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1.
The annual dormancy cycle was investigated in buried seeds of Polygonum aviculare L. exposed to natural temperature changes in Lexington, Kentucky, U.S.A. Seeds were exhumed monthly from December 1984 to February 1987 and tested in light (14-h daily photoperiod) and continuous darkness at 12/12-h daily alternating temperature regimes of 15/6, 20/10, 25/15, 30/15 and 35/20°C. During autumn and winter, seeds became non-dormant, and in March 1985 they germinated to 95-100% at all thermoperiods in light and to 7-61% in darkness. Seeds remained non-dormant during spring but became more specific in their germination requirements in early summer. During July and August 1985, seeds germinated to 17-53% in light at 30/15 and 35/20°C but to 0-10% at all other test conditions. By September, about 65% of the seeds were dormant, but the others were able to germinate under the higher alternating temperatures in light. A similar seasonal cycle was recorded in the following year through to the spring of 1987. The results confirm the seasonal pattern of dormancy in this species (Courtney, 1968) but indicate that alternating temperatures combined with light are important in determining germination potential in P. aviculare. 相似文献
2.
Summary. Most freshly-matured seeds of Thlaspi arvense L. (Brassicaceae) were dormant at maturity in May. Seeds sown on soil germinated in autumn and spring, but mostly in autumn. Buried seeds exhumed at monthly intervals and tested in light and darkness over a range of thermoperiods exhibited annual dormancy/non-dormancy cycles. However, the dormant period was short, usually only in April, but sometimes May, and in some years 1–6% of the seeds remained conditionally dormant. After-ripening occurred during summer, and seeds were non-dormant during autumn. Seeds entered conditional dormancy in winter and dormancy in late winter or early spring. When buried dormant seeds were kept at 25/15, 30/15 or 35/20°C for 12 weeks, they gained the ability to germinate to 95–100% at 15/6, 20/10, 25/15, 30/15 and 35/20°C. After burial for 12 weeks at 15/6 and 20/10°C, seeds germinated to 80–100% at 15/6, 20/10 and 25/15°C. but to only 11–64% at 30/15 and 35/20°C. After 4 weeks at 5°C, initially-dormant seeds germinated to 100% at all thermoperiods except 35/20°C, where only 15% of them germinated. However, after 18 weeks at 5°C, only 0–1% of the seeds germinated at all thermoperiods. Most non-dormant seeds exposed to 1, 5 and 15/6°C for 16 weeks were induced into dormancy; 1–15% entered conditional dormancy and thus germinated only at 15/6, 20/10 and 25/15°C. This study indicates that seeds of winter annual plants of T. arvense are non-dormant in autumn and enter dormancy in winter, while those from summer annuals are dormant in autumn and become non-dormant during winter. 相似文献
3.
Low temperatures may inhibit dormancy break in seeds of winter annuals, therefore it was hypothesized that seeds of Capsella bursa‐pastoris and Descurainia sophia that mature at high latitudes in late summer–early autumn would not germinate until they had been exposed to high summer temperatures. Consequently, germination would be delayed until the second autumn. Most freshly matured seeds of both species collected in August and September in southern Sweden were dormant. After 3 weeks of burial at simulated August (20/10°C) and September (15/6°C) temperatures, 28 and 27%, respectively, of the C. bursa‐pastoris and 56 and 59%, respectively, of the D. sophia seeds germinated in light at 15/6°C. In contrast, in germination phenology studies conducted in Sweden, only a few seeds of either species germinated during the first autumn following dispersal. However, there was a peak of germination of both species the following spring, demonstrating that dormancy was lost during exposure to the low habitat temperatures between late summer and early autumn and spring. Nearly 100% of the seeds of both species subjected to simulated annual seasonal temperature changes were viable after 30.5 months of burial. In the burial study, exhumed seeds of C. bursa‐pastoris were capable of germinating to 98–100% in light at the simulated spring–autumn temperature regime (15/6°C) in both spring and autumn, while those of D. sophia did so only in autumn. In early spring, however, seeds of D. sophia germinated to 17–50% at 15/6°C. Thus, most seeds of these two annual weeds that mature in late summer do not germinate in the first autumn, but they may do so the following spring or in some subsequent autumn or spring. 相似文献
4.
Spring-produced seeds of Lamium amplexicaule L. were buried in pots of soil in an unheated glasshouse in June 1978, and at 1–2-month intervals, for 27 months, they were exhumed and tested for germination in light and darkness at temperatures simulating those in the habitat from early spring to late autumn. Freshly-matured seeds were dormant, but by autumn 85% or more germinated in light at 15/6, 20/10, 25/15 and 30/15°C but only 7% or less in darkness. During late autumn and winter germination in light decreased at 25/15 and 30/15 °C but not at 15/6 and 20/10 °C, and germination in darkness increased at 15/6 and 20/10 °C. During late winter and early spring germination in light at 15/6 and 20/10 °C decreased, and seeds lost the ability to germinate in darkness. By the second autumn of burial, seeds germinated to near 100% in light at 15/6 to 30/15 °C and to 10–25% in darkness at 15/6 and 20/10 °C. The cycle of germination responses was repeated during the second winter and spring and the third summer of burial. Autumn-produced seeds were dormant when buried in November 1979, but by spring they germinated to 81 and 36% at 15/6 and 20/10 °C, respectively, in light. These seeds afterripened further during summer. The consequence of seasonal changes in germination responses is that (1) seeds can germinate in the habitat in late summer, autumn and spring but not in early- to mid-summer or in late autumn and winter and (2) during both germination seasons, seeds produced during the previous spring(s) and/or autumn(s) can germinate. 相似文献
5.
Freshly matured, seeds of the four summer annuals Ambrosia artemisiifolia, Polygonum pensylvanicum, Amaranthus hybridus and Chenopodium album were buried in soil at (12/12 h) daily thermoperiods of 15/6, 20/10, 25/15, 30/15 and 35/20°C and at a constant temperature of 5°C. After 0, 1, 3 and 5 months, seeds of each species at each temperature were exhumed and tested at a 14-h daily photoperiod at all six temperatures. Fresh seeds of A. artemisiifolia and P. pensylvanicum did not germinate at any temperature, those of A, hybridus germinated to 4 and 64% at 30/15 and 35/20°C, respectively, and those of C. album to 11–20% at 25/15, 30/15 and 35/20°C. Seeds of A. artemisiifolia and P. pensylvanicum, which germinate only in spring, required exposure to low (5, 15/6°C) temperature to after-ripen completely (i.e., to gain the ability to germinate over a wide range of temperatures), and little or no after-ripening occurred at high (25/15, 30/15 and 35/20°C) temperatures. Seeds of A. hybridus and C. album, which germinate in spring and summer, required exposure to low temperature to after-ripen completely, but at high temperatures they rapidly gained the ability to germinate at high temperatures. Regardless of the burial temperatures and species, when after-ripening occurred, seeds firs germinated at high and then at low temperatures. The minimum germination temperature for a species decreased with after-ripening temperature and with an increase in the length of the burial period. 相似文献
6.
Seeds of Setaria glauca (L.) Beauv. buried in soil and exposed to natural temperature cycles exhibited seasonal changes in temperature, but generally not light; dark requirements for germination. Seeds were dormant at maturity in late September and October (autumn), and during burial from October to January they entered conditional dormancy, germinating up to ≥60% in light and darkness at daily thermoperiods of 25/15,30/15 and 35/20^C by January. During burial from February to May or June, seeds became non-dormant and germinated up to 68–100% in light and darkness at 15/6,20/10,25/15,30/15 and 35/20^C in May or June. At maximum yearly temperatures in June or July–August, 65–89% of the seeds entered conditional dormancy (germinating at 30/15 and 35/20, but not at 15/6,20/10 and 25/15^C), and the others entered dormancy (not germinating at any thermoperiod). Thus, most buried seeds had an annual conditional dormancy/non-dormancy cycle, but some had an annual dormancy/non-dormancy cycle. Except for seeds buried in 1990 that lost the ability to germinate in darkness at all thermoperiods the first summer of burial, seeds incubated in light and in darkness exhibited the same patterns of seasonal changes in germination responses. Although conditionally dormant and non-dormant seeds germinated to high percentages in darkness in Petri dishes, seedlings were found only in bags of seeds exhumed in April and May 1983, indicating that some factor(s) associated with the burial environment other than darkness prevented germination of buried seeds. 相似文献
7.
Seeds of Viola arvensis collected in different years and in different months within those years were buried in soil under natural seasonal temperature cycles, and changes in their germination requirements monitored. Seeds were dormant at maturity in May or June, but nondormant by autumn. During winter, some seeds entered dormancy, while others entered conditional dormancy, i.e. retained the ability to germinate at 15/6 and 20/10oC but not at other thermoperiods. Dormant and conditionally dormant seeds became nondormant the following summer. Seeds collected in 1981 exhibited an annual dormancy:nondormancy cycle, while those collected in 1982 exhibited an annual conditional dormancy:nondormancy cycle. The type of dormancy cycle found in these seed lots during their first year of burial persisted in subsequent years. Thirty–five and 36% of seeds collected in May 1983 and 1986, respectively, were conditionally dormant the following May, while only 5 and 9% of those collected in the same field in June 1983 and 1986, respectively, were conditionally dormant. Dormant seeds collected in 1981,1982 and 1984 and buried at 5oC during summer germinated to 0, 33 and 0% respectively, at 15/6oC in autumn. After the 1982 seeds became nondormant during summer, only 25% entered conditional dormancy when buried at 5oC, but after the 1981 and 1984 seeds became nondormant, 100% entered conditional dormancy at 5oC. Thus, the persistent seed bank of V. arvensis at a population site may consist of seeds with an annual dormancy:mondormancy cycle and others with an annual conditional dormancy:nondormancy cycle. This is the first report of the two types of annual seed dormancy cycles in the same species. 相似文献
8.
Embryos in freshly matured seeds of the facultative winter annual Papaver rhoeas are underdeveloped and physiologically dormant; thus, seeds have morphophysiological dormancy (MPD). Seeds lost physiological dormancy during 12 weeks of burial in moist soil at 12 h/12 h daily alternating temperature regimes of 15/5°C, 20/10 °C and 25/15 °C but not at 1 °C. Physiological dormancy was not broken in seeds stored dry at room temperature for 12 weeks. After physiological dormancy was broken, seeds required light for embryo growth (i.e. for loss of morphological dormancy) and consequently for germination. After a 12-week period of burial in soil at 25/15 °C, seeds that matured in 1997 germinated to 100% in light at 25/15 °C, demonstrating that cold stragification temperatures (≈ 0.5–10 °C) are not required for embryo growth. Thus, seeds have non-deep simple MPD. During exposure to low winter temperatures (5/1 °C, 1 °C), 52% of the seeds with physiologically non-dormant embryos entered conditional dormancy and thus lost the ability to germinate at 25/15 °C but not at 15/5 °C or 20/10 °C. The peak of germination for seeds sown in southern Sweden was in autumn, but some also germinated in spring. A higher percentage of seeds that matured in a relatively warm, dry year (1997) came out of MPD and germinated than did those that matured in a relatively cool, wet year (1998) at the same site. 相似文献
9.
Spring-produced seeds of Lamium amplexicaule L. were dormant at maturity in May and after-ripened when buried and stored over a range of temperatures, becoming conditionally dormant at low (5, 15/6 and 20/10°C) and non-dormant at high (25/15, 30/15 and 35/20°C) temperatures. Conditionally dormant seeds germinated to high percentages at 5 and 15/6°C, and non-dormant seeds germinated to high percentages at 5, 15/6, 20/10, 25/15 and 30/15°C. Seeds that became conditionally dormant at 5°C afterripened completely (i.e. became non-dormant) after transfer to 30/15°C. Buried seeds that became non-dormant in a non-temperature-controlled glasshouse during summer were still non-dormant after 12 weeks of storage at 30/15°C, while those stored at 5°C for 12 weeks had entered conditional dormancy. Thus, low temperatures cause reversal of the afterripening that takes place at high temperatures, but not that which takes place both at low and at high temperatures. Low winter temperatures cause dormant autumn-produced seeds and non-dormant seeds in the soil seed pool to become conditionally dormant. The ecological consequences of these responses to temperature are discussed in relation to the timing of seed germination in nature. 相似文献
10.
Physiological dormancy in weed species has significant implications for weed management, as viable seeds may persist in soil seedbanks for many years. The major stimulatory compound in smoke, karrikinolide (KAR1), promotes germination in a range of physiologically dormant weed species allowing targeted eradication methods to be employed. Control of Chrysanthemoides monilifera ssp. monilifera (boneseed), a Weed of National Significance in Australia, may benefit from adopting such an approach. In this study, we hypothesised that seeds of C. monilifera ssp. monilifera exhibit physiological dormancy, germinate more rapidly as dormancy is alleviated, show fluctuations in sensitivity to KAR1 and form a persistent soil seedbank. Seeds responded to 1 μM KAR1 (40–60% germination) even during months (i.e. March, April, July, August) when seeds were observed to be more deeply dormant (control germination: 7–20%). Seeds germinated readily over a range of cooler temperatures (i.e. 10, 15, 20, 20/10 and 25/15°C) and were responsive to KAR2 (~50% germination) as well. Eradication efforts for C. monilifera ssp. monilifera may benefit from use of karrikins to achieve synchronised germination from soil seedbanks, even at times of the year when C. monilifera ssp. monilifera seeds would be less likely to germinate, allowing more rapid depletion of the soil seedbank and targeted control of young plants. 相似文献
11.
Role of temperature in regulating timing of germination in soil seed reserves of Lamium purpureum L.
Fresh seeds of Lamium purpureum L. were dormant at maturity, and when buried and exposed to natural seasonal temperature changes they exhibited an annual dormancy/non-dormancy cycle. During burial in summer, fresh seeds and those that had been buried for 1 year afterripened and thus were non-dormant by September and October; light was required for germination. During autumn and winter seeds re-entered dormancy, and during the following summer they became non-dormant again. Dormant seeds afterripened when buried and stored over a range of temperatures, becoming conditionally dormant at low (5, 15/6°C) and non-dormant at high (20/10, 25/15, 30/15 and 35/20°C) temperatures. Conditionally dormant seeds germinated to high percentages at 5, 15/6 and 20/10°C, while non-dormant seeds germinated to high percentages additionally at 25/15, 30/15 and 35/20°C. Low temperatures caused non-dormant seeds to re-enter dormancy, while high temperatures caused a sharp decline in germination only at 30/15 and 5°C. The temperature responses of L. purpureum seeds are compared to those of L. amplexicaule L. 相似文献
12.
Freshly harvested seeds of Poa annua L. collected in south Louisiana were stored in moist soil at seven temperatures between 5°C and 35°C. At monthly intervals, seed lots were removed and germinated at each of the seven temperatures. Seed were dormant for at least 1 month at all test temperatures. Seeds stored for 2 months at 30 and 35°C showed conditional dormancy; there was 100% germination at 10 or 15°C, and poorer germination at 5 or 20°C. Seeds started to lose viability after 2 months at 35°C and were dead after 7 months. In seeds stored at 10–30°C, there were increased percentages and a wider range of germination temperatures as storage time or storage temperatures increased. Seeds stored at 10°C remained dormant for 9 months, but by 12 months of storage the seeds germinated only at 5 or 10°C. Nearly all seeds stored at the same temperatures in air dry soil remained dormant for 6 months, regardless of storage temperature. These results differ from other reports of low temperatures breaking seed dormancy in Poa annua L. and suggest an adaptation to subtropical climates. 相似文献
13.
Seeds of Poa annua from original collections in Louisiana, Maryland and Wisconsin were grown together in Louisiana over a 3-year period. The freshly harvested seeds and samples stored in moist soil at 30°C were tested for germination at a range of temperatures to compare dormancy and germination characteristics. Seeds of the Louisiana population were dormant over the germination temperature range of 5–25°C, and imbibed storage for 2 weeks did not break dormancy. Freshly harvested seeds of the Maryland population germinated well (78%) at 10°C. With 1 week of imbibed storage at 30°C, germination was good over the range from 5 to 15°C and near 50% at 20°C. Storage for 2 weeks had little further effect. Freshly harvested seeds of two Wisconsin populations germinated above 50% throughout the range of temperatures, and imbibed storage for 2 weeks at 30°C had no effect on germination. The variations in the dormancy of freshly harvested seeds and the varying responses of dormancy breaking from storing imbibed seeds at 30°C suggests that these populations have adapted to avoid high summer temperatures in Louisiana and Maryland but to grow as a summer annual in Wisconsin. 相似文献
14.
Thlaspi perfoliatum L. is an introduced winter annual that grows in waste places, but it is not a troublesome agricultural weed. Seeds are dormant at maturity in spring, afterripen during summer and germinate in autumn. Non-dormant seeds that fail to germinate in autumn are induced into secondary dormancy by low winter temperatures and cannot germinate the following spring. These seeds afterripen during summer and germinate in autumn if conditions are suitable. Vernalization is not an absolute requirement for flowering. However, it shortens the time to flowering, and vernalized plants produce many more flowers and seeds than non-vernalized plants. Results from studies on seed germination and flowering of T. perfoliatum are compared to published studies on the life cycle of Thlaspi arvense L., an introduced species that is a serious agricultural weed which behaves both as a winter and a summer annual. 相似文献
15.
Freshly-collected mature mericarps of Aethusu cynapium were dormant, but some germinated at alternating (16 h low/8 high) temperatures when the seed coverings were removed. Burial during winter increased percentage germination and the temperature range over which it took place. In late spring the range narrowed, first at low and then at higher temperatures, widening again in autumn. Moist storage at both low (4°C) and high (30°C) temperatures overcame dormancy, but exposure to 30°C inhibited subsequent germination at low temperatures. Germination of intact mericarps was consistently lower than that of de-coated seeds. The cyclic change in dormancy status of the seeds appears to interact with the restricting effects of the seed coverings and perhaps other factors in determining the consistent pattern of spring emergence in A. cynapium. 相似文献
16.
Summary Heteranthera limosa seeds were buried in flooded and in non-flooded soil and exposed to natural seasonal temperature changes in Lexington, Kentucky, USA. Seeds exhumed after various periods of burial ranging from 2 to 36 months were tested for germination under both flooded and non-flooded conditions. Seeds were dormant at maturity in September and became non-dormant during winter. Seeds buried in non-flooded soil during winter germinated to higher percentages and over a wider range of temperatures when tested under flooded conditions (in light) during spring and summer, than did those buried in flooded soil during winter. Thus, the water regime associated with rice culture (non-flooded in winter and flooded in summer) is optimal for dormancy-break and germination of H. limosa seeds. A portion of the buried seeds exhibited an annual dormancy/non-dormancy cycle, whereas others had a conditional dormancy/non-dormancy cycle. Regardless of the type of cycle, seeds buried in non-flooded soil retained the ability to germinate in light at high temperatures under flooded conditions throughout the summer. Thus, seeds potentially can germinate at any time during the growing season, whenever rice fields are flooded. Flooding fields during winter and/or sowing rice relatively early in the growing season may help in establishing rice before seeds of H. limosa germinate. 相似文献
17.
Field emergence and temperature requirements for germination in Solanum sarrachoides Sendt. 总被引：1，自引：1，他引：0
Emergence of Solanum sarrachoides began in late April, reached a peak in May or June and ceased in September. This pattern closely resembled that for S. nigrum L., whereas almost all seedlings of S. dulcamara L. emerged in April. Fresh seeds of S. sarrachoides were dormant but developed a capacity for germination at 25 and 30°C and at alternating (16 h low/8 h high) temperatures of 4/25, 10/25, 10/30 and 20/30°C when stored dry. kept moist at 4°C or buried in the field. Buried seeds also became capable of germinating at 10. 15 and 20°C and the temperature range for germination was widest during April-June. Induced dormancy developed during August and the range narrowed. The consistent seasonal emergence pattern appears to be associated with cyclic changes in the dormancy status of buried seeds. 相似文献
18.
The dormancy of wild oat seed (Avena fatua L.) from plants grown under various temperature and soil moisture conditions 总被引：1，自引：0，他引：1
N. C. B. PETERS 《Weed Research》1982,22(4):205-212
Wild oat plants of types fA, fB and fC were grown at a constant 15 or 20°C during the period of seed maturation. Seed of the three types differed little in dormancy when grown at 15°C, but at 20°C a larger proportion of seeds of type fA were dormant compared with fB or fC. Overall, dormancy of seed produced at 15 and 20°C was 97 and 63% respectively. Plants of another collection of type fB were grown from seed at 15 or 20°C with or without water stress applied only from the time of panicle emergence. Water stress and high temperature reduced viable seed production. Seed dormancy was tested immediately after collection by planting the seed in soil, and by Petri dish tests. Further Petri dish tests were made after 6 months storage. Seedling emergence in the first autumn from seeds of plants matured without water stress at 15°C was 10% compared with 30% for seeds grown at 20°C. Seeds grown with water stress at 15°C gave 47%, and at 20°C 78% emergence. The majority of emergence from seeds formed at 15°C without water stress occurred in the second spring after burial. Petri dish tests support these findings and suggest that seeds produced in hot dry summers are less dormant than those produced in cool moist ones. 相似文献
19.
Seeds of Poa trivialis L. were collected from one grassland and two arable habitats. Seeds from the grassland population were less dormant than the arable populations. Distal (upper) seeds were consistently more dormant than proximal (basal) seeds. Dry storage at 4°C and 15°C for 4 weeks after shedding resulted in a slightly greater loss of dormancy than storage at 23°C. Germination was enhanced by subjecting seeds stored at 15°C to repeated hydration and dehydration cycles. Germination of P. trivialis seeds was density-dependent. Germination of distal seeds was particularly impaired at high densities. The ecological implications of these results are discussed in relation to seed survival strategies. 相似文献
20.
Study of seasonal variation in dormancy of Spergula arvensis L. seeds in a condensed annual temperature cycle 总被引：3，自引：0，他引：3
Changes in dormancy of Spergula arvensis seeds were studied during pre-incubation at constant temperatures and under a temperature regime that condensed the annual temperature cycle into 73 days. Each day in the regime represented the mean day and night temperatures and day lengths of 5 successive days of an average year in The Netherlands. Incubation occurred in water or loamy sand, in darkness. Germination of the seeds was tested in water or KNO3 over a range of temperature. Seeds were irradiated with saturating doses of red light. In half of the treatments, pre-incubated seeds were dehydrated at the transfer to the conditions of the germination test. Breaking of dormancy occurred under conditions of 'spring'. It did not depend on exposure to low‘winter’temperatures, but was induced by rising 'spring’temperatures. Seeds developed secondary dormancy in late‘autumn'. The expression of the changes in dormancy that were induced during pre-incubation depended on the conditions of the germination test. Light, nitrate and dehydration stimulated germination. The experiments predicted that field emergence from nitrate-poor soils that have not been dehydrated will be restricted to a short period in autumn, whereas disturbance of nitrate-rich soils followed by a dry spell will stimulate germination of S. arvensis seeds from early spring to late autumn. The data presented good explanations for the cosmopolitan character and the serious weediness of this species. Its classification as a summer or winter annual is discussed. 相似文献