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A monitoring programme for halogenated climate-altering gases has been established in the frame of the SHARE EV-K2-CNR project at the Nepal Climate Laboratory - Pyramid in the Himalayan range at the altitude of 5079ma.s.I. The site is very well located to provide important insights on changes in atmospheric composition in a region that is of great significance for emissions of both anthropogenic and biogenic halogenated compounds. Measurements are performed since March 2006, with grab samples collected on a weekly basis. The first three years of data have been analysed. After the identification of the atmospheric background values for fourteen halocarbons, the frequency of occurrence of pollution events have been compared with the same kind of analysis for data collected at other global background stations. The analysis showed the fully halogenated species, whose production and consumption are regulated under the Montreal Protocol, show a significant occurrence of "'above the baseline" values, as a consequence of their current use in the developing countries surrounding the region, meanwhile the hydrogenated gases, more recently introduced into the market, show less frequent spikes. Atmospheric concentration trends have been calculated as well, and they showed a fast increase, ranging from 5.7 to 12.6%, of all the hydrogenated species, and a clear decrease of methyl chloroform (-17.7%). The comparison with time series from other stations has also allowed to derive Meridional gradients, which are absent for long living well mixed species, while for the more reactive species, the gradient increases inversely with respect to their atmospheric lifetime. The effect of long range transport and of local events on the atmospheric composition at the station has been analysed as well, allowing the identification of relevant source regions the Northern half of the Indian sub-continent. Also, at liner spatial scales, a smaller, local contribution of forest fires from the Khumbu valley has been detected. [ABSTRACT FROM AUTHOR]

Aerosol mass and the absorbing fraction are important variables, needed to constrain the role of atmospheric particles in the Earth radiation budget, both directly and indirectly through CCN activation. In particular, their monitoring in remote areas and mountain sites is essential for determining source regions, elucidating the mechanisms of long range transport of anthropogenic pollutants, and validating regional and global models. Since March 2006, aerosol mass and black carbon concentration have been monitored at the Nepal Climate Observatory-Pyramid, a permanent high-altitude research station located in the Khumbu valley at 5079 m a.s.l. below Mt. Everest. The first twoyear averages of PM1 and PM1-10 mass were 1.94 μgm-3 and 1.88 μgm-3, with standard deviations of 3.90 μgm-3 and 4.45 μgm-3, respectively, while the black carbon concentration average is 160.5 ng m-3, with a standard deviation of 296.1 ng m-3. Both aerosol mass and black carbon show well defined annual cycles, with a maximum during the premonsoon season and a minimum during the monsoon. They also display a typical diurnal cycle during all the seasons, with the lowest particle concentration recorded during the night, and a considerable increase during the afternoon, revealing the major role played by thermal winds in influencing the behaviour of atmospheric compounds over the high Himalayas. The aerosol concentration is subject to high variability: in fact, as well as frequent "background conditions" (55% of the time) when BC concentrations are mainly below 100 ngm-3, concentrations up to 5 μgm-3 are reached during some episodes (a few days every year) in the premonsoon seasons. The variability of PM and BC is the result of both short-term changes due to thermal wind development in the valley, and long-range transport/synoptic circulation. At NCO-P, higher concentrations of PM1 and BC are mostly associated with regional circulation and westerly air masses from the Middle East, while the strongest contributions of mineral dust arrive from the Middle East and regional circulation, with a special contribution from North Africa and South-West Arabian Peninsula in post-monsoon and winter season. [ABSTRACT FROM AUTHOR]

We report chemical composition data for PM10 and PM1 from the Nepal Climate Observatory-Pyramid (NCO-P), the world's highest aerosol observatory, located at 5079m a.s.l. at the foothills of Mt. Everest. Despite its high altitude, the average PM10 mass apportioned by the chemical analyses is of the order of 6 μgm-3 (i.e., 10 μg/scm), with almost a half of this mass accounted for by organic matter, elemental carbon (EC) and inorganic ions, the rest being mineral dust. Organic matter, in particular, accounted for by 2.0 μgm-3 (i.e., 3.6 μg/scm) on a yearly basis, and it is by far the major PM10 component beside mineral oxides. Non-negligible concentrations of EC were also observed (0.36 μg/scm), confirming that light-absorbing aerosol produced from combustion sources can be efficiently transported up the altitudes of Himalayan glaciers. The concentrations of carbonaceous and ionic aerosols follow a common time trend with a maximum in the premonsoon season, a minimum during the monsoon and a slow recovery during the postmonsoon and dry seasons, which is the same phenomenology observed for other Nepalese Himalayan sites in previous studies. Such seasonal cycle can be explained by the seasonal variations of dry and moist convection and of wet scavenging processes characterizing the climate of north Indian subcontinent. We document the effect of orographic transport of carbonaceous and sulphate particles upslope the Himalayas, showing that the valley breeze circulation, which is almost permanently active during the out-of-monsoon season, greatly impacts the chemical composition of PM10 and PM1 in the high Himalayas and provides an efficient mechanism for bringing anthropogenic aerosols into the Asian upper troposphere (>5000m a.s.l.). The concentrations of mineral dust are impacted to a smaller extent by valley breezes and follow a unique seasonal cycle which suggest multiple source areas in central and south-west Asia. Our findings, based on two years of observations of the aerosol chemical composition, provide clear evidence that the southern side of the high Himalayas is impacted by transport of anthropogenic aerosols which constitute the Asian brown cloud. [ABSTRACT FROM AUTHOR]

In this work, we present the first systematic identification of episodes of air mass transport from the lower stratosphere/upper troposphere (LS/UT) in the middle troposphere of the southern Himalayas. For this purpose, we developed an algorithm to detect LS/UT transport events on a daily basis at the Everest-Pyramid GAW station (EV-PYR, 5079 m a.s.l., Nepal). In particular, in situ surface ozone and atmospheric pressure variations as well as total ozone values from OMI satellite measurements have been analysed. Further insight is gained from three-dimensional backward trajectories and potential vorticity calculated with the LAGRANTO model. According to the algorithm outputs, 9.0% of the considered data set (365 days from March 2006 to February 2007) was influenced by this class of phenomena with a maximum of frequency during dry and pre-monsoon seasons. During 25 days of LS/UT transport events for which any influence of anthropogenic pollution was excluded, the daily ozone mixing ratio increased by 9.3% compared to the seasonal values. This indicates that under favourable conditions, downward air mass transport from the LS/UT can play a considerable role in determining the concentrations of surface ozone in the southern Himalayas. [ABSTRACT FROM AUTHOR]

To study the influence of polluted air-mass transport carrying ozone (O 3 ) and black carbon (BC) in the high Himalayas, since March 2006 the Nepal Climate Observatory at Pyramid (NCO-P) GAW-WMO global station (Nepal, 5079 m a.s.l.) is operative. During the first 5-year measurements, the O 3 and BC concentrations have shown a mean value of 48 ± 12 ppb (± standard deviation) and 208 ± 374 ng/m 3 , respectively. Both O 3 and BC showed well defined seasonal cycles with maxima during pre-monsoon (O 3 : 61.3 ± 7.7 ppbV; BC: 444 ± 433 ng/m 3 ) and minima during the summer monsoon (O 3 : 40.1 ± 12.4 ppbV; BC: 64 ± 101 ng/m 3 ). The analysis of the days characterised by the presence of a significant BC increase with respect to the typical seasonal cycle identified 156 days affected by “acute” pollution events, corresponding to 9.1% of the entire data-set. Such events mostly occur in the pre-monsoon period, when the O 3 diurnal variability is strongly related to the transport of polluted air-mass rich on BC. On average, these “acute” pollution events were characterised by dramatic increases of BC (352%) and O 3 (29%) levels compared with the remaining days. [ABSTRACT FROM AUTHOR]