Reaction Between Ultramafic Rock and Fractionating Basaltic Magma II. Experimental Investigation of Reaction Between Olivine Tholeiite and Harzburgite at 1150-1050?C and 5 kb

We present results of experiments on mixtures of olivine tholeiiteand mantle harzburgite, at 5 kb and 1050–1150?C, underconditions of controlled hydrogen fugacity. The basalt end-memberwas Kilauea 1921 olivine tholeiite+3 wt.% H₂O, and the harzburgiteend-member was a mixture of olivine and orthopyroxene mineralseparates made from a mantle-derived lherzolite xenolith. Theexperiments on mixtures of basalt and harzburgite difl not reachequilibrium in runs ranging from 12 to 200 h duration. Relativelylarge concentration gradients persisted in both liquid and solidphases in mixed samples, whereas ‘control’ samplescontaining only basalt were reasonably homogeneous and wereprobably close to equilibrium. Compositions of solid phases produced, measured by electronmicroprobe, show a regular increase in Mg/(Mg+Fe) with increasingproportion of harzburgite at constant temperature, but olivineand clinopyroxene in mixed samples were not in Fe-Mg exchangeequilibrium. Modes measured for each sample show that the fractionof liquid relative to the amount of basalt in the sample wasconstant at constant temperature, and independent of bulk composition:reaction between 1921 basalt and harzburgite does not changethe mass of liquid in the system. Average experimental liquidcompositions for each sample were obtained by mass balance.Using Kds defined by the ‘control’ sample for eachtemperature, and mass balance constraints, phase assemblages(solid- and liquid-phase compositions and proportions) werecalculated for all mixtures. Whether samples included harzburgite or not, all average experimentalliquid compositions, and all predicted liquid compositions,for samples run at 1050?C, are high-alumina basalts by the definitionof Kuno (1960). By the criteria of Irvine & Baragar (1971),all but two average experimental liquid compositions in basalt-harzburgitemixtures, and all predicted liquid compositions in basalt-harzburgitemixtures, are calc-alkaline basalts and basaltic andesites,whereas liquids in samples containing only basalt are tholeiiticbasalts. Combined crystallization and reaction with harzburgitein the upper mantle will produce calc-alkaline derivative liquidsfrom an olivine tholeiite liquid under conditions of temperature,pressure, water and oxygen fugacity, and initial bulk compositionwhich would produce a tholeiitic liquid line of descent by crystallizationin a closed system. ^*Present address: Woods Hole Oceanographic Institution, Woods Hole, Massachusetts 02543Present address: Grant Institute of Geology, University of Edinburgh, West Mains Road, Edinburgh EH9 3JW, UK     

A Crustal Progenitor for the Intrusive Anorthosite--Charnockite Kindred of the Cupriferous Koperberg Suite, O'okiep District, Namaqualand, South Africa; New Isotope Data for the Country Rocks and the Intrusives

The Koperberg Suite comprises some 1700 small bodies of intrusiverocks largely composed of andesine anorthosite, biotite diorite,and leuconorite, norite and melanorite-hypersthenite; 30 mineshave been established in the O'okiep District in the cupriferousrocks of this anorthosite-charnockite kindred. The suite isintrusive into a sequence of granite gneiss and metavolcanicand metasedimentary rocks, and intrusive granite, that wereelevated to the granulite fades of regional metamorphism.TheSm-Nd model ages for the country rocks and the Koperberg Suiteare all 1700 Ma (T_CHUR) and 2000 Ma (T_DM) supporting a majorcrustforming event in this portion of Namaqualand at the endof Lower Proterozoic times. The granulite fades metamorphismin the O'okiep District is recorded by a Rb-Sr isochron ageof 1223 48 Ma on the Nababeep Granite Gneiss, and by (1197 15)-Ma-old inherited cores of zircons in the Koperberg Suite.The time of intrusion of the Concordia and Rietberg Granitesis believed to be reflected by their Rb-Sr whole-rock age of1105 24 Ma. The mean U-Pb age of 1029 10 Ma on individualzircon grains and zircon rims from the Koperberg Suite recordsthe time of its intrusion, and this is supported by the Sm-Ndwhole-rock age of 1022 42 Ma for the suite. Subsequent coolingand reheating events are recorded by the Ar-Ar ages of 800–850Ma for the Koperberg Suite, and of 500–550 Ma for thesuite and certain country rocks, respectively.An Nd value of-7,and its volume and composition, suggest a crustal-melt sourcefor the intrusive Concordia Granite. Moreover, the age-correctedhigh l_Sr (07061-07272) and low Nd (-9), and the high µ₂(101), that characterize the Koperberg Suite also imply a crustalsource, and a model is presented for the generation of the majorpart of the suite by partial melting of granulites of overallintermediate (diorite) composition in the lower crust. Corresponding author     

Palaeo‐climate controlled diagenesis of the Westphalian C & D fluvial sandstones in the Campine Basin (north‐east Belgium)

The Westphalian C and D fluvial sandstones in the Campine Basin (north‐east Belgium) are potential reservoirs for the sequestration of CO₂ and interesting analogues of the hydrocarbon reservoirs in the Southern North Sea. Although these sandstones were deposited in a relatively short period of time, their reservoir properties and mineralogical compositions are very different. A petrographic study complemented with stable isotope analyses, fluid inclusion microthermometry and X‐ray diffraction analyses of the clay fractions of the sandstones, which were sampled from deep boreholes (>1000 m) in the Campine Basin, revealed that these differences are related mainly to the climate at the time of deposition. The most important eogenetic processes affecting the Westphalian sandstones were the generation of a pseudomatrix by physical compaction of Al‐silicates and lithic fragments that were strongly altered by extensive meteoric leaching, kaolinitization of unstable silicates and precipitation of siderite. These processes had a detrimental influence on the reservoir properties of Westphalian C sandstones, but their impact on the Westphalian D sandstones was minimal. The difference is assumed to be related to the climate at the time of deposition, which changed from tropical humid in the Westphalian C to semi‐arid/arid during the Late Westphalian D. Both the Westphalian C and D sandstones were affected by similar mesogenetic processes. Mesogenetic quartz cementation resulted from chemical compaction and illitization of kaolinite, K‐feldspar and smectitic clays. Illitization of kaolinite was controlled by the available quantities of co‐existing kaolinite and K‐feldspar and mainly affected the Westphalian D sandstones. Illitization of K‐feldspar was controlled by the K‐feldspar content. It had a much larger impact on the reservoir properties of the Westphalian D as, in these sandstones, K‐feldspar was less affected by eogenetic alteration. The illitization of smectitic clays resulted in illite, quartz and ankerite cementation in both reservoirs. This process had a more important impact on the Westphalian C reservoir, since cementation here also resulted from smectite to illite conversion in the interbedded and underlying shales. The effect of mesogenetic alterations on the reservoir properties was much less drastic than the impact of eodiagenesis. Mesogenetic alterations do exert a significant control on the properties of the Westphalian D. The vast impact of eodiagenesis on the Westphalian C sandstones made them less susceptible to mesogenetic alteration. The effect of telogenetic processes on the porosity and permeability of the Westphalian sandstones was small and restricted to the top reservoir intervals that directly underlie the Cimmerian Unconformity. No significant telogenetic alterations related to the Variscan Unconformity were observed.