99 research outputs found

    Zonal asymmetries in middle atmospheric ozone and water vapour derived from Odin satellite data 2001–2010

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    Stationary wave patterns in middle atmospheric ozone (O<sub>3</sub>) and water vapour (H<sub>2</sub>O) are an important factor in the atmospheric circulation, but there is a strong gap in diagnosing and understanding their configuration and origin. Based on Odin satellite data from 2001 to 2010 we investigate the stationary wave patterns in O<sub>3</sub> and H<sub>2</sub>O as indicated by the seasonal long-term means of the zonally asymmetric components O<sub>3</sub>* = O<sub>3</sub>-[O<sub>3</sub>] and H<sub>2</sub>O* = H<sub>2</sub>O-[H<sub>2</sub>O] ([O<sub>3</sub>], [H<sub>2</sub>O]: zonal means). At mid- and polar latitudes we find a pronounced wave one pattern in both constituents. In the Northern Hemisphere, the wave patterns increase during autumn, maintain their strength during winter and decay during spring, with maximum amplitudes of about 10–20 % of the zonal mean values. During winter, the wave one in O<sub>3</sub>* shows a maximum over the North Pacific/Aleutians and a minimum over the North Atlantic/Northern Europe and a double-peak structure with enhanced amplitude in the lower and in the upper stratosphere. The wave one in H<sub>2</sub>O* extends from the lower stratosphere to the upper mesosphere with a westward shift in phase with increasing height including a jump in phase at upper stratosphere altitudes. In the Southern Hemisphere, similar wave patterns occur mainly during southern spring. By comparing the observed wave patterns in O<sub>3</sub>* and H<sub>2</sub>O* with a linear solution of a steady-state transport equation for a zonally asymmetric tracer component we find that these wave patterns are primarily due to zonally asymmetric transport by geostrophically balanced winds, which are derived from observed temperature profiles. In addition temperature-dependent photochemistry contributes substantially to the spatial structure of the wave pattern in O<sub>3</sub>* . Further influences, e.g., zonal asymmetries in eddy mixing processes, are discussed

    Guidelines for the establishment of microbiological criteria for foods

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    O Grupo de Trabalho Ocorrência Microbiológica na Cadeia Alimentar (GTOMCA) do Programa PortFIR considerou de grande importância o desenvolvimento de um documento que compilasse uma seleção de legislação e de informações relativas a Critérios Microbiológicos (CM), visando apoiar e facilitar, aos operadores e entidades do setor alimentar, a sua aplicação na validação do processo de produção, na segurança e/ou higiene dos géneros alimentícios, na adesão a boas práticas de fabrico dos mesmos, e/ou, ainda, na manutenção da sua qualidade durante o seu tempo de vida útil. Deste modo, o GTOMCA desenvolveu o Guia para o estabelecimento de critérios microbiológicos em géneros alimentícios, que foi publicado em abril de 2017, contemplando a identificação, caraterísticas e propósito dos CM, os fatores a considerar para a sua definição, nomeadamente: a categoria do alimento, o microrganismo e/ou as suas toxinas, os metabolitos e a virulência, os valores limite, o plano de amostragem, o tipo de utilização e consumo assim como o método de análise laboratorial, o ponto da cadeia alimentar onde se aplica, as medidas a tomar no caso de resultados não satisfatórios e a necessidade de revisão e atualização dos CM.The Working Group on Microbiological Occurrence on the Food Chain (GTOMCA) of Por tFIR Program considered unanimously, as an important need, the existence of a document with a selection and compilation of existing legislation and information concerning microbiological criteria (CM) as a tool to suppor t and facilitate its application by operators and entities in the food sector to validate the acceptability of the production process or the food safety or hygiene, the obser vance to good manufacturing practices or the maintenance of the food quality during its lifetime. So, GTOMCA developed a Guide for the establishment of microbiological criteria in foodstuf fs, which was published in April 2017, regarding the identification, characteristics and purpose of microbiological criteria, the factors to consider for its definition, identification, characteristics and purpose of CM and, as impor tant factors to consider the food categor y, the micro-organism and its metabolites, toxins and virulence factors, the limit values, the sampling plan, the type of food consumption as well as the analy tical method for testing the food, the point of the food chain where it is applied, the measures to be taken in the event of unsatisfactor y results and the need to review and update of the CM.info:eu-repo/semantics/publishedVersio

    Seasonal and interannual variations of HCN amounts in the upper troposphere and lower stratosphere observed by MIPAS

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    We present a HCN climatology of the years 2002-2012, derived from FTIR limb emission spectra measured with the Michelson Interferometer for Passive Atmospheric Sounding (MIPAS) on the ENVISAT satellite, with the main focus on biomass burning signatures in the upper troposphere and lower stratosphere. HCN is an almost unambiguous tracer of biomass burning with a tropospheric lifetime of 5-6 months and a stratospheric lifetime of about 2 years. The MIPAS climatology is in good agreement with the HCN distribution obtained by the spaceborne ACE-FTS experiment and with airborne in situ measurements performed during the INTEX-B campaign. The HCN amounts observed by MIPAS in the southern tropical and subtropical upper troposphere have an annual cycle peaking in October-November, i.e. 1-2 months after the maximum of southern hemispheric fire emissions. The probable reason for the time shift is the delayed onset of deep convection towards austral summer. Because of overlap of varying biomass burning emissions from South America and southern Africa with sporadically strong contributions from Indonesia, the size and strength of the southern hemispheric plume have considerable interannual variations, with monthly mean maxima at, for example, 14 km between 400 and more than 700 pptv. Within 1-2 months after appearance of the plume, a considerable portion of the enhanced HCN is transported southward to as far as Antarctic latitudes. The fundamental period of HCN variability in the northern upper troposphere is also an annual cycle with varying amplitude, which in the tropics peaks in May after and during the biomass burning seasons in northern tropical Africa and southern Asia, and in the subtropics peaks in July due to trapping of pollutants in the Asian monsoon anticyclone (AMA). However, caused by extensive biomass burning in Indonesia and by northward transport of part of the southern hemispheric plume, northern HCN maxima also occur around October/November in several years, which leads to semi-annual cycles. There is also a temporal shift between enhanced HCN in northern low and mid- to high latitudes, indicating northward transport of pollutants. Due to additional biomass burning at mid- and high latitudes, this meridional transport pattern is not as clear as in the Southern Hemisphere. Upper tropospheric HCN volume mixing ratios (VMRs) above the tropical oceans decrease to below 200 pptv, presumably caused by ocean uptake, especially during boreal winter and spring. The tropical stratospheric tape recorder signal with an apparently biennial period, which was detected in MLS and ACE-FTS data from mid-2004 to mid-2007, is corroborated by MIPAS HCN data. The tape recorder signal in the whole MIPAS data set exhibits periodicities of 2 and 4 years, which are generated by interannual variations in biomass burning. The positive anomalies of the years 2003, 2007 and 2011 are caused by succession of strongly enhanced HCN from southern hemispheric and Indonesian biomass burning in boreal autumn and of elevated HCN from northern tropical Africa and the AMA in subsequent spring and summer. The anomaly of 2005 seems to be due to springtime emissions from tropical Africa followed by release from the summertime AMA. The vertical transport time of the anomalies is 1 month or less between 14 and 17 km in the upper troposphere and 8-11 months between 17 and 25 km in the lower stratosphere

    Zonal asymmetries in middle atmospheric ozone and water vapour derived from Odin satellite data 2001-2010

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    Stationary wave patterns in middle atmospheric ozone (O3) and water vapour (H2O) are an important factor in the atmospheric circulation, but there is a strong gap in diagnosing and understanding their configuration and origin. Based on Odin satellite data from 2001 to 2010 we investigate the stationary wave patterns in O3 and H2O as indicated by the seasonal long-term means of the zonally asymmetric components O*/3=O3-[O3] and H2O* =H2O-[H2O] ([O3], [H2O]: zonal means). At mid- and polar latitudes we find a pronounced wave one pattern in both constituents. In the Northern Hemisphere, the wave patterns increase during autumn, maintain their strength during winter and decay during spring, with maximum amplitudes of about 10–20% of the zonal mean values. During winter, the wave one in O*/3 shows a maximum over the North Pacific/Aleutians and a minimum over the North Atlantic/Northern Europe and a double-peak structure with enhanced amplitude in the lower and in the upper stratosphere. The wave one in H2O* extends from the lower stratosphere to the upper mesosphere with a westward shift in phase with increasing height including a jump in phase at upper stratosphere altitudes. In the Southern Hemisphere, similar wave patterns occur mainly during southern spring. By comparing the observed wave patterns in O*/3 and H2O* with a linear solution of a steady-state transport equation for a zonally asymmetric tracer component we find that these wave patterns are primarily due to zonally asymmetric transport by geostrophically balanced winds, which are derived from observed temperature profiles. In addition temperature-dependent photochemistry contributes substantially to the spatial structure of the wave pattern in O*/3. Further influences, e.g., zonal asymmetries in eddy mixing processes, are discussed

    Validation of MIPAS IMK/IAA V5R_O3_224 Ozone Profiles

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    We present the results of an extensive validation program of the most recent version of ozone vertical profiles retrieved with the IMK/IAA (Institute for Meteorology and Climate Research/Instituto de Astrofisica de Andalucia) MIPAS (Michelson Interferometer for Passive Atmospheric Sounding) research level 2 processor from version 5 spectral level 1 data. The time period covered corresponds to the reduced spectral resolution period of the MIPAS instrument, i.e., January 2005-April 2012. The comparison with satellite instruments includes all post-2005 satellite limb and occultation sensors that have measured the vertical profiles of tropospheric and stratospheric ozone: ACE-FTS, GOMOS, HALOE, HIRDLS, MLS, OSIRIS, POAM, SAGE II, SCIAMACHY, SMILES, and SMR. In addition, balloon-borne MkIV solar occultation measurements and ground-based Umkehr measurements have been included, as well as two nadir sensors: IASI and SBUV. For each reference data set, bias determination and precision assessment are performed. Better agreement with reference instruments than for the previous data version, V5R_O3_220 (Laeng et al., 2014), is found: the known high bias around the ozone vmr (volume mixing ratio) peak is significantly reduced and the vertical resolution at 35 km has been improved. The agreement with limb and solar occultation reference instruments that have a known small bias vs. ozonesondes is within 7% in the lower and middle stratosphere and 5% in the upper troposphere. Around the ozone vmr peak, the agreement with most of the satellite reference instruments is within 5 %; this bias is as low as 3% for ACE-FTS, MLS, OSIRIS, POAM and SBUV

    Methane and nitrous oxide retrievals from MIPAS-ENVISAT

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    We present the strongly revised IMK/IAA MIPAS-ENVISAT CH4 and N2O data products for the MIPAS full resolution (versions V5H_CH4_21 and V5H_N2O_21) and for the reduced resolution period (versions V5R_CH4_224, V5R_CH4_225, V5R_N2O_224 and V5R_N2O_225). Differences to older retrieval versions which are known to have a high bias are discussed. The usage of the HITRAN 2008 spectroscopic dataset leads to lower values for both gases in the lower part of the profile. The improved correction of additive radiance offsets and handling of background radiance continua allows for aerosol contributions at altitudes in the upper stratosphere and above. These changes lead to more plausible values both in the radiance offset and in the profiles of the continuum absorption coefficients. They also increase the fraction of converged retrievals. Some minor changes were applied to the constraint of the inverse problem, causing small differences in the retrieved profiles, mostly due to the relaxation of off-diagonal regularisation matrix elements for the calculation of jointly retrieved absorption coefficient profiles. Spectral microwindows have been adjusted to avoid areas with saturated spectral signatures. Jointly retrieving profiles of water vapour and nitric acid serves to compensate spectroscopic inconsistencies. We discuss the averaging kernels of the products and their vertical resolution

    MIPAS IMK/IAA CFC-11 (CCl3F) and CFC-12 (CCl2F2) Measurements: Accuracy, Precision and Long-Term Stability

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    Profiles of CFC-11 (CCl3F) and CFC-12 (CCl2F2) of the Michelson Interferometer for Passive Atmospheric Sounding (MIPAS) aboard the European satellite Envisat have been retrieved from versions MIPAS/4.61 to MI-PAS/4.62 and MIPAS/5.02 to MIPAS/5.06 level-1b data using the scientific level-2 processor run by Karlsruhe Institute of Technology (KIT), Institute of Meteorology and Climate Research (IMK) and Consejo Superior de Investigaciones Cientificas (CSIC), Instituto de Astrofisica de Andalucia (IAA). These profiles have been compared to measurements taken by the balloon-borne cryosampler, Mark IV (MkIV) and MIPAS-Balloon (MIPAS-B), the airborne MIPAS-STRatospheric aircraft (MIPAS-STR), the satellite-borne Atmospheric Chemistry Experiment Fourier transform spectrometer (ACE-FTS) and the High Resolution Dynamic Limb Sounder (HIRDLS), as well as the ground-based Halocarbon and other Atmospheric Trace Species (HATS) network for the reduced spectral resolution period (RR: January 2005-April 2012) of MIPAS. ACE-FTS, MkIV and HATS also provide measurements during the high spectral resolution period (full resolution, FR: July 2002-March 2004) and were used to validate MIPAS CFC-11 and CFC-12 products during that time, as well as profiles from the Improved Limb Atmospheric Spectrometer, ILAS-II. In general, we find that MIPAS shows slightly higher values for CFC-11 at the lower end of the profiles (below ~ 15 km) and in a comparison of HATS ground-based data and MIPAS measurements at 3 km below the tropopause. Differences range from approximately 10 to 50 pptv (~ 5-20 %) during the RR period. In general, differences are slightly smaller for the FR period. An indication of a slight high bias at the lower end of the profile exists for CFC-12 as well, but this bias is far less pronounced than for CFC-11 and is not as obvious in the relative differences between MIPAS and any of the comparison instruments. Differences at the lower end of the profile (below ~15 km) and in the comparison of HATS and MIPAS measurements taken at 3 km below the tropopause mainly stay within 10-50 pptv (corresponding to ~ 2-10% for CFC-12) for the RR and the FR period. Between similar to 15 and 30 km, most comparisons agree within 10-20 pptv (10-20 %), apart from ILAS-II, which shows large differences above similar to 17 km. Overall, relative differences are usually smaller for CFC-12 than for CFC-11. For both species -CFC-11 and CFC-12 - we find that differences at the lower end of the profile tend to be larger at higher latitudes than in tropical and subtropical regions. In addition, MIPAS profiles have a maximum in their mixing ratio around the tropopause, which is most obvious in tropical mean profiles. Comparisons of the standard deviation in a quiescent atmosphere (polar summer) show that only the CFC-12 FR error budget can fully explain the observed variability, while for the other products (CFC-11 FR and RR and CFC-12 RR) only two-thirds to three-quarters can be explained. Investigations regarding the temporal stability show very small negative drifts in MIPAS CFC-11 measurements. These instrument drifts vary between ~ 1 and 3% decade-1. For CFC-12, the drifts are also negative and close to zero up to similar to 30 km. Above that altitude, larger drifts of up to similar to 50% decade-1 appear which are negative up to similar to 35 km and positive, but of a similar magnitude, above

    Observed temporal evolution of global mean age of stratospheric air for the 2002 to 2010 period

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    An extensive observational data set, consisting of more than 106 SF6 vertical profiles distributed globally from MIPAS measurements has been condensed into monthly zonal means of mean age of air for the period September 2002 to January 2010, binned at 10^\circ latitude and 1–2 km altitude. The data were analysed with respect to their temporal variation by fitting a regression model consisting of a constant and a linear increase term, 2 proxies for the QBO variation, sinusoidal terms for the seasonal and semiannual variation and overtones for the correction of the shapes to the observed data set. The impact of subsidence of mesospheric SF6-depleted air and in-mixing into non-polar latitudes on mid-latitudinal absolute age of air and its linear increase was assessed and found to be small. The linear increase of mean age of stratospheric air was found to be positive and partly larger than the trend derived by Engel et al. (2009) for most of the Northern mid-latitudes, the middle stratosphere in the tropics, and parts of the Southern mid latitudes, as well as for the Southern polar upper stratosphere. Multi-year decrease of age of air was found for the lowermost and the upper stratospheric tropics, for parts of Southern mid-latitudes, and for the Northern polar regions. Analysis of the amplitudes and phases of the seasonal variation shed light on the coupling of stratospheric regions to each other. In particular, the Northern mid-latitude stratosphere is well coupled to the tropics, while the Northern lowermost mid-latitudinal stratosphere is decoupled, confirming the separation of the shallow branch of the Brewer-Dobson circulation from the deep branch. We suggest an overall increased tropical upwelling, together with weakening of mixing barriers, especially in the Northern Hemisphere, as a hypothetical model to explain the observed pattern of linear multi-year increase/decrease, and amplitudes and phase shifts of the seasonal variation
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