Isotopic evidence of TSR origin for natural gas bearing high H<Subscript>2</Subscript>S contents within the Feixianguan Formation of the northeastern Sichuan Basin,southwestern China

The northeastern area of Sichuan Basin, southwestern China, is the area with the maximal reserve of natural gas containing higher hydrogen sulphide (H₂S) that has been found among the petroliferous basins of China, with the proven and controlled gas reserve of more than 200 billion cubic meters. These gas pools, with higher H₂S contents averaging 9%, some 17%, are mainly distributed on structural belts of Dukouhe, Tieshanpo, Luojiazhai, Puguang, etc., while the oolitic-shoal dolomite of the Triassic Feixianguan Fm. (T₁f) is the reservoir. Although many scholars regard the plentiful accumulation of H₂S within the deep carbonate reservoir as the result of Thermochemical Sulfate Reduction (TSR), however, the process of TSR as well as its residual geological and geochemical evidence is still not quite clear. Based on the carbon isotopic analysis of carbonate strata and secondary calcite, etc., together with the analysis of sulfur isotopes within H₂S, sulphur, gypsum, iron pyrites, etc., as well as other aspects including the natural gas composition, carbon isotopes of hydrocarbons reservoir petrology, etc., it has been proved that the above natural gas is a product of TSR. The H₂S, sulphur and calcite result from the participation of TSR reactions by hydrocarbon gas. During the process for hydrocarbons being consumed due to TSR, the carbons within the hydrocarbon gas participate in the reactions and finally are transferred into the secondary calcite, and become the carbon source of secondary calcite, consequently causing the carbon isotopes of the secondary calcite to be lower (−18.2‰). As for both the intermediate product of TSR, i.e. sulfur, and its final products, i.e. H₂S and iron pyrites, their sulfur elements are all sourced from the sulfate within the Feixianguan Fm. During the fractional processes of sulfur isotopes, the bond energy leads to the ³²S being released firstly, and the earlier it is released, the lower δ ³⁴S values for the generated sulphide (H₂S) or sulfur will be. However, for the anhydrite that participates in reactions, the higher the reaction degree, the more ³²S is released, while the less ³²S remains and the more δ ³⁴S is increased. The testing results have proved the process of the dynamic fractionation of sulfur isotopes.     

<Superscript>40</Superscript>Ar/<Superscript>39</Superscript>Ar chronology and geochemistry of high-K volcanic rocks in the Mangkang basin,Tibet

Our two newly obtained high-quality ⁴⁰Ar/³⁹Ar ages suggest that the high-K volcanic rocks of the Lawuxiang Formation in the Mangkang basin, Tibet were formed at 33.5 ± 0.2 Ma. The tracing of elemental and Pb-Sr-Nd isotopic geochemistry indicates that they were derived from an EM2 enriched mantle in continental subduction caused by transpression. Their evidently negative anomalies in HFSEs such as Nb and Ta make clear that there is an input of continental material into the mantle source. The high-K rocks at 33.5 ± 0.2 Ma in the Mangkang basin may temporally, spatially and compositionally compare with the early one of two-pulse high-K rocks in eastern Tibet distinguished by Wang J. H. et al., implying that they were formed in the same tectonic setting.     

Sudden enhancement of sedimentation flux of <Superscript>210</Superscript>Pb<Subscript>ex</Subscript> as an indicator of lake productivity as exemplified by Lake Chenghai

The fundamental assumption of ²¹⁰Pb sediment dating is the stable flux of ²¹⁰Pb_ex, which was derived from atmosphere and then transferred into sediments via lake water. When the sedimentation rate is relatively constant, the ²¹⁰Pb_ex activity in sediments will be exponentially reduced with sedimentation age. ²¹⁰Pb_ex in lake water is incorporated into sediments mainly via organic particulates. If the sedimentation flux of organic matter in lake water is suddenly increased, ²¹⁰Pb_ex will be significantly deposited and then transferred into sediments. On the one hand such sudden purification effect is obviously unfit for the fundamental assumption of ²¹⁰Pb dating; on the other hand, the sudden enhancement of ²¹⁰Pb_ex flux would be indicative of the conspicuous variation of primary productivity of lake water. This problem will be discussed in accordance with the variation trend of ²¹⁰Pb_ex in the vertical profile of recent sediments of Lake Chenghai, Yunnan Province. The sediment core was collected from the deep-water area of Lake Chenghai in June 1997. The vertical profile of ¹³⁷Cs activity is characterized by a tree-peak pattern. This profile gave reliable ages, and also showed the stability of sediment accumulation in the recent ten years. The vertical profile of ²¹⁰Pb_ex activity displays a specific distribution of peaks, and is similar to the vertical profile of C_org. This phenomenon seems to be related to the mechanism of constraining the transfer of ²¹⁰Pb_ex into lake sediments. The average atomic ratios of H_org/C_org and C_org/N_org in Lake Chenghai sediments are 5.51 and 7.04, respectively, indicating that the organic matter was predominantly derived from the remains of endogenic algae. In terms of the three-stage evolutionary characteristics of organic matter in sediments, i.e., “deposition-de-composition-accumulation”, the sedimentation fluxes (F(C_org)) of organic carbon (C_org) since 1970 were calculated by modeling. The sedimentation fluxes of ²¹⁰Pb_ex (F(²¹⁰Pb_ex)) in different years display good synchronous relations with the sedimentation flux of organic carbon (F(C_org)), especially in the years of 1972–1974 and 1986–1989. The variation of F(C_org) led to the variation of F(²¹⁰Pb_ex); the variation of F(²¹⁰Pb_ex) reflects, to some extent, the historical variation of lake productivity.     

The crystal structure of (Fe<Subscript>4</Subscript>Cr<Subscript>4</Subscript>Ni)<Subscript>9</Subscript>C<Subscript>4</Subscript>

(Fe4Cr4Ni)9C4 is a metal carbide mineral formed by combination of Fe, Cr and Ni with C. It occurs in a chromite deposit in the Luobusha ophiolite, Tibet. Based on the determination of its crystal structure, the empirical formula is (Fe4.12Cr3.84Ni0.96)8.92C3.70 and the simplified formula is (Fe4Cr4Ni)4C9. The mineral is hexagonal with a = 1.38392(2) nm, c = 0.44690(9) nm, pace group P63 m c, Z=6 and the calculated specific gravity Dx = 7.089 g/cm3. Fe, Cr and Ni occupy different crystallographic sites and their coordination numbers are approximately 12, forming an alternate stacking sequence of flat and puckered layers along the c axis. Some metallic atoms have a defect structure. The interatomic distances of Fe, Cr and Ni are 0.2525-0.2666 nm, and the distances between Fe, Cr, Ni and C are 0.1893-0.2169 nm. The coordination number of carbon is 6. It occurs in interstices of the metallic atoms Fe, Cr and Ni to form trigonalprismatically coordinated polyhedra. These coordination polyhedra are linked with each other via shared corners or shared edges into a new type of metal carbide structure.     

Treatment of ground-motion predictive relationships for the reference seismic hazard map of Italy

In the framework of the 2004 reference seismic hazard map of Italy the amplitude of the strong-motion (expressed in terms of Peak Horizontal Acceleration with 10% probability of non-exceedence in 50 years, referred to average hard ground conditions) was computed using different predictive relationships. Equations derived in Italy and in Europe from strong-motion data, as well as a set of weak and strong-motion based empirical predictive relationships were employed in a logic tree procedure, in order to capture the epistemic uncertainty affecting ground-motion attenuation. This article describes the adjustments and conversions required to eliminate the incompatibilities amongst the relations. Particularly significant are distance conversions and style-of-faulting adjustments, as well as the problems related to the use of regional relations, such as the selection of a reference depth, the quantification of random variability and the strong-motion prediction. Moreover, a regional attenuation relationship specific for volcanic areas was also employed, allowing a more realistic evaluation of seismic hazard, as confirmed by the attenuation of macroseismic intensities.     

Characteristics of the low energy seismicity of central Apulia (southern Italy) and hazard implications

The central part of the Apulia region, in southern Italy, has been generally considered practically free from significant level of seismicity, but historical documentation, geological indicators and recent instrumental observations suggest that the activity of local minor tectonic structures could have been masked (and partly also induced) by that of major seismogenic structures located in the neighbouring regions. A revision of the central Apulia seismicity characteristics was conducted considering its space and time distribution, energy release rate and focal mechanisms, in view of possible hazard implications. To better constrain the seismicity rates inferable from the set of available historical data, special attention was paid to the declustering of a catalogue of low energy events (magnitude < 3.5) instrumentally detected in about 20 years: a new declustering procedure, useful for cases like to the one at hand, was purposely devised taking into account the peculiarity of local seismicity characteristics and the limitations of the available database. The results obtained by combining instrumental and historical data show that this area is affected by a rather sporadic seismicity, likely associated to a general tensional regime and possibly stimulated by the interaction with Apenninic and northern Apulia seismogenic activity. Even though less energetic, the local seismicity contributes to increase the moderately damaging shaking probability due to the activity of seismic sources located in the near areas, so to justify the adoption of at least a minimum level of caution in relation to the local definition of seismic protection measures.     

NMR Measurements in Carbonate Rocks: Problems and an Approach to a Solution

Carbonate rocks are well known for their complex petrophysical behavior where, in contrast to siliciclastic rocks, different parameters, including porosity and permeability, usually are not directly related. This behavior is the result of thorough reorganization of porosity during diagenesis, and it turns prediction of reservoir quality of carbonate rocks into a challenge. The study presented here deals with the problem of utilizing NMR techniques in prediction of petrophysical properties in carbonates.We employ a visual porosity classification as a priori knowledge for better interpreting NMR data for prediction purposes. This allows for choice of suitable T₂ cutoff values to differentiate movable from bound fluids adapted for the specific carbonate rock, thus resulting in better interpretation of NMR data. The approach of using a genetic pore type classification for adapting the conventional method for T₂ cutoff determination, which originally was developed for siliciclastic rocks, is promising. Similarly, for permeability determination on the basis of NMR measurements, the classification of carbonate rocks based on porosity types also shows potential. The approach implemented here has the promise to provide a basis of standardized interpretation of NMR data from carbonate rocks.Acknowledgment We are grateful to Baker Hughes INTEQ, Celle, for permission to publish the results of this work. This study was part of I.S.s Masters Thesis at Hannover University that was carried out in collaboration with Baker Hughes INTEQ, Celle, Germany. We appreciate comments of an anonymous referee and PAGEOPH editor Brian J. Mitchell.     

Three-Dimensional Electromagnetic Modelling and Inversion from Theory to Application

The whole subject of three-dimensional (3-D) electromagnetic (EM) modelling and inversion has experienced a tremendous progress in the last decade. Accordingly there is an increased need for reviewing the recent, and not so recent, achievements in the field. In the first part of this review paper I consider the finite-difference, finite-element and integral equation approaches that are presently applied for the rigorous numerical solution of fully 3-D EM forward problems. I mention the merits and drawbacks of these approaches, and focus on the most essential aspects of numerical implementations, such as preconditioning and solving the resulting systems of linear equations. I refer to some of the most advanced, state-of-the-art, solvers that are today available for such important geophysical applications as induction logging, airborne and controlled-source EM, magnetotellurics, and global induction studies. Then, in the second part of the paper, I review some of the methods that are commonly used to solve 3-D EM inverse problems and analyse current implementations of the methods available. In particular, I also address the important aspects of nonlinear Newton-type optimisation techniques and computation of gradients and sensitivities associated with these problems.