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.     

Geochemical exploration at yandera porphyry copper prospect, Papua New Guinea

A case history is presented describing geochemical exploration of the porphyry Cu-Mo system at Yandera in the Bismark Ranges of Papua New Guinea. Three phases of geochemistry are discussed: (1) stream sediment, (2) ridge and spur, and (3) detailed rock and soil from contour trails. Results of each phase are presented and their relationship to drill-indicated mineralisation discussed. The effectiveness of the three techniques and various elements as geochemical guides to primary mineralisation is compared.Copper in stream sediment samples at a density of one sample per 1–2 km² effectively delineated the porphyry Cu system. The extent of ridge and spur sampling was limited, therefore its effectiveness is uncertain. Detailed sampling along contour trails indicated that Au and Mo are the most effective geochemical tools. Copper geochemistry is of limited use as its distribution is largely a function of recent processes and dispersion from supergene mineralisation. No clear relationship exists between Ag geochemistry and mineralisation. Lead and Zn are distributed peripheral to the porphyry Cu system.The effectiveness of Au and, to a lesser extent, Mo as geochemical guides to ore in the steep mountainous terrain of the prospect area where high rainfall, deep weathering and rapid erosion prevail is due to the relatively high stability of these metals in the soils and the oxide zone.     

Geological controls on soil parent material geochemistry along a northern Manitoba–North Dakota transect

As a pilot study for mapping the geochemistry of North American soils, samples were collected along two continental transects extending east–west from Virginia to California, and north–south from northern Manitoba to the US–Mexican border and subjected to geochemical and mineralogical analyses. For the northern Manitoba–North Dakota segment of the north–south transect, X-ray diffraction analysis and bivariate relations indicate that geochemical properties of soil parent materials may be interpreted in terms of minerals derived from Shield and clastic sedimentary bedrock, and carbonate sedimentary bedrock terranes. The elements Cu, Zn, Ni, Cr and Ti occur primarily in silicate minerals decomposed by aqua regia, likely phyllosilicates, that preferentially concentrate in clay-sized fractions; Cr and Ti also occur in minerals decomposed only by stronger acid. Physical glacial processes affecting the distribution and concentration of carbonate minerals are significant controls on the variation of trace metal background concentrations.     

Geochemical challenges of diverse regolith-covered terrains for mineral exploration in China

In recent years mineral exploration has concentrated on concealed deposits in regolith-covered terrains. In China, the regolith-covered landscapes mainly include desert windblown sand basins, desert peneplains, semi-arid grassland, loess plateaus, forestry land, alluvial plains and laterite terrains. These diverse regolith-covered areas represent geochemical challenges for mineral exploration in China. This paper provides an overview of recent progress on mechanisms of metal dispersion from the buried ore deposits through the transported cover to the surface and penetrating geochemical methods to detect the anomalies. Case studies show that, in arid and semi-arid desert sand-covered terrains, sampling of fine-fraction (− 120 mesh, < 0.125 mm) clay-rich horizon soil is cost-effective for regional geochemical surveys for sandstone-type uranium, gold, and base metal deposits. Fine-fraction sampling, selective-leaching and overburden drilling geochemical methods can effectively indicate the 210 gold ore body at Jinwozi goldfield. In alluvium-covered terrains, fine-grained soil sampling (− 200 mesh, < 0.074 mm) combined with selective leaching geochemistry shows clear ring-shaped anomalies of Cu and Ni over the Zhouan concealed Cu–Ni deposit. In laterite-covered terrains, the anomalies determined by the fine-fraction soils and selective leaching of absorbed metals on coatings of Fe–Mn oxides coincide well with the concealed deposit over the Yueyang ore deposits at the Zijin Au–Cu–Ag field. Nanoparticles of hexagonal crystals mainly native copper, gold and alloys of Cu–Fe, Cu–Fe–Mn, Cu–Ti, and Cu–Au were observed in gases, soils and ores using a transmission electron microscope (TEM). The findings imply that nanoparticles of gold and copper may migrate through the transported cover to the surface. Uranium is converted to uranyl ions [UO₂^2 +] under oxidizing conditions when migrating from ore bodies to the surface. The uranyl ions are absorbed on clay minerals, because clay layers have a net negative charge, which needs to be balanced by interlayer cations. Nanoparticles of Au and Cu and ion complexes of U are more readily absorbed onto fine fractions of soils containing clays, colloids, oxides and organic matters. Thus, fine-grained soils enriched with clays, oxides and colloids are useful media for regional geochemical surveys in regolith-covered terrains and in sedimentary basins. Fine-fraction soil sampling combined with selective leaching geochemistry is effective for finding concealed ore bodies in detailed surveys. Penetrating geochemistry at surface sampling provides cost-effective mineral exploration methods for delineation of regional and local targets in transported cover terrains.     

Continental-scale patterns in soil geochemistry and mineralogy: Results from two transects across the United States and Canada

In 2004, the US Geological Survey (USGS) and the Geological Survey of Canada (GSC) initiated a pilot study that involved collection of more than 1500 soil samples from 221 sites along two continental transects across Canada and the United States. The pilot study was designed to test and refine protocols for a soil geochemical survey of North America. The two transects crossed a wide array of soil parent materials, soil ages, climatic conditions, landforms, land covers and land uses. Sample sites were selected randomly at approximately 40-km intervals from a population defined as all soils of the continent. At each site, soils representing 0 to 5 cm depth, and the O, A, and C horizons, if present, were collected and analyzed for their near-total content of over 40 major and trace elements. Soils from 0–5 cm depth were also collected for analysis of organic compounds. Results from the transects confirm that soil samples collected at a 40-km spacing reveal coherent, continental- to subcontinental-scale geochemical and mineralogical patterns that can be correlated to aspects of underlying soil parent material, soil age and climate influence. The geochemical data also demonstrate that at the continental-scale the dominance of any of these major factors that control soil geochemistry can change across the landscape. Along both transects, soil mineralogy and geochemistry change abruptly with changes in soil parent materials. However, the chemical influence of a soil’s parent material can be obscured by changing climatic conditions. For the transects, increasing precipitation from west to east and increasing temperature from north to south affect both soil mineralogy and geochemistry because of climate effects on soil weathering and leaching, and plant productivity. Regional anomalous metal concentrations can be linked to natural variations in soil parent materials, such as high Ni and Cr in soils developed on ultramafic rocks in California or high P in soils formed on weathered Ordovician limestones in central Kentucky. On local scales, anomalous metal concentrations recognized in soil profiles, such as high P in soils from animal confinement sites, are consistent with local anthropogenic disturbances. At a larger scale, the distribution of Hg across the west to east transect demonstrates that it can be difficult to distinguish between natural or anthropogenic contributions and that many factors can contribute to an element’s spatial distribution.Only three samples in a subset of seventy-three 0–5 cm depth soil samples from the north to south transect had organochlorine pesticides values above the method detection limit, apparently related to historic usage of the pesticides DDT and dieldrin.     

A regional-scale study of chromium and nickel in soils of northern California, USA

A soil geochemical survey was conducted in a 27,000-km² study area of northern California that includes the Sierra Nevada Mountains, the Sacramento Valley, and the northern Coast Range. The results show that soil geochemistry in the Sacramento Valley is controlled primarily by the transport and weathering of parent material from the Coast Range to the west and the Sierra Nevada to the east. Chemically and mineralogically distinctive ultramafic (UM) rocks (e.g. serpentinite) outcrop extensively in the Coast Range and Sierra Nevada. These rocks and the soils derived from them have elevated concentrations of Cr and Ni. Surface soil samples derived from UM rocks of the Sierra Nevada and Coast Range contain 1700–10,000 mg/kg Cr and 1300–3900 mg/kg Ni. Valley soils west of the Sacramento River contain 80–1420 mg/kg Cr and 65–224 mg/kg Ni, reflecting significant contributions from UM sources in the Coast Range. Valley soils on the east side contain 30–370 mg/kg Cr and 16–110 mg/kg Ni. Lower Cr and Ni concentrations on the east side of the valley are the result of greater dilution by granitic sources of the Sierra Nevada.Chromium occurs naturally in the Cr(III) and Cr(VI) oxidation states. Trivalent Cr is a non-toxic micronutrient, but Cr(VI) is a highly soluble toxin and carcinogen. X-ray diffraction and scanning electron microscopy of soils with an UM parent show Cr primarily occurs within chromite and other mixed-composition spinels (Al, Mg, Fe, Cr). Chromite contains Cr(III) and is highly refractory with respect to weathering. Comparison of a 4-acid digestion (HNO₃, HCl, HF, HClO₄), which only partially dissolves chromite, and total digestion by lithium metaborate (LiBO₃) fusion, indicates a lower proportion of chromite-bound Cr in valley soils relative to UM source soils. Groundwater on the west side of the Sacramento Valley has particularly high concentrations of dissolved Cr ranging up to 50 μg L⁻¹ and averaging 16.4 μg L⁻¹. This suggests redistribution of Cr during weathering and oxidation of Cr(III)-bearing minerals. It is concluded that regional-scale transport and weathering of ultramafic-derived constituents have resulted in enrichment of Cr and Ni in the Sacramento Valley and a partial change in the residence of Cr.     

Geochemical exploration for base and precious metal sulphides associated with the Jimberlana Dyke, Western Australia

A geochemical exploration case history is described, dealing with the search for Ni and Cu sulphides, platinoids and chromite associated with the Jimberlana Dyke in Western Australia. The Jimberlana Dyke is a strongly differentiated mafic-ultramafic intrusive exhibiting similarities with the Great Dyke of Rhodesia.Soil sampling was used as the main search technique, the minus 80-mesh fraction of the near-surface soils being analysed for Ni, Cu, Co and Cr by atomic absorption spectrophotometry. Evaluation methods relied initially on visual inspection of element profile plots. Follow-up soil sampling and auger drilling were carried out in anomalous areas to define targets for deeper drill-testing. Subsequent statistical evaluation of the geochemical data has largely confirmed the initial interpretation but has in addition helped to elucidate the excellent correlation existing between the near-surface soil sampling and bedrock geochemistry.The programme was successful in locating a number of occurrences of sulphide mineralization, many of which contained copper and nickel sulphides. The most significant anomaly was at Bronzite Ridge, being related to a small pipe-like body of sulphides with grades up to 2% Ni and 2% Cu. All sulphide intersections tested recorded low values for the platinoid metals. No significant chromite segregations were located and high Cr values in soils (> 1%) can be attributed to a combination of lateritic and eluvial concentration processes.Although no economic mineralization was located the programme demonstrated the extreme sensitivity of Cu as an indicator of sulphides even through moderately thick soil cover.     

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.     

Estimation of weathering rates for critical load calculations in Finland

 The formation of base cations through mineral weathering in forest soils is one of the key parameters in calculating critical loads. Weathering rates in Finland have been estimated using a variety of methods. In the first approach, three weathering rate categories were assigned to soils according to the bedrock type. The second approach was based on an empirical relationship obtained from Swedish field studies. Changes in zirconium content through the soil profile were used to estimate element losses in soil after deglaciation. These calculated losses correlated well with the total calcium and magnesium concentrations in till C-horizons and the effective temperature sum (ETS). Comprehensive geochemical data for the parent till fine fraction (<0.06 mm) was available through the reconnaissance scale till geochemical mapping program of the Geological Survey of Finland (GSF). The equations obtained from Swedish studies were based on the use of the coarse (<2.0 mm) till fraction, and the differences in element concentrations between the fine and coarse size fractions remained a potential source of uncertainty estimating overall weathering rates. In the third approach, new geochemical data from the <2.0 mm till fraction from southern Finland were used to make new weathering rate estimates. The use of soil geochemistry instead of bedrock map classification clearly led to an improvement in the estimates of soil weathering rates in glacied terrains. The use of the fine till fraction (<0.06 mm) in the zirconium approach generally resulted in overestimations of the weathering rate. The new geochemical data for the coarse till fraction (<2 mm) are now consistent with the input requirements of the zirconium method, although the results still require further evaluation. Finnish soil profiles have a shorter weathering history than most of the Swedish ones and the uppermost layer in Finnish podsols has in some cases developed in a different till layer than the C-horizon. Received: 15 October 1995 · Accepted: 8 March 1996     

Groundwater and soil geochemistry of the Eastern Kopaida region (Beotia, central Greece)

The Kopaida plain is a cultivated region of Eastern Greece, with specific characteristics related to the paleogeographic evolution and the changes in land use of the area. This study examines the geochemical conditions of the groundwater and soil, and the correlations between them. 70 samples (50 samples of groundwater and 20 samples of soil) were collected in order to asses the geochemical status and the major natural and manmade affecting processes in the region. Extended chemical analyses were carried out including the assessment of 28 parameters for groundwater and 13 for soil samples. The results revealed that groundwater geochemistry is influenced primary by natural processes such as the geological background, and secondary by manmade impact mainly deriving from the extended use of Nitrogen-fertilizers and the over-exploitation of boreholes. Soil geochemistry is influenced exclusively by natural processes, such as weathering of the prevailing geological formations. Chemical analyses and the statistical processing of data revealed that the major factor for the geochemical status of soils is the weathering of the karstic substrate, as well as the existing lateritic horizons and a weak sulfide mineralization.     

Significance of weathering and regolith/landscape evolution for mineral exploration in the NE Albany-Fraser Orogen,Western Australia

The Albany-Fraser Orogen (AFO), southeast Western Australia, is an underexplored, deeply weathered regolith-dominated terrain that has undergone complex weathering associated with various superimposed climatic events. For effective geochemical exploration in the AFO, integrating landscape evolution with mineralogical and geochemical variations of regolith and bedrock provides fundamental understanding of mechanical and hydromorphic dispersion of ore and pathfinder elements associated with the different weathering processes.In the Neale tenement, northeast of the AFO, a residual weathering profile that is 20-55 m thick was developed under warm and humid climatic conditions over undulating Proterozoic sheared granitoids, gneisses, schists and Au-bearing mafic rocks. From the base, the typical weathering profile consists of saprock, lower ferruginous saprolite, upper kaolinitic saprolite and discontinuous silcrete duricrust or its laterally coeval lateritic residuum. These types of duricrusts change laterally into areas of poorly-cemented kaolinitic grits or loose lateritic pisoliths and nodules.Lateritic residuum probably formed on remnant plateaus and was transported mechanically under arid climatic conditions over short distances, filling valleys to the southeast. Erosion of lateritic residuum exposes the underlying saprolite and, together with dilution by aeolian sands, constitutes the transported overburden (2-25 m thick). The reworked lateritic materials cover the preserved silcrete duricrusts in valleys. The lower ferruginous saprolite and lateritic residuum are well developed over mafic and sulphide-bearing bedrocks, where weathering of ferromagnesian minerals and sulphides led to enrichment of Fe, Cu, Ni, Cr, Co, V and Zn in these units. Kaolinitic saprolite and the overlying pedogenic silcrete are best developed over alkali granites and quartzofeldspathic gneisses, which are barren in Au and transition elements, and enriched in silica, alumina, rare earth and high field strength elements.A residual Au anomaly is formed in the lower ferruginous saprolite above a Au -bearing mafic intrusion at the Hercules prospect, south of the Neale tenement, without any expression in the overlying soil (< 20 cm). Conversely, a Au anomaly is recorded in the transported cover, particularly in the uppermost 3 m at the Atlantis prospect, 5 km southwest of the Hercules prospect. No anomalies have been detected in soils using five different size fractions (> 2,000 μm, 2,000-250 μm, 250-53 μm, 53-2 μm and < 2 μm). Therefore, soil cannot be efficiently applied as a reliable sampling medium to target mineralization at the Neale tenement. This is because mechanical weathering was interrupted by seasonal periods of intensive leaching under the present-day surface conditions and/or dilution by recently deposited aeolian sediments which obscure any signature of a potential Au anomaly in soils. Therefore, surface soil sampling should extend deeper than 20 cm to avoid dilution by aeolian sands and seasonal leaching processes. Regolith mapping and the distinction between the residual and transported weathering products are extremely significant to follow the distal or proximal mineralization.     

A threshold in soil formation at Earth’s arid-hyperarid transition

The soils of the Atacama Desert in northern Chile have long been known to contain large quantities of unusual salts, yet the processes that form these soils are not yet fully understood. We examined the morphology and geochemistry of soils on post-Miocene fans and stream terraces along a south-to-north (27° to 24° S) rainfall transect that spans the arid to hyperarid transition (21 to ∼2 mm rain y⁻¹). Landform ages are ? 2 My based on cosmogenic radionuclide concentrations in surface boulders, and Ar isotopes in interbedded volcanic ash deposits near the driest site indicate a maximum age of 2.1 My. A chemical mass balance analysis that explicitly accounts for atmospheric additions was used to quantify net changes in mass and volume as a function of rainfall. In the arid (21 mm rain y⁻¹) soil, total mass loss to weathering of silicate alluvium and dust (−1030 kg m⁻²) is offset by net addition of salts (+170 kg m⁻²). The most hyperarid soil has accumulated 830 kg m⁻² of atmospheric salts (including 260 kg sulfate m⁻² and 90 kg chloride m⁻²), resulting in unusually high volumetric expansion (120%) for a soil of this age. The composition of both airborne particles and atmospheric deposition in passive traps indicates that the geochemistry of the driest soil reflects accumulated atmospheric influxes coupled with limited in-soil chemical transformation and loss. Long-term rates of atmospheric solute addition were derived from the ion inventories in the driest soil, divided by the landform age, and compared to measured contemporary rates. With decreasing rainfall, the soil salt inventories increase, and the retained salts are both more soluble and present at shallower depths. All soils generally exhibit vertical variation in their chemistry, suggesting slow and stochastic downward water movement, and greater climate variability over the past 2 My than is reflected in recent (∼100 y) rainfall averages. The geochemistry of these soils shows that the transition from arid to hyperarid rainfall levels marks a fundamental geochemical threshold: in wetter soils, the rate and character of chemical weathering results in net mass loss and associated volumetric collapse after 10⁵ to 10⁶ years, while continuous accumulation of atmospheric solutes in hyperarid soils over similar timescales results in dramatic volumetric expansion. The specific geochemistry of hyperarid soils is a function of atmospheric sources, and is expected to vary accordingly at other hyperarid sites. This work identifies key processes in hyperarid soil formation that are likely to be independent of location, and suggests that analogous processes may occur on Mars.     

Lithogenic concentrations of trace metals in soils and saprolites over crystalline basement rocks: A case study from SW Nigeria

In this study, an assessment of the lithogenic concentrations of trace metals in soils and saprolite over basement rock units in Ibadan, SW-Nigeria is presented in respect of bedrock types and geochemical controls on the weathering-associated release of trace metals. Consequently, soil, weathered and fresh rock samples from the Precambrian Basement of SW Nigeria were collected from three different bedrock units within Ibadan metropolis and subjected to mineralogical and geochemical analyses. The analytical results revealed major proportions of oxides in the range of 18–20% Al₂O₃, 2–6% Na₂O and 1–6% K₂O for weathered profiles over granite-gneiss and pegmatite units, compared to 2–3% Al₂O₃, <0.5% Na₂O and <1.0% K₂O over schist-quartzite. For the trace elements, weathered profiles on granite-gneiss and schist-quartzite settings exhibit similar enrichment trends (enrichment factor, EF l) for most of the trace elements, unlike the pegmatite bedrock. However, enrichments are relatively greater in the top soil unit compared to the intermediate saprolite unit, especially for Pb, Ni, Zn, Cr, Co, Rb, Sr and Ba, a situation attributed to leaching and redistribution within the weathered profiles through pedogenetic process and percolating groundwater.Furthermore, the estimated weathering indices using Ruxton Ratio (RR = {SiO₂/Al₂O₃}) and Chemical Index of Alteration (CIA = 100{Al₂O₃/[Al₂O₃ + CaO + Na₂O + K₂O]}) revealed RR of 2.9–3.7 and CIA of 54–73% for granite-gneiss and pegmatite units, implying medium levels of weathering, compared to RR of 30.8–35.5 and CIA of >60% for schist-quartzite units, which suggest weak chemical weathering. Also, the estimated high percentage loss, especially for Pb, Rb, Sr, Ba relative to the bedrocks, shows that the trace elements can be mobilized within the weathering profiles even at a low degree of chemical weathering. Such weathering-induced release of trace metals is of environmental significance as natural lithogenic input sources and as background reference for future monitoring of possible human/anthropogenic impacts.     

Surface geochemical and biogeochemical expression of base‐metal mineralization at Woodlawn,New South Wales,Australia

The presence of base‐metal mineralization at Woodlawn was first recognised early in 1968 when a roadside reconnaissance geochemical sampling survey, conducted over felsic volcanic rocks in the Goulburn‐Tarago area, encountered anomalous B horizon soils containing up to 200 ppm Cu, 800 ppm Pb and 300 ppm Zn. Regional soil thresholds have been determined at 50 ppm Cu, 90 ppm Pb and 50 ppm Zn. Chip samples from the subsequently located gossan revealed up to 2000 ppm Cu, 8000 ppm Pb and 2000 ppm Zn, 500 ppm Sn, 25 ppm Ag and 3000 ppm As.

The first grid B horizon soil geochemical survey was conducted in 1968 over the gossan and surrounding area, and repeated with closer spaced sampling in the first half of 1970. The first survey delineated strong Cu (to 1000 ppm) and Pb (to 2500 ppm) anomalies coincident with the gossan zone, and intense hydromorphic zinc anomalies (to 3000 ppm) located down slope from the gossan in residual clay‐soils derived from dolerite bedrock. Threshold values have been determined at 140 ppm Cu, 700 ppm Pb and 580 ppm Zn. Ag and Sn in B horizon soils show pronounced anomalies coincident with the gossan and are suitable metals for geochemical target definition. Of fourteen trace elements determined in 1974 from B and C horizon soils on two lines across the ore zone Cu, Pb, Zn, Se, Ba, Sn and Ag show direct correlation with the mineralization, whereas Cd and Mn show moderate hydromorphic dispersion, having accumulated principally in clay soils derived from dolerite weathering. As, Sb and Bi, whilst responding over the ore zone, show elevated values in soils over hanging‐wall units; Ni and Co show maximum levels in soils over dolerite bedrock.

Bark and leaves of Acacia mearnsii, collected from a line across the gossan, contain anomalous levels of Cu, Pb, Zn, Sn and Ti near the ore zone, and weaker, but clearly anomalous Mn and Ni levels over dolerite bedrock. Both bark and leaves of Acacia mearnsii reflect the presence of concealed mineralization. The shrub Solanum linearifolium grows preferentially over and close to the Woodlawn ore zone, where it contains up to 840 ppm Cu, 250 ppm Pb, 7300 ppm Zn, 6 ppm Sn and 250 ppm Ti in leaf ash compared with levels of 200 ppm Cu, 2 ppm Pb, 400 ppm Zn, 0.8 ppm Sn and 60 ppm Ti in plants growing 1.5 km from the ore zone. This shrub has potential as an indicator of base‐metal mineralization.     

Evolution of regoliths and landscapes in deeply weathered terrain — implications for geochemical exploration

Thick, commonly lateritic, regoliths are widespread in inter-tropical regions of the world and present particular challenges in exploration. These are best tackled through a sound understanding of the evolution of the landscapes in which they occur. The regoliths formed under humid, warm to tropical conditions and, although they may have been modified by later climatic changes, i.e., to more humid or more arid conditions, many chemical and mineralogical characteristics are retained. These include the geochemical expressions of concealed mineralization. Erosional and depositional processes control the preservation and occurrence of specific regolith units that may be used as sample media and, in turn, target size, element associations and contrast, thereby influencing sampling procedures, analysis and data interpretation. These parameters are best summarized in terms geochemical dispersion models based on the degree of preservation of the pre-existing lateritic regolith. Regolith–landform mapping permits an assessment of the terrain in terms of such models. In relict regolith–landform regimes, in which the lateritic regolith is largely preserved, broad multi-element anomalies in the upper ferruginous horizons (lateritic residuum) can be detected using sample intervals of 1 km or more. In contrast, in erosional regimes, where this material is absent, anomalies in upper saprolite, and the soil and lag derived from it, are more restricted in area and closer sampling intervals, (200×40 m or less) may be necessary. Lag and soil are, generally, ineffective in depositional areas, except where the sediments are very thin (e.g.,<2 m) or overburden provenance can be established. Stratigraphic drilling is necessary to establish whether the overburden overlies a buried lateritic horizon or an erosion surface cut in saprolite. Lateritic residuum remains an excellent sample medium if present, again with widespread haloes, but where it is absent, leaching and the restricted haloes in upper saprolite present formidable problems. Ferruginous saprolite or composites across the unconformity may be effective, but otherwise carefully targeted drilling and sampling through saprolite and saprock may be necessary. Partial extraction analyses have yet to demonstrate significant results except in very specific environments. In arid regions, pedogenic carbonate (calcrete, caliche) may be a valuable sample medium for Au exploration, principally in erosional regimes, and in depositional areas where the overburden is shallow. Sample intervals range from 1 km for regional surveys, through to 100×20 m in prospect evaluation. Saprolite is an essential sample medium in all landform environments, but the restricted halos and possibility of leaching requires that drilling and sampling should be at close intervals.     

The development of regolith exploration geochemistry in the tropics and sub-tropics

This essay traces the development of geochemical exploration from its early beginnings in the modern era during the 1930s, concentrating especially in its application to deeply weathered terrain in the tropics and sub-tropics. Following promising results obtained in temperate regions in North America and Europe, test orientation surveys were conducted to see whether similar procedures were applicable in the tropics, where conventional geological prospecting was largely precluded due to the extensive cover of a deep lateritic regolith and consequent lack of outcrop. After initial work in Sierra Leone and Nigeria, the emphasis transferred to East Africa in the 1950s and 1960s, aimed principally at Cu exploration. Many of the basic principles for exploration in dominantly residual, free-draining terrain were quickly established in this period. Exploration in terrains with more complex weathering histories, however, raised a number of difficulties due to leaching and secondary concentrations of elements, problems in selecting and identifying appropriate sample media, and extensive transported overburden. These were encountered especially in more arid regions in Australia and Africa during exploration for Ni and Au during the 1970s and 1980s. This led to a change in approach, placing weathering and geochemical dispersion in the context of regolith and landscape evolution –a return to the early concept of landscape geochemistry. The 3D expression of mineralization in the landscape is depicted as empirical conceptual models, that account for both relict features and active processes, and portray element associations, dispersion mechanisms and host materials. They also indicate suitable sample media, sampling intervals and procedures for analysis and interpretation.     

老万场红土型金矿成矿过程的地球化学作用

根据地质地球化学研究所揭示的与成矿地球化学作用有关的宏观和微观特征,对老万场金矿的物质来源和成矿过程的地球化学作用进行了讨论,阐述了成矿（成土）过程中Ａｕ和相关元素的地球化学行为以及本类红土型放形成的地球化学机理。指出了喀斯特红土化作用在原始卡林型金矿风化成土过程中对红土型金矿形成的影响。     

Integrated geophysical and geochemical study on AMD generation at the Haveri Au–Cu mine tailings,SW Finland

The Haveri tailings area contains 1.5 Mt of sulfide-bearing waste from the Au–Cu mine that operated during 1942–1961. Geophysical and geochemical methods were used to evaluate and characterize the generation of acid mine drainage (AMD). Correlations were examined among the electrical resistivity tomography (ERT) data, the total sulfide content and concentrations of sulfide-bound metals (Cu, Co, Fe, Mn, Ni, Pb and Zn) of tailings samples, and the resistivity and geochemistry of surface water. The resulting geophysical–geochemical model defines an area in the vadose tailings, where a low resistivity anomaly (<10 Ohm m) is correlated with the highest sulfide content, extensive sulfide oxidation and low pH (average 3.1). The physical and geochemical conditions, resulting from the oxidation of the sulfide minerals, suggest that the low resistivity anomaly is associated with acidic and metal-rich porewater (i.e., AMD). The lower resistivity values in the saturated zone of the central impoundment suggest the formation of a plume of AMD. The natural subsoil layer (silt and clay) and the bedrock surface below the tailings area were well mapped from the ERT data. The detected fracture zones of the bedrock that could work as leakage pathways for AMD were consistent with previous geological studies. The integrated methodology of the study offers a promising approach to fast and reliable monitoring of areas of potential AMD generation and its subsurface movement over large areas (ca. 9 ha). This methodology could be helpful in planning drill core sampling locations for geochemical and mineralogical analysis, groundwater sampling, and choosing and monitoring remedial programs.     

CHARACTERISTIC FEATURES OF THE LANDSCAPE'S GEOCHEMISTRY IN THE CENTRAL PART OF THE UST'YURT (PLATEAU)

An example of a confined geochemical cycle of minor elements, initiated and maintained almost entirely by vegetation, in a relatively rare landscape type of an isolated arid flat plateau blanketed by a fairly homogeneous mixture of autochthonous and of seemingly allochthonous poorly consolidated clastic materials. The plant-induced migration and redistribution of chemical elements involves the entire overburden of the bedrock. There is a definite enrichment of Ti, V, Cu, Ni, Co, Ga, and possibly of Zn, Cr, Sc, Sn in the <0.001 mm fraction of the soils and an enrichment or Zr and possibly of the rare earths and Pb in the 0.2 mm to 0.001 mm fraction, while the metals content of the >0.2 mm fraction is poorer in such constituents than the bedrock itself.--V. P. Sokoloff.     

Petrologic and geochemical characteristics of “barkinite” from the Dahe mine, Guizhou Province, China

Although “barkinite” has long been studied by many geologists, its geochemical characteristics and environment of deposition are still not known in detail. In order to study the petrography and geochemical characteristics of “barkinite”, coal samples from two Permian coal seams were taken from the Dahe mine, Guizhou Province. The samples were separated into maceral fractions, and then analyzed by microscopical, isotopic, Rock-Eval, and geochemical methods. The microscopical results indicate that “barkinite” occurs as four main types. According to their relationship to other maceral groups, “barkinite” is ostensibly formed under variably dry–wet or oxidizing–reducing conditions. The extract yield, isotope data and Rock-Eval values of “barkinite” are different from other macerals. Microscopical and geochemical results indicate that “barkinite” forms part of the liptinite group.