Books and review articles in various areas of ecology and seed and plant biology continue to report that dormancy-break in seeds (and fruits) with water-impermeable coats (i.e. physical dormancy) occurs via soil-microbial action and/or abrasion by soil particles. However, there is little evidence in the scientific literature to support these assumptions, which, in fact, do not make good evolutionary sense for two related reasons. First, several types of anatomically specialized water-restriction structures have evolved as part of the seed or fruit coat of taxa with physical dormancy. These structures act as ‘signal detectors’ of physical-environmental changes that cause seeds (and fruits) to become water-permeable only at these sites, in seasons and habitats in which there is a good chance that some seedlings will become established. Second, seed (and fruit) coat breakdown by microbial action or by abrasion likely would occur in seasons and habitats in which seedlings could not survive, thus lowering the fitness (λ) of the plant taxa in question.

A commercial liquid smoke (LS) flavoring product (Reese Hickory brand) in aqueous dilutions of 4–5% (v/v) broke dormancy (40–100% germination) of both intact and dehulled red rice (Oryza sativa). To elicit this response in intact grains, the glumes had to be pricked with a dissecting needle following contact with LS and water rinsing. Germination percentages rose with increasing contact time (up to 7 d), and grains first imbibed with water before transfer to LS showed similar germination percentages as those first incubated with LS before transfer to water. LS dilutions were highly acidic (about pH 3). Dormancy-breaking activity of LS was pH-dependent and was reduced at pH values of 5–7. Buffer controls remained dormant irrespective of pH value. Maximum activity varied primarily among different bottles of LS and only to a minor extent between red rice seed lots. Dry-afterripening at 30°C for up to 14 d increased the sensitivity of unpricked, intact grains to LS compared with water controls. LS concentrations that broke dormancy of intact grains partially inhibited germination of nondormant, fully afterripened grains. Storing grains in containers of flooded soil increased sensitivity to both LS and pricking. Nitrite levels in LS were negligible and insufficient to account for the bioactivity of LS.

Seed storage proteins were analysed in 27 varieties of alfalfa (Medicago sativaL.); these included five subspecies (glomerata, caerulea, falcata, hemicycla, praefalcata), seven of the nine sources of Medicago germplasm introduced into North America and a sample of additional cultivars. The protein patterns were remarkably consistent for all of these taxa. One-dimensional and two-dimensional gel electrophoresis revealed only minor differences in polypeptide composition within each of the three major classes of storage protein (7S globulin, 11S globulin, 2S albumin). The slight variations that were found provided no information on either parentage or evolutionary relationships amongst these particular taxa. Nonetheless, persistent and reproducible heterogeneity of some minor polypeptides of 11S globulin (medicagin) may be useful under other circumstances for cultivar identification in alfalfa. Both subfamilies (I and II) of the 11S globulin were strongly expressed in all of the cultivars and subspecies examined. It was concluded that this structural divergence within the 11S storage protein family predated the evolution of the M. sativa L. species complex. Most of the variability in storage proteins was quantitative. However, even this variability was reduced when data were standardized with respect to seed dry weights. The consistent similarities in qualitative and quantitative expression of seed storage proteins amongst all of these taxa suggest a high degree of uniformity in both seed physiology and genetics within the alfalfa species complex.

The performance of cucumber (Cucumis sativus L.) seeds in relation to ovary and ovule position was monitored during seed production. Seeds from three (first, seventh and tenth nodes) fruit positions and three (stylar, intermediate and peduncular) ovule positions were harvested serially during development and characterized with physiological and cellular markers. Seed moisture contents declined to 30%approx. 35 d after pollination (DAP) and remained constant thereafter. At 42 DAP the maximum dry weight was acquired in seeds except those from peduncular segments, whose dry weight accumulation lagged behind. The onset of germinability and desiccation tolerance occurred before the attainment of maximum dry weight, whereas seed performance, as shown by laboratory germination and greenhouse emergence, was largely improved after the completion of seed development. Cell cycle activities (DNA per nucleus and β-tubulin content) ceased by 28 DAP, whereas the degradation of seed chlorophyll continued during the entire maturation period. Seeds from the top fruit and from the peduncular fruit segments were delayed in reaching maximum quality compared with seeds from other positions, and this was correlated with a slower decline of chlorophyll fluorescence.

Seeds of Cenchrus ciliaris L. were produced under different hydro–photo–thermal environments with and without fertilizer. Dormancy loss of spikelets and extracted caryopses was tested during dry after-ripening at 40°C and 43% equilibrium relative humidity. Caryopses had higher initial germination and lost their dormancy faster than spikelets. Dormancy of both caryopses and spikelets generally decreased with an increase of maturation temperature and fertility, whereas dormancy increased if water stress was imposed during maturation. The latter effect was smaller when the mother plants were exposed to water stress after caryopses were fully formed than when water stress cycles were applied throughout maturation. Daylength extension (to 14 or 18 h d-1) by artificial light increased dormancy of both caryopses and spikelets. The effect of long days declined when plants were exposed to natural daylight for more than 10 h d-1. The after-ripening curves were consistent with the hypothesis that dormancy periods of individual seeds are normally distributed within each seed lot. Rates of loss of dormancy were quantified by the slopes of these curves. In a given experiment, these rates were identical for caryopses but not always for spikelets that matured in diverse environments. Even for caryopses, however, the slopes varied between experiments. Therefore, the results do not support the hypothesis that a dormancy model can be applied universally to all seed lots of Cenchrus ciliaris. Methods of predicting the period of after-ripening required to achieve desired levels of dormancy for reseeding degraded rangelands are discussed.

Dormancy-breaking requirements and types of dormancy were determined for seeds of Lonicera fragrantissima Lindl. & Paxt., L. japonica Thunb., L. maackii (Rupr.) Maxim. and L. morrowii A. Gray. Seeds of all four species have underdeveloped spatulate embryos that are about 20–40%fully developed (elongated) when dispersed. Embryos in freshly matured, intact seeds grew better at 25/15°C than at 5°C. Gibberellic acid (GA3) (tested only in the light) was more effective in breaking dormancy in L. maackii and L. morrowii than in L. fragrantissima and L. japonica. Warm- followed by cold stratification was required to break dormancy in seeds of L. fragrantissima, whereas seeds of L. japonica required cold stratification only. Thus, seeds of L. fragrantissima have deep simple morphophysiological dormancy (MPD) and those of L. japonica nondeep simple MPD. About 50%of the seeds of L. maackii required warm- or cold stratification only to come out of dormancy and 50% of those of L. morrowii required warm stratification only, whereas the other 50% did not require stratification to germinate. Thus, about half of the seeds of the two species has nondeep simple MPD, and the other half has morphological dormancy (MD). In these laboratory tests, seeds of L. japonica, L. maackii, and L. morrowii generally germinated to significantly higher percentages in light than in darkness; seeds of L. fragrantissima were not tested in darkness. Peaks of germination for seeds of L. fragrantissima, L. japonica, L. maackii and L. morrowii sown on a soil surface and covered with Quercus leaves under near-natural temperature conditions shortly after seed maturity and dispersal in late June 1997, late November 1997, early November 1996 and late June 1998, respectively, occurred in early March 1998, late February 1998, late March 1997 and early October 1998, respectively. The germination phenologies of seeds of the same species and seed lots buried in soil were similar to those of seeds under leaf litter. High percentages of seeds of all four species germinated both under litter (78–96%) and beneath the soil surface (78–97%). These germination patterns correspond closely with the requirements for embryo growth and dormancy break in the four Lonicera species.

In Britain, Lobelia urens (L.) (the heath lobelia) occurs in rough grassland, is rare and only found in southern England, where it is at the northern limit of its range. Emergence and survival of L. urens was investigated at six locations in two geographically distinct sites experiencing spring, autumn or no grazing in two consecutive years. Four factors were evaluated qualitatively, as a means of characterizing microhabitats for germination and survival: all permutations of higher plant cover, bryophytes, plant litter and surface depressions. The potential effect of adjacent plants on recruitment was also assessed using the nearest neighbour distance (NND). Grazing created depressions, removed plant litter and increased the proportion of sites with higher plant cover. It also resulted in a more open sward with higher NNDs. None of these changes stimulated recruitment. Instead, small increases in the frequency of some rare or very rare microhabitat types were vital in making grazed rough grassland more suitable for emergence. Reduced litter loads and a greater quantity of moss were two key responses. Overall, survival of L. urens was less than 1% and was particularly favoured by moss and an increase in NNDs. Shading from higher plants, with or without plant litter, decreased emergence, but the precise role of litter was complex and most probably related to its quantity. In an experimental seed bed, only empty depressions favoured emergence. The microhabitat relationships of L. urens were unusually consistent among locations and consecutive years. L. urens requires high soil surface temperatures but also adequate water for large scale recruitment, and such conditions are encouraged by grazing. The particular problems of experimental design and statistical analysis of data from recruitment experiments are also discussed.

Germination of native tree and shrub species from seed can be unpredictable. Germination of Rosa corymbifera ‘Laxa’ was 2% under normal commercial conditions. This was obtained in the presence of the natural microflora found on the seeds. The microflora originated on the hips and the seeds become inoculated during extraction. Exclusion of microbes from such pretreatments resulted in no germination. Inoculation of surface sterilized seeds with members of the natural microflora resulted in 3% germination. The addition of GarottaTM, a commercial compost activator, to the commercial pretreatment increased germination to 95%. This high germination percentage was sustained over a 5 year period using seeds from the same stock bushes. Addition of the compost activator resulted in a 20-fold increase of microbial activity in the pretreatment mixture, indicating that enhanced microbial growth resulted in higher and more predictable germination percentages.

Germination responses of nonstratified (conditionally dormant) and of cold-stratified (nondormant) seeds of three Solidago species were tested in darkness at 30/15°C following various lengths of exposure [0 (control), 5 and 30 min, 1, 6 and 14 h] to green (mostly 500–600 nm) or white (400–700 nm) light. Prior to exposures, nonstratified seeds were imbibed in darkness at laboratory conditions for 24 h, and cold-stratified seeds were kept in darkness at 5°C on a moist substrate for 8 wk. Nonstratified seeds of S. altissima, S. nemoralisand S. shortii germinated to 0–46%, 0–25% and 36–99%, respectively, in darkness following 5 min to 14 h of green or white light, whereas cold-stratified seeds germinated to 53–98%, 31–85% and 82–100%, respectively. Thus, sensitivity of seeds to both green and white light increased as they passed from conditional dormancy to nondormancy. Moreover, sensitivity to green and white light was similar to the hierarchy of seed size. Green safe lights must be used with caution in interpreting the results of studies on light/dark responses of seeds.