Gas Chromatography Coupled To Mass Spectrometry Research Articles

The aim of this findings was to evaluate the effect of Trichoderma asperellum (It-13) as bio-control agent against Rhizopus stolonifer the causative agent of yam tuber rot. The antagonism test was done by dual culture on Potato Dextrose Agar (PDA). Antibiosis was evaluated on PDA medium by the cellophane membrane method. The production of lytic enzymes (chitinase, cellulase, protease, and lipase) by T. asperellum was detected on PDA supplemented with specific substract. The organic extract was obtained by fermentation of T. asperellum on Potato Dextrose Broth. Total phenols and flavonoids were by spectrophotometer while, Volatile Organic Compounds (VOC) were analysed by Gas Chromatography coupled with Mass Spectrometry (GC-MS). The efficiency of the organic extract on Rhizopus stolonifer was evaluated by poisoning method. The ability of the antagonist to protect yam tuber was done before and after infected the tubers. The results showed that, in dual culture, T. asperellum significantly inhibited the growth of the Rhizopus stolonifer at 48.68 % and 96.42% respectively, in the same media and after growth on cellophane membrane. In the specific solid media, T. asperellum produced chitinase (58.7mm), cellulase (53.8mm), protease (70.0mm) and lipase (50.7mm). The organic extract produced by this strain content total phenol (70.0mg/ml) and flavonoid (30.0mg/ml). The GC-MS analysis of VOC reveal the presence of 17 components with 6-β-hydroxyfluoxymesterone (23.32%), 2-[5-chloro-8-hydroxy-3-methyl-1-oxoisochroman-7-carbonyl) amino]-3-phenyl propionate (18.44%) and acid-2-chloro-5-sulfoaniline (12.02%) as major components. At 75μg/μl, the organic extract had total inhibited (100%) the mycelial growth of Rhizopus stolonifer while, at 107conidia/ml, the spore of T. asperellum (It-13) significantly reduced the necrosis of yam tuber at 25% and 100% respectively, before and after infection with R. stolonifer. These works suggested that the use of Trichoderma asperellum could be serve as alternative to bio-control against post-harvest rot of the yam tubers.

ABSTRACT Forest species are characterized by their wealth of essential oils (EOs), which play key requested for alternative control methods against weeds, fungi and pests. This study reports the chemical composition and highlight the antioxidant, antifungal and phytotoxic properties of the EOs obtained from Eucalyptus populifolia Desf, Eucalyptus woollsiana and Eucalyptus exserta. The EOs were analyzed by gas chromatography coupled to mass spectrometry (GC/MS). Their antioxidant, antifungal and phytotoxic properties were investigated. All EOs displayed a specific richness in eucalyptol (75.94-7.01%), camphene (6.97-0.4%) globulol (5.20-5.83%) and α-pinene (0.71-12.82 %). EOs isolated from E. populifolia exhibited significant antioxidant activity. Furthermore, all investigated EOs displayed significant antifungal properties against four phytopathogenic fungi belonging to Fusarium genus. The phytotoxic activity against five weeds showed varying effectiveness on seed germination and seedling growth, which exhibited greater effectiveness compared to glyphosate. Eucalyptus EOs have the potential to be used in the formulation of biopesticides.

Background/Objective: Wyethia amplexicaulis (shiny mule's ears) and Wyethia helianthoides (white-head mule's ears) are conspicuous forbs growing in open hillsides and prairies at mid to upper elevations in the Intermountain West region of the United States. There have been no previous reports on the essential oil compositions of any Wyethia species, so the objective of this study is to examine the chemical compositions, including enantiomeric distribution of chiral terpenoids, of W. amplexicaulis and W. helianthoides from southern Idaho. Methods: Three individual samples of W. amplexicaulis and W. helianthoides were collected, and the essential oils were obtained by hydrodistillation using a Likens-Nickerson apparatus and analyzed by gas chromatography coupled with mass spectrometry (GC-MS), gas chromatography with flame ionization detection, and enantioselective GC-MS. Results: The essential oils were obtained in yields of 0.090% to 0.136% and 1.489% to 1.771% for W. amplexicaulis and W. helianthoides, respectively. The three W. helianthoides samples showed high similarity with (−)-germacrene D (16.5%-21.5%), ( E)-β-ocimene (10.0%-14.3%), myrcene (8.6%-12.4%), α-pinene (6.3%-7.3%, ≥ 95% (+)-α-pinene), 15-copaenol (4.3%-6.0%), and carotol (3.5%-5.9%) as the major components. The W. amplexicaulis essential oils, on the other hand, showed variation. Two samples were rich in monoterpene hydrocarbons, mostly myrcene (22.4% and 32.2%), while the third sample was dominated by oxygenated sesquiterpenoids, 15-copaenol (11.4%), carotol (10.0%), silphiperolan-7β-ol (8.2%), and caryophyllene oxide (5.8%). This is the first investigation of Wyethia essential oils. Conclusions: There are 11 recognized Wyethia species, so additional research is needed to understand the volatile phytochemicals present in this genus.

Illicit drug use is a serious and complex public health problem, not only due to the severity of the health damage but also to the social implications, such as marginalization and drug trafficking. Currently, cocaine (COC) is among the most abused drugs worldwide with about 22 million users. Drug abuse has also been found in women during the pregnancy period, which has shed light on a new group for epidemiology. The diagnosis of COC use in these cases usually depends largely on the mother's reports, which in several cases omit or deny consumption. Therefore, considering physical-chemical methods of sample preparation and exposure biomarkers, the development of analytic toxicological methods can help to confirm drug use during pregnancy. Thus, the objective of the present work was to develop an analytical method based on dispersive liquid-liquid microextraction for the determination of COC analytes, using umbilical cord tissue as an alternative biological matrix, and detection by gas chromatography coupled to mass spectrometry. Therefore, after optimization, the dispersive liquid-liquid microextraction method was fully validated for quantification of COC, benzoylecgonine, cocaethylene, ecgonine, ecgonine methyl ester and norcocaine. The limits of detection were between 15 and 25 ng/g, the limits of quantification were 30 ng/g for ecgonine and 25 ng/g for the other analytes. Linearity ranged from the limits of quantification to 1,000 ng/g. Coefficients of variation for intra-assay precision were <18.5%, inter-assay was <8.75% and bias was <16.4% for all controls. The developed method was applied in 10 suspected positive samples, based on the mother's report and maternal urine screening and confirmation. COC, benzoylecgonine, ecgonine and ecgonine methyl ester were quantified in four umbilical cords with concentrations that ranged from 39.6 to 420.5 ng/g.

Research on new plant-based insecticides meets the need for an alternative to address mosquito resistance to synthetic insecticides. This study assessed the adulticidal activity and synergistic effects of essential oils (EOs) from Citrus aurantiifolia peels and Hyptis spicigera leaves on female adults of Anopheles gambiae s.l. The extraction yields were on the order of 0.17 and 0.11%, respectively, for C. aurantiifolia and H. Spicigera EOs obtained by hydrodistillation. The phytochemical composition of the EOs was analysed by Gas Chromatography coupled with Mass Spectrometry (GC-MS). GC-MS revealed that the essential oils of C. aurantiifolia and H. spicigera contained high amounts of monoterpene compounds (100% and 77.45%, respectively). Adulticidal activity was assessed using WHO and CDC bottle bioassays at concentrations of 2.5, 5, 7.5 and 10 mg/ml/btl. The EOs of both plants caused significant concentration-dependent Knock down and adulticidal activities. Individually, H. spicigera EOs had more adulticidal effects (LC50 = 4.42 mg/ml/btl) than did C. aurantiifolia EOs (LC50 = 6.79 mg/ml/btl). An EO mixture 25%Ca + 75%Hs from C. aurantiifolia and H. spicigera had synergistic effects (CI = 142.84; SF = 1.42) on female Anopheles gambiae adults. Combinations of the two plant EOs considerably optimize their insecticidal effectiveness.

Our research focuses on exploring the chemical composition and some biological properties of the essential oil derived from Syzygiella rubricaulis (Nees) Stephani, a bryophyte species. To conduct a comprehensive analysis, we utilized a DB5MS capillary column along with gas chromatography coupled to mass spectrometry (GC-MS) and flame ionization (GC-FID). The qualitative and quantitative examination revealed the presence of 50 compounds, with hydrocarbon sesquiterpenes (48.35%) and oxygenated sesquiterpenes (46.89%) being the predominant constituents. Noteworthy compounds identified include bicyclogermacrene (12.004%), cedranone <5-> (9.034%), spathulenol (6.835%), viridiflorol (6.334%), silphiperfol-5,7(14)-diene (6.216%), biotol <β-> (6.075%), guaiol (4.607%), viridiflorene (4.65%), and α-guaienol (3.883%). Furthermore, we assessed the antimicrobial, antioxidant, and anticholinesterase activity of the essential oil, revealing a compelling inhibitory effect against acetylcholinesterase (AChE) with an IC50 value of 26.75 ± 1.03 µg/mL and a moderate antimicrobial (MIC 500 µg/mL, Enterococcus faecium, Lysteria monocytogenes) and antioxidant effect (ABTS: SC50 343.38 and DPPH 2650.23 µg/mL). These findings suggest the potential therapeutic application of the bryophyte essential oil in the treatment of Alzheimer's disease due to its potent anticholinesterase properties.

The Myrtaceae family plays a significant role in the Angiosperm landscape in Brazil, standing out as one of the most relevant. Within this context, the genus Myrcia ranks as the fourth largest, and its plant extracts and essential oils from these species are recognized as a valuable source of plant bioactives. In this context, Myrcia glomerata, popularly known as guamirim, stands out. Despite belonging to the Myrtaceae family, there is a lack of detailed research on its biological activities and chemical composition. The phytochemical investigation of the different plant extracts: ethanolic (EE), methanolic (ME), hexane (HE), acetone (AE), ethyl acetate (EAE) and dichloromethane (DE) revealed the presence of saponins, free steroids, alkaloids, anthocyanins, anthocyanidins, flavones, flavonols, xanthones, chalcones, aurones, flavononols and tannins, leading to the quantification of phenolic compounds (flavonoids, tannins, and alkaloids). The essential oil of the leaves, identified by gas chromatography coupled to mass spectrometry (GC-MS) identified 29 compounds, corresponding to 97.54% of the total area of the essential oil of M. glomerata. The main compounds found were sesquiterpenes, Elemicin (76.85%), Elixene (3.99%), E-caryophyllene (2.25%). EE showed the best antimicrobial potential, with concentrations ranging from 0.39 to 25 mg.mL-1, with Staphylococcus aureus and Proteus mirabilis strains being more susceptible in EE, ME and AE, showing 98.72%, 96.23% and 88.60% antioxidant activity, respectively. As for the antibiofilm potential, ME showed the greatest biomass reduction (90.53%) for Salmonella enterica Typhimurium, with cell viability of 9.02%. These results demonstrate the potential of EE and ME extracts from M. glomerata, representing a possible source of natural bioactives to be used in pharmaceuticals for the control of resistant microorganisms.

IntroductionPreviously, we documented that the malaria vector Anopheles gambiae responds to volatile emissions from the root exudate water of the invasive plant, Parthenium hysterophorus. However, the origin of the volatiles remains to be investigated. Here, we isolated bacteria from the root exudate water of the plant, test the influence of their volatiles in gravid An. gambiae oviposition, and examined relationships between volatile profiles and oviposition.MethodsBacteria from root exudate water of P. hysterophorus were isolated using culture on Luria Bertani medium and identified by sequencing the 16S rRNA gene. Cultures of individual isolates were evaluated for egg laying response by gravid An. gambiae and number of eggs laid compared using generalized linear models relative to those in crude bacteria-mixture. Headspace volatile emissions of the bacterial isolates were analyzed by gas chromatography coupled to mass spectrometry (GC-MS) and relationships between volatile organic compound (VOC) profiles and gravid mosquito oviposition examined using Random Forest Analysis. Proximate analysis was performed to assess the difference in volatile chemistry among the different isolates.ResultsThree isolates were identified as Gram-negative bacteria belonging to two families: Enterobacteriaceae (Enterobacter sp. and Enterobacter mori) and Alcaligenaceae (Alcaligens aquatilis). An. gambiae laid 3-fold more eggs in cultures of A. aquatilis than in those of Enterobacter sp. In turn, approx. 4-fold more eggs were laid in cultures of E. mori than A. aquatilis. Overall, 16 VOCs were identified in the headspace of the isolates belonging to the chemical classes benzenoids, pyrazines, aldehydes, terpenes, alcohols, alkanes, and indoles. Random Forest Analysis identified 10 compounds contributing the most to the attraction of odors of the bacteria isolates to oviposition. Specifically, dodecane and indole were emitted in higher amounts in odors of Enterobacter sp than the other two species. Proximate analysis revealed differential attraction of the isolates on the gravid mosquito to be associated with their volatile profiles.ConclusionOur results provide first report of E. mori or A. aquatilis mediating attractive oviposition responses in An. gambiae in support of the important role microbes play in insect oviposition. The potential use of the microbes and associated volatiles in malaria vector management needs further investigation.

Introduction. This article aims to present a simple and sensitive chromatographic method, carried out in the gas phase using detection by mass spectrometry to identify and quantify cocaine and its metabolites in the blood, notably Benzoylecgonine and Ecgonine Methyl ester. Methods. This method involves liquid-liquid extraction using a mixture of solvents, consisting of chloroform and isopropanol, followed by silylation. The separation was carried out using an xi-5ms column (Restek®) of 30 m in length, 0.25 mm in internal diameter and 25 μm in film thickness. Results. Blood level quantification of Benzoylecgonine and Methylester Ecgonine was possible with respective quantification limits of 18 and 39 ng/mL. The method is linear over a range of 75 to 1000 ng/mL and the extraction yields range between 81% and 97%. Regarding the intra- and inter-run precision and the accuracy of the method, the coefficients of variation and biases at the three concentration levels (150, 300 and 750 ng/mL) are well below 15%. This method can easily be applied to blood samples, both in emergency toxicology and in forensic toxicology, to confirm any previous, voluntary, or accidental intake of cocaine.

The cabbage aphid (Brevicoryne brassicae) is a major pest of kale (Brassica oleraceae var. acephala), an important vegetable that is grown worldwide due to its high nutritional and economic value. Brevicoryne brassicae poses a great challenge to B. oleraceae var. acephala production, causing significant direct and indirect yield losses. Farmers overly rely on synthetic insecticides to manage the pest with limited success owing to its high reproductive behavior and development of resistance. This necessitates a search for sustainable alternatives to mitigate these challenges. This study assessed behavioral responses of B. brassicae to odors from rosemary (Rosmarinus officinalis) and B. oleraceae var. acephala headspace volatiles in a Perspex four-arm olfactometer. We identified and quantified volatiles emitted by each of the two plants and those eliciting antennal response using coupled gas chromatography-mass spectrometry (GC-MS) and GC-electroantennograhic detection(GC-EAD), respectively. Our findings revealed that B. brassicae spent more time in the arms of the olfactometer that contained B. oleraceae var. acephala volatiles compared to the arm that held R. officinalis volatiles. Additionally, B. brassicae spent more time in the olfactometer arms with B. oleracea var. acephala compared to the arms holding B. oleracea var. acephala and R. officinalis enclosed together and clean air. GC-MS analysis revealed diverse and higher quantities of volatile compounds in R. officinalis compared to B. oleraceae var. acephala. GC-EAD analysis showed that antennae of B. brassicae detected Linalool, α-Terpineol, Verbenone, Geraniol, Camphor, and Borneol from the volatiles of R. officinalis, and Sabinene, γ-Terpinene, and β-Caryophyllene from B. oleraceae var. acephala volatiles.Our findings demonstrate the potential of R. officinalis as a repellent plant against B. brassicae and could be utilized as a 'push' plant in an intercropping strategy against this pest.

The present study examines for the first time the emission patterns and olfactory signatures of 9 complete human corpses of different stages of decomposition. Air sampling was performed inside the body bags with solid sorbents and analysed by coupled gas chromatography-mass spectrometry after thermal desorption (TD-GC-MS). Furthermore, odour-related substances were detected by gas chromatography-olfactometry (GC-O). Sulfurous compounds (mainly dimethyl di- and trisulfide) were identified as most important to the odour perception. Around 350 individual organic substances were detected by TD-GC-MS, notably sulfurous and nitrogenous substances as well as branched alkanes, aldehydes, ketones, alcohols, carboxylic acids, carboxylic acid esters and ethers. A range of terpenes was detected for the first time in a characteristic emission pattern over all decomposition stages. Concentrations of the substances varied greatly, and no correlation between the emission patterns, the stage of decomposition and the cause of death could be found. While previous studies often analysed pig cadavers or only parts of human tissue, the present study shows the importance of analysing complete human corpses over a range of decomposition stages. Moreover, it is shown that using body bags as a kind of “emission test chamber” is a very promising approach, also because it is a realistic application considering the usual transport and store of a body before autopsy.Graphical abstract

Comparative Metabolomic Profiling of Eggs from 3 Diverse Chicken Breeds Using GC-MS Analysis

Griffinia gardneriana Ravenna, Griffinia liboniana Morren and Griffinia nocturna Ravenna (Amarillydaceae) are bulbous plants found in tropical regions of Brazil. Our work aimed to determine the alkaloid profiles of Griffinia spp. and evaluate their anxiolytic potential through in vivo and in silico assays. The plants grown in greenhouses were dried and their ground bulbs were subjected to liquid-liquid partitions, resulting in alkaloid fractions that were analyzed by gas chromatography coupled to mass spectrometry (GC-MS). Anxiolytic activity was evaluated in zebrafish (Danio rerio) through intraperitoneal injection at doses of 40, 100 and 200 mg/kg in light-dark box test. GC-MS analyses revealed 23 alkaloids belonging to different skeleton types: lycorine, homolychorine, galanthamine, crinine, haemanthamine, montanine and narcisclasine. The chemical profiles were relatively similar, presenting 8 alkaloids common to the three species. The major component for G. gardneriana and G. liboniana was lycorine, while G. nocturna consisted mainly of anhydrolycorine. All three alkaloid fractions demonstrated anxiolytic effect. Furthermore, pre-treatment with diazepam and pizotifen drugs was able to reverse the anxiolytic action, indicating involving the GABAergic and serotonergic receptors. Molecular docking showed that the compounds vittatine, lycorine and 11,12-dehydro-2-methoxyassoanine had high affinity with both receptors, suggesting them to be responsible for the anxiolytic effect.

This work describes the antimycotic activity of propolis from the stingless bees Scaptotrigona mexicana and Tetragonisca angustula, collected from two Mexican regions (Veracruz and Chiapas, respectively), against three clinical isolates and the reference strain ATCC 14522 of Malassezia pachydermatis, the causative agent of canine otitis. The chemical components of the ethanolic extracts of propolis were determined by gas chromatography coupled with mass spectrometry (GC-MS), and sesquiterpenes were the predominant compounds. The antimycotic activity was evaluated by plate microdilution. The induced changes in the yeasts were evaluated by fluorescence microscopy and staining with calcofluor white and propidium iodide. The minimum inhibitory concentration (MIC) was 7.11 mg/mL, and the minimum fungicidal concentration was 21.33 mg/mL for both extracts. The EPPs of Scaptotrigona mexicana and Tetragonisca angustula caused substantial damage to yeast morphology, where the propidium iodide staining of the yeasts treated with both EEPs revealed the penetration of this marker, which indicates the destruction of the cell wall and plasma membrane of the fungi. This result suggests that these types of propolis could be used as alternative treatments for canine external otitis. To the best of our knowledge, this seems to be the first scientific report that has demonstrated structural damage in Malassezia pachydermatis by Mexican stingless bee propolis.

Drought induces moderate, diverse changes in the odour of grassland species

Current vector control strategies based on synthetic chemicals are not eco-friendly against non-target organisms; hence, alternative approaches are highly required. Commercially purchased oil of Mentha spicata (Spearmint) and Eucalyptus citriodora (Citriodora) were examined against the medical pest Cx. quinquefasciatus (Say) and their non-toxicity on the aquatic species was evaluated. Chemical screening with gas chromatography coupled with mass spectrometry (GC-MS) analysis revealed a total of 14 and 11 compounds in Citriodora and Spearmint oils, respectively, with the highest peak (%) at carvone (70.44%) and isopulegol (30.4%). The larvicidal activity on the fourth instar larvae of Cx. quinquefasciatus showed dose-dependent mortality and significance at a 100ppm concentration 48h post-treatment with Citriodora (76.4%, P ≤ 0.001) and Spearmint (100%, P ≤ 0.001). Additionally, the photomicrograph of the fourth instar larvae revealed significant physical abnormalities in the head and midgut tissues post-exposure to Spearmint and Citriodora oils. Moreover, the histological assay revealed severe damage in the epithelial cells and gut lumen 2 to 24h post-treatment. The repellency percentage of adult Culex mosquitoes was prominent across both oils at 150ppm 210min post-exposure. Non-target toxicity on the aquatic predator showed both essential oils (Spearmint oil (17.2%) and Citriodora oil (15.2%)) are safer at the maximum treatment (200ppm) compared to temephos (75.4% at 1ppm). The in silico screening of phyto-compounds derived by both essential oils with BeeTox (online server) showed no contact toxicity to the honey bee Apis mellifera. Overall, the present research revealed that Spearmint and Citriodora essential oils and their active phyto-compounds were toxic to Cx. quinquefasciatus and harmless to the aquatic predator and honey bee.

According to green analytical chemistry principles, the use of agricultural byproducts as sorbent phases is an interesting topic due to their lignocellulosic origin, as they are biodegradable and inexpensive. To the best of our knowledge, this is the first study in which avocado seed and avocado seed activated carbon are proposed as sustainable sorbents for solid-phase microextraction technologies, which were used to assess the proof of concept. Rotating disk sorptive extraction (RDSE) was used as a model technology and ibuprofen (Ibu) and 1-hydroxy-ibuprofen (1-OH-Ibu) as representative analytes. It was found that activated carbon (AC) prepared at 600°C with an impregnation ratio (raw material/activating agent (ZnCl2), w/w) of 1:1.2 had better extraction efficiency than other ACs obtained at different temperatures, impregnation ratios, and activating agents (K2CO3). Characterization revealed several differences between natural avocado seed, biochar prepared at 600°C, and selected AC since the typical functional groups of the natural starting material begin to disappear with pyrolysis and increasing the surface area and pore volume, suggesting that the main interactions between analytes and the sorbent material are pore filling and π-π stacking. By using this AC as the sorbent phase, the optimal extraction conditions in RDSE were as follows: the use of 50mg of sorbent in the disk, 30mL of sample volume, pH 4, 90min of extraction time at a rotation velocity of the disk of 2000rpm, and methanol as the elution solvent. The extracts were analyzed via gas chromatography coupled to mass spectrometry (GC-MS). The method provided limits of detection of 0.23 and 0.07µg L-1 and recoveries of 81% and 91% for Ibu and 1-OH-Ibu, respectively. When comparing the extraction efficiency of the selected activated carbon with those provided by Oasis® HLB and C18 in RDSE, nonsignificant differences were observed, indicating that avocado seed activated carbon is a suitable alternative to these commercial materials.

Chemical composition, antimicrobial activity, and antioxidant capacity of Micromeria flagellaris Baker and M. madagascariensis Baker: Two endemic species from Madagascar as sources of essential oils

The development of selective extraction protocols for Cannabis-inflorescence constituents is still a significant challenge. The characteristic Cannabis fragrance can be mainly ascribed to monoterpenes, sesquiterpenes and oxygenated terpenoids. This work investigates the entrapment of Cannabis terpenes in olive oil from inflorescences via stripping under mild vacuum during the rapid microwave-assisted decarboxylation of cannabinoids (MW, 120 °C, 30 min) and after subsequent extraction of cannabinoids (60 and 100 °C). The profiles of the volatiles collected in the oil samples before and after the extraction step were evaluated using static headspace solid-phase microextraction (HS-SPME), followed by gas chromatography coupled to mass spectrometry (GC-MS). Between the three fractions obtained, the first shows the highest volatile content (~37,400 mg/kg oil), with α-pinene, β-pinene, β-myrcene, limonene and trans-β-caryophyllene as the main components. The MW-assisted extraction at 60 and 100 °C of inflorescences using the collected oil fractions allowed an increase of 70% and 86% of total terpene content, respectively. Considering the initial terpene amount of 91,324.7 ± 2774.4 mg/kg dry inflorescences, the percentage of recovery after decarboxylation was close to 58% (mainly monoterpenes), while it reached nearly 100% (including sesquiterpenes) after extraction. The selective and efficient extraction of volatile compounds, while avoiding direct contact between the matrix and extraction solvents, paves the way for specific applications in various aromatic plants. In this context, aromatized extracts can be employed to create innovative Cannabis-based products within the hemp processing industry, as well as in perfumery, cosmetics, dietary supplements, food, and the pharmaceutical industry.

Calling males of Anastrepha obliqua release volatile compounds to attract conspecific males to form leks and females to mate. Male volatiles from Mexican and Brazilian populations of A. obliqua have been previously identified. However, there are differences in the number and identity of volatile compounds between the populations. These differences in volatile profiles may be due to male origin (e.g. wild or mass-reared flies) or methodological issues (e.g. sampling techniques). In this study, we evaluated the attractiveness of wild, laboratory non-irradiated, and laboratory-irradiated flies under semi-field conditions. Male volatiles were collected using dynamic headspace sampling (DHS) and solid-phase microextraction (SPME) techniques, and identified using gas chromatography-coupled mass spectrometry. The results showed no difference in the attractiveness of wild, laboratory non-irradiated, and irradiated males to females. However, the number of captured females differed according to the origin; wild and non-irradiated females were captured more frequently than the irradiated flies. A total of 21 compounds were found using SPME, whereas only 12 were collected using DHS, although the relative amounts of these compounds were higher than those obtained using the former sampling technique. In addition, only laboratory non-irradiated males released α-pinene and menthol, which have not been previously reported in this fruit fly species. Additionally, we identified novel compounds in A. obliqua; however, certain compounds previously reported were not detected. This study suggests that despite the qualitative and quantitative variations in the volatile profiles of A. obliqua males, their attractiveness was unaffected.