Assessment of persistent organic pollutants in soil and sediments from an urbanized flood plain area

Polycyclic aromatic hydrocarbons (PAHs), organochlorine pesticides (OCPs) and phenolic compounds (PCs) are persistent organic compounds. Contamination of these potentially toxic organic pollutants in soils and sediments is most studied environmental compartments. In recent past, studies were carried out on PAHs, OCPs and PCs in various soils and sediments in India. But, this is the first study on these pollutants in soils and sediments from an urbanized river flood plain area in Delhi, India. During 2018, a total of fifty-four samples including twenty-seven each of soil and sediment were collected and analyzed for thirteen priority PAHs, four OCPs and six PCs. The detected concentration of ∑PAHs, ∑OCPs and ∑PCs in soils ranged between 473 and 1132, 13 and 41, and 639 and 2112 µg/kg, respectively, while their concentrations in sediments ranged between 1685 and 4010, 4.2 and 47, and 553 and 20,983 µg/kg, respectively. PAHs with 4-aromatic rings were the dominant compounds, accounting for 51 and 76% of total PAHs in soils and sediments, respectively. The contribution of seven carcinogen PAHs (7CPAHs) in soils and sediments accounted for 43% and 61%, respectively, to ∑PAHs. Among OCPs, p, p’-DDT was the dominant compound in soils, while α-HCH was found to be dominated in sediments. The concentrations of ∑CPs (chlorophenols) were dominated over ∑NPs (nitrophenols) in both the matrices. Various diagnostic tools were applied for the identification of their possible sources in soil and sediments. The observed concentrations of PAHs, OCPs and PCs were more or less comparable with the recently reports from various locations around the world including India. Soil quality guidelines and consensus-based sediment quality guidelines were applied for the assessment of ecotoxicological health effect.

     

Organochlorines in urban soils from Central India: probabilistic health hazard and risk implications to human population

This study presents distribution of organochlorines (OCs) including HCH, DDT and PCBs in urban soils, and their environmental and human health risk. Forty-eight soil samples were extracted using ultrasonication, cleaned with modified silica gel chromatography and analyzed by GC-ECD. The observed concentrations of ∑HCH, ∑DDT and ∑PCBs in soils ranged between?<?0.01–2.54, 1.30–27.41 and?<?0.01–62.8 µg kg^?1, respectively, which were lower than the recommended soil quality guidelines. Human health risk was estimated following recommended guidelines. Lifetime average daily dose (LADD), non-cancer risk or hazard quotient (HQ) and incremental lifetime cancer risk (ILCR) for humans due to individual and total OCs were estimated and presented. Estimated LADD were lower than acceptable daily intake and reference dose. Human health risk estimates were lower than safe limit of non-cancer risk (HQ?<?1.0) and the acceptable distribution range of ILCR (10^?6–10^?4). Therefore, this study concluded that present levels of OCs (HCH, DDT and PCBs) in studied soils were low, and subsequently posed low health risk to human population in the study area.     

Sediment-associated trace and major metals in the headwaters of a tropical reservoir

Bed sediment samples of the two headwaters of a tropical reservoir in Southwestern Nigeria were analysed for some metal concentrations using ICP-OES for a period of one year. Sediment samples were collected bi-monthly from both the lower and upper reaches of the streams from May 2013 to March 2014. Sediment samples were microwave-digested and analysed using ICP-OES. Concentrations of metals were higher in the lower reach than in the upper reach, and wet season concentrations were higher than in the dry season with the exception of Fe and Mn. The annual mean metal concentrations were as follows: Fe (121.72?±?6.82?µg/g); Mn (9.34?±?2.57?µg/g); Na (6.20?±?2.29?µg/g); K (0.65?±?0.57?µg/g); Mg (8.07?±?1.36?µg/g); Ca (13.92?±?2.85?µg/g); Ba (0.17?±?0.17?µg/g); Al (106.54?±?5.55?µg/g); and Se (0.6?±?0.19?µg/g). These values were lower in comparison with the baseline concentrations of elements on the earth’s crust. Contamination assessment of all the metals investigated in this study showed that metals in the bed sediments of the two headstreams had not reached pollution status with the exception of Se.     

Distribution of mercury in the sediments of some freshwater bodies in Ethiopia

Sediment samples were collected from Tinishu Akaki River (TAR), Lake Awassa, and Lake Ziway, Ethiopia for determination of mercury. The air-dried samples were analyzed for mercury with a differential atomic absorption spectrometer after thermal evaporation of bound mercury converting it to its atomic form. Certified reference materials (CRMs) of sediments and soils were used to validate the method. The recovery of mercury from CRMs and sediments was in the range of 95–100%. The limit of detection for the determination of mercury was 50?ng?kg^?1. The concentration of total mercury in the sediments varied from 3.9 to 110?µg?kg^?1 for TAR, 14 to 67?µg?kg^?1 for Lake Awassa, and 17 to 110?µg?kg^?1 for Lake Ziway. It was found that the total mercury concentrations in all samples were below the United States Environmental Protection Agency guideline of 200?µg?kg^?1.     

The accumulation levels of heavy metals (Ni,Cr, Sr, & Ag) in marine algae from southwest coast of India

In the context of use of marine algae as biological indicators of heavy metal pollution in coastal waters, six species of marine algae collected from the southwest coast of India were analysed for the levels of heavy metals (Ni, Cr, Sr, and Ag). Interspecies and interclass variations were determined on a spatial and temporal scale. The metal contents varied in the ranges, Ni: 0.20–21.06?µg?g^?1 (mean?=?10.13?µg?g^?1), Cr: non-detectable level (ND)–37.18?µg?g^?1 (mean?=?13.86?µg?g^?1), Sr: 2.19–103.90?µg?g^?1 (mean =?29.40?µg?g^?1), and Ag: ND–6.39?µg?g^?1 (mean?=?1.80?µg?g^?1). Ni and Cr contents were of similar magnitude to those reported for algae from polluted areas.     

Concentrations of polycyclic aromatic hydrocarbons in soils of a mangrove forest affected by forest fire

Surface soils affected by forest fires from Igbanko mangrove forest in Nigeria were analyzed for 16 EPA priority polycyclic aromatic hydrocarbons (PAHs) using gas chromatography–mass spectrometry (GC–MS). The total PAHs concentrations in the soils ranged from 63 to 188?µg?kg^?1 dry weight (average: 108?µg?kg^?1). The three predominant PAHs in the soils were naphthalene (Na), fluoranthene (Flu), and benzo(b)fluoranthene (BbF). Compared to the control sample (19?µg?kg^?1), elevated PAHs concentrations were observed in the soils, an indication of some level of PAHs contamination. PAHs source diagnostic ratios of Flu/(Flu?+?Pyr) and Ant/(Ant?+?Phe) indicated that the PAHs have a pyrogenic origin which may have resulted from combustion of grass, wood, or coal. An assessment based on Canadian soil quality guidelines indicated that the studied locations do not pose any serious adverse risk on human health.     

A novel extraction method for analysing available sulfamethoxazole in soil

A novel extraction method was established to determine the water-extractable (available) content of sulfamethoxazole (SMX) in soil. The SMX imprinted polymers (MIPs) were synthesised and the performance was evaluated by Fourier transform infrared spectroscopy, scanning electron microscopy and binding experiments. Results showed that the MIPs exhibited good selectivity for SMX, so the MIPs were applied as a sorbent. SMX in soil was extracted by water, sorbed from the extract to MIPs and analysed with a high performance liquid chromatography (HPLC) after its desorption from MIPs. Meanwhile, the classic organic solvent extraction was employed to measure the total SMX content in soil. Results showed that when SMX level in spiked soils varying from 1.0–500?μg?kg^?1, the observed recoveries of available SMX contents ranged from 63.27?±?3.11% to 82.11?±?2.77% (n?=?3), while the total SMX varied between 89.59?±?1.65% and 97.64?±?3.92% (n?=?3). The detection limit of the developed method for SMX in soils was 0.05?μg?kg^?1. Available SMX contents in five field soil samples ranged from 0.13 to 4.14?μg?kg^?1, which were only 0.35–25.40% of the respective total SMX contents. Results from this study manifest the importance of the extents of SMX immobilisation with different soils for assessing SMX's ecological and human health risks.     

Toxicokinetics,metabolism, and microsomal studies of chlorpropham in rats

A study on the toxicokinetic behavior, metabolism of chlorpropham, and its effect on cytochrome P₄₅₀ from liver microsomes was carried out in albino rats after a single and consecutive oral administration at 500?mg?kg^?1 body weight for 10 and 20 days. Chlorpropham was detected in the blood at 0.08?h (11.43?±?1.72?µg?mL^?1) reaching a maximum concentration at 2?h (30.90?±?2.55?µg?mL^?1) and a minimum at 48?h (1.95?±?0.20?µg?mL^?1) after a single oral administration of 500?mg?kg^?1. The absorption rate constant (K _a) was 0.66?±?0.48?h^?1. The Vd _area (18.01?±?2.78?L?kg^?1) and t _1/2 β (12.23?±?1.96?h) values suggested a wide distribution and long persistence of the compound in the body, respectively. The higher Cl_R (0.82?±?0.00?L?kg^?1?h^?1) compared to Cl_H (0.18?±?0.02?L?kg^?1?h^?1) value indicated that a major portion of chlorpropham was excreted through the urine (30%) compared to the faeces (2.81%). Chlorpropham residue was detected in all tissues of rat at 0.25?h while its metabolite, meta-chloroaniline was detected in liver, kidney, heart, lung, and spleen tissue at 0.25?h. Meta-chloroaniline was not detected in skeletal muscle, brain, fat, and stomach tissue at any time of the observation period. Maximum concentrations of chlorpropham and meta-chloroaniline were detected at 2?h (except in the spleen), and minimum concentrations of chlorpropham at 24 (heart, lung, spleen, skeletal muscle, and stomach) and 48?h (liver, kidney, brain, and fat tissue) respectively; and meta-chloroaniline at 24?h (except heart and spleen). The tissue half-life of chlorpropham in rat varied from 3.80 to 11.60?h. Repeated oral administration of chlorpropham at 500?mg?kg^?1 for 10 and 20 days caused an induction of the liver microsomal pellet of rat.     

Mercury concentrations in the surface sediments of the intertidal area along the west coast of Peninsular Malaysia

Total mercury (Hg) levels in the intertidal surface sediments along the west coast of Peninsular Malaysia were analysed by using heat vaporization method. Total Hg levels in these sediments ranged from 3.00 to 201?µg?kg^?1 dry weight with a mean concentration of 60.0?µg?kg^?1 dry weight. More than 90% of the samples studied have the total Hg concentrations less than 150?µg?kg^?1 dry weight. Compare with the regional data and sediment quality guidelines, the Hg contamination in the intertidal area along the west coast of Peninsular Malaysia was not serious, except for a few sites that might have received anthropogenic Hg in the samples collected between 1999 and 2000. It is suggested that a similar study of heavy metals in the sediments of the west coast of Peninsular Malaysia be conducted regularly.     

Concentrations of lead in cosmetics commonly used in South Africa

In this study, we present evidence of lead in lip liner, oil absorbent powder, mascara, concealer, lipsticks, lip gloss, and foundation. The samples were analyzed for lead by flame atomic absorption spectrometry. The levels of lead in concealer, mascara, lip liner, and oil absorbent powder were found to be 7.4?±?1.3?µg?g^?1, 15.8?±?0.2?µg?g^?1, 29.0?±?9.2?µg?g^?1, and 17.3?±?2.9?µg?g^?1, respectively. The levels of lead in lipsticks, lip gloss, and foundation ranged from not detected to 73.1?±?5.2?µg?g^?1, 4.7 to 11.7?±?2.8?µg?g^?1, and 7.8 to 32.9?±?1.4?µg?g^?1, respectively. Thus, in the majority of samples, the concentrations of lead are higher than the USFDA maximum permissible concentration of 0.10?µg?g^?1 in candy and cosmetics. In lipsticks alone, only 25% of 40 samples were found to meet the requirement. Therefore, continuous use of cosmetic products in which lead concentration exceeds the maximum permissible level may pose a health hazard for the female population of South Africa in the long run.     

Persistence of carbaryl and its risk assessment through consumption of treated grapes

The average initial deposits of carbaryl were observed to be 1.4 and 3.1?mg?kg^?1, respectively, following four applications of the insecticide at 4.95 and 9.9?kg active ingredient per hectare. Residues of carbaryl dissipated below its limit of quantification of 50?µg?kg^?1 after 7 and 10 days at single and double the application dosage, respectively. The half-life values (t _1/2) of carbaryl were worked out to be 1.3 and 0.7 days, respectively, at single and double dosages. The acceptable daily intake (ADI) for carbaryl has been fixed at 8?µg?kg^?1 body weight per day. Keeping in view the residues of carbaryl observed one day after the last application, a child of 10?kg and an adult of 60?kg will have an intake of 77 and 154?µg carbaryl after consumption of 100 and 200?g grapes, in comparison to its ADI of 80 and 480?µg; thus, no health risk is to be expected. Therefore, a waiting period of 1 day has been suggested for the safe consumption of carbaryl-treated grapes to avoid any health hazards.     

Aliphatic and polycyclic aromatic hydrocarbon contamination in surface sediment of the Chitrapuzha River,South West India

Distribution (seasonal and spatial) of aliphatic and polycyclic aromatic hydrocarbons (PAHs) in surface sediments of the Chitrapuzha River, Cochin, India, was investigated using gas chromatography. Significantly high concentrations prevailed during the pre-monsoon season with the industrial zones of the river appearing to be hot spots with particularly elevated levels of the hydrocarbons. AHCs ranged between 7754 and 41,173?ng/g with an average of 25,256?ng/g, while total PAHs varied from 5046 to 33,087?ng/g. n-Alkane indices and PAH diagnostic ratios point to petroleum contamination in the sediments. The significance of PAHs in the sediments was explored using universally accepted interpretation tools. Observed levels of PAHs in sediments of Chitrapuzha are likely to cause adverse effects on biota.     

Speciation analysis of butyltin compounds in sediments of the Theoule harbour (France) by GC/AES

Over the last years, great progress in the research on speciation of butyltins has been made. Many coupling techniques have been successfully developed, with better applications to sediments samples in the environment. Sediments were collected from 1999 to 2000 to elucidate butyltin pollution in Theoule harbour. Most of the analysed samples showed evidence of butyltin compounds. The results show that the concentration of Tributyltin (TBT) was in the range 20–200?µg/kg in March 1999, 20–340?µg/kg in June 1999, 180–1280?µg/kg in July 2000, and 55–820?µg/kg in October 2000. A comparison of the MBT, DBT, and TBT results show that in 1999 the concentrations were in the order TBT?DBT?>?MBT, with some exceptions. The patterns observed in many sediment cores show a great disparity of organotin input concentration among the cores collected during one month and also during two different months, and from one season to the other. This paper provides information on the use of the acetic acid leaching system in the determination of butyltin. The method is applied to evaluate the occurrence of these species in sediments from the Theoule harbour, between 1999 and 2000. In this study, a GC/AES was applied, complemented with acetic acid leaching and monitored using two certified reference materials: PACS-2 reference sediment and BCR 462 (Report EUR 18406 EN, 1998).     

Arsenic in freshwater ecosystems of the Bengal delta: status,sources and seasonal variability

The study aimed to examine the contamination status of arsenic (As) in excavated small water bodies, commonly known as ponds – the integral part of daily life in the arsenic-affected rural areas of West Bengal, India in comparison to the unaffected areas. The ponds of the contaminated area had higher levels of As: water 2–174 µg L^?1 (mean 31 ± 2 µg L^?1) and sediment 1.3–37.3 mg kg^?1 (mean 10.3 ± 0.4 mg kg^?1), than those from the unaffected area: water 1–8 µg L^?1 (mean 4 ± 0 µg L^?1) and sediment 1.4–5.3 mg kg^?1 (mean 3.0 ± 0.1 mg kg^?1). A moderate positive correlation was observed between the water and sediment arsenic content of the ponds of the arsenic-affected region (r = 0.688, n = 277, p < 0.0001). Contaminated ground water, either as direct input or through agricultural washings, was found to be the major contributor of arsenic pollution to these ecosystems. Seasonal variations were not prominent. This study emphasized the beneficial role of using the studied ecosystems over the highly contaminated ground water for various livelihood activities in the Gangetic delta region.     

Liver and renal histopathology of North Atlantic long-finned pilot whales (Globicephala melas) contaminated with heavy metals and organochlorine compounds

Long-finned pilot whales (Globicephala melas) from the Faroe Islands are known to be heavily polluted with contaminants, such as mercury (Hg) and organochlorine compounds (OC). This is postulated to exert adverse health effects on whales as well as the human population who rely on its meat and blubber as food sources. It was therefore decided to conduct a screening pilot study to determine contaminant concentrations and histopathology of liver and renal tissues in a total of 14 specimens from this subpopulation. In blubber, the mean ∑OC concentration was 31,887 ng g^?1 lw (range: 18,170–47,425 ng g^?1 lw) of which ∑PCB concentration was 23,416 ng g^?1 lw (range: 13,947–34,543 ng g^?1 lw; n = 3). In liver, mean Hg concentration was 138 µg^?1 ww (range: 54–351 µg g^?1 ww; n = 7) and mean cadmium (Cd) concentration 15 µg g^?1 ww (range: 7–31 µg g^?1 ww; n = 7). In the kidney, the mean Cd concentration was 36 µg g^?1 ww (range: 23–47 µg g^?1 ww; n = 7). Of the liver Hg concentrations, two were at the suggested toxic threshold levels of 60 µg g^?1 ww and five were 2–6-fold above. Liver selenium (Se) : Hg was on average 1.11 (range: 0.97–1.41; n = 7) indicating that Se was in excess, which decreased the risk of acute Hg poisoning. Histopathological examinations showed high prevalence (>35%) of renal glomerular arteriosclerosis, glomerular capillary dilatation, dilatation and hyalinization of Bowman's space/capsule and tubular hyaline casts. In liver tissue, high prevalence was found for portal cell infiltrates, lipid granulomas, hepatocytic lipid accumulation, bile duct proliferation, lipid-filled Ito cells, and focal necrosis. In a single juvenile male, 4 of 8 renal and 3 of 7 liver lesions were present. Cadmium concentrations increased significantly in the presence of glomerular arteriosclerosis and a similar trend was found for tubular hyaline casts. Based on these findings, as well as the nature of the lesions, data indicate that the histopathological changes were a result of age and that contaminants are likely to be the co-factors in the development in at least three renal and four liver lesions.     

Fish as an indicator of aquatic environment: Multielemental neutron activation analysis of nutrient and pollutant elements in fish from Indian coastal areas

Fish is the main food in coastal areas and its analysis for toxic metals has been used as an indicator of the pollution status of the aquatic environment. Several different fish species from the three Indian coasts, Visakhapatnam in the east, Mumbai in the west and Mangalore in the south west and also inland freshwater fish from Nagpur in the central region for comparison were analyzed for up to 20 elements (As, Au, Ba, Br, Cl, Co, Cr, Cu, Fe, Hg, K, Mn, Na, P, Rb, Sb, Sc, Se, Sr, Zn) by instrumental neutron activation analysis (INAA). Dried fish samples in powdered form were irradiated with thermal neutrons in a nuclear reactor followed by high resolution gamma ray spectrometry at different intervals. Several Reference Materials (RMs) of biological origin were analyzed for quality assurance and data validation. Elemental contents in different fish species vary in a wide range depending on the species, its size, location, and aquatic environment. Fish from Mangalore showed highest mean contents of Cr (14.8?±?29.9?µg?g^?1), Cu (1005?±?643?µg?g^?1) and Sb (849?±?888?ng?g^?1) whereas those from Mumbai exhibited highest Hg (2066?±?2146?ng?g^?1) and P (20.3?±?4.63?µg?g^?1) but lowest Cu (6.30?±?3.10?µg?g^?1) contents. Fish from all the regions showed significant amounts of nutrient elements such as Na, K, P, Mn, Fe, Se and Zn as well as some pollutant elements (Br, Cr, Sb, Hg). No regularity in variation of elemental contents with the size was observed. Prawn (Panaeus latisulcatus), a popular fish species from four different regions showed wide variation in elemental contents of Cr, Mn, Fe, Zn, Se, P including toxic pollutants, Sb and Hg. An attempt has been made to calculate daily dietary intake (DDI) for some nutrient elements from Indian fish. Elemental data for Cr, Cu, Fe, Hg, Se, and Zn have been compared with those from other fish exporting countries.     

Trace element concentration levels in three bird species in Hormod Protected Area,Larestan, Iran

The objective of the present study was to investigate the levels of Cd, Pb, Co, and Cu, in A. chukar, A. griseogularis, and Columba livia, in order to (1) examine the age- and gender-related variation in trace metal accumulation and (2) to determine the significance between metal concentrations in the kidney, liver, and pectoral muscle. Mean concentrations of Cd and Pb in the kidney of A. chukar, A. griseogularis, and C. livia were 3.7, 4.1, and 3.9?µg/g and 15.9, 13.6, and 15.5?µg/g, respectively. In the liver, they were 4.8, 4.3, and 3.9?µg/g and 21.4, 21.3, and 21.1?µg/g, and in the pectoral muscle, 2.3, 2.3, and 2.2?µg/g and 7.1, 7.1, and 7.8?µg/g, respectively. Metal concentrations in three bird species were decreased in the sequence of liver?>?kidney?>?pectoral muscle. Trace metal concentrations in the three species were higher in females than in males. The mean concentrations of Cd in the kidney and liver were higher than the background levels, as well as Pb concentrations in the liver were higher than the toxic level.     

Neurotoxicity and oxidative stress induced by permethrin in gills of the freshwater mussel Unio ravoisieri

Pyrethroids are contaminants found in the aquatic environment, and their toxicological effects on aquatic organisms have received extensive attention. However, the impact on freshwater bivalve of exposure to these chemicals is still largely unknown. Freshwater mussels Unio ravoisieri were exposed to two nominal permethrin (PM) concentrations C1?=?50?µg/L and C2?=?100?µg/L during 7 days. The measured concentrations of PM using gas chromatography (GC/ECD) in the treated aquariums were, respectively, 28.7–62.3?µg/L. Catalase (CAT), Glutathione-S-transferase (GST), and Acetylcholinesterase (AChE) activities, Glutatione (GSH) and Malondialdehyde (MDA) levels were determined in gills of U. ravoisieri. Significant increase in CAT activity by the lowest concentration and decrease by highest concentration were observed. Additionally, GST activity was increased in a concentration-dependent manner. However, statistically significant decrease in GSH levels (about 39%) was observed only at high concentration of this compound (100?µg/L). PM generated an increase in MDA levels reaching the highest value at the high concentration. AChE activity of mussel ranging from 51% inhibition at lowest concentration 50?µg/L to 89% inhibition at highest concentration 100?µg/L. The results indicated that oxidative stress and cell damage might be one of the main mechanisms of PM toxicity to freshwater mussels.     

Polychlorinated-dibenzo-p-dioxins, -dibenzofurans and -dioxin-like polychlorinated biphenyls in aquatic organisms from lake Kasumigaura,Japan

Polychlorinated-dibenzo-p-dioxins (PCDDs), -dibenzofurans (PCDFs) and -dioxin-like polychlorinated biphenyls (DLPCBs) were determined in aquatic wildlife of Kasumigaura Lake (KUL), Japan from 1978 to 2001. Two plankton species elucidated several fold greater concentrations (2400–7800) than small tiger fish (310–6500), shrimp (160–1100), and three large fish namely, black bass (120–240), carp (94–120) and mullet (54) on pg/g fat. PCDD homologues were predominant accumulants with >68–<95% contribution and remaining was shared by PCDFs. Accumulation, non-ortho DLPCBs in plankton (3500–9200), shrimp (1600–8600) and small fish (2000–8800) and large fish (1300–3900) on ng/g fat basis were several orders magnitude greater than PCDD/DFs. The mono-ortho DLPCBs in large fish species were 23?000–83?000?ng/g fat and which it is accounted 94.3–95.9% the total dioxin-like PCBs accumulation. Temporal trends of PCDDs, PCDFs, non-ortho PCBs and TEQ in shrimp and small tiger fish were varied. The mullet had minimum toxic equivalency “TEQ” (14?pg?TEQ/g) followed by plankton Neomysis intermedia (25?pg?TEQ/g), small tiger fish (mean: 33, ranges 14–66?pg?TEQ/g), plankton Cyclopus vicinus (34?pg?TEQ/g), carp (mean: 35, ranges 32–38?pg?TEQ/g), shrimp (mean: 38, ranges 11–68?pg?TEQ/g) and black bass (mean: 59, ranges 38–79?pg?TEQ/g) on fat basis. In all the samples, PCDD was predominant TEQ contributor followed by PCDFs and DLPCBs. The contribution of mono-ortho DLPCBs to the total TEQ was 0.52–0.92 in large fish.     

Arsenic speciation in rice consumed in south-western Nigeria,and estimation of dietary intake of arsenic species through rice consumption

This study determined concentrations and speciation of arsenic (As) in rice samples obtained from the cities of Akure, Ore, Ondo and Ikare in Ondo State, south-western Nigeria. The estimated dietary intake of As from rice consumption for total As and the identified As species were compared with the As benchmark dose lower confidence limit. Analyses of rice from the four cities identified three As species: inorganic As, monomethylarsonic, acid and dimethylarsinic acid. Concentrations of total As and the As species differed significantly across the sampling locations (by a factor of 2.5 for total As). Mean levels (±S.D.) were 58.8 ± 0.7 µg/kg total As, 47.0 ± 0.6 µg/kg inorganic As, 0.33 ± 0.03 µg/kg monomethylarsonic acid, and 11.5 ± 0.1 µg/kg dimethylarsinic acid. The estimated mean dietary intakes were 4.1 µg/d total As, 3.3 µg/d inorganic As, 0.02 µg/d monomethylarsonic acid, and 0.8 µg/d dimethylarsinic acid. These values are below the benchmark dose lower confidence limit and comparable to, or lower than, those reported for other countries. Thus, consumption of rice cultivated in south-western Nigeria does not appear to have inherent As-associated health risks.