Fouling organisms fix and grow on submerged surfaces and may cause several economic losses. Thus, antifouling biocides have been introduced in antifouling paints in order to avoid this phenomenon. However, their widespread use became a global problem, since these substances can be highly toxic to non-target organisms, mainly in high boat traffic areas. The occurrence and environmental behavior of antifouling biocides are especially unknown in areas of ecological relevance, as Amazonian and pre-Amazonian regions. Thus, the aim of this work was to evaluate, for the first time, levels and the partitioning behavior of the antifouling organic biocides irgarol, diuron and also stable degradation products of dichlofluanid and diuron (DMSA and DCPMU, respectively) in sediments and porewaters from a high boat traffic area located in the Northeast of Brazil. Our results showed high concentrations of irgarol and diuron in sediments, and their contamination patterns suggested that misuse and discard of antifouling residues contribute for a serious risk in this environment. Additionally, DCPMU and DMSA were detected for the first time in porewaters of the Brazilian coast. This work represents one of the few registers of contamination, especially by antifouling substances, in Amazonian areas, despite their environmental relevance.

Compound-specific isotope analysis (CSIA) was firstly applied to explore the biodegradation of hexachlorcyclohexane (HCH) isomers in contaminated soil. Concentrations and compound-specific carbon isotope ratio profiles of HCH in different specific ex-situ pilot-scale contaminated soil mesocosms were determined. The addition of nutrients and Sphingobium spp. significantly enhanced the degradation of HCH in contaminated soils within 90 days. Isomer specific biodegradation of HCHs was observed with α- and γ-HCH being more degradable than β and δ-HCH. Stable carbon isotope fractionation of HCH was observed and the δ¹³C values shifted from −28.8 ± 0.3‰ to −24.8 ± 0.7‰ upon 87.3% removal, −27.9 ± 0.2‰ to −25.9 ± 0.5‰ upon 72.8% removal, −29.4 ± 0.3‰ to −19.9 ± 0.6‰ upon 95.8% removal, and −27.8 ± 0.5‰ to −23.6 ± 0.7‰ after 96.9% removal for α, β, γ, and δ-HCH, respectively. Furthermore, the enrichment factor ε for α, β, γ, and δ-HCH biodegradation in soil was obtained for the first time as −2.0‰, −1.5‰, −3.2‰, and −1.4‰, which could play a critical role in assessing in situ biodegradation of HCH isomers in field site soil. Results from ex-situ pilot-scale experiments clearly demonstrated that CSIA could be a promising tool to qualitatively and quantitatively evaluate in situ biodegradation of HCH in contaminated field site.

Exploring traditional neonicotinoid pesticides substitutes has become one of the global scientific attentions because of their hazardous environmental impacts. Cycloxaprid (CYC) is considered to be a promising candidate alternative. But the environmental behaviors and fate of CYC in different planting system remain poorly understood. The accumulation of 14C-labeled CYC stereoisomers within different parts of Chinese cabbage (Brassica chinensis L.) was investigated, with a particular focus on the foliar absorption, translocation and stereoselectivity of CYC, during a laboratory trial. In general, the stereoisomers 14C-5R,8S-CYC and 14C-5S,8R-CYC, their metabolites, as well as the breakdown and reaction products can be transferred in both acropetal and basipetal directions. Most of the two stereoisomers absorbed by plants remained in the treated leaves, whereas a small amount was distributed to the roots. The amount of 14C in the stalks varied among the experimental time points. At 192 h after treatment (HAT), the detected radioactivity of both 14C-5R,8S-CYC and 14C-5S,8R-CYC in the leaves above the treated leaf (LATL) was higher than that in the leaves below the treated leaf (LBTL). However, the stereoisomers of CYC underwent nonstereoselective absorption and translocation in this trial. This information implies that racemic CYC and its metabolites should be a main research focus. Thus, the obtained results provide implications for a more accurate prediction about the risk assessment of CYC, which will be helpful for guiding its rational use as well as securing the ecological environment safety and human health.

Appropriately characterizing spatiotemporal individual mobility is important in many research areas, including epidemiological studies focusing on air pollution. However, in many retrospective air pollution health studies, exposure to air pollution is typically estimated at the subjects’ residential addresses. Individual mobility is often neglected due to lack of data, and exposure misclassification errors are expected. In this study, we demonstrate the potential of using location history data collected from smartphones by the Google Maps application for characterizing historical individual mobility and exposure. Here, one subject carried a smartphone installed with Google Maps, and a reference GPS data logger which was configured to record location every 10 s, for a period of one week. The retrieved Google Maps Location History (GMLH) data were then compared with the GPS data to evaluate their effectiveness and accuracy of the GMLH data to capture individual mobility. We also conducted an online survey (n = 284) to assess the availability of GMLH data among smartphone users in the US. We found the GMLH data reasonably captured the spatial movement of the subject during the one-week time period at up to 200 m resolution. We were able to accurately estimate the time the subject spent in different microenvironments, as well as the time the subject spent driving during the week. The estimated time-weighted daily exposures to ambient particulate matter using GMLH and the GPS data logger were also similar (error less than 1.2%). Survey results showed that GMLH data may be available for 61% of the survey sample. Considering the popularity of smartphones and the Google Maps application, detailed historical location data are expected to be available for large portion of the population, and results from this study highlight the potential of these location history data to improve exposure estimation for retrospective epidemiological studies.

As the frequency, intensity, and duration of heatwaves increases, emergency health serviceutilization, including ambulance service, has correspondingly increased across the world. The negative effects of air pollution on health complicate these adverse health effects. This research work is the first known study to analyze the joint effects of heatwaves and air quality on the ambulance service in Western Australia (WA). The main objective is to investigate the potential joint effects of heatwaves and air quality on the ambulance service for vulnerable populations in the Perth metropolitan area. A time series design was used. Daily data on ambulance callouts, temperature and air pollutants (CO, SO₂, NO₂, O₃, PM₁₀ and PM₂.₅) were collected for the Perth metropolitan area, WA from 2006 to 2015. Poisson regression modeling was used to assess the association between heatwaves, air quality, and ambulance callouts. Risk assessments on age, gender, socio-economic status (SES), and joint effects between heatwaves and air quality on ambulance callouts were conducted. The ambulance callout rate was higher during heatwave days (14.20/100,000/day) compared to non-heatwave days (13.95/100,000/day) with a rate ratio of 1.017 (95% confidence interval 1.012, 1.023). The ambulance callout rate was higher in males, people over 60 years old, people with low SES, and those living in coastal areas during period of heatwaves. Exposure to CO, SO₂, O₃ and PM₂.₅ increased risk on ambulance callouts and exposure to NO₂ showed joint effect with heatwave and increased risk of ambulance callouts by 3% after adjustment of all other risk factors. Ambulance callouts are an important indicator for evaluating heatwave-related emergency morbidity in WA. As the median concentrations of air pollutants in WA were lower than the Australian National Standards, the interactive effects of heatwaves and air quality on ambulance service need to be further examined, especially when air pollutants exceed the standards.

Perfluoroalkyl acids (PFAAs) are persistent in the environment, highly bio-accumulative in the body, and likely hepatotoxic in humans. There is evidence of sex-specific physiological responses to PFAA exposure. However, epidemiological studies seldom stratify the analyses by sex. Given the high prevalence of liver disease in general population adolescents, this study was designed to determine whether or not there is association between exposure to PFAAs and biomarkers of liver function in adolescent participants of the 2013–2016 National Health and Nutrition Examination Survey, and whether or not such association is sex-specific. Multivariate linear regressions were performed to examine the association between single PFAAs [perfluorooctane sulfonic acid (PFOS); linear form of perfluorooctanoic acid (PFOA); perfluorohexane sulfonic acid (PFHxS); perfluorononanoic acid (PFNA)], and biomarkers of liver function — gamma glutamyltransferase (GGT), aspartate aminotransferase (AST), alanine aminotransferase (ALT), and total bilirubin. Multivariate logistic regressions were performed to estimate adjusted odd ratios (aOR) of elevated ALT, AST and GGT. The study results show that, in females, there was a positive association of the highest PFOA quartile with increased ALT, AST and GGT, and the highest PFNA quartile with increased ALT and AST. Conversely, in male adolescents there was an association of the highest linear PFOA quartile with decreased ALT, and the highest PFNA quartile with ALT and AST. Females had higher odds of clinically-defined elevated ALT with increased PFOA (aOR = 1.79; 95% CI: 1.05, 3.04) or PFNA (aOR = 2.28; 95% CI: 1.08, 2.28), whereas males had decreased odds of clinically-defined elevated ALT with increased n-PFOA (aOR = 0.43; 95% CI: 0.20, 0.93) or PFNA (aOR = 0.5; 95% CI: 0.28, 0.89). In conclusion, there were sex differences in the association between serum PFAA levels and biomarkers of liver function. These results may provide support for analyzing sex-based adverse effects of PFAAs.

The present study aimed to elucidate the mechanisms of organismal sensitivity and/or physiological adaptation in the contaminated water environment. Multigenerational cultures (F0, F1, F2) of Daphnia magna in collected stream water (OCSW), contaminated with high fecal coliform, altered the reproductive scenario (changes in first brood size timing, clutch numbers, clutch size etc.), compromised fitness (increase hemoglobin, alteration in behavior), and affected global DNA methylation (hypermethylation) without affecting survival. Using proteomics approach, we found 288 proteins in F0 and 139 proteins in F2 that were significantly differentially upregulated after OCSW exposure. The individual protein expressions, biological processes and molecular functions were mainly related to metabolic processes, development and reproduction, transport (protein/lipid/oxygen), antioxidant activity, increased globin and S-adenosylmethionine synthase protein level etc., which was further found to be connected to phenotype-dependent endpoints. The proteomics pathway analysis evoked proteasome, chaperone family proteins, neuronal disease pathways (such as, Parkinson's disease) and apoptosis signaling pathways in OCSW-F0, which might be the cause of behavioral and developmental alterations in OCSW-F0. Finally, chronic multigenerational exposure to OCSW exhibited slow physiological adaptation in most of the measured effects, including proteomics analysis, from the F0 to F2 generations. The common upregulated proteins in both generations (F0 & F2), such as, globin, vitellinogen, lipid transport proteins etc., were possibly play the pivotal role in the organism's physiological adaptation. Taken together, our results, obtained with a multilevel approach, provide new insight of the molecular mechanism in fecal coliform-induced phenotypic plasticity in Daphnia magna.

Stressors associated with climate change and contaminants, resulting from the activities of humans, are affecting organisms and ecosystems globally. Previous studies suggest that the unique characteristics of polar biota, such as slower metabolisms and growth, and the generally stable conditions in their natural environment, cause higher susceptibility to contamination and climate change than those in temperate and tropical areas. We investigated the effects of increased temperature and decreased salinity on copper toxicity in four subantarctic marine invertebrates using realistic projected conditions under a future climatic change scenario for this region. We hypothesised that these relatively subtle shifts in environmental stressors would impact the sensitivity of cold-adapted species to copper. The four test species were: a copepod Harpacticus sp.; isopod Limnoria stephenseni; flatworm Obrimoposthia ohlini; and bivalve Gaimardia trapesina. These species occupy a range of ecological niches, spanning intertidal and subtidal nearshore zones. We predicted that species would differ in their tolerance to stressors, depending on where they occurred within this ecological gradient. Organisms were exposed to the multiple stressors in a factorial design in laboratory based toxicity tests. Sensitivity estimates for copper (LC50) were calculated using a novel statistical approach which directly assessed the impacts of the multiple stressors. In three of the four species tested, sensitivity to copper was amplified by small increases in temperature (2-4 °C). The effects of salinity were more variable but a decrease of as little as 2 ppt caused a significant effect in one species. This study provides some of the first evidence that high latitude species may be at increased risk from contaminants under projected future climate conditions. This interaction, between contaminants and the abiotic environment, highlights a potential pathway to biodiversity loss under a changing climate.

The effect of selenium (Se) on the reproductive system has been investigated in both humans and vertebrates, but few studies of female fertility and reproduction in invertebrate have been reported. This study is aimed to investigate the effect of SeMet on growth performance and reproductive system after crayfish were fed with graded levels of dietary SeMet (0, 1.49, 3.29, 10.02, 30.27 or 59.8 μg Se/g dry weight) for 60 days. Crayfish treated with the high levels of SeMet (10.02, 30.27 and 59.76 μg Se/g) exhibited decreasing FW and CL in both male and female. Interestingly, Se accumulation was higher in ovary than in other tissues, suggesting that ovary may serve as a target organ for Se accumulation. We found that dietary Se concentration of 10.02 μg Se/g significantly improved the spawning rate, promoted the synchronized spawning, and up-regulated the expressions of mRNA of cdc2 and vitellogenin, with significantly increased E2 and VTG concentrations in hemolymph of female crayfish. However, a marked decrease of the E2 contents and spawning rate was observed in the groups treated with 30.27 and 59.76 μg Se/g diets. In conclusion, the results of this study indicated that the Se had maximum accumulation in ovary, affecting the reproductive capacity by intervening the expression of cdc2 and vitellogenin in the reproductive system. The LOAEL to induce FW was observed in crayfish fed with 10.02 μg Se/g diet, and its value can cause toxicity within the range of natural concentration, so the addition of Se in the feed should be within 10.02 μg Se/g.

Microcystin-LR (MCLR) is the most commonly encountered toxic microcystin variant. MCLR is usually present along with common surface water constituents such as inorganic ions and natural organic matter (NOM) which compete with MCLR for active sites during ion exchange (IX) process. Consequently, development of a multicomponent competitive model is essential for practical IX applications. This is critically important given that the NOM characteristics (charge density and molecular weight distribution) and inorganic ions concentrations are spatially variable and can change seasonally. In the present study, a systematic study was carried out into the multicomponent interactions of IX resin with inorganic ions and NOM during the MCLR removal process. This involved evaluation of MCLR removal in a single component system (i.e., MCLR only), a dual component system (MCLR and one other contaminant such as NOM), and a multiple component system (MCLR with NOM and different inorganic ions present in natural waters). A comprehensive understanding of the dynamic adsorption behavior showed that the experimental data for single component systems agree well with a Freundlich isotherm. For multicomponent interactions, the Equivalent Background Concentration (EBC) model which is derived from the Ideal Adsorption Solution Theory (IAST) provided the best correlation with the experimental data in natural waters. The concentrations of competing NOM and inorganic ions estimated by the EBC model were <10% of their initial concentrations. Sulphates are the most competitive inorganic ions followed by nitrates and bicarbonates and the multicomponent interactions could be well predicted by using the IAST-EBC model. However, the EBC model failed in the presence of higher molecular weight Suwannee River Humic Acid (SRHA) molecules due to neglecting of the pore blocking phenomenon. In the presence of higher molecular weight SRHA molecules, the Redlich-Peterson Isotherm (RP) model exhibited a better performance than the Sheindorf–Rebuhn–Sheintuch (SRS) and the EBC models.