Spatial dispersion of Faraday rotation and its connexion with mode coupling

It is shown that the lack of linear polarization in the microwave radiation of solar bursts (reported in a earlier paper) may be explained by spatial dispersion of Faraday rotation. The maximum source diameter s without noticeable destruction of linear polarization is determined by the electron density and the magnetic field strength in the volume, where the linear polarization is generated. In the case where linear polarization is produced by the radiation source, s is smaller than only 20 km. In the other case where linear polarization is produced by mode coupling in a quasi-transverse magnetic field in the corona, the s-values are found to range from 10 to 6000 km, which is still much smaller than the generally adopted sizes of microwave burst sources. The second case has been investigated for several models of magnetic fields.     

Analysis and interpretation of soft X-ray photographs of coronal active regions taken with Fresnel zone plates

Soft X-ray photographs of the Sun taken at O vii 21.6 Å and in a spectral band ranging from 13.2 to 22.1 Å have been analysed in order to establish spatially resolved maps of temperature and emission measure for several active regions in the corona. The photographs were taken on 11 March, 1971, and on 2 March, 1972, with Fresnel zone plate cameras which were flown on ESRO and NRL sounding rockets.In Part I of this paper we first deal with those aspects of the instrumentation which are important for setting up a suitable image analysis procedure. We discuss the characteristics of the wavelength dependent image formation by zone plates combined with absorption filters. Results of the calibration of the X-ray film are given. Then we describe a specific iterative data reduction procedure and finally present the resulting maps of temperature and emission measure for a selected active region. In Part II corresponding results for further active regions will be given and discussed.     

A field survey of chemicals and biological products used in shrimp farming

This study documented the use of chemicals and biological products in marine and brackish water shrimp farming in Thailand, the world's top producer of farmed shrimp. Interviews were conducted with 76 shrimp farmers in three major shrimp producing regions, the eastern Gulf coast, the southern Gulf coast and the Andaman coast area. Farmers in the study used on average 13 different chemicals and biological products. The most commonly used products were soil and water treatment products, pesticides and disinfectants. Farmers in the southern Gulf coast area used a larger number of products than farmers in the other two areas. In the study, the use of more than 290 different chemicals and biological products was documented. Many of the pesticides, disinfectants and antibiotics used by the farmers could have negative effects on the cultured shrimps, cause a risk for food safety, occupational health, and/or have negative effects on adjacent ecosystems. Manufacturers and retailers of the products often neglected to provide farmers with necessary information regarding active ingredient and relevant instructions for safe and efficient use.     

Dating the exhumation of UHP rocks and associated crustal melting in the Norwegian Caledonides

U–Pb and Rb–Sr dating was undertaken in combination with P–T estimates to (1) constrain the time of ultrahigh-pressure (UHP) eclogite formation in the Stadlandet UHP province of Norway, (2) date later crustal melting–migmatization of the eclogite country gneisses, and (3) temporally trace post-migmatite cooling and retrogression under amphibolite facies metamorphic conditions. In contrast to earlier U–Pb studies which used accessory minerals from the gneisses, we focused on the direct dating of minerals defining the HP assemblage. For the eclogite, rutile and omphacite fractions were analyzed for U–Pb, and from an adjacent migmatite leucosome titanites and K-feldspar. For Rb–Sr dating, phengite was measured for the eclogite, and biotite for two leucosome layers of the migmatite–eclogite complex. A U–Pb age of 389±7 (2σ) Ma is obtained if the full set of 12 rutile and five omphacite analyses is regressed (MSWD: 16), and 389±2 Ma for those nine data which strictly satisfy isochron conditions (MSWD: 0.78). The 389-Ma age is interpreted to date equilibration and freezing of the eclogite paragenesis at maximum temperatures of 770 °C, reached during decompression to 1.8 GPa. Decompression from 2.8 to 1.8 GPa occurred in the partial melting domain of granitic crust, with the migmatites being dated at 375±6 Ma by titanite and K-feldspar from an eclogite-adjacent granitic leucosome. This titanite age also shows that the U–Pb chronometer in rutile is very robust to high temperatures—it remained a closed system for at least 14 million years, at temperatures in excess to 650 °C. After decompression and migmatization, exhumation is accompanied by rapid cooling to reach the 300 °C isograde by 357± 9 Ma, determined by a biotite isochron for a leucosome in a slightly shallower structural level. In considering that the time of maximum pressure is bracketed by early zircon crystallization during subduction and later omphacite–rutile equilibration in the eclogites, an exhumation rate of 5 mm/year is deduced for initial exhumation, occurring between 394 and 389 Ma. For subsequent cooling from 770 to 600 °C, we obtain a rate of 2.3±1.3 mm/year. First stages of exhumation most likely occurred under an overall compressional regime, whereas Devonian basin formation is associated to detachment movements during 389–375 Ma exhumation. This period of extension is followed by a much younger, decoupled thermal phase at 327±5 Ma, occurring under static conditions within very restricted zones, most likely in association with the circulation of fluid phases along old discontinuities. Initial isotopic signatures of Sr and Pb substantiate Paleo- to Meso-Proterozoic crust formation times of the Stadlandet UHP province precursor lithologies.     

Fate and effects of polydimethylsiloxane (PDMS) in marine environments

Polydimethylsiloxanes (PDMS) defoamers are used to improve process efficiency under extreme conditions during gas-oil separation, when other chemicals fail to perform. They are also used to reduce the oil content of process waters discharged to the marine environment, thereby serving an important function in reducing oil pollution. As a consequence of these applications small quantities of PDMS may also be released into the environment. This paper reviews the fate of PDMS in the marine environment and the extensive effect studies that have been conducted. These demonstrate the absence of adverse effects on a wide range of marine species.