Phosphorus is a dominant environmental factor in fostering eutrophication, and its biogeochemical behavior has attracted much attention. This study investigated the distribution of phosphorus fractions and the adsorption-desorption characteristic in the soils of wetlands converted from paddy fields with a restoration duration of 1, 2, 3, 5, 13, or 19 years. The results demonstrated the content of total phosphorus (TP) first increased, which was then reversed until the process stabilized after 5 restoration years. Labile inorganic phosphorus (L-Pi), labile organic phosphorus (L-Po), iron-aluminum–bound phosphorus (Fe.Al-P), and humic phosphorus (Hu-P) peaked at 1–3 restoration years, respectively, while moderately labile organic phosphorus (Ml-Po), calcium-magnesium–bound phosphorus (Ca.Mg-P), and residual phosphorus (Re-P) decreased within 0–5 restoration years. During the 5th to 19th restoration years, the contents of all phosphorus fractions stabilized within a minor fluctuating range. Redundancy analysis (RDA) results indicated that total nitrogen (TN) and soil organic matter (SOM) are the important environmental factors controlling redistribution of phosphorus fractions. The capability of restored wetlands to retain phosphorus increased first and then decreased with the extension of the restoration duration. Path analysis (PA) results demonstrated that pH, TN, and Fe are the primary factors for the capacity of soil to retain phosphorus, followed by SOM, Mn, and electrical conductivity(EC). Fe.Al-P and Hu-P had a higher release risk with approximate amounts of 197.25–337.25 and 113.28–185.72 mg/kg during the first stage of restoration, which needs to be focused.

A kinetic model describing Fenton and photo-Fenton degradation of paracetamol (PCT) and consumption of hydrogen peroxide (H₂O₂) was proposed. A set of Fenton and photo-Fenton experiments (18 runs in total) was performed by fixing the initial concentration of PCT to 40 mg L⁻¹ and varying the initial concentrations of H₂O₂ and ferrous ion, Fe²⁺. The experimental set-up was a well-stirred annular photoreactor equipped with an actinic BL TL-DK 36 W/10 1SL lamp. Experimental results highlighted that PCT is no more detected by HPLC analysis within a minimum reaction time of 2.5 and a maximum reaction time of 15.0 min. Besides, a maximum conversion of total organic carbon (TOC) of 68.5% was observed after 75 min of reaction in case of using UV radiation and the highest concentrations of the Fenton reagents. The experimental data were used to fit the kinetic model. The radiation field inside the reactor was taken into account through the local volumetric rate of photon absorption, evaluated by assuming a line source model with spherical and isotropic emission. The kinetic parameters were estimated by using a non-linear least-squares regression procedure and root mean square errors (RMSE) were calculated in order to validate the feasibility of the proposed model. A good agreement between experimental and predicted data was observed and the lowest values of RMSE resulted in 5.84 and 9.59% for PCT and H₂O₂ normalized concentrations, respectively.

Two-dimensional HPLC (2D-HPLC) recently has received great attention due to providing high resolving power and higher peak capacities than that of 1D-HPLC, especially dealing with a wide spectrum of sample matrices containing several components. In this work, an on-line heart-cutting two-dimensional liquid chromatography (2D-LC) method was developed using monolithic columns coupled with reversed-phase liquid chromatography (RPLC). 2D-HPLC was successfully carried out using affinity-based monolithic columns at first dimension (20 cm × 4.6 mm I.D.) followed by a Pinnacle II PAH column (50 mm × 4.6 mm I.D.) at the second dimension. Furthermore, good linearity was observed for the correlation of the benzo[a]pyrene (BaP) molecule against the peak areas (R² = 0.994) in the concentration range of 0.01–1.0 ng/mL in 30 min. The limit of detection and the limit of quantification were found to be 4.0 pg/mL and 12.0 pg/mL, respectively. Both the intra-day and inter-day precision at 0.01 and 0.1 ng/mL spiked concentrations were below than 2.35% RSD whereas the means of the recovery data of the BaP from the water samples were found to be in the range of 93.71–98.65%. These results demonstrate that the 2D-HPLC system, developed by the combination of the P(HEMA-MAPA) column and Pinnacle II PAH column, is reliable, stable, and well qualified in the extraction of polycyclic aromatic hydrocarbons from the water samples.

Washing of contaminated soils or sediments using humic substances (HS) extracted either from source-rich materials or compost has been tested effective to remove various heavy metals. Nevertheless, the remaining chemical fractionation of metals and post-washing biological responses were not discussed in previous research. In this study, we used a HS extracted from green waste compost to wash off Cd, As, and Ni from a contaminated sediment, and evaluated the washing effect on sediment microbes by measuring a series of indexes with regard to microbial biomass and enzyme activities. Results showed that HS washing was more effective in removing the cationic metals Cd and Ni than the anionic metal As. The highest HS dose of 2000 mg L⁻¹ resulted in 24.5-, 33.1-, and 12-fold increases of removal for Cd, Ni, and As, respectively. The remaining Cd and As were found to migrate to less stable fractions, whereas the remaining Ni was dominantly found in the residual fraction. Increases of metal removal efficiency, microbial biomass, and dehydrogenase activity were found to correlate with the increase of HS concentrations. Increasing doses of HS slightly altered sediment pH to the lower range but did not cause any significant effect on microbial activities. The study proves that HS washing is indeed a more environmental-friendly strategy than many existing washing agents which have exerted various side effects on soil properties.

Despite the widespread use of the insecticide imidacloprid (IMI), a neonicotinoid, there is an urgent need for documenting information related to its acute toxicity. Therefore, this study aims to explore the markers of IMI acute toxicity in the testes of the red palm weevil (Rhynchophorus ferrugineus). The LC₅₀ of IMI was determined at 15.7 ppm for male R. ferrugineus. We assessed biochemical alterations in the testes resulting from treatment with four IMI concentrations (10, 15, 20, and 30 ppm). A reduction in glutathione content and acetylcholine esterase activity followed the IMI concentration in a dependent manner. Catalase activity was inhibited only at 20 ppm, while it increased significantly at 30 ppm. Lipid peroxidation increased steadily as the IMI concentrations increased. Based on ultrastructural analyses of spermiogenic stages, acute IMI toxicity produced swelling and degeneration of spermatid mitochondria indicating structural imbalances in their membranes. Further, abnormal chromatin condensation in nuclei and even loss of sperm were also apparent. This study provides biochemical and ultrastructural indicators for acute toxicity resulting from IMI.

This study enabled the assessment of indoor CO₂ levels and evaluated the relationship between occupancy numbers with CO₂ levels in a Taiwan hospital. The measurements were conducted over four seasons for five working days (Monday to Friday), with sampling conducted simultaneously from 09:00 am to 5:00 pm and across six locations (for spatial variability): hall (H), registration and cashier (RC), waiting area (WA), occupational therapy room (OT), physical therapy room (PT), and outdoors (O). Based on the analysis, three of the five indoor sampling sites showed significant differences in seasonal CO₂ concentrations (p < 0.0001). Based on our result, the physical therapy room had the highest level of CO₂ concentration that exceeded the IAQ standard in Taiwan Environmental Protection Agency (EPA) in all seasons, in that the number of occupants contributing to nearly 40% of the variation in CO₂ measured. Our results also showed that the indoor/outdoor (I/O) ratios of CO₂ concentration for all locations and seasons exceeded 1 in ~ 100% of those locations. The median I/O ratio at sites WA and OT was 2.37 and 2.08 during four seasons, respectively. The highest median I/O ratio was found at site PT, with a calculated range of 2.69 in spring to 3.90 in fall. The highest correlation of occupancy number and CO₂ concentration also occurred in PT which correlation coefficients were estimated at 0.47, 0.65, 0.63, and 0.40 in spring, summer, fall, and winter. The findings of the present study can be used to understand occupancy number and its effect on CO₂ levels in a hospital environment, as well as the effect of time of day (Monday to Friday) on the number of patients admitted.

Nanofiltration polyamide membranes naturally tend towards biofouling, due to their surface physicochemistries. Nisin, a type of short cationic amphiphilic peptide with antimicrobial properties, has been recognized as a safe antimicrobial for food biopreservation and biomedical applications. This study investigates the impact of nisin on the initial bacterial attachment to membranes, its anti-biofouling properties, and characterizes a non-monotonic correlation between nisin concentration and biofilm inhibition. Nisin was found to inhibit B. subtilis (G+) and P. aeruginosa (G−) attachment to both the nanofiltration membrane and the PES membrane. To determine the mechanism of action, we investigated the polysaccharides, protein, and eDNA as target components. We found that the quantities of polysaccharides and eDNA were significantly changed, resulting in bacterial death and anti-adhesion to membrane. However, there were no discernable impacts on protein. We postulated that nisin could prevent irreversible biofouling by decreasing adhesion, killing bacteria, and reducing biofilm formation. We examined membrane flux behavior through bench-scale cross-flow experiments at a set concentration of nisin (100 μg mL⁻¹), with membrane behavior being confirmed using CLSM images. Results showed that nisin could enhance anti-biofouling properties through both anti-adhesive and anti-bacterial effects, and therefore could be a novel strategy against biofouling of membranes.

In this paper, the application of ultrafiltration (UF) technology to treat cadmium (Cd) pollution in surface waters is investigated. The effect of the UF membrane molecular weight cut-off (MWCO), Cd ion (Cd²⁺) concentration, solution pH and ionic strength on the removal, and mass balance of Cd were explored. In addition, the effect of the solution pH on UF membrane fouling was analyzed. The results indicated that UF membranes with a low MWCO resulted in an improved Cd removal rate. In addition, as the Cd²⁺ concentration in feedwater increased, the Cd removal rate decreased, while the Cd concentration in the permeate increased. Since the solution pH and ionic strength had a notable impact on the Cd removal rate, a high pH value and low ionic strength led to a higher removal rate of Cd. Under optimal Cd removal conditions, UF reduced the influent Cd concentration from 1.0 to 0.019 mg/L. For membrane fouling, increasing the solution pH led to more serious membrane fouling. This phenomenon was the result of Cd²⁺ reacting with OH⁻ and forming a Cd (OH)₂ precipitate. The precipitate and humic acid formed compact cakes on the membrane surface and blocked membrane pores. These results provided adequate evidence for the higher removal of Cd with increasing solution pH. In addition, SEM images under different pH conditions were in agreement with the conclusion mentioned above, which provided further support for the effect of the solution pH on Cd removal and membrane fouling.

Malva sylvestris L. is a widely consumed edible-medicinal plant growing all around the world. The aim of our study was the determination of the concentration levels of heavy metals in M. sylvestris L. samples and their extracts from polluted and non-polluted locations in Niš, Republic of Serbia. The analysis of heavy metals was performed by the AAS (Atomic Absorption Spectroscopy) method from soil, plants, and extracts. The heavy metals content (Fe, Cu, Mn, Ni, Pb, Zn, and Cd) in the soil and plants from the contaminated site is increased, but the coefficients of metal uptake are not significantly different in plants from polluted and non-polluted areas. The highest content of metals was found in aqueous, then water-alcoholic, and the smallest content was determined in alcoholic solutions. The content of the tested metals is within the limits recommended by international organizations, so the plant and its extracts can be safely used.

The objective of this study was to investigate whether δ¹³C values can be used to identify pollen specie in the atmosphere. A Burkard 7-day recording volumetric spore trap was used to collected pollens in the atmosphere in Tainan City, Taiwan, from January 2 to December 28, 2006, and a light microscope was used to identify the pollen species and concentrations. A Burkard cyclone sampler was used to collect particulate matter and an elemental analyzer with an isotope ratio mass spectrometer was used to analyze the δ¹³C values. Our data showed that the predominate pollen specie in the atmosphere was Broussonetia papyrifera pollen and that the annual average concentration was 27 grains/m³ (pollen season, 36; nonpollen season, 9 grains/m³). The average δ¹³C value was − 26.19‰ for particulate matter in the atmosphere (pollen season, − 26.00‰; nonpollen season, − 26.28‰). No significant association was observed between δ¹³C values and Broussonetia papyrifera pollen concentrations. However, the δ¹³C value in the atmosphere was associated with the levels of Broussonetia papyrifera pollen among the samples with a diameter of particulate matter smaller than 10 μm at a level lower than 40 μg/m³. In addition, the relative contribution of Broussonetia papyrifera pollen to the carbon in the atmosphere using a two end-member mixing models was found to be associated with the Broussonetia papyrifera pollen concentration. In summary, our study suggested that δ¹³C values can be applied in the assessment of Broussonetia papyrifera pollen specie under specific conditions in the atmosphere.