The role of fingernail selenium in the association between arsenic, lead and mercury and child development in rural Vietnam: a cross-sectional analysis.

As, Pb and Hg are common environmental contaminants in low- and middle-income countries. We investigated the association between child toxicant exposure and growth and development and determined if this association was mitigated by Se concentration. Toxicant concentrations in fingernail samples, anthropometry and Bayley's Scales of Infant Development, 3rd edition domains were assessed in 36-month-old children whose mothers had been part of a randomised controlled trial in rural Vietnam. Multivariable regression analyses were performed to estimate the effect of toxicant exposure on clinical outcomes with adjustments for potential confounders and interaction with fingernail Se concentration. We analysed 658 children who had data for at least one physical or developmental outcome, and at least one toxicant measurement, and each of the covariates. Fingernail As concentration was negatively associated with language (estimate per 10 % increase in As: -0·19, 95 % CI: (-0·32, -0·05)). Pb was negatively associated with cognition (estimate per 10 % increase in Pb: -0·08 (-0·15, -0·02)), language (estimate per 10 % increase in Pb: -0·18 (-0·28, -0·10)) and motor skills (estimate per 10 % increase in Pb: -0·12 (-0·24, 0·00)). Hg was negatively associated with cognition (estimate per 10 % increase in Hg: -0·48, (-0·72, -0·23)) and language (estimate per 10 % increase in Hg -0·51, (-0·88, -0·13)) when Se concentration was set at zero in the model. As Se concentration increased, the negative associations between Hg and both cognition and language scores were attenuated. There was no association between toxicant concentration and growth. As, Pb and Hg concentrations in fingernails of 3-year-old children were associated with lower child development scores. The negative association between Hg and neurological development was reduced in magnitude with increasing Se concentration. Se status should be considered when assessing heavy metal toxicants in children and their impact on neurodevelopmental outcomes.

Localization of nickel in the hyperaccumulator plant Breynia cernua (Poir.) Mull.Arg. discovered in the nickeliferous laterites of Zambales, the Philippines.

A newly discovered nickel (Ni) hyperaccumulator plant, Breynia cernua (Phyllanthaceae) from the nickeliferous laterites of Acoje, Zambales, has elevated Ni concentrations. Its computed bioaccumulation factor is 1.7 and the translocation factor is 4.6. Leaf tissues which contain the highest Ni concentrations were analyzed using optical microscopy and Scanning Electron Microscopy with Energy-Dispersive X-ray (SEM/EDX). The results indicated that most of the Ni are stored in the epidermal cells of the leaves, followed by the mesophyll cells then the vascular bundles. The accumulation of Ni found in the subcellular locations, probably in the vacuoles, may prevent phytotoxicity that could affect the normal function of other cellular structures. A possible resistance mechanism through strain avoidance towards Ni accumulation makes B. cernua capable of tolerating elevated Ni concentrations in its tissues. The tolerance of B. cernua to Ni phytotoxicity suggests possible applications of this hyperaccumulator plant in phytoextraction technology.

Copper uptake by Pteris melanocaulon Fée from a Copper-Gold mine in Surigao del Norte, Philippines.

The ability of some plants to take up metal contaminants in the soil has been of increasing interest as an environmental approach to pollution clean-up. This study aimed to assess the ability of Pteris melanocaulon for copper(Cu) uptake by determining the Cu levels in the fern vis-à-vis surrounding soil and the location of Cu accumulation within its biomass. It also aimed to add information to existing literature as P. melanocaulon are found to be less documented compared to other fern metal accumulators, such as P. vittata. The P. melanocaulon found in the Suyoc Pit of a Copper-Gold mine in Placer, Surigao del Norte, Philippines exhibited a high Bioaccumulation Factor(BF) of 4.04 and a low Translocation Factor(TF) of 0.01, suggesting more Cu accumulation in the roots (4590.22 ± 385.66 µg g(-1) Cu). Noteworthy was the Cu concentration in the rhizome which was also high (3539.44 ± 1696.35 µg g(-1) Cu). SEM/EDX analyses of the Cu content in the roots indicated high elemental %Cu in the xylem (6.95%) than in the cortex (2.68%). The high Cu content in the roots and rhizomes and the localization of Cu in the xylem manifested a potential utilization of the fern as a metallophyte for rhizofiltration and phytostabilization.

Localization of mercury and gold in cassava (Manihot esculenta Crantz).

The potential of cassava (Manihot esculenta Crantz.) for simultaneous Hg and Au phytoextraction was explored by investigating Hg and Au localization in cassava roots through Micro-Proton Induced X-Ray Emission, High-Resolution Transmission Electron Microscopy (HR-TEM) and X-Ray Diffractometry (XRD). The effect of Hg and Au in the cyanogenic glucoside linamarin distribution was also investigated using Matrix Assisted Laser Desorption Ionization Fourier Transform Ion Cyclotron Resonance Mass Spectrometry (MALDI-FT-ICR-MS) imaging. Hg was located mainly in the root vascular bundle of plants grown in 50 or 100 µmol L-1 Hg solutions. Au was localized in the epidermis and cortex or in the epidermis and endodermis for 50 and 100 µmol L-1 Au solutions, respectively. For 50 µmol L-1 solutions of both Hg and Au, the two metals were co-localized in the epidermis. When the Hg concentrations were increased to 100 µmol L-1, Au was still localized to a considerable extent in the epidermis while Hg was located in all root parts. HR-TEM and XRD revealed that Au nanoparticles were formed in cassava roots. MALDI-FT-ICR-MS imaging showed linamarin distribution in the roots of control and plants and metal-exposed plants thus suggesting that linamarin might be involved in Hg and Au uptake and distribution.

PHYTOREMEDIATION OF INORGANICS: REALISM AND SYNERGIES.

There are very few practical demonstrations of the phytoextraction of metals and metalloids from soils and sediments beyond small-scale and short-term trials. The two approaches used have been based on using 1) hyperaccumulator species, such as Thlaspi caerulescens (Pb, Zn, Cd, Ni), Alyssum spp. (Ni, Co), and Pteris vittata (As) or 2) fast-growing plants, such as Salix and Populus spp. that accumulate above-average concentrations of only a smaller number of the more mobile trace elements (Cd, Zn, B). Until we have advanced much more along the pathway of genetic isolation and transfer of hyperaccumulator traits into productive plants, there is a high risk in marketing either approach as a technology or stand-alone solution to clean up contaminated land. There are particular uncertainties over the longer-term effectiveness of phytoextraction and associated environmental issues. Marginally contaminated agricultural soils provide the most likely land use where phytoextraction can be used as a polishing technology. An alternative and more useful practical approach in many situations currently would be to give more attention to crops selected for phytoexclusion: selecting crops that do not translocate high concentrations of metals to edible parts. Soils of brownfield, urban, and industrial areas provide a large-scale opportunity to use phytoremediation, but the focus here should be on the more realistic possibilities of risk-managed phytostabilization and monitored natural attenuation. We argue that the wider practical applications of phytoremediation are too often overlooked. There is huge scope for cross-cutting other environmental agenda, with synergies that involve the recovery and provision of services from degraded landscapes and contaminated soils. An additional focus on biomass energy, improved biodiversity, watershed management, soil protection, carbon sequestration, and improved soil health is required for the justification and advancement of phytotechnologies.

Phytostabilisation of arsenical gold mine tailings using four Eucalyptus species: growth, arsenic uptake and availability after five years.

Arsenic (As) contamination is a worldwide problem. Where arsenic is highly concentrated and confined within a limited area, such as in many mine tailings facilities, phytostabilisation is an attractive technology for long-term remediation. Important characteristics of a plant to be useful for phytostabilisation include As tolerance and low levels of As accumulation, as well as the ability to limit As availability. Performance needs to be monitored over the long term to ensure an ongoing vegetation community, though this is rarely done. In this study, the suitability of four Eucalyptus species (E. cladocalyx, E. melliodora, E. polybractea, E. viridis) for the phytostabilisation of arsenical, sulphidic gold mine tailings was assessed after five years. All four species accumulated low As concentrations, the highest being recorded in mature leaves, ranging from 0.29 to 5.14 microg g(-1) As. E. polybractea had significantly higher foliar As than the other three species but there was also great variation within the species. Between 5-10 times lower concentrations were recorded in stem samples and no As was detected in young leaf tips. There was also significant variation in the growth of trees upon the site. Eucalyptus cladocalyx grew significantly taller than other species although greater variation was detected within the species than between. The variation in tree heights was not correlated with As concentrations in either stems or leaves. Arsenic availability was determined to depths of 2.2 m and found to be low when compared to total As in the tailings. Importantly, no effect of trees on As availability or soil pH was detected. We conclude that E. cladocalyx, in particular is an ideal candidate for the long-term phytostabilisation of As-contaminated land and mine tailings. The variation detected in both As accumulation and growth is also promising for the selection of desirable traits.

Volatile chemical emissions from fragranced baby products.

Fragranced consumer products have been associated with adverse effects on human health. Babies are exposed to a variety of fragranced consumer products, which can emit numerous volatile organic compounds (VOCs), some considered potentially hazardous. However, fragranced baby products are exempt from disclosure of all ingredients. Consequently, parents and the public have little information on product emissions. This study investigates VOCs emitted from a range of fragranced baby products, including baby hair shampoos, body washes, lotions, creams, ointments, oils, hair sprays, and fragrance. The products were analysed using gas chromatography/mass spectrometry (GC/MS) headspace analysis. Of the 42 baby products tested, 21 products made claims of green, organic, or all-natural. Results of the analysis found 684 VOCs emitted collectively from the 42 products, representing 228 different VOCs. Of these 684 VOCs, 207 are classified as potentially hazardous under federal regulations, representing 43 different VOCs. The most common VOCs emitted were limonene, acetaldehyde, ethanol, alpha-pinene, linalool, beta-myrcene, acetone, and beta-pinene. A comparison between ingredients emitted and ingredients listed reveals that only 5% of the 684 VOCs, including 12% of 207 potentially hazardous VOCs, were listed on the product label, safety data sheet, or website. More than 95% of both green and regular products emitted one or more potentially hazardous VOCs. Further, emissions of the most prevalent VOCs from green, organic, or all-natural products were not significantly different from regular products. Results from this study can help improve public awareness about emissions from baby products, with the aim to reduce pollutant exposure and potential adverse effects on babies.

Performance measurement via sap flow monitoring of three eucalyptus species for mine site and dryland salinity phytoremediation.

Monitoring of trees with reliable technology is essential in phytoremediation. Sap flow instrumentation on three Eucalyptus species at a mine site in western Victoria, Australia, was used to determine which species is best suited to meet the goals of a phytoremediation project. Specifically, the aim of the monitoring was to determine which species could better tolerate the hypersaline soil, potentially lower saline ground water, and cope with expected hotter and drier weather given climate change scenarios. Over a summer period, average daily water use of E. cladocalyx was approximately six times greater than E. melliodora and four times greater than E. polybractea. During a three day heat wave event, E. cladocalyx was found to have a higher tolerance to extreme temperature. The optimal VPD/temperature for tree transpiration was 2.6 kPa/26.2 °C for E. cladocalyx, 2.1 kPa/23.9 °C for E. melliodora, and 2.0 kPa/23.2 °C for E. polybractea. Through sap flow monitoring, it was determined that E. cladocalyx could better tolerate saline soils, hotter and drier weather, and had greater potential to lower saline ground water.

Succulent species differ substantially in their tolerance and phytoextraction potential when grown in the presence of Cd, Cr, Cu, Mn, Ni, Pb, and Zn.

Plants for the phytoextraction of heavy metals should have the ability to accumulate high concentrations of such metals and exhibit multiple tolerance traits to cope with adverse conditions such as coexistence of multiple heavy metals, high salinity, and drought which are the characteristics of many contaminated soils. This study compared 14 succulent species for their phytoextraction potential of Cd, Cr, Cu, Mn, Ni, Pb, and Zn. There were species variations in metal tolerance and accumulation. Among the 14 succulent species, an Australian native halophyte Carpobrotus rossii exhibited the highest relative growth rate (20.6-26.6 mg plant(-1) day(-1)) and highest tolerance index (78-93%), whilst Sedum "Autumn Joy" had the lowest relative growth rate (8.3-13.6 mg plant(-1) day(-1)), and Crassula multicava showed the lowest tolerance indices (<50%). Carpobrotus rossii and Crassula helmsii showed higher potential for phytoextraction of these heavy metals than other species. These findings suggest that Carpobrotus rossii is a promising candidate for phytoextraction of multiple heavy metals, and the aquatic or semiterrestrial Crassula helmsii is suitable for phytoextraction of Cd and Zn from polluted waters or wetlands.

Rinorea niccolifera (Violaceae), a new, nickel-hyperaccumulating species from Luzon Island, Philippines.

A new, nickel-hyperaccumulating species of Rinorea (Violaceae), Rinorea niccolifera Fernando, from Luzon Island, Philippines, is described and illustrated. This species is most similar to the widespread Rinorea bengalensis by its fasciculate inflorescences and smooth subglobose fruits with 3 seeds, but it differs by its glabrous ovary with shorter style (5 mm long), the summit of the staminal tube sinuate to entire and the outer surface smooth, generally smaller leaves (3-8 cm long × 2-3 cm wide), and smaller fruits (0.6-0.8 cm diameter). Rinorea niccolifera accumulates to >18,000 µg g(-1) of nickel in its leaf tissues and is thus regarded as a Ni hyperaccumulator.

Australian native plant species Carpobrotus rossii (Haw.) Schwantes shows the potential of cadmium phytoremediation.

Many polluted sites are typically characterized by contamination with multiple heavy metals, drought, salinity, and nutrient deficiencies. Here, an Australian native succulent halophytic plant species, Carpobrotus rossii (Haw.) Schwantes (Aizoaceae) was investigated to assess its tolerance and phytoextraction potential of Cd, Zn, and the combination of Cd and Zn, when plants were grown in soils spiked with various concentrations of Cd (20-320 mg kg(-1) Cd), Zn (150-2,400 mg kg(-1) Zn) or Cd + Zn (20 + 150, 40 + 300, 80 + 600 mg kg(-1)). The concentration of Cd in plant parts followed the order of roots > stems > leaves, resulting in Cd translocation factor (TF, concentration ratio of shoots to roots) less than one. In contrast, the concentration of Zn was in order of leaves > stems > roots, with a Zn TF greater than one. However, the amount of Cd and Zn were distributed more in leaves than in stems or roots, which was attributed to higher biomass of leaves than stems or roots. The critical value that causes 10% shoot biomass reduction was 115 µg g(-1) for Cd and 1,300 µg g(-1) for Zn. The shoot Cd uptake per plant increased with increasing Cd addition while shoot Zn uptake peaked at 600 mg kg(-1) Zn addition. The combined addition of Cd and Zn reduced biomass production more than Cd or Zn alone and significantly increased Cd concentration, but did not affect Zn concentration in plant parts. The results suggest that C. rossii is able to hyperaccumulate Cd and can be a promising candidate for phytoextraction of Cd from polluted soils.

Study of the spatial distribution of mercury in roots of vetiver grass (Chrysopogon zizanioides) by micro-pixe spectrometry.

Localization of Hg in root tissues of vetivergrass (Chrysopogon zizanioides) was investigated by micro-Proton Induced X-ray Emission (PIXE) spectrometry to gain a better understanding of Hg uptake and its translocation to the aerial plant parts. Tillers of C. zizanioides were grown in a hydroponic culture for 3 weeks under controlled conditions and then exposed to Hg for 10 days with or without the addition of the chelators (NH(4))(2)S(2)O(3) or KI. These treatments were used to study the effects of these chelators on localization of Hg in the root tissues to allow better understanding of Hg uptake during its assisted-phytoextraction. Qualitative elemental micro-PIXE analysis revealed that Hg was mainly localized in the root epidermis and exodermis, tissues containing suberin in all Hg treatments. Hg at trace levels was localized in the vascular bundle when plants were treated with a mercury solution only. However, higher Hg concentrations were found when the solution also contained (NH(4))(2)S(2)O(3) or KI. This finding is consistent with the observed increase in Hg translocation to the aerial parts of the plants in the case of chemically induced Hg phytoextraction.

Cd hyperaccumulative characteristics of Australia ecotype Solanum nigrum L. and its implication in screening hyperaccumulator.

A pot culture experiment was used to determine the differences in uptake characteristics of a cadmium hyperaccumulator Solanum nigrum L. discovered in China, an ecotype from Melbourne, Australia and a non-hyperaccumulator Solanum melogena Australian ecotype was not significantly different to the China ecotype. In particular, Cd concentration in leaves and shoots of S. nigrum collected from Australia were 166.0 and 146.3 mg kg(-1) respectively when 20 mg kg(-1) Cd spiked, and were not significantly different to the ecotype imported from China which had 109.8 and 85.3 mg kg(-1) respectively, in the stems and leaves. In contrast, the tolerance of the eggplant to Cd was significantly less than the two S. nigrum ecotypes. Although some morphological properties of S. nigrum collected from Australia were different from that of the plants collected from China, Cd hyperaccumulator characteristics of two ecotypes were similar. The results suggested that the tolerance and uptake of Cd may be a constitutive trait of this species.

Chemical characterisation and speciation of organic selenium in cultivated selenium-enriched Agaricus bisporus.

The selenium concentration in Agaricus bisporus cultivated in growth compost irrigated with sodium selenite solution increased by 28- and 43-fold compared to the control mushroom irrigated solely with water. Selenium contents of mushroom proteins increased from 13.8 to 60.1 and 14.1 to 137 µgSe/g in caps and stalks from control and selenised mushrooms, respectively. Selenocystine (SeCys; detected as [SeCys]2 dimer), selenomethionine (SeMet), and methyl-selenocysteine (MeSeCys) were separated, identified and quantified by liquid chromatography-electrospray ionisation-mass spectrometry from water solubilised and acetone precipitated proteins, and significant increases were observed for the selenised mushrooms. The maximum selenoamino acids concentration in caps and stalks of control/selenised mushrooms was 4.16/9.65 µg/g dried weight (DW) for SeCys, 0.08/0.58 µg/g DW for SeMet, and 0.031/0.10 µg/g DW for MeSeCys, respectively. The most notable result was the much higher levels of SeCys accumulated by A. bisporus compared to SeMet and MeSeCys, for both control and selenised A. bisporus.

Elemental and metabolite profiling of nickel hyperaccumulators from New Caledonia.

Leaf material from nine Ni hyperaccumulating species was collected in New Caledonia: Homalium kanaliense (Vieill.) Briq., Casearia silvana Schltr, Geissois hirsuta Brongn. & Gris, Hybanthus austrocaledonicus Seem, Psychotria douarrei (G. Beauvis.) Däniker, Pycnandra acuminata (Pierre ex Baill.) Swenson & Munzinger (syn Sebertia acuminata Pierre ex Baill.), Geissois pruinosa Brongn. & Gris, Homalium deplanchei (Viell) Warb. and Geissois bradfordii (H.C. Hopkins). The elemental concentration was determined by inductively-coupled plasma optical emission spectrometry (ICP-OES) and from these results it was found that the species contained Ni concentrations from to 250-28,000 mg/kg dry mass. Gas chromatography mass spectrometry (GC-MS)-based metabolite profiling was then used to analyse leaves of each species. The aim of this study was to target Ni-binding ligands through correlation analysis of the metabolite levels and leaf Ni concentration. Approximately 258 compounds were detected in each sample. As has been observed before, a correlation was found between the citric acid and Ni concentrations in the leaves for all species collected. However, the strongest Ni accumulator, P. douarrei, has been found to contain particularly high concentrations of malonic acid, suggesting an additional storage mechanism for Ni. A size exclusion chromatography separation protocol for the separation of Ni-complexes in P. acuminata sap was also applied to aqueous leaf extracts of each species. A number of metabolites were identified in complexes with Ni including Ni-malonate from P. douarrei. Furthermore, the levels for some metabolites were found to correlate with the leaf Ni concentration. These data show that Ni ions can be bound by a range of small molecules in Ni hyperaccumulation in plants.

Chelate-assisted phytoextraction of mercury in biosolids.

Mercury contaminated stockpiles of biosolids (8.4 mg kg⁻¹ Hg) from Melbourne Water's Western Treatment Plant (MW-WTP) were investigated to evaluate the possibility of their Hg chelate-assisted phytoextraction. The effects of ammonium thiosulphate (NH4)2S2O3, cysteine (Cys), nitrilotriacetic acid (NTA), and potassium iodide (KI) were studied to mobilize Hg and to increase its uptake in plant shoots. Three plant species were selected for this study, one herbaceous and two grasses: Atriplex codonocarpa, Austrodanthonia caespitosa and Vetiveria zizanioides. KI proved to be the best candidate for Hg phytostabilization in biosolids because it facilitated the concentration of this metal mainly in roots. (NH4)2S2O3 was shown to be the most effective chelating agent among those tested for Hg phytoextraction as it allowed the highest translocation of Hg into the above-ground tissues of the selected plant species. The phytoextraction conditions using A. caespitosa as the best performing plant species were optimized at an (NH4)2S2O3 concentration of 27 mmol kg⁻¹ and contact time with biosolids of seven day. Monitoring of the Hg concentration in biosolids and in leachate water during a 9-day treatment revealed that the biosolids Hg concentration decreased significantly after the first day of treatment and then it decreased only slightly with time reaching a value of 5.6 mg kg⁻¹ Hg at the end of the 9-day period. From the corresponding results obtained for the leachate water, it was suggested that a relatively large fraction of Hg (0.7 mg kg⁻¹ Hg) was promptly mobilized and consequently the plants were able to take up the metal and translocate it into shoots.

Sonochemical oxidation of arsenic(III) to arsenic(V) using potassium peroxydisulfate as an oxidizing agent.

The sonochemical oxidation of As(III) in the presence of peroxydisulfate ion (PDS) has been investigated. Sulfate anion radicals and OH radicals produced during acoustic cavitation readily oxidized As(III) to As(V) in an aqueous environment. The rate of oxidation of As(III) was remarkably high ( approximately 10 times) with respect to the concentration of PDS. The As(III) oxidation was found to be independent of the initial pH of the solution in the range 3-8. It was relatively low at pH above 8, however, this could be circumvented by increasing the concentration of PDS. The presence of oxygen in solution played a significant role in the rate of oxidation of As(III). Around 40% oxidation of As(III) was observed in the absence of oxygen compared to 80% oxidation in the presence of dissolved oxygen (10mg/L) over a sonication time of 5 min. The addition of humic acid (HA) retarded the oxidation rate of As(III), but the effect could be offset by using larger amounts of PDS. The effects of ultrasound intensity, and frequency on the rate of the oxidation of As(III) were also studied. The rate of the oxidation of As(III) was not significantly dependent on the acoustic power applied, for the concentrations of As(III) used in this study. At an ultrasound frequency of 211 kHz, the rate of oxidation of As(III) was lower than that observed at 20 kHz. It is concluded that the sonochemical treatment of As(III) solutions in the presence of PDS is a simple and viable technique for the oxidation of As(III) to As(V).

Phytotoxicity of biosolids and screening of selected plant species with potential for mercury phytoextraction.

Mercury contaminated stockpiles of biosolids (3.5-8.4 mg kg(-1) Hg) from Melbourne Water's Western Treatment Plant (MW-WTP) were investigated to evaluate the possibility for their phytoremediation. Nine plant species (Atriplex codonocarpa, Atriplex semibaccata, Austrodanthonia caespitosa, Brassica juncea, Brassica napus, Gypsophila paniculata, Sorghum bicolor, Themeda triandra and Trifolium subterraneum) were screened for phytoextraction potential in Hg-contaminated biosolids from MW-WTP. In addition, the same plant species were germinated and grown in two other substrates (i.e. potting mix and potting mix spiked with mercury(II)). Growth measurements and the mercury uptake for all three substrates were compared. Some plant species grown in potting mix spiked with mercury(II) grew more vigorously than in the other two substrates and showed higher levels of sulphur in their tissues. These results suggested that the mercury stress activated defence mechanisms and it was hypothesised that this was the likely reason for the enhanced production of sulphur compounds in the plant species studied which stimulated their growth. Some species did not grow in biosolids because of the combined effect of high mercury toxicity and high salt content. Atriplex conodocarpa and Australodanthonia caespitose proved to be the most suitable candidates for mercury phytoextraction because of their ability to translocate mercury from roots to the above-ground tissues.

Simple and efficient sonochemical method for the oxidation of arsenic(III) to arsenic(V).

A simple and efficient sonochemical method has been developed for the oxidation of acutely toxic As(III) to the less toxic As(V). The OH radicals produced during acoustic cavitation readily oxidize As(III) to As(V) in an aqueous environment The effects of various operational parameters of ultrasonication, such as power density and pulse mode, on the oxidation of As(III) were studied. Pulsed sonication showed a profound effect on the oxidation of As(III) to As(V) in comparison to the continuous mode of operation, that consequently reduced the reaction time and energy requirement for the process. Increasing acoustic amplitude led to an enhanced rate of oxidation of As(III). In the presence of As(III), the production of H2O2 was significantly reduced compared to that observed during the sonication of water alone, which suggests that OH radicals were involved in the oxidation process. The oxidation of As(III) was independent of the initial pH of the solution in the range 3 to 10.6. Continuous sparging of nitrogen through the reaction solution noticeably reduced the oxidation rate of As(III), indicating thatdissolved oxygen is involved in the oxidation process to a certain extent. It is concluded thatthe sonochemical treatment process is a simple and possibly cost-effective technique for the oxidation of As(III) to As(V) without assistance of any external chemicals or catalysts.