Depuration of ingested 14C-labelled polystyrene nanospheres in the Atlantic scallop (Placopecten magellanicus).

The presence of nano-plastics in marine bivalves is well established and may represent a risk to human consumption. The main objective of our work was to study the detailed tissue distribution of 14C-radiolabelled polystyrene nanospheres (PSNP; 325 nm) following their ingestion by commercial-size Atlantic scallop (Placopecten magellanicus) using whole-body autoradiography to assess their translocation, bioaccumulation and depuration mechanisms over a short-term exposure (6h) and a long-term exposure (2 weeks). Results showed that the nanospheres (PSNP) did not accumulate in scallop tissues despite the fact they were ingested and transported all along the digestive system. Elimination of the PSNP was virtually completed within 48 h and no radiolabeling appeared in the edible adductor muscle. This is indicative of the presence of an active depuration mechanism of particles without nutritional value as plastic PSNP. Our preliminary work indicates a rapid translocation of PSNP in scallops minimizing a possible transfer to human consumers.

Distribution and Fate of Ultraviolet Absorbents and Industrial Antioxidants in the St. Lawrence River, Quebec, Canada.

Ultraviolet absorbents (UVAs) and industrial antioxidants (IAs) are contaminants of emerging concern. In this study, we investigated the distribution and partitioning of these contaminants in surface water, suspended particulate matter (SPM), sediment, and various tissues of lake sturgeon (Acipenser fulvescens) and northern pike (Esox lucius) from the St. Lawrence River (SLR), Quebec, Canada. Results indicated that 2,6-di-tert-butyl-1,4-benzoquinone (BHTQ) was the dominant contaminant in the dissolved phase of the surface water, with median concentrations of 43, 15, and 123 ng/L for three sampling sites, respectively. Surface water collected downstream of a major city showed higher levels of various UVAs, BHTQ, and diphenylamine compared to the upstream, suggesting the influence of the urban activities on the contamination of these emerging contaminants in the SLR. SPM showed greater sorption capacities of most target contaminants compared to those of the sediment. Different contamination profiles were found in lake sturgeon and northern pike, implying that the accumulation of UVAs and IAs in fish depends on their feeding behavior. The field-based tissue-specific bioaccumulation factors (BAFs) for frequently detected contaminants (log BAF 1.5-4.2) were generally comparable to or lower than the Estimation Program Interface modeling results (1.4-5.0), indicating that some of these contaminants may be less bioaccumulative than previously expected.

Origin of nitrate and sulfate sources in volcano-sedimentary aquifers of the East Africa Rift System: An example of the Ali-Sabieh groundwater (Republic of Djibouti).

Within the East African Rift System (EARS), the complex Ali-Sabieh aquifers system, located in the south of the Republic of Djibouti, was overexploited and subjected to anthropogenic and/or geogenic pollution with high concentrations of dissolved nitrate (up to 181 mg/l) and sulfates (up to 1540 mg/l). This study is the first undertaken on the hydrochemistry of this aquifer system, combining geochemical tools and multi-isotope - δ2H(H2O), δ18O(H2O), δ18O(SO4), δ34S(SO4), δ15N(NO3), δ18O(NO3), δ13C(DIC), and 14C- was used to decipher the origin and fate of different nitrate and sulfate sources to groundwater. The groundwater samples of the region show a chemical evolution from fresh Ca(Na)-bicarbonate to brackish Na-Cl , mainly due to water-rock interaction. The combined chloride and water isotope data show that evaporation and transpiration are present, with the latter occurring primarily in the shallow alluvial aquifer waters. Inspection of δ15N(NO3) vs. δ18O(NO3) and NO3/Cl vs. Cl diagrams show that dissolved nitrates are primarily of anthropogenic origin. In particular, higher nitrate concentrations may be related to animal manure used as organic fertilizers during agricultural activities. Sulfates are from a natural origin related to the interaction of water with gypsum of hydrothermal or sedimentary origin. SO4/Cl ratio and isotopic composition show that dissolved sulfates in saline and ancient groundwater of the Cretaceous sandstone aquifer (between 7.4 ± 2.2 and 5.8 ± 1.4 k-years before the present) are generated by interaction with gypsum from oxidation of pre-existing (Jurassic?) sulfides. This work highlight that isotopic ratios of the two molecules -δ18O(SO4), δ34S(SO4), δ15N(NO3), δ18O(NO3)- are not sufficient for tracing the origin of nitrate and sulfates in groundwater, but that a complete hydrogeochemical study is needed. In the absence of this, the relatively high concentration of chloride and sulfates could be wrongly linked to the anthropogenic source of nitrate (manure or sewage).

Radiolabeling of amide functionalized multi-walled carbon nanotubes for bioaccumulation study in fish bone using whole-body autoradiography.

Commercial and medicinal applications of functionalized carbon nanotubes (f-CNTs) such as amidated f-CNTs are expanding rapidly with a potential risk exposure to living organisms. The effects of amidated f-CNTs on aquatic species have received a limited attention. In this work, an easy wet method to prepare [14C]-label amide multi-walled carbon nanotubes (MWNTs) is reported. Labeled carbon nanotubes were prepared by successive reactions of carboxylation, chloroacylation, and final amidation using [14C]-labeled ethanolamine. The f-CNTs were characterized using elemental analysis, electron dispersive X-ray, transmission electron microscopy, thermogravimetric analysis, and Raman and FTIR spectroscopy. An uptake experiment was carried out with juvenile Arctic char (Salvelinus alpinus) using water dispersed amidated [14C]-f-CNTs to assess their biodistribution in fish tissues using whole body autoradiography. The radioactivity pattern observed in fish head suggests that f-CNTs were accumulated in head bone canals, possibly involving an interaction with mineral or organic phases of bones such as calcium and collagen. This f-CNTs distribution illustrates how important is to consider the surface charges of functionalized carbon nanotubes in ecotoxicological studies.

Sorption and competition of two persistent organic pesticides onto marine sediments: Relevance to their distribution in aquatic system.

Sorption is a key process in the distribution of substances between environmental compartments in marine ecosystems. Two persistent organic pesticides, also known as toxaphene congeners, namely B8-1413 (P26) and B9-1679 (P50), are of special interest because they are not detected in sediments while relatively concentrated in marine mammals. Sorption-desorption, entrapment and competition behaviors of these pesticides onto marine sediments were studied to explain their environmental distribution. Data obtained under marine experimental conditions were fitted to sorption models to evaluate sorption coefficients and to assess the degree of B8-1413/B9-1679 entrapment of the two toxaphene congeners in sediments. Carbon normalized sorption coefficients (Koc) of both congeners were similar under in cold (2°C) marine (30 psu) conditions with high values ranging from 1.53×10(5) to 3.28×10(5) mL g(-1)indicative of a strong affinity to marine sediments However, the sorption-desorption investigations indicate that B8-1413/B9-1679 were on average 2.5 times less entrapped in sediments compared to B7-1450, a toxaphene congener known to accumulate predominantly in sediments. These results suggest that the low entrapment of B8-1413 and B9-1679 favor their availability and transfer to biological matrices.

Sorption behaviors of a persistent toxaphene congener on marine sediments under different physicochemical conditions.

Sorptive processes are important parameters affecting the mobility, availability and fate of persistent organic pollutants (POPs), such as toxaphene, in aquatic systems. The sorption and desorption behaviors of the B7-1450, a stable toxaphene congener in environment, on marine sediment was studied under different temperature and salinity conditions to better understand the B-1450 distribution in estuarine systems. The data were fitted to different sorption models to characterize sorption behaviors by evaluating sorption coefficients and sequestrated fraction of B7-1450 on sediments. High carbon-normalized sorption coefficients (Koc) of the B7-1450 were observed with values ranging from 3.2×104 to 6.0×104 mL g(-1) under experimental conditions. The data showed an increase of B7-1450 sorption coefficients with the salinity and a decrease with temperature. These investigations indicate that B7-1450 is three times more sequestred on sediments in cold (2°C, 30 psu) than in warm marine conditions (20°C, 30 psu). These results suggest that the mobility and bioavailable of B7-1450 or other POPs from the sediments could be less important in cold marine comparatively in warm marine and warm freshwater media. As a result of climate changes, the warming of mid and high latitudes coastal waters could enhance the mobility of POPs.

Wastewater reclamation using discarded reverse osmosis membranes for reuse in irrigation in Djibouti, an arid country.

The purpose of this paper is to establish the feasibility of recovering discarded reverse osmosis (RO) membranes in order to reduce the salinity of domestic treated wastewater. This study shows that the reuse of RO membranes is of particular interest for arid countries having naturally high mineralized water such as Djibouti. The pilot desalination unit reduces the electrical conductivity, the turbidity and the total dissolved salt respectively at 75-85, 96.7 and 95.4%. The water produced with this desalination unit contains an average of 254 cfu/100 mL total coliforms and 87 cfu/100 mL fecal coliforms. This effluent meets the World Health Organization standards for treated wastewater reuse for agricultural purposes. The annual cost of the desalination unit was evaluated as US $/m(3) 0.82, indicating the relatively high cost of this process. Nevertheless, such processes are required to produce an effluent, with a high reuse potential.

Investigations on the sorption of a toxaphene model congener, the B7-1450, on marine sediments.

Sorption is a natural process that takes place in sediments or soils and changes the mobility and availability of hydrophobic organic compounds, such as toxaphene pesticide in the environment. The sorption of the 2-exo,3-endo,5-exo,8,9,10,10-heptachlorobornane (B7-1450), used as a model compound of the toxaphene heptachlorobornane congeners found in sediments, was investigated for the first time through a series of batch sorption experiments. The losses of B7-1450 due to adsorption onto glass walls and to evaporation occurring during analytical treatment steps were corrected. The study showed that these specific losses ranged from 2% to 3.5% for the glass walls adsorption and can be as high as 15% for the evaporation treatment. The sorption coefficients, K(d) and K(oc), of B7-1450 could be overestimated by >30%, particularly for low-concentration samples, if the losses were not corrected. Loss correction equations were established, validated and applied to determine sorption coefficients for the B7-1450 congener. The K(oc) values for B7-1450 determined over a gradient of concentrations ranged from 3.5x10(4) to 6.5x10(4)mlg(-1), revealing a strong affinity of B7-1450 for marine sediments.