Sycamore Seeds Research Articles

Changes in abscisic acid levels in embryo axes of Norway maple and sycamore seeds during maturation and dehydration

Changes in the abscisic acid (ABA) levels in embryo axes of seeds, belonging to the orthodox (Norway maple — Acer platanoides L.) and recalcitrant (sycamore — Acer pseudoplatanus L.) categories, were investigated throughout maturation using an ELISA (enzyme-linked immunosorbent assay) test. Concentration of ABA in embryo axes substantially differed depending on species and sampling date. ABA was always higher in Norway maple except at the end of seed maturation when ABA content was similar in both species. During maturation ABA decreased in both species but the decline was more marked in Norway maple than in sycamore (11 vs. 3 fold). These species also differed in the pattern of ABA changes, which in sycamore embryo axes was very regular, while in Norway maple a sharp decrease was recorded after acquisition by the seeds of tolerance to desiccation. Dehydration of embryo axes of Norway maple caused a further significant decrease of ABA level. In contrast, in dehydrated sycamore embryo axes ABA content did not decrease, but slightly increased. The role of ABA in desiccation tolerance and dormancy of Norway maple and sycamore seeds is discussed.

Carbohydrate metabolism in Norway maple and sycamore seeds in relation to desiccation tolerance

Summary The work reports on sucrose and oligosaccharide metabolism in Norway maple (Acer platanoides L.) and sycamore (Acer pseudoplatanus L.) embryo axes and cotyledons during seed maturation. Enzyme activities of sucrose synthase (SuS), sucrose phosphate synthase (SPS), acid and alkaline invertases, α-galactosidase and galactinol synthase (GS) were studied. These species are closely related, but differ with regard to seed tolerance to desiccation. Norway maple possesses strictly orthodox seeds, while sycamore seeds are recalcitrant. In contrast to sycamore, maturation of Norway maple seeds was associated with an increase in raffinose and stachyose concentrations and a decrease in sucrose to oligosaccharides ratios. Activities of SuS and SPS as well as α-galactosidase were higher in seeds of sycamore compared to Norway maple. The activity of GS in Norway maple seeds was higher than in sycamore and was coincident with increased level of raffinose and stachyose in mature seeds. The results confirmed a finding of increased sucrose metabolism during maturation in recalcitrant sycamore seeds compared to orthodox Norway maple seeds.

Putative desiccation tolerance mechanisms in orthodox and recalcitrant seeds of the genusAcer

AbstractRecalcitrant seeds are shed moist from the plant and do not survive desiccation to the low moisture contents required for prolonged storage. It has been widely hypothesised that during desiccation of these seeds a stress induced metabolic imbalance develops that leads to free radical mediated damage and viability loss. We investigated this hypothesis in a comparison of two sympatric species ofAcerduring late seed development and post-harvest desiccation:A. platanoides(Norway maple) has orthodox seeds andA. pseudoplatanus(sycamore) has recalcitrant seeds. In both species, respiration rates declined to similar levels at shedding, and the extent of defences against free radicals appears no less in sycamore than that in Norway maple. During drying there was no evidence for the accumulation of a stable free radical, increased lipid peroxidation or decline in free radical scavenging enzymes in either species. In addition, there was a very similar, large increase in total tocopherol in both species. This increase in sycamore was largely of alpha-tocopherol, whereas in Norway maple the increase was largely from its precursor, gamma-tocopherol. Arguably this suggests a similar mechanism in both species, but increased oxidative stress in sycamore. In general, the results suggest that, although damage resulting in viability loss was clearly taking place, the limitation to desiccation tolerance did not result from inadequate free radical scavenging. Soluble carbohydrates and dehydrin-like proteins were also measured during late seed development and drying in sycamore and Norway maple. The greater concentrations of sucrose, raffinose and stachyose and amounts of dehydrins in the radicles and cotyledons of Norway maple compared with those in sycamore was consistent with greater desiccation tolerance in the former. Sycamore seeds are dormant and at the tolerant end of the continuum of desiccation sensitivity among recalcitrant species, and this may account for their different response to that of the seeds of other more sensitive recalcitrant species studied.

Changes in soluble sugars in relation to desiccation tolerance and effects of dehydration on freezing characteristics of Acer platanoides and Acer pseudoplatanus seeds

The role of soluble sugars in desiccation tolerance was investigated in seeds of two species from the genus Acer: Norway maple (Acer platanoides L.) — tolerant and sycamore (Acer pseudoplatanus L.) — intolerant to dehydration. During two years of observations it was found that seeds of Norway maple acquire desiccation tolerance at the end of August i.e. about 125 days after flowering (DAF). During seed development, the transition from intolerant to tolerant state in Norway maple seeds was accompanied by the accumulation in seed tissues of raffinose, stachyose and sucrose. The sucrose/raffinose ratio in Norway maple seeds was lower than in sycamore. In mature Norway maple seeds sucrose and raffinose contents were higher than in sycamore. It was concluded, that soluble sugars such as sucrose, raffinose and stachyose may play an important role in desiccation tolerance and/or intolerance of Norway maple and sycamore seeds. Differential thermal analysis (DTA) was used to study the relationship between desiccation sensitivity and the state of water in seed tissues. The level of non-freezable water was the same in both analysed seed species, but the temperature of water crystallization during desiccation was lower in sycamore seeds.

The effects of desiccation on seed survival in Acer platanoides L. and Acer pseudoplatanus L.

AbstractMature 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.

A comparison of maturation drying, germination, and desiccation tolerance between developing seeds of Acer pseudoplatanus L. and Acer platanoides L

SUMMARYDifferences in maturation drying and desiccation tolerance during seed development were detected between the two contrasting Acer spp., Norway maple (Acer platanoides L.), which shows orthodox seed storage behaviour, and sycamore (A. pseudoplatanus L.), which shows recalcitrant seed storage behaviour. In both species, the onset of germinability (150 d tests at 5 °C) occurred after percentage seed moisture content had begun to decline, but before net loss in seed moisture. The onset of germinability in Norway maple occurred 4 wk before physiological maturity (i.e. 4 wk before the end of the increase in seed dry matter), whereas in sycamore it occurred some ten weeks before physiological maturity when the seeds were only 60 % filled. Seeds of Norway maple were able to tolerate enforced rapid desiccation to 10% moisture content (f. wt) at physiological maturity, when maturation‐drying had reduced seed moisture content to 54 %. Between 2 and 4 wk later seed moisture content rapidly declined naturally to 25 %, at which value the fruits were shed. In contrast, a constant rate of maturation‐drying was observed in sycamore. The seeds were shed at 58 % moisture content and, in almost all cases, the seeds were intolerant of rapid desiccation to c. 10 % moisture content throughout seed development. A very small proportion of sycamore seeds did survive rapid desiccation when harvested between 6 September and 4 October, but no seeds survived desiccation to 5 % moisture content or below. A comparison of the germination of sycamore seeds harvested on four dates and dried to various moisture contents showed that the seeds tolerated greater desiccation as they matured between 12 July and 20 September, but there was no further change thereafter. The results are therefore compatible with previous classifications of seed storage behaviour in each species, and with the view that the initial decline in seed moisture content stimulates the developmental switch which results in the onset of germinability in both orthodox and recalcitrant seeds.

Collection and Care of Sycamore Seeds

Abstract Seeds of low quality will yield seedlings of low quality (and high production expense) in the nursery. No treatments exist that can turn poor seeds into good ones. To help insure a supply of good sycamore seed, remember these key points: (1) delay collections until fruits are mature; (2) dry fruits properly for extraction; (3) clean the extracted seeds well, and because of the fine hairs, take safety precautions to avoid inhalation; (4) upgrade the seed lot; (5) store seeds at 0° to 5° C. and 5- to 10-percent moisture content; and (6) have seeds tested properly.

Seed Dormancy inAcer

Changes in germination inhibitors, cytokinins, and gibberellin-like substances during the breaking of coat-imposed dormancy of sycamore seeds at low temperature suggest that dormancy may be controlled by the presence of endogenous germination inhibitors. Stratification at 5°C led to a greater loss of neutral inhibitor(s) from the embryo than did incubation at 20°C. No marked differences were observed in the level of cytokinins and gibberellin-like substances between treatments. However, a gradual decrease in the level of cytokinins was observed during stratification. Whether a cytokinin-inhibitor interaction is involved in the control of dormancy of sycamore seeds, as was previously suggested, remains to be determined.

Maturation of Sweetgum and American Sycamore Seeds

Maturation of Sweetgum and American Sycamore Seeds

Seed dormancy in Acer: Endogenous germination inhibitors and dormancy in Acer pseudoplatanus L.

Dormant seeds of Acer pseudoplatanus L. contain two zones of inhibition on paper chromatograms in "10:1:1" as detected by the lettuce and cress seed germination, and the wheat coleoptile bioassays. One zone at Rf 0.6-0.8 was partitioned into ethyl acetate at acid pH and was shown to contain ABA by its behaviour on GLC and isomerization under ultra-violet light. The other zone at Rf 0.9 was detected only in the germination bioassays and was partitioned into ethyl acetate over a range of pH indicating the presence of one or more neutral compounds.The inhibitors present in the embryo of dormant sycamore seeds inhibited the germination of non-dormant sycamore seeds at relatively low concentrations. A comparison with the effects of application of exogenous ABA indicated that endogenous ABA could not solely account for the inhibitory activity of seed extracts, which appeared to be due partly to the presence of ABA and partly to that of neutral compounds present in the embryo. Leaching treatments that removed dormancy led to a decrease in the level of inhibitors present mainly in the basic fraction. The exogenous application of kinetin to dormant sycamore seeds increased germination whereas gibberellic acid had no effect. Similar responses were obtained with lettuce seeds inhibited by the basic fraction of dormant sycamore seeds.It is suggested that an inhibitor-cytokinin interaction may be involved in the dormancy of sycamore seeds.

Hormonal regulation of germination and early seedling development in Acer pseudoplatanus (L.)

Dormancy of intact sycamore (Acer pseudoplatanus) seeds was broken by chilling (5°C) for several weeks in moist conditions. Treatment of unchilled seeds with kinetin induced some germination, but gibberellin was ineffective. This stimulation by kinetin was not suppressed by the added presence of abscisic acid during incubation.The chilling requirement of intact seeds was eliminated by removal of the testa, and the naked embryos developed with no morphological abnormalities. During early growth of isolated embryos in the light, two distinct developmental processes were recognised. One involved initial elongation of the radicle accompanied by geotropic curvature and was stimulated by kinetin but not by gibberellin, while the other involved unrolling of the cotyledons, which was accelerated by gibberellin but much less by kinetin. Abscisic acid strongly suppressed both developmental processes when applied alone, inhibited cotyledon expansion in the presence of gibberellin, but failed to overcome the promotory effects of kinetin on radicle growth. Experiments with CCC indicated that under natural conditions the unrolling of the cotyledons is dependent upon endogenous gibberellin. Radicle growth of isolated embryos was unimpaired by incubation in the dark, but cotyledon expansion of water incubated embryos was poor, and although it was accelerated by gibberellin, the responses in all treatments were slower than in the corresponding light grown samples.It is suggested that endogenous cytokinins are primary factors in the initiation of radicle growth, while gibberellins are important in cotyledon expansion. Abscisic acid appears to have an inhibitory role in both processes, and the interactions of these regulators in the control of germination and development are discussed.