The formation and detection of metal dispersion halos in organic lake sediments

The application of organic-rich lake sediment (gyttja) to exploration geochemistry is discussed. Gyttja was collected from some 42 lake sites in the Red Lake-Uchi Lake volcanic-sedimentary sequences.The existance of free sulphide ion in most gyttja is confirmed and theoretical calculations are used to define the approximate concentrations of sulphide ion which determine whether the accumulation of Cu⁺, Cu²⁺, Zn²⁺ and Fe²⁺ is by metal sulphide precipitation, organic complexing or both. These calculations show that in the sediments collected in this study, the accumulation of copper will probably be by metal sulphide formation, whereas for zinc, organic complexing and possibly sulphide precipitation are likely mechanisms.It is shown that the background concentrations of copper and zinc on a dry matter basis increase with the content of organic matter in the sediment and it is further shown that the quantity of interstitial water in the sediment increases linearly with the organic content. Also it is demonstrated that the organic matter in the sediment is dispersed in the interstitial water in approximately the same concentration irrespective of the sediment composition.On the assumption that copper sulphide colloids are dispersed in the interstitial water of the sediment, it is suggested that the copper content of gyttja should be expressed as μg/g interstitial water for meaningful interpretation. Similarly, the zinc content should be expressed relative to the organic matter content.The ability of reagents to selectively extract only chemically dispersed metals and not silicate lattice metals from gyttja is discussed.Both the analytical procedures and the interpretations are applied to the samples collected.     

Accuracy of CFC groundwater dating in a crystalline bedrock aquifer: Data from a site in southern Sweden

The concentrations of chlorofluorocarbons (CFC-11, CFC-12, and CFC-113) and tritium were determined in groundwater in fractured crystalline bedrock at Finnsjön, Sweden. The specific goal was to investigate the accuracy of CFC dating in such an environment, taking potential degradation and mixing of water into consideration. The water was sampled to a depth of 42 m in three boreholes along an 800-m transect, from a recharge area to a local discharge area. The CFC-113 concentration was at the detection limit in most samples. The apparent recharge date obtained from CFC-11 was earlier than from CFC-12 for all samples, with a difference of over 20 years for some samples. The difference was probably caused by degradation of CFC-11. The CFC-12 dating of the samples ranged from before 1945 to 1975, with the exception of a sample from the water table, which had a present-day concentration. Conclusions about flow paths or groundwater velocity could not be drawn from the CFCs. The comparison between CFC-12 and tritium concentrations showed that most samples could be unmixed or mixtures of waters with different ages, and the binary mixtures that matched the measured concentrations were determined. The mixing model approach can be extended with additional tracers.

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Resumen Precisión en la datación de aguas subterráneas utilizando CFC en un acuífero de rocas cristalinas: datos provenientes de un sitio al sur de Suecia.Se determinaron las concentraciones de clorofluorucarbonos (CFC-11, CFC-12, y CFC-113) y de tritio en aguas subterráneas alojadas en rocas cristalinas fracturadas de Finnsjön, Suecia. El objetivo específico consistió en investigar la precisión de la datación de aguas subterráneas con CFC en este tipo de ambiente, tomando en consideración la degradación potencial y la mezcla de agua. Las muestras de agua se tomaron a una profundidad de 42 m en tres pozos ubicados a lo largo de una línea de 800 m transversal a una zona de recarga y de zona de descarga local. En la mayoría de las muestras se encontró que la concentración de CFC-113 estuvo en el límite de detección. La edad que se estimó en todas las muestras para la recarga aparente en base a CFC-11 fue más joven que la edad proveniente de CFC-12, con una diferencia de más de 20 años para algunas muestras. Esta diferencia fue causada probablemente por la degradación del CFC-11. La datación CFC-12 de las muestras varió de antes de 1945 a 1975, con la excepción de una muestra tomada en el nivel freático, la cual presentó concentración actual. No fue posible obtener conclusiones acerca de las trayectorias de flujo o la velocidad de agua subterránea a partir de los CFCs. La comparación entre las concentraciones de CFC-12 y tritio mostró que la mayoría de las muestras pueden tener composición sencilla o bien consistir de mezclas de aguas de diferentes edades. Esta comparación también permitió determinar las mezclas binarias que corresponden a las concentraciones medidas. Pueden utilizarse trazadores adicionales para ampliar el modelo de mezclas propuesto.

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Résumé Précision de la datation au CFC dans un aquifère rocheux-fracturé: données dun site du sud de la Suède.Les concentrations en chlorofluorocarbones (CFC-11, CFC-12, CFC-113) et entritium ont été déterminées dans leau souterraine dun massif fracturé à Finnsjön en Suède. Le but de cette étude est de mieux cerner la précision de la méthode de datation au CFC dans ce type denvironnement hydrogéologique, tout en considérant déventuels phénomènes de dégradation et de mélange deaux. Leau a été échantillonnée à une profondeur de 42 mètres dans trois forages alignés sur 800 mètres entre une zone de recharge et une zone de déversement. Les concentrations en CFC-113 sont dans la plupart des échantillons à la limite de détection. Pour tous les échantillons, la date de la recharge établie avec le CFC-11 est antérieure à la date établie avec le CFC-12. La différence entre les deux dates peut dépasser 20 ans et sexplique—probablement—par la dégradation du CFC-11. Les dates de recharge de la nappe mesurées au CFC-12 sont comprises entre 1945 et 1975, excepté pour un échantillon qui possède une concentration actuelle. Il nest pas possible de tirer des conclusions concernant la direction des écoulements et la vitesse de leau souterraine. La comparaison entre CFC-12 et tritium montre que des échantillons pourraient être soit le résultat du mélange deaux dâges différents, soit des échantillons non-mélangés. Dans le cas dun mélange binaire, les rapports du mélange composant la concentration mesurée sont déterminés. Lapproche par modèle de mélange peut être étendue à des traceurs additionnels.

     

ULF pulsation mode coupling in the ionosphere and magnetosphere

The effect of realistic ionospheric Hall conductances on axisymmetric toroidal mode hydromagnetic wave resonances is investigated. The toroidal modes couple to evanescent poloidal modes near the ionospheres such that the composite modes resonate at the constant frequencies of the corresponding single-field-shell resonances for zero Hall conductance. A model for these composite modes is developed which has narrow but finite latitudinal resonance widths such as to make the modes valid solutions of the hydromagnetic equations. The modes also suggest that “shell” solutions can realistically describe such properties of real pulsations as frequency, damping, phase variation along the field-line and node-antinode behaviour at the ionospheres. Estimates of ionospheric coupling strength are obtained and compared with magnetospheric coupling strength. It is found that magnetospheric coupling dominates ionospheric coupling for any single non-axisymmetric mode. However, ionospherically coupled axisymmetric modes should be necessary components of the Fourier sum of modes required to model any real pulsation of low to moderate apparent azimuthal wave number.Estimates of the range of magnetospheric coupling strength are obtained for pulsations under a variety of conditions.     

On the diurnal period variation of midlatitude ULF pulsations

Magnetometer studies of the periods of mid-latitude ULF pulsations have produced conflicting results on the variation of the pulsation periods with both latitude and local time. Since the mid-latitude geomagnetic field is not expected to be significantly distorted by the solar wind, the observed diurnal period variations should be determined by changes in the ambient plasma density. We have applied a physically realistic plasmasphere model to the determination of pulsation eigenperiods over a 24-h interval at L=2.3 (appropriate to Wellington, New Zealand). The resulting model pulsation eigenperiods are largest during the day, with minimum and maximum values at 05.00 and 18.00 L.T. respectively. The model predicts a general increase in the eigenperiods during the replenishment of the protonosphere after a period of geomagnetic activity.     

Sulfur electronic environments in α-NiS and β-NiS: examination of the relationship between coordination number and core electron binding energies

X-ray photoelectron spectra have been obtained under the same experimental conditions for synthetic α-NiS and natural β-NiS in order to establish any difference in S electronic environment, and to test the proposition that S core electron binding energies increase measurably with coordination number when the same metal is in different sulfide structures or lattice sites. The Ni and S electronic environments in the two NiS structures have been further probed by near-edge X-ray absorption fine structure (NEXAFS) spectroscopy, and the NEXAFS spectra interpreted by reference to spectra simulated by ab initio calculations. The photoelectron and NEXAFS spectra for freshly prepared surfaces of α-NiS and β-NiS were found to be similar, with only subtle differences in electronic environment evident in the experimental and simulated NEXAFS spectra. The measured and calculated core electron binding energies did not support the previously postulated relationship between S coordination number and electron binding energies.     

Intercomparison of Formaldehyde Measurements in Clean and Polluted Atmospheres

Three different techniques used tomeasure atmospheric formaldehyde were compared duringa field campaign carried out at a clean maritime siteon the West coast of Ireland. Two spectroscopictechniques Differential Optical AbsorptionSpectroscopy (DOAS) and Tunable Diode Laser AbsorptionSpectroscopy (TDLAS), together with a glass coil/Hantzschreaction/fluorescence technique, wereemployed for measurements of atmospheric formaldehydeof the order of a few hundred pptv. The betteragreement was observed between the fluorescence andDOAS instruments.Two DOAS instruments were compared to the glasscoil/Hantzsch reaction/fluorescence technique at asemi-polluted site on the North Norfolk coast, U.K.,where concentrations of formaldehyde were observed atlevels up to 4 ppbv. A very good agreement wasobserved between the two instruments.The glass coil/Hantzsch reaction/fluorescence and theTDLAS instruments were also deployed simultaneously inorder to measure indoor air inside a mobile laboratorylocated at the Imperial College Silwood Park site nearAscot, U.K. The doors of the mobile laboratory wereleft open in order to obtain the backgroundformaldehyde concentrations. Closing them afterwardsallowed us to observe the increase in concentrationsas a result of indoor emissions. The agreement betweenthe two instruments was outstanding (correlationcoefficient was 99%).The results from this study showed that of the fourinstruments included in this intercomparison the glasscoil/Hantzsch reaction/fluorescence technique provedthe most suitable for continuous measurements offormaldehyde in the background atmosphere.     

Spreadsheet Modeling of Slug Tests Using the van der Kamp Method

Slug testing is frequently employed to calculate aquifer transmissivity and hydraulic conductivity. The van der Kamp technique for interpreting slug test data which experience force-free water level oscillations is not routinely employed because it requires adjusting equations to match the observed well response data. This adjustment can be rapid and convenient when a commercial spreadsheet is employed.     

XVth INTERNATIONAL CONGRESS OF PHOTOGRAMMETRY AND REMOTE SENSING

The XVth International Congress of Photogrammetry and Remote Sensing, organised by the International Society for Photogrammetry and Remote Sensing, was held at Rio Centro. Rio de Janeiro from 17th to 29th June, 1984. Reports on the activities of the seven technical Commissions as well as on the Exhibition and the General Assembly were given to a meeting of the Photogrammetric Society on 16th October, 1984. Papers were published in the International Archives of Photogrammetry and Remote Sensing 25.