Distribution of Ferric Iron in some Upper-Mantle Assemblages

The distribution of ferric iron among the phases of upper-mantlerocks, as a function of pressure (P), temperature (T) and bulkcomposition, has been studied using ⁵⁷Fe Mssbauer spectroscopyto determine the Fe³⁺/Fe ratios of mineral separates from 35peridotite and pyroxenite samples. The whole-rock Fe³⁺ complementof a peridotite is typically shared approximately evenly amongthe major anhydrous phases (spinel and/or garnet, orthopyroxeneand clinopyroxene), with the important exception of olivine,which contains negligible Fe³⁺. Whole-rock Fe³⁺ contents areindependent of the T and P of equilibration of the rock, butshow a well-defined simple inverse correlation with the degreeof depletion in a basaltic component. Fe³⁺ in spinel and inboth pyroxenes from the spinel Iherzolite facies shows a positivecorrelation with temperature, presumably owing to the decreasein the modal abundance of spinel. In garnet peridotites, theFe³⁺ in garnet increases markedly with increasing T and P, whereasthat in clinopyroxene remains approximately constant. The complexnature of the partitioning of Fe³⁺ between mantle phases resultsin complicated patterns of the activities of the Fe³⁺ -bearingcomponents, and thus in calculated equilibrium f_O2, which showlittle correlation with whole-rock Fe³⁺ or degree of depletion.Whether Fe³⁺ is taken into account or ignored in calculatingmineral formulae for geothermobarometry can have major effectson the resulting calculated T and P. For Fe-Mg exchange geothermometers,large errors must occur when applied to samples more oxidizedor reduced than the experimental calibrations, whose f_O2 conditionsare largely unknown. Two-pyroxene thermometry is more immuneto this problem, and probably provides the most reliable P—Testimates. Accordingly, the convergence of P—T valuesderived for a given garnet peridotite assemblage may not necessarilybe indicative of mineral equilibrium. The prospects for thecalculation of accurate Fe³⁺ contents from electron microprobeanalyses by assuming stoichiometry are good for spinel, uncertainfor garnet, and distinctly poor for pyroxenes. KEY WORDS: mantle; oxidation; partitioning; peridotite; thermobarometry ^*Corresponding author. Present address: School of Earth and Ocean Sciences, University of Victoria, P.O. Box 1700, Victoria, B.C., V8W 2Y2, Canada     

The Sulfide Capacity and the Sulfur Content at Sulfide Saturation of Silicate Melts at 1400{degrees}C and 1 bar

The solubility of sulfur as S^2– has been experimentallydetermined for 19 silicate melt compositions in the system CaO–MgO–Al₂O₃–SiO₂(CMAS)± TiO₂ ± FeO, at 1400°C and 1 bar, using CO–CO₂–SO₂gas mixtures to vary oxygen fugacity (fO₂) and sulfur fugacity(fS₂). For all compositions, the S solubility is confirmed tobe proportional to (fS₂/fO₂)^1/2, allowing the definition ofthe sulfide capacity (C_S) of a silicate melt as C_S = [S](fO₂/fS₂)^1/2.Additional experiments covering over 150 melt compositions,including some with Na and K, were then used to determine C_Sas a function of melt composition at 1400°C. The resultswere fitted to the equation     

Matt Wilson structure: record of an impact event of possible Early Mesoproterozoic age,Northern Territory

The Matt Wilson structure is a circular 5.5 km-diameter structure in Early Mesoproterozoic or Neoproterozoic rocks of the Victoria Basin, Northern Territory. It lies in regionally horizontal to gently dipping Wondoan Hill and Stubb Formations (Tijunna Group) and Jasper Gorge Sandstone (Auvergne Group). An outer circumferential syncline with dips of 5?–?40° in the limbs surrounds an intermediate zone with faulted sandstone displaying horizontal to low dips, and a central steeply dipping zone about 1.5 km across. Several thrust faults in the outer syncline appear to indicate outward-directed forces. The central zone, marked by steeply dipping to overturned Tijunna Group and possibly Bullita Group sandstone and mudstone, indicates uplift of at least 300 m. The rocks are intensely fractured with some brecciation, and contain numerous planar to subtly undulating surfaces displaying striae which resemble shatter cleavage. Thin-sections of sandstone from the central area show zones of intense microbrecciation and irregular and planar fractures in quartz, but no melt-rocks have been identified. The planar fractures occur in multiple intersecting parallel sets typical of relatively low-level (5?–?10 GPa) shock-pressure effects. Alternative mechanisms, i.e. igneous intrusion, carbonate collapse, diapirism and regional deformation processes, have been discounted. The circular nature, central uplift, faulting, shatter features and planar fractures are all consistent with an impact origin. The Matt Wilson structure is most likely a deeply eroded impact structure in which the more highly shocked rocks of the original crater floor have been removed by erosion. Estimates of the age of the Auvergne and Tijunna Groups range from Early Mesoproterozoic (which we favour) to Late Neoproterozoic. Early Cambrian Antrim Plateau Volcanics near the impact structure show no signs of impact effects, allowing the age of impact to be constrained between Early Mesoproterozoic and Early Cambrian. The presence of widespread soft-sediment deformation features, apparently confined to a single horizon in the Saddle Creek Formation some 700?–?1000 m stratigraphically higher in the Auvergne Group than the rocks at the impact site, and apparently increasing in thickness towards the Matt Wilson structure, lead us to speculate that this probable event horizon is related to the impact event: if correct the impact occurred during deposition of the Saddle Creek Formation.     

Element Mobility During Incipient Granulite Formation at Kabbaldurga, Southern India

At Kabbaldurga, infiltration of carbonic fluids along a systemof ductile shears and foliation planes has led to partial transformationof Archaean grey biotite–hornblende gneiss to coarse-grainedmassive charnockite at about 2.5 b.y. ago. The dehydration ofthe gneiss assemblage was induced by a marked metasomatic changeof the reacting system from granodioritic to granitic, and obviouslytook place under conditions of an open system at 700–750?C and 5–7 kb. Extensive replacement of plagioclase (An_16–30)by K-feldspar through Na, Ca–K exchange reactions withthe ascending carbonic fluids led to strong enrichment in K,Rb, Ba, and SiO₂, and to a depletion in Ca. Progressive dissolutionof hornblende, biotite, magnetite, and the accessory mineralsapatite and zircon resulted in a marked depletion in Fe, Mg,Ti, Zn, V, P, and Zr. Most important is the recognition of REEmobility: with advancing charnockitization, the moderately fractionatedREE distribution patterns of the grey gneisses (La_N270; La_N/Yb_N= 5–20; Eu_N27; Eu/Eu^* = 0.6–0.3) give way to stronglyfractionated REE patterns with a positive Eu-anomaly (La_N200;La_N/Yb_N = 20–80; Eu_N22; Eu/Eu^* = 0.6–1.8). The systematicdepletion especially in the HREE is due to the progressive dissolutionof zircon, apatite (and monazite), which strongly concentratethe REE. Stable isotope data (¹⁸O of 6.9–8.0 per mille for gneissesand charnockites; ¹³C of –8.5 and –6.5 per millefor late carbonate) indicate a magmatogenic source for the carbonicfluids. In contrast to the currently favoured derivation ofcarbonic fluids by decarbonation of the upper mantle or degassingof underplated basaltic intrusions, it is discussed here thatabundant fluid inclusions in lower crustal charnockites providedan extensive reservoir of ‘fossil’ carbonic fluids.Shear deformation has tapped this reservoir and generated thechannel-ways for fluid ascent. Charnockitization of the Kabbaldurgatypethus appears to be a metasomatic process which is tectonicallycontrolled and restricted to the crustal level of the amphiboliteto granulite transition.     

Effect of Silica Activity on OH- IR Spectra of Olivine: Implications for Low-aSiO2 Mantle Metasomatism

Hydrogen solubility and hydroxyl substitution mechanism in olivineat upper-mantle conditions are not only a function of pressure,temperature, water fugacity and hydrogen fugacity, but are alsoinfluenced by silica activity. Olivine synthesized in equilibriumwith magnesiowüstite displays hydroxyl stretching bandsin the wavenumber range from 3640 to 3430 cm^–1. In contrast,olivine in equilibrium with orthopyroxene shows absorption bandsin a narrower wavenumber range from 3380 to 3285 cm^–1.The two fundamentally different spectra are assigned to hydroxylin tetrahedral and octahedral sublattices, respectively. Olivinein equilibrium with orthopyroxene is also less capable of incorporatinghydroxyl, relative to olivines in equilibrium with magnesiowüstite,by about a factor of ten. A comparison of spectra obtained aspart of this study with hydroxyl spectra of natural mantle olivinesshows that the latter display hydroxyl stretching patterns reminiscentof equilibrium with magnesiowüstite, although undoubtedlyolivine in the Earth’s mantle coexists with orthopyroxene.This may be attributed to a metasomatic overprint by a low-silicafluid and/or melt that was in reaction relationship with orthopyroxene.A likely metasomatic agent is a carbonatitic melt. When carbonatiticmelts decompose to oxides and CO₂, they may temporarily imposea low-aSiO₂ environment inherited by the olivine structure.If this suggestion proves true, Fourier transform IR spectroscopymay be used to fingerprint metasomatic episodes in the lithosphericmantle. KEY WORDS: FTIR spectrometry; olivine; mantle; metasomatism; water     

Tropical instability wave interactions within the Galápagos Archipelago

The effects of tropical instability waves (TIW) within the eastern equatorial Pacific during the boreal fall of 2005 were observed in multiple data sets. The TIW cause oscillations of the sea surface temperature (SST), meridional currents (V), and 20 °C isotherm (thermocline). A particularly strong 3-wave packet of ～15-day period TIW passed through the Galápagos Archipelago in Sep and Oct 2005 and their effects were recorded by moored near-surface sensors. Repeat Argo profiles in the archipelago showed that the large temperature (>5 °C) oscillations that occurred were associated with a vertical adjustment within the water column. Numerical simulations report strong oscillations and upwelling magnitudes of ～5.0 m d^?1 near the Tropical Atmosphere Ocean (TAO) buoy at 0°, 95°W and in the Archipelago at 92°W and 90°W. A significant biological response to the TIW passage was observed within the archipelago. Chlorophyll a measured by the Sea-viewing Wide Field-of-view Sensor (SeaWiFS) increased by >30% above 1998–2007 mean concentrations within the central archipelago. The increases coincide with coldest temperatures and the much larger increases within the archipelago as compared to those of 95°W indicate that TIW induced upwelling over the island platform itself brought more iron-enriched upwelling waters into the euphotic zone.     

Tectonic control on third‐order sequences in a siliciclastic ramp‐style basin: An example from the Roper Superbasin (Mesoproterozoic), northern Australia

TThe Roper Group is a cyclic, predominantly marine, siliciclastic succession of Calymmian (Early Mesoproterozoic) age. It has a distribution of at least 145 000 km² and a maximum known thickness of ～5000 m. In the Roper River district the middle part of the Roper Group (～1300 m thick) is characterised by the cyclical alternation of mudstone and sandstone units, and can be divided into six third‐order depositional sequences. A typical sequence is broadly progradational in aspect, and comprises a lower, mudstone‐rich, storm‐dominated shelf succession (up to 330 m thick), and a sequence‐capping unit dominated by tidal‐platform cross‐bedded sandstone (up to 80 m thick); both are interpreted as highstand systems tracts. Transgressive strata are poorly represented but where present are characterised by paralic to fluvial redbed assemblages that include ooidal ironstone. Roper Group sequences lack a distinct condensed section and sequence boundaries are mostly conformable. Erosional contacts separate mud‐rich shelf facies from sequence‐capping sandstones. We infer that these erosion surfaces were generated by episodic flexural tectonism, which also generated the accommodation and sediment supply for Roper sequences.     

The late Miocene to Pleistocene ice-rafting history of southeast Greenland

Analysis of a Miocene-Pleistocene ice-rafted debris (IRD) record from the western Irminger Basin provides evidence for the initiation and long-term behavior of the SE portion of the Greenland Ice Sheet. In the late Miocene (~7.3 Ma), IRD supply to Ocean Drilling Program site 918 increased significantly indicating that glaciers large enough to reach sea level were present in SE Greenland long before the onset of widespread Northern Hemisphere glaciation. IRD accumulated at this site throughout the Pliocene and Pleistocene, supporting the hypothesis that SE Greenland was a key nucleation area for the formation of the Greenland Ice Sheet. Since glacial onset, the western Irminger Basin IRD record is characterized by a succession of episodes with high IRD mass accumulation rates (MARs). The site 918 IRD record indicates that greatest iceberg production in SE Greenland occurred during major climatic transitions (e.g. widespread Northern Hemisphere glacial expansion at 2.7 Ma and the mid-Pleistocene climate shift at 0.9 Ma), and that SE Greenland sometimes also led the northern North Atlantic region in glacial response to climatic forcing (e.g. glacial intensification at ~4.8 and, along with NE Greenland, at ~3.5 Ma).     

Trace elements and polycyclic aromatic hydrocarbons (PAHs) concentrations in deep Gulf of Mexico sediments

The concentrations of polycyclic aromatic hydrocarbons (PAHs) and trace elements were determined for surface (top 2 cm) sediment samples collected during the deep Gulf of Mexico benthos (DGoMB) study .These elements and compounds are known to be toxic to organisms at high concentrations and may affect biological communities. There is no indication of major anthropogenic input of the elements Be, Co, Cr, Fe, Si, Tl, V, K, Mg, Ca, Sr and Zn, based on normalization to Al. The concentrations of these metals in the sediment are a function of the relative amounts of trace-metal-rich Mississippi River-derived silicate material and trace-metal-poor plankton-derived carbonate. This is not true for the elements Ba, Ni, Pb, Cd, As, Cu and Mn, whose concentrations show considerable scatter when normalized to Al and a general enrichment. On a normalized basis, Mn is enriched 5–10 fold, Cu and Ni 2–3 fold and Pb 2 fold over Mississippi River-derived material. These enrichments are likely the result of remobilization of metals from depths in the sediment column where reducing conditions exist. The Ba concentrations at selected sites are higher than those of average clay-rich sediments, but are typical of sediments from near oil well platforms in the northern Gulf of Mexico. In the case of Ba, it seems likely that the enrichments, as high as a factor of 10, are due to disposal of oil well drilling mud. The Ba-enriched samples are from the three shallowest water sites in the Mississippi Trough (sites MT1, 2 and 3) and from site C1 and WC5. All are in an area of intense petroleum exploration and development. PAH concentrations are also elevated at MT1, MT3 and C1. The total PAH concentration ranged from not detected (ND) to 1033 ng/g with a mean of 140 ng/g. Even at the sites most enriched in PAHs and trace elements, the concentrations are not at the levels expected to adversely affect the biota. However, these predicted non-effects are based on research using mostly near-shore estuarine species, not on the indigenous species at the sampling sites.