Endo-β-mannanase (EC 3.2.1.78) is involved in the hydrolysis of mannan-type polysaccharides that are present in plant cell walls, especially those of the seed endosperm. The genes encoding the endo-β-mannanases have been studied extensively in tomato (Solanum lycopersicum), and five genes (LeMAN1, LeMAN2, LeMAN3, LeMAN4 and LeMAN5) and/or their products have been isolated and characterized. LeMAN1, LeMAN2 and LeMAN3 are expressed in tomato seeds, LeMAN4 in the fruit and LeMAN5 in the flower. LeMAN5 and LeMAN2 are now considered to be the same gene, and the former is re-designated as LeMAN2*. Transcripts of LeMANs 1, 2 and 3 are detected only in the endosperm of tomato seeds, and their synthesis is promoted by gibberellic acid. LeMAN4, in the fruit, occurs as LeMAN4a and LeMAN4i genes that encode an active or inactive form of endo-β-mannanase, respectively. LeMAN1–4 enzymes encoded by these genes share 80% similarity in amino acid sequence. In tomato, the leucine amino acid present near to the C-terminus of the endo-β-mannanase is the most important for achieving full activity of the enzyme.

A UK seed conservation collection of Anemone nemorosa L. seeds held at the Millennium Seed Bank (MSB) showed low viability in its first post-storage test. Because achenes of A. nemorosa are naturally dispersed when they are green, we tested the hypothesis that seeds may not be fully desiccation tolerant and storable at the time of natural dispersal, and that a post-harvest treatment could increase the proportion of desiccation-tolerant seeds. Achenes harvested at the point of natural dispersal in late May in 2003 and 2004 were either placed immediately on 1% water agar at 20°C (‘laboratory’ treatment), or placed in nylon sachets and buried in leaf litter among plants growing in the wild (‘field’ treatment). Samples were withdrawn at intervals over a period of 168 d and tested for desiccation tolerance (drying to 0.059 g H2O (g DW)− 1) and longevity (controlled ageing at 60% relative humidity and 45°C). An initial increase, followed by a decline, in the proportion of seeds surviving desiccation and in the longevity of both laboratory- and field-treated samples coincided with the development of embryos from globular to heart- and then torpedo-shaped. Developmental arrest was not required for the acquisition of desiccation tolerance, and continued growth and development of the embryo resulted in a loss of desiccation tolerance, similar to that seen in orthodox seeds upon radicle emergence. Furthermore, while A. nemorosa seeds, like many from the Ranunculaceae family, might be described as having morphological or morphophysiological dormancy, this lack of developmental arrest does not fit with the usual concept of dormancy. The implications of these results for the classification systems of seed-storage behaviour and dormancy, and for the long-term conservation of seeds of A. nemorosa, are discussed.

The germination of developing seeds is very uncommon and is generally associated with deficiencies in abscisic acid (ABA) synthesis or sensitivity. This paper examines the quantitative relationship between the inhibition of precocious germination and endogenous ABA in the embryonic axis (ABAa) of hydrated soybean [Glycine max (L.) Merr.] seeds, isolated after the completion of histodifferentiation and before the beginning of dehydration, as well as the magnitude and evolution of axis sensitivity to endogenous ABA during that period. Developing seeds harvested at 25, 30, 35, 40 and 45 d after anthesis (DAA) were subjected to incubation or washing to induce changes in ABA content. ABA content was measured by radioimmunoassay, using a monoclonal antibody against free ABA. Germinability was measured as the time to 50% germination (t50). Washing and incubation induced eight- and twofold increases, respectively, in the rate of ABAa decline compared with the in planta ABAa decline. The threshold ABAa for inhibition of precocious germination (ABAc) increased slightly from 25 to 40 DAA [1.15–1.66 μg ABA (g DW)− 1]. This contrasted with the substantial decline in ABAa [10.90–2.07 μg ABA (g DW)− 1] during the same period, and indicated that sensitivity to endogenous ABA of hydrated seeds was initially high and diminished slowly during development. The relationship between (ABAa–ABAc) and t50 was linear for immature seeds incubated before and after washing. Below the ABAc, there were no differences in the t50 of 25–45 DAA seeds. The ABAa contribution to the control of precocious soybean seed germination was evident, although other potentially interacting factors were also present.

The stimulatory role of 3-methyl-2H-furo[2,3-c]pyran-2-one, a smoke-derived butenolide, on germination and post-germination events is well documented. Previous studies have involved germinating seeds in the continuous presence of the compound. However, commercial growers cannot exploit the potential of the butenolide for large-scale production of crops due to limited availability and environmental constraints. The present study was undertaken to assess the potential of the butenolide as a priming agent of tomato (Solanum esculentum Mill.) seeds. Flow cytometry data revealed that butenolide-primed seeds had a higher percentage of nuclei at the 4C stage than water-primed seeds. Emergence of the radicle was much faster in the primed seeds. After 36 h of imbibition, a higher percentage of the butenolide-primed seeds (22%) exhibited radicle emergence compared to the water-primed seeds (12%). While butenolide-primed seeds initially germinated more rapidly than either water-primed or unprimed seeds in a 48-h period, water-imbibed seeds reached a similar germination level as the butenolide-primed seeds by 60 h of incubation. The butenolide-primed seeds produced significantly (P ≤ 0.05) more vigorous seedlings than water-primed seeds or seeds in the continuous presence of either water or butenolide. A gradual decrease in the seedling vigour index was recorded for both water and butenolide-primed seeds with increased seed storage at room temperature. Nevertheless, the vigour index was significantly greater in the butenolide-primed seeds than the water-primed seeds. Vigour indices were significantly (P ≤ 0.05) higher for the butenolide-primed seeds under various stress conditions (salinity, osmoticum or temperature) compared to control or water-primed seeds. Results of the present study suggest that the butenolide is a good seed-priming agent. Additionally, primed seeds retained the promotive effect for a considerable time. This was also the case for tomato seeds under various simulated field stress conditions.

Samples of soil and recently deposited sediments were collected from the river bed, bank face and bank tops of two lengths (reaches) of the River Frome, Dorset, UK and one reach of the River Tern, Shropshire, UK. Soil propagule bank samples were collected in May 2003, and depositional samples were collected subsequently over four consecutive 4-month periods between June 2003 and October 2004. The samples were subjected to three emergence trials under drained, waterlogged and submerged conditions. Significantly more seedlings germinated in the drained than waterlogged trial, and waterlogged than submerged trials. Drained, waterlogged and submerged trials identified 186, 76 and 37 species, respectively. Six species identified in the waterlogged trials were not identified in the drained trials, and five species in the submerged trials were not found in the drained trials. Submerged trials added two species to the drained and waterlogged results. Application of detrended correspondence analysis (DCA) to average species abundance data, for the sampled hydrological habitats (bed, bank face, bank top) within the soil propagule bank and four depositional data sets, generated different results for the three trials. The drained treatment revealed significant differences between sites, seasons and hydrological habitats, whereas the waterlogged and submerged treatments presented an increasingly homogeneous view of the samples. Our results confirm other propagule bank emergence comparisons and extend them to depositional samples, demonstrating that the strong environmental sieves imposed by waterlogging and submergence restrict emergence of numerous terrestrial, wetland and even some aquatic species that were successfully identified using the drained conditions.

The size and composition of the seed bank of a rare species (Erica ciliaris L.) was analysed. E. ciliaris hybridizes with a common relative in southern England (Erica tetralix). The seed banks of these co-occurring species were measured at a number of sites with a range of vegetation types and different management histories. Additional sets of samples were taken from forestry plantations on former heathland sites, where these species were known to occur. Relatively few hybrid seedlings were found in any of the seed-bank samples, even though their vegetative abundance within the sampling areas was equal to that of the pure plants. However, the abundance in the vegetation of the two pure species was reflected in the seed-bank size on each of the vegetation types, both with and without burning management. The seed banks from the forestry plantations show that the numbers of seeds of both E. tetralix and the hybrid were depleted, but that the seed bank of E. ciliaris was not significantly different from that of open heathland seed banks. The long-lived nature of the seed bank indicates that there are opportunities for habitat restoration on former heathland sites.

Trials were carried out to investigate natural weed seed burial in a no-till agricultural system. With this aim, 30 important weed species were selected to explore if, and to what extent, seed vertical movement is conditioned by soil texture, cumulative rainfall or by seed characteristics. Without soil tillage, the vertical position of the seeds was only a few millimetres below the surface, but it was dependent on soil texture. Seed burial was much slower (and to lesser depths) in clay soils than in sandy soils. Seeds reached greater depths after 1 year in sandy soil (10% >6 mm) than in clay soils (2% >6 mm). Burial dynamics were also influenced by rainfall and seed weight. The amount of rain necessary to halve weed seeds observable on the soil surface was a function of the soil texture and seed weight; linear regressions between total rainfall amounts and seed weight showed that the slope of the relationship increased as the sand component of the soil decreased (21.1, 35.4 and 39.4 in sandy, loam and silty-clay soil, respectively). A polynomial regression, carried out in sandy soil, between 1000-seed weight and their burial capacity showed an inverse relation (P>0.05) between these two parameters. Seed shape and coat microsculpture also influenced movement, but only minimally.

Four temperature response models were compared describing the emergence rate of Solanum sisymbriifolium (L.) over a broad range of suboptimal temperatures and at different soil water potentials. In the laboratory, the effects were tested on germination rates at constant (9.1–21.8°C) and diurnally fluctuating temperatures at different soil water potentials. Linear, Q10, expolinear and quadratic models were fitted to the data on rate of emergence against temperature. For model validation, field emergence was monitored in 11 sowings conducted in 2001–2004. Emergence rate increased with temperature and was relatively high at soil water potentials in the range of − 0.21 MPa to − 2.6 × 10− 3 MPa, but was almost zero at − 0.96 MPa and − 1.8 × 10− 3 MPa. Diurnal temperature fluctuations did not have a differing influence on germination rates or final germination percentages compared with constant temperatures. The expolinear and the quadratic models were most accurate in explaining variation of laboratory data, especially at temperatures close to the minimum germination temperature of S. sisymbriifolium. These two models had root mean square errors for predicting field emergence rates (5.9 to 38.4 d) of 0.81 and 0.87 d, respectively, and were considered more appropriate to predict the time to 50% germination for crops grown in conditions near their ‘base temperature’ than the widely used linear temperature (thermal time) models. The Gompertz function was fitted to percentage germination versus the time-accumulated germination rate (using the expolinear function to describe the rate–temperature relation). This combined model adequately predicted the temporal pattern of emergence in the field.