scholarly journals Supplementary material to "Regional variability in black carbon and carbon monoxide ratio from long-term observations over East Asia: Assessment of representativeness for BC and CO emission inventories"

Author(s):  
Yongjoo Choi ◽  
Yugo Kanaya ◽  
Seung-Myung Park ◽  
Atsushi Matsuki ◽  
Yasuhiro Sadanaga ◽  
...  
2020 ◽  
Vol 20 (1) ◽  
pp. 83-98 ◽  
Author(s):  
Yongjoo Choi ◽  
Yugo Kanaya ◽  
Seung-Myung Park ◽  
Atsushi Matsuki ◽  
Yasuhiro Sadanaga ◽  
...  

Abstract. The black carbon (BC) and carbon monoxide (CO) emission ratios were estimated and compiled from long-term, harmonized observations of the ΔBC∕ΔCO ratios under conditions unaffected by wet deposition at four sites in East Asia, including two sites in South Korea (Baengnyeong and Gosan) and two sites in Japan (Noto and Fukuoka). Extended spatio-temporal coverage enabled estimation of the full seasonality and elucidation of the emission ratio in North Korea for the first time. The estimated ratios were used to validate the Regional Emission inventory in ASia (REAS) version 2.1 based on six study domains (“East China”, “North China”, “Northeast China”, South Korea, North Korea, and Japan). We found that the ΔBC∕ΔCO ratios from four sites converged into a narrow range (6.2–7.9 ng m−3 ppb−1), suggesting consistency in the results from independent observations and similarity in source profiles over the regions. The BC∕CO ratios from the REAS emission inventory (7.7 ng m−3 ppb−1 for East China – 23.2 ng m−3 ppb−1 for South Korea) were overestimated by factors of 1.1 for East China to 3.0 for South Korea, whereas the ratio for North Korea (3.7 ng m−3 ppb−1 from REAS) was underestimated by a factor of 2.0, most likely due to inaccurate emissions from the road transportation sector. Seasonal variation in the BC∕CO ratio from REAS was found to be the highest in winter (China and North Korea) or summer (South Korea and Japan), whereas the measured ΔBC∕ΔCO ratio was the highest in spring in all source regions, indicating the need for further characterization of the seasonality when creating a bottom-up emission inventory. At levels of administrative districts, overestimation in Seoul, the southwestern regions of South Korea, and Northeast China was noticeable, and underestimation was mainly observed in the western regions in North Korea, including Pyongyang. These diagnoses are useful for identifying regions where revisions in the inventory are necessary, providing guidance for the refinement of BC and CO emission rate estimates over East Asia.


2019 ◽  
Author(s):  
Yongjoo Choi ◽  
Yugo Kanaya ◽  
Seung-Myung Park ◽  
Atsushi Matsuki ◽  
Yasuhiro Sadanaga ◽  
...  

Abstract. The BC/CO emission ratios were estimated and compiled from long-term, harmonized observations of the ΔBC/ΔCO ratios under conditions unaffected by wet deposition at four sites in East Asia, including two sites in Korea (Baengnyeong and Gosan) and two sites in Japan (Noto and Fukuoka). Extended spatio-temporal coverage enabled estimation of full seasonality and elucidation of the emission ratio in North Korea, for the first time. The estimated ratios were used to validate the Regional Emission inventory in Asia (REAS) version 2.1 based on six study domains (East China, North China, Northeast China, South Korea, North Korea, and Japan). We found that the ΔBC/ΔCO ratios from four sites converged into a narrow range (6.2–7.9 ng m−3 ppb−1), suggesting consistency in the results from independent observations and similarity in source profiles over the regions. The BC/CO ratios from the REAS emission inventory (7.7 ng m−3 ppb−1 for East China – 23.2 ng m−3 ppb−1 for South Korea) were overestimated by factors of 1.1 for East China to 3.0 for South Korea, whereas the ratio for North Korea (3.7 ng m−3 ppb−1 from REAS) was underestimated by a factor of 2.0, most likely due to inaccurate emissions from the road transportation sector. Seasonal variation in the BC/CO ratio from REAS was found to be the highest in winter (China and North Korea) or summer (South Korea and Japan), whereas the measured ΔBC/ΔCO ratio was highest in spring in all source regions, indicating the need for further characterization of seasonality when creating a bottom-up emission inventory. At levels of administrative districts, overestimation in Seoul, the southwest regions of South Korea, and Northeast China was noticeable, and underestimation was mainly observed in the western regions in North Korea, including Pyongyang. These diagnoses are useful for identifying the regions where revisions in the inventory are necessary, providing guidance for refinement of BC and CO emission rate estimates over East Asia.


2013 ◽  
Vol 13 (15) ◽  
pp. 7567-7585 ◽  
Author(s):  
V. V. Petrenko ◽  
P. Martinerie ◽  
P. Novelli ◽  
D. M. Etheridge ◽  
I. Levin ◽  
...  

Abstract. We present the first reconstruction of the Northern Hemisphere (NH) high latitude atmospheric carbon monoxide (CO) mole fraction from Greenland firn air. Firn air samples were collected at three deep ice core sites in Greenland (NGRIP in 2001, Summit in 2006 and NEEM in 2008). CO records from the three sites agree well with each other as well as with recent atmospheric measurements, indicating that CO is well preserved in the firn at these sites. CO atmospheric history was reconstructed back to the year 1950 from the measurements using a combination of two forward models of gas transport in firn and an inverse model. The reconstructed history suggests that Arctic CO in 1950 was 140–150 nmol mol−1, which is higher than today's values. CO mole fractions rose by 10–15 nmol mol−1 from 1950 to the 1970s and peaked in the 1970s or early 1980s, followed by a ≈ 30 nmol mol−1 decline to today's levels. We compare the CO history with the atmospheric histories of methane, light hydrocarbons, molecular hydrogen, CO stable isotopes and hydroxyl radicals (OH), as well as with published CO emission inventories and results of a historical run from a chemistry-transport model. We find that the reconstructed Greenland CO history cannot be reconciled with available emission inventories unless unrealistically large changes in OH are assumed. We argue that the available CO emission inventories strongly underestimate historical NH emissions, and fail to capture the emission decline starting in the late 1970s, which was most likely due to reduced emissions from road transportation in North America and Europe.


2012 ◽  
Vol 12 (16) ◽  
pp. 7465-7474 ◽  
Author(s):  
E.-G. Brunke ◽  
R. Ebinghaus ◽  
H. H. Kock ◽  
C. Labuschagne ◽  
F. Slemr

Abstract. Mercury emissions in South Africa have so far been estimated only by a bottom-up approach from activities and emission factors for different processes. In this paper we derive GEM/CO (GEM being gaseous elemental mercury, Hg0), GEM/CO2, GEM/CH4, CO/CO2, CH4/CO2, and CH4/CO emission ratios from plumes observed during long-term monitoring of these species at Cape Point between March 2007 and December 2009. The average observed GEM/CO, GEM/CO2, GEM/CH4, CO/CO2, CH4/CO2, and CH4/CO emission ratios were 2.40 ± 2.65 pg m−3 ppb−1 (n = 47), 62.7 ± 80.2 pg m−3 ppm−1 (n = 44), 3.61 ± 4.66 pg m−3 ppb−1 (n = 46), 35.6 ± 25.4 ppb ppm−1 (n = 52), 20.2 ± 15.5 ppb ppm−1 (n = 48), and 0.876 ± 1.106 ppb ppb−1 (n = 42), respectively. The observed CO/CO2, CH4/CO2, and CH4/CO emission ratios agree within the combined uncertainties of the observations and emissions with the ratios calculated from EDGAR (version 4.2) CO2, CO, and CH4 inventories for South Africa and southern Africa (South Africa, Lesotho, Swaziland, Namibia, Botswana, Zimbabwe, and Mozambique) in 2007 and 2008 (inventories for 2009 are not available yet). Total elemental mercury emission of 13.1, 15.2, and 16.1 t Hg yr−1 are estimated independently using the GEM/CO, GEM/CO2, and GEM/CH4 emission ratios and the annual mean CO, CO2, and CH4 emissions, respectively, of South Africa in 2007 and 2008. The average of these independent estimates of 14.8 t GEM yr−1 is much less than the total emission of 257 t Hg yr−1 shown by older inventories which are now considered to be wrong. Considering the uncertainties of our emission estimate, of the emission inventories, and the fact that emission of GEM represents 50–78 % of all mercury emissions, our estimate is comparable to the currently cited GEM emissions in 2004 and somewhat smaller than emissions in 2006. A further increase of mercury emissions due to increasing electricity consumption will lead to a more pronounced difference. A quantitative assessment of the difference and its significance, however, will require emission inventories for the years of observations (2007–2009) as well as better data on the speciation of the total mercury emissions in South Africa.


2020 ◽  
Vol 12 (21) ◽  
pp. 3551
Author(s):  
Naghmeh Dehkhoda ◽  
Youngmin Noh ◽  
Sohee Joo

Absorption aerosol optical depth induced by black carbon (AAODBC) was retrieved using the depolarization ratio and single scattering albedo provided by the Aerosol Robotic Network (AERONET) inversion products over East Asia. Our analysis considered AERONET data from six sites in East Asia that are mostly affected by anthropogenic pollution, black carbon (BC) emissions, and natural mineral dust, during the period 2001–2018. We identified a rapid reduction in total aerosol optical depth (AODT) of −0.0106 yr−1 over Beijing, whereas no considerable trend was observed at the Korean and Japanese sites. The long-term data for AAODBC showed decreasing trends at all sites. We conclude that successful emission control policies were the major underlying driver of AODT and AAODBC reductions over East Asia, particularly in China, during the study period. Values of the AAODBC/AODT ratio revealed that, although these policies were successful, the Chinese government needs to undertake stricter measures toward reducing BC emissions. We found that AAODBC follows seasonal trends, peaking in the colder months. This suggests that in East Asia, particularly in China, domestic coal burning is still of concern.


2019 ◽  
Vol 210 ◽  
pp. 86-99 ◽  
Author(s):  
Shantanu Kumar Pani ◽  
Chang-Feng Ou-Yang ◽  
Sheng-Hsiang Wang ◽  
John A. Ogren ◽  
Patrick J. Sheridan ◽  
...  

2018 ◽  
Author(s):  
Debra Wunch ◽  
Geoffrey C. Toon ◽  
Nicholas M. Deutscher ◽  
Frank Hase ◽  
Justus Notholt ◽  
...  

Abstract. Using five long-running ground-based atmospheric observatories in Europe, we demonstrate the utility of long-term, stationary, ground-based measurements of atmospheric total columns for verifying annual methane emission inventories. Our results indicate that the methane emissions for the region in Europe between Orleans, Bremen, Bialystok, and Garmisch are overestimated by the state-of-the-art inventories Emission Database for Global Atmospheric Research (EDGAR) v4.2 FT2010 and TNO-MACC_III, possibly due to the disaggregation of emissions onto a grid. Uncertainties in the carbon monoxide inventories used to compute the methane emissions may contribute to the discrepancy between our inferred emissions and those from the inventories.


Sign in / Sign up

Export Citation Format

Share Document