When applied to agricultural soils, phosphate fertilizers and the mineral or organic compounds present in solid and/or liquid waste may raise phosphorus (P) content and increase soil P saturation. The degree of phosphorus saturation (DPS) is a good indicator of potential P loss from agricultural soils. The purpose of this study was to calculate the DPS of samples from an Oxisol amended for 5 years with biosolids and mineral fertilizer. DPS was calculated based on P, iron, and aluminum extracted by ammonium oxalate and oxalic acid (DPSₒₓ) or by Mehlich-1 solution (DPSM₁). Treatments included NPK mineral fertilization (175 kg ha⁻¹of P), B1 = 19.02 t ha⁻¹of biosolids (350 kg ha⁻¹of P), B2 = 38.17 t ha⁻¹of biosolids (703 kg ha⁻¹of P), B3 = 76.26 t ha–¹of biosolids (1,405 kg ha⁻¹of P), and a control (no P added). Water-extractable P (WEP) was also measured. Critical levels of DPSₒₓand DPSM₁(21 and 24 %, respectively) were only achieved in the topsoil (0–0.1 m) at the highest biosolid dose. Concentration of WEP was positively correlated to DPSₒₓand DPSM₁. The DPSM₁method may be an alternative to DPSₒₓfor assessing the environmental risk of P loss from soil into surface runoff.

Quantifying source apportionments of nutrient load and their variations among seasons and hydrological years can provide useful information for watershed nutrient load reduction programs. There are large seasonal and inter-annual variations in nutrient loads and their sources in semi-arid watersheds that have a monsoon climate. The Generalized Watershed Loading Function model was used to simulate monthly nutrient loads from 2004 to 2011 in the Liu River watershed, Northern China. Model results were used to investigate nutrient load contributions from different sources, temporal variations of source apportionments and the differences in the behavior of total nitrogen (TN) and total phosphorus (TP). Examination of source apportionments for different seasons showed that point sources were the main source of TN and TP in the non-flood season, whereas contributions from diffuse sources, such as rural runoff, soil erosion, and urban areas, were much higher in the flood season. Furthermore, results for three typical hydrological years showed that the contribution ratios of nutrient loads from point sources increased as streamflow decreased, while contribution ratios from rural runoff and urban area increased as streamflow increased. Further, there were significant differences between TN and TP sources on different time scales. Our findings suggest that priority actions and management measures should be changed for different time periods and hydrological conditions, and that different strategies should be used to reduce loads of nitrogen and phosphorus effectively.

Understanding oxygen release by plants is important to the design of constructed wetlands for wastewater treatment. Lab-scale systems planted with Phragmites australis were studied to evaluate the amount of oxygen release by plants using electrode techniques and oxygen consumption model. Oxygen release rate (0.14 g O₂/m²/day) measured using electrode techniques was much lower than that (3.94–25.20 gO₂/m²/day) calculated using the oxygen consumption model. The results revealed that oxygen release by plants was significantly influenced by the oxygen demand for the degradation of pollutants, and the oxygen release rate increased with the rising of the concentration of degradable materials in the solution. The summary of the methods in qualifying oxygen release by wetland plants demonstrated that variations existed among different measuring methods and even in the same measuring approach. The results would be helpful for understanding the contribution of plants in constructed wetlands toward actual wastewater treatment.

The concentrations of O₃are increasing, which may have potential adverse effects on crop yield. This paper deals with assessing the intraspecific variability of two wheat cultivars (PBW 343 and M 533) at different growth stages using open top chambers. Mean O₃concentrations were 50.2 and 53.2 ppb, and AOT40 values were 9 and 12.1 ppm h, respectively, in 2008–2009 and 2009–2010. Reproductive stage showed higher AOT40 values (6.9 and 9.2 ppm h) compared to vegetative (2.23 and 2.9 ppm h). Critical levels of a 3-month AOT 40 of 3 ppm h led to 6 % yield reduction in two wheat cultivars for two consecutive years. Variations in photosynthesis rate, stomatal conductance (gₛ), Fv/Fm ratio, photosynthetic pigments, primary and secondary metabolites, morphological parameters, and yield attributes were measured at vegetative and reproductive stages. Reductions in number of leaves, leaf area, total biomass, root/shoot ratio, RGR, photosynthetic pigments, protein content, and Fv/Fm ratio in PBW 343 were more than M 533 at reproductive stage. Photosynthetic rate did not vary between the cultivars, but gₛwas higher in PBW 343 compared to M 533 under ambient O₃. Higher total phenolics and peroxidase activity were recorded in M 533 at reproductive stage conferring higher resistance at latter age. Results of O₃resistance showed that M 533 was sensitive compared to PBW 343 during vegetative stage but developed more resistance at reproductive stage. PBW 343 with larger leaf area and high gₛis more sensitive than M 533 with smaller leaf area and low gₛ. The study suggests that the sensitivity varied with plant growth stage, and the plant showing higher sensitivity during vegetative period developed more resistance during reproductive period due to higher defense mechanism. Though the yield reductions were same in both cultivars under ambient O₃, the mechanism of acquiring the resistance is different between the cultivars.

As one of the widely used antibiotics in the world, the environmental risks of tylosin (TYL) received more and more attention. In order to assess its environmental fate and ecological effects accurately, it is necessary to understand the sorption properties of TYL on the soils/sediments. The sorption of TYL on goethite at different pH and ionic strength conditions were measured through a series of batch experiments and the sorption data of TYL were fitted by Freundlich and dual-mode sorption models. It was obvious that sorption was strongly dependent on pH and ionic strength. Sorption capacity of TYL increased as the pH increased and ionic strength decreased. The pH and ionic strength-dependent trends might be related with complexation between cationic/neutral TYL species and goethite. The sorption affinity of TYL on goethite decreased as ionic strength increased, which only occurred at higher TYL concentrations, suggested that inner complex might have dominated process at low concentrations and outer complex might occur at higher concentrations of TYL. Spectroscopic evidence indicated that tricarbonylamide and hydroxyl functional groups of TYL might be accounted for the sorption on mineral surfaces. The experimental data of TYL sorption could be fitted by surface complexation model (FITEQL), indicating that ≡FeOH with TYL interaction could be reasonably represented as a complex formation of a monoacid with discrete sites on goethite. The sorption mechanism of TYL might be related with surface complexation, electrostatic repulsion, and H-bounding on goethite. It should be noticed that the heterogeneous of sorption affinity of TYL on goethite at various environment to assess its environment risk.

Total dissolved and particulate mercury (Hg), arsenic (As), and antimony (Sb) mass loads were estimated in different seasons (March and September 2011 and March 2012) in the Paglia River basin (PRB) (central Italy). The Paglia River drains the Mt. Amiata Hg district, one of the largest Hg-rich regions worldwide. Quantification of Hg, As, and Sb mass loads in this watershed allowed (1) identification of the contamination sources, (2) evaluation of the effects of Hg on the environment, and (3) determination of processes affecting Hg transport. The dominant source of Hg in the Paglia River is runoff from Hg mines in the Mt. Amiata region. The maximum Hg mass load was found to be related to runoff from the inactive Abbadia San Salvatore Mine (ASSM), and up to 30 g day⁻¹of Hg, dominantly in the particulate form, was transported both in high and low flow conditions in 2011. In addition, enrichment factors (EFs) calculated for suspended particulate matter (SPM) were similar in different seasons indicating that water discharge controls the quantities of Hg transported in the PRB, and considerable Hg was transported in all seasons studied. Overall, as much as 11 kg of Hg are discharged annually in the PRB and this Hg is transported downstream to the Tiber River, and eventually to the Mediterranean Sea. Similar to Hg, maximum mass loads for As and Sb were found in March 2011, when as much as 190 g day⁻¹each of As and Sb were measured from sites downstream from the ASSM. Therefore, the Paglia River represents a significant source of Hg, Sb, and As to the Mediterranean Sea.

To research the impact of adding sawdust on top phase oil, a sewage sludge and poplar sawdust co-pyrolysis experiment was performed in a fixed bed. Gas chromatography (GC)/mass spectrometry (MS) was used to analyze the component distribution of top phase oil. Higher heating value, viscosity, water content, and pH of the top phase oil product were determined. The highest top phase oil yield (5.13 wt%) was obtained from the mixture containing 15 % poplar sawdust, while the highest oil yield (16.51 wt%) was obtained from 20 % poplar sawdust. Top phase oil collected from the 15 % mixture also has the largest amount of aliphatics and the highest higher heating value (28.6 MJ/kg). Possible reaction pathways were proposed to explain the increase in the types of phenols present in the top phase oil as the proportion of poplar sawdust used in the mixture increased. It can be concluded that synergetic reactions occurred during co-pyrolysis of sewage sludge and poplar sawdust. The results indicate that the high ash content of the sewage sludge may be responsible for the characteristic change in the top phase oil obtained from the mixtures containing different proportions of sewage sludge and poplar sawdust. Consequently, co-pyrolysis of the mixture containing 15 % poplar sawdust can increase the yield and the higher heating value of top phase oil.

Air quality problems caused by atmospheric particulate have drawn broad public concern in the global scope. In the paper, the spatiotemporal distributions of fine particle (PM2.5) and inhalable particle (PM10) concentrations estimated with the artificial neural network (ANN) over China during 2006 to 2010 have been discussed. Most high PM10 concentration appears in Xinjiang, Qinghai, Gansu, Ningxia, Hubei, and parts of Inner Mongolia. The distribution of PM2.5 concentration is consistent with China’s three gradient terrains. The seasonal variations of PM2.5 and PM10 concentrations both indicate that they are higher in north China in spring and winter, lowest in summer. In autumn, most provinces in south China appear high value. In particular, high PM2.5 concentration appears in the southeast coastal cities while high PM10 concentration prefers the central regions in south China. On this basis, seasonal Mann–Kendall test method is utilized to analyze the short-term trends. The results also show significant changes of PM2.5 and PM10 concentrations of China in the past 5 years, and most provinces present the tendency of reduction (3–5 μg/m³for PM2.5 and 10–20 μg/m³for PM10 per year) while a fraction of provinces appear the increasing trend of 8–16 μg/m³(PM2.5) and 16–30 μg/m³(PM10). Simultaneously, PM2.5 population exposure is discussed with the combination of population density-gridded data. Municipalities get much higher exposure level than other provinces. Shanghai suffers the highest population exposure to PM2.5, followed by Beijing and then Tianjin, Jiangsu province. Most provincial capitals, such as Guangzhou, Nanjing, Chengdu, and Wuhan, face much higher exposure level than other regions of their province. Moreover, the PM2.5 exposure situation is more serious in southeast than northwest regions for Beijing-Tianjin-Hebei region. Also, per capita PM2.5 concentration and population-weighted PM2.5 concentration are calculated. The former shows that the high-level regions distribute in Guangdong, Shanghai, and Tianjin, while the latter in Hebei, Chongqing, and Shandong provinces. Further studies may consider optimizing concentration estimation model and use it to discuss the effects of particulate matters on human health.

This paper reports, for the first time, the concentrations of selected phthalates in drinking water consumed in Portugal. The use of bottled water in Portugal has increased in recent years. The main material for bottles is polyethylene terephthalate (PET). Its plasticizer components can contaminate water by leaching, and several scientific studies have evidenced potential health risks of phthalates to humans of all ages. With water being one of the most essential elements to human health and because it is consumed by ingestion, the evaluation of drinking water quality, with respect to phthalate contents, is important. This study tested seven commercial brands of bottled water consumed in Portugal, six PET and one glass (the most consumed) bottled water. Furthermore, tap water from Lisbon and three small neighbor cities was analyzed. Phthalates (di-n-butyl phthalate ester (DnBP), bis(2-ethylhexyl) phthalate ester (DEHP), and di-i-butyl phthalate ester (DIBP)) in water samples were quantified (PET and glass) by means of direct immersion solid-phase microextraction and ionic liquid gas chromatography associated with flame ionization detection or mass spectrometry due to their high boiling points and water solubility. The method utilized in this study showed a linear range for target phthalates between 0.02 and 6.5 μg L⁻¹, good precision and low limits of detection that were between 0.01 and 0.06 μg L⁻¹, and quantitation between 0.04 and 0.19 μg L⁻¹. Only three phthalates were detected in Portuguese drinking waters: dibutyl (DnBP), diisobutyl (DIBP), and di(ethylhexyl) phthalate (DEHP). Concentrations ranged between 0.06 and 6.5 μg L⁻¹for DnBP, between 0.02 and 0.16 μg L⁻¹for DEHP, and between 0.1 and 1.89 μg L⁻¹for DIBP. The concentration of DEHP was found to be up to five times higher in PET than in glass bottled water. Surprisingly, all the three phthalates were detected in glass bottled water with the amount of DnBP being higher (6.5 μg L⁻¹) than in PET bottled water. These concentrations do not represent direct risk to human health. Regarding potable tap water, only DIBP and DEHP were detected. Two of the cities showed concentration of all three phthalates in their water below the limits of detection of the method. All the samples showed phthalate concentrations below 6 μg L⁻¹, the maximum admissible concentration in water established by the US Environmental Protection Agency. The concentrations measured in Portuguese bottled waters do not represent any risk for adult's health.

The use of pesticides to increase agricultural production can result in the contamination of the environment, causing changes in the genetic structure of organisms and in the loss of biodiversity. This practice is also inducing changes in the rainforest ecosystem. In this work, a Pseudomonas aeruginosa isolated from a preservation soil area of the Brazilian Amazon Forest, without usage of any pesticide, was evaluated for its potential to degrade atrazine. This isolate presented all responsible genes (atzA, atzB, atzC, atzD, atzE, and atzF) for atrazine mineralization and demonstrated capacity to use atrazine as a nitrogen source, having achieved a reduction of 44 % of the initial concentration of atrazine after 24 h. These results confirm gene dispersion and/or a possible contamination of the area with the herbicide, which reinforces global concern of the increase and intensive use of pesticides worldwide.