Alpine grasslands are vital in regulating carbon balance on the Qinghai-Tibetan Plateau (QTP) because of the large soil organic carbon (SOC) stocks, while persistent disturbance from the endemic small semifossorial herbivore, plateau pika (Ochotona curzoniae, hereafter pika), may break this balance. Pika affect the soil microclimate by creating a heterogeneous underlying surface, which is expected to alter soil microbial communities and eventually SOC stocks. However, our knowledge regarding the potential influence mechanism is still limited. Here, we investigated vegetation biomass, soil properties and soil microbes among 4 different surfaces (i.e., original vegetation, new pika pile, old pika pile and bare patch) of typical alpine grasslands to reveal soil microbial communities and the associated effect on SOC in response to pika bioturbation. Our results showed that pika bioturbation increased both bacterial and fungal diversity and their phyla abundance for SOC decomposition. Vegetation biomass, electrical conductivity and NH4+-N accounted for the variation in both bacterial and fungal community compositions and diversity. SOC stocks were 15-30% lower in pika piles and bare patches than in the original vegetation, which was mainly attributed to the reduced soil organic matter input from vegetation and the enhanced SOC consumption by soil microbial communities. Overall, we conclude that pika bioturbation altered the diversity and composition of soil microbial communities, which was associated with SOC loss and positive carbon feedback in alpine grasslands. Our findings provide insights into the role of small semifossorial herbivores in the carbon cycle of global grasslands.

Patchiness acts as an indicator of terrestrial ecosystem degradation and can lead to considerable loss of soil organic carbon and total nitrogen. However, quantitative assessments of the effects of patchiness on soil organic carbon and total nitrogen stocks and their associated mechanisms remain limited. This study aimed to explore the influence mechanisms of patchiness on soil organic carbon and total nitrogen stocks and to project the quantitative contribution of the further expansion of patchiness and vegetation recovery. Soil properties, soil organic carbon and total nitrogen stocks were investigated using a combination of field sampling and aerial photography in four grassland types, alpine meadow, alpine steppe, temperate grassland, and desert grassland, at 47 sites in northwestern China. Soil organic carbon and total nitrogen densities in the bare patches were 34 - 54 % and 23 - 41 % lower, respectively, compared to the original vegetation. At the plot-scale, current soil organic carbon and total nitrogen stocks ranged from 30.85 to 77.80 T/ha and 3.26 to 10.19 T/ha, respectively, across grassland types; with a 10 - 27 % and 7 - 24 % potential loss of soil organic carbon and total nitrogen stocks, respectively, from the further expansion of patchiness but a 10 - 50 % and 9 - 37 % potential increase in soil organic carbon and total nitrogen stocks, respectively, from vegetation recovery. Soil organic carbon and total nitrogen stocks were positively correlated with vegetation biomass, soil clay content, and precipitation (p < 0.001), whereas they were negatively correlated with patchiness (p < 0.001). In summary, patchiness reduced soil organic carbon and total nitrogen stocks by decreasing vegetation inputs and increasing erosion outputs, while vegetation recovery showed potential for increasing carbon and nitrogen stocks. Our results highlight that maintaining intact vegetation cover is critical for preserving terrestrial ecosystem carbon and nitrogen storage.

Absorbing aerosols have significant influences on tropospheric photochemistry and regional climate change. Here, the direct radiative effects of absorbing aerosols at the major AERONET sites in East Asia and corresponding impacts on near-surface photochemical processes were quantified by employing a radiation transfer model. The average annual aerosol optical depth (AOD) of sites in China, Korea, and Japan was 1.15, 1.02 and 0.94, respectively, and the corresponding proportion of absorbing aerosol optical depth (AAOD) was 8.61%, 6.69%, and 6.49%, respectively. The influence of absorbing aerosol on ultraviolet (UV) radiation mainly focused on UV-A band (315-400 nm). Under the influence of such radiative effect, the annual mean near-surface J[NO2] (J[(OD)-D-1]) of sites in China, Korea, and Japan decreased by 16.95% (22.42%), 9.61% (13.55%), and 9.63% (13.79%), respectively. In Beijing-Tianjin-Hebei (BTH) and Yangtze River Delta (YRD) region, the annual average AOD was 1.48 and 1.29, and the AAOD was 0.14 and 0.13, respectively. The UV radiative forcing caused by aerosols dominated by black carbon (BC-dominated aerosols) on the surface was -3.19 and -2.98 W m(-2), respectively, accounting for about 40% of the total aerosol radiative forcing, indicating that the reduction efficiency of BC-dominated aerosols on solar radiation was higher than that of other types of aerosols. The annual mean J[NO2] (J[(OD)-D-1]) decreased by 14.90% (20.53%) and 13.71% (18.20%) due to the BC-dominated aerosols. The daily maximum photolysis rate usually occurred near noon due to the diurnal variation of solar zenith angle and, thus, the daily average photolysis rate decreased by 2-3% higher than that average during 10:00-14:00.

The mixing of black carbon (BC) with secondary materials is a major uncertainty source in assessing its radiative forcing. However, current understanding of the formation and evolution of various BC components is limited, particularly in the Pearl River Delta, China. This study measured submicron BC-associated nonrefractory ma-terials and the total submicron nonrefractory materials using a soot particle aerosol mass spectrometer and a high-resolution time-of-flight aerosol mass spectrometer, respectively, at a coastal site in Shenzhen, China. Two distinct atmospheric conditions were also identified to further explore the distinctive evolution of BC-associated components: polluted period (PP) and clean period (CP). Comparing the components of two particles, we found that more-oxidized organic factor (MO-OOA) prefers to form on BC during PP rather CP. The formation of MO-OOA on BC (MO-OOABC) was affected by both enhanced photochemical processes and nocturnal heterogeneous processes. Enhanced photo-reactivity of BC, photochemistry during the daytime, and heterogeneous reaction at nighttime were potential pathways for MO-OOABC formation during PP. The fresh BC surface was favorable for the formation of MO-OOABC. Our study shows the evolution of BC-associated components under different at-mospheric conditions, which should be considered in regional climate models to improve the assessment of the climate effects of BC.

Effective density (peff) is an important property describing particle transportation in the atmosphere and in the human respiratory tract. In this study, the particle size dependency of peff was determined for fresh and photochemically aged particles from residential combustion of wood logs and brown coal, as well as from an aerosol standard (CAST) burner. peff increased considerably due to photochemical aging, especially for soot agglomerates larger than 100 nm in mobility diameter. The increase depends on the presence of condensable vapors and agglomerate size and can be explained by collapsing of chain-like agglomerates and filling of their voids and formation of secondary coating. The measured and modeled particle optical properties suggest that while light absorption, scattering, and the single-scattering albedo of soot particle increase during photochemical processing, their radiative forcing remains positive until the amount of nonabsorbing coating exceeds approximately 90% of the particle mass.

The influence of the Indian summer monsoon (ISM) and mid-latitude westerlies on the central Tibetan Plateau (TP) during the Holocene, particularly during the mid-Holocene, is still unclear, limiting our understanding of past climate change in this region. Cuona Lake, located on the central TP, is a transitional zone of atmospheric circulation that is well situated for investigations on the interplay between the ISM and mid-latitude westerlies. In this study, multiple proxies of lacustrine sediments from Cuona Lake were measured, including total organic carbon (TOC), total nitrogen (TN), delta C-13(org), n-alkanes, and their hydrogen isotopes, to reconstruct the evolution of climate on the central TP over the past 13 cal kyr BP. Decreased TOC/TN ratios, dominant short-chain n-alkanes/alkanoic acid C-15/16/17, and lower values of n-alkane indicator ratios (carbon preference index and average chain length) throughout the investigated period suggest that the organic matter of the lake essentially originated from aquatic algae, and was weakly affected by terrestrial input. The historic variations in the delta D, TOC, and delta C-13(org) values revealed cold-wet conditions during 12.4-11.4 cal kyr BP, warm-wettest environments during the early Holocene (from 11.4 to 8.2 cal kyr BP), cool-wet conditions in the mid-late Holocene (from 5 to 3 cal kyr BP), and warm-dry conditions since 3 cal kyr BP. The reconstructed climatic variability in the Cuona area agrees well with previous indexes in south-central TP, indicating that the climatic pattern of the studied area is basically controlled by the monsoonal circulation from the late part of the last deglaciation to the early Holocene, with the ISM reaching the north-central TP at similar to 11 cal kyr BP. During the mid-late Holocene, the humid conditions coincided with an enhanced influence of westerlies, providing strong evidence for the contribution of westerlies-delivered moisture to the central TP. Based on a comparison of paleoclimate records, the Cuona region displays a transitional phase between monsoon circulation and westerly jets during the Holocene.

The harmonization of sampling, sample preparation and laboratory analysis methods to detect carbon compounds in snow requires detailed documentation of those methods and their uncertainties. Moreover, intercomparison experiments are needed to reveal differences and quantify the uncertainties further. Here, we document our sampling, filtering, and analysis protocols used in the intercomparison experiment from three laboratories to detect water-insoluble carbon in seasonal surface snow in the high-mountain environment at Kolm Saigurn (47.067842 degrees N, 12.98394 degrees E, alt 1598 m a.s.l.), Austria. The participating laboratories were TU Wien (Austria), the University of Florence (Italy), and the Finnish Meteorological Institute (Finland). For the carbon analysis, the NIOSH5040 and EUSAAR2 protocols of the OCEC thermal-optical method were used. The median of the measured concentrations of total carbon (TC) was 323 ppb, organic carbon (OC) 308 ppb, and elemental carbon (EC) 16 ppb. The methods and protocols used in this experiment did not reveal large differences between the laboratories, and the TC, OC, and EC values of four inter-comparison locations, five meters apart, did not show meter-scale horizontal variability in surface snow. The results suggest that the presented methods are applicable for future research and monitoring of carbonaceous particles in snow. Moreover, a recommendation on the key parameters that an intercomparison experiment participant should be asked for is presented to help future investigations on carbonaceous particles in snow. The work contributes to the harmonization of the methods for measuring the snow chemistry of seasonal snow deposited on the ground.

Climate change is destabilizing permafrost landscapes, affecting infrastructure, ecosystems, and human livelihoods. The rate of permafrost thaw is controlled by surface and subsurface properties and processes, all of which are potentially linked with each other. However, no standardized protocol exists for measuring permafrost thaw and related processes and properties in a linked manner. The permafrost thaw action group of the Terrestrial Multidisciplinary distributed Observatories for the Study of the Arctic Connections (T-MOSAiC) project has developed a protocol, for use by non-specialist scientists and technicians, citizen scientists, and indigenous groups, to collect standardized metadata and data on permafrost thaw. The protocol introduced here addresses the need to jointly measure permafrost thaw and the associated surface and subsurface environmental conditions. The parameters measured along transects include: snow depth, thaw depth, vegetation height, soil texture, and water level. The metadata collection includes data on timing of data collection, geographical coordinates, land surface characteristics (vegetation, ground surface, water conditions), as well as photographs. Our hope is that this openly available dataset will also be highly valuable for validation and parameterization of numerical and conceptual models, and thus to the broad community represented by the T-MOSAiC project.

Though one of the most vulnerable terrestrial ecosystems, wetlands provide multiple ecosystem services, most notably storing carbon. It is now widely recognized that climate change could have a large impact on high-latitude wetlands. A key question is how climate change will affect the distribution pattern of wetland plant communities, and to what extent the transitions among different wetland plant communities respond to regional warming? To answer this question, we estimated the total SOC storage with 139 soil profiles in the Xing'anling Mountains and performed ensemble species distribution modelling for 11 dominant wetland plant communities by using numerous vegetation plots. Results show that 4.5-23.8% of the high-latitude wetlands in the study area would be lost following widespread thawing of permafrost under different climate warming scenarios by the end of this century. The total wetland SOC in the Xing'anling Mountains is estimated to be 1.58 Pg, about 25.5-29.3% of the total of China's wetlands, however, predicted wetland loss could put 5.4-20.5% (0.08-0.32 Pg C) of the total SOC storage at risk of instability. Our results also predicted a significant northward migration of southern Deyeuxia angustifolia communities driven by future climate changes. This wetland succession could profoundly reduce future carbon sequestration capacity of wetlands in the study area. The findings presented here are helpful for both current reserve management and future conservation planning of wetlands in the study area.

Atmospheric particle is one of the major air pollutants, and believed to be important for air quality, radiative forcing and climate. Measurements of aerosol optical properties, size distribution and PM10 concentration were conducted at Orleans, central France during spring (7 March to 25 April) and autumn (25 October to 5 December) 2013. The average values of aerosol scattering coefficient (b(sca)), absorption coefficient (b(abs)), single scattering albedo (SSA) at 532 nm and PM10 concentration are 54.9 +/- 58.2 Mm(-1), 10.6 +/- 10.9 Mm(-1), 0.81 +/- 0.10 and 30.6 +/- 21.6 mu g/m(3) for the spring campaign, and 35.4 +/- 36.7 Mm(-1), 3.9 +/- 4.4 Mm(-1), 0.83 +/- 0.13 and 17.4 +/- 11.8 mu g/m(3) for the autumn campaign, respectively. During the whole observation, the air parcel transported from Atlantic Ocean plays a role in cleaning up the ambient air in Orleans, while the air mass coining from the Eastern Europe induces the pollution events in Orleans. In this study, a simple approach, which based on the diurnal variation of PM10 concentration, Boundary layer depth (BLD) and the human activity factor derived from anthropogenic emission rate, was introduced to estimate the contribution of secondary aerosol to ambient aerosols. Our results show that secondary particles formation trigged by photochemical reactions and oxidations can contribute maximum of 64% and 32% for PM10 mass concentration during the spring and autumn time, respectively. These results highlight that photochemical reactions can enhance the atmospheric oxidation capacity and may faster the secondary particle formation and then play an important role in air quality. (C) 2018 Elsevier B.V. All rights reserved.