Bibliothek

Notizen: 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.

Notizen: 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.

Notizen: Seedling emergence of Lamium amplexicaule L. and L. purpureum L. was monitored in field plots tilled at various times during the growing season, and the number of viable seeds in the soil was determined. In plots tilled in early spring, only seeds of L. amplexicaule, germinated, but seeds of both species germinated in the same plots in autumn without further disturbance. Additional seeds of L. amplexicaule, but not of L. purpureum, germinated the following spring. In plots tilled in late spring and summer, seeds of L. amplexicaule germinated in autumn and the following spring, whereas seeds of L. purpureum germinated only in autumn. The number of viable seeds in the top 13 mm layer of soil ranged from 189 to 1216 m−2 for L. amplexicaule and from 131 to 854 for L. purpureum. These field results support those obtained in previous glasshouse-laboratory physiological studies on the annual dormancy cycle in the two Lamium species. Levée au champ de Lamium amplexicaule L. et L. purpureum L. par rapport au cycle annuel de la dormance des grainesLa levée de jeunes plants de Lamium amplexicaule L. et L. purpureum L. a été observée sur des parcelles cultivées à différentes époques de la saison de végétation et le nombre de graines viables au sol a été déterminé. Sur les parcelles cultivées en début de printemps, seules les graines de L. amplexicaule ont germé, mais des graines des deux espèces ont germé en automne sur les mêmes parcelles, sans cultivation ultérieure. Au printemps suivant, une nouvelle germination a été constatée chez L. amplexicaule mais pas chez L. purpureum. Sur les parcelles cultivées en fin de printemps et en été, des graines de L. amplexicaule ont germé en automne et aussi au printemps suivant, tandis que les graines de L. purpureum n'ont germé qu'en automne. Le nombre de graines viables dans les premiers 13 mm de la surface du sol allait de 189 à 1216 m−2 pour L. amplexicaule et de 131 à 854 pour L. purpureum. Ces résultats sur le terrain confirment ceux obtenus dans des études physiologiques sur le cycle annuel de dormance chez les deux espèces de Lamium, menées préalablement en serre et au laboratoire. Ueber dus Auflaufen von Lamium amplexicaule L. und L. purpureum L. in Bezug auf den Jährlichen Zyklus der Samenruhe unter FeldbedingungenIn Parzellen, die zu verschiedenen Zeitpunkten während der Vegetationsperiode einer Boden-bearbeitung unterworfen worden waren, wurde sowohl das Auflaufen der Keimlinge von Lamium amplexicaule L. und L. purpureum L. registriert, als auch die Anzahl lebenfähiger Samen festgestellt. Nach Bodenbearbeitung im frühen Frühling keimten nur Samen von L. amplexicaule; im Herbst keimten in denselben Parzellen jedoch Samen beider Arten, sofern der Boden nicht mehr bewegt worden war. Weitere Samen von L. amplexicaule, nicht aber von L. purpureum, keimten im folgenden Frühling. In Parzellen, die im späten Frühling und im Sommer bearbeitet worden waren, keimte L. amplexicaule im Herbst und im folgenden Frühling. Während L. purpureum nur im Herbst keimte. Die Anzahl lebensfähiger Samen m−2 in den obersten 13 mm des Bodens bewegte sich zwischen 189 und 1216 für L. amplexicaule und zwischen 131 und 854 für L. purpureum. Diese Feldresultate bestätigen Ergebnisse von Gewüchshausstudien über den jährlichen Zyklus der Samenruhe der beiden Lamium-Arten.

Notizen: 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.

Notizen: 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.

Notizen: 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.

Notizen: 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.

Notizen: 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.

Notizen: 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.

Notizen: 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.