Elemental carbon (EC), also known as black carbon, plays an important role in climate change. Accurately assessing EC concentration in aerosols remains challenging due to the overestimations caused by carbonates and organic carbon (OC) during thermal-optical measurement in the Tibetan Plateau (TP). This study evaluates the extent of EC overestimated by carbonates and OC at four remote sites (Nyalamu, Lulang, Everest and Ngari) in southern and western of the TP using different treatments. The average overestimation of EC concentration due to acid treatment was consistent across all sites (25.5 f 2.4 %). After correction, the proportion of EC overestimated by carbonates were approximately 8.5 f 7.3 %, 12.3 f 6.9 %, 18.1 f 11.8 % and 22.7 f 13.3 %, respectively, revealing an increasing trend from humid to arid regions. Methanol-soluble OC (MSOC) concentrations were significantly correlated with the reduction of EC concentrations, indicating that the methanol extraction effectively mitigates EC overestimation. Seasonal variation of carbonaceous aerosol concentrations was significantly affected by sources from South Asia. Despite the variations in climate and aerosol sources, the average overestimations of measured EC concentration by carbonates and OC were similar at Nyalamu (49.4 f 14.0 %), Lulang (47.8 f 8.4 %), Everest (48.7 f 15.9 %) and Ngari (49.3 f 13.7 %) sites. Therefore, the actual EC concentrations were only about 51.2 f 13.1 % of the original values. This estimation will significantly enhance the contribution of brown carbon (BrC) to radiative forcing relative to EC, highlighting a critical area for future research. Investigating the actual concentrations of EC in the TP provides critical data to support model simulation and validate model accuracy, further enhancing our understanding of EC's impacts on climate warming and glacier melting.

Carbonaceous particles have been confirmed as major components of ambient aerosols in urban environments and are related to climate impacts and environmental and health effects. In this study, we collected different-size particulate matter (PM) samples (PM1, PM2.5, and PM10) at an urban site in Lanzhou, northwest China, during three discontinuous one-month periods (January, April, and July) of 2019. We measured the concentrations and potential transport pathways of carbonaceous aerosols in PM1, PM2.5, and PM10 size fractions. The average concentrations of OC (organic carbon) and EC (elemental carbon) in PM1, PM2.5, and PM10 were 6.98 +/- 3.71 and 2.11 +/- 1.34 mu g/m(3), 8.6 +/- 5.09 and 2.55 +/- 1.44 mu g/m(3), and 11.6 +/- 5.72 and 4.01 +/- 1.72 mu g/m(3). The OC and EC concentrations in PM1, PM2.5, and PM10 had similar seasonal trends, with higher values in winter due to the favorable meteorology for accumulating pollutants and urban-increased emissions from heating. Precipitation played a key role in scavenge pollutants, resulting in lower OC and EC concentrations in summer. The OC/EC ratios and principal component analysis (PCA) showed that the dominant pollution sources of carbon components in the PMs in Lanzhou were biomass burning, coal combustion, and diesel and gasoline vehicle emissions; and the backward trajectory and concentration weight trajectory (CWT) analysis further suggested that the primary pollution source of EC in Lanzhou was local fossil fuel combustion.

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 of the Yellow River between its source and Hekou Town in Inner Mongolia is known as the Upper Yellow River Basin. It is the main source area of water resources in the Yellow River Basin, providing reliable water resources for 120 million people. Studying the hydrometeorological changes in the Upper Yellow River Basin is crucial for the development of human society. However, in the past, there has been limited research on hydrometeorological changes in the Upper Yellow River Basin. In order to clarify the four-dimensional spatiotemporal variation characteristics of hydrometeorological elements in the Upper Yellow River Basin, satellite and reanalysis hydrometeorological elements products need to be used. Unfortunately, there is currently a lack of precise evaluation studies on satellite and reanalysis hydrometeorological elements products in the Upper Yellow River Basin, and the geomorphic characteristics of this area have raised doubts about the accuracy of satellite and reanalysis hydrometeorological elements products. Thus, the evaluation study in the Upper Yellow River Basin is an important prerequisite for studying the four-dimensional spatiotemporal changes of hydrometeorological elements. When conducting evaluation study, we found that previous evaluation studies had a very confusing understanding of the spatiotemporal characteristics of datasets. Some papers even treated the spatiotemporal characteristics of evaluation metrics as the spatiotemporal characteristics of datasets. Therefore, we introduced a four-dimensional spacetime of both datasets and evaluation metrics to rectify the chaotic spatiotemporal view in the past. Our research results show that satellite and reanalysis hydrometeorological elements products have different abilities in describing the temporal and spatial distribution and change characteristics of hydrometeorological elements. The difference in the ability of satellite and reanalysis hydrometeorological elements products to describe temporal and spatial distribution and change characteristics requires us to select data at different temporal and spatial scales according to research needs when conducting hydrometeorological research, in order to ensure the credibility of the research results.

Progressive climate change may have unpredictable consequences for the Arctic environment. Permafrost catchments off the west coast of Svalbard, described as thin and warm, are particularly sensitive to climate change. The interdisciplinary research on the hydrochemical response of surface and underground water functioning within a small permafrost catchment area focused on the determination of the impact of meteorological conditions (temperature (T), precipitation (P)) on the mean daily discharge (Q), and the lowering of the groundwater table (H). We determined physical and chemical properties (pH and SEC) and concentrations of major elements (Ca, Mg, Na, K) and 23 trace elements (i.a. Cd, Cu, Hg, Pb, Zn) in 280 water samples. The results of the correlation matrix showed that an increase in the average air temperature in the summer of 2021 had a significant impact on the hydrochemistry of both types of waters operating in the catchment. In response to increase in T, the lowering of the H (0.52 < r < 0.66) and a decrease in Q (-0.66 < r < -0.68) were observed what in consequence also leads to changes in water chemistry. The principal component analysis (CA) indicates that chemical weathering and binding of elements to DOC are processes influencing water chemistry. Results of statistical analysis showed that the resultant of the hydrometeorological conditions that prevailed in that season and the type of geological formations on which they were located had a significant impact on the water chemistry at individual measurement points. Significant differences in the concentrations of elements between points on the same geological formations were also found.

There is an increased awareness that the biogeochemical cycling at high latitudes will be affected by a changing climate. However, because biogeochemical studies most often focus on a limited number of elements (i.e., C, P and N) we lack baseline conditions for many elements. In this work, we present a 42-element mass-balance budget for lake dominated catchment in West Greenland. By combining site specific concentration data from various catchment compartments (precipitation, active layer soils, groundwater, permafrost, lake water, lake sediments and biota) with catchment geometries and hydrological fluxes from a distributed hydrological model we have assessed present-day mobilization, transport and accumulation of a whole suite of elements with different biogeochemical behavior. Our study shows that, under the cold and dry conditions that prevails close to the inland ice-sheet: i) eolian processes are important for the transport of elements associated with mineral particles (e.g., Al, Ti, Si), and that these elements tend to accumulate in the lake sediment, ii) that even if weathering rates are slowed down by the dry and cold climate, weathering in terrestrial soils is an important source for many elements (e.g., lanthanides), iii) that the cold and dry conditions results in an accumulation of elements supplied by wet deposition (e.g., halogens) in both terrestrial soils and the lake-water column, and iv) that lead and sulfur from legacy pollution are currently being released from the terrestrial system. All these processes are affected by the climate, and we can therefore expect that the cycling of the majority of the 42 studied elements will change in the future. However, it is not always possible to predict the direction of this change, which shows that more multi-element biogeochemical studies are needed to increase our understanding of the consequences of a changing climate for the Arctic environment.

Trace elements (TEs) in water are crucial parameters for assessing water quality. However, detailed studies are limited on TEs in the hydrological system of the Tibetan plateau (TP). Here, we sampled snow, river water, and groundwater in Yulong Snow Mountain (Mt. Yulong) region, southeast TP, in 2016 and analyzed the concentrations of nine TEs (namely Al, Mn, Fe, Cr, Ni, Cu, Zn, As, and Pb). In snow, the average concentrations of Fe, Zn, and Al were >10 mu g/L, whereas other elements, including Cr, Ni, Cu, As, Hg, and Pb, exhibited average concentrations <1 mu g/L. The concentrations of Al, Mn, Fe, Zn, and As were higher in rivers than in snow. According to enrichment factors (EFs), Zn concentration in snow was highly influenced by anthropogenic activities, whereas Mn, Fe, Cr, and As were uninfluenced. River and lake/reservoir water near human settlements were affected by anthropogenic activities. However, groundwater around Mt. Yulong is not contaminated yet. The increasing EFs in Mt. Yulong snowpit are consistent with those of southern TP snowpits, suggesting that the area has been affected by anthropogenic activities both from local emissions and long-distance transport of pollutants from South Asia. A conceptual model was proposed to show TEs in the water cycle. Although water quality is good overall in Mt. Yulong region, threats to the water environment still exit due to increasing anthropogenic activities and climate warming. The accelerated ablation of cryosphere due to climate warming could be a source of TEs in rivers and groundwater, which should be paid attention to in the future. (C) 2020 Elsevier B.V. All rights reserved.

Glacial sediments as an important end member of the global dust system, could indicate changes in global climate, aerosols sources, ocean elements, and productivity. With global warming, ice caps shrinking and glaciers retreat at high latitudes have attracted concern. To understand the response of glacier to environment and climate in modern high latitude ice-marginal environments, this paper investigated glacial sediments in the Ny-angstrom lesund region of the Arctic and clarified the response of polar environmental to global changes through geochemical characteristics of glacial sediments. The results showed that: 1) main factors affecting the elements distribution of the Ny-angstrom lesund glacial sediments were thought as soil formation, bedrock and weathering, and biological activity; 2) variations of SiO2/Al2O3 and SiO2/Al2O3 + Fe2O3, indicating low weathering of the soil. The ratio of Na2O/K2O indicating a weak chemical weathering, was negatively correlated to the CIA. With the average CIA of Ny-angstrom lesund glacial sediments for main minerals of quartz, feldspar, and muscovite as well as dolomite and calcite 50.13, which implied glacial sediments at the early stage of chemical weathering and depletion of Ca and Na; 3) the separating effect of stones and soils by stone circle formation due to thermal conductivity and frost heave makes sediments in stone circle have lower chemical weathering with only two main minerals, albite and quartz; 4) changes of carbonate content in sediments with glacier front retreating in different period implied that weathering rate of calcite averagely reached an estimate of 0.0792% wt/year in glacier A. The succession of vegetation made biological weathering become an important driving force for carbonate leaching from glacial sediments. These results and data provide scientifically significant archive for future global change studies.

Particulate black carbon (BC) affects global warming by absorbing the solar radiation, by affecting cloud formation, and by decreasing ground albedo when deposited to snow or ice. BC has also a wide variety of adverse effects on human population health. In this article we reviewed the BC emission factors (EFs) of major anthropogenic sources, i.e. traffic (incl. marine and aviation), residential combustion, and energy production. We included BC EFs measured directly from individual sources and EFs derived from ambient measurements. Each source category was divided into sub-categories to find and demonstrate systematical trends, such as the potential influence of fuel, combustion technologies, and exhaust/flue gas cleaning systems on BC EFs. Our review highlights the importance of society level emission regulation in BC emission mitigation; a clear BC emission reduction was observed in ambient studies for road traffic as well as in direct emission measurements of diesel-powered individual vehicles. However, the BC emissions of gasoline vehicles were observed to be higher for vehicles with direct fuel injection techniques (gasoline direct injection) than for vehicles with port-fueled injection, indicating potentially negative trend in gasoline vehicle fleet BC EFs. In the case of shipping, a relatively clear correlation was seen between the engine size and BC EFs so that the fuel specific BC EFs of the largest engines were the lowest. Regarding the BC EFs from residential combustion, we observed large variation in EFs, indicating that fuel type and quality as well as combustion appliances significantly influence BC EFs. The largest data gaps were in EFs of large-scale energy production which can be seen crucial for estimating global radiative forcing potential of anthropogenic BC emissions. In addition, much more research is needed to improve global coverage of BC EFs. Furthermore, the use of existing data is complicated by different EF calculation methods, different units used in reporting and by variation of results due to different experimental setups and BC measurement methods. In general, the conducted review of BC EFs is seen to significantly improve the accuracy of future emission inventories and the evaluations of the climate, air quality, and health impacts of anthropogenic BC emissions.

Characteristics of carbonaceous aerosol (CA) and its light absorption properties are limited in Karachi, which is one of the most polluted metropolitan cities in South Asia. This study presents a comprehensive measurement of seasonality of CA compositions and mass absorption cross- (MAC) of elemental carbon (EC) and water-soluble organic carbon (WSOC) in total suspended particles (TSP) collected from February 2015 to March 2017 in the southwest part of Karachi. The average TSP, organic carbon (OC), and EC concentrations were extremely high with values as 391.0 +/- 217.0, 37.2 +/- 28.0, and 8.53 +/- 6.97 mg/m(3), respectively. These components showed clear seasonal variations with high concentrations occurring during fall and winter followed by spring and summer. SO42-, NO3-, K+, and NH4+ showed similar variations with CA, implying the significant influence on atmospheric pollutants from anthropogenic activities. Relatively lower OC/EC ratio (4.20 +/- 2.50) compared with remote regions further indicates fossil fuel combustion as a primary source of CA. Meanwhile, sea salt and soil dust are important contribution sources for TSP. The average MAC of EC (632 nm) and WSOC (365 nm) were 6.56 +/- 2.70 and 0.97 +/- 0.37 m(2)/g, respectively. MACEC is comparable to that in urban areas but lower than that in remote regions, indicating the significant influence of local emissions. MACWSOC showed opposite distribution with EC, further suggesting that OC was significantly affected by local fossil fuel combustion. In addition, dust might be an important factor increasing MACWSOC particularly during spring and summer. (C) 2020 The Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences. Published by Elsevier B.V.