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The Kathmandu Valley in south Asia is considered as one of the global "hot spots" in terms of urban air pollution. It is facing severe air quality problems as a result of rapid urbanization and land use change, socioeconomic transformation, and high population growth. In this paper, we present the first full year (February 2013-January 2014) analysis of simultaneous measurements of two shortlived climate forcers/pollutants (SLCF/P), i.e., ozone (O3) and equivalent black carbon (hereinafter noted as BC) and aerosol number concentration at Paknajol, in the city center of Kathmandu. The diurnal behavior of equivalent BC and aerosol number concentration indicated that local pollution sources represent the major contributions to air pollution in this city. In addition to photochemistry, the planetary boundary layer (PBL) and wind play important roles in determining O3 variability, as suggested by the analysis of seasonal changes of the diurnal cycles and the correlation with meteorological parameters and aerosol properties. Especially during pre-monsoon, high values of O3 were found during the afternoon/evening. This could be related to mixing and entrainment processes between upper residual layers and the PBL. The high O3 concentrations, in particular during pre-monsoon, appeared well related to the impact of major open vegetation fires occurring at the regional scale. On a synoptic-scale perspective, westerly and regional atmospheric circulations appeared to be especially conducive for the occurrence of the high BC and O3 values. The very high values of SLCF/P, detected during the whole measurement period, indicated persisting adverse air quality conditions, dangerous for the health of over 3 million residents of the Kathmandu Valley, and the environment. Consequently, all of this information may be useful for implementing control measures to mitigate the occurrence of acute pollution levels in the Kathmandu Valley and surrounding area. [ABSTRACT FROM AUTHOR]

The Kathmandu Valley in South Asia is considered as one of the global "hot spots" in terms of urban air pollution. It is facing severe air quality problems as a result of rapid urbanization and land use change, socioeconomic transformation and high population growth. In this paper, we present the first full year (February 2013-January 2014) analysis of simultaneous measurements of two short-lived climate forcers/pollutants (SLCF/P), i.e. ozone (O3) and equivalent black carbon (hereinafter noted as BC) and aerosol number concentration at Paknajol, in the center of the Kathmandu metropolitan city. The diurnal behavior of equivalent black carbon (BC) and aerosol number concentration indicated that local pollution sources represent the major contributions to air pollution in this city. In addition to photochemistry, the planetary boundary layer (PBL) and wind play important roles in determining O3 variability, as suggested by the analysis of seasonal diurnal cycle and correlation with meteorological parameters and aerosol properties. Especially during pre-monsoon, high values of O3 were found during the afternoon/evening; this could be related to mixing and entrainment processes between upper residual layers and the PBL. The high O3 concentrations, in particular during premonsoon, appeared well related to the impact of major open vegetation fires occurring at regional scale. On a synoptic-scale perspective, westerly and regional atmospheric circulations appeared to be especially conducive for the occurrence of the high BC and O3 values. The very high values of SLCF/P, detected during the whole measurement period, indicated persisting adverse air quality conditions, dangerous for the health of over 3 million residents of the Kathmandu Valley, and the environment. Consequently, all of this information may be useful for implementing control measures to mitigate the occurrence of acute pollution levels in the Kathmandu Valley and surrounding area. [ABSTRACT FROM AUTHOR]

This work investigates the variability of ozone (O3), carbon monoxide (CO) and equivalent black carbon (BC) at the Italian Climate Observatory "O. Vittori" (ICO- OV), part of the Mt. Cimone global GAW-WMO station (Italy). For this purpose, ICO-OV observations carried out in the period January 2007-June 2009, have been analyzed and correlated with the outputs of the FLEXPART Lagrangian dispersion model to specifically evaluate the influence of biomass burning (BB) and anthropogenic emissions younger than 20 days. During the investigation period, the average O3, CO and BC at ICO-OV were 54±3ppb, 122±7ppb and 213±34 ng m-3 (mean±expanded uncertainty with p < 95 %), with clear seasonal cycles characterized by summer maxima and winter minima for O3 and BC and spring maximum and summer minimum for CO. According to FLEXPART outputs, BB impact is maximized during the warm months from July to September but appeared to have a significant contribution to the observed tracers only during specific transport events. We characterised in detail five "representative" events with respect to transport scales (i.e. global, regional and local), source regions and O3, CO and BC variations. For these events, very large variability of enhancement ratios O3/CO (from -0.22 to 0.71) and BC/CO (from 2.69 to 29.83 ng m-3 ppb-1) were observed. CO contributions related with anthropogenic emissions (COant) contributed to 17.4 % of the mean CO value observed at ICO-OV, with the warm months appearing particularly affected by transport events of air-masses rich in anthropogenic pollution. The proportion of tracer variability that is described by FLEXPART COant peaked to 37% (in May-September) for CO, 19% (in May-September) for O3 and 32 % (in January-April) for BC. During May-September, the analysis of the correlation among CO, O3 and BC as a function of the COant indicated that ICO-OV was influenced by air-masses rich in anthropogenic pollution transported from the regional to the global scale. On the other side, CO and O3 were negatively correlated during October-December, when FLEXPART does not show significant presence of re- cent anthropogenic emissions and only a few observations are characterized by enhanced BC. Such behaviour may be attributed to an ensemble of processes concurrent in enhancing O3 with low CO (upper troposphere/lower stratosphere intrusions) and to O3 titration by NO in polluted air-masses along with lower photochemical activity. An intermediate situation occurs in January-April when CO and O3 were almost uncorrelated and BC enhancements were associated to relatively old (10 days) anthropogenic emissions. [ABSTRACT FROM AUTHOR]

This work investigates the variability of ozone (O3), carbon monoxide (CO) and equivalent black carbon (BC) concentrations at the Italian Climate Observatory "O. Vittori" (ICO-OV), part of the Mt. Cimone global GAW-WMO station (Italy). For this purpose, ICO-OV observations carried out in the period January 2007-June 2009, have been analysed and correlated with the output of the FLEXPART Lagrangian dispersion model to specifically evaluate the influence of biomass burning (BB) and anthropogenic emissions younger than 20 days. During the investigation period, the average O3, CO and BC concentrations at ICO-OV were 54 ± 3 ppbv, 122 ± 7 ppbv and 213 ± 34 ngm-3 (mean ± expanded uncertainty with p < 95%), with clear seasonal cycles characterized by summer maxima and winter minima for O3 and BC and spring maximum and summer minimum for CO. According to FLEXPART output, BB impact is maximized during the warm months from July to September but appeared to have a significant contribution to the observed tracer concentrations only during specific transport events. We characterised in detail five major events with respect to transport scales (i.e. global, regional and local), source regions and O3, CO and BC variations. For these events, very large variability of enhancement ratios O3/CO (from -0.22 to 0.71) and BC/CO (from 2.69 to 29.83 ngm-3ppbv-1) were observed. CO related with anthropogenic emissions (COant) contributed to 17.4% of the mean CO value observed at ICO-OV, with the warm months appearing particularly affected by transport events of air-masses rich in anthropogenic pollution. The proportion of tracer variability that is described by FLEXPART COant peaked to 37% (in May-September) for CO, 19% (in May-September) for O3 and 32% (in January-April) for BC. During May-September, the analysis of the correlation among CO, O3 and BC as a function of the COant indicated that ICO-OV was influenced by air-masses rich in anthropogenic pollution transported from the regional to the global scale. On the other side, CO and O3 were negatively correlated during October-December, when FLEXPART does not show significant presence of recent anthropogenic emissions and only a few observations are characterized by enhanced BC. Such behaviour may be attributed to an ensemble of processes concurrent in enhancing O3 with low CO (upper troposphere/lower stratosphere intrusions) and O3 titration by NO in polluted air-masses along with lower photochemical activity. An intermediate situation occurs in January-April when CO and O3 were almost uncorrelated and BC enhancements were associated to relatively old (10 days) anthropogenic emissions. [ABSTRACT FROM AUTHOR]

This study presents two years of continuous observations of physical aerosol properties at the GAW-WMO global station "Nepal Climate Observatory -- Pyramid" (NCO-P, 27°57' N, 86° 48'E), sited at 5079 m a.s.l. in the high Himalayan Khumbu Valley (Nepal). Measurements of aerosol number size distribution, aerosol optical depth (AOD) and single scattering albedo (SSA) are analysed from March 2006 to February 2008. By studying the temporal variations of coarse (1 µm < Dp ≤10 µm) particle number concentration, 53 mineral Dust Transport Events (DTEs) are identified, accounting for 22.2% of the analysed data-set. Such events occurred prevalently during pre-monsoon (for 30.6% of the period) and winter (22.1%) seasons. However, uncommon cases of mineral dust transport are observed even during the monsoon season. The main sources of mineral dust reaching NCO-P are identified in the arid regions not far from the measurement site, i.e. from Tibetan Plateau, and Lot-Thar deserts, which account for 52% of the dust transport days. Moreover, a non-negligible contribution can be attributed to the Arabian Peninsula (17%) and the Indo-Gangetic Plains (16%), as indicated by three dimensional (3-D) back-trajectory analyses performed with LAGRANTO model. The observed DTEs lead to significant enhancements in the coarse aerosol number concentration (+513%) and coarse aerosol mass (+655%), as compared with average values observed in "dust-free" conditions (0.05 ± 0.11 cm-3 and 3.4 ± 3.7 µg m-3, respectively). During DTEs, SSA is higher (0.84-0.89) than on "dust-free" days (0.75-0.83), confirming the importance of this class of events as a driver of the radiative features of the regional Himalayan climate. Considering the dust events, a significant seasonal AOD increase (+37.5%) is observed in the post-monsoon, whereas lower increase (less than +11.1%) characterises the pre-monsoon and winter seasons confirming the influence of synoptic-scale mineral dust transports on the aerosol optical properties observed at NCO-P. [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]

This paper provides a detailed description of the atmospheric conditions characterizing the high Himalayas, thanks to continuous observations begun in March 2006 at the Nepal Climate Observatory-Pyramid (NCO-P) located at 5079ma.s.l. on the southern foothills of Mt. Everest, in the framework of ABC-UNEP and SHARE-Ev-K2-CNR projects. The work presents a characterization of meteorological conditions and air-mass circulation at NCO-P during the first two years of activity. The mean values of atmospheric pressure, temperature and wind speed recorded at the site were: 551 hPa, -3.0 °C, 4.7ms-1, respectively. The highest seasonal values of temperature (1.7 °C) and relative humidity (94%) were registered during the monsoon season, which was also characterized by thick clouds, present in about 80% of the afternoon hours, and by a frequency of cloud-free sky of less than 10%. The lowest temperature and relative humidity seasonal values were registered during winter, -6.3 °C and 22%, respectively, the season being characterised by mainly cloud-free sky conditions and rare thick clouds. The summer monsoon influenced rain precipitation (seasonal mean: 237 mm), while wind was dominated by flows from the bottom of the valley (S-SW) and upper mountain (N-NE). The atmospheric composition at NCO-P has been studied thanks to measurements of black carbon (BC), aerosol scattering coefficient, PM1, coarse particles and ozone. The annual behaviour of the measured parameters shows the highest seasonal values during the premonsoon (BC: 316.9 ngm-3, PM1: 3.9 μgm-3, scattering coefficient: 11.9Mm-1, coarse particles: 0.37 cm-3 and O3: 60.9 ppbv), while the lowest concentrations occurred during the monsoon (BC: 49.6 ngm-3, PM1: 0.6 μgm-3, scattering coefficient: 2.2Mm-1, and O3: 38.9 ppbv) and, for coarse particles, during the post-monsoon (0.07 cm-3). At NCO-P, the synoptic-scale circulation regimes present three principal contributions: Westerly, South-Westerly and Regional, as shown by the analysis of in-situ meteorological parameters and 5-day LAGRANTO back-trajectories. The influence of the brown cloud (AOD>0.4) extending over Indo-Gangetic Plains up to the Himalayan foothills has been evaluated by analysing the in-situ concentrations of the ABC constituents. This analysis revealed that brown cloud hot spots mainly influence the South Himalayas during the pre-monsoon, in the presence of very high levels of atmospheric compounds (BC: 1974.1 ngm-3, PM1: 23.5 μgm-3, scattering coefficient: 57.7Mm-1, coarse particles: 0.64 cm-3, O3: 69.2 ppbv, respectively). During this season 20% of the days were characterised by a strong brown cloud influence during the afternoon, leading to a 5-fold increased in the BC and PM1 values, in comparison with seasonal means. Our investigations provide clear evidence that, especially during the pre-monsoon, the southern side of the high Himalayan valleys represent a "direct channel" able to transport brown cloud pollutants up to 5000ma.s.l., where the pristine atmospheric composition can be strongly influenced. [ABSTRACT FROM AUTHOR]

The possible minimal range of reduction in snow surface albedo due to dry deposition of black carbon (BC) in the pre-monsoon period (March-May) was estimated as a lower bound together with the estimation of its accuracy, based on atmospheric observations at the Nepal Climate Observatory - Pyramid (NCO-P) sited at 5079ma.s.l. in the Himalayan region. A total BC deposition rate was estimated as 2.89 μgm-2 day-1 providing a total deposition of 266 μg m-2 for March-May at the site, based on a calculation with a minimal deposition velocity of 1.0×10-4 ms-1 with atmospheric data of equivalent BC concentration. Main BC size at NCO-P site was determined as 103.1-669.8 nm by correlation analyses between equivalent BC concentration and particulate size distributions in the atmosphere. The BC deposition from the size distribution data was also estimated. It was found that 8.7% of the estimated dry deposition corresponds to the estimated BC deposition from equivalent BC concentration data. If all the BC is deposited uniformly on the top 2-cm pure snow, the corresponding BC concentration is 26.0-68.2 μg kg-1, assuming snow density variations of 195-512 kgm-3 of Yala Glacier close to NCO-P site. Such a concentration of BC in snow could result in 2.0-5.2% albedo reductions. By assuming these albedo reductions continue throughout the year, and then applying simple numerical experiments with a glacier mass balance model, we estimated reductions would lead to runoff increases of 70-204mm of water. This runoff is the equivalent of 11.6-33.9% of the annual discharge of a typical Tibetan glacier. Our estimates of BC concentration in snow surface for pre-monsoon season is comparable to those at similar altitudes in the Himalayan region, where glaciers and perpetual snow regions begin, in the vicinity of NCO-P. Our estimates from only BC are likely to represent a lower bound for snow albedo reductions, because we used a fixed slower deposition velocity. In addition, we excluded the effects of atmospheric wind and turbulence, snow aging, dust deposition, and snow albedo feedbacks. This preliminary study represents the first investigation of BC deposition and related albedo on snow, using atmospheric aerosol data observed at the southern slope in the Himalayas. [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]

The possible minimal range of reduction in snow surface albedo due to dry deposition of black carbon (BC) in the pre-monsoon period (March-May) was estimated as a lower bound together with the estimation of its accuracy, based on atmospheric observations at the Nepal Climate Observatory-Pyramid (NCO-P) sited at 5079 m a.s.l. in the Himalayan region. We estimated a total BC deposition rate of 2.89 μg m-2 day-1 providing a total deposition of 266 μg m-2 for March-May at the site, based on a calculation with a minimal deposition velocity of 1.0×10-4 m s-1 with atmospheric data of equivalent BC concentration. Main BC size at NCO-P site was determined as 103.1-669.8 nm by correlation analysis between equivalent BC concentration and particulate size distribution in the atmosphere. We also estimated BC deposition from the size distribution data and found that 8.7% of the estimated dry deposition corresponds to the estimated BC deposition from equivalent BC concentration data. If all the BC is deposited uniformly on the top 2-cm pure snow, the corresponding BC concentration is 26.0-68.2 μg kg-1 assuming snow density variations of 195-512 kg m-3 of Yala Glacier close to NCO-P site. Such a concentration of BC in snow could result in 2.0-5.2% albedo reductions. From a simple numerical calculations and if assuming these albedo reductions continue throughout the year, this would lead to a runoff increases of 70-204 mm of water drainage equivalent of 11.6-33.9% of the annual discharge of a typical Tibetan glacier. Our estimates of BC concentration in snow surface for pre-monsoon season can be considered comparable to those at similar altitude in the Himalayan region, where glaciers and perpetual snow region starts in the vicinity of NCO-P. Our estimates from only BC are likely to represent a lower bound for snow albedo reductions, since a fixed slower deposition velocity was used and atmospheric wind and turbulence effects, snow aging, dust deposition, and snow albedo feedbacks were not considered. This study represents the first investigation about BC deposition on snow from atmospheric aerosol data in Himalayas and related albedo effect is especially the first track at the southern slope of Himalayas. [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 5079ma.s.l. below Mt. Everest. The first 10 two-year 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 ngm-3, with a standard deviation of 296.1 ngm-3. Both aerosol mass and black carbon show well defined annual cycles, with a maximum during the pre-monsoon 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 pre-monsoon 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]

South Asia is strongly influenced by the so-called Atmospheric Brown Cloud (ABC), a wide polluted layer extending from the Indian Ocean to the Himalayas during the winter and pre-monsoon seasons (November to April). This thick, grey-brown haze blanket substantially interacts with the incoming solar radiation, causing a cooling of the Earth's surface and a warming of the atmosphere, thus influencing the monsoon system and climate. In this area, the Himalayan region, particularly sensitive to climate change, offers a unique opportunity to detect global change processes and to analyse the influence of anthropogenic pollution on background atmospheric conditions through continuous monitoring activities. This paper provides a detailed description of the atmospheric conditions characterizing the high Himalayas, thanks to continuous observations begun in March 2006 at the Nepal Climate Observatory - Pyramid (NCO-P) located at 5079m a.s.l. on the southern foothills of Mt. Everest, in the framework of ABC-UNEP and SHARE-Ev-K2-CNR projects. Besides giving an overview of the measurement site and experimental activities, the work presents an in-depth characterization of meteorological conditions and air-mass circulation at NCO-P during the first two years of activity (March 2006-February 2008). The mean values of atmospheric pressure, temperature and wind speed recorded at the site were: 551 hPa, -3.0 °C, 4.7ms-1, respectively. The highest seasonal values of temperature (1.7 °C) and relative humidity (94%) were registered during the monsoon season, which was also characterized by thick clouds present in about 80% of the afternoon hours and by a frequency of cloud-free sky less than 10%. The lowest temperature and relative humidity values were registered during winter, -6.3 °C and 22%, respectively, the season being characterised by mainly cloud-free sky conditions and rare thick clouds. The summer monsoon influenced the rain precipitation (seasonal mean 237 mm), while wind was dominated by flows from the bottom of the valley (S-SW) and upper mountain (N-NE). In relation to seasonal weather conditions, the time series variability of black carbon and dust particles (optical active aerosols) and ozone (regional greenhouse gas) were analysed, as they are significant constituents of the Atmospheric Brown Cloud and strongly influence the atmospheric radiative forcing. The highest seasonal values of black carbon (BC), ozone (O3) and dust particles were observed during the pre-monsoon season (316.9 ngm-3, 60.9 ppbv, 0.37 cm-3, respectively), while the lowest concentrations occurred during the monsoon for BC and O3 (49.6 ngm-3 and 33.6 ppbv, respectively) and postmonsoon for dust particles (0.07 cm-3). The seasonal cycles of these compounds are influenced both by the local mountain wind system and by the three principal largescale circulation regimes: Westerly, South-Westerly and Regional, as shown by the analysis of in-situ meteorological parameters and 5-day LAGRANTO back-trajectories.… [ABSTRACT FROM AUTHOR]

The paper presents the first 2-years of continuous surface ozone (O3 ) observations and systematic assessment of the influence of stratospheric intrusions (SI) at the Nepal Climate Observatory at Pyramid (NCO-P; 27°57′ N, 86°48′ E), located in the Southern 5 Himalayas at 5079ma.s.l. Continuous O3 monitoring has been carried out at this GAW-WMO station in the framework of the Ev-K2-CNR SHARE and UNEP ABC projects since March 2006. Over the period March 2006-February 2008, an average O3 value of 49±12 ppbv (±1δ) was recorded, with a large annual cycle characterized by a maximum during the pre-monsoon (61±9 ppbv) and a minimum during the mon10 soon (39±10 ppbv). In general, the average O3 diurnal cycles had different shapes in the different seasons, suggesting an important interaction between the synoptic-scale circulation and the local mountain wind regime. Short-term O3 behaviour in the middle/lower troposphere (e.g. at the altitude level of NCO-P) can be significantly affected by deep SI which, representing the most important 15 natural input for tropospheric O3 , can also influence the regional atmosphere radiative forcing. To identify days possibly influenced by SI at the NCO-P, analyses were performed on in-situ observations (O3 and meteorological parameters), total column O3 data from OMI satellite and air-mass potential vorticity provided by the LAGRANTO back-trajectory model. In particular, a specially designed statistical methodology was 20 applied to the time series of the observed and modelled stratospheric tracers. On this basis, during the 2-year investigation, 14.1% of analysed days were found to be affected by SI. The SI frequency showed a clear seasonal cycle, with minimum during the summer monsoon (1.2%) and higher values during the rest of the year (21.5%). As suggested by the LAGRANTO analysis, the position of the subtropical jet stream 25 could play an important role in determining the occurrence of deep SI transport on the Southern Himalayas. In order to estimate the fraction of O3 due to air-mass transport from the stratosphere at the NCO-P, the 30 min O3 concentrations recorded during the detected SI days were analysed. In particular, in-situ relative humidity and black carbon observations were used to exclude influence from wet and polluted air-masses transported by up-valley breezes. This analysis led to the conclusion that during SI O3 significantly increased by 27.1% (+13 ppbv) with respect to periods not affected by such events. Moreover, the integral contribution 5 of SI (O3 S) to O3 at the NCO-P was also calculated, showing that 13.7% of O3 recorded at the measurement site could be attributed to SI. On a seasonal basis, the lowest SI contributions were found during the summer monsoon (less than 0.1%), while the highest were found during the winter period (24.2%). These results indicated that, during non-monsoon periods, high O3 levels could affect NCO-P during 10 SI, thus influencing the variability of tropospheric O3 over the Southern Himalayas. Being a powerful regional greenhouse gas, these results indicate that the evaluation of the current and future regional climate cannot be assessed without properly taking into account the influence of SI to tropospheric O3 in this important area. [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 5079 m 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 optically-active 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 "ramp-up" period in 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 optically-active aerosols into the Asian upper troposphere (>5000 m 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 are impacted by transport of anthropogenic aerosols which constitute the Asian brown cloud. [ABSTRACT FROM AUTHOR]

High levels of trace gas (O3 and CO) and aerosol (BC, fine and coarse particle volumes), as well as high scattering coefficient (σp) values, were recorded at the regional GAW-WMO station of Mt. Cimone (CMN, 2165 m a.s.l., Italy) during the period 26-30 August 2007. Analysis of air-mass circulation, aerosol chemical characterization and trace gas and aerosol enhancement ratios (ERs), showed that high O3 and aerosol levels were likely linked to (i) the transport of anthropogenic pollution from northern Italy, and (ii) the advection of air masses rich in mineral dust and biomass burning (BB) products from North Africa. In particular, during the advection of air masses from North Africa, the CO and aerosol levels (CO: 175 ppbv, BC: 1015 ng/m³, fine particle volume: 3.00μm³ cm-3, σp: 84.5 Mm-1) were even higher than during the pollution event (CO: 138 ppbv, BC: 733 ng/m³, fine particles volume: 1.58 μm³ cm-3, σp: 44.9 Mm-1). Moreover, despite the presence of mineral dust able to affect significantly the O3 concentration, the analysis of ERs showed that the BB event represented an efficient source of fine aerosol particles (e.g. BC), but also of the O3 recorded at CMN. In particular, the calculated O3/CO ERs (0.10-0.17 ppbv/ppbv) were in the range of values found in literature for relatively aged (2-4 days) BB plumes and suggested significant photochemical O3 production during the air-mass transport. For fine particles and σp, the calculated ERs was higher in the BB plumes than during the anthropogenic pollution events, stressing the importance of the identified BB event as a source of atmospheric aerosol able to affect the atmospheric radiation budget. These results suggest that episodes of mineral dust mobilization and wildfire emissions over North Africa could significantly influence radiative properties (as deduced from σp observations at CMN) and air quality over the Mediterranean basin and northern Italy. [ABSTRACT FROM AUTHOR]

High levels of trace gas (O3 and CO) and aerosol (BC, fine and coarse particles) concentrations, as well as high scattering coefficient (σs) values, were recorded at the regional GAW-WMO station of Mt. Cimone (MTC, 2165ma.s.l., Italy) during the period 26-30 August 2007. Analysis of air-mass circulation, aerosol chemical characterization and trace gas and aerosol emission ratios (ERs), showed that high O3 and aerosol levels were likely linked to (i) the transport of anthropogenic pollution from Northern Italy, and (ii) the advection of air masses rich in mineral dust and biomass burning (BB) products from North Africa. In particular, during the advection of air masses from North Africa, the CO and aerosol levels (CO: 175 ppbv, BC: 1015 ng/m³, fine particle: 83.8 cm-3, σs: 84.5Mm-1) were even higher than during the pollution event (CO: 138 ppbv, BC: 733 ng/m³, fine particles: 41.5 cm-3, σs: 44.9Mm-1). Moreover, despite the presence of mineral dust able to significantly affect the O3 concentration, the analysis of ERs showed that the BB event represented an efficient source of fine aerosol particles (e.g. BC), but also of the O3 recorded at MTC. The results suggest that events of mineral dust mobilization and wildfire emissions over North Africa could significantly influence radiative properties (as deduced from σs observations at MTC) and air quality over the Mediterranean basin and Northern Italy. Since in the future it is expected that wildfire and Saharan dust transport frequency could increase in the Mediterranean basin due to more frequent and severe droughts, similar events will possibly play an important role in influencing the climate and the tropospheric composition over South Europe. [ABSTRACT FROM AUTHOR]