Resumo

Knowledge about the behavior of seeds is important to support studies to minimize the effects of predatory extractivism on ornamental bromeliads. The aim of this study was to evaluate the germination, seed morphology and post-seminal development of Hohenbergia belemii and Neoregelia compacta (Bromeliaceae) in different substrates. Seeds were disinfested with a sodium hypochlorite solution and germinated in four substrates: germitest paper; washed sand; vermiculite; and the commercial substrate Plantmax®. The experimental design was completely randomized in a 2 x 4 factorial scheme, with four repetitions and 50 seeds per repetition. The seeds were sown on the substrates and stored in plastic Gerbox® boxes, which were kept in BOD chambers with 12 hours photoperiod at constant temperature of 30ºC. Data were collected daily to calculate germination percentage and growth performance. The germination started on the 4th day after sowing (DAS) for H. belemii, with stabilization on the 11th DAS, while this occurred from the 5th DAS for N. compacta with stabilization on the 21st DAS. Germination was classified as development of epigeal and cryptocotylar seedlings for both species. The vermiculite substrate had a significant effect on seed germination, GSI (germination speed index) and growth of seedlings of both species. Our findings can support future research on seed technology and also contribute to better knowledge of the evolution of morphological characters of these bromeliad species.(AU)

Resumo

The establishment of minimum growth conditions is essential for in vitro germplasm conservation. Changes to the basic medium and carbon source concentrations are important factors for reducing plant growth in vitro. This study adjusted a protocol for the in vitro conservation of 'Florida Rough' lemon plants. Microcuttings (approximately 1 cm) from plants that were previously cultivated in vitro were inoculated into test tubes with 10 mL of woody plant medium (WPM) at different concentrations (1/1, 1/2 and 1/4) and supplemented with 0, 12.5, 25 and 50 g.L-1 of sucrose, solidified with 7 g.L-1 agar and adjusted to pH 5.8. The experiment was completely randomized in a 3 x 4 factorial design with 15 replications and was maintained under controlled conditions for 360 days. After this period the plant height in cm (PH), the plant dry mass in g (PDM) and the 21 numbers of green leaves (NGL), senescent leaves (NSL) and microcuttings (NM) were evaluated. The variables that best explained the observed behavior of the 'Florida Rough' lemon plants were NGL and PH, with values of 61.63 and 35.08%, respectively. The original concentration of the WPM with the addition of 25 g. L-1 of sucrose yielded the best 'Florida Rough' lemon plant growth reduction in vitro while maintaining the physiologically health of the plants.

O estabelecimento de condições de crescimento mínimo é fundamental para a conservação in vitro de germoplasma. Alterações nas concentrações do meio básico, na fonte de carbono, são fatores importantes na desaceleração do crescimento de plantas in vitro. Este trabalho teve como objetivo ajustar um protocolo de conservação in vitro de plantas do limoeiro 'Rugoso da Flórida'. Microestacas de plantas previamente cultivadas in vitro, com aproximadamente 1 cm, foram inoculadas em tubos de ensaio contendo 10 mL do meio de cultura WPM em diferentes concentrações (1/1, 1/2 e 1/4), suplementado com 0; 12,5; 25 e 50 g.L-1 de sacarose, solidificado com 7 g.L-1 de ágar e o pH ajustado em 5,8. O experimento foi instalado em delineamento inteiramente casualizado com 15 repetições, em esquema fatorial 3 x 4, e mantido sob condições controladas durante 360 dias. Após este período, foram avaliadas altura de planta em cm (AP), número de folhas verdes (NFV), número de folhas senescentes (NFS), número de microestacas (NM) e massa da planta seca em g (MPS). As variáveis que mais contribuíram para explicar a diferença existente no comportamento das plantas do limoeiro 'Rugoso da Flórida' no meio de cultura WPM foram NFV e AP com 61,63 e 35,08%, respectivamente. O meio de cultura WPM na sua concentração original com a adição de 25 g.L-1 de sacarose promoveu os melhores resultados na redução do crescimento das plantas in vitro do limoeiro 'Rugoso da Flórida', mantendo-as fisiologicamente sadias.

Resumo

This study assessed and compared different methods for vegetative propagation of a miniature ornamental pineapple hybrid (ORN-MUT), seeking to determine the best method for production of plantlets, as well as for removal of the PMWaV viral complex from plants cultured in vitro, for production of healthy parent plants. Pineapple wilt is a disease that can cause large economic and is caused by a viral complex called Pineapple mealybug wilt-associated virus (PMWaV). For this, four propagation methods were evaluated (conventional, stem sectioning, micropropagation and etiolation of nodal segments). The time necessary for each method and the number of plants formed were assessed. Stem tips (0.5 mm) were cultured and indexed for three PMWaV types. Conventional propagation produced 17 plantlets per plant in 566 days, stem sectioning produced 2.3 plantlets per stem in 591 days, while the conventional micropropagation technique produced 1,284 plants after four subcultures in 778 days. Stems etiolated for 60 days showed peak production in the second subculture, with 1,224 plants. This method required 883 days to obtain plants with ideal size for transplantation to the field. In turn, stems etiolated for 120 days produced 935 plants at the end of four subcultures, with peak output in the third subculture, in which the plants could be cultivated in the field after 943 days. Conventional micropropagation and etiolation for 60 days were the best methods for production of plantlets of the ORN-MUT hybrid. The results of this work showed that the cultivation of shoot tips is an efficient strategy to remove the PMWaV complex and obtain healthy mother plants and can be a useful tool for other varieties of pineapple.

Resumo

Alcantarea nahoumii(Leme) J. R. Grant is a species native to theAtlantic Forest that stands out for ornamental purposes. The objective of this work was to evaluate the in vitrogerminationof A. nahoumiiseeds and establish a micropropagation protocol for production of seedlings so as to minimize the effects of predatory extractivism and develop an in vitroconservation system. Mature seeds were disinfested, established in three culture media (MS, MS½ and MS⅓) and incubated at four temperatures (20, 25, 30 and 35ºC)in a germination chamber. In the micropropagation experiment, stem segments were introduced in MS medium supplemented with 0.5 μM of 1-naphthaleneacetic acid (NAA) and 0.0, 2.2, 4.4 and 6.6 μM of 6-benzylaminopurine (BAP). For the in vitroconservation, plantlets were established in MS or MS½ medium supplemented with 15 g L-1or 30 g L-1of sucrose. The plants were acclimated with commercial substrate. The highest seed germination percentages were promoted by temperature conditions of 20 and 25ºC, with MS culture medium. The highest multiplication rate of shoots was obtained from the treatment without addition of the growth regulator or when combined with 2.2 μM of BAP + 0.5 μM of NAA. The acclimation of the plants occurred with high survival rate. The species can be conserved in vitrounder slow growth condition for 24 months when incubated in MS medium supplemented with 30 g L-1of sucrose.

Resumo

Plant fiber is a renewable and biodegradable material that can be used effectively to reinforce various composites. Pineapple hybrids selected for their fiber quality are in the phase of agronomic validation in Brazil by the Embrapa Cassava and Fruits research unit. The selection of a hybrid for large-scale fiber production depends on obtaining a large number of seedlings. This study evaluated the morphogenetic response and propagation potential of eight hybrids of Ananas comosus var. erectifolius, for the purpose of producing high-quality seedlings on a large scale. Stem and crown buds were reduced and placed in MS nutritive medium supplemented with BAP at 0.5 mg L-1, NAA at 0.01 mg L-1 and Phytagel® at 2.5 g L-1. After 45 days, the number of oxidized, contaminated and surviving buds was determined. Swollen buds and plantlets were transferred to a multiplication medium containing MS sucrose, salts and vitamins. The propagation potential was evaluated based on the geometric growth rate among sub-cultures. The FIB-NEG hybrid presented the best results for the establishment phase (40.28%). The best propagative potential was obtained from crown buds with the highest values for FIB-EST (3.93), FIB-MIN (3.91) and FIB-BOY (3.91) hybrids.

A fibra vegetal é uma fonte renovável, biodegradável e de excelente desempenho como reforço em compósitos variados. Híbridos selecionados pela qualidade de suas fibras estão em fase de validação agronômica na Embrapa Mandioca e Fruticultura e sua adoção para produção de fibra em larga escala depende de um elevado número de mudas. Este trabalho teve como objetivo avaliar a resposta morfogenética e o potencial propagativo de oito híbridos de Ananas comosus var. erectifolius, com a finalidade de produzir mudas de qualidade em larga escala. Gemas do caule e coroa foram reduzidas, introduzidas em meio nutritivo MS suplementado com BAP a 0,5 mg L-1, ANA a 0,01 mg L-1 e Phytagel® a 2,5 g L-1. Aos 45 dias foram avaliados o número de gemas oxidadas, contaminadas e sobreviventes. Gemas intumescidas e plantas formadas foram transferidas para o meio de multiplicação contendo sacarose, sais e vitaminas MS. Avaliou-se o potencial propagativo a partir de uma taxa de crescimento geométrico entre subcultivos. O híbrido FIB-NEG (40.28%) apresentou os melhores resultados em porcentagem para a fase de estabelecimento. O melhor potencial propagativo foi obtido a partir de gemas de coroa, com os valores mais elevados registrados para os híbridos FIB-EST (3.93), FIB-MIN (3.91) e FIB-BOY (3.91).

Resumo

Genipa americana (jenipapeiro) é uma essência florestal pertencente à família Rubiaceae, que apresenta importância econômica e ambiental, sendo valorizada para produção de alimentos, na recuperação de áreas degradadas, na composição em áreas de preservação permanentes e em sistemas agroflorestais. Objetivou-se avaliar o efeito de diferentes tempos de desidratação em câmara de fluxo laminar e tempos de imersão em solução crioprotetora (MS+0,5M de sacarose) na capacidade regenerativa de ápices caulinares da espécie para estabelecimento de futuros protocolos de criopreservação. Os ápices caulinares foram obtidos de plântulas, acesso Oiteiros, germinadas e cultivadas in vitro. Os explantes foram submetidos ao encapsulamento e a diferentes tempos de imersão em solução crioprotetora e tempos de desidratação em câmara de fluxo laminar. A crioproteção e a desidratação não alteram a viabilidade dos ápices caulinares de jenipapeiro encapsulados ou não encapsulados. A imersão por 24 horas em solução crioprotetora e a desidratação em câmara de fluxo laminar por 2 horas apresentam potencial para uso em futuros trabalhos de criopreservação por encapsulamento-desidratação.

Genipa americana (genipap) is a forest species belonging to the Rubiaceae family that has economic and environmental importance, being valued for food production, recuperation of degraded areas, in the composition in areas of permanent preservation and agroforestry. The objective of this research was to evaluate the effect of different times of dehydration in laminar flow cab and immersion time in cryoprotecting solution (MS+0.5M sucrose) on the regenerative capacity of shoot apices for establishing future cryopreservation protocols. The shoot apices were obtained from seedlings, of Oiteiros accession, germinated and cultured in vitro. Explants were subjected to encapsulation and different exposure times in cryoprotecting solution and dehydration in a laminar flow cab. The cryoprotection and dehydration does not modify the viability of the shoot apices of genipap encapsulated or unencapsulated. Immersion for 24 hours in cryoprotecting solution and the dehydration in a laminar flow cab by 2 hours have potential for use in future studies of cryopreservation by encapsulation-dehydration.