Seeds of fringed sage were collected in four different years in the Northern Mixed Prairie and placed in sealed vials in the field for up to 5 yr. The seeds were exhumed monthly and incubated at 10 or 20 C in light or darkness. Germination was greater at 10 than 20 C and greater in light than darkness. The overriding influences of light and temperature generally decreased as seeds aged. No well-defined dormancy/nondormancy or conditional dormancy/nondormancy cycles were revealed. Longevity of seeds varied among collections, ranging from 3½ to more than 5 yr. Patterns in germination of different collections were similar when they experienced the same annual changes in temperatures, indicating that germination of previously buried seeds of fringed sage was regulated by temperature. This regulating effect varied among years of storage; germination either increased or decreased with increasing temperatures, or was not affected. Results suggest that fringed sage seeds can germinate and emerge anytime during the growing season if temperature and moisture conditions are suitable. Continuous germination may enable fringed sage to occupy safe sites as they develop over time.

This study investigated the induction and loss of dormancy in oilseed rape (Brassica napus). Twenty genotypes were preliminary screened; from these, two genotypes, RGS003 and Hayola 308, which possess high potential for dormancy induction (HSD) and medium potential to induce secondary dormancy (MSD), were selected. The stratification of seeds at alternating temperatures of 5–30°C (in dark) significantly relieved secondary dormancy, but dormancy was not fully released. The ψb(50) values were −1.05 and −1.06 MPa for the MSD and the HSD before dormancy induction. After inducing dormancy, the ψb(50) values for the MSD and the HSD were increased to −0.59 and −0.01 on day 0 stratification at 20°C. The hydrothermal time (θHT) value was low for one-day stratification for HSD in comparison with other stratification treatments. Water stress can induce dormancy (if the seeds have the genetic potential for secondary dormancy) and warm stratification (in dark) can only reduce the intensity of dormancy. The seeds with a high potential of dormancy induction can overcome dormancy at alternating temperatures and in the presence of light. It can, therefore, be concluded that a portion of seeds can enter the cycle of dormancy ↔ non-dormancy. The secondary dormant seeds of B. napus cannot become non-dormant in darkness, but the level of dormancy may change from maximum (after water stress) to minimum (after warm stratification). It seems that the dormancy imposed by the conditions of deep burial (darkness in combination with water stress and more constant temperatures) might be more important to seed persistence than secondary dormancy induction and release. The dormancy cycle is an important pre-requisite in order to sense the depth of burial and the best time for seed germination.

Pretreatment of moist seeds at certain temperatures can reduce seed dormancy, but such observations represent the net effect of pretreatment. Seeds of Sitka spruce (Picea sitchensis [Bong.] Carr.) were raised to 30% moisture content and pretreated at five different temperatures between 5 and 30°C for up to 24 weeks (168 d). Subsequent ability to germinate at 10°C and viability were then determined in order to investigate the effects of pretreatment on seed dormancy and survival. There was a curvilinear, negative semi-logarithmic relationship between seed longevity and pretreatment temperature, such that Q10 for loss in viability increased from 2.6 between 10 and 20°C to 2.8 between 20 and 30°C. Simple multiplicative models combining cumulative normal frequency distributions for each of loss in viability and loss in dormancy were able to describe the changes in ability to germinate at 10°C, after pretreatment at 5, 10 and 30°C. However, in order to quantify the changes in ability to germinate observed at 10°C after pretreatment at 15°C, it was necessary also to invoke a model of dormancy reimposition, while for the results at 20°C it was necessary to postulate both dormancy reimposition and the further loss of this reimposed dormancy. It is concluded that moist seeds of Sitka spruce held at 15 and 20°C cycle between the dormant and non-dormant condition.

Prechilling seeds of Sitka spruce (Picea sitchensis [Bong.] Carr.) at 4°C with 30% moisture content for 12–14 weeks (84–98 d) removed conditional dormancy (i.e. they were then able to germinate at 10°C). The non-dormant status was preserved after redrying to 6% moisture content. However, conditional dormancy was gradually reimposed during subsequent air-dry storage at 4°C and 6% seed moisture content in all five seed lots tested. Further investigations with one seed lot showed that reimposition was reversed by a second prechill treatment, but was reimposed again during subsequent air-dry storage. The trend of dormancy reimposition within seed lots over time was quantified by negative exponential relations between ability to germinate at 10°C and duration of air-dry storage. The progress of dormancy reimposition was influenced by seed storage moisture content and was most rapid at 4–10%. At higher moisture contents (15 and 20%) the rate of the reimposition of conditional dormancy was much reduced, while at moisture contents of 25 and 30% further loss in dormancy occurred. Thus it is clear that dormancy reimposition occurred during storage at low water potential rather than solely during desiccation from high to low water potential.