P–T–fluid evolution in the Mahalapye Complex, Limpopo high-grade terrane, eastern Botswana

Metapelites, migmatites and granites from the c. 2 Ga Mahalapye Complex have been studied for determining the P–T–fluid influence on mineral assemblages and local equilibrium compositions in the rocks from the extreme southwestern part of the Central Zone of the Limpopo high‐grade terrane in Botswana. It was found that fluid infiltration played a leading role in the formation of the rocks. This conclusion is based on both well‐developed textures inferred to record metasomatic reactions, such as Bt ? And + Qtz + (K₂O) and Bt ± Qtz ? Sil + Kfs + Ms ± Pl, and zonation of Ms | Bt + Qtz | And + Qtz and Grt | Crd | Pl | Kfs + Qtz reflecting a perfect mobility (Korzhinskii terminology) of some chemical components. The conclusion is also supported by the results of a fluid inclusion study. CO₂ and H₂O ( = 0.6) are the major components of the fluid. The fluid has been trapped synchronously along the retrograde P–T path. The P–T path was derived using mineral thermobarometry and a combination of mineral thermometry and fluid inclusion density data. The Mahalapye Complex experienced low‐pressure granulite facies metamorphism with a retrograde evolution from 770 °C and 5.5 kbar to 560 °C and 2 kbar, presumably at c. 2 Ga.     

Neotectonics, sea-level changes and biological evolution in the Fennoscandian Border Zone of the southern Kattegat Sea

Shallow seismic data and vibrocore information, sequence stratigraphic and faunal evidence have been used for documentation of Late Weichselian reactivation of faulting in the south central Kattegat, southern Scandinavia. The study area is situated on the Fennoscandian Border Zone, where tectonic activity has been recurrent since Early Palaeozoic time and still occurs, as shown by present earthquake activity. New data from the area south of the island of Anholt show that after deglaciation fast isostatic rebound resulted in reactivation of a NW-SE striking normal fault system. This tectonic episode is dated to a period starting shortly before 15.0 cal. ka BP and ending around 13.5 cal. ka BP, after regression had already reached a level of about 30 m b.s.l. The vertical displacement associated with the faulting was in the order of 20 m. More generally, the results support the previously reported late Weichselian sea-level highstand, which was followed by forced regression until the eustatic sea-level rise surpassed the rate of glacio-isostatic rebound in early Preboreal. Our findings further imply that drainage of the Baltic Ice Lake through the Øresund at c. 15 cal. ka BP (Bergsten & Nordberg 1992) may have been triggered by tectonic activity in this region.     

Playa‐lake sedimentation and organic matter accumulation in an Andean piggyback basin: the recent record from the Cuenca de Pozuelos,North‐west Argentina

Expansive playa‐lake systems situated in high‐altitude piggyback basins are important and conspicuous components of both modern and ancient cordilleran orogenic systems. Extant playa lakes provide vital habitat for numerous endemic species, whereas sediments from these deposystems may record signals of climate change or develop natural resources over geological time. Laguna de los Pozuelos (North‐west Argentina) provides the opportunity for an actualistic sedimentological and geochemical assessment of a piggyback basin playa lake in an area of critical interest for understanding Quaternary palaeoclimate dynamics. Silty clays and diatom ooze are the dominant playa‐lake centre microfacies, with concentrations of total organic carbon and biogenic silica commonly exceeding 1·5 wt% in this sub‐environment. Elemental and stable isotopic analyses point to a mixed organic matter composition in the playa‐lake centre, with substantial contributions from algae and transported aquatic macrophytes. Bulk sediment and organic mass accumulation rates in the southern playa‐lake centre approach 0·22 g cm^?2 year^?1 and 2·89 mg cm^?2 year^?1, respectively, indicating moderately rapid deposition with negligible deflation over historic time. Playa margin facies contain higher percentages of fragmented biogenic carbonate (ostracods and charophytes) and inorganically precipitated aragonite crusts due to seasonal pumping and evaporation of ground water. Organic matter accumulation is limited along these heavily bioturbated wet and dry mud flats. Fluvial–lacustrine transitional environments, which are key waterbird habitats, are either silty terminal splay (northern axis) or sandy deltas (southern axis) containing highly oxidized and partially allochthonous organic matter. Modern analogue data from Laguna de los Pozuelos provide key insights for: (i) environmental reconstructions of ancient lake sequences; and (ii) improving facies models for piggyback basins.     

Petrology and Geochemistry of the Rhobell Volcanic Complex: Amphibole-Dominated Fractionation at an Early Ordovician Arc Volcano in North Wales

The Rhobell Volcanic Complex is a remnant of a late Tremadoc,dominantly calc-alkaline, arc volcano. It is the only substantiallypreserved representative in the southern British Caledonidesof an early phase of Ordovician ensialic arc volcanism whichfollowed the onset of southeasterly subduction of Iapetus oceaniclithosphere beneath the northern margin of Gondwanaland. Thecomplex includes extrusive basalts and associated breccias,known as the Rhobell Volcanic Group, which rest unconformablyon folded, uplifted and eroded rift-basin sediments of the earlierpassive margin of the Iapetus Ocean. Amongst the basalts arerelatively primitive pargasite-bearing varieties which containcognate cumulate blocks, dominantly of pargasite but also withcalcic clinopyroxene, Ti-magnetite, and (rarely) plagioclase.Basaltic rocks also occur in an associated feeder-sheet intrusioncomplex, and as numerous minor sills and dykes. In the intrusioncomplex, basaltic sheets are cut by microdiorites and scarcemicrotonalites. The compositional range in the volcanic complex,from low-SiO₂ basalts to microtonalites (SiO₂ 45–66 wt.per cent), is attributable to fractional crystallization, earlystages of which were dominated by removal of pargasite at (water-undersaturated)pressures close to 10 kb, within the mantle. The parental magmawas derived by hydrous partial melting of a supra-subductionzone mantle wedge. Trace-element patterns indicate that themantle was slightly depleted relative to the putative primordialcomposition (Ta/Yb = 0?1), prior to metasomatism by componentsfrom the subduction zone. Textural variations in cumulate blocks,and various phenocryst forms in basalts, are interpreted asindicating that the erupted magmas came from a thermally andcompositionally stratified magma chamber with associated layeredcrystal accumulations, and that materials from initially separatelayers were mixed prior to eruption.     

Controlling factors of volumetrically important marine carbonate cementation in deep slope settings

The controlling parameters of early marine carbonate cementation in shoal water and hemipelagic to pelagic domains are well‐studied. In contrast, the mechanisms driving the precipitation of early marine carbonate cements at deeper slope settings have received less attention, despite the fact that considerable volumes of early marine cement are present at recent and fossil carbonate slopes in water depths of several hundreds of metres. In order to better understand the controlling factors of pervasive early marine cementation at greater water depths, marine carbonate cements observed along time‐parallel platform to basin transects of two intact Pennsylvanian carbonate slopes are compared with those present in the slope deposits of the Permian Capitan Reef and Neogene Mururoa Atoll. In all four settings, significant amounts of marine cements occlude primary pore spaces downslope into thermoclinal water depths, i.e. in a bathymetric range between some tens and several hundreds of metres. Radial, radiaxial and fascicular optic fibrous calcites, and radiaxial prismatic calcites are associated with re‐deposited facies, boundstones and rudstones. Botryoidal (formerly) aragonitic precipitates are common in microbially induced limestones. From these case studies, it is tentatively concluded that sea water circulation in an extensive, near‐sea floor pore system is a first‐order control on carbonate ion supply and marine cementation. Coastal upwelling and internal or tidal currents are the most probable mechanisms driving pore water circulation at these depths. Carbonate cements precipitated under conditions of normal to elevated alkalinity, locally elevated nutrient levels and variable sea water temperatures. The implications of these findings and suggestions for future work are discussed.     

Identifying Accessory Mineral Saturation during Differentiation in Granitoid Magmas: an Integrated Approach

Numerical reconstructions of processes that may have operatedduring igneous petrogenesis often model the behaviour of importanttrace elements. The geochemistry of these trace elements maybe controlled by accessory mineral saturation and fractionation.Determination of the saturation point of accessory mineralsin granitoid rocks is ambiguous because assumptions about crystalmorphology and melt compositions do not always hold. An integratedapproach to identifying accessory mineral saturation involvingpetrography, whole-rock geochemical trends, saturation calculationsand mineral chemistry changes is demonstrated here for a compositionallyzoned pluton. Within and between whole-rock samples of the BoggyPlain zoned pluton, eastern Australia, the rare earth element(REE)-enriched accessory minerals zircon, apatite and titaniteexhibit compositional variations that are related to saturationin the bulk magma, localized saturation in intercumulus meltpools and fractionation of other mineral phases. Apatite isidentified as having been an early crystallizing phase overnearly the whole duration of magma cooling, with zircon (andallanite) only saturating in more felsic zones. Titanite andmonazite did not saturate in the bulk magma at any stage ofdifferentiation. Although some trace elements (P, Ca, Sc, Nb,Hf, Ta) in zircon exhibit compositional variation progressingfrom mafic to more felsic whole-rock samples, normalized REEpatterns and abundances (except Ce) do not vary with progressivedifferentiation. This is interpreted to be a result of limitationsto both simple ‘xenotime’ and complex xenotime-typecoupled substitutions. Our data indicate that zircon REE characteristicsare not as useful as those of other REE-rich accessory mineralsas a petrogenetic indicator. KEY WORDS: saturation; zircon; apatite; titanite; magma differentiation; trace elements; REE patterns     

Diagenetic processes in Holocene carbonate sediments: Florida Bay mudbanks and islands

The sedimentology, mineralogy and pore fluid chemistry of seven cores from the Holocene sediments of Florida Bay were studied to determine the physical processes and diagenetic reactions affecting the sediments. The cores were taken in a transect from a shallow mudbank onto a small adjacent island, Jimmy Key. Steady state models of pore fluid chemistry are used to estimate the rates of various reactions. In the mudbank sediments, little carbonate mineral diagenesis is taking place. No change in sediment mineralogy is detectable and pore water profiles of Ca²⁺, Mg²⁺ and Sr²⁺ show only minor variation. Chloride concentrations indicate substantial biological mixing of seawater from the bay into the sediments in one of the cores. Pore water analyses of sulphate and alkalinity show only a low degree of sulphate depletion and a decreasing extent of sulphate reduction downcore. Models of sulphate reduction in the mudbank show that there is substantial chemical exchange between the sediment pore fluids and water from the bay probably as a result of bio-irrigation. The sulphate and alkalinity data also suggest that the underlying Pleistocene rocks contain water of near normal seawater composition. Stratigraphic analysis and δ¹³C analyses of the organic carbon in the sediments of the island cores show that the sediments were primarily deposited in a subtidal mudbank setting; only the upper 20–30 cm is supratidal in origin. Nevertheless, island formation had a significant effect on pore fluid chemistry and the types of diagenetic reactions throughout the sediment column. Chloride in the sediment pore fluids is more than twice the normal seawater concentrations over most of the depth of the cores. The constant, elevated chloride concentrations indicate that hypersaline fluids which formed in ponds on the island are advected downward through the sediments. Models of the chloride profiles yield an estimate of 2·5 cm yr^?1 as a minimum advective velocity. Changes in pore water chemistry with depth are interpreted as indicating the following sequence of reactions: (1) minor high-Mg calcite dissolution and low-Mg calcite precipitation, from 0 to 35 cm; (2) Ca- or Mg-sulphate dissolution and low-Mg calcite precipitation, from 5 to 35 cm; (3) dolomite or magnesite precipitation together with sulphate reduction, from 35 to 55 cm; and (4) little reaction below 55 cm. In addition, one or more as yet unidentified reactions must be taking place from 5 to 55 cm depth as an imbalance in possible sources and sinks of alkalinity is observed. The imbalance could be explained if chloride is not completely conservative. Despite the pore fluid chemical evidence for diagenetic reactions involving carbonate minerals, no changes in sediment mineralogy were detected in X-ray diffraction analyses, probably because of the comparatively young age of the island.     

Melting Relationships in the System CaO-MgO-CO2-H2O, with Petrological Applications

Phase relationships on the vapor-saturated liquidus surfacein the system CaO-MgO-CO₂-H₂O have been deduced from data inthe systems CaO CO₂-H₂O, CaO-MgO-CO₂, and MgO-CO₂-H₂O, and frompreliminary experiments in the quaternary system. These areillustrated in composition tetrahedra, and in isobaric sectionsthrough the petrogenetic model. The univariant PT curve forthe beginning of melting lies between 625? C and 600? C in thepressure range 10 bars to 4 kilobars, in the presence of a vaporphase rich in H₂O. The curve is divided into three sectionsby two invariant points, each section having a different primarymagnesian phase involved in the melting reaction. Periclaseoccurs on the low-pressure section (less than about 1 kilobar),and with increasing pressure first brucite and then dolomitebecome stable on the liquidus. The pressure of the second invariantpoint, above which dolomite is stable on the liquidus, is notknown. The effect of FeO as an additional component is considered.Processes of crystallization resulting from changes in temperature,in pressure, and in the composition of the vapor phase are discussed.These processes are applied to the crystallization and differentiationof carbonatite magmas, and the reverse processes involving fusionare applied to the metamorphism of dolomites. Crystallizationdifferentiation of a carbonatite magma could produce the sequenceof intrusion observed at some carbonatite complexes: calcitics?vite, followed by ankeritic s?vite, and finally sideriticcarbonatite. Partial melting may occur during the thermal metamorphismof dolomites, but melting is unlikely during regional metamorphism.