Quaternary stratigraphy and geochemistry at the Owl Creek Gold Mine, Timmins, Ontario, Canada

The Owl Creek Gold Mine is located in Hoyle Township, approximately 18 km northeast of Timmins, Ontario, Canada. The open-pit mine exposes a sequence of altered and mineralized mafic tholeiitic volcanics bounded to the north and south by greywacke and argillite. Gold occurs in the free state in quartz veins, often with graphite, and as fine gold on surfaces of, and within fractures in, pyrite.The study was designed to determine the distribution and distance of transport of Au in overburden down-ice from subcropping Au mineralization. This required an understanding of the glacial history of the area.The Quaternary stratigraphy at Owl Creek was studied and sampled by means of 17 sonic and 15 reverse-circulation overburden drill holes near the open pit, and several overburden exposures in the open-pit walls. Nonmagnetic heavy-mineral concentrates (specific gravity >3.3) were made from the <2000 μm (−10 mesh) fraction of all overburden samples from the drill hole and section sampling. The heavy-mineral concentrates were analyzed for Au by neutron activation. A till pebble lithology study was done on the >2000 μm (−10 mesh) fraction of the sonic drill core.Our stratigraphic studies indicate that there were three major Wisconsinan (Weichselian) ice advances and one minor, late readvance in the Timmins area. The transport and deposition of sediments comprising the “Oldest”, “Older”, Matheson and Cochrane stratigraphic “packages” (oldest to youngest) are related to three ice advances and one readvance which moved towards 240° ± 10°, 150° ± 5°, 170° ± 5° and 130° ± 5°, respectively.Geochemically anomalous levels of Au in the overburden define two dispersal trains down-ice of the Owl Creek Gold Mine. One, in the “Older” lodgement till, is 400–500 m long. The other in Matheson ablation and waterlain tills, is approximately 700 m long.The till pebble lithology study showed that pebble counting can be used to approximate bedrock contacts, but may not necessarily identify the source rock type of the matrix.     

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.     

The behaviour of platinum group elements in the surficial environment at Ferguson Lake, N.W.T., Rottenstone Lake, Sask. and Sudbury, Ont., Canada

A multidisciplinary geochemical study of the distribution, dispersion, and glacial dispersal, of the pge and associated elements has been undertaken within soil, till, humus, vegetation and water at Ferguson Lake, Northwest Territories, Rottenstone Lake, Saskatchewan and Sudbury, Ontario.As the pge generally are present at low levels in surficial materials, development work on analytical techniques was an essential part of this study.At Ferguson Lake, the spatial distribution patterns of Au, Pt and Pd in till clearly indicate the exposed gossan zones, as expected, but also indicate a possible extension of the zone beneath a peat bog- and till-covered area. Down-ice dispersal of Au, Pt and Pd is limited to one to two hundred metres, in the <63 μm component of the till samples collected from frost boils. In vegetation the pge enrichment extends for several hundred metres down-ice and is best defined by Pd in birch twigs. Detectable, although extremely low, levels of Pt (2.8 ppt) and Pd (2.0 ppt) are present in waters in the vicinity of the gossanous zones at Ferguson Lake.At Rottenstone Lake, moderate to high concentrations of pge, Au, and base metals were found in ashed twigs of black spruce and the hmc of the tills for a distance of less than two hundred metres down-ice of the mineralization. Low Pd and Au concentrations were present in ashed spruce twigs about one kilometre down-ice of the mineralization, where only the hmc of the tills yielded anomalous concentrations of Pt and Au. There appears to be only limited dispersal of the pge and Au. These data indicate that only the hmc and the spruce twigs are of value in detecting Pt and Au in this area. Palladium presents a different picture, being detectable in only some of the soils, absent in the tills and hmc, yet appreciably enriched in the twig ash. The inference is that Pd is moving in solution and is being somewhat adsorbed in the soil but is much more significantly being taken up by the plant roots.At the Sudbury areas the pge, hosted in the Ni-Cu mineralization, are best reflected by elevated levels in the ashed humus of almost all elements examined. There is only minimal response in pge and Au to the mineralization from any of the fractions of the soil; whereas the <2 μm fraction of the B-horizon soil reflects the mineralization by elevated levels of As, Sb, Se, Cr, Co, Ni, Cu, Pb and Zn. Only hmc from the tills show elevated pge, Au and variable enhancement in As, Sb, Se and the base metals. The < 2 μm portion of the tills tends to be highest in As, Se, Cr and the base metals.This ongoing study shows that surficial materials and vegetation are effective in identifying areas of concealed pge mineralization. Various pathfinder elements, primarily Cu and Ni, but perhaps also As, Se, Sb and the other base metals, in the < 2 μm B-horizon soils and tills, may be informative in a preliminary evaluation of the pge potential of an area, prior to undertaking the more expensive precious-metal analyses. Humus and vegetation both appear extremely effective, and most cost efficient, and heavy-mineral concentrates (hmc) appear effective, for identifying areas with pge potential, whereas hmc from tills appear most effective for zeroing in on the site of the pge mineralization.     

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.     

Pyrite of distinctive isotopic composition from the Hemlo deposit: A potential tool to identify this type of gold mineralization in Archean terrain

Most sulphides from various rock types and mineralization of Archean age exhibit sulphur isotope values (δ³⁴S) near 0‰. This is due to a general absence of conditions suitable for the oxidation-reduction reactions essential for isotopic fractionation. However, some important occurrences of Archean Au mineralization do display significant variations in δ³⁴S). One such occurrence with unusual isotopic compositions is the Hemlo gold deposit: pyrite from the ore typically has δ³⁴S < −6‰ to a minimum value of −17.5‰ The isotopic composition of the pyrite is correlated with the content of Au, indicating that they are genetically related.The sulphur isotope data suggest that sulphur compounds experienced redox reactions in the hydrothermal system at Hemlo and that sulphate was present prior to the Au mineralization. This sulphate may be of exogenic origin from a restricted basin, or of endogenic origin from magmatic-hydrothermal fluids. Other characteristic features of the deposit, such as enrichment in Sb, Tl and Hg, may also be explained by ore deposition under moderately oxidizing conditions.Distinctive δ³⁴S values were also observed in pyrite from Au mineralization at Heron Bay, 30 km west of Hemlo, and from baritic strata 21 to 27 km west and on approximate strike from Hemlo. These occurrences also represent sulphate-bearing hydrothermal systems and, as such, give distant information on the unusual environment of the mineralization at Hemlo. Since the isotopes of sulphur are sensitive to oxidation conditions they may be used to identify hydrothermal activities characteristic of this type of Au mineralization and to explore for other unusual areas of sulphate accumulation in Archean terrains.     

Geochemical dispersion of gold related to copper-gold mineralization in northeastern Thailand

The nature of gold dispersion in soils and stream sediments associated with a copper-gold-mineralized system in northeastern Thailand has been investigated as a basis for identifying appropriate geochemical exploration techniques for the search for comparable deposits in similar environments.Soils were collected with varying relationships to mineralization as a basis for determining sample representativity, size distribution of gold, variation with soil horizon and possible pathfinder elements. Similarly, stream sediments were collected to estimate sample representativity, size distribution of gold, variation of gold with depth in the stream sediment profile and to compare the relative recoveries of gold in field-panned and laboratory-prepared heavy-mineral concentrates. Samples were analyzed for Au and potential indicator elements by a variety of methods but mostly by instrumental neutron activation analysis.Results indicate the consistent distribution of fine-grained gold in soils which allows Au analysis of relatively small samples from B-horizon soils to be used effectively and reliably to identify the surficial patterns of gold mineralization in the study area. Anomalous patterns of other indicator elements, Co, As, Cu, Sb, W, Pb, Zn, Ag, Fe and Mn, may contribute additional information regarding type of mineralization. This finding indicates the effectiveness of soil surveys in gold exploration, particularly in areas of deep weathering where fresh bedrock exposures are infrequent.Unlike soils, size distributions of gold in stream sediments, as a result of the local flow regime, vary both between sampling sites and at depths within a sampling site. Exploration requires Au analysis of the fine fraction (minus 63 μm) of active stream sediments to reduce the problem of sampling representativity. The presence of coarse-grained gold in the stream channel has drawn attention to the possible benefit of using the conventional field-panning method as a semiquantitative technique for providing immediate results. However, highly erratic distribution of pannable gold on a very local scale together with variable proportions of the total gold recovered in field-panned or heavy-mineral concentrates highlights a potentially serious drawback of the method. Combination of analysis of the minus 63 μm fraction and field panning appears warranted to cover the possible existence of gold of a wide size range in stream sediments.The overall results indicate the utility of geochemical exploration techniques in the search for gold mineralization. However, particular care is necessary in the design and implementation of geochemical techniques to ensure maximum reliability of exploration.     

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.     

Effects of valley and local channel morphology on the distribution of gold in stream sediments from Harris Creek, British Columbia, Canada

Large (60 kg, minus 2 mm) sediment samples collected from a 5-km reach of a mature highland stream were used to investigate the effects of bar morphology and channel slope on the downstream dispersion of Au. Results are compared with those for an abundant heavy mineral (magnetite) and are discussed in terms of differential entrapment of light and heavy minerals by gravels and differences in supply of magnetite and Au to the study reach. Gold is selectively trapped in gravels; therefore, highest Au concentrations, a long dispersion train and lowest between-sampling-location variability were obtained with heavy-mineral concentrates of the minus 105+74 μm fraction from sandy gravels. In contrast, sands in bar-tail eddy pools gave the least reliable Au concentrations, due to random (Poisson) sampling errors and local post-depositional winnowing, and show rapid downstream anomaly decay.     

Geochemical studies in the Indian Pass and Picacho Peak Bureau of Land Management Wilderness study areas, imperial county, Southern California

The U.S. Geological Survey has conducted geochemical studies in the Indian Pass (CDCA-355), 124 km², and Picacho Peak (CDCA-355A), 23 km², Wilderness Study Areas (WSA's) as part of a program to evaluate the mineral resource potential of designated areas in the California Desert Conservation Area. These two WSA's are of particular interest because they lie within a region which has intermittently produced significant quantities of Au since the mid-1800's, and is currently the site of much exploration activity for additional Au resources. Within a 15-km radius of the WSA's, there is one actively producing gold mine, a major deposit which began production in 1986, and one recently announced discovery. In the reconnaissance geochemical surveys of the two WSA's - 177 μm (-80 mesh) stream sediments, heavy-mineral concentrates from stream sediments, and rocks were prepared and analyzed.Four areas of possible exploration interest were identified within the WSA's. The first area is characterized by anomalous W and Bi in nonmagnetic heavy-mineral concentrates, and is underlain primarily by the Mesozoic Orocopia Schist which has been intruded by monzogranite of Oligocene age. Alteration and mineralization appear to be localized near the intrusive contact. The mineralized rock at the surface contains secondary Cu and Fe minerals where the monzogranite intrudes the metabasite horizons of the Orocopia Schist and scheelite where the monzogranite intrudes marble within the Orocopia Schist.The second area is characterized by anomalous As, Sb, Ba, B, and Sr in nonmagnetic heavy-mineral concentrates and by anomalous As in - 177 μm stream sediments. Geologically, this area is underlain by metasedimentary and metavolcanic rocks of Jurassic(?) age; a biotite monzogranite of Jurassic(?) age; and Tertiary volcanic and hypabyssal rocks composed of flows, domes, and tuffs of intermediate to silicic composition. All these rock types are cut by a set of north-south-striking normal faults. The anomalies in the heavy-mineral concentrates are believed to be related to silica-clay alteration observed in the vicinity of some of these faults.     

Heavy-mineral concentrates from rocks in exploration for massive sulphide deposits

A number of programs have investigated the use of rock geochemistry in the search for volcanogenic massive sulphide deposits in the Canadian Shield. Regional-scale studies have been successful in differentiating productive from nonproductive volcanic cycles. Wall-rock studies have successfully delineated alteration halos related to the mineralizing event. While an alteration halo has been identified around the South Bay massive sulphide deposit, this halo does not extend far enough from the deposit to be useful for reconnaissance purposes. The authors therefore tested the possibility of enhancing detection of a primary trace-element halo by using the heavy mineral fraction of the rocks.The geochemical dispersion of trace elements in the heavy-mineral fraction of rocks was investigated around the South Bay massive sulphide deposit, in the Superior Province of the Canadian Shield. Approximately 270 samples were ground to 74–500 μm (−35 +200 mesh) and separated using the heavy liquid bromoform. Following removal of the magnetic fraction, the samples were further pulverized, and analyzed by atomic absorption spectrophotometry for Cu, Pb, Zn, Ag, Fe, Mn, Co and Ni. Corresponding whole-rock samples were analyzed to provide for a comparative study with the whole-rock geochemistry.Analysis of the heavy-mineral fraction of rocks revealed strong and extensive halos of Cu, Pb, Zn and Ag persisting in some cases up to 10 km along strike away from the South Bay Deposit. By comparison, in the whole-rock data, halos of Pb, Ag and Zn were detected no farther than 1–2 km away from the deposit. Furthermore, trace-element content in the whole rocks appeared to be dominated by rock type; either multivariate statistical techniques, or separation of the data by rock type, was necessary to distinguish the anomaly related to mineralization. Trace-element content in the heavy-mineral concentrates was dominated by the presence of the sulphide minerals pyrite, chalcopyrite, and sphalerite, thus directly reflecting mineralization.Use of the heavy-mineral fraction of the rock eliminates the dilution effects of quartz and feldspar, allowing enhancement of trace-metal concentrations in sulphide minerals, and the delineation of strong and extensive halos of Cu, Pb, Zn, Ag and Mn around the South Bay massive sulphide deposit. While the cost of preparation of heavy-mineral separates is higher than that for whole-rock samples, the anomaly clearly defined by the trace-element content of the heavy fraction avoids the need for costly major-element and subsequent statistical analysis, and increases target size by an order of magnitude. The heavy-mineral fraction obtained from rocks shows great potential as an exploration guide to volcanogenic massive sulphide deposits.     

Mobilization of gold into lake sediments from acid and alkaline mineralized environments in the southern Canadian Shield: Gold in lake sediments and natural waters

To be an effective indicator of mineralization in lake sediment surveys within the Canadian Shield, it is desirable that an element migrate in solution or adsorbed on suspensates. Given the low relief and disorganized drainage patterns of this region, dispersal in clastic form in drainage systems is limited and gives rise to erratic distributions. The purpose of this study was to discover whether Au shows significant hydromorphic mobility, which would justify the increasing use that is being made of this element in lake sediments as an indicator for gold mineralization.Waters and lake sediments were collected from Napier Lake, Ontario; PAP Lake, Saskatchewan; and Foster Lake, Manitoba, all of which contain Au-quartz vein mineralization and lie within the glaciated boreal forest zone of the Canadian Shield. In all three areas, profundal lake sediments down-drainage of mineralization contain Au concentrations higher than regional mean concentrations. Significant dissolution and transport of Au was found under oxidizing conditions associated with waters with pH that varied from acid to alkaline. Waters from drill holes penetrating mineralization contain up to 401 ng L⁻¹ Au (note; 1 ng L⁻¹ is equivalent to 1 part per trillion, 10⁻¹²). Surface waters overlying or near mineralization collected from bogs, seeps, ponds and streams contain up to 13 ng L⁻¹. The content of Au in lake waters is lower, with a maximum of 1.1 ng L⁻¹. There is also a detectable quantity of Au present in suspensates. Two samples of particulates (> 1 μm) filtered from lake water have Au equivalent to 0.17 ng L⁻¹ and 0.039 ng L⁻¹. While the contents of Au present in solution or as suspensates in lake and stream water are relatively small, they are sufficient, if precipitated, to generate anomalies in lake sediments. Thus for Reservoir Lake, in the Foster Lake area, water from the principal stream entering the lake carries 0.3 ng L⁻¹ Au. This provides an annual flux which far exceeds that required to generate the 7.3 ppb Au contained in profundal sediments of this lake; a content that is anomalous relative to the regional median content of < 1 ppb Au for lake sediments.Hydrogeochemical prospecting involving analysis for Au is one method for tracing the source of anomalous Au in lake sediments. Collection of 1 L samples without field treatment, followed by extraction of Au into MIBK, then analysis by graphite-furnace atomic absorption spectrophotometry, permits detection levels for Au of 0.5 ng L⁻¹. This is below the contents of Au found in some waters from mineralized areas. A detection limit of 0.3 ng L⁻¹ was obtained using larger water samples.     

Platinum and palladium stream-sediment geochemistry downstream from PGE-bearing ultramafics, West Andriamena area, Madagascar

Several pilot studies were made in a PGE-mineralized area of central Madagascar in order to compare Pt,Pd halos in heavy mineral concentrates and to select the most suitable stream-sediment fractions, sampling densities and anomaly thresholds for regional PGE surveys. Results show low anomaly thresholds for Pt (30 ppb) and Pd (20 ppb) in the −63 μm fractions of the active sediment, with restricted halos of nearly 300 m for Pt and nearly 500 m for Pd. Using a slightly coarser fraction (−125 μm) increases the anomaly contrast. The Pt anomalies in heavy mineral pan concentrates are considerably enhanced (400–1,000 ppb) but occur further downstream in residual terraces. A regular increase in the weight of the heavy mineral concentrate for a given volume of sediment is noticed downstream. A simple weight correction of the raw Pt grade in the heavy mineral concentrate gives a better definition of the mineralized source upstream. Assessment of the corrected heavy mineral concentrate Pt anomalies together with Pt,Pd anomalies in the finest stream-sediment fraction produces the optimum definition of the target. Optical determination and scanning electron microscope studies of the PGM show sperrylite to be the major Pt-bearing mineral in the stream sediment, whereas the Pd mineralogy remains unresolved. Pt dispersion appears to be a predominantly mechanical process and Pd dispersion a chemical process with deposition controlled mainly by MnO scavenging.     

Lithology and trace-metal content in till in the kuhmo granite-greenstone terrain, eastern Finland

Rocks of the Archaean Kuhmo greenstone belt and the fine fraction (− 63 μm) of 236 till samples were analysed for Co, Cr, Cu, Mn, Ni, Pb, Zn and Fe mainly with the AAS method. The influence of bedrock upon the lithology and geochemistry of till is clear, and can be seen immediately at the proximal contact. Expected trace-metal contents for the fine fraction of till were calculated using the average metal contents of the rock types and the proportions of these rock types in the till (2–6 cm pebbles). The expected values were then compared with the measured values in the fine fraction of till at the same locality. This approach seems effective for lithological comparison between various grain-size fractions of till.In general, the measured metal contents are clearly lower than expected. This indicates that the proportion of the greenstone material in the fine fraction of the till is smaller than in the coarse fraction. Correlations between measured and expected values of individual trace metals as well as their correlation with the different rock types are low, in most cases indicating inconsistent variation in the lithology of the coarse and fine fraction of the till. Good positive correlations between the number of pebbles of mafic metavolcanics and contents of Cu, Co, Mn and Fe in the fine fraction of till show that the influence of these rocks on the trace-element geochemistry of the tills in the study area is most significant as might be expected.     

Västanå-Järkvissle Sn-Li occurrence found by regional grid sampling of heavy-mineral till concentrates in northern central Sweden

Regional exploration for pegmatite hosted Sn-mineralization in Sweden by LKAB Prospektering has, since the early 1980s, generally been based on the use of heavy-mineral concentrates from till collected by roadside sampling. The average sampling density has been 0.5–1.0 sample/km², but with an uneven distribution of sample points within areas investigated.Planning of the regional sampling grid in this study has been based on a statistical analysis to answer the following question: What sample density and grid-spacing should be used to hit an anomalous target with the highest possible probability.The statistical analysis indicates that using a rectangular grid, 750 × 1,500 m (0.88 sample/km²), the probability of intersecting an anomalous target is 100%. Heavy-mineral till concentrate sampling using this grid design in northern central Sweden in 1981 revealed one single, extremely high sample with 4,622 ppm Sn indicating mineralization in the area north of the village of Järkvissle.In 1982–1983, while boulder tracing up-ice from the anomalous regional sample point, cassiterite and spodumene-bearing boulders and outcrops were found. Two parallel mineralized pegmatites within an area of approximately 5,000 m² with grades of 0.04–0.07% Sn and 0.40–0.92% Li₂O have recently been located NW of Järkvissle.Semi-regional (250 × 500 m) and local (20 × 20–160 m) sampling of till gave some anomalous values of Sn and Li in concentrates, which to some extent could be correlated with mineralized boulders and outcrops, and also indicated new targets for drilling.The results from a simplified sample preparation technique for heavy-mineratl till concentrates show that a new device, named the Goldhound, can be used in future geochemical prospecting for Sn and Li in Sweden.     

Mode of occurrence of Cu and Zn in till over three mineralized areas in Finland

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.     

Overburden geochemistry related to W-Cu-Mo mineralization at Sisson Brook, New Brunswick, Canada: An example of short- and long-distance glacial dispersal

In 1982 and 1983 a surficial geology and overburden geochemistry survey was carried out on the Sisson Brook Mining Licence in York County, about 55 km northwest of Fredericton, New Brunswick, Canada.On the Sisson Brook Mining Licence three zones of W-Mo-Cu mineralization have been outlined; Zones I and II contain mainly wolframite with chalcopyrite and pyrrhotite, whereas Zone III has mainly scheelite and molybdenite.The glacial history of the area was studied during 1982 and 1983 to provide a framework for interpreting the geochemical results. Ice movement varied from 160° ± 10° towards the south during the Main Bantalor phase (maximum ≈ 13,500 y.B.P.) to 130° ± 10° toward the southeast during the Late Bantalor phase. Rapid changes in dominant pebble lithologies occur immediately upon crossing bedrock contacts. This suggests a very short distance of transport on the property. The glacier, butted against the Nashwaak Ridge, quickly sheared bedrock debris up into the body of the ice by compressive flow. Upon melting, some of this debris was deposited a short distance from source. Some debris appears to have been sheared up higher into the ice sheet, transported over the Nashwaak Ridge, and deposited approximately 8 km down-ice with no interconnecting dispersal train.In 1982, a geochemical orientation survey was carried out to determine which element(s) and sample medium could best and most economically be used in the search for W-Mo-Cu mineralization. Within the property area, both whole till <2000 μm (−10 mesh) samples and heavy mineral concentrates clearly defined the zones of mineralization (W, Mo, Cu) and associated geochemical dispersal trains (W, Mo, Cu, As, F). In later work, samples were not analyzed for As and F because this provided no additional information. The geochemical contrast between values in whole till samples derived from subcropping mineralization and those derived from barren bedrock is adequate to outline mineralization. Geochemical analysis of the whole till was used in later work because the sample preparation costs are considerably lower than those for heavy-mineral concentrates. Soils were not used because trace element patterns were diffuse, with the highest values occurring at variable distances down-ice from mineralization.In 1983, the objective was to better define glacial dispersal from the known mineralization and to explore for additional mineralization. Data from this program indicates a W dispersal train in whole till samples 300–400 m long. Tungsten values up to 1400 ppm and Mo values up to 260 ppm in whole till occur immediately down-ice from the main subcropping W-Mo mineralization. The element associations (i.e. W-Mo-Cu and W-Mo) in the till reflect the elemental composition of the source mineralization (i.e. Zones I and II and Zone III).Backhoe trenching is a useful and cost-effective technique to expose Quaternary sediments. Examination of the overburden sections provides an understanding of the glacial history which aids in tracing geochemical dispersal trains up-ice to bedrock source.     

The use of “loam” concentrates in geochemical exploration in deeply weathered arid terrains

This paper reviews some aspects of the use of “loam” (soil) concentrates in geochemical surveys in arid, deeply weathered environments.An orientation survey at a small Ni-Cu-Co prospect in Western Australia has shown that discrimination between mineralized and unmineralized samples could be achieved using Ni, Cu, Co, Cr, Zn, As, Sn, Sc, Ti, Yb and Y in the coarse fraction of heavy concentrates. However, at the same prospect the best contrast for Ni, Cu and Co in surface samples was provided by analysis of the same fraction following a cold ammonium citrate/hydroxylamine hydrochloride digestion.At a nearby, larger prospect, some 54 km² in area, concentrates were separated, by jigging, from bulk soil samples, themselves composites of representative subsamples. Sampling at a density of 4 samples per km² revealed 1–2 km² size anomalies of Cu, Ni, Co, Cr, As and Au which could be related, variously, to known Ni-Cu and Au mineralization.In Botswana, analysis of concentrates, separated by tabling from samples collected at a density of 1 sample per 7.5 km² over an area of 5400 km², identified distinctive geochemical districts. Enhanced values of Au and of Cu-Ni in the concentrates were relatable to known mineralization and the results suggested that there were also Sn-W-Mo-Bi (granitoid) and Au-Pb-Zn-Bi-Sn (volcanogenic) associations which could lead to new prospecting targets. Anomalies of certain elements (for example, Cu in an ultramafic environment) may be more readily detected in surface material by “enrichment indexing” the concentrate data.     

Use of a sensitive analytical method and the silt-clay (< 53 μm) fraction of stream sediments in exploration for gold in northern Thailand

Heavy mineral concentrates (SG 3.3) from the Huai Hin Laep, a tributary of the Huai Kho Lo River in northern Thailand, contain strongly anomalous concentrations of gold. In contrast, the gold content of the associated < 149 μm and <53 μm fractions of the sediment is generally less than the 5 ppb detection limit obtained by a conventional fire assay-atomic absorption spectrometry method. To test for the presence of a gold anomaly at concentrations < 5 ppb, we have used an aqua-regia digestion followed by an Amberlite XAD-8 column preconcentration technique that, when used with a spectrometer that enables full display of the analytical spectrum to optimize baseline analysis, gives a detection limit of 0.1 ppb Au.Gold content of the < 53 μm sediment fraction ranges from 1.0 to 3.1 ppb compared to concentrations that typically range from 1000 to more than 100,000 ppb in the heavy mineral concentrates. However, despite gold concentrations in the sediment being several orders of magnitude lower than those in the heavy mineral concentrates, the downstream dispersion patterns are similar, with gold concentrations increasing at high energy sites and downstream away from the assumed source. These results identify the presence of a greatly diluted gold anomaly in the < 53 μm fraction of the sediments and suggest that transport and deposition of this fine grained gold is controlled by the same sedimentological factors that control the behavior of gold in the sand-size range, between 53 μm and 425 μm. Most important from an exploration standpoint, is that by using a sufficiently sensitive analytical method, meaningful gold dispersion patterns can be recognized at concentrations below 5 ppb.     

Mineralogical and geochemical analysis of shallow overburden as an aid to gold exploration in southwestern Gaspésie, Quebec, Canada

Mineralogical and geochemical data from shallow overburden surveys are examined to ascertain parameters which govern the distribution of gold in overburden in a 2400-km² area of southwestern Gaspésie, Quebec, Canada.The area is a deeply dissected plateau underlain by faulted and gently folded Siluro-Devonian strata. Complex geomorphic and glacial histories are reflected in the non-glacial character of the landscape, the preservation of very old erosional landforms and extensive variation in the composition and distribution of overburden.Total sample analysis and heavy-mineral studies show that the composition of overburden changes across the area in approximate correspondence with changes in underlying bedrock. Three broad zones related to bedrock and overburden types are delimited. Gold analyses of <250 μm overburden are insensitive to regional variations, with only 15 samples out of 300 registering above the detection limit of 2 ppb. Better contrasts of gold concentrations are obtained from chemical analyses of nonmagnetic heavy-mineral concentrates (NM HMC). Although sample density is low, NM HMC data show anomalies which can be related to particular bedrock and structural settings. Particulate gold was not observed in any of the NM HMC. Gold is associated with secondary iron-oxide phases replacing primary sulphide minerals. High concentrations of gold in NM HMC of overburden collected north of the mouth of the Assemetquagan River support the hypothesis of a local source to the north or northwest for the alluvial gold in the lower 2 km segment of the river.Dilution by far-travelled, shield-derived heavy minerals is by far the most important cause of regional mineral variation. Conversion of gold concentrations in NM HMC to concentrations in total size fraction eliminates some of the erratic behavior of NM HMC data caused by variations in heavy-mineral abundance and corrects for the dilution effect where the proportion of heavy minerals in the far-travelled component of overburden is much greater than in the local component. These calculations suggest a contribution of gold to the background in the fine sand fraction of overburden of 0.07 ppb. Where the diluting component is local, conversion of NM HMC data to total size fraction may or may not correct for differences in heavy-mineral contributions of underlying bedrock, depending on local conditions. Where dilution by far-travelled components is excessive, NM HMC analyses are inadequate to reflect conditions in underlying bedrock.     

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.