Chemical composition and antimicrobial activities of the essential oil from the seeds of Enterolobium contortisiliquum (leguminosae)

Seeds of Enterolobium contortisiliquum were subjected to steam distillation to obtain a light yellow essential oil in a yield of 3 ml/kg of seeds. The major components of the oil were identified using gas chromatography/mass spectrometry (GC-MS) and were furfural, limonene, linalool, estragole, carvone, and apiole with carvone representing more than 50% of the total composition. Antimicrobial activities of the essential oil were determined against four species of gram positive bacteria (Bacillus subtilis, Bacillus cereus, Staphylococcus aureus, Micrococcus luteus) and two gram negative bacteria (Klebsiella pneumoniae, Serratia Marcescencs). The essential oil inhibited the growth of all tested bacteria but was most effective against the gram positive bacteria. Chemicals that are responsible for the antibacterial effect of the essential oil were determined using the bio-autography thin layer chromatography (TLC) technique. The active compounds responsible for the activity were found to be carvone and estragole.     

Development of nanoemulsion from Vitex negundo L. essential oil and their efficacy of antioxidant,antimicrobial and larvicidal activities (Aedes aegypti L.)

Environmental Science and Pollution Research - It is believed that nanoemulsions were emerged as a promising candidate to improve the qualities of natural essential oil towards antimicrobial and...     

Chemical diversity and biological activities of essential oils from native populations of Clinopodium menthifolium subsp. ascendens (Jord.) Govaerts

Environmental Science and Pollution Research - This study is focused on the analysis of regional variation of the chemical compositions of three Clinopodium menthifolium subsp. ascendens (Jord.)...     

Chemical composition of precipitation at Marion Island (sub-Antarctic)

Over a 1-year period 16.40g Cl⁻m⁻², 10.35 g Na m⁻², 2.11 g SO₄-S m⁻², 1.24g Mg m⁻², 0.39 g K m⁻², 0.37 g Ca m⁻² and 0.21 g inorganic N m⁻² were deposited in precipitation 450 m inland on the eastern coastal plain of sub-Antarctic Marion Island (46°54′S, 37°45′E). Dissolved PO₄-P and organic forms of N were not detected in the precipitation samples. Concentrations of Cl⁻, Na, Mg, Ca and K, as well as the total ionic concentration in the precipitation samples were significantly negatively correlated with the amount of precipitation. The ionic concentration order (Cl > Na > SO₄-S > Mg > K ≈ Ca) in the precipitation was very similar to that in the surrounding ocean. It is likely that most of the inorganic N found in the precipitation originated in penguin rookeries on the nearby shore zone. A comparison is made between precipitation inputs of nutrients at the island and those at other subpolar sites in the S and N Hemispheres.     

Chemical composition of Swiss aerosols from the Jungfraujoch

Atmospheric aerosols have been sampled monthly during 19 months at the Jungfraujoch in Switzerland (3752 m above sea level). The geometric mean concentration of total suspended particulates is 3.1 μgm⁻³. Also the concentrations of 31 trace elements were determined in the samples. The concentration variations show a seasonal pattern for all elements, but most pronounced for the lithophilic elements. The geometric mean concentrations are compared to those measured at the other remote locations and at polluted sites. Rock and aerosol enrichment factors are calculated. The chemical compositions of the Jungfrau aerosol is very similar to that collected elsewhere. Also at remote locations the relatively volatile chalcophilic elements are enriched.     

Trypsin inhibitor,antioxidant and antimicrobial activities as well as chemical composition of potato sprouts originating from yellow- and colored-fleshed varieties

Abstract

Potato sprouts could be a valuable resource of phytochemicals such as secondary plant metabolites, potential antioxidants and nutritive compounds. In this work, potato sprout extracts of five varieties were examined; they differed in major glycoalkaloid content, trypsin inhibitor activity, total polyphenol content and antioxidant activity, as well as in antimicrobial activity against Gram?+?and G???bacteria, and yeast. Sprouts of colored-fleshed tubers were characterized by higher trypsin inhibitor activity than sprouts of yellow potatoes. The strongest microorganism growth inhibition effect was observed for macerate with sprouts from the purple-fleshed Blaue Annelise variety against B. subtilis, whereas C. albicans yeasts were sensitive to macerates with sprouts from purple-fleshed Blue Congo and yellow-fleshed Vineta potato varieties.     

Chemical composition of freshsnow samples from the southern slope of Mt. Everest region (Khumbu-Himal region,Nepal)

In 1998 fresh surface snow samples were collected, no more than 2 days after the snowfall, along the Khumbu valley, and its lateral valleys (Kongmala and Changri Nup), at the end of the summer monsoon period. Samples from the Island Peak and Pumori slopes were also collected by climbers during pre- and post-monsoon season at altitudes ranging from 5300 to 6100 m a.s.l. Conductivity, pH and major inorganic ions were measured in samples and relative field blanks. Chemical results were subjected to principal component analysis (PCA) in order to distinguish different sources of ions and study spatial and temporal distribution of ion concentrations. Two main factors, accounting for more than 80% of the total variance, were found. The two factors were correlated to two different sources, one representing local transport and background contribution, and the other related to monsoon circulation. Concentrations of the main ions were compared to those measured in other remote areas, with particular regard to elevated areas in Central Asia.     

Chemical composition of fogwater in an urban area: Strasbourg (France)

To investigate the acidity and to identify the predominant compounds, this work presents the chemical analysis of 18 fogwater samples collected during the year 1991 in Strasbourg, in the east of France. For each fog event, two droplet size categories (2-6 microm and 5-8 microm) have been separately collected and 16 ionic components have been analysed. These two fraction sizes were chosen because they correspond approximately to the size range that can penetrate the human lung and they may have possible health effects. The dominant species were NH4+, NO3-, SO4(2-) and Cl-, with a maximum level of 12,640, 17,270, 21,620 and 13,540 microeq litre(-1), respectively. For most of the fog events the highest concentrations of all analysed species were observed in the 2-6 microm droplets. pH values ranged between 2.79 and 5.70 and the fogwater acidity was governed by three strong acids, H2SO4, HNO3 and HCl and was partially neutralised by NH3 and probably by the presence of CaCO3 in the 'loess', which is the major constituent of soils in the upper Rhine valley. In other respects the acetate/formate ratio (methanoate/ethanoate), generally lower than 1, indicates an important pollution due to automobile exhaust, although the Pb concentrations are moderate due to the general use of unleaded gasoline in France since 1989.     

The essential oil qualitative and quantitative composition in the needles of Pinus sylvestris L. growing along industrial transects

The aim of this study was to evaluate composition of the essential oils in the needles of Pinus sylvestris growing in the areas affected by a cement factory (CF), and an oil refinery (OR). Volatile components of the needles were analyzed by GC and GC/MS. The most heavily polluted CF stand had significantly higher concentration of gamma-Terpinene, Caryophyllene oxide in the current-year needles, while higher concentration of delta-3-Carene, alpha-Terpinene, gamma-Terpinene and Terpinolene was documented for 1-year-old needles. The most heavily polluted OR stand had a significantly higher concentration of Sabinene+beta-Pinene, 1-epi-Cubenol in the current-year needles and a significantly higher concentration of Camphene, Sabinene+beta-Pinene, Myrcene, alpha-Cadinene, 1-epi-Cubenol in the 1-year-old needles than the least polluted site. Along transects an increase in the amount of some diterpenes and a decrease in the components of the shorter chain essential oils was observed. These effects could be at least partially attributed to SO(2).     

Chemical composition of water from roofs in Gdansk, Poland

This study deals with the assessment of roof runoff waters from the region of Gdansk collected during the winter season (2007/2008). The chemical analysis includes 16 chemical variables: major ions, PAHs and PCBs measured at 3 sampling sites for 6-14 rain events. Although the data set is of limited volume the statistical data treatment using self-organizing maps (SOM) reveals the main factors controlling roof runoff water quality even for a data set with small dimension. This effort for explanation of the identified factors by the possible emission sources of the urban environment and air-particulate formation seems to be very reliable. Additionally to the roof runoff water quality factors the rain events patterns are found: “background” group of events and groups formally named “PAHs”, “PCBs” and “air-borne particles” - dominated events. The SOM classification results give an opportunity to uncover the role of roof “impact” on the runoff waters.Rain runoff water quality is described by four latent factors and the “roof” impact is uncovered.     

Chemical composition of fresh snow from Gulmarg, North India

The chemical composition and pH of 30 fresh snow samples collected during December 1986 to May 1987 at Gulmarg (34 degrees 03' N, 74 degrees 24' E, 2655 m above mean sea level), a remote place in north India, were studied. The snow samples were, by and large, alkaline in nature and were largely influenced by non-marine aerosols. The concentrations of cations (Ca(2+), K(+) and Mg(2+)) were more than the anions (SO(2-)(4) and NO(-)(3)). Factor analysis indicated that most of the ionic components were transported into the region during the period of measurements. The transport of ionic components could be attributed to the passage of western disturbances over this region. The comparison of concentrations of anions and cations in the snow samples at Gulmarg with those reported from a few countries in the west revealed that the composition of Gulmarg snow largely differs in the concentrations of cations rather than anions. Among the cations, the concentration of Ca(2+) was high at Gulmarg and this could be responsible for buffering the pH of snow in the alkaline range.     

Chemical fingerprinting applied to the evaluation of marine oil pollution in the coasts of Canary Islands (Spain)

Chemical fingerprinting approach to environmental assessment is illustrated in the evaluation of marine oil pollution in the coasts using two limpet species as bioindicator organisms, and based on profiles and concentrations of n-alkanes and aromatic hydrocarbons in their tissues. Accidental and chronic releases of hydrocarbons can contaminate the marine environment of the Canary Islands not only because of their geographical situation but also because of the very dense tanker traffic around. This situation affects coastal areas, fishing activities, tourism resort, etc. Concentrations of n-alkanes and aromatic hydrocarbons (polycyclic aromatic hydrocarbons and methyl-polycyclic aromatic hydrocarbons) in the soft tissues of the marine intertidal and subtidal limpets, Patella crenata and Patella ullysiponensis aspera, were evaluated. Limpet samples were collected at monthly intervals, at three locations on the southeast coast of Tenerife over a 3-year period (1991-93). Levels of hydrocarbons found in limpets are similar to concentrations found in unpolluted areas around the world. From application of principal component analysis, the interpretation of variable loading plots gives information on variable correlation and can be used to distinguish among potential sources of pollution and the ability of studied molluscs to be used as bioindicator organisms.     

老港填埋场渗滤液性质随工艺变化研究

经老港填埋场渗滤液处理系统的各处理单元处理后的流出液,用不同孔径的系列膜进行了梯度分离。分离前后的渗滤液进行了TOC、TP、TN、氨氮和可溶性P等参数的测定,并建立了各参数与不同孔径膜的关系。结果表明,此工艺对老港填埋场渗滤液的处理具有一定的功效;随着处理工艺的进行,渗滤液的组成发生了较大的改变,其中细胶体部分的百分含量增加,而可溶性部分降低;渗滤液的绝大部分污染物质集中于可溶性部分,而渗滤液中的P主要与大分子的悬浮物和粗胶体结合。     

Chemical composition of rainwater in the northeastern Romania, Iasi region (2003–2006)

Chemical composition of rainwater was studied in the northeastern Romania, Iasi region, and the concentrations of major inorganic and organic ions were measured in samples collected between April 2003 and December 2006. The pH of the rainwater is 5.92 (volume weighted mean average, VWM) suggesting a sufficient load of alkaline components neutralizing its acidity. On average, 97% of the acidity in the collected samples is neutralized by CaCO₃ and NH₃. Clear seasonal variations were observed for some of the identified ions (e.g., SO₄²⁻, NO₃⁻, Ca²⁺, NH₄⁺). The data obtained during this work revealed that both concentrations and fluxes of anthropogenic source-related ions (e.g., SO₄²⁻, NO₃⁻ and NH₄⁺) are among the highest reported for European sites. It is shown that meteorology and long-range transport processes may concur to their high levels.     

Pesticide and plasticizer residues in bergamot essential oils from Calabria (Italy)

Organophosphorus and organochlorine pesticides, phosphorated plasticizers, chloroparaffins and phthalate esters contamination in bergamot essential oils produced in Calabria in the crop years 1999-2000 was studied by HRGC in connection with detectors FPD, ECD, MS. Residues of dicofol and tetradifon were found in oils from both crop years. The mean dicofol concentration was 0.26 mg/l in samples from 1999 and 0.20 mg/l in those from 2000; the mean tetradifon content was 0.06 mg/l for both the crop years. Among plasticizers, residues of diisobutyl phthalate, di-n-butyl phthalate, and bis(2-ethylhexyl) phthalate were found in samples from crop years 1999 and 2000, the mean content were 1.22 and 1.23 mg/l, 1.51 and 1.65 mg/l, 1.38 and 1.42 mg/l respectively.     

Chemical composition of selected seaweeds from the Indian Ocean,KwaZulu-Natal coast,South Africa

The chemical composition of three edible seaweeds (Codium capitatum, Hypnea spicifera and Sargassum elegans) and two inedible seaweeds (Halimeda cuneata and Spyridia hypnoides) from the Indian Ocean along the KwaZulu-Natal East Coast, South Africa were investigated as a function of seasonal variation. The proximate compositions of the edible seaweeds were determined. In edible seaweeds, the moisture level ranged from 85.4 to 89.5%, protein from 6.1 to 11.8%, lipids from 7.5 to 13.1% and carbohydrates from 37.8 to 71.9%. Elemental concentrations in the five studied seaweeds varied significantly with season (P < 0.05) with mean elemental concentrations (in µg g^?1, dry weight) being: Ca (29 260), Mg (6 279), Fe (1 086), Cu (145.9), Mn (48.32), As (24.29), Zn (15.65), Ni (9.83), Cr (5.78), Pb (4.84), Co (0.87) and Se (0.86). The concentrations of As were particularly high in S. elegans, ranging from 94.70 ± 6.6 µg g^?1 in winter to 65.10 ± 2.3 µg g^?1 in summer. Hierarchical cluster analysis showed similar distribution of elements in edible seaweeds which was dissimilar to that in inedible seaweeds. This study suggests that edible macro alga, C. capitatum and H. spicifera, could be potential sources of most essential nutrients and may contribute positively to the diet without posing the risk of adverse health effects due to low concentrations of toxic elements. However, due to high levels of As in S. elegans, its consumption should be moderated to reduce dietary exposure to this toxic element.     

Production of granular activated carbon from food-processing wastes (walnut shells and jujube seeds) and its adsorptive properties

Commercial activated carbon is a highly effective absorbent that can be used to remove micropollutants from water. As a result, the demand for activated carbon is increasing. In this study, we investigated the optimum manufacturing conditions for producing activated carbon from ligneous wastes generated from food processing. Jujube seeds and walnut shells were selected as raw materials. Carbonization and steam activation were performed in a fixed-bed laboratory electric furnace. To obtain the highest iodine number, the optimum conditions for producing activated carbon from jujube seeds and walnut shells were 2 hr and 1.5 hr (carbonization at 700°C) followed by 1 hr and 0.5 hr (activation at 1000°C), respectively. The surface area and iodine number of activated carbon made from jujube seeds and walnut shells were 1,477 and 1,184 m²/g and 1,450 and 1,200 mg/g, respectively. A pore-distribution analysis revealed that most pores had a pore diameter within or around 30–40 Å, and adsorption capacity for surfactants was about 2 times larger than the commercial activated carbon, indicating that waste-based activated carbon can be used as alternative.

Implications:Wastes discharged from agricultural and food industries results in a serious environmental problem. A method is proposed to convert food-processing wastes such as jujube seeds and walnut shells into high-grade granular activated carbon. Especially, the performance of jujube seeds as activated carbon is worthy of close attention. There is little research about the application of jujube seeds. Also, when compared to two commercial carbons (Samchully and Calgon samples), the results show that it is possible to produce high-quality carbon, particularly from jujube seed, using a one-stage, 1,000°C, steam pyrolysis. The preparation of activated carbon from food-processing wastes could increase economic return and reduce pollution.     

Chemical composition of fine particles from incense burning in a large environmental chamber

 This study is aimed to characterize the major chemical compositions of PM_2.5 from incense burning in a large environmental chamber. Chemical analyses, including X-ray fluorescence for elemental species, ion chromatography for water soluble inorganic species (chloride, nitrate, sulfate, sodium, potassium, ammonium) and thermal/optical reflectance analysis for carbon species were carried out for combustion of three incense categories (traditional, aromatic and church incense). The average concentrations from incense burning ranged from 139.8 to 4414.7 μg m⁻³ for organic carbon (OC), and from 22.8 to 74.0 μg m⁻³ for elemental carbon (EC), respectively. The average OC and EC concentrations in PM_2.5 of three incense categories were in the order of church incense>traditional incense>aromatic incense. OC/EC ratios ranged from 7.0 to 39.1 for the traditional incense, with an average of 21.7; from 3.2 to 11.9 for the aromatic incense, with an average of 7.7. The concentrations of Cl⁻, SO₄²⁻, Na⁺ and K⁺ were highly variable. On average, the inorganic ion concentration sequence was traditional incense>church incense>aromatic incense. The profiles for elements were dominated by Na, Cl and K. In general, the major components in PM_2.5 fraction from incense burning are OC (especially OC2, OC3 and OC4), EC and K.     

Chemical and biochemical generation of carbohydrates from lignocellulose-feedstock (Lupinus nootkatensis)--quantification of glucose

Different chemical and enzymatic methods were applied for the hydrolysis of main stems from Lupinus nootkatensis (harvest November 2002). The whole process (all steps) is based on the lignocellulose-feedstock biorefinery regime. The acid hydrolysis of L. was performed with concentrated hydrochloric acid; advantages in this process are exothermic hydrolysis and the possibility of acid recovery. Enzymatic hydrolysis achieved high yields of fermentable carbohydrates (regarding to input cellulose) with high selectivity. However, this way requires the generation of cellulose from L. by chemical pulping. Monosaccharide derivatives thus obtained were identified by their GC retention times and the corresponding MS fragmentation. Hexamethyldisilazane was used as derivatization reagent to prepare the trimethylsilyl derivatives of the carbohydrates and of the degradations products of cellulose from the different fractions. The glucose content was quantified by GC peak integration with respect to an internal standard.