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1.
Seasonal variation of the concentrations of trace metals (Cd, Co, Cr, Cu, Fe, Mn, Ni, Pb and Zn) were measured by ICP-AES
in the water and sediment from the Saricay Stream, Geyik Dam and Ortakoy Well in the same basin. Comparisons between trace
metal concentrations in water and sediment in three sources (Stream, Dam and Well) were made. The concentrations of a large
number of trace metals in the water and sediment were generally higher in the Stream than in the Well and Dam, particularly
in summer. Trace metal concentration ranges in sediments of the Saricay Stream and its sources showed very wide ranges (as
mass ratio): Co: 5–476 μg g−1, Cr: 15–1308 μg g−1, Cu: 7–128 μg g−1, Fe: 1120–13210 μg g−1, Mn: 150–2613 μg g−1, Ni: 102–390 μg g−1, Pb: 0.7–31.3 μg g−1 and Zn: 18–304 μg g−1, whereas Cd was not detected. Trace metal concentration ranges found in waters were: Co: 9.5–20.7 μg L−1, Cr: 20.3–284 μg L−1, Cu: 170–840 μg L−1, Fe: 176–1830 μg L−1, Mn: 29.3–387 μg L−1, and Ni: 4.3–21.9 μg L−1. Among the trace metals studied, Cd and Zn in two seasons and Pb in winter were usually not detected or in the recommended
levels. In addition, Cd was not detected in the sediment during the winter season. The analysis of variance (one-way ANOVA)
and correlation matrix was employed for the sediment and water samples of the two field surveys (summer and winter) comparison.
The three sources showed differences in metal contents. The metal levels in sediments displayed marked seasonal and regional
variations, which were attributed to anthropogenic influences and natural processes. In the Saricay Stream, high values of
metals during the dry season showed an anthropological effect from small industry firms, e.g.: an olive mill and a dairy farm
or water dilution during summer seasons. Finally, the pollution in this basin probably originated from small industrial, low
quality coal-burned thermal power plants, and particularly agricultural and domestic waste discharges. 相似文献
2.
Heavy metal pollution of water resources can be apprehended in East Singhbhum region which is a highly mineralised zone with
extensive mining of copper, uranium and other minerals. Ten groundwater samples were collected from each site and the heavy
metal analysis was done by atomic absorption spectrophotometer. Analysis of the results of the study reveals that the concentration
of iron, manganese, zinc, lead, copper and nickel in groundwater of Bagjata mining area ranged 0.06–5.3 mg l − 1, 0.01–1.3 mg l − 1, 0.02–8.2 mg l − 1, 1.4–28.4 μg l − 1, 0.78–20.0 μg l − 1 and 1.05–20.1 μg l − 1, respectively. In case of Banduhurang mining area, the range was 0.04–2.93 mg l − 1, 0.02–1.1 mg l − 1, 0.01–4.68 mg l − 1, 1.04–33.21 μg l − 1, 1.24–18.7 μg l − 1 and 1.06–14.58 μg l − 1, respectively. The heavy metals were found to be below the drinking water standards (IS:10500 1993) except iron (0.3 mg l − 1) and manganese (0.1 mg l − 1). The hazard quotients of the heavy metals for drinking water were below 1 posing no threat due to intake of water to the
people for both the areas. 相似文献
3.
Assessment of water pollution in different bleaching based paper manufacturing and textile dyeing industries in India 总被引:3,自引:0,他引:3
Paper industries using different raw materials such as hard wood, bamboo, baggase, rice-straw and waste papers and bleaching
chemicals like chlorine, hypochlorite, chlorine dioxide, hydrogen peroxide, sulphite and oxygen were studied to estimate organic
pollution load and Adsorbable Organic Halides (AOX) per ton of production. The hard wood based paper industries generate higher
Chemical Oxygen Demand (COD) loads (105–182 kg t−1) and Biochemical Oxygen Demand (BOD) loads (32.0–72 kg t−1) compared to the agro and waste paper based industrial effluents. The bleaching sequences such as C–EP–H–H, C–E–H–H, C–E–Do–D1
and O–Do–EOP–D1 are adopted in the paper industries and the molecular elemental chlorine free bleaching sequence discharges
low AOX in the effluent. The range of AOX concentration in the final effluent from the paper industries was 0.08–0.99 kg t−1 of production. Water consumption was in the range of 100–130 m3 t−1 of paper production for wood based industries and 30–50 m3 for the waste paper based industries. Paper machine effluents are partially recycled after treatment and pulp mill black
liquor are subject to chemical recovery after evaporation to reduce the water consumption and the total pollution loads. Hypochlorite
bleaching units of textile bleaching processes generate more AOX (17.2–18.3 mg l−1) and are consuming more water (45–80 l kg−1) whereas alkali peroxide bleaching hardly generates the AOX in the effluents and water consumption was also comparatively
less (40 l kg−1 of yarn/cloth). 相似文献
4.
Manchar Lake is the largest natural freshwater lake in Pakistan. The Lake has received less fresh water in past few years.
In addition, drainage water is being discharged in the Lake through Main Nara Valley Drain (MNVD) since many years. Consequently,
concern has grown regarding the water quality of the Lake. The aim of this study was to assess the water quality of Manchar
Lake and MNVD and the objectives were to determine physiochemical properties and the concentrations of common cations and
anions as well as seven trace metals i.e. Cu, Ni, Zn, Co, Fe, Pb and Cd. The concentration of the trace metals were determined
by simultaneous preconcentration and solvent extraction using flame atomic absorption spectrometer. Results of physicochemical
parameters of Manchar Lake water samples showed mean pH 8.4 (±0.2), conductivity 2,310.3 (±581.3) μS cm−1 and hardness (as CaCO3) 213.1 (±62.3) mg l−1. Mean concentrations of cations and anions were Na 521.5 (±49.7), Cl− 413.6 (±225.7), Ca 70.7 (±12.9), Mg 56.2 (±28.9), K 17.6 (±6.5), 0.34 (±0.2) and 0.02 (±0.01) mg l−1. Mean concentrations of trace metals were Zn 15.7 (±1), Fe 12 (±3.5), Pb 9 (±2.7), Cu 8.9 (±7.7), Ni 4.3 (±3.4), Co 4 (±3.4)
and Cd 1.1 (±1) μg l−1. MNVD water samples showed mean pH 8.9 (±0.8), conductivity 1,735.7 (±567.8) μS cm−1 and hardness (as CaCO3) 184.8 (±32.4) mg l−1. In MNWD, the mean concentrations of cations and anions were Na 482.7 (±11.7), Cl− 395.7 (±271.5), Ca 79.1 (±23.5), Mg 54.2 (±28.1), K 26.2 (±21.3), NO−3 0.5 (±0.3) and 0.1 (±0.1) mg l−1. Mean concentrations of trace metals observed in MNWD water were Fe 14.9(±3.5), Cd 8.3 (±9.4), Pb 6.9 (±2.4), Cu 6.6 (±3.1),
Zn 6.2 (±1.8), Co 4.5 (±2.7), and Ni 3.5 (±2.9) μg l−1. The pH of both Manchar Lake and MNVD waters and concentration of Pb in Manchar Lake and concentration of Cd in MNVD water
were higher than the World Health Organisation’s guideline values for the drinking water quality. The water quality of Manchar
Lake was found degraded. 相似文献
5.
Citation of cyanobacterial cultures from the shores of south west coast of Gujarat, India and their relationship with sea water quality, influenced by extensive pollutant runoff is reported in this study. Intensity of pollution was evaluated by physico-chemical analysis of water. Higher load of suspended solids (60–1000 mg l−1) and nutrients (PO4
−P: 1.3–4 μmole l−1 and NO3
−N: 12.5–17.8 μmole l−1) were persistent throughout the analysis. Community structure is seen to be influenced by such persistent pollution. Twenty nine cyanobacterial species were isolated belonging to 9 genera of 4 families, with an elevated occurrence of Oscillatoria and Lyngbya species. No heterocystous cyanobacteria were isolated throughout the study. 相似文献
6.
Physico-chemical characteristics of some river and hand-dug well waters used for drinking and domestic purposes in the oil
rich Niger Delta area of Nigeria were assessed using standard methods. The concentrations of the parameters in the river water
samples ranged in the following order: pH (5.6–6.9), temperature (26.90–28.60°C), turbidity (23–63 NTU), electrical conductivity
(52–184 μs/cm), DO (5.4–7.2 mg/l), BOD (21–57 mg/l), TDS (6.0–217 mg/l), PO4
3− (0.19–1.72 mg/l), SO4
2− (25–36.8 mg/l), NO3
− (20.3–28 mg/l), Fe (6.07–15.71 mg/l), Zn (0.04–0.24 mg/l), Pb (0.01–0.17 mg/l), Ni (0.01–0.13 mg/l), Vn (0.01–0.20 mg/l)
and Hg (0.001–0.002 mg/l). The concentrations of these parameters in the hand-dug well water ranged in the following order:
pH (5.7–6.8) temperature (26–30°C), turbidity (134–171 NTU), electrical conductivity (160–340 μs/cm), DO (5.4–6.4 mg/l), BOD
(13–34 mg/l), TDS (110–190 mg/l), PO4
3− (0.84–1.84 mg/l), SO4
2− (10.6–28.1 mg/l), NO3
− (11.3–23 mg/l), Fe (13.17–16.31 mg/l), Ni (0.01–0.02 mg/l), Vn (0.01–0.04 mg/l) and Hg (0.001–0.004 mg/l). The concentrations
of BOD, turbidity, NO3
− and Fe in the water samples were above WHO and FMENV permissible limits for safe drinking water. The results suggest that
the use of such waters for drinking and domestic purposes pose a serious threat to the health of the users and calls for the
intervention of government agencies. 相似文献
7.
Presence of pesticide residues was studied in rain water during 2002 employing multi residue analysis method by gas liquid
chromatography equipped with ECD and NPD detectors and capillary columns. The presence of pesticide residues in surface aquatic
system triggered the investigation of the presence of pesticides in rain water. A total of 13 pesticides were detected in
rain water samples. Among the different groups of pesticides, organochlorines were present in the range of 0.041–7.060 ppb
with maximum concentration of p,p’-DDT up to 7.060 μg l−1. Synthetic pyrethroids were present ranging from 0.100 to 1.000 μg l−1 and organophosphates in the range of 0.050–4.000 μg l−1 showing maximum contamination with cypermethrin (1.000 μg l−1) and monocrotophos (4.000 μg l−1) of the respective groups. Almost 80% samples showed the residues above MRL of 0.5 ppb fixed for multi residues and on the
basis of single pesticide, 16–50% samples contained residues above the MRL value of 0.1 ppb. 相似文献
8.
Residues of organochlorine pesticides in water and suspended particulate matter from the Yangtze River catchment of Wuhan, China 总被引:6,自引:0,他引:6
The residues of 13 organochlorine pesticides (OCPs) in surface water and HCHs and DDTs in suspended particulate matter (SPM)
from rivers and lakes in Yangtze River catchment of Wuhan, China, were investigated. The concentration of total OCPs in surface
water varied from 1.01 to 46.49 ng l−1 (mean 10.55 ng l−1). The levels of total HCHs (ΣHCH) and total DDTs (ΣDDT) in surface water were in the range of 0.55–28.07 ng l−1 and lower than detection limit to 16.71 ng l−1, respectively, which was lower than Chinese standards on the whole. For OCPs residues in SPM, the mean levels varying from
0.20 to 34.72 ng l−1 and 0.46 to 2.72 ng l−1 for ΣHCH and ΣDDT, respectively, which ranked the relatively higher levels among Chinese studied rivers. Results from this
investigation showed that previous excessive usage of technical OCPs was the main reason for the residues of HCHs and DDTs
both in surface water and SPM, although some new sources were likely to occurred in the region. Apart from the OCPs in SPM
originated from upstream in flood season, one of the important sources of OCP residues both in water and SPM in Yangtze River
was supposed to be the inputs of its tributaries. Additionally, in situ water-SPM phase distributions of OCPs indicated that
HCHs tended totransport with water as well as DDTs was prone to combine with SPM in Yangtze River catchment of Wuhan. 相似文献
9.
Anthropogenic nexus on organochlorine pesticide pollution: a case study with Tamiraparani river basin,South India 总被引:2,自引:0,他引:2
Kumarasamy P Govindaraj S Vignesh S Rajendran RB James RA 《Environmental monitoring and assessment》2012,184(6):3861-3873
The levels of 17 organochlorine pesticides residues (OCPs) in surface water and sediments from Tamiraparani river basin, South
India were investigated to evaluate their potential pollution and risk impacts. A total of 96 surface water and sediment samples
at 12 sampling stations were collected along the river in four seasons during 2008–2009. The ΣOCP concentrations in surface
water and sediments were in the range of 0.1 to 79.9 ng l−1 and 0.12 to 3,938.7 ng g−1 dry weight (dw), respectively. Among the OCPs, the levels of dichlorodiphenyltrichloroethanes (DDTs), aldrin, dieldrin, cis-chlordane, trans-chlordane, and mirex were dominant in the sediments. The dominant OCPs in water samples are heptachlor, o,p′-DDE, dieldrin,
o,p′-DDD, and mirex, which show different source of contamination pattern among sampling seasons. The distribution pattern
of DDTs, hexachlorocyclohexane, and other OCPs in the present study shows heterogenic nature of nonpoint source of pollution.
Notable contamination of water and sediment sample that was observed in upstream (S2) 58 ng l−1 and downstream (S11) 1,693 ng g−1 dw explains agricultural and municipal outfalls, whereas frequent damming effect reduces the concentration level in the midstream.
The overall spatial–temporal distribution pattern of ΣOCP residues are illustrated by GIS package. 相似文献
10.
The toxicity characteristic leaching procedure (TCLP) is the current US-EPA standard protocol to evaluate metal leachability
in wastes and contaminated soils. However, application of TCLP to assess lead (Pb) leachability from contaminated shooting
range soils may be questionable. This study determined Pb leachability in the range soils using TCLP and another US-EPA regulatory
leaching method, synthetic precipitation leaching procedure (SPLP). Possible mechanisms that are responsible for Pb leaching
in each leaching protocol were elucidated via X-ray diffraction (XRD). Soil samples were collected from the backstop berms
at four shooting ranges, with Pb concentrations ranging from 5,000 to 60,600 mg kg−1 soil. Lead concentrations in the TCLP leachates were from 3 to 350 mg l−1, with all but one soil exceeding the USEPA non-hazardous waste disposal limit of 5 mg l−1. However, continued dissolution of metallic Pb particles from spent Pb bullets and its re-precipitation as cerussite (PbCO3) prevented the TCLP extraction from reaching equilibrium at the end of the standard leaching period (18 h). Thus, the standard
one-point TCLP test would either over- or under-estimate Pb leachability in shooting range soils. Lead concentration in the
SPLP leachates ranged from 0.021 to 2.6 mg l−1, with all soils above the USEPA regulatory limit of 0.015 mg l−1. In contrast to TCLP, SPLP leaching had reached equilibrium, with regard to both pH and Pb concentrations, within the standard
18 h leaching period, and the analytical SPLP results were in good agreement with those derived from modeling. Thus, we concluded
that SPLP is a more appropriate alternative than TCLP for assessing lead leachability in range soils. 相似文献
11.
Jun Yao WenBing Li FangFang Xia YuanGe Zheng ChengRan Fang DongSheng Shen 《Environmental monitoring and assessment》2012,184(6):3711-3720
Fly ash samples were taken from solid waste incinerators with different feeding waste, furnace type, and air pollution control
device in six cities of Zhejiang province. The solid waste incinerators there constitute one fifth of incinerators in China.
Heavy metals and polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) were analyzed in the fly ash. Moreover, the fly ash samples were extracted by toxicity
characteristic leaching procedure (TCLP). The biotoxicity of the leachate was evaluated by Chlorella pyrenoidosa. High variation and contents were found for both the heavy metals and PCDD/Fs. The contents of Zn, Cu, As, Pb, Cd, Cr, Ni,
and Hg in the fly ash samples varied from 300 to 32,100, 62.1–1175, 1.1–57, 61.6–620, 0.4–223, 16.6–4380, 1.2–94.7, and 0.03–1.4 μg g−1 dw, respectively. The total contents of 17 PCDD/Fs varied from 0.1128 to 127.7939 μg g−1 dw, and the 2,3,7,8-TeCDD toxic equivalents (TEQ) of PCDD/Fs ranged from 0.009 to 6.177 μg g−1 dw. PCDF congeners were the main contributor to the TEQ. The leachate of the fly ash showed biotoxicity to C. pyrenoidosa. A significant correlation was found between the Cd and EC50 values. Further research is required to investigate the environmental impact of the various pollutants in the fly ash. 相似文献
12.
Fernandes C Fontaínhas-Fernandes A Cabral D Salgado MA 《Environmental monitoring and assessment》2008,136(1-3):267-275
Esmoriz–Paramos lagoon is an ecosystem of great ecological importance that is located on the northwest coast of Portugal and
has been degraded as a result of industrial and anthropogenic activities. Concentrations of heavy metals (Cr, Cu, Pb and Zn)
were measured in water, sediment and in tissues (liver and muscle) of Liza saliens, which is the dominant fish from the lagoon. Comparisons between metal concentrations in water and sediments were made with
those in tissues of fish caught at the lagoon. Metals in water were quantified predominantly bound to particulate and equalled
or exceeded the limit of chronic reference values. Metal concentrations in sediments varied among sampled sites. The relative
order of concentrations was “Zn > Cu ∼ Pb > Cr” the same pattern observed for metals in water. Metals in fish tissues showed
higher concentrations in liver (262 mg Cu·Kg−1 and 89 mg Zn·Kg−1) than in muscle (<3 mg Cu·Kg−1 and 26 mg Zn·Kg−1), while Pb and Cr were not detected. These results suggest that Cu and Zn are the metals of major concern in the lagoon.
Mullet detritivorous feeding habits, bioaccumulation pattern and the high sediment metals concentrations relative to the water
suggest that sediments can be the most important source of contamination in this ecosystem. The positive relationship found
between Cu in liver and fish length demonstrates that time of exposure is a crucial factor in bioaccumulation. Condition indices
(K and HSI) in mullets from the lagoon were higher compared to mullets from sea, suggesting abnormal condition in the lagoon
population. We conclude that metals chronic exposure in the lagoon can impose considerable fish stress. The results also show
that the lagoon is an area of environmental concern. 相似文献
13.
Twelve samples each of soil and ground water were collected from paddy-wheat, paddy-cotton, sugarcane fields and tube wells
from same or near by fields around Hisar, Haryana, India during 2002–2003 to monitor pesticide residues. Residues were estimated
by GC-ECD and GC-NPD systems equipped with capillary columns for organochlorine, synthetic pyrethroid and organophosphate
insecticides. In soil, HCH (0.002–0.051 μg g−1), DDT (0.001–0.066 μg g−1), endosulfan (0.002–0.039 μg g−1) and chlordane (0.0002–0.019 μg g−1) among organochlorines, cypermethrin (0.001–0.035 μg g−1) and fenvalerate (0.001–0.022 μg g−1) among synthetic pyrethroids and chlorpyriphos (0.002–0.172 μg g−1), malathion (0.002–0.008 μg g−1), quinalphos (0.001–0.010 μg g−1) among organophosphates were detected. Dominant contaminants were DDT, cypermethrin and chlorpyriphos from the respective
groups. In water samples, HCH, DDT, endosulfan and cypermethrin residues were observed frequently. Only chlorpyriphos among
organophosphates was detected in 10 samples. On consideration of tube well water for drinking purpose, about 80% samples were
found to contain residues above the regulatory limits. 相似文献
14.
Singh SK Juwarkar AA Pandey RA Chakrabarti T 《Environmental monitoring and assessment》2008,141(1-3):201-212
The biologically treated distillery effluent (BTDE) contains intense colour, high total dissolved solids (TDS), chemical oxygen
demand (COD) and biochemical oxygen demand (BOD). These properties even after primary, secondary and tertiary treatments contain
high concentrations of TDS, COD and BOD. The paper highlights the safe disposal and treatment of BTDE on land through High
Rate Transpiration System (HRTS). HRTS is a zero discharge, low cost, high-tech method for improving the quality of BTDE for
potential reuse. The experiments conducted at bench and pilot scale showed that HRTS having coconut husk as a bedding material
could successfully treat the BTDE with a hydraulic load of 200 m3 ha−1 day−1 having BOD of 100 mg l−1 and 500 m3 ha−1 day−1 having BOD of 500 mg l−1 with average COD load of 0.686 and 2.88 ton ha−1 day−1 during the post and pre monsoon periods respectively. There was no significant increase in the organic carbon of the soil
irrigated with BTDE. The concentrations of various pollutants analyzed in the leachate were within the prescribed limit for
the drinking water sources. The colour removal was 99 to 100% and BOD and COD were possible to treat with optimum hydraulic
loading of BTDE through HRTS planted with Dendrocalamus strictus. 相似文献
15.
Ashraf W Seddigi Z Abulkibash A Khalid M 《Environmental monitoring and assessment》2006,117(1-3):271-279
In the present paper, seven heavy metals (Pb, Cd, Ni, Cu, Zn, Cr and Fe) in canned salmon, sardine and tuna fish were determined
by using atomic absorption spectroscopy. Cadmium and lead levels were determined by graphite tube AAS whereas Ni, Cu, Cr and
Fe were determined by flame AAS. Analytical results were validated by spiking the samples with various concentrations of these
metals for recovery. The metal contents, expressed in μg/g, wet weight, varied depending upon the specie studied. The levels
of Pb ranged from 0.03–1.20 μg-g−1 with an average of 0.313 μg-g−1 for salmon; 0.03–0.51 μg-g−1 with an average of 0.233 μg-g−1 for tuna and 0.13–1.97 μg-g−1 with an average of 0.835 μg-g−1 for sardines. The levels of Cd ranged from 0.02–0.38 μg-g−1 with an average of 0.161 μg-g−1 for salmon; 0.07–0.64 μg-g−1 with an average of 0.227 μg-g−1 for tuna and 0.010–0.690 μg-g−1 with an average of 0.183 μg-g−1 for sardines. Comparative evaluation of these metals in three varieties of fish showed that average concentration of lead
in sardines is about 4 times and Ni about 3 times higher as compared to tuna. Generally, the levels of these metals follow
the order sardine > salmon > tuna. The data generated in the present study compared well with the similar studies carried
out in different parts of the world. The results indicate that canned fish, in general and tuna in particular, have concentrations
within permissible limits of WHO/FAO levels for these heavy metals. Therefore, their contribution to the total body burden
of these metals can be considered as negligibly small. 相似文献
16.
Lakhani A Parmar RS Satsangi GS Prakash S 《Environmental monitoring and assessment》2007,133(1-3):435-445
Fog water samples were collected in the months of December and January during 1998–2000 at Agra, India. The samples were analyzed
for pH, major anions (F−, Cl−, SO4
2−, NO3
−, HCOO− and CH3COO−), major cations (Ca2+, Mg2+, Na+ and K+) and NH4
+ using ion chromatography, ICP-AES and spectrophotometer methods, respectively. pH of fog water samples ranged between 7.0
and 7.6 with a volume weighted mean of 7.2, indicating its alkaline characteristic. NH4
+ contributed 40%, SO4
2− and NO3
− accounted for 28%, while Ca2+, Mg2+, Na+ and K+ accounted for 16% of the total ionic concentration. The ratios of Mg2+/Ca2+ and Na+/Ca2+ in fog water indicates that 50–75% of fog water samples correspond to the respective ratios in local soil. Significant correlation
between Ca2+, Mg2+, Na+ and K+ suggests their soil origin. The order of neutralization, NH4
+ (1.4) > Ca2+ (0.28) > Mg2+ (0.12), indicates that NH4
+ is the major neutralizing species. Fog water and atmospheric alkalinity were also computed and were found to be 873 and 903 neqm−3, respectively. Both of these values are higher than values reported from temperate sites and thus indicate that at the present
level of pollutants, there is no risk of acid fog problem. The study also shows that the alkaline nature of fog water is due
to dissolution of ammonia gas and partly due to interaction of fog water with soil derived aerosols. 相似文献
17.
Achanthobrama marmid (thorn-bream) (n:24), Chondrostoma regium (nose-carp) (n:33) and Silurus glanis (wels) (n:21), and Cyprinus carpio (carp) (n:30) were collected from Sır Dam Lake in Kahramanmaraş Province. The iron (Fe), manganese (Mn), cobalt (Co), nickel
(Ni), and lead (Pb) levels were determined in the total of 108 fish samples by Atomic Absorption Spectrophotometer. The concentrations
of heavy metals were expressed as mg kg−1 wet weight of tissue. The mean Fe and Mn levels of muscle and gill of C. carpio were 0.8–5.71 and 0.30–1.96, respectively. The mean of the Fe and Mn levels of muscle and gill of A. marmid were 1.22, 5.07 and 0.38, 0.85 mg kg−1, respectively. The ranges of mean concentrations of Fe and Mn levels in muscle and gill of C. regium were 0.91, 5.61 and 0.27, 3.42 mg kg−1, respectively. The mean value of Fe in S. glanis gill was 1.03, which of Mn was 0.17 mg kg−1. Fe, Mn, Co, Ni, and Pb were not detected in the muscle of S. glanis. The mean values for Co in muscle of thorn-bream, carp, and nose-carp were 0.005, 0.01, 0.0 mg kg−1, respectively. Nickel values in the muscle were ranged between 0.38 and 1.93 in thorn-bream, 0.06 and 1.34 in carp, 0.14
and 1.89 in nose-carp, in that order. The mean Pb levels of muscle and gill of A. marmid were 0.14 and 0.29 mg kg−1, respectively. The mean values of Pb concentration of muscle and gill for C. carpio were 0.13 and 0.50 mg kg−1, respectively. In C. regium mean values for Pb in muscle and gill were 0.06 and 0.06 mg kg−1, respectively. The mean value of Pb in S. glanis gill was 0.42, ranged between 0.0–0.92 mg kg−1. 相似文献
18.
Chrastný V Vaněk A Teper L Cabala J Procházka J Pechar L Drahota P Penížek V Komárek M Novák M 《Environmental monitoring and assessment》2012,184(4):2517-2536
The soils adjacent to an area of historical mining, ore processing and smelting activities reflects the historical background
and a mixing of recent contamination sources. The main anthropogenic sources of metals can be connected with historical and
recent mine wastes, direct atmospheric deposition from mining and smelting processes and dust particles originating from open
tailings ponds. Contaminated agriculture and forest soil samples with mining and smelting related pollutants were collected
at different distances from the source of emission in the Pb–Zn–Ag mining area near Olkusz, Upper Silesia to (a) compare the
chemical speciation of metals in agriculture and forest soils situated at the same distance from the point source of pollution
(paired sampling design), (b) to evaluate the relationship between the distance from the polluter and the retention of the
metals in the soil, (c) to describe mineralogy transformation of anthropogenic soil particles in the soils, and (d) to assess
the effect of deposited fly ash vs. dumped mining/smelting waste on the mobility and bioavailability of metals in the soil.
Forest soils are much more affected with smelting processes than agriculture soils. However, agriculture soils suffer from
the downward metal migration more than the forest soils. The maximum concentrations of Pb, Zn, and Cd were detected in a forest
soil profile near the smelter and reached about 25 g kg − 1, 20 g kg − 1 and 200 mg kg − 1 for Pb, Zn and Cd, respectively. The metal pollutants from smelting processes are less stable under slightly alkaline soil
pH then acidic due to the metal carbonates precipitation. Metal mobility ranges in the studied forest soils are as follows:
Pb > Zn ≈ Cd for relatively circum-neutral soil pH (near the smelter), Cd > Zn > Pb for acidic soils (further from the smelter).
Under relatively comparable pH conditions, the main soil properties influencing metal migration are total organic carbon and
cation exchange capacity. The mobilization of Pb, Zn and Cd in soils depends on the persistence of the metal-containing particles
in the atmosphere; the longer the time, the more abundant the stable forms. The dumped mining/smelting waste is less risk
of easily mobilizable metal forms, however, downward metal migration especially due to the periodical leaching of the waste
was observed. 相似文献
19.
Concentrations of heavy metals were determined in the water column (including the sea-surface microlayer, subsurface, mid-depth
and bottom water) and sediments from Singapore’s coastal environment. The concentration ranges for As, Cd, Cr, Cu, Ni, Pb
and Zn in the seawater dissolved phase (DP) were 0.34–2.04, 0.013–0.109, 0.07–0.35, 0.23–1.16, 0.28–0.78, 0.009–0.062 and
0.97–3.66 μg L−1 respectively. The ranges for Cd, Cr, Cu, Ni, Pb and Zn in the suspended particulate matter (SPM) were 0.16–0.73, 6.72–53.93,
12.87–118.29, 4.34–60.71, 1.10–6.08 and 43.09–370.49 μg g−1, respectively. Heavy metal concentrations in sediments ranged between 0.054–0.217, 37.48–50.52, 6.30–21.01, 13.27–26.59,
24.14–37.28 and 48.20–62.36 μg g−1 for Cd, Cr, Cu, Ni, Pb and Zn, respectively. The lowest concentrations of metals in the DP and SPM were most frequently found
in the subsurface water while the highest concentrations were mostly observed in the SML and bottom water. Overall, heavy
metals in both the dissolved and particulate fractions have depth profiles that show a decreasing trend of concentrations
from the subsurface to the bottom water, indicating that the prevalence of metals is linked to the marine biological cycle.
In comparison to data from Greece, Malaysia and USA, the levels of metals in the DP are considered to be low in Singapore.
Higher concentrations of particulate metals were reported for the Northern Adriatic Sea and the Rhine/Meuse estuary in the
Netherlands compared to values reported in this study. The marine sediments in Singapore are not heavily contaminated when
compared to metal levels in marine sediments from other countries such as Thailand, Japan, Korea, Spain and China. 相似文献
20.
Hydrogeochemical characterization of contaminated groundwater in Patancheru industrial area,southern India 总被引:1,自引:0,他引:1
The groundwater is one of the most contaminated natural resources in Patancheru industrial area due to unplanned and haphazard
industrial growth and urbanization without following basic pollution control norms. The rapid industrialization initiated
in early 1970 has started showing up its after effects few years later in the form of physiochemical contamination of the
both surface and groundwater bodies of the area. It has resulted in local people being deprived of safe drinking water, plant
and aquatic life has severely affected, and situation is deteriorating over the years in the area in spite of some preventive
and remedial measures being initiated. The focus of the present study is to understand the chemical characteristics of groundwater
and geochemical processes the contaminant water is undergoing which are normally imprinted in its ionic assemblages. The water
samples collected in pre- and post-monsoon seasons from forty two groundwater and four surface water sources were analyzed
for major constituents such as Ca2+, Mg2+, Na+, K+, CO3−, HCO3−, Cl−, SO42−, NO3−, and F−, and selected samples were tested for ten important trace metals like Fe, Pb, Bi, Mn, Cr, Co, Ni, Cu, Zn, and Cd. Na+ among cations and Cl− among anions dominate the water in both the seasons where as Ca2+, HCO3−, and Cl− show significant reduction in their ionic strength in post-monsoon. The groundwater in general is of mixed type, but most
of it belong to Na+–Cl−, Na+–HCO3−, Ca2+–Mg2+–HCO3−, and Ca2+–Mg2+–Cl− facies. The Na+ and Ca2+ are in the transitional state with Na+ replacing Ca2+ and HCO3−–Cl− due to physiochemical changes in the aquifer system. The evaluation of hydrochemistry through various ionic indices, ratios,
and plots suggest that silicate–carbonate weathering, ion exchange, dissolution, and evaporation processes are responsible
for origin of the present chemical status of the groundwater which is also controlled by the contamination from extraneous
sources that could have accelerated the dissolution processes. Gibbs plots authenticate that the evolution of water chemistry
is influenced by interaction of percolating water with aquifer matrix apart from anthropogenic enrichment of elements which
get over concentrated due to evaporation. 相似文献