Petrochronology of oxidized granulites from southern Peru

Sapphirine–quartz granulites from the Cocachacra region of the Arequipa Massif in southern Peru record early Neoproterozoic ultrahigh‐temperature metamorphism. Phase equilibrium modelling and zircon petrochronology are used to quantify timing and pressure–temperature (P–T) conditions of metamorphism. Modelling of three magnetite‐bearing sapphirine–quartz samples indicates peak temperatures of >950°C at ~0.7 GPa and a clockwise P–T evolution. Elevated concentrations of Al in orthopyroxene are also consistent with ultrahigh‐temperature conditions. Neoblastic zircon records ages of c. 1.0–0.9 Ga that are interpreted to record protracted ultrahigh‐temperature metamorphism. Th/U ratios of zircon of up to 100 reflect U‐depleted whole‐rock compositions. Concentrations of heavy rare earth elements in zircon do not show systematic trends with U–Pb age but do correlate with variable whole‐rock compositions. Very large positive Ce anomalies in zircon from two samples probably relate to strongly oxidizing conditions during neoblastic zircon crystallization. Low concentrations of Ti‐in‐zircon (<10 ppm) are interpreted to result from reduced titania activities due to the strongly oxidized nature of the granulites and the sequestration of titanium‐rich minerals away from the reaction volume. Whole‐rock compositions and oxidation state have a strong influence on the trace element composition of metamorphic zircon, which has implications for interpreting the geological significance of ages retrieved from zircon in oxidized metamorphic rocks.     

Oxygen isotope study of the Long Valley magma system, California: isotope thermometry and convection in large silicic magma bodies

Products of voluminous pyroclastic eruptions with eruptive draw-down of several kilometers provide a snap-shot view of batholith-scale magma chambers, and quench pre-eruptive isotopic fractionations (i.e., temperatures) between minerals. We report analyses of oxygen isotope ratio in individual quartz phenocrysts and concentrates of magnetite, pyroxene, and zircon from individual pumice clasts of ignimbrite and fall units of caldera-forming 0.76 Ma Bishop Tuff (BT), pre-caldera Glass Mountain (2.1-0.78 Ma), and post-caldera rhyolites (0.65-0.04 Ma) to characterize the long-lived, batholith-scale magma chamber beneath Long Valley Caldera in California. Values of '¹⁸O show a subtle 1‰ decrease from the oldest Glass Mountain lavas to the youngest post-caldera rhyolites. Older Glass Mountain lavas exhibit larger (~1‰) variability of '¹⁸O(quartz). The youngest domes of Glass Mountain are similar to BT in '¹⁸O(quartz) values and reflect convective homogenization during formation of BT magma chamber surrounded by extremely heterogeneous country rocks (ranging from 2 to +29‰). Oxygen isotope thermometry of BT confirms a temperature gradient between "Late" (815 °C) and "Early" (715 °C) BT. The '¹⁸O(quartz) values of "Early" and "Late" BT are +8.33 and 8.21‰, consistent with a constant '¹⁸O(melt)=7.8ǂ.1‰ and 100 °C temperature difference. Zircon-melt saturation equilibria gives a similar temperature range. Values of '¹⁸O(quartz) for different stratigraphic units of BT, and in pumice clasts ranging in pre-eruptive depths from 6 to 11 km (based on melt inclusions), and document vertical and lateral homogeneity of '¹⁸O(melt). Worldwide, five other large-volume rhyolites, Lava Creek, Lower Bandelier, Fish Canyon, Cerro Galan, and Toba, exhibit equal '¹⁸O(melt) values of earlier and later erupted portions in each of the these climactic caldera-forming eruptions. We interpret the large-scale '¹⁸O homogeneity of BT and other large magma chambers as evidence of their longevity (>10⁵ years) and convection. However, remaining isotopic zoning in some quartz phenocrysts, trace element gradients in feldspars, and quartz and zircon crystal size distributions are more consistent with far shorter timescales (10²-10⁴ years). We propose a sidewall-crystallization model that promotes convective homogenization, roofward accumulation of more evolved and stagnant, volatile-rich liquid, and develops compositional and temperature gradients in pre-climactic magma chamber. Crystal + melt + gas bubbles mush near chamber walls of variable '¹⁸O gets periodically remobilized in response to chamber refill by new hotter magmas. One such episode of chamber refill by high-Ti, Sr, Ba, Zr, and volatile-richer magma happened 10³-10⁴ years prior to the 0.76-Ma caldera collapse that caused magma mixing at the base, mush thawing near the roof and walls, and downward settling of phenocrysts into this hybrid melt.     

A Simple Model Of The Convective Internal Boundary Layer And Its Application To Surface Heat Flux Estimates Within Polynyas

A simple model of the convective (thermal) internalboundary layer has been developed for climatologicalstudies of air-sea-ice interaction, where in situobservations are scarce and first-order estimates ofsurface heat fluxes are required. It is amixed-layer slab model, based on a steady-statesolution of the conservation of potentialtemperature equation, assuming a balance betweenadvection and turbulent heat-flux convergence. Boththe potential temperature and the surface heat fluxare allowed to vary with fetch, so the subsequentboundary-layer modification alters the fluxconvergence and thus the boundary-layer growth rate.For simplicity, microphysical and radiativeprocesses are neglected.The model is validated using several case studies.For a clear-sky cold-air outbreak over a coastalpolynya the observed boundary-layer heights,mixed-layer potential temperatures and surface heatfluxes are all well reproduced. In other cases,where clouds are present, the model still capturesmost of the observed boundary-layer modification,although there are increasing discrepancies withfetch, due to the neglected microphysical andradiative processes. The application of the model toclimatological studies of air-sea interaction withincoastal polynyas is discussed.     

Growth mechanisms and geochemistry of carbonate concretions from the Cambrian Wheeler Formation (Utah,USA)

Carbonate concretions provide unique records of ancient biogeochemical processes in marine sediments. Typically, they form in organic‐rich mudstones, where a significant fraction of the bicarbonate required for carbonate precipitation is supplied from the decomposition of organic matter in the sediments. As a result, carbonates that comprise concretions are usually characterized by broad ranges in δ¹³C and include values that are significantly depleted relative to seawater. This article reports results from a physical, petrographic and geochemical analysis of 238 concretions from the Wheeler Formation (Cambrian Series 3), Utah, USA, which are unusual in several respects. Most prominently, they formed in organic‐poor mudstones (total organic carbon = 0·1 to 0·5%) and are characterized by a narrow range of δ¹³C that onlaps the range of contemporaneous seawater values. Subtle centre to edge trends in δ¹³C demonstrate that concretion precipitation was initiated by local chemical gradients set up by microbial activity in the sediments, but was sustained during growth by a large pool of inorganic bicarbonate probably derived from alkaline bottom waters. The large inorganic pool appears to have been important in facilitating rapid precipitation of the concretion matrix, which occurred via both displacive and replacive carbonate precipitation during early diagenesis. Stable isotope data from cogenetic pyrite (δ³⁴S) and silica (δ¹⁸O) phases provide insight into the evolution of biogeochemical processes during concretion growth, and suggest that concretions were formed almost entirely during sulphate reduction, with only minor modification thereafter. Concretions of the Wheeler Formation appear to represent an end‐member system of concretion formation in which rapid growth was promoted by ions supplied from sea‐water. As such, they offer insight into the spectrum of processes that may influence the growth of carbonate concretions in marine sediments.     

Comparison of crude oils and their alteration products

A simple method is proposed for using gas Chromatographic data on the high molecular weight saturated fractions of crude oils to make comparisons of source materials, migration mechanisms and, in particular, alteration processes within reservoirs. The preferential loss of normal alkanes by bacterial attack on a light crude is one of several processes readily followed using this scheme.     

Interstitial water chemistry of Jamaican reef sediment: sulfate reduction and submarine cementation

Chemical and isotopic analyses of pore waters from Jamaican reef sediment suggest the importance of microbial sulfate reduction as a major control upon the origin, distribution, and composition of submarine cements in this fringing reef setting. Fore-reef sediment pore waters exhibit active sulfate reduction and enrichment in ¹⁸O which is consistent with associated active magnesian calcite cementation, alkalinity consumption, and cement enrichment in ¹⁸O. Conversely, lack of widespread submarine cementation in the back-reef corresponds to the diminished resupply of sulfate coupled with input of CO₂-charged meteoric water from a nearby unconfined aquifer into the more stagnant pore waters which lower pore-water magnesian calcite saturation states and preclude active submarine cementation.     

Geochemical reconstruction of late Holocene drainage and mixing in Kluane Lake,Yukon Territory

The level of Kluane Lake in southwest Yukon Territory, Canada, has fluctuated tens of metres during the late Holocene. Contributions of sediment from different watersheds in the basin over the past 5,000 years were inferred from the elemental geochemistry of Kluane Lake sediment cores. Elements associated with organic material and oxyhydroxides were used to reconstruct redox fluctuations in the hypolimnion of the lake. The data reveal complex relationships between climate and river discharge during the late Holocene. A period of influx of Duke River sediment coincides with a relatively warm climate around 1,300 years BP. Discharge of Slims River into Kluane Lake occurred when Kaskawulsh Glacier advanced to the present drainage divide separating flow to the Pacific Ocean via Kaskawulsh and Alsek rivers from flow to Bering Sea via tributaries of Yukon River. During periods when neither Duke nor Slims river discharged into Kluane Lake, the level of the lake was low and stable thermal stratification developed, with anoxic and eventually euxinic conditions in the hypolimnion.     

The accuracy of methods used to estimate the whole-lake accumulation rate of organic carbon, major cations, phosphorus and heavy metals in sediment

The accuracy of three methods used to estimate the whole-lake accumulation rate of chemicals in sediment, the simple mean accumulation rate, regression against water depth and the mean accumulation rate in sedimentation zones, was assessed. The concentrations and accumulation rates of organic carbon, four major cations, phosphorus and four heavy metals in the 1902 to 1988 sediment layer at 43 sites in Kassjön were used and the three methods gave identical results. The accuracy of the simple mean accumulation rate method using 5 or 10 sites was investigated using Monte Carlo simulation and both versions gave accurate results. If the method used the dry sediment accumulation rate at 5 or 10 sites, along with chemical concentration at one central site, then the errors were less than ±10% for five of the chemicals and larger for the others (?20 or 20–40%), although the direction of the bias was predictable. If chemical accumulation rate at the central site only was used to estimate the whole-lake value, the bias increased to 25% for the major cations, 50% for the heavy metals and P, and 85% for organic carbon. Having 43 sites in Kassjön meant that the true whole-lake chemical accumulation rate was known and so the accuracy of the methods and their variants could be assessed for the first time. These findings allow the particulars of the simple mean accumulation rate method to be chosen to suit the accuracy needed for a palaeolimnological investigation.     

The Earthquake Readiness Scale: The Development of a Valid and Reliable Unifactorial Measure

Preparedness is a key dependent variable in many studies examining people’s response to disasters such as earthquakes. A feature of many studies on this issue, however, is the lack of attention given to psychometric issues when constructing measures of preparedness. With regard to earthquake preparation, for example, many studies could be greatly improved by the use of a valid and reliable measure of preparedness. This research developed such a measure that assessed both low-level preparedness, such as having an emergency kit, and high-level preparedness, such as altering home structures to mitigate damage. Studies of Wellington (New Zealand) residents using two samples totalling n=652 showed that 23 items measuring these different aspects of earthquake preparation could be combined into a reliable, valid, unifactorial scale. This brief scale should have utility in multivariate studies of earthquake preparation, either as a dependent variable, where preparation is the outcome variable of primary interest, or as one of several independent variables, where preparation and other measures predict another outcome variable.