Dissolved air flotation (DAF) of fine quartz particles using an amine as collector

Experimental studies concerning the dissolved air flotation (DAF) of fine (d_p < 100 μm) quartz particles, using two different flotation cells (setups), are presented. Pure and well characterised quartz samples were treated with a commercial amine as collector prior to flotation and bubbles were characterised by the LTM-BSizer technique. Bubble size distribution showed 71% (by volume) and 94% (by number) of the bubbles having sizes (d_b) lower than 100 μm (i.e. microbubbles). The Sauter and arithmetic mean diameters were 79 μm and 56 μm, respectively, for the bubbles generated at 300 kPa (gauge) saturation pressure (after 30 minute saturation time). Quartz particle size distribution (obtained by laser diffraction) showed a volume-moment diameter of 13 μm. The Rosin–Rammler–Bennett, Gates–Gaudin–Schumann and log-normal distribution functions were well fitted (R² > 0.96) to the bubble size distribution and quartz particle size distribution data. Values of total quartz recovery ranging from 6% to 53% (by mass) were obtained for the DAF experiments under different collector concentrations (up to 2 mg g^− 1), with an optimal collector concentration found at 1 mg g^− 1. These results are significant considering that 27% (by volume) of the quartz particles are ultrafine (d_p < 5 μm), demonstrating the widely-known efficiency of DAF to remove small particles when applied in the field of water and wastewater treatment. The true flotation behaviour, as a function of particle diameter (d_p), exhibits a local minimum when particles are approximately 3–5 μm in size. The results contribute to the discussion in the literature about the existence of such a minimum, which is generally interpreted as a change in the mechanism of particle collection from convection (collision) to diffusion at lower particle sizes.     

Distribution and dispersion of gold in point bar and pavement sediments of the Huai Hin Laep, Loei, northeastern Thailand

Gold anomalies in drainage sediments are often erratic, reflecting both the nugget effect and hydraulic effects whereby gold is concentrated at favorable sites along a stream. This study investigates these factors in a stream in northeastern Thailand.Bulk sediment samples, consisting of approximately 40 kg of −12 mm material, were collected from bar and pavement sites along an 8 km study reach. Samples were wet sieved into eight size fractions. The five fractions between 425 μm and 53 μm were then processed to obtain heavy mineral concentrates (SG > 3.3). Gold content of all size and density fractions finer than 425 μm was determined by fire assay-atomic absorption.Concentrations of Au in the heavy mineral concentrates typically range from 10,000 to 50,000 ppb (maximum 198,000 ppb), whereas the corresponding light mineral fractions and the −53 μm fraction generally contain <5 ppb gold. Within the heavy mineral fractions concentrations of Au generally increase downstream away from their supposed source and are higher at pavement than at point bar sites. Variations in abundance of gold between point bar sites can be related to stream characteristics (such as width, velocity and bed roughness) that are indicative of changing energy conditions and of the ability of the stream to winnow light minerals from its bed.The estimated median number of gold particles in the heavy mineral concentrates increase from less than one in the 212–425 μm fraction to about three in the 53–106 μm size range. However, because of dilution by the light mineral and −53 μm fractions, the probability of a 30 g analytical sub-sample containing a particle of gold is so low that in thirteen out of sixteen −149 μm sediment samples no gold was detected. Insofar as this results from dilution by large quantities of −53 μm sediment, failure of conventional sieved sediment samples to reliably detect the anomaly is probably a consequence of increased erosion caused by deforestation and land usage.Heavy mineral concentrates from pavement and other high energy sites are more reliable than conventional sediment samples for detecting gold anomalies of the Huai Hin Laep type. A low sample density is adequate but, because anomaly contrast may increase downstream, careful interpretation is required.     

Transport of trace elements under different seasonal conditions: Effects on the quality of river water in a Mediterranean area

Concentrations of total and dissolved elements were determined in 35 water samples collected from rivers in Sardinia, a Mediterranean island in Italy. The overall composition did not change for waters sampled in both winter and summer (i.e., January at high-flow condition and June at low-flow condition), but the salinity and concentrations of the major ions increased in summer. Concentrations of elements such as Li, B, Mn, Rb, Sr, Mo, Ba and U were higher in summer with only small differences between total and dissolved (i.e., in the fraction <0.4 μm) concentrations. The fact that these elements are mostly dissolved during low flow periods appears to be related to the intensity of water–rock interaction processes that are enhanced when the contribution of rainwater to the rivers is low, that is during low-flow conditions. In contrast, the concentrations of Al and Fe were higher in winter during high flow with total concentrations significantly higher than dissolved concentrations, indicating that the total amount depends on the amount of suspended matter. In waters filtered through 0.015 μm pore-size filters, the concentrations of Al and Fe were much lower than in waters filtered through 0.4 μm pore-size filters, indicating that the dissolved fraction comprises very fine particles or colloids. Also, Co, Ni, Cu, Zn, Cd and Pb were generally higher in waters collected during the high-flow condition, with much lower concentrations in 0.015 μm pore-size filtered waters; this suggests aqueous transport via adsorption onto very fine particles. The rare earth elements (REE) and Th dissolved in the river waters display a wide range in concentrations (∑REE: 0.1–23 μg/L; Th: <0.005–0.58 μg/L). Higher REE and Th concentrations occurred at high flow. The positive correlation between ∑REE and Fe suggests that the REE are associated with very fine particles (>0.015 and <0.4 μm); the abundance of these particles in the river controls the partitioning of REE between solution and solid phases.Twenty percent of the water samples had dissolved Pb and total Hg concentrations that exceeded the Italian guidelines for drinking water (>10 μg/L Pb and >1 μg/L Hg). The highest concentrations of these heavy metals were observed at high-flow conditions and they were likely due to the weathering of mine wastes and to uncontrolled urban wastes discharged into the rivers.     

Distribution and behavior of gold in soils and tills at the Nickel Plate Mine, southern British Columbia, Canada

The Nickel Plate deposit, in which gold occurs as <25 μm blebs associated with arsenopyrite in garnet-pyroxene skarns, is in the subalpine zone near the southern limit of the Thompson Plateau. During the last glaciation the Cordilleran ice sheet moved south-southwest across the deposit and deposited a stony basal till. A dispersion train with anomalous concentrations of gold in tills and soils now extends 2 km down ice from the deposit.Gold contents of samples of humus (LFH horizon) and the −212 μm fraction of mineral soils (A, B and C horizons) was determined by instrumental neutron activation and fire assay-atomic absorption, respectively. Selected samples were examined in detail to determine distribution of gold between different size and density fractions.Despite erratic variability, Au contents of the −212 μm fraction generally decrease from 200–400 ppb close to the mine site to <50 ppb at distal sites. At most sites there is also a twofold increase of gold values down the soil profile. Within samples concentrations of Au in the −420 + 212 μm, −212 + 106 μm, −106 + 53 μm and −53 μm fractions are usually roughly constant. However, because of its abundance, the −53 μm fraction contains more than 70% of the gold. Amenability of gold in this fraction to cyanidation suggests that it is largely free gold. For size fractions > 53 μm the contribution of the heavy mineral (SG > 3.3) fraction to total gold content increases with decreasing grain size.Distribution of gold between size and density fractions is consistent with its release from the bedrock or pre-glacial regolith by glacial abrasion. The bulk of the gold was incorporated into the fine fractions of the till at or close to the source. However, differences between down ice dilution ratios for gold in different heavy mineral size fractions suggest that comminution of host minerals continued to transfer gold to the finer size fractions during glacial transport.For exploration purposes, B and C horizon samples provide the best anomaly contrast. Estimates of the abundance of gold particles in different size fractions indicate that the nugget effect, which causes erratic gold values in the −212 μm fraction, can be avoided by analysis of 30 g of −53 μm material.     

Lignin is preserved in the fine silt fraction of an arable Luvisol

Knowledge about the fate of individual biomolecules during the decomposition process in soil is limited. We used the natural isotopic label introduced by 23 years of continuous maize cropping, together with compound specific ¹³C isotope analysis, to study lignin monomers in particle size fractions of a Luvisol. Isotope data indicated apparent decadal turnover times for lignin. A kinetic model suggests the existence of a fast and a slow decomposing lignin pool in the soil, reconciling a low stock-to-input ratio with decadal turnover times. We found new, maize-derived lignin primarily in the 63–2000 μm fraction, whereas old, C₃-derived lignin from the pre-maize vegetation had accumulated mainly in the silt (2–20 μm) fraction. This distribution of lignin differed from that of total organic carbon, which was concentrated in the <2 μm fraction. Old, C₃-derived carbon in all the soil fractions was depleted in lignin compared to new, maize-derived carbon. The observation that the 2–20 μm fraction was less depleted than the others indicates that lignin preservation is particle size specific, but the underlying mechanism controlling its preservation is not clear.     

Application of in vitro extraction studies to evaluate element bioaccessibility in soils from a transect across the United States and Canada

In vitro bioaccessibility tests (IVBA) are inexpensive, physiologically-based extraction tests designed to estimate the bioaccessibility of elements along ingestion exposure pathways. Published IVBA protocols call for the testing to be done on the <250-μm fraction of soil, as these particles are most likely to adhere to the hands of children and be ingested. Most IVBA in the literature to date have been applied to soil samples from highly contaminated sites or to spiked samples, and relatively little work has been done to evaluate bioaccessibility of elements in a wide variety of uncontaminated ‘background’ soils.In 2004, the US Geological Survey and the Geological Survey of Canada sampled soils along north–south and east–west transects across the two countries to test and refine sampling and analytical protocols recommended for the planned soil geochemical survey of North America. Samples were collected at 220 sites selected randomly at approximately 40-km intervals. The focus of the investigation presented in this paper was twofold: (1) to begin to examine variations in bioaccessibility of As, Cd, Cr, Ni and Pb in a number of ‘background’ (i.e., unpolluted) soils from around North America and (2) to determine if there are significant differences that would preclude using the standard size fraction of <2 mm for extraction with a simulated gastric fluid as an expeditious and inexpensive bioaccessibility screening tool for the large numbers of future samples to be collected by this continental-scale project. A subset of 20 soil samples collected along the north–south transect at a depth of 0–5 cm was used for this study. Two separate size fractions (<2 mm and <250 μm) were extracted using a simulated human gastric fluid consisting of a solution of HCl and glycine adjusted to a pH of 1.5. In general, the leachate results for the <2-mm size fraction were not substantially different than those for the <250-μm size fraction for concentrations of As, Cd, Cr, Ni and Pb. Leachate concentrations for Cd, Ni and Pb appear to be controlled to some extent by the total concentration of the element in soil. Bioaccessibility of the elements in this study decreased in the order, Cd > Pb > Ni > As > Cr.     

A study on the preparation of fine and low soda alumina

A simple process to produce fine and low soda α-alumina (α-Al₂O₃) from a commercial grade aluminium trihydroxide (gibbsite, Al(OH)₃) produced by KC Corporation Ltd was developed. There are two options for this process with the first one producing low soda α-alumina (< 0.05% Na₂O) having a mean particle size of 50 μm. The second option yields a fine product with a mean size of less than 10 μm. In the first option, a plant aluminium trihydroxide containing 0.20% Na₂O was first fluidized with nitrogen at 400–600 °C to yield an amorphous activated alumina. This intermediate product was then treated with acetic or oxalic acid, washed with water and heated to 1200 °C to form calcined α-alumina, having a Na₂O content of less than 0.05%. A 20 min leaching using 0.2 M acetic or oxalic acid could yield an alumina product containing 0.04% Na₂O. In the second option, a new technique for the preparation of fine and low soda α-alumina was evaluated using an attrition mill working also as a leaching vessel at 80 °C. Fine (< 10 μm in mean particle size) and low soda (< 0.04% Na₂O) alumina was produced by a 20 min leaching step with 0.2 M acetic acid and concurrent attrition milling.     

Size distribution of gold in some soils associated with selected gold mineralization in Canada and the United States of America

Samples were collected near known gold mineralization from anomalous and background soils developed on glacial till in British Columbia and Ontario, and in residual soils in Nevada, Utah and the Yukon Territory. After wet sieving to five size fractions finer than 2000 mm, and separation of heavy minerals (S.G. > 3.3) for the − 212 + 106 μm and − 106 + 53 μm fractions, gold concentrations in each fraction were determined by fire assay-atomic absorption.In all cases more than 60% of the gold resides in the − 53 μm fraction. For the residual soils most of the remaining gold is associated with the light mineral fractions and only a negligible proportion resides in the heavy minerals. Estimates of the numbers of gold particles and subsampling variability suggest that gold, in both heavy and light mineral fractions, is largely present as inclusions of fine gold. For exploration purposes, optimum sample representativity would be obtained with the − 53 μm fraction. However, because this fraction is a major component of the soils, use of a coarser size fraction (e.g., − 212 μm) will only slightly reduce sample representativity. Also, because most of the gold is associated with the − 53 μm and light mineral fractions, use of heavy mineral concentrates offers no significant advantage and in some cases would result in anomalous conditions being overlooked.     

A preliminary study on the enrichment mechanism and occurrence of hazardous trace elements in the Tertiary lignite from the Shenbei coalfield, China

The Cr and Ni contents are high in the Eocene lignite of the Shenbei coalfield, which is a small intracontinental basin located in Liaoning Province, China. In this paper, we studied the distribution, origin and occurrence of Cr, Ni and other hazardous trace elements in the Shenbei lignite on the basis of coal petrology, and geochemistry of the lignite and combustion products. The following conclusions on the Shenbei lignite can be drawn: (1) The dominant maceral group in the Shenbei coal is huminite (humodetrinite), accounting for 96%–99% of the total maceral. Inertinite content is less than 1%. Liptinite content (sporinite and cutinite) is 0.2–1.6%. Common minerals in the Shenbei lignite include clay minerals (kaolinite), pyrite and quartz, and calcite and siderite. Chromite is not present in the lignite. (2) Potentially hazardous trace elements such as Co (22 μg/g), Cr (79 μg/g), Cu (63 μg/g), Zn (93 μg/g), V (88 μg/g) and Ni (75 μg/g) are strongly enriched in the Shenbei lignite compared with average concentration of trace elements in the Chinese coal and worldwide lignite. These elements are mainly associated with fulvic acid (FA) and/or coal organic macromolecular compounds in most of the studied lignite samples, indicating an organic association and enrichment of these elements in the Shenbei lignite. (3) Unusually high trace elements contents in the Shenbei lignite are derived mainly from the olivine basalt (country rock of coal basin) that consists of 52.7% plagioclase, 17.8% pyroxene, 14% olivine and 15.5% Ti–Fe oxide minerals. These olivine basalts have higher Cr, Ni, Pb and Zn contents than other types of rock and worldwide basalts do. (4) Fly ash of the Shenbei lignite, with 90% 1–50 μm amorphous particles and 8% 1–10 μm cenosphere, has high contents of Zn (23,707 μg/g), Be (12 μg/g), Sr (1574 μg/g), Pb (486 μg/g) and Cr (349 μg/g). In particular, the ferruginous micro-cenoshperes contain 1–12.79% Zn. Fine bottom ash (<0.031mm) of the Shenbei lignite has higher contents for most of the elements with the exception of Mo, Sn and Zn. Therefore, the potentially environmental and health impact of the fly ash and fine bottom ash should constitute a major concern.     

Fractal distribution of particle size in carbonate cataclastic rocks from the core of a regional strike-slip fault zone

We present particle size data from 31 samples of carbonate cataclastic rocks collected across the 26 m thick fault core of the Mattinata Fault in the foreland of the Southern Apennines, Italy. Particle size distributions of incoherent samples were determined by a sieving-and-weighting technique. The number of weight-equivalent spherical particles by size is well fitted by a power-law function on a log–log space. Fractal dimensions (D) of particle size distributions are in the 2.091–2.932 range and cluster around the value of 2.5. High D-values pertain to gouge in shear bands reworking the bulk cataclastic rocks of the fault core. Low D-values characterise immature cataclastic breccias. Intermediate D-values are typical of the bulk fault core. Analysis of the ratio between corresponding equivalent particle numbers from differently evolved cataclastic rocks indicates that the development of particle size distributions with D>2.6–2.7 occurred by a preferential relative increase of fine particles rather than a selective decrement of coarse particles. This preferentially occurred in shear bands where intense comminution enhanced by slip localisation progressed by rolling of coarse particles whose consequent smoothing produced a large number of fine particles. Our data suggest that during the progression of cataclasis, the fragmentation mode changed from the Allègre et al.'s [Nature 297 (1982) 47] “pillar of strength” mechanism in the early evolutionary stages, to the Sammis et al.'s [Pure and Applied Geophysics 125 (1987) 777] “constrained comminution” mechanism in the subsequent stages of cataclasis. Eventually, localised shear bands developed mainly by abrasion of coarse particles.     

The effects of surface area, grain size and mineralogy on organic matter sedimentation and preservation across the modern Squamish Delta, British Columbia: the potential role of sediment surface area in the formation of petroleum source rocks

Surface sediment samples were collected from the Squamish River Delta, British Columbia, in order to determine the role of sediment surface area in the preservation of organic matter (OM) in a paralic sedimentary environment. The Squamish Delta is an actively prograding delta, located at the head of Howe Sound.Bulk total organic carbon (TOC) values across the Squamish Delta are low, ranging from 0.1 to 1.0 wt.%. The carbon/total nitrogen ratio (C_org/N) ranges from 6 to 17, which is attributed to changes in OM type and facies variations. The <25-μm fraction has TOC concentrations up to 2.0 wt.%, and a C_org/N ratio that ranges from 14 to 16. The 53–106-μm fraction has higher TOC concentrations and C_org/N ratios relative to the 25–53-μm fraction. The C_org/N ratio ranges from 9 to 18 in the 53–106-μm fraction and 5.5–10.5 in the 25–53-μm fraction. Surface area values for bulk sediments are low (0.5–3.0 m²/g) due to the large proportion of silt size material. Good correlation between surface area and TOC in bulk samples suggests that OM is adsorbed to mineral surfaces. Similar relationships between surface area and TOC were observed in size-fractionated samples. Mineralogy and elemental composition did not correlate with TOC concentration.The relationships between surface area, TOC and total nitrogen (TN) can be linked to the hydrodynamic and sedimentological conditions of the Squamish Delta. As a result, the Squamish Delta is a useful modern analogue for the formation of petroleum source rocks in ancient deltaic environments, where TOC concentrations are often significantly lower than those in source rocks formed in other geological settings.     

Carbon isotope fractionation in phospholipid fatty acid biomarkers of bacteria and fungi native to an acid mine drainage lake

This study identifies isotope signatures associated with autotrophic and heterotrophic microbial communities that may provide a means to determine carbon cycling relationships in situ for acid mine drainage (AMD) sites. Stable carbon isotope ratios (δ¹³C) of carbon sources, bulk cells, and membrane phospholipids (PLFA) were measured for autotrophic and heterotrophic microbial enrichment cultures from a mine tailings impoundment in northern Ontario, Canada, and for pure strains of the sulfur oxidizing bacteria Acidithiobacillus ferrooxidans and Acidithiobacillus thiooxidans. The autotrophic enrichments had indistinguishable PLFA distributions from the pure cultures, and the PLFA cyc-C_19:0 was determined to be a unique biomarker in this system for these sulfur oxidizing bacteria. The PLFA distributions produced by the heterotrophic enrichments were distinct from the autotrophic distributions and the C_18:2 PLFA was identified as a biomarker for these heterotrophic enrichments. Genetic analysis (16S, 18S rRNA) of the heterotrophic cultures indicated that these communities were primarily composed of Acremonium fungi.Stable carbon isotope analysis revealed that bulk cellular material in all autotrophic cultures was depleted in δ¹³C by 5.6–10.9‰ relative to their atmospheric CO₂ derived carbon source, suggesting that inorganic carbon fixation in these cultures is carbon limited. Individual PLFA from these autotrophs were further depleted by 8.2–14.6‰ compared to the bulk cell δ¹³C, which are among the largest biosynthetic isotope fractionation factors between bulk cell and PLFA reported in the literature. In contrast, the heterotrophic bulk cells were not significantly fractionated in δ¹³C relative to their carbon source and heterotrophic PLFA ranged from 3‰ enriched to 4‰ depleted relative to the isotopic composition of their total biomass. These distinct PLFA biomarkers and isotopic fractionations associated with autotrophic and heterotrophic activity in this laboratory study provide potential biomarkers for delineating autotrophic and heterotrophic carbon cycling in AMD environments.     

Refractory organic carbon in particle-size fractions of arable soils I: distribution of refractory carbon between the size fractions

Refractory compounds are responsible for the long-term sequestration of organic matter in soil. The aim of this study is to assess the storage of refractory compounds, i.e. compounds with long turnover times, across size separates in arable soils. The contents and distribution of organic carbon (OC) and nitrogen (N) in size fractions were examined for two contrasting treatment types from long-term agroecosystem experiments, i.e. C-depleted and fertilized plots. The soil organic carbon (SOC) pool of the C-depleted plots is considered to be relatively enriched in refractory compounds compared with the SOC in the fertilized counterparts. In two of the three long-term experiments, the relative retention of OC in separates <20 μm was considerably higher than in separates 2000–20 μm (OC contents in depleted plots compared with fertilized plots). Highest residual contents of OC were found in fractions <6 μm. In the third experiment, additionally to the very fine fractions, separates 250–20 μm retained a high proportion of OC. The behavior of N was analogous to that of OC: the highest relative residues in the depleted plots were found in fine separates. These results indicate that in the investigated arable soils, C and N compounds associated with fine separates are most stable. Refractory OC in arable soils may be largely stored in fine particle-size fractions.     

Organic geochemistry and petrology of barren and Mo–Ni–PGE mineralized marine black shales of the Lower Cambrian Niutitang Formation (South China)

Marine black shales of the Lower Cambrian Niutitang Formation in southern China host Mo–Ni–platinum group elements (PGE) mineralization confined to a phosphate- and pyrite-rich stratiform body (max. 20-cm thick). The H/C atomic ratio, carbon isotopic composition, FTIR spectra of bulk organic matter, and spectra of extractable part of organic matter indicate similar sources and thermal evolution of organic matter in barren and mineralized black shales.The morphology and relative abundance of organic particles in barren and mineralized shales are different. In barren black shales, organic particles comprise only elongated bodies and laminae 2–10 μm across or elongated larger bodies (> 10 μm) with R_max = 2.96–5.21% (Type I particles). Mineralized black shales contain Type I particles in rock matrix (90–95 vol%), small veinlets or irregular organic accumulations (Type II particles, 1–5 vol%) that display weak to well developed mosaic texture and a variable reflectance (R_max = 3.55–8.65%), and small (< 1 to 5 μm) rounded or irregular Type III organic particles (1–4 vol%) distributed within phosphate nodules and sulphide rip-up clasts. Type III particles show similar reflectance as particles of Type I in rock matrix. Type I particles are interpreted as remnants of in situ bacterially reworked organic matter of cyanobacteria/algal type, Type II as solidified products or oil-derived material (migrabitumen), and Type III particles as remnants of original organic matter in phosphatized or sulphidized algal/microbial oncolite-like bodies. Equivalent vitrinite reflectances of Type I and III particles in barren and mineralized rocks are similar and correspond to semi-anthracite and anthracite. Micro-Raman spectra of organic particles in rocks display a wide belt in the area of 1600 cm^− 1 (G belt) and approximately the same belt in the area of 1350 cm^− 1 (D belt). The ratio of integrated areas of the two belts correlate with R_max values.The Mo–Ni–PGE mineralized body is interpreted as to represent a remnant of phosphate- and sulphide-rich subaquatic hardground supplied with organic material derived from plankton and benthic communities as well as with algal/microbial oncolite-like bodies that originated in wave-agitated, shallow-water, nearshore environment.     

The use of the fine fractions of stream sediments in geochemical exploration in arid and semi-arid terrains

Partitioning of Cu, Pb, Zn, U, As and Mo between the minus 70 μm and minus 200 μm fractions of stream sediments from arid and semi-arid terrains is examined in the light of published case histories supplemented by new data. The advantages of selecting a particular fraction for routine sampling in such arid environments are assessed in terms of five criteria: (1) homogeneity of background population; (2) definition of threshold; (3) absolute element abundance levels; (4) contrast between anomalous and background populations; and (5) length of dispersion train. The most homogeneous background population distributions and improved definition of the threshold between background and anomaly occur in the very fine, minus 70 μm fraction of stream sediments for the majority of elements, in particular for Zn, Cu, U and As. Data for Pb and Mo do not consistently favour either size fraction in the case histories studied. Increased abundance levels of elements which are normally close to the analytical detection limit (U, Mo, As) occur most frequently in the minus 70 μm fraction, although Cu, Pb and Zn levels are commonly higher in the coarser fraction. In addition the finer size fraction better defines the anomalous population and provides the longer dispersion trains for Cu, Pb, Zn, U and As in the majority of case histories.The data examined indicate that the minus 70 μm fraction provides more useful information, in many instances, than the minus 200 μm fraction. The evidence suggests that problems expected with the use of the fine fraction — dilution through the abundance of wind blown material, and insufficient fine sediment — do not restrict the use of this fraction in stream sediment surveys in arid terrains.     

Traceurs sédimentaires des variations du niveau marin et de la mousson sud-est asiatique depuis 450 ka en mer de Chine du Sud

In order to reconstruct the past variations of the Southeast Asian monsoon intensity and estimate the sedimentary system reactivity to climatic changes in Southeast Asia over the last 450 kyr, mineralogical and sedimentological analyses have been performed on the terrigenous fraction of the South China Sea sediment. End-member modelling coupled with grain size data discriminates three end-members that determine the nature and intensity of the main sediment transport vectors. Low sea-level stands are characterized by sediment reworking that allows transportation of a coarse end-member (20–40 μm) to the deep-basin. By contrast, the other end-members (4–6 μm; 9–13 μm) are controlled by the shoreline position (sea level) and/or by changes of the rivers capacity transport (monsoon). Finally, aeolian input to the northern margin of the South China Sea can be considered negligible compared to the massive fluvial input and the reworking of the sediments.     

Organic geochemistry of Recent equatorial deltaic sediments

The organic matter of recent deltaic sediments cored in the Mahakam delta, East Kalimantan, has been studied before and after physical fractionation into sands >50 μm, silts 5–50 μm and clays <5 μm. Both the lipid and non-lipid components have been investigated.Weight, carbon and nitrogen fractionation budgets were used to define three types of samples, depending on coarse particle contributions to the total amount of organic matter: a = a first type with more than 50% of the O.M. in the coarse particles, high C/N ratios and O.M. content, b = an intermediary type with medium C/N ratios and O.M. content, each fraction having quite the same O.M. content, c = a third type with less than 5% of the whole O.M. in the sands and the lowest C/N ratios and O.M. content.Concerning the global organic characteristics of the fractions, a systematic increase of C/N ratios occurs when going from clays to sands; the finer the fraction is, the more nitrogenous the compounds are. This enrichment in nitrogen is related to a persistent high rate of hydrolysable material either for argillaceous organic matter-poor sediments or for the clay fractions of all types of samples. Conversely, the type (a) coarse sediments, in particular the sandy components were resistant to acid hydrolysis with burial.Concerning the geochemical markers signatures of granulometric fractions, the distribution patterns of n-alkanes and n-fatty acids are characterized by the predominance of high molecular weight compounds >C₂₂. Carbon preference index (CPI) values are higher in the sands and silts, reflecting their enrichment in continentally-derived vegetation debris. For type (c), the fractionation revealed markers of microbial activity within the clay fractions. For all types of samples, we observed an increase with burial of the n-alkane and n-fatty acid concentrations, particularly in the clay fractions, suggesting possibly a better preservation and/or affinity of lipids with the finest fractions.     

Groundwater helium surveys in mineral exploration in Australia

The potential for using groundwater helium surveys in exploration has been evaluated by conducting local and regional surveys in several mineralized and background areas in Australia. Dissolved helium contents decrease markedly upwards, particularly in the top 10–15m, due to degassing in attaining dynamic equilibrium with the atmosphere. Gradients of depth profiles are not uniform but because total concentration variations to 50m or more are commonly less than 10, whereas regional variations are 10³–10⁵, samples from the greatest constant depth possible below water-table are adequate for survey purposes. Helium concentrations in excess of the atmosphere equilibrium value of 0.044 μl He/l H₂O were found to be associated with uranium mineralization at Honeymoon (6.9–44.4 μl/l), Manyingee (0.08–1.68 μl/l), Bennett Well (9.9–29.5 μ/l) and the Stuart Shelf—Roxby Downs (910–2495 μl/l), with a carbonatite at Mt. Weld (0.18–13.6 μl/l), and with kimberlites at Wandagee (0.2–3.25 μl/l). No anomaly was associated with the shallow calcrete uranium deposit at Yeelirrie. However, equivalent or higher concentrations were found in groundwaters from unmineralized areas around these deposits, e.g. up to 85 μl/l at Manyingee—Bennett Well, to 215 μl/l at Yeelirrie and to 1525 μl/l, Stuart Shelf—Mt. Gunson. Similarly, helium in waters from stock wells near Mt. Weld appears to indicate the presence of the carbonatite but in a survey of a geologically similar area near Malcolm, equivalent anomalies were not related to carbonatite.Although the uranium (and thorium) mineralization is a significant source, high helium concentrations can arise by accumulation in groundwaters with long residence times and by leakage from deep sources, particularly granitoid basement. The concentration reached is also a function of the porosity and configuration of the aquifer and the permeability of the aquiclude to helium. These factors are more important in determining dissolved helium concentrations than the uranium and thorium contents of the rocks. However, the effects are not readily quantifiable, particularly in exploration areas where geology and hydrology are relatively unknown, hence helium groundwater data can be difficult if not impossible to interpret.     

K–Ar dating of fault gouge in the northern Sydney Basin, NSW, Australia—implications for the breakup of Gondwana

The occurrence of synkinematic and authigenic clay minerals is a common feature in fault gouges. Few attempts have been made to date fault gouges. We present the first age data in Australia for synkinematic illite–smectite growth in two fault zones of the northern Sydney Basin, NSW. The faults occur at Burwood Beach, NSW in the northern part of the Sydney Basin and are hosted by Early Permian siltstones, tuffs and coals of the Lambton Formation, Newcastle Coal Measures. The faults are 1.5 m apart, show normal displacement and trend N–S with steep easterly dips. Foliated gouge zones, comminution and dilational breccias are developed along both fault surfaces. K–Ar ages extracted from samples in the gouge and tuffs in the damage zones are 172 (6–10 μm) to 119 Ma (<0.4 μm), respectively. Older ages of 272–281 Ma for the coarse fractions (>2 μm), 237–245 Ma for the <2 μm fraction, 218 Ma for the <0.4 μm fraction and 196 Ma for the <0.1 μm fraction have been obtained from siltstones within and outside the damage zone. We believe the younger ages of 196–237 Ma indicate the time at which diagenetic illite–smectite formed and the 122–150 Ma dates from the <2 μm fraction represent the maximum age of gouge formation. The younger ages are thought to reflect the last slip event occurring on the faults, which is related to the rifting and dispersal of the eastern margin of the Australian continent.     

Mineralogy and petrology of Al-rich objects and amoeboid olivine aggregates in the CH carbonaceous chondrite North West Africa 739

The aluminum-rich (>10 wt% Al₂O₃) objects in the CH carbonaceous chondrite North West Africa (NWA) 739 include Ca,Al-rich inclusions (CAIs), Al-rich chondrules, and isolated mineral grains (spinel, plagioclase, glass). Based on the major mineralogy, 54 refractory inclusions found in about 1 cm² polished section of NWA 739 can be divided into hibonite-rich (16%), grossite-rich (26%), melilite-rich (28%), spinel-pyroxene-rich (16%) CAIs, and amoeboid olivine aggregates, (AOA's, 17%). Most CAIs are rounded, 25–185 μm (average=70 μm) in apparent diameter, contain abundant, tiny perovskite grains, and typically surrounded by a single- or double-layered rim composed of melilite and/or Al-diopside; occasionally, layers of spinel+hibonite and forsterite are observed. The AOAs are irregularly shaped, 100–250 μm (average=175 μm) in size, and consist of forsterite, Fe,Ni-metal, and CAIs composed of Al-diopside, anorthite, and minor spinel. One AOA contains compact, rounded melilite-spinel-perovskite CAIs and low-Ca pyroxene replacing forsterite. The Al-rich (>10 wt% bulk Al₂O₃) chondrules are divided into Al-diopside-rich and plagioclase-rich. The Al-diopside-rich chondrules, 50–310 μm (average=165 μm) in apparent diameter, consist of Al-diopside, skeletal forsterite, spinel, ±Al-rich low-Ca pyroxene, and ±mesostasis. The plagioclase-rich chondrules, 120–455 μm (average=285 μm) in apparent diameter, are composed of low-Ca and high-Ca pyroxenes, forsterite, anorthitic plagioclase, Fe,Ni-metal nodules, and mesostasis. The isolated spinel occurs as coarse, 50–125 μm in size, subhedral grains, which are probably the fragments of Al-diopside chondrules. The isolated plagioclase grains are too coarse (60–120 μm) to have been produced by disintegration of chondrules or CAIs; they range in composition from nearly pure anorthite to nearly pure albite; their origin is unclear. The Al-rich objects show no evidence for Fe-alkali metasomatic or aqueous alteration; the only exception is an Al-rich chondrule fragment with anorthite replaced by nepheline. They are texturally and mineralogically similar to those in other CH chondrites studied (Acfer 182, ALH85085, PAT91467, NWA 770), but are distinct from the Al-rich objects in other chondrite groups (CM, CO, CR, CV). The CH CAIs are dominated by very refractory minerals, such as hibonite, grossite, perovskite and gehlenitic melilite, and appear to have experienced very low degrees of high-temperature alteration reactions. These include replacement of grossite by melilite, of melilite by anorthite, diopside, and spinel, and of forsterite by low-Ca pyroxene. Only a few CAIs show evidence for melting and multilayered Wark-Lovering rims. These observations may suggest that CH CAIs experienced rather simple formation history and escaped extensive recycling. In order to preserve the high-temperature mineral assemblages, they must have been efficiently isolated from the hot nebular region, like some chondrules and the zoned Fe,Ni-metal grains in CH chondrites.