INAA of essential micronutrients in <Emphasis Type="Italic">Terminalia arjuna</Emphasis> bark powder: a versatile heart tonic

Five bark powder samples of Arjuna (Terminalia arjuna) having different origins including two commercial brands were analyzed for 8 minor (Al, Na, K, Mg, Ca, P, Cl, Fe) and 19 trace (As, Ba, Br, Co, Cr, Cs, Cu, Eu, Hg, La, Mn, Rb, Sb, Sc, Sm, Sr, Th, V, Zn) elements by INAA. Also concentrations of Ni, Cd and Pb were determined by AAS and of Sn by ICP-MS. Arjuna bark powder is enriched in Ca (34.1 ± 10.6 mg/g), Mg (5.41 ± 1.93 mg/g), K (5.87 ± 2.18 mg/g), Cl (4.0 ± 2.2 mg/g) and Fe (2.99 ± 1.77 mg/g) with significant amounts of Cr (6.9 ± 4.0 μg/g), Mn (75.5 ± 24.8 μg/g), Sr (114 ± 69 μg/g) and Zn (11.9 ± 8.9 μg/g). Several toxic elements such as As (78.6 ± 19.9 ng/g), Cd (5.60 ± 9.04 μg/g), Hg (69 ± 41 ng/g) and Pb (5.0 ± 3.5 μg/g) were also detected.     

Determination of trace elements in olive oil by ICP-AES and ETA-AAS: A pilot study on the geographical characterization

The determination of trace elements in edible oils is important because of both the metabolic role of metals and possibilities for adulteration detection and oil characterization.The most commonly used techniques for the determination of metals in oil samples are inductively coupled plasma atomic emission spectrometry (ICP-AES) and atomic absorption spectrometry (AAS). For this study, a microwave assisted decomposition of the olive oil in closed vessels using a mixture of nitric acid and hydrogen peroxide was applied as sample preparation.The low achievable LODs enable the determination by ICP-AES of even very low concentrations of most elements of interest. The proposed ICP-AES method permits the determination of Ca, Fe, Mg, Na, and Zn in olive oils. Elements present in small amounts (Al, Co, Cu, K, Mn, Ni) were measured by ETA-AAS in the same sample digest. The concentrations of Al, Co, Cu, K, Mn, and Ni were in the range from 0.15 to 1.5 μg/g and differ according to the geographical origin of the oils. For the amounts of Fe, Mg, Na, and Zn in the samples, no significant differences according to the geographical origin of the oils could be observed, the mean concentrations being 15.31, 3.26, 33.10, and 3.39 μg/g, respectively. The Ca content varies in the range of 1.3 to 9.0 μg/g.The dependency of the trace elemental content of olive oils on their geographical origin can be used for their local characterization.     

GC–MS characterisation and biological activity of essential oils from different vegetative organs of Plectranthus barbatus and Plectranthus caninus cultivated in north Italy

Essential oils (EOs) from the roots, stems and leaves of Plectranthus barbatus (A) and Plectranthuscaninus (B), cultivated in north Italy, were obtained by steam distillation and chemically characterised by gas chromatography–mass spectrometry. The highest yields were obtained from roots (268.15 and 673.60 mg/kg from A and B), followed by leaves (64.34 and 26.65 mg/kg) and stems (19.76 and 18.63 mg/kg). A total of 128 structures were identified in A and 121 in B. Fe⁺⁺ chelating and antiradical activities (DPPH and ABTS) were evaluated: root and stem EOs showed the strongest activities, while EOs from leaves did not show relevant activities. All EOs were tested for their in vitro antimicrobial activity, showing optimal growth-inhibition in antibiogram (?>35 mm) and MIC tests (32–64 μg/mL) against Candida albicans, while EOs from leaves of both species showed a good activity (25 < ? < 34 mm, MIC 64–128 μg/mL) against Escherichia coli.     

Toxic and essential element concentrations in different honey types

The physicochemical parameters (free acidity, moisture content, sucrose content, hydroxymethylfurfural, reducing sugars, electrical conductivity, diastase activity and water-insoluble content), elements (Cu, Fe, Zn, Mn, Cr, Co, Ni, Se, K, Na, Ca, Mg) and heavy metal/metalloid concentrations (Cd, Hg, Pb and As) of 84 honeys (linden, multifloral, honeydew and acacia) from Serbia, were analyzed using ICP-MS. Concerning the physicochemical parameters, all tested honeys were found to meet European Legislation (EC Directive 2001/110). Potassium was the major element, ranging between 943.9 ± 538.6 mg/kg and 2563 ± 1817 mg/kg. Statistical analysis showed significant differences in the concentrations of Zn, Mn, Co and Na between the honeys. Selenium and Hg levels were below the limits of detection. Positive correlations were found between electrical conductivity and most of the elements. The present study showed that Serbian honey examined were of good quality according to its physicochemical parameters and met safety criteria concerning the concentrations of Cd, Hg, Pb and As.     

Antibacterial activity of commercially available plant-derived essential oils against oral pathogenic bacteria

This work investigated the antibacterial activity of 15 commercially available plant-derived essential oils (EOs) against a panel of oral pathogens. The broth microdilution method afforded the minimum inhibitory concentrations (MICs) and minimum bactericidal concentrations (MBCs) of the assayed EOs. The EO obtained from Cinnamomum zeylanicum (Lauraceae) (CZ-EO) displayed moderate activity against Fusobacterium nucleatum (MIC and MBC = 125 μg/mL), Actinomyces naeslundii (MIC and MBC = 125 μg/mL), Prevotella nigrescens (MIC and MBC = 125 μg/mL) and Streptococcus mutans (MIC = 200 μg/mL; MBC = 400 μg/mL). (Z)-isosafrole (85.3%) was the main chemical component of this oil. We did not detect cinnamaldehyde, previously described as the major constituent of CZ-EO, in specimens collected in other countries.     

Assessment of metal contamination in an urban drainage system (using water and tilapia, Oreochromis spp.) in view of human health effect. A case study of some selected communities in Cape Coast township in Ghana

This research work aimed at studying the metal content of water and tilapia fish sample, Oreochromis spp., from a wastewater-fed pond around the University of Cape Coast community using instrumental neutron activation analysis. The metals studied were Al, As, Ca, Co, Cr, Cu, Fe, K, Mg, Mn, Na, V and Zn. In the water samples the order of elemental concentrations at sampling point 1, in ??g/g, was K (75.96?±?0.92), Na (18.52?±?0.35), Al (6.00?±?0.89), Mn (3.28?±?0.44), As (3.08?±?0.40), Mg (1.56?±?0.17), Ca (0.70?±?0.08), Cu (0.54?±?0.08) and V (0.04?±?0.01). Co, Cr, Fe and Zn were below detection limits of INAA. The order of elemental concentrations in the water at point 2 was as follows: Na (4.99?±?0.14), K (4.82?±?0.89), Mn (4.40?±?0.53), Mg (2.92?±?0.37), Al (1.98?±?0.21), As (0.69?±?0.10), Ca (0.24?±?0.07) and V (0.23?±?0.06) with Co, Cr, Cu, Fe and Zn falling below the detection limit of INAA. The concentrations recorded for Al, As, Cu and Mn in the water samples were all above WHO permissible limits. The mean levels of heavy metals in the soft tissue of tilapia was of the order: K?>?Mg?>?Fe?>?Ca?>?Na?>?Al?>?Mn?>?Zn?>?V?>?Cu?>?Cr?>?Co. Arsenic was below detection limit. The transfer factor values calculated for the metals Al, Ca, K, Mg, Mn, Na and V were all greater than one indicating movement of metals from the water column to the tilapia species. The hazard index (HI) calculated for Al, Fe, Mn and V suggested possible occurrence of adverse health effects (HI?>?1) where as the HI value obtained for Cr, Cu and Zn (i.e., HI?<?1) suggested unlikely adverse effects occurring.     

Multielement analysis of green coffee and its possible use for the determination of origin

Using instrumental neutron activation analysis (INAA), graphite furnace atomic absorption spectrometry (GFAAS), flame atomic absorption spectrometry (FAAS) and combustion elemental analysis, green coffees of the Arabica species produced in crop year 1987/88 in Colombia, Costa Rica, Cuba, El Salvador, Mexico, Nicaragua, Panamá and Papua New Guinea were analysed for the elements Ba, Br, C, Ca, Co, Cr, Cu, Cs, Fe, H, K, La, Mg, Mn, N, Na, Rb, Sc, Sr and Zn. In accordance with the concentrations determined, the elements could be ranked into five groups: Sc (sub-ppb level); Br, Co, Cr, Cs and La (ppb level); Ba, Cu, Fe, Mn, Na, Rb, Sr and Zn (ppm level); Ca and Mg (%o level); and C, H, K and N (% level). On the basis of the results obtained, an attempt was made to establish the origin of the green coffee via its elemental composition. Among the investigated elements, manganese was found to be best suited as an indicator for this purpose. However, the elements C, Co, Cs, Na and Rb proved to be of interest too.     

Effect of grinding method on the analysis of essential oil from <Emphasis Type="Italic">Baccharis articulata</Emphasis> (Lam.) Pers.

Grinding methods were evaluated aiming to determine yield and composition of essential oils (EOs) from Baccharis articulata (Lam) Pers., called as carqueja, a native plant from South Brazil. Cryogenic, knife (with and without cooling) and ball mills were used. The major constituents found in EOs were β-pinene, caryophyllene, spathulenol and caryophyllene oxide, but differences in 21 compounds were observed. All grinding processes reduced monoterpenes and oxygenated sesquiterpenes with concentration of hydrocarbon sesquiterpenes. The sesquiterpenes (hydrocarbons and oxygenated) were found from 63.55 to 86.02% while the monoterpene hydrocarbons’ concentration ranged from 13.98 to 36.45%. Plants milled with knife mill provided EOs with profile similar to those not grinded. Despite the lower working temperature, cryogenic milling resulted in smaller EO yield (0.40 ± 0.03%) in comparison to other grinding methods (yields from 0.50 ± 0.02 to 0.56 ± 0.03%) and different chromatographic profile. Microscopic analysis showed the smaller particle size provided by cryogenic grinding, which leads to glandular trichome rupture and consequently to loss of EOs. This study showed that grinding should be carefully evaluated to provide reproducible results in essential oil analysis.     

Concentrations of major and trace elements in polished rice and paddy soils collected in Aomori,Japan

Rice grain samples and surface paddy soil samples were collected from 20 sites throughout Aomori Prefecture, Japan, and the concentrations of 25 elements in the polished rice and 33 elements in the soils were determined by neutron activation analysis, inductively coupled plasma-mass spectrometer or atomic adsorption spectrometer. The range of essential element concentrations in the polished rice was within one order of magnitude, however, the range for most of the trace elements was more than one order of magnitude. The range of element concentrations, except for I, in the paddy soils was within one order of magnitude. The ±95% confidence intervals of the soil-to-polished rice transfer factors for all elements, except for Pb, were within two orders of magnitude, and the geometric mean values were as follows: Cl, Mo and Zn (0.1–1); K, Cu, Cd, Rb, Mg, Mn, and Ag (0.01–0.1); Ni, As, Ca, Se and I (0.001–0.01); Na, Cs, Sr, Co, Cr, V, Ba, Pb, Fe and Al (<0.001).     

Elemental fingerprinting of gypsum drywall using sector field ICP-MS and multivariate statistics

Outgassing of volatile sulphur compounds from gypsum drywall from some sources has resulted in odours, corrosion of wiring and metals and health problems for homeowners. Infrared spectroscopy has been the primary analytical tool to identify ‘problematic’ drywall. In this paper, we demonstrate that elemental fingerprinting using inductively coupled plasma mass spectrometry and multivariate statistics is an effective alternative. The approach also showed potential in determining the geographic source of gypsum. Nineteen elements (Al, Ba, Ca, Cd, Co, Cr, Cs, Cu, Fe, Mg, Mn, Ni, Pb, Rb, Sr, Tl, U, V and Zn) were measured in 20 samples of drywall, half of which were classified as positive for contamination by Fourier Transform Infrared Spectroscopy. Gypsum from three different mines and a flue gas desulphurisation plant were also analysed. Principal component analysis and multivariate analysis of variance of the elemental data showed significant differences between the problematic and non-problematic drywall and between sources of gypsum. Strontium averaged 1800 ± 500 µg/g in problematic drywall compared to 400 ± 100 µg/g in non-problematic drywall (p < 0.0001).     

Determination of elemental and nutrient composition of water,clam mantle and shell of the Volta clam (<Emphasis Type="Italic">Galatea paradoxa</Emphasis>) using neutron activation analysis

The Volta clam Galatea paradoxa is a highly priced shellfish providing nutrition, jobs and poverty alleviation for the inhabitants of the lower Volta estuary. Clams are filter feeders straining particulate materials in the surrounding water, thus concentrating microorganisms and other metal elements in the gut and mantle which present possible health hazards. The elemental composition of the water, clam mantle, gut, shell, and bottom sediments were determined using Neutron Activation Analysis for the presence of Ca, Cl, Cu, Mg, Mn, V, Fe, Co, Br, Na and K. Proximate analysis of the mantle for the levels of protein, fat, carbohydrate, ash, wood fiber, phosphorus, free fatty acids and energy were carried out using the method of the Association of Official Analytical Chemists. The riverine water was laden with heavy metals V, Co, Cu, Mn, and Fe, as well as Al. These same metallic elements were detected in higher concentrations in the bottom sediments. Bioaccumulation factor (BAF) which is the measure of the distribution of heavy metals between water and biota (Clam mantle and gut), ranged from 2 to 145 times, depending on the type of contaminant. The clam meat contained high protein (15.3 ± 0.2%), no crude fiber, low fat content (1.80 ± 0.11%), fatty acids as oleic (25.2 ± 0.1%), energy (85.5 ± 0.21 kcal/100 g), carbohydrates (22.10 ± 0.03%), P (485 ± 1 mg/100 g), Ca (793 ± 75 mg/kg), Mg (860.3 ± 90.0 mg/kg). The high concentration of Ca (21,402.7 ± 797.0 mg/kg), Fe (18,071.2 ± 94.0 mg/kg), K (96 ± 14 mg/kg), Mg (540.8 ± 81.1 mg/kg), Na (4,570.0 ± 0.2 mg/kg) gives credence to the use of the shell for poultry feed mineral supplements, and in the emulsion paint manufacturing industry.     

Application of INAA in the assessment of selected elements in cancellous bone of human iliac crest

The effect of age and sex was investigated on the concentration of chemical elements in intact cancellous bone of iliac crest of 74 relatively healthy, 15–55 years old women (n = 29) and men (n = 45). Concentrations of Ca, Cl, K, Mg, Mn, Na, P, and Sr in bone samples were determined by instrumental neutron activation analysis using short-lived radionuclides. Mean values (M±S.E.M.) of the mass fraction of the investigated elements (on dry weight basis) for female and male all together were: 127±4 g/kg, 1620±80 mg/kg, 1310±70 mg/kg, 1550±50 mg/kg, <0.32±0.02 mg/kg, 4240±110 mg/kg, 61.8±1.8 g/kg, and 235±18 mg/kg, respectively. The statistically significant (≤0.05) decrease of Ca, Mg, and P concentrations in the iliac cancellous bone with age was found only for women. Sex-related comparison has shown that the mean values of Mg mass fractions in male bone samples were less than in female ones.     

Appraisal of venomous metals in selected crops and vegetables from industrial areas of the Punjab Province

Due to the inadequate water sources, usually sewerage water and industrial effluents are being use for irrigation of the agricultural land around the industrial areas in Pakistan wherein crops and vegetables are cultivated. As untreated effluents contain heavy elements, toxic metals and organic pollutants that may find its way through food chain to general public and may cause health hazards. It is, therefore, mandatory to assess the toxic metals in such crops and vegetables. In this regard, samples of corn, millet, cabbage, spinach and potato were collected within the vicinity of industrial areas of the Faisalabad and Gujranwala regions. The food samples were analyzed using neutron activation analysis (NAA) technique. The highest concentration values of Arsenic (1.9 ± 0.1 μg/g) and Cobalt (0.85 ± 0.01 μg/g) were found in cabbage whereas Manganese (91.6 ± 0.2 μg/g), Antimony (0.15 ± 0.03 μg/g) and Selenium (1.1 ± 0.1 μg/g) were observed in spinach and Chromium (9.63 ± 1.3 μg/g) was found in millet crop. The observed concentrations of all the toxic and heavy metals in crops and vegetables are higher than those reported in the literature.     

玫瑰花茶的金属元素含量及其保健功能分析

采用V（HNO3）＋V（HClO4）=5＋1对玫瑰花茶进行消解,用火焰原子吸收光谱法测定了其中金属营养元素的含量。结果表明,玫瑰花茶中含有丰富的人体所必需的金属元素,其中钾、钙、钠、镁、铁、锰、铜、锌含量分别为11．6559,6．5642mg／g,23．3147μg/g,2．0533mg／g,25．8711,20．5897,7．9107,23．2493μg/g,各元素比例有利于人体吸收,具有较高的营养保健价值,为人们选用花茶提供了一定的理论依据。     

Chemical composition and in vitro anticancer,antimicrobial and antioxidant activities of essential oil and methanol extract from Rumex nervosus

Chemical composition, antioxidant, anticancer, and antimacrobial activities of essential oil obtained from leaves of Rumex nervosus has been evaluated here for the first time. GC/MS analysis reveals the presence of Palmitoleic Acid (28.35%) and Palmitic acid, (25. 37%) as their methyl ester as major components. The essential oil showed significant DPPH radical scavenging activity (94.907 ± 0.1089% and 94.003 ± 0.0749%) at concentration (100 and 80) μg/mL respectively. The oil showed promising activity against staph aureus, while showed weak activity against (Hela and 3T3) cell lines. The crude extract / fractions of R. nervosus (leaves) showed significant antioxidant activity at dose (100 and 80) μg/mL. Futhermore the crude showed significant activity against (MCF-7 and MDA-MB-231) cell lines with IC₅₀ (20.5138 ± 0.933 and 25.1728 ± 0.9176) μg/mL respectively, and chloroform fraction showed good activity against (MCF-7 and MDA-MB-231) cell lines with IC₅₀ (31.154 ± 0.965 and 42.269 ± 2.1045) μg/mL.     

Development and validation of a multiresidue method for the simultaneous determination of organophosphorus insecticides and their toxic metabolites in sugarcane juice and refined sugar by gas chromatography with flame photometric detection

A multiresidue method has been developed and validated for the simultaneous determination of organophosphorus insecticides and their toxic metabolites in sugarcane juice and refined sugar by gas chromatography with flame photometric detection. Limits of quantification of the method varied between 0.007 and 0.01 μg/g. Ethyl acetate based extraction followed by dispersive solid‐phase extraction cleanup with primary secondary amine yielded internationally acceptable recoveries of acephate, chlorpyrifos, dichlorvos, monocrotophos, malathion, malaoxon, phorate, phorate‐sulfoxide, phorate‐oxon, phorate‐sulfone, and quinalphos from selected matrices. The recoveries of target analytes from cane juice were 75.55 ± 0.5–102.57 ± 4.2, 77.45 ± 4.7–103.33 ± 3.3, and 80.55 ± 6.6–105.82 ± 9.8% at 0.01, 0.02, and 0.1 μg/g levels of fortification, respectively. The recoveries from cane sugar were 73.24 ± 3.5–104.47 ± 1.9, 75.23 ± 1.5–116.10 ± 3.7, and 70.75 ± 5.7–110.15 ± 2.7%, respectively at 0.01, 0.02, and 0.1 μg/g levels of fortification. Matrix effect and measurement uncertainty were within the permissible limit (less than 20%) as prescribed for pesticide residue analysis.     

Geochemistry and health burden of radionuclides and trace metals in shale samples from the North-Western Niger Delta

Organic sedimentary rock samples were collected from three Oil Wells in the North-Western Niger Delta, Nigeria in order to determine their natural radioactivity and elemental geochemistry, with the aim of determining the concentrations of major radionuclides and their radiological and environmental health implication. The PIXE method of IBA technique and an accurately calibrated Si(Li) detector system was used to measure the elemental concentration of the sediment samples. The radionuclides identified belong to the decay series of naturally occurring radionuclides headed by ²³⁸U and ²³²Th along with the non-decay series radionuclide, ⁴⁰K. The activity concentrations of the radionuclides and their derived dose were then calculated. The average activity concentrations of ⁴⁰K were 248 Bq/kg for Well A, 261 Bq/kg for Well B and 273 Bq/kg for Well C. For ²³²Th the activity concentrations were 1,043 Bq/kg for Well A, 1,400 Bq/kg for Well B, 1,434 Bq/kg for Well C. ²³⁸U activity concentrations were 2,210, 3,508 and 250 Bq/kg for the Oil Wells A, B, C, respectively. The equivalent dose ranges from 8.5 ± 1.1 to 24.3 ± 2.1 mSv/year with a mean of 14.5 ± 2.2 mSv/year for Oil Well A, 2.4 ± 0.1–75.0 ± 1.2 mSv/year with a mean of 21.5 ± 1.1 mSv/year for Oil Well B and 3.7 ± 0.2–10.7 ± 0.6 mSv/year with a mean of 9.4 ± 2.5 for Oil Well C. The detected trace metals were majorly V, Ni, Pb, Fe, Cr, Cu, Zn, Co and their concentrations together with those of the radionuclides are compared with the relevant world standard limits. The results obtained were high, and hence, the radioactivity level and trace element content of the sediment samples from the North-Western Niger Delta Oil province could constitute health hazard to occupationally exposed workers, and to the public if not properly disposed. However, despite the careful disposal practice claims by the Oil industries, and given the high concentrations, the sediments could still pose an intrinsic health hazard considering their cumulative effects in the environment.     

Ion Chromatographic Determination of Traces of Sodium,Magnesium and Chlorine in Gadolinium Nitrate

Abstract

Two independent and sensitive ion chromatographic methods with suppressed conductivity were developed for determination of traces of Cl, Na, and Mg in gadolinium-nitrate. Na-Mg was determined by cation-exchange column after matrix separation, whereas Cl was analyzed without matrix separation by high capacity anion-exchange column. Detection limit for Cl was 0.01 µg mL^?1 in sample solution and 1 µg g^?1 in solid sample. The reproducibility (100 µL injected) was better than 3%, 3% and 4% at 50, 25 and 50 µg L^?1 level for Cl, Na, and Mg respectively. The overall precision was better than ±7% for Na-Mg and ±5% for Cl.     

Synthesis, spectral studies and complexation properties of N,N′-bis(5-bromo-salicylidene)-2-hydroxy-1,3-propanediamine (BSHP) and iron extraction with BSHP from oils

A Schiff base was synthesized by reaction of 1,3-diamino-2-propanol and 5-bromo-2-hydroxy benzaldehyde. The Schiff base N,N′-bis(5-bromo-salicylidene)-2-hydroxy-1,3-propanediamine (BSHP) was characterized by elemental analysis, ¹H NMR, ¹³C NMR, IR, UV-Vis spectral studies. The complexation of iron with BSHP was investigated spectrophotometrically. The extraction of iron from oil phase to aqueous phase was carried out with BSHP. Extraction conditions were optimized using central composite design. Optimum extraction conditions were found to be 32°C, 2 mL/g for the ratio of the volume of the Schiff base solution to the amount of oil, and 11 min for the stirring time. The method has been validated by using oil based metal standard, obtaining satisfactory results. The limit of detection (LOD) of the improved method is 0.04 μg/g. It has been applied to analysis of different oil samples. The concentrations of iron in olive, sunflower and corn oils were found to be 0.65 ± 0.02, 0.41 ± 0.01, 0.36 ± 0.03 μg/g, respectively. A simple, cheap, rapid, efficient, sensitive and accurate alternative analytical method for the iron determination in oils has been presented in this paper.     

Soil and Leaf Nutrients Drivers on the Chemical Composition of the Essential Oil of Siparuna muricata (Ruiz & Pav.) A. DC. from Ecuador

Chemical compositions of plants are affected by the initial nutrient contents in the soil and climatic conditions; thus, we analyzed for the first time the effects of soil and leaf nutrients on the compositions of the essential oils (EOs) of Siparuna muricata in four different localities in Ecuador. EOs were obtained by hydrodistillation and analyzed by gas chromatography/mass spectrometry (GC/MS) and a gas chromatography/flame ionization detector (GC/FID). Enantiomeric distribution by GC/MS was determined, modifying the enantiomeric separation of β-pinene, limonene, δ-elemene, β-bourbonene, cis-cadina-1 (6), 4-diene and atractylone. A total of 44 compounds were identified. The most representative for L1 were guaiol, atractylone and 4-diene; for L2, cis-cadina-1(6),4-diene and myrcene; for L3, atractylone, myrcene and germacrene B; and finally, L4 germacrene B, myrcene and cis-cadina-1(6),4-diene. Correlations between soil- leaf chemical elements such as Al, Ca, Fe, Mg, Mn, N and Si in the different localities were significant with chemical composition of the essential oil of Siparuna muricata; however, correlations between soil and leaf K, P, and Na were not significant. Cluster and NMDS analysis showed high dissimilarity values of secondary metabolites between four localities related with changes in soil- leaf nutrients. Thus, the SIMPER routine revealed that not all secondary metabolites contribute equally to establishing the differences in the four localities, and the largest contributions are due to differences in guaiol, cis-cadina-1(6),4-diene, atractylone and germacrene. Our investigation showed for the first time the influences of altitude and soil- leaf chemical elements in the chemical composition of the EOs of S. muricata.