Three‐dimensional nonlinear finite element analysis of pile groups in saturated porous media using a new transmitting boundary

The dynamic behaviour of pile groups subjected to an earthquake base shaking is analysed. An analysis is formulated in the time domain and the effects of material nonlinearity of soil, pile–soil–pile kinematic interaction and the superstructure–foundation inertial interaction on seismic response are investigated. Prediction of response of pile group–soil system during a large earthquake requires consideration of various aspects such as the nonlinear and elasto‐plastic behaviour of soil, pore water pressure generation in soil, radiation of energy away from the pile, etc. A fully explicit dynamic finite element scheme is developed for saturated porous media, based on the extension of the original formulation by Biot having solid displacement (u) and relative fluid displacement (w) as primary variables (u–w formulation). All linear relative fluid acceleration terms are included in this formulation. A new three‐dimensional transmitting boundary that was developed in cartesian co‐ordinate system for dynamic response analysis of fluid‐saturated porous media is implemented to avoid wave reflections towards the structure. In contrast to traditional methods, this boundary is able to absorb surface waves as well as body waves. The pile–soil interaction problem is analysed and it is shown that the results from the fully coupled procedure, using the advanced transmitting boundary, compare reasonably well with centrifuge data. Copyright © 2007 John Wiley & Sons, Ltd.     

Limiting equilibrium method for slope/drilled shaft system

The use of drilled shafts to stabilize an unstable slope has been a widely accepted practice. There are two basic design and analysis issues involved: one is to determine the global factor of safety of the drilled shafts stabilized slope and the other one is to determine the design earth thrust on the drilled shafts for structural design of the shafts. In this paper, a limiting equilibrium method of slices based solution for calculating global factor of safety (FS) of a slope with the presence of a row of drilled shafts is developed. The arching mechanisms due to the presence of the drilled shafts on slope were taken into account by a load transfer factor. The method for calculating the net force applied to the drilled shaft from the soil mass was also developed. The interrelationships among the drilled shaft location on the slope, the load transfer factor, and the global FS of the slope/shaft system were derived utilizing the developed numerical closed‐form solution. An illustrative example is presented to elucidate the use of the solution in optimizing the location of the drilled shafts on slope to achieve the desired global factor of safety of the slope/shaft system. Copyright © 2009 John Wiley & Sons, Ltd.     

Mineral chemical composition and geodynamic significance of peridotites from Nain ophiolite,central Iran

The peridotites from north of the town of Nain in central Iran consist of clinopyroxene-bearing harzburgite and lherzolite with small lenses of dunite and chromitite pods. The lherzolite contains aluminous spinel with a Cr number (Cr^# = Cr/[Cr + Al]) of 0.17. The Cr number of spinels in harzburgite and chromitite is 0.38–0.42 and 0.62, respectively. This shows that the lherzolite and harzburgite resulted from <18% of partial melting of the source materials. The estimated temperature is 1100 ± 200 °C for peridotites, the estimated pressure is <15 ± 2.3 kbar for harzburgites and >16 ± 2.3 kbar for lherzolites and estimated fo₂ is 10^?1±0.5 for peridotites. Discriminant geochemical diagrams based on mineral chemistry of harzburgites indicate a supra-subduction zone (SSZ) to mid-oceanic ridge (MOR) setting for these rocks. On the basis of their Cr^#, the harzburgite and lherzolite spinels are analogous to those from abyssal peridotites and oceanic ophiolites, whereas the chromites in the chromitite (on the basis of Cr^# and boninitic nature of parental melts) resemble those from SSZ ophiolitic sequences. Therefore, the Nain ophiolite complex most likely originated in an oceanic crust related to supra-subduction zone, i.e. back arc basin. Field observations and mineral chemistry of the Nain peridotites, indicating the suture between the central Iran micro-continent (CIM) block and the Sanandaj–Sirjan zone, show that these peridotites mark the site of the Nain–Baft seaway, which opened with a slow rate of ocean-floor spreading behind the Mesozoic arc of the Sanandaj–Sirjan zone as a result of change of Neo Tethyan subduction régime during middle Cretaceous.     

Development in modeling cyclic loading of sands based on kinematic hardening

In this paper, there is presented an elastoplastic constitutive model to predict sandy soils behavior under monotonic and cyclic loadings. This model is based on an existing model (Cambou‐Jafari‐Sidoroff) that takes into account deviatoric and isotropic mechanisms of plasticity. The flow rule used in the deviatoric mechanism is non‐associated and a mixed hardening law controls the evolution of the yield surface. In this research the critical state surface and history surface, which separates the virgin and cyclic states in stress space, are defined. Kinematic hardening modulus and stress–dilatancy law for monotonic and cyclic loadings are effectively modified. With taking hardening modulus as a function of deviatoric and volumetric plastic strain and with defining the history surface and stress reversal, the model has the ability to predict the sandy soils' behavior. All of the model parameters have clear physical meanings and can be determined from usual laboratory tests. In order to validate the model, the results of homogeneous tests on Hostun and Toyoura sands are used. The results of validation show a good capability of the proposed model. Copyright © 2009 John Wiley & Sons, Ltd.     

List of forthcoming papers

List of forthcoming papers     

Intellectual property rights and the transfer of climate change technologies: issues,challenges, and way forward

The role of intellectual property rights (IPRs) in the development and transfer of climate change technologies has been a contentious issue in negotiations under the United Nations Framework Convention on Climate Change (UNFCCC). Irreconcilable differences seem to oppose those who believe IPRs are an inherent barrier to the transfer of climate change technologies and those who argue they are an essential incentive to innovation. After providing an overview of the polarized debate on this issue, this article reviews the existing literature and empirical evidence and looks into some practical initiatives and recent developments. Finally, it seeks to identify a way forward that could help overcome the current stalemate in international deliberations by suggesting a number of parameters to structure the discussion on this complex issue.     

High oxidation state during formation of Martian nakhlites

Abstract– The oxygen fugacities recorded in the nakhlites Nakhla, Yamato‐000593 (Y‐000593), Lafayette, and NWA998 were studied by applying the Fe,Ti‐oxide oxybarometer. Oxygen fugacities obtained cluster closely around the FMQ (Fayalite–Magnetite–Quartz) buffer (NWA998 = FMQ ? 0.8; Y‐000593 = FMQ ? 0.7; Nakhla = FMQ; Lafayette = FMQ + 0.1). The corresponding equilibration temperatures are 810 °C for Nakhla and Y‐000593, 780 °C for Lafayette and 710 °C for NWA998. All nakhlites record oxygen fugacities significantly higher and with a tighter range than those determined for Martian basalts, i.e., shergottites whose oxygen fugacities vary from FMQ ? 1 to FMQ ? 4. It has been known for some time that nakhlites are different from other Martian meteorites in chemistry, mineralogy, and crystallization age. The present study adds oxygen fugacity to this list of differences. The comparatively large variation in fO₂ recorded by shergottites was interpreted by Herd et al. (2002) as reflecting variable degrees of contamination with crustal fluids that would also carry a light rare earth element (REE)‐enriched component. The high oxygen fugacities and the large light REE enrichment of nakhlites fit qualitatively in this model. In detail, however, it is found that the inferred contaminating phase in nakhlites must have been different from those in shergottites. This is supported by unique ¹⁸²W/¹⁸⁴W and ¹⁴²Nd/¹⁴⁴Nd ratios in nakhlites, which are distinct from other Martian meteorites. It is likely that the differences in fO₂ between nakhlites and other Martian meteorites were established very early in the history of Mars. Parental trace element rich and trace element poor regions (reservoirs) of Mars mantle ( Brandon et al. 2000 ) must have been kept isolated throughout Martian history. Our results further show significant differences in closure temperature among the different nakhlites. The observed range in equilibration temperatures together with similar fO₂ values is attributable to crystallization of nakhlites in the same cumulate pile or lava layer at different burial depths from 0.5 to 30 m below the Martian surface in agreement with Mikouchi et al. (2003) and is further confirmed by similar crystallization ages of about 1.3 Ga ago (e.g., Misawa et al. 2003 ).     

Petrology and geochemistry of greywackes from Goa-Dharwar sector,western Dharwar Craton: Implications for volcanoclastic origin

Late Archaean Supracrustals of the Goa-Dharwar sector (GDS) are composed of a thick sequence of greywacke sequence with narrow intercalations of quartzite, BIF and carbonates. Mafic volcanics occupy the base of the sequence. The greywackes are predominantly tuffacious containing chlorite-sericite and hornblende. Arkosic variations containing biotite dominate the western part of the sector. Fine-grained variations occur as isolated narrow lenses within other types of greywackes. The conglomeratic greywackes are localized along the western and the eastern margins of the sector. All of the greywackes are all typically immature containing coarser clasts of mostly plagioclase (18–23%) and quartz (32–34%). Lithic fragments of felsic volcanic rocks are common. The matrix is dominated by mafic material. Biotite and amphibole are related to metamorphic recrystallization. Chlorite, sericite, epidote, carbonate and chert are products of the interplay of diagenesis and low-grade metamorphism. Fe-Ti oxide, sphene, apatite and zircon are usual accessories. But for slight enrichment in K₂O, the major element chemistry of the GDS greywackes is similar to the chemistry of Late Archaean greywackes. They also compare in respect of V, Co, Hf contents, K₂O/Na₂O, SiO₂/Al₂O₃, Na₂O/Al₂O₃, Ba/Rb, Th/U, La/Th, Sm/Nd ratios, steep REE patterns with distinct LREE enrichment and HREE depletion. The GDS greywackes however are distinctly enriched in Rb, Ba, Sr, Th, U, Cu, Zr, Ce/Ce* and depleted in Cr, Ni, and Zn. The conglomeritic and biotite bearing verities contain considerable proportions of clasts derived from the basement tonalitic/granitic terrain. The common tuffacious greywackes containing hornblende and biotite-sericite however include only volcanic clasts and bear evidence of derivation from submarine weathering of predominantly felsic volcanics erupted on a large scale to form a magmatic arc in the later stages of geosynclinal deposition. Geochemical data suggest that the GDS greywackes were laid down in progressively changing basin geometry from a passive to active continental margin and island arc setting.     

Evolution of isotopic compositions in groundwater of the area between the Gulf of Oman and the Arabian Gulf

The stable isotopes of oxygen and hydrogen have been implemented to assess the recharge mechanisms in an area in the UAE bounded to the northwestern part of the Gulf of Oman and the southeastern part of the Arabian Gulf. The conversion of stable isotopes to deuterium excess was utilized as a supportive tool to understand the process of groundwater recharge. The concluding results of this study showed that the origin of moisture is the Mediterranean Sea. The precipitation is the main source of recharge, in which the precipitation having undergone evaporation before recharge occurs. The comparison between regression line for data collected in 1996 and regression line for samples collected in 2006 suggests that the precipitation water which recharged the groundwater, was diluted with groundwater and this dilution is observed from decreasing of the deuterium excess of collected groundwater samples with increasing isotopes of oxygen. The dilution of groundwater with the recharge water suggests modern-day recharge as it is seen from high deuterium excess that exceeded the deuterium excess of LMWL and was close to MMWL.