A Strontium Isotopic Investigation of the Bjerkreim--Sokndal Layered Instrusion, Southwest Norway

The 230 km² Proterozoic Bjerkreim—Sokndal layered instrusionhas a monzonoritic bulk composition and comprises a 6 km thick,broadly leuconoritic Layered Series (LS) overlain by unlayeredmangerite and quartz mangerite. In the Bjerkreim lobe the LScomprises six megacyclic units (MCU 0, IA, IB, II, 11 and IV)in a syncline. This lobe is surrounded by migmatitic gneisses;the roof to the instrusion is missing. The mg-number opx, An% and whole-rock initial ⁸⁷Sr/⁸⁶Sr isotope ratios (Sr₀) displaybroadly parallel trends through MCUs II and III, and into MCUIV, with decreasing mg-number (75–58) and An % (50–40)accompanying increasing Sr₀ (0.7050–0.7085). This correlationbreaks down in the upper part of MCU IV and mangerite; the quartzmangerite has Sr₀ values of 0.7085. Abrupt reversals occur acrossthe MCU boundaries. The LS crystallized on the floor of a periodically replenishedmagma chamber that was continually assimilating country rockgneisses. Strong compositional zoning of the magma developedas a result of repeated replenishments with relatively dense,primitive ferrobasaltic magma (Sr₀ = 0.7049) along the floorand the development of extensive buoyant roof melts. Assimilationtook place on a massive scale (up to 50%) in the upper partsof the chamber. KEY WORDS: assimilation; fractional crystallization; hybrid magma; layered intrusion; Sr-isolopes ^*Corresponding author.     

Temperate shelf carbonate sediments in the Cenozoic of New Zealand

Shelf limestones are widely distributed in New Zealand Cenozoic sequences and are especially well developed in the Oligocene. Detailed field and laboratory work on several Oligocene occurrences, and reconnaissance field-work at most other sections have elucidated the major characteristics of the environment, texture, composition and diagenesis of these sediments. Several generalizations emerge which contrast with the commonly accepted characteristics of shallow marine carbonate sedimentation established from studies of tropical and subtropical deposits. The limestones are either calcarenites or, less commonly, calcilutites and, in general, these two lithologies are mutually exclusive, both in time and space. The allochems and interparticle carbonate mud (where developed) in calcarenitic limestones consist almost exclusively of fragmented skeletal material derived primarily from bryozoan, echinodermal, benthic foraminiferal, barnacle, brachiopod, bivalve and coralline red algal tests. The calcilutitic limestones consist mainly of whole and disintegrated tests of pelagic foraminifers and coccolithophorids. Non-skeletal carbonate components such as ooids, pellets and aggregates are conspicuously absent from both lithologies. Reefal structures are also absent or rare and are mainly oyster reefs. The limestones commonly contain a significant content of terrigenous material and/or glauconite and at the stratigraphic level the limestones are intimately associated with terrigenous formations. The distribution of the carbonate sediments has been governed mainly by rate of supply of river-derived terrigenous material, by subsequent dispersal patterns of this material over the shelf, and by current sorting. As a consequence of selective grain transport, bedding in the limestones is often defined by the cyclic alternation on a wide range of scales of carbonate units that are relatively enriched and relatively impoverished in terrigenous material. The primary (carbonate) mineralogy of the carbonate sediments was completely dominated by magnesium calcite and/or calcite with only small amounts of aragonite and no dolomite or associated evaporite minerals. The metastable magnesium calcite and aragonite grains were probably altered on, or close below, the shallow sea-floor. Among other factors, transformation was encouraged by the absorption of magnesium in pore waters by montmorillonitic clays and by the complete oxidation of all organic matter in the bottom sediments. Magnesium calcite grains were stabilized by texturally non-destructive incongruent dissolution, but aragonite was often dissolved without trace from the sediment, especially in grainstones. Thus submarine diagenesis has been characterized by selective dissolution phenomena. Cementation by granular and syntaxial rim orthosparite of calcite and/or ferroan calcite composition occurred mainly during shallow subsurface burial and was associated with the intergranular solution of calcitic skeletal fragments, especially at those levels in the sediment relatively enriched in terrigenous material. This lithification process has worked to accentuate and modify original litho-logic differences and sedimentary structures in the primary sediments and has produced a kind of rhythmic vertical alternation of less well cemented, microstylolitized, impure limestone beds (‘cement-donor’ beds) and well cemented, more open textured, purer limestone beds (‘cement-receptor’ beds). The New Zealand limestones formed between latitudes 60° S and 35° S under generally cool temperate to warm temperate climate conditions. Oxygen isotopes suggest that surface waters were mainly significantly cooler than 20°C, so that shelf waters may have experienced extended periods of undersaturation with respect to calcium carbonate. Generally open circulation patterns maintained near normal salinity values over the entire shelf platform. Calculated sedimentation rates for the New Zealand carbonate sediments are generally very low (< 5 cm/1000 years). Periods of more active deposition commonly alternated with longer periods of non-deposition and by-passing or erosion. It is concluded that many characteristics of the New Zealand shelf limestone occurrences are explained best by a temperate latitude model of shallow marine carbonate sedimentation.     

A Study of Macro-Rhythmic Layering and Cumulate Processes in the Jimberlana Intrusion, Western Australia. Part I: The Upper Layered Series

The upper layered series of the Jimberlana Intrusion rests unconformablyon the lower layered series and has resulted from a major newpulse of magma which entered the magma chamber during the finalstages of crystallization of the lower series. All parameterswhich vary systematically with fractionation are sharply reversedat the contact between the two layered series. The lower portion of the ultramafic zone of the upper layeredseries is composed of a repeated macro-rhythmic succession ofolivine cumulates, bronzite-olivine cumulates, and bronzitecumulates. A detailed investigation was made of this sequenceso that the contacts between the units could be compared withthe contact between the upper and lower layered series. Cu,Ni, Cr, P, and U were measured on a whole rock basis; the Mg/Mg?Feratios of the pyroxenes and olivines, the Cr content of pyroxenesand the Ni content of olivines were determined by the electronmicroprobe. Each of the macro-rhythmic units is associated witha reversal in mineral variation and in the Ni-Cr trends andhas a zone of high sulphide values at its base. These featuresare also found at the contact between the upper and lower layeredseries and, if the upper series is due to a new influx of magma,it follows that the macro-units are also due to multiple injection.This conclusion is strongly supported by the size of the reversalswhich are too large to be explained by the alternative hypothesesto multiple injection suggested by Jackson (1961) and Wager(1959). The anomalous sulphide-rich zones at the contacts between theupper and lower layered series and between the macro-rhythmicunits are thought to have formed from a narrow supercooled zonewhich developed for a brief period at the bottom of the magmachamber following each new magma pulse. The olivines from thesesulphide-rich zones are depleted in Ni, suggesting that Ni hasbeen scavenged by the sulphides. This is only possible if theolivine grains crystallized with the sulphides in the restrictedsupercooled zone at the bottom of the magma chamber.     

Palaeo-ice streams and the subglacial landscape mosaic of the North American mid-continental prairies

The analysis of the glacial landscape of southern Saskatchewan (Canada) through multiple data sets (e.g. digital elevation model, till compositional data) has revealed previously unrecognized subglacial sediment–landform assemblages. A southwest-trending corridor of mega-scale till lineations (Maskwa corridor) bounded on each side by hummocky terrain extends from the Canadian Shield to southwestern Saskatchewan. This landform assemblage is clearly cross-cut by a broad south to southeast trending corridor (Buffalo corridor) consisting of subparallel curvilinear till ridges. The carbonate content of the surface till is spatially consistent within these assemblages, suggesting a strong sediment–landform relationship. The two corridors are interpreted as the product of palaeo-ice streams. The Maskwa palaeo-ice stream flowed up the regional slope and across preglacial valleys, indicating it was thick and stable. Narrow dispersal trains extending across as well as down-glacier from the Athabasca Basin suggest that the Maskwa palaeo-ice stream extended far into the ice sheet across contrasting shield and platform terrains. In comparison, the Buffalo palaeo-ice stream was thinner and largely controlled by subglacial geology and topography. Its catchments were located at the Canadian Shield boundary and the system was oriented along-slope. It experienced lateral shifts and it was fed by a network of tributaries. The glacial dynamics shift from the Maskwa to the Buffalo system occurred at about 13.5 ¹⁴C kyr BP. The Buffalo system later evolved into thin outlet lobes until final deglaciation of the area. The proposed model has implications for ice-sheet reconstruction and the assessment of till properties in the prairies and in similar terrains.     

Spatial and Temporal Validation of In-Situ and Satellite Weather Data for the South West Agricultural Region of Australia

Seasonal variations in weather have significant impacts on crop yields. The accuracy of weather data is an import-ant consideration for crop yield models. This ...     

Pluriactivity in (and beyond?) a Regulationist Crisis

The study of rural pluriactivity in New Zealand has been based on the assumption that it is a temporary phenomenon: a survival strategy in times of crisis. This paper seeks to position both pluriactivity and ‘rural crisis’ in a more sound theoretical framework by referring to recent work in regulation theory. Case studies from the Mid-Canterbury and Catlins areas are used to suggest the role that pluriactivity may fulfil in any future mode of growth in rural New Zealand. In doing so, questions are raised regarding rural ideology and agency in the process of economic change.     

Petrology of the G and H Chromitite Zones in the Mountain View Area of the Stillwater Complex, Montana

The Ultramafic Series of the Stillwater Complex in the MountainView area of the intrusion consists of 17 cyclic units thathave been numbered stratigraphically. A typical unit has olivinecumulates at the base, olivine–bronzite cumulates at intermediatelevels, and bronzite cumulates at the top. Most cyclic unitsalso have chromite-rich layers near their base, the thickestbeing the G and H chromitite zones in units 10 and 11. The Gand H zones are each separated from the top of the underlyingcyclic unit by 1–3 m of coarse-grained olivine cumulateand pegmatite; and they are both succeeded by thinner chromititezones, respectively called the hanging wall G (HWG) and thehanging wall H (HWH) zones, situated {small tilde}20 m and 5m above them. The G and H chromitite zones feature rhythmicsequences of thin layers that tend to progress upward from massivechromitite through chromite–olivine cumulate to olivine–chromitecumulate (the last with the minerals in approximately cotecticproportions of about 98:2). In cyclic units 10 and 11, variationsof Mg/Fe in the olivine and bronzite, and of Ni in the olivine,are small and show no clear stratigraphic fractionation trends.The abundance of Cr in the chromite in unit 10 does have a fractionationtrend, however, being generally highest at the bottom of theunit and lowest at the top, with a regression at the HWG zone.In general, Cr in chromite is highest at the base of a rhythmicunit and decreases upward, but it shows no overall decline throughsuccessive rhythmic units; Fe³ exhibits opposite variation,being lowest in the massive chromite, and highest in the disseminatedgrains. The G and H chromitite zones, in the Mountain View area, eachcontain enough chromite to form a single layer of massive chromitite{small tilde} 1 m thick. If their formation involved removalof only 30% of the Cr in the parental magmatic liquid (estimatedconcentration, 600 ppm), then this liquid could have amountedvolumetrically to an areally equivalent layer at least 2000m thick. Model calculations demonstrate that such a large volumeof liquid is consistent with the small variations of Mg/Fe inthe pyroxenes and olivines in the Stillwater cyclic units. We postulate that the G and H chromitite zones and cyclic unitsthat host them formed in response to the entry of new pulsesof primitive magmatic liquid into the Stillwater chamber. Fromexperimental observations, we infer that these pulses producedfountains in which the primitive liquid mixed with residualfractionated liquids, yielding hybrids that were compositionallywithin the chromite liquidus field (or volume) and that weresupercooled (supersaturated ) with respect to the oxide mineral.These effects may have been enhanced by low fO₂ (oxygen fugacity)in the primitive liquid and(or) by high fO₂ of the fractionatedliquid. The hybrid liquids probably collected at the bottomof the chamber in a zoned layer that then divided into double-diffusiveconvecting layers. In these circumstances, the lowest chromite-richlayer in a rhythmic sequence could have formed from the lowestdouble-diffusive liquid layer, and the next could then haveformed when this liquid mixed with the liquid layer above it—andso on up the sequence. We argue that the thick G and H chromititezones are situated toward the top of the Ultramafic Series becausethat level marks when the compositional contrasts between theinjected primitive liquid and the residual fractionated liquidsin the chamber were greatest.