Depuration Rate Research Articles

Prediction of Depuration Rate Constants for Polychlorinated Biphenyl Congeners.

The integral equation formalism polarizable continuum model (IEF-PCM) for solvent effects with the default solvent (water) and solvent parameters, together with the density functional theory method at 6-31G(d) level, was used to optimize molecular structures for polychlorinated biphenyl (PCB) congeners. Four molecular descriptors were selected to develop quantitative structure–activity relationship (QSAR) models for the depuration rate constants (kd) of 63 PCB congeners in a juvenile rainbow trout (Oncorhynchus mykiss). The optimal multiple linear regression (MLR) model has the correlation coefficient R of 0.933 and the root mean square (rms) error of 0.0681 for the total set of 63 PCB congeners. The support vector regression model has R of 0.953 and rms error of 0.0576 for the total set. Both the MLR and SVM QSAR models in this paper were accurate and acceptable compared with other QSAR models for the depuration rate of PCB congeners reported in references. Thus, applying IEF-PCM and B3LYP/6-31G(d) calculations for molecular descriptor derivation of PCB congeners is successful.

Bioconcentration, depuration and toxicity of Pb in the presence of titanium dioxide nanoparticles in zebrafish larvae

The interactions between nanoparticles (NPs) and metals in aquatic environments may modify the bioavailability and toxicity of metals to organisms. In this study, we investigated the effects of titanium dioxide NPs (n-TiO2) on the bioconcentration, depuration, and neurotoxic effects of lead (Pb) in zebrafish larvae. Transmission electron microscopy coupled with energy-dispersive X-ray spectroscopy showed that Pb2+ was adsorbed by n-TiO2 to form NP–Pb complexes in suspension, and these complexes were observed in larval tissues. The bioconcentration of Pb in larvae along with the depuration rates of Pb were higher in the presence of n-TiO2 compared to when n-TiO2 was absent. Exposure to Pb alone induced the expression of the biomarker metallothionein, downregulated neurodevelopment-related genes, and reduced swimming activity of larvae. However, the addition of n-TiO2 to the exposure solution alleviated these effects. The results suggest that n-TiO2 can act as a carrier of Pb to increase its bioconcentration; however, the formation of NP–Pb complexes likely reduces the amount of free Pb2+, thereby reducing toxicity to larvae.

Glutathione biosynthesis plays an important role in microcystin-LR depuration in lettuce and spinach

Irrigation of crop plants with microcystins (MCs) contaminated water could be a threat to human health via bioaccumulation. Despite the fact MCs bioaccumulation in crop plants is well documented, MCs depuration, as well as the mechanism involved remains unclear. The objectives of the present study were to investigate the bioaccumulation and depuration of microcystin-LR (MC-LR) in lettuce (Lactuca sativa L.) and spinach (Spinacia oleracea L.), as well as to explore the role of glutathione (GSH) biosynthesis in MC-LR depuration. The tested plants were irrigated with deionized water containing 10 μg L−1 MC-LR for 12 days (bioaccumulation), and subsequently, with either deionized water only or deionized water containing 0.5 mM buthionine sulfoximine (BSO, a specific inhibitor of GSH biosynthesis) for 12 days (depuration). After bioaccumulation period, highest concentrations of MC-LR found in lettuce and spinach were 114.4 and 138.5 μg kg−1 dry weight (DW) respectively. Depuration rates of MC-LR in lettuce and spinach were 9.5 and 8.1 μg kg−1 DW d−1, which deceased to 3.7 and 4.6 μg kg−1 DW d−1 in treatments with BSO application. GSH content in both lettuce and spinach were not significantly affected during depuration without BSO; whereas after treatment with BSO, GSH content significantly decreased by 36.0% and 24.7% in lettuce and spinach on 15 d, and the decrease remained on 18 d and 21 d in lettuce. Moreover, during the bioaccumulation period, activities of glutathione reductase (GR) and glutathione S-transferase (GST) were enhanced in both plants. Our results suggested that GSH biosynthesis played an important role in MC-LR depuration in the tested plants. Concerning human health risk, most of the estimated daily intake (EDI) values during the bioaccumulation period exceeded the tolerable daily intake (TDI) guideline. However, the risk could be alleviated by irrigating with MCs-free water for a certain amount of time before harvest.

Impact of co-exposure to titanium dioxide nanoparticles and Pb on zebrafish embryos

Complex interactions have been established between nanoparticles (NPs) and heavy metals in real environments. Herein we used zebrafish embryos to investigate the influence of titanium dioxide NPs (n-TiO2) on the uptake, bioconcentration, and depuration, and toxicity of Pb. The formation of n-TiO2–Pb complexes was confirmed in an exposure suspension. An increase in Pb bioconcentration was observed in zebrafish embryos upon co-exposure to n-TiO2 and Pb; moreover, n-TiO2–Pb complexes could be found in the embryos, indicating the bioavailability of NPs. However, there was no difference in the depuration rates of Pb in the presence of n-TiO2. Metallothionein (MT) content was significantly increased upon exposure to Pb alone, and the content significantly increased even further upon co-exposure. A downregulation in the expression levels of the neurodevelopment-related genes gfap, syn2α, and elavl3 was observed in the embryos, and we also noted a reduction in the swimming speed of and the total distance traveled by the larvae. To summarize, our results indicate that n-TiO2 can act as an effective carrier of Pb to enhance its uptake, bioavailability, and toxicity in zebrafish embryos.

Uptake and depuration of eight fluoroquinolones (FQs) in common carp (Cyprinus carpio)

Fluoroquinolones (FQs) are extensively used in humans and animals, which have aroused wide attention due to the emergence of FQ resistant bacteria and frequent detection in water, sediment and organism. However, little information is available about the bioconcentration and tissue distribution of FQs in fish. In the present study, we investigated the uptake and depuration of eight FQs (balofloxacin (BAL), enoxacin (ENO), enrofloxacin (ENR), fleroxacin (FLE), lomefloxacin (LOM), moxifloxacin (MOX), ofloxacin (OFL), sparfloxacin (SPA)) in common carp under controlled laboratory conditions. The results showed that all target FQs could accumulate in fish tissues, and had a similar tendency over time during the whole uptake and depuration periods. The uptake rate constant (k1), depuration rate constant (k2) and half-lives (t1/2) were in the ranges of 0.007–3.599 L/(kg·d), 0.051–0.283 d−1 and 2.4–10.7 d, respectively. The ranges of bioconcentration factors (BCFs) were 0.24–39.55 L/kg, 0.21–24.97 L/kg and 0.04–1.07 L/kg in liver, kidney and muscle, respectively. BCFs of eight FQs decreased in the order: MOX > ENR > ENO ≈ BAL ≈ FLE ≈ OFL ≈ LOM ≈ SPA, which may be correlated with the substituents at positions 7 and 8 of the basic quinolone nucleus and the metabolic capacity. Besides, BCFs were relative with pH-adjusted distribution coefficient (log D), suggesting that molecular status of ionizable compounds strongly influenced the bioconcentration processes. The present study provides important insights for understanding the bioconcentration and tissues distribution of FQs.

Spatial variability and depuration of tetrodotoxin in the bivalve Paphies australis from New Zealand.

Tetrodotoxin (TTX) is a potent neurotoxin responsible for many human intoxications globally. Despite its potency and widespread occurrence in taxonomically diverse species, the primary source of TTX remains uncertain. Paphies australis, an endemic clam found in New Zealand, has been found to contain TTX in several locations. However, it is unknown if this represents endogenous production or accumulation from an external source. To address this question, the concentrations of TTX in whole P. australis and dissected organs (siphons, foot, digestive gland and the ‘rest’) from thirteen sites around New Zealand were determined using liquid chromatography-tandem quadrupole mass spectrometry analysis (LC-MS/MS). Depuration rate of TTX was also investigated by harvesting and measuring concentrations in P. australis maintained in captivity on a toxin-free diet every three to 15 days for 150 days. The LC-MS/MS analyses of the spatial samples showed that TTX was present in P. australis from all regions tested, with significantly (p < 0.001) higher concentrations (15–50 μg kg−1) observed at lower latitudes of the North Island compared with trace levels (0.5–3 μg kg−1) in the South Island of New Zealand. Tetrodotoxin was detected in all the dissected organs but the siphons contained the highest concentrations of TTX at all sites analysed. A linear model of the depuration data identified a significant (p < 0.001) decline in total TTX concentrations in P. australis over the study period. The siphons maintained the highest amount of TTX across the entire depuration study. The digestive glands contained low concentrations at the start of the experiment, but this depurated rapidly and only traces remained after 21 days. These results provide evidence to suggest that P. australis does not produce TTX endogenously but obtains the neurotoxin from an exogenous source (e.g., diet) with the source more prevalent in warmer northern waters. The association of higher TTX concentrations in shellfish with warmer environments raises concerns that this toxin's distribution and abundance could become an increasing human health issue with global warming.

A simulation of the seasonal variation of decabromodiphenyl ether in a bay adjacent to the Yellow Sea

A three-dimensional transport-ecosystem-POP coupled model is configured to simulate the seasonal variation and budget of decabromodiphenyl ether (BDE-209) in a semi-enclosed bay adjacent to the Yellow Sea. The model includes five types of BDE-209 (gaseous, dissolved, phytoplankton-bound, detritus-bound, and suspended particulate matter (SPM)-bound) and related physical and biogeochemical processes, such as advection and diffusion due to seawater motion, input from rivers, air-sea exchange, decomposition of dissolved BDE-209, uptake and depuration between dissolved and phytoplankton-bound BDE-209, mortality of phytoplankton-bound BDE-209, remineralization and sinking of detritus-bound BDE-209, and sinking of SPM-bound BDE-209. Model results show that the dissolved and particulate BDE-209 in the bay are higher in the nearshore area than in offshore area and are higher in summer than in other seasons; these results are consistent with field data. SPM-bound BDE-209 is dominant among the five types due to its large supplying from rivers. Dissolved BDE-209 concentrations are around 5-fold that of phytoplankton-bound BDE-209, which depends on uptake and depuration rate constants between dissolved and phytoplankton-bound BDE-209 and biomass of phytoplankton. Evaluation of mass balance indicates that the input from rivers is major source of BDE-209, while the exchange with the Yellow Sea is major sink. Sensitivity experiments demonstrate that the input of BDE-209 from rivers plays the most significant role in the seasonal variation of dissolved and particulate BDE-209 concentrations, and the change in water temperature is a secondary factor.

Ecotoxicity screening of novel phosphorus adsorbents used for lake restoration

Short-term standardized laboratory tests were carried out for evaluating acute and chronic toxicological effects of novel phosphorus (P) adsorbents on Raphidocelis subcapitata (algal growth rate inhibition) and on Daphnia magna (immobilization, with direct and indirect exposure to adsorbents, and uptake-depuration tests). Four P adsorbents were tested: two magnetic (HQ and Fe3O4) and two non magnetic (CFH-12® and Phoslock®). For the case of the algal growth inhibition test, the EC50 was 1.5 and 0.42 g L−1 for HQ and CFH-12®, respectively, and no inhibition patterns were observed neither for Fe3O4 nor for Phoslock®. When organisms were exposed to a direct contact, in the D. magna immobilization test, no statistically significant differences were found in the EC50 values among the four studied adsorbents. The huge difference between direct and indirect contact experiments suggests that toxicity is mainly physically mediated. The uptake-depuration test evidenced a much faster uptake and depuration rates for Phoslock®, which was precisely the adsorbent with the highest particle size. In a realistic worst-case scenario using data from Honda lake (Almería, Spain), where lake restoration is carried out by a adding a single large dose to bind surplus P in the lake, the predicted environmental concentrations for all adsorbents were lower than EC50 for all adsorbents and they were found to exceed a provisional limit value for ecotoxicity after a short-term exposure. All in all, since neither accumulation nor longer term effects of P adsorbents in the pelagic phase is expected, this risk may however, on a case-to-case basis, be acceptable.

Bioaccumulation of selected veterinary medicinal products (VMPs) in the blue mussel (Mytilus edulis)

Veterinary medicinal products (VMPs) are widely used within the fish farming industry to control sea lice infestations. There is concern that wild and farmed mussels in the vicinity to these fish farms may be exposed and subsequently bioaccumulate these chemicals, which could pose a threat to human health. To understand the fate of these chemicals in the environment, controlled laboratory exposures were performed to establish the uptake and depuration of selected VMPs in the blue mussel (Mytilus edulis). The VMPs included teflubenzuron, emamectin benzoate and deltamethrin. The effects of salinity on the bioaccumulation of teflubenzuron were also investigated to see whether mussels in brackish waters exhibit different bioaccumulation dynamics. Salinity had no significant effect on the uptake or depuration curves for teflubenzuron down to 15‰. The uptake rate constants (k1) for teflubenzuron, emamectin benzoate and deltamethrin in mussels were 192, 4.82 and 2003, with kinetic bioconcentration factors (BCFs) of 1304, 49 and 2516. Depuration rate constants (k2) were also found to differ between the three VMPs at 0.147, 0.048 and 0.796 for teflubenzuron, emamectin benzoate and deltamethrin, with calculated elimination half-lives (t1/2)of 4.7, 14 and 0.87 days. The longer elimination half-lives for teflubenzuron and emamectin benzoate, suggest that these chemicals accumulate in blue mussels and therefore have the potential to bioaccumulate in wild and farmed mussel populations in the environment.

Bioaccumulation and acute toxicity of As(III) and As(V) in Nile tilapia (Oreochromis niloticus)

The distribution of arsenic in the different tissues of tilapia fish is determined by the exposure time and the depuration rate. The mechanisms of toxicity/carcinogenicity depend on the arsenic species involved in the biotransformation processes. After a 7-day exposure period, the accumulation of inorganic arsenic (iAs) in the tilapia tissues studied was in the order: liver > stomach > gills > muscles. In bioaccumulation assays, the values of the organ uptake constant (ka) ranged from 0.06 to 0.51 mL g−1 d−1, while the depuration rate constant (kd) values were in the range 0.03–1.15 d−1. Higher iAs bioaccumulation factor (BCF) values were observed for the stomach (3.1 mL g−1) and the liver (1.6 mL g−1), reflecting their high capacity to accumulate iAs species. These organs act as long-term storage sites for iAs, following chronic exposure. The LC50 values were determined considering the average iAs concentration and the cumulative fish mortality. For As(III), the LC50 values indicated fish mortality at concentrations above 30 mg L−1. The fish showed greater tolerance to exposure to As(V), compared to As(III), with fish mortality after the second day of exposure requiring an As(V) concentration 7-fold higher than As(III).

Transformation and Depuration of Paralytic Shellfish Toxins in the Geoduck Clam Panopea globosa From the Northern Gulf of California

In January 2015 a harmful algae bloom (HAB) of the dinoflagellate Gymnodinium catenatum occurred in the Northern Gulf of California (NGC). This species produces paralytic shellfish toxins (PSTs) a group of potent neurotoxins. The harvesting and commercialization of geoduck Panopea globosa are important economic activities in this region. These activities were prohibited for several months due to the accumulation of PSTs in clam tissues. We analyzed PSTs concentrations in P. globosa collected on a weekly basis during 2015 near San Felipe, Baja California. The goal of the study was to evaluate the transformation and depuration characteristics of PSTs in the geoduck tissues. Three organisms from each sampling date were dissected and the PST content was evaluated in the visceral mass and siphon by high performance liquid chromatography with post column oxidation (HPLC-PCOX). Ten selected samples were also analyzed by hydrophilic interaction chromatography coupled to tandem mass spectrometry (HILIC-MS/MS). Toxicity in the siphon was lower than 800 µg STX eq kg-1 (the regulatory limit for PSTs) in all samples. In contrast, the maximum toxicity in the visceral mass exceeded 21 times this limit. It took 210 days to reach the regulatory limit after a maximum toxicity of 16,740 µg STXeq kg-1 was detected. Therefore, P. globosa is a slow detoxifier bivalve with a depuration rate of 4.26 day-1 (adjusted to an exponential decay model; r2=0.80). C1&2 were the most abundant analogues in siphon and viscera samples collected close to the HAB occurrence. The concentration of these analogues decreased and more toxic analogues as GTX5, dcGTX2 and dcSTX were detected. M-type analogs were detected by HILIC-MS/MS and represented up to 75% of total PSTs in some samples. M-type analogs contributed to 48% of toxicity estimated in the sample. We report for the first time the depuration rate, PSTs profile and its change over time in P. globlosa. This information is essential to characterize the metabolism of toxins in this economically important bivalve but also to develop management plans for the fishery if the organism is going to be recurrently exposed to PSTs producing blooms, as seems the case for the NGC.

Characterizing the Influence of Metabolism on the Halogenated Organic Contaminant Biomagnification in Two Artificial Food Chains Using Compound- and Enantiomer-Specific Stable Carbon Isotope Analysis.

Two artificial food chains, food tiger barb-oscar fish and food tiger barb-redtail catfish, were established in the laboratory. The species-specific biotransformation of ortho, para'-dichlorodiphenyltrichloroethane, 12 polychlorinated biphenyl, and five polybrominated diphenyl ether congeners were characterized by measuring the compound- and enantiomer-specific stable carbon isotope composition (δ13C), enantiomeric fraction of the chiral chemicals, and metabolites in the fish. Compound- and enantiomer-specific biotransformations were revealed by the alteration of δ13C and EF in both predator fish species. Significant correlations between the carbon stable isotope signatures and the depuration rates and biomagnification factors (BMF) were observed. Chemicals that exhibited changes in δ13C during the experiment have higher kd and lower BMF values than those with unchanged δ13C. Specifically, the difference between the predicted BMF based on the log Kow and the measured BMF, ΔBMF, was significantly positively and linearly correlated to the change in the δ13C (expressed by Δδ13C/δ13Cinitial, the percentage of Δδ13C: δ13Cending-δ13Cinitial to the initial δ13Cinitial) in both food chains. These results indicated that the impact of metabolism on the bioaccumulation potential of organic contaminants can be predicted by the stable carbon isotope fractionation of chemicals in the fish.

Similarities and differences of 137Cs distributions in the marine environments of the Baltic and Black seas and off the Fukushima Dai-ichi nuclear power plant in model assessments

The compartment model POSEIDON-R with an embedded food web model was used to assess 137Cs distributions in the Baltic and Black seas and off the Pacific coast of Japan during 1945–2020 due to the weapon testing and accidents at the Chernobyl and Fukushima Dai-ichi nuclear power plants. The results of simulations conducted with generic parameters agreed well with measurements of 137Cs concentrations in the water, bottom sediments, and in fish. In the Black and Baltic seas, salinity variations affected the transfer of 137Cs through the food web. The contamination of pelagic fish followed the water contamination with some delay, whereas demersal fish depuration was found to be related to decreasing 137Cs concentrations in the upper sediment layer. On the Pacific shelf off Japan, intensive currents and eddies caused the simulated depuration rates in fish to be one-two orders of magnitude larger than those in the semi-enclosed Black and Baltic seas.

Effects of ocean acidification on 109Cd, 57Co, and 134Cs bioconcentration by the European oyster (Ostrea edulis): Biokinetics and tissue-to-subcellular partitioning

The uptake and depuration kinetics of dissolved 109Cd, 57Co and 134Cs were determined experimentally in the European flat oyster Ostrea edulis (Linnaeus, 1758) under different pH conditions (i.e., 8.1, 7.8 and 7.5) for 59 days. Uptake and depuration rates were variable within these elements; no effects were observed under different pH conditions for the uptake biokinetics of 109Cd and 57Co and depuration of 109Cd and 134Cs in oyster. The uptake and depuration rate constants of 134Cs differed during the exposure phase between treatments, while the steady state concentration factors (CFss) were similar. The resulting Cs activity that was purged during short- and long-term depuration phases differed, while the remaining activities after thirty-nine days depuration phase (RA39d) were similar. Co-57 depuration was affected by pCO2 conditions: RA39d were found to be significantly higher in oysters reared in normocapnia (pCO2 = 350 μatm) compared to high pCO2 conditions. Co-57 tissue distribution did not differ among the variable pCO2 conditions, while 109Cd and 134Cs accumulated in soft tissue of oysters were found to be higher under the highest pCO2. Additionally, Cd, Co and Cs were stored differently in various compartments of the oyster cells, i.e. cellular debris, metal-rich granules (MRG) and metallothionein-like proteins (MTLP), respectively. The subcellular sequestration of the elements at the end of the depuration phase did not differ among pH treatments. These results suggest that bioconcentration and tissue/subcellular distribution are element-specific in the oyster, and the effects of higher pCO2 driven acidification and/or coastal acidification variably influence these processes.

Bioaccumulation and effects of dietary exposure to the alternative flame retardant, bis(2-ethylhexyl) tetrabromophthalate (TBPH), in the Atlantic killifish, Fundulus heteroclitus.

Bis(2-ethylhexyl) tetrabromophthalate (TBPH), a high production volume flame retardant chemical used as a replacement for banned flame retardants, has been detected in media and human and wildlife tissues globally. We describe bioaccumulation and biological effects from dietary exposure of TBPH to an estuarine fish, Atlantic killifish, Fundulus heteroclitus. Briefly, adult fish were fed carrier control or chemically amended diets for 28 d, followed by 14 d of control diet feeding. Diets were amended with TBPH (TBPH_LO diet, 139 μg/g dry wt, or TBPH_HI diet, 4360 μg/g dry wt) or a polychlorinated biphenyl congener (PCB153 diet, 13 μg/g dry wt), which was included as a positive control for bioaccumulation. Although bioaccumulation of either chemical correlated with fish size, only a small proportion of the TBPH offered (<0.5% total TBPH) had bioaccumulated into TBPH-treated fish by 28 d. In contrast, 24.5% of the PCB153 offered was accounted for in 28-d PCB-treated fish. Although 28-d bioaccumulated concentrations of TBPH differed by sex and treatment, sexes did not differ in their rates of TBPH bioaccumulation, and the time to achieve 50% of 28 d concentration (T1/2 ) was estimated to be 13 d. Depuration rates of TBPH did not differ by sex or treatment, and the time after exposure to achieve T1/2 was estimated to be 22 d. Independent of treatment, male fish grew faster than female fish, but for both sexes reproductive condition (gonadal somatic index) declined unexpectedly over the experimental period. Across treatments, only the TBPH_LO treatment affected growth, reducing male but increasing female growth rates by small amounts relative to respective controls. In summary, our study used very high concentrations of dietary TBPH to contaminate fish tissues above the highest levels reported to date in wild biota, yet we observed few adverse biological effects. Environ Toxicol Chem 2018;37:2350-2360. © 2018 SETAC. This article is a US government work and, as such, is in the public domain in the United States of America.

Aging Influences on the Biokinetics of Functional TiO2 Nanoparticles with Different Surface Chemistries in Daphnia magna.

Nanoparticles functionalized with various surface capping moieties are now widely used in different fields, thus there is a major need to understand the behavior and fate of these nanoparticles in the environment. The present study investigated the biokinetics of fresh titanium dioxide nanoparticles (TiO2 NPs) or TiO2 NPs aged under artificial sunlight (16 h light: 8 h dark) for 1, 3, and 5 days, respectively. Two commercial functionalized TiO2 NPs (with SiO2 coating or SiO2 and polydimethylsiloxane coating) were employed in this study. Dynamic light scattering (DLS), Fourier transform infrared spectroscopy (FT-IR), and contact angle (CA) measurements demonstrated that the surface properties had changed due to the degradation during aging. The biokinetic parameters including dissolved uptake and depuration rate constant as well as bioconcentration factors were calculated by a biokinetic model. All the biokinetic parameters were significantly dependent on the aging process. Further data analysis showed that the CA of the TiO2 NPs affected the uptake rate constant and the fast compartmental efflux, and both CA and hydrodynamic diameter affected the fast compartmental efflux. These results were due to the changes of corresponding indexes during the aging process. Our work highlighted the necessity of monitoring the physicochemical indexes of functionalized NPs during aging in evaluation of their environmental risks.

Tissue-specific bioaccumulation, depuration and metabolism of 4,4′-dichlorodiphenyl sulfide in the freshwater mussel Anodonta woodiana

Polychlorinated diphenyl sulfides (PCDPSs) are considered as a class of sulfur-containing dioxin-like pollutants with ubiquitous occurrence in natural waters and potential ecotoxicity to aquatic organisms. However, to date, no information is available regarding the bioaccumulation and biotransformation of PCDPSs in aquatic species. In this study, the uptake and depuration kinetics of 4,4′-dichlorodiphenyl sulfide (4,4′-di-CDPS) in the freshwater mussel Anodonta woodiana were investigated through semi-static exposure. The uptake rates (k1), depuration rates (k2), biological half-lives (t1/2) and tissue-specific bioconcentration factors (BCFs) of 4,4′-di-CDPS in the gill, liver and muscle were measured in the range of 0.509–21.734 L d−1 g−1 d.w., 0.083–0.221 d−1, 3.14–8.35 d and 3.662 × 103–124.979 × 103 L kg−1 l.w., respectively. With the increase in exposure dose, the values of k1 and BCFs were significantly reduced, indicating that low-dose exposure to 4,4′-di-CDPS could lead to more severe bioaccumulation. Based on the analysis of mass spectra of the extracted liver samples, the structures of four metabolites of 4,4′-di-CDPS were identified. Moreover, the levels of these metabolites were also quantitatively measured. The proposed metabolic pathways of 4,4′-di-CDPS in mussel liver included sulfur-oxidation, dechlorination and methoxylation. Comparatively, sulfur-oxidation was the predominant metabolic pathway of 4,4′-di-CDPS in the liver of A. woodiana. These results provide valuable data and fill the information gap on the bioaccumulation and metabolism of PCDPSs in freshwater species.

Effect of salinity on the bioaccumulation and depuration of cadmium in the pacific cupped oyster, Crassostrea gigas

As a euryhaline species, the oyster Crassostrea gigas can adapt rapid and dramatic salinity fluctuations, and show physiological mechanisms of adaption to tolerant salinity changes. They are continuously exposed to Cd because they are filter feeders and their mobility is poor. In order to understand the influence of salinity on the molecular responses of C. gigas exposed to Cd, oysters were acclimatized to different salinities (13, 20, 27, and 34) for 14 days and then exposed to 10 μg/L Cd for 28 d, followed by a depuration period of 35 d. Control groups were kept at the same salinities without Cd. Oysters were sampled for chemical analysis by inductively coupled plasma mass spectrometry (ICP-MS) and for mRNA quantification by qPCR. The rank order of the mean concentrations of Cd in oyster tissues was digestive gland > mantle > adductor muscle. Use of a two-compartment model showed that in the three tissues, Cd uptake rates (k1) in digestive gland (13.525–35.430 d−1) also increased as salinity decreased. However, no difference was observed in Cd uptake rates of C.gigas in the three higher salinities in mantle (11.703–17.250 d−1). Cd depuration rates (k2) (0.0139 - 0.0127 d-1 in mantle and 0.0111-0.0134 d−1 in digestive gland) followed a reverse trend. There was not a relationship between k2 and salinity in adductor muscle. In response to Cd contamination, MT was significantly up-regulated by Cd at all salinities, and P-gp was significantly up-regulated in mantle, while down-regulated in digestive gland, which means a disruption of the protein synthesis at high concentration. At depuration phase, MT level was higher in digestive gland and mantle, and its expression was higher at S13 than that at S34. No relationship was found between the P-gp gene expression level and concentrations of cadmium in tissues in either accumulation phase or depuration phase. In accumulation phase, the MT gene expression level was positively correlated with the concentration of cadmium in both the digestive gland and the mantle, while the relationship was weakened in depuration phase, suggesting an effort to create a detoxification mechanism.

Toxicokinetics of cadmium in Palaemon varians postlarvae under waterborne and/or dietary exposure.

The present study assessed cadmium uptake and depuration rates in the euryhaline estuarine shrimp Palaemon varians under different exposure routes. Postlarval shrimp were exposed for 4 d under different exposure routes: contaminated water, contaminated diet, and a 2-way exposure scenario where both contaminated water and diet were used. After exposure, postlarval shrimp were transferred to a clean medium and fed a noncontaminated diet for 96 h. Bioaccumulation via the different exposure routes was modeled with a standard first-order, one-compartment toxicokinetics model and one with an additional parameter reflecting an inert fraction or storage compartment. The simultaneous 2-way exposure (through water and diet) resulted in accumulation being almost twice as high as the sum of the individual exposure routes, thus indicating that accumulation from multiple routes may be more than additive. Cadmium uptake from water was faster than uptake from food maintained for 48 h at that same cadmium concentration. Shrimp were unable to eliminate cadmium from their body, showing no depuration during 96 h after exposure via different routes, thus suggesting that a longer depuration period is needed. Model comparisons did not provide a significantly better fit when the model included the presence of an inert fraction. The present study highlights the importance of assessing accumulation using multiple exposure routes compared with individual routes because the latter may underestimate bioaccumulation. Environ Toxicol Chem 2018;37:1614-1622. © 2018 SETAC.

Deriving in Vivo Bioconcentration Factors of a Mixture of Fragrance Ingredients Using a Single Dietary Exposure and Internal Benchmarking.

Chemicals in mixtures that are hydrophobic with Log KOW > 4 are potentially bioaccumulative. Here, we evaluate an abbreviated and benchmarked in vivo BCF measurement methodology by exposing rainbow trout to a mixture of eight test chemicals found in fragrance substances and three benchmark chemicals (musk xylene (MX), hexachlorobenzene (HCB) and PCB52) via a single contaminated feeding event followed by a 28-day depuration period. Concentrations of HCB and PCB52 in fish did not decline significantly (their apparent depuration rate constants, kT, were close to zero), whereas kT for MX was 0.022 d-1. The test chemicals were eliminated much more rapidly than the benchmark chemicals ( kT > 0.117 d-1). The bioconcentration factors (BCFA) for the test chemicals were in the range of 273 L kg-1 (8-cyclohexadecen-1-one (globanone)) to 1183 L kg-1 (α-pinene); the benchmarked BCFs (BCFG) calculated relative to HCB ranged from 238 L kg-1 (globanone) to 1147 L kg-1 (α-pinene). BCFG were not significantly different from BCFA but had smaller standard errors. BCFs derived here agreed well with values previously measured using the OECD 305 test protocol. We conclude that it will be feasible to derive BCFs of chemicals in mixtures using a single dietary exposure and chemical benchmarking.