Atividade residual de herbicidas pré-emergentes aplicados na cultura da soja sobre o milheto cultivado em sucessão

O objetivo deste estudo foi avaliar a atividade residual de herbicidas utilizados no manejo de plantas daninhas em pré-emergência da cultura da soja, bem como verificar seus efeitos sobre o milheto cultivado em sucessão. Utilizaram-se parcelas de 80 m², em delineamento de blocos casualizados, com quatro repetições, em esquema de parcelas subdivididas 5 x 4, correspondendo à aplicação dos herbicidas imazaquin (0,160 kg ha-1), diclosulam (0,035 kg ha-1), sulfentrazone (0,600 kg ha-1) e flumioxazin (0,050 kg ha-1) e uma testemunha, aplicados logo após a semeadura do cultivar de soja Msoy-6101. Nas subparcelas, realizou-se a semeadura do milheto, cultivar ADR-7010, em quatro períodos, correspondendo a 0, 40, 80 e 120 dias após a aplicação dos herbicidas (DAA). Durante a condução do ensaio, foram determinados os níveis de intoxicação, estande, altura e massa seca da parte aérea das plantas de milheto. No final do ciclo foi avaliado o rendimento de grãos da cultura. O híbrido de milheto ADR-7010 apresentou elevada sensibilidade com relação à atividade residual dos herbicidas sulfentrazone, diclosulam e imazaquin quando cultivado logo após a aplicação destes. A bioatividade dos herbicidas imazaquin, diclosulam e flumioxazin não foi suficiente para alterar o rendimento de grãos do milheto cultivado em sucessão à soja (120 DAA), mostrando que esse intervalo de tempo é suficiente para dissipação desses herbicidas. Dos herbicidas pré-emergentes avaliados, o sulfentrazone apresentou maior atividade residual, influenciado negativamente o rendimento da cultura durante o intervalo de tempo estudado.

Atividade residual de herbicidas aplicados em pós-emergência na cultura da soja sobre o milheto cultivado em sucessão

O objetivo deste trabalho foi avaliar a atividade residual de herbicidas utilizados em pós-emergência da cultura da soja sobre o milheto cultivado em sucessão. O experimento foi realizado em Latossolo Vermelho distroférrico de textura argilosa em região de cerrado. Os herbicidas chlorimuron-ethyl (0,015 kg ha-1), imazethapyr (0,060 kg ha-1), imazethapyr (0,100 kg ha-1) e fomesafen (0,250 kg ha-1) foram utilizados em pós-emergência do cultivar de soja Msoy-6101. Utilizou-se o delineamento de blocos casualizados, com quatro repetições, em esquema de parcelas subdivididas (5 x 4). Nas subparcelas, realizou-se a semeadura do milheto (híbrido ADR-7010) em quatro períodos, correspondendo a 0, 40, 80 e 120 dias após a aplicação dos herbicidas (DAA). Durante a condução do ensaio, avaliou-se a intoxicação da cultura aos 7 e 28 dias após a emergência, o estande, a altura e a matéria seca da parte aérea das plantas de milheto. Ao final do ciclo da cultura, determinou-se o rendimento de grãos. O imazethapyr (0,060 kg ha-1) e chlorimuron-ethyl (0,015 kg ha-1) não alteraram significativamente o rendimento da cultura do milheto em semeaduras posteriores a 80 DAA. Para fomesafen, o intervalo mínimo de segurança entre a aplicação e a semeadura do milheto foi de 100 dias. Por outro lado, maior persistência foi observada para imazethapyr na dose 0,100 kg ha-1, chegando a 120 dias de bioatividade sobre o milheto, que teve seu rendimento de grãos alterando mesmo quando semeado durante esse período.

Crescimento de espécies bioindicadoras do residual do herbicida (imazethapyr+imazapic), semeadas em rotação com arroz Clearfield®

Neste trabalho, determinou-se o efeito residual do herbicida Only® (imazethapyr+imazapic) sobre plantas de milho, pepino, rabanete e tomate, semeadas em solo no qual o herbicida foi aplicado há 1.100 dias. O estudo foi realizado em casa de vegetação, com o delineamento experimental de casualização por bloco, com quatro repetições por tratamento. Os tratamentos avaliados foram o residual do herbicida Only® aplicado sob as plantas de arroz CL na safra 2006/2007, nas doses de 0, 100, 150 e 200 g ha-1 do produto comercial, acrescido de 0,5% do adjuvante Dash®. Foram semeadas sob as parcelas 15 sementes de cada espécie bioindicadora (milho, pepino, rabanete e tomate), sendo estas desbastadas para 10 plantas após a germinação. Após 60 dias da data da semeadura, foram avaliadas a altura de plantas, a massa seca da parte aérea e a massa seca das raízes, sendo esta última não realizada nas plantas de milho e de pepino. Os dados obtidos foram submetidos à análise da variância (p<0,05) e testados por modelos de regressão polinomial. Conclui-se que houve presença de atividade residual da mistura comercial dos herbicidas (imazethapyr+imazapic) do grupo das imidazolinonas em solo após 1.100 dias da aplicação dos herbicidas. Isso indica que as plantas de milho, pepino, rabanete e tomate podem ser utilizadas como espécies bioindicadoras de atividade residual da mistura comercial dos herbicidas (imazethapyr+imazapic) e que o rabanete e o tomate são mais sensíveis à presença do produto, quando comparados ao milho e ao pepino.

Lixiviação de saflufenacil e residual após períodos de seca

O objetivo deste trabalho foi avaliar a lixiviação de saflufenacil em Latossolo Vermelho-Amarelo (textura média, pH 5,6) e Latossolo Vermelho distrófico (textura argilosa, pH 5,2 e pH 6,0), assim como os efeitos de períodos de seca no residual desse herbicida. A lixiviação de saflufenacil (0,10 g i.a ha-1) e, adicionalmente, a lixiviação de diuron + hexazinone (1.170 + 330 g i.a. ha-1) foram avaliadas sob simulação de chuva (40 mm). O herbicida saflufenacil aplicado em solo argiloso com pH 6,0 apresentou lixiviação até a profundidade de 25 cm, porém ela foi mais pronunciada na faixa de 15 a 20 cm. Quando o herbicida foi aplicado no mesmo solo, mas com pH 5,2, houve lixiviação até a profundidade de 15 cm. Em solo de textura média, a lixiviação foi elevada até a profundidade de 25 cm. Para diuron+hexazinone, no solo argiloso, independentemente do pH, houve lixiviação até 25 cm de profundidade. Todavia, em solo de textura média a lixiviação ocorreu até 40 cm de profundidade. Em relação ao efeito residual do saflufenacil após períodos de seca (0, 15, 30, 45, 60 e 90 dias) em um Latossolo Vermelho distrófico (textura argilosa), foi verificado efeito fitotóxico no bioindicador maior ou igual a 80% até os 28 dias de seca.

Atividade residual de diuron, oxyfluorfen e prometryne no controle de Euphorbia heterophylla

As aplicações de herbicidas em pré-emergência têm por finalidade a obtenção da atividade residual no início do ciclo das culturas. Assim, o objetivo deste trabalho foi avaliar a atividade residual dos herbicidas diuron, oxyfluorfen e prometryne, aplicados isoladamente ou em misturas, no controle de Euphorbia heterophylla. Oito experimentos foram conduzidos em casa de vegetação, aplicando-se doses dos herbicidas ou das misturas aos 30, 20, 10 e 0 dias antes da semeadura da planta daninha (DAS). Com o diuron e prometryne, foram observados controles satisfatórios até 20 DAS nas doses a partir de 1,07 e 1,6 kg ha-1, respectivamente. Quanto ao oxyfluorfen, foi registrado um período residual inferior, obtendo-se controle mínimo de 80% até 10 DAS nas doses a partir de 0,324 kg ha-1. Em relação às misturas dos herbicidas, a mistura diuron+prometryne promoveu controle superior a 85% por períodos de até 30 dias, quando aplicada na menor dose (1+2 kg ha-1), e de 20 dias, quando aplicada na dose de 2+1 kg ha-1. Visando obter esse mesmo patamar de controle por 30 dias, foi necessário 1+0,288 kg ha-1 da mistura diuron+oxyfluorfen. A mistura prometryne+oxyfluorfen apresentou um mínimo de 80% de controle no período de 10 dias, quando utilizada a dose de 1+0,192 kg ha-1.

Residual herbicides in weed management for glyphosate-resistant soybean in Brazil

In agricultural production systems where the glyphosate-resistant soybean crop (Glycine max) is grown and the practice of crop rotation with alternative herbicides is not adopted, the exclusive and continuous use of glyphosate has led to the occurrence of resistant weed populations that may limit or compromise the benefits of this technology. Thus, the efficacy of weed management programs, including the use of residual herbicides (sulfentrazone, flumioxazin, imazethapyr, diclosulan, chlorimuron and s-metolachlor) applied in preemergence and followed by in-crop postemergence applications of glyphosate (PRE-POST) were compared to glyphosate postemergence only programs - POST. The study was conducted across nine locations during the 2009/2010 and 2010/2011 growing seasons. PRE-POST programs were efficient in the control of Amaranthus viridis, Brachiaria plantaginea, Bidens pilosa, Commelina benghalensis, Eleusine indica, Euphorbia heterophylla and Raphanus raphanistrum, with the level of control being similar when comparing the program with two applications of glyphosate POST. Some PRE-POST programs were not efficient in controlling Cenchrus echinatus, Ipomoea hederifolia and Ipomoea triloba. Sulfentrazone and diclosulam PRE-POST programs improved the control of Ipomoea triloba compared to sequential applications of glyphosate alone. No significant differences in soybean yield were observed between any of the herbicide treatments or study locations. The use of residual herbicides in preemergence followed by glyphosate in-crop postemergence provides consistent weed control and reducing early season weed competition. Furthermore, these programs utilize at least two herbicide modes of action for herbicide use diversity, which will be needed to stay ahead of resistance build-up, regardless of when weeds may appear.

Eficiência e residual no solo de herbicidas na cultura do feijão

Avaliou-se a eficiência de herbicidas na cultura do feijão e a possível ação residual desses produtos sobre as culturas de sorgo e de milho cultivadas em sucessão. O experimento foi realizado em campo e em casa de vegetação, avaliando-se os seguintes tratamentos: fomesafen (250 g L-1) e a mistura comercial de bentazon e imazamox (600 g L‑1 + 28 g L-1) nas doses de 25, 50, 75 e 100% da dose recomendada dos respectivos produtos comerciais, bem como a mistura em tanque desses herbicidas nas proporções de 75 + 25, 50 + 50 e 25 + 0,75%, além de duas testemunhas: uma capinada e outra sem capina. O fomesafen na dose de 250 g ha-1 proporcionou boa produtividade de feijão, porém prejudicou o crescimento de plantas de sorgo nas amostras de solo coletadas até 183 dias após a aplicação (DAA), indicando grande persistência do herbicida. No solo coletado aos 153 DAA, observou-se intoxicação nas plantas de milho, mas não houve influência no acúmulo de matéria seca da parte aérea nem na produção de grãos. A mistura pronta de bentazon e imazamox não foi eficiente no controle de plantas daninhas até a colheita do feijão. Contudo, quando a essa mistura adicionou-se o fomesafen, houve redução da dose do fomesafen em 75%, com ótimo controle de plantas daninhas e fácil condição de colheita do feijão, além de menor risco de carryover em plantas de sorgo e de milho. A persistência do fomesafen no solo não foi alterada com a mistura em tanque de bentazon e imazamox.

Effect of trolox C on cardiac contracture induced by hydrogen peroxide

Hydrogen peroxide (H2O2) perfused into the aorta of the isolated rat heart induces a positive inotropic effect, with cardiac arrhythmia such as extrasystolic potentiation or cardiac contractures, depending on the dose. The last effect is similar to the "stone heart" observed in reperfusion injury and may be ascribed to lipoperoxidation (LPO) of the membrane lipids, to protein damage, to reduction of the ATP level, to enzymatic alterations and to cardioactive compounds liberated by LPO. These effects may result in calcium overload of the cardiac fibers and contracture ("stone heart"). Hearts from male Wistar rats (300-350 g) were perfused at 31oC with Tyrode, 0.2 mM trolox C, 256 mM H2O2 or trolox C + H2O2. Cardiac contractures (baseline elevation of the myograms obtained) were observed when hearts were perfused with H2O2 (Tyrode: 5.9 ± 3.2; H2O2: 60.5 ± 13.9% of the initial value); perfusion with H2O2 increased the LPO of rat heart homogenates measured by chemiluminescence (Tyrode: 3,199 ± 259; H2O2: 5,304 ± 133 cps mg protein-1 60 min-1), oxygen uptake (Tyrode: 0.44 ± 0.1; H2O2: 3.2 ± 0.8 nmol min-1 mg protein-1) and malonaldehyde (TBARS) formation (Tyrode: 0.12 ± 0; H2O2: 0.37 ± 0.1 nmol/ml). Previous perfusion with 0.2 mM trolox C reduced the LPO (chemiluminescence: 4,098 ± 531), oxygen uptake (0.51 ± 0) and TBARS (0.13 ± 0) but did not prevent the H2O2-induced contractures (33.3 ± 16%). ATP (Tyrode: 2.84 ± 0; H2O2: 0.57 ± 0) and glycogen levels (Tyrode: 0.46 ± 0; H2O2: 0.26 ± 0) were reduced by H2O2. Trolox did not prevent these effects (ATP: 0.84 ± 0 and glycogen: 0.27 ± 0). Trolox C is known to be more effective than a -tocopherol or g -tocopherol in reducing LPO though it lacks the phytol portion of vitamin E to be fixed to the cell membranes. Trolox C, unlike vitamin A, did not prevent the glycogen reduction induced by H2O2. Trolox C induced a positive chronotropic effect that resulted in higher energy consumption. The reduction of energy level seemed to be more important than LPO in the mechanism of H2O2-induced contracture

Residual ß-cell function and microvascular complications in type 1 diabetic patients

To determine the influence of residual ß-cell function on retinopathy and microalbuminuria we measured basal C-peptide in 50 type 1 diabetic outpatients aged 24.96 ± 7.14 years, with a duration of diabetes of 9.1 ± 6.2 years. Forty-three patients (86%) with low C-peptide (<0.74 ng/ml) had longer duration of diabetes than 7 patients (14%) with high C-peptide (³0.74 ng/ml) (9 (2-34) vs 3 (1-10) years, P = 0.01) and a tendency to high glycated hemoglobin (HBA1) (8.8 (6-17.9) vs 7.7 (6.9-8.7)%, P = 0.08). Nine patients (18%) had microalbuminuria (two out of three overnight urine samples with an albumin excretion rate (AER) ³20 and <200 µg/min) and 13 (26%) had background retinopathy. No association was found between low C-peptide, microalbuminuria and retinopathy and no difference in basal C-peptide was observed between microalbuminuric and normoalbuminuric patients (0.4 ± 0.5 vs 0.19 ± 0.22 ng/ml, P = 0.61) and between patients with or without retinopathy (0.4 ± 0.6 vs 0.2 ± 0.3 ng/ml, P = 0.43). Multiple regression analysis showed that duration of diabetes (r = 0.30, r2 = 0.09, P = 0.031) followed by HBA1 (r = 0.41, r2 = 0.17, P = 0.01) influenced basal C-peptide, and this duration of diabetes was the only variable affecting AER (r = 0.40, r2 = 0.16, P = 0.004). In our sample of type 1 diabetic patients residual ß-cell function was not associated with microalbuminuria or retinopathy.

Reaction of diphenyl diselenide with hydrogen peroxide and inhibition of delta-aminolevulinate dehydratase from rat liver and cucumber leaves

The interaction of the product of H2O2 and (PhSe)2 with delta-aminolevulinate dehydratase (delta-ALA-D) from mammals and plants was investigated. (PhSe)2 inhibited rat hepatic delta-ALA-D with an IC50 of 10 µM but not the enzyme from cucumber leaves. The reaction of (PhSe)2 with H2O2 for 1 h increased the inhibitory potency of the original compound and the IC50 for animal delta-ALA-D inhibition was decreased from 10 to 2 µM. delta-ALA-D from cucumber leaves was also inhibited by the products of reaction of (PhSe)2 with H2O2 with an IC50 of 4 µM. The major product of reaction of (PhSe)2 with H2O2 was identified as seleninic acid and produced an intermediate with a lambdamax at 265 nm after reaction with t-BuSH. These results suggest that the interaction of (PhSe)2 with mammal delta-ALA-D requires the presence of cysteinyl residues in close proximity. Two cysteine residues in spatial proximity have been recently described for the mammalian enzyme. Analysis of the primary structure of plant delta-ALA-D did not reveal an analogous site. In contrast to (PhSe)2, seleninic acid, as a result of the higher electrophilic nature of its selenium atom, may react with additional cysteinyl residue(s) in mammalian delta-ALA-D and also with cysteinyl residues from cucumber leaves located at a site distinct from that found at the B and A sites in mammals. Although the interaction of organochalcogens with H2O2 may have some antioxidant properties, the formation of seleninic acid as a product of this reaction may increase the toxicity of organic chalcogens such as (PhSe)2.

Cytotoxicity of chlorhexidine digluconate to murine macrophages and its effect on hydrogen peroxide and nitric oxide induction

Chlorhexidine, even at low concentrations, is toxic for a variety of eukaryotic cells; however, its effects on host immune cells are not well known. We evaluated in vitro chlorhexidine-induced cytotoxicity and its effects on reactive oxygen/nitrogen intermediate induction by murine peritoneal macrophages. Thioglycollate-induced cells were obtained from Swiss mice by peritoneal lavage with 5 ml of 10 mM phosphate-buffered saline, washed twice and resuspended (10(6) cells/ml) in appropriate medium for each test. Cell preparations contained more than 95% macrophages. The cytotoxicity was determined by the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-tetrazolium bromide assay and the presence of hydrogen peroxide (H2O2) and nitric oxide (NO) by the horseradish peroxidase-dependent oxidation of phenol red and Griess reaction, respectively. The midpoint cytotoxicity values for 1- and 24-h exposures were 61.12 ± 2.46 and 21.22 ± 2.44 µg/ml, respectively. Chlorhexidine did not induce synthesis or liberation of reactive oxygen/nitrogen intermediates. When macrophages were treated with various sub-toxic doses for 1 h (1, 5, 10, and 20 µg/ml) and 24 h (0.5, 1, and 5 µg/ml) and stimulated with 200 nM phorbol myristate acetate (PMA) solution, the H2O2 production was not altered; however, the NO production induced by 10 µg/ml lipopolysaccharide (LPS) solution varied from 14.47 ± 1.46 to 22.35 ± 1.94 µmol/l and 13.50 ± 1.42 to 20.44 ± 1.40 µmol/l (N = 5). The results showed that chlorhexidine has no immunostimulating activity and sub-toxic concentrations did not affect the response of macrophages to the soluble stimulus PMA but can interfere with the receptor-dependent stimulus LPS.

Antioxidant responses of Laeonereis acuta (Polychaeta) after exposure to hydrogen peroxide

The effects of H2O2 were evaluated in the estuarine worm Laeonereis acuta (Polychaeta, Nereididae) collected at the Patos Lagoon estuary (Southern Brazil) and maintained in the laboratory under controlled salinity (10 psu diluted seawater) and temperature (20°C). The worms were exposed to H2O2 (10 and 50 µM) for 4, 7, and 10 days and the following variables were determined: oxygen consumption, catalase (CAT) and glutathione peroxidase activity in both the supernatant and pellet fractions of whole body homogenates. The concentrations of non-protein sulfhydryl and lipid peroxides (LPO) were also measured. The oxygen consumption response was biphasic, decreasing after 4 days and increasing after 7 and 10 days of exposure to 50 µM H2O2 (P < 0.05). At the same H2O2 concentration, CAT activity was lower (P < 0.05) in the pellet fraction of worms exposed for 10 days compared to control. Non-protein sulfhydryl concentration and glutathione peroxidase activity were not affected by H2O2 exposure. After 10 days, LPO levels were higher (P < 0.05) in worms exposed to 50 µM H2O2 compared to control. The reduction in the antioxidant defense was paralleled by oxidative stress as indicated by higher LPO values (441% compared to control). The reduction of CAT activity in the pellet fraction may be related to protein oxidation. These results, taken together with previous findings, suggest that the worms were not able to cope with this H2O2 concentration.

Hydrogen peroxide induces a specific DNA base change profile in the presence of the iron chelator 2,2’ dipyridyl in Escherichia coli

Pretreatment of Escherichia coli cultures with the iron chelator 2,2’-dipyridyl (1 mM) protects against the lethal effects of low concentrations of hydrogen peroxide (<15 mM). However, at H2O2 concentrations equal to or greater than 15 mM, dipyridyl pretreatment increases lethality and mutagenesis, which is attributed to the formation of different types of DNA lesions. We show here that pretreatment with dipyridyl (1 mM) prior to challenge with high H2O2 concentrations (≥15 mM) induced mainly G:C→A:T transitions (more than 100X with 15 mM and more than 250X with 20 mM over the spontaneous mutagenesis rate) in E. coli. In contrast, high H2O2 concentrations in the absence of dipyridyl preferentially induced A:T→T:A transversions (more than 1800X and more than 300X over spontaneous mutagenesis for 15 and 20 mM, respectively). We also show that in the fpg nth double mutant, the rpoB gene mutation (RifS-RifR) induced by 20 mM H2O2 alone (20X higher) was increased in 20 mM H2O2 and dipyridyl-treated cultures (110X higher), suggesting additional and/or different lesions in cells treated with H2O2 under iron deprivation. It is suggested that, upon iron deprivation, cytosine may be the main damaged base and the origin of the pre-mutagenic lesions induced by H2O2.

Short-term exposure of mice to cigarette smoke and/or residual oil fly ash produces proximal airspace enlargements and airway epithelium remodeling

Chronic obstructive pulmonary disease (COPD) is associated with inflammatory cell reactions, tissue destruction and lung remodeling. Many signaling pathways for these phenomena are still to be identified. We developed a mouse model of COPD to evaluate some pathophysiological mechanisms acting during the initial stage of the disease. Forty-seven 6- to 8-week-old female C57/BL6 mice (approximately 22 g) were exposed for 2 months to cigarette smoke and/or residual oil fly ash (ROFA), a concentrate of air pollution. We measured lung mechanics, airspace enlargement, airway wall thickness, epithelial cell profile, elastic and collagen fiber deposition, and by immunohistochemistry transforming growth factor-β1 (TGF-β1), macrophage elastase (MMP12), neutrophils and macrophages. We observed regional airspace enlargements near terminal bronchioles associated with the exposure to smoke or ROFA. There were also increases in airway resistance and thickening of airway walls in animals exposed to smoke. In the epithelium, we noted a decrease in the ciliated cell area of animals exposed to smoke and an increase in the total cell area associated with exposure to both smoke and ROFA. There was also an increase in the expression of TGF-β1 both in the airways and parenchyma of animals exposed to smoke. However, we could not detect inflammatory cell recruitment, increases in MMP12 or elastic and collagen fiber deposition. After 2 months of exposure to cigarette smoke and/or ROFA, mice developed regional airspace enlargements and airway epithelium remodeling, although no inflammation or increases in fiber deposition were detected. Some of these phenomena may have been mediated by TGF-β1.

Electron paramagnetic resonance study of lipid and protein membrane components of erythrocytes oxidized with hydrogen peroxide

Electron paramagnetic resonance (EPR) spectroscopy of spin labels was used to monitor membrane dynamic changes in erythrocytes subjected to oxidative stress with hydrogen peroxide (H2O2). The lipid spin label, 5-doxyl stearic acid, responded to dramatic reductions in membrane fluidity, which was correlated with increases in the protein content of the membrane. Membrane rigidity, associated with the binding of hemoglobin (Hb) to the erythrocyte membrane, was also indicated by a spin-labeled maleimide, 5-MSL, covalently bound to the sulfhydryl groups of membrane proteins. At 2% hematocrit, these alterations in membrane occurred at very low concentrations of H2O2 (50 µM) after only 5 min of incubation at 37°C in azide phosphate buffer, pH 7.4. Lipid peroxidation, suggested by oxidative hemolysis and malondialdehyde formation, started at 300 µM H2O2 (for incubation of 3 h), which is a concentration about six times higher than those detected with the probes. Ascorbic acid and α-tocopherol protected the membrane against lipoperoxidation, but did not prevent the binding of proteins to the erythrocyte membrane. Moreover, the antioxidant (+)-catechin, which also failed to prevent the cross-linking of cytoskeletal proteins with Hb, was very effective in protecting erythrocyte ghosts from lipid peroxidation induced by the Fenton reaction. This study also showed that EPR spectroscopy can be useful to assess the molecular dynamics of red blood cell membranes in both the lipid and protein domains and examine oxidation processes in a system that is so vulnerable to oxidation.