107 research outputs found

    TOMS total ozone data compared with northern latitude Dobson ground stations

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    Ozone measurements from the Total Ozone Mapping Spectrometer on the Nimbus 7 satellite are compared with ground-based measurements from five Dobson stations at northern latitudes to evaluate the accuracy of the TOMS data, particularly in regions north of 50 deg N. The measurements from the individual stations show mean differences from -2.5 percent up to plus 8.3 percent relative to TOMS measurements and two of the ground stations, Oslo and Longyearbyen, show a significant drift of plus 1.2 percent and plus 3.7 percent per year, respectively. It can be shown from nearly simultaneous measurements in two different wavelength double pairs at Oslo that at least 2 percent of the differences result from the use of the CC' wavelength double pair instead of the standard AD wavelength double pair. Since all Norwegian stations used the CC' wavelength double pair exclusively a similar error can be assumed for Tromso and Longyearbyren. A comparison between the tropospheric ozone content in TOMS data and from ECC ozonesonde measurements at Ny-Alesund and Bear Island shows that the amount of tropospheric ozone in the standard profiles used in the TOMS algorithm is too low, which leads to an error of about 2 percent in total ozone. Particularly at high solar zenith angles (greater than 80 deg), Dobson measurements become unreliable. They are up to 20 percent lower than TOMS measurements averaged over solar zenith angles of 88 deg to 89 deg

    Model studies of the meteorology and chemical composition of the troposphere over the North Atlantic during August 18-30, 1993

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    A mesoscale chemistry transport model driven by meteorological data from a numerical weather prediction model is used to calculate ozone, carbon monoxide, oxides of nitrogen, and other chemical species over the North Atlantic for a 13-days period (August 18-30, 1993). The model has a circumpolar grid so that the boundary condition problems are minimized, and the influence of North American emissions on the chemical composition of the troposphere over the North Atlantic and Europe is calculated. During the first part of the period there is a zonal flow across the North Atlantic in the free troposphere; later, there is a strong north-south as well as vertical component in the advection field. The variability in the concentrations of ozone in the free troposphere is mainly caused by dynamical processes, while the chemical modification is small over an integration time of less than two weeks. A continental plume off the North American continent extending 2000 km or more into the North Atlantic is identified toward the end of the calculation period. There is then a maximum in the concentration of ozone around 1 km above the sea surface, with a much lower concentration in the marine boundary layer close to the ocean surface. Measurements from the U.K. Meteorological Office Hercules C-130 in the free troposphere off the Atlantic Provinces, across the Atlantic Ocean, and around the Azores together with ozone soundings from the Azores, Bermuda, and Iceland were used for model comparison. The calculations indicate that in the free troposphere the initial conditions as well as the upper boundary conditions are important for ozone distribution. In the upper troposphere the net change in the chemical formation rate of ozone due to a change in the NOx concentration is quite independent of the absolute value of the ozone concentration itself and, consequently, the choice of boundary conditions for ozone is not so important in this context, In the lower troposphere the change in the net chemical formation rate of ozone, which follows from a change in the concentration of NOx, shows a marked dependence on the concentration of ozone

    Mesoscale modeling of combined aerosol and photo-oxidant processes in the Eastern Mediterranean

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    International audienceParticulate matter and photo-oxidant processes in the Eastern Mediterranean have been studied using the UAM-AERO mesoscale air quality model in conjunction with the NILU-CTM regional model. Meteorological data were obtained from the RAMS prognostic meteorological model. The modeling domain includes the eastern Mediterranean area between the Greek mainland and the island of Crete. The modeling system is applied to study the atmospheric processes in three periods, i.e. 13?16 July 2000, 26?30 July 2000 and 7?14 January 2001. The spatial and temporal distributions of both gaseous and particulate matter pollutants have been extensively studied together with the identification of major emission sources in the area. The modeling results were compared with field data obtained in the same period. The objective of the current modeling work was mainly to apply the UAM-AERO mesoscale model in the eastern Mediterranean in order to assess the performed field campaigns and determine that the applied mesoscale model is fit for this purpose. Comparison of the modeling results with measured data was performed for a number of gaseous and aerosol species. The UAM-AERO model underestimates the PM10 measured concentrations during summer and winter campaigns. Discrepancies between modeled and measured data are attributed to unresolved particulate matter emissions. Particulate matter in the area is mainly composed by sulphate, sea salt and crustal materials, and with significant amounts of nitrate, ammonium and organics. During winter the particulate matter and oxidant concentrations were lower than the summer values

    Magnetocaloric effect in pyrochlore antiferromagnet Gd2Ti2O7

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    An adiabatic demagnetization process is studied in Gd2Ti2O7, a geometrically frustrated antiferromagnet on a pyrochlore lattice. In contrast to conventional paramagnetic salts, this compound can exhibit a temperature decrease by a factor of ten in the temperature range below the Curie-Weiss constant. The most efficient cooling is observed in the field interval between 120 and 60 kOe corresponding to a crossover between saturated and spin-liquid phases. This phenomenon indicates that a considerable part of the magnetic entropy survives in the strongly correlated state. According to the theoretical model, this entropy is associated with a macroscopic number of local modes remaining gapless till the saturation field. Monte Carlo simulations on a classical spin model demonstrate good agreement with the experiment. The cooling power of the process is experimentally estimated with a view to possible technical applications. The results for Gd2Ti2O7 are compared to those for Gd3Ga5O12, a well-known material for low temperature magnetic refrigeration.Comment: 6 pages, 4 figures, accepted versio

    Field induced transitions in a kagome antiferromagnet

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    The thermal order by disorder effect in magnetic field is studied for a classical Heisenberg antiferromagnet on the kagome lattice. Using analytical arguments we predict a unique H-T phase diagram for this strongly frustrated magnet: states with a coplanar and a uniaxial triatic order parameters respectively at low and high magnetic fields and an incompressible collinear spin-liquid state at a one-third of the saturation field. We also present the Monte Carlo data which confirm existence of these phases.Comment: 4 pages, 2 figures, accepted versio

    Enhanced magnetocaloric effect in frustrated magnets

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    The magnetothermodynamics of strongly frustrated classical Heisenberg antiferromagnets on kagome, garnet, and pyrochlore lattices is examined. The field induced adiabatic temperature change (dT/dH)_S is significantly larger for such systems compared to ordinary non-frustrated magnets and also exceeds the cooling rate of an ideal paramagnet in a wide range of fields. An enhancement of the magnetocaloric effect is related to presence of a macroscopic number of soft modes in frustrated magnets below the saturation field. Theoretical predictions are confirmed with extensive Monte Carlo simulations.Comment: 7 page

    Field induced ordering in highly frustrated antiferromagnets

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    We predict that an external field can induce a spin order in highly frustrated classical Heisenberg magnets. We find analytically stabilization of collinear states by thermal fluctuations at a one-third of the saturation field for kagome and garnet lattices and at a half of the saturation field for pyrochlore and frustrated square lattices. This effect is studied numerically for the frustrated square-lattice antiferromagnet by Monte Carlo simulations for classical spins and by exact diagonalization for S=1/2S=1/2. The field induced collinear states have a spin gap and produce magnetization plateaus.Comment: 4 pages, new analytical proof the order by disorder by thermal fluctuations is adde

    Thermodynamic Study of Excitations in a 3D Spin Liquid

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    In order to characterize thermal excitations in a frustrated spin liquid, we have examined the magnetothermodynamics of a model geometrically frustrated magnet. Our data demonstrate a crossover in the nature of the spin excitations between the spin liquid phase and the high-temperature paramagnetic state. The temperature dependence of both the specific heat and magnetization in the spin liquid phase can be fit within a simple model which assumes that the spin excitations have a gapped quadratic dispersion relation.Comment: 5 figure

    Mesoscale modeling of combined aerosol and photo-oxidant processes in the eastern Mediterranean

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    International audienceParticulate matter and photo-oxidant processes in the Eastern Mediterranean have been studied using the UAM-AERO mesoscale air quality model in conjunction with the NILU-CTM regional model. Meteorological data were obtained from the RAMS prognostic meteorological model. The modeling domain includes the eastern Mediterranean area between the Greek mainland and the island of Crete. The modeling system is applied to study the atmospheric processes in three periods, i.e. 13?16 July 2000, 26?30 July 2000 and 7?14 January 2001. The spatial and temporal distributions of both gaseous and particulate matter pollutants have been extensively studied together with the identification of major emission sources in the area. The modeling results were compared with field data obtained in the same period. Comparison of the modeling results with measured data was performed for a number of gaseous and aerosol species. The UAM-AERO model underestimates the PM10 measured concentrations during summer but better comparison has been obtained for the winter data

    Modelling chemistry in the nocturnal boundary layer above tropical rainforest and a generalised effective nocturnal ozone deposition velocity for sub-ppbv NOx conditions

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    Measurements of atmospheric composition have been made over a remote rainforest landscape. A box model has previously been demonstrated to model the observed daytime chemistry well. However the box model is unable to explain the nocturnal measurements of relatively high [NO] and [O3], but relatively low observed [NO2]. It is shown that a one-dimensional (1-D) column model with simple O3 -NOx chemistry and a simple representation of vertical transport is able to explain the observed nocturnal concentrations and predict the likely vertical profiles of these species in the nocturnal boundary layer (NBL). Concentrations of tracers carried over from the end of the night can affect the atmospheric chemistry of the following day. To ascertain the anomaly introduced by using the box model to represent the NBL, vertically-averaged NBL concentrations at the end of the night are compared between the 1-D model and the box model. It is found that, under low to medium [NOx] conditions (NOx <1 ppbv), a simple parametrisation can be used to modify the box model deposition velocity of ozone, in order to achieve good agreement between the box and 1-D models for these end-of-night concentrations of NOx and O3. This parametrisation would could also be used in global climate-chemistry models with limited vertical resolution near the surface. Box-model results for the following day differ significantly if this effective nocturnal deposition velocity for ozone is implemented; for instance, there is a 9% increase in the following day’s peak ozone concentration. However under medium to high [NOx] conditions (NOx > 1 ppbv), the effect on the chemistry due to the vertical distribution of the species means no box model can adequately represent chemistry in the NBL without modifying reaction rate constants
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