Uranoan thorite crystals have been found occurring as a sparse constituent in lithophysae in 6.1 to 6.8 Ma alkali rhyolite flows at Thomas Mountain, Utah, USA. The crystals are associated with sandidine, quartz, topaz, hematite, magnetite, and calcite; they are leek to dark grass green, transparent, well-formed, euhedral prisms, showing development of forms {100}, {101}, and {111}. The mineral is both optically isotropic, with a refractive index of 1.86(1), and X-ray amorphous, indicating its metamict state. Electron microprobe analysis yields: SiO2 17.3, ThO2 56.8, UO2 25.4, total 99.5%, and a structural formula of (Th0.72U0.31)Σ1.03Si0.97O4.

This appears to be the first reported occurrence of thorite in volcanic rocks of rhyolitic composition, and may account for part or all of the Th reported in alkali rhyolites and so-called ‘topaz-rhyolites’ of the western USA.

Concentration, conductivity, temperature, and flow logs from sixteen brine-filled shafts in northern Germany have shown that the brines in all former potash salt mines exhibit a very sharp stratification into lower Mg-rich brine, an upper layer of Na-rich brine, and groundwater at the top. Laboratory experiments have shown that, at the MgCl2-brine/NaCl-brine boundary, both solutions become oversaturated with regard to NaCl, due to diffusion processes. NaCl therefore crystallizes from the solutions and forms a salt plug in the boundary region, which considerably reduces further diffusion. It is concluded that the observed effects would also take place in shafts. The backfilling material helps to nucleate the halite crystals and provides a structure on which they might be supported. The results of these experiments show that the density boundaries in the brine bodies act as barriers against transport of matter while the formation of a halite plug growing independently at the MgCl2/NaCl-brine interface acts as an additional barrier.

A combination of hydrogen and oxygen isotope analyses and fluid inclusion studies has defined the composition of fluids involved in the metamorphism of Lower Palaeozoic rocks in the English Lake District. Three fluid fields have been defined from secondary phases: 1, syn-burial metamorphic D-enriched fluids from epidote and chlorite at a temperature between 250 and 350°C; D-depleted fluid measured from groundmass and quartz inclusions; 3, a mixed magmatic-meteoric fluid with an intermediate H-isotopic composition estimated from W/R granite data and calculated from illite.

The strongest lines in the X-ray powder diffraction pattern of type material of glaucocerinite from Laurion (Greece), indexed on a hexagonal pseudocell, are 10.9 (100) (003), 5.45 (90) (006), 3.63 (80) (009), 2.62 (60) (012), 2.46 (60) (015), 2.231 (50) (018), and 1.981 Å (50) (0.1.11). The pseudocell parameters are a 3.0700(8), c 32.65(1) Å. Chemical analysis of topotype material yields the formula [(Zn,Cu)5Al3(OH)16] [(SO4)1.5·9H2O] based on a pyroaurite-like structure. The pseudocell parameters for this sample are a 3.057(3), c 32.52(5) Å. Optical data are 2Vα ⋍ 60°, α 1.540, β 1.554, γ 1.562; D(meas.) = 2.4±0.1 g/cm3, D(calc.) = 2.33 g/cm3. So-called ‘woodwardite’ from Caernarvonshire, Wales, is identified as the Cuanalogue of glaucocerinite. An ‘11 Å mineral’ occurring together with carrboydite in Western Australia is shown to be the Ni-analogue of glaucocerinite. Alleged cotype glaucocerinite from Laurion is related to woodwardite and has the formula [(Zn,Cu)2Al(OH)6][(SO4)0.5 · 3H2O]. This is a cation-ordered pyroaurite-type structure with hexagonal cell parameters a 5.306(2), c 26.77(2) Å. The strongest X-ray powder lines occur at 8.9 (100) (003), 4.47 (90) (006), 2.55 (60) (113), and 2.28 Å (50) (116).

Junitoite, CaZn2Si2O7·H2O, is orthorhombic, space group Area2, with a = 12.510, b = 6.318, c = 8.561 Å, Z = 4. The structure, determined on the basis of three-dimensional Mo-Kα intensity data for 745 reflections refined to R = 0.10. The structure consists of ZnO4 tetrahedral chains along b joined by Si2O4 groups along a and c to form a three-dimensional network. Ca occurs in distorted CaO5(H2O) octahedra. The structure shows similarities to hemimorphite and Ca-Zn silicates but represents a unique tetrahedral framework.

In southern Kerala, India, chrysoberyl occurs in granitic pegmatites in association with quartz in alkali feldspar and is thought to crystallize earlier than beryl and sillimanite. The pegmatites are thought to have derived from the residual melts of granitic liquids formed by partial melting of the khondalites. In the absence of pyrometasomatic, desilication or aluminium-contamination processes, the genesis of chrysoberyl is explained by the CO2 activity in residual melts. This model is at variance with the known concepts and may also explain the genesis of chrysoberyl in Sri Lanka where it is still controversial.

The Cerro Prieto geothermal system provides a unique opportunity for the detailed study of calc-silicate mineral transitions between the diagenetic clay-carbonate and greenschist facies within the terrigenous sediments of the Colorado River delta. In this system, progressive devolatization reactions within carbonate-cemented, quartzofeldspathic sediment have produced a distinct hydrothermal mineral zonation at temperatures between 200–370°C and fluid pressures below 0.3 kbar. Descriptive and compositional data are presented for these minerals which include wairakite, epidote, prehnite, actinolite, clinopyroxene, garnet, sphene, biotite, microcline, and calcite. Partitioning of octahedral Fe, Mg, and Al between coexisting authigenic silicates is comparable with data from higher temperature metamorphic rocks and demonstrates an approach to local equilibrium within this system. Calculated fugacities of oxygen at temperatures above 300°C are (with rare exception) more reducing than that defined by the quartz-fayalite-magnetite buffer, a result consistent with the scarcity of hematite and grandite and the ubiquitous presence of organic material in Cerro Prieto sandstones.

Studies of the U decay series (238U-234U-230Th) have been carried out on samples from unaltered bedrock and highly altered fracture/crush zones from drillcore Km3 (Kamlunge test-site). The fracture zones are characterized by abundant iron oxide coatings (hematite and hydroxy iron oxides) resulting from the passage of hydrothermal solutions coeval with the Lina granite intrusion. Enrichments of U and Th, thought to be due to co-precipitation (or preferential sorption) processes together with the iron-oxides, are also present.

The isotopic results show that out of a total of twelve rock samples measured, six indicate isotopic disequilibrium mostly due to unequal depletions of 234U and 238U; one near-surface sample indicated some minor assimilation of U. The major fracture zones generally indicate removal of total U. This has resulted from interaction with groundwaters which are still marginally oxidizing, even at depths of 375 m.

Isotopic disequilibrium has occurred within recent geological times, i.e. during the last 0.5 Ma as imposed by the half-lives of 234U and 230Th. In terms of radioactive disposal considerations, the results are important in that: (1) the investigated bedrock environment (100–500 m) is generally reducing; however (2) there is some evidence to indicate that rock/water interactions, leading to the removal of total U, have resulted from the presence of less reducing groundwaters within those large-scale fracture/crush zones which intersect the bedrock surface.

Electron probe microanalyses of zoisites from high-grade metamorphic rocks in Galicia, NW Spain have been obtained. The elements Na, Mg, P, K, Ti, and Mn were not detected above the 0.1 wt. % level. Assuming all Fe is present as Fe3+, a clear relation is obtained between the Fe content and the optic axial angle. Zoisite with 1.6 wt. % Fe2O3 proves to be uniaxial at 589 nm; uniaxiality in blue light (470 nm) lies at 1.5 wt. % Fe2O3. A change of the optic sign, from positive to negative, is obtained at 2.9 wt. % Fe2O3. The presence of minor elements greatly affects this relation, as is indicated by analyses of sector-zoned Sr-bearing zoisites of a muscovite-zoisite pegmatite from the same region. Under retrograde conditions Fe-rich α-zoisite reacts to form less Fe-rich α-zoisite or β-zoisite and clinozoisite.

Clinopyroxene phenocrysts and groundmass crystals are relict phases in altered basalt and basaltic andesite lavas, and arenites of the Cudgegong Volcanics and Toolamanang Volcanics, Cudgegong-Mudgee district, New South Wales. Petrography, field relationships and clinopyroxene compositions indicate that basaltic blocks in the latter unit are reworked from the Cudgegong Volcanics. Clinopyroxene phenocrysts show a restricted compositional range and minor Feenrichment from core to rim, features considered indicative of a calc-alkaline parent magma. It is proposed that the Cudgegong Volcanics crystallized under hydrous conditions, at least in the later stages, with rising fO2 resulting in a Fe-Ti oxide crystallizing as a primary phase. The clinopyroxenes are considered to have crystallized at moderate (5–6 kbar) and falling pressures and at minimum temperatures in the range 900 to 1000°C. Coupled substitutions affecting the “other” components in the clinopyroxene structural formula indicate that the ivAl-viFe3+, ivAl-viAl and ivAl-viTi4+ couples are important. The Sofala Volcanics, south of the study area, and the Cudgegong Volcanics are similar in age, petrography and stratigraphic position, and contain relict clinopyroxenes which are chemically similar. This suggests that the units are laterally equivalent and adds further evidence to the proposal that an oceanic island arc system was active in central western New South Wales during the Late Ordovician.

Hey's observation of reduction of ferric ion bound to 1,10-phenanthroline in water is explained in terms of the analogy between quaternization of the ligand and its coordination by iron(III).

Two metamorphic alteration styles have been observed in basic lavas and volcaniclastic rocks of the Builth Volcanic Series of Ordovician age exposed at Llanelwedd Quarry, in the Builth lnlier, Wales. The first alteration style is characterized by the development of a mineral assemblage comprising albite+chlorite+ sphene+ pumpellyite ± prehnite ± calcite ± white mica, although original textures are largely preserved. This alteration pattern corresponds with that developed in volcanic and volcaniclastic rocks elsewhere in Wales, and which is attributed to the effects of burial. The second alteration style is characterized by the development of metadomains dominated by pumpellyite or, more rarely, prehnite. In the metadomains no original textures are seen in hand specimen. This alteration pattern has, so far, not been observed elsewhere in Wales, and it is here suggested that it might result from a submarine hydrothermal circulation system.

The first results of isotopic investigations as a part of the hydrogeological study of northern Switzerland are presented. This study is part of the global geological research project of the NAGRA (National Co-operative for the Storage of Radioactive Waste) which is intended to provide the scientific knowledge required for the assessment of the feasibility of safe disposal of highly radioactive waste in the geological formations of the area. The aim of the hydrogeological research programme is to assess the natural conditions in the sedimentary sequence and the underlying granite basement, by regional investigation of hydraulic parameters, isotopic composition, and hydrogeochemistry at all existing wells (boreholes and natural thermal springs) and in 11 to 12 deep-drilled boreholes (to final depth of 1500–2500 m).

Qandilite, a new species of the spinel group, has been found in a forsterite-rich rock in contact with a kaersutite-rich banded diorite from the Qala-Dizeh region, NE Iraq. Chemical analysis yielded MgO 29.62, FeO 10.32, MnO 0.76, Fe2O3 28.27, Al2O3 4.83, TiO2 26.41, SiO2 0.02, sum 100.23 wt. %. This analysis calculates to [(Mg1.20Ti0.60)][Mg0.12Mn0.02)(Al0.17)]O4 with a composition of Mg2TiO4 63.8, MgFe2O4 12.8, FeFe2O4 23.4 mole %. Qandilite is cubic with a = 8.4033±0014 Å; cell volume 593.40 Å3 and space group Fd3m; Z = 8. The seven strongest lines in the X-ray diffraction pattern are (d,I,hkl): 2.971, 30, (220); 2.53, 100, (311); 2.101, 45, (400); 1.617, 50, (333, 511); 1.486, 60, (440); 1.0938, 30, (553, 731); 0.9704, 25, (555, 751). The colour is black, lustre metallic, streak black, fracture even and the cleavage perfect on (111). It is opaque, strongly magnetic, Dcalc = 4.04, Dmeas = 4.03, and VHN100 = 960–1045 kg/mm2, with H-7. The reflection colour is grey with a pinkish tint; it is isotopic with no internal reflections. Reflectance measurement data in air and oil in the range (400–700 nm) are given. Colour values for illuminant C in air and oil in terms of CIE colour space are: x = 0.307, 0.307; y = 0.311, 0.310; Y% = 13.10, 3.0; λd = 465, 460; and Pe% = 2.0, 2.2. Calculated data for the absorption coefficients (k) and refractive indices (n) in the range 400–700 nm are also presented.

Pseudomesolite from Carlton Peak, described by Winchell (1900), is shown to be mesolite by means of chemical and X-ray data. A proposal to this effect has been accepted by the International Mineralogical Association's Commission on New Minerals and Mineral Names. Electron microprobe analysis revealed variations in the composition of pseudomesolite and showed the presence of faroelite. The X-ray powder diffraction pattern is similar to that of mesolite. Single-crystal Weissenberg photographs showed a twinning intergrowth which is explained by a 90° rotation of 50% of the unit cells about the c-axis, so that the a- and b-axes of rotated cells coincide with the b- and a-axes respectively of the unrotated cells. This twinning can not be detected optically. Mesolite has recently been proved to be orthorhombic, contrary to the long-held view that it is monoclinic.

Pseudomesolite from Oregon is also shown to be mesolite by single crystal Weissenberg photographs. A wet chemical analysis shows this material to be extremely silica-rich.

Heat flow in SW England is well above average for the UK as a whole, but northwards towards Bath and Bristol the values decrease rapidly. However, hot springs occur both in the Bath-Bristol area and in mines in Cornwall. The development of hydrothermal circulation systems is thus not controlled entirely by geothermal gradient: the presence of a suitable fracture permeability is the main requirement. The thermal ‘head’ produced, which nevertheless depends upon the temperature and volume of water in the system, theoretically can exceed local topographic heads even in areas of low geothermal gradient.

Thermal groundwaters usually carry above average quantities of radioelements in solution because of the long residence times involved. 222Rn values are often particularly high. High concentrations of 222Rn in surface waters arise from the discharge of groundwater. The results of a survey of 222Rn in streams in SW England have established areas of high values which are interpreted as rising limbs of convection cells with dimensions in the order of 5–10 km.

In SE Devon γ-ray spectrometry of soils shows two E.-W. belts of high activity. The northern is coincident with the faulted southern margin of the Crediton Trough, while the southern is coincident with the westerly extension of the Abbotsbury fault system. Groundwater movement along deep-seated fracture systems is considered to be the explanation of these features. The horizontal scale of the area involved suggests that a thermal rather than local topographic head is the driving force. Groundwater circulation within fractures, driven by a thermal head, may therefore occur even in areas of low geothermal gradient and should be considered when selecting waste disposal sites.

Calcite cements from the Lower Cretaceous Avalon zone of the Hibernia field are, in places, extensively recrystallized, which complicates interpretation of the chemical and isotopic data. The oxygen isotopic data are widely scattered with δ18O ranging between +1.6 and −9.2 for calcite and siderite. Siderite has lower δ13C values (−6.6 to −13.2) than calcite +12.4 to −9.8. Typical trace element contents determined by ICP on acid-leached samples, range from 270 to 2100 ppm Sr and 180 to 2200 ppm Zn in calcite.

The trace element data indicate that some of the calcite has been precipitated from, or recrystallized by meteoric water. The trace elements show trends related to variations in δ18O in such a way as to imply that not all the spread to low δ18O values can be attributed to meteoric water influence alone. The data are not well enough constrained to calculate meaningful temperatures, but the range of °18O values probably represents an elevated range of temperatures of precipitation or recrystallization.

Microprobe analyses show that non-recrystallized fossils have a composition distinctly different from veins, cements, and recrystallized fossils, all of which are similar. The compositions of calcite cements are highly variable, with FeO (for example) ranging from 0.15 to 4.39 wt. %, but show no consistent patterns of zonation. Fossil fragments which show no textural evidence of recrystallization have low FeO contents (0.2 wt. %). Meteoric water, believed to be responsible for at least some of the cementation and recrystallization observed, probably entered the Avalon during and after formation of the mid-Cretaceous unconformity.