43 resultados para Kelly, Howard A. (Howard Atwood), 1858-1943


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In 1961, field investigations on "sºva de vidro" (parasol ant, Atta laevigata (Fred. Smith, 1858) were carried out at Piracicaba and other regions of the State of São Paulo (Brazil). This species was found to be a serious pest of cultivated plants, specially Eucalyptus and cotton. The ant makes its colony in any kind of soil, but it prefers to live in the poor ones.

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Em experimentos conduzidos em casa-de-veget§Ã£o e em canteiros, toletes de cana-de-§Ãºcar foram armazenados por tempo e em condições variáveis, em seguida inoculados com cultura pura de Ceratocystis paradoxo, e plantados. Os resultados mostraram que: 1) - o armazenamento pode aumentar o índice de germin§Ã£o, na dependência da variedade de cana, e da época do ano; 2) - nas condições do presente trabalho, o armazenamento em ambiente úmido mostrou-se tão bom ou melhor que o em ambiente sêco; 3) - o armazenamento aumenta a suscetibilidade da cana a C. paradoxa; 4) - o armazenamento diminui o nível de auxina em algumas, variedades, manifestado através da redução da curvatura do colmo, quando plantado inteiro.

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A description is given of a female sand fly (Diptera: Psychodidae - Phlebotominae) similar to Brunptomyia spinosipes (Floch & Abonnenc, 1943).

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The assessment of yellow fever vaccine thermostability both in lyophilized form and after reconstitution were analyzed. Two commercial yellow fever vaccines were assayed for their thermal stability. Vaccines were exposed to test temperatures in the range of 8 (graus) C to 45 (graus) C. Residual infectivity was measured by a plaque assay using Vero cells. The titre values were used in an accelerated degradation test that follows the Arrhenius equation and the minimum immunizing dose was assumed to be 10 (ao cubo) particles forming unit (pfu)/dose. Some of the most relevant results include that (i) regular culture medium show the same degradation pattern of a reconstituted 17D-204 vaccine; (ii) reconstituted YF-17D-204 showed a predictable half life of more than six days if kept at 0 (graus) C; (iii) there are differences in thermostability between different products that are probably due to both presence of stabilizers in the preparation and the modernization in the vaccine production; (iv) it is important to establish a proper correlation between the mouse infectivity test and the plaque assay since the last appears to be more simple, economical, and practical for small laboratories to assess the potency of the vaccine, and (v) the accelerated degradation test appears to be the best procedure to quantify the thermostability of biological products.