Ongonite from Ongon Khairkhan,Mongolia

Summary Albite-topaz kerotophyres, termed ongonites, were discovered byV. I. Kovalenko and coworkers at Ongon Khairkhan in Mongolia in 1970. The type area was revisited, described, resampled, the new data is compared with the earlier data and that from similar rocks elsewhere (Beauvoir and Cinovec granites; Macusani glass).Ongonites are fluorine-rich peraluminous sodic two feldspar granitoids with orthoclase and albite phenocrysts, high modal and normative albite content and the presence of topaz as common accessory mineral. They contain variable amounts of lithium micas or muscovite. Chemically, ongonite is similar to highly fractionated S-type or ilmenite series granitoids. In the type area, F-rich water-poor ongonite melts have intruded to a high crustal level.Ongonite displays a long history of subsolidus reactions and hydrothermal alteration. The hydrothermal alteration may be linked to a spatially associated quartz-wolframite stockwork not genetically related to ongonite. Ongonite has a low W content and an elevated Sn content despite a lack of association with Sn deposits.

---

Ongonite von Ongon Khairkhan, Mongolei

Zusammenfassung Albit-Topas-Keratophyre, auch als Ongonite bezeichnet, wurden 1970 von V. E. Kowalenko und Mitarbeitern bei Ongon Khairkhan in der Mongolei entdeckt. Die TypLokalität wurde beschrieben und beprobt und die neuen Daten werden mit den früher erhaltenen, und denen von ähnlichen Gesteinen in anderen Bereichen (die Granite von Beauvoir und Cinovec, das Glas von Macusani) verglichen.Ongonite sind Fluor- und Aluminiumreiche (Peraluminous), zwei-Feldspat-Natriumgranitoide mit idiomorphen Orthoklasen und Albit, hohem modalem und normativem Albitgehalt, und Topas als verbreitetem Nebenmineral. Sie führen wechselnde Gehalte von Lithiumglimmern oder Muskovit. Chemisch sind Ongonite stark fraktionierten S-Typ Granitoiden vergleichbar oder auch Granitoiden der Ilmenit-Serie. Im Gebiet der Typlokalität sind fluorreiche wasserarme Ongonit-Schmelzen in ein hohes Krustenniveau intrudiert worden.Ongonite zeigen eine lange Geschichte von Subsolidusreaktionen und hydrothermaler Umwandlung. Die hydrothermale Umwandlung kann mit einem räumlich assoziiertem Quarz-Wolframit Stockwerk in Beziehung gesetzt werden, das genetisch nicht mit den Ongoniten zusammenhängt. Ongonit hat einen niedrigen Wolframgehalt und einen erhöhten Zinngehalt, obwohl keine Assoziation mit Zinnlagerstätten zu beobachten ist.

     

Unusual coronal activity following the flare of 6 November 1980

For almost 30 hr after the major (gamma-ray) two-ribbon flare on 6 November 1980, 03:30 UT, the Hard X-Ray Imaging Spectrometer (HXIS) aboard the SMM satellite imaged in > 3.5 keV X-rays a gigantic arch extending above the active region over the limb. Like a similar configuration on 22 May 1980, this arch formed the lowest part of a stationary post-flare radio noise storm recorded at metric wavelengths at Nançay and Culgoora. 6.5 hr after the flare a coronal region below the arch started quasi-periodic pulsations in X-ray brightness, observed by several SMM instruments. These brightness variations had no response in the chromosphere (H), very little in the transition layer (O v), but they clearly correlated with similar variations in brightness at 169 MHz. There were 13 pulses of this kind, with apparent periodicity of about 20 min, until another flare occurred in the active region at 15:00 UT. All the brightenings appeared within a localized area of about 30000 km² in the northern part of the active region, but they definitely did not occur all at the same place.The top of the X-ray arch, at an altitude of 155 000 km, was continuously and smoothly decaying, taking no part in the striking variations below it. Therefore, the area variable in brightness does not seem to be the footpoint of the arch, as we supposed for similar variations on 22 May. More likely, it is a separate region connected directly with the source of the radio storm; particles accelerated in the storm may be dumped into the low corona and cause the X-ray enhancements. The X-ray arch was enhanced by two orders of magnitude in 3.5–5.5 keV X-ray counts and the temperature increased from 7.3 × 10⁶ to 9 × 10⁶ K when the new two-ribbon flare occurred at 15:00 UT. Thus, it is possible that energy is brought into the arch via the upper parts of the reconnecting flare loops - a process that can continue for hours.     

Forecasting ozone concentrations in the east of Croatia using nonparametric Neural Network Models

Ozone is one of the most significant secondary pollutants with numerous negative effects on human health and environment including plants and vegetation. Therefore, more effort is made recently by governments and associations to predict ozone concentrations which could help in establishing better plans and regulation for environment protection. In this study, we use two Artificial Neural Network based approaches (MPL and RBF) to develop, for the first time, accurate ozone prediction models, one for urban and another one for rural area in the eastern part of Croatia. The evaluation of actual against the predicted ozone concentrations revealed that MLP and RBF models are very competitive for the training and testing data in the case of Kopa?ki Rit area whereas in the case of Osijek city, MLP shows better evaluation results with 9% improvement in the correlation coefficient. Furthermore, subsequent feature selection process has improved the prediction power of RBF network.     

The iron-tungsten-sulphur system and its geological application

The subsolidus region of the Fe-W-S system was studied by experiments performed in evacuated silica tubes. Ternary phases were not encountered. Tungsten disulphide WS₂ is stable with the iron sulphides but not with metallic iron. The major tie-line pyrrhotite-tungsten differentiates this system from the analogous Fe-Mo-S system. Experiments on the Fe-W-O-S system demonstrate that WS₂ (tungstenite) is not stable in the presence of iron oxides. Molybdenum and tungsten show different affinities to sulphur which is manifested in nature in abundant molybdenite as contrasted with rare tungstenite. Sulphur fugacity data in the literature differ on WS₂. There data are compared with the present experimental results.

---

Zusammenfassung Das ternäre System Fe-W-S wird durch Abschreckungsexperimente in evakuierten Quarzglasampullen sowie durch Differential-Thermoanalyse untersucht, die Phasengleichgewichtsbeziehungen sind in einem isothermen Digramm T<743 °C veranschaulicht. Unterhalb 743±2 °C liegt der Stabilitätsbereich des Pyrits, FeS₂, welcher mit Tungstenit, WS₂, koexistiert. Konodenscharen erstrecken sich ferner von WS₂ zu Pyrrhotin und zwar über einen weiten Bereich der Fe_1-xS-Mischkristallreihe. Von FeS, oder annähernd stöchiometrischem FeS verlaufen Konoden zum metallischen Wolfram und zu den intermetallischen Phasen Fe₂W und Fe₃W₂. Eine ternäre Phase wurde nicht gefunden. Experimente im ternären sowie im quaternären System Fe-W-O-S demonstrieren, daß WS₂ weder mit metallischem Eisen noch mit Eisenoxiden stabil ist. Molybdän und Wolfram zeichnen sich durch unterschiedliche Affinität zu Schwefel aus, und daraus resultierende Schlußfolgerungen werden in bezug auf natürliche Mineralvergesellschaftungen diskutiert. Die in der einschlägigen Literatur gemachten Angaben über die Schwefelfugazität von Fe, Mo und W werden kritisch untersucht. Dominierende Unterschiede hinsichtlich der Phasengleichgewichtsbeziehungen des Fe-W-S-Diagrammes zu anderen Fe-beinhaltenden Sulfidsystemen, wie Fe-Mo-S, Fe-Sn-S und Fe-Bi-S, werden aufgezeigt.

     

Biomarker distributions as indicators for the depositional environment of lacustrine sediments in the Valjevo-Mionica basin (Serbia)

In this study, the molecular composition and biomarker distribution of lacustrine sediments from Val-1 drillhole in the central zone of the western part of the Valjevo-Mionica basin were investigated at depth interval of 0–400 m. Former investigations have shown that the core material can be separated into six depth intervals based on bulk geochemical, mineralogical and sedimentological characteristics. Concerning the quality of organic matter, presence of specific minerals, and high salinity and anoxicity, or alkalinity, three zones are of highest interest, defined at depth intervals of 15–75 m (A), 75–200 m (B) and 360–400 m (F). The first aim of the study was to identify which biomarkers characterize these specific intervals. The second aim, addressing the transitions zones of these intervals, was to extend the changes in the characteristics of the organic substance, to reflect the changes of conditions in the depositional environment as well as to define biomarker parameters which are the most sensitive sedimentological indicators.The sediments from the hypersaline anoxic and alkaline environment show high contribution of algal precursor biomass, what is in accordance with the good quality of organic substances in the sediments from these zones. High squalane content and low content of regular isoprenoid C₂₅ are typical for hypersaline anoxic environment, whereas sediments from alkaline environment have high regular isoprenoid C₂₅ content.Transition to specific sedimentation zones is characterized by change in total organic matter content, and of both free and pyrolysis-derived, and change in hydrogen index value. In the biomarker distributions, more significant changes were detected in distributions of n-alkanes and isoprenoids, compared to polycyclic alkanes. The most intensive changes in alkane distribution are reflected in changes in n-C₁₇ content compared to n-C₂₇, and phytane compared to n-C₁₈. In addition, significant sensitivity was seen in ratios between squalane and n-alkane C₂₆ (hypersaline depositional environment), or isoprenoid C₂₅ and n-alkane C₂₂ for high alkalinity environment.This study showed that Sq/n-C₂₆ ratio can be used to assess the quality of organic substance in immature lacustrine sediments.     

Chemical Dynamics and Evaluation of Biogeochemical Processes in Alpine River Kamniška Bistrica, North Slovenia

Biogeochemical processes were investigated in alpine river—Kamni?ka Bistrica River (North Slovenia), which represents an ideal natural laboratory for studying anthropogenic impacts in catchments with high weathering capacity. The Kamni?ka Bistrica River water chemistry is dominated by HCO₃ ^?, Ca²⁺ and Mg²⁺, and Ca²⁺/Mg²⁺ molar ratios indicate that calcite weathering is the major source of solutes to the river system. The Kamni?ka Bistrica River and its tributaries are oversaturated with respect to calcite and dolomite. pCO₂ concentrations were on average up to 25 times over atmospheric values. δ¹³C_DIC values ranged from ?12.7 to ?2.7 ‰, controlled by biogeochemical processes in the catchment and within the stream; carbonate dissolution is the most important biogeochemical process affecting carbon isotopes in the upstream portions of the catchment, while carbonate dissolution and organic matter degradation control carbon isotope signatures downstream. Contributions of DIC from various biogeochemical processes were determined using steady state equations for different sampling seasons at the mouth of the Kamni?ka Bistrica River; results indicate that: (1) 1.9–2.2 % of DIC came from exchange with atmospheric CO₂, (2) 0–27.5 % of DIC came from degradation of organic matter, (3) 25.4–41.5 % of DIC came from dissolution of carbonates and (4) 33–85 % of DIC came from tributaries. δ¹⁵N values of nitrate ranged from ?5.2 ‰ at the headwater spring to 9.8 ‰ in the lower reaches. Higher δ¹⁵N values in the lower reaches of the river suggest anthropogenic pollution from agricultural activity. Based on seasonal and longitudinal changes of chemical and isotopic indicators of carbon and nitrogen in Kamni?ka Bistrica River, it can be concluded that seasonal changes are observed (higher concentrations are detected at low discharge conditions) and it turns from pristine alpine river to anthropogenic influenced river in central flow.     

Anthropogenic influence on trace element geochemistry of healing mud (peloid) from Makirina Cove (Croatia)

Due to their balneotherapeutic features, the organic-rich sediments in Makirina Cove are an important source of healing mud. An environmental geochemistry approach using normalization techniques was applied to evaluate the anthropogenic contribution of trace metals to sediments used as healing mud. Sediment geochemistry was found to be associated with land-use change and storm events, as well as with proximity of a road with heavy traffic in the summer months. Local valley topography preferentially channels lithogenic and pollutant transport to the cove. Concentrations and distribution of trace metals indicate lithogenic (Ni, Cr, Co) and anthropogenic (Pb, Cu, Zn and Se) contributions to the sediments. The calculation of enrichment factors indicates a moderate (EFs between 2–3.5) input of anthropogenic Cu and Pb in surficial sediments to a depth of 10 cm. Patients using the Makirina Cove sediments as healing mud could be to some extent exposed to enhanced uptake of metals from anthropogenic sources via dermal contact.