Germinating seeds of many species, especially those of tropical or subtropical origin, suffer chilling injury when exposed to low but non-freezing temperatures, resulting in poor seedling establishment and reduction in yield. The severity of injury depends upon several factors such as (i) the species or the cultivars involved, (ii) the initial water content of the seed, (iii) the temperature to which seed is exposed, (iv) the duration of chilling exposure and (v) the period during the course of germination when the chilling exposure takes place. The period of imbibition by seeds is the period of sensitivity to the stresses but especially to chilling temperatures. Imbibitional chilling injury is defined as sensitivity to a combination of low seed-water content and imbibition at cold temperature. The mechanism of chilling injury in seeds is different from chilling injury of hydrated tissues and is discussed in relation to the involvement of membranes, respiration, rate of hydration and the concept of discreet moisture levels. Furthermore, the mechanistic and applied aspects of pre-sowing seed treatments for improved germination performance under chilling stress are discussed with an emphasis on hydration-dehydration, osmotic priming and growth regulator treatments.

Desiccation tolerance is one of the most fundamental properties of seeds. It is acquired late in seed development and is considered necessary for the completion of the plant's life cycle, as an adaptive strategy to enable seed survival during storage or environmental stress, and to ensure better dissemination of the species. The role of water status in desiccated tissues and problems related to testing tolerance in seeds are reviewed. The molecular mechanisms of desiccation tolerance has received extensive consideration only during this past decade. There is a general consensus that desiccation tolerance involves the protection of cellular membranes from the deleterious effect of water removal and the resultant necessity to maintain the bilayer structure in the absence of an aqueous environment. Therefore, some aspects of desiccation-induced membrane injury are described. Several strategies for coping with cellular desiccation have been identified the presence of high amounts of non-reducing sugars, the efficiency of free radical-scavenging systems and the expression of desiccation- and/or ABA-regulated genes. These molecular mechanisms allowing cellular protection are reviewed together with their respective role in dessication tolerance. It is concluded that desiccation tolerance is not likely to be ascribed to a single mechanism but rather to a multifactorial property in which each component is equally critical.

Marrow (Cucurbita pepo L.) seed quality was monitored during seed development and maturation in 2 years. Mass maturity (end of the seed-filling phase) was attained 61–63 d and 54 d after anthesis in 1989 and 1990, respectively, when seed moisture contents had declined to 40–48% (wet basis). Considerable dormancy was encountered during standard germination tests, but was overcome by decoating the seeds. The ability of dried, decoated seeds to germinate normally in standard tests reached near maximal values shortly after mass maturity; these values were more or less maintained in seeds from subsequent harvests. Maximum seed longevity in air-dry storage was detected in seeds harvested 24 d (1989) and 26–31 d (1990) after mass maturity. Seedling dry weights 15 d after sowing were greatest for seeds harvested 2–22 d (basal fruits) or 14 d (apical fruits) after mass maturity in 1989, and were positively correlated (P<0.01) with times from seedling emergence to seedling harvest. Consequently in the subsequent year the hypothesis that these differences in seedling dry weight were solely due to differences in times from sowing to emergence was tested (and confirmed). Seedling relative growth rates did not differ with seed harvest date (P>0.25) in 1990, but absolute seedling size did (P<0.005); seeds harvested 21–31 d after mass maturity had the greatest seedling weight and also growth rate (in absolute terms) at any one time after sowing. Decline in seed quality (when assessed by both potential seed longevity and seedling growth) was not detected until the final harvest interval in 1990 (85–90 d after anthesis, 31–36 d after mass maturity). These results for marrow contradict both aspects of the general hypothesis that seed quality is maximal at the end of the seed-filling phase and that viability and vigour begin to decline thereafter.

Two different pre-emergence treatments preventing radicle protrusion by limiting the extent of imbibition were tested on conifer seeds. Osmotic priming in solutions of polyethylene glycol (PEG) which prevented radicle protrusion during prolonged (3 weeks) treatment resulted in variable percentage germination, mean germination time, and coefficient of uniformity of germination among different seedlots when placed on water. All three germination parameters were either unchanged or inferior in seeds subjected to the various PEG concentrations, treatment temperatures and treatment durations when compared with prechilled controls. In contrast, white spruce and jack pine seeds invigorated at 30% moisture content and 15°C in Gore-Tex membrane tubes consistently germinated faster than prechilled control seeds when subsequently placed on water. Tube invigoration affected neither the ability of seeds to complete germination nor the uniformity of germination. The decrease in mean germination time as treatment duration progressed was always linear and plateaued at approximately 4 days after the tube-invigorated seeds were placed on water regardless of species or seedlot. On average, tube invigoration decreased white spruce mean germination time by 0.13±0.02, and black spruce by 0.23±0.03 day per day of invigoration for up to 20 days of treatment. Jack pine mean germination time decreased 0.2±0.04 day per day of invigoration for up to 14 days of treatment.

It has been proposed that gibberellic acid (GA3) promotes germination by overcoming restrictions in sugar production and utilization in afterripening-responsive dormant caryopses. While their germination rates were similar, germination commenced sooner in afterripened wild oat (Avena fatua L.) caryopses than in dormant caryopses treated with GA3 and dormant excised embryos treated with GA3 plus fructose (Fru). Limited germination occurred in dormant excised embryos cultured with GA3 alone. Carbohydrate concentrations were measured over time in dormant caryopses and excised embryos whose germination was induced with GA3 and GA3 plus Fru. The concentration of sucrose (Suc) in the endosperm declined prior to germination of dormant GA3-treated caryopses. Raffinose (Raf) family oligosaccharides in the embryos of dormant GA-treated caryopses remained relatively constant prior to and shortly after the onset of germination. In contrast, Raf family oligosaccharides in the embryos of afterripened caryopses declined prior to germination. Together this suggests Raf family oligosaccharide utilization is not associated with germination per se. Increased starch levels, which occurred in dormant excised embryos treated with Fru and GA3 plus Fru, were associated with dormancy because similar effects were not apparent in afterripened embryos cultured with Fru. An initial decline in the concentration of Raf family oligosaccharides in dormant embryos cultured with GA3 or GA3 plus Fru seems to be a result of the excision process. GA3 appears to stimulate the germination of dormant embryos by enhancing the uptake or utilization of Fru. It appears that GA3 and afterripening-induced changes in carbohydrate utilization in dormant caryopses are different.

The effect of natural and artificial seed ageing has been compared in terms of physiological and biochemical responses of several maize genotypes. The physiological parameters were: viability, germinability, emergence in sand and dry matter accumulation. The biochemical parameters were: DNA synthesis and DNA polymerase activity. A close and direct relationship was found between seed deterioration and DNA metabolism in all maize materials which responded to ageing according to their genetic constitution; i.e., vigorous genotypes suffered less severe damage or recovery was faster than in the low-vigour genotypes. Coordination of events at appropriate times would seem a critical factor for proper seed germination.

Wheat (Triticum aestivum L) seeds contain a proteinaceous α-amylase inhibitor. We estimated the amount of the inhibitor that can bind to α-amylase rather than the total amount of the inhibitor, using an ELISA method. During 48 h of imbibition, the amount of the inhibitor did not change, while α-amylase activity increased rapidly. These results suggest that α-amylase synthesized de novo does not bind to the inhibitor. To examine further the interaction between α-amylase and its inhibitor, we localized immunohistochemically both α-amylase and the inhibitor in germinating seeds. In the embryo, we observed α-amylase only in the scutellar epithelial cells at 24 h after the start of imbibition, and later in the scutellar parenchyma cells. The inhibitor, on the other hand, was present between the scutellar parenchyma cells of the embryo at 0 h and 24 h after the start of imbibition, and disappeared later. α-amylase is separated from the inhibitor in the embryo. In the endosperm, we detected α-amylase in the aleurone cells at 24 h after the start of imbibition and later in the starchy endosperm. The inhibitor was present in the aleurone cells and starchy endosperm of the dry seed. During imbibition, the inhibitor in the starchy endosperm disappeared from the area to which α-amylase was secreted. It appears that α-amylase in the starchy endosperm also does not interact with the inhibitor. The aleurone cells are the only place that α-amylase can come into contact with the inhibitor. But, early secretion of α-amylase from the aleurone cells after imbibition started, and rapid disappearance of the inhibitor in the aleurone cells suggest that the α-amylase inhibitor does not work as an effective inhibitor of the endogenous α-amylase synthesized following germination.