scholarly journals The effect of cytokinins on flax seed germination at low temperature

2011 ◽  
Vol 75 (4) ◽  
pp. 281-284
Author(s):  
Irena Niedźwiedź-Siegień ◽  
Sylwia Bukłaha

Germination of flax seeds (<em>Linum usitatissimum</em> L., cv. Szafir) at 5<sup>o</sup>C was enhanced by continuous white light, gibberellin A3 (GA3), kinetin and benzylaminopurine. GA<sub>3</sub> and kinetin at physiological concentrations (10<sup>-8</sup>-10<sup>-6</sup> M) improved significantly germination in darkness. Stimulatory effect of benzylaminopurine was visible only in the light. Almost no effect of zeatin and isopentenyladenine (2iP) on germination was observed. Possible causes of this differences were suggested.

1973 ◽  
Vol 53 (4) ◽  
pp. 907-910 ◽  
Author(s):  
D. G. DORRELL

In 1971, the percentage of poorly matured flax seeds (Linum usitatissimum L.) in southern Manitoba was unusually high. This seed was discolored and tended to clump due to portions of the capsule septa adhering to the seed coat. Samples of flax seed selected from the new crop survey conducted by the Canadian Grain Commission were divided into normal and poor or weathered seeds. The poor seeds had a lower seed weight, lower percent germination, and darker oil, but an iodine number higher than the normal seeds. There were no consistent differences in oil and protein content. It appears that seeds with this type of weathering are acceptable for crushing but unacceptable for seeding.


2019 ◽  
Vol 13 (3) ◽  
Author(s):  
S. Kraevska ◽  
O. Yeshchenko ◽  
N. Stetsenko

In the world, demand for flax seeds and its processed volumes are increasing. Flax seeds are classified as natural functional food products. This is confirmed by the Ministry of Health of many countries, in particular Canada and the United States of America. Flax germination makes flax seed components biologically available. Each type of plant has its own set of germination requirements consisting of both internal and external factors. This research was aimed at studying the effect of various external factors (temperature, humidity.etc.) affecting flax seed germination energy. The temperature varied in the range 16°C to 30°C, in increments of 2°C, as further increasing the temperature requires additional equipment and, consequently, additional energy consumption. The ambient humidity was maintained at 40, 60, 70, and 95%. The flax seeds were germinated for 36 hours till seedlings, up to 3 mm long, appeared. The germination energy was determined for each combination of the controlled factors. A mathematical model of the flaxseed germination process was constructed using the regression and correlation analysis methods. The model obtained determines the optimum germination modes. In the course of the experimental research, we applied experimental design techniques and mathematical processing of the experimental data. Using the computer programmes MathCad and Microsoft Excel optimized the flax seed germination and set its optimum modes. The constructed mathematical model makes it clear that the maximum germination energy 99.64% is achieved at the temperature 27.5°C and humidity 95%. The experimental and statistical models of germination of flax seeds have been obtained, describing the process with the correlation coefficient R = 0.96–0.99. The data obtained can be used to predict the quality parameters of flax seedlings and the energy consumption to obtain them.


2021 ◽  
Author(s):  
Aiju Meng ◽  
Daxing Wen ◽  
Chunqing Zhang

Spring maize is usually subjected to low-temperature stress during seed germination, which retards seedling growth even if under a suitable temperature. However, the mechanism underlying maize seed germination under low-temperature stress modulating seedling growth after being transferred to normal temperature is still ambiguous. In this study, we used two maize inbred lines with different low-temperature resistance (SM and RM) to investigate the mechanism. The results showed that the SM line had higher lipid peroxidation and lower total antioxidant capacity and germination percentage than the RM line under low-temperature stress, which indicated that the SM line was more vulnerable to low-temperature stress. Further transcriptome analysis revealed that seed germination under low-temperature stress caused down-regulation of photosynthesis related gene ontology (GO) terms in two lines. Moreover, the SM line displayed down-regulation of ribosome and superoxide dismutase (SOD) related genes, whereas genes involved in SOD and vitamin B6 were up-regulated in the RM line. Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis revealed that photosynthesis and antioxidant metabolism related pathways played important roles in seed germination in response to low-temperature stress, and the photosynthetic system displayed a higher damage degree in the SM line. Both qRT-PCR and physiological characteristics experiments showed similar results with transcriptome data. Taken together, we propose a model for maize seed germination in response to low-temperature stress.


2008 ◽  
Vol 8 (2) ◽  
pp. 63-68 ◽  
Author(s):  
Edson Simão ◽  
Massanori Takaki

The effect of light and temperature on Tibouchina mutabilis seed germination was analyzed by isothermic incubations in the range of 10 to 40 °C, with 5 °C intervals under both continuous white light (32.85 µmolm-2s-1) and darkness and alternating temperatures (15-20; 15-25; 15-30; 15-35; 20-25; 20-30; 20-35; 25-30; 25-35 and 30-35 °C) under both photoperiod of 12 hours and continuous darkness. The seeds of T. mutabilis need light to trigger the germination and no germination was observed in darkness. The range of optimum temperatures for germination was between 25 to 30 °C and the 20-25 °C alternating temperatures. These results indicate that T. mutabilis behaves as a pioneer species and daily alternating temperatures did not change the light sensitivity of seeds.


2003 ◽  
Vol 60 (3) ◽  
pp. 477-480 ◽  
Author(s):  
Warley Marcos Nascimento

Lettuce (Lactuca sativa L.) seed germination is strongly temperature dependent and under high temperatures, germination of most of genotypes can be erratic or completely inhibited. Lettuce seeds of 'Dark Green Boston' (DGB) were incubated at temperatures ranging from 15° to 35°C at light and dark conditions. Other seeds were imbibed in dark at 20°; 25°; 30°; and 35°C for 8 and 16 hours and then transferred to 20 or 35°C, in dark. Seeds were also incubated at constant temperature of 20° and 35 °C, in the dark, as control. In another treatment, seeds were primed for 3 days at 15°C with constant light. DGB lettuce seeds required light to germinate adequately at temperatures above 25°C. Seeds incubated at 20°C had 97% germination, whereas seeds incubated at 35°C did not germinate. Seeds imbibed at 20°C for 8 and 16 hours had germination. At 35°C, seeds imbibed initially at 20°C for 8 and 16 hours, had 89 and 97% germination, respectively. Seeds imbibed at 25°C for 16 hours, germinated satisfactory at 35°C. High temperatures of imbibition led to no germination. Primed and non-primed seeds had 100% germination at 20°C. Primed seeds had 100% germination at 35°C, whereas non-primed seeds germinate only 4%. The first hours of imbibition are very critical for lettuce seed germination at high temperatures.


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