Totalling more than 3000 species, parasitic angiosperms are a most diverse group of organisms. Classified as either shoot or root parasites according to site of attachment, plant parasites are further classified, according to the degree of parasitism, into one of two divisions: holoparasitic or hemiparasitic. Within these divisions, angiosperm parasites are either obligate or facultative.

Obligate parasites cannot survive to maturity without attaching to a host plant, thus the need to germinate in close proximity to a host first characterizes the specialized germination and seed dispersal strategies of these plants. However, seeds of all species of the rootholoparasitic Orobanchaceae and four genera within the Scrophulariaceae have evolved very specialized germination strategies. Once the seeds have undergone an after-ripening period, they require a prolonged imbibition period at temperatures of approx. 30°C before they acquire the potential to germinate. Minute seeds with very little reserves, they must germinate within millimetres of the host root for successful host attachment and continued survival. To this end, germination only occurs in responseto specific chemical germination triggers released from the host root. In Striga hermonthica (Del.) Benth., the perception of the host-derived trigger results in stimulation of endogenous ethylene production and it is this ethylene that initiates germination. It is proposed that the chemical triggers released from the host be consideredas ‘elicitors’ which function primarily as allelochemicals and that the parasite seeds have become adapted in such a way as to have an absolute requirement for external germination triggers.

The aim of this work was to analyse the capacity for protein synthesis in embryonic axes from long-term-stored maize seeds, including the role of proline. Embryonic axes from seeds stored for 13 years (S) and non-stored seeds (NS) were incubated in nutrient media after application of [14C]proline. Transformation of [14C]proline into other amino acids was analysed by thin-layer chromatography. After 6 h of incubation, no other labelled amino acids were found. Incorporation of 14C into total soluble and cell-wall (proline-rich) proteins was assessed during this period. Incorporation of [14C]proline into specific cell-wall proteins was lower in S than in NS axes.

Studies using [35S]methionine showed that protein synthesis was slower in axes of S than in NS seeds. Analyses of these proteins by gel electrophoresis and fluorography revealed qualitative differences between the [35S]methionine proteins synthesized by both types of axes. The NS: S ratios for the [35S]proteins were larger than those from the [14C]proline assays. These data may be interpreted as an indication of differential deterioration of transcription or translation in the axes during long-term seed storage.

Partial drying of non-dormant seeds had little effect on germination behaviour compared with undried controls. In contrast, partial drying resulted in a marked increase in the germination response of freshly harvested (dormant) seeds of Z. palustris. Partial drying also resulted in a 100-fold reduction in the concentration of gibberellins (GA4+7) required for maximum germination. Although the concentration range of applied abscisic acid (ABA) that permitted germination was unaltered, partial drying increased the final germination percentage at all concentrations tested. The concentration of ABA above which germination was reduced in freshly harvested (dormant) seeds of Z. palustris was 3.16 × 10−7m compared with 10−4m in fresh (non-dormant) seeds of P. coarctata. Changes in the germination response of Z. palustris seeds to applied growth regulators, following partial drying or cold stratification might be explained by similar changes in hormonal status.

The effects of exogenous phaseic acid (PA) on germination and protein accumulation of cultured immature barley embryos were examined. Chemically synthesized PA was racemic, 87% pure and stable over the course of the experiment. Germination was observable in >90% of the untreated embryos after 3 days of incubation, whereas embryos treated with 10μm abscisic acid (ABA) or PA showed no evidence of germination. Buffer extracts from embryos treated with ABA or PA had similar protein profiles when examined by single and two-dimensional electrophoresis. The profiles differed significantly from those of embryos incubated in the absence of the two compounds. Concentrations of α-amylase inhibitor and barley-germ agglutinin (BGA) increased upon treatment of immature embryos with ABA or PA. This was due to de novo synthesis as there was increased incorporation of radioactivity from 35S-labelled amino acids into the proteins in treated embryos. Endogenous ABA content in PA-treated embryos was not significantly different from that in untreated embryos. An analogue of ABA, 2′, 3′-dihydroabscisic acid, which cannot be metabolized to phaseic acid, inhibited germination and caused increased synthesis of α-amylase inhibitor and germ agglutinin. ABA and PA may both be active in promoting responses associated with ABA in barley embryos, but the embryos are more sensitive to ABA.

The sorption isotherm for excised embryonic axes of recalcitrant (i.e. desiccation-sensitive) Quercus robur L. acorns was determined to find the relation between moisture content and water potential. Subsequently, physiological studies on the effect of desiccating the axes to a range of water potentials were undertaken. The respiratory capacity declined steeply after short exposure to water potentials from −5 to −30 MPa. The leachate conductivity increased significantly after exposure to −5 MPa and rose steeply after exposure to between −12 and −40 MPa. Axes were equilibrated at different relative humidities and the proline content showed a 15-fold increase with a peak value at −10 MPa. It was concluded that the critical water potential for initiation of damage was −5 MPa, and that axes accumulated proline as a response to desiccation stress. The embryonic axes from Q. robur behave more like typical vegetative tissue of angiosperms than like orthodox seeds.

Protein composition of sunflower seeds (Helianthus annuus L.) was analysed to identify a possible marker for germination capacity and to evaluate seed viability precociously after harvest and after natural ageing during storage. Electrophoresis on 2-D gels was used to compare total soluble and in vivo synthesized proteins in two seed lots showing different germination capacities. Differences were observed to a greater extent in in vivo protein synthesis profiles than in total soluble proteins. Inhibition of [35S]methionine uptake and incorporation in seeds with low germinability was also observed. The precise relationship between protein composition and prediction of germinability could not be determined. Other aspects such as membrane damage, capacity for protein synthesis and seed lot homogeneity in relation to germination are discussed.

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.

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.

In order to examine the occurrence of a glassy state in the cytoplasm of maize embryos as a function of water content, isolated embryos were examined using spin-probe electron spin resonance. The glass transition temperature was determined at various degrees of hydration (h) in the range 0.05–0.25 g H2O g−1 dry sample weight. The obtained phase diagram indicates that, at standard storage temperature (−5°C), the cytoplasm of embryos drier than 0.15 g H2O g−1 is in a glassy state.

Polyadenylic acid (poly(A)) content of carrot seeds reached a peak at 40 days after anthesis and then declined as desiccation occurred. A further decline occurred in the early stages of germination and was more extensive in seeds harvested whilst still immature. Accelerated ageing of seed led to significant losses of poly(A) and the content declined still further when aged seeds were set to germinate. In seeds harvested whilst immature and then subjected to ageing, the resumption of net accumulation of poly(A), a feature of normal germination, was barely detectable or did not occur.