Multiplicação in vitro DE Ficus carica L.: efeito da cinetina e do ácido giberélico

A cultura da figueira é afetada pelo vírus-do-mosaico e a cultura de tecidos é uma alternativa para se proceder à limpeza clonal. Neste trabalho, objetivou-se estudar o efeito da cinetina e GA3 na multiplicação in vitro da figueira. Segmentos nodais foram inoculados em meio de cultura WPM contendo as seguintes combinações de cinetina (0; 0,5; 1; 2 e 4 mg.L-1) e GA3 (0, 2, 4, 6 e 8 mg.L-1). Avaliaram-se número e comprimento dos brotos, peso da matéria fresca e seca da parte aérea, número de raízes, peso da matéria fresca e seca do sistema radicular e de calos. A utilização de 0,5 mg.L-1 de cinetina promoveu melhor taxa de multiplicação in vitro de Ficus carica. O GA3 reduziu a formação e multiplicação dos brotos e induziu ao estiolamento, à hiperidricidade, clorose e necrose apical das plântulas.

Desenvolvimento de mudas de bromélia (Neoregelia cruenta (R. Graham) L. B. Smith) cultivadas em diferentes substartos e adubação foliar

As bromélias apresentam formas exóticas com uma grande diversidade de cores e de flores, constituindo importantes espécies para uso em paisagismo e floricultura. em conseqüência disto, são muito comercializadas. Porém, parte das plantas que se encontram no mercado, ainda são provenientes do extrativismo. Esta situação é também reflexo do pequeno número de informações sobre técnicas de propagação e cultivo. Uma das limitações é o desconhecimento do tipo de substrato e adubação adequados ao cultivo destas espécies. Assim, o objetivo deste trabalho foi avaliar o crescimento de bromélias do Neoregelia cruenta, cultivadas em diferentes substratos e adubações foliares através da altura, do número de folhas, da matéria fresca e seca, da parte aérea e das raízes. As mudas utilizadas foram provenientes de cultura de tecidos. Após um período de pré-aclimatização, foram transplantadas para estufa sem nebulização. Os substratos foram constituídos da mistura de diferentes proporções de solo, areia, casca de arroz carbonizada e por um substrato comercial à base de vermiculita. Aos substratos foi aplicada adubação foliar, combinando uréia e sacarose, em intervalos de quinze dias. Os resultados obtidos mostraram que as interações entre os substratos, dose de sacarose e de uréia, não afetaram a altura das mudas e o número de folhas. O uso de sacarose também não influenciou o desenvolvimento das mudas. O substrato comercial à base de vermiculita, independente da aplicação de adubação foliar, proporcionou maior altura das mudas e número de folhas. A aplicação de uréia apresentou efeito linear crescente durante o período avaliado.

Influência do substrato e do tipo de fertilizante na aclimatação de mudas de bananeira 'Prata-Anã'

Objetivando-se avaliar a influência do substrato e tipo de fertilizante na aclimatação de mudas de bananeira 'Prata-Anã', provenientes de micropropagação, foi instalado um experimento em blocos casualizados, no esquema fatorial 5 x 3, com quatro repetições. Os substratos utilizados foram: S1 - Terra de subsolo + casca de arroz carbonizada + substrato comercial Rendimax Floreira®; S2 - Terra de subsolo + casca de arroz carbonizada + composto orgânico Organifol®; S3 - Terra de subsolo + casca de arroz carbonizada + composto orgânico Organifol® 9% SiO; S4 - substrato comercial Technes Vivatto®; S5 - Areia grossa + casca de arroz carbonizada + Rendimax Floreira®, todos na proporção 1:1:1 (v/v/v). Os fertilizantes utilizados foram: SF - sem fertilizante; FLL - fertilizante de liberação lenta, 14-14-14 (5,0 kg m-3) misturado ao substrato; e FLN - fertilizante de liberação normal, 14-14-14 (5,0 kg m-3) aplicado em cobertura, 30 dias após o plantio. As mudas foram plantadas em sacos de polietileno quando apresentavam quatro a cinco folhas, sendo mantidas em viveiro com 50% de sombreamento. Foram feitas medidas de altura, diâmetro do colo e número de folhas, e determinada a massa seca das mudas. As diferenças químicas das misturas utilizadas como substrato, juntamente com o tipo de fertilizante utilizado, proporcionaram crescimento diferenciado das mudas. O substrato S4 pode ser utilizado sem fertilização. Os substratos S2 e S3 devem ser utilizados com fertilizante de liberação normal ou lenta de nutrientes, e S1 e S5, sendo pobres em nutrientes, com fertilizante de liberação lenta.

Production of yacon plantlet (Polymnia sonchifolia poep. et endl.) in different organic fertilization

The work was carried out in nursery of the Agronomical Science College (ASC) UNESP-Botucatu, in period from September 21(st) to October 31(st) 2000. The propagation material (rhizophores) was obtained from plants, which were cultivated in the area of ASC. The rhizophores were selected according to their vigor and size. Healthy rhizophores were chosen between 15 and 25 g, which were treated with benomil (0,6%, 10 minutes). As a basic commercial substratum Solomix((R)) was used with mixing cattle manure and chicken manure in the following proportions: T1- pure substratum; T2 - substratum + cattle manure (1:1), T3- substratum + cattle manure (2:1); T4- substratum + chicken manure (4:1). The yacon rhizophores presented good shoots in all substrata with exception of T4. For all parameters no significant difference between the pure commercial substratum and its mixture with cattle manure were observed; however, the addition the chicken manure in the studied proportions revealed harmful effect on the survival and development of the plantlets. The results indicated, that the viability of smaller size rhizophores was higher as the size conventionally used in Brazil (60 to 80 g).

In vitro conservation and low cost micropropagation of Cochlospermum regium (Mart. Ex. Scharank)

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Pejibaye palm (Bactris gasipaes) propagative structures and seedlings morphological study

Palm of Arecoideae subfamily, the pejibaye palm occurs mostly at Tropical America areas, and has achieved outstanding economic importance for heart-of-palm production with traditional farming. This work aimed to describe and record propagation structures and seedlings, throughout the different stages of their germination process, since this species is mainly propagated by seeds. The seeds were set for germination on trays with cotton and sterilized water. Representative samples were taken out from each of the different germination stages. They were photographed and drafted using a clear chamber. The propagation structures and seeds external surface were outlined and photographed. The seeds were longitudinally cut for observation and documentation of the inner morphology. The first germinative event was the growth of an undifferentiated, approximately globular cells mass, which emerged from the micropilar depression. Then, the cells mass acquired a cylinder aspect, with the early shoot and root differentiation taking place. Later, there was evidence of primary root and aerial portion. This shoot was coated by a closed and chlorophylled sheath. A lateral root outgrown at the primary root's base and an adventitious root became visible at the embryonic axis. Three other sheaths evolved at the shoot, unrolling one at a time, allowing, finally, the emergence of the primary leaf which is bifid and has parallel veins, typical of its family. Internally, an haustorial structure was developed and seemed to be related with the digestion of the endosperm, occupying, gradually, all the seed's internal space.

Vegetative propagation of Mikania glomerata: Micro-propagation and cuttings

The scope of this work was to compare two systems for vegetative propagation: conventional one (from cut stems) and in vitro micropropagation from axillary buds. Nodal segments (1 cm) of Mikania glomerata were used as explants. The experiments were evaluated in relation to number of shoots; % of rooting; number of roots and total fresh weight. Multiple shoots developed in MS containing 0.5 mg/L BAP. Rooting was induced in the presence of 1.0 mg/L IBA. Stems with five buds and one pair of leaves were the most appropriate for the production of cuttings. The time necessary for developing a protocol for the production of M. glomerata micropropagated plantlets was 6 months, whereas only half time was required to produce plantlets from stem cuttings. The greatest problem met during micropropagation was the culture contamination by endophytic bacteria and fungi.

Micropropagação de Calendula officinalis L

Micropropagation of Calendula officinalis L. is usually propagated through seeds and therefore shows high diversity in flower size and colour, what causes quantitative and qualitative chemical variability. A micropropagation protocol was established for clonal propagation of this species to achieve homogeneous biomass, more appropriate for the production of phytotherapics. Explants harvested from capitula were the most appropriate for the micropropagation process. MS culture medium supplemented with 1.0 mgL-1 BAP and 6.0 gL-1 Phytagel™ enhanced shoot proliferation, while MS medium supplemented with 0.5 mgL-1 Kinetin and 6.0 gL-1 Phytagel™, increased shoot elongation. Plantlets (80%) cultured in MS/2 medium supplemented with 1.0 mgL-1 de IBA rooted.

Enraizamento in vitro e aclimatização de mudas micropropagadas de Aloe vera L.

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

Micropropagação de babosa (Aloe vera L.)

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

Enraizamento de plantas cultivadas in vitro

The adventitious rooting process of in vitro cultured plantlets is a technique that has been employed for the vegetative propagation of a significant number of native and exotic species. Many factors are associated with the rooting stage influencing positive and/or negatively the establishment of micropropagation protocols. The objective of this work was a literature review of the main inherent factors concerning in vitro rooting process including the correlation among others the endogenous and exogenous auxins levels, juvenility, genotype, mineral nutrition, culture medium conditions, addition of growth regulators and other substances as phenolic compounds and active coal besides growth environmental conditions of in vitro cultures. Although the complete elucidation of all processes involved with rooting of in vitro cultured plants has not been achieved so far, a comprehensive study of the main factors that interfere on rooting is fundamental for the establishment of new researches that might contribute for the rooting of economically important plants.

Micropropagação de Salvia officinalis L. com avaliação do teor de fenóis totais e atividade antioxidante

Stem cuts and seeds of Salvia officinalis were incubated on nutrient media for plantlets production and analysis of the total phenolic compounds, total flanovoids and antioxidant activity in micropropagated plants. Explants were obtained from seedlings and inoculated on MS with different concentrations of benzylaminopurine (BAP) and indolbutyric acid (IBA). After 30 and 60 days of incubation, the explants were scored for percentage of contaminated, dead and oxidized explants and mean bud numbers. For bud formation, the most efficient treatment was the medium containing BAP at 1 mg L-1, for the plantlet height the better medium was the control without the addition of plant regulator. IBA promoted the formation of few roots. Our results indicated that stem cuts incubated on media containing BAP and/or IBA did not increase the total flavonoid contents, but increased the total phenolics' by BAP and high antioxidant activity by 1 mg L-1 BAP.

Morfologia de sementes e de estádios iniciais de plântulas de espécies de Bromeliaceae da Amazônia

Seeds of Aechmea bromeliifolia, A. castelnavii (Bromelioideae); Dyckia duckei, D. racemosa (Pitcairnioideae) and Tillandsia adpressiflora (Tillandsioideae) were collected in the Amazon regions (Mato Grosso) and studied to describe morphological characterization and post-seminal development, which can be taxonomically useful, and to assess percent germination. All the species have epigeous germination and produce cryptocotyledonary plantlets. Seeds have no dormancy and percent germination is high (over 86%), which facilitates the production of seedlings and conservation studies. Exclusive characteristics of the genera include: the seed coat of Aechmea (Bromelioideae) has mucilage that prevents desiccation; whereas that of Dyckia (Pitcairnioideae) has membranaceous wings and that of Tillandsia (Tillandsioideae) has feathery appendages, both of which make dispersal easier and establish the epiphytic habit. Initial post-seminal development of Aechmea (Bromelioideae) and Dyckia (Pitcairnioideae) is marked by the emergence of primary roots, interpreted as a basal character, whereas that of Tillandsia adpressiflora (Tillandsioideae) is marked by the emergence of the cotyledon, interpreted as a derived character. Dyckia and Tillandsia have a small tank only in the seedling phase while the contrary occurs in Aechmea.

Propagação in vitro de Cattleya trianaei (Linden & Reichenbach fil.) (Orchidaceae) em meios de culturas e com doses de fertilizante comercial

The use of culture media produced with commercial fertilizers can represent a simple and low cost alternative for commercial orchid propagation. The aim of this study was to evaluate the in vitro growth of plantlets of Cattleya trianaei in culture medium MS reduced and and formulated with Peters® NPK 10-30-20 in different doses. 90 day-old plantlets with two leaflets were submitted to five treatments (T1 - reduced MS; T2 - Peters® 1 g L -1; T3 - Peters® 2 g L-1; T4 - Peters® 3 g L -1 and T5 - Peters® 5 g L-1) arranged in a completely randomized design with five replicates with 25 plantlets for each treatment and incubated during 180 days, with subcultures at each 60 days, when the number of roots, root length, number of leaves, shoot length and shoot fresh matter were evaluated. The simplified culture medium with fertilizer Peters® 3 g L -1 presented results statistically different as for the number of roots, number of leaves, shoot length and shoot fresh matter and it can be recommended for in vitro growth of this ornamental orchid.

Seleção de agentes alternativos ao ágar para propagação de plântulas de Cattleya loddigesii Lindley (Orchidaceae)

The aim of this study was to evaluate the in vitro growth of Cattleya loddigesii in alternative agents to agar with starch and physical matrix with acclimatization of regenerated plants. Protocorms with 90 days after sowing (0.5 cm of length) were subcultured in 1/2 MS culture medium among the treatments consisting of: agar 7 g L-1 (T1, which corresponds the control), agar 3,5 g L-1 with cassava starch 30 g L-1 (T2), cassava starch 60 g L-1 (T3), cotton fiber (T4) and chopped polyurethane foam (T5). Plantlets were retained in these treatments for over 150 days, and at the end of in vitro culture, were analyzed by their biometric data and acclimatized in a greenhouse during 120 days and evaluated the survival and relative growth rate (RGR). The substrate comprising of chopped polyurethane foam (T5) showed greater efficiency for growth in vitro and also increased survival rate, while substrate cassava starch (T3) provided delay for plantlet growth. Therefore, chopped polyurethane foam is recommended because of low cost and suitable characteristics for the propagation of Cattleya loddigesii.