This study presents levels of ¹³⁷Cs and ⁴⁰K concentrations in the placentas of seals gathered in the period 2007–2015. The mean activity of ¹³⁷Cs and ⁴⁰K was 5.49 Bq kg⁻¹w.w. and 136.6 Bq kg⁻¹ ww respectively. Statistically significant correlation was observed between the ¹³⁷Cs activities in placenta and in herring—the staple food for seals. The concentrations of ¹³⁷Cs and ⁴⁰K were also determined in other tissues (muscle, liver, lung, and brain) of wild seals. The concentrations of ¹³⁷Cs were from 2.59 Bq⁻¹ ww (lungs) to 24.3 Bq kg⁻¹ ww (muscles). The transfer factor values for ¹³⁷Cs (seal tissue/fish) ranged from 0.89 to 2.42 in the case of the placentas and from 1.35 to 8.17 in the case of the muscle. For adults seal, the effective dose from ¹³⁷Cs was 2.98 nGy h⁻¹. The mean external radiation dose to pup was 0.77 nGy h⁻¹ from ¹³⁷Cs and 6.69 nGy h⁻¹ from ⁴⁰K.

Chengdu, the capital city of Sichuan Province, is one of the most polluted cities in China. We used single-particle aerosol mass spectrometer to monitor particulate matter pollution in an urban area of Chengdu from December 9, 2015 to January 4, 2016 to determine the characteristics of air pollution during the winter months. The mass concentrations of particulate matter were high during the whole observation period, with mean values for PM₂.₅ and PM₁₀ of 101 ± 60 and 162 ± 99 μg m⁻³, respectively. The particles were clustered into nine distinct particle types: dust (3%), potassium-elemental carbon (KEC) (24%), organic carbon (OC) (12%), combined OC and EC (OCEC) (6%), K-organic nitrogen (KCN) (10%), K-nitrate (KNO₃) (12%), K-sulfate (KSO₄) (18%), K-sulfate and nitrate (KSN) (12%), and metal (3%) particles. Analysis on different types of day showed that: (1) from “excellent” (days with PM₂.₅ lower than 35 μg m⁻³) to “light pollution” (PM₂.₅ between 75 and 115 μg m⁻³) days, local/regional combustion was the major contributor, whereas the aggravation of pollution from light pollution to “heavy pollution” (PM₂.₅ higher than 150 μg m⁻³) days was mainly determined by the combined effect of local/regional combustion and long-distance transport; (2) as the air quality deteriorated, the mixing of sulfate and nitrate in particles increased sharply, especially sulfate; and (3) the relative aerosols acidity increased from excellent to light pollution days, while decreased significantly from light pollution to heavy pollution days. Backward trajectory analysis showed that there were significant differences in PM₂.₅ concentrations and particle compositions between clusters of trajectories, which affected the level and evolution of PM₂.₅ pollution in Chengdu. These results give a deeper understanding of PM₂.₅ pollution in Chengdu and the Sichuan Basin.

In Taiwan, because of the co-use of some irrigation and drainage canals, a portion of industrial wastewater was directly discharged into irrigation canals or even flowed into rivers or wetlands, causing the heavy metal pollution in waters and sediments. Mercury (Hg) contamination in rivers, irrigation canals, and wetlands has been found in Taiwan, but a thorough investigation on the distribution of Hg and methylmercury (MeHg) in these waters and sediments, which may be present in a greater level with elevating total Hg (THg) concentration and markedly impact human health, is still lacking. In this study, surface waters and surface sediments were sampled from five major rivers, two irrigation canals, two reservoirs, and one wetland in Taiwan, and their THg and MeHg concentrations were quantified. Additionally, statistical analysis was carried out to understand the relationship between sediment properties and MeHg levels. The results showed that irrigation canal sediments were relatively more polluted by Hg and the THg concentrations of some sampling points exceeded the upper limit (i.e., 0.87 mg kg⁻¹) of sediment quality index (SQI) for THg promulgated by Taiwan Environmental Protection Administration, which may be attributed to the co-use of irrigation and drainage canals. Furthermore, the MeHg concentration in irrigation canal sediments was the highest; rivers came in second followed by wetlands. In addition, the Siangshan Wetland was analyzed to have the greatest THg and MeHg concentrations in its surface water. Linear regression analysis also indicated that total organic carbon and clay content substantially affected the MeHg production in sediments.

Worldwide, reef building corals are being degraded due to increasing anthropogenic pressure, and as a result, macroalgal cover is being increased. Hence, mechanism of coral–algal interaction, differential coral response to algal overgrowth, is critical from every geographical location to predict future coral dynamics. This paper documents the frequency of coral–algal (Halimeda) interactions, differential coral response to algal interaction. We found difference in susceptibility among coral genera to competitive effects. Out of 970 coral colonies surveyed, 36.7% were in contact with Halimeda sp. Most frequent contact was observed in Porites (57%) followed by Favites 28% (n = 60), Acropora 26% (n = 48), Platygyra 5% (n = 5) and Symphyllia 4.2% (n = 3). Frequent discoloration and tissue loss were only observed in Porites. Continuous monitoring revealed that long-term algal physical contact prevents light required for polyp for photosynthesis and stops coral feeding ability. In this study, we also found mutual exclusion between Halimeda and coral recruit. Out of 180 coral colonies (size class between 5 and 15 cm) comprised of Favites (n = 74), Acropora (n = 20), Favia (n = 79) and Porites (n = 7) surveyed, none of them were found in Halimeda-dominated sites. The documented effects of recruitment exclusion and tissue mortality followed by algal interaction on major reef building corals (Porites) could affect replenishing process and health of the remaining healthy corals in the Palk Bay reef if algal proliferation rate is not controlled through proper management strategies.

As potassium ferrate(VI) is an important kind of water treatment agent which has a high efficiency in algal removal, its effects on the cell substance are rarely discussed. The changing of the protein and enzyme was analyzed here to deeply understand the oxidation of Fe on the protein in the algae. The result of the research showed the inactivation on growth and the biochemical process of the algal cell were all inhibited by Fe, including the function of the photosynthesis system. During the process, SOD (superoxide dismutase), CAT (catalase), POD (peroxidase), and GST (glutathione S-transferase) played cooperative roles to prevent the injury on the cells from destructive oxidation stress. The lipid peroxidation strengthened the defense system. The damage was intensified with the increase of ferrate concentration.

Artisanal and small-scale gold mining (ASGM) accounts for almost half of anthropogenic mercury (Hg) emissions worldwide and causes widespread water pollution. In Indonesia, several studies have identified harmful levels of Hg in areas affected by ASGM. While most of these studies focus on mining areas with thousands of miners, water contamination in smaller ASGM areas is less understood. We evaluated Hg contamination in four ASGM areas in Central Java of varying scale (from 30 to 3000 amalgamator barrels at each area), including Jatiroto, Kebonsari, Gumelar, and Kulon Progo. At each location, we collected water samples along river transects upstream and downstream of ASGM areas during the dry season (June–July 2017). Total Hg (THg) concentrations in stream water increased by orders of magnitude from upstream to downstream of ASGM activities at Jatiroto (1.35–4730 ng/L), with smaller observed increases at the other locations. Dissolved THg concentrations exceeded USEPA criteria for aquatic life (12 ng/L) at two of the four ASGM areas. THg concentrations in tailings exceeded 150,000 ng/L. Notably, THg concentrations in stream water were not directly related to the scale of mining, with Jatiroto having the highest concentrations as second smallest mining areas of the four in this study. Downstream of the mining areas, the fraction of dissolved methyl Hg to dissolved THg reached 20%, indicating that active Hg methylation occurs in the watersheds. Further study is needed to investigate Hg transport in the wet season when rainfall and high stream discharge may mobilize contaminated sediment near mining areas.

Where surface-functionalized engineered nanoparticles (NP) occur in drinking water catchments, understanding their transport within and between environmental compartments such as surface water and groundwater is crucial for risk assessment of drinking water resources. The transport of NP is mainly controlled by (i) their surface properties, (ii) water chemistry, and (iii) surface properties of the stationary phase. Therefore, functionalization of NP surfaces by organic coatings may change their fate in the environment. In laboratory columns, we compared the mobility of CeO₂ NP coated by the synthetic polymer polyacrylic acid (PAA) with CeO₂ NP coated by natural organic matter (NOM) and humic acid (HA), respectively. The effect of ionic strength on transport in sand columns was investigated using deionized (DI) water and natural surface water with 2.2 mM Ca²⁺ (soft) and 4.5 mM Ca²⁺ (hard), respectively. Furthermore, the relevance of these findings was validated in a near-natural bank filtration experiment using HA-CeO₂ NP. PAA-CeO₂ NP were mobile under all tested water conditions, showing a breakthrough of 60% irrespective of the Ca²⁺ concentration. In contrast, NOM-CeO₂ NP showed a lower mobility with a breakthrough of 27% in DI and < 10% in soft surface water. In hard surface water, NOM-CeO₂ NP were completely retained in the first 2 cm of the column. The transport of HA-CeO₂ NP in laboratory columns in soft surface water was lower compared to NOM-CeO₂ NP with a strong accumulation of CeO₂ NP in the first few centimeters of the column. Natural coatings were generally less stabilizing and more susceptible to increasing Ca²⁺ concentrations than the synthetic coating. The outdoor column experiment confirmed the low mobility of HA-CeO₂ NP under more complex environmental conditions. From our experiments, we conclude that the synthetic polymer is more efficient in facilitating NP transport than natural coatings and hence, CeO₂ NP mobility may vary significantly depending on the surface coating.

In this study, the removal of ciprofloxacin hydrochloride (a fluoroquinolone antibiotic) by using various effective adsorbents such as activated carbon, montmorillonite, modified montmorillonite (commercial name Cloisite 20A), and alumina was investigated. Adsorption experiments were performed to determine and compare the adsorption capacities of these adsorbents. The adsorption capacities of adsorbents were examined at different initial concentrations of ciprofloxacin hydrochloride. Activated carbon was found to be having the best adsorption capacity for the removal of ciprofloxacin hydrochloride. For the solution having an initial ciprofloxacin hydrochloride concentration of 4 ppm, the adsorption capacities of adsorbents were obtained as 1.86 mg g⁻¹ for activated carbon, 1.67 mg g⁻¹ for modified montmorillonite, 1.15 mg g⁻¹ for alumina, and 0.60 mg g⁻¹ for montmorillonite. And also, about 92% of the ciprofloxacin hydrochloride was removed from the water using the activated carbon. In addition, Langmuir, Freundlich, and Temkin isotherm models were employed to express the adsorption process. For all adsorbents, Freundlich isotherm model provided best fitting to the experimental data because of very high values of R² (> 0.99). Kinetic models of pseudo-first order, pseudo-second order, Elovich, and Weber-Morris intraparticle diffusion model were utilized to evaluate the experimental adsorption data. Adsorption kinetics data were well represented by pseudo-second order kinetic model with values of R² (> 0.999).

²²²Rn, ²²⁰Rn, and their decay products are significant contributors to background radiation dose. Their concentration level, pertaining exposure, and consequent dose are prime concerns in indoor environments. The present study was performed in 101 dwellings of different villages of Almora district situated in Kumaun hills of Indian Himalayan belt. Measurement of gases and decay products were made in three different types of dwellings (i.e., mud, cemented, and stone with plaster) in three seasons (winter, summer, and rainy). Concentration values for ²²²Rn and EERC were found to be varying in the order of winter > summer > rainy while obtained least in rainy season for the case of ²²⁰Rn and EETC. Concentration values for ²²²Rn and EERC were found to be lesser for cemented houses. Relative standard deviation of concentration values was found to be higher for the rainy season. Yearly averaged concentration values for ²²²Rn, EERC, ²²⁰Rn, and EETC were noted to be higher than the global averages but comparable to some Indian studies. Annual inhalation dose due to ²²²Rn, ²²⁰Rn, and their progeny was found to be 0.55–4.71 mSv/year with an average value of 2.36 ± 0.83 mSv/year. These values were measured for the first time in the study area and provide a link for future studies in the dwellings representing higher concentration values.

Wastewater from a limestone-gypsum wet desulfurization system cannot be directly reused or discharged due to its high suspended matter content and complex water composition. Desulfurization wastewater evaporation in flue gas is an effective way to dispose wastewater. Multicomponent soluble chlorine salts exist in the desulfurization wastewater. During the evaporation, chlorine enters into the flue gas due to volatilization, which accelerates the enrichment rate of the Cl⁻ concentration in the desulfurization slurry and leads to an increase in wastewater production. This study explored the chlorine migration of various chlorine salt solutions and typical desulfurization wastewater at high temperature during the evaporation process of concentrated wastewater by a laboratory-scale tube furnace and a pilot-scale system. Results showed that when NaCl-evaporated substance was heated, the chlorine ion hardly volatilized. For the evaporated substances of CaCl₂ and MgCl₂ solutions, some of the crystal water was lost, and hydrolysis occurred to generate gaseous HCl. NH₄Cl was easily sublimed, and the decomposition temperature was lowest. A pilot study on spray evaporation of desulfurization wastewater in flue gas showed that the particle size of the evaporated product increased and the main particle size was within 2.5–10 μm with increasing flue gas temperature. Increasing the mass ratio of gas to liquid significantly reduced the particle size of the atomized particles, thereby reducing the average particle size of the evaporated particles. The HCl concentration increased with increasing flue gas temperature. When the flue gas temperature was 350 °C, the concentration of HCl was 40 ppm, and the escape rate of chlorine in the desulfurization wastewater was approximately 30% using typical wastewater from a limestone-gypsum wet desulfurization system.