Explore the vast range of titles available.

Pyriproxyfen is an insect growth regulator acting as larvicide against a large spectrum of public health insect pests, especially dipterans. It is also widely used in agriculture and horticulture for the control of many insect species. Disrupting the endocrine system by mimicking the activity of the juvenile hormone, pyriproxyfen interferes with metamorphosis in insects and prevents them from reaching maturity and reproducing. Because the aquatic ecosystems can be directly or indirectly contaminated by pyriproxyfen, the goal of this study was to establish the aquatic ecotoxicological profile of pyriproxyfen and to identify the gaps that need to be filled. Pyriproxyfen is photodegraded quickly in water. In the absence of organic matter, its persistence in aerobic water media is also limited especially with high temperature and sunlight. Analysis of the laboratory and in situ results for more than 60 aquatic algae, plants, invertebrates, and vertebrates shows that the toxicity of pyriproxyfen is highly variable including within a same taxonomical group. Abiotic and biotic factors can highly influence the toxicity of the molecule. Pyriproxyfen disrupts the development of numerous species and adversely impacts various physiological events. It can also disturb the behavior of the organisms such as their predatory and swimming performances. Although some experimental studies focus on the environmental fate of pyriproxyfen metabolites, those dealing with their aquatic ecotoxicity assessment are scarce. In the same way, the limited number of studies dealing with the search of pyriproxyfen residues in lake, river, and other natural aquatic media does not include the identification of the metabolites.

In situ burning is a method by which oil is burned at a spill site under controlled conditions, and this method is subject to increased interest due to its applicability in the Arctic. This paper reviews the literature regarding the characterization and environmental effects of burn residues in Arctic waters. The results of a systematic literature search indicate that only a very limited number of studies have arctic pertinence. From the review, it is also indicated that the properties and composition of the residues depend on the efficiency of the burning and the oil type. Furthermore, the studies within the frame of the literature search reach consensus that in situ burning may increase the concentrations of large poly-aromatic hydrocarbons (PAHs; high ring number) while reducing small PAHs (low ring number). There are very few toxicity studies of burn residues on aquatic and arctic organisms, and to enhance the knowledge base, more organisms as well as oil types must be studied. Furthermore, there is a lack of studies investigating the potential effect of sinking burn residues on benthic organism and the smothering effects of the more viscous burn residues on birds and other organisms related to the sea surface. More knowledge regarding environmental fate and effect of residues is crucial to complete a robust net environmental benefit analysis prior to an oil spill response operation in arctic waters.

BackgroundLupin is a promising legume crop, belongs to the Fabaceae (or Leguminosae) family. Lupin production for traditional and functional foods or animal feed is limited, due to the content of toxic quinolizidine (QA)s and indole alkaloids (IA)s. These compounds may not only pose a risk to humans and animals through food consumption, but may also affect soil and aquatic ecosystems. Field experiments were conducted to study the alkaloids content in both narrow-leaved or blue (L. angustifolius) and yellow (L. luteus) lupin plant tissue during a full growing season and understand the environmental fate of alkaloids in soil and water. Suction cups were used to collect soil pore water (soil solution) at four depths: 10, 25, 50 and 70 cm. A full protocol for sample preparation and UPLC–MS/MS quantification of alkaloids in plant, soil and water was developed.ResultsDuring the field experiments the alkaloids in the plant tissues increased, at the harvest stage the content was highest with 21.4 and 24.6 mg/kg dry weight (dw) for blue and yellow lupin, respectively. In soil, alkaloids quantified during the growing season (max concentration was 1.3 × 102 µg/kg dw) and even detected after harvest (0.2 µg/kg dw). In soil pore water samples, alkaloids were not detected during summer, but the concentrations increased to 9.8 × 102 and 1.5 × 103 ng/L for blue and yellow, respectively, in September when autumn precipitation began.ConclusionsThe results show the amount of alkaloids transferred from plant tissue into soil and soil pore water estimated to be on average 0.016% and 0.005% in soil and soil pore water, respectively. Alkaloids leached from topsoil to subsoil layers; the concentrations decline with soil depth. This study demonstrates that alkaloids are mobile compounds in the soil environments, thus lupin production may affect soil or aquatic ecosystems, and reduce water quality.

This section covers research published during the calendar year 2018 on mixing and transport processes. The review covers mixing of anaerobic digesters, mixing of heat transfer, and environmental fate and transport.

The sources and environmental fate of polycyclic aromatic hydrocarbons (PAHs) are closely related with anthropological activities and natural environmental conditions. The continental shelf of China Sea has the most intense land-ocean interactions. The PAHs’ distribution in this region is of great significance for revealing the impact of human activities on the marine environment and the environmental fate of terrigenous substances input to the ocean. However, up to now, almost all the studies were confined to relatively small regions, such as estuaries. There was a lack of systematic understanding of PAHs in the whole continental shelf sea. In this study, the relevant research findings of PAHs in the continental shelf of China Sea in recent years were systematically summarized. The spatial and temporal variations of PAHs in sediments of China Sea were comprehensively displayed. The relationships between PAHs’ distributions in different seas with regional economic development history were analyzed. These findings will play a guiding significance for improving marine environment research in large-scale areas.

The long-range transport (LRT) of organic chemicals in the environment is reviewed, with particular focus on the role of environmental fate and transport models and the relationship between model results and field data. Results from generic multimedia box models, spatially resolved multimedia box models, and atmospheric transport models are highlighted, including conceptual investigations of cold-trap effect and global fractionation as well as results for particular chemicals, such as hexachlorocyclohexanes, DDT, polychlorinated biphenyls, perfluoroocctanoic acid, and polybrominated diphenyl ethers. Comparison of model results to field data shows that in many cases environmental fate models provide a good description of the distribution dynamics observed in the field, with deviations between measured and modeled concentrations around a factor of five. Sorption to atmospheric aerosols as a key process influencing the LRT of semivolatile organic chemicals (SOCs) is discussed, and the need for more measurements of the aerosol-air partitioning of SOCs and of the reactivity of particle-bound chemicals is pointed out. Key findings from field campaigns measuring legacy persistent organic pollutants (POPs) as well as new POPs are summarized. Finally, the relationship between science and politics in the field of POPs is addressed. Research into the LRT of organic chemicals has always occurred in interaction with political activities aiming to reduce the emissions of POPs. Since the late 1990s, the Stockholm Convention and the Aarhus Protocol on POPs have formed an important political context for research concerning POPs; the implementation of these international treaties creates a demand for ongoing research into the LRT of organic chemicals.

Biosynthetic toxic compounds from plants and cyanobacteria constitute a chemically diverse family of at least 20,000 compounds. Recent work with natural toxin databases and toxin characterization shows that the majority of natural toxins are polar and mobile, with toxicity ranging from low to very high, while persistence is highly variable. Natural toxins may be produced in high quantities—some exceeding 10 g/m2/year—resulting in high environmental loads. Recent phytotoxin monitoring indicates that one or more natural toxin is always present in a surface water sample, but that concentrations are highly variable often with pulses during rain events. Phytotoxins belong to many classes, but often with flavonoids and alkaloids dominating. Likewise, advanced monitoring discovers a wide spectrum of cyanobacterial metabolites that are released directly into surface waters during water blooms. Except of the few known cyanobacterial toxins, we have very limited info regarding their environmental fate and toxicity.The 16 papers in this article collection present examples of natural toxin occurrence, properties, fate and toxicity. The overarching conclusion is that natural toxins should be monitored and characterized regarding their risk potential, and that natural toxins of greatest expected risk should be evaluated as thoroughly as industrial xenobiotics. Cyanotoxins are well known water contaminants that should be removed for producing drinking water, while for phytotoxins the current knowledge base is very limited. We advocate to intensify research on natural toxins, and to address the evident knowledge gaps on natural toxin analysis/monitoring, physical–chemical properties and degradation/pathways, transport modelling, and toxicity. The complex and dynamic interplays between biotic and site conditions such as vegetation, toxic plant densities, climate, soil types, nutrients and radiation, play decisive roles for both biotoxin formation and fate. Environmental and toxicological research in biosynthesized compounds extends beyond natural toxins, with important perspectives for risk assessment of biopesticides, growth regulators and biomedicine (or biologicals collectively) produced by plants and microorganisms.

The synthetic hormone sodium levothyroxine (LTX) is one of the most prescribed drugs in the world and the most effective in hypothyroidism treatment. The presence of LTX in the environment has become a matter of major concern due to the widespread use of this hormone and by the fact that it is only partially removed in conventional water and sewage treatment plants. However, information regarding the photochemical fate of this hormone in environmental or engineered systems is scarce in the literature. In this work, the sunlight-driven direct and indirect LTX degradation was investigated by determining the photolysis quantum yield, Φ LTX  = 3.80 (± 0.02) × 10 −5 , as well as the second-order kinetic constants of the reactions with hydroxyl radicals, k LTX,•OH  = 1.50 (± 0.01) × 10 10  L mol −1  s −1 and singlet oxygen, k LTX,1O2  = 1.47 (± 0.66) × 10 8  L mol −1  s −1 . Mathematical simulations indicate that LTX photodegradation is favored in shallow, nitrite-rich, and dissolved organic matter (DOM)-poor environments, with LTX half-life times varying from less than 10 days to about 80 days. LTX removals of 85 and 95% were achieved by UVC photolysis and UVC/H 2 O 2 after 120 min, respectively. Three transformation products, triiodothyronine, diiodothyronine, and diiodotyrosine, were identified during LTX degradation by the UVC-based processes studied. The results herein regarding photo-induced kinetics coupled with environmental fate simulations may help evaluate LTX persistence and also the design of water and wastewater treatment processes.

Equilibrium Quality Criterion (EQC) Level I calculations have been performed with Standard Equilibrium Quality Criterion (EQC) environment to study the environmental partitioning of a fungicide Fluopyram. Equilibrium Quality Criterion (EQC) Level I calculation assumes no degradation of the chemical, steady-state, and equilibrium conditions between the environmental compartments. The results reveal that the concentration of Fluopyram is expected to be maximum in the sediment compartment, followed by soil and water compartments. The effect of soil and sediment types on partitioning has been studied by systematically varying the densities of these two compartments. In the sediment compartment, the Fluopyram concentration is predicted to be highest if the sediment type is ‘sandy’ and the soil type is ‘clay’.

Microplastics are the major environmental health hazards spotted in almost all the marine habitats and biota of world. The earlier research on microplastics have mainly focused on studying abundance and distribution as well as impacts on organisms, while the existing review articles have reviewed on any one of the above aspects or the environmental fate of microplastics. The current review focuses on all the above facets thereby bringing out the incompleteness in information globally in the respective facets. Our findings suggest that among 192 countries of the world, only 22.9% (44) of the countries have carried out research regarding microplastics, while impacts on organisms have mostly targeted fish (38%), whereas studies on other highly affected organisms such as turtles (1%) are not well documented. Therefore, we suggest expanding research in all the above aspects of microplastics considering that there are several pristine marine environments and organisms that are yet unexplored. Quantifying research in these regards would enable to propose a microplastic threshold level and formulate control measures to reduce the use of plastics and its subsequent threat to the marine environment.