RESUMO
Sixteen years of archived tufted apple bud moth, Platynota idaeusalis (Walker), trap capture data were compared with archived fruit injury data collected at the Penn State University Fruit Research and Extension Center to define the relationship of trap capture to fruit injury. Pheromone trap capture until 15 June was the best predictor of fruit injury at harvest. Using the regression equation of fruit injury on early season trap capture, and other assumptions about insecticide cost and fruit yield, a management model was developed for apple growers in the Mid-Atlantic region. When the model was tested on archived trap capture and fruit injury data, the results indicated that a grower would lose money on average by always treating and save money on average by never treating. By using the model, a grower could expect to save more money than by never treating. The model showed sensitivity to fruit price, insecticide price, and fruit yield.
Assuntos
Frutas/parasitologia , Controle de Insetos/métodos , Malus/parasitologia , Mariposas/fisiologia , Animais , Tomada de Decisões , Inseticidas , Modelos Biológicos , Feromônios , Análise de Regressão , Estações do Ano , Sensibilidade e EspecificidadeRESUMO
The effect of prohexadione-calcium, a plant growth regulator that inhibits gibberellin metabolism, on Cacopsylla pyricoloa (Foerster) in pear trees, and Choristoneura rosaceana (Harris) and Aphis spireacola Patch, in apple trees was studied. C. pyricoloa and A. spireacola populations were significantly reduced in prohexadione-calcium-treated pear and apple, respectively. Insecticide control of both pests with imidacloprid was synergized in treatments with prohexadione-calcium. In apples treated with prohexadione-calcium, there was a significant reduction in the number of C. rosaceana shelters per tree and amount of fruit injury at harvest attributable to the C. rosaceana. There was an additive effect when tebufenozide was used to control C. rosaceana in trees treated with prohexadione-calcium. Prohexadione-calcium significantly reduced vegetative growth in both pears and apples. Synergistic and additive treatment effects of prohexadione-calcium and pesticides used in this study may be due to better penetration and coverage of pesticides due to reduced foliar growth or to changes in the nutritional quality of the host plants.
Assuntos
Controle de Insetos/métodos , Inseticidas , Ácidos Cetoglutáricos/farmacologia , Malus , Reguladores de Crescimento de Plantas/farmacologia , Pyrus , Animais , Afídeos , Sinergismo Farmacológico , Hemípteros , Lepidópteros , Malus/crescimento & desenvolvimento , Pyrus/crescimento & desenvolvimentoRESUMO
The responses of tufted apple bud moth, Platynota idaeusalis (Walker), the leafroller P. flavedana Clemens, redbanded leafroller, Argyrotaenia velutinana (Walker), and obliquebanded leafroller, Choristoneura rosaceana (Harris), to the pheromone blends of each, as well as to 3 putative generic blends (two- and three-component blends containing pheromone elements of each of the 4 species) were evaluated in small orchard plots. P. idaeusalis and P. flavedana, and A. velutinana and C. rosaceana comprise 2 pairs of species, each pair with broad overlap in pheromone blend, and quite different from one another. Each generic blend suppressed trap captures of all 4 species. The blends for P. idaeusalis and P. flavedana each reduced captures for these species. Furthermore, the blend for P. idaeusalis also suppressed captures of A. velutinana. The P. flavedana blend did not reduce captures of A. velutinana; in fact, at times captures increased. This study determines relative abilities of several sex attractant blends to reduce captures of 4 leafroller species in pheromone traps, presumably reflecting the ability of a blend to reduce orientation of males to females in a large block situation. This is a requisite 1st step in the development of a multispecies mating disruption blend.
Assuntos
Lepidópteros/fisiologia , Malus , Feromônios , Atrativos Sexuais , Animais , Feminino , Masculino , Controle Biológico de VetoresRESUMO
Whether or not surface salt bridges have a strong stabilizing effect on the native structure in proteins remains uncertain. Previous studies of model peptides have shown that salt bridges spaced at i,i +4 along the chain are more stabilizing than those spaced at i,i +3, with a preference for the order acid-base rather than base-acid from N to C terminus. An analysis of the effect of spacing the ion pairs in short helical peptides is presented, in which acidic and basic side chains spaced two or three residues apart alternate along the chain. The mixed spacing proves to be stabilizing relative to pure spacings. A control peptide in which salt bridges were spaced uniformly three residues apart proved to form a beta-sheet structure rather than alpha-helix. This is due to formation of a silk-like apolar face consisting of alanine side chains; the mesoscopic structure formed by these sheets can be imaged by scanning microscopy.
Assuntos
Peptídeos/química , Sais/química , Alanina/química , Sequência de Aminoácidos , Dicroísmo Circular , Microscopia/métodos , Modelos Moleculares , Dados de Sequência Molecular , Peptídeos/síntese química , Conformação Proteica , Tirosina/químicaRESUMO
1. Esterase activity in the tufted apple bud moth was measured spectrophotometrically by the hydrolysis of alpha-naphthyl acetate. 2. Resistant populations from both laboratory and field exhibited significantly greater esterase activity than did the respective susceptible populations. 3. The resistant laboratory population had significantly higher esterase activity than the resistant field population, suggesting that this field population contained a mixture of resistant and susceptible individuals.
Assuntos
Esterases/metabolismo , Mariposas/enzimologia , Animais , Azinfos-Metil , Resistência a Medicamentos/fisiologia , MasculinoRESUMO
The fungicide captan (cis-N-((trichloromethyl)thio) 4-cyclo-hexene-1,2-dicarboximide) was applied at the rate of 2.4 g/l to apple trees (c.v. Golden Delicious) individually or as part of a standard treatment program where it was applied eight times during the growing season together with several pesticides. Leaf samples (100 discs of 2.2 cm diameter) were collected from treated and control trees before treatment and at 0, 1, 3, 7, 14, 28, 56, 90 and 112 days after treatment. Fruit samples were taken at mid-season (56 days) and at harvest (112 days). The objective of this study was to determine the captan residue and mutagenicity of leaf and fruit extracts to ascertain the potential health hazard to agricultural workers in these orchards. Surface residues were extracted from leaves and fruits with methylene chloride. These extracts were subsequently analyzed for captan by gas-liquid chromatography (GLC) utilizing an electron-capture detector, and for mutagenicity with two strains (TA98 and TA100) of Salmonella typhimurium, with and without microsomal enzyme activation. Positive mutagenic effects were observed with strain TA100 at 0-14 days post spray, even with extracts from one leaf disc's surface (3.8 cm2) of the single treatment. Captan residues in these samples indicated a decline from 9.3 micrograms/cm2 at 0 days to 0.80 micrograms/cm2 at 14 days and a trace after 112 days. With the standard treatment, in which captan was incorporated eight times in the program starting at the 7-day interval, leaf extracts showed mutagenic activity at 7, 14, 28 and 90 days. Captan residues at these intervals were 11.4, 5.0, 4.1 and 3.4 micrograms/cm2, respectively. Fruit sample extracts of the standard spray were mutagenic to the tester strains TA100 and TA98 both at mid-season and at harvest. Residues of captan on fruits declined from 10.4 micrograms/cm2 at mid-season to 1.1 micrograms/cm2 at harvest. No mutagenic activity was detected with extracts from fruit samples from the single captan application.
Assuntos
Captana/análise , Frutas/análise , Mutagênicos , Resíduos de Praguicidas/análise , Captana/toxicidade , Contaminação de Alimentos/análise , Testes de Mutagenicidade , Salmonella typhimurium/genéticaRESUMO
Repetitive sequences in intron and spacer DNA could be sites for binding of chromosomal proteins which maintain chromatin structure and control gene activity. Methylation of DNA guides the binding of acidic nonhistone proteins and maintains the differentiation state during DNA replication. Differentiation inducers modify repressor proteins permitting unfolding of chromatin. Histone H 1 must be removed for gene activity. Phosphorylation of nonhistone proteins probably induces allosteric modifications which permit unfolding of chromatin. Acetylation of nucleosomal histones is necessary to permit passage of RNA polymerase. Deacetylation quickly returns the gene to a normal histone repressed state. Chromosomal RNA attached to nonhistone proteins aids the binding of RNA polymerase to the DNA template. Carcinogens can disrupt normal gene control leading to circumvention of normal cell cycle controls.
Assuntos
Cromatina/fisiologia , Regulação da Expressão Gênica , Animais , Diferenciação Celular , Fenômenos Químicos , Química , Proteínas Cromossômicas não Histona/fisiologia , DNA/metabolismo , Histonas/fisiologia , Humanos , Metilação , RNA/fisiologia , Ratos , Sequências Repetitivas de Ácido Nucleico , Transcrição GênicaRESUMO
Circumvention of part of the normal controls of proliferation permits the relatively autonomous proliferation of cells which is characteristic of tumors. Several different mechanisms exist which permit circumvention of proliferation controls. RNA tumor viruses probably induce carcinogenesis by producing a viral kinase which is similar to a cAMP independent tyrosine kinase that is activated by epidermal growth factor. Circumvention of proliferation controls is permitted by modification of gene expression induced by genetic and/or epigenetic mechanisms. There does not appear to be one single mechanism for circumventing proliferation controls present in all tumors. Circumvention of proliferation controls is the basic cause of carcinogenesis.
Assuntos
Neoplasias/etiologia , Diferenciação Celular , Divisão Celular/efeitos dos fármacos , Transformação Celular Neoplásica , Inibição de Contato , Humanos , Neoplasias/fisiopatologia , Proteínas Quinases/metabolismo , Proteínas , Vírus de RNA/enzimologiaRESUMO
Cancer is characterized by a relatively autonomous growth of cells due to a reduced responsiveness to normal controls of proliferation and differentiation. The proliferation of normal cells is regulated at arrest (restriction) points in the cell cycle. Relatively autonomous growth (tumors) can result from various mechanisms which circumvent the normal regulatory controls of the cell cycle.
Assuntos
Ciclo Celular , Divisão Celular , Substâncias de Crescimento/fisiologia , Neoplasias/fisiopatologia , Animais , AMP Cíclico/fisiologia , GMP Cíclico/fisiologia , Fibronectinas/fisiologia , Inibidores do Crescimento/fisiologia , Humanos , Interferons/uso terapêutico , Modelos Biológicos , Neoplasias/tratamento farmacológicoRESUMO
The common element in the induction and progression of tumors by all types of carcinogens may be the random unmasking of embryonic and nonembryonic genes to produce a cell with characteristics that are not well regulated in differentiated tissue and thus exhibit relatively autonomous growth. The neoplastic state is heritable in the same manner as any other differentiated state. Carcinogens act by disrupting the structure of the chromatin DNA-protein-RNA complex and thus changing the differentiation state of the cell. Survival of the neoplactic cells selects for those gene expressions which aid the autonomous neoplastic state. Some mutations may cause alterations that permit unmasking of genes.
Assuntos
Diferenciação Celular , Genes , Modelos Biológicos , Neoplasias/genética , Carcinógenos/farmacologia , Membrana Celular/metabolismo , Transformação Celular Neoplásica , Cromatina/metabolismo , Inibição de Contato , DNA de Neoplasias/metabolismo , DNA Viral/metabolismo , Humanos , Substâncias Intercalantes/metabolismo , MutaçãoRESUMO
The hydrolysis kinetics of 3-quinuclidinyl benzilate were determined over the pH 0-14 range at different temperatures in solutions buffered to a constant pH. Analysis of data extrapolated to zero buffer concentrations permitted construction of an overall rate expression for pH 0-14 and 0-100 degrees. Reaction mechanisms are discussed.