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1.
Thriveni T Rajesh Kumar J Sujatha D Sreedhar NY 《Environmental monitoring and assessment》2007,128(1-3):359-368
The cyclic voltammograms of terbacil and lenacil at the hanging mercury drop electrode showed a single well defined four electron
irreversible peak in universal buffer of pH 4.0 for both compounds. The peak potentials were shifted to more negative values
on the increase of pH of the medium, implying the involvement of protons in the electrode reaction and that the proton transfer
reaction precedes the proper electrode process. The four electron single peak may be attributed to the simultaneous reduction
of carbonyl groups present in 2 and 4 in pyrimidine ring of terbacil and lenacil to the corresponding hydroxy derivative.
Based on the interfacial adsorptive character of the terbacil and lenacil onto the mercury electrode surface, a simple sensitive
and low cost differential pulse adsorptive stripping voltammetric procedure was optimized for the analysis of terbacil and
lenacil. The optimal operational conditions of the proposed procedure were accumulation potential E
acc = −0.4 V, accumulation time t
acc = 80 s, scan rate = 40 mV s−1, pulse amplitude = 25 mV using a universal buffer pH 4.0 as a supporting electrolyte. The linear concentration range was
found to be 1.5 × 10−5 to 1.2 × 10−9 mol/l and 1.5 × 10−5 to 2.5 × 10−8 mol/l with the lower detection limit of 1.22 × 10−9 and 2.0 × 10−8 mol/l. The correlation coefficient and relative standard deviation values are found to be 0.942, 0.996, 1.64% and 1.23%,
respectively, for 10 replicants. The procedure was successfully applied for determination of terbacil and lenacil in formulations,
mixed formulations, environmental samples such as fruit samples and spiked water samples. 相似文献
2.
Al-Tayar NG Nagaraja P Vasantha RA Shresta AK 《Environmental monitoring and assessment》2012,184(1):181-191
A simple, rapid, and sensitive method involving the interaction of 2,4-dinitrophenylhydrazine with imipramine hydrochloride
in presence of vanadium (V) in sulfuric acid medium has been proposed for the determination of vanadium. The purple-colored
product developed showed an absorption maximum at 560 nm and was stable for 24 h. The working curve was linear over the concentration
range of 0.1–2.8 μg ml − 1, with sensitivity of detection of 0.0124 μg ml − 1. Molar absorptivity and Sandell’s sensitivity were found to be 2.6 × 104 l/mol cm and 0.0039 μg cm − 1, respectively. The accuracy of the proposed method was assessed by Student’s t test and variance ratio F test, and the results were on par with the reported method. The method was successfully used in the determination of V in
water, human urine, soil, and plant samples, and it was free from interference by various concomitant ions. 相似文献
3.
A sensitive spectrophotometric method has been developed for determination of ametryn in agricultural samples. The proposed
method was based on reaction with pyridine and further coupling with sulfanilic acid to form a colored product. The absorbance
was measured at 400 nm with a molar absorptivity of 2.1 × 105 L mol−1 cm−1. The method shows a linear range from 0.2–20 μg mL−1 with limit of detection and limit of quantification 0.16 and 0.54 μg mL−1, respectively. The method has been successfully applied to the determination of ametryn in sugarcane juice and commercial
formulations after separation of ametryn from triazine herbicides based on solvent extraction. Recovery values were found
to be in the range of 96.0 ± 0.2% to 98.4 ± 0.1%. 相似文献
4.
Cadmium and lead were determined simultaneously in seawater by differential pulse stripping voltammetry (DPSV) preceded by
adsoptive collection of complexes with 8-hydroxyquinoline (oxine) on to a hanging mercury drop electrode (HMDE). In preliminary
experiments the optimal analytical condition for oxine concentration was found to be 2.10−5 M, at pH 7.7, the accumulation potential was −1.1 V, and the initial scannig potential was −0.8 V. The peak potentials were
found −0.652 V for Cd and −0.463 V for Pb At the 60 s accumalation time. The limit of detection (LOD) and limit of quantitatification
(LOQ) were found to be by voltammetry as 0.588 and 1.959 μg l−1 (RSD, 5.50%) for Cd and 0.931 and 3.104 μg l−1 (RSD, 4.10%) for Pb at 60 s stirred accumulation time respectively. In these conditions the most of the seawater samples
are amenable for direct voltammetric determination of cadmium and lead using a HMDE. An adsorptive stripping mechanism of
the electrode reaction was proposed. For the comparison, seawater samples were also analysed by ICP-atomic emission spectrometry
method (ICP-AES). The applied voltammetric technique was validated and good recoveries were obtained. 相似文献
5.
Kumar KS Suvardhan K Rekha D Kiran K Rao GC Jayaraj B Janardhanam K Chiranjeevi P 《Environmental monitoring and assessment》2007,129(1-3):271-276
Facile, selective and sensitive spectrophotometric method has been developed for the determination of carbosulfan in insecticidal
formulations, fortified water, food grains, agriculture wastewater and soil samples with newly synthesized reagents. The method
was based on acid and alkaline hydrolysis of the carbosulfan pesticide, and the resultant hydrolysis product of carbosulfan
was coupled with 2,6-dibromo-4-methylaniline to give a yellow color product with λ
max of 464 nm or interaction with 2,6-dibromo-4-nitroaniline to produce yellow colored product with λ
max of 408 nm or coupling with 2,4,6-tribromoaniline to form red colored product has a λ
max of 471 nm. Under optimal conditions, Beer’s law range for 2,6-dibromo-4-methylaniline (DBMA) was found to be 0.2–12.0 μg
ml−1, 0.6–16.0 μg ml−1 for 2,6-dibromo-4-nitroaniline (DBNA) and 0.4–15.0 μg ml−1 for 2,4,6-tribromoaniline (TBA). The molar absorptivity of the color systems were found to be 3.112 × 104 l mol−1 cm−1 for DBMA, 3.214 × 104 l mol−1 cm−1 for DBNA and 3.881 × 104 l mol−1 cm−1 for TBA. Sandell’s of the color reactions are 0.013 μg cm−2 (DBMA), 0.012 μg cm−2 (DBNA) and 0.011 μg cm−2 (TBA) respectively. The effect of the non-target species on the determination of carbosulfan was studied to enhance the selectivity
of the proposed methods. The formation of colored derivatives with the coupling agents is instantaneous and stable for 28,
30, and 26 h. Performance of the proposed methods were compared statistically in terms Student’s F and t-tests with the reported methods.
An erratum to this article can be found at 相似文献
6.
Reddy KJ Kumar JR Ramachandraiah C Reddy SA Reddy AV 《Environmental monitoring and assessment》2008,136(1-3):337-346
N-Ethyl-3-cabazolecarboxaldehydethiosemicarbazone (ECCT) is proposed as a new, sensitive and selective complexing reagent
for the separation and extractive spectrophotometric determination of palladium(II) at pH: 4.0 to form a yellowish orange
colored 1:1 chelate complex, which is very well extracted in to n-butanol. The absorbance was measured at a maximum wavelength,
410 nm. This method obeys Beer’s law in the concentration range 0.0–6.6 μg mL−1 and the correlation coefficient of Pd(II)-ECCT complex is 0.998, which indicates an excellent linearity between the two variables
with good molar absorptivity and Sandell’s sensitivity, 1.647 × 104 l mol−1cm−1, 6.49 × 10−3 μg cm−2, respectively. The instability constant of complex calculated from Edmond’s method, 2.724 × 10−5 was in good agreement with the value calculated from Asmus’ method 2.624 × 10−5, at room temperature. The precision and accuracy of the method is checked with calculation of relative standard deviation
(n = 5), 0.839. Edmond’s method was observed to be a more selective method in the presence of EDTA, oxalate and phosphate ions.
The method was successfully applied for the determination of Pd(II) in water samples, synthetic mixtures and hydrogenation
catalysts, employing an atomic absorption spectrometer for comparing these results. 相似文献
7.
The determination of trace amount nitrobenzene in wastewater on a hanging mercury drop electrode was studied. The determination
conditions of pH, supporting electrolyte, accumulation potential, accumulation time, and voltammetric response were optimized.
The sharp peak of the nitrobenzene was appeared at 0.05 V. The peak electric current was proportional to the concentration
of nitrobenzene in the range of 1.47 × 10−5 ∼ 1.0 × 10−3 mol/l with relative standard deviations of 3.99 ∼ 8.94%. The detection limit of the nitrobenzene in water was 5 × 10−6 mol/l. The proposed method offered low limit of determination, easy operation, the use of simple instrumentation, high sensitivity
and good reproducibility. It was applied to the determination of nitrobenzene in wastewater with an average recovery of 94.0%
∼ 105%. The proposed method provided fast, sensitive and sometimes real time detection of nitrobenzene. 相似文献
8.
Díaz A Arnedo R Céspedes-Sánchez R Devesa R Martin-Alonso J 《Environmental monitoring and assessment》2012,184(1):539-548
A performance study of diffusive gradients in thin films (DGT) and inductively coupled plasma optical emission spectrometry
(ICP-OES) was applied for the monitoring of the labile fraction of metals Al, Cd, Co, Cr, Cu, Fe, Mn, Ni, Pb and Zn, in Sant
Joan Despí Drinking Water Treatment Plant located in the South of Barcelona’s Metropolitan Area (Spain). The DWTP monitoring
protocol was optimized by working for 1 day of deployment (24 h) with the DGT device in contact with both treated and river
water matrixes. Additionally, it was demonstrated that an increase in the deployment time of 1 week did not decrease the evaluated
concentrations of the studied metals. The quality parameters of the DGT device and ICP-OES determination, such as limit of
quantification, accuracy expressed as relative error (%) and reproducibility expressed as relative standard deviation, were
evaluated. Good results were obtained for all the metals in ultrapure water; limits of quantification ranged from 1.5 μg L − 1 for cadmium to 28 μg L − 1 for zinc when deployment time of 24 h was used and from 0.2 μg L − 1 for cadmium to 4 μg L − 1 for zinc when this time was increased by 1 week. Accuracy and precisions lower than or equal to 10% were obtained at a parametric
concentration value of the metals regulated in the European Drinking Water Guidelines (98/83/EC). DGT deployment was tested
in river and treated water, and good results were obtained for Cd, Ni, Co and Zn, whereas for the other metals, a continuous
control of their metallic labile fractions was monitored. Therefore, DGT device allows the continuous monitoring of the labile
metal species in a drinking water treatment plant. 相似文献
9.
Kanchi S Saraswathi K Venkatasubba Naidu N 《Environmental monitoring and assessment》2011,183(1-4):531-543
Two novel and facile ligands ammonium piperidine dithiocarbamate (Amm Pip-DTC) and ammonium morpholine dithiocarbamate (Amm Mor-DTC) were synthesized for the development of rapid and cost effective catalytic hydrogen current technique to analyze cobalt(II) in the presence of NH(4)Cl-NH(4)OH at pH 7.8 and 8.4 with Amm Pip-DTC and Amm Mor-DTC. These ligands produce catalytic hydrogen currents with Co(II) at peak potentials -1.24 V and -1.44 V vs. SCE respectively. Quantitative experimental conditions are developed by studying effect of pH, supporting electrolyte (NH(4)Cl), ligand and metal ion concentrations and effect of adverse ions on peak height to improve the sensitivity, selectivity and detection limits of the catalytic hydrogen current technique and compared it in terms of Student's t test and variance ratio f test with differential pulse polarographic (DPP) method. The developed technique was applied for the analysis of cobalt(II) in various water samples, agricultural materials and pharmaceuticals and the results obtained are in good agreement with the DPP data. 相似文献
10.
Kumar KS Suvardhan K Rekha D Kiran K Jayaraj B Janardhanam K Chiranjeevi P 《Environmental monitoring and assessment》2007,127(1-3):67-72
Facile, selective and sensitive spectrophotometric method has been developed for the determination of bendiocarb in its insecticidal
formulations, fortified water, food grains, agriculture wastewater and agriculture soil samples with prepared reagents. The
method was based on alkaline hydrolysis of the bendiocarb pesticide, and the resultant hydrolysis product of bendiocarb was
coupled with 2,6-dibromo-4-methylaniline to give a yellow color product with λmaxof457 nmorcouplingwith2, 6−dibromo−4−nitroanilinetoproducearedcoloredproductwithλmax
of474~nmorcouplingwith2, 4, 6−tribromoanilinetoformorangeredcoloredproducthasaλmax
of465 nm.Underoptimalconditions, Beer'slawrangefor2, 6−dibromo−4−methylaniline(DBMA)wasfoundtobe0.6−−14.0~μgmL
-1, 0.8−−10.0 μgmL
-1
for2, 6−dibromo−4−nitroaniline(DBNA)and0.4−−10.0 μgmL
-1
for2, 4, 6−tribromoaniline(TBA).Themolarabsorptivityofthecolorsystemswerefoundtobe4.126~×~104
lmol
-1 cm
-1
forDBMA, 3.254×104
l~mol
-1 cm
-1
forDBNAand2.812×104
lmol
-1 cm
-1
forTBA.Sandell'softhecolorreactionsare0.018 μgcm
-2(DBMA), 0.052 μgcm
-2(DBNA)and0.065 μgcm
-2$ (TBA) respectively. The effect of the non-target species on the determination of bendiocarb was studied. The formation of
colored derivatives with the coupling agents is instantaneous and stable for 18 h, 30 h, and 12 h. Performance of the proposed
methods were compared statistically in terms Student's F and t-tests with the reported methods. 相似文献
11.
To assess the potential for treated wastewater irrigation to impact levels of fecal indicator bacteria (FIB) and salinity
in irrigated soils, levels of Escherichia coli, Enterococcus, and environmental covariates were measured in a treated wastewater holding pond (irrigation source water), water leaving
the irrigation system, and in irrigated soils over 2 years in a municipal parkland in Arizona. Higher E. coli levels were measured in the pond in winter (56 CFU 100 mL−1) than in summer (17 CFU 100 mL−1); however, in the irrigation system, levels of FIB decreased from summer (26 CFU 100 mL−1) to winter (4 CFU 100 mL−1), possibly related to low winter water use and corresponding death of residual bacteria within the system. For over 2 years,
no increase in FIB was found in irrigated soils, though highest E. coli levels (700 CFU g−1 soil) were measured in deeper (20–25 cm) soils during summer. Measurements of water inputs vs. potential evapotranspiration
indicate that irrigation levels may have been sufficient to generate bacterial percolation to deeper soil layers during summer.
No overall increase in soil salinity resulting from treated wastewater irrigation was detected, but distinct seasonal peaks
as high as 4 ds m−1 occurred during both summers. The peaks significantly declined in winter when surface ET abated and more favorable water
balances could be maintained. Monitoring of seasonal shifts in irrigation water quality and/or factors correlated with increases
and decreases in FIB will aid in identification of any public health or environmental risks that could arise from the use
of treated wastewater for irrigation. 相似文献
12.
A method for the preconcentration of the total chromium based on coprecipitation with cerium (IV) hydroxide is proposed for
determination of chromium by flame atomic absorption spectrometry. Different factors including carrier element amount, pH,
sample volume and matrix ion effects for the precipitation were examined. The detection limit of the total chromium (k = 3, N = 15) was 0.18 μg l−1. The presented method was applied for the determination of chromium in the wastewater samples from Kayseri and Nigde Organized
Industrial Region-Turkey and in drinking water from our laboratory, Kayseri with satisfactory results (relative standard deviations
below 8%, recoveries 95%). The analytical results obtained by the proposed method for certified copper sample was in good
agreement with the certified value. 相似文献
13.
Remeteiová D Rusnák R Kucanová E Fióová B Ružičková S Fekete I Horváth M Dirner V 《Environmental monitoring and assessment》2012,184(2):1121-1130
In this work are presented results of the complex study of two significant solid environmental samples: gravitation dust sediments
(industrial pollutants, potential source of risk elements input to soils) and soils (component of the environment, potential
source of risk elements input to food web). The first phase of this study was focused on the study of the significant chemical
properties (phase composition, content of organic and inorganic carbon) of the dust and soil samples. In the second phase,
the fractionation analysis was used on the evaluation of the mobility of chosen risk elements (Cu, Ni, Pb, Zn) in the studied
samples. The single-step extractions were applied in the order of the isolation of the element forms (fractions), with different
mobilities during defined ecological conditions by utilization of the following reagents: 1 mol dm − 3 NH4NO3 for isolation of the “mobile” fraction, 0.05 mol dm − 3 ethylenediaminetetraacetic acid and 0.43 mol dm − 3 CH3COOH for isolation of the “mobilizable” fraction, and 2 mol dm − 3 HNO3 for isolation of all releasable forms. On the basis of the results obtained in this study, it is possible to state that different
origins and positions of solid environmental samples in the environment reflect in different chemical properties of their
matrix. The different properties of the sample matrix result in different mobilities of risk elements in these kinds of samples.
The fractionation analysis with single-step extraction for isolation element fractions is the method most suitable for easy
checking of environmental pollution and for evaluation of risk elements cycle in the environment. 相似文献
14.
An experiment was conducted under laboratory conditions to investigate the effect of two systemic herbicides viz., pendimethalin
and quizalofop, at their recommended field rates (1.0 kg and 50 g active ingredient ha − 1, respectively) on the growth and activities of non-symbiotic N2-fixing bacteria in relation to mineralization and availability of nitrogen in a Typic Haplustept soil. Both the herbicides, either singly or in a combination, stimulated the growth and activities of N2-fixing bacteria resulting in higher mineralization and availability of nitrogen in soil. The single application of quizalofop
increased the proliferation of aerobic non-symbiotic N2-fixing bacteria to the highest extent while that of pendimethalin exerted maximum stimulation to their N2-fixing capacity in soil. Both the herbicides, either alone or in a combination, did not have any significant difference in
the stimulation of total nitrogen content and availability of exchangeable NH4
+ while the solubility of NO3
− was highly manifested when the herbicides were applied separately in soil. 相似文献
15.
Bhatia A Pathak H Jain N Singh PK Tomer R 《Environmental monitoring and assessment》2012,184(5):3095-3107
Conventional blanket application of nitrogen (N) fertilizer results in more loss of N from soil system and emission of nitrous
oxide, a greenhouse gas (GHG). The leaf color chart (LCC) can be used for real-time N management and synchronizing N application
with crop demand to reduce GHG emission. A 1-year study was carried out to evaluate the impact of conventional and LCC-based
urea application on emission of nitrous oxide, methane, and carbon dioxide in a rice–wheat system of the Indo-Gangetic Plains
of India. Treatments consisted of LCC scores of ≤4 and 5 for rice and wheat and were compared with conventional fixed-time
N splitting schedule. The LCC-based urea application reduced nitrous oxide emission in rice and wheat. Application of 120 kg
N per hectare at LCC ≤ 4 decreased nitrous oxide emission by 16% and methane by 11% over the conventional split application
of urea in rice. However, application of N at LCC ≤ 5 increased nitrous oxide emission by 11% over the LCC ≤ 4 treatment in
rice. Wheat reduction of nitrous oxide at LCC ≤ 4 was 18% as compared to the conventional method. Application of LCC-based
N did not affect carbon dioxide emission from soil in rice and wheat. The global warming potential (GWP) were 12,395 and 13,692 kg CO2 ha−1 in LCC ≤ 4 and conventional urea application, respectively. Total carbon fixed in conventional urea application in rice–wheat
system was 4.89 Mg C ha−1 and it increased to 5.54 Mg C ha−1 in LCC-based urea application (LCC ≤ 4). The study showed that LCC-based urea application can reduce GWP of a rice–wheat
system by 10.5%. 相似文献
16.
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
17.
In a comprehensive program of environmental radioactivity survey in South Caspian region,137Cs inventories in soil has been measured at more than 50 sites in the Iranian northern province of Guilan. This has been the
first wide-range survey of soil radionuclide inventories in the narrow band sensitive ecosystem of south Caspian shore. Radioactivity
measurements were carried out using HPGe gamma-spectrometry system. The activity concentration of 137Cs in surface soil exhibits a mean value of 17.6 ± 9.4 Bq kg−1, with a range of 2.3–41.7 Bq kg−1. In many sites, split-level sampling method has been applied down to a depth of 20 cm. There were found generally two profiles.
Most profiles exhibit a negative exponential distribution, while others revealed a clear subsurface peak in 5–10-cm layer.
Cesium deposition in the study area has been estimated to be in the range of 0.38–2.9 kBq m−2 with a mean value of 1.7 kBq m−2. Distribution patterns of 137Cs concentration levels and deposition values have been estimated using Kriging interpolation method. Observed hotspots in
deposition pattern coincide with areas of higher precipitation. 相似文献
18.
Cheong YW Yim GJ Ji SW Kang SS Skousen J 《Environmental monitoring and assessment》2012,184(1):503-513
The objective of this study was to assess the changes in mine water quality as an underground mine flooded from July 2005
to October 2008. The effect of air injection with a blower into the water was used to evaluate the potential to convert ferrous
to ferric iron and to provide in situ treatment and precipitation. Mine flooding averaged 31 cm/day with a linear shape until
November 2007, when it flattened out due to outflow. During flooding, mine water pH remained around 6, but Eh shifted from
200 to −150 mV. After the mine water level stabilized, contents of elements such as Fe and SO4 tended to decrease as time passed. Air was injected by diffusers (150 L/min/each) at three different depths of 2, 3, and
5 m below the water level in the shaft. Dissolved oxygen eventually increased to 4 or 5 mg/L depending on the depth of the
diffusers. Aeration caused conversion of ferrous iron to ferric iron and about 30 mg/l of iron was removed from the mine water.
Therefore, air injection shows potential as a semi-active treatment or part of conventional treatment to precipitate iron
in the mine pool. 相似文献
19.
Modeling Phosphate Influence on Arsenate Reduction Kinetics by a Freshwater Cyanobacterium 总被引:1,自引:0,他引:1
Arsenic speciation in natural surface-water systems can be highly impacted through biological processes that result in non-thermodynamically
predicted species to dominate the system. In laboratory experiments, arsenate reduction by a freshwater cyanobacterium exhibited
saturation kinetics increasingly inhibited by elevating solution phosphate concentrations. Approximately 100% arsenate reduction
occurred by days 4, 7, and 10 in the low (0.35 μm), middle (3.5 μm), and high (35 μm) phosphate treatments, respectively,
with maximum arsenate reduction rates ranged from 0.013 μmol As g C−1 day−1 in the high-phosphate treatment to 0.398 μmol As g C−1 day−1 in the low-phosphate treatment. Saturation kinetic models were utilized to evaluate the impact of cell growth and arsenate-phosphate
uptake competition on arsenate reduction rates by the cyanobacterium. Results showed reduced arsenicals dominate arsenic speciation
once growth reached steady state, indicating reduced arsenicals may dominate natural systems, even when considering conservatively
high, abiotic arsenic reoxidation. 相似文献
20.
Aerosol samples for dry deposition and total suspend particulates (TSP) were collected from August to November of 2003 in central Taiwan. Ion chromatography was used to analyze the related water-soluble ionic species (Cl−, NO3
−, SO4
2−, Na+, NH4
+, K+, Mg2+ and Ca2+). The results obtained in this study indicated that the ambient air particulate mass concentrations in the daytime period (averaged 975.4 μg m−3) were higher than the nighttime period (averaged 542.1 μg m−3). And the daytime dry deposition fluxes (averaged 58.12 μg m−2 sec−1) were about 2.2 times as that of nighttime dry deposition fluxes (averaged 26.54 μg m−2 sec−1) of the downward dry deposition. The average values downward and upward of dry deposition fluxes for the weekend period were almost higher than the weekday period for either daytime or nighttime period. Furthermore, the average daytime dry deposition fluxes (averaged 26.37 μg m−2 sec−1) were also about 2.3 times as that of nighttime dry deposition fluxes (averaged 11.52 μg m−2 sec−1). Moreover, the results also indicate that SO4
2− and Ca2+ have higher average composition for total suspended particulates in the daytime period while Ca2+, SO4
2−, and Na+ have the higher average composition for total suspends particulates in the nighttime period. 相似文献