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1.
We have estimated soil moisture (SM) by using circular horizontal polarization backscattering coefficient (\(\sigma ^{\mathrm{o}}_{\mathrm{RH}}\)), differences of circular vertical and horizontal \(\sigma ^{\mathrm{o}} \, (\sigma ^{\mathrm{o}}_{\mathrm{RV}} {-} \sigma ^{\mathrm{o}}_{\mathrm{RH}})\) from FRS-1 data of Radar Imaging Satellite (RISAT-1) and surface roughness in terms of RMS height (\({\hbox {RMS}}_{\mathrm{height}}\)). We examined the performance of FRS-1 in retrieving SM under wheat crop at tillering stage. Results revealed that it is possible to develop a good semi-empirical model (SEM) to estimate SM of the upper soil layer using RISAT-1 SAR data rather than using existing empirical model based on only single parameter, i.e., \(\sigma ^{\mathrm{o}}\). Near surface SM measurements were related to \(\sigma ^{\mathrm{o}}_{\mathrm{RH}}\), \(\sigma ^{\mathrm{o}}_{\mathrm{RV}} {-} \sigma ^{\mathrm{o}}_{\mathrm{RH}}\) derived using 5.35 GHz (C-band) image of RISAT-1 and \({\hbox {RMS}}_{\mathrm{height}}\). The roughness component derived in terms of \({\hbox {RMS}}_{\mathrm{height}}\) showed a good positive correlation with \(\sigma ^{\mathrm{o}}_{\mathrm{RV}} {-} \sigma ^{\mathrm{o}}_{\mathrm{RH}} \, (R^{2} = 0.65)\). By considering all the major influencing factors (\(\sigma ^{\mathrm{o}}_{\mathrm{RH}}\), \(\sigma ^{\mathrm{o}}_{\mathrm{RV}} {-} \sigma ^{\mathrm{o}}_{\mathrm{RH}}\), and \({\hbox {RMS}}_{\mathrm{height}}\)), an SEM was developed where SM (volumetric) predicted values depend on \(\sigma ^{\mathrm{o}}_{\mathrm{RH}}\), \(\sigma ^{\mathrm{o}}_{\mathrm{RV}} {-} \sigma ^{\mathrm{o}}_{\mathrm{RH}}\), and \({\hbox {RMS}}_{\mathrm{height}}\). This SEM showed \(R^{2}\) of 0.87 and adjusted \(R^{2}\) of 0.85, multiple R=0.94 and with standard error of 0.05 at 95% confidence level. Validation of the SM derived from semi-empirical model with observed measurement (\({\hbox {SM}}_{\mathrm{Observed}}\)) showed root mean square error (RMSE) = 0.06, relative-RMSE (R-RMSE) = 0.18, mean absolute error (MAE) = 0.04, normalized RMSE (NRMSE) = 0.17, Nash–Sutcliffe efficiency (NSE) = 0.91 (\({\approx } 1\)), index of agreement (d) = 1, coefficient of determination \((R^{2}) = 0.87\), mean bias error (MBE) = 0.04, standard error of estimate (SEE) = 0.10, volume error (VE) = 0.15, variance of the distribution of differences \(({\hbox {S}}_{\mathrm{d}}^{2}) = 0.004\). The developed SEM showed better performance in estimating SM than Topp empirical model which is based only on \(\sigma ^{\mathrm{o}}\). By using the developed SEM, top soil SM can be estimated with low mean absolute percent error (MAPE) = 1.39 and can be used for operational applications.  相似文献   

2.
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   

3.
We report the results of experiments designed to separate the effects of temperature and pressure from liquid composition on the partitioning of Ni between olivine and liquid, \(D_{\text{Ni}}^{\text{ol/liq}}\). Experiments were performed from 1300 to 1600 °C and 1 atm to 3.0 GPa, using mid-ocean ridge basalt (MORB) glass surrounded by powdered olivine in graphite–Pt double capsules at high pressure and powdered MORB in crucibles fabricated from single crystals of San Carlos olivine at one atmosphere. In these experiments, pressure and temperature were varied in such a way that we produced a series of liquids, each with an approximately constant composition (~12, ~15, and ~21 wt% MgO). Previously, we used a similar approach to show that \(D_{\text{Ni}}^{\text{ol/liq}}\) for a liquid with ~18 wt% MgO is a strong function of temperature. Combining the new data presented here with our previous results allows us to separate the effects of temperature from composition. We fit our data based on a Ni–Mg exchange reaction, which yields \(\ln \left( {D_{\text{Ni}}^{\text{molar}} } \right) = \frac{{ -\Delta _{r(1)} H_{{T_{\text{ref}} ,P_{\text{ref}} }}^{ \circ } }}{RT} + \frac{{\Delta _{r(1)} S_{{T_{\text{ref}} ,P_{\text{ref}} }}^{ \circ } }}{R} - \ln \left( {\frac{{X_{\text{MgO}}^{\text{liq}} }}{{X_{{{\text{MgSi}}_{ 0. 5} {\text{O}}_{ 2} }}^{\text{ol}} }}} \right).\) Each subset of constant composition experiments displays roughly the same temperature dependence of \(D_{\text{Ni}}^{\text{ol/liq}}\) (i.e.,\(-\Delta _{r(1)} H_{{T_{\text{ref}} ,P_{\text{ref}} }}^{ \circ } /R\)) as previously reported for liquids with ~18 wt% MgO. Fitting new data presented here (15 experiments) in conjunction with our 13 previously published experiments (those with ~18 wt% MgO in the silicate liquid) to the above expression gives \(-\Delta _{r(1)} H_{{T_{\text{ref}} ,P_{\text{ref}} }}^{ \circ } /R\) = 3641 ± 396 (K) and \(\Delta _{r(1)} S_{{T_{\text{ref}} ,P_{\text{ref}} }}^{ \circ } /R\) = ? 1.597 ± 0.229. Adding data from the literature yields \(-\Delta _{r(1)} H_{{T_{\text{ref}} ,P_{\text{ref}} }}^{ \circ } /R\) = 4505 ± 196 (K) and \(\Delta _{r(1)} S_{{T_{\text{ref}} ,P_{\text{ref}} }}^{ \circ } /R\) = ? 2.075 ± 0.120, a set of coefficients that leads to a predictive equation for \(D_{\text{Ni}}^{\text{ol/liq}}\) applicable to a wide range of melt compositions. We use the results of our work to model the melting of peridotite beneath lithosphere of varying thickness and show that: (1) a positive correlation between NiO in magnesian olivine phenocrysts and lithospheric thickness is expected given a temperature-dependent \(D_{\text{Ni}}^{\text{ol/liq}} ,\) and (2) the magnitude of the slope for natural samples is consistent with our experimentally determined temperature dependence. Alternative processes to generate the positive correlation between NiO in magnesian olivines and lithospheric thickness, such as the melting of olivine-free pyroxenite, are possible, but they are not required to explain the observed correlation of NiO concentration in initially crystallizing olivine with lithospheric thickness.  相似文献   

4.
This investigation is intended to evaluate the surface water quality of Brahmani River in order to determine its uses for different purposes. The water samples were collected from the strategic locations of the river from February 2014 to July 2015 and analyzed for physicochemical parameters such as water temperature; pH; electrical conductivity (EC); dissolved oxygen (DO); total dissolved solids (TDS); major cations, e.g., Na+, K+, Mg2+, Ca2+; and major anions, e.g., F?, Cl?, \( {\mathrm{SO}}_4^{2-} \), \( {\mathrm{NO}}_3^{-} \), \( {\mathrm{PO}}_4^{2-} \), and alkalinity. The water quality index (WQI) being a valuable and unique rating scale to depict the overall water quality status in a single term has been employed to determine the feasibility of using the river water as a source for various activities. The parameters with higher impact on water quality were selected to derive WQI of each selected sampling station. Results showed significant deterioration in quality of water at some of the sampling stations. WQI of Brahmani River ranged from 37.87 to 62.36 which falls in the range of good to poor quality of water. Pearson’s correlation matrix was derived to find possible interrelations among water quality parameters.  相似文献   

5.
Occurrences of arsenic (As) in the Bengal Basin of Bangladesh show close relationships with depositional environments and sediment textures. Hydrochemical data from three sites with varying physiography and sedimentation history show marked variations in redox status and dissolved As concentrations. Arsenic concentration in groundwater of the Ganges Flood Plain (GFP) is characteristically low, where high Mn concentrations indicate redox buffering by reduction of Mn(IV)-oxyhydroxides. Low DOC, \( {\text{HCO}}^{ - }_{3} \), \( {\text{NH}}^{ + }_{4} \) and high \( {\text{NO}}^{ - }_{3} \) and \( {\text{SO}}^{{2 - }}_{4} \) concentrations reflect an elevated redox status in GFP aquifers. In contrast, As concentration in the Ganges Delta Plain (GDP) is very high along with high Fe and low Mn. In the Meghna Flood Plain (MFP), moderate to high As and Fe concentrations and low Mn are detected. Degradation of organic matter probably drives redox reactions in the aquifers, particularly in MFP and GDP, thereby mobilising dissolved As. Speciation calculations indicate supersaturation with respect to siderite and vivianite in the groundwater samples at MFP and GDP, but groundwater in the GFP wells is generally supersaturated with respect to rhodochrosite. Values of log PCO2 at MFP and GDP sites are generally higher than at the GFP site. This is consistent with Mn(IV)-redox buffering suggested at the GFP site compared to Fe(III)-redox buffering at MFP and GDP sites.  相似文献   

6.
The nitrogen isotopic compositions of plant tissue could reflect its uptake of and preference for ammonium or nitrate. However, various factors may influence the field-collected δ15N values under field condition, which causes the interpretation problematic. The spatial variation of nitrogen (N) concentrations and the isotopic compositions were investigated in the soils and tissues of Chinese prickly ash from the southwest China to the east China. The objectives were to investigate the variation in soil and tissue δ15N values and N forms taken up by the plant. The leaf and root δ15N values varied significantly in response to the pattern of soil δ15N values. The difference in δ15N values between the leaves and roots was 2.57‰ and may be caused by an increase in the transport of unassimilated \( {\text{NO}}_{3}^{ - } \) and \( {\text{NH}}_{4}^{ + } \) to the leaves. Leaf nitrogen was significantly and positively correlated with leaf potassium and negatively related to leaf calcium. Because potassium is the favoured counter-cation for nitrate transport in the xylem, the enrichment of 15N in leaf relative to root induced by preferenced uptake of nitrate should be accompanied by significant and positive relationship of leaf nitrogen with leaf potassium concentrations. These results suggest that Chinese prickly ash prefers \( {\text{NO}}_{3}^{ - } \) over \( {\text{NH}}_{4}^{ + } \).  相似文献   

7.
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8.
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   

9.
The contamination levels of soils and water resources in Calabar, Nigeria have been investigated using resistivity (vertical electrical sounding and electrical resistivity tomography), geochemical analyses of soil and water resources and textural analysis. Sixty randomly sited VES sites were investigated in two seasons while ERT investigations were performed along four profiles. The geochemical investigations were spread across seasons in order to track seasonal changes in physico-chemical parameters: hydrogen ion concentration (pH), electrical conductivity, total dissolved solids, chloride ion (Cl?), nitrate ion (\( {\text{NO}}_{ 3}^{ - } \)), bicarbonate (\( {\text{HCO}}_{ 3}^{ - } \)), sulphate ion (\( {\text{SO}}_{ 4}^{2 - } \)), calcium ion (Ca2+), sodium ion (Na+), potassium ion (K+) and magnesium ion (Mg2+). Additionally, concentrations of ammonium, aluminium and nitrite ions in soils were determined. Results show that ionic concentrations in the sand-dominated soils and water are within permissible limits and baseline standards. The resistivities follow known trends in the area. However, at the central waste disposal site, a localised thin (< 5 m), low resistivity (< 15 Ωm) anomaly suspected to be due to contamination by leachates was observed. Comparatively, the contaminated area is also characterised by marginal increase in ionic concentrations. Strong attenuation capacities of overlying and adjoining clay/lateritic sediments and optimal design of the waste dump site probably reduced the spread of contaminants. The contaminated zone need to be closely monitored so that it does not extend to the aquifers. Hence, all strategies presently being used in managing wastes in Calabar should be sustained.  相似文献   

10.
Here we report new paleomagnetic results and precise paleopole position of the extensional study on \(\sim \)2367 Ma mafic giant radiating dyke swarm in the Dharwar craton, southern India. We have sampled 29 sites on 12 dykes from NE–SW Karimnagar–Hyderabad dykes and Dhone–Gooty sector dykes, eastern Dharwar craton to provide unambiguous paleomagnetism evidence on the spectacular radiating dyke swarm and thereby strengthening the presence of single magmatic event at \(\sim \)2367 Ma. A total of 158 samples were subjected to detailed alternating field and thermal demagnetization techniques and the results are presented here along with previously reported data on the same dyke swarm. The remanent magnetic directions are showing two components, viz., seven sites representing four dykes show component (A) with mean declination of \(94{{}^{\circ }}\) and mean inclination of \(-\,70{{}^{\circ }}\) (\(\hbox {k}=87\), \(\upalpha _{95}=10{{}^{\circ }}\)) and corresponding paleopole at \(16{{}^{\circ }}\hbox {N}\), \(41{{}^{\circ }}\hbox {E}\) (\(\hbox {dp}=15{{}^{\circ }}\) and \(\hbox {dm}=17{{}^{\circ }}\)) and 22 sites representing 8 dykes yielded a component (B) with mean declination of \(41{{}^{\circ }}\) and mean inclination of \(-\,21{{}^{\circ }}\) (\(\hbox {k}=41\), \(\upalpha _{95}=9{{}^{\circ }}\)) with a paleopole at \(41{{}^{\circ }}\hbox {N}\), \(200{{}^{\circ }}\hbox {E}\) (\(\hbox {dp}=5{{}^{\circ }}\) and \(\hbox {dm}=10{{}^{\circ }}\)). Component (A) results are similar to the previously reported directions from the \(\sim \)2367 Ma dyke swarm, which have been confirmed fairly reliably to be of primary origin. The component (B) directions appear to be strongly overprinted by the 2080 Ma event. The grand mean for the primary component (A) combined with earlier reported studies gives mean declination of \(97{{}^{\circ }}\) and mean inclination of \(-\,79{{}^{\circ }}\) (\(\hbox {k}=55\), \(\upalpha _{95}=3{{}^{\circ }}\)) with a paleopole at \(15{{}^{\circ }}\hbox {N}\), \(57{{}^{\circ }}\hbox {E}\) (\(\hbox {dp}=5{{}^{\circ }}\), \(\hbox {dm}=6{{}^{\circ }}\)). Paleogeographical position for the Dharwar craton at \(\sim \)2367 Ma suggests that there may be a chance to possible spatial link between Dharwar dykes of Dharwar craton (India), Widgemooltha and Erayinia dykes of Yilgarn craton (Australia), Sebanga Poort Dykes of Zimbabwe craton (Africa) and Karelian dykes of Kola-Karelia craton (Baltica Shield).  相似文献   

11.
Investigations were undertaken into the quality of surface water and groundwater bodies within the Upper Tigris Basin in Turkey to determine their suitability for potable and agricultural use. In the study area, the majority of the groundwater and surface water samples belong to the calcium–magnesium–bicarbonate type (Ca–Mg–HCO3) or magnesium–calcium–bicarbonate type (Mg–Ca–HCO3). Chemical analysis of all water samples shows that the mean cation concentrations (in mg/L) were in the order Ca2+ > Mg2+ > Na+ > K+ and that of anions are in the order \( \text{HCO}_{3}^{ - } \) > \( \text{SO}_{4}^{2 - } \) > Cl? > \( \text{CO}_{3}^{ - } \) for all groundwater and surface water samples. The Mg2+/Ca2+ ratio ranges from 0.21 to 1.30 with most of the values greater than 0.5, indicating that weathering of dolomites is dominant in groundwater. The analysis reveals that all of the samples are neutral to slightly alkaline (pH 7.0–8.7). Groundwater and surface water suitability for drinking usage was evaluated according to the World Health Organization and Turkish Standards (TSE-266) and suggests that most of the samples are suitable for drinking. Various determinants such as sodium absorption ratio, percent sodium (Na %), residual sodium carbonate and soluble sodium percentage revealed that most of the samples are suitable for irrigation. According to MH values, all of the well water samples were suitable for irrigation purposes, but 80 and 81.82% of Zillek springs and surface water samples were unsuitable. As per the PI values, the water samples from the study area are classified as Class I and Class II and are considered to be suitable for irrigation.  相似文献   

12.
The solubility of chromium in chlorite as a function of pressure, temperature, and bulk composition was investigated in the system Cr2O3–MgO–Al2O3–SiO2–H2O, and its effect on phase relations evaluated. Three different compositions with X Cr = Cr/(Cr + Al) = 0.075, 0.25, and 0.5 respectively, were investigated at 1.5–6.5 GPa, 650–900 °C. Cr-chlorite only occurs in the bulk composition with X Cr = 0.075; otherwise, spinel and garnet are the major aluminous phases. In the experiments, Cr-chlorite coexists with enstatite up to 3.5 GPa, 800–850 °C, and with forsterite, pyrope, and spinel at higher pressure. At P > 5 GPa other hydrates occur: a Cr-bearing phase-HAPY (Mg2.2Al1.5Cr0.1Si1.1O6(OH)2) is stable in assemblage with pyrope, forsterite, and spinel; Mg-sursassite coexists at 6.0 GPa, 650 °C with forsterite and spinel and a new Cr-bearing phase, named 11.5 Å phase (Mg:Al:Si = 6.3:1.2:2.4) after the first diffraction peak observed in high-resolution X-ray diffraction pattern. Cr affects the stability of chlorite by shifting its breakdown reactions toward higher temperature, but Cr solubility at high pressure is reduced compared with the solubility observed in low-pressure occurrences in hydrothermal environments. Chromium partitions generally according to \(X_{\text{Cr}}^{\text{spinel}}\) ? \(X_{\text{Cr}}^{\text{opx}}\) > \(X_{\text{Cr}}^{\text{chlorite}}\) ≥ \(X_{\text{Cr}}^{\text{HAPY}}\) > \(X_{\text{Cr}}^{\text{garnet}}\). At 5 GPa, 750 °C (bulk with X Cr = 0.075) equilibrium values are \(X_{\text{Cr}}^{\text{spinel}}\) = 0.27, \(X_{\text{Cr}}^{\text{chlorite}}\) = 0.08, \(X_{\text{Cr}}^{\text{garnet}}\) = 0.05; at 5.4 GPa, 720 °C \(X_{\text{Cr}}^{\text{spinel}}\) = 0.33, \(X_{\text{Cr}}^{\text{HAPY}}\) = 0.06, and \(X_{\text{Cr}}^{\text{garnet}}\) = 0.04; and at 3.5 GPa, 850 °C \(X_{\text{Cr}}^{\text{opx}}\) = 0.12 and \(X_{\text{Cr}}^{\text{chlorite}}\) = 0.07. Results on Cr–Al partitioning between spinel and garnet suggest that at low temperature the spinel- to garnet-peridotite transition has a negative slope of 0.5 GPa/100 °C. The formation of phase-HAPY, in assemblage with garnet and spinel, at pressures above chlorite breakdown, provides a viable mechanism to promote H2O transport in metasomatized ultramafic mélanges of subduction channels.  相似文献   

13.
Strain responses of frozen clay with thermal gradient under triaxial creep   总被引：1，自引：1，他引：0  
Thermal gradient is one of the main features for the temperature distribution in artificial frozen shaft lining (FSL). The time-dependent strain responses and the corresponding heterogeneity characteristics of frozen soils with thermal gradient are of potential significance for stability assessment and prediction of FSL, especially of the FSL embedded in thick alluvium. A series of triaxial creep tests were carried out on frozen saturated clay under various thermal gradients and creep stresses. The experimental results indicated that the triaxial creep curves for frozen clay with thermal gradient exhibit viscous characteristics, and the creep rate \(\Delta \varepsilon_{\text{a}} /\Delta t\) decreases with the increase in creep time \(t\) and decrease in thermal gradient. The stress–strain curve under different \(t\) showed that the creep stress has a marked growth when axial strain \(\varepsilon_{\text{a}} \le 1\,\%\). However, when \(\varepsilon_{\text{a}} \ge 1\,\%\), the growth rate decreases gradually. The deviation between measured radial strain \(\varepsilon_{\text{r}}^{\text{m}}\) under the middle specimen section height SSH and the calculated radial strain \(\varepsilon_{\text{r}}^{\text{c}}\) from the volumetric strain increases following a unified equation with the increase in axial strain. The radial strain \(\varepsilon_{\text{r}}^{\text{f}}\) for frozen clay with thermal gradient after experiment increases with the increase in SSH, and the slope of \( \varepsilon_{\text{r}}^{\text{f}} - {\text{SSH}} \) curve is significantly dependent on the thermal gradient and creep stress. The variation of \(\varepsilon_{\text{r}}^{\text{m}} - \varepsilon_{\text{r}}^{\text{c }}\) during experiment and \(\varepsilon_{\text{r}}^{\text{f}}\) distribution after experiment are the macro-responses of internal micro-heterogeneities in frozen soils induced from thermal gradient, and are closely related to strain rate and its variation. These observations and findings provide an insight into the creep mechanism and the estimation method of creep deformation for frozen soils with thermal gradient.  相似文献   

14.
Fluoride (F?) is the most important element for human health. Hydrogeochemical survey was conducted to probe into the controlling factors of F? in the groundwater of a semi-arid part of South India. The study area comprises of F?-bearing minerals (hornblende, biotite, and apatite) in the Precambrian rocks, sandstones in the Upper Gondwana rocks, and clays in the Quaternary formations. Forty-seven percent of the total groundwater samples have the higher F? content than its permissible limit of 1.50 mg/L prescribed for drinking purpose. The chemical data of the groundwater is analyzed to assess the geochemical processes dominating the F?-bearing groundwater, using Piper and Gibbs diagrams, correlations, saturation indices, ionic ratios, and multivariate analysis. Piper diagram shows that the groundwater quality is characterized by Na+-HCO\( {}_3^{-} \) and Na+-Cl?types, while the Gibbs diagrams suggest that the groundwater chemistry is mainly controlled by water-rock interactions and is subsequently modified by human activities. The F? groundwater is positively correlated with pH, total dissolved solids, Mg2+, Na+, K+, HCO\( {}_3^{-} \), Cl?, SO\( {}_4^{2-} \), and NO\( {}_3^{-} \) and negatively with Ca2+, representing the influences of geogenic and anthropogenic origins on the groundwater system. Geochemical ratios and saturation indices indicate that the processes of mineral dissolution, ion exchange, and evaporation mainly govern the high F? groundwater, while the chemical fertilizers cause for the enrichment of F?in the groundwater. Cluster and principal component analyses further support the above findings.  相似文献   

15.
Petrography and mineralogy of four calc-alkaline granitoid plutons Agarpur, Sindurpur, Raghunathpur and Sarpahari located from west to east of northern Purulia of Chhotanagpur Gneissic Complex, eastern India, are investigated. The plutons, as a whole, are composed of varying proportions of Qtz–Pl–Kfs–Bt–Hbl±Px–Ttn–Mag–Ap–Zrn±Ep. The composition of biotite is consistent with those of calc-alkaline granitoids. Hornblende–plagioclase thermometry, aluminium-in-hornblende barometry and the assemblage sphene–magnetite–quartz were used to determine the P, T and \(f_{\mathrm{O}_2}\) during the crystallisation of the parent magmas in different plutons. The plutons are crystallised under varying pressures (6.2–2.4 kbar) and a wide range of temperatures (896–\(718{^{\circ }}\hbox {C}\)) from highly oxidised magmas (log \(f_{\mathrm{O}_2}\) \(-11.2\) to \(-15.4\) bar). The water content of the magma of different plutons varied from 5.0 to 6.5 wt%, consistent with the calc-alkaline nature of the magma. Calc-alkaline nature, high oxygen fugacity and high \(\hbox {H}_{2}\hbox {O}_{{\mathrm{melt}}}\) suggest that these plutons were emplaced in subduction zone environment. The depths of emplacement of these plutons seem to increase from west to east. Petrologic compositions of these granitoids continuously change from enderbite (opx-tonalite: Sarpahari) in the east to monzogranite (Raghunathpur) to syenogranite (Sindurpur) to alkali feldspar granite (Agarpur) in the west. The water contents of the parental magmas of different plutons also increase systematically from east to west. No substantial increase in the depth of emplacement is found in these plutons lying south and north of the major shear zone passing through the study area suggesting the strike-slip nature of the east–west shear zone.  相似文献   

16.
This article formulates the experimentally substantiated physical principle that the natural stress condition of the Earth’s crust is formed due to the superposition of stress fields, which is caused by the gravitational forces of the Earth and by tectonic and astrophysical forces that are produced by physical processes in space. The natural stress field is represented by the stress tensor regulatory components: \(\sigma _{z}^{{\text{N}}}\) = \( - \gamma H + {{\sigma }_{{zT}}} + {{\sigma }_{{z{\text{AF}}}}}\), \(\sigma _{x}^{{\text{N}}}\) = \( - \lambda \gamma H + {{\sigma }_{{xT}}} + {{\sigma }_{{x{\text{AF}}}}}\), \(\sigma _{y}^{{\text{N}}}\) = \( - \lambda \gamma H + {{\sigma }_{{yT}}} + {{\sigma }_{{y{\text{AF}}}}}\).  相似文献   

17.
The pressure–volume–temperature (P–V–T) relation of CaIrO3 post-perovskite (ppv) was measured at pressures and temperatures up to 8.6 GPa and 1,273 K, respectively, with energy-dispersive synchrotron X-ray diffraction using a DIA-type, cubic-anvil apparatus (SAM85). Unit-cell dimensions were derived from the Le Bail full profile refinement technique, and the results were fitted using the third-order Birth-Murnaghan equation of state. The derived bulk modulus \( K_{T0} \) at ambient pressure and temperature is 168.3 ± 7.1 GPa with a pressure derivative \( K_{T0}^{\prime } \) = 5.4 ± 0.7. All of the high temperature data, combined with previous experimental data, are fitted using the high-temperature Birch-Murnaghan equation of state, the thermal pressure approach, and the Mie-Grüneisen-Debye formalism. The refined thermoelastic parameters for CaIrO3 ppv are: temperature derivative of bulk modulus \( (\partial K_{T} /\partial T)_{P} \) = ?0.038 ± 0.011 GPa K?1, \( \alpha K_{T} \) = 0.0039 ± 0.0001 GPa K?1, \( \left( {\partial K_{T} /\partial T} \right)_{V} \) = ?0.012 ± 0.002 GPa K?1, and \( \left( {\partial^{2} P/\partial T^{2} } \right)_{V} \) = 1.9 ± 0.3 × 10?6 GPa2 K?2. Using the Mie-Grüneisen-Debye formalism, we obtain Grüneisen parameter \( \gamma_{0} \) = 0.92 ± 0.01 and its volume dependence q = 3.4 ± 0.6. The systematic variation of bulk moduli for several oxide post-perovskites can be described approximately by the relationship K T0  = 5406.0/V(molar) + 5.9 GPa.  相似文献   

18.
Owing to the lack of consistent spatial time series data on actual evapotranspiration (ET), very few studies have been conducted on the long-term trend and variability in ET at a national scale over the Indian subcontinent. The present study uses biome specific ET data derived from NOAA satellite’s advanced very high resolution radiometer to investigate the trends and variability in ET over India from 1983 to 2006. Trend analysis using the non-parametric Mann–Kendall test showed that the domain average ET decreased during the period at a rate of \(0.22\,\hbox {mm year}^{-1}\). A strong decreasing trend (\(m = -1.75\, \hbox {mm year}^{-1}\), \(F = 17.41\), \(P\) 0.01) was observed in forest regions. Seasonal analyses indicated a decreasing trend during southwest summer monsoon (\(m= -0.320\, \hbox {mm season}^{-1}\,\hbox {year}^{-1})\) and post-monsoon period (\(m= -0.188\, \hbox {mm season}^{-1 }\,\hbox {year}^{-1})\). In contrast, an increasing trend was observed during northeast winter monsoon (\(m = 0.156 \,\hbox {mm season}^{-1 }\,\hbox {year}^{-1})\) and pre-monsoon (\(m = 0.068\, \hbox {mm season}^{-1 }\,\hbox {year}^{-1})\) periods. Despite an overall net decline in the country, a considerable increase ( \(4 \,\hbox {mm year}^{-1}\)) was observed over arid and semi-arid regions. Grid level correlation with various climatic parameters exhibited a strong positive correlation (\(r \!>\!0.5\)) of ET with soil moisture and precipitation over semi-arid and arid regions, whereas a negative correlation (\(r\) \(-0.5\)) occurred with temperature and insolation in dry regions of western India. The results of this analysis are useful for understanding regional ET dynamics and its relationship with various climatic parameters over India. Future studies on the effects of ET changes on the hydrological cycle, carbon cycle, and energy partitioning are needed to account for the feedbacks to the climate.  相似文献   

19.
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   

20.
The specific heat capacity (C p) of six variably hydrated (~3.5 wt% H2O) iron-bearing Etna trachybasaltic glasses and liquids has been measured using differential scanning calorimetry from room temperature across the glass transition region. These data are compared to heat capacity measurements on thirteen melt compositions in the iron-free anorthite (An)–diopside (Di) system over a similar range of H2O contents. These data extend considerably the published C p measurements for hydrous melts and glasses. The results for the Etna trachybasalts show nonlinear variations in, both, the heat capacity of the glass at the onset of the glass transition (i.e., C p g ) and the fully relaxed liquid (i.e., C p l ) with increasing H2O content. Similarly, the “configurational heat capacity” (i.e., C p c  = C p l  ? C p g ) varies nonlinearly with H2O content. The An–Di hydrous compositions investigated show similar trends, with C p values varying as a function of melt composition and H2O content. The results show that values in hydrous C p g , C p l and C p c in the depolymerized glasses and liquids are substantially different from those observed for more polymerized hydrous albitic, leucogranitic, trachytic and phonolitic multicomponent compositions previously investigated. Polymerized melts have lower C p l and C p c and higher C p g with respect to more depolymerized compositions. The covariation between C p values and the degree of polymerization in glasses and melts is well described in terms of SMhydrous and NBO/T hydrous. Values of C p c increase sharply with increasing depolymerization up to SMhydrous ~ 30–35 mol% (NBO/T hydrous ~ 0.5) and then stabilize to an almost constant value. The partial molar heat capacity of H2O for both glasses (\( C_{{{\text{p}}\;{\text{H}}_{2} {\text{O}}}}^{\text{g}} \)) and liquids (\( C_{{{\text{p}}\;{\text{H}}_{2} {\text{O}}}}^{\text{l}} \)) appears to be independent of composition and, assuming ideal mixing, we obtain a value for \( C_{{{\text{p}}\;{\text{H}}_{2} {\text{O}}}}^{\text{l}} \) of 79 J mol?1 K?1. However, we note that a range of values for \( C_{{{\text{p}}\;{\text{H}}_{2} {\text{O}}}}^{\text{l}} \) (i.e., ~78–87 J mol?1 K?1) proposed by previous workers will reproduce the extended data to within experimental uncertainty. Our analysis suggests that more data are required in order to ascribe a compositional dependence (i.e., nonideal mixing) to \( C_{{{\text{p}}\;{\text{H}}_{2} {\text{O}}}}^{\text{l}} \).  相似文献   

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