This work uses a mixture of observations from surface remote sensing (AERONET) and satellite remote sensing (OMI) to uniquely compute the atmospheric column loading of black carbon (BC) mass concentration density (MCD) and number concentration density (NCD) on a grid-by-grid, day-by-day basis at 0.25 degrees x0.25 degrees over rapidly developing and biomass burning (BB) impacted regions in South, Southeast, and East Asia. This mixture of observations is uniformly analyzed based on OMI NO2 retrievals, OMI Near ultraviolet band absorption aerosol optical depth and single scattering albedo (SSA), and AERONET visible and near-infrared band SSA observations, in connection with an inversely applied MIE mixing model approach. This method uniquely solves for the unbiased spatial and temporal domains based on variance maximization of daily NO2. These locations in space and time are then used to quantify the distribution of all possible individual particle core and refractory shell sizes as constrained by all band-by-band observations of SSA from AERONET. Finally, the range of NCD and MCD are computed from the constrained range of per-particle core and refractory shell size on a grid-by-grid and day-byday basis. The maps of MCD and NCD are consistent in space and time with known urban, industrial, and BB sources. The statistical distributions are found to be non-normal, with the region-wide mean, 25th, 50th, and 75th percentile MCD [mg/m2] of 90.3, 56.1, 81.1, and 111 respectively, and NCD [x1012 particles/m2] of 8.76, 4.63, 7.39, and 11.3 respectively. On a grid-by-grid basis, a significant amount of variation is found, particularly over Myanmar, Laos, northern Thailand, and Vietnam, with this subregional mean, 25th, 50th, and 75th MCD [mg/m2] of 90.7, 56.1, 81.3, and 112 respectively and NCD [x1012 particles/m2] of 9.66, 5.49, 8.33, and 12.3 respectively. On a day-to-day basis, events are determined 121 days in 2016, during which the computed statistics of MCD and NCD have mean and uncertainty ranges which scale with each other. However, there are 11 days where the uncertainty ratio of NCD values is larger than 1 while the uncertainty ratio of MCD is small, and 5 days where the reverse is observed, indicating that the particle size is strongly atypical on these days, consistent with mixed aerosol sources, a substantial change in the aerosol aging, or other such factors including a substantial region of overlap between BB and urban sources. The high values observed from March to May lead to an extended BB season as compared to previous work focusing on fire radiative power, NO2, and models, which show a shorter season (usually ending in early April). The results are consistent with BC being able to transport significant distances. The new approach is anticipated to provide support for improving radiative forcing calculations, estimating emissions inventories, and providing a basis by which models can compare against observations.

Biomass burning play a key role in the global carbon cycle by altering the atmospheric composition, and affect regional and global climate. Despite its importance, a very few high-resolution records are available worldwide, especially for recent climate change. This study analyzes levoglucosan, a specific tracer of biomass burning emissions, in a 38-year ice core retrieved from the Shulehe Glacier No. 4, northeastern Tibetan Plateau. The levoglucosan concentration in the Shulehe Glacier No. 4 ice core ranged from 0.1 to 55 ng mL(-1), with an average concentration of 8 +/- 8 ng mL(-1). The concentrations showed a decreasing trend from 2002 to 2018. Meanwhile, regional wildfire activities in Central Asian also exhibited a declining trend during the same period, suggesting the potential correspondence between levoglucosan concentration of the Shulehe Glacier No. 4 ice core and the fire activity of Central Asia. Furthermore, a positive correlation also exists between the levoglucosan concentration of the Shulehe Glacier No. 4 ice core and the wildfire counts in Central Asia from 2002 to 2018. While backward air mass trajectory analysis and fire spots data showed a higher distribution of fire counts in South Asia compared to Central Asia, but the dominance of westerly circulation in the northern TP throughout the year. Therefore, the levoglucosan in the Shulehe Glacier No. 4 provides clear evidence of Central Asian wildfire influence on Tibetan Plateau glaciers through westerlies. This highlights a great importance of ice core data for wildfire history reconstruction in the Tibetan Plateau Glacier regions.

Freeze-thaw (FT) events profoundly perturb the biochemical processes of soil and water in mid- and high-latitude regions, especially the riparian zones that are often recognized as the hotspots of soil-water interactions and thus one of the most sensitive ecosystems to future climate change. However, it remains largely unknown how the heterogeneously composed and progressively discharged meltwater affect the biochemical cycling of the neighbor soil. In this study, stream water from a valley in the Chinese Loess Plateau was frozen at -10 degrees C for 12 hours, and the meltwater (at +10 degrees C) progressively discharged at three stages (T1 similar to T3) was respectively added to rewet the soil collected from the same stream bed (Soil+T1 similar to Soil+T3). Our results show that: (1) Approximately 65% of the total dissolved organic carbon and 53% of the total NO3--N were preferentially discharged at the first stage T1, with enrichment ratios of 1.60 similar to 1.94. (2) The dissolved organic matter discharged at T1 was noticeably more biodegradable with significantly lower SUVA(254) but higher HIX, and also predominated with humic-like, dissolved microbial metabolite-like, and fulvic acid-like components. (3) After added to the soil, the meltwater discharged at T1 (e.g., Soil+T1) significantly accelerated the mineralization of soil organic carbon with 2.4 similar to 8.07-folded k factor after fitted into the first-order kinetics equation, triggering 125 similar to 152% more total CO2 emissions. Adding T1 also promoted significantly more accumulation of soil microbial biomass carbon after 15 days of incubation, especially on the FT soil. Overall, the preferential discharge of the nutrient-enriched meltwater with more biodegradable DOM components at the initial melting stage significantly promoted the microbial growth and respiratory activities in the recipient soil, and triggered sizable CO2 emission pulses. This reveals a common but long-ignored phenomenon in cold riparian zones, where progressive freeze-thaw can partition and thus shift the DOM compositions in stream water over melting time, and in turn profoundly perturb the biochemical cycles of the neighbor soil body.

The light absorption enhancement (E-abs) of black carbon (BC) coated with non-BC materials is crucial in the assessment of radiative forcing, yet its evolution during photochemical aging of plumes from biomass burning, the globe's largest source of BC, remains poorly understood. In this study, plumes from open burning of corn straw were introduced into a smog chamber to explore the evolution of E-abs during photochemical aging. The light absorption of BC was measured with and without coating materials by using a thermodenuder, while the size distributions of aerosols and composition of BC coating materials were also monitored. E-abs was found to increase initially, and then decrease with an overall downward trend. The lensing effect dominated in E-abs at 520 nm, with an estimated contribution percentages of 47.5%-94.5%, which is far greater than light absorption of coated brown carbon (BrC). The effects of thickening and chemical composition changes of the coating materials on E-abs were evaluated through comparing measured E-abs with that calculated by the Mie theory. After OH exposure of 1 x 10(10) molecules cm(-3) s, the thickening of coating materials led to an E-abs increase by 3.2% +/- 1.6%, while the chemical composition changes or photobleaching induced an E-abs decrease by 4.7% +/- 0.6%. Simple forcing estimates indicate that coated BC aerosols exhibit warming effects that were reduced after aging. The oxidation of light-absorbing CxHy compounds, such as polycyclic aromatic hydrocarbons (PAHs), to CxHyO and CxHyO>1 compounds in coating materials may be responsible for the photobleaching of coated BrC. Plain Language Summary Understanding how black carbon (BC) coated with non-BC materials affects light absorption is crucial for assessing its impact on the Earth's climate. However, there is limited knowledge about how this process changes when BC, particularly from biomass burning, is exposed to light. Biomass burning is a significant global source of BC. This study investigated the changes in light absorption of BC from burning corn straw as it aged in a controlled environment. We measured the light absorption of BC with and without its coating materials. Our results showed that the main cause of increased light absorption was the lensing effect of the coating materials, which was more significant than the light absorption by the coating materials themselves. We also discovered that as the coating materials thickened, BC absorbed more light. However, changes in the chemical composition of the coating materials led to a decrease in total absorption. These findings suggest that while coated BC initially has a warming effect on the climate, this effect diminished as the BC ages. The decrease is likely due to the breakdown of light-absorbing compounds in the coating materials, such as polycyclic aromatic hydrocarbons (PAHs).

Carbonaceous particles are an important radiative forcing agent in the atmosphere, with large temporal and spatial variations in their concentrations and compositions, especially in remote regions. This study reported the delta C-14 and delta C-13 of total carbon (TC) and water-insoluble particulate carbon (IPC) of the total suspended particles (TSP) and PM2.5 at a remote site of the eastern Tibetan Plateau (TP), a region that is influenced by heavy air pollution from Southwest China. The average organic carbon and elemental carbon concentrations of TSP samples in this study were 3.20 +/- 2.38 mu g m(-3) and 0.68 +/- 0.67 mu g m(-3), respectively, with low and high values in summer and winter, respectively. The fossil fuel contributions of TC in TSP and PM2.5 samples were 18.91 +/- 7.22% and 23.13 +/- 12.52%, respectively, both of which were far lower than that in Southwest China, indicating the importance of non-fossil contributions from local sources. The delta C-13 of TC in TSP samples of the study site was -27.06 +/- 0.96 parts per thousand, which is between the values of long-range transported sources (e.g., Southwest China) and local biomass combustion emissions. Therefore, despite the contribution from the long-range transport of particles, aerosols emitted from local biomass combustion also have an important influence on carbonaceous particles at the study site. The findings of this work can be applied to other remote sites on the eastern TP and should be considered in related research in the future.

As an important component of organic carbon (OC), brown carbon (BrC) plays a significant role in radiative forcing in the atmosphere. Water-insoluble OC (WIOC) generally has higher light absorption ability than water-soluble OC (WSOC). The mass absorption cross- (MAC) of WIOC is normally investigated by dissolving OC in methanol. However, all the current methods have shortcomings due to neglecting the methanol insoluble particulate carbon that is detached from the filter and suspended in methanol extracts, which results in MAC uncertainties of the methanol-soluble BrC and its climate warming estimation. In this study, by investigating typical biomass combustion sourced aerosols from the Tibetan Plateau and ambient aerosols from rural and urban areas in China, we evaluated the light absorption of extractable OC fraction for the existing methods. Moreover, a new method was developed to overcome the methanol insoluble particulate carbon detachment problem to achieve more reliable MAC values. We found that OC can be dissolved in methanol in a short time (e.g., 1 h) and ultrasonic treatment and long-term soaking do not significantly increase the extractable OC fraction. Additionally, we proved that methanol insoluble particulate carbon detachment in methanol does exist in previous methods, causing overestimation of the BrC mass extracted by methanol and thus the underestimation of MAC values. We therefore recommend the newly developed extraction method in this study to be utilized in future related studies to quantitatively obtain the light absorption property of methanol-soluble BrC. (C) 2020 Elsevier Ltd. All rights reserved.

The more insects there are, the more food there is for insectivores and the higher the likelihood for insect-associated ecosystem services. Yet, we lack insights into the drivers of insect biomass over space and seasons, for both tropical and temperate zones. We used 245 Malaise traps, managed by 191 volunteers and park guards, to characterize year-round flying insect biomass in a temperate (Sweden) and a tropical (Madagascar) country. Surprisingly, we found that local insect biomass was similar across zones. In Sweden, local insect biomass increased with accumulated heat and varied across habitats, while biomass in Madagascar was unrelated to the environmental predictors measured. Drivers behind seasonality partly converged: In both countries, the seasonality of insect biomass differed between warmer and colder sites, and wetter and drier sites. In Sweden, short-term deviations from expected season-specific biomass were explained by week-to-week fluctuations in accumulated heat, rainfall and soil moisture, whereas in Madagascar, weeks with higher soil moisture had higher insect biomass. Overall, our study identifies key drivers of the seasonal distribution of flying insect biomass in a temperate and a tropical climate. This knowledge is key to understanding the spatial and seasonal availability of insects-as well as predicting future scenarios of insect biomass change.

Changing precipitation patterns and global warming have greatly changed winter snow cover, which can affect litter decomposition process by altering soil microenvironment or microbial biomass and activity. However, it remains unknown how and to what extent snow cover affects litter decomposition during winter and over longer periods of time. Here, we conducted a meta-analysis to synthesize litter decomposition studies under different levels of snow cover. Overall, deepened snow significantly enhanced litter decomposition rate and mass loss by 17% and 3%, respectively. Deepened snow enhanced litter carbon loss by 7% but did not impact the loss of litter nitrogen or phosphorus. Deepened snow increased soil temperature, decreased the frequency of freeze-thaw cycles, and stimulated microbial biomass carbon and bacterial biomass during winter, but had no effect on these parameters in summer. The promoting effect of deepened snow cover on litter decomposition in winter is mainly due to its positive effect on microbial decomposition by increasing soil temperature and reducing freezethaw cycles exceeded its negative effect on physical fragmentation of litter by reducing freeze-thaw cycles. Our findings indicate that the changes in winter snow cover under global change scenarios can greatly impact winter litter decomposition and the associated carbon cycling, which should be taken into consideration when assessing the global carbon budget in modeling.

Aerosol chemical components such as black carbon (BC) and brown carbon (BrC) regulate aerosol optical properties, which in turn drive the atmospheric radiative forcing estimations due to aerosols. In this study, we used the long-term measurements from AERONET (Aerosol Robotic Network) to better understand the aerosol types and composition with respect to their seasonal and spatial variabilities in peninsular Southeast Asia (PSEA, here defined as Vietnam, Cambodia, Thailand, Laos, and Myanmar). Two methods (i.e., aerosol type cluster and aerosol component retrieval) were applied to determine the aerosol type and chemical composition during the biomass-burning (BB) season. AERONET sites in northern PSEA showed a higher AOD (aerosol optical depth) compared to that of southern PSEA. Differences in land use pattern, geographic location, and weather regime caused much of the aerosol variability over PSEA. Lower single-scattering albedo (SSA) and higher fine-mode fraction (FMF) values were observed in February and March, suggesting the predominance of BB type aerosols with finer and stronger absorbing particles during the dry season. However, we also found that the peak BB month (i.e., March) in northern PSEA may not coincide with the lowest SSA once dust particles have mixed with the other aerosols. Furthermore, we investigated two severe BB events in March of 2014 and 2015, revealing a significant BrC fraction during BB event days. On high AOD days, although the BC fraction was high, the BrC fraction remained low due to lack of aerosol aging. This study highlights the dominance of carbonaceous aerosols in the PSEA atmosphere during the BB season, while also revealing that transported dust particles and BrC aerosol aging may introduce uncertainties into the aerosol radiative forcing calculation.

Throughcontinuous field observation and comprehensive chemicalanalysis, this study quantified the impacts of wildfire emissions,which have occurred repeatedly not only in a long-term period butalso with extensive spatial coverage, on the Himalayan ecosystem. Himalayas and Tibetan Plateau (HTP) is important forglobal biodiversityand regional sustainable development. While numerous studies haverevealed that the ecosystem in this unique and pristine region ischanging, their exact causes are still poorly understood. Here, wepresent a year-round (23 March 2017 to 19 March 2018) ground- andsatellite-based atmospheric observation at the Qomolangma monitoringstation (QOMS, 4276 m a.s.l.). Based on a comprehensive chemical andstable isotope (N-15) analysis of nitrogen compounds andsatellite observations, we provide unequivocal evidence that wildfireemissions in South Asia can come across the Himalayas and threatenthe HTP's ecosystem. Such wildfire episodes, mostly occurringin spring (March-April), not only substantially enhanced theaerosol nitrogen concentration but also altered its composition (i.e.,rendering it more bioavailable). We estimated a nitrogen depositionflux at QOMS of similar to 10 kg N ha(-1) yr(-1), which is approximately twice the lower value of the critical loadrange reported for the Alpine ecosystem. Such adverse impact is particularlyconcerning, given the anticipated increase of wildfire activitiesin the future under climate change.