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1.
In this paper, we, for the first time, report geochemistry of sandstone from Somanpalli Group from Pomburna area in the Eastern Belt of Pranhita–Godavari (PG) Valley, central India and studied to infer their provenance, intensity of paleo-weathering and depositional tectonic setting. Petrographic study of sandstones show QFL modal composition of arenite. Chemical results show high \(\hbox {SiO}_{2}\) and CIA but lower \(\hbox {Al}_{2}\hbox {O}_{3}, \hbox {TiO}_{2}\), Rb, Sr, \(\hbox {K}_{2}\hbox {O}\) indicating mixed sources. Major elements chemistry parameters such as, \(\hbox {K}_{2}\hbox {O/Al}_{2}\hbox {O}_{3}\) ratio and positive correlation of Rb with \(\hbox {K}_{2}\hbox {O}\), reflects a warm and humid climate for study area. The tectonic discrimination plots (\(\hbox {SiO}_{2}/20\)–\(\hbox {K}_{2}\hbox {O} + \hbox {Na}_{2}\hbox {O}\)–\(\hbox {TiO}_{2} + \hbox {Fe}_{2}\hbox {O}_{3} + \hbox {MgO};\,\hbox {K}_{2}\hbox {O}/\hbox {Na}_{2}\hbox {O}\) vs. \(\hbox {SiO}_{2}\); Th–Sc–Zr/20) indicate dominantly passive margin and slight active tectonic setting. Concentrations of Zr, Nb, Y, and Th are higher compared to the UCC values and the trends in Th/Cr, Th/Co, La/Sc and Cr/Zr ratios support a felsic and mafic source for these sandstones and deposition in passive margin basin. Chondrite normalized REE pattern reflects LREE depletion, negative Eu anomaly and flat HREE similar to UCC, felsic components. ICV value (0.95) also supports tectonically quiescent passive margin settings. CIA values (74) indicate high degree of chemical weathering and warm and humid paleoclimatic condition.  相似文献   

2.
The Taipusi area in the Bainaimiao Arc Belt is located in the northern margin of the North China Craton, at the southern margin of the middle Central Asian Orogenic Belt. It is characterized by large exposures of mafic dikes. In this contribution, we present first-hand whole-rock major and trace elements, zircon U–Pb geochronology and in situ trace element geochemistry data for these mafic rocks, which reveal their petrogenesis and tectonic evolution. These mafic dikes display varied compositions of \(\hbox {SiO}_{2}\) (49.42–54.29%), \(\hbox {TiO}_{2}\) (0.63–1.08%), \(\hbox {Al}_{2}\hbox {O}_{3}\) (13.94–17.60%), MgO (4.66–10.51%), \(\hbox {Fe}_{2}\hbox {O}_{3}\) (1.59–3.07%), FeO (4.60–6.90%), CaO (4.57–8.91%), \(\hbox {Na}_{2}\hbox {O}\) (1.61–4.26%), \(\hbox {K}_{2}\hbox {O}\) (0.92–2.54%) and \(\hbox {P}_{2}\hbox {O}_{5}\) (0.11–0.29%). They are mainly of high-K calc-alkaline series with indistinct Eu anomalies, enriched in large ion lithophile elements (e.g., Rb, Ba, K and Sr) but depleted in high field strength elements (e.g., Nb, P and Ti). These suggest that the crystallizing magma was derived from enriched mantle altered by metasomatic fluids in a subduction setting with imprints of active continental margin features. The high concentrations of Hf, U, Th, Pb and Y, pronounced positive Ce but slightly negative Eu anomalies in zircons indicating that the magma underwent a fractional crystallization and crustal contamination process, with medium to high \(f\hbox {O}_{2}\). Zircon LA–ICP–MS U–Pb dating yielded concordant ages of 437–442 Ma for these mafic dikes, which is consistent with the early Paleozoic volcanic arc magmatic activity in the Bainaimiao area. Hence, we conclude that the Bainaimiao Arc Belt is a continental arc formed by the southward subduction of the Paleo-Asian ocean during early Paleozoic.  相似文献   

3.
In the present study, measurements of surface ozone (\(\hbox {O}_{3}\)) and its precursors (NO and \(\hbox {NO}_{2}\)) were carried out at a sub-urban site of Agra (\(27{^{\circ }}10'\hbox {N}\), \(78{^{\circ }}05'\hbox {E}\)), India during May 2012–May 2013. During the study period, average concentrations of \(\hbox {O}_{3}\), NO, and \(\hbox {NO}_{2}\) were \(39.6 \pm 25.3\), \(0.8 \pm 0.8\) and \(9.1 \pm 6.6 \, \hbox {ppb}\), respectively. \(\hbox {O}_{3}\) showed distinct seasonal variation in peak value of diurnal variation: summer \({>}\) post-monsoon \({>}\) winter \({>}\) monsoon. However, \(\hbox {NO}_{2}\) showed highest levels in winter and lowest in monsoon. The average positive rate of change of \(\hbox {O}_{3}\) (08:00–11:00 hr) was highest in April (16.3 ppb/hr) and lowest in August (1.1 ppb/hr), while average negative rate of change of \(\hbox {O}_{3}\) (17:00–19:00 hr) was highest in December (–13.2 ppb/hr) and lowest in July (–1.1 ppb/hr). An attempt was made to identify the \(\hbox {VOC--NO}_{\mathrm{x}}\) sensitivity of the site using \(\hbox {O}_{3}/\hbox {HNO}_{3}\) ratio as photochemical indicator. Most of the days this ratio was above the threshold value (12–16), which suggests \(\hbox {NO}_{\mathrm{x}}\) sensitivity of the site. The episodic event of ozone was characterized through meteorological parameters and precursors concentration. Fine particles (\(\hbox {PM}_{2.5}\)) cause loss of ozone through heterogeneous reactions on their surface and reduction in solar radiation. In the study, statistical analyses were used to estimate the amount of ozone loss.  相似文献   

4.
The phonon dispersion and thermodynamic properties of pyrope (\(\hbox {Mg}_3\hbox {Al}_2\hbox {Si}_3\hbox {O}_{12}\)) and grossular (\(\hbox {Ca}_3\hbox {Al}_2\hbox {Si}_3\hbox {O}_{12}\) ) have been computed by using an ab initio quantum mechanical approach, an all-electron variational Gaussian-type basis set and the B3LYP hybrid functional, as implemented in the Crystal program. Dispersion effects in the phonon bands have been simulated by using supercells of increasing size, containing 80, 160, 320, 640, 1280 and 2160 atoms, corresponding to 1, 2, 4, 8, 16 and 27 \(\mathbf {k}\) points in the first Brillouin zone. Phonon band structures, density of states and corresponding inelastic neutron scattering spectra are reported. Full convergence of the various thermodynamic properties, in particular entropy (S) and specific heat at constant volume (\(C_\mathrm{{V}}\)), with the number of \(\mathbf {k}\) points is achieved with 27 \(\mathbf {k}\) points. The very regular behavior of the S(T) and \(C_\mathrm{{V}}(T)\) curves as a function of the number of \(\mathbf {k}\) points, determined by high numerical stability of the code, permits extrapolation to an infinite number of \(\mathbf {k}\) points. The limiting value differs from the 27-\(\mathbf {k}\) case by only 0.40 % at 100 K for S (the difference decreasing to 0.11 % at 1000 K) and by 0.29 % (0.05 % at 1000 K) for \(C_\mathrm{{V}}\). The agreement with the experimental data is rather satisfactory. We also address the problem of the relative entropy of pyrope and grossular, a still debated question. Our lattice dynamical calculations correctly describe the larger entropy of pyrope than grossular by taking into account merely vibrational contributions and without invoking “static disorder” of the Mg ions in dodecahedral sites. However, as the computed entropy difference is found to be larger than the experimental one by a factor of 2–3, present calculations cannot exclude possible thermally induced structural changes, which could lead to further conformational contributions to the entropy.  相似文献   

5.
The eddy covariance method is a powerful technique for quantification of \(\hbox {CO}_{2},\) \(\hbox {H}_{2}\)O and energy fluxes in natural ecosystems. Leaf area index (LAI) and its changes are significant drivers of \(\hbox {CO}_{2}\) and \(\hbox {H}_{2}\)O exchange in a forest ecosystem due to their role in photosynthesis. The present study reports the seasonal variation of \(\hbox {CO}_{2}\) and energy fluxes and their relationship with other meteorological parameters of a semi-evergreen primary forest of Kaziranga National Park, Assam, India during February 2016–January 2017. The diurnal pattern of half hourly average \(\hbox {CO}_{2 }\) fluxes over the forest was found to be mostly dominated by the incident photosynthetically active radiation. During the period of study, diurnal variations of \(\hbox {CO}_{2}\) flux showed a maximum value of \(-9.97\,\upmu \)mol \(\hbox {m}^{-2}\hbox {s}^{-1}\) in the month of June during summer which is also the beginning of the monsoon season. The monthly averaged diurnal \(\hbox {CO}_{2}\) flux and variation in LAI of the forest canopy closely followed each other. The annual net ecosystem exchange of the forest estimated from the \(\hbox {CO}_{2}\) flux data above the canopy is 84.21 g C \(\hbox {m}^{-2}\,\hbox {yr}^{-1}\). Further studies are in progress to confirm these findings. The estimated average annual evapotranspiration of the semi-evergreen forest is 2.8 ± 0.19 mm \(\hbox {day}^{-1}\). The study of partitioning of energy fluxes showed the dominance of latent heat fluxes over sensible heat fluxes. The energy balance closure was found to increase with an increase in instability and the highest closure of around 83% was noted under neutral conditions.  相似文献   

6.
Stable isotopes of benthic foraminifera have widely been applied in micropalaeontological research to understand vital effects in foraminifera. Isotopic fractionations are mainly controlled by ontogeny, bottom/pore water chemistry, habitat preference, kinetic effect and respiration. Discontinuous abundance of a species for isotopic analysis has forced us to select multiple species from down-core samples. Thus standardisation factors are required to convert isotopic values of one species with respect to other species. The present study is pursued on isotopic values of different pairs of benthic foraminifera from the Krishna–Godavari basin and Peru offshore to understand habitat-wise isotopic variation and estimation of isotopic correction factors for the paired species (Cibicides wuellerstorfi–Bulimina marginata, Ammonia spp.–Loxostomum amygdalaeformis and Bolivina seminuda–Nonionella auris). Infaunal species (B. marginata, Ammonia spp. and N. auris) show a lighter carbon isotopic excursion with respect to the epifaunal to shallow infaunal forms (C. wuellerstorfi, L. amygdalaeformis and B. seminuda). These lighter \(\updelta ^{13}\) \(\hbox {C}\) values are related to utilisation of \(\hbox {CO}_{2}\) produced by anaerobic remineralisation of organic matter. However, enrichment of \(\updelta ^{18}\) \(\hbox {O}\) for the deeper microhabitat (bearing lower pH and decreased \({\hbox {CO}_{3}}^{2-})\) is only recorded in case of B. marginata. It is reverse in case of N. auris and related to utilisation of respiratory \(\hbox {CO}_{2}\) and internal dissolve inorganic carbon pool. Estimation of interspecies isotopic correction factors for the species pairs (\(\updelta ^{13}\) \(\hbox {C}\) of C. wuellerstorfi–B. marginata, L. amygdalaeformis–Ammonia spp., N. auris–B. seminuda) and \(\updelta ^{18}\) \(\hbox {O}\) of C. wuellerstorfi–B. marginata are statistically reliable and may be used in palaeoecological studies.  相似文献   

7.
We calculated the phase diagram of \(\hbox {AlPO}_{4}\) up to 15 GPa and 2,000 K and investigated the thermodynamic properties of the high-pressure phases. The investigated phases include the berlinite, moganite-like, \(\hbox {AlVO}_{4},\, P2_1/c\), and \(\hbox {CrVO}_{4}\) phases. The computational methods used include density functional theory, density functional perturbation theory, and the quasiharmonic approximation. The investigated thermodynamic properties include the thermal equation of state, isothermal bulk modulus, thermal expansivity, and heat capacity. With increasing pressure, the ambient phase berlinite transforms to the moganite-like phase, and then to the \(\hbox {AlVO}_{4}\) and \(P2_1/c\) phases, and further to the \(\hbox {CrVO}_{4}\) phase. The stability fields of the \(\hbox {AlVO}_{4}\) and \(P2_1/c\) phases are similar in pressure but different in temperature, as the \(\hbox {AlVO}_{4}\) phase is stable at low temperatures, whereas the \(P2_1/c\) phase is stable at high temperatures. All of the phase relationships agree well with those obtained by quench experiments, and they support the stabilities of the moganite-like, \(\hbox {AlVO}_{4}\), and \(P2_1/c\) phases, which were not observed in room-temperature compression experiments.  相似文献   

8.
This paper describes the development of a new Near InfraRed Imaging Spectrograph (NIRIS) which is capable of simultaneous measurements of OH(6-2) Meinel and \(\hbox {O}_{2}\)(0-1) atmospheric band nightglow emission intensities. In this spectrographic technique, rotational line ratios are obtained to derive temperatures corresponding to the emission altitudes of 87 and 94 km. NIRIS has been commissioned for continuous operation from optical aeronomy observatory, Gurushikhar, Mount Abu (\(24.6^{\circ }\hbox {N}\), \(72.8^{\circ }\hbox {E}\)) since January 2013. NIRIS uses a diffraction grating of 1200 lines \(\hbox {mm}^{-1}\) and 1024\(\times \)1024 pixels thermoelectrically cooled CCD camera and has a large field-of-view (FOV) of \(80^{\circ }\) along the slit orientation. The data analysis methodology adopted for the derivation of mesospheric temperatures is also described in detail. The observed NIRIS temperatures show good correspondence with satellite (SABER) derived temperatures and exhibit both tidal and gravity waves (GW) like features. From the time taken for phase propagation in the emission intensities between these two altitudes, vertical phase speed of gravity waves, \(c_{z}\), is calculated and along with the coherent GW time period ‘\(\tau \)’, the vertical wavelength, \(\lambda _{z}\), is obtained. Using large FOV observations from NIRIS, the meridional wavelengths, \(\lambda _{y}\), are also calculated. We have used one year of data to study the possible cause(s) for the occurrences of mesospheric temperature inversions (MTIs). From the statistics obtained for 234 nights, it appears that in situ chemical heating is mainly responsible for the observed MTIs than the vertical propagation of the waves. Thus, this paper describes a novel near infrared imaging spectrograph, its working principle, data analysis method for deriving OH and \(\hbox {O}_{2}\) emission intensities and the corresponding rotational temperatures at these altitudes, derivation of gravity wave parameters (\(\tau \), \(c_{z}\), \(\lambda _{z}\), and \(\lambda _{y})\), and results on the statistical study of MTIs that exist in the earth’s mesospheric altitudes.  相似文献   

9.
This systematic study was carried out with objective to delineate the various sources responsible for \(\hbox {NO}_{3}^{-}\) contamination and \(\hbox {F}^{-}\) enrichment by utilizing statistical and graphical methods. Since Central Ground Water Board, India, indicated susceptibility of \(\hbox {NO}_{3}^{-}\) contamination and \(\hbox {F}^{-}\) enrichment, in most of the groundwater, \(\hbox {NO}_{3}^{-}\) and \(\hbox {F}^{-}\) concentration primarily observed \({>}45\) and \({>}1.5~\hbox {mg/L}\), respectively, i.e., higher than the permissible limit for drinking water. Water Quality Index (WQI) indicates \({\sim }22.81\%\) groundwater are good-water, \({\sim }71.14\%\) groundwater poor-water, \({\sim }5.37\%\) very poor-water and 0.67% unsuitable for drinking purpose. Piper diagram indicates \({\sim }59.73\%\) groundwater hydrogeochemical facies are Ca–Mg–\(\hbox {HCO}_{3 }\) water-types, \({\sim }28.19\%\) Ca–Mg–\(\hbox {SO}_{4}\)–Cl water-types, \({\sim }8.72\%\) Na–K–\(\hbox {SO}_{4}\)–Cl water-types and 3.36% Na–K–\(\hbox {HCO}_{3 }\) water-types. This classification indicates dissolution and mixing are mainly controlling groundwater chemistry. Salinity diagram indicate \({\sim }44.30\%\) groundwater under in low sodium and medium salinity hazard, \({\sim }49.66\%\) groundwater fall under low sodium and high salinity hazard, \({\sim }3.36\%\) groundwater fall under very-high salinity hazard. Sodium adsorption ratio indicates \({\sim }97\%\) groundwater are in excellent condition for irrigation. The spatial distribution of \(\hbox {NO}_{3}^{-}\) indicates significant contribution of fertilizer from agriculture lands. Fluoride enrichment occurs in groundwater through the dissolution of fluoride-rich minerals. By reducing the consumption of fertilizer and stress over groundwater, the water quality can be improved.  相似文献   

10.
The present work deals with the generations of Fe–Ti oxides and the variation in magnetic fabrics of the Dalma lavas and associated meta-sediments of the Singhbhum Mobile Belt (SMB) in relation to tectonics. Generations of the Fe–Ti oxides are different in meta-sediments and volcanics, the former preserving upliftment related oxidised grains, whereas the latter contains fresh grains prompting towards their upliftment due to plume upwelling before the volcanic eruption. In the meta-sediments, the magnetic fabric has close accordance with \(\hbox {D}_{2}/\hbox {F}_{2}\) event revealing synchronous development with \(\hbox {D}_{2}\). The Dalma thrust developed a sudden break in the homogeneity of the magnetic fabrics of the rocks where the magnetic foliations are all parallel to the Dalma thrust. This also causes \(P_{j}\) to be highest in this sector. The magnetic fabrics of volcanic rocks are different from the meta-sediments and record no signature of deformation. The pattern of distribution of susceptibility axes are in accordance with the subaerial lava flows. However, their \(\hbox {K}_{1}\) and \(\hbox {K}_{2}\) dispersed throughout the periphery with \(\hbox {K}_{3}\) clustering at the centre. This infers towards the fact that although the volcanism took place in a subaerial environment, calm aqueous environment was locally present where the oblate grains settled on the eruption surface with their \(\hbox {K}_{3}\) vertical.  相似文献   

11.
Crystallochemical data on metamict davidite from albitites and albitised rocks from the Bichun area (Jaipur district, Rajasthan, India) of Banded Gneissic Complex (BGC) are provided. Davidite occurs as euhedral, subhedral to anhedral crystals in the form of disseminated grains and also as fracture filled veins. The crystals of davidite are up to 8 cm in length and 6 cm in width. The powder X-ray diffraction (XRD) pattern of the heat-treated davidite (at \(900{^{\circ }}\hbox {C}\)) reveals well-defined reflections of crystallographic planes. The calculated unit-cell parameters of the heat treated davidite are: \(\hbox {a}_{0} = \hbox {b}_{0} = 10.3556 \, \text {\AA }\) and \(\hbox {c}_{0} = 20.9067 \, \text {\AA }\), with unit-cell volume \(\hbox {(V)} = 1941.6385 \, \text {\AA }^{3}\); and \({\upalpha }={\upbeta }= 90^{\circ }\) and \({\upgamma }= 120^{\circ }\), which are in agreement with the values of davidite standard. Geochemical data reveals that the investigated davidite contains 51.5–52.6% \(\hbox {TiO}_{2}\), 14.8–15.1% \(\hbox {Fe}_{2} \hbox {O}_{3}\), 9.8–10.2% FeO, 6.97–7.12% \(\hbox {U}_{3} \hbox {O}_{8}\), 6.72–6.92% \(\hbox {RE}_{2} \hbox {O}_{3}\), 3.85–3.61% \(\hbox {K}_{2}\hbox {O}\), 0.9–1.4% \(\hbox {Al}_{2} \hbox {O}_{3}\), and 0.8–1.2% \(\hbox {SiO}_{2}\). The calculated structural formulae of the two davidite crystals are: D-1: \(\hbox {K}_{0.0044/0.004} \hbox {Ba}_{0.0044/0.005} \hbox {Ca}_{0.20/0.20} \hbox {Na}_{0.012/0.012} \hbox {Mn}_{0.053/0.053} \hbox {Mg}_{0.14/0.14} \hbox {Pb}_{0.0076/0.008} \hbox {Fe}_{2.675/2.675} \hbox {Fe}_{1.59/1.59} \hbox {Y}_{0.1175/0.118} \hbox {P}_{0.053/0.053} \hbox {Nb}_{0.008/0.008} \hbox {Sn}_{0.001/0.001} \hbox {Zr}_{0.033/0.033} \hbox {U}_{0.468/0.468} \hbox {Th}_{0.009/0.009} \,\,\hbox {REE}_{0.6829/0.683})_{6.05/6.05} (\hbox {Ti}_{12.15/12.15}\,\, \hbox {Fe}_{1.9022/1.903} \hbox {Si}_{0.372/0.372}\,\, \hbox {Al}_{0.517/0.517}\,\, \hbox {Cr}_{0.018/0.018} \hbox {Co}_{0.009/0.009} \hbox {Ni}_{0.027/0.027})_{15/15} \hbox {O}_{36/36} (\hbox {OH}_{0.319/0.319[]1.681/1.681})_{2/2}\) and D-2: \((\hbox {K}_{0.004/0.004} \hbox {Ba}_{0.005/0.005} \hbox {Ca}_{0.20/0.20} \hbox {Na}_{0.012/0.012} \hbox {Mn}_{0.05/0.05} \hbox {Mg}_{0.094/0.094} \hbox {Pb}_{0.007/0.007} \hbox {Fe}_{2.58/2.58} \hbox {Fe}_{1.71/1.71} \hbox {Y}_{0.112/0.112} \hbox {P}_{0.106/0.106} \hbox {Nb}_{0.006/0.006} \hbox {Sn}_{0.001/0.001} \hbox {Zr}_{0.03/0.03} \hbox {U}_{0.48/0.48} \hbox {Th}_{0.009/0.009} \hbox {REE}_{0.665/0.665})_{6.088/6.088} (\hbox {Ti}_{12.48/12.48} \hbox {Fe}_{1.87/1.87} \hbox {Si}_{0.249/0.249} \hbox {Al}_{0.334/0.334} \hbox {Cr}_{0.019/0.019} \hbox {Co}_{0.008/0.008} \hbox {Ni}_{0.04/0.04})_{15/15} \hbox {O}_{36/36} (\hbox {OH}_{0.098/0.098[]1.90/1.90})_{2/2}\). The calculated structural formulae are not fully stoichiometric, which could be due to metamict nature of davidite. The characteristic feature of distribution pattern of REE in davidite is unusually high concentration of LREE and HREE and substantially low content of MREE. It may be due to the occupation of REEs in two distinct crystallographic sites in davidite structure, i.e., M(1) and M(O) sites. Chondrite-normalised plot of davidite reveals a pronounced negative Eu-anomaly (\(\hbox {Eu}/\hbox {Eu}^{*} = 0.30{-}0.39\)), which suggests extremely fractionated nature of the metasomatising fluids from which davidite had crystallized. Metamict davidite-bearing U ores not only from Rajasthan, but also from other parts of India are likely to yield very high U leachability, thereby making them attractive sources of U, which otherwise are ignored by mineral engineers as uneconomic U ores.  相似文献   

12.
Oxygen (\({\updelta }^{18}\hbox {O}\)) and hydrogen (\({\updelta }^{2}\hbox {H}\) and \(^{3}\hbox {H}\)) isotopes of water, along with their hydrochemistry, were used to identify the source of a newly emerged seepage water in the downstream of Lake Nainital, located in the Lesser Himalayan region of Uttarakhand, India. A total of 57 samples of water from 19 different sites, in and around the seepage site, were collected. Samples were analysed for chemical tracers like \(\hbox {Ca}^{++}\), \(\hbox {Mg}^{++}\), \(\hbox {Na}^{+}\), \(\hbox {K}^{+}\), \({\hbox {SO}_{4}}^{--}\) and \(\hbox {Cl}^{-}\) using an Ion Chromatograph (Dionex IC-5000). A Dual Inlet Isotope Ratio Mass Spectrometer (DIIRMS) and an Ultra-Low Level Liquid Scintillation Counter (ULLSC), were used in measurements of stable isotopes (\({\updelta }^{2}\hbox {H}\) and \({\updelta }^{18}\hbox {O}\)) and a radioisotope (\(^{3}\hbox {H}\)), respectively. Results obtained in this study repudiate the possibility of any likely connection between seepage water and the lake water, and indicate that the source of seepage water is mainly due to locally recharged groundwater. The study suggests that environmental isotopes (\({\updelta }^{2}\hbox {H}\), \({\updelta }^{18}\hbox {O}\) and \(^{3}\hbox {H}\)) can effectively be used as ‘tracers’ in the detection of the source of seepage water in conjunction with other hydrochemical tracers, and can help in water resource management and planning.  相似文献   

13.
The fluvial geochemistry of the Subarnarekha River and its major tributaries has been studied on a seasonal basis in order to assess the geochemical processes that explain the water composition and estimate solute fluxes. The analytical results show the mildly acidic to alkaline nature of the Subarnarekha River water and the dominance of \(\hbox {Ca}^{2+}\) and \(\hbox {Na}^{+}\) in cationic and \(\hbox {HCO}_{3}^{-}\) and \({\hbox {Cl}}^{-}\) in anionic composition. Minimum ionic concentration during the monsoon and maximum concentration in the pre-monsoon seasons reflect concentrating effects due to decrease in the river discharge and increase in the base flow contribution during the pre-monsoon and dilution effects of atmospheric precipitation in the monsoon season. The solute acquisition processes are mainly controlled by weathering of rocks, with minor contribution from marine and anthropogenic sources. Higher contribution of alkaline earth \((\hbox {Ca}^{2+}{+}\,\hbox {Mg}^{2+})\) to the total cations \((\hbox {TZ}^{+})\) and high \((\hbox {Na}^{+}+\hbox {K}^{+})/\hbox {Cl}^{-}\), \((\hbox {Na}^{+}+\hbox {K}^{+})/\hbox {TZ}^{+}\), \(\hbox {HCO}_{3}^{-}/(\hbox {SO}_{4}^{2-}+\hbox {Cl}^{-})\) and low \((\hbox {Ca}^{2+}+\hbox {Mg}^{2+})/(\hbox {Na}^{+}+\hbox {K}^{+})\) equivalent ratios suggest that the Subarnarekha River water is under the combined influence of carbonate and silicate weathering. The river water is undersaturated with respect to dolomite and calcite during the post-monsoon and monsoon seasons and oversaturated in the pre-monsoon season. The pH–log \(\hbox {H}_{4}\hbox {SiO}_{4}\) stability diagram demonstrates that the water chemistry is in equilibrium with the kaolinite. The Subarnarekha River annually delivered \(1.477\times 10^{6}\) ton of dissolved loads to the Bay of Bengal, with an estimated chemical denudation rate of \(77\hbox { ton km}^{-2}\hbox { yr}^{-1}\). Sodium adsorption ratio, residual sodium carbonate and per cent sodium values placed the studied river water in the ‘excellent to good quality’ category and it can be safely used for irrigation.  相似文献   

14.
The structural and spectroscopic characteristics of phosphatic ferruginous shale samples from the Bijawar Group rocks from Sagar District of Madhya Pradesh (India) have been probed for identification of uranium species. Fluorapatite (\(\hbox {Ca}_{5}\hbox {(PO}_{4})_{3}\hbox {F}\), FAP) and haematite (\(\upalpha \)-\(\hbox {Fe}_{2}\hbox {O}_{3}\)) were identified as the main phases in the separated mineral concentrates. The photoluminescence (PL) and X-ray absorption near edge spectroscopy (XANES) studies pointed to a strong experimental evidence of both U(IV) and U(VI) oxidation states in the mineral concentrate portion obtained from the same parent host rock. The PL spectrum has confirmed the charge transfer (f–d) transition bands in UV and near-UV regions with emission peaks at ca. 290, 313, 336, 399 and 416 nm, which has been attributed to the substitution of \(\hbox {Ca}^{2+}\) ions by U(IV) in FAP and broad structureless emission due to stabilisation of U(VI) as \(\hbox {UO}_{6}^{6-}\) in haematite. Time-resolved spectroscopy studies have revealed biexponential decay components lasting 2–5 ns for U(IV) species and \(10\,\upmu \hbox {s}\) for U(VI) species. These characterisations revealed the fundamental information about the oxidation state and form of uranium in this region. Remediation measures for the Bijawar region are also suggested.  相似文献   

15.
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16.
Tonalite–trondhjemite–granodiorite gneisses (TTG) and K-rich granites are extensively exposed in the Mesoarchean to Paleoproterozoic Bundelkhand craton of central India. The TTGs rocks are coarse- grained with biotite, plagioclase feldspar, K-feldspar and amphibole as major constituent phases. The major minerals constituting the K-rich granites are K-feldspar, plagioclase feldspar and biotite. They are also medium to coarse grained. Mineral chemical studies show that the amphiboles of TTG are calcic amphibole hastingsite, plagioclase feldspars are mostly of oligoclase composition, K-feldspars are near pure end members and biotites are solid solutions between annite and siderophyllite components. The K-rich granites have biotites of siderophyllite–annite composition similar to those of TTGs, plagioclase feldspars are oligoclase in composition, potassic feldspars have \(\hbox {X}_{\mathrm{K}}\) ranging from 0.97 to 0.99 and are devoid of any amphibole. The tonalite–trondhjemite–granodiorite gneiss samples have high \(\hbox {SiO}_{2}\) (64.17–74.52 wt%), \(\hbox {Na}_{2}\hbox {O}\) (3.11–5.90 wt%), low Mg# (30–47) and HREE contents, with moderate \((\hbox {La/Yb})_{\mathrm{CN}}\) values (14.7–33.50) and Sr/Y ratios (4.85–98.7). These geochemical characteristics suggest formation of the TTG by partial melting of the hydrous basaltic crust at pressures and depths where garnet and amphibole were stable phases in the Paleo-Mesoarchean. The K-rich granite samples show high \(\hbox {SiO}_{2}\) (64.72–76.73 wt%), \(\hbox {K}_{2}\hbox {O}\) (4.31–5.42), low \(\hbox {Na}_{2}\hbox {O}\) (2.75–3.31 wt%), Mg# (24–40) and HREE contents, with moderate to high \((\hbox {La/Yb})_{\mathrm{CN}}\) values (9.26–29.75) and Sr/Y ratios (1.52–24). They differ from their TTG in having elevated concentrations of incompatible elements like K, Zr, Th, and REE. These geochemical features indicate formation of the K-granites by anhydrous partial melting of the Paleo-Mesoarchean TTG or mafic crustal materials in an extensional regime. Combined with previous studies it is interpreted that two stages of continental accretion (at 3.59–3.33 and 3.2–3.0 Ga) and reworking (at 2.5–1.9 Ga) occurred in the Bundelkhand craton from Archaean to Paleoproterozoic.  相似文献   

17.
Shallow aquifer vulnerability has been assessed using GIS-based DRASTIC model by incorporating the major geological and hydrogeological factors that affect and control the groundwater contamination in a granitic terrain. It provides a relative indication of aquifer vulnerability to the contamination. Further, it has been cross-verified with hydrochemical signatures such as total dissolved solids (TDS), \(\hbox {Cl}^{-},\, \hbox {HCO}_{3}^{-},\, \hbox {SO}_{4}^{2-}\) and \(\hbox {Cl}^{-}/\hbox {HCO}_{3}^{-}\) molar ratios. The results show four zones of aquifer vulnerability (i.e., negligible, low, moderate and high) based on the variation of DRASTIC Vulnerability Index (DVI) between 39 and 132. About 57% area in the central part is found moderately and highly contaminated due to the 80 functional tannery disposals and is more prone to groundwater aquifer vulnerability. The high range values of TDS (2304–39,100 mg/l); \(\hbox {Na}^{+}\)(239– 6,046 mg/l) and \(\hbox {Cl}^{-}\) (532–13,652 mg/l) are well correlated with the observed high vulnerable zones. The values of \(\hbox {Cl}^{-}/\hbox {HCO}_{3}^{-}\) (molar ratios: 1.4–106.8) in the high vulnerable zone obviously indicate deterioration of the aquifer due to contamination. Further cumulative probability distributions of these parameters indicate several threshold values which are able to demarcate the diverse vulnerability zones in granitic terrain.  相似文献   

18.
The deglacial transition from the last glacial maximum at \(\sim \)20 kiloyears before present (ka) to the Holocene (11.7 ka to Present) was interrupted by millennial-scale cold reversals, viz., Antarctic Cold Reversal (\(\sim \)14.5–12.8 ka) and Greenland Younger Dryas (\(\sim \)12.8–11.8 ka) which had different timings and extent of cooling in each hemisphere. The cause of this synchronously initiated, but different hemispheric cooling during these cold reversals (Antarctic Cold Reversal \(\sim \)3\(^{\circ }\hbox {C}\) and Younger Dryas \(\sim \)10\(^{\circ }\hbox {C}\)) is elusive because \(\hbox {CO}_{2}\), the fundamental forcing for deglaciation, and Atlantic meridional overturning circulation, the driver of antiphased bipolar climate response, both fail to explain this asymmetry. We use centennial-resolution records of the local surface water \(\delta ^{18}\hbox {O}\) of the Eastern Arabian Sea, which constitutes a proxy for the precipitation associated with the Indian Summer Monsoon, and other tropical precipitation records to deduce the role of tropical forcing in the polar cold reversals. We hypothesize a mechanism for tropical forcing, via the Indian Summer Monsoons, of the polar cold reversals by migration of the Inter-Tropical Convergence Zone and the associated cross-equatorial heat transport.  相似文献   

19.
The effect of solar flare, sudden commencement of magnetic storm and of the disturbances ring current on the equatorial electrojet in the Eastern Brazil region, where the ground magnetic declination is as large as \(20^{^{\circ }}\hbox {W}\) is studied based on geomagnetic data with one minute resolution from Bacabal during November–December 1990. It is shown that the mean diurnal vector of the horizontal field was aligned along \(2{^{\circ }}\hbox {E}\) of north at Huancayo and \(30{^{\circ }}\hbox {W}\) of north at Bacabal during the month of December 1990. Number of solar flares that occurred on 30 December 1990 indicated the direction of solar flare related \(\Delta H\) vector to be aligned along \(5{^{\circ }}\hbox {E}\) of north at Huancayo and \(28{^{\circ }}\hbox {W}\) of north at Bacabal. This is expected as the solar flare effects are due to the enhanced conductivity in the ionosphere. The SC at 2230 UT on 26 November 1990 produced a positive impulse in \(\Delta X\) and negative impulse in \(\Delta Y\) at Bacabal with \(\Delta H\) vector aligned along \(27{^{\circ }}\hbox {W}\) of north. At Huancayo the \(\Delta H\) vector associated with SC is aligned along \(8{^{\circ }}\hbox {E}\) of north, few degrees east to the alignment of the diurnal vector of H. The magnetic storm that followed the SC had a minimum Dst index of –150 nT. The corresponding storm time disturbance in \(\Delta X\) at Huancayo as well as at Bacabal were about –250 nT but \(\Delta Y\) at Bacabal was about +70 nT and very small at Huancayo, that give the alignment of the H vector due to ring current about \(16{^{\circ }}\hbox {W}\) of north at Bacabal and almost along N–S at Huancayo. Thus alignment of the \(\Delta H\) vector due to ring current at Bacabal is \(14{^{\circ }}\hbox {E}\) of the mean direction of \(\Delta H\) vector during December 1990. This is consistent with the direction of ring current dependent on the dipole declination at the ring current altitude which is about \(5{^{\circ }}\hbox {W}\) of north over Bacabal and the deviation of declination due to the ring current during disturbed period given by the angle (\(\psi \)-D).  相似文献   

20.
We present a spectroscopic study of the iron \(\hbox{M}_{2/3}\)-edge for several minerals and compounds to reveal information about the oxidation state and the local coordination of iron. We describe a novel approach to probe the iron \(\hbox{M}_{2/3}\)-edge bulk sensitively using X-ray Raman scattering. Significant changes in the onset and shape of the Fe \(\hbox{M}_{2/3}\)-edge were observed on ferrous and ferric model compounds with Fe in octahedral and tetrahedral coordination. Simulation of the spectra is possible using an atomic multiplet code, which potentially allows determination of, e.g., crystal-field parameters in a quantitative manner. A protocol is discussed for determination of the Fe oxidation state in compounds by linear combination of spectra of ferric and ferrous end members. The presented results demonstrate the capabilities of Fe \(\hbox{M}_{2/3}\)-edge spectroscopy by X-ray Raman scattering to extract information on the ratio of trivalent to total iron \(\hbox{Fe}^{3+}/\sum \hbox{Fe}\) and local coordination. As X-ray Raman scattering is performed with hard X-rays, this approach is suitable for in situ experiments at high pressure and temperature. It thus may provide indispensable information on oxidation state, electronic structure and local structure of materials that are important for physical and chemical processes of the deep Earth.  相似文献   

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