Selenium (Se) is both an essential micronutrient and a contaminant of concern that is of particular interest in mining-influenced waterbodies in Canada. The objective of this research was to characterize the trophic dynamics of selenium along a gradient of exposure concentrations in a Canadian boreal lake ecosystem. From June 20 to August 22, 2018, six limnocorrals (littoral, ∼3000 L enclosures) were spiked with mean measured concentrations of 0.4, 0.8, 1.6, 3.4, 5.6 and 7.9 μg Se/L as selenite, and three limnocorrals served as untreated controls (background aqueous Se = 0.08–0.09 μg/L). Total Se (TSe) concentrations in water, periphyton, phytoplankton, sediment, benthic macroinvertebrates, zooplankton and female finescale dace (Phoxinus neogaeus; added on day 21 of the experiment) were measured throughout and at the end of the experiment. Total Se bioaccumulation by organisms was generally non-linear. Greater uptake by phytoplankton than periphyton was observed. Taxonomic differences in accumulation of TSe by invertebrates (Heptageniidae = Chironomidae > zooplankton) were observed as well. Fish muscle and ovary tissue TSe bioaccumulation was more variable than that at lower trophic levels and uptake patterns indicated that fish did not reach steady state concentrations. This research provides field-derived models for the uptake of Se by algae and invertebrates, and contributes to a better understanding of the dynamics of TSe bioaccumulation over a gradient of exposure concentrations in cold-water lentic systems.

Scleractinian coral are experiencing global and regional stressors. Microplastics (<5 mm) are an additional stressor that may cause adverse effects on coral. Experiments were conducted to investigate ingestion size limits and retention times of microspheres in a two-day exposure as well as observing growth responses in a 12-week exposure in two Atlantic species, Pseudodiploria clivosa and Acropora cervicornis. In the two-day exposure, P. clivosa ingested a higher number of microspheres ranging in size from 425 μm–2.8 mm than A. cervicornis. Both species egested the majority of microspheres within 48 h of ingestion. In the long-term exposure, calcification and tissue surface area were negatively affected in the treatment group of both species. Exposure also negatively affected buoyant weight in A. cervicornis but not in P. clivosa. The results indicate that microplastics can affect growth responses, yet additional research is warranted to investigate potential synergistic impacts of microplastics and other stressors.

While local anthropogenic emission sources contribute largely to deteriorate metro air quality, long range transport can also play a significant role in influencing levels of pollutants, particularly carbon monoxide (CO) that has a relatively long life span. A nationwide lockdown of two months imposed across India amid COVID-19 led to a dramatic decline in major sources of emissions except for household, mainly from cooking. This initially led to declined levels of CO in two of the largest megacities of India, Delhi and Mumbai under stable weather conditions, followed by a distinctly different variability under the influence of prevailing mesoscale circulation. We hereby trace the sources of CO from local emissions to transport pathways and interpret the observed variability in CO using the interactive WRF-Chem model and back trajectory analysis. For this purpose, COVID-19 emission inventory of CO has been estimated. Model results indicate a significant contribution from externally generated CO in Delhi from surrounding regions and an unusual peak on 17th May amid lockdown due to long range transport from the source region of biofuel emissions in central India. However, the oceanic winds played a larger role in keeping CO levels in check in a coastal megacity Mumbai which otherwise has high CO emissions from household sources due to a larger share of urban slums. Keeping track of evolving carbon-intensive pathways can help inform government responses to the COVID-19 pandemic to prioritize controls of emissions sources.

To characterize the emissions of polycyclic aromatic hydrocarbons (PAHs) from residential biomass burning and coal combustion in field environments, smoke samples were collected from the combustion of six types of biomass in heated kangs and four types of coal in traditional stoves and semi-gasifier stoves. The emission factors (EFs) of the total PAH were in the range of 84.5–344 mg/kg for biomass burning, with lower EFs for biomass with higher densities, and in the range of 38.0–206 mg/kg for coal combustion, with lower EFs for coals with higher maturity. Moreover, EFs were lower from high-density biomass fuels (wood trunk, 84.5 ± 11.3 mg/kg) than low-maturity coals (bituminous coal, 206 ± 16.5 mg/kg). Parent, oxygenated, alkylated, and nitrated PAHs accounted for 81.1%, 12.6%, 6.2%, and 0.1%, respectively, of the total-PAH EFs from biomass burning, and 84.7%, 13.8%, 1.4%, and 0.1%, respectively, of the total-PAH EFs from coal combustion. PAH source profiles differed negligibly between biomass fuels but differed significantly between bituminous coal and anthracite coal fuels. The characteristic species of sources were phenanthrene, 9-fluorenone, and 2-nitrobiphenyl for biomass burning, and were phenanthrene, benzo[ghi]perylene, 1,4-naphthoquinone, and 2-nitrobiphenyl for coal combustion. The ratios of benzo[b]fluoranthene/(benzo[b]fluoranthene + benzo[k]fluoranthene) were 0.40–0.45 for biomass burning and 0.89–0.91 for coal combustion, and these significantly different values constitute unique markers for distinguishing these fuels in source apportionment. Benzo[a]pyrene-equivalent factor emissions were 2.79–11.3 mg/kg for biomass and 7.49–41.9 mg/kg for coal, where parent PAHs contributed 92.0%–95.1% from biomass burning and 98.6%–98.8% from coal combustion. Total-PAH emissions from residential heating were 1552 t across Shaanxi province, to which wheat straw (445 t) in biomass burning and bituminous coal (438 t) in coal combustion were the highest contributors. Results from this study provide crucial knowledge for the source identification of PAHs as well as for the design of abatement strategies against pollutant emissions.

The overnight stagnation of tap water in plumbing systems can lead to water quality deterioration. Meanwhile, the indoor heating can improve the indoor temperature in cold areas during winter, which may affect the quality of tap water during stagnation. However, indoor heating drives bacterial ecological links with tap water stagnation during winter are not well understood. The results indicated that the water temperature increased significantly after stagnation during indoor heating periods. Moreover, the average intact cell number and total adenosine triphosphate (ATP) concentration increased 1.53-fold and 1.35-fold after stagnation, respectively (P < 0.01). In addition, the increase in the ATP per cell number indicated that the combined effects of stagnation and indoor heating could enhance the bacterial activity. Biolog data showed that the bacterial community metabolic capacity was significantly higher in stagnant water than that of fresh water. Co-occurrence networks suggested that the bacterial metabolic profile changed after stagnation during the heating periods. DNA analysis indicated that the composition of the bacterial community changed dramatically after stagnation. The abundances of potential pathogens such as Mycobacterium sp. and Pseudomonas sp. also increased after stagnation. These results will give novel insights on comprehensive understanding the combined effects of indoor heating and overnight stagnation on the water bacterial community ecology of plumbing systems, and provide a scientific basis for tap water quality management after overnight stagnation during the indoor heating periods.

Accumulating evidences indicated that heavy metals may disrupt human sex hormones. However, the combined effects of heavy metals on sex hormones remain to be clarified. To explore the independent and combined associations between heavy metal exposure and serum sex hormones among adults, data of 2728 adults from the National Health and Nutrition Examination Survey (NHANES) was applied. We examined independent and combined associations of fourteen urinary heavy metals and three serum sex steroid hormones (total testosterone (TT), estradiol (E2) and sex hormone-binding globulin (SHBG)). Multivariate linear regression was used to evaluate the independent associations between metal exposure and sex hormone alterations. Principle component analysis -weighted quantile sum regression (PCA-WQSR) model was performed to estimate the combined associations in our individuals. In the co-exposure model, we determined that weighted quantile sum (WQS) index of industrial pollutants was negatively associated with E2 in females (WQS Percent change₈₋ₘₑₜₐₗ = -20.6%; 95% CI: -30.1%, -9.96%), while in males WQS index of water pollutants was negatively related to SHBG (WQS Percent change₈₋ₘₑₜₐₗ = -5.35%; 95% CI: -9.88%, -0.598%). Cadmium (Cd), tin (Sn) and lead (Pb) were the dominating metals of female E2-negative association while Ba was the leading contributor related to male SHBG reduction, which was consistent with the results of multivariate linear regression. Additionally, in postmenopausal women, the associations of E2 decrease with heavy metal co-exposure remained significant while Cd and monomethylarsonic acid (MMA) were identified as hazardous metals in the mixture. We concluded that the exposure to heavy metals was associated with human sex hormone alterations in independent or combined manners. Considering the design of NHANES study, further studies from other national-representative surveys are necessary.

Ground level ozone exerts a strong impact on crop yields, yet how to properly quantify ozone induced yield losses in China remains challenging. To this end, we employed a series of O₃-crop models to estimate ozone induced yield losses in China from 2014 to 2018. The outputs from all models suggested that the total Relative Yield Losses (RYL) of wheat in China from 2014 to 2018 was 18.4%–49.3% and the total RYL of rice was 6.2%–52.9%. Consequently, the total Crop Production Losses (CPL) of wheat and rice could reach 63.9–130.4 and 28.3–35.4 million tons, and the corresponding Total Economic Losses (TEL) could reach 20.5–44.7 and 11.0–15.3 billion dollars, stressing the great importance and urgency of national ozone management. Meanwhile, the estimation outputs highlighted the large variations between different regional O₃-crop models when applying to large scales.Instead of applying one unified O₃-crop models to all regions across China, we also explored the strategy of employing specific O₃-crop models in corresponding (and neighboring) regions to estimate ozone induced yield loss in China. The comparison of two strategies suggested that the mean value from multiple models may still present an inconsistent over/underestimation trend for different crops. Therefore, it is a preferable strategy to employ corresponding O₃-crop models in different regions for estimating the national crop losses caused by ozone pollution. However, the severe lack of regional O₃-crop models in most regions across China makes a robust estimation of national yield losses highly challenging. Given the large variations between O₃-crop interactions across regions, a systematic framework with massive regional O₃-crop models should be properly designed and implemented.

Urban black-odor water (BOW) is a typical phenomenon seen in the urban water environment; it is caused by excessive pollution by organic matter and other pollutants, such as nitrogen and phosphorous. Chromophoric dissolved organic matter (CDOM) is a major optical fraction of dissolved organic matter. In this study, optical properties and components of CDOM were obtained from 178 river samples collected from five cities in China, the sample were investigated using absorption and fluorescence spectroscopy. The collected included 89 ordinary water (OW) samples, 63 mild BOW (MBOW), and 26 heavy BOW (HBOW) samples. Significant differences were found in the absorption spectra of the HBOW, MBOW, and OW samples, particularly in their optical parameters (the slope of the spectrum (S₂₇₅₋₂₉₅), and the ratio of two absorption coefficients of CDOM (E₂:E₃)). Additionally, the fluorescence intensity of the humic acid-like component (F₅) and soluble microbial by product-like component (F₄) obtained via the fluorescence regional integration (FRI) method were 3 and 4.2 times higher in HBOW than in OW, respectively; this could be used as an indicator to distinguish OW from BOW in urban rivers. The results obtained using the redundancy method and the strong negative correlation between F₄ and dissolved oxygen (DO) (r = − 0.56) suggested that the composition of CDOM could change significantly under different urban water environments (p < 0.01). Different correlations were also found between F₅, and a355, E₂:E₃, S₂₇₅₋₂₉₅ in different BOW levels, suggesting that the optical parameters of CDOM were mainly determined by the polluted organic matter originating from terrestrial sources with large molecular humic acid-like compounds; optical parameter a355 could distinguish BOW from OW. These findings are conducive in understanding the dynamics of organic matter pollution and to discover the composition and optical properties of the CDOM in urban BOW and OW, thereby providing an effective method for tracking the spatial characteristics of BOW in urban rivers using remote sensing technologies in areas with multiple sources of pollution.

The co-existence of heavy metals and organic compounds including Cr(VI) and p-cresol (pC) in water environment becoming a challenge in the treatment processes. Herein, the synchronous photocatalytic reduction of Cr(VI) and oxidation of pC by silver oxide decorated on fibrous silica zirconia (AgO/FSZr) was reported. In this study, the catalysts were successfully developed using microemulsion and electrochemical techniques with various AgO loading (1, 5 and 10 wt%) and presented as 1, 5 and 10-AgO/FSZr. Catalytic activity was tested towards simultaneous photoredox of hexavalent chromium and p-cresol (Cr(VI)/pC) and was ranked as followed: 5-AgO/FSZr (96/78%) > 10-AgO/FSZr (87/61%) > 1-AgO/FSZr (47/24%) > FSZr (34/20%). The highest photocatalytic activity of 5-AgO/FSZr was established due to the strong interaction between FSZr and AgO and the lowest band gap energy, which resulted in less electron-hole recombination and further enhanced the photoredox activity. Cr(VI) ions act as a bridge between the positive charge of catalyst and cationic pC in pH 1 solution which can improve the photocatalytic reduction and oxidation of Cr(VI) and pC, respectively. The scavenger experiments further confirmed that the photogenerated electrons (e⁻) act as the main species for Cr(VI) to be reduced to Cr(III) while holes (h⁺) and hydroxyl radicals are domain for photooxidation of pC. The 5-AgO/FSZr was stable after 5 cycles of reaction, suggesting its potential for removal of Cr(VI) and pC simultaneously in the chemical industries.