Cyclic variations in the differential rotation of the solar corona

The rotation of the solar corona is analyzed using the original database on the brightness of the FeXIV 530.3 nm coronal green line covering six recent activity cycles. The rate of the differential rotation of the corona depends on the cycle phase. In decay phases, there are only small differences in the rotation, which are similar to that of a rigid body. The differences are more significant (though less pronounced than in the photosphere) during rise phases, just before maxima, and sometimes at maxima. The total rate of the coronal rotation is represented as a superposition of two, i.e., fast and slow modes. The synodic period of the fast mode is approximately 27 days at the equator and varies slightly with time. This mode displays weak differences in rotation and is most pronounced in the middle of decay phases. The slow mode is manifested only at high latitudes during the rise phases of activity, and displays a mean period of 31 days. The relative contribution of each mode to the total rotational rate is determined as a function of time and heliographic latitude. These results indicate that the structure of the velocity field in the convective zone must also vary with time. This conclusion can be verified by helioseismology measurements in the near future.     

Quantification of karst aquifer discharge components during storm events through end-member mixing analysis using natural chemistry and stable isotopes as tracers

Karst aquifer components that contribute to the discharge of a water supply well in the Classical Karst (Kras) region (Italy/Slovenia) were quantitatively estimated during storm events. Results show that water released from storage within the epikarst may comprise as much as two-thirds of conduit flow in a karst aquifer following rainfall. Principal components analysis (PCA) and end-member mixing analysis (EMMA) were performed using major ion chemistry and the stable isotopes of water (δ¹⁸O, δ²H) and of dissolved inorganic carbon (δ¹³C_DIC) to estimate mixing proportions among three sources: (1) allogenic river recharge, (2) autogenic recharge, and (3) an anthropogenic component stored within the epikarst. The sinking river most influences the chemical composition of the water-supply well under low-flow conditions; however, this proportion changes rapidly during recharge events. Autogenic recharge water, released from shallow storage in the epikarst, displaces the river water and is observed at the well within hours after the onset of precipitation. The autogenic recharge end member is the second largest component of the well chemistry, and its contribution increases with higher flow. An anthropogenic component derived from epikarstic storage also impacts the well under conditions of elevated hydraulic head, accounting for the majority of the chemical response at the well during the wettest conditions.     

Redbed-type gold mineralisation, Kupferschiefer, south-west Poland

A new type of gold mineralisation containing minor amounts of platinum and palladium has been found proximal to the secondary redox interface located below the Cu-Ag Kupferschiefer orebody of the Polkowice-Sieroszowice mine in the south-western part of the Lubin-Sieroszowice district, Poland. This deposit can be classified as redbed-type gold. Our study shows that gold, platinum and palladium occur in secondary red-coloured sections of the basal Zechstein sedimentary rocks and in the uppermost Weissliegendes sandstone. Noble metal mineralisation occurs within an average interval of 0.22 m, which lies directly below the copper ores. The average grade of the horizon is 2.25 ppm Au, 0.138 ppm Pt and 0.082 ppm Pd with a metal content of several tens of tonnes of gold. A transition zone has been recognised between the gold-bearing horizon and the copper deposit. This transition zone is characterised by the presence of low grades of copper (<0.2 wt%) and elevated gold contents (>0.5 ppm). Native gold accompanied by electrum, mercury-bearing gold, haematite, covellite, chalcocite, bornite and chalcopyrite has been identified in the gold-bearing horizon. In some sections, Pd-arsenides, tetra-auricupride, Co-arsenides, clausthalite, tennantite, digenite, yarrowite, spionkopite and galena have also been noted.     

Rates of Deglaciation during the Last Glaciation and Holocene in the Cordillera Vilcanota-Quelccaya Ice Cap Region, Southeastern Perú

Moraine chronology is combined with digital topography to model deglacial rates of paleoglacier volumes in both the Huancané Valley on the west side of the Quelccaya Ice Cap and the Upismayo Valley on the northwest side of the Cordillera Vilcanota. The fastest rates of deglaciation (39×10⁻⁵ to 114×10⁻⁵ km³ yr⁻¹ and 112×10⁻⁵ to 247×10⁻⁵ km³ yr⁻¹ for each valley, respectively) were calculated for the most recent paleoglaciers, corresponding to the last few centuries. These results are consistent with observations in the Venezuelan Andes showing high rates of deglaciation since the Little Ice Age. These rates also fall within the range of 20th century rates of deglaciation measured on the Quelccaya Ice Cap (29×10⁻⁵ to 220×10⁻⁵ km³ yr⁻¹, Brecher and Thompson, 1993; Thompson, 2000). These results imply that rates of deglaciation may fluctuate significantly over time and that high rates of deglaciation may not be exclusive to the late 20th century. Equilibrium line altitude (ELA) depressions for the ice volumes of the last glaciation modeled here were computed as 230 m for the Quelccaya Ice Cap and 170 m for the Cordillera Vilcanota. Maximum ELA depressions are lower than previously published: <500 m for the Cordillera Vilcanota and <400 m for the Quelccaya Ice Cap. These lower values could imply a topographic control over paleoglacier extent.     

Analyzing CO2 emissions mitigation by technology improvement in Central and Eastern Europe

As a legacy of the centrally planned economy, the economies in transition of Central and Eastern Europe (CEE) have a unique potential to reduce their greenhouse gas emissions through the improvement in their high energy intensities. Since much of this `low-hanging fruit' in energy-efficiency improvements can be highly cost-effective, many developed countries facing difficulties in meeting their greenhouse gas (GHG) emission targets domestically are eager to find such opportunities in the CEE region. Therefore, studies analysing the potentials and costs of carbon dioxide reduction through technology improvement in the region have come into the limelight. While there are a few excellent studies in the region aimed at analysing climate change abatement potentials, they all embark on different assumptions, methodologies and boundary conditions. It is hence difficult, if not impossible, to compare and analyse the results of these studies across different authors, countries or time horizons. Consequently, the purpose of this paper is to place four leading studies on GHG mitigation through technology improvement from the CEE region into an internationally comparable framework. Four studies were selected from three countries, Poland, Hungary and Estonia, which are all the results of major national and international efforts to assess costs and potentials of GHG reduction. The paper places their assumptions, methods and final results into a framework which enables policy-makers and project designers to compare these across geographical and technological boundaries. Since other studies from around the globe have been analysed in this framework in the literature, this paper provides a vehicle for the findings of these four studies to be compared to others worldwide. In addition, the paper highlights a few areas where similar studies to be completed in the future in the region may be enhanced by incorporating features used in GHG mitigation research in other parts of the world. This revised version was published online in July 2006 with corrections to the Cover Date.     

Pressure effect on Ti- or P-rich accessory mineral saturation in evolved granitic melts with differing K2O/Na2O ratios

The solubility of Ti- and P-rich accessory minerals has been examined as a function of pressure and K₂O/Na₂O ratio in two series of highly evolved silicate systems. These systems correspond to (a) alkaline, varying from alkaline to peralkaline with increasing K₂O/Na₂O ratio; and (b) strongly metaluminous (essentially trondhjemitic at the lowest K₂O/Na₂O ratio) and remaining metaluminous with increasing K₂O/Na₂O ratio (to 3). The experiments were conducted at a fixed temperature of 1000 °C, with water contents varying from 5 wt.% at low pressure (0.5 GPa), increasing through 5–10 wt.% at 1.5–2.5 GPa to 10 wt.% at 3.5 GPa. Pressure was extended outside the normal crustal range, so that the results may also be applied to derivation of hydrous silicic melts from subducted oceanic crust.

For the alkaline composition series, the TiO₂ content of the melt at Ti-rich mineral saturation decreases with increasing pressure but is unchanged with increasing K content (at fixed pressure). The P₂O₅ content of the alkaline melts at apatite saturation increases with increased pressure at 3.5 GPa only, but decreases with increasing K content (and peralkalinity). For the metaluminous composition series (termed as “trondhjemite-based series” (T series)), the TiO₂ content of the melt at Ti-rich mineral saturation decreases with increasing pressure and with increasing K content (at fixed pressure). The P₂O₅ content of the T series melts at apatite saturation is unchanged with increasing pressure, but decreases with increasing K content. The contrasting results for P and Ti saturation levels, as a function of pressure in both compositions, point to contrasting behaviour of Ti and P in the structure of evolved silicate melts. Ti content at Ti-rich mineral saturation is lower in the alkaline compared with the T series at 0.5 GPa, but is similar at higher pressures, whereas P content at apatite saturation is lower in the T series at all pressures studied. The results have application to A-type granite suites that are alkaline to peralkaline, and to I-type metaluminous suites that frequently exhibit differing K₂O/Na₂O ratios from one suite to another.     

Petrology and geochemistry of orthoamphibolites from the Variscan metamorphic sequences of the South Tisia in Croatia – an overview with geodynamic implications

In the southern Pannonian Basin, the Variscan Barrovian- and overprinted Abukuma-type progressive metamorphic sequences of the South Tisia in Slavonian Mts. (SM) and Mt. Moslava)ka Gora (MG) are interlayered with orthoamphibolites. These sequences represent part of a disrupted Variscan belt that extends southeastwards of the Bohemian Massif through the Carpathians to the Caucasus. Orthoamphibolites contain hornblende (Mg-hornblende, tschermakite, pargasite, and edenite), plagioclase An_48-98 (MG) and An_26-35 (SM), biotite, grossular (MG) and almandine (SM) enriched garnet, diopside (MG), with accessory ilmenite, titanite, and clinozoisite. Based on major and trace element analyses and CIPW norms, these orthoamphibolites, which originally were olivine tholeiites to slightly alkalic basalts, can be correlated with tholeiites of consuming plate margins. '¹⁸O of orthoamphibolites varies from 5.8 to 7.1‰, the measured ⁸⁷Sr/⁸⁶Sr ratio from 0.70435 to 0.70665, which indicates slight continental crust contamination, and the calculated ratio from 0.70262 to 0.70535, indicating an upper mantle origin of the original basaltic melts. For associated penecontemporaneous I-type granitoids, the calculated initial ⁸⁷Sr/⁸⁶Sr ratio also have upper mantle values ranging between 0.70293 and 0.70368. Geochemical data for orthoamphibolites and the associated penecontemporaneous I-type granites, and the occurrence of alpine-type ultramafic bodies within the Barrovian sequence, indicate that they have many features in common with orogenic associations related to recent subduction-related settings. Some characteristic element ratios suggest back-arc basin environments and the Ce/K vs. Ce diagram suggests a pargasite-lherzolite source. Its partial melting gave primitive basaltic melts of olivine tholeiite to slight alkalic affinities that produced at first differentiated mafic rocks by olivine fractionation (future orthoamphibolites) and, afterwards, a strongly differentiated suite of I-type granitoids by amphibole fractionation. Magma emplacement and subsequent AFC processes took place in subduction environments preceding the main Variscan deformational metamorphic event during which orthoamphibolites were generated. This interpretation is compatible with geodynamic modeling of this part of the Paleotethys.