The mafic-ultramafic complex near Finero (Ivrea-Verbano Zone), I. Chemistry of MORB-like magmas

Geochemical data are presented for the meta-igneous, mafic-ultramafic complex near Finero. This complex is in contact with a phlogopite-bearing mantle peridotite and is subdivided into the Internal Gabbro unit, the Amphibole Peridotite unit, and the External Gabbro unit. The Internal Gabbro and the Amphibole Peridotite units consist of coarse-grained, chemically heterogeneous cumulates, whereas the External Gabbro unit is generally massive, chemically more uniform and approximately representative of the residual melt with MgO contents between 6.6 and 9.1% and Mg numbers between 38 and 58. Both whole-rock and mineral contents of Ni and Cr are significantly higher (at similar Mg numbers) in the Amphibole Peridotite unit than in the Internal Gabbro unit. The most straightforward interpretation of this is that the Amphibole Peridotite unit accumulated after the influx of fresh mafic (or ultramafic) magma into the magma chamber. Major-element chemical trends are continuous from the Amphibole Peridotite unit to the External Gabbro unit and are consistent with closed-system fractionation with no further addition of magma or contamination by wall or roof rock assimilation. In the External Gabbro unit, total FeO and TiO₂ contents are strongly correlated with each other (and with P₂O₅ and Zr) and reach values as high as 19 and 4%, respectively, indicating an advanced degree of crystal fractionation along a tholeftic trend. The External Gabbro samples have generally smooth normalized trace element patterns, which are consistent with being representative of a liquid composition. The residual nature of the External Gabbro magma is also indicated by negative Eu and Sr anomalies, clear evidence for prior feldspar fractionation. REE patterns are otherwise indistinguishable from N-type MORB, but Th and U are significantly more depleted than in MORB. This Th and U depletion is similar to that found in olivine basalts and picrites on Iceland and Hawaii; its origin is not well understood. No evidence is seen for any assimilation of crystal material, in sharp contrast with the situation of the igneous complex in Val Sesia near Balmuccia, where the magma composition is dominated by assimilation of crust. We suggest that the heat provided by at most two injections of magma near Finero was insufficient to induce crystal anatexis, in contrast with the excess heat supplied by multiple magma injections at Balmuccia.     

Chemical fractionations in meteorites—X. Ureilites

Four ureilites (Dyalpur, Goalpara, Haverö, and Novo Urei) were analyzed by radiochemical neutron activation analysis for Ag, Au, Bi, Br, Cd, Cs, Ge, In, Ir, Ni, Rb, Re, Sb, Se, Te, Tl, and U. An attempt has been made to resolve the data into contributions from the parent ultramafic rock and the injected, carbon- and gas-rich vein material. Interelement correlations, supported by analyses of separated vein material (WANKE et al, 1972), suggest that the vein material is enriched about 10-fold in refractory Ir and Re over moderately volatile Ni and Au, and is low in volatiles except Ge, C, and noble gases. It appears to be a refractory-rich nebular condensate that precipitated carbon by surface catalytic reactions at ˜500K and trapped noble gases but few other volatiles. The closest known analogue is a Cr- and C-rich fraction from the Allende meteorite, highly enriched in heavy noble gases and noble metals. By analogy with Allende, the gas-bearing phase in ureilites may have been an Fe, Cr-sulfide.

The ultramafic rock contains siderophiles and chalcophiles (Ni, Au, Ge, S, Se) at ˜0.05 of Cl chondrite level, and highly volatile elements (Rb, Cs, Bi, Tl, Br, Te, In, Cd) at ˜0.01 Cl level. It probably represents the residue from partial melting of a C3V-like chondrite body, under conditions where phase separation was incomplete so that some liquid was retained. The vein material was injected into this rock at some later time.     

Magma mixing: the Marsco suite,Isle of Skye,Scotland

Magma mixing has been proposed as a major mechanism for the origin of a wide variety of rock suites. In mid-ocean basalts there are few obstacles to mixing because of the similarities in chemical and physical properties of the proposed end-members. However, in calc-alkaline rocks the proposed end-members have disparate properties and these present obstacles to mixing.The Marsco suite is ideal to evaluate the process of magma mixing because it is considered to be a classic example of magma mixing of diverse magma types and because compositionally diverse, coexisting liquids were present throughout the area.The results of this study are that the chemical data for the Marsco suite fit a mixing model remarkably well and that the mixing did not take place at the present level of exposure. The Marsco mixed suite is similar to the experiments of Kouchi and Sunagawa (1982, 1983) in which mixing was produced by forced convection. Based on the Marsco suite, a similar occurrence in Ardnamurchan, and the experimental data, we conclude that mixing was dominated by mechanical mixing and this mechanical mixing was efficient enough to allow diffusional processes to homogenize the liquids.It is postulated that injection of mafic magma into the base of a silicic magma system leads to mixing and mobilization of the system. The mechanical interaction that produces the mixing also leads to disruption of the system. Liquids involved with the mixing process at depth are mobilized and coexist at shallower levels.     

Moisture sorption behaviour of salt mixtures in porous stone

Moisture in stone material is the key factor for all stone deterioration processes and also in weathering of cultural heritage. With additional presence of salts in the material the situation gets even more critical. While the properties of pure salts with moisture are well known, knowledge about the interaction of salt mixtures with moisture is still poor. In different approaches the reactions of salt-contaminated stone material on changing moisture were tested in the laboratory. Experiments with different solutions in the Na-Mg-SO₄-NO₃-H₂O system revealed interesting new results on the moisture behaviour of salt-contaminated samples. Theoretical considerations and computer simulations are helpful to interpret the data obtained, but are not yet sufficient to explain the real processes acting on site at the monuments. More encouraging to this fact are complementary studies on visible efflorescences in the same salt system. It is shown how by experimental approaches the understanding on salt-induced stone deterioration is strongly complemented.     

Paleomagnetic dating of Alleghanian orogenesis and mineralisation in the Mascot–Jefferson City zinc district of East Tennessee, USA

The Mascot–Jefferson City (M-JC) Mississippi Valley-type (MVT) deposits are in the Valley and Ridge province of the Appalachian orogen in East Tennessee. They have been a major source of zinc for the USA but their age is uncertain and thus their genesis controversial. About 10 specimens from each of 37 sites have been analysed paleomagnetically using alternating field and thermal step demagnetisation methods and saturation isothermal remanence methods. The sites sample limestones, dolostones, breccia clasts and sphalerite–dolomite MVT mineralisation from mines in the Lower Ordovician Kingsport and Mascot formations of the Knox Group. The characteristic remanent magnetisation (ChRM) is carried by magnetite in the limestones, by both magnetite and pyrrhotite in the dolostones and by pyrrhotite preferentially to magnetite in the mineralisation. Mineralized sites have a more intense ChRM than non-mineralised, indicating that the mineralising and magnetisation event are coeval. Paleomagnetic breccia tests on clasts at the three sites are negative, indicating that their ChRM is post-depositional remagnetisation, and a paleomagnetic fold test is negative, indicating that the ChRM is a remagnetisation, and a post-dates peak Alleghanian deformation. The unit mean ChRM direction for the: (a) limestones gives a paleopole at 129°E, 12°N (d_p=18°, d_m=26°, N=3), indicating diagenesis formed a secondary chemical remanent magnetisation during the Late Ordovician–Early Silurian; (b) dolomitic limestones and dolostone host rocks gives a paleopole at 125.3°E, 31.9°N (d_p=5.3°, d_m=9.4°, N=7), recording regional dolomitisation at 334±14 Ma (1σ); and (c) MVT mineralisation gives a paleopole at 128.7°E, 34.0°N (d_p=2.4°, d_m=4.4°, N=25), showing that it acquired its primary chemical remanence at 316±8 Ma (1σ). The mineralisation is interpreted to have formed from hydrothermal fluid flow, either gravity or tectonically driven, after peak Alleghanian deformation in eastern Tennessee with regional dolomitisation of the host rocks occurring as part of a continuum during the 20 Ma prior to and during peak deformation.     

Prehistoric gold markers and environmental change: A two‐age system for standing stones in western Ireland

The Murrisk Peninsula in southwest County Mayo is a major target for gold exploration in Ireland. The most productive areas include the Cregganbaun Shear Zone and Cregganbaun Quartzite Belt on Croagh Patrick, both geologically related to Iapetus closure, and gold is concentrated in alluvial deposits of river systems draining these areas. A comparison of gold occurrences with the location of prehistoric stone monuments reveals that simple standing‐stone monuments, though isolated from other monument types, correlate with alluvial gold. South of the Murrisk Peninsula in Connemara, isolated standing stones are associated with a wide range of mineral resources and with other monuments. Dating of the stones relative to blanket‐bog expansion and coastal landform changes indicates that standing stones were raised as markers of gold placer deposits before a climatic deterioration at 1200 B.C. Late Bronze Age monuments with a ceremonial purpose are more complex and include stone alignments. © 2006 Wiley Periodicals, Inc.     

The oxidation states of cobalt and selected metals in Pacific ferromanganese nodules

A study of the oxidation states of metals in selected Pacific ferromanganese nodules by x-ray photoelectron spectroscopy (XPS) indicates the presence of Co(III), Pb(II), Pb(IV), Fe(III) and Ti(IV). These findings are based on measurements of core electron binding energies and an evaluation of the core electron shake-up satellite features.     

High resolution facies record on late Holocene flood plain sediments from lower reaches of Narmada Valley,Western India

A high resolution quantitative granulometric record for site Uchediya [21°43′2.22″ N, 73° 6′26.22″ E; 10 m a. s. l.] gives understanding towards accretion history of the late Holocene flood plain in the lower reaches of Narmada River. Two sediment facies (sandy and muddy) and seven subfacies (sandy subfacies: St_MS+FS+CS, Sm_FS+MS, Sl_FS+VFS, and St_{MS + CS}; muddy subfacies: Fm_SILT+VFS+FS, Fm_SILT+VFS (O) and Fm_SILT+VFS (T)) are identified based on cluster analysis supplemented with sedimentary structures observed in field and other laboratory data. Changes in hydrodynamics are further deduced based on various sedimentological parameters and their ratios leading to arrive at a depositional model.     

Magnetohydrodynamic flow of a non-Newtonian fluid past a porous plate

This article studies the laminar flow of an electrically conducting non-Newtonian fluid (Rivlin-Encksen type) past an infinite porous flat plate to a step function change in suction velocity in the presence of a transverse magnetic field. The Laplace transform technique has been employed to solve the basic differential equations. The solutions of the velocity profile and skin-friction are obtained and the effects of the visco-elastic parameter, the magnetic field and the time parameter on the fluid flow have been studied in several tables.     

Solar rotation velocity as determined from sunspot drawings of J. Hevelius in the 17th century

Using two original copies of Hevelius' Selenographia and reducing spot positions with two different methods, we found that the solar angular rotation velocity at the beginning of the Maunder minimum was about the same as today. The gradient of the differential rotation was slightly steeper than given in modern reductions, but not significantly different. These findings are in contradiction to those published by Eddy et al. (1976).