Time-lapse seismic analysis of pressure depletion in the Southern Gas Basin

In the Southern Gas Basin (SGB) of the North Sea there are many mature gas fields where time‐lapse monitoring could be very beneficial in extending production life. However, the conditions are not immediately attractive for time‐lapse seismic assessment. This is primarily because the main production effect to be assessed is a pore pressure reduction and frame stiffening because of gas production in tight sandstone reservoirs that also have no real seismic direct hydrocarbon indicators. Modelling, based on laboratory measurements, has shown that such an effect would be small and difficult to detect in seismic data. This paper makes two main contributions. Firstly, this is, to our knowledge, the first time‐lapse study in the SGB and involves a real‐data assessment of the viability for detecting production in such an environment. Secondly, the feasibility of using markedly different legacies of data in such a study is addressed, including an assessment of the factors influencing the crossmatching. From the latter, it is found that significant, spatially varying time shifts need to be, and are successfully, resolved through 3‐D warping. After the warping, the primary factors limiting the crossmatching appear to be residual local phase variations, possibly induced by the differing migration strategies, structure, reverberations and different coherencies of the volumes, caused by differences in acquisition‐structure azimuth and acquisition fold. Despite these differences, a time‐lapse amplitude signature is observed that is attributable to production. The character of the 4‐D amplitude anomalies may also indicate variations in stress sensitivity, e.g. because of zones of fracturing. Additionally, warping‐derived time attributes have been highlighted as a potential additional avenue for detection of pressure depletion in such reservoirs. Although the effects are subtle, they may indicate changes in stress/pressure in and around the reservoir because of production. However, to fully resolve the subtle time‐lapse effects in such a reservoir, the data differences need to be better addressed, which may be possible by full re‐processing and pre‐stack analysis, but more likely dedicated 4‐D acquisition would be required.     

Barium- and LREE-rich, olivine-mica-lamprophyres with affinities to lamproites, Mt. Bundey, Northern Territory, Australia

Primitive olivine-mica-K-feldspar lamprophyre dykes, dated at 1831 ± 6 Ma, intrude lower greenschist facies rocks of the Early Proterozoic Pine Creek Inlier, of northern Australia. They are spatially, temporally and probably genetically associated with a post-tectonic composite granite-syenite pluton (Mt. Bundey pluton). The dykes have unusually high contents of large-ion-lithophile (LILE) and LREE elements (e.g. Ba up to 10,000 ppm, Ce up to 550 ppm, K₂O up to 7.5 wt. %) that resemble the concentrations found in the West Kimberley olivine and leucite lamproites. However, mineralogically the Mt. Bundey lamprophyres resemble shoshonitic lamprophyres and lack any minerals diagnostic of lamproites; leucite or leucite-pseudomorphs are absent. Mineral compositions are also unlike those in lamproites: micas contain higher Al₂O₃ than lamproitic mica; amphiboles are secondary actinolites after diopside; and oxides consist of zincian-chromian magnetite and groundmass magnetite. Heavy mineral concentrates contain mantle-derived xenocrysts of magnesiochromite, pyrope, Cr-diopside and rutile indicating a depth of sampling > 70 km. The Mt. Bundey lamprophyres are non-peralkaline to borderline peralkaline (molar (K + Na)/Al = 0.8 − 1.0) and potassic rather than ultrapotassic (molar K/Na < 2.5). They have distinctive major element compositions (≈46−49 wt. % SiO₂, ≈1.5−2 wt. % MgO, ≈7 wt. % CaO), and element ratios (e.g. molar Al/Ti ≈10, K/Na ≈2) that indicate they are best classified amongst transitional lamproites, i.e. potassic rocks such as cocites, jumillites and Navajominettes, that have geochemical characteristics transitional between Groups I and III. (Foley et al., 1987). The Mt. Bundey lamprophyres have LILE enrichment patterns that resemble the W. Kimberley pamproites but have moderate negative Ta---Nb---Ti anomalies and HREE abundances that are closely similar to the jumillites of southeastern Spain and Mediterranean-type lamproites. Single-stage modelling of Rb---Sr data is consistent with enrichment of the source-region of the Mt. Bundey lamprophyres ≈ 120–170 Ma before partial melting; i.e. at 1.95–2.10 Ga. Source enrichment does not appear to be associated with subduction processes, but may instead relate to incipient rifting of the Archaean basement. Negative Ta---Nb---Ti anomalies in the Mt. Bundey dykes may, therefore, relate to stability of residual titanate minerals in an oxidized subcontinental mantle source. This view is supported by high Fe³⁺/ΣFe ratios of mantle-derived magnesiochromite xenocrysts which indicate oxidized mantle conditions (ƒ_o2 ≈ FMQ + 1 long units), and by the presence of xenocrystic Cr-bearing rutile. Although the Mt. Bundey dykes have sampled upper mantle material, the oxidized nature of the magma source-region, and of the magma itself, suggests that conditions may not be favourable for diamond survival at depth nor for diamond transport in transitional lamproite magmas of this kind.     

The effect of As, Co, and Ni impurities on pyrite oxidation kinetics: Batch and flow-through reactor experiments with synthetic pyrite

Pyrite samples synthesized with As, Co, or Ni impurities and without added impurities were oxidized in batch and mixed flow-through reactors in the presence of 1 mM ferric iron, at pH 2. Six samples from each dopant population were used to provide a statistically robust comparison; two natural samples from Leadville, CO (major impurities Pb, As, Bi, Ag, Zn) and Elba, Italy (Co, As) were also included. In each experiment, three reaction progress variables were monitored: ferric iron, ferrous iron, and sulfate. The pyrite samples with impurities have average oxidation rates that are faster than the undoped samples, with As- and Co-doped pyrite having the highest rates. As, Co, and Ni were released to solution in accordance with their concentrations in the solid samples. As concentrations in the batch reactor experiments tended to remain constant, in contrast to Co and Ni, which increased over time. Initial rates, calculated from the batch reactor experiments, were faster than the steady-state rates calculated from the mixed flow-through reactor experiments. Apparent rates calculated using sulfate were faster than apparent rates calculated using ferric and ferrous iron, reflecting oxidation of ferrous iron in solution by dissolved oxygen. The results imply that impurities in pyrite do contribute to its reactivity, in agreement with studies using electrochemical methods. Oxidation rate differences among pyrite samples with different impurities are probably too small to warrant explicit consideration in environmental modeling applications, but are important to understanding pyrite oxidation mechanisms and semiconducting properties.     

Grain size along two gravel-bed rivers: statistical variation,spatial pattern and sedimentary links

A new set of field data facilitates a detailed analysis of variations in bed material grain size within two confluent gravel-bed rivers in northeastern British Columbia, Canada. A preliminary assessment of grain-size variability establishes a basis for examination of the spatial pattern of grain-size change. Standard ANOVA techniques are inappropriate because individual samples have unequal variances and are not normally distributed. Alternative tests for homoscedasticity and comparison of means are therefore utilized. Within-site, between-sample variability is not significant. The grain-size distributions that were obtained at individual sites are therefore representative of the depositional environments that were sampled. In both rivers mean grain size does vary significantly between sites and there is therefore a basis for examining the data for spatial patterns such as downstream fining. Textural variations along the two rivers studied here are complex and show negligible overall fining (in over 100 km). This is the consequence of a large number of tributary inputs and non-alluvial sediment sources which are the legacy of Late Pleistocene glaciation. The identification of lateral sources like these is fundamental for understanding textural changes within rivers. The sedimentary link (a channel reach between significant lateral sediment inputs) provides a means of isolating fluvial maturation processes (abrasion and sorting) from contingent lateral inputs. Strong fining trends are apparent in most links and classification of grain-size measurements according to their location within particular links greatly improves the statistical explanation of textural variation. Identification of sedimentary links provides a means of applying models of fluvial fining processes, so isolation of link networks will aid the development of basin-scale models of textural variation. © 1998 John Wiley & Sons, Ltd.     

State of stress in the lithosphere: Inferences from the flow laws of olivine

The experimental flow data for rocks and minerals are reviewed and found to fit a law of the form $$\dot \varepsilon = A'\left[ {sinh (\alpha \sigma )} \right]^n \exp \left[ {{{ - (E * + PV * )} \mathord{\left/ {\vphantom {{ - (E * + PV * )} {RT}}} \right. \kern-\nulldelimiterspace} {RT}}} \right]$$ where \(\dot \varepsilon \) This law reduces to the familiar power-law stress dependency at low stress and to an exponential stress dependency at high stress. Using the material flow law parameters for olivine, stress profiles with depth and strain rate are computed for a representative range of temperature distributions in the lithosphere. The results show that the upper 15 to 25 km of the oceanic lithosphere must behave elastically or fail by fracture and that the remainder deforms by exponential law flow at intermediate depths and by power-law flow in the rest. A model computation of the gravitational sliding of a lithospheric plate using olivine rheology exhibits a very sharp decoupling zone which is a consequence of the combined effects of increasing stress and temperature on the flow law, which is a very sensitive function of both.     

The nature of crystalline silica from the TAG submarine hydrothermal mound, 26°N Mid Atlantic Ridge

Silica occurs in abundance in a variety of hydrothermal samples from the Trans-Atlantic Geotraverse (TAG) hydrothermal mound, 26°N Mid-Atlantic Ridge. The water content, trace element chemistry, and mineralogy of crystalline silica from 15 different samples have been examined by vibrational spectroscopy and probe microanalysis. The samples are from: shallow subsurface ferric iron oxyhydroxide silica deposits (n=4), a fragment of an active white smoker chimney (n=1), anhydrite bearing hydrothermal breccias (n=2), pyrite silica breccias (n=3), and silicified wall rock breccias (n=5). Length-fast chalcedony occurs in association with variable quantities of ferric iron oxyhydroxides in hydrothermal breccias from the mound flanks, within shallower subsurface chert samples, and within white smoker chimney walls. Samples from the anhydrite zone contain textures which are suggestive of an origin involving replacement of anhydrite. Samples taken from TAG 1 and 5 from below the anhydrite zone contain no chalcedony. Instead they contain subhedral quartz crystals which show oscillatory zoning in aluminium. Two types of crystalline silica namely, type A and type B quartz, are defined on the basis of the infrared spectra in the OH region from 3200 cm⁻¹ to 3600 cm⁻¹. The type A quartz occurs beneath the anhydrite zone at TAG 1 and 5. We propose a model that relates specific varieties of crystalline silica to different thermal and chemical environments within the mound interior. Length-fast chalcedony occurs in an outer low temperature envelope across the top and sides of the mound. The common association between length-fast chalcedony and ferric iron oxyhydroxides suggests that chalcedony crystallization is favoured where catalysis by ferric iron can occur. The apparent suppression of fibrous silica at the expense of single quartz crystals with increasing depth is attributed to differing growth rates and degrees of supersaturation of silica-bearing solutions with increasing temperature within the mound. The transition from type A to type B single crystal growth is interpreted to occur at temperatures approaching ˜360 °C due to decreasing solubility of aluminium in quartz, so that aluminium is rendered unavailable for type A valence compensation. Received: 10 September 1998 / Accepted: 6 July 1999