Due to ever-increasing state and federal regulations, the future use of fumigants is predicted on reducing negative environmental impacts while offering sufficient pestcontrol efficacy. To foster the development of a best management practice, an integrated tool is needed to simultaneously predict fumigant movement and pest control without having to conduct elaborate and costly experiments. The objective of this study was (i) to present a two-dimensional (2-D) mathematical model to describe both fumigant movement and pestcontrol and (ii) to evaluate the model by comparing the simulated and observed results. Both analytical and numerical methods were used to predict methyl iodide (MeI) transport and fate. To predict pest control efficacy, the concentration-time index (CT) was defined and a two-parameter logistic survival model was used. Dose-response curves were experimentally determined for MeI against three types of pests (barnyardgrass [Echinochloa crus-galli] seed, citrus nematode [Tylenchulus semipenetrans], and fungi [Fusarium oxysporum]). Methyl iodide transport and pest control measurements collected from a 2-D experiimental system (60 by 60 cm) were used to test the model. Methyl iodide volatilization rates and soil gas-phase concentrations over time were accurately simulated by the model. The mass balance analysis indicates that the fraction of MeI degrading in the soil was underestimated when determined by the appearance of iodide concentration. The experimental results showed that after 24 h of MeI fumigation in the 2-D soil chamber, fungal population was not suppressed; > 90% of citrus nematodes were killed; and barnyardgrass seeds within 20-cm distance from the center were affected. These experimental results were consistent with the predicted results. The model accurately estimated the MeI movement and control of various pests and is a powerful tool to evaluate pesticides in terms of their negative environmental impacts and pest control under various environmental conditions and application methods. 相似文献
Rhodamine B can be degraded using Prussian blue as a photo-Fenton like reagent under λ > 420 nm visible irradiation. Kinetic
studies show ln(Co/Ct) is linearly proportional to the reaction time during the photo-degradation process; thus, the degradation reaction obeys
a pseudo-first order kinetic law. It is very interesting that the presence of salinity such as 0.1 M KCl can speed up greatly
the degradation rate: the time to achieve 90.0% degradation ratio is shortened from 120.0 to 40.0 min under comparable conditions,
which is very useful in the treatment of wastewaters with high content of salinity. 相似文献
Understanding ozone (O3) formation regime is a prerequisite in formulating an effective O3 pollution control strategy. Photochemical indicator is a simple and direct method in identifying O3 formation regimes. Most used indicators are derived from observations, whereas the role of atmospheric oxidation is not in consideration, which is the core driver of O3 formation. Thus, it may impact accuracy in signaling O3 formation regimes. In this study, an advanced three-dimensional numerical modeling system was used to investigate the relationship between atmospheric oxidation and O3 formation regimes during a long-lasting O3 exceedance event in September 2017 over the Pearl River Delta (PRD) of China. We discovered a clear relationship between atmospheric oxidative capacity and O3 formation regime. Over eastern PRD, O3 formation was mainly in a NOx-limited regime when HO2/OH ratio was higher than 11, while in a VOC-limited regime when the ratio was lower than 9.5. Over central and western PRD, an HO2/OH ratio higher than 5 and lower than 2 was indicative of NOx-limited and VOC-limited regime, respectively. Physical contribution, including horizontal transport and vertical transport, may pose uncertainties on the indication of O3 formation regime by HO2/OH ratio. In comparison with other commonly used photochemical indicators, HO2/OH ratio had the best performance in differentiating O3 formation regimes. This study highlighted the necessities in using an atmospheric oxidative capacity-based indicator to infer O3 formation regime, and underscored the importance of characterizing behaviors of radicals to gain insight in atmospheric processes leading to O3 pollution over a photochemically active region. 相似文献
Previous assessments of the effectiveness of protected areas (PAs) focused primarily on changes in human pressure over time and did not consider the different human-pressure baselines of PAs, thereby potentially over- or underestimating PA effectiveness. We developed a framework that considers both human-pressure baseline and change in human pressure over time and assessed the effectiveness of 338 PAs in China from 2010 to 2020. The initial state of human pressure on PAs was taken as the baseline, and changes in human pressure index (HPI) were further analyzed under different baselines. We used the random forest models to identify the management measures that most improved effectiveness in resisting human pressure for the PAs with different baselines. Finally, the relationships between the changes in the HPI and the changes in natural ecosystems in PAs were analyzed with different baselines. Of PAs with low HPI baselines, medium HPI baselines, and high HPI baselines, 76.92% (n=150), 11.11% (n=12), and 22.86% (n=8) , respectively, showed positive effects in resisting human pressure. Overall, ignoring human-pressure baselines somewhat underestimated the positive effects of PAs, especially for those with low initial human pressure. For PAs with different initial human pressures, different management measures should be taken to improve effectiveness and reduce threats to natural ecosystems. We believe our framework is useful for assessing the effectiveness of PAs globally, and we recommend it be included in the Convention on Biological Diversity Post-2020 Strategy. 相似文献
Water contamination by emerging organic pollutants is calling for advanced methods of remediation such as iron-activated sulfite-based advanced oxidation. Sulfate radical, SO4??, and hydroxyl radical, ?OH, are the primary reactive intermediates formed in the Fe(III)/sulfite system, yet the possible involvement of Fe(IV) produced from Fe(II) and persulfates is unclear. Here we explored the role of Fe(IV) in the Fe(III)/sulfite system by methyl phenyl sulfoxide (PMSO) probe assay, electron paramagnetic resonance spectra analysis, alcohol scavenging experiment, and kinetic simulation. Results show that PMSO is partially transformed into methyl phenyl sulfone (PMSO2), thus evidencing Fe(IV) formation. The remaining degradation of PMSO is due to SO4?? and ?OH. The contribution of Fe(IV) versus free radicals is progressively promoted when the Fe(III)-sulfite reaction proceeds, with an upper limit of 80–90%. The contribution of Fe(IV) versus free radicals increases with Fe(III) and sulfite dosages, and decreases with increasing pH. Overall, our findings demonstrate the involvement of Fe(IV) in the Fe-catalyzed sulfite auto-oxidation process.