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221.
Falandysz J Gucia M Mazur A 《Journal of environmental science and health. Part. B》2007,42(6):735-740
The carpophores of Parasol Mushroom and underlying soil substrate collected from several unpolluted and spatially distant sites across Poland were examined to know content and bioconcentration potential of mercury by this species. The total mercury content of the caps of Parasol Mushroom for the particular sites ranged from 1.1 +/- 1.0 to 8.4 +/- 7.4 microg/g dry matter (total range from 0.05 to 22 microg/g dm), while in the stalks were from 0.53 +/- 0.27 to 6.8 +/- 7.1 microg/g dm (total range from 0.078 to 20 microg/g dm). A top soil layer (0-10 cm) showed baseline mercury concentration from 0.022 +/- 0.011 to 0.36 +/- 0.16 microg/g dm (total range from 0.010 to 0.54 microg/g dm). Parasol Mushroom is an effective mercury accumulator in the carpophores and bioconcentration factor (BCF) values of this element in the caps and depending on the sampling site ranged from 16 +/- 6 to 220 +/- 110 (total range from 0.52 to 470), while for the stalks were from 7.6 +/- 2.6 to 130 +/- 96 (total range from 0.52 to 340). It seems reasonable to state that tolerance (maximum allowable concentration) of the total mercury in a single cap of Parasol Mushroom at unpolluted areas should not exceed 25 microg/g dm. A value greater then 25 mu g/g dm will imply an elevated content due to site pollution problems. Nevertheless, knowledge on highly toxic methylmercury content and its fraction in the total mercury content of Parasol Mushroom is lacking. 相似文献
222.
García De Llasera MP Rodríguez-Castillo A Vera-Avila LE 《Journal of environmental science and health. Part. B》2007,42(6):615-627
The effect of organic matter on the solid-phase extraction (SPE) efficiency for pesticides belonging to different chemical groups (urea-derivatives, carbamates and triazines) and having different polarities, was simultaneously studied for the first time in pure and simulated water samples. SPE was carried out in precolumns packed with C18 silica or styrene-divinylbenzene copolymer PLRP-S phases on-line coupled to high performance liquid chromatography (HPLC) analysis. Retention factors in water (k'(W)) were estimated for 25 compounds and used for the calculation of the theoretical breakthrough volume (Vb(T)) in pure water. Experimental breakthrough volumes (Vb(E)) were first determined using purified and deionized water as the matrix for selected compounds having Vb(T) < 500 mL; then, the same water with an added humic acid sodium salt (HA) at 0.4-5.6 mg/L of dissolved organic carbon (DOC) content, was used as the matrix for compounds having VbE < 500 mL in pure water. Several polar pesticides showed negative linear or logarithmic Vb(E) curves depending on HA content; their recoveries were also determined in environmental samples having low dissolved organic carbon values, between 0.5-6.4 mg/L. A similar behavior was observed for these compounds in simulated and natural water samples, where DOC concentration and the percolated volume (Vp) mainly determine the solute recoveries values. However, the variation of recoveries as a function of DOC content could be negative or null depending on the two examined conditions (Vp lower or larger than Vb(E) in pure water). Results demonstrated that breakthrough volume must always be considered to correctly interpret the participation of dissolved humic material on the SPE efficiency of organic micropollutants in water. 相似文献
223.
Validation and global uncertainty of a gas chromatographic with mass spectrometry method for fenamidone analysis in grapes and wines 总被引:1,自引:0,他引:1
Abreu Sde M Herbert P Caboni P Cabras P Alves A Garau VL 《Journal of environmental science and health. Part. B》2007,42(7):817-822
Fenamidone is an imidazolinone fungicide recently introduced in viticulture practices. This work reports the validation and assessment of global uncertainty of a gas chromatographic with mass spectrometry method to analyze fenamidone in grapes and wines. This method consists in a simple and fast liquid-liquid extraction step followed by chromatographic determination. Limits of detection for fenamidone in grapes and wines were, respectively, 0.05 mg/kg and 0.06 mg/L, precision was below 9.4% and average recovery was 89 +/- 5%. In the concentration range from 0.05 to 1.00 mg/kg (or mg/L) of fenamidone, global uncertainty calculated following the EURACHEM/CITAC rules, and also by the Horwitz function, was below 25%. The EURACHEM/CITAC global uncertainty budget used gave lower estimates than those obtained from the Horwitz function. 相似文献
224.
Küster A Pohl K Altenburger R 《Environmental science and pollution research international》2007,14(6):377-383
Background, Goals and Scope During the last years the miniaturization of toxicity test systems for rapid and parallel measurements of large quantities
of samples has often been discussed. For unicellular algae as well as for aquatic macrophytes, fluorescence-based miniaturized
test systems have been introduced to analyze photosystem II (PSII) inhibitors. Nevertheless, high-throughput screening should
also guarantee the effect detection of a broad range of toxicants in order to ensure routinely applicable, high-throughput
measuring device experiments which can cover a broad range of toxicants and modes of action others than PSII inhibition. Thus,
the aim of this study was to establish a fast and reproducible measuring system for non-PSII inhibitors for aquatic macrophyte
species to overcome major limitations for use.
Methods A newly developed imaging pulse-amplitude-modulated chlorophyll fluorometer (I-PAM) was applied as an effect detector in short-term
bioassays with the aquatic macrophyte species Lemna minor. This multiwell-plate based measuring device enabled the incubation and measurement of up to 24 samples in parallel. The
chemicals paraquat-dichloride, alizarine and triclosan were chosen as representatives for the toxicant groups of non-PSII
herbicides, polycyclic aromatic hydrocarbons (PAHs) and pharmaceuticals and personal care products (PPCPs), which are often
detected in the aquatic environment. The I-PAM was used (i) to establish and validate the sensitivity of the test system to
the three non-PSII inhibitors, (ii) to compare the test systems with standardized and established biotests for aquatic macrophytes,
and (iii) to define necessary time scales in aquatic macrophyte testing. For validation of the fluorescence-based assay, the
standard growth test with L. minor (ISO/DIS 20079) was performed in parallel for each chemical.
Results The results revealed that fluorescence-based measurements with the I-PAM allow rapid and parallel analysis of large amounts
of aquatic macrophyte samples. The I-PAM enabled the recording of concentration-effect-curves with L. minor samples on a 24-well plate with single measurements. Fluorescence-based concentration-effect-curves could be detected for
all three chemicals after only 1 h of incubation. After 4–5 h incubation time, the maximum inhibition of fluorescence showed
an 80–100% effect for the chemicals tested. The EC50 after 24 h incubation were estimated to be 0.06 mg/L, 0.84 mg/L and 1.69
mg/L for paraquatdichloride, alizarine and triclosan, respectively.
Discussion The results obtained with the I-PAM after 24 h for the herbicide paraquat-dichloride and the polycyclic aromatic hydrocarbon
alizarine were in good accordance with median effective concentrations (EC50s) obtained by the standardized growth test for
L. minor after 7 d incubation (0.09 mg/L and 0.79 mg/L for paraquat-dichloride and alizarine, respectively). Those results were in
accordance with literature findings for the two chemicals. In contrast, fluorescence-based EC50 of the antimicrobial agent
triclosan proved to be two orders of magnitude greater when compared to the standard growth test with 7 d incubation time
(0.026 mg/L) as well as with literature findings.
Conclusion Typically, aquatic macrophyte testing is very time consuming and relies on laborious experimental set-ups. The I-PAM measuring
device enabled fast effect screening for the three chemicals tested. While established test systems for aquatic macrophytes
need incubation times of ≥ 7 d, the I-PAM can detect inhibitory effects much earlier (24 h), even if inhibition of chemicals
is not specifically associated with PSII. Thus, the fluorescence-based bioassay with the I-PAM offers a promising approach
for the miniaturization and high-throughput testing of chemicals with aquatic macrophytes. For the chemical triclosan, however,
the short-term effect prediction with the I-PAM has been shown to be less sensitive than with long-term bioassays, which might
be due to physicochemical substance properties such as lipophilicity.
Recommendations and Perspectives The results of this study show that the I-PAM represents a promising tool for decreasing the incubation times of aquatic macrophyte
toxicity testing to about 24 h as a supplement to existing test batteries. The applicability of this I-PAM bioassay on emergent
and submerged aquatic macrophyte species should be investigated in further studies. Regarding considerations that physicochemical
properties of the tested substances might play an important role in microplate bioassays, the I-PAM bioassay should either
be accompanied by evaluating physicochemical properties modeled from structural information prior to an experimental investigation,
or by intensified chemical analyses to identify and determine nominal concentrations of the toxicants tested. The chemicals
paraquat-dichloride, alizarine and triclosan were chosen as representatives for the toxicant groups of non-PSII herbicides,
PAHs and PPCPs which are often detected in the aquatic environment. Nevertheless, in order to ensure a routinely applicable
measuring device, experiments with a broader range of toxicants and samples of surface and/or waste waters are necessary.
ESS-Submission Editor: Dr. Markus Hecker (MHecker@Entrix.com) 相似文献
225.
Multiresidue analysis of pesticides in fruits and vegetables by gas chromatography-mass spectrometry
Araoud M Douki W Rhim A Najjar MF Gazzah N 《Journal of environmental science and health. Part. B》2007,42(2):179-187
A multiresidue method was assessed for the determination of several pesticides (organochlorine, organophosphorus, pyrethroids, triazole, amidine) using gas chromatography/mass spectrometry. The extraction of pesticides was carried out by liquid-liquid extraction (LLE) and solid-phase extraction (SPE) using two types of columns (CN and C18). The extracts were cleaned by the addition of florisil, the pesticides were separated by capillary column gas chromatography and detected by mass spectrometry in the electron impact mode. The extraction using C18 column provided the best results for most of the analyzed pesticides. The majority of pesticides recoveries from the four fruits and vegetables (apples, pears, tomatoes and pepper) were greater than 60%. Linearity and precision were satisfactory. The estimated limits of detection and limits of quantification ranged from 0.01 to 0.1 mg/kg and from 0.02 to 0.3 mg/kg, respectively. The proposed procedure was found to be useful for the multiresidue analyses of pesticides in agricultural products for routine monitoring programs. 相似文献
226.
Naszradi T Badacsonyi A Keresztényi I Podar D Csintalan Z Tuba Z 《Environmental monitoring and assessment》2007,134(1-3):279-285
Moss transplants of Tortula ruralis were used as active biomonitoring organisms as part of a monitoring study to assess the metals (Al, Cd, Cu, Cr, Fe, Ni, Pb, V and Zn) associated with ambient particles on mosses in Budapest, the capital town of Hungary. The moss samples were collected in a nature conservation area from a semi-arid sand grassland (Festucetum vaginatae danubiale), less than 1 month before transplantation. Moss cushions were exposed to pollution in Budapest during October–November 1993 and February–March 1994. In the study area, 16 sites were marked out as measuring sites, in accordance with the structure of the city. A similar stand was established in the Botanical Gardens of the Szent István University in Gödöll? as a control site. ICP-AES analysis of moss for metals showed the ability of Tortula ruralis to accumulate the metals under study. Control site showed lower impact in comparison to the other sites. 相似文献
227.
The Distribution and Sources of Polycyclic Aromatic Hydrocarbons in Surface Sediments Along the Egyptian Mediterranean Coast 总被引:2,自引:0,他引:2
El Nemr A Said TO Khaled A El-Sikaily A Abd-Allah AM 《Environmental monitoring and assessment》2007,124(1-3):343-359
Coastal marine sediment samples were collected from 31 sampling stations along the Egyptian Mediterranean Sea coast. All sediment
samples were analyzed to determine aliphatic and polycyclic aromatic hydrocarbons (PAHs) as well as total organic carbon (TOC)
contents and grain size analysis. Total concentrations of 16 EPA-PAHs in the sediments were varied from 88 to 6338 ng g−1 with an average value of 154 ng g−1 (dry weight). However, the concentrations of total aliphatic were varied from 1.3 to 69.9 ng g−1 with an average value of 15.6 ng g−1 (dry weight). The highest contents of PAHs were found in the Eastern harbor (6338 ng g−1), Manzala (5206 ng g−1) and El-Jamil East (4895 ng g−1) locations. Good correlations observed between a certain numbers of PAH concentrations allowed to identify its origin. The
average total organic carbon (TOC) percent was varied from 0.91 to 4.54%. Higher concentration of total pyrolytic hydrocarbons
(∑COMB) than total fossil hydrocarbons (∑PHE) declared that atmospheric fall-out is the significant source of PAHs to marine
sediments of the Egyptian Mediterranean coast. The selected marked compounds, a principal component analysis (PCA) and special
PAHs compound ratios (phenanthrene/anthracene vs fluoranthene/pyrene; ∑COMB/∑EPA-PAHs) suggest the pyrogenic origins, especially
traffic exhausts, are the dominant sources of PAHs in most locations. Interferences of rather petrogenic and pyrolytic PAH
contaminations were noticed in the harbors due to petroleum products deliveries and fuel combustion emissions from the ships
staying alongside the quays. 相似文献
228.
Kimiran-Erdem A Arslan EO Sanli Yurudu NO Zeybek Z Dogruoz N Cotuk A 《Environmental monitoring and assessment》2007,125(1-3):219-228
A hundred Enterococcus strains were isolated from seawater samples collected from coastal areas of Istanbul. Isolates were identified to the species
level using standard biochemical tests specified by Facklam and Collins. The species distribution was as follows Enterococcus
faecalis (96%), Enterococcus gallinarum (3%) and Enterococcus solitarius (1%). The resistance of bacteria to both heavy metals (zinc [Zn], iron [Fe], cadmium [Cd], chrome [Cr], cobalt [Co]) and
antibiotics (ampicillin 10 μg [AP], penicillin G 10 Units [PG], gentamycin 10 μg [GM], streptomycin 10 μg [S], chloramphenicol
10 μg [C], erythromycin 15 μg [E], kanamycin 30 μg [K], amikacin 30 μg [AK], nalidixic acid 30 μg [NA], and vancomycin 30 μg
[VA]) was evaluated. None of the strains was resistant to VA. It was found that among the 100 isolates, those that exhibit
resistance to antibiotics, particularly NA, S and K, were also resistant all the heavy metals tested. To our knowledge this
is the first report focusing on determination of resistance of environmental enterococci found in Istanbul against heavy metals
and antibiotics. Thus, combined expressions of antibiotic and heavy metal resistance may help to reinforce ecological and
epidemiological studies and to determine the role of these strains in antibiotic and heavy metal resistance dissemination. 相似文献
229.
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
230.
Demirak A 《Environmental monitoring and assessment》2007,129(1-3):189-196
In this study, the chemical composition of the rainwater in Yatağan, which is a region surrounding a coal power plant was
investigated from February to April 2002. Rainwater samples were obtained from Yatağan, located northwest of Muğla City in
Turkey. pH values and concentrations of major ions (Ca2+, Na+, K+, , , ) in the rainwater samples were analyzed. The pH varied from 5.1 to 7.9 with an average of 6.7 which was in alkaline range
considering 5.6 as the neutral pH of cloud water in equilibrium with atmospheric CO2. In the total of 30 rain events, only three events were observed with water in the acidic range (<5.6), which occurred after
continuous rains. The equivalent concentration of components followed the order: Ca2+ > > Na+ > > > K+ > H+. The anion and cation concentrations in the rainwater samples showed a high sulphate concentration (131 μEq/l), as well as
high sodium (40 μEq/l) and calcium (298 μEq/l) concentrations. These values indicate that one probable source of the high
sodium concentration is fly ash, after the coal burning process and the power plant can be effective on level concentrations in rainwater. In addition, the dust-rich local and surrounding limestone environment might have caused the
high concentration of Ca2+ in rainwater of the Yatağan Basin. Due to a large contribution of these cations to the sulphate neutralization action, the
rainwater of this region displays only a moderate acidity, which does not cause significant environmental impact. 相似文献