ALBERT

Notes: Abstract. An effective fertilizer recommendation system requires information on seasonal, soil-related and cultural variations in soil mineral nitrogen (N) and nutrient requirements of the crop. This can be provided by dynamic N turnover models, such as listed by Plentinger & Penning De Vries (1996). In this paper, we describe a survey of farmer opinion designed to ascertain what farmers want from such a decision support system. Over 100 farmers were surveyed. Surveyed farmers requested that default values be available for all model inputs. Inputs should be entered both by windows-based menu (for clarity) and tabular format (for speed), have user-selected units, and be fully supported by context-sensitive help. The system should have a hierarchical structure allowing access to fixed parameters, and be compatible with commonly used farm recording packages. Recommendations should be provided both for the field (single and optional application rates), and in tabular format across the whole farm. Simulations should be easily rerun using more recent crop and weather data. Turnover processes underlying recommendations should be illustrated by flow diagrams of flux between pools, pie charts of fertilizer fate, bar charts of movement down the soil profile and graphical plots of changes in N status against time.

Notes: A spill of JP-4 jet fuel at the U.S. Coast Guard Air Station in Traverse City, Michigan, contaminated a water-table aquifer. An infiltration gallery (30 ft × 30 ft) was installed above a section of the aquifer containing 700 gal JP-4. Purge wells recirculated three million gallons of ground water per week through the infiltration gallery at a rate designed to raise the water table above the contaminated interval. Ground water containing ambient concentrations of oxygen and nitrate was first recirculated for 40 days. Concentrations of benzene in monitoring wells beneath the infiltration gallery were reduced from 760 to 〈1μ/1. Concentrations of toluene, ethylbenzene, m,p-xylene, and o-xylene were reduced from 4500 to 17, 840 to 44, 2600 to 490, and 1400 to 260 μ/1, respectively. Average core concentrations of benzene, toluene, ethylbenzene, m,p-xylene, and o-xylene were reduced from 0.84 to 0.032, 33 to 0.13, 18 to 0.36, 58 to 7.4, and 26 to 3.2 mg/kg, respectively. Ground water amended with nitrate (10 mg/1 nitrate-nitrogen) and nutrients was then recirculated for 76 days. Final core concentrations of benzene, toluene, ethylbenzene, m,p-xylene, and o-xylene were 0.017,0.036,0.019,0.059, and 0.27 mg/kg, respectively. Final aqueous concentrations were 〈1 μ/1 for benzene and toluene, 6 μ/1 for ethylbenzene, and 20 to 40 μ/1 for the xylene isomers, in good agreement with predicted values based on residual fuel content and partitioning theory. Although alkylbenzene concentrations have been substantially reduced, the test plot is still contaminated with the weatheredfuel. Based on stoichiometry, approximately 10 times more nitrate was consumed than could be accounted for by BTX degradation alone, indicating that other compounds were also degraded under denitrifying conditions.

Notes: A six-channel wide-band digital system for magnetotelluric measurements is described The system is designed to operate in the frequency band 10-.0001 Hz. The recording is made on a 7 track tape in an IBM compatible 12 bit format. The amplitude and phase responses of the system and sample records are presented.

Notes: The ability to predict the transport of dissolved gases in the presence of small amounts of trapped gas in an otherwise water-saturated porous medium is needed for a variety of applications. However, an existing model based on equilibrium partitioning of dissolved gas between aqueous and trapped gas phases does not accurately predict the shape of experimentally observed breakthrough and elution curves in column experiments. The objective of this study was to develop and test a kinetic model for dissolved gas transport that combines the advection-dispersion equation with diffusion controlled mass transfer of dissolved gas between the aqueous and trapped gas phases. The model assumes one-dimensional, steady-state ground-water flow, a single dissolved gas component, and a stationary trapped gas phase with constant volume. The model contains three independent parameters: the Peclet number, P, retardation factor, R, and dimensionless mass transfer parameter, ω. The model accurately described the shape of breakthrough and elution curves for dissolved oxygen in column experiments performed with a poorly graded sand and varying amount and composition of trapped gas. Estimated values of P for the bromide tracer increased from 5.92 to 174, corresponding to a decrease in dispersivity from 5.02 to 0.17 cm, as the trapped gas volume increased from 0 to 30% of the pore space. It is speculated that this effect is due to a narrower pore size distribution (and hence more uniform pore scale velocity distribution) caused by trapped gas bubbles selectively occupying the largest pores. Estimated values of R increased from 1 to 13.6 as the trapped gas volume increased and confirmed earlier observations that even small amounts of trapped gas can significantly reduce rates of dissolved oxygen transport. Estimated values of ω ranged from 0.3 to 12.1. Although it was not possible to independently measure mass transfer coefficients or interfacial areas, values computed from flow rates and estimated w values are consistent with values computed by assuming (1) that interfacial area is proportional to trapped gas volume, (2) that trapped gas bubbles are spheres with diameters the same size as soil particles, and (3) that mass transfer is limited by diffusion of dissolved oxygen through water films surrounding trapped gas bubbles.

Notes: Observations of the threshold of movement of loosely packed gravel in a tidal current are described. For gravel with equivalent ‘spherical’ diameters D in the range 0.2 ≲D≲ 5.0cm the critical friction velocity u*c, corresponding to the initiation of sediment transport, is given by u*c=7.0 D0.2. At large values of D within the quoted range, the value u*c is significantly lower than would be obtained by a Shields experiment (u*c∞D0.5). By comparing our values of u*c with those obtained under well-controlled laboratory conditions, the discrepancy with Shields is shown to be due to the open spacing between, and exposure of, individual pebbles on the seabed. By comparing our results with those from upland gravel streams and flume experiments, it is suggested that Shields assumed an excessively large water depth to particle size ratio as a constraint within which the critical sediment entrainment number 0c is valid.

Notes: Abstract Archaean greenstone belts are often cut by major shear zones, for example the Cadillac tectonic zone (CTZ) of the southern Abitibi region in north-western Quebec. At McWatters, the CTZ contains slices of metavolcanic units bounded by corridors of highly strained and altered rocks. Mineral assemblages of the metabasites record the metamorphic evolution of the CTZ.The McWatters metabasalts and metagabbros have similar chemistry but different mineral assemblages consisting of variable amounts of actinolite, hornblende, chlorite, albite, epidote, quartz, carbonates, titanite, biotite, rutile, magnetite, ilmenite and sulphides. The different mineral assemblages, which coexist in a single tectonic slice, can be divided into three types, characterized by (A) presence of hornblende and actinolite, (B) presence of actinolite and epidote, and (C) absence of amphibole and epidote. Partial replacements indicate that these mineral assemblages are not in equilibrium. The hornblende of the least altered and deformed samples of the type A assemblage is a relict of a prograde metamorphic event, contemporaneous with the development of the main schistosity. The prograde conditions are estimated at P= 5 kbar, T= 475° C with low Pf. The more altered and deformed samples of the type C assemblage record a later retrograde metamorphic event. Conditions of the later event are estimated at P= 4 kbar, T= 400° C with higher Pf. Widespread calcite precipitation occurred during a later episode. The diversity of the mineral assemblages results from permeability variations along the high-strain zones of the CTZ.

Notes: Olivine-plagioclase coronas in metagabbros from the Adirondack Mountains, New York (USA) are spatially well-organized reaction textures consisting most commonly of sequential layers of orthopyroxene, clinopyroxene, plagioclase, and garnet; the textures are characteristic of diffusion-controlled reaction kinetics. Although similar coronas have been interpreted by previous workers in terms of an isochemical steady-state diffusion model, petrographical relations and material-balance calculations establish that coronas in the Adirondack metagabbros cannot be treated as isochemical and do not form in a single-stage steady-state process; instead they evolve through time in a complex open-system reaction.In this study, the isochemical diffusion model is modified to account for elemental fluxes across the outer boundaries of the coronal reaction band, thereby approximating the open-system behaviour of the coronas. The sequence and relative proportions of product minerals calculated by the open-system steady-state model correspond closely to those observed in coronas of the Adirondacks, over a wide range of values for the relative diffusivities of chemical components involved in the reaction, regardless of the particular method used to determine material balance in the reaction texture.Despite this correspondence, petrographical evidence for successive replacement of coronal product layers reveals that the Adirondack coronas evolved through one or more transient states, rather than forming in a single-stage steady-state process. There is no evidence that the successive replacement of coronal product layers resulted from changes in pressure or temperature, but there is petrographical evidence that these changes resulted from modification of the composition of reactant plagioclase as the corona-forming reaction proceeded. This is confirmed by the fact that the evolution of the coronas over time can be replicated with the open-system diffusion model by simulating the effect of the gradual exhaustion of plagioclase as a source of the Ca and Si components required for reaction. These simulations suggest that successive stages in the evolution of the coronas are characterized by these product sequences: (i) orthopyroxene-clinopyroxene-plagioclase-garnet; (ii) orthopyroxene-clinopyroxene-garnet; and (iii) orthopyroxene-garnet. All of these stages, and the transitions between them, are observed petrographically. Coronas in Adirondack metagabbros appear, therefore, to have originated in a complex, open-system, diffusion-controlled reaction in which the product assemblages changed as the reaction progressed.

Notes: The alkalic Scituate Granite was emplaced into crystalline sequences within the New England Esmond–Dedham terrane in the Late Devonian (c. 370 Ma). Variably recrystallized amphibole (iron-rich, hastingsite–hastingsitic hornblende) from four variably deformed samples of the pluton record south-westerly younging 40Ar/39Ar plateau ages ranging between 276 and 263 Ma. These are interpreted to date diachronous cooling through temperatures appropriate for intracrystalline retention of argon following late Palaeozoic orogenic activity. Iron-rich biotite concentrates from the samples record only slightly younger ages, and therefore suggest relatively rapid post-metamorphic cooling. The 40Ar/39Ar ages indicate that the late Palaeozoic tectonothermal overprint was much more regionally pervasive than was previously considered. The apparent timing of this activity is similar to previous estimates for the chronology of high-grade metamorphism throughout the adjacent Hope Valley terrane and for phases of ductile movement on the intervening Lake Char–Honey Hill fault system.

Notes: Incipient metamorphism accompanying thrusting, folding and cleavage development has been investigated in a varied sequence of Palaeozoic sediments near the Variscan front in SW Dyfed, Wales. The aim was to evaluate a critical stage in the progression from heterogeneous sediment, whose detrital phases are neither in equilibrium with one another, nor with pore fluids, through indurated sedimentary rock to metamorphic rock comprising newly formed crystals that equilibrated with one another as they grew.Quartz veins are widely developed in the area, especially in the more psammitic lithologies, while finer grained rocks became cleaved during tectonic deformation. Mineralogical constraints and fluid inclusion measurements suggest maximum temperatures around 200-310d̀ C (slightly higher in the Marloes-Musselwick Thrust Sheet than in other parts of the structural succession) at depths of the order of 6-13 km.Quartz veins yield distinctly heavier oxygen isotopic compositions than detrital quartz grains in the adjacent wall rocks, although care must be taken in interpreting the data because slivers of detrital grains may become incorporated into veins, while matrix detrital grains may incorporate veinlets or rims of newly formed quartz. It is concluded that vein quartz grew in isotopic equilibrium with a fluid phase whose isotopic composition was primarily controlled by exchange with phyllosilicates, not detrital quartz grains. Vein and matrix quartzes from the Marloes-Musselwick Thrust Sheet are distinctly lighter (δ18Oveins=+14 to +18% and δ18Omatrix=+11 to +14%) than those from other thrust sheets (δ18O =+17 to +20% and +14 to +17%, respectively).We conclude that vein quartz and phyllosilicate grains in cleavage domains probably attained equilibrium with a locally buffered pore fluid at the peak of metamorphism, but many relict grains of different chemical and isotopic composition remained elsewhere in the rock. Local fluid migration along veins and through cleavage lamellae facilitated the attainment of equilibrium, but there is little evidence for large-scale infiltration of externally derived fluids. With further metamorphism the quartz in these rocks would attain an isotopic composition intermediate between that of the heavy vein material and light detritus which coexist here.