Accumulation of sugars during the onset and development of desiccation tolerance in immature seeds of Norway maple (Acer platanoides L.) stored moist

2000 ◽  
Vol 10 (2) ◽  
pp. 147-152 ◽  
Author(s):  
T.D. Hong ◽  
A. Gedebo ◽  
R.H. Ellis

AbstractThe viability of Norway maple seeds collected 21 d before mass maturity (68%moisture content, wet basis) and at mass maturity (56% moisture content) was reduced from 52–85% to 0–7% if dried rapidly (at 10–12% r.h. and 15–17°C for 3 d, then 3 d over silica gel) to 4–5% moisture content. Moist storage of the fruits at 15°C improved the ability of the seeds to tolerate rapid desiccation considerably: 10 and 21 d of moist storage enabled seeds collected at mass maturity or 21 d earlier, respectively, to attain maximum desiccation tolerance to 4–5% moisture content. Moist storage and/or subsequent desiccation affected stachyose, sucrose, and to a lesser extent raffinose, concentrations. The oligosaccharide:total sugar ratio showed a similar pattern in relation to ability to germinate after desiccation to 4–5% moisture content among seeds collected on both dates: desiccation tolerance developed from nil to maximal in these seed populations between threshold oligosaccharide:total sugar values of just less than 0.3 and about 0.4.

1992 ◽  
Vol 2 (3) ◽  
pp. 169-172 ◽  
Author(s):  
T. D. Hong ◽  
R. H. Ellis

AbstractNorway maple (Acer platanoides L.) seeds were harvested at different stages of seed development and maturation in 1989–91. As maturation drying progressed, the seed populations showed increasing desiccation tolerance: at 67–69% moisture content, no seeds survived desiccation below 10% moisture content; maturation drying to 55–57% moisture content (values corresponding with the end of the seed-filling phase) improved desiccation tolerance, but nevertheless most seeds were unable to withstand desiccation to 5–7% moisture content; further maturation drying to 27–28% moisture content enabled the seeds to survive considerable desiccation, no loss in viability occurring in seeds dried to 3% moisture content. This considerable improvement in desiccation tolerance after the end of the seed-filling phase was correlated (P<0.05) with the progress of maturation drying and may be associated with the increase in the potential longevity of seeds of other species that occurs during seed development subsequent to seed filling.


1991 ◽  
Vol 1 (3) ◽  
pp. 149-162 ◽  
Author(s):  
J. B. Dickie ◽  
K. May ◽  
S. V. A. Morris ◽  
S. E. Titley

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.


1997 ◽  
Vol 7 (1) ◽  
pp. 41-46 ◽  
Author(s):  
T. D. Hong ◽  
R. H. Ellis

AbstractThe viability of Norway maple seeds harvested at mass maturity (57.3% moisture content) was reduced from 100% to only 38% if dried rapidly (at 15% RH and 15°C for 3 days) to 4.7% moisture content. In contrast, slow drying for 32 days (the optimum duration of several investigated) to 29.9% moisture content enabled 93% of the seeds to survive subsequent rapid desiccation to 3.5% moisture content. This is similar to the 95% viability shown by seeds harvested 40 days after mass maturity and then dried rapidly to 4.4% moisture content. However, fruits or seeds harvested at mass maturity and then held moist for 21 days also showed 94 and 91% viability after subsequent rapid desiccation to 3.8 and 3.3% moisture content, respectively. Thus a post-ovule-abscission programme is required before Norway maple seeds are able to tolerate rapid enforced desiccation to low moisture contents, but loss in moisture during this period is not essential to the development of desiccation tolerance.


1990 ◽  
Vol 8 (1) ◽  
pp. 22-25
Author(s):  
Paul Murakami ◽  
Tony H.H. Chen ◽  
Leslie H. Fuchigami

Abstract Nurserymen consider Washington hawthorn (Crategus phaenopyrum Med.) sensitive and Norway maple (Acer platanoides L.) tolerant to postharvest practices. The desiccation tolerance, cold hardiness and water potential at various growth stages were monitored on field-grown Washington hawthorn and Norway maple. There were no differences between these two species in the rate of water loss in the root, shoot or whole plants. Hawthorn, however, was more sensitive to desiccation stress than maple throughout all growth stages. The roots lost water at a faster rate than the stems in both species. Hawthorn plants acquired rest and cold hardened later in the fall and attained less dormancy and less freezing tolerance than did maple.


2000 ◽  
Vol 10 (3) ◽  
pp. 329-339 ◽  
Author(s):  
Françoise Corbineau ◽  
Mari Ange Picard ◽  
Jean-Albert Fougereux ◽  
Fabienne Ladonne ◽  
Daniel Côme

Germination and carbohydrate metabolism were studied in fresh developing pea (Pisum sativum L., cv Baccara) seeds and after artificial drying at 25°C and various relative humidities (20, 75 and 99% RH) to investigate whether the occurrence of desiccation tolerance was related to sucrose, raffinose and stachyose contents. Seeds became completely tolerant to fast drying at 25°C and 20% RH a few days after the end of reserve accumulation, i.e. when their moisture content dropped to approx. 50% (fresh weight basis). This acquisition of desiccation tolerance was associated with an accumulation of raffinose and stachyose, the latter being more abundant in the embryonic axis than in the cotyledons. The (raffinose+stachyose)/sucrose ratio increased during seed development and reached 1.1 in the axis and 0.2 in the cotyledons just before the onset of desiccation tolerance. When the natural acquisition of desiccation tolerance occurred on the mother plant, artificial drying of isolated seeds induced an increase in oligosaccharide content in the cotyledons. Immature seeds, the moisture content of which was higher than about 60% (fresh weight basis), did not tolerate fast drying (25°C and 20 or 75% RH). Such drying did not result in the synthesis of stachyose and induced an increase in electrolyte leakage, a decrease in the ability of seeds to convert 1-aminocyclopropane 1-carboxylic acid (ACC) to ethylene and an increase in ethane synthesis, thus indicating a deterioration of cell membrane properties and lipid peroxidation. In contrast, immature seeds tolerated drying either in the pods or at 25°C and 99% RH, and such drying induced a decrease in sucrose content, an increase in oligosaccharide content and a (raffinose+stachyose)/sucrose ratio higher than around 1. Soluble sugar contents of dried immature seeds depended on the conditions of dehydration. In cotyledons, the (raffinose+stachyose)/sucrose ratio reached 0.61 when seeds were dried at 25°C and 99% RH, whereas it was as low as 0.15 when drying was performed at 25°C and 20% RH. All the results obtained are consistent with the concept that oligosaccharides may well be involved in the protection of membranes during dehydration.


2014 ◽  
Vol 26 (3-4) ◽  
pp. 42-61
Author(s):  
O. G. Lucyshyn ◽  
I. K. Teslenko

The recent ecological situation of Kyiv megalopolis has a special specific of environment technogenic pollution as a chemical features and content of polluting phytotoxicants. During 2007–2012, our observation revealed what the most dangerous factors which have harm impact on the street woody plants are the huge concentration of phytotoxic elements (Na+, Cl-, Pb2+, Cd2+). Nowadays, the technogenic impact on the megalopolyisis surrounding comes to the dangerous, even, catastrophic level. The main reason of total and chloral necrose of leaves, the summer defoliation of crown and major tree's death is the over pollution of the soil and plant's phytomass by phytotoxic elements, the concentration of which by standards evaluation and by trees reactions are critical and exists at the level of adaptation possibility and survival. The main sources of Pb2+ and Cd2+ ions are transport outcomes (> 90 % of total technogenic pollution). The increasing of Pb2+ and Cd2+ in the soil is depended from intensivity of transport outcomes, using of ethylated petrol, and location of trees along roads as well as from the trees species. Continuously increasing of number of cars at the city streets is accompanying with similar increasing of ions concentration. Thus, in the soil around root system of street woody plants, depending from their location along roads, the concentration of Pb2+ (moving form) is between 41,7 (I. Kudri str.) and 102,6 mg\kg of soil (Nauki avenue). It exceeds the maximum permissible concentration (MPC), which is 20,8–51,3 mg\kg of soil. Next, for Norway maple (Acer platanoides) the concentration of Pb2+ in the soil varies from 41,7 to 80,5 mg / kg of soil in the area of the root system and it is around 20,8–40,2 MPC. In the leaves of this tree it is 7,83–13,5 mg / kg of dry mass (MPC is 15,8–27,0). For the horse chestnut (Aedculus hippocastanum) at the Nauka avenue, the concentration of plumbum in the root is 13,4 mg / kg (MPC is 26,8), in the cortex – 17,7 mg / kg (MPC is 35,4), in leaves – 8,21 mg / kg (MPC is 16,4), which by the normative evaluation are the critical concentrations. The source of Na+ and Cl-, which is a new factor for Kyiv megalopolis, is irregular load of high concentrations of industrial salt NaCl into the environment, as a way against black ice in winter time, where the Na+ ions ( mobile form) is in the high concentrations in leaves (0,76 % for Norway maple (Acer platanoides) on the I. Kudri str., 1,28 % – small-leaved linden (Tilia cordata) at the 40-richya Zhovtnya ave, 2,0 % – horse chestnut (Aedculus hippocastanum) at the Nauki ave), those are exceeded the concentration of the element comparing to the control test object, respectively, in 10,6, 12,8 and 5,0 times. Na+ ions are an aggressive phytotoxins and the main factor of leaves necrose of tree crown (within 70–100 % necrosis leaves in the crown). Degradation and total reduction of the specific weight of plants in the megalopolis environment are decrease the cleaning role of the street tree plants, which are the main alive filters for soil and air cleaning, as well as the main bioaccumulators and detoxicants of harm substances of anthropogenic pollution. Species adaptive specificity is revealed at the bioaccumulation level and the selective locality of phytotoxic elements (Na+, Cl-, Pb2+, Cd2+, agile form) in technourbanhabitats-pic conditions, there dominated bioaccumulation and localization of Na+ ions by trees assimilative system is caused the adaptive orientation of endogenic and intraspecific variability of phytoindicative morphophysiologic features of plants functional condition under the stressing factors. This also is defined the sensitivity of small-leaved linden (Tilia cordata Mill.), norway maple (Acer platanoides L.) and horse chestnut (Aesculus hippocastanum L.) to the big concentration of potassium as the most danger one for the plant survival. The biggest accumulation of Na+ ions at the roots of Lombardy poplar (Populus pyramidalis Roz.), Bolle's poplar (Populus bolleana Lauche) and sugar maple (Acer saccharinum L.) is lead to a higher resistance of their assimilation system. At the technourbohabitate-pic conditions, the level of realization of ontogenetic and phylogenetic adaptive capacity of the sensitive species of trees is harmfully low (21,3–44,3 %). It is at the level of survival/death of plants. The street Lombardy poplar, Bolle's poplar and sugar maple, despite of more higher level of their adaptation (68,4–87,7 %), still also can't fully adapt to the critical levels of technogenic pollution of megalopolis environment. 


Antioxidants ◽  
2020 ◽  
Vol 9 (5) ◽  
pp. 391 ◽  
Author(s):  
Natalia Wojciechowska ◽  
Shirin Alipour ◽  
Ewelina Stolarska ◽  
Karolina Bilska ◽  
Pascal Rey ◽  
...  

Norway maple and sycamore produce desiccation-tolerant (orthodox) and desiccation-sensitive (recalcitrant) seeds, respectively. Drying affects reduction and oxidation (redox) status in seeds. Oxidation of methionine to methionine sulfoxide (MetO) and reduction via methionine sulfoxide reductases (Msrs) have never been investigated in relation to seed desiccation tolerance. MetO levels and the abundance of Msrs were investigated in relation to levels of reactive oxygen species (ROS) such as hydrogen peroxide, superoxide anion radical and hydroxyl radical (•OH), and the levels of ascorbate and glutathione redox couples in gradually dried seeds. Peptide-bound MetO levels were positively correlated with ROS concentrations in the orthodox seeds. In particular, •OH affected MetO levels as well as the abundance of MsrB2 solely in the embryonic axes of Norway maple seeds. In this species, MsrB2 was present in oxidized and reduced forms, and the latter was favored by reduced glutathione and ascorbic acid. In contrast, sycamore seeds accumulated higher ROS levels. Additionally, MsrB2 was oxidized in sycamore throughout dehydration. In this context, the three elements •OH level, MetO content and MsrB2 abundance, linked together uniquely to Norway maple seeds, might be considered important players of the redox network associated with desiccation tolerance.


2007 ◽  
Vol 55 (6) ◽  
pp. 618 ◽  
Author(s):  
Kim N. Hamilton ◽  
Sarah E. Ashmore ◽  
Rod A. Drew ◽  
Hugh W. Pritchard

Combinational traits of seed size and seed-coat hardness in Citrus garrawayi (F.M.Bailey) (syn. of Microcitrus garrowayi) were investigated as markers for estimation of seed morphological and physiological maturity. Seed size (length) and coat hardness correlated well with changes in seed coat and embryo morphological development, dry-weight accumulation, decreases in moisture content and a significant increase in germinability. Seed moisture content decreased from 82 ± 1% in immature seeds to 40 ± 1% at seed maturation. The outer integument of immature seeds consisted of thin-walled epidermal fibres from which outgrowths of emerging protrusions were observed. In comparison, mature seed coats were characterised by the thickening of the cell walls of the epidermal fibres from which arose numerous protrusions covered by an extensive mucilage layer. Immature seeds, with incomplete embryo and seed-coat histodiffereniation, had a low mean germination percentage of 4 ± 4%. Premature seeds, with a differentiated embryonic axis, were capable of much higher levels of germination (51 ± 10%) before the attainment of mass maturity. Mature seeds, with the most well differentiated embryonic axis and maximum mean dry weight, had the significantly highest level of germination (88 ± 3%).


1958 ◽  
Vol 90 (9) ◽  
pp. 538-540 ◽  
Author(s):  
C. C. Smith

The fall cankerworm, Alsophila pometaria (Harr.), and the winter moth, Operophtera brumata (Linn.), both feed to a great extent on the same tree species and prefer apple, Malus spp., red oak, Quercus rubra L., basswood, Tilia spp., white elm, Ulmus americana L., and Norway maple, Acer platanoides L. They also have similar life-histories and habits (Smith 1950 and 1953). Both lay their eggs on the trees in the fall and overwinter in this stage. The eggs hatch about the same time and the larvae of (both species mature about the third week in June. They drop to the ground and form cocoons at a depth of about an inch. The adults emerge about the same time, commencing usually during the last week in October and continuing until early December or until the ground freezes.


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