Germination of field dodder (Cuscuta campestris Yunck.) was investigated in field and laboratory studies. Germination plots established to simulate field conditions showed a rapid decline in the number of seedlings emerging over a 5-yr period. Less than 10% of the seeds planted emerged. Time of germination was correlated with temperature. The dormancy of seeds buried at various depths was found to be broken by overwintering. Older seeds and those close to the surface germinated best. Scarified seeds did not germinate at 15 C nor at temperatures of 39 C or above. Maximum germination occurred at 30 and 33 C. Scarified seeds planted at various depths failed to emerge from 3.8, 4.0, or 7.6 cm in the three soil types evaluated; the majority emerged from 3 cm or less. Seeds stored outdoors, at 3 to 8 C, or −3 to 0 C declined in dormancy with time compared to seeds stored at 15 to 25 C.

Seeds of eight weed species were heated for up to 7 days at 40, 50, 60, and 70 C in dry (2% moisture) and moist (19% moisture) Bosket very fine sandy loam to determine temperature-time treatments lethal to weed seeds. Seeds in dry soil were very tolerant to 60 C or less for up to 7 days but most seeds were killed at 70 C after 7 days. In moist soil, a few (1 to 12%) seeds of common purslane, redroot pigweed, johnsongrass, and spurred anoda survived for up to 3 days at 70 C. Some (4 to 30%) seeds of velvetleaf, pitted morningglory, and the above species survived up to 7 days at 60 C. No seeds of prickly sida and common cocklebur survived more than one-half day at 60 C. Three days at 50 C were lethal to all cocklebur seeds. Many of the sublethal treatments promoted germination of prickly sida, velvetleaf, spurred anoda, and pitted morningglory, presumably because high temperature broke dormancy of some hard seeds. The enhanced effect of heat treatments upon seeds in moist soil compared to seeds in dry soil was due to the higher moisture content of seeds, or in fruit tissues of dispersal units in moist soil. Because some seeds survived several days in moist soil at 60 and 70 C, it is unlikely that soil solarization or other natural methods of raising soil temperature will eliminate weed seeds from the field. However, high soil temperatures may reduce weed seed populations by killing heat-susceptible seeds and by breaking dormancy of hard seeds followed by thermal kill of seedlings.

Germination and longevity of weedy and three domestic okra [Abelmoschus esculentus (L.) Moench. # ABMES] cultivars were investigated. Hard seed coats are the major reason for okra seed dormancy. Hard seeds of weedy okra, induced to germinate by scarification of seed coats, produced plants yielding 94 to 99% hard seeds. Of these, 40% remained hard but viable after overwintering in the soil at 5 cm deep. Nonhard seeds of weedy okra produced plants that yielded 95 to 99% hard seeds, but only 20% remained hard after overwintering in the soil at 5 cm deep. The ‘White Velvet’ cultivar of okra produced a few hard seeds, but none survived longer than 3 months in the soil. The other domestic cultivars, ‘Dwarf Green Long Pod’ and ‘Clemson Spineless', produced no hard seeds. None of these seeds survived over winter in the soil. Some seeds of White Velvet became slightly harder during dry storage based on time in concentrated H2SO4 necessary to induce 80% germination. Although the hard-seed trait existed in the population of this domestic cultivar, it is unlikely that the seeds would overwinter. Seeds that overwinter in a dry condition may be the exception. Because a high percentage of hard seeds overwinter and germinate the following spring, weedy okra has the potential to become a persistent problem.

The seeds of three medics (Medicago orbicularis, M. rigidula and M. rotata) and three clovers (Trifolium stellatum, T. campestre and T. tomentosum) were collected from a pasture in north-west Syria on three occasions: immediately after seed set, at the end of the dry season, i.e. 4 months after seed set, and 16 months after seed set. Complete and sectioned seeds were observed with a scanning electron microscope. Morphological changes and differences in thickness of the seed coat were related to the hard-seededness of the samples collected in the seed bank before the onset of the rainy season. The morphology and structure of the seed coat of all six species were typical of papilionoid legumes. The species with the softest seeds (T. stellatum) showed a very thin and discontinuous cuticular layer at seed maturation (0.16 μm), while a thick and continuous cuticle (4.24 μm) was characteristic of the hardest-seeded species (M. orbicularis). The lens region of seed of all species except T. campestre was weakened after a few months in the field. This weakening was also found in seeds which were certainly hard, but the cracks in the lens region were apparently not deep enough to allow imbibition. Even when large areas of the palisade layer were removed from the lens region of seeds of M. rotata, this was not sufficient to permit water uptake. Differences in the seed coat thickness of the six species accounted for differences in seed dormancy only when seed mass was taken into account.

Six pasture legumes, common in Syrian grasslands, were investigated. Medicago orbicularis and M. rotata had the largest number of hard seeds, with >90% still hard 5 months after shedding; Trifolium stellatum had the least with <30% of hard seeds; T. campestre, M. rigidula and T. tomentosum were intermediate. Hard-seededness in M. orbicularis and M. rotata varied between years. Scarification of hard seeds resulted in almost complete germination in all species. Alternating temperatures (10/20°C) reduced the rate of germination of scarified T. campestre seeds, but had no effect on germination of scarified or unscarified seeds of T. stellatum. The breakdown of hard-seededness in the field in Syria did not begin until 3 months after shedding and greatly increased when seeds overwintered. Breakdown of hard-seededness was slower when seeds were buried at 5 and 10 cm than when seeds remained on the soil surface. Seedling emergence after the rains started in November was highly correlated with the number of soft seeds observed in October. Similarly, a high correlation was found between the percentage of hard seeds in October and carry-over in the seed bank. In small-seeded species (Trifolium spp.), 39% of the initial seed bank was lost in 2 years by causes other than emergence as seedlings. Such losses were only 7% in larger-seeded species (Medicago spp.). The implications of hard-seededness on the utilization and survival of legumes in grasslands are discussed.

Previous studies on several floras have shown that species with small, rounded seeds tend to accumulate persistent seed banks in the soil, while species with larger, less compact seeds do not. The suggested underlying mechanism is predation. Small seeds experience less predation and are more likely to become buried, which itself offers significant protection from predation by vertebrates. The relationship between seed size and shape and persistence in the soil was examined for the flora of the Arasbaran Protected Area in northwest Iran. Seed size was related to persistence in the soil in Iran in the same way as in most other floras examined, but seed shape was not. It is suggested that predation prevents persistence of large seeds in most floras. Where large-seeded persistent species predominate, for example in Australia and (to a lesser extent) in New Zealand, other factors may interfere with the relationship between seed size and predation.