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The vertical distribution, level of contamination, potential ecological risks, and historical fluxes of trace elements (Pb, As, and Hg) were evaluated from 210Pb-dated sediment cores in three different areas with gold mining impacts in northern Colombia: the Atrato River (AR), the Delicias Marsh (DM) and the Encaramada Marsh (EM). All cores spanned ∼100 years; the mass accumulation rates followed the order AR > DM > EM. The average trace elements concentrations in the sediment cores were: Pb 2.41 ± 0.72, As 0.65 ± 0.32, Hg 0.07 ± 0.02 μg g−1 in the Atrato River; Pb 23.49 ± 2.59, As 2.46 ± 0.88, Hg 0.10 ± 0.02 μg g−1 in the Delicias Marsh; and Pb 9.76 ± 4.18, As 2.44 ± 1.26, Hg 0.17 ± 0.06 μg g−1 in the Encaramada Marsh. Sediments are classified according to the contamination factor (CF) and geoaccumulation index (Igeo) as low to very highly contaminated. The Pollution load index (PLI) indicates environmental deterioration (PLI> 1), and the Sediment quality guidelines (SQGs) indicate that only Hg may produce adverse biological effects in the EM core. This study is an example of the reconstruction of temporal changes in pollution levels and impacts of potentially toxic elements caused by gold mining in remote ecosystems, which can be reproduced in other areas where environmental monitoring is scarce or non-existent. [Display omitted] • As, Pb and Hg level of contamination and historical fluxes were investigated in three different areas with gold mining impacts in northern Colombia. • All cores spanned ∼100 years, with trace elements showing upward trends to present. • Several contamination indexes shown a strong pollution by As, Pb and Hg in sediments. [ABSTRACT FROM AUTHOR]

Kaohsiung Ocean Dredged Material Disposal Site (KODMDS) that located in the southwest offshore of Taiwan, has been annually disposed about 500,000 ton dredged sediments of Kaohsiung Harbor from 2003 to 2012. Five sediment cores collected from KODMDS and three from nearby reference sites were analyzed to evaluate their sedimentation rates, vertical profiles of heavy metal, and heavy metal pollution indices to assess the impact of dumping harbor dredged sediments into the ocean on the sediment quality in KODMDS. The sedimentation rate of 0.24 cm/y was estimated by the 210 Pb method, which means that the effected depth of the top layer of a core of D1 was affected in the period of dumping dredging sediments. The vertical distribution of heavy metals in the sediment cores from KODMDS showed the concentrations of most heavy metals were slightly elevated in the top layers of the sediment cores, which may be affected by the dumping of harbor dredged sediments. According to the analyzed results of the heavy metal pollution indices, the level of heavy metal pollution, the potential eco-toxicity and the potential ecological risk of the sediments in KODMDS exhibited only a slight increase, which indicated that the increase in concentration of heavy metals may potentially pose the insignificant impact on benthos inhabiting the disposal site. [ABSTRACT FROM AUTHOR]

The Southern Yellow Sea (SYS) is an important reservoir of anthropogenic organic contaminants, such as polybrominated diphenyl ethers (PBDEs). To reconstruct the historical records of PBDEs and examine their relationships with the human activities and organic matters, a 210 Pb-dated sediment core was collected from the central mud area in the SYS. The concentrations of tri-to hepta-BDEs (∑ 7 PBDEs) and BDE-209 ranged from 9.8 to 99.8 pg g −1 d.w. and from 12.1 to 855.4 pg g −1 d.w., respectively, both displaying the increasing trends from the bottom to the surface. More importantly, there was a faster increase for PBDEs since the 1990s, especially for BDE-209, which responded well with the rapid economic growth, and the increases of urbanization and industrialization in the local areas of the SYS. The analogously vertical patterns and significant relationships between PBDEs and total organic carbon (TOC) implied the TOC-dependent deposition of PBDEs in the core. Furthermore, multiple biomarker-based proxies of terrestrial organic matter (TOM) and marine organic matter (MOM) were introduced to systematically investigate the different effects of TOM and MOM on PBDE deposition in the SYS. The similarly down-core profiles and significant correlations were found between PBDEs and the MOM proxies (sum of rassicasterol, dinosterol and C 37 alkenones (∑A + B + D) and marine TOC) as well as the branched and isoprenoid tetraether (BIT), but not for TOM proxies (∑C 27 +C 29 +C 31 n -alkanes, terrestrial and marine biomarker ratio (TMBR) and terrestrial TOC), indicating that MOM was an important factor driving PBDE deposition in the sediment core from the SYS. [ABSTRACT FROM AUTHOR]

The Palos Verdes Shelf (PVS) and the continental slope off the Palos Verdes Peninsula are highly contaminated by degradation products of the pesticide DDT (1-chloro-4-[2,2,2-trichloro-1-(4-chlorophenyl)ethyl]benzene). Sediment samples from two box cores were analyzed to obtain further information about the fate of DDT and its degradation products within the environment. After solvent extraction, an alkaline hydrolysis procedure was applied. A comprehensive screening for 26 DDT compounds revealed that DDT and its degradates contaminate not only the extractable fraction but also the fraction released by alkaline hydrolysis. A comparison of the quantitative distribution of DDT degradation products in the extractable fraction and released by alkaline hydrolysis showed a distinct difference. DDE (1-chloro-4-[2,2-dichloro-1-(4-chlorophenyl)ethenyl]benzene), DDD (1-chloro-4-[2,2-dichloro-1-(4-chlorophenyl)ethyl]benzene), DDMS (1-chloro-4-[2-chloro-1-(4-chlorophenyl)ethyl]benzene), and DDMU (1-chloro-4-[2-chloro-1-(4-chlorophenyl)ethenyl]benzene) were predominant in the sediment extracts but minor components of the hydrolyzable fraction. The most abundant compounds released by the alkaline hydrolysis were DBP (bis(4-chlorophenyl)methanone), DDNU (1-chloro-4-[1-(4-chlorophenyl)ethenyl]benzene), DDM (1-chloro-4-[(4-chlorophenyl)methyl]benzene) and the water-soluble DDA (2,2-bis(4-chlorophenyl)acetic acid). The release of DDA may point to the presence of an important degradation pathway in marine environments. Concentration levels of DDT-related compounds showed corresponding vertical profiles in both fractions, but were significantly lower in the fraction released by alkaline hydrolysis. In contrast to fluvial sediments contaminated by DDT and its degradates the alkaline hydrolysis products represented a minor portion of the total sedimentary burden in the analyzed marine sediments. These findings show the necessity of a comprehensive screening for all DDT isomers and breakdown products in the extractable and non-extractable fraction to assess the total contamination abundance and potential environmental risks. [ABSTRACT FROM AUTHOR]

Legacy and alternative halogenated flame retardants (HFRs), such as polybrominated diphenyl ethers (PBDEs), novel brominated flame retardants (NBFRs), and dechlorane plus (DP), were measured in dated sediments from a highly industrialized lake in Korea. All HFRs were detected in almost all of the sediment depth layers for more than 70 years, indicating a history of long-term contamination. Similar historical trends in PBDEs, 1,2-bis(2,4,6-tribromophenoxy)ethane (BTBPE), and DP were observed in dated sediments, whereas decabromodiphenylethane (DBDPE), and 2-ethylhexyl-2,3,4,5-octabromo-1,3,3-trimethyl-1-phenylindane (OBIND) concentrations sharply increased since the 1990s. Moreover, the concentration ratios of DBDPE/BDE 209 increased from the early 1990s to the present. Our findings suggest that DBDPE and OBIND have been used as HFR alternatives. The historical record of the concentrations and profiles of legacy and alternative HFRs corresponded with industrial activities, consumption of FRs, and coastal development activities. Inventories of legacy and alternative HFRs were similar to those reported for highly industrialized regions around the globe. [Display omitted] • Legacy and alternative HFRs were detected in an industrialized lake for a period >70 years. • BTBPE and DP were historically consumed along with PBDEs. • DBDPE and OBIND levels increased since the regulations on PBDEs in dated sediment. • Increasing ratios of DBDPE/BDE 209 over time indicate a shift in HFR consumption patterns. • Historical trends in HFRs were influenced by industrial and coastal development activities. [ABSTRACT FROM AUTHOR]

Highlights: [•] Chronological records of metal deposition at different estuarine sites were studied. [•] Sedimentary metal speciation reveal responses to upstream hydrological events. [•] The transformation of metal speciation can explain the intercepting role of dams. [•] Sediment particles and organic carbon are the proxies for the metals deposition. [Copyright &y& Elsevier]

Highlights: [•] Sediment cores were collected from reservoir sediments of the Pearl River Delta. [•] Cu, Zn, Ag, Cd, and As were significantly accumulated during last three decades. [•] Heavy metals were strongly associated with algal organic matter in the sediments. [•] Principal component analysis was used to assess the enrichment of heavy metals. [•] Sedimentary process of heavy metals was affected by primary productivity. [ABSTRACT FROM AUTHOR]

Highlights: [•] Sediment cores from five critical regions in the Tibetan Plateau were analysed for OCPs. [•] The recent increasing trends of OCPs are likely due to the greatest retreat of glaciers. [•] The recycling of OCPs in the plateau cryosphere is more sensitive monitor of climate warming. [Copyright &y& Elsevier]

Abstract: In the present study, hexabromocyclododecanes (HBCDs) were investigated in the sediment from Haihe River (HR), Dagu Dainage Canal (DDC) and Tianjin Harbor (TH) at Bohai Bay using a total of 51 samples of surface sediments and a sediment core collected from May to September in 2010, and its diastereomer- and enantiomer-specific profiles were analyzed. The concentration of total HBCDs were generally high, with mean value and ranges of 31.0 and 1.35–634ngg−1 dw, respectively. The contamination followed the order of TH>DDC>HR. Higher levels (up to 634ngg−1 dw) occurred in the lower reach of HR and DDC located in an industrial area of Tianjin. This is the first time to report so high concentration of HBCDs in sediment in Southeast Asia. The γ-diastereomer dominated in most samples (44 out of 51), and this is in agreement with the diastereomer distribution pattern in industrial products, while α-HBCD was the dominant diastereomer in the other seven samples. However, only few samples exhibited γ-diastereomer ratio similar to that (75–89%) in technical products, indicating the inter-transformation and variable degradation of the different isomers. The high ratio of γ-diastereomer could be used as an indicator for fresh contamination input. Enantiomeric factors (EFs) of HBCD isomers in most of the samples were statistically different from technical products (p <0.05), showing a trend of more easily enrichment of the (−)-HBCD-enantiomer compared to the (+)-HBCD-enantiomer. The δ- and ε-diastereomers were frequently detected but at low level. The HBCDs in the sediment core showed several peaks, and the greatest value occurred in 2005, when a plastic manufacture plant using HBCD was set up nearby. [Copyright &y& Elsevier]

Abstract: Concentrations of polycyclic aromatic hydrocarbons (PAHs) were detected in sediment cores and surface sediment samples from the Liangtan River of Chongqing, Southwest China. The total concentration of 16 PAHs ranged from 69 to 6251ngg−1. The spatial distribution of the PAHs reflects the intensity and scope of human activity in the catchment. A historical record of PAH contamination was reconstructed using a sediment core from a background segment of the river. The characteristic changes of concentrations, fluxes and patterns of 16 PAHs over the past ∼90years were captured in detail. An obvious peak of PAH concentration and flux was found in the 1940s, i.e., during war time, and then a sharp increase was observed from the early 1980s to the present. The maximum concentration and flux reached 1260ngg−1 and 470ngcm−2 year−1, respectively. The sharp increase was attributed to the contribution of pyrogenic sources of PAHs. The population, length of highways and energy consumption of Chongqing, as indexes of socioeconomic development, were positively correlated with PAH input in the sediment core from the 1950s to the present. The results clearly show that the local socioeconomic development in the last decades remarkably aggravated the environmental load of sedimentary PAHs. [Copyright &y& Elsevier]

Abstract: In the present study, a depth-related distribution of Persistent Organic Pollutants (POPs) in sediments of Lake Iseo, one of the major southern Alpine Italian lakes, is reported in order to further test the hypothesis of melting Alpine glaciers as a secondary source of contamination. In a previous paper, a “glacier contamination hypothesis” was suggested to explain the unexpected contamination of the biota of Lake Iseo, mainly fed by the Alpine melting ice. The sediment core analyses covered around the last 50years. The organic matter profile evaluated as a Loss-On-Ignition percentage indicated transition of the basin from an oligotrophic to a mesotrophic status at around the early 1970s, but there was no evidence of the shift to eutrophy in the 1980s. Among DDTs, pp’DDE was the predominant metabolite, accounting on average for 79.4% of the total DDT concentrations and ranging from 6.4 to 447.5ngg−1 d.w. PCBs ranged from 5.0 to 163.7ngg−1 d.w. The maximum PCB concentrations were found in sediment layers corresponding to the 1970s when the highest production and use of these compounds occurred in Italy. In contrast, concentrations of DDTs showed a sharp increase from the early 1990s, long after their agricultural use was banned in Italy. This delayed pollution provides support for the hypothesis that the recent retreat of glaciers represents a secondary pollution source for old pesticides that were stored in the ice at the time of their use in agriculture. [Copyright &y& Elsevier]

Dated sediment cores provide an excellent way to investigate the historical input of persistent organic pollutants into the environment and to identify possible sources of pollution. The vertical distribution of polychlorinated dibenzo-p-dioxins/polychlorinated dibenzofurans (PCDD/F) and polychlorinated biphenlys (PCB) was investigated in a sediment core from Greifensee to elucidate the historical trends of PCDD/F and PCB inputs between 1848 and 1999. Concentrations of PCB and PCDD/F increased by more than one order of magnitude between 1930 and 1960. PCB and PCDD/F concentrations were 5700ng/kg dry weight (dw) and 160ng/kg dw, respectively, in sediments originating from the late 1930s and reached a maximum of 130000ng/kg dw and 2400ng/kg dw, respectively, in the early 1960s. From 1960 on, concentrations decreased to the 1930s level by the mid 1980s. A remarkable shift in the PCDD/F pattern was observed after the early 1940s. Before 1940, the PCDD/F pattern was PCDF dominated (ratio of PCDD to PCDF=0.41±0.11), while the PCDD started to be the major species after the early 1940s (ratio of PCDD to PCDF=1.46±0.38). The temporal trends of PCB and PCDD/F correlate surprisingly well with each other. This might be due to the coincidence of two factors. The introduction of PCB on the market in the 1930s resulted in emissions due to the widespread use of these industrial chemicals. In the same time period, waste incineration became an increasingly popular way to get rid of garbage, boosting the PCDD/F emissions significantly. The rapid decline of PCDD/F and PCB concentrations in the sediment starting in the early 1960s reflects the result of better emission control techniques in thermal processes and the improvement of waste water treatment in the catchment of Greifensee. [Copyright &y& Elsevier]

Brominated flame retardants (BFRs) are anthropogenic compounds that are ubiquitous in most manufactured goods. Few legacy BFRs have been recognised as persistent organic pollutants (POPs) and have been prohibited since the 2000s. However, most BFRs continue to be used despite growing concerns regarding their toxicity; they are often referred to as novel BFRs (nBFRs). While environmental contamination due to chlorinated POPs has been extensively investigated, the levels and spatiotemporal trends of BFRs are comparatively understudied. This study aims to reconstruct the temporal trends of both legacy and novel BFRs at the scale of a river corridor. To this end, sediment cores were sampled from backwater areas in four reaches along the Rhône River. Age-depth models were established for each of them. Polychlorinated biphenyls (PCBs), legacy BFRs (polybrominated diphenyl ethers - PBDEs, polybrominated biphenyls - PBBs and hexabromocyclododecane - HBCDDs) and seven nBFRs were quantified. Starting from the 1970s, a decreasing contamination trend was observed for PCBs. Temporal trends for legacy BFRs revealed that they reached peak concentrations from the mid-1970s to the mid-2000s, and stable concentrations by the mid-2010s. Additionally, individual concentrations of nBFRs were two to four orders of magnitude lower than those of legacy BFRs. Their temporal trends revealed that they appeared in the environment in the 1970s and 1980s. The concentrations of most of these nBFRs have not decreased in recent years. Thus, there is a need to comprehend the sources, contamination load, repartition in the environment, and toxicity of nBFRs before their concentrations reach hazardous levels. • Time trends of legacy BFRs in sediments along the Rhône River are similar. • Legacy BFRs reached their peak between the 1970s and the 2000s, and are now stable. • nBFRs concentrations are two to four times lower than that of legacy BFRs. • Some nBFRs appeared along the Rhône River as early as the 1970s–1980s. • No decreasing trend in nBFRs concentrations has been observed, so far. [ABSTRACT FROM AUTHOR]

Microplastics are an emerging hazard in the marine environment, and considered to eventually sink into sediments. An investigation into the long-term variation of microplastic accumulation in sediment cores is essential for understanding the historical trend of this contamination and its response to human activities. In this study, the multidecadal changes of microplastic abundances in two sediment cores from the inner shelf of the East China Sea (ECS) were revealed by two methods, i.e., a visual enumeration method based on scanning electron microscopy-energy dispersive X-ray spectroscopy (SEM-EDS) and a quantitative method based on microplastic-derived carbon (MPC) abundances. The features of microplastics were determined via SEM-EDS and micro-Fourier transform infrared spectroscopy (μ-FTIR). The results reveal a multidecadal increasing trend of microplastic accumulation in the coastal sediments of the ECS since the 1960s, which may be jointly governed by the release of plastic wastes and oceanographic dynamics. Meanwhile, the breakpoint of the exponential growth of microplastics in the ECS occurs in 2000 AD, which well matches the rapid increasing of plastic production and consumption in China. Further, based on the MPC contents in sediments, the influence of microplastics on the quantitative evaluation of carbon storage in the ECS has been examined for the first time, revealing an insignificant (<2% before 2014 AD) but potentially-increasing (6.8% by 2025 AD) contribution of microplastics to carbon burial. Our results may provide the important data for evaluating and mitigating the impact of microplastics on the marine environment. Image 1 • A multidecadal increasing trend of microplastic accumulation was revealed in sediment cores in the ECS since the 1960s. • High abundances of microplastics were detected in the form of fragments with the prevalent size of <100 μm. • Microplastic accumulation in sediments in the ECS is associated with Chinese plastic production and consumption. • Microplastics have made an insignificant but potentially-increasing contribution to sedimentary carbon storage in the ECS. [ABSTRACT FROM AUTHOR]

Contamination levels and temporal trends of polybrominated diphenyl ethers (PBDEs) and some alternative brominated flame retardants (BFRs) were examined in a dated sediment core from the deepest part of the Beppu Bay, southwestern Japan. PBDEs were found in the upper layers of 0–15 cm depth at concentrations ranging from 5200 to 32,600 pg g−1 with the peak estimated at 1995. Decabromodiphenyl ether (BDE-209) was the most abundant congener, accounting for 96% in average of total PBDEs. The vertical profile of BDE-209 observed in our sediment core generally agreed with the historical pattern of domestic demand of commercial deca-BDE mixtures in Japan, and perfectly matched with maximum stock of these products (i.e., 42,000 tons in 1995). Among alternative BFRs, only decabromodiphenyl ethane (DBDPE), a replacement of deca-BDE, was found at significant levels with concentrations of 69–850 pg g−1 in sediment layers dated between 1991 and 2011. Ratios of DBDPE to BDE-209 gradually increased during this period, implying opposite trends of these two compounds and the role of DBDPE as a deca-BDE's alternative. The occurrence of deca-BDE components in sediments may pose medium risk to benthic aquatic life, while the ecological risk of other PBDE homologs and DBDPE was negligible. Image 1 • PBDEs and DBDPE were examined in a sediment core from Beppu Bay, Japan. • BDE-209 was the most predominant congener in all the sediment layers. • BDE-209 concentrations peaked at the mid-1990s, then decreased and kept constantly. • DBDPE/BDE-209 ratios gradually increased during 1991–2011. • No serious ecological risk of PBDEs and DBDPE was estimated. [ABSTRACT FROM AUTHOR]

We reconstructed the history of the inputs of hexachlorocyclohexanes (HCHs) and dichlorodiphenyltrichloroethanes (DDTs) into the marine environment to reveal the time-dependent influence of sources and associated anthropogenic activities in China, based on 210Pb-dated cores from the East China marginal seas (ECMS). The temporal dynamics of pesticide contamination expresses as deposition fluxes, inventories, and half-life estimations varied among the cores, suggesting heterogeneity in transport pathways of pollutants. The depth profiles of pesticide inputs closely followed their historical production and application timelines in China, and were also affected by human activities in catchments, with general declines in HCH and DDT inputs to the coring sites after their peak deposition. Despite the prevalence of occurrence of weathered HCH/DDT in the cores, there were clear source-dependent differences in isomeric composition and accumulation between before and after these pesticides were banned. α -HCH and p , p ′-DDT were relatively more enriched in sediments from the pre-ban period when heavy technical HCHs and DDTs use occurred, as indicated by the higher α -/ β -HCH and lower (DDE + DDD)/DDTs ratios, and the larger fractions of α -HCH and p , p ′-DDT influxes to the coring sites in the ΣHCH and ΣDDT fluxes, respectively, while this pattern shifted to be historical residue-based in the post-ban period. The difference in the recent influxes of pesticides to core sediments and their higher post-ban inventories highlight the increasing importance of historical sources over time and continuous input of weathered residues into marine environment via lateral transport. Image 1 • Dynamics of deposited HCHs and DDTs in the ECMS were related to input pathways. • Compositions and accumulations of pesticides varied with time-dependent sources. • Weathered HCHs and DDTs dominated their current inputs to the ECMS. • Importance of lateral transport of residual pesticides into the ECMS is rising. [ABSTRACT FROM AUTHOR]

The atmospheric deposition of polycyclic aromatic compounds (PACs) is considered a major pathway to isolated lakes and bogs in the Athabasca oil sands region (AOSR), Canada. However, the suite of PACs measured has been limited. We report the detailed depositional history of nitrogen and sulphur heterocyclic PACs using a 210Pb dated sediment core (1914–2015) near major developments in the AOSR. We observed (1) an exponential growth in the deposition of heterocyclic PACs to recent times with an average doubling time of 12 years, (2) significant breakpoints in PAC fluxes in the mid to late 1980s, and (3) a synchronous increase of PACs with crude oil production (r2 = 0.82, p = 0.001). NPACs were not detected prior to the 1960s in the sediment core studied, suggesting they may hold promise in serving as indicators for atmospheric PAC deposition of industrial origin. Furthermore, a change in heterocyclic PAC distribution profiles beginning in the 1970–1980s, after the onset of mining, resembling a petcoke signature, was also observed. Significant positive correlations (p < 0.05) were observed between heterocyclic PACs, and several metal(loid)s, including priority pollutant elements, chromium and beryllium, and rare earth elements, cerium, lanthanum and yttrium (r2 > 0.75), suggesting the potential of a common source or similar transport and fate mechanisms. Significant negative or no correlations were observed between heterocyclic PACs and other metal(loid)s, including vanadium, total mercury and lead, possibly reflecting the impact of broader regulatory controls introduced in the mid-1970s on some metal(loids) but not on PACs, including the installation of electrostatic precipitators in major upgrader stacks. Image 1 • Sulphur polycyclic aromatic compounds (PACs) were more abundant than nitrogen PACs. • Sulphur PACs detected since 1930s, while nitrogen PACs not detected before 1960s. • Heterocyclic PACs doubling time of 12 yrs, while routine PACs was between 18 and 25 yrs. • Heterocyclic PAC distribution profiles change began in 1970s post oil sands onset. [ABSTRACT FROM AUTHOR]

Coral reefs are challenged by multiple stressors due to the growing industrialization. Despite that, data on their environment are still scarce, and no research is yet performed on polybrominated diphenyl ethers in the Persian Gulf area. Seeking to fill in this gap, the present study aims to determine spatio-vertical distributions, source apportionment and ecological risk of polybrominated diphenyl ethers in the sediment cores and seawater samples from ten coral reef Islands in the Persian Gulf, Iran. Σ 12 PBDEs concentrations ranged from 0.42 ± 0.04 to 47.14 ± 1.35 ng g−1 dw in sediments, and from 1.17 ± 0.06 to 7.21 ± 1.13 ng L−1 in seawater. The vertical polybrominated diphenyl ethers distribution varied significantly among the sampling stations and different depths with a decreasing trend towards the surface and peaks around 12–20 cm. Both in the seawater and sediment samples, elevated polybrominated diphenyl ethers loadings were observed in highly industrialized areas. Deca-bromodiphenyl ether-209 was the predominant congener along the sediment cores, whereas Tetra-bromodiphenyl ether-47 and Penta-bromodiphenyl ether-100 dominated in seawater samples. Commercial Deca-bromodiphenyl ether mixture was found to be the major source of polybrominated diphenyl ethers. Penta-bromodiphenyl ether was revealed to be the major ecological risk driver in the study area: it posed medium to high-risk quotient to sediment dwelling organisms. This study indicated that coral reefs are playing an important role in retaining polybrominated diphenyl ethers and highlighted the need to manage polybrominated diphenyl ethers contamination in the coral reef environment. Image 1 • PBDE contamination in Iranian coral reefs is reported for the first time. • The highest ∑PBDE loadings were observed in highly industrialized areas. • BDE-209 prevailed in sediment cores, BDE-47 and BDE-100 dominated in water samples. • Penta-BDE is the main ecological risk driver in the study area. [ABSTRACT FROM AUTHOR]