Crescimento dos frutos de laranjeira 'Salustiana' situados em ramos anelados com diversas relações de folhas/frutos

A relação entre a área foliar e o crescimento dos frutos é um tema que freqüentemente recebe a atenção dos pesquisadores, por influenciar diretamente na produtividade das plantas e na qualidade dos frutos. Neste trabalho, avaliou-se o efeito da área foliar sobre o crescimento dos frutos da laranjeira 'Salustiana'. Foram utilizados ramos com 12 meses de idade e com apenas um fruto terminal. Os ramos foram anelados visando a manter diversas relações de folhas/fruto. Avaliaram-se, semanalmente, o crescimento dos frutos e os teores de amido presentes nas folhas durante um período de 42 dias. O crescimento dos frutos, avaliado na "fase de crescimento II", dependeu da área foliar disponível por fruto, sendo que 30 folhas foram suficientes para garantir o seu crescimento. As reservas de amido nas folhas dependeram da área foliar disponível por fruto e reduziram à medida que os frutos apresentaram aumentos no diâmetro e nas massas fresca e seca.The relationship between the foliar area and the fruit growth is an important theme because affects the tree productivity and fruits quality. In this work was evaluated the effect of the foliar area on the growth of the Salustiana's sweet orange fruits. Girdled shoots of 12 months were used with a single terminal fruit and several leaves-fruit ratios. It was evaluated, weekly, the fruit growth and the leaves starch contents during 42 days. The fruit growth, evaluated in the stage II, depended on the available leaf area per fruit, provided that 30 leaves were enough to guarantee its growth. The starch reserves in the leaves depended on the available leaf area per fruit and they reduced with the increase in the diameter and dry and fresh weight of the fruits

Efecto del glifosato sobre el crecimiento y acumulación de azúcares libres en dos biotipos de lolium perenne de distinta sensibilidad al herbicida

El movimiento sistémico del glifosato está determinado por el transporte de fotoasimilados. A su vez, la capacidad de un destino de consumir los asimilados está condicionada por su actividad metabólica. Pese a su importancia, la relación entre el glifosato y la síntesis de azúcares en hojas fuente ha sido poco abordada. El objetivo del presente trabajo fue evaluar los efectos del glifosato sobre el crecimiento y la acumulación de azúcares libres en dos biotipos de Lolium perenne de baja y alta sensibilidad al herbicida. Se trabajó con clones de ambos tipos de plantas, en macollaje, tratados con 1.440 g e.a. ha-1 de glifosato y sin tratamiento herbicida como controles. Se evaluó periódicamente el efecto del glifosato sobre el rebrote de hojas hasta las 50 horas post-aplicación y sobre los niveles de azúcares libres totales, reductores y no reductores en hojas a 1, 2, 3 y 5 días post-aplicación. A partir de las 25 horas post-aplicación, el glifosato provocó una disminución del crecimiento del 58% en el biotipo susceptible, con una acumulación de azúcares libres superior al 90% con relación al control, desde el primer día post-aplicación en adelante. La inhibición del crecimiento, inducida por el glifosato en plantas susceptibles, no depende de la limitación del traslado de fotoasimilados desde la parte aérea. Por tanto, la acumulación de azúcares libres en hojas podría explicarse por la caída en la tasa de crecimiento. En el biotipo de baja sensibilidad, en el que no se detectó inhibición del crecimiento, estos efectos fueron limitados.The systemic movement of glyphosate is determined by the transport of photoassimilates. In turn, the capacity of a destination to consume assimilates is conditioned by their metabolic activity. Despite its importance, the relationship between the glyphosate and the sugar synthesis from source leaves has been little studied. The aim of this work was to determine the effect of glyphosate on the growth and free sugar accumulation of two Lolium perenne biotypes of low and high glyphosate sensitivity. It was worked with clones of both types, in tillering, sprayed with 1,440 g a.e. ha-1 of glyphosate as treatments and without herbicide as controls. The glyphosate effects on the regrowth of leaves was studied until 50 hours post-application and on total free sugar, reducing free sugar and nonreducing free sugar from leaves to 1, 2, 3 and 5 days post-application were periodically evaluated. From 25 hours after glyphosate application, it caused on the susceptible biotype a growth decrease of 58% and an accumulation of free sugar above 90% compared to controls. In susceptible biotypes, growth inhibition does not depend on a reduced photoassimilate translocation from the overground part. Therefore, the free sugar accumulation in leaves could be explained by the fall in the rate of growth. These effects are limited in the low sensitivity biotype, where growth inhibition has not been detected

Tomato Fruit Chromoplasts Behave as Respiratory Bioenergetic Organelles during Ripening

During tomato (Solanum lycopersicum) fruit ripening, chloroplasts differentiate into photosynthetically inactive chromoplasts. It was recently reported that tomato chromoplasts can synthesize ATP through a respiratory process called chromorespiration. Here we show that chromoplast oxygen consumption is stimulated by the electron donors NADH and NADPH and is sensitive to octyl gallate (Ogal), a plastidial terminal oxidase inhibitor. The ATP synthesis rate of isolated chromoplasts was dependent on the supply of NAD(P)H and was fully inhibited by Ogal. It was also inhibited by the proton uncoupler carbonylcyanide m-chlorophenylhydrazone, suggesting the involvement of a chemiosmotic gradient. In addition, ATP synthesis was sensitive to 2,5-dibromo-3-methyl-6-isopropyl-p-benzoquinone, a cytochrome b(6)f complex inhibitor. The possible participation of this complex in chromorespiration was supported by the detection of one of its components (cytochrome f) in chromoplasts using immunoblot and immunocytochemical techniques. The observed increased expression of cytochrome c(6) during ripening suggests that it could act as electron acceptor of the cytochrome b(6)f complex in chromorespiration. The effects of Ogal on respiration and ATP levels were also studied in tissue samples. Oxygen uptake of mature green fruit and leaf tissues was not affected by Ogal, but was inhibited increasingly in fruit pericarp throughout ripening (up to 26% in red fruit). Similarly, Ogal caused a significant decrease in ATP content of red fruit pericarp. The number of energized mitochondria, as determined by confocal microscopy, strongly decreased in fruit tissue during ripening. Therefore, the contribution of chromoplasts to total fruit respiration appears to increase in late ripening stages