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A hygroscopicity tandem differential mobility analyzer (HTDMA) was used to measure the water uptake (hygroscopicity) of secondary organic aerosol (SOA) formed during the chemical and photochemical oxidation of several organic precursors in a smog chamber. Electron ionization mass spectra of the non-refractory submicron aerosol were simultaneously determined with an aerosol mass spectrometer (AMS), and correlations between the two different signals were investigated. SOA hygroscopicity was found to strongly correlate with the relative abundance of the ion signal m/z 44 expressed as a fraction of total organic signal (f44). m/z 44 is due mostly to the ion fragment CO2+ for all types of SOA systems studied, and has been previously shown to strongly correlate with organic O/C for ambient and chamber OA. The analysis was also performed on ambient OA from two field experiments at the remote site Jungfraujoch, and the megacity Mexico City, where similar results were found. A simple empirical linear relation between the hygroscopicity of OA at subsaturated RH, as given by the hygroscopic growth factor (GF) or "ϰorg" parameter, and f44 was determined and is given by ϰorg = 2.2 × f44 − 0.13. This approximation can be further verified and refined as the database for AMS and HTDMA measurements is constantly being expanded around the world. The use of this approximation could introduce an important simplification in the parameterization of hygroscopicity of OA in atmospheric models, since f44 is correlated with the photochemical age of an air mass.

patent submitter:EM Microelectronic-Marin SA La présente invention concerne le domaine des commandes à distance sans fil et auto-alimentées, c'est-à-dire électriquement autonomes. Par auto-alimenté ou électriquement autonome, on comprend un dispositif non relié au réseau et n'ayant pas de batterie à changer ou à recharger périodiquement par un utilisateur, mais ayant ses propres moyens de génération d'énergie électrique en transformant de l'énergie provenant de l'environnement ou de l'énergie produite par l'utilisateur, notamment lors de l'actionnement du dispositif. Les dispositifs alimentés par des cellules photovoltaïques entrent dans cette catégorie ; toutefois cette source d'énergie nécessite de la lumière, laquelle peut faire défaut.

In this paper, we present a work that allows bidirectional communications in the 868/915 MHz ISM bands, using the power generated by energy harvesters. Our investigations show that a clear channel assessment, receive of acknowledge and resend of the message are possible within a limited, but reasonable time. The design relies on the use of low power microcontrollers and transceivers, and low energy management techniques.

One of the problems faced in the use of wireless networks in a multi-storey building is the damping effect of walls. Radio signals can be strongly attenuated, which results in poor or even impossible communication. In such cases, routers are often used to provide continuity. However, depending on the number of routers, this solution could lead to higher costs. In this paper, we present a low cost alternative. We use available modules to show how distant devices can easily be connected. We first discuss the requirements of such a connection with regards to 802.15.4 / ZigBee, and then present our hardware and software solutions.

The last years have seen an important increase in the development and proliferation of wireless technologies. This success, mostly related to mobility and the relative ease with which wireless devices can be linked (no wires needed between parties), has affected consumer as well as industrial applications. There are however many areas that are still closed to the introduction of wireless systems. Among the factors that affect wireless acceptance, one can name security and the complexity often involved in setting up networks. Unlike wired systems, the extra confidence afforded by “seen wires” is not available in wireless systems, making it difficult for the users to know if communication occurs between legitimate parties. This places wireless technology before the need to introduce simple methods to improve the set up and authentication processes. These aspects are addressed by binding methods. It is our purpose in this document to present such solutions, and especially how they can be used in 802.15.4 based networks. We will mainly focus on solutions involving optical or RFID techniques. We will also suggest some improvements where needed.

Within the WMO Global Atmosphere Watch (GAW) program continuous measurements of aerosol parameters have been performed at the Jungfraujoch high Alpine site since 1988. This measurement site is located on an exposed mountain col in the Bernese Alps, Switzerland, at 3580 meters altitude. Throughout the year the station is within clouds about 40% of the time. In warm months, the site is influenced by injection of planetary boundary layer air into the free troposphere during sunny afternoons due to thermal convection, while in winter it is usually in the undisturbed free troposphere. Several intensive field studies, named CLACE (Cloud and Aerosol Characterization Experiment), have been performed in both summer and winter within international collaborations. State-of-the-art instrumentation is employed to characterize the aerosol size distribution (Scanning Mobility Particle Sizer, SMPS; Optical Particle Counter, OPC). The University of Manchester and the Max Planck Institute in Mainz operated two Aerodyne Aerosol Mass Spectrometers (AMS) to measure the size segregated chemical composition. Other measured parameters were the hygroscopic properties of the particles (Hygroscopicity Tandem Differential Mobility Analyzer, H-TDMA), cloud microphysics (Particulate Volume Monitor, PVM; Forward Scattering Spectrometer Probe, FSSP; Cloud Particle Imager, CPI), and particle morphology (Environmental Scanning Electron Microscope, ESEM). An Air Ion Spectrometer (AIS) and an outdoor SMPS were also employed. The latter two instruments are especially well suited to measure nanometer sized particles (charged particles and sum of neutral and charged particles, respectively) in order to elucidate their formation mechanisms and rates. Different inlets are used for these instruments: A heated inlet (25°C) designed to prevent ice build-up and to evaporate cloud particles at an early stage, ensuring that the cloud condensation nuclei and/or ice nuclei are also sampled. This is called the total inlet. An interstitial inlet operated with a PM2 cyclone impactor removed all cloud droplets and ice crystals from the ambient air. Within a cloud the sampled air thus represents the interstitial (or unactivated) aerosol fraction. In addition, the Institute for Tropospheric Research (IFT) operated a Counterflow Virtual Impactor (CVI, Mertes et al., 2005). The CVI was part of a new prototype sampling system (Ice-CVI) that allows for the separation of small ice particles from large ice crystals, cloud droplets and interstitial aerosol particles. The extracted ice particles are dried airborne in the system and the remaining residual particles which correspond to the former ice nuclei were analyzed with a variety of different instruments. Differencing the response downstream of the different inlets provides insight in the fractionation of aerosol particles between the cloud phase and the interstitial phase.

Most of the current uses for ZigBee and IEEE 802.15.4 focus on control applications. However, there are other areas that will benefit from the standardisation, low cost and possibly low power of ZigBee/IEEE 802.15.4. This paper focuses on the use of ZigBee/IEEE802.15.4 for audio applications. We will discuss the advantages and theoretical limits of ZigBee/IEEE 802.15.4 for this kind of applications. We will then present a design that we used as starting point to develop applications related to the transfer of audio data.

Fog-induced visibility reduction is responsible for a variety of hazards in the transport sector. Therefore there is a large demand for an improved understanding of fog formation and thus improved forecasts. Improved fog forecasts require a better understanding of the numerous complex mechanisms during the fog life cycle. During winter 2012/13 a field campaign called ParisFog aiming at fog research took place at SIRTA (Instrumented Site for Atmospheric Remote Sensing Research). SIRTA is located about 20 km southwest of the Paris city center, France, in a semi-urban environment. In situ activation properties of the prevailing fog were investigated by measuring (1) total and interstitial (non-activated) dry particle number size distributions behind two different inlet systems; (2) interstitial hydrated aerosol and fog droplet size distributions at ambient conditions; and (3) cloud condensation nuclei (CCN) number concentration at different supersaturations (SS) with a CCN counter. The aerosol particles were characterized regarding their hygroscopic properties, fog droplet activation behavior and contribution to light scattering for 17 developed fog events. Low particle hygroscopicity with an overall median of the hygroscopicity parameter, κ, of 0.14 was found, likely caused by substantial influence from local traffic and wood burning emissions. Measurements of the aerosol size distribution at ambient RH revealed that the critical wet diameter, above which the hydrated aerosols activate to fog droplets, is rather large (with a median value of 2.6μm) and is highly variable (ranging from 1 to 5μm) between the different fog events. Thus, the number of activated fog droplets was very small and the non-activated hydrated particles were found to contribute significantly to the observed light scattering and thus to the reduction in visibility. Combining all experimental data, the effective peak supersaturation, SSpeak, a measure of the peak supersaturation during the fog formation, was determined. The median SSpeak value was estimated to be in the range from 0.031 to 0.046% (upper and lower limit estimations), which is in good agreement with previous experimental and modeling studies of fog., Atmospheric Chemistry and Physics, 14 (19), ISSN:1680-7375, ISSN:1680-7367

Cloud condensation nuclei counter (CCNC) measurements performed at 14 locations around the world within the European Integrated project on Aerosol Cloud Climate and Air Quality interactions (EUCAARI) framework have been analysed and discussed with respect to the cloud condensation nuclei (CCN) activation and hygroscopic properties of the atmospheric aerosol. The annual mean ratio of activated cloud condensation nuclei (NCCN) to the total number concentration of particles (NCN), known as the activated fraction A, shows a similar functional dependence on supersaturation S at many locations – exceptions to this being certain marine locations, a free troposphere site and background sites in south-west Germany and northern Finland. The use of total number concentration of particles above 50 and 100 nm diameter when calculating the activated fractions (A50 and A100, respectively) renders a much more stable dependence of A on S; A50 and A100 also reveal the effect of the size distribution on CCN activation. With respect to chemical composition, it was found that the hygroscopicity of aerosol particles as a function of size differs among locations. The hygroscopicity parameter κ decreased with an increasing size at a continental site in south-west Germany and fluctuated without any particular size dependence across the observed size range in the remote tropical North Atlantic and rural central Hungary. At all other locations κ increased with size. In fact, in Hyytiälä, Vavihill, Jungfraujoch and Pallas the difference in hygroscopicity between Aitken and accumulation mode aerosol was statistically significant at the 5 % significance level. In a boreal environment the assumption of a size-independent κ can lead to a potentially substantial overestimation of NCCN at S levels above 0.6 %. The same is true for other locations where κ was found to increase with size. While detailed information about aerosol hygroscopicity can significantly improve the prediction of NCCN, total aerosol number concentration and aerosol size distribution remain more important parameters. The seasonal and diurnal patterns of CCN activation and hygroscopic properties vary among three long-term locations, highlighting the spatial and temporal variability of potential aerosol–cloud interactions in various environments., Atmospheric Chemistry and Physics, 15 (21), ISSN:1680-7375, ISSN:1680-7367

Cloud condensation nuclei (CCN) number concentrations alongside with submicrometer particle number size distributions and particle chemical composition have been measured at atmospheric observatories of the Aerosols, Clouds, and Trace gases Research InfraStructure (ACTRIS) as well as other international sites over multiple years. Here, harmonized data records from 11 observatories are summarized, spanning 98,677 instrument hours for CCN data, 157,880 for particle number size distributions, and 70,817 for chemical composition data. The observatories represent nine different environments, e.g., Arctic, Atlantic, Pacific and Mediterranean maritime, boreal forest, or high alpine atmospheric conditions. This is a unique collection of aerosol particle properties most relevant for studying aerosol-cloud interactions which constitute the largest uncertainty in anthropogenic radiative forcing of the climate. The dataset is appropriate for comprehensive aerosol characterization (e.g., closure studies of CCN), model-measurement intercomparison and satellite retrieval method evaluation, among others. Data have been acquired and processed following international recommendations for quality assurance and have undergone multiple stages of quality assessment., Scientific Data, 4, ISSN:2052-4463

We discuss the major mass spectral features of different types of refractory carbona-ceous particles, ionized after laser vapourization with an Aerodyne High-ResolutionSoot-Particle Aerosol Mass Spectrometer (SP-AMS). The SP-AMS was operated witha switchable 1064 nm laser and a 600◦C thermal vapourizer, yielding respective measurements of the refractory and non-refractory particle components. Six samples wereinvestigated, all of which were composed primarily of refractory material: fuel-rich andfuel-lean propane/air diffusion-flame combustion particles; graphite-spark-generatedparticles; a commercial Fullerene-enriched Soot; Regal Black, a commercial carbonblack; and nascent aircraft-turbine combustion particles.All samples exhibited a spectrum of carbon-cluster ions Cn+xin their refractory massspectrum. Smaller clusters (x1). In all six cases, the ions C+1and C+3contributed over 60% to the total15C+15 were present. When such signalswere present, C+1/C+3was close to 1. When absent, C+1/C+3was, Atmospheric Chemistry and Physics, 13, ISSN:1680-7375, ISSN:1680-7367

This paper presents the light-scattering properties of atmospheric aerosol particles measured over the past decade at 28 ACTRIS observatories, which are located mainly in Europe. The data include particle light scattering (sp) and hemispheric backscattering (bsp) coefficients, scattering Ångström exponent (SAE), backscatter fraction (BF) and asymmetry parameter (g). An increasing gradient of sp is observed when moving from remote environments (arctic/mountain) to regional and to urban environments. At a regional level in Europe, sp also increases when moving from Nordic and Baltic countries and from western Europe to central/eastern Europe, whereas no clear spatial gradient is observed for other station environments. The SAE does not show a clear gradient as a function of the placement of the station. However, a west-to-east-increasing gradient is observed for both regional and mountain placements, suggesting a lower fraction of fine-mode particle in western/south-western Europe compared to central and eastern Europe, where the fine-mode particles dominate the scattering. The g does not show any clear gradient by station placement or geographical location reflecting the complex relationship of this parameter with the physical properties of the aerosol particles. Both the station placement and the geographical location are important factors affecting the intraannual variability. At mountain sites, higher sp and SAE values are measured in the summer due to the enhanced boundary layer influence and/or new particle-formation episodes. Conversely, the lower horizontal and vertical dispersion during winter leads to higher sp values at all low-altitude sites in central and eastern Europe compared to summer. These sites also show SAE maxima in the summer (with corresponding g minima). At all sites, both SAE and g show a strong variation with aerosol particle loading. The lowest values of g are always observed together with low sp values, indicating a larger contribution from particles in the smaller accumulation mode. During periods of high sp values, the variation of g is less pronounced, whereas the SAE increases or decreases, suggesting changes mostly in the coarse aerosol particle mode rather than in the fine mode. Statistically significant decreasing trends of sp are observed at 5 out of the 13 stations included in the trend analyses. The total reductions of sp are consistent with those reported for PM2:5 and PM10 mass concentrations over similar periods across Europe.

Aerosol–cloud interactions (ACI) constitute the single largest uncertainty in anthropogenic radiative forcing. To reduce the uncertainties and gain more confidence in the simulation of ACI, models need to be evaluated against observations, in particular against measurements of cloud condensation nuclei (CCN). Here we present a data set – ready to be used for model validation – of long-term observations of CCN number concentrations, particle number size distributions and chemical composition from 12 sites on 3 continents. Studied environments include coastal background, rural background, alpine sites, remote forests and an urban surrounding. Expectedly, CCN characteristics are highly variable across site categories. However, they also vary within them, most strongly in the coastal background group, where CCN number concentrations can vary by up to a factor of 30 within one season. In terms of particle activation behaviour, most continental stations exhibit very similar activation ratios (relative to particles >20 nm) across the range of 0.1 to 1.0% supersaturation. At the coastal sites the transition from particles being CCN inactive to becoming CCN active occurs over a wider range of the supersaturation spectrum. Several stations show strong seasonal cycles of CCN number concentrations and particle number size distributions, e.g. at Barrow (Arctic haze in spring), at the alpine stations (stronger influence of polluted boundary layer air masses in summer), the rain forest (wet and dry season) or Finokalia (wildfire influence in autumn). The rural background and urban sites exhibit relatively little variability throughout the year, while short-term variability can be high especially at the urban site. The average hygroscopicity parameter, , calculated from the chemical composition of submicron particles was highest at the coastal site of Mace Head (0.6) and lowest at the rain forest station ATTO (0.2–0.3).We performed closure studies based on –Köhler theory to predict CCN number concentrations. The ratio of predicted to measured CCN concentrations is between 0.87 and 1.4 for five different types of . The temporal variability is also well captured, with Pearson correlation coefficients exceeding 0.87. Information on CCN number concentrations at many locations is important to better characterise ACI and their radiative forcing. But long-term comprehensive aerosol particle characterisations are labour intensive and costly. Hence, we recommend operating “migrating-CCNCs” to conduct collocated CCN number concentration and particle number size distribution measurements at individual locations throughout one year at least to derive a seasonally resolved hygroscopicity parameter. This way, CCN number concentrations can only be calculated based on continued particle number size distribution information and greater spatial coverage of longterm measurements can be achieved.

Aerosols influence the Earth's radiation budget directly through absorption and scattering of solar radiation in the atmosphere but also indirectly by modifying the properties of clouds. However, climate models still suffer from large uncertainties as a result of insufficient understanding of aerosol-cloud interactions. At the high altitude research station Jungfraujoch (JFJ; 3580 m a.s.l., Switzerland) cloud condensation nuclei (CCN) number concentrations at eight different supersaturations (SS) from 0.24% to 1.18% were measured using a CCN counter during Summer 2011. Simultaneously, in-situ aerosol activation properties of the prevailing ambient clouds were investigated by measuring the total and interstitial (non-activated) dry particle number size distributions behind two different inlet systems. Combining all experimental data, a new method was developed to retrieve the so-called effective peak supersaturation SSpeak, as a measure of the SS at which ambient clouds are formed. A 17-month CCN climatology was then used to retrieve the SSpeak values also for four earlier summer campaigns (2000, 2002, 2004 and 2010) where no direct CCN data were available. The SSpeak values varied between 0.01% and 2.0% during all campaigns. An overall median SSpeak of 0.35% and dry activation diameter of 87 nm was observed. It was found that the difference in topography between northwest and southeast plays an important role for the effective peak supersaturation in clouds formed in the vicinity of the JFJ, while differences in the number concentration of potential CCN only play a minor role. Results show that air masses coming from the southeast (with the slowly rising terrain of the Aletsch Glacier) generally experience lower SSpeak values than air masses coming from the northwest (steep slope). The observed overall median values were 0.41% and 0.22% for northwest and southeast wind conditions, respectively, corresponding to literature values for cumulus clouds and shallow-layer clouds. These cloud types are consistent with weather observations routinely performed at the JFJ., Atmospheric Chemistry and Physics, 14 (2), ISSN:1680-7375, ISSN:1680-7367

The volcanic aerosol plume resulting from the Eyjafjallajökull eruption in Iceland in April and May 2010 was detected in clear layers above Switzerland during two periods (17–19 April 2010 and 16–19 May 2010). In-situ measurements of the airborne volcanic plume were performed both within ground-based monitoring networks and with a research aircraft up to an altitude of 6000 m a.s.l. The wide range of aerosol and gas phase parameters studied at the high altitude research station Jungfraujoch (3580 m a.s.l.) allowed for an in-depth characterization of the detected volcanic aerosol. Both the data from the Jungfraujoch and the aircraft vertical profiles showed a consistent volcanic ash mode in the aerosol volume size distribution with a mean optical diameter around 3 ± 0.3 μm. These particles were found to have an average chemical composition very similar to the trachyandesite-like composition of rock samples collected near the volcano. Furthermore, chemical processing of volcanic sulfur dioxide into sulfate clearly contributed to the accumulation mode of the aerosol at the Jungfraujoch. The combination of these in-situ data and plume dispersion modeling results showed that a significant portion of the first volcanic aerosol plume reaching Switzerland on 17 April 2010 did not reach the Jungfraujoch directly, but was first dispersed and diluted in the planetary boundary layer. The maximum PM10 mass concentrations at the Jungfraujoch reached 30 μgm−3 and 70 μgm−3 (for 10-min mean values) duri ng the April and May episode, respectively. Even low-altitude monitoring stations registered up to 45 μgm−3 of volcanic ash related PM10 (Basel, Northwestern Switzerland, 18/19 April 2010). The flights with the research aircraft on 17 April 2010 showed one order of magnitude higher number concentrations over the northern Swiss plateau compared to the Jungfraujoch, and a mass concentration of 320 (200–520) μgm−3 on 18 May 2010 over the northwestern Swiss plateau. The presented data significantly contributed to the time-critical assessment of the local ash layer properties during the initial eruption phase. Furthermore, dispersion models benefited from the detailed information on the volcanic aerosol size distribution and its chemical composition., Atmospheric Chemistry and Physics, 11 (19), ISSN:1680-7375, ISSN:1680-7367

We discuss the major mass spectral features of different types of refractory carbonaceous particles, ionized after laser vaporization with an Aerodyne high-resolution soot-particle aerosol mass spectrometer (SP-AMS). The SP-AMS was operated with a switchable 1064 nm laser and a 600 °C thermal vaporizer, yielding respective measurements of the refractory and non-refractory particle components. Six samples were investigated, all of which were composed primarily of refractory material: fuel-rich and fuel-lean propane/air diffusion-flame combustion particles; graphite-spark-generated particles; a commercial fullerene-enriched soot; Regal Black, a commercial carbon black; and nascent aircraft-turbine combustion particles. All samples exhibited a spectrum of carbon-cluster ions Cxn+ in their refractory mass spectrum. Smaller clusters (x < 6) were found to dominate the Cxn+ distribution. For fullerene soot, fuel-rich-flame particles and spark-generated particles, significant Cxn+ clusters at x ≫ 6 were present, with significant contributions from multiply charged ions (n > 1). In all six cases, the ions C1+ and C3+ contributed over 60% to the total C1+ intensity. Furthermore, the ratio of these major ions C1+ / C3+ could be used to predict whether significant Cxn+ signals with x > 5 were present. When such signals were present, C1+ / C3+ was close to 1. When absent, C1+ / C3+ was < 0.8. This ratio may therefore serve as a proxy to distinguish between the two types of spectra in atmospheric SP-AMS measurements. Significant refractory oxygenated ions such as CO+ and CO2+ were also observed for all samples. We discuss these signals in detail for Regal Black, and describe their formation via decomposition of oxygenated moieties incorporated into the refractory carbon structure. These species may be of importance in atmospheric processes such as water uptake and heterogeneous chemistry. If atmospherically stable, these oxidized species may be useful for distinguishing between different combustion sources. If unstable, they may provide a means to estimate the atmospheric age of an rBC sample. Future studies should attempt to establish which of these scenarios is more realistic., Atmospheric Chemistry and Physics, 14 (5), ISSN:1680-7375, ISSN:1680-7367