Battle in the New World: \u3ci\u3eHelicoverpa armigera\u3c/i\u3e versus \u3ci\u3eHelicoverpa zea\u3c/i\u3e (Lepidoptera: Noctuidae)

The corn earworm Helicoverpa zea (Boddie) and the old world bollworm Helicoverpa armigera (HuÈbner) (Lepidoptera: Noctuidae) are allopatric species and occur in important agricultural crops. In maize, both species tend to infest the ear. The introduction of H. armigera in Brazil has created a new scenario, where these Helicoverpa species might cohabit and interact with one another, affecting the prevalence of each species in the agroecosystem, integrated pest management, and insect resistance management. In this study, larval occurrence and proportion of these species in maize was assessed in three regions of Brazil during three crop seasons. Interaction between the species was evaluated in interspecific and intraspecific scenarios under laboratory and field conditions. Helicoverpa zea was predominant in Rio Grande do Sul and the Planaltina, DF (central Brazil). In western Bahia, H. zea was predominant in the first collection, but approximately equal in number to H armigera in the second crop season. Both species exhibit high cannibalism/predation rates, and larval size was the primary factor for larval survival in the interaction studies. Larva of H. zea had higher survival when interacting with H. armigera, indicating that H. zea has an advantage in intraguild interactions with H. armigera in maize. Overall, the results from this study indicate that maize might play a role as a source of infestation or a sink of insecticide or Bt protein unselected H. armigera populations, depending on the H. zea:H. armigera intraguild competition and adult movement in the landscape

N′-[(2E)-3-Phenyl­prop-2-eno­yl]benzo­hydrazide

In the title compound, C16H14N2O2, the conformation about the C=C bond is E, and the two amide groups are effectively orthogonal [the C—N—N—C torsion angle is 104.5 (2)°]. In the crystal structure, the amide groups groups associate via N–H⋯O hydrogen bonding, forming supra­molecular tapes with undulating topology along the c-axis direction

Crystal structures and Hirshfeld surface analyses of (E)-N′-benzylidene-2-oxo-2H-chromene-3-carbohydrazide and the disordered hemi-DMSO solvate of (E)-2-oxo-N′-(3,4,5-trimethoxybenzylidene)-2H-chromene-3-carbohydrazide: lattice energy and intermolecular interaction energy calculations for the former

The crystal structures of the disordered hemi-DMSO solvate of (E)-2-oxo-N'-(3,4,5-tri-meth-oxy-benzyl-idene)-2H-chromene-3-carbohydrazide, C20H18N2O6·0.5C2H6OS, and (E)-N'-benzyl-idene-2-oxo-2H-chromene-3-carbohydrazide, C17H12N2O3 (4: R = C6H5), are discussed. The non-hydrogen atoms in compound [4: R = (3,4,5-MeO)3C6H2)] exhibit a distinct curvature, while those in compound, (4: R = C6H5), are essential coplanar. In (4: R = C6H5), C-H⋯O and π-π intra-molecular inter-actions combine to form a three-dimensional array. A three-dimensional array is also found for the hemi-DMSO solvate of [4: R = (3,4,5-MeO)3C6H2], in which the mol-ecules of coumarin are linked by C-H⋯O and C-H⋯π inter-actions, and form tubes into which the DMSO mol-ecules are cocooned. Hirshfeld surface analyses of both compounds are reported, as are the lattice energy and inter-molecular inter-action energy calculations of compound (4: R = C6H5).info:eu-repo/semantics/publishedVersio

External marking and behavior of early instar \u3ci\u3eHelicoverpa armigera\u3c/i\u3e (Lepidoptera: Noctuidae) on soybean

Helicoverpa armigera Hübner (Lepidoptera: Noctuidae) is a pest of major agricultural crops, such as soybean and cotton. A better understanding of larval movement is important for its integrated management and resistance management. Studies with neonates through second instar larvae are still limited by the difficulties involving the handling and observation of these instars. Many studies require marking larvae, and most research involving marking is focused on moths. However, our study investigated aspects of larval behavior of the second instar of H. armigera on soybean plants. The dyes luminous powder red and Sudan Red 7B were tested as external larval markers. Both dyes successfully marked the larvae for most of 1 stadium (48 h) without deleterious effects, and are useful for short-period behavioral studies. Luminous powder red was selected for the H. armigera larval behavior study on soybean because of ease of detection during both day and night. Second instar on-plant movement was consistent, independent of the d period (morning, afternoon, evening). In general, larvae established their feeding site within a few hours of release, and remained feeding on soybean leaves. Second instar behavior suggests that management by nocturnal insecticide application, based on H. armigera larval movement, would not have an advantage over daytime application. Helicoverpa armigera Hübner (Lepidoptera: Noctuidae) está entre as principais pragas de importancia para culturas agrícolas, como soja e algodão. Compreender o comportamento larval desta espécie, principalmente durante os estádios iniciais é de suma importância para seu manejo integrado e para o manejo de populações resistentes. No entanto, pesquisas com neonatas ou lagartas de segundo ínstar são limitadas devido às dificuldades envolvendo o manuseio e observação de insetos tão diminutos. Muitos desses estudos requerem a marcação de indivíduos, e até o momento, a maioria das pesquisas com marcação de insetos é focada em adultos. Assim, nosso estudo investigou aspectos do comportamento de lagartas de segundo instar de H. armigera em plantas de soja. Estudos prévios também foram realizados com o intuito de se avaliar métodos alternativos e eficazes para marcação de estádios iniciais das larvas desse noctuídeo e suas aplicações em estudos de comportamento. Para tanto, os corantes luminous powder (azul e vermelho) e Sudan (azul e vermelho 7B) foram testados por meio da incorporação em dieta artifical e polvilhamento sobre as lagartas. Baseado em nossos ensaios prévios de laboratório, os corantes incorporados na dieta artifical apresentaram efeitos variáveis sobre os parâmetros biológicos de H. armigera e baixa persistência após o segundo ínstar. Os corantes aplicados por polvilhamento marcaram com sucesso as lagartas e luminous powder vermelho foi selecionado para o estudo de comportamento de lagartas de segundo ínstar em plantas de soja. Lagartas de segundo ínstar apresentaram comportamento de movimento nas plantas semelhantes, independentemente do período de avaliação (manhã, tarde e noite). Em geral, a maioria das lagartas estabeleceram seu sítio de alimentação após algumas horas e permaneceram se alimentando sobre as folhas de soja. Os resultados de comportamento de larvas de H. armigera em segundo instar, documentado no presente trabalho, indicam que aplicacões noturnas de insecticidas não representa vantagem para aumento da eficiência de controle, quando comparado com aplicacões de inseticidas durante o dia

5-(3-Nitro­benz­yl)-1,3,4-thia­diazol-2-amine

In the title mol­ecule, C9H8N4O2S, the dihedral angle between the thia­diazole and benzene rings is 73.92 (8)° and the thia­diazole group S atom is orientated towards the benzene ring, the central S—C—C—C torsion angle being 45.44 (18)°. In the crystal, supra­molecular tapes mediated by N—H⋯N hydrogen bonds and comprising alternating eight-membered {⋯HNCN}2 and 10-membered {⋯HNH⋯NN}2 synthons are formed along [010]. The tapes are consolidated into a three-dimensional network by a combination of C—H⋯O, C—H⋯S and C—H⋯π inter­action

(2E)-N′-[(E)-4-Chloro­benzyl­idene]-3-phenyl­prop-2-enohydrazide monohydrate

The conformation about each of the imine and ethene bonds in the title hydrazide hydrate, C16H13ClN2O·H2O, is E. The hydrazide mol­ecule is approximately planar (r.m.s. deviation of the 20 non-H atoms = 0.172 Å). The most significant twist occurs about the ethene bond [C—C=C—C = 164.1 (5)°] and the dihedral angle formed between the benzene rings is 5.3 (2)°]. In the crystal, the presence of N—H⋯Ow and O—H⋯Oc (× 2; w = water and c = carbon­yl) hydrogen bonds leads to a supra­molecular array in the bc plane

Variação sazonal da composição do óleo essencial de Myrcia salzmannii Berg. (Myrtaceae)

This work report the seasonal variation of composition of the volatile oils from leaves and from flowers of Myrcia salzmannii harvested in the sand dunes of Salvador, Bahia, northeastern region of Brazil in the years 2001 and 2003. The oils were analyzed by GC-FID and GC-MS being identified 49 components. Nine essential oil samples of leaves collected on different months and years and one sample of flowers were analyzed. β-Caryophyllene and α-humulene were the only compounds present in all of the samples being the first the majority compound

(2E)-N′-Benzoyl-3-(4-nitro­phen­yl)prop-2-enohydrazide

In the title compound, C16H13N3O4, the dihedral angle between the terminal benzene rings is 14.02 (7)°. The carbonyl groups are anti with respect to each other, which facilitates their participation in the formation of supra­molecular chains. Each side of the –C(=O)N(H)N(H)C(=O)– residue associates with a centrosymmetrically related mol­ecule, resulting in the formation of essentially flat ten-membered {⋯O=CNN(H)}2 synthons. The resultant chains are further consolidated in the crystal structure via C—H⋯O contacts

Enzymatic inhibition studies of selected flavonoids and chemosystematic significance of polymethoxylated flavonoids and quinoline alkaloids in Neoraputia (Rutaceae)

Our taxonomic interest in the Neoraputia stimulated an investigation of N. paraensis searching for alkaloids. Fractions were monitored by ¹H NMR and ESI-MS/MS and only those which showed features of anthranilate alkaloids and flavonoids absent in the previous investigations were examined. Stems afforded the alkaloids flindersine, skimmianine, 8-methoxyflindersine and dictamnine; leaves yielded 3',4',7,8-tetramethoxy-5,6-(2,2-dimethylpyrano)-flavone, 3',4',5,7,8-pentamethoxyflavone, 5-hydroxy-3',4',6,7-tetramethoxyflavone, 3',4'-methylenedioxy-5,6,7-trimethoxyflavone and 5-hydroxy-3',4'-methylenedioxy-6,7-dimethoxyflavone. The alkaloids have remained undiscovered for 10 years. A number of flavonoids isolated from N. paraensis, N. magnifica, Murraya paniculata, Citrus sinensis graft (Rutaceae), Lonchocarpus montanus (Leguminosae) were evaluated for their ability to inhibit the enzymatic activity of the protein glyceraldehyde-3-phosphate dehydrogenase from Trypanosoma cruzi. Highly oxygenated flavones and isoflavone were the most actives.Nosso interesse quimiotaxonômico sobre Neoraputia nos estimulou a examinar N. paraensis, visando a busca de alcalóides. As frações foram monitoradas via RMN ¹H e ESI-EM/EM e foram analisadas somente aquelas cujos espectros apresentavam características de alcalóides do ácido antranílico e flavonóides não isolados anteriormente. Foram isolados do caule os alcalóides flindersina, skimmianina, 8-metoxiflindersina e dictamnina; das folhas os flavonóides 3',4',7,8-tetrametoxi-5,6-(2,2-dimetilpirano)-flavona, 3',4',5,7,8-pentametoxiflavona, 5-hidroxi-3',4',6,7-tetrametoxiflavona, 3',4'-metilenodioxi-5,6,7-trimetoxiflavona e 5-hidroxi-3',4'-metilenodioxi-6,7-dimetoxiflavona,. Os alcalóides do ácido antranílico não foram encontrados em dez anos. Vários flavonóides isolados de N. paraensis, N. magnifica, Murraya paniculata, enxerto de Citrus sinensis (Rutaceae) e Lonchocarpus montanus (Leguminosae) foram testados frente a gliceraldeído-3-fosfato desidrogenase de Trypanosoma cruzi, visando verificar seus potenciais em inibir a atividade da enzima. Os flavonóides polimetoxilados e um isoflavonóide foram os mais ativos.380387Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES