29 research outputs found

    Distillation methods affect the chemical composition of Varronia curassavica Jacq, essential oil?

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    The objective of this work was to evaluate the chemical composition of essential oil from Varronia curassavica Jacq. obtained by microwave (MI) and hydrodistillation (HD) extraction methods. The MI method tested three powers (500, 600, and 700W), three distillation times (20, 30, and 40 min.), and three water volumes (0, 25, and 50 mL per sample). The HD method tested three distillation times (100, 120, and 140 min.) and three water volumes (1.0, 1.5, and 2.0 L per 3-liter flask). The essential oils were analyzed by GC/MS-FID. The optimal condition for the essential oil extraction by the MI method was 700W for 40 min. (3.28%), regardless of the volume of water. In its turn, the best condition for essential oil extraction by the HD method was 120 min. with 1.0 L of water per flask (3.34%). The most abundant compounds for MI (700 W for 40 min. without water) were shyobunol (26.53%) and bicyclogermacrene (4.96%); and the most abundant compounds for HD (120 min. with 1.0 L of water/flask) were shyobunol (24.00%) and germacrene D-4-ol (10.23%). Methyl farnesoate (2E, 6E) and farnesyl acetate (2Z, 6E) were not detected in the essential oil extracted by HD; however, they were identified by the MI method. By increasing the distillation time and/or volume of water in HD, a reduction was observed for the content of the chemical compounds -elemene (from 1.23 to 0.97%), Ecaryophyllene (from 5.49 to 4.35%), -humulene (from 1.80 to 1.43%), alloaromadendrene (from 1.78 to 1.44%), bicyclogermacrene (from 5.63 to 4.55%), and germacrene D-4-ol (from 11.40 to 9.86%). Power, extraction time, and their interactions influenced the content of essential oil obtained by microwave extraction (MI). Within each power, the highest essential oil content was extracted at the longest distillation time (40 min.), except for 600W, where no significant difference was detected between 30 and 40 min. The optimal essential oil contents for both extraction methods were statically similar by the t-test for dependent samples. However, the MI method presents advantages, such as shorter distillation time and less energy and water consumption

    Toxicity and repellency of the essential oil from Lippia gracilis to the coconut mite Aceria guerreronis (Acari: Eriophyidae).

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    The essential oil (EO) from different genotypes of Lippia gracilis Schauer (Verbenaceae) present two distinctive chemotypes containing either thymol or its isomer carvacrol as major compounds, both of which have proven bioactivity against several agricultural pests. Recently, we have shown that L. gracilis accession LGRA 106 and its major compound thymol are toxic and repellent against the coconut mite, Aceria guerreronis Keifer (Acari: Eriophyidae), a key pest of coconut plantations in Asia, Africa and America. Since intraspecific variation affects the chemical composition of EO and hence, its bioactivity, here we assessed the acaricidal and repellent effects of L. gracilis accession LGRA109 to A. guerreronis. Leaves of this accession contain carvacrol (49.35%) as major compound. The LC50 of the EO and of carvacrol estimated for A. guerreronis were 28.01 and 6.84 mg/mL, respectively. Carvacrol, at its LC50, as well as the EO and carvacrol at their LC99, repelled the mite. Our results indicated that carvacrol and the EO of L. gracilis accession LGRA109 were bioactive against A. guerreronis; however, the EO was less effective than its major compound

    Análise molecular via ISSR de uma população nativa de Eplingiella fruticosa.

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    Edição Especial dos Anais do 3° Simpósio da Rede de Recursos Genéticos Vegetais do Nordeste, Aracaju, out. 2017
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