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      Mixing state and hygroscopicity of dust and haze particles before leaving Asian continent : INDIVIDUAL PARTICLES IN ASIAN OUTFLOW

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          Aerosols, climate, and the hydrological cycle.

          Human activities are releasing tiny particles (aerosols) into the atmosphere. These human-made aerosols enhance scattering and absorption of solar radiation. They also produce brighter clouds that are less efficient at releasing precipitation. These in turn lead to large reductions in the amount of solar irradiance reaching Earth's surface, a corresponding increase in solar heating of the atmosphere, changes in the atmospheric temperature structure, suppression of rainfall, and less efficient removal of pollutants. These aerosol effects can lead to a weaker hydrological cycle, which connects directly to availability and quality of fresh water, a major environmental issue of the 21st century.
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            Direct observations of atmospheric aerosol nucleation.

            Atmospheric nucleation is the dominant source of aerosol particles in the global atmosphere and an important player in aerosol climatic effects. The key steps of this process occur in the sub-2-nanometer (nm) size range, in which direct size-segregated observations have not been possible until very recently. Here, we present detailed observations of atmospheric nanoparticles and clusters down to 1-nm mobility diameter. We identified three separate size regimes below 2-nm diameter that build up a physically, chemically, and dynamically consistent framework on atmospheric nucleation--more specifically, aerosol formation via neutral pathways. Our findings emphasize the important role of organic compounds in atmospheric aerosol formation, subsequent aerosol growth, radiative forcing and associated feedbacks between biogenic emissions, clouds, and climate.
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              Long-range atmospheric transport of soil dust from Asia to the tropical north pacific: temporal variability.

              The concentration of airborne soil dust at Enewetak Atoll(11 degrees N, 162 degrees E) in April 1979 was 2.3 micrograms per cubic meter but decreased steadily to 0.02 microgram per cubic meter over the next 5 months. The spring dust is probably derived from China; its deposition rate ( approximately 0.3 millimeter per 1000 years) suggests that it may be a significant contributor to the deep-sea sediments of the North Pacific.
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                Author and article information

                Journal
                Journal of Geophysical Research: Atmospheres
                J. Geophys. Res. Atmos.
                Wiley
                2169897X
                January 27 2014
                January 27 2014
                January 17 2014
                : 119
                : 2
                : 1044-1059
                Affiliations
                [1 ]Environment Research Institute; Shandong University; Jinan China
                [2 ]State Key Laboratory of Coal Resources and Safe Mining; China University of Mining and Technology; Beijing China
                [3 ]School of Geography, Earth and Environmental Sciences; University of Birmingham; Birmingham UK
                [4 ]Key Laboratory of Atmospheric Chemistry; Chinese Academy of Meteorological Sciences; Beijing China
                [5 ]State Key Laboratory of Atmospheric Boundary Layer Physics and Atmospheric Chemistry, Institute of Atmospheric Physics; Chinese Academy of Sciences; Beijing China
                Article
                10.1002/2013JD021003
                3f5411c0-7efd-4bcf-b2ec-458a2441a51e
                © 2014

                http://doi.wiley.com/10.1002/tdm_license_1.1

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