Quality assessment and hydrogeochemical characteristics of groundwater in Agastheeswaram taluk,Kanyakumari district,Tamil Nadu,India

The present study investigates the hydrogeochemical characteristics of groundwater quality in Agas- theeswaram taluk of Kanyakumari district, Tamil Nadu, India. A total of 69 groundwater samples were collected during pre- and post-monsoon periods of 2011-2012. The groundwater quality assessment has been carried out by evaluating the physicochemical parameters such as pH, EC, TDS, HCO3, Cl, SO42-, Ca2＋, Mg2＋, Na＋ and K＋ for both the seasons. Based on these parameters, groundwater has been assessed in favor of its suitability for drinking and irrigation purpose. Dominant cations for both the seasons are in the order of Na＋〉 Ca2＋〉 Mg2＋ 〉 K＋ while the dominant anions for post monsoon and pre monsoon have the trends of CI 〉 HCO3 〉 SO42- and HCO3- 〉 CI 〉 SO42-, respectively. Analytical results observed from various indices reveal that the groundwater quality is fairly good in some places. Analytical results of few samples show that they are severely polluted and incidentally found to be near the coasts, estuaries and salt pans in the study area. The Gibbs plot indicates that the majority of groundwater samples fall in rock dominant region, which indicates rock water interaction in the study area. The United States salinity （USSL） diagram shows that the groundwater is free from sodium hazards but the salinity hazard varies from low to very high throughout the study area. This reveals that the groundwater is moderately suitable for agricultural activities. The observed chemical variations in pre-monsoon and post-monsoon seasons may be the effect to rock-water interactions, ion-exchange reactions, and runoff of fertilizers from the surrounding agricultural lands.     

Investigation of surface and subsurface displacements due to multiple tunnels excavation in urban area

Underground structures are currently widely used and are built as urbanism develops. The interactions between perpendicularly crossing and parallel tunnels in the Tehran region are investigated by using a full three-dimensional (3D) finite difference analysis with elastic-plastic material models. Special attention is paid to the effect of subsequent tunneling on the support system, i.e., the shotcrete lining and rock bolts of the existing tunnel. Eventually, as the tunnels are excavated at certain levels, the interaction between the tunnels will certainly have a significant influence on both stress distribution and consequently deformations. Since multilayer tunneling is a three-dimensional phenomenon in nature, 3D numerical solutions must be utilized for analyzing effect of perpendicularly crossing tunnels at various levels. As Tohid twin tunnels and Line 7 pass beneath the Line 4 metro tunnel, changes in stress distribution, deformations, and surface settlements are studied for various conditions and the results are presented in this paper. Consequently, it is shown that there is a significant interaction between tunnels that necessitate certain preventive measures to maintain a stable tunneling operation.     

Mapping of seawater inundation along Nagapattinam based on field observations

Nagapattinam, in the east coast of India, was severely affected during the deadliest Indian Ocean tsunami of December 26, 2004. The tsunami caused heavy damage to life and property, and the death toll was about 3,378 in Nagapattinam taluk. Certain villages along the coast witnessed large inundation while adjacent villages were protected from the fury of the tsunami waves. This study was carried out to examine the underlying causes for the vulnerability along Nagapattinam coast with the help of field observations, remote sensing, and geographical information system as tools. Coastal areas with high sand dunes have been protected from tsunami, and areas adjacent to backwaters were inundated. Realtime Kinematic Global Positioning System and high-resolution satellite data were used to map the topographic information and maximum extent of inundation. Thematic maps on land use, land cover, and coastal geomorphology were generated using remote sensing and field data. Using field data as the primary source of information, tsunami hazard maps have been generated for Nagapattinam.     

Mafic dykes derived from Early Cretaceous depleted mantle beneath the Dabie orogenic belt: implications for changing lithosphere mantle beneath Eastern China

SHRIMP zircon U–Pb geochronological, elemental and Sr–Nd isotopic data from Early Cretaceous mafic dykes in North Dabie orogenic belt elucidate a change of Mesozoic lithospheric mantle in eastern China. The dykes are predominantly dolerite with the major mineral assemblage clinopyroxene + hornblende + plagioclase and yield a SHRIMP zircon U–Pb age of 111.6 ± 5.3 Ma. They have a narrow range of SiO₂ from 46.16% to 49.78%, and relative low concentrations of K₂O (1.07−2.62%), Na₂O (2.45−3.54%), Al₂O₃ (13.04−14.07%), and P₂O₅ (0.42−0.55%) but relatively high concentration of MgO (5.94–6.61%) with Mg^# 52–54. All the samples are characterized by enrichment of large ion lithophile elements (LILE, e.g., Ba, Th) and high field strength elements (HFSE, e.g., Nb, Ti). (⁸⁷Sr/⁸⁶Sr)_i ratios from 0.704 to 0.705, ε_Nd values from 3.36 to 4.33 and mantle‐depletion Nd model ages (T_2DM) in the range 0.56–0.64 Ga indicate that the magma of the Baiyashan mafic dykes was derived from a young depleted mantle source. This finding is different from previous research on mafic dykes in the age range 120–138 Ma that revealed enrichment of LILE and depletion of HFSE, high initial Sr isotopic ratios and negative ε_Nd, value which represents an old enriched mantle source. Ours is the first report of the existence of Early Cretaceous depleted mantle in eastern China and it implies that changing of enriched mantle to depleted mantle occurred at ca. 112 Ma, associated with back‐arc extension which resulted from the subduction of the Palaeo‐Pacific Plate towards the Asian Continent. Copyright © 2010 John Wiley & Sons, Ltd.     

Hydrogen peroxide interference in chemical oxygen demand during ozone based advanced oxidation of anaerobically digested livestock wastewater

It is known that hydrogen peroxide interferes with chemical oxygen demand analysis by consuming oxidation agents such as potassium dichromate, thus leading to overestimation of the chemical oxygen demand measurements. The objective of the study was to investigate the effects of hydrogen peroxide interference and to determine true chemical oxygen demand values on interpreting treatment performance during ozone-based advanced oxidation of livestock wastewater in which hydrogen peroxide concentration and chemical oxygen demand values are dynamically changing. According to the chemical oxygen demand monitoring data, chemical oxygen demand values were always higher than the initial chemical oxygen demand load when hydrogen peroxide was involved and the treatment performance with ozone alone or ozone/ultraviolet was better than with coupled hydrogen peroxide. The extent of overestimation was proportional to the remaining hydrogen peroxide concentration and the average overestimation ratio in livestock wastewater was in the range of 0.50～0.58 mg per 1 mg of hydrogen peroxide, depending upon the quality of the wastewater treated. True chemical oxygen demand values were estimated by correlating the extent of overestimation with the remaining hydrogen peroxide concentration during treatment. The extent of overestimation decreased to zero gradually as the amount of hydrogen peroxide also approached zero as oxidation proceeded. The corrected chemical oxygen demand values indicated underlying tendency of oxidation, which could not be seen in the original chemical oxygen demand monitoring data. Application of ozone/hydrogen peroxide was more efficient for reducing chemical oxygen demand than ozone alone, as was ozone/hydrogen peroxide/ultraviolet compared to ozone/ultraviolet. When coupled with ozone, ultraviolet irradiation was more efficient than hydrogen peroxide for decreasing chemical oxygen demand during treatment of livestock wastewater.     

Hydrogeophysical investigations in a typical khondalitic terrain to delineate the kaolinised layer using resistivity imaging

Investigation for high yielding water wells in the khondalitic terrain (graneti ferrous silliminite gnesiss) is mostly faced with the problem of identification of the extent of the depth of kaolinisation of the aquifer. The traditional Vertical Electrical Sounding survey, Seismic Refraction survey and Very Low Frequency Electromagnetic survey could not identify the kaolinisation of the aquifer in the present investigations. The Two Dimensional (2D) Resistivity and Induced Polarization (IP) Imaging surveys are attempted for the identification of kaolinised layer and depth of kaolinisation. Number of 2D Resistivity and IP Imaging profiles were conducted near Chipurupally in Vizianagaram district of Andhra Pradesh, India along successful and failed wells located within short distances. Resistivity and IP measurements were carried out using an ABEM SAS 4000 Terrameter. The resistivity and I.P. images have provided a clear view of the thickness of the highly weathered zone (kaolinised zone) at both successful and failed wells. The highly weathered zone is identified with the resistivity values below 25 ohm.m. The depth of highly weathered material at failed well is extended about 8–10 m more deeper than the successful wells at some places to as much as 20 m more deep at some other places. This extended deeper kaolinisation of the aquifer is responsible for failure of wells. Layers having resistivities between 25–65 Ohm.m are identified as aquifer layers which are composed of moderately weathered and fractured khondalitic suit of rocks (Garnti ferrous sillimanite/biotite gneiss). Layers with resistivities greater than 65 Ohm.m are interpreted to have basement characteristics belonging to the granite gneiss. Interestingly IP imaging has not provided any greater insights in delineating the kaolinistion of the aquifer when compared to resistivity Imaging, in fact resitivity imaging has shown greater depths of kaolinisation than IP Imaging.     

Constraints from melt inclusions and their host olivines on the petrogenesis of Oligocene-Early Miocene Xindian basalts, Chifeng area, North China Craton

The geochemical characteristics of melt inclusions and their host olivines provide important information on the processes that create magmas and the nature of their mantle and crustal source regions. We report chemical compositions of melt inclusions, their host olivines and bulk rocks of Xindian basalts in Chifeng area, North China Craton. Compositions of both bulk rocks and melt inclusions are tholeiitic. Based on petrographic observations and compositional variation of melt inclusions, the crystallizing sequence of Xindian basalts is as follows: olivine (at MgO > ~5.5 wt%), plagioclase (beginning at MgO = ~5.5 wt%), clinopyroxene and ilmenite (at MgO < 5.0 wt%). High Ni contents and Fe/Mn ratios, and low Ca and Mn contents in olivine phenocrysts, combining with low CaO contents of relatively high MgO melt inclusions (MgO > 6 wt%), indicate that Xindian basalts are possibly derived from a pyroxenite source rather than a peridotite source. In the CS-MS-A diagram, all the high MgO melt inclusions (MgO > 6.0 wt%) project in the field between garnet + clinopyroxene + liquid and garnet + clinopyroxene + orthopyroxene + liquid near 3.0 GPa, further suggesting that residual minerals are mainly garnet and clinopyroxene, with possible presence of orthopyroxene, but without olivine. Modeling calculations using MELTS show that the water content of Xindian basalts is 0.3–0.7 wt% at MgO = 8.13 wt%. Using 20–25 % of partial melting estimated by moderately incompatible element ratios, the water content in the source of Xindian basalts is inferred to be ≥450 ppm, much higher than 6–85 ppm in dry lithospheric mantle. The melting depth is inferred to be ~3.0 GPa, much deeper than that of tholeiitic lavas (<2.0 GPa), assuming a peridotite source with a normal mantle potential temperature. Such melting depth is virtually equal to the thickness of lithosphere beneath Chifeng area (~100 km), suggesting that Xindian basalts are derived from the asthenospheric mantle, if the lithospheric lid effect model is assumed.     

Lithosphere formation in the central Slave Craton (Canada): plume subcretion or lithosphere accretion?

Major-element compositions of minerals in peridotite xenoliths from the Lac de Gras kimberlites provide constraints on the mode of lithosphere formation beneath the central Slave Craton, Canada. Magnesia contents of reconstructed whole rocks correlate positively with NiO and negatively with CaO contents, consistent with variable partial melt extraction. Alumina and Cr₂O₃ contents are broadly positively correlated, suggestive of melt depletion in the absence of a Cr–Al phase. Garnet modes are high at a given Al₂O₃ content (a proxy for melt depletion), falling about a 7 GPa melt depletion model. These observations, combined with high olivine Mg# and major-element relationships of FeO-poor peridotites (<7.5 wt%) indicative of melt loss at pressures >3 GPa (residual FeO content being a sensitive indicator of melt extraction pressure), and similar high pressures of last equilibration (∼4.2 to 5.8 GPa), provide multiple lines of evidence that the mantle beneath the central Slave Craton has originated as a residue from high-pressure melting, possibly during plume subcretion. Apparent low melt depletion pressures for high-FeO peridotites (>7.5 wt%) could suggest formation in an oceanic setting, followed by subduction to their depth of entrainment. However, these rocks, which are characterised by low SiO₂ contents (<43 wt%), are more likely to be the result of post-melting FeO-addition, leading to spuriously low estimates of melt extraction pressures. They may have reacted with a silica-undersaturated melt that dissolved orthopyroxene, or experienced olivine injection by crystallising melts. A secular FeO-enrichment of parts of the deep mantle lithosphere is supported by lower average Mg# in xenolithic olivine (91.7) compared to olivine inclusions in diamond (92.6).     

The natural enrichment of ferruginous weathering products and its implication for water quality in the Hunchun Basin, China

In order to evaluate the extent of a natural enrichment of Fe and Mn over the whole of the Hunchun Basin, the stability of Fe-Mn mineral phases, their status, the weathering rate of source materials, and soil characteristics were determined. A variety of samples were collected from sediments, soil profiles, and surface soils. In the solutions after a sequentially selective dissolution using sodium pyrophosphate (p), acid oxalate (o), and dithionite-citrate-bicarbonate (d), Si, Al and Fe were dominant in the d and p fractions, and Mn in the o and p fractions. The results showed that the existing phases and status of Fe and Mn were distinctly different, and that the abundance of amorphous Mn phases made thermodynamic calculation difficult. An application of these ferruginous weathering products was therefore made to understand basin development. The first terrace of the Hunchun River is more active than the second terrace, which can be inferred from it having a higher value in Fe_d/Fe_t. Amorphous Fe phases such as Fe(OH)₃ and Fe₃(OH)₈ were controlling factors of Fe in the thermodynamic calculations. The transformation of the amorphous Fe phases to more stable phases was hindered by high contents of smectite and gibbsite, amorphous opaline produced from rice roots, and organic phosphate pesticides or fertilizers in soils. Source-rock deduction using water samples suggested granitic weathering. Precipitation around the Hunchun Basin is gradually becoming more acidic. Therefore, in the future it is inevitable that ecological and environmental problems related to the Fe phases mentioned above will occur in the drinking water supply for this area, especially in that of the first terrace.     

Effects of key components of <Emphasis Type="Italic">S. triqueter</Emphasis> root exudates on fractions and bioavailability of pyrene–lead co-contaminated soils

The key components of S. triqueter root exudates involved 4-oxo-pentanoic acid, succinic acid, glutaric acid, phthalate acid, citric acid, vanillic acid, myristic acid, pentadecanoic acid, decanoic acid, 14-methyl-pentadecanoic acid, hexadecanoic acid, octadecanoic acid and oleic acid, and the content of the water-soluble organic acids (citric acid, succinic acid and glutaric acid) significantly increased in pyrene and lead co-contaminated rhizosphere soil. These three water-soluble organic acids including citric acid, succinic acid and glutaric acid were detected as the specific root exudates of S. triqueter under stress of pollutants for pyrene and lead, so they were chosen as the research objects, and they were added into the bioremediation systems of pyrene and lead co-contaminated wetland soils. Compared with the control, the treatments added the three organic acids always improved the quantity of the bioavailable fraction of pyrene and lead in wetland soils and greatly influenced other chemical states of pyrene and lead fractions in the test concentration range. Under the 50 g kg^?1 of organic acids concentration, the amount of the bioavailable fraction of pyrene and lead increased 41.0 and 872.7 % by citric acid, respectively. The enhancement of bioavailability of pyrene and lead in the wetland soil by adding organic acids generally decreased in the following order: citric acid > succinic acid > glutaric acid. Enhancing effects of organic acids on the bioavailability improvement of pyrene and lead is remarkable.