The Cu-Se system

Phase-relations in the Cu-Se system were determined by evacuated silica-tube experiments. The phase diagram up to 1100° C was obtained from the results of differential thermal analyses of pure compounds and of their mixtures. The phases in the system are: Cu₂Se — undergoes a polymorphic transformation at 150° C. The symmetry of the low temperature form is not yet known. The high form is cubic with a fluorite-type structure. Cu_2–xSe — cubic, with x variable in a very narrow range, at room temperature. Cu₃Se₂ — tetragonal, breaks down to Cu_2–xSe and CuSe at 150° C. CuSe — hexagonal below 60° C and, presumably, orthorhombic at higher temperature, melts incongruently at 387° C to Cu_2–xSe and a Se-rich liquid. CuSe₂ — orthorhombic, melts incongruently at 347° C to CuSe and a Se-rich liquid. The presence of an eutectic at 523° C was inferred from differential thermal heating and cooling curves.

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Zusammenfassung Die Phasenbeziehungen im Cu-Se System wurden durch Versuche mit Hilfe evakuierter Quarzampullen bestimmt. Bis zu 1100° C wurden die Ergebnisse der Differential-Thermoanalyse verwendet. Die Phasen im System sind: Cu₂Se: wandelt sich bei 150° C polymorph um. Die Symmetrie der Tieftemperaturform ist noch nicht bekannt, während die Hochtemperaturform kubisch ist (Flusspatstruktur). Cu_2–xSe (kubisch) hat bei Raumtemperatur einen sehr kleinen x-Wert. Cu₃Se₂ (tetragonal) spaltet sich bei 150° C zu Cu_2–xSe und CuSe. CuSe (hexagonal) ist unterhalb 60° C vermutlich rhombisch und bei höherer Temperatur (387° C) zersetzt es sich inkongruent zu Cu_2–xSe und einer Se-reichen Schmelze. CuSe₂ (rhombisch) zersetzt sich bei 347° C inkongruent zu CuSe und einer Se-reichen Schmelze. Die Anwesenheit eines Eutektikum bei 523° C wird aufgrund von DTA-Analysen angenommen.

     

Thermal expansion and glass transition temperatures of synthetic glasses of plagioclase-like compositions

The glass transition temperatures and the thermal expansions both below and above the glass transition temperature region of synthetic glasses of compositions close to those of plagioclases have been determined. The linear thermal expansion coefficient of the rigid glasses decreases on average from 7.4×10^–6/dgC for albite glass to 4.9×10^–6/dgC for glass close to anorthite composition. The glass transition temperature of the glasses initially decreases from 763° C for albite glass to 752°C for An_9.7 glass and then increases nearly linearly with further increasing anorthite content to 813° C for glass close to anorthite composition.—Measurements made for comparison on a glass prepared from Madagascar orthoclase yielded a linear thermal expansion coefficient of 6.1×10^–6/dgC and a glass transition temperature of 905° C.The variations in thermal expansion and glass transition temperature of the feldspar glasses with composition are discussed in terms of structural changes which are assumed to be associated with cation replacement.     

The role of synmetamorphic igneous rocks in the metamorphism and partial melting of metasediments,Northwest Adirondacks

Field and petrologic studies along the Adirondack Lowlands — Highlands boundary near Harrisville, NY, indicate that heat from the synmetamorphic intrusion of the Diana syenite complex (intrusion temperature of 1,050° C) played a major role in the local metamorphic thermal regime and was responsible for extensive partial melting of adjacent metasedimentary units (Major Paragneiss of Engel and Engel). Metamorphic temperatures inferred from two — feldspar and spinel — quartz assemblages decrease from 850–950° C along the Diana — metasediment contact to 650–700° C, 2–3 km away from the contact. Metamorphic pressures are 7±0.5 kb as determined from coexisting plagioclase — garnet — sillimanite — quartz, kyanite — sillimanite, and garnet — rutile — ilmenite — sillimanite — quartz (GRAIL). In the paragneiss, migmatites consisting of quartz — microcline perthite — sodic plagioclase leucosomes are generally concordant with the melanosome consisting of biotite — sillimanite — garnet — spinel — plagioclase ±corundum±cordierite. Qualitatively the amount of partial melt and occurrences of corundum-bearing assemblages decrease away from the Diana contact. Activity of H₂O inferred from coexisting biotite — sillimanite — quartz — garnet — K-feldspar ranges from 0.01 to 0.17 and is five to ten times lower in corundum-bearing rocks.Melting proceeded via vapor-absent reactions involving biotite in response to localized heating by synmetamorphic intrusion of magma. This unusually preserved, synmetamorphic contact aureole in a regional granulite terrane supports the concept that granulites owe their origin to magma intrusion and/or the ponding of magmas at the base of the crust.     

The distribution of snow in Israel

The area researched is characterized by changes in the weather according to fluctuations in the world pressure belts throughout the year. The temperature climate in this region is typified in winter by changes in the pressure system from cyclonic to anti-cyclonic conditions in spells of about 5 days.When Israel is under the influence of a low pressure system, and the 500 mb surfaces are approximately 250 m lower than average, the temperatures along the vertical cross-sections are 6° – 8° C lower than average on rainy days, then snow may be expected in various sections of the country.This paper investigated the 35 years period from 1938/9 to 1971/2, concentrating on two mountain stations — Jerusalem in the centre of the country and Mt. Kena'an in the north —because of the high snow incidence and its greater regularity than other stations.The conclusions are as follows: The maximum number of days of snow (between 2/3 and 3/4 of the annual total) is noted at all stations during January and February, although there are also years in which there was snow but not during those months. Regional devision of the snowy days indicates that the number increases with altitude, and decreases from north to south.Snowfall in regions which have lower incidence is less stable and given to greater fluctuations. There was no indication of periodity of the number of days of snow per season, nor did it appear that a very snowy year followed a dry one.Investigation of the lenght of the snowy and the number of days of snowfall does not indicate any connection between them, and there may well be a long season with few days of snow, or a short one with relatively many snowy days.Comparison between the shorter period of readings — from 1938/9 till 1971/2 — and the longer one — from 1860/1 till 1971/2 (111 years) — at the Jerusalem station shows the same trends, which reinforce the conclusions presented above.     

Dehydration-melting of amphibolite at 10 kbar: the effects of temperature and time

We have simulated the dehydration-melting of a natural, low-K, calcic amphibolite (67.4% hornblende, 32.5% anorthite) in piston-cylinder experiments at 10 kbar and 750–1000°C, for 1–9 days. The solidus temperature is lower than 750°C; garnet appears at 850°C. The overall reaction is: Hb+PL+Cpx+Al-Hb+Ca-Hb+Ga+Opx. Three stages of reaction are: (1) melting dominated by the growth of clinopyroxene and garnet, with little change in composition of liquid or garnet, (2) a reversal of this reaction between 875°C and 900°C, with decreases in the amounts of liquid and garnet, and (3) a large increase in liquid along with the loss of hornblende and decrease of plagioclase while clinopyroxene and garnet increase. Garnet is enriched in pyrope and zoned from Fe-cores to Mg-edges (range 3 mol % pyrope); liquid composition is enriched first in An (to 950°C) and then in Ab. The liquids are more calcic and aluminous than natural tonalites, which is attributed to the plagioclase composition (An₉₀). The formation of peraluminous liquid from the metaluminous amphibolite is caused by anorthite — not H₂O-saturated conditions. The results are consistent with an amphibolite phase diagram with relatively high solidus temperatures in the garnet-absent field (900–1000°C), but with a solidus backbend at 7–9 kbar, coincident with the garnet-in boundary. Hornblende breakdown due to garnet formation in a closed system must make H₂O available for H₂O-undersaturated melting right down to the H₂O-saturated solidus, below 700°C, which defines a large low-temperature PT area where hydrous granitoid melts can be generated with residual garnet and hornblende.     

Fluorine-hydroxyl exchange in apatite and biotite: A potential igneous geothermometer

The free energy data for the simple fluorides, chlorides and hydroxides have been used to predict the distribution of these anions in hydrous minerals. The calculated partition of fluorine in phlogopite agrees well with published results; the distribution of fluorine and hydroxyl between apatite and phlogopite is temperature dependent and has been calculated. The temperatures deduced from analyses of natural apatite-biotite pairs frequently show discrepancies as compared with independent temperature estimates; these probably arise from late-stage exchange of the fluorine in phlogopite with an aqueous fluid, for which independent evidence is available.The fugacity of phosphorus in equilibrium with apatite, a ubiquitous hydrous mineral, has been calculated for various mineral assemblages. The estimates, which are subject to considerable error, are lower for basanites and alkali-basalts than for tholeiites and range from approximately 10^–14 at 1000° C to 10^–16 bars at 750° C for fayalitic rhyolites.     

High temperature alteration of Abyssal ultramafics from the Islas Orcadas Fracture Zone,South Atlantic

Ultramafic rocks dredged from the Islas Orcadas Fracture Zone, along the SW Indian Ocean Ridge (6° E and 54° S), show evidence of progressive hydration beginning at temperatures greater than 600° C (and perhaps as high as 900° C) and continuing to less than 50° C. There are two principal types of alteration present in the ultramafic rocks, both of which are the result of hydration reactions. The first type of alteration involves hydration of original clinopyroxene, orthopyroxene and olivine to amphibole, talc, secondary olivine, and serpentine. The second is a vein type of alteration and results in the formation of veins of amphibole, chlorite, talc and serpentine. — The alteration appears to be episodic. The sequence of events suggested by the petrography is: 1) clinopyroxene altering to amphibole; 2) orthopyroxene altering to talc, or talc + olivine; 3) supersolvus hornblende veining; 4) coexisting actinolite + hornblende veining; 5) chlorite, chlorite + actinolite, or chlorite + secondary clinopyroxene veining; 6) talc veining; 7) serpentine veining; and 8) pervasive serpentinization. — The alteration fluid is most likely seawater. It is suggested that the high temperature alterations may reflect seawater circulation into the upper mantle.     

Garnet-cordierite-biotite equilibria in the Steinach aureole,Bavaria

Three garnet-biotite pairs and eleven garnet-cordierite-biotite triplets from the Steinach aureole (Oberpfalz, North-East Bavaria) were analyzed using an electron probe microanalyzer.The regional metamorphic muscovite-biotite schists contain garnets strongly zoned with Mn-Ca-rich centers and Fe-rich edges, the average composition being almandine 67 — spessartine 4 — pyrope 4 — grossular (+andradite) 25.The first contact garnet that is formed in mica schists of the outermost part of the aureole is small, virtually unzoned, and has an average composition of almandine 52 — spessartine 37 — pyrope 8 — grossular (+andradite) 3. With increasing metamorphic grade, there is a consistent trend to form garnets richer in Fe ending up with a composition almandine 84.5 — spessartine 5.5 — pyrope 7.5 — grossular (+andradite) 2.5. This trend is accompanied by a general increase in grain size and modal amount of garnet. Associated cordierites and biotites also become richer in Fe with increasing grade. While the garnets in the highest grade sillimanite hornfelses are poorly zoned, the transitional andalusite-sillimanite hornfelses contain garnets with distinct but variable zonation profiles.These facts can possibly be explained by the time-temperature relationships in the thermal aureole. In a phase diagram such as the Al-Fe-Mg-Mn tetrahedron, the limiting mineral compositions of a four-phase volume or a three-phase triangle are fixed by T and P (the latter remaining effectively constant within a thermal aureole). Thus, in garnet-cordierite-biotite assemblages, garnet zonation should be controlled by temperature variation rather than by a non-equilibrium depletion process. Taking into account the experimental data of Dahl (1968), a zoned garnet from a transitional andalusite-sillimanite hornfels would reflect a temperature increase of about 40° C during its growth. A hypothetical P-X diagram is proposed to show semi-quantitatively the compositional variation of garnet-cordierite pairs with varying pressures (T constant).     

Experimental crystal growth in glass inclusions: the possibilities and limits of the method

Glass inclusions trapped in bytownite phenocrysts (from the Ardoukoba eruption, Djibouti Republic, 7 November 1978) are used as an experimental environment to follow the evolution of crystallization and residual liquids in a magma with tholeiitic affinities. The results are compared with those obtained from abyssal tholeiites by Walker et al. (1979). In near equilibrium crystallization conditions, simultaneous crystallization of olivine and pyroxene is obtained in the enclosed silicate liquid as well as plagioclase as overgrowths on the cavity walls. Oxides only appear at lower temperatures. The olivine is homogeneous and rather rare (5% in weight). It forms at a temperature between 1,186° C±3(Fo85) and 1,126° C(Fo66). The distribution coefficient of Mg between the liquid and the olivine varies regularly with the temperature until titanomagnetite appears. The augite is much more abundant (>20% in weight of the original trapped melt) and is characterized by a composition that varies from the centre to the edges of the crystals Wo 43.5–36.2, En 43.8-41.7, Fs 12.7–22.1. Composition shows an unsatisfactory correlation with temperature and, at most, an Fs enrichment may be noted with temperature decrease. The composition of the plagioclase deposited on the cavity walls varies linearly with temperature from An 73.3 at 1,186° C to An 56.5 at 1,135° C in the case of contemporaneous crystallization of Pl, Cpx, Ol and Ox. If experiments are carried out by undercooling (as much as 150° C) in relation to crystallization of the ferromagnesian minerals, the composition of the plagioclase changes from An 78.8 at 1,160° C to An 52.8 at 1,025° C. In the case of the Pl, Ol, Cpx and +OX crystallization, the included liquids evolve from tholeiitic basalts to ferrobasalts in the same way as the lavas studied in the Asal rift (Demange et al. 1980). The advantages and limitations of the method are discussed.     

Geology and geothermometry of vein-type W-Sn deposits at Pennaichaung and Yetkanzintaung Prospects,Tavoy Township,Tennasserim Division,southern Burma

The Pennaichaung and Yetkanzintaung W-Sn Prospects are located in Tavoy Township, Tennasserim Division, southern Burma. The W-Sn mineralization at the Pennaichaung is closely related with a small, satellitic granitoid pluton of presumably Late Mesozoic age, which intruded the metaclastic rocks of Mergui Group (mostly Carboniferous). The mineralized quartz veins at the Pennaichaung penetrated the granitoid-metasedimentary rocks contact. In contrary to the Pennaichaung deposit, the W-Sn veins at the Yetkanzintaung are exclusively in the metasedimentary rocks of slates and quartzites of Margui Group. Mineralized quartz veins in the Pennaichaung area trend NNE-SSW, NW-SE and NE-SW with a maximum thickness of 30 cm, but only quartz veins trending NNE-SSW are found to be productive and contained economically workable wolframite and cassiterite. Majority of the mineralized quartz veins in the Yetkanzintaung area trend approximately N-S with easterly dip of 50°–70°. The thickness of the ore veins in the Yetkanzintaung area are thinner than those of the Pennaichaung and range from 1 cm to 20 cm with an average width of 5 cm. Fluid inclusion studies of the quartz from the ore veins cutting the granitoid in the Pennaichaung area have yielded a filling temperature range of 170°–270°C with a maximum mode of 220°C, while quartz crystals from the ore veins in the nearby metasedimentary rocks gave a filling temperature range of 140°–220°C with a maximum mode of 160°C. Hence, the Pennaichaung deposit was thought to have emplaced under a filling temperature range of 140°–270°C. A similar low filling temperature range was recorded for the Yetkanzintaung deposit. Quartz from the Yetkanzintaung ore veins have yielded filling temperatures of 200°–240°C, whereas the fluorites associated with the mineralized quartz veins gave a temperature range of 140°–160°C. Limited freezing runs indicate a salinity of less than 5 NaCl equivalent weight percent for inclusions in quartz from both orebodies. No fluid inclusion evidence of boiling of ore fluids nor presence of liquid CO₂ was observed in this study. Thus, the ore fluids responsible for the W-Sn mineralization at the Pennaichaung and Yetkanzintaung areas were of low temperature, diluted, CO₂-deficient, NaCl brines.     

Order-disorder kinetics in orthopyroxenes of ophiolite origin

The kinetics of the Fe–Mg order-disorder reaction in four low-Fe orthopyroxenes (Fs_7–14) has been studied by use of Mössbauer spectroscopy, to determine cooling rates for the host rocks. The obtained Fe²⁺ distribution data were corrected for the thickness effect. The sample set was selected from rocks expected to have distinctly different cooling histories. Equilibrium data for the exchange reaction were determined for the temperature range 600–800°C, and kinetic data at 650°C. The results indicate that the degree of ordering in low-Fe orthopyroxene is substantially lower than estimated by thermodynamic models. The cooling rates obtained seem realistic for most samples, ranging from 19°C/min at 760°C for a boninite pillow lava to 2°C/million years at 267°C for a regionally metamorphosed olivinite. The errors in obtained cooling rates are estimated to be near one order of magnitude. An Fe³⁺ containing sample yields an unreasonably slow cooling rate which may be due to oxidation of Fe²⁺, occurring after the quenching point of the order-disorder reaction was reached.     

Phase relations and mineral assemblages in the Ag-Bi-Pb-S system

Phase relations within the Ag-Bi-S, Bi-Pb-S, and Ag-Pb-S systems have been determined in evacuated silica tube experiments. Integration of experimental data from these systems has permitted examination and extrapolation of phase relations within the Ag-Bi-Pb-S quaternary system. — In the Ag-Bi-S system liquid immiscibility fields exist in the metal-rich portion above 597±3°C and in the sulfur-rich portion above 563±3°C. Ternary phases present correspond to matildite (AgBiS₂) and pavonite (AgBi₃S₅). Throughout the temperature range 802±2°C to 343±2°C the assemblage argentite (Ag₂S) + bismuth-rich liquid is stable; below 343°C this assemblage is replaced by the assemblage silver + matildite. — Five ternary phases are stable on the PbS-Bi₂S₃ join above 400°C — phase II (18 mol-% Bi₂S₃), phase III (27 mol-% Bi₂S₃), cosalite (33.3 mol-% Bi₂S₃), phase IV (51 mol-% Bi₂S₃), and phase V (65 mol-% Bi₂S₃). Phase IV corresponds to the mineral galenobismutite and is stable below 750±3°C. Phases II, III, and V do not occur as minerals, but typical lamellar and myrmekitic textures commonly observed among the Pb-Bi sulfosalts and galena evidence their previous existence in ores. Phase II and III are stable from 829±6°C and 816±6°C, respectively, to below 200°C; Phase V, stable only between 730±5°C and 680±5°C in the pure Bi-Pb-S system is stabilized to 625±5°C by the presence of 2% Ag₂S. Experiments conducted with natural cosalites suggest that this phase is stable only below 425±25°C in the presence of vapor. — In the Ag-Pb-S system the silver-galena assemblage is stable below 784±2°C, whereas the argentite + galena mineral pair is stable below 605±5°C. — Solid solution between matildite and galena is complete above 215±15°C; below this temperature characteristic Widmanstätten structure-like textures are formed through exsolution. Schematic phase relations within the quaternary system are presented at 1050°C, at 400°C, and at low temperature.

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Zusammenfassung Die Phasenbeziehungen in den Systemen Ag-Bi-S, Bi-Pb-S und Ag-Pb-S wurden durch Versuche in evakuierten Quarzglasröhrchen bestimmt. Die Auswertung aller experimentellen Daten gestattete eine Extrapolation der Phasenbeziehungen im quaternären System Ag-Bi-Pb-S. — Im System Ag-Bi-S besteht ein Zwei-Schemlzenfeld im metallreichen Teil über 597±3°C und im schwefelreichen Teil über 563±3°C. Die ternären Phasen entsprechen den Mineralien Schapbachit (AgBiS₂) und Pavonit (AgBi₃S₅). Zwischen 802±2°C und 343±2°C ist die Paragenese Silberglanz (Ag₂S) + Bi-reiche Schmelze stabil; unterhalb 343°C wird sie jedoch ersetzt durch die Paragenese Silber + Schapbachit. — Fünf ternäre Phasen sind stabil im Schnitt PbS-Bi₂S₃ oberhalb von 400°C: Phase II (18 Mol-% Bi₂S₃), Phase III (27 Mol-% Bi₂S₃), Cosalite (33.3 Mol-% Bi₂S₃), Phase IV (51 Mol-% Bi₂S₃) und Phase V (65 Mol-% Bi₂S₃). Phase IV entspricht dem Mineral Galenobismutit und ist stabil unterhalb 750±3°C. Die Phasen II, III und V kommen zwar nicht in der Natur vor, jedoch weisen typische myrmekitische und lamellare Gefüge, die man häufig in Pb-Bi-Sulfosalzen und deren Verwachsungen mit Bleiglanz beobachtet, auf die ehemalige Existenz solcher Phasen in diesen Erzen hin. Die Phasen II und III sind stabil von 829±6°C bzw. 816±6°C bis unter 200°C. Die Phase V, die im reinen System Bi-Pb-S zwischen 730±5°C und 680±5°C auftritt, wird in Gegenwart von 2% Ag₂S stabilisiert bis herab zu 625±5°C. Versuche mit natürlichen Cosaliten lassen darauf schließen, daß diese Phase nur unterhalb 425±25°C in Gegenwart einer Gasphase stabil ist. — Im System Ag-Pb-S ist die Paragenese Silber-Bleiglanz unterhalb von 784±2°C stabil, die Paragenese Silberglanz-Bleiglanz dagegen unterhalb 605±5°C. — Die Mischkristallreihe von Schapbachit und Bleiglanz ist vollständig oberhalb 215±15°C; unterhalb dieser Temperatur entstehen charakteristische Entmischungsgefüge ähnlich den Widmannstättenschen Figuren. Für das quaternäre System werden schematische Phasenbeziehungen für 1050°C, 400°C und eine noch tiefere Temperatur gegeben.

     

Quantitative reconstruction of climate variability during the Eemian (Merkinė) and Weichselian (Nemunas) in Lithuania

Little is known concerning climate changes in the Eastern Baltic region during the last interglacial–glacial cycle and in particular, climate changes during the Weichselian. In this study, a quantitative reconstruction of the mean January and July temperature for the Medininkai-117 site in Lithuania is presented. The reconstruction is based on pollen and plant macrofossils from this site, which reveal that the vegetation was characteristic of many northern Europe sites during the Eemian and Early Weichselian. Gradual evolution of the vegetation suggests that relatively uniform climate conditions existed during the Eemian. Our reconstructions support the view of a relatively stable Eemian, with short cooling phases of low amplitude. A strong increase in temperature was apparent during the beginning of the interglacial and decrease during the transition to the Weichselian. Reconstructed July temperatures of the Eemian interglacial were approximately 2 °C higher than today (18.5 °C; today: 16.2 °C) and were similar to today for January (− 5.2 °C; today: − 5.1 °C). July temperatures during the Early Weichselian were only ~ 2°C lower than during the Eemian, whereas the January temperatures gradually decreased. Winter temperatures were relatively high (above − 10 °C) during the Early Weichselian.     

Variations of factors affecting rice productivity in Central Luzon,Philippines

Factors affecting rice productivity in Central Luzon, Philippines, among four classes of level, namely Class A — fully irrigated, Class B — partially irrigated, Class C — lowland rainfed, and Class D — upland rainfed, are examined in this study. An attempt is made to identify the ajor underlying dimensions of rice productivity and to ascertain the set of postulated factors that best determines variations associated with rice productivity. While principal-axes factor analysis is applied to isolate the underlying dimensions associated with rice productivity for 200 farms, stepwise multiple regression analysis is employed to determine which among the thirty-eight hypothesized variables have the strongest influence in accounting for variations associated with rice productivity in Central Luzon.The results showed that the economic and institutional factors accounted for most of the variations in rice productivity among the four classes of farms. Whereas the economic variables were concerned with the amount and manner in which economic inputs were used and with the amount of fixed asset in rice production, the institutional factors were focused mainly on membership in the government rice production program and the amount of loan available to farmer members.     

Mineralogical and colour changes of quartz sandstones by heat

Seven German and three Hungarian monumental sandstones have been tested in laboratory conditions to analyse the effect of heat. The studied quartz sandstones have a wide-range of cements and grain-sizes including silica-, carbonate-, clay- and ferrous mineral—cemented varieties of fine-, medium- to coarse-grained types. Cylindrical specimens were heated up to 150, 300, 450, 600, 750 and 900°C in an oven. The mineralogical and textural changes were recorded and compared by using microscopy, XRD, DTA-DTG and SEM. Colours and colour differences (a*, b*, L* values) were also measured and evaluated. Colour changes are related to mineral transformations. The most intense colour change is caused by the oxidation of iron-bearing minerals to hematite that takes place up to 900°C. When temperature increases the green glauconite becomes brownish while the chlorite changes to yellowish at first. The colour of burnt sandstone is not a direct indicator of burning temperature, since there are sandstones in which the burnt specimens are lighter and less reddish than the natural ones. Porosity increase is related to micro-cracking at grain boundaries (above 600°C) and within the grains (at and above 750°C) and mineral transformations. The clay mineral structure collapses at different temperatures (kaolinite up to 600°C, chlorite above 600°C) and leads to a slight increase in porosity. The most drastic change is observed in calcite cemented sandstones where the carbonate structure collapses at 750°C and CaO appears at 900°C. Subsequently it is transformed to portlandite due to absorption of water vapour from the air. This leads to the disintegration of sandstone at room temperature a few days after the heat shock.Special issue: Stone decay hazards     

Occurrence of pumpellyite in hydrothermally altered basalts from the Vema fracture zone (mid-Atlantic ridge)

Metabasalts with abundant pumpellyite have been dredged in the Vema fracture zone, Atlantic ocean, and contain prehnite+pumpellyite±epidote+chlorite+white mica. The prehnite — pumpellyite association in these rocks differs from the prehnite-epidote association for most of the prehnite — pumpellyite facies metabasalts from the ocean crust described previously. The occurrence of pumpellyite is discussed in terms of temperature conditions, and oxygen fugacity and the pumpellyiterich metabasalts are believed to be recrystallized by hydrothermal circulation of seawater at about 250° C under a very low pressure (<1 kb).The bulk composition of the rocks demonstrates a strong chemical modification during hydrothermal metamorphism, similar to what is observed under greenschist facies conditions, except for potassium which can be uptaken from seawater by the rocks.     

Chemical control of Al-solubility in orthopyroxene and its implications on pyroxene geothermometry

Two suites of spinel peridotites of the Westeifel/West Germany were found to have equilibrated in a narrow temperature interval each. Temperatures calculated from the CaO-solubility in orthopyroxene using experimental data of Lindsley and Dixon (1976) are 945° C to 980° C for the amphibole bearing Ia-suite and 1,150° C to 1,165° C for the Ib-suite. From the study of phase equilibria in both series it appears that Al-solubility in orthopyroxene is controlled by the composition of the coexisting spinel. Temperatures calculated from Al-solubility in orthopyroxene using an equation of Fujii (1976) derived from the univariant reaction en+spfo+Al-en in the MgO-Al₂O₃-SiO₂ system show a clear dependence on the FeCr₂O₄ component in the spinel phase, although ideal solution correction allowing for additional components was made. Temperatures obtained for the most chromite rich spinel — orthopyroxene pairs are 1,370° C and 1,240° C, respectively. These temperatures are by 220° C higher than those from Cr-poor pairs and those obtained from Ca solution in orthopyroxene.For practical purposes of geothermometry in spinel peridotites, an empirical equation allowing for the mole fraction of FeCr₂O₄ in spinel has been derived by a linear least squares fit to the orthopyroxene — spinel compositional data and temperatures calculated from the CaO-solubility of orthopyroxene in the present paper.     

Experimental exsolution textures in the system bornite-chalcopyrite: Genetic implications concerning natural ores

Textural interpretation of ore-mineral assemblages, such as bornite-chalcopyrite (bn-cpy) intergrowths, should be based on definite experimentation. Appropriate exsolution and coarsening experiments were performed using sealed, evacuated, silicaglass tubes; synthetic bn-cpy solid solutions were annealed between 100° and 350°C for times of 20 min to 10 weeks. Early-formed textures develop through nucleation and growth and depend on the initial degree of supersaturation and the metal diffusivities. Final textures, due to additional growth and coarsening, are very sensitive to temperature and may serve as geothermometers. Mutual boundary textures which form above 250°C can originate by: (1) simultaneous precipitation; (2) exsolution during slow cooling from above the solvus; and (3) metamorphism to temperatures above about 250°C. Widmanstätten textures are not compatible with slow cooling, but indicate: (1) low-temperature replacement of bn; or (2) exsolution of cpy lamellae from anomalous bn heated to around 200°–250°C during mild metamorphism.     

Reinvestigation of fayalite+anorthite=garnet

The reaction fayalite+anorthite=garnet (GAF) has been investigated in a piston-cylinder apparatus and in an internally heated gas apparatus. Piston-cylinder reversals were obtained at 900 °C (6.0–6.4 kbar), 950 °C (6.3–6.8 kbar), 1000 °C (6.6–7.1 kbar), and 1050 °C (7.0–7.3 kbar). Gas-apparatus experiments yielded a reversal at 7 kbar (993–1049 °C). Results are consistent with earlier experimental studies. Unless garnet Ca–Fe mixing is attended by an excess entropy of at least 2–3 J/K-atom, discrepancies remain between calculated and experimentally determined slopes for GAF. The discrepancy is greater if there is no Al–Si disorder in anorthite. High temperature thermodynamic data for almandine and grossular are needed to help resolve this problem.     

Mg-Fe partitioning between biotite and a supercritical chloride solution

An experimental study of the partitioning of Mg and Fe between synthetic biotite and an aqueous chloride solution in the supercritical region as a function of temperature, pressure and concentration of Mg and Fe is reported. In the temperature range 500°–700° C and the pressure range 25–200 MPa, the Mg-Fe distribution between biotite and the chloride solution can be described by distribution curves based on the ideal solution model within a data scattering of 8%. Mg is preferentially partitioned into biotite, and Fe prefers the solution. This tendency is enhanced with increasing temperature. The distribution constants for the Mg-Fe exchange reactions in the system K(Mg,Fe)₃AlSi₃O₁₀(OH)₂-(Mg,Fe)Cl₂-KCl-H₂O have been determined. The present data favor a model in which the activity of Fe and Mg in biotite is close to the mole fraction at temperatures above 500° C. Comparison of the Mg-Fe partitioning between biotite-chloride solution and olivine-chloride solution reveals a slight enrichment of Fe in olivine relative to biotite.