We examined whether spectrally active phytochrome A (PhyA) and phytochrome B (PhyB) play specific roles in the induction of seed germination in Arabidopsis thaliana (L.) Heynh., using PhyA- and PhyB-null mutants, fre1-1 (A. Nagatani, J.W. Reed, J. Chory [1993] Plant Physiol 102: 269-277) and hy3-Bo64 (J. Reed, P.Nagpal, D.S. Poole, M. Furuya, J. Chory [1993] Plant Cell 5: 147-157). When dormant...

In order to determine the best developmental stage of soybean at which maximum seed quality is attained under different shadings (S1, S2, S3: 0, 35 and 75% shade, respectively) and irrigation treatments (I1, I2, I3, I4: irrigation after 60, 90, 120 and 150 mm evaporation from class A pan, respectively), two split plot experiments using randomized complete block design with three replications we...

The phytohormones abscisic acid (ABA) and gibberellins (GAs) are the primary signals that regulate seed dormancy and germination. In this study, we investigated the role of a double APETALA2 repeat transcription factor, CHOTTO1 (CHO1), in seed dormancy, germination, and phytohormone metabolism of Arabidopsis (Arabidopsis thaliana). Wild-type seeds were dormant when freshly harvested seeds were ...

Reactive oxygen species (ROS) promote the germination of several seeds, and antioxidants suppress it. However, questions remain regarding the role and production mechanism of ROS in seed germination. Here, we focused on NADPH oxidases, which produce ROS. After imbibition, NADPH oxidase mRNAs were expressed in the embryo and in aleurone cells of barley seed; these expression sites were consisten...

Galactinol synthase (GolS) catalyzes the first and rate limiting step of Raffinose Family Oligosaccharide (RFO) biosynthetic pathway, which is a highly specialized metabolic event in plants. Increased accumulation of galactinol and RFOs in seeds have been reported in few plant species, however their precise role in seed vigor and longevity remain elusive. In present study, we have shown that ga...

OBJECTIVE To develop a protocol for breaking of seed dormancy and increasing the seed germination rate of Bunium persicum. METHODS The seeds were treated with 3.1, 6.3, 12.5, 25, 50 and 100 µmol/L of benzyl aminopurine, gibberellic acid (GA3), thidiazuron (TDZ) and forchlorfenuron. Then, seeds were transferred to two different temperature conditions including room temperature (25 °C) and chil...

Assessment of dormancy inception, maintenance and release was studied for artificially dried immature seeds harvested throughout seed development in the barley cv. Triumph and its mutant line TL43. Each was grown in Spain and Scotland under low and high dormancy inducing conditions, respectively. Both TL43 and Triumph followed a similar pattern of release from dormancy across the seasons, altho...

Phase II of germination represents a key developmental stage of plant growth during which imbibed seeds either enter stage III of germination, completing the germination process via radicle protrusion, or remain dormant. In this study, we analyzed the influence of the peroxisomal ATP-binding cassette transporter COMATOSE (CTS) on the postimbibition seed transcriptome of Arabidopsis (Arabidopsis...

Seed dormancy and endozoochorous dispersal have important effects on population dynamics, i.e. seed bank formation, spatial and temporal bethedging, avoidance of crowding and decreased sib-competition. Seeds having primary dormancy do not germinate, even if adequate environmental and dispersal conditions are met, until an after-ripening period is completed. This study examined the effects on ge...

Seed lots with the genetic background of ‘Baroda’ and ‘Marketer’ cucumber (Cucumis sativus L.) containing all possible combinations (DF Df, Dfdf, dfdf) of df (which increases dormancy) and Df (wild type) were used. Dormancy was not solely due to the genotype dfdf and clear effects of genetic background were apparent. The df allele in the homozygous state induced a strong dormancy in ‘Baroda’, b...