scholarly journals Combining atmospheric and snow layer radiative transfer models to assess the solar radiative effects of black carbon in the Arctic

2020 ◽  
Author(s):  
Tobias Donth ◽  
Evelyn Jäkel ◽  
André Ehrlich ◽  
Bernd Heinold ◽  
Jacob Schacht ◽  
...  
Keyword(s):  
Radiative Transfer ◽  
Black Carbon ◽  
Heating Rate ◽  
Mass Concentration ◽  
Early Spring ◽  
Early Summer ◽  
The Arctic ◽  
Radiative Effect ◽  
Snow Layer ◽  
Surface Snow

Abstract. Solar radiative effects (cooling or warming) of black carbon (BC) particles suspended in the Arctic atmosphere and surface snow layer were explored by radiative transfer simulations on the basis of BC mass concentrations measured in pristine early summer and polluted early spring conditions under cloudless and cloudy conditions. To account for the radiative interactions between the black carbon containing snow surface layer and the atmosphere, a snow layer and an atmospheric radiative transfer model were coupled iteratively. For pristine summer conditions (no atmospheric BC) and a representative BC particle mass concentration of 5 ng g−1 in the surface snow layer, a positive solar radiative effect of +0.2 W m−2 was calculated for the surface radiative budget. Contrarily, a higher load of atmospheric BC representing springtime conditions, results in a slightly negative radiative effect of about −0.05 W m−2, even when the same BC mass concentration is suspended in the surface snow layer. This counteracting of atmospheric BC and BC suspended in the snow layer strongly depends on the snow optical properties determined by the snow specific surface area. However, it was found, that the atmospheric heating rate by water vapor or clouds is one to two orders of magnitude larger than that by atmospheric BC. Similarly, the total heating rate (6 K day−1) within a snow pack due to absorption by the ice water, was found to be more than one order of magnitude larger than the heating rate of suspended BC (0.2 K day−1). The role of clouds in the estimation of the combined direct radiative BC effect (BC in snow and in atmosphere) was analyzed for the pristine early summer and the polluted early spring BC conditions. Both, the cooling effect by atmospheric BC, as well as the warming effect by BC suspended in snow are reduced in the presence of clouds.

scholarly journals Combining atmospheric and snow radiative transfer models to assess the solar radiative effects of black carbon in the Arctic

2020 ◽  
Vol 20 (13) ◽  
pp. 8139-8156
Author(s):  
Tobias Donth ◽  
Evelyn Jäkel ◽  
André Ehrlich ◽  
Bernd Heinold ◽  
Jacob Schacht ◽  
...  
Keyword(s):  
Radiative Transfer ◽  
Arctic Ocean ◽  
Black Carbon ◽  
Heating Rate ◽  
Radiative Forcing ◽  
Mass Concentration ◽  
Early Summer ◽  
The Arctic ◽  
Snow Layer ◽  
Surface Snow

Abstract. The magnitude of solar radiative effects (cooling or warming) of black carbon (BC) particles embedded in the Arctic atmosphere and surface snow layer was explored on the basis of case studies. For this purpose, combined atmospheric and snow radiative transfer simulations were performed for cloudless and cloudy conditions on the basis of BC mass concentrations measured in pristine early summer and more polluted early spring conditions. The area of interest is the remote sea-ice-covered Arctic Ocean in the vicinity of Spitsbergen, northern Greenland, and northern Alaska typically not affected by local pollution. To account for the radiative interactions between the black-carbon-containing snow surface layer and the atmosphere, an atmospheric and snow radiative transfer model were coupled iteratively. For pristine summer conditions (no atmospheric BC, minimum solar zenith angles of 55∘) and a representative BC particle mass concentration of 5 ng g−1 in the surface snow layer, a positive daily mean solar radiative forcing of +0.2 W m−2 was calculated for the surface radiative budget. A higher load of atmospheric BC representing early springtime conditions results in a slightly negative mean radiative forcing at the surface of about −0.05 W m−2, even when the low BC mass concentration measured in the pristine early summer conditions was embedded in the surface snow layer. The total net surface radiative forcing combining the effects of BC embedded in the atmosphere and in the snow layer strongly depends on the snow optical properties (snow specific surface area and snow density). For the conditions over the Arctic Ocean analyzed in the simulations, it was found that the atmospheric heating rate by water vapor or clouds is 1 to 2 orders of magnitude larger than that by atmospheric BC. Similarly, the daily mean total heating rate (6 K d−1) within a snowpack due to absorption by the ice was more than 1 order of magnitude larger than that of atmospheric BC (0.2 K d−1). Also, it was shown that the cooling by atmospheric BC of the near-surface air and the warming effect by BC embedded in snow are reduced in the presence of clouds.

scholarly journals Variability in black carbon mass concentration in surface snow at Svalbard

2021 ◽  
Vol 21 (16) ◽  
pp. 12479-12493
Author(s):  
Michele Bertò ◽  
David Cappelletti ◽  
Elena Barbaro ◽  
Cristiano Varin ◽  
Jean-Charles Gallet ◽  
...  
Keyword(s):  
Black Carbon ◽  
Mass Concentration ◽  
Multiple Linear Regression Model ◽  
The Arctic ◽  
Snow Layer ◽  
Physico Chemical ◽  
Surface Snow ◽  
Carbon Mass ◽  
Precipitation Events ◽  
Observation Period

Abstract. Black carbon (BC) is a significant forcing agent in the Arctic, but substantial uncertainty remains to quantify its climate effects due to the complexity of the different mechanisms involved, in particular related to processes in the snowpack after deposition. In this study, we provide detailed and unique information on the evolution and variability in BC content in the upper surface snow layer during the spring period in Svalbard (Ny-Ålesund). A total of two different snow-sampling strategies were adopted during spring 2014 (from 1 April to 24 June) and during a specific period in 2015 (28 April to 1 May), providing the refractory BC (rBC) mass concentration variability on a seasonal variability with a daily resolution (hereafter seasonal/daily) and daily variability with an hourly sampling resolution (hereafter daily/hourly) timescales. The present work aims to identify which atmospheric variables could interact with and modify the mass concentration of BC in the upper snowpack, which is the snow layer where BC particles affects the snow albedo. Atmospheric, meteorological and snow-related physico-chemical parameters were considered in a multiple linear regression model to identify the factors that could explain the variations in BC mass concentrations during the observation period. Precipitation events were the main drivers of the BC variability during the seasonal experiment; however, in the high-resolution sampling, a negative association has been found. Snow metamorphism and the activation of local sources (Ny-Ålesund was a coal mine settlement) during the snowmelt periods appeared to play a non-negligible role. The statistical analysis suggests that the BC content in the snow is not directly associated to the atmospheric BC load.

scholarly journals Variability of Black Carbon mass concentration in surface snow at Svalbard

2021 ◽  
Author(s):  
Michele Bertò ◽  
David Cappelletti ◽  
Elena Barbaro ◽  
Cristiano Varin ◽  
Jean-Charles Gallet ◽  
...  
Keyword(s):  
Black Carbon ◽  
Mass Concentration ◽  
The Arctic ◽  
Sampling Strategies ◽  
Snow Layer ◽  
Physico Chemical ◽  
Surface Snow ◽  
Carbon Mass ◽  
Precipitation Events ◽  
Substantial Uncertainty

Abstract. Black Carbon (BC) is a significant forcing agent in the Arctic, but substantial uncertainty remains to quantify its climate effects due to the complexity of the different mechanisms involved, in particular related to processes in the snow-pack after deposition. In this study, we provide detailed and unique information on the evolution and variability of BC content in the upper surface snow layer during the spring period in Svalbard (Ny-Ålesund). Two different snow-sampling strategies were adopted during spring 2014 and 2015, providing the refractory BC (rBC) mass concentration variability on a seasonal/daily and daily/hourly time scales. The present work aims to identify which atmospheric variables could interact and modify the mass concentration of BC in the upper snowpack, the snow layer which BC particles affects the snow albedo. Despite the low BC mass concentrations, a relatively high daily variability was observed. Atmospheric, meteorological, and snow-related physico-chemical parameters were considered in a multiple statistical model to separate the factors determining observations. Precipitation events were the main drivers of the BC variability. Snow metamorphism and activation of local sources during the snow melting periods appeared to play a non-negligible role (wind resuspension in specific Arctic areas where coal mines were present). The BC content in the snow resulted in being statistically decoupled from the atmospheric BC load.

Radiative forcing over the Arctic of aerosols from the August 2017 Canadian and Greenlandic wildfires

2021 ◽  
Author(s):  
Filippo Calì Quaglia ◽  
Daniela Meloni ◽  
Alcide Giorgio di Sarra ◽  
Tatiana Di Iorio ◽  
Virginia Ciardini ◽  
...  
Keyword(s):  
Radiative Transfer ◽  
Radiative Forcing ◽  
Solar Zenith Angle ◽  
Surface Albedo ◽  
High Arctic ◽  
The Arctic ◽  
Radiative Transfer Model ◽  
Transfer Model ◽  
Aerosol Layer ◽  
Radiative Effect

<p>Extended and intense wildfires occurred in Northern Canada and, unexpectedly, on the Greenlandic West coast during summer 2017. The thick smoke plume emitted into the atmosphere was transported to the high Arctic, producing one of the largest impacts ever observed in the region. Evidence of Canadian and Greenlandic wildfires was recorded at the Thule High Arctic Atmospheric Observatory (THAAO, 76.5°N, 68.8°W, www.thuleatmos-it.it) by a suite of instruments managed by ENEA, INGV, Univ. of Florence, and NCAR. Ground-based observations of the radiation budget have allowed quantification of the surface radiative forcing at THAAO. </p><p>Excess biomass burning chemical tracers such as CO, HCN, H2CO, C2H6, and NH3 were  measured in the air column above Thule starting from August 19 until August 23. The aerosol optical depth (AOD) reached a peak value of about 0.9 on August 21, while an enhancement of wildfire compounds was  detected in PM10. The measured shortwave radiative forcing was -36.7 W/m2 at 78° solar zenith angle (SZA) for AOD=0.626.</p><p>MODTRAN6.0 radiative transfer model (Berk et al., 2014) was used to estimate the aerosol radiative effect and the heating rate profiles at 78° SZA. Measured temperature profiles, integrated water vapour, surface albedo, spectral AOD and aerosol extinction profiles from CALIOP onboard CALIPSO were used as model input. The peak  aerosol heating rate (+0.5 K/day) was  reached within the aerosol layer between 8 and 12 km, while the maximum radiative effect (-45.4 W/m2) is found at 3 km, below the largest aerosol layer.</p><p>The regional impact of the event that occurred on August 21 was investigated using a combination of atmospheric radiative transfer modelling with measurements of AOD and ground surface albedo from MODIS. The aerosol properties used in the radiative transfer model were constrained by in situ measurements from THAAO. Albedo data over the ocean have been obtained from Jin et al. (2004). Backward trajectories produced through HYSPLIT simulations (Stein et al., 2015) were also employed to trace biomass burning plumes.</p><p>The radiative forcing efficiency (RFE) over land and ocean was derived, finding values spanning from -3 W/m2 to -132 W/m2, depending on surface albedo and solar zenith angle. The fire plume covered a vast portion of the Arctic, with large values of the daily shortwave RF (< -50 W/m2) lasting for a few days. This large amount of aerosol is expected to influence cloud properties in the Arctic, producing significant indirect radiative effects.</p>

scholarly journals Black Carbon Seasonal and Diurnal Variation in surface snow in Svalbard and its Connections to Atmospheric Variables

2020 ◽  
Author(s):  
Michele Bertò ◽  
David Cappelletti ◽  
Elena Barbaro ◽  
Cristiano Varin ◽  
Jean-Charles Gallet ◽  
...  
Keyword(s):  
Black Carbon ◽  
The Arctic ◽  
Physico Chemical ◽  
Surface Snow ◽  
Seasonal And Diurnal Variation ◽  
Snow Precipitation ◽  
Common Association ◽  
Precipitation Events ◽  
Daily Time ◽  
Mass Concentrations

Abstract. Black Carbon (BC) is a major forcing agent in the Arctic but substantial uncertainty remains to quantify its climate effects due to the complexity of mechanisms involved. In this study, we provide unique information on processes driving the variability of BC mass concentration in surface snow in the Arctic. Two different snow-sampling strategies were adopted during spring 2014 and 2015, focusing on the refractory BC (rBC) mass Ny-Ålesund concentration daily/hourly variability on a seasonal/daily time scale (referred to as 80-days and 3-days experiments). Despite the low rBC mass concentrations (never exceeding 22 ng g−1), a daily variability of up to 4.5 ng g−1 was observed. Atmospheric, meteorological and snow-related physico-chemical parameters were considered in multiple statistical models to understand the factors behind the observed variation of rBC mass concentrations. Results indicate that the main drivers of the variation of rBC are the precipitations events, snow metamorphism (melting-refreezing cycles, surface hoar formation and sublimation) and the activation of local sources (wind resuspension) during the snow melting periods. The rBC in the snow seems de-coupled with the atmospheric BC load. Our results highlighted a common association of snow rBC with coarse mode particles number concentration and with snow precipitation events.

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

2014 ◽  
Vol 14 (5) ◽  
pp. 2399-2417 ◽  
Author(s):  
C. Jiao ◽  
M. G. Flanner ◽  
Y. Balkanski ◽  
S. E. Bauer ◽  
N. Bellouin ◽  
...  
Keyword(s):  
Sea Ice ◽  
Phase I ◽  
Black Carbon ◽  
Phase Ii ◽  
Full Range ◽  
Deposition Efficiency ◽  
The Arctic ◽  
Radiative Effect ◽  
Field Campaign ◽  
Scavenging Efficiency

Abstract. 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. Here, 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 which 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.

scholarly journals Impact of black carbon aerosol over Italian basin valleys: high-resolution measurements along vertical profiles, radiative forcing and heating rate

2014 ◽  
Vol 14 (18) ◽  
pp. 9641-9664 ◽  
Author(s):  
L. Ferrero ◽  
M. Castelli ◽  
B. S. Ferrini ◽  
M. Moscatelli ◽  
M. G. Perrone ◽  
...  
Keyword(s):  
High Resolution ◽  
Black Carbon ◽  
Heating Rate ◽  
Radiative Forcing ◽  
Transfer Model ◽  
Vertical Profiles ◽  
Radiative Effect ◽  
Mixing Height ◽  
Atmospheric Absorption ◽  
Height Range

Abstract. A systematic study of black carbon (BC) vertical profiles measured at high-resolution over three Italian basin valleys (Terni Valley, Po Valley and Passiria Valley) is presented. BC vertical profiles are scarcely available in literature. The campaign lasted 45 days and resulted in 120 measured vertical profiles. Besides the BC mass concentration, measurements along the vertical profiles also included aerosol size distributions in the optical particle counter range, chemical analysis of filter samples and a full set of meteorological parameters. Using the collected experimental data, we performed calculations of aerosol optical properties along the vertical profiles. The results, validated with AERONET data, were used as inputs to a radiative transfer model (libRadtran). The latter allowed an estimation of vertical profiles of the aerosol direct radiative effect, the atmospheric absorption and the heating rate in the lower troposphere. The present measurements revealed some common behaviors over the studied basin valleys. Specifically, at the mixing height, marked concentration drops of both BC (range: from −48.4 ± 5.3 to −69.1 ± 5.5%) and aerosols (range: from −23.9 ± 4.3 to −46.5 ± 7.3%) were found. The measured percentage decrease of BC was higher than that of aerosols: therefore, the BC aerosol fraction decreased upwards. Correspondingly, both the absorption and scattering coefficients decreased strongly across the mixing layer (range: from −47.6 ± 2.5 to −71.3 ± 3.0% and from −23.5 ± 0.8 to −61.2 ± 3.1%, respectively) resulting in a single-scattering albedo increase along height (range: from +4.9 ± 2.2 to +7.4 ± 1.0%). This behavior influenced the vertical distribution of the aerosol direct radiative effect and of the heating rate. In this respect, the highest atmospheric absorption of radiation was predicted below the mixing height (~ 2–3 times larger than above it) resulting in a heating rate characterized by a vertical negative gradient (range: from −2.6 ± 0.2 to −8.3 ± 1.2 K day−1 km−1). In conclusion, the present results suggest that the BC below the mixing height has the potential to promote a negative feedback on the atmospheric stability over basin valleys, weakening the ground-based thermal inversions and increasing the dispersal conditions.

scholarly journals Radiative effects of long-range-transported Saharan air layers as determined from airborne lidar measurements

2020 ◽  
Vol 20 (20) ◽  
pp. 12313-12327
Author(s):  
Manuel Gutleben ◽  
Silke Groß ◽  
Martin Wirth ◽  
Bernhard Mayer
Keyword(s):  
Water Vapor ◽  
Radiative Transfer ◽  
Heating Rate ◽  
Mineral Dust ◽  
Short Wave ◽  
Radiative Effect ◽  
Mixing Ratios ◽  
Long Wave ◽  
Lidar Measurements ◽  
Air Layers

Abstract. The radiative effect of long-range-transported Saharan air layers is investigated on the basis of simultaneous airborne high-spectral-resolution and differential-absorption lidar measurements in the vicinity of Barbados. Within the observed Saharan air layers, increased water vapor concentrations compared to the dry trade wind atmosphere are found. The measured profiles of aerosol optical properties and water vapor mixing ratios are used to characterize the atmospheric composition in radiative transfer calculations, to calculate radiative effects of moist Saharan air layers and to determine radiative heating rate profiles. An analysis based on three case studies reveals that the observed enhanced amounts of water vapor within Saharan air layers have a much stronger impact on heating rate calculations than mineral dust aerosol. Maximum mineral dust short-wave heating and long-wave cooling rates are found at altitudes of highest dust concentration (short wave: +0.5 K d−1; long wave: −0.2 K d−1; net: +0.3 K d−1). However, when considering both aerosol concentrations and measured water vapor mixing ratios in radiative transfer calculations, the maximum heating/cooling rates shift to the top of the dust layer (short wave: +2.2 K d−1; long wave: −6.0 to −7.0 K d−1; net: −4.0 to −5.0 K d−1). Additionally, the net heating rates decrease with height – indicating a destabilizing effect in the dust layers. Long-wave counter-radiation of Saharan air layers is found to reduce cooling at the tops of the subjacent marine boundary layers and might lead to less convective mixing in these layers. The overall short-wave radiative effect of mineral dust particles in Saharan air layers indicates a maximum magnitude of −40 W m−2 at surface level and a maximum of −25 W m−2 at the top of the atmosphere.

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