Literature DB >> 16668727

Quantitative models characterizing seed germination responses to abscisic Acid and osmoticum.

B R Ni1, K J Bradford.   

Abstract

Mathematical models were developed to characterize the physiological bases of the responses of tomato (Lycopersicon esculentum Mill. cv T5) seed germination to water potential (psi) and abscisic acid (ABA). Using probit analysis, three parameters were derived that can describe the germination time courses of a seed population at different psi or ABA levels. For the response of seed germination to reduced psi, these parameters are the mean base water potential ( psi(b), MPa), the standard deviation of the base water potential among seeds in the population (sigma(psib), MPa), and the "hydrotime constant" (theta(H), MPa.h). For the response to ABA, they are the log of the mean base ABA concentration ([unk]ABA(b), m), the standard deviation of the base ABA concentration among seeds in the population (sigma(ABA) (b), log[m]), and the "ABA-time constant" (theta(ABA), log[m].h). The values of psi(b) and [unk]ABA(b) provide quantitative estimates of the mean sensitivity of germination rate to psi or ABA, whereas sigma(psi) (b) and sigma(ABA) (b) account for the variation in sensitivity among seeds in the population. The time constants, theta(H) and theta(ABA), indicate the extent to which germination rate will be affected by a given change in psi or ABA. Using only these parameters, germination time courses can be predicted with reasonable accuracy at any medium psi according to the equation probit(g) = [psi - (theta(H)/t(g)) - psi(b)]/sigma(psib), or at any ABA concentration according to the equation probit(g) = [log[ABA] - (theta(ABA)/t(g)) - log[[unk]ABA(b)]]/sigma(ABA) (b), where t(g) is the time to radicle emergence of percentage g, and ABA is the ABA concentration (m) in the incubation solution. In the presence of both ABA and reduced psi, the same parameters can be used to predict seed germination time courses based upon strictly additive effects of psi and ABA in delaying the time of radicle emergence. Further analysis indicates that ABA and psi can act both independently and interactively to influence physiological processes preparatory for radicle growth, such as the accumulation of osmotic solutes in the embryo. The models provide quantitative values for the sensitivity of germination to ABA or psi, allow evaluation of independent and interactive effects of the two factors, and have implications for understanding how ABA and psi may regulate growth and development.

Entities:  

Year:  1992        PMID: 16668727      PMCID: PMC1080308          DOI: 10.1104/pp.98.3.1057

Source DB:  PubMed          Journal:  Plant Physiol        ISSN: 0032-0889            Impact factor:   8.340


  10 in total

1.  A water relations analysis of seed germination rates.

Authors:  K J Bradford
Journal:  Plant Physiol       Date:  1990-10       Impact factor: 8.340

Review 2.  Gene expression in response to abscisic acid and osmotic stress.

Authors:  K Skriver; J Mundy
Journal:  Plant Cell       Date:  1990-06       Impact factor: 11.277

3.  Water Relations of Seed Development and Germination in Muskmelon (Cucumis melo L.) : III. Sensitivity of Germination to Water Potential and Abscisic Acid during Development.

Authors:  G E Welbaum; T Tissaoui; K J Bradford
Journal:  Plant Physiol       Date:  1990-04       Impact factor: 8.340

4.  Evaluation of the water potentials of solutions of polyethylene glycol 8000 both in the absence and presence of other solutes.

Authors:  B E Michel
Journal:  Plant Physiol       Date:  1983-05       Impact factor: 8.340

5.  ABA Levels and Sensitivity in Developing Wheat Embryos of Sprouting Resistant and Susceptible Cultivars.

Authors:  M Walker-Simmons
Journal:  Plant Physiol       Date:  1987-05       Impact factor: 8.340

6.  Water Deficit and Abscisic Acid Cause Differential Inhibition of Shoot versus Root Growth in Soybean Seedlings : Analysis of Growth, Sugar Accumulation, and Gene Expression.

Authors:  R A Creelman; H S Mason; R J Bensen; J S Boyer; J E Mullet
Journal:  Plant Physiol       Date:  1990-01       Impact factor: 8.340

7.  Effect of Water Stress, Seed Coat Restraint, and Abscisic Acid upon Different Germination Capabilities of Two Tomato Lines at Low Temperature.

Authors:  A Liptay; P Schopfer
Journal:  Plant Physiol       Date:  1983-12       Impact factor: 8.340

8.  Control of Seed Germination by Abscisic Acid : II. Effect on Embryo Water Uptake in Brassica napus L.

Authors:  P Schopfer; C Plachy
Journal:  Plant Physiol       Date:  1984-09       Impact factor: 8.340

9.  Control of Seed Germination by Abscisic Acid : III. Effect on Embryo Growth Potential (Minimum Turgor Pressure) and Growth Coefficient (Cell Wall Extensibility) in Brassica napus L.

Authors:  P Schopfer; C Plachy
Journal:  Plant Physiol       Date:  1985-03       Impact factor: 8.340

10.  In Vivo Inhibition of Seed Development and Reserve Protein Accumulation in Recombinants of Abscisic Acid Biosynthesis and Responsiveness Mutants in Arabidopsis thaliana.

Authors:  M Koornneef; C J Hanhart; H W Hilhorst; C M Karssen
Journal:  Plant Physiol       Date:  1989-06       Impact factor: 8.340

  10 in total
  20 in total

1.  Sensitivity Thresholds and Variable Time Scales in Plant Hormone Action.

Authors:  K. J. Bradford; A. J. Trewavas
Journal:  Plant Physiol       Date:  1994-08       Impact factor: 8.340

2.  Predicting changes in dormancy level in natural seed soil banks.

Authors:  Diego Batlla; Roberto Luis Benech-Arnold
Journal:  Plant Mol Biol       Date:  2010-01-21       Impact factor: 4.076

3.  Germination responses to temperature and water potential in Jatropha curcas seeds: a hydrotime model explains the difference between dormancy expression and dormancy induction at different incubation temperatures.

Authors:  Liliana B Windauer; J Martinez; D Rapoport; D Wassner; Roberto Benech-Arnold
Journal:  Ann Bot       Date:  2011-09-13       Impact factor: 4.357

4.  Regulation of Em Gene Expression in Rice : Interaction between Osmotic Stress and Abscisic Acid.

Authors:  R M Bostock; R S Quatrano
Journal:  Plant Physiol       Date:  1992-04       Impact factor: 8.340

5.  Germination and Dormancy of Abscisic Acid- and Gibberellin-Deficient Mutant Tomato (Lycopersicon esculentum) Seeds (Sensitivity of Germination to Abscisic Acid, Gibberellin, and Water Potential).

Authors:  B. R. Ni; K. J. Bradford
Journal:  Plant Physiol       Date:  1993-02       Impact factor: 8.340

6.  Class I chitinase and beta-1,3-glucanase are differentially regulated by wounding, methyl jasmonate, ethylene, and gibberellin in tomato seeds and leaves.

Authors:  Chun-Ta Wu; Kent J Bradford
Journal:  Plant Physiol       Date:  2003-09       Impact factor: 8.340

7.  Endo-[beta]-Mannanase Activity from Individual Tomato Endosperm Caps and Radicle Tips in Relation to Germination Rates.

Authors:  D. W. Still; K. J. Bradford
Journal:  Plant Physiol       Date:  1997-01       Impact factor: 8.340

8.  A Single-Seed Assay for Endo-[beta]-Mannanase Activity from Tomato Endosperm and Radicle Tissues.

Authors:  D. W. Still; P. Dahal; K. J. Bradford
Journal:  Plant Physiol       Date:  1997-01       Impact factor: 8.340

9.  Relationship of Endo-[beta]-D-Mannanase Activity and Cell Wall Hydrolysis in Tomato Endosperm to Germination Rates.

Authors:  P. Dahal; D. J. Nevins; K. J. Bradford
Journal:  Plant Physiol       Date:  1997-04       Impact factor: 8.340

10.  Class I [beta]-1,3-Glucanases in the Endosperm of Tobacco during Germination.

Authors:  G. Leubner-Metzger; C. Frundt; R. Vogeli-Lange; F. Meins
Journal:  Plant Physiol       Date:  1995-11       Impact factor: 8.340

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