Growth,sugar accumulation,and dark respiration of suspension cell cultures derived from contrasting alfalfa cultivars

Fall dormancy results in decumbent, slow shoot growth of alfalfa (Medicago sativa L.) in autumn and reduced shoot regrowth rates after herbage removal in summer. Although fall dormancy is used to predict alfalfa adaptation, we possess a poor understanding of the biological mechanisms underlying fall dormancy. Our objective was to examine growth and carbohydrate metabolism of suspension cell cultures derived from contrasting alfalfa cultivars that genetically differed in fall dormancy. Suspension cells were grown in B5h media containing 2% sucrose. Cells derived from fall non-dormant plants accumulated sugars more rapidly after transfer to fresh media and to higher concentrations than did cells derived from fall dormant alfalfa cultivars. Dark respiration rates of cells derived from non-dormant plants were similar to those derived from fall dormant plants when growth was limited at low cell sugar concentrations. However, both cell growth and dark respiration rates increased in cells derived from non-dormant cultivars in response to greater cell sugar concentrations. High growth rates of cells derived from rapid growing, fall non-dormant alfalfa cultivars were associated with rapid sugar uptake and higher cell respiration rates when compared to cells derived from dormant alfalfa cultivars.     

Seasonal abundance of the neotropical brown stink bug, Euschistus heros, in overwintering sites, and the breaking of dormancy

The seasonal abundance of the neotropical brown stink bug, Euschistus heros (Heteroptera: Pentatomidae), in overwintering sites in northern Paraná state, Brazil (latitude 23°11 S, longitude 51°11 W) was monitored from September 1994 to August 1995. The breaking of dormancy (oligopause) was studied in the laboratory by comparing the feeding activity and reproduction of adults collected in the field under different physiological conditions (i.e., dormant and non-dormant). No bugs were found in overwintering sites during the summer (December to February) and during early autumn (March). From mid-autumn to winter (April – August), the number of E. heros captured in these sites gradually increased, decreasing thereafter with the start of spring in September. Dormant and non-dormant E. heros taken to the laboratory and maintained at 25 ± 1 °C , 65± 5% r.h., and L14: D10 photoperiod, and given suitable food (soybean pods or seeds), began feeding immediately. The number of stylet sheaths deposited/day on the food was greater for non-dormant than for dormant adults. Feeding activity was greater on immature pods than on mature seeds of soybean. Dormant females placed under suitable biotic and abiotic conditions took ca. 2 weeks to start reproduction, in contrast to non-dormant females, which reproduced immediately.     

Variation between Emex australis populations in seed dormancy/non-dormancy cycles

Abstract Seeds of four Western Australian accessions of Emex australis were stored outside and their germinability tested at 4–6 week intervals for 22 months. Accessions showed cyclical behaviour in germinability, with peaks in autumn/early winter and troughs in spring/summer. There was considerable variation between accessions in dormancy/non-dormancy cycles, but when plants from accessions with contrasting cycles were grown in a common environment, the cycles shown by their seeds were virtually identical. Thus, the parameters of seed dormancy/non-dormancy cycles in E. australis appear to be under environmental control. Only part of an E. australis seed population demonstrated cyclical changes in dormancy status, in contrast to many other annual species whose entire seed populations undergo such changes. Populations also contained individuals which were either continuously dormant or continuously non-dormant following a period of after-ripening. The latter seeds give E. australis the flexibility to recruit opportunistically after summer rainfall events in mediterranean-climate environments.     

The Effects of Temperature and Photoperiod on the Onset of Summer Dormancy in Poa bulbosa L.

Poa bulbosa L. plants became dormant in long days (16 h), whilein short days (8 h) they remained non-dormant for extended periods.Morphologically, the onset of dormancy was expressed by theformation of a true bulb at the base of every tiller, by thecessation of tillering and leaf emergence and, finally, by thedrying-up of the leaves. Low temperature delayed the onset ofdormancy but did not prevent it. This effect of temperaturemay explain the delayed onset of dormancy observed in naturalpopulations under a cool climate at a hilly habitat, comparedto plants growing under a warmer climate, at a lower, coastal-plainhabitat. Dormancy could be induced under short days by pre-exposureof the plants to a limited number of long days. The responsewas proportional to the number of long days given. The adaptivesignificance of the results for plant survival in a Mediterraneanclimate is discussed. Poa bulbosa L., summer dormancy, photoperiod, temperature, leaf emergence, bulbs, tillers     

Clonal dynamics and evolution of dormancy in the leafy hepatic Lophozia silvicola

Dead shoots of colonies of a leafy hepatic species, Lophozia silvicola , are replaced by shoots developing from asexual propagules, the gemmae. Observations of two populations of L. silvicola showed a strong decreasing seasonal trend in germinability of the gemmae. We suggest that the non-germinating gemmae enter dormancy, and that the proportion of gemmae entering dormancy is season-specific. We assume that there are two types of gemmae, dormant and non-dormant and that only the dormant gemmae can survive during winter. Using a stochastic individual-based cellular automaton model, we investigated whether selection on season-specific dormancy fraction would lead to a decreasing proportion of germinating gemmae. Thus the germination schedule is the evolving trait in the model. Parameter estimates for the model were based on data collected from a population of L. silvicola in southern Finland over a three-year study period. In the simulations, the germination schedule shaped by evolutionary change was similar to the observed pattern. Thus the modelling results give support to the dormancy hypothesis. The qualitative pattern of decreasing germinability towards the end of the growing season is robust. Quantitative predictions are influenced by changes in parameters; for example, if winter mortality of shoots increases relative to mortality during the growing season, production of an increased fraction of dormant gemmae is favoured, especially at the end of the season.     

REPRODUCTIVE ATTRITION IN THE RARE CHAPARRAL SHRUB FREMONTODENDRON DECUMBENS LLOYD (STERCULIACEAE)

We examined reproductive attrition in Fremontodendron decumbens to characterize sexual reproduction in this rare California shrub. Reproductive individuals produced an average of 2,900 flower buds in a season, with no significant difference in bud production between two seasons. Because of intense insect predation, <;2% of initiated flower buds became mature fruits. A threefold decrease in predation of flower buds between seasons resulted in an increase in seed output the second season, indicating that seed production was partially predator-limited. Most seeds (97.8%) were dormant due to an impermeable seed coat. Breaking of the coat, mechanically or by heat, allowed high levels of germination. Chamise charate and ash added to the potting medium resulted in the highest level of germination and emergence. Rodents were more important than birds as seed predators, destroying 90% of seeds under parent shrub canopies within 8–10 months. Seeds already integrated into the seed bank were comparatively safe from predation, relative to newly added seeds. If predation was prevented, seeds were long-lived under field conditions (>;80% survived after 5.75 years). Most seedlings produced in unburned chaparral by planting heat-treated seeds in openings between shrubs were destroyed by predators (rodents and insects). All seedlings that escaped predation died during the summer drought. We concluded that sexual reproduction was limited by (in order of importance): 1) lack of fire, 2) predehiscence predation by insects, and 3) postdehiscence predation by rodents. Size distributions from two populations revealed that, despite the apparent absence of sexual reproduction in unbumed chaparral, two unbumed sites contained a large proportion of individuals in small size classes. Excavation of several small individuals demonstrated they were sprouts from the roots of nearby larger shrubs. Because asexual reproduction by rootsprouting circumvents the high attrition of sexual reproductive effort on unbumed sites, rootsprouting may be a significant reproductive strategy of some ‘sprouter’ species in chaparral.     

Dormancy in the Copepoda — an overview

Dormancy affects copepods in their anatomy, physiology, genetics, population biology, community ecology, evolution and local and geographic distribution. It is known from freeliving representatives of three copepod taxa, namely the Harpacticoida, Cyclopoida and Calanoida. Species showing dormancy occur in various realms and habitats, both freshwater and marine, being benthic, planktic or ice-dwelling. Depending on the taxon, dormancy occurs at various times of the year, prevailing in higher and temperate latitudes. Copepod dormancy is expressed in various ontogenetic stages, such as resting eggs, arrested larval development, juvenile and adult encystment, or arrested development of nonencysted copepodids or adults. Ecologically, dormancy is an energy saving trait, allowing the individual to bridge periods of environmental harshness. Adverse environmental conditions could be abiotic (e.g. desiccation, temperature, oxygen availability) or biotic in nature (e.g. food availability, predation). Diapause s. str. is initiated, maintained and terminated by triggering factors (e.g. photoperiod, temperature, chemical cues, population density/physiological factors). The dormant state and emergence patterns directly affect reproduction, population dynamics, community composition, coexistence and distribution of copepods, as well as the phenology of their predators and living food items. Populations having dormancy, in most cases belong to and affect communities of two realms: the water column and the bottom. Dormant stages may provide means for dispersal as well as for staying in special localities. The variability of dormancy permits flexible and complex life histories. Dormancy is subjected to and on the other hand affects copepod evolution.     

GERMINATION ECOPHYSIOLOGY OF HYDROPHYLLUM APPENDICULATUM,A MESIC FOREST BIENNIAL

In north central Kentucky, seeds of the mesic forest biennial Hydrophyllum appendiculatum Michx., are innately dormant at maturity in June. Under natural and simulated seasonal temperature changes, dormancy break occurred in two stages. Root dormancy was broken by high summer temperatures, and shoot dormancy was broken by low winter temperatures. Consequently, roots emerged from seeds during autumn, and cotyledons emerged the following spring. A 90-day warm (30/15 C) stratification treatment broke root dormancy, but the roots emerged only after transfer to lower temperatures. After the warm stratification treatment, roots emerged from 93, 73, 6 and 9% of the seeds incubated at 5, 15/6, 20/10 and 30/15 C (12/12 hr), respectively. Zero, 28, 56 and 84 days of cold (5 C) stratification of seeds with emerged roots resulted in 9, 21, 49 and 82% cotyledon emergence, respectively, at 20/10 C. Thus, H. appendiculatum exhibits a type of morpho-physiological dormancy known as epicotyl dormancy. Although many seeds germinate the first year, others remain dormant and germinate in successive years until the fourth season after ripening.     

Demography of the invasive geophyte Oxalis pes-caprae across a Mediterranean island

BACKGROUND AND AIMS: Success during the early stages of the life-history of alien plants is essential for invasion to occur. The reproductive components of plant invaders have mostly been studied in species reproducing sexually but little is known about invaders that depend exclusively on vegetative reproduction. In this paper, the importance of the different recruitment stages on population growth is quantified and, thus, the invasion potential of the South African annual geophyte Oxalis pes-caprae invading Mediterranean ecosystems is assessed. METHODS: Tests and experiments were conducted across Menorca (Balearic Islands) to analyse the spatial variability of Oxalis pes-caprae reproductive components (i.e. bulb production, bulb bank, bulb predation, bulb mortality, bulb dormancy, bulb germination, plant establishment and survival). KEY RESULTS: Oxalis pes-caprae has a transient bulb bank that remains dormant in the soil during summer. High levels of bulb predation after dispersal, followed by bulb mortality during summer or a failure to germinate in autumn were the most critical factors limiting plant establishment. Bulb germination was high. However, plant establishment and bulb production is constrained by intraspecific competition, but is not affected by soil disturbance. No symptoms of spatial discordance could be found between recruitment stages because the spatial variability of the life cycle was extremely low at all the scales examined (i.e. among populations, habitats and microsites). It was estimated that, on average, 4 % of bulbs can become plants the following year and the field rate of population increase (lambda) to be 0.08. CONCLUSIONS: The results suggest that invasion is constrained by post-dispersal bulb predation, loss of viability of the propagule bank due to summer drought and high intraspecific competition. However, a high spatial concordance between recruitment stages and probably a high propagule pressure due to human and livestock bulb dispersal determine the success of this invader across Menorca Island.     

Role of reactive oxygen species in the regulation of Arabidopsis seed dormancy

Freshly harvested seeds of Arabidopsis thaliana, Columbia (Col) accession were dormant when imbibed at 25°C in the dark. Their dormancy was alleviated by continuous light during imbibition or by 5 weeks of storage at 20°C (after-ripening). We investigated the possible role of reactive oxygen species (ROS) in the regulation of Col seed dormancy. After 24 h of imbibition at 25°C, non-dormant seeds produced more ROS than dormant seeds, and their catalase activity was lower. In situ ROS localization revealed that germination was associated with an accumulation of superoxide and hydrogen peroxide in the radicle. ROS production was temporally and spatially regulated: ROS were first localized within the cytoplasm upon imbibition of non-dormant seeds, then in the nucleus and finally in the cell wall, which suggests that ROS play different roles during germination. Imbibition of dormant and non-dormant seeds in the presence of ROS scavengers or donors, which inhibited or stimulated germination, respectively, confirmed the role of ROS in germination. Freshly harvested seeds of the mutants defective in catalase (cat2-1) and vitamin E (vte1-1) did not display dormancy; however, seeds of the NADPH oxidase mutants (rbohD) were deeply dormant. Expression of a set of genes related to dormancy upon imbibition in the cat2-1 and vet1-1 seeds revealed that their non-dormant phenotype was probably not related to ABA or gibberellin metabolism, but suggested that ROS could trigger germination through gibberellin signaling activation.     

Temperature controls seed germination and dormancy in the European woodland herbaceous perennial Erythronium dens-canis (Liliaceae)

We examined the germination ecology and the temperature requirements for germination of Erythronium dens-canis, under both outdoor and laboratory conditions. E. dens-canis is a spring flowering woodland geophyte widely distributed across Europe. Germination phenology, including embryo development and radicle and cotyledon emergence, were investigated in a natural population growing in Northern Italy. Immediately after harvest, seeds of E. dens-canis were either sown on agar in the laboratory under simulated seasonal temperatures or placed in nylon mesh sachets and buried in the wild. Embryos, undifferentiated at the time of seed dispersal, grew during summer and autumn conditions in the laboratory and in the wild, culminating in radicle emergence in winter when temperatures fell to ≈ 5 °C. Emergence of cotyledons did not occur immediately after radicle emergence, but was delayed until the end of winter. Laboratory experiments showed that temperature is the main factor controlling dormancy and germination, with seeds becoming non-dormant only when given warmth, followed by cold stratification. Unlike seeds of E. dens-canis that germinate in winter, in other Erythronium species radicle emergence occurs in autumn, while in some it is delayed until seeds are transferred from winter to spring conditions. Our results suggest that there is genetic and environmental control of the expression of seed dormancy amongst Erythronium species, which is related to local climate.     

Induction and release of secondary seed dormancy in genetically pure lines of Avena fatua

Induction and release of secondary dormancy in genetically pure dormant (AN-51, Mont 73) and non-dormant (CS-40, SH-430) lines of wild oat ( Avena fatua L.) were studied. These lines differed with regard to the optimal period of anaerobiosis necessary for induction of dormancy, and/or the degree (% of seeds acquiring dormancy) and duration of the dormancy induced. Secondary dormancy could be induced more effectively in the after-ripened seeds of dormant lines than in the non-dormant lines, where only a short-term dormancy could be induced (in 5–7 week-old-seeds). Higher anaerobiosis temperatures were more effective in inducing dormancy in all lines studied. Thus, as with primary dormancy, wild oat biotypes exhibit genetic variability in their secondary dormancy behaviour and factors like temperature can modify the expression of this trait.
The germination stimulants kinetin, isopentenyl adenine, sodium azide, potassium nitrate, ethanol and substituted phthalimides, which break primary dormancy in wild oats, stimulated germination of secondarily dormant seeds (line AN-51). Since these chemicals are structurally diverse, primary and secondary dormancies appear to be similar in part in their regulation.
Salicylhydroxamic acid, an inhibitor of cyanide-insensitive (alternative) respiration, did not inhibit: 1, spontaneous release of secondary dormancy in the line SH-430; and 2, stimulation of germination of secondarily dormant AN-51 seeds by various chemicals (except azide), suggesting that this respiratory pathway is not necessary for the release of induced dormancy.     

Incidence of diapause varies among populations of <Emphasis Type="Italic">Daphnia pulicaria</Emphasis>

Dormancy is a common way in which organisms survive environmental conditions that would be lethal to the active individual. However, while dormant, individuals forgo reproduction. Hence theory suggests an optimal time in which to enter dormancy, depending on risks associated with both remaining active and entering dormancy. When these relative risks differ among habitats, dormancy strategies are predicted to vary as well. For freshwater zooplankton, it has been suggested that sensitivity to the cues that initiate dormancy should be selected against when females have the opportunity to remain in the water column year round. We tested this prediction with 12 populations of lake-dwelling Daphnia pulicaria (Crustacea: Cladocera). Differences among lakes in basin morphometry, predators and resources create a gradient of risk for Daphnia in the water column. Some populations persist in high numbers year round while others are abundant only in spring. We used this difference in persistence ability as an estimate of risk in the water-column. For 3 years of field sampling we found consistent differences among the lake populations in the incidence of dormancy. In some populations, only a small fraction of females switched to producing dormant eggs each year whereas in others the majority of eggs produced in the late spring were dormant. In general, populations that experienced predictably low abundances in the active form exhibited higher incidence of dormancy than did populations that persisted in high abundance year round, but there were exceptions. Our results confirm that the incidence of dormancy varies considerably among populations in a fashion consistent with general theory, but suggest that persistence in the water column is not the sole predictor of the diapause strategy found in any particular lake.     

Effects of primary seed dormancy on lifetime fitness of Arabidopsis thaliana in the field

Background and AimsSeed dormancy determines the environmental niche of plants in seasonal environments, and has consequences for plant performance that potentially go far beyond the seed and seedling stages. In this study, we examined the cascading effects of seed dormancy on the expression of subsequent life-history traits and fitness in the annual herb Arabidopsis thaliana.MethodsWe planted seeds of >200 recombinant inbred lines (RILs) derived from a cross between two locally adapted populations (Italy and Sweden), and both parental genotypes at the native site of the Swedish population in three consecutive years. We quantified the relationship between primary seed dormancy and the expression of subsequent life-history traits and fitness in the RIL population with path analysis. To examine the effects of differences in dormancy on the relative fitness of the two parental genotypes, we planted dormant seeds during the seed dispersal period and non-dormant seeds during the germination period of the local population.Key ResultsIn the RIL population, strong primary dormancy was associated with high seedling survival, but with low adult survival and fecundity, and path analysis indicated that this could be explained by effects on germination timing, rosette size and flowering start. The relationship between primary seed dormancy and germination proportion varied among years, and this was associated with differences in seasonal changes in soil moisture. The planting of dormant and non-dormant seeds indicated that the lower primary dormancy of the local Swedish genotype contributed to its higher germination proportion in two years and to its higher fecundity in one year.ConclusionsOur results show that seed dormancy affects trait expression and fitness components across the life cycle, and suggest that among-year variation in the incidence of drought during the germination period should be considered when predicting the consequences of climatic change for population growth and evolution.     

Dormancy and enzyme levels in seeds of wild oats

Nine enzymes were compared in dry and steeped mature dormant and non-dormant seeds of wild oats. In dry seeds only glutamate-pyruvate transaminase and phosphoglycerate kinase were greater in non-dormant seeds. In steeped non-dormant seeds glucose-6-phosphate dehydrogenase activity doubled while the enzyme declined sharply in dormant seeds. Increases in isocitrate dehydrogenase, glutamate-oxaloacetate transaminase and acid phosphatase in non-dormant seeds, during steeping, are consistent with the hypothesis that the pentose phosphate and glycolysis-tricarboxylic acid pathways are involved in the control of dormancy of wild oat seed.     

A combined physical and physiological dormancy controls seasonal seedling emergence of Geranium robertianum

Temperate forest herbs with seeds exhibiting both a physical and a physiological dormancy mechanism are rare, and knowledge on the factors regulating germination of these species is fragmentary. The biennial Geranium robertianum L. grows mainly in temperate woodlands, but can also be found in exposed habitats. Seedlings of G. robertianum are known to emerge from spring until autumn, but little is known about the environmental factors regulating germination. In this study, phenology of seedling emergence and of physical dormancy loss was examined for seeds buried at shaded or sunny exposed locations. The role of temperature in regulating dormancy and germination was analysed by incubating seeds in temperature sequences simulating temperatures that seeds experience in nature. The results indicate that most seeds of G. robertianum buried in sunny conditions germinate immediately after physical dormancy loss in summer. Seeds buried in shaded conditions also lose physical dormancy mainly during summer, but remain physiologically dormant and do not germinate until late winter or early spring. Besides physical dormancy, seeds of G. robertianum also initially have a high level of physiological dormancy, which is reduced during dry storage. Physiological dormancy is reduced through chilling in winter, thus enabling the seeds to germinate at low temperatures. We conclude that a complex combination of physical and physiological dormancy ensures that G. robertianum seeds germinate in summer at exposed sites and in early spring at shaded sites.     

Clonal diversity and turnover in an overwintering Daphnia pulex population,and the effect of fish predation

相似文献   

THE CHEMICAL REGULATION OF THE DORMANCY PHASES OF BUD DEVELOPMENT

literature pertaining to the development and regulation of dormancy in the buds of woody species is reviewed and interpreted as follows. Morphological observations, the effects of environmental factors, and other evidence support the concept that bud dormancy involves a cycle of 3 separate phases of development. Beginning at the developmental pattern of spring, the 3 phases are: (1) dormancy development leading to the dormant state; (2) release from dormancy leading to the non-dormant state; and (3) the initiation of spring burst leading again to spring development. The regulation of dormancy is, therefore, discussed in terms of the regulation of development of the apex within each phase and the regulation of transitions between phases. The principal existing theory of dormancy regulation implies that dormancy consists, in total, of merely the inhibition of spring development, and that regulation involves first the accumulation of an inhibitor then its disappearance. The conceptual basis of this inhibitor theory is argued to be inadequate as is the experimental evidence for the existence of a specific inhibitor and for a correlation between its concentration and dormancy induction or release. There is little direct evidence on the mechanism of the regulation of bud development within any developmental phase. Circumstantial evidence suggests the developmental patterns arise from chemical patterns resulting from the interactions of classes of growth regulator such as auxin, kinin, and gibberellin. Some evidence exists concerning the regulation of the transitions between the phases of dormancy. A substance has recently been detected which may be a hormone regulating the initiation of dormancy development. The production of this substance may be photoperiodically determined. A role for gibberellins in the regulation of dormancy release has been postulated.