成都洛带上沙溪庙组气藏地层水分布特征研究

成都洛带沙溪庙组气藏普遍含水,气藏不同位置地层水含量对于天然气的产量及产出时间有很大的影响。地层水矿化度较高,属CaCl2型,具混合水的水化学特征。地层水与天然气共同赋存同一储层中,属于同一压力系统,与天然气伴生产出,无边、底水存在,缺乏有效补给。含水层往往分布于有利的沉积微相一分流河道及河口坝中,厚度大、物性好的砂体含水特征更为明显。通过对该气藏水水化学特征及气水关系的研究,初步明确了该地层水的分布特征。     

Estimating groundwater evapotranspiration rates using diurnal water-table fluctuations in a semi-arid riparian zone

In semi-arid climates, phreatophytes draw on shallow aquifers, and groundwater evapotranspiration (ET_G) is a principal component of groundwater budgets. Diurnal water table fluctuations, which often are a product of ET_G, were monitored in the riparian zone of Red Canyon Creek, Wyoming, USA. These fluctuations were higher in a riparian wetland (2–36 mm) than a grass-covered meadow (1–6 mm). The onset and cessation of water-table fluctuations correspond to daily temperatures relative to freezing. Spatial differences were due to vegetation type and specific yield, while temporal changes were due to vegetation dormancy. Ratios of ET_G to potential evapotranspiration (PET), K _c,GW, were similar to ratios of actual evapotranspiration (ET) to PET, K _c, in semi-arid rangelands. Before vegetation senescence, K _c,GW increased between precipitation events, suggesting phreatophytes pull more water from the saturated zone as soil moisture decreases. In contrast, K _c decreases with soil moisture following precipitation events as ET becomes increasingly water-limited. Error in ET_G is primarily from estimates of specific yield (S _y), which is difficult to quantify in heterogeneous sediments. ET_G values may be more reliable because the range of acceptable S _y is smaller than K _c and S _y does not change with vegetation type or soil moisture.     

Water balance in the playa-lakes of an arid environment,Monegros, NE Spain

The playa-lakes of the Monegros desert in north-east Spain are saline wetlands in an arid environment, a rare phenomenon in Europe. These extremely valuable habitats are threatened by changes associated with agricultural expansion and incorporation of new irrigated areas. An understanding of the present hydrologic regime will enable changes to be identified, particularly those brought about by flooding and pollution caused by irrigation surplus. This study sets out to show the results of applying a daily water balance in three selected playa-lakes. The balance was in two parts and consisted of: (1) the average balance for all the endorheic basin using the BALAN_11 program, and (2) the water balance in some playa-lakes, applying discharge flows obtained from the previous balance. The resulting volumes of water were converted to water depths and contrasted with reference volumes taken from field and Landsat images. The model was calibrated by applying various hypotheses of function which enabled the results to be adjusted. The proposed balance is an acceptable reproduction of field water measurements during this period, and underlines the consistency of the conceptual model. The methodology used is appropriate for understanding the playa-lakes function and for monitoring them for conservation purposes.     

Evaluation of distributed recharge in an upland semi-arid karst system: the West Bank Mountain Aquifer,Middle East

Assessment of recharge in a structurally complex upland karst limestone aquifer situated in a semi-arid environment is difficult. Resort to surrogate indicators such as measurement of spring outflow and borehole discharge, is a common alternative, and attempts to apply conventional soil moisture deficit analysis may not adequately account for the intermittent spate conditions that arise in such environments. A modelling approach has been made using the West Bank Mountain Aquifer system in the Middle East as a trial. The model uses object oriented software which allows various objects to be switched on and off. Each of the main recharge processes identified in the West Bank is incorporated. The model allows either conventional soil moisture deficit analysis calculations or wetting threshold calculations to be made as appropriate, and accommodates both direct recharge and secondary recharge. Daily time steps enable recharge and runoff routing to be calculated for each node. Model runs have enabled a series of simulations for each of the three aquifer basins in the West Bank and for the whole of the West Bank. These provide recharge estimates comparable to those prepared by earlier workers by conventional means. The model is adaptable and has been successfully used in other environments.     

A continuous/discontinuous Galerkin framework for modeling coupled subsurface and surface water flow

We consider conjunctive surface-subsurface flow modeling, where surface water flow is described by the shallow water equations and ground water flow by Richards’ equation for the vadose zone. Coupling between the models is based on the continuity of flux and water pressure. Numerical approximation of the coupled model using the framework of discontinuous Galerkin (DG) methods is formulated. In the subsurface, the local discontinuous Galerkin (LDG) method is used to approximate ground water velocity and hydraulic head; a DG method is also used to approximate surface water velocity and elevation. This approach allows for a weak coupling of the models and the use of different approximating spaces and/or meshes within each regime. A simplified LDG method based on continuous approximations to water head is also described. Numerical results that investigate physical and numerical aspects of surface–subsurface flow modeling are presented. This work was supported by National Science Foundation grant DMS-0411413.     

Groundwater resources in the Jabal Al Hass region,northwest Syria: an assessment of past use and future potential

In many cases, the development of groundwater resources to boost agricultural production in dry areas has led to a continuous decline in groundwater levels; this has called into question the sustainability of such exploitation. In developing countries, limited budgets and scarce hydrological data often do not allow groundwater resources to be assessed through groundwater modeling. A case study is presented of a low-cost water-balance approach to groundwater resource assessments in a 1,550 km² semi-arid region in northwestern Syria. The past development of irrigated agriculture and its effect on the groundwater system were studied by analysis of Landsat images and long-term groundwater level changes, respectively. All components of the groundwater balance were determined. Groundwater recharge was estimated using the chloride mass balance method. Over the past three decades, groundwater levels have declined, on average, 23 m, coinciding with a two-fold increase in the groundwater-irrigated area. Groundwater resources are currently depleted by a value that lies between 9.5×10⁶ and 118×10⁶ m³ year^?1, which is larger than can be compensated for by a future decrease in natural discharge or changes in boundary conditions. However, groundwater resources are likely to be sufficient to supply domestic and livestock needs in the area.     

Zircon M257 ‐ a Homogeneous Natural Reference Material for the Ion Microprobe U‐Pb Analysis of Zircon

We introduce and propose zircon M257 as a future reference material for the determination of zircon U‐Pb ages by means of secondary ion mass spectrometry. This light brownish, flawless, cut gemstone specimen from Sri Lanka weighed 5.14 g (25.7 carats). Zircon M257 has TIMS‐determined, mean isotopic ratios (2s uncertainties) of 0.09100 ± 0.00003 for ²⁰⁶pb/²³⁸U and 0.7392 ± 0.0003 for ²⁰⁷pb/²³⁵U. Its ²⁰⁶pb/²³⁸U age is 561.3 ± 0.3 Ma (unweighted mean, uncertainty quoted at the 95% confidence level); the U‐Pb system is concordant within uncertainty of decay constants. Zircon M257 contains ～ 840 μg g^?1 U (Th/U ～ 0.27). The material exhibits remarkably low heterogeneity, with a virtual absence of any internal textures even in cathodoluminescence images. The uniform, moderate degree of radiation damage (estimated from the expansion of unit‐cell parameters, broadening of Raman spectral parameters and density) corresponds well, within the “Sri Lankan trends”, with actinide concentrations, U‐Pb age, and the calculated alpha fluence of 1.66 × 10¹⁸ g^?1. This, and a (U+Th)/He age of 419 ± 9 Ma (2s), enables us to exclude any unusual thermal history or heat treatment, which could potentially have affected the retention of radiogenic Pb. The oxygen isotope ratio of this zircon is 13.9%o VSMOW suggesting a metamorphic genesis in a marble or calc‐silicate skarn.     

Composition-Induced Variations in SIMS Instrumental Mass Fractionation during Boron Isotope Ratio Measurements of Silicate Glasses

An analytical artefact is reported here related to differences in instrumental mass fractionation between NIST SRM glasses and natural geological glasses during SIMS boron isotope determinations. The data presented demonstrated an average 3.4‰ difference between the NIST glasses and natural basaltic to rhyolitic glasses mainly in terms of their sputtering-induced fractionation of boron isotopes. As no matrix effect was found among basaltic to rhyolitic glasses, instrumental mass fractionation of most natural glass samples can be corrected by using appropriate glass reference materials. In order to confirm the existence of the compositionally induced variations in boron SIMS instrumental mass bias, the observed offset in SIMS instrumental mass bias has been independently reproduced in two laboratories and the phenomenon has been found to be stable over a period of more than one year. This study highlights the need for a close match between the chemical composition of the reference material and the samples being investigated.     

Recommended Values of 239Pu, 240Pu and 239+240Pu Concentrations in Reference Material IAEA-315 (Marine Sediment) Estimated by Thermal Ionisation Mass Spectrometry, Inductively Coupled Plasma-Mass Spectrometry and Alpha Spectrometry

The recommended concentrations of ²³⁹Pu, ²⁴⁰Pu and ^239+240Pu in reference material IAEA‐315 (marine sediment) were estimated by three analytical methods: isotope dilution thermal ionisation mass spectrometry (TIMS), isotope dilution inductively coupled plasma‐mass spectrometry (ICP‐MS) and alpha spectrometry. The determination of ²³⁹Pu and ²⁴⁰Pu (^239+240Pu by alpha spectrometry) was carried out with samples from randomly selected bottles using each method. Plutonium‐238 was also measured by alpha spectrometry. A plutonium‐242 reference material was used as a spike for the quantitative analysis. The influence of ²⁴²Pu in the samples was therefore calculated; however, this contribution was less than the range of uncertainty and did not influence the final results. The obtained data were statistically analysed using variance component analysis and paired comparison. The combined standard uncertainties from “method/measurement”, “bottle” and “sub‐sample” were in the order of 3 to 6%. The main contributions to the uncertainty were from the material heterogeneity and from systematic differences between methods. Based on this study with twenty‐seven analyses using 10–14 g sample mass, concentrations of (38 ± 3) Bq kg^?1, (28 ± 3) Bq kg^?1 and (66 ± 4) Bq kg^?1 are proposed as recommended values for ²³⁹Pu, ²⁴⁰Pu and ^239+240Pu, respectively, and (9.5 ± 0.4) Bq kg^?1 for ²³⁸Pu as an information value in reference material IAEA‐315. In mass concentration units, these amount to (16.4 ± 1.2) ng kg^?1, (3.3 ± 0.4) ng kg^?1 and (0.015 ± 0.003) ng kg^?1 for ²³⁹Pu, ²⁴⁰Pu and ²³⁸Pu, respectively. The certified reference materials NIST 4350B and NIST 4354 were also analysed by TIMS for quality assurance of the method used in this study.     

A spectrophotometric measurement of soil cation exchange capacity based on cobaltihexamine chloride absorbance

Among numerous methods for cation exchange capacity (CEC) determination for soils and sediments, the cobaltihexamine chloride method is frequently used due to its ability to measure CEC at soil pH. After exchange with Co(NH₃)₆³⁺ ions, CEC is estimated via the measurement of the Co remaining in solution. The modified method proposed allows a more rapid determination of CEC based on the measurement of the absorbance at 472 nm of the cobaltihexamine chloride solution before and after exchange. This method has been applied to various soil's horizons from four sites, selected to cover a wide range of CEC and pH values. The model obtained allows one to calculate CEC from absorbance at 472 nm with 95% confidence intervals. As CEC is of relevant meaning in agronomical and environmental purposes, and more recently in ecotoxicological studies, this modified method can be proposed as a rapid test for CEC evaluation.