Methods for overcoming dormancy in Stryphnodendron pulcherrimum seeds.

A impermeabilidade do tegumento das sementes é um fenômeno observado em várias espécies tropicais. Essa condição causa germinação baixa e desuniforme. O presente estudo objetivou identificar métodos para superar a dormência em sementes de Stryphnodendron pulcherrimum. Sementes de quatro matrizes foram submetidas aos seguintes tratamentos: imersão em ácido sulfúrico por 2, 4, 6, 8, 10 e 12 min e escarificação com lixa. As sementes foram semeadas em substrato de areia e serragem (1:1). Avaliou-se os dias para iniciar a emergência de plântulas (DIE), emergência de plântulas (EP), índice de velocidade de emergência (IVE), germinação (G), sementes duras (SD), sementes mortas (SM), sementes dormentes (SDM) plântulas anormais (PA), massa seca da parte aérea (MSPA) e massa seca das raízes (MSR). O delineamento utilizado foi inteiramente casualisado com quatro repetições de 25 sementes por tratamento. Os dados foram submetidos à análise de variância e as médias comparadas pelo teste de Tukey (p < 0,05). Diferenças significativas entre tratamentos foram observadas para IVE, EP, G, SD, MSPA e MSR. Maior porcentagem de SD foi observada nas sementes não escarificadas (85%). Maior porcentagem de germinação foi observada nas sementes escarificadas em ácido sulfúrico por 10 min (82%) e 12 min (74%). Esses tratamentos também mostraram maiores IVE, MSPA e MSR, indicando serem os mais eficientes para superar a dormência.

Identification of dormancy-associated MADS-box genes in apple.

2011

Germinação de Ternstroemia brasiliensis Cambess. (Pentaphylacaceae) de floresta de restinga

The main purpose of this work was to study the germination of Ternstroemia brasiliensis seeds both in laboratory and field conditions in order to contribute to understanding the regeneration ecology of the species. The seeds were dispersed with relatively high moisture content and exhibit a recalcitrant storage behaviour because of their sensitivity to dehydration and to dry storage. The germinability is relatively high and is not affected either by light or aril presence. The absence of the dormancy and the low sensitivity to far red light can enable to seeds to promptly germinate under Restinga forest canopy, not forming a soil seed bank. The constant temperatures of 25 ºC and 30 ºC were considered optimum for germination of T. brasiliensis seeds. Temperature germination parameters can be affected by light conditions. The thermal-time model can be a suitable tool for investigating the temperature dependence on the seed germination of T. brasiliensis. The germination characteristics de T. brasiliensis are typical of non pioneer species, and help to explain the distribution of the species. Germination of T. brasiliensis seeds in Restinga environment may be not limited by light and temperature; otherwise the soil moisture content can affect the seed germination.

Estudo da aptidão fisica e fatores de risco para doenças cronicas não-transmissiveis em trabalhadores da limpeza urbana da cidade de Goiania

Universidade Estadual de Campinas . Faculdade de Educação Física

Convergence of developmental mutants into a single tomato model system: 'Micro-Tom' as an effective toolkit for plant development research

Background: The tomato (Solanum lycopersicum L.) plant is both an economically important food crop and an ideal dicot model to investigate various physiological phenomena not possible in Arabidopsis thaliana. Due to the great diversity of tomato cultivars used by the research community, it is often difficult to reliably compare phenotypes. The lack of tomato developmental mutants in a single genetic background prevents the stacking of mutations to facilitate analysis of double and multiple mutants, often required for elucidating developmental pathways. Results: We took advantage of the small size and rapid life cycle of the tomato cultivar Micro-Tom (MT) to create near-isogenic lines (NILs) by introgressing a suite of hormonal and photomorphogenetic mutations (altered sensitivity or endogenous levels of auxin, ethylene, abscisic acid, gibberellin, brassinosteroid, and light response) into this genetic background. To demonstrate the usefulness of this collection, we compared developmental traits between the produced NILs. All expected mutant phenotypes were expressed in the NILs. We also created NILs harboring the wild type alleles for dwarf, self-pruning and uniform fruit, which are mutations characteristic of MT. This amplified both the applications of the mutant collection presented here and of MT as a genetic model system. Conclusions: The community resource presented here is a useful toolkit for plant research, particularly for future studies in plant development, which will require the simultaneous observation of the effect of various hormones, signaling pathways and crosstalk.

Preservation of Phakopsora pachyrhizi uredospores

This study compared different temperatures and dormancy-reversion procedures for preservation of Phakopsora pachyrhizi uredospores. The storage temperatures tested were room temperature, 5 degrees C, -20 degrees C and -80 degrees C. Dehydrated and non-dehydrated uredospores were used, and evaluations for germination (%) and infectivity (no. of lesions/cm(2)) were made with fresh harvested spores and after 15, 29 76, 154 and 231 days of storage. The dormancy-reversion procedures evaluated were thermal shock (40 degrees C/5 min) followed or not by hydration (moist chamber,24 h). Uredospores stored at room temperature were viable only up to a month of storage, regardless of their hydration condition. Survival of uredospores increased with storage at lower temperatures. Dehydration of uredospores prior to storage increased their viability, mainly for uredospores stored at 5 degrees C, -20 degrees C and -80 degrees C. At 5 degrees C and -20 degrees C, dehydrated uredospores showed increases in viability of at least 47 and 127 days, respectively, compared to non-dehydrated spores. Uredospore germination and infectivity after storage for 231 days (7.7 months), could only be observed at -80 degrees C, for both hydration conditions. At this storage temperature, dehydrated and non-dehydrated uredospores exhibited 56 and 28% of germination at the end of the experiment, respectively. Storage at -80 degrees C also maintained uredospore infectivity, based upon levels of Infection frequency, for both hydration conditions. Among the dormancy-reversion treatments applied to spores stored at -80 degrees C, those involving hydration allowed recoveries of 85 to 92% of the initial germination.