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The implementation of a web GIS service platform dedicated to the management and sharing of climatological data acquired by high elevation stations is the core of the Station at High Altitude for Research on the Environment ( SHARE) GeoNetwork project, promoted by the Ev-K2 CNR Committee. The web platform basically will provide three types of services: structured metadata archive, data and results from high-altitude environments research and projects; access to high-altitude Ev-K2 CNR stations and creation of a network of existing stations; dedicated web GIS for geo-referenced data collected during the research. High elevation environmental and territorial data and metadata are catalogued in a single integrated platform to get access to the information heritage of the SHARE project, using open-source tools: Geonetwork for the metadata catalogue and web GIS resources, and the open-source Weather and Water Database ( WDB), developed by the Norwegian Meteorological Institute, for the database information system implementation. The information system is designed to have a main node, with the possibility to install relocated subsystems based on the same technology, named focal point of SHARE, which will contain metadata and data connected to the main node. In this study, a new structure of metadata for the description of the climatological stations is proposed and WDB adaptation and data preprocessing are described in detail, giving code and script samples. [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]

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]

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]

Introduction: Ensuring reliable administration and reporting of cognitive screening tests are fundamental in establishing good clinical practice and research. This study captured the rate and type of errors in clinical practice, using the Addenbrooke's Cognitive Examination-III (ACE-III), and then the reduction in error rate using a computerized alternative, the ACEmobile app., Methods: In study 1, we evaluated ACE-III assessments completed in National Health Service (NHS) clinics ( n  = 87) for administrator error. In study 2, ACEmobile and ACE-III were then evaluated for their ability to capture accurate measurement., Results: In study 1, 78% of clinically administered ACE-IIIs were either scored incorrectly or had arithmetical errors. In study 2, error rates seen in the ACE-III were reduced by 85%-93% using ACEmobile., Discussion: Error rates are ubiquitous in routine clinical use of cognitive screening tests and the ACE-III. ACEmobile provides a framework for supporting reduced administration, scoring, and arithmetical error during cognitive screening.

Rising air pollution levels in South Asia will have worldwide environmental consequences. Transport of pollutants from the densely populated regions of India, Pakistan, China, and Nepal to the Himalayas may lead to substantial radiative forcing in South Asia with potential effects on the monsoon circulation and, hence, on regional climate and hydrological cycles, as well as to dramatic impacts on glacier retreat. An improved description of particulate sources is needed to constrain the simulation of future regional climate changes. Here, the first evidence of very frequent new particle formation events occurring up to high altitudes is presented. A 16-month record of aerosol size distribution from the Nepal Climate Observatory at Pyramid (Nepal, 5,079 m above sea level), the highest atmospheric research station, is shown. Aerosol concentrations are driven by intense ultrafine particle events occurring on >35% of the days at the interface between clean tropospheric air and the more polluted air rising from the valleys. During a pilot study, we observed a significant increase of ion cluster concentrations with the onset of new particle formation events. The ion clusters rapidly grew to a 10-nm size within a few hours, confirming, thus, that in situ nucleation takes place up to high altitudes. The initiation of the new particle events coincides with the shift from free tropospheric downslope winds to thermal upslope winds from the valley in the morning hours. The new particle formation events represent a very significant additional source of particles possibly injected into the free troposphere by thermal winds.