天星河、文峰河流域岩溶水化学及影响因素     

李明伦  焦杰松  张红波 《江苏地质》2015,39(1):99-104

重庆东北部地区巫溪天星河、文峰河的岩溶流域水化学特征研究结果表明:研究区泉水样品的p H值为6.47~8.28,平均值为7.79;流域河水饱和指数(SIc)的平均值为0.14,表明其变化受到流域碳酸盐岩分布的控制。水化学类型以HCO3-Ca型水为主,Ca2+和HCO-3平均分别占阳、阴离子的75%和82%。通过分析Gibbs图,发现泉水的主要组分属于"岩石风化类型",主要反映了岩石的溶解作用对泉水水化学的影响。流域内部分水样NO-3和SO2-4较高,可能是受工农业生产等人类活动的影响引起,此外硫酸也参与了碳酸盐矿物的溶解。  相似文献   

Accuracy and precision of different sampling strategies and flux integration methods for runoff water: comparisons based on measurements of the electrical conductivity     

Patrick Schleppi  Peter A. Waldner  Bruno Fritschi 《水文研究》2006,20(2):395-410

Because of their fast response to hydrological events, small catchments show strong quantitative and qualitative variations in their water runoff. Fluxes of solutes or suspended material can be estimated from water samples only if an appropriate sampling scheme is used. We used continuous in‐stream measurements of the electrical conductivity of the runoff in a small subalpine catchment (64 ha) in central Switzerland and in a very small (0·16 ha) subcatchment. Different sampling and flux integration methods were simulated for weekly water analyses. Fluxes calculated directly from grab samples are strongly biased towards high conductivities observed at low discharges. Several regressions and weighted averages have been proposed to correct for this bias. Their accuracy and precision are better, but none of these integration methods gives a consistently low bias and a low residual error. Different methods of peak sampling were also tested. Like regressions, they produce important residual errors and their bias is variable. This variability (both between methods and between catchments) does not allow one to tell a priori which sampling scheme and integration method would be more accurate. Only discharge‐proportional sampling methods were found to give essentially unbiased flux estimates. Programmed samplers with a fraction collector allow for a proportional pooling and are appropriate for short‐term studies. For long‐term monitoring or experiments, sampling at a frequency proportional to the discharge appears to be the best way to obtain accurate and precise flux estimates. Copyright © 2006 John Wiley & Sons, Ltd.  相似文献   

Response of surface water chemistry to reduced levels of acid precipitation: comparison of trends in two regions of New York,USA     

Douglas A. Burns  Michael R. McHale  Charles T. Driscoll  Karen M. Roy 《水文研究》2006,20(7):1611-1627

In light of recent reductions in sulphur (S) and nitrogen (N) emissions mandated by Title IV of the Clean Air Act Amendments of 1990, temporal trends and trend coherence in precipitation (1984–2001 and 1992–2001) and surface water chemistry (1992–2001) were determined in two of the most acid‐sensitive regions of North America, i.e. the Catskill and Adirondack Mountains of New York. Precipitation chemistry data from six sites located near these regions showed decreasing sulphate (SO₄^2?), nitrate (NO₃^?), and base cation (C_B) concentrations and increasing pH during 1984–2001, but few significant trends during 1992–2001. Data from five Catskill streams and 12 Adirondack lakes showed decreasing trends in SO₄^2? concentrations at all sites, and decreasing trends in NO₃^?, C_B, and H⁺ concentrations and increasing trends in dissolved organic carbon at most sites. In contrast, acid‐neutralizing capacity (ANC) increased significantly at only about half the Adirondack lakes and in one of the Catskill streams. Flow correction prior to trend analysis did not change any trend directions and had little effect on SO₄^2? trends, but it caused several significant non‐flow‐corrected trends in NO₃^? and ANC to become non‐significant, suggesting that trend results for flow‐sensitive constituents are affected by flow‐related climate variation. SO₄^2? concentrations showed high temporal coherence in precipitation, surface waters, and in precipitation–surface water comparisons, reflecting a strong link between S emissions, precipitation SO₄^2? concentrations, and the processes that affect S cycling within these regions. NO₃^? and H⁺ concentrations and ANC generally showed weak coherence, especially in surface waters and in precipitation–surface water comparisons, indicating that variation in local‐scale processes driven by factors such as climate are affecting trends in acid–base chemistry in these two regions. Copyright © 2005 John Wiley & Sons, Ltd.  相似文献   

Distribution of hydrate on Europa: Further evidence for sulfuric acid hydrate     

R.W. Carlson  M.S. Anderson  R.E. Johnson 《Icarus》2005,177(2):461-471

Sulfuric acid hydrate has been proposed as an important species on Europa's surface, the acid being produced by radiolysis of surficial sulfur compounds. We investigated the spectral properties of disordered and crystalline forms of sulfuric acid and suggest that the hydration properties of Europa's hypothesized sulfuric acid lie between two end members: liquid sulfuric acid and its higher crystalline hydrates. The spectra of these end members are similar except for spectral shifts at the band edges. We measured the optical constants of sulfuric acid octahydrate and used these with simple radiative transfer calculations to fit Europa spectra obtained by Galileo's Near Infrared Mapping Spectrometer (NIMS). The global distribution of the hydrate that we associate here with hydrated sulfuric acid shows a strong trailing-side enhancement with a maximum fractional hydrate abundance of 90% by volume, corresponding to a sulfur atom to water molecule ratio of 10%. The hydrate concentration spatially correlates with the ultraviolet and visible absorption of the surface and with the sulfur dioxide concentration. The asymmetric global distribution is consistent with Iogenic plasma ion implantation as the source of the sulfur, possibly modified by electron irradiation and sputtering effects. The variegated distribution also correlates with geologic forms. A high spatial resolution image shows resolved lineae with less hydrate appearing within the lineae than in nearby crustal material. The low concentration of hydrated material in these lineae argues against their conveying sulfurous material to the surface from the putative ocean.  相似文献   

Elastic collisions in ion irradiation experiments: A mechanism for space weathering of silicates   总被引：1，自引：0，他引：1  

Rosario Brunetto  Giovanni Strazzulla 《Icarus》2005,179(1):265-273

Ion irradiation experiments have been performed on silicates (bulk samples) rich of olivine, pyroxene, and serpentine to simulate the effects of space weathering induced on asteroids by solar wind ions. We have used different ions (H⁺, He⁺, Ar⁺, Ar²⁺) having different energies (from 60 to 400 keV) to weather the samples, probed by Raman spectroscopy and UV-vis-NIR reflectance spectroscopy. All the irradiated materials have shown reddening and darkening of reflectance spectra in the 0.25-2.7 μm spectral range. We have found that the increase of the spectral slope of the continuum across the 1-μm band is strongly related with the number of displacements caused by colliding ions because of elastic collisions with the target nuclei. The spectral slopes have been compared, at increasing ion fluence, with those from irradiated Epinal meteorite. We show that formation of nuclear displacements by solar wind ion irradiation is a physical mechanism that reddens the asteroidal surfaces on a time-scale lower than 10⁶ years.  相似文献   

Effects of catastrophic flooding on stream biogeochemistry in a headwater stream in Shenandoah National Park,USA     

K.S. Reinhardt  T. Furman 《水文研究》2008,22(18):3759-3771

This study examined the stream chemistry changes in Staunton River (a second‐order headwater stream with an average annual discharge 704 m³ ha^?1 yr^?1, Shenandoah National Park, Virginia) resulting from a catastrophic flood in June 1995. This flood, which followed after 800 mm of rain in a 4‐day period, caused large‐scale debris flows and complete scouring of riparian soils down to bedrock in the lower 2 km of the stream, and has been estimated to be a 1000‐year flood. The flood affected stream chemistry on both short‐ and long‐term time scales. The primary short‐term response was elevations in stream concentration of Ca²⁺, Mg²⁺, and K⁺ by 59%, 87%, and 49%, respectively, for 6 months immediately following the flood. The long‐term impact of decreased concentration of all base cations and SiO₂ during summer months (8% average) lasted about 2 years. At the episodic time scale, Ca²⁺, Mg²⁺, and K⁺ flushed from soil sources during pre‐flood storms while Na⁺ and SiO₂ diluted; these trends generally reversed during post‐flood storms for 2 years. Short‐term effects are attributed to the leaching of unconsolidated soil and upturned organic matter that clogged the streambed after the flood. The long‐term and superimposed episodic impacts may have resulted from the loss of riparian soils and vegetation in the flood. Copyright © 2008 John Wiley & Sons, Ltd.  相似文献   

Chronological Study of Coal-seam Water and its Implication on Gas Production in the South Qinshui Basin     

CHEN Biying  FANG Luji  LANG Yunchao  XU Sheng  LIU Congqiang  ZHANG Luyuan  HOU Xiaolin 《《地质学报》英文版》2024,98(1):207-219

The knowledge of the residence time of formation water is fundamental to understanding the subsurface flow and hydrological setting. To better identify the origin and evolution of coal seam water and its impact on gas storage and production, this study collected coalbed methane co-produced water in the southeast Qinshui Basin and detected chemical and isotopic compositions, especially 36Cl and 129I concentrations. The calculated tracer ages of 129I (5.2–50.6 Ma) and 36Cl (0.13–0.76 Ma) are significantly younger than the age of coal-bearing formation (Pennsylvanian - Cisuralian), indicating freshwater recharge after coal deposition. The model that utilises 129I/I and 36Cl/Cl ratios to constrain the timing of recharge and the proportion of recharge water reveals that over 60% of pre-anthropogenic meteoric water entered coal seams since 10 Ma and mixed with residue initial deposition water, corresponding to the basin inversion in Cenozoic. The spatial distribution of major ion concentrations reveals the primary recharge pathway for meteoric water from coal outcrops at the eastern margin to the basin center. This study demonstrates the occurrence of higher gas production rates from wells that accept water recharge in recent times and suggests the possible potential of the non-stagnant zones for high gas production.  相似文献   

Petrographic, Chemical and B-Isotopic Insights into the Origin of Tourmaline-Rich Rocks and Boron Recycling in the Martinamor Antiform (Central Iberian Zone, Salamanca, Spain)   总被引：2，自引：0，他引：2  

PESQUERA  A.; TORRES-RUIZ  J.; GIL-CRESPO  P. P.; JIANG  S.-Y. 《Journal of Petrology》2005,46(5):1013-1044

Tourmaline in the Martinamor antiform occurs in tourmalinites(rocks with >15–20% tourmaline by volume), clasticmetasedimentary rocks of the Upper Proterozoic Monterrubio formation,quartz veins, pre-Variscan orthogneisses and Variscan graniticrocks. Petrographic observations, back-scattered electron (BSE)images, and microprobe data document a multistaged developmentof tourmaline. Overall, variations in the Mg/(Mg + Fe) ratiosdecrease from tourmalinites (0·36–0·75),through veins (0·38–0·66) to granitic rocks(0·23–0·46), whereas Al increases in thesame order from 5·84–6·65 to 6·22–6·88apfu. The incorporation of Al into tourmaline is consistentwith combinations of ^xAl(NaR)_–1 and AlO(R(OH))_–1exchange vectors, where ^x represents X-site vacancy and R is(Mg + Fe²⁺ + Mn). Variations in ^x/(^x + Na) ratios are similarin all the types of tourmaline occurrences, from 0·10to 0·53, with low Ca-contents (mostly <0·10apfu). Based on field and textural criteria, two groups of tourmaline-richrocks are distinguished: (1) pre-Variscan tourmalinites (probablyCadomian), affected by both deformation and regional metamorphismduring the Variscan orogeny; (2) tourmalinites related to thesynkinematic granitic complex of Martinamor. Textural and geochemicaldata are consistent with a psammopelitic parentage for the protolithof the tourmalinites. Boron isotope analyses of tourmaline havea total range of ¹¹B values from –15·6 to 6·8;the lowest corresponding to granitic tourmalines (–15·6to –11·7) and the highest to veins (1·9to 6·8). Tourmalines from tourmalinites have intermediate¹¹B values of –8·0 to +2·0. The observedvariations in ¹¹B support an important crustal recycling ofboron in the Martinamor area, in which pre-Variscan tourmaliniteswere remobilized by a combination of mechanical and chemicalprocesses during Variscan deformation, metamorphism and anatexis,leading to the formation of multiple tourmaline-bearing veinsand a new stage of boron metasomatism. KEY WORDS: tourmalinites; metamorphic and granitic rocks; mineral chemistry; whole-rock chemistry; boron isotopes  相似文献   

Volatile Organic Compounds in the Po Basin. Part B: Biogenic VOCs     

M.?Steinbacher  J.?Dommen  C.?Ordonez  S.?Reimann  F.?C.?Grüebler  J.?Staehelin  S.?Andreani-Aksoyoglu  A.?S.?H.?PrevotEmail author 《Journal of Atmospheric Chemistry》2005,51(3):293-315

Measurements of volatile organic compounds (VOCs) were performed in the Po Basin, northern Italy in early summer 1998, summer 2002, and autumn 2003. During the three campaigns, trace gases and meteorological parameters were measured at a semi-rural station, around 35 km north of the city center of Milan. Bimodal diurnal cycles of isoprene with highest concentrations in the morning and evening were found and could be explained by the interaction of emissions, chemical reactions, and vertical mixing. The diurnal cycle could be qualitatively reproduced by a three-dimensional Eulerian model. The nighttime decay of isoprene could be attributed mostly to reactions with NO₃, while the decay of the isoprene oxidation products could not be explained with the considered chemical reactions. Methanol reached very high mixing ratios, up to 150 ppb. High concentrations with considerable variability occurred during nights with high relative humidities and low wind speeds. The origin of these nighttime methanol concentrations is most likely local and biogenic but the specific source could not be identified.  相似文献   

Refined relationship between the position of the fundamental OH stretching and the first overtones for clays     

S.?PetitEmail author  A.?Decarreau  F.?Martin  R.?Buchet 《Physics and Chemistry of Minerals》2004,31(9):585-592

The aim of this paper is to determine a relationship between the wavenumbers of the first OH-stretching overtones (W_2OH) and the wavenumbers of the OH-stretching fundamentals (W_OH) to help to interpret the near-infrared (NIR) spectra. The first overtone (2OH) bands appear at wavenumbers less than twice those of the fundamental bands (OH), due to the anharmonic character of vibrations, X = W_2OH/2 - W_OH, with X being the anharmonicity constant. Talc samples with various crystal chemistries are used to solve the equation and the experimental data are well fitted with X = –85.6 cm^–1. As far as the authors are aware, it is the first time that the anharmonicity constant for the OH-stretching vibrations is determined for phyllosilicates. The anharmonicity constant remains almost unchanged for several types of clay samples. Therefore the relation, established from talc samples because their absorption bands are narrow and their wavenumber range of OH vibrations is wide, can be used for any other clay minerals.  相似文献