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1.
The marine coastal sediments from Togo have been analysed for the trace elements Cd, Cr, Cu, Ni, Pb, Sr, V, Zn and Zr to
ascertain the geo-ecological impact of dumping of phosphorite tailings into the sea. Trace element concentrations ranged from
2–44 ppm for Cd, 22–184 ppm for Cu, 19–281 ppm for Ni, 22–176 ppm for Pb, 179–643 ppm for Sr, 38–329 ppm for V, 60–632 ppm
for Zn and 18–8928 ppm for Zr. Regional distribution of trace elements in the marine environment indicates that the concentrations
of Cr, Cu, Ni, Pb, V, Sr and Zn increase seawards and along the coastal line outwards of the tailing outfall, whereas Cd and
Zr showed reversed spatial patterns. Sorting and transport of phosphorite particles by coastal currents are the main factors
controlling the distribution of particle-bound trace metals in the coastal environment. The Cd, Sr and Zn concentrations decrease
with decreasing grain size in marine coastal sediments, whereas Cr, Cu, Ni and Zn concentrations increase with decreasing
grain size. Percolation and shaking experiments were carried out in laboratory using raw phosphate material and artificial
sea water. Enhanced mobilization of Cd from phosphorites by contact with the sea water was observed.
Received: 11 May 1998 · Accepted: 20 October 1998 相似文献
2.
Heavy metals in sediments of a large, turbid tropical lake affected by anthropogenic discharges 总被引：2，自引：0，他引：2
Bottom-water data and trace metal concentration of Cu, Cr, Ni, Pb, Co, Zn, and organic matter in surficial sediment samples
from 13 sampling stations of Lake Chapala in Mexico were studied. The lake is turbid with a great amount of flocculated sediments
as a result of wind mixing, sediment re-suspension, and Lerma River discharges. Al distribution pattern in sediments was used
as an indicator of the Lerma River discharges into Lake Chapala. The highest values of Cu (33.27 ppm), Cr (81.94 ppm), Pb
(99.8 ppm), and Zn (149.7 ppm) were detected in sediments near the lake outlet. The bioavailable metal fraction is low for
all metals except Pb, which shows 65–93% of the total metal concentration in bioavailable form. The minimum energy zone in
the lake was related to organic matter concentration and was located in the SE part of the lake. An analysis of the studied
parameters shows two zones: eastern zone (fluvio-deltaic) and central-western zone (lacustrine).
Received: 9 September 1998 · Accepted: 16 November 1998 相似文献
3.
Water and bed sediment samples collected from the Damodar River and its tributaries were analysed to study elemental chemistry
and suspended load characteristics of the river basin. Na and Ca are the dominant cations and HCO3 is the dominant anion. The water chemistry of the Damodar River basin strongly reflects the dominance of continental weathering
aided by atmospheric and anthropogenic activities in the catchment area. High concentrations of SO4 and PO4 at some sites indicate the mining and anthropogenic impact on water quality. The high concentration of dissolved silica,
relatively high (Na+K)/TZ+ ratio (0.2–0.4) and low equivalent ratio of (Ca+Mg)/(Na+K) indicate that dissolved ions contribute significantly to the weathering
of aluminosilicate minerals of crystalline rocks. The seasonal data show a minimum ionic concentration in the monsoon season,
reflecting the influence of atmospheric precipitation on total dissolved solids contents. The suspended sediments show a positive
correlation with discharge and both discharge and suspended load reach their maximum value during the monsoon season. Kaolinite
is the mineral that is possibly in equilibrium with the water. This implies that the chemistry of the Damodar River water
favours kaolinite formation. The concentration of heavy metals in the finer size fraction (<37 μ m) is significantly higher
than the bulk composition. The geoaccumulation index values calculated for Fe, Mn, Zn, Ni and Cr are well below zero, suggesting
that there is no pollution from these metals in Damodar River sediments.
Received: 21 January 1998 · Accepted: 4 May 1998 相似文献
4.
Sediments from stormdrain catchments and outlets in Wellington city and sediment traps from Wellington Harbour were sampled
for trace metal content. Samples were analysed for total metal content using XRF and ICP-MS. High values of Pb and Zn were
found in stormdrain catchments and outlets, decreasing to elevated background rock levels in the harbour. Maximum values were
recorded in an inner city stormdrain catchment, with levels of Pb (4605 ppm), Cu (2981 ppm) and Zn (3572 ppm) all higher than
the biological probable effects levels (PEL). Concentrations of As, Cr, Cu, Pb, Ni and Zn concentrations in all harbour sediment
trap samples were below the PEL. The mean values for each harbour sediment trap sample can be used as an accurate historical
baseline in future studies. Stormdrain samples with high trace metal levels were close to industrial and construction sites.
The proximity of these outlets to recreational areas should be of concern to local authorities.
Received: 28 August 1997 · Accepted: 15 December 1997 相似文献
5.
Source and distribution of trace metals and nutrients in Narmada and Tapti river basins,India 总被引：2，自引：1，他引：1
The study was designed to establish the distributions of trace metals, dissolved organic carbon, and inorganic nutrients as
well as to assess the extent of anthropogenic inputs into the Narmada and Tapti rivers. Water and sediment qualities are variable
in the rivers, and there are major pollution problems at certain locations, mainly associated with urban and industrial centers.
The metal concentrations of samples of the aquatic compartments investigated were close to the maximum permissible concentration
for the survival of aquatic life, except for higher values of Cu (5–763 μg l−1), Pb (24–376 μg l−1), Zn (24–730 μg l−1), and Cr (70–740 μg l−1) and for drinking water except for elevated concentrations of metals such as Pb, Fe (850–2,060 μg l−1), Cr, and Ni (20–120 μg l−1). In general, the concentrations of trace metals in the rivers vary down stream which may affect the “health” of the aquatic
ecosystem and may also affect the health of the rural community that depends on the untreated river water directly for domestic
use. The assessment of EF, I
geo, and PLI in the sediments reveals overall moderate pollution in the river basins. 相似文献
6.
Munendra Singh 《Environmental Geology》2001,40(6):664-671
The Yamuna River sediments, collected from Delhi and Agra urban centres, were analysed for concentration and distribution
of nine heavy metals by means of atomic adsorption spectrometry. Total metal contents varied in the following ranges (in mg/kg):
Cr (157–817), Mn (515–1015), Fe (28,700–45,300), Co(11.7–28.4), Ni (40–538), Cu (40–1204), Zn (107–1974), Pb (22–856) and
Cd (0.50–114.8). The degree of metal enrichment was compared with the average shale concentration and shows exceptionally
high values for Cr, Ni, Cu, Zn, Pb and Cd in both urban centres. In the total heavy metal concentration, anthropogenic input
contains 70% Cr, 74% Cu, 59% Zn, 46% Pb, 90% Cd in Delhi and 61% Cr, 23% Ni, 71% Cu, 72% Zn, 63% Pb, 94% Cd in Agra. A significant
correlation was observed between increasing Cr, Ni, Zn, and Cu concentrations with increasing total sediment carbon and total
sediment sulfur content. Based on the Müller's geoaccumulation index, the quality of the river sediments can be regarded as
being moderately polluted to very highly polluted with Cr, Ni, Cu, Zn, Pb and Cd in the Delhi and Agra urban centres. The
present sediment analysis, therefore, plays an important role in environmental measures for the Yamuna River and the planning
of these city centres.
Received: 21 June 1999 · Accepted: 1 October 1999 相似文献
7.
Andreas G. Mueller Gregory C. Hall Alexander A. Nemchin Holly J. Stein Robert A. Creaser Douglas R. Mason 《Mineralium Deposita》2008,43(3):337-362
The Granny Smith (37 t Au production) and Wallaby deposits (38 t out of a 180 t Au resource) are located northeast of Kalgoorlie,
in 2.7 Ga greenstones of the Eastern Goldfields Province, the youngest orogenic belt of the Yilgarn craton, Western Australia.
At Granny Smith, a zoned monzodiorite–granodiorite stock, dated by a concordant titanite–zircon U–Pb age of 2,665 ± 3 Ma,
cuts across east-dipping thrust faults. The stock is fractured but not displaced and sets a minimum age for large-scale (1 km)
thrust faulting (D2), regional folding (D1), and dynamothermal metamorphism in the mining district. The local gold–pyrite
mineralization, controlled by fractured fault zones, is younger than 2,665 ± 3 Ma. In augite–hornblende monzodiorite, alteration
progressed from a hematite-stained alkali feldspar–quartz–calcite assemblage and quartz–molybdenite–pyrite veins to a late
reduced sericite–dolomite–albite assemblage. Gold-related monazite and xenotime define a U–Pb age of 2,660 ± 5 Ma, and molybdenite
from veins a Re–Os isochron age of 2,661 ± 6 Ma, indicating that mineralization took place shortly after the emplacement of
the main stock, perhaps coincident with the intrusion of late alkali granite dikes. At Wallaby, a NE-trending swarm of porphyry
dikes comprising augite monzonite, monzodiorite, and minor kersantite intrudes folded and thrust-faulted molasse. The conglomerate
and the dikes are overprinted by barren (<0.01 g/t Au) anhydrite-bearing epidote–actinolite–calcite skarn, forming a 600-m-wide
and >1,600-m-long replacement pipe, which is intruded by a younger ring dike of syenite porphyry pervasively altered to muscovite
+ calcite + pyrite. Skarn and syenite are cut by pink biotite–calcite veins, containing magnetite + pyrite and subeconomic
gold–silver mineralization (Au/Ag = 0.2). The veins are associated with red biotite–sericite–calcite–albite alteration in
adjacent monzonite dikes. Structural relations and the concordant titanite U–Pb age of the skarn constrain intrusion-related
mineralization to 2,662 ± 3 Ma. The main-stage gold–pyrite ore (Au/Ag >10) forms hematite-stained sericite–dolomite–albite
lodes in stacked D2 reverse faults, which offset skarn, syenite, and the biotite–calcite veins by up to 25 m. The molybdenite
Re–Os age (2,661 ± 10 Ma) of the ore suggests a genetic link to intrusive activity but is in apparent conflict with a monazite–xenotime
U–Pb age (2,651 ± 6 Ma), which differs from that of the skarn at the 95% confidence level. The time relationships at both
gold deposits are inconsistent with orogenic models invoking a principal role for metamorphic fluids released during the main
phase of compression in the fold belt. Instead, mineralization is related in space and time to late-orogenic, magnetite-series,
high-Mg monzodiorite–syenite intrusions of mantle origin, characterized by Mg/(Mg + FeTOTAL) = 0.31–0.57, high Cr (34–96 ppm), Ni (22–63 ppm), Ba (1,056–2,321 ppm), Sr (1,268–2,457 ppm), Th (15–36 ppm), and rare earth
elements (total REE: 343–523 ppm). At Wallaby, shared Ca–K–CO2 metasomatism and Th-REE enrichment (in allanite) link Au–Ag mineralization in biotite–calcite veins to the formation of the
giant epidote skarn, implicating a Th + REE-rich syenite pluton at depth as the source of the oxidized hydrothermal fluid.
At Granny Smith, lead isotope data and the Rb–Th–U signature of early hematite-bearing wall-rock alteration point to fluid
released by the source pluton of the differentiated alkali granite dikes. 相似文献
8.
Weisse Elster River sediment from the Leipzig Lowlands region (Saxony, Germany) is anthropogenically polluted by heavy metals.
Sediment dredged from a trap to the south of Leipzig was characterized in detail. When freshly dredged sediment contacts air,
the material turns acidic because of oxidation processes, the heavy metals become soluble and the sediment poses an environmental
risk. We are therefore developing a sediment-treatment process based on heavy metal removal by bioleaching. Leaching experiments
were carried out in suspension and in the solid bed. The heavy metals were solubilized to nearly the same extent by H2SO4 dosage (pure chemical extraction) and addition of elemental sulphur (microbial oxidation of S0 to H2SO4). With increasing dosage of the leaching agent, Zn, Cd, Ni, Cu and Cr were more and more solubilized, whereas Pb was only
dissolved in small amounts. The addition of 2% S0 is considered an optimum dosage. When 5% S0 was added to the sediment, the pH dropped to 1.76 and large amounts of undesirable compounds such as Ca, Al and Fe were solubilized.
The higher the temperature, the faster the metals were solubilized in both suspension and the solid bed. The temperature optimum
for activating the indigenous S0-oxidizing microbes of the sediment lies between 30 and 40 °C. Conditioning of freshly dredged sediment with plants makes
it suitable for solid-bed leaching; the kinetics of heavy metal solubilization from sediment conditioned for 6 months with
Phragmites australis was the same as from long-term stored sediment.
Received: 26 November 1999 · Accepted: 5 May 2000 相似文献
9.
Summary Somma-Vesuvius is an alkaline volcano whose products (pumice, scoria and lava) have alkaline (Na2O + K2O) contents between 6 and 16 wt%, Mg number <50, SiO2 59–47 wt% and MgO 0–7.8 wt% (more than 50% of the samples have a content <2 wt%). Immobile-element ratios (Th/Yb, Ta/Yb,
Ce/Yb) indicate a shoshonitic character, while the K2O content (4–10 wt%) is characteristic of ultrapotassic rocks. The behavior of selected metals is discussed by grouping them
on the basis of the stratigraphic sequence and differentiating the volcanic activity between plinian and interplinian (Rolandi et al., 1998; Ayuso et al., 1998). This allows observation of the variation within each formation from 25.000 y. BP to the last historic eruptive
cycle (1631–1944 AD). The main processes to explain the wide distribution of the data presented are fractional crystallization
of a mantle-derived magma, magma mixing, and contamination with heterogeneous lower and/or upper crust. Variation diagrams
distinguish different behavior for groups of metals: Ag (0.01–0.2 ppm), Mo (1–8.8 ppm), W (1.3–13 ppm), Pb (16–250 ppm), Sb
(0.2–2.6 ppm), Sc (0.2–61 ppm), Li (15–140 ppm) and Be (1–31 ppm) increase with increasing differentiation and tend to correlate
with the incompatible trace elements (Th, Hf, etc). Cu (10–380 ppm), Au (2–143 ppb), Co (0.7–35.1 ppm) and Fe (1.3–6.2 wt%)
decrease towards advanced stage of differentiation. Iron also identifies three magmatic groups. The ratio Fe3+/Fe2+ ranges between 0.2 and 1.8, and Fe2O3/(Fe2O3 + FeO) ranges between 0.2 and 0.8, giving rise to an oxidized environment; exceptions are in the samples belonging to the
interplinian formations: I, II, medieval and 1631–1994 AD. Fluorine ranges between 0.1 and 0.4 wt% for the complete Mt. Somma-Vesuvius
activity, except for the Ottaviano and Avellino plinian (0.8 wt%) events. Chlorine has a wider range, from 0.1 wt% to 1.6 wt%.
Mt Somma-Vesuvius has some features similar to those of mineralized alkaline magmatic systems which coincide with the transition
between subduction-related compression and extension-related to continental rifting. We infer that a prospective time for
the formation of mineralization at Mt Somma-Vesuvius was during the 1631–1944 eruptive period.
Received March 27, 2000; revised version accepted February 28, 2001 相似文献
10.
Shahid Naseem Pazeer Ahmed Syeda Sadia Shamim Erum Bashir 《Environmental Earth Sciences》2012,66(7):1831-1838
This paper is an attempt to study the geochemistry of Akra Kaur Dam (AKD) water, north of Gwadar city, southern Balochistan. Representative water samples were collected from AKD reservoir to assess the suitability of water for drinking and agriculture purposes. The major ionic composition is suggestive for freshwater. The average ionic composition demonstrate SO4 > Ca > Na > Cl > HCO3 > Mg > K. The plots on Piper diagram reflected Ca–Mg–SO4 type of water facies. High Ca/SO4 and Ca/Mg ratios revealed that the water has influence of gypsum dissolution. The negative ratio of chloro-alkaline indices indicated reverse exchange between Ca and Mg in water occurred with Na and K in rocks. The pH, electrical conductivity, total dissolved salts, Ca, Mg, Na, K, HCO3, Cl and SO4 concentrations in the dam water were below the permissible limit, however, Na and SO4 were above the desirable limit, set by the World Health Organization. Important parameters such as residue sodium carbonate, sodium percent, sodium adsorption ratio, permeability index, magnesium content and Kelley’s ratio were calculated to evaluate the suitability of water for irrigation purpose. The result were compared with standard permissible limits and found satisfactory. The health and agriculture hazards of sulphate-bearing water were also discussed. 相似文献