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1.
Sci Total Environ ; 808: 152158, 2022 Feb 20.
Article in English | MEDLINE | ID: mdl-34871680

ABSTRACT

Agricultural productivity cannot be sustained without the application of plant protection measures. Within the framework of integrated pest management (IPM), the use of chemical pesticides should be limited to the last option among the available practices. Even though their use remains common, it carries associated environmental and human health risks. One of the most accepted practices within IPM is the reduction of spraying events and/or pesticide applied doses. DOSA3D is a decision support system that allows the dose to be adjusted to the specific treatment scenario. For this, DOSA3D calculates the optimal application volume rate by estimating the leaf area index and takes into account the overall spraying efficiency and the pest or disease to be controlled. The system adopts specific minimum volume rates for fruit trees and vineyards without compromising the crop health status. To establish the adjusted dose, the labeled or the adviser prescription concentration is kept. Resulting adjusted doses provided by DOSA3D achieved pesticide savings up to 53% in fruit trees and 60% in vineyards. DOSA3D has been validated against the main diseases and pests of fruit trees and vineyards: brown spot and psylla in pear orchards; alternaria blotch disease, apple scab, codling moth, oriental moth and red spider mite in apple orchards; powdery mildew, brown rot, aphids, thrips and mites in peach orchards; and, powdery mildew, yellow spider mite and leafhoppers in grapevine orchards. In addition, a methodology called Green Way is presented to provide consistent and crop safety pesticide doses when these are labeled as concentration or ground area doses.


Subject(s)
Malus , Pesticides , Agriculture , Animals , Farms , Fruit , Humans
2.
Langmuir ; 20(18): 7703-10, 2004 Aug 31.
Article in English | MEDLINE | ID: mdl-15323522

ABSTRACT

The oligothiophene derivative 4-(5' " '-decyl-[2,2';5',2' ';5' ',2' ";5' ",2' " '] pentathiophen-5-yl)-butyric acid (D5TBA) was synthesized by Stille cross-coupling methods using functionalized thiophene monomers. The structural and mechanical properties of D5TBA self-assembled monolayers on mica have been studied by atomic force microscopy (AFM). The self-assembled films were prepared by immersing the mica in dilute chloroform or tetrahydrofuran (THF) solutions. The films were predominantly of monolayer thickness with molecules packed in nearly upright orientations. In regions covered with multilayers, the molecules in each monolayer were oriented opposite to those in the neighboring ones, that is, with COOH-COOH and CH3-CH3 contact. The nature of the end group in contact with the substrate depended on the solvent used and the degree of hydration of the substrate, with hydrophobic chloroform solvent favoring the methyl end down and hydrophilic THF favoring the acid group end down. The orientation could also be controlled by dipping using the Langmuir-Blodgett technique.

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