Human health risk assessment of arsenic in groundwater aquifers of Lahore,Pakistan

The present study was conducted to estimate As concentration in groundwater and resulting human health risk in terms of chronic daily intake, hazard quotient (HQ), hazard index (HI), and carcinogenic risk (CR) both for oral and dermal exposure to As. Groundwater samples (n = 100) were collected from ten different towns of Lahore District (Pakistan). Arsenic concentration ranged from 2 to 111 µg L^?1 in groundwater samples of the study area, which was significantly greater than the safe limit of As (10 µg L^?1) in drinking water set by the World Health Organization. Health risk assessment of As showed that HQ (0.1–11) for oral exposure and HI (0.1–11) values also exceeded the typical toxic risk index value of 1. 9.75 × E-05–4.59 × E-03 and 5.89 × E-07–2.77 × E-05 for oral and dermal As exposure, respectively. Both CR and cancer index (CIs) values were higher than United States Environmental Protection Agency limit (10^?6), suggesting that people are at high risk of As-induced carcinogenicity from oral and dermal exposure to As in drinking water. It was concluded that As contamination of groundwater causes carcinogenic and noncarcinogenic health effects to the people; therefore, urgent management and remedial actions are required to protect people from As poisoning.     

Health Risk Assessment of Chemical Mixtures Exposure to Residents in the Lake Taihu Region,China

This study assessed the mixture health risk for the residents of China's Lake Taihu region posed by a Persistent Organic Pollutants (POPs) mixture of dichloro-diphenyl-trichloroethane (DDT) and hexachlorocyclohexane (HCH). Multiple-pathway exposure models were used for exposure assessment in order to estimate the DDT and HCH exposure dose. The DDT and HCH PBPK models were developed and used for consequence assessment in order to analyze the pollutant distribution and accumulation process in human tissues. The tissue dose hazard index (HI) was used to estimate the mixture health risk. The results showed that the total exposure doses for male residents and female residents were 4.01 × 10^{? 4}～ 7.67 × 10^{? 3} mg/kg/day and 3.73 × 10^{? 4}～ 6.75 × 10^{? 3} mg/kg/day for DDT, respectively, and 3.78 × 10^{? 4}～ 5.14 × 10^{? 3} mg/kg/day and 3.53 × 10^{? 4}～ 4.66 × 10^{? 3} mg/kg/day for HCH, respectively. The maximum tissue concentrations in fat for male and female residents reached 110.51 mg/l and 97.21 mg/l for DDT, respectively, and 189.66 mg/l and 171.72 mg/l for HCH, respectively. The tissue dose hazard indexes for male and female residents were 0.1472 ～ 2.4990 and 0.1377 ～ 2.2230, respectively, and the probabilities of the risk exceeding the acceptable risk (HI = 1) for male and female were 24.60% and 16.51%, respectively.     

Environmental and Human Health Risk Assessment of Benzo(a)pyrene Levels in Agricultural Soils from the National Capital Region,Delhi, India

ABSTRACT

Exposure to benzo(a)pyrene (B(a)P) for health risk was studied in soils from the Delhi region, India. The mean and median concentrations of benzo(a)pyrene were 0.031 and 0.029 (±0.002) mg/kg, respectively. The lifetime average daily dose (LADD) for adults and children was 1.7 × 10^?8 mg kg^?1 d^?1 and 7.5 × 10^?8 mg kg^?1 d^?1, respectively, with incremental life time cancer risk (ILCR) of 1.2 × 10^?7 and 5.5 × 10^?7, respectively. The Index of Additive Cancer Risk (IACR) was 0.084. Our screening-level risk assessment shows that the observed ILCR and IACR values are much lower than the guideline values of 10^?6 ? 10^?4 (ILCR) and <1 (IACR), respectively, and therefore the measured B(a)P levels in soil may not portend environmental and human health risks.     

A quantitative risk ranking model to evaluate emerging organic contaminants in biosolid amended land and potential transport to drinking water

A quantitative risk ranking model was developed for human exposure to emerging contaminants (EC) following treated municipal sewage sludge (“biosolids”) application to Irish agricultural land. The model encompasses the predicted environmental concentration (PEC) in soil, surface runoff, groundwater, and subsequent drinking water ingestion by humans. Human exposure and subsequent risk was estimated for 16 organic contaminants using a Monte Carlo simulation approach. Nonylphenols ranked the highest across three environmental compartments: concentration in soil (PEC_soil), runoff (PEC_runoff), and groundwater (PEC_groundwater), which had mean values of 5.69 mg/kg, 1.15 × 10^?2 µg/l, and 2.22 × 10^?1 µg/l, respectively. Human health risk was estimated using the LC₅₀ (chemical intake toxicity ratio, (RR)) as a toxicity endpoint combined with PEC_runoff and PEC_groundwater. NP ranked highest for LC₅₀ combined with PEC_runoff and PEC_groundwater (mean RR values 1.10 × 10^?4 and 2.40 × 10^?3, respectively). The model highlighted triclocarban and triclosan as ECs requiring further investigation. A sensitivity analysis revealed that soil sorption coefficient and soil organic carbon were the most important parameters that affected model variance (correlation coefficient –0.89 and –0.30, respectively), highlighting the significance of contaminant and soil properties in influencing risk assessments. This model can help to prioritize emerging contaminants of concern requiring vigilance in environmental compartments.     

Monitoring of arsenic in drinking water of high schools and assessment of carcinogenic health risk in Multan,Pakistan

Abstract

This study was performed to measure arsenic (As) contents in groundwater/drinking water of high schools and its effects on human health. Chronic daily intake, hazardous quotient (HQ), carcinogenic risk (CR), hazardous index (HI), and carcinogenic indices (CI) for oral and dermal exposure to arsenic were calculated. Samples were taken from high schools in four tehsils of Multan. As contents ranged from 3.25 to 184?µg/l and 99% samples exceeded World Health Organization safe limit (10?µg/l). HQ for Multan city (1.70) and for Multan Saddar (1.38) exceeded USEPA permissible toxic risk value (1.0). CR in four tehsils for oral (0.0001–0.0003) and dermal exposure (0.0000049–0.000011) exceeded USEPA limit (10^?6). HI for tehsil Multan city (1.75) and Multan Saddar (1.42) exceeded the limit (1.0). CI for four tehsils ranged from 0.00022 to 0.0008 exceeding USEPA limit (10^?6) indicating high chronic and carcinogenic health risk to exposed population. Results indicated that groundwater of district Multan is not fit for human consumption due to excessive arsenic contamination. It invites attention of water supplying agency and educational authorities to take steps for provision of arsenic free safe drinking water to students and local area peoples.     

Human health risk assessment of trace elements in shallow groundwater of the Linhuan coal-mining district,Northern Anhui Province,China

Enrichment of trace elements in groundwater poses considerable risks to human health. The concentrations of seven trace elements (Cr, Mn, Ni, Cu, Zn, Cd, and Pb) in 34 samples of shallow groundwater from the study area were estimated. We assessed the concentrations of the trace elements and health risks with statistical analysis and the US Environment Protection Agency (USEPA) model. The results showed that the mean concentrations of trace elements decreased as follows: Mn > Zn > Ni > Cr > Cu > Cd > Pb. Apart from Mn at one sampling point, the concentrations of all trace elements were below the guideline values of the World Health Organization for drinking water. Correlation and cluster analysis indicated that the trace elements fell into groups, with Ni and Cu in one group, and Mn, Zn, and Cd in another, which suggested that the trace elements grouped together had similar sources. The total non-carcinogenic risk values ranged from 8.52 × 10^?4 to 1.27 × 10^?1. The total carcinogenic risk caused by Cr and Cd averaged 1.62 × 10^?6, which exceeded the acceptable level of 1 × 10^?6 recommended by the USEPA. The carcinogenic risk of Cr accounted for 75.93% of R_total.     

Environmental Contaminants in the Botanical Dietary Supplement Ginseng and Potential Human Risk

Botanical dietary supplements have a long history of use in Europe and Asia, but the use of these products is becoming increasing popular in the United States. Because these products are classified as dietary supplements, the U.S. Food and Drug Administration does not routinely monitor them for environmental contaminants. Ginseng served as a model botanical dietary supplement and was purchased from suppliers in the United States, Europe, and Asia. Samples were analyzed for metals (e.g., cadmium, nickel) and chlorinated pesticides (e.g., PCNB, DDT, and metabolites). Flame and furnace atomic absorption spectrophotometry were utilized for analysis of metals, while gas chromatography (GC) and GC-mass spectrophotometry were utilized for analysis of chlorinated pesticides. Because no formalized guidelines exist to determine risk of botanical dietary supplements, U.S. Environmental Protection Agency guidelines for protection of human health were used. Metals and chlorinated organics were found in Ginseng samples, but the concentrations posed no noncarcinogenic hazard; however, a 1000?mg/d dose for 350?d/yr resulted in 1 × 10^?6 carcinogenic risk in 19% of the Ginseng samples analyzed. At a lower usage rate (42?d/yr), no samples exceeded 1 × 10^?6 risk. Chlorinated organics, such as aldrin and heptachlor epoxide, accounted for the carcinogenic risk (1 X 10-6) in the Ginseng samples.     

Risk Assessment for Natural Uranium in Subsurface Water of Punjab State,India

Traces of uranium were measured by laser fluorimeter in 235 subsurface water samples collected from four districts of Punjab state in India. The concentration of U in water samples ranged between <2–644 μg/L with a mean value of 73.1 μg/L. The radiological risk was observed to be in the range of 5.55 × 10^?6–1.78 × 10^?3 with a mean value of 2.03 × 10^?4, which is around 22% more than the maximum acceptable level (l.67 × 10^?4) as per guidelines of India's Atomic Energy Regulatory Board. The mean of chemical toxicity risk, expressed as life time average daily dose (LADD) was worked out to be 5.56 μg/kg/day with a range of 0.15–48 μg/kg/day by considering a bodyweight of 51.5 ± 8.5 kg, water ingestion rate of 4.05 L/d, and life expectancy of 63.7 yrs for an adult Indian reference man and compared with the reference dose (4.53 μg/kg/day). The average exposure level of U was comparatively high and the chemical toxicity was expected to be more. The mean of hazard quotient (LADD/ RfD) for all four districts was found to be greater than 1, indicating that groundwater may not be suitable for consumption from a chemical toxicity point of view.     

Implications of Using Steady-State Conditions in Estimating Dermal Uptake of Volatile Compounds in Municipal Drinking Water: An Example of THMs

Dermal exposure to volatile compounds (VC) in municipal water while showering is typically estimated using a steady-state condition between VC in water impacting on skin and skin exposed to water. The lag times to achieve steady-state between VC and skin can vary in the range of 7.5–218.3 min, while shower duration is often less than these values. Estimates of dermal exposure to VC using steady-state while showering may misinterpret exposure. This study developed models and estimated exposure to some disinfection byproducts (DBPs) through dermal pathway by considering lag times while showering. Dermal uptakes of VC were compared using different approaches. In the proposed approach, uptakes of trihalomethanes were estimated between 9.55 × 10^?10–1.43 × 10^?8 mg/cm² of skin during the lag times from exposure to water with trihalomethanes of 50 μg/L. These values were higher than the steady-state estimates (1.37 × 10^?10–4.34 × 10^?9 mg/cm²), and lower than the average exposure analysis (4.12 × 10^-8–1.93 × 10^?6 mg/cm²). Using the Drinking Water Surveillance Program data in Ontario, chronic daily intakes of trihalomethanes were estimated to be 9.40 × 10^?7 (1.85 × 10^?7–1.65 × 10^?6), 3.89 × 10^?6 (7.11 × 10^?7–2.33 × 10^?5), and 1.40 × 10^?6 (4.0 × 10^?7–1.77 × 10^?6) mg/kg/day in Toronto, Ottawa, and Hamilton, respectively. The findings can be useful in understanding THMs exposure and risk through dermal pathway.     

GIS based evaluation of fluoride contamination and assessment of fluoride exposure dose in groundwater of a district in Uttar Pradesh,India

Groundwater is the main source of drinking water in both rural and urban areas of the Pratapgarh district in the eastern Uttar Pradesh. Fifty-five groundwater samples were collected from 17 blocks of the Pratapgarh district and analyzed for fluoride (F^?) and other water quality parameters (pH, EC, TDS, turbidity, Cl^?, HCO₃^?, SO₄^2?, NO₃^?, Ca²⁺, Mg²⁺, Na⁺, K⁺, silica and total hardness) to assess its suitability for drinking uses. The fluoride concentration in the analyzed groundwater of the Pratapgarh district varied between 0.41 and 3.99 mg/L. Fluoride concentration in about 78% of the groundwater samples exceeded the acceptable level of 1.0 mg/L, while in 70% samples it exceeded the maximum permissible limit of 1.5 mg/L. A geographic information system (GIS) tool was used to study the spatial variation of fluoride concentrations in the groundwater of the Pratapgarh district. Fluoride is positively correlated with pH (0.36) and HCO₃^? (0.22) and negatively with Ca²⁺ (?0.23) and Mg²⁺ (?0.08), suggesting dissolution of fluoride-bearing minerals with the precipitation of Ca/Mg carbonate in the alkaline environment. The maximum exposure dose to fluoride for adults in the study area was found to be 6.8 times higher than the minimum risk level (MRL) of 0.05 mg kg^?1 day^?1 estimated by the Agency for Toxic Substances and Disease Registry (ATSDR).     

Trihalomethanes in desalinated water: Human exposure and risk analysis

Desalinated seawater is used to satisfy domestic water demands in many countries. The treated freshwater is blended with desalinated water to increase the water supply. The desalinated and blended water contains disinfection byproducts (DBPs), some of which may induce cancer risk to human. In this study, concentrations of trihalomethanes (THMs) in desalinated and blended water in Saudi Arabia were investigated, and human exposure and risk were predicted. The intakes of THMs (chloroform, bromodichloromethane, dibromochloromethane, and bromoform) were predicted to be 8.38 × 10^?5, 7.57 × 10^?5, 2.54 × 10^?5, and 4.32 × 10^?4 mg/kg-d, respectively. The overall cancer risk and hazard index were estimated to be 1.78 × 10^?5 (range: 7.40 × 10^?7–9.26 × 10^?5) and 3.49 × 10^?2 (range: 1.20 × 10^?3–2.34 × 10^?1), respectively. The probabilities of cancer risk exceeding the risk levels of 1 × 10^?6, 1 × 10^?5, and 5.0 × 10^?5 were 1.0, 0.775, and 0.012, respectively. The loss of disability adjusted life years (DALYs) was predicted to be 25.1 per year while the cancer risk represented 8.48 × 10^?7 DALY per person per year. The financial burden from such risk was estimated to be US$ 2.72 (range: US$ 2.52–2.91) million per year. The findings may assist in better understanding and reducing cancer risk from DBPs in desalinated and blended water.     

USE OF NATIVE PLANTS FOR REMEDIATION OF TRICHLOROETHYLENE: II. CONIFEROUS TREES

The phytoremediation of trichloroethylene (TCE) from contaminated groundwater has been extensively studied using the hybrid poplar tree (Populus spp.). Several metabolites of TCE have been identified in the tissue of poplar including trichloroethanol (TCEOH) and dichloroacetic acid (DCAA) and trichloroacetic acid (TCAA). In addition to the use of hybrid poplar for the phytoremediation of TCE, it is important to screen native tree species that could be successful candidates for field use. This study involves a greenhouse-based comparison of four different native southeastern conifers to a hybrid poplar species for their potential to phytoremediate TCE through the analysis of various plant tissues for TCE and major TCE metabolites, as well as several growth parameters that are desirable for phytoremediation. Longleaf pine (Pinus palustris), Leyland cypress (X Cupressocyparis leylandii), two varieties of Loblolly pine (Pinus taeda), and hybrid poplar species H11-11 (Populus trichocarpa x deltoides) were examined for the concentration of TCE and its metabolites in their tissue following treatment with either a low (50 mg L^?1) or high dose of TCE (150 mg L^?1) for 2 mo. The amount of water taken up, change in height of the tree, TCE transpiration, and total fresh weight of various tissue types were also measured. All trees contained detectable levels of TCE in their root and stem tissue. TCEOH was found only in the tissue of longleaf pine, suggesting that TCE metabolism was occurring in this tree. TCAA was only detected in the leaves of hybrid poplar and piedmont loblolly pine. Conifers took up less water over the 2-mo treatment period than hybrid poplar and grew at a slower rate. However, phytoremediation field sites may benefit from the evergreen's ability to transpire water throughout the winter months.     

Estimation of Excess Cancer Risk on Time-Weighted Lifetime Average Daily Intake of PAHs from Food Ingestion

The purposes of this study were to quantify the time-weighted, lifetime average, daily intake (LADI) of polycyclic aromatic hydrocarbons (PAHs) through food ingestion and to estimate the excess cancer risk based on lifetime dietary PAH intake. Twenty-seven different food commodities were selected from the 2001 Korean National Health and Nutrition survey based on their frequent consumption and high PAH level. The foods were analyzed for the profile of 14 PAH congeners using high performance liquid chromatography (HPLC) and fluorescence detector. Considering the toxic equivalent (TEQ) level converted with the toxic equivalent factors (TEFs), the highest total TEQ level of PAHs in foods was detected from roasted laver at 1.2 ug TEQ/kg. For the PAH exposure assessment according to ingested foods, the average body weight was separated according to the following age groups, 1–6, 7–19, 20–64 and over 64 years, and the daily food ingestion rates from the National Health and Nutrition survey were used. The estimated Lifetime Average Daily Intake (LADI) of PAHs was 3.22 × 10^–3 ug/kg/day for carcinogenic effects and was higher in the younger age groups under 20 years old than in the older groups. The dietary excess cancer risk estimated using the cancer potency of benzo(a)pyrene (7.3(mg/kg/day)^?1) was 2.3 × 10^?5, which is equivalent to a probability of tumor eruption in the upper gastrointestinal tract of two per hundred thousand persons.     

An integrated model for assessing the risk of TCE groundwater contamination to human receptors and surface water ecosystems

The practical implementation of the European Water Framework Directive has resulted in an increased focus on the hyporheic zone. In this paper, an integrated model was developed for evaluating the impact of point sources in groundwater on human health and surface water ecosystems. This was accomplished by coupling the system dynamics-based decision support system CARO-PLUS to the aquatic ecosystem model AQUATOX using an analytical volatilization model for the stream. The model was applied to a case study where a trichloroethylene (TCE)-contaminated groundwater plume is discharging to a stream. The TCE source will not be depleted for many decades; however, measured and predicted TCE concentrations in surface water were found to be below human health risk management targets. Volatilization rapidly attenuates TCE concentrations in surface water. Thus, only a 30-m stream reach fails to meet surface water quality criteria. An ecological risk assessment found that the TCE contamination did not impact the stream ecosystem. Uncertainty assessment revealed hydraulic conductivity to be the most important site-specific parameter. These results indicate that contaminant plumes with μg L^?1 concentrations of TCE entering surface water systems may not pose a significant risk.     

Indoor intake fraction considering surface sorption of air organic compounds for life cycle assessment

Purpose

Life cycle assessment (LCA) has largely focused on characterizing the impact of outdoor emissions. However, the intake fraction (iF) of indoor air emissions could be more important. The present paper aims to determine the long-term intake fractions of indoor emissions, including multiple indoor removal pathways such as sorption on indoor surfaces, and to compare it to the outdoor intake fraction.

Method

The developed model accounts for the different removal pathways in buildings, including air exchange, degradation in the gas phase, degradation on surfaces, and finally partitioning between air, walls, and furniture assuming a kinetically limited material transfer between gas phase and a near-surface film. The indoor intake fraction is presented as a function of the adsorption and degradation rate on surfaces.

Results and discussion

The intake fraction of volatile substances is only affected by the ventilation rate, with a constant intake fraction of 1?×?10^?2. For ozone-sensitive substances, indoor gas phase reactions can significantly reduce the intake fraction. Semi-volatile substances are affected by the adsorption and degradation on room surfaces. For highly adsorbing substances, the decrease in intake fraction is limited to a minimum value of 2.5?×?10^?4 by the mass transfer rate between air and room surfaces for a typical office or residence room in developed countries with temperate climate. Indoor intake fraction is compared to outdoor intake fraction calculated using the Impact 2002 multimedia model. Typical calculated indoor intake fraction values are in a significantly higher range (2.5?×?10^?4 to 1?×?10^?2) than inhalation outdoor values (1?×?10^?9 to 1?×?10^?6).

Conclusions

This paper opens new possibilities to assess the health impact of indoor and outdoor air emissions in a consistent way, including surface sorption??a major removal pathway for semi-volatile compounds. By combining the newly calculated intake fractions with effect factors and with indoor and outdoor emissions per functional unit, it becomes possible to consistently account for indoor exposure in methods such as LCA     

Remediation of Explosive-Contaminated Soils: Alkaline Hydrolysis and Subcritical Water Degradation

Alkaline hydrolysis and subcritical water degradation were investigated as ex-situ remediation processes to treat explosive-contaminated soils from military training sites in South Korea. The addition of NaOH solution to the contaminated soils resulted in rapid degradation of the explosives. The degradation of explosives via alkaline hydrolysis was greatly enhanced at pH ≥12. Estimated pseudo-first-order rate constants for the alkaline hydrolysis of 2,4-dinitrotoluene (DNT), 2,4,6-trinitrotoluene (TNT) and hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX) in contaminated soil at pH 13 were (9.6?±?0.1)×10^?2, (2.2?±?0.1)×10^?1, and (1.7?±?0.2)×10^?2 min^?1, respectively. In the case of subcritical water degradation, the three explosives were completely removed at 200–300°C due to oxidation at high temperatures and pressures. The degradation rate increased as temperature increased. The pseudo-first-order rate constants for DNT, TNT, and RDX at 300°C were (9.4?±?0.8)×10^?2, (22.8?±?0.3)×10^?2, and (16.4?±?1.0)×10^?2, respectively. When the soil-to-water ratio was more than 1:5, the extent of alkaline hydrolysis and subcritical water degradation was significantly inhibited.     

Perturbation of the tris(2,2′‐bipyridine) ruthenium(II)‐catalyzed Belousov–Zhabotinsky oscillating chemiluminescence reaction by l‐cysteine and its application

Perturbation of the tris(2,2′‐bipyridine)ruthenium(II) [Ru(bpy)₃²⁺]‐catalyzed Belousov–Zhabotinsky (BZ) oscillating chemiluminescence (CL) reaction induced by l ‐cysteine was observed in the closed system. It was found that the CL intensity was decreased in the presence of l ‐cysteine. Meanwhile, oscillation period and oscillating induction period were prolonged. The sufficient reproducible induction period was used as parameter for the analytical application of oscillating CL reaction. Under the optimum conditions, the changes in the oscillating CL induction period were linearly proportional to the concentration of l ‐cysteine in the range from 8.0 × 10^?7 to 5.0 × 10^?5 mol L^?1 (r = 0.997) with a detection limit of 4.3 × 10^?7 mol L^?1. The possible mechanism of l ‐cysteine perturbation on the oscillating CL reaction was also discussed. Copyright © 2009 John Wiley & Sons, Ltd.     

Spatial distribution,exposure, and potential health risk assessment from nitrate in drinking water from semi-arid region of South India

Abstract

Elevated nitrate concentration in groundwater is a worldwide problem. Continuous exposure to high levels of nitrate in groundwater may cause adverse health effects among residents who use groundwater for consumption. Therefore, this study was conducted to identify the nitrate distribution and its potential health risk assessment from semi-arid region of Peddavagu in Central Telangana (PCT), South India. Groundwater samples were collected from thirty five locations and analyzed for nitrate and other water quality parameters. Nitrate (NO₃^-) in groundwater was observed to vary from 17 to 120?mg/L, with a mean of 58.74?mg/L. About 57% of samples exceeded the maximum acceptable limit of Indian drinking water standard. About, 40% of groundwater samples drinking water quality index (DWQI) is good, while 60% of groundwater falls in poor quality for drinking purposes. Health risk maps were created based on hazard quotient to quantify the potential health risk of the residents using US Environmental Protection Agency (US EPA) health risk assessment model. Health risk assessment revealed that mean total hazard index (HI_total) for men, women, and children were found as 1.42E?+?00, 1.67E?+?00, and 1.95E?+?00, respectively. Results exhibited that children are at high health risk than men and women in the PCT. Further, the human exposure to the NO₃^- contaminated water was above the critical limit of non-carcinogenic risk.     

Characterization of metal(loid)s in indoor and outdoor PM2.5 of an office in winter period

The characterization of indoor (a naturally ventilated office) and outdoor (adjacent courtyard) metals in PM_2.5 during a winter period in Xi'an, China were carried out. The results indicated that the average mass concentrations of PM_2.5 in indoor and outdoor environments all exceeded the daily average limit of 75 µg m^–3 set by the Chinese government. The dominant metals in PM_2.5 were Ca, Al, Zn, Mg, Fe, and Pb in both indoor and outdoor air. Concentration of As was much higher than the standard of 6 ng m^–3 issued by the government. Enrichment factor analysis showed that anthropogenic emissions might be the primary sources of As, Cd, Pb, and Zn, while crust was the main origin of Co. A majority of indoor-to-outdoor concentration ratios of metal were lower than 1 indicating mostly the contribution of outdoor sources rather than indoor ones. As and Cr in both indoor and outdoor air posed the highest noncarcinogenic and carcinogenic risks, respectively. The noncarcinogenic and carcinogenic risks were 2.74 and 2.54 × 10^?4 indoor and 4.04 and 3.87 × 10^?4 outdoor, which suggested that possible adverse health effects should be of concern.     

Abscisic Acid-Induced Starch Accumulation in Bioenergy Crop Duckweed <Emphasis Type="Italic">Spirodela polyrrhiza</Emphasis>

Spirodela polyrrhiza, a fast-growing duckweed with high starch and low lignin content, shows promise as a feedstock for bioenergy. Abscisic acid (ABA) is a biological hormone that controls plant growth and stress response. The effects of different ABA concentrations (0, 1.0 × 10^?5, 1.0 × 10^?4, 1.0 × 10^?3, 1.0 × 10^?2, and 1.0 × 10^?1 mg/L) on duckweed biomass growth, carbon dioxide fixation, formation of photosynthetic pigments (Chlorophyll a (Chla), Chlorophyll b (Chlb), and carotenoids), the activities of soluble starch synthase (SSS) and starch branching enzyme (SBE), and the starch content of biomass were investigated in this study. ABA at concentrations lower than 1.0 × 10^?3 mg/L promoted carbon dioxide fixation, whereas it inhibited carbon dioxide fixation at concentrations over 1.0 × 10^?3 mg/L. ABA enhanced SSS and SBE activities at concentrations lower than 1.0 × 10^?2 mg/L. ABA treatment increased the content of Chla, Chlb, and carotenoids and resulted in the enhancement of starch content. Chla content gradually increased with the increasing concentration of ABA (1.0 × 10^?5 to 1.0 × 10^?2 mg/L). After culturing for 10 days, starch content in 1.0 × 10^?2 mg/L ABA medium reached 35.3% of dry weight (DW), which was the highest level in this study. This suggests that there is a great potential to develop a technology to increase starch accumulation in duckweed which can be used as an alternative to corn, sugarcane, or other food crops as a starch source.