Elemental and isotopic fractionation of Type B calcium-, aluminum-rich inclusions: experiments, theoretical considerations, and constraints on their thermal evolution

Experiments exposing Type B calcium-, aluminum-rich inclusion (CAI)-like melts at high temperatures to high vacuum or reducing hydrogen-rich gas mixtures were used to determine the rates and consequences of elemental and isotopic fractionation by evaporation. Silicon and magnesium were found to evaporate much faster than calcium and aluminum, and the resulting residual liquid trajectories in composition space are reproduced via a thermodynamic model for the saturation vapor pressure of the evaporating species. Isotopic fractionations associated with evaporation were measured for magnesium. The resulting relationship between fraction of magnesium lost and enrichment of the residue in the heavy isotopes of magnesium follows a Rayleigh fractionation curve with a fractionation factor that is close to, but not exactly, the theoretically expected value. The rate of evaporation is found to be a strong function of temperature, oxygen fugacity, and melt composition, which can be understood and modeled in terms of the dependence of the saturation vapor pressures on these variables. The relationship between evaporation rate, which we measure, and calculated saturation vapor involves empirical evaporation coefficients that we find to be significantly less than one (∼0.1). Analytical and numerical models are used to characterize how diffusion in both the melt and in the surrounding gas affects evaporation rates and the degree of chemical and isotopic fractionation. The experimental data and theoretical considerations are combined to give a parameterization of the rates and consequences of evaporation of Type B CAI-like liquids, which is then used to translate the measured isotopic fractionation of Type B CAIs into constraints on their thermal history. Cooling rates of the order of 10°C per hour are indicated.     

Short‐term erosion rates from a 7Be inventory balance

Detailed soil erosion studies bene?t from the ability to quantify the magnitude of erosion over time scales appropriate to the process. An inventory balance for ⁷Be was used to calculate sediment erosion in a 30·73 m² plot during a series of runoff‐producing thunderstorms occurring over three days at the Deep Loess Research Station in Treynor, Iowa, USA. The inventory balance included determination of the pre‐ and post‐storm ⁷Be inventories in the soil, the atmospheric in?ux of ⁷Be during the event, and pro?les of the ⁷Be activity in the soil following the atmospheric deposition. The erosion calculated in the plot using the ⁷Be inventory balance was 0·058 g cm^?2, which is 23 per cent of the annual average erosion determined using ¹³⁷Cs inventories. The calculated erosion from the mass balance is similar to the 0·059 g cm^?2 of erosion estimated from the amount of sediment collected at the outlet of the 6 ha ?eld during the study period and the delivery ratio (0·64). The inventory balance of ⁷Be provides a new means for evaluating soil erosion over the time period most relevant to quantifying the prediction of erosion from runoff. Copyright © 2003 John Wiley & Sons, Ltd.     

Volatiles in glasses from Mauna Loa Volcano,Hawai'i: implications for magma degassing and contamination,and growth of Hawaiian volcanoes

Glasses from Mauna Loa pillow basalts, recent subaerial vents, and inclusions in olivine were analyzed for S, Cl, F, and major elements by electron microprobe. Select submarine glasses were also analyzed for H₂O and CO₂ by infrared spectroscopy. The compositional variation of these tholeiitic glasses is dominantly controlled by crystal fractionation and they indicate quenching temperatures of 1,115-1,196 °C. Submarine rift zone glasses have higher volatile abundances (except F) than nearly all other submarine and subaerial glasses with the maximum concentrations increasing with water depth. The overwhelming dominance of degassed glasses on the submarine flanks of Mauna Loa implies that much of volcano's recent submarine growth involved subaerially erupted lava that reached great water depths (up to 3.1 km) via lava tubes. Anomalously high F and Cl in some submarine glasses and glass inclusions indicate contamination possibly by fumarolic deposits in ephemeral rift zone magma chambers. The relatively high CO₂ but variable H₂O/K₂O and S/K₂O in some submarine rift zone glasses indicates pre-eruptive mixing between degassed and undegassed magma within Mauna Loa's rift system. Volatile compositions for Mauna Loa magmas are similar to other active Hawaiian volcanoes in S and F, but are less Cl-rich than Ll'ihi glasses. However, Cl/K2O ratios are similar. Mauna Loa and Ll'ihi magmas have comparable, but lower H₂O than those from Kilauea. Thus, Kilauea's source may be more H₂O-rich. The dissimilar volatile distribution in glasses from active Hawaiian volcanoes is inconsistent with predictions for a simple, concentrically zoned plume model.     

Chlorine-36 in groundwater of the United States: empirical data

Natural production of the radionuclide chlorine-36 (³⁶Cl) has provided a valuable tracer for groundwater studies. The nuclear industry, especially the testing of thermonuclear weapons, has also produced large amounts of ³⁶Cl that can be detected in many samples of groundwater. In order to be most useful in hydrologic studies, the natural production prior to 1952 should be distinguished from more recent artificial sources. The object of this study was to reconstruct the probable preanthropogenic levels of ³⁶Cl in groundwater in the United States. Although significant local variations exist, they are superimposed on a broad regional pattern of ³⁶Cl/Cl ratios in the United States. Owing to the influence of atmospherically transported ocean salt, natural ratios of ³⁶Cl/total Cl are lowest near the coast and increase to a maximum in the central Rocky Mountains of the United States. Electronic Publication     

Platinum-group elements (PGE) and rhenium in marine sediments across the Cretaceous-Tertiary boundary: constraints on Re-PGE transport in the marine environment

The nature of Re-platinum-group element (PGE; Pt, Pd, Ir, Os, Ru) transport in the marine environment was investigated by means of marine sediments at and across the Cretaceous-Tertiary boundary (KTB) at two hemipelagic sites in Europe and two pelagic sites in the North and South Pacific. A traverse across the KTB in the South Pacific pelagic clay core found elevated levels of Re, Pt, Ir, Os, and Ru, each of which is approximately symmetrically distributed over a distance of ∼1.8 m across the KTB. The Re-PGE abundance patterns are fractionated from chondritic relative abundances: Ru, Pt, Pd, and Re contents are slightly subchondritic relative to Ir, and Os is depleted by ∼95% relative to chondritic Ir proportions. A similar depletion in Os (∼90%) was found in a sample of the pelagic KTB in the North Pacific, but it is enriched in Ru, Pt, Pd, and Re relative to Ir. The two hemipelagic KTB clays have near-chondritic abundance patterns. The ∼1.8-m-wide Re-PGE peak in the pelagic South Pacific section cannot be reconciled with the fallout of a single impactor, indicating that postdepositional redistribution has occurred. The elemental profiles appear to fit diffusion profiles, although bioturbation could have also played a role. If diffusion had occurred over ∼65 Ma, the effective diffusivities are ∼10⁻¹³ cm²/s, much smaller than that of soluble cations in pore waters (∼10⁻⁶ cm²/s). The coupling of Re and the PGEs during redistribution indicates that postdepositional processes did not significantly fractionate their relative abundances. If redistribution was caused by diffusion, then the effective diffusivities are the same. Fractionation of Os from Ir during the KTB interval must therefore have occurred during aqueous transport in the marine environment. Distinctly subchondritic Os/Ir ratios throughout the Cenozoic in the South Pacific core further suggest that fractionation of Os from Ir in the marine environment is a general process throughout geologic time because most of the inputs of Os and Ir into the ocean have Os/Ir ratios ≥1. Mass balance calculations show that Os and Re burial fluxes in pelagic sediments account for only a small fraction of the riverine Os (<10%) and Re (<0.1%) inputs into the oceans. In contrast, burial of Ir in pelagic sediments is similar to the riverine Ir input, indicating that pelagic sediments are a much larger repository for Ir than for Os and Re. If all of the missing Os and Re is assumed to reside in anoxic sediments in oceanic margins, the calculated burial fluxes in anoxic sediments are similar to observed burial fluxes. However, putting all of the missing Os and Re into estuarine sediments would require high concentrations to balance the riverine input and would also fail to explain the depletion of Os at pelagic KTB sites, where at most ∼25% of the K-T impactor’s Os could have passed through estuaries. If Os is preferentially sequestered in anoxic marine environments, it follows that the Os/Ir ratio of pelagic sediments should be sensitive to changes in the rates of anoxic sediment deposition. There is thus a clear fractionation of Os and Re from Ir in precipitation out of sea water in pelagic sections. Accordingly, it is inferred here that Re and Os are removed from sea water in anoxic marine depositional regimes.     

Water quality impacts from mining in the Black Hills,South Dakota,USA

The focus of this research was to determine if abandoned mines constitute a major environmental hazard in the Black Hills. Many abandoned gold mines in the Black Hills contribute acid and heavy metals to streams. In some areas of sulfide mineralization local impacts are severe, but in most areas the impacts are small because most ore deposits consist of small quartz veins with few sulfides. Pegmatite mines appear to have negligible effects on water due to the insoluble nature of pegmatite minerals. Uranium mines in the southern Black Hills contribute some radioactivity to surface water, but the impact is limited because of the dry climate and lack of runoff in that area.     

Comparative study of activation energies of conductance and desiccation rates of some marine algae

Measurements of the activation energy of electrical conductance and desiccation rates on subtidal marine algae from Florida were compared to similar data from the Bay of Fundy, Nova Scotia, on intertidal marine algae frequently subjected to long periods of exposure to air. We have developed a method for calculating the reaction rate constant of desiccation of fully hydrated marine algae. Values of activation energies and desiccation rate constants are consistent with the requirements for survival of these algae under widely different environmental conditions.     

Predicted signatures of pulsed reconnection in ESR data

Early in 1996, the latest of the European inco-herent-scatter (EISCAT) radars came into operation on the Svalbard islands. The EISCAT Svalbard Radar (ESR) has been built in order to study the ionosphere in the northern polar cap and in particular, the dayside cusp. Conditions in the upper atmosphere in the cusp region are complex, with magnetosheath plasma cascading freely into the atmosphere along open magnetic field lines as a result of magnetic reconnection at the dayside magnetopause. A model has been developed to predict the effects of pulsed reconnection and the subsequent cusp precipitation in the ionosphere. Using this model we have successfully recreated some of the major features seen in photometer and satellite data within the cusp. In this paper, the work is extended to predict the signatures of pulsed reconnection in ESR data when the radar is pointed along the magnetic field. It is expected that enhancements in both electron concentration and electron temperature will be observed. Whether these enhancements are continuous in time or occur as a series of separate events is shown to depend critically on where the open/closed field-line boundary is with respect to the radar. This is shown to be particularly true when reconnection pulses are superposed on a steady background rate.     

Sampling Fauna in Stream Sediments as well as Groundwater Using One Net Sampler

Groundwater bores act as traps. Net samplers are regularly used for sampling this type of trap for fauna. To enable direct comparisons of faunal communities in groundwater bores and stream sediments, stream sediment tubes were built similar to groundwater bores and were sampled with net samplers for fauna. These stream sediment tubes consisted of a tube anchored in the stream sediment, also called interstitial space. To test the efficacy of this trap method in stream sediments, it was compared to another type of trap, Hahn's trap. Faunal communities sampled by a net in the stream sediment tubes did not differ hugely from fauna in Hahn's trap samples. Physical and chemical factors of sampled water in both the stream sediment tubes, the surrounding interstitial sediments and the second type of traps, Hahn's traps, showed that water in both the tubes and Hahn's traps was closely related to interstitial water. The net sampler is inexpensive and easy to handle. It is suggested that sampling stream tubes with nets may be an appropriate method for long‐term monitoring studies.