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In the context of China's "dual carbon" goal, emissions of air pollutants are expected to significantly decrease in the future. Thus, the direct climate effects of black carbon (BC) aerosols in East Asia are investigated under this goal using an updated regional climate and chemistry model. The simulated annual average BC concentration over East Asia is approximately 1.29 μg/m3 in the last decade. Compared to those in 2010–2020, both the BC column burden and instantaneous direct radiative forcing in East Asia decrease by more than 55% and 80%, respectively, in the carbon peak year (2030s) and the carbon neutrality year (2060s). Conversely, the BC effective radiative forcing (ERF) and regional climate responses to BC exhibit substantial nonlinearity to emission reduction, possibly resulting from different adjustments of thermal‐dynamic fields and clouds from BC‐radiation interactions. The regional mean BC ERF at the tropopause over East Asia is approximately +1.11 W/m2 in 2010–2020 while negative in the 2060s. BC‐radiation interactions in the present‐day impose a significant annual mean cooling of −0.2 to −0.5 K in central China but warming +0.3 K in the Tibetan Plateau. As China's BC emissions decline, surface temperature responses show a mixed picture compared to 2010–2020, with more cooling in eastern China and Tibet of −0.2 to −0.3 K in the 2030s, but more warming in central China of approximately +0.3 K by the 2060s. The Indian BC might play a more important role in East Asian climate with reduction of BC emissions in China. Plain Language Summary: Black carbon (BC) aerosols, which are among the air pollutants that will be reduced in China under the "dual carbon" goal, can have an impact on the regional climate by absorbing solar radiation. We use a regional climate model to simulate the climate effect of BC over East Asia under the "dual carbon" goal of China. The results showed that the BC concentration and column burden in East Asia, as well as the instantaneous direct radiative forcing, will decrease significantly under future regional emission reduction policies. However, the effective radiative forcing of BC and regional climate responses do not exhibit simple linear relationships with emissions. The BC‐induced atmospheric thermal‐dynamic anomalies are the main drivers of this nonlinearity. Similarly, BC emissions from India might also influence the East Asian climate. Key Points: The East Asian black carbon (BC) loadings and instantaneous direct radiative forcings significantly decrease under the "dual carbon" goal of ChinaThe BC induced regional climate changes show nonlinear responses to the BC emission reductionThe Indian BC might play an increasingly important role in East Asian climate with decreasing BC emissions in China [ABSTRACT FROM AUTHOR]

For the first‐time, analysis of a decade long measurement of Black Carbon mass concentration (BC) was carried out at a representative central Indo‐Gangetic Plain (IGP) location, Varanasi (25.30°N, 83.03°E, 79 m asl), from 2009 to 2021 to understand its physical, optical, and radiative impacts. During the 13‐year study period, the daily BC mass concentration was found to vary between 0.07 and 46.23 μg m−3 (mean 9.18 ± 6.53 μg m−3) and showed a strong inter‐annual and intra‐annual variations. The inter‐annual variability of BC showed a significant decreasing trend (−0.47 μg m−3 yr−1), with a maximum during the post‐monsoon (−1.86 μg m−3 yr−1) and minimum during the pre‐monsoon season (−0.31 μg m−3 yr−1). The Black Carbon Aerosol Radiative Forcing (BC‐ARF) at the top of the atmosphere (BC‐ARFT), surface (BC‐ARFS), and within the atmosphere (BC‐ARFA) was found to be 10.3 ± 6.4, −30.1 ± 18.9, and 40.5 ± 25.2 W m−2, respectively. BC‐ARF also showed a strong inter‐annual variability with a decreasing trend for BC‐ARFT (−0.47 W m−2 yr−1) and BC‐ARFA (−1.94 W m−2 yr−1), while it showed an increasing trend for BC‐ARFS (1.33 W m−2 yr−1). Concentrated weighted trajectories (CWT) and potential source contribution function (PSCF) analyses were performed at the station to determine the potential source sectors and transport routes of BC aerosols. These analyses revealed that the long‐range source of BC at Varanasi originates from the upper and lower IGP, central highlands, southern peninsular region, Pakistan, and even from the Central East Asia region. Plain Language Summary: Long‐term measurement of Black Carbon aerosol was done at a representative Central Indo‐Gangetic Plain (IGP) location, Varanasi, India, from 2009 to 2021. Analysis suggests significant interannual and intra‐annual variation of BC mass for the location. The important finding shows a significant decreasing trend in BC mass: the maximum for the post‐monsoon season and the minimum for the pre‐monsoon. Black Carbon‐Aerosol Radiative Forcing at the top of the atmosphere, at the surface, and within the atmosphere was found to be 10.3 ± 6.4, −30.1 ± 18.9, 40.5 ± 25.2 W m−2, respectively. Black Carbon Aerosol Radiative Forcing also showed a decreasing trend and implies an induced deceasing trend in the atmospheric heating rate. According to the concentrated weighted trajectory and potential source contribution function analyses, the upper and lower IGP, central highlands, southern peninsular region, Pakistan, and even the Central East Asia region are potential long‐range sources of BC at the Varanasi. Key Points: Black Carbon is decreasing over the central Indo‐Gangetic Plain (IGP) since 2009: maximum for post‐monsoon and minimum for pre‐monsoon seasonThe Black Carbon‐Aerosol Radiative Forcing (BC‐ARF) shows a decreasing trend over the central IGP on yearly scale since 2009Decreasing trend in BC‐ARF within the atmosphere relates to a decrease in BC mass concentration and suggests reduced atmospheric warming [ABSTRACT FROM AUTHOR]

Methods based on the absorption Ångström exponent (AAE) are widely used to estimate the absorption by brown carbon (BrC), and the estimated absorption by BrC can be significantly different from 0, even for pure black carbon (BC). However, few studies have systematically quantified the effects of BC microphysical properties. Moreover, the conditions under which AAE-based methods are applicable are still unclear. In this work, we used BC models partially coated with non-absorbing materials to calculate the total absorption. Since the total absorption is entirely due to BC, the estimated BrC absorption should be 0 if the retrieval methods are accurate. Thus, the ratio of the estimated BrC absorption to BC absorption (ABS BrC) should be the proportion of the BC absorption that is incorrectly attributed to BrC. The results show that a BC AAE of 1 can generally provide reasonable estimates for freshly emitted BC, since ABS BrC is generally in the range of -4.8 % to 2.7 % during that period. However, when BC aerosols are aged, ABS BrC can sometimes reach about 38.7 %. The wavelength dependence of the AAE (WDA) method does not necessarily improve the estimates; sometimes a negative ABSBrC of about -40.8 % is found for partially coated BC. By combining simulations of a global chemical transport model, this work also quantified the effects of BC microphysical properties on BrC global aerosol absorption optical depth (AAOD) estimates. The AAE = 1 method sometimes leads to a misassigned global mean AAOD of about - 0.43– 0.46×10-3 if the BC aerosols have a complex morphology. The WDA method does not necessarily improve the estimates. In our cases, the WDA methods based on spherical models could lead to a global-mean misassigned AAOD range of about -0.87 – 0.04×10-3. At the regional scale, the AAE = 1 method sometimes leads to a distributed AAOD of about -7.3 to 5.7×10-3 in some specific regions. Mie-theory-based WDA methods lead to an estimated AAOD error of about -22×10-3 in some regions (e.g., East Asia). This work also showed that the misattributed BrC absorption would lead to substantial uncertainties in the estimation of the global direct radiative forcing (DRF) of absorbing aerosols from different sources. [ABSTRACT FROM AUTHOR]

We apply a local ensemble transform Kalman smoother (LETKS) in combination with the global aerosol–climate model ECHAM–HAM to estimate aerosol emissions from POLDER-3/PARASOL (POLarization and Directionality of the Earth's Reflectances) observations for the year 2006. We assimilate aerosol optical depth at 550 mnm (AOD550), the Ångström exponent at 550 and 865 nm (AE550–865), and single-scattering albedo at 550 nm (SSA550) in order to improve modeled aerosol mass, size and absorption simultaneously. The new global aerosol emissions increase to 1419 Tgyr-1 (+ 28 %) for dust, 1850 Tgyr-1 (+ 75 %) for sea salt, 215 Tgyr-1 (+ 143 %) for organic aerosol and 13.3 Tgyr-1 (+ 75 %) for black carbon, while the sulfur dioxide emissions increase to 198 Tgyr-1 (+ 42 %) and the total deposition of sulfates to 293 Tgyr-1 (+ 39 %). Organic and black carbon emissions are much higher than their prior values from bottom-up inventories, with a stronger increase in biomass burning sources (+ 193 % and + 90 %) than in anthropogenic sources (115 % and 70 %). The evaluation of the experiments with POLDER (assimilated) and AERONET as well as MODIS Dark Target (independent) observations shows a clear improvement compared with the ECHAM–HAM control run. Specifically based on AERONET, the global mean error in AOD550 improves from - 0.094 to - 0.006, while absorption aerosol optical depth at 550 nm (AAOD550) improves from - 0.009 to - 0.004 after the assimilation. A smaller improvement is also observed in the AE550–865 mean absolute error (from 0.428 to 0.393), with a considerably higher improvement over isolated island sites at the ocean. The new dust emissions are closer to the ensemble median of AEROCOM I, AEROCOM III and CMIP5 as well as some of the previous assimilation studies. The new sea salt emissions have become closer to the reported emissions from previous studies. Indications of a missing fraction of coarse dust and sea salt particles are discussed. The biomass burning changes (based on POLDER) can be used as alternative biomass burning scaling factors for the Global Fire Assimilation System (GFAS) inventory distinctively estimated for organic carbon (2.93) and black carbon (1.90) instead of the recommended scaling of 3.4 (Kaiser et al., 2012). The estimated emissions are highly sensitive to the relative humidity due to aerosol water uptake, especially in the case of sulfates. We found that ECHAM–HAM, like most of the global climate models (GCMs) that participated in AEROCOM and CMIP6, overestimated the relative humidity compared with ERA5 and as a result the water uptake by aerosols, assuming the kappa values are not underestimated. If we use the ERA5 relative humidity, sulfate emissions must be further increased, as modeled sulfate AOD is lowered. Specifically, over East Asia, the lower AOD can be attributed to the underestimated precipitation and the lack of simulated nitrates in the model. [ABSTRACT FROM AUTHOR]

Aerosol mixtures, which are still unclear in current knowledge, may cause large uncertainties in aerosol climate effect assessments. To better understand this research gap, a well-developed online coupled regional climate-chemistry model is employed here to investigate the influences of different aerosol mixing states on the direct interactions between aerosols and the East Asian summer monsoon (EASM). The results show that anthropogenic aerosols have high-level loadings with heterogeneous spatial distributions in East Asia. Black carbon aerosol loading accounts for more than 13% of the totals in this region in summer. Thus, different aerosol mixing states cause very different aerosol single scattering albedos, with a variation of 0.27 in East Asia in summer. Consequently, the sign of the aerosol instantaneous direct radiative forcing at the top of the atmosphere is changed, varying from − 0.95 to + 1.50 W/m2 with increasing internal mixing aerosols. The influence of aerosol mixtures on regional climate responses seems to be weaker. The EASM circulation can be enhanced due to the warming effect of anthropogenic aerosols in the lower atmosphere, which further induces considerable aerosol accumulation associated with dynamic field anomaly, decrease in rainfall and so on, despite aerosol mixtures. However, this interaction between aerosols and the EASM will become more obvious if the aerosols are more mixed internally. Additionally, the differences in aerosol-induced EASM anomalies during the strongest and weakest monsoon index years are highly determined by the aerosol mixing states. The results here may further help us better address the environmental and climate change issues in East Asia. [ABSTRACT FROM AUTHOR]

The parameterization of deep convection is one of the primary sources of uncertainties in regional climate simulations. Due to computational constraints, long-term kilometer-scale simulations with explicit deep convection have been limited, especially over East Asia. We here conduct a pair of 10-years (2001–2010) reference simulations, one convection-parameterizing simulation at 12 km (0.11 ∘ ) resolution covering the CORDEX East Asia domain, and one 4.4-km (0.04 ∘ ) convection-permitting simulation over a subdomain. The two simulations are driven by the ERA5 reanalysis and the coarser-resolution simulation, respectively. The 4.4-km convection-permitting simulation noticeably improves the representation of the top-of-atmosphere outgoing longwave and shortwave radiation as well as precipitation intensity. In addition, sensitivity simulations are performed with perturbed sulfate and black carbon aerosols, considering the direct and semi-direct aerosol radiative effects. For the simulations with sulfate aerosol perturbations, the cloud radiative effect partly offsets the aerosol radiative effects. Decreasing sulfate aerosols leads to low-level warming, destabilizing the atmospheric stratification and thereby increasing mean precipitation and the frequency of wet days. Increasing sulfate aerosols leads to an approximately opposite response. For the simulations with black carbon aerosol perturbations, there is some near-surface warming for both increases and decreases in aerosol concentration. Also, there are significant changes in cloud cover, but changes in precipitation are comparatively weak. While for sulfate aerosol perturbations the response is approximately linear (in the sense that positive and negative perturbations yield approximately opposite effects), the response to black carbon aerosol perturbations is more complex and shows some nonlinearity, regardless of the treatment of deep convection in the simulations. We present a simple interpretation for this surprising result. [ABSTRACT FROM AUTHOR]

The absorption Ångström exponent (AAE)-based methods are widely used to estimate brown carbon (BrC) absorption, and the estimated BrC absorption can be significantly different from 0 even for pure black carbon (BC). However, few studies have systematically quantified the effects of BC microphysical properties. Moreover, it is still unclear under which conditions the AAE-based method is applicable. In this work, we used BC models partially coated with non-absorbing materials to calculate the total absorption. Since the total absorption is entirely from BC, the estimated BrC absorption should be 0 if the retrieval methods are accurate. Thus, the estimated BrC absorption (ABSBrC) should be the absorption from BC that is incorrectly attributed to BrC. The results show that a BC AAE of 1 can generally provide reasonable estimates for freshly emitted BC, since at this time ABSBrC is generally in the range of -3 % to 4.5 %. However, when BC aerosols are aged, ABSBrC of about 35 % could be observed. The WDA method does not necessarily improve the estimates, sometimes a negative ABSBrC of -40 % can be found for partially coated BC. By combining simulations of a global chemical transport model, this work also quantified the effects of BC microphysical properties on BrC global optical absorption aerosol depth (AAOD) estimates. The AAE = 1 method could sometimes lead to a misassigned global mean AAOD of about -0.4 – 0.5 × 10-3 if BC aerosols have a complex morphology, leading to a global mean direct radiation factor (DRF) of about -0.068 ± 0.0172 to +0.085 ± 0.0215 W/m2 from BC, which is incorrectly assigned to BrC. The WDA method does not necessarily improve the estimates. In our cases, the WDA methods based on the spherical models can lead to a range of about -0.9 – 0.05 × 10-3 of misassigned AAOD, which could lead to a global mean DRF error range of -0.153 ± 0.0387 to +0.0085 ± 0.0022 W/m2. At the regional scale, the AAE = 1 method in East Asia sometimes leads to a distributed AAOD of over 3 × 10-3, resulting in a BC DRF of about +0.51 ± 0.129 W/m2, which is incorrectly attributed to BrC. Mie theory-based WDA methods would lead to an estimated AAOD error of more than 6 × 10-3 in some regions (e.g., East Asia), resulting in an estimated misattributed DRF of +1.0 ± 0.258 W/m2. [ABSTRACT FROM AUTHOR]

Black carbon in snow (BCS) has a significant impact on global climate and is an important component of Earth system modeling. Here, we provide a comprehensive evaluation of BCS simulations in the Coupled Model Intercomparison Project Phase 6 (CMIP6) and its radiative forcing on a global scale. Overall, the multi-model mean generally captures the characteristics of BCS spatial patterns, with maximum concentrations in East Asia and the Tibetan Plateau (~120 ng·g−1), and the lowest in Antarctica (~0.05 ng·g−1). The BCS concentrations in all CMIP6 multi-model mean and individual models generally exhibit a temporally increasing trend globally, with particularly large increases after the 1940s. In terms of seasonal cycles, individual models are generally consistent in most regions. Globally, BCS concentrations are highest around January and lowest in September. The albedo reduction in the Tibetan Plateau and East Asia simulated by the CMIP6 multi-model mean reached ~0.06 in 2014 and may influence climate more than expected. [ABSTRACT FROM AUTHOR]

The Pan‐Third Pole contains the largest number of glaciers outside the polar region that plays a crucial role in atmospheric circulation and the hydrological cycle. However, this pristine region has undergone rapid change through complex interactions including the black carbon (BC) enhanced warming effect and glacier melting. Study shows, Weather Research and Forecasting coupled with Chemistry (WRF‐Chem) simulation is able to capture distinctive seasonal variability of BC. The result from our sensitivity experiments revealed that South Asia (SA; 60.7%) and East Asia (EA; 32.9%) contributed more toward the Tibetan Plateau (TP). Our analysis on aerosol‐boundary feedback interaction revealed BC expand planetary boundary layer height by 5.0% and 4.8% over SA and EA, respectively, which facilitates BC dispersion and transportation. Whereas, we also found that under the influence of different wind regimes the significant BC transport flux aloft over the TP and the upper troposphere and lower stratosphere. Additionally, mountain‐valley channel and synoptic and local meteorological processes also facilitated BC transport to the TP. This study also evaluated the effect of BC on direct radiative forcing and calculated subsequent temperature changes. A strong dimming effect of BC corroborated with the following negative surface temperature changes. However, enhanced BC concentration during winter and spring caused the increase in temperature over the TP. Here, the WRF‐Chem model, synergy on aerosol‐boundary feedback, BC transport flux, and source‐receptor methods confirmed the significant BC contribution and transportation, and notable BC‐induced warming over TP. Such trans‐Himalayan BC transport and associated warming could grim glacier melt and water availability in the region. Key Points: Trans‐Himalaya long‐range transport is evident with significant black carbon (BC) transport flux aloft above Himalayas and Tibetan Plateau and free troposphere from South Asia (SA) and East Asia (EA) regionSynergy on aerosol‐boundary feedback interaction manifested that BC expand planetary boundary layer height by 5.01% and 4.80% over SA and EA, respectivelyElevated BC caused notable warming over Tibetan Plateau that could pose a threat in the cryosphere over that region [ABSTRACT FROM AUTHOR]

Studies of the climate effects of black carbon (BC) in East Asia are not abundant and the effects remain uncertain. Using the Community Earth System Model version 1 (CESM1) with Peking University's emissions data, the fast response of the atmospheric water cycle to anthropogenic BC during summer in East Asia is investigated in this study. Results show that the CESM1-simulated BC concentration and its direct effective radiative forcing are comparable to observations. With the combination of aerosol–radiation interaction (ARI) and non-aerosol–radiation interaction (including aerosol–cloud interaction and surface albedo effects), anthropogenic BC induces a "wetter south and drier north" pattern over East Asia during summer. Also, anthropogenic BC affects the summer precipitation primarily through changing moisture transport rather than altering local evaporation over East Asia. Using the self-developed atmospheric water tracer method, the responses of dominant moisture sources [the tropical Indian Ocean (TIO) and northwest Pacific] to anthropogenic BC are investigated. Results show that the moisture originating from southwest monsoon-related sources (especially the TIO) is more responsive to anthropogenic BC effects over East Asia. In particular, differing from total precipitation, TIO-supplied precipitation shows a significant response to the ARI of anthropogenic BC over East Asia. Process analyses show that anthropogenic BC affects the southwest monsoon-related moisture supplies primarily via advection, deep convection, and cloud macrophysics. Interestingly, the anthropogenic BC-induced changes of TIO-supplied water vapor in these three processes are all dominated by the ARI over East Asia. [ABSTRACT FROM AUTHOR]

Black carbon (BC) aerosol is a significant and short-lived climate forcing factor. Here, the direct effects of BC emissions from India (IDBC) and China (CNBC) are investigated in East Asia during summer using the state-of-the-art regional climate model RegCM4. In summer, IDBC and CNBC account for approximately 30% and 46% of the total BC emissions in Asia, respectively. The total BC column burden from the two countries and corresponding TOA effective radiative forcing are 1.58 mgm-2 and 11.87Wm-2 in East Asia, respectively. The regional air temperature increases over 0.3K at maximum and precipitation decreases 0.028mmday-1 on average. Individually, IDBC and CNBC each can bring about rather different effects on regional climate. IDBC can result in a cooling perturbation accompanied by a substantially increased cloud amount and scattering aerosol loading, resulting in a complex response in the regional precipitation, while CNBC can lead to regional warming, and further induce a local flood in northern China or drought in southern China depending on the opposite but significant circulation anomalies. CNBC plays a dominant role in modulating the regional climate over East Asia due to its higher magnitude, wider coverage, and stronger climate feedback. The direct effect of the total BC from both countries is not a linear combination of that of IDBC and CNBC individually, suggesting that the regional climate responses are highly nonlinear to the emission intensity or aerosol loading, which may be greatly related to the influences of the perturbed atmospheric circulations and climate feedback. [ABSTRACT FROM AUTHOR]

Understanding the global distribution of atmospheric black carbon (BC) is essential for unveiling its climatic effect. However, there are still large uncertainties regarding the simulation of BC transport due to inadequate information about the removal process. We accessed the wet removal rate of BC in East Asia based on long-term measurements over the 2010–2016 period at three representative background sites (Baengnyeong and Gosan in South Korea and Noto in Japan). The average wet removal rate, represented by transport efficiency (TE), i.e., the fraction of undeposited BC particles during transport, was estimated to be 0.73 in East Asia from 2010 to 2016. According to the relationship between accumulated precipitation along trajectory and TE, the wet removal efficiency was lower in East and North China but higher in South Korea and Japan, implying the importance of the aging process and frequency of exposure to below- and in-cloud scavenging conditions during air mass transport. Moreover, the wet scavenging in winter and summer showed the highest and lowest efficiency, respectively, although the lowest removal efficiency in summer was primarily associated with a reduced BC aging process because the in-cloud scavenging condition was dominant. The average half-life and e -folding lifetime of BC were 2.8 and 7.1 d , respectively, which is similar to previous studies, but those values differed according to the geographical location and meteorological conditions of each site. Next, by comparing TE from the FLEXible PARTicle (FLEXPART) Lagrangian transport model (version 10.4), we diagnosed the scavenging coefficients (s -1) of the below- and in-cloud scavenging scheme implemented in FLEXPART. The overall median TE from FLEXPART (0.91) was overestimated compared to the measured value, implying the underestimation of wet scavenging coefficients in the model simulation. The median of the measured below-cloud scavenging coefficient showed a lower value than that calculated according to FLEXPART scheme by a factor of 1.7. On the other hand, the overall median of the calculated in-cloud scavenging coefficients from the FLEXPART scheme was highly underestimated by 1 order of magnitude, compared to the measured value. From an analysis of artificial neural networks, the convective available potential energy, which is well known as an indicator of vertical instability, should be considered in the in-cloud scavenging process to improve the representative regional difference in BC wet scavenging over East Asia. For the first time, this study suggests an effective and straightforward evaluation method for wet scavenging schemes (both below and in cloud), by introducing TE along with excluding effects from the inaccurate emission inventories. [ABSTRACT FROM AUTHOR]

Atmospheric black carbon (BC) in the Tibetan Plateau (TP) can largely impact regional and global climate. Still, studies on the inter-annual variation in atmospheric BC over the TP and associated variation in BC sources and controlling factors are rather limited. In this study, we characterize the variations in atmospheric BC over the TP surface layer through analysis of 20-year (1995–2014) simulations from a global chemical transport model, GEOS-Chem. The results show that surface BC concentrations over the TP vary largely in space and by season, reflecting complicated interplays of BC sources from different origins. Of all areas in the TP, surface BC concentrations are highest over the eastern and southern TP, where surface BC is susceptible to BC transport from East Asia and South Asia, respectively. Applying a backward-trajectory method that combines BC concentrations from GEOS-Chem and trajectories from the Hybrid Single-Particle Lagrangian Integrated Trajectory (HYSPLIT) model, we assess the contributions of worldwide source regions to surface BC in the TP. We estimate that on the 20-year average, 77 % of surface BC in the TP comes from South Asia (43 %) and East Asia (35 %). Regarding seasonal variation in non-local influences, South Asia and East Asia are dominant source regions in winter and summer, respectively, in terms of the amount of BC imported. However, in terms of affected areas in the TP, South Asia is the dominant contributor throughout the year. Inter-annually, surface BC over the TP is largely modulated by atmospheric transport of BC from non-local regions year-round and by biomass burning in South Asia, mostly in spring. We find that the extremely strong biomass burning in South Asia in the spring of 1999 greatly enhanced surface BC concentrations in the TP (31 % relative to the climatology). We find that the strength of the Asian monsoon correlates significantly with the inter-annual variation in the amount of BC transported to the TP from non-local regions. In summer, a stronger East Asian summer monsoon and a stronger South Asian summer monsoon tend to, respectively, lead to more BC transport from central China and north-eastern South Asia to the TP. In winter, BC transport from central China is enhanced in years with a strong East Asian winter monsoon or a strong Siberian High. A stronger Siberian High can also bring more BC from northern South Asia to the TP. This study underscores the impacts of atmospheric transport and biomass burning on the inter-annual variation in surface BC over the TP. It reveals a close connection between the Asian monsoon and atmospheric transport of BC from non-local regions to the TP. [ABSTRACT FROM AUTHOR]

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. [ABSTRACT FROM AUTHOR]

Black carbon (BC) aerosol is a significant, short-lived climate forcing agent. To further understand the effects of BCs on the regional climate, the warming effects of BCs from residential, industrial, power and transportation emissions are investigated in Asian regions during summer using the state-of-the-art regional climate model RegCM4. BC emissions from these four sectors have very different rates and variations. Residential and industrial BCs account for approximately 85% of total BC emissions, while power BCs account for only approximately 0.19% in Asian regions during summer. An investigation suggests that both the BC aerosol optical depth (AOD) and direct radiative forcing (DRF) are highly dependent on emissions, while the climate effects show substantial nonlinearity to emissions. The total BCs AOD and clear-sky top of the atmosphere DRF averaged over East Asia (100–130°E, 20–50°N) are 0.02 and + 1.34 W/m2, respectively, during summer. Each sector's BC emissions may result in a warming effect over the region, leading to an enhanced summer monsoon circulation and a subsequent local decrease (e.g., northeast China) or increase (e.g., south China) in rainfall in China and its surrounding regions. The near surface air temperature increased by 0.2 K, and the precipitation decreased by approximately 0.01 mm/day in east China due to the total BC emissions. The regional responses to the BC warming effects are highly nonlinear to the emissions, which may be linked to the influences of the perturbed atmospheric circulations and climate feedback. The nonuniformity of the spatial distribution of BC emissions may also have significant influences on climate responses, especially in south and east China. The results of this study could aid us in better understanding BC effects under different emission conditions and provide a scientific reference for developing a better BC reduction strategy over Asian regions. [ABSTRACT FROM AUTHOR]

In this study, we estimated the contribution of black carbon (BC) and brown carbon (BrC) to aerosol light absorption from surface in-situ and aerosol robotic network (AERONET) columnar observations. The mass absorption cross-section (MAC) of BC ( MAC BC ) was estimated to be 6.4 ± 1.5 m2 g−1 at 565 nm from in-situ aerosol measurements at Gosan Climate Observatory (GCO), Korea, in January 2014, which was lower than those observed in polluted urban areas. A BrC MAC of 0.62 ± 0.06 m2 g−1 (565 nm) in our estimate is approximately ten times lower than MAC BC at 565 nm. The contribution of BC and BrC to the carbonaceous aerosol absorption coefficient at 565 nm from the in-situ measurements was estimated at 88.1 ± 7.4% and 11.9 ± 7.4%, respectively at GCO. Similarly, the contribution of BC and BrC to the absorption aerosol optical depth (AAOD) for carbonaceous aerosol (CA), constrained by AERONET observations at 14 sites over East Asia by using different spectral dependences of the absorption (i.e., absorption Ångström exponent) of BC and BrC, was 84.9 ± 2.8% and 15.1 ± 2.8% at 565 nm, respectively. The contribution of BC to CA AAOD was greater in urban sites than in the background areas, whereas the contribution of BrC to CA AAOD was higher in background sites. The overall contribution of BC to CA AAOD decreased by 73%–87% at 365 nm, and increased to 93%–97% at 860 nm. The contribution of BrC to CA AAOD decreased significantly with increasing wavelength from approximately 17% at 365 nm to 4% at 860 nm. • We estimated the contribution of black carbon (BC) and brown carbon (BrC) to aerosol light absorption. • We used surface in-situ and column AERONET data from Gosan in January 2014. • The contribution of BC and BrC at 565 nm was estimated at 88.1±7.4% and 11.9±7.4%. • The contribution of BC and BrC to AAOD was 84.9±2.8% and 15.1±2.8%, respectively. • The contribution of BC to CA AAOD was greater in urban sites than in the background areas, whereas the contribution of BrC to CA AAOD was higher in background sites. [ABSTRACT FROM AUTHOR]

Long-term measurements of black carbon (BC) aerosols by filter-based absorption photometers with a heated inlet (COSMOS) in different regions have been useful in elucidating spatial variations and radiative impacts of BC. Evaluations of mass concentrations of BC (MBC) measured by the COSMOS have been made by our previous studies through comparisons with other measurement techniques. However, how variations in the microphysical properties of BC and the co-existing light scattering aerosols affect the COSMOS measurements should be evaluated in more detail. In this study, we assessed these potential effects under various field environments in the Arctic and in the East Asia. From the slopes of the correlation plots between the MBC values measured by the COSMOS and a single-particle soot photometer, the average accuracy of the COSMOS was estimated as ∼10% in the MBC range 1–3000 ng m−3. On an hourly basis, the estimated sensitivity of the COSMOS MBC values to the changes in the BC size distributions was less than 10%, within the typical variabilities of BC size at individual observation sites. The COSMOS measurements depended little on the mixing states of BC and the concentrations of co-existing light scattering aerosols, except in the maritime air masses of East Asia, where the relative abundance of sea salt to BC was very high. The MBC measured by COSMOS also well agreed with elemental carbon measurements. Our results demonstrate the high reliability of COSMOS measurements under various environments. Copyright © 2019 American Association for Aerosol Research [ABSTRACT FROM AUTHOR]

Lulin Atmospheric Background Station (LABS, 23.47°N, 120.87°E; 2862 m above sea level) at the summit of Mount Lulin in central Taiwan was established in spring 2006 and is the only high-altitude background station over western Pacific region in East Asia to study the impact of various air pollutants through long-range transport. Continuous in-situ measurements of equivalent black carbon (EBC) and carbon monoxide (CO) concentrations were made at LABS from June 2012 to May 2014 and their association was investigated in this study. The highest monthly concentration of EBC (median; 840 ng m−3) and CO (212 ppbv) in March were primarily attributed to the westerly winds coupled with biomass-burning (BB) emissions from Southeast Asia (SEA) region. The association of EBC and CO was weak at LABS possibly due to the influence of dissimilar air masses from various sources, and scavenging or dilution of EBC during the long-range atmospheric transport to Mt. Lulin. The mean ΔEBC/ΔCO ratio (slope of least-squares regression line of ΔEBC-ΔCO scatterplot; where Δ indicates surplus amounts with respect to the background value) was found the most significant in March (5.3 ng m−3 ppbv−1 or 7.3 × 10−3 g of carbon as EBC per gram of carbon as CO). On the basis of episodic cases, the mean ΔEBC/ΔCO ratios at LABS were estimated to be 6.1, 8.0, and 2.4 ng m−3 ppbv−1 for SEA BB emissions, southern China mixed pollution, and northern China mixed pollution, respectively. A total of 32% loss in EBC aerosols (6.4% of EBC removal per day) was estimated for the atmospheric transport of BB emissions from SEA region to LABS. This study provides needful information to understand the ΔEBC/ΔCO ratios at a remote site and would be used in model simulations to evaluate BC aging and scavenging over western Pacific region in East Asia. • First attempt of ΔEBC/ΔCO ratio investigation at Mt. Lulin. • Annual EBC concentration was found comparable with other high altitude locations. • Peaks in EBC, CO, and ΔEBC/ΔCO were observed in March attributed to BB emissions from Southeast Asia. [ABSTRACT FROM AUTHOR]

The emergence and expansion of terrestrial C 4 vegetation represent the most striking evolutionary adaptation of ecosystems to climate change during the Cenozoic. However, the long-term history of terrestrial C 4 ecosystem expansion in East Asia remains poorly documented, and its links to tectonic and/or climate changes remain unclear due to the complexity of its forcing factors. Here, we reconstruct the long-term evolution of terrestrial C 3 –C 4 plants biomass in South China since the late Eocene using continuous records of the stable carbon isotopic compositions (δ13C) of black carbon extracted from sediments at International Ocean Discovery Program (IODP) Site U1501 in the northern South China Sea (SCS). This study reveals remarkable stepwise expansions of C 4 plants in South China at ∼20 Ma and 15 Ma with a gradual expansion trend at 7–4 Ma. We demonstrate that stepwise drying (long-term weakening of the East Asian summer monsoon and simultaneous strengthening of the East Asian winter monsoon), as well as the enhanced seasonality of precipitation, is responsible for the ecological evolution in South China since the early Miocene. Our black carbon records, combined with previous studies, indicate a coupled evolution of East Asian drying, vegetation shifts and global cooling. We suggest that the major Asian topography framework was established before the middle Miocene, and global cooling overwhelmed tectonic controls of the long-term evolution of the East Asian monsoon thereafter. This study highlights that both Tibetan uplift and global cooling have played a significant role in the long-term evolution of regional climate and vegetation. • Stepwise expansion of C 4 plant in South China occurred at 20 Ma, 15 Ma and 7–4 Ma. • Stepwise drying and enhanced seasonality of precipitation induced C 4 plant expansion in South China. • Both Tibetan uplift and global cooling played a significant role in evolution of East Asian monsoon. [ABSTRACT FROM AUTHOR]

We analyzed annual and seasonal frequency in aerosol type over an 8-year period (2012–2019) to identify aerosol parameter trends over four ground sites and country regions in Korea, China, and Japan by using the Aerosol Robotic Network (AERONET), and the satellite-based Visible Infrared Imaging Radiometer Suite (VIIRS) and Ozone Monitoring Instrument (OMI). Decreasing trends are shown for aerosol optical depth (AOD), Ångström exponent (AE), and fine mode fraction (FMF) in all countries. The decreasing trend in these data is considered to be due to a decrease in anthropogenic emissions. For the aerosol type frequency, decreases in the proportions of carbonaceous aerosols (CA) and non-absorbing aerosols (NA) were shown in the ground and satellite data, respectively. At most sites, the fractions of low AOD case (LOW) increased, whereas those of the Black and Brown Carbon (BC + BrC) category decreased. In Seoul, the fraction of LOW increased from 48.9% to 70.0%, and that of BC + BrC decreased continuously from 20.4% to 11.1% during 2012–2019. Beijing, on the other hand, showed decreasing LOW from 83.3% (2012) to 52.0% (2019), and that of BC + BrC increased significantly, from 2.4% to 26.2%. The satellite data showed that the percentage of LOW increased continuously, while that of NA aerosols decreased continuously in East Asia. A noticeable decrease in the fraction of CA was detected in China [21.5% (2013) to 11.2% (2019)]. In all countries, CA and NA aerosols had the greatest effect in winter and summer, respectively. We also detected significant differences between the fractions of NA and BC between the ground and satellite data. Changes in aerosol type and properties were observed concurrently in all ground and satellite data, and changes in aerosol type may explain the increasing and decreasing trends that we recorded for most parameters. Consistent results from both ground and satellite data suggest a steady decreasing in fine aerosol pollution in East Asia. • Comparison of long-term aerosol parameter trends and type changes using both ground and satellite data • Aerosol type determination using modified criteria and weighting method for aerosol parameters • Trends of aerosol types shows decreasing effect of high-level pollution during 2012–2019. • Significant frequency changes of 'non-absorbing' aerosol types and low AOD cases especially in satellite data [ABSTRACT FROM AUTHOR]

The spatiotemporal characteristics of aerosol direct radiative forcing (RF) and the relative contributions from aerosol species, as well as the impacts of cloud coverage and relative humidity on aerosol direct RF were quantified in East Asia using a regional climate model. Generally, the total aerosol produces net RFs of −12.78 W m−2 at surface, 1.72 W m−2 at TOA (top-of-atmosphere), and atmospheric heating of 14.50 W m−2. It was found that dust, black carbon, and sulfate made dominant contributions to the total RF at surface and TOA, and all aerosol species induced atmospheric heating, whereas more than 96% of which was induced by dust and black carbon. The remarkably seasonally decreasing tendency of the total and the absorbing aerosol RFs was found from spring to winter at surface. Moreover, dust contributes relatively larger to the positive TOA RF and to the atmospheric heating in spring and summer, which were weakened and smaller than black carbon in other seasons. Sensitivity studies further demonstrated cloud strengthens the dust and black carbon direct RF and weakens the other species direct RF at TOA, while induces weak direct RFs of all aerosol species at surface. Particularly, cloud induced larger reduction in dust longwave RF than shortwave leads to remarkable enhanced net surface direct RF of dust, especially in JJA. The aerosol swelling effect induced by relative humidity strengthens aerosol direct RF at both TOA and surface. The percentage changes in aerosol RF and its seasonal amplitude by cloud are considered larger at TOA than surface, however, the effects of relative humidity distribute relatively uniform vertically. Meteorological factors impact on scattering aerosols direct RF is assumed larger than absorbing aerosols. The impacts of cloud on aerosol direct RF are compared to the relative humidity and are supposed to be more important at TOA and surface. • Contributions and seasonal trends of different aerosol direct RF are studied. • Different aerosol direct RFs respond obviously different to the presence of cloud. • Larger loss of dust LW RF than SW by cloud induces enhanced net RF at surface in JJA. • Water vapor strengthens each type of aerosol direct RF at both TOA and surface. • Aerosol direct RF is more sensitive to cloud conditions than relative humidity. [ABSTRACT FROM AUTHOR]

Black carbon (BC) exerts potential effect on climate, especially in the Tibetan Plateau (TP), where the cryosphere and environment are very sensitive to climate change. Although transport of atmospheric BC from South and East Asia to the TP has been comprehensively investigated, transport of BC from Central and West Asia (CWA) to the TP and its climate effect on the region have received little attention and are warrant investigation. Therefore, based on the observation and ERA-Interim reanalysis data, this study investigated transport of atmospheric BC from CWA to the TP, its seasonality and climate effect over the TP using WRF-Chem model. On an annual scale, BC from CWA contributes to 5.8% of total BC over the TP. Seasonally, the contribution rates were 5.1%, 5.9%, 6.2%, and 5.7% in spring, summer, autumn, and winter, respectively. The area-averaged surface radiative forcing over the TP induced by BC from CWA ranged from −0.14 to −0.04 W m−2, with the largest and smallest negative radiative forcing occurring in autumn and winter, respectively. Affected by BC from CWA, the area-averaged surface temperature over the TP increased by 0.033 °C in summer, whereas it decreased by 0.002, 0.005, and 0.001 °C in spring, autumn and winter, respectively. In the atmosphere over the TP, the positive radiative forcing with values of 0.17, 0.20, 0.04, and 0.07 W m−2 were induced by BC from CWA in spring, summer, autumn, and winter, respectively. At the top of the atmosphere over the TP, the calculated radiative forcing associated with BC from CWA were 0.08, 0.14, −0.1, and 0.03 W m−2 in spring, summer, autumn, and winter, respectively. On an annual scale, the radiative forcing in the atmosphere and at the top of the atmosphere over the TP caused by BC from CWA were 0.12 W m−2 and 0.04 W m−2, respectively. This study enriched the theoretical connotation of transboundary transport of BC aerosols to the TP. [Display omitted] • Central-west Asian (CWA) black carbon (BC) contributes to 5.8% of BC in the TP. • Radiative forcing on the TP induced by BC from CWA ranged from −0.14 to −0.04 W m−2. • Affected by BC from CWA, surface temperature on the TP increased in summer and decreased in other seasons. [ABSTRACT FROM AUTHOR]

[Display omitted] Chronic exposure to fine particulate matter (PM 2. 5) poses a major global health risk, commonly assessed by assuming equivalent toxicity for different PM 2. 5 constituents. We used a data-informed global atmospheric model and recent exposure–response functions to calculate the health burden of ambient PM 2. 5 from ten source categories. We estimate 4.23 (95% confidence interval 3.0–6.14) million excess deaths annually from the exposure to ambient PM 2. 5. We distinguished contributions and major sources of black carbon (BC), primary organic aerosols (POA) and anthropogenic secondary organic aerosols (aSOA). These components make up to ∼20% of the total PM 2. 5 in South and East Asia and East Africa. We find that domestic energy use by the burning of solid biofuels is the largest contributor to ambient BC, POA and aSOA globally. Epidemiological and toxicological studies indicate that these compounds may be relatively more hazardous than other PM 2. 5 compounds such as soluble salts, related to their high potential to inflict oxidative stress. We performed sensitivity analyses by considering these species to be more harmful compared to other compounds in PM 2.5 , as suggested by their oxidative potential using a range of potential relative risks. These analyses show that domestic energy use emerges as the leading cause of excess mortality attributable to ambient PM 2. 5 , notably in Asia and Africa. We acknowledge the uncertainties inherent in our assumed enhanced toxicity of the anthropogenic organic and BC aerosol components, which suggest the need to better understand the mechanisms and magnitude of the associated health risks and the consequences for regulatory policies. However our assessment of the importance of emissions from domestic energy use as a cause of premature mortality is robust to a range of assumptions about the magnitude of the excess risk. [ABSTRACT FROM AUTHOR]

An interactive system coupling the Beijing Climate Center atmospheric general circulation model (BCC_AGCM2.0.1) and the Canadian Aerosol Module (CAM) with updated aerosol emission sources was developed to investigate the global distributions of optical properties and direct radiative forcing (DRF) of typical aerosols and their impacts on East Asian climate. The simulated total aerosol optical depth (AOD), single scattering albedo, and asymmetry parameter were generally consistent with the ground-based measurements. Under all-sky conditions, the simulated global annual mean DRF at the top of the atmosphere was −2.03 W m for all aerosols including sulfate, organic carbon (OC), black carbon (BC), dust, and sea salt; the global annual mean DRF was −0.23 W m for sulfate, BC, and OC aerosols. The sulfate, BC, and OC aerosols led to decreases of 0.58° and 0.14 mm day in the JJA means of surface temperature and precipitation rate in East Asia. The differences of land-sea surface temperature and surface pressure were reduced in East Asian monsoon region due to these aerosols, thus leading to the weakening of East Asian summer monsoon. Atmospheric dynamic and thermodynamic were affected due to the three types of aerosol, and the southward motion between 15°N and 30°N in lower troposphere was increased, which slowed down the northward transport of moist air carried by the East Asian summer monsoon, and moreover decreased the summer monsoon precipitation in south and east China. [ABSTRACT FROM AUTHOR]

Abstract: Carbonaceous aerosol is one of the main ingredients of the atmospheric aerosol, which includes black carbon and organic carbon. The numerical simulations from 1960 to 2000 are aimed at the direct radiative effects on climate induced by carbonaceous aerosol in East Asia using NCAR Community Atmospheric Model version 3.1 (CAM). The mean radiative forcing(RF) under all sky in Chinese mainland at TOA and surface are 0.38 and −5.31W/m2 respectively. This distinct RF leads to −0.1K surface temperature decrease in Chinese mainland, which includes −0.26K drop of daily maximum and 0.07K rise of minimum temperature. Air column temperature has also been increased 0.11K in Chinese mainland. Significant vapor and precipitation increase can be resulted from RF of carbonaceous aerosol in north China and the Yellow and Huai River basin, accompanied by the decrease in northeast China, far-east region, and Tibet Plateau. [Copyright &y& Elsevier]

The results from studies of aerosol in the Arctic atmosphere are presented: the aerosol optical depth (AOD), the concentrations of aerosol and black carbon, as well as the chemical composition of the aerosol. The average aerosol characteristics, measured during nine expeditions (2007–2018) in the Eurasian sector of the Arctic Ocean, had been 0.068 for AOD (0.5 µm); 2.95 cm−3 for particle number concentrations; 32.1 ng/m3 for black carbon mass concentrations. Approximately two–fold decrease of the average characteristics in the eastern direction (from the Barents Sea to Chukchi Sea) is revealed in aerosol spatial distribution. The average aerosol characteristics over the Barents Sea decrease in the northern direction: black carbon concentrations by a factor of 1.5; particle concentrations by a factor of 3.7. These features of the spatial distribution are caused mainly by changes in the content of fine aerosol, namely: by outflows of smokes from forest fires and anthropogenic aerosol. We considered separately the measurements of aerosol characteristics during two expeditions in 2019: in the north of the Barents Sea (April) and along the Northern Sea Route (July–September). In the second expedition the average aerosol characteristics turned out to be larger than multiyear values: AOD reached 0.36, particle concentration up to 8.6 cm−3, and black carbon concentration up to 179 ng/m3. The increased aerosol content was affected by frequent outflows of smoke from forest fires. The main (99%) contribution to the elemental composition of aerosol in the study regions was due to Ca, K, Fe, Zn, Br, Ni, Cu, Mn, and Sr. The spatial distribution of the chemical composition of aerosols was analogous to that of microphysical characteristics. The lowest concentrations of organic and elemental carbon (OC, EC) and of most elements are observed in April in the north of the Barents Sea, and the maximal concentrations in Far East seas and in the south of the Barents Sea. The average contents of carbon in aerosol over seas of the Asian sector of the Arctic Ocean are OC = 629 ng/m3, EC = 47 ng/m3. [ABSTRACT FROM AUTHOR]

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. [ABSTRACT FROM AUTHOR]

Although some studies reported the impact of black carbon (BC) on the climate over the Tibetan Plateau (TP), the contribution and mechanisms of BC affecting the water vapor transport to Tibet are not fully understood yet. Here, utilizing the satellite observations and reanalysis data, the effects of BC on the climate over the TP and water vapor transport to the Tibet were investigated by the Community Earth System Model (CESM 2.1.0). Due to the addition of BC, a positive net heat forcing (average is 0.39 W/m2) is exerted at the surface, which induces a pronounced warming effect over the TP and consequently intensifies the East Asian Summer monsoon (EASM). However, significant cooling effects in northern India, Pakistan, Afghanistan and Iran are induced due to the BC and related feedbacks, which reduces significantly the meridional land–sea thermal contrast and finally weakens the South Asian summer monsoon (SASM). Consequently, the water vapor transport to the south border will be decreased due to addition of BC. Moreover, through affecting the atmospheric circulation, the BC could induce an increase in the imported water vapor from the west and east borders of the TP, and an increase outflowing away from the north border of the TP. Overall, due to the BC, the annual mean net importing water vapor over TP is around 271 Gt, which could enhance the precipitation over the TP. The results show that the mean increase in the precipitation over TP is about 0.56 mm/day. [ABSTRACT FROM AUTHOR]