Contrasting stable isotope behavior between calcite and dolomite marbles,Lone Mountain,Nevada

 Late Proterozoic to Cambrian carbonate rocks from Lone Mountain, west central Nevada, record multiple post-depositional events including: (1) diagenesis, (2) Mesozoic regional metamorphism, (3) Late Cretaceous contact metamorphism, related to the emplacement of the Lone Mountain granitic pluton and (4) Tertiary hydrothermal alteration associated with extension, uplift and intrusion of silicic porphyry and lamprophyre dikes. Essentially pure calcite and dolomite marbles have stable isotopic compositions that can be divided into two groups, one with positive δ¹³C values from+3.1 to +1.4 ‰ (PDB) and high δ¹⁸O values from +21.5 to +15.8 ‰ (SMOW), and the other with negative δ¹³C values from –3.3 to –3.6‰ and low δ¹⁸O values from +16.9 to +11.1‰. Marbles also contain minor amounts of quartz, muscovite and phlogopite. Brown and blue luminescent, clear, smooth textured quartz grains from orange luminescent calcite marbles have high δ¹⁸O values from +23.9 to +18.1‰, while brown luminescent, opaque, rough textured quartz grains from red luminescent dolomite marbles typically have low δ¹⁸O values from +2.0 to +9.3‰. The δ¹⁸O values of muscovite and phlogopite from marbles are typical of micas in metamorphic rocks, with values between +10.4 and +14.4‰, whereas mica δD values are very depleted, varying from −102 to −156‰. No significant lowering of the δ¹⁸O values of Lone Mountain carbonates is inferred to have occurred during metamorphism as a result of devolatilization reactions because of the essentially pure nature of the marbles. Bright luminescence along the edges of fractures, quartz cements and quartz overgrowths in dolomite marbles, low δD values of micas, negative δ¹³C values and low δ¹⁸O values of calcite and dolomite, and depleted δ¹⁸O values of quartz from dolomite marbles all indicate that meteoric fluids interacted with Lone Mountain marbles during the Tertiary. Partial oxygen isotopic exchange between calcite and low ¹⁸O meteoric fluids lowered the δ¹⁸O values of calcite, resulting in uniform quartz-calcite fractionations that define an apparent pseudoisotherm. These quartz-calcite fractionations significantly underestimate both the temperature of metamorphism and the temperature of post-metamorphic alteration. Partial oxygen isotopic exchange between quartz and meteoric fluids also resulted in ¹⁸O depletion of quartz from dolomite marbles. This partial exchange was facilitated by an increase in the surface area of the quartz as a result of its dissolution by meteoric fluids. The negative δ¹³C values in carbonates result from the oxidation of organic material by meteoric fluids following metamorphism. Stable isotopic data from Lone Mountain marbles are consistent with the extensive circulation of meteoric hydrothermal fluids throughout western Nevada in Tertiary time. Received: 1 February 1994/Accepted: 12 September 1995     

Fe and Al oxides distribution in some ultisols and inceptisols of southeastern Nigeria in relation to soil total phosphorus

Ten highly weathered soils in southeastern Nigeria were sampled from their typical A and B horizons for analyses. The objectives were to determine the different forms of Fe and Al oxides in the soils and relating their occurrence to phosphate availability and retention in the soils. The soils are deep and often physically degraded but are well drained and coarse in the particle size distribution. They are mostly dominated by kaolinite in their mineralogy with very high values of SiO₂. The soils are acidic with low soil organic carbon (SOC) contents. The elements in the exchange complex are also low thus reflecting in the low CEC of the soil. Available phosphorus (P) in the soils are generally low while total P ranged from 157 to 982 mg kg⁻¹ with an overall average of 422 mg kg⁻¹. Total Fe in the soil is highest and their order represented as follows: Fe_t > Fe_d > Fe_ox ≥ Fe_p. The pyrophosphate extractable Fe was always higher in the top soil than in the subsoil and was attributed to the fact that these forms of Fe are associated with organic matter which is more abundant in topsoil than in subsoil. Like in Fe forms, the order of Al occurrence could generally be presented as; Al_t > Al_d > Al_ox > Al_p. More Fe and Al oxides in the soils are strongly crystalline while a small quantity is poorly crystalline Fe forms. The amorphous forms of both Fe and Al are very low in the soils when compared with the crystalline forms. The oxides that show very strong affinity to total P are Fe_d–Fe_ox, Fe_d, Al_d, Fe_t, Fe_ox and Al_ox/Al_d. To overcome this problem of P retention in the soil, we recommend constant liming of these soils to neutralize them, application of organic matter and of high dosage of phosphate fertilizer to the soils.     

The effect of distribution of iron-oxyhydroxide grain coatings on the transport of bacterial cells in porous media

 Among the demonstrated processes influencing the transport of bacteria through aquifers, the deposition of cells on mineral surfaces is one of the most important. For example, understanding the transport of introduced bacteria through aquifers is essential to designing some in situ bioremediation schemes. The impact of the presence and distribution of Fe(III)-oxyhydroxide-coated sand grains on bacterial transport through porous media was evaluated in column experiments in which bacteria (short rods; 1.2 μm length) were eluted through columns of quartz sand (0.5–0.6 mm in diameter) for several conditions of chemical heterogeneity of mineral substrate. Fe(III)-oxyhydroxide-coated sand was present as 10% of the mass, and it was arranged in three treatments: (1) homogeneously distributed, and present as a discrete layer (2) at the top and (3) at the bottom of 14-cm-long sand columns. A pulse input of 10⁸ cells ml^–1 was introduced in an artificial groundwater solution flowing at 14 cm h^–1 through the column, and eluted cells were counted. Peak breakthrough occurred at 1.0 pore volume. A large proportion of cells were retained; 14.7–15.8% of the cells were recovered after three pore volumes of solution had eluted through clean quartz sand, and only 2.1–4.0% were recovered from the Fe(III)-oxyhydroxide-coated sand mixtures. The three physical arrangements of the chemical heterogeneity resulted in essentially the same breakthrough of cells, indicating that the spatial distribution of iron coating does not affect the transport of bacteria. The results of the column transport experiments, which mimic hydrogeological conditions encountered in field problems, are consistent with our mechanistic understanding of bacterial sorption. Received: 10 April 1996 · Accepted: 17 February 1997     

Implications from inclusions in topaz for greisenisation and mineralisation in the Hensbarrow topaz granite, Cornwall, England

Textural and geochemical studies of inclusions in topaz from greisens in the Hensbarrow topaz granite stock (St. Austell, Cornwall) are used to constrain the composition of fluids responsible for late stage greisening and mineralisation. The topaz contains an abundant and varied suite of inclusions including aqueous liquid + vapour (L + V), quartz, zinnwaldite, albite, K-feldspar, muscovite, ilmenorutile, apatite, columbite, zircon, varlamoffite [(Sn, Fe)(O, OH)₂] and qitianlingite [(Fe⁺²,Mn⁺²)₂(Nb,Ta)₂W⁺⁶O₁₀]. Primary L + V inclusions in topaz show relatively high T _h (mainly 300 to >500 °C) and a narrow range of salinities (23–30 wt % NaCl equivalent) compared with those in greisen quartz (150–450 °C, 0–50 wt % NaCl equivalent). Textures indicate that topaz formed earlier than quartz and the fluid inclusion data are interpreted as indicating a cooling of the hydrothermal fluids during greisenisation, mixing with meteoric waters and a decrease in pressure causing intermittent boiling. The presence of early-formed albite and K-feldspar as inclusions in the topaz is likely to indicate that the greisen-forming fluid became progressively more acid during greisenisation. The most distinctive inclusions in the topaz are wisp- and bleb-shaped quartz, < 50 μm in size, which show textural characteristics indicating former high degrees of plasticity. They often have multiple shrinkage bubbles at their margins rich in Sn, Fe, Mn, S and Cl and, more rarely, contain euhedral albite, K-feldspar, stannite or pyrrhotite crystals up to 40 μm in size. The quartz inclusions show similar morphologies to inclusions in topaz from quartz-topaz rocks elsewhere which have been interpreted as trapped “silicate melt”. Their compositions are, however, very different to those expected for late stage topaz-normative granitic melts. From their textural and chemical characteristics they are interpreted as representing crystallised silica colloid, probably trapped as a hydro gel during greisenisation. There is also evidence for the colloidal origin of inclusions of varlamoffite in the topaz. These occurrences offer the first reported evidence in natural systems for the formation of colloids in high temperature hydrothermal fluids. Their high ore carrying potential is suggested by the presence of varlamoffite and the occurrence of stannite, pyrrhotite and SnCl within the quartz inclusions. Received: 9 April 1996 / Accepted: 12 November 1996     

Mineralogy and origin of stichtite in chromite-bearing serpentinites

Stichtite, a rare (14 known localities worldwide) hydrated carbonate-hydroxide of Mg and Cr with ideal formula Mg₆Cr₂ (OH)₁₆ CO₃ · 4H₂O, occurs exclusively in Cr-rich serpentinites of ophiolites or greenstone belts. Physical properties (hardness = 1.5–2, specific gravity = 2.16–2.2, perfect basal [0001] cleavage, grain size commonly < 100 μm) resemble talc, but the mineral has an attractive purple to lilac color; chemical analyses demonstrate it to be a non-silicate. Stichtite generally occurs as irregular to rounded masses (< 1 cm – 30 cm across) and as veinlets (< 1 mm – > 2 cm wide) within serpentinite. Macroscopic and microscopic textures, such as crosscutting veinlets and stringers, demonstrate that stichtite formation invariably post-dated serpentinization. In some specimens stichtite surrounds relict grains of Cr-rich spinel; in others stichtite has completely replaced euhedral or subhedral chromites. Chemical analyses of stichtites reveal substantial substitution of Al and Fe³⁺ for Cr in specimens from many localities, reflecting a possible compositional continuum between stichtite and rhombohedral polymorphs hydrotalcite (Mg₆Al₂ (OH)₁₆ CO₃ · 4H₂O) and pyroaurite (Mg₆Fe₂ (OH)₁₆ CO₃ · 4H₂O). We report the first electron microprobe analyses of stichtites from seven localities, and summarize all available published chemical data. Stichtites very likely inherited part of their trivalent cation chemistry from precursor Cr-rich spinels, but stichtite growth apparently post-dated characteristic “ferritchromit” alteration, as demonstrated by the depletion of Al and enrichment in Fe³⁺ in stichtite relative to primary chromite core compositions. Stichtite appears to form by reaction between serpentine and altered chromite, during addition of substantial fluid, either as separate H₂O and CO₂ phases, or as a mixed volatile phase. Such reactions must involve removal of substantial SiO₂, possibly by transport and remote deposition of silica by throughgoing aqueous and carbonic fluid. Received: 4 April 1996 / Accepted: 16 September 1996     

The Malanjkhand copper ( + molybdenum) deposit, India: mineralization from a low-temperature ore-fluid of granitoid affiliation

  Copper and subordinate molybdenum mineralization at Malanjkhand occurs within a fracture-controlled quartz-reef enclosed in a pink granitoid body surrounded by grey-granitoids constituting the regional matrix. Sulfide-bearing stringers, pegmatites with only quartz + microcline and sulfide disseminations, all within the pink-granitoid, represent other minor modes of occurrences. Despite this diversity in mode of occurrence, the mineralogy of ores is quite consistent and conform to a common paragenetic sequence comprising an early `ferrous' stage of precipitation of magnetite (I) and pyrite (I) and, the main-stage chalcopyrite mineralization with minor sphalerite, pyrite (II), magnetite (II), molybdenite and hematite. Both stages witnessed continuous precipitation of quartz ± microcline ± (chlorite, biotite and epidote). The enclosing pink-granitoid and the regional grey-granitoids display alteration features such as saussuritization of plagioclase, breakdown of hornblende and chloritization of biotite on a regional scale, indicating interaction with a pervasive fluid. Quartz and microcline precipitation mostly restricted within the pink granitoid, postdates this alteration. Four types of primary inclusions were encountered in quartz from ore samples: (1) type-I – aqueous-biphase(L + V) inclusions, the commonest variety in all ore types; (2) type-II – aqueous-carbonic(L_aq + L_carb ± V_carb); (3) type-III – pure-carbonic(L_carb ± V_carb) – type-II and III being restricted to stringer and pegmatitic ores, and (4) rare polyphase (L_aq + V_aq + calcite/gypsum) inclusions. Quartz in granitoids contain primary type-I inclusions only. Type-I inclusions from ore samples furnish a temperature range (after a rough pressure correction to the T _H  -maxima of 140–180 °C) of 150–275 °C and a moderately low salinity of 4–12 wt.% NaCl equivalent. This is inferred to represent the signature of the major component (F2) of the ore fluid. A few type-I inclusions of higher T _M (up to 380 °C) and low salinity and density represent the other (F1) identifiable component of the ore fluid present in low proportion. The T _H  -maxima and the total range in salinity of type-I inclusions in quartz from granitoids are strikingly similar to those from the ore samples. Composition of syn-ore chlorites furnished a temperature range of 185–327 °C, which conforms to the fluid inclusion microthermometric data. Pressure estimates using standard fluid inclusion geobarometric methods, vary from 550 to 1790 bar in the stringer ores. Observed temperature-salinity/density relationships are best explained by a two-stage evolution model of the ore fluid: the first stage witnessed mixing of the two components, F1 and F2 in unequal proportion, bringing about mineralization. The second stage of evolution was marked by the separation of a carbonic component on continued sulfide precipitation and attendant increase in salinity of the fluid. The F1 component emerged as a distinct, heated and (CO₂ + S)-charged entity due to steam-heating and contamination of the early-ingressed F2 fluid at the fracture zone. The pervasive fluid phase in the surrounding granitoids contributed the F2 component. Received: (10 August 1994), 15 August 1995 / Accepted: 12 January 1996     

图门江下游沙丘粒度分布与石英表面结构研究

图门江下游沙丘粒度频率累积曲线形态全部为双峰,负偏态,粒度变化范围大,平均粒度数值小,标准偏差平均值为0.61;粒度分布特征方法判断沙丘沉积环境以河流成因为主。通过扫描电镜研究其石英颗粒表面结构,机械作用以贝壳状断口、V形坑和次棱角状形态组合为主,化学作用为中等-强烈溶蚀特征;石英颗粒表面结构特征表明沙丘为河口沉积;热释光测年结果表明沙丘受全新世海平面变化的影响,经历海水及风力改造。     

A new locality of palygorskite-rich clay from the southeastern Yucatán: a potential material source for environmental applications

A palygorskite unit was discovered in a road cut of undifferentiated Tertiary limestone between the villages of El Pariso and San Roman (18°49.309N, 88°37.861W) in the southeastern Yucatán Peninsula, Mexico. This is the southern most locality of a clay-rich sedimentary unit reported in the literature for the Tertiary carbonates of the Yucatán Peninsula. This occurrence indicates a much wider range of palygorskite-rich clay deposition than previously recognized. The lithology is 99% clay and 1% sand to silt size diagenetic quartz grains. The clay consists of approximately 85% palygorskite, 15% montmorillonite and trace amounts of titanium oxides. EDS analyses on palygorskite are largely consistent with sedimentary palygorskites from other coastal marine settings, however palygorskite has a low total Fe content (average = 0.40 wt% expressed as Fe₂O₃) compared to many other sedimentary palygorskites. Montmorillonite chemical compositions are typical and compared to the palygorskite have substantially higher Fe₂O₃ concentrations (average = 3.90 wt%). The low percentage of coarse grains in the lithology combined with a high proportion of palygorskite and lack of detrimental trace minerals suggest the deposit is of industrial grade; however, it has limited reserves (6,000 m³). The unit could be potentially used in a wide array of environmental applications which are needed in the region including liners for landfills and constructed wetlands. The unit is in a geographic location which would serve the expanding economy of the region. This resource has the potential to have great impact on the quality of the local environment and the economy of a region under great environmental threat.     

Adsorption of arsenic by natural aquifer material in the San Antonio-El Triunfo mining area, Baja California, Mexico

 Several experiments of arsenic (As) adsorption by aquifer material of the San Antonio-El Triunfo (SA-ET) mining area were conducted to test the feasibility of this material acting as a natural control for As concentrations in groundwater. This aquifer material is mineralogically complex, composed of quartz, feldspar, calcite, chlorite, illite, and magnetite/hematite. The total iron content (Fe₂O₃) in the fine fraction is ∼12%, whereas Fe₂O₃ in the coarse fraction is <10 wt%. The experimental percent total As adsorbed vs. pH curves obtained match the topology of total As adsorbed onto iron oxi-hydroxides surface (arsenate + arsenite; high adsorption at low pH, low adsorption at high pH). A maximum of about 80% adsorbed in the experiments suggests the presence of arsenite in the experimental solutions. The experimental adsorption isotherm at pH 7 indicates saturation of surface sites at high solute concentrations. Surface titration of the aquifer material indicates a point of zero charge (PZC) for the adsorbent of about 8 to 8.5 (PZC for iron oxyhydroxides =7.9–8.2). Comparison between experimental and modeled results (using the MICROQL and MINTEQA2 geochemical modeling and speciation computer programs) suggests that As is being adsorbed mostly by oxyhydroxides surfaces in the natural environment. Based on an estimated retardation factor (R), the travel time of the As plume from the SA-ET area to La Paz and Los Planes is about 700 to 5000 years. Received: 17 March 1997 · Accepted: 8 September 1997     

Metal contamination and filtering in soil from an iron (magnetite) mine–smelter complex in the critical Hudson Highlands watershed,New York

Organic material in metal contaminated soils around an abandoned magnetite mine–smelter complex in the critical Highlands watershed protects the groundwater and surface water from contamination. Metals in these waters were consistently below local and national water standards. Two groups of soil types cover the area: (1) Group A disturbed metal-rich soils, and (2) Group B undisturbed organic soils. Chromium and nickel were more elevated than other metals with Cr more widespread than Ni. In Group A, Cr correlated strongly with sesquioxides in the lower horizons (Fe₂O₃: r = 0.74, p < 0.025; Al₂O₃: r = 0.92, p < 0.005). In Group B, Cr correlated strongly (r = 0.96, p < 0.005) with soil organic matter (SOM) in the O-horizons. Ni–Cr (Group A: 52 and 70% in O- and lower horizons, respectively; Group B: ~100% in both horizons) and V–Cr correlations (78% only in Group A lower horizons) suggest similar retention mechanisms for these elements. Average soil \textpH_\textCaCl2 {\text{pH}}_{{{\text{CaCl}}_{2} }} for both groups ranged between 3.65 and 5.91, suggesting that soil acidity is determined by organic acids and solubility of Al³⁺ releasing H⁺ ions. SOM and sesquioxides contribute significantly to creating naturally occurring filtration systems, removing metals, and protecting water quality. High Ca, Fe, and Ti in Group A soils suggest slag and ash were mixed into the soils. Some low-Cr sources include magnetite, slag, and ash (100, 100 and 200 mg/kg, respectively). Constant ZrO ₂ :TiO ₂ ratios in the lower soils indicate soil formation from breakdown of underlying tailing rocks, contributing Cr to these layers.     

Field investigation of surface sand and dust movement over different sandy grasslands in the Otindag Sandy Land,China

The characteristics of sand and dust movement over different sandy grasslands in China’s Otindag Sandy Land were explored based on field observations and laboratory analyses. Threshold wind speeds (the speed required to initiate sand movement) at a height of 2 m above the ground were estimated in the field for different surface types. Threshold wind speed above shifting dunes in the study area is about 4.6 m s⁻¹ at this height. This value was smaller than values observed above other surfaces, resulting in a greater risk of blowing sand above these dunes. Differences in sand transport rates (STR) as a function of the severity of desertification resulted primarily from differences in surface vegetation cover and secondarily from the soil’s grain-size distribution. STR increased exponentially with increasing near-bed wind velocity. Under the same wind conditions, STR increased with increasing severity of desertification: from 0.08 g cm⁻² min⁻¹ above semi-fixed dunes to 8 g cm⁻² min⁻¹ above semi-shifting dunes and 25 g cm⁻² min⁻¹ above shifting dunes. Vegetation’s affect on STR was clearly large. Different components of sand and dust were trapped over different lands: mostly sand grains but little dust were trapped above shifting dunes, but much dust was collected over semi-shifting and semi-fixed dunes. Human disturbance is likely to produce dust even from fixed dunes as a result of trampling by animals and vehicle travel. In addition, spring rainfall decreased the risk of sand and dust movement by accelerating germination of plants and the formation of a soil crust.     

Valence state mapping and quantitative electron spectroscopic imaging of exsolution in titanohematite by energy-filtered TEM

 The microstructure of hematite-ilmenite exsolution intergrowth of a natural titanohematite crystal from a granulite has been investigated in a transmission electron microscope equipped with an energy filter. Special emphasis is on quantitative compositional mapping at the nanometre scale using electron spectroscopic imaging, as well as mapping the Fe³⁺ and Fe²⁺ valence distribution in the intergrowth. Quantitative point analyses by energy-dispersive X-ray analysis have been compared with results from electron energy-loss spectroscopy and element-distribution mapping. The results indicate that the coexisting compositions of the two phases (Ilm₈₈Hem₁₂ and Ilm₁₆Hem₈₄) are independent of the size of the exsolution. The application of quantitative mapping to determining diffusion profiles around precipitates is demonstrated. Received: 30 March 2000 / Accepted: 7 September 2000     

Effects of quarry mining and of other environmental impacts in the mountainous Chicam-Toctina drainage basin (Córdoba, Argentina)

 The environmental conditions prevailing in the Chicam-Toctina drainage system (approx. 138 km² in Córdoba, Argentina) are considered representative of a number of catchments in Argentina's Sierras Pampeanas Range. Two groups of ions reflect the sources of dissolved species in the catchment: a) a group (Cl^–, SO^2– ₄, and Na⁺) which recognizes natural and anthropogenic sources, and which exhibits significant correlations with N^– ₃ and NO^– ₂, and b) another group of components (Ca²⁺, Mg²⁺, and HCO^– ₃) which is clearly controlled by carbonate rocks and their waste rock products. In the headwaters, stockpiled marble quarry mining wastes provide a more open system to CO₂ gaseous exchange than the outcropping rocks, thus promoting the increase of carbonate dissolution (up to 4.88 g km^–2 s^–1 during the rainy season). This specific yield was 20% higher than the amount estimated for an area with fewer extended mining activities. The dissolved load delivered by the upper reaches is subjected in the lower drainage area to various processes, mainly controlled by the presence of the city of Alta Gracia (approx. 40,000 inhabitants). In the dry season, due to nutrient inputs supplied by the city, photosynthetic activity plays a major role controlling stream pH. Hence, the high values of calcite saturation indexes and the increase of CaCO₃ concentration in bed sediments can be explained by calcite precipitation. Such a process could be accompanied by the coprecipitation on calcium carbonate of low solubility heavy metal carbonates. Received : 17 January 1997 · Accepted : 31 March 1997     

A theoretical investigation of the relative stabilities of Fe-free clinozoisite and orthozoisite

 The relative stabilities of orthozoisite, Ca₂Al₃[O|OH|Si₂O₇|SiO₄], space group Pnma, and the monoclinic polymorph, clinozoisite, space group P2₁/m, have been investigated using calculations based on density functional theory. It is found that orthozoisite is more stable than clinozoisite by about 1 kJ mol⁻¹ at zero pressure in the athermal limit. The bulk moduli of the two polymorphs have been calculated to be B_ortho=117.5(1.7) GPa and B_clino=136(4) GPa. Received: 20 March 2000 / Accepted: 26 February 2001     

Stability of aggregates of some weathered soils in south-eastern Nigeria in relation to their geochemical properties

The stability of some highly weathered soils of the tropics is controlled by their organo-mineral substances. Highly weathered soils from 10 different locations were sampled from their A and B horizons to determine their aggregate stability. The objective of the study was to determine the aggregate stability of the soils and their relationships with geochemical constituents. The major geochemical elements of the soils are quartz and kaolinite, SiO₂, Al₂O₃ and Fe₂O₃, while the dithionite extractable Fe and Al was greater than their corresponding oxalate and pyrophosphate forms. The mean-weight diameter from dried aggregates (MWD_d) and their corresponding wet mean-weight diameter (MWD_w) were related significantly (r = 0.64*). The dithionite extracted Al and Fe or the crystalline forms of these elements were outstanding in the stability of the aggregates. However, this did not diminish the influence of SOC reduced to third order level in the stability of the soils. The influence of SOC in these soils, however, indirectly manifested on the role of Fe_p and Al_p in the aggregation of these soils. The crystalline Fe and Al sesquioxides were very prominent in the aggregation and stability of these soils.     

Environmental hydrogeology of the southern sector of the Samborombon Bay wetland,Argentina

The Samborombon Bay wetland is located on the west margin of the Rio de la Plata estuary, in the Province of Buenos Aires, Argentina. This paper analyses the geological, geomorphologic, soil and vegetation characteristics of the southernmost sector of this wetland and their influence on surface water and groundwater. The study area presents three hydrologic units: coastal dunes, sand sheets and coastal plain. Coastal dunes and sand sheets are recharge zones of high permeability with well-drained, non-saline soils, and a few surface water flows. Changes in the water table are related to rainfall. Groundwater in coastal dunes is Ca–Mg–HCO₃ to Na–HCO₃, and of low salinity (590 mg/l). Groundwater in sand sheets is mainly Na–HCO₃ with a salinity of about 1,020 mg/l. The coastal plain exhibits medium to low permeability sediments, with submerged saline soils poorly drained. Groundwater is Na–Cl with a mean salinity of 16,502 mg/l. A surface hydrological network develops in the coastal plain. Surface water levels near the shoreline are affected by tidal fluctuations; far from the shoreline water accumulates because of poor drainage. Both sectors have Na–Cl water, but the former is more saline. Human intervention and sea level rise may affect the wetland severely.     

The formation of columnar fiber texture in wollastonite rims by induced stress and implications for diffusion-controlled corona growth

 The evolution of columnar fiber texture was studied in wollastonite reaction rims synthesized by the reaction calcite + quartz=wollastonite + CO₂. Experiments were performed at 850 to 950 °C at 100 MPa in dry CO₂ and were evaluated by scanning and transmission electron microscopy. Rim growth rates are interpreted as controlled by the diffusion of the SiO₂ component through the rims from the quartz–wollastonite to the wollastonite–calcite interface. The temperature dependence of rim growth rates yields an apparent activation energy of 314 ± 53 kJ mol⁻¹. The columnar fibrous wollastonite crystallizes at the quartz–wollastonite interface and comprises the largest parts of the rims. Ultimately, at the growth front strain contrast centers are present in the quartz. The strained volume extends about 200 nm into the quartz grains. We suggest that this might signify deformation of the quartz lattice due to wollastonite crystallization. Wollastonite fiber thickness was measured from TEM images along traverses that represent intermediate positions of the growth front during the experiments. The average thickness is in the 100–200 nm range. Fiber thickness increases with increasing growth temperature. At a given temperature, the thickness of the fibers at the growth front slightly decreases with time, i.e., the number of fiber tips per unit area in the growth front increases. The decrease of the fiber thickness is well fitted by a parabolic rate law. The generation of the columnar fiber texture is interpreted as an effect of induced stresses at the growth front, resulting from the volume increase due to the local reaction. This volume increase forces SiO₂ to diffuse along the growth front to the grain boundaries between the wollastonite fibers. These serve as fast diffusion pathways through the rims. The fiber thickness monitors the diffusion distances in the growth front and thus the height of the induced stress gradients. Since interface reactions are usually associated with volume changes, growth rates of reaction rims and zones in coronas are not only controlled by the diffusive mobility of the components but also by the volume restraints on the interface reactions. Received: 19 July 2002 / Accepted: 14 February 2003     

Experimentally derived thermochemical data for pargasite and reinvestigation of its stability with quartz in the system Na2O–CaO–>MgO–Al2O3–SiO2–H2O

 The stability of pargasite in the presence of excess quartz has been determined in the range of 0.5–6.0 kbar and 500–950 °C in the system Na₂O– CaO–MgO–Al₂O₃–SiO₂–H₂O, using synthetic minerals. The experimental results from this study indicate the presence of two distinct mineral assemblage regions: (1) a high temperature supersolidus region containing tremolitic amphibole+melt+quartz; (b) a low temperature subsolidus region consisting of Al-rich amphibole+plagioclase+enstatite+quartz. Compositional reversals have been determined for the following three equilibria: (a) 2 pargasite+9 quartz=tremolite+4 plagioclase (An₅₀)+1.5 enstatite+H₂O, (b) 2 pargasite+10 quartz=tremolite+4 plagioclase (An₅₀)+talc, and (c) pargasite+diopside+5 quartz=tremolite+2 plagioclase (An₅₀). These experiments indicate a continuous change of amphibole composition from pargasite to tremolite with increasing temperature, and an opposite effect with increasing pressure. The third equilibria is used to constrain a site-mixing model for the pargasitic amphiboles, which favor a single-coupled Na^A-Al^T1 site mixing. The thermochemical data for pargasite estimated from the reversal data of the three equilibrium reactions is estimated as for ΔG ⁰ _f ,Pg=−12022.11±5.2 kJ mole^-1, and S ⁰ _Pg=591.7 ±7.9 JK^-1 mole^-1. Received: 31 July 1995/Accepted: 3 June 1996     

Epithermal mineralization and ore controls of the Shasta Au-Ag deposit, Toodoggone District, British Columbia, Canada

The Shasta gold-silver deposit, British Columbia, Canada, is an adularia-sericite-type epithermal deposit in which deposition of precious metals coincided with the transition of quartz- to calcite-dominant gangue. Mineralization is associated with stockwork-breccia zones in potassically altered dacitic lapilli tuffs and flows, and consists of pyrite, sphalerite, chalcopyrite, galena, acanthite, electrum and native silver. Pre- and post-ore veins consist solely of quartz and calcite, respectively. Fluid inclusion microthermometry indicates that ore minerals were deposited between 280 ° and 225 °C, from a relatively dilute hydrothermal fluid (˜1.5 wt.% NaCl equivalent). Abundant vapor-rich inclusions in ore-stage calcite are consistent with boiling. Oxygen and hydrogen isotopic data (δ¹⁸O_fluid = −1.5 to −4.1‰; δD_fluid = −148 to −171‰) suggest that the fluid had a meteoric origin, but was ¹⁸O-enriched by interaction with volcanic wallrocks. Initial (˜280 °C) fluid pH and log f O₂ conditions are estimated at 5.3 to 6.0, and −32.5 to −33 bar, respectively; during ore deposition, the fluid became more alkaline and oxidizing. Ore deposition at Shasta is attributed to localization of meteoric hydrothermal fluids by extensional faults; mineralization was controlled by boiling in response to hydraulic brecciation. Calcite and base metal sulfides precipitated due to the increase in pH that accompanied boiling, and the associated decrease in H₂S concentration led to precipitation of gold and silver. Received: 23 February 1995 / Accepted: 16 April 1996     

Electric conductivity of Fe2SiO4–Fe3O4 spinel solid solutions

 The spinel solid solution was found to exist in the whole range between Fe₃O₄ and γ-Fe₂SiO₄ at over 10 GPa. The resistivity of Fe_{3− x} Si _x O₄ (0.0<x<0.288) was measured in the temperature range of 80∼300 K by the AC impedance method. Electron hopping between Fe³⁺ and Fe²⁺ in the octahedral site of iron-rich phases gives a large electric conductivity at room temperature. The activation energy of the electron hopping becomes larger with increasing γ-Fe₂SiO₄ component. A nonlinear change in electric conductivity is not simply caused by the statistical probability of Fe³⁺–Fe²⁺ electron hopping with increasing the total Si content. This is probably because a large number of Si⁴⁺ ions occupies the octahedral site and the adjacent Fe²⁺ keeping the local electric neutrality around Si⁴⁺ makes a cluster, which generates a local deformation by Si substitution. The temperature dependence of the conductivity of solid solutions indicates the Verwey transition temperature, which decreases from 124(±2) K at x=0 (Fe₃O₄) to 102(±5) K at x=0.288, and the electric conductivity gap at the transition temperature decreases with Si⁴⁺ substitution. Received: 15 March 2000 / Accepted: 4 September 2000