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1.
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
2.
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
3.
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
4.
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
5.
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
6.
Temperature requirements for after-ripening were investigated in seeds of the weedy winter annuals Arabidopsis thaliana, Arenaria serpyllifolia, Capsella bursar-pastoris, Cardamine hirsuta. Cerastium viscosum, Draba verna, Holosteum umbellatum, Stellaria media and Thlaspi per-foliata. Fresh seeds of seven species were innately dormant, and those of A. serpyllifolia and C. viscosum were conditionally dormant. (Dormancy terminology follows Vegis, 1964.) Seeds of each species were buried in moist soil at 5, 15/6, 20/10, 25/15, 30/15 and 35/20°C from time of maturation in spring until the third week of September. Buried seeds at each temperature were then exhumed and tested in light at all six temperatures. Seeds of all species became non-dormant at 25/15, 30/15 and 35/20°C, except for those of D. verna, H. umbellatum, A. serpyllifolia and C. viscosum, which rotted during burial at 35/20°C At 20/10°C. seeds of T perfoliata and D. verna became conditionally dormant, and those of the other seven species became non-dormant. Thalaspi perfoliata and D. verna seeds did not after-ripen at 5 or 15/6°C, while those of H. umbellatum and C. hirsuta became conditionally dormant at 15/6°C but remained innately dormant at 5°C. The other five species became conditionally dormant at both 5 and 15/6°C; they germinated at low, bill not at high, temperatures. Thus, after-ripening in seeds of winter annuals is fully promoted by high summer temperatures and wholly or partially inhibited by low winter temperatures. Exigences en temperature pour la post-maturation des semences de neuf espèces annuelles d'hiver Les exigences en température pour la post-maturation ont étéétudiées chez les semences d'adventices annuelles d'hiver, Arabidopsis thaliana, Arenaria serpyllifolia, Cupsella bursa-pastoris, Cardamine hirsuta, Cerastium viscosum, Draba verna, Holosteum umbellatum, Stellaria media et thlaspi perfaliata. Les semences fraîches de sept espèces manifestaient une dormance absolue, et celles de A. serpyllifolia et C. viscosum une dormance relative (selon la terminologie de Vegis, 1964). Des semences de chaque espèce ont été enfouies dans du sol humide à 5, 15/6, 20/10, 25/15, 30/15 et 35/20°C, à partir de la période de maturation au printemps et jusqu'à la troisième semaine de Septembre. Les semences enfouies aux différentes températures ont été ensuite exhumées et soumise, sous éclairement, aux six conditions de température. Les semences de toutes les espèces ont perdu leur dormance à 25/15, 30/15 et 3/20°C, excepté celles de D. verna. H. umbellatum, A. serpillyfolia et C. viscosum, qui ont pourri après a voir été enfouies à 35/20°C. A 20/10°C, les semences de. T. perfoliata et D. verna ont acquis une dormance relative et celles des sept autres espèces sont devenues non dormantes Les semences de Thlaspi perfoliata et D. verna n'ont pas subi de post-maturation à 5 ou 15/6°C, alors que celles de H. umbellatum et de C. hirsuta ont acquis une dormance relative à 15/6°C mais ont conserveé une dormance absolue à 5°C. Les cinq autres espèces ont acquis une dormance conditionnelle à la fois à 5 et 15/6°C; elles ont germéà basse, mais non à haute température. Par consèquent, la post-maturation des semences d'annuelles d'hiver est totalement induite par les fortes tempéeratures d'été, et totalement ou partiellement inhibée par les basses températures d'hiver. Temperaturhedürftnisse zur Nachreifung von Samen bei neun Winterannuellen In dieser Studie wurden die Temperaturanor- derungen zur Nachreifung der Samen der winter-annuellen Unkräuter Arabidopsis thaliana, Arenaria serpyllifolia, Capsella bursa-pastoris, Cardamine hirsuta, Cerasthim viscosum, Draba verna, Holosteum umbellatum, Stellaria media und Thlaspi perfoliata untersucht. Junge Samen von sieben Arten sind von Natur aus obligat und diejenigen von A. serpyllifolia und C. viscosum je nach Umständen dormant (Terminologie der Samenruhe nach Vegis, 1964). Samen jeder Species wurden zur Zeit der Samenreife im Frühling in feuchtem Boden eingegraben und darin bei Temperaturen von 5, 15/6, 20/10, 25/15, 30/15 und 35/20°C bis zur dritten Woche im September belassen. Danach wurden die Samen ausgegraben und unter Lichleninfluss bei allen sechs Temperaturstufen auf ihre Keimfähigkeit getestet. Mit Ausnahme der Samen von D. Verna, H. umbellatum, A. serpyllifolia und C. viscosum, welche bei 35/20°C im Boden verfault waren, wurden alle anderen Arten bei 25/15, 30/15 und 35/20°C keimfähig. Bei 20/10 °C kamen die Samen von T. perfoliata und D. verna in einen bedingten Ruhezustand, während diejenigen der anderen sieben Arten voll keimfähig wurden. T. perfoliata und D. verna reiften bei 5 oder 15/6°C nicht nach: H. umbellatum und C. hirsuta wurden bei 15/6 °C bedingt keimfähig, blieben aber bei 5°C völlig dormant. Die anderen fünf Arten erreichten bei 5 und 15/6°C eine bedingte Dormanz; sie keimten bei niedrigen, nicht aber bei hohen Temperaturen. Aus diesen Ergenissen lässt sich schlicssen, dass die Nachreifung von Samen winterannueller Arien durch hohe Sommertemperaturen voll entwickelt, durch niedrige Wintertemperaturen aber ganz oder teilweise gehemmt wird. 相似文献
7.
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
8.
Buried seeds of Capsella bursa-pastoris exhibit an annual conditional dormancy/non-dormancy cycle. Seeds after-ripen during summer and remain non-dormant during autumn and winter. Seeds enter conditional dormancy in early spring, first showing marked decreases in ability to germinate at high (35/20°C) and then at lower (30/15, 25/15°C) temperatures. Seeds do not lose the ability to germinate to high percentages at March (15/6°C) and April (20/10°C) temperatures in March and April. Thus, C. bursa-pastoris is a facultative winter annual, germinating in both autumn and spring if seeds are exposed to light. However, because some seeds retain the ability to germinate at 30/15 and 25/15°C, they could do so throughout the growing season in regions with cool, moist summers. Conditional dormancy developed in all seeds given 12 weeks at 5°C and subsequently kept for 4 weeks each at March (15/6°C), April (20/10°C) and May (25/15°C) temperatures. Thus, seeds of C. bursa-pastoris enter conditional dormancy as temperatures increase in spring. 相似文献
9.
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
10.
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
11.
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
12.
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
13.
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
14.
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
15.
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
16.
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
17.
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
18.
Emergence of Veronica hederifolia seedlings began in mid-October and continued into spring; few appeared from June to September. Ripe seeds shed in June were dormant but wben buried in soil outdoors developed a capacity for germination initially at low temperatures (constant4 C; daily alternations of 4-10° and 4-1 5 C) and later at somewhat higher temperatures, with peak germination in September-November. During winter, spring and early summer thc germination capacity declined, to increase again in late summer and early autumn. Cyclic physiological changes thus occur in seeds of V,hederifolia present in the soil, with which lhe consistent seasonal periodicity of seedling emergence is associated. In dry storage ihe capacity for germination progressively increased, but alter 12 months there was a sharp decline in germination at 4° C. Few seeds germinated at 20° C, but moistening with GA 4/7; brought about complete germination at this temperature. 相似文献
19.
The effect of temperature on the germination response of two categories of morphologically different seeds of Cassia tora L. was investigated. Germination response of dormant seeds (category A with closed ultraastructures) was not affected by temperature, as 96% of the seeds germinated at all temperatures on scarification. On the other hand, non-dormant seeds (category B with open ultrastructures) were temperature sensitive and germinated best at 32°C. However, storage affected the germination responses of both types. While the category A seeds lost moisture gradually with storage time and retained viability for a longer period, i.e. 2 years, the moisture loss in category B seeds was noted only after 2 years and the seed viability was retained for only 1 year. The production of two morphologically and physiologically distinct types of seed simultaneously by C. tora is probably an ecological adaptation for progressive emergence of the species over long periods in the field. 相似文献
20.
Hengzhi Wang Kongping Zhao Xiangju Li Xiutao Chen Weitang Liu Jinxin Wang 《Weed Research》2020,60(3):171-181
Information on seed germination and emergence ecology of Aegilops tauschii is scant, despite it being a widespread invasive weed in China. We conducted this study to determine the effects of various factors on seed germination and seedling emergence in three A. tauschii populations. Seeds germinated across a wide range of temperatures (5–35°C), with germination of over 90% at 15–20°C. Germination was completely inhibited when dry seeds were exposed to a temperature of 160°C for 5 min; a similar response was observed for pre-soaked seeds at 100°C. Light was neither required for nor inhibited germination. Germination was not significantly affected by pH. Aegilops tauschii was relatively tolerant to low osmotic potential and high salt stress: over 80% of seeds germinated at −0.3 MPa, and all three populations germinated in the presence of 400 mM salt (NaCl) although salt tolerance varied among the populations. Seeds buried at depths of 1–3 cm emerged well, but emergence was completely inhibited at depths greater than 8 cm. The addition of maize straw caused a linear reduction in seedling emergence, although the rate of reduction varied among the populations. The results of this study have contributed to understanding the requirements of A. tauschii germination and emergence and optimising an integrated management system for this weed in Huang–Huai–Hai Plain of China. In addition, our study provides data for development of models to predict the geographical distribution of this weed. 相似文献