Sedimentation on the Ionian active margin (Hellenic arc) — Provenance of sediments and mechanisms of deposition

Lithological, sedimentological, mineralogical and faunal analyses of twenty cores from the western Peloponnesus margin and adjacent Matapan Trench permit the origin of the sediments and the processes of sedimentation to be defined in some detail.Except for the ash layers derived from the Ischian Province, the major part of the sediment is local in origin (Peloponnesus). Analyses of heavy, light and clay minerals enable three main provinces to be distinguished. Each of these provinces includes one or more slope basins and a portion of trench, without lateral connection between them and mixing of inputs.The diversity and complexity of sedimentary structures, the granulometric characters, the mixed fauna (molluscs and ostracods) and the variability of rates of sedimentation all testify to the prevalence of reworking phenomena and gravitative processes.These data confirm and elaborate on the model of sedimentation deduced from seismic studies in which sediments are successively trapped, released by the slope basins and transferred via channels and canyons towards the underlying trench basins. This “cascade feeding” appears characteristics of this subductive sedimentary environment.     

Thermodynamic controls on element partitioning between titanomagnetite and andesitic–dacitic silicate melts

Titanomagnetite–melt partitioning of Mg, Mn, Al, Ti, Sc, V, Co, Ni, Cu, Zn, Ga, Zr, Nb, Mo, Hf and Ta was investigated experimentally as a function of oxygen fugacity (fO₂) and temperature (T) in an andesitic–dacitic bulk-chemical compositional range. In these bulk systems, at constant T, there are strong increases in the titanomagnetite–melt partitioning of the divalent cations (Mg²⁺, Mn²⁺, Co²⁺, Ni²⁺, Zn²⁺) and Cu²⁺/Cu⁺ with increasing fO₂ between 0.2 and 3.7 log units above the fayalite–magnetite–quartz buffer. This is attributed to a coupling between magnetite crystallisation and melt composition. Although melt structure has been invoked to explain the patterns of mineral–melt partitioning of divalent cations, a more rigorous justification of magnetite–melt partitioning can be derived from thermodynamic principles, which accounts for much of the supposed influence ascribed to melt structure. The presence of magnetite-rich spinel in equilibrium with melt over a range of fO₂ implies a reciprocal relationship between a(Fe²⁺O) and a(Fe³⁺O_1.5) in the melt. We show that this relationship accounts for the observed dependence of titanomagnetite–melt partitioning of divalent cations with fO₂ in magnetite-rich spinel. As a result of this, titanomagnetite–melt partitioning of divalent cations is indirectly sensitive to changes in fO₂ in silicic, but less so in mafic bulk systems.     

FORWARD MODELING IN THE FREQUENCY-SPACE DOMAIN*

Forward modeling of zero-offset data is performed in the frequency-space domain using a one-way extrapolation equation. The use of the frequency domain offers several advantages over conventional time domain methods. The greatest advantage of the frequency domain is that all time derivatives are evaluated exactly by a simple multiplication. Synthetic zero-offset sections are computed with a high degree of accuracy for arbitrary velocity and reflectivity structures. Examples are shown for realistic complicated models and compared with results from physical modeling.     

Age and isotopic studies of some Pan-African granites from North-Central Nigeria

Twenty-nine Rb-Sr whole-rock isotopic analyses and three U-Pb zircon analyses on foliated granites and largely unfoliated charnockitic rocks indicate that the central part of the Pan-African belt in west Africa was characterised by intense orogenic plutonism. These data and Rb-Sr analyses on muscovite books from late cross-cutting pegmatites indicate that the peak of magmatic activity occurred 610 ± 10 m.y. ago.Initial ⁸⁷Sr/⁸⁶Sr ratios for the granitic and charnockitic rocks are in the range 0.7065–0.7125, and indicate a significantly older crustal component in the magmas.     

Tropospheric Ozone in a Global-Scale Three-Dimensional Lagrangian Model and Its Response to NOX Emission Controls

A three-dimensional Lagrangian tropospheric chemistry modelis used toinvestigate the impact of human activities on the tropospheric distributionofozone and hydroxyl radicals. The model describes the behaviour of 50 speciesincluding methane, carbon monoxide, oxides of nitrogen, sulphur dioxide andnineorganic compounds emitted from human activities and a range of other sources.Thechemical mechanism involves about 100 chemical reactions of which 16 arephotochemical reactions whose diurnal dependence is treated in full. The modelutilises a five minute chemistry time step and a three hour advection timestepfor the 50,000 air parcels. Meteorological data for the winds, temperatures,clouds and so on are taken from the UK Meteorological Office global model for1994 onwards. The impacts of a 50% reduction in European NO_Xemissions onglobal ozone concentrations are assessed. Surface ozoneconcentrations decrease in summertime and rise in wintertime, but to differentextents.     

A NEW APPROACH TO THE INVERSION OF SEISMIC DATA*

A new inversion method for seismic reflection data is based on impedance concepts and uses transformations to reduce the essentially non-linear problem to a linear eigenvalue formulation without approximation. A set of reflection data has been inverted using this method. The characteristic impedances of the layers so determined are compared with log data from a reference borehole.     

Mineralogical, chemical, and crystallographic properties of supergene jarosite-group minerals from the Xitieshan Pb-Zn sulfide deposit, northern Tibetan Plateau, China

Supergene jarosite-group minerals are widespread in weathering profiles overlying Pb-Zn sulfide ores at Xitieshan, northern Tibetan Plateau, China. They consist predominantly of K-deficient natrojarosite, with lesser amounts of K-rich natrojarosite and plumbojarosite. Electron microprobe (EMP) analyses, scanning electron microcopy (SEM) investigation, and X-ray mapping reveal that the jarosite-group minerals are characterized by spectacular oscillatory zoning composed of alternating growth bands of K-deficient and K-bearing natrojarosite (K₂O >1 wt.%). Plumbojarosite, whenever present, occurs as an overgrowth in the outermost bands, and its composition can be best represented by K_0.29Na_0.19Pb_0.31Fe_2.66Al_0.22(SO₄)_1.65(PO₄)_0.31(AsO₄)_0.04(OH)_7.37. The substitution of monovalent for divalent cations at the A site of plumbojarosite is charge balanced by the substitution of five-valent for six-valent anions in XO₄ at the X site. Thermogravimetric analysis (TGA) of representative samples reveal mass losses of 11.46 wt.% at 446.6 °C and 21.42 wt.% at 683.4 °C due to dehydroxylation and desulfidation, respectively. TGA data also indicate that the natrojarosite structure collapses at 446.6 °C, resulting in the formation of NaFe(SO₄)₂ and minor hematite. The decomposition products of NaFe(SO₄)₂ are hematite and Na₂SO₄. Powder X-ray diffraction (XRD) analyses show that the jarosite-group minerals have mean unit-cell parameters of a?=?7.315 Å and c?=?016.598 Å. XRD and EMP data support the view that substitutions of Na for K in the A site and full Fe occupancy in the B site can considerably decrease the unit-cell parameter c, but only slightly increase a. The results from this study suggest that the observed oscillatory zoning of jarosite-group minerals at Xitieshan resulted mainly from substitutions of K for Na at the A site and P for S at the X site.     

Subpollen Particles as Atmospheric Cloud Condensation Nuclei

Izvestiya, Atmospheric and Oceanic Physics - Bioparticles constitute a significant fraction of atmospheric aerosol. Their size range varies from nanometers (macromolecules) to hundreds of...     

The effect of composition,temperature and pressure on the stability of the 1Tc and 2M polytypes of sapphirine

Microprobe analyses and structural characterisation by means of transmission electron microscopy and powder X-ray diffraction are presented for a suite of natural and synthetic sapphirines. Most sapphirines appear to consist of intergrowths of the common 2M polytype with minor amounts of the 1Tc phase, although the converse situation is found in some cases. Attempts to correlate the structural state of the mineral with other factors reveal that: (i) There is no strong relationship between mean tetrahedral cation radius or mean octahedral cation radius and the preferred polytype. The Tschermak substitution M²⁺M⁴⁺-M³⁺M³⁺ does not appreciably influence the 1Tc-2M equilibrium, (ii) However, the total content and mean oxidation state of iron in sapphirine are important in this respect. Fe²⁺ stabilises the 2M phase, whereas Fe³⁺ stabilises the 1Tc phase. (iii) P-T estimates for the host rocks, and estimates for the conditions of sapphirine crystallisation, where obtainable, suggest that the 1Tc phase is stable at lower T and higher P than the 2M phase. Some quantitative constraints are inferred.