Bio-climatic imprints on a Holocene loess palaeosol from China

Micromorphology, heavy minerals, pollen and soil properties were examined in a typical Holocene loess profile in the north of the Loess Plateau, consisting of a palaeosol (locally known as the Ansai palaeosol) underlain by the Malan loess and overlain by modern loess. The palaeosol consists of an upper humus-rich (AB) horizon over a clay-rich (Bt) horizon. The humus-rich horizon is intensely weathered, contains precipitated calcitic material derived from the overlying modern loess, and has both high pollen content and diversity. Clay coatings in the clay-rich horizon indicate formation by eluviation–illuviation of clay. Pedogenetic characteristics and pollen analysis imply that the vegetation during the time of most intensive soil development is likely to have been a warm-temperate forest. A complex interpretation of the loess–palaeosol sequence recognizes several development stages. The phase of soil development, maximum and minimum limiting ages for which are ca. 8800 and 4400 ¹⁴C years BP, involved continuing but reduced loess deposition, and successive Holocene bio-climatic environment overprinted new features on the palaeosol.     

P–T–fO2 controls on a partly inverse chromite-bearing ultramafic intrusive: an evaluation from the Sukinda Massif, India

The chromites from the alpine type ultramafic intrusive of Sukinda, India, display a typical partly inverse spinel form and occur in two distinct zones: Brown Ore Zone (BOZ) and Grey Ore Zone (GOZ). The host ultramafites are mostly altered and are represented by the serpentinite, tremolite-talc(chlorite) schist, talc-serpentine schist and chlorite rock. The less altered variants are dunite, harzburgite and websterite. A dyke of orthopyroxenite runs through the main ultramafic body.The composition of olivine (Fo₉₂), orthopyroxene (En_92–89) and Al₂O₃ contents of the parental liquid (10.40–11.45%) determined from chromites, suggest that the parent melt is of boninitic affinity. The chemical plot of TiO₂ content against cr# of chromites corroborates a boninitic parental melt. The Fe–Mg partitioning in olivine and chromite depicts the temperature for chromitites as 1200 °C. A compositional plot of mg# and cr# suggests crystallization at high pressure conditions, corresponding to the kimberlite xenolith field. From the P–T diagram of pyrolite melting and mineral assemblage, the pressure of crystallization is stipulated to be ≥1.2 GPa. The f_O2 values estimated from Fe³⁺/Cr+Al+Fe³⁺ ratios range from 10^−8.3 to 10^−9.3 for the GOZ and 10^−7.1 to 10^−7.3 for the BOZ. The f_O2 values together with the pressure range suggest crystallization at upper mantle conditions. The heterogeneity in chemical composition and f_O2 conditions for the GOZ and BOZ could be linked to heterogeneity in the upper mantle.     

A Physical and Numerical Investigation on the Stability of Shallow Tunnels in Strain Softening Media

Summary The behaviour up to failure of shallow underground openings is discussed on the basis of some laboratory, small-scale model tests and of finite element simulation. The experimental results are first illustrated. They were obtained from two-dimensional (plane strain) and three-dimensional tunnel models tested under standard gravity conditions. Then, the phenomenon of strain localisation that characterizes the medium surrounding the model tunnels is discussed, recalling two alternative approaches for its numerical interpretation. On this basis, a finite element procedure for strain softening analyses is outlined and applied to the simulation of the tests in both two- and three-dimensional conditions. The comparison between experimental and numerical results leads to some conclusions on the influence of strain localisation on the overall behaviour of shallow tunnels and on the stability of their headings.     

Silica-rich Melts in Quartz Xenoliths from Vulcano Island and their Bearing on Processes of Crustal Anatexis and Crust-Magma Interaction beneath the Aeolian Arc, Southern Italy

Quartz-rich xenoliths in lavas and pyroclastic rocks from VulcanoIsland, part of the Aeolian arc, Italy, contain silicic meltinclusions with high SiO₂ (73–80 wt %) and K₂O (3–6wt %) contents. Two types of inclusions can be distinguishedbased on their time of entrapment and incompatible trace element(ITE) concentrations. One type (late, ITE-enriched inclusions)has trace element characteristics that resemble those of themetamorphic rocks of the Calabro-Peloritano basement of theadjacent mainland. Other inclusions (early, ITE-depleted) havevariable Ba, Rb, Sr and Cs, and low Nb, Zr and rare earth element(REE) contents. Their REE patterns are unfractionated, witha marked positive Eu anomaly. Geochemical modelling suggeststhat the ITE-depleted inclusions cannot be derived from equilibriummelting of Calabro-Peloritano metamorphic rocks. ITE-enrichedinclusions can be modelled by large degrees (>80%) of meltingof basement gneisses and schists, leaving a quartz-rich residuerepresented by the quartz-rich xenoliths. Glass inclusions inquartz-rich xenoliths represent potential contaminants of Aeolianarc magmas. Interaction between calc-alkaline magmas and crustalanatectic melts with a composition similar to the analysed inclusionsmay generate significant enrichment in potassium in the magmas.However, ITE contents of the melt inclusions are comparablewith or lower than those of Vulcano calc-alkaline and potassicrocks. This precludes the possibility that potassic magmas inthe Aeolian arc may originate from calc-alkaline parents throughdifferent degrees of incorporation of crustal melts. KEY WORDS: melt inclusions; crustal anatexis; magma assimilation; xenoliths; Vulcano Island     

Petrology and Geochemistry of Early Cretaceous Bimodal Continental Flood Volcanism of the NW Etendeka, Namibia. Part 1: Introduction, Mafic Lavas and Re-evaluation of Mantle Source Components

The bimodal NW Etendeka province is located at the continentalend of the Tristan plume trace in coastal Namibia. It comprisesa high-Ti (Khumib type) and three low-Ti basalt (Tafelberg,Kuidas and Esmeralda types) suites, with, at stratigraphicallyhigher level, interstratified high-Ti latites (three units)and quartz latites (five units), and one low-Ti quartz latite.Khumib basalts are enriched in high field strength elementsand light rare earth elements relative to low-Ti types and exhibittrace element affinities with Tristan da Cunha lavas. The unradiogenic²⁰⁶Pb/²⁰⁴Pb ratios of Khumib basalts are distinctive, most plottingto the left of the 132 Ma Geochron, together with elevated ²⁰⁷Pb/²⁰⁴Pbratios, and Sr–Nd isotopic compositions plotting in thelower ¹⁴³Nd/¹⁴⁴Nd part of mantle array (EM1-like). The low-Tibasalts have less coherent trace element patterns and variable,radiogenic initial Sr (     

The Solubility of Sulphur in Hydrous Rhyolitic Melts

Experiments performed at 2 kbar, in the temperature range 800–1000°C,with fO₂ between NNO–2·3 and NNO+2·9 (whereNNO is the nickel–nickel oxide buffer), and varying amountsof sulphur added to hydrous metaluminous rhyolite bulk compositions,were used to constrain the solubility of sulphur in rhyolitemelts. The results show that fS₂ exerts a dominant control onthe sulphur solubility in hydrous silicate melts and that, dependingon fO₂, a rhyolitic melt can reach sulphur contents close to1000 ppm at high fS₂. At fO₂ below NNO+1, the addition of ironto a sulphur-bearing rhyolite magma produces massive crystallizationof pyrrhotite and does not enhance the sulphur solubility ofthe melt. For a given fO₂, the melt-sulphur-content increaseswith fS₂. For fixed fO₂ and fS₂, temperature exerts a positivecontrol on sulphur solubilities, at least for fO₂ below NNO+1.The mole fraction of dissolved sulphur exhibits essentiallylinear dependence on fH₂S at low fO₂ and, although the experimentalevidence is less clear, on fSO₂ at high fO₂. The minimum insulphur solubility corresponds to the redox range where bothfH₂S and fSO₂ are approximately equal. A thermodynamic modelof sulphur solubility in hydrous rhyolite melts is derived assumingthat total dissolved sulphur results from the additive effectsof H₂S and SO₂ dissolution reactions. The model reproduces wellthe minimum of sulphur solubility at around NNO+1, in additionto the variation of the sulphide to sulphate ratio with fO₂.A simple empirical model of sulphur solubility in rhyoliticmelts is derived, and shows good correspondence between modeland observations for high-silica rhyolites. KEY WORDS: sulphur; solubility; rhyolite; thermodynamics; fO₂; fS₂     

Crustal Growth by Magmatic Accretion Constrained by Metamorphic P-T Paths and Thermal Models of the Kohistan Arc, NW Himalayas

Magmatic accretion is potentially an important mechanism inthe growth of the continental crust and the formation of granulites.In this study, the thermal evolution of a magmatic arc in responseto magmatic accretion is modeled using numerical solutions ofthe one-dimensional heat conduction equation. The initial andboundary conditions used in the model are constrained by geologicalobservations made in the Kohistan area, NW Himalayas. Takingconsideration of the preferred intrusion locations for basalticmagmas, we consider two plausible modes of magmatic accretion:the first involves the repeated intrusion of basalt at mid-crustaldepths (‘intraplate model’), and the second evaluatesthe simultaneous intrusion of basalt and picrite at mid-crustaldepths and the base of the crust respectively (‘double-platemodel’). The results of the double-plate model accountfor both the inferred metamorphic P–T paths of the Kohistanmafic granulites and the continental geotherm determined frompeak P–T conditions observed for granulite terranes. Thedouble-plate model may be applicable as a key growth processfor the production of thick mafic lower crust in magmatic arcs. KEY WORDS: thermal model; magmatic underplating; P–T path; granulite; lower crust     

The Significance of Multiple Saturation Points in the Context of Polybaric Near-fractional Melting

Experimental petrologists have successfully located basalticliquid compositions parental to mid-ocean ridge basalt thatare, within experimental resolution, multiply saturated withthree-phase harzburgite or four-phase lherzolite assemblageson their liquidus at some elevated pressure. Such an experimentalresult is a necessary consequence of any paradigm in which eruptedbasalts derive from single-batch primary liquids that equilibratewith a mantle residue and undergo no subsequent magma mixingbefore differentiation and eruption. Here we investigate whether,conversely, such evidence of multiple saturation is sufficientto exclude dynamic melting models wherein increments of meltare mixed after segregation from residues, during melt transportor in magma chambers. Using two independent models of crystal–liquidequilibria to simulate polybaric near-fractional peridotitemelting, we find that aggregate liquids from such melting processescan display near-intersections of liquidus surfaces too closeto distinguish experimentally from exact multiple saturationpoints. Given uncertainties in glass compositions, fractionationcorrections, experimental temperature and pressure conditions,and achievement of equilibrium, these results suggest that polybaricmixtures can in fact masquerade as mantle-equilibrated single-batchprimary liquids. Multiple saturation points on the liquidussurfaces of primitive basalts do, however, preserve informationabout the average pressure of extraction of their constituentincrements of liquid. KEY WORDS: mantle melting; basaltic volcanism; experimental igneous petrology; thermodynamic modelling; inverse method