Application of geochemical methods in the search for geothermal fields

From 1983 to 1985, an orientation study was carried out in about 20 geothermal fields in China. Semi-detailed and detailed surveys were conducted in an area of 90 km² in Yangbajing, Tibet. Hg, As, Sb and Bi were used as indicators to extend the promising area of known geothermal fields to 16 km². In the northern part of the extended promising area, three drill holes were sunk and high-temperature thermal water of 160°C was obtained. In the southern part, outside the geochemical anomaly, two holes were drilled but no thermal water was found. The inner zone of the Hg anomaly coincides closely with the distribution of drill holes that met thermal water with temperatures higher than 140°C. The distribution of Bi values may indicate that the thermal water in the southern part is at shallower depth. A semi-regional survey in an area of 200 km² in Tengchong, Yunnan Province delineated several new prospects, which will possibly extend the resources of the Rehai geothermal field. An element zoning pattern similar to that of hydrothermal mineral deposits was discovered in the Rehai geothermal field. A semi-regional survey conducted in Xiaotangshan near Beijing indicated that the possible extent of the Xiaotangshan geothermal field may reach 30 km². Drilling confirmed that the outer zone of the Hg anomaly is in accordance with the distribution of 40°C thermal water, and the intermediate and inner zones of the Hg anomaly are associated with higher temperature thermal water. Research during the three years 1983–1985 demonstrated that exploration geochemistry is an effective tool for finding geothermal fields.     

The use of geochemical indicator elements in the exploration for hot water sources within geothermal fields

Soils, rocks, altered rocks, hot and cold waters, and hot spring precipitates were sampled within and on the outskirts of geothermal fields in China. The contents of thirty trace elements in soils and rocks show that Hg, As, Sb, Bi, Li, Rb, Cs, Au, Ag, B, W, Sn, Pb, Zn, Mn, Ni and Co can serve as direct and indirect indicators for geothermal field exploration. Large amounts of data indicate that Hg, As and Sb are the best indicators of hot water sources. Altered rocks contain higher Hg, As, Sb, Bi and Be than unaltered rocks. Based on their abundances in hot waters, it is suggested that the following elements may be used as hydrochemical indicators of high-temperature hot-water geothermal systems: K⁺, Na⁺, Ca²⁺, Mg²⁺, SO²⁻₄, HCO⁻₃, F⁻, Cl⁻, SiO₂, HBO₂, CO₂, pH, total dissolved solids and hydrochemical types, as well as Hg, As, Sb, Be, Li, Rb and Cs. Modern precipitates associated with hot springs have high contents of Ba, Be, Fe, Ti, Hg, As, Sb and Bi. Using these geochemical data, the authors have had much success in locating hot water drill sites within geothermal fields. Case histories are described for five geothermal areas.     

Distribution of some elements in surface soil over the Kavadarci region,Republic of Macedonia

The results of a first systematic study of spatial distribution of different elements in surface soil over of the Kavadarci region, Republic of Macedonia, known for its nickel industrial activity are reported. The investigated region (360 km²) is covered by a sampling grid of 2 × 2 km²; whereas the sampling grid of 1 × 1 km² was applied in the urban zone and around the ferronickel smelter plant (117 km²). In total 344 soil samples from 172 locations were collected. At each sampling point soil samples were collected at two depths, topsoil (0–5 cm) and bottom soil (20–30 cm). Inductively coupled plasma-mass spectrometry (ICP-MS) was applied for the determination of 36 elements (Ag, Al, As, Au, B, Ba, Bi, Ca, Cd, Co, Cr, Cu, Fe, Ga, Hg, K, La, Mn, Na, Mg, Mo, Ni, P, Pb, S, Sb, Sc, Se, Sr, Th, Tl, Ti, U, V, W and Zn). Data analysis and construction of maps were performed using the Paradox (ver. 9), Statistica (ver. 6.1), AutoDesk Map (ver. 2008) and Surfer (ver. 8.09) software. Four geogenic and three anthropogenic geochemical associations were established. Within the research, natural and anthropogenic enrichment with heavy metals was determined. Principally, the natural enrichment is related especially to Ni. Pollution by As, Cd, Co, Cr, Cu, Hg, Mo, Pb and Zn is basically insignificant.     

西藏羊八井热田的碱金属元素研究

本文研究了西藏羊八井高温地热田及毗邻90km²范围内土壤中碱金属元素的地球化学特征,结果表明,碱金属元素锂、铷和铯可以作为一组新的地球化学指标用于热田勘查,圈定热田范围,其作用与已提出的汞、砷、锑和铋地球化学指标相类似。文章对碱金属元素在地热系统中的分布及地球化学行为、异常形成原因进行了初步的讨论。相关分析表明,这些地球化学指标有密切的相关关系,反映了具有共同成因。利用热水中的钠、钾元素作为地热温标对羊八井热田地下热水的温度进行了估算。     

热田勘查中新的地球化学指标

两年来,我们利用土壤汞量测量在国内许多已知热田上进行了大量试验研究,无论高温还是中低温热田均有汞异常存在,表明汞量测量是热田勘查中一种有前景的地球化学方法。     

Regional oxygen isotope systematics of felsic volcanics; a potential exploration tool for volcanogenic massive sulphide deposits in the Iberian Pyrite Belt

Regional oxygen isotopic sytematics have been performed mainly on the felsic volcanic footwall rocks of the orebodies but also on purple schist characteristic of the hanging wall series, around two giant VMS deposits in the Spanish Iberian Pyrite Belt, Riotinto and La Zarza. As the terranes of the Iberian Pyrite Belt, these two giant deposits have been affected by the Hercynian tectono-metamorphic events, strongly modifying their geometry. About 60 and 40 samples were collected over a 10×4 km² area at Riotinto and a 3×2 km² area at La Zarza, respectively. Whole-rock powders were analysed for oxygen by CO₂-laser fluorination. At both sites, a same type of low-δ¹⁸O anomaly down to +3.6‰, well differentiated from the regional background (up to 20‰), was identified near the orebodies. The lowest δ¹⁸O values (+4 to +11‰) correspond to the chlorite hydrothermal halo, essentially restricted to the feeder zones of the orebody. Intermediate δ¹⁸O values (+9 to +15‰) correspond to the sericite hydrothermal halo, mostly developed laterally to the orebody until 0.5–1 km. The regional background (+16 to +20‰) is represented by spilitised volcanic rocks. A same kind of low anomaly, but with less contrast, was defined in purple schist in the immediate hanging wall of the orebodies. All these results demonstrate that, despite high geometrical modifications of the orebodies related to the Hercynian tectonics, oxygen isotopic anomalies recorded by volcanic host rocks during the emplacement of the mineralising hydrothermal systems are still identified. This strongly suggests that oxygen isotopic systematics could be useful to identify target areas in the Iberian Pyrite Belt, as already demonstrated on other VMS targets in the world.     

Rates of Deglaciation during the Last Glaciation and Holocene in the Cordillera Vilcanota-Quelccaya Ice Cap Region, Southeastern Perú

Moraine chronology is combined with digital topography to model deglacial rates of paleoglacier volumes in both the Huancané Valley on the west side of the Quelccaya Ice Cap and the Upismayo Valley on the northwest side of the Cordillera Vilcanota. The fastest rates of deglaciation (39×10⁻⁵ to 114×10⁻⁵ km³ yr⁻¹ and 112×10⁻⁵ to 247×10⁻⁵ km³ yr⁻¹ for each valley, respectively) were calculated for the most recent paleoglaciers, corresponding to the last few centuries. These results are consistent with observations in the Venezuelan Andes showing high rates of deglaciation since the Little Ice Age. These rates also fall within the range of 20th century rates of deglaciation measured on the Quelccaya Ice Cap (29×10⁻⁵ to 220×10⁻⁵ km³ yr⁻¹, Brecher and Thompson, 1993; Thompson, 2000). These results imply that rates of deglaciation may fluctuate significantly over time and that high rates of deglaciation may not be exclusive to the late 20th century. Equilibrium line altitude (ELA) depressions for the ice volumes of the last glaciation modeled here were computed as 230 m for the Quelccaya Ice Cap and 170 m for the Cordillera Vilcanota. Maximum ELA depressions are lower than previously published: <500 m for the Cordillera Vilcanota and <400 m for the Quelccaya Ice Cap. These lower values could imply a topographic control over paleoglacier extent.     

Geothermal waters from the Taupo Volcanic Zone,New Zealand: Li,B and Sr isotopes characterization

Chemical and isotopic data for 23 geothermal water samples collected in New Zealand within the Taupo Volcanic Zone (TVZ) are reported. Major and trace elements including Li, B and Sr and their isotopic compositions (δ⁷Li, δ¹¹B, ⁸⁷Sr/⁸⁶Sr) were determined in high temperature geothermal waters collected from deep boreholes in different geothermal fields (Ohaaki, Wairakei, Mokai, Kawerau and Rotokawa geothermal systems). Lithium concentrations are high (from 4.5 to 19.9 mg/L) and Li isotopic compositions (δ⁷Li) are homogeneous, ranging between −0.5‰ and +1.4‰. In particular, it is noteworthy that, except for the samples from the Kawerau geothermal field having slightly higher δ⁷Li values (+1.4%), the other geothermal waters have a near constant δ⁷Li signature around a mean value of 0‰ ± 0.6 (2σ, n = 21). Boron concentrations are also high and relatively homogeneous for the geothermal samples, falling between 17.5 and 82.1 mg/L. Boron isotopic compositions (δ¹¹B) are all negative, and display a range between −6.7‰ and −1.9‰. These B isotope compositions are in agreement with those of the Ngawha geothermal field in New Zealand. Lithium and B isotope signatures are in a good agreement with a fluid signature mainly derived from water/rock interaction involving magmatic rocks with no evidence of seawater input. On the other hand, Sr concentrations are lower and more heterogeneous and fall between 2 and 165 μg/L. The ⁸⁷Sr/⁸⁶Sr ratios range from 0.70549 to 0.70961. These Sr isotope compositions overlap those of the Rotorua geothermal field in New Zealand, confirming that some geothermal waters (with more radiogenic Sr) have interacted with bedrocks from the metasedimentary basement. Each of these isotope systems on their own reveals important information about particular aspects of either water source or water/rock interaction processes, but, considered together, provide a more integrated understanding of the geothermal systems from the TVZ in New Zealand.     

Geothermal mineralized scales in the pipe system of the geothermal Piancastagnaio power plant (Mt. Amiata geothermal area): a key to understand the stibnite,cinnabarite and gold mineralization of Tuscany (central Italy)

The CO₂-rich geothermal fluids produced in the Piancastagnaio geothermal field (Mt. Amiata geothermal area, Southern Tuscany, Italy) show temperatures up to 360°C and pressures of about 200 bar at depths of around 3,500 m (Giolito, Ph.D. thesis, Università degli Studi di Firenze, Italy, pp 1–147, 2005). CaCO₃- and/or SiO₂-dominated scales are deposited in the pipes leading to the pressure and atmospheric separators of the geothermal wells. High content of metastibnite and/or stibnite in both calcite and silica scales and Sb contents of up to 50 mg/L in the fluids indicate their mineralising potential. The red or black colours of the scales depend on the predominance of red metastibnite or black stibnite, respectively. In our condensation experiments, as well as during deposition of the scales, metastibnite is the first Sb₂S₃ mineral to form. In a second stage, metastibnite is transformed to stibnite. During depressurization the Hg content of geothermal fluids partitions preferentially into the gas phase, whereas Sb and As remain in the liquid phase. This separation explains the often observed areal separation of Hg and Sb mineralization. The multistage deposition of Sb in the mining district of Tuscany is due to a periodic restoration of the permeability of the ore-bearing faults by microseismic events and subsequent host rock brecciation. The still ongoing microseismic events are induced by the accumulation of high-pressure CO₂-rich fluids along faults followed by mechanical failure of the faults.     

Outburst floods from glacial Lake Missoula

The Pleistocene outburst floods from glacial Lake Missoula, known as the “Spokane Floods”, released as much as 2184 km³ of water and produced the greatest known floods of the geologic past. A computer simulation model for these floods that is based on physical equations governing the enlargement by water flow of the tunnel penetrating the ice dam is described. The predicted maximum flood discharge lies in the range 2.74 × 10⁶−13.7 × 10⁶ m³ sec⁻¹, lending independent glaciological support to paleohydrologic estimates of maximum discharge.     

Particulate-associated potentially harmful elements in urban road dusts in Xi’an,China

Sixty five urban road dust samples were collected from different land use areas of ∼240 km² in Xi’an, China. The concentrations of Ag, As, Cr, Cu, Hg, Pb, Sb and Zn were determined to investigate potentially harmful element (PHE) contamination, distribution and possible sources. In addition, the concentrations in different size fractions were measured to assess their potential impact on human health. The highest concentrations were found in the fraction with particle diameters between 80 μm and 101 μm, the finest particles (<63 μm) were not the most important carriers for Ag, As, Cd, Cr, Cu, Hg, Pb and Zn. The percentages of these elements in particles with diameters less than 63 μm (PM₆₃) and less than 101 μm (PM₁₀₁) were in the range of 7–15%, and 30–55%, respectively. Three main factors influencing element distributions have been identified: (a) industrial activities; (b) prior agricultural land use; and (c) other activities commonly found in urban areas, such as traffic, coal combustion, waste dumping, and building construction/renovation. The highest concentrations were found in industrial areas for As (20 mg kg⁻¹), Cr (853 mg kg⁻¹), Cu (1071 mg kg⁻¹), Pb (3060 mg kg⁻¹) and Zn (2112 mg kg⁻¹), and in previous agricultural areas for Ag and Hg, indicating significant contributions from industrial activities and prior agricultural activities.     

Spatial distribution of stream sediment pollution by toxic trace elements at Tourtit and Ichoumellal abandoned mining areas (central Morocco)

This study presents a diagnostic of the current state of 114 stream sediment samples by their elemental concentrations (Sb, Cd, Pb, As, Cu, Zn, Ni, Cr, and Hg), collected from Ighardayane upstream on an area of 15 km² located at the SE part of central Morocco where Tourtit and Ichoumellal, two abandoned mining sites of Stibnite, are located. Several approaches were used to model the analysis (i) enrichment factor (EF), (ii) sediment pollution index (IPS), (iii) probable effect concentration-quotients (PEC-Qs), and (iv) potential ecological risk index (PERI). Results show highly contaminated areas around the old mining sites by Sb As, Pb, and Cd. Cadmium and lead show 86.9 and 12.29% (respectively) of trace element pollution according to sediment pollution index. Twenty-eight percent of the sampled area is potentially highly toxic because of the presence of Hg, Pb, and Cd. The very similar distribution of pollution and toxicity of most analyzed trace elements may originate from the same source, which corresponds to mining wastes where we recorded the highest pollution and toxicity degrees. This environmental issue represents the combination of Tourtit and Ichoumellal anthropic sources responsible of Sb, As, Pb, and Cd release and a probable natural source of Hg “that needs a further study,” which contribute in the degradation of an aquatic ecosystem of the same area. Therefore, both ecotoxicological analysis and stream sediment quality management should be carried out to control this aquatic ecosystem toxication.     

华北平原新生界盖层地温梯度图及其简要说明

本文报道新编比例尺为1:1500000的华北平原新生界盖层地温梯度图。该图以近4000口钻井的温度资料和对地温场控制因素的分析为基础,并结合地温场数学模拟计算结果编制而成。圈定全区地温梯度G>4℃/100m及大地热流q>62mw/m²的局部地热异常区44片,总面积为25000km²,为地热能勘探、开发远景规划提供了重要的科学依据。     

根据多时相夜间MODIS LST推断的腾冲地区新生代火山岩岩浆囊分布与活动特征

腾冲火山地热区位于印度板块与欧亚板块俯冲-碰撞带的弧后活动区,是我国新生代火山-地热最为活动的地区之一.本文利用MODIS夜间月平均地表温度(Land Surface Temperature,LST)数据,计算了研究区2001～2011年132个月的月平均地表温度,圈定了地温异常区;分析了异常区年内及年际间的平均地表温度变化趋势,推测了可能的地下岩浆囊分布位置及活动特征.研究结果表明,腾冲地区现今地下可能存在3个岩浆囊:第1个位于五合-新华-蒲川-团田一带,面积约为537km2,地温异常最明显;第2个位于朗蒲-热海-马鞍山地区,面积约为226km2,地温异常次之;第3个位于马站-曲石之间,面积约为28km2,地温异常较为明显.3个地温异常区在年内的地表温度变化趋势基本一致,而且周期性明显,均在5～6月份和8～9月份出现2个温度峰.其中朗蒲-热海-马鞍山异常区的地温变化波动最大,可能反映地下岩浆囊地热系统与地表地下水系统的对流交换活动性更强.MODIS夜间月平均地表温度数据得出的结果与测震、GPS形变、He同位素比值及最大相对地热梯度等方法推测的地温异常区范围具有很好的一致性,特别是地温异常区年内温度周期性变化的发现,表明卫星热红外遥感技术应用于地热异常实时监测与研究的巨大潜力.     

Heavy metal pollution of coastal river sediments, north-eastern New South Wales, Australia: lead isotope and chemical evidence

 Heavy metal and metalloid concentrations within stream-estuary sediments (<180-μm size fraction) in north-eastern New South Wales largely represent natural background values. However, element concentrations (Ag, As, Cd, Cr, Cu, Hg, Ni, Pb, Sb, Zn) of Hunter River sediments within the heavily industrialized and urbanized Newcastle region exceed upstream background values by up to one order of magnitude. High element concentrations have been found within sediments of the Newcastle Harbour and Throsby Creek which drains into urbanized and light industry areas. Observed Pb enrichments and low ²⁰⁸Pb/²⁰⁴Pb, ²⁰⁷Pb/²⁰⁴Pb and ²⁰⁶Pb/²⁰⁴Pb ratios are likely caused by atmospheric deposition of Pb additives from petrol and subsequent Pb transport by road run-off waters into the local drainage system. Sediments of the Richmond River and lower Manning, Macleay, Clarence, Brunswick and Tweed River generally display no evidence for anthropogenic heavy metal and metalloid contamination (Ag, As, Cd, Cr, Cu, Hg, Ni, Pb, Sb, Zn). However, the rivers and their tributaries possess localized sedimentary traps with elevated heavy metal concentrations (Cu, Pb, Zn). Lead isotope data indicate that anthropogenic Pb provides a detectable contribution to investigated sediments. Such contributions are evident at sample sites close to sewage outlets and in the vicinity of the Pacific Highway. In addition, As concentrations of Richmond River sediments gradually increase downstream. This geochemical trend may be the result of As mobilization from numerous cattle-dip sites within the region into the drainage system and subsequent accumulation of As in downstream river and estuary sediments. Received: 5 September 1997 · Accepted: 4 November 1997     

A regional-scale geochemical survey of soil O and C horizon samples in Nord-Trøndelag,Central Norway: Geology and mineral potential

A highly efficient, low-density sampling strategy was employed to study the geochemical expression of geological bodies and the mineral potential on the county scale in Central Norway. Soil O and C horizon samples (N = 752) were collected in Nord-Trøndelag and parts of Sør-Trøndelag, and analysed for 53 chemical elements (Ag, Al, As, Au, B, Ba, Be, Bi, Ca, Cd, Ce, Co, Cr, Cs, Cu, Fe, Ga, Ge, Hf, Hg, In, K, La, Li, Mg, Mn, Mo, Na, Nb, Ni, P, Pb, Pd, Pt, Rb, Re, S, Sb, Sc, Se, Sn, Sr, Ta, Te, Th, Ti, Tl, U, V, W, Y, Zn, and Zr) and Pb isotopes in an aqua regia extraction. At the sample density of one site/36 km² the four metal deposits, which have been mined in the area within the last 50 years were all detected as geochemical anomalies. In addition, a number of new anomalies that may warrant follow-up surveys were found. In terms of geology the Grong–Olden Culmination is marked by a distinct ²⁰⁶Pb/²⁰⁷Pb isotope anomaly. Geochemical differences distinguish the most important belts of mafic metavolcanic lithologies in the area. Though the Fosdalen iron ore deposit is only marked in the soil O horizon, the C horizon outlines the more prominent anomalies of possibly economic interest. Climatic factors like the input of marine aerosols along the coast are clearly visible in the soil O horizon. Low-density geochemical mapping of two sample materials provides important complementing information for the interpretation of the geochemical variation in Nord-Trøndelag county.     

Linking source and sink: Evaluating the balance between onshore erosion and offshore sediment accumulation since Gondwana break-up, South Africa

The geomorphic origin and evolution of the tectonically unique interior highland of southern Africa, the Kalahari Plateau, and its flanking low-lying coastal planes, remain largely unresolved because of a lack of regional quantitative analyses of its uplift and erosion history. Here we focus on the southern Cape, South Africa and link onshore denudation, based on new apatite fission track thermochronology results, to offshore sediment accumulation, using abundant well data and a seismic reflection profile. We attempt to relate source and sink in order to resolve some first order issues concerning timing of the exhumation and development of the topographic features of southern Africa. The volume of sediment accumulated off South Africa's south coast is calculated using 173 wells and a seismic reflection profile. A total, uncompacted, sediment volume of 268,500 km³ accumulated off South Africa's south coasts since  136 Ma, in the Outeniqua and Southern Outeniqua Basins. Accumulation volumes and rates were highest in the early Cretaceous (48,800 × 10⁴ km³ at  8150 km³/Ma from  136 to 130 Ma, and 57,500 × 10⁴ km³ at 5750 km³/Ma from  130 to 120 Ma) and mid–late Cretaceous (83,700 × 10⁴ km³ at 3200 km³/Ma from  93 to 67 Ma). Volumes and accumulation rates were lowest for the early–mid-Cretaceous (47,400 × 10⁴ km³ at 1750 km³/Ma from  120 to 93 Ma) and the Cenozoic (31,200 × 10⁴ km³ at 450 km³/Ma from  67 to 0 Ma). Although our analysis shows that the accumulated volume of offshore sediments does not match the calculated volume of onshore erosion, as quantified through apatite fission track thermochronology (e.g. Tinker, J.H., de Wit, M.J., Brown, R., 2008. Mesozoic exhumation of the 439 southern Cape, South Africa, quantified using apatite fission track thermochronology. Tectonophysics, doi: 10.1016/j.tecto.2007.10.009), the timing of increased sediment accumulation closely matches the timing of increased onshore denudation. This suggests that the greatest volumes of material were transported from source to sink during two distinct Cretaceous episodes, and that the processes driving onshore denudation decreased by an order of magnitude during the Cenozoic.     

Preserved paleo-oceanic plateaus in accretionary complexes: Implications for the contributions of the Pacific superplume to global environmental change

We have reinvestigated the mid-Cretaceous plume pulse in relation to paleo-oceanic plateaus from accretionary prisms in the circum-Pacific region, and we have correlated the Pacific superplume activity with catastrophic environmental changes since the Neoproterozoic. The Paleo-oceanic plateaus are dated at 75–150 Ma; they were generated in the Pacific superplume region and are preserved in accretionary prisms. The volcanic edifice composed of both modern and paleo-oceanic plateaus is up to 10.7 × 10⁶ km² in area and 19.1 × 10⁷ km³ in volume. The degassing rate of CO₂ (0.82 − 1.1 × 10¹⁸ mol/m.y.) suggests a significant impact on Cretaceous global warming. The synchronous occurrence of paleo-oceanic plateaus in accretionary complexes indicates that Pacific superplume pulse activities roughly coincided at the Permo-Triassic boundary and the Vendian–Cambrian boundary interval. The CO₂ expelled by the Pacific superplume probably contributed to environmental catastrophes. The initiation of the Pacific superplume contributed to the snowball Earth event near the Vendian–Cambrian boundary; this was one of the most dramatic events in Earth's history. The scale of the Pacific superplume activity roughly corresponds to the scale of drastic environmental change.     

Antimony in the environment: Lessons from geochemical mapping

The distribution of Sb in a variety of sample materials, including soils, plants and surface water, was studied at different scales, from continental to local, combining published data sets with the aim of delineating the impact and relative importance of geogenic vs. anthropogenic Sb sources. Geochemical mapping demonstrates that variation is high at all scales – from the detailed scale with sample densities of many sites per km² to the continental-scale with densities of 1 site per 5000 km². Different processes govern the Sb distribution at different scales. A high sample density of several samples per km² is needed to reliably detect mineralisation or contamination in soil samples. Median concentrations are so low for Sb in most sample materials (below 1 mg/kg in rocks and soils, below 0.1 mg/kg in plants, below 0.1 μg/L in surface water) that contamination is easier to detect than for many other elements. Distribution patterns on the sub-continental to continental-scale are, however, still dominated by natural variation. Given that the geochemical background is characterised by a high variation at all scales, it appears impossible to establish a reliable single value for “good soil quality” or a “natural background concentration” for Sb for any sizeable area, e.g., for Europe. For such a differentiation, geochemical maps at a variety of scales are needed.     

Baseline geochemical mapping of Sardinia (Italy)

A total of about 20,000 stream sediment samples from about 13,000 km² were collected in Sardinia and analysed for eleven elements (Ag, Co, Cr, Cu, F, Hg, Mn, Mo, Ni, Pb, Sb and Zn) by Ente Minerario Sardo (EMS), aimed at mineral exploration. We have reutilized 16,890 samples (covering an area of 7987 km²) of the above data to compile geochemical baseline maps for all single elements as well as maps showing the regional variability of factor scores resulting from R-mode factor analysis. This type of maps has a particular relevance to environmental issues, especially in a region such as Sardinia which has been mined since pre-Roman times.