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By identifying the factors that initiate seed dormancy release, we can reliably predict whether a seed will remain dormant within or exit the seed bank and become a seedling. With regard to annual weed species, assessing which factors efficiently break seed dormancy is critical for estimating the number of weed seeds that will develop into problematic weeds. To better understand dormancy breaking in Redroot pigweed (Amaranthus retroflexus), dormant seeds were treated with cold stratification (4°C for 30 days), application of gibberellic acid (at 500, 1000, 1500, and 2000 parts per million), ultrasound (for 10, 20, 30, and 40 min), soaking in hot water (90°C for 3, 5, 7, and 10 min), and 98% sulfuric acid (for 1, 2, and 3 min). The results showed that Redroot pigweed seed dormancy was effectively broken by cold stratification, gibberellic acid, and ultrasound. Short treatments with hot water had minimal effect while longer times or treatment with sulfuric acid stopped seed germination. In addition to germination percentage, germination rate, plumule length, radicle length, seedling length, seedling dry weight, and seed vigor index were also measured; similarly, application of gibberellic acid had the most significant effect on these parameters. The results of this study add to our knowledge of what processes effectively or ineffectively break Redroot pigweed seed dormancy and promote growth. [ABSTRACT FROM AUTHOR]

Summary: Dormant seeds of oilseed rape (OSR) can persist in the soil and cause OSR volunteers in subsequent crops. Several approaches were tested in the laboratory and in the field to determine whether dormancy induction and seed persistence can be reduced by using dormancy‐breaking exogenous compounds. In a laboratory experiment, OSR seeds were coated with KNO3, micronutrients, or gibberellic acid (GA) prior to a secondary dormancy test. In a field experiment, seeds were coated in a manner analogous to the laboratory experiment, and then buried 10 cm deep in the soil for 2.5 months. In a practical demonstration, OSR plants were sprayed with either urea ammonium nitrate (UAN) or a commercial product containing GA prior to seed maturity. Seed coating (laboratory and field experiments) reduced secondary dormancy and seed persistence in the field by up to 99%. The efficiency of the treatments for mitigating secondary dormancy (laboratory and field experiments) in decreasing order was GA > micronutrients > KNO3 > control. With pre‐maturity spraying (practical demonstration), UAN reduced primary dormancy by up to 77% and the development of secondary dormancy by up to 38%; GA had no effect. Dormancy and seed persistence of OSR seeds may be reduced by a pre‐maturity UAN treatment of OSR mother plants, or by applying appropriate exogenous compounds to OSR seeds. [ABSTRACT FROM AUTHOR]

The changes of ascorbic acid, dehydroascorbic acid, and glutathione content and related enzyme activities were studied in apple buds during dormancy and thidiazuron-induced bud break. An increase in ascorbic acid, reduced form of glutathione (GSH), total glutathione, total non-protein thiol (NPSH) and non-glutathione thiol (RSH) occurred as a result of induction by thidiazuron during bud break, whereas dehydroascorbic acid and oxidized glutathione (GSSG) decreased during the same period. Thidiazuron also enhanced the ratio of GSH/GSSG, and activities of ascorbate free radical reductase (AFR; EC 1.6.5.4), ascorbate peroxidase (EC 1.11.1.11), dehydroascorbate reductase (DHAR; EC 1.8.5.1) and glutathione reductase (GR; EC 1.6.4.2). The ascorbic acid content and the activities of AFR, ascorbate peroxidase, and DHAR peaked when buds were in the side green or green tip stage just prior to the start of rapid expansion, and declined thereafter. The GSH, NPSH, RSH, ratio of GSH/GSSG, and activities of GR increased steadily during bud development. [ABSTRACT FROM AUTHOR]

Changes in ribosome population, RNA species and DNA composition in flower buds of apples (Malus pumila Mill. cvs Ralls and White winter pearmain) were investigated during breaking of dormancy and development. After bursting of flower buds, total ribosomes increased approximately 4-fold, and the polyribosomal fraction increased from 66% to 94% of total ribosomes. The newly synthesized ribosomes were identified by incorporation of radioactive precursor. The observed decrease in specific radioactivity of the monoribosomes is caused by the recruitment of mononribosomes into polyribosomes after breaking of dormancy. In both cultivars, the 25S and 18S rRNA peaks increased to a high level on April 8. The peaks of low molecular weight RNA were apparently increased after initial swelling of the flower buds. The DNA of flower buds was separated into three bands by electrophoresis. The median band is the main band of nuclear DNAs. The ahead band and the slow-moving band are satellite components of nuclear DNAs, and they obviously rose after initial swelling of the flower buds. On April 8, when the flower buds had opened, two other small DNA bands could be detected. These results suggest that the changes in level of different ribosome populations, RNA species and DNA composition are related to dormancy breaking development of apple flower buds. [ABSTRACT FROM AUTHOR]