Publications by authors named "Isabelle A Worms"

The microbial community composition in aquatic ecosystems have received increased attention. However, the knowledge gap relative to the responses of bacterial, archaeal and fungal communities in co-contaminated river sediments remain poorly studied. Here, we investigated the changes of tetrabromobisphenol A (TBBPA) and copper (Cu) concentrations and the responses of microbial communities in co-contaminated sediments during long-term incubation.

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The present review critically examines the state-of-the-art of the research concerning the likely environmental implications of engineered nanoparticles (ENPs) with specific emphasis on their interactions with phytoplankton in the aquatic environment. Phytoplankton plays a key role in the global carbon cycle and contributes to the half of the global primary production, thus representing some of the Earth ' s most critical organisms making the life on our planet possible. With examples from our own research and the literature, we illustrate what happens when aquatic organisms are unintentionally exposed to metal-containing ENPs, which are increasingly released into the environment from nano-enabled materials.

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Humic substances (HS) play key role in toxic metal binding and protecting aquatic microorganisms from metal-induced stress. Any environmental changes that could alter HS concentration and reactivity can be expected to modify metal complexation and thus affect metal speciation and bioavailability to microalgae. The present study explores the influence of increased solar irradiance on the chemical structures and molecular weight of Elliott soil humic acid (EHA) and the associated consequences for Cd(II), Cu(II) and Pb(II) complexation and intracellular metal content in microalga.

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Background: Despite numerous studies suggesting that amphibians are highly sensitive to cumulative anthropogenic stresses, the role pollutants play in the decline of amphibian populations remains unclear. Amongst the most common aquatic contaminants, polycyclic aromatic hydrocarbons (PAHs) have been shown to induce several adverse effects on amphibian species in the larval stages. Conversely, adults exposed to high concentrations of the ubiquitous PAH, benzo[a]pyrene (BaP), tolerate the compound thanks to their highly efficient hepatic detoxification mechanisms.

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The present study examines the effect of carboxyl-CdSe/ZnS quantum dots (QDs) on Cu and Pb availability to microalgae with different cell wall characteristics: Chlorella kesslerii possessing a cellulosic cell wall and two strains of Chlamydomonas reinhardtii, a wall-less and a walled strain containing glycoproteins as the main cell wall component. Results demonstrated that QDs decreased Pb and Cu intracellular contents ({Cu}(int) and {Pb}(int)) in walled strains by a factor of 2.5 and 2, respectively, as expected by the decrease of about 70% and 40% in the dissolved Cu and Pb concentrations.

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A general consensus that an increased logK(ow) led to an increase in xenobiotic uptake and bioaccumulation is accepted. In this study we compared the toxicokinetics of two chemically different xenobiotics, i.e.

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The present study provides results on the influence of humic substance (HS) photoalteration on lead availability to the freshwater microalga Chlorella kesslerii . The evolution of the free lead-ion concentrations measured by the ion exchange technique [Pb](IET) and intracellular lead contents was explored in the presence of Suwannee River humic (SRHA) and fulvic (SRFA) acids, as well as Aldrich humic acid (AHA) exposed at increasing radiance doses under a solar simulator. Modifications of HS characteristics highly relevant to Pb complexation and accumulation of HS to algal surfaces, including Fourier transform infrared spectroscopy, were followed.

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Colloidal organic matter from wastewater treatment plants was characterized and examined with respect to its role in metal distribution by using tangential flow ultrafiltration, liquid chromatography coupled with organic carbon and UV detectors, and an asymmetrical flow field-flow fractionation (AFlFFF) multidetection platform. Results revealed that a humic-like fraction of low aromaticity with an average molar mass ranging from 1600 to 2600Da was the main colloidal component. High molar mass fractions (HMM), with molar mass ranges between 20 and 200kDa, were present in lower proportions.

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The present study addresses the key issue of linking the chemical speciation to the uptake of priority pollutants Cd(II) and Pb(II) in the wastewater treatment plant effluents, with emphasis on the role of the colloidal organic matter (EfOM). Binding of Cd(II) and Pb(II) by EfOM was examined by an ion exchange technique and flow field-flow fractionation coupled to inductively coupled plasma mass spectrometry in parallel to bioassays with green microalga Chlorella kesslerii in ultrafiltrate (<1 kDa) and colloidal isolates (1 kDa to 0.45 mum).

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In natural waters, the determination of free metal concentrations is a key parameter for studying bioavailability. Unfortunately, few analytical tools are available for determining Ni speciation at the low concentrations found in natural waters. In this paper, an ion exchange technique (IET) that employs a Dowex resin is evaluated for its applicability to measure [Ni(2+)] in freshwaters.

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It is generally admitted that the presence of major cations and H+ can attenuate trace metal uptake. Recent models such as the biotic ligand model (BLM) aim to quantify and predict this effect by determining stability constants for each of the major competitors for any given interaction of a trace metal with a biological organism. In this study, short-term Ni internalization fluxes (J(int)) were used to quantitatively assess the binding of H+, Mg2+, Ca2+ (K(H-Rs), K(Mg-Rs), K(Ca-Rs)), and trace metals to transport sites (R(s)) leading to Ni biouptake by Chlamydomonas reinhardtii.

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Short-term (< 60 min) internalization fluxes (J(int)) by the green alga Chlamydomonas reinhardtii were measured in the presence of a variety of ligands forming hydrophilic (citric, diglycolic, or nitrilotriacetic acids), amphiphilic (Suwannee River fulvic and humic acids), and hydrophobic (oxine, diethyldithiocarbamate) Ni complexes. Free nickel concentrations, ranging from 10(-10) to 10(-3) M, were evaluated by thermodynamic modeling and by a resin exchange technique. Ni internalization appeared to occur via a single transport site that was characterized by a conditional stability constant (pH 6.

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