A high-molecular-weight aspartyl proteinase complex, sensitive to pepstatin A was purified to near electrophoretic homogeneity from dry seeds ofjack pine (Pinus banksiana, Lamb.). Two partial activities, endo-and exo-proteinolytic, were associated with the complex, judged by the analysis of haemoglobin hydrolysis products. The high activity of this enzyme in dry jack pine seed suggests a possible function in early germination.

Mature seeds of Norway maple (Acer platanoides L.) are tolerant of desiccation, at least to moisture contents of about 7% (fresh weight basis), but those of sycamore (Acer pseudoplatanus) are killed by drying below about 45% moisture content. Sycamore seeds are thus recalcitrant; while the classification of those of Norway maple as orthodox is confirmed by the fact that between 19% and 7.5% moisture content their longevity is increased in a predictable way by reduction of seed moisturecontent. However, the period of useful storage of the latter in seed banks may be much less than for many crop species. The rates of water loss to a dry environment of both fruits and seeds of sycamore are much less than those of Norway maple, suggesting a degree of desiccationavoidance in the desiccation-intolerant species. Seed physiological maturity (maximum dry weight) occurred 2–3 weeks earlier in Norway maple than insycamore, but in both species this occurred about 150–160 days after peak flowering. Tetrazolium staining is a good indicator of embryo viability in both species, correlating well with germination test results. In Norway maple both methods of viability testing indicated that whole-seed desiccation tolerance coincided with the attainment of maximum dry weight. Tetrazolium staining indicated the development of desiccation tolerance in the radicles/hypocotyls of both species approximately 2–4 weeks before physiological maturity. Possible correlation between changes in the level of embryo dormancy during development and the acquisition of desiccation tolerance are discussed.

Seed development and changes in germination ability and longevity were monitored in control and shaded spring barley (Hordeum vulgare L.)crops grown in two contrasting years. Shading reduced seed dry matter accumulation rates by 24–28% and delayed maturation drying slightly, but had little effect (0–2 d) on the timing of physiological maturity (end of the seed-filling period); final seed dry weights were 76–85% of controls. Moisture contents (wb) at physiological maturity were 48–55%; final mean seed dry weights in the controls were 40.9 mg(S.E. 0.6) in 1988 and 35.2 mg (S.E. 0.5) in 1989. Shading had little orno effect on germination ability or longevity in either year. Seeds fromthe first harvest were viable when dried below 15% moisture content despite being only 34% (1988) to 63% (1989) filled; desiccation promoted germination. Maximum germination achieved after forced desiccation occurredin seeds harvested 7–10 d (1989) to 11–13 d (1988) after physiological maturity, with little subsequent change during the following 14 (1988) or 27 d (1989). Longevity continued to increase during development until a maximum was reached 18–20 d (1988) to 27 d (1989) after physiological maturity (at moisture contents on the mother plant of 18–19% and 14–15%, respectively). In both years, the longevity of these seeds was greater (P<0.005) than that of seeds harvested either subsequently or earlier at physiological maturity. The results contradict the hypothesis that maximum seed quality coincides with physiological maturity and thereafter declines. Rather, maximum seed quality was attained close to when barley seed crops can be combine harvested The subsequent decline in potential longevity on the maternal plant in the field was quantitatively similar to that expected during post-harvest storage.

The field emergence ability of a total of 88 seed lots of spring barley (Hordeum vulgare L.) harvested serially during development in 2 years was compared, as was the size of the resultant seedlings. For seedsproduced in each year, field emergence and the mean dry weight of emerged seedlings were significantly greater for seed lots harvested some timeafter physiological maturity (end of the seed-filling period) than for those harvested at or before this developmental stage. This is compatiblewith results for the potential longevity of these lots. It is concluded that barley seed quality continues to increase after physiological maturity, and that the developing seeds attain maximum quality (however this is assessed) close to when the seed crop can be combine harvested. Positive correlations were detected between seedling emergence and seed dry weight (P<0.05) and between the mean dry weight of emerged seedlings and seed dry weight (P<0.005) among seed lots harvested close to when maximum quality was attained in four seed production environments.

Dormancy in rice (Oryza sativa L.) seed is imposed by certain physical and chemical factors associated with its covering structures, i.e.hull and pericarp. The nature of these germination blocks, their mode ofaction, and processes regulating the release of dormancy are not fully understood. Of nine rice cultivars studied, Ching-shi 15, Stejaree 45, PTB10, and Mahsuri are weakly dormant, and Bansphul, Benaful, Kataktara, Dular, and N22 are dormant. Release of seed dormancy in rice by various treatments, oxidative processes and enzymic changes associated with dormancy, and parallelism between natural and artificially imposed dormancy patterns were examined. The influence of the hull in imposing dormancy was stronger and more prolonged than that of the pericarp. Application of GA3 was effective in inducing germination only in weakly dormant cultivars. Dormancy was completely released in all cultivars by subjecting the seeds to moist heat treatment, by removing the hull and pericarp, and by applying GA3 after dehulling. Dormant cultivars had higher O2 uptake rate and peroxidase activity and lower amylase and dehydrogenase activities than the weakly dormant ones. Hull removal substantially decreased peroxidase activity but enhanced amylase and dehydrogenase activities. Nonanoic acid (C90), a short-chain saturated fatty acid (SCSFA), when exogenously applied to non-dormant seeds imposed dormancy. Dry heat treatment or presoaking in 0.01 m KNO3 or 0.1 m H2O2 was very effective in releasing SCSFA-imposed dormancy. Amylase activity was greatly reduced by treatments with nonanoic acid (C90) or ABA. Considering earlier reports and results of the present study, it is proposed that seed dormancy in rice is regulated both by the presence of SCSFAs and ABA in the hull and the pericarp. The relative significance of these substances in cultivars of tropical and temperate origins and its implications in terms of ecogeographic adaptability are discussed.

The capacity for protein synthesis in embryonic axes of Phaseolus vulgaris L. cv. Top Crop seeds was reduced markedly by soaking in airsaturated and CO2-saturated water. The former treatment induces soaking injury while the latter treatment prevents injury. After soaking, the capacity for protein synthesis in axes of seeds soaked in air-saturated water declined and the pattern of synthesis remained almost similar to that at the time of termination of soaking. However, the capacity and pattern of protein synthesis in axes of seeds soaked in CO2-saturated water recovered subsequent to soaking and approached that of non-soaked seeds.