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1.
This review paper presents the results of an extensive study investigating whether addition of 3% w/w Greek lignite to 6.42% w/w water–bentonite suspensions, after being exposed to high temperatures, can prevent gelation and control filtration characteristics. Two different bentonites and eight lignites from different Greek basins have been used while a commercial lignite product has been used as standard. The lignite-free bentonite suspensions heated to 177 °C for 16 h (thermal aging) thicken considerably, increasing the yield stress and the yield point. Fluid consistency and flow behavior indices also change while no significant change is observed for plastic viscosity. Thermal aging of the suspensions results in unacceptably high fluid loss values.Addition of Greek lignite to water–bentonite suspensions, followed by thermal aging, provided the rheological stability of the suspensions by maintaining the low yield stress/point regardless of the type of bentonite. Some of the lignites performed as well as their commercial counterpart. No specific trends for rheological improvement have been identified with respect to various characteristics of lignites such as contents of humic, fulvic acids, humins and other parameters such as specific surface area and cation exchange capacity.Furthermore, addition of lignite in most cases provided very good filtration control of the water–bentonite suspensions after exposure to 177 °C, with some Greek lignites being superior to the commercial product. The same lignite parameters examined for rheological control, were also examined to determine their effect on fluid loss of these suspensions for both bentonites. The content of humic and fulvic acids of two groups of lignites showed weak inverse correlations with the fluid loss volumes for both bentonites, while all other parameters did not seem to directly correlate with the effectiveness of the lignites.  相似文献   

2.
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 (Corg/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 Corg/N ratio that ranges from 14 to 16. The 53–106-μm fraction has higher TOC concentrations and Corg/N ratios relative to the 25–53-μm fraction. The Corg/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.  相似文献   

3.
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.  相似文献   

4.
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.  相似文献   

5.
The variation of Cu and Zn contents with grain size was studied in the size fractions: 2000-500 μm, 500-64 μm, 64-2 μm and minus 2 μm. The fixation to different minerals was investigated in the 500-64 μm and minus 64 μm fractions with microscope, microprobe, electron microscope and X-ray diffraction after heavy-liquid separation.The distribution of Cu and Zn between the four size fractions is very similar in all target areas. The contents tend to be highest in the minus 2 μm fraction, and to decrease with increasing grain size except for an increase in the coarsest material. This feature is typical in mineralized areas with till having anomalously high Cu and Zn contents.The anomalous Cu and Zn in the till of Talvivaara are mainly fixed to chalcopyrite and sphalerite, respectively, which indicates that the main part of the material originates from fresh bedrock and that postglacial alterations are slight. In the till of Outokumpu and Maaselkä sulphides are rare. We assume that in Outokumpu the reason for this is the postglacial weathering of sulphides and that in Maaselkä a great deal of till derives from highly weathered, sulphide-poor, preglacial regolith. In both target areas Cu in till seems to fix to limonite and also to clay minerals, particularly in Maaselkä. Zinc seems mainly to be hosted by limonite in Outokumpu.  相似文献   

6.
The Lower Cambrian Saint Petersburg blue clays are composed of predominant illite and chlorite, sometimes accompanied by kaolinite. The <0.1 μm fraction has a high content of illite–smectite mixed layers. Particle-size distribution is more than 50% of clay particles and about 30% of silts. These blue clays correspond to plastic (and soft) clays; they may be compared to the Callovian clays of Bure (France), where storage of natural waste is envisaged. To cite this article: M. Arnould et al., C. R. Geoscience 334 (2002) 1135–1140.

Résumé

Les « argiles bleues » du Cambrien Inférieur de Saint-Pétersbourg sont constituées d'illite dominante et de chlorite, avec parfois présence de kaolinite. Des interstratifiés illite/montmorillonite sont très abondants dans la phase <0,1 μm. Du point de vue granulométrique, outre plus de 50% de particules argileuses, il existe une phase silteuse de l'ordre de 30%. Du point de vue pétrophysique, ce sont des argiles plastiques, de consistance molle. Elles sont subhorizontales et ont jusqu'à 116 m d'épaisseur. Outre l'absence de métamorphisme, malgré leur âge, leur caractère le plus remarquable est leur réseau de fracturation, bien observable en carrière. Les joints sont nets, sans remplissage ni cimentation. Les plans verticaux sont particulièrement développés. Le volume unitaire des blocs de matrice ne dépasse guère 1 m3. Des traces d'oxydation témoignent de circulations d'eau. Ces argiles silteuses anciennes peuvent aider à mieux connaı̂tre et comprendre les argilites silteuses épigénétiques calloviennes du site de Bure (Haute-Marne, France), où un stockage souterrain de déchets nucléaires est envisagé. Pour citer cet article : M. Arnould et al., C. R. Geoscience 334 (2002) 1135–1140.  相似文献   

7.
We have organised afield study of ocean tide loading in the northwestern part of France, where tidal amplitudes are known to be among the highest in the world. GPS and gravimetric techniques have already proved their capability to measure such weak and high-frequency signals. In this study, these classical observations are complemented with less usual techniques, such as tiltmeter and Satellite Laser Ranging (SLR) measurements. We present here the preliminary results for a common period of observations spanning from 12–19 May 2004. Additional measurements from the French Transportable Laser Ranging Station (FTLRS) were available during September and October 2004. Observation residuals are computed as the difference between the observed and the predicted time signals. We obtain small RMS residuals for GPS measurements (2.5/3.1/4.5 mm for the eastward, northward and upward components), for absolute and relative gravimetry (9 nm/s2 and 13 nm/s2) and for tiltmeters (0.05 μrad for EW component). We also fit the amplitude of the main M2 tidal constituent to FTLRS observations and we find a value of 3.731 cm, which is comparable to the theoretical value.  相似文献   

8.
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.  相似文献   

9.
Uncertainties in paleoenvironmental interpretations for traditional chemical analysis of bulk samples result from different grain-size sub-populations of sediments containing variable distributions of elements and minerals. Therefore, it is important to understand the elemental and mineral distribution in different grain sizes in determining the quantitative relationship between chemical weathering and climatic change. We sieved a series of Xiashu loess samples into three sub-populations of different grain sizes (<2, 2–45 and >45 μm, respectively), and then analyzed each population for rubidium (Rb), strontium (Sr), rare earth elements and magnetic susceptibility. In comparison with elemental concentrations of bulk samples, clay mineralogy and illitic crystallinity, our results show that distinct elemental distributions and magnetic susceptibilities for different grain-size sub-populations are controlled by sorting and/or chemical weathering, although we also suggest that the Xiashu loess may have the same provenance as the Central Chinese Loess. Maximum concentrations of Rb and fine-grained magnetic minerals in the less than 2 μm sub-population, coupled with our finding of maximum Sr in the larger than 45 μm fraction, indicate that Sr was lost during chemical weathering. Grain-size sub-population analysis is, therefore, an effective method for extracting paleoenvironmental information, because individual sub-populations show minimal variations in initial Rb/Sr ratios compared to bulk analysis of all sizes together. Furthermore, a negative correlation between Rb/Sr ratios and Sr concentrations for the <2 μm fraction (R2 = 0.97) may indicate that clay is a sensitive indicator of intensity of chemical weathering and is an ideal sub-population for determining Rb/Sr ratios, but not for magnetic susceptibility.  相似文献   

10.
A new deposit of high-quality bentonites and carbonate–palygorskite clays was discovered in the Paleogene section of the southwestern foothill of Southern Nuratau Range. The bentonites have a substantially montmorillonitic composition. Minor and admixture components are represented by illite, palygorskite, quartz, iron hydroxides, and other minerals. In terms of physicochemical properties, the bentonites are subdivided into the alkaline and alkaline-earth varieties. The carbonate–palygorskite clays possess a calcite–montmorillonite–palygorskite composition. The bentonites and carbonate–palygorskite clays formed in the alkaline medium of a marine basin. The major rock-forming montmorillonite formed as a result of the transformation of structurally similar clay minerals, while calcite and palygorskite are authigenic minerals. The bentonites and carbonate–palygorskite clays have been ascertained as a material suitable for the preparation of drilling muds, as adsorbents for the bleaching of cotton oil and purification of alcoholic products, as ointment bases and the principal component for medicinal preparations, and for other purposes.  相似文献   

11.
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.  相似文献   

12.
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.  相似文献   

13.
The amphibole metapyroxenite intrusion from Mamb (Cameroon) consists of enstatite, diopside-augite, edenite, and traces of plagioclase, biotite and rutile. It contains notable amounts of sulphides (pyrrhotite, pentlandite, chalcopyrite, pyrite and Co-rich violarite). The sulphide phase segregated during magma crystallization as immiscible droplets (≤ 1 mm) included in growing ferromagnesian minerals or aggregated in the silicate crystal mush to form an interstitial phase. However, observed sulphide assemblages are likely to result from low-T (≤ 300 °C) re-equilibration of high-T monosulphide solid solutions, more particularly during the Pan-African metamorphic event. The Mamb amphibole pyroxenite intrusion is tentatively considered as a potential source for Ni and Co mineralization.  相似文献   

14.
Far-from-equilibrium batch dissolution experiments were carried out on the 2000–500, 500–250, 250–53 and 53–2 μm size fractions of the mineral component of the B horizon of a granitic iron humus podzol after removal of organic matter and secondary precipitates. The different size fractions were mineralogically and chemically similar, the main minerals present being quartz, alkali and plagioclase feldspar, biotite and chlorite. Specific surface area increased with decreasing grain size. The measured element release rates decreased in the order 53–2>>>2000–500>500–250>250–53 μm. Surface area normalised element release rates from the 2000–500, 500–250 and 250–53 μm size fractions (0.6–77×10−14 mol/m2/s) were intermediate between literature reported surface area normalised dissolution rates for monomineralic powders of feldspar (0.1–0.01×10−14 mol/m2/s) and sheet silicates (100×10−14 mol/m2/s) dissolving under similar conditions. Element release rates from the 53–2 μm fraction (400–3000×10−14 mol/m2/s) were a factor of 4–30 larger than literature reported values for sheet silicates. The large element release rate of the 53–2 μm fraction means that, despite the small mass fraction of 53–2 μm sized particles present in the soil, dissolution of this fraction is the most important for element release into the soil. A theoretical model predicted similar (within a factor of <2) bulk element release rates for all the mineral powders if observed thicknesses of sheet silicate grains were used as input parameters. Decreasing element release rates with decreasing grain size were only predicted if the thickness of sheet silicates in the powders was held constant. A significantly larger release rate for the 53–2 μm fraction relative to the other size fractions was only predicted if either surface roughness was set several orders of magnitude higher for sheet silicates and several orders of magnitude lower for quartz and feldspars in the 53–2 μm fraction compared to the other size fractions or if the sheet silicate thickness input in the 53–2 μm fraction was set unrealistically low. It is therefore hypothesised that the reason for the unpredicted large release rate from the 52–3 μm size fraction is due to one or more of the following reasons: (1) the greater reactivity of the smaller particles due to surface free energy effects, (2) the lack of proportionality between the BET surface area used to normalise the release rates and the actual reactive surface area of the grains and, (3) the presence of traces quantities of reactive minerals which were undetected in the 53–2 μm fraction but were entirely absent in the coarser fractions.  相似文献   

15.
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.  相似文献   

16.
Lignin is preserved in the fine silt fraction of an arable Luvisol   总被引：1，自引：0，他引：1  
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.  相似文献   

17.
The results described relate to an investigation into the nature of Au dispersion in glacial till, undertaken to identify optimum search techniques for use in exploration for Au mineralization.The diversity of Au mineralization, in terms of the host rock lithologies, mineralogy and grain size of the Au, would be expected to give rise to differences in the secondary response in the associated overburden. Common exploration procedures involve the analyses of the heavy-mineral fraction or a particular size fraction of the tills. However, having regard to the expected variable response of Au in associated glacial till, attributed to variations in primary mineralization, effective exploration requires that the methodology employed is capable of locating all types of Au mineralization.Bulk till samples were collected from various sites associated with the Owl Creek deposit near Timmins and the Hemlo deposits. Grain size analyses were carried out on the till samples and on the heavy-mineral concentrates. The concentration of the Au in the various fractions was determined by Instrumental Neutron Activation Analysis.Preliminary results allow a number of provisional conclusions to be drawn:
1. (1) Grain size analysis of the −2 mm fraction of tills indicates that the silt and clay fraction constitutes 20–50%, whereas, in contrast, the equivalent heavy-mineral concentrates are dominantly composed of the coarser −500 + 63 μm material.
2. (2) The amount of Au present in the heavy-mineral concentrates of tills represents only a minor proportion of the total Au in the original till samples. In addition, the proportion of the total Au recovered in the heavy-mineral concentrate varies from 4 to 15%. Both factors indicate that caution is necessary in interpreting the significance of heavy-mineral Au data.
3. (3) Examination of the size distribution of Au within the heavy-mineral concentrate indicates that the majority of the Au is contained in the −125 μm fraction.
4. (4) The concentration factor (the original sample weight divided by the heavy-mineral concentrate weight) varies up to 7-fold between samples due presumably to the differing proportions of heavy minerals. Hence, in Au deposits of equivalent economic significance this gives rise to varying Au concentrations in heavy-mineral concentrates according to the quantity of heavy minerals present. Significant interpretation can only be achieved by re-expressing the Au contents of heavy-mineral concentrates in terms of the absolute amount of Au in heavy-mineral concentrates.
5. (5) A comparison of the heavy-mineral concentrates produced by different laboratories indicates marked differences in the weight of the heavy-mineral concentrate, the Au concentration of the heavy-mineral concentrate, the total weight of Au in the heavy-mineral concentrate and the size distribution of the Au in the heavy-mineral concentrate.
6. (6) Analysis of the −63 μm silt and clay size fraction indicates anomalous Au contents within this fraction of the tills collected from Owl Creek and Hemlo, extending over 500 m down-ice from mineralization at Hemlo.
7. (7) Analysis of the −63 μm silt and clay size fraction is suitable for the detection of fine-grained Au deposits that are not amenable to detection on the basis of heavy-mineral concentrate analyses.
8. (8) The analysis of the silt and clay fraction reduces the sample representativity problems associated with analyzing coarser fractions.
9. (9) A comparison of the Au distribution in heavy-mineral concentrates and the −63 μm fraction of till down-ice from the Owl Creek deposit indicates broadly similar dispersion patterns.
In conclusion, although the results are based on relatively few samples, their consistency permits some general conclusions to be drawn. The silt and the heavy-mineral concentrate analyses provide different information and in view of the diversity of exploration targets and surface environments exploration reliability can be increased by analyzing both the −63 μm silt and clay fraction and the heavy-mineral concentrate.  相似文献   

18.
Geochemical patterns for elements, such as Sn, W and Au, present in drainage sediments as resistate heavy minerals are often erratic and difficult to interpret. To investigate the source of these problems and develop methods of eliminating them we have compared the behavior of Sn, present as cassiterite, and associated pathfinder elements downstream from a small primary Sn deposit in Perak, Peninsular Malaysia.Dispersion trains for the pathfinder elements are characterized by smooth decay patterns and differences in concentrations between high- and low-energy environments, characterized by coarse-and medium-grained sands respectively, are not significant. In contrast, Sn (and magnetite) concentrations are extremely erratic with significantly higher concentrations in high- compared to low-energy environments. As a result the dispersion train for Sn exhibits no regular decay pattern away from its source. These findings suggest that the action of the stream is analogous to that of sluice box, with light minerals being winnowed away and cassiterite, together with magnetite, accumulating. For all but the finest sizes this process, which is most efficient in high-energy environments, causes considerable local variability in Sn content of the sediments. However, because the hydraulic behavior of cassiterite and magnetite is similar, but magnetite is not associated with the primary mineralization, the Sn/magnetite ratio can be used to eliminate Sn anomalies resulting from local variations in hydraulic conditions.The concept of hydraulic equivalence of cassiterite and magnetite was extended to examining the relationship between Sn and different size fractions of the light minerals that constitute the bulk of most sediments. Greatest contrast is obtained when the Sn content of the −270 mesh (−53 μm) fraction is re-expressed as its hydraulic equivalent concentration in −65 + 100 mesh (−212 + 150 μm) material.For exploration purposes it is concluded that: (1) providing cassiterite is present in the fine size fractions, sampling of this material will reduce hydraulic effects, thereby reducing data variability, and can also increase the length of the anomalous dispersion train; and (2) hydraulic effects can also be reduced by re-expressing Sn concentrations as ratios to magnetite (provided this is not associated with the primary Sn mineralization) or a hydraulically equivalent size fraction of the light minerals that constitute the bulk of the sediment. Similar principles probably apply to the interpretation of geochemical data for other elements dispersed in drainage sediments as heavy minerals; this warrants further investigation.  相似文献   

19.
Copper speciation in a collection of Japanese geochemical reference materials (JSO‐1, JLk‐1, JSd‐1, ‐2, ‐3 and ‐4, JMs‐1 and JMs‐2) was achieved by sequential extraction and characterised using X‐ray absorption near‐edge structure spectroscopy. In the first step of the extraction, referred to as the acid fraction, between 1% and 20% total Cu within the reference materials was extracted. Such a result is typically accounted for by absorption of Cu onto clay minerals. However, the presence of Cu sulfate (an oxidation product of chalcopyrite) was observed in some of the stream sediments affected by mining activity (JSd‐2 and JSd‐3) instead. Copper was extracted in the reducible fraction (targeting Fe hydroxide and Mn oxide) (2–49% total Cu). Between 2% and 51% Cu was extracted in the oxidised fraction (targeting sulfides and organic matter). X‐ray absorption near‐edge structure spectroscopy clarified that the reducible fraction consisted of Cu bound to Fe hydroxide, whereas the oxidised fraction was a mixture of Cu bound to humic acid (HA) and Cu sulfide. In the oxidisable fraction, chalcopyrite was the predominant species identified in JSd‐2, and Cu bound to HA was the major species identified in JSO‐1 (a soil sample).  相似文献   

20.
I Van der Molen   《Tectonophysics》1981,73(4):323-342
Measurements are presented of volume changes in granite during room-temperature compression to 100, 200 and 300 MPa confining pressure followed by temperature increase to 900°C. Comparison with thermal expansion and compressibility data for the constituent minerals allows changes in porosity to be estimated. Under confining pressure, porosity is found to decrease with heating to 200°C through expansion of the minerals into cracks which are thought to be related to the geological cooling history of the rock. Between 200°C and 840°C porosity increases as a result of differential thermal expansion of the constituent minerals, but crack opening is increasingly suppressed at higher confining pressures. Extrapolation of the results indicates that differential thermal expansion can no longer cause crack opening in dry granite at confining pressures in excess of 450 MPa. The quartz α-β transition temperature in granite is marked by a kink in the thermal expansion curve of the rock, and it is found to increase by 60°C–70°C per 100 MPa confining pressure, as opposed to the published value of 26°C per 100 MPa for single crystals of quartz. Equations are presented which allow calculation of the effects of confining pressure and temperature on the stresses and displacements in and around a spherical inclusion embedded in a matrix of different elasticity and thermal expansion. The theory, together with a simple self-consistent model for granite, accounts semiquantitatively for the observations of thermal expansion and the effect of confining pressure thereon, and for the observed α-β transition temperatures for quartz in granite.  相似文献   

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