Origin of Archean migmatites from the Gwenoro Dam area,Zimbabwe-Rhodesia

Archean migmatites in the vicinity of Gwenoro Dam in Zimbabwe-Rhodesia are composed chiefly of trondhjemite gneiss (TR), mafic tonalite (MT), amphibolite (AM), leuco-trondhjemite veins (LTR), and pegmatites. The gneiss is intruded in nearby areas with small tonalite plutons (TN). Geochemical model studies together with field relationships are consistent with the following model for migmatite production: AM is produced by partial melting of a partly depleted ultramafic parent in which neither garnet nor amphibole remain in the residue; TR and TN are produced by partial melting of undepleted to variably depleted amphibolite in which garnet does not remain in the residue; MT is produced by mixing of plagioclase-rich TR with AM; and LTR represents the solid residue after fractional crystallization of TR.     

The Early Carboniferous paleomagnetic field of North America and its bearing on tectonics of the Northern Appalachians

We have obtained additional evidence for the Early Carboniferous paleomagnetic field for cratonic North America from study of the Barnett Formation of central Texas. A characteristic magnetization of this unit was isolated after thermal demagnetization at four sites (36 samples) out of eight sites (65 samples) collected. The mean direction of declination = 156.3°, inclination = 5.8° (N = 4 ,k = 905 , α₉₅ = 3.0°), corresponds to a paleomagnetic pole position at lat. = 49.1°N,long. = 119.3°E (dp = 1.5° , dm = 3.0°). Field evidence suggests that characteristic magnetization was acquired very early in the history of the rock unit whereas the rejected sites are comprised of weakly magnetized limestones dominated by secondary components near the present-day field direction. Comparison of the Barnett pole with other Early Carboniferous (Mississippian) paleopoles from North America shows that it lies close to the apparent polar wander path for stable North America and that the divergence of paleopoles from the Northern Appalachians noted previously for the Devonian persisted into the Early Carboniferous. We interpret this difference in paleopoles as further evidence for the Northern Appalachian displaced terrain which we refer to here as Acadia, and the apparent coherence of Late Carboniferous paleopoles as indicating a large (～1500 km) motion of Acadia with respect to stable North America over a rather short time interval in the Carboniferous.     

Late glacial and postglacial pollen and plant macrofossils from Lake West Okoboji, Northwestern Iowa

Pollen and plant macrofossils preserved in lake sediment from Lake West Okoboji, Dickinson County, Iowa, indicate how the vegetation of that area changed during the late glacial and postglacial. A closed coniferous forest, dominated by spruce and larch trees, produced the Picea-Larix pollen assemblage zone. Fir trees were a minor constituent of this forest; pine trees were probably absent. Black ash trees increased in abundance at Lake West Okoboji and by 13,500 yr ago were an important constituent of the forest. The sediment accumulation rate and the pollen influx were low throughout this time. Birch and alder pollen peaked in abundance approximately 11,800 yr ago. Pollen influx increased rapidly as birch and alder replaced coniferous trees on the uplands. A deciduous forest, containing abundant oak and elm trees, replaced the birch-alder-coniferous forest. This forest inhabited northwestern Iowa from approximately 11,000 to 9000 yr B.P. Nonarboreal species became prevalent between approximately 9000 and 7700 yr B.P. as prairie began to replace deciduous forest on the uplands. Charred remains of Amorpha canescens and other upland species attest to the presence of prairie fires as an aid in establishing prairie and destroying the forest. The pollen influx declined. The warmest, driest part of the postglacial occurred in northwestern Iowa from approximately 7700 to 3200 yr ago. Lake level fell 9 to 10 m, and prairie extended to the edge of the lake. Wet-ground weeds inhabited areas near lake level which were alternately flooded, then dry. Pollen influx was approximately 100 grains/cm²/yr during the driest time in this dry interval.Deciduous trees, particularly oaks, returned after approximately 3200 yr B.P. Prairie continued to occupy the uplands but trees were more common in the lowlying wet areas. Settlement by Europeans in northwestern Iowa about 1865 is marked by an increase in weed pollen. Macrofossil deposition changed in 1910 in response to the stabilization of lake level.     

Mineral/melt partitioning of trace elements during hydrous peridotite partial melting

This experimental study examines the mineral/melt partitioning of incompatible trace elements among high-Ca clinopyroxene, garnet, and hydrous silicate melt at upper mantle pressure and temperature conditions. Experiments were performed at pressures of 1.2 and 1.6 GPa and temperatures of 1,185 to 1,370 °C. Experimentally produced silicate melts contain up to 6.3 wt% dissolved H ₂O, and are saturated with an upper mantle peridotite mineral assemblage of olivine+orthopyroxene+clinopyroxene+spinel or garnet. Clinopyroxene/melt and garnet/melt partition coefficients were measured for Li, B, K, Sr, Y, Zr, Nb, and select rare earth elements by secondary ion mass spectrometry. A comparison of our experimental results for trivalent cations (REEs and Y) with the results from calculations carried out using the Wood-Blundy partitioning model indicates that H ₂O dissolved in the silicate melt has a discernible effect on trace element partitioning. Experiments carried out at 1.2 GPa, 1,315 °C and 1.6 GPa, 1,370 °C produced clinopyroxene containing 15.0 and 13.9 wt% CaO, respectively, coexisting with silicate melts containing ~1–2 wt% H ₂O. Partition coefficients measured in these experiments are consistent with the Wood-Blundy model. However, partition coefficients determined in an experiment carried out at 1.2 GPa and 1,185 °C, which produced clinopyroxene containing 19.3 wt% CaO coexisting with a high-H ₂O (6.26±0.10 wt%) silicate melt, are significantly smaller than predicted by the Wood-Blundy model. Accounting for the depolymerized structure of the H ₂O-rich melt eliminates the mismatch between experimental result and model prediction. Therefore, the increased Ca ²⁺ content of clinopyroxene at low-temperature, hydrous conditions does not enhance compatibility to the extent indicated by results from anhydrous experiments, and models used to predict mineral/melt partition coefficients during hydrous peridotite partial melting in the sub-arc mantle must take into account the effects of H ₂O on the structure of silicate melts.     

Ground water/surface water interaction in a fractured rock aquifer

In a recent field study of ground water/surface water interaction between a bedrock stream and an underlying fractured rock aquifer, it was determined that the majority of ground water discharge occurred through sparsely located vertical fractures. In this paper, the dominant mechanisms governing ground water/surface water exchange in such an environment are investigated using a numerical model. The study was conducted using several conceptual models based on the field study results. Although the field results provided the motivation for the modeling study, it was not intended to match modeling and field results directly. In addition, the extent of capture zones for discharging or recharging fractures was explored. The results of this study are intended to provide a better understanding of contaminant migration in the vicinity of bedrock streams. Based on the numerical results, the rate of ground water discharge (or recharge) was found to depend on the aperture size of the discharging feature, and on the distribution of hydraulic head with depth within the fracture network. It was determined that the extent of both the capture zone and reverse capture zone for an individual fracture can be extremely large, and will be determined by the height of the stream stage, the fracture apertures of the network, and the hydraulic-head distribution within the network. Because both the stream stage and the hydraulic-head distribution are transient, the size of the capture zone and/or the reverse capture zone for an individual fracture may change significantly over time. As a result, the migration path for contaminants within the fracture network and between the surface and subsurface will also vary significantly with time.     

Isotope Dilution MC-ICP-MS Rare Earth Element Analysis of Geochemical Reference Materials NIST SRM 610, NIST SRM 612, NIST SRM 614, BHVO-2G, BHVO-2, BCR-2G, JB-2, WS-E, W-2, AGV-1 and AGV-2

We present data for the concentrations of eleven rare earth elements (La, Ce, Pr, Nd, Sm, Eu, Gd, Dy, Er, Yb, Lu) in eleven international geochemical reference materials obtained by isotope dilution multi-collector inductively coupled plasma-mass spectrometry (MC-ICP-MS). We have analysed both rock powders and synthetic silicate glasses, and the latter provide precise data to support the use of these as reference materials for in situ trace element determination techniques. Our data also provide precise measurements of the abundance of mono-isotopic Pr in both glasses and powders, which allows more accurate constraints on the anomalous redox-related behaviour of Ce during geochemical processes. All materials were analysed in replicate providing data that typically reproduce to better than one percent. Sm/Nd ratios in all these materials also reproduce to better than 0.2% and are accurate to < 0.2% and can thus be used as calibrants for Sm-Nd geochronology. Our analyses agree well with existing data on these reference materials. In particular, for NIST SRM 610, USGS BHVO-2, AGV-1 and AGV-2, our measured REE abundances are typically within < 2% (and mostly 1%) of REE concentrations previously determined by isotope dilution analysis and thermal ionisation mass spectrometry, consistent with the higher degree of precision and accuracy obtained from isotope dilution techniques. Close agreement of results between basaltic glass reference materials USGS BHVO-2G and BCR-2G and the BHVO-2 and BCR-2 powders from which they were created suggests that little fractionation, concentration or dilution of REE contents occurred during glass manufacture.     

The influence of groundwater chemistry on arsenic concentrations and speciation in a quartz sand and gravel aquifera)

We examined the chemical reactions influencing dissolved concentrations, speciation, and transport of naturally occurring arsenic (As) in a shallow, sand and gravel aquifer with distinct geochemical zones resulting from land disposal of dilute sewage effluent. The principal geochemical zones were: (1) the uncontaminated zone above the sewage plume [350 μM dissolved oxygen (DO), pH 5.9]; (2) the suboxic zone (5 μM DO, pH 6.2, elevated concentrations of sewage-derived phosphate and nitrate); and (3) the anoxic zone [dissolved iron(II) 100–300 μM, pH 6.5–6.9, elevated concentrations of sewage-derived phosphate]. Sediments are comprised of greater than 90% quartz but the surfaces of quartz and other mineral grains are coated with nanometer-size iron (Fe) and aluminum (Al) oxides and/or silicates, which control the adsorption properties of the sediments. Uncontaminated groundwater with added phosphate (620 μM) was pumped into the uncontaminated zone while samples were collected 0.3 m above the injection point. Concentrations of As(V) increased from below detection (0.005 μM) to a maximum of 0.07 μM during breakthrough of phosphate at the sampling port; As(III) concentrations remained below detection. These results are consistent with the hypothesis that naturally occurring As(V) adsorbed to constituents of the coatings on grain surfaces was desorbed by phosphate in the injected groundwater. Also consistent with this hypothesis, vertical profiles of groundwater chemistry measured prior to the tracer test showed that dissolved As(V) concentrations increased along with dissolved phosphate from below detection in the uncontaminated zone to approximately 0.07 and 70 μM, respectively, in the suboxic zone. Concentrations of As(III) were below detection in both zones. The anoxic zone had approximately 0.07 μM As(V) but also had As(III) concentrations of 0.07–0.14 μM, suggesting that release of As bound to sediment grains occurred by desorption by phosphate, reductive dissolution of Fe oxides, and reduction of As(V) to As(III), which adsorbs only weakly to the Fe-oxide-depleted material in the coatings. Results of reductive extractions of the sediments suggest that As associated with the coatings was relatively uniformly distributed at approximately 1 nmol/g of sediment (equivalent to 0.075 ppm As) and comprised 20%-50% of the total As in the sediments, determined from oxidative extractions. Quartz sand aquifers provide high-quality drinking water but can become contaminated when naturally occurring arsenic bound to Fe and Al oxides or silicates on sediment surfaces is released by desorption and dissolution of Fe oxides in response to changing chemical conditions.

     

The Muralla Pircada—an ancient Andean debris flow retention dam, Santa Rita B archaeological site, Chao Valley, Northern Perú

Debris flows caused by El Niño events, earthquakes, and glacial releases have affected northern Perú for centuries. The Muralla Pircada, a northeast-trending, 2.5 km long stone wall east of the Santa Rita B archaeological site (Moche-Chimú) in the Chao Valley, is field evidence that ancient Andeans recognized and, more importantly, attempted to mitigate the effects of debris flows. The Muralla is upstream from the site and is perpendicular to local drainages. It is 1–2 m high, up to 5 m wide, and is comprised of intentionally-placed, well-sorted, well-rounded, 20–30 cm cobbles and boulders from nearby streams. Long axes of the stones are gently inclined and parallel local drainage. Case-and-fill construction was used with smaller cobbles and pebbles used as fill. Pre-Muralla debris flows are indicated by meter-sized, angular boulders that were incorporated in-place into construction of the dam and are now exposed in breeches in the dam. Post-Muralla debris flows in the Chao Valley are indicated by meter-sized, angular boulders that now abut the retention dam.     

Seasonal Variability of Adsorption and Exchange Equilibria in Soil Waters

Chemical analyses for major ions have been conducted on waters,collected on an approximately weekly basis over the period April, 1993 toNovember, 1996, that drain three small experimental ecosystems(sandboxes) at Hubbard Brook, New Hampshire. One sandbox is planted withpine trees, another with grass, and the third is left bare (actually itis covered sporadically by bryophytes and lichens). Results show linearcorrelations, independent of discharge, between the concentrations ofdissolved Na⁺ and K⁺ on the one hand andCa⁺⁺ and Mg⁺⁺ on the other for all threesandboxes. No correlations between singly charged and doubly chargedcations were found. These correlations are interpreted to represent cationexchange equilibria between soil waters and clay minerals plus soil organicmatter. The correlation slope, representing the exchange constant, for Na vsK is different for the pine-covered sandbox than for the other two whereasfor Ca vs Mg the correlation is independent of the presence or absence oftrees. We interpret this as representing a shift of cation exchangeequilibria in the pine sandbox by the activities of growing trees.Concentrations of Na, K, Ca, Mg, and H₄SiO₄from the barren and grass-lined sandboxes were found to vary seasonally witha marked sinusoidal pattern which was independent of the discharge from eachsandbox. (The discernment of a similar pattern in the tree lined sandbox wasdifficult due to a lack of discharge over much of the year.) Concentrationmaxima occurred in August and minima in February, and there is a closeparallelism with soil temperature. We interpret this as representingtemperature induced variations in cation exchange equilibria and silicaadsorption. Independence from highly varying water discharge, e.g.,. thataccompanying severe rainstorms, indicates rapidly re-attained equilibrium.Variations in the concentrations of cations are likely due to exchange withunmeasured cations, probably H⁺ or dissolved Al species, as aresult of possible seasonal changes in internal acid production and externalinput of acid rain to the sandboxes. Internal production may represent aresponse to seasonal changes in respiration rate as it responds toseasonally varying temperature. Added to this is the effect of temperatureon exchange equilibrium. Seasonal variations in dissolved silica are mostlikely due to the dependence of adsorption/desorption equilibria ontemperature. The temperature dependence of a number of silica-consumingreactions are consistent with the measured values.