Influence of ignimbrite on the chemistry of river water in Shirasu plateau,Japan

River, rain and spring water samples from a region covered in “Shirasu” ignimbrite were collected on Kyushu Island, Japan. The analytical results were subjected to multivariate statistical analysis and stoichiometric calculation to understand the geographical distribution of chemical components in water and to extract geochemical underlying factors. The multivariate statistical analysis showed that the river-water chemistry is only slightly influenced by hot springs or polluted waters, but is highly controlled by weathering of ignimbrite. On the basis of the stoichiometric calculation based on water–rock interaction, the water chemistry was successfully estimated by a simple equation:\({\left[ {{\text{Si}}} \right]}{\text{ = 2}}{\left[ {{\text{Na}}^{{\text{ + }}} } \right]}{\text{ + }}{\left[ {{\text{Mg}}^{{{\text{2 + }}}} } \right]}\) in the upstream area, complemented by \({\left[ {{\text{Si}}} \right]}{\text{ = }}{\left[ {{\text{Na}}^{{\text{ + }}} } \right]}{\text{ - 3}}{\left[ {{\text{K}}^{{\text{ + }}} } \right]}{\text{ + }}{\left[ {{\text{Mg}}^{{{\text{2 + }}}} } \right]}{\text{ - 2}}{\left[ {{\text{Ca}}^{{{\text{2 + }}}} } \right]}\) in the downstream area.     

Seasonal patterns of carbon chemistry and isotopes in tufa depositing groundwaters of southwestern Japan

Annually laminated carbonates, known as tufas, commonly develop in limestone areas and typically record seasonal patterns of oxygen- and carbon-isotope compositions. δ¹⁸O values are principally controlled by seasonal changes of water temperature, whereas δ¹³C values are the result of complex reactions among the gaseous, liquid, and solid sources of carbon in the system. We examined the processes that cause the seasonal patterns of δ¹³C in groundwater systems at three tufa-depositing sites in southwestern Japan by applying model calculations to geochemical data. Underground inorganic carbon species are exchanged with gaseous CO₂, which is mainly introduced to the underground hydrological system by natural atmospheric ventilation and by diffusion of soil air. These processes control the seasonal pattern of δ¹³C, which is low in summer and high in winter. Among the three sites we investigated, we identified two extreme cases of the degree of carbon exchange between liquid and gaseous phases. For the case with high radiocarbon composition (Δ¹⁴C) and low pCO₂, there was substantial carbon exchange because of a large contribution of atmospheric CO₂ and a small water mass. For the other extreme case, which was characterized by low Δ¹⁴C and high pCO₂, the contribution of atmospheric CO₂ was small and the water mass was relatively large. Our results suggest that at two of the three sites water residence time within the soil profile was longer than 1 year. Our results also suggested a short residence time (less than 1 year) of water in the soil profile at the site with the smallest water mass, which is consistent with large seasonal amplitude of the springwater temperature variations. The Δ¹⁴C value of tufas is closely related to the hydrological conditions in which they are deposited. If the initial Δ¹⁴C value of a tufa-depositing system is stable, ¹⁴C-chronology can be used to date paleo-tufas.     

Borehole water and hydrologic model around the Nojima fault, SW Japan

The active fault drilling at Nojima Hirabayashi after the 1995 Hyogoken-nanbu (Kobe) earthquake (M_JMA = 7.2) provides us with a unique opportunity to investigate subsurface fault structure and the in-situ properties of fault and fluid. The borehole intersected the fault gouge of the Nojima fault at a depth interval of 623 m to 625 m. The lithology is mostly Cretaceous granodiorite with some porphyry dikes.The fault core is highly permeable due to fracturing. The borehole water was sampled in 1996 and 2000 from the depth interval between 630 and 650 m, just below the fault core. The chemical and isotopic compositions were analyzed. Carbon and oxygen isotope ratios of carbonates from the fault core were analyzed to estimate the origin of fluid.The following conclusions were obtained. (1) The ionic and isotopic compositions of borehole water did not change from 1996 to 2000. They are mostly derived from local ground water as mentioned by Sato and Takahashi [Sato, T., Takahashi, M., 2000. Chemical and isotopic compositions of groundwater obtained from the Hirabayashi well. Geological Survey of Japan Interim Report No. EQ/00/1, 187–192.]. (2) Geochemical speciation revealed that the borehole water was derived from a relatively deep reservoir, which may be situated at a depth of 3 to 4 km where the temperature is about 80–90 °C. (3) The shallower part of the Nojima fault (shallower than the reservoir depth) has not been healed from the hydrological viewpoints 5 years after the event, in contrast to the rapid healing detected by S wave splitting [Tadokoro, K., Ando, M., 2002. Evidence for rapid fault healing derived from temporal changes in S wave splitting, Geophys. Res. Lett., 29, 10.1029/2001GL013644.]. (4) Precipitation of calcite from the present borehole water since drilling supports the idea of precipitation of some calcite in coseismic hydraulic fractures in the fault core [Boullier, A-M., Fujimoto, K., Ohtani, T., Roman-Ross, G., Lewin, E., Ito, H., Pezard, P., Ildefonse, B., 2004. Textural evidence for recent co-seismic circulation of fluids in the Nojima fault zone, Awaji Island, Japan., Tectonophysics, 378, 165–181.]. (5) Carbon and oxygen isotope ratios of calcite indicated that the meteoric water flux had been localized at the fault core. (6) A difference in the carbon isotope ratio between the footwall and the hanging wall suggests that the fault has been acted as a hydrologic barrier, although the permeability along the fault is still high.     

Impact of natural water chemistry on public drinking water in Japan

Drinking water from Japan (Toyama, Kumamoto, Osaka, and Tokyo Prefecture) and France (Volvic water) was evaluated for taste and health properties using an index based on major and trace mineral content and organoleptic components. Although various reports point to calcium (Ca²⁺) as a key ingredient imparting good taste and magnesium (Mg²⁺) and sulfate (SO₄ ^2?) as causing unpleasant taste in drinking water, recent sensory threshold experiments have indicated that other major ions and minerals directly or indirectly contribute to good taste, including potassium (K), silica (SiO₂), and phosphorous (P). The present study examined major and trace constituents in water to accurately quantify water taste, flavor, and health effects in good-tasting (Volvic, Toyama, and Kumamoto water) and average-tasting water (Osaka and Tokyo water). Trace metal, volatile organic carbon, non-purgeable organic carbon and total inorganic carbon levels were evaluated as parameters influencing the sensory properties of the drinking water. All of the representative good-tasting water contained higher amounts of tasty minerals (Ca²⁺, K⁺, SiO₂) and lower amounts of unsavory, rough (Mg²⁺ and SO₄ ^2?), and bitter (Cl^?) minerals. Stiff diagrams of the water samples indicated that good-tasting water was generally bicarbonate (HCO₃ ^?) type. Seasonal variations in physicochemical parameters did not change the order of abundance of cations and anions but did affect the concentration of various ions present in the water. Trace metals also affected water flavor. Mn facilitates acetaldehyde formation and Fe is associated with polyphenolic oxidation and formation of organoleptic flavor constituents. Trihalomethanes (THMs) may also cause unpleasant drinking water flavors or odors. THMs concentrations for all samples were below 5.7 μg/L, meeting the safety and taste requirements for good drinking water. The Japanese samples were compared against Volvic water, which was used as a standard for good-tasting water. Total dissolved solids concentrations were below 300 mg/L for all specimens, in compliance with World Health Organization guidelines. The results are discussed on the basis of the balance between inorganic major ions and trace minerals and THMs concentration thresholds.     

Surface water chemistry and nitrate pollution in Shimabara,Nagasaki, Japan

Groundwater is a finite resource that is threatened by pollution all over the world. Shimabara City, Nagasaki, Japan, uses groundwater for its main water supply. During recent years, the city has experienced severe nitrate pollution in its groundwater. For better understanding of origin and impact of the pollution, chemical effects and surface–groundwater interactions need to be examined. For this purpose, we developed a methodology that builds on joint geochemical analyses and advanced statistical treatment. Water samples were collected at 42 sampling points in Shimabara including a part of Unzen City. Spatial distribution of water chemistry constituents was assessed by describing Stiff and Piper diagrams using major ions concentrations. The nitrate (NO₃?+?NO₂–N) concentration in 45% of water samples exceeded permissible Japanese drinking level of 10 mg L^??1. Most of the samples showed Ca–HCO₃ or Ca–(NO₃?+?SO₄) water types. Some samples were classified into characteristic water types such as Na–Cl, (Na?+?K)–HCO₃, (Na?+?K)–(SO₄?+?NO₃), and Ca–Cl. Thus, results indicated salt water intrusion from the sea and anthropogenic pollution. At the upstream of Nishi River, although water chemistry was characterized as Ca–HCO₃, ion concentrations were higher than those of other rivers. This is probably an effect of disinfection in livestock farming using slaked lime. Positive correlation between NO₃^? and SO₄^2?, Mg²⁺, Ca²⁺, Na⁺, K⁺, and Cl^? (r?=?0.32–0.64) is evidence that nitrate pollution sources are chemical fertilizers and livestock waste. Principal component analysis showed that chemistry of water samples can be explained by three main components (PCs). PC1 depicts general ion concentration. PC2 and PC3 share influence from chemical fertilizer and livestock waste. Cluster analyses grouped water samples into four main clusters. One of these is the general river chemistry mainly affected by PC1. The others reflect anthropogenic activities and are identified by the combination of the three PCs.     

Geochemistry and stable isotopic composition of tufa waters and precipitates from the Interlake Region, Manitoba, Canada: Constraints on groundwater origin, calcitization, and tufa formation

New major, trace and isotopic geochemical results from a regional study of springs discharging from the major carbonate rock aquifer in the Interlake Region of Manitoba, Canada, are used to understand water–rock reactions, timing of recharge/discharge, tufa formation processes, and as baseline data. Spring waters are fresh with total dissolved solids (TDS) concentrations ranging from 150 to 880 mg/L. Waters discharging in the northern part of the study area have lower TDS, are dominantly Ca–Mg–HCO₃ waters with low SO₄ concentrations (<< 50 mg/L), and appear to have interacted primarily with Silurian carbonate lithologies. In contrast, waters in the southeastern part of the study area have higher TDS and have elevated SO₄ concentrations (up to 210 mg/L). Spring waters have elevated Mg/Ca_molar (1.23 ± 0.23), typically greater than congruent dissolution of dolomite. Ca and Mg concentrations and Mg/Ca_molar indicate that groundwater residence times were sufficient to allow equilibration with bedrock dolomite lithologies; elevated tritium in northern waters indicates a significant recharge component in the 1960's and 1970's. Tufa precipitates that have formed from many of the spring waters are low-Mg calcite (MgO = 1.70 to 5.80 wt.%). Sr concentrations are variable (57 to 657 ppm) and tufa Sr/Ca_molar ratios appear to be entirely controlled by spring water Sr/Ca_molar. Empirically determined Sr distribution coefficients (D_Sr = 0.389 ± 0.083) indicate rapid crystallization following CO₂ degassing, consistent with heavier δ¹³C_VPDB compared to spring waters. Sulfate concentrations are generally too low for calcitization (dedolomitization) reactions driven by anhydrite dissolution to be the dominant control on the elevated groundwater Mg/Ca_molar, implying either extensive sulfate reduction along the flow paths (however, δ¹³C_DIC suggests the elevated SO₄ is more consistent with Fe-sulfide oxidation), or that other processes are involved. Major ion ratios suggest that the waters in the southern part of the study area are more consistent with interaction with siliciclastic rocks than with anhydrite dissolution. We suggest that calcitization (dedolomitization) reactions driven by anhydrite dissolution may not dominate all carbonate aquifers and that mixing of waters in karst conduits combined with ion exchange reactions are important controls on water chemistry in these systems.     

Influence of volcanic activity on spring water chemistry at Popocatepetl Volcano, Mexico

The results of the 7 years (1994–2000) of monthly monitoring of spring water before and during eruptions show response to volcanic activity. Low salinity and temperature characterize most of the springs, which are located on the flanks of Popocatepetl Volcano. The pH ranges from 5.8 to 7.8 and temperature from 3 to 36 °C. Oxygen and hydrogen isotopic data show that the water is of meteoric origin, but SO₄²⁻, Cl⁻, F⁻, HCO₃⁻, B, and SO₄²⁻/Cl⁻ variations precede main eruptive activity, which is considered linked to influx of magmatic gases and acid fluids that react with sublimates and host rock and mix with the large water system. Na⁺, Ca²⁺, SiO₂ and Mg²⁺ concentrations in the water also increased before eruptive activity. The computed partial pressure of CO₂ in equilibrium with spring waters shows values higher than air-saturated water (ASW), with the highest values up to 0.73 bar of pCO₂. Boron is detected in the water only preceding the larger eruptions. When present, boron concentration is normally under health standard limits, but in two cases the concentration was slightly above. Other components are within health standard limits, except for F⁻ in one spring.     

The Petrology and Geochemistry of Calc-Alkaline Andesites on Shodo-Shima Island, SW Japan

Petrographical and geochemical characteristics of calc-alkalineandesites on Shodo-Shima Island, SW Japan, having bulk compositionslargely identical to the continental crust, are presented. Thefollowing petrographic observations suggest a role for magmamixing in producing such andesite magmas: (1) two types of olivinephenocrysts and spinel inclusions, one with compositions identicalto those in high-Mg andesites and the other identical to thosein basalts, are recognized in terms of Ni–Mg and Cr–Al–Fe³⁺relations, respectively; (2) the presence of orthopyroxene phenocrystswith mg-number >90 suggests the contribution of an orthopyroxene-bearinghigh-Mg andesite magma to production of calc-alkaline andesites;(3) reversely zoned pyroxene phenocrysts may not be in equilibriumwith Mg-rich olivine, suggesting the involvement of a differentiatedandesite magma as an endmember component; (4) the presence ofvery Fe-rich orthopyroxene phenocrysts indicates the associationof an orthopyroxene-bearing rhyolitic magma. Contributions fromthe above at least five endmember magmas to the calc-alkalineandesite genesis can also provide a reasonable explanation ofthe Pb–Sr–Nd isotope compositions of such andesites. KEY WORDS: calc-alkaline andesites; high-Mg andesites; magma mixing; continental crust; SW Japan     

Evaluation of formation water chemistry and scale prediction: Bakken Shale

Determination of in situ formation water chemistry is an essential component of reservoir management. This paper details the use of thermodynamic computer models to calculate reservoir pH and restore produced water analyses for prediction of scale formation. Bakken produced water samples were restored to formation conditions and calculations of scale formation performed. In situ pH is controlled by feldspar-clay equilibria. Calcite scale is readily formed due to changes in pH during pressure drop from in situ to surface conditions. The formation of anhydrite and halite scale, which has been observed, was predicted only for the most saline samples. In addition, the formation of anhydrite and/or halite may be related to the localized conditions of increased salinity as water is partitioned into the gas phase during production.     

Diagenesis and formation water chemistry of Triassic reservoir sandstones from southern Tunisia

The fluvial Triassic reservoir subarkoses and arkoses (2409·5–2519·45 m) of the El Borma oilfield, southern Tunisia, were subjected to cementation by haematite, anatase, infiltrated clays, kaolinite and K-feldspar at shallow burial depths from meteoric waters. Subsequently, basinal brines controlled the diagenetic evolution of the sandstones and resulted initially in the precipitation of quartz overgrowths, magnesian siderite, minor ferroan magnesite and anhydrite. The enrichment of siderite in ¹²C isotope (δ¹³C_PDB= - 14·5 to - 9‰) results from derivation of carbon from the thermal decarboxylation of organic matter. During further burial, the precipitation of dickite and pervasive transformation of kaolinite into dickite occurred, followed by the formation of microcrystalline K-feldspar and quartz, chlorite and illite, prior to the emplacement of oil. Present day formation waters are Na-Ca-Cl brines evolved by the evaporation of seawater and water/mineral interaction and are in equilibrium with the deep burial (≤ 3·1 km) minerals. These waters are suggested to be derived from the underlying Silurian and Devonian dolomitic mudstones.     

Temporal and spatial differences in salinity and water chemistry in SW Florida estuaries: Effects of human-impacted watersheds

Three estuaries near Naples, Florida with variably modified watersheds have been investigated to understand the chemical consequences of altering drainage patterns. Blackwater River (near natural drainage, control site), Henderson Creek (moderately modified watershed), and Faka-Union Canal (severe channelization) were sampled for temperature, salinity, δ¹⁸O, δ¹³C of dissolved inorganic carbon (DIC), molality of CO₂ (ΣCO₂), and Mg:Ca and Sr:Ca ratios between freshwater and marine water end members over a 17-mo period. Carbon isotope composition followed similar seasonal patterns as salinity. Freshwater and seawater end members are more negative than the global average, likely reflecting equilibration with local carbon sources derived from mangrove leaf litter and groundwater. δ¹³C responds to differences in primary productivity between estuaries. Henderson Creek has higher primary productivity than Blackwater River (probable due to higher sewage input and agricultural runoff) and has more positive δ¹³C and lower ΣCO₂. δ¹⁸O is affected by seasonal input of freshwater from atmospheric precipitation, evaporation, and groundwater. Late summer and fall rains lower the δ¹⁸O of estuarine water, whereas evaporative conditions in the dry season elevate δ¹⁸O to values that can be more positive upstream than those from the Gulf of Mexico (estuarine inversion). Evaporation produces water in the Gulf of Mexico that is >1‰ more positive than the global sea surface average most of the year. The very negative δ¹⁸O values in Blackwater River and Henderson Creek likely reflect atmospheric and groundwater contribution. Mg:Ca and Sr:Ca ratios of Gulf water from all three estuaries are similar to global averages at low latitudes. Freshwater end members among estuaries are different in that Blackwater River has higher ratios, suggesting a groundwater contribution. Dolomitic rocks in the subsurface likely provide a source of Mg ions.     

Diagenesis of the Lower Cretaceous Kanmon Group sandstones, SW Japan

The Kanmon Group (Lower Cretaceous) is a non-marine sequence in the Inner Zone of southwest Japan and is divided into the lower Wakino (lacustrine) and the upper Shimonoseki (fluvial) subgroups. Major diagenetic changes in this group are compaction, iron-oxide cementation, calcite cementation and grain replacement, quartz overgrowth and pore-fill cementation, illite authigenesis, chlorite pore-fill cementation and grain replacement, albitization of feldspar, and grain replacement by pyrite. Two subgroups of the Kanmon Group present no significant differences in general diagenetic features, paragenetic sequence, or the degree of diagenetic changes despite differences in depositional environments (lacustrine vs. fluvial) and stratigraphic positions. However, some differences are recognized in the content and chemistry of authigenic minerals caused by different sandstone framework compositions. The content of authigenic clay minerals is higher in sandstones of the Shimonoseki Subgroup containing abundant volcanic rock fragments. In addition, the composition of chlorite, the most abundant authigenic clay mineral in Kanmon sandstones, is Mg-rich in the volcanoclastic Shimonoseki sandstones, compared to an Fe-rich variety in Wakino sandstones. The original sandstone composition played a significant role in pore-water composition and diagenetic reactions.The Wakino sandstones lost most of its porosity by compaction, whereas Shimonoseki sandstones are only compacted in the vicinity of the basin-bounding fault. The weakly compacted Shimonoseki sandstones, instead, were largely cemented by pore-filling calcite during early diagenesis; cementation prevented compaction during further burial. The Kanmon Group sediments were heated to about 300 °C based on illite crystallinity values.     

Formation and mineral chemistry of a calcic skarn from Al-Madhiq, SW Saudi Arabia

A newly identified skarn occurrence is described from the Neoproterozoic rocks of the SW Arabian shield. It is exposed to the SE, E and NE of the Al-Madhiq town. The skarn attributes correspond to those typical of the calcic skarns that host W-deposits. It is characterized as an exoskarn of the proximal type, related to a granitoid contact close to an impure quartzite bed within the regional metamorphic rocks of mixed sedimentary and volcanic derivation. The skarn is localized along a shear zone parallel to the regional faults and other major shear zones. Samples from the studied area contain characteristic skarn minerals that include both the prograde (brownish red grossular, ferrosalite, aluminian titanite-grothite, albite-oligoclase, scapolite), and retrograde (epidote, quartz, hornblende, calcite) assemblages. The pyroxenes are ferrosalites, Mn-bearing, and more like those from “oxidized” skarns; although garnets indicate it to be a “reduced” type skarn. Epidote mimicks that from typical skarns, as it bears a pistacite content of 15.9–20.7%. Grossular composition reflects a largely reduced genetic environment; as it is in solid solution with 6.5–21.6% andradite, 0–0.15% uvarovite, 0–0.47% pyrope, 4.33–18.75% almandine, and 0.4–8.58% spessartine molecules. Titanite composition varies from aluminian titanite to grothite, that may be analogous to the newly described Al-rich titanite from the low-pressure calc-silicate rocks.     

Boron in metapelites controlled by the breakdown of tourmaline and retrograde formation of borosilicates in the Yanai area,Ryoke metamorphic belt,SW Japan

Tourmaline-out isograd formed by the breakdown of tourmaline is defined in the upper amphibolite-facies metapelites in the Yanai area, Ryoke metamorphic belt, SW Japan. The rim composition of tourmaline progressively becomes aluminous with ascending metamorphic grade, and the chemical zoning of tourmaline is controlled by ^X□AlNa_–1Mg_–1 and MgTi^YAl_–2 vectors in low- to medium-grade zones where muscovite is stable, whereas it is controlled by Mg(OH)^YAl_–1O_–1, CaMgO^X□_–1 ^YAl_–1(OH)_–1 and MgTi^YAl_–2 vectors in further higher–grade, muscovite-unstable zones. The size of tourmaline increases drastically where breakdown of muscovite+quartz takes place, probably due to the growth of tourmaline during breakdown of muscovite. On the high-temperature side of the tourmaline-out isograd, depletion of whole-rock boron is observed. Escape of boron-bearing melt or the fluid evolved from the melt during its crystallization probably caused this depletion, although locally trapped, boron-bearing melt or fluid formed irregularly shaped tourmaline and dumortierite during retrograde metamorphism.     

Paragenesis and conditions of formation of the Moschellandsberg mercury deposit,SW Germany

The Moschellandsberg mercury deposit (SW Germany) is hosted in a Permo-Carboniferous volcanic caldera and has formed at shallow depths (100–300 m) and over a wide temperature range from about 200°C to less than 65°C. The deposit shows vertical zonation and the mineral paragenesis is unusually complex and contains significant amounts of Sb, As, Cu, and Ag. Fahlores are Hg-and Fe-rich Sb (Bi) and As members displaying a mixing gap. Vesicular ore textures and limited fluid inclusion evidence prove the existence of an immiscible gas phase during ore deposition. The fluid composition can be constrained to pH4, H₂S10^–5 molal, CO₂10^–1 molal, and f_H210^–2–10^–3 bar by comparing the observed mineral associations with stable phase assemblages calculated from thermodynamic data. Calculated metal solubilities indicate that Hg, Ag, and Sb can be transported very efficiently in such a fluid, but that the solubility of gold is very low.     

Age constraints on Tarkwaian palaeoplacer and lode-gold formation in the Tarkwa-Damang district, SW Ghana

Two major epigenetic gold-forming events are recorded in the world-class gold province of southwest Ghana. A pre-Tarkwaian event was the source of the world-class Tarkwa palaeoplacers whereas post-Birimian and Tarkwaian deformation, which was related to the Eburnean orogeny, gave rise to the world-class (e.g. Prestea) to giant (e.g. Obuasi) orogenic gold deposits which have made the region famous for more than 2,500 years. A maximum age of 2133±4 Ma for Tarkwaian sedimentation is provided by 71 of 111 concordant SHRIMP II U–Pb dates from detrital zircons in Tarkwaian clastic rocks from Damang and Bippo Bin, northeast of Tarkwa. The overall data distribution broadly overlaps the relatively poorly constrained ages of Birimian volcanism and associated Dixcove-type granitoid emplacement, indicating syntectonic development of the Tarkwaian sedimentary basin. These zircon ages argue against derivation of the palaeoplacer gold from an orogenic gold source related to the compressional phase of an orogeny significantly older than the Eburnean orogeny. Instead, they suggest that the gold source was either orogenic gold lodes related to an earlier compressional phase of a diachronous Eburnean orogeny or ca. 2200–2100 Ma intrusion-related gold lode. The CO₂-rich fluid inclusions in associated vein-quartz pebbles are permissive of either source. At the Damang deposit, an epigenetic, orogenic lode-gold system clearly overprinted, and sulphidised low-grade palaeoplacer hematite–magnetite gold occurrences in the Banket Series conglomerate within the Tarkwaian sedimentary sequence. Gold mineralisation is demonstrably post-peak metamorphism, as gold-related alteration assemblages overprint metamorphic assemblages in host rocks. In alteration zones surrounding the dominant, subhorizontal auriferous quartz veins, there are rare occurrences of hydrothermal xenotime which give a SHRIMP U–Pb age of 2063±9 Ma for gold mineralisation. The similar structural timing of epigenetic gold mineralisation in Tarkwaian host rocks at Damang to that in mainly Birimian host rocks elsewhere in southwest Ghana, particularly at Obuasi, suggests that 2063±9 Ma is the best available age estimate for widespread orogenic gold mineralisation in the region. Argon–argon ages of 2029±4 and 2034±4 Ma for hydrothermal biotite from auriferous quartz veins appear to represent uplift and cooling of the region below about 300 °C, as estimates of the temperature of gold mineralisation are higher, at around 400 °C. If peak metamorphism, with temperatures of about 550 °C, is assumed to have occurred at about 2100 Ma, the biotite ages, in combination with the xenotime age, suggest a broadly constant uplift rate for the region of about 1 km per 10 million years from about 2100 to 2025 Ma.     

Influence of arsenic-bearing gold deposits on water quality in Zloty Stok mining area (SW Poland)

 The Sudety Mountains contain polymetallic deposits which have been exploited since the Middle Ages. Distinct concentrations of As, Hg, F, Cr in surface water near Zloty Stok suggested that groundwater in the area could also contain elevated metal concentrations. Water samples from 15 locations including Zloty Stream, mine adit discharges, and selected springs generally show low levels of dissolved components and near-neutral pH. However, arsenic concentrations range from 0.99 mg/l to 26.16 mg/l at all 15 sample locations. Mercury concentrations were locally as high as 0.011 mg/l. These high arsenic and mercury concentrations significantly exceed water quality standards and raise concerns for using Zloty Stream for potable water. Recieved: 21 December 1998 · Accepted: 8 June 1999     

Pressure-temperature conditions of the Ryoke metamorphic rocks in Yanai district,SW Japan

Pressure-temperature conditions of metamorphism in the Yanai district, Ryoke belt, SW Japan, have been determined using garnet-biotite thermometry in combination with an empirically calibrated barometer in the assemblage common in pelitic and siliceous rocks, garnet + biotite + plagioclase + quartz. The barometer estimates pressure difference between a well-established sample and unknown samples based on the reaction,

滇西老王寨金矿床黄铁矿形貌特征与化学组成

老王寨金矿床是三江特提斯成矿域中已探明规模最大的造山型金矿床,黄铁矿是其最主要的载金矿物,依据矿(化)脉切割关系、矿石结构构造及矿物共生组合,该矿床成岩-成矿期共发育5个世代黄铁矿。沉积-成岩期草莓状黄铁矿含Pb、Zn、Mn、Co、Ni和Bi。热液金成矿期可划分为:Ⅰ石英-绢云母-黄铁矿、Ⅱ石英-多金属硫化物、Ⅲ方解石-石英-毒砂-黄铁矿和Ⅳ方解石-石英-辉锑矿-黄铁矿四个阶段,其黄铁矿分别以粗粒他形、立方体、五角十二面体和立方体为主,总体继承了沉积-成岩期黄铁矿含Pb、Zn、Mn、Co、Ni和Bi的特征,Au、As、Sb和Cu也有不同程度富集,显示成矿流体成分复杂。Ⅲ阶段为金的主成矿阶段,以发育五角十二面体黄铁矿为特征,富集Au、As、Sb、Pb、Zn、Cu、Co、Ni和Bi,其中,Au与As构成 [Au, As]^2-和[Au(As, S₃)]^2-等络合物以类质同象的形式替代[S²]^2-而进入到黄铁矿中,两者呈正相关,成矿系统处于中-低温、流体过饱和度(硫逸度)高,且缓慢冷却,矿质来源充足的环境。     

Ion chemistry of groundwater and the possible controls within Lhasa River Basin,SW Tibetan Plateau

In order to study the major ion chemistry and controls of groundwater, 65 groundwater samples were collected and their major ions measured from wells within Lhasa River Basin. Groundwater has the characteristics of slightly alkaline and moderate total dissolved solid (TDS). TDS concentration ranged from 122.0 to 489.9 mg/L with a median value of 271.2 mg/L. Almost all the groundwater samples suited for drinking and irrigation. The major cations of groundwater are Ca²⁺ and Mg²⁺, accounting for 59.6 and 31.3% of the cations, respectively. Meanwhile, HCO₃^? and SO₄^2? constituted about 56.7 and 36.9% of the anions, respectively, in Lhasa River Basin. The hydrochemical type of groundwater is HCO₃-SO₄-Ca-Mg. The chemical composition of groundwater samples located in the middle of Gibbs model, which indicates that the major chemical process of groundwater is controlled by rock weathering. Carbonate weathering was the dominant hydro-geochemical process controlling the concentration of major ions in groundwater within Lhasa River Basin, but silicate weathering also plays an important role.