight the size dependent removal of BC via precipitation. Copyright © 2014 Elsevier B.V. All rights reserved.

20 years of Black Carbon measurements in Germany

NASA Astrophysics Data System (ADS)

Kutzner, Rebecca; Quedenau, Jörn; Kuik, Friderike; von Schneidemesser, Erika; Schmale, Julia

2016-04-01

Black Carbon (BC) is an important short-lived climate-forcing pollutant contributing to global warming through absorption of sunlight. At the same time, BC, as a component of particulate matter (PM) exerts adverse health effects, like decreased lung function and exacerbated asthma. Globally, anthropogenic emission sources of BC include residential heating, transport, and agricultural fires, while the dominant natural emission sources are wildfires. Despite the various adverse effects of BC, legislation that requires mandatory monitoring of BC concentrations does not currently exist in the European Union. Instead, BC is only indirectly monitored as component of PM10 and PM2.5 (particulate matter with a diameter smaller 10 μm and 2.5 μm). Before the introduction of mandatory PM10 and PM2.5 monitoring in the European Union in 2005 and 2015, respectively, 'black smoke', a surrogate for BC, was a required measurement in Germany from the early 1990s. The annual mean limit value was 14 μg m-3 from 1995 and 8 μg m-3 from 1998 onwards. Many 'black smoke' measurements were stopped in 2004, with the repeal of the regulations obtaining at the time. However, in most German federal states a limited number BC monitoring stations continued to operate. Here we present a synthesis of BC data from 213 stations across Germany covering the period between 1994 and 2014. Due to the lack of a standardized method and respective legislation, the data set is very heterogeneous relying on twelve different measurement methods including chemical, optical, and thermal-optical methods. Stations include locations classified as background, urban-background, industrial and traffic among other types. Raw data in many different formats has been modelled and integrated in a relational database, allowing various options for further data analysis. We highlight results from the year 2009, as it is the year with the largest measurement coverage based on the same measurement method, with 30 stations. In 2009 daily average concentrations at 12 background stations ranged from 0.20 to 9.10 μg m-3 BC, while at traffic sites (15 stations) concentrations ranged from 0.30 to 30.60 μg m-3 BC, and industrial sites (3 stations) showed concentrations ranging between 0.30 and 9.4 μg m-3. The seasonal cycle for the year 2009 shows a similar pattern for industrial and background stations with a tendency of higher concentrations in winter. The concentrations at traffic stations are not as clearly coupled to seasons but have a strong weekly cycle with lower concentrations during weekends. Investigating the trends in BC concentration over at least 10 years was possible for 13 stations. Preliminary results suggest that concentrations have declined at traffic and background stations between 2005 and 2014. This implies that a general reduction of BC has already been achieved. However, preliminary results also show that elevated concentrations still occur during the colder months, most likely linked to residential heating.

Global radiative effects of solid fuel cookstove aerosol emissions

NASA Astrophysics Data System (ADS)

Huang, Yaoxian; Unger, Nadine; Storelvmo, Trude; Harper, Kandice; Zheng, Yiqi; Heyes, Chris

2018-04-01

We apply the NCAR CAM5-Chem global aerosol-climate model to quantify the net global radiative effects of black and organic carbon aerosols from global and Indian solid fuel cookstove emissions for the year 2010. Our assessment accounts for the direct radiative effects, changes to cloud albedo and lifetime (aerosol indirect effect, AIE), impacts on clouds via the vertical temperature profile (semi-direct effect, SDE) and changes in the surface albedo of snow and ice (surface albedo effect). In addition, we provide the first estimate of household solid fuel black carbon emission effects on ice clouds. Anthropogenic emissions are from the IIASA GAINS ECLIPSE V5a inventory. A global dataset of black carbon (BC) and organic aerosol (OA) measurements from surface sites and aerosol optical depth (AOD) from AERONET is used to evaluate the model skill. Compared with observations, the model successfully reproduces the spatial patterns of atmospheric BC and OA concentrations, and agrees with measurements to within a factor of 2. Globally, the simulated AOD agrees well with observations, with a normalized mean bias close to zero. However, the model tends to underestimate AOD over India and China by ˜ 19 ± 4 % but overestimate it over Africa by ˜ 25 ± 11 % (± represents modeled temporal standard deviations for n = 5 run years). Without BC serving as ice nuclei (IN), global and Indian solid fuel cookstove aerosol emissions have net global cooling radiative effects of -141 ± 4 mW m-2 and -12 ± 4 mW m-2, respectively (± represents modeled temporal standard deviations for n = 5 run years). The net radiative impacts are dominated by the AIE and SDE mechanisms, which originate from enhanced cloud condensation nuclei concentrations for the formation of liquid and mixed-phase clouds, and a suppression of convective transport of water vapor from the lower troposphere to the upper troposphere/lower stratosphere that in turn leads to reduced ice cloud formation. When BC is allowed to behave as a source of IN, the net global radiative impacts of the global and Indian solid fuel cookstove emissions range from -275 to +154 mW m-2 and -33 to +24 mW m-2, with globally averaged values of -59 ± 215 and 0.3 ± 29 mW m-2, respectively. Here, the uncertainty range is based on sensitivity simulations that alter the maximum freezing efficiency of BC across a plausible range: 0.01, 0.05 and 0.1. BC-ice cloud interactions lead to substantial increases in high cloud (< 500 hPa) fractions. Thus, the net sign of the impacts of carbonaceous aerosols from solid fuel cookstoves on global climate (warming or cooling) remains ambiguous until improved constraints on BC interactions with mixed-phase and ice clouds are available.

Land use regression modelling of air pollution in high density high rise cities: A case study in Hong Kong.

PubMed

Lee, Martha; Brauer, Michael; Wong, Paulina; Tang, Robert; Tsui, Tsz Him; Choi, Crystal; Cheng, Wei; Lai, Poh-Chin; Tian, Linwei; Thach, Thuan-Quoc; Allen, Ryan; Barratt, Benjamin

2017-08-15

Land use regression (LUR) is a common method of predicting spatial variability of air pollution to estimate exposure. Nitrogen dioxide (NO 2 ), nitric oxide (NO), fine particulate matter (PM 2.5 ), and black carbon (BC) concentrations were measured during two sampling campaigns (April-May and November-January) in Hong Kong (a prototypical high-density high-rise city). Along with 365 potential geospatial predictor variables, these concentrations were used to build two-dimensional land use regression (LUR) models for the territory. Summary statistics for combined measurements over both campaigns were: a) NO 2 (Mean=106μg/m 3 , SD=38.5, N=95), b) NO (M=147μg/m 3 , SD=88.9, N=40), c) PM 2.5 (M=35μg/m 3 , SD=6.3, N=64), and BC (M=10.6μg/m 3 , SD=5.3, N=76). Final LUR models had the following statistics: a) NO 2 (R 2 =0.46, RMSE=28μg/m 3 ) b) NO (R 2 =0.50, RMSE=62μg/m 3 ), c) PM 2.5 (R 2 =0.59; RMSE=4μg/m 3 ), and d) BC (R 2 =0.50, RMSE=4μg/m 3 ). Traditional LUR predictors such as road length, car park density, and land use types were included in most models. The NO 2 prediction surface values were highest in Kowloon and the northern region of Hong Kong Island (downtown Hong Kong). NO showed a similar pattern in the built-up region. Both PM 2.5 and BC predictions exhibited a northwest-southeast gradient, with higher concentrations in the north (close to mainland China). For BC, the port was also an area of elevated predicted concentrations. The results matched with existing literature on spatial variation in concentrations of air pollutants and in relation to important emission sources in Hong Kong. The success of these models suggests LUR is appropriate in high-density, high-rise cities. Copyright © 2017 Elsevier B.V. All rights reserved.

Preparation and evaluation of nanocellulose-gold nanoparticle nanocomposites for SERS applications.

PubMed

Wei, Haoran; Rodriguez, Katia; Renneckar, Scott; Leng, Weinan; Vikesland, Peter J

2015-08-21

Nanocellulose is of research interest due to its extraordinary optical, thermal, and mechanical properties. The incorporation of guest nanoparticles into nanocellulose substrates enables production of novel nanocomposites with a broad range of applications. In this study, gold nanoparticle/bacterial cellulose (AuNP/BC) nanocomposites were prepared and evaluated for their applicability as surface-enhanced Raman scattering (SERS) substrates. The nanocomposites were prepared by citrate mediated in situ reduction of Au(3+) in the presence of a BC hydrogel at 303 K. Both the size and morphology of the AuNPs were functions of the HAuCl4 and citrate concentrations. At high HAuCl4 concentrations, Au nanoplates form within the nanocomposites and are responsible for high SERS enhancements. At lower HAuCl4 concentrations, uniform nanospheres form and the SERS enhancement is dependent on the nanosphere size. The time-resolved increase in the SERS signal was probed as a function of drying time with SERS 'hot-spots' primarily forming in the final minutes of nanocomposite drying. The application of the AuNP/BC nanocomposites for detection of the SERS active dyes MGITC and R6G as well as the environmental contaminant atrazine is illustrated as is its use under low and high pH conditions. The results indicate the broad applicability of this nanocomposite for analyte detection.

Origin of elemental carbon in snow from western Siberia and northwestern European Russia during winter-spring 2014, 2015 and 2016

NASA Astrophysics Data System (ADS)

Evangeliou, Nikolaos; Shevchenko, Vladimir P.; Espen Yttri, Karl; Eckhardt, Sabine; Sollum, Espen; Pokrovsky, Oleg S.; Kobelev, Vasily O.; Korobov, Vladimir B.; Lobanov, Andrey A.; Starodymova, Dina P.; Vorobiev, Sergey N.; Thompson, Rona L.; Stohl, Andreas

2018-01-01

Short-lived climate forcers have been proven important both for the climate and human health. In particular, black carbon (BC) is an important climate forcer both as an aerosol and when deposited on snow and ice surface because of its strong light absorption. This paper presents measurements of elemental carbon (EC; a measurement-based definition of BC) in snow collected from western Siberia and northwestern European Russia during 2014, 2015 and 2016. The Russian Arctic is of great interest to the scientific community due to the large uncertainty of emission sources there. We have determined the major contributing sources of BC in snow in western Siberia and northwestern European Russia using a Lagrangian atmospheric transport model. For the first time, we use a recently developed feature that calculates deposition in backward (so-called retroplume) simulations allowing estimation of the specific locations of sources that contribute to the deposited mass. EC concentrations in snow from western Siberia and northwestern European Russia were highly variable depending on the sampling location. Modelled BC and measured EC were moderately correlated (R = 0.53-0.83) and a systematic region-specific model underestimation was found. The model underestimated observations by 42 % (RMSE = 49 ng g-1) in 2014, 48 % (RMSE = 37 ng g-1) in 2015 and 27 % (RMSE = 43 ng g-1) in 2016. For EC sampled in northwestern European Russia the underestimation by the model was smaller (fractional bias, FB > -100 %). In this region, the major sources were transportation activities and domestic combustion in Finland. When sampling shifted to western Siberia, the model underestimation was more significant (FB < -100 %). There, the sources included emissions from gas flaring as a major contributor to snow BC. The accuracy of the model calculations was also evaluated using two independent datasets of BC measurements in snow covering the entire Arctic. The model underestimated BC concentrations in snow especially for samples collected in springtime.

Acute Respiratory Inflammation in Children and Black Carbon in Ambient Air before and during the 2008 Beijing Olympics

PubMed Central

Lin, Weiwei; Huang, Wei; Hu, Min; Brunekreef, Bert; Zhang, Yuanhang; Liu, Xingang; Cheng, Hong; Gehring, Ulrike; Li, Chengcai; Tang, Xiaoyan

2011-01-01

Background: Epidemiologic evidence for a causative association between black carbon (BC) and health outcomes is limited. Objectives: We estimated associations and exposure–response relationships between acute respiratory inflammation in schoolchildren and concentrations of BC and particulate matter with an aerodynamic diameter of ≤ 2.5 μm (PM2.5) in ambient air before and during the air pollution intervention for the 2008 Beijing Olympics. Methods: We measured exhaled nitric oxide (eNO) as an acute respiratory inflammation biomarker and hourly mean air pollutant concentrations to estimate BC and PM2.5 exposure. We used 1,581 valid observations of 36 subjects over five visits in 2 years to estimate associations of eNO with BC and PM2.5 according to generalized estimating equations with polynomial distributed-lag models, controlling for body mass index, asthma, temperature, and relative humidity. We also assessed the relative importance of BC and PM2.5 with two-pollutant models. Results: Air pollution concentrations and eNO were clearly lower during the 2008 Olympics. BC and PM2.5 concentrations averaged over 0–24 hr were strongly associated with eNO, which increased by 16.6% [95% confidence interval (CI), 14.1–19.2%] and 18.7% (95% CI, 15.0–22.5%) per interquartile range (IQR) increase in BC (4.0 μg/m3) and PM2.5 (149 μg/m3), respectively. In the two-pollutant model, estimated effects of BC were robust, but associations between PM2.5 and eNO decreased with adjustment for BC. We found that eNO was associated with IQR increases in hourly BC concentrations up to 10 hr after exposure, consistent with effects primarily in the first hours after exposure. Conclusions: Recent exposure to BC was associated with acute respiratory inflammation in schoolchildren in Beijing. Lower air pollution levels during the 2008 Olympics also were associated with reduced eNO. PMID:21642045

Two distinct patterns of seasonal variation of airborne black carbon over Tibetan Plateau

DOE Office of Scientific and Technical Information (OSTI.GOV)

Wang, Mo; Xu, Baiqing; Wang, Ninglian

Airborne black carbon (BC) mass concentrations were measured from November 2012 to June 2013 at Ranwu and Beiluhe, located in the southeastern and central Tibetan Plateau, respectively. Monthly mean BC concentrations showawinter (November–February) high (413.2 ng m $-$3) and spring (March–June) low(139.1 ng m $-$3) at Ranwu, but in contrast awinter lowand spring high at Beiluhe (204.8 and 621.6 ng m $-$3, respectively). By examining the meteorological conditions at various scales, we found that themonthly variation of airborne BC over the southeastern Tibetan Plateau (TP) was highly influenced by regional precipitation and over the hinterland by winds. Local precipitation atmore » both sites showed little impact on the seasonal variation of airborne BC concentrations. Potential BC source regions are identified using air mass backward trajectory analysis. At Ranwu, BC was dominated by the air masses from the northeastern India and Bangladesh in both winter and spring, whereas at Beiluhe it was largely contributed by air masses from the south slope of Himalayas in winter, and from the arid region in the north of the TP in spring. Thewinter and spring seasonal peak of BC in the southern TP is largely contributed by emissions from South Asia, and this seasonal variation is heavily influenced by the regional monsoon. In the northern TP, BC had high concentrations during spring and summer seasons, which is very likely associated with more efficient transport of BC over the arid regions on the north of Tibetan Plateau and in Central Asia. Airborne BC concentrations at the Ranwusampling site showed a significant diurnal cyclewith a peak shortly after sunrise followed by a decrease before noon in both winter and spring, likely shaped by local human activities and the diurnal variation of wind speed. At the Beiluhe sampling site, the diurnal variation of BC is different and less distinct.« less

Modified thermal-optical analysis using spectral absorption selectivity to distinguish black carbon from pyrolized organic carbon.

PubMed

Hadley, Odelle L; Corrigan, Craig E; Kirchstetter, Thomas W

2008-11-15

This study presents a method for analyzing the black carbon (BC) mass loading on a quartz fiber filter using a modified thermal-optical analysis method, wherein light transmitted through the sample is measured over a spectral region instead of at a single wavelength. Evolution of the spectral light transmission signal depends on the relative amounts of light-absorbing BC and char, the latter of which forms when organic carbon in the sample pyrolyzes during heating. Absorption selectivities of BC and char are found to be distinct and are used to apportion the amount of light attenuated by each component in the sample. Light attenuation is converted to mass concentration on the basis of derived mass attenuation efficiencies (MAEs) of BC and char. The fractions of attenuation due to each component are scaled by their individual MAE values and added together as the total mass of light absorbing carbon (LAC). An iterative algorithm is used to find the MAE values for both BC and char that provide the best fit to the carbon mass remaining on the filter (derived from direct measurements of thermally evolved CO2) at temperatures higher than 480 degrees C. This method was applied to measure the BC concentration in precipitation samples collected in northern California. The uncertainty in the measured BC concentration of samples that contained a high concentration of organics susceptible to char ranged from 12% to 100%, depending on the mass loading of BC on the filter. The lower detection limit for this method was approximately 0.35 microg of BC, and the uncertainty approached 20% for BC mass loading greater than 1.0 microg of BC.

Diesel vehicle and urban burning contributions to black carbon concentrations and size distributions in Tijuana, Mexico, during the Cal-Mex 2010 campaign

NASA Astrophysics Data System (ADS)

Takahama, S.; Russell, L. M.; Shores, C. A.; Marr, L. C.; Zheng, J.; Levy, M.; Zhang, R.; Castillo, E.; Rodriguez-Ventura, J. G.; Quintana, P. J. E.; Subramanian, R.; Zavala, M.; Molina, L. T.

2014-05-01

Black carbon (BC) was characterized by three complementary techniques - incandescence (single particle soot photometer, SP2, at Parque Morelos), light absorption (cavity ringdown spectrometer with integrating nephelometer, CRDS-Neph, at Parque Morelos and Aethalometers at seven locations), and volatility (volatility tandem differential mobility analyzer, V-TDMA) during the Cal-Mex 2010 campaign. SP2, CRDS-Neph, and Aethalometer measurements characterized the BC mass, and SP2 and V-TDMA measurements also quantified BC-containing particle number, from which mass-mean BC diameters were calculated. On average, the mass concentrations measured in Tijuana (1.8 ± 2.6 μg m-3 at Parque Morelos and 2.6 μg m-3 in other regions of Tijuana) were higher than in San Diego or the international border crossing (0.5 ± 0.6 μg m-3). The observed BC mass concentrations were attributable to nighttime urban burning activities and diesel vehicles, both from the local (Baja California) and transported (Southern California) diesel vehicle fleets. Comparisons of the SP2 and co-located Aethalometers indicated that the two methods measured similar variations in BC mass concentrations (correlation coefficients greater than 0.85), and the mass concentrations were similar for the BC particles identified from nighttime urban burning sources. When the BC source changed to diesel vehicle emissions, the SP2 mass concentrations were lower than the Aethalometer mass concentrations by about 50%, likely indicating a change in the mass absorption efficiency and quantification by the Aethalometers. At Parque Morelos there were up to three different-sized modes of BC mass in particles: one mode below 100 nm, one near 100 nm, and another between 200 and 300 nm. The mode between 200 and 300 nm was associated with urban burning activities that influenced the site during evening hours. When backtrajectories indicated that airmasses came from the south to the Parque Morelos site, BC mass in particles was also larger (mass median diameter of 170 nm rather than 155 nm), consistent with the higher fraction of older diesel vehicles in the Tijuana fleet compared to the vehicles found in southern California.

Light-absorbing impurities enhance glacier albedo reduction in the southeastern Tibetan plateau

NASA Astrophysics Data System (ADS)

Zhang, Yulan; Kang, Shichang; Cong, Zhiyuan; Schmale, Julia; Sprenger, Michael; Li, Chaoliu; Yang, Wei; Gao, Tanguang; Sillanpää, Mika; Li, Xiaofei; Liu, Yajun; Chen, Pengfei; Zhang, Xuelei

2017-07-01

Light-absorbing impurities (LAIs) in snow of the southeastern Tibetan Plateau (TP) and their climatic impacts are of interest not only because this region borders areas affected by the South Asian atmospheric brown clouds but also because the seasonal snow and glacier melt from this region form important headwaters of large rivers. In this study, we collected surface snow and snowpit samples from four glaciers in the southeastern TP in June 2015 to investigate the comprehensive observational data set of LAIs. Results showed that the LAI concentrations were much higher in the aged snow and granular ice than in the fresh snow and snowpits due to postdepositional processes. Impurity concentrations fluctuated across snowpits, with maximum LAI concentrations frequently occurring toward the bottom of snowpits. Based on the SNow ICe Aerosol Radiative model, the albedo simulation indicated that black carbon and dust account for approximately 20% of the albedo reduction relative to clean snow. The radiative forcing caused by black carbon and dust deposition on the glaciers were between 1.0-141 W m-2 and 1.5-120 W m-2, respectively. Black carbon (BC) played a larger role in albedo reduction and radiative forcing than dust in the study area, enhancing approximately 15% of glacier melt. Analysis based on the Fire INventory from NCAR indicated that nonbiomass-burning sources of BC played an important role in the total BC deposition, especially during the monsoon season. This study suggests that eliminating anthropogenic BC could mitigate glacier melt in the future of the southeastern TP.

Nutrient leaching in a Colombian savanna Oxisol amended with biochar.

PubMed

Major, Julie; Rondon, Marco; Molina, Diego; Riha, Susan J; Lehmann, Johannes

2012-01-01

Nutrient leaching in highly weathered tropical soils often poses a challenge for crop production. We investigated the effects of applying 20 t ha biochar (BC) to a Colombian savanna Oxisol on soil hydrology and nutrient leaching in field experiments. Measurements were made over the third and fourth years after a single BC application. Nutrient contents in the soil solution were measured under one maize and one soybean crop each year that were routinely fertilized with mineral fertilizers. Leaching by unsaturated water flux was calculated using soil solution sampled with suction cup lysimeters and water flux estimates generated by the model HYDRUS 1-D. No significant difference ( > 0.05) was observed in surface-saturated hydraulic conductivity or soil water retention curves, resulting in no relevant changes in water percolation after BC additions in the studied soils. However, due to differences in soil solution concentrations, leaching of inorganic N, Ca, Mg, and K measured up to a depth of 0.6 m increased ( < 0.05), whereas P leaching decreased, and leaching of all nutrients (except P) at a depth of 1.2 m was significantly reduced with BC application. Changes in leaching at 2.0 m depth with BC additions were about one order of magnitude lower than at other depths, except for P. Biochar applications increased soil solution concentrations and downward movement of nutrients in the root zone and decreased leaching of Ca, Mg, and Sr at 1.2 m, possibly by a combination of retention and crop nutrient uptake. Copyright © by the American Society of Agronomy, Crop Science Society of America, and Soil Science Society of America, Inc.

Trends of atmospheric black carbon concentration over the United Kingdom

NASA Astrophysics Data System (ADS)

Singh, Vikas; Ravindra, Khaiwal; Sahu, Lokesh; Sokhi, Ranjeet

2018-04-01

The continuous observations over a period of 7 years (2009-2016) available at 7 locations show declining trend of atmospheric BC in the UK. Among all the locations, the highest decrease of 8 ± 3 percent per year was observed at the Marylebone road in London. The detailed analysis performed at 21 locations during 2009-2011 shows that average annual mean atmospheric BC concentration were 0.45 ± 0.10, 1.47 ± 0.58, 1.34 ± 0.31, 1.83 ± 0.46 and 9.72 ± 0.78 μgm-3 at rural, suburban, urban background, urban centre and kerbside sites respectively. Around 1 μgm-3 of atmospheric BC could be attributed to urban emission, whereas traffic contributed up to 8 μg m-3 of atmospheric BC near busy roads. Seasonal pattern was also observed at all locations except rural and kerbside location, with maximum concentrations (1.2-4 μgm-3) in winter. Further, minimum concentrations (0.3-1.2 μgm-3) were observed in summer and similar concentrations in spring and fall. At suburban and urban background locations, similar diurnal pattern were observed with atmospheric BC concentration peaks (≈1.8 μg m-3) in the morning (around 9 a.m.) and evening (7-9 p.m.) rush hours, whereas minimum concentrations were during late night hours (peak at 5 a.m.) and the afternoon hours (peak at 2 p.m.). The urban centre values show a similar morning pattern (peak at 9 a.m.; concentration - 2.5 μgm-3) in relation to background locations but only a slight decrease in concentration in the afternoon which remained above 2 μgm-3 till midnight. It is concluded that the higher flow of traffic at urban centre locations results in higher atmospheric BC concentrations throughout the day. Comparison of weekday and weekend daily averaged atmospheric BC showed maximum concentrations on Friday, having minimum levels on Sunday. This study will help to refine the atmospheric BC emission inventories and provide data for air pollution and climate change models evaluation, which are used to formulate air pollution mitigation policies.

Reductions in indoor black carbon concentrations from improved biomass stoves in rural India.

PubMed

Patange, Omkar S; Ramanathan, Nithya; Rehman, I H; Tripathi, Sachi Nand; Misra, Amit; Kar, Abhishek; Graham, Eric; Singh, Lokendra; Bahadur, Ranjit; Ramanathan, V

2015-04-07

Deployment of improved biomass burning cookstoves is recognized as a black carbon (BC) mitigation measure that has the potential to achieve health benefits and climate cobenefits. Yet, few field based studies document BC concentration reductions (and resulting human exposure) resulting from improved stove usage. In this paper, data are presented from 277 real-world cooking sessions collected during two field studies to document the impacts on indoor BC concentrations inside village kitchens as a result of switching from traditional stoves to improved forced draft (FD) stoves. Data collection utilized new low-cost cellphone methods to monitor BC, cooking duration, and fuel consumption. A cross sectional study recorded a reduction of 36% in BC during cooking sessions. An independent paired sample study demonstrated a statistically significant reduction of 40% in 24 h BC concentrations when traditional stoves were replaced with FD stoves. Reductions observed in these field studies differ from emission factor reductions (up to 99%) observed under controlled conditions in laboratory studies. Other nonstove sources (e.g., kerosene lamps, ambient concentrations) likely offset the reductions. Health exposure studies should utilize reductions determined by field measurements inside village kitchens, in conjunction with laboratory data, to assess the health impacts of new cooking technologies.

Atmospheric black carbon in the Russian Arctic: anthropogenic inputs in comparison with average or extremal wood fires' ones

NASA Astrophysics Data System (ADS)

Vinogradova, Anna A.; Smirnov, Nikolay S.; Korotkov, Vladimir N.

2016-04-01

Model estimates of atmospheric black carbon concentrations were made for different points of the Russian Arctic. Anthropogenic BC emissions and wood fires' ones were calculated from Russian official statistics for the 2000s. We used the data of Ministry of Natural Resources and Environment of RF on anthropogenic air emissions of pollution in Russian cities and regions [1], as well as the data of Federal Forestry Agency of RF (Rosleshoz) [2] on wood fires. We considered the area within (50-72)N and (20-180)E, which covers about 94% of the Russian territory, where both anthropogenic and fire BC emissions have been arranged through grid cells (1×1) deg. Anthropogenic BC emissions are estimated as annual values based on the data for 54 regions and more than 100 cities. Total emission is estimated as (220 ± 30) Gg BC in 2010 [3], including emissions from open flares associated with gas/oil extractive industry which are about (25 ± 8) Gg/yr. We analyzed the data on wood fires (detailing crown, ground and underground fires in forests and fires on non-forest lands) with their spatial and seasonal variations during 15 years (2000-2014). Different combustion factors [4] and BC emission coefficients [5] were used in calculations for different types of burning. Russian total average annual BC emission from fires, occurring mainly in summertime, was estimated as 30 Gg with large variations (4-100 Gg/yr) from year to year. Asian territory emits about 90% of this value. We estimated anthropogenic (BC_A) and fires' (BC_F) contributions to BC air concentrations at different Russian Arctic points using the approach [6] - decadal back-trajectory analysis combined with spatial distribution of sensitivity pollution emission function (SPEF). Extraordinary atmospheric circulation causing, to a great extent, abnormally intensive fires in the middle latitudes often leads to a decrease in SPEF values for these territories. As a result, fires are not so dangerous for the whole Arctic, as it is believed. But there are distinctions at various points: Kola Peninsula - annually BC concentrations in air are not sizable and BCA prevails, but BCF prevails in summer. SE of Arkhangelsk region - annually BCA prevails, but in summer BCA is equal to BC_F, and in summer 2010 BCF was 2 times higher. Nenetsky Nature Reserve - BCF always prevails. Gydansky Nature Reserve - BCA prevails through a year, previously from oil/gas flares. Ust'-Lensky Nature Reserve - annually BC concentrations in air are not sizable, but in summer 2012 BCF prevails and is near the same as at Nenetsky Nature Reserve. The work was supported by RFBR, grants: 14-05-00059, 14-05-93089. _____________________ 1. Yearbook 2010 on Atmospheric Emissions of Pollution in Towns and Regions of Russian Federation. St.Petersburg, SRI Atmosphere, 2011. - 560 pp. [in Russian]. 2. http://www.rosleshoz.gov.ru/; http://www.aviales.ru/ 3. Vinogradova A.A. Anthropogenic Black Carbon Emissions to the Atmosphere: Surface Distribution through Russian Territory // DOI: 10.1134/S1024856015020141 4. http://www.ipcc-nggip.iges.or.jp/public/2006gl/vol4.html 5. Akagi S.K. et al. Emission factors for open and domestic biomass burning for use in atmospheric models // DOI: 10.5194/acp-11-4039-2011 6. Vinogradova A.A. Distant evaluation of atmospheric pollution influence on the remote territories // DOI:10.1134/S0001433815070099

Black Carbon Particle Number Distribution Measurements during the ATHENS-2013 Winter Campaign

NASA Astrophysics Data System (ADS)

Gkatzelis, Georgios; Papanastasiou, Dimitris; Florou, Kalliopi; Kaltsonoudis, Christos; Louvaris, Eyaggelos; Bezentakos, Spiridon; Biskos, Georgios; Pandis, Spuros

2014-05-01

Black Carbon (BC) particles emitted by anthropogenic sources play an important role both in climate change and in air quality degradation. Open burning in forests and savannas, combustion of diesel and solid fuels for cooking and heating in homes represent the majority of BC emissions. Earlier work has focused on the BC atmospheric direct radiative forcing that is mostly related to its mass concentration and optical properties of the corresponding particles. A variety of measurement techniques are used to measure the mass concentration of BC by taking advantage of its optical or physical properties. Moreover, the carbonaceous particles containing BC are also important for the indirect forcing of climate. This effect is mostly related to the number concentration of BC particles. The number distribution of BC particles especially below 100 nm is quite uncertain due to limitations of the existing measurement techniques. In this work we employed a thermodenuder-based method as an approach for the measurement of the BC number distribution. More specifically, we combined a thermodenuder (TD) operating at temperatures up to 300 ° C, with a Scanning Mobility Particle Sizer (SMPS) and a High Resolution Time of Flight Aerosol Mass Spectrometer (HR-ToF AMS). Aerosol size and composition measurements were carried out both at ambient and at elevated TD temperatures in Athens field campaign during January and February of 2013. In parallel, a Multi-Angle Absorption Photometer (MAAP) provided information about the BC mass concentration while a Hygroscopic Tandem Differential Mobility Analyzer (HTDMA) measured the mixing state and the hygroscopicity of the particles as a function of their size. These measurements were then combined to estimate the number concentration of BC particles. Our analysis focused on different periods during the study. During some of them one source dominated the carbonaceous aerosol concentration. Such periods included rush hour traffic, nighttime wood burning, clean air transported from other areas, mixed sources, etc. The number fraction remaining after heating at 300 ° C for approximately 15 s during wood burning events was 80-90%, suggesting that practically all particles contained nonvolatile material. Combining the SMPS, MAAP, AMS, and HTDMA measurements we show that most of the sampled material was BC. On the contrary, during rush hour traffic the number fraction remaining was only 50-60% suggesting that more than half of the particles did not contain BC.

Impact of Aerosols on Shortwave and Photosynthetically Active Radiation Balance over Sub-tropical Region in South Asia: Observational and Modeling Approach

NASA Astrophysics Data System (ADS)

Subba, T.; Pathak, B.

2016-12-01

The North-East Indian Region (NER) (22-30ºN, 89-98ºE) in south Asia sandwiched between two global biodiversity hotspots namely, Himalaya and Indo-Burma, assumes significance owing to its unique topography with mountains in the north, east and south and densely populated Indo Gangetic plains (IGP) towards the west resulting in complex aerosol system. Multi-year (2010-2014) concurrent measurements of aerosol properties and the shortwave radiation budget are examined over four geographically distinct stations of NER operational under Indian Space Research organization's ARFINET (Aerosol Radiative Forcing over India NETwork). An attempt has been made to lessen the ambiguity of forcing estimation by validating the radiative transfer modelled ARF with the CNR4 net radiometer measured values (r2 0.98). The Normalized Difference Vegetation Index and its dependence on the extinction of the photosynthetically active radiation (PAR) due to aerosol are assessed. The spring time enhancement of aerosols in the column has shown significant surface cooling (ARF = -48 ± 5 Wm-2) over the region, while the very high Black Carbon (BC) mass concentrations near the surface (SSA > 0.8) leads to significant atmospheric warming (ARF = +41 ± 7 Wm-2) in the shortwave range. Radiative forcing estimates reveal that the atmospheric forcing by BC could be as high as +30Wm-2 over the western part, which are significantly higher than the eastern part with a consequent heating rate of 1.5 K day-1 revealing an east-west asymmetry over NER. The impact of BC aerosols on the photosynthetic rate varies among different locations ranging from -5±2 Wm-2 to -25±3 Wm-2. Almost 70% of the total atmospheric shortwave radiative absorption is attributed to just 10% contribution of Black Carbon (BC) to total mass concentration and causes a reduction of more than 30% of PAR reaching the surface over Brahmaputra valley due to direct radiative effect. Comparison of previous and the present study shows highest surface dimming is observed in west-Asia followed by IGP and west-India. Surface radiative reduction over NER is comparable to south-India standing on the third place which is still higher than that of the Himalayan and Oceanic regions.

Impact of Plasma Surface Treatment on Bamboo Charcoal/silver Nanocomposite

NASA Astrophysics Data System (ADS)

Vignesh, K.; Vijayalakshmi, K. A.; Karthikeyan, N.

2016-10-01

Bamboo charcoal (BC) accompanied silver (Ag) nanocomposite is synthesized through sol-gel method. The produced BC/Ag nanocomposite was surface modified by air and oxygen plasma treatments. Silver ions (Ag+) will serve to improve the antibacterial activity as well as the surface area of BC. Plasma treatment has improved the surface functional groups, crystalline intensity and antibacterial activity of the prepared nanocomposite. Scanning electron microscopy (SEM) and X-ray diffraction (XRD) studies show that Ag nanoparticles have good agreement with BC and the particle size has a mean diameter of 20-40nm. We observe the carboxyl functional groups in Fourier transform infrared spectroscopy (FTIR) after the oxygen plasma treatment. Moreover surface area and adsorption were analyzed by using the Brunauer, Emmett and Teller (BET) surface area (SBET) and UV-Vis spectroscopy.

Transport of regional pollutants through a remote trans-Himalayan valley in Nepal

NASA Astrophysics Data System (ADS)

Dhungel, Shradda; Kathayat, Bhogendra; Mahata, Khadak; Panday, Arnico

2018-01-01

Anthropogenic emissions from the combustion of fossil fuels and biomass in Asia have increased in recent years. High concentrations of reactive trace gases and light-absorbing and light-scattering particles from these sources form persistent haze layers, also known as atmospheric brown clouds, over the Indo-Gangetic plains (IGP) from December through early June. Models and satellite imagery suggest that strong wind systems within deep Himalayan valleys are major pathways by which pollutants from the IGP are transported to the higher Himalaya. However, observational evidence of the transport of polluted air masses through Himalayan valleys has been lacking to date. To evaluate this pathway, we measured black carbon (BC), ozone (O3), and associated meteorological conditions within the Kali Gandaki Valley (KGV), Nepal, from January 2013 to July 2015. BC and O3 varied over both diurnal and seasonal cycles. Relative to nighttime, mean BC and O3 concentrations within the valley were higher during daytime when the up-valley flow (average velocity of 17 m s-1) dominated. BC and O3 concentrations also varied seasonally with minima during the monsoon season (July to September). Concentrations of both species subsequently increased post-monsoon and peaked during March to May. Average concentrations for O3 during the seasonally representative months of April, August, and November were 41.7, 24.5, and 29.4 ppbv, respectively, while the corresponding BC concentrations were 1.17, 0.24, and 1.01 µg m-3, respectively. Up-valley fluxes of BC were significantly greater than down-valley fluxes during all seasons. In addition, frequent episodes of BC concentrations 2-3 times higher than average persisted from several days to a week during non-monsoon months. Our observations of increases in BC concentration and fluxes in the valley, particularly during pre-monsoon, provide evidence that trans-Himalayan valleys are important conduits for transport of pollutants from the IGP to the higher Himalaya.

Impacts of Canadian and global black carbon shipping emissions on Arctic climate

NASA Astrophysics Data System (ADS)

Shrestha, R.; von Salzen, K.

2017-12-01

Shipping activities have increased across the Arctic and are projected to continue to increase in the future. In this study we compare the climate impacts of Canadian and global shipping black carbon (BC) emissions on the Arctic using the Canadian Center for Climate Modelling and Analysis Earth System Model (CanESM4.1). The model simulations are performed with and without shipping emissions at T63 (128 x 64) spectral resolution. Results indicate that shipping activities enhance BC concentrations across the area close to the shipping emissions, which causes increased absorption of solar radiation (direct effect). An impact of shipping on temperatures is simulated across the entire Arctic, with maximum warming in fall and winter seasons. Although global mean temperature changes are very similar between the two simulations, increase in Canadian BC shipping emissions cause warmer Arctic land surface temperature in summer due to the direct radiative effects of aerosol.

Progress in the preparation and application of modified biochar for improved contaminant removal from water and wastewater.

PubMed

Ahmed, Mohammad Boshir; Zhou, John L; Ngo, Huu H; Guo, Wenshan; Chen, Mengfang

2016-08-01

Modified biochar (BC) is reviewed in its preparation, functionality, applications and regeneration. The nature of precursor materials, preparatory conditions and modification methods are key factors influencing BC properties. Steam activation is unsuitable for improving BC surface functionality compared with chemical modifications. Alkali-treated BC possesses the highest surface functionality. Both alkali modified BC and nanomaterial impregnated BC composites are highly favorable for enhancing the adsorption of different contaminants from wastewater. Acidic treatment provides more oxygenated functional groups on BC surfaces. The Langmuir isotherm model provides the best fit for sorption equilibria of heavy metals and anionic contaminants, while the Freundlich isotherm model is the best fit for emerging contaminants. The pseudo 2(nd) order is the most appropriate model of sorption kinetics for all contaminants. Future research should focus on industry-scale applications and hybrid systems for contaminant removal due to scarcity of data. Copyright © 2016 Elsevier Ltd. All rights reserved.

Enhanced capture of elemental mercury by bamboo-based sorbents.

PubMed

Tan, Zengqiang; Xiang, Jun; Su, Sheng; Zeng, Hancai; Zhou, Changsong; Sun, Lushi; Hu, Song; Qiu, Jianrong

2012-11-15

To develop cost-effective sorbent for gas-phase elemental mercury removal, the bamboo charcoal (BC) produced from renewable bamboo and KI modified BC (BC-I) were used for elemental mercury removal. The effect of NO, SO2 on gas-phase Hg0 adsorption by KI modified BC was evaluated on a fixed bed reactor using an online mercury analyzer. BET surface area analysis, temperature programmed desorption (TPD) and X-ray photoelectron spectroscopy (XPS) were used to determine the pore structure and surface chemistry of the sorbents. The results show that KI impregnation reduced the sorbents' BET surface area and total pore volume compared with that of the original BC. But the BC-I has excellent adsorption capacity for elemental mercury at a relatively higher temperature of 140 °C and 180 °C. The presence of NO or SO2 could inhibit Hg0 capture, but BC-I has strong anti-poisoning ability. The specific reaction mechanism has been further analyzed. Copyright © 2012 Elsevier B.V. All rights reserved.

Influence of soil biochar aging on sorption of the herbicides MCPA, nicosulfuron, terbuthylazine, indaziflam, and fluoroethyldiaminotriazine.

PubMed

Trigo, Carmen; Spokas, Kurt A; Cox, Lucia; Koskinen, William C

2014-11-12

Sorption of four herbicides and a metabolite of indaziflam on a fresh macadamia nut biochar and biochars aged one or two years in soil was characterized. On fresh biochar, the sorption was terbuthylazine (Kd = 595) > indaziflam (Kd = 162) > MCPA (Kd = 7.5) > fluoroethyldiaminotriazine (Kd = 0.26) and nicosulfuron (Kd = 0). Biochar surface area increased with aging attributed to the loss of a surface film. This was also manifested in a decline in water extractable organic carbon with aging. Correspondingly, an increase in the aromaticity was observed. The higher surface area and porosity in aged biochar increased sorption of indaziflam (KdBC-2yr = 237) and fluoroethyldiaminotriazine (KdBC-1yr = 1.2 and KdBC-2yr = 3.0), but interestingly decreased sorption of terbuthylazine (KdBC-1yr = 312 and KdBC-2yr = 221) and MCPA (KdBC-1yr = 2 and KdBC-2yr = 2). These results will facilitate development of biochars for specific remediation purposes.

Spatiotemporal Association of Real-Time Concentrations of Black Carbon (BC) with Fine Particulate Matters (PM2.5) in Urban Hotspots of South Korea.

PubMed

Kim, Sungroul; Yu, Sol; Yun, Dongmin

2017-11-06

We evaluated the spatiotemporal distributions of black carbon (BC) and particulate matters with aerodynamic diameters of less than 2.5 m (PM 2.5 ) concentrations at urban diesel engine emission (DEE) hotspots of South Korea. Concentrations of BC and PM 2.5 were measured at the entrance gate of two diesel bus terminals and a train station, in 2014. Measurements were conducted simultaneously at the hotspot (Site 1) and at its adjacent, randomly selected, residential areas, apartment complex near major roadways, located with the same direction of 300 m (Site 2) and 500 m (Site 3) away from Site 1 on 4 different days over the season, thrice per day; morning ( n = 120 measurements for each day and site), evening ( n = 120), and noon ( n = 120). The median (interquartile range) PM 2.5 ranged from 12.6 (11.3-14.3) to 60.1 (47.0-76.0) μg/m³ while those of BC concentrations ranged from 2.6 (1.9-3.7) to 6.3 (4.2-10.3) μg/m³. We observed a strong relationship of PM 2.5 concentrations between sites (slopes 0.89-0.9, the coefficient of determination 0.89-0.96) while the relationship for BC concentrations between sites was relatively weak (slopes 0.76-0.85, the coefficient of determination 0.54-0.72). PM 2.5 concentrations were changed from 4% to 140% by unit increase of BC concentration, depending on site and time while likely supporting the necessity of monitoring of BC as well as PM 2.5 , especially at urban DEE related hotspot areas.

Granular biochar compared with activated carbon for wastewater treatment and resource recovery.

PubMed

Huggins, Tyler M; Haeger, Alexander; Biffinger, Justin C; Ren, Zhiyong Jason

2016-05-01

Granular wood-derived biochar (BC) was compared to granular activated carbon (GAC) for the treatment and nutrient recovery of real wastewater in both batch and column studies. Batch adsorption studies showed that BC material had a greater adsorption capacity at the high initial concentrations of total chemical oxygen demand (COD-T) (1200 mg L(-1)), PO4 (18 mg L(-1)), and NH4 (50 mg L(-1)) compared to GAC. Conversely the BC material showed a lower adsorption capacity for all concentrations of dissolved chemical oxygen demand (COD-D) and the lower concentrations of PO4 (5 mg L(-1)) and NH4 (10 mg L(-1)). Packed bed column studies showed similar average COD-T removal rate for BC with 0.27 ± 0.01 kg m(-3) d(-1) and GAC with 0.24 ± 0.01 kg m(-3) d(-1), but BC had nearly twice the average removal rate (0.41 ± 0.08 kg m(-3) d(-3)) compared to GAC during high COD-T concentrations (>500 mg L(-1)). Elemental analysis showed that both materials accumulated phosphorous during wastewater treatment (2.6 ± 0.4 g kg(-1) and 1.9 ± 0.1 g kg(-1) for BC and GAC respectively). They also contained high concentrations of other macronutrients (K, Ca, and Mg) and low concentrations of metals (As, Cd, Cr, Pb, Zn, and Cu). The good performance of BC is attributed to its macroporous structure compared with the microporous GAC. These favorable treatment data for high strength wastewater, coupled with additional life-cycle benefits, helps support the use of BC in packed bed column filters for enhanced wastewater treatment and nutrient recovery. Copyright © 2016 Elsevier Ltd. All rights reserved.

Measured Black Carbon Deposition on the Sierra Nevada Snow Pack and Implication for Snow Pack Retreat

DOE Office of Scientific and Technical Information (OSTI.GOV)

Hadley, O.L.; Corrigan, C.E.; Kirchstetter, T.W.

2010-01-12

Modeling studies show that the darkening of snow and ice by black carbon deposition is a major factor for the rapid disappearance of arctic sea ice, mountain glaciers and snow packs. This study provides one of the first direct measurements for the efficient removal of black carbon from the atmosphere by snow and its subsequent deposition to the snow packs of California. The early melting of the snow packs in the Sierras is one of the contributing factors to the severe water problems in California. BC concentrations in falling snow were measured at two mountain locations and in rain atmore » a coastal site. All three stations reveal large BC concentrations in precipitation, ranging from 1.7 ng/g to 12.9 ng/g. The BC concentrations in the air after the snow fall were negligible suggesting an extremely efficient removal of BC by snow. The data suggest that below cloud scavenging, rather than ice nuclei, was the dominant source of BC in the snow. A five-year comparison of BC, dust, and total fine aerosol mass concentrations at multiple sites reveals that the measurements made at the sampling sites were representative of large scale deposition in the Sierra Nevada. The relative concentration of iron and calcium in the mountain aerosol indicates that one-quarter to one-third of the BC may have been transported from Asia.« less

Stormwater and fire as sources of black carbon nanoparticles to Lake Tahoe.

PubMed

Bisiaux, Marion M; Edwards, Ross; Heyvaert, Alan C; Thomas, James M; Fitzgerald, Brian; Susfalk, Richard B; Schladow, S Geoffrey; Thaw, Melissa

2011-03-15

Emitted to the atmosphere through fire and fossil fuel combustion, refractory black carbon nanoparticles (rBC) impact human health, climate, and the carbon cycle. Eventually these particles enter aquatic environments, where they may affect the fate of other pollutants. While ubiquitous, the particles are still poorly characterized in freshwater systems. Here we present the results of a study determining rBC in waters of the Lake Tahoe watershed in the western United States from 2007 to 2009. The study period spanned a large fire within the Tahoe basin, seasonal snowmelt, and a number of storm events, which resulted in pulses of urban runoff into the lake with rBC concentrations up to 4 orders of magnitude higher than midlake concentrations. The results show that rBC pulses from both the fire and urban runoff were rapidly attenuated suggesting unexpected aggregation or degradation of the particles. We find that those processes prevent rBC concentrations from building up in the clear and oligotrophic Lake Tahoe. This rapid removal of rBC soon after entry into the lake has implications for the transport of rBC in the global aquatic environment and the flux of rBC from continents to the global ocean.

Scavenging of black carbon in mixed phase clouds at the high alpine site Jungfraujoch

NASA Astrophysics Data System (ADS)

Cozic, J.; Verheggen, B.; Mertes, S.; Connolly, P.; Bower, K.; Petzold, A.; Baltensperger, U.; Weingartner, E.

2007-04-01

The scavenging of black carbon (BC) in liquid and mixed phase clouds was investigated during intensive experiments in winter 2004, summer 2004 and winter 2005 at the high alpine research station Jungfraujoch (3580 m a.s.l., Switzerland). Aerosol residuals were sampled behind two well characterized inlets; a total inlet which collected cloud particles (droplets and ice particles) as well as interstitial (unactivated) aerosol particles; an interstitial inlet which collected only interstitial aerosol particles. BC concentrations were measured behind each of these inlets along with the submicrometer aerosol number size distribution, from which a volume concentration was derived. These measurements were complemented by in-situ measurements of cloud microphysical parameters. BC was found to be scavenged into the condensed phase to the same extent as the bulk aerosol, which suggests that BC was covered with soluble material through aging processes, rendering it more hygroscopic. The scavenged fraction of BC (FScav,BC), defined as the fraction of BC that is incorporated into cloud droplets and ice crystals, decreases with increasing cloud ice mass fraction (IMF) from FScav,BC=60% in liquid phase clouds to FScav,BC~5-10% in mixed-phase clouds with IMF>0.2. This can be explained by the evaporation of liquid droplets in the presence of ice crystals (Wegener-Bergeron-Findeisen process), releasing BC containing cloud condensation nuclei back into the interstitial phase. In liquid clouds, the scavenged BC fraction is found to decrease with decreasing cloud liquid water content. The scavenged BC fraction is also found to decrease with increasing BC mass concentration since there is an increased competition for the available water vapour.

Scavenging of black carbon in mixed phase clouds at the high alpine site Jungfraujoch

NASA Astrophysics Data System (ADS)

Cozic, J.; Verheggen, B.; Mertes, S.; Connolly, P.; Bower, K.; Petzold, A.; Baltensperger, U.; Weingartner, E.

2006-11-01

The scavenging of black carbon (BC) in liquid and mixed phase clouds was investigated during intensive experiments in winter 2004, summer 2004 and winter 2005 at the high alpine research station Jungfraujoch (3580 m a.s.l., Switzerland). Aerosol residuals were sampled behind two well characterized inlets; a total inlet which collected cloud particles (drops and ice particles) as well as interstitial aerosol particles; an interstitial inlet which collected only interstitial (unactivated) aerosol particles. BC concentrations were measured behind each of these inlets along with the submicrometer aerosol number size distribution, from which a volume concentration was derived. These measurements were complemented by in-situ measurements of cloud microphysical parameters. BC was found to be scavenged into the cloud phase to the same extent as the bulk aerosol, which suggests that BC was covered with soluble material through aging processes, rendering it more hygroscopic. The scavenged fraction of BC (FScav,BC), defined as the fraction of BC that is incorporated into cloud droplets and ice crystals, decreases with increasing cloud ice mass fraction (IMF) from FScav,BC=60% in liquid phase clouds to FScav,BC~10% in mixed-phase clouds with IMF>0.2. This is explained by the evaporation of liquid droplets in the presence of ice crystals (Wegener-Bergeron-Findeisen process), releasing BC containing cloud condensation nuclei back into the interstitial phase. In liquid clouds, the scavenged BC fraction is found to decrease with decreasing cloud liquid water content. The scavenged BC fraction is also found to decrease with increasing BC mass concentration since there is an increased competition for the available water vapour.

Aerosol black carbon at an urban site-Srinagar, Northwestern Himalaya, India: Seasonality, sources, meteorology and radiative forcing

NASA Astrophysics Data System (ADS)

Bhat, Mudasir Ahmad; Romshoo, Shakil Ahmad; Beig, Gufran

2017-09-01

Black carbon (BC) mass concentration was measured first-time at a high altitude urban site-Srinagar (1600 m asl), in northwestern Himalaya, India using an Aethalometer during 2013 to study temporal variations (monthly, diurnal and seasonal), meteorological influences, source and its radiative forcing. Diurnal variations with two peaks (at 8-10 h and 20-23 h) and two dips (at 13-17 h and 0-3 h) were observed throughout the year with varying magnitude. November and April showed the highest (13.6 μg/m3) and the lowest (3.4 μg/m3) mean monthly BC concentration respectively. Seasonally, autumn displayed the highest (9.2 μg/m3) and spring the lowest (3.5 μg/m3) mean BC concentration. Annual average BC concentration was quite higher (6 μg/m3) than those reported for other high altitude stations. Wind speed, Minimum temperature and total precipitation showed a clear negative correlation with BC (r = -0.63, -0.51 and -0.55 respectively), while as, the evening relative humidity showed positive correlation (r = 0.56). During autumn, spring and winter seasons, the main source of BC at Srinagar is the biomass burning, while during summer season, equal contribution of BC is from fossil fuel and biomass burning. Back trajectory simulations revealed that, except summer, westerly air masses are the dominant winds, transporting BC from central Asia, west Asia, south Asia, Africa and some parts of Europe to Srinagar adding to its local sources. Clear-sky short wave radiative forcing of atmosphere due to BC was highest (58.2 W m-2) during autumn which leads to the increase in lower atmospheric heating rate by 1.6 K/d. The high concentration of BC observed over the high-altitude Himalayan Kashmir region has serious implications for the regional climate, hydrology and cryosphere which needs to be investigated.

Development of a portable wireless system for bipolar concentric ECG recording

NASA Astrophysics Data System (ADS)

Prats-Boluda, G.; Ye-Lin, Y.; Bueno Barrachina, J. M.; Senent, E.; Rodriguez de Sanabria, R.; Garcia-Casado, J.

2015-07-01

Cardiovascular diseases (CVDs) remain the biggest cause of deaths worldwide. ECG monitoring is a key tool for early diagnosis of CVDs. Conventional monitors use monopolar electrodes resulting in poor spatial resolution surface recordings and requiring extensive wiring. High-spatial resolution surface electrocardiographic recordings provide valuable information for the diagnosis of a wide range of cardiac abnormalities, including infarction and arrhythmia. The aim of this work was to develop and test a wireless recording system for acquiring high spatial resolution ECG signals, based on a flexible tripolar concentric electrode (TCE) without cable wiring or external reference electrode which would make more comnfortable its use in clinical practice. For this, a portable, wireless sensor node for analogue conditioning, digitalization and transmission of a bipolar concentric ECG signal (BC-ECG) using a TCE and a Mason-likar Lead-I ECG (ML-Lead-I ECG) signal was developed. Experimental results from a total of 32 healthy volunteers showed that the ECG fiducial points in the BC-ECG signals, recorded with external and internal reference electrode, are consistent with those of simultaneous ML-Lead-I ECG. No statistically significant difference was found in either signal amplitude or morphology, regardless of the reference electrode used, being the signal-to-noise similar to that of ML-Lead-I ECG. Furthermore, it has been observed that BC-ECG signals contain information that could not available in conventional records, specially related to atria activity. The proposed wireless sensor node provides non-invasive high-local resolution ECG signals using only a TCE without additional wiring, which would have great potential in medical diagnosis of diseases such as atrial or ventricular fibrillations or arrhythmias that currently require invasive diagnostic procedures (catheterization).

Dissolved black carbon in the global cryosphere: concentrations and chemical signatures

NASA Astrophysics Data System (ADS)

Khan, A. L.; Wagner, S.; Jaffe, R.; Xian, P.; Williams, M. W.; Armstrong, R. L.; McKnight, D. M.

2017-12-01

Black carbon (BC) is derived from the incomplete combustion of biomass and fossil fuels and can enhance glacial recession when deposited on snow and ice surfaces. Here we explore the influence of environmental conditions and the proximity to anthropogenic sources on the concentration and composition of dissolved black carbon (DBC), as measured by benzenepolycaroxylic acid (BPCA) markers, across snow, lakes, and streams from the global cryosphere. Data are presented from Antarctica, the Arctic, and high alpine regions of the Himalayas, Rockies, Andes, and Alps. DBC concentrations spanned from 0.62 μg/L to 170 μg/L. The median and (2.5, 97.5) quantiles in the pristine samples were 1.8 μg/L (0.62, 12), and non-pristine samples were 21 μg/L (1.6, 170). DBC is susceptible to photodegradation when exposed to solar radiation. This process leads to a less condensed BPCA signature. In general, DBC across the dataset was comprised of less-polycondensed DBC. However, DBC from the Greenland Ice Sheet (GRIS) had a highly-condensed BPCA molecular signature. This could be due to recent deposition of BC from Canadian wildfires. Variation in DBC appears to be driven by a combination of photochemical processing and the source combustion conditions under which the DBC was formed. Overall, DBC was found to persist across the global cryosphere in both pristine and non-pristine snow and surface waters. The high concentration of DBC measured in supra-glacial melt on the GRIS suggests DBC can be mobilized across ice surfaces. This is significant because these processes may jointly exacerbate surface albedo reduction in the cryosphere.

Optimization of ultrasonic-assisted extraction of bioactive alkaloid compounds from rhizoma coptidis (Coptis chinensis Franch.) using response surface methodology.

PubMed

Teng, Hui; Choi, Yong Hee

2014-01-01

The optimum extraction conditions for the maximum recovery of total alkaloid content (TAC), berberine content (BC), palmatine content (PC), and the highest antioxidant capacity (AC) from rhizoma coptidis subjected to ultrasonic-assisted extraction (UAE) were determined using response surface methodology (RSM). Central composite design (CCD) with three variables and five levels was employed, and response surface plots were constructed in accordance with a second order polynomial model. Analysis of variance (ANOVA) showed that the quadratic model was well fitted and significant for responses of TAC, BC, PC, and AA. The optimum conditions obtained through the overlapped contour plot were as follows: ethanol concentration of 59%, extraction time of 46.57min, and temperature of 66.22°C. Verification experiment was carried out, and no significant difference was found between observed and estimated values for each response, suggesting that the estimated models were reliable and valid for UAE of alkaloids. Crown Copyright © 2013. Published by Elsevier Ltd. All rights reserved.

Simulations of aerosol constituents and their sources of origin over Indo-Gangetic plain (IGP) to Himalayan foothills: a new perspective of GCM estimates

NASA Astrophysics Data System (ADS)

Kumar, B. D.; Verma, S.; Wang, R.; Boucher, O.

2016-12-01

In the present study, we evaluated aerosol constituents of the model using the measurements during premonsoon over Indo-Gangetic plain (IGP) to Himalayan foothills. Aerosol transport simulations were carried out in general circulation model (GCM) of Laboratoire de M ´et ´eorologie Dynamique (LMD-GCM) with three set of emissions including Indian emissions in GCM-Indemiss, global emissions in GCM coupled with aerosol interactive chemistry (GCM-INCA-I), and the global emissions with updated BC emission inventory over Asia in GCM-INCA-II. Among three models, GCM-indemiss reproduced measured single scattering albedo (SSA) at 670 nm with a relative bias of 5%. However, the estimated 30-50% of the measured aerosol optical depth (AOD) at 550 nm and 20-60% of the measured surface concentration of aerosol constituents (e.g. black carbon (BC), organic carbon (OC), and sulfate) at most of the times over the study period. Inability of model to reproduce observed AOD changes was attributed to the paucity of emissions represented in the model. Design of retrieval simulations using existing GCM-indemiss estimates was further carried out. Retrieval simulations have produced better results, which showed constituent surface concentration in the vicinity of the measurements with normalized mean bias (NMB) of <30%. Scatter analysis between surface and elevated contribution of region's emissions showed anthropogenic emissions from the IGP on anthropogenic days and the north west India (NWI) on anthropogenic with dust days influence aerosols over northern India (NI). Our analysis showed BC emissions from base inventory for the corresponding grids of source region influencing NI were lower by 200% compared to that of modified scenario. These emissions will further be implemented in an atmospheric GCM to evaluate their performance validating with measurements data.

Spatial and temporal variations in traffic-related particulate matter at New York City high schools

NASA Astrophysics Data System (ADS)

Patel, Molini M.; Chillrud, Steven N.; Correa, Juan C.; Feinberg, Marian; Hazi, Yair; Deepti, K. C.; Prakash, Swati; Ross, James M.; Levy, Diane; Kinney, Patrick L.

Relatively little is known about exposures to traffic-related particulate matter at schools located in dense urban areas. The purpose of this study was to examine the influences of diesel traffic proximity and intensity on ambient concentrations of fine particulate matter (PM 2.5) and black carbon (BC), an indicator of diesel exhaust particles, at New York City (NYC) high schools. Outdoor PM 2.5 and BC were monitored continuously for 4-6 weeks at each of 3 NYC schools and 1 suburban school located 40 km upwind of the city. Traffic count data were obtained using an automated traffic counter or video camera. BC concentrations were 2-3 fold higher at urban schools compared with the suburban school, and among the 3 urban schools, BC concentrations were higher at schools located adjacent to highways. PM 2.5 concentrations were significantly higher at urban schools than at the suburban school, but concentrations did not vary significantly among urban schools. Both hourly average counts of trucks and buses and meteorological factors such as wind direction, wind speed, and humidity were significantly associated with hourly average ambient BC and PM 2.5 concentrations in multivariate regression models. An increase of 443 trucks/buses per hour was associated with a 0.62 μg/m 3 increase in hourly average BC at an NYC school located adjacent to a major interstate highway. Car traffic counts were not associated with BC. The results suggest that local diesel vehicle traffic may be important sources of airborne fine particles in dense urban areas and consequently may contribute to local variations in PM 2.5 concentrations. In urban areas with higher levels of diesel traffic, local, neighborhood-scale monitoring of pollutants such as BC, which compared to PM 2.5, is a more specific indicator of diesel exhaust particles, may more accurately represent population exposures.

Diurnal and seasonal variations of black carbon and PM2.5 over New Delhi, India: Influence of meteorology

NASA Astrophysics Data System (ADS)

Tiwari, S.; Srivastava, A. K.; Bisht, D. S.; Parmita, P.; Srivastava, Manoj K.; Attri, S. D.

2013-05-01

Black carbon (BC), which is one of the highly absorbing capacities of solar radiation, reduces albedo of atmospheric aerosol. BC along with fine particulate matters (PM2.5), which play crucial role in climate and health, was monitored online for an entire year of 2011 at an urban megacity of Delhi, situated in the northern part of India. Daily mass concentration of BC varies from 0.9 to 25.5 μg m- 3, with an annual mean of 6.7 ± 5.7 μg m- 3 displayed clear monsoon minima and winter maxima; however, PM2.5 concentration was ranging from 54.3 to 338.7 μg m- 3, with an annual mean of 122.3 ± 90.7 μg m- 3. BC typically peaked between 0800 and 1000 LST and again between 2100 and 2300 LST, corresponding to the morning and evening traffic combined with the ambient meteorological effect. During summer and monsoon, the BC concentrations were found less than 5 μg m- 3; however, the highest concentrations occurred during winter in segments from < 5 to > 10 μg m- 3. In over all study, the BC mass concentration was accounted for ~ 6% of the total PM2.5 mass, with a range from 1.0% to 14.3%. The relationship between meteorological parameters and BC mass concentrations was studied and a clear inverse relationship (r = - 0.53) between BC and wind speed was observed. Relation between visibility and BC mass concentrations was also significantly negative (- 0.81), having relatively higher correlation during post-monsoon (- 0.85) and winter (- 0.78) periods and lower during summer (- 0.45) and monsoon (- 0.54) periods. The mixed layer depths (MLDs) were found to be shallower during post monsoon (379 m) and winter (335 m) as compared during summer (1023 m) and monsoon (603 m). The study indicated that during post-monsoon season, the impact of biomass burning is higher as compared to combustion of fossil fuels. Results are well associated with the rapid growth of anthropogenic emissions and ambient meteorological conditions over the station.

Ambient measurements and source apportionment of fossil fuel and biomass burning black carbon in Ontario

NASA Astrophysics Data System (ADS)

Healy, R. M.; Sofowote, U.; Su, Y.; Debosz, J.; Noble, M.; Jeong, C.-H.; Wang, J. M.; Hilker, N.; Evans, G. J.; Doerksen, G.; Jones, K.; Munoz, A.

2017-07-01

Black carbon (BC) is of significant interest from a human exposure perspective but also due to its impacts as a short-lived climate pollutant. In this study, sources of BC influencing air quality in Ontario, Canada were investigated using nine concurrent Aethalometer datasets collected between June 2015 and May 2016. The sampling sites represent a mix of background and near-road locations. An optical model was used to estimate the relative contributions of fossil fuel combustion and biomass burning to ambient concentrations of BC at every site. The highest annual mean BC concentration was observed at a Toronto highway site, where vehicular traffic was found to be the dominant source. Fossil fuel combustion was the dominant contributor to ambient BC at all sites in every season, while the highest seasonal biomass burning mass contribution (35%) was observed in the winter at a background site with minimal traffic contributions. The mass absorption cross-section of BC was also investigated at two sites, where concurrent thermal/optical elemental carbon data were available, and was found to be similar at both locations. These results are expected to be useful for comparing the optical properties of BC at other near-road environments globally. A strong seasonal dependence was observed for fossil fuel BC at every Ontario site, with mean summer mass concentrations higher than their respective mean winter mass concentrations by up to a factor of two. An increased influence from transboundary fossil fuel BC emissions originating in Michigan, Ohio, Pennsylvania and New York was identified for the summer months. The findings reported here indicate that BC should not be considered as an exclusively local pollutant in future air quality policy decisions. The highest seasonal difference was observed at the highway site, however, suggesting that changes in fuel composition may also play an important role in the seasonality of BC mass concentrations in the near-road environment. This finding has implications for future policies aiming to improve air quality in urban environments where fuel composition changes as a function of season.

N-doping effectively enhances the adsorption capacity of biochar for heavy metal ions from aqueous solution.

PubMed

Yu, Wenchao; Lian, Fei; Cui, Guannan; Liu, Zhongqi

2018-02-01

N-doping was successfully employed to improve the adsorption capacity of biochar (BC) for Cu 2+ and Cd 2+ by direct annealing of crop straws in NH 3 . The surface N content of BC increased more than 20 times by N-doping; meanwhile the content of oxidized-N was gradually diminished but graphitic-N was formed and increased with increasing annealing temperature and duration time. After N-doping, a high graphitic-N percentage (46.4%) and S BET (418.7 m 2 /g) can be achieved for BC. As a result, the N-doped BC exhibited an excellent adsorption capacity for Cu 2+ (1.63 mmol g -1 ) and Cd 2+ (1.76 mmol g -1 ), which was up to 4.0 times higher than that of the original BC. Furthermore, the adsorption performance of the N-doped BC remained stable even at acidic conditions. A positive correlation can be found between adsorption capacity with the graphitic N content on BC surface. The surface chemistry of N-doped BC before and after the heavy metal ions adsorption was carefully examined by XPS and FTIR techniques, which indicated that the adsorption mechanisms mainly included cation-π bonding and complexation with graphitic-N and hydroxyl groups of carbon surfaces. Copyright © 2017 Elsevier Ltd. All rights reserved.

Light Absorption in Arctic Sea Ice - Black Carbon vs Chlorophyll

NASA Astrophysics Data System (ADS)

Ogunro, O. O.; Wingenter, O. W.; Elliott, S.; Hunke, E. C.; Flanner, M.; Wang, H.; Dubey, M. K.; Jeffery, N.

2015-12-01

The fingerprint of climate change is more obvious in the Arctic than any other place on Earth. This is not only because the surface temperature there has increased at twice the rate of global mean temperature but also because Arctic sea ice extent has reached a record low of 49% reduction relative to the 1979-2000 climatology. Radiation absorption through black carbon (BC) deposited on Arctic snow and sea ice surface is one of the major hypothesized contributors to the decline. However, we note that chlorophyll-a absorption owing to increasing biology activity in this region could be a major competitor during boreal spring. Modeling of sea-ice physical and biological processes together with experiments and field observations promise rapid progress in the quality of Arctic ice predictions. Here we develop a dynamic ice system module to investigate discrete absorption of both BC and chlorophyll in the Arctic, using BC deposition fields from version 5 of Community Atmosphere Model (CAM5) and vertically distributed layers of chlorophyll concentrations from Sea Ice Model (CICE). To this point, our black carbon mixing ratios compare well with available in situ data. Both results are in the same order of magnitude. Estimates from our calculations show that sea ice and snow around the Canadian Arctic Archipelago and Baffin Bay has the least black carbon absorption while values at the ice-ocean perimeter in the region of the Barents Sea peak significantly. With regard to pigment concentrations, high amounts of chlorophyll are produced in Arctic sea ice by the bottom microbial community, and also within the columnar pack wherever substantial biological activity takes place in the presence of moderate light. We show that the percentage of photons absorbed by chlorophyll in the spring is comparable to the amount attributed to BC, especially in areas where the total deposition rates are decreasing with time on interannual timescale. We expect a continuous increase in chlorophyll absorption as the biological activity becomes stronger in thin ice toward the center of the Arctic basin. Alternatively, a shift in relative importance could occur as total BC mixing ratios are reduced because of environmental advocacy.

Black Carbon Trends over Several Decades at Multiple Locations

NASA Astrophysics Data System (ADS)

Preble, C. V.; Hadley, O. L.; Bond, T. C.; Kirchstetter, T.

2012-12-01

Archived air quality data in the U.S. and Europe can be used to reconstruct past trends in black carbon (BC), an indicator of fossil fuel combustion and biomass burning. Here, we consider coefficient of haze (COH) data that was extensively measured in California, New Jersey, and other North American locations from the mid-1960s to the turn of the century. We reinstated COH monitors alongside aethalometers in Vallejo and San Jose, California, and after two years of air monitoring determined that COH is proportional to and, thus, can be used to infer past concentrations of BC. Analyzing COH data sets, we found that BC concentrations markedly decreased from 1965 to 2000 in both California and New Jersey. The opposing trend of increasing energy consumption over the same period indicates successful regulatory control of sources and a shift from dirtier to cleaner fuels. As air quality improved over four decades, a seasonal trend of maximum BC concentrations in winter persisted in California but, somewhat surprisingly, disappeared in New Jersey. A strong weekly cycle of lowest BC concentrations on weekends was evident in California and New Jersey, suggesting that diesel traffic, which exhibits a similar weekly cycle, has been a major source of BC in both states. Our extended analysis will include BC trends in other regions of North America and Europe and will be applied to understand BC radiative forcing in California and deposition of pollutants in the Arctic.

Assessing the chemical and biological accessibility of the herbicide isoproturon in soil amended with biochar.

PubMed

Sopeña, Fatima; Semple, Kirk; Sohi, Saran; Bending, Gary

2012-06-01

There is considerable current interest in using biochar (BC) as a soil amendment to sequester carbon to mitigate climate change. However, the implications of adding BC to agricultural soil for the environmental fate of pesticides remain unclear. In particular, the effect of biochars on desorption behavior of compounds is poorly understood. This study examined the influence of BC on pesticide chemical and biological accessibility using the herbicide isoproturon (IPU). Soils amended with 1% and 2% BC showed enhanced sorption, slower desorption, and reduced biodegradation of IPU. Addition of 0.1% BC had no effect on sorption, desorption or biodegradation of IPU. However, the mineralization of (14)C-IPU was reduced by all BC concentrations, reducing by 13.6%, 40.1% and 49.8% at BC concentrations of 0.1%, 1% and 2% respectively. Further, the ratio of the toxic metabolite 4-isopropyl-aniline to intact IPU was substantially reduced by higher BC concentrations. Hydroxypropyl-β-cyclodextrin (HPCD) extractions were used to estimate the IPU bioaccessibility in the BC-amended soil. Significant correlations were found between HPCD-extracted (14)C-IPU and the IPU desorbed (%) (r(2)=0.8518, p<0.01), and also the (14)C-IPU mineralized (%) (r(2)=0.733; p<0.01) for all BC-amended soils. This study clearly demonstrates how desorption in the presence of BC is intimately related to pesticide biodegradation by the indigenous soil microbiota. BC application to agricultural soils can affect the persistence of pesticides as well as the fate of their degradation products. This has important implications for the effectiveness of pesticides as well as the sequestration of contaminants in soils. Copyright © 2012 Elsevier Ltd. All rights reserved.

Impacts of Himalayas on black carbon over the Tibetan Plateau during summer monsoon.

PubMed

Zhao, Shuyu; Tie, Xuexi; Long, Xin; Cao, Junji

2017-11-15

The Tibetan Plateau (TP) plays important roles in global climate and environment. This study combines in-situ BC measurements in the Himalayas and the Indo-Gangetic Plain (IGP) with a regional dynamical and chemical model (WRF-Chem model) to investigate the effect of the trans-Himalayas on black carbon (BC) from the IGP to the TP during Indian summer monsoon. To determine topographic effects of the trans-Himalayas on BC concentrations over the TP, sensitive experiments were conducted by applying the WRF-Chem model. The results showed that the reduction of the altitude of the Himalayas had an important effect on the trans-Himalayas transport of BC. There was an obvious increase in BC concentration over the trans-Himalayas region, but no significant increase over the TP because the TP (a.m.s.l ~4km) always acted as a wall to prevent BC transport from the IGP to the TP. The trans-Himalayas transport of BC was strongly dependent upon meteorological conditions over the IGP. During summer monsoon, there were three types of cyclones at different locations and one kind of convergent circulation in the IGP. Under the condition of convergent airflows, a strong northeastward wind produced the trans-Himalayas transport of BC. As a result, BC concentrations in the southeastern TP significantly increased to 0.6-0.8μgm -3 . When the cyclone located in the eastern IGP, high BC concentrations over the IGP were transported along the foothill of the Himalayas, resulting in a significant reduction of the trans-Himalayas transport. When the cyclone moved to the west, the dynamical perturbations for the trans-Himalayas transport were weaker than the eastern cyclone, and the trans-Himalayas transport were enhanced in the middle and eastern Himalayas. This study will be helpful to assess the impacts of BC particles emitted from South Asia on regional climate change and ecological environment over the TP in the future. Copyright © 2017 Elsevier B.V. All rights reserved.

Resistance to quaternary ammonium compounds in food-related bacteria.

PubMed

Sidhu, Maan Singh; Sørum, Henning; Holck, Askild

2002-01-01

Microbial resistance to antimicrobial agents continues to be a major problem. The frequent use and misuse of disinfectants based on quaternary ammonium compounds (QACs) in food-processing industries have imposed a selective pressure and may contribute to the emergence of disinfectant-resistant microorganisms. A total number of 1,325 Gram-negative isolates (Escherichia coli, other coliforms Vibrio spp., and Aeromonas spp.) and 500 Enterococcus spp. from food and food-processing industries and fish farming were screened for natural resistance to the QAC-based disinfectant benzalkonium chloride (BC). Of the 1,825 isolates, 16 strains, mainly from meat retail shops, showed low-level resistance to BC. None of the Enterococcus spp. from broiler, cattle, and pigs, the antibiotic-resistant E. coli from pig intestine and fish pathogens Vibrio spp. and Aeromonas spp. from the Norwegian fish farming industry were resistant to BC. The BC-resistant strains were examined for susceptibility to 15 different antibiotics, disinfectants, and dyes. No systematic cross-resistance between BC and any of the other antimicrobial agents tested was detected. Stable enhanced resistance in Enterobacter cloacae isolates was demonstrated by step-wise adaptation in increasing concentrations of BC. In conclusion, BC resistance among food-associated Gram-negative bacteria and Enterococcus spp. is not frequent, but resistance may develop to user concentrations after exposure to sublethal concentrations of BC.

Wet Removal of Organic and Black Carbon Aerosols

NASA Astrophysics Data System (ADS)

Torres, A.; Bond, T. C.; Lehmann, C.

2012-12-01

Organic carbon (OC) and black carbon (BC) aerosols derived from the combustion of fossil fuels and biomass are significant atmospheric pollutants that alter the Earth's radiation balance and affect human health. Carbonaceous aerosol lifetime and extent of its effects are mainly controlled by its wet removal, especially by rain. Limited work has been done to measure both BC and OC from rain events even though these aerosols are co-emitted and exist together in the atmosphere. The choices of analytical techniques for measuring OC and BC in water are limited, and researchers often employ the same techniques used for measuring atmospheric carbon particles. There is no agreement in the methods employed for monitoring carbon concentration in precipitation. As part of the method development, the Single Particle Soot Photometer (SP2), Thermal-Optical Analysis (TOA), Ultraviolet/Visible (UV/VIS) Spectrophotometer, and the Total Organic Carbon (TOC) Analyzer were evaluated for measuring BC suspended in water, water insoluble OC (WIOC) and dissolved OC (DOC). The study also monitored the concentration of BC, WIOC, and DOC in rainwater collected at Bondville (Illinois) for 18 months. Results indicated that 34% (±3%) of the BC mass was lost in the SP2 analysis, most probably during the nebulization process. Filtration required for TOA also had large losses (>75%) because quartz fiber filters were ineffective for capturing BC particles from water. Addition of NH4H2PO4 as a coagulant improved (>95%) the capture efficiency of the filters. UV/VIS spectrophotometry had good linearity, but the sensitivity for detecting BC particles (±20 μg/L) suspended in water was inadequate. TOC analysis was a robust technique for measuring both DOC and total carbon (BC + OC). The chosen techniques were TOC analysis for DOC, and TOA with an optimized filtration procedure for BC and WIOC. The mean concentrations in rainwater were 8.72 (±9.84) μg/L of BC, 88.97 (±62.64) μg/L of WIOC, and 1,320 (1,380) μg/L of DOC. DOC contributed, mostly with anions, to the ion balance of rain samples. The total carbon concentration (BC+WIOC+DOC) decreased with increasing precipitation volume and directly correlated with the concentrations of SO42-, NO3-, Ca2+, NH4+, Mg2+, and K+ in rainwater.

Linking Atmospheric Pollution to Cryospheric Changes over the Third Pole

NASA Astrophysics Data System (ADS)

Kang, S.; Zhang, Q.; Ji, Z.; Li, Y.; Chen, J.; Zhang, G.; Li, C.; Cong, Z.; Chen, P.; Guo, J.; Huang, J.; Tripathee, L.; Rupakheti, D.; Li, X.; Zhang, Y.; Panday, A. K.; Rupakheti, M.

2016-12-01

Known as "the Third Pole" (TP), the Tibetan Plateau and surrounding mountains hold the largest aggregate of glaciers outside the pole regions. Recent monitoring and projection indicated an accelerated glacier decline and increasing glacier runoff. The long-range transport of South Asian atmospheric pollutants, including light absorbing impurities (LAIs) such as black carbon (BC) and mineral dust (MD), can absorb the solar radiation in the atmosphere and reduce albedo after being deposited onto the cryosphere, thereby promoting glacier and snow melt. A coordinated atmospheric pollution monitoring network has been launched covering the TP with emphasis on trans-Himalayan transects since 2013. TSP were collected for 24h at an interval of 3-6 days. BC/OC, polycyclic aromatic hydrocarbons (PAHs) and heavy metals were measured. Results reveal a consistent decrease in almost all analyzed parameters from south to north across the Himalayas. Geochemical signatures of carbonaceous aerosols indicate dominant sources of biomass burning and vehicle exhaust, in line with results of PAHs. Integrated analysis of satellite images and air mass trajectories suggest that the trans-boundary air pollution occurred episodically and concentrated in pre-monsoon seasons via upper air circulation, through-valley wind, and local convection. Simulation results showed that carbonaceous aerosols produced positive/negative shortwave radiative forcing in the atmosphere/ground surface. Aerosols increased surface air temperatures by 0.1-0.5° over the TP and decreased temperatures in South Asia during the monsoon season. Surface snow/ice samples were collected from benchmark glaciers to estimate the impacts of LAIs on glacier melt with model assistance. BC (37%) and MD (32%) contribute to the summer melting of Laohugou Glacier in the northern TP. MD (38%) contributed more glacier melt than BC (11%) on Zhadang Glacier in the southern TP. In the southeastern TP, BC and MD contribute to 30% of the total glacier melt, up to 350 mm w.e. yr-1. The monitoring network and ongoing studies point to trans-boundary pollution as an increasing stressor for the TP environment, and highlighted the link between atmospheric pollution and cryospheric changes as well as other surface ecosystems over high mountain regions.

Emissions of Black Carbon Particles in Anthropogenic and Biomass Plumes over California during CARB 2008

NASA Astrophysics Data System (ADS)

Sahu, L. K.; Kondo, Y.; Moteki, N.; Takegawa, N.; Zhao, Y.; Vay, S. A.; Diskin, G. S.; Wisthaler, A.; Huey, L. G.

2009-12-01

Measurements of black carbon (BC) and other chemical species were made from the NASA DC-8 aircraft during the CARB campaign conducted over California in June 2008. We operated an SP2 system that measured BC and scattering particles. The vertical profiles of BC and scattering particles show enhancements in the lower troposphere. We have used relations of CO-CH3CN-SO2 to identify the sources of major plumes. The plumes originating from anthropogenic activities, mainly due to the use of fossil fuels (FF), were observed near the surface. However, the influence of smoke plumes from wild fire or biomass-burning (BB) sources was observed up to 3 km. Overall, the 1-minute average BC mass concentrations were in the ranges of about 90-500 ng/m3 and 300-700 ng/m3 in FF and BB plumes, respectively. The shell/core diameter ratios were much lagerer in BB plumes than those in FF plumes. Namely, the median shell/core ratios were 1.2-1.4 for FF plumes, while they were 1.4-1.7 for BB plumes. In both FF and BB plumes, the mass-size distributions of BC were single mode lognormal. However, the mass median diameters FF plumes were considerably smaller. The BC-CO2 regression slopes were 19±9 ng m-3/ppmv and 270±90 ng m-3/ppmv for FF and BB plumes, respectively. On the other hand the regression slopes of BC-CO were about 3.3 ng m-3/ppbv in both the plumes. Conversely, the regression slopes of BC with other co-emitted combustions products can be used to estimate the contributions of emissions from different sources.

Using Combustion Tracers to Estimate Surface Black Carbon Distributions in WRF-Chem

NASA Astrophysics Data System (ADS)

Raman, A.; Arellano, A. F.

2015-12-01

Black Carbon (BC) emissions significantly affect the global and regional climate, air quality, and human health. However, BC observations are currently limited in space and time; leading to considerable uncertainties in the estimates of BC distribution from regional and global models. Here, we investigate the usefulness of carbon monoxide (CO) in quantifying BC across continental United States (CONUS). We use high resolution EPA AQS observations of CO and IMPROVE BC to estimate BC/CO ratios. We model the BC and CO distribution using the community Weather Research and Forecasting model with Chemistry (WRF-Chem). We configured WRF-Chem using MOZART chemistry, NEI 2005, MEGAN, and FINNv1.5 for anthropogenic, biogenic and fire emissions, respectively. In this work, we address the following three key questions: 1) What are the discrepancies in the estimates of BC and CO distributions across CONUS during summer and winter periods?, 2) How do BC/CO ratios change for different spatial and temporal regimes?, 3) Can we get better estimates of BC from WRF-Chem if we use BC/CO ratios along with optimizing CO concentrations? We compare ratios derived from the model and observations and develop characteristic ratios for several geographical and temporal regimes. We use an independent set of measurements of BC and CO to evaluate these ratios. Finally, we use a Bayesian synthesis inversion to optimize CO from WRF-Chem using regionally tagged CO tracers. We multiply the characteristic ratios we derived with the optimized CO to obtain BC distributions. Our initial results suggest that the maximum ratios of BC versus CO occur in the western US during the summer (average: 4 ng/m3/ppbv) and in the southeast during the winter (average: 5 ng/m3/ppbv). However, we find that these relationships vary in space and time and are highly dependent on fuel usage and meteorology. We find that optimizing CO using EPA-AQS provides improvements in BC but only over areas where BC/CO ratios are close to observed values.Black Carbon (BC) emissions significantly affect the global and regional climate, air quality, and human health. However, BC observations are currently limited in space and time; leading to considerable uncertainties in the estimates of BC distribution from regional and global models. Here, we investigate the usefulness of carbon monoxide (CO) in quantifying BC across continental United States (CONUS). We use high resolution EPA AQS observations of CO and IMPROVE BC to estimate BC/CO ratios. We model the BC and CO distribution using the community Weather Research and Forecasting model with Chemistry (WRF-Chem). We configured WRF-Chem using MOZART chemistry, NEI 2005, MEGAN, and FINNv1.5 for anthropogenic, biogenic and fire emissions, respectively. In this work, we address the following three key questions: 1) What are the discrepancies in the estimates of BC and CO distributions across CONUS during summer and winter periods?, 2) How do BC/CO ratios change for different spatial and temporal regimes?, 3) Can we get better estimates of BC from WRF-Chem if we use BC/CO ratios along with optimizing CO concentrations? We compare ratios derived from the model and observations and develop characteristic ratios for several geographical and temporal regimes. We use an independent set of measurements of BC and CO to evaluate these ratios. Finally, we use a Bayesian synthesis inversion to optimize CO from WRF-Chem using regionally tagged CO tracers. We multiply the characteristic ratios we derived with the optimized CO to obtain BC distributions. Our initial results suggest that the maximum ratios of BC versus CO occur in the western US during the summer (average: 4 ng/m3/ppbv) and in the southeast during the winter (average: 5 ng/m3/ppbv). However, we find that these relationships vary in space and time and are highly dependent on fuel usage and meteorology. We find that optimizing CO using EPA-AQS provides improvements in BC but only over areas where BC/CO ratios are close to observed values.

Analysis of air pollution over Hanoi, Vietnam using multi-satellite and MERRA reanalysis datasets.

PubMed

Lasko, Kristofer; Vadrevu, Krishna Prasad; Nguyen, Thanh Thi Nhat

2018-01-01

Air pollution is one of the major environmental concerns in Vietnam. In this study, we assess the current status of air pollution over Hanoi, Vietnam using multiple different satellite datasets and weather information, and assess the potential to capture rice residue burning emissions with satellite data in a cloud-covered region. We used a timeseries of Ozone Monitoring Instrument (OMI) Ultraviolet Aerosol Index (UVAI) satellite data to characterize absorbing aerosols related to biomass burning. We also tested a timeseries of 3-hourly MERRA-2 reanalysis Black Carbon (BC) concentration data for 5 years from 2012-2016 and explored pollution trends over time. We then used MODIS active fires, and synoptic wind patterns to attribute variability in Hanoi pollution to different sources. Because Hanoi is within the Red River Delta where rice residue burning is prominent, we explored trends to see if the residue burning signal is evident in the UVAI or BC data. Further, as the region experiences monsoon-influenced rainfall patterns, we adjusted the BC data based on daily rainfall amounts. Results indicated forest biomass burning from Northwest Vietnam and Laos impacts Hanoi air quality during the peak UVAI months of March and April. Whereas, during local rice residue burning months of June and October, no increase in UVAI is observed, with slight BC increase in October only. During the peak BC months of December and January, wind patterns indicated pollutant transport from southern China megacity areas. Results also indicated severe pollution episodes during December 2013 and January 2014. We observed significantly higher BC concentrations during nighttime than daytime with peaks generally between 2130 and 0030 local time. Our results highlight the need for better air pollution monitoring systems to capture episodic pollution events and their surface-level impacts, such as rice residue burning in cloud-prone regions in general and Hanoi, Vietnam in particular.

Analysis of air pollution over Hanoi, Vietnam using multi-satellite and MERRA reanalysis datasets

PubMed Central

Vadrevu, Krishna Prasad; Nguyen, Thanh Thi Nhat

2018-01-01

Air pollution is one of the major environmental concerns in Vietnam. In this study, we assess the current status of air pollution over Hanoi, Vietnam using multiple different satellite datasets and weather information, and assess the potential to capture rice residue burning emissions with satellite data in a cloud-covered region. We used a timeseries of Ozone Monitoring Instrument (OMI) Ultraviolet Aerosol Index (UVAI) satellite data to characterize absorbing aerosols related to biomass burning. We also tested a timeseries of 3-hourly MERRA-2 reanalysis Black Carbon (BC) concentration data for 5 years from 2012–2016 and explored pollution trends over time. We then used MODIS active fires, and synoptic wind patterns to attribute variability in Hanoi pollution to different sources. Because Hanoi is within the Red River Delta where rice residue burning is prominent, we explored trends to see if the residue burning signal is evident in the UVAI or BC data. Further, as the region experiences monsoon-influenced rainfall patterns, we adjusted the BC data based on daily rainfall amounts. Results indicated forest biomass burning from Northwest Vietnam and Laos impacts Hanoi air quality during the peak UVAI months of March and April. Whereas, during local rice residue burning months of June and October, no increase in UVAI is observed, with slight BC increase in October only. During the peak BC months of December and January, wind patterns indicated pollutant transport from southern China megacity areas. Results also indicated severe pollution episodes during December 2013 and January 2014. We observed significantly higher BC concentrations during nighttime than daytime with peaks generally between 2130 and 0030 local time. Our results highlight the need for better air pollution monitoring systems to capture episodic pollution events and their surface-level impacts, such as rice residue burning in cloud-prone regions in general and Hanoi, Vietnam in particular. PMID:29738543

Evaluating the air quality impacts of the 2008 Beijing Olympic Games: On-road emission factors and black carbon profiles

NASA Astrophysics Data System (ADS)

Wang, Xing; Westerdahl, Dane; Chen, Lung Chi; Wu, Ye; Hao, Jiming; Pan, Xiaochuan; Guo, Xinbiao; Zhang, K. Max

The aggressive traffic interventions and emission control measures implemented to improve air quality during the 2008 Beijing Olympic Games created a valuable case study to evaluate the effectiveness of these measures on mitigating air pollution and protecting public health. In this paper, we report the results from our field campaign in summer 2008 on the on-road emission factors of carbon monoxide, black carbon (BC) and ultrafine particles (UFP) as well as the ambient BC concentrations. The fleet average emission factors for light-duty gasoline vehicles (LDGV) showed considerable reduction in the Olympic year (2008) compared to the pre-Olympic year (2007). Our measurement of Black Carbon (BC), a primary pollutant, at different elevations at the ambient site suggests consistent decrease in BC concentrations as the height increased near the ground level, which indicates that the nearby ground level sources, probably dominated by traffic, contributed to a large portion of BC concentrations in the lower atmospheric layer in Beijing during summertime. These observations indicate that people living in near ground levels experience higher exposures than those living in higher floors in Beijing. The BC diurnal patterns on days when traffic control were in place during the Olympic Games were compared to those on non-traffic-control days in both 2007 and in 2008. These patterns strongly suggest that diesel trucks are a major source of summertime BC in Beijing. The median BC concentration on Olympic days was 3.7 μg m -3, which was dramatically lower than the value on non-traffic-control days, indicating the effectiveness of traffic control regulations in BC reduction in Beijing.

Enhancement of chromate reduction in soils by surface modified biochar.

PubMed

Mandal, Sanchita; Sarkar, Binoy; Bolan, Nanthi; Ok, Yong Sik; Naidu, Ravi

2017-01-15

Chromium (Cr) is one of the common metals present in the soils and may have an extremely deleterious environmental impact depending on its redox state. Among two common forms, trivalent Cr(III) is less toxic than hexavalent Cr(VI) in soils. Carbon (C) based materials including biochar could be used to alleviate Cr toxicity through converting Cr(VI) to Cr(III). Incubation experiments were conducted to examine Cr(VI) reduction in different soils (Soil 1: pH 7.5 and Soil 2: pH 5.5) with three manures from poultry (PM), cow (CM) and sheep (SM), three respective manure-derived biochars (PM biochar (PM-BC), CM biochar (CM-BC) and SM biochar (SM-BC)) and two modified biochars (modified PM-BC (PM-BC-M) and modified SM-BC (SM-BC-M)). Modified biochar was synthesized by incorporating chitosan and zerovalent iron (ZVI) during pyrolysis. Among biochars, highest Cr(VI) reduction was observed with PM-BC application (5%; w/w) (up to 88.12 mg kg -1 ; 45% reduction) in Soil 2 (pH 5.5). The modified biochars enhanced Cr(VI) reduction by 55% (SM-BC-M) compared to manure (29%, SM) and manure-derived biochars (40% reduction, SM-BC). Among the modified biochars, SM-BC-M showed a higher Cr(VI) reduction rate (55%) than PM-BC-M (48%) in Soil 2. Various oxygen-containing surface functional groups such as phenolic, carboxyl, carbonyl, etc. on biochar surface might act as a proton donor for Cr(VI) reduction and subsequent Cr(III) adsorption. This study underpins the immense potential of modified biochar in remediation of Cr(VI) contaminated soils. Copyright © 2016 Elsevier Ltd. All rights reserved.

Dirty Snow, Atmospheric Warming, and Climate Feedbacks from Boreal Black Carbon Emissions

NASA Astrophysics Data System (ADS)

Flanner, M. G.; Zender, C. S.; Randerson, J. T.; Jin, Y.

2005-12-01

Black carbon (BC) emitted from boreal fires darkens snow and sea-ice surfaces, increases solar absorption in the atmosphere, and decreases the incident flux at the surface. Although global surface forcing of darkened snow/ice is small relative to atmospheric forcing, the former directly triggers ice-albedo feedback, whereas the latter directly alters the atmospheric lapse rate. This highlights the importance of examining climate feedback strength as well as instantaneous forcings. We used a coupled land-atmosphere GCM (NCAR CAM3) to compare the relative forcings and climate feedbacks of BC emitted from a suite of boreal forest fires over the last decade, accounting for both enhanced snow/ice and atmospheric absorption by BC. The net change in absorbed energy at the surface was about three times greater than the instantaneous surface forcing when BC interactively heated the snow. Timing and location of fires determined the magnitude of darkened snow/ice feedback potential. We also assessed climate feedback strength from BC emitted globally during extreme high and low fire years, including the 1998 fire season.

Analyzing 20 years of Black Carbon measurements in Germany

NASA Astrophysics Data System (ADS)

Kutzner, R. D.; Quedenau, J.; Kuik, F.; von Schneidemesser, E.; Schmale, J.

2016-12-01

Black Carbon (BC) is an important short-lived climate-forcing pollutant contributing to global warming through absorption of sunlight. In addition, BC, as a component of particulate matter (PM) exerts adverse health effects. Anthropogenic emission sources of BC include residential heating, transport, and agricultural fires, and the dominant natural emission source is wildfires. Despite the adverse effects of BC, legislation that requires mandatory monitoring of BC concentrations does not currently exist in the European Union (EU). Instead, BC is only indirectly monitored as component of PM10 and PM2.5 (PM with a diameter smaller 10 µm and 2.5 µm, respectively). Before the introduction of mandatory PM10 and PM2.5 monitoring in the EU in 2005 and 2015, respectively, `black smoke' (BS), a surrogate for BC, was a required measurement in Germany from the early 1990s. The annual mean limit value was 14 µg/m3 from 1995 and 8 µg/m³ from 1998. In 2004, many measurements were stopped, with the repeal of the regulations. In most German federal states a limited number BC monitoring stations continued to operate. We present a synthesis of BC data from 213 stations across Germany covering the period between 1994 and 2014. Due to the lack of a standardized method and respective legislation, the data set is very heterogeneous relying on twelve different measurement methods including chemical, optical, and thermal-optical methods. Stations include, among others, urban background, traffic and rural. We highlight results from the year 2009, as it is the year with the largest measurement coverage based on the same measurement method, with 28 stations. Further, we calculated trends in BC concentrations for 13 stations with at least 10 years of data, for median concentrations, as well as 5th percentile (background) and 95th percentile (peak episodes). Preliminary results suggest that concentrations have generally declined, with a larger trend at traffic stations compared to urban background stations between 2005 and 2014. However, preliminary results also show that concentrations are highest during the colder months, likely linked to residential heating.

Impacts of absorbing aerosol deposition on snowpack and hydrologic cycle in the Rocky Mountain region based on variable-resolution CESM (VR-CESM) simulations

NASA Astrophysics Data System (ADS)

Wu, Chenglai; Liu, Xiaohong; Lin, Zhaohui; Rahimi-Esfarjani, Stefan R.; Lu, Zheng

2018-01-01

The deposition of light-absorbing aerosols (LAAs), such as black carbon (BC) and dust, onto snow cover has been suggested to reduce the snow albedo and modulate the snowpack and consequent hydrologic cycle. In this study we use the variable-resolution Community Earth System Model (VR-CESM) with a regionally refined high-resolution (0.125°) grid to quantify the impacts of LAAs in snow in the Rocky Mountain region during the period 1981-2005. We first evaluate the model simulation of LAA concentrations both near the surface and in snow and then investigate the snowpack and runoff changes induced by LAAs in snow. The model simulates similar magnitudes of near-surface atmospheric dust concentrations as observations in the Rocky Mountain region. Although the model underestimates near-surface atmospheric BC concentrations, the model overestimates BC-in-snow concentrations by 35 % on average. The regional mean surface radiative effect (SRE) due to LAAs in snow reaches up to 0.6-1.7 W m-2 in spring, and dust contributes to about 21-42 % of total SRE. Due to positive snow albedo feedbacks induced by the LAA SRE, snow water equivalent is reduced by 2-50 mm and snow cover fraction by 5-20 % in the two regions around the mountains (eastern Snake River Plain and southwestern Wyoming), corresponding to an increase in surface air temperature by 0.9-1.1 °C. During the snow melting period, LAAs accelerate the hydrologic cycle with monthly runoff increases of 0.15-1.00 mm day-1 in April-May and reductions of 0.04-0.18 mm day-1 in June-July in the mountainous regions. Of all the mountainous regions, the Southern Rockies experience the largest reduction of total runoff by 15 % during the later stage of snowmelt (i.e., June and July). Compared to previous studies based on field observations, our estimation of dust-induced SRE is generally 1 order of magnitude smaller in the Southern Rockies, which is ascribed to the omission of larger dust particles (with the diameter > 10 µm) in the model. This calls for the inclusion of larger dust particles in the model to reduce the discrepancies. Overall these results highlight the potentially important role of LAA interactions with snowpack and the subsequent impacts on the hydrologic cycles across the Rocky Mountains.

Factors Controlling Black Carbon Deposition in Snow in the Arctic

NASA Astrophysics Data System (ADS)

Qi, L.; Li, Q.; He, C.; Li, Y.

2015-12-01

This study evaluates the sensitivity of black carbon (BC) concentration in snow in the Arctic to BC emissions, dry deposition and wet scavenging efficiency using a 3D global chemical transport model GEOS-Chem driven by meteorological field GEOS-5. With all improvements, simulated median BC concentration in snow agrees with observation (19.2 ng g-1) within 10%, down from -40% in the default GEOS-Chem. When the previously missed gas flaring emissions (mainly located in Russia) are included, the total BC emission in the Arctic increases by 70%. The simulated BC in snow increases by 1-7 ng g-1, with the largest improvement in Russia. The discrepancy of median BC in snow in the whole Arctic reduces from -40% to -20%. In addition, recent measurements of BC dry deposition velocity suggest that the constant deposition velocity of 0.03 cm s-1 over snow and ice used in the GEOS-Chem is too low. So we apply resistance-in-series method to calculate the dry deposition velocity over snow and ice and the resulted dry deposition velocity ranges from 0.03 to 0.24 cm s-1. However, the simulated total BC deposition flux in the Arctic and BC in snow does not change, because the increased dry deposition flux has been compensated by decreased wet deposition flux. However, the fraction of dry deposition to total deposition increases from 16% to 25%. This may affect the mixing of BC and snow particles and further affect the radative forcing of BC deposited in snow. Finally, we reduced the scavenging efficiency of BC in mixed-phase clouds to account for the effect of Wegener-Bergeron-Findeisen (WBF) process based on recent observations. The simulated BC concentration in snow increases by 10-100%, with the largest increase in Greenland (100%), Tromsø (50%), Alaska (40%), and Canadian Arctic (30%). Annual BC loading in the Arctic increases from 0.25 to 0.43 mg m-2 and the lifetime of BC increases from 9.2 to 16.3 days. This indicates that BC simulation in the Arctic is really sensitive to the representation of BC scavenging efficiency. More measurements are needed to better understand the BC-cloud interaction and to constrain the model.

Roosevelt Island Climate Evolution Project (RICE): A 65 Kyr ice core record of black carbon aerosol deposition to the Ross Ice Shelf, West Antarctica.

NASA Astrophysics Data System (ADS)

Edwards, Ross; Bertler, Nancy; Tuohy, Andrea; Neff, Peter; Proemse, Bernedette; Feiteng, Wang; Goodwin, Ian; Hogan, Chad

2015-04-01

Emitted by fires, black carbon aerosols (rBC) perturb the atmosphere's physical and chemical properties and are climatically active. Sedimentary charcoal and other paleo-fire records suggest that rBC emissions have varied significantly in the past due to human activity and climate variability. However, few paleo rBC records exist to constrain reconstructions of the past rBC atmospheric distribution and its climate interaction. As part of the international Roosevelt Island Climate Evolution (RICE) project, we have developed an Antarctic rBC ice core record spanning the past ~65 Kyr. The RICE deep ice core was drilled from the Roosevelt Island ice dome in West Antarctica from 2011 to 2013. The high depth resolution (~ 1 cm) record was developed using a single particle intracavity laser-induced incandescence soot photometer (SP2) coupled to an ice core melter system. The rBC record displays sub-annual variability consistent with both austral dry-season and summer biomass burning. The record exhibits significant decadal to millennial-scale variability consistent with known changes in climate. Glacial rBC concentrations were much lower than Holocene concentrations with the exception of several periods of abrupt increases in rBC. The transition from glacial to interglacial rBC concentrations occurred over a much longer time relative to other ice core climate proxies such as water isotopes and suggests . The protracted increase in rBC during the transition may reflected Southern hemisphere ecosystem / fire regime changes in response to hydroclimate and human activity.

The atmospheric lifetime of black carbon

NASA Astrophysics Data System (ADS)

Cape, J. N.; Coyle, M.; Dumitrean, P.

2012-11-01

Black carbon (BC) in the atmosphere contributes to the human health effects of particulate matter and contributes to radiative forcing of climate. The lifetime of BC, particularly the smaller particle sizes (PM2.5) which can be transported over long distances, is therefore an important factor in determining the range of such effects, and the spatial footprint of emission controls. Theory and models suggest that the typical lifetime of BC is around one week. The frequency distributions of measurements of a range of hydrocarbons at a remote rural site in southern Scotland (Auchencorth Moss) between 2007 and 2010 have been used to quantify the relationship between atmospheric lifetime and the geometric standard deviation of observed concentration. The analysis relies on an assumed common major emission source for hydrocarbons and BC, namely diesel-engined vehicles. The logarithm of the standard deviation of the log-transformed concentration data is linearly related to hydrocarbon lifetime, and the same statistic for BC can be used to assess the lifetime of BC relative to the hydrocarbons. Annual average data show BC lifetimes in the range 4-12 days, for an assumed OH concentration of 7 × 105 cm-3. At this site there is little difference in BC lifetime between winter and summer, despite a 3-fold difference in relative hydrocarbon lifetimes. This observation confirms the role of wet deposition as an important removal process for BC, as there is no difference in precipitation between winter and summer at this site. BC lifetime was significantly greater in 2010, which had 23% less rainfall than the preceding 3 years.

PM2.5 and Black carbon enhancement at Socheongcho Ocean Research Station in the Yellow Sea

NASA Astrophysics Data System (ADS)

Jeon, H.; Rhee, H.; Lee, M.; JinYong, J.; Min, I.; Shim, J.

2017-12-01

Socheongcho Ocean Research Station (SORS) has been established in northern Yellow Sea by the Korea Institute of Ocean Science and Technology (KIOST). At SORS, PM2.5 and Black carbon (BC) were measured every 10 minutes during October 2014 June 2017 using beta-ray absorption method (FH62C14, Thermo. Inc, USA) and Multi Angle Absorption Photometer (MAAP; Model 5012, Thermo. Inc, USA), respectively. In addition, CO, CO2 and CH4 were determined by Cavity Ring Down Spectroscopy (CRDS; Model G2401, Picarro. Inc, USA). Measurements were intermittently interrupted for SORS maintenance reasons. For BC and PM2.5, the mean, 90th %tile and maximum concentrations were 1.16, 2.29, and 20.07 ug/m3 and 25, 48, and 177 ug/m3, respectively. There was no clear diurnal variation observed for both species. PM2.5 and BC concentrations were higher in cold seasons than in warm seasons. The highest PM2.5 and BC concentrations (>99th %tile) were more frequently observed in winter. Particularly, the extremely high BC were sporadically observed and lasted for no longer than 1 hour. The possible sources of PM2.5 and BC were examined using Conditional Probability Function (CPF), Potential Source Contribution (PSCF), and Concentration Weighted Trajectory (CWT) analysis. The results suggest the dominant influence from China, particularly for high concentrations.

The ``Micro'' Aethalometer - an enabling technology for new applications in the measurement of Aerosol Black Carbon

NASA Astrophysics Data System (ADS)

Hansen, A. D.; Močnik, G.

2010-12-01

Aerosol Black Carbon (BC) is a tracer for combustion emissions; a primary indicator of adverse health effects; and the second leading contributor to Global Climate Change. The “Micro” Aethalometer is a recently-developed miniature instrument that makes a real-time measurement of BC on a very short timebase in a self-contained, battery-powered package that is lightweight and pocket sized. This technological development critically enables new areas of research: Measurements of the vertical profile of BC, by carrying the sampler aloft on a balloon (tethered or released) or aircraft (piloted or UAV); Estimates of the concentration of BC in the troposphere and lower stratosphere in the 8 - 12 km. altitude range, by measurements in the passenger cabin during commercial air travel; Epidemiological studies of personal exposure to BC, by carrying the sampler on a subject person in health studies; Measurements of the concentration of BC in rural and remote regions, by means of a small, battery-powered instrument that is convenient to deploy; measurements of high concentrations of “smoke” in indoor and outdoor environments in developing countries; Unobtrusive monitoring of BC infiltration into indoor environments, by means of a small, quiet instrument that can be placed in publicly-used spaces, school classrooms, museums, and other potentially-impacted locations; Adaptation of the technology to the direct source measurement of BC concentrations in emissions from diesel exhausts, combustion plumes, and other sources. We will show examples of data from various recent projects to illustrate the capabilities and applications of this new instrument.

Near-road sampling of PM2. 5, BC, and fine-particle chemical components in Kathmandu Valley, Nepal

NASA Astrophysics Data System (ADS)

Shakya, Kabindra M.; Rupakheti, Maheswar; Shahi, Anima; Maskey, Rejina; Pradhan, Bidya; Panday, Arnico; Puppala, Siva P.; Lawrence, Mark; Peltier, Richard E.

2017-06-01

Semicontinuous PM2. 5 and black carbon (BC) concentrations, and 24 h integrated PM2. 5 filter samples were collected near roadways in the Kathmandu Valley, Nepal. Instruments were carried by a group of volunteer traffic police officers in the vicinity of six major roadway intersections in the Kathmandu Valley across two sampling periods in 2014. Daily PM2. 5 filter samples were analyzed for water-soluble inorganic ions, elemental carbon (EC) and organic carbon (OC), and 24 elements. Mean PM2. 5 and BC concentrations were 124.76 µg m-3 and 16.74 µgC m-3 during the drier spring sampling period, and 45.92 µg m-3 and 13.46 µgC m-3 during monsoonal sampling. Despite the lower monsoonal PM2. 5 concentrations, BC and several elements were not significantly lower during the monsoon, which indicates an important contribution of vehicle-related emissions throughout both seasons in this region. During the monsoon, there was an enhanced contribution of chemical species (elements and water-soluble inorganic ions), except secondary inorganic ions, and BC to PM2. 5 (crustal elements: 19 %; heavy metals: 5 %; and BC: 39 %) compared to those in spring (crustal elements: 9 %; heavy metals: 1 %; and BC: 18 %). Silica, calcium, aluminum, and iron were the most abundant elements during both spring and the monsoon, with total concentrations of 12.13 and 8.85 µg m-3, respectively. PM2. 5 and BC showed less spatial variation compared to that for individual chemical species.

Efficiency and mechanisms of Cd removal from aqueous solution by biochar derived from water hyacinth (Eichornia crassipes).

PubMed

Zhang, Feng; Wang, Xin; Yin, Daixia; Peng, Bo; Tan, Changyin; Liu, Yunguo; Tan, Xiaofei; Wu, Shixue

2015-04-15

This study investigated the efficiency and mechanisms of Cd removal by biochar pyrolyzed from water hyacinth (BC) at 250-550 °C. BC450 out-performed the other BCs at varying Cd concentrations and can remove nearly 100% Cd from aqueous solution within 1 h at initial Cd ≤ 50 mg l(-1). The process of Cd sorption by BC450 followed the pseudo-second order kinetics with the equilibrium being achieved after 24 h with initial Cd ranging from 100 to 500 mg l(-1). The maximum Cd sorption capacity of BC450 was estimated to be 70.3 mg g(-1) based on Langmuir model, which is prominent among a range of low-cost sorbents. Based on the balance analysis between cations released and Cd sorbed onto BC450 in combination with SEM-EDX and XPS data, ion-exchange followed by surface complexation is proposed as the dominant mechanism responsible for Cd immobilization by BC450. In parallel, XRD analysis also suggested the formation of insoluble Cd minerals (CdCO3, Cd3P2, Cd3(PO4)2 and K4CdCl6) from either (co)-precipitation or ion exchange. Results from this study highlighted that the conversion of water hyacinth into biochar is a promising method to achieve effective Cd immobilization and improved management of this highly problematic invasive species. Copyright © 2015 Elsevier Ltd. All rights reserved.

Black carbon surface oxidation and organic composition of beech-wood soot aerosols

NASA Astrophysics Data System (ADS)

Corbin, J. C.; Lohmann, U.; Sierau, B.; Keller, A.; Burtscher, H.; Mensah, A. A.

2015-10-01

Soot particles are the most strongly light-absorbing particles commonly found in the atmosphere. They are major contributors to the radiative budget of the Earth and to the toxicity of atmospheric pollution. Atmospheric aging of soot may change its health- and climate-relevant properties by oxidizing the primary black carbon (BC) or organic particulate matter (OM) which, together with ash, comprise soot. This atmospheric aging, which entails the condensation of secondary particulate matter as well as the oxidation of the primary OM and BC emissions, is currently poorly understood. In this study, atmospheric aging of wood-stove soot aerosols was simulated in a continuous-flow reactor. The composition of fresh and aged soot particles was measured in real time by a dual-vaporizer aerosol-particle mass spectrometer (SP-AMS). The dual-vaporizer SP-AMS provided information on the OM and BC components of the soot as well as on refractory components internally mixed with BC. By switching the SP-AMS laser vaporizer off and using only the AMS thermal vaporizer (at 600 °C), information on the OM component only was obtained. In both modes, OM appeared to be generated largely by cellulose and/or hemicellulose pyrolysis and was only present in large amounts when new wood was added to the stove. In SP-AMS mode, BC signals otherwise dominated the mass spectrum. These signals consisted of ions related to refractory BC (rBC, C1-5+), oxygenated carbonaceous ions (CO1-2+), potassium (K+), and water (H2O+ and related fragments). The C4+ : C3+ ratio, but not the C1+ : C3+ ratio, was consistent with the BC-structure trends of Corbin et al. (2015c). The CO1-2+ signals likely originated from BC surface groups: upon aging, both CO+ and CO2+ increased relative to C1-3+ while CO2+ simultaneously increased relative to CO+. Factor analysis (positive matrix factorization) of SP-AMS and AMS data, using a modified error model to address peak-integration uncertainties, indicated that the surface composition of the BC was approximately constant across all stages of combustion for both fresh and aged samples. These results represent the first time-resolved measurements of in situ BC surface aging and suggest that the surface of beech-wood BC may be modelled as a single chemical species.

Global Civil Aviation Black Carbon Particle Mass and Number Emissions

NASA Astrophysics Data System (ADS)

Stettler, M. E. J.

2015-12-01

Black carbon (BC) is a product of incomplete combustion emitted by aircraft engines. In the atmosphere, BC particles strongly absorb incoming solar radiation and influence cloud formation processes leading to highly uncertain, but likely net positive warming of the earth's atmosphere. At cruise altitude, BC particle number emissions can influence the concentration of ice nuclei that can lead to contrail formation, with significant and highly uncertainty climate impacts. BC particles emitted by aircraft engines also degrade air quality in the vicinity of airports and globally. A significant contribution to the uncertainty in environmental impacts of aviation BC emissions is the uncertainty in emissions inventories. Previous work has shown that global aviation BC mass emissions are likely to have been underestimated by a factor of three. In this study, we present an updated global BC particle number inventory and evaluate parameters that contribute to uncertainty using global sensitivity analysis techniques. The method of calculating particle number from mass utilises a description of the mobility of fractal aggregates and uses the geometric mean diameter, geometric standard deviation, mass-mobility exponent, primary particle diameter and material density to relate the particle number concentration to the total mass concentration. Model results show good agreement with existing measurements of aircraft BC emissions at ground level and at cruise altitude. It is hoped that the results of this study can be applied to estimate direct and indirect climate impacts of aviation BC emissions in future studies.

Sources and transport of black carbon at the California-Mexico border

NASA Astrophysics Data System (ADS)

Shores, Christopher A.; Klapmeyer, Michael E.; Quadros, Marina E.; Marr, Linsey C.

2013-05-01

At international border areas that suffer from poor air quality, assessment of pollutant sources and transport across the border is important for designing effective air quality management strategies. As part of the Cal-Mex 2010 field campaign at the US-Mexico border in San Diego and Tijuana, we measured black carbon (BC) concentrations at three locations in Mexico and one in the United States. The measurements were intended to support the following objectives: to characterize the spatial and temporal variability in BC, to estimate the BC emission inventory, to identify potential source areas of BC emissions, and to assess the cross-border transport of BC. Concentrations at Parque Morelos, the campaign's supersite, averaged 2.2 μg m-3 and reached a maximum value of 55.9 μg m-3 (1-min average). Sharp, regularly occurring peaks around midnight were suggestive of clandestine industrial activity. BC concentrations were more than two times higher, on average, in Tijuana compared to San Diego. BC and carbon monoxide (CO) were strongly correlated at the three sites in Mexico. The ΔBC/ΔCO ratio of 5.6 ± 0.5 μg m-3 ppm-1 in Tijuana, or 4.7 ± 0.5 μg m-3 ppm-1 when adjusted for seasonal temperature effects to represent an annual average, was comparable to that in other urban areas. Tijuana's emissions of BC were estimated to be 230-890 metric tons per year, 6-23% of those estimated for San Diego. Large uncertainties in this estimate stem mainly from uncertainties in the CO emission inventory, and the lower end of the estimate is more likely to be accurate. Patterns in concentrations and winds suggest that BC in Tijuana was usually of local origin. Under typical summertime conditions such as those observed during the study, transport from Tijuana into the US was common, crossing the border in a northeasterly direction, sometimes as far east as Imperial County at the eastern edge of California.

Dissolved black carbon in the global cryosphere: Concentrations and chemical signatures

NASA Astrophysics Data System (ADS)

Khan, Alia L.; Wagner, Sasha; Jaffe, Rudolf; Xian, Peng; Williams, Mark; Armstrong, Richard; McKnight, Diane

2017-06-01

Black carbon (BC) is derived from the incomplete combustion of biomass and fossil fuels and can enhance glacial recession when deposited on snow and ice surfaces. Here we explore the influence of environmental conditions and the proximity to anthropogenic sources on the concentration and composition of dissolved black carbon (DBC), as measured by benzenepolycaroxylic acid (BPCA) markers, across snow, lakes, and streams from the global cryosphere. Data are presented from Antarctica, the Arctic, and high alpine regions of the Himalayas, Rockies, Andes, and Alps. DBC concentrations spanned from 0.62 μg/L to 170 μg/L. The median and (2.5, 97.5) quantiles in the pristine samples were 1.8 μg/L (0.62, 12), and nonpristine samples were 21 μg/L (1.6, 170). DBC is susceptible to photodegradation when exposed to solar radiation. This process leads to a less condensed BPCA signature. In general, DBC across the data set was composed of less polycondensed DBC. However, DBC from the Greenland Ice Sheet (GRIS) had a highly condensed BPCA molecular signature. This could be due to recent deposition of BC from Canadian wildfires. Variation in DBC appears to be driven by a combination of photochemical processing and the source combustion conditions under which the DBC was formed. Overall, DBC was found to persist across the global cryosphere in both pristine and nonpristine snow and surface waters. The high concentration of DBC measured in supraglacial melt on the GRIS suggests that DBC can be mobilized across ice surfaces. This is significant because these processes may jointly exacerbate surface albedo reduction in the cryosphere.