Academic literature on the topic 'Hydrothermal after-ripening time'

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Journal articles on the topic "Hydrothermal after-ripening time"

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Christensen, Maren, Susan E. Meyer, and Phil S. Allen. "A hydrothermal time model of seed after-ripening in Bromus tectorum L." Seed Science Research 6, no. 4 (December 1996): 155–64. http://dx.doi.org/10.1017/s0960258500003214.

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AbstractBromus tectorum L. is an invasive winter annual grass with seeds that lose dormancy through the process of dry after-ripening. This paper proposes a model for after-ripening of B. tectorum seeds based on the concept of hydrothermal time. Seed germination time course curves are modelled using five parameters: a hydrothermal time constant, the fraction of viable seeds in the population, base temperature, mean base water potential and the standard deviation of base water potentials in the population. It is considered that only mean base water potential varies as a function of storage duration and incubation temperature following after-ripening. All other parameters are held constant throughout after-ripening and at all incubation temperatures. Data for model development are from seed germination studies carried out at four water potentials (0, −0.5, −1.0 and −1.5 MPa) at each of two constant incubation temperatures (15 and 25°C) following different storage intervals including recently harvested, partially after-ripened (stored for 4, 9 or 16 weeks at 20°C) and fully after-ripened (stored for 14 weeks at 40°C). The model was fitted using a repeated probit regression method, and for the two seed populations studied gave R2 values of 0.898 and 0.829. Germination time course curves predicted by the model generally had a good fit when compared with observed curves at the incubation temperature/water potential treatment combinations for different after-ripening intervals. Changes in germination time course curves during after-ripening of B. tectorum can largely be explained by decreases in the mean base water potential. The simplicity and good fit of the model give it considerable potential for extension to simulation of after-ripening under field conditions.
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Bair, Necia B., Susan E. Meyer, and Phil S. Allen. "A hydrothermal after-ripening time model for seed dormancy loss in Bromus tectorum L." Seed Science Research 16, no. 1 (March 2006): 17–28. http://dx.doi.org/10.1079/ssr2005237.

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After-ripening, the loss of dormancy under dry conditions, is associated with a decrease in mean base water potential for germination ofBromus tectorumL. seeds. After-ripening rate is a linear function of temperature above a base temperature, so that dormancy loss can be quantified using a thermal after-ripening time (TAR) model. To incorporate storage water potential into TAR, we created a hydrothermal after-ripening time (HTAR) model. Seeds from twoB. tectorumpopulations were stored under controlled temperatures (20 or 30 °C) and water potentials (−400 to −40 MPa). Subsamples were periodically removed from each storage treatment and incubated at 15 or 25 °C to determine germination time courses. Dormancy status (mean base water potential) was calculated from each time course using hydrothermal time equations developed for each seed collection. Seeds stored at −400 MPa did not after-ripen. At water potentials from −400 to −150 MPa, the rate of after-ripening increased approximately linearly with increasing water potential. Between −150 and −80 MPa, there was no further increase in after-ripening rate, while at −40 MPa seeds did not after-ripen and showed loss of vigour. These results suggest that the concept of critical water potential thresholds, previously shown to be associated with metabolic activity and desiccation damage in partially hydrated seeds, is also relevant to the process of after-ripening. The HTAR model generally improved field predictions of dormancy loss when the soil was very dry. Reduced after-ripening rate under such conditions provides an ecologically relevant explanation of how seeds prolong dormancy at high summer soil temperatures.
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Alvarado, Veria, and Kent J. Bradford. "Hydrothermal time analysis of seed dormancy in true (botanical) potato seeds." Seed Science Research 15, no. 2 (June 2005): 77–88. http://dx.doi.org/10.1079/ssr2005198.

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As seed dormancy is released within a seed population, both the rate and percentage of germination increase progressively with increasing dose of a dormancy-breaking treatment or condition. Population-based models can account for this behaviour on the basis of shifting response thresholds as dormancy is alleviated. In particular, hydrothermal time analysis of germination sensitivity to water potential (Ψ) and temperature (T) can describe these features of seed behaviour. We used the hydrothermal time model to analyse the effects of dormancy-breaking treatments on germination of dormant true (botanical) potato (Solanum tuberosumL.) seeds (TPS). After-ripening (37°C and 4% seed moisture content) of TPS for 7 or 30 days partially or fully alleviated primary dormancy. The median base water potential required to prevent germination [Ψb(50)] decreased from –0.25 MPa in control seeds to –0.87 MPa and –1.83 MPa after 7 and 30 days of after-ripening, respectively. In contrast, the base temperature for germination (Tb) was relatively unaffected (0–3.3°C). Fluridone (50 μM), an inhibitor of abscisic acid (ABA) biosynthesis, also promoted germination of dormant TPS and lowered Ψb(50), indicating a role forde novosynthesis of ABA during dormancy maintenance. Moist chilling (3 days at 4°C) or gibberellin (100 μM) alleviated secondary dormancy and lowered Ψb(50) values from –0.08 MPa to –0.36 and –0.87 MPa, respectively. The hydrothermal time model allows quantification of dormancy levels and explains why changes in germination speed and percentage are closely correlated during dormancy alleviation.
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Meyer, Susan E., Susan B. Debaene-Gill, and Phil S. Allen. "Using hydrothermal time concepts to model seed germination response to temperature, dormancy loss, and priming effects in Elymus elymoides." Seed Science Research 10, no. 3 (September 2000): 213–23. http://dx.doi.org/10.1017/s0960258500000246.

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AbstractHydrothermal time (HTT) describes progress toward seed germination under various combinations of incubation water potential ( ) and temperature (T). To examine changes in HTT parameters during dormancy loss, seeds from two populations of the bunchgrass Elymus elymoides were incubated under seven temperature regimes following dry storage at 10, 20 and 30°C for intervals from 0 to 16 weeks. Fully after-ripened seeds were primed for 1 week at a range of s. Data on germination rate during priming were used to obtain a HTT equation for each seed population, while data obtained following transfer to water were used to calculate HTT accumulation during priming. HTT equations accurately predicted germination time course curves if mean base water potential, b(50), was allowed to vary with temperature. b(50) values increased linearly with temperature, explaining why germination rate does not increase with temperature in this species. b(50) showed a linear decrease as a function of thermal time in storage. Slopes for the T × b(50) relationship did not change during after-ripening. This thermal after-ripening time model was characterized by a single base temperature and a constant slope across temperatures for each collection. Because the difference between initial and final b(50)s was uniform across tempera-tures, the thermal after-ripening requirement was also a constant. When seeds were primed for 1 week at −4 to −20 MPa, accumulation of HTT was a uniform 20% of the total HTT requirement. When primed at 0 to −4 MPa, HTT accumulation decreased linearly with decreasing priming potential, and a hydrothermal priming time model using a constant minimum priming potential adequately described priming effects. Use of these simple HTT relationships will facilitate modelling of germination phenology in the field.
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Gallagher, Robert S., Kathryn J. Steadman, and Andrew D. Crawford. "Alleviation of dormancy in annual ryegrass (Lolium rigidum) seeds by hydration and after-ripening." Weed Science 52, no. 6 (December 2004): 968–75. http://dx.doi.org/10.1614/ws-04-075r.

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The effect of hydration (priming) treatment on dormancy release in annual ryegrass seeds from two populations was investigated. Hydration duration, number, and timing with respect to after-ripening were compared in an experiment involving 15 treatment regimens for 12 wk. Seeds were hydrated at 100% relative humidity for 0, 2, or 10 d at Weeks 1, 6, or 12 of after-ripening. Dormancy status was assessed after each hydration treatment by measuring seed germination at 12-hourly alternating 25/15 C (light/dark) periods using seeds directly from the hydration treatment and seeds subjected to 4 d postpriming desiccation. Seeds exposed to one or more hydration events during the 12 wk were less dormant than seeds that remained dry throughout after-ripening. The longer hydration of 10 d promoted greater dormancy loss than either a 2-d hydration or no hydration. For the seed lot that was most dormant at the start of the experiment, two or three rather than one hydration event or a hydration event earlier rather than later during after-ripening promoted greater dormancy release. These effects were not significant for the less-dormant seed lot. For both seed lots, the effect of a single hydration for 2 d at Week 1 or 6 of after-ripening was not manifested until the test at Week 12 of the experiment, suggesting that the hydration events alter the rate of dormancy release during subsequent after-ripening. A hydrothermal priming time model, usually used for modeling the effect of priming on germination rate of nondormant seeds, was successfully applied to dormancy release resulting from the hydration treatments.
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Hawkins, K. K., P. S. Allen, and S. E. Meyer. "Secondary dormancy induction and release inBromus tectorumseeds: the role of temperature, water potential and hydrothermal time." Seed Science Research 27, no. 1 (January 10, 2017): 12–25. http://dx.doi.org/10.1017/s0960258516000258.

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AbstractSeeds of the winter annualBromus tectorumlose primary dormancy in summer and are poised to germinate rapidly in the autumn. If rainfall is inadequate, seeds remain ungerminated and may enter secondary dormancy under winter conditions. We quantified conditions under which seeds enter secondary dormancy in the laboratory and field and also examined whether contrastingB. tectorumgenotypes responded differently to dormancy induction cues. The study also extends previous hydrothermal time models for primary dormancy loss and germination timing inB. tectorumby using similar models to account for induction and loss of secondary dormancy. Maximum secondary dormancy was achieved in the laboratory after 4 weeks at –1.0 MPa and 5°C. Seeds in the field became increasingly dormant through exposure to temperatures and water potentials in this range, confirming laboratory results. They were released from dormancy through secondary after-ripening the following summer. Different genotypes showed contrasting responses to dormancy induction cues in both laboratory and field. To examine secondary dormancy induction and release in the field in terms of hydrothermal time parameters, we first created a model that allowed mean base water potential (Ψb(50)) to vary while holding other hydrothermal time parameters constant, as in models for primary dormancy loss under dry conditions. The second model allowed all three model parameters to vary through time, to account for changes (e.g. hydrothermal time accumulation) that could occur simultaneously with dormancy induction in imbibed seeds. Shifts in Ψb(50) could explain most changes in dormancy status for seeds retrieved from the field, except during the short period prior to dormancy induction, when hydrothermal time was accumulating. This study illustrates that hydrothermal modelling, and specifically changes in Ψb(50), can be used to characterize secondary dormancy induction and loss inB. tectorum.
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Huang, Wei, Yujiang Wang, Shicheng Wei, Bo Wang, Yi Liang, Yuwei Huang, and Binshi Xu. "Effect of Reaction Time on Microwave Absorption Properties of Fe3O4 Hollow Spheres Synthesized via Ostwald Ripening." Materials 12, no. 18 (September 10, 2019): 2921. http://dx.doi.org/10.3390/ma12182921.

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Hollow magnetic structures have great potential to be used in the microwave absorbing field. Herein, Fe3O4 hollow spheres with different levels of hollowness were synthesized by the hydrothermal method under Ostwald ripening effect. In addition to their microstructures, the microwave absorption properties of such spheres were investigated. The results show that the grain size and hollowness of Fe3O4 hollow spheres both increase as the reaction time increases. With increasing hollowness, the attenuation ability of electromagnetic wave of Fe3O4 spheres increases first and then decreases, finally increases sharply after the spheres break down. Samples with strong attenuation ability can achieve good impedance matching, which it does preferentially as the absorber thickness increases. Fe3O4 hollow spheres show the best microwave absorption performance when the reaction time is 24 h. The minimum reflection loss (RL (min)) can reach −40 dB, while the thickness is only 3.2 mm.
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Allen, Phil S., and Susan E. Meyer. "Ecological aspects of seed dormancy loss." Seed Science Research 8, no. 2 (June 1998): 183–92. http://dx.doi.org/10.1017/s0960258500004098.

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AbstractAdvances in seed biology include progress in understanding the ecological significance of seed dormancy mechanisms. This knowledge is being used to make more accurate predictions of germination timing in the field. For several wild species whose seedlings establish in spring, seed populations show relevant variation that can be correlated with habitat conditions. Populations from severe winter sites, where the major risk to seedlings is frost, tend to have long chilling requirements or to germinate very slowly at low temperatures. Populations from warmer sites, where the major risk is drought, are non-dormant and germinate very rapidly under these same conditions. Seed populations from intermediate sites exhibit variation in dormancy levels, both among and within plants, which spreads germination across a considerable time period. For grasses that undergo dry after-ripening, seed dormancy loss can be successfully modelled using hydrothermal time. Dormancy loss for a seed population is associated with a progressive downward shift in the mean base water potential, i.e., the water potential below which half of the seeds will not germinate. Other parameters (hydrothermal time requirement, base temperature and standard deviation of base water potentials) tend to be constant through time. Simulation models for predicting dormancy loss in the field can be created by combining measurements of seed zone temperatures with equations that describe changes in mean base water potential as a function of temperature. Successful validation of these and other models demonstrates that equations based on laboratory data can be used to predict dormancy loss under widely fluctuating field conditions. Future progress may allow prediction of germination timing based on knowledge of intrinsic dormancy characteristics of a seed population and long-term weather patterns in the field.
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MIGUEL, ANA CAROLINA ALMEIDA, JOSÉ FERNANDO DURIGAN, KELLY MAGALHÃES MARQUES, CRISTIANE MARIA ASCARI MORGADO, and ANTONIO SERGIO FERRAUDO. "PREVENTION OF CHILLING INJURY IN 'TOMMY ATKINS' MANGOES PREVIOUSLY STORED AT 5 ºC, USING HEAT TREATMENT AND RADIATION UV (UV-C)." Revista Brasileira de Fruticultura 38, no. 1 (February 2016): 53–63. http://dx.doi.org/10.1590/0100-2945-123/14.

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ABSTRACT The objective of this study was to evaluate the effect of heat treatment and ultraviolet radiation (UV-C) in the prevention of chilling injury in mangoes cv. Tommy Atkins previously stored or not under injury condition after their transference to ambient condition. Fruits were divided into groups: two were hydrothermally treated (46.1 ºC/90 min; 55 ºC/5 min) and two were exposed to UV-C radiation (1.14 kJ m-2; 2.28 kJ m-2). These groups were stored under chilling injury conditions (5 ºC for 14 days), as established in preliminary tests. Other untreated groups were stored at 12 ºC or 5 ºC. After the storage period, they were transferred to ambient conditions (21.9 ºC; 55% RH) and the quality was evaluated. All the data were submitted to multivariate analysis as the tool to verify the simultaneous effect of the treatments under the quality parameters. The multivariate analysis indicated that the hydrothermal treatments at 46.1 °C/90 min and 55 °C/5 min and the UV-C radiation at doses of 1.14 kJ m-2 and 2.28 kJ m-2 were effective in minimized the symptoms of chilling injury in mangoes ‘Tommy Atkins’ stored at 5 °C for 14 days. However, after their transference to environmental condition at 21.9 °C, only the UV-C kept this control, especially at a dose of 2.28 kJ m-2. This treatment did not prevent the development of the characteristic color or affected the normal ripening and allowed the conservation of fruit for a period of 14 days at 5 °C, plus seven days of storage at environmental condition, which corresponds to the shipping transportation plus the time for sale.
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Dissertations / Theses on the topic "Hydrothermal after-ripening time"

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Bair, Necia Beck. "A Hydrothermal After-ripening Time Model of Seed Dormancy Loss in Bromus tectorum." BYU ScholarsArchive, 2004. https://scholarsarchive.byu.edu/etd/533.

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After-ripening, the process of seed dormancy loss in dry storage is associated with a decrease in the mean base water potential, one of the parameters of hydrothermal time. The rate of change of the mean base water potential is assumed to be a linear function of temperature above a specific base temperature and as a result can be described by a thermal after-ripening (TAR) time model, an extension of hydrothermal modelling. The thermal requirement for after-ripening is the thermal time necessary for the modelling base water potential of the seed to shift from its original value to its final value. In order to include the effects of water potential on the rate of dormancy loss, a hydrothermal after-ripening (HTAR) time model was developed. Laboratory and field studies were conducted using seeds of Bromus tectorum. These studies identified four important ranges of water potential that influence the rate of dormancy loss. The ranges are identified as follows: seeds experiencing soil water potentials seeds experiencing soil water potentials <-400 MPa do not after-ripen, between -400 MPa and -150 MPa seeds after-ripen as a function of temperature (T) and water potential (Ψ), seeds experiencing water potentials >-150 MPa after-ripen as a linear function of temperature, and somewhere above -40 MPa seeds are too wet to after-ripen. These ranges suggest that specific reaction thresholds associated with non-fully imbibed seeds also apply to the process of after-ripening. The HTAR model for B. tectorum seeds generally improved predictions of dormancy loss in the field under soil conditions that were too dry for TAR alone. Reduced after-ripening rate under extremely dry conditions is ecologically relevant in explaining how seeds may prolong dormancy under high soil temperature conditions.
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Bair, Necia B. "A hydrothermal after-ripening time model of seed dormancy loss in Bromus tectorum /." Diss., CLICK HERE for online access, 2004. http://contentdm.lib.byu.edu/ETD/image/etd487.pdf.

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