Germination of seeds of some summer annuals in Kentucky (eastern USA) in late-winter lead to the hypothesis that under present climate conditions the whole length of the winter cold stratification (CS) period is not required for dormancy-break of seeds of summer annuals with physiological dormancy (PD). We evaluated our data from germination phenology studies of 45 species (69 datasets) and buried-seed studies of 33 species (44 datasets). We determined time and temperature of germination after CS and percentage of the total number of hours of CS during winter (% of winter CS) seeds received prior to start of germination. In the phenology studies, mean temperature during the week of first germination for C3 and C4 species was 11.1 and 14.4°C, respectively, and % of winter CS was 80.8 and 87.4, respectively. In the buried-seed studies, % of CS for C3 and C4 species was 40.8 and 48.1, respectively, when they germinated to 25% at 20/10°C. For 32 of 33 species in the buried-seed studies, the minimum temperature at which seeds germinated decreased with increased CS; thus, seeds had Type 2 non-deep PD. The time of germination is controlled by a number of hours of CS, a decrease in minimum temperature at which seeds can germinate and a temperature increase in early spring. Seeds can germinate at relatively high temperatures as early as December and January, but they continue to be CS until spring. Temperature increases in eastern North America due to global warming are not likely to inhibit the germination of summer annuals with PD in spring.

Weed seed and seedling populations, and weed competition were compared in plots of continuous corn and corn/soybean rotation under ridge and conventional tillage. After 7 to 8 yr of standard chemical and mechanical weed control, from 1500 to 3000 weed seeds/m2 (to a 10-cm depth) were found in continuous corn with ridge tillage whereas about two-thirds fewer seeds were found in conventionally tilled corn. Soil from a corn/soybean rotation had from 200 to 700 seeds/m2 in both tillage systems. Annual loss of weed seeds from the soil through germination was from 3 to 12% in ridge tillage and 11 to 43% in conventional tillage. Additions to the seed pool were supplied by small weeds whose germination was stimulated by “layby” cultivation, with up to 10 times more emergence and 140 times more seed production in ridge than in conventional tillage. Withholding herbicides for 1 yr reduced yields of continuous corn by 10 to 27% in ridge tillage, only 2 to 4% in conventional tillage, and negligibly in corn/soybean rotations regardless of tillage. Reducing seed production of small layby weeds in ridge tillage may aid in solving the weed problem in this conservation tillage system.

Seed dormancy does not play a role in the germination ecology of curly dock (Rumex crispus L. ♯ RUMCR). This study confirms reports that freshly matured seeds are nondormant, and it shows that buried seeds exposed to natural seasonal temperature changes remain nondormant. From October 1981 through June 1983, seeds exhumed at monthly intervals germinated 80 to 100% at all thermo-periods. These results do not support suggestions that seeds of curly dock buried in soil enter dormancy. However, the results do explain why seeds of this species in the Beal and Duvel buried-seed experiments germinated when exhumed at various times during the growing season.

The involvement of environmental factors in dormancy cycling is well known in temperate annual species, but it is not known how interaction between soil temperatures and humidity can modulate dormancy in perennial tropical species. In this study the effects were evaluated of substrate temperature and humidity on the modulation of the acquisition and overcoming of secondary dormancy in the buried seeds of two endemic Eriocaulaceae species from the rocky fields (campos rupestres) vegetation in south-eastern Brazil. Fresh seeds of Comanthera bisulcata and Syngonanthus verticillatus were buried and subsequently maintained at temperatures of 15, 20, 25 and 30°C, under three substrate humidity levels (boggy, humid and humid/dry). The seeds were exhumed every 3 months and tested for germination (20°C, 12 h photoperiod) and viability (tetrazolium test). The seeds of both species acquired dormancy after burial in all of the treatments. During the experimental period they demonstrated cycles of acquisition and overcoming of dormancy that were most evident in the treatments involving alterations of the substrate humidity (humid/dry regime) that coincided with the environmental conditions found naturally in the region of origin of the species. The seeds gradually lost dormancy during the dry period and re-acquired it when exposed again to humidity; dormancy would once again be overcome during the subsequent dry period. Burial promoted the acquisition of dormancy in C. bisulcata and S. verticillatus seeds; the lowest temperature tested favoured overcoming dormancy; and varying the humidity regime signalled the acquisition and the overcoming of secondary dormancy.

The dormancy pattern of buried seeds of Datura ferox was studied by testing germination responses to red light (R), far-red light (FR) or darkness after exhumation at regular time intervals. The seeds were deeply dormant at the time of burial in winter. After three months (spring), exhumed seeds began to respond to an R pulse. Summer temperatures did not induce secondary dormancy. During winter of the second year, seed germination after an R pulse increased further; however, germination after an FR pulse or in darkness also increased and reached values close to R. Changes in seed germination after an R or an FR pulse and in darkness were studied in a factorial design experiment, combining different depths of burial (0.5, 5 and 10 cm), presence of vegetation (with or without vegetation canopies), and date of exhumation (4 or 7 months after burial). The seeds placed at 0.5 cm depth did not germinate in any light treatment. A very high sensitivity to light, indicated by the promotion of germination by an FR pulse compared to darkness, was exhibited only in seeds buried at 5 cm in a soil without vegetation. A typical R/FR reversible response was observed in seeds exhumed at 5 and 10 cm in almost all situations of burial; except in a soil without vegetation, at 10 cm depth, in late summer when even dark controls showed high germination. It is concluded that buried seeds of D. ferox are released from dormancy in two steps, the first step during the spring of the first year and the second step during the subsequent winter. This process is not obviously controlled by summer temperatures. The acquisition of a very high sensitivity to light depends on vegetation cover and depth of burial, and thus it is predicted to be affected by agricultural practices.

It has been hypothesized that fluctuations in soil water content may affect the dormancy status of weed seed banks under field conditions. In this paper, we present results showing that fluctuations in soil water content affect the dormancy status of buried seeds of Polygonum aviculare L. stored at dormancy-releasing temperatures. Effects of fluctuations in soil water content on the dormancy status of P. aviculare seeds were evaluated by comparing changes in the range of temperatures and water potentials permissive for germination, and in the sensitivity to fluctuating temperatures, between seeds subjected to a moist soil regime (MS) or to a fluctuating soil water content regime (FS). In comparison to the dormancy release pattern observed for seeds subjected to MS, seeds subjected to FS generally showed an increase in their dormancy level after periods of storage under dry soil conditions, and a decrease in their dormancy level after periods of storage under moist soil conditions. These effects were more pronounced during early stages of the storage period, producing larger changes in the thermal and water potential range for seed germination than in the sensitivity of seeds to fluctuating temperatures. Seeds subjected to FS generally exhibited a lower mean low-limit temperature, lower mean thermal time and hydrotime requirements for germination, and a higher proportion of the seed population with the capacity to germinate in situ, than seeds subjected to MS. The results obtained suggested that fluctuations in soil water content could be an additional factor affecting dormancy and weed emergence patterns under field conditions.