97 research outputs found

    Global tropospheric ozone trends, attributions, and radiative impacts in 1995–2017: an integrated analysis using aircraft (IAGOS) observations, ozonesonde, and multi-decadal chemical model simulations

    Get PDF
    Quantification and attribution of long-term tropospheric ozone trends are critical for understanding the impact of human activity and climate change on atmospheric chemistry but are also challenged by the limited coverage of long-term ozone observations in the free troposphere where ozone has higher production efficiency and radiative potential compared to that at the surface. In this study, we examine observed tropospheric ozone trends, their attributions, and radiative impacts from 1995–2017 using aircraft observations from the In-service Aircraft for a Global Observing System database (IAGOS), ozonesondes, and a multi-decadal GEOS-Chem chemical model simulation. IAGOS observations above 11 regions in the Northern Hemisphere and 19 of 27 global ozonesonde sites have measured increases in tropospheric ozone (950–250 hPa) by 2.7 ± 1.7 and 1.9 ± 1.7 ppbv per decade on average, respectively, with particularly large increases in the lower troposphere (950–800 hPa) above East Asia, the Persian Gulf, India, northern South America, the Gulf of Guinea, and Malaysia/Indonesia by 2.8 to 10.6 ppbv per decade. The GEOS-Chem simulation driven by reanalysis meteorological fields and the most up-to-date year-specific anthropogenic emission inventory reproduces the overall pattern of observed tropospheric ozone trends, including the large ozone increases over the tropics of 2.1–2.9 ppbv per decade and above East Asia of 0.5–1.8 ppbv per decade and the weak tropospheric ozone trends above North America, Europe, and high latitudes in both hemispheres, but trends are underestimated compared to observations. GEOS-Chem estimates an increasing trend of 0.4 Tg yr−1 of the tropospheric ozone burden in 1995–2017. We suggest that uncertainties in the anthropogenic emission inventory in the early years of the simulation (e.g., 1995–1999) over developing regions may contribute to GEOS-Chem's underestimation of tropospheric ozone trends. GEOS-Chem sensitivity simulations show that changes in global anthropogenic emission patterns, including the equatorward redistribution of surface emissions and the rapid increases in aircraft emissions, are the dominant factors contributing to tropospheric ozone trends by 0.5 Tg yr−1. In particular, we highlight the disproportionately large, but previously underappreciated, contribution of aircraft emissions to tropospheric ozone trends by 0.3 Tg yr−1, mainly due to aircraft emitting NOx in the mid-troposphere and upper troposphere where ozone production efficiency is high. Decreases in lower-stratospheric ozone and the stratosphere–troposphere flux in 1995–2017 contribute to an ozone decrease at mid-latitudes and high latitudes. We estimate the change in tropospheric ozone radiative impacts from 1995–1999 to 2013–2017 is +18.5 mW m−2, with 43.5 mW m−2 contributed by anthropogenic emission changes (20.5 mW m−2 alone by aircraft emissions), highlighting that the equatorward redistribution of emissions to areas with strong convection and the increase in aircraft emissions are effective for increasing tropospheric ozone's greenhouse effect.</p

    Energy Resolution Performance of the CMS Electromagnetic Calorimeter

    Get PDF
    The energy resolution performance of the CMS lead tungstate crystal electromagnetic calorimeter is presented. Measurements were made with an electron beam using a fully equipped supermodule of the calorimeter barrel. Results are given both for electrons incident on the centre of crystals and for electrons distributed uniformly over the calorimeter surface. The electron energy is reconstructed in matrices of 3 times 3 or 5 times 5 crystals centred on the crystal containing the maximum energy. Corrections for variations in the shower containment are applied in the case of uniform incidence. The resolution measured is consistent with the design goals

    Time-Lapse Camera Monitoring and Study of Recurrent Breaching Flow Slides in Cap Ferret, France

    No full text
    In this paper, we present a low-cost method designed to monitor recurrent breaching flow slides that impact the security of a beach. This beach, located in France at the inlet of Arcachon Bay, connects a sand spit to a tidal channel while ending at the toe of a coastal defense. Monitoring is based on capturing images and intends to add continuous information to intermittent direct observations so that triggering and influencing factors can be assessed more precisely. The method is based on time-lapse picture collection and processing. The field of view shows successive emerged manifestations of flow slide phenomena, as well as some possibly related environmental elements. On-site application for 576 days provides important indications and details on flow slide event progress and beach recovery. A simple but quantitative analysis of the influence of sand spit topographic changes is proposed as a preliminary approach of the method&rsquo;s suitability for studies of environmental processes in conjunction with coast protection

    Relations source-récepteur transcontinentales identifiées avec un modèle Lagrangien de dispersion et une analyse en clusters

    No full text
    International audienceLong range transport of pollutants has the ability to degrade air quality far from emissions sources. We describe a recently developed technique for the analysis of pollutantʼs measurements that allows the identification of systematic source-receptor relationship across an observational dataset. This technique uses a Lagrangian particles dispersion model (LPDM). LPDMs calculate retroplumes that represent potential emission sensitivity (PES) for individual measurements. The PESs can be grouped according to their similarities by using a clustering algorithm. Grouping PES can inform about the impact of various patterns of long range transport on the measurements, and has the ability to deconvolve atmospheric mixing from the impact of surface emissions. We apply our method to measurements above Siberia, and found that ~20 ppb excess carbon monoxide (CO) over background is related to long range transport of biomass burning emissions in Kazakhstan, and ~10 ppb excess CO are associated to European emissions. We highlight the advantage of our method over traditional methods for theestablishment of source-receptor relationships in longrange transport studies.Le transport des polluants à longue distance peut provoquer une dégradation de la qualité de lʼair loin des sources dʼémissions. Nous décrivons ici une technique récemment développée pour lʼanalyse des mesures de polluants, qui permet lʼidentification systématique de relations source-récepteur à travers un jeu dʼobservations. Cette technique utilise un modèle lagrangien de dispersion de particules (MLDP). Les MLDP calculent des rétropanaches qui représentent la sensibilité aux émissions potentielles (SEP) pour des mesures individuelles. Les SEP peuvent être regroupées selon leurs ressemblances en utilisant un algorithme de clustering. La classification des SEP peut informer sur lʼimpact de différents modes de transport à longue distance sur les mesures, et permet de déconvoluer le mélange atmosphérique de lʼimpact des émissions de surface. Nous appliquons notre méthode à des mesures au-dessus de la Sibérie, et constatons quʼun excès de ~ 20 ppb de monoxyde de carbone (CO) par rapport aux concentrations de fond est expliqué par le transport à longue distance dʼémissions provenant de la combustion de biomasse au Kazakhstan, et que ~10 ppb dʼexcès de CO sont associés à des émissions européennes. Nous mettons en avant lʼavantage de notre méthode par rapport aux méthodes traditionnelles pour lʼétablissement de relations source-récepteur dans les études du transport à longue distance

    Large-scale aircraft observations of ultra-fine and fine particle concentrations in the remote Siberian troposphere: New particle formation studies

    No full text
    International audienceUltra-fine particle number concentrations were measured over Siberia during two large-scale airborne measurement campaigns in April and September 2006. During both campaigns, an aircraft flew between Novosibirsk and Yakutsk, collecting every 200 km vertical profiles up to 7 km. This dataset was completed by 5 years of monthly profiles above Novosibirsk. Particle number concentration was measured in the size ranges 3–70 and 70–200 nm, along with other tracers. Free troposphere (FT) particle concentrations (N3–200) varied between 60 and 460 cm−3, inferior to boundary layer concentrations (100–7000 cm−3). In April, high concentrations of not, vert, similar500 cm−3 were observed in a polluted air mass recently uplifted at 5–6 km altitude over eastern Siberia, with no sign of significant new particle formation. In September, particle concentrations decreased with altitude, but with a steeper gradient in N70–200 compared to N3–70, the latter accounting for 90% of the total particle concentration in the free troposphere at 6–7 km altitude. Because ultra-fine particles presumably have short lifetimes, these observed particles could have been formed in situ in the clean Siberian atmosphere. Two cases of possible nucleation with high concentration and N3–70/N70–200 ratios are reported for the September campaign, in the upper troposphere and in cloud outflow in the mid-troposphere. In the seasonal analysis, a FT N3–70 maximum is found in July–August between 6 and 7 km altitude, with N3–70 accounting for not, vert, similar90% of N3–200 supporting the hypothesis of in situ formation in the FT. A secondary FT maximum of N3–70 was identified later in autumn. In the boundary layer, seasonally maximum N3–70 concentrations were found over Novosibirsk in May and September, but not in summer, possibly due to scavenging by precipitations and a large condensational sink from biomass burning aerosols. Our dataset has a limited size resolution and no speciation capability; more investigation is thus required to understand the conditions leading to in situ nucleation processes in the Siberian air shed

    Consistency of tropospheric ozone observations made by different platforms and techniques in the global databases

    No full text
    A large quantity of tropospheric ozone observations are conducted all over the world using different platforms and techniques for different purposes and goals. These observations are commonly used to derive seasonal cycles, interannual variations and long-term trends of ozone in the troposphere. In addition, they are used for comparison with three-dimensional chemistry-transport models to evaluate their performance and hence to test our current understanding of the tropospheric ozone variability. It is still challenging to provide robust tropospheric ozone trends throughout the world because of the great variability of ozone, its complex photochemical reactions, the rarity of long-term records, the diversity of measurement techniques and platforms, and the issues with data quality. In this work, we evaluated, with emphasis on the lower troposphere, the consistency of tropospheric ozone observations made by means of multiple platforms, including surface sites, sondes and regular aircraft, that are publicly available in the global databases, but excluding space-borne platforms. Concomitant observations were examined on an hourly basis (except for ±3 hours for sonde versus aircraft) for pairs of locations at less than 100-km distance. Generally, we found good agreement between sonde and surface observations. We also found that there was no need to apply any correction factor to ozonesonde observations except for Brewer–Mast sondes at Hohenpeissenberg. Because of a larger distance between the site pairs, the correlations found between the aircraft and surface measurements were poorer than those between sonde and surface measurements. However, a relatively simple wind segregation improved the agreement between the aircraft versus surface measurements. We found also that due to diurnal cycles, the sonde launching at a fixed local time led to positive or negative biases against the surface observations, suggesting that great attention should be paid to local time and diurnal variations when using ozonesonde in the analysis of seasonal cycles, long-term trends and interannual variations of lower tropospheric ozone. The comparison of surface data at Mt. Happo to regular aircraft data over Tokyo/Narita showed a relatively reasonable agreement, ensuring regionally representative ozone data sets in this region for trend analysis
    • …
    corecore