Bisphenol A In Sediments Research Articles

Occurrence, source apportionment and ecological risk of bisphenol analogues in river sediments in areas with different land use patterns

Bisphenol analogues (BPs) have gained increasing attention in recent years due to their ubiquitousness and potential endocrine disrupting properties in environments. However, little information is available on their spatiotemporal distribution, source apportionment and ecological risk in river sediments, especially the case in river basins with a high population density and those typical regions with agricultural-urban gradient, where land use patterns and intensity of human activity are varying. In this study, field investigations of BPs in the sediment of the entire Qinhuai River Basin, a typical agricultural-suburban agricultural-urban gradient area, were conducted before and after the flood period. Thirty-two sites were sampled for six types of BPs, resulted in no significant difference in the concentration of ΣBPs between the two periods, with ΣBPs ranging from 3.92 to 151 ng/g and 2.16–59.0 ng/g, respectively. Bisphenol A (BPA) was the main contributor. Whereas a multivariate analysis of variance (MANOVA) suggested that the composition structure of BPs had been influenced by water periods. The land use patterns had an impact on the distribution of ΣBPs in river sediments, which was more significant in after the flood period, with ΣBPs in urban rivers was 1.85 times, 3.44 times, and 3.08 times higher than the suburban rivers, agricultural rivers, and reservoirs, respectively. Yet land use types did not significantly alter the composition structure of BPs. The correlation analysis between BPs and the physicochemical properties of sediments showed a significant positive correlation between BPA and total organic carbon (TOC). The positive matrix factorization model (PMF) suggested that BPs in sediments of the basin might be influenced by industrial coatings, textiles, electronics and biopharmaceuticals, as well as urban wastewater or solid waste generated from daily life. The ecological risk assessment posed by BPA, based on the risk quotient, indicated that the ecological risk of BPA in sediments was low for three indicator benthic organisms: crustaceans, worms, and mollusks. However, the risk of BPA in river sediments varied among different land use patterns, with the risk ranking as follows: reservoirs < agricultural rivers < suburban rivers < urban rivers.

Presence and quantification of the microplastics and bisphenol-A in sediments along the Guanabara Bay, Brazil

Microplastics (MP) and endocrine disruptors, such as bisphenol-A (BPA) have both become significant environmental concerns worldwide, although assessments in estuarine environments are still scarce. In this regard, Guanabara Bay is one of the most important Brazilian estuarine systems, displaying significant economic and environmental relevance, although it has suffered increasing anthropogenic effects for decades. Thus, this study aimed to assess the occurrence of both MP and BPA in the sediments of this estuarine system though stereomicroscope identification and high-performance liquid chromatography. Both pollutants were detected in all sediment samples. A total of 3 to 11 MP particles (&lt;5 mm) per 50 cm2 were detected, higher than in other studies worldwide. MPs were categorized as fibers and fragments, mostly green, possibly from fisher rope and net degradation. BPA ranged from 0.36 to 19.75 ng g-1, higher near Governador Island and the Rio de Janeiro harbor. Potential correlations between MPs and BPA, however, could not be determined. Both MP and BPA represent significant environmental concerns in the already highly impacted Guanabara Bay estuarine system, and further assessments are paramount to understand potential ecotoxicological hazards associated to these pollutants.

Distribution of Bisphenol A in Sediment and Suspended Matter and Its Possible Impact on Marine Life in Kaštela Bay, Adriatic Sea, Croatia

Over the last decade, bisphenol A (BPA) has become a chemical of concern in the marine environment. There is little data on BPA levels in the eastern Adriatic Sea, Croatian waters. This study provides concentrations of BPA in marine sediments and suspended matter sampled from the Kaštela Bay (the central part of the Adriatic Sea) for two years. The results obtained show that BPA in sediment samples ranged from 1.05 to 46.31 µg kg−1, while they were higher in the suspended matter, ranging from 1.84 to 81.39 µg kg−1. To demonstrate a possible correlation between BPA concentrations and other parameters in sediment and suspended matter, the granulometric composition and organic matter content were determined. There was no correlation between BPA and investigated sediment characteristics. To assess the possible effects of BPA on marine biota, its possible estrogenic effect was also investigated by calculating estradiol equivalent concentration (EEQ, µg kg−1), the maximum value of which, in this study, was 0.0181 µg kg−1 in the sediment samples and 0.0317 µg kg−1 in suspended matter samples. Based on the presented results, it is unlikely that BPA could cause significant endocrine disruption to marine life in the study area.

Adsorption and removal of bisphenol A in two types of sediments and its relationships with bacterial community

Bisphenol A (BPA) as an endocrine-disrupting chemical has been widely detected in the aquatic environment, including Taihu Lake, China. Adsorption and bacterial removal in sediments play important roles in the fate of BPA in the aquatic environment, which might be influenced by the properties of the sediment. In this study, two types of sediments from Gonghu Bay and Meiliang Bay in the northern Taihu Lake were collected to investigate the fate of BPA in the sediments. Both sediments showed different adsorption properties to BPA. Due to the higher proportion of sand and total organic carbon (TOC) content in the Meiliang Bay sediment, its adsorption capacity was stronger than that in the Gonghu Bay sediment. Bacteria in both sediments could completely degrade BPA within 3–5 days. Based on the correlation analysis, Firmicutes and Cyanobacteria might be involved in BPA removal at the phyla level. At the genus level, Novosphingobium, Massilia, and Methylophilus were found to be related to the BPA removal in the Gonghu Bay sediment, and Acinetobacter, Bacillus and Pseudomonas were found in the Meiliang Bay sediment. The different bacterial communities might be important reasons for the different removal capacity of BPA in both sediments. The above results provide basic information for the assessment and management of BPA in the Taihu Lake, and improve the understanding of BPA removal in sediments.

Typical Endocrine Disrupting Compounds in Rivers of Northeast China: Occurrence, Partitioning, and Risk Assessment.

Liao River Basin (LRB), located in northeast China, is one of seven largest river basins in China. The Daliao River Watershed (DLRW) is severely disturbed by human activities in the LRB. In this study, three rivers within the DLRW-Xi River (XR), Hun River (HR), and Daliao River (DLR)-were selected as sampling locations. The distribution, partitioning, and risk assessment of four endocrine-disrupting compounds (EDCs), e.g., bisphenol A (BPA), 17β-estradiol (E2), estrone (E1), and 17α-ethinyl estradiol (EE2), in the rivers were investigated. The results showed that the concentration of BPA was generally higher than those of the other three steroidal estrogens in the sampling locations. The estrogen levels in the XR were greater than those in the HR and DLR. As a result of a decreasing river flow rate during the frozen season and irregular wastewater discharge from human domestic activities and manufacture processing, the total concentration of selected EDCs in the frozen season was much greater than those in nonfrozen season with the highest concentration in surface water of the XR at 1131.0ng/L for BPA, 1235.0ng/L for E1, 1253.5ng/L for E2, and 17,111.5ng/L for EE2, respectively. Based on the field-measured BPA concentrations in the sediment and water, the organic carbon-normalized partition coefficient (K oc) of BPA were calculated with the values of 2884-45,031L/kg; the concentration of BPA in sediment was positive correlated with the content of OC (R 2=0.932). The risk assessment made by estradiol equivalent (EEQ) and risk quotient (RQ) showed that 64.7% of sampling sites were exposed to high estrogenic activity (∑EEQ>1) and high risk in surface water, whereas the RQ values of all selected estrogens in sediment were in medium or minimal risk. Both EE2 and E1 were the major contributors to the total estrogenic activity and risk quotient in surface water.

Identification of 4-Hydroxycumyl Alcohol As the Major MnO2-Mediated Bisphenol A Transformation Product and Evaluation of Its Environmental Fate.

Bisphenol A (BPA), an environmental contaminant with weak estrogenic activity, resists microbial degradation under anoxic conditions but is susceptible to abiotic transformation by manganese dioxide (MnO2). BPA degradation followed pseudo-first-order kinetics with a rate constant of 0.96 (±0.03) min(-1) in the presence of 2 mM MnO2 (0.017% w/w) at pH 7.2. 4-hydroxycumyl alcohol (HCA) was the major transformation product, and, on a molar basis, up to 64% of the initial amount of BPA was recovered as HCA. MnO2 was also reactive toward HCA, albeit at 5-fold lower rates, and CO2 evolution (i.e., mineralization) occurred. In microcosms established with freshwater sediment, HCA was rapidly biodegraded under oxic, but not anoxic conditions. With a measured octanol-water partition coefficient (Log K(ow)) of 0.76 and an aqueous solubility of 2.65 g L(-1), HCA is more mobile in saturated media than BPA (Log K(ow) = 2.76; aqueous solubility = 0.31 g L(-1)), and therefore more likely to encounter oxic zones and undergo aerobic biodegradation. These findings corroborate that BPA is not inert under anoxic conditions and suggest that MnO2-mediated coupled abiotic-biotic processes may be relevant for controlling the fate and longevity of BPA in sediments and aquifers.

Adverse effects of bisphenol A on water louse (Asellus aquaticus)

Experiments were performed to study the effects of short and long-term exposure to bisphenol A (BPA) on a freshwater crustacean isopod Asellus aquaticus (L.). Two life stages of isopods were exposed to a range of BPA concentrations, from aqueous and two dietary sources, in the form of with BPA spiked conditioned alder leaf (Alnus glutinosa) discs, or spiked formulated sediment, to determine the relative importance of each source of exposure on the uptake of this contaminant. Several lethal and sublethal endpoints were evaluated in this study to measure the potential effects of BPA on A. aquaticus, including mortality, growth and feeding rate inhibition, mobility inhibition, de-pigmentation and molting disturbances. They signify a correlation to BPA levels and a difference in BPA uptake efficiency from different uptake sources. Results of acute exposure to BPA show a greater sensitivity of test systems using juvenile specimens with a 96h LC50 of 8.6mgL−1 BPA in water medium and a 96h LC50 of 13.5mgL−1 BPA in sediment. In comparison, adult isopods show a 96h LC50 of 25.1mgL−1 BPA in water medium and a 96h LC50 of 65.1mgL−1 BPA in sediment. Observed endpoints of chronic exposures suggest the alder leave discs to be the most efficient uptake source of BPA, in contrast to uptake from water or heterogeneous sediment. Significant (p<0.05) growth inhibition, with a 21d NOEC of 0.5/2.5mgL−1 (for juvenile/adult organisms), and feeding rate inhibition, with a 21d NOEC of 0.5/1.0mgL−1 (for juvenile/adult organisms), were proven to be the most sensitive toxicity endpoints. An even more sensitive effect turned out to be molting frequency, which was significantly reduced; a 21d NOEC was 1.0mgL−1 of BPA for adult organisms and an even lower 21d NOEC of 0.05mgL−1 of BPA for juveniles. The observed endpoints are recorded at very low, non-toxic exposure concentrations, indicating that BPA acts as an endocrine disrupting compound, as well as a toxic substance. We also determined the importance of the direct dietary uptake of the pollutants, significant for juveniles as well as adult animals.

Spatial and seasonal distributions of estrogens and bisphenol A in the Yangtze River Estuary and the adjacent East China Sea

Surface water and sediments in the Yangtze River Estuary (YRE) and the adjacent East China Sea (ECS) were sampled to investigate the spatial and seasonal distributions of Estrone (E1), 17β-estradiol (E2), 17α-ethinylestradiol (EE2) and bisphenol A (BPA). E1 and BPA were the dominant compounds detected. The zones of the highest E1 and BPA concentrations in water were located at the mouth of the Huangpu River and the outfalls of wastewater treatment plants. The zones of the highest concentrations in sediments were mainly located in the down reach of the estuary and the adjacent sea. The relationship between E1 and BPA in sediments with those in water was not significant (BPA: r=0.16, p=0.21; E1: r=0.18, p=0.24), but positive correlations with the total organic carbon (TOC) contents of sediments (BPA: r=0.57, p<0.01; E1: r=0.33, p=0.04) and negative correlations with the sand contents of sediments (BPA: r=−0.52, p<0.01; E1: r=–0.16, p=0.23) were found. The TOC contents were the major factor influencing the E1 and BPA distributions in sediments. The hierarchical cluster analysis further indicated the spatial distributions of BPA and E1 in sediments were obviously affected by TOC and sediment particle sizes, whilst the distributions varied slightly with seasons.

Trace organic contaminants in sediment and water from Ulsan Bay and its vicinity, Korea.

Sediment and water samples collected from 32 locations in Ulsan Bay and adjacent inland areas were analyzed for polycyclic aromatic hydrocabons (PAHs), nonylphenol (NP), octylphenol (OP), bisphenol A (BPA), organochlorine (OC) pesticides (HCB, HCHs, CHLs, and DDTs), and polychlorinated biphenyls (PCBs) to characterize their spatial distribution and contamination status. PAHs were detected in nearly all sediment and water extracts from Ulsan Bay and its inland locations. The sedimentary PAH concentrations ranged from 17 to 3,100 ng/g on a dry weight basis (DW), which were predominated by two- and three-ring aromatic hydrocarbons in river and/or stream, and four- to six-ring compounds in Ulsan Bay sediment. Concentrations of PAHs in pore water samples were generally two or three orders magnitude less than those of corresponding sediment samples. Maximum concentrations of NP, OP, and BPA in sediments were 1,040, 120, and 54 ng/g DW, respectively. Concentrations of OP and BPA were, on average, 5- to 13-fold less than those of NP. PCB concentrations in sediment ranged from 1.4 to 77 ng/g DW, which were predominated by lower chlorinated congeners such as di- through pentachlorinated biphenyls. Among different OC pesticides analyzed, concentrations of DDTs were the greatest, ranging from 0.02 to 41.9 ng/g DW. NP concentrations were greater at inner locations proximal to municipal wastewater discharges into rivers and/or streams, whereas the concentrations of PCBs and PAHs were great near the sites of high industrial activities. Sediment-pore water partitioning coefficients correlated with those of reported Koc or Kow values for selected PAHs in Ulsan Bay, but these varied by an order of magnitude for stream and/or river sediments.