Yungen Liu

Arsenic-hyperaccumulator Pteris vittata efficiently solubilized phosphate rock to sustain plant growth and As uptake

Phosphorus (P) is one of the most important nutrients for phytoremediation of arsenic (As)-contaminated soils. In this study, we demonstrated that As-hyperaccumulator Pteris vittata was efficient in acquiring P from insoluble phosphate rock (PR). When supplemented with PR as the sole P source in hydroponic systems, P. vittata accumulated 49% and 28% higher P in the roots and fronds than the -P treatment. In contrast, non-hyperaccumulator Pteris ensiformis was unable to solubilize P from PR. To gain insights into PR solubilization by plants, organic acids in plant root exudates were analyzed by HPLC. The results showed that phytic acid was the predominant (>90%) organic acid in P. vittata root exudates whereas only oxalic acid was detected in P. ensiformis. Moreover, P. vittata secreted more phytic acid in -P and PR treatments. Compared to oxalic acid, phytic acid was more effective in solubilizing PR, suggesting that phytic acid was critical for PR utilization. Besides, secretion of phytic acid by P. vittata was not inhibited by arsenate. Our data indicated that phytic acid played an important role in efficient use of insoluble PR by P. vittata, shedding light on using insoluble PR to enhance phytoremediation of As-contaminated soils.

Knocking Out OsPT4 Gene Decreases Arsenate Uptake by Rice Plants and Inorganic Arsenic Accumulation in Rice Grains

Arsenic (As) accumulation in rice grains poses health risk to humans. Plants including rice take up arsenate (AsV) by phosphate transporters. In this study, rice phosphate transporter OsPT4 (OsPht1;4) was investigated based on two independent T-DNA insertion mutants of OsPT4 (M1 and M2), which displayed stronger AsV resistance than wild types WT1 and WT2. When cultivated in medium (+P or -P) with AsV, ospt4 mutants accumulated 16-32% lower As in plants, suggesting that OsPT4 mediates AsV uptake. Analysis of the xylem sap showed that AsV concentrations in ospt4 mutants was 20-40% lower than WT controls under -P condition, indicating OsPT4 may also mediate AsV translocation. Moreover, kinetics analysis showed that ospt4 mutants had lower AsV uptake rates than the WT controls, further proving that OsPT4 functions as an AsV transporter in rice. When grown in flooded soils with As, AsV concentrations in rice grains of ospt4 mutants decreased by 50-55%. More importantly, knocking out OsPT4 in M1 and M2 reduced inorganic As accumulation in rice grains by 20-44%, significant for controlling As exposure risk from rice. Taken together, our findings revealed a critical role of OsPT4 in AsV uptake and translocation in rice. Knocking out OsPT4 effectively decreased inorganic As accumulation in rice grains, shedding light on engineering low-As rice to enhance food safety.

Metal concentrations in traditional and herbal teas and their potential risks to human health

Food and beverage consumption is an important route for human exposure to metals. Traditional tea (Camellia sinensis) is a widely-consumed beverage, which may contain toxic metals. This study determined total and infusion concentrations of 5 metals including Al, As, Cd, Cr, and Pb in 47 traditional and herbal teas from 13 countries and assessed their potential risks to human health. The data showed that herbal teas exhibited higher As (0.26mgkg-1), Cd (0.19mgkg-1) and Pb (2.32mgkg-1) than traditional teas. Black tea from India had high Cr at 31mgkg-1 while white tea from China had low Cr at 0.39mgkg-1. Arsenic, Cd and Pb did not exceed the WHO limit for medicinal plants excluding one herbal tea with 1.1mgkg-1 As and 26.4mgkg-1 Pb. However, Cr in 47% herbal teas and 73% traditional teas exceeded the Canada limit of 2mgkg-1. Metal concentrations in tea infusions were below the MCL for drinking water except for Al. Total Al and its infusion was lower in herbal teas (47-1745mgkg-1 and 0.09-3.95mgL-1) than traditional teas (50.3-2517mgkg-1 and 0.02-7.51mgL-1), with 0.9-22% and 4-49% of the Al being soluble in infusion. The Al concentrations in infusion in all black tea and 83, 75 and 25% of the green, oolong and herbal teas exceeded the secondary MCL for drinking water at 0.2mgL-1. However, the weekly intake of Al from drinking tea (0.001-0.39 and 0.003-0.56mgkg-1 for children and adults) was lower than the provisional tolerable weekly intake for Al at 1.0mgkg-1. Our data showed that it is important to consider metal intake from tea consumptions, especially for Cr and Al in heavy tea drinkers.

Interactive effects of chromate and arsenate on their uptake and speciation in Pteris ensiformis

Background and aimsArsenate (AsV) and chromate (CrVI) inhibit each other’s uptake and translocation in As-hyperaccumulator Pteris vittata. In the present study, we extended the research to As-sensitive plant Pteris ensiformis to better understand the mechanism of their interactions.MethodsPlants were exposed to 0, 0.75 or 7.5 mg L−1 AsV and 0, 0.52, or 5.2 mg L−1 CrVI for 7 d in hydroponics. Arsenic and Cr speciation were determined in nutrient solutions and plant biomass.ResultsP. ensiformis accumulated high levels of As and Cr in the rhizomes and roots with low levels in the fronds. However, P. ensiformis was much more effective in taking up Cr than As, as much more Cr was accumulated in the roots (306–6015 vs. 87–642 mg kg−1). AsV and CrVI increased each other’s uptake in the rhizomes and roots when co-present. The AsV and CrVI taken up by P. ensiformis were reduced to arsenite (AsIII) and chromite (CrIII), possibly serving as detoxification mechanism.ConclusionsUptake of As and Cr induced oxidative stress as indicated by increased lipid peroxidation and electrical conductivity. Arsenic and Cr increased each other’s uptake by P. ensiformis.

PAHs in urban soils of two Florida cities: Background concentrations, distribution, and sources

Polycyclic aromatic hydrocarbons (PAHs) are ubiquitous organic contaminants, which are found in soils throughout the U.S. The objective of this study was to determine the background concentrations, distributions, and sources of 16 USEPA priority PAHs in two urban soils. A total of 114 soil samples were collected from two large cities in Florida: Orlando and Tampa. The results showed that soils were dominated by high molecular weight PAHs in both cities. The average ∑16-PAHs in Orlando and Tampa soils were 3227 and 4562 μg kg-1, respectively. The averages of 7 carcinogenic PAHs based on the benzo[a]pyrene-equivalent (BaP-EQ) concentrations in the two cities were 452 and 802 μg kg-1. BaP-EQ concentrations in 60-62% of samples were higher than the Florida Soil Cleanup Target Level (FSCTL) for residential soils at 100 μg kg-1 and 20-25% of samples were higher than FSCTL for industrial soils at 700 μg kg-1. Based on molecular diagnostic ratios and PMF modeling, major sources of soil PAHs in both cities were similar, mainly from pyrogenic sources including vehicle emissions, and biomass and coal combustion. Based on ArcGIS mapping, PAH concentrations in soils near business districts and high traffic roads were higher. Thus, it is important to consider background PAH concentrations in urban soils when considering soil remediation.

Water extract of indoor dust induces tight junction disruption in normal human corneal epithelial cells

In corneal epithelium, tight junctions play a vital role in its barrier function. Human cornea is highly susceptible to damage by dust. Continued daily exposure to dust has been associated with increased risks of corneal injury. Studies demonstrated that water extract of dust induced cytotoxicity in human corneal epithelial cells (HCECs); however, its effects on corneal epithelial barrier function are unknown. In this study, we determined the concentrations of heavy metals in water extracts of dust, with office dust having higher concentrations of heavy metals than housedust, and Cu and Zn being highest among metals for both dust. Changes in barrier function and its associated mechanism after exposing HCECs to water extracts of dust at 48 μg/100 μ L for 7 d were evaluated. Water extracts of both dust caused decrease of TEER value (39-73%), down-regulation of gene expression related to tight junction and mucin (0.2-0.8 fold), and loss of ZO-1 immunoreactivity from cellular borders, with office dust having greater potential than housedust to disrupt corneal epithelial barrier function. Our data implied the importance to reduce heavy metals in dust to reduce their adverse impacts on human eyes.

Source identification of PAHs in soils based on stable carbon isotopic signatures

Abstract Polycyclic aromatic hydrocarbons (PAHs) are ubiquitous in the environment and some exhibit carcinogenic and mutagenic toxicity. Three methods have been used for identification of PAHs sources in soils, including molecular diagnostic ratios, receptor models, and stable C isotopic signatures, with stable C isotopic ratios based on δ13C values being underutilized. Isotopic fractionation effects occur after environmental transportation of PAHs such as deposition and burial. This characteristic makes this method useful in source identification. Here, we provided a comprehensive review of tracing sources of soil PAHs using stable C isotopic fingerprinting technique. Fractionation of C isotopes occurs during formation and degradation processes of PAHs, making them useful tools to trace sources of PAHs in soils. The fundamentals of δ13C measurement and compound-specific isotopic analysis to trace sources of soil PAHs are summarized. Furthermore, for the first time, the biogeochemical cycle and contamination source evaluation based on δ13C signatures for soil PAHs are proposed. In addition, radioactive C isotope and stable H isotope ratios of PAHs are also briefly introduced as supplementary techniques. In short, these methods offer much promise, but still need work to fill in knowledge gaps. Establishing a C isotopic signature database to expand the utilization of this technique for tracing PAHs in soils is needed.