An overview of MAP/GLOBUS NO(x)

GLOBUS NO(x) is a combined observation of nitrogen compounds by more than 20 experiments, from satellites, remote and in situ instruments on board balloons and ground observatories, within a short time period. Held in September 1985 above Southern France, the field campaign has been a technical success. Most of the observations were achieved as anticipated. NO, NO2 and relevant species and physical parameters involved in their photochemistry, were measured between 5 and 40 km at several periods of the day. A first step of data interpretation which consists of instrumental intercomparisons, is now achieved. Several systematic biases between data of various origins which have appeared in the past, are now understood and reduced. A second step which deals with atmospheric photochemistry issues like diurnal cycles and budget, is now on its way. It will be the object of a close exchange between experimenters involved in the campaign and modelers

Four years of ground-based total ozone measurements by visible spectrometry in Antarctica

Visible spectrometers SAOZ have been developed at Service d'Aeronomie for permanent ground-based ozone monitoring at all latitudes up to the polar circle in winter. Observations are made by looking at the sunlight scattered at zenith in the visible range, twice a day, at sunrise and sunset. Compared to ozone observations in the UV generally in use, visible observations in the small Chappuis bands at twilight have the advantages of being independent of stratospheric temperature, little contaminated by tropospheric ozone and multiple scattering, and of permitting observations even in winter at the polar circle. SAOZ instruments have been installed since 1988 at several stations in the Antarctic and the Arctic. More than four years data at Dumont d'Urville in Terre Adelie (67 deg S) are now available. The station is generally located at the edge of the vortex in spring and therefore the ozone hole is seen there only occasionally. The lowest values (140 DU) were reported in early October 1991. According to these first regular observations throughout the whole winter ozone seems to increase in late autumn and winter. Its decay does not start before the end of August. Although of smaller amplitude than with the previous version five data, the ratio between the groundbased and satellite/TOMS measurements displays a systematic seasonal variation correlated partly to the sun zenith angle of observations from orbit and partly to the temperature of the stratosphere. Since ground-based measurements are always made at 90 deg SZA, the SZA dependence must come from the satellite data interpretation (TOMS observations are between 43 to 88 deg SZA). The temperature dependence could be partly due to variations of ozone absorption cross-sections in the ultraviolet used by the satellite spectrometer, and partly to a systematic seasonal cycle of the air mass factor use in the interpretation of the ground based observations. However, the last contribution appears to be too small to compensate the ozone increase in winter reported by SAOZ, which is then real

PSC and volcanic aerosol routine observations in Antarctica by UV-visible ground-based spectrometry

Polar statospheric clouds (PSC) and stratospheric aerosol can be observed by ground-based UV-visible spectrometry by looking at the variation of the color of the sky during twilight. A radiative transfer model shows that reddenings are caused by high altitude (22-28 km) thin layers of scatterers, while low altitude (12-20 km) thick ones result in blueings. The color index method applied on 4 years of observations at Dumont d'Urville (67 deg S), from 1988 to 1991, shows that probably because the station is located at the edge of the vortex, dense PSC are uncommon. More unexpected is the existence of a systematic seasonal variation of the color of the twilight sky - bluer at spring - which reveals the formation of a dense scattering layer at or just above the tropopause at the end of the winter. Large scattering layers are reported above the station in 1991, first in August around 12-14 km, later in September at 22-24 km. They are attributed to volcanic aerosol from Mt Hudson and Mt Pinatubo respectively, which erupted in 1991. Inspection of the data shows that the lowest entered rapidly into the polar vortex but not the highest which remained outside, demonstrating that the vortex was isolated at 22-26 km

Qualitative modelling and analysis of regulations in multi-cellular systems using Petri nets and topological collections

In this paper, we aim at modelling and analyzing the regulation processes in multi-cellular biological systems, in particular tissues. The modelling framework is based on interconnected logical regulatory networks a la Rene Thomas equipped with information about their spatial relationships. The semantics of such models is expressed through colored Petri nets to implement regulation rules, combined with topological collections to implement the spatial information. Some constraints are put on the the representation of spatial information in order to preserve the possibility of an enumerative and exhaustive state space exploration. This paper presents the modelling framework, its semantics, as well as a prototype implementation that allowed preliminary experimentation on some applications.Comment: In Proceedings MeCBIC 2010, arXiv:1011.005

Overshooting of Clean Tropospheric Air in the Tropical Lower Stratosphere as Seen by the CALIPSO Lidar

The evolution of aerosols in the tropical upper troposphere/lower stratosphere between June 2006 and October 2009 is examined using the observations of the space borne CALIOP lidar aboard the CALIPSO satellite. Superimposed on several volcanic plumes and soot from an extreme biomass-burning event in 2009, the measurements reveal the existence of fast cleansing episodes of the lower stratosphere to altitudes as high as 20 km. The cleansing of the full 14-20km layer takes place within 1-4 months. Its coincidence with the maximum of convective activity in the southern tropics, suggests that the cleansing is the result of a large number of overshooting towers, injecting aerosol-poor tropospheric air into the lower stratosphere. The enhancements of aerosols at the tropopause level during the NH summer may be due to the same transport process but associated with intense sources of aerosols at the surface. Since, the tropospheric air flux derived from CALIOP observations during North Hemisphere winter is 5 20 times larger than the slow ascent by radiative heating usually assumed, the observations suggest that convective overshooting is a major contributor to troposphere-to-stratosphere transport with concommitant implications to the Tropical Tropopause Layer top height, chemistry and thermal structure

Solid particles in the tropical lowest stratosphere

We report in situ and remote observations proving occasional occurrence of solid particles in the tropical lowest stratosphere, 200 km from deep convective events. The particles were found during field campaigns in Southeast Brazil (49.03 W 22.36 S). They occur in the altitude range from 17.5 to 20.8 km, at temperatures up to at least 10 K above the expected frost point temperature. While stability of ice particles at these altitudes is unexpected from a theoretical point of view, it is argued that these observations are indications of tropospheric air masses penetrating into the stratosphere during convective overshoots. It is argued that the intrusion of tropospheric air must have carried a large amount of water with it, which effectively hydrated the lowest stratosphere, and consequently suppressed sublimation. This conclusion is further supported by a separate water vapor mixing ratio profile obtained at the same observation site

Ozone loss derived from balloon-borne tracer measurements in the 1999/2000 Arctic winter

Balloon-borne measurements of CFC11 (from the DIRAC in situ gas chromatograph and the DESCARTES grab sampler), ClO and O3 were made during the 1999/2000 Arctic winter as part of the SOLVE-THESEO 2000 campaign, based in Kiruna (Sweden). Here we present the CFC11 data from nine flights and compare them first with data from other instruments which flew during the campaign and then with the vertical distributions calculated by the SLIMCAT 3D CTM. We calculate ozone loss inside the Arctic vortex between late January and early March using the relation between CFC11 and O3 measured on the flights. The peak ozone loss (~1200ppbv) occurs in the 440-470K region in early March in reasonable agreement with other published empirical estimates. There is also a good agreement between ozone losses derived from three balloon tracer data sets used here. The magnitude and vertical distribution of the loss derived from the measurements is in good agreement with the loss calculated from SLIMCAT over Kiruna for the same days

Systematic stratospheric observations on the Antarctic continent at Dumont d'Urville

Results of different routine measurements performed in Dumont d'Urville (66 deg S, 140 deg E) since 1988 are presented. They include the seasonal variation of total ozone and NO2 as measured by a SAOZ UV-Visible spectrometer, Polar Stratospheric Cloud observations by a backscatter lidar and more recently, vertical ozone profiles by ECC sondes and ozone and aerosols stratospheric profiles by a DIAL lidar. The particular results of 1991 in relation with the volcanic events of Mount Pinatubo and Mount Hudson, and the position of the polar vortex over Dumont d'Urville are discussed

Retrieval of stratospheric and tropospheric BrO profiles and columns using ground-based zenith-sky DOAS observations at Harestua, 60° N

A profiling algorithm based on the optimal estimation method is applied to ground-based zenith-sky UV-visible measurements from Harestua, Southern Norway (60&deg; N, 11&deg; E) in order to retrieve BrO vertical profiles. The sensitivity of the zenith-sky observations to the tropospheric BrO detection is increased by using for the spectral analysis a fixed reference spectrum corresponding to clear-sky noon summer conditions. The information content and retrieval errors are characterized and it is shown that the retrieved stratospheric profiles and total columns are consistent with correlative balloon and satellite observations, respectively. Tropospheric BrO columns are derived from profiles retrieved at 80&deg; solar zenith angle during sunrise and sunset for the 2000&ndash;2006 period. They show a marked seasonality with mean column value ranging from 1.52&plusmn;0.62&times;10¹³ molec/cm² in late winter/early spring to 0.92&plusmn;0.38&times;10¹³ molec/cm² in summer, which corresponds to 1.0&plusmn;0.4 and 0.6&plusmn;0.2 pptv, respectively, if we assume that BrO is uniformly mixed in the troposphere. These column values are also consistent with previous estimates made from balloon, satellite, and other ground-based observations. Daytime (10:30 LT) tropospheric BrO columns are compared to the <i>p</i>-TOMCAT 3-D tropospheric chemical transport model (CTM) for the 2002&ndash;2003 period. <i>p</i>-TOMCAT shows a good agreement with the retrieved columns except in late winter/early spring where an underestimation by the model is obtained. This finding could be explained by the non-inclusion of sea-ice bromine sources in the current version of <i>p</i>-TOMCAT. Therefore the model cannot reproduce the possible transport of air-masses with enhanced BrO concentration due to bromine explosion events from the polar region to Harestua. The daytime stratospheric BrO columns are compared to the SLIMCAT stratospheric 3-D-CTM. The model run used in this study, which assumes 21.2 pptv for the Br_y loading (15 pptv for long-lived bromine species and additional 6 pptv for very short-lived species (VSLS) added by a scaling of CH₃Br), significantly underestimates the retrieved BrO columns. A sensitivity study shows that a good agreement can only be obtained if 6 to 8 pptv accounting for VSLS are added directly (and not by a scaling of CH₃Br) to the SLIMCAT long-lived bromine species profile. This contribution of the VSLS to the total bromine loading is also consistent with recently published studies

Retrieval of nitrogen dioxide stratospheric profiles from ground-based zenith-sky UV-visible observations: validation of the technique through correlative comparisons

A retrieval algorithm based on the Optimal Estimation Method (OEM) has been developed in order to provide vertical distributions of NO₂ in the stratosphere from ground-based (GB) zenith-sky UV-visible observations. It has been applied to observational data sets from the NDSC (Network for Detection of Stratospheric Change) stations of Harestua (60&deg; N, 10&deg; E) and And&#248;ya (69&deg; N, 16&deg; E) in Norway. The information content and retrieval errors have been analyzed following a formalism used for characterizing ozone profiles retrieved from solar infrared absorption spectra. In order to validate the technique, the retrieved NO₂ vertical profiles and columns have been compared to correlative balloon and satellite observations. Such extensive validation of the profile and column retrievals was not reported in previously published work on the profiling from GB UV-visible measurements. A good agreement - generally better than 25% - has been found with the SAOZ (Syst&#232;me d'Analyse par Observations Z&#233;nithales) and DOAS (Differential Optical Absorption Spectroscopy) balloons. A similar agreement has been reached with correlative satellite data from the HALogen Occultation Experiment (HALOE) and Polar Ozone and Aerosol Measurement (POAM) III instruments above 25km of altitude. Below 25km, a systematic underestimation - by up to 40% in some cases - of both HALOE and POAM III profiles by our GB profile retrievals has been observed, pointing out more likely a limitation of both satellite instruments at these altitudes. We have concluded that our study strengthens our confidence in the reliability of the retrieval of vertical distribution information from GB UV-visible observations and offers new perspectives in the use of GB UV-visible network data for validation purposes