Application of Hilbert‐like transforms for enhanced processing of full tensor magnetic gradient data

Commonly, geomagnetic prospection is performed via scalar magnetometers that measure values of the total magnetic intensity. Recent developments of superconducting quantum interference devices have led to their integration in full tensor magnetic gradiometry systems consisting of planar‐type first‐order gradiometers and magnetometers fabricated in thin‐film technology. With these systems measuring directly the magnetic gradient tensor and field vector, a significantly higher magnetic and spatial resolution of the magnetic maps is yield than those produced via conventional magnetometers. In order to preserve the high data quality in this work, we develop a workflow containing all the necessary steps for generating the gradient tensor and field vector quantities from the raw measurement data up to their integration into high­resolution, low­noise, and artefactless two‐dimensional maps of the magnetic field vector. The gradient tensor components are processed by superposition of the balanced gradiometer signals and rotation into an Earth‐centred Earth‐fixed coordinate frame. As the magnetometers have sensitivity lower than that of gradiometers and the total magnetic intensity is not directly recorded, we employ Hilbert‐like transforms, e.g., integration of the gradient tensor components or the conversion of the total magnetic intensity derived by calibrated magnetometer readings to obtain these values. This can lead to a better interpretation of the measured magnetic anomalies of the Earth's magnetic field that is possible from scalar total magnetic intensity measurements. Our conclusions are drawn from the application of these algorithms on a survey acquired in South Africa containing full tensor magnetic gradiometry data.     

Geochemistry and shock petrography of the Crow Creek Member,South Dakota,USA: Ejecta from the 74‐Ma Manson impact structure

Abstract— The Crow Creek Member is one of several marl units recognized within the Upper Cretaceous Pierre Shale Formation of eastern South Dakota and northeastern Nebraska, but it is the only unit that contains shock‐metamorphosed minerals. The shocked minerals represent impact ejecta from the 74‐Ma Manson impact structure (MIS). This study was aimed at determining the bulk chemical compositions and analysis of planar deformation features (PDFs) of shocked quartz; for the basal and marly units of the Crow Creek Member. We studied samples from the Gregory 84‐21 core, Iroquois core and Wakonda lime quarry. Contents of siderophile elements are generally high, but due to uncertainties in the determination of Ir and uncertainties in compositional sources for Cr, Co, and Ni, we could not confirm an extraterrestrial component in the Crow Creek Member. We recovered several shocked quartz grains from basal‐unit samples, mainly from the Gregory 84‐21 core, and results of PDF measurements indicate shock pressures of at least 15 GPa. All the samples are composed chiefly of SiO₂ (29–58 wt%), Al₂O₃ (6–14 wt%), and CaO (7–30 wt%). When compared to the composition of North American Shale Composite, the samples are significantly enriched in CaO, P₂O₅, Mn, Sr, Y, U, Cr, and Ni. The contents of rare earth elements (REE), high field strength elements (HFSE), Cr, Co, Sc, and their ratios and chemical weathering trends, reflect both felsic and basic sources for the Crow Creek Member, an inference, which is consistent with the lithological compositions in the environs of the MIS. The high chemical indices of alteration and weathering (CIA' and CIW': 75–99), coupled with the Al₂O₃‐(CaO*+Na₂O)‐K₂O (A‐CN'‐K) ratios, indicate that the Crow Creek Member and source rocks had undergone high degrees of chemical weathering. The expected ejecta thicknesses at the sampled locations (409 to 219 km from Manson) were calculated to range from about 1.9 to 12.2 cm (for the present‐day crater radius of Manson), or 0.4 to 2.4 cm (for the estimated transient cavity radius). The trend agrees with the observed thicknesses of the basal unit of the Crow Creek Member, but the actually observed thicknesses are larger than the calculated ones, indicating that not all of the basal unit comprises impact ejecta.     

Assessment of massive sulphide base metal targets using lead isotopes in soils

An assessment is made of the use of lead isotopes in soils as an exploration tool for concealed lead-rich base metal massive sulphide deposits, using four case histories in southeast Australia as examples. Case history 1 covers soil profiles (< 1 m depth) unrelated to mineralization in which the lead isotope ratios exhibit variation with depth and are different from those for massive sulphide deposits. Case history 2 covers six shallow (< 0.4 m depth) profiles from two traverses over the concealed Elura Zn-Pb-Ag deposit in central western New South Wales. For one traverse over completely concealed (blind) sulphides, no isotopic or geochemical signature of the orebody could be detected. In two profiles from the other traverse, for depths of 0.15 m and 0.3–0.45 m, the lead isotopic ratios in the soils are identical with those in the ore (the target isotope ratios). Case history 3 covers two occurrences of Silurian volcanogenic Cu-Zn-Pb mineralization at the Benambra prospect in northeast Victoria. The isotopic ratios for the soils are identical with those in the sulphides and the isotopic signature of the sulphides is also detectable in traverses where no obvious surface anomaly is developed. Case history 4 is an undrilled anomaly in Silurian shales and felsic volcanics where the isotope ratios in B horizon soils are consistent with those of the target isotopic signature.The information from these case histories suggests that the lead isotopic analysis of soils will be a useful exploration tool for concealed mineralization, although at the present stage of research it appears that its application may be limited to shallowly buried (< 100 m) targets or deeply buried targets with an extensive oxidation profile. Its main advantage over conventional geochemical techniques is its ability to discriminate between similar geochemical anomalies arising from different styles of mineralization, as illustrated by an example from Benambra.     

A review of methods used to determine the fractal dimension of linear features

An in-depth review of the more commonly applied methods used in the determination of the fractal dimension of one-dimensional curves is presented. Many often conflicting opinions about the different methods have been collected and are contrasted with each other. In addition, several little known but potentially useful techniques are also reviewed. General recommendations which should be considered whenever applying any method are made.     

Potentiometric and F nuclear magnetic resonance spectroscopic study of fluoride substitution in the GaAl12 polyoxocation: implications for aluminum (hydr)oxide mineral surfaces

Fluoride replacement of oxygens in the GaO₄Al₁₂(OH)₂₄(H₂O)127+(aq) molecule [GaAl₁₂] was studied via ¹⁹F nuclear magnetic resonance (NMR) at 4 < pH < 5 and 278 K in order to elucidate similar reactions at the surfaces of clays. Peaks are identified in the ¹⁹F-NMR spectra that correspond to both terminal and bridging fluorides on the GaAl₁₂ molecule, with relative peak positions similar to those previously identified in fluoridated aluminum (hydr)oxide mineral surfaces (Nordin, J. P., Sullivan, D. J., Phillips, B. L., and Casey, W. H. [1999], “Mechanisms for fluoride-promoted dissolution of bayerite [β-Al(OH)₃(s)] and boehmite [γ-AlOOH(s)]-¹⁹F-NMR spectroscopy and aqueous surface chemistry,” Geochim. Cosmochim. Acta63, 3513-3524). Fluoride substitutes for oxygen at three different sites in the GaAl₁₂ molecule, but at dramatically different rates.The kinetics of fluoride substitution follow a rate law that includes parallel and reversible transfer of fluoride from nonbridging sites to the two bridging sites. The essential features of the rate law are as follows: (1) fluoride replaces bound water molecules (η-OH₂) within minutes at 278 K at rates that are quantitatively similar to fluoride uptake by Al(H₂O)63+(aq) to form AlF²⁺(aq) at similar conditions; (2) fluoride substitutes onto the two topologically distinct μ₂-OH sites at different rates, as was previously observed for oxygen exchange, but here, the reaction is complete in hours to days at 278 K. Most importantly, rates of fluoride substitution onto μ₂-OH sites are 10² times more rapid than the corresponding rates of oxygen exchange with bulk waters, indicating that fluoride considerably labilizes the molecule, as is also observed at the surfaces of minerals. The largest cause of this labilization is the reduced molecular charge on the GaAl₁₂ upon replacement of bound waters by fluoride, which for mineral surfaces corresponds to a reduction in surface charge density.     

Hydrocarbon distribution in coals and in dispersed organic matter of different maceral compositions and maturities

More than 60 samples from 5 coal seams and adjacent siltstones and sandstones were selected from a well through Westphalian B sediments from Northern Germany in order to study bitumen generation and migration. The cores were drilled between 1200 und 1530 metres depth. In this interval, vitrinite reflectance (Rr) is increasing from 0.70 to 0.92%. Results reveal high hydrocarbon generation potentials for all coal samples, but not for adjacent clastic rocks, although maceral compositions of both are quite similar. Yields and compositions of thermal extracts from the coals depend on maceral compositions and rank. However, the bulk of the already generated bitumen has not been removed during natural coalification and is not easily releasable by thermovaporisation. A mass balance based on elemental composition of dull coals indicates that in the rather narrow rank interval (0.70–0.92% Rr) a total mass loss of 20% may have occurred by migration. This is evidenced by a loss of about 20% of the original hydrogen, the rest being stored in the coals.

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Zusammenfassung Um die Entstehung und Migration von Bitumen zu untersuchen wurden in Norddeutschland mehr als 60 Proben aus 5 Kohleflözen und benachbarten Silt- und Sandsteinen aus einer Bohrung durch Westphal B-Sedimente bearbeitet. Die Entnahmetiefe der Bohrkerne liegt zwischen 1200 und 1530 Metern. Innerhalb dieses Intervales steigt die Vitrinit-Reflexion (Rr) von 0,70 auf 0,92%. Für alle Proben aus den Flözen ergeben sich hohe Kohlenwasserstoff-Bildungspotentiale, nicht aber für die benachbarten klastischen Gesteine, obwohl die Mazeral-Zusammensetzungen in beiden ähnlich sind. Die Ausbeute und Zusammensetzung thermaler Extrakte aus den Flözen hängen von Mazeral-Zusammensetzung und Reife ab. Allerdings wurden weder während der Inkohlung größere Mengen des Bitumens abtransportiert, noch ist dieses durch Thermovaporisation leicht freisetzbar. Eine Massenbalanzierung auf der Basis der Elementzusammensetzung ergibt für das relativ schmale Interval von C,70-0,92% Rr ein Massenverlust von 20% durch Migration. Diese Angabe basiert auf einer 20%igen Reduzierung der ursprünglichen Wasserstoffmenge, wobei die restlichen 80% in der Kohle gespeichert bleiben.

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Résumé Dans un forage pratiqué à travers le Westphalien B du nord de l'Allemagne, on a sélectionné plus de 60 échantillons provenant de 5 couches de charbon ainsi que des siltites et grès adjacents, dans le but d'étudier la formation et la migration du bitume. Les carottes proviennent de profondeurs situées entre 1200 et 1530 m. Dans cet intervalle, le pouvoir réflecteur de la vitrinite (Rr) passe de 0,70 à 0,92%. L'étude révèle des potentiels élevés en hydrocarbure pour tous les échantillons de charbon, mais pas pour les roches détritiques voisines, bien que les compositions «macérales» soient analogues dans les deux cas. L'importance et la composition des extrait athermiques des charbons dépendent de la composition «macérale» et du degré d'évolution. Toutefois, la plus grande partie du bitume engendré est restée sur place au cours de la houillification naturelle et elle est difficile à extraire avex la methode de thermovaporisation. Une balance des masses d'éléments indique pour cet intervalle relativement étroit (0,7–0,92% Rr) une perte totale de masse de 20% due à la migration. Ce résultat correspond à une perte d'environ 20% de l'hydrogène originel, les 80% restants étant demeurés dans le charbon.

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Structure and subduction processes along the Oregon-Washington margin

Seismic reflection and refraction data off Washington and Oregon are used to determine the style of sediment deformation and to infer the physical properties of accreted sediments on the lower slope. Onshore-offshore seismic refraction data off Washington are used to determine the location of the trench, or where the plate bending starts.We find that off Washington the subduction zone is characterized by a trench whose physiographic expression is buried under several kilometers of sediments and is tens of kilometers landward of the lower slope, which is accreting seaward as the result of the offscraping of sediments.Seismic reflection data support previous observations that offscraping occurs along seaward and landward dipping thrust faults. Refraction data indicate that a sediment package thrust up along a seaward dipping fault (off Washington) was not measurably changed in velocity with respect to a Cascadia basin section. However a package uplifted by thrusting along a landward dipping fault (off Oregon) did have increased velocity. It is suggested that the increased velocities off Oregon could be the result of erosion and exposure of more deeply buried and compacted sediments, rather than the result of dewatering due to tectonic stress. Off Washington the sensitivity of velocity to porosity and resolution of the seismic method does not preclude dewatering due to tectonic stress, but it does limit the degree of dewatering.In the deeper parts of the lower slope section off Washington and Oregon velocities as high as 3 to 4 km/sec are found. Heat flow data indicate that the temperatures in this high velocity regime are greater than 100°C. It is hypothesized that lithification related to clay diagenesis may be partly responsible for the high velocities, rather than simply compaction. It also appears that the high velocity sediments are subducted while the unlithified low velocity sediments are offscraped.