Fluctuation exposure of trace metal copper (Cu) is ubiquitous in aquatic environments. The purpose of this study was to investigate the impacts of chronically pulsed exposure on biodynamics and subcellular partitioning of Cu in freshwater tilapia (Oreochromis mossambicus). Long-term 28-day pulsed Cu exposure experiments were performed to explore subcellular partitioning and toxicokinetics/toxicodynamics of Cu in tilapia. Subcellular partitioning linking with a metal influx scheme was used to estimate detoxification and elimination rates. A biotic ligand model-based damage assessment model was used to take into account environmental effects and biological mechanisms of Cu toxicity. We demonstrated that the probability causing 50% of susceptibility risk in response to pulse Cu exposure in generic Taiwan aquaculture ponds was ~33% of Cu in adverse physiologically associated, metabolically active pool, implicating no significant susceptibility risk for tilapia. We suggest that our integrated ecotoxicological models linking chronic exposure measurements with subcellular partitioning can facilitate a risk assessment framework that provides a predictive tool for preventive susceptibility reduction strategies for freshwater fish exposed to pulse metal stressors.

One of the most serious environmental issues of the present century is metal contamination of the aqueous environment due to the release of metal-containing effluents into the water bodies. Cadmium (Cd) is one of the toxic heavy metals which is not biodegradable thereby causing high risks to animals, plants, and humans. In the present study, potential and feasibility of compost derived from fruits and vegetables for Cd biosorption from aqueous solution were investigated. The batch biosorption experiments were performed to evaluate the effects of Cd concentrations (5, 15, 30, and 60 mg/L), compost biomass (0.5, 1.0, and 1.5 g/100 mL), pH (4, 6, and 8), contact time (1, 4, and 19 h), and temperature (28 and 35 °C) on Cd sorption and removal by compost. The biosorption of Cd was found to be highly dependent on initial Cd concentration, sorbent biomass, pH, contact time, and temperature of aqueous solution. It was observed that Cd sorption by compost was rapid up to 4 h, and then it became slow and stable as the contact time shifted towards equilibrium state (19 h). At equilibrium, the Cd sorption (q = 0.33–5.43 mg/g compost) and removal (45–99%) were observed at pH 6 and temperature 28 °C depending upon Cd concentrations and sorbent biomass in aqueous solution. The equilibrium experimental data were fitted well with Langmuir adsorption isotherm model (q ₘₐₓ = 6.35–7.14 mg/g compost, R ² = 0.77–0.98). FTIR spectrum of the compost indicated the presence of hydroxyl and carboxyl groups, which might be involved in the biosorption of Cd through ion exchange and complexation mechanisms. The optimal environmental conditions (pH 6, sorbent biomass 0.5 g/100 mL, and temperature 28 °C) induced more Cd sorption on compost at equilibrium. Results show compost as a cost-effective adsorbent material having high potential for heavy metal remediation from aqueous solution.

The environmental impacts with regard to agro-based biofuel production have been associated with the impact of greenhouse gas (GHG) emissions. In this study, field GHG emissions during plantation stage of palm oil-based biofuel production associated with land use changes for oil palm plantation development have been evaluated. Three different sites of different land use changes prior to oil palm plantation were chosen; converted land-use (large and small-scales) and logged-over forest. Field sampling for determination of soil N-mineralisation and soil organic carbon (SOC) was undertaken at the sites according to the age of palm, i.e. <5 years (immature), 5–20 and >21 years (mature oil palms). The field data were incorporated into the estimation of nitrous oxide (N₂O) and the resulting CO₂-eq emissions as well as for estimation of carbon stock changes. Irrespective of the land conversion scenarios, the nitrous oxide emissions were found in the range of 6.47–7.78 kg N₂O-N/ha resulting in 498–590 kg CO₂-eq/ha. On the other hand, the conversion of tropical forest into oil palm plantation has resulted in relatively higher GHG emissions (i.e. four times higher and carbon stock reduction by >50%) compared to converted land use (converted rubber plantation) for oil palm development. The conversion from previously rubber plantation into oil palm plantation would increase the carbon savings (20% in increase) thus sustaining the environmental benefits from the palm oil-based biofuel production.

Essential oils (EO) obtained from Xylopia parviflora root bark and Hoslundia opposita leaf via hydro distillation were analysed by GC-MS and evaluated for their insectifugal (repellent) and insecticidal activities against cowpea seed bruchid (Callosbruchus maculatus Fabricius), a cosmopolitan pest of cowpea seeds. X. parviflora was predominated by sesquiterpenes (59.57%), with the main compounds being β-himachalene (22.68%), 1,7,7,Trimethylbicyclo[2.2.1]hept-5-en-2-ol (19.68%), β-elemene (14.41%), 5(1H)-Azulenone, 2,4,6,7,8,8a–hexahydro-3,8-dimethyl-4-(1-methylethylidene)-(85-cis)- (12.38%) and (−)-α-parasinsen (8.34%). The predominant compounds in H. opposita EO were 1,8-cineole (61.15%), followed by α-terpineol (16.81%) and β-phellandrene (13.25%). Percentage repellence at application rates of 0.66–1.32 μl/cm² (46.93–73.07%) was significantly (p < 0.05) higher than that of control (17.73%). RD₅₀ (repellence dose for 50% of treated adults) for H. opposita (0.43 μl/cm²) was not significantly different from the value for X. parviflora (0.60 μl/cm²). Although higher percentage of male mortality than female mortality was observed due to topical application of the EOs, the disparity was not significant. The results of correlation of the chemical groups of the EOs with the insectifugal activity indicate that the observed bioactivity was due to the synergistic effects of the chemical groups. The two EOs are therefore recommended for incorporation into bruchid protection schemes in the tropics.

Nowadays, environment problem has become the international hot issue. Experts and scholars pay more and more attention to the energy efficiency. Unlike most studies, which analyze the changes of TFEE in inter-provincial or regional cities, TFEE is calculated with the ratio of target energy value and actual energy input based on data in cities of prefecture levels, which would be more accurate. Many researches regard TFP as TFEE to do analysis from the provincial perspective. This paper is intended to calculate more reliably by super efficiency DEA, observe the changes of TFEE, and analyze its relation with TFP, and it proves that TFP is not equal to TFEE. Additionally, the internal influences of the TFEE are obtained via the Malmquist index decomposition. The external influences of the TFFE are analyzed afterward based on the Tobit models. Analysis results demonstrate that Heilongjiang has the highest TFEE followed by Jilin, and Liaoning has the lowest TFEE. Eventually, some policy suggestions are proposed for the influences of energy efficiency and study results.

In Brazil, landfills are commonly used as a method for the final disposal of waste that is compliant with the legislation. This technique, however, presents a risk to surface water and groundwater resources, owing to the leakage of metals, anions, and organic compounds. The geochemical monitoring of water resources is therefore extremely important, since the leachate can compromise the quality and use of surface water and groundwater close to landfills. In this paper, the results of analyses of metals, anions, ammonia, and physicochemical parameters were used to identify possible contamination of surface water and groundwater in a landfill area. A statistical multivariate approach was used. The values found for alkali metals, nitrate, and chloride indicate contamination in the regional groundwater and, moreover, surface waters also show variation when compared to the other background points, mainly for ammonia. Thus, the results of this study evidence the landfill leachate influence on the quality of groundwater and surface water in the study area.

Chromium pollution of soil and water is a serious environmental concern due to potential carcinogenicity of hexavalent chromium [Cr(VI)] when ingested. Eucalyptus bark biochar (EBB), a carbonaceous black porous material obtained by pyrolysis of biomass at 500 °C under oxygen-free atmosphere, was used to investigate the removal of aqueous Cr(VI) upon interaction with the EBB, the dominant Cr(VI) removal mechanism(s), and the applicability to treat Cr(VI)-contaminated wastewater. Batch experiments showed complete removal of aqueous Cr(VI) at pH 1–2; sorption was negligible at pH 1, but ~55% of total Cr was sorbed onto the EBB surface at pH 2. Detailed investigations on unreacted and reacted EBB through Fourier transform infrared spectroscopy and X-ray photoelectron spectrometry (XPS) indicate that the carboxylic groups in biochar played a dominant role in Cr(VI) sorption, whereas the phenolic groups were responsible for Cr(VI) reduction. The predominance of sorption–reduction mechanism was confirmed by XPS studies that indicated ~82% as Cr(III) and ~18% as Cr(VI) sorbed on the EBB surface. Significantly, Cr(VI) reduction was also facilitated by dissolved organic matter (DOM) extracted from biochar. This reduction was enhanced by the presence of biochar. Overall, the removal of Cr(VI) in the presence of biochar was affected by sorption due to electrostatic attraction, sorption–reduction mediated by surface organic complexes, and aqueous reduction by DOM. Relative dominance of the aqueous reduction mechanism depended on a critical biochar dosage for a given electrolyte pH and initial Cr(VI) concentration. The low-cost EBB developed here successfully removed all Cr(VI) in chrome tanning acidic wastewater and Cr(VI)-contaminated groundwater after pH adjustment, highlighting its potential applicability in effective Cr(VI) remediation.

The presence of UV quenching compounds in landfill leachate can negatively affect UV disinfection in a wastewater treatment plant when leachate is co-treated. Herein, a microbial fuel cell (MFC) was investigated to remove UV quenchers from a landfill leachate with simultaneous bioelectricity generation. The key operating parameters including hydraulic retention time (HRT), anolyte recirculation rate, and external resistance were systematically studied to maximize energy recovery and UV absorbance reduction. It was found that nearly 50% UV absorbance was reduced under a condition of HRT 40 days, continuous anolyte recirculation, and 10 Ω external resistance. Further analysis showed a total reduction of organics by 75.3%, including the reduction of humic acids, fulvic acids, and hydrophilic fraction concentration as TOC. The MFC consumed 0.056 kWh m⁻³ by its pump system for recirculation and oxygen supply. A reduced HRT of 20 days with periodical anode recirculation (1 hour in every 24 hours) and 39 Ω external resistance (equal to the internal resistance of the MFC) resulted in the highest net energy of 0.123 kWh m⁻³. Granular activated carbon (GAC) was used as an effective post-treatment step and could achieve 89.1% UV absorbance reduction with 40 g L⁻¹. The combined MFC and GAC treatment could reduce 92.9% of the UV absorbance and remove 89.7% of the UV quenchers. The results of this study would encourage further exploration of using MFCs as an energy-efficient method for removing UV quenchers from landfill leachate.

Samples of surface soil from tobacco (Nicotiana tabacum L.) fields were analysed for heavy metals and showed the following concentrations (mean of 246 samples, mg/kg): As, 5.10; Cd, 0.11; Cr, 49.49; Cu, 14.72; Hg, 0.08; Ni, 19.28; Pb. 20.20 and Zn, 30.76. The values of the index of geoaccumulation (I gₑₒ) and of the enrichment factor indicated modest enrichment with As, Cd, Cr, Hg, Ni or Pb. Principal component analysis and cluster analysis correctly allocated each investigated element to its source, whether anthropogenic or natural. The results were consistent with estimated inputs of heavy metals from fertilizers, irrigation water and atmospheric deposition. The variation in the concentrations of As, Cd, Cu, Pb and Zn in the soil was mainly due to long-term agricultural practises, and that of Cr and Ni was mainly due to the soil parent material, whereas the source of Hg was industrial activity, which ultimately led to atmospheric deposition. Atmospheric deposition was the main exogenous source of heavy metals, and fertilizers also played an important role in the accumulation of these elements in soil. Identifying the sources of heavy metals in agricultural soils can serve as a basis for appropriate action to control and reduce the addition of heavy metals to cultivated soils.