The ecotoxicity of platinum nanoparticles (PtNPs) widely used in for example automotive catalytic converters, is largely unknown. This study employs various characterization techniques and toxicity end points to investigate PtNP toxicity toward the green microalgae Pseudokirchneriella subcapitata and Chlamydomonas reinhardtii. Growth rate inhibition occurred in standard ISO tests (EC values of 15-200 mg Pt/L), but also in a double-vial setup, separating cells from PtNPs, thus demonstrating shading as an important artifact for PtNP toxicity. Negligible membrane damage, but substantial oxidative stress was detected at 0.1-80 mg Pt/L in both algal species using flow cytometry. PtNPs caused growth rate inhibition and oxidative stress in P. subcapitata, beyond what was accounted for by dissolved Pt, indicating NP-specific toxicity of PtNPs. Overall, P. subcapitata was found to be more sensitive toward PtNPs and higher body burdens were measured in this species, possibly due to a favored binding of Pt to the polysaccharide-rich cell wall of this algal species. This study highlights the importance of using multimethod approaches in nanoecotoxicological studies to elucidate toxicity mechanisms, influence of NP-interactions with media/organisms, and ultimately to identify artifacts and appropriate end points for NP-ecotoxicity testing.

A sediment-type photomicrobial fuel cell (PFC), based on the synergistic interaction between microalgae (Chlorella vulgaris) and electrochemically active bacteria, was developed to remove carbon and nutrients from wastewater, and produce electricity and algal biomass simultaneously. Under illumination, a stable power density of 68 AE 5 mW m À2 and a biomass of 0.56 AE 0.02 g L À1 were generated at an initial algae concentration of 3.5 g L À1 . Accordingly, the removal efficiency of organic carbon, nitrogen and phosphorus was 99.6%, 87.6% and 69.8%, respectively. Mass balance analysis suggested the main removal mechanism of nitrogen and phosphorus was the algae biomass uptake (75% and 93%, respectively), while the nitrification and denitrification process contributed to a part of nitrogen removal (22%). In addition, the effect of illumination period on the performance of PFC was investigated. Except notable fluctuation of power generation, carbon and nutrients removal was not significantly affected after changing the light/dark photoperiod from 24 h/0 h to 10 h/14 h. This work represents the first successful attempt to develop an effective bacteria-algae coupled system, capable for extracting energy and removing carbon, nitrogen and phosphorus from wastewater in one-step.

Glyphosate (Gly) is one of the most problematic pesticides that repeatedly appears in drinking water. Continuous on-site detection of Gly in water supplies can provide an early warning in incidents of contamination, before the pesticide reaches the drinking water. Here, we report the first direct detection of Gly in tap water with electrochemical sensing. Gold working electrodes were used to detect the pesticide in spiked tap water without any supporting electrolyte, sample pretreatment or electrode modifications. Amperometric measurements were used to quantify Gly to a limit of detection of 2 μM, which is below the regulation limit of permitted contamination of drinking water in the United States. The quantification of Gly was linearly proportional with the measured signal. The selectivity of this method was evaluated by applying the same technique on a Gly Metabolite, AMPA, and on another pesticide, omethoate, with a chemical structure similar to Gly. The testing revealed no interfering electrochemical activity at the potential range used for Gly detection. The simple detection of Gly presented in this work may lead to direct on-site monitoring of Gly contamination at drinking water sources.

Pesticides are heavily used in agriculture to protect crops from diseases, insects, and weeds. However, only a fraction of the used pesticides reaches the target and the rest slips through the soil, causing the contamination of ground-and surface water resources. Given the emerging interest in the on-site detection of analytes that can replace traditional chromatographic techniques, alternative methods for pesticide measuring have recently encountered remarkable attention. This review gives a focused overview of the literature related to the electrochemical detection of selected pesticides. Here, we focus on the electrochemical detection of three important pesticides; glyphosate, lindane and bentazone using a variety of electrochemical detection techniques, electrode materials, electrolyte media, and sample matrix. The review summarizes the different electrochemical studies and provides an overview of the analytical performances reported such as; the limits of detection and linearity range. This article highlights the advancements in pesticide detection of the selected pesticides using electrochemical methods and point towards the challenges and needed efforts to achieve electrochemical detection suitable for on-site applications.

Pyocyanin is a toxin produced by Pseudomonas aeruginosa. Here we describe a novel paper-based electrochemical sensor for pyocyanin detection, manufactured with a simple and inexpensive approach based on electrode printing on paper. The resulting sensors constitute an effective electrochemical method to quantify pyocyanin in bacterial cultures without the conventional time consuming pretreatment of the samples. The electrochemical properties of the paper-based sensors were evaluated by ferri/ferrocyanide as a redox mediator, and showed reliable sensing performance. The paper-based sensors readily allow for the determination of pyocyanin in bacterial cultures with high reproducibility, achieving a limit of detection of 95 nM and a sensitivity of 4.30 μA/μM in standard culture media. Compared to the similar commercial ceramic based sensors, it is a 2.3-fold enhanced performance. The simple in-house fabrication of sensors for pyocyanin quantification allows researchers to understand in vitro adaptation of P. aeruginosa infections via rapid screenings of bacterial cultures that otherwise are expensive and time-consuming.