The photolysis of nitrous acid (HONO) in the early morning hours is an important source of OH radicals, the most important daytime oxidizing species. Although the importance of this mechanism has been recognized for many years, no accurate quantification of this OH source is available, and the role of HONO photolysis is often underestimated. We present measurements of HONO and its precursor NO 2 by Differential Optical Absorption Spectroscopy (DOAS) during the Berliner Ozonexperiment (BERLIOZ) field campaign in July/August 1998 at Pabstthum near Berlin, Germany. HONO concentrations, formation rates, and simultaneously measured HONO photolysis frequencies are used to calculate the total amount of OH formed by HONO photolysis during a full diurnal cycle. A comparison with the OH formation by photolysis of O 3 and HCHO and by the reaction of alkenes with ozone shows that HONO photolysis contributed up to 20% of the total OH formed in a 24 hour period during this campaign. In the morning hours, HONO photolysis was by far the most important OH source during BERLIOZ.

OH formation by HONO photolysis during the BERLIOZ experiment : Photochemistry experiment in BERLIOZ (PHOEBE)

Applications of in vivo and in vitro solid-phase microextraction techniques in plant analysis: A review.

Biogenic volatile organic compounds (BVOCs), released by practically all plants, have important atmospheric and ecological consequences. Because BVOC-emission measurements are especially tedious, complex and extremely variable between species, two approaches have been used in scientific studies to try to estimate BVOC-emission types and rates from plant species. The first, which has known little success, involves grouping species according to plant-taxonomy criteria (typically, genus and family). The second involves studying the correlation between BVOC content and emission (i.e. how leaf content could be used to estimate emissions). The latter strategy has provided controversial results, partly because BVOCs are amazingly chemically diverse, and, as a result, techniques used to study plant BVOC content, which we review, cannot be equally adequate for all analytes. In order to choose an adequate technique, two patterns must be distinguished. Specifically stored compounds – mainly monoterpenes and sesquiterpenes that dominate the essential oil obtained from a plant – are permanently and massively present in specific storage structures (e.g., secretory cavities, trichomes) of the order of μg/g–mg/g and usually allow emissions to occur during stress periods when terpenes are weakly synthesized. These BVOCs can be studied directly through traditional extraction techniques (e.g., hydrodistillation) and novel techniques (e.g., application of microwaves and ultrasound), and indirectly by trapping techniques involving the collection, within adsorbent material, of BVOCs present in the headspace of a plant. Non-specifically stored compounds (e.g., isoprene, 2-methyl-3-buten-2-ol, and, in species without storage structures, monoterpenes and sesquiterpenes) can only be temporarily accumulated in leaf aqueous and lipid phases in small concentrations of the order of ng/g. As a result, studying their concentration in leaves requires the use of trapping techniques, more sensitive to trace amounts. Unlike for specifically stored BVOCs, knowledge of the concentration of non-specifically stored BVOCs cannot provide any information regarding the emission potential of a species but, instead, provides crucial information to understand why BVOC emissions may be uncoupled from the physiological processes that drive their synthesis. We describe both extracting and trapping techniques and discuss them in terms of the technical choices that may cause losses of thermolabile constituents, chemical transformations, different volatile recoveries and suitability to represent plant content of BVOCs faithfully. The second part of this review addresses technical shortcomings and biological and environmental factors that may alter the correlations between BVOC content and emission from plants.

Extracting and trapping biogenic volatile organic compounds stored in plant species

The volatile composition of different apple varieties of Malus domestica Borkh. species from different geographic regions at Madeira Islands, namely Ponta do Pargo (PP), Porto Santo (PS), and Santo da Serra (SS) was established by headspace solid-phase microextraction (HS-SPME) procedure followed by GC-MS (GC-qMS) analysis. Significant parameters affecting sorption process such as fiber coating, extraction temperature, extraction time, sample amount, dilution factor, ionic strength, and desorption time, were optimized and discussed. The SPME fiber coated with 50/30 microm divinylbenzene/carboxen/PDMS (DVB/CAR/PDMS) afforded highest extraction efficiency of volatile compounds, providing the best sensitivity for the target volatiles, particularly when the samples were extracted at 50 degrees C for 30 min with constant magnetic stirring. A qualitative and semi-quantitative analysis between the investigated apple species has been established. It was possible to identify about 100 of volatile compounds among pulp (46, 45, and 39), peel (64, 60, and 64), and entire fruit (65, 43, and 50) in PP, PS, and SS apples, respectively. Ethyl esters, terpenes, and higher alcohols were found to be the most representative volatiles. Alpha-farnesene, hexan-1-ol and hexyl 2-methylbutyrate were the compounds found in the volatile profile of studied apples with the largest GC area, representing, on average, 24.71, 14.06, and 10.80% of the total volatile fraction from PP, PS, and SS apples. In PP entire apple, the most abundant compounds identified were alpha-farnesene (30.49%), the unknown compound m/z (69, 101, 157) (21.82%) and hexyl acetate (6.57%). Regarding PS entire apple the major compounds were alpha-farnesene (16.87%), estragole (15.43%), hexan-1-ol (10.94), and E-2-hexenal (10.67). Alpha-farnesene (30.3%), hexan-1-ol (18.90%), 2-methylbutanoic acid (4.7%), and pentan-1-ol (4.6%) were also found as SS entire apple volatiles present in a higher relative content. Principal component analysis (PCA) of the results clustered the apples into three groups according to geographic origin. Linear discriminant analysis (LDA) was performed in order to detect the volatile compounds able to differentiate the three kinds of apples investigated. The most important contributions to the differentiation of the PP, PS, and SS apples were ethyl hexanoate, hexyl 2-methylbutyrate, E,E-2,4-heptadienal, p-ethyl styrene, and E-2-hexenal.

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Characterization of volatile substances in apples from Rosaceae family by headspace solid‐phase microextraction followed by GC‐qMS

Although the 2Rs (reduce and reuse) are considered high-priority approaches, there has not been enough quantitative research on effective 2R management. The purpose of this paper is to provide information obtained through the International Workshop in Kyoto, Japan, on 11–13 November 2015, which included invited experts and researchers in several countries who were in charge of 3R policies, and an additional review of 245 previous studies. It was found that, regarding policy development, the decoupling between environmental pressures and economy growth was recognized as an essential step towards a sustainable society. 3R and resource management policies, including waste prevention, will play a crucial role. Approaches using material/substance flow analyses have become sophisticated enough to describe the fate of resources and/or hazardous substances based on human activity and the environment, including the final sink. Life-cycle assessment has also been developed to evaluate waste prevention activities. Regarding target products for waste prevention, food loss is one of the waste fractions with the highest priority because its countermeasures have significant upstream and downstream effects. Persistent organic pollutants and hazardous compounds should also be taken into account in the situation where recycling activities are globally widespread for the promotion of a material-cycling society.

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Waste prevention for sustainable resource and waste management

Toona sinensis (A. Juss.) Roem. belonging to the Toona family was used as one of the traditional Chinese medicines in China. Based on microwave-assisted extraction (MAE) and headspace solid-phase microextraction followed by gas chromatography-mass spectrometry, the volatile compounds of Toona sinensis (A. Juss.) Roem. were determined. Results indicated that the optimum condition of the determination of the volatile compounds in Toona sinensis (A. Juss.) Roem. was achieved with the experimental parameters including fiber coating of PDMS/DVB, microwave power of 400 W and irradiation time of 4 min. Under the optimal conditions, for the first time, 45 volatile compounds were separated and identified from the fresh leaves of Toona sinensis (A. Juss.) Roem. The highest content component of the 45 compounds was trans-Caryophyllene (21.422%). Relative standard deviation (RSD) values <9% showed that the present method has good precision. The experimental results demonstrate that MAE-HS-SPME followed by GC–MS is a simple, time-saving and solvent-free method, and it is a potential analytic tool for the determination of the volatile compounds of TCMs.

Rapid Determination of Volatile Compounds in Toona sinensis (A. Juss.) Roem. by MAE-HS-SPME Followed by GC–MS

Background and Purpose: Microcystin-LR (MC-LR), a common toxic species in contaminated aquatic systems, persists for long periods because of its cyclic structure. Ag3PO4 is an environment-friendly photocatalyst with relatively good degradation capacity for hazardous organic pollutants. This study aimed to investigate the degradation capacity of Ag3PO4 for MC-LR under visible light. Methods: An Ag3PO4 photocatalyst was synthesized by the ion-exchange method and characterized by X-ray diffraction, field-emission scanning electron microscope, and UV-Vis spectrophotometer. MC-LR was quantified in each sample through high-performance liquid chromatograph. The degradation efficiency of MC-LR was affected by initial pH, initial Ag3PO4 concentration, initial MC-LR concentration, and recycle experiments. The degradation intermediates of MC-LR were examined by liquid chromatography-mass spectrometry (LC/MS). Results: The degradation process can be well fitted with the pseudo-first-order kinetic model. The maximum MC-LR degradation rate of 99.98% can be obtained within 5 h under the following optimum conditions: pH of 5.01, Ag3PO4 concentration of 26.67 g/L, and MC-LR concentration of 9.06 mg/L. Nine intermediates were detected and analyzed by LC/ MS. Three main degradation pathways were proposed based on the molecular weight of the intermediates and the reaction mechanism: (1) hydroxylation on the aromatic ring of Adda, (2) hydroxylation on the diene bonds of Adda, and (3) internal interactions on the cyclic structure of MC-LR. Conclusion: Ag3PO4 is a highly efficient catalyst for MC-LR degradation in aqueous solutions.

/pdf/a-novel-photocatalytic-material-for-removing-microcystin-lr-4a56gc4kkp.pdf

A novel photocatalytic material for removing microcystin-LR under visible light irradiation: degradation characteristics and mechanisms.

Kinetic and mechanistic study of microcystin-LR degradation by nitrous acid under ultraviolet irradiation

Increased eutrophication in the recent years has resulted in considerable research focus on identification of methods for preventing cyanobacterial blooms that are rapid and efficient. The objectives of this study were to investigate the effects of dihydroartemisinin and artemether on the growth of Microcystis aeruginosa and to elucidate its mode of action. Variations in cell density, chlorophyll a, soluble protein, malondialdehyde, extracellular alkaline phosphatase activity (APA), and chlorophyll fluorescence parameters (Fv/Fm, ΦPSII, ETR, rapid light curves, fast chlorophyll fluorescence curves on fluorescence intensity, and relative variable fluorescence) were evaluated by lab-cultured experiments. Our results demonstrated that both dihydroartemisinin and artemether inhibited the growth of M.aeruginosa by impairing the photosynthetic center in photosystem II and reducing extracellular APA, with a higher sensitivity exhibited toward artemether. The inhibitory effects of dihydroartemisinin on M.aeruginosa increased with concentration, and the maximum growth inhibitory rate was 42.17% at 24 mg·L-1 after 120h exposure, whereas it was 55.72% at 6 mg·L-1 artemetherafter 120h exposure. Moreover, the chlorophyll fluorescence was significantly inhibited (p<0.05) after 120h exposure to 12 and 24 mg·L-1 dihydroartemisinin. Furthermore, after 120h exposure to 6 mg·L-1 artemether, Fv/Fm, ΦPSII, ETR and rETRmax showed a significant decrease (p<0.01) from initial values of 0.490, 0.516, 17.333, and 104.800, respectively, to 0. One-way analysis of variance showed that 6 mg·L-1 artemether and 24 mg·L-1 dihydroartemisinin had significant inhibitory effects on extracellular APA (p<0.01). The results of this study would be useful to further studies to validate the feasibility of dihydroartemisinin and artemether treatment to inhibit overall cyanobacterial growth in water bodies, before this can be put into practice.

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Effects of Dihydroartemisinin and Artemether on the Growth, Chlorophyll Fluorescence, and Extracellular Alkaline Phosphatase Activity of the Cyanobacterium Microcystis aeruginosa

Shoubing Wang

Papers

Rapid Determination of Volatile Compounds in Toona sinensis (A. Juss.) Roem. by MAE-HS-SPME Followed by GC–MS

A novel photocatalytic material for removing microcystin-LR under visible light irradiation: degradation characteristics and mechanisms.

Kinetic and mechanistic study of microcystin-LR degradation by nitrous acid under ultraviolet irradiation

Effects of Dihydroartemisinin and Artemether on the Growth, Chlorophyll Fluorescence, and Extracellular Alkaline Phosphatase Activity of the Cyanobacterium Microcystis aeruginosa

Transcriptomic analysis dissects the regulatory strategy of toxic cyanobacterium Microcystis aeruginosa under differential nitrogen forms.