Factors contributing to genetic differences in low temperature seed germination of tomato (Lycopersicon esculentum Mill.) were examined by comparing the cold germinating (CG) accession PI 341985 the non-cold germinating (NCG) ‘Centennial’ and random F4 lines with varying low temperature germinating abilities. Rate of radicle elongation at 10°C was similar for both parental genotypes indicating that differences in emergence at 10° are not due to growth rates, but rather to more rapid initiation of germination activities in CG. Preincubation of seeds in hypertonic salt solutions enhanced rate of germination at 10°C equally in both lines, but did not substitute for the genetically based cold germinating ability. Low temperature germinating ability is associated with sprouting at high osmotic concentrations, and with a several fold higher rate of increase in peroxidase activity during the first 10 days of incubation at 10°. Germination at 10° of the NCG lines is improved by activated carbon in the germination media whereas no enhancement occurred in CG lines. Inhibition and/or delay in germination at 10° in NCG lines is due, in part, to low temperature induced formation of activated carbon adsorbable inhibitors of seed germination.
Cold tolerance (CT) of 31 tomato accessions (cultivars, breeding lines, and plant introductions) representing six Lycopersicon L. sp. was evaluated during seed germination and vegetative growth. Seed germination was evaluated under temperature regimes of 11 ± 0.5 °C (cold stress) and 20 ± 0.5 °C (control) in petri plates containing 0.8% agar medium and maintained in darkness. Cold tolerance during seed germination was defined as the inverse of the ratio of germination time under cold stress to germination time under control conditions and referred to as germination tolerance index (TIG). Across accessions, TIG ranged from 0.15 to 0.48 indicating the presence of genotypic variation for CT during germination. Vegetative growth was evaluated in growth chambers with 12 h days/12 h nights of 12/5 °C (cold stress) and 25/18 °C (control) with a 12 h photoperiod of 350 mmol.m-2.s-1 (photosynthetic photon flux). Cold tolerance during vegetative growth was defined as the ratio of shoot dry weight (DW) under cold stress (DWS) to shoot DW under control (DWC) conditions and referred to as vegetative growth tolerance index (TIVG). Across accessions, TIVG ranged from 0.12 to 0.39 indicating the presence of genotypic variation for CT during vegetative growth. Cold tolerance during vegetative growth was independent of plant vigor, as judged by the absence of a significant correlation (r = 0.14, P > 0.05) between TIVG and DWC. Furthermore, CT during vegetative growth was independent of CT during seed germination, as judged by the absence of a significant rank correlation (rR = 0.14, P > 0.05) between TIVG and TIG. A few accessions, however, were identified with CT during both seed germination and vegetative growth. Results indicate that for CT breeding in tomato, each stage of plant development may have to be evaluated and selected for separately.
The genetic relationship between cold tolerance (CT) during seed germination and vegetative growth in tomato (Lycopersicon esculentum Mill.) was determined. An F2 population of a cross between accession PI120256 (cold tolerant during both seed germination and vegetative growth) and UCT5 (cold sensitive during both stages) was evaluated for germination under cold stress and the most cold tolerant progeny (the first 5% germinated) were selected. Selected progeny were grown to maturity and self-fertilized to produce F3 families (referred to as the selected F3 population). The selected F3 population was evaluated for CT separately during seed germination and vegetative growth and its performance was compared with that of a nonselected F3 population of the same cross. Results indicated that selection for CT during seed germination significantly improved CT of the progeny during germination; a realized heritability of 0.75 was obtained for CT during seed germination. However, selection for CT during germination did not affect plant CT during vegetative growth; there was no significant difference between the selected and nonselected F3 populations in either absolute CT [defined as shoot fresh weight (FW) under cold stress] or relative CT (defined as shoot FW under cold as a percentage of control). Results indicated that, in PI120256, CT during seed germination was genetically independent of CT during vegetative growth. Thus, to develop tomato cultivars with improved CT during different developmental stages, selection protocols that include all critical stages are necessary.
Seed germination percentage of multiflora rose (Rosa multiflora Thunh.) was much higher under continuous white light than in complete darkness. Red light was the most effective in inducing germination, and far-red light was ineffective. Exposure to red light for 1 min increased germination; this effect was saturated at an exposure of2 min. The red-light effect was reversed by subsequent exposure to far-red light. The results indicate that rose seeds are positively photoblastic, and that the photoreceptor involved is most likely phytochrome.
We compared peach [Prunus persica (L.) Batsch cv. Johnson Elberta] seed germination (G) and seedling emergence (E) after various stratification (St) treatments. Treatments were arranged in factorial combinations of five St durations (20 to 60 days) at eight constant temperatures (0 to 18C) in a completely randomized design followed by repeated measures during forcing time. G and E were recorded every 5 days during forcing. Seed St at 0 to 10C and 0 to 14C promoted G and E, respectively. G and E increased with longer St treatments at promoting temperatures. There was a weak correlation between G and E averaged over the forcing measurements (r 2 = 0.54). The best correlation was between E after 15 days and G after 10 days (r 2 = 0.83). The results indicate that G and E in peach are not identical indicators of endodormancy (ED) release and should not be used interchangeably. Forcing times must be considered when making comparisons between G and E.
This investigation documents the key anatomical features in embryo development of Cypripedium formosanum Hayata, in association with the ability of embryos to germinate in vitro, and examines the effects of culture media and seed pretreatments on seed germination. A better understanding of zygotic embryogenesis for the Cypripedium L. species would provide insights into subsequent germination events and aid in the in vitro propagation of these endangered species. In seeds collected at 60 days after pollination (DAP), soon after fertilization, no germination was recorded. The best overall germination was found at 90 DAP (≈70%), at which time early globular to globular embryos with a single-celled suspensors can be observed. After 135 DAP, the seeds germinated poorly. At this time the inner integument shrinks and forms a tight layer, which encloses the embryo, the so-called “carapace.” Using Nile red stain, a cuticular substance was detected in the carapace, which may play a role in the impermeability of the mature seed and may help the seeds survive in the stringent environment. At maturity (after 210 DAP), the embryo proper has an average size of eight cells along its length and six cells across the width. Lipids and proteins are the main storage products within the embryo. To improve seed germination, experiments were conducted to test the suitability of various media and pretreatments of seeds. When different media were used, except for the Harvais medium at 120 DAP, there was no significant difference in seed germination at three different developmental stages tested. Soaking mature seeds in 1% NaOCl or treating them with ultrasound may slightly increase the germination percentage. For seed germination, our results indicate that the timing of seed collection outweighs the composition of medium and the seed pretreatments.
Two experiments investigated the relationship of light and temperature in seed germination of Fraser fir [Abies fraseri (Pursh) Poir.]. Irradiation during the warm portion of 9/15 hr thermoperiod of 20/10C and 30/20C increased germination percentages after 42 days, and the degree of stimulation depended on the timing of the light exposures. A 1-hr exposure was most effective during the latter part of the warm portion of the thermoperiods, and varying the time of irradiation had the greatest effect at 20/10C. The involvement of phytochrome in this photomorphogenic response was ascertained by demonstration of red/far-red reversibility.
Tomato seeds were more responsive than wheat or lettuce seeds to the presence of an inhibitor in the juice of tomato fruits. Seed germination and seedling growth decreased with increasing concentrations of juice. Inhibition of seed germination in 20% juice with an osmotic concentration of less than 0.1 M was significantly less than in 0.1 M glucose or mannitol with 0.01 M citric acid at pH 4.4. The inhibitor in tomato juice was thermostable, but the effect decreased with prolonged storage at -20°C. There were cultivar differences in the amount of inhibitor present in ripe tomato fruits.
Priming, a controlled-hydration treatment followed by redrying, improves the germination and emergence of seeds from many species. We compared osmotic and matric priming to determine which was the most effective treatment for improving broccoli seed germination and to gain a greater understanding of how seed vigor is enhanced by priming. Broccoli (Brassica oleracea L. var. italica) seeds were osmotically primed in polyethylene glycol (PEG 8000) at -1.1 MPa or matrically primed in a ratio of 1.0 g seed:0.8 g synthetic calcium silicate (Micro-Cel E):1.8 ml water at -1.2 MPa. In the laboratory, germination rates and root lengths were recorded from 5 to 42C and 10 to 35C, respectively. Broccoli seeds germinated poorly at >35C. Root growth after germination was more sensitive to temperatures >30C and <15C than radicle emergence. Matric and osmotic priming increased germination rate in the laboratory, greenhouse, and field. However, matric priming had a greater effect on germination and root growth rates from 15 to 30C. Neither priming treatment affected minimum or maximum germination or root growth temperatures. Both priming treatments decreased the mean thermal time for germination by >35%. The greater germination performance of matrically primed seeds was most likely the result of increased oxygen availability during priming, increased seed Ca content, or improved membrane integrity.
A light requirement for improved seed germination of lowbush blueberry (Vaccinium angustifolium Ait.) was partially overcome by GA treatments; GA at 500, 1000, 2000, and 4000 ppm stimulated early germination of seeds kept in the dark. The germination rate of seeds exposed to an 8 hour light period was also enhanced by GA treatments. Continuous exposure to concentrations above 1000 ppm resulted in abnormally curled seedlings with necrotic root tips.