Intrusive processes at ocean ridges: Evidence from the sheeted dyke complex of Masirah, Oman

Masirah Island largely consists of a late Mesozoic ophiolite which includes extensive areas of near-vertical, ENE—WSW striking, sheeted dykes. Previously the possibility has been suggested of a correlation between the similarly-aged ophiolites of Masirah and the Semail Complex of the Oman Mts. However, the Masirah ENE–WSW trend contrasts with N—S dyke trends from the Wadi Jizi area of the Semail, possibly suggesting two unrelated spreading centres. The dykes pass up into a pillow lava—minor sediment sequence, down into both layered and unlayered gabbros and are bounded to the west by a major N—S mélange zone which may have originated as a ridge transform fault. Age relations of the dykes and the gabbros are complex: the dykes contain a variable proportion of gabbro screens representing earlier crystallization, but they are also intruded by several small gabbro bodies which are themselves cut by still later dykes. The lava and dyke—gabbro screen sequence shows evidence of metamorphism from zeolite to low amphibolite grade. This metamorphism was caused by ridge hydrothermal activity which appears to have been effective approximately to the lower levels of the dykes. The rapid passage from low-amphibolite dykes to fresh gabbro suggests lithological control of the metamorphism. A combination of structural, geochemical and mineral phase studies may indicate generation in a slow spreading ridge environment and near-ridge metamorphism caused by a geothermal gradient of approximately 200°C/km.     

Schorlomite: a discussion of the crystal chemistry, formula, and inter-species boundaries

Examination of schorlomite from ijolite at Magnet Cove (USA) and silicocarbonatite at Afrikanda (Russia), using electron-microprobe and hydrogen analyses, X-ray diffraction and Mössbauer spectroscopy, shows the complexity of substitution mechanisms operating in Ti-rich garnets. These substitutions involve incorporation of Na in the eightfold-coordinated X site, Fe²⁺ and Mg in the octahedrally coordinated Y site, and Fe³⁺, Al and Fe²⁺ in the tetrahedrally coordinated Z site. Substitutions Ti⁴⁺Fe³⁺Fe³⁺_–1Si_–1 and Ti⁴⁺Al³⁺Fe³⁺_–1Si_–1 are of major significance to the crystal chemistry of schorlomite, whereas Fe²⁺ enters the Z site in relatively minor quantities (<3% Fe). There is no evidence (either structural or indirect, such as discrepancies between the measured and calculated Fe²⁺ contents) for the presence of ^[6]Ti³⁺ or ^[4]Ti⁴⁺ in schorlomite. The simplified general formula of schorlomite can be written as Ca₃Ti⁴⁺₂[Si_3-x(Fe³⁺,Al,Fe²⁺)_xO₁₂], keeping in mind that the notion of end-member composition is inapplicable to this mineral. In the published analyses of schorlomite with low to moderate Zr contents, x ranges from 0.6 to 1.0, i.e. Ti⁴⁺ in the Y site is <2 and accompanied by appreciable amounts of lower-charged cations (in particular, Fe³⁺, Fe²⁺ and Mg). For classification purposes, the mole percentage of schorlomite can be determined as the amount of ^[6]Ti⁴⁺, balanced by substitutions in the Z site, relative to the total occupancy in the Y site: (^[6]Ti⁴⁺–^[6]Fe²⁺–^[6]Mg²⁺– ^[8]Na⁺)/2. In addition to the predominant schorlomite component, the crystals examined in this work contain significant (>15 mol.%) proportions of andradite (Ca₃Fe³⁺₂Si₃O₁₂), morimotoite (Ca₃Fe²⁺TiSi₃O₁₂), and Ca₃MgTiSi₃O₁₂. The importance of accurate quantitative determination and assignment of Fe, Ti and other cations to the crystallographic sites for petrogenetic studies is discussed.

Multi‐sensor Image Maps from SPOT,ERS and JERS

Abstract

Image mapping using data from visible and infrared sensors has, as a major drawback, the frequent cloud cover experienced in many countries. This is one of the main reasons why topographic maps at 1:100,000 scale and larger are often outdated. The results of a study which investigated the possibilities of fusing up‐to‐date spaceborne microwave data with existing images from optical sensors for topographic map updating at a scale of 1:100, 000 are presented in this paper. A key issue researched was the influence of geometric distortions and corrections of remote sensing data on the results of pixel based digital image fusion. After having terrain‐geocoded and radiometrically enhanced imagery from the Landsat, SPOT, ERS‐1 and JERS‐1 satellites, the data were fused applying a variety of colour transformation techniques as well as statistical or arithmetic methods. Initially, the image fusion was implemented using images covering a test site in the north of The Netherlands in order to calibrate specified combinations and techniques in a rather flat area. With the experience gained, the remote sensing data acquired over the research site were processed. The research test site is located in a typical Developing Country in the humid Tropics, on the mountainous south‐west coast of Sumatra in Indonesia. The results of the various applied techniques and image combinations were evaluated with reference to their capability to overcome the cloud cover problem. New combinations of techniques and images were developed as result of an optimisation process. The research produced two prototypes of annotated 1:100,000 scale image maps containing fused, cloud‐free optical/microwave imagery.     

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.     

Cultures monoalgales: courte description et discussion d'une méthode permettant une observation à fort grossissement des cellules avant leur isolement à l'aide d'un emporte-pièce

A method allowing isolation of phytoplancton algae for unialgal cultures is briefly described. Advantages and limits of the method are discussed.     

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.     

Acid mine drainage at Cerro Rico de Potosí I: unabated high-strength discharges reflect a five century legacy of mining

Intensive mining and processing of Ag, Sn, Pb and Zn ores have occurred in various locations within and around the city of Potosí, Bolivia since 1545. Surface and subsurface waters, stream sediments and soils are contaminated with various ecotoxic metals in the headwaters of the economically vital, yet highly impacted, upper Rio Pilcomayo watershed. Previous studies have documented downstream trace metal contamination, however, not addressed specific sources. The AMD discharges identified in this study help link downstream pollution to primary origins. The majority of AMD would be considered high-strength due to metal concentrations and acidity orders of magnitude greater than typical AMD. Discharges from both operating and abandoned portals as well as tailings-related deposits displayed a high degree of heterogeneity with total metal concentrations ranging from 0.11 to 7480, <0.022 to 889, <0.0006 to 65.3, <0.001 to 310, 0.12 to 72,100, 0.3 to 402, <0.012 to 34.8, and 0.24 to 19,600 mg/L of Al, As, Cd, Cu, Fe, Mn, Pb and Zn, respectively. Net acidity and pH ranged from −10 to 246,000 mg/L as CaCO₃ equivalent and 0.90–6.94 standard units, respectively. Data were gathered during two sampling events centered around the most extreme periods of the dry and wet seasons of one water-year. Loadings to local streams were marginally greater for most metals in the wet season. If observed loadings are historically representative, Cerro Rico AMD has contributed thousands of tonnes of ecotoxic metals to the upper Rio Pilcomayo over the last five centuries. Metal and hydrogen ion concentrations in the majority of AMD sampled were several orders of magnitude above discharge limits set by the Bolivian government, yet no action has historically or contemporarily been taken.     

Stratospheric methane and nitrogen dioxide from infrared spectra

Values of the mixing ratio by volume of stratospheric NO₂ and CH₄ deduced from infrared spectra taken by means of balloon-borne spectrometers are presented. Possible evidence for the presence of formaldehyde in the stratosphere is also given.