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A new fluorescent sensor based on the BODIPY fluorophore and the polyamide receptor for Pb(2+) was designed and synthesized. The sensor is highly selective for Pb(2+) over relevant competing metal ions, and sensitive to ppb levels of Pb(2+). It features the most sensitive probe to date for Pb(2+) ions in water.

The exponential increase in fossil energy production from Devonian-age shale in the Northeastern United States has highlighted the management challenges for produced waters from hydraulically fractured wells. Confounding these challenges is a scant availability of critical water quality parameters for this wastewater. Chemical analyses of 160 flowback and produced water samples collected from hydraulically fractured Marcellus Shale gas wells in Pennsylvania were correlated with spatial and temporal information to reveal underlying trends. Chloride was used as a reference for the comparison as its concentration varies with time of contact with the shale. Most major cations (i.e., Ca, Mg, Sr) were well-correlated with chloride concentration while barium exhibited strong influence of geographic location (i.e., higher levels in the northeast than in southwest). Comparisons against brines from adjacent formations provide insight into the origin of salinity in produced waters from Marcellus Shale. Major cations exhibited variations that cannot be explained by simple dilution of existing formation brine with the fracturing fluid, especially during the early flowback water production when the composition of the fracturing fluid and solid-liquid interactions influence the quality of the produced water. Water quality analysis in this study may help guide water management strategies for development of unconventional gas resources.

A highly selective and efficient single molecular FRET based sensor has been developed for the ratiometric detection of Fe(3+) in aqueous samples and live cells.

Background: The reduced activity of 11β hydroxysteroid dehydrogenase type 2 (11βHSD2) contributes to elevated blood pressure (BP) in clinical syndromes, but its effect on BP in the physiologic range is unclear., Objectives: We examined the association of 11βHSD2 activity with BP in healthy children independent of known BP-related dietary and other factors and determined whether the diet-dependent acid load may constitute a dietary factor related to BP., Design: We conducted a cross-sectional analysis in 267 healthy children (age range: 4-14 y) who provided a 24-h urine sample, a parallel 3-d weighed dietary record, and 1-3 BP measurements ±1.5 y around the urine collection. The ratio of urinary free cortisone to cortisol measured by using a radioimmunoassay was used as an index for 11βHSD2. Urinary net acid excretion and the urinary and dietary potential renal acid load (PRAL) were used to predict the diet-dependent acid load. The PRAL was calculated as the sum of major mineral nonbicarbonate anions minus the sum of mineral cations. Sex-, age- and height-independent SD scores (SDSs) of systolic and diastolic BP were used as outcomes in linear regression analyses., Results: 11βHSD2 was inversely associated with systolic BP SDSs in basic models and in analyses adjusted for body size, maternal BP, breastfeeding, and dietary intakes of total energy, salt, and fruit and vegetables (P = 0.03). In models that included indexes of dietary acid load instead of fruit and vegetables, all 3 acid-load biomarkers were significantly (P = 0.006-0.02) directly related to systolic BP., Conclusion: A lower 11βHSD2 activity and higher dietary acid load may independently contribute to higher systolic BP in healthy children.

In this contribution we present an innovative way to easy, fast, and highly sensitive analyses by CE with ESI-MS detection. The new method is designed to be applied to ESI-compatible electrolytes (e.g. ammonium acetate) and offers advanced tuning of selectivity conditions within a wide range of analyte mobilities. We use a full capillary ITP format to provide powerful on-line analyte stacking at the ITP boundary all the way to detection and introduce the model of extended ITP where a controlled concentration of the leading ion is added to the terminating zone. Such systems preserve all properties of an ITP system and the velocity of the stacking ITP boundary can be tuned by the composition of both the leading and terminating zone. In this way, the system properties can be controlled flexibly and the mobility window of stacked analytes can be tailored to actual needs. The presented theory and the newly defined concept of zone-related boundary mobility allow easy assessment of system selectivity using simple diagrams. We demonstrate the model and its potential on the example of simple acidic cationic systems composed of only two substances (ammonium and acetate) including the example of thiabendazole analysis with a detection limit of 10(-10) M (20 ng/L) and its determination in orange juice by direct sampling after filtration, selective stacking by a tuned extended ITP system, and ESI-MS detection., (© 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

A novel fluorescent chemical sensor for the highly sensitive and selective determination of Fe(3+) ions in aqueous solutions is prepared. The iron sensing system was prepared by incorporating 5-(8-hydroxy-2-quinolinylmethyl)-2,8-dithia-5-aza-2,6-pyridinophane (L) as a neutral Fe(3+)-selective fluoroionophore in the plasticized PVC membrane containing sodium tetraphenylborate as a liphophilic anionic additive. The response of the sensor is based on the strong fluorescence quenching of L by Fe(3+) ions. At pH 5.5, the proposed sensor displays a calibration curve over a wide concentration range from 6.0 × 10(-4) to 1.0 × 10(-7) M, with a relatively fast response time of less than 2 min. In addition to a high stability and reproducibility, the sensor shows a unique selectivity toward Fe(3+) ion with respect to common coexisting cations. The proposed fluorescence optode was applied to the determination of iron(III) content of straw of rice, spinach and different water samples. The fluorescent sensor was also used as a novel probe for Fe(3+)/Fe(2+) speciation in aqueous solution., (Copyright © 2012 Elsevier B.V. All rights reserved.)

A water-soluble biocompatible aziridine-based biosensor with pendant anthracene units was synthesized by radicalar polymerization of N-substituted aziridines in supercritical carbon dioxide. The binding ability of the sensor towards a series of metal ions was examined by comparing the fluorescence intensities of the solutions before and after the addition of 100 equivalents of a solution of the metal ion chloride salt. A fast, simple and highly optical sensitive dual behavior, "off-on" and "on-off" response, was observed after the biosensor was exposed to the metal cations in aqueous solution. Zinc presented the highest fluorescence enhancement (turn-on) and copper presented the highest fluorescence quenching (turn-off). The response time was found to be instantaneous and the detection limit was achieved even in the presence of excess metal cation competitors. By using immunofluorescence microscopy it was also shown that oligoaziridine acts as an "on-off" probe through highly sensitive (detection limit of 1.6nM), selective and reversible binding to copper anions under physiologic conditions using living Human Fibroblast cells. The stoichiometry for the reaction of the biosensor with Cu(2+) was determined by a Job plot and indicates the formation of an oligoaziridine-Cu(2+) 1:2 adduct., (Copyright © 2012 Elsevier B.V. All rights reserved.)

In order to train scientist field investigators after terrorist attacks, the laboratory of the Prefecture de Police of Paris simulated a suicide bombing attack in a bus. After collection of the residues, analyses were carried out to determine the composition of the original explosive charge. This article focuses on the combined use, for the first time, of three new capillary electrophoresis methods for the determination of inorganic anions and cations, and carbohydrates in two representative extracts. Capillary electrophoresis appears as an effective tool to identify and quantify the compounds in real extracts and is fully complementary to chromatographic methods., (Copyright © 2012 Elsevier B.V. All rights reserved.)

A novel and highly sensitive method for the determination of some heavy metals in skin whitening cosmetics creams using multiwalled carbon nanotubes MWCNTs as solid phase extraction sorbent for the preconcentration of these heavy metals prior to their determination by inductively coupled plasma atomic emission spectrometry is described. Different practical parameters have been thoroughly investigated and the optimum experimental conditions were employed. The developed method was then applied for the determination of arsenic, bismuth, cadmium, mercury, lead and titanium in samples of skin whitening cosmetics. The detection limits under these conditions for As, Bi, Cd, Pb, Hg and Ti were 2.4, 4.08, 0.3, 2.1, 1.8, and 1.8 ng·mL-1, respectively. The relative standard deviations (RSDs) were found to be less than 2.0%. For validation, a certified reference material of NIST SRM 1570a spinach leaves was analyzed and the determined values were in good agreement with the certified values. The recoveries for spiked samples were found to be in the range of 89.6-104.4%.

Unlabelled: Size-segregated distribution of ambient particulate matter (PM) was determined using a micro-orifice uniform deposition impactor (MOUDI) and a nano-MOUDI in southern Taiwan. Eleven water-soluble ionic species including six anions (NO3-, SO4(2-), Cl-, F-, NO2-, Br-) and five cations (NH4+, Na+, K+, Ca2+, Mg2+) for particulate inorganic ions and five gaseous pollutants (i.e., HNO2, HNO3, HCl, SO2, NH3) were analyzed during episode and non-episode periods. The particulate mass concentration was about 30 microg/ m3 higher at night than during the day, and it reached 162 microg/m3 during the episode periods. The difference was mainly attributable to the particle size of 0.1-2.5 microm. Nitrate, sulfate, ammonium, and chloride ions were the dominant inorganic ions in PM. HONO and NH3 concentrations were high at night; in contrast, HNO3, HCl, and SO2 were high during the day. The equivalent ratio of {[NO3-] + 2 [SO4(2-)}/[NH4+] was about 0.98 and revealed a high correlation between {[NO3-] + 2[SO4(2-)]} and [NH4+] that clearly pointed to ammonium neutralization or condensation of ammonium nitrate and ammonium sulfate in PM0.32. The precursor gases and ionic species in different particle sizes did not reveal a strong correlation, which could be attributed to the complex of source emissions, atmospheric reactions and meteorological parameters in the area., Implications: Size-segregated distribution and chemical compositions of atmospheric aerosols play important roles in their visibility reduction, health effects, and toxicity in urban areas. Inorganic ionic species are major constituents in particulate matter, except carbonaceous chemicals. In this work, the compositions of water-soluble ions in particulate matter and acid/base gaseous pollutants (such as HNO2, HNO3, HCl, SO2, NH3) were determined during the day and at night during episode and non-episode periods from 2006 to 2007 in southern Taiwan.

Herein, we describe indirect UV detection-ion-exclusion/cation-exchange chromatography (IEC/CEC) on a weakly acidic cation-exchange resin in the H(+)-form (TSKgel Super IC-A/C) using sulfosalicylic acid as the eluent. The goal of the study was to characterize the peaks detected by UV detector. The peak directions of analyte ions in UV at 315 nm were negative because the molar absorbance coefficients of analyte anions and cations were lower than that of the sulfosalicylic acid eluent. Good chromatographic resolution and high signal-to-noise ratios of analyte ions were obtained for the separations performed using 1.1 mM sulfosalicylic acid and 1.5 mM 18-crown-6 as the eluent. The relative standard deviations (RSDs) of the peak areas ranged from 0.6 to 4.9%. Lower detection limits of the analytes were achieved using indirect UV detection at 315 nm (0.23 - 0.98 μM) than those obtained with conductometric detection (CD) (0.61 - 2.1 μM) under the optimized elution conditions. The calibration curves were linear in the range from 0.01 to 1.0 mM except for Cl(-), which was from 0.02 to 2.0 mM. The present method was successfully applied to determine common inorganic ions in a pond water sample.

The purpose of this research is to use a simple method to prepare magnetic modified biomass with good adsorption performances for cationic ions. The magnetic modified biomass was prepared by two steps: (1) preparation of pyromellitic dianhydride (PMDA) modified biomass in N, N-dimethylacetamide solution and (2) preparation of magnetic PMDA modified biomass by a situ co-precipitation method under the assistance of ultrasound irradiation in ammonia water. The adsorption potential of the as-prepared magnetic modified biomass was analyzed by using cationic dyes: methylene blue and basic magenta as model dyes. Optical micrograph and x-ray diffraction analyses showed that Fe(3)O(4) particles were precipitated on the modified biomass surface. The as-prepared biosorbent could be recycled easily by using an applied magnetic field. Titration analysis showed that the total concentration of the functional groups on the magnetic PMDA modified biomass was calculated to be 0.75 mmol g(-1) by using the first derivative method. The adsorption capacities (q(m)) of the magnetic PMDA modified biomass for methylene blue and basic magenta were 609.0 and 520.9 mg g(-1), respectively, according to the Langmuir equation. Kinetics experiment showed that adsorption could be completed within 150 min for both dyes. The desorption experiment showed that the magnetic sorbent could be used repeatedly after regeneration. The as-prepared magnetic modified sorbent had a potential in the dyeing industry wastewater treatment.

Environmental conditions during external fertilization in fish have a significant effect on spermatozoan motility (MOT) and fertilization ability. Even in the same family of fish, spermatozoa might differ in sensitivity to ions present in the external medium. Elucidation of such differences within a species would help to understand spermatozoan biology and to determine external conditions that would optimize spermatozoan MOT and successful fertilization. Objectives of the current study were to determine the effects of pH and of sodium, potassium, and calcium ion concentrations in the activation solution on sea trout spermatozoan MOT. Six parameters characterizing MOT (MOT, curvilinear velocity [VCL], linearity, amplitude of lateral head displacement, beat cross frequency, and duration of MOT) in spermatozoa activated in prepared buffers were traced by computer-assisted sperm analysis. Sea trout spermatozoa were motile over a wide range of pH values, and increasing pH did influence MOT, VCL, linearity, amplitude of lateral head displacement, and MOT duration. The optimum pH for sperm MOT was established at approximately 10. Increasing K(+) ion concentration within the observed range caused a decrease in MOT and VCL. Spermatozoan movement ceased at 8 mM KCl concentrations. In Ca(2+) buffers, sperm were motile within the range of 0 to 70 mM CaCl(2) concentration; although beyond 8 mM concentration, VCL and MOT gradually declined. Spermatozoan aggregation was observed at the highest ion concentrations tested. Increasing CaCl(2) concentration affected MOT pattern from initiation to termination of spermatozoan movement in a similar manner as changes associated with increasing pH. At concentrations of CaCl(2) higher than 0.5 mM and in buffers with pH values 10 to 11, movement of spermatozoa was characterized by high initial linearity followed by its gradual reduction. In contrast to the effects of KCl and CaCl(2), increasing NaCl concentration up to 90 mM Na(+) concentration prolonged the duration of spermatozoan movement and, up to 60 mM Na(+) concentration, slightly increased sperm velocity as well. Above the concentration of 90 mM NaCl, these parameters decreased; and at 240 mM of Na(+), spermatozoa did not activate., (Copyright © 2013 Elsevier Inc. All rights reserved.)

A study on the separation of lipophilic quaternary ammonium cations in NACE coupled with contactless conductivity detection (NACE-C(4)D) is presented. The suitability of different salts dissolved in various organic solvents as running electrolytes in NACE-C(4)D was investigated. A solvent mixture of methanol/acetonitrile at a ratio of 90%:10% v/v showed the best results. Deoxycholic acid sodium salt as BGE was found to provide exceptional high stability with low baseline noise that leads to highest S/N ratios for the target analytes among all BGEs tested. Under the optimum conditions, capillaries with different internal diameters were examined and an id of 50 μm was found to give best detection sensitivity. The proposed method was validated and showed good linearity in the range from 2.5 to 200 μM, low limits of detection (0.1-0.7 μM) and acceptable reproducibility of peak area (intraday RSD 0.1-0.7%, n = 3; interday RSD 5.9-9.4%, n = 3)., (© 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

Standard procedures for the tracing of ion fluxes into roots of plants are described here, with emphasis on cations, especially potassium (K(+)). We focus in particular on the measurement of unidirectional influx by use of radiotracers and provide a brief introduction to compartmental analysis by tracer efflux (CATE).

Different schemes for simultaneous separations of both cations and anions were implemented in capillary electrophoresis employing a sequential injection analysis manifold for flexible manipulation of the background electrolyte and samples. The utilization of contactless conductivity allowed sensitive detection in narrow capillaries of 10 μm internal diameter, which in turn enabled the use of hydrodynamic pumping without significant penalty in dispersion otherwise caused by the laminar nature of the flow. This allowed to position sample plugs at a desired place along the entire length of the capillary prior to electrophoretic separation or to carry out concurrent pumping during the separation itself for optimization of resolution. Also implemented was dual single-end injection, the injection of two sample plugs from one end of the capillary, and the small size of the contactless conductivity detector allowed the concurrent use of two cells at different points along the capillary for added flexibility. Equally considered was the effect of the pH-value of the background electrolyte as this strongly influences the electroosmotic flow, which also has bearing on the protocol to be used. For dual single-end injection reproducibilities in separation time of about 1-3% were obtained and the peak areas could be reproduced to within about 3-5% (both standard deviations). The detection limits for inorganic ions were all about 1 μM., (Copyright © 2012 Elsevier B.V. All rights reserved.)

A novel and simple Schiff base composed with 9-anthraldehyde and 4-aminoantipyrine was synthesized and characterized as a fluorescent probe. In the presence of Fe(3+), the fluorescent intensity has a dramatic enhancement over other examined metal ions in aqueous solution. The method of Job's plot indicated the formation of 1:1 complex between probe and Fe(3+), and the possible binding mode of the system was also proposed. Moreover, other examined metal ions had no effect on the detection of Fe(3+)., (Copyright © 2012 Elsevier B.V. All rights reserved.)

A higher selective and sensitive probe for the detection of Fe(III) in aqueous media was made using 2,4-Diisocyanatotoluene (TDI) as a bridge to couple Fe3 O4 nanoparticles(NPs) and Rhodamine-6G hydrazide. The characterization of composite materials with Infrared spectra(IR), Thermal Gravimetric analysis(TGA) and Transmission Emission Microscopy(TEM) points to the graft of Rhodamine-6G hydrazide onto the surface of the Fe3O4. The obvious color change of the probe solution from light grey to pink upon the addition of Fe3+ demonstrated the probe could be used for "naked-eye" detection of Fe3+ in water at pH 7. The presence of 1 equivalent (10 micromol x L(-1) microm) of each of these metal ions, including Mn2+, Ni2+, Y2+, Eu3+, Ce3+, La3+, Pr3+, Cd2+, Cr3+, Sm3+, Fe2+, Cu2+ and Zn2+ ions, did not demonstrate any obvious fluorescence change of the probe water solution, which confirmed the probe was a probe with remarkable selectivity for Fe3+. And the fluorescence images of HeLa cells in physiological solutions after incubation with Fe3+ and then further incubated with the probe leading to a strong intracellular fluorescence, which suggested the probe could penetrate the HeLa cell membrane and could respond to Fe3+ in intracellular within living cells.

Four series of dicephalic cationic surfactants, considered as new antielectrostatic agents have been investigated in order to establish their toxicity and biodegradability. Among them N,N-bis[3,3'-(dimethylamine)propyl]alkylamides, N,N-bis[3,3'-(dimethylamine)propyl]alkylamide dihydrochlorides, N,N-bis[3,3'-(trimethylammonio)propyl]alkylamide dibromides and N,N-bis[3,3'-(trimethylammonio)propyl]alkylamide dimethylsulphates with different hydrophobic chain length (n-C(9)H(19) to n-C(15)H(31)) and type of counterion (chloride, bromide and methylsulfate) have been studied. The inhibitory effect against microorganisms has been examined using model gram-positive and gram-negative bacteria, and yeasts. None of the tested surfactants have shown antimicrobial activity against gram-negative bacteria (Escherichia coli, Pseudomonas putida) and yeasts (Saccharomyces cerevisiae, Rhodotorula glutinis) at a concentration below 1000 μg mL(-1), however some of them were moderately active against gram-positive bacteria (Staphylococcus aureus, Bacillus subtilis). The Microtox® test was successfully applied to measure EC(50) values of the studied dicephalic cationic surfactants. Their toxicity to Vibrio fischeri depended upon the alkanoyl chain length with the EC(50) values in a range of 2.6-980 mg L(-1). N,N-bis[3,3'-(dimethylamine)propyl]alkylamide dihydrochlorides 2a-b and N,N-bis[3,3'-(trimethylammonio)propyl]alkylamide dibromides 3a-b comprising n-decanoyl and n-dodecanoyl hydrophobic tails appeared to be the least toxic. Furthermore, the biodegradability under aerobic conditions of 2a-b, 3a-b was evaluated using OECD Method 301F. According to the obtained results 2a, 3a-3b can be considered as almost readily biodegradable and they are not expected to be persistent in the environment. Additionally, partial biodegradation was observed for 2b, indicating its possible biodegradation in wastewater treatment systems., (Copyright © 2012 Elsevier Ltd. All rights reserved.)

This study deals with the characteristics of throughfall produced by vine (Vitis vinifera L.) in one of the most common pedoclimatic conditions for grape production: a soil derived from marine sediments under a temperate Mediterranean climate, and located rather close to the seacoast. To distinguish the contribution of the plant from that of the atmospheric deposition, the throughfall was collected for more than one year under real and artificial (plastic) vines; for the same period, also the bulk precipitation was collected. The solution collected were analysed for pH, electrical conductivity, and concentration of cations and anions. For each event, the ionic fluxes of bulk precipitation and throughfall were calculated. Results indicated that the chemical composition of the bulk precipitation was strongly influenced by the proximity of the seashore and, to a lesser extent, by local anthropic activities and windblown material coming from distant areas. The chemical composition of the throughfall was affected by the same factors of bulk precipitation, but also by solubilisation of dry deposition trapped by the canopies, agronomic practices, plant, and living-on-the-leaves microorganisms. The comparison of the characteristics of the throughfall of the real with the artificial vines revealed that the vines are a source of Mg and K. During winter season, the reduction of Ca, NH(4) and PO(4) from bulk precipitation to throughfall was ascribed to the formation of biogenic minerals on the plant surface. The presence of these minerals was proved by X-ray diffraction on the powders collected during the winter season on the surface of cordons and fruiting canes. We conclude that an approach to the estimation of the nutritional potentiality of the soil that includes the contribution of the throughfall is functional to the management of the agro-ecosystem., (Copyright © 2012 Elsevier B.V. All rights reserved.)

In the current paper, a novel amphoteric straw-based adsorbent was prepared and applied to adsorb various dyes from aqueous solutions. The amphoteric adsorbent was proven effective in eliminating both cationic and anionic dyes (methylene blue and acid green 25), especially at corresponding favored pH conditions. The fundamental adsorption behavior of the adsorbent on removing various dyes was also investigated at different temperatures. The adsorption isotherms were all best-fitted by the Langmuir equation, whereas the adsorption kinetics was well-described by both the pseudo-second order model and the Elovich model. The experimental result revealed that the adsorption mechanism followed the monolayer chemical adsorption with an ion-exchange process., (Copyright © 2012 Elsevier Ltd. All rights reserved.)

This study reports the development and validation of a fast capillary electrophoresis method for cation determination in honey samples and the classification of honey by geographical origin using Principal Components Analysis (PCA). The background electrolyte (BGE) was optimized using the Peakmaster(®) software, which evaluates the tendency of the analytes to undergo electromigration dispersion and the BGE buffer capacity and conductivity. The final BGE composition was defined as 30 mmol L(-1) imidazole, 300 mmol L(-1) acetic acid and 140 mmol L(-1) Lactic acid, at pH 3,0, and the separation of K(+), Na(+), Ca(2+), Mg(2+) and Mn(2+) using Ba(2+) as the internal standard was achieved in less than 2 min. The method showed satisfactory results in terms of linearity (R(2)>0.999), the detection limits ranged from 0.27-3.17 mg L(-1) and the quantification limits ranged from 0.91-10.55 mg L(-1). Precision measurements within 0.55 and 4.64%RSD were achieved and recovery values for the analytes in the honey samples ranged from 93.6%-108.6%. Forty honey samples were analyzed to test the proposed method. These samples were dissolved in deionized water and filtered before injection. The CE-UV reliability in the cation analysis in the real sample was compared statistically with ICP-MS methodology. No significant differences were found, with a 95% confidence interval between the methodologies. The PCA showed that the cumulative variance for the first two principal components explain more than 85% of the variability of the data. The analytical data suggest a significant influence of the geographical origin on the mineral composition., (Copyright © 2012 Elsevier B.V. All rights reserved.)

The intensification of agriculture in recent decades has resulted in extremely high nitrogen inputs to ecosystems. One effect has been H(+) release through NH(4)(+) oxidation in soils, which increases rock weathering and leads to acidification processes such as base-cation leaching from the soil exchange complex. This study investigated the evolution of cation concentrations over the past 50 years in rivers from the Armorican crystalline shield (Brittany, western France). On a regional scale, acidification has resulted in increased base-cation riverine exports (Ca(2+), Mg(2+), Na(+), K(+)) correlated with the increased NO(3)(-) concentration. The estimated cation increase is 0.7 mmol(+)/L for Ca(2+) + Mg(2+) and 0.85 mmol(+)/L for total cations. According to mass balance, cation loss represents >30% of the base-cation exchange capacity of soils. Long-term acidification thus contributes to a decline in soil productivity. Estimates of the total organic nitrogen annually produced worldwide indicate that acidification may also constitute an additional carbon source in crystalline catchments if compensated by liming practices.

Cu is an essential element for plant growth, but the molecular mechanisms of its distribution and redistribution within the plants are unknown. Here, we report that Yellow stripe-like16 (YSL16) is involved in Cu distribution and redistribution in rice (Oryza sativa). Rice YSL16 was expressed in the roots, leaves, and unelongated nodes at the vegetative growth stage and highly expressed in the upper nodes at the reproductive stage. YSL16 was expressed at the phloem of nodes and vascular tissues of leaves. Knockout of this gene resulted in a higher Cu concentration in the older leaves but a lower concentration in the younger leaves at the vegetative stage. At the reproductive stage, a higher Cu concentration was found in the flag leaf and husk, but less Cu was present in the brown rice, resulting in a significant reduction in fertility in the knockout line. Isotope labeling experiments with (65)Cu showed that the mutant lost the ability to transport Cu-nicotianamine from older to younger leaves and from the flag leaf to the panicle. Rice YSL16 transported the Cu-nicotianamine complex in yeast. Taken together, our results indicate that Os-YSL16 is a Cu-nicotianamine transporter that is required for delivering Cu to the developing young tissues and seeds through phloem transport.

This paper reports the fabrication of polyester-toner (PT) electrophoresis microchips with improved analytical performance and extended lifetime. This has been achieved with a better understanding about the EOF generation and the influence of some parameters including the channel dimensions (width and depth), the injection mode, and the addition of organic solvent to the running buffer. The analytical performance of the PT devices was investigated using a capacitively coupled contactless conductivity detector and inorganic cations as model analytes. The proposed devices have exhibited EOF values of (3.4 ± 0.2) × 10(-4) cm(2) V(-1) s(-1) with good stability over 25 consecutive runs. It has been found that the EOF magnitude depends on the channel dimension, i.e. the wider the channel, the higher the EOF value. The separation efficiency for inorganic cations ranged from 13 000 to 50 000 plates/m. The LOD found for K(+) , Na(+) , and Li(+) were 4.2, 7.3, and 23 μM, respectively. In addition, the same PT device has been used by three consecutive days. Lately, due to improved analytical performance, it was carried out by the first time the detection of inorganic cations in real samples such as energetic drinks and pharmaceutical formulations., (© 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

A Hg(2+) chemodosimeter P3 derived from a perylenebisimide scaffold and thiourea fragments was systematically studied with focus on the photophysical, chemodosimetric mechanistic, as well as fluorogenic behaviors toward various metal cations for the sake of improving selectivity to Hg(2+). As demonstrated, Hg(2+) can promote a stepwise desulfurization and N-acylation of P3 with the help of an acetate anion (OAc(-)), resulting in an N-acylated urea derivative. Interestingly, OAc(-) has the effect of improving the selectivity of P3 to Hg(2+) among other metal ions; that is, in an acetone/Britton-Robinson buffer (9:1, v/v; pH 7.0) upon excitation at 540 nm, the relative fluorescence intensity is increased linearly with increasing concentration of Hg(2+) in the range of 2.5-20 μM with a detection limit of 0.6 μM, whereas the fluorescence intensity of P3 to other metal ions, including Na(+), K(+), Mg(2+), Ca(2+), Mn(2+), Fe(2+), Ni(2+), Co(2+), Zn(2+) Ag(+), Cd(2+), Pb(2+), and Cu(2+), is negligible. The fluorescent bioimaging of chemodosimeter P3 to detect Hg(2+) in living cells was also reported.

An indirect UV detection method based on capillary electrophoresis was developed to separate eleven metal cations completely, including alkali, alkaline earth and transition metal, which are related to evaluate the quality of honey. The background electrolyte contains 15 mmol/L chromophore imidazole, and acetic acid (pH = 3.7), which functioned as pH adjustor and complexing reagent. The selected cations can be completely separated within 8 min under hydrodynamic mode injection with a running voltage of 20 kV at 25°C. Limit of detection, linearity, reproducibility relative standard deviation of migration time and recoveries are in the range of 0.01-0.21 mg/L, 0.06-60.0 mg/L, 2.1-3.4% and 95.4-104.1%, respectively. The applicability of the method is shown by the analysis of honey samples, including a comparison with results of pretreatment and unpretreatment of eight samples. The results demonstrate that the developed method can conveniently be used in routine analysis of honey.

Otolith microchemistry can provide valuable information about stock structure and mixing patterns when the magnitude of environmental differences among areas is greater than the cumulative influence of any vital effects. Here, the current understanding of the underlying mechanisms governing element incorporation into the otolith is reviewed. Hard and soft acid and base (HSAB) theory is employed to explore the differences in chemical behaviours, distributions and affinities between elements. Hard acid cations (e.g. Mg(2+) , Li(+) and Ba(2+) ) tend to be less physiologically influenced and accepted more readily into the otolith crystal lattice but are relatively homogeneous in seawater. Soft acid cations (e.g. Zn(2+) and Cu(2+) ) on the other hand, exhibit more varied distributions in seawater, but are more likely to be bound to blood proteins and less available for uptake into the otolith. The factors influencing the geographical distribution of elements in the sea, and their incorporation into the otoliths of marine fishes are reviewed. Particular emphasis is placed on examining physiological processes, including gonad development, on the uptake of elements commonly used in population studies, notably Sr. Finally, case studies are presented that either directly or indirectly compare population structuring or movements inferred by otolith elemental fingerprints with the patterns indicated by additional, alternative proxies. The main obstacle currently limiting the application of otolith elemental microchemistry to infer movements of marine fishes appears to lie in the largely homogeneous distribution of those elements most reliably measured in the otolith. Evolving technologies will improve the discriminatory power of otolith chemistry by allowing measurement of spatially explicit, low level elements; however, for the time being, the combination of otolith minor and trace element fingerprints with alternative proxies and stable isotopic ratios can greatly extend the scope of migration studies. Among the otolith elements that routinely occur above instrument detection limits, Ba, Mn and Li were deemed the most likely to prove reliable geographic markers in marine species., (© 2012 The Authors. Journal of Fish Biology © 2012 The Fisheries Society of the British Isles.)

Polymyxins have been the only alternative therapeutic option for the treatment of serious infections caused by multidrug-resistant Acinetobacter baumannii or Pseudomonas aeruginosa isolates. For this reason, it is of crucial importance that susceptibility tests provide accurate results when testing these drug-pathogen combinations. In this study, the effect of cation concentration variability found on different commercial brands of Mueller-Hinton agar (MHA) for testing polymyxin B susceptibility was evaluated. The polymyxin B susceptibilities determined using Etest and disk diffusion were compared to those determined by the CLSI reference broth microdilution method. In general, the polymyxin B MIC values were higher when determined by Etest than when determined by broth microdilution against both A. baumannii and P. aeruginosa isolates. A high very major error rate (10%) was observed, as well as a trend toward lower MICs, compared to those determined by broth microdilution when the Merck MHA was tested by Etest. Poor essential agreement rates (10 to 70%) were observed for P. aeruginosa when all MHA brands were tested by Etest. Although an excellent categorical agreement rate (100%) was seen between the disk diffusion and broth microdilution methods for P. aeruginosa, larger zones of inhibition were shown obtained using the Merck MHA. The high cation concentration variability found for the MHA brands tested correlated to the low accuracy, and discrepancies in the polymyxin B MICs were determined by Etest method, particularly for P. aeruginosa isolates.

The potential for groundwater and surface water pollution by nutrients in organic residues, primarily nitrogen (N) and base cations (K+, Na+, Ca2+, Mg2+), is a consideration when applying such residues to land. In this study, we used a laboratory column leaching procedure to examine the leaching of N, K+, Na+, Ca2+ and Mg2+ in soils treated with two types of raw organic residues (poultry manure and potato residues) and one municipal waste compost, which are currently recycled on agricultural land in Iran. Each organic residue was thoroughly mixed with two different soils (sandy loam and clay) at the rate of 3%. Soil columns were leached at 4-d intervals for 92 d with distilled water, and effluents were analysed for pH, EC, nitrate (NO3(-)-N), ammonium (NH4(+)-N) K+, Na+, Ca2+ and Mg2+. The results indicated that the amounts of NO3(-)-N and NH4(+)-N leached from the poultry manure and potato residues could represent very important economic losses of N and pose an environmental threat under field conditions. The sandy loam soil amended with poultry manure lost the highest amount of NO3(-)-N (206.4 kg ha(-1)), and clay soil amended with poultry manure lost the highest amounts of NH4(+)-N (454.3 kg ha(-1)). The results showed that a treatment incorporating 3% of municipal waste compost could be used without negative effects to groundwater N concentration in clay soil. Significant amounts of K+, Na+, Ca2+, and Mg2+ were leached owing to the application of poultry manure, potato and municipal waste compost to soils. There was a positive relationship between K+, Na+, Ca2+, and Mg2+ with NO3(-)-N and NH4(+)-N leached in soils. Analysis of variance detected significant effects of amendment, soil type and time on the leaching NO3(-)-N, NH4(+)-N, K+, Na+, Ca2+ and Mg2+.

The synthesis and spectral characterization of a schiff base, 2-pyridinecarbaldehyde-p-phenylenedihydrazone (short for 2PC-PPH), were described. It was found that ferric ion (Fe(3+)) could selectively quench the fluorescence of 2PC-PPH, whereas many other metal ions, such as Mn(2+), Zn(2+), Cu(2+), K(+), Al(3+), Ca(2+), Ni(2+), Co(2+), Cr(3+) and Fe(2+), could not quench its fluorescence. Based on this, a sensitive method for ferric ion selective detection was established. Under the optimum conditions, the decreasing fluorescence intensity of 2PC-PPH is proportional to the concentration of Fe(3+) within the range of 6.0×10(-7)-1.0×10(-5) mol L(-1). The detection limit (3σ) for Fe(3+) determination is 3.6×10(-7) mol L(-1). The proposed method was successfully applied to determine iron in tea and milk powder., (Copyright © 2012 Elsevier B.V. All rights reserved.)

The metabolome is the complete set of small molecules coming from protein activity (anabolism and catabolism) in living systems. They have a broad range of chemical structures and physicochemical properties and therefore different analytical methodologies are necessary. Highly polar metabolites, such as sugars and most amino acids are not retained by conventional reversed-phase LC columns. Without sufficient retention, coelution may result in identification problems while the detection of compounds by MS at low concentrations may also be problematic due to ion suppression. In order to retain compounds based on their hydrophilicity, polar stationary phases and hydrophilic-interaction LC provide a complementary tool to reversed-phase LC for untargeted comprehensive metabolite fingerprinting. However, robustness of the methods is still limiting their applications. This review focuses on sample pretreatment, stationary phases, analytical methods and applications for polar compound analysis in biological matrices.

Two new Schiff base derivatives {2,2'-diphenyl-N,N'-bis(2-pyridylmethylene)biphenyl-4,4'-diamine} (1) and {2,2'-diphenyl-N,N'-bis(salicylidene)biphenyl-4,4'-diamine} (2) were synthesized and characterized by means of elemental analysis, (1)H NMR, FT-IR, and standard spectroscopy techniques. The molecular structure of 2 has been determined by X-ray single crystal analysis. The analyses of fluorescence properties of the compounds revealed that 1 and 2 are both poorly fluorescent and display sensitive fluorescence responses to a panel of 24 monovalent, divalent, and trivalent metal ions in CH(3)CN-DMSO (9:1, v/v). Results with imine 1 showed that Fe(3+), Cu(2+), Zn(2+), Cd(2+), Mn(2+), Zr(4+), Hg(2+), Cr(2+), Pb(2+), Sn(2+), Bi(2+), Al(3+), Ce(3+), La(3+), Sm(3+), Gd(3+), Nd(3+), Eu(3+) and Dy(3+) yields red shifts in emission and increases in intensity. And the greatest spectral changes for imine 2 include enhancements in emission intensity coupled with red shifts (Zr(4+), Sn(2+), Al(3+) and Zn(2+)) and strong quenching (Fe(3+)). The fluorescence enhancement mechanism of 1 and 2 for metal ions is based on: (i) CN isomerization; (ii) chelation-enhanced fluorescence (CHEF) effect; and (iii) excited-state intra/intermolecular proton transfer (ESPT)., (Copyright © 2012 Elsevier B.V. All rights reserved.)

This work demonstrates that the recognition of cations by molecular switches can give rise to large contrasts of the second-order nonlinear optical (NLO) properties, which can therefore be used as a powerful and multi-usage detection tool. The proof of concept is given by evidencing, by means of ab initio calculations, the ability of spiropyran/merocyanine systems to selectively detect alkali, alkaline earth, and transition-metal cations.

Rain water samples, covering 44 rain events of 2008 and 52 rain events of 2009, were collected at urban and suburban locations of Varanasi and analyzed for pH, conductivity and for metal and nutrient ions. The pH of rainwater varied between 6.3 and 7.9, with over 70% of samples having alkaline range. Volume weighed mean concentration of ions indicated Ca2+ (11.62- 41.60 microeq l(-1)) to be the most dominant species followed by SO4(2-) (4.7-25.2 microeq I(-1)), Na+ (1.60-10.25 microeq l(-1)), Mg2+ (0.22-7.21 microeq I(-1)), (NO3(-) (0.73-4.02 microeq l(-1)), K+(0.50-3.70 microeq l(-1)) and PO4(3-) (0.02-0.97 microeq l(-1)) respectively. Among the heavy metals, Cr (12.60 to 44.60 microg l(-1)), Zn (4.25 to 34.55 microg l(-1)) and Mn (10.62 to 28.40 microg l(-1)) were found to be the dominant component of rain water. The varimax rotation of PCA results extracted four major factors namely urban-industrial emission, crustal aerosols, wind transport and biomass burning accounting for 80% of the total variance. The study has relevance in establishing cause-effect relationships for terrestrial as well as for aquatic ecosystems.

Part 1 (see companion paper) of the present study discussed the application of a multimethod approach in characterizing the size of cerium oxide nanoparticles (NPs). However, other properties less routinely investigated, such as shape and morphology, structure, chemical composition, and surface properties, are likely to play an important role in determining the behavior, reactivity, and potential toxicity of these NPs. The present study describes the measurement of the aforementioned physicochemical properties of NPs (applied also to nanomaterials [NMs]) compared with micrometer particles (MPs). The authors use a wide range of techniques, including high resolution-transmission electron microscopy, scanning electron microscopy, atomic force microscopy, X-ray diffraction, X-ray energy dispersive spectroscopy, electron energy loss spectroscopy, X-ray photoelectron spectroscopy, and electrophoresis, and compare these techniques, their advantages, and their limitations, along with recommendations about how best to approach NM characterization, using an application to commercial cerium oxide NPs and MPs. Results show that both cerium oxide NPs and MPs are formed of single polyhedron or truncated polyhedron crystals. Cerium oxide NPs contain a mixture of Ce(3+) and Ce(4+) cations, whereas the MPs contain mainly Ce(4+) , which is potentially important in understanding the toxicity of cerium oxide NPs. The isoelectric point of cerium oxide NPs was approximately pH 8, which explains their propensity to aggregate in aqueous media (see companion paper)., (Copyright © 2012 SETAC.)

A new chemosensor molecule 3 based on a ferrocene-imidazophenanthrophenazine dyad effectively recognizes Hg(2+) in an aqueous environment through three different channels. Upon recognition, an anodic shift of the ferrocene-ferrocenium oxidation potential (ΔE(1/2) = 240 mV) and a progressive red shift (Δλ = 17 nm) of the low energy band in its absorption spectrum is produced. The emission spectrum of 3 in an aqueous environment, CH(3)CN-EtOH-H(2)O (65:25:10), and conducted at pH = 7.4 (20 × 10(-3) M HEPES) (Φ = 0.003), is perturbed after addition of Hg(2+) cations and an intense and structureless red shift emission band at 494 nm (Δλ = 92 nm) appeared along with an increase of the intensity of the emission band (CHEF = 77), the quantum yield (Φ = 0.054) resulted in a 18-fold increase. The combined (1)H NMR data of the complex and the theoretical calculations suggest the proposed bridging coordination mode.

A new method for the determination of five cations (sodium, ammonium, potassium, magnesium and calcium) in wines and beverages was developed and validated based on capillary ion chromatography. With a capillary ion exchange column (IonPac CS12A, 250 mm x 0.4 mm, 8 microm) and 18 mmol/L methanesulfonic acid (MSA) elution, the five cations can be well separated in 15 min. After suppression with a capillary suppressor (CCES 300), the background was much decreased, and the sensitivities of the cations were greatly improved. For the milky tea, acetonitrile was added into the sample solution to deposit the proteins. With the pretreatment of an OnGuard RP cartridge to remove hydrophobic substances in the sample, the developed method can be applied to the determination of the cations in wines and beverages. The calibration curves of peak area versus concentration gave correlation coefficients more than 0.9997 for these cations. Average recoveries were between 95.2% - 103.3%. The method is suitable for the determination of alkali metals and alkaline-earth metals in wines and beverages. The capillary ion chromatography provides analysis with less solvent consumption and better column efficiency, also possesses the advantages of high sensitivity, good selectivity and environmental friendly.

In this study, our recent work on advanced ion chromatographic methods for the simultaneous determination of inorganic ionic species such as common anions (SO4(2-), Cl(-) and NO3(-)) and cations (Na+, NH4+, K+, Mg2+, and Ca2+), nutrients (phosphate and silicate) and hydrogen ion/alkalinity are summarized first. Then, the applications using these methods for monitoring environmental water quality are also presented. For the determination of common anions and cations with nutrients, the separation was successfully performed by a polymethacrylate-based weakly acidic cation-exchange column of TSKgel Super IC-A/C (Tosoh, 150 mm x 6.0 mm i. d.) and a mixture solution of 100 mmol/L ascorbic acid and 4 mmol/L 18-crown-6 as acidic eluent with dual detection of conductivity and spectrophotometry. For the determination of hydrogen ion/alkalinity, the separation was conducted by TSKgel ODS-100Z column (Tosoh, 150 mm x 4.5 mm i. d.) modified with lithium dodecylsulfate and an eluent of 40 mmol/L LiCl/0.1 mmol/L lithium dodecylsulfate/0.05 mmol/L H2SO4 with conductivity detector. The differences of ion concentration between untreated and treated wastewater showed the variation of ionic species during biological treatment process in a sewage treatment plant. Occurrence and distribution of water-quality conditions were related to the bioavailability and human activity in watershed. From these results, our advanced ion chromatographic methods have contributed significantly for water quality monitoring of environmental waters.

Green (vegetated) roofs are emerging as practical strategies to improve the environmental quality of cities. However, the impact of green roofs on the storm water quality remains a topic of concern to city planners and environmental policy makers. This study investigated whether green roofs act as a source or a sink of various metals (Na, K, Ca, Mg, Al, Fe, Cu, Cd, Pb, Zn, Mn, Cr, Ni, Li and Co), inorganic anions (NO3-, NO2-, PO4(3-), SO4(2-), Cl-, F- and Br-) and cation (NH4+). A series of green roof assemblies were constructed. Four different real rain events and several artificial rain events were considered for the study. Results showed that concentrations of most of the chemical components in runoff were highest during the beginning of rain events and subsided in the subsequent rain events. Some of the important components present in the runoff include Na, K, Ca, Mg, Li, Fe, Al, Cu, NO3-, PO4(3-) and SO4(2-). However, the concentration of these chemical components in the roof runoff strongly depends on the nature of substrates used in the green roof and the volume of rain. Based on the USEPA standards for freshwater quality, we conclude that the green roof used in this study is reasonably effective except that the runoff contains significant amounts of NO3- and PO4(3-)., (Copyright © 2011 Elsevier Ltd. All rights reserved.)

This work reports an ion chromatographic (IC) method for the quantitative determination of inorganic cations (Na(+), K(+), Mg(2+) and Ca(2+)) in biodiesel samples that were synthesized from different vegetable oils and fat. The proposed method uses water extraction, heating and ultrasound. The limits of detection (LOD) for each ion, in milligrams of the analyte per kilogram of biodiesel (mgkg(-1)), were respectively: 0.11 (Na(+)); 0.42 (K(+)); 0.23 (Ca(2+)); and 0.36 (Mg(2+)). The accuracy of the method was studied through recovery tests. For comparison, two samples were also analyzed using an Inductively Coupled Plasma Optical Emission Spectrometry (ICP-OES) procedure. The paired Student t test and the Snedecor F test showed that both methods offer equivalent results in terms of accuracy and precision. The operational simplicity, accuracy and precision of the proposed method suggest that it can be a good alternative for the determination of inorganic cations in biodiesel samples., (Copyright © 2012 Elsevier B.V. All rights reserved.)

Capillary ion electrophoresis-capacitively coupled contactless conductivity detection (CIE-C4D) with a polyvinyl alcohol chemically coated capillary (PVA capillary) was used to analyze inorganic cations (Na(+), K(+), NH(4)(+), Mg(2+), and Ca(2+)) commonly found in human saliva. The PVA capillary, which was made by our laboratory, minimized electro-osmotic flow in the wide pH range of the background electrolyte (BGE), and the PVA layer adsorbed to capillary wall did not affect the conductimetric background level. In this study, we determined an optimized BGE of 30 mM lactic acid/histidine plus 3 mM 18-crown-6 for the CIE-C4D system using the PVA capillary, which could simultaneously improve the separation of Mg(2+) and Ca(2+) from Na(+) and that of K(+) from NH(4)(+). This system obtained highly reproducible separation of cations in human saliva samples within 8 min at 20 kV without deprotonation. The quantifiability of cations in human saliva samples on the CIE-C4D system was demonstrated through identification by ion chromatography with satisfactory results.

A re-survey of acid-sensitive lakes in Ireland (initial survey 1997) was carried out during spring 2007 (n = 60). Since 1997, atmospheric emissions of sulfur dioxide and deposition of non-marine sulfate (SO(4) (2-)) in Ireland have decreased by ~63 and 36%, respectively. Comparison of water chemistry between surveys showed significant decreases in the concentration of SO(4) (2-), non-marine SO(4) (2-), and non-marine base cations. In concert, alkalinity increased significantly; however, no change was observed in surface water pH and total aluminum. High inter-annual variability in sea salt inputs and increasing (albeit non-significant) dissolved organic carbon may have influenced the response of pH and total aluminum (as ~70% is organic aluminum). Despite their location on the western periphery of Europe, and dominant influence from Atlantic air masses, the repeat survey suggests that the chemistry of small Irish lakes has shown a significant response to reductions in air pollution driven primarily by the implementation of the Gothenburg Protocol under the UNECE Convention on Long-Range Transboundary Air Pollution.

Estimation of base cation supply from mineral weathering (BC(w)) is useful for watershed research and management. Existing regional approaches for estimating BC(w) require generalized assumptions and availability of stream chemistry data. We developed an approach for estimating BC(w) using regionally specific empirical relationships. The dynamic model MAGIC was used to calibrate BC(w) in 92 watersheds distributed across three ecoregions. Empirical relationships between MAGIC-simulated BC(w) and watershed characteristics were developed to provide the basis for regionalization of BC(w) throughout the entire study region. BC(w) estimates extracted from MAGIC calibrations compared reasonably well with BC(w) estimated by regression based on landscape characteristics. Approximately one-third of the study region was predicted to exhibit BC(w) rates less than 100 meq/m(2)/yr. Estimates were especially low for some locations within national park and wilderness areas. The regional BC(w) results are discussed in the context of critical loads (CLs) of acidic deposition for aquatic ecosystem protection., (Copyright © 2011 Elsevier Ltd. All rights reserved.)

A highly selective and sensitive ratiometric fluorescent chemosensor for Ag(+) in aqueous solution was developed, in a linear range of 0.6 × 10(-7) to 50 × 10(-7) mol L(-1), based on a A-Ag(+)-A binding mode with a heptamethine cyanine motif containing one adenine moiety., (This journal is © The Royal Society of Chemistry 2012)

The development of surface-attached sensors for cationic and anionic guests is of intense current research interest. In addition to the environmental flexibility, robustness and reusability of such devices, surface-confined sensors typically exhibit an amplified response to target analytes owing to preorganization of the receptor. Whereas redox-active cations may be sensed by studying the cyclic voltammetry of host-guest systems containing ion-selective receptors attached to an appropriate electrode, redox-inactive ionic species require the use of electrochemical impedance spectroscopy, with appropriately functionalized electrodes and redox probes. Alternatively, receptors may be constructed that incorporate an electrochemical or optical reporter group within their structure to provide a macroscopic response to the presence of an ionic guest. This critical review seeks to present an up-to-date, although necessarily selective, account of the progress in the field, and provides insights into possible future developments, including the utilization of receptor-nanoparticle conjugates and mechanically interlocked receptors.

The quality of drinking water (tap, ground, and spring) in Toyama Prefecture, Japan was assessed by studying quality indicators including major ions, total carbon, and trace metal levels. The physicochemical properties of the water tested were different depending on the water source. Major ion concentrations (Ca(2+), K(+), Si(4+), Mg(2+), Na(+), SO(4)(2-), HCO(3)(-), NO(3)(-), and Cl(-)) were determined by ion chromatography, and the results were used to generate Stiff diagrams in order to visually identify different water masses. Major ion concentrations were higher in ground water than in spring and tap water. The relationship between alkaline metals (Na(+) and K(+)), alkaline-earth metals (Ca(2+) and Mg(2+)), and HCO(3)(-) showed little difference between deep and shallow ground water. Toyama ground, spring, and tap water were all the same type of water mass, called Ca-HCO(3). The calculated total dissolved solid values were below 300 mg/L for all water sources and met World Health Organization (WHO) water quality guidelines. Trace levels of As, Cd, Cr, Co, Cu, Fe, Pb, Mn, Mo, Ni, V, Zn, Sr, and Hg were detected in ground, spring, and tap water sources using inductively coupled plasma atomic emission spectrometry, and their levels were below WHO and Japanese water quality standard limits. Volatile organic carbon compounds were quantified by headspace gas chromatography-mass spectrometry, and the measured concentrations met WHO and Japanese water quality guidelines. Total trihalomethanes (THMs) were the major contaminant detected in all natural drinking water sources, but the concentration was highest in tap water (37.27 ± 0.05 μg/L). Notably, THMs concentrations reached up to 1.1 ± 0.05 μg/L in deep ground water. The proposed model gives an accurate description of the organic, inorganic, and trace heavy metal indicators studied here and may be used in natural clean water quality management., (© Springer Science+Business Media B.V. 2011)

One of the ultimate goals of ion chromatography is to determine both anions and cations found in samples with a single chromatographic run. In the present article, recent progress in ion-exclusion/ion-exchange chromatography for the simultaneous determinations of inorganic anions and cations are reviewed. Firstly, the principle and the control for the simultaneous separation and detection of analyte ions using ion-exclusion/cation-exchange chromatography with a weakly acidic cation-exchange column are outlined. Then, advanced chromatographic techniques in terms of analytical time, selectively and sensitivity are summarized. As a related method, ion-exclusion/anion-exchange chromatography with an anion-exchange column could be used for the simultaneous determination of inorganic nitrogen species, such as ammonium, nitrite and nitrate ions. Their usefulness and applications to water-quality monitoring and related techniques are also described.

This article aims to find a reliable procedure by which to remove Cd(2+) from water and store it safely. The proposed procedure includes Cd(2+) uptake by a zeolitic tuff, a natural cation exchanger, followed by stabilization of the contaminated solid in a hardened lime matrix. Several tuff-lime pastes were examined and their safety tested by cation leaching and mechanical strength measurement. It was demonstrated that a very cheap mixture, containing only 10% lime, is able to safely retain the harmful cation and may be disposed of in a segregated landfill.

The review presents fluorescence spectroscopic studies on the capacities of newly synthesized polypropyleneamine and polyamidoamine fluorescent dendrimers to detect biologically important metal ions. It has been shown that those fluorescent dendrimers whose periphery comprises 1,8-napthalimide fragments are highly sensitive to metal ions which are of great importance to the living organisms.