Cistus species have seeds with hard coats which impose physical seed dormancy that can be released after seed scarification. In fire-prone habitats, the break of physical seed dormancy is usually related to the heat produced during fires. It is commonly accepted that most hard-seeded species, including those of the genus Cistus, are able to germinate under a wide range of temperatures in light as well as in darkness, once the seed becomes permeable. However, although many studies have focused on the release of physical dormancy only, a few have done so on the effect of environmental factors once dormancy is released. In this research, through a factorial experiment, we analysed the effects of light (light and darkness) and a range of temperatures (10, 15, 20, 25 and 30°C) on the seed germination of eight Cistus species after a heat shock. On average, almost 60% of the seeds did not germinate despite being viable, and this lack of germination increased with higher temperatures during the treatment. Although an idiosyncratic germination response emerged, temperature had a significant effect in all the species, reaching the highest levels of germination between 10 and 20°C. Light interacted with temperature in four cases by increasing the germination, especially under the least favourable temperatures. Environmental factors, such as temperature and light, appear to modulate the germination of the studied Cistus species after the release of physical seed dormancy.

Experiments investigating mortality in the soil seedbank are aided by using only seeds that are initially viable and capable of remaining ungerminated (hereafter “persistent seeds”). However, seed mortality experiments often use heterogeneous populations containing persistent, nonviable, and germinable individuals. In this investigation we developed and compared nondestructive tests for isolating persistent seeds of two weed species characterized by physical seed dormancy (dormancy imposed by a water-impermeable seed coat): velvetleaf and ivyleaf morningglory. Individual seeds were weighed, steeped in water (hereafter “steepate”) for 48 h, and then assayed for imbibition. These seeds were then subjected to persistence assays conducted under controlled conditions (60 d in hydrated soil under 25/15 C day/night temperatures, 14-h photoperiod). Persistent seeds were less likely to imbibe and more likely to produce steepates with low electrical conductivity compared with germinable and nonviable seeds. For velvetleaf, persistent seeds were best segregated by comparing changes in steepate conductivity during 4 to 48 h of soaking, with the corresponding classification and regression tree (CART) model making few false discoveries (false discovery rate for persistence; FDRp = 8.6%, n = 93) and many true positive classifications (true positive rate for persistence; TPRp = 100%, n = 85). For ivyleaf morningglory, both a change in steepate conductivity from 4 to 48 h of soaking and imbibition status after soaking accurately separated persistent seeds (accuracy measures of corresponding CART models: FDRp = 5.6%, n = 150; TPRp = 100%, n = 142). Thus, for species with physical seed dormancy, we recommend use of steepate conductivity and imbibition status after soaking for isolation of persistent seeds. These seeds can then be used to optimize experiments on mortality in the soil seedbank. Nondestructive tests for isolating persistent seeds of species characterized by physiological seed dormancy require further research.

Dormancy in seeds of Dodonaea viscosa is due to a water-impermeable seed coat (physical dormancy, PY). Thus, mechanically scarified seeds imbibed water (c. 95% increase in mass) and germinated to high percentages over a wide range of temperature regimes in both white light and darkness, whereas non-scarified seeds did not take up water. Dry heat at 80–160°C and dipping in boiling water for 1–60 s also broke dormancy in a high percentage of the seeds, and continuous far-red light was not inhibitory to germination. However, dry storage in the laboratory for >1 year did not overcome dormancy. Seeds made water-permeable by boiling imbibed water, and thus germinated, at a much slower rate than those made water-permeable by mechanical scarification. We suggest that boiling opened the ‘water gap’ in the seed coat (not yet described in Sapindaceae but present in other taxa with PY) and that water entered the seed only through this small opening, thereby accounting for the slow rate of imbibition and subsequent germination. Physical dormancy has now been shown to occur in seeds of this polymorphic, worldwide species from Australia, Brazil, Hawaii, Mexico and New Zealand. The low level of dormancy reported for seed lots of D. viscosa in China, India and Pakistan is probably due to collection of seeds before they dried to the critical moisture content for development of water-impermeability of the seed coat. Germination of non-dormant seeds over a wide range of temperatures and in white light, far-red (leaf-canopy shade) light and darkness are part of the germination strategy of D. viscosa and of other taxa whose seeds have PY at maturity.

The intact germination unit [seed+endocarp, (‘seed’)] of the two species of the Australian endemic genus Stylobasium (Surianaceae, Fabales) is water impermeable. Thus, the seed does not imbibe water or germinate until the integrity of the endocarp, which contains an outer layer of palisade cells, is disrupted. In this study, intact seeds of S. australe and of S. spathulatum, incubated on a moist substrate (for up to 2 years), did not imbibe water, whereas those that were mechanically scarified (both species), or dipped in boiling water for 30 s (S. spathulatum), imbibed and germinated. Thus, seeds of Stylobasium species have physical dormancy (PY). This is the first report of PY in Surianaceae, making it only the sixteenth family of angiosperms (no gymnosperms) in which this class of seed dormancy has been identified.