Triclosan In Sediments Research Articles

Accumulation and Risk of Triclosan in Surface Sediments Near the Outfalls of Municipal Wastewater Treatment Plants.

Triclosan is an antimicrobial agent which is widely used in many personal care products. This toxic chemical is frequently found in the aquatic environment. The municipal wastewater treatment plant (WWTP) effluent has been reported to be one of the major sources for triclosan in the aquatic system. The aim of the present study was to investigate the accumulation of triclosan in the surface sediments near the outfalls of the five major municipal WWTPs of Nanjing, China, as well as to evaluate its potential ecological risk. The concentration of triclosan in the sediment samples ranged from 48.3 to 226ng/g dry weight, which was well correlated with the acute and genetic toxicity by bioassay. The results suggested that triclosan released from municipal WWTPs could accumulate in the surface sediments nearby and may pose undetermined risk to aquatic organisms.

Sorption/desorption behavior of triclosan in sediment–water–rhamnolipid systems: Effects of pH, ionic strength, and DOM

Effects of pH, ionic strength and DOM on the sorption and desorption of triclosan (TCS) in sediment–water–rhamnolipid systems were systematically investigated through controlled batch experiments. Results showed that solubilization enhancement of TCS by rhamnolipid was higher in acid pH range than in alkaline pH range and was the highest at the ionic strength of 5×10−2M. Sorption of rhamnolipid onto sediment decreased with the increase of pH while the result was contrary to ionic strength. Moreover, the apparent distribution coefficients of TCS (Kd*) decreased from 73.35 to 32.30L/kg with an increase of solution pH, as varying pH had significant influence on sorption of RL onto sediment and degree of ionization of TCS. Rhamnolipid presented the largest distribution capacity of TCS into the aqueous phase at moderate ionic strength (5×10−2M) with the Kd* of 17.26L/kg. Further results also indicated that the presence of humic acid in aqueous phase could increase the desorption of TCS from contaminated sediment. The desorption enhancement was much higher in the system containing both rhamnolipid and DOM than in the single system. These findings provide meaningful information for enhanced migration of TCS from sediment to water by rhamnolipid.

Sorption and degradation of triclosan in sediments and its effect on microbes

Sorption and degradation behavior of triclosan (TCS) and its effect on microbes were studied in three sediments spiked at different concentration levels (1, 10, and 100μgg−1). TCS showed a strong affiliation to all the sediments with linear adsorption coefficients (Kd) that varied from 220 to 1092Lg−1, and the adsorption capacity is related to the total organic carbon (TOC) contents of the sediments. The half-lives of TCS varied from 55 to 239 days, and were longer in sediment with higher Kd. TCS showed minor effect on the activities of fluorescein diacetate hydrolase, dehydrogenase, alkaline phosphatase, and urease in the 1μgg−1 treatment, but at higher levels, a short-term effect was observed followed by a rapid recovery except the urease activity in sediment with the lowest adsorption capacity. PCA plots of phospholipid fatty acid showed that the phenotypic community in sediments with low TOC were more sensitive to TCS. A positive relation between bacterial biomass and total microbial biomass suggests that changes of bacteria biomass were responsible for changes of total microbial biomass in treatments. Denaturing gradient gel electrophoresis analysis of the 16S rDNA showed that the bacterial community structure deviated further away from the control at higher TCS concentration levels, with similarity coefficients in Un-weighted Pair Group Mathematics Average clustering between control and 100μgg−1 treatment varied from 0.38 to 0.73. Both degradation rate and toxic effects of TCS decreased in sediment with higher sorption capacity, which can be attributed to a reduced bioavailablity.

Occurrence of triclosan in the tropical rivers receiving the effluents from the hospital wastewater treatment plant.

The objective of this study was to determine the occurrence of triclosan in the tropical rivers where received the effluents from a hospital wastewater treatment plant (HWWTP) in southern Taiwan. Three and ten sampling sites were selected at the Jiaosu River (S0-S2) and Dian-Bao River (S3-S12), respectively. The samples of the HWWTP influent, effluent and receiving river water and sediment were collected and analyzed using ultrahigh-performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/ MS). Results showed that the triclosan level in surface water of the Jiaosu River and Dian-Bao River ranged from 3 to 68 ng/L and ranged from <2.7 to 51 ng/L, respectively. The hospital did contribute a loading of triclosan to the neighboring river. The mean value of triclosan concentration in the downstream surface water of the Jiaosu River (S1 20.2 ng/L) was approximately three times higher than that of the background level (S0 6.0 ng/L) (p = 0.011). The concentrations of triclosan in two surface water samples were over the predicted no effect concentration (PNEC) of 50 ng/L for algae. In addition, significant seasonal differences of triclosan in surface water of Jiaosu River (p = 0.020) and the HWWTP effluents (p = 0.302) were also observed. The concentrations of triclosan in sediments of these two rivers seemed stable. On average, triclosan was detected in 86 % of the sediment samples with a range from <1.1 to 13 ng/g. Triclosan in surface water and sediments of the tropical rivers might be rapidly photolyzed due to plenty of sunshine. It is worth to further investigate the occurrence and fate of triclosan photoproduct in the aquatic environment of the tropics.

Biocides in the Yangtze River of China: Spatiotemporal distribution, mass load and risk assessment

Nineteen biocides were investigated in the Yangtze River to understand their spatiotemporal distribution, mass loads and ecological risks. Fourteen biocides were detected, with the highest concentrations up to 166 ng/L for DEET in surface water, and 54.3 ng/g dry weight (dw) for triclocarban in sediment. The dominant biocides were DEET and methylparaben, with their detection frequencies of 100% in both phases. An estimate of 152 t/y of 14 biocides was carried by the Yangtze River to the East China Sea. The distribution of biocides in the aquatic environments was significantly correlated to Gross Domestic Product (GDP), total phosphorus (TP) and total nitrogen (TN), suggesting dominant input sources from domestic wastewater of the cities along the river. Risk assessment showed high ecological risks posed by carbendazim in both phases and by triclosan in sediment. Therefore, proper measures should be taken to reduce the input of biocides into the river systems.

Occurrence, distribution, and multi-phase partitioning of triclocarban and triclosan in an urban river receiving wastewater treatment plants effluent in China

Occurrence, distribution, spatial and seasonal variations, and partitioning between aqueous phase and suspended particulate matters (SPM) of triclocarban (TCC) and triclosan (TCS) in Xiaoqing River, which receives wastewater treatment plant (WWTP) effluents, were studied. The distribution of the total TCC and TCS levels in surface water and sediments along the river were discussed. The highest TCC and TCS concentrations were both found near the discharge port of WWTPs, and the TCC and TCS levels decreased downstream of the WWTPs as a result of their distances from the source of WWTP discharges. The mean values of TCC and TCS in low-flow season were 1.62 and 1.80 times, respectively, as much as in high-flow season in surface water. The study on partitioning of TCC and TCS between aqueous phase and SPM shown the mean level of dissolved TCC accounted for about 10 % of the total level in surface water, whereas the TCS level was about 30 %. The TCC concentrations detected in the surface sediment samples (0 to 5 cm) ranged from 226 to 1,956 ng/g, with a mean value of 733 ng/g. The TCS levels were between 85 and 705 ng/g, with a mean value of 255 ng/g. The distribution and variations of TCC and TCS in sediments along the river were highly consistent with those in the water phase. The TCC and TCS levels in deep sediments (5 to 10 cm) were significantly lower than those in surface sediments. The mean TCC level in surface sediments was about 2.4 times as much as in deep sediments, and the TCS level in surface sediments was 3.1 times as much as in deep sediments.

Effects of monorhamnolipid and dirhamnolipid on sorption and desorption of triclosan in sediment–water system

The effects of monorhamnolipid (RL-F1) and dirhamnolipid (RL-F2) on the sorption and desorption of triclosan (TCS) in sediment–water system were investigated in this study. Results of the bath equilibrium experiments showed that RL-F2 provided much higher solubilization enhancement for TCS than RL-F1. Sorption of both rhamnolipids by the sediments was highly correlated with the sediment clay content. Moreover, the apparent distribution coefficients of TCS Kd∗ decreased with the increase of rhamnolipid concentration (0.05–7.5mM), and RL-F2 presented a larger distribution capacity of TCS into the aqueous phase at relatively higher concentrations (>2.5mM). Further results also indicated that the release of TCS from sediment could be enhanced by both rhamnolipids. RL-F2 was more efficient than RL-F1 in desorbing TCS from the sediment with low clay content. The TCS desorption percentages Rd∗ of RL-F2 (5mM) was 1.8–2.4 times that of RL-F1. These findings could provide useful guidelines for the application of rhamnolipid-enhanced remediation technologies for TCS contaminated sediment.

Probabilistic risk evaluation for triclosan in surface water, sediments, and aquatic biota tissues

Triclosan, an antimicrobial compound used in personal care products, occurs in the aquatic environment due to residual concentrations in municipal wastewater treatment effluent. We evaluate triclosan-related risks to the aquatic environment, for aquatic and sediment-dwelling organisms and for aquatic-feeding wildlife, based on measured and modeled exposure concentrations. Triclosan concentrations in surface water, sediment, and biota tissue are predicted using a fugacity model parameterized to run probabilistically, to supplement the limited available measurements of triclosan in sediment and tissue. Aquatic toxicity is evaluated based on a species sensitivity distribution, which is extrapolated to sediment and tissues assuming equilibrium partitioning. A probabilistic wildlife exposure model is also used, and estimated doses are compared with wildlife toxicity benchmarks identified from a review of published and proprietary studies. The 95th percentiles of measured and modeled triclosan concentrations in surface water, sediment, and biota tissues are consistently below the 5th percentile of the respective species sensitivity distributions, indicating that, under most scenarios, adverse affects due to triclosan are unlikely.

Probabilistic risk evaluation for triclosan in surface water, sediments, and aquatic biota tissues

AbstractTriclosan, an antimicrobial compound used in personal care products, occurs in the aquatic environment due to residual concentrations in municipal wastewater treatment effluent. We evaluate triclosan‐related risks to the aquatic environment, for aquatic and sediment‐dwelling organisms and for aquatic‐feeding wildlife, based on measured and modeled exposure concentrations. Triclosan concentrations in surface water, sediment, and biota tissue are predicted using a fugacity model parameterized to run probabilistically, to supplement the limited available measurements of triclosan in sediment and tissue. Aquatic toxicity is evaluated based on a species sensitivity distribution, which is extrapolated to sediment and tissues assuming equilibrium partitioning. A probabilistic wildlife exposure model is also employed, and estimated doses are compared to wildlife toxicity benchmarks identified from a review of published and proprietary studies. The 95th percentiles of measured and modeled triclosan concentrations in surface water, sediment, and biota tissues are consistently below the 5th percentile of the respective species sensitivity distributions, indicating that under most scenarios adverse affects due to are unlikely. © 2010 SETAC