Effects of temperature, light and stratification on seed germination of Wollemi pine (Wollemia nobilis, Araucariaceae)

2001 ◽  
Vol 49 (6) ◽  
pp. 699 ◽  
Author(s):  
C. A. Offord ◽  
P. F. Meagher

Wollemia nobilis W.G.Jones, K.D.Hill D J.M.Allen isrepresented in the wild by about 40 adult trees; therefore, understanding therequirements for seed germination is important for the conservation of thismonotypic Australian conifer. Constant-temperature experiments found that seedgermination proceeded most rapidly at temperatures between 24 and 30˚C.Few seeds germinated when incubated for 112 days at 10 and 16˚C but latergerminated when transferred to 24˚C, whereas seeds initially incubated at35˚C were killed. Unstratified seeds showed a pattern of prolongedgermination taking 130 days to achieve 40% germination at 24˚C and40 days at 27˚C. Seeds stratified at 6˚C for 14 days and incubatedat 27˚C in the light achieved 40% germination within 20 days whilethose incubated at 10 and 16˚C for 112 days and transferred to 24˚Cachieved 40% germination by 15 and 24 days, respectively. Initialgermination of unstratified seeds was fastest when incubated at 30˚C inthe light, averaging 23 days. Exposure to 12-h diurnal periods of 10–15mol m–2 s–1 lightsignificantly increased 28-dayincubation germination percentages, but for onlythose incubated at 30˚C. Additions of gibberellic acid(GA3) at 1 mM had no effect on seed germination ofW. nobilis. The field observations and laboratoryexperiments indicate that following seed shed in summer and early autumn whentemperatures are high, W. nobilis seeds germinate,especially if exposed to light. The seeds that remain ungerminated or that areshed late in the season survive over winter, but germinate rapidly oncetemperatures rise in the next spring.

2020 ◽  
Vol 48 (1) ◽  
pp. 65-72
Author(s):  
Hyuk Joon Kwon ◽  
So Lim Shin ◽  
Yu-Ri Kim ◽  
Soo-Young Kim

We investigated the morphological characteristics of Maesa japonica seeds and the optimal conditions for germination. The seeds were exalbuminous, and their length and width were 0.85 ± 0.09 mm and 0.77 ± 0.05 mm, respectively. We tested germination at 15, 20, 25, 30 and 35°C; the optimum temperature for germination was 30°C (64% germination). To test the effects of gibberellic acid (GA3) and KNO3 on germination, the seeds were soaked in solutions containing 0, 0.2, 0.5, 1.0, 1.5 or 2.0 g GA3 L-1 or 0, 0.05, 0.10, 0.20 or 0.50 g KNO3 L-1 before sowing for germination. KNO3 treatment increased germination percentage and speed. Soaking in GA3 concentrations over 1.0 g L-1 stimulated 100% germination after 13 days. A presoaking treatment that combined 1.0 g GA3 L-1 and 0.2 g KNO3 L-1 promoted germination speed and shortened the time in which half of the seeds germinated. Overall, we determined that the best method for germination of Maesa japonica seeds was pre-soaking in 1.0 g GA3 L-1 and 0.2 g KNO3 L-1 at 4°C in the dark for 24 hours, followed by incubation at 25–30°C in a 16-hour light, 8-hour dark cycle for 10 days.


HortScience ◽  
2008 ◽  
Vol 43 (1) ◽  
pp. 223-228 ◽  
Author(s):  
Omar A. Lopez ◽  
Danny L. Barney ◽  
Bahman Shafii ◽  
William J. Price

Low seed germination percentages have been reported for red huckleberry (Vaccinium parvifolium Smith). Attempts to improve germination percentages and the speed of germination for red huckleberry are described. Red huckleberry seeds from two collection sites were given gibberellic acid potassium salt (GA-K) treatments (0, 500, 1000, and 1500 mg·L−1) and were germinated under three temperature regimens [constant 22 °C, 22 °C day/5 °C night (22/5 °C), and 20 °C day/13 °C night (20/13 °C) with a 12-h photoperiod]. A logistic regression model was used to assess the effects of temperature regimens and GA-K treatments on the maximum cumulative germination percentages, rates of increase, and germination lag times. For seeds untreated with GA-K, the 20/13 °C temperature regime resulted in germination percentages ranging from 30% to 61% and lag times (i.e., time to reach one-half of the maximum cumulative germination percentage) of 29 to 35 d for the two accessions. In comparison, the 22/5 °C temperature regime produced germination percentages of 12% and 38% and lag times of 38 to 64 d. The 22 °C constant temperature produced germination percentages ≤1%. Maximum germination percentages of up to 75% were obtained with 1500 mg/L GA-K. Rates of germination were generally unaffected by GA-K treatments, and germination lag times were reduced by an average of 10 d when compared with without GA-K. Improved germination percentages and reduced lag times for red huckleberry seeds were obtained by using a 20/13 °C temperature regime and 1000 to 1500 mg·L −1 GA-K.


HortScience ◽  
2000 ◽  
Vol 35 (3) ◽  
pp. 448B-448
Author(s):  
Donglin Zhang ◽  
Diemeng Hu ◽  
John Smagula

Iris versicolor (blue-flag iris) is a native aquatic plant that grows from Maine to Virginia. It is an important species of wetland regeneration and restoration. Unfortunately, seed germination seldom occurs in the wild. To address this problem, seeds of Iris versicolor were soaked with gibberellin acid (0, 500, 1000, and 1500 ppm) for 24 h after 120 days of cold treatment at 4 °C and then were randomly assigned to three germination temperatures (constant 21 °C; 24 °C/18 °C; 27C/15 °C) and placed in darkness. Germination rates for the three temperature treatments were 54.4% (21 °C), 96.5% (24 °C/18 °C), and 96.0% (27C/15 °C). Oscillating temperature treatments had significantly greater germination rate than constant temperature. Gibberellin acid had significant influence on germination rate; only the constant 21 °C was not favorable for germination. The germination rate was higher at 1000 than at 500 ppm or 1500 ppm or more. Germination occurred within 10 days under germination temperature treatments. All seedlings in petri dishes were successfully transplanted into growing flats.


Weed Science ◽  
1979 ◽  
Vol 27 (2) ◽  
pp. 146-151 ◽  
Author(s):  
R. G. Wilson

Optimum germination of Canada thistle [Cirsium arvense(L.) Scop.] occurred at alternating temperatures of 20 to 30 C and 30 to 40 C and at a constant temperature of 30 C. Osmotic pressures of 7 bars and greater reduced germination, but 2% of the seeds germinated at 15 bars. Canada thistle seeds (14%) were able to germinate in NaCl concentrations of 20,000 ppmw. Light was important in seed germination, however, its effect could be overcome by adding GA3(gibberellic acid) to the germination medium. Optimum pH for germination was between 5.8 and 7.0. Depth of planting influenced emergence; the highest percentage of seedlings emerged from depths of 0.5 to 1.5 cm. Canada thistle seedlings tolerated average soil moisture tensions of 1.3 bars and continued to grow. Canada thistle seedlings 19 days old and with two true leaves were able to resprout after top-growth removal. Regrowth was evident on 8% of the clipped plants 4 days after initial top-growth removal.


2009 ◽  
Vol 37 (1) ◽  
pp. 33-41 ◽  
Author(s):  
B. Pascual ◽  
A. San Bautista ◽  
N. Pascual Seva ◽  
R. García Molina ◽  
S. López-Galarza ◽  
...  

Botany ◽  
2019 ◽  
Vol 97 (2) ◽  
pp. 123-133 ◽  
Author(s):  
Attiat Elnaggar ◽  
Ali El-Keblawy ◽  
Kareem A. Mosa ◽  
Teresa Navarro

The effects of temperature, light, salinity, and drought on germination of halophytes have been extensively studied. However, few studies have focused on the germination of plants that grow well in both saline and nonsaline habitats (i.e., habitat-indifferent halophytes). Here, we assess the impacts of population origin, temperature, and light on drought tolerance, as simulated with polyethylene glycol (PEG), during germination of Salsola drummondii Ulbr., a habitat-indifferent halophyte from the arid Arabian deserts. Seeds were collected from both saline and nonsaline habitats and germinated at six concentrations of PEG at three temperatures and two light regimes. An increase in the concentration of PEG resulted in a significant reduction in seed germination, especially at higher temperatures. Seeds from the nonsaline habitat attained significantly greater germination efficiency at concentrations of PEG up to –1.2 MPa, but there was no difference in germination of seeds between the two habitats at concentrations of –1.5 MPa. Seeds from the saline habitat germinated significantly faster at higher concentrations of PEG. Germination was significantly higher in darkness than in light at –1.5 MPa at the lower temperatures, but the opposite was true for the higher temperatures. Seeds from saline habitats had higher levels of dormancy and faster rates of germination at higher concentrations of PEG because of their adaptation to low osmotic potentials.


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