Steady, annual, and monthly recharge implied by deep unconfined aquifer flow

We consider the response of a deep unconfined horizontal aquifer to steady, annual, and monthly recharge. A groundwater divide and a zero head reservoir constrain the aquifer, so that sinusoidal monthly and aperiodic annual recharge fluctuations create transient specific discharge near the reservoir and an unsteady water table elevation inland. One existing and two new long-term data sets from the Plymouth-Carver Aquifer in southeastern Massachusetts calibrate and confirm hydraulic properties in a set of analytical models. [Geohydrology and simulated groundwater flow, 1992] data and a new power law for tritiugenic helium to tritium ratios calibrate the steady recharge that drives the classical parabolic model of steady hydraulics [Applied Hydrogeology, 2001]. Observed water table and gradient fluctuations calibrate the transient recharge models. In the latter regard, monitoring wells within 1 km of Buttermilk Bay exhibit appreciable specific discharge and reduced water table fluctuations. We apply [Trans Am Geophys Union 32(1951)238] periodic model to the monthly hydraulics and a recharge convolution integral [J Hydrol 126(1991)315] to annual flow. An infiltration fraction of 0.79 and a consumptive use coefficient of 1.08×10⁻⁸ m/s °C relate recharge to precipitation and daylight weighted temperature across all three time scales. Errors associated with this recharge relation decrease with increasing time scale.     

Similarities between strike-slip faults at different scales and a simple age determining method for active faults

Abstract Several differently scaled strike‐slip faults were examined. The faults shared many geometric features, such as secondary fractures and linkage structures (damage zones). Differences in fault style were not related to specific scale ranges. However, it was recognized that differences in style may occur in different tectonic settings (e.g. dilational/contractional relays or wall/linkage/tip zones), different locations along the master fault or different fault evolution stages. Fractal dimensions were compared for two faults (Gozo and San Andreas), which supports the idea of self‐similarity. Fractal dimensions for traces of faults and fractures of damage zones were higher (D ～1.35) than for the main fault traces (D ～1.005) because of increased complexity due to secondary faults and fractures. Based on the statistical analysis of another fault evolution study, single event movements in earthquake faults typically have a maximum earthquake slip : rupture length ratio of approximately 10^?4, although this has only been established for large earthquake faults because of limited data. Most geological faults have a much higher maximum cumulative displacement : fault length ratio; that is, approximately 10^?2 to 10^?1 (e.g. Gozo, ～10^?2; San Andreas, ～10^?1). The final cumulative displacement on a fault is produced by accumulation of slip along ruptures. Hence, using the available information from earthquake faults, such as earthquake slip, recurrence interval, maximum cumulative displacement and fault length, the approximate age of active faults can be estimated. The lower limit of estimated active fault age is expressed with maximum cumulative displacement, earthquake slip and recurrence interval as T ? (d_max /u) · I(M).     

The most energetic particles

The 3rd International Workshop on Ultra High Energy Cosmic Rays covered such topics as results from experiments, theory and models, and the links with γ-rays, neutrinos, dark matter and the cosmic microwave background radiation. David Newton reports.     

Vertical Delineation of Contamination in Fractured Bedrock Aquifer

The New Jersey Department of Environmental Protection's Technical Regulations require the horizontal and vertical delineation of contamination. Monitor wells screened at increasingly deeper intervals are used to delineate vertical contamination. In New Jersey, the open interval in a bedrock well cannot exceed 7.6 m. Since contamination has been found at depths as great as 91.4 m in a production well in the study area, it would be prohibitively expensive to install monitor wells with 7.6 m open holes at ever-increasing depths until no contamination was found. Isolation of discrete zones in boreholes using pneumatic packers was implemented at a site in north central New Jersey. Ground water samples were collected from selected 6.1 m sections of boreholes drilled into fractured bedrock at three locations on the property and one offsite location. The ground water samples were analyzed in a field laboratory. The analytical results were used to determine the vertical extent of gasoline-related compounds dissolved in the ground water on the property and offsite. These compounds include benzene, ethylbenzene, methyl tertiary butyl ether, toluene, and xylenes. The four boreholes were converted into bedrock monitor wells. The intake interval for each of the wells was selected through evaluation of the vertical distribution of contaminants as determined from analytical results obtained from a field laboratory located onsite. Three wells are used for the recovery of contaminated ground water. The recovered water will be treated at the onsite air-stripping unit. The fourth well is used to chemically and hydraulically monitor the progress of the ground water recovery program.     

Web-cam’s potential for collaborative activities in the Earth sciences

We report here our experiences from using easily acquired web-cam components for collaborative ventures in the Earth sciences. We have used a variety of hardware and different software. We demonstrate from various locations in the U.S.A. the feasibility of using web-cam in multitudinous activities, relevant for conducting research and knowledge dissemination. We summarize the quality of the connections from the various combinations of communicating parties. Today, web-cams can be utilized as an economical and viable means of point-to-point communication in the Earth science community. Greater bandwidth is sorely needed for activities such as multi-party conferencing on the present internet network. We propose that web-cam can be readily deployed as a web-service for facilitating collaborative research over the GRID infrastructure, using the middleware Narada-Brokering. Web-cam will play an important role in the emerging field of geoinformatics.     

Importance of mantle derived fluids during granite associated hydrothermal circulation: He and Ar isotopes of ore minerals from Panasqueira

Helium trapped in arsenopyrite and wolframite from the Panasqueira hydrothermal deposit in central Portugal is overwhelmingly—≈ 75%—derived from the mantle. This is surprising as the W-Cu(Ag)-Sn vein deposits are spatially and temporally associated with an S-type granite. It is difficult to reconcile ³He/⁴He ratios > 5Ra (where Ra is the atmospheric ³He/⁴He ratio) with a granite produced by crustal anatexis, therefore it seems likely that mantle derived fluids unrelated to the granite were the source of the magmatic component in the ore fluids.The mantle appears to transport ³He and heat to the surface in relatively constant proportions (³He/Q = 0.1-1 x10⁻¹² cm³ STP J⁻¹). However, the ³He/heat ratios in the Panasqueira fluids (1-10 x10⁻¹² cm³ STP J⁻¹, calculated using the ³He/³⁶Ar ratio) are considerably higher. Therefore, it does not seem likely that gradual cooling of the pluton supplied heat to the hydrothermal system (as this would result in low ³He/Q ratios). Therefore, both He and heat in this collision related, granite-associated hydrothermal deposit were supplied from the mantle.     

An experimental and theoretical determination of oxygen isotope fractionation in the system magnetite-H2O from 300 to 800°C

Oxygen isotope fractionations have been determined between magnetite and water from 300 to 800°C and pressures between 10 and 215MPa. We selected three reaction pathways to investigate fractionation: (a) reaction of fine-grained magnetite with dilute aqueous NaCl solutions; (b) reduction of fine-grained hematite through reaction with dilute acetic acid; and (c) oxidation of fine iron power in either pure water or dilute NaCl solutions. Effective use of acetic acid was limited to temperatures up to about 400°C, whereas oxide-solution isotope exchange experiments were conducted at all temperatures. Equilibrium ¹⁸O/¹⁶O fractionation factors were calculated from the oxide-water experiments by means of the partial isotope exchange method, where generally four isotopically different waters were used at any given temperature. Each run product was characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), and on a limited basis, high-resolution transmission electron microscopy (HRTEM) and Mössbauer spectroscopy. Results from the microscopic examinations indicate the formation of well-crystallized octahedra and dodecahedra of magnetite where the extent of crystallization, grain size, and grain habit depend on the initial starting material, P, T, solution composition, and duration of the run.The greatest amount of oxygen isotope exchange (∼90% or greater) was observed in experiments where magnetite either recrystallized in the presence of 0.5 m NaCl from 500 to 800°C or formed from hematite reacted with 0.5 m acetic acid at 300, 350 and 400°C. Fractionation factors (10³ ln α_mt-H2O) determined from these partial exchange experiments exhibit a steep decrease (to more negative values) with decreasing temperature down to about 500°C, followed by shallower slope. A least-squares regression model of these partial exchange data, which accounts for analytical errors and errors generated by mass balance calculations, gives the following expression for fractionation that exhibits no minimum: 1000lnα_lmt-lw=−8.984(±0.3803)x+3.302(±0.377)x²—0.426(±0.092)x³ with an R² = 0.99 for 300 ≤ T≤ 800°C (x = 10⁶/T²). The Fe oxidation results also exhibit this type of temperature dependence but shifted to slightly more negative 10³ ln α values; there is the suggestion that a kinetic isotope effect may contribute to these fractionations. A theoretical assessment of oxygen isotope fractionation using β-factors derived from heat capacity and Mössbauer temperature (second-order Doppler) shift measurements combined with known β-factors for pure water yield fractionations that are somewhat more negative compared to those determined experimentally. This deviation may be due to the combined solute effects of dissolved magnetite plus NaCl (aq), as well as an underestimation of β_mt at low temperatures. The new magnetite-water experimental fractionations agree reasonably well with results reported from other experimental studies for temperatures ≥ 500°C, but differ significantly with estimates based on quasi-theoretical and empirical approaches. Calcite-magnetite and quartz-magnetite fractionation factors estimated from the combination of magnetite β’s calculated in this study with those for calcite and quartz reported by Clayton and Kieffer (1991) agree very closely with experimentally determined mineral-pair fractionations.     

Macroscale NTIMS and microscale LA-MC-ICP-MS Re-Os isotopic analysis of molybdenite: Testing spatial restrictions for reliable Re-Os age determinations, and implications for the decoupling of Re and Os within molybdenite

We present a detailed study of Re-Os age determinations for eight natural molybdenite samples of like polytype (2H), spanning a range of age, natural grain size and deposit type. The focus of the study is to critically evaluate the effects of sampling, sample preparation and aliquant size on the accuracy and reproducibility of Re-Os ages for these molybdenite samples. We find that for some molybdenite samples, analysis of small sample aliquants (<20 mg) may not yield accurate or reproducible Re-Os ages, whereas analysis of larger aliquants from the same mineral separate do yield reproducible Re-Os dates. Such an observation is best explained if Re and ¹⁸⁷Os are internally decoupled within molybdenite grains. This finding is supported from spot analyses by laser ablation MC-ICP-MS analyses presented here and is consistent with previously published observations.The degree of decoupling between Re and ¹⁸⁷Os appears to increase both as a function of increasing grain size, and increasing age of molybdenite. From detailed dating of individual molybdenite mineral separates, we provide approximate minimum aliquant amounts required for reproducible Re-Os age dating, as a function of molybdenite age and grain size. Geologically younger, naturally fine-grained molybdenite samples appear to show little Re and ¹⁸⁷Os decoupling, and reproducible ages can be determined from some samples with as little as 1 mg of aliquant. Geologically old, and coarse-grained molybdenite samples may require as much as 40 mg of aliquant from a much larger mineral separate to overcome Re and ¹⁸⁷Os decoupling. The mechanism(s) of Re and ¹⁸⁷Os decoupling within molybdenite is not constrained by this results of this study, but the observation that the degree of decoupling increases with grain size (distance) and age (time/geologic history) may suggest primary diffusive control. Assuming that Re and ¹⁸⁷Os decoupling in molybdenite results primarily from diffusion of ¹⁸⁷Os, apparent diffusion coefficients are calculated (D = x²/t). Estimates of D for Os made in this way range from 2.8 × 10⁻²⁶ to 2.1 × 10⁻²¹ m²/s, which are broadly similar to experimentally derived diffusion coefficients for Os in Fe-sulfide minerals and for Re in molybdenite at temperatures <500°C.