Action of light and gibberellic acid on the growth of excised embryos from Phacelia tanacetifolia seeds

Planta ◽  
1970 ◽  
Vol 95 (4) ◽  
pp. 336-340 ◽  
Author(s):  
Shepley S. C. Chen
1963 ◽  
Vol 43 (4) ◽  
pp. 522-527 ◽  
Author(s):  
J. G. S. Trelawny ◽  
D. J. Ballantyne

Gibberellic acid (GA) at constant temperatures partially replaced the alternate temperatures required to break dormancy of intact seed of Bells of Ireland (Moluccella laevis L.). In the presence of GA optimum germination occurred at 10 °C. and declined to almost nil at 25 °C. When 2-naphthaleneacetic acid (NAA) at 10−5 M. was combined with GA the effect on germination at 20 °C. was synergistic. Higher concentrations of NAA antagonized the stimulatory effect of GA. All excised embryos germinated whether from chilled or unchilled seed. Embryos with attached endosperms from chilled seed showed a marked increase in germination over those from unchilled seed. GA induced 100 per cent germination of embryos with attached endosperms, irrespective of chilling, at 20 °C, but not at 25 °C. The presence of the pericarp completely prevented the germination of untreated seed at constant temperatures. Chilling whole seeds for 6 weeks at 5 °C. greatly enhanced penetration of external solutions to the embryo.


1967 ◽  
Vol 20 (6) ◽  
pp. 1237 ◽  
Author(s):  
EP Bachelard

Gibberellic acid promotes the germination of dormant seeds of some eucalypt species including Eucalyptus pauciflora Sieb. and E. delegatensis R. T. Baker. It was suggested that gibberellic acid may stimulate germination by promoting enzymatic weakening of the seed coat (Bachelard 1967) as described for Phacelia tanacetifolia seeds (Chen and Thimann 1964). Previously, Grose (1963) suggested dormancy of of E. delegatensis seeds might be due to the seed coat limiting gaseous exchange.


1993 ◽  
Vol 3 (4) ◽  
pp. 271-278 ◽  
Author(s):  
M. E. Foley ◽  
M. B. Nichols ◽  
S. P. Myers

AbstractIt has been proposed that gibberellic acid (GA3) promotes germination by overcoming restrictions in sugar production and utilization in afterripening-responsive dormant caryopses. While their germination rates were similar, germination commenced sooner in afterripened wild oat (Avena fatuaL.) caryopses than in dormant caryopses treated with GA3and dormant excised embryos treated with GA3plus fructose (Fru). Limited germination occurred in dormant excised embryos cultured with GA3alone. Carbohydrate concentrations were measured over time in dormant caryopses and excised embryos whose germination was induced with GA3and GA3plus Fru. The concentration of sucrose (Suc) in the endosperm declined prior to germination of dormant GA3-treated caryopses. Raffinose (Raf) family oligosaccharides in the embryos of dormant GA-treated caryopses remained relatively constant prior to and shortly after the onset of germination. In contrast, Raf family oligosaccharides in the embryos of afterripened caryopses declined prior to germination. Together this suggests Raf family oligosaccharide utilization is not associated with germinationper se.Increased starch levels, which occurred in dormant excised embryos treated with Fru and GA3plus Fru, were associated with dormancy because similar effects were not apparent in afterripened embryos cultured with Fru. An initial decline in the concentration of Raf family oligosaccharides in dormant embryos cultured with GA3or GA3plus Fru seems to be a result of the excision process. GA3appears to stimulate the germination of dormant embryos by enhancing the uptake or utilization of Fru. It appears that GA3and afterripening-induced changes in carbohydrate utilization in dormant caryopses are different.


1962 ◽  
Vol 40 (12) ◽  
pp. 1659-1673 ◽  
Author(s):  
G. M. Simpson ◽  
J. M. Naylor

Initiation of germination in excised embryos requires an exogenous energy source. Normally this is obtained from the endosperm. In dormant seeds the hydrolysis of starch is blocked despite the fact that dormant and non-dormant seeds contain similar amounts of α- and β-amylases. Alone or in combination the amylases are unable to break down raw endosperm starch granules to simple sugars in vitro. Exogenous maltase in combination with α-amylase hydrolyzes raw starch to glucose. Exogenous maltase eliminates the requirement for exogenous sugar. Examination of the maltase content of imbibed dormant and non-dormant seeds showed a marked increase in non-dormant seeds during the first 40 hours. This does not occur in dormant seeds unless they are treated with gibberellic acid. The results lead to the conclusion that an important effect of gibberellic acid is to induce the synthesis of maltase or in some way activate the preformed enzyme.


Nature ◽  
1961 ◽  
Vol 192 (4803) ◽  
pp. 679-680 ◽  
Author(s):  
J. M. NAYLOR ◽  
G. M. SIMPSON

Planta ◽  
1971 ◽  
Vol 100 (4) ◽  
pp. 365-369 ◽  
Author(s):  
Jerry M. Baskin ◽  
Carol C. Baskin

1971 ◽  
Vol 49 (10) ◽  
pp. 1833-1840 ◽  
Author(s):  
J. A. Simmonds ◽  
G. M. Simpson

The rates of oxygen consumption of dormant and non-dormant excised embryos of Avena fatua L. before germination are similar. Gibberellic acid (GA) treatment stimulates germination of dormant embryos without affecting oxygen consumption. Thus dormancy is not the result of restricted oxygen uptake. The fat content of dormant and non-dormant caryopses remains constant during germination. Dormant and non-dormant embryos have respiratory quotients near unity supporting the hypothesis that starch degradation occurs before germination. 6-Phosphogluconate dehydrogenase, a key enzyme of the pentose phosphate pathway, is present in dormant and non-dormant dry embryos but the pre-germination C6/C1 ratio of non-dormant embryos is markedly lower than that of dormant embryos, indicating a greater participation of the pentose phosphate pathway in the respiratory metabolism of non-dormant embryos. Release from dormancy is associated with a shift in metabolism from the glycolytic pathway to the pentose phosphate pathway. GA treatment, which stimulates germination of dormant embryos, causes a similar qualitative change in the oxidative metabolism of dormant embryos. Thus the action of GA is to cause the increased degradation of glucose via the pentose phosphate pathway, which is an essential step in the preparation for germination.


HortScience ◽  
2005 ◽  
Vol 40 (4) ◽  
pp. 1003D-1003
Author(s):  
Richard T. Olsen ◽  
Thomas G. Ranney ◽  
Zenaida Viloria

A series of studies were conducted to determine medium components necessary for ovule and embryo culture of ×Chitalpatashkentensis Elias & Wisura hybrids in order to improve recovery of interploid crosses. Ovules were collected at 2, 3, 4, 5, and 6 weeks after pollination (WAP) from selfed tetraploid × Chitalpa (S) and tetraploid × Chitalp × diploid Catalpabignonioides Walt. (3×) hybrids. Excised ovules were placed in petri dishes with Schenk and Hildebrandt (SH) medium and 0.7% agar, with or without coconut-water (2%) and three sucrose concentrations (20, 40, or 80 g·L-1). No ovules germinated for either cross in any treatment at 2, 3, and 4 WAP. Selfed ovules germinated at 5 WAP, in both 20 and 40 g·L-1 sucrose. At 6 WAP, 3× ovules germinated in 20 g·L-1 sucrose. Coconut water provided no apparent benefit. Embryos were apparent at 6 WAP, so a new study was initiated to compare ovule vs. embryo culture at this sample date. Excised embryos germinated in greater percentages than ovules, in all treatment combinations at 6 WAP. Germination in 80 g·L-1 sucrose was observed only for S embryos without coconut water. Greatest 3× germination (16.7%) was observed for embryos in 20 g·L-1 sucrose without coconut water. A final study was conducted to investigate the effect of gibberellic acid (GA3) on embryo germination. Embryos were harvested at 7 WAP for both crosses and grown in SH medium supplemented with 20 g·L-1 sucrose and 0, 1, 2, or 4 μm GA3. The addition of GA3, regardless of concentration, increased germination from 30.6% to 99.1% for S embryos and from 11.1% to 99.1% for 3× embryos.


2005 ◽  
Vol 15 (4) ◽  
pp. 349-356 ◽  
Author(s):  
Carol C. Baskin ◽  
Jerry M. Baskin ◽  
Alvin Yoshinaga ◽  
Ken Thompson

This study addressed the difficulty of germinating drupelets (hereafter seeds) in the multi-seeded stony dispersal units (drupes) of Leptecophylla tameiameiae (Ericaceae). Embryos in fresh seeds were 77% the length of the endosperm, and seeds inside the intact drupes imbibed water. We monitored germination at 15/6, 20/10 and 25/15°C for 162 weeks, after which each drupe was cut open and ungerminated seeds counted. Drupes contained 1–6 seeds, and the total number of seeds in all treatments and controls was 1977, with 20, 29, 25, 18, 7 and <1% of them occurring in one-, two-, three-, four-, five- and six-seeded drupes, respectively. The percentage of seeds germinating in one-, two-, three-, four-, five- and six-seeded drupes was 74, 66, 65, 72, 56 and 0, respectively. Neither warm nor cold stratification for 6 or 12 weeks significantly increased germination percentages, compared to controls incubated continuously at 25/15°C for 162 weeks, where 72% of the seeds in the drupes germinated. At 25/15°C, 24–49 weeks were required for 20% of the seeds to germinate. Warm followed by cold stratification did not promote germination, and there was no widening of the temperature range for germination. Like seeds of other species known to have deep physiological dormancy (PD), those of L. tameiameiae required extended periods of time (16 to ≥162 weeks) to come out of dormancy and germinate, gibberellic acid (GA3) did not promote germination and excised embryos failed to grow. Thus, we conclude that seeds of L. tameiameiae have deep PD. However, unlike seeds of other species with deep PD, those of L. tameiameiae required an extensive period of warm rather than of cold stratification to come out of dormancy. It is suggested that a subtype a (seeds require a long period of cold stratification to come out of dormancy) and a subtype b (seeds require a long period of exposure to warm stratification to come out of dormancy) of deep PD be recognized in the Nikolaeva formula system for classifying seed dormancy.


1962 ◽  
Vol 37 (5) ◽  
pp. 579-583 ◽  
Author(s):  
L. G. Paleg ◽  
D.H.B. Sparrow ◽  
A. Jennings

Sign in / Sign up

Export Citation Format

Share Document