菹草石芽大小和贮藏温度对萌发及幼苗生长的影响

通过萌发实验探讨了菹草石芽重量和贮藏温度对石芽萌发及幼苗生长的影响。结果表明：成熟的菹草石芽大小不一,按鲜重划分重量等级,各等级石芽数量占总数量的百分比差异很大,重量中等的石芽数量占到80%以上;重量对石芽最终萌发率没有影响,但重量小的石芽萌发时间较早,重量大的石芽虽然萌发较晚但是最终萌生的幼苗数目较多。石芽重量和萌发结束时幼苗数目之间呈显著的线性正相关(p＜0.05);连续去苗过程中,重量大的石芽萌发率和萌发幼苗数保持较高水平;经过贮藏的石芽与未经贮藏的石芽相比,萌发快且萌发整齐。经过15℃贮藏的石芽萌发最早,高温(25℃)和低温(4℃)贮藏均会使石芽最终萌发出的幼苗数目减少,3种温度下贮藏的石芽最终萌发率和幼苗长度无显著差异。     

Photophysiology of turion germination inSpirodela polyrhiza (L.)Schleiden. The cause of germination inhibition by overcrowding

Red-light-induced (via phytochrome) germination decreased with increasing numbers of turions per germination flask (overcrowding). Three hypotheses concerning the mechanism of this germination inhibition were tested, related to abscisic acid, ethylene, and oxygen deficiency: (i) Although abscisic acid is a powerful inhibitor of turion germination it had to be excluded as a cause, because abscisic acid was not secreted from turions into the nutrient solution, (ii) Ethylene (ethrel) strongly inhibited growth of newly formed sprouts, but germination response itself was not inhibited, (iii) Germination inhibition did not appear if short light pulses were substituted by continuous irradiation. It reappeared in the presence of the photosynthesis inhibitor 3-(3, 4-dichlorophenyl)-l, 1-dimethylurea, but it was not observed in aerated nutrient solutions, or when Petri dishes instead of Erlenmeyer flasks were used. Decreased oxygen concentrations in the nutrient solution were produced by turion respiration. Consequently, anaerobiosis within the nutrient solution caused by turion respiration was the reason for germination inhibition by overcrowding.     

Life cycle and growth ofPotamogeton crispus L. in a shallow pond,ojaga-ike

The life cycle and growth ofPotamogeton crispus L. were studied in a shallow pond, Ojaga-ike. With respect to the shoot elongation and seed and turion formations, the life cycle of this plant in the pond could be divided into following five stages: germination, inactive growth, active growth, reproductive and dormant stages. It was suggested that the plant showed these successive stages depending mainly upon water temperature. The turions germinated on the bottom in autumn when the water temperature fell below ca. 20 C. The plant showed hardly any growth during winter (December—early March) when the temperature was below 10 C. In the spring when the bottom water temperature rose to above 10 C (mid-March), the plant started to grow again and the shoot elongated rapidly at the rate of 4.2 cm day⁻¹ until the shoot apex reached the pond surface in late April. Both the increment of node number and the internodal elongation were associated with this rapid shoot growth. On 10 May (last sampling date), the mean values of shoot length, internodal length and the number of nodes estimated for 10 predominant plants were 238.2±5.6 cm, 7.1±0.8 cm and 34.9±4.0 cm, respectively. The turion formation and flowering occurred during the period from mid-April to mid-May when the surface water temperature ranged 19 and 22 C. The dry weight of a plant reached the maximum mean value of 1180 mg on 10 May. At its peak biomass, an individual plant produced 1–10 turions (5.5 on average) of which the mean individual turion dry weight was 53.2 mg. The turion dry weight accounted for ca. 42% of the total plant biomass m⁻² at that time.     

TURION FORMATION AND GERMINATION IN SPIRODELA POLYRHIZA

Three clones of Spirodela polyrhiza L. (Schleid.) formed dormant bodies called turions. A clone from Puerto Rico did not form turions under all conditions tried. In those clones producing turions, formation was stimulated by the addition of sucrose (10–50 mM) to the nutrient solution. Increased levels of Ca(NO₃)₂ plus sucrose stimulated turion production. In the absence of NO₃^–, Ca⁺⁺ was more effective than K⁺ in stimulating turion formation. Turion buoyancy was not light dependent, nor was it promoted by sucrose. Normal turions required light for germination, whereas sucrose-induced turions germinated in the dark. Dark germination was not promoted by either Ca⁺⁺ or K⁺. Sucrose stimulation of turion formation and subsequent promotion of dark germination was attributed to metabolic rather than osmotic effects. One hundred mM sucrose concentrations inhibited turion buoyancy and germination. Turions formed one primary abscission layer which separated them from the stolon and the mother frond. Subepidermal idioblasts appeared to seal the stolon stump after separation.     

Cell wall polysaccharidase activities and growth processes: a possible relationship

The turions of Potamogeton crispus L. develop in early summer and function in propagation and dispersal. Under natural conditions during longday periods, an average minimum air temperature of more than 12°C was found to be important for turion formation. Experiments with controlled environments indicate that both temperature and photoperiod regulate turion formation. Turions can be induced at 13°C or above but not at 8 or 10°C. At a temperature range of 13–24°C turions form in both 12- and 16-h days, but not in 8-h days. By increasing temperature from 24 to 30 or 35°C turions can be induced under 8-h days. Light intensity was found to be important in the formation of turions.     

Low‐molecular weight carbohydrates modulate dormancy and are required for post‐germination growth in turions of Spirodela polyrhiza

The aquatic duckweed Spirodela polyrhiza propagates itself vegetatively by forming turions – bud‐like perennation organs – in the autumn, which spend the winter on the bottom of ponds and then germinate in the following spring and proliferate on the water surface. Newly formed turions usually require a period of cold after‐ripening and light to germinate effectively, but an ample supply of exogenous sugar can lead to germination even in the dark and independent of after‐ripening. The results of the present study indicate that the availability of readily metabolised carbohydrates is a determining factor for turion germination. Freshly harvested turions do not contain soluble, low‐molecular weight carbohydrates at a level sufficient to allow germination to take place, but after‐ripened turions do. Augmentation of the soluble carbohydrate content during after‐ripening derives from gradual breakdown of reserve starch of the turions. The long time required for any germination to be observed in turions incubated in darkness and the limited frequency of germination in the dark (about 50% of turion population), even with an ample external sugar, supply emphasise that both after‐ripening and light are essential for ensuring rapid germination and subsequent frond proliferation at an ecologically appropriate time. The carbohydrate supply required for rapid proliferation of the fronds produced at germination is provided by the rapid light‐induced breakdown of turion reserve starch.     

Growth and turion formation of Potamogeton crispus in response to different phosphorus concentrations in water

The vegetative growth and turion formation of Potamogeton crispus, a submersed aquatic macrophyte, was investigated under a range of phosphorus (P) concentrations (0.025, 0.25, 2.5 and 25 mg P L^?1) in the ambient water free of algae, aiming to identify the responses of submersed aquatic macrophytes to nutrient enrichment, a common eutrophication problem in China and worldwide. Plant growth was not affected by different P concentrations in terms of biomass accumulation of stems and leaves. However, the contents of chlorophyll a and starch in plants decreased with increasing water P levels, whereas chlorophyll b and carotenoids declined with P level ranging from 0.025 to 2.5 mg P L^?1. The soluble sugar content decreased when water P concentration increased up to 2.5 mg L^?1. The P content in plants increased with increasing water P levels, whereas plant N content decreased and soluble protein increased when water P concentration increased over 0.25 mg L^?1, implying that P. crispus may have modified its metabolism to adapt to water P availability. When P concentration increased to 25 mg L^?1, the number and dry matter production of turions per plant decreased significantly. Meanwhile, there was a significant reduction in turion weight and the accumulations of soluble sugar and starch in turion, when water P concentration was over 0.25 mg L^?1. The results suggest that turion formation in P. crispus is sensitive to P concentration in the ambient water, and high P levels may lead to decreases in P. crispus populations due to the decline in turion production.     

Community collocation of four submerged macrophytes on two kinds of sediments in Lake Taihu, China

To explore a method for rapid restoration and artificial regulation of submerged macrophytes in large-scale restoration of eutrophic lakes, the succession and the biodiversity changes of four communities composed of four native, common submerged macrophytes, Hydrilla verticillata, Potamogeton malaianus, Vallisneria spiralis and Najas marina, on two kinds of sediments were investigated. Under low light intensity (reduced by 99%), the plant biomass changed with seasonal changes, plant competition, and environmental stress. The competitive capability for light differed in the four species due to different shoot height and tiller number. After 405 days of transplantation, H. verticillata became dominant in all communities. The biomass of H. verticillata, with strong ability to endure low water light environment, accounted for more than 90% of the total community biomass, and P. malaianus had only weak growth, while V. spiralis and N. marina almost disappeared. Based on livability and biomass of submerged macrophytes on two sediment types, brown clay sediment appeared to be more favorable for the settlement of the plants, while fertile sludge sediment was suitable for vegetative growth. In conclusion, the improvement of habitats and the selection of appropriate plant species are of the greatest importance for ecological restoration of the aquatic ecosystem.     

On the germination of turions and the life cycle of Potamogeton trichoides Cham. et Schld.

The life cycle of P. trichoides Cham. et Schld. has been studied in a pond near Nijmegen (The Netherlands); the germination of its turions has been studied in relation to temperature, cold induction (stratification) and light dependency. The species shows a summer-green annual life cycle, surviving the winter period by means of turions. Timing of turion germination appears to be well regulated by the water temperature, but light was also effective.     

Stay dormant or escape sprouting? Turion buoyancy and sprouting abilities of the submerged macrophyte Potamogeton crispus L.

The ability of asexual propagules to disperse is an important ecological determinant of the spread and establishment of many aquatic species. However, few previous studies have addressed the relationship between the asexual propagule buoyancy and sprouting abilities in submerged macrophytes. For this reason, turions of Potamogeton crispus samples were collected from Lake Liangzi, and an incubator sprouting experiment was conducted. Our results revealed that the floating turions showed higher sprouting rates than that of sinking turions, indicating the former ones are possibly with high levels of primary metabolites. The higher N and P concentrations in the floating turions caused lower C:N, C:P, and N:P ratios in these turions compared with sinking turions, which confirmed the activation of floating turions. The free amino acid and soluble carbohydrate concentrations were also higher in floating turions than those in sinking turions. Our results also revealed that turion leaf porosity rather than starch concentration may determine the density of P. crispus turions. This study makes a contribution to our understanding of how the internal characteristics of turions can (at least partly) determine dispersal outcomes and offers new insights into the dispersal and sprouting of asexual propagules of submerged macrophytes.     

Biomanipulation-induced reduction of sediment phosphorus release in a tropical shallow lake

Biomanipulation via fish regulation combined with submerged plant introduction is an effective measure to restore eutrophic shallow lakes. Improved water quality and clarity promote growth of benthic algae, which with submerged plants may limit sediment phosphorus (P) release, thereby reinforce lake recovery. Our study sought to evaluate the effect of such a biomanipulation on water quality, benthic algal development and sediment P release in a shallow, tropical lake by (1) comparing porewater and lake water quality, light intensity and benthic algal development in restored and unrestored sections; (2) conducting a ³²P radiotracer experiment to track P release from sediment cores sampled from both sections. The biomanipulation led to lower total P, total dissolved P, and soluble reactive P concentrations in lake water, lower phytoplankton biomass, and increased light intensity at sediment surface, stimulating benthic algal development. Moreover, sediment ³²P release was lower in the restored than unrestored section. Concurrently, dissolved oxygen levels in upper layers of the sediment cores were higher in the restored section. Our study indicates that the biomanipulation improved water quality and enhanced growth of benthic algae, thereby reducing sediment P release, which may be one of the main mechanisms to create successful restoration.     

Co‐action of temperature and phosphate in inducing turion formation in Spirodela polyrhiza (Great duckweed)*

Increased phosphate concentration, higher temperature and addition of glucose all increased the number of fronds and turions of the duckweed Spirodela polyrhiza formed under in vitro conditions. Increasing the number of turions by increasing the plant biomass does not mean that the developmental process (switch of the programme of the primordia from vegetative fronds toward resting turions) has been specifically influenced. The specific turion yield (STY; number of turions formed by one frond) and the time of onset of turion formation have been used as more specific measures of turion induction. At more than 30 µm initial phosphate the STY was increased by lower temperature (15 °C) and became independent of the phosphate concentration. Between 10 and 30 µm and at higher temperatures (25 °C) the STY was increased by lower phosphate levels. The stimulatory effect of lower temperature was more pronounced than that of lower phosphate concentrations. Decreased phosphate concentration highly accelerated the formation of the first turions. The influence of low temperature was small at lower phosphate concentration but became dominant at higher concentrations (especially in autotrophic cultures). Low phosphate levels (e.g. 10 µm ) and low temperatures (e.g. 15 °C) both represent specific turion‐inducing factors having significant interactive effects. In S. polyrhiza, these signals may replace the interactive effects of photoperiods and low temperature known from other hydrophytes in turion induction under natural conditions.     

Changes in vectors of endogenously generated ion currents in light-induced germination of turions of Spirodela polyrrhiza

Nondormant turions of Spirodela polyrhiza (L.) Schleiden were utilized to investigate endogenous ion currents in light-induced germination and early growing processes of higher plants. A small outward current was detected at the ventral side of the turions near the pocket containing the most developed sprout primordium. After a light pulse, the direction of the endogenous current changed from outward to inward. These ion currents are most likely conditioned by unspecific diffusion of cations (probably H+) inside the cell. Three-day-old sprouts of Spirodela showed the highest inward current near the sprout base which decreases toward its edge. Newly formed sprouts demonstrated a strong gravity effect (bending), which was preceded by a lowering of the Z-component of vectors close to the sprout base after a change of the turion fixation.     

梁子湖苦草繁殖体的分布及其萌发初步研究

苦草鳞茎(冬芽)在梁子湖的垂直分布深度与其重量呈显著正相关,而重量也与鳞茎芽数显著相关 (P<0.05).埋藏深度、水分状况和鳞茎本身的大小都显著影响鳞茎的出土能力.去除第一位芽和切碎鳞茎后促进了其余芽的萌发;上年产生的未萌发的鳞茎在条件适宜的时候也可以很好的萌发,这些可能成为苦草在鳞茎被牧食后,维持种群数量的有效对策.沙质底比泥质底更有利于苦草种子的萌发,但在没有扰动的情况下,幼苗的定植能力在两种基质中没有显著差异.       

Dormancy, Turion Formation, and Germination by Different Clones of Spirodela polyrrhiza

Some clones of Spirodela polyrrhiza form dormant bodies called turions which require several weeks of chilling treatment before they proceed to renew growth and develop into vegetative fronds. The individual fronds of Spirodela are less than 5 mm long and can be grown aseptically in liquid culture. Turion formation and germination can serve as a bioassay for the various compounds involved in dormancy development.

Turion formation can be induced by manipulation of light intensity during the day, photoperiod, night temperature, day temperature, and concentration of nitrate in the culture medium. Different clones of Spirodela from northeastern United States, Puerto Rico, and Argentina had different requirements for turion formation. The clones from Argentina and Puerto Rico did not form turions under any of the experimental conditions imposed. Turions of some clones required chilling treatments for renewed vegetative growth while others did not. Both gibberellic acid and long photoperiods were required to bypass the chilling requirements of some clones, but not others.

     

Dormancy and germination in axillary turions ofHydrilla verticillata

Effects of environmental conditions and growth regulators on release from dormoncy of axillary turions inHydrilla verticillata were investigated. Coll treatment at 2 C for 33 days produced the most complete release from dormancy. One week of 2 C treatment was sufficient for the germination; however, longer cold periods produced more rapid growth in shoot or root lengths as well as a shorter lag time for germination. Dormancy in turions could be broken by a photoperiod of 16 hr but not by on of 8 or 12 hr, nor by continuous lighting. When a cold treatment was applied turions grew out in response to all of the photoperiodic conditions. Red and far-red irradiation during the incubation after a cold treatment promoted gremination; blue and green light markedly inhibited the germination. At 10⁻⁴ and 10⁻⁵ M, gibberellic acid broke dormancy of non-cold treated turions, but was toxic at 10⁻⁴ M to the development after germination. Gibberellic acid promoted growth of cold treated turions even at 10⁻⁶ M. Indoleacetic acid at 10⁻⁴, 10⁻⁵ and 10⁻⁶ M induced outgrowth of both non-cold treated and cold treated turions. Apparently normal growth and development was observed in a high concentration of indoleacetic acid.     

Turion formation and behaviour inSpirodela polyrhiza at two levels of phosphate supply

The clone SJ ofSpirodela polyrhiza (L.) Schleiden forms turions under various nutritive conditions. As compared to 1500 μmol 1⁻¹ phosphate (P+), growth and frond yield of mixotropic cultures decreased, when 60 μol 1⁻¹ phosphate (P-) were available. By contrast, P-conditions increased the number, individual size, dry matter content, and total turion yield (mg turions per ml of the nutrient medium) of P-turions as compared to P+ ones. Germination behaviour of P-turions is characterized by fairly low zero levels in the controls, and by low heterogeneity in individual size as well as in the response patterns concerning the influence of light and/or phytoactive substances. P-turions from youngSpirodela cultures are extremely dormant. However, they undergo an after-ripening process if kept inside ageing cultures.     

Photophysiology of turion formation and germination inSpirodela polyrhiza

Standardized laboratory techniques for the vegetative growth of the duckweedSpirodela polyrhiza (Lemnaceaé), and for formation as well as germination of their turions were described. Increasing photon fluence rates of blue or red light increased the yield of turions. A specific stimulating effect of blue light was demonstrated under autotrophic but not under mixotrophic conditions. Therefore the spectral composition of light is not important in mixotrophic formation of turions whereas in autotrophic formation light sources with a higher portion of blue light are recommended. Dark-grown (etiolated) turions showed accelerated germination and higher germination percentage in comparison with light-grown turions after induction by a single red light pulse. This difference was overcome in continuous red light by speeding up the germination response of light-grown turions. Use of Petri dishes (8 cm³ nutrient solution) instead of Erlenmeyer flasks (50 cm³ nutrient solution) retarded germination response. Especially for long term experiments the use of Erlenmeyer flasks is recommended. Storage of turions for 72 h at 25 ‡C following at 5 ‡C in darkness after-ripening resulted in a decreased lag phase of the light-induced germination both after induction by a single light pulse and in continuous light. We thank Dr. Halina Gabrys, University of Crakow, Poland for critical discussion.     

Abscisic-acid-induced turion formation in Spirodela polyrrhiza L. I. Production and development of the turion

Abstract The production, growth, and development of the abscisic-acid-induced turion (a small dormant bud) of Spirodela polyrrhiza were investigated. Addition of ABA to a culture of S. polyrrhiza resulted in growth inhibition at concentrations as low as 10⁻⁶molm⁻³, growth being completely arrested at 10⁻² mol m. Over a single order of magnitude range around I0⁻⁴molm⁻³, ABA also induced the production of turions. The range of turion-producing concentrations of ABA was found to be much narrower than previously reported, turion production having a clearly defined threshold, optimum, and upper limit. The possibility that growth inhibition and turion formation are integrally linked aspects of a single response is discussed. Only primordia ≤0.7 mm long at the time of ABA addition could be induced to develop into turions and the events leading to turion formation were found to be reversible up to 72 h in ABA . It is concluded that in terms of turion formation there is a sensitivity window to abscisic acid lasting some 4–20h in the normal developmental life of frond cells. Providing cells experience the appropriate signal in this sensitivity window they initiate a new programme which eventually leads to turion formation. Microscopical analysis showed that the cells within this sensitivity window were still actively dividing. It is suggested that the developmental switch-over to rapid cell expansion and separation marks the end of this ABA sensitivity window.     

Undesirable side-effects of water hyacinth control in a shallow tropical reservoir

1. Based on a comprehensive data set collected monthly during 8 years (1997–2004), we evaluated the effects of mechanical removal of Eichhornia crassipes on the limnological characteristics and algal biomass of a polymictic shallow tropical reservoir. 2. Interrupted time series analyses indicated that the limnological responses to macrophyte removal can be classified as an ‘abrupt permanent impact’ implying that the overall mean of the time‐series shifted promptly after intervention. These analyses indicated a significant increase for pH, total phosphorus, total phytoplankton and cyanobacterial biomass, and a decrease in water transparency and CO₂ concentrations in the surface water; also, the increase in water stability, increase of bottom soluble reactive phosphorus (SRP) and decrease in bottom oxygen levels. 3. Cyclic anoxic periods previously observed during springs and summers were replaced by a persistent period of anoxic conditions in the sediment overlying water. Anoxic conditions were suitable for SRP release from sediments. Heavy cyanobacterial blooms became more persistent, maximum biomass (4229 mm³ L⁻¹) was 30 times larger, the blooms frequently reached 2 m and sometimes the bottom of the reservoir, contrasting to the preremoval period in which it reached at most 1 m deep. 4. The long‐term P dynamics in the system, initially driven by allochthonous nutrient loadings were replaced by internal ecological processes. Water hyacinth removal markedly accelerated the process of eutrophication due to internal feedback mechanisms, leading to a switch to a more turbid state. Biological feedback mechanisms were driven by cyanobacterial blooms by enhancing water stability, oxygen anoxia at the bottom and by increasing suitable conditions for P internal loading. These data support the hypothesis of the role of cyanobacterial blooms as an important factor impairing water quality and driving the ecosystem towards a stable degraded state. 5. These findings have important implications for the restoration of shallow stratifying eutrophic lakes, as the alternative degraded state is most likely to occur when compared with their non‐stratifying counterparts. Moreover, feedback mechanisms in tropical and subtropical shallow lakes seem to be stronger than in temperate ones, as stratification events are more likely to occur over the year, intensifying system resilience to restorative strategies.