Refractory black carbon (rBC) is a primary aerosol species, produced through incomplete combustion, that absorbs sunlight and contributes to positive radiative forcing. The overall climate effect of rBC depends on its spatial distribution and atmospheric lifetime, both of which are impacted by the efficiency with which rBC is transported or removed by convective systems. These processes are poorly constrained by observations. It is especially interesting to investigate rBC transport efficiency through the Asian Summer Monsoon (ASM) since this meteorological pattern delivers vast quantities of boundary layer air from Asia, where rBC emissions are high to the upper troposphere/lower stratosphere (UT/LS) where the lifetime of rBC is expected to be long. Here, we present in situ observations of rBC made during the Asian Summer Monsoon Chemistry and Climate Impact Project of summer, 2022. We use observed relationships between rBC and CO in ASM outflow to show that rBC is removed nearly completely (>98%) from uplifted air and that rBC concentrations in ASM outflow are statistically indistinguishable from the UT/LS background. We compare observed rBC and CO concentrations to those expected based on two chemical transport models and find that the models reproduce CO to within a factor of 2 at all altitudes whereas rBC is overpredicted by a factor of 20-100 at altitudes associated with ASM outflow. We find that the rBC particles in recently convected air have thinner coatings than those found in the UTLS background, suggesting transport of a small number of rBC particles that are negligible for concentration.

Rainfall can alter the hydrothermal state of permafrost, subsequently affecting organic carbon decomposition and CO2 transport. However, the mechanisms by which rainfall influences organic carbon decomposition and carbon dioxide transport processes in permafrost remain unclear. In this study, a coupled permafrost water-heatvapor-carbon model, based on the surface energy-water balance theory, is employed to explore the effects of increased precipitation on permafrost moisture, temperature, organic carbon decomposition, and carbon dioxide transport through numerical simulations. The results are as follows: (1) with increased rainfall, surface latent heat flux rises while surface sensible heat flux declines, leading to a reduction in surface heat flux. The annual mean surface heat fluxes for the three precipitation conditions of no change in precipitation (zP = 0 mm), 50 mm increase in precipitation (zP = 50 mm) and 100 mm increase in precipitation (zP = 100 mm) are -0.1 W/m2, -0.2 W/m2 and -0.4 W/m2 respectively; and (2) as rainfall increases, soil moisture content increases significantly, but the impact of rainfall on soil moisture content diminishes with increasing soil depth; and (3) increased rainfall results in a decrease in soil carbon fluxes, soil organic matter decomposition rates, and CO2 concentrations. Compared to the case of constant precipitation, the surface carbon fluxes decreased by 0.04 mu mol center dot m-2s-1 and 0.08 mu mol center dot m-2s-1 under zP = 50 mm and zP = 100 mm, respectively. Additionally, the decomposition rate of soil organic matter at 10 cm depth decreased by 3.2 E-8 mol center dot m-2s-1 and 6.3 E-8 mol center dot m-2s-1, respectively, while the soil carbon concentration decreased by 3 mu mol/mol and 5 mu mol/mol, respectively.

1. Phosphorous (P) is essential for mediating plant and microbial growth and thus could impact carbon (C) cycle in permafrost ecosystem. However, little is known about soil P availability and its biological acquisition strategies in permafrost environment. 2. Based on a large-scale survey along a similar to 1000 km transect, combining with shotgun metagenomics, we provided the first attempt to explore soil microbial P acquisition strategies across the Tibetan alpine permafrost region. 3. Our results showed the widespread existence of microbial functional genes associated with inorganic P solubilization, organic P mineralization and transportation, reflecting divergent microbial P acquisition strategies in permafrost regions. Moreover, the higher gene abundance related to solubilization and mineralization as well as an increased ration of metagenomic assembled genomes (MAGs) carrying these genes were detected in the active layer, while the greater abundance of low-affinity transporter gene (pit) and proportions of MAGs harbouring pit gene were observed in permafrost deposits, illustrating a stronger potential for P activation in active layer but an enhanced P transportation potential in permafrost deposits. 4. Our results highlight multiple P-related acquisition strategies and their differences among various soil layers should be considered simultaneously to improve model prediction for the responses of biogeochemical cycles in permafrost ecosystems to climate change.

The transboundary mercury (Hg) pollution has caused adverse effects on fragile ecosystems of the Tibetan Plateau (TP). Yet, knowledge of transport paths and source regions of atmospheric Hg on the inland TP remains poor. Continuous measurements of atmospheric total gaseous mercury (TGM) were conducted in the central TP (Tanggula station, 5100 m a.s.l., June -October). Atmospheric TGM level at Tanggula station (1.90 +/- 0.30 ng m -3 ) was higher than the background level in the Northern Hemisphere. The identified high -potential source regions of atmospheric TGM were primarily located in the northern South Asia region. TGM concentrations were lower during the Indian summer monsoon (ISM) -dominant period (1.81 +/- 0.25 ng m -3 ) than those of the westerly -receding period (2.18 +/- 0.40 ng m -3 ) and westerly -intensifying period (1.91 +/- 0.26 ng m -3 ), contrary to the seasonal pattern in southern TP. The distinct TGM minima during the ISM -dominant period indicated lesser importance of ISM -transported Hg to Tanggula station located in the northern boundary of ISM intrusion, compared to stations in proximity to South and Southeast Asia source regions. Instead, from the ISM -dominant period to the westerly -intensifying period, TGM concentrations showed an increasing trend as westerlies intensified, indicating the key role of westerlies in transboundary transport of atmospheric Hg to the inland TP.

South and Southeast Asia (SSA) emitted black carbon (BC) exerts potential effects on glacier and snow melting and regional climate change in the Tibetan Plateau. In this study, online BC measurements were conducted for 1 year at a remote village located at the terminus of the Mingyong Glacier below the Meili Snow Mountains. The Weather Research and Forecasting model coupled with Chemistry (WRF-Chem) was used to investigate the contribution and potential effect of SSA -emitted BC. In addition, variations in the light absorption characteristics of BC and brown carbon (BrC) were examined. The results indicated that the annual mean concentration of BC was 415 +/- 372 ngm(-3) , with the highest concentration observed in April (monthly mean: 930 +/- 484 ngm(-3) ). BC exhibited a similar diurnal variation throughout the year, with two peaks observed in the morning (from 8:00 to 9:00 AM) and in the afternoon (from 4:00 to 5:00 PM), with even lower values at nighttime. At a short wavelength of 370 nm, the absorption coefficient ( b abs ) reached its maximum value, and the majority of b abs values were < 20 Mm(-1) , indicating that the atmosphere was not overloaded with BC. At the same wavelength, BrC substantially contributed to b abs , with an annual mean of 25.2 % +/- 12.8 %. SSA was the largest contributor of BC (annual mean: 51.1 %) in the study area, particularly in spring (65.6 %). However, its contributions reached 20.2 % in summer, indicating non -negligible emissions from activities in other regions. In the atmosphere, the SSA BC -induced radiative forcing (RF) over the study region was positive. While at the near surface, the RF exhibited a significant seasonal variation, with the larger RF values occurring in winter and spring. Overall, our findings highlight the importance of controlling BC emissions from SSA to protect the Tibetan Plateau against pollution -related glacier and snow cover melting.

Understanding the origins of Tibetan Plateau (TP) glacier dust is vital for glacier dynamics and regional climate understanding. In May 2016, snow pit samples were collected from glaciers on the TP: Qiyi (QY) in the north, Yuzhufeng (YZF) in the center, and Xiaodongkemadi (XDK) in the south. Rare earth element (REE) concentrations were analyzed using inductively coupled plasma mass spectrometry (ICP-MS), and near-surface PM10 concentrations were extracted from a dataset of Chinese near-surface PM10. Two tracing approaches were used: direct REE tracing and an indirect approach combining potential source contribution function (PSCF) and concentration-weighted trajectory (CWT). Both methods yielded consistent results. Pre-monsoon, TP surface soils, Taklimakan Desert, and Qaidam Basin contributed to glacier dust. Notably, central and southern glaciers showed Thar Desert influence, unlike the northern ones. Taklimakan and Thar Deserts were major contributors due to their substantial contribution and high dust concentration. Taklimakan dust, influenced by terrain and westerly winds, affected central and southern glaciers more than northern ones. Westerlies carried Thar Desert dust to the TP after it was uplifted by updrafts in northwest India, significantly affecting southern glaciers. Furthermore, comparing the two tracer methods, the indirect approach combining PSCF and CWT proved more effective for short-term dust source tracing.

The lockdowns implemented during the coronavirus disease 2019 (COVID-19) pandemic provide a unique opportunity to investigate the impact of emission sources and meteorological conditions on the trans-boundary transportation of black carbon (BC) aerosols to the Tibetan Plateau (TP). In this study, we conducted an integrative analysis, including in-situ observational data, reanalysis datasets, and numerical simulations, and found a significant reduction in the trans-boundary transport of BC to the TP during the 2020 pre-monsoon season as a result of the lockdowns and restrictive measures. Specifically, we observed a decrease of 0.0211 mu g m- 3 in surface BC concentration over the TP compared to the 2016 pre-monsoon period. Of this reduction, approximately 6.04 % can be attributed to the decrease in emissions during the COVID-19 pandemic, surpassing the 4.47 % decrease caused by changes in meteorological conditions. Additionally, the emission reductions have weakened the transboundary transport of South Asia BC to the TP by 0.0179 mu g m � 2s 1; indicating that the recurring spring atmospheric pollution from South Asia to the TP will be alleviated through the reduction of anthropogenic emissions. Moreover, it is important to note that BC deposition on glaciers contributes significantly to glacier melting due to its enrichment, posing a threat to the water sustainability of the TP. Therefore, urgent measures are needed to reduce emissions from adjacent regions to preserve the TP as the Asian Water Tower.

PM2.5 samples (n = 34) were collected from January to April 2017 over Shillong (25.7 degrees N, 91.9 degrees E; 1064 m amsl), a high-altitude site situated in the northeastern Himalaya. The main aim was to understand the sources, characteristics, and optical properties of local vs long-range transported carbonaceous aerosols (CA) using chemical species and dual carbon isotopes (13C and 14C). Percentage biomass burning (BB)/biogenic fraction (fbio, calculated from 14C) varied from 67 to 92 % (78 +/- 7) and correlated well with primary BB tracers like f60, and K+, suggesting BB as a considerable source. Rain events are shown to reduce the fbio fraction, indicating majority of BB-derived CA are transported. Further, delta 13C (-26.6 +/- 0.4) variability was very low over Shillong, suggesting it's limitations in source apportionment over the study region, if used alone. Average ratio of absorption coefficient of methanol-soluble BrC (BrCMS) to water-soluble BrC (BrCWS) at 365 nm was 1.8, indicating a significant part of BrC was water-insoluble. A good positive correlation between fbio and mass absorption efficiency of BrCWS and BrCMS at 365 nm with the higher slope for BrCMS suggests BB derived water-insoluble BrC was more absorbing. Relative radiative forcing (RRF, 300 to 2500 nm) of BrCWS and BrCMS with respect to EC were 11 +/- 5 % and 23 +/- 16 %, respectively. Further, the RRF of BrCMS was up to 60 %, and that of BrCWS was up to 22 % with respect to EC for the samples with fbio >= 0.85 (i.e., dominated by BB), reflecting the importance of BB in BrC RRF estimation.

Phosphorus (P) is an essential macronutrient for all organisms that can be redistributed between terrestrial and oceanic systems via atmospheric emission, transport, transformation, and deposition. Moreover, since natural P mobilization from the lithosphere to ecosystems is a relatively slow process, the role of atmospheric P seems to play an important role in its cycling. This paper provides a comprehensive review of the analytical methods used for characterizing atmospheric P species and the methods used for identifying P sources (e.g., oxygen stable isotope compositions of phosphate, & delta;18OP) discussing their respective suitability, advantages, and limitations. While at a regional scale & delta;18OP of atmospheric P are generally source-specific, at a more global scale these isotope compositions tend to overlap between sources, rendering their tracer potential more difficult. Further-more, various sources of atmospheric P and their fluxes are compiled, and the potential uncertainties in the estimates of their respective contributions are reviewed, which suggest that more model inter-comparations, parameter optimizations, and field observations are still needed. Moreover, we summarize the long-range transport process controlling P atmospheric dispersion at various scales (focusing on dust and biomass burning). In addition, the transformation mechanism, especially acid dissolution, that modifies the P cycle during its residence time in the atmosphere is depicted. Finally, we propose that land cover may be a potential key control to the atmospheric P deposition rate based on the critical analysis of previously published rates. This review allows us to ultimately propose key recommendations for fostering future research on P geochemical cycling.

The circum-Arctic region experienced serious fires in 2019 and 2020. Biomass burning is considered a primary source of black carbon (BC) aerosols. BC contributes to Arctic warming and impacts snow/ice melting. However, the impacts of biomass burning on BC in the Arctic during these recent serious fires have not been quantified in detail. In this study, based on numerical simulations using the Weather Research and Forecasting model coupled with Chemistry (WRF-Chem), we calculated the contribution ratios of biomass burning to Arctic BC and revealed its transport pathways. Affected by biomass burning emissions, the near-surface BC concentrations over the terrestrial areas within the Arctic Circle were highest in summer, and declined in spring and autumn. Spatially, high-concentration levels of BC were distributed in the Russian central and eastern areas. Biomass burning accounted for 63.72% and 45.18% of the summer BC in the Arctic near-surface and middle troposphere, respectively. In the near-surface, the contributions from local Arctic sources were comparable to those from sources outside the Arctic Circle in summer. In the middle troposphere, contributions from sources outside the Arctic Circle were dominant. In summer, BC originating from biomass burning in Siberia was transported a short distance by southwesterly winds to the central Arctic near-surface, while the enhanced southwesterly winds in the middle troposphere transported BC from Siberia, Alaska and northern Canada to the central Arctic and Greenland. In spring and autumn, most BC originating from biomass burning in the near-surface of Eurasia was transported eastward by westerly winds and then transported northward over the North Pacific Ocean, and the long distance may have resulted in fewer effects on the Arctic. These results highlight the important role of biomass burning in the Arctic environment under a warming climate.