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.

Microplastics have recently been detected in the atmosphere of urban, suburban, and even remote areas far away from source regions of microplastics, suggesting the potential long-distance atmospheric transport for microplastics. There still exist questions regarding the occurrence, fate, transport, and effect of atmospheric microplastics. These questions arise due to limited physical analysis and understanding of atmospheric microplastic pollution in conjunction with a lack of standardized sampling and identification methods. This paper reviews the current status of knowledge on atmospheric microplastics, the methods for sample collection, analysis and detection. We review and compare the methods used in the previous studies and provide recommendations for atmospheric microplastic sampling and measurement. Furthermore, we summarize the findings related to atmospheric microplastic characteristics, including abundance, size, shapes, colours, and polymer types. Microplastics occur in the atmosphere from urban to remote areas, with an abundance/deposition spanning 1-3 orders of magnitude across different sites. Fibres and fragments are the most frequently reported shapes and the types of plastic which generally aligns with world plastic demand. We conclude that atmospheric microplastics require further research and greater understanding to identify its global distributions and potential exposure to human health through further field sampling and implementation of standardized analytical protocols.

This paper provides an overview and summary of the current state of knowledge regarding critical atmospheric processes that affect the distribution and concentrations of greenhouse gases and aerosols emitted from wildland fires or produced through subsequent chemical reactions in the atmosphere. These critical atmospheric processes include the dynamics of plume rise, chemical reactions involving smoke plume constituents, the long-range transport of smoke plumes, and the potential transport of gases and aerosols from wildland fires into the stratosphere. In the area of plume-rise dynamics, synthesis information is provided on (I) the relevance of plume height for assessing impacts of gases and aerosol from wildland fires on the climate system, (2) recent scientific advances in understanding the role of multiple updraft cores in plume behavior, and (3) some of the current modeling tools and remote sensing monitoring techniques available for predicting and measuring smoke plume heights. In the area of atmospheric chemistry associated with wildland fire emissions, synthesis information is provided on what is currently known about the atmospheric fate of wildland fire smoke-plume constituents and the relationship of their atmospheric chemistry to radiative forcing. Synthesis information related to long-range atmospheric transport of wildland fire emissions is presented and summarizes many of the recent published observational and modeling studies that provide clear evidence of intercontinental, continental, and regional transport of North American fire emissions, including black carbon, to locations far-removed from the fire-event locations. Recent studies are also highlighted that examined the significance of troposphere-stratosphere exchange processes, which can result in the transport of greenhouse gases and aerosols from North American wildland fires into the stratosphere where they can remain for very long periods of time and alter the radiative balance and typical chemical reactions that occur there. Finally, specific research gaps and needs related to plume dynamics, atmospheric transport and deposition processes, and the atmospheric chemistry of wildland fire emissions are identified and discussed. Published by Elsevier B.V.