Study of galvanic interactions between pyrite and chalcopyrite in a flowing system: implications for the environment

When galvanic interactions between pyrite and chalcopyrite occur in solution, pyrite, with the higher rest potential, acts as a cathode and is protected whereas chalcopyrite, with the lower rest potential, acts as an anode and its oxidation is increased. In this work a three-electrode system was used to investigate the corrosion current density and mixed potential of a galvanic cell comprising a pyrite cathode and a chalcopyrite anode in a flowing system. The results showed that with increasing concentration of ferric ion in the solution, with increasing acidity, and with increasing flow rate of the solution, the corrosion current density increased and the mixed potential of the galvanic cell became more positive. These experimental results are of direct significance to the control of environmental pollution in mining activity. By using the galvanic model, mixed potential theory, and the Butler–Volmer equation, the experimental results were explained theoretically.     

开放体系下方铅矿和黄铁矿之间原电池反应的实验研究

金属硫化物矿物之间的原电池反应对于酸性矿山排水的形成、硫化物矿床的次生富集作用、地球电化学勘探以及湿法冶金过程等都有很重要的影响。通过改变溶液中氧化剂组分F e3 的浓度、pH值、溶液的流动状况以及溶液的盐度(如N a2SO4的浓度),采用精密的电流计和电位计,对作为阳极的黄铁矿与作为阴极的方铅矿所形成的原电池反应的电流密度和整个原电池的混合电位进行研究,结果表明:溶液中[F e3 ],pH值以及溶液的流动状况对黄铁矿和方铅矿之间原电池反应的影响很大,而溶液的盐度对反应的影响不是很显著。实验还发现,当黄铁矿电极表面存在微小裂纹时,其电极电位可降低至同条件下方铅矿的电极电位以下。这一实验结果在混合电位理论和Bu tler-V o lm er方程中得到了理论上的解释。     

Galvanic interaction between galena and pyrite in an open system

1IntroductionMost sulfide minerals in nature have perfect con-ductivity and possess semiconducting properties.Gal-vanic corrosion may occur when two sulfide mineralswith different potentials are connected together in thesolution.The mineral with the highe…     

Emarat carbonate-hosted Zn–Pb deposit, Markazi Province, Iran: A geological, mineralogical and isotopic (S, Pb) study

The Emarat deposit, with a total proved reserve of 10 Mt ore grading 6% Zn and 2.26% Pb, is one of the largest Zn–Pb deposits in the Malayer–Esfahan belt. The mineralization is stratabound and restricted to Early Cretaceous limestones and dolomites. The ore consists mainly of sphalerite and galena with small amounts of pyrite, chalcopyrite, calcite, quartz, and dolomite. Textural evidence shows that the ore has replaced the host rocks and thus is epigenetic.Sulfur isotopes indicate that the sulfur in sphalerite and galena has been derived from Cretaceous seawater through thermochemical sulfate reduction. Sulfur isotope compositions of four apparently coprecipitated sphalerite–galena pairs suggest their precipitation was under equilibrium conditions. The sulfur isotopic fractionation observed for the sphalerite–galena pairs corresponds to formation temperatures between 77 °C and 168 °C, which agree with homogenization temperatures of fluid inclusions.Lead-isotope studies indicate that the lead in galena has been derived from heterogeneous sources including orogenic and crustal reservoirs with high ²³⁸U/²⁰⁴Pb and ²³²Th/²⁰⁴Pb ratios. Ages derived from the Pb-isotope model give meaningless ages, ranging from Early Carboniferous to future. It is probable that the Pb-isotope model ages that point to an earlier origin than the Early Cretaceous host rocks are derived from older reservoirs in the underlying Carboniferous or Jurassic units, either from the host rocks or from earlier-formed ore deposits within these units.This research and other available data show that the Emarat Zn–Pb deposit has many important features of Mississippi Valley-type (MVT) lead–zinc deposits and thus we argue that it is an MVT-type ore deposit.     

The distribution of heavy metals in an abandoned mining area; a case study of Strauss Pit, the Drake mining area, Australia: implications for the environmental management of mine sites

Surface water samples from the Drake mining area show elevated metal concentrations, notably cadmium, iron and zinc. A detailed study of a sphalerite /quartz vein from Strauss Pit and chalcopyrite and pyrite from the Adeline mine and Strauss Pit indicate that micro-scale analyses of ores are necessary for environmental management of mine sites. Analyses show that Cd is elevated, up to 2.1 % by weight, and is associated with sphalerite, replacing Zn, or to a lesser extent replacing Pb within small galena grains. High concentrations of Cu are also associated with the Strauss Pit ore as small chalcopyrite grains along the margins of the sphalerite vein, within the central quartz zone of the vein system, and as replacement rims on sphalerite grains. Chalcopyrite from the Adeline mine area, is by comparison, metal poor, but still contains elevated heavy metal concentrations. Whereas, pyrite and chalcopyrite, from Strauss Pit have variable heavy metal concentrations, with chalcopyrite from within sphalerite veins having higher Cd and Zn concentrations than chalcopyrite distal to the veins. Cadmium and other heavy metals within the ores are mobilised during sulphide weathering and enter the drainage network; precipitation of secondary oxidation minerals act as temporary stores for many heavy metals. The complexity of the mineral and heavy metal associations at Strauss Pit suggest that a detailed knowledge of these associations and distributions within ore bodies, and associated waste rocks, are needed by environmental managers of mine sites because the presence of havy metals may greatly affect the decision making process, and management strategies employed. Received; 14 July 1999 · Accepted: 17 August 1999     

Galvanic interactions between galena–sphalerite and their reactivity

The galvanic effect between the main associated mineralogical phases in a mineral sphalerite concentrate was evaluated using an alternative methodology. Comparative voltammetric studies were performed between high purity galena mineral (94.65%) and sphalerite concentrate (content of 78.11% sphalerite, ZnS; 13.64% galena, PbS; 0.57% chalcopyrite, CuFeS₂; 0.41% cadmium sulfide, CdS; and 0.11% arsenopyrite, FeAsS) using carbon paste electrodes (CPE) in order to identify galvanic interactions that affect their reactivity. The electrolyte was an aqueous solution of 0.1 M NaNO₃ (pH 6.5). The results showed that, in sphalerite concentrate, the electrochemical reactivity of the galena was diminished and displaced to more positive potentials with respect to the high purity galena mineral response. This behavior can be attributed to the galvanic protection offered by the sphalerite on the galena, thereby avoiding its free oxidation. On the other hand, sphalerite oxidation was diminished by the formation of a passive products film that is dissolved to more positive potentials which provokes oxidation of other minerals like CuFeS₂, (Zn,Cd)S and FeAsS present in a minor proportion in the sphalerite concentrate.     

Assessment of contamination load on water,soil and sediment affected by the Kongjujeil mine drainage,Republic of Korea

Environmental pollution in the Kongjujeil mine creek was determined on the basis of physicochemical and mineralogical properties for various kinds of waters, soils, precipitates and sediments collected in August and December 1998. The hydrochemistry of water is characterized by an enrichment in concentrations of Ca ²⁺, Si, alkali ions, NO ₃ ^- and Cl ^- in ground and surface water, where relatively the mine waters are significantly enriched in Ca ²⁺+Mg ²⁺, Al, heavy metals and SO ₄ ^2- concentrations. The mine waters have lower pH (3.24) and higher EC (613 µS/cm) compared with those of ground and surface water. The ranges of dD and d ¹⁸O values (SMOW) in the water are -50.2 to -61.6‰ and -7.0 to -8.6‰. Using a computer code, the saturation indices of albite, calcite and dolomite in the mine water show that it is undersaturated, and has progressively evolved toward the equilibrium state. Ground and surface water are nearly saturated. The gibbsite, kaolinite and smectite are supersaturated in the surface and groundwater. Geochemical modeling shows that mostly toxic metals exist largely in the form of metal sulfates and free metals in mine water. These metals in the surrounding fresh water could be formed of carbonate or hydroxide complex ions. Minerals within the soil and sediment near the mining area were partly variable consisting of quartz, mica, alkali feldspar, plagioclase, chlorite, vermiculite, berthierine and clay minerals. The separated heavy minerals, soil and sediment are composed of some pyrite, arsenopyrite, chalcopyrite, sphalerite, galena, malachite, goethite and various hydroxide minerals. Some potentially toxic elements (As, Cd, Cu, Pb, Sb and Zn) are found in extremely high concentrations in the surface soils in the vicinity of the mine. The enrichment index of heavy metals in sediment and surface soil of the mine drainage was very severe, while it was not so great in the cultivated soil.     

Supergene sulphides and related minerals in the supergene profiles of VHMS deposits from the South Urals

The mineralogy and structure of the supergene profile in recently-exploited volcaniс hosted massive sulphide (VHMS) deposits of Cyprus, Uralian and Kuroko type in the South Urals, Russia, have been studied. Specific subzones enriched in secondary sulphides and associated minerals have been distinguished in residual pyrite and quartz–pyrite sands at the Gayskoye, Zapadno-Ozernoye, Dzhusinskoye and Alexandrinskoye deposits. Besides minerals which are common to the cementation subzones (covellite, chalcocite and acanthite), non-stoichiometric colloform and framboidal pyrite, pyrite–dzharkenite, pyrrhotite-like and jordanite-like minerals, metacinnabar, sphalerite, selenium-enriched tetrahedrite and unidentified As-, Sb sulphosalts of Pb or Hg and Ag, sulphur-bearing clausthalite, naumannite and tiemannite were also found. Secondary sulphide minerals in VHMS deposits of the South Urals region are characterized by light sulphur isotope compositions (− 8.1 to − 17.2‰). Superposition of the advanced oxidation of colloform pyrite, an enrichment in impurities (sphalerite, galena, and tennantite) from the primary ores, stagnant water conditions, an elevation of the water table during oxidation, and bacterial activity led to supergene concentrations of the base metals as sulphide, selenides or sulphosalts.     

Bulk compositions of intimate intergrowths of chalcopyrite and sphalerite and their genetic implications

To determine the bulk chemical compositions of chalcopyrite containing starlike sphalerite and sphalerite including dotlike chalcopyrite, specimens from various types of ore deposits in Japan were used for modal and electron microprobe analyses. According to the analytical results, most of the measured zinc contents in chalcopyrite containing starlike sphalerite are less than 0.8 at%, corresponding to the maximum solubility of zinc in chalcopyrite as determined experimentally at 400°C. However, specimens from the Maruyama deposit in the Tsumo mine contain 1.2–1.4 at% Zn, which are within the solubility limit of an intermediate solid solution (ISS) above 400°C. It is therefore concluded that starlike sphalerite in chalcopyrite are exsolution products derived from primary chalcopyrite solid solution and/or zincic ISS. Measured copper contents in sphalerite including dotlike chalcopyrite yield considerably higher values, i.e., 1.5–6.0 at%, which exceed the solubility limits of copper in sphalerite solid solution as determined experimentally. This result suggests that not all the chalcopyrite dots were exsolved from sphalerite, but that most of them are the product of some other mechanisms.     

Geochemical approach to estimate the quality of water entering abandoned underground coalmines

Geochemical modeling was employed to estimate the chemistry of water infiltrating into abandoned underground flooded and unflooded coalmines of the Uniontown syncline, Fayette County, Pennsylvania. This was done to help evaluate factors governing the long-term evolution of coalmine discharge water quality in the Uniontown syncline area. The subsurface structure and lithology was delineated using borehole, mine shaft, and stratigraphic information. Hydrogeologic analyses indicated that most of the recharge to mine voids occurs in the zones of shallow overburden cover of less than 20 m in thickness. The water–rock contact period in the recharge areas of the overburden was estimated to be 5 days or greater for the flooded mines, and a day or less for the unflooded mines. Flow-through reaction-path models were applied to the topsoil and shale–sandstone lithological units identified in the recharge areas. The model predicted water entering the flooded mines at a pH of 6.65, alkalinity of 6.92 mequiv. l^–1 and a total sulfate concentration of 7.33 mM, and the unflooded mines at a pH of 6.68, alkalinity of 6.99 mequiv. l^–1 and a total sulfate concentration of 3.08 mM. The model predictions for the flooded and unflooded mines are consistent with groundwater data from the study site, indicating the usefulness of this approach in evaluating the contribution of overburden chemistry to the evolution of mine discharge quality.     

硫化矿原电池效应研究现状

硫化矿原电池效应普遍存在于金属硫化物矿山、硫化矿的人工开采与利用过程中,在浮选、湿法冶金、生物冶金、地球化学过程、重金属离子污染和酸性矿山排水的污染治理方面有重要作用,已引起高度重视。本文综述了硫化矿原电池反应原理、电化学研究方法及其在浮选、湿法冶金、生物冶金、地球化学过程、重金属离子污染和酸性矿山排水的污染与治理上的影响和应用现状。指出建立天然硫化物矿物原电池地球化学,从源头上实现消除或减弱硫化矿原电池效应导致的重金属离子和酸性矿山排水环境污染,将成为今后原电池效应在地学的重要研究方向。     

Hydrothermal evolution of the Sar-Cheshmeh porphyry Cu–Mo deposit, Iran: Evidence from fluid inclusions

The Sar-Cheshmeh porphyry Cu–Mo deposit is located in Southwestern Iran (65 km southwest of Kerman City) and is associated with a composite Miocene stock, ranging in composition from diorite through granodiorite to quartz-monzonite. Field observations and petrographic studies demonstrate that the emplacement of the Sar-Cheshmeh stock took place in several pulses, each with associated hydrothermal activity. Molybdenum was concentrated at a very early stage in the evolution of the hydrothermal system and copper was concentrated later. Four main vein Groups have been identified: (I) quartz+molybdenite+anhydrite±K-feldspar with minor pyrite, chalcopyrite and bornite; (II) quartz+chalcopyrite+pyrite±molybdenite±calcite; (III) quartz+pyrite+calcite±chalcopyrite±anhydrite (gypsum)±molybdenite; (IV) quartz±calcite±gypsum±pyrite±dolomite. Early hydrothermal alteration produced a potassic assemblage (orthoclase-biotite) in the central part of the stock, propylitic alteration occurred in the peripheral parts of the stock, contemporaneously with potassic alteration, and phyllic alteration occurred later, overprinting earlier alteration. The early hydrothermal fluids are represented by high temperature (350–520 °C), high salinity (up to 61 wt% NaCl equivalent) liquid-rich fluid inclusions, and high temperature (340–570 °C), low-salinity, vapor-rich inclusions. These fluids are interpreted to represent an orthomagmatic fluid, which cooled episodically; the brines are interpreted to have caused potassic alteration and deposition of Group I and II quartz veins containing molybdenite and chalcopyrite. Propylitic alteration is attributed to a liquid-rich, lower temperature (220–310 °C), Ca-rich, evolved meteoric fluid. Influx of meteoric water into the central part of the system and mixing with magmatic fluid produced albitization at depth and shallow phyllic alteration. This influx also caused the dissolution of early-formed copper sulphides and the remobilization of Cu into the sericitic zone, the main zone of the copper deposition in Sar-Cheshmeh, where it was redeposited in response to a decrease in temperature.     

A stable isotope and fluid inclusion study of the Qaleh-ZariCu–Au–Ag deposit, Khorasan Province, Iran

The Qaleh-Zari copper deposit, located in South Khorasan in the Central Lut region of Iran, is a polymetallic vein deposit with major amounts of Cu, Au, Ag and minor amounts of Pb, Zn and Bi. Mineralization occurs in a series of NW–SE trending fault planes and breccia zones in Paleogene andesitic to basaltic volcanic rocks. Argillization, sericitization and propylitization characterize alteration halos bordering mineral veins. The main ore minerals are chalcopyrite, pyrite, galena and sphalerite, with quartz, calcite and minor chlorite as the main gangue phases. Microthermometric measurements of fluid inclusions in cogenetic quartz indicate homogenization temperatures between 160 and 300 °C and salinities from 1 to 4 wt% NaCl equiv. Boiling occurred in the mineralising fluids at 160–1000 m below the paleo-water table at pressures of approximately 15−80 bar at various stages in the formation of the ore body. The wide range of pressures and temperatures reflects the multi-stage nature of the mineralization at Qaleh-Zari. The δ¹⁸O values in quartz (relative to SMOW) and δ³⁴S values in chalcopyrite and galena (relative to CDT) range from 6.5 to 7.5‰ and 0.0–1.5‰ (mean: 7.0‰), respectively. At 300 °C, calculated fluid δ¹⁸O values are close to 0‰. These data suggest a magmatic origin for sulfur and a surficial origin for the mineralizing fluid. Mineralization at Qaleh-Zari is interpreted as epithermal and low-sulfidation in style and was probably related to a deep-seated magmatic system. Ore deposition was the result of boiling, cooling and pressure reduction.     

Gold occurrence in Central Italy—the Ponte San Pietro mineralization

Gold mineralization related to a sulphide-bearing quartz vein within Triassic phyllites has been identified in a former study of an abandoned Cu–Zn–Pb mine in southern Tuscany–northern Latium. The vein-hosted mineral assemblage includes pyrite, sphalerite, chalcopyrite, galena, arsenopyrite, and tetrahedrite; the gold content reaches up to 20 ppm. The mineralization was related to fluids characterised by moderate temperatures and moderate salinities (5–15% NaCl equivalent) and represents the highest grade of Au in the ore deposits of southern Tuscany. The difference in the estimated values of Te of primary, L+V, pseudo-secondary L+V, secondary L+V fluids inclusions reflects different components present in the solutions.Based on these results one can conclude that euhedral quartz and pyrite deposition was related to fluids having variable salinity and chemical components.The origin of gold in Ponte San Pietro (PSP) deposit may be related to leaching of metapelites/phyllites derived from pelitic rocks containing some amount of sulphur-bearing organic matter; it is worthy noting that quartz–marcasite bearing lenses, interstratified in Triassic phyllites, contain significant amount of visible gold. The Co, Ni, Mn, as well as the δ³⁴S data, suggest a different origin for the phyllite-hosted marcasite, the PSP quartz-vein hosted pyrite, and for gold occurrences.     

A sulfur isotope study of volcanogenic massive sulfide deposits of the Eastern Black Sea province,Turkey

Kuroko-type massive sulfide deposits of the Eastern Black Sea province of Turkey are related to the Upper Cretaceous felsic lavas and pyroclastic rocks, and associated with clay and carbonate alteration zones in the footwall and hangingwall lithologies. A complete upward-vertical section of a typical orebody consists of a stringer-disseminated sulfide zone composed mainly of pyrite and chalcopyrite; a massive pyrite zone; a massive yellow ore consisting mainly of chalcopyrite and pyrite; a black ore made up mainly of galena and sphalerite with minor amounts of chalcopyrite, bornite, pyrite and various sulfosalts; and a barite zone. Most of the deposits in the province are associated with gypsum in the footwall or hangingwall. The paragenetic sequence in the massive ore is pyrite, sphalerite, chalcopyrite, bornite, galena and various sulfosalts, with some overlap between the mineral phases. Massive, stringer and disseminated sulfides from eight kuroko-type VMS deposits of the Eastern Black Sea province have a ³⁴S range of 0–7 per mil, consistent with the ³⁴S range of felsic igneous rocks. Sulfides in the massive ore at Madenköy (4.3–6.1 per mil) differ isotopically from sulfides in the stringer zone (6.3–7.2 per mil) suggesting a slightly increased input of H₂S derived from marine sulfate with time. Barite and coarse-grained gypsum have a ³⁴S range of 17.7–21.5 per mil, a few per mil higher than the ³⁴S value of contemporaneous seawater sulfate. The deposits may, therefore, have formed in restricted basins in which bacterial reduction of sulfate was taking place. Fine-grained, disseminated gypsum at Kutlular and Tunca has ³⁴S values (2.6–6.1 per mil) overlapping those of ore sulfides, indicating sulfide oxidation during waning stages of hydrothermal activity.     

Silver and silver-bearing minerals at the Um Samiuki volcanogenic massive sulphide deposit, Eastern Desert, Egypt

The Um Samiuki Zn–Cu–Pb–Ag mineralisation, south Eastern Desert, Egypt is hosted by felsic volcanic rocks which form part of the 712-Ma-old, east-west-trending Shadli Volcanic Belt. Two major occurrences of massive sulphides are present at the top of rhyolitic breccia in the Western and Eastern mine areas. In each occurrence, a bornite-bearing zone is overlain by a pyrite-chalcopyrite-bearing zone and underlain by a disseminated, Cu-depleted zone. In the massive sulphide ore, sphalerite, chalcopyrite, pyrite, galena, bornite and tetrahedrite–tennantite are major minerals, whereas arsenopyrite, pyrrhotite, molybdenite and magnetite are accessory phases. Covellite and digenite are common secondary minerals. Bornite, tetrahedrite–tennantite and covellite contain high amounts of silver (averages of 1.97, 1.39 and 1.82 wt% respectively). Based on mineralogical balance calculations, bornite and covellite accommodate 80% of silver in the Um Samiuki deposit. Ag was incorporated in the crystal structure of the early-crystallised copper sulphides and sulphosalts and silver minerals. The temperature, sequential precipitation of the fluids and the structure of the crystallising phases control the distribution of silver. Post-depositional deformation and metamorphic processes caused liberation, remobilisation and redeposition of silver within the massive sulphides.Editorial handling: D. Lentz     

On the natural floatability of sulfides

A system is presented in which an atmosphere containing less than 10^?6 mole fraction oxygen and water containing less than 5 ppb oxygen can be maintained. Flotation of chalcocite, chalcopyrite, galena, pyrite and sphalerite in this system reveals that these minerals are naturally floatable under these conditions.     

Partition of cadmium and manganese between coexisting sphalerite and galena from some Japanese epithermal deposits

Sphalerites from Japanese epithermal Pb-Zn vein-type deposits, namely, Yatani, Oizumi and Hosokura, contain 2900–3400 ppm cadmium and 760–2100 ppm manganese. And galenas from the same deposits contain cadmium and manganese 19.2–26.9 ppm and 7.8–218.3 ppm, respectively. The temperatures, evaluated from the partition of cadmium between coexisting sphalerite and galena, are consistent within a total range of 150°C at maximum within an individual deposit. No systematic change with depth can be observed at the Shoko-hi vein, Hosokura mine and Hompi vein, Yatani mine. In several samples, the temperatures obtained from the partition of cadmium have been compared with those obtained from sulfur isotope fractionations. Iron content in sphalerite coexisting with pyrite indicates that the deposition of ore minerals at these deposits may have taken place from ore-forming solutions in which H₂S or HS^– was the predominant dissolved sulfur species, and the solutions may have been free from in situ oxidation or reduction.     

Sulphur‐isotope study of the massive sulphide orebody at Woodlawn,New South Wales

³⁴S/³²S ratios have been measured in a suite of samples from the stratabound, volcanogenic massive sulphide deposit at Woodlawn, N.S.W. ³⁴S values for the sulphides vary as follows: in the ore horizon, pyrite +6.7 to +9.2%. (mean +8.1‰), sphalerite +5.2 to +8.6‰. (mean +6.9‰), chalcopyrite +6.4 to +7.0‰ (mean +6.7‰) and galena +2.8 to +5.5‰ (mean +4.4‰); in the vein mineralization, the host volcanics—pyrite +8.7 to +11.4%. (mean +9.8‰), sphalerite +7.8 to + 10.3‰ (mean +9.2‰), chalcopyrite; +8.8 to +10.1‰ (mean +9.2‰) and galena +6.9 to +7.2‰ (mean +7.1‰). Barite from the upper ore horizon levels has an isotopic composition of +30.0‰, consistent with its having originated from Silurian ocean sulphate. The general order of ³⁴S enrichment in the sulphides is pyrite > chalcopyrite ～ sphalerite > galena. Isotopic fractionations in the systems galena/sphalerite/pyrite and chalcopyrite/pyrite indicate an equilibration temperature of 275–300°C. This temperature is considered to represent that of sulphide deposition.     

Chemistry of rainwaters in the south Pacific area of Russia

On the south-eastern edge of Russia, the chemical composition of rainwater is controlled by sea salts, terrestrial material, as well as volcanic (Kuril islands volcanic area) and anthropogenic emissions, mostly in the southern part of the area. The predominant major ions of the Primorye, Sakhalin and the Kuril Islands rainwaters were respectively HCO₃⁻–SO₄²⁻, Ca–Na, and of Cl–Na. Concentration of trace elements changes within 1–2 orders of magnitude but some difference in the distribution of the elements between continental and island rainwater is found. The concentration of the chemical elements in the particulate fraction varies from < 10% to 90% of the total concentration (dissolved + particulate) with the following distribution: Tl, Na, Ca, Sr, Zn, Cd (< 10%)–Be, Th, Bi, Rb, U, K, Sc (10–20%)–Cu, Mn, Mg, Mo, Se, Ba, Ni, As, Ag, Cs, Co, Y, Ga, V (20–50%)–Sb, Pb, Ge, Cr, Fe, Al (50–90%).The concentration of elements of the particulate fraction of the rainwater usually is significantly different from concentrations in the crust, including both higher and lower concentrations. The terrestrial contribution to dissolved elements was evaluated and follows the decreasing order: Fe > K, Mg, Ca > Ba, Sr > Na (65–1%). Close order was found for total (dissolved and solid) concentrations. Sea salt contribution to dissolved element concentration in the rainwater decrease in the following order: Cl, Mg > K, SO₄ > Ca > HCO₃⁻, Ba, Fe (78–0.1%). Calculation of anthropogenic and volcanic inputs for two ions (Cl⁻ and SO₄²⁻) shows that anthropogenic inputs for the Vladivostok and Yuzno-Sakhalinsk cities can be evaluated as 15–20% of Cl⁻ and up to 80–90% of SO₄²⁻. Volcanic components in the Kuril Islands, where anthropogenic inputs are absent, can reach up to 76% of SO₄²⁻ and 36% of Cl⁻.