Alkaline lamprophyre and related dyke rocks in NE Transdanubia,Hungary: The Alcsutdoboz-2 (AD-2) borehole

Summary The Alcsutdoboz-2 (AD-2) core contains 12 magmatic dykes which belong to the Late Cretaceous lamprophyric-carbonatitic association of NE Transdanubia, Hungary. Petrographically, 11 dykes can be considered alkaline lamprophyre (mainly monchiquite), and the remainder might be called carbonatite. The lamprophyre dykes are similar to both alkaline lamprophyres and ultramafic lamprophyres in major element composition, whereas the carbonatite dyke has some features that are similar to carbonatites but others that are dissimilar. Nevertheless, both of the two types of AD-2 dykes possess higher LILE content than the ultramafc lamprophyres and kimberlites, but strongly differ from average carbonatite. Based on the REE pattern, crystal fractionation (mainly of olivine) and separation of a carbonate phase from the parental lamprophyric magma are proposed for genesis of the carbonatite dyke. These characteristics and the compositional zoning of clinopyroxene and mica suggest a complex crystallization history for these dykes. The likeliest origin for the parental lamprophyric melt is through a very small degree of partial melting of metasomatized mantle.

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Alkalische Lamprophyre und assoziierte Ganggesteine in Nordost-Transdanubien, Ungarn: die Bohrung Alcsutdoboz-2 (AD-2)

Zusammenfassung Der Kern der Bohrung Alcsutdoboz-2 (AD-2) enthält zwölf magmatische Gänge, die zu der jung-kretazischen Lamprophyr-Karbonatit-Assoziation des nordöstlichen Transdanubiens in Ungarn gehören. Petrographisch gesehen gehören elf Gänge zu den alkalischen Lamprophyren (hauptsächlich Monchiquit), und der Rest kann als Karbonatit bezeichnet werden. Die Lamprophyrgänge sind in ihrer Hauptelementzusammensetzung sowohl alkalischen Lamprophyren wie ultramafschen Lamprophyren ähnlich. Der Karbonatitgang hingegen zeigt Parameter, die denen von Karbonatiten teilweise, aber nicht durchwegs, ähnlich sind. Beide Typen der AD-2-Gänge zeigen höhere LILE-Gehalte als ultramafische Lamprophre und Kimberlite, unterscheiden sich aber deutlich vom durchschnittlichen Karbonatit. Auf der Basis der Seltenen ErdVerteilung, werden Kristallfraktionierung (hauptsächlich von Olivin) und Abtrennung einer Karbonatphase von lamprophyrischen Magma als Vorgänge gesehen, die für die Entstehung der Karbonatit-Gänge relevant sind. Diese Aspekte und die Zonierung der Zusammensetzungen von Klinopyroxen und Glimmer weisen auf eine komplexe Kristallisationsgeschichte dieser Gänge hin. Sehr wahrscheinlich ist die lamprophyrische Ausgangsschmelze durch eine geringfügige teilweise Aufschmelzung von metasomatisiertem Mantel entstanden.

     

Anisotropy of magnetic susceptibility parameters: Guidelines for their rational selection

Twenty-eight parameters used to characterize measurements of the anisotropy of magnetic susceptibility are compared theoretically in this work by introducing the concept of the field of susceptibility tensors, which allows the representation of parameters as families of lines in a plane. It is demonstrated that the foliation and lineation parameters are but a special case of the shape parameters, implying that the resolution of these two rock fabric elements using AMS measurements alone is more an artifact of the numerical range of definition of some parameters than a quantification of two physically independent features. Also, it is shown that parameters presumably of the same type do not necessarily yield equivalent interpretation of results in a qualitative sense, and therefore, caution should be strongly exercised when parameters are to be selected. Paramters quantifying the degree of anisotropy are, in general, equivalent to each other because of the very small departure observed in natural rocks from the isotropic case. However, a final consideration of the possible ability to differentiate rock types and a convenient range of values allowing expression of the degree of anisotropy in a well-defined percentage are pointed out as the main factors to be considered before selecting one parameter within this class.     

Seismic activity related to the 1991 eruption of Colima Volcano,Mexico

Ten years after the last effusive eruption and at least 15 years of seismic quiescence, volcanic seismic activity started at Colima volcano on 14 February 1991, with a seismic crisis which reached counts of more than 100 per day and showed a diversity of earthquake types. Four other distinct seismic crises followed, before a mild effusive eruption in April 1991. The second crisis preceded the extrusion of an andesitic scoriaceous lava lobe, first reported on 1 March; during this crisis an interesting temporary concentration of seismic foci below the crater was observed shortly before the extrusion was detected. The third crisis was constituted by shallow seismicity, featuring possible mild degassing explosion-induced activity in the form of hiccups (episodes of simple wavelets that repeat with diminishing amplitude), and accompanied by increased fumarolic activity. The growth of the new lava dome was accompanied by changing seismicity. On 16 April during the fifth crisis which consisted of some relatively large, shallow, volcanic earthquakes and numerous avalanches of older dome material, part of the newly extruded dome, which had grown towards the edge of the old dome, collapsed, producing the largest avalanches and ash flows. Afterwards, block lava began to flow slowly along the SW flank of the volcano, generating frequent small incandescent avalanches. The seismicity associated with the stages of this eruptive activity shows some interesting features: most earthquake foci were located north of the summit, some of them relatively deep (7–11 km below the summit level), underneath the saddle between the Colima and the older Nevado volcanoes. An apparently seismic quiet region appears between 4 and 7 km below the summit level. In June, harmonic tremors were detected for the first time, but no changes in the eruptive activity could be correlated with them. After June, the seismicity decreasing trend was established, and the effusive activity stopped on September 1991.     

Emission of nitric oxide from soils and termite nests in a Trachypogon savanna of the Orinoco basin

Nitric oxide fluxes from soils in the Trachypogon savanna of the Orinoco basin were determined during the dry season using the static chamber method. The emission from dry soils fluctuated from 0.4 to 3 ng N m^–2 s^–1 and increased up to 25 ng N m^–2 s^–1 after moderate watering or light rain-falls (1 to 5 mm). The mean emission values are up to 6 times lower than one observed earlier at the Chaguaramas site, but up to 10 times higher than one recorded at the Guri site, indicating an important spatial variability in NO fluxes of the Venezuelan savanna region. The changes observed after the addition of nitrogen to the soil, in the form of ammonium and/or nitrate, indicate a high denitrification potential in this acidic soil. Burning of the surface vegetation produced an increase by a factor of 10 in the emission rate of NO, but the effect was relatively short in time, about 5 days. It was estimated for the savanna region that burning increases the total NO soil emission during the dry season by 15% compared to the unburnt case. Soils with termite nests emit 10 times more NO than soil without nests, but the contribution from this source is less than 2% of the total savanna soil flux.     

Probabilistic compressive strength of sound dry granite

Summary The different functions of cumulative probability of fracture that can be used in the Probabilistic Strength of Materials in the case of constant uniaxial compression are described. Sound fine-grained granite was used to study volume influence by fracturing rectangular prisms, and then no noticeable influence was observed. Since this is showing that all the fracture stresses are belonging to a single set they were included in a single group that exhibited two functions of specific risk of fracture. The population with the lesser fracture stress has no critical zone while the other population does have it and a critical zone in the order of 10^–6 m³ is the minimum size exhibiting a complete fracture of the specimen when the same collapses. All the statistical functions were found to be acceptable according to theX ² criterion.     

Petroleum isoprenoid hydrocarbons derived from catagenetic degradation of archaebacterial lipids

The three GC coeluting C₄₀ bis-phytanes with head-to-tail, tail-to-tail and head-to-head linkages considered to be archaebacterial markers, have been recognized in petroleum by enhanced mass-fragmentography. Supporting evidence has been obtained by the simultaneous occurrence of two C₂₁–C₂₄ series of isoprenoid and quasi-isoprenoid hydrocarbons that are supposedly formed during the catagenetic degradation of the isomeric C₄₀ isoprenoids. The C₂₁–C₂₄ quasi-isoprenoid hydrocarbons have been identified conclusively for the first time by comparison with authentic standards.     

Molybdenum in icelandic geothermal waters

Molybdenum concentrations in Icelandic geothermal waters lie in the range 1–70 ppb. Warm waters and dilute high-temperature waters which contain high concentrations of sulphide are lowest in molybdenum. No correlation is otherwise observed between molybdenum concentrations and temperature. Surface waters and cold ground waters do not contain detectable molybdenum (<1 ppb). It seems likely that leaching rate is the prime factor in limiting molybdenum levels in these waters. Within individual geothermal fields molybdenum concentrations are either approximately constant or they vary regularly across the field. This regular variation may often be correlated with variations in other solute concentrations and subsurface temperatures and is taken to indicate a control of molybdenum mobility by a temperature dependent equilibrium. The evidence suggests that the solubility of molybdenite is responsible. Molybdenite has not been found in active geothermal systems in Iceland but is known to occur in some New Zealand geothermal systems and it has been identified in hydrothermally altered Tertiary basalt formations at Reydarártindur in southeast Iceland. Boiling and mixing with cold water leads to molybdenite undersaturation and thus these processes favour leaching of molybdenum from the rock. On the other hand, conductive cooling leads to supersaturation which favours removal of molybdenum from solution.     

Germanium in Icelandic geothermal systems

Germanium concentrations in geothermal waters in Iceland lie mostly in the range 2–30 ppb. There is an overall positive relation between the germanium content of the water and its temperature. Most of the germanium occurs as Ge(OH)^?₅in solution but Ge(OH)₄ may also be present in significant amounts in saline waters when above 200°C. Evidence indicates that aqueous germanium concentrations are controlled by exchange reactions where it substitutes for silica in silicates and iron in sulphides. It is the rate of dissolution and the relative abundance of the alteration minerals which take up germanium to a variable extent that ultimately fix Ge(OH)₄ concentrations in the water. This, together with water pH, fixes total dissolved germanium. It is mostly the primary rock composition that dictates the relative abundance of the alteration minerals. Conductive cooling in upflow zones favours removal of germanium from solution. During the initial stages of boiling of rising hot water dissolution is enhanced but precipitation at later stages.Thermodynamic data of various aqueous germanium species and several minerals are summarized and dissociation constants and solubilities estimated at elevated temperatures using available predictive methods.     

Description and interpretation of the composition of fluid and alteration mineralogy in the geothermal system,at Svartsengi,Iceland

The bulk composition and mineralogy of hydrothermally altered tholeiite, along with the composition and speciation of fluid, have been determined for a well-defined alteration zone at 240°C and 110 bars at Svartsengi, Iceland. Mass balances between the geothermal fluid and altered tholeiite, relative to a seawater/fresh water mixture and unaltered tholeiite, indicate the overall reaction per 1000 cm³ is: 1325 gm plagioclase + 1228 gm pyroxene + 215 gm oxide-minerals break down to form 685 gm chlorite + 636 gm albite + 441 gm quartz + 249 gm epidote + 266 gm calcite + 201 gm oxide-minerals + 15 gm pyrite, requiring an influx of 123 gm CO₂, 10 gm H₂S and 4 gm Na₂O and a release of 57 gm SiO₂, 35 gm FeO, 21 gm CaO, 8 gm MgO and 4 gm K₂O.Principal reactions, deduced from textural evidence, include Na-Ca exchange in plagioclase, precipitation of quartz, calcite and anhydrite, and formation of chlorite and epidote by reactions between groundmass minerals and fluid.Thermodynamic analyses of authigenic minerals and downhole fluid indicate that the fluid maintains a state close to equilibrium with the secondary mineral phases chlorite, epidote, albite, quartz, calcite, prehnite, anhydrite, pyrite and magnetite, whereas remnant primary labradorite and augite are out of equilibrium with the fluid.Water/rock ratios for the system are determined under a variety of assumptions. However, the open nature of the system makes comparisons with experimental and theoretical closed system studies ambiguous.