Abstract Butia capitata, native to the Brazilian cerrado, is underutilized for human consumption. The objective was to determine the physical characteristics of the fruit, centesimal composition, bioactive and antioxidant activity. Fruits obtained in Montes Claros, Minas Gerais, Brazil. Diameter, height and weight were evaluated. The moisture was analyzed by gravimetry after oven drying, ashes by calcining in a muffle furnace, proteins by the Kjeldahl method, gravimetric lipids after extraction in ethyl ether, carbohydrates by difference and total energy value by conversion factors. Vitamin C, E and carotenoids were analyzed by HPLC, minerals by inductively coupled plasma atomic absorption spectrometry, Folin Ciocalteu solution phenolic compounds, anthocyanins by spectrophotometry and antioxidant capacity by the Radical DPPH. The fruits presented good pulp yield (68.59%), which has a high lipid content (3.42 g.100 g-1) and total energy (83.34 kcal.100 g-1). The pulp contains ß-carotene (8.56 mg.100 g-1), vitamin E (121.07 mcg.100 g-1) and high concentrations of vitamin C (53.57 mg.100 g-1), total phenolics (493, 6 mg.100 g-1) and copper (1.80 mg.100 g-1). Almond has a high value of total energy (457.72 kcal.100 g-1), vitamin E (1594.39 mcg.100 g-1) and minerals Cu (2.40 mg.100 g-1) and Mo (0.9.100 g-1). The pulp is a source of carotenoids, vitamin C, copper and total phenolics, both natural antioxidants.

RESUMO: Existem fatores que podem afetar o conteúdo de óleo essencial das plantas, sendo o horário de coleta um deles. Assim, observa-se que o teor e a composição química de óleo essencial podem variar em certas plantas de acordo com horário de coleta. O objetivo deste trabalho foi avaliar o efeito do horário de coleta sobre o conteúdo e a composição química do óleo essencial das folhas de goiabeira ( Psidium guajava ). Folhas de Psidium guajava foram coletadas em diferentes horários do dia para determinar teor e composição química de seu óleo essencial. O óleo essencial não apresentou variação qualitativa da composição química em relação ao horário de coleta das folhas de Psidium guajava , mas alterou a concentração das substâncias, entre elas o α-humuleno e o trans-cariofileno. Os constituintes principais do óleo essencial das folhas de Psidium guajava são o limoneno (2,2-4,4%), trans-cariofileno (18,1-17,1%), α-humuleno (26,3-20,4%), aromadendreno (7,6-12,2%), α-selineno (7,3-11,3%), óxido de cariofileno (3,7-3,3%) epóxido de humuleno II (4,1-1,9%) e o selin-11-en-4α-ol (7,2-11,1%). No entanto, a maior produção de óleo essencial, foi obtida com as folhas coletadas às 19h, apresentando conteúdo de 0,38% (b.s.) e a mais baixa produção às 07h, apresentando conteúdo de 0,24% (b.s.). Através da análise química, identificou-se que compostos sesquiterpênicos apresentaram uma maior concentração (62,0%) e os monoterpenos e monoterpenoides foram os que apresentaram menor concentração (2,2 e 1,1%, respectivamente). As classes que sofreram maiores mudanças em relação ao horário de coleta foram os monoterpenos (2,2-4,4%) e os sesquiterpenos e os sesquiterpenoides (63,8-61,7% e 15,9-13,2%, respectivamente).

ABSTRACT: The essential oil plants contents can be affected by several factors. For example, in certain plants, collection time has been observed to affect the content and chemical composition of the essential oil obtained from the plant. The objective of this study was to evaluate the effect of collection time on the content and chemical composition of the essential oil from guava ( Psidium guajava L.) leaves. Leaves were collected at different times of the day and the content and chemical composition of their essential oil was determined. Collection time did not qualitatively affect the chemical composition of the essential oil. However, concentration of certain substances in the oil, such as α-humulene and trans-caryophyllene, did significantly vary at different collection times. The main constituents of the essential oil of Psidium guajava are limonene (2.2-4.4%), trans-caryophyllene (18.1-17.1%), α-humulene (26.3-20.4%), aromadendrene (7.6-12.2%), α-selinene (7.3-11.3%), caryophyllene oxide (3.7-3.3%), humulene epoxide II (4.1-1.9%), and selin-11-en-4α-ol (7.2-11.1%). Leaves collected at 7:00 AM had higher essential oil production, with a content of 0.38% (d.b.), whereas leaves collected at 7:00 PM had lower essential oil production, 0.24% (d.b.). Chemical analysis showed that sesquiterpene compounds represented the highest concentration (62.0%), and monoterpenoids and monoterpenes represented the lowest concentrations (1.1 and 2.2%, respectively). Chemical classes that underwent major changes with respect to collection time were monoterpenes, sesquiterpenes, and sesquiterpenoids (2.2-4.4%, 63.8-61.7%, and 15.9-13.2%, respectively).

A bioassay-guided fractionation of culture filtrates of the fungus Alternaria euphorbiicola, a pathogen of the weed Euphorbia heterophylla, led to the isolation of anhydromevalonolactone (1), tyrosol (2), (R)-( - )-mevalonolactone (3), and cycloglycylproline (4). When tested on the punctured leaves of the host plant, these compounds produced bleached lesions with dark brown margins at concentrations as low as 80 µM. When tested on the leaves of other relevant weeds, only cycloglycylproline showed selective activity against E. heterophylla. This is the first report on the isolation of phytotoxins from A. euphorbiicola and on the phytotoxicity of anhydromevalonolactone, (R)-( - )-mevalonolactone, and cycloglycylproline.

O objetivo deste trabalho foi avaliar a influência da adubação orgânica sobre o teor e a composição do óleo essencial de capim citronela (Cymbopogon nardus), bem como a fungitoxicidade desse óleo ao crescimento micelial dos fungos Didymella bryoniae, Colletotrichum gloeosporioides e Amphobotrys ricini. A extração do óleo essencial foi realizada por hidrodestilação, a partir de plantas cultivadas em quatro doses de adubação orgânica (0, 3, 6 e 9 kg de esterco bovino curtido por cova), e a identificação dos constituintes químicos foi conduzida por cromatografia gasosa/espectrometria de massas. Para avaliar a inibição do crescimento micelial, o experimento foi instalado no delineamento inteiramente casualizado, em arranjo fatorial. Foram testadas sete alíquotas do óleo essencial (0, 5, 10, 15, 20, 25 e 30 µL), em cinco épocas de avaliação, com quatro repetições. O teor de óleo essencial do capim citronela não foi afetado pela adubação orgânica, e o óleo essencial do capim citronela apresentou 24 compostos químicos, entre estes monoterpenos e sesquiterpenos, com maior concentração dos compostos citronelal, β-citronelol, geraniol e elemol. O óleo essencial do capim citronela apresenta maior efeito de inibição a Amphobotrys ricini, em comparação aos fungos Didymella bryoniae e Colletotrichum gloeosporioides.

The objective of this work was to evaluate the influence of organic fertilization on the content and composition of the essential oil of citronella grass (Cymbopogon nardus), as well as to assess the fungitoxicity of this oil to the mycelial growth of the fungi Didymella bryoniae, Colletotrichum gloeosporioides, and Amphobotrys ricini. The extraction of the essential oil was done by hydrodistillation in plants cultivated with four doses of organic fertilizer (0, 3, 6, and 9 kg matured cattle manure per hole), and the identification of the chemical compounds was done by gas chromatography/mass spectroscopy. To evaluate the inhibition of mycelial growth, the experiment was installed in a completely randomized design in a factorial arrangement. Seven aliquots of essential oil were tested (0, 5, 10, 15, 20, 25, and 30 µL) in five evaluating times, with four replicates. The contents of the essencial oil in citronella grass were note affected by organic fertilization, and the oil includes 24 chemical compounds, among these monoterpenes and sesquiterpenes, with higher concentrations of the compounds citronellal, β-citronellol, geraniol, and elemol. The essential oil of citronella grass has higher inhibition effect on Amphobotrys ricini, when compared to the fungi Didymella bryoniae e Colletotrichum gloeosporioides.

Objetivou-se, com este trabalho, avaliar o efeito da temperatura do ar de secagem sobre a qualidade do óleo essencial de folhas de tomilho. Foram empregadas diferentes temperaturas de secagem (30, 40, 50, 60, 70 ºC), em um secador com resistências elétricas. Os componentes químicos do óleo essencial, depois de realizada a secagem, foram comparados com os valores obtidos na planta in natura (testemunha). Para a extração do óleo essencial, foi empregado o método de extração com CO2 supercrítico. A identificação dos componentes químicos do óleo essencial foi realizada por cromatografia gasosa, acoplada ao espectrofotômetro de massas (CG-EM) e, para a quantificação desses componentes, empregou-se o cromatógrafo a gás, acoplado ao detector por ionização de chamas (CG-DIC). Em função dos resultados obtidos, recomenda-se ar, à temperatura de 60 ºC, para a secagem das folhas de tomilho.

The study aimed to evaluate the effect of drying air temperature on the quality of the essential oil from thyme leaves. Different drying temperatures (30, 40, 50, 60, 70 ºC) were applied in a dryer with electrical resistance heater. After drying, the chemical components of the essential oil were compared with those obtained from fresh samples (control). The extraction of the essential oil was performed using the supercritical CO2 method. The identification of the essential oil components was carried out by gas chromatography coupled to mass spectrometry (GC-MS) and the quantification by gas chromatography coupled to a flame ionization detector (GC-FID). According to the results, it is recommended the drying air temperature of 60 ºC for drying thyme leaves .

Multivariate models were developed using Artificial Neural Network (ANN) and Least Square - Support Vector Machines (LS-SVM) for estimating lignin siringyl/guaiacyl ratio and the contents of cellulose, hemicelluloses and lignin in eucalyptus wood by pyrolysis associated to gaseous chromatography and mass spectrometry (Py-GC/MS). The results obtained by two calibration methods were in agreement with those of reference methods. However a comparison indicated that the LS-SVM model presented better predictive capacity for the cellulose and lignin contents, while the ANN model presented was more adequate for estimating the hemicelluloses content and lignin siringyl/guaiacyl ratio.

O objetivo deste trabalho foi selecionar plantas com atividade inseticida, para isolar, identificar e avaliar a bioatividade de compostos inseticidas presentes nessas plantas, contra as seguintes pragas de produtos armazenados da ordem Coleoptera: Sitophilus zeamais Mots. (Curculionidae), Rhyzopertha dominica F. (Bostrichidae) e Oryzaephilus surinamensis L. (Silvanidae). As espécies de plantas usadas foram: anis (Ocimum selloi Benth), arruda (Ruta graveolens L.), cordão-de-frade (Leonotis nepetifolia L.), datura (Datura stramonium L.), erva baleeira (Cordia verbenacea L.), hortelã (Mentha piperita L.), melão-de-são-caetano (Mormodica charantia L.) e mentrasto (Ageratum conyzoides L.). Avaliou-se a toxicidade dos extratos hexânico e etanólico dessas plantas sobre R. dominica. Somente o extrato hexânico de A. conyzoides apresentou atividade inseticida. O extrato hexânico desta planta foi fracionado, sucessivamente, por cromatografia de coluna de sílica gel, para isolamento e purificação dos compostos ativos. Os compostos 5,6,7,8,3',4',5'-heptametoxiflavona; 5,6,7,8,3'-pentametoxi-4',5'-metilenodioxiflavona e cumarina foram identificados. Entretanto, somente a cumarina apresentou atividade inseticida às três espécies de insetos (DL50 de 2,72 a 39,71 mg g-1 de i.a.). A ordem crescente de suscetibilidade à cumarina foi R. dominica, S. zeamais e O. surinamensis.

The objective of this work was to screen plants with insecticide activity, in order to isolate, identify and assess the bioactivity of insecticide compounds present in these plants, against Coleoptera pests of stored products: Oryzaephilus surinamensis L. (Silvanidae), Rhyzopertha dominica F. (Bostrichidae) and Sitophilus zeamais Mots. (Curculionidae). The plant species used were: basil (Ocimum selloi Benth.), rue (Ruta graveolens L.), lion's ear (Leonotis nepetifolia (L.) R.Br.), jimson weed (Datura stramonium L.), baleeira herb (Cordia verbenacea L.), mint (Mentha piperita L.), wild balsam apple (Mormodica charantia L.), and billy goat weed or mentrasto (Ageratum conyzoides L.). The insecticide activity of hexane and ethanol extracts from those plants on R. dominica was evaluated. Among them, only hexane extract of A. conyzoides showed insecticide activity; the hexane extract of this species was successively fractionated by silica gel column chromatography, for isolation and purification of the active compounds. Compounds 5,6,7,8,3',4',5'-heptamethoxyflavone; 5,6,7,8,3'-pentamethoxy-4',5'-methilenedioxyflavone and coumarin were identified. However, only coumarin showed insecticide activity against three insect pests (LD50 from 2.72 to 39.71 mg g-1 a.i.). The increasing order of insects susceptibility to coumarin was R. dominica, S. zeamais and O. surinamensis.

This study was performed to establish the correlation between the growth conditions and essential oil composition of Hyptis suaveolens from Alfenas (MG), Brazil. The plants were grown in a greenhouse, four treatments were used and they were harvested at two different periods of time (60 and 135-day-old plants). The essential oil composition was determined by GC-MS analysis. The terpenes spathulenol, globulol, dehydroabietol, a-cadinol and beta-phellandrene were the major constituents found in the essential oil. Oxygenated sesquiterpenes represented the main group of constituents in most of the treatments. The major changes in the essential oil composition were found in 135-day-old plants grown under NPK deficiency. We also identified three groups of volatile components that have not been previously described in H suaveolens.

Neste trabalho foi avaliado o teor de extrativos em madeiras de eucalipto, por meio de extrações com acetona, mistura de tolueno:etanol (2:1), clorofórmio e diclorometano. As maiores porcentagens de extrativos totais foram obtidas ao utilizar acetona como solvente. Os extratos obtidos em acetona e tolueno:etanol foram ressuspendidos em diclorometano, para avaliação do teor de extrativos lipofílicos. As porcentagens desses extrativos foram semelhantes às obtidas com diclorometano ou clorofórmio, em extrações diretas. Os extratos foram analisados por espectroscopia no infravermelho, para identificação dos principais grupos funcionais dos constituintes extraídos.

The extractives content in eucalypt woods were evaluated using direct extractions with acetone, mixture of toluene:ethanol (2:1), chloroform and dichloromethane. The largest percentages of extractives were obtained using acetone as solvent. The extracts obtained in acetone and toluene:ethanol were dissolved in dichloromethane to establish the percentage of lipophilic extractives. The percentages of these extractives were similar to those obtained with dichloromethane or chloroform by direct extractions. The extracts were analyzed by infrared spectroscopy to identify the main functional groups.

Ensaios comportamentais foram conduzidos com indivíduos de colônias monogínicas e poligínicas de Acromyrmex subterraneus molestans a fim de avaliar a habilidade discriminatória de suas operárias. Estes bioensaios mostraram que esta subespécie não é capaz de discriminar entre não companheiras e companheiras de ninho. Entretanto, companheiras de mesma colônia discriminam operárias pertencentes à outra subespécie, Ac. subterraneus subterraneus. Nesta situação, não houve diferença na resposta de operárias oriundas de colônias monogínicas e poligínicas. Similaridades ou diferenças no perfil químico de ambas as subespécies podem explicar a ausência ou presença de agressividade entre operárias. O perfil químico de colônias de mesma subespécie foi muito similar entre si e muito distinto entre subespécies. O número de rainhas não influenciou a composição química cuticular das operárias e nem o seu comportamento discriminatório.

Behavioral assays were conducted with individuals from monogynous and polygynous colonies of Acromyrmex subterraneus molestans to evaluate the discriminatory ability of ant workers. These bioassays showed that this subspecies could not discriminate among non-nestmates or nestmate workers. However, nestmates of these same colonies did discriminate among workers of another subspecies Ac. subterraneus subterraneus. When discrimation occurred there were no differences in the response of workers from either monogynous or polygynous colonies. Similarities or differences in the chemical profile of both subspecies explained the absence or occurence of aggressiveness among workers. The chemical profile of colonies of the same subspecies was very similar among them, although distinct among subspecies. The number of queens did not influence the cuticular chemical composition of the workers or their behavior.

In this paper we report the synthesis of biologically active compounds through a [3+4] cycloaddition reaction to produce the main frame structure, followed by several conventional transformations. The 1,2alpha,4alpha,5-tetramethyl-8-oxabicyclo[3.2.1]oct-6-en-3-one (11) obtained from a [3+4] cycloaddition reaction was converted into 1,2alpha,4alpha,5-tetramethyl-6,7-exo-isopropylidenedioxi-8 -oxabicyclo[3.2.1]octan-3-one (13) in 46% yield. This was further converted into the alcohols 1,2alpha,4alpha,5-tetramethyl-6,7-exo-isopropylidenedioxi-8-oxabicyclo[3.2.1]octan-3 alpha-ol (14), 1,2alpha,4alpha,5-tetramethyl-6,7-exo-isopropylidenedioxi-8 -oxabicyclo[3.2.1]octan-3beta-ol (15), 1,2alpha,4alpha,5-tetramethyl-3-butyl-6,7-exo-isopropylidenedioxi-8-oxabicyclo[3.2.1]octan-3 alpha-ol (17), 1,2alpha,4alpha,5-tetramethyl-3-hexyl-6,7-exo-isopropylidenedioxi-8-oxabicyclo[3.2.1]octan-3 alpha-ol (18) and 1,2alpha,4alpha,5-tetramethyl-3-decyl-6,7-exo-isopropylidenedioxi-8-oxabicyclo[3.2.1]octan-3 alpha-ol (19). Dehydration of 17, 18 and 19 with thionyl chloride in pyridine resulted in the alkenes 20, 21 and 22 in ca. 82% - 89% yields from starting alcohols. The herbicidal activity of the compounds synthesized was evaluated at a concentration of 100 µg g-1. The most active compound was 21 causing 42,7% inhibition against Cucumis sativus L.

This study aimed to analyse the content and the composition of the essential oil of five accesses of mentrasto (Ageratum conyzoides). Five accesses of mentrasto with three repetitions were used. The accesses were obtained in Mariana-MG (AMA), Piranga-MG (API), Visconde do Rio Branco (ARB) and Viçosa-MG (AVB and AVP). The essential oil was obtained by hydrodistillation and the identification of the oil components by CG and GC/MS. The ARB access presented the higher essential oil content, that is 0.70% (P < 0.05). Eleven chemical compounds were identified. The precocene I was the main constituent in the access API, and the precocene II was the main constituent in the accesses AMA, ARB, AVB and AVP.

Several compounds related to helminthosporic acid (3) were synthesized via the [3+4] cycloaddition. The reaction of 3-hydroxymethyl-2-methylfuran (12) with 1,1,3,3-tetrabromo-4-methylpentan-2-one (13) resulted in 7-hydroxymethyl-4alpha-isopropyl-1alpha-methyl-8-oxabicyclo[3.2.1]oct-6-en-3-one (8) (37%) and 7-hydroxymethyl-2alpha-isopropyl-1alpha-methyl-8-oxabicyclo[3.2.1]oct-6-en-3-one (14) (12%), which were converted into 7-formyl-4alpha-isopropyl-1alpha-methyl-8-oxabicyclo[3.2.1]oct-6-en-3-one (16) (32% from 8) and 7-formyl-2alpha-isopropyl-1alpha-methyl-8-oxabicyclo[3.2.1]oct-6-en-3-one (18) (40% from 14), respectively. Reduction of (8) resulted in 7-hydroxymethyl-4alpha-isopropyl-1alpha-methyl-8-oxabicyclo[3.2.1]oct-6 -en-3alpha-ol (11) (63% from 8) and 7-hydroxymethyl-4alpha-isopropyl-1alpha-methyl-8-oxabicyclo[3.2.1]oct-6-en-3 beta-ol (15) (30% from 8). The 4alpha-isopropyl-1alpha-methyl-3-oxo-8-oxabicyclo[3.2.1]oct-6-en-7-oic acid (19) was obtained by oxidation of (16) (78%). The results of biological tests are described in details. The best result was observed for compound (15) that caused 76% inhibition on the root growth of D. tortuosum.

Phytochemical investigation of the aerial parts and roots of Mucuna cinerea led to the isolation of a mixture of fatty acids, triacylglicerols, beta-sitosterol, stigmasterol, stigmasterol glucoside, daucosterol, asperglaucide (4) and the isoflavonoids prunetin (1), genistein (2), medicarpin (3), daidzein (5), 7-O-alpha-glycopiranosyl daidzein (6). An in vitro bioassay was carried out with compounds 1-4, at the concentration of 50 and 5 mug mL-1 against the phytonematodes M. incognita and H. glycines. Although the four compounds showed some nematocidal property, the most active was (1), causing 70% mortality of M. incognita at the concentration of 50 mug mL-1.

The alkene 2,4-dimethyl-8-oxabicyclo[3.2.1]-oct-6-en-3-one (3) was converted to 1,3,10-trimethyl-8-oxabicyclo[5.3.0]-dec-3-ene-2,9-dione (7) and 1,3-dimethyl-8-oxabicyclo[5.3.0]-dec-3-ene-2,9-dione (8) with a 55% overall yield in both cases. Lactones (7) and (8) were converted in two steps to 1,3,4-trimethyl-13-methylene-6-oxatricyclo[8.3.0.0(3,7)]-trideca-2,5,12-trione (12) (63%) and 1,3-dimethyl-13-methylene-6-oxatricycle[8.3.0.0(3,7)]-trideca-2,5,12-trione (13) (45% from 8). The effect of lactones (7), (8), (12), (13) and the intermediates (5) and (6), at the concentration of 250 mug mL-1, on the growth of Cucumis sativus L. and Sorghum bicolor L. was evaluated. The best results were observed for lactone (13) that caused 100% inhibition on the root growth of C. sativus and lactone (12) that inhibited 90% of the root growth for S. bicolor.