Magnetic properties of soils from sites with different geological and environmental settings

Measurements of magnetic susceptibility of soils, reflecting magnetic enhancement of topsoils due to atmospherically deposited magnetic particles of industrial origin, are used recently in studies dealing with outlining polluted areas, as well as with approximate determination of soil contamination with heavy metals. One of the natural limitations of this method is magnetic enhancement of soils caused by weathering magnetically rich parent rock material. In this study we compare magnetic properties of soils from regions with different geological and environmental settings. Four areas in the Czech Republic and Austria were investigated, representing both magnetically rich and poor geology, as well as point-like and diffuse pollution sources. Topsoil and subsoil samples were investigated and the effect of geology and pollution was examined. Magnetic data including mass and volume magnetic susceptibility, frequency-dependent susceptibility, and main magnetic characteristics such as coercivity (Hc and Hcr) and magnetization (Ms and Mrs) parameters are compared with heavy metal contents. The aim of the paper is to assess the applicability of soil magnetometry under different geological-environmental conditions in terms of magnetic discrimination of dominant lithogenic/anthropogenic contributions to soil magnetic signature. Our results suggest that lithology represents the primary effect on soil magnetic properties. However, in case of significant atmospheric deposition of anthropogenic particles, this contribution can be clearly recognized, independent of the type of pollution source (point-like or diffuse), and discriminated from the lithogenic one. Different soil types apparently play no role. Possible effects of climate were not investigated in this study.     

烟台港倾倒区表层沉积物重金属的富集特征及风险评价

分析了2001~2011年烟台港倾倒区表层沉积物中6种重金属的含量及时空分布特征,采用地累积指数(Igeo)和潜在生态风险指数(ERI)对重金属富集现状及潜在生态风险进行评价。结果显示：历次调查重金属含量均较低且空间分布差异小,与黄海背景值相比, Cd和Cu出现一定程度的富集。ERI评价表明2011年倾倒区潜在生态风险性较低,年际变化顺序为：2008年＞2006年＞2009年＞2011年＞2001年, Cd和Hg是近年来的主要风险因子。     

Paleo-redox depositional conditions inferred from trace metal accumulation in two Cretaceous-Paleocene organic-rich sequences from Central Egypt

Cretaceous-Paleocene organic-rich sediments in Egypt occur as an east-west trending belt extending from the Quseir-Safaga district (Red Sea) to the Kharga-Dakhla (Western Desert) region. They are associated with the Duwi Formation (phosphate-bearing) and the overlying Dakhla Formation (deeper epicontinental shale/marl). This study aims to reconstruct the paleo-redox conditions during deposition of these thermally immature organic-rich sediments using carbon-sulfur-iron systematics and trace metal proxies in two cores, one each from the Quseir and Abu Tartur areas. Paleoproductivity, based on P content, seems to have been higher in the Quseir section than in the Abu Tartur section. The Quseir section also records a relatively greater occurrence of anoxic conditions during the accumulation of these sediments than the Abu Tartur section. This difference is indicated by its markedly higher total organic carbon (TOC) content as well as higher contributions of redox-sensitive and sulfide-forming metals (Mo, U, Ni, V, and Co). A weak correlation exists between S and TOC, and a positive S intercept (>1) was observed in most of the rock units of the study sections. A high consistency between the TOC-S-Fe relations and trace metals findings was found. The uppermost Duwi and the lowermost Dakhla strata, which have the highest TOC and represent a maximum sea transgression during the Late Cretaceous, have the highest contents of redox-sensitive trace metals. The carbonate-dominated transgressive Baris and Beida members of the Dakhla Formation record relatively stronger oxygen-depleted conditions during their accumulation than others, which led to relatively higher TOC contents and redox-sensitive metal accumulations. A scenario for the environmental conditions that existed during the deposition of these organic-rich successions, based on compiled trace metals and TOC-S-Fe implications, is reconstructed here.     

胶州湾及青岛近海表层沉积物重金属赋存形态研究

2008年11月和2010年11月分别在青岛近海6个站位和胶州湾9个站位采集了表层沉积物样品,应用连续提取法分离和测定其主要成分和重金属的赋存形态。结果表明,易还原态的重金属受铁锰氧化物体系显著影响,其中镍的迁移过程基本受控于该体系,有机结合态的铬和钡迁移变化受有机质一定影响,其他形态重金属主要受外源输入影响。Pb和Cr存在显著富集,相对其他金属污染较明显。Pb的生态风险最高。胶州湾东部,尤其是李村河口附近重金属污染程度和不稳定性都最为明显。     

北戴河近岸海域表层沉积物重金属分布特征及污染评价

分析了北戴河近岸海域表层沉积物重金属含量和空间分布特征,利用修正综合指数法和潜在生态风险指数法对其污染程度进行了评价。结果表明,该区表层沉积物重金属平均含量较低,高值区主要分布在西南角和东北角河口,低值区主要分布在中部;区内重金属污染程度总体上处于较低至中等等级,污染相对明显的为人造河口、石河口和秦皇岛城区近岸海域。相对而言,Hg是主要的致污元素。     

Nereis diversicolor: an Unreliable Biomonitor of Metal Contamination in the 'Ría de Bilbao' (Spain)

Abstract. Samples of the polychaete Nereis diversicolor O.F. M üller and surficial sediments from a clean and a polluted estuary were taken during a year at monthly intervals to determine, by comparison, the range of temporal fluctuations in trace metal concentrations. Whereas metal variations in surficial sediments were more pronounced in the polluted estuary, concentrations in N. diversicolor in both estuaries showed a wide range of temporal variation that surpassed that of surficial sediments. A clear decline in all metals studied (except Mn) from polluted sediments was noted after episodes of strong rainfall. In the reference estuary the fluctuations were less pronounced. Metal body burdens in N. diversicolor from the two estuaries were usually quite similar even though total levels in sediments differed considerably, indicating a lack of worm-sediment relationship. The low level of Cu, Cr and Pb in the tissues of N. diversicolor suggest a mechanism which prevents the polychaete from being exposed to these metals in highly polluted sediments. Therefore, it is concluded that N. diversicolor cannot be considered to be an ideal biomonitor of metal contamination in the polluted Bilbao Estuary.     

Trace metal composition of colloidal organic material in marine environments

Marine colloidal material (1 kDa–0.2 μm) was isolated by cross-flow ultrafiltration followed by diafiltration and freeze-drying from surface waters of the Gulf of Mexico and the Middle Atlantic Bight (MAB), as well as from estuarine waters of Galveston Bay. Elemental characterization of isolated colloidal material included organic carbon (OC) and selected trace metal (Cu, Pb, Zn, Cd, Co, Ni, Cr, Be, Fe, Al, Mn, V, Ba, and Ti) determinations. It was found that levels of these metals in marine colloids ranged from <0.1 to 50 μg/g colloidal matter, except for Fe which generally had a concentration >120 μg/g. Most metals (Cu, Pb, Zn, Ni, Al, Mn, V, and Ti) had an average concentration >1 μg/g while concentrations of Cd, Co and Be were usually <1 μg/g. Metal concentrations (μg/g) in isolated colloids were, in general, higher in Galveston Bay than in the Gulf of Mexico, suggesting either high abundance of trace metals in estuarine waters or differences in organic matter composition. Higher colloidal metal concentrations in the MAB than in the Gulf of Mexico might be due to higher terrestrial inputs in the MAB. Colloidal metal concentrations (μg/g) were generally lower than those in average soils, continental crust and suspended particles. However, metal/aluminum ratios (Me/Al) in isolated marine colloids were significantly higher than those for average soils and continental crust. Most importantly, colloids had a metal composition and metal/OC ratio (Me/C) similar to humic substances and marine plankton, suggesting that marine colloids largely originate from planktonic sources and are composed of predominately organic components. The Me/C ratios of Galveston Bay colloids followed the sequence of Cu>Ni, Cr, Zn>Mn>Co>Pb, Cd, which is similar to the Irving–Williams order except for Mn, suggesting that the interaction of metals with marine colloids is determined by the affinity of metals for specific organic ligands.     

Evaporites,brines and base metals: Low‐temperature ore emplacement controlled by evaporite diagenesis

Salt beds and salt allochthons are transient features in most sedimentary basins, which through their dissolution can carry, focus and fix base metals. The mineralisation can be subsalt, intrasalt or suprasalt, and the salt body or its breccia can be bedded or halokinetic. In all these evaporite‐associated low‐temperature diagenetic ore deposits there are four common factors that can be used to recognise suitably prepared ground for mineralisation: (i) a dissolving evaporite bed acts either as a supplier of chloride‐rich basinal brines capable of leaching metals, or as a supplier of sulfur and organics that can fix metals; (ii) where the dissolving bed is acting as a supplier of chloride‐rich brines, there is a suitable nearby source of metals that can be leached by these basinal brines (redbeds, thick shales, volcaniclastics, basalts); (iii) there is a stable redox interface where these metalliferous chloride‐rich waters mix with anoxic waters within a pore‐fluid environment that is rich in organics and sulfate/sulfide/H₂S; and (iv) there is a salt‐induced focusing mechanism that allows for a stable, long‐term maintenance of the redox front, e.g. the underbelly of the salt bed or allochthon (subsalt deposits), dissolution or halokinetically maintained fault activity in the overburden (suprasalt deposits), or a stratabound intrabed evaporite dissolution front (intrasalt deposits). The diagenetic evaporite ‐ base‐metal association includes world‐class Cu deposits, such as the Kupferschiefer‐style Lubin deposits of Poland and the large accumulations in the Dzhezkazgan region of Kazakhstan. The Lubin deposits are subsalt and occur where long‐term dissolution of salt, in conjunction with upwelling metalliferous basin brines, created a stable redox front, now indicated by the facies of the Rote Faule. The Dzhezkazgan deposits (as well as smaller scale Lisbon Valley style deposits) are suprasalt halokinetic features and formed where a dissolving halite‐dominated salt dome maintained a structural focus to a regional redox interface. Halokinesis and dissolution of the salt bed also drove the subsalt circulation system whereby metalliferous saline brines convectively leached underlying sediments. In both scenarios, the resulting redox‐precipitated sulfides are zoned and arranged in the order Cu, Pb, Zn as one moves away from the zone of salt‐solution supplied brines. This redox zonation can be used as a regional pointer to both mineralisation and, more academically, to the position of a former salt bed. In the fault‐fed suprasalt accumulations the feeder faults were typically created and maintained by the jiggling of brittle overburden blocks atop a moving and dissolving salt unit. A similar mechanism localises many of the caprock replacement haloes seen in the diapiric provinces of the Gulf of Mexico and Northern Africa. Evaporite‐associated Pb–Zn deposits, like Cu deposits, are focused by brine flows associated with both bedded and halokinetic salt units or their residues. Stratabound deposits, such as Gays River and Cadjebut, have formed immediately adjacent to or within the bedded salt body, with the bedded sulfate acting as a sulfur source. In allochthon/diapir deposits the Pb–Zn mineralisation can occur both within a caprock or adjacent to the salt structure as replacements of peridiapiric organic‐rich pyritic sediments. In the latter case the conditions of bottom anoxia that allowed the preservation of pyrite were created by the presence of brine springs and seeps fed from the dissolution of nearby salt sheets and diapirs. The deposits in the peridiapiric group tend to be widespread, but individual deposits tend to be relatively small and many are subeconomic. However, their occurrence indicates an active metal‐cycling mechanism in the basin. Given the right association of salt allochthon, tectonics, source substrate and brine ponding, the system can form much less common but world‐class deposits where base‐metal sulfides replaced pyritic laminites at burial depths ranging from centimetres to kilometres. This set of diagenetic brine‐focusing mechanisms are active today beneath the floor of the Atlantis II Deep and are thought to have their ancient counterparts in some Proterozoic sedex deposits. The position of the allochthon, its lateral continuity, and the type of sediment it overlies controls the size of the accumulation and whether it is Cu or Pb–Zn dominated.     

Application of Geochemistry and VNIR Spectroscopy in Mapping Heavy Metal Pollution of Stream Sediments in the Takab Mining Area, NW of Iran

This study considered the possibility of using visible and near infrared (VNIR) spectral absorption feature parameters (SAFPs) in predicting the concentration and mapping the distribution of heavy metals in sediments of the Takab area. In total, 60 sediment samples were collected along main streams draining from the mining districts and tailing sites, in order to measure the concentration of As, Co, V, Cu, Cr, Ni, Hg, Ti, Pb and Zn and the reflectance spectra (350–2500 nm). The quantitative relationship between SAFPs (Depth500nm, R610/500nm, R1344/778nm, Area500nm, Depth2200nm, Area2200nm, Asym2200nm) and geochemical data were assessed using stepwise multiple linear regression (SMLR) and enter multiple linear regression (EMLR) methods. The results showed a strong negative correlation between Ni and Cr with Area2200nm, a significant positive correlation between As and Asym2200nm, Ni and Co with Depth2200nm, as well as Co, V and total values with Depth500nm. The EMLR method eventuated in a significant prediction result for Ni, Cr, Co and As concentrations based on spectral parameters, whereas the prediction for Zn, V and total value was relatively weak. The spatial distribution pattern of geochemical data showed that mining activities, along with the natural weathering of base metal occurrences and rock units, has caused high concentrations of heavy metals in sediments of the Sarough River tributaries.