WEATHERING BY WETTING AND DRYING: SOME EXPERIMENTAL RESULTS

A series of experiments on sandstone and dolerite was undertaken in an attempt to better understand the wetting and drying weathering process. As rock samples are frequently subjected to wet–dry cycles within the simulation of other weathering mechanisms (e.g. freeze–thaw), three common methods of moisture application were used and the influences of these evaluated. It was found that the method of moisture application could affect the nature of the weathering products resulting from wetting and drying. It was also observed that there were changes in the internal properties of the rock (e.g. porosity/microporosity) and that these could influence the synergistic operation of other weathering processes. Although not all of the observations could be explained, it is apparent that wetting and drying has both a direct and an indirect effect on the weathering of rock that has not been taken into account in simulations. Greater cognizance needs to be given to the role of this process both in the field and in laboratory simulations.     

Adakite-like Lavas from Antisana Volcano (Ecuador): Evidence for Slab Melt Metasomatism Beneath Andean Northern Volcanic Zone

Extensive sampling of the Antisana volcano in Ecuador (NorthernVolcanic Zone of the Andes) has revealed the presence of adakite-likerocks throughout the edifice, i.e. rocks with geochemical characteristicsclose, but not identical, to those of slab melts. Two main volcanicgroups have been distinguished, characterized by two distinctevolutionary trends. The AND group, mostly composed of andesites,shows the clearest adakitic characteristics such as high La/Yband Sr/Y ratios and low heavy rare earth element (HREE) contents.The CAK group, composed of high-K andesites and dacites, displaysless pronounced adakitic-like characteristics. Although themore basic rocks of each group are difficult to distinguishon many geochemical diagrams, a geochemical study shows thatthe evolution of the AND and CAK groups is dominated by differentpetrogenetic processes. The isotopic characteristics of theCAK rocks suggest that evolution of this group is dominatedby a limited assimilation–fractional crystallization processwithin the granitic continental basement of the cordillera.In the AND group, the abundances of incompatible elements, suchas Nb or HREE, suggest that the series was produced by a partialmelting process in a mantle rich in garnet, amphibole and/orclinopyroxene. Such a mantle source has been demonstrated (experimentallyand by exhumed mantle xenoliths) to be produced in subductionzones where slab melts react with and metasomatize the mantlewedge. In Ecuador, magmas erupted in the Western Cordillera(trenchward relative to Antisana volcano) are true adakites,suggesting that slab melts can be responsible for the metasomatismof the mantle wedge beneath the NVZ in Ecuador. If mantle convectioncan drag down this modified mantle beneath Antisana volcano,destabilization of metasomatic amphibole at appropriate pressuresin this modified garnetiferous mantle can adequately explainthe formation and the geochemical features of Antisana lavas. KEY WORDS: subduction; adakite; metasomatism; Ecuador; AFC; Sr and Nd isotopes     

The effects of sea level and palaeotopography on lithofacies distribution and geometries in heterozoan carbonates, south-eastern Spain

This study utilized three-dimensional exposures to evaluate how sea-level position and palaeotopography control the facies and geometries of heterozoan carbonates. Heterozoan carbonates were deposited on top of a Neogene volcanic substrate characterized by palaeotopographic highs, palaeovalleys, and straits that were formed by subaerial erosion, possibly original volcanic topography, and faults prior to carbonate deposition. The depositional sequence that is the focus of this study (DS1B) consists of 7–10 fining upward cycles that developed in response to relative sea-level fluctuations. A complete cycle has a basal erosion surface overlain by deposits of debrisflows and high-density turbidity currents, which formed during relative sea-level fall. Overlying tractive deposits most likely formed during the lowest relative position of sea level. Overlying these are debrites grading upward to high-density turbidites and low-density turbidites that formed during relative sea-level rise. The tops of the cycles consist of hemipelagic deposits that formed during the highest relative position of sea level. The cycles fine upward because upslope carbonate production decreased as relative sea level rose due to less surface area available for shallow-water carbonate production and partial drowning of substrates. The cycles are dominated by two end-member types of facies associations and stratal geometries that formed in response to fluctuating sea-level position over variable substrate palaeotopography. One end-member is termed ‘flank flow cycle’ because this type of cycle indicates dominant sediment transport down the flanks of palaeovalleys. Those cycles drape the substrate, have more debrites, high-density turbidites and erosion on palaeovalley flanks, and in general, the lithofacies fine down the palaeovalley flanks into the palaeovalley axes. The second end-member is termed ‘axial flow cycle’ because it indicates a dominance of sediment transport down the axes of palaeovalleys. Those cycles are characterized by debrites and high-density turbidites in palaeovalley axes, and lap out of strata against the flanks of palaeovalleys. Where and when an axial flow cycle or flank flow cycle developed appears to be related to the intersection of sea level with areas of gentle or steep substrate slopes, during an overall relative rise in sea level. Results from this study provide a model for similar systems that must combine carbonate principles for sediment production, palaeotopographic controls, and physical principles of sediment remobilization into deep water.     

BOOK REVIEWS

Abstract

A distributed eco-hydrological model based on soil—vegetation—atmosphere transfer processes is applied to estimate actual evapotranspiration (ET) and gross primary production (GPP) over the Wuding River basin, Loess Plateau, China, based on digital elevation model, vegetation and soil information between 2000 and 2003 over three grid sizes: 250 m, 1 km and 8 km. The spatial patterns of annual ET and GPP are related to precipitation variability and land-use/cover conditions. The grid size is shown to affect the spatial patterns of annual ET and GPP, the effect on GPP being more significant than that on ET. Geostatistical and regression analyses demonstrate that precipitation and vegetation influence the scaling effect of ET and GPP in a complex way. When precipitation is high, the scaling effect of ET is more dependent on precipitation. The scaling effect of ET and GPP from 1-km to 8-km grid size is much larger than that from 250-m to 1-km grid size, showing the 1-km grid size to be a feasible choice for simulation of their spatial patterns. Although the annual GPP is more sensitive to the grid size than annual ET, both daily ET and daily GPP averaged over the whole basin seem to be insensitive to the grid size, illustrating that the coarse grid size can be used to simulate spatially-averaged variables without losing much accuracy.     

Optimizing bioventing in shallow vadose zones and cold climates

Abstract

This paper describes a bioventing study design and initial activities applied to a JP-4 jet fuel spill at Eielson Air Force Base, Alaska. The primary objectives of the project were to investigate the feasibility of using bioventing technology to remediate JP-4 jet fuel contamination in a sub-arctic environment and to determine to what degree the biodegradation rate of JP-4 soil contaminants could be enhanced by increasing soil temperature, both actively by circulating heated groundwater and passively by utilizing solar energy. Biodegradation rates at the bioventing site remained relatively high during the winter months in the active-warming test plot and were consistently higher than those observed in the passive-warming and control test plots. These studies suggest that an active-warming system operated in conjunction with bioventing is a useful method for remediating fuel-contaminated areas in cold climates.     

Noble gases in pillow basalt glasses from the northern Mariana Trough back-arc basin

Noble gas concentrations and isotopic compositions have been measured in eight samples of pillow basalt glasses collected from seven different localities along 250 km of the Mariana Trough spreading and rifting axis. The samples have uniform and mid-ocean ridge basalt (MORB)-like ³He/⁴He values of 9–12 × 10^–6 (6.4–8.6 times atmospheric) despite large variations in ⁴He. Concentrations of the noble gases Ne, Ar, Kr, and Xe show much smaller variations between samples, but larger variations in isotopic compositions of Ne, Ar, and Xe. Excess radiogenic ²¹Ne is observed in some samples. ⁴⁰Ar/³⁶Ar varies widely (atmospheric to 1880). Kr is atmospheric in composition for all samples. Some samples show a clear excess ¹²⁹Xe, which is a well-known MORB signature. Isotopic compositions of the heavier noble gases (Ar, Kr, and Xe) in some samples, however, show more atmospheric components. These data reflect the interaction of a MORB-like magma with an atmospheric component such as seawater or of a depleted mantle source with a water-rich component that was probably derived from the subducting slab.     

Surge marks: are they water-escape structures?

In his recent paper on surge mark formation and morphology, Bull (1978) has provided considerable new and interesting information on these peculiar features. Of particular note is his observation that the laminae within surge marks are continuous and not dissected as would be expected if the surge marks were erosional rills: the previously proposed mechanism of formation (High & Picard, 1968; Picard & High, 1973). Consequently, it becomes necessary to formulate an alternative explanation for surge mark origin, and Bull (1978, p. 885) offers the suggestion that: ‘Surge marks may be the result of selective depositional/erosional processes together with external deformation pressures.’     

Vertical Profile of Night-Time Stratospheric OClO

The first night-time observation of the vertical profile of OClO wasperformed by the AMON balloon-borne spectrometer during the SESAME arcticcampaign, launched from Kiruna in northern Scandinavia. The flight, which tookplace inside the polar vortex on February 10, 1995, reveals mixing ratios of45±10 pptv at 20 km. These results are in excellent agreement with theREPROBUS 3D model simulations, which indicate that the observed OClOcorresponds to daytime ClO and BrO mixing ratios of 1.2 ppbv and 10 pptv,respectively.     

An Experimental Study of Nepheline-Kalsilite Exsolution

The nepheline-kalsilite exsolution reaction was studied isothermallybetween 400 and 700°C. Under nonaqueous conditions the mechanisminvolves nucleation of kalsilite and growth by diffusion ofthe alkalis. As predicted by simple nucleation theory, the nucleationrate and hence the over-all exsolution rate are strongly dependenton the supersaturation of the nepheline. A decrease in temperatureat constant composition increases the supersaturation and therebythe nucleation rate. This increased nucleation rate is opposedby the decrease in the growth rate due to slower volume diffusion.At a supersaturation of more than 8–10 mole per cent thenumber of nuclei is large and the over-all exsolution rate isdetermined primarily by the growth rate. The activation energyfor growth is 28 kcal/mole. An increase of two kilobars in thehydrostatic pressure has little effect on the kinetics of thereaction. Under nonhydrostatic conditions the exsolution rateincreases significantly because the nucleation rate is faster. Under hydrothermal conditions the ‘exsolution’ rateis approximately two orders of magnitude faster due to a modificationin the mechanism. Partial dissolution of the original solidsolution in distilled water creates a condition of nonequilibriumin which the fluid is sodium-rich. Rapid alkali exchange eliminatesthis condition but produces the equilibrium compositions ofthe solids because kalsilite nucleates and grows in contactwith the fluid. The experimental evidence for this mechanismincludes X-ray diffraction data showing a gradual change inthe composition of the initial supersaturated solid, essentiallyidentical activation energies for growth under aqueous and nonaqueousconditions, and a lower percentage of oxygen isotope exchangethan ‘exsolution’ in the same experiment.     

Kinetics and Mechanism of Pyrite Exsolution from Pyrrhotite

Pyrite exsolution from pyrrhotite at 325 °C occurs by heterogeneousnucleation of pyrite and subsequent growth by volume diffusionof iron away from the nuclei. Sulfur atoms are required to moveonly short distances and although their diffusivity is muchlower than iron, their movement is not the rate determiningfactor. The exsolution rate is primarily dependent on the nucleationrate, which increases with the degree of supersaturation. Inaddition, the impurities in National Bureau of Standards 55diron or 500 ppm of As, Sb, or Bi retard the exsolution rateby two or more orders of magnitude at 325 °C. This reductionis primarily the result of a lower nucleation rate and is believedto be due to a decreased vacancy mobility caused by a high bindingenergy of vacancies with the slow diffusing impurities. Thusthe strain associated with the nucleation cannot be as easilyrelieved. The impurities may also reduce the growth rate bycausing a decrease in mobility of the pyrite interface. The most important general aspect of this study is the effectof a few hundred parts per million of an impurity on the exsolutionrate of this reaction. This suggests that the rate of othermineral reactions may also be dependent on impurities; however,the importance of this factor in any particular mineral reactionrequires experimental verification.