Lead isotopic disequilibrium between sulfide and plagioclase in the bushveld complex and the chemical evolution of large layered intrusions

The Pb isotopic compositions of coexisting plagioclase and sulfide from the Bushveld Complex were determined by laser ablation multi-collector ICPMS (LA MC-ICPMS). The samples are of the upper Critical Zone in the northeast corner of the Complex and were collected from drill core and underground mine exposures. All the rocks are fresh and exhibit no evidence for alteration, weathering, or disruption of the Pb isotope systematics subsequent to the initial cooling of the intrusion. Furthermore, individual plagioclase and sulfide crystals do not contain enough U to warrant correction for radiogenic in-growth. For these reasons, the measured Pb isotope ratios approximate the initial ones. For plagioclase, ²⁰⁷Pb/²⁰⁶Pb ranges from 0.98 to 1.02 and ²⁰⁸Pb/²⁰⁶Pb from 2.26 to 2.35. Low ²⁰⁷Pb/²⁰⁶Pb and ²⁰⁸Pb/²⁰⁶Pb ratios characterize grain boundaries and partially annealed microcracks, some of which contain minute fragments of sulfide and other phases, and this accounts for most, if not all, the heterogeneity exhibited by individual samples. Real compositional differences exist, however, in plagioclase from different lithologic layers. For example, plagioclase ²⁰⁷Pb/²⁰⁶Pb values vary from 1.004 in norite beneath the Merensky pyroxenite to 1.009 in the mineralized pyroxenite, and 0.997 in overlying norite. In most samples in which sulfide and plagioclase coexist, the sulfide ²⁰⁷Pb/²⁰⁶Pb ratio is lower and ²⁰⁸Pb/²⁰⁶Pb ratio higher than the corresponding ones in plagioclase. For example, in a mineralized Merensky reef sample, average sulfide ²⁰⁷Pb/²⁰⁶Pb and ²⁰⁸Pb/²⁰⁶Pb ratios are 0.993 and 2.313, respectively, while those in plagioclase are 1.000 and 2.292. In one sample, the sulfide is extremely heterogeneous, with ²⁰⁷Pb/²⁰⁶Pb and ²⁰⁸Pb/²⁰⁶Pb ratios as low as 0.84 and 2.12. In this particular sample, the compositions must represent an isolated occurrence of addition of a young Pb component.The array of sulfide and plagioclase compositions requires multiple sources of Pb at the time of crystallization or soon thereafter. The disequilibrium between plagioclase and sulfide implies that some of the Pb originated from the isotopically distinct country rocks and was introduced at temperatures at which the composition of sulfide but not plagioclase could be modified. Thus, Bushveld sulfide, and to some extent plagioclase, do not reliably record the initial Pb isotopic composition(s) of the parent magma(s).     

Physical criteria for distinguishing sandy tsunami and storm deposits using modern examples

Modern subaerial sand beds deposited by major tsunamis and hurricanes were compared at trench, transect, and sub-regional spatial scales to evaluate which attributes are most useful for distinguishing the two types of deposits. Physical criteria that may be diagnostic include: sediment composition, textures and grading, types and organization of stratification, thickness, geometry, and landscape conformity.

Published reports of Pacific Ocean tsunami impacts and our field observations suggest that sandy tsunami deposits are generally < 25 cm thick, extend hundreds of meters inland from the beach, and fill microtopography but generally conform to the antecedent landscape. They commonly are a single homogeneous bed that is normally graded overall, or that consists of only a few thin layers. Mud intraclasts and mud laminae within the deposit are strong evidence of tsunami deposition. Twig orientation or other indicators of return flow during bed aggradation are also diagnostic of tsunami deposits. Sandy storm deposits tend to be > 30 cm thick, generally extend < 300 m from the beach, and will not advance beyond the antecedent macrotopography they are able to fill. They typically are composed of numerous subhorizontal planar laminae organized into multiple laminasets that are normally or inversely graded, they do not contain internal mud laminae and rarely contain mud intraclasts. Application of these distinguishing characteristics depends on their preservation potential and any deposit modifications that accompany burial.

The distinctions between tsunami and storm deposits are related to differences in the hydrodynamics and sediment-sorting processes during transport. Tsunami deposition results from a few high-velocity, long-period waves that entrain sediment from the shoreface, beach, and landward erosion zone. Tsunamis can have flow depths greater than 10 m, transport sediment primarily in suspension, and distribute the load over a broad region where sediment falls out of suspension when flow decelerates. In contrast, storm inundation generally is gradual and prolonged, consisting of many waves that erode beaches and dunes with no significant overland return flow until after the main flooding. Storm flow depths are commonly < 3 m, sediment is transported primarily as bed load by traction, and the load is deposited within a zone relatively close to the beach.     

Phase relations of pyroxene and amphibole in greenstone,blueschist and eclogite of the Franciscan Complex,California

The phase relations of pyroxenes, amphiboles and associated minerals in metamorphic rocks of the Franciscan Complex can be graphically depicted on a ternary diagram which has at its apices the metamorphic clinopyroxene end members, viz NaAl-NaFe³⁺-Ca(Fe²⁺, Mg). Phases are plotted by projection from a constant subassemblage of minerals. This analysis allows interpretation of the effects of pressure, temperature, bulk rock composition and fluid composition on stability of minerals within the Franciscan.Pyroxenes in meta-igneous rocks and metagraywackes have a limited compositional range and fall into two groups: the omphacites, with 50±5% diopside +hedenbergite component; and the jadeitic pyroxenes with 10±5% diopside+hedenbergite. Pyroxenes intermediate between these two groups are unstable relative to assemblages containing Na-amphibole+other minerals.Coexisting pyroxenes and amphiboles in eclogites and associated coarse blueschists comprise equilibrium assemblages, and the proportion of pyroxene to amphibole is a function of rock composition. Eclogites are stable at higher temperature than regionally developed fine-grained greenstones and blueschists in the Franciscan, and at higher pressure than amphibolites. X _H2O ^fluid is not an important factor in the stability of Franciscan eclogite relative to amphibolite.     

Petrology of andesites from the Yamato central rise,Sea of Japan

The composition of andesites from the Yamato central submarine rise and adjacent structures (Sea of Japan) points to the presence of a Late Cretaceous shortened and Oligocene-Miocene extended calc-alkaline series. With the general similarity of mineral assemblages of andesites, they are distinct in composition of minerals, which testifies to different formation conditions. The andesites of the extended type are the products of crystallization differentiation, whereas those of the shortened type are characterized by nonequilibrium composition of minerals, which reflects the heterogeneous primary melt, the composition of which discretely varied (probably repeatedly) during crystallization.     

Symplectites in upper mantle peridotites: Development and implications for the growth of subsolidus garnet,pyroxene and spinel

Silicate-oxide symplectites in complex mineral intergrowths are relatively common in upper mantle xenoliths and in xenoliths in the Jagersfontein Kimberlite, South Africa.Harzburgites of olivine and high-Al (1.9–3.6 wt%), Ca (0.6–0.9 wt%) and Cr (0.3–0.9 wt%) enstatite contain symplectites of spinel and diopside, or spinel, diopside and lower-Al (0.8–2.2 wt%), Ca (0.1–0.4 wt%) and Cr (0.02–0.8 wt%) enstatite. From textures and mineral chemistries these symplectites are interpreted to have formed by mineral unmixing and migration from Al–Ca–Cr discrete enstatite to adjoining mineral interfaces.Garnet harzburgites are composed of large (0.5–1 cm) olivine, equally large discrete low-Al (0.6–1.1 wt%), Ca (0.1–0.5 wt%), and Cr (0.1–0.3 wt%) enstatite and smaller interstitial garnet, diopside, and high-Cr and low-Al spinel. Symplectites are composed of either spinel+diopside+garnet, or garnet+spinel. Spinel diopside garnet symplectites have cores of spinel+diopside, resembling symplectites inharzburgites, but surrounded by rims of garnet or garnet+undigested globular spinel. From textures and chemistries we suggest that the spinel+diopside cores formed from Ca-Al-Cr-rich orthopyroxene initially as a nonstoichiometric homogeneous single phase clinopyroxene enriched in Fe, Cr and Al. This was followed by decomposition of the clinopyroxene to diopside+spinel, and subsequent garnet formation in a prograde reaction with olivine or enstatite. In bothharzburgites andgarnet harzburgites the metastable cellular structures may also have formed by the simultaneous precipitation of pyroxene and spinel. In all cases there is a strongly preferred embayment of symplectite bodies into olivine. Olivine appears to have activated adjacent     

Importance of heavy metal-organic matter interactions in natural waters

The role of organic ligands in metal complexing in natural waters has received little attention because of uncertainties regarding both the abundance and nature of dissolved organic carbon compounds. Recent data show that the bulk of dissolved organic matter in natural waters consists of highly oxidized and chemically and biologically stable polymeric compounds closely resembling soil humic substances. Average molar concentrations of these aquatic humics in major U.S. rivers range from 5 × 10^?6to 3 × 10^?5 moles 1^?1. Fractional elution of soil organic matter by meteoric waters may be considered to be the main process contributing to the presence of humic matter in rivers. The aquatic humic polymers participate in complex formation through ionizable functional groups with a range of differential acidities. The stabilities of metal-humic complexes in natural waters are higher than those of the corresponding inorganic metal complexes. Quantitative evaluation of the metal-organic interactions can be approached by applying variable equilibrium functions which take into account the differential physico-chemical characteristics of the active complexing sites on the polymer molecule. Assuming an average humic concentration of 10 mg 1^?1, complexation of trace metals can be significant even in the presence of excess concentrations of major cations.     

Platinum group minerals in podiform chromitites of the Bou Azzer ophiolite, Anti Atlas, Central Morocco

Summary The Neoproterozoic Bou Azzer ophiolite complex hosts numerous, small lenticular bodies of massive and disseminated chromite. Metallurgical-grade high-Mg and high-Cr spinels (cores with 48–62 wt% Cr₂O₃) reveal complex alteration patterns of successive Cr and Mn enrichment and loss of Al towards the rims, while the Mg# ratios [(Mg/(Mg + Fe²⁺)] remain almost constant. Concentration patterns of platinum-group elements are typical for ophiolitic chromitite poor in sulfides, with predominance of the IPGE, variable Rh, and low Pt and Pd. The most abundant platinum-group mineral is Rh-bearing laurite that occurs either included in spinel or in silicate matrix, whereas Os-Ir-Ru alloy is always included in spinel. Laurite inclusions reveal complex intergrowth textures with Rh-Ru-Pt rich alloy, and with Rh-rich sulfide. Most laurites display trends to sulfur-poor compositions leading to local formation of very fine-grained Ru-Os-Ir alloy phases. Ni-Co-Fe sulfides, arsenides and sulfarsenides devoid of PGE are associated with the alteration of chromite. Textural position and chemical composition of the base metal inclusions, as well as comparison of alteration features between chromite and accessory chromian spinel in the Co-Ni-As ores of the Bou Azzer ophiolite indicate a close connection. It is suggested that hydrothermal fluids percolated through the marginal zones of the ophiolite belt during greenschist facies metamorphism and deposited Ni-Co-Fe arsenides, sulfarsenides and minor sulfides as accessories within altered chromitites, and also in structurally favourable zones as Ni-Co-As ores. Author’s address: Dr. Frank Melcher, Federal Institute for Geosciences and Natural Resources, Stilleweg 2, 30655 Hannover, Germany     

Porphyroblast rotation during crenulation cleavage development: an example from the aureole of the Mooselookmeguntic pluton, Maine, USA

In the low‐pressure, high‐temperature metamorphic rocks of western Maine, USA, staurolite porphyroblasts grew at c. 400 Ma, very late during the regional orogenesis. These porphyroblasts, which preserve straight inclusion trails with small thin‐section‐scale variation in pitch, were subsequently involved in the strain and metamorphic aureole of the c. 370 Ma Mooselookmeguntic pluton. The aureole shows a progressive fabric intensity gradient from effectively zero emplacement‐related deformation at the outer edge of the aureole ～2900 m (map distance) from the pluton margin to the development of a pervasive emplacement‐related foliation adjacent to the pluton. The development of this pervasive foliation spanned all stages of crenulation cleavage development, which are preserved at different distances from the pluton. The spread of inclusion‐trail pitches in the staurolite porphyroblasts, as measured in two‐dimensional (2‐D) thin sections, increases nonlinearly from ～16° to 75° with increasing strain in the aureole. These data provide clear evidence for rotation of the staurolite porphyroblasts relative to one another and to the developing crenulation cleavage. The data spread is qualitatively modelled for both pure and simple shear, and both solutions match the data reasonably well. The spread of inclusion‐trail orientations (40–75°) in the moderately to highly strained rocks is similar to the spread reported in several previous studies. We consider it likely that the sample‐scale spread in these previous studies is also the result of porphyroblast rotation relative to one another. However, the average inclusion‐trail orientation for a single sample may, in at least some instances, reflect the original orientation of the overgrown foliation.     

Regional distribution of white K-mica polymorphs and their phengite content in the Central Alps

Some 150 white K-micas from the Central Alps were analysed for their polymorph and phengite content. Pre-Alpine white K-micas and those belonging to the Meso-Alpine Lepontine Metamorphic “High” show exclusively the 2M₁ polymorph. The 3T structural form, on the other hand, has been found in one third of the white K-micas formed during the Alpine regional metamorphism. In most cases this trigonal structure coexists with varying amounts of the 2M₁ form. The 3T distribution pattern suggests that this polymorph originated during the Eo-Alpine high-pressure/“low temperature” metamorphism. Provided this interpretation is correct, the sporadic occurrence of this polymorph within the Meso-Alpine staurolite zone may be used as a tracer for the Eo-Alpine metamorphism. The following improved correlation between the (060, 331) reflections of 2M₁ white K-micas and the RM-content (= 2Fe₂O₃+FeO+MgO in molar proportions), based on 24 micas from granitoid rocks, is presented: d(060, 331)= 1.498+0.082 RM. The phengite content of Alpine white K-micas belonging to the assemblage muscovite-biotite-K-feldspar-quartz was estimated from RM values or derived from chemical analyses and was found to be clearly related to metamorphic grade. Phengite-rich micas were formed during the Eo-Alpine high-P/“ low-T” metamorphism while aluminous muscovite was found within the Meso-Alpine thermal high of the Lepontine gneiss area. White K-micas from areas which underwent both the Eo-Alpine and the Meso-Alpine metamorphism display variable phengite contents. Although these micas show Tertiary Rb-Sr and K-Ar ages, the variable phengite content presumably reflects conditions during the Eo-Alpine high-P/“low-T” metamorphism. This interpretation implies that the cations occupying the interlayer positions are more easily equilibrated than those in octahedral and tetrahedral structural sites. A compilation of 3T white K-mica occurrences described in the literature is given in the appendix.     

Petrogenesis of Peraluminous Granites, Monashee Mountains, Southeastern Canadian Cordillera

Two-mica granites that locally contain garnet and sillimaniteoccur as dikes, sills, and sheets up to 50 m thick within thesillimanite zonc of the Monashee Mountains in the southeasternCanadian Cordillera of British Columbia. Syn-kinematic and post-kinematicgranites are recognized. U-Pb dating of zircon demonstrates that the syn-kinematic granitesare 100.4?0.3 Ma old, based on duplicate concordant single abradedzircon analyses. Other zircons have slightly older Pb/Pb dates,indicating small amounts of inherited zircons. Monazites are99?10 Ma old. Post-kinematic granites have 62.5?0.2 Ma zirconages and 634+0.1 Ma monazite ages. High initial 87 ratios (0.71492–0.74181)and evidence of Precambrian Pb inheritance indicates that bothsyn- and post-kinematic granites were derived from a crustalsource. Geobarometric estimates suggest that both generationsof granites equilibrated at 6–8 kb (22–30 km). Zirconand monazite saturation temperatures range from 660–824?Cand indicate that these minerals were liquidus phases earlyin the crystallization history of the granites. Because monazitesaturation temperatures generally exceed those of zircon, itis possible that some monazites may be inherited. Apatite saturationtemperatures in excess of 900?C suggest that both generationsof granites contain source inherited apatite. Syn- and post-kinematic granites have essentially identicalmajor and trace element chemistries. Syn-kinematic graniteshave steep light rare earth element (LREE) enriched patternswith pronounced negative Eu anomalies. The REE patterns of post-kinematicgranites range from steep LREE enriched patterns with negativeNd and Eu anomalies to flat patterns with low LREE contents,negative Nd anomalies, and both positive and negative Eu anomalies.Modelling of REE, Rb, Sr, and Ba contents demonstrates thatsyn-kinematic gramtes could have been generated by a low degreeof partial melting (with 10–25% feldspar fractionationof the melt) of Late Proterozoic Horsethief Creek Group metapelitesleaving a monazite-bearing upper amphibolite facies residue.Post-kinematic granites were produced by partial melting ofa geochemically and isotopically similar metapelitic source.The suite of post-kinematic granites can be related by a smallamount (up to 0.1%) of monazite crystal fractionation.