Aroma fingerprinting of 26 finger lime (Citrus australasica) cultivars grown in Japan based on peel voc profiles

Odorous organic gas emission characteristics from cooked food wastes during aerobic decomposition

All roads lead to Rome: Towards understanding different avenues of tolerance to huanglongbing in citrus cultivars

Finger lime is receiving growing attention as an ingredient of gastronomic preparations of haute cuisine for its delicious flavor and fragrance and for its appealing aspect. Volatile compounds play a crucial role in determining the organoleptic characteristics of the fruit and its pleasantness for consumers. The aim of the present study was to investigate the volatile profiles by headspace solid phase micro-extraction (HS-SPME) coupled to gas chromatography-mass spectrometry (GC-MS) in the peel and, for the first time, in the pulp of three Australian finger lime cultivars grown in Sicily (southern Italy): Pink Pearl, Sanguinea, and Faustrime, allowing to overall identify 84 volatile organic compounds (VOCs). The analytical data showed that the three cultivars were characterized by distinct volatile chemotypes: limonene/sabinene/bicyclogermacrene in the Pink Pearl, limonene/γ-terpinene/bicyclogermacrene in the Sanguinea, and limonene/β-phellandrene/γ-terpinene in the Faustrime. Moreover, some volatiles, found exclusively in one cultivar, could be considered potential markers of the individual cultivar. PCA allowed us to clearly discriminate the samples into three clusters: the first related to the Sanguinea peel, the second to the Faustrime peel, and a third group associated with the Pink Pearl peel along with the pulp of the three cultivars. Accordingly, the VOCs that mostly contributed to the differentiation of the three finger lime cultivars were also identified. Among them, D-limonene, sabinene γ-terpinene, α-pinene, α-phellandrene, β-myrcene, p-cymene, linalool, δ-elemene, ledene, bicyclogermacrene β-citronellol, α-bergamotene, α-caryophillene, and β-bisabolene, have been previously reported to exhibit important biological activities, suggesting that these cultivars, in addition to possessing unique volatile profiles, can show promise for several applications in pharmaceutical and food industry, namely for development of functional foods.

Volatile compounds, phenolic acid profiles and phytochemical content of five Australian finger lime (Citrus australasica) cultivars

Comparative analysis of three Australian finger lime (Citrus australasica) cultivars: Identification of unique citrus chemotypes and new volatile molecules

ABSTRACTFJAT-4748 is a bacterial strain isolated from forest soil samples taken from Dongba Valley, Lijiang, Kunming, Yunnan Province, PR China. This strain was identified as Lysinibacillus sp. based on a 16S rRNA gene sequence analysis. FJAT-4748 has been shown to possess antifungal activity against different fungi, including Colletotrichum acutatum, Aspergillus niger, Fusarium solani, Fusarium moniliforme and Fusarium oxysporum. The results of the present study indicate that this antifungal activity results from volatile organic compounds (VOCs) produced by this strain. The observed inhibition rates of VOCs from FJAT-4748 against these fungi were 100%, 100%, 37.20%, 18.94% and 7.64%, respectively. GC-MS analysis identified 24 VOCs from FJAT-4748, which included different categories of compounds, such as aldehydes, ketones, alcohols, aromatic hydrocarbons and alkanes. Of these 24 VOCs, the most abundant compound was 2-ethyl-1-hexanol, which constituted 36.24% of the total VOCs based on the relative peak area. In the in vitro C. acutatum mycelial growth assay, 2-ethyl-1-hexanol exhibited the strongest activity, with an inhibitory rate of 100% using 10 µL/plate of this VOC. The activity of benzaldehyde was lower. 2-decanone showed the weakest activity among the compounds tested. The inhibitory activity of an artificial mixture of three VOCs against the C. acutatum increased with the amount of artificial mixture used. The inhibition rate reached 100% using 30 µL/plate of this artificial mixture in the plate test. Taken together, these results show that the antifungal VOCs produced by Lysinibacillus sp. FJAT-4748 are potentially useful as agents for controlling anthracnose caused by Colletotrichum acutatum.

Airborne volatile organic compounds (VOCs) and semi-volatile organic compounds (SVOCs) are commonly quantitated by collecting the analytes on solid sorbent tubes or passive air samplers, followed by solvent extraction and instrumental analysis, or by grab bag/canister measurements. We report herein a user-friendly sampling method by breathing through polyurethane foam (PUF) face masks to collect airborne VOCs and SVOCs for chemical analysis. Specifically, dibasic esters, phthalate esters, polycyclic aromatic hydrocarbons, linalool, and nicotine trapped on PUF masks were quantitated by gas chromatography-mass spectrometry analysis as model VOCs and SVOCs. Results showed that the amount of these model VOCs and SVOCs trapped on PUF masks is proportional to the exposure duration. After cross-validation by parallel sampling using XAD-2 packed sorbent tubes, the method was used to quantitate VOCs and SVOCs in a variety of indoor and outdoor environments with varying air concentrations of analytes, temperature, humidity, and wind speed. Because air pollution is considered a major cause of many human diseases and premature deaths and the developed PUF mask sampling method showed high trapping efficiencies for both VOCs and SVOCs, it is believed that the developed sampling method will find wide application in assessing air pollution-associated disease risks with possible extension to more classes of VOCs and SVOCs when coupled with suitable instrumental detection methods.

As the establishment of environmental quality standards is being promoted, the reliability of environmental analysis is one of the most important issues. The environmental problems caused by toxic organic substances in particular have become serious in recent years; therefore, there is much demand for standard gases and solutions for these analyses. Because the exact concentrations of these calibration standards are of great significance to obtain reliable measurement values, the concentrations and uncertainties of these calibration standards are required. Volatile organic compounds (VOCs), such as trichloroethylene and benzene, are part of the emission and environmental quality standards; therefore, the calibration standards of these VOCs are demanded for environmental analysis. To ensure the reliability of these calibration standards, purity evaluations of these VOCs are essential. In many cases the purity of VOC is evaluated by the relative peak area percentage of the main component only by GC-FID analysis for convenience and versatility. However, because of the various kinds of organic compounds, including stabilizers, in the VOC, the sensitivities of the compounds against the main component will be different by GC-FID. Although the identification and measurement of these impurities will offer valuable information for calibration standards and for preparing multi-component standard gases and solutions, these impurities are rarely analyzed. For these reasons, purity evaluations and information on impurities in VOCs have great meaning for preparing standard gases and solutions. The purpose of this study is to establish a purity evaluation method for VOCs by GC-FID to prepare accurate standard gases and solutions. We selected seventeen frequently used VOCs, and attempted to determine each impurity and to estimate their uncertainties. In our work, the internal standard is added directly to the target VOC for a quantitative analysis, rather than using another solvent for dilution. The relative sensitivities of the impurities against the internal standard are measured in advance. As a result, we can analyze trace impurities in VOC precisely, and calculate the purity and uncertainty by the subtraction method. The VOC calibration standards for environmental analysis can be easily provided by the method proposed in this study.

<p indent=0mm>Ozone pollution is becoming increasingly serious in China, the accurate calculation of the volatile organic compounds (VOCs) contributions to ozone formation potential is the precondition for scientific and effective ozone control strategies. Maximum incremental reactivity (MIR) is an effective tool to evaluate VOCs’ reactivities, which may vary significantly because of different atmospheric conditions, VOCs compositions, and the relative abundances of VOCs and NO_{<italic>x</italic>}. Nevertheless, the most widely used MIR calculated by Carter based on 39 urban areas in the United States reflected the ozone formation potential of each VOCs species under atmospheric conditions in US. Whether their MIR values are appropriate under atmospheric conditions in China or not is still under discussion. In order to calculate the real contribution of VOCs to ozone formation, we firstly calculated the indigenized MIR values for Chinese megacities. Box model based on the second Regional Atmospheric Chemistry Mechanism (RACM2) was used to calculate the indigenized MIR for China. Observed data of four megacities (Beijing-Tianjin-Hebei, Yangtze River Delta, Pearl River Delta and Chengdu-Chongqing) which represent the typical atmospheric conditions in China were used as input parameters in calculation. We set two scenarios (Base scenarios and MIR scenarios) for MIR calculation, where Base scenarios were established by selecting the fourth highest ozone day during three years’ observed data, MIR scenarios were set by adjusting the NO_{<italic>x</italic>} availability to obtain the scenarios where ozone formation was most sensitive to VOCs. MIR values were calculated via the ratio of the change in ozone concentration due to the change in VOCs concentration divided by the change of VOCs concentrations in MIR scenarios. MIR_CHN (MIR values for four megacities) was obtained by averaging the normalized MIR values of all sites, with an uncertainty of 25%. Compared to the MIR calculated by Carter (MIR_USA in this study), our results showed a larger range values between the most active VOCs and the most inert VOCs. The MIR_CHN values of highly reactive VOCs (such as internal alkenes, butadiene, anthropogenic dienes, terminal alkenes, isoprene and o/m/p-xylene) were higher than MIR_USA values. Whereas MIR_CHN values of low reactive VOCs (HC5 and acetylene) were lower than MIR_USA values. Values of MIR_CHN and values of MIR_UAS were comparable for the moderate reactive VOCs. The differences between MIR_CHN and MIR_USA may be caused by differences in simulation time, reaction mechanism, and proportion of ozone precursors, NO_{<italic>x</italic>} availability, and VOCs compositions. Ozone formation potential of four megacities calculated by the MIR_CHN were much higher than that calculated by the MIR_USA, which meant that using MIR_USA may not only underestimate ozone formation potential, but also miss the key VOCs species in ozone formation in China. The key VOCs were isoprene, internal alkenes and m/p-xylene in ozone formation in China based on MIR_CHN calculation.

Many volatile organic compounds (VOCs) are used to produce various commercial products with aromas mimicking natural products. The VOCs responsible for aromas have been identified from many natural products. The current major strategy is to analyze chemical compositions and aroma qualities of individual VOCs using gas chromatography/mass spectrometry (GC/MS) and GC-olfactometry. However, such analyses cannot determine whether candidate VOCs contribute to the characteristic aroma in mixtures of many VOCs. In this study, we developed a GC/MS-based VOC collection/omission system that can modify the VOC compositions of samples easily and rapidly. The system is composed of GC/MS with a switching unit that can change gas flow routes between MS and a VOC collection device. We first applied this system to prepare gas samples for omission tests, and the aroma qualities of VOC mixtures with and without some VOCs were evaluated by panelists. If aroma qualities were different between the 2 samples, the omitted VOCs were likely key odorants. By collecting VOCs in a gas bag attached to the collection device and transferring some VOCs to MS, specific VOCs could be omitted easily from the VOC mixture. The system could prepare omission samples without chemical identification, preparation of each VOC, and laborious techniques for mixing VOCs, thus overcoming the limitations of previous methods of sample preparation. Finally, the system was used to prepare artificial aromas by replacing VOC compositions between different samples for screening of key odorants. In conclusion, the system developed here can improve aroma research by identifying key odorants from natural products.

Volatile organic compounds (VOCs) produced by indigenous Bacterium strain BS1727 as antifungal agents against Ganoderma boninense

Volatile organic compounds (VOCs) generated from naturally aged Japanese hanging scrolls and their model samples were measured using solid-phase microextraction-gas chromatography-mass spectrometry (SPME-GC-MS) to clarify the effect of different painting papers and raw materials on the degradation state of hanging scrolls. VOC-based degradation markers were identified and their applicability was considered for degradation evaluations of actual Japanese hanging scrolls. The relative peak areas of different VOC groups were calculated by normalising their peak areas to the total peak area of long-chain hydrocarbons. When a painting paper was immersed in a CuSO4・5H2O solution, or coated with an alum solution, the relative peak areas of furfural and carboxylic acids increased after accelerated ageing, while these relative peak areas decreased when animal glue was applied, indicating that animal glue inhibited the generation of VOCs. When the painting paper containing Cu2+ was stacked with lining paper, furfural and carboxylic acids migrated into the lining paper with ageing. Animal glue coated on the painting paper retarded this migration into the lining paper. For the lining paper coated with wheat starch paste, the relative peak areas of furfural, carboxylic acids, and aliphatic aldehydes did not change significantly with ageing, indicating that wheat starch paste did not contribute to paper degradation, although these relative peak areas increased when aged wheat starch paste was applied. These results indicate that the targeted VOCs are valid degradation markers of Japanese hanging scrolls.

A pilot-scale biocover was installed at a sanitary landfill for municipal waste, and the removal of volatile organic compounds (VOCs) by the biocover was evaluated for a long period of 550 days. The biocover (2.5 m W × 5 m L × 1 m H) was constructed with the mixture of soil, perlite, earthworm cast and compost (6:2:1:1, v/v). The total VOCs concentration of the inlet gas into the biocover was 820.3 ppb~7,217.9 ppb, and the total VOCs concentration of the outlet gas from the surface of the biocover was 12.6 ppb~1,270.1 ppb. The average removal efficiency of total VOCs was 87.6 ± 11.0% (60.5% for minimum and 98.5% for maximum). Toluene concentration was the highest among the inlet VOCs, followed by ethylbenzene, m, p-xylene and o-xylene. These aromatic VOCs accounted for more than 50% of the total VOCs concentration. Other than these aromatic VOCs, hexane, cyclohexane, heptane, benzene, and acetone were major VOCs among the inlet VOCs. Compared with the VOC profiles in the inlet gas, the relative contribution of dichloromethane to the outlet VOCs emitted from the biocover layer increased from 0.1% to 15.3%. The average removal efficiencies of BTEX in the biocover were over 84% during the operation period of 550 days. The average removal efficiencies of hexane, cyclohexane and heptane in the biocover were 86.0 ± 18.9%, 85.4 ± 20.4% and 97.1 ± 4.0%, respectively. The removal efficiency of VOCs in the biocover decreased not only when the ambient temperature had fallen below 5oC, but also when the ambient temperature had risen above 23oC. Information on the VOCs removal characteristics of the biocover installed in the landfill field can be useful for commercializing the biocover technology for the treatment of VOCs.

Composition and emission of VOC from biogas produced by illegally managed waste landfills in Giugliano (Campania, Italy) and potential impact on the local population

Identification of phenolic compounds from a unique citrus species, finger lime (Citrus australasica) and their inhibition of LPS-induced NO-releasing in BV-2 cell line