In vitro multiplication of Swietenia macrophylla King (Meliaceae) from juvenile shoots.

Big-leaf mahogany (Swietenia macrophylla King) is an important species for timber production that is considered the most valuable in the world. For this reason its exploitation is indiscriminate and leads this species to the risk of extinction. Moreover, mahogany is difficult to regenerate naturally and, when used in reforestation programs, plants are severely damaged by the shoot-borer (Hypsipyla grandella Zellar). This work aimed at developing the multiplication stage of micropropagation of Swietenia macrophylla King using juvenile material. After desinfestation, seeds were germinated in MS solid culture medium. Shoot formation from seeds occurred during five months, giving 5.54 nodal segments per seed. These explants were excised, each containing one axillary bud, and transferred on multiplication media. Four experiments with cytokinins were conducted, using media supplemented with 6-benzylaminopurine (BAP) (2.5 to 50.0 ?M), 2- isopentenyladenine (2-iP) (0; 1.1 to 8.8 ?M), combinations of BAP (0; 2.5 to 50.0 ?M) and 2-iP (2.2 ?M). For the first treatments the basal culture medium was MS medium and in the last one MS and QL media were used in separate experiments. When BAP was tested alone, the maximum point of multiplication rate average was obtained on medium containing 23.61 ?M, while 2-iP did not induce bud multiplication. On QL culture medium supplemented with the combinations of BAP (0; 2.5; 5.0; 10.0 e 20.0 ?M ) and 2-iP (2.2 ?M), there was no multiplication. The maximum point of multiplication rate average was 5.7 ?M, obtained when the MS culture medium was supplemented with 18.51 ?M BAP and 2.2 ?M 2-iP

Fitorremediação em solo contaminado pelo metal chumbo.

A fitorremediação é a técnica que faz o uso de plantas para diminuir o nível de contaminação do solo, água e até mesmo do ar. Para este experimento foi utilizado o capim vetiver e o solo originário do Acre, sendo fertilizado, contaminado e separado em 20 vasos. Os experimentos foram feitos em quatro níveis de repetições. O capim foi cultivado na casa de vegetação da Embrapa Solos localizada na Universidade Federal Fluminente (UFF). Foram realizados diversos ensaios nas amostras de solo, na parte aérea do capim e na raiz. O presente trabalho tem por objetivo acompanhar a regressão do metal chumbo nas amostras de solo. O capim vetiver foi eficaz no tratamento de regressão de chumbo

In vitro multiplication of Swietenia macrophylla King (Meliaceae) from juvenile shoots.

Big-leaf mahogany (Swietenia macrophylla King) is an important species for timber production that is considered the most valuable in the world. For this reason its exploitation is indiscriminate and leads this species to the risk of extinction. Moreover, mahogany is difficult to regenerate naturally and, when used in reforestation programs, plants are severely damaged by the shoot-borer (Hypsipyla grandella Zellar). This work aimed at developing the multiplication stage of micropropagation of Swietenia macrophylla King using juvenile material. After desinfestation, seeds were germinated in MS solid culture medium. Shoot formation from seeds occurred during five months, giving 5.54 nodal segments per seed. These explants were excised, each containing one axillary bud, and transferred on multiplication media. Four experiments with cytokinins were conducted, using media supplemented with 6-benzylaminopurine (BAP) (2.5 to 50.0 ?M), 2- isopentenyladenine (2-iP) (0; 1.1 to 8.8 ?M), combinations of BAP (0; 2.5 to 50.0 ?M) and 2-iP (2.2 ?M). For the first treatments the basal culture medium was MS medium and in the last one MS and QL media were used in separate experiments. When BAP was tested alone, the maximum point of multiplication rate average was obtained on medium containing 23.61 ?M, while 2-iP did not induce bud multiplication. On QL culture medium supplemented with the combinations of BAP (0; 2.5; 5.0; 10.0 e 20.0 ?M ) and 2-iP (2.2 ?M), there was no multiplication. The maximum point of multiplication rate average was 5.7 ?M, obtained when the MS culture medium was supplemented with 18.51 ?M BAP and 2.2 ?M 2-iP.200