A chemical contaminant of growing concern to freshwater aquatic organisms, including many amphibians, is chloride ion. The salinization of freshwater ecosystems is likely caused, in part, by the application of massive amounts of road de-icing salts to roadways during winter months. The issue of freshwater salinization has become the subject of many toxicity studies and is often investigated in conjunction with other chemical stressors. However, few published studies attempt to investigate the interactions of elevated chloride concentration and increased temperature. Further, no studies have investigated the gap between the recommended feeding conditions typically used in standard toxicity tests and those that may exist in natural amphibian habitats. This study addressed the critical issues of elevated chloride, increased temperature, and variation in food quality. We conducted a 96-h acute toxicity test to investigate acute chloride toxicity as impacted by different diets, as well as a chronic toxicity test to investigate the impacts of chloride, temperature, and resource quality on the survival and development of larval Lithobates sylvaticus (wood frogs). Chloride LC₅₀s ± 1 SE were 3769.22 ± 589.05, 2133.00 ± 185.95, and 2644.69 ± 209.73 mg Cl⁻/L were for non-fed, low-protein diet, and high-protein diet, respectively. For the chronic toxicity study, elevated chloride decreased tadpole survival. Increased temperature, and lower resource quality, were found negatively impacted survival of tadpoles and altered time-to-metamorphosis. This study shows that environmentally relevant concentrations of chloride, temperatures, and the protein content of the diet all exert critical effects on larval wood frogs.

In this study, a weather-based multicomponent model was developed based on the unique biostructures and metabolic processes of mushrooms to evaluate their uptake of pesticides from soils, and the effects of temperature and relative humidity on the bioaccumulation of pesticides in mushrooms was comprehensively quantified. Additionally, a new pseudo-partition coefficient between mushrooms and soils was introduced to assess the impacts of different physiochemical properties on the pesticide uptake process. The results indicate that, in general, the pseudo-partition coefficient increases as the relative humidity increases for both the air and soil according to Fick’s law of gas diffusion and the spatial competition of molecules, respectively. Meanwhile, the effect of temperature on the pesticide bioaccumulation process is more complex. For most pesticides (e.g., atrazine), the pseudo-partition coefficient that was computed from the transpiration component had a maximum value at a specific temperature due to the temperature dependency of the transpiration and biodegradation processes. For some pesticides (e.g., ethoprophos), the pseudo-partition coefficient of the air-deposition component had a maximum value at a certain temperature that was caused by the ratio of the soil–air internal transfer energy and degradation activation energy of the pesticide. It was also concluded that for relatively low-volatility pesticides, transpiration dominated the bioaccumulation process; this was mainly determined from the pesticide water solubility. For nonbiodegradable pesticides (e.g., lindane), the computed coefficient values were relatively low due to their insolubility in water, which inhibits bioaccumulation in mushrooms and is one of the main reasons for their long-term persistence in soils.

The m-aminophenol (m-AP) is a widely used industrial chemical, which enters water, soils, and sediments with waste emissions. A common soil metal oxide, birnessite (δ-MnO2), was found to mediate the transformation of m-AP with fast rates under acidic conditions. Because of the highly complexity of the m-AP transformation, mechanism-based models were taken to fit the transformation kinetic process of m-AP. The results indicated that the transformation of m-AP with δ-MnO2 could be described by precursor complex formation rate-limiting model. The oxidative transformation of m-AP on the surface of δ-MnO2 was highly dependent on reactant concentrations, pH, temperature, and other co-solutes. The UV-VIS absorbance and mass spectra analysis indicated that the pathway leading to m-AP transformation may be the polymerization through the coupling reaction. The m-AP radicals were likely to be coupled by the covalent bonding between unsubstituted C2, C4 or C6 atoms in the m-AP aromatic rings to form oligomers as revealed by the results of activation energy and mass spectra. Furthermore, the toxicity assessment of the transformation productions indicated that the toxicity of m-AP to the E. coli K-12 could be reduced by MnO2 mediated transformation. The results are helpful for understanding the environmental behavior and potential risk of m-AP in natural environment.

Nitrogen dioxide (NO₂) is a well-established traffic emissions tracer and has been associated with multiple adverse health outcomes. Short- and long-term exposure to NO₂ has been studied and is well-documented in existing literature, but information on intermediate-term NO₂ effects and mortality is lacking, despite biological plausibility. We obtained daily NO₂ and mortality data from 42 counties in China from 2013 to 2015. Distributed-lag non-linear models were employed to investigate the relationship between non-accidental mortality and NO₂ up to 30 days before the event, including PM₂.₅, temperature, relative humidity, and holidays as covariates in a random effects meta-analysis pooling county-specific estimates. We repeated the analysis for cardiovascular- and respiratory-related mortality, and explored sex-stratified associations. Per 10 μg/m³ increase in NO₂, we estimated a 0.13% (95%CI: 0.03, 0.23%), 0.57% (95%CI: −0.04, 1.18%), and −0.14% (95%CI: −1.63, 1.37%) change in non-accidental mortality for same-day and previous-day NO₂ (lag0-1 cumulated), in the preceding 7 days (lag0-7 cumulated), and in the preceding 30 days (lag0-30 cumulated), respectively. The strongest estimate was observed for respiratory-related mortality in the lag0-30 cumulated effect for women (3.12%; 95%CI: −1.66, 8.13%). We observed a trend of higher effect estimates of intermediate-term NO₂ exposure on respiratory mortality compared to that of the short-term, although the differences were not statistically significant. Our results at longer lags for all-cause and cardiovascular mortality were sensitive to modeling choices. Future work should further investigate intermediate-term air pollution exposure given their potential biological relevance, but in larger scale settings.

This study forms the first basic assessment of microphytobenthos (MPB) dynamics in micro-estuaries and micro-outlets in southern Africa. It examines MPB community responses to environmental variables and further investigates MPB composition qualitatively across different micro-estuaries and micro-outlets over four seasons in a warm temperate region of the subcontinent. Combinations of multivariate analyses were used to explore similarities and differences in MPB communities between systems. Human-induced catchment changes between microsystems ranged from no alteration (rating 0; mostly micro-outlets) to extreme modification (rating 5; mostly micro-estuaries). Two hundred and sixty-seven MPB taxa were identified within all the microsystems, with 247 and 230 MPB taxa being observed in the micro-estuaries and micro-outlets, respectively. The MPB communities differed slightly in terms of microsystem types and seasons, but no significant differences were observed. Multivariate analyses (i.e. Boosted Regression Trees, Canonical Correspondence Analysis) showed that water column variables were significant and important in structuring MPB communities, with soluble reactive phosphorus, sediment pH, turbidity, ammonium and temperature being documented as key drivers. The MPB community composition clearly reflected the influence of catchment anthropogenic activities on species composition and structure. Moderately modified catchments resulted in MPB community structure variation among water bodies in relationship to land use and salinity gradients. The study found that; (i) by virtue of their size, microsystems and their catchments are likely to be particularly vulnerable to anthropogenic pressures when compared to systems of larger size; (ii) a typical impacted state may reflect reduced environmental heterogeneity which, compared to larger systems, may be achieved over much shorter time periods (following a particular event) or under much less intensive impacts; and (iii) the response in terms of MPB structure may predictably reflect a concomitant change from a complex community dynamic (structure and spatio-temporal attributes) to one that approaches a homogeneous structure (poor spatial zonation, strong taxonomic dominance, low species diversity).

Ozone (O₃) is a potent oxidant associated with adverse health effects. Low-cost O₃ sensors, such as metal oxide (MO) sensors, can complement regulatory O₃ measurements and enhance the spatiotemporal resolution of measurements. However, the quality of MO sensor data remains a challenge. The University of Utah has a network of low-cost air quality sensors (called AirU) that primarily measures PM₂.₅ concentrations around the Salt Lake City valley (Utah, U.S.). The AirU package also contains a low-cost MO sensor ($8) that measures oxidizing/reducing species. These MO sensors exhibited excellent laboratory response to O₃ although they exhibited some intra-sensor variability. Field performance was evaluated by placing eight AirUs at two Division of Air Quality (DAQ) monitoring stations with O₃ federal equivalence methods for one year to develop long-term multiple linear regression (MLR) and artificial neural network (ANN) calibration models to predict O₃ concentrations. Six sensors served as train/test sets. The remaining two sensors served as a holdout set to evaluate the applicability of the new calibration models in predicting O₃ concentrations for other sensors of the same type. A rigorous variable selection method was also performed by least absolute shrinkage and selection operator (LASSO), MLR and ANN models. The variable selection indicated that the AirU’s MO oxidizing species and temperature measurements and DAQ’s solar radiation measurements were the most important variables. The MLR calibration model exhibited moderate performance (R² = 0.491), and the ANN exhibited good performance (R² = 0.767) for the holdout set. We also evaluated the performance of the MLR and ANN models in predicting O₃ for five months after the calibration period and the results showed moderate correlations (R²s of 0.427 and 0.567, respectively). These low-cost MO sensors combined with a long-term ANN calibration model can complement reference measurements to understand geospatial and temporal differences in O₃ levels.

Within the outline of air quality studies at metropolitan city, the mixing ratios of seven selected volatile organic compounds (VOCs) were measured during December 2015 (winter) at an urban site of Pune. The measurement of VOCs was conducted using a proton transfer reaction-quadrupole mass spectrometer (PTR-QMS). The study represents daily variability of ambient VOCs and their various associated emission sources. Diurnal profiles have differed from one VOC to another as the result of their different origins and the influence of different meteorological parameters (i.e. solar radiation, temperature) and planetary boundary layer height (PBL-H). The hourly mixing ratios of Oxygenated-VOCs (OVOCs) and aromatics were in the ranges of 0.6–29 ppbv and 0.13–14 ppbv, respectively with OVOCs accounted for up to 75% of total measured VOCs. The role of long-range transport from the clear Thar Desert and polluted Indo-Gangetic Plain (IGP) was observed during the episodes of 1–15 and 17–31 December 2015, respectively. VOCs showed the strong diurnal variations with peaks during morning and evening hours and lowest in the afternoon. In the evening period, high levels of aromatics coincided with the lowest OVOCs suggests the role of fresh vehicular emissions. Emission ratios of various VOCs as a function of temperature showed the role of different sources including the biogenic and photochemical production as well as the anthropogenic sources, respectively. The higher emission ratio of Δmethanol/Δacetonitrile at the study site suggests the long range transport of biomass burning plumes from the Indo-Gangetic Plain (IGP) during the 17–31, Dec. 2015. In addition to the pattern of emission, the diurnal and day-to-day variations of VOCs were influenced by the local meteorological conditions and depth of planetary boundary layer (PBL-H).

Nano-magnetite supported by biochar (nFe₃O₄/BC) pyrolyzed at temperatures of 300 °C–600 °C was developed to activate hydrogen peroxide (H₂O₂) for the efficient degradation of ethylbenzene in aqueous solution. It was revealed that the degradation efficiency of ethylbenzene and TOC removal were 96.9% and 36.2% respectively after the reaction for 40 min in the presence of initial concentration of 0.1 mmol L⁻¹ ethylbenzene, 2.76 g L⁻¹ nFe₃O₄/BC₅₀₀ with the mass ratio of nFe₃O₄ to BC₅₀₀ of 4:1 and 2.0 mmol L⁻¹ H₂O₂ at pH 7.0. Based on electron paramagnetic resonance (EPR), quenching experiment and X-ray photoelectron spectroscopy (XPS) data, both OH and O₂⁻ radicals were generated in the nFe₃O₄/BC₅₀₀ activated H₂O₂ system, and the OH radicals were the predominant species for the degradation of ethylbenzene. Through electron transfer process, mechanisms of Fe(II), phenolic hydroxyl group and persistent free radicals (PFRs) on BC surfaces accounted for the generation of OH radicals, and Fe(III) in nFe₃O₄ and formed from Fe(II) oxidation responsible for the generation of O₂⁻ radicals in the nFe₃O₄/BC activated H₂O₂ system were proposed.

The effect of relative humidity and temperature on the submicron aerosol variability and its ageing process was studied over a high altitude site, Mahabaleshwar in south-west India. The mass composition of non-refractory particulate matter of 1 μm (NR-PM₁) size was obtained using Time of Flight Aerosol Chemical Speciation Monitor (ToF-ACSM) along with the measurements on a few trace gases during winter (December 2017–February 2018) and summer season (20th March - 5th May 2018). Sulfate exhibited strong dependence on the relative humidity (RH) as its mass fraction increased with the increase in RH. The Sulfate oxidation ratio (SOR) calculated during summer season also showed an increasing trend with RH indicating the influence of aqueous phase oxidation on sulfate fraction. On the other hand, OOA showed remarkable enhancement in its mass fraction with the increase in temperature along with the corresponding increase in f₄₄ and tropospheric ozone. OOA, ozone and f₄₄ ratio increased 14–34%, 8–26% and 25–43% respectively with the increase in temperature from 18 to 30 °C. This is indicative of the dominance of photochemical ageing processes during high temperature conditions. The extent of photochemical ageing was found to be higher during summer season (mean temperature ∼25.4 ± 2.6 °C) as compared to winter season (mean temperature ∼20.5 ± 2.6 °C). The nitrate diurnal was majorly governed by gas to particle partitioning process during winter season, whereas the summertime nitrate diurnal was influenced primarily by its formation rate. The non parametric wind regression analysis revealed that the mass concentration during winter was majorly contributed by distant sources from north east direction while during summer the local sources were more dominant.

Pine needles are employed as alternative biomonitoring agents in atmospheric studies. In this study, pine (Pinus Pinea) components (needles and branches) and air samples were collected simultaneously to monitor polychlorinated biphenyls (PCBs), polycyclic aromatic hydrocarbons (PAHs) and organochlorine pesticides (OCPs) from Gemlik, Turkey between January and December 2016. The relationship between ambient air and pine needles were examined to enlighten the usability of pine components as passive samplers for persistent organic pollutants (POPs) in the Marmara region. Average ∑14PAH concentrations for the ambient air, pine needles, and pine branches were 23.1 ± 18.3 ng/m3, 626 ± 306 ng/g DW and 548 ± 261 ng/g DW respectively. PCB concentrations were 118 ± 74 pg/m3, 7.5 ± 2.1 ng/g DW and 6.8 ± 2.9 ng/g DW and ∑10 OCP concentrations were 122 ± 89 ng/m3,1.3 ± 1.5 ng/g DW and 10.0 ± 3.8 ng/g DW in the same order. Levels of PAHs and PCBs were higher in needles than branches. PAH, PCB and OCP concentrations in pine components tended to decrease with increasing temperatures in spring. PAH compounds with medium and light molecular weighted ones were found to be dominant. On the other hand, the predominant PCB components were the medium-weighted congeners while γ-HCH, Heptachlor endo. Epox. Iso A, endrin aldehyde, and methoxychlor were the dominant OCP species.