The role of overwash in the evolution of mixing zone morphology within barrier islands

Overwash is a major controlling factor in the morphology of the mixing zone of coastal aquifers. Conceptual models of the mixing zone describe an interface controlled by tidal oscillations, wave run-up, and other factors; however, few describe the influence of large storm events. In August 1993, Hatteras Island, North Carolina, USA, experienced a 3-m storm surge due to Hurricane Emily. Sound-side flooding infiltrated a wellfield, causing a dramatic increase in TDS levels that persisted for more than 3 years. Two-dimensional simulations with SUTRA, the USGS finite-element model, are calibrated to the TDS breakthrough data of this storm to infer model dispersivity values. Simulations using the calibrated dispersivity values, predicted flooding levels, and 54 years of hurricane records to determine the influence of the overwash events suggest that it is rare for the mixing zone to approximate the conceptual morphology. Even during quiescent periods such as between 1965 and 1975, TDS levels do not return to theoretical levels before being elevated by a subsequent storm event. Thus, while tidal oscillations and other factors are important to mixing zone development, basic wind events and more severe storm events may have more influence and lasting effect on the morphology of the mixing zone.     

Evaluating the mobility of137Cs,239+240Pu and210Pb from their distributions in laminated lake sediments

Post-depositional mobility of¹³⁷Cs,^239+240Pu and²¹⁰Pb was assessed in six small lake basins by comparing sedimentary nuclide profiles with their known fallout history. Laminae couplets, when present, were determined to be varves because the¹³⁷Cs and^239+240Pu 1963 fallout peaks are present in laminae couplets corresponding to years 1962–1964. There is no evidence of mobility of²¹⁰Pb, because 1) mass accumulation rates based on²¹⁰Pb agree with those based on¹³⁷Cs and^239+240Pu peak depths and with those based on varve counts, and 2)²¹⁰Pb ages agree with varve ages. Significant mobility of¹³⁷Cs is evident from the penetration of¹³⁷Cs to depths 15–20 cm deeper than^239+240Pu. Deep penetration of¹³⁷Cs in spite of a sharp gradient below the peak is interpreted by a numerical model to suggest that¹³⁷Cs is present in two distinct forms in these sediments, 67–82% as an immobile form and 18–33% reversibly adsorbed with a K _d of approximately 5000. The profiles can be interpreted equally well assuming a small portionof the total¹³⁷Cs was present as an extremely mobile phase (K _d 5000) in the months to years following peak fallout, slowly becoming more strongly adsorbed. High NH ₄ ⁺ concentrations in porewaters may enhance diffusion of the mobile form of¹³⁷Cs, but not of the immobile form of¹³⁷Cs that defines the sharp gradient. Mobility of¹³⁷Cs is likely also enhanced by the low clay content and the high porosity of these sediments. Thus the first detection of¹³⁷Cs in the sediments cannot automatically be assumed to correspond to a date of 1952 (initial testing of thermonuclear weapons), although the depth of the peak can be assumed to correspond to 1963 (the year of maximum fallout from testing of thermonuclear weapons).^239+240Pu is a more reliable sediment chronometer than¹³⁷Cs because it is significantly less mobile.This is the sixth of a series of papers to be published by this journal following the 20 ^th anniversary of the first application of²¹⁰Pb dating of lake sediments. Dr P.G. Appleby is guest editing this series.     

Earth and Venus: A comparative study

The observed density of Venus is about 2% smaller than would be expected if Venus were a twin planet of the Earth, possessing an identical internal composition and structure. In principle, this could be explained by a process of physical segregation of metal particles from silicate particles in the solar nebula prior to accretion, so that Venus accreted from relatively metal-depleted material. However, this model encounters severe difficulties in explaining the nature of the physical segregation process and also the detailed chemical composition of the Earth's mantle. Two alternative hypotheses are examined, both of which attempt to explain the density difference in terms of chemical fractionation processes. Both of these hypotheses assume that the relative abundances of the major elements Fe, Si, Mg, Al, and Ca are similar in both planets. According to the first hypothesis, a larger proportion of the total iron in Venus is present as iron oxide in the mantle, so that the core-to-mantle ratio is smaller than in the Earth. This model implies that Venus is more oxidized than the Earth, with its lower intrinsic density (i.e., corrected to equivalent pressures and temperatures) due to the larger amount of oxygen present. The difference between oxidation states is attributed to differing degrees of accretional heating arising from the relatively smaller mass of Venus. On the other hand, the second hypothesis maintains that Venus is more reduced than the Earth, with its mantle essentially devoid of oxidized iron. The difference intrinsic densities is attributed to the Earth accreting at a lower temperature than Venus as a result of the Earth's greater distance from the center of the nebula. As a result, large amounts of sulfur accreted on the Earth but not on Venus. The sulfur, which entered the core, is believed to have increased the mean density of the Earth because of its relatively high atomic weight. The hypothesis also implies that most of the Earth's potassium, because of its chalcophile properties, entered the core.These hypotheses are evaluated in the light of existing data. The second hypothesis leads to an intrinsic density for Venus which is only 0.4% smaller than that of the Earth. This difference is much smaller than is believed to exist. A wide range of chemical evidence is found to be unfavorable to this second hypothesis, but to be consistent with the interpretation that Venus is more oxidized than the Earth, as required by the first hypothesis.     

Stable isotope (O and C) and pollen trends in eastern Lake Erie,evidence for a locally-induced climatic reversal of Younger Dryas age in the Great Lakes basin

A cool period from about 11000 to 10 500 BP (11 to 10.5 ka) is recognized in pollen records from the southern Great Lakes area by the return of Picea and Abies dominance and by the persistence of herbs. The area of cooling appears centred on the Upper Great Lakes. A high-resolution record (ca. 9 mm/y) from a borehole in eastern Lake Erie reveals, in the same time interval, this pollen anomaly, isotope evidence of meltwater presence (a — 3 per mil shift in ¹⁸O and a +1.1 per mil shift in ¹³C), increased sand, and reduced detrital calcite content, all suggesting concurrent cooling of Lake Erie. The onset of cooling is mainly attributed to the effect of enhanced meltwater inflow on the relatively large upstream Main Lake Algonquin during the first eastward discharge of glacial Lake Agassiz. Termination of the cooling coincides with drainage of Lake Algonquin, and is attributed to loss of its cooling effectiveness associated with a substantial reduction in its surface area. It is hypothesized that the cold extra inflow effectively prolonged the seasonal presence of lake ice and the period of spring overturn in Lake Algonquin. The deep mixing would have greatly increased the thermal conductive capacity of this extensive lake, causing suppression of summer surface lakewater temperatures and reduction of onshore growing-degree days. Alternatively, a rapid flow of meltwater, buoyed on sediment-charged (denser) lakewater, may have kept the lake surface cold in summer. Other factors such as wind-shifted pollen deposition and possible effects from the Younger Dryas North Atlantic cooling could have contributed to the Great Lakes climatic reversal, but further studies are needed to resolve their relative significance.Contribution to Climo Locarno — Past and Present Climate Dynamics; Conference September 1990, Swiss Academy of Sciences — National Climate ProgramGeological Survey of Canada Contribution 58 890     

Water vapor adsorption by sodium montmorillonite at −5°C

A large amount of interest has recently been expressed pertaining to the quantity of physically adsorbed water by the Martian regolith. Thermodynamic calculations based on experimentally determined adsorption and desorption isotherms and extrapolated to subzero temperatures indicate that physical adsorption of more than one or two monomolecular layers is highly unlikely under Martian conditions. Any additional water would find ice to be the state of lowest energy and therefore the most stable form. To test the validity of the thermodynamic calculations we have measured adsorption and desorption isotherms of sodium montmorillonite at ?5°C. To a first approximation it was found to be valid.     

A highlight of environmental and engineering geology in Fargo, North Dakota, USA

Several unfavorable environmental and engineering geologic conditions exist in Fargo, North Dakota. Dominantly, the behavior of smectitic clays within the proglacial Lake Agassiz sediments of the Sherack and Brenna Formations creates subsoil instability beneath engineered structures in the Fargo area and slope instability within cutbank meanders of the Red River of the North. Unfavorable engineering geologic conditions encountered include: the elastic deformation of clayey glaciolacustrine soils, shrink-swell properties, inadequate bearing capacities, and mass movements. These conditions are responsible for structural failures including the Fargo Grain Elevator in 1955 and the Northern Pacific railroad grade. Bank failures along the Red River are common due to the inherent instability of Brenna Formation smectitic clays which are subject to plastic deformation in the subsurface, with resultant block failure of overlying Sherack Formation. Recent alluvial sediments due to typical fluvial action and the continued seasonal saturation of cutbank meanders within the floodplain also add to soil instability.