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The Match method for the quantification of polar chemical ozone loss is investigated mainly with respect to the impact of the transport of air masses across the vortex edge. For the winter 2002/03, we show that significant transport across the vortex edge occurred and was simulated by the Chemical Lagrangian Model of the Stratosphere. In-situ observations of inert tracers and ozone from HAGAR on the Geophysica aircraft and balloon-borne sondes, and remote observations from MIPAS on the ENVISAT satellite were reproduced well by CLaMS. The model even reproduced a small vortex remnant that remained a distinct feature until June 2003 and was also observed in-situ by a balloon-borne whole air sampler. We use this CLaMS simulation to quantify the impact of transport across the vortex edge on ozone loss estimates from the Match method. We show that a time integration of the determined vortex average ozone loss rates, as performed in Match, results in a larger ozone loss than the polar vortex average ozone loss in CLaMS. The determination of the Match ozone loss rates is also influenced by the transport of air across the vortex edge. We use the model to investigate how the sampling of the ozone sondes on which Match is based represents the vortex average ozone loss rate. Both the time integration of ozone loss and the determination of ozone loss rates for Match are evaluated using the winter 2002/2003 CLaMS simulation. These impacts can explain the majority of the differences between CLaMS and Match column ozone loss. While the investigated effects somewhat reduce the apparent discrepancy in January ozone loss rates reported earlier, a distinct discrepancy between simulations and Match remains. However, its contribution to the accumulated ozone loss over the winter is not large.
The total stratospheric organic chlorine and bromine burden was derived from balloon-borne measurements in the tropics (Teresina, Brazil, 5°04´ S, 42°52´ W) in 2005. Whole air samples were collected cryogenically at altitudes between 15 and 34 km. For the first time, we report measurements of a set of 28 chlorinated and brominated substances in the tropical upper troposphere and stratosphere including ten substances with an atmospheric lifetime of less than half a year. The substances were quantified using pre-concentration techniques followed by Gas Chromatography with Mass Spectrometric detection. In the tropical tropopause layer at altitudes between 15 and 17 km we found 1.1–1.4% of the chlorine and 6–8% of the bromine to be present in the form of very short-lived organic compounds. By combining the data with tropospheric reference data and age of air observations the abundances of inorganic chlorine and bromine (Cly and Bry) were derived. At an altitude of 34 km we calculated 3062 ppt of Cly and 17.5 ppt of Bry from the decomposition of both long- and short-lived organic source gases. Furthermore we present indications for the presence of additional organic brominated substances in the tropical upper troposphere and stratosphere.
During the second part of the TROCCINOX campaign that took place in Brazil in early 2005, chemical species were measured on-board the high-altitude research aircraft Geophysica (ozone, water vapor, NO, NOy, CH4 and CO) in the altitude range up to 20 km (or up to 450 K potential temperature), i.e. spanning the entire TTL region roughly extending between 350 and 420 K. Here, analysis of transport across the TTL is performed using a new version of the Chemical Lagrangian Model of the Stratosphere (CLaMS). In this new version, the stratospheric model has been extended to the earth surface. Above the tropopause, the isentropic and cross-isentropic advection in CLaMS is driven by meteorological analysis winds and heating/cooling rates derived from a radiation calculation. Below the tropopause, the model smoothly transforms from the isentropic to the hybrid-pressure coordinate and, in this way, takes into account the effect of large-scale convective transport as implemented in the vertical wind of the meteorological analysis. As in previous CLaMS simulations, the irreversible transport, i.e. mixing, is controlled by the local horizontal strain and vertical shear rates. Stratospheric and tropospheric signatures in the TTL can be seen both in the observations and in the model. The composition of air above ≈350 K is mainly controlled by mixing on a time scale of weeks or even months. Based on CLaMS transport studies where mixing can be completely switched off, we deduce that vertical mixing, mainly driven by the vertical shear in the tropical flanks of the subtropical jets and, to some extent, in the the outflow regions of the large-scale convection, offers an explanation for the upward transport of trace species from the main convective outflow at around 350 K up to the tropical tropopause around 380 K.
The ENVISAT validation programme for the atmospheric instruments MIPAS, SCIAMACHY and GOMOS is based on a number of balloon-borne, aircraft, satellite and ground-based correlative measurements. In particular the activities of validation scientists were coordinated by ESA within the ENVISAT Stratospheric Aircraft and Balloon Campaign or ESABC. As part of a series of similar papers on other species [this issue] and in parallel to the contribution of the individual validation teams, the present paper provides a synthesis of comparisons performed between MIPAS CH4 and N2O profiles produced by the current ESA operational software (Instrument Processing Facility version 4.61 or IPF v4.61, full resolution MIPAS data covering the period 9 July 2002 to 26 March 2004) and correlative measurements obtained from balloon and aircraft experiments as well as from satellite sensors or from ground-based instruments. In the middle stratosphere, no significant bias is observed between MIPAS and correlative measurements, and MIPAS is providing a very consistent and global picture of the distribution of CH4 and N2O in this region. In average, the MIPAS CH4 values show a small positive bias in the lower stratosphere of about 5%. A similar situation is observed for N2O with a positive bias of 4%. In the lower stratosphere/upper troposphere (UT/LS) the individual used MIPAS data version 4.61 still exhibits some unphysical oscillations in individual CH4 and N2O profiles caused by the processing algorithm (with almost no regularization). Taking these problems into account, the MIPAS CH4 and N2O profiles are behaving as expected from the internal error estimation of IPF v4.61 and the estimated errors of the correlative measurements.
In the Maizuru zone nearly whole the Triassic successions are developed. The Scythian to Aniso-Ladinian strata make a continuous sequence, in which are distinguished three faunizones, Neoschizous-"Bakevellia", Hollandites-"Danubites" and Monophyllites, corresponding to Scythian, lower Anisian and Aniso-Ladinian, respectively. Main portion of the Ladinian series is lacking in this region. The earliest Carnian or Ladino-Carnian Arakuran age is newly proposed founded on the palaeontological and stratigraphical studies on the Arakura formation. In the next Sakawan (not Carnian) Nabae group, two and probably one more, faunizones are recognizable, Palaeopharus-Lima yataensis, Tosapecten-Pseudolimea, and Pleuromya-Neoschizodus. The Sakawan age is classified into two subages better than the three formerly proposed by K. ICHIKAWA. The Norian sediments are probably represented by the Nakaiso conglomerate bed, although barren in fossil. The Rhaetic strata are not found at all like other regions in Japan. From the facies-analysis, the Palaeo-Maizuru Bay during the Scythian to Aniso-Ladinian epochs and the Palaeo-Maizuru Inland Sea during the Carnian epoch are assumed. Finally, the orogenic history of the Triassic period in this zone is briefly stated.
The Tanzawa mountainland consists of a pyroclastic complex chiefly of basic composition which is intruded by a large mass of quartz-diorite at the center. This complex, well-known as the Misaka series, is the products of largescale geosynclinal volcanisms which took place during the period from the latest Oligocene to the middle Miocene in age. As compared with other geologic units, the present complex is characterized by its unusually thick accumulation of pyroclastic rocks, and by the intense hydrothermal alteration of the rocks, furnishing us an excellent section of the so-called green tuff series in the southeastern region of the Fossa Magna. Also the development of the products of interesting metamorphism of the quartz-diorite to the surrounding pyroclastic rocks is a feature uncommon in the other green tuff series of the above region. The crustal movement occurring during the volcanisms, however, make the structure of this complex highly complicate. In addition, the topographically unfavourable condition of this mountainland causes great hindrance to the geological investigation of this complex. Accordingly, the true natures of the complex remain unknown both stratigraphically and petrographically. Since 1948, the writer has been studying on the complex distributed in the eastern region of the Tanzawa massif from the volcano-stratigraphical point of view, some of the results of which have been published as miscellaneous reports. The main scope of this paper is to describe the stratigraphy, petrography, and the tectonic history of this complex. In this paper are also discussed the characteristics of the volcanic activities and the alterations represented by the same complex.
Die Insel Zante
(1891)